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TRANSACTIONS
OF THE
EN TOMOnOGIC A SOC LEY
LONDON
THE
TRANSACTIONS
OF THE
ENTOMOLOGICAL SOCIETY
OF
LONDON
iD vey.
cary of Cong,
582404
se VULELEISI9
SV
LON DONE
SOLD AT THE SOCIETY’S ROOMS, 11, CHANDOS STREET
CAVENDISH SQUARE, W.,
AND BY LONGMANS, GREEN, AND CQ@.,
PATERNOSTER ROW, E.C. ; AND NEW YORK.
1918-1919.
DATES OF PUBLICATION IN PARTS.
Parts I, IL. (Trans., p. 1-230, Proc. i-xxxii) published 31 Dec., 1918
See Vac es 231 305,0n,
* V. —,, ¢lxxvil-cex) » 20 June, 1919
xxxili-elxxvi) ,, 29 Mar.,1919
ae
aL ne
ENTOMOLOGICAL SOCIETY OF LONDON
FouNDED, 1833.
INCORPORATED BY RoyYAL CHARTER, 1885,
PATRON: HIS MAJESTY THE KING.
OFFICERS and COUNCIL for the SESSION 1918-1919.
President,
Cre GAHAN MoAC Disc:
Wicc=Presioents,
H. ELTRINGHAM, M.A., D.Se.
ALBERT HUGH JONES.
S. A. NEAVE, M.A., D.Sc., F.Z.S.
Treasurer,
W. G. SHELDON.
Secretarics.
CommanpeR JAMES J. WALKER, M.A., R.N., F.L.S.
Toe Rev. GEORGE WHEELER, M.A., F.Z.S.
Librarian.
GEORGE CHARLES CHAMPION, F.ZS., /\AUESY
Otber Members of Council.
A. W. BACOT.
E. C. BEDWELL.
K. G. BLAIR, B.Sc.
Tes CEA PMVAN: M.D: F.Z.S.
W. C. CRAWLEY, B.A.
H. WILLOUGHBY ELLIS, F.Z.S.
J. C. EF; FRYER, M.A.
Tue Rev. F. D. MORICEH, M.A., F.Z.S.
H. E. PAGE.
Resident Librarian.
GEORGE BETHELL, F.R.Hi1st.8.
(Riatv ©)
Trustees of the Society.
PROF, W. BATESON.
HON. N. CHARLES ROTHSCHILD.
RT. HON. LORD WALSINGHAM.
Business and Publications Committee.
ROBERT ADKIN.
G. T. BETHUNE-BAKER.
JOHN HARTLEY DURRANT.
A. H JONES.
REV. F. D. MORICE.
And the Executive Officers of the Council.
British Mational Committee of Entomological Momenclature.
G. T. BETHUNE-BAKER. .
DR. CoS. GALEAIN:
DR..K. JORDAN.
LB eROUA.
REV. GEORGE WHEELER.
JOHN HARTLEY DURRANT, Secretary.
CONTENTS.
List of Fellows
Additions to the Library ...
List of Benefactions
III.
MEMOTIRS.
. Coleoptera of the families Ostomidae, Monotomidae, Colydiidae
and Wotiophyyidae from the Seychelles and Aldabra Islands.
By the late ANTOINE GROUVELLE. Communicated by HucH
Scott, M.A., F.L.S.
. New species of Staphylinidae from Singapore. Part I. By
Matcotm CaMEron, M.B., R.N., F.E.S.
Australian Braconidae in the British Museum. By Row1anp E.
TURNER, F.Z.S., F.E.S.
. On the naming of Local Races, Subspecies, Aberrations, Seasonal
Forms, etc. By Lorp Roruscuirp, F.R.S., ete.
. Molippa simillima, D.-Jones : A Correction. ake E. DUKINFIELD-
JONES, F.E.S.
. On Minicry in certain Butterflies of New Guinea. by Bee Ae
Drxey, M.A., M.D., F.BS.
An Instance of Mutation: Coccus viridis, Green, a Mutant from
Pulvinaria psidit, Maskell. By K,. Kunurt Kannan, M.A.,
. Some Remarks on Mr. Kunhi Kannan’s Paper, “An Instance of
Mutation.” By E. Ernest GREEN, F.Z.S.
IX. Observations on the Lepidopterous ee: Cossidae and on the
Classification of the ree oe . JEFFERIS TURNER,
MDS RSH. S. 2: ee .
X. The charina Group of Pinacopteryx. By F. A. Dixery, M.A.,
M.D., F.R.S., Subwarden of Wadham é ‘ollege, Oxford’
XI. Studies in Rhynchophora. IV. A preliminary note on the male
XIII.
genitalia. By Davip Suarp, M.A., F.R.S.
. Notes on the Ontogeny and Morphology of the male genital
tube in Coleoptera. By FrepEricx Muir, F.E.S.
New species of Staphylinidae from Singapore. Part IL By
Matcorm Cameron, M.B., R.N., F.E.S, nae ang
PAGE
ix
XXX
xlv
PAGE
118
130
149
x 4 vill)
PAGE
XIV. Notes on Australian Sawflies, especially the “ Authors’ Types”
and other specimens in the British Museum of Natural
History and the Hope Collections of the Oxford University
Museum; with diagnostic Synopses of the Genera and
Species, and photographs illustrating their structural
characters. By Francts Davip Moricr, M.A., F.Z.S. 2. 247
XV. The Hymenoptera of Fiji. By Rowianp E. Turner, F.Z.S.,
XVI. Notes on a large Heliconine collection made in French Guiana
in 1917, compared with a similar collection made in 1915.
By J. J. Joicry, F.H.S., and W. J. Kayr, F.E.8. ... een tO 4d
Proceedings for 1918 oe ie a xe nee ae .. 1-¢elxxix
Annual Meeting ... eee Ars Sue es oes aC des elxxx
Balance Sheet Se wes are see 308 Bae wes ae clxxxv
General Index = = we ace aes ae ae w= CIXXXvVii
Special Index nice ses 28 oa ae er fe eee excili
Errata re see ae aA ae eae aoe ae 460 ecx
EXPLANATION OF PLATES, TRANSACTIONS.
Plates I, II See page 57 Plate X See page 228
Plates III, 1V i 117 Plates XI-XV 3 327
Plates V-VIII * 148) Sketch Map 7 352.
Plate IX a 221
PROCEEDINGS.
Plate A. See page Ixxi.
Wist of Fellows
OF THE
ENTOMOLOGICAL SOCIETY OF LONDON.
HONORARY) FELLOWS.
Date of
Election.
1900 AuriviLitus, Professor Christopher, Stockholm.
1915 Brrwesn, Professor Antonio, via Romana, 19, Firenze, Italy.
1905 Bortvar, Ignacio, Museo nacional de Historia natural, Hipodromo,
17, Madrid.
1911 Comstock, Prof. J. H., Cornell University, Ithaca, New York, U.S.A.
1894 Foret, Professor Auguste, M.D., Yroune, Canton de Vaud,
‘Switzerland.
1898 Grassi, Professor Battista, The University, ome.
1915 Howarp, Dr. L. O., National Musewm, Washington, U.S.A.
1914 Lamegrre, Professor A., 74, rue Defasyi, Bruxelles.
1918 MarcHar, Dr. Paul, President of the Entomological Society of
France, 89, rue du Cherche-Midi, Paris.
1908 OBERTHUR, Charles, Rennes, Ille-et-Vilaine, France.
1913 Tran-SHanskl, A. P. Semenoff, Vassili Ostrov, 8 lin., 39, Petrograd,
Russia.
1911 Wasmany, Fr. Erich, 8.J., Valkenburg (L.) Ignatius Kolleg, Holland.
SPECIAL LIFE FELLOWS.
Date of
Election.
1916 (1894) Mratt, Louis Oompton, F.R.S., (Councin, 1908, 1908),
Norton Way N., Letchworth.
1916 (1888) YERBuURY, Colonel John W., late R.A., F.ZS., (Councit,
1896, 1903-5), 2, Ryder-street, St. James's, S.W.
ea
FELLOWS.
(The names of those who have not yet paid either the Entrance Fee or
the first year’s subscription are not included.)
Marked * have died during the year.
Marked + have compounded for their Annual Subscriptions.
Date of
Election
1914 + Aparr, E. W., B.A., Turf Club, Cairo, Egypt.
1913 Apams, B. G., 15, Fernshaw-road, Chelsea, S.W.
(eax y,)
1877 Apvams, Frederick Charlstrom, F.Z.S., 50, A shley-gardens, Victoria-
street, S.W. 1.
1902. ADKIN, Benaiah Whitley, Trenoweth, Hope-park, Bromley, Kent.
1885 ADKIN, Robert, (CounctL, 1901-2, 1911-13), Hodeslea, Meads,
Kastbourne.
1904 * Acar, E. A., La Haut, Dominica, B.W. Indies.
1912 Auten, J. W., M.A., 266, Wiliesden-lane, London, N.W. 2.
1911 Awnverson, T. J., Entomological Laboratory, Kabeti, Brit. HE. Africa.
1910 | ANDREwEs, H. E., 8, North Grove, Highgate, N.
1899 AnpReEws, Henry W., Shirley, Welling S.O., Kent.
1901 Awnnina, William, 39, Lime Street, B.C. 3.
1908 ANTRAM, Charles B., Somerdale Estate, Ootacamund, Nilgiri Hills,
S. India.
1913 ArmyvtacE, Edward O., Penrose, Millook, Powndstock, Bude.
1907 ARwNoxpD, G., M.Sc., A.R.C.S., Curator, Rhodesia Musewm, Bulawayo,
S. Africa.
1899 | Arrow, Gilbert J., (CouncrL, 1905-7), 9, Rossdale-road, Putney,
S.W. 15; and British Museum (Natural History), Cromwell-road,
SaWiul's
1911 Asnpy, Edward Bernard, 36, Bulstrode-road, Hounslow, Middlesex.
1907 + Asupy, Sidney R., 39, Park-lane, Wembley, Middlesex.
1886 Armorg, E. A., 48, High-street, King’s Lynn.
1913. Avinorr, André, Liteyny, 12, Petrograd, Russia.
1914 Awari, P. R., Medical Entomologist, c/o Grindlay & Co., Bankers,
26, Westmorland-street, Calcutta.
1901 Bacor, Arthur W., (Councit, 1916- ), York Cottage, York-hill,
Loughton, Essex.
1904 | BAGNALL, Richard 8., Penshaw Lodge, Penshaw, Durham.
1909 BaGweLu-PurReEFoy, Capt. Edward, Hast Farleigh, Maidstone.
1916 Batrour, Miss Alice, 4, Car/ton-gardens, 8.W., and Whittingehame,
Prestonkirk, Scotland.
1912 Batnarp, Edward, Govt. Entomologist, Agricultural College and
Research Institute, Coimbatore, Madras, S. India.
1886 Bankes, Eustace R., M.A.
1890 Barcuay, Francis H., F.G.8., Zhe Warren, Cromer.
1886 BarGAGui, Marchese Piero, Piazza S. Maria, Palazzo Tempi No. 1,
Florence, [taly.
1895 Barker, Cecil W., 81, Bellevue-road, Durban, Natal, South
Africa.
1902 Barraup, Philip J., Chester Cottage, Benhill-road, Sutton, Surrey.
1907 Barrverr, H. Frederick D., 1, Myrtle-road, Bournemouth.
1894 } Bareson, Prof. William, M.A., F.R.S., Fellow of St. John’s College,
Cambridge, The Manor House, Merton, Surrey.
1908 Bayrorp, E. G., 2, Rockingham-street, Barnsley.
1904 Bayne, Arthur F., c/o Messrs. Freeman, Custle-street, Framlingham,
Suffolk.
( xi)
1912 Baynes, Edward Stuart Augustus, 120, Warwick-street, Eceleston-
square, S.W. 1.
1896 | Beare, Prof. T. Hudson, B.Sc, F.R.S.E., (V.-Pres., 1910;
CounciL, 1909-11), 10, Regent Terrace, Edinburgh.
1908 Buck, Richard, Heckitt, The Park, Yeovil.
1905 Beprorp, The Duke of, K.G., Pres. Z.S., etc., Woburn Abbey, Beds.
1912 Beprorp, Gerald, Entomologist to the Union of South Africa,
Veterinary Bacteriological Laboratory, Ondestepoort, Pretoria,
Transvaal.
1913. Beprorp, Capt. Hugh Warren, Church Felles, Horley.
1899 Bepwett, Ernest C., (Councin, 1917- ), Bruggen, Brighton-road,
Coulsdon, Surrey.
1914. BenpderirTer, Eugéne, 11, Rue St. Jacques, Le Mans, France.
1904 bBrnersson, Simon, Ph.D., Lecturer, University of Lund, Sweden:
Curator, Entomological Collection of the University.
1915 Bennam, Prof. William Blaxland, M.A., D.Sc., F.R.S., University
of Otago, Dunedin, New Zealand.
1906 Bernraut, E. E., The Towers, Heybridge, Essex.
1913 Brst-Garpner, Charles C., Rookwood, Neath, Glamorgan.
1885 BrtTHune-BAKER, George T., F.L.S., F.Z.S., (Pres., 1913-14;
V.-Pres., 1910-11, 1915 ; Councit, 1895, 1910-15), 19, Clarendon-
road, Edgbaston, Birmingham.
1918 Brvertper, Col. W. W. O., C.B., D.S.0., R.A.M.C., c/o J. H.
Durrant, Esq., Natural History Museum, Cromuell-road, 8.
Kensington, S.W. 7.
1891 Buaper, W. H., F.L.S., 34, Cromwell-road, Hove, Brighton.
1904 Brack, James E., F.L.S., Nethereroft, Peebles.
1904 Buatr, Kenneth G., (Councrn, 1918— ), Claremont, 120, Sunning-
fields-road, Hardon, N.W. 4.
1885 Bratuwayt, Lt.-Col. Linley, F.L.S., Hagle House, Batheaston,
Bath.
1904 Butss, Maurice Frederick, M.R.C.S., L.R.C.P., 26 Woodville-
gardens, Ealing, W. 5.
1916 Bocock, Charles Hanslope, The Elms, Ashley, Newmarket.
1912. Bopxin, G. C., Govt. Entomologist, Georgetown, British Guiana.
1903 Boaur, W. A., The Bank House, Watchet.
1911 Botneau, H., 99, Rue de la Cote St. Thibault, Bois de Colombes,
Seine, France.
1891 Boorxu, George A., F.Z.S., M.B.O.U., The Hermitage, Kirkham,
Lanes.
1902 Bosrock, E. D., Oulton Cross, Stone, Staffs.
1913 Bowarer, Captain William, 20, Russell-road, Moseley, Birmingham.
1888 Bower, Benjamin A., Langley, Willow Grove, Chislehurst.
1894 + BowxEs, E. Augustus, M.A., Myddelton House, Waltham Cross.
1912 + Bowrtina, C. Talbot, Hoithow, Hainan, S. China.
1916 Box, Leonard Charles, F.R.H.S., Dominion Experimental Station,
Fredericton, New Brunswick,
(@ cite.)
1910 Boyp, A. Whitworth, The Alton, Altrincham, Cheshire.
1905 BrackEN, Charles W., B.A., 5, Carfrae Terrace, Lipson, Plymouth.
1917 Breer, Dr. H. G., Ph.D., Director of the Transvaal Museum,
Pretoria, Transvaal, S. Africa.
1904 BripGremMan, Commander The Hon. Richard O.B., R.N., 44, Lowndes-
square, S.W. 1; and e/o Commander-in-Chief, Cape of Good Hope
Station, c/o G.P.O.
1870 Briaes, Thomas Henry, M.A., Rock House, Lynmouth S.O., N. Devon.
1894. Bricut, Percy M., Cheriton, 26, Portchester-road, Bournemouth,
1909 Brirren, Harry, 22, Birch-qrove, Levenshulme, Manchester,
1902. Brovuanton, Major T. Delves, R.E., Mhow, India.
1878 Broun, Major Thomas, Chev. Legion of Honour, Mount Albert,
Auckland, New Zealand, -
1904. Brown, Henry H., Tower House, 8, Bruntsfiel€-terrace, Edinburgh.
1910 Browne, Horace B., M.A., Kenilworth, Scratcherd-lane, Morley,
Yorks.
1911 Brutzer, Rey. Henry W., Upton Vicarage, Peterborough.
1909 Bryant, Gilbert E., Fir Grove, Esher, Surrey.
1898 | BucHAN-Heprporn, Sir Archibald, Bart., J.P., D.L., Smeaton-
Hepburn, Prestonkirk.
1917 Bucxuiry, Dr. George Granville, M.D., F.S.A., Rye Croft South,
Manchester-road, Bury, Lancs.
1916 Buawnton, Prof. E., La Luciole, Aix-en-Provence, France.
1907 Botuerp, Arthur, F.S.A., Wimboro, Midsomer Norton, Somersetshire.
1896 + Burr, Malcolm, D.Sce., F.L.S., F.Z.8., F.G.S., A.R.S.M., (V.-PREs.,
1912; Counctn, 1908, 4, 1910-12), United University Club, Pall
Mall East, S.W.1.
1909 Burrows, The Rev. C. R. N., The Vicarage, Mucking, Stanford-le-
Hope, Essex.
1868 + Butter, Arthur G., Ph.D., F.L.S., F.Z.S., (Src., 1875; Councit,
1876), The Lilies, Beckenham-road, Beckenham.
1883. Butter, Edward Albert, B.A., B.Sc., (Councin, 1914-16), 14,
Drylands-road, Hornsey, N. 8.
1902 Burier, William E., Hayling House, Oxford-road, Reading.
1905 BurrEerFievp, Jas. A., B.Se., Ormesby, 21, Dorville-road, Lee, S.E.
1914 + BurreRFIELD, Rosse, Curator, Corporation Museum, Keighley, Yorks.
1912 + Buxron, Patrick Alfred, M.B.0.U., Fairhill, Tonbridge; and 40,
Cadogan Place, London, 8.W.
1904 Byart, Sir Horace A., K.C.M.G., B.A., Dar-es-Salaam, E. Africa.
1917 Cameron, Dr. Alfred E., M.A., D.Se., The Entomological Branch,
Department of Agriculture, Ottawa, Canada.
1902 Camerron, Malcolm, M.B., R.N., 7, Blessington-road, Lee, S.E.
1885 CampBELL, Francis Maule, F.LS., F.Z.8., ete., Brynllwydwyn,
Machynlleth, Montgomeryshire.
1898 CanprEzE, Léon, Mont St. Martin 75, Liége.
1880 CaNspDALE, W. D., Sunny Bank, South Norwood, 8.E. 25.
1889
1910
1892
1910
1895
1898
1915
1915
1911
1895
1912
1906
1900
( xiii)
Cant, A., 33, Festing-road, Putney, S.W.; and c/o Fredk. Du Cane
Godman, Esq., F.R.S., 45, Pont-street, S.W. 1.
CaruieR, E. Wace, M.D., F.R.S.E., Morningside, Granville-road,
Dorridge, and The University, Birmingham.
CARPENTER, The Honble. Mrs. Beatrice, 22, Grosvenor-road, S.W. 1.
CARPENTER, Geoffrey D. H., D.M., B.Ch., Uganda Medical Service,
Uganda Protectorate.
CarpPENtER, Prof. George H., B.A., B.Sc., Royal College of Science,
Dublin.
CARPENTER, J. H., Redcot, Belmont-road, Leatherhead,
Carr, Professor John Wesley, M.A., F.L.S., F.G.S., Professor of
Biology, University College, Nottingham.
Carr, William, B.Sc., Station-road, Bentham, Lancaster.
Carson, George Moffatt, Entomologist to the Government of New
Guinea, Port Moresby, Papua, vid Australia.
Carter, Sir Gilbert, K.C.M.G., Greycliffe, Lower Warberry-road,
Torquay.
Carter, Henry Francis, Assistant Lecturer and Demonstrator in
Medical and Economic Entomology, Liverpool School of Tropical
Medicine, University of Liverpool.
Carter, H. J., B.A., Garraiillah, Kintore-street, Wahroonga,
Sydney, N.S.W.
Carter, J. W., 15, Westfield-road, Heaton, Bradford.
1889 | Cave, Charles J. P., Ditcham Park, Petersfield.
1900
1871
1914
1891
1897
1913
1902
1889
1914
1909
1908
1914
1914
1908
CHAMBERLAIN, Neville, Westbowrne, Edgbaston, Birmingham.
Cuampion, George C., F.Z.8., A.L.S., Liprarian, 1891— (CouncIL,
1875-7); Heatherside, Horsell, Woking; and 45, Pont-street,
awed:
Cuampion, Harry George, B.A., Assistant Conservator of Forests,
W. Almora, U.P., India.
CHAPMAN, Thomas Algernon, M.D., F.R.S., F.Z.5., (V.-PRrEs., 1900,
1904-5, 1908, 1916-17; Councrn, 1898-1900, 1903-5, 1907-9,
1916-— ), Betula, Reigate.
CHAWNER, Miss Ethel F., Forest Bunk, Lyndhurst S.O., Hants.
CHEAVIN, Harold 8S. F.R.M.S., F.N.P.S., 70, Somerset-road,
Huddersfield.
CHEESMAN, E, M.
Curisty, William M., M.A., F.L.8., Watergate, Emsworth.
CarystaL, R. Neil, B.Sc., 277, First-avenue, Ottawa, Canada.
Cuark, Major C. Turner, F.Z.S., Hillerest, St. Augustine’s-avenue,
S. Croydon.
Cuiark, Edgar L., 34, Smith-street, Durban, Natal.
CiearE, L. D., Dept. of Science and Agriculture, Georgetown,
British Guiana.
CLEGHORN, Miss Maude Lina West, F.L.8., 14, Alipore-road,
Caleutta, India.
CLUTTERBUCK, Charles G., Heathside, 23, Heathville-road, Gloucester.
1908
1904
1917
1917
1914
1899
1906
1918
1913
1916
LS
1913
1895
1913
1909
1890
( xvas)
CiLurrerBucK, P. H., Indian Forest Department, Naini Tal, United
Provinces, India.
CockaYNE, Edward A., M.A., M.D., (Councin, 1915- ), 16, Cam-
bridge-square, London, W.2.
CockERELL, Prof. T. D. A., University of Colorado, Colorado,
U.S.A.
Cocks, Frederick, 26, Crown-street, Reading.
CoLEMAN, Leslie ©., Dept. of Agriculture, Bangalore, Mysore, India.
Cottin, James E., F.Z.S., (V.-Pres., 1913; Councin, 1904-6,
1913-15), Sussew Lodge, Newmarket.
CoLLINGE, Walter E., D.Sc. (St. And.), M.Se. (Birm.), F.LS.,
Research Fellow of the University of St. Andrews, The Gatty
Marine Laboratory, St. Andrews, Scotland.
Comstock, Dr. John Adams, c/o the South-Western Museum,
Marmion-way and Avenue, Los Angeles, California, U.S.A.
Conry, Miss Blanche A., The Poplars, Pucklechurch, Gloucestershire.
CornrorD, The Rey. Bruce, 13, Havelock-road, Portsmouth.
Corton, Sidney Howard, 14, Chesterfield-street, Mayfair, W. 1.
CowarpD, Thomas Alfred, F.Z.S., 36, George-street, Manchester.
CRABTREE, Benjamin Hill, Holly Bank, Alderley Edge, Cheshire.
Craaa, Capt. F. W., M.D., LMLS., c/o Messrs. Cox & Co,, Hornby-
road, Madras, India.
ne W.C., B.A., (Councit, 1917— ), 29, Holland Park-road,
W. 4.
CREWE, Sir Vauncey Harpur, Bart., Calke Abbey, Derbyshire.
1880 + Crisp, Sir Frank, LL.B., B.A., J.P.
1907
1908
1908
1901
1900
1886
1911
19138
1905
1912
1910
1903
1898
1913
1917
Crort, Edward Octavius, M.D., 12, North Hill-road, Headingley,
Leeds.
CuLPIN, Millais, M.B., F.R.C.S., Military Hospital, Ewell, Surrey.
Curtis, W. Parkinson, Drake North, Sandringham-road, Parkstone,
Dorset.
Dapp, Edward Martin.
DaueuisH, Andrew Adie, 7, Keir-street, Pollokshields, Glasgow.
Dannatt, Walter, St. Lawrence, Guibal-road, Lee, 8.E.
Davey, H. W., Inspector of Department of Agriculture, Melbourne,
Victoria, Australia.
Davinson, James, M.Sc., Highfield, Neston, Cheshire.
Davipson, James D., 32, Drumsheugh Gardens, Edinburgh.
Davis, Frederick Lionel, J.P., M.R.C.S., L.R.C.P., Belize, British
Honduras.
Dawson, William George, 44, London-road, Bromley, Kent.
Day, F. H., 26, Currock-terrace, Carlisle.
Day, G. O., Sahlatston, Duncan’s Station, Vancouver Island, British
Columbia. ,
Dickinson, Barnard Ormiston, B.A., Beech Hill, Newport, Salop.
DickskE, Arthur, 24, Lyford-road, Wandsworth Common, S.W. 18.
( xv )
1875 Distant, William Lucas, (V.-PREs., 1881, 1900; Src, 1878-
80; Councin, 1900-2), Glenside, 170, Birchanger-road, South
Norwood, 8.E. 25.
1887 Dixery, Frederick Augustus, M.A., M.D., F.R.S., Fellow and Bursar
of Wadham College, (PREs., 1909- 10; V.- Pa 1904-5, 1911;
CounciL, 1895, 1904-6), Wadham College, Oxford.
1909 ¢ Dopson, Thomas, 399, Plodder-lane, Farnworth, nr. Bolton.
1905 Dopp, Frederick P., Kuranda, vid Cairns, Queensland.
1912 Dora, Capt. Kenneth Alan Crawford, R.A.M.C., M.R.C.S., L.R.C.P.,
c/o Messrs. Holt & Co., 3, Whitehall-place, London, 8.W. 1.
1906 Dotuman, Hereward, Hove Howse, Newton-grove, Bedford-park,
W. 4.
1903 Doniman, J. C., Hove House, Newton-grove, Bedford-park, W. 4.
1906 Doncaster, Leonard, M.A., The University Musewm of Zoology,
Cambridge.
1891 DonisrHorpE, Horace St. John K., F.Z.S., (V.-Pres., 1911;
CounciL, 1899-1901, 1910-12), Dwrandesthorpe, 19, Hazlewwell-
road, Putney, 8.W. 15.
1913 Dow, Walter James, 5, Great College-street, Westminster, S.W. 1.
1910 Downes-Suaw, Rev. Archibald, Scotton Rectory, Gainsborough.
1884 Drucr, Hamilton H. C. J., F.Z.S., (Councit, 1903-5), Trefusis
Lodge, 3, Norfolk-road, N.W. 8.
1900 Drury, W. D., Clarendon, Laton-road, Hastings.
1894 Duparon, G. C., Director General of the me of Agriculture,
Meadi, Gu
1913. Durrrep, Charles Alban William, Stowting ay ‘tory, Hythe, and
Wye College, Kent.
1906 DuKINFIELD Jongs, E., Castro, Reigate.
1883 Durrant, John Hartley, (V.-PRmEs., 1912-13 ; CounciL, 1911-13),
Merton, 17, Burstock-road, Putney, 8S.W. 15; and British Musewm
(Natural History), Cromavell-road, South Kensington, S.W. 7.
1910 Eaues-Wuirr, Capt. J. Cushny, 49, Chester-terrace, Euton-square,
Sa Wealk
1912 Eart, Herbert L., M.A., 12, Avondale-road North, Southport, Lanes.
1865 Eaton, The Rev. Alfred Edwin, M.A., (Councit, 1877-9), Rich-
mond Villa, Northam S.O., N. Devon.
1902 Eprensren, Hubert M., The Elms, Forty Hill, Enfield, Middlesex.
1911 Epwarps, F. W., 56, Norton-road, Letchworth.
1886 Epwarps, James, Colesborne, Cheltenham.
1884 Epwarps, Stanley, F.L.8., F.Z.8., (Councin, 1912-14), 15, Sé.
Germans-place, Blackheath, S.E. 3.
1913. Epwarps, William H., Natural History Dept., The Museum,
Birmingham.
1916 ErraLatoun, Hassan, 34, Douglas Mansions, 120, Cromwwell-road,
Sante
1900 Enttorr, E. A., 16, Belsize Grove, Hampstead, N.W.
(_ =v ~)
1900 Enis, H. Willoughby, F.Z.S. (Counci, 1916- ), 3, Lancaster-
place, Belsize Park, N.W. 3.
1903 ExrrineHamM, Harry, M.A., D.Sc., F.Z.S., Vickz-PRESIDENT, (V.-
Pres., 1914; Councrn, 1913-15), Woodhouse, Stroud, Glowcester-
shire; and Hope Department, University Museum, Oxford.
1878 Enwes, Henry John, J.P., F.R.S., F.LS., F.Z.8., (PREs., 1893-4 ;
V.-PrEs., 1889-90, 1892, 1895 ; CouNcIL, 1888-90), Colesborne,
Cheltenham.
1914 * Emmett, Capt. Charles P., 1, High Cliff Villa, Felixstowe.
1903. ErneripGE, Robert, Curator, Australian Museum, Sydney, NSW.
1908 Evsracr, Eustace Mallabone, M.A., Wellington College, Berks.
1909 Evans, F. J., Calabar, Eastern Province, S. Nigeria.
1917 * FarquHarson, Charles Ogilvie, M.A., B.Sc., Moor Plantation,
Ibadan, Nigeria.
1907. FrarHer, Walter, Kibwezi, British Hast Africa.
1900 Ferentrnam, H. L. L., Mercantile Buildings, Siwmmonds-street,
Johannesburg, Transvaal.
1861 Frnn, Charles, Hversden House, Burnt Ash Hill, Lee, S.E. 12.
1910 Frnyrs, A., M.D., 170, North Grange Grove-Avenue, Pasadena,
California, U.S.A.
1918 Frrauson, Anderson, 22, Polworth-gardens, Glasgow, W.
1889 FERNALD, Prof.C. H., c/o H.T. Fernald, Esq., Amherst, Mass., U.S.A.
1900 Frrra, J. Digby, F.L.S., Boys’ Modern School, Leeds.
1900 FrLemyna, The Rev. Canon W. Westropp, M.A., Coolfin, Portlaw, co.
Waterford.
1898 Friercuer, T. Bainbrigge, R.N., Agricultwral Research Institute,
Pusa, Bihar, India.
1883 + FLercHErR, William Holland B., M.A., Aldwick Manor, Bognor.
1905 FLorrsHErM, Cecil, 16, Kensington Court Mansions, 8.W.
1885 Foxksr, A. J. F., Zierikzee, Zeeland, Netherlands,
1914 ForpHam, William John, M.R.C.S., L.R.C.P., The Villa, Bubwith,
Selby, Yorks.
1913 Foster, Arthur H., M.R.C.S., L.R.C.P.(Eng.), M.B.0.U., Sussex
House, Hitchin, Herts.
1900 Founkrs, P. Hedworth, B.Sc., Harper-Adams Agricultural College,
Newport, Salpp.
1898 Founrarne, Miss Margaret, 1727, Wilcox-avenue, Los Angeles,
California, U.S.A.
1880 Fownrer, The Rev. Canon, D.Sc., M.A., F.L.S., (PReEs., 1901-2 ;
V.-Pres., 1903 ; Sec., 1886-96), Harley Vicarage, near Reading.
1908 Fraser, Frederick C., Capt., M.D., I.MLS., Government Maternity
Hospital, Madras, India.
1896 Frexkn, Perey Evans, Southpoint, Limes-road, Folkestone.
1888 Fremurn, H. Stuart, M.R.C.S., L.R.C.P., Markwith, Nether-street,
North Finchley.
1910 Frispy, G. E., 31, Darnley-roud, Gravesend,
(Gaexvily 6)
1908 Froaearr, Walter W., F.L.S., Government Entomologist, Agri-
cultural Museum, George-street North, Sydney, New South Wales.
1891 FRronawk, F. W., Uplands, Thundersby, Essex.
1906 } Fry, Harold Armstrong, P.O. Box 46, Johunnesburg, Transvaal Colony.
1900 Fryer, H. Fortescue, The Priory, Chatteris, Cambs.
1907 FrvyEr, John Claud Fortescue, M.A., (Councin, 1916- ), Board
of Agriculture and Fisheries, Northumberland-avenue, W.C, 2.
1876 Funier, The Rev. Alfred, M.A., The Lodge, 7, Sydenham-hill,
Sydenham, S.E. 26.
1898 Funnier, Claude, Government Entomologist, Pietermaritzburg,
Natal.
1887 Gauwan, Charles Joseph, M.A., D.Sc., PRESIDENT, (V.-PREs., 1916 ;
SEc., 1899-1900 ; Councin, 1893-5, 1901, 1914- ), 8, Lonsdale-
road, Bedford Park, W. 4; and British Museum (Natural
History), Cromell-road, S.W. 7.
1890 Garpner, John, Lawrel Lodge, Hart, West Hartlepool.
1901 | GarpnER, Willoughby, F.L.S., F.S.A., Deqgunwy, N. Wales.
1913 bE Gays, J. A., 1, Castletown Mansions, 3, Castletown-road, W.
Kensington, W.14 3; and King’s College, Lagos, 8S. Nigeria.
1899 GeELpART, William Martin, M.A., 10, Chadlington-road, Oxford.
1913 Guise, Lachlan, 38, Blackheath Park, Blackheath, S.E. 3.
1915 Gipson, Arthur, Entomological Branch, Dept. of Agriculture,
Ottawa, Canada,
1908 GrFrarRD, Walter M., P.O. Bow 308, Honolulu, Hawaii.
1907 GuinEs, Henry Murray, Head Keeper of Zoological Gardens, Scuth
Perth, W. Australia.
1904 Ginuiar, Francis, B.A., Windham Club, St. James’s-square,
Piccadilly, S.W. 1.
1914 Goprrey, E. J., Education Dept., Bangkok, Siam.
1865 | GopMAN,. Frederick Du Cane, D.C.L., F.R.S., F.L.S., F.Z.S., (PREs.,
1891-2; V.-Pres., 1882-3, 1886, 1889-90, 1902; Councrn, 1880-
1, 1900), South Lodge, Lower Beeding, Horsham; and 45, Pont-
street, SW.
1904 Goopwin, Edward, Canon Court, Wateringbury, Kent.
1898 Gorpon, J.G. McH., Corsemalzie, Whauphill S.O., Wigtownshire.
1898 Gorpon, R. 8. G. MeH., Drumblair, Inverness.
1855 Goruam, The Rev. Henry Stephen, I°.Z.8., (Councrn, 1882-3), High-
croft, Great Malvern.
1913 Goueu, Lewis, Ph.D., Entomologist to the Govt. of Egypt, Dept. of
Agriculture, Cuiro.
1909 _Gowbry, Carlton C., B.Se., Biological Laboratory, P.O. Box, 5,
Kampala, Uganda, E. Africa.
1918 Grack, George, B.Sc., A.R.C.Sc., Inglenool, Utley, Keighley, Yorks
1914 Grave ey, F. H., The Indian Musewm, Caleutta.
1911 Graves, Capt. P. P., Turf Club, Cairo, Egypt.
( xviii )
1891 | Green, E. Ernest, F.Z.S., (V.-PrEs., 1915; Councit, 1914-16),
1910
1894
Ways End, Beech avenue, Camberley.
GREEN, Herbert A., The Central Fire Station, Durban, Natal.
GREEN, J. F., F.Z.S., 49, Victoria-road, Kensington, W. 8.
1893 + Greenwoop, Henry Powys, F.L.S., Whitsbury House, Salisbury.
1888
1894
1905
1906
1910
1912
1906
Grirritns, G. C., F.Z.S., Penhurst, 3, Leigh-road, Clifton, Bristol.
Grimsuaw, Perey H., Royal Scottish Museum, Edinburgh.
Grist, Charles J., The Croft, Curol Green, Berkswill, Coventry.
Gurney, Gerard H., Keswick Hall, Norwich.
Gurney, William B., Asst. Govt. Entomologist, Department of
Agriculture, Sydney, Australia.
Hacker, Henry, Butterfield-street, Bowen Bridge-road, Brisbane,
Queensland,
Haut, Arthur, 7, Park-lane-mansions, Croydon.
1890 + Haut, Albert Ernest, c/o City Librarian, Surrey-street, Sheffield.
1885
1912
1898
1915
1891
Haut, Thomas William, Ardestie, Stution-road, Chorley Wood,
Flerts.
Hawtiert, Howard Mountjoy, 64, Westbowrne-road, Penarth,
rlamorganshire.
Hamuyn-Harris, R., D.Sc., F.L.S., F.Z.S., F.R.M.S., Director of the
Queensland Museum, St. Ronans, Wilston, Brisbane, Australia.
Hamm, Albert Harry, 22, Southfield-road, Oxford.
Hanpury, Frederick J., F.L.S., Brockhurst, E. Grinstead.
1905 + Hancock, Joseph L., 5454, University-avenue, Chicago, U.S.A.
1916
1917
1903
1904
1910
1910
Hannyneton, Frank, c/o Messrs. Parry & Co., Madras, India.
Harpinea, William G., F.L.S., F.R.C.L., Christ Church, Oxford.
Hark, E. J., 4, New-square, Lincoln's Inn, W.C. 2.
Harris, Edward, 58, Wilson-street, Finsbury, E.C.
Harwoop, Philip Bernard, 2, Fern Villas, Melford-road, Sudbury.
HawkKsHaw, J. C.
1913 +} HawKsuHaw, Oliver, 3, Hill-street, Mayfair, W. 1.-
1910
1910
1898
1918
1903
1908
1913
1913
Hepces, Alfred van der, Stoke House, Stoke Mandeville, Bucks.
HENDERSON, J., c/o Messrs. Osborne & Chappel, Ipoh, Perak,
Federated Malay States.
Heron, Francis A., B.A., 9, Park House, Highbury Park, N. 5.
HerRoD-HEMPSALL, Joseph, Orchard House, Stockingstone-road,
Luton, Beds.
Herrrop-Hempsatt, William, W.B.C. Apiary, Old Bedford-road,
Luton, Beds.
Hewirr, C. Gordon, D.Se., Dominion Entomologist, Dept. of
Agriculture, Ottawa, Canada.
Hewitt, John, B.A., Director, Albany Museum, Grahamstown,
S. Africa.
Hitt, Gerald F., Entomologist to the Australian Institute of
Tropical Medicine, Townsville, N. Queensland, Australia.
1876 + HittMan, Thomas Stanton, Hastgate-street, Lewes.
1907
1917
1914
1912
1888
1902
1910
1887
1898
1910
1901
1897
1903
(h Bab ca)
Hoar, Thomas Frank Partridge, Mercia, Albany-road, Leighton
Buzzard.
Hockin, John W., Castle-street, Launceston.
Honan, The Rev. Prebendary Edward Grose, The Vicarage, Pad-
dington, W. 2.
Hooper, Harold, St. James’ Mansions, 54, Piccadilly, W.
Hopson, The Rev. J. H., B.A., B.D., Rhyddington, Clifton Drive,
Lytham.
Hote, R.8., c/o Messrs. King and Co., Bombay.
Ho.rorp, H. O., Elstead Lodge, Godalming, Surrey.
Houtuanp, The Rev. W. J., D.D., Ph.D., Carnegie Museum,
Pittsburgh, Penn., U.S.A.
Hoitman-Hunt, C. B., Asst. Entomologist, Department of Agri-
culture, Kuala Lumpur, Federated Malay States.
Hoimes, Edward Morrell, Ruthven, Sevenoaks.
Horson, Montagu F., L.D.S., R.C.S.Eng., F.L.S.,7, Harley- street, W. 1.
Horne, Arthur, Bonn-na-coile, Murtle, Aberdeenshire.
Hovueuron, J. T., 1, Portland-place, Worksop.
1907 + Howarp, C. W., Canton Christian College, Canton, China.
1900
1907
Howes, W. George, 432, George-street, Dunedin, New Zealand.
Howtert, Frank M., M.A., Wymondham, Norfolk.
1865 | Hupp, A. E., 108, Pembroke-road, Clifton, Bristol.
1888
1907
1912
L917,
1897
Hupson, George Vernon, Hill View, Karori, Wellington, New Zealand.
Huenes, C. N., 178, Clarence Gate-gardens, Regents Park, N.W. 1.
Hug, Miss Lily, Hollywood, Colinton-road, Edinburgh.
ITunrer, David, M.A., M.B., The Coppice, Nottingham.
ImaGe, Prof. Selwyn, M.A., (Councin, 1909-11), 78, Parkhurst-road,
Camden-road, N. 7.
1912 Imus, A. D., D.Sc, M.A. F.LS., Rothamstead Experimental
1908
1918
1907
1917
1907
HOW
1910
1914
1869
1898
Station, Harpenden, Herts.
Irby, Col. Leonard Paul, Evington-place, Ashford, Kent.
Tsaacs, P. V., Assistant Entomologist, Madras Agricultural College
and Research Institute, Coimbatore, India.
Jack, Rupert Wellstood, Government Entomologist, Department
of Agriculture, Salisbury, Rhodesia.
Jackson, Miss Dorothy J., Swordale, Evanton, Ross-shire.
Jackson, P. H., 112, Balham-park-road, 8.W. 12.
Jacoss, Major J. J., R.E., Holmesleigh, Burgess Hill, Sussex.
Jacoss, Lionel L., c/o Algoma Steel Corporation, Sault Ste. Marie,
Ontario, Canada. :
JANsE, A. J. T., Lst-street, Gezina, Pretoria, S. Africa.
JANSON, Oliver E., 44, Great Russell-street, Bloomsbury, W.C. 1. ;
and Cestria, Claremont-road, Highgate, N. 6.
JANSON, Oliver J., Cestria, Claremont-road, Highgate, N. 6.
( xx )
1912. Jarpine, Nigel K., Summerhill House, Willesborough, nr. Ashford,
Kent.
1912 * Jemmert, C., Withersdane House, Wye, Kent.
1886 JENNER, James Herbert Augustus, Hast Gate House, Lewes.
1909 JEpson, Frank P., Department of Agriculture, Suva, Fiji Islands.
1917 Jermyn, Col. Turenne, Highcliffe, Weston-super-Mare.
1886 JoHn, Evan, Llantrisant S.0., Glamorganshire.
1907 Jounson, Charles Fielding, West Bank, Didsbury-road, Heaton
Mersey.
1917 JOHNSON, Jesse, 16 and 17, Jarston-road, Stafford.
1889 Jounson, The Rev. W. F., M.A., Acton J/iectory, Poyntz Pass,
co. Armagh.
1908 Jorcry, James J., The Hill, Witley, Surrey.
1888 Jones, Albert H., Vick-PRestDENt, (V.-PREs., 1912; Treas., 1904—
17 ; CounctL, 1898-1900), Shrublands, Eltham, SE.
1894} Jorpan, Dr. K., (V.-Pres., 1909; Councrn, 1909-11), The
Museum, Tring.
1910 JosrpnH, E. G., 238, Clanricarde-gardens, W. 2.
1910 Joy, Ernest Cooper, Eversley, Dale-road, Purley.
1902 Joy, Norman H., M.R.C.S., L.R.C.P., Theale, Berks.
1911 Kannan, Kunhi, M.A., Asst. Entomologist to the Govt. of Mysore,
Bangalore, South India.
1876 | Kay, John Dunning, Leeds.
1896 | Kaye, William James, (CounciL, 1906-8), Caracas, Ditton Hull,
Surbiton.
1907 Krtxiy, Albert Ernest McClure, Division of Entomology, Department
of Agriculture, Pretoria, S. Africa.
1890 Kenrick, Sir George H., Whetstone, Somerset-road, Edgbaston,
Birmingham. ;
1904 KersHaw, G. Bertram, Ingleside, West Wickham, Kent.
1906 Keynes, John Neville, M.A., D.Sc., 6, Harvey-road, Cambridye.
1900 Krys, James H., 7, Whimple-street, Plymouth.
1912 Kine, Harold H., Govt. Entomologist, Gordon College, Khartoum,
Sudan.
1889 Kuna, Prof. James J. F.-X., 1, Athole Gardens-terrace, Kelvinside,
Glasgow.
1913 Kirey, W. Egmont, M.D., Hilden, 46, Sutton Court-road, Chiswick,
W. 4,
1917 Kirxparrick, Thos. W., The Deanery, Ely, and Room 270, War
Office, Whitehall, S.W.1.
1887 | Kunin, Sydney [T, F.L8., F.R.AS., Hatherlow, Raglan-road,
Reigate.
1916 Larne, Frederick, Natural History Musewm, Cromwell-road, 8.W. 7,
1910 Laxrin, C. Ernest, M.D., F.R.C.S., 2, Park-crescent, Portland-
place, W. 1
(a xi"
1911 ¢ Lamgorn, W. A., M.R.C.S., L.R.C.P., Zomba, Nyasuland, E. Africa,
1917 Lanenam, Sir Charles, Bart., Tempo Manor, Co. Fermanagh.
1916 Larra, Prof. Robert, D.Phil., University of Glasgow.
1912 Larour, Cyril Engelhart, Port of Spain, Trinidad, British West
Indies.
1895 Larrer, Oswald H., M.A., Charterhouse, Godalming.
1899 Lua, Arthur M., Government Entomologist, Musewm, Adelaide,
S. Australia.
1914 LercuMan, Alleyne, M.A., F.L.S., F.C.S., Corpus Christi College,
Oxford ; and St. Hubert’s, Main-street, Georgetown, British Guiana.
1910 Leien, H.S8., The University, Manchester.
1900 LriaH-Puriiips, Rev. W. J., Burtle Vicarage, Bridgwater.
1903 ¢ Levert, The Rev. Thomas Prinsep, Frenchgate, Richmond, Yorks.
1876 Lewis, George, F.L.S8., (CounctL, 1878, 1884), 30, Shorneliffe-road,
Folkestone.
1908 + Lewis, John Spedan, Grove Farm, Greenford Green, South Harrow ;
and 277, Oxford-stret, W.
1892 Licutroor, R. M., South African Museum, Cape Town, Cape of
rood Hope.
1914 Lister, J. J., St. John’s College, Cambridge; and Merton House,
Grantchester, Cambs.
1903. Lirrnrer, Frank M., Bow 114, P.O., Launceston, Tasmania.
1865 | Lizwetyy, Sir John Talbot Dillwyn, Bart, M.A. F.LS.,
Peullergare, Siwansea,
1881 + Luoyp, Alfred, F.C.S., Zhe Dome, Bognor.
1885 ¢ Luoyp, Robert Wylie, (Councrn, 1900-1), I, 5 and 6, Albany,
Piccadilly, W. 1.
1903 Lorrnousg, Thomas Ashton, The Croft, Linthorpe, Middlesbrowyh.
1908 Lonespon, D., The Flower House, Southend, Catford, S.E. 6.
1904} Lonestarr, George Blundell, M.A., M.D., (V.-Prus., 1909, 1915,
1917 ; Councin, 1907-9, 1915-17), Highlands, Putney Heath,
S.W. 15.
1899 Lounspury, Charles P., B.Se., Government Entomologist, Bow 513,
Pretoria, S. Africa.
1894 * Lowe, The Rev, Frank E., St. Stephen’s Vicarage, Guernsey.
1893 Lower, Oswald B., Pinurro, South Australia.
1901 Lower, Rupert S8., Argent-street, Broken Hill, New South Wales.
1898 Lucas, William John, B.A., (Counctn, 1904-6), 28, Knight’s Park,
Kingston-on- Thames.
1903. LygEtn, G., Gisborne, Victoria, Australia.
1912 Lyx, George Trevor, Mayfield, Linsfield-road, Cambridge.
1909 Lyon, Francis Hamilton, 89, Clarence Gate-qardens, Upper Baker-
street, N.W. 1.
1887 M‘Doueatt, James Thomas, St. Lawrence, Isle of Wight.
1910 Macpoueat1,R. Stewart, M.A.,D.Sc., F.R.S.E., Edinburgh University.
1900 Mackwoop, The Hon. F. M., M.L.C., Colombo, Ceylon.
( xxii)
1899 + Matn, Hugh, B.Sec., (Councin, 1908-10), Almondale, Buckingham-
1914
1905
1892
road, South Woodford, N.E.
Matuock, J. Russell, State Entomologist’s Office, Urbana, Illinois,
U.S.A.
Matty, Charles Wm., M.Sc., Dept. of Agriculture, Cape Town,
S. Africa.
Manssrina@k, William, 4, Norwich-road, Wavertree, Liverpool.
1894 + Marsuatt, Alick.
1895
1896
1897
1895
1865
1887
1912
1900
1916
1913
1885
1907
1914
1887
1912
1880
1883
1913
1905
1914
1918
1879
1902
1899
1916
1886
MARSHALL, Guy Anstruther Knox, D.Sc., F.Z.S., (CounciL, 1907-8),
6, Chester-place, Hyde Park-square, W. 2.
MarRsHALL, P., M.A., B.Sc. F.G.S., University School of Mines,
Dunedin, New Zealand.
Martineau, Alfred H., Barum, Crewkerne, Somerset.
Massey, Herbert, Lvy-Lea, Burnage, Didsbiry, Manchester.
MatHEW, Gervase F., F.L.S., Paymaster-in-chief, R.N., (CoUNCIL
1887), Lee House, Dovercourt, Harwich.
MarrHews, Coryndon, Stentuway, Plymstock, S. Devon.
MAULIK, Samarenda, 211, Piccadilly, W.
Maxwett-Lerroy, H., Imperial College of Science and Technology,
South Kensington, S.W.
May, Harry Haden, Blackfriars House, Plymouth.
MeaveEn, Louis, Melbowrne, Dyke-road, Preston, Brighton.
MELVILL, James Cosmo, M.A., F'.L.8., Meole Brace Hall, Shrewsbury.
MELVILLE, Mrs. Catharine Maria, Redvers, Essa-road, Saltash.
Menon, J. R., B.A., Trichur, Cochin State, S. India.
MERRIFIELD Frederic, (PREs., 1905-6 ; V.-PReEs., 1893, 1907 ; SEc..
1897-8 ; CouNcIL, 1894, 1899), 14, Clifton-terrace, Brighton.
Mercatre, Rev. J. W., The Vicarage, Ottery St. Mary, Devon.
Meyrick, Edward, B.A., F.RS., F.Z.S., Thornhanger, Marlborough.
Mines, W. H., ¢/o E. Step, Esq., 158, Dora-road, Wimbledon Park,
S.W. 19.
Miter, F. V. Bruce, Livingston, N. Rhodesia, Africa.
Mirrorp, Robert Sidney, C.B., Thornlea, Weybridge.
Miyake, Dr. Tsunekata, The Agricultural Colleae, Tokyo Imperial
University, Komaba, Tokyo, Japan.
Monro, Lieut. James W., R.A.M.C., 2nd Sanitary Coy., Duke of
York’s Head Quarters, Chelsea, S.W.
Monverro, Dr. Antonio Augusto de Carvalho, 70, Rua do Alecrinar,
Lisbon.
Monrcomery, Arthur Meadows, 34, Shalimar Gardens, Pembridge-
road, North Acton, W. 11.
Moore, Harry, 12, Lower-road, Rotherhithe.
Moore, Ralph Headley, B.A., Heathfield, Plymstock, Devon.
Morean, A. C. F., F.LS., 185, Oakwood-court, Kensington, W. 14.
1889 + Morice, The Rev. F. D., M.A., F.Z.S., Fellow of Queen’s College,
Oxford, (PREs., 1911, 1912, V.-PRrEs., 1902, 1904, 1913; CounciL,
1902-4), Brunswick, Mount Hermon, Woking.
(2) xxii 33
1895 + Mortey, Claude, F.Z.S., Monk Soham House, Suffolk.
1893 Morron, Kenneth J., 13, Blackford-road, Edinburgh.
1910 Moseny, Martin E., 94, Campden Hill-road, Kensington, W.
1882 Mostey, 8. L., The Musewm and Technical College, Huddersfield.
1911 Moss, Rev. A. Miles, c/o Messrs. Booth & Co., Para, Brazil.
1907 ¢ Moutton, Capt. John C., M.A., B.Sc, F.LS., F. ZS;, &e; 4th
Wiltshire Regt., Fort Sinan Singapore, and The Hall,
Bradford-on- Avon.
1911 Movunsey, J. Jackson, 24, Glencairn-crescent, Edinburgh.
1901 + Muir, Frederick, H.S.P.A. Haperiment Station, Honolulu, Oahu,
ETeeTe
1912 ¢ Muttay, Jal Phirozshah, M.A., F.L.S., F.Z.S., Professor of Biology,
St. Xavier’s College, Lamington-road, Grant Road Post, Bombay,
India.
1869 + Méuuer, Albert, F.R.G.S., (Counctn, 1872-3), c/o Herr A. Miiller-
Mechel: Gea zachori nese 60, Basle, Switzerland.
1914. Murray, George H., Government Station, Kikori, Detta Division,
Papua,
1917 Muscuamp, Perey A. H., Charterhouse School, Godalming.
1909 MusHam, John F., 48, Bronte street, Selby, Yorks.
19038 Neave, 8S. A., M.A., D.Se., F.Z.S., Vick-Presipent, (CoUNCIL,
1916— ), Imperial Bureau of Entomology, 89, Queen's Gate,
Kensington, 8.W.7 ; and 24, de Vere-gardens, Kensington, W.8.
1901 Nevinson, E. B., Morland, Cobham, Surrey.
1907 Newman, Leonard Woods, Bexley, Kent.
1913 Newman, Leslie John William, Bernard-street, Claremont,
W. Australia.
1909 NewsrxHaD, Alfred, The Grosvenor Musewm, Chester.
1890 NewsteaD, Prof. Robert, M.Sc., F.R.S., A.L.S., Hon. F.R.HLS.,
Dutton Memorial Professor of Entomology, The School of Tropical
Medicine, University of Liverpool.
1914. Nicuoison, Charles, 35, The Avenue, Hale-end, Chingford, E. 4.
1909 NicHotson, Gilbert W., M.A., M.D., (Councrn, 1913-15), Oxford
and Cambridge Club, Pall Mall, 8.W. 1.
1918 Nuimmy, Ernest Willian, 210, Whippendell-road, Watford, Herts.
1906 NIx, ohn Ashburner, Pacate Crawley, Sussex,
1916 Nouira, Akio, Tener Otagiqun, Kyoto, Japan.
1914 Norris, Frederic de la Mare, The Agricultural Department, Kuala
Lumpur, Federated Malay States,
1915 Norrucorr, Dr. A. B., Blenheim House, Monkgate, York.
1878 Norrmer, Thomas, Ashford, Kent.
1895 Nurss, Lt.-Colonel C. G., 145, Beaufort-street, Chelsea, S.W. 3
1877 OperTHiR, René, Rennes (Ille-et-Vilaine), France.
1893 + OaLx, Bertram 8., Steeple Aston, Oafordshire.
1910 OnpaKeER, Francis A,, M.A,, The Red House, Haslemere.
(_ xxiv)
1918 O’Netn, Rev. Fr., S.J., Salisbury, Rhodesia.
1913 ORMISTON, Walters Kalupahani, Haldummaulle, Ceylon.
1895 Paar, Herbert E., (Counetn, 1918- ), Bertrose, Gellatly-road, St.
Catherine’s Park, S.K. 15.
1916. Patmer, Arthur Raymond, Ingleholme, Norton Way, Letchworth,
Herts.
1918 Parris, R. Stanway, 6 High-street, Bishop's Stortford.
1918 Parsons, Dr. Allan Chilcott, M.R.C.S., L.R.C:P., D.Ph., etc.,
School of Army Sanitation, Aldershot.
1912 Parerson, Edward J., Fairholme, Crowborough.
1913. Pracock, Alexander David, Armstrong Colleye, Newcastle-on-Tyne..
1911 Prarson, Douglas, Chilivell House, Chilivell, Notts.
1916 Prrepies, Howard M., 13, Chesham-street, S.W. 1
1915 Prine, Major Harry Diamond, I.M.S., c/o Alliance Bank of Sind,
Peshawar, India.
1914. PenpLeBury, Major Wm. J. von Monté, Broadlands, Shrewsbury,
and Keble College, Oxford.
1883 Psrincury, Louis, D.Sc., F.Z.S., Direetor, South African Museum,
Cape Town, South Africa.
1903 + Perkins, R. C. L., M.A., D.Se., F.Z.S., Park Hill House, Paignton,
Devon ;. and Board of Agriculture, Division of Entomology,
Honolulu, Hawaii.
1907 + Perrins, J. A. D., 3rd Seaforth Highlanders, Davenham, Malvern.
1897 Puiniips, Capt. prabert C., M.R.C.S., L.S.A., 17, Hereford-road,
Bayswater, W. 2.
1903 ¢{ Prittirs, Montagu A., F.R.G.S., F.Z.S., Detonanoe Howse Prepara-
tory School, eights.
1917 Prckarp-CampBrinGE, Arthur D., M.A., Balliol College, Oxford.
1891 Prerce, Frank Nelson, 1, Zhe Elms, Dingle, Liverpool.
1903 * PrncnErR, Col. Jesse George, I.M.S., F.R.C.S., 133, Gloucester-road,
Kensington, S.W. 7.
1913. Prarr, Ernest Edward, 403, Essenivood-road, Durban, Natal.
1885 Pou, J. R. H. Neerwort van der, Poste restate, Geneva, Switzer-
land.
1870 | Porritt, Geo. T., F.L.S., (Councin, 1887), Hlm Lea, Dalton,
Huddersjield.
1884 + Pout ON, Professor Edward B., D.Sc., M.A., F.R.S., F.L.S., F.G.S
F.Z.8., Hope Professor of Congas in the igersity atl Oxiorde
(eae 1903-4; V.-Pres., 1894-5, 1902, 1905 ; CounciL, 1886- 8.
1892, 1896, 1905-7), Wykeham Ilouse, Bajbiny rod, Oxford.
1905 Power, Harold, 7, Rue Mireille, Hyéres (Var), France.
1908 Prarr, William B., 10, Lion Gate Gardens, Richmond, Surrey.
1878 Prick, David, 48, West-street, Horsham.
1908 Pripraux aRaner: M., (Counctn, 1917), Woodlands, Brasted Chart,
Sdn y
1904 Priskn, Richard A. R., 9, Melbourne Avenue, West Ealing.
~ ememase
ee
(7 exocy) 99)
1893 Prout, Louis Beethoven, (Counctn, 1905-7), 84, Albert-roud,
Dalston, E. 8.
1910 Punnett, Professor Reginald Crundall, M.A., Caius College,
Cambridge.
1900 Rartnsow, William J., The Australian Museum, Syduey, NSW,
1912) Rair-Smira, W., Hollybrook, Rose Heyiworth-road, Abertillery,
Monmouthshire.
1914 Ramaxrisuna, Aiyar, T. V., B.A., F.Z.S.,° The Agricultural
College, Coimbatore, S. India.
1918) Rao, H. Ananthaswamy, Curator of the Govrnwment Museum,
Bangalore, India.
1916 Rao, Yelseti Ramachandra, M.A., c/o Imperial Entomologist,
Pusa, Behar, India.
1907 Raywarp, Arthur Leslie, 91 and 93, Southwark-street, S.E. 1.
1898 Reurer, Professor Enzio, Helsingfors, Finland.
1910 be Ru&-Puiuier, G. W. V., Chief Examiner of Accounts, North-
Western Ry., Abbott-road, Lahore, India.
1912 Riney, Norman Denbigh, 94, Drakefield-road, Upper Tooting, S.W.17;
and British Museum (Natural History), S. Kensington, S.W. 7.
1908 Rrrpon, Claude, M.A., 28, Walton-street, Oxford
1917 Roperts, A. W. Rymer, M.A., Rothamsted Experimental Station,
Harpenden
1905 Ropinson, Herbert C., Curator of State Museum, Kuala Liampwur,
Selangor.
1904 Roprnson, Lady, Worksop Manor, Notts.
1869 | Ropinson-Doucuias, William Douglas, M.A., F.L.S.
Orchardton, Castle Douglas.
1908 Roaers, The Rev. K. St. Aubyn, M.A., Church Missionary Society,
Mombasa, British East Africa.
1907 RosenperaG, W. F. H., 57, Haverstock-hill, N.W. 3.
1868 Rornney, George Alexander James, Pembury, Tudor-road, Upper
Norwood, 5.E.
1888 ¢ Roruscuinp, The Right Honble. Lord, D.Sc., F.R.S., F.L.8., F.Z.S.,
(Councin, 1900), Zoological Museum, Tring.
1894 | Roruascuainp, The Honble. Nathaniel Charles, M.A., F.L.S., F.Z.S.,
(PRes., 1915-16; V.-Pres., 1914, 1917; CounciL, 1904, 1913-
17), Arwndel-house, Kensington Palace Gardens, W. 8.
1890 RournepaE, G. B., Tarn Lodge, Heads Nook, Carlisle.
1913. Rowopen, Alfred Oliver, 3, Archibald-road, Exeter.
1887 Rownanp-Brown, Henry, M.A., (V.-PRes., 1908, 1910; Src.,
1900-10 ; Counctn, 1914-16), Oxhey-grove, Harrow Weald.
1910 Rupes, Charles Henry.
1892 Russebn, 8. G. C., Monk’s Wood, Heatherside, Park-road, Woking.
PS Re RCaS
1905 Sr. Quintin, W. H., Seampton Hall, Rillington, York.
1906 Sampson, Colonel F. Winn, 115, Tannsfield-road, Sydenham.
(sm)
1910 Saunpers, H. A., Brookfield-house, Swanage.
1901 Scuaus, W., F.Z.S.,U.S. National Musewm, Washington, D.C., U.S.A.
1907 ScHMAssMANN, W., Beulah Lodge, London-rcad, Enfield, N.
1912. Scuunck, Charles A., Hwelme, Wallingford.
1911 Scorer, Alfred George, Hill Crest, Chilworth, Gavildford.
1909 Scorr, Hugh, M.A., F.L.S., Curator in Entomology, University
Museum of Zoology, Cambridge.
1911 Sxtovus, Cuthbert F., M.D., M.R.C.S., L.R.C.P.,- Sleaford, Penn
Hill, Parkstone, Dorset.
1911 + SenneErt, Noel Stanton, 24, de Vere-gardens, Kensington, W. 8.
1862 SsHarp, David, M.A., M.B., F.R.S., F.L.S., F.Z.S., (PREs., 1887-8 ;
V.-PREs., 1889, 1891-2, 1896, 1902-3; Sxc., 1867; Counct,
1893-5, 1902-4), Lawnside, Brockenhurst, Hants.
1902 SHarp, W. E., (Councrin, 1912-13), The Bungalow, Crowthorne,
Berks.
1915 Saw, Dr. A. Eland, c/o R. Kelly, Esq., Solicitor, 59, Swanston-
street, Melbourne, Victoria, Australia.
1886 SHaAw, George T. (Librarian of the Liverpool Free Public Library),
William Brown-street, Liverpool.
1905 Suetpon, W. George, (TREASURER, 1918— ), Youlgreave, South
Croydon.
1900 | SHEPHEARD-Watwyn, H. W., M.A., Dalwhinnie, Kenley, Surrey.
1887 + Stcu, Alfred, (CounctL, 1910-12), Corney House, Chiswick, W. 4.
1911 Srmes, James A., Mon Repos, Monkham’s-lune, Woodford-green, Essex,
1904 Simmonps, Hubert W., Sussex View, Cumberland-gardens, Tunbridge
Wells.
1913 Srrwet, Capt. F., Wooler, Northumberland.
1902 SrapeEn, Frederick William Lambart, Dept. of Agriculture, Central
Experimental Farm, Ottawa, Canada.
1902 Storer, Gerard Orby, F.ZS8., J.P., Badminton Club, Piccadilly, W.1.
1907 Sty, Harold Baker, 16, Sussex-square, Brighton,
1906 Smatuman, Raleigh 8., Eliot Lodge, Albemarle-road, Beckenham,
Kent.
1916 Smart, Capt. H. Douglas, R.A.M.C., Shelley, Huddersfield.
1915 Smira, Adam Charles, Horton, Mornington-road, Woodford Green.
1901 Smrru, Arthur, County Musewm, Lincoln.
1911 Smrrx, B. H., B.A., Frant Court, Frant, Tunbridge Wells.
1918 Smith, Patrick Aubrey Hugh, Sconner House, St. German's, Corn-
wall, and 28, Bruton-street, Berkcley-square, W.
1912 Smrrx, Roland T., 131, Queen’s-road, Wimbledon, S.W. 19.
1918 Smirx, 2nd Lieut. William Proctor, F.Z.S., Haddon House, Ashton-
on-Mersey.
1898 Sopp, Erasmus John Burgess, F.R.Met.8., 34, Ferndale-road, Hove.
1885 Sovurn, Richard, (Counctrt, 1890-1), 4, Mapesbury-court, Shoot-wp
Hill, Brondesbury, N.W. 2.
1916 Sowersy, Lieut. F. W., R.N.D., 94, Ainslie-street, Grimsby,
1908 SpryER, Edward R., Ridgehurst, Shenley, Herts.
1910
1898
1898
1910
1918
1910
1913
1915
1896
1900
1895
1908
1884
1894
1876
1911
1910
1908
1918
1918
1916
1911
TOU
1403
1914
1910
1901
1892
1907
1911
1897
1907
1914
1907
1906
1895
(e2xxvii 5)
Srantey, The Rev. Hubert George, Marshsield Vicarage, Cardiff.
Stares, C. L. B., M.R.C.S., L.R.C.P., The Limes, Swanley Junction,
Kent.
SrepBinG, Henry, Chasewood, Round Oak-road, Weybridge.
SrentToN, Rupert, Sf. Hdward’s, St. Mary Church, Torquay.
Srirr, Rev. Alfred T., Grantham, Victor Drive, Leigh-on-Sea.
StoneHAM, Hugh Frederick, Capt. Ist Batt. E. Surrey Regt.,
Stoneleigh, Reigate.
Srorey, Gilbert, Dept. of Agriculture, Cairo, Eqypt.
Srorr, Charles Ernest, Haton, Loudon road, Reigate.
STRICKLAND, T. A. Gerald, Southcott, Poulton, Fairford.
Srupp, E. A. C., P.O. Bow 906, Vancouver, British Columbia.
Stupp, E. F., M.A., B.C.L., Oxton, Exeter.
Swizrstra, Corn. J., Ist Assistant, Transvaal Museum, Pretoria.
SWINHOE, Colonel Charles, M.A., F.L.S., F.Z.S., (V.-Pres., 1894 ;
CounciL, 1891-3 ; 1902-4), 4, Gunterstone-road, West Kensing-
ton, W. 14.
SwinuHog, Ernest, 4, Gunterstone-roal, West Kensington, W. 14.
Swinton, A. H., Oak Villa, Brauishfield, Romsey, Hants.
Swynnerton, C. F. M., Gangunyana, Melsetter, S.-E. Rhodesia.
Tart, Robt., junr., Roseneath, Harborough-road, Ashton-on-Mersey.
Taeot, G., 138, Arthenden-voud, Brockley, S.E. 4.
Tapp, Mrs. Eleanor Eva, Loos, 88, Wickham Way, Beckenham, Kent.
Tapp, Capt. William Henry, F.R.A.S., F.R.G.S., Loos, 88, Wickham
Way, Beckenham, Kent.
TATCHELL, Leonard Spencer, 43, Spratt Hall-road, Wanstead, N.E.
Taurz, P. H., Cranleigh, Pinner, Middlesex.
Taytor, Frank H., Dalmally Station, vid Roma, Queensland.
Taytor, Thomas Harold, M.A., Yorkshire College, Leeds.
TEMPERLEY, Reginald, Sharpe House, Wiveliscombe, Somerset.
THEOBALD, Prof. F. V., M.A., Wye Court, Wye, Kent.
THOMPSON, Matthew Lawson, 40, Gosford-street, Middlesbrough.
THORNLEY, The Rev. A., M.A., F.L.S., “ Hughenden,” Coppice-road,
Nottingham.
TiLLyaRD, R. J., M.A., B.Sc., FLL.S., Linnean Macleay Fellow in
Zoology, Kuranda, Mownt Errington, Hornsby, New South Wales,
Topp, R. G., 54, Hornsey-lane, Highgate, N.
Tomuin, J. R. Je B., M.A., (Councin 1911-3), Lakefoot, Hamilton-
road, Reading.
TonGk, Alfred Ernest, (CounciL, 1915-17), Aincroft, Reigate, Surrey.
DE LA ToRRE BuENo, J. R., 25, Broad-street, New York, U.S.A.
TRAGARDH, Dr. Ivar, The University, Upsala, Sweden.
Tuxuocn, Col. B., The King’s Own Yorkshire Light Infantry, ¢/o
Messrs. Cox & Co., 16, Charing Cross, S.W.
TunaLgEy, Henry, Castleton, Searle-road, Farnham.
( =xxqvil)
1910 TurRatr1, Conte Emilio, 4, Piazza S. Alessandro, Milan, Italy.
1898 Turner, A. J.. M.D., The Manor War Hospital, Epsom, and
Wickham Terrace, Brisbane, Australia.
1893 TurNER, Henry Jerome, (Councrn, 1910-12), 98, Drakefell-road,
New Cross, 8.E. 14.
1906 Turner, Rowland E., (Counci1, 1909-10).
1915 Tyrer, Col. H. C., c/o Mrs. Tytler, Messrs. Grindlay & Co.,
Parliament-street, 8.W. 1.
1893 Uricu, Frederick William, C.M.Z.S., Port of Spain, Trinidad,
British West Indies.
1904 + Vauacuan, W., The Old Rectory, Beckington, Bath.
1914 Verrcn, Robert, Entomologist, c/o C.S.R. Co., Lantoka Mills,
Lantoka, Fiji Islands.
1909 Vipier, Leopold A., The Carmelite Stone House, Rye.
1911 Vurranis DE Satvaza, R., Vientiane, Laos, Indo-China.
1895 Wacuer, Sidney, F.R.C.S., Dane John, Canterbury.
1897 Warnwricnt, Colbran J., (CounciL, 1901, 1912-14), 139, Hamstead-
road, Handsworth, Birmingham.
1918 Watrorp, Lionel Julian, The Cavalry Club, Piccadilly, W.
1878 Waker, James J., M.A. R.N., F.L.S8., Secretary, 1905—;
(V.-Pres., 1916; Counctt, 1894; Suc. 1899), Aorangi, Lonsdale-
road, Summertown, Oaford.
1912 Watwace, Henry S., 6, Kayll-road Villas, Sunderiand.
1914 Watsu, Mrs. Maria Ernestina, Soekaboemi, Java, Dutch East Indies.
1866 + WaLsINGHAM, The Right Honble. Lord, I’.R.S., (PREs., 1889-90 ;
V.-PrEs., 1882, 1888, 1891-2, 1894-5; Councin, 1896), Briti:h
Museum (Natural History), Cromwell-road, S.W. 7.
1910 Warp, John J., Rusinwrbe House, Somerset-road, Coventry.
1908 Warren, Brisbane C. 8., Hotel Moy, Oberhofen, Lac de Thowne,
Switzerland.
1901+ WarerHousE, Gustavus A., B.Sc., F.C.S., Allonrie, Stanhope-road,
Killava, New South Wales, Australia.
1914. Warerston, Rev. James, B.D., B.Sc., 32, Blandford-road, Bedford
Park, W. 4.
1914 Warr, Morris N., St. John’s Hill, Wangonui, New Zealand.
1893 Wess, John Cooper, 89, Dulwich Village, 8.1. 21.
1876 | Western, E. Young, 27, Pembridge-square, Notting Hill Gate, W. 2.
1918 Weston, John Henry, 70, Ashford-road, Withington, Manchester.
1906 WHEELER, The Rev. George, M.A., F.Z.S., Secrerary, 1911— ;
(V.-Prues., 1914), 37, Gloucester-place, W. 1.
1910 Wutre, Major Edward Barton, M.R.C.S., Welsh Metropolitan War
Hospital, Whitchurch, Cardiff.
1918 Wutre, Ronald Senior, Suduganga Estate, Matale, Ceylon.
1913 + WuirLey, Percival N., Brantwood, Halifax,; and New College,
Oxford.
(Gy xacxe 9)
1913 + WuHirraKER, Oscar, Ormidale, Ashlands, Ashton-upon-Mersey.
1911
1
1906
1903
1896
1910
1911
1915
1915
1894
1905
1914
1918
1892
Wuirrrvauam, Rev. Canon W. G., Glaston Rectory, Uppingham.
WickuHam, Rev. Prebendary A. P., Hast Brent Vicarage, High-
bridge, Somerset.
Wickwar, Oswin 8., Woodford, Maitland Crescent, Colombo, Ceylon.
Wiaatns, Clare A., M.R.C.S., Entebbe, Uganda.
Winemay, A. E., Thatched House Club, St. James’-street, S.W. 1.
Wutcocks, Frank C., Entomologist to the Khedivial Agricultural
Society, Cairo, Egypt.
Witttrams, C. B., M.A., Port of Spain, Trinidad, and 20, Slatey-road,
Birkenhead.
WriusaMs, Harold Beck, 49, Marchimont-read, Wallington, Survey.
Winn, Albert F., Library of McGill Oniversity, Westmount,
Montreal, Canada.
Woutey-Dop, F. H., Millarville P. O., Alberta, N.W.T., Canada.
WooppribdGk, Francis Charles, Briar Close, Latehmore-avenue,
Gerrard’s Cross S.O., Bucks.
Wooprorpk, Francis Cardew, B.A., 2, Isis-slreet, Oxford.
WoopruFFE-Pracock, Rev. E. Adrian, F.LS., F.G.8S., Cadney
Vicarage, Brigg, Lincolnshire.
Youpatg, William Henry, F.R.M.S., 21, Belle [sle-street, Workington.
( Xxor- )
ADDITIONS OS DEE EEBRAR Y
Durinc THE YEAR 1918,
AnpREws (A. W.). Coleoptera collected in North-eastern Nevada by the
Walker-Newcomb expedition of the University of Michigan.
[Univ. Michigan, Occas. Papers, No. 48, 1917.]
Diptera collected on Whitefish Point, Chippewa County, Michigan.
[ Univ. Michigan, Occas. Papers, No. 53, 1918. ]
The University.
AnsorGE (E. C.). [See Lerroy (H. Maxwell).]
ArkwriGur (J. A.), Bacor (A.) and Duncan (F. M.). Preliminary notice
on the association of Rickettsia bodies in lice with trench
fever.
{ Reprinted from Brit. Medical Journ., Sept. 21, 1918.] .
Lister Institute.
Arrow (G.J.). [See Report on the Coleoptera of New Guinea. |
Back (EH. A.) and PemBerton (C. E.). The Melon-fly (Bactrocera cucur-
bitae, Coq.).
[U. 8. Dept. Agric., Bull. No. 643, 1918.] U.S. Dept. Agric.
Bacor (A.). The unreliability of sulphur for the destruction of lice in
clothing.
[ Brit. Medical Journ., Oct. 26, 1918. ]
Mosquitoes and the danger of Malaria in England.
[Essex Naturalist, Vol. XVIII, 1918.] The Author.
[See ArkwricutT (J. A.). |
Bairp (A. B.). Some Notes on the Natural Control of the Cherry-tree
ugly nest Tortricid, Archips cerastvorana, Fitch.
[Agric. Gazette of Canada, Vol. V, 1918.]
Canad, Dept. Agric.
BEMMELEN (J. F. van). The Wing-markings of drctzidae.
[Koningkl. Akad. Wet. Amsterdam, Vol. XX, 1917.]
The Author.
Bryer (H.). [See Lucinstrt (P.).]
Briair (K.G.). [See Report on the Coleoptera of New Guinea. |
Bore (J.). Les Motifs primitifs du dessin des ailes des Lépidoptéres et
leur origine phylétique.
[ Zool. Lab. der Rijksuniversitait Groningen, 1916. |
Dr. J. F. van Bemmelen.
Bravtey (J. C.). Contributions toward a Monograph of the Mutzllidae and
their allies of America north of Mexico. I. A Revision of
Ephuta, Say, a genus of Mutillidae equivalent to the species
group Scrupea ot Fox.
[Trans. Amer. Ent. Soc., Vol. XLII, 1916.]
—-— Contributions toward a Monograph of the MJZutzllidae and their
allies of America north of Mexico. II. A Revision of Timudlla,
Ashmead, a subgenus of JMJutilla equivalent to the species
group Hexagona of Fox.
[Trans. Amer. Ent. Soc., Vol. XLII, 1916.]
-———— Contributions toward a Monograph of the MJutillidae and their
allies of America north of Mexico. III. The J/util/idae of the
Eastern United States.
{Trans. Amer. Ent. Soc., Vol. XLII, 1916.]
(crx)
Bravery (J. C.). Contributions toward a Monograph of the J/utillidae and
their allies of America north of Mexico. IV. A Review of the
Myrmostdae,
[Trans. Amer. Ent. Soc., Vol. XLIII, 1917.]
———— Taxonomic notes on Agath7nae (Hymenoptera-Braconidae).
[Psyche, Vol. XXIII, 1916.] The Author.
Brooks (F. E.). Papers on Deciduous-fruit Insects. I. The Grape Curculio
(Crapontus tnaequalis, Say). II. The Grape Root-borer (Memy-
thius polist¢jormis, Harris).
[U. 8. Dept. Agric., Bull. No. 730, 1918.] U.S. Dept. Agric.
Broun (Major T.). Descriptions of new genera and species of Coleoptera.
Part V.
[New Zealand Institute, Bull. No. 1, June 1917.) The Author.
Burrer (A. G.). A Monograph of the Lepidoptera hitherto included in the
genus Llymnias.
[ Proc. Zool. Soc. Lond., 1871.]
——— On Two Collections of Lepidoptera sent by H. H. Johnston, Esq.,
C.B., from British Central Africa.
[Proc. Zool. Soc. Lond., 1893.]
On a Collection of Lepidoptera from British East Africa made by
Dr. J. W. Gregory between the months of March and August
1893.
[Proc. Zool. Soc. Lond., 1894. |
——— On Lepidoptera recently collected in British Hast Africa by Mr.
G. F. Scott Elliot.
[Proe. Zool. Soc. Lond., 1895.]
—-—— Ona small Collection of Butterflies made by Consul Alfred Sharpe
at Zomba, British Central Africa.
[Proc. Zool. Soc. Lond., 1895. | E. A, Elliott.
Catvert (P. P.). Progress in our knowledge of the Odonata from 1895 to
1912.
[Trans. Second Entom. Congress, 1912. |
——— An Entomologist in Costa Rica.
[Abstract of Address before Ent. Soc. Amer., Cleveland, Ohio,
Jan. 1, 1913. |
———— The Fossil Odonate Phenacolestes, with a Discussion of the Venation
of the legion Podayrion, Selys.
[Proc. Acad. Nat. Sci. Phil., 1913.]
——-— The Desirability of a Bibliographical Dictionary of Entomologists.
[Entom. News, Vol. XXV, 1914.]
——— The Completion of a Great Work (‘“ Biologia Centrali-Americana”).
(Notice of, with portraits of the Editors.)
[Entom. News, Vol. XX VII, 1916. ] G. C. Champion.
Cameron (A. E.). The Insect association of a local environmental complex
in the District of Holmes Chapel, Cheshire.
[Trans. Royal Soc. Edinburgh, Vol. LII, Part I, 1917. ]
The Soctety.
——— Life-history of the leaf-eating Crane-fly, Cylindrotoma splendens,
Doane.
[Ann. Ent. Soc. Amer., Vol. XI, 1918.]
Some Blood-sucking Flies of Saskatchewan.
[Agric. Gazette of Canada, Vol. V, 1918 ]
Canad. Dept. Agric.
——— and TreHErNE(R.C.). he Pear Thrips (Taeniothrips pyri, Dan.)
in British Columbia.
[Agric. Gazette of Canada, Vol. III, 1916.]
Canad. Dept. Agric.
(-cxxaan 3)
Cameron (A.E.) and TREHERNE. The Pear Thrips (7aentothrips inconsequens,
Uzel) and its control in British Columbia.
[Canad. Dept. Agric., Entom. Branch, Bull, No. 15, 1918.]
Canad. Dept. Agric.
CamMERON (M.). Synoptic Table of the British Species of 4Alewonota, Thoms.,
Atheta, Thoms., and Stpalia, Rey.
[ Trans. Ent. Soc. Lond., 1913. ]
———— Descriptions of new species of Staphylinidae from India.
[Trans. Ent. Soc. Lond., 1914. ]
On a new group of Staphylinid ve.
[Ent. Monthly Mag., 3rd Ser., Vol. III, 1917. ]
——-— Description of a new genus of Staphylinidae (Paraphytosus).
[Ent. Monthly Mag., 3rd Ser., Vol. III, 1917.]
———— Description of a new genus of Staphylinidae ( Paractochuris).
[Ent. Monthly Mag., 8rd Ser., Vol. ILI, 1917.]
——— — Description of a new species of Thinobius.
[Ent. Monthly Mag., 3rd Ser., Vol. III, 1917. ]
—— —— New Oriental Staphylinidae, I-III.
[Ent. Monthly Mag., 3rd Ser., Vol. IV, 1918.] The Author,
CARPENTER (G. H.). The Apterygola of the Seychelles.
[ Proc. Royal Irish Acad., Vol. XX XIII, Sect. B, No. 1, 1916.]
——— Zoological Results of the Abor Expedition, 1911-12. Collembola.
[ Records Indian Mus., Vol. VIII, 1917. ] The Author.
--——-— and Porttarp (F. J.S). The presence of lateral spiracles in the
larva of Hypoderma.
[ Proc. Royal Irish Acad., Vol. XXXIV, Sect. B, No. 4, 1918.]
The Author.
CarsneEk (Eubanks). [See Srauc (C. F.).].
Casey (T. L.). Memoirs on Coleoptera, Vol. VIII, 1918.
The Author.
CHAmpron (G. C.). New and little-known Saltatorial Dascillidae.
[Ent. Monthly Mag., 3rd Ser., Vol. IV, 1918. ]
—-— Note on the Curculionid, genus Sysciophthalmus, Heller, with a
description of a new species from Tierra del Fuego.
[Ent. Monthly Mag., 3rd Ser., Vol. IV, 1918. ]
—-—— The Coleoptera of the Falkland Islands.
[Ann. and Mag. Nat. Hist., Ser. 9, Vol. I, 1918.]
——--— Notes on various species of the genus Asty/us, Cast., with deserip-
tions of their sexual characters.
[Ann. and Mag. Nat. Hist., Ser. 9, Vol. II, 1918.]
——-— Notes on various species of the genus Cha/chas, Blanch.
[Ent. Monthly Mag., 8rd Ser., Vol. V, 1919. ] The Author.
Curistopu (H.). Neue Lepidoptera des Europaeischen Faunengebietes.
[ Horae Soc. Ent. Ross., Vol. IX, 1872. |
Zwei neue Schmetterlinge aus Persien.
[Horae Soc. Ent. Ross., Vol. XVII, 1882.]
———— Einige neue Lepidoptera aus Russisch-Armenien.
[Horae Soc. Ent. Ross., Vol. XVII, 1882. ]
—- Neue Lepidopteren aus dem Kaukasus. 4
[Romanoft’s Mémoires sur les Lépidoptéres, Vol. V, 1889. |
———~— Lepidoptera aus dem Achal-Tekke-Gebiete. :
[ Romanoff’s Mémoires sur les Lépidoptéres, Vol. V, 1889. |
——— Arctia turbans, eine neue Sibirische Art.
[Horae Soc. Ent. Ross., Vol. XX VI, 1892. ]
——— Lycaena cyane, Ev., und L. pylaon, Fd. W., etc. : ce
[Stett. ent. Zeit., 1893.] : E. A. Elliott.
Cement (G. E.). [See Moser (F. H.).]
( xxxan—)
Coan (B. R.). Recent experimental work on poisoning Cotton-boll weevils.
[U.S. Dept. Agric., Bull. No. 731, 1918. ]
» U, S. Dept. Agric.
CockerELt (T. D. A.). The Panurgine Bees of the genera Hesperapis,
Zacesta and Panurgomia,
[Psyche, Vol. XXIII, 1917.]
——— Insects in Burmese Amber.
[Ann, Ent. Soc. Amer., Vol. X, 1917.]
New Records of Natal Bees.
[Ann. Durban Mus., Vol. I, 1917.)
———— Neotropical Bees, principally collected by Professor Bruner in
Argentina.
[Trans. Amer. Ent. Soc., Vol. XLIV, 1918.]
—-—— The Megachilid Bees of the Philippine Islands.
[Philippine Journ. Sci,, Vol. XIII, 1918. |
The Mosquitoes of Colorado.
[Journ. Econ. Entom., Vol. IT, 1918.]
—-— The Bembecine Wasps (Hym.).
[Entom. News, Vol. XXIX, 1918.]
—-— Some Bees of the genus Panurginus (Hym.).
[Entom. News, Vol. XXIX, 1918. ] The Author.
Crippie (N.). Further observations upon the habits of the Western
Wheat-stem Sawfly in Manitoba and Saskatchewan.
[Agric. Gazette of Canada, Vol. V, 1917. ]
The Habits and Control of White Grubs in Manitoba (Lachnosterna,
spp. ).
[Agric. Gazette of Canada, Vol. V, 1918. ]
Canad. Dept. Agric.
Dr (M. N.). Second Report on the Experiments carried out at Pusa to
improve the Mulberry Silk Industry, compiled under the
direction of the Imperial Entomologist.
[Agric. Research Institute, Pusa, Bull. No. 74, 1917. ]
India Office.
Demacuy (E.). Notes d’Entomologie Scientifique. Premiére Note. La
Localisation du Sens de l’Odorat chez les Insectes.
[Amelie-les-Bains, Juin 1918. ] I. D, Godman.
Dewirz (H.). Afrikanische Schmetterlinge.
[ Mittheil. Miinch. Ent. Ver., 1879. ]
—- —— Westafrikanische Papilionen.
[Berl. ent. Zeitschr., Vol. XX VI, 1882. ]
West- und Centralafrikanische Tagschmetterlinge.
[Ent. Nachr., 1889.] E, A, Elliott.
[See Homeyer (A. V.).]
Distant (W. L.). Undescribed Rhopalocera from the Malay Peninsula.
(Ann. and Mag. Nat. Hist., Ser. 5, Vol. X, 1882.]
———— On some apparently undescribed Rhopalocera.
[Ann. and Mag. Nat. Hist., Ser. 5, Vol. X, 1882.]
E, A. Eltiott.
Doenin (P.). Hétérocéres nouveaux de l’Amerique du. Sud., Fase. XIV,
Nov. 1918. The Author.
DonistTHoRPE (H.). A List of Ants from Mesopotamia ; with a description
of a new species and a new variety.
[Ent. Record, Vol. XXX, 1918. ] The Author.
Dove (W. E.). Some Biological and Control studies of Gastrophilus
haemorrhotdalis and other Bots of horses,
[U. S. Dept. Agric., Bull. No. 597, 1918.]
U, S. Dept. Agric.
C
( -x=xmiv -.)
Druce (H.). Revonah: of some new species of Heterocera from ‘Tropical
Africa.
[Proc. Zool. Soc. Lond., 1886. ] EF, A. Elliott.
Duncan (F. M.). [See Anxwriacur (J. A.).]
Dyar (H. G.). Descriptions of New Lepidoptera from Mexico,
[Proc. U. S. Nat. Mus., Vol. LI, 1916.]
----—— Descriptions of New Lepidoptera from Mexico.
[Proc. U. S. Nat. Mus., Vol. LIV, 1918. ]
The Smithsonian Institution.
Epwarps (W. H.). On the History and the Pre paratory Stages of Fenestca
tarquinius, Pabr.
(Canad. Ent., Vol. XVIII, 1896.] E. A. Eltiott,
Ericuson (W. F.). Insecten: Schomburgk’s Reisen in Britisch-Guiana in
den Jahren, 1840-1844 (1848). BE. A, Elliott.
FLETcHE r(T. B.). Leerya purchasi in Ceylon: a warning to India.
{ Agric. Journ. India, Vol. XII, 1917. ] India Office.
Forwr (A.). Cadre synoptique actuel de la Faune universelle des fourmis.
[Bull. Soc, Vaud. Sci. Nat., Vol. LI, 1917.]
Etudes myrmécologique en 1917.
[Bull. Soc. Vaud. Sci. Nat., Vol. LI, 1917.] The Author.
Gauan (A. B.). Four new African parasitic Hymenoptera belonging to the
subfamily Microgasterinae.
(Proc. U. S. Nat. Mus., Vol. LIV, 1918.]
The Smithsonian Lustitutton.
Ganan (C. J.). [See Report on the Coleoptera of New Guinea. |
Ginson (A.). Cutworms and their control.
[Canad. Dept. Agric., Crop Protection Leaflet No. 3, 1918.]
——— Root Maggots and their control.
[Canad. Dept. Agric., Crop Protection Leaflet No. 4, 1918.]
———— Prevent White Grub i injury.
[Canad. Dept. Agric., Crop Protection Leaflet No. 5, 1918. ]
———— How to control Locusts and Grasshoppers.
(Canad. Dept. Agric., Crop Protection Leaflet No. 6, 1918. ]
————. The Pea-weevil (Br uchus pisorum, L.).
[Canad, Dept. Agric., Crop P rotection Leaflet No. 9, 1918. ]
——— The Alfalfa Looper (Autographa californica, Speyer).
{ Reprinted from the Agric, Gazette of Canada, Vol. V, 1918. |
Canad. Dept. Agric,
Git (J. B.). The Pecan leaf Case-bearer (Acrobatis nebulella, Riley).
[U. 8S. Dept. Agric., Bull. No. 571, 1917.]
UL S. Dept. Agric.
Gitterre (C. P.). [See Jonxs (T. H.).]
Gouau (L. H.). Notes on an Ephestia, an insect injurious to stored dates in
Khargeh Oasis.
[ Bull. Soc. Ent. d’Egypte (1917), 1918. ]
Ministry Agric., Cairo.
Green (EB. E.). A List of Coccidae affecting various genera of Plants.
[Ann. Applied Biology, Vol. IV, 1918. ] The Author.
Haas (Dr. Fr.). Consideraciones sobre los medios y fines de la investigacién
zoogeogrifica,
[Publicacions de la Junta de Ciencies Naturals de Barcelona, 1917. ]
La Junta de Ctencies.
Harcourt-Baru (W.). On the Vertical distribution of the Rhopalocera of
the Alps.
[Entom., Oct. 1895.]
———— Contributions to the geographical distribution of the Rhopalocera
of the Alps.
[Entom., 1896. ]
(rik)
Harcourt-Barn (W.). Among the spring butterflies in the Ardennes.
[Entom., Ang. 1896.)
A Seasonal dimorphism in British Butterflies,
[Entom., Aug. 1896.)
———— On the Vertical distribution and derivation of the Rhopalocera of
the Pyrenees.
[Entom., Oct. 1896.]
————— Should the formation and arrangement of a collection of insects
be made subservient to the elucidation of scientific problems ?
{Entom., Oct. 1896.)
———— On the preponderating influence of the organic over the physical
environment in determining the vertical distribution of the
Lepidoptera.
[ Entom., Dec, 1896. ] BE. A, Elliott.
Hawkers (Mrs. Onéra A, Merritt), Studies in inheritance in the hybrid
Philosamia (Attacus) rieint (Boisd.) ¢ x Philosamta cynthia
(Drury) ¢.
[ Journ. Genetics, Vol. VIT, 1918.] The Authoress.
Hesarp (M.). The Blattidae of North America north of the Mexican
boundary.
[Memoirs Amer. Ent. Soc., No. 2, 1917.]
, The American Ent. Soc.
Hewirson (W.C.). A Monograph of the Genus Vphthima; with descrip-
tions of two new genera of Diurnal Lepidoptera.
[Trans. Ent. Soc. Lond., 3rd Ser., Vol. II, 1865. 2. A. Elliott.
Hewirr (C, G.). The suppression of two insects affecting troops.
[Special Circular for Canadian Expeditionary Forces, Revised
Edition, 1917.]
Amendment to the regulations under the Destructive Inseet and
. Pest Act.
[Canada Dept, Agric., Suppl. No. 1 to Entom, Circular No, 10,1918. ]
Canad, Dept, Agric.
Hopgkiss (H. E.). [See Parrorr (P. J.).]
Hopson (‘T. V.). Parasitic Hymenoptera: Zchnewnontdae and Braconidae.
Type species in the Bignell Collection.
['Trans. Devonshire Assoc. Advance. Science, ete., 1917.)
The Author.
Horcann (W. J.). Contributions to a Knowledge of the Lepidoptera of
West Africa. I.
[‘Trans. Amer. Ent. Soc., Vol. XIII, 1886.]
—— — Contributions to a Knowledge of the Lepidoptera of West Africa.
Lig
‘Trans. Amer. Ent. Soc., 1888. ] E. A, Elliott.
Hotm@ren (Karin and Nils), Report on a Collection of Termites from
India.
[Agric. Research Institute, Pusa, Entom, Series, Vol. V, 1917.]
Tndta Office.
Homeryer (A. v.) and Dewrrz (H.). Drei neue westafrikanische Charaves.
[ Berl. ent. Zeitschr., Vol. XX VI, 1882.] EB. A, Eliott.
Horron (J. R.), Three-lined Fig-tree borer (Ptychodes trilineatus, L.).
[Journ. Agric. Research, Vol, XI, 1917. |
The Citrus Thrips (Sezrtothrips (Euthrips) evtri, Moul.),
[U.S. Dept. Agric.; Bull. No. 616, 1918.]
——— The Argentine Ant in relation to Citrus groves.
U.S. Dept. Agric., Bull. No. 647, 1918. U.S. Dept. Agric.
Hunter (W.D.). The Pink Bollworm (Pectinophora gossypiella, Saur J. ).
with special reference to steps taken by the Department of
Agyiculture to prevent its establishment in the United States.
[U. S. Dept. Agric., Bull. No. 723, 1918.] U.S. Dept. Agric,
( xxxvi )
Hurcuison (R. H.). Overwintering of the House-fly.
[Journ. Agric. Research, Vol. XIII, 1918. }
U.S. Dept. Agric.
Imus (A. D.). Observations on the Insect Parasites of some Coccidae.
II. On Chalcid Parasites of Zecandtum capreae.
[Quart. Journ, Microsp. Sci., Vol. LXIII, 1918.]
The Author.
Iset. (Dwight). Orchard injury by the Hickory tiger-moth (Halistdota
caryae, Harris).
LU. 8. Dept. Agric., Bull. No. 598, 1918.] U.S. Dept. Agric.
JANsE (A. J. T.). Two new South African species of Striphnopterygidae.
[ Ann. Transvaal Mus., Vol. V, Part 1, 1915.]
— — Contribution towards our Knowledge of the South African
Lymantridae.
{[Ann. Transvaal Mus., Vol. V, Part 1, 1915.]
South African Bagworms; notes on the Psychidae and on the
genera Gymnelema and Trichocossus, with descriptions of five
new species,
[Ann. Natal Mus., Vol. III, 1917.]
—— . — Some apparently undescribed //eterocera and five species hitherto
unrecorded from South Africa.
[Ann. Durban Museum, Vol. IT, 1918.] The Author.
JennrINGS (H.8.), Heredity; variation and the results of selection in the
uniparental reproduction of Deflugia corona.
[Genetics, Vol. I, 1916. ] The Author.
Jones (T. H.) and Giiterre (C. P.). Life-history of Pemphigus popult-
transversus.
[Journ. Agric. Research, Vol. XIV, 1918.] U.S. Dept. Agric.
Keys (J. H.). A List of the Maritime, Sub-maritime and Coast-frequenting
Coleoptera of South Devon and South Cornwall, with especial
reference to the Plymouth district.
[ Journ, Marine Biol. Assoc. Unit. Kingdom, Vol. XI, 1918.]
The Author.
Kurkarnt (G. 8.). Smuts of Jowar (Sorghum) in the Bombay Presidency.
[ Agric. Research Institute, Pusa, Bull. No. 78, 1918.]
India Office.
LANCASHIRE and Cheshire Entomological Society, Fortieth and Forty-first
Annual Reports and Proceedings. The Society.
Lea (A. M.). On Australian Coleoptera. Part I.
[Records of the S. Australian Mus., Vol. I, No. 1, 1918.]
The Museum.
Leacu (B. R.). Papers on Deciduous-fruit insects. III. Experiments in
the control of the root form of the Woolly Apple-aphis.
[U. 8. Dept. Agric., Bull. No. 7.0, 1918.] U.S. Dept. Agric.
Lerroy (H. Maxwell) and Ansorce (BE. C.). Report on an Inquiry into the
Silk Industry in India. Vols. I-III, 1916-17.
India Office.
Lronanrpi (Gustao). Necrologio, by Filippo Silvestri.
[Boll. Lab. Zool, R. Scuola d’Agric. Portici, Vol. XI, 1918.]
F. Silvestri.
Lueinpitt (P.) and Bryer (H.). Contribution to the Knowledge of
Toxoptera grantnum in the South. :
(Journ. Agric. Research, Vol. XIV,1918.] U.S. Dept. Agric.
McAurine (W. 8.). A Collection of Lepidoptera from Whitefish Point,
Michigan :
[Univ. Michigan, Oecas. Papers, No, 54, 1918.] The University.
MeInpoo (N. E.). Effects of Nicotine as an insecticide.
[Journ. Agric, Research, Vol. VU, 1916.] U.S, Dept. Agric.
(© xxxvib »)
Macnamara (C.). The Original Paper-makers (Vespa maculata).
{Ottawa Naturalist, Vol. XXXII, No. 3,1918.] HH. Donisthorpe.
Marsnavu (G. A. K.). [See Report on the Coleoptera of New Guinea. ]
Mrapr-Watpo (G.). [See Report on the Hymenoptera of New Guinea. |
Me tvitt (J. Cosmo). Description of a new Butterfly of the genus Calinaya
from Siam. :
[Trans. Ent. Soc. Lond., 1893. ] E. A. Elliott.
Meyrick (K.). Exotic Microlepidoptera.
[Vol. Il, Pts. 2-7, Oct. 1917-Oct. 1918. ] The Author.
MIciikeEN (F. B.). Mysius ertcae, the False Chinch Bug.
[Journ. Agric. Research, Vol. XIII, 1918.]
U.S. Dept. Agric.
Minor (C.8.). Obituary notice and portrait of, by Dr. Henry H. Donaldson.
[Proc. Bost. Soc. Nat. Hist., Vol. XX XV, 1915.]
The Soctety.
Misra (C. 8.). The Present Condition of Lac Cultivation on the Plains of
India.
[ Agric. Journ. of India, Vol. XIII, Part III, 1918.]
India Office.
Moore (F.). A Monograph of Limnaina and Euploetna, two groups of
Diurnal Lepidoptera belonging to the sub-family Kuploeinae ;
with Descriptions of new Genera and Species.
[ Proc. Zool. Soc. Lond., 1883. ] E. A, Eltiott.
Mortry (C.). [See Victoria History of the Counties of England: Suffolk.]
——-—— [See Report on the Hymenoptera of New Guinea. |
Mosner (F. H.) and Crrmenr (G. E.). Some timely suggestions for the
owners of woodlots in New England (contains remarks on food
of Gipsy-moth larvae). Pamphlet dated 1917.
U.S. Dept. Agric.
Mosquito Danger, The. Poster issued by the British Museum (Natural
History), South Kensington, London, 8.W.7 (not dated).
Trustees, British Museum.
Muersrseck (C.F. W.). Two important introduced parasites of the Brown-
tail Moth.
[Journ. Agric. Research, Vol. XIV,1918.] U.S. Dept. Agric.
Neave (8. A.). Ona large Collection of Rhopalocera from the shores of the
Victoria Nyanza.
LNov. Zool., Vol. XI, 1904.] The Author,
Newcomer (EH. J.). Some Stone-flies injurious to vegetation.
[Journ. Agric. Research, Vol, XIII, 1918.]
U. S. Dept. Agric.
Newsteap (R.). Polypneustic Lobes in the Larvae of T'setse-flies (Glossina)
and Forest-flies (//ippoboscidae).
[Ann. Tropical Medicine and Parasitology, Vol. XII, 1918.]
The Author.
NichvILLE (L. de). Note on Papilio polydecta of Cramer.
[Trans. Ent. Soc. Lond., 1884.] E. A. Elliott.
OserTuiiR (C.). Etudes de Lépidoptérologie Comparée. Fasc. XV, XVI.
1918. The Author.
Ormiston (W.). Notes on Ceylon Butterflies. (Part I: Species 1-146.)
[Spolia Zeylanica, 1918. ] The Author
Parrotr (P. J.) and Hopexiss (H. E.). Miscellaneous notes on injurioue
insects.
[New York Agric. Exper. Station, Bull. No. 423, Aug, 1916.]
N.Y. Agric. Exper. Station.
Pearson (R.8.). Note on Kokan or Lampatia Timber, Duabanga sonnera-
tioides, Ham.
[Forest Research Institute, Dehra Dun, Forest Bull. No. 36, 1917.)
®
(( xxxviil ~-)
Prarson (R.S.). Note on the Contraction and Warping which takes place
in Pinus longifolia timber while seasoning.
[Forest Research Institute, Dehra Dun, Forest Bull. No. 37, 1917.]
———— The Indian Forest Records. A Further Note on the Antiseptic
Treatment of Timber, recording results obtained from past
experiments.
[Indian Forest Records, Vol. VI, 1918.] India Office.
[See Indian Forest Records. ]
PEMBERTON (C. E.). [See Back (E. A.).]
and Wittarp (H. F.). Interrelations of Fruit-fly parasites in
Hawaii.
(Journ. Agric. Research, Vol. XII, 1918.]
Fruit-fly parasitism in Hawaii during 1916,
[Journ. Agric. Research, Vol. XII, 1918.]
- Work and parasitism of the Mediterranean Fruit-fly in
Hawaii during 1917.
[Journ. Agric. Research, Vol. XIV, 1918.] U.S. Dept. Agric.
PrickARD-CAMBRIDGE (Octavius). Memoir of, by his son Arthur Wallace
Pickard-Cambridge. Oxford, 1918.
A. W. Pickard-Cambridge.
Picrer (A.). Résistance des Lépidoptéres 4 la compression, 4 l’asphyxie et
au froid.
[Compt. Rendu Soc. Physique et d’Hist. Nat. de Genéve, Vol.
XXXIV, 1917.]
—— Sur Porigine de quelques races geographiques de Lépidoptéres.
[Compt. Rendu Soc. Physique et d’Hist. Nat. de Genéve, Vol.
XXXIV, 1917.)
——-— Intervention de l’élévation de la température pour provoquer
Véclosion des Papillons.
[Compt. Rendu Soe. Physique et d’Hist, Nat. de Genéve, Vol.
XXXV, 1918.]
—-—— Sur lorigine du dimorphisme sexual de coloration chez les
Leépidopteres.
[Compt. Rendu Soc. Physique et d’Hist. Nat. de Genéve, Vol.
XXXYV, 1918.] By Eachange.
Pierce (W. D.). The Comparative morphology of the Order Strepsiptera
together with records and descriptions of Insects.
[Proc. U. S. Nat. Mus., Vol. LIV, 1918.]
The Smithsonian Institution.
PottarD (F. J.§.). [See Carpenter (G. H.).]
Povutron (E. B.). On Dr. C. A. Wiggins’ Researches on Mimicry in the
Forest Butterflies of Uganda (1909).
[ler Congrés Intern. d’Entomologie, Bruxelles, 1910.]
—-—— Mimicry, Mutation and Mendelism. :
[ Reprinted from Bedrock, April 1913.] E. A. Elliott.
Report on the occurrence of insect and fungus pests on plants in England
and Wales in the year 1917.
[Board Agric. and Fisheries, Miscell. Publ. No. 21, 1918.]
Board Agric., London.
Report of the Council of the Royal Agricultural Society of England, 1917.
The Soctety.
Report of the Council of the Royal Agricultural Society of England, Dec.
11th, 1918. The Society.
Report of the Progress of Agriculture in India for 1916-17. 1918. —
India Office.
Report, Nineteenth, of the Michigan of Science, 1917. The Academy.
-
(- xxxix ")
Report of the Entomologist, U. 8. Dept. Agriculture, Sept. 1918.
[Papers by A. L. Quaintance, W. R. Walton, F. H. Chittenden.
W. D. Hunter, A. D. Hopkins, C. L, Marlatt, J. A. Hyslop,
H. F. Phillips. U.S. Dept. Agric.
Report, Forty-eighth Annual, of the Entomological Society of Ontario, 1917.
Issued 1918. The Society.
Report of the Agricultural Research Institute, Pusa (including the Report
of the Imperial Cotton Specialist), 1916-17. Lndta Office.
Report, Scientific, of the Agricultural Research Institute, Pusa (including °
the Report of the Imperial Cotton Specialist), 1917-18.
India Office.
Report of the Imperial Entomologist, 1917-18.
[Scient. Reports Agric. Res. Inst., Pusa, 1917-18. ]
India Office.
Report of the National Trust for places of historic interest or natural beauty,
1917-18. London, 1918. The Trust.
Report on the Progress and Condition of the United States National Museum
for the year ending June 30,1917. Issued 1918.
The Smithsonian Institution.
Report on the Hymenoptera collected by the British Ornithologists’ Unicn
Expedition and the Wollaston Expedition in New Guinea. By
Rk. E. Turner, G. Meade-Waldo, and C. Morley.
[Issued in Vol. II of the Reports by the ‘‘ New Guinea Committee,”
dated 1916. ] E. A, Elliott.
Reports on the Coleoptera collected by the British Ornithologists’ Union
Expedition and the Wollaston Expedition in Dutch New Guinea.
Parts I-IV. PartI. By G. J. Arrow. Part II. ByG. A. K.
Marshall. Part III. By C. J. Gauan. Part IV. By K. G.
Blair.
[Parts I, II, and IV, published in the Trans. Zool. Soc. Lond, Vol.
XX, Oct. 1915; Part III, and “ Addenda et Corrigenda ” to
Parts IL and ITI, in Vol. II of the Reports ‘*‘ New Guinea Com-
mittee,” dated 1916. C. J. Gahan.
Rosrnson (Elizabeth). Descriptions and Records of Philippine Coccidae.
[Philippine Journ. Sci., Vol. XIIT, 1918. ]
Philippine Bureau Sctence.
Roaers(J.8.). A collection of Tipulidae from Schoolcraft County, Michigan.
[Univ. Michigan, Occas. Papers No. 55, 1918.]
The University.
Rouwer (8S. A.). Descriptions and notes on some Ichneumon flies from
Java.
[Proc. U. S. Nat. Mus., Vol. LIV, 1918.]
The Smithsonian Institution.
Ross (W. A.). The Cyclamen Mite ( Tarsonemus).
(Agric. Gazette of Canada, Vol. IV, 1917. ]
—— — Some Ladybird beetles destructive to Plant lice.
(Agric. Gazette of Canada, Vol. V, 1918. |
——-— Aphids or Plant lice.
[Canad, Dept. Agric., Crop Protection Leaflet, No. 8, 1918. ]
Canad, Dept. Agric.
Sanpers (G. F.). Arsenate of lime (Calevum arsenate).
[Canad. Dept. Agric., Crop Protection Leaflet, No. 10, 1918.]
Canad. Dept. Agrie.
—-— [See Swaine (J. M.).]
Sanrorp (H.L.). [See Sasscer (EH. R.).]
Sasscer (E. R.) and Sanrorp (H. L.). Effect of hydrocyanic-acid gas under
vacuum conditions on subterranean larvae. ;
‘ [Journ. Agric. Research, Vol. XV, 1918. ] U.S. Dept. Agrie.
( xl )
Scuaus (W.). On new species of Heterocera from Tropical America.
[Proe. Zool, Soc. Lond., 1894.
On Walker’s American Types of Lepidoptera in the Oxford Uni-
versity Museum.
[ Proc. Zool. Soc. Lond., 1896. ]
——— New species of Heterocera.
[Journ. New York Ent. Soc., June and Sept. 1896. ]
———-- New species of Heterocera from Tropical America.
[Journ. New York Ent. Soc., Dec. 1896. ] E. A. Elliott.
SELKREUG (EH. R.). [See Woop (W. B.).]
Sen (8. K.). Beginnings in insect physiology and their economic importance.
[ Agric. Journ. of India, Vol. XIII, 1918. ] India Office.
SHELForD (R. W.C.). A Naturalist in Borneo. London, 1916.
FE. B. Poulton.
SitveEstrI (F.). Contribuzione alla conoscenza del yenere Centrobia, Forster
(Hymenoptera: Chalcididae).
[Boll. Lab. Zool. R. Scuola d’Agric. Portici, Vol. XII, 1918. ]
——-—- Descrizione e notizie biologiche di aleuni Zmenotter? Calcidid? paras-
siti di nova di Cicale.
[Boll. Lab. Zool. R. Scuola d’Agric. Portici, Vol. XII, 1918.]
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[ Boll. Lab. Zool. R. Scuola d’ Agric. Portici, Vol. XII, 1918.]
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[ Boll. Lab. Zool. R. Scuola d’Agric. Portici, Vol. XIT, 1918. ]
The Author.
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tenella) nonvirulent to Curly-top.
[Journ. Agric. Research, Vol. XIV, No. 9, 1918.]
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[Canad, Dept. Agric., Entom. Branch, Circular No. 11, 1918.]
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SwInHoE (C.). A List of the Lepidoptera of the Khasia Hills. Part IT.
(Trans. Ent. Soc. Lond., 1894. ]
A List of the Lepidoptera of the Khasia Hills. Part III.
[ Trans. Ent. Soc. Lond., 1895. ] EB. A. Elliott.
Toruity (J. D.). The Predaceous Mite, //emisarcoptes malus, Shimer, and
its relation to the natural control of the Oyster-shell scale,
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[Agric. Gazette of Canada, Vol. V,1918.] Canad. Dept. Agric.
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[ Agric. Gazette of Canada, Vol. V,1918.] Canad. Dept. Aqric.
—— [See Cameron (A. E.).]
Turati (Conte Emilio). Variabilitaé del Parnasstus apollo pumilus, Stich., e
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[Atti Soc. Ital. Sci. Nat., Vol. LVII, 1918. ] The Author.
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Urpauns (T.D.). Tetrastichus bruchophagi, a recently described parasite of
Bruchophagus funebris.
(Journ. Agric. Research, Vol. VIII, 1917.] U.S. Dept. Agric,
(alt)
VICTORIA Hisrory of the Counties of England. Insects; Suffolk, by C.
Morley, 1902. Warwick, by C. J. Wainwright, R. C. Bradley,
A. H. Martineau, H. Willoughby Ellis, 1904. EA. Elliott.
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Watson (J.). On Parnassius phoebus (Fab.) = delius (Esp.), and P, smin-
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[Entom., 1894. ]
-——— On Three Hybrid Silk-moths hybridised and bred in North America.
[Entom., June 1893. ]
———\ Breeding Exotic Bombyces in 1898.
[Entom., Oct. 1893. ]
———— The Sense organs of Insects: a Speculation.
[Entom., 1895. | E. A. Elliott.
Watson (J. H.). Stray Notes on Parnasstus.
[Reprinted from Fourteenth Ann. Report Manchester Ent. Soc. 1915. ]
The Author.
Watts (G. F.). Sacbrood.
[U. 8. Dept. Agric., Bull. No. 431, Professional Paper, 1917. ]
UL S., Dept. Agric.
Wittarp (H. F.). [See PEMBERTON (C. E.).]
WituiaAMson (E. B.). Twointeresting new Colombian Gomphines (Odonata).
[Univ. Michigan, Occas. Papers, No, 52, 1918. ]
The University.
Woop (W. B.) and Serkreae (E. R.). Further Notes on Laspeyresia molesta.
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Yorurrs (W. W.). Some reasons for spraying to control insect and mite
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* Ln
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be
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TRANSACTIONS
ENTOMOLOGICAL Se
OF AK aks "Er
LONDON
For THE YEAR 1918,
eae
Ser ak
I. Coleoptera of the families Ostomidae, Monotomidae,
Colydiidae and Notiophygidae from the Seychelles
and Aldabra Islands. By the late ANTOINE GROUVELLE.
Communicated by Hueu Scott, M.A., F.L.S.
Pranes. li:
[Read December 5th, 1917.]
[THE material here reported on forms part of the entomologi-
cal collections made by the Percy Sladen Trust Expedition
of 1905 and 1908-9 in the Seychelles and other islands of
the Western Indian Ocean. The late author of the paper
had already dealt with certain other families of Clavicorn
Coleoptera obtained in those islands, in the special series
of the Linnean Society’s Transactions set apart for results
of that Expedition : see Trans. Linn. Soc. London, ser. 2,
Zool., vol. xvi, pp. 93-116 (1913), and vol. xvu, pp.
141-159 (1914). The manuscript of the paper printed
below was received from him in Oct. 1915, but circumstances
hitherto have prevented its publication, while the author’s
death on June 9, 1917, renders it a posthumous work.
The correction of the proofs has presented some difficulty,
therefore indulgence is asked, especially from French
readers, towards any textual and grammatical errors.
I am responsible for the notes on localities, and on
reduction of wings and eyes in certain species (pp. 24, 41, 45).
As in most groups, the greater part of the coliection was
obtained in the endemic forests in the mountains of the
Seychelles proper. The spaces between the leaf-bases of
srowing endemic palms and Pandanus proved a good
hunting-ground for these insects, the material of six of the
TRANS. ENT. SOC. LOND. 1918.—PARTS I, 1. (DEC.) B
2
M. Antoine Grouvelle on
new forms described below being derived partly or wholly
from this source.
The first set of specimens, with types of all new genera
and species here described, is in the British Museum.
A
second series is in the Cambridge University Museum.—
Huenr Scorr. |
Ce mémoire énumére 34 espéces, dont 26 nouvelles,
appartenant & 22 genres différents, dont 4 nouveaux. Ce
simple énoncé fait ressoriir importance des découvertes
faites par la Percy Sladen Trust Expedition.
“a =a
fe} C43
D of oo Ace
38 & Ve 9
= a | B88
a pa to
ad oO Poss
5 be Fae a ace yes
Lo Sis
» [o} eH
wn a 0 AY
oO cs
OSTOMIDAL.
» Alindria costulata
Lophoeateres pusillus
MONOTOMIDAE.
Monotoma madagascariensis
Shoguna polita . .
COLYDIIDAL.
Sarothrias eximius
Pycnomerus confertus
Ditoma cavicollis .
Xuthia sicana .
Cicones seotti .
compactus
Colobicones singzularis
Diplotoma ecapito .
Neotrichus gardineri .
= parallelocollis
Lascotonus scotti .
Paralyreus scotti .
Tyrtaeus singularis
Mecedanum sp. .
Bothrideres fryer .
Cerylon vitidum
longius é
perparvulum .
tantillum .
gardineri .
liliputanum
curtulum .
Axiocerylon cavicolle .
Thyroderus seulpticollis
Mychocerus alluaudi .
NOTIOPHYGIDAE.
Aphanocephalus insularis
binotatus
— acuminatus
4-plagiatus .
subdepressus
Groupes Aldabra
(inel, Aldabra
Astove, Assump-
ion et Cosmoledo).
it
DISTRIBUTION GHOGRAPHIQUE DES ESPECES CATALOGUBES DANS CE MEMOIRE
|
Provenance
des espéces
déja deécrites.
Cosmopolite.
Madagascar.
ChristmasIsland.
Madagascar.
{ Archipel Malais
\ Inde.
Seychelles,
Seychelles.
* Also Mauritius (see p. 50).
Coleoptera of the families Ostomidae, Monotomidae, elec. 3
OSTOMIDAE,
Cette famille est représentée par deux espéces dans les
collections récoltées par la Percy Sladen Trust Expedition.
La premiére, Alindria costulata, appartenant a la sous-
famille des Temnochilinae, est nouvelle et semble spéciale
& la faune de ces iles. Le genre Alindria se rencontre
dans toute Afrique tropicale et sub-tropicale, ainsi que
dans |’Asie méridionale en remontant jusquaux frontiéres
de la Chine, il est représenté & Madagascar et dans l’Inde
par des formes locales, il n’a pas encore été retrouvé aux
Iles Maurice et de la Réunion.
La deuxiéme, Lophocateres pusillus (Klug), appartient
a la sous-famille des Ostominae ; elle est cosmopolite.
TEMNOCHILIN AE.
AutnprRiA, Erichson, 1844, in Germ., Zeitschr., V, p. 451.
1. Alindria costulata, n. sp.
Parallela, fere sexies longior quam latior, convexa, in disco subde-
pressa, elytris subcostata, glabra, nitida, viridi-aenea; elytrorum
costis aeneis, antennis pedibusque rufo-piceis, illis ad apicem cyaneo-
aeneis. Antennae pro genere sat elongatae; 3° articulo quadrato,
9° quam 8° minus duplo latiore, clava apice stricte pubescenti.
Caput disco subdepressum, tenuissime alutaceum, sat dense puncta-
tum. Prothorax paulo longior quam latior, vix perspicue alutaceus,
subdense punctatus; punctis in disco elongatis; margine antico ad
extremitates marginato; angulis anticis vix productis. Elytra
basi haud marginata, in longitudinem costulata, punctata; punctis
elongatis praecipue in costularum intervallis densatis et sublineato-
dispositis, ad latera minoribus, subelongatis, fere confusis. Long.
75 mill.
Paralléle, presque six fois plus long que large, convexe, sub-déprimé
sur le disque, glabre, brillant, marqué sur les élytres de cdtes peu
accentuées, bronzé-verdatre, cdtes des élytres simplement bronzées ;
antennes et pattes plus ou moins roux de poix; les premiéres bleu-
métallique vers l’extrémité; dessous du corps noir. Antennes assez
allongées pour le genre: 1° article épais, un peu plus long que large,
2™¢ environ deux fois plus large que long, 3™¢ carré, 4™¢ 4 8™ s’élargis-
sant progressivement, subégaux, le 4™° un peu plus court que le
om, 8™° presque deux fois plus large que 3™*, 9™¢ et 10™* transvers-
aux, subégaux, moins de deux fois plus larges que 8™*, 11™° un peu
4 M. Antoine Grouvelle on
plus long que 10™°, bordé 4 lextrémité par une trés étroite marge
pubescente. Téte un peu plus longue que large, subdéprimée sur
le front, couverte d’une ponctuation un peu allongée, assez serrée ;
yeux légérement éloignés de la base de l’antenne. Prothorax un
peu plus long que large, couvert d’une ponctuation assez dense, trés
nettement allongée sur le disque; bord antérieur 4 peine cilié sur
les extrémités, trés briévement rebordé de chaque cdté; angles
antérieurs 4 peine saillants en avant; cOtés subparalléles, finement
rebordés ; angles postérieurs obtus; base arquée, finement rebordée.
Ecusson petit, suborbiculaire. Elytres environ quatre fois plus
long que large ensemble, arrondis ensemble au sommet, non rebordés
& la base, marqués de points linéaires, plus ou moins serrés, et plus
ou moins disposés en lignes sur les intervalles des cOtes, beaucoup
plus rares sur celles-ci, fins, peu allongés, espacés et confus sur les
marges latérales; celles-ci finement rebordées. Hanches antérieures
rougeatres : saillies du premier segment de Vabdomen entre les
hanches postérieures ne s’engageant pas dans une échancrure du
métasternum.
1 exemplaire.
Loc. ALDABRA. Ile Esprit, xii. 1908 (Fryer).
OSTOMIN AE.
LopnocaTErEs, Olliff, 1883, Trans, Ent. Soc. Lond., p. 180;
1883, Cistula Ent. in, p. 58.
2. Lophocateres pusillus, Klug.
Peltis pusillus, Klug, 1832, Abh. Akad. Wiss. Berlin, p. 159.
Peltis africanus, Motschulsky, 1853, Bull. Soc. Nat. Moscou,
XXXVI, ui, p. 508.
Peltis yvani, Allibert, 1847, Rev. Zool., p. 12.
Ostoma yvani, Reitter, 1876, Verh. Nat. Ver. Briinn, XIV,
p. 63.
Kspéce cosmopolite. 1 exemplaire.
Loc, SEYCHELLES. Silhouette, vii. 1908.
MONOTOMIDAE.
Deux espéces appartenant a deux genres différents
figurent dans les collections de la Perey Sladen Trust
Expedition. Le genre Monotoma se rencontre dans toutes
les parties du monde, le genre Shoguna est représenté
jusqu’a ce point par un petit “nombre d’espéces appartenant
Coleoptera of the families Ostomidae, Monotomidae, etc. 5
i la faune de l’ancien monde et de POcéanie. Les espéces
du méme groupe qui se rencontrent dans |’Amérique Cen-
trale sont cataloguées dans un genre Thione, Sharp (1899,
Biol. Centr.-Am., Col. II, 1, p. 544), trés voisin de Shoguna,
La position systématique ‘de ces deux genres dans les
Monotomidae ne me semble pas nettement établie.
Monoroma, Herbst, 1793, Kaf., V, p. 22.
3. Monotoma madagascariensis, Grouvelle.
Monotoma madagascariensis, Grouvelle, 1906, Ann. Soe.
Ent. France, LX XV, p. 126.
Le type de l’espéce provient de Madagascar, Vexemplaire
des Seychelles est presqu’ identique a ce type; ses calus
huméraux sont un peu moins accentués.
Loc. SEYCHELLES. Mahé: “ One specimen, from country
above Port Glaud, between 500 and 1000 feet, 5. xi. 1908.”
SHocuna, Lewis, 1884, Ann. Mag. Nat. Hist., Ser. 6, IV,
p. 274; Ser. 6, XIII, 1894, p. 485.
Holocephala, Fairm., 1886, Ann. Soc. Ent. France, 6 Ser.,
VI, p. 32.
Pachycephala, Fairm., 1883, Ann. Soc. Ent. Belg., X XVII,
p. 4.
4. Shoguna polita, Arrow.
Shoguna polita, Arrow, 1900, Monog. Christmas Island, p. 92.
Le type de l’espéce provient de Christmas Island. Sho-
guna polita, Arrow, différe de S. chlorotica, Fairm., par ses
élytres & peine striés en dehors de la région suturale; il
est beaucoup plus rapproché de S. ter mitifor mis, Fairm.,
de Samoa.
Loc. SEYCHELLES. Mahé: “A single specimen caught by
daylight on the wing near the house at Cascade Estate,
800 feet, 1909, in the vicinity of much imported vegetation.’
COLYDITDAE.
Les Colydiidae des Seychelles et surtout les Cerylini sont
rélativement nombreux; 25 espéces ont été récoltées.
Toutes sauf trois sont nouvelles, 5 ont nécessité des genres
nouveaux.
6 M. Antoine Grouvelle on
-Sarothrias-—Nouveau genre établi pour un insecte de
forme et de structure tout-a-fait spéciales, appartient a la
tribu des Apistini. I] droit étre localisé dans la région
des Seychelles.
Pycnomerus.—Une seule espéce, déji connue de Madagas-
car, elle se rapporte au sous-genre Penthelispa.
Ditoma.—Une seule espéce nouvelle qui comme aspect
et structure générale ne s’écarte en rien du groupe cosmo-
polite des Ditoma.
Xuthia.—Une seule espéce, X. sicana, Pasc., répandue
dans tout l’Archipel malais, les Indes, ete.
Cicones—Deux espéces nouvelles. La premiére, C.
scolti, rentre bien dans le type classique du genre Cicones :
la seconde, C. compactus, s écarte de ce type et rentre dans
un ensemble de formes qui toutes répondent aux caractéris-
tiques du genre mais montrent Popportunité de subdivisions
établies sur l'étude de matériaux importants. Malheureuse-
ment ces formes voisines des Cicones proprement dit sont
en général représentées par des exemplaires uniques, qui
ne permettent pas toutes les études de détail qui seraient
nécessaires,
Colobicones.—Nouveau genre établi pour une espeéce
nouvelle, venant se placer entre les Ditoma, les Cicones et
les Colobicus.
Diplotoma.—Ce genre, établ par Erichson pour deux
Colydiidae de Madagascar, décrits postérieurement par
Reitter, semble pour Je moment localisé dans la région de
Madagascar, des Mascareignes et des Seychelles; mais il
serait prématuré de formuler une conclusion absolue a cet
égard. L’espéce des Seychelles est nouvelle et ne présente
rien de bien saillant par rapport aux espéces connues.
Neotrichus.—Deux especes nouvelles. Ce genre est
représenté dans presque toutes les faunes tropicales et
sub-tropicales.
Lascotonus.—Une espéce nouvelle. Ce genre comprend
déja une espéce de l’Afrique orientale et deux des Indes
orientales.
Paralyreus.— Genre nouveau établi pour un petit Colydien
qui rappelle les insectes subhypogées de la faune paléarc-
tique.
Tyrlaeus. Ce genre a été établi par Champion pour deux
espéces de l’ Amérique centrale ; il semble avoir des représen-
tants dans toute la zone tropicale; je connais en effet trois
autres espéces qui doivent lui étre rapportés : lune provient
Coleoptera of the families Ostomidae, Monotomidae, etc. 7
de la Guadeloupe, les deux autres de Sumatra. Le genre
Tyrtaeus me semble placé avec raison parmi les Colydiidae,
lécartement modéré, de ses hanches postérieures et |’ ensem-
ble de ses autres caractéres le rangerait entre les Ditomini
et les Coxelini; provisoirement je le rapporterai 4 cette
dernier tribu. Les Tyrtaeus vivent probablement de
matiéres cryptogamiques.
[The late author left no remarks on these
two genera in his MS. According to an
eee earlier statement by him (Ann. Soc. Ent.
: ", France, LXXV, 1906, p. 107), several
Bothrideres. | -
species of Mecedanum are known, from
Madagascar and W. Africa. Bothrideres is
represented in all parts of the world. |
Cerylon—Les Cerylon sont nombreux aux Seychelles.
Les collections de la Perey Sladen Trust Expedition renfer-
ment sept espéces dont six nouvelles: quelques unes sont
représentées par un nombre considérable d’exemplaires.
Le genre Cerylon se retrouve dans toutes les régions, ses
espéces sont trés nombreuses.
Axiocerylon.—Genre nouveau établi pour un des Cerylini
trés remarquable par sa forme et sa sculpture. Ce genre a
d’autre représentants dans [Afrique occidentale.
Thyroderus.—Genre établi sur une espéce du Japon et de
Ceylan. La forme nouvelle des Seychelles est particuliére-
ment intéressante; sa capture, comme du reste celle des
minuscules Cerylon rapportés par la Percy Sladen Expedi-
tion, fait prévoir de nombreuses découvertes dans le monde
des petits Colydiens du groupe des Cerylini.
Mychocerus.—Ce genre établi par Erichson pour un insecte
inédit de Cuba, M. ferrugineus, puis adopté par Zimmerman
pour le M. depressus, Lee., semble répandue dans toutes
les faunes tropicales et subtropicales.
COLYDIINAEH. APISTINI.
SAROTHRIAS, nov. gen.
Antennae 1l-articulatae, supra oculos insertae et ab his remotae,
erassae, pubescentes; tribus ultimis articulis vix perspicue incras-
satis. Coxaé anticae subglobosae, inter se contingentes; acetabulis
clausis. Coxae intermediae in longitudinem oblongae, parum
remotae. Metasternum elongatissimum, sulco profundo, apice
excavato, in longitudinem secatum. Coxae posticae in longitudinem,
8 M. Antoine Grouvelle on
suboblongae, postice subangulosae, valde remotae. Abdomen,
quam metasternum multo brevius, subtus inspectum abrupte valde-
que inflexum; primo segmento inter coxas posticas elevato et ante
metasterni sulcum emarginato.
Ce nouveau genre entre’ dans la tribu des Apistini;
Vinsecte trés curieux pour lequel il est établi, rappelle
jusqu a un certain point, lorsquw il est vu de dessus, wn minus-
cule Dictrillus.
5. Sarothrias eximius, n. sp. (PI. I, fig. 7.)
Subovatus, antice angustatus, convexus, nitidulus, glaber, ater;
tibiis apicem versus piceis. Antennae incrassatae, apicem versus
amplatae ; tribus ultimis articulis vix abrupte latioribus; 2° articulo
transverso, 38°-8° transversissimis, 9°-11° transversis, omnibus
pubescentibus. Caput subtriangulare, fere duplo latius quam
longius, antice subtruncatum, utrinque juxta antennarum basin
lobato-elevatum, antice inter hos lobos transversim impressum ;
oculis modice prominulis; lateribus ante oculos parallelis. Protho-
rax subparallelus, sesquilongior quam latior, tenuissime asper, parce
punctulatus, in longitudinem sulcato-striatus ; sulco antice posticeque
attenuato. Eyltra basi quam prothorax fere latiora, lateribus in
primo brevissime sinuata, dein arcuata, ampliata, apicem versus
attenuata, sinuata et apice breve truncata, magis duplo longiora
quam simy latiora, praecipue basin versus valde lineato-punctata,
substriata; lineis juxta basin vicissim in puncto valido junctis, his
punctis prothoracis basin praetexentibus. Long. 2 mill.
Subovale, environ trois fois et demie plus long que large dans sa
plus grande largeur, convexe, un peu brillant, glabre; antennes et
pattes brun de poix. Antennes épaisses; 1° article arqué prés de
la base, environ une fois et demie plus long que large aprés la courbure
de la base; 2™° subtransversal; 3™° environ deux fois plus large
que long, 4™*un peu plus court que le précédent ; 5™¢ & 8™* subégaux,
environ trois fois plus larges que longs, 9™° un peu plus long et a
peine plus large que le 8™°; 10™° et 11™° subégaux, un peu plus
longs que J™°*, le dernier un-peu plus étroit que le précédent. Téte
triangulaire, deux fois plus large au niveau des yeux que longue ;
éparsément et irréguli¢rement pointillée; cdtes paralléles relevés
chacun en lobe gibbeux, allongé, séparés par un intervalle subcon-
cave, limité en avant par une faible impression; bord antérieur
subtronqué; yeux assez saillants, placés au dessous de la base des
antennes et séparés de celles-ci par un vague sillon antennaire. Pro-
thorax faiblement bisinué de chaque cdté, paralléle, plus convexe
Coleoptera of the families Osiomidae, Monotomidae, etc. 9
en avant qu’a la base, environ aussi large que la téte au niveau des
yeux, une fois et demie plus long que large, éparsément pointillé,
coupé dans la longueur par une strie sulciforme, atténuée aux extré-
mités; bord antérieur arqué en avant, base saillante anguleusement
en arri¢re au milieu; bords latéraux arrondis, marges latérales
fortement infléchies, biimpressionnés. Ecusson trés petit, oblong,
allongé. Elytres émoussés aux épaules, alors un peu plus larges que
le prothorax a la base, trés briévement sinués, puis arqués, élargis,
présentant leur plus grande largeur vers le milieu de la longeur,
longuement sinués et atténués vers lextrémité, bri¢évement sub-
tronqués ensemble au sommet. Ponctuation grosse, disposée en
lignes substriées, attenuée vers le sommet; intervalles étroits, un
peu relevés; lignes réunies deux & deux a la base, dans un gros point ;
ces divers points placés dans une large impression sulciforme bordant
la base. Extrémité des élytres bri¢vement infléchie, subtronquée ;
stries suturales enfoncées au sommet. Métasternum éparsément
pointillé de chaque cété du sillon longitudinal. Extrémité de ’abdo-
men brun de poix clair. Pattes robustes; tibias antérieurs et inter-
médiaires munis a langle apical interne d’une épine recourbie,
saillante latéralement; tibias postérieurs prolongés a cet angle par
une petite épine.
4 exemplaires.
Loc. SEYCHELLES. Silhouette : ‘ High forest near Mont
Pot-a-eau, ca. 1500 feet, and above Mare aux Cochons,
over L000 feet, vill.ix. 1908.”
PYCNOMERINI.
Pycnomerus, Erichson, 1848, in Wiegm. Arch. I, p. 214.
subg. Penthelispa, Pascoe, 1860, Journ. of Ent. J,
Daal DE
6. Pyenomerus (Penthelispa) confertus, Reitter.
Penthelispa conferta, Reitter, 1878, Deutsche Ent. Zeitschr.,
Pat2o.
Le type de l’espéce provient de Madagascar. P. conferta, Reitt.,
est trés variable, comme taille, comme épaisseur des antennes et
sculpture du prothorax. Sa caractéristique générale se réduit a:
antennes courtes, articles 2™° et 3™° transversaux, 4™¢ a 9™e trés
transversaux; pronotum couvert dune ponctuation irrégulicrement
serrée, assez forte, en général un peu allongée, laissant libre, sur la
moitié basilaire, un petit espace longitudinal; disque plus ou moins
10 M. Antoine Grouvelle on
biimpressionné. Stries des élytres bien marquées, fortement ponc-
tuées; intervalles plus étroits que les stries. La forme voisine dans
la faune indienne est P. nitidicollis, Reitt. Chez cette espéce la
ponctuation du prothorax est en général un peu plus arrondie et
les intervalles des stries des élytres sont aussi larges que les points.
Environ 215 exemplaires.
Loc. SEYCHELLES. Mahé, Silhouette, Praslin: ‘‘ Mahé
and Silhouette, throughout the mountain-forests, 1000-2000
feet. Praslin, one specimen from Cétes d’Or Estate, x1.
1908,”
DITOMINI.
Diroma, Herbst, 1793, Kafer, V, p. 26.
7. Ditoma eavicollis, n. sp. (Pl. I, fig. 6.)
Elongata, parallela, convexa, vix nitidula, flavo-pubescens,
ferruginea. Antennae breves, Jl-articulatae; clava 3-articulata,
le articulo quam 2° angustiore. Caput modice transversum, antice
truncatum, inter antennarum bases profunde biimpressum et juxta
basin reflexo-elevatum; fronte inter oculos dense punctato; epis-
tomo crebre et vix perspicue punctulato; oculis magnis, modice
prominulis, Prothorax subquadratus, lateribus tenuiter crenulatus,
utrinque in longitudinem extus carinatus, retro intus hebetato-
subearinatus; intervallis: 1° inter latera et carinas concavis, fere
bilineato-granosis; 2° inter carinas et elevationes hebetatas juxta
carinam profunde impressis; 3° inter elevationes hebetatas antice
valde longeque impresso et juxta basin triimpresso. Elytra circiter
2 et 4 longiora quam simul Jatiora, in disco quadri-carinata : suturali
et 1* dorsali integris, 2” dorsali et humerali fere juxta apicem evanes-
centibus; intervallis carinarum bilineato-punctatis; punctis sub-
quadratis. Long. 2 mill.
Paralléle, environ trois fois et trois quart plus long que large,
convexe, & peine brillant, ferrugineux, couvert d’une pubescence
flave rappelant celle des Ditoma. Antennes de onze articles, ter-
minées par une massue de trois articles; 1° article cylindrique, un
peu plus long que large, 2™° un peu moins épais, 3™° a 7™° progres-
sivement un peu plus épais, 3™° un peu allongé, 4™¢° a 8™* serrés, les
trois premiers plus transversaux que le dernier; 1 article de la
massue plus étroit * que les suivants, le dernier subglobuleux, environ
* D’aprés les auteurs, Ditoma crenata, Herbst, type du genre
Ditoma, v’a pas de sillons antennaires et a les antennes terminées
par une massue de deux articles. En réalité cet insecte a des rudi-
ments de sillons antennaires qui permettent aux antennes de venir
s étendre dessous la téte pendant la position de repos, et ses antennes
Coleoptera of the families Ostomidae, Monotomidae, etc. 11
deux fois plus long que les précédents. Téte un peu moins de deux
fois plus large au niveau des yeux que longue, tronquée au bord
antérieur, relevée de chaque coté contre la base de Vantenne et le
bord interne de Voeil, marquée contre ce relcvement, entre les yeux,
par une impression striée oblique, arquée en dedans & la base, plus
accentuée devant l’antenne et se réunissant en arricre par l’intermédi-
aire dune faible impression arquée & VPimpression correspondante ;
front subdéprimé, densément ponctué; épistome transversalement
convexe, opaque; yeux gros, échancrant a peine les marges latérales
du front. Prothorax subcarré, 4 peine plus large que long, finement
erénelé sur les bords latéraux, marqué dans la longueur de quatre
élévations granuleuses; les deux externes caréniformes, réfléchies
contre le bord antérieur; les deux internes trés légcrement flexueuses,
caréniformes contre le bord antérieur, puis largement obtuses, se
dilatant avant la base, enfermant alors une impression allongée et
atteignant le sillon marginal de la base; intervalles: 1° entre les
bords latéraux et les carénes latérales concaves, marqués dune double
ligne de granulations presque réguliére ; 2° entre les carénes latérales
et les élévations internes, larges en avant contre le bord antéricur,
rétrécis lorsque les élévations internes deviennent obtuses: 3™*
entre les élévations internes, granuleux, largement et assez pro-
fondément excavé en avant, trés étroit entre les dilatations basilaires
des élévations internes; base bordée par un sillon entre les carénes
latérales. Ecusson petit, suborbiculaire. Elytres environ deux
fois et demie plus longs que larges, arrondis ensemble au sommet,
carénés comme ceux des Ditoma; carénes suturales et 1°'’s dorsales
entiéres, 2™¢ dorsale et humérale s’arrétant trés prés du bord mar-
ginal; lignes de points des intervalles des carénes séparées par un
intervalle égal aux points, ceux-ci subcarrés. Marges latérales avec
deux lignes de points, une caréne entiére et une ligne marginale de
points. Sillons antennaires nuls; yeux gros, entaillant fortement les
marges latérales-inférieures de la téte.
2 exemplaires.
Loc. SEYCHELLES. Silhouette: ‘‘ Forest near Mare aux
Cochons, ca. 1000 feet, viil.—ix. 1908.”
ont une massue de deux articles préparée par un article beaucoup plus
étroit que la massue décrite par les auteurs, mais nettement plus
large que l’article précédent. Enfin les yeux s’étendent en dessous
de la téte, alors que chez les T'rionus, Fairm., anciens Ditoma a sillons
antennaires, ils se trouvent limités par ce sillon et sont par suite
enticrement latéraux.
Les Xuthia, Pase., présentent les mémes caractéres et sont en fait
trés rapprochés des Ditoma type crenata. Ils ont le bord latéral du
prothorax épais, silloné,
12 M. Antoine Grouvelle on
XuTHIA, Pascoe, 1863, Journ. of Ent., I, p. 28, pl. 8, f. 1.
8. Xuthia sicana, Pascoe.
Xuthia sicana, Pascoe, 1863, 1. ¢.
Xuthia maura, Pascoe, 1863, |. ¢.
Xuthia rufina, Pascoe, 1863, |. ¢.
Espéce répandue dans toutes les Indes orientales; trés
variable.
66 exemplaires.
Loc. SEYCHELLES. Silhouette, Mahé, Félicité: “ Suil-
houette; sixty specimens from under bark of felled trunks
of a dicotyledonous tree, near the coast at Pointe Etienne,
17. 1x. 1908; also four specimens from elevations of 1000 feet
or more. Mahé, one specimen from Mare aux Cochons
district, 1000-2000 feet, 1. 1909. Félcité, one specimen
from forest, xu. 1908.”
Ciconegs, Curtis, 1826, Brit. Ent., IV, f. 149.
9. Cicones scotti, n.sp. (PI. I, fig. 9.)
Ovatus, modice convexus, nitidulus, squamulis plus minusve
albido-ochraceis, ex parte infuscatis vestitus, brunneus; elytris
ochraceo-testaceo-variegatis, antennis clava excepta piceo-testaceis,
pedibus dilutioribus. Antennae breves; clava globosa, quam articulis
praecedentibus multo latiore. Caput modice transversum, antice
sinuatum, fronte depressum, antice, inter oculos, utrinque oblique
substriolatum; fronte tenuiter punctulata, subdense squamosa;
oculis elongatis, parum prominulis. Prothorax antice quam postice
angustior, lateribus arcuatus, circiter in maxima latitudine sesqui-
latior quam longior; margine antico medio rotundato-producto,
utrinque sat valde sinuato; angulis anticis subacutis; lateribus antice
subsinuatis, vix perspicue crenulatis, tenuissime ciliatis: angulis
posticis obtusis; basi utrinque late subsinuata, tenuiter. striato-
marginata, praecipue medio ciliata; disco plus minusve dense tenuis-
simeque punctulato, dense squamoso, aliquibus squamulis obscuris
intermixtis. Elytra humeris subangulosa, lateribus arcuata, ampli-
ata, apice conjunctim subacuminata, circiter sesquilongiora quam
in maxima latitudine latiora, striato-punctata ; intervallis latis,
unilineato-punctulatis, praecipue ad basin transversim vix striolatis ;
squamulis validioribus in intervallis, minoribus in striis instructis ;
squamulis infuscatis in partibus obscurioribus praecipue congregatis.
Long. 2-2°7 mill.
Coleoptera of the families Ostomidae, Monotomidae, etc. 13
Ovale, atténué vers Pavant, environ deux fois et demie plus long
que large dans sa plus grande largeur, modérément convexe, un peu
brillant, couvert de squamules blanchatres ou d@’un jaune-blanchatre
entremélées de squamules foncées, localisées, sur les élytres, sur la
partie foncée du tégument; brun un peu rougeatre, varié sur les
élytres de taches, testacées, un peu ferrugineuses. Antennes courtes ;
1 article épais, un peu plus long que large; 2™* encore épais, une
fois et demie plus long que large; 3™° plus de deux fois plus long
que large, 4™° allongé, 5™* 4 9™° progressivement un peu plus épais,
5”¢ subcarré, les autres subégaux, 10™° subglobuleux, un peu plus
long que large, plus de quatre fois plus large que le précédent, bordé
sauf contre l’insertion avec l’article précédent par une marge feutrée.
Téte nettement moins de deux fois plus large au niveau des yeux
que longue, sinuée au bord antérieur, déprimée sur le front, finement
pointillée, densément couvert de squamules allongées, couchées,
orientées dans la longueur, serrées, bordant Vorbite des yeux et
entremélées de quelques squamules plus petites; yeux allongés,
peu saillants, échancrant modérément les marges latérales du front;
épistome un peu convexe, trés densément et trés finement pointillé,
séparé du front par deux faibles strioles obliques; labre assez grand.
Prothorax un peu plus rétréci en avant qu’a la base, arrondi sur les
cotés, présentant sa plus grande largeur un peu au dela du milieu
de la longueur a partir de la base; bord antérieur subtronqué,
assez fortement sinué de chaque cété, cilié plus fortement au milieu ;
angles antérieurs aigus, un peu saillants en avant, cdtés trés briéve-
ment sinués en avant, 4 peine visiblement crénelés, trés finement
ciliés; angles postérieurs obtus; base arrondie au milieu, sinuée de
chaque cdoté, étroitement rebordée-striée, ciliée au milieu; squamules
serrées, couvrant la majeure partie du pronotum, laissant libres,
de chaque cdté, trois petits espaces mal definis: le premier longi-
tudinal, prés du milieu, sur la moitié basilaire de la longueur, le 2™°
allongé, contre la base, plus prés de Pangle postérieur que du milieu,
le 3™° sur le prolongement du 2™*, sur la moitié antérieure du disque ;
squamules en général transversales ou subtransversales en avant,
obliques en arriére. Ecusson trés transversal, largement arrondi
au sommet, bordé de squamules a la base. Elytres un peu plus
larges & la base que le prothorax, & peine arrondis aux épaules,
arqués sur les cotés, présentant leur plus grande largueur vers le
premier tiers de la longueur a partir du sommet, atténués ensuite vers
Pextrémité et subacuminés ensemble au sommet, striés-ponctués.
Stries atténuées vers le sommet; intervalles larges, subondulés,
chacun avec une ligne de petits points. Squamules fortes placés
sur les intervalles des stries; squamules plus faibles placées sur les
stries; squamules claires dessinant principalement: 1° une tache
14 M. Antoine Grouvelle on
scutellaire; 2° une bande arquée, partant sur chaque élytre de
l’épaule et atteignant presque la suture; 3° aprés et contre le milieu
une bande transversale, plus ou moins interrompue, remontant sur
la suture; 4° une bande transversale, antéapicale, tres atténuée
sur la suture; 5° une tache apicale. Marges latérales étroitement
réfléchies, bordées par une frange de petites squamules. Dessous
du corps brun rougeatre; sillons antennaires convergents.
15 exemplaires.
Loc. SEYCHELLES. Silhouette: ‘From forests near
Mont Pot-i-eau and Mare aux Cochons, between 1000 and
2000 feet, vill.—ix. 1908.”’
10. Cieones compactus, n.sp. (PI. II, fig. 16.)
Vix ovatus, convexus, opacus, nigro-brunneus, antennis, pedibus
et prothoracis marginibus reflexis “rufo-testaceus, setis squami-
formibus, brevissimis, albido-ochraceis vestitus. Antennae breves,
eraciles; 3° articulo subquadrato, clava glandiformi, sesquilongiore
quam latiore, fere quater latiore quam 9° articulo. Caput trans-
versum, fronte depressum, antice subtruncatum, parce punctulatum
et squamosum; marginibus lateralibus squamoso-ciliatis. Pro-
thorax antice quam postice parum magis angustatus, lateribus extra
basin valde rotundatus, modice arcuatus, in maxima latitudine paulo
magis duplo latior quam longior; margine antico medio arcuato
utrinque sinuato, breviter squamoso-ciliato; angulis anticis sub-
rectis, hebetatis; lateribus sublate concavo-explanatis, tenuiter
ciliatis; angulis posticis rectis; basi medio arcuata, utrinque late
sinuata, sulco et linea squamosa marginata; disco ante basin quatuor
impressionibus laevibus, magnis, notato; squamulis praecipue
circa impressiones densatis. Elytra humeris rotundata, tune quam
prothorax vix latiora, apicem versus subrecte parum ampliata,
dein arcuata et apice conjunctim late subacuminata, fere sesqui-
longiora quam simul in maxima latitudine latiora; squamulis ineato-
dispositis. Long. 1°5 mill.
A peine ovale, atténué vers avant, presque deux fois et demie
plus long que large dans sa plus grande largueur, convexe surtout
sur les élytres, opaque, brun noiratre sur les élytres, un peu rougeatre
sur la téte et le prothorax; marges réfléchies de ce dernier, antennes
et pattes roux testacé; vestiture composée de squamules courtes,
jaune-blanchatres, disposées en lignes sur les élytres. Antennes
courtes, gréles; 1 article épais, plus long que large, caché lorsque
Vinsecte est vu de dessus, 2™° encore épais, subcarré; 3™° et 4me
subcarrés, 5™¢ & 9™e transversaux; 9™° a peine plus large que 8™,
massue glandiforme, environ une fois et demie plus long que large,
Coleoptera of the families Ostomidae, Monotomidae, etc. 15
presque quatre fois plus large, dans sa plus grande largeur, que 9™°.
Téte environ deux fois plus large au niveau des yeux que longue,
déprimée, subtronquée au bord antérieur, légérement élargie en
avant des yeux; tres opaque, couverte de squamules espacces et
bordée sur les marges latérales par une frange de squamules serrées ;
yeux échancrant les marges latérales du front, allongés, peu saillants,
leurs bords internes convergents en avant. Prothorax un peu plus
rétréci en avant qu’a la base, arqué sur les cdtés, un peu plus de
deux fois plus large dans sa plus grande largueur que long; bord
antérieur arrondi dans le milieu, sinué de chaque cdté, cilié; angles
antérieurs 4 peine aigus, émoussés; cdtés finement ciliés; marges
latérales assez largement explanées-concaves; angles postérieurs
droits; base arrondie au milieu, longuement sinuée de chaque cdté,
bordée par un sillon et par un bourrelet portant une ligne de squam-
ules; disque fortement convexe contre le sillon basilaire, marqué sur
la moitié basilaire de quatre impressions oblongues, allongées, assez
rapprochées, peu profondes, les deux externes moins accentués, et
sur le milieu du disque, en avant, dune petite impression égale-
ment oblongue et allongée; squamules assez serrées, laissant libre
Yimpression antérieure et les deux impressions médiaires posté-
rieures. Ecusson petit, suborbiculaire. Elytres arqués de chaque
cdté a la base, arrondis aux épaules, & peine arqués ensuite sur les
cotés et un peu élargis, présentant leur plus grande largeur vers le
deuxiéme tiers de la longueur 4 partir de la base, atténués vers
Pextrémité sur le dernier tiers de la longueur, et largement sub-
acuminés ensemble au sommet, presque une fois et demie plus longs
que larges ensemble, couverts de squamules disposées en lignes sur
le disque et bordant la base; intervalles larges, chacun avec une
ligne de gros points et de trés petites soies; marges latérales étroite-
ment réfléchies, finement ciliées. Dessous du corps brun rougeatre.
Sillons antennaires allongés, convergents. Saillie prosternale
carénée. Cavités des hanches antérieures ouvertes. Hanches
intermédiaires et postérieures assez écartées; saillie du premier
segment de Vabdomen arrondie. 3™° segment de Il’abdomen
échancré au sommet. Pattes gréles; tibias sans épine terminale.
1 exemplaire.
Loc. SeycHevies. Mahé: ‘ Cascade Estate, about 1000
feet, 1908.”
COLOBICONES, nov. gen.
Antennae 10-articulatae; clava uniarticulata, globosa. Sulci
antennarum nulli. Mandibulae productae, apice bicuspes. Tem-
pora elongata; capitis anguli postici obtusi. Prothorax utrinque
16 M. Antoine Grouvelle on
in longitudinem granoso-bilineatus. Elytra punctato-striata. Coxae
anticae intermediaeque valde admotae. Abdominis segmenta apice
truncata; 1° inter coxas posticas acuto-producto; ultimo excavato.
Tibiae lineares, apice spina minima armatae.
Ce nouveau genre appartient a la tribu des Ditomini;
il vient se placer entre les Cicones, les Ditoma et les Colobicus.
11. Colobicones singularis, n.sp. (PI. I, fig. 8.)
Oblongo-elongatus, fere 3 et % longior quam latior, convexus,
nitidulus, ferrugineus, setis flavis erectis sat elongatis parcissime
vestitus. Antennae subbreves; articulis 3°-9° densatis, plus min-
usve transversis; 10° subgloboso, apice pubescenti. Caput fere
tam elongatum quam latum, antice attenuatum, apice latissime
arcuatum, inter oculos transversim impressum et granoso-lineatum ;
fronte convexiuscula, in longitudinem pluribus sulcis vix impressis
secata. Prothorax antice quam postice vix angustior, lateribus
subrectus, 1 et 4 latior quam longior, in maxima parte tuberculis,
magnis, depressisimis, densatis, ocellatis instructus, utrinque in
longitudinem granoso-bilineatus; margine antico medio subarcuato,
ad extremitates sinuato; angulis anticis subacutis; lateribus vix
undulatis; angulis posticis obtusis, vix perspicue spinosis; basi
arcuata, suleo punctato marginata. Scutellum minutissimum,
laeve. Elytra subparallela, apice conjunctim subacuminata, circiter
2 et } longiora quam simul latiora, punctata-striata; punctis juxta
apicem attenuatis; intervallis striarum in disco quam punctis
parum angustioribus; striis suturalibus praecipue ad apicem magis
impressis. Long. 1°5 mill.
Allongé, un peu oblong, presque trois fois et deux tiers plus long
que large dans sa plus grande largeur, convexe, un peu brillant,
ferrugineux, présentant sur la partie postérieure des élytres * des
poils flaves, dressés, assez longs, trés espacés. Antennes assez
courtes, insérées contre les yeux; 1 article environ une fois et
demie plus long que large, 2™° un peu plus long que large, 3™° a
peine plus long que large, 4™° 4 9™° subégaux, transversaux, 10™°
subglobuleux, environ trois fois plus large que le 9™° article, terminé
par une calotte pubescente. 'Téte subovale, moins de deux fois
plus large au niveau des yeux que longue, trés largement arquée
au bord antérieur, coupée entre les yeux par une impression large,
peu profonde, marquée d’une ligne de granulations; région en avant,
* The erect hairs are most noticeable on the posterior part of the
elytra, but are present also on other parts of the body, as indicated
in the figure.
Coleoptera of the families Ostomidae, Monotomidae, etc. 17
de cette impression transversalement relevé entre les naissances
des antennes, présentant & la base deux petits tubercules, région en
arri¢re présentant de chaque cdté quatre courtes carénes longi-
tudinales peu accentuées; yeux petits, non saillants; tempes plus
longues que les yeux, subparalléles; angles postérieurs obtus; labre
subtrapézoidal, environ trois fois plus large 4 la base que long. _ Pro-
thorax un peu plus large en avant qu’a la base, trés faiblement arqué
sur les cotés, environ une fois et un tiers plus large que long, couvert,
sauf sur le milieu de la marge antérieure, de gros tubercules trés
déprimés, ocellés et serrés, présentant de chaque cdté deux lignes
rapprochés de granulations; ligne externe un peu plus accentuée
que Tinterne, atteignant la base, infléchie en dedans au sommet;
ligne interne éffacée a la base; bord antérieur un peu arqué dans le
milieu, bri¢vement et assez fortement sinué vers les extrémités,
bordé au milieu par une ligne de petites granulations; angles
antérieurs aigus, un peu saillants en avant; bords latéraux légére-
ment ondulés, armés de quelques soies dressées; angles postrieurs
obtus; base arquée en arriére, bordée par un assez fort sillon ponctueé.
Ecusson trés petit, lisse. Elytres bri¢vement arrondis aux épaules,
arqués sur les cotés, & peine élargis, bri¢évement arrondis ensemble
au sommet, environ deux fois et un quart plus longs que larges
ensemble dans leur plus grande largeur, assez fortement ponctués
en lignes, substriés; points atténués contre le sommet et vers les
marges latérales; intervalles discoidaux, au plus aussi larges que
les points; stries suturales relativement enfoncées, surtout sur le
disque. Menton présentant a la base trois courtes carénes longi-
tudinales. Prosternum et métasternum grossiérement, peu pro-
fondément et densément ponctué. Abdomen presque lisse.
1 exemplaire.
Loc. SryYcCHELLES. Mahé: “Cascade Estate, about
1000 feet, 1908.”
Dretotoma, Erichson, 1845, in Germar, Zeitschr., p. 25
note 4.
7,
12. Diplotoma eapito, n.sp. (PI. II, fig. 11.)
Suboblonga, convexa, nitidula, ferruginea, capite subinfuscata,
se‘is squamiformibus, brevissimis, albido-ochraceis vestita. An-
tennae subgraciles; 3° articulo parum elongato; clava bi-articulata,
fere duplo longiore quam latiore, 2° articulo quam primo angustiore.
Caput transversum, convexiusculum, antice breviter subtruncatum,
subdense squamosum; marginibus lateralibus antice squamoso-
ciliatis. Prothorax antice quam postice paulo angustior, lateribus
TRANS. ENT. SOC. LOND. 1918.—PARTS I, Il. (DEC.) C
18 M. Antoine Grouvelle on
antice rotundatus, postice longe subarcuatus, circiter duplo latior
quam longior, praecipue ad marginis antici medium subdense
squamosus; margine antico arcuato, ciliato, ad extremitates vix
sinuato; angulis anticis fere rotundatis; lateribus tenuiter margin-
atis, ciliatis; angulis posticis obtusis; basi medio subangulose pro-
ducta, utrinque sinuata, sulco et pulvino squamoso marginata.
Scutellum infuscatum. Elytra humeris vix perspicue angulosa,
lateribus arcuata, parum ampliata, apice conjunctim late sub-
acuminata, fere sesquilongiora quam simul in maxima. latitudine
latiora; squamulis lineato-dispositis. Long. 1°4 mill.
Suboblong, atténué vers Pavant, environ deux fois et demie
plus long que large dans sa plus grande largueur, convexe, un peu
brillant; ferrugineux, assombri sur le front et sur lécusson, plus
clair sur les antennes et les pattes, couvert de squamules blanchatres,
disposées en lignes sur les élytres. Antennes courtes, modérément
gréles; It" article épais, allongé, caché lorsque Vinsect est vu de
dessus, 2™° encore épais, un peu allongé, 3™° subcarré, 4™° a 9™°
progressivement plus transversaux, 10™° et 11™° formant une
massue environ deux fois plus longue que large, dont le 1 article
est environ trois fois plus large en avant que le 9™° article, et dont le
dernier article, plus étroit que le 10™°, est suboblong. Téte grosse,
égale en longueur environ aux deux tiers de la longueur du prono-
tum, environ deux fois plus large au niveau des yeux que longue,
légérement convexe, briévement subtronquée au bord antérieur,
assez saillante en avant des bases des antennes, assez densément
couverte de squamules; bords latéraux trés convergents en avant
des bases des antennes, modérément entre les antennes et la base
des yeux, échancrés par ceux-ci, ciliés surtout en avant; yeux
plutot gros, médiocrement saillants. Prothorax un peu plus rétréci
en avant qu’a la base, arrondi sur les cétés, puis longuement sub-
arqué, faiblement atténué ves la base, environ deux fois plus large
dans sa plus grande largeur que long; bord antérieur faiblement
arqué, trés bric¢vement sinué aux extrémités, assez longuement cilié
dans le milieu; angles antérieurs presqu’ arrondis; cotés ciliés et
étroitement rebordés par un fin bourrelet limité en dedans par une
ligne de squamules allongées; angles postérieurs obtus; base
saillante anguleusement en arriére dans le milieu, longuement sinuée
de chaque cdté, bordée par une ligne de squamules et un sillon droit ;
disque assez fortement et trés bri¢vement convexe contre le sillon
basilaire, assez densément couvert de squamules dessinant un point
de convergence vers le milieu du bord antérieur, squamules laissant
libre de chaque cdté contre la bordure latérale une marge relative-
ment large. Ecusson petit, suborbiculaire. Elytres arrondis
Coleoptera of the families Ostomidae, Monotomidae, etc. 19
séparément a la base, arrondis aux épaules, & peine visiblement
anguleux, alors un peu plus larges ensemble que le prothorax dans
sa plus grande largeur, s’élargissant presqu’ en ligne droite jusqu’au
deuxiéme tiers de la longueur a partir de la base, puis arqués-atténués
vers Pextrémité et largement subacuminés ensemble au sommet,
presqu’ une fois et demie plus longs que larges ensemble dans leur
plus grande largeur, ponctués en lignes; squamules disposées en
ligne sur les intervalles. Marges latérales fortement infléchies ;
ligne ponctuée marginale plus marquée, un peu enfoncée; bord
marginal bordé par un fin bourrelet squameux. Dessous du corps
ferrugineux, un peu rougedtre; poitrine enfoncée. Sillons anten-
naires nuls. Cavités des hanches antérieures ouvertes. Saillie du
premier segment de abdomen entre les hanches postérieures aigue,
émoussée. Pattes linéaires; tibias sans épine apicale.
1 exemplaire.
Loc. StkYCHELLES. Mahé: ‘ From stunted forest vege-
tation on summit of Mount Sebert, about 1800 feet, 1.
T9097;
Neorricuus, Sharp, 1885, Journ. Linn. Soc. Lond., Zool.,
EX pe G0:
13. Neotrichus gardineri, n. sp.
Elongatus, subparallelus, modice convexus, opacus, setis flavis,
brevissimis parce vestitus, ater, antennis extra ultimum articulum
pedibusque rufo-fuscis. Antennae breves, 10-articulatae, ultimo
articulo obeonico, apice pulvino minimo dilutiore instructo. Caput
transversum, lateribus antrorsum attenuatum, antice medio trun-
catum et ad extremitates sinuatum, sat dense tenuiterque granosum ;
oculis modice prominulis; temporibus nullis. Prothorax antice
capite latior, lateribus rectus, basin versus parum angustatus, in
maxima latitudine paulo longior quam antice latior, densius et
validius quam caput granosus; margine antico antrorsum arcuato,
utrinque sat valide sinuato; lateribus denticulatis, denticulis basin
versus paulatim majoribus; basi retrorsum arcuata, sulcato-
marginata. Scutellum minimum, subtrapezoidale. Elytra basi
quam prothorax latiora, 3 et $ longiora quam simul latiora, apice
separatim breviter rotundata, punctato-striata; punctorum inter-
vallis transversim striolatis; setis in striarum intervallis insertis.
Long. 3°5-4°5 mill.
Allongé, subparalléle, modérément convexe, ¢troitement déprimé
sur le disque des élytres, opaque, noir avec les antennes sauf le
dernier article roux-enfumé, couvert de soies flaves, dressées, trés
20) . M. Antoine Grouvelle on
courtes, insérées sur les intervalles des stries des élytres. Antennes
courtes, de 10 articles, terminées par une massue d’un article; 1°
article subcarré, épais, caché lorsque Vinsecte est vu de dessus, 2™°
encore épais, suborbiculaire, 3"° plus de deux fois plus long que
large, 47° et 5™° subglobuleux, 6™* A 8™° a peine plus étroit que les
précédents, transversaux, oblongs, 9™° 4 peine plus long et a peine
plus large que 8™*, 10™* en forme de trone de céne renversé, sensible-
ment aussi long que large en avant, au moins deux fois et demie
plus large en avant que le 9™° article, terminé par un petit bouton
plus clair, cylindrique. Téte presque deux fois plus large au niveau
des yeux que longue, subtronquée au milieu du bord antérieur et
sinués de chaque cdté, droite sur les cétés et atténuée en avant,
déprimée et couverte de granulations serrées, assez fines sur le front,
presqu’ impressionnée en arc entre les bases des antennes et infléchie-
déprimée; éparsément ponctuée en avant de cette impression.
Yeux moyens, a peine pubescents, n’échancrant pas les marges
latérales du front, un peu saillants. Sillons antennaires légérement
convergents. Prothorax plus large en avant que la téte, faiblement
rétréci vers la base, environ aussi long dans sa plus grande longueur
que large en avant, couvert de granulations plus fortes et un peu plus
serréss que celles de la téte; bord antérieur arqué en avant, assez
profondément sinué de chaque cété, trés légérement relevé en
bourrelet vers les extrémités; angles antérieurs aigus, émoussés,
saillants en avant; cdtés droits, armés de denticules trés fins et
trés serrés en avant, progressivement plus forts et plus espacés vers
la base; marges latérales fortement infléchies, surtout au milieu,
bordées par la denticulation; angles postérieurs obtus; base forte-
ment arquée en arriére, & peine subsinuée aux extrémités, étroite-
ment bordée par un sillon et par un bourrelet granuleux. Ecusson
petit, suboblong, transversal. Elytres paralléles, plus larges que le
prothorax en avant, environ trois fois et demie plus longs que larges
ensemble, briévement et séparément arrondis au sommet, assez
densément ponctués-striés; points crénelant les intervalles et leur
donnant un aspect ondulé; ceux-ci marqués d’une ligne de trés
petits points; stries des marges latérales se réunissant vers le
sommet aux stries discoidales et enfermant les stries des régions
humérales et subhumérales; marges latérales trés fortement in-
fléchies, étroitement bordées par une strie marquée de gros points
espacés. Dessous du corps brun rougedtre, densément et peu
profondément ponctué; dernier segment de VPabdomen concave.
Tibias linéaires, sans épines & l’extrémité
3 exemplaires.
Loc SrycHeties. Silhouette, Mahé: “ Silhouette, one
Coleoptera of the families Ostomidae, Monotomidae, ele. 21
specimen from the high forest near Mont Pot-d-eau, ca.
1500 feet, and one from a low elevation near Pointe Etienne,
vill.-ix. 1908. Mahé, one specimen from Cascade Estate,
at about 1000 feet.”
14. Neotrichus parallelocollis, n. sp.
Elongatus, parallelus, modice convexus, subopacus, setis brevis-
simis, squamiformibus, in elytris lineato-dispositis, flavis vestitus,
nigricans; pedibus fusco-rufis, antennis dilutioribus. Antennae
subbreves, 10-articulatae; ultimo articulo obconico, apice pulvine
minimo instructo. Caput transversum, lateribus antrorsum attenu-
atum, antice medio truncatum et ad extremitates sinuatum, sub-
dense tenuiterque granosum, inter antennarum bases oblique
biimpressum; oculis parum productis. Prothorax antice capite
latior, lateribus parallelus, fere in maxima latitudine tam longior
quam latior, densius et paulo validius quam caput granosus ; margine
antico antrorsum arcuato, ad extremitates sinuato, pulvinato-
marginato; lateribus tenuiter denticulatis, denticulis basin versus
paulatim majoribus; basi retrorsum arcuata, vix perspicue sulcato-
marginata. Scutellum minimum, suboblongum. Elytra basi pro-
thorace paulo latiora, fere ter longiora quam simul latiora, apice
vix separatim breviter rotundata, stricte et sat profunde punctato-
striata; striarum intervallis transversim striolatis et irregulariter
bilineato-granosis. Long. 3°7 mill.
Allongé, paralléle, modérément convexe, étroitement subdéprimé
sur le disque des élytres, 4 peine brillant, noiratre; avec les pattes
roux-enfumé et les antennes plus claires, couvert de soies squami-
formes, flaves, trés courtes, dressées, disposées en lignes sur les
élytres. Antennes médiocrement courtes, de 10 articles, terminés
par une massue d'un article; 1 article épais, subcarré, caché lorsque
linsecte est vu de dessus, 2™¢ encore ¢pais, suboblorg, un peu plus
long que large, 3™° presque trois fois plus long que large, 4™° a 9me
* s’épaississant faiblement et progressivement, subégaux, trans-
versaux, 10™° presqu’en forme de trone de cone renversé, environ
deux fois aussi large en avant que Varticle précédent et aussi long
que large en avant, terminé par un petit bouton cylindrique. 'Téte
environ deux fois plus large au niveau des yeux que longue, sub-
tronquée au milieu du bord antérieur et sinuée aux extrémités,
droite sur les cétés et atténuée en avant, déprimée sur le front,
couverte de granulations assez serrées, fines, marquée de chaque
cdoté entre les bases des antennes d’une forte impression arquée en
dedans, ponctuée sur la marge antéricure, Yeux moyens, a peine
22 M. Antoine Grouvelle on
pubescents, n’échancrant pas les marges latérales du front, un peu
saillants. Sillons antennaires convergents. Prothorax plus large
en avant que la téte, paralléle, environ aussi long dans sa plus
grande longueur que large, couvert de granulations plus denses
et un peu plus fortes que celles de la téte; bord antérieur arqué
en avant, trés bri¢vement sinué aux extrémités, bordé par un bourre-
let modérément accentué, dilaté dans la partie médiane; angles
antérieurs droits; cdtés droits, armés de petits denticules progres-
sivement un peu plus forts vers la base; marges latérales un peu
obliquement infléchies; angles postérieurs un peu obtus; base
arquée en arricre, bordée par un bourrelet granuleux et par un sillon,
tous deux peu marqués. Ecusson petit, oblong, transversal. Elytres
arrondis aux épaules, paralléles, alors un peu plus larges que le pro-
thorax a la base, presque trois fois plus longs que larges ensemble,
presque briévement et séparément arrondis au sommet, étroitement
et assez profondément ponctués-striés; intervalles coupés trans-
versalement par des strioles partant des points des stries; intervalles
entre ces strioles avec deux granulations irréguliéres souvent réunies,
donnant limpression lorsque Vinsecte est vu dans la longueur de
deux lignes de granulations dont Vinterne est plus accentuée.
Sculpture sur la marge basilaire réduite a des granulations disposées
en lignes, cinquiéme et onziéme intervalle de ces lignes briévement
un peu relevés. Marges latérales fortement infléchies, a peine
rebordées. Dessous du corps noiratre, densément ponctué; dernier
segment de labdomen concave. Tibias linéaires, sane épine 2
Pextrémiteé.
2 exemplaires.
Loc. SEYCHELLES. Mahé:
1000 feet.”
ee
Cascade Estate, about
Lascoronus, Grouvelle, 1895, Bull. Museum Paris, No. 4,
p- 156.
15. Laseotonus scotti,n.sp. (Pl. I, fig. 3.)
Elongatus, parallelus, convexus, opacus, setis flavis, brevibus,
erectis sat dense vestitus, nigricans; antennis pedibusque rufo-
‘uscis, elytris sordido-aurantiaco-variegatis. Antennae breves; 3°
articulo subtransverso, clava fere triarticulata, 1° articulo trans-
versissimo basi quam praecedente vix abrupte latiore, 2° quam 1°
latiore, transversissimo, 38° quam praecedente angustiore, sub-
globoso, 2° et 3° dilutioribus. Caput transversum, subparallelum,
antice medio rotundato-productum, utrinque breviter truncatum,
granosum; oculis glabris, modicissime productis, Prothorax basin
Coleoptera of the families Ostomidae, M onotomidae, etc. 23
versus vix attenuatus, 1 et } longior quam antice latior, dense
granosus; margine antico antrorsum arcuato, ad extremitates
sinuato, pulvinato-marginato, pulvino ad medium ampliato et
retrorsum angulatim producto; lateribus tenuiter denticulatis;
basi arcuata, ad extremitates subsulcato-marginata. Scutellum
minimum, oblongo-elongatum. Elytra circiter 3 et 4 longiora quam
simul latiora, apice conjunctim breviter rotundata, striato-punctata ;
intervallis planis quam punctis latioribus; setis erectis in punctis
insertis; singulo elytro duabus maculis aurantiacis notato: 1*
humerali, magna, subquadrata; 2* juxta suturam, discoidali,
elongatissima, lata, extus medio quadratim laciniata. Long. 3°5—
4°5 mill.
Allongé, paralléle, environ quatre fois et deux tiers plus long que
large, convexe, opaque, noiratre, varié sur les élytres de jaune-
orange un peu sale, couvert de soies flaves, dressées, courtes, assez
serrées, insérées sur les élytres sur les points des stries. Antennes
et pattes roux, plus ou moins un peu enfumé; les deux derniers
articles des antennes un peu plus clairs que les précédents. Antennes
courtes; 1 article court, épais, caché lorsque lVinsecte est vu de
dessus; 2™° épais, obconique, aussi long que large en avant; 3™¢
modérément transversal; 4™° & 8™° subégaux, plus courts que 3™°;
gee & 11m¢ formant une massue légérement dissymétrique, dont le
Ie" article, obconique, trés large en avant, est 4 peine plus large a
la base que le précédent, le 2™° est un peu plus long et nettement
plus large que le 1°, et le 3™° est suboblong, subégal au 2™° et plus
étroit que lui. Téte environ une fois et un tiers plus large au niveau
des yeux que longue, paralléle, largement arrondie au milieu du
bord antérieur, tronquée vers les extrémités, densément couverte
de granulations; front déprimé, trés légérement concave entre les
naissances des antennes; labre trés transversal; yeux glabres, peu
saillants; tempes petites, convergentes en avant; angles postérieurs
de la téte un peu obtus. Prothorax a peine rétréci vers la base,
droit sur les cétés, environ une fois et un cinquiéme plus long que
large, couvert de granulations déprimées, serrées, plus fortes que
celle de la téte; bord antérieur arqué en avant, sinué aux extrémités,
bordé par un bourrelet qui s’élargit vers le milieu et s’avance vers
larriére en angle obtus; cOt#s assez finement denticulés, étroitement
rebordés; base faiblement arquée vers larriére, bordée, sauf au
milieu, par un sillon peu marqué, prolongeant le sillon qui borde
les marges latérales. Ecusson petit, oblong, plus long que large.
Elytres environ trois fois et un tiers plus longs que larges ensemble,
briévement arrondis ensemble au sommet, striés-ponctués ; stries
entiéres, intervalles plans, sur le disque plus larges que les points
24 M. Antoine Grouvelle on
des stries; marges latérales trés fortement infléchies, bordées par
une forte strie ponctuée. Chaque élytre marqué de deux taches
orangées, un peu enfumées: la 1° humérale, assez grande, sub-
rectangulaire; la 2™° sur le disque, contre la suture, un peu plus
rapprochée du sommet que de la base, s’étendant environ sur la
moitié de la longueur de Vélytre, atteignant en avant et en arriére
la strie humérale et découpée au milieu du bord externe, presqu’en
carré, jusqua la 2™° strie discoidale. Dessous du corps brun
rougeatre, finement granuleux. Antennes du male un peu plus
longues et un peu moins épaisses que celles de la femelle.
Lorsque la coloration de linsecte n’est pas complétement
développée, la teinte orangée envahit plus ou moins la téte et le
pronotum.
17 exemplaires.
Loc. SkycHELLES. Silhouette: “‘ Three specimens from
near Mont Pot-a-eau, ca. 1500 feet, vii. 1908, and fourteen
specimens from under the bark of felled trees, in company
with the large series of Xuthia sicana, near the coast at
Pointe Etienne, ix. 1908.”
COXELINI.
PARALYREUS, Nov. gen.
Antennae 8-articulatae; basi occulta; clava uniarticulata,
oblonga. Sulci antennales nulli., Oculi nulli.* Coxarum anti-
carum acetabulae apertae. Metasternum et abdominis primum
segmentum aequalia. Processus intercoxale coxarum posticarum
sublatum, subtruncatum. Pedes lineares. Tarsi omnes breves,
triarticulati.
Le type de ce genre, Paralyreus scotti, est représenté par
un exemplaire unique, qui comme aspect général rappelle,
jusqu’a un certain point, les Anommatus. Sa position
eénérique parmi les Coxelini, a cdté des Lyreus, se trouve
nettement définie par linsertion des antennes cachée sous
les marges du front, l’écartement relatif des hanches pos-
térieures, l’absence de sillons et fossettes antennaires.
* The single specimen of Paralyreus scotti is entirely devoid of
metathorac wings : [ef. Cerylon curtulum and Thyroderus sculpticollis,
pp. 41, 45, footnote.] The diagnosis contains the words “oculi nulli.”
A compound microscope, however, shows that reduced eyes are
present, consisting of a single, round, simple facet on either side of
the head. They are very minute and not easy to distinguish, since
they are not black-pigmented, but of the same colour as the surs
rounding chitin,—H. S$.
bo
Or
Coleoptera of the fanulies Ostomidae, Monotomidae, eic. ‘
16. Pazalyreus scotti, n.sp. (PI. I, fig. 15.)
e /
Oblongo-elongatus, fere ter longior quam latior, convexus,
nitidus, pilis brevibus, erectis, sparsis, vix perspicuis vestitus,
testaceus. Antennae breves, 8-articulatae; 1° inecrassato, sub-
quadrato, 2° paulo angustiore, subtransverso; 3°-7° paulatim vix
incrassatis, 3° subtransverso, aliis transversis, densatis; 8° oblongo,
quam praecedente magis ter latiore, intus quam extus paulo magis
ampliato, in tribus partibus transversis diviso. Caput ad_ basin,
ante antennarum bases, sat longe sublarallelum, antice subtrian-
gulare, antice truncatum, inter antennarum bases tenuiter striatum,
parce tenuiterque punctatus; oculis deletis; labro magcno,
subhemicirculare. Prothorax postice quam antice vix angustior,
lateribus modice arcuatus, sesquilongior quam latior, parce sub-
tenuiterque punctatus, margine antico vix arcuato, angulis anticis
obtusis; lateribus tenuissime marginatis et vix perspicue crenu-
latis; basi subtruncata, tenuiter marginata. Scutellum subtri-
angulare, minimum. Elytra basi quam prothoracis basis vix
Jatiora, humeris obtuse angulosa, tune quam prothorax vix latiora,
lateribus arcuata, subampliata, apice conjunctim subacuminata,
circiter sesquilongiova quam simul latiora, confuse subdenseque
punctata; marginibus lateralibus strictissime marginatis, vix
perspicue crenulatis. Pedes tenues; tibiis limearibus. Long. 1°5 mill.
Oblong, presque trois fois plus long que large dans sa plus grande
largeur, convexe, brillant, testacé, un peu rembruni sur le milieu
de la poitrine, orné d'une pubescence peu visible formée de petits
poils, dressés, fins, espacés, visibles surtout lorsque Vinsecte est vu
de profil, Antennes tres courtes, un peu épaisses, de 8 articles;
le Ie? subcarré, épaissi, caché lorsque Pinsecte est vu de dessus, le
2me encore un peu épaissi, subtransversal, les 3™¢ & 7™° serrés,
progressivement et trés faiblement ¢paissis, 3™° subtransversal,
4me & 7™e plus ou moins transversaux, 8™° suboblong, environ une
fois et un tiers plus long que large, plus de trois fois plus large que
le sommet de larticle précédent, un peu plus dilaté en dedans
quwen dehors, partagé en trois zones successivement un peu plus
étroites, plus ou moins pubescentes, la premicre aussi longue que
les deux autres réunies. Téte environ aussi longue que large,
subparalléle a la base jusqu’a Pinsertion des antennes, triangulaire
en avant; yeux nuls; front faiblement convexe, éparsément poin-
tillé, légérement relevé de chaque cdté a la base de Pantenne, séparé
de Pépistome par une strie fortement arquée aux extrémités, celui-
ci convexe, médiocrement arrondi en avant des bases des antennes ;
labre presque demi-circulaire, cachant presque les mandibules,
26 M. Antoine Grouvelle on
celles-ci bifides 4 lextrémité. Prothorax 4 peine plus étroit A la
base qu’au sommet, un peu plus large au bord antérieur que la
téte, arqué sur les cotés, environ une fois et demie plus large dans
sa plus grande largeur que long, un peu moins éparsément et plus
fortement ponctué que le front; bord antérieur faiblement arqué;
angles antérieurs obtus, un peu émoussés; cdtés bordés par un
bourrelet trés étroit, un peu plus accentué vers la base, & peine
visiblement crénelés; vus de face sinués contre la base; angles
postérieurs obtus; base tronquée, bordée par une marge trés étroite
ponctuée vers les extrémités. Hcusson subtriangulaire, transversal.
Elytres trés faiblement un peu plus larges 4 la base que la base du
prothorax, en angle obtus aux épaules, arqués sur les cétés, & peine
élargis, a peine plus larges dans leur plus grande largeur que le
prothorax dans la sienne, acuminés ensemble au sommet, environ
une fois et demie plus longs que larges ensemble dans leur plus
grande largeur. Ponctuation relativement forte, confuse, irrégu-
licrement un peu serrée, atténuée vers le sommet. Marges latérales
subpliées, fortement infléchies, moins fortement ponctuées que le
disque, bordées par une strie ponctuée assez enfoncée. Segments
de abdomen | a 3 subégaux, plus courts que le métasternum,
soudés. Hanches postérieures un peu écartées; saillie du premier
segment de labdomen subtronquée. Tarses de quatre articles;
dernier article sans ses crochets plus long que les précédents réunis ;
crochets relativement longs, fins, dentés & la base.
1 exemplaire.
Loc. SEYCHELLES. Mahé: “ Forest between Trois Fréres
and Morne Seychellois, 1500-2000 feet, xii. 1908.”
TyrtTaEus, Champion, 1913, Trans. Ent. Soc. Lond., p. 76.
17. Tyrtaeus singularis, n.sp. (PI. I, fig. 2.)
Oblongo-elongatus, subparallelus, circiter quater longior quam
latior, modice convexus, nitidus, pilis brevibus, tenuibus, erectis,
subparce vestitus, fulvo-rufus. Antennae breves, 7-articulatae ;
articulis 2-6 paulatim incrassatis, 7° multo latiore, subelongato,
glandiformi. Caput transversum, subtriangulare, antice trun-
catum, paulo post antennarum bases transversim striatum, fronte
convexiuscula, parce tenuiterque punctulatum; labro subhemi-
circulari, mandibularum apicem fere obtegente; oculis sat magnis,
modice prominulis; temporibus nullis. Prothorax antice quam
postice vix angustior, lateribus arcuatus, in maxima latitudine
quam caput paulo latior, in disco subparece, ad latera densius,
punctulatus; margine antico subtruncato; angulis anticis obtusis,
Coleoptera of the families Ostomidae, Monotomidae, elec. 27
hebetatis; lateribus substricte marginatis; angulis posticis obtusis ;
basi tenuiter marginata. Scutellum subtriangulare. Elytra hu-
meris breviter rotundata, tune quam prothorax in maxima latitudine
vix angustiora, lateribus subparallela, apice conjunctim rotundata,
circiter 2 et $ longiora quam latiora, subregulariter lineato-punc-
tulata; punctis juxta basin et ad apicem confusis, apicem versus
attenuatis; lineis punctatis haud densatis; marginibus lateralibus
rotundato-plicatis, valde inflexis, marginatis. Long. 2°2 mill.
Subparallcle, environ quatre fois plus long que large dans sa plus
grande largeur, modérément convexe, brillant, roux fauve; ves-
titure formée de trés petits poils dressés, peu serrés, visibles surtout
lorsque Vinsecte est vu de profil. Antennes courtes, de 7 articles,
insérées presque contre les yeux, dessous le bord du front; 1° article
un peu épais, subcarré, 2™° a 6™° serrés, s’épaisissant progressive-
ment, subégaux, 2™° transversal, 6™° trés transversal, 7™° oblong,
plus de deux fois plus large que Varticle précédent 4 sa partie an-
térieure, partagé en trois zones transversales : les deux premiéres
garnies seulement de quelques trés petits poils dressés, la derniére
pubescente, ensemble donnant l’impression de trois articles soudés.
Téte transversale, subtriangulaire, rétrécie vers larriére, avant les
yeux un peu convexe et finement et éparsément pointillée sur le
front, tronquée au bord antérieur, finement striée entre les bords
antérieurs des bases des antennes, faiblement, briévement et trans-
versalement substriée entre ces bases; yeux échancrant modéré-
ment les marges du front, peu saillants; labre presqu’en forme de
demi-cercle, cachant presque complétement les mandibules. Pro-
thorax environ aussi large en avant que la téte avec les veux, a
peine plus large 4 la base, arrondi sur les cotés, présentant sa plus
grande largeur un peu en avant du milieu, environ une fois et demie
plus large dans sa plus grande largeur que long, lisse sur une étroite
bande longitudinale sur le milieu du disque, finement et presqu’
éparsément ponctué de chaque cdté de cette bande, un peu plus
fortement vers les cétés; bord antérieur subtronqué; angles an-
térieurs obtus, légérement émoussés; cdtés bordés par une strie
et un fin bourrelet subcrénelé; angles postérieurs obtus; base
tronquée, étroitement bordée par une strie dans le milieu, trés
étroitement vers les extrémités. Ecusson subtriangulaire, plutot
petit. Elytres 4 la base de la largeur de la base du prothorax,
briévement arrondis aux épaules, alors a peine plus étroites que le
prothorax dans sa plus grande largeur, subparalléles, arrondis
ensemble au sommet, environ deux fois et demie plus longs que
larges ensemble, ponctués en lignes peu serrées, un peu irrégulicres ;
ponctuation confuse prés de la base, atténuée vers le sommet;
28 M. Antoine Grouvelle on
marges latérales pliées-arrondies, puis fortement infléchies, bordées
par une trés étroite marge concave. Piece prébasilaire en angle
tres obtus au milieu, subsinuée de chaque cdté; menton petit,
subearré. Saillie prosternale dépassant les hanches, tronquée a
Vextrémité; hanches peu écartées, subglobuleuses. Métasternum
enfoncé contre les hanches intermédiaires; celles-ci peu écartées.
Hanches postérieures médiocrement écartées; saillie du 1° segment
en angle obtus; celui-ci plus court que le métasternum. 1°, 2™¢
et 3™¢ segments de labdomen soudés. Pattes médiocrement
épaisses : tibias sublinéaires, sans éperon. Tarses de trois articles.
15 exemplaires.
Loc. SkycHettes. Mahé: “ All from the forest between
Trois Fréres and Morne Seychellois, 1500-2000 feet, xi.
1908.”
COLY DIENT.
MercepanuM, Hrichson, 1845, Nature. Ins. Deutschl., III,
p. 274; Sharp, 1893, Ent. Month. Mag., X XIX, p. 256.
18. Mecedanum, sp.
Ce genre est représenté dans les collections de la Perey
Sladen Trust Expedition par deux exemplaires en mauvais
état qui ne permettent pas une détermination précise.
Loc. SEYCHELLES. Silhouette: “ Forest at edge of Mare
aux Cochons plateau, ca. 1000 feet, ix. 1908.”
CERYLINAE. BOTHRIDERINI.
BoturipEREs, Erichson, 1845, Nature. Ins. Deutschl.,. II,
p. 288.
19. Bothrideres fryeri, n. sp. (PI. I, fig. 1.)
Oblongo-elongatus, angustus, convexus, nitidulus, glaber, cas-
taneus; capite prothoraceque paulo obscurior. Antennae primo
articulo apice obliquissime truncato, 2° juxta basin valde
incurvato, 3° subquadrato; clava cireiter tam elongata quam lata,
2° articulo quam 1° paulo latiore. Caput transversum, disco sub-
concavum et subdense punctatum, marginibus anticis, posticis
lateralibusque minus valide punctatum; punctis in disco elongatis ;
oculis subhemiglobosis. Prothorax cordiformis, antice quam caput
in maxima datitudine paulo minor, 1 et + longior quam latior, dense
punctatus et in longitudinem sulco laevi striis terminato secatus ;
Coleoptera of the families Ostomidae, Monotomidae, etc. 29
sulco prope marginem anticum in impressione lata initium capiente,
in primo lato, vix profundo, postea constricto, magis impresso,
paulatim attenuato, marginem basilarem attingente. Scutellum
triangulare. Elytra basi quam prothorax latiora, humeris rotun-
data, lateribus arcuata, vix ampliata, paulo ante apicem sinuata,
fere conjunctim rotundata, 3 et 3 longiora quam simul latiora,
punctato-striata; intervallis alternis latioribus; 1° praecipue ad
apicem elevato, 2° juxta striam externam et prope apicem breviter
earinato. Long. 4 mill.
Allongé, oblong, étroit, environ cing fois plus long que large dans
sa plus grande largeur, convexe, glabre, assez brillant, marron un
peu assombri sur la téte et sur le prothorax. Antennes a peine
épaissies pour le genre; 1° article, environ aussi long que large,
fortement arrondi au bord interne, trés obliquement tronqué, sub-
sinué au sommet; deuxiéme insérée presque latéralement sur le
premier, recourbi de suite @ angle droit, presque deux fois plus long
que large, 3™° subcarré, 4™° & 7™¢ serrés, transversaux, 8™* et 9™¢ un
peu plus longs que les précédents, 10™° et 11™° formant une massue
presque lache, 4 peu prés aussi longue que large, dont le 1°" article
est environ trois fois plus large que le précédent et dont le 2™° plus
étroit et plus long que le premier est subtrapézoidal, pubescent
a Pextrémité. Téte environ deux fois plus large au niveau des yeux
que longue, tronquée en avant, subconcave entre les yeux, couverte
entre les yeux d'une ponctuation allongée, assez forte et assez
dense, en avant d’une ponctuation fine, assez serrée, sur les cétés
dune ponctuation fine, espacée; yeux saillant presqu’en forme de
demi-sphére, échancrant modérément les marges latérales du front,
non contigus au bord antérieur du pronotum. Prothorax sub-
cordiforme, & peine rétréci en avant, fortement 4 la base, presqu’
aussi large au bord antérieur que la téte au niveau des yeux, environ
une fois et un cinquiéme plus long que large dans sa plus grande
largeur; bord antérieur arrondi au milieu, sinué de chaque cdté;
angles antérieurs aigus, un peu saillants en avant; bords latéraux
cachés, sauf a la base lorsque Vinsecte est vu de dessus; angles
postérieurs presque droits; base bordée par un bourrelet et par une
strie trés bri¢vement interrompue au milieu. Ponctuation assez forte,
assez serrée, sauf sur la région des angles postérieurs. Disque coupé
longitudinalement par un enfoncement en partie sulciforme, com-
mencant en avant par une large impression & bords non marqueés,
presque contigue au bord antérieur, se continuant par un sillon
assez large, lisse au fond, peu profond, limité par des stries, com-
mencant dans impression antérieure, se rétrécissant vers le dernier
quart de la longueur et se continuant au fond par un sillon étroit,
30 M. Antoine Grouvelle on
enfoncé, atténué vers la base, qui n’atteint pas tout a fait le rebord
marginal de celle-ci. Ecusson triangulaire, un peu plus long que
large, et un peu enfoncé. Elytres largement arrondis aux épaules,
alors nettement plus larges que le prothorax dans sa plus grande
largeur, subparalléles, & peine élargis, puis atténués lentement vers
Pextrémité, sinués prés du sommet et arrondis ensemble; bordés
i Pextrémité, aprés le sinus par un bourrelet bien marqué. Sur le
disque & partir de la suture: 1°, un intervalle sutural, assez large,
trés finement ponctué en ligne; 2°, une strie ponctuée, enfoncée,
commencant prés de la base, s’accentuant vers le sommet, atteignant
la dépression formée par le bourrelet apical; 3°, une strie semblable
a la précédente, déterminant avec elle un intervalle étroit, un peu
élevé vers Vextrémité; 4°, une strie ponctuée, fine, entiére, dé-
terminant avee la précédente un intervalle large, relevé en caréne
plus aeccentuée vers l’extrémité, atteignant le rebord apical; 5°,
une strie paralléle & la précédente, déterminant avec elle un inter-
valle étroit, faiblement écourtée au sommet, bordée vers lex-
trémité par une fine caréne; 6°, une strie humérale, finement
carénée, déterminant un intervalle large. Tarses plus longs que les
tibias.
| exemplaire.
Loc. ALDRABRA: Takamaka, xi. 1908 (Fryer).
CERYLINI.
CERYLON, Latreille, 1807, Gen. Crust. et Ins., IT, p. 205.
20. Cerylon nitidum, Grouvelle.
Cerylon nitidum, Grouvelle, 1896, Ann. Soc. Ent. France,
LXV, p. 85 et 86; 1906, LXXV, p. 114; (1908) 1909,
Rev. d’Ent. Caen, XXVII, p. 167.
Oblongum, convexum, nitidum, glabrum, castaneum; antennis
pedibusque dilutioribus. Antennae vix incrassatae; 2° articulo
sesquilongiore quam latiore, 9° clavam parante; clava oblonga,
subglandiformi. Caput transversum, convexum, antice trun-
catum, fronte in disco tenuiter, utrinque validius punctulatum. Pro-
thorax antice angustatus, lateribus antice arcuatus, postice paral-
lelus, modice transversus, in disco tenuissime, ad latera validius
punctulatus, punctis quam illis capitis majoribus; margine antico
subtruncato; lateribus pulvino et canaliculo concavo marginatis ;
basi medio retrorsum producta, ad extremitates tenuiter marginata.
Scutellum transversissimum, apice arcuatum. Elytra humeris
angulosa, vix dentata, lateribus arcuata, vix ampliata, apice fere
Coleoptera of the families Ostomidae, Monotomidae, ete. 31
conjunctim rotundata, paulo magis duplo longiora quam simul in
maxima latitudine latiora, tenuiter substriato-punctata; intervallis
planis, latis; punctis ad apicem et ad latera attenuatis; lateribus
stricte marginatis. Long. 2 mill.
Oblong, environ trois fois plus long que large dans sa plus grande
largeur, convexe, glabre, brillant, marron modérément fonce;
pattes et antennes plus claires. Antennes s’épaississant progressive -
ment 4 partir du 3™° article; 2™¢ environ une fois et demie plus
long que large, 8° peine plus long que large, 4° 4 8™° progressive-
ment un peu plus transversaux, 9° trés transversal, amorgant la
massue, 10™ oblong, environ une fois et demie plus long que large,
partagé en trois zones transversales : la premicre glabre, les deux
autres pubescentes. Téte moins de deux fois plus large que longue,
convexe, tronquée en avant, densément et plus fortement pointillé
sur les cétés que sur le disque; yeux saillants. Prothorax modeére-
ment transversal, subparalléle sur la majeure partie de sa longueur,
fortement arqué en dedans dans sa partie antérieure, presque lisse
sur le disque sauf a la base, progressivement plus fortement pointillé
de chaque cété vers les marges latérales, celles-ci fortement infléchies,
presque lisses; bord antérieur subtronqué, & peine sinué vers les
extrémités; angles antérieurs & peine marqués, arrondis; cOtés
bordés par un étroit bourrelet et par une fine goutti¢re limitée en
dedans par une ligne ponctuée; angles postérieurs presque droits,
émoussés; base trés faiblement arquée au milieu et subsinuée de
chaque c6té, bordée vers les extrémités par une ligne de petits
points. Ecusson environ trois fois plus large 4 la base que long,
trés largement arrondi. Elytres ovales, subdentés aux épaules, a
peine élargis sur les cOtés, présentant leur plus grande largeur vers le
premier quart de leur longeur, arrondis presqu’ ensemble au sommet,
un peu plus de deux fois plus longs que larges ensemble dans leur
plus grande largeur, finement ponctués-substriés; intervalles plans,
trés larges; stries ponctuées, atténuées vers le sommet et sur les
marges latérales; stries suturales & peine accentuées au sommet,
presqu’ effacées & la base; marges latérales fortement infléchies,
bordées par un étroit bourrelet, impressionnées 4 la base, contre la
bordure basilaire de Vélytre. Tibias postérieurs élargis progressive-
ment vers Vextrémité & partir du milieu de la longueur. Meéso-
sternum concave; métasternum ponctué sur les cdtés.
29 exemplaires.
Loc, SkycHELLES. Mahé: “ This species was found on
cultivated islets off Port Victoria, as well as at considerable
elevations in the main island of Mahé. Long Island, from
32 M. Antoine Grouvelle on
® felled coconut palm trunk, and Round Island, from
fungus, vii. 1908; also from the high forests of Morne
Blane and Pilot, and above Cascade Estate. Originally
discovered by Alluaud, 1892, in Mahé.”
21. Cerylon longius, n. sp.
Elongato-oblongum, convexum, nitidum, glabrum, castaneum;
antennis pedibusque dilutioribus. Antennae vix incrassatae; 2°
articulo vix sesquilongiore quam latiore, 9° clavam parante, clava
oblonga, subglandiformi. Caput transversum, subdepressum, antice
truncatum, vix perspicue punctulatum. Prothorax antice angu-
status, lateribus arcuatus, basin versus subparallelus, fere tam
elongatus quam basi latus, in disco tenuiter, ad latera validius,
parce punctulatus; margine antico utrinque sinuato; angulis
anticis obtusis, hebetatis; lateribus pulvino et canaliculo concavo,
ambobus strictis, marginatis; angulis posticis acutis, retrorsum
productis; basi medio arcuata, utrinque sinuata. Scutellum trans-
Versissimum, subpentagonale. Elytra humeris angulosa, lateribus
arcuata, Vix perspicue ampliata, apice conjunctim rotundata, magis
duplo longiora quam simul latiora, tenuiter substriato-punctata ;
intervallis planis, latis; striis punctatis ad apicem et ad latera
attenuatis; lateribus strictissime marginatis. Long. 1-4—-1°8 mill.
Oblong, plus de trois fois plus long que large dans sa plus grande
largeur, convexe, glabre, brillant, marron médiocrement foncé,
pattes et antennes plus claires. Antennes s’épaississant progres-
sivement a partir du 3™° article; 2™° environ une fois et demie
plus long que large, 3™° subégal au 2™°, 4™¢ subcarré, 4me A Sme
progressivement transversaux, 9™° transversal, 10™« suboblong,
moins d'une fois et demie plus long que large, partagé en trois zones
transversales : la premicre glabre, les deux autres pubescentes.
Téte moins de deux fois plus large que longue, subdéprimée, tronquée
en avant, 4 peine visiblement pointillée, yeux saillants. Prothorax
rétréci en avant, arqué sur les cétés, subparalléle contre la base,
presqu’aussi long que large 4 la base, couvert d’une ponctuation
éparse, fine sur le disque, un peu plus forte vers les marges latérales ;
celles-ci lisses, fortement déclives surtout vers le milieu; bord
antérieur arrondi en avant dans le- milieu, subsinué de chaque
coté; angles antérieurs obtus, émoussés; cdtés bordés par un
étroit bourrelet et par une trés étroite uttiére limitée en dedans
par une fine ligne ponctuée; angles postérieurs aigus, saillants en
arricre, base faiblement arquée en arriére dans le milieu, subsinuée
puis subarquée de chaque cdté, briévement rebordée vers les ex-
trémités. Ecusson subpentagonal, environ trois fois plus large
Coleoptera of the families Ostomidae, Monotomidae, etc. 33
que long. Elytres ovales, anguleux aux épaules, arrondis sur les
cotés, & peine élargis vers le premier sixi¢me de la longueur a partir
de la base, arrondis ensemble au sommet; nettement plus de deux
fois plus longs que larges ensemble dans leur plus grande largeur,
finement .ponctués-substriés; intervalles plans, trés larges; stries
ponctuées, atténuées vers le sommet et sur les marges latérales ;
stries suturales un peu accentuées au sommet, presqu’ eflacées a
la base; marges latérales fortement infléchies, bordées trés étroite-
ment surtout dans la partie apicale. Tibias postérieurs élargis dans
la partie apicale. Mésosternum concave; métasternum a peine
visiblement alutacé, ponctué sur les cotés. Dessous du corps en
partie pubescent.
15 exemplaires.
Loe. SEYCHELLES. Silhouette, Praslin: “ Silhouette,
several specimens from Mont Pot-a-eau, ca. 1500 feet;
also several from near Point Etienne, taken at the same
time and place as the series of Xuthia sicana and Lascotonus
scott? mentioned above. In Praslin seven specimens were
found in the forest of Coco-de-mer palms (Lodovcea), Cotes
d’Or Estate, x1. 1908.”
22. Cerylon perparvulum, n. sp.
Subparallelum, paulo magis ter longius quam latius, convexius-
culum, nitidulum, pilis erectis, tenuissimis parcissime vestitum,
dilute castaneum. Antennae subincrassatae; 2° articulo fere
sesquilongiore quam latiore, 3° longiore, 3°-9° paulatim parum
incrassatis, clava oblonga, subglandiformi. Caput transversum,
convexiusculum, antice subtruncatum, inter oculos arcuatim sub-
striatum; fronte vix perspicue punctulatum. Prothorax fere tam
antice quam postice latus, lateribus extra extremitates parallelus,
modice transversus, plus minusve parce punctulatus; margine
antico subtruncato; angulis anticis rotundatis; lateribus tenuiter
marginatis; angulis posticis obtusis; basi medio retrorsum arcuata,
utrinque vix perspicue sinuata. Scutellum subpentagonale, trans-
versum. Elytra humeris obtuse angulosa, lateribus arcuata, vix
ampliata, apice conjunctim rotundata, magis duplo longiora quam
simul in maxima latitudine latiora, punctato-striata; striis ad
latera attenuatis, apicem versus evanescentibus; intervallis in
disco quam punctis paulo latioribus, laeviter convexiusculis ; striis
suturalibus integris, apicem versus magis impressis; lateribus
strictissime marginatis. Long. 1 mill,
Subparalléle, un peu plus de trois fois plus long que large dans sa
plus grande largeur, faiblement convexe, un peu brillant, présentant
TRANS. ENT. SOC. LOND. 1918.—PARTS I, 11. (DEC.) D
A
34 M. Antoine Grouvelle on
sur son tégument des poils dressés, trés fins et relativement courts,
trés espacés, marron clair, antennes et pattes encore plus claires.
Antennes assez épaisses ; 1°" article dilaté-arrondi en dedans, presque
deux fois plus long que large, 2™° moins épais, presqu’une fois et
demie plus long que large, 3™° subcarré, 3™° a 9™° s’épaississant
progressivement, 4™° a 9™° transversaux, 10™° glandiforme, environ
une fois et demie plus long que large, et deux fois et demie plus large
que le précédent. 'Téte presque deux fois plus large au niveau des
yeux que longue. faiblement convexe, subtronquée en avant, coupée
entre les yeux par une faible impression arquée; partie avant cette
impression & peine visiblement ponctuée, partie en avant lisse,
infléchie au niveau des bases des antennes; marges latérales pro-
fondément sinuées en avant des yeux; ceux-ci médiocrement
saillants. Prothorax 4 peu prés aussi large en avant qu’en arri€ére,
subparalléle sur les cotés sauf vers les extrémités, qui sont briéve-
ment arquées, environ une fois et un quart plus large que jong,
couvert d'une ponctuation fine, irréguliérement éparse; bord
antérieur subtronqué; angles antérieurs arrondis; cotés bordés par
un fin bourrelet et par une étroite gouttiére ponctuée, lun et Pautre
briévement réfléchis contre la base; angles postérieurs obtus; base
arquée en arri€re, & peine subsinuée aux extrémités, bordée aux
extrémités, sur la partie réfléchie de la bordure latérale et au milieu,
par une ligne de petits points. Ecusson subpentagonal, environ
deux fois plus large que long. Elytres tronqués a la base, en angle
obtus aux épaules, arqués sur les cotés, 4 peine élargis, alors un peu
plus larges que le prothorax, arrondis ensemble au sommet, plus de
deux fois plus longs que larges ensemble dans leur plus grande
largeur, striés-ponctués; stries ponctuées atténuées sur les marges
latérales, effacées au sommet; stries suturales entiéres, fortement
enfoncées vers le sommet; intervalles légérement convexes, & peine
plus larges sur le disque, que les points; marges latérales arrondies,
puis verticales par rapport au plan de Vinsecte, masquant en partie
le bord latéral lorsque Vinsecte est vu de dessus, étroitement re-
bordées. Tibias postérieurs élargis dans la moitié apicale. Méso-
sternum incliné par rapport au plan du métasternum. Dessous
du corps éparsément pointillé.
22 exemplaires.
Loc. SEYCHELLES. Silhouette, Mahé, Praslin: “ In Sil-
houette five specimens were taken in the high forest near
Mont Pot-a-eau, ca. 1500 feet, one being recorded as from
a fallen and decayed trunk of ‘ Bois Rouge’ (Wormia
Jerruginea). In Mahé several were obtained in the most
elevated and dampest forests; Morne Blanc, Morne Sey-
Coleoptera of the families Ostomidae, Monotomidae, etc. 35
chellois, and Mare aux Cochons district. In Praslin eleven
were found in the Coco-de-mer palm forest, Cotes d’Or
Kstate.” ;
23. Cerylon tantillum, n. sp.
Elongato-oblongum, convexum, nitidum, pube flavo-cinerea,
brevi, tenui, erecta, in elytris inclinata, subdense vestitum, piceum ;
antennis pedibusque rufis. Antennae subincrassatae; 2° et 3°
articulo subaequalibus; clava glandiformi, sesquilongiore quam
latiore. Caput transversum, fronte convexiusculum et dense
punctulatum, ante antennarum bases arcuatim inflexum, antice
truncatum; oculis valde prominulis. Prothorax antice quam
postice paulo angustior, lateribus arcuatus, circiter | et } in maxima
latitudine latior quam longior, dense punctatus; margine antico
truncato; angulis anticis posticisque obtusis; lateribus pulvino et
canaliculo punctato stricte marginatis; basi subtruncata, ad ex-
tremitates marginata. Scutellum subpentagonale, transversis-
simum, punctulatum. Elytra basi quam prothorax paulo latiora,
humeris obtuse angulosa, lateribus arcuata, ampliata, apice separatim
breviter rotundata, circiter 1 et } longiora quam simul in maxima
latitudine latiora, vix perspicue rugosula, punctato-striata, punctis
et striis apicem versus attenuatis, his evanescentibus, illis minutis-
simis et confusis; striis suturalibus integris, ad apicem magis
impressis; intervallis plus minusve subconvexis, in disco quam
punctis latioribus, confuse tenuissimeque punctulatis. Pedes
robusti. Long. 1 mill.
Oblong, environ deux fois et deux tiers pius long que large dans
sa plus grande largeur, convexe, brillant, brun de poix avec les
antennes et les pattes rougedtres, couvert d’une pubescence flave-
cendrée, fine, dressée, courte, inclinée et plus dense sur les élytres,
leur donnant lorsque Vinsecte est frais un aspect un peu lanugi-
neux. Antennes un peu épaissies; 1° article épais, un peu plus long
que large, 2™° un peu épais, un peu plus long que large; 3™° subégal
au 2™°; articles 3™° a O™° s’épaississant faiblement et progressive-
ment, 4™¢ a 8™* transversaux, 9™° subcarré, 10™° glandiforme,
environ une fois et demie plus long que large, environ deux fois plus
large que le 9™*. Téte plus de deux fois plus large au niveau des
yeux que longue, trés finement et presque densément pointillée sur
le front, infléchie en arc en avant des naissances des antennes, sub-
tronquée au bord antérieur; bords latéraux paralléles en avant des
yeux, fortement sinués vers la base de Pantenne, trés convergents
en avant entre l’antenne et la base de la téte; yeux trés saillants,
coupés transversalement & leur bord antérieur. Prothorax un peu
36 M. Antoine Grouvelle on
plus rétréci en avant qu’a la base, arrondi sur les cétés, surtout dans
la partie basilaire, présentant sa plus grande largeur vers le premier
tiers de la longueur 4 partir te la base, environ une fois et un cin-
quiéme plus large dans sa plus grande largeur que long, densément
et assez fortement ponctué pour la taille; bord antérieur tronqué;
angles antérieurs et postérieurs obtus; cOtés étroitement bordés
par un bourrelet et un sillon, le dernier ponctué; base subtronquée,
bordée aux extrémités. Ecusson subpentagonal, trés transversal,
pointillé. Elytres 4 peine sinués 4 la base, en angle obtus aux
épaules, un peu plus large A la base que la base du prothorax, arqués
sur les cotés, assez nettement élargis, présentant leur plus grande
largeur vers le premier quart de la longueur 4 partir de la base,
séparément et briévement arrondis au sommet, ponctués-striés ;
stries et points atténués vers le sommet, les premiéres effacées avant
Vextrémité, les deuxiémes devenant trés fins et confus; intervalles
presque subrugueux, plus ou moins un peu convexes, plus larges sur
le disque que les points, éparsément, irréguliérement et trés fine-
ment pointillés; stries suturales entiéres, plus marqués au sommet ;
marges latérales arrondis, obliquement infléchies, bordées par une
fine strie 4 ponctuation écartée. Métasternum finement et peu
densément ponctué. Pattes robustes; tibias postérieurs s’élar-
gissant presqu’A partir de la base, arqués au bord externe. Cavités
des hanches antérieures presque fermées.
1 exemplaire.
Loc. SEYCHELLES. Mahé: ‘‘ From between leaf-bases of
a growing endemic palm (Stevensonia), near Morne Blane,
1908.”
24. Cerylon gardineri, n. sp. (PI. II, fig. 14.)
Elongate-oblongum, convexum, nitidum, pube flavo-cinerea,
tenui, subbrevi, praecipue in elytris dense vestitum, piceum; anten-
nis pedibusque rufis. Antennae subincrassatae; 2° articulo quam
3° paulo breviore; clava glandiformi, fere duplo longiore quam
latiore. Caput transversum, fronte subdense punctulatum, ante
antennarum bases angulose inflexum, antice truncatum; oculis
valde prominulis. Prothorax antice quam postice angustior,
lateribus arcuatus, fere 1 et } in maxima latitudine latior quam
longior, dense et quam caput validius punctulatus, punctis in disco
spatium laeve, strictum relinquentibus; margine antico truncato;
angulis anticis posticisque obtusis; lateribus basique marginatis, hac
truncata; marginibus lateralibus fere ad medium _ impressis.
Scutellum subpentagonale, transversissimum, parcissime punctula-
tum. Elytra basi quam prothorax paulo latiora, humeris sub-
a
Coleoptera of the families Ostomidae, Monotomidae, etc, 37
dentata, lateribus arcuata, vix ampliata, apice breviter conjunctim
rotundata, circiter 1 et 4 longiora quam in maxima latitudine
latiora, subaspera, punctatostriata; punctis ad basin sat validis,
apicem versus attenuatis et evanescentibus; striis suturalibus
sicut aliis impressis; intervallis quam punctis latioribus, tenuissime,
confuse et parce punctulatis. Pedes robusti. Metasternum dense
punctatum. Abdominis primum segmentum, ad latera, punctis
validis, densatis notatum. Long. 0°8—1°5 mill.
Oblong, environ deux fois et demie plus long que large dans sa
plus grande largeur, convexe, brillant, brun de poix avec les antennes
et pattes rougeatres, couvert d'une pubescense cendrée, un peu flave,
fine, dressée, inclinée et plus dense sur les élytres, donnant 4 Vinsecte
lorsqwil est frais un aspect en peu lanugineux. Antennes un peu
épaisses; 1 article épais, moins d'une fois et demie plus long que
large, légérement courbé; 2™° un peu épais, subcarré, 3™° environ
une fois et demie plus long que large, 4° a 8™° subégaux, plutdét
transversaux, sépaississant trés faiblement et progressivement,
gme suballongé, 10™* oblong, glandiforme, presque deux fois plus
long que large, un peu plus de deux fois plus large que le 9™*. Téte
plus de deux fois plus large au niveau des yeux que longue, presque
densément pointillée sur le front, infléchie en avant des naissances
des antennes en dessinant presque’un angle obtus, subtronquée au
bord antérieur; bords Jatéraux paralléles en avant des yeux, forte-
ment sinués vers la base de l’antenne, tres convergents en avant
entre l’antenne et la base de la téte; yeux trés saillants, coupés
transversalement a leur bord antérieur. Prothorax plus rétréci en
avant qu’a la base, arrondi sur les cotés, présentant sa plus grande
largeur vers le premier quart de la longueur a partir de la base, en-
viron une fois et demie plus large dans sa plus grande largeur que
long, présentant sur le disque un espace lisse, longitudinal, trés
étroit, ponctuation de chaque coté de cet espace serrée, plus forte que
celle de la téte, s’accentuant vers les bords latéraux; bord antérieur
tronqué; angles antérieurs et postérieurs obtus; cdtés bordés par
un bourrelet et une goutti¢re trés étroite; marges latérales impres-
sionnées vers le milieu de la longueur; base tronquée, bordée par
un étroit sillon. Ecusson subpentagonal, trés transversal et trés
éparsément pointillé. Elytres subsinués a la base en angle obtus,
subdentés aux épaules, un peu plus larges a la base que la base
du prothorax, arqués sur les cOtés, & peine élargis, briévement
arrondis ensemble au sommet, environ une fois et un tiers plus longs
que larges ensemble dans leur plus grande largeur, fortement ponc-
tués-striés; stries atténuées et effacées vers le sommet, atténuées
vers les bords latéraux ; intervalles subrugueux, trés finement, éparsé -
38 M. Antoine Grouvelle on
ment et irréguliérement ponctués; stries suturales marquées comme
les autres; bords latéraux trés fortement infléchis, finement
rebordés. Dessous de la téte, prosternum, mésosternum et méta-
sternum densément ponctués; 1% segment de l’abdomen encore
plus fortement ponctué, les autres en majeure partie lisses, présen-
tant une ligne ou une bande transversale de points, pubescents
surtout sur leur partie apicale.
Les exemplaires males ont en general les antennes plus longues
et moins épaisses, les premiers articles des tarses antérieurs’ plus
dilatés et les segments apicaux de abdomen plus mobiles.
Cette espéce, représentée par environ 265 exemplaires, est trés
variable comme taille, longueur des antennes caractérisée par la longu-
eur du 9™ article, rapport de la longueur totale a la largeur maxima,
largeur du prothorax par rapport a la largeur des élytres, force
et densité de la ponctuation, développement de la partie lisse du
prothorax, ete., ete.
Loc. SEYCHELLES. Silhouette, Mahé: “‘ Silhouette ; from
the high mountain forests, the majority of specimens
having “been found between bases of leaves of growing
endemic palms and Pandanus; there is a series of thirty- five
specimens from leaf-bases of two trees of Pandanus hornet
above Mare aux Cochons; a second series of seven specimens
from a Pandanus sechellarum in the same locality; a series
of thirteen specimens from a single Stevensonia palm also in
the same place; several other batches from Stevensonia leaf-
bases in other places; and a single immature example from
leaf-bases of the (in this respect unproductive) palm Ros-
cheria. In Mahé the species was found in several parts
of the mountain forests, and a few specimens are recorded
as from a low elevation, near the coast at Cascade. The
Mahé series includes ten examples from leaf-bases of a
Verschaffeltia palm, and one small and two large sets from
Slevensonia palms.”
25. Cerylon liliputanum, n. sp.
Oblongum, paulo magis ter longius quam latius, convexiusculum,
nitidum, pilis erectis, tenuissimis,: minutissimis, parcissime vesti-
tum, dilute castaneum. Antennae vix incrassatae; 2° articulo
paulo longiore quam latiore, cum 3° subaequali, 3°-9° paulatim
parum incrassatis, clava oblonga, glandiformi. Caput transversum,
convexiusculum, fronte vix perspicue punctulatum, ante antennarum
bases angulatim inflexum, antice truncatum. Prothorax antice
quam postice angustior, lateribus antice breyiter valde rotundatus,
Coleoptera of the families Ostonidae, Monotomidae, etc, 39
postice subrectus, retrorsum convergens, modice transversus, dense
punctatus; margine antico truncato; angulis anticis rotundatis ;
lateribus strictissime pulvinato-marginatis; angulis posticis obtusis,
basi subtruncata. Scutellum subpentagonale, transversum. Elytra
humeris obtuse angulosa, lateribus arcuata, parum ampliata, apice
conjunctim breviter rotundata, magis duplo longiora quam simul in
maxima latitudine latiora, punctato-striata, striis ad latera attenu-
atis, apicem versus evanescentibus ; intervallis in disco quam punctis
paulo latioribus, subplanis; striis suturalibus integris, apicem versus
fere magis impressis; lateribus stricte marginatis, Long. 0:8—0-9
mill,
Oblong, un peu plus de trois fois plus long que large dans sa plus
grande largeur, faiblement convexe, brillant, présentant sur son
tégument des poils dressés, trés fins, trés courts et trés espacés;
marron clair, antennes et pattes encore plus claires. Antennes a
peine €paissies; 1 article épais, dilaté-arrondi en dedans, un peu
plus long que large; 2° moins épais, subégal au 3™°, 3™° a 9™* s'épais-
sissant progressivement, 4™° 4 9™* serrés, transversaux, 10™° glandi-
forme, environ une fois et demie plus long que large et trois fois plus
large que le précédent. Téte plus de deux fois plus large au niveau
des yeux que longue, faiblement convexe, tronquée en avant, angu-
leusement infléchie en avant des bases des antennes, & peine visible-
ment pointillée; bords latéraux sinués en avant des yeux, ceux-cl
médiocrement saillants. Prothorax un peu plus rétréci en avant
qu’a la base, arrondi sur les cétés dans la partie antérieure, puis
droit, convergent vers l’arri¢re dans le reste de la longueur, environ
une fois et un quart plus large dans sa plus grande largeur que long,
densément et assez fortement ponctué pour sa taille; bord antérieur
subtronqué; angles antérieurs arrondis, cotés trés finement bordés
en bourrelet; angles postérieurs obtus; base faiblement arquée
en arriére. Elytres tronqués A la base, en angle obtus aux épaules,
arqués sur les cotés, un peu élargis, bri¢vement arrondis ensemble au
sommet, assez nettement plus larges dans leur plus grande largeur
que le prothorax et plus de deux fois plus longs que larges ensemble
dans cette plus grande largeur, striés-ponctués, stries atténuées sur
les marges latérales, effacées au sommet, stries suturales entiéres,
médiocrement enfoncées vers le sommet; intervalles presque plans,
& peine plus larges sur le disque que les points; marges latérales
arrondies, ne masquant pas le bord latéral lorsque linsecte est vu
de dessus, bordées par une strie bien marquée. Tibias postérieurs
élargis presque depuis la base. Mésosternum incliné par rapport
au plan du métasternum, cellui-ci assez densément et assez
fortement ponctueé.
AQ) M. Antoine Grouvelle on
2 exemplaires.
Loc. SEYCHELLLES. Mahé: ‘“ Mare aux Cochons dis-
trict, ca. 1500 feet, 1. 1909.”
26. Cerylon curtulum, n. sp.
Subovatum, postice attenuatum, sat valde convexum, nitidum,
glabrum, castaneum, antennis pedibusque dilutioribus. Antennae
sat incrassatae; 2° articulo subelongato, 3° clavam parante, clava
oblonga, crassa, subglandiformi. Caput transversum, ante anten-
narum bases vix productum, truncatum, inter oculos transversim
subplicatum. Prothorax antice valde, postice vix angustatus,
lateribus arcuatus, in maxima latitudine | et 4 latior quam longior,
in disco parce punctulatus, ad latera laevis; margine antico trun-
cato; angulis anticis obtusis; lateribus pulvino stricto et canali-
culo punctato, ambobus strictis, marginatis; angulis posticis subrec-
tis; basi medio subtruncata, ad extremitates retrorsum suboblique
truncata, marginata. Scutellum triangulare, minimum. Elytra
humeris obtuse angulosa, vix hebetata, lateribus arcuata, ampliata,
apice conjunctim breviter rotundata, circiter 1 et } longiora quam
simul in maxima latitudine latiora, substriato-punctata; punctis
sat validis, striis et punctis ad apicem et ad latera evanescentibus ;
lateribus strictissime marginatis. Long. 0°9—I-1 mill.
Oblong, environ deux fois et demie plus long que large dans sa
plus grande largeur, fortement convexe, glabre, brillant, marron peu
foncé; antennes et pattes plus claires. Antennes assez épaisses ;
le articule trés épais, dilaté-arrondi en dedans, environ aussi long
que large, 2™° médiocrement épaissi, 4 peine plus long que large,
3™e & peine épaissi, subégal au 2™*; 4™° a 9™* progressivement et
faiblement épaissis, 4™¢ A 8™e plus ou moins transversaux, serrés,
9me trés transversal, amorcant la massue; celle-ci oblique, aussi
longue que les articles 4"° & 9™* pris ensemble, environ une fois et
demie plus longue que large, terminée par une calotte pubescente.
Téte plus de deux fois plus large que longue, tronquée au bord anté-
rieur, convexe sur le front, transversalement subpliée entre les yeux,
& peine visiblement pointillée; bords latéraux transversalement
et bri¢vement tronqués en avant des yeux, fortement sinués pour
Vinsertion des antennes, trés fortement convergents en arriére
avant les yeux, ceux-ci petits, trés saillants, presque portés par un
pedoncule. Prothorax assez fortement rétréci en avant, faiblement
a la base, arrondi sur les cOtés, environ une fois et un tiers plus
large dans sa plus grande largeur que long, transversalement plus
convexe en avant qu’en arriére, éparsément et a peine visiblement
Coleoptera of the families Ostomidae, Monotomidae, etc. 41
pointillé vers les cotés; bord antérieur subtronqué; angles antéri-
eurs obtus; cdtés rebordés; angles postérieurs aigus, un peu sail-
lants en arriére; base subtronquée au milieu, obliquement réfléchie
en arri¢re de chaque coté, rebordée ; marges latérales et basilaires
trés bri¢vement et fortement infléchies contre la bordure marginale.
Ecusson triangulaire, plus. long que large. Elytres aussi larges
a la base que le prothorax, en angle obtus aux épaules, ne continu-
ant pas sur les cétés la courbure des cétés du prothorax, arrondis
sur les cdtés, un peu élargis, bri¢vement arrondis ensemble au
sommet, environ une fois ef un cinquiéme plus longs que larges en-
semble dans leur plus grande largeur, marqués de lignes substriées
de points assez forts, effacés sur les cétés et vers le sommet; inter-
valles des lignes assez larges; bords latéraux trés étroitement
rebordés. Convexité des élytres plutot forte. Pattes robustes.
Mésosternum infléchi par rapport au plan du métasternum, celui-ci
fortement, irréguli¢rement et épars¢ment ponctué sur les cétés.
_Epipleures relativement trés larges.*
87 exemplaires.
Loc. SEYCHELLES. Silhouette, Mahé: “Silhouette, a
few specimens from the mountain forests near Mont Pot-
a-eau and Mare aux Cochons, including seven from a fallen
and rotten trunk of an endemic palm, one from between
leaf-bases of a growing Roscheria palm, and one from a
fallen and rotten trunk of ‘ Bois Rouge’? (Wormia). In
Mahé the majority were found in the high forest of Morne
Blane, and a few in several other localities.”
AXIOCERYLON, nov. gen.
Antennae 9-articulatae; clava uniarticulata. Antennae in sulcis
prosternalibus receptae; clava in prosterni depressione basilari
recepta. Processus prosternalis latus, apice haud inflexus nec
* While making a preliminary sorting of the material previous
to sending it to Mons. Grouvelle, I removed the elytra of examples
of a number of forms in order to examine the condition of the meta-
thoracic wings. These were found to be normally developed in all
cases except three, namely Paralyreus scotti and Thyroderus sculpti-
collis (q. v.), and Cerylon curtulum. In the latter, six specimens were
examined, and in all of them the wings are minute vestiges of re-
markable form. They appear to be only about 1 the length of the
elytra, though exact measurement is difficult, and j in balsam prepara-
tions (two of which were made) they are hardly visible at all owing
to their transparency. They are extremely narrow in proportion
to their length, the basal part being almost handle- or thread-like,
while the distal part is only very little wider.—H. 8.
492 M. Antoine Grouvelle on
productus, obtuse acuminatus. Abdominis primum segmentum
elongatum, metasterno longius; segmentis aliis brevissimis.
Le genre Axzocerylon doit se placer prés du genre Glypto-
lopus, Kr.; il faut lui rapporter le Cautomus monstruosus,
Grouvelle (1 905, Bull. Soc. Ent. France, p. 109), de Sierra
Leone. Les deux espéces cavicolle et monstruosum sont
trés voisines; la premiére a les intervalles des carénes des
élytres confusément ponctuées, la deuxiéme est ponctuée
en lignes sur ces intervalles. Une troisiéme espéce encore
inédite, provenant de Sierra Leone, est encore plus voisine
de la forme des Seychelles; les intervalles des carénes de
ses ély tres sont également ponctués en lignes, mais cette
ponctuation est plus forte et les carénes ne s’accordent pas
avec celles de l’A. cavicolle.
27. Axiocerylon eavicolle,n. sp. (PI. IT, fig. 13.)
Breviter oblongum, convexissimum, nitidum, glabrum, atrum;
antennis pedibusque dilute piceis. Antennae subgraciles; 2° articulo
subincrassato, fere duplo longiore quam latiore; clava oblonga, tri-
bus partibus transversis divisa; 1* glabra, duabus aliis pubescentibus,
ultima apice acuminata. Caput modice transversum, inter anten-
narum bases angulatim vix carinatum, postice subdense, antice
dense punctatum ; margine antico arcuato. Prothorax transversus,
antice sat valde, postice vix attenuatus, antice margine abrupto laevi,
ad extremitates angulatim dilatato, praetextus; disco transversim
excavato, lateribus valde abrupteque inflexo; marginibus depressis,
latis, singulo duobus tuberculis elevatis instructo; intervallis inter
discum, tuberculos et margines laterales in maxima parte profunde
excavatis; tuberculo antico quadrilatero magno, cum margine
laterali per angulum externum juncto, postico elongato, obliquo-
subcarinato, extus juxta extremitatem basin attingente, intus
depressione lata ex disco separato; excavatione transversa antice
abrupta, postice obliqua; disco, ante excavationem dense, postice
subparce, punctato. Elytra tam elongata quam simul lata, apice
separatim obtusissime subacuminata, lineato-punctata; in singulo,
intervallo 2° modice, humerali valde carinatis; marginibus laterali-
bus valde inflexis, juxta latera valde punctatis et stricte concavo-
pulvinatis. Long. 1°5—1:7 mill.
Oblong, un peu moins d’une fois et demie plus long que large,
trés convexe, glabre, brillant, noir; antennes et pattes roux de poix
clair. Antennes assez gréles; 1 article épais, dilaté-arrondi en
dedans, a peine plus long que large; 2™° moins épais, environ
Coleoptera of the families Ostomidae, Monotomidae, etc. 43
deux fois plus long que large; 3™° un peu allongé, 4™° subcarré,
5me & 8me plus ou moins transversaux, 9™° formant une massue
oblongue, plus d'une fois et demie plus longue que large, partageée
en trois zones transversales : la premi¢re occupant environ la moitié
de la longueur, glabre, les deux autres pubescentes, la dernicre
acuminée. Téte infléchie, cachée dessous le pronotum, un peu
moins longue que large au niveau des yeux, anguleusement subpli¢e
entre les bases des antennes, trés densément ponctuée en avant de ce
pli, moins densément en arri¢re, longitudinalement subpliée sur le
front; épistome développé, arrondi en avant; bords latéraux sinués-
échanerés 4 Vinsertion des antennes. Yeux petits, trés saillants.
Prothorax fortement rétréci en avant, faiblement a la base, coupé
transversalement vers le 1° tiers de la longueur, & partir du sommet,
par une forte excavation, a profil anguleuse, striée au fond, profondé-
ment impressionnée aux extrémités, limitée en avant par une carcne
un peu arquée vers l’avant, en arriére par une caréne arquée vers
Varriére et de chaque c6té par un sillon longitudinal trés tourmente.
Bord antérieur apparent lorsque Vinsecte est vu de dessus, arqué,
bordé par une caréne; marge antérieure réelle, invisible de dessus,
normale au plan de Vinsecte, trés étroite au milieu, s’¢largissant vers
les extrémités, alors subconcave, formant en avant et en arricre des
angles aigus, bordée en avant et sur les cétés par un faible bourrelet.
Marge antérieure de l’excavation transversale presque brusquement
infléchie, postérieure assez longuement inclinée au milieu, la premicre
densément ponctuée, la deuxiéme ponctuée contre le bord supérieur ;
parties du disque comprises entre les sillons latéraux, Pexcavation
transversale, le bord antérieur apparent et la base, densément ponc-
tuées. Sillons latéraux plus ou moins profonds, formant de véritables
coupures normales au plan de lTinsecte, commengant en avant,
entre le bord latéral et l’extrémité de la marge infléchie du bord
antérieur, suivant le bord de la partie discoidale antérieure, alors
assez larges et assez profonds, fortement rétrécis devant Pexcavation
transversale par un lobe quadrangulaire, trés convexe, contigus au
bord latéral par un des sommets, puis longeant la partie discoidale
postérieure, alors larges et fortement impressionnés, bordés en
dehors par une forte saillie caréniforme un peu oblique, partant de
la base, atteignant presque le lobe quadrangulaire et séparés de lui
et des bords latéraux par des intervalles profonds; bords latéraux
terminés en bourrelet, ornés de deux petits tubercules entre le lobe
quadrangulaire et la base; celle-ci largement obtuse au milieu,
rebordée. Ecusson invisible. Elytres environ aussi longs que
larges ensemble, séparément et trés largement acuminés-emousses
au sommet, fortement ponctués en lignes, 4 peine striés; 2™° inter-
valle dorsal et intervalle huméral relevés: le 1° médiocrement,
44 M. Antoine Grouvelle on
le 2™° plus fortement, caréné, n’atteignant pas le sommet. Marges
latérales fortement infléchies, marquées de deux lignes de points,
la 2™¢ plus forte bordant le rebord latéral. Dessous a peine brillant,
trés finement chagriné, couvert d’une ponctuation grise, peu pro-
fonde, irréguliére, serrée sur le prosternum et les c6tés du méso-
sternum, trés espacée sur le milieu du premier segment de l’abdomen,
effacée sur les autres segments.
16 exemplaires.
Loc, SEYCHELLES. Silhouette, Mahé: ‘‘ Four specimens
were obtained in Silhouette, three from the much-decayed
fallen trunk of an endemic palm, and one between leaf-
bases of a growing Roscheria palm. In Mahé examples
were taken at high elevations in the forests of Morne Blane,
Morne Seychellois, and Cascade Estate.”
THYRODERUS, Sharp, 1885, Journ. Linn. Soc. Lond., Zool.,
XIX, p. 82.
28. Thyroderus sculpticollis, n. sp. (PI. IT, fig. 12.)
Oblongo-subparallelus, convexus, disco elytrorum subdepressus,
nitidus, glaber, castaneus, antennis pedibusque dilutior. Antennae
breves; clava subglobosa, glandiformi. Caput fronte convexius-
culum, crebre punctulatum, antice truncatum. Prothorax trans-
versus, antice modice, postice parum angustatus, paulo ante medium
transversim et utrinque plus minusve in longitudinem profunde
striato-impressus; lobo ante impressionem transversam convexo,
antice quam postice latiore, tenuiter denseque punctulato; lobo
postico latiore, in longitudinem modice trisulcato, tenuiter punctu-
lato; impressionibus lateralibus juxta basin lobi antici latioribus ;
marginibus lateralibus pulvinatis, ante sulcum transversum sub-
sinuatis. Elytra subparallela, ad apicem sinuata et breviter
conjunctim rotundata, circiter sesquilongiora quam latiora; singulo
in longitudinem quadri-carinato; 1* carina suturali vix elevata, 2*
et 3* dorsalibus et 4° laterali elevatis, integris, intervallis valde
bilineato-punctatis. Long. 0-7 mill.
Oblong, subparalléle, environ deux fois plus long que large dans
sa plus grande largeur, convexe, déprimé sur le disque des élytres,
glabre, brillant, marron; antennes et pattes plus claires. Antennes
courtes, épaisses; 1 article arrondi-dilaté en dedans, environ
aussi long que large, 2™* presqu’une fois et demie plus long que
large, 3™° a 7™° serrés, transversaux, progressivement atténués,
8™¢ formant une massue subglobuleuse, glandiforme, T¢te trans-
Coleoptera of the families Ostomidae, Monotomidae, etc. 45
versale, tronquée en avant, un peu convexe sur le front, trés
densément pointillée. Prothorax modérément rétréci en avant,
faiblement 4 la base, environ une fois et demie plus large dans sa
plus grande largeur que long, coupé transversalement, un peu avant
le milieu, par une impression sulciforme profonde, limitée de chaque
edté & un sillon longitudinal, ondulé, séparé du bord latéral par un
bourrelet plus ou moins étroit; bord antérieur arqué dans le milieu,
sinué de chaque cdté devant le sillon longitudinal; angles antérieurs
obtus, émoussés; cdtés biarqués, sinués devant limpression trans-
versale; angles postérieurs faiblement obtus; base anguleuse dans
le milieu, subsinuée de chaque cdté. Lobe (antérieur) compris entre
le bord antérieur et les sillons longitudinaux et le sillon transversal,
convexe, rétréci vers la base, finement et trés densément pointillé;
lobe (postérieur) compris entre la base, les sillons latéraux et le
sillon transversal, convexe, plus large en avant que le lobe antérieur,
rétréci vers la base, finement et densément pointillé, partagé en
avant en quatre lobes convexes par trois sillons longitudinaux, dont
lintermédiaire est mieux marqué; bourrelets marginaux dilatés
en dedans un peu en avant du sillon transversal et moins fortement
dans la partie basilaire; marge basilaire étroitement explanée,
densément pointillée. Ecusson caché. Elytres paralléles, a la base
de la largeur du prothorax, fortement sinués sur les cétés avant le
sommet et enfin briévement arrondis ensemble a Vextrémité;
chacun avec quatre carénes longitudinales; la premiécre suturale
peu marquée, la 2™ et la 3™° dorsales accentuées, entiéres, la
4me Jatérale et humeérale, également entiére. Intervalles entre ces
carénes avec deux lignes de points enfoncés. Métasternum et
sommet du premier segment de abdomen coupés par une impres-
sion longitudinale, peu marquée.*
2 exemplaires.
Loc. StycHeties. Silhouette, Mahé: “ Both — speci-
mens from high elevations, in the forests of Mont Pot-i-eau
(Silhouette) and Morne Blane (Mahé), respectively.”
Mycuocerus, Erichson, 1845, Naturg. Ins. Deutschl., II,
p. 292, note 4.
29. Mychocerus alluaudi, Grouvelle.
Mychocerus alluaudi Grouvelle, 1894, Ann. Soc. Ent.
France, LXIII, p. 15
* An elytron of Thyroderus sculpticollis became detached acci-
dentally, revealing the fact that the specimen has no apparent trace
of metathoracic wings [cf. Paralyreus scotti and Cerylon curtulum,
pp. 24, 41].—H. 8.
46 M. Antoine Grouvelle on
Oblongus, convexus, nitidus, glaber, castaneus; antennis pedibus
dilutioribus. Antennae sat incrassatae, 8-articulatae; 2° articulo
subelongato, quam 3° paulo longiore, 6° et 7° quam praecedentibus
paulo angustioribus; clava suboblonga, intus magis dilatata.
Caput transversum, antice truncatum, fronte convexiusculum.
Prothorax antice valde angustatus, lateribus arcuatus, juxta basin
antrorsum convergens, basi fere duplo latior quam longior; vix
perspicue punctulatus; margine antico subtruncato; angulis anticis
obtusis, vix indicatis; lateribus strictissime marginatis; angulis
posticis acutis; basi medio arcuatim producta, utrinque transversim
subtruncata, extra extremitates tenuissime punctato-marginata.
Scutellum transversum, subpentagonale. Elytra humeris angulosa,
lateribus arcuata, vix ampliata, apice conjunctim breviter rotundata,
circiter 1 et $ longiora quam simul in maxima latitudine latiora,
punctato-lineata, ex parte vix striata; punctis apicem versus et ad
latera evanescentibus; intervallis latis, planis. Long. 0°9-1:2 mill.
Oblong, environ deux fois plus long que large dans sa plus grande
largeur, convexe, glabre, brillant, marron peu foncé; antennes et
pattes plus claires. Antennes de 8 articles, assez épaisses; 1%
article épais, environ une fois et demie plus long que large, recourbé
dans la partie antérieure, 2" moins épais, subcarré, 3™° & 5™° plus
ou moins transversaux et subtransversaux, progressivement et trés
faiblement rétrécis, 6™¢ et 7™° transversaux, plus étroits que les
précédents, 8™° oblong, un peu moins d’une fois et demie plus long
que large, a peine moins long que les articles 3™° & 7™* réunis, un
peu plus dilaté en dedans qu’en dehors, terminé par une calotte
pubescente. Téte moins de deux fois plus large que longue, sail-
lante anguleusement en avant des naissances des antennes, -infléchie,
tronquée au bord antérieur, modérément convexe sur le front, a peine
visiblement pointillée; yeux modérément saillants. Prothorax
fortement rétréci en avant, faiblement arqué sur les cétés, ceux-ci
convergents en avant dés la base, presque deux fois plus large a la
base que long, & peine visiblement pointillé de chaque cété du disque,
principalement vers la région basilaire; bord antérieur subtronqué ;
angles antérieurs obtus, & peine marqués; cdtés bordés par un trés
fin bourrelet et par une trés étroite canelure ponctuée; angles pos-
térieurs aigus; base arrondie en arriére dans le milieu, tronquée
transversalement de chaque cdté, bordée sauf au milieu et aux
extrémités par une ligne de trés petits points. Ecusson subpen-
tagonal, environ deux fois plus large que long. Elytres en angle
un peu obtus aux épaules, continuant la courbure des cdtés du
prothorax, arqués sur les cétés, 4 peine élargis, bri¢vement arrondis
ensemble au sommet, environ une fois et demie plus longs que larges
Coleoptera of the families Ostomidae, Monotomidae, etc. 47
ensemble dans leur plus grande largeur, ponctués-substriés; points
assez forts vers la base, atténués puis effacés vers le sommet et
sur les marges latérales; celles-ci tres étroitement rebordées ; inter-
valles larges, plans, stries suturales effacées au sommet. Convexité
longitudinale des élytres continuant la convexité du prothorax.
Mésosternum se développant presque dans le plan du métasternum.
Strie marginale des hanches intermédiaires arquée, rejoignant leépi-
sterne un peu au dela du milieu de sa longueur, bordée en dehors par
une ligne de points; métasternum ponctué en dedans de la strie
marginale. Saillie du premier segment de LPabdomen entre les
hanches postérieures sinuée; strie marginale arquée en dedans,
rejoignant presque le bord latéral du segment, mais n’atteignant
pas son sommet.
48 exemplaires.
Loc. SeycuHeties. Silhouette, Mahé, Praslin, La Digue,
Félicité: ‘ Not confined to the mountain forests, but found
also in cultivated places and at low elevations. In Sil-
houette a number were obtained near the coast at Pointe
Etienne, under the bark of felled trees, with Xuthia sicana,
Lascotonus scotti, and Cerylon longius; others were taken
in the high mountain forests at 1000 feet and more, includ-
ing one from a rotting trunk of an endemic palm. In
Mahé examples were found at considerable elevations in
Cascade Estate and Morne Blane district. Two were also
obtained in the cultivated islet, Long Island, from a felled
coconut-palm trunk. Praslin: one specimen from Cotes
d’Or Estate. Félicité: two specimens. Originally dis-
covered by Alluaud, 1892, in Mahé and La Digue.”
TABLEAU DES CERYLINI DES SEYCHELLES.
1. Des fossettes antennaires surle prosternum. . . . . 2.
Pas de fossettes antennaires surle prosternum . . . . 4.
2. Fossettes antennaires contre le bord antérieur du proster-
num. Surface du prothorax sans impressions ou ex-
cavations (Mychocerus) .. . . . . «~~ .alluaudi, Grouy.
— Fossettes antennaires atteignant le bord postérieur du
prosternum. Surface du prothorax irrégulicre . . 3.
3. Sillons antennaires terminés par une fossette contre le bord
postérieur du prosternum (Axiocerylon) . . cavicolle, n. sp.
— Fossettes antennaires s’étendant entre les bords antérieurs
et postérieurs du prosternum (Thyroderus). sculpticollis, n. sp.
deomsecte glabre.-4 < (.98 3) Ge
— Insecte pubescent . .
or
. . .
~I
.
48 M. Antoine Grouvelle on
5. Premier segment de abdomen plus long que le métaster-
num. Cavités cotyloides ouvertes (Cerylon) curtulum, n. sp.
— Premier segment de ’abdomen au plus égal au métaster-
num; cavités cotyloides ouvertes . . . . . . . 6.
6. Stries des élytres également oe a la base, plus forte-
ment ponctuées . . “ts « « longius, nosp.
— Stries humérales plus fanenene marquées a la base, toutes
plus finement ponctuées . . . . . .nitidum, Grouy.
7. Elytres moins de deux fois plus longs que larges ensemble.
Pubescence plutdt longue, assez dense, sublanugineuse
gardineri, n. sp.
— Elytres au moins deux fois plus longs que larges ensemble.
Pubescence trés fine . .. . AO eae eee Th 8.
8. Ponctuation des élytres confuse vers ie sommet. Pro-
thorax nettement plus étroit en avant qu’a la base
tantillum, n. sp.
— Ponctuation des élytres réguliére. Prothorax 4 peu prés
aussi large en avant qu’a la base. . . . . . . Sh
9. Métasternum densément ponctué. Ponctuation des
élytres plus fine oe lee Selene eae LUlepurarii Aen sas
— Métasternum peu densément ponctué. Ponctuation des
élytres plus forte . . . . . . perparvulum, n. sp.
NOTIOPHYGIDAE.
Cing espéces représentent cette famille dans les collec-
tions rapportés par la Perey Sladen Trust Expedition ;
toutes appartiennent au genre Aphanocephalus, Wollaston,
genr représenté dans les parties tropicales et subtropicales
du monde entier. Pour le moment les A phanocephalus
semblent beaucoup plus nombreux dans les régions de
Yancien continent, mais les belles découvertes de la Perey
Sladen Trust Expedition montrent qu’on doit s’attendre
& voir le nombre des Aphanocephalus augmenter dans des
proportions considérables. La famille des Notiophygidae
(Notiophygus 1834, Discoloma 1845) comprend un ensemble
Wespéces remarquables par les pores distribués sur la téte
et les cotés du prothorax et des élytres. Le genre Disco-
genia, Kolbe (Deutsch. Ost-Afrika, IV, Kaf. 1898, p- 112)
ne semble pas & sa place parmi les Notiophygidae ; a mon
avis il doit étre rapproché des Trichopteryz.
APHANOCEPHALUS, Wollaston, 1873, Ent. Monthly Mag.,
XI, p. 278; Matthews, 1899, Monog. Coryloph., p. 19%,
Coleoptera of the families Ostomidae, Monotomidae, ete. 49
pl. 7, fig. ¢; Grouvelle, 1912, Notes Leyden Mus.,
XOEXTV: 7.197:
30. Aphanocephalus insularis, n. sp.
Breviter oblongus, convexus, nitidus, pilis flavo-cinereis, tenuibus,
dense vestitus, piceus, prothoracis elytrorumque marginibus stricte
rufus. Antennae subincrassatae. Caput transversum, antice late
arcuatum, inter antennarum bases tenuiter striatum, fronte tenuiter
punctulatum, epistomo sublaevi. Prothorax antice valde, postice
vix angustatus, basi fere ter latior quam longior, subparce tenuiter
punctulatus; punctis ad latera paulo validioribus; margine antico
truncato; angulis anticis rotundatis, tenuiter marginatis; lateribus
in maxima parte parum, juxta basin valde rotundatis, extra basin
sat late subconcavo-explanatis; angulis posticis subrectis; basi
ante scutellum truncata, utinque longe sinuata. Elytra oblonga,
paulo longiora quam simul latiora, punctis parum impressis, irregu-
lariter dispersis, notata; intervallis praecipue juxta suturam, dense
et saepe vix perspicue punctulatis; angulis humeralibus obtusis,
vix hebetatis; lateribus tenuiter pulvinato-marginatis et sat late
concavo-explanatis. Long. 1°2-1°5 mill.
Oblong, environ une fois et demie plus long que large, convexe,
brillant, couvert dune pubescence flave-cendrée, serrée, dressée,
brun de poix, marges latérales du prothorax et des élytres trés
étroitement rougeatres lorsque la coloration de l’insecte est compléte,
plus ou moins largement dans le cas contraire; antennes et pattes
brun clair. Antennes un peu épaisses; 1 article environ deux fois
plus long que large, 2™° subtransversal, 3™° environ une fcis et
demie plus long que large, 4™° et 5™° subcarrés, 5™* & 8™* un peu
moins épais que les précédents, subtransversaux; massue subob-
longue, nettement plus longue que large. Téte cachée par le pro-
thorax lorsque linsecte est vu de dessus & l'état normal, saillante
en avant des naissances des antennes en lobe subtronqué au sommet,
environ deux fois plus large que long, 4 peine visiblement poin-
tillé, transversalement convexe; strie interantennaire fine; front
densément et trés finement pointillé. Prothorax fortement rétréci
en avant, 4 peine 4 la base, presque trois fois plus large dans
sa plus grande largeur que long, subépars¢ément et finement
pointillé de points un peu plus forts vers les marges latérales ;
bord antérieur tronqué; angles antérieurs arrondis, finement re-
bordés; cdtés faiblement arrondis sur la majeure partie de leur
longueur, fortement contre la base, bordés par un fin bourrelet et
par une explanation subconcave assez large, natteignant pas la
base; angles postérieurs driots; base, tronquée devant lécusson,
TRANS. ENT. SOC. LOND. 1918.—PARTS I, H. (DEC.) E
50 M. Antoine Grouvelle on
longuement sinuée de chaque cdté. Ecusson triangulaire, moins
large 4 la base que long, & peine pointillé. Elytres oblongs, un
peu plus plongs que larges dans leur plus grande largeur, ponctués
de points peu enfoncés, irréguli¢rement dispersés, séparés par des
intervalles & peine visiblement pointillés, sauf contre la suture;
base trés finement rebordée; angles huméraux obtus, un peu
émousses ; bords latéraux, bordés par un bourrelet et par une explana-
tion concave, assez large, séparée du disque par des points irrégu-
licrement espacés. Métasternum presque lisse sur le disque, sub-
éparsément ponctué sur les cdtés; 1° segment de abdomen éparsé-
ment ponctué sur le disque, plus densément et* plus fortement sur
les cétés.
93 exemplaires.
Loc. SEYCHELLES. Silhouette, Mahé, Praslin: ‘‘ From
the endemic mountain forests. Silhouette, near Mont Pot-
a-eau and above Mare aux Cochons, including four speci-
mens from leaf-bases of a growing Slevensonia palm. Mahé;
near Morne Blanc, above Cascade Estate, ete., including
two specimens from leaf-bases of a growing Slevensonia
in the stunted forests on the summit of Mount Sebert.
Praslin; a considerable series from the Coco-de-mer forest
in the Vallée de Mai, Cotes d’Or Estate, xi. 1908.” Cette
espéce a été aussi récoltée a Vile Maurice par M. Carié.
31. Aphanocephalus binotatus, n. sp. (PI. I, fig. 4.)
Breviter oblongus, convexus, nitidus, tenuissime, dense, flavo-
cinereo-pubescens, ater; prothoracis marginibus anticis laterali-
busque, in singulo elytro plaga oblonga, transversa, paulo ante
medium posita, elytrorum marginibus reflexis, antennis pedibusque
fulvis. Antennae vix incrassatae, Caput transversum, antice
truncatum, inter antennarum bases striatum; epistomo transversim
sat convexo; labro sat producto. Prothorax antice valde, postice
modicissime angustatus, lateribus praecipue ad basin rotundatus,
in maxima latitudine circiter ter latior quam longior, dense tenui-
terque punctulatus, margine antico truncato, extra medium tenuiter
marginato; angulis anticis rotundatis, tenuiter marginatis; lateri-
bus pulvino tenui et margine reflexo, praecipue in medio dilatato,
basin haud attingente, marginatis; angulis posticis parum obtusis;
basi ante scutellum truncata, utrinque praecipue ad extremitatem
sinuata. Scutellum subtriangulare, transversum, tenuissime punce-
tulatum, in longitudinem subelevatum. Elytra oblonga, apice con-
junctim breviter rotundata, 1 et } longiora quam simul in maxima
Coleoptera of the families Ostomidae, Monotomidae, etc. 51
latitudine latiora, crebre tenuiterque punctulata, punctis plus
minusve sparsis vel densatis intermixtis; lateribus pulvino sub-
stricto et canaliculo concavo marginatis, pulvino sexies dilatato et
punctato. Long. 2 mill.
Oblong, environ une fois et deux tiers plus long que large dans
sa plus grande largeur, convexe, brillant, couvert @une pubescence
flave-cendrée fine, courte et serrée; noir, marges antérieures et
latérales du prothorax largement, antennes, pattes, marges réfléchies
des élytres et sur chacun d’eux une tache oblongue, transversale,
placée avant le milieu, roux. Antennes peu épaissies; 1% article
environ une fois et demie plus long que large, 2™° subcarré, 3™°
environ trois fois plus long que large, 4™° un peu allongé, 5™° & 8me
progressivement et faiblement plus épais, 5™° subcarré, G™e a 8me
subtransversaux, massue piriforme, presque deux fois aussi longue
que large. Téte presque cachée, lorsque Vinsecte est vu de dessus,
saillante en avant des naissances des antennes en forme de lobe
tronqué en avant, transversalement convexe, environ deux fois
plus large que long, séparé du front par une fine strie, & peine poin-
tillé; front plus densément pointillé; labre médiocrement saillant.
Prothorax trés rétréci en avant, trés faiblement a la base, arqué
sur les cdtés, fortement arrondi dans la partie basilaire, environ
trois fois plus large dans sa plus grande largeur que long, couvert
d'une ponctuation trés fine et serrée; bord antérieur subtronqué
lorsque Vinsecte est vu de dessus, trés finement rebordé sauf au
milieu; angles antérieurs arrondis, finement rebordés; cdtés bordés
par un fin bourrelet et par une marge explanée, large, surtout au
milieu, subconcave, n’atteignant pas la base; angles postérieurs
un peu obtus; base tronquée devant l’écusson, largement sinuée
de chaque c6té surtout vers lextrémité. Ecusson triangulaire,
moins de deux fois plus large a la base que long, trés finement
pointillé, longitudinalement et faiblement plié. Elytres oblongs,
arrondis aux épaules, alors trés nettement plus larges que le pro-
thorax dans sa plus grande largeur, arrondis sur les cOtés, assez
briévement arrondis ensemble au sommet, environ une fois et un
quart plus longs que larges dans leur plus grande largeur, couverts
d'une ponctuation serrée, trés fine, entremélée de points plus ou moins
forts et plus ou moins espacés ou serrés, effacés vers le sommet.
Marges latérales bordés par par un bourrelet relativement épais et
par une marge concave, médiocrement étroite; bourrelet présen-
tant en dedans six renflements ponctués, peu allongés. Métaster-
num plis densément mais moins fortement ponctué au milieu que
sur les cotés. 1° segment de abdomen densément ponctué comme
le milieu du métasternum.
52 M. Antoine Grouvelle on
2 exemplaires.
Loc. SEYCHELLES. Mahé: ‘ Caseade Estate, 800-1000
feet.”
32. Aphanocephalus quadriplagiatus, n. sp. (PI. IT, fig. 10.)
Oblongus, convexus, nitidus, pilis cinereis, brevibus, inclinatis
subdense vestitus, ater; antennarum basi tarsisque fulvo-testaceis ;
pedibus colore paulo nubilis ; singulo elytro duabus maculis flammeo-
testacis, latis ornato. Antennae parum incrassatae. Caput trans-
versum, antice truncatum, inter antennarum bases vix perspicue
striatum; epistomo transversim convexo; labro minimo. Pro-
thorax antice valde angustatus, lateribus parum arcuatus, circiter
basi ter latior quam longior, dense tenuiterque punctulatus, punctis
apicem versus attenuatis ; margine antico truncato, tenuissime margi-
nato; angulis anticis rotundatis, marginatis; lateribus pulvino
tenuissimo et margine concavo, stricto, juxta basin attenuato mar-
ginatis, angulis posticis acutis; basi ante scutellum sinuata et
utrinque praecipue ad extremitatem sinuata. Scutellum subtri-
angulare, tam longum quam basi latum. LElytra oblonga, apice
conjunctim rotundata, 1 et 2 longiora quam simul in maxima latitu-
dine latiora, tenuiter et plus minusve dense punctulata, punctis
majoribus irregulariter intermixtis; lateribus pulvino tenuissimo
et canaliculo concavo, stricto marginatis, pulvino quater dilatato
et punctato. Long. 1-4-1°6 mill.
Oblong, environ deux fois plus long que large dans sa plus grande
largeur, convexe, brillant, couvert d’une pubescence cendrée, courte,
inclinée, assez dense, noir; base des antennes roux de poix clair,
fémurs et tibias plus ou moins plus foncés; sur chaque élytre deux
larges taches roux orangé, la postérieure atteignant presque la
suture et le bord latéral. Antennes peu épaissies; 1° article environ
une fois et demie plus long que large, 2™* subcarré, 3™° environ
trois fois plus long que large, 4™° subcarré, 5™° & 8™° s’épaississant
progressivement et faiblement, transversaux, massue piriforme,
environ une fois et demie plus longue que large. Téte presque
complétement cachée lorsque Vinsecte est vu de dessus, saillante
en avant des naissances des antennes, en forme de lobe tronqué en
avant, transversalement convexe, plus de deux fois plus large que
long, séparé du front par une strie peu visible, 4 peine visiblement
pointillé; front un peu plus fortement pointillé; labre petit. Pro-
thorax fortement rétréci en avant, arrondi aux angles antérieurs,
faiblement arqué sur les cétés, environ trois fois plus large a la base
que long, couvert d’une ponctuation fine et serrée sur la région
Coleoptera of the families Ostomidae, Monotomidae, etc. 53
basilaire, plus ou moins effacée sur le reste de la surface; bord anteé-
rieur subtronqué lorsque Vinsecte est vu de dessus, trés finement
rebordé; cotés bordés par un tres fin bourrelet et par une étroite
marge concave, atténuée a la base; angles postérieurs aigus; base
tronquée devant l’écusson, largement sinuée de chaque cété surtout
vers Pextrémité. Ecusson triangulaire, aussi long que large a la
base, trés finement pointille. Elytres oblongs, @ peine plus larges
dla base que la base du prothorax, arqués sur les cétés, trés faible-
ment élargis, arrondis ensemble au sommet, environ une fois et deux
cinquiémes aussi longs que larges ensemble’ dans leur plus grande
largeur, couverts dune ponctuation fine et serrée sur la région
suturale-discoidale, plus ou moins effacée sur le reste de la surface,
entremélée de points plus forts, irréguliérement dispers¢s. Bords
latéraux bordés par un bourrelet tres fin et par une marge concave,
étroite, effacée au sommet, limitée en dedans par une ligne de
points; bourrelet présentant en dedans quatre renflements marqués
d'un point. Métasternum irréguliérement et peu densément ponctue ;
1e* segment de abdomen ponctué & peu prés de meme.
Environ 40 exemplaires.
Loc. SEYCHELLES. Mahé: “ From near Morne Blanc,
and from Cascade Estate, 800-1000 feet.”
33. Aphanocephalus subdepressus, l). Sp. CRT, 1y 218 220%)
Breviter oblongus, modice conveXxus, elytrorum disco subde-
pressus, nitidus, pilis flavo-cinereis, tenuissimis, inclinatis dense
vestitus, brunneus ; antennis, prothoracis elytrorumque marginibus
reflexis, dilutioribus, pedibus dilute subpiceo-testaceis. Antennae sat
incrassatae. Caput transversum, antice sinuatum, inter antennarum
bases transversim subimpressum ; epistomo vix perspicue punctato.
Prothorax antice valde angustatus, postice breviter parallelus,
lateribus arcuatus, circiter basi 2 et 4 latior quam longior, dense
tenuiterque punctulatus ; margine antico subemarginato; angulis
anticis late obtusis, hebetatis ; marginibus lateralibus late expla-
nato-concavis, juxta apicem breviter reflexis; angulis posticis sub-
rectis; basi medio retrorsum producta, truncata, utrinque late
sinuata. Scutellum rufo-brunneum, triangulare, tam elongatum
quam basi latum. Elytra oblonga, lateribus arcuata, sat ampliata,
apice vix conjunctim rotundata, circiter 1 et } longiora quam simul
in maxima latitudine latiora, tenuiter et irregularissime punctu-
lata, punctis majoribus, irregularibus, praecipue ad latera validi-
oribus, intermixtis et irregulariter dispersis ; lateribus pulvino et
54. M. Antoine Grouvelle on
margine concavo sat lato marginatis; pulvino apicem versus
attenuato, pluribus punctis notato et juxta haec puncta vix
incrassato. Long. 1°5-1°7 mill.
Oblong, environ une fois et deux tiers plus long que large dans
sa plus grande largeur, modérément convexe, subdéprimé sur le
disque des élytres, brillant, couvert d’une pubescence flave-cendrée,
courte, inclinée et serrée, brun; antennes, marges réfléchies du
prothorax et des élytres plus claires, pattes testacé-claires, trés
légérement teintées de brun. Antennes assez épaisses; 1 article
environ une fois et demie plus long que large, 2™° subcarré, 3™¢
deux fois plus long que large, 4° & 8™° progressivement et & peine
visiblement épaissis, 4™° et 5™° subcarrés, 6™e A Sme plus ou moins
transversaux; massue piriforme, moins dune fois et demie plus
longue que large. T'éte presque cachée par le prothorax lorsque
Vinsecte est vu de dessus, saillante en avant des bases des antennes
en lobe sinué au bord antérieur, transversalement convexe, plus
de deux fois plus large que long, 4 peine visiblement pointillé; front
caché sous le prothorax, séparé de l’épistome par une impression peu
accentuée; labre petit. Prothorax fortement rétréci en avant,
briévement paralléle a la base, arrondi sur les cétés, environ deux
fois et demie plus large a la base que long, densément et finement
pointillé de points un peu plus forts de chaque c6té vers la base ;
bord antérieur subsinué; angles antérieurs trés largement obtus,
émoussés ; cOtés bordés par un trés fin bourrelet et par une marge
concave assez large, atténuée un peu avant la base, briévement ré-
fléchie contre le bord antérieur, marquée d’un point enfoncé contre
cet angle et @un autre point contre le bourrelet latéral vers le premier
conquicme de la longueur a partir de la base; angles postérieurs
presque droits; base saillante en arricre au milieu, tronquée devant
Pécusson, largement sinuée de chaque cété. Ecusson rougeatre, trian-
gulaire, aussi long que large a la base, presque lisse. Elytres oblongs,
arrondis sur les cétés, un peu élargis, arrondis presqu’ ensemble au
sommet, environ une fois et un cinquieme plus longs que larges
ensemble dans leur plus grande largeur, couverts d’une ponctuation
trés fine, plus ou moins visible, irréguliérement serrée, entremélée
de points trés irrégulicrement dispersés, en général plus forts et plus
serrés yers les cétés. Base trés finement rebordée vers les extrémités,
en angle obtus, un peu émoussé aux extrémités. COotés bordés par un
hourrelet assez marqué a la base, atténué vers le sommet et par une
marge concave assez large, atténuée également vers le sommet,
séparée de la convexité des élytres par une strie ponctuée peu régu-
liére; bourrelet présentant quelques points, ceux-ci n’entrainant
pas un épaississement sensible de son bord. Métasternum presque
Coleoptera of the families Ostomidae, Monotomidae, ete. 55
lisse au milieu, ponctué sur les cOtés; Le segment de Pabdomen
moins fortement ponctué au milieu que sur les cOtés,
9 exemplaires.
Joc. SEYCHELLES. Praslin: “The specimens were all taken
from between the leaf-bases of a single growing Coco-de-mer
palm (Lodotcea sechellarum) in the Vallée de Mai, Cotes
d’Or Estate, xi. 1908.”
34, Aphanocephalus acuminatus, n. sp.
Ovatus, apice attenuatus, convexus, nitidus, pilis cinereis, subla-
nuginosis subparce vestitus; piceus, antennis et prothoracis margi-
nibus lateralibus stricte ad angulos anticos fusco-testaceis; pedibus
dilutioribus. Antennae sat incrassatae. Caput fere tam elongatum
~ quam ad oculos latum, antice subsinuatum, inter antennarum bases
tenuiter striatum, fronte subasperum; epistomo sublaevi; labro
magno. Prothorax antice valde angustatus, lateribus arcuatus,
juxta basin antrorsum valde convergens, circiter basi ter latior quam
Jongior, dense tenuissimeque punctulatus, punctis juxta basin paulo
validioribus; margine antico subsinuato; angulis anticis rotun-
datis; lateribus pulvino tenui et margine concavo, modice lato, ante
basin evanescente marginatis; angulis posticis subrectis ; basi medio
arcuata, utrinque late sinuata, juxta extremitates leviter impressa.
Scutellum triangulare, basi latius quam longius, tenuissime punctu-
latum. Elytra oblonga, lateribus arcuata, vix ampliata, apice con-
junctim rotundata, fere tam longiora quam simul in maxima latitu-
dine latiora, plus minusve dense punctulata, punctis plus minusve
majoribus, irregulariter dispersis, intermixtis; lateribus pulvino
stricto et canaliculo substricto, ambobus ad apicem attenuatis,
marginatis. Long. 1°3-1-7 mill. °
Ovale, atténué en avant, un peu moins (une fois et demie plus
Jong que large dans sa plus grande largeur, brillant, couvert dune
pubescence cendrée, sublanugineuse, peu serrée, brun de poix avec
les antennes et une étroite marge vers les angles antérieurs du pro-
thorax testacées, enfumées; pattes plus claires. Antennes assez
épaisses; 1 article environ deux fois plus long que large, 2™° sub-
carré, 8™° moins d’une foiset demie plus long que large, 4™°-6™¢ plus
ou moins subcarrés 7™° et 8™° transversaux, massue subpiriforme,
environ une fois et un tiers plus longue que large. Téte un peu
moins longue que large au niyeau des yeux, en partie visible lorsque
Vinsecte est vu de dessus, saillante en avant des bases des antennes
en lobe subsinué au bord antérieur, subdéprimé a la base, progressive-
ment conyexe vers lavant, plus de deux fois plus large que long,
56 M. Antoine Grouvelle on
presque lisse; intervalle entre les bases des antennes finement strié,
impressionné au milieu; front trés finement pointillé, subrugueux ;
labre grand. Prothorax tres fortement rétréci en avant, arqué
sur les cétés, convergent vers Pavant contre les angles postérieurs,
environ trois fois plus large a la base que long, densément et trés
finement ponctué de points plus forts sur la région basilaire; bord
antérieur subsinué; angles antérieurs arrondis; cdtés bordés par
un fin bourrelet et par une marge concave, effacée avant la base ;
angles postérieurs aigus, un peu émoussés; base arquée en arricre
dans le milieu, largement sinuée de chaque cdté, impressionnée de
chaque cdté vers Vextrémité. Ecusson triangulaire, moins long que
large a la base, trés finement pointillé. Klytres oblongs, arqués
sur les cétés, un peu plus larges dans leur plus grande largeur
que le prothorax & la base, arrondis ensemble au sommet, environ
aussi longs que larges dans leur plus grande largeur, couverts’
dune ponctuation fine, plus ou moins dense, entremélée de points
plus forts, devenant encore plus forts vers les marges latérales,
irrégulicrement espacés; angles huméraux obtus, émoussés; cdtés
bordés par un bourrelet étroit et par une marge concave presqw
étroite, tous deux atténués vers le sommet; marge concave limitée
en dedans par une ligne de gros points irrégulicrement espacés ;
bourrelet présentant plusieurs points enfoncés ne Vépaisissant pas
sensiblement. Métasternum et 1* segment de labdomen presque
lisses sur le milieu, assez fortement et peu densement ponctués sur
les cOtés.
4 exemplaires.
Loc, SEYCHELLES. Silhouette, Mahé: “ From the high
mountain forests.”
TABLEAU DES APHANOCEPHALUS DES SEYCHELLES.
1. Prothorax rétréci ala base; une tache roux-testacée sur la
moitié basilaire de chaque élytre ; pubescence trés courte,
tresifine, serree a % s= 6) ue) sp) Ways UMoldiue mn. sp.
— Prothorax non rétréci dla base . . ... =... a2
2. Noir avec deux taches rouges sur chaque élytre ; pubescence
fine, sublanugineuse ; forme ovale, au moins deux fois
aussi longue que large . . . . quadriplagiatus, n. sp.
— Brun de poix, sans taches rouges . . . «1 « =» «+ Je:
3. Prothorax nettement tronqué au bord antérieur; pubes-
cence fine, courte et serrée; forme ovale, environ une
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SNEES ERD
N
Andre, Sleigh & Anglo, Ltd
COLEOPTERA FROM THE SEYCHELLES AND
ALDABRA ISLANDS.
Peo
SDS
EXPLANATION OF PratE I.
Bothrideres fryert, sp. NOV.
Tyrtaeus singularis, sp. Nov.
Lascotonus scotti, sp. nov.
Aphanocephalus binotatus, sp. Nov.
Aphanocephalus subdepressus, sp. NOV.
Ditoma cavicollis, sp. nov.
Sarothrias eximius, gen. et sp. NOV.
Colobicones singularis, gen. et sp. Nov.
EXPLANATION OF Puate II.
9. Cicones scotti, sp. nov.
10. Aphanocephalus quadriplagiatus, sp. nov.
11. Diplotoma capito, sp. nov.
12. Thyroderus sculpticollis, sp. nov.
13. Awiocerylon cavicolle, gen. et sp. nov.
14. Cerylon gardineri, sp. nov.
15. Paralyreus scotti, gen. et sp. nov.
16. Cicones compactus, sp. Nov.
[Note.—In figures 4, 11, 12, 16, certain of the appendages are
represented by dotted lines. The specimens are not defective,
but the appendages are bent beneath them and invisible from above ;
and the insects being very hard to relax, and in three of the cases
unique, did not admit of the manipulation necessary to spread the
appendages out.
It is almost impossible to represent adequately the remarkable
depth of the cavities on the thorax in figs. 12 and 13.—H. 8.]
Lond., 1918, Pl. II.
Soc.
nt.
E
Trans.
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AND
YCHELLES
ALDABRA ISLANDS.
4
RA FROM THE SEI
4
COLEOPTE
Coleopiera of the families Ostomidae, Monotomidae. ete. 57
— Prothorax arrondi au bord antérieur; élytres environ
aussi longs que larges 5, i a ee ee
4. Angles huméraux des élytres arrondis; forme oblongue,
environ une fois et demie plus longue que large, bien
arrondie en avant; pubescence assez longue, serrée ;
disque des élytres éparsément ponctué; écusson grand
insularis, n. Sp.
— Angles huméraux des élytres obtus, & peine émoussés ;
forme oblongue, un peu moins d'une fois et demie aussi
longue que large, subacuminée en avant; pubescence
plutot Jongue, sublanugineuse; écusson petit
acuminalus, nN. sp.
Ces cinq espéces ont les angles antérieurs du prothorax
aigus, la ponctuation des élytres plus ou moins espacée, le
tégument sans reflet métallique, pubescent; elles rentrent
dans le groupe 9 du tableau publié dans les Notes from the
Leyden Museum, XXXIV, 1912, p. 221. A. subdepressus
a les angles postérieurs du prothorax un peu saillants en
arriére; A. imsularis et acuminatus ne présentent pas ce
caractere.
EXPLANATION OF Puiatss I, II.
[See Explanation facing the PLATES. ]
II. New species of Staphylinidae from Singapore. Part I.
By Matcoitm Cameron, M.B., R.N., F.E.S.
[Read December 5th, 1917.]
Tuts paper contains descriptions of Staphylinidae collected
by myself in the Island of Singapore, between September
22nd, 1915, and December 20th, 1916. During this period
practically every part was visited, but owing to the -
very limited time at my disposal it cannot be. expected
that a complete collection has been made; indeed, there
are several species recorded which were not met with by
me. J may say, however, that I devoted myself entirely
to the collection of Staphylinidae, and 257 species were taken,
of which no fewer than 146 appear to be undescribed.
It is hoped that the paper will be concluded by synoptic
tables of all the species known in the island, which from its
position forms a link with India on the one hand and
the Malay Archipelago on the other. The ever-increasing
number of descriptions and the almost entire absence of
local “ Faunas ” dealing with this group is of course due to
the want of material, and this paper should help as a small
contribution to such local knowledge. The types of the
species described are all contained in my own collection.
The groups here dealt with are the Lispini, Oxyteli, Osorii,
Stenini, Pmophili, Paederini, Xantholinini, Staphylinini,
and Quediini.
LISPINt.
1. Aneaeus singularis, n. sp.
Linear, parallel, pitchy-brown, shining; head on either side of
front with a rounded impression; antennae and legs testaceous,
the former with 5-jointed club. Length 1°5-1°75 mm.
Somewhat resembling in facies the genus Lispinus. Smaller,
narrower and less shining than A.exiguus, Er., and of different appear-
ance due to the much longer head and thorax and less depressed
form. Head as long as broad; eyes somewhat prominent; temples
rather long, parallel, longer than the diameter of the eyes viewed
from above ; front truncate, with a rounded impression on each side ;
impunctate, but with a fine longitudinal strigose ground-sculpture.
TRANS. ENT. SOC, LOND. 1918.—PaRTS I, II, (DEC.)
Dr, Malcolm Cameron on Slaphylinidae from Singapore. 59
Antennae formed as in A. exiguus, the Ist joint stout, the 3rd
shorter than the 2nd, scarcely longer than broad, 4th, 5th and 6th
small and transverse, 7th to 10th considerably broader forming with
the last a distinct club. Thorax as wide as the head (including the
eyes), a little broader (at the anterior margin) than long, the sides
converging gradually backwards to a little before the posterior
angles, where they are slightly constricted; posterior angles bluntly
rectangular with distinct rounded impression adjacent; disc with a
fine median sulcus not nearly extending to the anterior or posterior
borders, and an obscure rounded impression on either side; anterior
margin with a minute fovea on either side nearer to the middle line
than to the anterior angles; sculpture as on the head, no visible
puncturation. Elytra as wide as the thorax at the anterior angles,
longer than broad, parallel, sutural stria distinct; disc with an
obscure fovea on either side; sculpture as on fore-parts, with the
addition of a few exceedingly fine, scarcely visible punctures.
Abdomen cylindrical, last segment testaceous, finely coriaceous,
each segment with a puncture on either side bearing an erect seta,
lateral setae feeble.
Hab. Bukit Panjang and Bukit Timah, under bark.
2. Lispinus setosus, n. sp.
Rufous, shining, head and abdomen pitchy; thorax transverse,
scarcely constricted at the base. Length 2°9 mm.
A rather brightly-coloured, shining species. Allied to L. impressi-
collis, Kr., and specularis, Bernh., but larger, and more robust and
shining, than the former, with the thorax scarcely constricted before
the base, both the median and lateral impressions less marked and
the setae everywhere more numerous and stronger; separable from
specularis by its still larger and stouter build, less constricted thorax,
less marked lateral impressions, stouter antennae, more finely and
sparingly punctured elytra, and the more numerous and_ stronger
setae. Head pitchy-red, front rufescent, distinctly impressed on
either side, finely and sparingly punctured, sides with long, erect,
yellowish setae; ground-sculpture scarcely visible. Antennae
reddish-testaceous, the 2nd, 3rd and 4th joints subequal, short, 5th
as long as broad, 6th to 10th transverse gradually increasing in
width, 11th short-oval, acuminate. Thorax distinctly transverse;
widest just before the middle, the sides rounded and converging
anteriorly, contracted posteriorly in nearly a straight line, with
scarcely a trace of sinuation; posterior angles with a small oval
superficial impression, situated in front of which are two (as com-
pared with the general puncturation) large punctures; dise with an
60 Dr. Malcolm Cameron on
exceedingly fine groove in middle line posteriorly, feebly impressed
on either side; puncturation not so fine as on the head, sparing
and unequal, leaving a smooth impunctate median line; sides
with long yellowish setae; ground-sculpture longitudinal, strigose,
scarcely visible. Legs reddish-testaceous. Scutellum coriaceous,
with three or four minute punctures. Elytra about one-third
longer than, and as wide as, the thorax, scarcely transverse, on
either side of the suture with a fine stria; puncturation fine and
sparing as on the thorax, and, moreover, with a row of four larger
(especially the posterior pair) setiferous punctures parallel to the
stria, and three others on the middle of the disc; sides setiferous ;
ground-sculpture fine, coriaceous. Abdomen pitchy, the whole of
the last and the posterior margins of the rest of the segments
ferruginous; without punctures, except for the setiferous ones;
ground-sculpture distinct, coriaceous.
Hab. Woodlands, under bark.
3. Lispinus minutus, n. sp.
Pitchy-brown, head black; shining, coriaceous, impunctate.
Antennae and legs testaceous. Length 1:7 mm.
Head (including the eyes) a little broader than long, anterior
margin of the front very feebly emarginate, distinctly impressed on
either side; eyes rather large and prominent; sculpture coriaceous,
without trace of punctures, glabrous. Antennae moderate, the first
three joints subequal in length, decreasing in breadth, 4th monili-
form, 5th and 6th scarcely broader than long, 7th to 10th transverse,
gradually increasing in breadth, 11th short, oval. Thorax a little
transverse, a little narrower than the head (with eyes), broadest at
the anterior angles, sides almost parallel to the posterior third,
moderately constricted from thence to the rectangular posterior
angles; disc with a very narrow smooth median line throughout,
anterior margin on either side with a setiferous fovea, posterior
angles scarcely impressed; ground-sculpture coriaceous, a few
scarcely visible punctures traceable. Elytra longer than broad,
nearly half as long again as the thorax, obsoletely impressed on either
side of the sutural stria, and each with two minute foveae ; sculpture
‘as on the thorax. Abdomen pitchy, last segment entirely, the
posterior margins of the others, narrowly, reddish-testaceous;
sculpture coriaceous, no punctures other than the usual setiferous
ones.
Hab. Mandai, under bark, a single specimen.
New Species of Staphylinidae from Singapore. 61
OXYTELI.
4. Trogophloeus (s. str.) orientalis, n. sp.
Black nearly opaque, head and thorax densely punctured and grey-
pubescent; elytra distinctly longer than the thorax; first two
joints of the antennae and the legs testaceous. Length 2 mm.
In the dull, scarcely shining and pubescent surface this species
much resembles 7’. elongatulus, Er., but differs from it in the follow-
ing respects : the antennae are more elongate, the 5th and 6th joints
being longer than broad; the eyes are much larger and the temples
very small; the thorax is slightly longer, with the sides distinctly
less rounded towards the base, and the elytra are much longer.
Head transverse, impressed on each side in front within the antennal
tubercles; eyes very large, temples very small, densely punctured
and grey-pubescent. Antennae with the 2nd and 3rd joints sub-
equal, 4th to 7th all a little longer than broad, gradually decreasing
in length, 8th to 10th slightly transverse, gradually increasing in
breadth, 11th moderately elongate, oval; the first two joints clear
testaceous, the rest infuscate. Thorax a little broader than the
head, broadest at the junction of the first and second fourths, gently
rounded and narrowed anteriorly, narrowed posteriorly to the base
in an almost straight line; dise with four obsolete impressions, the
posterior pair being the more distinct; sculpture and pubescence
as on the head. FElytra broader and about one-fourth longer
than the thorax, much more finely and densely punctured than
in 7’. elongatulus. Abdomen a little widened posteriorly, densely
shagreened and grey-pubescent.
Hab. Keppel Harbour, in débris. One specimen.
It is possible that this species is synonymous with 7.
siamensis, Fauv., but not being certain from the description
I have thought it advisable to treat it as new.
5. Trogophloeus (s. str.) silvesiris, n. sp.
Black, moderately shining; fore-parts densely, finely punctured ;
thorax transversely impressed before the base and with four other
impressions on the dise; antennae slender, the first three joints,
legs and mouth-parts testaceous. Length 2 mm.
Facies of 7’. indicus, Kr., but. much smaller and with prominent
temples. Head large, transverse, subtriangular; temples smaller
than the diameter of the eyes, rather prominent; front with a short
impression within the antennal tuberosity on either side; vertex
with a small fovea on either side of middle line; densely, finely
62 Dr. Malcolm Cameron on
punctured. Antennae slender, all the joints distinctly longer than
broad, except the 10th which is but slightly elongate. Thorax
broader than the head, transverse, widest at the junction of the
anterior and second fourths, from thence strongly contracted pos-
teriorly in an almost straight line; disc with distinct transverse
impression before the base and in front of this the surface is so
impressed as to form an M-shaped elevation; on either side also are
two short, oblique impressions; puncturation similar to that of
the head. Elytra about one-third longer than the thorax, scarcely
transverse; disc on either side of the suture for the anterior two-
thirds with a longitudinal impression; puncturation similar to that
of the thorax. Abdomen not widened behind, exceedingly finely
and moderately closely punctured and pubescent.
Hab. Bukit Timah, Mandai and Sembawang, in débris,
on the banks of the jungle streams. Appears to be a
common insect.
6. Trogophloeus (Taenosoma) halophiloides, n. sp.
Nearly opaque, black; head and thorax densely shagreened,
impunctate ; first six joints of the antennae and legs pitchy-testace-
ous. Length 1:3 mm.
Very similar to the Palaearctie 7. halophilus, Kies., from which
it differs in the following respects : the shagreening and pubescence
of the head and thorax are coarser, the antennae much stouter, the
sides of the thorax more evenly rounded, the elytra much shorter,
slightly widened behind and a little more strongly punctured. Head
slightly narrower than the thorax, constricted behind, the temples
shorter than the diameter of the eyes, which are rather large; the
front longitudinally impressed on either side; the vertex with a
small, smooth, shining plaque, the rest of the surface densely
shagreened, without visible puncturation; pubescence rather coarse,
griseous. Antennae with the 2nd joint shorter than the Ist, the
3rd about half as long as the 2nd, the 4th to the 7th square,
the 8th to 10th transverse, the 9th to 11th larger than the
preceding.
Thorax transverse, widest at the junction of the anterior and
middle thirds, the side evenly rounded and converging both ante-
riorly and posteriorly, but more strongly so posteriorly; the dise
with four obsolete impressions; sculpture and pubescence as on
the head. Elytra a little longer than the thorax, transverse,
slightly widened behind; with puncturation and pubescence much
as in 7’. halophilus. Abdomen slightly widened behind, very finely
New Species of Staphylinidae from Singapore. 63
and pretty closely punctured, as in 7’. halophilus, and with similar
pubescence.
Hab. Pasir Panjang, on the beach, in débris.
7. Trogophloeus (Taenosoma) lucens, n. sp.
Black, shining, thorax and elytra chestnut brown; antennae,
mouth parts, and legs testaceous. Length 2:2 mm.
A shining insect, without trace of thoracic impressions. Head
transverse, black, distinctly constricted behind the temples, which
are a little prominent, their length much less than the diameter of
the eyes, the latter large ; the front on each side with a broad shallow
impression; puncturation fine and scanty, a rather broad area in
the middle line quite impunctate; no visible ground-sculpture ;
pubescence scanty, rather long and moderately coarse. Antennae
longer than the head and thorax, the Ist joint elongate, the 2nd
much shorter than the Ist, the 3rd a little shorter and more slender
than the 2nd, the 4th scarcely longer than broad, the 5th stouter
than the 4th and 6th either a little longer than broad or square, the
6th as long as broad, the 7th scarcely, the 8th to 10th gradually more
transverse, the 11th oval. Thorax brown, but little broader than
the head, almost semi-circular, widest at the junction of the first
and second fourths, from thence narrowed and rounded in front
and behind in an even curve, the sides passing insensibly into the
base, the anterior angles rectangular; disc without impressions,
but with a smooth impunctate line in the middle, the rest of the
surface moderately finely and not very closely punctured, the
punctures larger towards the sides, in which position several are
umbilicate; no visible ground-sculpture; pubescence as on the
head. Elytra brown, one-half as long again as the thorax, a little
broader than long, with moderately fine and not very close punctura-
tion, pubescence rather coarse, erect and moderately close; no
visible ground-sculpture. Abdomen slightly widened behind, black,
the posterior margins of the segments and the extreme apex more
or less brown; puncturation very scanty, scarcely visible ; ground-
sculpture coriaceous, distinct; pubescence rather long, sparing
and coarse.
Hab. Pasir Panjang, in a rotting pine-apple on a sandy
beach.
8. Trogophloeus (Taenosoma) littoralis, n. sp.
Castaneous, shining, elytra reddish-testaceous; thorax with four
impressions on the disc and the sides broadly impressed; mouth-
7
64. Dr. Malcolm Cameron on
parts, legs, and first three joints of the antennae reddish-testaceous,
the rest of the antennae fuscous. Length 1°75 mm.
A shining, reddish species, with lighter elytra, very similar in build
to 7. nitidus, Baudi, but with broader head, smaller eyes, and shorter
elytra. Head large, ferruginous, constricted behind, scarcely
narrower than the thorax; the front on either side with a well-
marked longitudinal impression; the temples slightly prominent,
their length equal to the diameter of the eyes; moderately finely
and not very closely punctured, and without visible ground-sculp-
ture; pubescence fine and sparing. Antennae longer than the head
and thorax, the 2nd joint about half as long as the Ist, the 3rd much
shorter than the 2nd, the 4th scarcely longer than broad, the 5th
square, larger than the 4th and 6th, the 6th moniliform, the 7th
and 8th slightly, the 9th and 10th more strongly, transverse, the 11th
conical. Thorax about one-half as broad again as long, broadest
at the junction of the first and middle thirds, from thence gradually
narrowed and rounded to the anterior angles, more strongly con-
tracted and much less rounded to the posterior angles; the disc
with four distinct impressions, the sides rather broadly and super-
ficially impressed; puncturation rather fine and not very close;
pubescence fine and scanty; no visible ground-sculpture. Elytra
reddish-testaceous, shining, one-fourth longer than the thorax,
transverse; puncturation coarser than that of the thorax, rather
superficial and moderately close; pubescence fine and moderately
close. Abdomen very sparingly, scarcely perceptibly punctured,
finely coriaceous, finely and sparingly pubescent.
Hab. Pasir Panjang, in rotting fruit on a sandy beach.
9. Trogophloeus (Taenosoma) rufotestaceus, n. sp.
Reddish-testaceous, moderately shining, antennae, mouth-parts
and legs testaceous, the last three joints of the antennae forming a
club. Length 1:4 mm.
A minute species, with large head, the abdomen more shining than
the fore-parts, and with the fourth visible segment somewhat pitchy.
Head large, subtriangular, constricted behind, a little wider than the
thorax; temples rounded, longer than the diameter of the eyes,
which are small; the front narrowly black between the antennal
tuberosities, slightly impressed on either side; sculpture finely
coriaceous, without trace of puncturation; pubescence very fine,
yellow, very sparing. Antennae about as long as the head and
thorax, the 3rd joint shorter than the 2nd, the 4th small, monili-
form, the 5th to the 8th transverse gradually increasing in width,
New Species of Staphylinidae from Singapore. — 65
the 9th considerably broader than the 8th, the 10th as broad as
the 9th, 11th conical. Thorax transverse, formed as in 7’. halophilus,
Kies., but shorter, widest at the junction of the first and middle
thirds, slightly rounded and narrowed anteriorly, more strongly
contracted backwards to the rounded posterior angles; disc longi-
tudinally impressed on either side of the middle line; sculpture and
pubescence similar to that of the head. Scutellum shining, im-
punctate. Elytra about one-fourth longer than the thorax, a little
infuscate posteriorly; sculpture finely granular and coriaceous, no
distinct puncturation visible ; pubescence yellow, fine and sparing,
but much more distinct than on the fore-parts. Abdomen very
finely coriaceous, impunctate, more shining than the fore-parts,
very finely and very sparingly pubescent.
Hab. Sembawang, on the bank of a stream.
10. Aploderus testaceus, n. sp.
Rufo-testaceous, shining: last six joints of the antennae and dise
of the elytra infuscate. Length 3°5-4 mm.
Head transversely suborbicular, front depressed between the
antennal tuberosities, anterior margin elevated and produced; eyes
large, their diameter much greater than the length of the temples ;
orbit with a juxta-ocular furrow; puncturation fine and sparing.
Antennae with the Ist joint elongate, clavate, the 2nd and 3rd
joints subequal, 4th slightly, the following more strongly transverse,
gradually increasing in breadth, the last joint conical. Thorax
transverse, a little broader than the head, widest just behind the
anterior angles, narrowed posteriorly in a nearly straight line,
posterior angles completely rounded; disc with a very fine median
impressed line (sometimes obsolete), sides broadly and feebly im-
pressed, puncturation exceedingly fine and sparing. Elytra a
little longer than the thorax, transverse, the puncturation closer
and more distinct than that of the thorax. Abdomen, except for
a few setiferous punctures, laevigate; ground-sculpture very fine,
coriaceous, scarcely visible.
3. Seventh ventral segment bluntly, triangularly produced in the
middle, and rather deeply emarginate on either side; the sixth
feebly impressed in the middle in front of the posterior margin,
the impression rather thickly punctured and clothed with stiff
whitish pubescence.
Hab. Mount Faber district, in dung. Appears to be
scarce.
TRANS. ENT. SOC. LOND. 1918.—PARTS I, II. (DEC.) F
66 Dr. Malcolm Cameron on
11. Oxytelus (Anotylus) granadillae, n. sp.
Pitch-brown, shining, thorax and abdomen pitchy-testaceous ;
first four joints of antennae and legs testaceous, the rest of the
former a little infuscate. Length 2°25-2°75 mm.
Build of O. kraatzi (pulcher, Kr.), but a little smaller than that
species, darker in colour, with the head entirely shining, ground-
sculpture coarser and limited to the frons and the part lying behind
the curved posterior line, puncturation of the thorax coarser and
more sparing, and the elytra less distinctly punctured; thorax also
less transverse. Head pitch-brown, in ¢ a little broader than the
thorax, transversely quadrate, clypeus depressed, semi-circular,
impunctate and without ground-sculpture; vertex with a short,
rather broad stria opening behind into a curved transverse line
limiting the region of the neck; eyes rather small, their diameter
shorter than that of the temples which are broadly rounded poste-
riorly ; very finely and sparingly punctured, finely wrinkled between
the antennal tubercles and about the neck, otherwise without ground-
sculpture. Vertex on either side with a fovea from which an
impressed line passes towards the posterior margin of the eye.
Mandibles reddish-testaceous, palpi testaceous. Antennae rather
long, of the same structure as in O. kraatzi, [st joint elongate,
gradually thickened towards the apex, 2nd longer and stouter than
the 3rd, 4th moniliform, 5th small and transverse, 6th to 8th slightly,
9th and 10th scarcely transverse, 11th oval. In the Q the head
is much smaller and not broader than the thorax, and the temples
are smaller. Thorax reddish-testaceous, shining, strongly trans-
verse, widest at the anterior angles, which are nearly acute, nar-
rowed in a straight line to just in front of the posterior angles, where
there is a feeble sinuation; disc with three furrows, the central
broadest in front and extending the whole length, the lateral furrows
curved and shorter; sides strongly impressed; puncturation rather
coarse, sparing, and rugose. Elytra transverse, shining, punctate-
strigose. Abdomen shining, very finely and sparingly punctured
and pubescent.
g. Seventh ventral segment slightly emarginate on either side of
the middle line posteriorly.
Hab. Keppel Harbour, in rotting Passion fruit.
12. Oxytelus (Anotylus) frugicola, n. sp.
‘
Reddish-testaceous, shining, abdomen pitchy; elytra simply
punctured, not at all strigose; antennae and legs testaceous.
Length 1-4 mm.
° New Species of Staphylinidae from Singapore. 67
Head in ¢ short, transversely quadrate, broader than the thorax,
front transversely impressed, smooth and polished; vertex with a
fine stria and with very few fine punctures, on either side with two
small rounded impressions placed transversely; temples and region
behind the antennal tubercles obliquely strigose-rugose; eyes
about the length of the temples, the posterior angles of which are
rounded. Antennae rather long, 2nd and 8rd joints of equal length,
4th as long as broad, 5th to 10th transverse, gradually increasing in
breadth, eleventh conical. Thorax transverse, widest a little behind
the anterior angles and from thence narrowed in a straight line
posteriorly, slightly rounded and narrowed in front, the straight
portion of the sides very obscurely crenulate; disc with three sulci,
the central straight and narrow, the others lightly curved and wider;
sides distinctly impressed; comparatively coarsely (for the size of
the insect), but not very closely, punctured; lateral impressions
rugose. Elytra longer than the thorax, transverse, testaceous,
shining, moderately finely and somewhat closely punctured, not at
all rugose or strigose. Abdomen dirty testaceous, shining, infuscate
on fifth and sixth segments, exceedingly finely and sparingly
punctured and pubescent.
g- There appears to be no special modification of the terminal
segments.
Hab. Mandai, a single specimen found in the rotting
fruit of a wild nutmeg.
13. Oxytelus (Anotylus) obseurus, n. sp.
Black, fore-parts entirely opaque, first three joints of antennae
and legs testaceous; anterior tibiae simple. Length 1:5 mm.
Smaller and more opaque than O. pygmaeus, Kr., the thorax much
narrower and the ridges not at allshining. Head transversely quad-
rate, narrower than the thorax; front impressed between the
antennal tubercles and coarsely strigose, the striate area bounded
by a fine shining line from the rest of the surface, which is com-
pletely opaque and densely, finely rugose-strigose ; base with trans-
verse impressed line bounding the neck; vertex without fovea or
stria. Antennae longer than the head and thorax, 3rd joint monili-
form, 4th small, transverse, 5th as long as broad, 6th to 10th gradu-
ally more transverse, 11th elongate, pointed. Thorax formed as
in O. pygmaeus, but considerably narrower; median sulcus narrow,
evanescent in front and behind, the lateral sulci double the width
of it and straight; sides rather broadly impressed; the whole
surface entirely opaque, with sculpture as on the head. Elytra
68 Dr. Malcolm Cameron on
longer and broader than the thorax, transverse, densely strigose-
rugose, impunctate, dull. Abdomen a little shining, exceedingly
finely and sparingly punctured and pubescent, with fine coriaceous
ground-sculpture.
g- Seventh ventral segment slightly produced and rounded in
the middle line.
Hab. Mount Faber, in carrion.
OsorIt.
14. Holotrochus nitidus, n. sp.
Black, shining, glabrous, sparingly but distinctly punctured;
antennae, legs and last segment of abdomen reddish-testaceous.
Length 3-3°5 mm.
Head convex, anterior margin rounded, front with a minute fovea
on either side; eyes moderately large, not prominent, temples
parallel; puncturation scattered, rather coarse. Antennae with
Ist joint elongate, stout, 2nd and 8rd subequal, 4th a little longer
than broad, 5th and 6th moniliform, 7th to 10th transverse, gradually
increasing in width, 11th conical. Thorax transverse, wider than
the head, broadest just behind the anterior angles and from there
very slightly rounded and narrowed to the obtuse posterior angles,
adjacent to which is a rounded impression ; puncturation as on head.
Scutellum bipunctate. Elytra a little longer than thorax, square,
puncturation less distinct than on the fore-parts. Abdomen very
finely and sparingly punctured, ground-sculpture finely coriaceous,
searcely visible. Anterior tibiae sinuate internally.
Hab. Mandai, in rotten wood.
STENINI.
15. Stenus (Tesnus) fortepunctatus, n. sp.
Black, very shining, glabrous, very coarsely punctured ; first four
joints of the antennae, palpi, and legs testaceous, the knees narrowly
infuseate. Length 3°75 mm.
Very similar in build to S. bispinus, Motsch., but much smaller,
with shorter abdomen, the terminal segments of which are more
strongly punctured, the head more concave, the antennae much
shorter, the fourth tarsal joints less strongly bilobed, and the thorax
a little shorter. Head large, not as broad as the elytra, completely
concave, without trace of central elevation, very coarsely and
closely punctured. Antennae rather short, the Ist and 2nd joints
New Species of Staphylinidae from Singapore. 69
of about equal length, the 3rd much longer, the 4th to the 8th all
longer than broad, gradually decreasing in length, 9th and 10th as
long as broad, the llth conical; the last seven joints infuscate.
Thorax widest at the middle, and from there gradually and equally
narrowed to the anterior and posterior angles; disc without trace
of impressions, coarsely punctured like the head. Elytra square,
convex, at the suture scarcely as long as the thorax, the sides
rounded, the posterior margins together distinctly emarginate ;
puncturation even coarser than that of the fore-parts. Abdomen
cylindrical, gradually pointed behind, bases of the segments strongly
constricted; the first four visible segments as strongly punctured
as the head, the following segments gradually less distinctly punc-
tured; anal spines short, incurved. Last joint of the tarsi distinctly
shorter than the first.
¢. Seventh ventral segment with acute triangular excision in the
posterior margin, sixth with a rather broad, thickly punctured and
pubescent impression occupying the whole length of the segment.
Hab. Mandai, in débris.
16. Stenus (Hypostenus) castaneus, Nn. sp.
‘Shining, head black; thorax and elytra dark brown; abdomen
with the first four and half the fifth segments chestnut-brown, the
rest black; first two joints of the antennae, and the legs, testaceous,
the:knees and base of the tibiae infuscate. Length 4 mm.
A slender species, very distinct by its colour and having somewhat
the facies of a small S. bispinus. Head black, glabrous, except for
some whitish pubescence on the front, rather deeply and longitudin-
ally impressed on either side of the vertex, which is elevated into a
rather broad, impunctate ridge, the latter with an elongate impres-
sion posteriorly; from the base of the antennal tubercle on either
side an impunctate ridge extends backwards and outwards towards
the eye; sculpture consisting of a few rather large, scattered punc-
tures. Antennae long and slender, all the joints considerably longer
than broad, the 3rd, 4th and 5th subequal, 6th, 7th and 8th gradually
shorter, 9th, 10th and 11th long, oval. Palpi testaceous. Thorax
dark pitchy-brown, widest at the middle; viewed from above,
narrowed anteriorly in a nearly straight line, posteriorly narrowed
and sinuate behind the middle, feebly impressed postero-laterally ;
anterior and posterior borders distinctly margined; disc without
impression, uniformly and rather coarsely punctured. Elytra dark
pitchy-brown, glabrous, broader than the head, as broad as long,
ample, convex, a little longer at the suture than the thorax, emargin-
70 Dr. Maleolm Cameron on
ate posteriorly, more coarsely punctured than the thorax. Abdo-
men cylindrical, the first four visible, and the basal half of the fifth,
segments castaneous, the rest black ; the first and fifth segments very
narrowly bordered, the first four strongly constricted at their bases ;
the first rather strongly punctured, the second to the fourth much
less strongly and less closely punctured, terminal segments almost
impunctate, the ninth broadly emarginate, its posterior angles
dentiform; anal styles slender, long, incurved, testaceous.
3S. Seventh ventral segment with an acute triangular excision, the
apex of which is rounded and the sides feebly margined; the sixth
impressed in the middle line at the base, the impression thickly
punctured and pubescent.
Hab. Mandai, on bank of a jungle stream and also in
damp wood.
PINOPHILI.
17. Pinophilus notabilis, n. sp.
Rufous, shining, head very finely and sparingly punctured;
thorax as long as broad, distinctly punctured; elytra one-third
shorter than the thorax, coarsely and rugosely punctured. Length
7°8 mm.
Of peculiar build, and from the description would appear to be
closely related to P. brachypterus, Kr., from which it apparently
differs in coloration and in both mandibles being furnished near the
base with a rather long sharp tooth. Head transverse, narrower
than the thorax, shining red, temples with a minute tooth, setiferous ;
front with three setiferous, punctures placed transversely, one
smaller, median, and one larger on either side ; vertex with four large
setiferous punctures placed quadrately, another pair obliquely placed
on either side near the base of the antennal tuberosities, and with
four or five others at the margin of the eye; besides these, there _
are some fine, scattered irregularly distributed punctures; ground-
sculpture fine, strigose, not very distinct. Mouth-parts testaceous,
mandibles ferruginous, falciform, each with a sharp tooth at the
base. Antennae pilose, the first two joints stouter than those follow-
ing, the 2nd a little shorter than the Ist, all the rest very slender
and narrowed at the base, 3rd slightly shorter than the 4th, 4th to
6th scarcely differing in length, slender and club-shaped, 7th to
10th gradually but slightly decreasing in length, 11th elongate, as
long as the 10th. Thorax as long as wide, broader than the head,
sides parallel, setiferous, anterior and posterior angles briefly rounded,
disc with trace of impunctate median line, otherwise uniformly
New Species of Staphylinidae from Singapore. 71
covered with moderately close, not very fine, digital * punctures;
ground-sculpture as on the head. Scutellum coarsely punctured,
Elytra narrower and one-third shorter than the thorax, coarsely
and rugosely punctured; pubescence long and scanty, yellow.
Abdomen pitchy-red, posterior margins of the segments narrowly
brighter; sides setiferous; puncturation rather fine, not very close,
the terminal segments almost as closely punctured as the anterior
ones; pubescence rather long, yellow; ground-sculpture imbricate
on the first two segments; anterior femora much thickened,
Hab. Bukit Timah, in a rotten log. A single 9.
18. Palaminus parvus, n. sp.
Shining, testaceous, puncturation large and superficial, abdomen
reddish-brown, thorax transverse, elytra longer than broad; an-
tennae, legs and palpi pale yellow. Length 2°75 mm.
Head transverse, puncturation rather large, superficial, almost
umbilicate. Antennae slender, first two joints of equal length,
stouter than the succeeding, 3rd a little longer than 4th, 4th and 5th
of equal length, longer than broad, 6th to 9th subequal, oval, 10th
stouter and longer than 9th, 11th obconical, broader than 10th.
Thorax broadest just behind anterior angles, about one-third broader
than long, gently rounded in front, narrowed in an almost straight
line to the rounded posterior angles, puncturation rather large,
sparing and superficial. Elytra more than one-third longer than
the thorax, distinctly longer than broad, much more closely punc-
tured than the fore-parts. Abdomen with first four segments
imbricate, 5th sparingly asperate, 6th laevigate, apex with a pair of
styliform processes. The whole insect clothed with long, coarse,
yellow hairs.
Hab. Bukit Panjang, in débris.
This species is somewhat similar in general appearance
and sculpture to P. insularis, Cam., from Jamaica, but the
thorax is less transverse and the elytra are shorter.
PAEDERINI.
19. Astenus orientalis, n. sp.
Reddish-testaceous, rather shining, antennae and legs pale tes-
taceous. Length 4 mm.
.
* By this term I mean an impression such as would be made by
pressure of the tip of the finger on a soft surface, such as putty or
elay.
72 Dr. Maleolm Cameron on
So closely allied to A. kraatzi, Bernh., that an enumeration of
the points of difference should suffice. It is a little more elongate
and the antennae are slightly longer than in A. kraatzi, the elytra
are unicolorous, parallel, more depressed on the disc and more
finely punctured, the abdomen is likewise unicolorous and more
finely punctured. The thorax has 4 and the elytra 7 or 8 strong
setae on either side as in A. kraatzi, and the anal styles are
similarly formed.
Hab. Bukit Panjang, in débris. A single .
20. Stilicopsis obliqua, n. sp.
Rufous, elytra testaceous, with an oblique pitchy-brown macula
extending from the lateral margins to near the apex of the suture ;
abdomen pitchy-testaceous, the fourth (visible) segment black;
antennae, legs and palpi pale testaceous. Length 4°5 mm.
Var. 1. Elytral markings almost obsolete, abdomen concolorous.
Var. 2. Uniformly reddish-testaceous.
Larger and much more robust than S. trinotata, Kr. Differs
from S. wmbilicata, Fauv., by the longer and more slender antennae,
longer and narrower thorax, shorter and broader elytra, and the
abdomen more widened behind. Head large, suborbiculate, temples
continuously rounded with the base, eyes prominent, sculpture close,
umbilicate. Antennae elongate, the 2nd joint shorter than the 3rd,
4th to 7th joints all considerably longer than broad, 10th almost
square, 11th conical. Thorax a little longer than broad, narrower
than the head and the elytra, puncturation as on the head; sides
with four or five long black setae. Elytra in fully-coloured speci-
mens with a pitchy indeterminate macula extending from the middle
of the sides and becoming more or less evanescent towards the apex
of the suture ; about as long as broad, convex, ample, rather coarsely
and closely punctured and pubescent; sides with three or four long
black setae. Abdomen slightly contracted at the base, reddish,
fourth visible segment pitchy-black, apex testaceous, puncturation
moderately fine and close, pubescence yellow, lateral setae black.
dg. Seventh ventral segment with a deep obtusely pointed exci-
sion, the sixth with a small obtuse excision.
Hab. Bukit Timah, in débris.
21. Stilicopsis persimilis, n. sp.
Rufo-testaceous, elytra testaceous, with obscure ill-defined pitchy
macula at the middle of the lateral borders; antennae, palpi and
legs pale testaceous. Length 4 mm.
New Species of Staphylinidae from Singapore. 73
ra
Closely resembling the preceding, S. obliqua, from which it is
distinguished by its smaller size, less robust build, and more shining
appearance ; the base of the thorax broader, the sides not so strongly
contracted, the dise slightly impressed throughout in the middle
line; the elytra a little less deeply punctured; the male-characters
also different.
g. Seventh ventral segment with a deep, acute, triangular exci-
sion, and the sixth segment with a minute notch, at the middle of
the posterior margin; metasternum in the middle in front of the
posterior coxae with a large, thickly punctured and pubescent
impression extending nearly to the middle coxae.
3
Hab. Bukit Timah, in débris. A single 3.
22. Thinocharis nigricans, n. sp.
Moderately shining, densely and finely punctured; pitchy-black,
head square, thorax pitchy-brown; antennae, palpi and_ legs
testaceous. Length 2:25 mm.
Smaller and narrower than 7’. carinicollis, Kr., and differently
coloured. Head as broad as long, quadrate, eyes small; temples
long, scarcely dilated, gradually passing into the rounded posterior
angles; base scarcely emarginate; puncturation very close and fine,
much closer and finer than in 7. carinicollis, Kr. Antennae with the
first two joints much thicker than the following, the 3rd to the 6th
longer than broad, subequal, 7th a little shorter than the 6th, 8th
to 10th short, scarcely longer than broad, 11th oblong-ovate. Thorax
pitchy-brown, narrower than in 7’. carinicollis, Kr., slightly longer
than broad, scarcely as wide as the head; anterior angles more
rounded than in 7’. carinicollis, Kr. ; disc with a narrow elevated line
posteriorly, which is finely grooved, obsoletely impressed on either
side; puncturation and pubescence similar to that of the head.
Elytra black, a little longer than the thorax, parallel, longer than
broad, densely and finely punctured and pubescent. Abdomen
black, apex of last segment brown, closely and finely punctured and
pubescent, but much less so than the fore-parts.
Hab. Bukit Timah, in débris.
23. Medon (s. str.) rubicundus, n. sp.
Shining, rufous, elytra testaceous, with the base and a variable
extent of the disc pitchy ; abdomen pitchy-red, the sixth and seventh
segments broadly reddish-testaceous posteriorly; antennae, palpi,
and legs reddish-testaceous. Length 4 mm.
74 Dr. Malcolm Cameron on
This species is possibly identical with M. discipennis, Fauv., but
would appear to differ in the finer puncturation of the thorax, which
is finer than that on the head. Rather robust. Head large, trans-
verse, quadrate, eyes moderate, the temples longer than their
diameter, parallel, posterior angles rectangular; vertex impunctate,
the front with a few fine scattered umbilicate punctures, the sides
and temples more closely and less finely punctured, the punctures
umbilicate and mixed with a few finer simple punctures; setae
black. Antennae scarcely as long as the head and thorax, the 2nd
and 4th joints shorter than the 3rd, 5th to 9th slightly transverse,
10th about as long as broad, 11th conical. Thorax a little narrower
than the head (especially in 3), slightly transverse, widest at the
anterior angles, narrowed almost in a straight line posteriorly ;
puncturation finer than on the head, superficial and scattered,
scarcely umbilicate; sides with seven or eight long black setae.
Klytra parallel, a little longer than the thorax, about as long as
broad, testaceous, less shining than the fore-parts, with an indeter-
minate triangular pitchy marking occupying the base and extending
more or less along the suture; puncturation close, fine and some-
what asperate; pubescence yellowish, setae black. Abdomen
pretty finely and closely punctured, with rather fine and long
pubescence.
3g. Seventh ventral segment with a narrow, deep, triangular
excision in the middle of the posterior margin; sixth segment
broadly and feebly emarginate.
Hab. Woodlands, in rotten logs.
24. Hypomedon fasciatus, n. sp.
Rufous, shining, elytra testaceous with broad transverse black
fascia; antennae, parts of mouth, and legs reddish-testaceous.
Length 3 mm.
From the description this insect would appear to be closely allied
to H. latecinctus, Fauy., but smaller and more brightly coloured.
Head large, transversely quadrate, eyes small, temples parallel,
posterior angles slightly rounded, vertex and front nearly impunc-
tate, sides and temples pretty closely and moderately strongly punc-
tured. Antennae rather short, 2nd joint shorter than 3rd, 3rd to
5th longer than broad, decreasing in length, 6th and 7th as long as
broad, 8th to 10th transverse, 11th elongate, oval. Thorax a little
narrower than the head, the median line obsolete, base with a small
feeble impression on either side, very finely and not closely punctured.
Elytra slightly broader than the thorax, a little longer than broad,
testaceous with a broad, well-defined, black band situated nearer
New Species of Staphylinidae from Singapore. 75
the posterior than the anterior border; puncturation not so fine as
on the thorax, but about as close. Abdomen reddish-testaceous,
pretty closely and finely punctured, less distinctly so posteriorly.
6. Seventh ventral segment with a deep narrow triangular excision
in the posterior margin.
Hab, Woodlands, under bark of decaying logs.
25. Hypomedon lucens, n. sp.
Reddish-testaceous, shining, abdomen pitchy-red. Antennae and
legs testaceous. Length 3 mm.
A subparallel-sided insect, the fore-parts clear shining reddish-
testaceous. Head large, transversely quadrate, temples parallel,
posterior angles bluntly rectangular; vertex impunctate, the rest
of the surface covered with large scattered umbilicate punctures ;
sides and front setiferous; no trace of ground-sculpture. Antennae
shorter than the head and thorax, 2nd joint shorter than the 3rd,
about as long as the 4th, 4th, 5th and 6th a little longer than broad
gradually decreasing in length, 7th as long as broad, 8th, 9th and
10th gradually increasing in breadth, 11th elongate, oval. Thorax
scarcely narrower than the head, transverse, disc with smooth
impunctate line throughout its length, the rest of the surface covered
with large scattered umbilicate punctures. Elytra a little longer
than, and as wide as, the thorax, scarcely longer than broad, of a
yellowish red colour, with rather fine, somewhat asperate and not
very close puncturation, sparingly pubescent. Abdomen pitchy-red,
very finely and not very closely punctured, pubescence yellowish,
rather long.
Hab. Bukit Panjang, in débris. <A single 9.
26. Hypomedon granulatus, n. sp.
Reddish-testaceous, shining, elytra broadly blackish at postero-
external angles; antennae, mouth-parts, and legs reddish-testaceous.
Length scarcely 2 mm.
Smaller and more shining than H. debilicornis, Woll., and differently
coloured, with a narrower head and thorax than in that species.
Head square, temples parallel, the posterior angles rather broadly
rounded, the, base emarginate ; sculpture consisting of small granules,
pretty dense on the front and temples, but becoming more scattered
posteriorly. Antennae short, the 3rd joint shorter than the 2nd,
4th scarcely longer than broad, 5th to 10th transverse, gradually
increasing in breadth, 11th short, oval. Thorax scarcely narrower
than the head, as long as broad, widest at the anterior angles, which
76 Dr. Malcolm Cameron on
are broadly rounded, narrowed in a straight line to the posterior
angles; dise with a narrow smooth elevated line, more distinct
posteriorly and becoming evanescent about the anterior third;
sculpture similar to that of the head; anterior angles with a single
seta. Elytra very slightly broader than long, a little longer and
distinctly broader than the thorax, of a testaceous colour, with the
posterior half of the sides, the postero-external angles, and the
posterior margins blackish; sculpture of the same character as that
of the head, but less distinct and not so close as on the thorax.
Abdomen very finely, sparingly and obsoletely punctured, especially
towards the apex; pubescence sparing, yellowish.
Hab. Mandai, in débris. The description is taken from
female examples.
PARASCOPAEUS, N. gen.
Labrum small, transverse, emarginate in front, sides rounded and
much contracted towards the base, almost obcordate; mandibles
strongly curved, prominent; third joint of maxillary palpi dilated,
four small, subulate; labial palpi 3-jointed.
Antennae inserted beyond the outer margin of the mandibles,
beneath the frontal margin, widely separated, much nearer the
eyes than to each other; the first joint long and stout, rather
broadly and deeply grooved on the upper surface from the apex
nearly to the base; eyes very small, not prominent; neck about
one-fourth the width of the base of the head; gular sutures dis-
tinct, separate, a little wider apart in front, otherwise parallel;
prosternum keeled in front of the anterior coxae, which, as well
as the others, are contiguous; anterior femora dilated, tibiae
obliquely truncate at their apices, finely setose; tarsi 5-jointed,
the anterior pair simple, the posterior pair with the first four joints
short, subequal; suture of elytra simple; abdomen keeled at the
base below, the sides margined above.
This genus would appear to stand between Dacnochilus
and Scopaeus; from the former it is distinguished by the
sulcate first antennal joint; from the latter by the broader
neck and differently shaped labrum. The specimen being
unique, a dissection of the mouth-parts has not been made.
OT iti
27. Parascopaeus nitidus, n. sp.
Shining, pitchy-brown; antennae, mouth-parts, legs, and pos-
terior margins of each abdominal segment and anus, testaceous.
Length 2:2 mm.
New Species of Staphylinidae from Singapore. 77
Facies somewhat like that of a minute Lathrobium. Head large,
quadrate, a little longer than broad; temples long, nearly parallel,
slightly contracted behind to the briefly rounded posterior angles ;
base truncate; disc with smooth, narrow, impunctate line through-
out; front and antennal tubercles reddish-testaceous, impunctate,
the rest of the surface moderately closely and, for a small species,
rather coarsely punctured; no visible ground-sculpture. Antennae
shorter than the head and thorax, the Ist joint rather long and
stout, deeply sulcate along the upper surface from apex nearly to
base, the 2nd short, clavate, the 3rd shorter than the 2nd, the
4th and succeeding joints transverse, the penultimate ones strongly
so, about three times as broad as long, the 11th not much longer
than broad. Thorax distinctly narrower than the head and elytra,
a little longer than broad, widest at the obtusely rounded anterior
angles, narrowed in a straight line to the rounded posterior angles ;
disc with a smooth central line throughout, which is finely grooved ;
puncturation fine and sparing, finely pubescent. Elytra distinctly
longer and broader than the thorax, longer than broad, a little
widened behind, finely, sparingly and indistinctly punctured,
finely pubescent. Abdomen slightly widened behind, finely,
indistinctly, and not closely punctured, sparingly pubescent.
dg. Last ventral segment with a deep, moderately broad,
triangular excision of the posterior margin; penultimate segment
with a small rounded emargination, in front of which is an oblong
impression extending for the whole length of the segment.
Hab. Bukit Panjang, in débris. A single 3.
28. Seopaeus niger, 1. sp.
Black, moderately shining; antennae with first six joints pitchy-
testaceous, the others clear testaceous; legs testaceous, the femora
more or less infuscate. Length 4 mm.
Facies of S. nitidulus, Motsch., but differently coloured, head a
little narrower, abdomen more slender, the antennae longer and
not so stout. A moderately robust and elongate form, entirely
black, with the abdomen more or less pitchy; occasionally the whole
insect is more or less pitchy black. Head large, convex, orbicular ;
temples passing insensibly into the base, puncturation very fine
and close. Antennae elongate, all the joints considerably longer
than broad, gradually decreasing in length, the 2nd joint shorter
than the 3rd, 4th to 6th subequal, 7th and 8th of equal length, 9th
and 10th likewise equal in length, 11th elongate, oval. Thorax
narrower than the head and elytra, oblong-ovate, the anterior
78 Dr. Malcolm Cameron on
angles not at all distinct, more shining than the head; dise dis-
tinctly carinate in the middle line posteriorly and impressed on
either side; puncturation very close, much finer than on the head,
almost imperceptible; pubescence very fine. Elytra parallel,
longer than the thorax, longer than broad, puncturation very fine,
close and asperate; pubescence fine and close. Abdomen a little
widened posteriorly, densely and very finely punctured, pubescence
fine and close; apex reddish-testaceous.
Hab. Mandai, on the bank of a stream. Four females.
29. Calliderma rufum, n. sp.
Rufous, elytra reddish-brown; head and abdomen shining, thorax
opaque; antennae and legs pale reddish-testaceous. Length
5-6 mm.
Near C. indicum, Kr., but larger and differently coloured, the
head longer in front of the eyes, the basal impression much broader,
and the abdomen more coarsely punctured. Head shining, elongate,
distinctly longer than the breadth including the eyes, the sides
parallel in front of these; temples small, strongly rounded and
passing insensibly into the base; the vertex posteriorly with a deep
semi-circular impression, from which on either side a sulcus passes
outwards to the orbit, and another, much wider behind, forwards,
nearly reaching the apex of the broad smooth triangular space
between the antennal tubercles; this space, the sulci, and the basal
impression, glabrous and highly polished, the rest of the surface
in front of the orbital sulci coriaceous, with a few large superficial
setiferous punctures; the surface behind the orbital sulci and the
temples without ground-sculpture, but with obsolete setiferous
puncturation. Antennae with the Ist joint as long as the five
following joints together, the 2nd to the 5th longer than broad,
gradually decreasing in length, the 6th and 7th moniliform, the 8th
to 10th slightly transverse, 11th short, oval. Thorax opaque, a
little longer than broad, slightly broader than the head, widest
just before the middle, the sides obtusely angulate at this point,
from thence rounded and converging anteriorly, sinuate and more
strongly converging posteriorly; disc in the middle line behind
with a short, shining longitudinally suleate carina, and on either
side with a sinuated, elevated line extending from the posterior
to the anterior margins, but not coalescing either with them or with
the median carina; the extreme ends of these lines are shining, and
except for these and the median carina, the whole of the surface
is opaque, densely and finely punctured; the sides with a few
New Species of Staphylinidae from Singapore. 79
setae; the lines on the disc are so curved as to resemble the outline
of a lyre. Scutellum shining, impunctate. Elytra about as long
as the thorax, a little longer than broad, not quite so dull as the
thorax, and more obscurely coloured; densely and closely, but less
finely punctured than the thorax. Abdomen pretty closely and
moderately coarsely punctured, especially at the bases of the
segments, more finely punctured posteriorly; pubescence rather
long, but not dense; anal styles testaceous, slightly curved upwards.
3g. Seventh ventral segment with a deep, narrow, triangular
excision in the posterior margin, the sides of which are finely
bordered.
Hab. Bukit Timah, on the bank of a jungle stream.
30. Calliderma nitens, n. sp.
Rufous, shining, elytra black, less polished; legs, palpi, and
antennae testaceous, the apex of the Ist, and the whole of the 2nd,
3rd and 4th joints infuscate. Length 5 mm.
A very shining insect, with glabrous, impunctate thorax, and
dark elytra, except for the extreme base, which is shining and
rufescent. Head shorter than in C. ru/wm, the temples longer,
straighter and converging, the impression on the vertex triangular ;
puncturation sparing, obsolete and setiferous, the antennal tuber-
osities and the sides of the head in front of the eyes with coriaceous
ground-sculpture; the front, the space between the antennal
tubercles, and the immediate vicinity of the median sulcus and the
temples, without ground-sculpture. Antennae longer and more
slender than in C. rufum, with the Ist joint about equal to the five
following joints together, the 2nd a little shorter than the 3rd,
the 3rd to the 9th all distinctly longer than broad, gradually de-
creasing in length, the 10th as long as broad, the 11th short, oval.
Thorax narrower than in C. rufum, the sides more sharply angu-
late and without trace of puncturation or ground-sculpture ; the
dise with a sulcate carina extending from the base almost to the
level of the widest part, where it opens out into a longitudinal
impression that extends almost to the anterior margin, and on either
side with a raised sinuate line, which in. front turns inwards to join
its fellow limiting the median impression and separating it from the
anterior margin, and behind likewise unites with its fellow and the
median carina; sides strongly impressed behind the anterior angles ;
the lyre-shaped pattern formed by the raised lines not so obvious
as in some of the other species of the genus, this being due to the
uniformly shining surface. Scutellum red, impunctate. Elytra
80 Dr. Malcolm Cameron on
about as long as the thorax, longer than broad, parallel; the extreme
base shining, rufescent, and very sparingly punctured, the rest
blackish, not very shining, glabrous, densely and not very finely
punctured. Abdomen rufous, moderately finely and not very
closely punctured on the anterior segments, especially at their
bases; pubescence rather long, yellowish; anal styles testaceous,
up-curved.
3. Seventh ventral segment with a deep, narrow, triangular
excision in the middle of the posterior border, the apex of which
is rounded and the sides not margined.
Hab. Mandai, on the bank of a jungle stream.
31. Calliderma rugicolle, n. sp.
Black, rather shining; thorax in front narrowly, behind much
more broadly, red; abdomen red, the fourth (visible) and greater
part of the fifth segments pitchy-black; antennae, palpi and legs
testaceous, the 2nd, 3rd and 4th joints of the former, infuscate.
Length 5 mm.
From the description this species would appear to be allied to
CO. aspericolle, Fauv. Head narrower than in ©. indicum, Kr.,
with the temples straighter and convergent, and the occipital fossa
rhomboidal; the front and the triangular smooth space between
the antennal tuberosities shining, reddish-testaceous, without visible
sculpture; the rest of the surface (except in the immediate vicinity
of the longitudinal sulcus, occipital fossa, and the temporal regions)
coriaceous, with obsolete setiferous puncturation, more distinct on
the temples. Antennae long, the Ist joint as long as the five follow-
ing joints together, the 2nd a little shorter than the 3rd, the 2nd
to the 9th all distinctly longer than broad, gradually decreasing in
length, the 10th scarcely longer than broad, 11th short, ovoid.
Thorax distinctly longer than broad, obtusely angulate before the
middle, narrowed from thence anteriorly in a nearly straight line,
and posteriorly in a straight line; disc in the posterior third with a
broad, deeply grooved keel, anteriorly with a digital impression ;
the raised lateral lines distinct throughout, turned inwards and
confluent with the central carina posteriorly, and with the margins
of the digital impression anteriorly; the sides with rather obsolete
impression behind the anterior angles; puncturation coarse, rugose
and confluent, wanting on the anterior border, the digital impression
and the spaces between the central keel and the lateral lines, all
of which are completely smooth and shining; the surface red,
with a narrow black fascia nearer the anterior than the posterior
border. Scutellum red, shining, impunctate. Elytra black, rather
my
New Species of Staphylinidae from Singapore. 81
shining, longer than broad, parallel, about as long as the thorax,
very closely and moderately coarsely punctured (more strongly
than in C. indicum). Abdomen shining, finely and_ sparingly
punctured throughout, less distinctly so posteriorly; anal styles
testaceous and curved upwards.
Hab. Mandai, on bank of a jungle stream. A single 9.
32. Cryptobium foveatum, n. sp.
Black, shining, fore-parts closely and coarsely punctured ; abdo-
men rather less shining, finely and closely punctured; antennae
reddish-testaceous; legs pale testaceous. Length 8°5 mm.
Very near C. fossigerum, Kr., but larger and more robust, rather
more shining and with still coarser puncturation and longer antennae,
the first joint of which is unicolorous. Head oblong, temples
parallel, posterior angles rounded, puncturation coarse, close and
umbilicate; space between antennal tuberosities smooth and
shining; pubescence fine. Antennae unicolorous, pale reddish-
testaceous, Ist joint fully equal to the three following together,
the 2nd shorter than the 3rd, 4th to 10th all longer than broad,
gradually decreasing in length, the penultimate joint but slightly
longer than broad, 11th as long as broad. Thorax nearly cylindrical,
feebly rounded towards the anterior angles, the smooth median line
broken anteriorly; puncturation as on the head; pubescence
griseous. Scutellum punctured. Elytra as long as the thorax,
coarsely and closely punctured. Abdomen closely punctured
throughout, more coarsely so anteriorly, especially at the bases
of the segments; pretty thickly clothed with rather long greyish
pubescence.
g: Seventh ventral segment with a rather broad triangular
emargination; the sixth with a large, deep, round fossa, clothed
with long converging hairs, in the middle of the base; the posterior
border slightly produced in the middle line, and bearing a feeble
tubercle, slightly emarginate on either side; the space between
the fossa and the posterior border impressed and glabrous.
Hab, Singapore town, at light. A single specimen.
XANTHOLININI.
35. Oligolinus parvus, n. sp.
Black, shining; antennae, mouth-parts and legs reddish-tes-
taceous, the femora and middle and posterior tibiae more or less
pitchy. Length 4 mm.
TRANS. ENT. SOC. LOND. 1918.—PART™ I, II. (DEC.) @G
82 Dr. Maleolm Cameron on
Allied to O. leucocnemis, Kr., but much smaller and narrower,
more depressed and with shorter head, the posterior angles of which
are much less broadly rounded, differently coloured legs, and the
thorax much more narrowed behind. Head quadrate, temples
parallel, the posterior angles briefly rounded, the median sulci very
short and broad, foveate, the orbital sulci short and oblique ;
punctures very few, fine, and scattered, four rather larger ones
placed quadrately on the vertex; ground-sculpture scarcely per-
ceptible, strigose. Antennae short and stout, the 2nd joint not
much longer than broad, the 3rd to 10th transverse, the pen-
ultimate ones strongly so. Thorax scarcely broader than the head,
distinctly longer than broad, the sides contracted in a straight line
posteriorly from the obtusely rounded anterior angles; the disc
on either side with an irregular series of six small punctures, and
externally with a curved row of four still finer ones; ground-
sculpture as on the head. Scutellum quadripunctate. Elytra as
long and as broad as the thorax, parallel, often more or less brownish
near the sutural and apical margins; exceedingly finely and spar-
ingly punctured; suture imbricate. Abdomen shining, exceedingly
finely and sparingly punctured; pubescence yellowish, rather
coarse and sparing.
(7). Sixth ventral segment obtusely produced posteriorly and
feebly sinuate on either side.
Hab. Keppel Harbour, a single specimen in débris.
Woodlands, under bark.
34. Somoleptus linearis, n. sp.
Shining, head and abdomen black, thorax and elytra pitchy-
browi; antennae, mouth-parts and legs testaceous. Length 3 mm.
A smaller and narrower insect than S. parvulus, Sharp. Head
black, wider than the thorax, longer than broad; temples almost
parallel, very slightly widened towards the posterior angles, which
are rather broadly rounded; eyes much shorter than the temples ;
base truncate, neck slender, about one-fourth the breadth of the
head; frontal furrows parallel, not well marked, the lateral wanting,
the orbital linear, oblique, passing backwards and inwards towards
the middle line; puncturation moderately close and fine on the
temples, rather coarser in front behind the furrows, the middle of
the disc impunctate; no visible ground-sculpture. Antennae short
and stout, the Ist joint long and thick, the 2nd about one-fourth
the length of the Ist, the 3rd to the 10th transverse, increasing in
width, the penvltimate ones nearly discoidal, 11th short, conical.
New Species of Staphylinidae from Singapore. 83
Thorax narrow and elongate, nearly half as long again as broad,
widest at the anterior angles, which are rounded, the sides but
slightly converging in a straight line to the posterior angles, which
pass insensibly into the base; puncturation as on the head, and
leaving a narrow impunctate median space throughout; sides with
a few fine setae; pubescence fine and sparing. Scutellum triangular,
impunctate; transversely strigose. Elytra pitchy-brown, lighter
about the suture, which is imbricate, as long as the thorax, and a
little longer than broad; sparingly and finely punctured ; pubescence
fine, stiff, and griseous. Abdomen pitchy, the apex and posterior
margins of the segments narrowly lighter, very sparingly and finely
punctured; pubescence rather long, stiff, griseous.
Hab. Bukit Panjang, in rotten logs. The specimens
examined do not appear to present any visible sexual
characters.
35. Eulissus lateralis, n. sp.
Black, shining, elytra and abdomen pitchy, the former obscurely
testaceous on the disc, the latter with the lateral margins clear
testaceous; antennae, mouth-parts and legs reddish-testaceous,
the tibiae a little infuscate. Length 7 mm.
A very distinct species, the lateral margins of the segments of
the abdomen being bright testaceous yellow. Head, black, shining,
subquadrate, the temples parallel, the posterior angles with a minute
tooth; median sulci parallel, extending to the same level as the
lateral ones, these passing backwards and slightly outwards, and
connected with a short oblique orbital furrow, the juncture being
marked with a large umbilicate puncture; temples bounded above
by a deep, rather broad furrow extending from the posterior margin
of the orbit to the posterior angles, the furrow provided with two
or three large umbilicate setiferous punctures; sculpture consisting
of larger and smaller, scattered and irregular punctures, the space
between the median sulci impunctate; temples grooved longi-
tudinally; no visible ground-sculpture. Antennae short, the
2nd joint subequal to the 8rd, the 4th strongly transverse, as are
the following joints, which, however, do not increase in breadth
towards the apex, the 11th short, oval. Thorax formed as in #.
anachoreta, Er., with three punctures on each side—one at the
anterior angles, one at the posterior angles and one on the anterior
margin—otherwise impunctate and without ground-sculpture.
Scutellum shining, with three or four somewhat asperate punctures.
Elytra as long as the thorax, longer than broad, pitchy, the posterior
two-thirds of the pleura and an indeterminate macula on each disc
84 Dr. Maleolm Cameron on
more or less testaceous; sculpture consisting of a sutural row of
fine somewhat obsolete punctures, and a distinct row from the
humeral angle to the posterior margin of about twelve punctures ;
the pleura have also an irregular series of eight or nine punctures,
otherwise the surface is impunctate and shows no sign of ground-
sculpture. Abdomen pitchy, the extreme apex, the posterior
margins of the segments very narrowly, and the explanate lateral
margins entirely, bright yellow-testaceous; puncturation very
fine and sparing; pubescence stiff and scanty.
Hab. Woodlands, in dry dung. A single 9.
36. Diochus pulchellus, n. sp.
Pitchy-black, shining; thorax entirely, apex of elytra broadly
reddish-testaceous; abdomen pitchy-red, the apex testaceous;
antennae, mouth-parts, and legs testaceous. Length 3 mm.
A brightly-coloured, shining insect. Head subtriangular, longer
than broad; front with a minute tubercle in the middle line on a
level with the bases of the antennal tuberosities; sculpture con-
sisting of a row of four punctures on either side—one at the base
of the antennal tuberosity, a second a little behind the level of the
posterior border of the eye, a third at an equal distance from the
second as this is from the first, and a fourth in front of the base of
the head; temples with a few fine setiferous punctures; ground-
sculpture very fine, transverse, strigose. Antennae reaching the
posterior margin of the thorax, the 2nd and 3rd joints of equal
length, 4th and 5th subequal, a little longer than broad, the 6th
as long as broad, the 7th scarcely, the 8th to 10th slightly, transverse.
Thorax red, widest at the rounded posterior angles, longer than
broad, the sides slightly converging anteriorly to the widely rounded
anterior angles; disc with a row of three setiferous punctures con-
verging behind on either side, and also with two externally near the
anterior angles, and a minute one at the posterior angles; the sides
setose. Elytra pitchy-black, shining, the sides, posterior angles
and apical margin broadly reddish-testaceous; shorter than the
thorax, transverse, widened posteriorly; sculpture consisting of a
row of four or five obsolete, scarcely visible setiferous punctures
on each disc; sides with rather long dark setae. Abdomen pitchy-
red, the 5th (visible) segment reddish-testaceous, the 6th testaceous ;
finely and closely punctured and pubescent throughout, the sides
setiferous, each segment also with erect setae.
Hab. Sembawang, in débris. Unique.
Le) (
New Species of Staphylinidae from Singapore. 8:
pe gay
STAPHYLININI.
37. Holisus parvus, n. sp.
Depressed, linear, shining pitchy-brown; elytra obscure testa-
ceous; the first three joints of the antennae fusco-testaceous ; legs
testaceous.
Length 2-3 mm.
Head large, a little longer than broad; temples parallel, the
posterior angles briefly rounded; eyes small; front truncate ;
puncturation (for a small species) rather large superficial, feebly
umbilicate and rather close on the disc, temples almost impunc-
tate; pubescence fine, sparing; mouth-parts pitchy-testaceous.
Antennae rather short, the 2nd and 3rd joints of equal length, the
4th as broad as long, the 5th slightly transverse, the following
joints gradually but slightly increasing in breadth, 11th oval.
Thorax narrower than the head, slightly transverse trapezoidal,
widest at anterior angles, narrowed in a straight line to the rounded
posterior angles; disc broadly but feebly impressed posteriorly ;
puncturation very fine and not very close; pubescence fine, less
sparing than on the head. Elytra slightly widened behind, a little
longer than broad, wider than the thorax, obscure testaceous more
or less infuscate about the scutellum and sides; puncturation and
pubescence very similar to that of the thorax. Abdomen a little
widened behind, the first three visible segments finely and moder-
ately closely, the following much more finely and sparingly, punc-
tured; pubescence fine and sparing.
Hab. Mandai.
One specimen found under bark.
38. Holisus cingulatus, n. sp.
Pitchy-black, scarcely shining, the thorax, 2nd, 3rd, 4th, 8th
and posterior portion of the 7th abdominal segments and legs
reddish-testaceous ; first two joints of the antennae pitchy-testaceous.
Length 1:75 mm.
A very small, narrow, parallel-sided insect, at once distinguished
from the preceding by the colour, smaller size, and shorter head.
Head large, massive, square, very slightly dilated at the temples,
which are long, with rounded posterior angles; disc broadly im-
pressed towards the front; puncturation rather fine, superficial and
moderately close, obsoletely umbilicate ; finely pubescent. Antennae
short, the 2nd joint shorter than the Ist, the 3rd much shorter than
86 Dr. Maleolm Cameron on
the 2nd, the 4th to the 10th transverse, increasing in breadth, the
penultimate three times broader than long, the 11th conical. Thorax
shorter and a little narrewer than the head, transverse, widest at
the anterior angles, the sides converging in a straight line to the
rounded posterior angles; the disc rather broadly impressed in the
middle throughout its length; puncturation very fine and rather
close; finely pubescent. Elytra scarcely longer but a little broader
than the thorax, square, pitchy, obscurely lighter on the disc;
puncturation very fine and rather close ; finely pubescent. Abdomen
slightly widened behind, finely and sparingly punctured and pubes-
cent throughout.
Hab. Bukit Timah.
One specimen, taken from beneath bark.
39. Actobius laticeps, n. sp.
Black, shining; antennae and legs fuscous, the Ist and 2nd joints
of the former and the femora, testaceous. Length 4 mm.
More slender, with more pointed abdomen, broader head and
thinner antennae than A. signaticornis, Muls. Head large, quadrate,
slightly transverse; the temples slightly converging to the rounded
posterior angles; moderately finely and rather sparingly punctured,
a broad area from the front to the base in the middle quite im-
punctate; punctures setiferous; the eyes larger and more prominent
than in A. signaticornis; no ground-sculpture visible. Antennae
slender, the 2nd joint dilated, shorter than the 3rd, the others dis-
tinctly longer than broad, gradually decreasing in length. Thorax
a little narrower than the head with the eyes, widest at the broadly
rounded anterior angles, narrowed posteriorly in a straight line,
slightly longer than broad; dise with a somewhat irregular row of
seven or eight moderately-sized setiferous punctures on either side,
externally finely, sparingly and irregularly punctured. Scutellum
triangular, sparingly punctured. Elytra a little longer than the
thorax, slightly longer than broad, finely, asperately and some-
what sparsely punctured, more finely and not so closely punctured
as in A. signaticornis. Abdomen closely and finely punctured and
pubescent throughout, the posterior margins of the segments
narrowly and obscurely reddish; the puncturation not so dense
and fine as in A. signaticornis.
3. Anterior tarsi dilated; the last ventral segment with a small
triangular excision at the posterior margin.
Hab. Mandai, on the bank of a jungle stream,
New Species of Staphylinidae from Singapore. — 87
40. Philonthus suleatus, n. sp.
Black, shining; suture of elytra, first joint of the antennae and
the legs rufo-testaceous, the tibiae a little infuscate; penultimate
joints of the antennae as long as broad; front of the head deeply
sulcate ; dorsal series of thoracic punctures five * in number. Length
65-7 mm. Build of P. sanguinolentus, Grav., but with smaller head,
stouter antennae, and much less closely punctured abdomen. Head
suborbicular; eyes not prominent, viewed from above, their length
less than that of the temples; front in the middle line with a deep
longitudinal sulcus reaching to the anterior margin; the median
intra-ocular punctures much further apart from one another than
from the lateral ones; temples with four or five setiferous punctures ;
ground-sculpture fine, transverse, strigose. Antennae with the Ist
joint and base of the 2nd reddish-testaceous, the 3rd scarcely longer
than the 2nd, the 4th to the 7th each a little longer than broad,
gradually decreasing in length, the 8th to the 10th about as long as
broad, 11th short, oval. Thorax scarcely longer than broad, a
little wider than the head, the sides parallel, scarcely converging in
front; disc with a series of five rather large punctures on either
side, of which the anterior and posterior ones are further apart
from the rest of the series; the sides with five punctures—three
near the anterior angles, and two external to the dorsal row.
Scutellum very finely punctured and pubescent. Elytra as long as
the thorax, bronze-black, shining, the suture distinctly and sharply
reddish-testaceous; less finely and less closely punctured than in
P. sanguinolentus, pubescence rather long and yellowish. Abdomen
iridescent, finely but not very closely punctured throughout;
pubescence rather long, coarse and griseous; posterior margins of
the ventral segments reddish-testaceous. First joint of posterior
tarsi scarcely longer than the last, about equal to the two following
joints united.
g. Anterior tarsi simple; sixth ventral segment feebly emarginate
in the middle of the posterior border,
Hab. Keppel Harbour, in débris.
41. Philonthus castaneipennis, n. sp,
Black, shining, thorax and elytra chestnut-red, the latter scarcely
infuscate at the postero-external angles; abdomen pitchy; an-
tennae and mouth-parts reddish-testaceous, legs testaceous-yellow ;
thorax with dorsal series of five punctures. Length 6 mm,
are
* Including the anterior puncture in the series,
88 Dr. Malcolm Cameron on
Near P. circumductus, Fauy., but rather more robust, with longer,
uniformly coloured antennae and reddish thorax. Head _ trans-
versely quadrate, widest across the eyes, temples slightly con-
verging posteriorly, the posterior angles rounded; median pair of
intra-ocular punctures much further from each other than from the
lateral ones, the disc with two obliquely placed punctures on either
side and a group of three or four near the postero-internal border
of each eye; all the punctures setiferous. Antennae nearly as
long as the head and thorax, the 2nd joint a little shorter than the
3rd, 4th a little longer than broad, 5th as long as broad, the 6th to
10th scarcely transverse, the L1th oblong-oval, acuminate. Thorax
about as broad as the head, very little narrower at the anterior
angles, the sides nearly straight; disc with a row of five rather
small setiferous punctures, of which the second and third are more
approximate than those of the rest of the series; sides with a
curved row of three other punctures and a fourth puncture just
behind the anterior angle; posterior margin with a row of fine
setiferous punctures also. Scutellum distinctly and sparingly
punctured, as in P. circumductus. Elytra a little broader than,
and as long as the thorax, square, of a bright reddish-chestnut
colour, appearing in certain lights obscurely darker at the postero-
external angles; finely, asperately, and sparingly punctured, as
in P. circumductus; all the punctures setiferous. Abdomen dark
pitchy-red, the extreme margins of the segments obscurely tes-
taceous; puncturation sparing and setiferous, the bases of the
segments less closely punctured than in P. circumductus. First
joint of posterior tarsi scarcely as long as the last joint.
G. Anterior tarsi dilated; sixth ventral segment with a triangular
impression, the base (which corresponds to the posterior margin)
rather deeply emarginate.
Hab. Mandai, in rotting fungus.
42. Philonthus belonuchoides, n. sp.
Depressed, black, rather shining; first joint of antennae, tibiae
and tarsi obscure testaceous, coxae pitchy, femora clear testaceous ;
thorax with dorsal series of five punctures. Length 8-8°5 mm.
In build this species presents a remarkable resemblance to
Belonuchus mutator, Fauv. Head broad, transverse, widest across
the eyes, the temples very slightly converging to the briefly rounded
posterior angles; vertex with a deep, broad, longitudinal rhomboidal
impression, the median intra-ocular punctures a little more distant
from each other than from the lateral ones; dise posteriorly with an
New Species of Staphylinidae from Singapore. 89
7 ga}
oblique row of three punctures on either side, and two or three more
punctures behind the eyes and on the temples; ground-sculpture
fine, transverse, strigose. Antennae about as long as the head and
thorax, the 2nd joint scarcely shorter than the 3rd, the 4th to the
6th slightly longer than broad, decreasing in length, the 7th to the
9th as long as broad, 10th scarcely transverse, the 11th short,
oblong oval, emarginate below. Thorax as long as broad, widest
at the anterior angles, which are depressed and obtuse, the sides
(viewed from above) converging in a straight line to the rounded
posterior angles; disc on either side with a row of five large
punctures, of which the fifth is more remote, externally with a curved
row of three smaller; ground-sculpture as on the head. Scutellum
moderately coarsely and rather closely punctured, and with long
yellowish pubescence. Elytra shining, a little broader than, and
as long as, the thorax, slightly longer than broad, rather finely and
by no means closely punctured; pubescence yellowish. Abdomen
finely, but not very closely punctured and pubescent throughout.
First joint of posterior tarsi about as long as the last joint.
3S. Anterior tarsi simple; head much larger, broader than the
thorax; sixth ventral segment with a shallow emargination of
the posterior border; the fifth segment produced, narrowed and
rounded in the middle, the border set with short black setae.
Hab. Keppel Harbour, in débris and dry dung.
43. Orthidus cupreipennis, n. sp.
Shining brassy-bronze, elytra copper-bronze; antennae, mouth-
parts, and legs, ferruginous. Length 10 mm.
Almost identical in build with O. cribratus, Er., but smaller and
differently coloured. Head shining, brassy-bronze, slightly trans-
verse, quadrate, fully as broad as the thorax, the median pair of
intraocular punctures much larger than the lateral, about equi-
distant; vertex with a large puncture on either side of the middle
line; the temples pretty closely and rather coarsely punctured and
setiferous; the dise with a few exceedingly, fine scattered points ;
ground-sculpture very fine, strigose. Antennae ferruginous, the
upper surface of the Ist joint infuscate; the structure the same as
in O. cribratus. Thorax brassy-bronze, as long as broad, distinctly
wider at the anterior angles, which are rectangular, narrowed in a
straight line to the rounded posterior angles; disc with a series of
four rather large punctures on each side, of which the first is more
remote from the second than this is from the third; anterior margin
with a small puncture on either side; anterior angles with a group
90 Dr. Malcolm Cameron on Staphylinidae from Singapore.
of five or six punctures; no visible ground-sculpture. Scutellum
closely and rather coarsely punctured. Elytra copper-bronze,
longer than the thorax, a little longer than broad, less shining than
the fore-parts; coarsely and closely punctured as in O. cribratus.
Abdomen pitchy-black, margins of the segments obscurely and
narrowly reddish; moderately coarsely and somewhat thickly
punctured and pubescent, as in O. cribratus; ground-sculpture
distinct, transverse strigose. Under surface reddish-castaneous.
Hab. Pasir Panjang, in seaweed. A single 9.
(QUEDIINI,
44. Acylophorus rotundicollis, n. sp.
Black, shining, abdomen iridescent. Thorax with strongly
rounded sides, the disc with a single puncture on either side of the
middle line. Femora and tarsi dark testaceous, the tibiae pitchy.
Length 6-7 mm.
Very similar in general appearance to A. glaberrimus,
Herbst., of Europe, but differs as follows: the head is
much narrower, the disc has a very few very fine punc-
tures, and the temples are rather closely’ punctured; the
antennae are less stout, but of similar build; the thorax
is broader, with more strongly rounded sides, and the disc
has a single large puncture on either side of the middle
Ime and a very minute one towards the anterior angles;
the elytra are transverse, shorter and a little more coarsely
punctured; the abdomen is distinctly iridescent and less
finely punctured; and the legs are lighter.
Hab. Bukit Timah.
Found in flood débris.
(To be continued.)
IIT. Australian Braconidae in the British Museum. By
Row LanpD EK. Turner, F.Z.S8., F.E.S.
[Read February 6th, 1918.]
Subfamily BRACONINAE.,
STIGMATOBRACON, gen. nov.
SCAPE ovate, nearly twice as long as the greatest breadth, antennae
as long as the whole insect or longer. Head transverse, eyes
moderately large. Parapsidal furrows shallow, but distinct.
Abdomen longer than the head and thorax, parallel sided, rather
elongate ; first tergite much longer than broad, with a deep longi-
tudinal groove on each side; second tergite without a median area,
with a deep oblique groove on each side from the base tothe apical
angles, the grooves nearer to each other at the base than to the
anterior angles, the segment as long as its apical breadth; second
suture feebly crenulate; the whole abdomen smooth and shining,
the sutures, except the second, shallow and smooth. Terebra
short and very stout, not more than one-third of the length of the
abdomen, slightly curved downwards, the valvulae broad, especially
at the apex and pubescent. Sternites 1-4 longitudinally carinate
in the middle; the fifth sternite large, with a median longitudinal
sulcus, narrowly emarginate at the apex and projecting much be-
yond the apex of the abdomen, so that the terebra has the appear-
ance of originating on the dorsal surface instead of ventral. Third
tergite with the basal angles only very indistinctly divided from the
rest of the segment. Nervulus interstitial; first abscissa of the
cubitus almost straight; first discoidal cell almost as high at the
apex as at the base; stigma large, the radius originating before the
middle; first abscissa of the radius very short, second very long;
radial cell almost reaching the apex of the wing. Hind and inter-
mediate tarsi no longer than the tibiae.
KEY TO THE SPECIES.
1. Stigma yellow. 2.
Stigma black, with a very small yellow
spot atthe base. . .». . . . S. torresensis, Turn.
2. Wings wholly dark fuscous, except
the stigma. . . . «. . . «. « S. xanthostigma, Turn,
Wings more or less yellow at the base. 3.
TRANS. ENT. SOC. LOND. 1918.—PaARTS I, HW. (DEC.)
92 Mr. Rowland E. Turner on
3. Mesosternum and the greater part of
the hind and intermediate legs
black: 2. i isl) e sue) 3 os os OS. diversipennisy Durn:
Thorax and legs wholly testaceous red. S. basipennis, Turn.
Type of the genus S. xanthostigma, Turn.
Stigmatobracon xanthostigma, sp. n.
2. Rufa, capite, abdomine, tarsisque posticis nigris, segmentis
abdominalibus duobus basalibus rufis, secundo apice nigro; mandi-
bulis palpisque testaceis; alis fuscis, stigmate flavo.
Long. 15 mm.; terebrae long. 3 mm.
®. Face shining, shallowly and rather sparsely punctured ; vertex
smooth and shining. Third joint of antennae nearly half as long
again as the fourth, antennae with more than 100 and less than
110 joints. Thorax and median segment smcoth and shining, a
few scattered punctures with a short hair springing from each on
the median segment. ‘The longest spur of the hind tibia is about
half as long as the hind metatarsus. Valvulae finely transversely
striated on the basal half. An oblique hyaline streak in the first
cubital cell extending into the angle of the second discoidal cell.
Hab. N. QUEENSLAND, Townsville (F. P. Dodd), Novem-
ber 29, 1901; Mackay (Turner), November 1892.
Described from two females.
Stigmatobracon basipennis, sp. n.
2. Very near xanthostigma, but has the terebra shorter, only 2 mm.
in length; the red colouring extends further on the abdomen,
almost reaching the middle of the third segment; and the wings
are yellow at the base for about one-sixth of their length.
Long. 14 mm.; terebrae long. 2 mm.
Hab. N. QUEENSLAND, Kuranda (Turner), May 1913.
Stigmatobracon diversipennis, sp. n.
oO
2. Rufo-testacea; capite, mesonoto lateribus postice, meso-
sterno, segmento mediano, segmentis abdominalibus quarto, quinto
sextoque, coxis, tarsis posticis intermediisque, femoribus posticis
intermediisque, apice extremo excepto, tibiis intermediis subtus,
tibiisque postica dimidio apicali nigris; alis ad nervulum flavis,
dimidio apicali fuscis, stigmate fasciaque lata sub-stigmate flavis.
Long. 14 mm.; terebrae long. 2 mm.
The antennae are a little shorter than in basipennis, being
Australian Braconidae in the British Museum. 93
scarcely as long as the whole insect, but the joints seem as
numerous.
Hab. Vicrorta (French). (Possibly from a more northern
locality.)
Stigmatobracon torresensis, sp. n.
3. Rufa; capite, abdomine, tarsisque posticis nigris; segmentis
abdominalibus duobus basalibus rufis; mandibulis palpisque testa-
ceis; alis fuscis, stigmate nigro macula parva basali flava.
Long. 10 mm. y
3. Differs from xanthostigma in the colour of the stigma.
The abdomen is more slender than in females of the genus,
the third tergite being fully as long as broad, as are also
the fourth and fifth tergites. The seventh tergite is short,
very broadly subtruncate at the apex.
Hab, QUEENSLAND, Cape York (Turner), May 1902.
Genus Bracon, Fabr.
Bracon walkeri, sp. n.
2. Rufo-testacea, nitida; capite, valvulis terebrae, unguiculisque
nigris; alis dimidio basali flavis, dimidio apicali fuscis, stigmate
maculaque magna sub stigmate flavis.
lord
Long. 7 mm.; terebrae long. 1°5 mm.
®. Smooth and shining; head transverse, distinctly narrowed
behind the eyes; scape short, ovate; antennae fully as long as the
whole insect, excluding the terebra. Parapsidal furrows distinct.
Abdomen and neuration as in B. bimaris, but the second tergite
is as long as the third and much narrowed to the base, second suture
straight in both species.
Hab. N. QueensLAND, Kuranda (Turner), June and
July; NortHerN Terrirory, Adelaide River (J. J.
Walker), August 1890.
Belongs to the group of B. wrinator, Fabr. The colour
of the wings is prevalent among the Braconidae in tropical
Australia, especially in the genera Cyanoplerus and Diso-
phrys, but 1 do not know another instance in the genus
Bracon. 7
Bracon bimaris, sp. n.
®. Rufa, nitida; capite, prothorace, valvulis terebrae, pedibusque
nigris; segmentis abdominalibus apicalibus interdum etiam nigris ;
alis venisque fuscis.
Long. 7 mm.; terebrae long. 7 mm.
94 Mr. Rowland E. Turner on
©. Smooth and shining; head transverse; antennae as long as
the whole insect, excluding the terebra; scape short, ovate. Parap-
sidal furrows distinct, but rather shallow. Abdomen as long as
the head and thorax, a little broader than the thorax, the sides
almost parallel; first tergite a little longer than its apical breadth;
second tergite shorter than the third, twice as broad at the base as
long. Radial cell reaching to the apex of the wing, the radius
originating just before the middle of the stigma; first abscissa of
the cubitus strongly bent at about one-third from the base ;
recurrent nervure received very distinctly before the first transverse
cubital nervure.
Hab. Tasmanta, Eaglehawk Neck (Turner), February.
This belongs to the group of the European B. urinator,
Fabr. The brilliant red colour renders it very conspicuous.
Genus CyANopTeRus, Hal.
KEY TO THE AUSTRALIAN SPECIES.
1. Wings yellow from the base to the
basal nervure. | 2.
Wings fuscous the stigma only yellow. C. innotatus, Turn.
2. A broad yellow band extending from
the yellow stigma almost to the
inner margin of the fore-wing . . C. profiscator, Fabr.
The stigma yellow, but without a
yellow band below the stigma. . C. rufus, Szép.
T have not seen C. crassicaudis, Szép., which belongs to
the genus, the locality of which is doubtful. C. festivus,
Szép., from New Guinea and C. levissimus, Cam., from
Tenimber also belongs to the genus. The latter is [phiaulax
levissimus, Cam. 1912 (nec Cam. 1906), and is very nearly
allied to C. profiscator, differing in the rather shallower
emargination of the apical margin of the second tergite
and in the red colour of the base of the hind metatarsus.
I do not agree with Szépligeti in including the group of
Bracon capitator, Fabr., m the genus.
Cyanopterus profiscator, Fabr.
Ichneumon profiscator, Fabr., Syst. entom., p. 335, 1775.
Bracon profiscator, Fabr., Syst. Piez., p. 105, 1804.
This species is very closely allied to C. rufus, Szép.,
Australian Braconidae in the British Museum. 95
differing in the presence of a broad yellow band which
crosses the wing below the stigma, almost reaching the
inner margin. In some specimens the hind tibiae are
black at the extreme apex, in others wholly testaceous
red. C. crassicaudis, Szép., may be a synonym, but the
description is too short for certain identification.
Hab. NortHeRN Territory, Port Darwin (J. J.
Walker); QuEENSLAND, Cape York (Turner), April and
May; Kuranda (Turner), May; Mackay (Turner), Septem-
ber to January.
Cyanopterus rufus, Szép.
I phiaulax rufus, 8zép., Termes. Fuzetek., xxiv, p. 397, 1901.
Cyanopterus rufus, Szép., Ann. Mus. Nat. Hungar., iv,
p. 586, 1906.
Hab. New Soutu Wa tes, Hunter River; QUEENSLAND,
Mackay (Turner), September, October and March.
Cyanopterus innotatus, sp. n.
9. Rufo-testacea; capite, valvulis terebrae, tarsisque posticis
nigris; alis fuscis, stigmate flavo, apice extremo fusco.
Long. 8 mm.; terebrae long. 3 mm.
Q. Scape less than twice as long as broad; face shining, closely
and minutely punctured, vertex smooth and shining. Parapsidal
furrows shallow and indistinct. Thorax and abdomen smooth
and shining; first tergite a little longer than the apical breadth,
the sides deeply grooved longitudinally; second tergite twice as
broad in the middle as long, the grooves separating the raised
anterior angles from the rest of the segment separated in the middle
of the anterior margin by a rather narrow raised space, the hind
margin of the segment widely and shallowly emarginate in the
middle. Sheath of the ovipositor thickened towards the apex.
First abscissa of the radius straight, not bent at the base.
Hab. QuEENSLAND, Kuranda (Turner), January.
Closely allied. to rufus and profiscator, but easily distin-
euished by the fuscous colour of the wings, and in the less
strong emarginate apical margin of the second tergite.
Genus IpHtaunax, Forst.
Iphiaulax transiens, sp. n
2. Flavo-testacea; capite, mesothorace, segmento mediano;
segmentis abdominalibus quinto sequentibusque, valvulis terebrae,
96 Mr. Rowland E. Turner on
coxis femoribusque posticis, tibiis posticis dimidio apicali, tarsisque
posticis apice nigris; alis dimidio basali flavis, dimidio apicali fuscis,
stigmate maculaque sub-stigmate flavis.
3. Feminae similis.
Long. 2, 8 mm.; terebrae long. 2°5 mm.; 3, 3-9 mm.
. Antennae as ‘lone as the whole insect, including the terebra;
seape less than twice as long as broad. Head smooth and shining,
the face with scattered punctures. Thorax and median segment
smooth and shining, parapsidal furrows distinct. Abdomen smooth
and shining; the first tergite scarcely longer than its apical breadth,
the raised median portion long and narrow, without carinae, the
lateral grooves almost as wide as the raised area. Second tergite
short and broad, about twice as broad at the base as long, elevated
in the middle at the base, but without a defined basal area; the
basal angles with a broad raised area which touches the elevation
in the middle of the anterior margin, and extends nearly to the
apical angles; second suture not quite straight, very feebly arched
in the middle, very delicately crenulated. Areas of the anterior
angles of the third tergite large, those of the fourth tergite smaller.
Recurrent nervure interstitial, first abscissa of the cubitus straight.
Hab. N. QuEENSLAND, Mackay (Turner), February to
May 1900; Kuranda (Turner), May and June 1913;
Nortuern Terrirory, Port Darwin (J.J. Walker), June;
N. W. Austratia, Baudin Island (J. J. Walker).
This is one of the commonest Braconidae in Northern
Austraha. It approaches Cyanopterus very closely, but
has the second suture finely crenulated, so cannot be
included in that genus as defined by Szépligeti.
Genus MAcROBRACON, Szép.
Macrobracon nobilis, sp. n.
2. Rufa; capite, mandibulis palpisque exceptis, valvulis terebrae,
tarsis posticis, unguiculisque nigris; alis dimidio basali flavis,
dimidio apicali fuscis, stigmate, cellula cubitali prima, secunda fere
tota, cellula discoidali secunda macula magna basali, cellulaque
radiella macula basali flavis.
Feminae similis; oculis maximis.
Long. 2° 3, 17 mm.; terebrae long. 6 mm.
Antennae as long as the whole insect; front opaque, rugose ;
vertex shining with very minute and sparse punctures. Mesonotum
smooth and shining, the parapsidal furrows obsolete posteriorly.
Median segment short, shining, with a few small scattered punctures.
Australian Braconidae in the British Museum. 97
Abdomen opaque, very finely rugose; second and third sutures
crenulate. First tergite short, with a longitudinal carina which
does not reach the apex; second tergite longer than the third,
broadened from the base, shorter than its apical breadth, the
median area large, not sharply defined, triangular, the apex of the
triangle touching the apical margin. First abscissa of the radius
much shorter than the second, nearly as long as the second trans-
verse cubital nervure; nervulus not quite interstitial, received a
little beyond the basal nervure.
Hab. N. QUEENSLAND, Mackay (Turner), April 1900,
May 1899, 399; Townsville (F. P. Dodd), 1 3.
Differs in the points of neuration mentioned from typical
Macrobracon, which has the second abscissa of the radius a
little shorter than the first, whereas in the present species
it is nearly half as long again. This is due to a lengthening
of the second cubital cell, and not to a shortening of the
first abscissa of the radius.
To this genus also belong Iphiaulax clavimaculatus,
Cam. and Strand (1912), from Flores, and [phiaulax fulvo-
pilosus, Cam. (1905), from Ceylon, in both of which the
second cubital cell is much longer than in the typical species
of the genus, as is also the case in Iphiaulax megaplerus,
Cam. (1905), (nec Cam. 1887) = successor, Schulz (1906),
which also belongs to the genus. I have not seen males of
any of these species.
Genus MeGaALomMum, Szép.
Megalommum annulatum, sp. n.
2. Nigra; capite thoraceque rufis ; antennis segmentoque mediano
nigris ; seg¢mento abdominali primo ventrali, tergite primo lateribus,
segmentisque 3-7 margine apicali anguste albidis; alis fusco-
hyalinis, stigmate venisque nigris.
3. Feminae similis.
Long. 2, 9 mm. ; terebrae long. 2 mm.; 3, 8 mm.
Q. Face finely rugose, not very narrow; eyes large, widely but
shallowly emarginate on the inner margin near the base of the
antennae ; front deeply hollowed between the base of the antennae
and the anterior ocellus; the vertex smooth and shining. Thorax
and median segment smooth and shining, the parapsidal furrows
almost entirely obsolete. First tergite broadened from the base,
nearly half as long again as its apical breadth, the black median
portion separated from the white lateral portions by distinct
TRANS. ENT. SOC. LOND. 1918.—PARTS I, II. (DEC:) H
98 Mr. Rowland E. Turner on
marginal carinae; second tergite broader than long, with a tri-
angular area at the middle of the basal margin, the apex of the
triangle reaching beyond the middle of the segment, the base occupy-
ing not more than half of the basal margin, the triangle margined by
a smooth groove on each side, an oblique lateral groove on each side
of the segment, second suture smooth. Third tergite with a very
small area at each of the anterior angles ; the whole abdomen smooth
and shining. First abscissa of the cubitus strongly curved near
the base ; radius originating close to the middle of the stigma.
Hab. Tasmania, Haglehawk Neck (Turner), February
1913; 8S. W. Ausrraria, Yallingup (Zurner), October to
December 1913.
The eyes are not quite as large as in typical species of
the genus, and the face is therefore broader. The tegulae
are large.
Genus Merinotus, Szép.
This genus is mainly Malayan, though several species
occur in Africa. There seems to be only one Australian
species.
Merinotus xanthocephalus, sp. n.
2. Nigra capite flavo; thorace, pedibus anticis, pedibusque
intermediis, coxis exceptis, rufis ; segmento mediano nigro, in medio
nonnunquam rufo suffuso; abdomine nigro, rufo-brunneo suffuso ;
ventre albo-flavido, lateribus nigro-maculato; alis fuscis, stigmate
fusco, venis nigris.
3g. Feminae similis.
Long. 2, 12 mm.; terebrae long. 25 mm.; 3, 10 mm.
2. Rostrum a little elongate, the palpi normal, none of the joints
broadened. Face very finely and rather closely punctured, shining ;
front and vertex smooth; a rather shallow rounded depression above
the base of the antennae. Parapsidal furrows well defined, the
median lobe of the mesonotum not prominent; thorax and median
segment smooth and shining. Abdomen rather slender; first
tergite nearly half as long again as the apical breadth, with deep
lateral furrows, the lateral margins of the segment and the margins
of the elevated median area forming carinae, the space between the
carinae shining, finely and irregularly rugulose. Second tergite
with an oblique carina on each side from near the inner side of the
basal angles, separated at the apex by about half the distance which
separates them at the base; with a small elongate triangular area
in the middle of the basal margin, from the apex of the triangle
Australian Braconidae in the British Museum. 99
a carina runs to the apex of the segment, the surface of the segment
shining, with irregular rugae; second and third sutures crenulate.
Anterior angles of the third tergite divided from the rest of the
segment by a crenulated groove, the segment with a median longi-
tudinal carina, the base longitudinally striated; the remaining
segments smooth. First abscissa of the cubitus almost straight;
the first discoidal cell much higher on the basal than on the recurrent
nervure.
Hab. NortH QurENSLAND, Mackay (Turner), October
to May; Kuranda (Turner), November.
The scheme of colouring is fairly common among the
larger Braconidae of the Austro-Malayan region and extends
to the tropical districts of Queensland. This species is
somewhat allied to palpalis, Szép., which has the third
and fourth joints of the palpi broadly flattened, and to
medianus, Szép., which has the face rugose.
I doubt if the genus Merinotus can be separated from
Sigal phogastra, Cam., which has priority; but the male of
Sigalphogastra has only five visible tergites, the fifth being
very large; in M. xanthocephalus the male shows six
tergites, the fifth very large and the sixth small. In both
the mouth parts are somewhat elongate. The female of
Sigalphogastra is still unknown. The male of the common
South African species Merinotus bellosus, Sm., has six
tergites visible, the fifth not unusually large and the sixth
not very small. Until larger collections are available it
is perhaps better not to sink the name Merinotus.
Genus CAMPYLONEURUS, Szép.
KEY TO THE AUSTRALIAN SPECIES
1. Thorax and abdomen red-brown. 2:
Thorax red, abdomen black. . . . C. mutator, Fabr.
2. Wings flavo-hyaline . . . . . . C. australiensis, Szép.
Wings fusco-hyaline. 3.
3. Stigma yellow, the apical third or
less black. 4.
Stigma black, a narrow spot in the
middle only yellow . . . . . « C. praeclarus, Turn.
4. Sixth and seventh tergites black;
tergites 3-5 finely rugose. . . . C. profugus, Turn.
Tergites wholly red-brown; tergites
3-5 almost smooth, shining. . . C. praepotens, Turn.
100 Mr. Rowland E. Turner on
1. Campyloneurus mutator, Fabr.
Ichneumon mutator, Fabr., Syst. entom., p. 335, 1775.
Bracon mutator, Fabr. ., syst. Piez., p. 109, 1804.
2. Nigra; thorace, segmento mediano, pedibusque anticis rufis ;
tibiis tarsisque intermediis fusco-ferrugineis; alis fuscis, stigmate
venisque nigris; ventre basi albido.
Long. 6-7 mm.; terebrae long. 2—2°5 mm.
°. Front very finely punctured; vertex, thorax and median seg-
ment smooth and shining; parapsidal furrows shallow. First
tergite finely rugulose ; second tergite rugulose, with a small, smooth,
triangular area at the base, which is produced at the apex into a
carina which does not quite reach the apex of the segment, an oblique
carina on each side starting from near the basal angles, and not
quite reaching the apex of the segment; the remaining tergites
finely and closely punctured. First abscissa of the cubitus sharply
bent near the base.
Hab. N. QuEENSLAND, Mackay (Turner), September and
March; Kuranda (Turner), May 1913.
Brullé wrongly identifies this species, placing it in his
genus Myosoma. IT have not been able to identify his
species, but it is certainly not the Fabrician species. Dalla
Torre, without any apparent reason, gives America as the
locality. The type of mutator is in the Banksian collection.
2. Campyloneurus australiensis, Szép.
Iphiaulax australiensis, Szép., Termes. Fuzetek., xxiv,
p- 369, 1901, 3 (nec Szép. 1905).
Campyloneurus ‘australiensis, Széep., Ann. Mus. Nat.
Hungar., iv, p. 561, 1906.
Hab. N. QUEENSLAND, Cooktown.
I have not seen this species, which appears to be closely
allied to the two following. The wings are flavo-hy aline,
the stigma yellow, and the fifth tergite of the male black.
3. Campyloneurus profugus, sp. n.
2. Rufo-castanea; capite, segmentis abdominalibus sexto septi-
moque, pedibusque nigris; tibiis tarsisque anticis ferrugineis,
intermediis posticisque fusco-ferrugineis; alis pallide fuscis, stig-
mate flavo, apice nigro, venis nigris.
Long. 8 mm.; terebrae long. 5 mm.
Australian Braconidae in the British Museum. 101
®. Face finely rugose ; vertex, thorax and median segment smooth
and shining; parapsidal furrows shallow. Raised median area of
the first tergite finely granulate, with a low median longitudinal
carina, the lateral grooves deep. Second tergite rugulose, with a
small, smooth, triangular basal area, from the apex of which a
carina extends almost to the apical margin; on either side of the
basal area is another smooth, elongate area, which is slightly oblique
and becomes narrowed and obsolete towards the apex. Second
suture crenulate; tergites 3-5 delicately rugose; the apical margin
of each slightly raised with a punctured groove before the apex.
First abscissa of the cubitus sharply bent near the base.
Hab. N. QurENsLAND, Mackay (Turner); Kuranda
(Turner), May 1913.
4. Campyloneurus praeclarus, SPs He
2. Rufo-castanea; capite nigro, orbitis hic illic angustissime
rufo-marginatis, segmentis abdominalibus sexto septimoque, pedi-
busque posticis nigris, tarsis posticis, tibiisque tarsisque intermediis
ferrugineis; alis pallide fuscis; stigmate flavo, apice costaque late
nigris; venis nigris; ventre albido, nigromaculato.
Long. 6-7 mm. ; terebrae long. 3°5-4 mm.
Very similar to profugus, but differs in the colour of the
stigma, which is broadly black on the costa; the terebra
is shorter, and tergites 3-5 are shining as in praepotlens.
The colour of the. intermediate legs is variable.
Hab. N. QUEENSLAND, Mackay (Turner), April.
The male has the median segment, partly black in some
specimens. It is possible that this will prove to be a
variety of C. profugus, the sculpture of tergites 3-5 and the
colour of the stigma showing some tendency to vary.
Campyloneurus praepotens, sp. n.
®. Rufo-castanea; capite nigro; pedibus intermediis posticisque
nigris, rufo-variegatis; alis pallide fuscis, stigmate flavo, apice
extremo nigro, venis fuscis.
Long. 9 mm.; terebrae long. 9 mm.
Very similar to C. profugus, but differs in the much
longer terebra; in the sculpture of tergites 3-5, which are
smooth and shining, punctured only in the ante- -apical
groove, and in the colour of the apical segments. The
102 Mr. Rowland E. Turner on
black spot at the apex of the stigma is also less extensive
in the present species.
Hab. N. Qurenstannd, Mackay (Turner); ‘Townsville
(Dodd).
Genus Ipopracon, Thoms.
Ipobracon ingressor, sp. n.
©. Rufa; capite flavo, antennis nigris; abdomine, tarsis inter-
mediis articulis tribus apicalibus, tibiisque tarsisque posticis nigris ;
tergitis $-8 apice angustissime albo-marginatis; sternitis albidis,
utringue nigromaculatis ; alis pallide fuscis ; stigmate venisque fuscis.
Long. 11 mm.; terebrae long. 45 mm.
©. Head rather large, not narrowed behind the eyes ; face minutely
and closely punctured, a narrow groove reaching from between the
antennae to the anterior ocellus. Scape twice as long as broad;
antennae distinctly longer than the whole insect, measuring about
13 mm. Vertex and thorax smooth and shining, the parapsidal
furrows almost obsolete. Median segment sparsely and minutely
punctured; abdomen smooth and shining; second tergite with a
large triangular basal area, which nearly reaches the apical margin,
the marginal grooves of the basal area smooth; the anterior angles
of the second tergite bounded bya smooth groove which runs from
the basal angles of the triangular area to beyond the middle of the
lateral margin of the tergite; second suture broad and finely crenu-
late in the middle, narrow and smooth at the sides. - Anterior
angles of the third tergite large, the grooves bounding them reaching
to the middle of the lateral margin of the segment, but not to the
middle of the basal margin. First abscissa of the cubitus sharply
bent at about one-third from the base, recurrent nervure received
by the first cubital cell a little before the apex; nervulus not quite
interstitial, received just beyond the basal nervure.
Hab. N. Qurenstanp, Kuranda (Turner), December
1901; Mackay (Turner), October 1899.
I took three specimens at the same time at Kuranda,
; Ms ;
flying round a fallen log in dense jungle. The Mackay
specimen is smaller measuring 19 mm., terebra 27 mm.,
but I think it belongs to the same species.
This seems to belong to the group of I. marginatus, Szép
Ipobracon pallidicolor, sp. n.
©. Rufo-testacea; antennis, valvulis terebrae, unguiculis pedi-
busque posticis nigris; capite, prothorace, pedibusque anticis
Australian Braconidae in the British Museum. 108
intermediisque flavis; alis subhyalinis, stigmate venisque fusco-
testaceis.
g. Feminae similis.
Long. 9, 7 mm.; terebrae long. 6 mm.; 3, 4-7 mm.
os
the whole insect, measuring 9 mm. in length. Face shining, indis-
tinctly punctured, with a longitudinal sulcus on the upper half;
front and vertex smooth and shining; head not narrowed behind
Scape more than twice as long as broad; antennae longer than
the eyes. Thorax and median segment smooth and_ shining;
parapsidal furrows distinct, but shallow. Raised area of the first
tergite broad, almost smooth, distinctly margined. Second tergite
with a lanceolate raised median area, which extends very narrowly
almost to the apex, a small elongate-ovate subconcave space on
each side of the area; the apical margin of the segment broadly
and shallowly emarginate, the second suture smooth, Anterior
angular areas of the third tergite small; the whole abdomen smooth
and shining. First abscissa of the cubitus bent near the base,
recurrent nervure received before the first transverse cubital
nervure; nervulus interstitial.
Hab. N. QuEENSLAND, Mackay (Turner), October 1899,
March to May 1900; Kuranda, July 1913.
The second suture is interrupted in the middle by a
narrow ridge, but there is no raised area on the third
segment,
Ipobracon quadricolor, sp. n.
2. Variegata; capite flavo; thorace pedibusque anticis rufis;
segmentis abdominalibus tribus basalibus quartoque basi ochraceis ;
antennis, mesepleuris, segmento mediano, segmentis abdominalibus
apicalibus, valvulis terebrae, pedibusque intermediis posticisque
nigris; femoribus intermediis apice tibiisque intermediis basi fusco-
ferrugineis; tergitis sexto septimoque, interdum etiam quinto, apice
angustissime albo-marginatis; alis fusco-hyalinis.
Long. 6 mm.; terebrae long. 4 mm.
®. Antennae about equal in length to the whole insect. Very
similar in structure and sculpture to /. pallidicolor; but the raised
area of the second tergite is broader, and bounded by deep smooth
grooves, not by a broader subconcave area, the raised spaces at the
basal angles are also much larger, almost extending to the basal
angles of the raised area; the lateral grooves reach the apex, which
is not the case in pallidicolor; the third tergite has a small, raised,
triangular area at the base, and the areas at the anterior angles are
arge.
104 Mr. Rowland E. Turner on
Hab. N. QUEENSLAND, Kuranda (Turner), May 1913;
Mackay (Lurner), September 1899.
Ipobracon gilberti, sp. n.
Q. Variegata; capite flavo; prothorace mesonotoque rufis ; anten-
nis, mesopleuris, mesosterno, scutello, segmento mediano, seg-
mentis abdominalibus tertio apice, quarto sequentibusque, valvulis
terebrae, pedibusque intermediis posticisque nigris; segmentis
abdominalibus primo, secundo, tertioque basi ochraceis; segmentis
4-7 dorsalibus apice angustissime albido- marginatis; femoribus
intermediis apice, tibiisque intermediis basi fusco-ferrugineis; alis
fusco-hyalinis, stigmate venisque fusco-testaceis.
Long. 11 mm.; terebrae long. 8 mm.
2. Closely allied to J. quadricolor; but is a larger species, with
the face distinctly punctured; the basal area of the second tergite
is large, forming an equilateral triangle, the grooves bounding it
indistinct, the raised areas at the basal angles large, touching the
median area at the base, the lateral grooves not reaching the apex
of the segment; the apical margin of the segment shallowly emargin-
ate in the middle. Third tergite without a raised median area,
the areas at the basal angles fairly large. Second suture smooth.
Otherwise as in quadricolor, but the recurrent nervure almost
interstitial.
Hab. N. QUEENSLAND, Mackay (Turner), October 1899;
Kuranda (Turner), November, May and July.
This species, together with pallidicolor and quadricolor,
seems to be related to the New Guinea species J. elegans,
Szép. In all these the second tergite is much broader than
long, as is usual in Australian species of the genus.
Ipobracon torridus, sp. n.
. Rufa; capite pedibusque anticis intermediisque rufo-flave-
scentibus; abdomine ochraceo; antennis, pedibus posticis, valvu-
lisque terebrae nigris; alis subhyalinis, leviter infumatis, venis
fusco-testaceis.
Long. 11 mm.; terebrae long. 8 mm.
©. Though very different in colouring I cannot find that this
differs either in sculpture or structure from J. gilberti. I do not
think, however, that it can be a mere colour variety of that species.
Hab. N. QuEENSLAND, Cape York (Turner), April 1902.
Australian Braconidae in the British Museum. 105
Ipobracon flaviceps, Cam.
Poecilobracon flaviceps, Cam., Ann. Mag. Nat. Hist. (7)
Wiad, ps 122. 1901, 2:
A variety of this occurs at Mackay. The typical form
has the tergites black, the second sometimes stained with
fusco-ferruginous; in the Mackay form the three basal
tergites at least are yellowish brown; the legs are black
in the type, but in the Mackay form the fore legs entirely
and parts of the intermediate and hind legs are testaceous
brown. The second suture in this species is straight and
crenulated. As the colour differences appear to be con-
stant, I propose for the Mackay form the name J. flaviceps
subspec. mackayensis, subspec. n.
Hab. N. QueEENSLAND, Mackay (Turner), October and
November 1899.
The locality given for the type is Australia, but it prob-
ably came from the south-eastern portion of the continent.
Ipobracon fraterculus, sp. n.
9. Nigra; capite flavo; segmentis dorsalibus duobus basalibus
ochraceis, quarto sequentibusque apice angustissime albido-
marginatis; ventre albido, nigro-maculato; tibiis tarsisque anticis
brunneo-ferrugineis; tegulis testaceis; alis fusco-hyalinis, venis
fuscis, stigmate pallide brunneo-flavescente.
Long. 10 mm.; terebrae long. 9 mm.
2. Face subopaque, minutely punctured; the antennal tubercles
prominent; front and vertex smooth and shining, a shallow depres-
sion between the anterior ocellus and the base of the antennae;
scape more than twice as long as broad, cylindrical; head not
narrowed behind the eyes. Thorax and median segment smooth
and shining; the parapsidal furrows distinct, but shallow. First
tergite smooth, longer than the apical breadth, the lateral grooves
narrow and not margined externally; the raised portion with an
indistinct median longitudinal carina and with distinct lateral
carinae. Second tergite short, broader at the base than long,
widened to the apex; the basal raised area large, triangular, mar-
gined at the sides by broad and rather shallow grooves in which
are a few oblique striae; the lateral grooves of the segment very
narrow, but extending to the apical angles; second suture almost
straight, crenulated. The areas at the anterior angles of the third
tergite are rather large. Recurrent nervure almost interstitial ;
first abscissa of the cubitus straight.
106 Mr. Rowland E. Turner on
Hab. S. W. Ausrratia, Yallingup (Lurner), October
1913.
Closely related to flaviceps, Cam., but differs in the straight
first abscissa of the cubitus, in ‘the colour of the basal
tergites, in the striation of the grooves by the median area
of the second tergite and in the very much smaller raised
areas at the anterior angles of the same tergite. The
terebra is also considerably longer.
As I have not seen several of the Australian species of
this genus deseribed by Szépligeti, [ am unable to give a
key to the species.
Subfamily AGATHINAE.
Genus Micropus.
KEY TO THE AUSTRALIAN SPECIES.
1. With a distinct longitudinal cara on
the middle lobe of the mesonotum ;
median segment with an enclosed
median area... . . . . . M.rufobrunneus, Turn,
Mesonotum without a carina; median
segment without an enclosed area. 2.
2. Median segment coarsely punctured
rugose ; antennae 27-jointed. o.
Median segment shining, almost
wholly smooth; antennae 37-
jomted ss. . % es «.s « 2 = le marialis,. Lurn,
3. Head black; thorax red. . . . . WM. rufithorax, Turn.
Head yellowish brown, with a broad
black band on the vertex; meso
thorax and scutellum black . . . M. xanthopsis, Turn.
~
I have not seen M. pedunculatus, Szép. (1905), described
from Sydney. In this species the mediellan vein is obsolete,
which is not the case in any species described here.
Microdus rufobrunneus, sp. n.
©. Rufo-brunnea; capite pedibusque intermediis posticisque
nigris; tibiis tarsisque intermediis, tibiis posticis basi, tarsisque
posticis basi et apice pallide flavis; alis subhyalinis, leviter infus-
catis, stigmate venisque brunneo-testaceis.
Long. 6 mm.; terebrae long. 4 mm,
Australian Braconidae in the British Museum. 107
®. Smooth and shining, the face closely and minutely punctured ;
antennae inserted further from each other than from the eyes,
35-jointed. Mesonotum minutely punctured, parapsidal furrows
deep and well marked, the median lobe furnished with a distinct
longitudinal carina. The sulcus at the base of the scutellum broad
and containing several longitudinal carinae; median segment with
a well-defined elongate oval enclosed median area, which is trans-
versely striated, the remainder of the dorsal surface transversely
rugulose, a patch of yellowish white pubescence on each side before
the posterior coxae. First tergite a little longer than its apical
breadth, with a few delicate longitudinal carinae on the basal half;
impressed transverse line of the second tergite arched, close to the
base at the sides; curving to the middle of the segment. Second
cubital cell triangular, petiolate; nervulus interstitial.
Hab. N. QUEENSLAND, Townsville (7. P. Dodd).
Microdus xanthopsis, sp. n.
Q. Nigra; capite, pronoto, mesopleuris antice, pedibusque anticis
flavo-testaceis; vertice fascia lata transversa antennisque nigris ;
tibiis intermediis macula subbasali, posticis basi anguste et in medio
latissime, calcaribusque albis; alis hyalinis, leviter infuscatis,
stigmate venisque fuscis.
S. Feminae similis.
Long. 4 mm.; terebrae long. 3 mm.
Q. Slender, smooth and shining; parapsidal furrows distinct but
not deep; scutellum long and narrow, with a slightly arched crenu-
lated sulcus at the base ; median segment coarsely punctured-rugose,
sparsely clothed with whitish hairs, the sides of the segment fmely
punctured. Second tergite with a distinct transverse impressed
line near the middle; the first tergite subtriangular, longer than the
apical breadth. Hind coxae and femora finely punctured, clothed
with short white hairs; valvulae sparsely clothed with very short
black hairs. Antennae 27-jointed, the third joint distinctly longer
than the fourth, longer than the scape. Second cubital cell
triangular, sometimes subpetiolate.
Hab. 8. W. Austrauia, Yallingup (Lurner), November
and December 1913.
Microdus rufithorax, sp. n.
2. Nigra; mandibulis palpisque testaceis; thorace pedibusque
anticis et intermediis rufis; segmento dorsali secundo basi, tibiisque
=
108 Mr. Rowland E. Turner on
posticis dimidio basali, prope basin nigro-annulatis, albidis; alis
pallide fusco-hyalinis, stigmate venisque fuscis.
3. Feminae similis.
Long. 4 mm.; terebrae long. 4 mm.
. Head smooth and shining, the face microscopically punctured.
Thorax shining, the parapsidal furrows distinct and fairly deep; the
transverse furrow at the base of the scutellum very feebly crenulated.
Median segment black, coarsely punctured-rugose, the sides of the
segment finely punctured. First tergite longer than its apical
breadth, very feebly rugulose in the middle; transverse line on the
second tergite very distinct. Hind femora punctured at the base.
Antennae 27-jointed. Second cubital cell triangular, distinctly
petiolate.
Hab. 8. W. Austratia, Kalamunda (Turner), March
1914; Yallingup (Turner), October 1913.
Differs from M. xanihopsis in colouring, in the longer
terebra, the deeper parapsidal furrows, the sculpture of
the first tergite and the less hairy median segment.
Microdus martialis, sp. n.
©. Rufo-testacea; antennis, articulis duobus basalibus exceptis,
nigris; tarsis “‘posticis fuscis; alis fusco-hyalinis, stigmate venisque
fuscis.
G. Femina similis.
Variat: 2g, Abdomine supra nigro.
Long. 5 mm.; terebrae long. 4 mm.
Q. Slender, smooth and shining, the face microscopically punc-
tured. Antennae 37-jointed, clothed with minute hairs. Parapsidal
furrows distinct, but rather shallow; the transverse furrow at the
base of the scutellum crenulated. Median segment shining and
almost smooth; abdomen smooth and shining, the transverse furrow
of the second tergite obsolete.
Hab. N. QUEENSLAND, Kuranda (Turner), May 1913.
The second cubital cell is petiolate.
In addition to colour differences this species is easily
distinguished from wanthopsis and rufithorax by the greater
number of antennal joints, by the almost smooth median
segment and by the absence of a transverse groove on
the second tergite.
Genus AGATHIELLA, Szép.
Agathiella, Szép., Termes. Fuzetek., xxv, p. 73, 1902.
Australian Braconidae in the British Musewm.
109
The species of this genus seem to be numerous in Australia,
especially in the southern half, and doubtless many more
species remain to be discovered. The structural differences
are usually small, and without a long series of specimens it is
rather difficult to come to definite conclusions as to the extent
of colour
variation, but where I have taken a number of
specimens | have not found any important colour varieties.
bo
vo
“I
KEY TO THE AUSTRALIAN SPECIES.
. Mesonotum, scutellum and median
segment black.
Mesonotum at least red.
Intermediate and hind legs entirely
black sen ne er ; aoe va
Intermediate legs vellowieh or red-
dish testaceous.
Hind tibiae wholly black, hind coxae
and tibiae testaceous red. Length
fos TOMO, Sag A Ae Se! i ee oe Testis
Hind tibiae with a narrow white ring
at the base. Length 5mm.
Hind legs black; scape black . . .
Hind coxae, trochanters, femora and
the scape yellow testaceous .
Median segment punctured-rugose.
Median segment smooth.
Intermediate femora wholly black,
hind tibiae black, with a narrow
white ring at the base. Length
so) geal | Boao 5d. ae on Bs
Intermediate fiers mostly or en-
tirely testaceous. Length not
exceeding 5 mm.
Hind tibiae black, with a very narrow
obscure whitish ring at the base.
Hind tibiae with the basal half white,
with a narrow black ring near the
[SEI ay OF eet ee las :
Intermediate legs w holly black
Intermediate legs not wholly black.
Intermediate legs wholly testaceous
Apex of intermediate femora and
middle of tibiae yellowish. . . .
bo
or
A, latibalteata, Cam.
o , Y r ~
A. festinala, Turn.
4.
A. ruficeps, Szép.
A. tenuissima, Turn.
6.
8.
A. maligna, Turn.
s
A. minima, Turn.
A, rugosa, Turn.
A. meridionalis, Turn.
9.
A. unimaculata, Turn.
A. tricolor, Szép.
110 Mr. Rowland E. Turner on
Agathiella latibalteata, Cam.
Agathis latibalteata, Cam., Entomologist, xxxix, p. 26, 1906.
This is an Agathiella, not a true Agathis, having the face
short and broad and no parapsidal furrows. As far as I
am aware typical Agathis does not occur in Australia.
Hab. AUSTRALIA.
Agathiella ruficeps, Szép.
Agathiella ruficeps, Szép., Ann. Mus. Nat. Hungar., in,
p. 52, 1905, ¢.
Hab. SYDNEY.
From the description this must be very near latibalteata,
but the hind tibiae are white at the base instead of wholly
black, and the intermediate legs are red, not black. It
is also a smaller species.
Agathiella tricolor, Szép.
Agathiella tricolor, Szép., Ann. Mus. Nat. Hungar., in,
p. 52, 1905, 9.
Hab. SYDNEY.
- Agathiella meridionalis, sp. n.
2. Nigra; capite, prothorace, mesothorace, femoribus anticis
dimidio apicali, tibiis tarsisque anticis rufis; segmento abdominali
primo albido, macula maxima mediana nigra supra et infra ; secundo
basi et lateribus albido, tertio angulis basalibus albido; alis pallide
fusco-hyalinis, stigmate venisque fuscis; calcaribus nigris.
Long. 5-6 mm.; terebrae long. 5-6 mm.
Variat: scutello scapoque rufis.
®. Feminae similis.
Variat : capite pedibusque anticis nigris.
2. Smooth and shining; the median segment with microscopic
punctures on the sides, but smooth on the dorsal surface; first
tergite more than half as long again as the apical breadth, shorter
in the male; second tergite as broad at the apex as long. Second
cubital cell petiolate, triangular, not very small.
Hab. TasmantaA, Mt. Wellington, 2300 ft. (Zurner),
January to April 1913.
Australian Braconidae in the British Museum. 111
Agathiella unimaculata, sp. n.
2. Rufo-testacea; segmento mediano, abdomine, antennis, pedi-
busque posticis nigris; abdomine segmentis duobus basalibus albo-
flavidis, segmento primo dorsali macula magna rotundata nigra ;
alis fusco-hyalinis, stigmate venisque brunneis.
Long. 4-5 mm.; terebrae long. 35-4 mm.
» ©. Median segment smooth and shining; first tergite about half
as long again as the apical breadth; second tergite broader than
long; hind tarsi distinctly shorter than the hind tibiae, a little
shorter in proportion than in A. maligna. Second cubital cell
triangular, the petiole short.
Hab. N. QuEENSLAND, Kuranda (Turner), May to July
1913.
The median segment is black on the dorsal surface only.
In a specimen from Sydney (P. de la Garde), January 1898,
the black is reduced to a median streak; the wings are also
paler. ;
Agathiella tenuissima, sp. n.
9. Nigra; capite, prothorace, tegulis, segmentis abdominalibus
duobus basalibus, primo basi nigro suffuso, pedibusque flavo-testa-
ceis; femoribus posticis apice, tibiis tarsisque posticis fuscis; alis
pallidissime fusco-hyalinis; stigmate venisque pallide fuscis.
Long. 5 mm.; terebrae long. 5 mm.
2. Median segment smooth and shining; abdomen very slender;
first tergite at least twice as long as the apical breadth; second
tergite longer than broad. Second cubital cell very small, the
petiole long, nervulus not interstitial, distinctly postfurcal.
Hab. Vicrorta (French).
Possibly the female of A. rwficeps, Szép., but the present
species has the scape yellowish, the flagellum brownish
beneath on the basal two-thirds, and the basal portion of
the hind legs is flavo-testaceous. Nor can the median
segment be described as “ etwas uneben.”
Agathiella festinata, sp. n.
2. Nigra; capite rufo; antennis nigris, articulis duobus basalibus
rufis ; pedibus rufo-testaceis, posticis trochanteribus, tibiis tarsisque
nigris; abdomine albo-flavido, segmentis dorsalibus primo secundo-
que macula mediana, tertio, quarto, quintoque basi nigris; tertio
angulis anticis late albo-flavidis; alis fusco-hyalinis, venis brunneo-
testaceis.
7
Long. 8 mm.; terebrae long. 7 mm.
112 Mr. Rowland EK. Turner on
2. Very similar in structure to A. maligna, differing in the sculp-
ture of the médian segment, which is smooth and shining on the
dorsal surface, with the sides very minutely punctured; in the shape
of the second tergite, which is much broader at the apex than long,
and in the slightly longer terebra.
Hab. 8S. Qurenstanp (ex coll. Turner, received from
French). ;
Agathiella maligna, sp. n.
9. Nigra; capite, thorace, pedibusque anticis rufis; antennis
segmentoque mediano nigris; segmentis abdominalibus duobus
basalibus albo-flavidis, tergitis duobus basalibus macula magna
mediana nigra; tibiis intermediis posticisque macula parva basali
albo-flavida; alis fuscis, stigmate nigro.
Long. 8 mm.; terebrae long. 6 mm.
Q. Head smooth and shining; seen from in front much broader
than long. Thorax smooth and shining, the parapsidal furrows
absent ; median segment finely punctured-rugulose, the apex smooth,
the sides of the segment very finely punctured and sparsely clothed
with short white hairs. First tergite distinctly longer than its
apical breadth; second tergite a little longer than broad, with a
rather indistinct impressed transverse line near the middle, which
curves towards the sides and becomes obsolete before reaching the
anterior angles; a slightly oblique lateral groove running from near
the anterior angles to the middle of the lateral margin. Valvulae
clothed with short delicate hairs. Second cubital cell very small,
petiolate.
Hab. 8. W. Ausrratta, Yallingup (Lwrner), November
1913.
Agathiella rugosa, sp. n.
2. Nigra; capite, vertice interdum antennisque nigris, prothorace,
mesothorace, scutello, coxisque anticis rufis; segmentis abdomina-
libus duobus ventralibus totis, dorsalibusque basi anguste albidis ;
femoribus tibiisque anticis, femoribus intermediis dimidio apicali,
tibiisque intermediis dimidio basali, basi anguste nigro-annulatis,
testaceis; tibiis posticis dimidio basali albis, nigro-annulatis; alis
pallide fusco-hyalinis, stigmate venisque fuscis; calcaribus albis.
Long. 5 mm. ; terebrae long. 5 mm.
Variat : scutello nigro.
3. Feminae similis, segmentis dorsalibus duobus basalibus albidis,
primo in medio nigro-maculato.
Long. 5 mm.
Australian Braconidae in the British Museum. 113
9. Face shining, minutely punctured, with sparse and very deli-
cate pubescence; median segment rather coarsely rugose. First
tergite nearly twice as long as the apical breadth; second tergite
as broad at the apex as long, the impressed transverse line distinct.
The male has the first tergite shorter, less than half as long again
as the apical breadth.
Hab. TAasMANtA, Eaglehawk Neck (Turner), February ;
Mt. Wellington, 2300 ft. (Turner), March 1913.
This differs from A. tricolor in the sculpture of the median
segment. The second cubital cell is very small, the petiole
long. The West Australian Microdus rufithorax closely
resembles this species, but has the parapsidal furrows
well developed and the head black.
Agathiella minima, sp. n.
2. Nigra; prothorace, mesothorace scutelloque rufis; palpis pedi-
busque anticis intermediisque testaceis; segmentis abdominalibus
duobus basalibus albo-flavidis, dorsali primo macula magna basali
nigra; tibiis posticis macula parva, obscura, basali, albida; alis
subhyalinis, costa nigra, stigmate venisque pallide brunneis.
Long. 3 mm.; terebrae long. 2 mm.
2. Smooth and shining; the median segment finely punctured-
rugose. First tergite scarcely half as long again as the apical
breadth; second tergite as broad at the apex as long, the impressed
transverse line very distinct. Calcaria of hind tibiae pale testaceous.
Second cubital cell triangular, the petiole short.
Hab. N. QUEENSLAND, Kuranda (Turner), July 1913.
It is possible that Ashmead’s genus Orgiloneura may be
founded on a species of this genus with somewhat reduced
neuration, but his description is too short for any con-
clusions to be drawn.
PLATYAGATHIS, gen. nov.
Nearly allied to Disophrys, with which it agrees in the
short broad face, in the distinct marginal carinae of the
frontal depression and in the very short terebra. It differs
from Disophrys i the very broad and somewhat flattened
abdomen, which is sessile, with the first tergite as broad
at the base, as long and somewhat broader at the apex;
the intermediate and hind-tarsal ungues are simple, the
ungues of the fore tarsi bifid. The median segment is
TRANS. ENT. SOC. LOND. 1918.—PARTS I, II. (DEC.) 1
114 Mr. Rowland E. Turner on Australian Braconidae.
hairy; the parapsidal furrows strong. The only species
known to me is
Platyagathis leaena, sp. n.
2. Nigra; capite rufo, antennis mandibulisque nigris; segmentis
dorsalibus primo, secundoque lateribus latissime, tertioque basi
lateribus, ventralibus primo secundoque in medio nigro-maculatis,
tertioque basi albis; tibiis anticis basi, tarsisque anticis fusco-
ferrugineis; alis fusco-hyalinis, venis fuscis.
Long. 7 mm.
° 3. Smooth and shining; the face very finely and closely punc-
tured; two short longitudinal carinae between the antennae as in
Disophrys. Antennae 49-jointed in both sexes, nearly as long as the
whole insect in the female, distinctly longer in the male; marginal
carinae of the frontal depression well defined, vertex smooth and
shining. Parapsidal furrows and the sulci of the mesopleurae
punctured; scutellum with a finely striated depression at the base ;
median segment short, the dorsal surface no longer than the scutel-
lum, coarsely reticulate, with six rather ill-defined longitudinal
carinae, covered with rather short whitish hairs, which partly con-
ceal the sculpture. Abdomen smooth and shining; the white lateral
bands of the two basal tergites as broad as the black median bands,
and continued more narrowly on the basal half of the third tergite.
Second cubital cell subquadrate, with the stump of a vein springing
from the second transverse cubital nervure; nervulus interstitial.
The cubital margin of the first cubital cell is open in the middle.
Hab. S. W. Ausrraita, Yallingup (Turner), January
1914.
(ald <..)
IV. On the naming of Local Races, Subspecies, Aberrations,
Seasonal Forms, etc. By Lorp Rotrscuisp, F.R.S.,
etc.
[Read February 6th, 1918. ]
In the “ Entomological News,” vol. xxvili, pp. 463-67,
Sir George Hampson has an article on “ The Determina-
tion of Generic Types in the Lepidoptera.” In the last
paragraph he protests against what he calls the “ Instp1ous
GERMAN SPECIFIC POLYNOMIAL NOMENCLATURE,” and says
it is unnecessary to name local, seasonal, sexual, poly-
morphic and other forms. Nevertheless, he proceeds to
say that when dealing with a species they must all be
DESCRIBED. He further adds that no such thing as a
“ SUBSPECIES ” exists in nature, and if the term is used,
it is only a PROOF of IGNORANCE.
These statements only prove that Sir George Hampson
has utterly failed to grasp the meaning of the term “ Sup-
SPECIES,” and also has misunderstood the main objects of
Zoological Nomenclature.
I will deal with the last question first. In my opinion
and that of the bulk of my zoological acquaintances “* Zoo-
LocicaL NomENCLATURE ” has been established to enable
the students of this branch of knowledge to communicate
their ideas in speech and writing in the most concise,
clearest and most orderly manner.
Now we all, I think, take our starting-point from
Linneeus, and he was the first to name local races, invent-
ing for them the term vaRieTAs. If this were the end of
the question, I would be the first to range myself under
the Linnean Banner, but subsequent writers have used
the term “‘ VARIETY,” ‘“‘ VARIETAS,” to mean indiscrimin-
ately local race, and individual aberration, and therefore
I and most other zoologists have determined, backed up
by the International Commission on Nomenclature, to
reject the term “ VARIETAS”’ altogether and to substitute
the term ABERRATION for an individual variation or mon-
strosity, and SUBSPECIES for LOCAL = GEOGRAPHICAL
RACE. Thus Sir George Hampson himself acknowledges,
in spite of his denial quoted above, that SUBSPECIES DO
exist in Nature, for he acknowledges the existence of
LOCAL RACES but proves himself unable to grasp that
SUBSPECIES and LOCAL RACE are one and the same thing.
TRANS. ENT. SOC. LOND. 1918.—PARTs I, II. (DEC.)
116 Lord Rothschild on Naming of Local Races, ete.
As to the point he raises that anything lower than a
“spECIBS ” should not be named, I consider it raises directly
the fundamental question of the purpose and convenience
of “ Nomenclature.”
Surely the following illustration should clinch the argu-
ment. Of the butterfly Colias fieldit there are two geogra-
phical races—one the Indo-Burmese race, which is smaller
and paler and is the typical race, and a much larger and
brighter Chinese race. Now surely it is much more concise
and comprehensive to say Colias fieldia chinensis than to
say ““ THE LARGER AND MORE BRIGHTLY-COLOURED CHINESE
RACE OF COLIAS FIELDI.”
Again, if the term Colias hyale ab. nigra is used, it is
more convenient than the sentence, ““ THE BLACK ABERRA-
TION OF COLIAS HYALE.”
It is to be regretted, I agree, that some authors, such
as Dr. Roger Verity, have been led into error in a different
direction, and have expanded the quite legitimate and
absolutely necessary trinomial nomenclature into a poly-
nomial one. But this is entirely due to their futile
attempts to arrange Zoological Nomenclature on a purely
PHYLOGENETIC basis.
The result of this is, that they take the several local
races of a widespread insect, and, thinking the phylo-
genetic relationship 1s evidenced by closer or less close
resemblance, proclaim the local races most alike in appear-
ance to be nearest in fact. Therefore they name them as
subspecies of subspecies, and so on. The truth is, that in
many cases local races at the extreme ends of the area of
a species are the closest in appearance, while the most
different races occur in between. It is therefore obvious
that two races which are nearest in appearance may be
phylogenetically ay widest apart. The only course open,
and the one we, 7.e. the majority, adopt, is, that as the
original ancestral foun and many other intermediate links
have long disappeared, to treat all local forms of one species
as ¢9- equal in value, and name them all trinomially.
The object of naming other lower categories is always
the same, viz. to facilitate their discussion; but here again,
led by several English zoologists, the naming of individual
aberrations has been carried too far, and in some cases
almost every second specimen has received a name. It
is, however, always of importance to name seasonal, dimor-
phic, and sexually polymorphic forms.
Trans. Ent. Soc. Lond., 1918, Plate III.
André, Sleigh & Anglo, Lid.
MOLIPPA SIMILLIMA g AND M. SABINA 4.
EXPLANATION OF PLaTE III.
Upper fig. Molippa simillima, D.-Jones, 3.
Lower ,, Me sabina, Wlk., 3.
EXPLANATION OF PLATE IV.
Upper fig. Molippa simillima, D.-Jones, °.
Lower ,, “3 sabina, Wlk., 9.
Trans. Ent, Soc. Lond., 1918, Plate LV.
André, Sleigh & Anglo, Lid.
MOLIPPA SIMILLIMA ° AND M. SABINA ¢.
ie
| i : ae coe a
‘sie a
en's
oy a ait -
\ rg ro - -
[ yj r a
: 7 —
1) P
( 117 )
V. Molippa simillima, D.-Jones: A Correction. By
EK. DuKINFIELD-JoNES, F.E.S.
[Read February 6th, 1918.]
Pires alii any,
In the Transactions of the Society of June 20th, 1907,
there is a short paper of mine on the remarkable resem-
blance between two species of Molippa.
T have recently discovered that the specimen I had
included amongst the M. simillima group and photographed
as such is in reality M. sabina, Wik.
I can only surmise that the unfortunate error arose from
my having accidentally placed one of the sabina pupae
in the box containing pupae of simillima, for I marked the
imagines of sabina, a, and those of simillima, b, as they
emerged, and this specimen was marked b.
My statement that the same description will serve for
both species was chiefly based upon the specimen figured
and must be modified. The principal difference is that in
M. simillima the dark postmedial line of the hind-wings
is strongly bent outwards from vein | to the inner margin,
whereas in sabina it is straight.
The accompanying plates, III and IV, show the two
species.
It is difficult in a subject of this kind to make a satisfac-
tory comparison without a long series of specimens. The
discocellular spots, for instance, are very variable in size
and shape in both species, and the very dark shade on
the inner margin of the hind-wings of M. sabina is, I find,
almosé absent in many of the specimens in the British
Museum.
EXPLANATION OF Puiates III, IV.
[See Explanations facing the PLatEs. |
TRANS. ENT. SOC. LOND, 1918,—PARTS I, , (DEC.)
Oatye. =)
VI. On Mimicry in certain Butterflies of New Guinea.
By EF) Ay Dixry,, M-A., MD ERS.
[Read March 6th, 1918.]
In Seitz’s “ Macrolepidoptera ” (Indo-Australian Region ;
English Edition, p. 147) under the genus Huphina, Fruh-
storfer speaks of abnormis, Wall., “ euryxanthe,’ Honr.,
and ‘* ornythion,’ Godm. & Salv., as related species. This
passage contains two minor inaccuracies and one distinct
error. Honrath’s insect was named by him euryxantha..
Oberthiir afterwards spelt the name with a final e, nm which
he ae ee followed by other authors. Staudinger, how-
ever, in “Iris,” and Grose Smith and Kirby in their
4 ral Grelnget Exotica ” rightly give the original spelling.
The second inaccuracy is in the name “ ornythion, * which
was written by its authors ornytion.
These are trivial matters; of greater importance is the
statement of affinity between ornytion and the other two
species. Though it bears so striking a resemblance to
Huphina abnornus, the relationship of ornytion to that
butterfly is not close, for it belongs in fact, as shown by
structural characters, to the very distinct genus Delias.
Much confusion has prevailed with regard to all three
butterflies now named, and it may be worth while to
attempt to clear this up before proceeding to the actual
subject of my paper.
In his well-known memoir on the Eastern Pieridae,
published in 1867, Mr. Wallace described and figured under
the name of Tachyris abnermis a remarkable Pierine from
New Guinea.* He observes that in coloration “it bears
a striking general resemblance to the beautiful nvm-
phalideous butterfly, Mynes Geoffroy, which inhabits the
same country.” The type specimen, which may still be
seen in the National Collection, is a female; if Wallace
had been acquainted with the male, he could scarcely have
avoided noting that it does not possess the anal tuft of
hairs which characterises the genus fe But the
* Trans. Ent. Soc. Lond., Series III, vol. iv, p. 368; Pl. VIII,
fig. 5, 9.
TRANS. ENT. SOC. LOND. 1918,—PARTS I, I. (DEC.)
Dr. F. A. Dixey on Mimicry in certain Butterflies. 119
general appearance of his specimen seemed to him to
indicate that it came nearest to such forms as ada. Cram.,
and claves, Wall., and he therefore placed it tentatively in
his genus Tachyris next after those species. In 1889
Messrs. Grose Smith and Kirby * figured both the upper
and under side of the same form; Wallace's figure only
showing the latter. On the plate in ‘“ Rhopalocera
Exotica” the species appears under Wallace’s name of
Lachyris abnormis, but in the text and indices its genus is
given as Delias. The figure is said to represent a male,
but is really (like Wallace’s) that of a female. The mistake
as to sex was alterwards corrected by the authors.t In the
same work, vol. 1, Pierinae, p. 17, abnormis is once more
referred to the genus Delias, and is said to belong to the
group of D. ladas, Grose Smith, and D. ornytion, Godm. &
Salv. But in the note (/bid., p. 22) cited above, the authors
add, ““ Herr von Mitis points out (‘Ivis,’ vi, p. 114),
that the four-branched subcostal nervure removes both
Abnormis and Huryxantha from Delias.’ This is quite
true; and euryxantha, which appears in the plate (“ Rhop.
Kxot.,” vol. u, Pierinae ; Delias, vi, figs. 7, 8) as a Delias,
is in the text called a Tachyris.
Honrath,t who described euryrantha as a variety of
abnormis, expressed a doubt as to whether Grose Smith
and Kirby’s figure of abnormis represented a male as stated :
he adds, however, that those authors in their text rightly
placed abnornis in the genus Delias, “to which genus,
instead of to Tachyris, Wallace, if he had known the male,
would certainly have also assigned it.’’ Staudinger §
definitely pronounced Smith and Kirby’s figure to be that
of a female.
As a matter of fact, neither abnormis nor euryxantha
is either a Delias or a Tachyris. So far as I am aware, the
first author to perceive their true affinity was von Mitis,||
who, as above stated, pointed out that their neuration
was not that of Delias. Von Mitis himself places them in
the neighbourhood of judith, amalia, emma, ete.; 7. e. in
the group named by Moore Huphina, though ranked by
the former writer under the wide designation of Pieris,
* “ Rhopal. Exot.,” vol. i, Pierinae, Pl. II, figs. 6, 7.
t Ibid. vol, ii, Pierinae, p. 22, note.
{ Berl. Entom. Zeitschr., xxxvi, p. 435 (1892).
§ “Iris,” vii, pp. 117, 118 (1894).
|| Ibid. vi, pp. 113, 114 (1893),
120 Dr. F. A. Dixey on
While there is little doubt that abnormis and euryaantha
are best referred to Huphina, it is also true that they appear
to stand somewhat apart from other members of that genus.
The genitalia of both species are of the Huphina type, but
the valves differ slightly in shape from those of H. agnata,
Gr. Smith, and H. nerissa, Fabr. The genitalia in Delias
are quite different. The scent-scales of H.. abnormis
esis easily be distinguished from those of HZ. ewryxantha,
indeed, they can be distinguished at all. They are of
re Huphina type, though shorter and proportionately
broader towards the apex than those of other species of
the genus. The difference in neuration between Huphina
and Delias is well known. The neuration of abnormis and
enryxantha is that of the former genus. Von Mitis agrees
with Honrath in attributing W allace’s mistake to the fact
that he was only acquainted with the female. Staudinger *
speaks of von Mitis as having shown that abnormis and
euryxantha belong to the genus “ Pieris (or Appias)”’ ;
but these forms have certainly no more to do with “ Ap-
pias”? than they have with Tachyris, nor did von Mitis
suggest the contrary,
As already stated, there is little or no doubt that abnormis
and euryxantha, whether they are distinct species, or
whether, as thought by Honrath, von Mitis and Staudinger,
forms of the same species, have their true affinity with the
Pierines included in Moore’s genus Huphina. This was
correctly recognised by Mr. A. G. Butler + in his Revision
of that genus. But while rightly placing them in Huphina,
to which group they almost certainly belong, he associates
with them in the same genus ladas, ornytion and doherty),
adding the following comment: ** I must confess that the
fact of the last five species occurring together in New
Guinea, in conjunction with the fact that similarly coloured
species of the Nymphalid genus Mynes occur there, is very
suspicious. | cannot help thinking that breeding experi-
ments would tend greatly to reduce the number of these
‘species > in both genera.” Mr. Butler’s suspicions that
something was wrong were well founded; and it is quite
probable that breeding experiments would show that
abnormis and euryxantha are conspecific, as was supposed
by Honrath, Staudinger and others. But along with
‘ Tris,” vii, pp. 117, 118 (1894).
+ Ann. Mag. Nat. Hist., 7th Series, vol. iii, p. 206 (1899). It
may be noted that Mr. Butler’s reference to Oberthiir’s “* Etudes ”
should be to p. 6, not to p, 61,
Mimicry in certain Butterflies of New Guinea. 121
a possible reduction in the number of species, what is really
required in the five forms associated in the “ Revision ”
is an increase in the number of genera. The first two forms
of the five, viz. ewryxantha and abnormis, belong, as we have
seen, to Huphina; but ladas and ornytion are certainly
members of the genus Delias. With regard to the fifth
species, viz. doherty:, there is a fresh complication. A
Pieris dohertyi from Jobi and a Delias dohertyi from Timor
were both described in 1894, the former by M. Oberthiir,
the latter by Lord Rothschild. Oberthiir’s description
having been published in August, and Rothschild’s in
September, it would seem that the former has priority. I
have never seen Oberthiir’s type, but from the description
and figure I have no doubt that it isa Delias. Rothschild’s
doherty is certainly a Delias, and quite distinct from
Oberthiir’s. In his Revision of the genus Delias,*
Mr. Butler refers under D. doherty’ to Rothschild’s descrip-
tion above mentioned, and also to Grose Smith and Kirby’s
figures in “ Rhopal. Exot.,” ii, Delias, Pl. IV MotB
as Butler), figs. 7, 8, which represent Rothschild’s type.
He adds, “* It is a curious thing that in the same year when
the above was described M. Oberthiir described a Pieris
Doherty: from New Guinea. The latter, however, appears
to me to be allied to P. ornytion of Godman and Salvin,
in which case it is not a Delias (although P. ornytion has
erroneously been referred to this genus by von Mitis).”
But, as we have seen, ornytion is a Delias, and if Mr. Butler
is right, as I believe he is, in thinking that Oberthiir’s
dohertyi is atlied to ornytion (of which species it seems to
be the representative in the Island of Jobi), we have two
dohertyy in the same genus, Oberthiir’s being apparently
the one that is entitled to stand; unless indeed Oberthiir’s
dohertyr should turn out to be a mere synonym of ornytion ;
in which case I presume that Rothschild’s would stand as
the true doherty. This, however, is a question that [ would
fain leave in the hands of experts in nomenclature.
Turning now to Fruhstorfer’s treatment of these forms,
we find that he ends his account of Huphina with the same
five species as those to which Butler called attention in the
passage aboye quoted, adding to them “ persephone,
Staud, (= odyssia, Frust. 7.1.).” + His notice of this
* Ann, Mag. Nat. Hist., 6th Series, vol. xx, p. 153 (1897).
+ Seitz, ‘‘ Macrolepidoptera ” (Indo-Australian Region), Engl.
Ed., p. 147,
122 Dr. F. A. Dixey on
assemblage is no doubt based on the “ Revision’; * and
we have already seen that three of its members, viz.
ornylion, iadas and doherty: belong not to Huphina but to
Delias. There remains persephone, Staud., from Waigiou.
This form, as Fruhstorfer says, “ was formerly only known
in one defective male specimen, and described as Delvas.”
His figure, which appears in loc. cit., Pl. 63d, as Huphina
odyssia, is indistinguishable from specimens of ornylion
from the Arfak Mountains in N.W. and from Kapaur in
W. New Guinea, on the underside of which forms the sub-
marginal red ine of the hind-wing is wanting, and the
Vv ellowish patch on the apex of the ‘fore- -wing may also be
absent, as in the figure of ‘“ odyssia.” Staudinger + was
no doubt right in placing persephone in the genus Delias ;
there was also some justification for his surmise that a
larger number of specimens, perhaps from other localities,
might show that persephone is a local form of ornytion.
As we have seen, there is no assignable difference between
the Waigiou form and specimens of D. ornytion from
Western New Guinea. Staudinger speaks of ornylion
as from 8.W. New Guinea, but Godman and Salvin’s
specimens, including the type, were taken near Port
Moresby. Even in “these the submarginal red line was
almost obsolete; in another specimen from Port Moresby
it is entirely lacking, as in the Cee of persephone.
We may sum up as follows >
Abnormis is not a Tachyris (as Wallace, and Grose Smith
and Kirby in their plate); nora Delias (as Grose Smith and
Kirby in their text and indices, also Honrath); nor a
~ Pieris (Appias) ” (as Staudinger); but a Huphina (as
von Mitis,t Butler and Fruhstorfer).
Euryxantha (not euryxanthe) is not a Delias (as Honrath
in his description and Grose Smith and Kirby in their
plate §); nor a Tachyris (as the two iatter authors in their
text and indices); nora“ Pieris (Appias) ” (as Staudinger) ;
but a Huphina (as von Mitis, Butler and Fruhstorfer).
It may probably be conspecific with abnormas.
* The reference to Oberthiir’s Etudes, “pb. 6L” (instead of p. 6),
above noted in the ‘* Revision,”’ is repeated in Fruhstorfer’s Alpha-
betical List of Indo-Australian Pierines; loc. cit., p. 185.
j= nis,” svily, ps 300) (L895):
t He calls it Pieris, but is aware of its true affinities.
§ Both abnormis and euryxantha are also assigned to Delias by
Grose Smith in Novit. Zool,, i, pp. 334, 835 (1894).
Mimicry in certain Butterflies of New Guinea. 123
Ornytion (not ornythion), described as a Pieris, is not a
Huphina (as Butler and Fruhstorfer); but a Delias (as
Staudinger, von Mitis, and Grose Smith and Kirby).
Persephone is not a Huphina (as Fruhstorfer); but a
Delias (as Staudinger).
Dohertyr, Oberth., described as a Pieris, is not a Huphina
(as Butler and Fruhstorfer); but a Delias. The three last-
named forms are very probably conspecific.
Dohertyi, Roths., is rightly assigned to Delias by its
describer, by Groce Smith and Kirby, and also by Butler.
Ladas is not a Huphina (as Butler and Fruhstorfer) ;
but a Delias (as Grose Smith and Kirby).
The confusion that has prevailed with regard to these
species affords a good illustration of the way in which even
skilled entomologists may be misled as to affinity by
striking resemblances in colour and pattern. It is surely
not unreasonable to suppose that analogous mistakes may
be made by insectivorous enemies.
To turn now to the main subject of this paper. It will
be observed that all the forms that have been mentioned
are inhabitants of New Guinea and adjacent islands;
also that, leaving Huphina euryxantha and the form of
Mynes geoffroyi with a light hind-wing out of account, the
remainder are characterised by a uniform dark coloration
of the under surface of the hind-wing, in some cases relieved
by streaks, touches or lines of bright red. The butterflies
in question belong to three different genera; two of the
genera, Viz. Delias and Huphina, being included in the
subfamily Prerinae, and the third, viz. Mynes, in the sub-
family Nymphalinae. Of all these forms, Delias ornytion
may perhaps be regarded as the most characteristic. I
am not acquainted with the habits and postures of any of
the members of this assemblage ; but if D. ornytion behaves
hike most other Pierines, its attitude while feeding or
resting during the intervals of flight would show on the
underside a striking contrast between the dark hind- -wing
and apex of fore-wing on the one hand, and the white
portion of the fore-wing on the other. The appearance of
the butterfly, already conspicuous and distinctive, would
be rendered still more so by the red costal streak and red
patches or submarginal line of the hind-wing. Huphina
abnormis under similar conditions would ‘display the
124 Dr. F. A. Dixey on
like contrast between white, blackish brown and scarlet,
though here it is interesting to observe that on a close
comparison the scarlet streak in abnormis is seen to be not,
as in ornytion, on the costa of the hind-wing, but on that
of the fore-wing. The thin scarlet submarginal line, often
present in ornytion, is also absent from abnormis, though a
suggestion of it may occur in the form of a few scarlet
patches, Mynes geoffroyi, or rather the form doryca,
would present, as was observed by Wallace, the same
general appearance as abnormis, the contrasting colours
being very nearly the same. But here the relative position
of the scarlet touches 1s again somewhat different. Com-
paring doryca with abnormis, we see a rough correspondence
between the scarlet costal streak on the hind-wing of the
former and that on the fore-wing of the latter: also
between the scarlet submarginal spot on the hind-wing of
the latter and that on the fore- -wing of the former. As in
abnormis, so in doryca, the hind-wing has no scarlet sub-
marginal line. The apex of the fore- -wing is in doryca
diversified with certain light-coloured marks; these are
absent from abnormis, but many specimens of ornytion
show a paler area, much less conspicuous than in doryca,
but in the corresponding situation.
If these insects, after the usual manner of butterflies,
depress the fore-wings during the periods of protracted
rest, so as to conceal the white portion of the fore-wing
and leave visible only the apex of the fore-wing and the
whole expanse of the hind-wing, the resemblance between
them becomes perhaps even more detailed. The costal
and submarginal red marks fall more nearly into their right
relative positions, irrespective of their situation on fore-
or hind-wing; and the assemblage is now joined by another
Delias from New Guinea, viz. D. irma, Fruhst. In the
male of this butterfly the under surface of both wings 1s
black, with the exception of a scarlet patch on the costa
of the hind-wing, lke that of D. ornytion, but somewhat
shorter in proportion ; there may also be a powdering
of orange-yellow scales about the distal end of the cell
in the fore- -wing, though this is often evanescent or
absent.
It is difficult to see how the facts with regard to these
four insects can be interpreted without recourse to the
theory of mimicry. The resemblance between two of them,
as has been seen, has been sufficient to cause great con-
Mimicry in certain Butterflies of New Guinea. 125
fusion, even on the part of skilled entomologists; and it is
hardly necessary to point out the improbability of this
striking resemblance between insects differing in affinity,
but all inhabiting the same region, being due to simple
coincidence. Nor, again, is it easy to suppose any factor
in the climate or external conditions of New Guinea which
could lead directly, on the part of three or four of its butter-
flies, to the assumption of a dark underside with red
markings; these markings, be it observed, belonging in
some cases to the fore-wing, in others to the hind-wing, but
always contributing to the same general effect. Whether
the explanation founded on mimicry is adequate, can
only be finally decided by observation and experiment ;
at present I think it must be admitted to hold the
field.
The scarlet markings on the hind-wing underside of
Delias ornytion would seem to be an attenuated version of
the subcostal red patch and submarginal red band seen
in the corresponding position on the hind-wing of Delias
harpalyce, Donovy., and Delias nigrina, Fabr. This series
of markings has a wide distribution among the species of
Delias, being more or less completely represented in such
species as D. aganippe, Donov. (Australia); D. kwmmerc,
tibbe, iltis, Ribbe, and bakeri, Kenr. (New Guinea) ;
D. mysis, Fabr. (Australia); D. argenthona, Fabr. (Aus-
tralia); D. caeneus, Linn. (Moluccas); D. eucharis, Drury
(India); D. stolli, Butl. (China); D. ewmolpe, Gr. Smith
(Borneo). A comparison of these and other forms appears
to favour the conclusion that in D. ornytion we have the
red submarginal series in an obsolescent rather than in
an incipient stage; and it is observable that although the
subcostal scarlet patch is persistent throughout the whole
range of this species, the submarginal scarlet line, which 1s
nearly always present in specimens from Hastern New
Guinea, and is well marked in a specimen from the Louisiade
Archipelago, has, in all the examples known to me from
Western New Guinea and the adjacent islands, completely
vanished without leaving a trace. Now it is to be remarked
that the failure of the red line in D. ornytion brings its
underside, with closed wings, into relation with that of
Delias inferna, Butl. (or as Fruhstorfer calls it when it
occurs in New Guinea, D. drma). On the mimetic-hypo-
thesis, it would be natural to ask whether the darkening
of inferna has been influenced by ornytion, and the loss of
126 Dr. F. A. Dixey on
red in ornytion by the condition in inferna. No doubt
much remains to be discovered about the distribution of
these forms in New Guinea, which is a very large country.
- But as far as is known at present, the disappearance of the
red line of D. ornytion in the western part of its area cannot
be connected with the presence of D. inferna or “wma,”
for the latter form appears not to occur in the western half
of the island. On the other hand, it would seem to be not
impossible that the dark coloration of cnferna as compared
with the other members of the aruna group may have been
influenced by ornyiion; for the only region ‘outside the
range of the latter where inferna occurs appears to be the
northern extremity of the Cape York peninsula.
It is doubtful whether any geographical relation can be
traced in the case of the red spots of Huphina abnormis.
The submarginal series of the hind-wing occurs 1m greater
or less development in specimens from Eastern New
Guinea, the first at least of the series being apparently
always present. The type, which is entirely destitute of
the hind-wing series, is said by Wallace to have come
from “ N.W. Papua’; but the present data are obviously
insufficient for forming any conclusion on this head. Nor,
again, can it be said that Ls doryca, Which is senerally
distributed throughout New Guinea, shows any difference
in the development of its red spots in correspondence with
locality.
The facts that can be affirmed with certainty are that
these four forms, viz. Delias ornytion, D. irma, Huphina
abnormis and Mynes doryca, all resemble each other, and
depart from most of their congeners, in the possession of a
dark, almost black under- Sumiace to the hind-wing, on which
occurs a series of red markings in a greater or less state
of development; that in two of them (Mynes and Huphina)
the red series is divided between fore- and hind-wing, but
presents the same general appearance as in the two Delias
in which it is to be seen on the hind-wing alone; and that
in one of the four (D. ima) the under-surface of the fore-
as well as of the hind-wing is dark, so that in the other
three the attitude of complete rest (fore-wings depressed
between hind-wings) must be adopted in order to produce
resemblance to the first. Whether these facts are open
to an interpretation on the basis of the theory of mimicry
is a question which will be answered in different senses
by different authorities; but to those who admit the
Mimicry in certain Butterflies of New Guinea. 127
validity of the theory in any form, it will seem probable
that some mimetic influence at any rate has here been at
work, though it may not be possible to determine its exact
extent.
We have seen that there is little doubt that the markings
on the hind-wing underside of D. aganippe are generally
homologous with those in the corresponding situation of
D. nigrina; and equally little doubt that the scarlet
markings of D. ornytion are an attenuated version of the
subcostal patch and red band or chain of spots seen in the
two former and many other species of Delias, especially
those belonging to what may be called the ewcharis section
of that genus. In Trans. Ent. Soc. Lond., 1894, pp. 300,
301, and Proc. Ent. Soc. Lond., 1909, p. cxi, reasons were
given, on the combined evidence of wing-markings and
scent-seales, for supposing that the eucharis section is a
natural group distinct from the belisama section, though no
doubt at one time linked with it through a form more or
less resembling Delias aganippe. D. inferna, which is a
local race of D. aruna, Boisd., is shown by both kinds of
evidence to be closely akin to belisama, and so to belong
to an assemblage in which the red subcostal patch 1s nearly
always present, and the red submarginal chain is as a rule
not to be found.* It was therefore rather to be expected,
on the theory of a mutual approach between D. inferna
and D. ornytion, that the latter should be more apt to lose
the already attenuated submarginal line than the former
to revive it or start it afresh.
Two other points of interest in connection with this
assemblage remain to be noticed.
(1) With regard to Mynes doryca it is to be remarked
that not only does the underside recall in a striking manner
the appearance of Delias ornytion and Huphina abnormis,
but its upperside also is of a Pierine rather than of a
Nvmphaline character. On a superficial view there is
little to distinguish it from the female of D. ornytion or of
H. abnormas, and the same applies to the probably con-
specific form, M. geoffroyi. The facies is the not unusual
Pierine arrangement of a pale area surrounded by a dark
border, broader in the Pierine female than in the male.
* Tt is, so far as I am aware, only present among Delias of the
belisama group in D. ewmolpe, Gr. Smith, from North Borneo and
D. funerea, Roths., from Halmaheira.
128 Dr. F. A. Dixey on
It is further remarkable that the same aspect is shared on
the BpDE Tarte by the male of Nepheronia (Pareronia of
Bingham) jobaea, Boisd., the ae of its genus in
Ceram, Bouru, Western New Guinea and the adjacent
islands. It is well known that the females of N epheronia
are mimics of other butterflies, chiefly Danaines and
Papilionines, that inhabit the same regions. The males,
however, are not usually considered to be mimetic, with the
exception péthaps of N. tritaea, Feld., of Celebes, NV.
argolis, Feld., of the Moluccas, and N. phocaea, Feld., of
the Philippines. But the contrast between the uniformly-
tinted ground-colour of NV. jobaea 3 and the black veiming
of the upper surface of the male Nepheronias from further
west, such as NV. hippia, Fabr., and pingasa, Moore (main-
land), naraka, Moore (Andamans), valeria, Cram. (Java and
Sumatra), boebera, Eschsch. (Philippines), is so striking as
to suggest the possibility that this Nepheronia has been
influenced in a mimetic direction by the New Guinea
assemblage now under discussion. As between the
Nepheronia and the Mynes, the correspondence is specially
close, for it extends even to the tint of the pale area of the
wing, which in neither butterfly is pure white. In both
species the dise of the hind-wing is pale greyish blue; and
that of the fore-wing is pale greenish yellow i in the Mynes,
and either that or very. pale. blue in the Nepheronia. It
may also be remarked that the underside of NV. jobaea 3,
by its dark hind-wing, does to some extent recall the under-
side of M. doryca, D. ornytion and H. abnormis, though it
is entirely devoid of red spots or streaks. This feature of
the hind-wing is exceptional in Nepheronia, though some
approach to it is visible in N. argolis. A somewhat similar
underside to that of NV. jobaea 3 is seen in Delias ladas,
Gr. Smith, the range, however, of the latter insect appears
to lie outside of the region inhabited by N. jobaea.
(2) It was mentioned above that Huphina abnormis and
H., euryxantha are believed by some good authorities to be
conspecific. Whether this be so or not, there is no doubt
that the two forms are at least very closely allied. Hach
possesses an underside which presents a type of coloration
very different from that which is usual in the genus; and
it is interesting to remark that while H. abnormis bears a
strong resemblance to one Delias, viz. D. ornytion, the very
different underside of H. euryxantha at once recalls the
Delias forms of the mysis group, particularly D. lara,
Minicry in certain Butterflies of New Guinea. 129
Boisd., which, like ewryxantha itself, is an inhabitant of
New Guinea.
It is obvious that with regard to all these forms much
remains to be learned concerning their relative frequency,
their exact distribution and local variation, their modes
of flight and postures during rest, and the extent to which
they are the prey of insectivorous birds or other enemies.
Only when more data are forthcoming on these heads will
it be possible to pronounce with any approach to con-
fidence on their respective bionomic relations.
My thanks are due to Lord Rothschild, F.R.S., for
personal help in examining the collections at Tring; and
to Dr. Eltringham for his skilful preparations of the
genitalia mentioned on p. 120.
TRANS. ENT. SOC. LOND. 1918.—PARTS I, II. (DEC.) K
PAs 0me)
VIT. An Instance of Mutation : Coccus viridis, Green, a
Mutant from Pulvinaria psidii, Maskell. By Be
Kunut Kannan, M.A., F.E.S.
[Read March 6th, 1918.]
Prates V—VIII.
SUMMARY.
Coccus viridis, Green, has seven segments ‘in the an-
tennae. This was so in the Mysore specimens when the
pest first appeared in the State in 1912. But specimens
collected in 1913 and afterwards, though undoubtedly
C. viridis in other respects, showed in the antennae a
reduction to three segments by the coalescence of the
terminal five into one. This indicated an instability in
the species, which has now been placed beyond a doubt
by the fact that there are in Java, besides the typical
C. viridis, two distinct types, with very variable but
usually eight antennal segments, highly unstable and with
a host of antemmediate forms. A new form from Uganda,
described first as a subspecies, has been recently given
specific rank by Newstead. C. viridis is therefore clearly
unstable.
Pulvinaria psidii is also very variable in size, antennae,
and anal plates, and some variations distinctly recall those
of C. viridis. The chief distinguishing feature, of the
secretion of meal for oviposition, may also be absent.
P. psidvi has, moreover, at least two subspecies. The gap
between P. psidvi and C. viridis being bridged over by the
variations in both these, involving the same structures,
and being in the same direction, P. psidii is the mutating
species, CU. viridis and its variants being derived directly
or indirectly.
Similar relations between species in Coccidae have been
noticed by others, and are best explained by the theory
of Mutation applied as above. An exact parallel to the
phenomenon, which occurred in C. viridis, has been noticed
by Green in Phenacoccus mangiferae. The relations de-
scribed by Quayle, of the University of California, between
Coccus citricola and C. hesperidum axe also similar to
TRANS. ENT. SOC. LOND. 1918.—PARTS I, II. (DEC.)
Mr. K. Kunhi Kannan on An Instance of Mutation. 131
those between P. psidw and ‘C. viridis, and are similarly
explained by the theory of regressive mutation.
The two insects dealt with in this paper belong to two
closely allied genera in the order Coccidae. They are flat,
oval scale or scab-like bugs, which are provided with
hair-like tubes for feeding on plant sap. The adults show
little trace of segmentation. They have three pairs of
legs, a pair of segmented antennae, a pair of eyes, and two
pairs of spiracles, which are situated a little distance
from the margin, but are connected with it by shallow
-grooves called stigmatic clefts. At the place where the
grooves touch the margin there are three stout spines, of
which the central spine is twice the size of the other two.
At short intervals along the entire margin, there are smaller
spines which are dilated or toothed at the extremity.
The anus is about a sixth of the distance from the margin,
and is guarded by two triangular chitinous plates known
as the anal plates, which hft up and open apart when there
is a discharge. From the anus, in a line with the opening
of the plates, there runs to the margin, a cleft dividing
the posterior end into two lobes. The chitin of the dorsum
has a definite pattern made up of what are called dermal
cells, which are depressions or pits * of different shapes
varying from irregularly oval to round. Coccus viridis
is viviparous, the eggs developing inside the body and
hatching usually at éhe time of discharge. Pulvinaria
psidiz, on the other hand, secretes a cottony waxy stuff
to lay eges in.
Coccus “viridis, or green bug, is a serious pest of Coffee,
which appeared in Ceylon so far back as 1882, and had no
small share in the destruction of Coffee there. It has
since appeared in the Pulneys, the Shevroys, the Nilegris,
and finally in Mysore and Coorg. It feeds on a large
number of plants, besides Coffee, viz. Tea, Guava, Citrus
plants, Cinchona, several species of Manihot, Gardenia,
Ixora, Plumiera, Eugenia, Loranthus, Antidesma, and
several varieties of garden shrubs.
* The dermal cells cannot be correctly described as ‘‘ depre ssions
or pits.’ They are actual cells in the chitinous substance of the
derm, each cell communicating with the surface by a minute pore.
They have no connection with the superficial depressions (usually
of a more or less polygonal form) that may be observed on the
dorsum of the living insect.—E. E. G.
132 Mr. K. Kunhi Kannan on
Pulvinaria psidii is known popularly as the “ mealy
bug” * for the reason already mentioned, that it secretes
a large quantity of waxy substance which appears like
cotton and forms a sort of cushion beneath the abdomen
of the insect, lifting it up and bringing it at an angle to
the surface of the leaf. The eggs are laid in this mass.
Like green bug, it 1s quite at home on a variety of plants,
viz. Coffee, Tea, Cinchona, Citrus plants, Eugenia, Guava,
Myrtle, Ficus, Cardamom, Duranta, Garcinia, Antidesma,
Alpinia, and numerous other plants.
Both these species have been studied in the Kntomo-
logical Section of the Department of Agriculture in Mysore,
ever since Coccus viridis appeared as a pest in the State
in 1912, and this paper attempts to give some of the results
of the investigation and their explanation.
When the “pest first appeared, a number of planters
sent in specimens for identification. All these were deter-
mined as Coccus viridis, as they answered in all respects
to the description of the species given by Green in his
book ** The Coccidae of Ceylon.” About a year afterwards,
when specimens happened to be microscopically examined
again, a remarkable change had appeared. The antennae,
which are seven-segmented in the species, showed a reduc-
tion to three by the coalescence of the five apical segments
into,one. Several hundreds of specimens from all parts
of the State were then examined, but none with seven-
segmented antennae were found. From one estate,
however, from which specimens were obtained immediately
on the outbreak of the pest there in 1913, a few bugs were
obtained which showed four or five segments in the an-
tennae (PI. VII, fig. 4, drawing i). Specimens from the
Pulneys, Shevroys, ‘the Nilgiris, ‘and Coorg have also been
examined, and all show a reduction to three segments,
though in some there are traces of additional segmentation.
There is little doubt, therefore, that in South India the
three-segmented condition of the antennae is practically
universal, though there is one important exception to
which reference will be made later.
The reduction may make it appear probable that the
bugs originally identified by Dr. Coleman and myself were
not the same as the bug described by Green. Since,
* Pulvinaria psidii may be locally known as “mealy bug” in
Southern India; but that term is more usually applied to members
of the genus Pseudococcus and its allies.—E. E. G.
An Instance of Mutation. 133
however, a seven-segmented antenna is one of the specific
characters relied on by Green, a reduction had it occurred
then would not have passed unnoticed. Moreover, a
photograph of one of these earlier specimens fortunately
shows seven distinct segments (PI. V, fig. 1). There is
hittle doubt, therefore, that the present form is derived
from the typical Coccus viridis.
The reduction is not a character acquired by the adult,
but appears in nymphs just hatched. This is remarkable,
since Green mentions as a characteristic of not only the
genus Lecanium (Coccus) but of all the genera in the family
that the nvmphs have s1x- -seomented antennae, and a
regards Lecanium (Coccus), he says, ‘the facts seem
to indicate a primitive six-jointed antenna.” Maskell,
another authority, considers that six is the normal number
of segments: in all Coecids. The number six in the voung
persists in the adult, or is increased by a few more, but
is seldom reduced.
Save for the inherited degeneration in the antennae,
the Mysore form is identical with the bug from Ceylon in
all microscopical details. The Ceylon specimens, obtained
recently, are smaller in size. It is also probable that
their reproductive powers are limited. Green says the
bug produces only about 20,* whereas in Mysore the number
has reached over 500. But these are minor details which
do not affect the structural identity of the two forms
except as regards the antennae.
Closely allied to the Ceylon form in sex, colour, and
antennae, specimens were obtained from one citrus plant
in Bangalore in May 1916. Periodical examination of
specimens from this plant have been made since, and so
far the reduction to three has not yet appeared, though
there seems to be a tendency for the third and fourth,
and fifth and sixth to coalesce. These specimens are
therefore the typical Coccus viridis of Green. Save for
this one instance a three-seemented condition of the
antennae appears to be universal in the South Indian form.
It is remarkable that this seven-segmented condition
should be found to persist in bugs collected in 1916 in
* T do not know where the author obtains his authority for this
statement. I can find no such remark in my description of the
species (“‘Cocc. Ceylon,” iii, p. 200). On the contrary, I have
distinctly stated (/oc. cit.) that “a constant succession of larvae is
produced during the life of the insect.”—E. E. G,
134 Mr. K. Kunhi Kannan on
Bangalore, when as early as 1913 the degeneration had
already taken place all over Mysore and Coorg. In Ban-
galore itself, specimens from the same locality and elsewhere
show the degeneration.
The variability in the number of segments in the an-
tennae appears to be of frequent occurrence in the genus
Lecanium, and also in Pulvinaria. I tabulate below the
variations noted by Mr. Newstead in his book on “ The
Coccidae of the British Isles,” and by Green in his “ Coc-
cidae of Ceylon,” the only literature on the subject to
which I have been able to gain access.
99
From “THe CocctpaAE OF THE BritrisH ISLES.
Normal No. Abnormal No.
of Segments. of Segments. Remarks.
Pulvinaria vitis . 8 6
3 floccifera 8 6
Lecanium persicae 7 6
rs ciliatum 8 7
4, bituberculatum 8 7
eS capreae 7 6or8
if nigrum ii 8
From “ THE CoccrpAE OF CRrYLON.”
ne ee ee
Pulvinaria tomentosa . tS 7
Lecanium capparidis . - uO 7 :
3 jormicarii . aS a
- acuminatum 5 83 7
es viride ; eT 8 through incomplete
division of the 4th.
= discrepans 7 8 from an_ obscure
division of the 7th.
is marsupiale . Y 8
- bicruciatum 6 7
ie longulum — . a fs} 9 probable.
es psidit u ;
An analysis of these variations shows that of the total
number of 51 species (42 Lecanium and 9 Pulvinaria)
described in the two books there is variation recorded in
17, viz. 334 per cent. of the number. Of these 17, the
variation is by the addition of a segment in 12, by the
reduction of a segment or two in 4 and by both m 1. It
is thus clear that the reduction from seven to three in
Coccus viridis cannot be placed in this category, but has
An Instance of Mutation, 135
to be classed separately, not only because the reduction
is by as many as four segments, but also because it is
inherited. There are only two cases on record which may
be held to approach this one, which I have not included
in the analysis above. These are Coccus acutissimus and
Paralecanium (Lecanwun) expansum. In the former Green
could only distinguish two basal segments, but he noticed
“lighter transverse marks which suggest an original
division into six or seven segments.” The antennae of
Paralecanium (Lecanium) expansum are described as
“with incomplete divisions, though a terminal one and a
basal two can easily be distinguished.” Whether the
nymphs of these two species were examined by Green is
not definitely stated. But the fact that there were traces
of six or seven segments in one and a terminal fourth in
the other makes it probable that, at any rate at the time
the species were described, the nymphs had six-segmented
antennae. And it is improbable that Green would have
omitted to examine the nymphs of the only two species
in which there is a reduction of antennal segments beyond
what he himself gives as the normal number for all nymphs
of the family Lecaniinae.
The reduction from seven to three segments in the
Mysore form must therefore be held to be unique. The
fact that it is inherited by the nymphs renders no longer
tenable the character of a six-segmented antenna in the
nymphs as a feature of the genus Lecaniwm. The Mysore
form is therefore entitled to specifie rank, and I propose
to name it Coccus colemani in honour of Dr. Coleman, as a
mark of gratitude for the valuable scientific training I
have received at his hands.
Coccus colemani, sp.n. (Plate V, figs. 2, 3.)
Adult 9 characters as in Coccus viridis. But antennae three-
segmented, the first and second segments subequal, the third from
five to six times the length of the first and having a number of
apical and subapical hairs. The dorsal x-wise carina not found in
any stage. Dermal cells more round than oval, scattered over the
derm and from 30 to 80 pw apart.
Colour pale lemon-yellow to greenish-yellow. Shape oval, the
anterior end being narrower but is liable to variation in specimens
fixed on the sides of veins of leaves in which the anterior end is
more or less acuminate, and either the right or the left side may be
136 Mr. K. Kunhi Kannan on
shortened and straight. The insect is ovoviviparous, but a few
eggs may be found laid occasionally. Reproduction continues for
about a month and a half after reaching the adult stage. The
number of young produced may reach over 500.
The newly hatched larva is of a pale greenish-yellow, broadly
oval. The antennae three-segmented as in the adult. The relative
lengths of the segments as in the adult. Other characters as in
the nymphs of Coccus viridis. Male unknown.
Length of adult 2-4 mm.
It may perhaps appear necessary to create a separate
subgenus for the reception of this new species, but I cannot
decide the question until I have made a more detailed
study of the group and examined C. acvulissimus and
P. expansum.
The sudden formation of C. colemani made it appear
probable that Coceus viridis was unstable. Green himself
savs that a new variety of his species was created by
Mr. Newstead from specimens obtained from Lagos, but
“that sufficient material was not examined to establish
the fact.” The report of the Department of Agriculture,
Uganda, for the vear 1916 states that a new form of “ green
bug ” found along with the typical form but with eicht-
segmented antennae and described by Mr. Newstead
originally as a subspecies has been given specific rank
under the name Coccus africanum. There was therefore
considerable justification for the belief that Coccus viridis
was a mutating species. Requests for specimens were
therefore made to the Entomologists of the Agricultural
Departments of all countries where ereen bug occurs, but
so far they have been received only from Ceylon, Java,
Hawaii, Seychelles, and Honolulu. Samples sent from
Ueanda were unfortunately lost in transit. The material
obtained is of very great interest.
The specimens from Ceylon, Hawaii, Seychelles, and
Honolulu are all true to the description of Green. The
Javan specimens, on the other hand, exhibit an enormous
variation. Prof. Keuchenius of Java remarks in a letter
received from him that “the variability of Lecanium
(Coccus) viride is a difficult and troublesome question.
Green in his standard work does not mention at all anv
variability, and therefore in the beginning I thought that
I had to do with two different species, but afterwards I
An Instance of Mutation. 137
came to the conclusion that Lecaniwm (Coccus) viride varies
strongly. On the same locality and the same garden and
the same kind of Coffee (but different trees) one may
distinguish the following forms—
“1. A large form with a very flat body, which is of a
clear green colour.
‘2. A smaller form with a more elevated body, which is
less acuminate in front and of a darker dirty greenish
colour. Between these extremes there exist all kinds of
nuances.”
The following are the descriptions of the two forms
referred to in Prof. Keuchenius’s letter.
The Round Form. (Plate VI, fig. 1.)
The margin nearly circular. The marginal setae stout and frayed.
The skeleton is thick. The dermal cells large, irregularly oval
towards the margin, approximate, and smaller and more circular
towards the centre. Body elevated to give a more or less elevated
shape. Colour dull brown to dull yellow. The loop more or lcss
inconspicuous. Dorsum thrown into minute transverse folds.
Antennae very variable in number and relative length of segments,
the more usual number eight. Measurements :—
Eength/Breadth :, 3/2:2, 5/2°5,.3/2:25, 2°6/1-75, 2-5/1-75,. 25/175,
D2 aaa t20/ 2s 3/25.) 2. Os.) DoD) 29 O25. 20) 1265.8 °2E 3°25/2,
3°20/2, .3°25/2, 2°6/1°75, 2°25/2, 3/1°75; 3°25/1°75, 2:25/1°75, 3/1°75,
3/2, 2°25/2, 2:5/1°5, 3/1°75, 3/2, 2/1°75, 2°6/2, 2°5/1°75, 3/2, 3/2 mm.
The Flat Oval Form. (Plate VI, fig. 2.)
Oval, flat, anterior extremity subacuminate. The marginal setae
less strongly developed but of the same shape as the round form.
The loop more or less conspicuous. The chitinous skeleton thinner,
and the dermal cells round, fewer, scattered and not approximate.
Colour varies from greenish-yellow to greenish-blue. Dorsum not
thrown into folds. Antennae more usually eight-segmented, but
very variable in number and relative length of segments.
Measurements :—
Length/Breadth: 4/2, 4/1°75, 4/2, 4°6/2, 3-5/2, 3°55/2, 3°25/2, 4/2,
4/2, 4/2 20, Utes 4 5/2, 4/2, 3/1°75, 2°75/1-75, 3/2, 2:°75/1-75, 3/2,
2: 20/2; 370/23 °5/2°25, 2°75/1°75, 4/2, 3/2,
: 7
138 Mr. K. Kunhi Kannan on
The antennal variability in these two forms is very great
and is disclosed by the following analysis :—
Round Form (of 25 examined). | Long Form (of 33 examined).
Antennae 8 segmentedin15 | Antennae 8&8 segmented in 16
jth OST 4 30 So RST u 6
es 8&6 S ipa a 7&7 sf 8
a 7&7 % dhe 55 7&6 ; 2
a 6&6 if 32 + 5&5 a 1
FA 6&5 = JEP
99 5&5 29 1
From this it appears that among the round form, of the
25 examined 1 had abnormal antennae, or 40 per cent.
In the long form of 33, 17 had antennal abnormality, or
51-5 per cent. The range of variation as shown in the
charts (Pl. VII, figs. 1 and 2) is very great and far exceeds
the limits of ordinary variation. It is not alone that
segments show a reduction in number and relative length,
but in the same specimens the antennae may be different
in the number and relative length of segments, producing
an asymmetry. The variability in size, “colour, shape and
elevation appears to continue to the same extent in the
specimens sent by Prof. Keuchenius in 1916 as when he
studied the pest two years previously.
Between these two varieties described above, there are
several intermediate forms, presenting several stages and
gradation in details of structure, size, colour, elevation
and conspicuousness of the loop, but they are mainly
grouped round these two types. From a study of the
material the impression is forced on one that the Javan
forms are highly unstable. Two of these forms described
above are entitled to : specific rank. One of these, the oval
flat form, may prove identical with the new form described
by Mr. Newstead as Coccus africanum. The other has,
so far as I am aware, not been described. I refrain from
creating species for the reception of these two, until I
have an opportunity to examine Coccus africanum.
These facts of variation prove that Coccus viridis is a
mutating species. In Mysore the bug was all but caught
in the act, and in Java the saltatory” variations contandes
In Uganda a new form has been in existence since 1898,
when C. africanum was first described as a subspecies.
There are two views possible in regard to this interesting
An Instance of Mutation. 139
phenomenon : (1) that Coccus viridis produces different
forms under the stimulus of different conditions; (2) that
Coccus viridis itself is a mutant from another unstable
species. One or both these may be true. If Coccus
viridis and the forms regarded as its derivatives all main-
tain the distance from other species, which entitled it to
specific rank, then the inference is justified that the
mutating species is C. viridis. If, on the other hand,
C!. viridis or one of its so-called derivatives structurally
approaches or is very nearly identical with another species
of scale insect and this latter is an unstable species, then it
follows that the mutating species need not be necessarily
C. viridis alone, but the species with which C. viridis or
one of its derivatives is found to closely agree.
We have now to see which of these alternatives has
application in regard to the variations described above.
The flat form from Java, the South Indian form, the
Coccus africanum of Uganda, are more or less referable
to Coccus viridis. But the round form from Java is dif-
ferent in structural detail. The round contour is not a
great difference, for it has been found occasionally among
the South Indian forms. The eight-segmented antennae
are common to C. africanum and to the oval flat form
from Java itself. The antennae are just like those of
P. psidii, as will appear from the charts (PI. VI). The
irregularly oval approximate dermal cells and the strongly
developed marginal setae are peculiar to the round form,
which makes it structurally identical with P. psidi as it
occurs in Mysore. Specimens of these placed under the
microscope so approach each other in structure that it
would be difficult to tell the difference except from the
contour, which is round in one and oval in the other. It
is not known what shape P. psidii takes in Java, but the
shape is as already indicated of very little consequence.
The structural similarity of the round form with P.
psidvi assumes a new significance and importance when the
variability of Pulvinaria psidii is considered. Its varia-
bility is a feature of this bug which Green himself has
noticed’ both in regard to size and anal plates. After
noting a minor variation in the length of the fourth segment,
he proceeds : “Valves of the anal operculum variable in
form in the same community and is particularly marked
in some examples from my rtle, of which no two individuals
are identical in this particular... , Length of insect
140 Mr. K. Kunhi Kannan on
averaging from 3-3°50 mm., but exceptionally large
individuals have reached 5 mm., some examples from
myrtle, while showing all the structural characters of the
type, were exceptionally small, the adult insect only
measuring 2 mm. in length, with a correspondingly small
ovisac.”’
To these variations have now to be added those of the
antennae, which as shown in the drawings are reduced
from the normal eight to as low as five (PI. VI, fig. 4).
In the same specimen, as in the Javan form, one antenna
may vary in one direction the other in another. Here,
again, the reduction may be greater than that which has
ever been noticed in other species of Pulvinaria, for im
psidw it may be by as many as three segments, whereas
in other species of the genus it is never greater than by
one or two segments.
These variations reduce the gap between P. psidir and
C. viridis. The differences between the two species are
tabulated below.
P. psidii. | C. viridis.
Shape oval, not variable.
Colour varies from dark or dirty
green to greenish-yellow, very
variable. Dull.
Antennae 8-segmented.
Oviparous.
Secretes meal to lay eggs in.
Chitin thick, loop therefore
invisible.
Dermal cells large, irregularly
oval, approximate towards the
but
round towards the centre.
margin, more or less
| Shape variable, one side straight
the other curved, rarely oval.
Greenish to pale lemon-yellow.
Not very variable. Shiny.
Antennae 7-segmented.
Ovoviviparous.
Does not secrete meal.
Chitin thin, loop therefore
visible.
Dermal cells round. -
The distinction between the antennae is of little im-
portance in view of the variation in both the species.
Tt has
already been shown that antennal segments in Pulvinaria
psidii may be reduced to as low as five.
As regards mode
of reproduction, though no P. psidit has shown any de-
parture from ovipary it is not unusual to find beneath
green bugs a few developed eggs.
in the genus Lecanium are oviparous.
The majority of species
Therefore it appears
An Instance of Mutation. 141
to me that the ovovivipary of vzridis is an advanced stave
transitional from ovipary. With regard to the loop the
presence or absence of it is by itself an unimportant dis-
tinction as it is only the appearance of the Malpighian
tubes which will be visible or invisible according as the
chitin is thin and transparent or thick and opaque. The
variations in P. psidii are so great that those of C. viridis
come within their limits. A similar remark holds good in
regard to size. The difference in the shape of the dermal
cells is not great. There are specimens of C. viridis in
which the dermal cells distinetly approach the shape and
arrangement in P. psidii (Pl. V, fig. 1). The main dis-
tinction on which Green appears to rely is, that P. psidi
secretes meal and viridis does not. But this distinction
breaks down, for in L. hemisphaericum, as I have found,
and as Green himself has observed, there is a secretion of
meal along the margin. Green says in regard to it that
“at this time (of gestation) the inner marginal surface 1s
dusted with white mealy powder, and where a scale has
been detached from the plant, an oval white ring marks
the previous position.” As a matter of fact the secretion
of meal is in much greater quantity than indicated in this
description, in ue of L. hemisphaericum from
Mysore (Pl. VIII, fig. 1).
There is also the fact that one apparently healthy mealy
bug has been discovered by me to lay eggs beneath the body
without a preliminary secretion of meal. Diseased speci-
mens have also been occasionally observed to lay eggs
without secreting meal. Furthermore, in green bug there
appears to be a secretion of meal, though in the minutest
quantity. When specimens are lifted off from the leaf
they do not always drop to the ground but often hang
by a thread, which must therefore be secreted by the bug
itself,* and Green notices the presence of wax-secreting
glands round the reproductive opening. The resemblance
goes further. I have already remarked on the feature of
psidi of being tilted at an angle to the surface of the host
by the secretion of meal beneath. This habit has been
found in large numbers of green bug.t In other species
* T think that the author has misinterpreted this phenomenon.
When one of the insects is detached without unnecessary violence,
it will often remain hanging by its long rostral filaments, which are
inserted into the tissues of the plant.—E. E. G.
peraeech Ries 253 ; ee Geen
+ The *‘ tilting” of the body, in L, viride, is usually a symptom
142 Mr. K. Kunhi Kannan on
of Lecanium (Coccus) in Mysore this habit has not been
found or is slight and inconspicuous. In Coccus viridis it
is so great that the dorsum may be thrown into minute
folds (PI. VIII, fig. 3). It is difficult to explain this except
as an inherited tendency persisting after the necessity has
clisappeared.
If the difference between psidic and viridis appears,
then, of little importance, the difference between psidi
and the Javan round form is much less. The structural
characters of these two are, as | have already shown,
identical. The only serious difference is in the method
of reproduction. The Javan round form is thus inter-
mediate between psidii and viridis. The series of forms
commencing from psidiz on one side and extending to
viridis and colemani on the other, exhibit a gradual de-
generation not by fluctuating variation but by saltatory
variations, or what De Vries would call retrogressive
mutations. or, on the one side, we have a meal-secreting
habit, more numerous and larger cells in the derm, strong
marginal setae, a larger size, and eight-segmented antennae,
and at the other end a smaller size and three-segmented
antennae, absence of meal, less numerous and more rounded
cells in the derm and very feebly developed marginal setae.
The intermediate types approach one or other of these
extremes, and some of them are extremely unstable. The
conclusion appears therefore to be justified, that Coceus
viridis arose as a mutant from Pulvinaria psidu, and the
various forms from South India, Java and Uganda are
derivatives from the latter species either directly or through
C. viridis.
This hypothesis that two species which are placed in
different genera have mutational relations is the only one
that fits the facts given above. Short of actual demon-
stration, it is difficult of acceptance at first sight, and
demonstration is difficult under the widely different con-
ditions of distant countries in which the mutations have
occurred. It does not appear probable that the various
forms so produced can all be produced in one of these,
especially when the parthenogenetic condition of these
forms prevents their crossing. South India yields only
of disease, and commonly occurs in the incipient stages of infection
by the parasitic fungus Cephalosporium. 1 have never observed a
healthy insect in this position.—E. E. G.
An Instance of Mutation. 143
one form; so also Ceylon. In Uganda the two types are
probably fairly fixed. Java, where the types are not yet
fixed and where the closest approach to psidii is found,
seems to be the most promising field for the experimental
demonstration of a common origin of the various forms,
though it appears unlikely that Coccus colemani will be
produced there.
Until these experiments are conducted in Java or else-
where (some of these are being attempted in Mysore), I
must look for confirmation of my hypothesis in facts
which have already been recorded by Coccidologists.
With regard to the two genera Pulvinaria and ‘Lecanium,
Green writes as follows in his book on ‘‘ The Coccidae of
Ceylon,” p. 258: “In all purely structural characters
there is nothing to distinguish the members of this genus
(Pulvinaria) from those ‘of Lecanvum, so much so that
until the period of oviposition it would be impossible to
determine whether an individual should be placed in one
genus or the other,” and later, on p. 264, when dealing
with P. psidw, he says, that “in its earlier stages the
insect bears a superficial resemblance to Lecaniwm (C occus)
viride, from which it may be distinguished by the absence
of the dark intestinal loop.”
Ne is even more emphatic. He says in his book
“The Coccidae of the British Isles,” that “this genus
comes very near to Lecanium (Coccus), and is only separable
from it by the formation of a cottony ovisac below and
behind the posterior extremity of the body of the adult
female at the period of parturition. . . . All the stages of
the male, including the glassy puparium as well as those
of the female up to the time of parturition, axe inseparable
from those of Lecaniwm (Coccus), so that in the absence
of the ovisac it is quite impossible to fix this otherwise
conspicuous genus.” The secretion of meal is found in
another important genus, Protopulvinaria, mm which the
meal is smaller in quantity, but is secreted all round the
margin. This genus has indeed been placed by Mrs. Fernald
under Pulvinaria as a subgenus, and I have already referred
to the secretion of meal in a species belonging to Lecanium,
viz. L. hemisphaericum. The secretion of meal is not,
therefore, an exclusive feature of Pulvinaria, but is found
more or less in the allied genera and in Lecaniwm (Coccus)
itself.
To turn now to the genus Pulvinaria, the variations I
144. Mr. K. Kunhi Kannan on
have indicated are in individuals. In a mutating species,
especially when it is found all over the world, there must
be well-marked varieties, and this is what we find. Apart
from the “ phytophagous”’ varieties, which are very
numerous in Mysore, there are others of a more permanent
character. The form of Pulvinaria psidv in the Philip-
pines has been given subspecific rank by Cockerell under
the name philippina. He says in his monograph on
“Coccidae from the Philippine Islands” (Putman Me-
morial Fund, 1905), “the long tibia, long third antennal
joint, marginal hairs, long bristles on joints 2 and 5 of
antennae, etek all show aie insect to be very close to
Pulvinaria ficus (Hempel) and P. psidii (Maskell). The
six-jointed antennae are distinctive, but may not be con-
stant. It is evidently reasonable to treat this insect as
a subspecies of psidiz, and so far as I can make out P. ficus
should stand as P. psidiv ficus.” That is to say, there are
two well-marked subspecies in P. psidw. With regard to
a third species, P. cupanae, Green says that it is doubtfully
distinct from P. psidii.
A more striking evidence of the consanguinity of the
various types I have dealt with is the variability of the
anal plates in all of them. Green says in his introduction
to the family Lecaniinae that their form and. size afford
good specific characters. These characters do not vary
with the size of the individual, but are practically constant
for each of the several stages, and on p. 236, in describing
the variety “* quadratum ” ‘of Lecanium expansum, he says,
“the size and form of the anal scales of the adult female
are usually so constant in any one species of Lecanvwm that
such a marked difference as is found in the present instance
must be looked upon as varietal.” Green has recorded
the variability of the anal plates in P. psidii and given
drawings of the various shapes they assume. The quota-
tions above indicate that this variability is an indication
of great instability. Now in the types which I regard as
derivatives of P. psidii it is not alone that the anal plates
are of the same shape when normal, but the variations
when they occur are more or less in the same direction.
They are more fixed in the more stable forms as Coccus
viridis, less fixed in Coccus colemani, and least in the
forms from Java. The shape of the anal plates and their
variability in the same direction is quite consistent with
the hypothesis I have advanced of a common origin.
An Instance of Mutation. 145
The tendency to regressive mutation exhibited by
these insects is probably due to the continued absence of
a sexual generation, which, if one may judge from the
behaviour of species similarly circumstanced, tells on the
vigour and vitality of the species. Though C. hesperidum
is one of the commonest species occurring on numerous
plants from the United States to Japan, no male has been
recorded at any rate from India, Java or Ceylon; nor
have males been recorded for C. viridis, the study of which
dates as far back as 1882, except for two doubtful ones
from Java.
The Weismanian theory that the purpose of sexual
reproduction is to induce variability has received no
support from the study of variation in parthenogenetic
forms, the results of which show that variability in such
species is not less than that in sexually produced forms,
and that therefore variability is not a factor necessarily
introduced by the union of the sexes. But from the fact
that parthenogenesis does not induce variability it does not
follow that it is the cause of it. I suggest it as a possibility
because the types I have been dealing with show a pro-
gressive degeneration, and because it seems to me that
the continued absence of a male generation prevents the
swamping effects of intercrossing, ‘and therefore affords a
ereater chance for the survival of variations. Whether or
not the continued absence of a sexual generation is the real
explanation of the instability of P. psidii, it is the sort of
species where one would look for mutation. Much the
same remarks apply to C. viridis, which take so many
different forms in different countries. There is thus con-
siderable justification apart from the facts I have already
given for the conclusion that C. viridis, C. colemani, @:
africanum, and the Javan forms are directly or indirectly
derived from P. psidii.
This conclusion is of great importance and interest. It
indicates that the parallelism in structure between genera
with ovisacs and those without them have an evolution-
ary connection, the ovisac condition being antecedent in
time. Such genera could be found in families other than
Lecaniinae. In Dactylopinae, for mstance, there is a
structural similarity between one oviparous and another
viviparous species in Mysore. In Pulvinaria itself, there
are probably other species which stand to species in Le-
canium in the same relation as psidii does to viridis. In
TRANS. ENT. SOC. LOND. 1918.—PARTS I, Il. (DEC.) L
146 Mr. K. Kunhi Kannan on
Mysore there is at least one instance where such relation
appears to occur. This is under investigation. It is sig-
nificant in this connection that there are several species
in Pulvinaria in which there are well-marked varieties.
Newstead merges in Pulvinaria vitis the following species,
P. betulae, P. salicis, P. oxyacanthae, and P. persicae, but
retains P. ribesiae as a variety. Similarly the limits of
variation are great in P. flocezfera, in which also a number
of species have been merged. The study of species like
these will throw considerable light on the relationships of
the various genera and species of Coccidae.
Even more important and valuable will be the instances
of mutation which the study is likely to bring to light. I
give below two instances which furnish a very close parallel
to the phenomena which I have describéd, where therefore
mutation must have occurred. Jn a most interesting paper
on “Some comparisons of Coccus citricola and C.. hes-
peridum,” Mr. H. J. Quayle, of the University of California,
gives an account of the relationships between the two
species, which are almost similar to those between P. psidia
and C. viridis. I summarise below the differences between
the two species.
C. citricola. C. hesperidum.
Antennae with 8 segments in | Antennae with 7 segments.
the great majority.
Ground-colour grey or dirty | Ground-colour distinctly yellow-
white. A more even distribu- ish. Colour pigment coalesced
tion of dark colour pigment. in more or less definite areas.
Lustre dull.
Shape oval, not variable.
Male found occasionally.
C. citricola is the more variable of the species.
“Tn 78 specimens of citricola in which 139 antennae
were examined there were three
joints in one antenna and eight in the other. In
says
Lustre shiny.
Shape variable: one side straight,
the other curved.
Male unknown.
Quayle
scales each with seven
four
scales there were seven joints in both antennae, and in
four others there were seven joints in one antenna, while
the other was not examined.
67, had eight joints in both antennae.
hesperidum examined all had seven joints.”
The remaining number, or
In 73 specimens of
The paral-
An Instance tof Mutation. 147
lelism between C. citricola and C. hesperidum, on the one
hand, and P. psidii and C. viridis, and C. viridis and C.
coleman, on the other, will now be obvious. There is one
apparent difficulty. Citricola is a species described in
1914, but hesperidum was described many years earlier.
According to my hy pothesis citricola should be regarded
as the parent species and as having been earlier in time.
It has, however, to be remembered that the mere fact of
an earlier record is of itself insufficient to prove the later
origin of a species. What has probably happened is that
hesperidum formed out of citricola crowded out the parent
species, and this would fit in exactly with my hypothesis
and with the observations in Mysore and other countries
where Pulvinaria psidii is seldom a pest, while C. viridis
and C. coleman are notoriously injurious to crops.
The second instance is that which has come to the notice
of Green, and to which he refers in the course of an in-
teresting letter received from him on the subject of the
phenomenon in C. viridis, brought to his notice. He
wrote as follows: ‘Such degeneration, if clearly estab-
lished, is extremely interesting, and so far as I know has
not been recorded before. Curiously enough since reading
this paper I have met with an instance that appears to be
of a similar nature. In examining some old material
from Java, I have found an insect that agrees in every
character with Phenacoccus mangiferae, described from
Ceylon, except that its antennae have only seven instead
of nine joints. According to the present classification,
this difference would necessitate the relegation of the
Javan specimens to a distinct genus (Pseudococcus). But
I am convinced that they are really conspecific.”
What has undoubtedly occurred in C. viridis is therefore
by no means an isolated instance, and I believe the study
of scale insects in the light of the phenomenon recorded
and described above will bring to light more instances of
mutation. We are still too ignorant of the obscure pro-
cesses involved in. this important phenomenon to neglect
what seems to me to be a promising field for its investi-
gation,
In conclusion, I have to thank Dr. Coleman, the Director
of Agriculture in Mysore, for his sympathy and guidance,
and through him Prof. Keuchenius of Java, Mr. C. C.
Gowdey of Uganda, Mr. Lyne, Director of Avriculture in.
Ceylon, Mr. P. R. Dupont, Curator, Botanic Station,
148 Mr. K. Kunhi Kannan on An Instance of Mutation.
Seychelles, Mr. Ehrhorn, Entomologist, Honolulu, for kindly
furnishing samples of green bug from their countries. I
am also indebted to Mr. K. E. Green for the encouragement
he gave me.
EXPLANATION OF PiatEes V-VIII.
Puate V, fig. 1. Coccus viridis, one of the first specimens sent in
for identification on the outbreak of the pest in Mysore in 1912.
Fig. 2. Coccus colemani. Fig. 3. C. colemani. Fig. 4. Larva of
C. colemani, just hatched. Note that there are only three segments
in the antennae.
Puate VI, fig. 1. The round form from Java. Note the dermal
cells. Fig. 2. The long form from Java. Note dermal cells.
Fig. 3. P. psidii. Fig. 4. Pulvinaria psidii.
Puate VII, fig. 1. Antennae of the long form from Java.
Fig. 2. Antennae of the round form from Java. Fig. 3. Antennal
variation in P. psidii, round form from Java, C. viridis, C. colemani.
Fig. 4. Variation in the antennae of P. psidii and stages of reduction
from the antennae of C. viridis to the antennae of C. colemani.
Fig. 5. Antennal variation in the abnormal round form from Java,
and the abnormal long form from Java.
PuatTe VIII, fig. 1. L. hemisphaericum turned over to show the
waxy secretion along the margin of the body, and the mark left on
the leaf as a result of the filaments adhering. Fig. 2. The secretion
of meal in P. psidii. Fig. 3. C. viridis showing the hind end of the
body tilted up much as in P. psidii. Fig. 4. Variations in the anal
plates of P. psidii from Green, of P. psidii from Bangalore, C.
viridis from Ceylon, and C. viridis from Bangalore.
( 149 )
VUT. Some Remarks on Mr. Kunhi Kannan’s Paper, * An
Instance of Mutation.” By KE. Ernest GREEN, F.Z8.
{Read March 6th, 1918.]
THE author records some extremely interesting observations
on a marked degeneration (that has appeared within quite
recent years) in the antennae of two nearly related Coecidue—
Lecanium (Coccus) viride and Pulvinaria psidit.
In the vear 1882 a ereen scale-insect attracted attention
in Ceylon as a serious pest of the coffee plant, though it
was not until 1886 that it was recognised and described
as a new species—under the name of Lecanwwm viride.
The same species was found to be infesting the coffee
plantations of Southern India a few years after its first
appearance in Ceylon. It does not appear to have been
noticed in the Mysore district until 1912, at which time
the insect is said to have been quite typical in regard to
the structure of the antennae. Mr. Kannan reproduces
a photograph of “ one. of the first specimens sent in for
identification at the outbreak of the pest,” which exhibits
seven-jointed antennae. Yet, by the following year (1913),
the Mysore examples of the insect—though otherwise
typical of the species—were found to have “undergone a,
remarkable degeneration which took the form of a reduc-
tion of the number of antennal joints to 5, 4, and 3, instead
of the normal number of 7. This (as may be gathered
from the author’s figures) was effected by a suppression
of intermediate divisions until—in the final stage—there
- remained only the normal Ist and 2nd joints, with a long
compound segment consisting of the other 5 joints with
little or no trace of the former divisions. It is now said
to be difficult to find a single example with antennae
showing more than three visible segments. From a
consideration of these facts the author arrives at the
conclusion that a new species has been suddenly evolved,
and he proceeds to describe it—under a new name—as
Coccus colemani.
T have had no opportunity of examining examples of
this insect, but presuming that if has been correctly identi-
fied and that it is res ally a sudden mutation from the original
Lecanium viride, it still seems questionable if there is
TRANS. ENT. SOC. LOND. 1918,—PARTS J, Ul, (DEC.)
150 Mr. E. Ernest Green’s Remarks on
sufficient justification for the erection of a new species. I
should prefer to regard it as merely a local race or—at
most—allow it to rank as a subspecies. But Mr. Kannan
goes so far as to suggest the propriety of erecting a new
subgenus for its reception
Students of the Coccidae are beginning to realise that
too much reliance has been placed upon antennal characters
as a factor in classification. There is scarcely a single
species that does not exhibit variability in one direction
or another—in colour, size, or form, or in the structure of
one or more of its organs; and it is in the antennae that
variation is most liable to occur.
Mr. Kannan describes also what he considers to be two
abnormal forms from Java, which he believes to have been
similarly evolved from L. viride. From his deseription,
one of these (the round, convex form) would appear to be
2 new species, while the other is probably identical with
L. africanum—a species which the author believes to have
been equally derived from wiride. It would be interesting
to know whether these Javan insects have been submitted
to any expert opinion.
But the most important part of Mr. Kannan’s paper is
concerned with his hypothesis that Lecanium viride itself
is a direct mutant from Pulvinaria psidiz. From the title
and sub-title of his paper, it may be judged that the author
considers that he has fully proved his case. I must confess
that his arguments—though most ingenious—-are scarcely
convincing, and appear (to me) to be founded upon in-
sufficient evidence.
The main argument, when analysed, appears to be as
follows :—
1. Lecanium viride has suddenly evolved a distinct:
variety with 3-jointed antennae.
2. There are allied species, subspecies, or races in Africa
and Java.
3. L. viride “is therefore clearly unstable.”
Pulvinaria psidii is subject to variation and has
eee forms in otber countries.
L. viride and P. psidit resemble each other super-
ficially and occupy the same regions.
6. Therefore L. viride is a mutant of P. psidii. Q.E.D.
This, of course, is a very bald way of stating the case.
Our author marshals a large array of evidence—or supposed
“An Instance of Mutation.’ Li
evidence—in support of his theory; but much of this is
open to question, The first four clauses may be accepted
x 220
A comparison of various organs of Lecanium viride and Pulv.
psidvi. (The figures have been drawn to scale, with the aid of a
camera lucida; each pair being amplified to the extent that best
shows their relative proportions. )
Lecanium viride. Pulvinaria psidii.
1, antenna, X 220. 2, antenna, x 220,
B, mid leg, x 80. 4, mid leg, x 80.
5, posterior spiracle, < 280, | _6, posterior spiracle, x 280.
7, marginal hair, < 450. 8, marginal hair, x 450.
9, anal operculum, 135. _ 10, anal operculum, 135.
almost without comment, except that I may point out
that the third does not necessarily follow upon the second,
152. Mr. E. Ernest Green’s Remarks on
With regard to clause five, I hold the opinion that the
resemblance is superficial only. In his tabulated differ-
ences between viride and psidii the author pays no atten-
tion to dimensions, and there is nothing to indicate whether
his figures are drawn to scale or not. Though the over-all
measurements of the two insects fall within the same
range of variation, this is by no means the case with respect
to the size of the various organs and the proportionate
lengths of the joints of the limbs. In spite of the fact
that the two insects are of approximately the same size,
it will be seen (vide accompanying text figures) that all
the organs of viride are very much smaller than the corre-
sponding structures of psidii. Taking these in order, we
find that the length of the antenna of typical viride is to
that of psidii in the proportion of 55 to 97, A still more
striking contrast is seen in a comparison of the legs of the
two species, which are in the proportion of 6 to 15 (femur
11 to 28, tibia 7 to 22, tarsus 5 to 11). The proportions
of other organs show corresponding differences : anal
operculum (length) as 8 to 11, (breadth) as 18 to 25;
orifice of posterior spiracle, as 9 to 17; marginal hairs, as
2 to 13. The relative proportions of the joints of indi-
vidual limbs also show strong points of ‘difference : in
viride, the femur is to the tibio-tarsal member as 11 to 12
and the tibia is to the tarsus as 7 to 5; while, in psidi,
the same members are in the proportion of 28 to 33 and
22 to 11 respectively. Thus we find that, while in viride
the tarsus and tibia are approximately equal in length,
in psidw the tibia is twice as long as the tarsus. The
relative lengths of these two joints are usually accepted as
useful specific characters.
The fact that a reduction in the number of antennal
joints has been observed in South Indian specimens of
both viride and psidi does not, in my opinion, provide an
argument in favour of the transmutation of the two species ;
but suggests, rather, that a similar environment has
induced a tendency to variation in the same direction.
The author remarks that “the main distinction on
which Green appears to rely is that psidii secretes meal
and viride does not.” I am sorry if any such opinion is
to be gathered from my descriptions of the two species.
I maintain that the similarity is purely superficial, and that
an examination of the microscopic characters would make
it impossible to confuse the two insects.
Trans, Ent. Soc. Lond., 1918, Plate V.
André, Sleigh & Anglo, Ltd.
MUTATION IN COCCIDAE.
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i : <
” m vd i
ve ° fi ‘ rere i -
= 2 : yr
1 7 ®
Pant *
+
Trans. Ent. Soc. Lond., 1918, Plate VI,
André, Sleigh & Anglo, Lid.
MUTATION IN COCCIDAE.
Trans. Ent. Soc. Lond., 1918, Plate VII.
a pestdi fram Bangalor
3 / . ay)
C_ liridss fron — Ceuton
\
CC) Viridts fron Bangalore
Howmd form from Awa
L / L
> 5
Long form from Java
|
Biche cl baad ss
C. Colemain 4
André, Sleigh & Anglo, Lid.
MUTATION IN COCCIDAE.
Trans. Ent, Soc. Lond., 1918, Plate VIII,
André, Sleigh & Anglo, Lid.
MUTATION IN COCCIDAE,
ae ae ne ihe
io
nibs as ot ek a a Sand =
i Gy trays Sait Ne ES eh OE idee ites
nent ae han”
ra e ye 7
ve
‘yi a ; Warn sa, yee
i & dl Ota Ry a ed
; wa Ae fi ‘4 Aw
Aen a ay
ate _ iq eS)
foal a
.- 6F
‘An Instance of Mutation, 153
Much stress is laid upon the presence of a slight deposit
of mealy powder beneath the bodies of certain species of
Lecanium; but the secretion of wax—in greater or less
profusion—may be said to be common to the whole family
of Coccidae. In some it is profuse, in others it is small in
quantity and restricted to definite areas of the body. It
is not the secretion of meal that distinguishes the genus
Pulvinaria, but the construction of a definite ovisac. I
may remark, however, that I do not attach any great
value to generic distinctions, but regard them oreatly. as a
matter of convenience
I am quoted as writing (in the “* Coccidae of Ceylon ’’)
that “in all purely structural ieee ae there is nothing
to distinguish the members of this genus (Pulvinaria) from
those of Lecanzum; so much so that until the period of
oviposition it would be impossible to determine whether
an individual should be placed in one genus or the other.”
This statement is applicable only to the genera, and must
not be held to imply that two known species could not be
distinguished at an earlier stage.
In conclusion, I see no more justification for regarding
Lecanium viride and its alhes as having been directly
derived from Pulvinaria psidu than for assuming a similar
relationship between L. hesperidum and P. floccifera, ox
many other pairs that might be mentioned. By a skilful
manipulation of figures and charts it might be made to
appear that all the genera and species of the Lecuniinae
(or of any of the other subfamilies) were in an active state
of flux. There is no doubt that the genera Pulvinaria
and Lecanium are very closely allied, but their boundaries
are quite well defined.
After the kind acknowledgment of encouragement, in
the final paragraph of Mr. Kannan’s paper, I feel that the
above remarks have placed me in a rather invidious
position, and may seem to savour more of discourage-
ment than the reverse. But I really consider that the
author is to be congratulated upon having brought
together so many interesting and valuable obecrtions:
and having drawn attention to the close inter-relationship
that undoubtedly exists between many species and genera
of Coccidae. Though I have been unable to agree w ith all
his conclusions, I feel that a broader view of the subject—
such as he has here attempted—will be greatly to our
advantage, and I trust that Mr, Kannan will continue
154 Mr. KE. Green’s Remarks on * An Instance of Mutation.’
and extend his studies. Published work on Coccidae has,
hitherto (apart from the economic side), been too much
confined to pure systematics—to the making and remaking
of new species, or to the upsetting of well-established
names. Further research, in the direction in which
Mr. Kannan has led the way, will assuredly produce
valuable results, and may even revolutionise our present
knowledge.
IX. Observations on the Lepidopterous Family Cossidae
and on the Classification of the Lepidoptera. By
A. JEFFERIS TURNER, M.D., F.E.S.
[Read March 20th, 1918. ]
Ir has long been known that moths belonging to the
family Cossidae present certain peculiarities in their
neuration; but the importance of these peculiarities and
the light they throw on the relationship of the different
famihes of the Lepidoptera have never, I believe, been
fully recognised. So far as I know, no monograph has
appeared on the structure of the whole family. Mr.
Meyrick in his “ British Lepidoptera’? deals with three
genera, which he divides into two families rather widely
separated in his scheme of classification. Sir George
Hampson has dealt with the more numerous Indian genera
as one family in his “ Moths of India,” and has also kindly
lent me an MS. key to the world genera represented in the
collection of the British Museum. Mr. Barnes and Mr.
McDonough have revised and tabulated the North American
genera (Contrib. Nat. Hist. Lep. N. Amer.,” i, p. 3).
Without attempting a systematic revision of the world
genera, I have endeavoured to describe all the more
important structural modifications exhibited by them, and
to discuss their significance. The accompanying figures
are all original, and though roughly diagrammatic, for i
have no skill as a draughtsman, they give, I believe, with
accuracy the essential details of the neuration in each case.
Family COSSIDAE.
Definition.—Tongue and maxillary palpi obsolete. Fore-
wings with an areole, usually large; the parting vein
between areole and cell (the chorda) “distinctly or strongly
developed ; * a branched median vein distinctly developed
in cell, very rarely unbranched; two anal veins Ic and 16,
the latter furcate at base. Hind-wings with a branched
median vein in cell distinctly developed, very rarely un-
branched; three anal veins Ic, 1b, and la, 1b often shortly
furcate at base.
* With one exception, which will be described.
TRANS. ENT. SOC. LOND. 1918,—PARTS I, II. (DEC.)
156 Dr. A. Jefferis Turner’s Observations on
By this definition the genus Paracossus, Hmps., is
excluded from the family, and will be dealt with separately.
To the definition the following particulars must be
added : Moths of moderate or large, sometimes exceedingly
large, size. The larvae so far as "known, and probably in
every case, are internal feeders living in wood. The frons
is usually flat, but may have a projecting tuft of scales.
The labial palpi may be moderate and porrect, or short,
or obsolete. The antennae are rarely simple in both sexes,
frequently bipectinate in both sexes to apex, in one genus
unipectinate, frequently with a double row of long pecti-
nations in the ¢ for part of their length, the pectinations
Recrit is
cite
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Fic. 1.—Cossodes lyoneti, Fie. 2.—Dudgeona actinias,
White. Turn.
usually ceasing or shortening abruptly, and the apices
simple or shortly bipectinate, “but simple or shortly bipec-
tinate from base to apex in the 9. The tibial spurs are
long and well developed in some of the more primitive
genera, but frequently very short or obsolete. The frenulum
is sometimes short, not articulating with the retinaculum,
and apparently non-functional.
We will commence our survey of the neuration with two
of the most primitive genera, Cossodes and Dudgeona.
Both genera have long, ‘well- developed tibial spines and
rather long palpi, which are unusual in the family, and
confirm the conclusion, that I draw from their neuration,
that they are primitive types. Cossodes has simple antennae
the Lepidopterous Family Cossidae. 157
in both sexes, and contains one Australian species. The
type of Dudgeona is Indian, and has the 3 antennae shortly
bipectinate to apex, and veins 6 and 7 of the hind-wings
are separate; D. actinias, Turn., from Australia has the
antennae simple in both sexes, and 6 and 7 of the hind-
wings connate; there is a third unnamed species from
Africa, which is intermediate, having the g antennae
simple, but 6 and 7 of the hind-wings separate. In view
of their close specific relationship and agreement in all
other structural details, 1t does not seem necessary to
divide the genus. In neuration Cossodes and Dudgeona
are closely allied. Both possess an areole of moderate size
in the fore-wing, with a branched median nerve in both
wings. The areole be-
tween 8 and 9 is com-
pleted not by the usual
anastomosis, but by a
short cross-bar, probably
a mote primitive arrange-
ment. It is interesting to
note that in one example
of D. actinias examined
this cross-bar was absent,
leaving the areole open.
The fullimportance of this
observation will be seen
later. The Australian
genus Ptilomacra has,
like many others of the Fic. 3.—Ptilomacra senex, W1k.
family, lost its tibial
spurs, the antennae of both sexes show a double row
of long pectinations to the apex, in the 3 very long, the
palpi are small and very hairy, but in its neuration it
agrees very closely with the preceding genera, the only
differences in the fore-wing being a-larger areole, and
stalking of veins 7 and 8. The European Cossus is not
very far removed from Pétilomacra in neuration (fig. 21),
the principal difference being the smaller and more pro-
jecting areole, on the apex of which the origins on F389
10 are crowded together, and the obsolescence of the dorsal
half of the basal fork of 1b, which is vestigial. It has the
antennae shortly and evenly bipectinate to apex in both
sexes, the palpi moderately short, the tibiae without spurs,
and the frenulum in the 3, though stout, apparently
158 Dr. A. Jefferis Turner’s Observations on
functionless, being short and not articulating with a
retinaculum. Muacora agrees in neuration with Cossus,
but has occasionally, not always, an oblique bar from
near the end of cell to vein 8 imperfectly developed; it
is doubtfully. distinct. Hremocossus, Hmps., has very
Fic. 4.—Eremocossus foedus, Swinh.
similar neuration. I take the opportunity of figuring an
abnormal hind-wing of Eremocossus foedus 2 in which two
of the missing radial veins appear to be developed, one
(a) running from the cell into 8, the other (6) running
from the stalk of 6 and 7, quite distinct but ending in
Fig. 5.—Xystus robiniae, Bdv. Fia. 6.—Holocerus nobilis, Stgr.
dise without reaching margin. On the other side of the
same example and in both wings of a ¢ these extra veins
are wanting. In the Nearctic genus Xystus, which is a
member of this group possessing well-formed but rather
small tibial spurs and moderate palpi, this vein (a) 1s
constantly developed in the hind-wing. Except for this
the Lepidopterous Family Cossidae. 159
the genus presents only minor peculiarities of neuration.
The “‘Palaearctic Holocerus, to which the African Rethona
is Closely allied, is another member of this group with
moderately developed tibial spurs.
Fic. 7.—Dyspessa ulula, Fira.
Bork.
In the hind-wing the
234
8.—Stygia australis, Latr.
lower branch of the median is often so close to the lower
discocellular as to be nearly fused with it. In Dyspessa
this has actually occurred, so
that the median of this wing
appears single, only the upper
branch being left. In a third
Palaearctic genus of this series,
Stygia, the median is unbranched
in the fore-wing also, a rare de-
gradation of the neuration in this
family, though common in other
groups. In one specimen the
median in the fore-wing is Just
branched, forming a minute
median cell, and I have repro-
duced this also in the figure; it
is interesting as showing that the
median cell has been obliterated in
normal specimens by coalescence
' 0 G
Oulama australis,
WIk.
Kia. 9
of the two primary branches of the median.
Stygia marks the extreme development along one branch
of the Cossidae, and we must now hark back to a more
primitive Australian genus, Culama, which differs from the
ancestral form in only one point of importance, the origin
of vein 11 from the areole, which is large. Veins 8 and 9
160 Dr. A. Jefferis Turner’s Observations on
are stalked, but in Culama expressa, Luce. (fig. 22), which
should form the type of a new genus,* all the veins arise
separately from the areole. Both forms have the tibial
spurs well developed, as have the allied Neotropical genera
Schausiana, Strand (Hemipecten, Dyar), and an aidesenived
genus (sp. norax, Druce), which differ from them in minor
points only. The former has the antennae unipectinate in
both sexes.
The section of the Cossidae with hypertrophied areole
giving origin to vein 11 form a large proportion of the
family, anal so far as I know, no anak structure occurs
elsewhere in the Lepidoptera.t It may be explained in two
ways: (1) the origin of the chorda has been displaced
towards the base of the wing—that this has occurred is
shown by the increased length of the areole; (2) the basal
part of vein 11 may have
partly coalesced with the
common stalk of the re-
maining radial veins (the
radial sector) and with the
common stalk of the Ist
and 2nd radial. The latter
; factor has been also in
Fra. 10.—Phragmatoccia parvipuncta, Operation, and it explains
Hmps. the displacement of the
origin of 11 towards the
apex. The relative part taken by ‘the two factors could be
approximately determined by comparative measurements.
There are in the genus Phragmatoecia two types of
* Macrocytlara, gen. nov. Frons with anteriorly projecting
scales. Palpi moderately long, projecting beyond frons, longer
in 2, smooth-scaled; terminal joint stout, obtuse, in 3 very short,
in 2 rather long. Antennae bipectinated to apex in both sexes;
or in § only, in 2 simple. Thorax with a small posterior crest.
Tibiae with all spurs present and well developed. Fore-wing with
areole very large, median vein branching about middle, lower
branch ending between 4 and 5, upper between 5 and 6; 2 from
towards end of cell, 3 from angle, 4 and 5 separate, 6 from near
upper angle, 7, 8, 9, 10, and I1 arising separately from areole.
Hind-wings with medi vn cell narrow, lower branch ending between
4 and 5, upper peavcen 5 and 6, where discoc ee are sharply
angled inwards; 2 from about 2, 3 from angle, 4 and 5 widely
separate, 6 and 7 stalked from upper angle, 8 free.
t+ Except, as pointed out to me by Mr. Durrant, the Tortricid
Phtheochroa. In the Drepanidae, 11 sometimes arises from the
areole, but in this instance 1] arises from much nearer the apex.
the Lepidopterous Family Cossidae. 161
neuration in the fore-wing so different that at first sight
one would pronounce them distinctive of two separate
genera. In P. parvipuncta, Hmps., the structure of the
fore-wing is substantially the same as in Culama, but in
P. castaneae, Hb., the sector runs into the upper branch
of the median and the shape of the areole is distorted.
Although these two types of neuration seem so distinct,
some other species, such as P. impura, Hmps., present
intermediate forms, in which the anastomosis between
chorda and upper median is incomplete. The hind-wing
in this genus is similar to that of Culama, but is more
4
q
Fig. 11.—Phragmatoccia Fira. 12.—Xyleutes crassa, Drury
castancac, Hb. (polioplagu, Hmps.°.
primitive. In all the preceding figures the me branch
of the median, which is the common stalk of veins 5 and 6,
terminates between those veins; but the median cell has
been narrowed so that the lower branch, which is the
common stalk of veins 3 and 4, terminates either opposite
4 or between 4 and 5. Also veins 6 and 7 are separate
and parallel. For these reasons I am unable to regard
Phragmatoecia as a direct derivative of Culama; but un-
doubtedly Phragmatoecia is derived from the stem from
which Culama arose. The former genus is in other respects
less primitive than the latter; it has the antennae shortly
pectinated nearly to the apex in both Sexes, but in the 3
the pectinations are long for the basal 3 and then become
TRANS. ENT. SOC. LOND. 1918.—PARTS I, II. (DEC.) M
162 Dr. A. Jefferis Turner’s Observations on
abruptly shorter, the palpi are short and hairy, and the
posterior tibiae have a minute pair of terminal spurs only.
By far the largest genus in the family, Xyleutes, Hb.,
type crassa, Drury ( Chaleidica, Hb., Endowyla, H. pce
Duomitus, Butl., Himaeya, Moore, Az ygophleps, Hmps.), 1
represented i in all the warmer regions, but most cies ele
in Australia. The neuration is that of the more primitive
form of Phragmatoecia, and it differs from that genus only
in the scaling of the head and palpi, but the fore- wing is
very constant in structure, only slight differences existing,
such as the short-stalking of vein 9, or the lower branch
of the median terminating opposite 4 instead of opposite 5
as in crassa, or even from shortly before 4, but the median
Fig. 13.—Xylotrypa strigillata, Feld.
cell of the fore-wing is always narrow, not broad as in
Leuzera.
An undescribed genus,* which contains the species
strigillata, Feld., from temperate South America, is an
interesting modification of X? yleutes. The fore-wing and
antennae are the same, but the palpi and tibial spurs are
obsolete, and in the hind- -wing of the 3 there is a branch
running from vein 7 to 8. This, I think, represents one
of the veins of ae wing usually undeveloped. It is
variable, and in a Q ex ample represented by only a short
spur on the dorsal side of 8. As there is only one example
of each sex in the British Museum I cannot say whether
the variation is sexual.
* Xylotrypa, gen. nov.
the Lepidopterous Family Cossidae. 163
The genus Zewzera presents a curious mixture of charac-
ters, some specialised, others primitive. Of the former are
the absence of palpi and tibial spurs, and the 3 anicnnae,
which have a double row of long pectinations tO about 3
and then become abruptly simple. Of the latter is as
termination of the lower branch of the median between
veins 3 and 4 not only in the hind-wings, as in the pre-
ceding two genera, but in the fore-wings also. There is
also a bar between vein 8 and the cell in the hind-wings,
which may merely represent an anastomosis, but probably,
as in Xylotrypa, represents the vein marked in fig. 4.
There is some variability in the genus. In Z. coffeae the
areole is larger than in Z. aesculi, and vein 11 arises from
Fic. 14.—Zeuzera aesculi, Latr. Fic. 15.—Zeuzera coffeae, Neitn.
only just behind it. In aesculi 7 of the hind-wings arises
from the connecting bar, in coffeae from the cell. Z. indica
has the fore-wing as in aesculi, the hind-wing as in coffeae.
In Z. multistrigata 9 arises from the areole, connate but
not stalked with 8. In an unnamed species from South
Africa the chorda runs into the upper branch of the
median as in some species of Phragmatoecia. The fore-
wing of Zeuzera being as regards the unnarrowed median
cell more primitive than in any other genus, it must have
arisen independently from the same stem from which arose
Xyleutes and its allies, but at a lower level.
We complete our survey of the family with a group of
Neotropical genera, some species of which have invaded
North America, in which there is a tendency to reduction of
164 Dr. A. Jefferis Turner’s Observations on
the areole and median cell, the latter being sometimes lost.
Apart from the neuration they are characterised by small
palpi and tibial spurs; the latter appear to be sometimes
Fia. 16.—Givira tristis, W1k. Fie. 17.—Ingurimor pha
basalis, Wk.
absent, and by the g antennae being shortly bipectinate
from base to apex. Sometimes the frenulum is short and
apparently functionless. Gira resembles Zeuzera, and like
it has a bar connecting 8 with
u the upper angle of the cell in the
hind-wings, but both areole and
median cells are narrower. A
peculiar character not previously
noted in this paper is a connect-
ing bar between 1b and 1c of the
hind-wings towards their distal
extremities. This is, I believe,
only paralleled elsewhere in the
Psychidae, but I do not think it
indicates any close relationship
with this family. It has been
probably an independent develop-
ment. ILngurimorpha is a further
Via. 18.—Stenocyltlara
sabulosa, Schaus. development of the same stem,
with median cell obsolete in both
wings. An undescribed genus containing sabulosa,* Schaus,
is near Guvira, but lacks the bar in the hind-wings. Its
median cells are narrow, that of the hind-wings being very
* Stenocyllara, gen. nov.
the Lepidopterous Family Cossidae. 165
small. The connection between 16 and le of fore-wings
is not developed, the latter vein becoming obsolete before
it reaches the point of connection in Givira.
Lentagena is remarkable for its minute areole, which if
not carefully looked for might
be thought to have been com-
pletely lost.* It well illustrates
the process by which the areole
becomes obliterated by coal-
escence of its upper and lower
enclosing vein-trunks. In the
fore-wings there is an oval
median cell of some size, but
in the hind-wing there is none,
and the unbranched median
vein has been displaced towards ane A Teianenn wiskoné.
the dorsal margin of the cell. Schaus.
At first sight it Jooks as though
the upper branch of the median had become obsolete, but
comparing it with Lng: wrimor pha, in which the termination
of the median above vein 5 shows that the upper branch
is represented, it seems to me at
least equally probable that the
median has become displaced
dorsally after coalescence of its
branches. In this genus the 3
antennae are dentate or shortly
bipectinate to apex, the palpi are
rather small, and there appear to
be no tibial spurs.
I have not seen any example
of Trigena, Dyar, in which there
is stated to be no areole, but
there is certainly none in the
species tigrata, Schaus, which I am
unable to refer to any described
genus.t In this the neuration of the hind-wing is that
of Lentagena, excepting for the presence of a connecting
* Mr. Dyar, Proc. U.S. Nat. Mus., xxix, p. 178 (1906), describes
Lentagena as having no areole. This may, for all I know, be the
case sometimes, but I have examined one example cach (all that
are accessible to me) of tristan?, albicosta, and nudaridia, and found
it present in all of them, though in the last, which is the type species,
certainly very minute.
+ I propose for it the name Acyttara, gen. nov.
Fic. 20.—Acyttara igrata,
Schaus.
166 Dr. A. Jefferis Turner’s Observations on
bar between 8 and the end of the cell. In the fore-
wing there is a small median cell, but no trace of an
prcale: 6, 7, 8, 9 are stalked, and the anal veins anastomose,
16 running into le. The tibial spurs are obsolete; the
palpi moderate, porrect; the frenulum well developed, and
the 5 antennae bipectinate to apex.
This concludes my p’esent study of the neuration of the
Cossidae. I have not attempted to figure every genus,
but, so far as I know, I have not omitted any important
deviation of structure. As a result I have convinced myself
that this is a natural and compact family not divisible
naturally even into subfamihes. There is, it is true, a
considerable and very interesting degree of variation in
several directions, but all these lines of development are
linked together by forms of intermediate structure.
I have also convinced myself that the Cossidae have
retained the most ancient form of neuration among the
existing families of the Lepidoptera Heteroneura, and that
from this neuration that of all the other families can be
easily derived by a process of reduction, the stages of
which can be readily traced. The study of this family
has therefore appeared to be of fundamental importance,
and it is this that has encouraged me to consider it in
detail. But to establish my savalloesan it 1s necessary to
study also the neuration of these other groups, more
particularly of those families that may be considered of
primitive type, or at least to contain genera of primitive
type. Naturally this survey cannot be undertaken in an
exhaustive manner within the limits of a short paper.
I can do no more than select one or two of the more
primitive genera in the case of each family, paying par-
ticular attention to those families which agree with the
Cossidae in the primitive character of possessing three anal
veins, la, 1b, and 1c, in the hind-wing. These families are
the Tortricidae, Tineidae, Castniadae, Zygaenidae, Lima-
codidae, Psychidae, and Pyralidae.
THE CLASSIFICATION OF THE LEPIDOPTERA.
Before considering the relationship of the Cossidae to
other families it is necessary to make a few remarks on
the classification of the Lepidoptera. It is now generally
agreed that the primary division of this order is into two
very unequal groups, (a) those with closely similar fore-
the Leyidopterous Family Cossidae. 167
_and hind-wing neuration, and (6) those with unlike neura-
tion of the two wings, the number of the veins in the
hind-wings being considerably reduced. For these two
groups I ‘accept the names proposed by Mr. R. J. Tillyard
in a short but illuminating paper (Proc. Linn. Soc. N.S.W.,
DIT ps VOT) e Of Lepidoptera Homoneura and Lepidoptera
Heteroneura. These names are preferable to Jugatae and
Frenatae, for the number of the veins is of more importance
than the presence or absence of the frenulum, and as the
latter organ is present in two other orders of insects besides
the Lepidoptera, namely, the Mecoptera and the Newroptera
Planipenma (Tillyard, l.c., p. 174), it is probably more
primitive than has been supposed, and its absence in the
Lepidoptera Homoneura may well have been due to loss.*
The Lepidoptera Homoneura consist of the Micropterygidae
and Eriocranidae (if these are really lepidopterous) and the
A B c
Ce re
re
Hemalidae. I regard them as offshoots of the primitive
lepidopterous stem and not as part of the main line of
development, as illustrated in the accompanying diagram.
The dotted line represents the present era. Deeply
beneath it is the primitive lepidopterous stem, three
branches of which reach the surface; A represents the
Micropterygidae and Eriocranidae, B the Hepialidae, and
C the Lepidoptera Heteroneura. There is no evidence that
the two former were ever more numerously represented in
previous eras than at present, though that is quite possible,
but the third are a dominant group at the present day,
consisting of a vast number of genera and species, and are
consequently represented by a wide-based inverted cone.
The structure of the Lepidoptera Homoneura is of great
interest in the evolution of the order, but has small con-
nection with the object of the present essay, the natural
* Mr. Tillyard has since this was written sent me a drawing and
photographs demonstrating that a frenulum is actually present in
the Micropterygidae.
168 Dr. A. Jefferis Turner’s Observations on
classification of the Heteroneura, and I shall reserve the
former for future consideration.
It is also desirable to look at the neuration from a broad
standpoint and to bring it into correlation with that of
other related orders of insects. Without entering into
fuller discussion, I may say that I consider the primitive
lepidopterous wing possessed four main veins, which divided
dichotomously, together with three, or perhaps four, anal
veins. These veins (figs. 21 and 22) were the subcostal
(the costal exists as a separate vein only in fossil insects),
Fig. 21.—Cossus cossus, Linn.
S. Subcostal vein. R. Radius. M. Media. Cu. Cubitus. a. Areole.
m.c. Median cell. r.s. Radial sector. chk. Chorda. R1, 2, 3, 4, 5.
The five radial veins. M1, 2, 3, 4. The four median veins.
Cula and 1b. The two cubital veins. lA, 2A, 3A. The three
anal veins.
the radius, the media, the cubitus, the first anal, the second
anal, which is fureate at base and probably represents two
coalesced veins, and in the hind-wing the third anal. The
nomenclature adopted is that of the Comstock-Needham
system, and brings the lepidopterous neuration into corre-
lation with that of at least several of the primitive orders
-o
of insects (Tillyard, J. ¢., p. 173). In the accompanying
figures of Cossus and Macrocyttara the Comstock-Needham
notation is given, and in the former the commonly used
numerical notation also. The radius divides dichoto-
mously into the first radial and the common trunk of the
second, third, fourth, and fifth radials, which 1s known in
the Lepidoplerous Family Cossidae. 169
other orders as the radial sector. This again divides into
(a) the common stalk of the second and third radials, and
(b) the common stalk of the fourth and fifth. The latter
is of such importance in the Lepidoptera that it is necessary
to give it a special name, and I have termed it the chorda.
It is noteworthy that, although the original dichotomy is
often obscured, the second and third radials, that is, veins
10 and 9, always arise by a common stalk. The enclosed
space, completed by a bar or anastomosis between 9 and 8,
is identified by Mr. Tillyard with the discoidal cell, but as
that term has been used with a different sense in the
Lepidoptera, | have thought it wiser to retain for it the
=
ia. 22.— Macrocylttara expressa, Lue.
name areole. When areole and cell coalesce to form what
I will call an areocel, it is evident that the original stalking
of 9 and 10 is obscured, so’ that they appear to arise
separately from the areocel as in fig. 23. The media divides
into (a) the common stalk of the first and second median,
and (b) the common stalk of the third and fourth median;
between them is the median cell. Mr. Tillyard has shown
(l.c., p. 169) that the fourth median has coalesced with the
first cubital, thus closing the lepidopterous cell, which has
hitherto been known incorrectly as the discoidal cell, but
may be conveniently spoken of as the cell; it of course
includes the median cell when that is present.
While the Comstock-Needham system is, so far as our
170 Dr. A. Jefferis Turner’s Observations on
present knowledge extends, morphologically correct, and
is the only notation which permits of comparison between
the Lepidoptera and. other orders, I am strongly of opinion
that the numerical notation * should be retained for
morphological comparisons within the order, and for these
reasons: (1) it is much simpler and at the same time
absolutely unambiguous, while possessing the advantage
of extreme conciseness; (2) it is free from morphological
theories or assumptions, which however well established
may be lable to future modification. In using it I would
recommend that the origin of the numbered veins be
always given as from the cell or areole, the chorda and
media, when present, being separately described. In con-
sidering the serial morphology of the two wings there is
no doubt as to their correspondence as. far as vein 4, but
the morphology of veins 5, 6, 7, and 8 of the hind-wings
is a matter of interpretation, and subject to correction.
It is, of course, obvious that 8 of the hind-wing does not
correspond to 8 of the fore-wing (a fact that involves no
difficulty if the numerical notation be regarded as a con-
venient form of shorthand). Mr. Tillyard considers 8 of
the hind-wing to be the first radial; I consider it the
subcostal, and identify the first radial with the short vein
marked @ on several of my diagrams. I think Mr. Tillyard
has probably made the mistake of identifying as the sub-
costal a precostal basal spur which is sometimes present
but does not represent any vein, being merely an accessory
process of recent development for the support of a precostal
basal expansion of the hind-wing.
The lepidopterous cell is usually spoken of as closed by
the discocellulars, upper and lower, their junction being at
the median notch. This may be convenient, but it must
be recognised that morphologically the discocellulars are
of complex origin. Their complexity is clearly indicated
in their angulated outline in Culama and other primitive
genera. For instance, in the fore-wing the cell is closed
(1) by a short bar connecting the areole with the first
median; (2) by the diverging bases of the first and second
median; (3) by a short bar connecting the second and
third median and closing the median cell; (4) by the
diverging bases of the third and fourth median; and (5) by
* Sir George Hampson informs me that this was invented by
Herrich-Schi fier,
the Lepidopterous Family Cossidae. 17a
the base of the first cubital before it coalesces with the
fourth median.
Tortricidae.—At first sight the neuration of the fore-wing
of Tortrix, a closed cell from which ten veins arise separ-
ately, appears simple and primitive, and in marked con-
trast with the more complex neuration of the Cossidae.
Nevertheless, if the principles just enunciated are correct,
Fig. 23.—Tortria viridana, Linn.
this simplicity is not primitive but acquired; it originated
from a more complex scheme by a process of loss or astheno-
genesis. It needs but little research to confirm the accuracy
of this anticipation. In many genera both chorda and
median vein are developed, certainly very slenderly but
quite distinctly. The areole is usually narrow, the chorda
running from a little before 10 to just above 7 in Hucosma,
or just opposite 7 in Carpocapsa. The media is unbranched,
Fic. 24.—Kucosma varicgana, Hb. Fie. 25.—Carpocapsa pomonella, Linn.
its exact course through the cell varies, it terminates
between 5 and 6 in Eucosma, just opposite 5 in Carpocapsa.
The media is more rarely distinguishable in the hind-wing,
but a branched media is plainly to be seen in that wing of
Isotrias. In this genus the areole is larger than usual, the
cho da arising shortly after 11 and ending opposite 6,
while the media ends opposite 4. I have not observed a
branched media in the fore-wing in any of the Tortricidae
172 Dr. A. Jefferis Turner’s Observations on
that I have examined. It will be noted that the cell of
Tortriz really represents a compound structure, the com-
bined areole and cell, and I propose to call it an areocel.
Mr. Meyrick in his “ British Lepidoptera” has noted
Fie. 26.—Isotrias hybridana, Hb.
and figured the occasional occurrence of chorda and media
in the Tortricidae. He declares them to be inconstant
and valueless in defining the genera. This may be so,
but they are exceedingly valuable in indicating the true
relationship of the family.
Tineidae-——In this great family
asthenogenesis among the Lepido-
ptera runs to its extreme. In many
of the more minute forms the
neuration is so degraded as not to
be recognisable as of the lepido-
pterous type, were it not that they
are linked to the more typical
forms by intermediate gradations.
These aberrant forms need not
concern us in this essay, for they
are certainly derivative, and the
affinities of a family are entirely
determined by those of its most
primitive genera. The genus Nemophora, with its five-
jointed maxillary palpi and long antennae is certainly
a primitive type, and in spite of its small size preserves a
primitive neuration. In the fore-wing both sector and
media are present, while the hind-wing has a branched
Fig. 27.—Nemophora swam-
merdamella, Linn.
the Lepidopterous Family Cossidae.
media.
173
Cerostoma has an even more primitive neuration
in the fore-wing, the media being branched; but less so in
the hind-wing, the media, although well marked, being
Fic. 28.—Cerostoma
radiatella, Don.
single and running near the costal edge of the cell.
Fig. 29.—Chimabacche
fagella, Fab.
Evi-
dently in this instance it is the lower branch of the media
that is undeveloped.
the chorda and media are,
however, extremely feeble,
though traceable. <A little
further obsolescence would
have resulted in an appar-
ently simple areocel. The
most cossid neuration that
I have found among the
Tineidae oceurs in Titanomis,
Meyr.,* a rather large form
from New Zealand, to which
my attention was directed by
Mr. J. H. Durrant. It is evi-
dently of an early undiffer-
entiated type with all the
veins present and separate.
In Chimabacche the areole is large,
Fic. 30.—Titanomis sisyrota, Meyr.
If we ask ourselves by what
* Nosymna, an equally large form from Borneo, has somewhat
similar neuration with large areole and strongly developed chorda,
but the media is unbranched in both wings.
It has smooth posterior
tibiae as in the Hyponomeutinae, but those of Titanomis are densely
hairy.
Incurvaria pectinea, Haw., has nearly the same structure
as Titanomis, but the chorda and branched media of fore-wings
are very slender, almost vestigial.
174 Dr. A. Jefferis Turner’s Observations on
structural points this genus can be differentiated from
the Cossidae, we can only reply that the chorda and
median veins, though present, are very slenderly developed,
and that there is a well-developed tongue, with distinct
though rudimentary maxillary palpi. In fact, the affinities
of the Cossidae with the M icroleydoptera are so close that
they must be included among them, if the latter term has
any scientific meaning, although the former include the
largest known Lepidoptera, if body bulk is estimated, for
some Australian species of Xyleutes are about as big as a
sparrow. It would be better to acknowledge that Micro-
lepidoptera is not a scientific term and has no more meaning
i.
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Fic. 31.—Cnissostages oleagina, Zel. Fic. 32.—Arrhenophanes perspi-
cilla, Stoll.
than the word Micro-oleoptera. While I am quite unable
to accept Mr. Meyrick’s division of the Cossidae into two
families, he is certainly correct in his opinion as to the true
affinities of the genus Cossus.
The genera Cnissostages and Arrhenophanes, to which
my attention was called by Mr. J. H. Durrant, contain
some large Tineids from South America with curiously
specialised 2 © antennae. In the former there is a small
narrow areole and well-branched median veins in both
wings. In the latter, though an allied genus, the neura-
tion is much less primitive; there is no trace of a chorda,
which suggests that it has disappeared by coalescence and
not by obsolescence, as usual in this family; 9 and 10 are
coincident, and both medians are unbranched.
the Lepidopterous Family Cossidae. 175
Castniadae.—Though this and the three following families
present structures linking ‘hem to the Zeuzeridae, the affinity
is not so close as in the two families I have just dealt with.
In the genus Castnia there is a narrow areole, partly pro-
jecting beyond the cell, the
media with its lower branch is
strongly developed, while the
upper branch «is completely
absent. In the hind-wing the
upper median branch is absent
together with the discocellulars,
except for a short spur arising
from the strongly developed
lower median branch shortly
above the origin of vein 5.
This apparently anomalous
neuration is elucidated in the
diagram by drawing dotted
lines to represent the missing
veins. So far as the fore-wing
is concerned this explanation is
demonstrated to be correct by
the neuration of the genus Gazera, which has a larger
areole, and a media with two long branches. In the
genus Synemon the neuration of the hind-wing agrees
with that of Castnia; the media in the fore-wing is
of the primitive type, but the areole has disappeared,
2?
Fig. 33.—Casinia atymnus, Fab.
Fic. 34.—Gazera linus, Cram. Fic. 35.—Synemon sophia, White.
probably by coalescence of the chorda with the margin of
the cell, so producing the type of neuration characteristic of
the next three families. Before passing on to them I will
draw attention to a peculiarity in the neuration of Gazera,
In the fore-wing of this genus vein 10, which is rather
weakly developed, becomes closely approximated to vein 9.
176 Dr. A. Jefferis Turner’s Observations on
Had these two veins anastomosed they would have formed
a new cell, which might be called a secondary areole.
The importance of this point will become evident later.
Zygaenidae.—In Cyclosia, as in all the genera of this
Fic. 36.—Cyclosia panthona, Cram.
family that I have examined or seen figured, the areole
has disappeared as in Synemon. There is a long-branched
media in the fore-wing, and vein 11 runs into 12, but in
the hind-wing the media is
single as in Chalcosia. Sir
George Hampson figures
Chelura with a_ branched
media in the hind-wing in
his ‘‘ Moths of India,” but
I found it to be unbranched
in all the examples of this
genus examined. I con-
jecture that Sir George
Hampson may have figured
an abnormal specimen.
Chalcosia has vein 11 free,
and the median cell is very
small in the fore-wings. In
the hind-wings the media is
unbranched, and there is
a short oblique vein con-
necting the cell with 8.
Comparing this with the
fore-wing of Cyclosia, we can hardly doubt that this
connection represents one of the missing branches of the
radial in the hind-wing, probably the ‘first radial. The
same vein is present in Zygaena, which has the media
unbranched in both wings, the median cell having been
Fia. 37.—Chalcosia affinis, Guer.
lod
the Lepidopterous Family Cossidae. 177
apparently extinguished by coalescence. In this genus, as
in Procris, the median veins are developed feebly.
From this analysis it will be evident that the Zygaenidae
are less primitive in their neuration than the Cosstdae, and
Fie. 38.—Zygqaena filipendulae, Fria. 39. , (Miresa)
Linn. corones, Fab.
that it is quite impossible that the latter family should
have originated from the former, as maintained by Sir
George Hampson in his * ‘Catalogue of the Lepidoptera
Phalaena” (i, p. 12). This con-
clusion is strengthened, although
such confirmation is unnecessary,
by the absence of tibial spurs in
the former family.
Lnmacodidae.—That this family
is structurally closely allied to
the Zygacnidaz is sufficiently
shown by the accompanying figure
of the neuration of Susica, which
in the absence of the areole and
the structure of the media of fore-
and hind-wings and in other points
agrees closely with Chale sia.
As aless primitive genus [have — Fic. 40.—A poda avellana,
figured Apoda, in which the Linn.
median cell has been lost in both wings. . The short vein
a present in Susica, which I believe to represent the first
radial, is here replaced by a short anastomosis.
At this point we will consider the genus Paracossus,
TRANS. ENT. SOC. LOND. 1918.—PARTS I, II. (DEC.) yw
178 Dr. A. Jefferis Turner’s Observations on
Hmps., which is represented in the British Museum by two
solitary types, P. bare: Hmps., 3, from Ceylon, and
P. furcata, Hmps., 2, from Pegu. They are of somewhat
peculiar facies and ois y similar, but the former has short
porrect palpi, and the latter longer palpi curved upwards
in front of the frons. The tongue is absent. The antennae
in the ¢ are shortly bipectinate to the apex, in the 2
simple, and the posterior tibiae have two pairs of spurs.
The neuration shows no areole, an unbranched media in
both wings, and 7, 8, 9, 10 of fore-wings stalked. Though
this is structurally different from any known Cossidae, I
will not say that it may not
be an aberrant genus of that
family. In Stygia and Inguri-
morpha the media is un-
branched in both wings, and
in Lentagena the areole is so
small that a very small change
would bring about its absence,
and in Acytlara this has
actually happened. But these
genera are connected to the
typical Cossidae by allied inter-
mediate forms, the first be-
longing to a small Palaearctic,
One
; the remainder to a Neotropical
~s z group, while the Oriental Para-
14° cossus stands isolated. Again,
le stalking of 10 with 7, 8, 9
Fia. 41.—Paracossus parva,
Hine does not occur elsewhere in the
Se
family. On the other hand,
the neuration of Paracossus agrees well with that of the
Limacodidae in the unbranched median veins as in Apoda,
and in the stalking of 7 10 as in Susica.
Psychidae. —This family ; 1s age to the Zygaenid group
by the absence of an areole and the development of a
median vein in both wings, as shown in the figure of the
neuration of Clania, which has a branched media with
narrow median cell in both wings. But it also presents
peculiar features in the anal veins of the fore-wing, le
anastomosing with 1b, and la being apparently present.
In the hind-wing there is a short vein emitted from 8 on
its costal side. W hether these are peculiarities developed
in the family, or whether they represent some ancestral
a
the Lepidopterous Family Cossidae. 179
features, are points on which [ am not prepared to express
an opinion without further study.
Pyralidae-—This family need not detain us long. - It
is a dominant group of more modern origin than the
preceding families. In spite
of the frequent presence of
maxillary palpi and the three
anal veins in the hind-wings,
the neuration is of a modern
type without any areole and
usually without any median LZ
veins. In Schoenobius I have 2
observed unbranched median ——
veins slenderly developed in
both wings, and probably
in ly
they would be found in some
other genera if careful search
were made.
We now pass on to the
numerous families which have Wet
only two anal veins in the
hind-wings and one in the
fore-wings. I cannot do more than deal with a few of
these, and that in a summary fashion.
4)
Fia. 42.—Clania variegata, Snell.
Fic. 43.—Dudgeona actinias, Turn. Fie. 44.—Phragmatoecia castanede,
Abnormal neuration. Compare Hb. Abnormal neuration.
ne ‘ ys
Fig. 2. Compare Fig. 11.
Lasiocampidae.—This family, however, deserves rather
fuller treatment. I have already pointed out that the
areole may be lost in two ways, by obsolescence of the
chorda, or by coalescence of the chorda with the common
stalk of the second and third radials. There is yet a third
way. As already mentioned in one example of Dudgeona
180 Dr. A. Jefferis Turner’s Observations on
actinias (fig. 43), the bar between 8 and 9 which completes
the areole is undeveloped. Similarly in an example of
Phiagmatoecia castaneae (fig. 44) the usual anastomosis
between 8 and 9 is absent. In both these instances the
areole has coalesced with the discal area outside the lepido-
pterous cell. These abnormalities illustrate, I believe, the
normal structure of the Lasiocampidae. In the figure of
Lasiocampa the letters ar mark the site of the undeveloped
areole. There is a small cell with a slenderly developed
unbranched media, and this cell is, I believe, the primitive
lepidopterous cell, not an areocel, as in all the preceding
Ly 18
1c. 45.—Lasiocampa quercus, Linn. Fre. 46.—Bhima undulosa, Wik.
famihes which lack an areole. This separation of 8 and 9
of course leaves the veins 9 and 10 stalked. But when an
areocel is formed, as may be seen at a glance at any oi
the figures up to fig. 42, 9 and 10 are left arising separately
from it. Usually 9 is attracted to 8, the instances in
which it becomes again stalked with 10 are rare and excep-
tional; but in the Lasiocampidae 9 and 10 are invariably
stalked. In the Indian genus Bhima the ancient structure
is obscured by the stalking of 8, 9, 10, but this is a rare
and late modification; in the great majority of genera 8
is separate or stalked with 7. But Bhima has one primi-
tive character in the retention of lc of the fore-wings. The
hind-wings of the Lasiocam pidae usually differ very much
the Lepidopterous Family Cossidae. 181
from those of the other families dealt with in this pa per. The
cell is small, without any media, 7 arises from its costal
edge rather near the base and is connected with 8 by a short
oblique vein a as in Lasiocampa, or by an anastomosis as in
Bhima. regard the former as more primitive. The offshoots
from 8 are not veins, but chitinous thickenings developed to
strengthen the precostal expansion of the hind- -wing, which
compensates for the absence of a frenulum in this family.
In an undescribed genus from West Australia, for which I
propose the name N eurochyta,* the fore-wing differs from
Lasiocampa only in the stalking of 7 and 8, and the absence
of the media. The hind-wings are very exceptional in
the family in the origin of 7
from very near the end of
the cell, as is usual in other
families, and the cell is of the
normal lepidopterous form. I
regard this as a fortunate
discovery in preventing me
from attaching too much im-
portance to the peculiarly
formed hind-wing cell usual in
the Lasvocampidae, and as in-
dicating, by the preservation
of a more primitive form, how
it may have developed. Yet
Neurochyta has a lasiocampid
hind- wing, for 8 anastomoses Fia.47.—Neurochyta edna, Swinh.
strongly with the cell near the
base, and though the pre-costal cell so formed is very
small, it gives rise to two strong branching spurs or
pseudoneutia.
There seems, therefore, no real difficulty in deriving the
Lasiocampidae from the cossid stem, although it is an
isolated and early development from it.
* Neurochyta, gen. nov. Palpi moderately long, porrect, reach-
ing beyond frontal tuft, densely hairy. Fore-wings with 2 from 4,
3 from 3, 4 and 5 approximated from angle, 6 from upper angle
connate with 7, 8 which are short-stalked, or 6, 7, 8 stalked, 9, 10
stalked, 11 from 2, free, but running close under 12. Hind-wings
with 2 from middle of cell, 3 from shortly before angle, 4, 5 stalked
from angle, 6 from upper angle, 7 from shortly before angle, 8
anastomosing with cell from near base to 4, precostal cell minute,
two precostal pseudoneuria arising together near base and diverging.
Type NV. edna, Swinh.
182 Dr. A. Jefferis Turner’s Observations on
Noctuidae, Arctiadae, Liparidae, Notodontidae-—We will
consider these four families together. I have picked out
one genus from each showing a well-marked areole and
chorda of typically cossid form. I see no reason to doubt
that it is actually a primitive areole. A secondary areole
not homologous with the primitive areole is a possibility,
y=
Fia. 48.—Agrotis pronuba, Linn. Fia. 49.—Palacosia bicosta, Wik.
as I have pointed out when describing the neuration of
Gazera, one of the Castnmiadae, and if such a structure was
formed in a genus, in which areole and cell had coalesced
to form an areocel, it might even be impossible to dis-
Fie. 50.—Orgyia mendosa, Hb. Fria. 51.—Gargetta costigera, W1k.
tinguish it by inspection from a primitive areole, although
morphologically of different origin. But there are two
strong reasons for believing that this has not occurred
in the Noctuidae, Wrciadoe Liparidae, and Notodontidae :
(1) in these families there are genera which demonstrate
the gradual obliteration of the areole by coalescence, but
no genera exist in which there is any approach to the
the Lepidopterous Family Cossidae. 183
formation of an areole; (2) the areole exists in the more
primitive genera of the four families, and there is good
reason for holding that the genera which have no areole
have descended from forms which once possessed it. In
the Noctuidae the neuration is remarkably constant. As
Sir George Hampson informs me, the ‘typical noctuid
neuration, as illustrated in Agrotis, 1s present in the vast
ma‘ority of the genera, and in those that do not possess it
Fra. 52.—Thyatira batis, Linn.
it has been lost* (see Introduction to * Cat. Lep. Phal.,” vols.
iv and x). In the other three families there is more vari-
ability, and it would take a much more lengthy examina-
tion than I can afford at present to prove that the forms
which possess an areole are the more primitive. I can
only express my belief that it 1S SO.
While in the Zygaenidae, Limacodrdae, and Psychidae
* The primitive genus Hyblaea which possesses maxillary palpi
has, however, lost the areole and cannot therefore be in the primi-
tive noctuid stem, but must be an early branch from it.
184 Dr. A. Jefferis Turner’s Observations on
the cossid areole and chorda have been lost, but the media
has been retained, in the Noctuidae, Arctiadae, Liparidae,
and Notodontidae the former have been retained and the
latter lost. It follows that the descent of the second group
of families from the first is an impossibility; they have
developed from the cossid stem by a separate branch.
How far this applies to those families which have lost both
structures I will not inquire at present. It is advisable,
however, to note that although the media is not developed
as a vein, which occurs rarely i in the higher families, it is
frequently represented, either branched or unbranched, by
Brees:
Monoctenia falernaria, Fic. 54.—Diceratucha
Gn. xenopis, Low.
a fold in the wing-membrane. These folds I have not
reproduced in my diagrams.
Thyatiridae (Cymatophoridae).—The explanation that I
have given as to the fate of the areole in the Lasiocampidae
is to some extent supporied by the analogous structure in
the Thyatiridae. As Sir George Hampson “has pointed out,
the areole in this family is frequently not closed, the varia-
tion occurring rather frequently in the limits of a single
species. There does not appear to be here any instance
of the development of a new structure, which would be
shown by a gradual change in a series of related genera,
but of the loss of part of a structure in a proportion of
individuals of a species perhaps owing to the absence of
the Lepidopterous Family Cossidae. 135%
some Mendelian factor. This curious variation is illus-
trated in the figure of Thyatira batis, Linn. The hind-wing
shows some similarity to that of the Lasiocampidae, 7
arises from well before the angle of the cell, and, although
there is no anastomosis, 8 is approximated to 7, but there
is a well-developed frenulum, and I do not think the
similarity points to any real community of descent. Whether
the areole is really a primary and not a secondary areole in
this family is not quite certain, but I think the former is
more probable.
Geometridae.—This large family affords very interesting
studies in neuration. By neuration alone 1t may be divided
into at least five perfectly natural subfamilies. I have
figured two of the most primitive genera in the most
primitive subfamily Monoctenianae. They show remark-
able differences. In Monoctenia there is a slender but
Fie. 55.—Bupalus piniarus, Linn.
distinct branched media in both wings, the areole being
absent. In the three Australian genera Diceratucha, Dirce,
and Xenogenes the media has been lost, but a large areole
and well-marked chorda retained. These are very primi-
tive genera, and I have no doubt this is a primitive areole,
which in most of the family has been lost. It so happens
that veins 10 and 11, which arise from the areocel separ-
ately and remain free in Monoctenia, often vary remark-
ably, not only in allied genera but in the same genus, and
often in different individuals of the same species. This is
especially the case in the subfamily Boarmianae. Here
10 and 11 may be separate or stalked at origin, and there
is a strong tendency for 11 to anastomose with 12 and 10
with 9. In Bupalus 11 runs into 12 and 10 anastomoses
with 9 to form a secondary areole, which has no relation-
ship to the areole present in Diceratucha. In the Geome-
trinae 10 is usually stalked with 9 and there is a tendency
for 11 to anastomose first with 12 and then with 10, but
186 Dr. A. Jefferis Turner’s Observations on
an areole is never formed. In the Acidalianae, on the
other hand, an areole is present in most genera, and those
that do not possess it have lost it, the stages of its loss
being often still preserved. The Acidalianae are a
specialised, not a primitive subfamily, and their areole is
evidently a secondary one. Similarly the Larentianae have
nearly always a secondary areole, originally double, but
with its internal partition often not developed, formed by
an anastomosis of 11 with 10, and of 10 with 9.*
Fig. 56.—ELois aversata, Linn. Fie. 57.—Hydriomena dotata, Linn.
CONCLUSION.
To sum up the results obtained by this inquiry. All
the Lepidoptera Heteroneura are descended from a group
with cossid neuration, to which, for convenience, I will
give the name Protocossidae. The Protocossidae possessed
a spiral proboscis or tongue with at least rudimentary
maxillary palpi;+ it had well-developed labial palpi,
porrect or ascending; the tibial spurs were long and all
present. The neuration of the fore-wing was that of
Zeuzera, except that all the veins from the areole arose
separately as in Macrocyttara. The neuration of the hind-
wing was that of Xyleutes, except that a short oblique
vein connected the cell with 8 as in Xystus. Perhaps the
nearest living genus to the Protocossidae is Titanomis, a
primitive Tineid, and from a form resembling this have
descended the Tortricidae and a very large proportion, if
not all,+ of the Zineidae. From the Protocossidae arose
* These conclusions may possibly be modified by a more ex-
haustive study of the family than I am able to give to it at present.
+ Kither the Protocossidae had five-jointed maxillary palpi, or
those Tineidae which possess them, together with their immediate
allies, descended from the heteroneurous trunk by a separate stem
at an earlier level, and the Tineidae contain the descendants of two
separate lines of descent approximated by convergence,
the Lepidopterous Family Cossidae. 187
also (1) the Castniadae by a separate stem; (2) the Zygae-
midae, Limacodidae, Psychidae, and Pyralidae, the first two
from a common stem, the exact relationship of the last
two being less certain; (3) the Lasiocampidae by a very
distinct stem; (4) by yet another stem the Noctuidae,
Arctiadae, Liparidae, and Notodontidae, together probably
with the Geometridae and Thyatiridae. If so much be
admitted, we have already a classification in outline of
the Heteroneura. The assignment of the other families of
this great assemblage to their positions within this outline
must be reserved for another occasion.
It is apparent that this
phylogeny is based mainly
on the neuration. No one
is more anxious than I to
consider all the characters
of all the stages of the
Lepidoptera, but the value
of all the characters must
be carefully weighed. The
great problem of phylogeny
is the distinguishing of
resemblances due to com-
munity of descent from
those due to evolution in
a common direction usually
but perhaps not always
under the influence of the
environment, that is to
say, to adaptation to com- Fig. 58.—Neuration of the hypo-
mon conditions. Or, as thetical family Protocossidae.
my old teacher, Prof. Ray
Lankester, used to say in his lectures, we must distinguish
homogeny from homoplasy. No better illustration of homo-
plastic resemblances can be found than among the larvae
of Lepidoptera, for instance, in the resemblance of some
Noctuid larvae to those of the Geometridae, of other Noctuid
larvae to those of the Bombycine families. Lepidopterous
larvae are peculiarly exposed to adaptational modification,
They are in no sense embryonic forms, that is to say,
forms recapitulating the phylogeny of the insect, but
secondary adaptations to a phytophagous existence depart-
ing more widely from the primitive insect than do the
imagines, and morphologically much degraded, Their
188 Dr. A. Jefferis Turner’s Observations on
characters within the various families have sometimes
considerable phylogenetic value, but little value in indi-
cating the true relationship between the families. To
attempt a classification of the Lepidoptera from the relative
position of the tubercles on the larval skin, as has been
done by Mr. Dyar, seems to me as profitless as it would
be to classify the whole order by the form of the palpi,
or the shape of the outlines of the wings in the perfect
insect.
The pupal and oval characters advanced by Dr. Chapman
appear to me to stand on a better foundation. I am quite
ready to admit that forms with a greater number of mov-
able pupal rings, his Incompletae, are more primitive than
those with fewer movable rings, his Obtectae; but this does
not carry us far. It seems probable also that the dis-
tinction between forms with vertical eggs having a central
micropyle from those with flat eggs in w vhich the. micropyle
is on the side may have important phylogenetic signifi-
cance. In the former group are the four families Arctiadae
(from which arose the Syntomidae), Noctuidae, Liparidae
(with which I associate the Hypsidae) and Notodontidae,
families which, it will be observed, I have associated on
neurational characters. The only other family with upright
eggs, excepting those usually known as Rhopalocera, whose
origin I am not at present prepared to discuss, are the
Castniadae, and these I regard as an isolated group. In
the Cossidae the oval characters appear to have remained
in a fluid state, for Dr. Chapman states (Trans. Ent. Soc.
1896, p. 579) that while Cossus has a vertical egg, that of
Zeuzera is flat. If this is so it is admissible to assume
that the same held true of the Protocossidae, and that these
have given origin not only to the above-mentioned families
with vertical egos, but to other families in which the eggs
are always flat.
The neuration is by far the best guide to lepidopterous
phylogeny that we possess; it is a hidden structure pro-
tected from the direct action of outside influences to a
large extent, rarely affected by directly adaptational
changes, and, in short, the best field in which to search
for homogeny unobscured by homoplasy. Yet even here
homoplastic influences are at work, and cautious interpre-
tation is necessary, for there is a widespread tendency in
many different families towards a simplification of the
neuration, which often proceeds along parallel lines.
the Lepidopterous Fanuly Cossidae. 189
The Lepidoptera have specialised in colour and wing-
pattern, not in structure. The great achievement of the
order in structure was the development from the maxillae
of the spiral proboscis, and this happened long since.
Among existing families structural evolution has had but
trivial results, consisting (I am writing, of course, of the
imagos) of little more than secondary sexual characters.*
On the other hand, there has been a strong tendency in
nearly all the families to progressive reduction in structural
complexity, to a progressive simplification by structural
loss, on parallel lines. Unless this is fully recognised
no progress will be attained in the true phylogeny of
the different groups. I will enumerate some of these
lines, and point out how remarkably they have been
followed even within the very ancient and primitive
Cossidae.
(1) The proboscis and maxillary palpi have been lost in
the Cossidae, Psychidae (only the 3 can be brought into
comparison, the 2 being degraded to an extreme degree),
Limacodidae, Lasiocampidae, Liparidae, and in other whole
families, as well as in many isolated genera.
(2) The labial palpi have been lost in some genera of
Cossidae and quite independently in many genera of other
families.
(3) The tibial spurs have been lost or much reduced in
most Cossidae, in the Zygaenidae, Psychidae 3, and in
other instances.
(4) The frenulum has become shortened and non-
functional in a few Cossidae, wholly lost in all the Lasvo-
campidae, Endromidae, Uranianae, and in some genera of
the Drepanidae, and Bombycidae and the Geometrinae
subfamily of the Geometridae; in the last instance every
grade between full development and complete loss can
still be traced.
(5) The median vein is always present in the Cossiae,
but in a few genera, the first step in its obsolescence, the
obliteration of the median cell has taken place. It is
completely lost or merely vestigial in most Lepidoptera.
(6) The areole and chorda are lost in at least one genus
of Cossidae, in all genera of most other families, and in
those families that retain it, it has been lost in some, if not
* T leave out of consideration the basal abdominal cavities, as
to which I have no precise knowledge.
190 Dr. A. Jefferis Turner’s Observations on Cossidae.
most, of the genera. This is a striking instance of parallel
involution in “independent groups.
(7) The peripheral veins are partly or wholly coalesced
to some extent in nearly all families. In the Cossidae this
does not proceed beyond partial coalescence (stalking).
Other instances might be mentioned, but these are
sufficient.
( 191 +)
X. The charina Group of Pinacopteryx. By F. A. Dixry,
M.A., M.D., F.R.S., Subwarden of Wadham College,
Oxford.
[Read May Ist, 1918.]
Tue assemblage of Pierine species including cebron and
capricornus, Ward, pigea and charina, Boisd., with others
nearly related to them, forms a natural group which may
either be considered as a separate genus under the name
of Pinacopteryx, or as a section of Pieris in the wide sense ;
the latter course being taken by Trimen in “* South African
Butterflies,” vol. iii, p. 39; and by Aurivillus in Seitz’s
‘“ Macrolepidoptera : Ethiopian Region,” Eng. trans., p. 45.
In Proc. Ent. Soc. Lond., 1912, pp. ex—-cxiv, it was
remarked that the group headed by P. charina was distinct
in several particulars from the remainder of the section or
genus, and in the same ‘* Proceedings ” for 1909, pp. cLx, ex,
some account was given of the peculiarities of the scent-
scales which characterise this charina group; an outline
figure being added of the curious plume-scale of P. liana,
Gr. Smith (Jbid., Pl. E, fig. 10). I now propose to deal
in somewhat greater detail with the members of this sec-
tion, as regards which there has been a certain amount of
confusion.
The charina group, as has been pointed out by Auri-
villius,* is distinguished from the remaining species of
Pinacopteryx, which may be called for convenience the
pigea group, by the possession on the lower discocellular
vein of both wings, or at least of one wing, of a black
spot or dot beneath, often occurring on the upper surface
also. This, though in practice a useful distinction, does
not invariably hold good; for in one or two forms of the
pigea section a dot may be present in the assigned situa-
tion, and in one form at least of the charina section both
surfaces of both wings may be devoid of any such marking.
A more constant distinction, so far as the males are
concerned, is afforded by the genitalia.t In all the species
* Op. cit., p: 46.
+ This, I believe, was first observed by my friend Dr. H.
Eltringham.
TRANS. ENT. SOC. LOND. 1918.—PARTS I, Il. (DEC.)
192 Dr. F. A. Dixey on
of the pigea group, the clasper ends posteriorly in two
spinous prolongations, one placed dorsally to the other
(fig. 1). These are usually very well marked; but in one
species, viz. P. spilleri, Stdgr., they are exceptionally short,
though still easily visible. In the
charina group the clasper is furnished
posteriorly with only one spine instead
of two (fig. 2).
The members of this latter group
are probably best regarded as a single
species including several geographical
forms of subspecific rank. The form
which is most distinctly marked off
from the rest would seem to be
charina itself. This was described by
——. Boisduval from males and females
captured in Kaffraria. Aurivillus in
Fra. 1.—P. orbona, Seitz, loc. cit., gives the distribution
Hiibn. Doubled spine ae Byte : {
of clasper X 54. of charina as “* South Africa to German
Kast Africa,’ but I have not seen any
specimens of this southern subspecies from further north than
the Transvaal. Another form which seems to be easily dis-
tinguishable is that described by Grose Smith * as Belenois
Fic. 2.—P. charina, Boisd. Single spine of clasper x 54.
liana, and figured by Grose Smith and Kirby + as Pina-
copleryx liliana. The locality given by the describer is
Mombasa, and the same form is found in the surrounding
region at least as far to the west and north as Taveta and
* Ann. Mag. Nat. Hist., Series 6, vol. 3, p. 122 (1889).
{t Rhop. Exot., Pinacopteryx, Pl. I, figs. 7, 8 (3), 9 (9).
the charina Group of Pinacopleryz. 193
Machakos. Pinacopteryx gerda, figured and described by
Grose Smith and Kirby (loc. cit., “figs. 10, 11), also from
Mombasa, is probably a male of P. Liliana somewhat smaller
than the average and less heavily marked with black.
Specimens from the Voi River, the Tana River and Mlegwa
all in British East Africa, correspond in appearance with
Pinacopteryx gerda.
There remain certain forms, allied to the foregoing and
to each other, which have been known under the names of
P. doxo, Godt., P. simana, Hopfi., and P. venata, Butl.
P. doxo was the first member to be noticed of the whole
charina group. It was described by Godart * in 1819 as
Pieris dovo. Godart’s type is in the Dufresne Collection,
now at Edinburgh, and has been figured by MnP. Grimshaw
in Trans. Roy. Soc. Edin., vol. xxxix, Pl. I, fig. 6 (1900).
It is a female in somewhat poor condition. The locality
is left blank by Godart ; but Boisduval,+ who reproduces
Godart’s description, says, “ Afrique probablement.” A
careful examination of the type specimen makes it tolerably
clear that it is a Pinacopteryx of the group at present
under discussion, though it is by no means easy to assign
it to its proper place among the forms included in that
section. On the whole I should be disposed to agree with
Aurivillius (loc. cit., p. 46) that it belongs to the form
afterwards described by Hopfier as Pieris simana (types
from Mozambique), were it not improbable that any of
Dufresne’s collection came from that region. As the case
stands, I suspect that Godart’s type may be really a some-
what unusual example of the wet-season form of P. charina
from the region of the Cape. It is, however, not exactly
like any Pinacopter yx that I have ever seen, and it differs
considerably from the figure of “ doxo 2.” in Seitz, op. cit.,
Pl XIV, ec. This figure, indeed, probably represents a
dry-season female of Grose Smith’s liliana, and was certainly
not drawn from Godart’s type.
The type of P. dovo thus being a battered female of
unknown locality, its determination is so uncertain a
matter that I venture to think it best to drop the name
altogether as a specific or subspecific designation. The
next question to arise is that of the relation of P. semana
to P. venata. Butler’s type of P. venata, a female, came
from the White Nile; it was described and figured by him
* Enc. Méth., ix, Ey 123, 5.
7 Sp. Gén., I, p. 527, n. 130 caeta
TRANS. ENT. SOC. LOND. 1918.—PARTS Li «(DEC.) 0
194 Dr. F. A. Dixey on
in Trans. Ent. Soc. Lond., 1871, p. 169, Pl. VII, fig. 7,
Ixias venatus. The male of this form was unknown until
1902, when Mr. Loat captured one at Gondokoro; this
was described in Trans. Ent. Soc. Lond., 1903, p. 152
The male type and a female from Shambi on the White
Nile were well figured by Dr. Longstaff.* P. simana, as
already stated, was described by Hopfier from } Mozambique.
Both sexes are figured by Peters.* The name venata is
not inappropriate. to Butler's type, which is somewhat
heavily marked, and has the veins accentuated with black.
In many other female specimens (probably of the dry
season), and in all the males with which I am acquainted,
the black veining is absent from the upper surface. In
P. simana, on the other hand, although the females vary
in this respect, probably, like those of P. venata, according
re
Fic. 3.—P. liliana, Gr. Smith. Spine of clasper x 54.
to season, the males appear always to have the veins
on the upper surface more or less marked out with black.
On these and other grounds presently to be mentioned,
I think that simana and venata, though no doubt closely
allied, are separable as subspecies.
It may then be said, at least provisionally, that there
are four, or perhaps five, subspecies which can be ranked
under the head of Pinacopleryx charina. It will be of
interest to see what light can be thrown on the mutual
relations of these forms by an examination of structural
details.
(1) The Male Genitalia—As already remarked, the
clasper in all these forms ends posteriorly in a single
spinous projection. This in a specimen of P. liliana from
Mombasa is long and slender (fig. 3). In an example of
* Trans. Ent. Soc. Lond., 1913, Pl. II, figs. 1,.2, 3.
+ Reise nach Mossambique, Taf. X XIII, figs. 3-6.
the charina Group of Pinacopteryz. 195
P. charina from Weenen, Natal (fig. 2), it is also long,
but markedly less so than in P. liliana. The terminal
spine in a P. siumana from Gazaland (fig. 4) and a P. venata
from Gondokoro, White Nile (fig. 5), is short; it is some-
what blunter in semana than in venata. A point to be
noted is that, judging from these examples, the clasper of
charina, a comparatively small form, is not much less in
size than that of hana, decidedly a larger insect. The
claspers of semana and venata are much smaller. In all
four forms the terminal spine is furnished at its free ex-
tremity with a socket from which proceeds a group of
chitinous bristles. These are not represented in the figures.
The socket is indicated at s.
Fic. 4.—P. simana, Hopf. Fig. 5.—P. venata, Butl. Spine of
Spine of clasper x 54. clasper x 54.
There is also a difference to be observed between the
two sections of Pinacopteryx, in reference to the character
of the uncus. This structure in the charina group is com-
paratively slender, and rather sharply pointed. The dorsal
margin is slightly sinuous in outline, and the distal portion
of the uncus is curved downwards, sometimes so decidedly
as to give the organ almost a sickle-shaped character
(fig. 7). In the pigea group, on the other hand, the dorso-
ventral dimension is proportionately greater, the free
extremity 1s comparatively blunt, the dorsal margin is
uniformly convex, and the curve of the organ, though
present, is less pronounced (fig. 6).
(2) The Scent-scales.—These, as elsewhere noted, present
196 Dr. F. A. Dixey on
in all the forms the general appearance of an elongated
lamina with rounded base and parallel sides. In specimens
of P. liliana from Mombasa, Taveta, the Dabida Hills,
Thiba River and near Machakos, the rounded base is
J
Fic. 6.—P. pigea, Boisd. Uncus x 54.
Tic. 7.—P. gerda, Gr. Sm. and Kirb. Uncus x 54.
greatly expanded and takes up by far the greater part of
the area of the lamina. The outline of the scale thus
becomes flask-shaped, the neck of the flask being repre-
sented by the portion of the lamina distal to the basal
if expansion (fig. 8). The scent-scales of
NI? a male specimen from Mombasa which
corresponds with the description and
figure of P. gerda by Grose Smith and
Kirby, exhibit precisely the same char-
acters as the foregoing. This appears
to favour the impression that the only
difference between gerda and liliana is
one of season. The specimens above
referred to (p. 193) from the Voi River
and Mlegwa closely resemble in aspect
the gerda” from Mombasa; their scent-
Fia. 8—P. liliana, scales, however, present a_ different
ae ey ea appearance, the basal expansion being
p, Searels patch, much reduced (fig. 9). So far as outline
goes, they are much like the corre-
sponding structures in P. simana, but they possess one
character in common with P. liana which is not ‘shared
by simana; and which, in conjunction with another
feature presently to be mentioned, seems to indicate
the charina Group of Pinacopteryz. 197
that these Voi River specimens may be regarded as
a slightly divergent form of P. liana. Whether Smith
and Kirby’s name of gerda may properly be applied to
them is perhaps open to question. The character of the
scent-scale just alluded to is the occurrence,
at or near the junction of the neck with
the body of the flask, of a rough-looking
eranular patch, dark by transmitted light,
most conspicuous in Liliana from Mombasa,
but easily recognisable in the gerda-like
specimens above mentioned (figs. 8, 9, 7).
This appearance is not seen in the scent-
scales of charina, simana or venata; a
diffused shading, but no definite granular ’
patch, being the nearest approach visible Fic. 9.—P. gerda,
in the corresponding situation. a ie
When I first investigated the scent- scala se S10
scales in this group, working with some- —P granular
what limited material, I formed the on
opinion that P. venata could be easily distinguished from
P. simana by the shorter and broader character of its
scent-scales.* This was the case with the specimens from
which my preparations were made; but the examination
of additional examples has shown that the distinction does
A 7
i
Fig. 10. Fig. 11, Fig. 12.
Fic. 10.—P. charina. Boisd. Scent-scale x 310.
Fic. 11.—P. simana, Hopff. Scent-scale x 310.
Fic. 12.—P. venata, Butl. Scent-scale x 310.
not universally hold good. It occasionally, though rarely,
happens that a scent-scale from an undoubted specimen
of P. venata (as in one from Hagarat in South Kordofan)
is as long as an exceptionally short scale from P. simana;
and similarly, a scale here and there from P. venata (as
* Proc, Ent, Soc, Lond., 1912, p. exiii.
198 Dr. F. A. Dixey on
in a specimen from Gondokoro on the White Nile) is
narrower in proportion than the usual scale of P. simana.,
But there is no doubt that a comparison of the average
dimensions of the scent-scales in the two forms shows the
distinction above stated. The scent-scale in P. charina is
much like that in P. semana, but here again it is on the
average shorter, though not so short as that of P. venala
(hes: 10s 1112).
It was mentioned on p. 196 that in addition to the dark
eranular patch of the scent-scale, there was another feature
which would seem to indicate that the Voi River and Mlegwa
specimens are a form of liliana rather than of simana.
This is the presence of a well-marked dark spot on the
upper surface of the fore-wing of the female, situated
between the median and submedian veins and usually
extending into the space below the submedian. The spot
in question is characteristic of the wet-season and inter-
mediate females of [iliana, including the “ gerda”’ form
from Mlegwa and the Voi River, but appears to be always
absent, or at most only represented by a very slight
powdering of dark scales, in the females of charina, simana
and venata. Judged by this criterion, as well as by the
evidence of the scent-scales, there appears to be no doubt
that the “ gerda”’ forms are rightly associated with liliana
and not with semana.
It may be well here to recapitulate in some detail the*chief
points that call for notice in regard to these several forms.
(1) P. charina, Boisd.—This is the form which is found
in Cape Colony, Natal, Zululand, and (probably) the
Transvaal. Both males and females are without black
veining. The male is nearly always without any dis-
cocellular spot on the upper surface, but possesses one on
the lower surface of the hind-wing, and occasionally of
the fore-wing; the latter, if present, being minute. On
the upper surface of the fore-wing of the female the dis-
cocellular spot may be present. or absent; it appears to
be always absent from the hind-wing. Beneath, in the
female, it is constantly present in the hind-wing and often
visible on the fore-wing as well. The upper surface of
the male may be entirely immaculate; but on the fore-
wing there is usually a dark streak bounding the costa,
and a marginal series of dots on the hind border, which
are often discrete, but may be merged into a dark band
the charina Group of Pinacoplerys. 199
never very broad. A similar marginal band in the female
is usually broader and better marked, but may be almost
obsolete. The female has a chain of subapical spots on
the fore-wing, reaching from the costa to the space below
the first radial branch; a larger spot occupies the space
between the second and third median; this is usually
isolated, but a minute spot sometimes occurs below the
second radial, completing the chain. Both sexes show a
pearly lustre at the base of the wings on the upper surface ;
this extends over a larger area in the female than in the
male. The under surface of the hind-wing and apical area
of the fore-wing are pale yellow, marked in the dry-season
form of both sexes with a rich irroration of dark specks
or blotches; the submarginal spots of the female are
visible beneath, being more or less assimilated to the
irroration. The male has occasionally on the underside
an indication of the costal end of a corresponding sub-
marginal chain; but from this sex the spot between the
second and third branches of the median is nearly always
absent, though it may be present in the wet-season form
as a small dot. In the wet season also the irroration
becomes reduced to a series of small submarginal spots,
sometimes very faintly marked. In both sexes the veins
of the hind-wings on the upper surface and. both wings
of the lower surface may possess minute marginal dark
dots. These may be present at all seasons. The male
clasper in a specimen from Natal is larger than in P. semana
and P. venata; it resembles that of P. liliana in size
and in the length of the single posterior spine (fig. 2),
which is nearly as long as in that subspecies. The uncus
(fig. 13) is small relatively to the size of the clasper. The
lamina of the scent-scale has parallel sides and an ex-
panded and rounded base. In size it is intermediate
between those of P. simana and P. venata.
(2) P. simana, Hopft.—This is the form found in Por-
tuguese and German Hast Africa, Rhodesia, British Central
Africa, Uganda and British East Africa with the exception
of the coast region about Mombasa, where it is replaced
by P. liliana and P. gerda. In this subspecies the male is
invariably veined on the upper surface, more distinctly so
in the wet than in the dry season. In both sexes the dark
border of the fore-wing is continuous, showing little ten-
dency to break up, as in charina, into a series of marginal
spots. In both wet- and dry-season phases of the female
200 Dr. F. A. Dixey on
there is a strong tendency for the apical portion of the
dark border to fuse with the submarginal series of dark
spots, thus forming a well-marked apical patch. A small
discocellular spot may be present on the fore-wing of the
male, especially in specimens from west of Lake Victoria
Nvanza, but only in rare instances on the hind-wing. A
similar discocellular spot is always present on the “fore-
wing of the female, and in the wet-season form on the
hind-wing as well. Very rarely there may be in the
female a slight indication of a dark spot in the space
between the median and submedian veins of the fore-
wing; this is shown in the figure of the type in Peters’
Reise.* Beneath, the general surface of both wings in
the wet-season male is white with more or less dark vein-
ing; this veining in a series of males from west of the
Victoria Nyanza is extremely well marked, especially on
the hind-wing. A submarginal series of spots is more or
less visible on both fore- and hind-wing. These in the
series last referred to are highly developed, and are fre-
quently united into a conspicuous submarginal band,
which, however, in the fore-wing does not extend further
backward than the space between the second and third
median branches. The discocellular spots are always
present on both fore- and hind-wings. The underside of
the wet-season female varies a good deal according to
locality. The hind-wing and apex of fore-wing are usually
yellow; the remainder of the fore-wing, white. The sub-
marginal spot between the second and third median is
always conspicuous, the rest of the submarginal series may
disappear. There is, however, nearly always a submarginal
chain visible on the hind-wing, and in females from ‘west
of the Victoria Nyanza the submarginal band is as well
developed on both wings as that of the males from the
same region. The discocellular spots are always present,
as in the male. In the dry season the hind-wing and
apical area of the fore-wing in both sexes become over-
spread by a brownish irroration, with which the dark
markings become assimilated. The powdering is usually
more blurred and of a paler brown than in charina; the
discocellular spots, as above noted, are present in both
sexes. The clasper in a male from Gazaland is small;
its posterior spine (fig. 4) is blunt, not prolonged as in
* Reise nach Mossambique, Taf. X XIU, figs. 5, 6.
the charina Group of Pinacopteryz. 201
charina. The uncus (fig. 14) is abruptly curved at: its
distal end. It bears some resemblance in outline to the
upper mandible of the beak of a gull. The scent-scale
(fig. 11) is like that of charina, but generally longer.
(3) P. liliana, Grose Smith.—This is a_ well-marked
subspecies from Mombasa and the adjacent region, in-
cluding Taveta and Machakos. It is on the average con-
siderably larger than any of the other forms of the charina
group. The wet-season male is veined with black on the
upper surface, and is somewhat heavily marked with grey
on the inner half of the costa of the fore-wing and the base
of both wings. The apex and posterior margin of the fore-
wing are margined with black. There are no discocellular
spots on either wing. The wet-season female may be either
white or yellow on the upper surface; it has a broad dark
Fic. 13.—P. charina, Boisd. Fig. 14.—P. simana, Hopft.
Uncus x 54. Uneus x 54.
Fic. 15.—P. venata, Butl. Uncus x 54.
border to the fore-wing, with which the costal part of a
submarginal chain is usually merged. The hind-wing is
bordered by a series of large dark spots, sometimes fused
together. The submarginal spot between the second and
third median branches is very large and conspicuous; and
there is always visible a spot, belonging to the same series,
in the space between the median and “submedian, usually
passing the boundary of the latter vein. A submarginal
band or row of spots is sometimes visible on the hind-wing.
A discocellular spot is always present on the fore-wing,
and usually on the hind-wing also. Beneath, the wet-
season male is white with small dark marginal dots and a
chain of submarginal brownish spots, more or less developed,
on both fore- and hind-wings. Discocellular spots are present
on both wings, and there is a large and conspicuous
submarginal spot between the second and third median
202 Dr. F. A. Dixey on
branches, occupying the same position as in the female.
In the wet-season female the costa and apex of the fore-
wing and the whole of the hind-wing are usually yellowish
beneath. The submarginal chain of spots is present on
both wings; the spot on the fore-wing between the second
and third median being large and conspicuous, as on the
upper surface. Discocellular spots are present on both
wings. In the dry season the male may show above little
or no trace of dark veining. The dark markings of the
female are also much reduced, but the large spot between
the second and third median branches is still present and
conspicuous on the fore-wing; the hind-wing may be
spotless, though there is usually a marginal series of dark
spots, A discocellular spot is generally present on the
ad
Fic. 16.—P. liliana, Gr. Smith. Spine of clasper x 54.
fore-wing, but not on the hind-wing. Beneath, the male
may be spotless but for the large median spot, which per-
sists. The female often shows a slight mottling on the
hind-wing and apex of the fore-wing, to which the sub-
marginal spots are assimilated. This mottling is com-
paratively pale, and the powdering specks are usually
more sparsely distributed than in most specimens of
P. charina. Discocellular spots are present on both wings,
but may be very faint. The clasper in a male from Mom-
basa is large, like that of P. charina; and ends posteriorly
in a long spur (fig. 3), still longer than the correspond-
ing structure in that subspecies. The clasper of another
Mombasa specimen, which corresponds im appearance
with Grose Smith an Kirby’s P. gerda, is of the same
liliana character, but with a somewhat shorter spine (fig. 16).
The uncus of the first-named Mombasa specimen (fig. 17)
the charina Group of Pinacopteryx. 203
is long and slender, shaped like a surgeon’s curved bistoury.
That of the gerda-lke specimen (fig. 18) i is of similar charac-
ter, but slightly sharper at the tip. The scent-scale is of
the remarkable shape described on p. 196, and is charac-
terised by the presence of a dark granular patch at the
junction of the narrow portion of the lamina with its
expanded base (fig. 8, p).
(4) P. gerda, Grose Smith and Kirby.—The type described
and figured under this name,* from Mombasa, is probably
a dry-season male of P. liliana; but there is a form, as
a aT
~
Fig. 17.—P. liliana, Gr. Smith, Uncus x 54.
already mentioned, occurring at Voi, Mlegwa and Maranga
(all 1 in British East Africa), the male of which ; Is identical
in appearance with gerda as figured and described, and
to which the same name may perhaps be applied, at all
events provisionally. The upperside of the male in this
form appears to be always free from dark veining, and the
dark margin of the fore-wing is somewhat further prolonged
ae
Fiq. 18.—P. liliana, Gr. Smith. Uncus x 54.
towards the anal angle than in P. liliana 3. There is
usually an indication of a discocellular spot on the fore-
wing, but not on the hind-wing. Beneath, the general
surface of both wings may be white, as in a specimen from
Mlegwa (January) and one from Voi (May); or the hind-
wing and apex of fore-wing may be-yellow; pale, as in
another specimen from Voi (May), or deeper, as in two
from Voi (October). The discocellular spots are present
on both wings, but very fait on the hind-wing in both
* Rhop, Exot., Pinacopteryx, Pl, I, figs. 10, 11.
204 Dr. F. A. Dixey on
specimens captured in October. The large median spot
is always present, and there may be an indication of a
submarginal series on the hind-wing. The female is like
a wet-season or intermediate female of P. liana, though
usually smaller. It always possesses on both surfaces the
Fic. 19.—P. gerda, Gr. Sm. and Kirb. Spine of left clasper x 54.
spot between the median and submedian of the fore-wing,
as in those forms, and the discocellular spots on fore- and
hind-wing. The claspers in a male from Voi (figs. 19, 20)
are curiously unsymmetrical; the right valve ending pos-
teriorly in a sharp spine like that of liliana from Mombasa,
Fic. 20.—P. gerda, Gr. Sm. and Kirb. Spine of right clasper x 54.
and furnished, as in that form, with a terminal socket
from which protrudes a group of large chitinous bristles ;
the left valve also ends in a spine, but this, besides being
shorter and broader, is entirely destitute of a terminal
socket. The uncus of the same specimen (fig. 7), though
like that of P. liliana, is more deeply curved. It may be
the charina Group of Pinacopteryz. 205
called sickle-shaped. The scent-scales in two males from
the Voi River (fig. 9) and one from Mlegwa are of the
liana rather than of the simana type. The basal expan-
sion takes up more of the lamina and is more rounded
than in simana, but is much smaller and less rounded
than in lilana. Like the corresponding structure in
the latter form, the lamina shows a dark, granular,
circular or oval patch at the junction of neck with body
(fig. 9, p).
(5) P. venata, Butl.—This is the form which is found
in the White Nile region, Abyssinia (Lake Rudolph Expe-
dition), Southern Kordofan and the Southern Sadan at
least as far west as the Shari-Tchad Protectorate. It is
generally smaller than P. semana, and, especially in the
dry season, 1s sharper-winged in both sexes than that
insect. The upper surface of the male differs also from
that of P. simana in showing no dark veining; it may
possess in the wet season a few black scales in the situation
of the discocellular spot of the fore-wing, but is generally
destitute of all traces of these spots except a slight dis-
coloration showing through from beneath. ‘The fore-wing
possesses a dark apical patch passing into a hind-marginal
band; this patch and band in the dry season may become
pale and may almost disappear. There is also on the
hind-wing a row of marginal spots, often absent in the
dry season. Beneath, the male is white; in the wet season
the submarginal series is very often absent, but may be
indicated by a more or less complete chain of dark spots.
In the dry season the submarginal chain is usually better
developed; it is paler in colour, and on the hind-wing
frequently forms a festooned linear band. A slightly-
marked brownish irroration may be present on the hind-
wing and the apex of the fore-wing. There is generally
some dark veining on the apex of the fore-wing and outer
portion of the hind-wing at both wet and dry seasons.
The discocellular spots are always present; a marginal
row may also occur, especially in the wet season. On the
upper surface of the female the dark apical patch is broader
than in the male; as in that sex, it passes into a con-
tinuous hind-marginal band, darker and more pronounced.
in the wet season than in the dry. In the wet season the
dark veining of both wings is usually well marked, as in
Mr. Butler’s type; the hind-wing also carries a series of
large dark marginal spots. The submarginal chain of the
206 Dr. F. A. Dixey on
fore-wing ends in a large spot between the second and
third median branches ; there is no spot below the median,
such as occurs in P. liliana. A discocellular spot is present
on both wings in the wet season; in the dry season it 1s
often absent from the hind-wing, and sometimes from
both. Beneath, the hind-wing and apex of the fore-wing
are yellow, varying in degree “of intensity ; the remaining
area of the fore-wing is white, often with a yellowish shade
at the base. The veins of the hind-wing and of the apex
of the fore-wing are marked with dark lines, paler in the
dry season; at which period the same areas may also
show a slight reddish-brown irroration. Except in the
extreme dry-season form, a marginal row of spots is
generally to be found on the hind-wing. The submarginal
series of spots is usually present at both seasons, on the
hind-wing taking the form of a more or less continuous
festooned line; on the fore-wing it may be very slightly
developed, but always includes the characteristic spot
between the second and third median. As on the upper
surface, there is no spot posterior to the median. Dis-
cocellular spots appear to be always present on both
wings. It may be observed that the dry-season specimens
from the White Nile are sharper-winged than the generality
of examples from Kordofan, and are also more conspicuously
marked. It is especially noticeable in the latter assemblage
that all the markings of the female on both surfaces are
in the dry season of the same reddish-sandy tint. In the
wet season the corresponding markings are dark brown or
black. The clasper of a male from Gondokoro ends
posteriorly in a spine (fig. 5) which is much blunter than
that of P. charina, liliana or gerda, but is slightly less
blunt than that of a P. simana from Gazaland. The uncus
(fig. 15) is ike that of P. s¢mana, but is still more sharply
bent downwards at the tip. The scent-scale (fig. 12) is
somewhat variable; but on the average is shorter, and
broader in proportion than that of P. simana, which it
otherwise resembles.
P. simana and P. venata are no doubt closely related,
though typical specimens are easily distinguished. They
may “perhaps intergrade in Uganda.
The chief points of distinction between Pinacopteryx of
the charina group may be summarised in tabular form as
follows :—
207
the charina Group of Pinacopteryx.
UGPUS
| *poaano | uleyynog § ‘uRjopIoy uaa |
* 910-0 | Aydreys f4yaoyg | -yuntq ‘4209 | “yUOSqYy “quosqy | -Yynog ‘eruissAqy ‘OTIN O9TY | ‘Tang ‘vynuae *q
| | | | | |
| | | | . ye . | .
*poammo | a ~ (eolapy “oT ‘Iq) | Aqaryt pure
* 760-0 | Ajdaeys £ suorT ‘suOT *S UL QUOSoIg ‘qUOSqY | PASO “VourIe_, “IOATY LOA | WIFE esory ppsab * qT
| *poarno ‘5 pure © ul quosqy | | “yqTUg
* eTT-0 | Apystys § Suory ‘SuorT |= & ur quosorg ‘@uUIyUoselg | pooymMoqysteu pur esequoyy | osorg = ‘unypy —“F
| | | | “RpUuRoy—)
| ‘(esequioyy JO pooymoq
-ystou oy} gdooxo) vorypy |
“4 ur uo1yeo wey pue peajua) ys |
| ‘poamno =| “qunyq -IpUL qurIey | ‘eIsopoyy, = “vol W seq
* 960-0 Ajdaeys Sqa0yg | AoA fq10yg eB = Aporey ‘qUosolg | ., URIUIOX) 5, PUR oseNnsnqIo0g | ‘ydoy ‘vunuis “gy
}
*poarno |
Apyysys £ Sucy | EeAS UE — be :
“UU 980-0 AToVIOPOT ‘DUCT “qUOsq ‘quosqy | ‘purpnnz ‘TeyeN ‘Auojog ode pslog “wur.wpyd *q
| |
er Ee ‘radsvy ‘yodg (2) ? pats
etl teed senou tl | Jo ae | UeIpemqng = uoIyvUAA ye TOTO LASE. |
208 Dr. F. A. Dixey on Pinacopteryzx.
Before closing this paper, I should wish to say that I
am far from supposing that the statements and conclusions
therein contained are necessarily final. It is quite possible
that a more minute examination of existing specimens, or
an accession of fresh collections from the above and other
districts, might render necessary a modification of the
present results. I can only claim to have done my best
with the material at my command; this comprises the
series in the National Collection at the British Museum
and the Hope Collection at Oxford, the latter containing
the very valuable consignments from Capt. R. S. Wilson
(Southern Kordofan), Mr. W. 8. Loat and Dr. G. B. Long-
staff (White Nile), the Rev. K. St. A. Rogers (British Fast
Africa), Mr. C. A. Wiggins (Uganda), Dr. G. D. H. Carpenter
(“ German” East Africa), Mr. 8. A. Neave (Rhodesia),
Dr. Longstaff and Mr. G. A. K. Marshall (Cape Colony,
Natal, Gazaland and Mashonaland), with others. The care
taken by all these gentlemen to furnish their specimens
with exact and ample data as to locality and time
of capture calls for grateful recognition on the part of
those to whom belongs the task of working out and co-
ordinating the material provided by their several collec-
tions. It is impossible to overestimate the value, for
bionomic purposes, of accurate notes of this description.
To Dr. Eltrmgham I am indebted for the preparation
of a long series of genitalia, from which most of the outline
figures which accompany this paper have been drawn.
My special thanks are due to him for this and other help
which has always been most cordially given.
( 209 )
XI. Studies in Rhynchophora. IV. A preliminary note on
the male genttalia. By Davip Suarpe, M.A., F.R.S.
[Read June 5th, 1918. ]
Prats IX.
In its Transactions for 1912 the Entomological Society of
London published a paper by F. Muir and. myself on the
male genital tube of Coleoptera. That memoir was intended
to give an idea of the variety of structure of this part that
exists in the Order. It should evidently be followed by
a study of considerable extent of some one of the divisions
of Coleoptera, so as to gain a knowledge of the constancy
of the particular type of structure throughout that division.
In 1911 and 1912 Professor Niisslin contributed to the
Zeitschr. wiss. Insektenbiol. a paper entitled ‘* Phylogenie
und System der Borkenkifer,” in which he considers the
male genital structures of the European Scolytidae. It is
an excellent piece of work, but it is too limited to serve
the purpose of instructing us as to the constancy of type
of these structures in a “large Family of the Coleoptera.
The Scolytidae are a division of the Rhynchophora, and
Niisslin found the division to be highly polyphyletic; a
view which I believe to be correct.
Some three years ago I commenced a study of the genital
tube in Rhynchophora, but I have found it so long a task
that I think it desirable to publish a preliminary “‘hote on
the subject.
The Rhynchophora are probably the most extensive
natural group of species existing in the animal kingdom.
In the Munich Catalogue of Coleoptera 11,591 species of
the group are listed. This was in 1871, and since then the
number of described species has more than doubled. No
general catalogue of the group of later date has yet appeared,
but fragments have been dealt with in the Schenkling
publication. One of these, the Apioninae (Col. Cat.
Berlin, 1910), by H. Wagner, includes 1060 species, while
the Munich Catalogue had less than 400. The other
divisions of Rhynchophora show a similar increase, and yet
there are large numbers of undescribed species in collections
and fresh ones are constantly arriving, so that we may
TRANS. ENT. SOC. LOND. 1918.—PaRTS I, Il. (DEC.) P
210 Dr. David Sharp’s Studies in Rhynchophora.
conclude that 200,000 is a minimum number for the
existing species, of which about 25,000 are described.
Hence it is not a matter of surprise that I have not yet
been able to obtain a sufficient knowledge to enable me to
speak positively as to the objects of my work. Iam, in fact,
unable to demonstrate the value of the male structures
for taxonomic purpose, yet I have done enough to convince
myself that they are probably of great value.’ But I fear
the task I have undertaken is likely to prove too much
for me to accomplish, and I therefore publish this pre-
liminary note in the hope that it may help to remove
certain misconceptions that are prevalent, and may be of
use to other students.
The morphology of the male genital tube is really very
simple. It may be reduced to an elongate continuous
tube, which is made to appear shorter and more com-
plicated by a system of invaginations, in some respects
comparable to an old- fashioned telescope.
Certain of the parts have received names from previous
writers, and, as I shall have to refer to these, I will here
mention the more important, viz. :—
Lindeman, Vergleichend-anatomische Untersuchung
iiber das maenliche Begattuneselied der Bor-
kenkaefer. Bull. Soe. Imp. Moscow, vol. 49, 1875,
pp. 196-252, 5 pls.
2. Verhoeff, in Abdominal segmente und Copulations-
organe, etc. Deutsche ent. Zeitschr. 1893, p. 156,
pl. iv, figs. 126-140.
3. Verhoeff, Ueber das Abdomen der Scolytiden. Arch.
f. Naturgesch. 62, 1896, 1, pp. 110-144,.2 pls.
4. Hopkins, on the genus Pissodes. U.S. Dep. Agric.
Ent. Techn. Ser. 20, part 1, 1911.
5. Niisslin, as already referred to on the foregoing
page.
Nos. 1, 3 and 5 refer to Scolytidae, a very exceptional
and difficult group of Rhynchophora; while No. 2 is but
brief, and comparative with other Coleoptera, and, again,,
No. 4 relates only to one genus. Hence the information
as to the genitalia of the great division is very small.
In figs. | and 2 I give a scheme of the arrangement of
the tube in Rhynchophora. These two figures are purely
diagrammatic, and in some ways do not convey an accurate
Dr. David Sharp’s Studies in Rhynchophora. 211
idea : the membranous part that connects with the body
is not exserted naturally; thus the symmetry is never
so complete as they lead one to suppose, and it is also
greatly interfered with by the muscles, as well as by con-
strictions, folds and pleats, and the alternations of very
hard parts with delicate membranes. In some forms
(such as Cronus) the tube can, however, be extended into
a form comparatively more elongate than in fig. 2.
In these diagrams the hard (chitinised) parts are repre-
sented by thick lines, the thin lines being membrane.
The features shown by these diagrams are constantly
present in all Rhynchophora, except that the spiculum is
absent in one division of the Calandridae and in Platy-
pidae; and that in the group last named there are no true
median struts, the basal prolongations of the median lobe
being there projections with membrane between them.
THe ABDOMEN,
.
The genitaha in Coleoptera are withdrawn into the
abdomen and completely concealed. Although the abdo-
men is not morphologically a part of the venitalia, yet the
two are so intimately connected functionally that neither
can be comprehended fully without a knowledge of the
other. There are, indeed, some who consider that the
genitalia in whole or in great part are really modified parts
of the abdomen, and Verhoefi entitles his paper on the
genitalia of Scolylidae, a study of the comparative anatomy
of the abdomen.
In Rhynchophora the abdomen is greatly modified at the
base of the ventral aspect in coadaptation with the meta-
sternum and hind coxae. On inspection five ventral
plates are seen, and these in descriptions are called the
first (basal) and so on to the fifth. There is membrane
concealed at the point of junction with the sternum, and
also a hard more or less perpendicular part or phragma.
These parts (which are not visible except by taking off the
‘abdomen) are considered to represent the sternites of two
segments. This is rendered in the highest degree probable
by the fact that the corresponding dorsal portion of the
abdomen has seven plates in place of the five ventral ones.
In addition to the seven easily recognised segments
there is an eighth one, the dorsal part of which is usually
large, while its ventral plate is small; the ventral plate
212. Dr. David Sharp’s Studies in Rhynchophora.
is usually membranous in the middle so as to be two distinct
plates, but sometimes it is entire, and this is a character
of much taxonomic importance. This last ventral may be
called the eighth, or the true last ventral, so that in the
ordinary course of counting, we pass at once from five to
eight. The two missing sternites are, as explained above,
re ally to be found at the base. Lindeman did not recog-
nise this, and started the idea that one of these apparently
missing plates was to be found in the genital tube in the
form of the spiculum gastrale. If that view be adopted, we
have really nine abdominal sternites and only eight tergites.
One of the complications in counting the abdominal
segments is found in the case of the family Belidae, where
there are superficially visible only seven dorsal plates.
This, however, is due not to any real deficiency, but
arises from the eighth segment being of very peculiar
form, and telescoped into the segment preceding it.
In the Australian Belidae the concealed terminal seg-
ment can be easily pushed out, and is then found to be
of very extraordinary shape, the dorsal plate being bent
so as to have as great a surface on the ventral aspect as
on the dorsal, and thus there is the simulation of an addi-
tional sternite. In the North American Ithycerus (which
is only a subfamily of Belidae) the terminal segment: is
constructed as in Belus, but is exposed and not telescoped
into the preceding segment. In this case there were,
therefore, considered to be six (instead of the usual five)
externally visible ventral plates; the error was, however,
corrected by Dr. G. H. Horn many years ago (cf. Leconte,
“ Rhynch. of North America,” Dp: Ii).
The last dorsal is not of so great taxonomical import-
ance as the last ventral; but it is subject to considerable
modifications, one of which deceived Kolbe into describing
it as the aedeagus. This error has been pointed out and
corrected by V: erhoeff, It is one that may be easily made
in that particular case (Rhynchophorus), and it has unfor-
tunately been copied in Packard’s text-book; but it may
be mentioned as showing the necessity of examining the
tip of the abdomen when we are studying the genitalia.
THE SPICULUM GASTRALE.
Close together, at the tip of the abdomen, we find to
investigate the ventral and dorsal plates of the last seg-
ment, the termination of the alimentary canal, the junction
Dr. David Sharp’s Studies in Rhynchophora. 213
of the genital tube with the body wall, and a peculiar
structure the spiculum gastrale. All these have origin
from a membranous area at the tip of the abdomen, and
this small and irregularly shaped membrane must be
treated as common to all the structures. On severing this
membrane so as to free the genital tube from the other
parts, we expose the tegminal layer of the genital tube
(the Paramerenrohr of Nii sslin). As this is the commence-
ment of the genital tube it is well to remark that the pos-
terior part of the tube is functionally its anterior part, as
shown in fig. 2. This complication as to the orientation
renders it desirable to use the terms basal and apical
instead of anterior and posterior; basal being nearer to
the centre of the body than apical is.
The spiculum gastrale is at once seen ; it is the ‘‘ Stengel ”’
of Lindeman, the ‘‘fork’’ according to Hopkins, the
*“spiculum’” of Verhoeft and Niisslin. It is present 1n
the great majority of Rhynchophora, but is absent in some
of the Calandridae, especially in those of very large size,
and it is also wanting in Platypidae. It is a curved
or sinuate rod, connected at the apical area, mentioned
above, with the tube at or near the base of the latter
when extended; it is of variable size according to the
species, and extends basally, its sinuation adapting it to
some extent to keep close to the tube, its musculature
is great. At its apex it forms a sort of fork with widely
separated, short prongs; but there are various forms in
which this structure is peculiar (cf. Nawpactus and to a
less extent Hpisomus). This part is closely connected
with the true last ventral plate, and this connection appears
to be not always a simple one. This structure is much in
need of investigation, especially as some anatomists con-
sider the spiculum to be a modified ventral plate (the 9th).
At the other (or basal) extremity the spiculum is generally
somewhat expanded and more abruptly curved, and some-
times greatly so. The spiculum diverges from the teg-
minal layer, of which I consider it to be a part, just as the
strut of the tegmen is a part of the tegmen.
Tue TEcmMInNAL LAYER.
This part of the tube connects with the apex of the
abdomen. It does not reverse or extend when the organ
is functioning, but is held in place by its connections,
including the spiculum and the true last ventral, so that
214 Dr. David Sharp’s Studies in Rhynchophora.
it forms a tube through which the median lobe protrudes.
It includes basally the tegmen, but the apical part is
entirely membranous and transparent, and is usually
omitted in figures, though the tegmen itself is nearly
always represented. In the paper by Muir and myself
this membranous part is called the second connecting
membrane, but we now consider it better to call this mem-
branous area the first, and in the figures it is marked aml.
A very interesting feature is found in the Rhyncho-
phorid group of the Calandridae, inasmuch as this mem-
branous area is more or less strongly and completely
chitinised, thus becoming to some extent similar to the
“ body ” of the median lobe. In certain forms, referred
at present to the group Sphenophorides, the spiculum
proceeds from this chitinised part, and the structure then
appears to resemble the tegmen. This condition is figured
in the Transactions of the Society (1912, pl. 76, fig. 224a).*
This condition is instructive, as it shows that a part of
the tube that is usually membranous can become chitinised,
and that chitinisation is secondary to the membranous
condition; a fact that should not be lost sight of. The
term “connecting membranes ”’ is itself objectionable, as
it tends to convey the idea that they are of secondary
importance, and merely connect the hard parts, while
the fact is the integrity of the tube is the primary object
of the whole mechanism.
Proceeding basally along the tube we come to a
chitinous structure of a more or less transverse nature,
but differing greatly in the various forms of Rhyncho-
phora; sometimes it forms a simple ring, at others an
incomplete ring, but it is usually provided ventrally with
a single strut projecting basad. This hard part of the
circumference of the tegminal layer is the ‘‘ tegmen ’’ (Sharp
and Muir), the ‘‘ Gabel’ of Lindeman, Verhoeff and Niisslin.
It is of great taxonomic importance, especially in the
families of Rhynchophora that are separated from the
Curculiondae; the part that is dorsal taking on there a
great development (Anthribidae, Brenthidae, Rhynchitidae,
Microceridae, Brachyceridae, Belidae, A pronidae, Attela-
bidae), all of which have a large “ cap-piece,” differing in
form according to the family. In various forms of Cur-
culionidae there is no cap-piece, this being, of course, the
* In the explanation of the plate this part is said to be the tegmen,
which is an error: for “‘tegmen” read there “* pseudo-tegmen.”
Dr. David Sharp’s Studies in Rhynchophora. 215
case in the forms I have mentioned as having the teemen
in the shape of an incomplete ring.
Although I wish to avoid at present all pointy of
wltra-morphology, yet I think it is only proper to remark
that the functions of the tegmen as part of a mechanisin
are complex, and until they are ascertained—at any rate
to a certain extent—we must merely make use of the fact
of constancy or inconstancy, for taxonomical purposes.
Verhoefi (Arch. f. Naturges, 62) treats the ‘‘ Gabel” as
** Paramerenreste.”’
So much doubt exists as to the ultra-morphology of
‘ parameres ”’ in Coleoptera, that the term has been alto-
gether abandoned by Muir and myself. And this not
because the term is a bad one, but because of the great
amount of theory that is associated with it. As an in-
stance of this | may mention that Verhoeff in the memoir
cited states (p. 139) that “ the parameres of male Coleoptera
are the true genital appendages.” From what follows it
appears that he means by this that the median lobe is the
equivalent of a body segment, or somite, and that parameres
are the equivalents of appendages of a somite (7. e. of legs,
or of palpi). Such a view is almost or quite metaphysical,
and I hope that I may be doing an injustice to Verhoeft
in believing that is what he is promulgating.
In Rhynchophora the structure of the tegmen and the
condition of the membranous areas immediately adjoining
it are complex and varied, so that a special memoir on this
part will have to be prepared. I am not able to give any
information of a thorough nature on the matter, and in
some forms where the tegmen is complex (Brachycerus,
Microcerus, Anthribidae, and others) I anticipate that a
knowledge of the development will be essential, for there
appear in some cases to be folds that have become solidified
by chitinous exudation.
The tegmen is placed at a part of the tube where, accord-
ing to observations of F. Muir, a primary invagination
occurs in development. This of itself must give rise to
folding or doubling of the walls of the tube at this spot,
and this is probably the real starting-point of the tegminal
complications.
THe Meptan LOBE.
Near or at the tegmen there exists a turn down of the
membrane, which results in the connection of the mem-
216 Dr. David Sharp’s Studies in Rhynchophora.
brane with the body of the median lobe; this intervening
membrane has been called by Muir and myself first con-
necting membrane, but I here call it the second. This
lies within the teominal layer, and is, in fact, a continua-
tion turning apicad thereof. It may be called the median
lobe layer. This layer is mentioned by Niisslin, who calls
t ‘“ Penisrohr,” but he does not mention that it is con-
tinuous with the other layer, being an invagination thereof,
the tegmen being chitinised at or near the line of invagina-
tion. It must not be supposed that this point can be at
once settled by a slight examination; for the doubling
is usually complex, and accompanied by creases, as the
folding of the dorsal part of the circumference may not be
at the same transverse line as the ventral folding, and may
be accompanied by a tuck or overlap. Moreover, this part
of the tube is the subject of considerable variation in
leneth according to whether the tegmen is drawn back
or pushed forwards, or the median lobe extended; this
membrane is often very crumpled up. Our fig. 2 shows it in
an imaginary simple form, and it can in some forms, such
as Cionus, be actually extended into something like that.*
This intervening membranous area—im2—is_ really
common to the tecminal layer and to the median lobe
layer: in repose it is crumpled up under the protection of
the tegmen, but when the median lobe is extended as in
fig. 4 the crumpling disappears.
The median lobe is called by Lindeman the *‘ Kérper,”
by Hopkins the “stem,” by Verhoeff and Niisslin the
“penis.” It differs so much in form that it is difficult to
give a general description of it; for our present purpose
we may merely say that in some forms (Nauwpactus sul-
phurifer. Erythrapion, etc.) it is a long slender hard tube,
while in other cases it is more or less membranous along
the dorsal surface except at the sides, and this form, which
is very common, is shown in our fig. 3, and is well exhibited
by Hopkins’ plate xi of the “ stems ” of. Pissodes, though
his figures do not convey any indication of the fact that
this trough- like structure is really a tube, the sides of the
trough being connected by membrane.
Whatever the shape of the median lobe it always pos-
sesses in Rhynchophora basally a pair of projections which
* My daughter prepared for me a series of drawings to illustrate
the elongation of the tube in Cionus ; but as a whole plate would be re-
quired for it, publication must be deferred to a more fayourahle time,
Dr. David Sharp’s Studies in Rhynchophora. 217
we call the struts of the median lobe; Lindeman and
Niisshn call them “ Fiisschen,”’ Verhoefl and Hopkins
‘*femora’’ : in Latin diagnostic I eall them ‘‘ temones.”
These struts are present in all Rhynchophora;* and
though wonderfully constant in the same species, they
display much variety in the different forms. They are
certainly of considerable taxonomic importance. Some-
times they are so short (Lixidae) that they escape notice
if a short portion of em is left on the preparation. In
other cases they are very long (in Cycloterinus foveatus,
Kolbe, they extend far into the prothorax and are so
Blender that the aedeagus can only be extracted with great
care). The form of the struts is also very constant in the
same species. They are definitely elongations of the mem-
brane, tubular, and filled with chitin; in certain cases this
structure is evident; in some forms they appear to be dis-
connected from the body, but there 1s always a membranous
connection, though the chitin may be deficient for a brief
space. Such cases occur when the struts come off with a
ereat elbow from the lobe (cf. Szfones). The struts are some-
times quite short, and assume the form of callipers; but so
far as I know this is only the case in Lixidae.t The struts,
besides being areas for muscular insertion, seem to be, to
a certain extent, a protection to the invaginated sac when
this extends basally beyond the body of the lobe. When
the sac is elongate the struts are sure to be long. The
composition of “the body of the lobe shows important
distinctions that are, I have no doubt, of taxonomic im-
portance ; see as to this Calandridae, Brenthidae, Rhina, ete.
The median lobe does not enter into the genital tube
of the female, but only opens its terminal cloaca (not the
internal cavity called by Stein the cloaca). On the dorsal
surface of the median lobe, more or less close to the apex
of the lobe (sometimes at the apex, as in fig. 3), there
will be seen an area evidently different from the con-
tiguous parts: this is the place where the evagination of
ane sac occurs, and has been called the median Grice: but
is not an orifice, but only the spot where the sac is
invaginated, or, as the case may be, inverted.
* They are not present in Platypus; the projections there found
being of a different nature, as I have previously stated.
+ In Hopkins’ figures of Pzssodes the struts are depicted as
amalgamated at their termination: this is a mistake, nothing of
the sort occurs in any Rhynchophoron,
218 Dr. David Sharp’s Studies in Rhynchophora.
THE Sac.
The more intimate part of the copulatory mechanism is the
sac (called by some ‘‘ praeputial sac,’ though the name is
amisnomer). This structure is predominately membranous
though it has various chitinous bodies in its walls. This
is the structure that enters the genital tube of the female,
one of the functions of the median lobe being to bring this
male structure into such a position that it can enter the
female parts notwithstanding its membranous texture. It
is protean in form, and exhibits the most wonderful diver-
sities of shape. A comparatively simple form is shown in
fig. 4, a more voluminous and complex one in figs. 7 and 8.
In repose the sac is packed away inside the median lobe,
but most frequently the apex of the sac projects more or
less from the base of the median lobe, where it can be seen
with the duct entering it. The sac has a variety of struc-
tures in addition to its marvellous development of lobes;
these structures form the armature of spines and thorns,
as well as of minute papillae, etc. In addition to this
armature, there is an adjunct of the duct of an important
nature, placed in the wall of the sac where the duct enters.
In fact, this structure is the completion of the copulatory
mechanism. The duct enters it, and when the sac is
everted the apparatus is carried with it and becomes the
apical part of the sac; the functional orifice is seated on
this little mechanism, and it is at this spot that the sperm
leaves the male part of the genital conduit and becomes
the appurtenance of the female. I call this the transfer
apparatus. It differs greatly in various Rhynchophora.
Our fig. 5 shows it in Polycleis plumbeus (a South African
Otiorrhynchid), and fig. 6 exhibits it more highly magnified.
It is seen to consist of a median structure, into the base of
which the duct enters, terminating at its apex; the frame
part is subsidiary. A structure more or less like the
median portion of the apparatus (fig. 6) is very common,
and the form may be considered as a vase-like flagellum ;
sometimes by great elongation it becomes a slender or
whip-like flagelium, which may be several times as long as
the whole insect; but usually the flagellum is shorter than
this. I have examined this structure in a series of species
of the genus Holonychus, where it varies very greatly in
development, being in some larger than the flagellum of
Polycleis (fig. 6), while in other species it is minute and
difficult to detect. |
Dr. David Sharp’s Studies in Rhynchophora, — 219
As the sac is the part of the coleopterous genital tube
that has been hitherto least investigated, I shall venture
to say a little more about it than my knowledge really
justifies; for its study is much more difficult than that of
any other part, so that it has been too often passed over
entirely, or without a word as to its being the essential organ
of intromission, to which the other parts of the mechanism
are merely accessory. The membranous part of the sac—
its walls and lobes—and any chitinous armature borne
thereon must be considered as conveyers of the transfer
apparatus to the spot where it can be effective. The
functional orifice appears to be always minute even when
the other parts of the apparatus are voluminous. In the
case of the very long—whip-like—flagellum it is most
difficult to actually see the aperture, for the structure
cannot be set on end, but the long and slender apparatus
may be said to be as fine as it 1s possible for a chitinous
duct to be. Now, though there can be no doubt that in
many Rhynchophora the sac to be functional must be fully
extended, for the sessile—or even very minute (in Holony-
chus deflecus and H. gracilis, spp. n.) transfer—apparatus
is situate at its extremity, we may nevertheless doubt
whether in other cases anything more than a slight or
partial eversion occurs. From this point of view the
Otiorrhynchid forms assigned to the Celeuthetides are very
interesting, for in some of them the length and tenuity of
the sac render ‘: total eversion of the structure very im-
probable. Fig. 9 (Lrigonops, or Heteroglymma, sp. n.?,
New Guinea) uaa one of the longest and most slender
of these sacs; it contains a rather long curvate flagellum,
attached to the wall of the sac only at the base where it
is a little swollen and notched. It will be noticed that
there exists also in the interior of the body of the lobe
another structure which has all the appearance of being a
tube (fig. 9y) through which the slender flagellum may be
thrust and would then protrude sufficiently for intro-
mission. All that appears necessary in this case is for
the sac to be everted (or perhaps moved apically without
eversion) so that the flagellum passes into the director
and protrudes; possibly the director may then itself
move apically to a greater or less extent.
The transfer apparatus of the sac reaches its greatest
complexity in the Scolytidae. Hence it attracted the
attention of Lindeman, who called the whole of the pieces
220 Dr. David Sharp’s Studies in Rhynchophora.
“ Aufsatz,” while Niisslin prefers to call them the “ acces-
sory parts.” Attempts have been made to homologise
them, but sufficient is not known of their functions at
present. The part on which the functional orifice is
situate should be some guide, but this has hitherto been
too much neglected. As to the other “ accessory parts ”
little can be considered as settled. There are great differ-
ences in the inner structures of the tube in Scolytidae.
The subject has been discussed at length by both Verhoeff
and Niisslin in their considerations of Lindeman’s views.
IT can at present add nothing, though I may be permitted
to say that it is not clear that the sac functions in all the
groups in the same manner. As regards the variety in
the “‘acessory parts” of the Scolytidae reference may be
made to Lindeman’s plates, and to Niisslin’s discussion of
the point (Z. w. Insbiol., 1912, pp. 81-4). The necessity
of caution in homologising from simple inspection is evi-
dent from the fact that Niisslin considers the thirty-four
genera of Scolytidae found in Germany to belong to at
least twelve distinct subfamilies (loc. cit., p. 206).
Tue Duct.
This is another part that needs special investigation,
having been hitherto much neglected. It is sometimes
extremely long. Of course if a very long sac has to be
everted, there must be also a long duct, as this is carried
as far as the sac is extended. Usually the duct is very
easily seen, as it is surrounded by a very thick muscular
coating, but this disappears on maceration and the canal
is then fragile and difficult to detect. For the few par-
ticulars as to its course in Scolytidae refer to Niisshin (loc.
cut., p: 20).
Mertuops.
The means of making a rapid examination of these parts
are: have the insect to be dissected thoroughly penetrated
by water, keeping it at or near the boiling point for a minute
or two if small, for a quarter of an hour or more if large.
Take off the abdomen and place it in a strong solution of
eaustic potash, having previously opened the abdomen at
one side, so that the macerating fluid shall enter in
readily everywhere. Leave it in the potash for a time
varying, according to the size and delicacy of the specimen,
from a few minutes to seyeral hours. Take it out and put
Trans, Ent. Soc. Lond., 1918, Plate 1X.
SS
MALE GENITALIA OF RHYNCHOPHORA.
is fi
7
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1s ve hero hats i Po Wernne | al nt
7 ‘oe " <* ae Ft 7
Iyeral + wetted | bic SMsthorrli Sih eva This, ‘ AG
Sr Lae i) ivi iy ae) cert is At lh gag v/
DUNN Ar eee oN Pitas tubo Prireaiht i)
Os AL CATs ros ) aes
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ai!
yu
Dr. David Sharp’s Studies in Rhynchophora. 221
it in water, and wash away the macerated portions, and
when this is well completed attempt the eversion of the
sac. This is a delicate operation and requires experience
and patience to obtain success. Make a minute hook by
turning the point of a fine needle, and then blunt this so
that it will catch the wall of the sac and enable a pull to
be made on it without penetrating or tearing the sac. The
difficulty is to hold the specimen without compressing it ;
this is best done under water with the aid of a little cotton-
wool. Then tease the sac out little by little from the
median orifice, and when it is everted take a very finely
pointed pipette and inject it with the water. When it is
restored to its natural form, it should be placed under the
microscope and drawn with the camera lucida at once,
for there is no way known to me of fully preserving the
shape after mounting. In the case of small specimens
the chances of success are much reduced, and if the median
lobe is a long, slender, hard tube the sac cannot be arti-
ficially everted. It can be cut out by splitting the median
lobe, but this is of comparatively little service as it shows
only the wrong side of the sac. Any one who can invent
methods of overcoming the difficulties will be rendering a
ereat service to entomology. Specimens that have. been
killed and preserved in spirit are not suitable for examina-
tion of the sac, as it never regains pliability thoroughly.
The time occupied by maceration can be greatly reduced
by heating the fluid, but without caution and experience,
this is likely to result in spoiling the specimen.
I must not conclude without thanking Mr. and Mrs. F.
Muir for their assistance, as it is to them that the illustra-
tions are due.
Description oF Puate IX.
Lettering of all the figures :—
8 = eighth tergite or dorsal plate.
viii = eighth sternite or ventral plate = true last ventral.
an = orifice of alimentary canal.
cm (or im) = connecting or membranous area, between (1) tegmen
and apex of body, and (2) between tegmen and median lobe.
ec = external cloaca.
ej = duct proceeding from the testes (in fig. 4 the duct has dis-
appeared owing to reduction of the drawing).
222. Dr. David Sharp’s Studies in Rhynchophora.
fl = flagellum = transfer apparatus or a part thereof.
Jo = functional orifice.
im, see cm.
is = sac, usually concealed in median lobe.
ml = median lobe.
mo = orifice of median lobe = spot from which the sac is exserted.
ms. = struts of median lobe.
sp = spiculum gastrale.
fa = transfer apparatus or a part of such: see fl as above, and 2,
y, below.
tg = tegmen and
ts = tegminal strut.
# and y= parts of accessory apparatus, presumed to be portions of
transfer apparatus.
Fic. 1. Diagram of the arrangement of the genital tube in repose ;
see p. 210.
2. The same fully extended. The lettering is the same as in
the other figures.
3. Otiorrhynchus difficilis (from Piedmont), median lobe.
4. O. difficilis, sac extended and tegmen in situ: this is a fair
average of the Otiorrhynchid aedeagus, except that the sac
is longer than usual. '
Polycleis plumbeus (Pretoria), lateral view with sac imper-
fectly extended and duct still visible in it, tegmen cut away :
the pieces at the base of the sac assist in the eversion thereof,
and may correspond to the “* Endplatten ’’ (Lindeman).
6. Polycleis plumbeus (another specimen, from Cape Good Hope),
ot
transfer apparatus.
7. Isomerinthus, sp. n. (Amboina, F. Muir). Profile : enormous
development of sac, which can scarcely be compressed into
the median lobe which is enlarged towards the apex; tegmen
taken off.
8. Another specimen of the same species (Amboina, F. Muir)
with the sac partially everted, and injected.
9. Trigonops (? Heteroglymma), sp. (New Guinea). Another
Otiorrhynchid allied to fig. 8, but sac not extended and
probably very different, the median lobe being differently
shaped, probably conformably with the difference in the
sacs: x and y are seen through the wall of the median lobe,
and one or both are probably accessory parts of the transfer
apparatus, which is in this species very slender at the tip, an
intermediate between a “ whip-flagellum ”’ and a sessile
transfer apparatus (shown in fig. 6).
XII. Notes on the Ontogeny and Morphology of the male
genital tube in Coleoptera. By FReprERiIck Murr, F.K.S
_ [Read June 5th, 1918 ]
PrATE: XxX;
In a former paper* I described some stages in the develop-
ment of the male genitalia of some species of Coleoptera
Since then I have filled in a few more stages of the same
species, but I have not been able to extend my observations
to other forms. I would not consider it of any use to repeat
what I have said elsewhere were it not that some of the
leading authorities on insect morphology have failed to
understand the structure of the organ, and most workers
repeat their statements without any qualifications. Kolbe +
in describing the male genitalia of Rhynchophorus phoenicis
has mistaken the eighth ¢ abdominal segment for the aedeagus,
and the rectum for the ejaculatory duct. Several writers
have stated that the median lobe and the tegmen are com-
posed of amalgamated paired lobes or parameres, and
others have stated that certain segments, or parts of seg-
ments, of the abdomen are included in the structure. As
an extreme exponent of this latter view I may quote
Hopkins,{ who has tried to homologise the armature on
the internal sac with parts of the tenth abdominal segment.
I can find no evidence to support these views either in
development or comparative morphology.
DEVELOPMENT
In the early stages of Rhabdocnemis obscura (Boisd.) the
testes are connected by a Y-shape thread to a median
point between the ninth and tenth abdominal sternites.
During the development of the pupa the area where the
thread is attached to the body wall invaginates and forms
the genital invagination. The bottom of this invagination
- Psyche 2 22 (1915), pp. 147-152, pl. XIT.
+ ‘“ Einfiihrung in die Kenntnis der Insekten,” 1893, p- 322, figs.
225, 226, 227.
t “On the genus Pissodes,” U. 8S. Dep. Agric. Ent. Tech. Ser.
20, I, 1911.
TRANS. ENT. SOC. LOND. 1918.—PARTS I, II. (DEC.)
224 Mr. F. Muiz’s Notes on the Ontogeny and Morphology
grows out or evaginates, and eventually forms the eurazygos,
the stenazygos being formed by an invagination at the
apex of the eurazygos. The first differentiation of the
eurazygos is a constriction near the base, differentiating
the tegmen from the median lobe. This I call the tegminal
fold, and it is of great morphological importance ; from it
are developed the tegminal lobes as two evaginations, ard
the tegminal strut as a single invagination. ‘In R. obscura
(Boisd.) there are no tegminal lobes, but there is a large
strut, the origin of which as an invagination eventually
becoming thickly chitinised is quite plain. The portion of
the eurazygos distad of the tegminal fold develops into
the median lobe and the internal sac; at first there is no
differentiation between these two, but at a later stage the
basal portion becomes chitinised and differentiated as the
median lobe, while the distal portion remains membranous
and as it increases in size it crumples up and ultimately
it is withdrawn into the median lobe, but not until the
beetle is fully developed and has left the pupal skin. In
R. obscura (Boisd.) there is a pseudo-tegmen formed by the
chitinisation of the connecting membrane between the
tegmen and the wall of the abdomen, and in this species
the spiculum gastrale arises as an invagination from the
pseudo-tegmen.
The male genitalia of Coccinella repanda arise in a similar
manner from the same position between the ninth and tenth
sternites. Soon after the tegminal fold is developed two
broad, flat processes grow out from it, and a small invagina-
tion takes place on the opposite aspect of the fold; the
former are the tegminal lobes and the latter is the tegminal
strut. The tegminal fold beneath (or at the base of) the
tegminal lobes grows outward carrying the tegminal lobes
with it, and eventually forms the median “ cap-piece.”
The median lobe elongates and muscles connect its base
with the tegminal strut, and as it lengthens and grows
inward it becomes curved. The spiculum is formed by an
invagination near the base of the ninth sternite.
Can ‘pophilus humeralis also follows a similar line of
development, the tegminal lobes first appearing as broad,
rounded outgrowths of the tegminal fold, the tegminal
strut being very small. The apical portion of the eurazy gos
is invaginated at an early stage and grows inward to a creat
length, an evagination takes place ‘at the junction of the
eurazygos and stenazygos which lengthens into the fine,
of the male genital tube in Coleoptera. 225
long flagellum. At a later stage the median lobe is differ-
entiated, but the basal portion of the internal sac is not
withdrawn into the short median lobe until the insect is
mature, The median strut arises as an invagination at the
base of the median lobe. At first both fhe median and
tegminal struts are simple, tubular invaginations, but
x a later stage the former becomes dilated at the apex, and
the latter broad and thin.
COMPARATIVE MoRPHOLOGY.
If we examine the abdomen of a generalised trilohe
coleopteron nine or even ten tergites and nine sternites
can be easily discerned (in Enarsus bakewelli there is a
distinct tenth sternite lying between the anus and the
aedeagus). In the Dermestid figured * there are nine
complete abdominal segments, the anus opening on a small
membranous tube below the ninth tergite, the aedeagus
lying between the anus and the ninth sternite. The ninth
segment forms a complete ring, and is prolonged into the
abdomen as a strut on the ventral aspect. In Rhyncho-
phorus ferrugineus only eight abdominal segments can be
traced; the eighth tergite is large, boatshaped, deeply
cleft at the base and slightly so at the apex, with the eighth
spiracle on the pleural area; the eighth sternite is small and
lies across the ventral aspect of the eighth tergite, and
together they form a tube through which the aedeagus
plays: the anus lies beneath the eighth tergite, between the
eighth tergite and the aedeagus. “The cloaca so formed is
closed by the meeting of the posterior edges of the seventh
tergite and seventh sternite. In Rhabdocnemis obscura
(Boisd.) a similar condition prevails. In both these forms
the connecting membrane is chitinised and forms a pseudo-
tegmen; in ”Rhynchophor us there is no spiculum. In
Acantholophus and Ithycerus the cloaca is closed by the
meeting together of the posterior edges of the eighth tergite
and seventh sternite, the eighth “sternite is small and,
together with the eighth tergite, forms a tube through which
the aedeagus plays. In the former there is a large spiculum
arising some distance from the base of the connecting
membrane, in the latter there is a distinct spiculum and
also a strut from the basal edge of the eighth sternite; the
* This is a common species in Honolulu, but I have no name for
it at present, and no specimens in England.
TRANS. ENT. SOO. LOND. 1918,— PARTS I, I. (DEC.) Q
226 Mr. F. Muir’s Notes on the Ontogeny and Morphology
eighth spiracle is plainly discernible in both these genera.
In ylesinus crenatus there is no chitinised eighth sternite,
and the spiculum is highly developed and serves in the place
of the sternite as part of the tube through which the
aedeagus plays. In some allied forms the eighth sternite
is represented i in various states of dechitinisation (or degener-
ation). The anal opening in these forms is situated on the
membrane between the eighth tergite and the aedeagus
(on the dorso-basal portion of the connecting membrane).
CONCLUSIONS.
The evidence derived from observations on the develop-
ment of the male genital tube in Coleoptera indicates that
it is a tubular organ arising in a median position from the
connecting membrane between the ninth and tenth sternites.
There is no evidence whatever to indicate that it is composed
of amalgamated paired organs (called parameres by some
authors). The tegminal lobes, cap-piece and tegminal
strut are secondary outgrowths from the tegminal fold.
The comparative @ study of the morphology. does not indi-
cate that any abdominal segment or sternite is incorporated
into the tube. In certain forms we find that ten tergites
and ten sternites are actually present, or ten tergites “and
nine sternites, and the aedeagus consists of complete tegmen
with tegminal lobes and basal piece and complete median
lobe; in other forms some of the segments or parts of seg-
ments are dechitinised and withdrawn into the cloaca, but
the aedeagus in these forms only contains the same parts as
do those forms in which the segments are chitinised and there-
fore demonstrable. It is therefore illogical to consider the
missing segments as incorporated into the genital tube.
In fact the evidence points the other way, as in those forms
in which the abdominal segments are reduced there is
generally a great reduction in the tegmen. As the spiculum
is an invaginated secondary tube which becomes highly
chitinised it is difficult to understand how it can represent
a sternite, and the most we can say is that it arises from,
or near to the position of the ninth sternite, in the same
manner as the false spiculum, or strut, mn Jthycerus and
Belus arises from the edge of the eighth sternite. Apodemes
similar to the spiculum in origin (invaginations of the
ectoderm) arise in various parts of the body in insects and
do not represent a sternite or a tergite, and occur in positions
of the male genital tube in Coleoptera. 92'F
g j|
where the surface of the body wall does not allow a large
enough surface for the attachment of muscles. In Rhab-
docnemis obscura (Boisd.) the spiculum arises from the side
of the pseudo-tegmen some distance from the opening of
the cloaca, and, as already stated, in Rhynchophorus there
is no spiculum. In Platypus also the spiculum is absent.
It is probable that the spicula in different groups are not
homologous.
The theory of the origin of the genital tube by the
amalgamation of paired organs finds its chief support in
the analogy drawn from such forms as the Dermaptera. In
that order there is a Y-shaped organ consisting of a single
basal piece with a pair of parameres. In one group
(Protodermaptera) there are two penes, one arising from
each paramere; in another group (Kudermaptera) there is
only a single median penis. This latter form is similar in
construction to the trilobe form of Coleoptera. I can find
no evidence to show that the single basal portion of the
organ is formed by the amalgamation of two parameres,
and it is quite possible, and even probable, that the para-
meres are secondary developments, the same as the tegminal
lobes in Coleoptera. The formation of the single median
penis of the Eudermaptera is not by the amalgamation of
the two, but by the suppression of one penis and the increased
growth of the other. Thus the analogy from Dermaptera
gives no support to the theory of the paired origin of the
tegmen, and refutes the theory of such an origin of the
median lobe.
It may be thought (though there is no evidence to indi-
cate it, and it is very improbable) that Coleoptera had paired
genital openings, or that Protocoleoptera possessed them.
The time when the ancestors of the order could have been in
that condition is so remote that it can have no bearing upon
the question. It is probable that the immediate preceding
stage to the Coleoptera or Protocoleoptera was such as is
found to-day in Zoraptera Silvestri, where there is a single
duct opening in a median position, a portion of which is
most probably protruded during copulation. It is the
telescoping and chitinisation of this eversible portion of
the duct that has constituted the organ as we now know it.
In the Anoplura and Mallophaga we have an arrangement
of parts in the male genitalia similar to those in the trilobe
forms of Coleoptera, with similar lines of development in
both groups. That these are cases of parallel development
228 Mr. F. Muir’s Notes on the Ontogeny and Morphology
and have no phylogenetic significance no entomologist of
any standing will deny.
Whilst recognising the great interest and value of much
of the work in comparative morphology of'recent years, I
cannot help entering a protest against the methods of
some of the workers who have made a fetish of homology.
Having selected what they consider to be a generalised form
they proceed to delineate and name each sclerite, and then
set themselves to discover similar sclerites in other more
specialised types. It is under the influence of this idea that
certain workers profess to find portions of the tenth
tergite and sternite in the armature and chitinisations on
the internal sac. If they would remember that an insect
is a double membranous tube with a number of invagina-
tions and evaginations, certain areas of which become more
or less stiffened by the deposition of chitin, and that the
male genitalia of Coleoptera i is a tubular evagination arising
from a median position between the ninth and tenth
abdominal sternites, they might recognise the improbability,
or even the impossibility, of a tergite or portion of a tergite
becoming attached to the apex of a tubular organ in such
a situation.
My thanks are due to Dr. David Sharp for much interest-
ing information, and for placing at my disposal his large
collection of dissections made since we ‘published our joint
paper on this subject in 1912.
EXPLANATION OF PLATE X.
FIGURES.
No. 1. Rhabdocnemis obscura (Boisd.).—Early stage of male genitalia
in the pupa. Cm, wall of the genital invagination; 1/,
tegminal fold; ml +- is, median lobe and internal sac;
jo, the functional orifice will eventually open here;
ej, ejaculatory duct; m, embryonic muscles between the
eurazygos and the stenazygos.
2. The same about half developed.
No. 3. The same fully developed or nearly so.
4. Coccinella repanda.—Karly stage of male genitalia in the
pupa.
No. 5. The same three-fourths developed.
No. 6. Carpophilus humeralis.—Early stage of male genitalia in
the pupa.
No. 7. The same nearly fully developed.
o. 8. Dermestis, sp., showing the nine abdominal segments and
N the aedeagus.
Trans. Ent. Soc. Lond., 1918, Plate X.
Free.
y Cm
mill 4
Li EY 8 wm EX hy |
DEVELOPMENT OF MALE GENITALIA. COLEOPTERA.
ae ah as hieg soi”
“une aa wa! :
ony vintith: he war: eetisOla te 5
‘s :
5 tr sites
; = Sinllivdail Joccnt denn ;
* ipenentie tivey come «it ag tipninitea sniotasg ith
South teAlpary astd aire iby Ted AA, PUI CHAE Siakigort,! 5: :
i Btoy Welaiedi ye ricaty Wh. elegy obs Rev eee Ry a et Be ‘ean
~ “ava dyin the ea
1 Re
Ca BTAR OLY le Pea
oi fcy SHO RNS =i
tu lead Hiitbaglt Je
Site ec) ales
tented a ieat ge 4
7 : ana ify «
: r a i i if
< _ ae
4
—
it
»
of the male genital tube in Coleoptera. 229
g 7}
LETTERING.
a, broken edge of connecting membrane.
an, anus.
b, armature at base of flagellum.
cm 1, membrane connecting the tegmen with abdomen.
cm 2, membrane connecting the tegmen with the median lobe.
cp, cap-piece, or median extension of the edge of the tegminal fold.
ej, ejaculatory duct.
jl, flagellum.
Jo, functional orifice.
is, internal sac.
ml, median lobe.
ms, median strut.
pstg, pseudo-tegmen.
sp, spiculum.
t/, tegminal fold.
tg, tegmen.
ts, tegminal strut.
DECEMBER 31, 1918.
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CONTENTS “OF “PARTS 7; IF
PAGE
I. Coleoptera of the families Ostomidae, Monotomidae, Colydiidae and
Notiophyyidae from the Seychelles and Aldabra Islands. By the late
ANTOINE GROUVELLE. Communicated by Hucu Scort, M.A., F.L.S. 1
II. New species of Staphylinidae from Singapore. Part I. By Matcorm
CaMERON, M.B., R.N., F.E.S. ete Seca ae eae Sats wae 58
UI. Australian Sraconidae in the British Museum. By Row1anp E. TuRNER,
1eyAishy Lae HSis coc sts ses =a 0 hac cee ms 06 91
IV. On the naming of Local Races, Subspecies, Aberrations, Seasonal Forms,
etc. By Lorp RoruscuILp, F.R.S., etc. ... a a6 nae sre LES
V. Molippa simillina, D.-Jones: A Correction. By E. DuKINFIELD-JONES,
VI. On Mimicry in certain Butterflies of New Guinea. By F. A. Drxey,
MeAL ED vEERIS i css tes es sce ae aR “0 ae £18
VII, An Instance of Mutation: Coccus viridis, Green, a Mutant from Pulvinaria
psidii, Maskell. By K. Kunut Kannan, M.A., F.ESS. ... ay «- 130
VIII. Some Remarks on Mr. Kunhi Kannan’s Paper, ‘‘ An Instance of Mutation.”
By E. Ernest GREEN, F.Z.S. Be 580 eee eee ao et) lag
IX. Observations on the Lepidopterous Family Cossidae and on the Classi-
fication of the Lepidoptera. By A. Jerreris TURNER, M.D.,F.E:S.... 155
X. The charina Group of Pinacopteryr. By F. A. Drxry, M.A.,M.D.,F.RS.,
Subwarden of Wadham College, Oxford... a0 so aes tae LOE
XI. Studies in Rhynchophora. IV. A preliminary note on the male genitalia.
By Davip Snare, M.A., F.R.S. os o06 bec 2c Ses fee 209)
XII. Notes on the Ontogeny and Morphology of the male genital tube in
Coleoptera. By Freprrick Muir, F.E.S. ... ane ee * se ao
Proceedings ... aoe aA aoe ook are i-xxxii
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47
XIII. New species of Staphylinidae from Singapore. Part
II. By Matcotm Cameron, M.B., R.N., F.ES.
(Continued from p. 90.)
[Read June 5th, 1918.]
Tue Groups Megarthropsini (n.), Tachyporini, Adinopsini
(n.), Gymnusini, Myllaenini, Pronomaeini and Diglottini are
enumerated in this second instalment of my paper. The
types are contained in my own collection.
MEGARTHROPSINI, n. group.
MEGARTHROPSIS, 1. gen.
Remarkable by the build of the head and thorax resembling to
a considerable extent that of the genus Megarthrus, but in the struc-
ture of the prosternum, coxae and the sexual characters “appears
undoubtedly to be closely related to the Tachyporini. e
Head ‘subtriangular, produced, narrowed, and rounded in front
of the eyes, limited by a fine raised line; eyes large and prominent;
temples represented by a small obtuse angle. Labrum transverse,
broadly emarginate, setose. Mandibles rather stout, simple, sharply
pointed at the apex. Maxillary palpi elongate, the Ist joint small,
the 2nd elongate, the 5rd half the length of the 2nd, the 4th longer
than the 3rd, fusiform. Mentum (pars antica) transverse, corneous,
quadrilateral, the anterior margin narrower than the posterior.
Labium transverse, partly corneous, broadly emarginate anteriorly ;
tongue broad, membranous, obtusely emarginate in front. Labial
palpi short, the 2nd joint shorter than the Ist and 3rd, the latter
truncate. Paraglossae strongly pectinate, not extending beyond the
tongue. Inner and outer lobes of the maxilla densely ciliated at
the apex, the outer lobe also ciliated along the outer border. Thorax
with the side-margins broadly explanate; prosternal process short
and pointed; anterior coxal cavities widely open behind, the episterna
not nearly meeting, the epimera wanting; mesosternum finely
grooved between the middle coxae which, like the rest, are approxi-
mate. Elytra scarcely extending beyond the metasternum, the dorsal
surface separated from the epipleura by a raised line, the latter com-
plete, and with a raised line parallel and close to the inner border.
Winged. Abdomen pointed, the sides narrowly bordered, the first
TRANS. ENT. SOC. LOND. 1919.—PARTS III, IV. (MAR.) RB
Sanian Dept
23, Dr. Malcolm Cameron on
ventral segment keeled. Legs moderate; tarsi short, 5-jointed,
the anterior pair with the first three joints shortly triangular, the
Ist of them considerably broader than those following, the 3rd
narrower than the 2nd, the 4th small, semicircular, the 5th elongate,
as long as the three preceding joints together; middle tarsi with the
first two joints broader than those following, the Ist longer than the
2nd, the 3rd and 4th smaller, about as long as broad, the 5th as long
as the three preceding together; posterior tarsi with the Ist joint
a little longer and stouter than the 2nd, the 2nd and 3rd subequal
a little longer than broad, the 4th as long as broad, the 5th as long
as the preceding three together. All the claws simple; tibiae feebly
setose. Appears to be related to the Trichophyini and Tachyporini.
45, Megarthropsis decorata, n. sp.
Elongate, fusiform, moderately shining, black, the sides and pos-
terior half of the thorax, abdomen and legs reddish-testaceous.
Antennae long, slender obscure testaceous, the middle joints infuscate.
Length 4 mm.
Head black, transverse, subtriangular, produced in front, gradually
narrowed, and rounded, and finely bordered; eyes large and promin-
ent; temples very small, forming an obtuse tooth; coarsely and
rugosely punctured, the front smooth and shining. Antennae long,
slender reaching the posterior margin of the elytra, the Ist joint
cylindrical as long as the 3rd, the 2nd much shorter, 3rd and 4th
joints subequal, 5th, 6th and 7th subequal, each a little shorter
than the 4th; 8th, 9th and 10th slightly decreasing in length, much
longer than broad, 11th elongate, pointed, as long as the 10th.
Thorax strongly transverse, broader than the elytra, widest at the
middle, from thence equally narrowed and strongly rounded in
front and behind, slightly emarginate behind the anterior angles,
which are rounded and produced, minutely notched in front of
the posterior angles, which are rectangular; anterior border broadly
emarginate, the sides broadly explanate; sculpture coarse and
rugose. Scutellum reddish-testaceous, coarsely punctured. Elytra
more than half as long again as the thorax, square, coarsely and
closely punctured, the sides with very short, stout setae. Abdomen
elongate, pointed, reddish-testaceous, the 4th and 5th (visible)
segments a little infuscate, finely, indistinctly and moderately
closely punctured, ground-sculpture indistinct, coriaceous; lateral
setae wanting.
3. Eighth dorsal segment divided by three narrow triangular
excisions into four pointed, triangular processes, of which the central
pair are a little longer than the lateral, these latter furnished at the
New Species of Staphylinidae from Singapore. 233
apex with a very long seta, the central pair with a short seta at the
apex; eighth ventral segment divided by a flask-shaped excision
into two pointed lobes the apex of each furnished with a long seta,
the side-margins of the segment with a small tooth bearing a long
seta; seventh ventral segment with broad emargination limited by
a seta on either side at the posterior margin, the surface in front
with a triangular impression (the base corresponding to the emargina-
tion) extending the whole length of the segment, the posterior part
of which is studded with minute granules. Sixth and fifth segments
impressed in the middle line.
2. Eighth dorsal segment cut into four pointed processes, the
lateral being a little longer than the median pair, and each with a
long seta at the apex and a small tooth on the external margin also
carrying a long seta; central processes each with a short seta; the
lateral excisions deeper and narrower than the median one; eighth
ventral segment with six processes, the lateral much shorter than the
rest which are of equal length, the central pair broader and rounded
at the apex and furnished with a bunch of short yellow setae, the
others each with a long seta; the three central excisions are moder-
ately broad and rounded at the apex of each.
Hab. Mandai, in wet rotting leaves on the edge of a
jungle stream. Three examples.
TACHYPORINI.
46. Conosoma robustum, n. sp.
Xobust, convex, black, moderately shining; the abdomen rather
densely clothed with short golden pubescence. Antennae long and
slender, the first four joints and the last testaceous. Legs reddish
testaceous, the outer margin of the anterior tibiae closely set with
short black pectinations. Length 5mm. (in well-extended examples).
Build of C. bipustulatum, Gray., but more robust, broader, and
more convex. Head very finely and sparingly punctured, with scanty
cinereous pubescence,. and without ground-sculpture. Antennae
slender, reaching a little beyond the posterior angles of the thorax,
the Ist and 3rd joints elongate, of equal length, the 2nd half the
length of the 3rd, the 3rd and 4th subequal, the 5th to 10th each
longer than broad, subequal and compressed, 11th elongate, oval,
longer than the 10th. Thorax broader than the elytra, scarcely
transverse, the posterior angles rounded, the posterior margin
narrowly and obscurely ferruginous; very finely and rather closely
punctured, and covered with a short fine griseous pubescence.
Elytra as long as the thorax, slightly narrowed behind, with punctur-
234 Dr. Malcolm Cameron on
ation and pubescence much as on the thorax; ground-sculpture
very fine, transversely strigose; the sides without setae. Abdomen
pointed, the posterior margins of the segments narrowly and ob-
scurely reddish; puncturation very fine and rather close, pubescence
fine, golden; sides and apex with long black setae.
3. Eighth dorsal segment divided by a deep excision into two
lobes, furnished with long black setae.
®. Eighth dorsal segment divided into four blunt lobes, of which
the central pair are a little longer than the lateral and the median
triangular excision not so deep as the lateral ones.
Hab. Woodlands, in old logs.
47. Conosoma rufobrunneum, n. sp.
Reddish brown, rather shining, elytra darker, posterior margins of
the anterior and the whole of the last two abdominal segments clear
reddish-testaceous. Antennae scarcely extending beyond the pos-
terior angles of the thorax, slightly thickened towards the apex,
testaceous, the middle joints a little infuscate. Legs reddish-
testaceous. Length 3 mm.
Build of C. breve Fauv., but smaller and differently coloured.
Head dark reddish brown exceedingly finely and rather sparingly
punctured; pubescence fine and golden. Antennae with all the
joints longer than broad, the 2nd shorter than the 3rd, 4th to the
10th laterally compressed, gradually decreasing in length, 11th
elongate, twice the length of the 10th. Thorax but slightly broader
than the elytra, not so dark as the head, very finely and moderately
closely punctured ; pubescence fine and golden. _Elytra more or less
infuscate on the disc, rather more closely punctured and pubescent
than the thorax, slightly shorter. Abdomen very finely punctured
throughout, pubescence golden (owing to the colour of the abdomen
and the golden pubescence it appears in certain light to have a red-
gold iridescence); lateral and apical setae strong, black.
Hab. Mandai, in decaying logs.
48. Conosoma flavogattatum, n. sp.
Pitchy-brown, the posterior angles of the thorax, a round spot at
the base of each elytron, the posterior margins of the abdominal
segments (except the last), the first four and the last joints of the
antennae and the legs, testaceous yellow. Length 3°5 mm.
In build somewhat resembling C.fusculum, Er., but a little longer
and broader. Head exceedingly finely and very sparingly punc-
tured; pubescence yellow, fine, and sparing. Antennae extending
New Species of Staphylinidae from Singapore. 235
a little beyond the posterior angles of the throax, all the joints
longer than broad, the penultimate compressed laterally, the 2nd
joint shorter than the 3rd, the 3rd and 4th of equal length, the 5th
to the 10th gradually decreasing in length, the 11th long oval, longer
than the LOth. Thorax pitchy-brown, the posterior angles testaceous
yellow, very finely and moderately closely punctured; pubescence
fine, griseous. Elytra a little shorter than the thorax, pitchy-brown,
with a large round yellow spot at the middle of the base of each;
puncturation similar to that of the thorax, the pubescence golden
yellow on the spots, otherwise griseous. Abdomen pitchy-brown,
shining; the posterior margins of the segments testaceous, except
the last which is pitchy; puncturation and pubescence very fine and
close; lateral and apical setae black; eighth dorsal segment divided
into four long triangular processes by three triangular excisions.
Hab. Bukit Timah, in rotten logs. Two specimens.
49. Conosoma abdominale, n. sp.
Black, shining, the abdomen ferruginous red; the first four joints
of the antennae and the apical half of the last and the legs, testaceous
yellow. Length 2°8 mm.
A shining, sparingly pubescent species, somewhat resembling in
build C. immaculatum, Steph., but much more shining, blacker, rather
broader and more convex, and with much longer antennae. Head
black, shining, with a few scarcely visible punctures, almost glabrous.
Antennae extending a little beyond the posterior angles of the thorax,
the 2nd, 3rd and 4th joints elongate, subequal, the 5th to the 10th
compressed, the first of them a little longer than broad, the rest sub-
equal, scarcely longer than broad, the 11th oval oblong, nearly as
long as the two preceding together. Thorax black and shining, the
posterior margin narrowly ferruginous (by transparency); punctura-
tion very fine and not close, and in addition there are a very few
larger, superficial punctures visible; pubescence sparing, griseous,
very short and fine. Elytra transverse, as long as the thorax; punc-
turation and pubescence as on the latter, and with a few larger
superficial punctures of irregular distribution; ground-sculpture
fine and imbricate ; sides without long setae. Abdomen ferruginous,
the anterior segments with similar puncturation, ground-sculpture
and pubescence to that of the elytra, the posterior segments much less
distinctly punctured; sides and apex with long black setae; eighth
dorsal segment with a deep, nearly parallel-sided excision.
Hab, Mandai, in débris. One specimen.
236 Dr. Maleolm Cameron on
50. Conosoma championi, n. sp.
Black, moderately shining, the posterior border of the thorax, the
elytra near the suture and the posterior margins of the first three
abdominal segments more or less obscurely reddish. Antennae long
and slender, much longer than the head and thorax, the first four
joints and the last testaceous, the rest infuscate. Legs reddish-
testaceous. Length 3°5 mm.
Stature of C. binotatum, Grav., but the elytra much shorter. Head
very finely and sparingly punctured and pubescent. Antennae
long and slender, extending beyond the posterior angles of the thorax,
all the joints considerably longer than broad, the 2nd half the length
of the 3rd, the 3rd to the 5th subequal, the 6th to the 10th very
gradually decreasing in length, the 11th long, oval, longer than the
10th. Thorax very finely and moderately closely punctured, pubes-
cence short, greyish; the posterior border obscurely and indetermin-
ately reddish. Elytra transverse, scarcely longer than the thorax,
obscurely reddish about the suture and the posterior margins, the
puncturation as on the thorax, but a little more distinct; the
pubescence as on the thorax; sides without setae. Abdomen
with the posterior margins of the first three segments more or less
reddish; puncturation very fine and close in front, more sparing
posteriorly ; sides with long black setae.
Q. Eighth dorsal segment cut into four pointed processes by three
excisions, the lateral ones a little deeper than the central; the
processes furnished with long black setae.
Hab. Bukit Timah.
51. Conosoma walkeri, n. sp.
Black moderately shining, the posterior angles of the thorax,
the posterior third of the elytra obscurely, and the posterior margins
of the abdominal segments rufo-testaceous. Antennae not much
longer than the head and thorax, the first four joints and the last
yellow testaceous, the rest infuscate. Legs reddish-testaceous.
Length 3 mm.
In build and colour so similar to the preceding, that it will be
sufficient to give the differential characters, which are as follows :
Smaller and less robust, with much shorter antennae, which are a
little thickened towards the apex, the 3rd joint scarcely longer than
the 2nd, the 4th a little longer than the 3rd, the 5th to the 10th
gradually decreasing in length, conical. 8th to 10th only slightly
longer than broad, 11th ovoid, longer than the 10th.
New Species of Staphylinidae from Singapore. 237
Hab. Woodlands, Bukit Panjang and Bukit Timah, in
old logs.
52. Conosoma perplexum, n. sp.
Xeddish-testaceous, shining; the antennae pale testaceous, the
5th to the 10th joints infuscate; the elytra obscurely infuscate
posteriorly. Legs pale reddish-testaceous. Length 2°3 mm.
Of the build of C. suave, Fauv., but a trifle larger, the antennae
distinctly longer and differently coloured, the thorax without mark-
ings. Antennae extending a little beyond the posterior angles of
the throax, the 2nd and 3rd joints elongate, of equal length, the 4th
a little shorter than the 3rd, 5th to 10th subtriangular, compressed
laterally, subequal, scarcely longer than broad, the 11th long, oval,
considerably longer than the 10th. Thorax very finely and not very
closely punctured ; pubescence fine and yellow. Elytra a little longer
than the thorax, slightly narrowed behind, with puncturation and
pubescence as on the thorax; ground-sculpture very fine, feebly
imbricate; towards the apex (but not reaching the posterior border),
an indeterminate fuscous cloud is perceptible in certain lights.
Abdomen exceedingly finely and sparingly punctured, especially
posteriorly; ground-sculpture exceedingly fine and feebly imbricate ;
sides and apex setose; eighth dorsal segment divided into four
triangular processes by three triangular excisions.
Hab. Bukit Panjang, in rotten wood. One specimen.
53. Conosoma nigromaculatum, nh. sp.
Reddish-testaceous, shining, a subtriangular spot on either side
of the middle of the base of the thorax, a transverse patch nearly
reaching the lateral margins of the elytra externally, and the suture
internally, and the 6th to LOth joints of the antennae black. Sides
of the elytra each with six long setae. Length 2 mm.
Exactly of the build, and almost of the colour, of C. suave, Fauv.,
the head, however, is clear reddish-testaceous, the antennae are
shorter and differently coloured, with the 7th to LOth joints dis-
tinctly transverse, the elytra are rather longer than the thorax, and
furnished with long setae at the sides, and the 5th abdominal seg-
ment is scarcely infuscate. The antennae do not extend to the
posterior angles of the thorax, the 3rd joint is shorter than the 2nd,
the 4th scarcely longer than broad, the 5th as long as broad, stouter
than the 4th, the 6th scarcely transverse, the 7th to the LOth dis-
tinctly transverse, 11th, stout, short, oval. Thorax very finely and
not very closely punctured; pubescence fine golden yellow; on
either side of the middle line at the base is an indeterminate, more
938 Dr. Maleolm Cameron on
or less triangular dark spot. Elytra each with a transverse black
patch placed much nearer to the posterior than to the anterior
borders, and almost reaching the lateral margins externally and the
suture internally; puneturation and pubescence much as on the
thorax, the sides with six long black setae. Abdomen strongly
pointed, very finely and sparingly punctured, strongly setose. Legs
pale reddish-testaceous.
Hab. Woodlands and Bukit Timah, in old logs.
D4, Conosoma rufotestaceum, hn. sp.
Reddish-testaceous, shining; sides of the elytra strongly setose ;
the first four and the last joints of the antennae and the legs yellow
testaceous. Length 1:5 mm.
Build somewhat resembling that of C. monticola, Woll., but smaller
and with the sides of the elytra furnished with strong setae. Head
shining, reddish-testaceous, scarcely visibly punctured; pubescence
sparing, yellow, rather coarse. Antennae barely extending beyond
the posterior angles of the thorax, the 2nd and 8rd joints of equal
length, the 4th to the 6th a little longer than broad, gradually de-
creasing in length, the 7th as long as broad, the 8th to the LOth
distinetly transverse, the I1th short, oval. Thorax more than half
as broad again as long, clear reddish-testaceous, very finely and
sparingly punctured; pubescence yellow and rather coarse; the
sides without setae. Elytra distinetly longer than the thorax, as
long as broad, gradually narrowed posteriorly, the puncturation
and pubescence similar to that of the thorax; the sides each with
six long black setae, and the posterior margins narrowly and
obscurely infuscate. Abdomen strongly pointed, obscurely infus-
cate at the base, puncturation very fine and sparing, the sides and
apex strongly setose.
Hab. Woodlands, in old logs.
55, Coproporus rufiventris, 1. sp.
Pitchy, shining; the head, margins of the thorax, latera and apical
borders of the elytra very narrowly, and the abdomen, red; anten-
nae with the first four joints, and the apex of the last, testaceous
yellow; legs reddish-testaceous. Length 4:5 mm.
Rather broad, moderately convex, and, with the exception of the
abdomen, impunctate; the latter considerably narrower at the base
than the elytra, elongate, and rather strongly narrowed posteriorly :
of the build of C. brunneicollis, Motsch., but larger than that species.
a} ° . . . ” . ¢
New Species of Staphylinidae from Singapore. 239
Head transverse, pentagonal, ferruginous red, a narrow line between
the bases of the antennae and a short one in the middle of the front
portion of the vertex which joins the preceding, pitchy, the eyes
rather large and prominent, the temples converging posteriorly ;
glabrous, without trace of puncturation, very finely and transversely
strigose. Antennae rather short, the 2nd and 3rd joints subequal,
the 4th obconical, shorter than the 3rd, the 5th to the 7th cylindrical,
a little longer than broad, the 8th to the 10th as long as broad, the
11th rather stout, oval, as long as the two preceding joints together.
Thorax strongly transverse, widest at the posterior fourth, from
thence strongly rounded and narrowed in front to the rectangular and
prominent anterior angles, less strongly narrowed backwards to the
gently rounded posterior angles ; anterior border broadly emarginate,
posterior border sinuate on either side; sides and borders narrowly
but distinetly ferruginous red; the whole surface glabrous and
impunctate, very finely, and transversely strigose. Scutellum
impunctate, ferruginous. Elytra one-third as long again as the
thorax and of equal breadth, transverse; the sides feebly impressed,
the impression nearer the posterior angles; the suture and lateral
and posterior margins very narrowly ferruginous; surface glabrous,
impunctate, finely transversely coriaceous. Abdomen ferruginous
red, very finely and sparingly punctured, with short, fine, sparing,
yellow pubescence; ground-sculpture fine, coriaceous; 8th dorsal
segment in both sexes divided into four long triangular processes
(of which the central pair are a little longer than the lateral) by three
deep excisions, the apices of which are rounded.
$. Kighth ventral segment with a broad, deep, triangular excision
of the posterior margin.
®. Eighth ventral segment divided into five processes by four deep
excisions; the central process broad, narrowed a little towards the
apex, which is truneate with a small central notch; the lateral pairs
narrow and elongate, the most external of them a little shorter than
the rest, which are of equal length.
Hab. Bukit Timah and Mandai, in old logs.
56. Coproporus flavipennis, n. sp.
Black, shining, depressed; the first three joints of the antennae
and the extremity of the last, elytra, and legs testaceous. Length
2 mm.
Of about the size of the average C. melanarius, Er., but rather
more depressed, with much finer puncturation and differently
coloured elytra. Head formed as in melanarius, exceedingly finely
240 Dr. Maleolm Cameron on
and by no means closely punctured; ground-sculpture fine, trans-
verse, wavy. Antennae moderately long, longer than the head and
thorax, the 3rd joint as long as the 2nd, the 4th to the L0th not much
decreased in length, the 11th rather long, oval. Thorax built as in
melanarius, the posterior margin narrowly and obscurely testaceous,
the puncturation and ground-sculpture similar to that of the head.
Scutellum black, scarcely perceptibly punctured, finely strigose
transversely. Elytra yellow testaceous, about half as long again
as the thorax, very narrowly impressed along the lateral margins,
exceedingly finely and by no means closely punctured and without
trace of ground-sculpture, except some faint traces of longitudinal
striae towards the posterior margins. Abdomen very finely (but
more distinctly) and sparingly punctured ; ground-sculpture distinct,
transverse, strigose; sides setose; eighth dorsal segment divided
into four triangular processes (of which the median pair are longer
than the lateral) by three narrow triangular excisions.
2 (?). Sixth ventral segment with a broad, deep, oval excision
posteriorly.
Hab. Bukit Panjang, under bark. A single specimen.
57. Coproporus parvulus, n. sp.
Obscure rufo-testaceous, shining; the head, and the base and
more or less of the disc of the elytra, darker; first three joints of
the antennae and legs testaceous, the rest of the antennae scarcely
infuseate. Length 1:75 mm.
Of the build of C. minimus, Motsch., but smaller and narrower,
with the head and thorax impunctate and the elytra much less
distinctly punctured. Head pitchy-red, shining, impunctate.
Antennae not reaching the posterior angles of the thorax, and not
thickened after the 5th joint, the 3rd joint obconical, smaller and a
little shorter than the 2nd, the 4th slightly longer than broad, the
5th as long as broad, the 6th to the 10th gradually shorter, the 11th
conical. Thorax glabrous and impunctate. Elytra about one-third
longer than the thorax, narrowed posteriorly, the sides distinctly
impressed from the postero-external angle to near the antero-
external angle; puncturation very fine and indistinct, evanescent
posteriorly. Abdomen rufo-testaceous, exceedingly finely and
sparingly punctured, pubescence short, yellow, sparing; sides and
apex with long black setae.
Hab. Woodlands.
New Species of Staphylinidae from Singapore. 241
MiIMocyYPTUS, n. gen.
Minute, strongly convex, contractile, in facies very similar to
Hypocyptus. Head transverse, deeply inserted in the thorax.
Antennae I1-jointed. Mandibles short and stout, obscurely serrate
towards the apex of their inner margin. Inner lobe of the maxilla
narrow, with pectinate inner margin; outer lobe broad, obtriangular,
furnished with long setae on the distal margin. Maxillary palpi
with the Ist joint very small, the 2nd curved, much larger and stouter,
the 3rd a little longer than the 2nd, enlarged towards the apex, the
4th as long as, but narrower than the 3rd, conical. Mentum (pars
antica) transverse, quadrangular, narrower at the anterior than at
the posterior border, which are both truncate. Labium transverse,
narrower in front, quadrate. Labial palpi 3-jointed, the Ist joint
short and stout, broader than long, the 2nd smaller and shorter than
the Ist, broader than long, the 3rd much narrower than the preceding,
as long as the first two joints together, almost cylindrical. Tongue
broad, membranous, rounded, deeply and triangularly emarginate
in front, almost bilobed. Paraglossae distinct, pectinate, extending
slightly beyond the anterior margin of the tongue. Thorax strongly
transverse, convex, overlapping the elytra when the insect is ex-
tended; the anterior margin broadly emarginate, the sides strongly
rounded, passing insensibly into the base, the anterior angles obtusely
rounded. Prosternum small, the episterna much abbreviated, the
epimera free, elongate as in T'achinus. Anterior coxae contiguous, as
long as and larger than the femora. Mesosternum broadly and deeply
emarginate in front; the middle coxal cavities completely separated
by a very narrow mesosternal process. Metasternum bisinuate at
the posterior margin, the posterior coxae contiguous. Elytra extend-
ing beyond the metasternum, finely bordered at the sides; the
epipleura incomplete and quite invisible when viewed from the side.
Tibiae setose. Tarsi all 5-jointed; the anterior pair with the first
four joints short, triangular, emarginate at the distal margins, the
4th joint smaller than the preceding; the middle pair with the Ist
joint elongate as long as the two following joints together, the 2nd
and 8rd of equal length, each a little longer than broad, the 4th
smaller than the 3rd, the 5th elongate, nearly as long as the three
preceding together; the posterior pair similarly formed to the inter-
mediate; the claws all simple. Abdomen short, conical, retractile,
narrowly margined.
58. Mimoeyplus globulus, n. sp.
Strongly convex, shining, ferruginous red, the fore-parts impunc-
tate, the abdomen scarcely perceptibly punctured, very finely and
242 Dr. Malcolm Cameron on
sparingly pubescent; antennae with the first four joints and the
apex of the 11th, the mouth-parts, and legs testaceous. Length
1-2 mm. (in well-extended examples).
Head large and transverse, ensconced in the thorax, the eyes large
and rather prominent; entirely impunctate, and without ground-
sculpture, practically glabrous (under a high magnification a few
very fine short hairs are visible). Antennae with the first two joints
rather stout, the 2nd joint a little longer and not so thick as the
Ist, the 3rd joint as long as the 2nd, the 4th, 5th and 6th each a little
shorter, the 7th to 10th transverse, 7th to 11th forming a club, 11th
oval, as long as the two preceding together. The thorax has been
sufficiently noticed in the generic characters give above: it is
broader than the elytra, the base of which it overlaps, and like the
head is impunctate and practically glabrous. Elytra longer than
the thorax and about as broad as long, a little narrowed behind and
truncate, and like the head and thorax almost glabrous and impunc-
tate. Abdomen short, conical, finely bordered, retractile, scarcely
perceptibly punctured, with short, fine, and sparing yellow pubes-
cence, and scarcely visible transverse ground-sculpture; the sides
and apex furnished with long black setae.
g. Eighth dorsal segment simple; 6th ventral segment with a
rather deep triangular excision of the posterior margin.
®. Eighth dorsal segment divided into four pointed triangular
processes by three triangular excisions, of which the lateral ones are
a little deeper than the others, the middle processes each with a short
yellow seta, the lateral ones each with a long black seta.
Hab. Keppel Harbour, in débris.
ADINOPSINI, n. group.
ADINOPSIS, n. gen.
Antennae with the 11th joint furnished with a slender, subulate,
accessory joint nearly as long as itself. All the tarsi 2-jointed ( ?).
I am unable to give more details of this remarkable
genus owing to lack of material. The species on which
it is founded has the facies, puncturation, pubescence, and
labial palpi of Dinopsis, but I believe that all the tarsi are
composed of two joints only. The characters given would
appear to necessitate the erection of a new group, the
‘* Adinopsini.””
New Species of Staphylinidae from Singapore. 243
59. Adinopsis rufobrunnea, n. sp.
Minute, obscure reddish brown, the elytra (in one specimen) and
the first four visible segments of the abdomen blackish; densely
and finely punctured and pubescent throughout, scarcely shining ;
antennae, mouth-parts and legs testaceous. Length 1-4 mm.
Similar in scheme of coloration to D. cinnamomea, Kr., from Ceylon,
but much smaller and narrower. Head transverse, convex, the eyes
small, the temples passing insensibly into the base; puncturation
exceedingly fine and close, pubescence very fine. Antennae long
and slender, the Ist and 2nd joints of about equal length, stouter
‘than the following, the 3rd shorter than the 2nd, the 4th longer than
the 3rd, the 4th to the 11th all elongate and differing but little in
length, the 12th slender, subulate, almost as long as the I1th.
Thorax transverse, convex, widest posteriorly at the rectangular
posterior angles, from thence gently rounded and narrowed to the
obtuse anterior angles; posterior margin bisinuate, making the
hind angles a little prominent; puncturation close, fine, but rather
rough, pubescent fine, yellowish. Scutellum concealed. Elytra
about as long as, but narrower than, the thorax, transverse, pretty
deeply emarginate internal to the postero-external angles, from
thence obliquely truncate to the suture; puncturation and pubes-
cence similar to that of the thorax. Abdomen pointed, margined,
the first four visible segments blackish, the last two reddish-testace-
ous; puncturation dense and fine, more sparing on the last two
segments; pubescence dense and fine, almost sericeous; anal styles
of equal length, the lateral stouter than the median. Sides of the
abdomen and tibiae not setose.
Hab. Sembawang, in flood débris. Two examples.
GYMNUSINI.
60. Leucocraspedum nigrum, n. sp.
Black, convex, pointed posteriorly, shining, finely and closely
pubescent; antennae short, testaceous yellow, the last two joints
infuscate; legs pitchy-testaceous. Length scarcely 3 mm.
Head transverse, deflexed, shining, scarcely visibly punctured ;
eyes rather large. Antennae short, the Ist and 2nd joints of equal
length, the 3rd shorter and narrower than the 2nd, the 4th and 5th
decreasing in length, a little longer than broad, the 6th to the 10th
gradually more strongly transverse, the I1th elongate, nearly
equal to the three preceding together. Palpi testaceous. Thorax
transverse, considerably narrowed in front, the sides passing insen-
244 Dr. Maleolm Cameron on
sibly into the convex anterior margin, widened behind, the posterior
angles a little prominent, rectangular, the base bisinuate; punctura-
tion very fine and close ; pubescence fine and close, greyish; scutellum
concealed by the thorax, which overlaps the base of the elytra.
Elytra shorter than the thorax (measured along the suture), trans-
verse, a little emarginate internal to the postero-external angles,
obliquely truncate to the suture; puncturation very fine and close,
but not so fine as that of the thorax; pubescence fine and close.
Abdomen elongate, strongly pointed posteriorly, uniformly punctured
similarly to the elytra and with similar pubescence; the sides and
apex with long black setae, the dorsal surface with a row of erect
setae on either side.
Hab. Bukit Panjang, in rotten logs.
MYLLAENINI.
61. Myllaena faberensis, n. sp.
Narrow, elongate, acuminate, blackish, the thorax, elytra, posterior
margins of the first four visible and the whole of the 7th and 8th
segments reddish-testaceous; antennae, mouth-parts, and legs
clear testaceous. Length 3-4 mm. ,
In build and structure of the antennae similar to WM. tenuicornis,
Fauv., of Europe. Head blackish, very finely punctured and
pubescent, moderately shining. Antennae slender with all the
joints elongate, the 2nd longer than the Ist and 3rd, the 3rd to the
6th of equal length and breadth, the 7th to the 9th a little shorter,
equal to each other, the 10th a little shorter than the 9th, the 11th
elongate, pointed, a little longer than the 10th. Thorax feebly
transverse, broadest about the middle, from thence the sides gently
rounded and narrowed to the anterior angles, very slightly narrowed
and scarcely at all rounded to the rectangular posterior angles, the
base lightly bisinuate; puncturation exceedingly dense and fine;
pubescence fine, short, dense and yellowish. Elytra transverse,
scarcely as wide as, and a little shorter (measured along the suture)
than, the thorax; posterior margins obliquely truncate from the
postero-external angles, which are emarginate internally ; punctura-
tion and pubescence exceedingly dense and fine as on the thorax.
Abdomen elongate, pointed, exceedingly densely punctured and
pubescent, sericeous; sides and apex with moderately long black
setae. Middle tibiae with a short weak seta at the middle of the
outer border.
Hab. Mount Faber.
New Species of Staphylinidae from Singapore. 245
PRONOMAEINI.
62. Pronomaea leontopolitana, n. sp.
Chestnut-brown, rather shining, the fore-parts finely and closely
punctured; antennae fuscous, the first two joints, palpi, and legs
testaceous. Length 3 mm.
More robust than P. rostrata, Er., with stouter antennae, closer
puncturation, and thorax more contracted at the base. Head round,
the eyes large; closely and finely punctured and pubescent. Anten-
nae long and stout, the Ist and 2nd joints of equal length, the 3rd
longer than the 2nd, the 4th a little longer than broad, the 5th as
long as broad, the 6th to the 10th transverse, but not strongly so and
not increasing appreciably in width, the 11th shorter than the two
preceding together. Thorax transverse, broadest at the middle,
the sides from here gently rounded and converging to the anterior
angles, and posteriorly more strongly retracted in a straight line to the
obtuse posterior angles; the disc in the middle line before the base
with a well-marked impression and between this and the posterior
angles is a rounded fovea; puncturation fine and rather close ;
finely pubescent. Elytra broader than, and as long as, the thorax,
transverse, strongly emarginate internal to the postero-external
angles, finely and rather closely punctured and pubescent. Abdomen
shining, finely and very sparingly punctured and pubescent.
Hab. Mandai, Bukit Timah, in damp débris.
DIGLOTTINI.
63. Diglotta testaceipennis, n. sp.
Linear, pitchy, abdomen black, scarcely shining, densely and
finely pubescent; antennae, elytra, legs, and last abdominal segment.
testaceous. Length 1-5 mm.
Head large, round, depressed, impressed on the vertex; the eyes
small, the temples large; sculpture exceedingly fine and close; no
definite puncturation visible. Antennae with the Ist and 2nd
joints of equal length, the 3rd much shorter, the 4th, 5th, and 6th
cylindrical, a little longer than broad, the 7th to the 10th as long
as broad, the 11th oval, pointed. Thorax scarcely transverse, a
little broader than the head, widest just behind the anterior angles,
from thence lightly rounded and narrowed anteriorly, contracted
posteriorly in a nearly straight line to the obtuse posterior angles ;
the disc lightly and broadly impressed along the middle; exceedingly
finely and closely sculptured, finely pubescent. Elytra as broad as,
246 Dr. Malcolm Cameren on Siaphylinidae from Singapore.
and one-third longer than, the thorax, parallel, longer than broad,
densely and finely sculptured and pubescent. Abdomen black, the
apex reddish-testaceous, parallel, very finely and closely punctured
and pubescent throughout.
Hab. Pasir Panjang. Two examples on the beach, one
under a stone below high-water mark, the other in a rotting
pine-apple.
XIV. Notes on Australian Sawflies, especially the “ Authors’
Types” and other specimens in the British Museum
of Natural History and the Hope Collections of
the Oxford University Museum; with diagnostic
Synopses of the Genera and Species, and photographs
dlustrating their structural characters. By the Rev.
Francis Davip Moricg, M.A., F.Z.S.
[Read October 2nd, 1918.]
PLATES: XI-XYV,
INTRODUCTORY.
THIS paper—the first in which I have ventured to treat of
other than Palaearctic insects—is the result of an oppor-
tunity so exceptional that it seems almost a duty to make
use of it. For a considerable time this year I have had
continuous access in the British Museum of Natural History
(a) to the entire “literature” of my subject, and (6) to
very nearly the entire material on which that literature
is based. The first Sawflies described from Australia were
Plerygophorus cinctus and interruptus of Kluge (1812), and
the Types of these—presumably still at Berlin—were, of
course, inaccessible to me. But almost all Australian
genera or species since described were founded on specimens
still preserved either in the Museum above mentioned
(which shall hereinafter be denoted by the initials B.M.),
or in the Hope Collections of the Oxford University Museum:
and, through the kind assent of Professor Poulton to an
application which I made to him, all specimens of Australian
Sawflies in the latter Collections were temporarily entrusted
to me for study and comparison with the material already
before me in B.M.
This means that I have been able to examine at leisure
and with every facility that could assist me at hand (a) the
original author’s Types (and sometimes also Co- -types) of
all forms deseribed by Leach in 1817, Westwood in Arcana
Entomologica (1841) and Proc. Zool. Soc. Lond. (1880),
W. F. Kirby in his British Museum Inst and various later
‘Separata ’ (1881 to 1894), Gilbert Turner in Proc. Linn.
TRANS. ENT. SOC. LOND. 1918.—PARTSIIL,IV. (MAR.'19)
248 Rev. F. D. Morice’s Notes on Australian Sawflies.
Soc. N.S. Wales, (1900), and 8. A. Rohwer* in Ent.
News, Philadelphia (1910). The B.M. Coll. contains also
specimens of the remarkable genera Philomastix and
Phylacteophaga, Froggatt (Proc. Linn. Soc. N.S. Wales,
1890 and 1899). These are not actually Types, but
were all either determined by the author, or received
from the same source as his Types.f Other interesting
material which I have examined in B.M. includes many
specimens of new or little-known Australian forms presented
by Mr. Rowland Turner, and a Plerygophorus received early
in the present year (1918) from Mr. Frogeatt, which 1s
evidently the bifasciatus of Brullé, and the only example
of that remarkable species that has occurred since the
original Type was described more than seventy years ago.
In spite of Konow’s a priori reasonings to the contrary,
this species is most certainly a Plerygophorus and one of
the most beautiful representatives of that beautiful genus.
Besides the above Australian material I have been able
to examine in the B.M. and Oxford Collections many
Types of exotic genera and aeaces s described by Westwood,
F. Smith, W. F. Kirby, Cameron, ete., some of which,
though not belonging to the Australian Fauna, seem allied
to certain of its genera by the possession of several very
abnormal and even paradoxical characters. Most of these
insects are from South or Central America, a circumstance
which will require consideration presently.
Apart from this great advantage of access to so many
* Mr. Rohwer kindly communicated to. me, while these Notes
were still in MS., a type-written copy of a Paper which has since
appeared in Ann. and Mag. Nat. Hist. (Nov. 1918), containing
descriptions of a new genus (Zenarge) and three new species. The
Types of these are still in America, having been sent there from
B.M. for determination by Mr. Rohwer in 1915. Duplicates, how-
ever, except in one or possibly (?) two cases, were retained in the
Museum; and I had already dealt with these in my Tables, and given
them names for which I now substitute those published by Mr.
tohwer.
+ The Type-species of Philomastix (glabra) is figured and described
by Westwood as * Perga (sic) macleayi,’ from two 2 specimens
at Oxford, both of which had lost their antennae before Westwood
saw them. Otherwise he would, of course, have seen that the
species could not be a Perga. This insect must in future, [ suppose,
be called Philomastix macleayi, Westw.
t The vessel conveying this precious specimen was torpedoed
en route! But the insect, though literally drenched with a mixture
of sea-water and naphthaline, is still perfectly recognisable, and for
practical purposes little the worse for its adventures.
Rev. F. D. Morice’s Notes on Australian Sawflies. 249
Types, the want of which access has greatly impaired the
value of much recent work * on Australian forms, L have
been singularly fortunate in being occupied on these
investigations exactly when and where I could at once
take counsel on any difficulty that might arise with a
colleague who, of all men, was perhaps the best qualified
to assist me. Mr. Rowland KE. Turner, well known to all
Hymenopterists as the author of many important memoirs
on various groups of exotic Aculeates, had long devoted
himself to voluntary work in arranging and augmenting
the B.M. collections of Hymenoptera, and had lately
received a formal appointment as an honorary member of
the Museum Staff. He had previously resided for twenty
years in North Queensland, and both there and in other
parts of Australia (Swan River, Tasmania, the neighbour-
hood of Sydney, etc.) made large entomological collections,
all which he has now presented to B.M. Though more
specially interested in other groups, he had by no means
neglected the Sawflies—in fact, several Australian species
and at least two genera are known to me only through
his captures. Being myself almost entirely ignorant
of “exotic ’’ insects, Hymenopterous or otherwise, and
having only the vaguest ideas about the geography,
physical features, climate, seasons, etc., etc., of the Aus-
tralian “‘ Realm,” I naturally seized every opportunity
of profiting by Mr. Turner’s familiarity with all these
subjects, and though I cannot regret that I have done so,
I am conscience-stricken when I think how unscrupulously
I have exploited his good nature.
I have also to thank an American colleague, Mr. 8. A.
Rohwer of Washington, for several very kind and en-
couraging letters, and for communicating to me unpublished
notes of his own on some of the specimens which I have
examined, as well as for copies of many of his Separata,
especially his Classification of the Suborder Chalastogastra
(Proc. Ent. Soc. Washington, 1911) and Genotypes of the
Sawflies and Woodwasps (U.S. Dep. Agric., Technical Series
No. 20, Part IT, Washington 1911).
The Figures illustrating this paper are reproductions
* H.g. Konow’s attempts to classify the known species of Perga
and Pterygophorus. Having in most cases only old and inadequate
diagnoses and figures to euide him, he naturally made many mistakes
both in identifying species, and in deciding where to place them in
his Tables.
250 Rev. F. D. Morice’s Notes on Australian Savwflies.
of photographs (or in a very few cases of drawings) taken
by myself from B.M. or Hope Coll. specimens, the parts
figured having nearly always been prepared bys. Vins WAG
Cant, F.E.S., in the Museum “ Setting-room ”’ by the kind
permission of Dr. Gahan or Professor Poulton. I am
greatly indebted to Mr. Cant for the invaluable assistance
I have received from him in this matter, and am glad to
think that his preparations will henceforth be a part (and,
I think, a very useful part) of the CoHections at Oxford and
South Kensington. The photographs representing details
of saws in the. various species of Perga and X: yloperg ga were
all taken at the same magnification, but this is not the
case with the other figures. It will be noticed that in some
of those representing antennae the two short basal joints
are missing, but these joints are not particularly character-
istic, and their omission is therefore of little consequence.
When these notes were commenced, and even after con-
siderable progress had been made with them, they were
intended merely as materials for a revision of the Genus
Perga. But I afterwards resolved to adopt a suggestion
made to me by Mr. Turner that they should include also
some account of such other Australian Sawfles as were
represented in the Collections to which I had access. The
materials available for this part of my work were quite
insufficient for the clearing up of many questions, which,
as long as they remain unsettled, will render the production
of anything that deserves to be called a “ Monograph”
impossible. Still, as I have seen all the Types of described
species in some genera, and either Types or specimens
which I have reason to believe are correctly named in all
but one of the others, it seems worth while to indicate in
tabular form the characters by which they seem most easily
distinguishable in the specimens before me, even when I
cannot be sure that these characters are of specific value.
Accordingly I have prepared dichotomic Tabulations
or Synopses, first of the genera, and afterwards of the
species in each genus of which more than a single species
is known. Except in the cases of Perga and Pter ‘ygophor US,
where some trouble has been taken to make the order in
which the species are arranged correspond to my idea of
their natural affinities, I have aimed in these Synopses
at nothing more than to facilitate the naming by collectors
of their specimens, and have employed indifferently what-
ever characters, whether of structure or merely of colora-
Rev. F. D. Morice’s Notes on Australian Sawflies. 251
tion, seemed likely to be recognised most easily. It is
quite possible that some of these characters are merely
“individual,” but of this there is always a chance when
attempts are made to diagnose the characters of a species
from a single specimen.
I will now give my Synopses of Genera and Species, and
these will be followed by a few detached Notes, or
‘ Excursuses,”’ dealing with various questions which came
up for consideration as my work proceeded. These are
mere Tentamina, and probably very crude, for they often
touch on subjects with which my acquaintance is very
recent. But it has interested me to write them, and I hope
no harm will be done by publishing them in their present
shape.
SYNOPSIS OF THE GENERA.
(Genera marked thus + cannot be considered as indigenous. )
1. Antennae (see Figures in Plate X LI, Figs. 1, 2) inserted close to the
mandibles—lower down in the face than the lowest part of
the eyes.* On each side of the head above (very near each
eye) runs a series of little tubercles. Middle and hind tibiae
denticulate along their hind-margins (Pl. XII, Fig. 18). The
° hypopygium appears as a sort of compressed longitudinal
carina (in the middle of the 5th ventral segment). In the lateral
view it is tooth-like (subtriangular); and beyond it is seen
the exposed part of the paradoxically long and _ slender
* terebra ” or boring-organ (a modified ovipositor), resembling
merely a fine hair, unless really highly magnified, when the
apices of its paired “ spicula”’ are seen to be armed with a
very few minute teeth. (Its structure and attachments are
very like those of the corresponding organ in a Cynipid /)
Cf. Figs. 1, 2,3in Pl. XII. In the ¢ the apex of the abdomen
is simply convex above and below. The labial palpi are
short, 3-jointed; the maxillary palpi much longer, 5-jointed.
Kach fore-leg has one calear only; each posterior leg
has fwo, but one of them is so short that it may easily be
overlooked. Neuration of wings very incomplete. The
antennae have 12 joints in the 9, 11 in the 3.
(F arly ORYSSIDAE. ) Genus I. CREEL ODES: Konow.
* Hartig and others say “below the clypeus, 5 but what they
take for the clypeus is in this case really a part of the SpnGee alr
developed *frons.” The true clypeus is to be found lower down,
between the insertions of the antennae and the mouth-parts, as in
all Hymenoptera (I believe) without exception !
252 Rey. F. D. Morice’s Notes on Australian Sawflies.
[The only Australian species is O. sericatus, Mocsary,
described in Term. Fiiz. (Feb. 1900) from New South Wales.
In the same year but some months later Mr. Gilbert Turner
described the same species from Mackay, North Queensland,
under the name Oryssus queenslandensis. The Type of
queenslandensis, G. Turner (and many other specimens 3 and
2 from Kuranda, N. Queensland),* are in B.M., but not the
Type of sericatus, Mocs. In this species the fore-wing of
the 2 is crossed by two conspicuous dark clouds, in the 6)
wing these are scarcely indicated (Pl. XI, Figs. 1 and 2).|
— Insertions of antennae between the eyes, never below them, and
separated from the mouth-parts by a visible “ clypeus.”
Top of head with no lateral rows of tubercles. Neuration of
wings more or less complete, always with at least 3 closed
cubital cells in each fore-wing. . . . . . . oe 4
2. Front tibiae with only one apical spine or “ calear.”’ herent
many-jointed, long, slender, and filiform, with simply cylin-
drical joimts (none of them dilated, pectinated, bifurcated
or otherwise paradoxically developed in either sex). The
dorsal apex of the abdomen is generally more or less acuminate,
and in the 9 the ovipositor projects from below it (looking
like a stout needle with a blunt point). The scutellum is not
distinctly separated from the rest of the mesonotum.
(Family SIRICIDAE). 3.
— Front tibiae with two calcaria. Antennae with the joints
seldom quite simple. (Often they are clavate, capitate,
pectinate, serrate on one side, pilose, ete., etc., see Pl. XII,
Fig. 1 to 11.) Ovipositor of 2 usually concealed within a bi-
valved chitinous sheath, which is always visible from beneath,
and may (or may not) project slightly beyond the dorsal apex
of the abdomen. Scutellum always distinctly separated from
the rest of the mesonotum . (Family TENTHREDINIDAR). 4.
3. Costal area of fore-wing (7. e. the space between the costa and
subcosta) divided by a longitudinal ** vein,” but with no
“nerve” crossing it transversely. Last dorsal plate of the
abdomen in the 2 deeply foveated before its apex, which is
compressed and drawn out into a straight nail-like process,
from beneath which the ovipositor may be seen projecting.
The latter is much stouter than that of Ophrynopus, but the
structure in both cases is essentially the same.
* These specimens were all taken by Mr. R. E. Tea emerging
from holes apparently made by be etles in a dead Eucalyptus tree
in June or July !
Rev. F. D. Morice’s Notes on Australian Sawflies. 253
The only species recorded from Australia (australis,
W. F. Kirby = juvencus, L. !) is certainly a mere accidental
importation from the Northern Hemisphere, and no part
of the true indigenous Fauna. The 9 is chalybeous (blue
with green and purple reflections). The ¢ has a shining
testaceous abdomen, and the legs are mostly black, while
those of the 2 are mostly yellowish. In both sexes the
bases of the antennae are testaceous. (The Type of
* australis ’—a Q—is in B.M.)
72. Strex, L. (= Paururus, Knw.).
— Costal area of fore-wing crossed by a transverse “nerve,” but
without a longitudinal * vein.”
Mr. Rohwer has described in Ann. and Mag. Nat. Hist.
(Nov. 1918) a new species of this genus from North Queens-
land (obtusiventris, Rohw. 2). I have not seen the unique
Type, but it is described as black with antennae and legs
ferruginous; 8 mm. long; with the abdomen “rounded
not tapering apically,” this being a very unusual character
in a Xiphydria. (As the species does not seem to have
occurred elsewhere it is presumably indigenous.) For a
full account of its other characters see the author's
deseniption.(lc.). .. . . . . 3. XipHypri, Latr.
4. Middle and hind tibiae with calcar-like spines before as well as
at their apices (PI. XIV, Fig. 19, Pl. XV, Fig. 19) ..° 2 « 5.
— Middle and hind tibiae with no spines other than the apical
CHICA ge ce a Pere ce yk hg ew Me ee
5. Antennae apparently only 3-jointed (all joints beyond the two
short basal ones being fused together and not distinguishable).
Fore-wings with a distinct ** lanceolate cell” (Pl. XI, Fig. 3).
(Subfamily Arginae). 6.
— Antennae with at least 5 distinct joints. Fore-wings without a
lanceolate cell, the humeral nerve being undeveloped. (Mr.
Rohwer divides the genera of this section between two of
his ‘‘ Families ’’—the Perreyiidae and the Pergidae, placing
Philomastix and Phylacteophaga in the former, Perga, X yloperga
and Cerealces in the latter, but for certain reasons I hesitate
at present to take this view, and prefer to leave their precise
afmmipies tndecided.” . Galas 9s 2a + 6) oe ee Se
6. Lanceolate cell crossed obliquely by a transverse nerve.* © Hind-
* This character does not occur in any other genus of the Arginae /
254 Rev. F. D. Morice’s Notes on Australian Sawflies.
wings with only one closed cell, a cubital. Middle tibiae
(PI. XII, Fig. 19) with two (!) spines before their apices, hind
tibiae with only one. Antennae of the ¢ simple (not furcate)
and scarcely if at all more pilose than in the 9 (see Pl. XII,
Fig. 4), and for a full description of the only species (turner?,
Rohw n. sp.) ef. the author’s account of it in Ann. and Mag.
N. H. (lic.) . .. 1 . . 4 ZENARGE, Rohwer, nov. gen.
— Lanceolate cell ** contracted ” asin Arge, Schrank (= Hylotoma,
Auctt.) Hind-wings with two closed cells, a cubital and a
medial. Antennae of g much more as than those of
the ON a ee ee eee ee ee 5 te Mois
7. Only 3 complete cubital cells in the fone wing (the Ist cubital
nerve being absent or represented by a mere rudiment).
In the hind-wing the recurrent nerve lies beyond the cubital
(7. €. nearer to the margin of the wing). The last joint of the
6 antennae is furcate (Pl. XII, Fig. 3).
5. TricHornacuus, W. F. Kirby.
[For Synopsis of the species see p. 259. |
— Four complete cubital cells in the fore-wing. In the hind-wing the
recurrent and cubital nerves are “interstitial”? (Pl. XI,
Fig. 4). The last joint of the ¢ antenna is not fureate.
6. ANTARGIDIUM, n. g.
The only known species of this genus (apicale, W. F.
Kirby) was described by its author (Ann. and Mag. N. H.,
July 1894) as a “ Hylotoma” (i.e. Arge!). But I venture
to think that it is better to ea it as a new and distinct
genus. Not only is it very much smaller than any of the
other forms at present referred to Arge, but it differs from
all other Arginae in the neuration of the hind-wing. In
none of these are the recurrent and cubital nerves inter-
stitial; and in all (except Trichorhachus) the cubital lies
beyond the recurrent, and so is nearer to the margin of the
wing !
8. (5) Antennae never with more than 7 distinctly separated joints,
usually with less, and either “‘ clavate’ from the 3rd joint
to the apex (Pl. XV, Fig. 18), or “ capitate,” 7. e. with the
apical joint only swollen into a club (Pl. XV, Fig. 20). Apex
of scutellum angled at each side and somewhat reflexed, the
angles usually forming little lobate (knob-like or tooth-like)
projections (= the “scutellar lobes”). .- . . . . QY.
— Antennae with more than 7 distinct joints, neither capitate
nor clavate, but with the apices of all joints except the two
Rev. F. D. Morice’s Notes on Australian Sawflies. 255
first and the last lobately produced in the 33 and angularly
projecting (“subserrate”)inthe9Q9 . . . . . . 10.
9. Antennae always capitate, with six joints preceding the club,
all distinctly separated from it and from one another. Labial
palpi with 4 joints, maxillary with 6, the former much thicker
than the latter.
7. XYLOPERGA, Shipp = Hepracoia, Konow.
[For Synopsis of the species see p. 265.]
— Antennae either capitate, or (in Kirby’s Section II of the genus)
clavate from the third joint to the apex. In both cases only
‘ejoints at most (in one species only 4) precede the apical
joint. Labial palpi with only 3 joints, maxillary with
only 4, the latter scarcely differing in thickness from the
iOUMCU Ewe tL ee gl ee Le Pima? Reach:
[For Synopsis of the species see p. 265.]
10. Antennae 8-jointed, long and slender; joints 4 to 7 produced
at their apices in the 3 into pointed lobes; in the 9 they are
nearly simple. Palpi as in Perga (labial 3-jointed, maxillary
4-jointed). In the fore-wings the Ist recurrent nerve is
sharply (angularly) bent in the middle, and runs very obliquely
into the cubital vein half-way between the Ist and 2nd cubital
nerves; the 2nd recurrent is straight, and nearly interstitial
with the 2nd cubital nerve. 9. PHyLAcTEOPHAGA, Froggatt.
[The only known species of Phylacteophaga is eucalypti,
Froggatt, described in Proc. Linn. Soc. N.S. W., Vol. 14
(1899). |
— Antennae with at least 10 joints. Both recurrent nerves are
straight and neither is interstitial . . . . . . IOI.
1]. Antennae in the ¢ (the other sex is unknown) 10- to 12-jointed,
the intermediate joints short and stout with dilated apices.
Scutellum coarsely and rugosely punctured, dull, bisected
by a sharply-defined longitudinal narrow suleation, its apex
produced into lobes as in Perga and Xyloperga, but here the
lobes are proportionately longer and more sharply pointed.
10. CerEaLces, W. F. Kirby.
[For Synopsis of the species see p. 287. |
— Antennae with at least 15 joints, these in the 3 resembling those
of Cerealces scutellata. In the 2 the antennae are con-
siderably longer than in the 3, the post-basal joints are slender
and elongate, but those following become shorter and broader
as they approach the apex. The scutellum is somewhat
shining, its disc in certain aspects appears bituberculate,
but it is not (as in Cerealces) divided by a sharp central
256 Rev. F. D. Morice’s Notes on Australian Sawflies.
furrow, its apex is simply rounded with no projecting
“lobes.” Fore-wings with the Ist cubital cell very short
and not completely closed, the very oblique Ist cubital n.
breaking off short without reaching the cubitus. In the 9
there is a conspicuous dusky fascia beneath the stigma
(Pl. XI, Fig. 13). Labial palpi 3-jointed, maxillary palpi
4-jointed (Pl. XII, Fig. 15). . 11. PHrtomastrx, Froggatt.
[For Synopsis of the species see p. 287. |
12. (4) Lanceolate cell absent, as in Perga, etc. . . . . 13.
— lanceolate cell present... . . . Whe Teas I:
13. Antennae only 7-joimted, the intermediate joints all short and
dilated towards their apices, forming together with the apical
joint a sort of club. Fore-wings with one radial cell and four
complete cubital cells, the second and third each receiving a
recurrent nerve. Hind-wings with one closed cell (a cubital).
Clypeus remarkably short and transverse, with the antennae
(as in Diphamorphus, vide infra) inserted just above it, and
therefore low down in the face. Scutellum punctured, sub-
triangular with a rounded apex and a narrow elevated margin.
12. PERGULA, n.g.
Type Pergula turnerit, n. sp. [For description see
p. 288. ]
(I do not know to what Subfamily this little insect should
be referred. The specimen is unique, and I have not been
able to dissect out the palpi. In certain characters it
resembles a very diminutive Perga, but the posterior
tibiae have no ante-apical spines.)
— Antennae multiarticulate. In all $4 and some 9 they are
pectinate (the pectination single—not, as in Palaearctic
“ Lophyrus,’ Auctt., double /), but in most of the 99 they
are merely serrate. Fore-wing with the 2nd cubital nerve
entirely wanting, so that the 2nd and 3rd cubital cells combine
to form a single long cell which receives both recurrent nerves.
13. PreryGorHorus, Klug.
(Subfamily ?). [For Synopsis of the species see p. 289. |
14. Radial cell divided by a transverse nerve.
The only species having this character yet recorded from
Australia is an undoubted alien, imported accidentally along
with the fruit-trees (Pyrus, etc.) on which it feeds. It is a
well-known pest in all parts of Europe and North America.
The lanceolate cell is not petiolate, but is crossed by an
Rev. F. D. Morice’s Notes on Australian Sawflies. 257
oblique nerve. The hind-wing has sometimes two closed cells,
sometimes only.one. .. . . = |. 14. Cariroa, Costa
= Eriocampa, Auctt. = Eriocampoides, Konow.
— Radial cell undivided. Lanceolate cell with no nerve crossing
it, but “petiolate.” Hind-wing never with more than one
Closedgeell ¥(Cuoitalisc I meme eo wee se cee? Se) LD:
15. Antennae pectinated as in Plerygophorus but far less closely,
the joints (apart from their branches) being longer. In the
3 of the only described species, viz. P. atratus, W. F. Kirby,
the antennae are 18-jointed. The @ is described by Mr.
tohwer in Ann. and Mag. N. H. (1.c.) from a specimen seen
by him in B.M., but this, I fear, has since been destroyed or
lost, for neither Mr. Turner nor I have been able to find it.
Its antennae were broken from the 12th joint onwards, but
each of the remaining joints after the second had “a ramus
like Pterygophorus.” Mr. Rohwer places it in his Subfamily
“ Huriinae,’ and compares its wing-veining to that of the
American genus Perreyia. (Kirby also brings Perreyia,
Eurys and Polyclonus near together, including them all in
the “Subfamily ” which he calls Lophyridinae.*)
15. Potycitonus, W. F. Kirby.
— Antennae without pectinations, nearly simple (or, at most, sub-
serrate) in both sexes (Pl. XII, Fig. 11). oe eee ede Os
3. Antennae inserted low down on the face, just above the short
transverse clypeus, and so not far from the labrum. Man-
dibles long and faleate, not toothed before the apex.
|
16. DipHamorRPHos, Rohwer.
[For Synopsis of the species see p. 294. |
— Insertions of antennae situated normally, 7. e. considerably
above the base of the clypeus, and nearly in the middle of the
PACE #2 estat ree fem Bre es te tay iad ws WO ae TINE
17. In the fore-wing the apex of the obliquely truncated radial
cell is separated from the margin of the wing by a distinct
(subtriangular) appendicular cell.
17. Eurys, Newman = Huryopsis, W. F. Kirby.
The general coloration of all the known forms is metallic
(aeneous, cupreous, or chalybeous). The antennae are
said to be always 9-joimted, and I have found them to
be almost invariably so in 2 specimens. But out of four
* T do not understand the formation of this word. Did the
author, perhaps, mean to write “ Lophyrinae” ?
258 Rev. F. D. Morice’s Notes on Australian Sawflies.
$3 in B.M. Coll. referred by Mr. Rohwer to his “ deceptus,
n. sp.” two have them 10-jointed, and I am almost certain
that the two $$ with 11-jointed antennae (the Types of
nilens, W. F. Kirby, and bella, Rohwer) on which Kirby
founded his “new genus” Euryopsis, are really the
unidentified $$ of two Eurys spp. of which 99 only have
been described—probably of laetus, Westw., and nitidus,
W. F. Kirby respectively. I venture therefore to sink
the name Huryopsis as a synonym of the earlier Burys.
(The so-called ‘“ Hurys”’ inconspicua, W. F. Kirby, 1s,
in my opinion, a Clarissa.)
[For Synopsis of the species see p. 294. |
— In the fore-wing the apex of the simply acuminate radial cell
is close to the margin of the wing, with at most a very narrow
(linear) space, but no real appendicular * cell,” separating it
from) thedatters .s) 1191 SW ae Seok wey toh chee ao me pce
18. Legs (especially the hind coxae and tarsi) very slender and
elongate, the tarsi evidently longer than the tibiae. Antennae
also long and slender, almost filiform as a whole, most of
their joints considerably longer than broad. According to
Mr. Rohwer the antennae should be 14-jointed, but in speci-
mens examined by me in B.M. Coll. the number of joints
varies from 12 to 15.
Generally the coloration of the body is thoroughly metallic,
muchas in Hurys. But in the 29 of one species the abdomen
beneath is testaceous.
18. Nrorurys, Rohw.
| For Synopsis of the species see p. 297. ]
— Legs and also antennae somewhat shorter and stouter than in
Neoeurys. The antennae can hardly be called filiform ;
they are rather moniliate, and the intermediate joints are
only a little longer than broad. The tarsi seem never to be
longer than the tibiae, in most cases they are evidently shorter.
The general coloration of the four species seen by me is not
metallic, but testaceous and black, except in atrata, which is
black with white markings. The number of joints in the
antennae varies extremely—from 9 in inconspicua to 14 in
thoracica. Of divergens I have seen specimens with 10, 11,
12, and 13 joints (all from Queensland). The most usual
number of joints in this species (and also in atrata) seems to
be ll’. « 4.22. #593) 2 SOS Grama Wh: Barby.
[For Synopsis of the species see p. 299. ]
Rev. KF. D. Morice’s Noles on Australian Sawflies. 259
INDEX OF GENERA TABULATED.
(Imported genera in italics. )
See | See
pages. pages.
= Ophrynopus) =. 27) a.es2bl | LI Philomastix <° : +256; 287
5) Were! ees, 20s ||) T2ePergula.” 4.9. 256,288
3. Xiphydria . . . « 253 | 13. Pterygophorus . 256, 289
4. Zenarge Pee 204 eel aa Oalvoa sae). ne. os Q5T
5. Trichorhachus ZA 2OOn | LOmeolyclonuss, Gaiety. 257
GaAnitarcidina a-ha e240) 16. Diphamorphos 257, 294
do Rerga 2) 5 ©. -.. 20d; 265 | 17. Hurys 257, 294
8. Xyloperga . . 255,265 | 18. Neoeurys 253, 297
9. Phylacteophaga . . . 255 | 19. Clarissa 258, 299
10. Cerealees . . . 255, 287 |
TRICHORHACHUS, W. F. KIRBY.
SYNOPSIS OF THE SPECIES.
All Trichorhachus species, except nitidus of which B.M.
possesses one ¢ and one 9, were described from single ¢
specimens, and any tabulation of their characters based
on such inadequate material can only be quite provisional,
since it is impossible to be certain which of these characters
are really specific and constant, and which hable to varia-
tion or even merely individual. The Type of one (australis,
Westw., described as a Schizocera) is at Oxford, all the others
are in B.M., and all this material, such as it is, I have
examined and compared with the original descriptions.
But I have seen no other representatives of the genus,
nor—so far as I know—has any one else !
Konow’s treatment of Trichorhachus in his Genera
Insectorum illustrates the danger of speculating on the
affinities of a genus without having seen any representative
of it. (It is only fair to say that in this case he expressly
acknowledges himself unacquainted with the insects
otherwise than in literature; but there are cases in which
he has unfortunately been less explicit.) He begins by
placing it in his division * Argides,” which he separates
from his “ Schizocerides”’ as having an intercostal nerve
in the fore-wing. But in fact such a nerve is not present
in any specimen of Trichorhachus. Yet neither can it
belong to the Schizocerides as defined by Konow, since its
260 Rev. F. D. Morice’s Notes on Australian Sawflies.
posterior tibiae are always spined before their apices.
Again he separates it from the genera with “ contracted ’’
humeral areas (= lanceolate cells) as having this area
* petiolated.” Really, however, it is not petiolated (though
Kirby so describes it), but contracted. Tvrichorhachus 1s
therefore a link between Konow’s Argides and Schizocerides,
and either the division between these must be given up,
or the definition of one of them must be emended, or a
distinct group, Trichorhachides, must be established one of
whose distinguishing characters will be the peculiar neura-
tion of the hind- -wing (see the Synopsis of Genera given
above, p. 254). Of ‘these alternatives I should myself
prefer the first, for the division of the Arginae into Argides
and Schizocerides seems to me to bring together genera
whose affinities are very remote, and to separate “others
which are probably very near relations. Such is almost
sure, I believe, to be the result when very large groups are
established on their agreement ina single arbitrarily selected
character. In this particular case of the Arginae, which
are perhaps the most widely distributed of all Sawflies,
and which appear to have reached all parts of the world,
and branched out here and there into new groups which are
quite unrepresented elsewhere, [ cannot think that any
classification of their genera is likely to be natural which
ignores their geographical distribution entirely.
As I only know one Trichorhachus 9 (viz. nitidus, Kirby),
and this seems to differ from its 3 in nothing but the usual
sexual characters (simple antennae, etc.), it must suffice
here to tabulate such differences as I notice in the 33,
and it must always be remembered that some of these
differences may not really be specific.
Ie Antennae’ yblack’ 44S! Di 7 ws mest yest utes Bee eee ke
— Antennae yellowish . . . Sica: “Aire ges! Ate Somme
2. Wings with clear bases but Aouad apices. Body above and
below bright metallic blue, only the labrum, tempora, and
extreme apex of abdomen yellow. Hind-legs entirely black.
australis, Westwood.
Type at Oxford. “ West AUSTRALIA.”
— Wings clear throughout. Body above nearly dead-black, but
slightly nigro-aeneous on parts of the thorax, and extreme
apices of abdominal segments a little discoloured. Labrum
yellow, but the rest of the face quite black, though Kirby
Rev. F. D. Morice’s Noles on Australian Sawflies. 261
describes it as yellowish. Abdomen rufescent beneath. |
Hind tibiae and tarsi yellow, except the apices of the former,
which are black. . .: . . . abdominalis, W. F. Kirby.
Typein B.M. “ West AustTRALIA, Swan River.”
3. Legs, including the femora, pale yellow. This is apparently
the smallest of the species
about 55 mm. long.
nitidus, W. F. Kirby.
Type in B.M. “ West AustRatia, Swan River.”
— Larger forms—about 8 mm. long. At least the femora of all the
legs are black or fuscous. . Te wth Wu ha as
4. Four posterior legs uniformly dark ecco: Face, tempora,
hypopygium with the genitalia, etc., and the front tibiae and
tarsi yellowish, the rest of the body metallic (chalybeous)
with reflections varying in different lights between blue-green,
indigo, etc. Wingsclear . . . hyalinus, W. F. Kirby.
Type in B.M. “ West Austratia, Swan River.
— Hind tibiae paler beneath than above. Otherwise quite like
hyalinus, except that the wings appear to be somewhat
GaGRer ae auc wee) cg re.) ss fe, VSOUTTMUS, Wo... Kinby.
Typen B.M. “ AustrRatia?”
The localities given above are cited from Kirby's List.
It would seem from them that the genus is hkely to be
confined to a single locality (Swan River): but if so, and
if the above are all really distinct species, it Is hard to see
why they should all be represented by “unica.” (Of course
more material may exist, though apparently unrecorded,
in Australian museums; in which case it is very desirable
that some competent local entomologist should revise the
genus properly.)
PERGA, LEACH (AND XYLOPERGA, SHIPP).
SYNOPSIS OF THE SPECIES.
Perga differs from any Northern genus in many significant
respects, €.g.—
Its larva (Pl. XV, Fig. 17) has no ventral prolegs,
while in all true ““ Cimbicides ”’ and ‘‘ Abiides ’’ of Konow’s
262 Rev. F. D. Morice’s Notes on Australian Sawflies.
classification these are present to the number of 16! This
fact has long been known, and the larvae of various Perga
spp. have been repeatedly described and figured.* It is
therefore rather surprismg to find Konow on page 41 of
his unfinished Monograph (Zettsch. f. Hym. uw. Dipt., Vol. I,
P., 169); tabulating six species of Perga as aerate larvae
“with 22 legs”! Myphotograph above cited is from
one of a number of specimens (preserved in spirit) in B.M.,
and it will be seen that the character is unmistakable.
Konow, I must suppose, had never seen one; but, having
made up his mind that Perga belonged to his Subfamily
Cimbicini, arrived by deduction from this premiss at the
conclusion that its larva must have 22 legs !
2. Its posterior tibiae have “ ante-apical spines ’’—a
character absent not only in all Cimbicides and Abiides,
but in all Palaearctic and Nearctic genera of Konow’s
Tenthredinidae except certain genera of the Arginz.
3. The structure of its thorax differs obviously in the
apical lobation of the scutellum, and also in certain other
less conspicuous details. (I do not here dwell on the
latter characters, as they are somewhat “ critical,’ and
have been dealt with by Mr. Rohwer in his recent classifica-
tion of the Suborder in Proc. Ent. Soc. Washington, 1911.)
4. The neuration is wholly different, Perga has in the
fore-wing (a) an undivided radial cell, (6) normally at least —
four cubital cells, (c) no lanceolate cell—the “ humerus ”
being obsolete or undeveloped, and in the hind-wing (d) one
cell only (a cubital).
All these characters (in some of which it agrees with all
other Australian and some 8. American genera) separate it
absolutely from all true Cumbicides and Abides, and quite
outweigh any reason for uniting it with them which might
be eee by the form of its vantennae !
Ae ain, a normal Perga has a reduced number of joints
in ie labial and maxillary palpi, namely, 3 and 4 re-
spectively, instead of 4 and 6, which latter is the number
in all Cumbicides and Abiides, and, so far as is certainly
known, in all Northern Tenthredinidae whatever ! (Xylo-
perga, however, does not possess this peculiarity, but has
4 labial and 6 maxillary palpi (PI. XII, Fig. 14) as in the
Holarctic genera.) But it is not certain what inferences
* Cf. Scott’s description and figures in Proc. Zool. Soc., 1859,
211, and Pl. LXII; also those of Davis in eC Clete, Vol. Il?
4 89, and of Froggatt i in Australian Insects, p. 72:and Pl. X, ete.
Rev. F. D. Morice’s Notes on Australian Sawflies. 263
ought to be drawn from this fact, so I here content myself
with merely mentioning it.
This difference in ate number of its palpi, combined
with other characters which shall presently be noticed,
certainly justifies the treatment of Xyloperga, as a good
subgenus, and possibly as a good genus, though at present
T am not convinced that it is either necessary or desirable
to exclude it absolutely from Perga. Certainly some species
of the latter (e.g. the bella group) seem to me to have really
more characters in common with Xyloperga, than with
others (e.g. dorsalis, ete.) in whose company such an arrange-
ment would leave them. Therefore, in separating Per, ga
and Xyloperga in my Synopsis of the Genera above, I have
rather deferred to what I believe to be the opinion of more
competent judges of such questions, than followed any
conviction of my own. But, as to the other “ segregations ’
which have been proposed mostly on single characters
often insignificant, and sometimes quite imaginary ,*
such as the presence or absence of a distinct Ist cubital
nerve in the wings of certain species, I must claim liberty
to disregard them altogether, till the collection of more
material makes it possible to say for certain, whether or
no these characters (when they exist at all) are really
characteristic of any natural groups of species. So far as
I have been able to test them, I have always found them
either “ individual,” or absolutely non-existent !_ So long
as, a majority of the species are known only from single
specimens, and the total number of supposed species is
no larger than at present, I can see no advantage whatever,
and on the contrary considerable disadvantage, in pre-
maturely establishing and naming sections, which may or
may not correspond to real natural groups. On this kind
of work I venture to think that “ the last word ” was said
* B.g. Leach says that P. polita has only 3 cubital cells. This
is not really the case in his own Typical specimen, the Ist cubital
nerve being merely interrupted in the middle, but not absent;
and examination of other specimens shows that the aberration is
not specific, but individual. However, on the strength of Leach’s
mistaken statement, Ashmead made polita, Leach, the Type of a
“new genus,” which he characterised by the absence of the Ist’
cubital nerve, and named “ Pseudoperga.” Perhaps, fortunately,
the same name had been already employed by Guérin (1845) and
Shipp (1894) to denote a different section of the genus, the Type
of which is lewisii, Westw.; so that Pseudoperga, Ashmead, may
safely be ignored as a homonym.
TRANS. ENT. SOC. LOND. 1918.—PaRTSII,IV. (MAR. 19)
264 Rev. F. D. Morice’s Noles on Australian Sawflies.
long ago by Aristotle's master Plato. He compares it to
the methods of an unskilful. butcher (%ax0S [MayELOOG),
cutting up his carcasses without regard to their “ natural
articulations ” (Go0o0a Fi méqvxe), and therefore not inserting
his knife between the meeting-points of the limbs, but
hacking through the bones themselves. This, I venture
to think, exactly describes the manner in which Leach’s
genus has been dealt with by such writers as Shipp and
Ashmead—of whom the former was evidently incompetent
to deal with it at all, and the latter, though versed in the
literature of the subject, seems to have had no actual
acquaintance with any of the species, whose affinities he
took upon himself to determine.
Xyloperga, Shipp, however (= Heptacola, Konow), 1s
at any rate a real group, and differs from normal Perga,
not only in its mouth-parts, and the other characters
mentioned infra in my Table, but in sundry other details
such as a peculiarity in the form of its clypeus, which is
rather difficult to describe but easy to recognise when once
thoroughly realised. It is (approximately) bisected trans-
versely into two distinct areas, a basal and an apical, the
latter being occupied (except at its extreme apical margin,
which is a little recurved) by a sort of shallow sulcus above
which the basal area rises somewhat abruptly to a higher
level. The division between these higher and lower levels
is nearly a straight line, so that the clypeus appears to
have a double apical margin, or, in other words, to end
before its real apex. Something of the kind occurs also
in one group of Perga (bella, ete.), in which and also
in certain spp. of " Heptacola * * G.e. Xyloperga) Konow
describes the phenomenon as ~ Clypeus in der Mitte quer
gebrochen,”’ but he does not utilise it as a general character-
istic of the latter genus.
The scutellum, also, of Xyloperga (as pointed out by
Konow) is somewhat more narrowed posteriorly than in
normal Perga spp. (subtriangular rather than oval or
subquadrate), and this generally brings the “ apical lobes ”
rather nearer together than in the other case.
Unfortunately most of the forms which make up Xylo-
perga are represented by at most one or two specimens in
B.M. and at Oxford. The only species of which I have
seen anything like a series is wnivittata, W. F. Kirby, which
Konow, gue wrongly, sinks as the g of “ newmanni,”
Westw. ( = ferruginea, Leach). Konow is also mistaken
Rev. F. D. Morice’s Notes on Australian Sawflies. 265
in commencing his List of “* Heptacola”’ spp. with H.
macleayr, Westw.; for the latter, as I have mentioned
elsewhere, is neither a Heptacola, nov a Perga, but identical
with Froggatt’s Type-species of Philomastix, hitherto
known as glabra, Froggatt. It must be known in future
as Philomastix macleayi, Westw.
SYNOPSIS OF PERGA (AND X YLOPERGA) SPP.
OO
fe
1. Fore-wing with its third cubital nerve (Pl. XV, Fig. 14) rising
at first perpendicularly from the cubitus, but soon becoming
curved (or even suddenly angled) inwards and running ob-
liquely towards the stigma. It is therefore not nearly parallel
tom the second scubitalomenyen, 20 sa eety. Wes 58d:
— Fore-wing with its third cubital nerve (Pl. XV, Fig. 15) approxim-
ately straight throughout, and parallel (or nearly so) to the
SECONG CUDIbAlMERVG sou to hi crn, 160) dee ayia 1S, 4 2%
2. Antennae short, but not paradoxically so *—generally about
* Two species, both belonging to the section of Perga in which
the third cubital nerve is sharply bent inwards, cannot at present
be tabulated by their antennal characters, since the unique Type-
specimen of each had lost its antennae before the species was
described and figured. These are P. walkerii, Westwood, and P.
christii, Westwood (Types of both at Oxford). I will therefore here
mention other characters by which they may probably be recognised
if they should be rediscovered.
|. P. walkerii is a rather large and robust form about 18 mm.
long. The head (above), the pronotum, and the greater part of the
legs (except the black hind femora), are fulvous. The whole
mesonotum including the scutellum (!), the metanotum, the three
basal segments of the abdomen above and all its ventral surface up
to the sawsheath are black. The remaining (apical) segments of
the abdomen above are reddish-fulvous. The wings are stained with
yellow, their venation and the stigma brown. (Details of SSoWee
Pl.. XIV, Fig. 12.)
2. P. christii has the abdomen entirely chalybeous. The head
and thorax are blackish with very copious whitish markings. Of the
latter colour are the clypeus, labrum, orbits of eyes, antennal
tubercles, two spots on the vertex, the edges of the pronotum widely,
a spot in the posterior corner of the middle mesonotal lobe, the whole
scutellum with its apical lobe-like processes and the ridges which run
obliquely from its basal corners towards the insertions of the wings.
The basal half of each fore-wing is clear and colourless, but its apical
half is distinctly infuscated throughout and especially so under
the stigma. The veins and stigma are black. Length about
15 mm.
Konow treats this sp. as a synonym of foersteri, West. (1. e. bella,
266 Rev. F. D. Morice’s Notes on Australian Sawflies.
as long as the distance between the compound eyes. Their
3rd, 4th and 5th joints are all longer than broad, distinctly
separated from each other and from the apical joint, which
forms a “‘ club” by itself. The antennae are thus “ capitate,”
and not simply “clavate” . .. Fie HABER bo
— Antennae paradoxically short—about as loke as the distance
between their insertions. Some at least of the intermediate
joints are broader than long, and as well as the apical joint
they form part of the “club,” which therefore commences
immediately after the two short basal joints (cf. Pl. XV,
igs 1S): & esaeg ee ee) cee ee ayer, Ga Pe WOE
3. The hind tarsi (including the claw Cone) are eo medentn shorter
than: the hind tibiae: ).9))-9 0-1 22 ve ern aa
— The hind tarsi are approximately equal in ieneth to the hind
tibiae. (Group of lewisii and jferruginea. For details of
the ‘“‘ saws ”’ in this group, see Pl. XIV, Figs. 13, 14, 15.) 20.
4. Neither antennae nor scutellum ever black, but yellowish or
brownish. (Saws asin Pl. XIV, Figs. 1to10.) . . . 5.
— Either antennae or scutellum (or both) are black. (Saws as in
PIX DVe tics. (Osan etl) genes Bee a mL AS
5. Scutellum bisected by a wide and deep longitudinal furrow.
— Scutellum at most divided by a fine line or an inconspicuous
depression, or not divided at all. . . . . . . . 6.
6. The head above, the mesonotum (except its scutellum) and
almost the whole abdomen above concolorous—metallic
green or blue (*‘aeneous”’ or “ chalybeous”’). Fore-wings
stained throughout with yellow. Middle of scutellum smooth
AG InpuUnctatens 8 ec. \as nies ur) ait ss ta eee he
— The head, the mesonotum (or at least its middle lobe), and
usually the abdomen not aeneous nor chalybeous, but yellowish
or brown (rarely with obscure violaceous reflections in certain
lights). Wings in some species quite clear (‘ hyaline”),
in others slightly clouded in parts, but seldom, if ever, really
Vellow> =i. 5. Weer eee ok ae a Ee aan ee BT
7. Mesopleura entirely pale, concolorous with the pronotum and
scutellum. Abdomen more or less discoloured (beneath and
Newman), but this is certainly a mistake, for the latter species be-
longs to the division of Perga in which the third cubital nerve is
straight, whereas in christit this nerve is very strongly bent, even
angled !
I am inclined to think that the species to which christii comes
nearest is dahlbomii, Westwood, but it is impossible to be sure
without having seen its antennae. Those of dah/bomii are extremely
short (Section “LL of Kir by’s List).
Rev. F. D. Morice’s Notes on Australian Sawflies. 267
at the sides) in some specimens, but this may be due to im-
maturity. Ido not believe that this is more than an aberra-
tion of the next species (dorsalis). It agrees with it exactly
in all structural characters, details of ‘‘ saws,’ ete. Nor
can it be considered as a “subspecies” (== local race) since
both forms occur in the same locality. affinis, W. F. Kirby.
Victorta.. Type in B.M.
Mesopleura at least partly, and abdomen entirely in all specimens
seen by me, chalybeous or aeneous (concolorous with the
mesonotum,theadsete,). «ue ae alse < sP ek A 8,
8. Large form (about 24 mm. long). The general ground-colour
in all specimens seen by me is rather green than blue. The
details of the “saw” (Pl. XIV, Fig. 1) differ from those in
all other spp. except affinis. This was the first species of
Perga to be described, and is the Type of the genus.
dorsalis, Leach (? = eucalypti, Scott).
N.S. Wates and Victoria. Type (a g) in B.M.
— Very like dorsalis but smaller (about 20 mm. long) and with a
very different saw (Pl. XIV, Fig. 7). One specimen in B.M.
is coloured like dorsalis, but the others are all rather blue
GHAR OTECM ay het sok 2.8 oe ONTICON Satan.
There are three examples of this form in B.M., two from
Queensland and one from Adelaide, all 92. At Oxford
there is only one, also a 9, from Adelaide, which Westwood
—wrongly, I believe (v. imfra)—considered to be the 2
of his schiddter 3, though it is quite unlike the latter in
coloration. It appears therefore necessary to give it a
new name.
QUEENSLAND and ADELAIDE. Type in B.M.
9. Mesonotum with its side-lobes chalybeous. The middle lobe,
head, and part of the abdomen testaceous.
schiddtei, Westw.
This I believe to be the true 9 of schiédtei, Westw. It
strongly resembles the 3 in coloration and other char-
acters. In B.M. there are, besides the unique 9 specimen
(S. W. Australia, Swan River), three g¢ exactly like
Westwood’s Type, and all, like the 9, from 8. W. Australia
(one from Swan River). There is no similar 9 at Oxford,
and Westwood probably was unacquainted with it.
268 Rev. F. D. Morice’s Notes on Australian Sawflies.
S. W. Ausrratia (Swan River, etc.). Type (a 3)
Oxford.
— All lobes of the mesonotum entirely testaceous, or rarely brown
(mo part: chalybeous): 5... . Fs. J. = eeelO:
10. Scutellum quite smooth and impunctate with no Er roerioe of
a dividing line or furrow. Wings, at least towards their
apices, slightly infuscated oye « « ~~. thlugu, Westw.
S. W. Austraria (Swan River). Type at Oxford.
— Scutellum punctured, or bisected by a longitudinal line or a
shallow furrow. Wings glassy and quite clear. . . . II.
11. Scutellum with dense rugose punctures, bisected by a distinct
though shallow longitudinal impression . . kirbii, Leach.
Victoria. Type (a 3) in B.M., also one 9.
— Punctures of scutellum more or less remote. . . . . 12.
12. Scutellum with a very few hardly noticeable punctures, bi-
sected longitudinally by a fine impressed line.
brevitarsis, n. n
The unique specimen in B.M. was referred by W. F. Kirby
to hirbir, but is evidently not that species. It differs
from all other forms by its extremely short tarsi, which
look only about half as long as the tibiae !
S. W. Ausrratia (Swan River). Type in B.M.
— Scutellum more largely and closely punctured than in brevi-
tarsis, but not coarsely and rugosely as in true kirbii. Hind
tarsi of normal lengthh . . . . . . agnata,n. sp.*
This also is a unique specimen. Its saw (Pl. XIV, Fig. 3)
is more like that of dorsalis than those of the species to
which it seems more nearly allied. Towards its base,
however, which is not shown in the Figure, the teeth alter
their shape and become bent as in klugii, ete. (Possibly
this character is merely individual. More specimens are
needed to settle the point.)
Vicrorta. Type in B.M.
* Perga agnata, n. sp.
2 P. kirbii, Leach, notis paene omnibus—scilicet statura, colore
lutescente, alis limpidis, ete.—simillima.
Differt scutello sparsius punctato, lobis eiusdem apicalibus minus
productis, denique terebrae denticulis aliter formatis—scilicet
haud uncinatis omnibus, sed plerisque (ut in P. dorsali et affini)
lenissime tantum curvatis, immo paene rectis.
3 differt a P kirbii 3 scutello multo sparsius punctato.
Rey. F. D. Morice’s Notes on Australian Sawflies. 269
13. (5) General colour yellowish-brown * with certain areas paler
(clear light yellow) especially the scutellum, the posterior
corner of the middle mesonotal lobe, and a series of marks
on the sides of the abdomen (where the lateral margins of
the dorsal plates fold over and become ventral in situation).
Hind femora widely blackened, tibiae so only at extreme
apex. Wings yellowish, but otherwise almost clear. The
longitudinal furrow on the scutellum is very noticeable, linear
at its base and growing wider and deeper as it approaches
the apex, but its lateral limits are not sharply defined. (The
absence mentioned by Leach of a Ist cubital nerve is not a
constant character, though Ashmead has treated it as generic !
Even in Leach’s own Type the nerve is not really absent in
either wing, and in most specimens it is quite normally
develapedaje sets" F) toca oa A ee. olata) Leach:
EASTERN AustRALiA (from Victoria to Cairns in Queens-
land). Type, and many other specimens in B.M.
— Very like polita but darker than normal specimens, and the
scutellum is not vellow but brown like the areas adjacent
to it. . Hind femora and tibiae concolorous, pale throughout
in all specimens examined. Lateral marks on abdomen
much as in polita. Wings distinctly and even strongly
infuscated under the stigma. The furrow on the scutellum
seems distinguishable from that in polita by its more sharply
defined diverging margins. . . . castanea, W. F. Kirby.
Kirby described what I take to be certainly the ¢ of
this species under the name divaricata, but associated
with it a 2 belonging to quite another group, namely a
bella. (Vide infra, 31, “and cf. Pl. XV, Fig. 6, with Pl. XIV.
Miowd andy Pl eV, Kies ..5;. 73.9.)
serosa: Type in B. M.
14. (4) Abdomen black with no part red, but segments 7 and 8
(above) each with a broad apical band of pale yellow, that
on segment 7 deeply excised anteriorly (almost interrupted).
The 5 preceding segments are quite black above, but streaked
with yellow on the sides and venter. Scutellum yellow, but
* The dorsum in Leach’s Type-specimen is darker than usual,
and shows obscure metallic reflections (violaceous). Probably
this results from the great age of the specimen. It must have been
in the Museum for more than a century.
270 Rev. F. D. Morice’s Notes on Australian Sawflies.
labrum and antennae entirely black. Length about 15 mm.
Saw;Pl: XIV Big 16. iy. 2 =. 2+ 4, anhopa,m: sp.*
S. W. Ausrratta (Yallingup and Kalamunda). Type
(and other specimens of both sexes) in B.M.
— Abdomen belted with red, black at base and apex, and without
any yellow markings. Scutellum margined with yellow.
Head above black. Hind tibiae and tarsi dark red (not
“entirely black” as stated by Konow). Wings dusky,
blackish brown, especially under the stigma. Length about
14mm. Saw, Pl. XIV, Fig. 11 . . . esenbeckit, Westw.
S. W. Avusrratia (Swan River). Type at Oxford.
Another 2 in B.M. :
15. Antennae with only five ¢ joints visible. Wings in West-
*Perga antiopa, n. sp.
© Nigra, labro antennisque concoloribus. Lutea vel eburnea
sunt—tubercula antennalia, parsque genarum his adjacens; clypei
latera; mandibularum maculae basales; striga longa (superne
abbreviata) postocularis; pronoti margo posterior; scutellum ; pleu-
rorum pedumque major pars (apicibus vero tibiarum posticarum
tarsorumque nigris); segmentorum abdominis dorsalium 7™ et
8% margines apicales; et in segmentis praecedentibus maculae
magnae laterales ventralesque, quae tamen desuper spectanti vix
(aut ne vix quidem) apparent.
Scutellum sparse punctatum, sulco mediano divisum. Alae
brunneo subfuscatae. Clypei apex subexcisus. Antennae capi-
tatae, normales, articulo 3%° sequentibus ducbus conjunctis
subaequali.
3 Pictura corporis cum @ satis bene congruit; differt vero capite
et thorace plus minusve copiose rufo-variegatis, etiamque antennis
post articulum 2%", pedibus totis, mesonoto pleurisque partim
rufis, clypeo et plerumque labro immaculatis, flavis, ventre copiosius
flavo-picto.
+ Konow questions this, but Westwood’s statement is perfectly
correct, and his enlarged figure of the antenna shows the character
clearly, (Cf. also my Fig. 18, in Pl. XV which is drawn from Kirby's
Type-specimen of bisecta.)
Authors have blundered strangely about this species. W._F.
Kirby placed his bisecta in his Section I, as though its antennae had
been of normal length and shape, while he actually enumerates
mayrii among the species of his Section IIT, as though its antennae
were seven-jointed !_ Shipp makes confusion even worse confounded.
Although Westwood’s Type was actually in his charge, and he
might have counted for himself the joints of its antennae and the
nerves of its cubital area, he adopts, instead, Kirby’s erroneous
classification and Westwood’s figure of the wing in which the
neuration is imperfectly represented, and erects accordingly an
imaginary “ genus ’—of which he names mayrii, Westw., as_ the
Rev. F. D. Morice’s Notes on Australian Sawflies. 271
wood’s Type-specimen with the Ist cubital nerve very faint,
nearly obliterated (“*fere obliterata,” as the author correctly
states), but not quite so, though his Figure does not show it
at all. (In Kirby’s Type of bisecta this nerve is quite distinct
and normal!) The body is almost entirely fulvous, but
with the pleura, sterna, metanotum, propodeum, hind fe-
mora, a spot and streak on the middle mosonotal lobe, and
the edges of the scutellum as well as a large mark on its disc,
more or less completely blackened. The wings have a yellow
stain, and their neuration and the stigma are brownish. A
larger and more robust species than most of this group
(Section IL in Kirby’s List)—about 18 mm. long. I have
not been able to examine the saw, and cannot describe its
characters. . . . mayrii, Westw. = bisecta W. F. Kirby.
I have carefully compared the Types of mayrii, Westw.,
and bisecta, Kirby, and am certain that the two belong to
one species. Both specimens were taken by the same
collector (Mr. Du Boulay) in West Australia; mayriv at
Swan River, bisecta at Nicol Bay.
W. Ausrraita, Type of mayrii at Oxford. Type of
bisecta in B.M.
SANTO Ae, Wath EI JOINtSy) 2° ath tuhe resets 31, See eto! 1 Gs
16. Thorax nearly unicolorous, lighter or darker testaceous
throughout . . . peti tin 2p. rn, Magy (dll cache ral be
— Thorax black with yellow inenleinee Bes cape iia Iu) eaety SIGs
17. General colour pale testaceous. Head and mesonotum opaque,
very closely punctured and rugulose. Hind tarsi pale.
belinda, W. F Kirby.
The details of the saw in this species curiously resemble
those which appear elsewhere only in the group of bella.
Of. Pl. XIV, Fig. 17, and Pl. XV, Figs. 5, 6, 7 and 9. But
its other characters, and especially the nee of the 3rd
cubital cell, suggest that it can only be very remotely
connected with that group.
S. Austra. (Adelaide). eos in B. M.
type—characterised by seven- Pomel antennae Re only ise
cubital cells !! It seems to me altogether unreasonable that,
when a so-called “genus” is thus founded solely on blunders and
misrepresentations, and corresponds to no real group of natural
objects whatever, it should be allowed ‘ standing in nomenclature ”
merely because the author has gone through the form of * * selecting
a type.” Such work is certainly no contribution to science, and
does not deserve to be treated seriously as literature.
272 Rev. F. D. Morice’s Notes on Australian Sawflies.
a ruddy brown. Head and
—- General colour much darker
mesonotum shining; the punctures on the latter large, but
very sparse. Hind tarsi blackish. . . . lucida, Rohwer.
The Type is unique, and I have been unable to examine
the details of its saw properly, but what I can see of them
reminds me of the lewis2? group, and especially of ferru-
ginea, which it resembles also in coloration, though its
sculpture-characters are very different.
N.S. Wates. Type in B.M.
18. Dorsum of abdomen red, except at the base and apex which
are black. Head and thorax black with copious yellow
markings (two large spots behind the ocelli, another in the
posterior corner of the middle mesonotal lobe, ete.). Length
about 16 mm. Wings quite clear. . . cressonii, Westw.
Perhaps, as Konow thought, this is the Q of brullei,
Westw. But its femora are black, which is not the case
in brullec 3, and this is a character in which the two sexes
of a Perga-species generally agree.
ADELAIDE. Type at Oxford.
— Dorsum of abdomen entirely, or at least throughout its longi-
tudinal diameter, dark violaceous or chalybeous. . . 19.
19. Clypeus, labrum, apices of hind tibiae and tarsi, and also—
teste Westwood *—the antennae, black. Abdomen nigro-
violaceous. Wings not distinctly infuscated. Scutellum
* T have only seen one © certainly referable to dahlbomii, Westw.,
namely the original author’s Type-specimen, and this, as well as
the jg which he described with it, has now lost both its antennae.
I'wo 3, however, in B.M. agree precisely with Westwood’s 3 in
other characters, and both these have black (or at least blackish)
antennae. Neither these ¢3, nor either of Westwood’s specimens,
are stated to have come from any particular district in Australia.
Two 9° in B.M. were supposed by W. F. Kirby to belong to the
same species, but they differ greatly in coloration from the type,
having the antennae, clypeus, labrum, and the whole of the tibiae
and tarsi yellow. (\lso in one of them the sides of the abdomen
are broadly rufescent.). On the. whole they agree better with
christii, Westwood, and come from the same locality, viz. Swan
tiver. But they differ from Westwood’s Type of christii in several
characters— having, ¢.g. entirely clear and colourless wings, no
yellow streaks between the insertions of the wings and the basal
corners of the scutellum, the apical lobes of the tatter not vellow,
as in typical christii, but black, and the abdomen rather violaceous
than cyaneous. On the whole I can only think them to be neither
dahlbomii nor christii, but a distinct species of the same group
from which I propose the name vacillans.
Rey. F. D. Morice’s Noles on Australian Sawflies. 273
flatter than usual, without the usual distinctly projecting
apical lobes, but with its whole extreme apical margin slightly
raised, and ending on either side in a sort of obtuse angle
only—not an actual protuberance . . dahlbomii, Westw.
Precise habitat not recorded. Type (Q) and Co-type (3)
at Oxford.
— Clypeus, labrum, apices of hind tibiae, and tarsi not black but
yellow, as are also the antennae. Abdomen cyaneous.
Fore-wings with the bases clear but the apical half distinctly
clouded especially below the stigma. Scutellum with normal
(yellow) apical lobes, an oblique narrow yellow streak runs
from each of its basal corners towards the tegulae.
christii, Westwood.
W. AusrraLia (Swan River). Type at Oxford.
20. (3) Antennae black. Length only about 14 mm. Otherwise
hardly to be distinguished from the species next following
(lewisii). Both are almost entirely brownish-yellow above.
the head and thorax rugosely sculptured and dull, the abdo-
men smooth and somewhat shining, the apices of the hind
tibiae and tarsi black. In both the eclypeus is rather dull,
and scattered over it are rounded pits or “ foveae,” each
containing at its bottom a puncture from which proceeds a
longish hair, . . . guerinii, Westw. = smithii, Westw.
This 2 is called by Westwood smith, but I feel little
doubt that it is the 2 of the 3 which he had already de-
scribed under the name guerimi, and the latter name must
therefore be adopted.
Konow considered guerinit to be the 3 of lewisi (de-
scribed long before from a Q), and treated smithii as the
2 of ventralis 3 described by Guérin in 1845. But the
measurements given by their authors for ventralis 3 and
guerini $—the former being evidently the larger insect—
and also the agreement of guerini with smithis and not
with /ewis77 in the rather unusual character of entirely black
antennae, make me sure that Konow was mistaken, and
that he has reversed the facts. (At the same time there
seems to be at present no positive proof that the above gS
and 99—which differ altogether in colour—are really in
any way connected. That they are so, seems to be merely
an inference from their agreement in certain characters -
274 Rev. F. D. Morice’s Notes on Australian Sawflies.
which are not all of equal importance.* In both cases
the °° seem to be extremely common, while the $3 are
hardly known at all. It is most desirable that these
doubts should be cleared up by rearing larvae of both
forms on a large scale, which would be sure sooner or
later to procure the evidence that is wanted. (Kirby’s
“ sericea’”’ J in B.M. appears to me identical with guerinii
3 of Westwood, and I think it likely that “‘ chalybea”’ 3,
Froggatt, is either the same, or perhaps more probably
the true ventralis. Unfortunately Mr. Froggatt does not
mention the colour of the antennae in his species.)
The Types of guerinit (3) and smithii (Q) are both at
Oxford. Westwood gives no particular locality for either,
but specimens of smithi in B.M. are from Victoria.
— Antennae not black, but luteous or ferruginous. . . . 21.
21. Larger (about 19 mm. long) and paler. Yellowish with the
apices of hind tibiae and tarsi, and usually the sides of the
mesonotum blackened . . « lewisii, Westwood (1836).
TASMANIA and VICTORIA.
— Smaller and darker, brownish-testaceous, with legs and sides
of mesonotum concolorous. (P. froggatti (2), Rohwer, in my
opinion certainly belongs to this species, and ‘* newmanni,”
Westw., and * sellata,” Kirby, are 5 ¢ of the same insect.)
JSerruginea, Leach = froggatti, Rohwer.
N. 8. Waters and Vicroria. The Type of ferruginea,
Leach, according to Kirby, is a 2 in B.M. Westwood,
however, says that it is a g at Oxford; but he cannot
be right as to this, for Leach describes a 2 only, and says
distinctly Mas latet! The Types of Sfroggatti (2) and
sellata (3) are in B.M. That of newmanni 3 is at Oxford.
22. (1) Antennae with only 5 joints really separated from the
“club,” but the latter is sometimes constricted (on one side
only, not all round !) so that in certain aspects the antennae
look seven-jointed. A more important character is the
* The character of “three cubital cells only,’ on which Guérin
founded his Subgenus Pseudoperga for lewisii and ventralis, is
certainly not re liable. The first cubital nerve is not always absent
in any species of the group, and very seldom so in ferruginea, Leach,
which clearly belongs to it.
Rev. F. D. Morice’s Notes on Australian Sarwflies. 275
following—N.B. labial palpi scarcely thicker than the max-
illary and with only three joints, maxillary with only four,
(The same is the case with all the species tabulated
DOOVCr) Gee eertrsa se AD an ie 5 ae f 20%
— Antennae with 6 joints diecuctly Bseeentad thorn a club.
Labial palpi much thicker than the maxillary, and /owr-
jointed; maxillary palpi six-jointed (Genus, -or Subgenus ?,
Xyloperga, Shipp = Heptacola, Konow). In this _ latter
character the Group agrees with practically all non-Aus-
tralian Tenthredinidae except a few in Central and South
America ! Bs att ve ck, TM 9 ec) Mor
23. Antennae far longer thane in any other species; all their joints
before the club slender and elongate (joints 3 and 4 subequal,
5 a little longer, and more than half as long as the club).
All these joints and the base of the club are black, its
apex is white (Pl. XV, Fig. 20). Abdomen bright testaceous
above, whitish beneath, blackened on each side, these lateral
black vittae successively widening posteriorly and so spreading
more and more on to the dorsum, till on the penultimate
segments they actually meet.
cameronii, Westwood = leucomelas, Rohwer.
This is a very distinct and remarkable species. Un-
fortunately in Westwood’s Type-specimen the antennae
are wholly wanting and were so when he figured and
described it. But in the Type-specimen of lewcomelas,
Rohwer, which I have carefully compared with West-
wood’s Type of cameronii, and which, I feel sure, is con-
specific with it, the antennae are perfect, and at once
suffice to distinguish the species from any other. Cf.
Pl. XV, Fig. 20 (drawn from the Type of lewcomelas).
Type of cameronw at Oxford, of lewcomelas in B.M.
Westwood cites no particular locality for cameron. The
Type of lewcomelas is from QUEENSLAND (Cairns).
— Species with normal antennae, and very different coloration
CPO FCOMCTON UL ce als) Mins clei Wet @ ole os biome ape ad
24. All tibiae and tarsi quite black. Abdomen red and very shining.
Antennae and scutellum black. Fore-wings with a strong
brownish clouding below the stigma. Length about 14-15 mm.
Saw, Pl. XV, Fig. 4. ire ee glabra, W. F. Kirby.
QUEENSLAND (Mackay) and N. 8. Wates (Sydney).
Type in B.M.
276 Rey. F. D. Morice’s Notes on Australian Sawflies.
— All tibiae at least (usually the tarsi also) entirely pale, or black-
ened. only at them apices’. "22 2) {its Sa) or ees
25Antennser black. acl FW. (SiO aera et ae OPN ote Pees
— Antennae never black, but yellow or testaceous. . . - 27.
26. Scutellum pale, labrum and abdomen entirely black, saw (very
peculiar) Pl. XV, Fig. 10.. ... ._. ~. bditcolor, Leach.
Vicrorra and N.S. Waxes. Type in B.M.
— Scutellum black, labrum yellow, abdomen yellow at base and
MPOX. Lue woe fee ee ee ees ge Ue SS peNOlge: Wesbwe
Victoria. Type at Oxford.
27. Small species, about 13 mm. long. Hind tibiae blackened at
apex. Body almost entirely testaceous, except that the
pronotum is bordered with yellow. Westwood described
this 9 as a new species (viz. dalmanni), but I think Konow
is right in considering it to be the Q of /Jatreillec described
A
(from a ¢ only) by Leach.
latreillei, Leach = dalmanni, Westw.
ADELAIDE to SypNEy. Type of latreile: (3) m B.M.
Type of dalmanni (Q) at Oxford.
— Larger forms, about 17 mm. long or more. Hind tibiae pale at
MDER. 8. ey ee hae ee > Mii. Orn ke ae edn Ae ee
28. Abdomen without white or yellow lateral markings; it is
either testaceous entirely, or testaceous with the apex black,
above, beneath, and at the sides i ipey sy ates wh<derRebe
— Each side of the abdomen is ornamented with a continuous
series of uniform white or yellow marks. These are situated
on the lateral margins of the successive dorsal plates; but,
since the latter are folded inwards under the abdomen, the
marks to be fully seen must be viewed ventrally.* . . 30.
29. Hind femora broadly blackened, contrasting strongly with the
testaceous tibiae and tarsi. Thorax above, including the
pronotum and scutellum, almost entirely black, dull and
deeply punctured. Abdomen testaceous throughout. Fore-
wings with a strong yellow stain except at their margins which
are faintly violaceous in certain lights. Saw, Pl. XV, Fig. 8.
About 16mm.long . . . . : . . hartigti, Westw.
Type at Oxford.
*
Similar marks have been already mentioned as occurring in
some species of other groups (polita, antiopa, etc.).
Rev. F. D. Morice’s Notes on Australian Sawflies. 277
— Hind femora immaculate, testaceous, concolorous with the
tibiae and tarsi. Abdomen testaceous, black at the apex.
In size, habit, and most external characters, this species
much resembles hartigii, but its saw (Pl XV, Fig. 9) is
altogether different, and almost identical with that of bella.
gravenhorstii, Westw.
Type at Oxford,
30. Head, mesonotum (except its lateral areas which are sometimes
blackened), scutellum, and abdomen, testaceous with copious
yellow markings, e.g. a pair of spots behind the ocelli,
an elongate oval mark on the middle mesonotal lobe, a
series of marks (as in polita, antiopa, etc.) on the infolded
margins of the abdominal dorsal plates, ete. Saw, Pl. XV,
Big! ie) te We ok rer oe Meu Dela, Newman (1841)
= “divaricata” 2 (nec 3), W. F. Kirby (1893).
(The 2 associated by Kirby with his “ divaricata” 3
belongs in my opinion to this species. His g—which
is the Type—I have already identified as the male of
caslaned.)
Vicrorta; 8. AuSTRALIA (Adelaide).
— Yellow markings much as in bella, but the general colour of the
body is not testaceous, but very dark, black, or nigro-chaly-
beous, or nigro-violaceous .. : Reena) ele
. Hind femora black. Yellow marks af head Rone and abdomen
as in bella, but the ground-colour very different, that of the
thorax black, that of the abdomen above chalybeous. Scu-
tellum black, except its apical lobes and a triangular space
* The Type of bella seems to have long ago disappeared. It
was from Adelaide, “a single 2 in the cabinet of the Entomological
Club.” In 1844 the Club presented its collection to B.M. But
according to Kirby’s List (1882) the three specimens of bel/a from
Adelaide then (and still) in the Museum were all ~ purchased. oe
If so—and Kirby’s statement is borne out by the Museum “ Register
of Accessions ’——none of these can be the Type, which would Shave
been registered as. °° presented,” and not as “* purchased.” (F. Smith
seems to have confounded bella with /erruginea, and Westwood
states that the two forms are very near to each other. But I can
see no likeness whatever between them, and they certainly belong
to quite diffsrent groups, since they agree neither in neuration nor
saw-characters. )
278 Rev. F. D. Morice’s Notes on Australian Sawflies.
(stretching from these lobes to the base of the scutellum),
which are yellow fake: ->. e . bella, Vareen=s
N.S. Waues. Type in B. M.
— Femora tibiae and tarsi concolorous, testaceous. Middle lobe
of mesonotum not spotted in the middle with yellow, but
testaceous at its sides. Ground-colour of thorax and abdo-
men black, with a violaceous tinge in certain lights. Pale
markings of head and abdomen as in typical bella.
rubripes, Rohwer.
TasMANIA. Type in B.M.
32 (22) Dorsum of abdomen for the most part yellow or tes-
i \
taceous aa ee te Uae ete Pests Me AI bone (Oysh
— Dorsum of abdomen chal beous; at most its sides and ventral
surface are pale or red = a) 4 da) es ee OO
33. Antennae blackish. Body except the base of the abdomen
almost entirely yellow. Size appears to vary greatly—from
15 to 20 mm. long. Details of saw Pl. XV, Fig. 12.
aurulenta, n. spot
2 This specimen in the B.M. collection is labelled “ bella, var.
nigra, Rohw.” But I believe that this name is unpublished. It
is exceedingly like rubripes, and I doubt if it really differs from the
latter specifically. In fact, since all these forms agree absolutely
in practically everything but colour, and especially in the highly
characteristic structure of their saws, | am tempted to think that
Kirby, Westwood, etc., were right in including them all as forms
of bella.
The 3 of bella is probably, as suggested by Konow, /foersteri,
Westw. But if so, of course Newman’s much older name (bella)
should be adopted for the species. Konow also sinks the name
christii, Westw., as a synonym of ** foersteri,” i.e. bella. But this
is certainly a mistake, for christit (see above, 19) belongs to the
section of Perga in which the 3rd cubital nerve is bent (Pl. XV,
Fig. 14), while in “ /oersteri”’ and bella (2) this nerve is straight
(PIPEX Va tig.; 15).
+ Perga (Xyloperga) aurulenta, n. sp. 9.
Pallide flava paene tota, sed partibus his denigratis—antennis ;
suturis abbreviatis inter antennas.ocellosque posticos, suturis occipi-
talibus et macula prope occipitale foramen sita; fascia bilobata ante
pronoti marginem basalem, vitta lata triangulari in mesonoti lobo
medio, aliaque macula (multo minore) ante se sutellum ; fascia basali in
dorso abdominis; pedum posticorum femoribus, tibiarum apicibus,
et parte tarsorum. Clypei dimidium basale elevatum, et a dimidio
apicali concaviusculo truncatura fere rectilineari transversa separa-
tum. Scutellum apicem versus angustatum, lobis eitusdem apica-
libus satis longis. Alae flavescentes, venis et stigmate aurantiacis.
6 ignotus.
Rev. F. D. Morice’s Notes on Australian Sawflies. 279
I have seen two specimens only (both 99) of this very
distinct species, which were received at the B.M. in 191]
from Mr. H. J. Hillier. Except these, I have seen no
Sawflies at all from Central Australia; and thoueh evi-
dently congeneric with the Xyloperga spp. of the coast
districts (Swan River, etc.), they differ exceedingly from
them all in coloration, resembling rather in this respect
certain groups of Hymenoptera which are chiefly found in
the sandy deserts of tropical and subtropical Africa and Asia.
CeNnTRAL AusTRALIA (Hermannsbure). Type in B.M.
— Antennae not blackish, but ferruginous or yellow. . . . 34.
34. Apices of hind tibiae blackened. Head thorax abdomen and
legs for the most part nearly concolorous (ferruginous), but
the abdomen in some specimens is more or less clouded or
streaked transversely with black. Length about 15 mm.
Details of saw, Pl. XV, Fig. 13. . wnivittata, W. F. Kirby.
(The resemblance between this insect and “ newmanni,”
Westwood (i.e. ferruginea, Leach), of which Konow
supposed it to be the 9 is quite superficial. In all struc-
tural characters they wholly differ.)
QUEENSLAND (Mackay). Type and other specimens
($$ and 99) in B.M.
— Legs quite pale, not blackened at the apices of the hind tibiae.
Head above for the most part black. . . . . . 365.
35. Mesonotum with the middle lobe only anteriorly, and the side
lobes only posteriorly, blackened, otherwise concolorous with
the dull pale-brownish scutellum. Tempora and a streak
behind each of the posterior ocelli whitish yellow, otherwise
the head above is black. Length about 12} mm.
leachii, Westw.
Victoria. Type in B.M.
— Mesonotum quite black, scutellum clear yellow. A handsome,
highly-coloured insect. Larger (about 14 mm. long) than
leachii, though Westwood says it is smaller, evidently by a
mere slip, as he also gives correctly the measurements of
the two in lines. Details of saw, Pl. XV, Fig. 11.
halidaii, Westw.
(The halidaii of B.M. Catalogue has nothing to do with
this species. It is merely a small latreilliz.)
S. Ausrraxia (Adelaide). Type at Oxford.
TRANS. ENT. SOC. LOND. 1918.—PARTS III,IV. (MAR. 19) U
280 Rev. F. D. Morice’s Notes on Australian Sawflies.
36. (32) Legs and venter violaceous black. Tempora, scutellum,
and sides of abdomen, bright reddish-orange. Scutellum
unusually wide at the apex, its lobate processes far apart.
Length about 15mm. . . . .. jucunda, W. F. Kirby.
W. Ausrratia (Swan River). Type in B.M.
— Legs and venter at least partly paleorred. . . . . 87.
37. Hind tibiae not blackened at theirapices. . . . . . 38.
— Hind tibiae blackened at their apices . Sip ah ce
38. Legs and venter bright orange-red. Length about 13 mm.
amenaida = rufomaculata, W. F. Kirby.
This Q was described by W. F. Kirby as rufomaculata,
but Konow was right, I think, in treating it as the Q of
amenaida (3), which name precedes rufomaculata in Kirby’s
List.
ADELAIDE. Type in B.M.
— Legs and venter not reddish, but pale luteous. . . . 39.
39. Antennae scutellum and venter entirely luteous. Length
about 144 mm. Tempora, a pair of longitudinal streaks
behind the posterior ocelli, edge of pronotum very narrowly
and oblique lateral carinations of mesonotum yellow. Body
nearly dead-black, the abdomen having a very slight tinge
of metallic purple only noticeable in a strong light.
jurinei, Westw.
N.W. Austratia? Type (a g) at Oxford (2 in B.M.).
— Antennae, part at least of scutellum, and sides of ventral seg-
ments black. Abdomen with a very noticeably metallic
coloration, purple in some lights, blue in others; the pro-
podeum, however, the mesonotum, the pronotum (except
its luteous edges), and the dark markings on various parts
of the fulvous head are simply black. . semipurpurata, n. sp.*
Of two specimens in B.M. one (the Type) is larger,
fully 15 mm. long; its scutellum is yellow, bisected longi-
tudinally by a broadish stripe of black; its antennae
* Xyloperga semipurpurata, n. sp.
Caput fulvum nigro-variegatum; thorax niger luteo-pictus ;
propodeum nigrum, reliqui abdominis dorsum (exceptis lateribus
et apice luteis, pulcherrime metallescens (purpureo-cyaneum),
venter luteus nigro anguste marginatus. Pedes post coxas toti
lutei. Alae superiores lutescentes, inferiores albo-vitreae. Long.
15-12 mm. (Scutellum vel flavum nigro-vittatum, vel interdum
totum nigrum.)
Rey. F. D. Morice’s Notes on Australian Sawflies. 281
entirely black. The other is much smaller, only about
12 mm. long, and its scutellum is entirely black. (The
antennae in this specimen are broken, but what remains
of them is black.) In all other characters the two speci-
mens agree exactly, they were taken in the same place,
and I have no doubt that they belong to one species.
The smaller form is probably an aberration merely. If
a name be needed for it, it may be called semipurpurata,
var. melanaspis.
S. W. AustraiA (Yallingup). Types in B.M.
40. (37) Antennae entirely yellow. Middle lobe of mesonotum
margined with yellow, side-lobes and basal segments of
abdomen more or less rufescent. Length about 12 mm.
lalage, W. F. Kirby ( ?) *
— Much larger than lalage, and with the antennae not entirely
vellows =... Dee est tals
41. Antennae black DA tHe basal aint Middle lobe of the
mesonotum in the unique Type apparently entirely black
(but, being pinned through this part, it cannot be examined
quite satisfactorily). Not unlike a very large semipurpurata ;
the colour of the abdomen above is a fine rich purple, as in
that species, but the venter seems to be marked with black
only at its base, the scutellum has no black central vitta
(though the commencement of one seems to be indicated by
a little black triangle at its extreme base), and the head
above is almost entirely luteous between the ocellar area
and the occiput, with only a narrow black longitudinal vitta
bisecting the vertex, while in semipurpurata there are also
a pair of subtriangular black maculae running from the
occiput to the eyes and covering a part of their orbits. This,
except aurulenta, is the largest Xyloperga which I have
examined, fully 18 mm. long . . dentata, W. F. Kirby.
S. AustRAtra (Adelaide). Type in B.M.
— Antennae fulvous except the two basal joints and extreme apex
of each which are black. Middle lobe of the mesonotum
with a yellow mark in its posterior angle. Smaller than
dentata (about 16 mm. ne and with the metallic colour of
* The type of lalage is a 3 from Melbourne. The 2 which I
venture to associate with it was received in B.M. after Kirby’s
death, and is from a very different locality, viz. Cairns in N. Queens-
land. Still it appears to me conspecific with Kirby’s Type.
282 Rey. F. D. Morice’s Notes on Australian Sawflies.
but a sort of dark
indigo. The scutellum is yellow, with no black central
vitta, but bisected longitudinally by a sharply defined
the abdomen different
suleation. . . . . . . . . buyssoni, Konow (?)*
VICTORIA.
dd.
(For localities of spp., so far as I know them, see the
Table of 22 above.)
1. Third cubital nerve bent asin Pl. XV, Fig. 14. . . . 2.
— Third cubital nerve approximately straight . . . . . I5.
2. Hind tibiae considerably longer than hind tarsi (claw-joint
mmcluded), 5, “se Tai. Goes), STR BA fee sie ed
— Hind tibiae about as long as hind tarsi. . 1 Ore Pin fA
CHO
. Antennae of normal length, capitate, 3rd and folloaane joints
before the club distinctly separated, and never broader than
long “Kdindl ie Popa RA sete crt Ge Care eens me
— Antennae paradoxically short, more or less clavate from the
3rd _ joint onwards, the joints usually indistinctly separated
and broader (at their apices) than long. . . . . 12.
4. Intermediate segments of abdomen above clothed with dense
rows of pale decumbent hairs, the hairs in each row of equal
length and lying parallel to one another (longitudinally).
(A character not unlike this occurs in 3 3 of the non-Australian
genus Abia/) Large forms (about 20 mm. long in average
Specimens) 5. <2 8.0 & : Sy Ram oho! rr
— Intermediate segments of abdoten above Biabigus ae Lae 6.
. Head above and mesonotum (except its yellow seutellann)
unicolorous (metallic greenish). (Abdomen usually coloured
similarly, but one specimen in B.M. from Melbourne has
it entirely reddish!) Mesopleura with or without yellow
markings, but never perhaps entirely yellow (Type in B.M.).
dorsalis, Leach.
— Head and mesonotum coloured as in dorsalis, but mesopleura
entirely yellow, and abdomen with its sides and apex rather
brightly rufescent. (Whether the unique B.M. *“ Type’
from Tasmania really belongs to its supposed 2 and differs
specifically from dorsalis seems very doubtful)
affinis, W. F. Kirby.
* T have not seen the Type of buyssoni, which is presumably at
Berlin: but a single unnamed specimen in B.M. answers fairly
well to his description. The locality cited for it by Konow is
Tasmania.
Rev. F. D. Morice’s Notes on Australian Sawflies. 283
6. Scutellum bisected longitudinally by a deep and wide suleation.
Fore-wing with a conspicuous * patch of scale-like hairs
(situated on the underside of the wing, but visible through it
from above) which occupies part of the radial and cubital
AQEAS (Ee RIO ies Weer ste at awe ste ATF Of.
— Scutellum not deeply sulcate—at most with a slight central
impression. Fore-wing with no conspicuous aggregation of
hairs, as described above, though several species when
carefully examined seem to possess the character to a certain
extent, while others lack itentirely . . . be Lats 08;
7. The fore-wing only with a pilose patch as abuive described.
General colour of the insect testaceous brown, but the scu-
tellum distinctly yellow . . . . . . polita, Leach.
— Hind-wing with a pilose patch like ‘hai of the fore-wing but much
smaller. General coloration of insect darker, scutellum not
yellow but brown like the rest of the dorsal surface.
castanea, W. F. Kirby = divaricata, W. F. Kirby, 3, nec 2! 7
Type of divaricata in B.M.
8. Two basal joints of antennae black, the rest testaceous. Ab-
domen black above, sulphur-yellow beneath. Scutellum
testaceous (not yellow) with a more or less conspicuous
central suleation. . . . +f. wg .. antiopd, n.-sp:
— All joints of antennae luteous ee black !) Dorsum of abdomen
never black. (Scutellum may be yellow, or may differ from
that of antiopainits sculpture). . . .... . 9.
* Visible to the naked eye! It is very desirable that these hairs
should be examined in living specimens. They much resemble
the so-called androconia of some 3 Lepidoptera, and I venture to
suggest that they may have a similar function. This point cannot
be investigated to any purpose in old dried specimens. “ Aus-
tralian Entomologists, please note!” So far as I know, the exist-
ence of scent-scales in the wings has never yet been suspected in
any Hymenopteron, though it is well known that certain 3 Bees
have a peculiar fragrance (Psithyrus, etc.).
y The ¢ and 9 described together by W. F. Kirby (Ann. and Magq.
N.H., 1893, p. 39) as the sexes of a new species *“divaricata ”’ cannot
possibly be conspecific, their neuration showing that they belong
to different groups. Divaricata 3 I take to be almost demonstrably
the ¢ of castanea previously described from °° only by the same
author; and divaricata 2 is in my opinion a specimen of bella—it
certainly belongs to the bel/a group, as shown both by its neuration
and its saw-characters !
Kirby (/.c.) says he was “at first inclined to refer these specimens
to P. castanea, Kirb.” He did not do so because “in that species
the scutellum is much less thickly punctured.”
284 Rev. F. D. Morice’s Notes on Australian Sawflies.
No)
. Scutellum bright yellow, almost or quite impunctate and un-
sculptured my. aware ac Mas, Saeed Pec Dee ecm ee Se 1s
— Scutellum brown (or only obscurely yellow) with strongly
punchunedidisee ts ReMi. lee eel es OG ll.
10. Side lobes of mesonotum partly chalybeous . schiédtei, Westw.
— Side lobes of mesonotum entirely testaceous . klugii, West.
11. Puncturation of scutellum extremely dense and rugulose.
kirbii, Leach.
— Puncturation of scutellum scattered and irregular. agnata, n. sp.
12. Abdomen above and below dark violaceous. Hind legs with
femora tibiae (at extreme apex) and tarsi blackened. A
small form—about 12mm. long . . . dahlbomii, Westw.
— Abdomen for the most part testaceous above and below ._ 13.
13. Larger—about 174 mm. long. Scutellum with its entire apical
margin black. Abdomen with its intermediate dorsal segments
feebly but rather broadly infuscated above, the infuscation
looking somewhat metallic (greenish) in certain lights.
vollenhovii, Westw.*
Type at Oxford.
— Smaller—10 to 15 mm. long. Scutellum entirely yellow, or
with its apical lobes only darkened. (N.B.—In all ¢¢ of
this group the scutellar lobes are almost obsolete.) Abdomen
above after the propodeum either entirely testaceous or with
very slight and interrupted indications of a darker central
line. In some specimens (dubia, W. F. Kirby) the propodeum
is yellowish, in others—as also in vollenhovii—it is black. All
these colour differences are likely to be inconstant; and I
can only at present recognise one variable species in the
specimens before me Sai tieke Ss brullei, Westw.
= ritsemei, Westw. = dubia, W. F. Kirby.
Types of brullec and ritsemer at Oxford. Type of dubia
in B.M.
14. Antennae black; scutellum black except its yellow apex;
abdomen above chalybeous, (a beautiful steel-blue !) beneath
pale yellow. Hind tibiae with black apices.
guerinii, Westw. = sericea, W. F. Kirby.
Type of guerinw at Oxford. Type of sericea in B.M.
* Two 3d of this in B.M. were determined by W. IF. Kirby as
brullei, Westw. These specimens are from Queensland.
Rev. F. D. Morice’s Noles on Australian Sawflies. 285
— Antennae scutellum and abdomen all testaceous. Hind tibiae
without black apices-.. . . . . . ferruginea, Leach
= newmanni, Westw. = sellata, W. F. Kirby.
Type of newmanni at Oxford. Type of sellata in B.M.
The Type of ferruginea (B.M.) is a 9.
15. Antennae with only 5 joints completely * separated from the
apical club. Labial palpi with only 3 joints, maxillary
Wwitheonly a Sn eee ss Ap UES RSE Di GY
— Antennae with 6 joints somipletely Koparated from the club.
(Genus Xyloperga, Shipp = Heptacola, Konow). Labial palpi
with 4 joints, maxillary with6. . . . Eee 8s
16. Larger—about 14 mm. long. Wings Bia with yellow,
their margins with a faint greyish-purple infuscation. Abdo-
men belted with bright red over its 2nd and 3rd segments,
the following segments deep black.
gravenhorstii, Westw. = peletiert, Westw.
Type of peletier: at Oxford. The Type of gravenhorstii
—also at Oxford—is a 9.
— Smaller—about 11-12 mm. long. Wings and abdomen coloured
otherwise .. Bee ML TR cnr al oe oag en pri yh Ay Mckee a ie
17. Abdomen blackish ses more or less rufescent near the arti-
culations of its segments. At the sides and on the ventral
plates it bears conspicuous whitish markings. Clypeus and
labrum yellow. . . . bella, Newman = foersteri, Westw.
N.B.—The clypeus, especially when viewed laterally,
appears as though its apex ended on each side in a blunt,
but distinctly projecting, tooth ! (This is because tie
clypeus, before its apical margin which is slightly reflexed,
is impressed deeply at its centre but not at its sides so
that the corners are left standing up at a higher level
than the rest.)
N.B.—Both fore- and hind-wings, as in castanea, are
furnished with patches of scale-like hairs in the radial
and cubital areas !
Type of foerstert at Oxford. (It is, I think, certainly
the 3 of bella, which was described from a 9). There is
another specimen quite like it in B.M.
* By ‘‘completely” I mean ‘all round.” The club itself
sometimes appears more or less indented laterally (as though
jointed), but the indentation never runs completely round it !
286 Rev. F. D. Morice’s Notes on Australian Sawflies.
— Abdomen almost entirely red, with no white markings at the
sides or beneath. Clypeus black. A patch of scale-like
hairs occurs in the fore-wings only.* Apex of clypeus simply
rounded on each side, with no reflexed margin, nor appear-
ance of dentiform corners i ee ee es llatrenlakeach:
Type in B.M.
18. Abdomen with its basal half mostly luteous, the apical segments
only being chalybeous . . . XX. univittata, W. F. Kirby.
Co-types in B.M. (The Type is a 8.)
— Dorsum of abdomen practically chalybeous throughout. . 19.
19. Basal joints of antennae, hind femora, and apices of hind tibiae
blackened...° (50.2) owe cs” fans ke lalage Wo arby;::
Type in B.M.
— Antennae and legs altogether testaceous or luteous. . . 20.
20. Vertex shining and almost impunctate. Middle lobe of meso-
notum with a conspicuous V-shaped yellow mark defining
its posterior (= basal) angle. The scutellum is not entirely
yellow, its apical half being partly occupied by a subtriangular
impressed space of darker (brownish) colour.
(The puncturation both of head and thorax in this species
is much less close than in jurinei and the surface very much
more shining.) . . . . . X.amenaida, W. F. Kirby.
Type in B.M.
— Middle lobe of mesonotum only touched with yellow at its
extreme base (no conspicuous V-shaped mark !). Scutellum
entirely yellow.
Puncturation of head and thorax dense and “ granulose,”
the surface consequently appearing completely dull.
X. jurinei, Westw.
Type at Oxford. :
The other described forms of Xyloperga are all 99,
mostly unique specimens at Oxford or in B.M., and their
33 have yet to be discovered.
* This, at any rate, is the case with the Type; which, however,
is of course a very old specimen, though it seems in fair
condition.
Rev. F. D. Morice’s Notes on Australian Sawflies. 287
CEREALCES, W. F. KIRBY.
SYNOPSIS OF THE SPECIES.
The genus Cerealces is known only from Australia. It
contains two species only, both described by W. F. Kirby,
and of each 3g only have occurred. These may be
separated as follows—
Scutellum rufo-fulvous; hind tibiae entirely pale yellowish-
brown. Antennae 10-jointed, the joints except the two
first and the last distinctly (but not paradoxically) dilated
at their apices . . .* . . . scutellata, W. F. Kirby.
Type in B.M. “Soutu AvUSTRALIA.”
— Scutellum black (with only the tubercles at its apex yellow);
hind tibiae with black apices. Antennae 11- or 12-jointed,
the intermediate joints paradoxically expanded (cup-like)
at their apices. (The antennae of the Type are now un-
fortunately lost !) cae ve. an ecyaunrormis., WE. Karby:
Type in B.M. No precise locality is given.
PHILOMASTIX, FROGGATT.
SYNOPSIS OF THE SPECIES.
Two species of Philomastix have been described, namely
macleayui, Westw. (= glaber, Froggart), and nancarrowi,
Froggatt; the latter, by some oversight, is not included
in Konow’s list in Genera Insectorum. Westwood, as I
have elsewhere mentioned, mistakenly described macleayii
as a Perga, but this error does not invalidate the specific
name which he gave to it, and this therefore has priority
as against that proposed by Froggatt.
The species are practically identical in colour, at any
rate in the 99 (I have seen no dg of macleayi). But they
seem to differ considerably in size, macleayii being the
larger species, and also apparently always in the number
of antennal joints, as stated below. It is curious that, in
nancarrowi at least, the g antennae are shorter than the
©, and yet have more joints! See Pl. XII, Figs. 5, 6.
Westwood’s Type of macleayii is at erate ‘The Types
of nancarrowi and glaber are, 1 suppose, in Australia,
288 Rev. F. D. Morice’s Notes on Austratian Sawflies.
and of course I have not seen them, but two specimens
of * glaber 29” and many of nancarrowi JS and 9° are in
B.M. named by the author.
(exe)
+} f°
Stigma with pale (yellowish) apex. Antennae more than
15-jointed in the 2. Larger species.
macleayii, Westw. = glaber, Froggatt.
— Stigma entirely dark. Antennae only 13- or 14-jointed (the
apical joints are not very distinctly separated) in the 9.
Smaller species .. . . . . . . nancarrowi, Froggatt.
The very curious larva of Philomastix is figured in
Froggatt’s ‘‘ Australian Insects.” It has, like Perga, no
ventral legs and, unlike that or any other Australian
sawfly- larva, two paradoxically long anal appendages
(cerci 2). In both these characters “it seems allied to
the Pamphilidae, but in these the cerci are comparatively
quite short! I doubt, however, whether this similarity
is due to any special phylogenetic affinity between the
Australian and the Palaearctic species. The former is
much more probably a peculiar genus of the Pergidae,
with which it agrees in several characters (reduced number
of palpi, etc.) not found in any of the Pamphilidae.
(For the alar neuration of Philomastix see Pl. XI, Fig.
13.)
PERGULA,
I have only seen one species of this curious little genus,
and of that species only one specimen, a 3. It is, however,
so distinct that I venture to describe it.
A
Pergula turneri, n. sp. dg
Black, shining, feebly and shallowly punctured. Mouth-parts,
trochanters, knees, tibiae, tarsi, and genitalia sordidly whitish.
Apices of hind tibiae, and the tarsal joints following, more or less
infuscated. Wings hyaline.
Antennae very shortly pilose, 7-jointed; the apical joint about
as long as the two preceding it, and rather longer than joint 3.
The joints, except the apical and the two short basal ones, are all
obconical, and the antennae as a whole might he called subclavate.
Face subquadrate, inner margins of eyes parallel. Clypeus very
short (its apical margin slightly sinuated inwards), antennae in-
serted close above it. Frons deeply sulcate longitudinally from the
Rey. F. D. Morice’s Notes on Australian Sawflies. 289
anterior ocellus to the clypeus, it is also suleate on each side between
the supra-antennal carinations and the compound eyes. Ocelli
in a low broad triangle.
Fore-wings with the costa much dilated before the stigma, nearly
filling up the intercostal area, the latter with no visible transverse
nerve oz longitudinal vein dividing it. Radial cell without a
dividing nerve, and not appendiculate at its apex. Four cubital
cells present, the 2nd and 3rd each receiving a recurrent nerve
near its middle. Lanceolate cell wanting, as in Perga, etc. Hind-
wings with one closed cell (cubital); humerus present. Tibiae
without ante-apical spines, but with the hind calcaria extremely
long—longer than the metatarsi.
Length about 45 mm.
S. W. Ausrratia, Yallingup (near Cape Naturaliste),
taken by Mr. R. E. Turner in September or October 1913.
Type in B.M.
PTERYGOPHORUS, KLUG.
SYNOPSIS OF THE SPECIES.
The first Sawfly to be described from Australia was a
Pterygophorus, and the genus seems to be one of the most
abundant in most parts of that region, and also one of
the most striking both in colour and structure.
Its affinities are rather doubtful, but perhaps its nearest
relative is the Brazilian genus called by Cameron Lophy-
roides, and by Konow (wrongly, I think) Perreyia. Konow
associates 1t with the Northern group of which the best-
known genus is that called by Jurine Pleronus (from its
plume-like $ antennae) = Diprion, Schrank = Lophyrus,
Auctt. But its neuration in both wings is so very different,
that I think any relationship it may have to that group
must be extremely remote !
Since its larva has ventral pro-legs, and its palpi have
the normal number of jomts (4 labial and 6 maxillary),
it approaches more than Perga, etc., to the usual structure
of the Sub-order. In fact, its only real abnormality
seems to be in the matter of neuration, and in this it
agrees with Perga, etc., except in the complete disappear-
ance, or non-development, of a “second” cubital nerve
in the fore-wing.
See Plate XII for figures of the antennae (¢ and Q) in
290 Rev. F. D. Morice’s Notes on Australian Sawflies.
certain species, and Pl. XI, Fig. 12) for the neuration of
the wings.
OO
aha
1. Dorsum of abdomen, except its yellow apex, unicolorous—-
chalybeous or deep-black with no broad yellow or testaceous
markings. (Group OL;eyanets). 2 Ve ue eas ers (oem
— Dorsum of abdomen entirely testaceous, or broadly banded
with that colourjor with yellow i=. J. = =: s.-) ane
©
2. Pronotum and scutellum concolorous with the mesonotum—
chalybeous not testaceous nor yellow. Length of body
seldom ,exceéds: 20 sme 3) 0. As see Geta le inennes
— Pronotum and part at least of the scutellum testaceous or
yellow. Mostly large forms, 15 mm. long or more. . 4.
o
3. At least 5 consecutive segments of the abdomen are testaceous.
Wings (Pl. XI, Fig. 12) for the most part clear hyaline, but
distinctly clouded under the stigma—the clouding elongate,
extending a little beyond the apex of the radial cell. Costa
not concolorous with the subcosta but yellowish. Antennae
(Pl. XII, Fig. 10) not simply serrate as in most 2° of this
genus, but evidently pectinate though more shortly so than
those of the 33. . =. = analis, Costa = gaudialis, Konow.
— Only four consecutive abdominal segments are testaceous.
Wings more or less violaceo-fuscous throughout, but (as
usual in this genus) somewhat more so in the upper part
of the fore-wing. Costa and subcosta concolorous—fuscous.
Antennae (Pl. XII, Fig. 9) simply serrate.
uniformis, W. F. Kirby.
(QUEENSLAND (Mackay). Type in B.M.
4. About as large as analis and uniformis, smaller than the spp.
following. Abdomen, except its extreme base and the apex
of the saw-sheath, entirely testaceous. Middle lobe of
mesonotum narrowly yellowish at the sides. lore-wings
(N.B.) bisected transversely by a conspicuous dusky stripe
which runs from the stigma right down to the inferior margin.
A similar but smaller clouding covers the upper basal nerve
and fills the base of the wing, and the inferior margin is
clouded likewise. (The antennae in the only B.M. specimen
have only 12 joints, but this is probably exceptional. Brullé
figures the antennae of his Type as 20-jointed.)
bifasciatus, Brullé.
N. S. Wares (Tweed River) B.M. Coll. Tasmanta
(teste Brullé).
Rev. F. D. Morice’s Notes on Australian Sawflies. 291
— Larger, usually about 15 mm. long. Abdomen blackened at
least at the sides, or widely before the apex. Middle lobe
of mesonotum immaculate, entirely chalybeous. Fore-wings
with elongate (not transverse) clouding . . . . . 5.
5. Abdomen above black or cyaneous at the sides only. Antennae
entirely black. Stigma fuscous, costa testaceous. General
colour rather brick-red than yellow or orange.
interruptus, Klug.
All eastern AUSTRALIA and TASMANIA.
— Abdomen above with at least three of the intermediate segments
blackened right across. Costa and stigma yellow. General
colour inclining more to yellow or orange than to red (group
Git OAD). i teh oh SB BER ge : a ae
). Yellow banding of abdomen narrower, only one dorsal segment
_~
—the third—entirely yellow. Sixth segment black except
narrowly at its apex. Seventh segment black . . . 7.
— Bands of abdomen broader, and the colour rather orange than
yellow. At least the second and third segments and a part
of the seventh are of this colour. The fourth segment is
rarely entirely black, and when it is so the seventh segment is
entirely flavous. Generally both these segments are partly
black and partly yellow. (Whether these colour-differences
are more than subspecific seems very doubtful!) . . 8.
7. Apex of clypeus widely and angularly (but very obtusely)
Emarpinaten Sener) Gn ice ee 4 wcrncrus, Klug:
N.S. Wares (Woodford, etc.); Victoria; S. QUEENS-
LAND.
— Apex of clypeus in the unique specimen in B.M. truncate;
otherwise exactly like cinctus, of which it is possibly only an
individual aberration. (It is not a “subspecies,” having
been taken along with the typical form of cinctus !).
distinctus, Rohwer.
N.S. Wares (Woodford). Type in B.M.
8. Seventh dorsal segment of the abdomen, but not the fifth and
part only of the fourth, for the most part yellow.
insignis, W. F. Kirby.
Only known from QuEENSLAND (Mackay). Type in B.M.
—- Seventh dorsal segment black, fourth and fifth entirely yellow.
I have only seen one specimen of this form, viz. Mr. Rohwer’s
292 Rev. F. D. Morice’s Notes on Australian Sawflies.
Type. The author compares it with interruptus, Klug, but
it has little resemblance to that species and is evidently
much nearer to cinctus. (I am inclined, as is also Mr. Turner,
to regard all these forms (distinctus, insignis, and zonalis) as
specifically not separable from cinctus: but more material
is needed before the question can be positively decided).
zonalis, Rohwer.
QUEENSLAND (Mackay). Type in B.M.
9. Joints 3rd to 8th of the antennae pale yellow. Apex of clypeus
not bilobate, but sinuated inwards very slightly through its
whole extent. General colour deep-black with slightly
metallic (greenish) reflections on the abdomen, purplish on
the mesonotum, and brightly chalybeous on the face, except
the clypeus which is greenish at the base and violaceous
at the apex. Pronotum, scutellum and a very narrow (widely
interrupted) fascia at the apex of the propodeum pale yellow.
Wings yellowish, infuscated at their bases and in the radial
and cubital areas... we to turner Rohwer:
(YUEENSLAND (Cairns). Type in B.M.
— Antennae entirely black. Apex of clypeus bilobate. . . 10.
10. Basal half of fore-wings and the entire hind-wings nearly clear
and colourless, apical half only of fore-wings distinctly clouded.
Abdomen entirely chalybeous except its extreme apex, which
is yellow "s' o.f 49 2 we ne) ta) SR ieyanens leach
= leachii, Konow, nec W. F. Kirby.
VICTORIA.
— Wings brownish-violaceous throughout, though darkest at their
bases and in the radial and cubital areas. Colour of body
as in cyaneus of which it is very probably a “ subspecies.”
leachii, W. F. Kirby, nee Konow.
QUEENSLAND (Bowen, Mackay, Townsville). Type in
BM.
36.
1. Abdomen brick-red, with the apical ventral plate, the pro-
podeum and the two following segments, and (N.B.) a spot
on each side of segments 4th to 8th, chalybeous or violaceous-
* Leach does not mention the yellow apex of the abdomen, and
Konow therefore distinguishes cyaneus from leachii as not having
this character. But in fact the colour of the 9 abdomen is identical
in both forms, though in the 33 it does differ as stated by Konow !
Rev. F. D. Morice’s Notes on Australian Sawflies. 293
black. The pronotum, episternum of mesopleuron, scutellum,
and postscutellum yellow. Antennae black, with a pectina-
tion of 20 rays. (The Qis unknown.) . cygnus, W. F. Kirby.
W. Austratia (Swan River). Type in B.M.
— Abdomen differently coloured (especially without the lateral
spots on the intermediate abdominal segments !) . 2;
. Pronotum concolorous with the mesonotum—chalybeous . 3.
— Pronotum yellow, contrasting with the chalybeous mesonotum. 4.
3. Wings with a slight uniform brownish or. violaceous infuscation
throughout. Antennae longer than in the next species, with
more numerous (about 20!) but proportionately shorter
rays. These are about equidistant from one another through-
out, and grow shorter very gradually from the 10th joint
onwards.) 0: (. « s~s) s . -eiijormus, W: Kirby.
bo
QUEENSLAND (Mackay).
— Wings clearer, almost colourless. Antennae shorter, with
fewer (about 18) rays. These are closely packed together
near the base, but towards the apex become more widely
separated, and grow abruptly shorter from about the 14th
joint onwards tole. ttle ta oe, oh a analeCosta,
VICTORIA.
4. Abdomen with a broad red basal belt. Wings colourless, un-
clouded. Antennaeentirely black . . interruptus, Klug.
— Abdomen not belted with red. Antennae sometimes yellow,
entirely or only<at theirsbases 2 4° 5 (3 wD Ds
5. Abdomen belted with yellow
— Abdomen unicolorous, chalybeous or black ae
6. Fore-wings with a distinct elongate clouding along their upper
margins. Yellow belting of abdomen sharply defined.
cinctus, Klug, and (var. ?) insignis, W. F. Kirby.
— Fore-wings faintly brownish with no distinct marginal clouding.
Yellow markings of abdomen somewhat vague and indefinite.
leachii, W. F. Kirby.
Antennae with black bases. Wings coloured as in leachii, but
with a distinct small clouding under the stigma. Abdomen
cyaneus, Leach.
aS
-~I
chalybeous and shining. oS
— Antennae with yellow bases. Wings yellowish as in the 9, but
without conspicuous clouding. Abdomen black and dull.
turneri, Rohwer.
The 3 of bifasciatus is unknown.
294 Rev. F. D. Morice’s Notes on Australian Savflies.
DIPHAMORPHOS, ROHWER.
SYNOPSIS OF THE SPECIES.
Of this genus two species only are known; they were
both introduced and described in detail by Mr. Rohwer,
in Entomological News, vol. xxi, p. 474 (December 1910).
The 9 differ conspicuously both in size and colour
as follows—
29.
— Larger, length about 6 mm. Head, thorax, and abdomen
black without red markings . . . . nigrescens, Rohw.
Vicroria. Type in B.M.
— Smaller, length about 4 mm. Head and thorax black, but
abdomen with a broad red belt covering at least four conse-
cutive segments. (These °° superficially resemble small 33
of Clarissa divergens, but are naturally broader in proportion
to their length, and the antennae (Pl. XII, Fig. 11) have
more joints, and taper more towards their apices.)
minor, Rohwer.
NortH QUEENSLAND. Type in B.M.
dd.
The 3 of nigrescens is unknown. That of minor differs
from the 2 in having the abdomen entirely black, and also,
in such specimens as I have examined, in having 16-
jointed antennae, these in the 2 seem to be always
15-jointed.
EURYS, NEWMAN.
SYNOPSIS OF THE SPECIES.
Eurys and the genera most allied to it have been sup-
posed to be distinguishable among themselves by differences
in the number of joints in their antennae. But even in
the very limited material before me I find these differences
far from constant. Generally no doubt the number of
these joints in Hurys—or at any rate in its Q?—is 9.
But in one of the three 2 specimens of Z. laetus in BM.
the number is 10. It is 10 also in a specimen which Mr.
tohwer has ticketed as the ““ Type 3” of his n. sp. deceplus,
and in one of two others marked by him as * paratypes ”’
Rev. F. D. Morice’s Notes on Australian Sawflies. 295
of the same. Solely, it would seem, on account of this
character the species inconspicuus, Kirby, which in size
and colour is utterly unlike a normal Hurys and has also
a difference in its neuration, has been placed in this genus.
But here, too, a jin B.M. has distinctly not 9 joints. but 10.
(I have little doubt myself that this species is no Hurys,
but a Clarissa, and shall treat it accordingly !).
Again, Buryopsis, Kirby, is said to have 11-jointed
antennae, and this is true of the only two specimens (both
33) on which this supposed ‘“ genus”? has been founded.
But I am almost sure * that these specimens are really
the hitherto unidentified 3g of two Hurys species of which
22 only have been described. “ Huryopsis nitens,”
W. F. Kirby, I take to be almost certainly the ¢ of Hurys
laetus, and “ Euryopsis bella,’ Rohw., most probably the
gS of Burys nitidus. The number of joints in Clarissa
spp. varies even more. Of DEAS Miter ar oyion
have seen specimens with 10, 11, 12, and 13 joints pee
tively, and in the Type (at Oxford) of C. thoracica, n. sp.
the number of joints is 14. Neoewrys, Rohwer, is aid by
the author to be easily known by its 14-jomted antennae,
but in the Type of #. metallica the number of the joints
is 15. And in a g of another species from Mount
Wellington, Tasmania, it is 11 only !
Thus in the comparatively few specimens before me
the number of antennal joints in Lurys (as I should define
that genus) varies from 9 to 11, in Clarissa from 9 (or 10
if inconspicuus be not included) to 14, and in Neoeurys
from 11 to 15. Such a fluctuating character is practically
useless for determination of specimens, and even if 1
were more constant, I should hesitate to consider it of
really generic value.
On other characters, however, the three groups of
species, though closely allied, seem capable of being main-
tained as at least good subgenera, and perhaps as good
genera, though on the existing material I should not
myself have a einaced to erect ew as such. Thus—
Eurys (including Huryopsis) differs from Clarissa in the
brilliant metallic coloration of all its species, and also in
having the radial cell more distinctly appendiculated,
consequence of which its apex is not adjacent to the
margin of the wing. The same character separates it
* Tf I am mistaken in this, no 3 at all of Eurys have been
described !
TRANS. ENT. SOC. LOND. 1918.— PARTS III,IV. (MAR. 19) 3
296 Rev. F. D. Morice’s Notes on Australian Sawflies.
also from Neoeurys, with which it agrees in coloration.
And Neoeurys is also a smaller and much more slender
form, with evidently more elongate joints in its antennae,
and also in its legs—the hind tarsi (in particular) being
far longer in proportion to the tibiae.
The four forms actually known to me which I should
unhesitatingly refer to Hurys may be tabulated as follows
exe)
ap are
1. Abdomen entirely metallic, without yellow or whitish markings
at the sides or beneath. . . . : Reet
— Abdomen with the inflexed sides of its dorsal See margined
at their posterior corners with white or yellow. . . . 3.
2. Head, thorax, and abdomen metallic green or greenish-blue
throughout, with slight golden, fiery, or cupreous reflections
in certain lights. Femora not blackened at their bases
above but entirely testaceous orange, concolorous with the
tibiae and tarsi. Length about 7mm. . . /aetus, Westw.
Type (described as a “ Dictynna”’) at Oxford.
— Head and thorax reddish-cupreous throughout, densely punc-
tured and therefore somewhat opaque; the abdomen is dis-
tinctly greener, with little if any cupreous tint. Femora
evidently infuscated at their bases above. Rather smaller
than laetus—about 6 mm. long.
rutilans, n. sp. (= aeratus, W F Kirby! nec Newman ?)
W. F. Kirby called this specimen “ aeratus, Newm.,’
but it does not correspond at all well to Newman’s descrip-
tion, which particularly states that the head and also the
thorax are ‘“nigro-aeneous.” Aeratus was described in
1841 from two specimens in the Collection of the Entomo-
logical Club. That Collection was presented a year later
to B.M., so the Types ought to be there now. But if
they ever arrived there, they have long disappeared, for
no mention of them is made in Kirby’s List. (The present
specimen is certainly not one of the missing Types, having
been acquired at a much later date by purchase.) On
the whole I see no reason for identifying this form with
aeratus, Newm., and provisionally treat it as distinct.
Type in B.M.
The largest and most highly coloured of the forms. Length
about 8 mm. Head and thorax finely and rather closely
Rev. F. D. Morice’s Notes on Australian Sawflies. 297
punctured. Abdomen greenish at base and apex, but the
intermediate segments above are mostly rich purple, diversi-
fied with bluish, indigo, and green reflections in certain lights.
Beneath, the lateral white or rather pale yellow markings
are conspicuous and well defined, contrasting strongly with
the green surface of the ventral plates which they overlap.
The legs are testaceous or luteous with the apices of the hind
tibiae, and the tarsi more or less blackened.
nitidus, W. F. Kirby.
Type in B.M.
— Considerably smaller than nitidus. The white markings of the
abdomen are not so well developed, and its dorsum is nearly
unicolorous (metallic blue- (or sage-) green, and darker than
the thorax, which is brassy, sparsely punctured, and very
shining). The tibiae and tarsi are immaculate.
deceptus, Rohwer.
Type in B.M.
(In all these insects the labrum is more or less white, the
head and thorax delicately punctured, and the abdomen
has a very fine and close transverse striation. Without
more material it is impossible to be sure which of their
differences are really of specific value.)
NEOEURYS, ROHWER.
SYNOPSIS OF THE SPECIES.
In the original description of genus Neoeurys it was said
to be readily separated from its allies by the 14-jointed
antennae, but I have found variations in the number of
antennal joints in all genera of this group. And, in fact,
the Type of metallica in B.M. (a 2) has the antennae 15-
jointed, while in a 3 of another species the number of
joints is only 11.
The characters which seem to me best to distinguish
this genus from Hurys, with which alone it is likely to be
confused are: (1) the much shorter and broader face,
and (2) the more elongate joints of the hind-legs, particu-
larly the tarsi, which appear to be quite as long as the
tibiae, whereas in Eurys they are evidently shorter. It
differs also from Eurys as stated in my Synopsis of Genera
298 Rey. F. D. Morice’s Notes on Australian Sawflies.
(supra) in having the apex of the radial cell close to the
margin of the wing, and no definite appendicular cell
beyond it.
The B.M. collection contains at present 7 specimens of
Neoeurys, viz. (1) a 2 (the Type) of metallica, Rohwer, (2-4)
a g and two 99 taken by Mr. A. M. Lea on the summit of
Mount Wellington, Tasmania, (5-6) two gg taken by Mr.
Turner on the same mountain, but not near its summit
(these are considerably smaller than Mr. Lea’s 3, and I
doubt if they belong to the same species, and (7) a ¢ also
taken by Mr. Turner at Eaglehawk Neck—a very different
ae from the summit of Mount Wellington, namely
low-lying sandy isthmus on the coast of Tasmania,
(It does not appear to me identical with the specimens
from Mount Wellington, but on such material as I have
yet seen it appears safest to reserve judgment.)
I thought at first that Mr. Lea’s captures were sure to
be identical with Mr. Rohwer’s n. sp. fasmanica, of which
the 2 was taken apparently with them (cf. Ann. and Mag.
N. H., November, 1918). But I am now rather doubtful,
because Mr. Rohwer does not mention the most obvious,
though perhaps not most important, character, of the
B.M. 2 specimens—namely, the non-metallic pale reddish-
testaceous apex of the abdomen. If this character is not
constant, the B.M. 99 are probably tasmanica: and the
3 accompanying them, though larger than the male assigned
to them by Mr. Rohwer (w hich was taken at Eaglehawk
Neck, and is no doubt identical with Mr. Turner’s $ from
the same locality) unquestionably belongs to them. Not
having seen Mr. Rohwer’s Types, which are still in America,
I cannot clear up the matter; but provisionally I will
assume that his fasmanica Q is a different species from
Mr. Lea’s captures now in B.M., and propose in that case
to call the latter Neoewrys caudata, n. sp.
The 99 of metallica and caudata differ much in colora-
tion, as follows—
— Head, thorax, and abdomen concolorous, reddish cupreous.
The apex of the abdomen not differently coloured.
metallica, Rohw.
— Thorax and abdomen except its apex not at all reddish, but
black with a slight greenish (aeneous) tinge. The apex of
the abdomen not at all metallic, but pale testaceous.
caudaia, n. sp.
Rev. F. D. Morice’s Notes on Australian Sawflies. 299
In the g of caudata, which is very nearly as large as the
2 Ghont 4 mm.) the abdomen is unicolorous, blackish
from base to apex, the antennae 11-jointed.
The other gg had better, I think, remain undetermined
in the absence of any 9° with which they seem likely to
be associated. It salt probably be found that several
species (or at least subspecies) exist in Tasmania and else-
where. The Type of metallica is not from Tasmania, but
from Victoria.
CLARISSA, NEWMAN.
SYNOPSIS OF THE SPECIES.
Though the relationship between Clarissa and Burys is
evidently very close, they differ so markedly—at least in
the few species of each yet known to me—in the matter
of coloration, that it is easy to distinguish them at sight.
In Eurys this coloration is thoroughly metallic—as much
so as in many of the Chrysididae, whereas in Clarissa it
requires close examination to discover any tendency to
metallescence. The present metropolis of Hurys seems to
be West Australia, while that of Clarissa seems to be
rather North Queensland, and the only locality I can name
where both genera have yet occurred is the neighbourhood
of Adelaide. Striking as is this difference in colour, it is
perhaps of no very essential importance, for in many
Hymenopterous and other genera metallic and also non-
metallic species occur in the same regions. Still, as they
differ (though slightly) in neuration, and on an average in
the number of antennal joints, the distinction between
them may provisionally be treated as generic: yet it
would not be surprising, if the discovery of intermediate
forms should lead to a uniting of them at some future
time. But setting aside this possibility, which it is really
useless to suggest while so few of the imagines and none
of the larvae, ete., of either genus have been described, I
will proceed to a tabulation of such material as lies before
me.
++
Abdomen with no part testaceous, either black with white
markings,or black entirely <3 02) 3). 3 Sa 2. 2
— Abdomen red except at its (black) apex. . . . . . 3.
2. Thorax black; a large whitish mark on each side of the 2nd
300 Rev. F. D. Morice’s Notes on Australian Sawflies.
abdominal segment. Apex of clypeus, labrum, ete., tro-
chanters, and part of the tibiae whitish, the rest of the body
and legs black. Length of body about 7 mm.
atrata, G. Turner.
N. QUEENSLAND. Type in B.M.
— Thorax red; abdomen entirely black; apex of clypeus, labrum,
and legs luteous or testaceous—the tibiae and_ posterior
tarsi widely blackened. Wings rather cloudy, their neuration
and the stigma brown. The antennae of the unique Type
grevi4-jointeds 3) 2 ives “sg eM. clsuge | WROTACICOAE Sn:
“ AUSTRALIA” (teste Westwood). Type at Oxford.
3. Thorax above entirely testaceous. Antennae usually more than
10-jointed, but the number varies (10 to 13). Abdomen
testaceous with black apex. Length of body about 7 mm.
divergens, W. F. Kirby.
N. QUEENSLAND (Cairns and Mackay). Type in B.M.
— Prothorax red, but mesonotum almost entirely black. Antennae
usually 9-jointed, but sometimes 10-jointed. Abdomen
coloured like that of divergens. Much smaller than any other
species of Clarissa or Eurys, the largest 299 not above 4 mm.
invdength. 2s.) Sm 2 aneonspieums Wek. Barby:
(described as an Hurys).
N. QUEENSLAND, also Adelaide. Type in B.M.
Coy
I do not know the ¢ of thoracica. Those of the three
other species are coloured very similarly, black with tes-
taceous antennae and legs, and with the intermediate
dorsal segments of the abdomen more or less rufescent.
Inconspicua can be recognised at once by its tiny size,
barely 3 mm. long. In divergens the abdomen has a
broad red belt occupying at least the whole of segments 2
and 3 and often extending to segment 4. In atrata these
segments have their apices only red, but their bases black.
Both in divergens and atrata the antennae, and parts of
the legs (the femora and the apices of the tibiae and tarsi)
are somewhat infuscated; in cnconspicua this is not so.
All the $¢ are slightly shorter and considerably less broad-
bodied than their 99, and the prothorax in all of them is
entirely black.
Rev. F. D. Morice’s Noles on Australian Sawflies. 301
Note 1.—On the Distribution of Sawflies in general : the three
Zoological “ Realms”: and the probable origin of the
Australian Sawflies.
In this Note, and several of those which follow it, I
propose to avail myself on occasion of certain terms which
have been employed by Lydekker in his valuable and
suggestive little book A Geographical History of Mammals
(Cambridge Geographical Series, 1896). The principal
land areas of the KEarth are there divided into three
chief zoological *“* Realms,” namely, ARcroGAEA (= North
Land), NoroGaraA (= South Land), and Nkrocara
(= New Land), and the two first of these - Realms ” are
further divided into areas called “ Regions.” Though
originally founded on the Distributions of past and present
Vertebrate eroups, especially Birds and Mammals, and
entirely without regard to that of Insects, these divisions
seem applicable also to the present Distributions of Sawflies.
Of their former Distributions we know, unfortunately, next
to nothing. Such fossil remains of the Sub-order as have
yet been described, are too few, too imperfect, and of far too
recent date, to throw any considerable light upon the subject.
For our present purpose the limits of the three oreat
‘Realms’ will be sufficiently defined by saying “that
‘“ Neogaea’’ is nearly coextensive with such parts of
America as lie south of the Tropic of Cancer; “ Arctogaea,”’
besides including the rest of America, extends across the
Bering Straits and occupies all Europe, Asia and Africa
with their adjacent islands, except so much of the Malayan
Archipelago as les east of ‘‘ Wallace’s Line’; while
‘* Notogaea ”’ consists primarily of Australia and Tasmania,
which form a“ Region ” by themselves, but is also reckoned
as embracing three other isolated Regions, namely, (1)
the “ Austro-Malayan ”’ islands (especially New Guinea),
(2) Hawaii (the Sandwich Islands) and (3) ‘ Polynesia”
(New Zealand, etc.). Hawai and Polynesia, however, may
here be left out of account, for the former (as I learn from
Mr. Muir) has no indigenous Sawflies at all, and, with one
doubtful exception, the same is the case with Polynesia.
The Sawflies of New Guinea, Celebes, etc., are very little
known as yet, but some of them appear to be related to
Australian forms, though not actually identical with them.
Not much need be said here ag to most of the “ Regions °
included in Arctogaea, The largest and by far the most
29
302 Rev. F. D. Morice’s Notes on Australian Sawflies.
important is the “ Holarctic,’” which includes the greater
part of North America, all Europe, and the parts of Asia
and Africa adjacent to the Mediterranean Sea, Siberia, N.
China, Japan, and Central Asia. The parts of Asia nearest
to and north of Australia (India, South China, Sumatra,
Borneo, etc.) are the “* Oriental Region.” South Arabia and
South and Central Africa make up the “ Ethiopian Region.”
Madagascar is the centre of an isolated Region of its own.
And the “ Sonoran Region ” separates—or, rather, bridges
over the interval which separates—-Neogaea from Holarctic
America. The word “ Holarctic ” will occur frequently in
this Note, but the other Regions will seldom have to be
mentioned. [ know their Sawflies only from Museum
specimens, but if the inferences suggested by these can be
trusted, the differences between Holarctic forms and those
occupying other Arctogaeic Regions are not very striking
and negative rather than positive: 7.e. the latter are
characterised chiefly by the absence or extreme rarity of
groups which are dominant in the North, and the places
of these are filled not by other groups peculiar to the Region,
but by a further differentiation and increase of certain
particular genera which are well represented in the Hol-
arctic Region also. In Africa, for instance, and perhaps
throughout the Ethiopian Region, forms identical, or nearly
identical, with Holarctic Arge and Athalia spp. seem in a
manner to have made themselves paramount. (Pachylota,
Westw., originally described as from “S. Africa,” would
be a singular exception to the general rule, if we did not
know that this genus was really Neogaeic.) In the number
of well-differentiated “‘high’®’ divisions (Families, Sub-
families, etc.) included in—and often confined to—it, the
Holarctic Sawfly-Fauna far exceeds that of all the other
Regions taken together, and from this it is natural to infer
that the Sub-order has been longest established there, and
that somewhere in this Region was probably the original
centre of its distributions, the Sawflies of the other Regions
being really descendants of such Holarctic genera as have
overflowed into them and succeeded in adapting themselves
to the new surroundings. Any genus which could not do
this would remain, of course, confined to its original habitat,
or extend only in certain limited directions—chiefly east-
wards or westwards, such movements involving no change
of climate, ete.
But if, after comparing the Sawflies of various Arctogaeic
Rev. F. D. Morice’s Noles on Australian Sawflies. 303
Regions with one another, we proceed to compare them
as a whole with those of Notogaea, it becomes at once
apparent that we are dealing with far more substantial
differences. The line of demarcation between the two
eroups is almost as distinct as that which separates the
Mammals of the two Realms. We find, indeed, one single
Siricid (a Xiphydria) belonging to a genus which is repre-
sented by species not very dissimilar in the Oriental
Region, and by other species of slightly different appear-
ance (longer ovipositor, etc. !) in Kurope, and even in Ene-
land! We find also one true Svrex (manifestly imported,
for the natural range of this genus is exclusively Holarctic).
And we find, also, that one very common and mischievous
Sawfly, whose slimy slug-like larva is a notorious pest in
European and American orchards has reached, evidently
by unintentional and quite recent importation, both
Australia and New Zealand. We find lastly one small
insect which, though I believe it to be generically distinct
from anything in Arctogaea, has so many characters in
common Ww ith a well- known Arctogaeic genus, that 1t was
referred to it by the late W. F. Kirby and described as
‘““HynLotTomMa ”’ apicale,n. sp. But otherwise, so far as I
know, Australia and Arctogaea have not, a single really
native species, nor genus, perhaps not even one * Tribe ”
of Sawflies in common. It is not till we reach the higher
category of “* Subfamilies ” (according to Konow’s classifica-
tion in Genera Insectorum, ete.) that the Faunas of the two
Realms begin to show connection. Finding this we are
naturally reminded—though I do not mean to say that the
cases are precisely parallel—of the fundamental dissimilarity
between the present Mammalian Faunas of Australia and
Arctogaea. Apart from Bats, which in all such questions
must be left out of account—it is well known that not only
have these lands no native Mammals in common, but
that they differ even as to the “ Orders” represented in
them, the Mammals of Arctogaea (except one American
Opossum, which has spread northwards out of Neogaea)
being exclusively Kutherian, while those which are unques-
tionably native * (7. e. not importations) in Australia are
never Kutherian, but either Marsupials or Monotremes.
There is, in fact—** sv parva licel componere magnis *’—a
really curious and interesting parallelism in many respects
* Neither the “ Dingo” nor the Australian Muridae are ‘* un-
questionably ” natives.
304 Rev. F. D. Morice’s Notes on Australian Sawflies.
between the distributions throughout the world of Mammals
on the one hand, and Sawflies on the other. Thus (a) out-
side Australia (the N. American Opossum above-mentioned
excepted) Marsupials occur in Neogaea only, and there
also only we find Sawflies possessing certain characters
otherwise confined absolutely to Australian forms (no
“lanceolate cell,’ labial and maxillary palpi with a reduced
number of joints), and agreeing with them also in general
“facies” and coloration; (6) it is well known that the
indigenous Faunas of Oceanic islands include no Mammals
except Bats, and the same appears to be the case with
Sawflies, except the Timber-boring forms, which, like Bats,
have special possibilities of distribution; (c) the Faunas
of Madagascar and Arctogaea have at present, I believe,
only two Mammalian genera in common, and I can only
find one record of any Sawfly genus occurring in both,
viz. Athalia, except which no Sawflies at all are known
to occur in Madagascar, and Mr. H. Scott tells me there are
none in the Seychelles; (d) a few groups only of Mammals
(e.g. Canidae ‘and Felidae) have a pract tically world-wide
ae cabacon extending in one case to Australia; and simi-
larly among * Sawflies one remarkable eroup (the Arginae)
1s thoroughly cosmopolitan and has certamly reached
Australia. This may perhaps be the case with a few others
(Lophyrinae? and Cimbicinae?), but a majority probably,
both of Mammals and Sawflies, have their ranges strictly con-
fined between certain parallels of latitude, and this applies
not only to species but to genera, Tribes and Subfamilies ;
(e) lastly, though certain groups both of Mammals and Saw-
flies have reached their maximum of abundance and differ-
entiation in other Regions, it is pretty clear that the real
metropolis and original centre of distribution of Sawflies
must have been Holaretic, as was certainly that of Mammals.
Practically all the primary divisions of the Sub-order (and
of Hymenoptera generally) are well represented there, and
one at least (Lydidae, Konow = Megalodontoidea, Rohwer)
—as well as many flourishing Subfamilies, Tribes, and
genera of others—is apparently quite confined to that
Region. Therefore, though we have no palaeontological
evidence whatever as to the former habitats of existing
Sawflies or their ancestors, such as abounds in the case
of Mammals, it seems highly probable that the present
representatives of both groups, in any particular district,
have arrived in their present habitats from not very
Rev. F. D. Morice’s Noles on Australian Sawflies. 305
different centres of distribution by similar routes, helped
or hindered from time to time by similar causes. For
whatever physical barriers—such as seas, rivers, mountains
running east and west, deserts, intolerable climates and
temperatures, absence of certain kinds of vegetation,
etc., ete.—would present unsurmountable obstacles to
the migrations of a rather feeble and sluggish herbivorous
Mammal, would also restrict the distributions of most
genera of Sawflies; and, on the contrary, in both cases
such circumstances as sudden complete and Jong-continued
isolation in a favourable district through the disappearance
of land-bridges by which they had entered it would tend
to the rapid multiplication and differentiation into new
forms of some few stocks in that particular district, while
everywhere else they might be extinguished by the com-
petition with them of their superiors. Thus it is, perhaps,
not to be wondered at that Australia should have a Fauna
consisting, alike as to its Mammals and its Sawflies, of
genera and species apparently well-differentiated and fairly
flourishing, but representing a very small and probably not
the most characteristic part of—not the present Oriental
Fauna, but the Fauna which occupied that Region before
Notogaea ceased to be in contact with it !
Nor, when we reflect on the long ages that have elapsed
since that contact finally ceased, and the multitude of forms
that must have since been developed or become extinct
on both sides of Wallace’s Line, will it surprise us that the
present Australian Sawflies should no more resemble those
of the Oriental Region than those of any other part of the
world, or that the forms most resembling them should
happen to survive only in a country so distant as Neogaea,
Nearly the same has been the case with the Mammals.
And we may, perhaps, regard the phenomenon as some-
what parallel, though on a much larger scale, to that of a
country peopled throughout almost its whole extent by
certain dominant races, but with a few dwindling remnants
of tribes which had failed to hold their own in the interior
lingering on still, at points very far apart, in adjacent
islands, or headlands on its coasts... Alike in Australia and
in South America the southward migrations of Sawflies
appear to have reached their extreme limits; * the vegeta-
* T have sought in vain for any record of Sawflies from Patagonia
or South Chil’. Darwin’s collections made there and now in B.M.
include not one of that group !
306 Rev. F. D. Morice’s Notes on Australian Sawflies.
tion and climates of certain parts in both are known to
have something in common, and may be alike adapted
to the occupation of somewhat similar groups. The
Aculeate Family of Thynnidae is, I believe, also limited
to these two Realms.
To judge from the evidence of Distribution—and we
have really no other evidence to go by—it is hardly con-
ceivable that the Sawflies of Australia can have arrived
there otherwise than from Arctogaea, by way of the Oriental
Region, and travelling entirely overland. Even if, in very
ancient periods, ‘land-bridges > or “belts”? may have
connected Neogaea and Notogaea by way of Africa, or
Oceania, or an extension of the Antarctic Continent, we
do not know that at that time any Sawflies existed at all,
nor do any of the districts through which they would have
passed contain now, so far as is known, any evidence what-
ever of such migrations. Africa is the only one of them in
which at present any Tenthredinidae are normally to be
found, and not a single African Tenthredinid has the least
appearance of special affinity to Notogaeic or Neogaeic
forms: it is hardly too much to say that from Aloeria
and Egypt to the Cape the whole “facies” of every
species and genus indicates a comparatively speaking
not very ancient Holarctic origin! Agam, much as
the present Arctogaeic Sawflies differ in certain respects
from those of Notogaea and Neogaea, there is so much
essential agreement in the general structure and instincts
of the whole Sub-order, that it is impossible to doubt that
all must have radiated out from one original centre of
distribution; and it is most unlikely (taking all facts mto
consideration) that such centre was anywhere but in
Arctogaea. All that 1s most strange and exceptional in
the characters of Notogacic and Neogaeic Sawflies can be
probably accounted for by their long separation from their
Holaretic relatives, during which separation they have
lived under different conditions, and no doubt undergone,
in consequence, quite different modifications of structure,
instincts, etc., In successive generations; and, as might be
expected, the Notogaeic Sawflies are, on the whole, much
more abnormal than those of Neogaea, the former only
having been completely isolated since Tertiary times.
Although I have ventured to express the above opinions
with some confidence, I must admit that they rest mainly
on circumstantial and not altogether satisfactory evidence.
Rev. F. D. Morice’s Notes on Australian Sawflies. 307
The Sawflies of very few Regions have been collected and
studied to any considerable extent, and the known species
of any other are probably a very small fraction of those
actually existing there. This is especially true of South
America, except a few particular districts, and also of the
Oriental Region. For instance, up to December 1911 only
eight species representing seven genera of Sawflies (includ-
ing the Srricidae) had been recorded from Java; and then,
all at once, the captures made by a single Dutch collector
in one visit to the island doubled the number of its known
genera and brought that of its known species up to twenty.
It is also a significant fact that this collector's captures
ine'uded only one species that had been recorded from
Java before! (vide Enslin in Tijdsch. v. Ent. LV, 1912
p. 104). I have already alluded to another difficulty in
dealing with our present subject, namely, the want of any
palaeontological evidence as to the former range of any par-
ticular group. Without such evidence, as has been remarked
by Lydekker, many facts as to the present distribution of
Mammals would have been incapable of explanation, And
it seems only too probable that for lack of it many of the
points on which I have ventured to speculate must always
remain unsettled.
Note 2.—On Sawflies in general. The Characteristics of the
Sub-order, and the Groups included in it.
The Sawflies, if that word be used in its widest sense, are
a primary division (Sub-order) of the Order Hymenoptera
distinguishable from all its other Sub-orders by at least
two very definite and obvious differences, one in the struc-
ture of the imago, and another in that of the larva. In
neither case has this difference been developed within the
Sub-order uself. What has really happened, on the con-
trary, is that, whereas all the imagines of other Hymeno-
pterous groups have developed a character unknown in any
other Order, and all their larvae have Jost a character which
seems to have been formerly universal in the Class /nsecta,
the Sawflies, both as imagines and as larvae, have remained
true to the original type. A similar primitiveness, or
conservatism, may be noticed in other characters of the Sub-
order, especially in the venation of their wings, which @s
compared with that of all other Hymenoptera is remarkably
“generalised.” There is, on the whole, much more uni-
308 Rey. F. D. Morice’s Notes on Australian Sawflies.
formity and simplicity in their instincts and habits than is
found in other groups; they form no communities, nor, so
far as is certainly known, does “ inquilinism ” or ‘ com-
mensalism ”’ of any kind occur among them. We have,
perhaps, scarcely such evidence as would justify a positive
assertion that they are actually the oldest existing branch
of the Hymenopterous family-tree, but I can ‘point to
nothing either in their structures or in their lfe-histories
which would render this view improbable.
(a) The imaginal character which most definitely dis-
tinguishes the Sawflies from all other Hymenopterous Sub-
orders is the absence of any “ constriction” at the point
where the so-called “thorax”? joins the abdominal seg-
ments which follow it. But this so-called thorax in the
Hymenoptera includes, besides the three truly thoracic
segments, a fourth (the “ propodeum ”’) which has become
more or less incorporated with them during pupation, having
originally formed part of the abdomen. And it is really not
between the thorax and the abdomen, but between this
segment and the rest of the abdomen that the constriction
is situated. Accordingly, it might be correct to include
this segment always when counting the number of abdominal
seoments, and in the case of the Sawflies it is not unusual
to do so. But in dealing with other Sub-orders most
authors commence their enumerations after the constric-
tion, so that what is really the 2nd abdominal tergite
is called the Ist, and so on. Since this remarkable con-
striction (which enables Wasps, Bees, Ichneumons, etc.,
etc., to turn and twist in all directions the segments follow-
ing it, and thus bring their “stings ” to bear on any part
they please of any creature attacked by them) is a character
Re crien to Hymenoptera and not developed in insects
generally, its entire absence in the Sawflies * is clearly a
* Konow’s name for the Sub-order, which is adopted in Rohwer’s
Classification (1911), viz. Chalastogastra, meaning, I suppose,
(Hymenoptera) “ with unconstricted abdomen,” seems to describe the
real state of things more exactly than Lepeletier s Sessiliventres and
other names that have been suggested (e. g. Symphyta as opposed to
Apocrita), which imply that the thorax and abdomen are fused to-
gether. This, so far as the basal segment of the abdomen (= pro-
podeum) is concerned, is the case with all Hymenoptera! Another
name, employed in some other Papers of Rohwer, and of Enslin is
Tenthredinoidea, but for philological and other reasons I have a
special dislike to names formed after that pattern, and prefer to
accept Chalastogastra.
Rev. F. D. Morice’s Notes on Australian Sawflies. 309
case of “ generalisation ”’ and su
the group.
The larvae of all other Hymenoptera are footless, but those
of the Sawflies invariably possess three pairs of visible
thoracic legs—even in such cases as that of the Siricidae,
where these legs are feebly developed and probably quite
useless. Here, again, the Sawflies’ structure appears to
be more primitive, though the Hymenoptera are not the
only group in which the thorax of the larva bears no legs.
Also in the largest and most typical subdivision of Sawflies
most of the abdominal segments are furnished with pro-
cesses serving as legs (“ pro-legs’’) much like those of
Lepidopterous “ caterpillars.” Opinions differ as to the
origin of this character. Some have thought that the
ancestors of all insects possessed abdominal lees which
have now disappeared in all imagines and most larvae,
though they have survived in larvae of these two Orders,
but Handlirsch seems more likely to be right in holding
that in neither case have they been inherited from any
primitive common ancestors, and that such resemblance as
exists between the larval pro- legs of Lepidoptera and those
of certain Sawflies is merely “* analogous,” and consequent
on the similar habits and surroundings ‘of the organisms.
Although a great majority of Sawfly larvae possess them,
these all belong to one only of several distinct Families
or “ Superfamilies,” into which most recent specialists
divide the Sub-order. Larvae which at all times live and
feed concealed in wood (Sirex, Oryssus, ete.), or in buds,
stems, reeds, stalks of cereals, etc. (Cephus, ete.), or wrapped
up in rolled leaves, or silken webs (Pamphilius, ete.), never
have pro-legs, having, in fact, no need for them, as we shall
see presently.
(b) The character from which the “ Sawflies”’ receive
their vernacular name in English (and also in French,
sc. Mouches-d-scie) ‘is the serration or denticulation of a
part of their ovipositing organs, namely, the two bilaterally
symmetrical blades, placed side by side, and sliding freely
backwards or forwards along a supporting * ‘backpiece 7
this also consisting of two “bilaterally symmetrical parts,
not, however, freely movable, but bound together at
least at their bases, so that they must move together when
they move at all—with which they form receptacles for
their eggs. These blades have often a really striking resem-
blance to saws, and a part at least of their operations may
geestive of antiquity in
310 Rey. F. D. Morice’s Notes on Australian Sawflies.
fairly be described-as “ sawing.’ But there are two objec-
tions at least to considering this as the essential distinction
between this and the other Sub-orders. In the first place
all Hymenoptera (the Aculeates, Ichneumons, ete., included)
have their ovipositors so far saw-like that their apices are
armed with teeth, and are used for making their way
through the substances (whether animal or vegetable) on
which they are operating very much as a saw makes its
way through wood, ete., chiefly by help of its denticulations.
And, secondly, it is only in certain Sawflies that the organ
has really a saw-like appearance, with fairly broad blades,
and denticulations elsewhere than at the apex. In many
cases it is rather lancet-like than saw-like, scarcely to be
distinguished from the “ sting’? of a Wasp or an Ichneu-
mon, and in Oryssus, ete., it 1s “practically identical with the
terebra of a Cynipid. It may be added, that in all cases,
whatever be the general appearance of the organ, all its
parts are absolutely homologous —the sliding toothed
cutting-blades, their more or less connate ‘ ‘supports,’ the
attachments to the apical ventral segments, the complicated
arrangements by which the “ saws ” are started and guided
in their movements, etc., etc. The purpose for which their
operations are undertaken (namely, to prepare a suitable
“larder” or “ refectory,” which will provide an unfailing
supply of food for the expected offspring) is identical,
whether the insect be a Sawfly, or a Cynipid, or even an
Ichneumonid, or a Fossor,* for food is food, whether it
be animal or vegetable! On the whole, then, it is the
post-basal constriction of the abdomen, rather than any
character of the ovipositor, which really distinguishes other
Hymenopterous Sub-orders from the Sawflies.
There are, however, a good many other characters which,
at least in the order Hymenoptera, are exhibited by Sawflies
only; but most of these (e. g. (wo calcaria—instead of one
only—on the front tibiae) are not found in all eroups of the
Sub-order. Always, however, their wings have a greater
number of veins.+ and this should also indicate “ general-
* It seems to be only in the Social Aculeates that the organ is
chiefly used for other purposes, as a weapon rather than a tool, to
some extent merely for self-defence, but more for protection of the
community (by repelling enemies, extirpating its useless members,
etc., etc.).
+ Except in Oryssidae where the alar venation seems “ degraded.”
And even these have the “lanceolate cell,” which is peculiar to
Sawflies !
ee
Rev. F. D. Morice’s Notes on Australian Sawflies. 311
isation,” though it may be remarked that the wings of
extinct (fossil) Sawflies seem to lack certain veins which
are well developed in such living forms as come nearest to
them, and that long-isolated groups sometimes (as, for
instance, in Australia) have a distinctly less complete
neuration than that which prevails in Arctogaecic forms.
We shall presently see that certain veins are always wanting
in Australian genera, which are either invariably, or at least
generally, present in non-Australian Sawflies, and this and
other facts seem at first sight to conflict with the view that,
when a vein usually present is absent in certain cases, it
existed in them formerly, but has since been lost. I will
reserve this subject, however, till I come to deal in another
Note with the special peculiarities of Australian Sawflis.
Hitherto I have throughout been using the word “ Saw-
flies’ in its widest sense, including under it the two Lin-
nean “ genera —or, as most authors would now call them,
‘Families ”—Sirer and Tenthredo.* But it is often also
applied (with or without deliberate intention) to the latter
only, and in America—but not, I think, in England—
vernacular names have also been proposed for the former.
Comstock, e.g., in his well-known Manual (10th edition,
1912) distinguishes “* Tenthredinidae, Saw/lies,” from
“Siricidae, Horn-tails,’ and Rohwer (1911) writes on the
* Genotypes of Sawflies and Wood-wasps,” ete. In Germany
(from Panzer, Schrank, Christ, etc., onwards) many authors
have called them respectively “ Blattwespen” and “ Holz-
wespen” (= Leaf-wasps and Wood-wasps), but I doubt if
in this country we shall ever bring ourselves to call a sting-
less insect a wasp! To an En vglish reader the name Wood-
wasp would rather suggest a Hornet t (or perhaps a “* Vespa
sylvestris’) or some such creature as a Pemphredon or a
wood-boring Crabronid.
But to proceed: whatever names we are to substitute
for Tenthredo and Sirex as originally distinguished by Linné
(and for the moment I shall follow @ omstock i in calling them
respectively Tenthredinidae and Siricidae), the differences
between the two groups are very important, and suggest a
* The ‘‘ Law of Priority’ as at present interpreted has made it
necessary to restrict both these names to a few only of the species
originally included in them, and unfortunately both of them have
been restricted to different groups by different authors. How-
ever, as none of these groups contain any Australian species, except
the (imported) Sirex, or * Paururus,” or “ Urocerus,” juvencus, no
more need be said here on this subject.
TRANS. ENT. SOC. LOND. 1918.—PaRTs III,1V. (MAR. 19.) ¥
312 Rev. F. D. Morice’s Notes on Australian Sawflies.
number of questions which I have found very interesting
even when I have failed in answering them to my own satis-
faction. Let us inquire, then, how the typical members
of these sections differ—first, as to their Bionomics (= the
life-history of the individuals in each group), and afterwards
in other ways, some of the latter differences being apparently
consequent on the former.
(a) The food of their larvae differs, though in both cases
alike it consists exclusively of vegetable tissues. The
typical Siricidae feed on timber of some sort, perhaps never
quite sound and sometimes actually rotten; the Tenthre-
dinidae on fresh leaves, which in some cases are devoured
entirely, in others merely skeletonised, or more or less
emptied of their ** parenchyma.”
(b) The special mark of the Tenthredinidae, however, is
not so much the precise nature of their food—tor leaves are
also eaten by certain genera (Pamphilius, ete.) which in
other respects differ considerably from any typical Tenthre-
dinid—as the circumstances that (i) they are able to move
freely about the substances on which they are feeding, and
that (ii) while thus moving about they are usually fully
exposed to view, or at most imperfectly screened by the semi-
transparent cuticle of a leaf within whose interior they are
feeding. Larvae of Siricidae, on the contrary, issuing
from eggs deposited at the bottom of a deep and ‘extremely
narrow hole in the interior of timber, find themselves
hemmed in on all sides by material through which they can
only pass by gnawing a tunnel out of it with their jaws,
and afterwards forcing themselves forwards into this tunnel,
so as to continue the operation, with the help (as it is
believed) of a sort of horny spike, which arms the other
(anal) extremity of their body. Continuing this progress,
which must, of course, be slow and practically always in
one direction, they gradually pass by a tunnel which grows
wider and wider as they themselves increase in size “from
the interior of the timber towards the world outside; but
do not actually emerge into it. till they have completed their
metamorphoses and are no longer larvae but imagines.
Accordingly, (1) their movements are not free, but severely
limited, and (ii) they are under cover, and indeed buried
in absolute darkness, during the whole of their larval
life.
(c) Evidently connected with these differences in the
bionomics of the two groups are certain other differences
Rev. F. D. Morice’s Notes on Australian Sawflies. 313
namely of structure and general appearance—exhibited
almost without exception in their larvae.
(1) The free movements of Tenthredinid larvae are greatly
assisted by their possession of well- developed thoracic legs,
jointed, and armed with claws, and also of “ abdominal pro-
legs ”’ more or less like those of Lepidopterous caterpillars,
not indeed so elaborately constructed, but generally more
numerous (six pairs at least, and most commonly eight).
So far as is yet known, it is a rule to which, outside Australia,
there are no exceptions, that whenever the larva of a Saw-
fly feeds on leaves openly and moving freely about them,
it possesses abdominal pro-legs. On the other hand, such
pro-legs never occur among the Siricidae, and even their
thoracic legs are ill developed and jointless. Nor are pro-
legs developed in’ Pamphilius, ete. (whose larvae feed on
leaves, but keep always under cover, spinning silken webs
or rolling about themselves (like Tortricids) cases formed
from portions of the leaves on which they are feeding; nor,
again, in the Cephidae which feed not actually im dood,
but as a rule out of sight, in buds, berries, corn-stalks, hollow
or pithy stems, reeds, etc., and appear to be, both in habits
and structure, at least as nearly related to the Siricidae as
to the normal Tenthredinida.*
(1) The open life of a Tenthredinid larva exposes it to
many accidents and attacks of enemies, against which a
Siricid is to a great extent protected by its surroundings.
Hence in the former group many self-protective instincts
and “characters”? have been developed, which would be
useless and are unknown among the Sirzcidae. Such, for
instance, are habits of dropping out of sight when alarmed ;
lurking wnder a leaf, when not actually feeding; emission
of nauseous odours and secretions ; assumption of “threaten-
ing attitudes,” etc. Many species again have developed
protective colorations, cryptic or aposematic, etc., ete.
Nothing of the kind, naturally, is to be found among the
Siricidae. Tis probable that their larvae have no instincts
but such as are common to all insects at that stage (feeding,
moulting, preparing in due course to pupate, and so forth) ;
and, like most animals which live absolutely in the dark,
* In one or two (non-Australian) genera, which on the whole must
be reckoned as Tenthredinidae (Phyllotoma, Kaliosysphinga, ete.)
the pro-legs are ill developed, though never perhaps entirely wanting.
But these are leaf-miners—internal feeders—and therefore no excep-
tions to the rule as stated above !
314 Rev. F. D. Morice’s Notes on Australian Savflies.
they are practically colourless, and would gain no im-
munity from any dangers by “ mimicry,” ete., or formidable
appearance, or disouises of any kind. Against the only
enemies likely to assail them (Ichneumonids, carnivorous
beetles, centipedes, etc.) they are protected to a great
extent by their surroundings; and if these fail to save
them, they can only succumb. Disguises assumed in the
midst of darkness would not help them, and they cannot
take refuge by leaving their burrows.
(11) Siricid larvae, with one doubtful exception, are said
to be always eyeless; whereas those of T'enthredinidae have
invariably a sinele pair of ocelli, one on each side of the head.
The connection of this difference with their different modes
of life is so obvious that it needs no comment. But it may
be added, that in the Cephidae eyes are not wanting, though
they are said to be very small. In Pamphilius, ete., they
are present and well-developed; and as these, though feed-
ing under cover, do not live in actual darkness, we have
every reason to suppose that eyes are useful to them.
(2) The different bionomics of the two groups have a
certain effect on the structure not of their larvae only, but
of their imagines. In order that a Siricid egg may be intro-
duced into such surroundings as will suit the larvae which
is to issue from it, the ovipositor of the 2 parent must
be of considerable leneth. Its function being simply to
pierce, any unnecessary breadth or thickness would render
it less serviceable, and yet it must be armed (at least near
iis apex) with something in the nature of saw-teeth that
it may make its way through a certain amount of resistance
in the material to be penetrated. Accordingly the terebra
of a 2 Siricid is long—sometimes paradoxically long !—-
and narrow; its paired blades are shaped like fine needles
which have been more or less flattened to give them cutting
edges; and these cutting edges have a few minute denticu-
lations just before their apices. (In the Oryssidae the whole
apparatus is so phenomenally slender that it might almost
be mistaken for a long fine hair!) Even in those cases where
it is shortest—as, for instance, in Derecyrta, Brachyxiphus
and certain spp. (chiefly Oriental) of Xiphydria—it still
projects to a considerable distance beyond the dorsal apex
of the abdomen, and, even when at rest, cannot (as in
Tenthredinidae and also in Bees, Wasps, ete.) be drawn
backwards completely out of sight. A certain amount of
protection, however, is usually given to it by a modification
Rev. F. D. Morice’s Notes on Australian Sawflies. 315
in the form of the last dorsal seement. This is constricted
laterally and drawn out into a kind of spine which over-
hanes the base of the terebra, and is often jagged at the
sides in a manner which suggests that it may play some part
in the operations of the latter. (In the Oryssidae, however,
the last dorsal segment is simple, but in these the terebra,
though actually longer than the abdomen, is so slender and
elastic, that it can be bent back at its base, and packed
away out of sight in the abdomen itself. This Family, as
several authors have remarked, seems to be a link between
the Chalastogastra and other Hymenopterous groups,
especially, I would suggest, the Cynipidae.)
The ovipositions of the Tenthredinidae are made quite
otherwise. Here the eggs are to be so placed that the free-
moving larvae may pass at once after hatching to the
leaves which will form their food. There would be no gain,
but the contrary, if the eggs should be sunk any more
deeply into the food-plant than suffices to keep them in
position till the larvae emerge from them. They are
deposited accordingly, never at any great depth, in a sort
of sht or pouch formed by the terebra of the © parent
between the transparent cuticle of a leaf (or steak and the
tissues underlying it. The terebra best adapted for cutting
out such a receptacle need not be particularly long, and
extreme slenderness would be actually undesirable. As a
matter of fact, the form of the pouch, and the manner of
its formation varies considerably in different cases, and
though the “saws” of all Tenthredinidae have a certain
family -likeness they differ exceedingly in details for reasons
which have yet to be discovered. But, at any rate, they
are always much broader and thicker in proportion to
their length than those of any Siricid, armed with many
more denticulations, and altogether departing much more
from what seems likely to have been the primitive type of
an ovipositor. They seldom extend beyond the apex of
the abdomen, and are never too long to be completely
sheathed, when not in use, within the modified last ventral
segments. The dorsal segments seem to be little if at all
affected as to their shape rand size by their vicinity to the
ovipositor. Occasionally they are slightly compressed
laterally in the anal direction, but never so as to form an
actual spike, and they may usually be described as simple.
We have now seen (1) that to a certain extent the different
manner of oviposition in the two groups seems to be actually
316 Rev. F. D. Morice’s Notes on Australian Sawflies.
necessitated by the different requirements of their larvae
in the matter of food; (2) that in each case it determines
in part the surroundings, and consequently the habits and
even the structures of the larvae, and (3) that it requires
in each case a different modification in the terebra of the 9
parent, and of the abdominal segments to which the terebra
is attached. It appears also to have another consequence,
namely, that it affects the possible distributions of genera
and species in the two groups.
A Siricid larva may be and often is conveyed alive and
unhurt from one Region or even Realm to another, under
circumstances which would make such transportation
prac.ically impossible in the case of a Tenthredinid. Very
rarely indeed certain species of the latter group have
passed into and become established in a new district other-
wise than by their normal methods of dispersal, carried
unintentionally by human agency over barriers which they
could never otherwise have surmounted, e.g. across sea-
straits, and even oceans. Whenever this is known to have
happened, it is generally known that their food-plant was
transported also. * And it seems almost impossible that such
transportation should be successful unless the ae
insect happened at the time to have “spun up” or “ gone
down ”’ for pupation. Neither the exposed ae nor the
imago would be likely to survive a violent disturbance of
all its normal surroundings, and the life of the latter is
* In illustration of this two cases may be cited. (a) The Nematid
Pteronidea tibialis—an American species—occurs quite commonly
in Europe feeding on Robinia pseudacacia, a tree belonging to an
exclusively American group. This tree was introduced for the
sake of its timber on a very large scale by the celebrated William
Cobbett. (He sold 40,000 specimens to the then Lord Folkestone
for planting, cf. his Rural Rides.) Within a few years it became
distributed far and wide, and now abounds in all Western Europe.
Not long afterwards the insect made its first appearance in England,
and was described as tibialis, n. sp. by Newman. Subsequently, in
the same year, Hartig recorded it (under another name) as hortensis,
n. sp. from Germany.
(6) The only Tenthredinid common to New Zealand and Australia,
or to either of these regions and any other, is Caliroa limacina, Retz.
Though described from New Zealand as a new indigenous species
under the name Monostegia antipoda, W. F. Kirby, it is undoubtedly
the mischievous species whose ugly slimy larva has been a nuisance
to all fruit-growers for at least a century and a half, both in Europe
and North America, and there can be no doubt whatever that it
has reached Australia through the importation of Holarctic fruit-
tiees.
Rev. F. D. Morice’s Notes on Australian Sawflies. 317
under.any circumstances exceedingly short. On the other
hand, Siricidae are constantly imported, as larvae (in
timber) over great distances on shipboard, or by rail, ete.,
and when the transportation involves no great change of
climate they often become established in the new habitat,
nor 1s it necessary that material for their future ovipositions
should accompany them, for such is sure to be found wher-
ever they may go. This, no doubt, helps to explain why
the range of some S7ricidae is practically world-wide, even
when they cannot be said to be abundant anywhere, and
why the distribution of others is so extraordinarily “ dis-
continuous,” whereas that of Tenthredinidae, whether their
range be wide or otherwise, is almost always strictly “* con-
tinuous.” At the same time there are probably reasons
why the normal dispersals also of Siricidae should be less
restricted than those of Tenthredinidae. The imago of
the latter is commonly a soft-bodied, feeble, and rather
clumsy and awkward insect, timid and inert, incapable of
bearing rough usage, and disinclined to change its quarters
without necessity—in fact, its whole life is often passed on
or near the plant, on whose leaves it had fed as a larva.
Its wings, though ample, lack rigidity, and are usually far
less well adapted to prolonged flichts than those of a Siricid,
even if it Lad instincts prompting it to undertake them.
The mere fact that its migrations would generally be only
from one leaf to another of the same plant, or from one plant
to another of the same sort growing hard by, would naturally
make its dispersal slower than that of a Siricid, for the °°
of that group seem not unfrequently to oviposit at a con-
siderable distance from the timber out of which they have
emerged. They seem, too, altogether better adapted for
rambling afield than most Tenthredinidae. Their bodies
are harder, their wings stronger, and their speed, strength,
and often somewhat formidable appearance may carry
them safely over areas which it would be dangerous for a
Tenthredinid to enter. It may be remarked also that the
Siricidae whose distributions are most ‘ discontinuous,’
belong to a group (Oryssus, Ophrynopus, etc.) whose species
are rarities everywhere, and may probably be approaching
extinction. It is still represented by at least one or two
species in all Regions, and there can be little doubt that
it was once a flourishing Family. Most of its characters
appear to be exceedingly primitive, those of the ovipositor,
etc., being remarkably ‘ oeneralised ”’; others, however—
318 Rev. F. D. Morice’s Notes on Australian Sawflies.
as the defective neuration of its wings—are suggestive
rather of ‘‘ degradation.” On the whole, it seems likely
that this is one of the oldest, and perhaps the very oldest,
of all groups included in the Sub-order, and the diseon-
tinuity of its distributions may simply be due to its extine-
tion in the intervening areas. Yet it is certaimly very
puzzling, and to my mind even inexplicable, that Ophry-
nopus should occur only in Notogaea and Neogaea, and
should be represented in these very distant Regions by
forms which can only just be distinguished specifically,
unless we suppose that some unknown cause has interfered
with its natural dispersal. I believe, too, that one of the
two recorded European spp. of Oryssus (unicolor, Latr.) is
really an American form; and Enslin has lately described
another sp., closely allied to the only other European
sp. (Abietinus, Scop.), from a most unexpected locality—viz.
the interior of Africa !
For the two-fold division of the Sub-order adopted by
Linné, later systematists generally substitute one which
recognises either three ‘‘ Families” (Konow) or four
“ Families ” (Enslin) or four “ Superfamilies ” (Rohwer).
The two latter authors agree in separating the Oryssidae from
the Siricidae, whereas Konow kept them together. These
two groups differ greatly in the structural characters of
the imago, but the larvae of Oryssidae seem to be entirely
unknown, and though we may be sure that they live enclosed
like Scricidae in timber it has never been ascertained
whether or no they feed on it. For certain reasons it has
sometimes occurred to me that they may be parasitical,
and I find from Rohwer’s Studies of this group (1912) that
the same idea has suggested itself to others. I, however,
their structure and habits should prove to be identical with
those of Siricid larvae, I incline to think that the agreement
between the two-groups would outweigh their differences,
and at any rate that these differences ought not to be
treated as equivalent to those which separate both alike
from the Tenthredinidae. It might be well, perhaps, to
leave this question open for the present, until Oryssid
larvae have been discovered, and their structures and life-
histories elucidated.
The chief point on which systematists now differ is as to
the place which should be given in classifications to two
groups whose habits and structure seem to be hardly those
of either true Siricidae or true Tenthredinidae—namely,
Rev. F. D. Morice’s Notes on Australian Sawflies. 319
the “ Lydini” and * Cephini” of Konow. To explain the
points at issue we may begin by recapitulating briefly the
most conspicuous peculiarities of these groups. I have
alluded to most of them already.
The imagines of Cephini, superficially at least, much
more nearly resemble Siricidae than Tenthredinidae. They
agree with the former also in having one calcar only on the
front tibiae, whereas the Lydini and the Tenthredinidae
have two. Their ovipositors are much shorter than in most
Siricidae, but of a somewhat similar type; narrow through-
out, with comparatively few and simple denticulations
shaped like those in the “stings” of Bees and Wasps;
and they are generally more or less exserted. Their hind
tibiae in most genera are armed (besides the calearia) with
other spines before their apices. In this they agree with
the Lydini, but differ from Siricidae and also from most
Tenthredinidae, though certain genera of these latter (chiefly
Notogaeic and Neogaeic) possess such spines. Their larvae,
hke those of Szricidae, have no abdominal pro-legs, but,
unlike them, they have a pair of small and simple eyes.
These characters taken together would suggest that they
were nearer to Svricidae than to Tenthredinidae, and might
be an aberrant group of the former. Many authors, in
fact, have so treated them.
The imagines of Lydini, on the contrary, have hardly
any resemblance to those of Siricidae; but superficially,
and also in a character of some importance (front tibia with
fwo calearia), come much nearer to the Tenthredinidae. A
detail of structure, however, in the thorax which they share
with the Cephini, distinguishes them from the Tenthre-
dinidae. But it also separates them from the normal
Siricidae. Their ovipositors are small and little developed
in any way, but more like those of Tenthredinidae than
of Siricidae. Their tibiae are more copiously spined than
those of any other group, and this especially distinguishes
them from any normal S7zricidae. Enslin, calling attention
to their bi-calcarate front tibiae, tabulates them as Tenthre-
dinidae, but treats the Cephini as a Family apart (Cephidae,
Ensl.), though he remarks on their lkeness to Siricidae.
Konow, however, and also Rohwer, form one Family, or (as
Rohwer calls it) Superfamily (Lydidae, Konow = Megalo-
dontoidea, Rohwer) out of the Lydini and Cephini. I
thought at one time that Enslin was certainly wrong in
associating the Lydini with the Tenthredinidae, because the
320 Rev. F. D. Morice’s Notes on Australian Savwflies.
whole structure and bionomics of their larvae differ pro-
foundly. Larvae of Lydini have no abdominal pro-legs,
they have a most singular and characteristic development
of certain anal appendages (cerci), i both which characters
they seem more “ primitive” than normai Tenthredinidae ;
and though they feed on leaves, they are all the time con-
cealed in rolled leaves or silken webs, one such web being
sometimes spun in concert by a whole brood of larvae
feeding together gregariously. But my confidence on the
point was shaken when I found that several Australian
larvae, which seem to be Tenthredinid, possess no pro-legs ;
that one of these (Philomastix) has also anal cerci developed
even more paradoxically than those of the Lydini; and
that the larvae of a certain Neogaeic Tenthredinid (Dielo-
cerus) are stated by Curtis to spin up gregariously in a sort
of joint-cocoon (Lr. Linn. Soc. Lond., 1844, p. 248). The
imagines of the Australian species above mentioned have
ante-apical tibial spines as well as the usual “ calearia ”
and putting all these facts together, I am tempted to think
that both these latter and the Lydini may have inherited
these characters from primitive Tenthredinid ancestors who
had not yet completely developed the structures and habits,
which have now become almost universal in the Family.
At present, therefore, | cannot bring myself to follow Konow
and Rohwer in uniting the Cephini with the Lydini as a
single Family or Superfamily apart from and on a level
with the Siricidae or Tenthredinidae. It seems to me
more probable that the Oryssidae, Siricidae and Cepidae
are subdivisions of one main group from which the Tenthre-
dinidae should certainly be excluded. The Lydini (= Pam-
philinae, Ensl.) may perhaps represent a primitive group of
Tenthredinidae which had branched off from the main stock
before it had developed certain characters (especially
abdominal pro-legs in the larva, and the manner of feeding
connected therewith) which are now almost universal in it
—a few species, all Australian, being the only known excep-
tions. But even if this be true, it must remain a mere
hypothesis in the absence of palaeontological evidences to
support it, and such evidences must be admitted to be
wholly wanting. Such little knowledge as we possess of
the earliest representatives of the Sub- order has been care-
fully gathered and summarised in Handlirsch’s great work
on Fossil Insects. But the results at most indicate—it can-
not be said that they prove—that the Siricidae are a more
Rev. F. D. Morice’s Notes on Australian Sawflies. 321
ancient group than the Tenthredinidae. The former are
represented in Secondary (Jurassic) strata by several forms
which are referred to an extinct genus, Pseudosirex, and
by a single very peculiar fossil, originally, but (teste Hand-
lirsch) w rongly, described as an Ichneumonid (E':phialtites).
If this be really a Sawfly it must, I suggest, have been an
Oryssid. No Tenthredinidae or Pamphilinae occur in these
strata, and no Sawflies of any kind have been found in those
of Cretaceous or Hocene times. It is not till after the
earliest division of the Tertiary period that Tenthredinidae
and Pamphilinae begin to appear, namely, in the Oligocene
deposits, and as most of these fossil forms are stated (some-
times, perhaps, in error?) to belong to well-known existing
genera, they cannot be relied upon as fixing a date before
which these eroups cannot have come into existence. It
is quite likely that they were already well established in
Eocene times at least, and perhaps in Cretacean, or even
earlier, for Siricidae certainly must have existed all through
these periods though we have no records of them, any more
than of the Tenthredinidae ! What is the precise relation-
ship between these great groups can as yet be only con-
jectured. Judging from their “ characters °’—and we have
nothing else to judge by—we may suppose that the Scriecdae
are the earlier group, but whether the Tenthredinidae and
Lydinihad Siricid ancestors, or whether Siricidae + Cephini
+ Oryssidae and Tenthredinidae -+- Lydini are respectively
earlier and later branches of a common stock are questions
which must here be left unanswered. Of one thing we may
reasonably feel sure, viz. that the earliest Tenthredinid and
Lydine genera were not differentiated exactly as are those
which now exist, and that therefore those representatives
of them that have been described from Oligocene deposits
are not the first generations of these Families. The original
ancestors may yet be discovered in earlier strata, or may
never be discovered at all.
Note 3.—Characters of Australian and non-Australian Saw-
flies compared or contrasted.
If, as I believe is the case, the Sawflies of Australia are
all descended from Holarctic ancestors, it is natural enough
that we should be able to recognise among them far fewer
distinct and strongly characterised groups, than in many
Holarctic regions of an extent equal, or inferior, to that of
322 Rev. F. D. Morice’s Notes on Australian Sawflies.
Australia. For they can include no forms but such as have
succeeded in maintaining themselves while passing gradually
southwards through climates and surroundings which
differed at every stage in the journey, and as have found
everywhere a vegetation suitable for their ovipositions, and
held their own against a continual succession of fresh com-
petitors and enemies of all kinds. And even among such
Holarctic forms as possess this more or less exceptional
adaptability, so that they now extend into districts lying
as far south as Notogaea, probably a few only had reached
the parts of Asia adjacent to Australia when the latter
became inaccessible by its isolation. Had that isolation
been a little longer delayed, Australia might probably have
received from Arctogaea both Sawflies (e. g. Athalia and
Stromboceros) and Mammals (e.g. Tapirus and Elephas)
which seem never to have actually reached it. It is also
not surprising that the type of Sawfly (* TENTHREDO anten-
nis filiformibus : articulis 7-9°> of Linné) which is most
dominant of all in Holarctic districts—no doubt because it
is best adapted to their special surroundings—should be
precisely that which is most conspicuously absent from
Notogaea, or, at any rate, from Australia. Whereas groups
which have amore cosmopolitan range (Arginae, Lophyrinae,
and Cimbicinae) though not unrepresented in Arctogaea
form comparatively a very small part * of its Fauna.
I will now enumerate some of the most definite ways in
which Australian forms differ often or always from the
most normal Arctogaeic Sawflies. Not all the characters
to which attention will be called are invariable in Australia
or Arctogaea as the case may be; but some really are so,
when we take them one by one; and others are combined
together in one Realm in a way to which we cannot find
parallels in the other. Considered as a whole they help
to show, what has already been shown often and perhaps
more conclusively by other kinds of evidence, (1) that the
Fauna of Australia is as distinct as we should expect it to be
from its lone isolation, (2) that it mcludes representatives
of only a few of the groups occurring elsewhere, (3) and
that, however the fact is to be explained, there is more
appearance of affinity between certain Neogaeic and Noto-
* A rough calculation, based chiefly on localities cited by Konow
in Genera Insectorum, gives us in Arctogaea 4 Arginae only out of
nearly 100 genera peculiar to it, in Neogaea 16 out of 33, and in
Notogaea 3 out of 15.
Rev. F. D. Morice’s Notes on Australian Sawflies. 323
gaeic forms than between the latter and any now to be
found in Arctogaea.
As to “larval” characters, we have seen that occasion-
ally in Australia, but never in Arctogaea, forms which
feed moving freely about over their food-plants have
notw ithstanding developed no pro-legs. It would be in-
teresting to know whether rany such cases occur in Neogaea,
and especially if there are any among such genera as in other
ways seem to show affinity with Perga, ete. But I have
sought in vain to get any information on. this point, so we
may pass on at once to consider the characters of imagines.
. ) Venation of the fore-wing.
In most groups of Arctogaeic Sawflies, and in almost
all those which may be considered typical and dominant
in that Realm, the radial cell is divided by a transverse
nerve. The exceptions are the Arginae, the Lophyrinae,
and a great majority of the Nematinae.
On the contrary in Notogaeic forms, to whatever group
they may belong, the radial cell is invariably undivided. In
some cases this is not surprising, for three of the Australian
genera are Arginae, and others appear to be more akin
to that group and probably also to the Lophyrinae than to
any Arctogaeic genus in which the radial cell is divided.
But we cannot thus account for the absence of a transverse
nerve in the Syzygonides (Perga, etc.). The only existing
Arctogaeic Family in which these could possibly ‘be placed
is that of the Cimbicinae, and all Arctogaeic genera of that
Family have the radial cell divided. Such at least is now
the case though it is not easy to explain why it should be
so, for the earlier (fossil) genera of Cimbicinae—the Phena-
copergint of Rohwer’s Classification—are stated to have
the cell undivided, so that—contrary to what might have
been expected—the venation of modern Cimbex, Abia,
Amasis, ete. seems to be more “ generalised’ than that
of their probable ancestors. But it 1s possible, no doubt,
that the Syzygonids and Phenacopergini represent one
branch of the Cimbicinae in which the “ transverse radial
nerve ” long ago disappeared, and the Arctogaeie Cimbicinae
another branch of the same stock which have retained it.
However, in any case, the universal absence of this nerve
in Notogaeic Tenthredinidae is a circumstance which
Cee to be noted.
i. A character which separates all Arctogaeic Saw she
fn Hymenoptera of other Orders is the presence of <
324 Rev. F. D. Morice’s Notes on Australian Sawflies.
“lanceolate cell.” The vein which bounds this “ cell”
inferiorly, called by Konow the “ humerus,’ and by
Comstock reckoned as a branch (or branches) of the “anal
vein,” is subject to much modification. It may be visible
as running without a break from end to end of the lanceolate
cell, and keeping entirely clear of the so-called “ brachius” *
(sic! in Konow’s nomenclature) which bounds that cell
from above. Or it may seem that these veins are in part
combined into a single vein, with the result that the
lanceolate cell becomes either “Jongly contracted,” or
“petiolate.” But in no case is a lanceolate cell actually
wanting.
But in several Australian genera, belonging to at least
two or three distinct groups, no lanceolate cell whatever
can be recognised. And of the genera which possess
such a cell, one only—viz. Zenarge, “Rohwer—has the cell
shaped as in the most typical Arctogaeic genera (Dolerus,
Allantus, Tenthredella, etc., ete. In “all the others which
belong to the Arginae it is “ contracted,” and in all which
are not Arginae it is “ petiolate.” Here again, we find
an agreement between the Notogaeic and Neogaeic Faunas.
For, in Neogaea also, the lanceolate cell is wanting in
several groups, and ‘when present, is generally either
petiolate, or contracted. And here, again, the facts seem
rather puzzling. For the latest authorities on such subjects
assure US that the venation of Hymenoptera becomes
“specialised ” by Reduction (i.e. loss of veins) only !
And from this it would seem to follow that in this case
the present Arctogaeic Sawflies, which have all retained
the “vena humeralis,” are more “generalised” and
primitive than Perga, Syzygonia, and the other genera
which have lost it. Yet, if this and the other abnormal
characters of the latter were inherited from very ancient
common ancestors—and this seems more likely than that
they should have been differentiated independently and
yet identically in some half-dozen different genera in two
very distant Regions, and in no genus at all anywhere
else—it is rather surprising that those ancestors should
have had a venation less “* generalised’ and primitive
than that now universal in Arctogaea.
* Who invented this word I do not know. The nearest approach
to it I can find in Lewis and Short’s Latin Dictionary is the neuter
substantive ‘‘bracchium” (less correctly “brachium”) with an
adjective ‘‘bracchialis’’ formed from it.
Rev. F. D. Morice’s Notes on Australian Sawflies. 325
(b) Venation of the hind-wing—In most Arctogaeic
genera a “cubital” and also a “recurrent” nerve are
present in the hind-wing, and the former lies beyond the
latter (7. e. approaches nearer to the apex of the wine),
so that two “ enclosed cells” appear, of which the upper
one is larger than the lower. More rarely the recurrent
nerve only is present; and in some cases both nerves are
wanting, so that the wing has no enclosed cells at all.
In acta all indigenous genera except two out of its
three Arginae, viz. Trichorhachus and Antargidium, have
the cubital nerve present, and the recurrent absent—the
one state of things which, if I mistake not, is never to be
found in Arctogaeic forms. And both Trichorhachus and
Antargidium differ from very nearly all Arctogaeic genera,
even from their nearest relations among the Arginae, in
that, though a cubital and a recurrent nerve are present,
the former never lies beyond the latter, but (vice versa) the
recurrent nerve in Trichorhachus lies far beyond the cubital,
making the upper of the two “ cells” by far the smaller !,
while in Antargidium the two nerves are practically inter-
stitial, and the “cells” are approximately equal. I had
almost said that no Arctogaeic genus had a similar venation,
but I should have been wrong, for one has it, viz. Athalia !
There, too, the nerves are interstitial, and the two cells ,
approximately equal. Of the Neogaeic genera Syzygonia
and Incalia only seem to have a Notogaeic type of neura-
tion in the hind-wine. In other cases fwo closed cells are
regularly present, and these have the shapes and proportions
usual in Arctogaeic forms.
(c) Antennae.—The type of antenna which is beyond
all comparison the most usual in Arctogaeic Sawflies—
namely, nine nearly simple cylindrical joints, generally
tapering slightly from the base to the apex, none of them
showing any very noticeable tendency to swell out or
project at its apex and so give the antenna a “ serrate,”
‘monihate,” or “ pectinate’ appearance—seems to be
entirely unrepresented in Australia. Instead, we find
there all the Tenthredinid genera furnished with antennae
more or less resembling those of some or other Arcto-
gaeic, but not specially Arctogaeic, group. Zenarge and
Antargidium have them much as in Arge; Trichorhachus
as in Schizocera; Perga and Xyloperga as in Cimbex or
more often as in Abia; Plerygophorus and Polyclonus as
in certain Lophyrinae; and both sexes of several genera as
326 Rev. F. D. Monice’s Noles on Australian Sawflies.
in QQ (not 33) of the latter group. Nine, instead of being
the normal number of their joints, is about the rarest of
all; almost confined to one genus, Hurys, and even there
by no means universal, while the form of the joints is never
simply cylindrical.
The most characteristic of the Neogaeic Genera resemble
one or other of the Australian groups in their antennal
characters. But genera also occur there which seem to
have arrived more recently, either identical with present
Arctogaeic groups or very closely related to them, and in
these the antennae are of the prevailing Arctogaeic Type.
(d) Mouth-parts. The palpi.—Having examined dissec-
tions of the mouth-parts in many Arctogaeic Tenthredinidae
I have invariably found that the maxillary palpi had
6 joints and the labial 4. The same numbers are normal in
other Hymenopterous groups, though there are exceptions,
e.g. the Bees.
But this rule is by no means so universal either in
Notogaea or Neogaea. Citing only cases where I have
my self examined the dissections, I can testify that in the
Australian genera Phylacteophaga, Philomastix and Perga
—not, however, in Xyloperga—and in the Neogaeic Lncalia
(hirticornis), Pachylosticta (= Plagvocera) albiventris, and
. Lophyroides (= Perreyia, Auctt. nec? Brullé) tropiceus
the numbers of joints are not 6 and 4 respectively, but
4and3. Again in Syzygonia they are 5 and 3, and in what
I take to be the real Perreyia, Brullé, actually only 2 (or
possibly 3) and. I.
There is no doubt that two or more quite unrelated
groups might independently undergo a similar modifica-
tion of their mouth- -parts, and again that groups very
nearly related might differ in this character, through
adaptation to some special circumstance connected with
their feeding. (Mr. Turner has thus explained a difference
in the development of their palpi between the American
and Australian Thynnidae.)
But it seems highly improbable that the agreement in
so unusual a character between certain particular groups
in two very distant districts, these groups having also a
singular affinity in other quite different characters, should
be a mere coincidence, the American and Australian forms
having (as Cameron suggests) developed the reduction in
the number of these joints independently since they
reached their present habitats. I should suspect rather
‘ a = A . - -* ve
7 ’ , ~ 7 -
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Gags SIR ia) 1h Ce © MN reel Sites jh '
. maheles vfs
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Lay r _ Wee fe i hws if Sk) AS sar:
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bs Te : : iS ling-y Wayedisy ie. av ie
Pr Hat) oe | Oat Pro. 6 arog evento:
may ef = We ot Yo ome mmemieings add gaol
44, heer ay ie oT «, Thea Oy | : i vt d ond th)
- wep ear Le JOG, +4 Mey, +) ‘hig ij bithss4 di 2s enor
we Tye we te Mi Godt beth Wore wrad I
teas <at | Sani lh sd bin tenors
dg fe Gitte aneltyamiary A pulse
rad §
Westwood Bequest. Trans. Ent. Soc. Lond., 1918, Plate XJ.
André, Sleigh & Anglo, Lid.
Photo, F. D. Morice.
AUSTRALIAN SAWFLIES.
Fig.
EXPLANATION OF Puate XI.
Wings of Ophrynopus sericatus, &.
99
99
A
”° 29 Os
Zenarge turnert.
Hind-wing of Antargidium apicale.
Hair-patch (androconia?) on fore-wing of Perga polita, 3,
slightly magnified.
Hairs from same, magnified (4 in. power).
One of the hairs more highly magnified (4 in. power).
Wings of Phylacteophaga eucalypti.
Perga castanea, 3, showing hair-patches on both wings of
each pair.
Wings of Diphamorphos minor.
.)
Neoeurys sp. ( ?).
Hurys laetus.
Clarissa divergens.
Pterygophorus uniformis.
Philomastix nancarrowi?.
les, 1,
bo
CUES oe
Seo Ace
— = =e
ee er)
. 5 :
_—
on
16.
_—_— —
eo)
19:
EXPLANATION OF PLATE XII.
Antenna of Ophrynopus sericatus, 3.
9? 99 99 Sh
35 Trichorhachus nitidus, 3.
$5 Zenarge turneri, 3.
a Philomastix nancarrowt, 3.
” ” ” 2.
- Phylacteophaga eucalypti, 3.
5 Pterygophorus uniformis, 3.
> + 5s OF
3 % analis, ° (!).
33 Diphamorphos minor, &.
. Mouth-parts (palpi, ete.) of Perga dorsalis.
oo - » jerruginea.
Pe as Xyloperga univittata.
5 io Philomastix nancarroui.
. Phylacteophaga eucalypti.
” = Pterygophorus uniformis.
. Hind tibia of Ophrynopus sericatus, 9.
Middle ,, Zenarge turnert, &.
Westwood Bequest. Trans. Ent, Soc. Lond., 1918, Plate XII.
Photo, F. D. Morice. André, Sleigh & Anglo, Lid.
AUSTRALIAN SAWFLIES.
oo, Va a
Westwood Bequest.
r
Trans, Ent. Soc, Lond., 1918, Plate XIII.
Photo, F. D. Morice. André, Sleigh & Anglo, Tan
AUSTRALIAN SAWFLIES.
Fia.
EXPLANATION OF PLATE XIII.
1. Terebra of Ophrynopus sericatus, &.
2. Apex of ss 2 more highly magnified.
3 = HF still further magnified.
4. “Saw” and “support ” of Perga castanea.
5: an _ » gravenhorstit.
6. “Saw ” of Xyloperga univittata.
7. Support of he a
8. Saw and support of Zenarge turneri.
i). a 5 Philomastix nancarrowi.
10. e e Phylacteophaga eucalypti.
11. 93 " Pterygophorus uniformis.
12. ze 53 Clarissa divergens.
Tes 55 - Diphamorphos minor.
EXPLANATION OF PLATE XIV.
Fie. 1. Details of “saw” in Perga dorsalis.
29
affinis.
agnata.
klugit.
kirbii.
schiddtei.
intricans.
brevitarsis.
polila.
castanea.
esenbeckii.
walkeri.
lewisit.
Jerruginea.
guerinit (= smithii).
antiope.
belinda.
cameronii.
Westwood Bequest. Trans. Ent. Soc. Lond., 1918, Plate XIV.
16
Photo, F. D. Morice. André, Sleigh & Anglo, Ltd.
AUSTRALIAN SAWFLIES.
EXPLANATION OF PLATE XV.
Fra. 1. Details of “saw ” in Perga vacillans.
2 4 * » latreillei.
3h % % » spinolae.
4 p » glabra.
iss Be es », bella.
6. e e . 'divaricata”’’ (= praecedens? ).
ie x 5 » rubripes.
8. * » hartigii.
Y, 33 0 » gravenhorstii.
10. 33 35 » bicolor.
LI. 55 5 NXyloperga halidaii.
12. . _ 5 aurulenta.
Le sf a 3 univittata.
14. Third cubital cell in Perga dorsalis.
15. . 33 Xyloperga univittata.
16. Genital armature of Perga antiope, 3.
17. Larva of Perga sp. (probably dorsalis).
18. Antenna of Perga mayrii.
19. Hind tibia and tarsi of Perga antiopa, °&.
20. Antenna of Perga cameronii, 2 (4 apical joints).
(14, 15, 18 and 20 are photographed from drawings made by the
writer from specimens in B.M.)
Westwood Bequest. Trans. Ent. Soc. Lond., 1918, Plate XV.
Photo, F. D. Morice André, Sleigh & Anglo, Ltd.
AUSTRALIAN SAWFLIES.
Rev. F. D. Morice’s Notes on Australian Sawflies. 327
that in both cases the peculiarity was inherited from
Arctogaeic ancestors common to both groups, who have
bequeathed it to some, but not to all, of their descendants.
However explained, it seems a curious fact that Perga and
Xyloperga spp. (at least in all such specimens as I have
been able to examine) should differ in this character, for
apart from it the two genera are so closely allied that
it may be doubted whether we do right in separating
them.
I think that we must consider the 6- and 4-jointed con-
dition to be the primitive one, but that it is useless to spend
much thought on the question, why such and such forms
have departed from it. Had the modification anything
to do with any peculiarity in the feeding-habits of such
genera as possess it, 1t would have surely extended to
Xyloperga as well as Perga. At that we may be content
to leave it !
(e) The spinose tibiae of so many Australian imagines
are a character which is not easily accounted for. It is
an extremely rare character in Arctogaea: in fact, apart
from the Pamphilinae, it seems to be limited in the Holarctic
region to one genus, namely Avge. In Notogaea, however,
besides occurring (as might be expected) in the three
genera which are manifestly Arginae, it is found also
in Perga, Xyloperga, Phylacteophaga, Philomastix, and
Cerealces. In Neogaea, again setting aside genera of
Arginae, tibial spines (apart from the apical “ calearia,”
are found in Syzygonia and Incalia which are in other
characters closely allied to Perga and Cerealces, but not in
Pachylosticta (which is in many ways a Perga-like form).
Tibial spines occur also in several genera belonging to
eroups which, as Mr. Rohwer has lately suggested (Ann.
and Mag. Nat. Hist., November 1918), may probably be
allied to the Arginae, and also to the Australian Pterygo-
phorus. But I do not think that so large a proportion of
Neogaeic, as of Notogaeic genera possess them. Nor do
I at present feel able to draw any particular inferences
from these facts as to special affinities between Notogaeic
and Neogaeic groups unless (e.g. those which Konow calls
Syzygoniides) they agree in a considerable ageregate of
other characters.
It may be remarked that. spinose armature of the legs
is a very frequent character in Hymenoptera other than
Sawflies, and serves among these many purposes (e.g. in
TRANS. ENT. SOC. LOND. 1918.—PARTSIII,IV. (MAR, 19) z
328 Rev. F. D. Morice’s Notes on Australian Sawflies.
the pairing of the sexes, and the nidifications of sand-
burrowing Fossors) which it certainly never serves in the
case of a Sawfly. In fact, Secondary Sexual characters—
even those of the antennae—are rather noticeably infrequent
in that group, nor have any of its genera Fossorial habits.
What use they can have for tibial spines, unless, like the
calcaria, as an assistance to their “ toilettes,” I cannot
suggest. Nor can I see any reason for their more frequent
development in one group, or one district, than in
another.
As to the Stricidae and Oryssidae recorded from Weer
little need here be said of them. They amount only to 3
species in all, one of which (a Szrex) is a manifest importa-
tion. The others, though neither species is known to occur
elsewhere, belong to genera whose species are widely and
in one case very “irregularly distributed, namely, Xiphydria
(a Siricid) and Ophrynopus (an Oryssid). Xiphydria occurs
all over the world, England included, and a section of it,
to which the Australian species appears to belong, with
certain local peculiarities (unusually short ovipositor, etc.),
is represented by several species in the Oriental Region,
from which Australia in all probability received it, but
when, or how, can only be conjectured. Ophrynopus has
an extraordinarily discontinuous distribution. The metro-
polis of the genus seems to be in Neogaea, outside of which
Realm, so far as I know, it has only occurred on two
occasions (once in considerable numbers) in North Queens-
land, and also in New South Wales and in the Aru Islands
(between Australia and New Guinea). There is the closest
possible resemblance between its various species, and it
seems impossible to form any plausible theory to account
for its actual distribution. [It is remarkable that most
of the North-Queensland specimens were taken in company
with many other insects of various kinds, and that among
these were examples of an Australian Fossorial-wasp
(Aphelotoma striaticollis, Turner), of which it might almost
be supposed to bea mimic! * The district is so wild, and as
yet so little in touch with civilisation, that the insect can
hardly be thought to have been imported. Yet if it be
truly a long-established indigene, its agreement—in fact
almost identity—-with Neogaeic forms seems altogether
inexplicable !]
* The 2 also, when its wings are closed, has quite a startling
resemblance to the formidable stinging ° of a Mutilla.
Rev. F. D. Morice’s Notes on Australian Sawflies. 329
Note 4.—Proposals to break up the Genus Perga as defined
by Leach.
When Leach (1817) established the genus Perga he
described it as “Genus artificiosum, sedulose ” (sic !)
“elaborandum.” He suggested, however, no names for
the groups into which he thought it divisible, and this is
not to be regretted, for such differences between them as
he noticed are all either sexual characters, or due to
aberration in individuals. Westwood (1880), recognising
this, deliberately ignored Leach’s divisions, nor did he
himself propose any others, but confined himself to elucidat-
ing by descriptions and figures all the species with which
he was acquainted, Two years later W. F. Kirby published
his British Museum list of all Sawflies known to him by
autopsy or in literature, arranging the Perga spp. into
3 “sections ” according to differences in their anteanae,
but he gave no names to these sections, and in his later
publications I believe that he never alludes to them. Up
to that time, except Leach himself, and Lepeletier, who
quotes Leach’s remark to that effect, no author seems to
have thought the genus in need as a whole of revision,
though it was sugcested by Guérin in 1845 that it might be
desirable in future to treat two forms (P. lewisii and
ventralis—which are probably only the sexes of one species)
as a distinct subgenus, in which case he proposed to name
it Pseudoperga. There is no doubt, I think, that if i+
should become advisable to divide Perga into a number
of named sections Pseudoperga, Guérin, with lewisii,
Westw., for its Type will have to be one of them. But I
see no need for this at present, and the section, whenever
it has to be established, must be established on other
characters than that by which Guérin proposed to dis-
tinguish it, namely, the absence of a Ist cubital nerve in
the fore-wing. For (1) this nerve is not unfrequently
absent in other groups. In fact, Leach and Ashmead
describe it as absent in polita; and sometimes (though
only as an aberration) it 7s so in that, and several other
species. (2) It is, sometimes at least, quite well developed
in lewis. (3) And it is more often present than not in
ferruginea, which seems to me clearly a member of the
lewisti group.
Of the “ New Classification of the Genus Perga”’ pro-
330 Rev. F. D. Morice’s Notes on Australian Sawflies.
posed by Shipp in the Hntomologist, Dec. 1894, I have
already expressed my opinion (supra, pp. 264, 271). Much
of it is sheer nonsense, as for instance when he sets up an
altogether imaginary genus Plagioperga (characterised as
having 7 jointed antennae and 3 cubital cells), selects as
its Type precisely the one species of Leach’s genus (viz.
mayrii, Westw.) in which the antennae have not even the
usual 6 joints, but only 5 (!), and mentions as another
example of it a species really belonging to an entirely
different group—in fact, a perfectly normal Xyloperga |
There was really no excuse for his blunder about mayrit,
for Westwood not only describes but figures its 5-jointed
antennae! In one case, however, Shipp has proposed a
name which must apparently be accepted, for his “* Xylo-
perga” (n.g. with Type halidav, Westw.) happens, though
he did not “know this, to be a real natural division of the
eroup, separated from all others not by antennal characters
only, but by a different number of joints in its palpi. It
may also become necessary at some future time to accept
the restriction of the name Perga to a group with dorsalis
for its Type. Cameroni again—the Type of Shipp’s
Acanthoperga—has some very extraordinary characters,
though I doubt if they need exclude it from Perga as we
now define that genus. For Pseudoperga (with Type
lewisit) not Shipp, but Guérin is responsible. Pergadopsis
(Type dahlbomi) and Camptoperga (Type cressoniz) are
separated only by one character. Pergadopsis being said
to have 3 cubital cells only, and Camptoperga 4. This
character in my opinion is quite valueless for systematic
purposes unless it be accompanied by other differences in
the forms to be separated. However, I have examined
Westwood’s Types of dahlbomi and cressonii and can find
no such difference in the neuration as has been stated to
exist. Both appear to me to have four cubital cells, and
I see no reason to doubt that they are congeneric. Having
thus gone once more point by point over Shipp’s “ New
Classification’ I remain unconvinced that it ought to be
taken seriously.
Ashmead (1898), probably unaware that Shipp had
anticipated him, also attempted to disintegrate Leach’s
unfortunate genus. He proposed to make of it four
genera—Perga, Pseudoperga, Paraperga, and Neoperga.
Of Perga he named no Type; his Pseudoperga (Type polita)
is a * homonym”’ of Guérin’s Pseudoperga (Type lewisi) ;
Rev. F. D. Morice’s Notes on Australian Sawflies. 351
Paraperga (Type jucunda), and Neoperga (Type amenaida),
are “ synonyms” of Xyloperga, Shipp !
Konow in his unfinished Monograph, and also in Genera
Insectorum, divides the group into two genera, viz. Perga
and Heptacola. The latter name must sink as a synonym
of Xyloperga; and the author also fell into a mistake by
commencing his list of Heptacola spp. with macleayi,
Westw. That species, as I have remarked elsewhere, 1s
really a Philomastiz.
In concluding these remarks, I would suggest that,
even when a genus can be divided into more or less definite
sections, it does not follow that it is well to name such
sections, and still less to erect them into “ Genera.” The
study of any natural group is, no doubt, advanced in one
direction if we can detect and point out unnoticed differ-
ences between the sections into which (like all other natura!
eroups) it is divisible. But in another direction it is
impeded, if such stress is laid on these differences as to make
us forget the not less important differences which separate
the group as a whole from other groups. If the object of
Systematics were merely to facilitate the naming of speci-
mens, it would be only a question of practical convenience
in each case, whether at such and such a time this or that
genus should be upheld or disintegrated. But, if our
ideal be rather a classification corresponding as nearly as
our knowledge permits to the actual proportion of likeness
as well as of unlikeness existing between the objects we
are studying, I venture to think that, whereas a single
character may suftice to isolate some one form as a “ good
species,’ > much more than this—in fact, a considerable
ageregate of characters peculiar to some one section of a
eTroup (and also some reason for considering them possessed
of phylogenetic significance), should be producible, before
we are justified in treating that section as a “Genus.” It
is true that we can never hope to establish categories of
classification which shall fully: represent the desrees of
consanguinity between related organisms. But still that
should be the ideal at which we aim, and if we aim at it,
we shall hesitate before we decide to call that a generic
difference which can scarcely be distinguished from another
which we call specific.
332 Rev. F. D. Morice’s Notes on Australian Sawflies.
Note 5.—BIBLIOGRAPHICAL.
References to authors and passages cited in these Notes. Names
of Genera first recorded from Australia follow the dates between
square brackets. Synonyms and misidentifications in smaller
capitals. Genera not peculiar to Australia in italic capital letters.
Klug (Mag. Ges. nat. Fr. Berlin, VI, 4, pp. 277-280), 1812/14
[PTERYGOPHORUS].
Leach (Zool. Misc., Vol. III, pp. 115-119), 1817 [PERGA].
Westwood (Trans. Ent. Soc., p. 234), 1836.
Davis (Hntomologist, Vol. I, p. 89), 1841.
Newman (Hntomologist, Vol. I, p. 90), 1841 [KURYS].
Westwood (Arcana Entom., I, p. 24), 1841 [Dictrynna =
Kurys, supra].
Guérin (Icon. Regn. Anim., VII, p. 398), 1845 [PsEubo-
PERGA, Subgenus of PERGa].
Bennet and Scott (Proc. Zool. Soc., pp. 209-212), 1859.
Westwood (Proc. Zool. Soc., pp. 359-379), 1880.
Kirby, W. F. (Trans. Ent. Soc., p. 50), 1881 [Mowosrrcra
(antipoda = CALIROA limacina. Described from
New Zealand, but is also found in Australia. An
importation !}.
ud. (Brit. Mus. List of Hym., Vol. I), 1882
[CEREALCES, TRICHORHACHUS, EURYOPSIS
(= Evrys ¢?) POLYCLONUS, and SIREX. The
last an importation !].
Froggatt (Proc. Linn. Soc., N. S. Wales, pp. 283 and 487),
1890 [PHILOMASTIX].
Kirby, W. F. (Ann. and Mag. Nat. Hist., pp. 38-43), 1893.
id. (id., pp. 45-57), 1894 [CLARISSA and
Hytoroma (= ANTARGIDIUM)].
Shipp (Entomologist, pp. 338-340), 1894 [XYLOPERGA
(and other “ Genera’? which I do not recognise as
such) |.
Frogeatt (Proc. Linn. Soc., N. S. Wales, p. 131), 1899
[PHY LACTEOPHAGA].
Moesary (Term. Fuz., V, 23), 1900 [OPHRYNOPUS].
Turner, Gilbert (Proc. Linn. Soc., N.S. Wales, pp. 514, 518),
1900 [Oryssus, 7. e. OPHRYNOPUS, supra}.
Konow (Syst. Zus. der Chalast. in Zeitschr. f. Hym. u. Dopt.,
1901-1908).
id. (Lenthredinidae, in Genera Insectorum), 1905
| HepracoLa = XYLOPERGA, supra].
Rev. F. D. Morice’s Notes on Australian Sawflies. 333
Konow (Zeitschr. f. Hym. u. Dipt.—Plerygophorus), 1907.
Rohwer (nt. News, Philadelphia, pp. 457 et seq.), 1910
[NEOEURYS, DIPHAMORPHOS].
ul. (Ann. and Mag. Nat. Hist., November), 1918
[XIPHY DRIA, ZENARGE].
Vide also “ Australian Insects,’ by W. W. Froggatt
(Sydney), 1907.
EXPLANATION OF PLratEes XI—XV.
(See Explanation facing the PLatRs. |
XV. The Hymenoptera of Fiji. By Rowianp E. Turner,
F.Z8., FES.
[Read November 20th, 1918.]
ONnty fifty-three Hymenoptera seem so far to have been
recorded from Fiji, including five new species described
here. Of these several are undoubtedly introduced
species, and others are known to have a wide range in
Polynesia. A few of the larger species are almost certainly
confined to Fiji, and show no near relationship to species
found in any other group of islands. Thus Cyphononyx
vitiensis, Turn., is very distinct from any of the Psam-
mocharidae inhabiting New Caledonia or New Zealand;
and Stizus inermis, Handl., i is very distinct in the structure
of the male antennae from the wide-ranging section of the
genus to which it approaches most nearly in other respects.
Though doubtless the fauna of the group is very poor in
the larger Hymenoptera, there must be many of the more
minute, species still remaining to be discovered, and it is
important that the fauna should be studied before it
becomes too much changed by the ravages of cultivation
and the competition of imported forms.
Most of the material used for this paper was collected
by Mr. R. Veitch and forwarded to the Imperial Bureau
of Entomology.
Family FORMICIDAE.
Subfamily PONERINAE.
1. Odontomachus angulatus, Mayr.
Odontomachus angulatus, Mayr, Sitzungsber. Akad. Wiss.
Wien, ln, p. 500, 1866.
Hab. Ovalau.
Qdontomachus haematoda, Linn.
Formica haematoda, Linn., Syst. nat. Ed. 10, 1, p. 582,
1758.
Odontomachus haematodes, Latr., Hist. nat. Crust. et Insect,
XL eps ons
TRANS. ENT. SOC. LOND. 1918.—PARTS II, IV. (MAR.’19)
Mr. Rowland E. Turner on the Hymenoptera of Fiji. 335
Hab. Natova (R. Veitch), August; Nairai (Voyage of
the Herald), November 1855. Also from almost all tropical
regions.
Subfamily MYRMECINAE.
3. Cardiocondyla nuda, Mayr.
Leptothorax nudus, Mayr, Sitzungsber. Akad. Wiss. Wien,
lai, p. 508, 1866.
Cardiocondyla nuda, Forel, Mitth. Miinchen. Entom. Ver.,
Ve «d lool
A wide-ranging species in the Oriental and Australian
regions. .
4. Pheidole oceanica, Mayr.
Pheidole oceanica, Mayr, Sitzungsber. Akad. Wiss. Wien,
ln, p. 510, 1866, 2 2/ (nec 9, nec 9g).
Hab. Ovalau. Also from Tonga.
5. Pheidole umbonata, Mayr.
Pheidole oceanica, Mayr, Sitzungsber. Akad. Wiss. Wien,
tun, p. 510, 1866, Sg (nec 9 nec Y).
Pheidole umbonata, Mayr, Verh. Zool.-bot. Ges. Wien, xx,
DRO Ole 2).
Hab. Ovalau. Also from Tonga.
Subfamily C4 MPONOTINAE.
6. Camponotus cristatus, Mayr.
Camponotus cristatus, Mayr, Sitzungsber. Akad. Wiss.
Wien, lin, p. 489, 1866.
Hab. Ovalau.
7. Camponotus laminatus, Mayr.
Camponotus laminatus, Mayr, Sitzungsber. Akad. Wiss.
Wien, li, p. 489, 1866.
Hab. Ovalau.
8. Camponotus schmeltzii, Mayr.
Camponotus schmeltzii, Mayr, Sitzungsber. Akad. Wiss.
Wien, liu, p. 490, 1866.
Hab. Ovalau.
336 Mr. Row and E. Turner on
9. Camponotus (Colobopsis) dentatus, Mayr.
Colobopsis dentata, Mayr, Sitzunesber. Akad. Wiss. Wien,
hn, p. 492, 1866.
Hab, Ovalau.
10. Camponotus (Colobopsis) carinatus, Mayr.
Colobopsis carinata, Mayr, Verh. Zool.-bot. Ges. Wien, xx,
p. 948, 1870.
Hab. Ovalau.
11. Camponotus (Colobopsis) oceanicus, Mayr.
Colobopsis oceanica, Mayr, Verh. Zool.-bot. Ges. Wien, xx,
p. 948, 1870.
Hab. Ovalau.
Family APIDAE.
Subfamily PROSOPIDINAE.
12. Prosopis fijiensis, Ckll.
Prosopis fijiensis, Ckll., Ann. & Mag. Nat. Hist. (8) iv,
p. 993, 1909, 9.
I think this species should be placed in the genus Palaeo-
rhiza, Pkns., but, as IT have only seen the female, I leave
it provisionally in Prosopis.
Subfamily ANDRENINAE.
13. Halie‘us perpessicius, Kohl.
Halictus perpessicius, Kohl, Denkschr. Akad. Wiss. Wien,
Ixxxi, p. 307, 1908, Q¢.
Hab. Cuvu (R. Veitch), June. Described from Samoa,
but also recorded from Fiji by Kohl.
Subfamily MEGACHILINAE.
14. Lithurgus albofimbriatus, Sichel.
Lithurgqus albofimbriatus, Sichel, Reise d. Novara Zool. ii,
Hymen., p. 154, 1867, 9.
Hab. Cuvu (R. Veitch), July and August. Also from
Tahiti.
This species has recently become established in Hawaii.
the Hymenoptera of Fiji. 337
15. Megachile scutellata, Sm.
Megachile scutellata, Sm., Deser. New Spec. Hymen.,
p. 66, 1879, 2
Hab. Cuvu (R. Veitch), June.
16. Megachile fimbriventris, riese.
Megachile fimbriventris, Friese, Deutsche Ent. Zeitschr.,
p. 493, 1911.
Hab. Cuvu (R. Veitch), June.
This seems to me to be a subspecies of M. similis, Sm.,
from the New Hebrides, differing in the distinctly stronger
puncturation of the tergites.
Family SPHEGIDAE.
Subfamily STJZINAE.
17. Stizus inermis, Handl.
Stizus inermis, Handl., Sitzungsb., Akad. Wiss. Wien, ci,
p. 91, 1892, 3.
Stizus pacificus, Turn., Trans. Ent. Soc. London, p. 82,
1917, 9.
The male varies very much in colour, the abdomen in
some specimens being almost entirely pale yellow, also
the greater part of the median segment and postscutellum,
the greater part of the scutellum laterally, the sides of
the mesonotum and two longitudinal bands near the
middle of the mesonotum. The colour of the female does
not seem to vary as much.
Hab. Cuvu (R. Veitch), January, $2; Natova, October, °.
Though near the tridens group, this species is very
distinct in the simple antennae of the male, as pointed out
by Handlirsch.
Subfamily CRABRONINAE.
18. Rhopalum oceanicum, Schulz.
Crabro (Rhopalum) oceanicus, Schulz, Spolia Hymenopt.,
p. 202, 1906.
19. Crabro veitchi, Turn.
)
Crabro veitchi, Turn., Trans. Ent. Soe. London, p. 84,
191i, 2.
338 Mr. Rowland E. Turner on
Subfamily LARRINAE.
20. Notogonia retiaria, Turn.
Notogonia retiaria, Turn., Proc. Zool. Soc. London, p. 479,
1908.
Hab. Natova (R. Veitch), April; Cuvu, January. Also
from Australia.
Subfamily 7RYPOX YLONIN AE.
21. Pison ignavum, Turn.
Pison ignavum, Turn., Proc. Zool. Soc. London, p. 511,
1908.
Hab. Rarawai (R. Veitch), November. Also from
(Jueensland.
22. Pison tahitense, Sauss.
Pison tahitense, Sauss., Reise d. Novara Zool., 11, Hymen.,
p. 65, 1867.
Hab. Natova (R. Veitch), October.
Described from Tahiti, also recorded by Kohl from
Samoa.
23. Pison rechingeri, Kohl.
Pison rechingert, Kohl, Denkschr. Akad. Wiss. Wien,
Ixxoarp: 309; 1908:
Hab. Fiji (R. C. L. Perkins).
Described from Samoa.
Family EUMENIDAE.
24. Eumenes ovalauensis, Sauss.
Eumenes ovalauensis, Sauss., Stett. Entom. Zeit., xxx,
p. 53, 1869.
Belenogaster bidentatus, W. F. Kirby, Ann. & Mag. Nat.
Hist. (5) xiii, p. 410, 1884, 3.
Hab. Suva (Woodford); Sigatoka (R. Veitch), May.
25. Rhynchium rufipes, abr.
Vespa rufipes, Fabr., Syst. Ent., p. 367, 1775.
Rhynchium rufipes, Sauss., Reise d. Novara, Zool. u,
p: 3, 1667.
Hab. Cuvu (R. Veitch), September; Sigatoka, May.
Also from Rarotonga Tahiti and other Pacific Islands.
the Hymenoptera of Fiji. 339
26. Odynerus (Leionotus) mediocinctus, sp. n
2. Nigra; mandibulis, clypeo, macula inter antennas, scapo,
flagelli articulo primo, prothorace, mesopleuris macula magua sub
alis, tegulis, scutello fascia lata transversa, segmento mediano
macula apicali utrinque, segmentis abdominalibus primo, quinto
sextoque, pedibusque rufo-aurantiacis; alis infumatis, venis fuscis.
Long. 9 mm.
Q. Clypeus rather sparsely punctured, much longer than its
greatest breadth, rather narrowly subtruncate at the apex; a
short longitudinal carina between the antennae. Front strongly,
vertex more finely punctured; thorax sparsely, but rather strongly,
punctured, more finely on the pleurae than on the dorsal surface,
somewhat elongate; scutellum and postscutellum almost. flat;
the postscutellum subtriangular, narrowly rounded at the apex.
Median segment prolonged horizontally at the sides, the middle
strongly convex from the apex of the postscutellum. Abdomen
shining, with a few scattered punctures; first tergite scarcely
more than half as broad at the apex as the apex of the second, the
second somewhat constricted at the base, longer than its greatest
breadth; second sternite rather sparsely punctured, almost. flat.
Second abscissa of the radius very short, the second cubital cell
almost triangular.
HaboKui(h. Vewtch) 1-2.
It is possible that the colour of the markings has been
altered by cyanide and should be yellow, as in the allied
species, O. bizonatus, Sauss., and O. quodi, Vach., to which
it is closely allied in structure and sculpture, though
differing much in the distribution of the colour on the
abdomen.
Alastor (Paralastor ?) graeffei, Sauss.
Alastor graeffer, Sauss., Stett. Entom. Zeit.. xxx, p. 5),
1869.
Hab. Ovalau.
Family VESPIDAE.
28. Polistes maecaensis, Fabr.
Vespa macaensis, Fabr., Entom. Syst. u, p. 259, 1793.
Polistes macaensis, Fabr., Syst. Piez., >. 2 272, 1804.
This species has been imported into Fiji, and into many
other Pacific Islands.
340 Mr. Rowland E. Turner on
Family SCOLIIDAE.
Subfamily SCOLIINAE.
29. Seolia ovalauensis, Sauss.
Discolia ovalauensis, Sauss., Stett. Entom. Zeit., xxx,
p- 62, 1869, Og.
Hab. Ovalau (Saussure); Suva (Woodford); Cuvu (R.
Veitch), June to August.
Family PSAMMOCHARIDAE.
30. Cyphononyx vitiensis, Turn.
Cyphononyx vitiensis, Turn., Trans. Ent. Soc. London,
De 18, Loli es:
Hab. Rarawai (R. Veitch), October to January; Natova
(R. Veitch), October; Cuvu, (R. Veitch), May.
51. Psammochares elatus, Sm.
Pompilus elatus, Sm., Journ. Proc. Linn. Soc. Zool., viii,
p. 82, 1862.
Pompilus inquirendus, Vachal, Revue d’ Entomologie, xxiv,
(oy MUIR ALS BYE
Hab. Cuvu (R. Veitch), January. Also from Vavau,
New Caledonia, N. Queensland and Morty.
Typical elatus from Morty has the third abscissa of the
radius nearly half as long as the second, whereas in in-
quirendus, which occurs in the other localities mentioned,
the third cubital cell is pointed on the radius.
Family DRYINIDAE.
32. Haplogonatopus vitiensis, Pkns.
Haplogonatopus vitiensis, Pkns., Exp. Stat. Hawaiian Sug.
Pl. Ass. Entom. Bull., i, p. 488, 1906.
33. Pseudogonatopus melanacrias, Pkns.
Pseudogonatopus melanacrias, Pkns., Exp. Stat. Hawaiian
Sug. Pl. Ass. Entom. Bull., i, p. 487, 1906.
O4. Pseudogonatopus kiefferi, Pkns.
Pseudogonatopus kiefferi, Pkns., Exp. Stat. Hawaiian Sug.
Pl. Ass. Entom. Bull. i, p. 487, 1906.
the Hymenoptera of Fiji. B41
35. Gonatopus anomala, Pkns.
Gonalopus anomala, Pkns., Exp. Stat. Hawaian Sue. PI.
Ass. Entom. Bull. xi, p. 14, 1912.
36. Neogonatopus vitiensis, Pkns.
Neogonatopus vitiensis, Pkns., Exp. Stat. Hawatan Sue.
Pl. Ass. Entom. Bull., 1, p. 490, 1906.
Family CHALCIDIDAE.
Subfamily ENCYRTINAE.
37. Coenocyrtus pacificus, Waterst.
Ooenocyrtus pacificus, Waterst., Bull. Entom. Res., vi,
p. 307, 1915.
Subfamily APHELINAE.
38. Physeus fijiensis, Howard.
Physcus fyyvensis, Howard, Proc. Entom. Soc. Washington,
Vis. Os, OIA.
Subfamily MY MARINAE,
39. Polynema eucharis, Pkns.
Polynema eucharis, Pkns., Exp. Stat. Hawaiian Sue. Pl.
Ass. Entom. Bull., x, p. 25, 1912.
40. Dicopus psyche, Girault.
Dicopus psyche, Girault, Proc. Entom. Soc. Washington,
xvas Pp: 22, LOL:
Family EVANIIDAE.
Subfamily EVANIININAE.
41. Evania appendigaster, Linn.
Ichneumon appendigaster, Linn., Syst. Nat. Ed. 10°, i,
p. 566, 1758.
Evania appendigaster, Fabr., Syst. Ent., p. 345, 1775.
Hab. Cuvu (R. Veitch), June.
This cosmopolitan species has been spread by ships to
every part of the world.
342 Mr. Rowland E. Turner on
42. Evania impressa, Schlett.
Evania impressa, Schlett., Ann. Naturh. Hofmns. Wien,
iv, p. 153, 1889.
Hab. Natova (R. Veitch), January and June.
Also recorded from the Philippines, New Guinea, Palau
and Tonga. There is also a female from Malekula, New
Hebrides in the British Museum collection.
Subfamily FORNINAE.
43. Hyptiogaster ex‘ranea, sp. n.
3. Ferrugineus; abdomine supra, femoribus tibiisque posticis
supra, tarsis posticis flagelloque fuscis; tegulis pedibusque anticis
intermediisque flavo-testaceis; alis hyalinis, iridescentibus, venis
nigris.
Long. 7 mm.
3. Very slender; head broader than the thorax, clypeus and
face shining, closely microscopically punctured; front and vertex
opaque, very finely granulate. Second joint of the flagellum three
times as long as the first, equal to the combined length of the first
and third joints. Neck rather short; prothorax rounded, without
spines; mesonotum shorter than its apical breadth, rather strongly
transversely striated, the parapsidal furrows deep and nearly
reaching the posterior margin. Scutellum transversely striated,
strongly depressed at the apex, with strong lateral and apical
marginal carinae. Median segment convex, longer than broad,
rugulose, with one or two distinct transverse striae in the middle.
Petiole and the whole abdomen smooth and very slender, the dorsal
surface almost black, tergites 2-5 luteous at the apex; petiole as
long as the three following segments combined. Joints of the hind
tarsi symmetrical, much longer than broad, the ungues small, hind
tibiae thinly clothed with short upright hairs. Cubitus originating
just below the middle of the basal nervure.
Hab. Cuvu (R. Veitch), June.
This is allied to the Australian species H. darwini,
Westw., but is a more slender species and differs much in
the sculpture of the mesonotum, in the symmetrical joints
of the hind tarsi, and in the hairs on the hind tibiae. The
female is unknown, but doubtless belongs to the group in
which the terebra does not reach beyond the apex of the
abdomen.
the Hymenoptera of Fiji. 343
Family ICHNEUMONIDAE.
Subfamily P/MPLINAL.
44. Lissopimpla semipunctata, Kirby.
Rhyssa semipunctata, W. F. Kirby, Trans. Ent. Soc.,
London, p. 202, 1883.
Lissopimpla decemnotata, Kriechb., Entom. Nachr., xv,
p. 310, 1889.
Lissopimpla haemorrhoidalis, Kriech., Entom. Nachr., xv,
p. 310, 1889.
Lissopimpla semipunctata, Cam., Mem. Manchester Lit. &
Phil. Soc., xlvi, 1902. :
Krieger records this common Australian species from
Fiji. It is doubtless an imported species.
45. Lissopimpla veitchi, sp. n.
°. Fusco-ferruginea; facie, clypeo, pedibusque rufescentibus ;
abdomine mesonotoque obscure violaceo suffusis; antennis articulis
12-14 albidis; alis hyalinis, venis fuscis, stigmate ochraceo.
3. Feminae similis, antennis omnino fuscis, stigmate, tibiis
tarsisque fuscis, tibiis anticis infra ochraceis.
Long. 2, 7 mm.; terebrae long. 3 mm.; 3, 7
2. Basal portion of the clypeus shining and almost smooth; the
apical portion (clypeolus) finely and closely punctured, almost
black. Eyes widely and shallowly emarginate on the inner margin,
separated from the mandibles by a distance equal to about twice
the breadth of the mandibles at their base. Face finely and irregu-
larly punctured, with a broad median longitudinal carina; raised
into a broadly V-shaped carina below the base of the antennae ;
the face shallowly concave on each side of the median carina. Front
very shallowly concave from the anterior ocellus to the base of the
antennae, smooth and shining. Thorax shining almost smooth,
the mesonotum very minutely punctured, parapsidal furrows
strongly developed; scutellum with distinct marginal carinae from
the basal angles reaching to the middle of the lateral margins but
not to the apex; postscutellum shining; pleurae smooth and
shining, the longitudinal grooves on the mesopleurae less strongly
developed than in L. semipunctata. Median segment with lateral
and apical marginal carinae, and with two longitudinal carinae
near the middle running from the base to the apical carina, the two
median carinae more than twice as far from the lateral carinae as
from each other; the dorsal surface of the segment rugulose, the
apical slope oblique and almost smooth, the apical carina not
TRANS. ENT. SOC. LOND. 1918.—PARTS III, IV. (MAR.'19) AA
mim.
344 Mr. Rowland E. Turner on
produced into spines either at the apical angles or in the middle;
the lateral carinae with a rather sharp angle in the middle. Abdo-
men smooth and shining; the first segment nearly twice as long as
its apical breadth; second and third segments with a shallow
groove on each side before the apex. Hind femora with a small
tooth beneath nearly three-quarters from the base; hind tibiae
almost smooth, the spines on the outer margin microscopic. Ner-
vulus antefureal; the mediella and cubitella forming a continuous
line without an angle at their junction, the nervellus sharply bent
just before its junction with the cubitella, the discoidella originating
at the angle formed by the bend in the nervellus.
Hab. Natova, Fiji (R. Veitch), April, 1918.
In colour this resembles LZ. concolor, Krieg., from Timor,
but differs in the absence of apical spines or lamellae on
the median segment, also in sculpture and in the neuration
of the hind-wing; in the latter the mode of junction of
the mediella and cubitella shows affinity with Theronia,
but I consider that the form of the clypeus, the deep parap-
sidal furrows, the spine or tubercle on the hind femora
and. the antefurcal nervulus show conclusively that the
species belongs to Lissopimpla. The radius of the fore-wing
resembles that of Theronia, and is not sinuate beyond the
areolet as in typical Lissopimpla.
; 46, Eehthromorpha immaculata, Krieg.
Echthromorpha immaculata, Krieg., Mitt. Zool. Mus.
Berlin, iv, p. 331, 1909.
Hab. Fiji.
Species of Echthromorpha are recorded from. many of
the Pacific Islands, but I have not seen ammaculata.
47. Echthromorpha diversor, Morl.
Echthromorpha diversor, Morl., Revis. Ichneum., 11, p. 47,
1913.
Hab. Cuvu (R. Veitch), May to July; Nadi, October.
Subfamily OPHIONINAE.
48. Henicospilus turneri, Mor.
Henicospilus turneri, Morl., Revis. Ichneum., i, p. 51, 1912.
The single specimen sent by Mr. Veitch has the sculpture
of the median segment much stronger than in typical
Queensland specimens, the striae being strongly developed ;
it will probably constitute at least a subspecies.
the Hymenoptera of Fiji. 345
49, Henicospilus apicifumatus, Morl.
Henicospilus apicifumatus, Morl., Entomologist, xlvii,
p. 139, 1915.
Hab. Nadi, Nadovi and Sigatoka (R. Veitch), March and
September.
Apparently a common species.
50. Paniseus opaculus, Thoms.
Paniscus opaculus, Thoms., Opuse. Entom., p. 1199, L888.
Hab. Nadi. Also from the whole Eastern hemisphere.
Apparently identical with Queensland specimens deter-
mined by Morley.
Subfamily /¢ 'HNEUMONINAE.
51. Ichneumon (Euichneumon) promissorius, Erichs.
Ichneumon promissorius, Ervichs., Arch. f. Naturges, vil,
1, p. 206, 1841.
Probolus albocinctus, Cam., Entomologist, p. 181, 1906, ¥.
Probolus varilineatus, Cam., Proc. Linn. Soc. New South
Wales, p. 194, 1912, g.
Hab. Natova (R. Veitch), April. Also from Tasmania
and BE. Australia as far north as Mackay.
I cannot find any specific distinction between Fijian
and Australian specimens, and conclude that the species
has been recently imported into Fiji.
Family BRACONIDAE.
Subfamily CHELONINAE.
52. Chelonus vitiensis, sp. 1.
3. Niger; mandibulis, scapo, tegulis, pedibusque, coxis inclusis,
rufo-testaceis; tibiis posticis apice leviter infumatis, tarsis posticis
fuscis; palpis pallidis; alis hyalinis, iridescentibus, stigmate
venisque fuscis.
Long. 3 mm.
g. Antennae 24-jointed ; head transverse, distinctly narrowed
behind the eyes, opaque and minutely punctured. Mesonotum
closely punctured-rugulose, more coarsely posteriorly than anteriorly ;
scutellum finely punctured, with a strongly crenulate transverse
basal groove; mesopleurae coarsely punctured. Postscutellum
longitudinally striated. Median segment short, transverse, coarsely
346 Mr. Rowland E. Turner on the Hymenoptera of Fit.
reticulate, with a low carina from the base to the apex of the dorsal
surface, the posterior angles produced and armed with a short
spine; the surface of the posterior truncation finely punctured-
rugulose. Abdomen about half as long again as the thorax, rather
slender, at least four times as long as its basal breadth, not incised
at the apex; the basal half coarsely longitudinally striated, with
oblong reticulations; the third quarter finely punctured granulate,
with fine longitudinal striae at the base; the apical quarter very
closely and minutely punctured. Radial cell broad, a little shorter
on the costa than the stigma, third abscissa of the radius straight.
Hab. Cuvu (R. Veitch), September.
The colouring is somewhat similar to that of C. rufipes,
Szép., from New Guinea and E. Australa, but the antennae
in that species are testaceous almost to the apex and the
sculpture of the thorax is coarser, especially on the meso-
notum, than in the present species; there is also an apical
abdominal incision in rufipes.
Subfamily WICROGASTERINAE.
53. Apanteles expulsus, sp. n.
©. Nigra; scapo, apice excepto, palpisque luteis; flagello basi
subtus pedibusque flavo-testaceis, coxis nigris; trochanteribus
posticis supra nigris; alis hyalinis, venis luteis; stigmate fusco-
ferrugineo; terebra brevissima; segmento mediano areolato.
Long. 2mm.
©, Antennae 18-jointed. Mesonotum and pleurae finely and
closely punctured, subopaque; scutellum shining and almost
smooth. Median segment short, not as long as the scutellum,
with a smooth rhombic area in the middle from base to apex;
the sides minutely punctured. First and second tergites finely
rugose; the first tergite broad, the hind margin transverse, the
second tergite about equal to the third in length; the third and
following tergites smooth and shining. Hind coxae shining,
minutely punctured; spurs of hind tibiae slender, not more than
half as long as the metatarsus. Terebra exserted, very short.
Cocoons pure white, not enclosed in a web.
Hab. Natova (R. Veitch), April.
Bred from the larva of a Noctuid moth (Anticarsia
irrorata Fabr.). This is near the Urogaster section of the
venus, but has the terebra shorter than usual, not reaching
beyond the apical tergite.
XVI. Notes on a large Heliconine collection made in French
Guana im 1917, compared with a similar collection
made in 1915. By J. J. Joicey, F.E.S., and W. J.
Kaye, F.E.S.
[Read November 6th, 1918.]
With SKETCH Map.
PerHAPs the most striking and interesting point about
this great collection is that the percentages both as to
the various forms under melpomene and under erato, and
also the ratios of the one species to the other, are found
to be in substance the same as those worked out in our
previous paper (Trans. Ent. Soc. 1917, pp. 412-431), thus
giving confirmation to our published figures. The present
collection is four times as large as the one made in OUD,
and when shght discrepancies occur in percentages prob-
ably the present figures are more correct. Thus in 1915
the number of black hind-winged melpomene was 125 out
of (31, or 1753 o> but in the present collection there are
only 302 out of 2,935, or 10°29 %, and we think it highly
probable that the latter figure is more correct. The red
basal streaked section is near enough (54°32 %% against
57°03 °%) to practically prove that it preponderates over
the other two sections combined, while it follows that
et the black hind-winged section lost the fully streaked
“thelxiope > hind-wing gained, so that in the present
eoiecscd the fully- Bitcalced ‘section have 35°39 °% instead |
of 25°44 % in 1915.
The number of H. melpomene secured is the very large
total of 2,935. They are divided amongst the three
sections as follows :—
mel- Percentage | mel- Percentage
pomene, of Total. pomene. of Total.
Black hind-wing . |1917| 302 10-29 }1915) 125 17-53
Zed basal streak . |1917) 1,592 | 54-32 [1915| 420 57-03
Zed basal streak | 1917| 1,041 35:39 11915! 186 25-44.
and cross streaks |
2,935 | 100-00 731 100-00
Cd
"TRANS. ENT. SOC. LOND. 1918.—PaRTS III, IV. (mAn, 19)
348 Messrs. J. J. Joicey and W. J. Kaye’s Notes on
We have heard from Mons. le Moult that the collectors
have instructions not to catch typical melpomene, and that
in his own experience very many more melpomene should
be estimated for than what we did in our former paper.
It is unfortunate that any check was put on the collectors
from the scientific standpoint. The remarkable fact, how-
ever, remains that of the two collections there is very
close agreement, and that, whatever the correct propor-
tion of typical melpomene may be, the addition would be
approximately the same for- both collections. Prof.
E. B. Poulton has made the interesting observation to
me that probably the cybele type of hind-wing with the
short red streak would on the wing be much more likely
to be mistaken for the all-black hind-wing than the
thelxiope-streaked hind-wing. It is clear, if this is true,
that the fully-streaked forms are in a considerable minority
and not at all like Para, where they are practically the
only forms found.
Those forms are rarest that represent the most distant
geographical races. Thus ab. penelope occurs as a race in
Bolivia on the Rio Juntas, ab. rufolimbata is from the
Tapajos River, ab. timareta occurs as a race in Kast
Ecuador at Sta Inez and elsewhere. This last form has
not yet been seen in the French Guiana collections, but
by inference it should occur, even if very rarely, as it 1s
only the representative of penelope without any red on
fore- or hind-wing. The penelope forms graduate into
vicina forms, the latter occurring as a race on the Upper
- Amazon at Pebas and Teffe.
Several aberrations are of special interest and afford
fresh connecting links. There is one specimen of the
melpina form, which shows three yellow subapical spots.
This suggests at once the spotting of such species (or
races of melpomene) as hermogenes or galanthus. Although
we have now received in all 3,666 melpomene from
French Guiana, this is the only specimen showing such
spotting.
Three new forms, one of the cybele section and two of
the melpomene section, we think should be named as they
are representative of already named similar forms but
with different hind-wing. The first, which we call facvrer,
after Mons. Faivre, is complementary to negroida and
negroidens. A second form of the melpomene hind-wing
section which we call compacta is complementary to faustalia
a large Heliconine collection made in French Guiana. 349
and rufolimbata, while the third new form we call cybeleva,
represents aglaopera with a cybele hind-wing.
H. melpomene melpomene ab. faivrei, nov.
Fore-wing black with only a dusky yellow half-band at end of
cell, edged externally with an almost equal half-band of red. Hind-
wing wholly black.
Hab. Frence Gutana, St. Jean de Maroni.
Type in coll. Joicey.
This form is the same fore-wing form as negroida and
negroidens, but with a black hind-wing.
H. melpomene melpomene ab. compacta, nov.
Fore-wing black with a large solid yellow patch around the
discocellulars, the veins alone showing black, and with a half-band
of red edging the yellow patch externally between costa and vein 4.
Hind-wing wholly black.
Hab. Frencu Gurtana, St. Jean de Maroni.
Type in coll. Joicey.
This form is the equivalent of faustalia and rufolimbata
as to fore-wing, but with a black hind-wing.
H. melpomene cybele ab. cybeleia, nov.
Fore-wing like aglaopeia, with the yellow group of spots darkened
with blackish. Hind-wing like cybele, with the short red basal
streak.
Hab. Frencu Gurana, St. Jean de Maroni.
Type in coll. Joicey.
This is the representative of aglaopeia with a cybele
hind-wing.
It is most unfortunate that Staudinger gave the name
aglaopeia to an insect which is not a bit like aglaope.
However, as it is well figured in the ‘‘ Iris ”’ (vokax ELV),
the form he named aglaopeia need never be in doubt.
The equivalent form with a black hind-wing has not vet
been seen.
A very interesting and suggestive aberration is one of
the melanippe form showing a trace of a yellow basal
350 Messrs. J. J. Joicey and W. J. Kaye’s Notes on
streak along the median vein, thus suggesting the well-
developed yellow streak in such races as nanna from
S. Brazil, and to a lesser extent in amandus from E. Bolivia.
Many specimens of the black hind-wing section of melpo-
mene from F. Guiana show a yellow basal blotch at the
submedian, but the extension along the median seems to
be very infrequently developed.
There are one or two specimens showing white markings
partly in place of yellow, and these our friend Dr. Eltring-
ham will consider, and rightly so, as lending support to
his theory that the Colombian and Central American
white marked species cydno, galanthus and hermogenes are
really races of melpomene.
There are four specimens of different fascies all showing
a white portion of what would be the true melpomene red
patch. Thus one is nearly an aglaopeia, with what is
usually the yellow spot in the cell partly white and partly
black scaled.
Another of the cybele form has a large circular white
spot almost occupying the yellow spot ‘between veins 2
and 3. Two others approximating to the faustina form
have white, in the one occupying the yellow spaces between
veins 5, 6, and 6, 7 on one side, and on the other occupy-
ing the costal yellow spot. In the second there is white
in the right fore-wing only, within the yellow discoidal
spot and ‘within the yellow spots beyond the cell.
The very long series of erato is equally variable with
the melpomene, “and is chiefly different from the series
made in 1915 in that there are no fewer than 45 of the
tellus form, which was completely absent in the former
collection. There were 5 of the constricta form then
against 25 of the same form now, while the number of
andremona forms with a varying amount of white over-
laying pattern is much greater in the present series. One
of the erato (typical) has part of the yellow group of
spots in fore-wing white, for this form we propose the
name albida. The comparatively large number of the
tellus form emphasises what we said in our former paper,
that the streaked forms of erato are essentially the
models for melpomene, as here there are 45 of this form
against 6 melpomene ab. penelope graduating into ab.
vicinus. In both collections the percentage of streaked
forms is very high, and the present collection is a remark-
able confirmation of the deduction arrived at from the
a large Heliconine collection made in French Guiana. 351
1915 collection; for although the collection is eight times
the size the percentage of streaked and black hind-winged
forms is quite remarkably close.
The total number of H. erato, the companion species of
the second great division of Heliconius, 1s 1,123. Only
46 of this large number show a black hind-wing. In 1915
the number of black hind-wing forms was 6 out of 155.
Jey.
Per erato. Ee
erato.
centage, centage,
Black hind-wing . | 1917 46 4:10 J1915 6 3°87
|
Streaked hind-wing | 1917, 1,099 | 95:90 ]1915 149 95:97
1,123 | 100-00 155 | 100-00
It is difficult, if not nearly impossible, to get a really
just set of figures for comparing the darkened fore-wing
forms of both melpomene and erato. Melpomene in its
cybele section and its thelavope section shows completely
darkened fore-wing in the forms funebris and styguanus
respectively, but in the all-black hind-wing no wholly
blackened fore-wing form has yet occurred, this forming
a wholly black insect. In erato the form oberthueri is
the darkest known form from this region, but this shows
some slight remnant of the yellow, and there are all
eradations up to vesta. It is thus difficult to know how
many erato to include, and we fancy we really included too
many in our table given at the top of p. 429 of our former
paper. Keeping strictly to the VERY DARKEST FORE-WING
forms of both species, we get these comparisons :—
|
Species. N umbers.| Percentage Numbers. Dae
melpomene . . 917 TA, Peed PIGS 162s, 18348
Craton oe ood 1% 151 ]1915 10 | 6:45
This as a comparison between the two species Is prob-
ably approximately correct, but it is hardly right to
compare the 1915 figures, as we realise we included too
many forms which were not sufficiently extreme. The
352
Messrs. J. J. Joicey and W. J. Kaye’s Notes on
comparisons between the BLACK HIND-WING forms of the
two species are far more satisfactory.
A COMPARISON BETWEEN THE BLAck HIND-winG FORMS OF
MELPOMENE AND ERATO.
Numbers |,,. is Numbers / ,..
Species. with black pera with black | Pere
hind-wing, | EP ate tae hind-wing, | Ce Ouaee
melpomene . 1917 302 10-29 | 1915 125 17-53
erato 1917 46 4:10 | 1915 6 3°87
A COMPARISON BETWEEN THE STREAKED HIND-WING FORMS OF
MELPOMENE
AND ERATO.
Numbers Pp Rr Numbers -
Species, with streaked Ee eee with streaked | P i wae °
hind-wing,. : pe hinds wines ase
melpomene 1917 1,041 35:39 [1915 186 25-44
erato . 1917 1,077 95:90 | 1915 149 96-10
We have sketched a map to show the range of dis-
tribution of the variable melpomene with erato in relation
to other races of the two species which are more or less
constant to the south-east and to the north-west. Thus
at Para melpomene is present as thelxiope, while erato occurs
as amazona, and these two forms are more or less constant.
The erato amazona is very fixed, while the melpomene
thelxiope varies only in the amount of yellow spotting, but
not to any extent. Only rarely are such forms as aglaope
to be met with. In British Guiana to the north-west the
other extreme is met with. Melpomene occurs typically
and scarcely varies at all, and incidentally is rather rare,
while erato is represented by the form magnifica, is also
very constant, but is very abundant.
Further to the north-west in Trinidad the two species
are also constant. Melpomene is slightly changed to
euryades, while erato becomes hydara and is constant.
oth species are common, but erato is a good deal the
commoner. The interesting places to get material from
now would be east of the Berbice River in British Guiana
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a large Heliconine collection made in French Gavana. 353
and west of the Saramacca River in Dutch Guiana. Also
the almost totally unexplored country entomologically
between the Oyapock River on the eastern boundary of
French Guiana and the mouth of the Amazon.
It will be seen on reference to the sketch map that the
mountain range that borders the interior boundary of the
Guianas descends on the boundary of Dutch Guiana to
500 ft., while to the east and west it rises to the neighbour-
hood of 3,000 ft. It is thus understandable how the
variable Heliconine forms can extend across Brazilian
Guiana to the north bank of the Amazon at Obydos. It
is still to be discovered why the variable melpomene and
erato should not be found in British Guiana, especially in
the region of the Berbice River or the Corentyn River, as
there do not seem to be any physical barriers. The
climate one would suppose also to be substantially the
same. There may be differences in the seasons. In
British Guiana there are two wet and two dry seasons
over a large area. We cannot get information about
French or Dutch Guiana in this respect, but at Para
there is one long wet and one dry season. From the
general climatic standpoint there is great uniformity, heat
and moisture prevailing with great uniformity throughout
the year, and even if no rain falls for two months the air
is always heavy with moisture, and very heavy dews are
deposited at night.
Marcu 29, 1919.
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New species of Shep lena from ee Part II. el MALcoLmm
CamERON, M.B., R.N., F.E 231
Notes on Australian Sawflies, erat the se Moraes Types” ait ae
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THE
PROCEEDINGS
ENTOMOLOGICAL SOCIETY
LONDON
FoOR--LaE- <VEAR “EOS;
Wednesday; February 6th, 1918.
Dr. C. J. Ganan, M.A., D.Sc., President, in the Chair.
Nomination of Vice-Presidents.
The PRESIDENT nominated Dr. H. Etrrincuam, Mr. A. H.
Jones and Mr. 8. A. NeAve as Vice-Presidents for the ensuing
year.
Election of Fellows.
Dr. Joun Adams Comstock, Curator of the South-Western
Museum, 1275 Bellevue Avenue, Los Angeles, California,
U.S.A., and Mr. James W. Monro, Lieut. R.A.M.C., 2nd
Sanitary Coy., Duke of York’s Head Quarters, Chelsea, 5. W.,
were elected Fellows of the Society.
Exhibitions.
A BEETLE NEW TO BRITAIN, AND ANOTHER HITHERTO VERY
RARE.—Mr. DonistTHorPE exhibited a.¢ and 2 of Caenocara
subglobosa, Muls., a beetle new to Britain which he had bred
PROC. ENT, SOC. LOND., 1. 1918. A
(ats)
from a “ puff-ball”” (Lycoperdon gemmatum) taken at Barton
Mills, Suffolk, on September 9, 1917, together with a specimen
(2) of Caenocara bovistae, Hoff., swept at Battle, Sussex, on
August 2, 1902, the only species of this genus known to occur
in Britain heretofore.
Also specimens of Cryptophagus lovendali, Ganglb., which
he had found in large numbers in a nest of Vespa germanica
in a tree in Richmond Park on November 20, 1917; a species
of which only two specimens had been taken in Britain before,
by Mr. Champion in July 1907, in a hollow in an old beech
tree in the New Forest. Mr. Donisthorpe made some remarks
on the habits, distribution, etec., of these exhibits.
Hemiererous Ova.—Mr. HE. A. BuTier exhibited ova of
the following species of Hemiptera :—
Two species of Pentatomidae, Piezodorus lituratus, Fabr.,
and Pentatoma rufipes, L.; emergence from these is effected
by lifting a lid from the anterior end of the egg; according
to Fabre the embryo is aided in doing this by an apparatus
consisting of a thin membrane strengthened by a triradiate
chitinous framework, which could be seen in the group from
Pentatoma. Chorosoma schillingi, Schml., a Coreid bug, emerg-
ence from which is effected also by lifting a lid, but without
the accessory apparatus. Two species of Berylus, in which the
ovum is elongate and longitudinally suleate, and emergence is
effected by the longitudinal fission of the egg at the anterior
end. Three Reduviidae, Coranus subapterus, L., Nabis major,
Costa, and Nabis rugosus, L. The two species of Nabis have
the shape of a short test-tube bent at the open end and with
the mouth placed obliquely. A Capsid bug, Miris laevigatus,
to which were added the five cast skins representing the five
larval instars of the individual produced from the single
ovum exhibited; and lastly, the ova of three water bugs,
Naucoris cimicoides, l., Notonecta glauca, L., and Nepa
cinerea, Li.
Two SPECIES OF CATAGRAMMA, AND A NEW DYNAMINE.—
Mr. Kaye exhibited from Mr. Joicey’s collection series of the
two Catagramma species pastazza and excelsior with races and
forms of each pointing out that the two groups of insects
were at once separable by the different tips to the antennae.
Cin)
Pastazza and its forms speciosa and excelsa having a wholly
black club, while excelsior and its forms ockendeni, elatior
michaeli and excelsissima have the apical half of the club
ochre yellow. This point of difference did not seem to have
been detected by Staudinger, who first described pastazza as
a form of excelsior, as he differentiated his pastazza by wing
colouring. The excelsior of Hewitson, figured ff. 49, 50,
Cat. vii, appears to be, if not unique, excessively rare. As it
is close to excelsior elatior it might be found in the same
localities in Ecuador, notwithstanding the locality given,
“Amazon.”’ Other races of excelsior are also rare—michaeli
from the Solimoes River and excelsissima from the Madeira
as well as elatior from Keuador are all scarce, ockendent alone
having been secured in some numbers in the Chanchamayo
district of Peru. In tabulated form the two species work out
thus :—
Catagramma pastazza pastazza, Stgr., with ab. speciosa.
S.E. Peru.
Catagramma pastazza excelsa, R6b. (nee Ster.).
Keuador.
Catagramma excelsior ockendent, Obth.
Sele Peru,
Catagramma excelsior elatior, Obth.
Kcuador.
Catagramma excelsior excelsior, Hew.
* Amazon.”
Calagrammea excelsior michaeli, Ster.
Solimoes River.
Catagramma excelsior excelsissima, Stgr.
Madeira River.
A striking new species of Dynamine from Bolivia was
also exhibited, D. agatha, recently figured by Oberthiir,
Lép. Comp., xii, pl. edvi, fig. 3493, but undescribed.* The
* Fore-wing deep velvety black with the base a brilliant blue and a
broad outer marginal band of the same colour broadest on the costa,
where it forms a sort of nail-head shape and tapering rapidly from
ae)
species was wrongly identified by Staudinger in “ Iris,” vu,
p. 225, where he refers to the most splendid of the Dynamine
Species perpetua, going on to describe a black insect with
steel-blue bands on the fore-wing and on the hind-wing.
Perpetua, described by Bates in the ** Journal of Entomology ”
(1865), p. 326, is a green species and has nothing to do with
the present insect.
He further exhibited from his own collection an association
of Heliconine forms from Para, all taken in the months
July and August 1917. There were seventeen H. melpomene
thelxiope, mostly fairly typical, nine H. erato amazona and
three Huerdes tales pythagoras. Although Heliconius melpomene
thelxiope here appeared to act as the model it was not really
so, as H. erato amazona was certainly the commoner butterfly
of the two at Para, while the Hueides always was third in point
of numbers, and in any case reinforced the amazona owing
to the manner of the streaking. It was probably true that
H. erato amazona appeared a little earlier than H. thelaiope,
and thus advertised the colour scheme a little in advance,
so that it was possible that at the end of the time of appear-
ance thelxiope might sustain few attacks, although be present
in some numbers. It was obvious from the specimens that
amazona had been out some time, as all the specimens appeared
orange and not rosy red as in fresh specimens.
A second small association was a well-known one in point
of species, but little or perhaps unknown as to locality. The
species were H. melpomene nanna and H. erato phyllis and
the locality Pernambuco. There were four specimens of the
former and two only of the latter; here again the seeming
vein 3 to inner. Hind-wing deep velvety black with a large oval patch
lying along outer margin between vein 4 and tornus.
Underside of fore-wing blackish with the greater part of the cell
ochreous except for two black marks edged above with blue. Three
white spots forming an oblique apical band, a white spot within the
cell and a dirty white spot near tornus. A double blue subterminal
as far as vein 38. Underside of hind-wing dirty whitish with three
nearly parallel oblique brown bands, the two outer ones united above
the cell by an interrupted blue band. ‘Two eye spots, the upper, the
larger, surrounded with an ochre yellow ring and placed on a purplish
patch. A regular ochre narrow submarginal band narrowly edged
with blue. The underside is very similar to Dynamine onias, underside
white, the upperside strongly suggests unica flora.
Gx)
model being wanna, while in reality it was phyllis, for by the
condition of the specimens it was probable that phyllis was
going over, and it was well known that H. erato phyllis was
always abundant wherever it occurred. Nanna, reaching so
far north as Pernambuco, was of special interest, and from
the four specimens fairly constant, only one showing a hori-
zontal red streak below the yellow transverse hind-wing.
band.
PsEUDACRAEAS IN Mrimetic Assocration.—Lord Rorus-
CHILD exhibited a series of Pseudacraeas in illustration of a
paper on the mimetic associations of these butterflies which
would shortly appear.
A NEW FORM OF PSEUDACRAEA POGGEI, DEW., MIMICKING
THE DORIPPUS, KLUG, FORM OF DANAIDA CHRyYSIPPUS, L., IN
EX-GERMAN Hast Arrica.—Prof. Poutron said that he had
recently received four letters and three consignments from
Capt. G. D. H. Carpenter, who had written from Lulaneuru
on the Central Railway, 17 miles W. of Tabora, at a height
of 3766 ft. From these letters he had arranged the following
communications, of which each section bore the date of the
letter to which it belonged.
Nov. 5, 1917.—*‘ I have had a piece of stupendous luck and
hasten to tell you. A few days ago, on the small kopje of
granite behind the camp, about 300 ft. high, I caught what
I took to be, at first, a couple of Hypolimnas misippus, L.,
the @ variety [vnaria, Cram.] without apical black and white
markings. When I had caught them I thought they looked
a little odd, but as I have not caught a large number of
misippus and have not handled it much, and it’s some time
since I caught one, I thought I must have forgotten the
details of its appearance, and put the specimens away for a
time. (Can you guess what’s coming?) Next day I caught
a female of the type and felt quite sure then that I had got
Pseudacraea pogget, Dew., and it was soon certain when I
caught a genuine misippus form imaria and then a male
pogget. I am now sending you, by registered post, in a
chocolate box by themselves these most exciting specimens—
three of the type and two of the variety, together with the
inarvda.
Cv}
“T have caught lots more. Yesterday (Nov. 4) I got four
more of type and two of the variety, and these will soon be
sent in a large biscuit tin, which is almost ready. This morning
J caught 10 more of the type.” ;
Nov. 14.—‘ Since then I have been catching some daily
and must have got at least 50 specimens with a dozen of
the variety, all in prime condition. It seems remarkably
uniform—I have caught no intermediates between type and
variety.”
Nov. 5.—‘ Is it not splendid for me, for I have always
longed to meet this most splendid mimic, firstly because it is
of the chrysippus association and such a beautiful mimic,
secondly because it is one of my pet genus! But I had
never expected to get it, since I understood it has always
been looked at as a S. African form—though I don’t know
how far north it is known to extend. Still, Lulanguru must
be some hundreds of miles further north of its previously
known area. What excites me most, however, is the uni-
colorous variety, for I cannot remember that it has been
described. If it is really new I shall burst! Put me out of
my anxiety as soon as you can!”
Nov. 14.—* I have only seen them on the top of the kopje
and have never seen a chrysippus there! [A Q of type was
taken Dec. 31.] With pogget is an occasional misippus (I have
caught two and seen a third), and the differences are interest-
ing. Misippus looks larger, its flight is much more floating
and soaring: it is very much more wary and hard to catch;
it sometimes settles on the underside of a twig, as if to con-
ceal itself—indeed, I find it hard to believe, as I think you
believe, that it is Syn- and not Pseud-aposematic.”
Nov. 5 and 14.—*‘ Poggei, on the other hand, in the first
place has a richer quality in its colouring which sometimes
looks more reddish than brown in a fresh specimen; its
flight is heavier and not floating, being more like that of
chrysippus; it is much bolder and less wary than misippus,
and if struck at will nearly always return on its tracks, so that
one can be certain of catching it, as it often comes back right
up to the net to investigate it. It often settles openly on
the tops of low twigs or a branch or on the ground, and waves
(Corvin Ls)
its wings slowly up and down. In fact it almost behaves
like a true aposematic species. Chrysippus itself is quite as
easily alarmed, and indeed I think more so! I certainly
agree with a statement I remember to have seen some-
where that pogget is the best of all mimics of chrysippus. It
is easier to catch than any other Pseudacraea I have caught
hobleyi, Neave, lucretia, Cr., kuenowt hypoxantha, Jord., or
semire, Cr.”
Nov. 5.—* There is a Rhodesian here and he says the style
of country is exactly like parts of N. Rhodesia—granite
kopjes rising out of flat plain, with no actual forest, but
small trees fairly close together. The butterfly haunts two
foci of circumscribed area on the very top of the kopje. They
are nearly all beautifully fresh specimens, whose colouring
has a very rich appearance, and in some lights has a more
reddish tint than either chrysippus or misippus.
“Tam more excited over this find than I have been
over any butterfly matter since I reared Pseudacraea terra,
Neave, or my planemoides, Trim., family of P. dardanus,
Brown. I wish-it did not take so long to hear from
you!”
Nov. 27.—** Pogget goes merrily on—I continue to catch
them, but only the best specimens—and get the variety quite
often. It seems remarkably fixed and definite—I have only
once taken one that shows any intermediary stage—as you
nay see in the model where the white bar is not quite brown,
and there is a httle more black at the apex than there
should be.”
Dec. 7.-** P. pogget is one of the commonest butterflies
on the kopje! It is by far the best mimic of chrysippus.
Not only in close similarity of pattern but in flight is this se—
and it is remarkably un-shy! I have had one settle on my
helmet—-and they frequently come so close to investigate the
net that they almost fly into it, and have even settled on it!
The flight is slower and more flapping than that of any other
Pseudacraea, and has very little of the soaring quality shown
by lueretia, boisduvalii, Doubl., or the forms of eurytus, I.
It will always return to the same spot, flying backwards and
forwards, and sometimes settling quite near to, or even on,
() avail >)
the ground. It is noteworthy how misippus differs. It is
excessively wary, goes off like a shot if struck at, never
settles on the ground, but often on the underside of a spray
quite high up, when it waves its wings, a habit to which
pogge. is very little addicted. I have watched with some
interest to see whether 3 misippus would be deceived by
poggei—but have seen nothing that would lead one to suppose
he was; but I have seen at Kakindu, most unmistakably,
a 3 P. dardanus deceived by Amauris mavius, L., which he
mistook for his own mimetic 92, suddenly arresting himself
in headlong flight to dally a while with the attractive-looking
stranger before finding out his mistake ! ”
Prof. Poulton said that Fellows could well imagine how
interested Roland Trimen, their ex-President and dear friend
of so many of them, would have been at this discovery. He
had often spoken with enthusiasm of the wonderful mimetic
resemblance of the type form of poggei, now completed by
‘apt. Carpenter, to whom Prof. Poulton was sure they would
wish to offer their congratulations.
Four examples of the new form were-exhibited to the
meeting, together with eighteen of the type, including a male
captured in the same locality on July 27, 1917, and sent in a
previous consignment. This latter specimen, although evi-
dently fresh, had been seriously injured, probably by a bird
or lizard, nearly the whole of the left hind-wing having been
torn away.
[Concerning this specimen Capt. Carpenter wrote Jan. 25,
1918: “I hope you will publish the fact that I was com-
pletely deceived by the first P. pogget I caught. I expect I
thought it was misippus, and not having my attention par-
ticularly directed to it put it away without studying it! It
is, however, just possible that I noticed its damaged hind-
wing, and thought I would send a specimen of damaged
chrysippus, and did not study it carefully. Whatever the
expianation I am delighted to think I’ve been had again !
(For the first P. dardanus form planemoides I sent home from
Jinja [captured Aug. 1-15, 1910] and said nothing about it—
did not even remember catching it until you pointed it out
to me in 1913 when I got home.)”]
Cae)
Exclusive of this specimen, Capt. Carpenter’s captures were
as follows :
Pseudacraca poggei, Dew.
1917. | ‘Type form. eter
Oct. 29 -- 2
Noy. 3 3 --
BAe ie: 4 2
eae 10 — |
| reo | 8 |
| 3 2
| =|
aes a, | 2 ee
ined, 5 2
ot 0 3 1
soe eli 2 —
ome 4 — |
ie. 5 etme
Totalsten| sy?) 49sp0 a iy 12
The whole of these were males except two of the type
form, captured Novy. 3 and 5 respectively. Thus the propor-
tion of dorippus-like var. to chrystppus-like type was almost
exactly one to four.
[Since the above was written Capt. Carpenter continued to
make captures up to Jan. 2, 1918, just before his stay at
Lulanguru came to an end. His total captures were 108
males and 3 females of the type form, 31 males of carpenteri—
a proportion of 1 to 34. The third female was taken in cop.,
and carrying the male, on Dec. 6. The female of Nov. 3
shows the most considerable, although very minute, approach
towards carpenteri of all the 111 examples of the type, as shown
in the degree of development of orange along the costa and in
two small internervular spear-head-like patches in the angles
C2")
of areas 7 and 8. These patches are distinct on both surfaces,
but especially on the under. In addition to the specimen
taken on July 27, a male of the type form taken Dec. 15
exhibits extensive injuries evidently inflicted by enemies, the
anal quarter of both hind-wings being torn away symmetric-
ally. Furthermore, 22 males of the type form and 7 of
carpenter? exhibit smaller injuries, of which the great majority
were inflicted at the anal angle of the hind-wing, and, from
their form, almost certainly by birds. Two female H. misippus
accompanied the Pseudacraeas—one of the daria form
“caught at the same time and place as pogge:””’ on Nov. 3,
and one misippus with slight development of white on the
hind-wing, taken Nov. 11.]
Capt. Carpenter had not as yet recorded the proportion of
dorippus to chrysippus at Lulanguru and adjacent localities,
but further to the east and north it was known that dorippus
largely predominated. Thus Capt. W. A. Lamborn had written
on June 3, 1916:—
“T have been much struck by the abundance of dorippus,
the type form being almost absent. Jnaria also seems to be
more numerous than the type, and encedon is almost invariably
a brown form [daira] without any subapical bar at all.”
Out of 40 D. chrysippus collected by Capt. Lamborn in north
central ex-German East Africa, to be recorded with precise
localities by Dr. Eltringham in our Transactions for 1917,
33 were dorippus, 3 albinus, Lanz. (a more or less white-hind-
winged dorippus), 3 chrysippus, and 1 with less white on the
hind-wing than ale/ppoides, Moore. Out of 21 Acraea encedon,
L., 16 were daira, Godm. and Salv., 3 encedon (one approach-
ing infuscata, Staud.), and 2 lycia, F.
Capt. Carpenter's captures were made on what was prob-
ably the border of the area in which the above proportions
obtained, and it was likely that if the Pseudacraea had pene-
trated still further into this area the proportion of the new
form would be found to be much higher to the north and
east.
Mr. 8. A. Neave, who had had an extensive experience of
the type form of P. poggei some three or four hundred miles
south and a little to the west of Lulanguru, wrote to Prof.
( xi )
Poulton from Kambove in the 8.E. of the Congo State,
Nov. 14, 1907: “I still think P. pogget the best mimic of
Danaida (Limnas) chrysippus, even better than misippus—its
flight is so extraordinarily like that of the model. It is rather,
I think, a significant fact that of all the Pseuwdacraeas | have
met with (5 spp.) pogge is by far the most abundant; while
it is bold, and not afraid to expose itself on the wing” (Proc.
Kint. Soc., 1908, p. xv).
Mr. Neave had written on Jan. 15, 1918: ‘‘ That is most
exciting about a new form of P. pogget, mimicking dorippus.
It is suggestive that, from the description of the locality, it
must be decidedly more lightly wooded and therefore pre-
sumably drier, than those in which the type form occurs in
N.E.R. and Katanga. The haunting of * circumscribed areas
on the top of a kopje’ is of course a habit of many butterflies,
but the only Psewdacraea I have seen do it is P. boisduvali.”’
A little later Mr. Neave wrote, after seeing Capt. Carpenter’s
letter: ‘‘ I return herewith Carpenter’s letter, which I have
read with the greatest interest. I myself took poggei chiefly
at medium elevations, viz. from about 2500-3500 ft., but it
occurred up to 4500 ft. on the high plateau 8. of Tanganyika.
It was most numerous in the valleys of the larger rivers,
such as the Lualaba and Luapula in Katanga and the Kalu-
ngwisi and Chambezi in N.K. Rhodesia. It is on the wing all
the year, but is most abundant toward the end of the wet
season, at which time it is to be found in woodland country
among comparatively small trees, much as Carpenter describes.
At the height of the dry season, I only found it in patches of
denser forest with larger timber.* I have not observed any
special association of this species with the tops of small hills
and kopjes, but there is little of this type of country within
the area it frequents in Rhodesia and Katanga.
* With regard to its flight and appearance on the wing |
fully endorse Carpenter’s statements. At very close quarters
one would be perhaps inclined to mistake it for a female of
H. misippus, but at a little distance, especially when on the
wing, | myself found it almost impossible to distinguish
* The habits were also recorded by Mr. Neave, together with the
exact resemblance to the model, in Proc. Zool. Soc,, 1910, p. 35.
(oexiinny
from chrysippus except in the case of very fresh specimens,
which are a trifle brighter in colour. This superiority of
resemblance over misippus or the other mimics of chrysippus
is, I think, mainly due to the flight being so much more like
that of the model. Though hardly so regardless, or rather
unconscious, of danger as L. chrysippus appears to be, it is
remarkably bold on the wing and decidedly easier to catch
than misippus.
‘““The resemblance on the wing between P. poggei and its
model is so close that it suffices to deceive the insects them-
selves, and on at least one occasion I have seen one of each
species chasing the other, and flirting together for several
seconds before discovering their mistake.
‘“Carpenter’s discovery of a form resembling the dorippus
var. is of the utmost interest, more especially as his descrip-
tion of the locality indicates a decidedly drier region than
those I found the insect in, and therefore one in which this
variety of the model may well be the dominant one.”
Pseudacraea poggei, Dew., forma numetica n. carpentert.—
The differences between carpenter and the type form are
almost confined to the fore-wing, just as those between
dorippus and chrysippus. In. the following description the
fore-wing is always to be understood when the hind-wing is
not specially mentioned. The essential difference between
carpenteri and the type form is a reduction in the black fore-
wing markings and the replacement of the white by a paler
tint of the orange ground-colour, changes which transform
the butterfly from a mimic of chrysippus into a mimic of
dorippus.
The reduction of black.—This reduction is chiefly manifest
in the apical region of both surfaces and is remarkably com-
plete, leaving no trace of an edging to the vestigial oblique
bar such as is often seen in other mimics of the same model,
and especially strongly in the inaria 2 of Hypolimnas misippus.
The black apical area persists as a marginal band nearly
uniform with that round the hind-wing and other parts of
the fore-wing—as in dorippus. Within this apical margin
scattered black scales only exist in sufficient numbers to pro-
duce a distinct effect in relatively few specimens, and these
( xiii)
are not the individuals which retain the clearest traces of the
white bar and white spots.
Reduction of black also occurs at the end of the cell,
although the retention of this marking of the type would
perhaps have promoted the resemblance to dorippus—a
resemblance certainly attained in the inaria Q of misippus
by the persistence of a part of the black markings of the type,
as is well shown in figs. 5 and 4 on Plate XIV of Trans. Ent.
Soc. for 1905. At the same time, as is also shown on fig. 3
of the above plate, the black mark placed at the end of the
short cell of poggei is of a very different form from that
which partially surrounds the end of the longer cell of
dorippus. The resemblance in inaria is mainly attained by
the retention of part of the black area altogether beyond the
end of its cell, but in a position corresponding with the end
of that of dorippus.
A third black marking reduced in the carpentert form is
the short internervular black streak near the base of area 1b
(shown faintly in fig. 3 of the above-mentioned plate, but
more distinctly in fig. 3a, representing the under surface).
This streak, occasionally vestigial on the upper surface of
pogget, appears to be always absent or vestigial on this surface
of carpentert.
In both it remains distinct on the under surface, and when
well developed above it is still larger and usually of a deeper
black below. In a relatively few of the type form there is a
small black spot between the median and the junction of the
outermost quarter with the rest of the streak. Below this
spot also is more distinct and sometimes fuses with the streak.
The strongly marked blackened veins of the upper surface
of poggei and its variety may be secondarily mimetic of the °
H. misippus and its form inaria. In both mimetic species
they are far more prominent than in the models.
The black spots on the under surface of the hind-wing of
both pogger and the form carpentert are very variable in
shape and often asymmetrical. The two small additional
spots in areas 4 and 5 observed in a single one out of seventeen
specimens from the sources of the Congo and represented in
Trans. Ent. Soc., 1905, Pl. XIV, fig. 3a, were found in one
(xi 4)
Lulanguru pogget out of twenty-nine examined, and, of a
much smaller size, in one carpenteri, and still smaller and in
area 5 of the right side only in another, out of eight examined.
In a few specimens of both forms the lower discocellular is
blackened on one or both sides, representing a vestige of the
lower of these two additional spots.
The occasional appearance of these minute spots and an
additional one in the hind-wing cell, as well as the variable
condition of the basal streak in area 1b are of much interest,
for they represent features strongly marked in Pseudacraea
clarkii, Butl. In this latter species the spots appear on the
upper surface, although more strongly developed, as also the
streak, on the under (Trans. Ent. Soc., 1892, Pl. X, figs. 1, 1a).
The evanescence of the oblique white bar and white spots.—
The transformation is effected by the scales becoming in part
of a pale orange colour and in part of a darker orange, like
the ground-colour of the fore-wing. In some individuals a
relatively few, and in one (out of eight carefully examined)
a high proportion, of the white scales are retained—a _ per-
sistence especially marked in the pair of submarginal spots
in areas 2 and 8. The pair of spots or only one of the pair
in area 1b are quite as often present in carpentert as in the
type, and these also, although very small, tend to retain the
white scales. In both type and variety this pair is often
present or better developed on the under surface when absent
from the upper or feebly developed on it. It is probable
that the whiteness of these pairs of spots, especially those in
areas 2 and 3, is mimetic of the marginal pattern of dorippus
which is strongly developed in the same areas, especially in 3.
Although always obvious on examination by its paleness
as compared with the ground-colour, the oblique bar would
be invisible in flight or at a little distance during rest. Its
edges, especially the inner, are dyslegnic, contrasting sharply
with the eulegnic bar of pogge. ‘The costal extremity of the
latter bar is formed by a fine white streak, of which traces
are often retained by carpenteri, suggesting at first sight
mimicry of the costal spots of dorippus, but it is unlikely
that so fine a streak would be visible. In cnaria, however,
the retention of the costal extremity of the same feature,
( xv )
and of a pale costal spot on its basal side, appears to be
clearly mimetic.
On the under surface of the fore-wing the mimicry of
carpentert is far closer than that of the type, because of the
differences in the apical section. Here the black area of the
type is overlaid by streaks of white scales, producing a very
imperfect resemblance to the characteristic pale tint of chry-
sippus in the same region of the under surface. In carpentera
the white covering scales are retained, and these, combined
with the orange scales which have replaced the black (as well
as the white over the site of the bar), produce a resemblance
to the corresponding part of dorippus which is far closer than
that between pogget and chrysippus.
The last point concerns the ground-colour of both fore- and
hind-wings, and its resemblance to that of the models. In
Ethiopian examples of chrysippus the upper surface of the
fore-wing is generally of a darker Sienna brown than the
hind, and increases in depth of shade towards the costa.
The fore- and hind-wings of dorippus are more nearly of the
same tint and much paler than the usual tint of Ethiopian
examples of chrysippus, being of a brownish orange and
sometimes of a pale, sand-like colour, and the costal darken-
ing is less marked or wanting altogether. In carpenteri also
the fore-wing is paler than in the type and less darkened
towards the costa, producing a more uniform appearance
clearly mimetic of dorippus.
It is of special interest that, as Capt. Carpenter has re-
marked, the dimorphism between the two forms of Ps. pogget
should be so complete—ftar more so than in the females of
H. misippus or the daira and type forms of Acraea encedon.
The only mimic of chrystppus which approaches pogget in this
respect is Mimacraea marshalli, Trim., with its dorippus-like
race dohertyi, Rothsch., but this latter has not yet been found
in the same locality as marshalli, so that true dimorphism has
yet to be proved for the species.
Among the fifty examples of the type form from Lulanguru,
a single one, a female captured Nov. 3, exhibits a sheht but
distinct trace of orange scaling on the black apical area
beyond the white bar of the fore-wing upper surface (see p. 1x).
(~ xvie *)
[The above description, although originally drawn up from
the specimens captured up to Noy. 13, is applicable to the
entire series, now carefully examined. Specimens with traces
of the extra black spots on the hind-wing under surface were
as numerous in the later captures as in the earlier. <A few of
the later carpenter showed interesting vestiges of the type
pattern towards the apex of the fore-wing.]
A comparison between the details of the mimetic likeness
borne by pogget and the 2 misippus to their model, and
between the patterns of the co-mimics themselves, was pub-
lished by the present writer in Trans. Ent. Soc., 1905, pp. 265-7.
At that time I was not aware of the critical comparison between
the same forms which the late Mr. Roland Trimen, F.R.S.,
had published at a much earlier date, in Proc. Zool. Soce.,
1891, p. 79, based on a single male from Omrora, Angola,
which corresponded in size “with the smaller than usual
D. chrysippus from the same locality.” Mr. Trimen found
that poggei was a closer mimic than the 2 misippus in three
features: “On the upperside of the fore-wings the much
narrower costal black and the absence of the apical white
spot, and on the upperside of the hind-wings the narrower,
less diffuse, inwardly more sharply dentate hind-marginal
black border. On the other hand, the greyish-white clouding
on the underside of the apex of the fore-wings and the con-
spicuous spotting of the abdomen are points which lessen
D. [P.]| pogger’s likeness to D. chrysippus as compared to the
colouring of the corresponding parts in D. misippus. These
two characteristics and the subbasal black spots on the under-
side of the hind-wings are retained generic features of Pseud-
acraea, quite peculiar and unmistakable. ... The rufous-
ochreous ground-colour of the wings exactly accords with that
of Danas chrysippus, and the paler tint of the hind-wings
is most perfectly reproduced; while on the underside the
creamy ochre-yellow ground and the white neuration and black
border of the hind-wings (with also a general resemblance in
the few white-edged black spots) are precisely simulative of
the Danais.”
The distribution of the type form of Pseudacraea poggei.—
The exact distribution of this beautiful mimic becomes a
99
(xvii, 4)
subject of the greatest interest now that Capt. Carpenter has
discovered the appearance of its new form on the borders
of the very region where chrysippus is mainly replaced by
dorippus. The distribution of the type form of pogge7, as
given by Aurivillius in “ Seitz” (vol. xiii, p. 197), is Angola,
Southern Congo and Rhodesia, a summary in every way
confirmed by the following data kindly supplied by Lord
Rothschild, Mr. 8. A. Neave and Mr. J. J. Joicey, as well as
by the material in the Hope Department.
AnGoLa.—At Tring, 13: collected by Dr. Ansorge, Mjene
Indale, 2 (also 3 at Witley); Guimbungo, 2; Samba Acenda, 2;
Mikenge, 1; Makweha, 1; Marimba, 1; Bang Neola, 1; Camba
Caquenje, 2; Katole, Jinga Country, N. Centr. Angola, 1.
At Tring also from the following localities: Loanda, 1
(ex Homeyer Coll., co-type); Ceramba, Bihé, 4 (W. C. Bell);
Bihé, 3 (Edw. Sanders); also 3 at Witley.
Quoted by Roland Trimen in P.Z.S., 1891, p. 79: Omrora,
Ambuella Country, 1 (Erikson); Central Angola (Pogge), 2.
Among the above examples of the type a single one,
from Ceramba, Bihé, is a faithful mimic of a D. chrysippus
with hind-wing pattern intermediate between the type and
alcippus.
S. Conco Strate anp N.E. Ruoprsta.—Mr. 8. A. Neave
has kindly added the following account of the distribution of
P. pogget im the above area, in amplification of his brief note
in Proce. Zool. Soc., 1910, p. 35: “I have been looking up
my notes on Pseudacraea pogget. I should describe it as by
no means uncommon throughout Northern Katanga (in the
southern portion of the Congo State), and the plateau of
N.E. Rhodesia N. of a line somewhere about the S. end of
L. Bangweolo. In my experience it does not occur on the
Zambesi side of the watershed, though I should not be sur-
prised to hear of it being found in Northern Nyasaland. I
have an idea that I have seen or heard of examples from the
Karonga district of Nyasaland, 7.e. the extreme N. of the
protectorate, and one would expect it round the shores of
Tanganyika.”
The following account of the model and co-mimics of
P. pogget was published by Mr. Neave in his memoir ‘* Butter-
PROC. ENT. SOC. LOND., T. 1918. B
( xvii )
flies from Northern Rhodesia and adjacent Territories” in
Proc. Zool. Soc., 1910 :—
Danaida chrysippus, L.—* X common insect everywhere,
but prefers open country and avoids very dense forest. The
specimens are mostly of the type form with occasional indi-
viduals tending to var. alcippus, Cram. I saw one specimen
of the dorippus, Klug, form in the mid-Chambezi Valley in
May, and found it not uncommon a few miles above the
mouth of the Lofu river, near Lake Tanganyika, but did not
meet with it to the south of these localities ” (p. 7).
Acraea encedon, L.—* I took this everywhere. The type
form is perhaps the commonest, though not much more
so than daira, Godm. and Salv. The lycia, Fabr., form
occurs rarely in Katanga and more commonly in the valleys
of the Kalungwisit and Lofu rivers in N.E. Rhodesia ”
(GOmAL)
Mimacraea marshalli, Trim.—‘ I took about twenty indi-
viduals of this fine species in the Lualaba Valley, iv. and v.,
and one other later in the year, x. I also saw a few indi-
viduals in the Chambezi Valley, iv. and v. These Central
African specimens seem to be slightly more heavily marked
than those from Mashonaland. I found its habits and the
nature of its habitat very much as Marshall describes,* but
did not observe it settling head downwards on the trunks as
he records... . I was lucky enough to capture, on more
than one occasion, both this species and Pseudacraea pogget
as well as their model Limnas chrysippus within a few yards
of each other” (p. 42). Mr. Neave’s photograph of- the
insect at rest, reproduced on p. 42, was taken in the Chambezi
Valley.
Hypolimnas misippus, L.—*‘ Occurs everywhere during the
wet season, but is nowhere abundant, especially in Katanga,
though fair numbers of males are sometimes seen. The
typical and inaria forms of female seem to occur in about
equal proportions” (p. 31).
Mr. Neave preserved as a separate series and presented to
the Hope Department the most striking examples of P. pogget
and the above-mentioned model and co-mimies, captured
* Trans. Ent. Soc., 1902, p. 472.
| |
Localities in . | Dates in Bre Acraca : Sie a
S.E. Congo State | 1907 and | SNe cn encedon, £ -seudacraca | M anh: ie
and N.E. Rhodesia. 1908, pase OCHA ioe type form. LON EL» ees
SS 1907 |
a2 | Apr. 18 | — 4(10 others} 1 (1 other 3 (1 other
8 | seen) seen) seen)
ee : ;
Bae [. 19| — = — 2
BING el ee
PA om . 20 = = 2 1
ee :
| ret ies 9° 21 ] 1 — 1 (also | AT.
| as Rohe
Ra retiN (ALL within skoptoles
oo }-mile on
ie Sh i same path.) |
3 | oS ca Apr. 22 1 a 2. 1
4 Gioge=| » 26] 1(7o0r8 | 1 (5 others 1 1 (on edge
= bs perms (AML i : f forest
= “= All in) others seen) seen) of forest,
<q | R500 Tee as other species
iv “a SON of native - 5
ae clearing.) In open)
* oN = :
a Hs Apr. 27| (Numbers | 1 (numbers | 6 =
= | oe | seen) seen) wale
a i: i ware:
DR | S Vici aoe 7 3 1 ae
= | (Native col-
= 2 lectors) |
Pia ies: | : fa =
Zo me Apr. 30 1 = = | 3
e) 3 2 | I a
| 25 May 1 = = 1 =
4 | BA | b. :
MD io} 9 oa —_ « a
— | 3 2s cies or. 3 sed be cs
a : a
5 ca 3 — = 1
Xo ait Sy er
Hi . a8 eee 8 = = = :
B gsa ice :
lay ise! .
OF) genie Se . 9 | 1 (mistaken Be.
Be Sos See for pogge) aE 1
> = Pp « or pc 4
tet tot
pres raed 5: a. = eee
Lualaba River,
NziloGorge: 5 18 - -- 2 =
3000 ft.
4 . June 5 = Pe 1 —
Fall eee, yn)
SF ours ar eran
Cie be alle 5 (very worn a 7
| Salesh eter |
eo or ee ee xe ee ae
7; |
|
| Fe ee S. ove 1908 |
Ch ~
eSaee | Apr. 14 5 = | =
.| 4g gigs =O
<j SY > a S 1 ; : |< 4 = ae x * ha re ae
n| otsnt 50 15 | 1 ae 1
| 2 ae
a | Chambezi |
=| R.,Mpika- May 1) 1 x 1 ae
@ | Kasama Rd.
& Luena distr. |
=| and I. shore J sleet
: une 8 3 (seen re -_
ie) of L. Ba- (seen) 1
ae ngweolo
=) re — - —
| Luwingu, N.
S of L. Bangwe- | Sept. 30 l = 1 _
‘| olo: 4000 ft. |
Totals 26 13 23 | 15
Ce xx
)
( xxe'9
together, and these were exhibited to the meeting. This
series 1s Shown in full on p. xix, in a table to which Mr. Neave
has kindly added notes from his journal as well as the record
of additional specimens.
With reference to the localities Mr. Neave points out that,
in some older maps, the Luapula, after leaving Lake Mweru
(it is generally called the Luvua beyond the lake), is named
“ Webb’s Lualaba,”’ which must not be confused with the
real river of that name—the one we are dealing with—which
is much further west.
In Mr. Neave’s opinion the three dates printed in heavy
type in the Congo list, viz. April 18, 26 and 29, 1907, are the
only ones that give an accurate record of the proportions in
which the insects occurred. At the same time the other less
coniplete data are of value in confirming the conclusion that
the insects are found in the same places, and often at the
same time.
A large proportion of the specimens of all the species in
this table is kept together as a special series in the bionomic
collection of the Hope Department—a series of which Dr.
Eltringham wrote: ‘The general eflect of the group as seen
together is that they are all alike, and when they are arranged
in haphazard manner there is a distinct sense of effort in
counting the respective numbers of the different species. I
know of no instance which could illustrate more forcibly the
reality of the resemblance ” (** African Mimetic Butterflies,”
Oxford, 1910, p. 38).
In addition to the bionomic series many of the other speci-
mens recorded in the table are arranged in the systematic
collections of the Hope Department, together with the follow-
ing examples of P. poggei taken by Mr. Neave in N.E.
Rhodesia : Lower Chambezi Valley, Kasama distr., 3900 ft.,
2; Luwingu, N. of L. Bangweolo, 4200 ft., 1; Luwingu to
mouth of Chambezi R. in L. Bangweolo, 2; high plateau
between L. Tanganyika and the Lofu R., 4200-4500 ft., 3
(one of these exhibits an injury probably caused by an enemy
and noted before capture).
A series of P. poggei, taken by Mr. Neave in the Lualaba
Valley, Katanga, contains the only examples of this species
(Ph ©)
in the British Museum. They include some of the specimens
recorded in the table on p. xix.
In addition to Mr. Neave’s captures the following records
from S.E. Congo and N.E. Rhodesia have reached me :—
At Tring: Riuwe R., Lualaba Valley, near Katanga, S.E.
Congo, 1; Fort Rosebery, about midway between L. Bangweolo
and the Luapula R., N.E.R., 2.
Avr Wittey: N.E. Rhodesia, 5; Chambezi R., N.E.R., 5;
Katonga R., a tributary of the Upper Chambezi R., N.E.R., 1.
Tut Newcastte Museum: Johnstone Falls, Luapula R.,
N.E.R., about midway between Mr. Neave’s Congo and
N.E.R. localities, 2 (formerly in the collection of Dr. H.
Kltringham).
THe Hore Cotiection.—In addition to Mr. Neave’s series a
very interesting collection of pogget, its model and co-mimic
was presented by Sir Horace Byatt (Trans. Ent. Soc., 1905,
p. 263). The proportions of poggei, chrysippus and misippus
in the locality—Kayambi, Awemba Country, N.E.R., near
the Chambezi R., 9° 20’ S., 31° 50’ E., at a height of 3950 {t.—
are shown with singular completeness, inasmuch as the
insects were captured indiscriminately by native schoolboys,
collecting, Oct. 1898-Jan. 1899, for Pére Guillemé. Out of
about 1200 butterflies in the collection the following fell into
the chrysippus-centred combination :—
Dachrysippus, cypetorm xs... a SOOT
re doryppus iGrint, © ew 4 LD
i pogget, TYPeaonmy of ne ae ee fee EG,
(H. misippus, non-mimetic 6 . . . . 36)
by Welpags Ser ee ed eee 7
be Larue S SL Ge eee ee 2
Totaloa see Tetra eae) he A
The proportion of pogger to chrysippus was therefore about
45 per cent (463; the percentage 4°72 is erroneously given in
the paper). Sir Horace Byatt’s remarks on p. 265 are of
much interest in relation to Capt. Carpenter's recent dis-
covery. LP. pogger “is purely a mimic of chrysippus and
shows no approach to dimorphism, ‘This is explicable on the
( xx *)
ground that it is found only where chrysippus is the largely
predominant form, and, so far as is known, it does not occur
in, or has not yet reached, the parts where dorippus is rela-
tively abundant—that is, the desert strip along the E. coast,
extending in the K. African Protectorate inland at least to
the shores of Victoria Nyanza.”’
OTHER LOCALITIES.—Except for Capt. Carpenter’s recent
captures only two other records are known to me: (1) “a
female in the collection of Mr. Hobley which was taken in
German Kast Africa ”’ (Kltringham, “‘ African Mimetic Butter-
flies,” p. 35). It may be conjectured that the specimen
came from near the EK. shore of the Victoria Nyanza, for
Mr. C. W. Hobley’s collection was largely made in the adjacent
Kavirondo-Nandi district (Trimen, Proc. Ent. Soc., 1903,
pp. XXXvili, xxxix). (2) An example, labelled ‘* Uganda,” at
Witley. Its history is, unfortunately, unknown.
THE * FrRuit-FLy ” DRosopHILA AND THE INHERITANCE OF
SMALL VARIATIONS.—Prof. PouLton said that Prof. H. S.
Jennings of Baltimore, U.S.A., who had kindly sent a set of
his papers to the Entomological Society, had remarked in an
accompanying letter, Jan. 16, 1918: ‘* We feel that we have
here in America, in Morgan’s Drosophila, a sort of machine
for grinding out answers to all sorts of questions in genetics,
and now that that question of the inheritance of small varia-
tions has been put to it, it yields an emphatic affirmative
answer.”
Musca AUTUMNALIS, DE G. (corvINA, F.), HIBERNATING IN
A LOFT IN THE IsLE oF Wicut.—Prof. PouLtton exhibited
examples of 66 males and 80 females of Musca autumnalis
captured Dec. 14, 1917, in the cistern-loft of St. Helen’s
Cottage, St. Helens, Isle of Wight. The loft had not been
examined in the winter since Jan. 4, 1915, when far greater
numbers of the flies were present, as described in Proc. Ent.
Soc., 1915, p. xxi. The 146 flies were obtained by sweeping
with the hand into a tin box the individuals of two long
narrow patches on the close boarding of the roof, each stretch-
ing, as in 1915, along the angle made by a rafter with the
roof. By sweeping in this way probably } of the sluggish
flies were secured. In addition to the 146 M. autumnalis
(| xxiii)
a single example of Pollenia rudis, F., was swept into the
box.
The cisterns had been kept quite free from flies by covering
loosely with boards on which layers of newspaper were spread,
A large scattered patch of flies was found between two of the
sheets. It was probable that the loft had been similarly
occupied in the winter of 1916. The repeated choice seemed
rather singular, for the loft was formed within the four steeply
pitched, slated sides of the roof of a small tower, exposed to
the weather and enclosing probably the coldest part of the
roof-space.
HyPo.timnas (EURALIA) DUBIA, BEAUV., FORM WAHLBERGI,
WALLGR., AT REST IN THE SAME SPOT AFTER A WEEK’S
INTERVAL.—Prof. PouLron read an extract from a letter
written by Mr. W. A. Lamborn, Nov. 5, 1917, from Tanga,
Kast Africa. It would be remembered that Mr. Lamborn
had made similar observations on species of Lycaenidae in
S. Nigeria (Proc. Ent. Soc., 1912, p. xxxiii; 1913, p. xxii).
“ T noticed one Sunday a wahlbergi female, with wings injured
in a particular manner, at rest under a mango, and on going
to the same spot a week later I found it still there. This
caused me to hunt for a possible food-plant, andl found two
little nettles of sorts in a fork of the tree. I brought ore
back with the butterfly, but I handled it so clumsily, thinking
at the time of something else, that it escaped, but I feel sure
that this must be the Kast Coast food-plant, and probably
that of HL. usambara, Ward, I expect, so that I feel I made
one little advance on that particular Sunday. I think wsam-
bara the most imposing of them all, and I should so like to
do a little work on it.”
EIPITOLA URANIA, Kirsy, ? = postHumus, F.—Prof. Pout-
TON said that he owed to Mr. J. J. Joicey the opportunity of
exhibiting the type of the West African E£. wrania from the
collection of the late Mr. H. Grose-Smith, and of comparing
it with the series of posthumus in the British Museum. It
seemed a pity that there should be any uncertainty as to the
specific status of one of the most magnificent Lycaenids in
the world, and that Prof. Aurivillius should be obliged to
speak of wrania in the words at the head of this paragraph
(eS esociva |?)
(“ Rhop. Aeth.,” p. 292). Some of the specimens in the British
Museum were undoubtedly conspecific with the type exhibited
to the meeting, but it would be necessary to obtain anatomical
data before deciding that the whole series labelled posthumus
was made up of the variable individuals of but a single
species.
Since the above paragraph was written the question has
been settled. In a considerable series of specimens like that
of the British Museum two groups may be distinguished,
especially recognisable by the differences on the hind-wing
under surface.
Group 1, including the majority of the specimens. The
hind-wing under surface has a golden iridescent ground-
colour, and is traversed by long white nervular and inter-
nervular streaks, the latter like spear-heads in the areas round
the end of the cell. These markings usually extend from
areas 2 to 7 and are sometimes also seen (of linear form) in
la, 1b, and Ie. In some individuals they are yellowish and
in some, probably worn, they cannot be traced.
Group 2. In this, the smaller group, the iridescent ground-
colour is richer and darker in tint, often deep purplish in
certain lights. The white markings are represented only by
the spear-heads and nervular streaks of areas 2, 3, and 4, or
some of them. These reduced pale markings are far more
conspicuous against the dark ground than the more numerous
and fully developed markings of Group 1. The line of the
median in most specimens of Group 2 marks sharply the edge
of a dark streak dividing the hind-wing under surface into
two sections. In the darker specimens this streak is deep
blue in certain lights; in the less dark it is purplish. This
character is especially strongly marked in the males, occasion-
ally evanescent in the females. On the upper surface the
males are also distinguished by a greater development of
black at the apex of the fore-wing and in the hind by a broader
black margin increasing in breadth towards the apex; the
females commonly possess a series of very variable blue spots
extending from the mid costa towards the centre of the outer
margin,
The male type of elion, Doubl, and Hew., from Ashanti, and
(ey)
the female type of belli, Hew., from Cape Coast Castle, belong
to the first of these groups; the male type of wrania, Kirby,
from Cameroons, is a typical example of the second. The
type of Fabricius’ posthumus is unfortunately lost, but the
description is clearly that of a female. Furthermore, Fabricius
refers to “ Jones’ Icones ”’ (5, tab. 77, fig. 2), of which copies
by Donovan and Westwood exist in the Hope Department.
These copies (fig. 2 includes both upper and under surface,
etc.) represent a female of the first group—apparently a
rather worn specimen showing no trace of the white radiate
markings on the hind-wing under surface. Some shght con-
firmation is afforded by the fact that the early West Coast
material was mostly from Sierra Leone, where members of
the first group are common and those of the second rare.
Taking the whole of the evidence together there can be no
doubt that Aurivillius was right in smking both elion and
belli to posthumus.
If, then, the two groups described above represent two
species, urania stands as distinct from posthumus. Consider-
ing the great variability of both groups and the occurrence
together, especially in the southern part of the range, of
individuals from both of them, the differences in pattern are
insufficient to determine the question. I therefore sought the
help of Dr. T. A. Chapman, who kindly consented to examine
the male genitalia of (1) a typical example of the first group
(posthumus) from Old Calabar; (2) a specimen of the second
group, also from Old Calabar, closely resembling the type of
urania; (3) another example of the second group collected
by Mr. 8. A. Neave in the M’panga Forest, Toro, Uganda.
Dr. Chapman reported that (1) was quite distinct from (2)
and (3): “ The Epitolas are very distinct; the most obvious
differences are in the cedoeagus, with a remarkable serrated
projection on the ventral side in posthunius, very straight and
smooth on this aspect in urania; the dorsal projections much
longer in wrania (folded in mounting in both specimens).
The falces also differ very decidedly: the clasps also differ,
etc.”
The differences of pattern here described are recognised in
the arrangement of the British Museum series, but apparently
( xxvi )
no attempt was made to determine the position of wrania,
both groups being arranged under posthumus.
In the British Museum, examples of Group 1 (posthwmus)
are included from Sierra Leone, Cape Coast Castle, Gold
Coast, Ashanti, Kumasi, Accra, Calabar, Old Calabar; examples
of Group 2 (wrania) from Sierra Leone, Old Calabar, Cameroon,
and W. Uganda. In the Hope Department, 4 males from
Oni, 7 miles EK. of Lagos (W. A. Lamborn), and 1 from Old
Calabar are posthumus; 1 male labelled “ trop. Africa” is
Urania.
Both species occur together on the West Coast, but post-
humus predominates to the N. and wrania to the 8. So far
as at present known urania is the only species in W. Uganda,
this locality being represented by one male and three females
collected by Mr. Neave. Of these, the male (M’panga Forest,
Toro) exhibits an increase in the black parts of the upper
surface pattern as compared with W. Coast specimens, while
all three females (Buamba Forest, Semliki Valley) possess the
above-mentioned series of blue spots on the fore-wing upper
surface.
It has not been deemed necessary to repeat the full refer-
ences to the literature given by Aurivillius in “ Rhop, Aeth.,”
p. 291-2.
THE HABITS OF ETHIOPIAN SPECIES OF SARANGESA AND
oTHER HespertpAr.—Prof. Poutron read extracts on the
above subject from a letter written by the Rev. K. St. Aubyn
Rogers from Kongwa, in ex-German Kast Africa, near the
Central Railway and due W. of Zanzibar :—
*¢ Nov. 22, 1917.
“| have been intending to give you my experiences of the
habits of the genus Sarangesa for some time. They are cer-
tainly not exclusively nocturnal, as they fly and visit flowers
quite freely at all hours of the day at all seasons even up to
dusk. I rather fancy the peculiar habit of resting during the
day in dark places is characteristic, perhaps exclusively, of
places with a marked dry season and only in that season.
[ remember at Taveta noticing S. eliminata, Holl., in numbers
down a well shaft, and here I have obseryed a more variegated
Gear)
species, ? S. plistonicus, Plotz (it is not S. motozi, Wallengr.),
in some numbers under the verandah at Kirokwe. This house
has a thatched roof and the verandah is very dark. I have
also seen the dry form of Precis sesamus, Trim., resting there.
At the same time I have found this last species quite freely
at flowers at all times of the day, even the hottest hours.
“ T faney the habit of resting on rocks, and by no means
exclusively dark rocks, is even more universal in Sarangesa
at all seasons. I have little doubt that there are nocturnal
Hesperidae, e. g. Coenides cylinda, Hew., and more particu-
larly Ploetzia cerynuca, Hew., which only appear at the same
time as the Hawk-moths come to light (see my note in Ent.
Mon. Mag., June 1913, p. 130). All the species of Rhopalo-
campta fly at least up till dark, though they are also on the
wing by day. I am inclined to the opinion that all this
group are more truly nocturnal than Sarangesa, though I
should agree that this last has to some extent adopted
nocturnal habits in extended dry seasons.
“Tt looks as if the rains were near, but we have had
nothing more than quite light showers here yet, not enough to
make any difference. I have been up to Kiboriani this week
and saw several much-worn dry-season forms of Precis sesamus,
and P. antilope, Feisth., and one or two P. artaxia, Hew., but
have not seen a single wet form of this genus yet.”
Prof. Poulton said that a similar observation on P. cerymica
had also been made by Capt. G. D. H. Carpenter, who had
captured the insect coming to light at 9 p.m., although there
was evidence that the species was by no means exclusively
nocturnal or even crepuscular (Proc. Ent. Soc. Lond., 1915,
pp. xliv, xlyv).
THE CONSPICUOUS CATOCALINE MOTH HGYBOLIS VAILLAN-
TINA, STOLL, SEIZED AND DROPPED BY A BIRD, AT DURBAN.—
Prof. PouLron said that Mr. C. N. Barker had sent to him
the following observation recorded by Mr. Harold Millar,
who had written, Nov. 27, 1917, from the Zoological Gardens,
Mitchell Park, Durban :—
“T was in scrub bush yesterday, sitting quietly watching
a ‘Noisy Bush-Chat’ [Cossypha bicolor, Sparrm.], when
another of same kind came along, perched itself about 12 in.
( sexvint >)
off the other and started chatting at a great pace; then
there came flying along loosely a common old * peach-moth ’
[Lqybolis vaillantina], which eventually floated towards the
‘Chat,’ which, perched as it was, suddenly seized it, crushed
and killed it, and then quietly let it drop to the ground as
though saying, ‘ What do you mean by disturbing me while
at song?’ I was not more than 10 feet away and could see
all that took place. Quite interesting and instructive.”
In the accompanying letter, dated Nov. 28, from the
Durban Museum, Mr. Barker spoke of the extraordinarily
wet season of 1917. It would be interesting to know whether
the butterflies exhibit any marked effects :—
“The weather still remains persistently wet : one only gets
a few hours’ glimpses of the sun at rare intervals, and this
condition has been continuing since the middle of June,
previous to which we had almost a decade of droughty years.
In all my 41 years’ experience of 8. Africa I have never met
with conditions even approaching those of this year.”
[In a later letter dated Feb. 20, 1918, Mr. Barker writes :
“We have had nearly 80 inches of rain within the last 75
months, and I have been hoping to come across something
abnormal in the melanic line. The black bordering of white
Piermes is extremely developed almost throughout, but I
have met with nothing quite abnormal so far. Insects,
except the hardy common forms, are also unusually scarce,
probably due to the lack of warmth caused by these extra-
ordinary rains. Papilio dardanus, hippocoon and trophonius
2 forms up till just now appear to have been quite as numerous
as cenea. Last Sunday, however, I observed 4 cenea and not
a single example of the other forms. The males are especially
plentiful this season.”’]
[These remarkable rains were also prevalent much further
north, for Mr. C. F. M. Swynnerton wrote, Feb. 2, 1918, from
Chirinda in 8.E. Rhodesia: ‘‘ A wonderful season here. We
have had some very wet ones before, but this beats them all.
We have had rain practically daily since about the 4th of
November : over 45 inches in January, and February threaten-
ing to beat it. The effect of such a season on insect life
should be interesting to note. It must indirectly have been
(sXe)
favourable, as there is bound to have been a great mortality
amongst young birds. ‘Two young owls, full-fledged and fend-
ing for themselves, that frequented my coffee plantation were
both found dead, emaciated and with empty stomachs.
Directly it must have been very unfavourable to butterflies
at any rate: it will be interesting to note the numbers in
which they appear later.’’|
THE SESIAS MIMICS AND NOT MODELS OF THE HYMENOPTERA.
—Prof. Poutton said that he wished to draw attention to an
unfortunate misconception in the recently issued part of
M. Charles Oberthiir’s beautiful work, “‘ Etudes de Lépido-
ptérologie comparée,” Fasc. xiv, 1917. On p. 131 M. Oberthiir
makes the following statement in a passage kindly translated
by Mr. E. A. Elhott :—
All insect hunters have testified (constaté) that the Sesvas
are imitated by a considerable number of insects of various
Orders, especially Hymenoptera and Diptera, but also Ortho-
ptera. These insects, mimicking the external appearance of
the Seszas, live at the same time and in the same places as
they do. When searching at Monterfil for that same Ses/a
uroceriformis. which I have already mentioned several times,
I have been entirely deceived by the flies and even by grass-
hoppers which, when among the clumps of furze, present an
appearance analogous to that of the Lepidoptera. I fancied
first that I saw a Sesia, but was never long before I detected
the deception caused by this mimicry.”
Prof. Poulton said that it was important to correct this
statement as promptly as possible. So far from the view
expressed above being the generally received one, it was the
first time he had heard of it, and it was contradicted by
all the names ending in -formis which were so plentiful in
the group. It was unnecessary to refer to the number of
memoirs in which the Sesias were spoken of as mimics of the
Hymenoptera.
HARPAGOMYIA AND OTHER DIPTERA FED BY CREMASTO-
GASTER ANTS IN 8. NicER1a.—Prof. Povutron said that he
had just received a letter from Mr. C. O. Farquharson, dated
Dec. 15, 1917, from Ibadan, describing this most remarkable
association in an entirely new part of the world. Mr. Donis-
(0 sexe” 3)
thorpe had kindly informed him that, so far as he was aware,
the only published record was that of Edward Jacobson,
who observed Harpagomyia splendens, Meij., fed by the ant
Cremastogaster difformis, Smith, in his garden at Batavia—
Tijd. v. Entom. 52, 158-74 (1909); Notes from the Leyden
Museum, 81, 246 (1909)—and subsequently at Samarang,
Central Java—Tijd. v. Entom. 54, 158-61 (1911), 3 Plates.
Jacobson figured the larva and pupa and reproduced photo-
eraphs of the gnat being fed by the ant.
It was to be hoped that specimens would soon arrive so
that the Nigerian species of Cremastogaster, as well as the
other Diptera which Mr. Farquharson observed being fed by
them, might be studied and if possible determined.
“Many things remain incomplete, but I can honestly tell
you that I have never described what I was not certain that
I actually did see. At times, indeed, I have seen such curious
things that I was afraid to describe them on one observation
in case I were wrong, for I could scarcely credit the evidence
of my own senses. On one occasion, for example, I was
certain that I actually saw a mosquito (at Agege) obtain
regurgitated food from a Cremastogaster. J am sure it was
a Slegomyia.
“Tve just come back from my evening stroll. I went
down to our old haunt (Lamborn’s and mine) to look into the
welfare of two Lycaenid larvae that have, for the last few
days, been slowly devourmg a happy family of Coccidae
(? Lecanium) on a young plant of Imbricaria maxima. Of
them more anon. Having still a little daylight to spare I
went to the old * Hewitsonia tree,’ and there saw at least
half a dozen mosquitoes hovering over the Cremastogaster
‘campus.’ There was light enough clearly to see three of
them at the same game—not Stegomyias and not Anophelines.
I had no tubes to collect them; I was tired when I went out
and didn’t expect to get the length of the old tree, but I
know now that [ll see them again. But I wish I'd been in
time for the mail. I took the Stegomyia at Agege in a tube
which I failed to notice at the time to be moist. When next
[ looked at it I found it dead and sticking to the wall of the
tube. I had a reaction, doubted my eyesight, left the tube
Cao a)
lying about, and saw the mosquito next floating in the alcohol
between those Catochrysops pupae. These I had accidentally
put into the same tube a day or two later, and the observation
must have been made about that time.”
Dec. 19, 1917.—** I had to go to Agege to pay the labour
there; on Friday, Dec. 14, the day before I left for there, I
thought Pd like to go down to the famous Cremastogaster-
Hewitsonia-Argiolaus tree (IL forgot Iridopsis) just to have
another look at the mosquitoes, to make sure that they really
were there. I captured two, easily enough, in little glass
tubes, one with its precise ant and the other not. The precise
ant, finding itself imprisoned and annoyed, attacked the
unfortunate mosquito and killed it. (In a confined space they
will kill the softer Lycaenid larvae.) Hence I had to forego
the precise ant in the case of the other. On the tree I could
make out what looked like white banding on the mosquito,
and went home to look more leisurely at my find. Landed
there, I got a bad attack of what is known as ‘ cold feet.’
I knew little or nothing about mosquitoes, but had vague
recollections of a picture in a wonderful official compilation
known as the * West African Pocket Book,’ that of a Stegomyia,
described in the accompanying letterpress as exhibiting the
pattern of a football jersey. (No wonder the unfortunate animal
is a victim of yellow fever!). But somehow the proboscis
of my myrmecophile didn’t seem to fit into the scheme of
things. Its proboscis wouldn't, anyhow. Jé produced the
local * chill,’ for I couldn’t recall any mosquito like it. I
began to wonder if it could really be a mosquito after all,
but its ‘ poise’ when alive, with its hind legs en lair, and
everything else appeared to be unimpeachable. None the
less I decided that I couldn’t wait till I heard from England,
so I decided to take it down to my friend Mrs. Connal at Yabe
when I went to Agege. This I did. I sent it down a day
ahead of myself with solemn injunctions not to treat the
matter with levity, it being no common mosquito, being in
fact a myrmecophile. When I reached Yabe I found that
there is next to nothing new under the sun! I’m quite sure
now that what Vl get back from Lamborn will be a callous
recommendation to go to his old office library cupboard, find
{ xxx 5)
therein a work of somewhat forbidding exterior described as
‘A Monograph of the Culicidae of the World, by F. V.
Theobald (vol. v), im which, on pp. 547 et seqq., I shall find out
all about it. Mrs. Connal assures me that it is at least a
new Nigerian record. She had never met a Harpagomyia
before—it is H. trichorostris, Theobald—but there can be no
doubt that that is the correct identity of my find. And
there, on p. 548, it is set down without comment, ‘ They are
myrmecophilous insects’! If the British Museum hadn’t
bound that work in such a cover, ('d probably have found it
out for myself. I am ashamed to confess that I had never
even looked inside it. The book, of course, is devoted to
melancholy facts of existence out here, which is one reason
why I didn’t care to look into it, but really publishers ought
to exhibit a little more psychological insight. It really is a
pity that it has not as worthy a cover as, for instance,
* Wheeler on Ants.” I am puzzled about the name Harpa-
gomyia, which I take to be derived from dpzagw, to seize,
and pia, a fly. The name suggests a synechthran rather
than a symphile. From my observations I should class it
as a symphile rather than a synechthran. Wheeler's biblio-
graphy makes no reference to Meijere, but the latter’s de-
seription of the genus would, I imagine, have just about
synchronised with Wheeler’s publication. At the worst it is
a mild €y@pa, in the form of highway robbery without violence,
if not indeed mere alms solicitation by a sturdy beggar.”
Dec. 23, 1917.— I reached the tree just after ten; I had
seen an Jridopsis larva yesterday which I thought I might
safely leave for a day or two, and went along to see that it
was all right. I hope it is, for I regret to say I couldn’t find
it again. I may, however, find the pupa on further search.
I saw quite half a dozen Argiolaus pupae (the * gall’ species).
I saw their larvae coming down a day or two ago. One I
found to be parasitised by a Cordyceps, only the conidial
(Isaria) stage being present. I next examined a half-calabash
of water that I had placed in a hollow of the tree to see
whether any mosquitoes had oviposited—I am in hopes of
inducing Harpagomyia to do so. I failed to get one in the
house. I found a number of ‘ rafts,’ but I don’t think they
(soe |)
are those of Harpagomyia. I am in hopes, too, that I may
get ova of a very large mosquito, I think a Toxorhynchites,
at the same time, for I frequently see them near the tree.
They do not bite man, and I am wondering whether they
have anything to do with ants. I then had a look at some
Lycaenids (Hpitolas, I think) feasting on Coccid secretions on
a shrub hard by the ant tree, the Coccids being Cremastogaster
attended. I noticed a few small Dipterous flies apparently
trying to get a share of the Coccid good things, but just then
decided that they didn’t look very interesting. Hard by the
ant tree are one or two Funtumias (native rubber—A po-
cynaceae), on the stems of which the ants also run about, and
on which I captured on previous evenings some ef the Harpa-
gomyiae, “in flagrante delicto.” I thought P'd have a look at
that too, and to my surprise found quite a number of the
mosquitoes as busy as could be, I think more of them than
I have seen at dusk. I didn’t leave the neighbourhood till
a little after noon, and they were still there. The place is
moderately shady, but by no means ‘forest’ shade. I was
there again at three this afternoon, and they were still busy.
They are unquestionably day fliers [also observed by Jacob-
son|—like Stegomyia, curiously enough. But for the time
they became of secondary interest. For almost the first
thing I saw was a small fly [2 species of Milichia] apparently
‘chivying’ an unwilling ant in a very daring manner. The
ant stopped, apparently in despair of shaking off the impor-
tunate Dipteron. Immediately there occurred the usual
osculation which signifies that one ant is about to offer, or
at any rate part with, a drop of regurgitated food to another,
but in this case to the fly. At first 1 thought the fly might
be predaceous and was about to attack the ant much as a
Bengalia attacks the Driver pupa. When a Harpagomyia
solicits food of the ant it stands directly in front, but this
fly, having induced the ant to stop, or rather in order to
induce it to stop, comes up from the side, and the ant, if
willing to oblige, turns its head half round. The flies—for
I saw quite a number of them at it—frequently, having got
a little at one side, rush round to the other before the ant
has time to move away, and get a little more. They are
PROC, ENT, SOC. LOND., II, Iv. 1918. )
( xxxiv )
astonishingly active and expert at getting out of the way of
ants that come up behind them. They rarely settled outside
the track of the ants. I concluded that one or two that I
saw in that position were, for the time, replete. When I
brought a little glass tube up to them—to within a quarter
of an inch, and not with any great caution either—they flew
an inch or so over the stem of the tree, and if their flight took
them once more amongst the ants, they simply, as it were,
‘watched points,’ taking care not to let an ant get them
from behind, but making no attempt to importune them as
they passed. I saw several, presumably hungry, flies alight
right in the ‘busiest’ part of the track and immediately
begin ‘ chivying’ the ants—that is really as good a descrip-
tive term as I can find. An ant coming up to meet a fly
would dodge to the side. The fly immediately turned round
and ran after it. Their actions were extraordinarily like
those of the importunate beggar. If the ant took no notice,
further than to keep on dodging out of the way, the fly didn’t
waste much time, but turned round and importuned another.
Those that refused to be ‘ bled’ or * touched’ seemed to show
no serious resentment and made no attempt to drive off the
beggar by force. Cremastogasters running up and down a
tree are constantly making little reeurgitory exchanges, a
momentary ‘ osculation,’ and each hurries on its way. If
anything the fly and ant exchange lasted rather longer, but
the ant continued on its usual hurried way just as if it had
met one of its own kind. It is just the same when Harpa-
gomyia is the other party in the transaction. Harpagomyia,
however, hovers an inch or less over the line of ants (at times
resting on the stem and dodging out of the way when neces-
sary), till it sees what is presumably a likely ant. If the
ant is running downwards the mosquito drops down (in
flight) also, keeping a little in front of the ant—as near as
possible without touching it. The ant tries to evade it, but
the mosquito as a rule declines to be put off, and the ant at
last stops. The mosquito quickly settles and the usual rapid
exchange begins, the mosquito thrusting out its proboscis—
which when not in action is carried bent under the body
much like the rostrum of a Reduviid bug—so that the swollen
( xxxv )
end is practically within the ant’s jaws. I have seen the
ant’s palpi (not the antennae) vibrating on it. The swollen
portion of the proboscis is undoubtedly capable of independent
movement. I may say that the mosquito is not * nervous,’
and I have had no difficulty in several cases in standing with
my eyes sufficiently close to the two insects to make out the
ant palpi and the proboscis movement in the mosquito. The
ant raises its head slightly when the exchange takes place.”
Dec. 27, 1917.—** On Xmas Day also I made another quaint
observation. I have been looking about for other Dipterous
myrmecophiles. In my search I came on a large crowd of
Cremastogaster sp. on the trunk of a Saman tree (Hnterolobium
saman)—an introduced shade tree. I thought from the
appearance of them that they were about to start up a new
nest. All were workers, but I think they came from another
large nest not far away. On closer examination I was
astonished to see that there were a large number of dead
ones sticking to the rough bark of the tree in all sorts of
attitudes, but looking as if they had died there and had
not been carried up and afterwards ‘dumped’ by tired
workers. Some were in fact still moribund. I soon noticed
some curious little Diptera [Rhynchopsilopa sp., Ephydridae]
which I thought might be the same as those I had seen on
the Harpagomya hunt. They are, however, quite different.
I soon became interested in their doings, for they settled
among the ants, dodging about when a worker approached
them, but refusing to go far away. I thought I had only
to wait and see more able-bodied beggary. What I saw
was something quite new. I saw it repeatedly, as often as
I liked, and so tame were they that I could actually study
their doings through my pocket lens. When they saw a dead
ant, that had expired in such a position that its abdomen
was easily accessible, they alighted on it. For such small
flies they have a huge proboscis. This they thrust into the
appropriate orifice and fed, not this time on stomadeal food,
but on proctodeal. Pirouetting neatly on the abdomen of
the dead ant, they were themselves—but for the wings, which
when in rest stick up from the body at rather a high angle—
not unlike ants. When in the act of ingesting the abdomen
(. =xxvi)
was raised and lowered gently, and I could also make out the
brilliant white halteres in motion upwards and downwards.
When the abdomen was raised the halteres were depressed
together. I really think their association with ants is not
accidental. I got two or three pairs, and have been trying
to induce the females to oviposit on stale fruit, but without
success. I cannot account for the death of so many ants.
Hundreds of a Pheidole were running about, in many cases
carrying off dead Cremastogasters, with little or no molesta-
tion. Ido not for a moment think the Pheidoles, numerous
though they were, could have caused the slaughter. I am
inclined to think the ants must have come from a ‘ foul’
brood. I have put up a lot in spirit for examination, and am
keeping the nest under observation. They are still in the
same place, and the little flies are still busy in their curious
and rather unpleasant way.”
Dec. 29, 1917.—*‘ I have been laying traps for Harpagomyia
ova in the form of bits of calabash with water placed in the
hollow stem of the ant tree. Dve got hosts of larvae of
different sorts, but four have outstripped all the others—great
red forms with white undersides which are predaceous on the
others. I feel sure they are Toxorhynchites; I think the
other larvae are Stegomyia.”
Mr. DonisTHORPE said it was of the greatest interest that
Mr. Farquharson had observed in 8. Nigeria the same extra-
ordinary phenomena that Mr. Jacobson had first discovered
and described in Java. He stated that the behaviour of the
gnat as described by the two observers, although on the
whole similar, differed slightly in some respects. Jacobson
records that the Dipteron stood in the track of the ants, and
that when an ant ran between its legs it supplicated for food,
and was then fed as described by Farquharson. During the
process the wings of the gnat were so rapidly vibrated that
the nervures of the wings did not appear in photographs
taken of them while feeding. Jacobson had discovered and
figured the larva and pupa of the Harpagomyia. He says,
however, that the eggs, which he does not figure, are laid in
branches of trees which the Cremastogaster had deserted on
account of their having been flooded by rain. The eggs may
(FEp-0.0.4'gi))
also be laid elsewhere, inasmuch as the larvae appeared in
the bowl of water in the glass case (containing the captive
ants) into which he had introduced a number of gnats. The
larvae are easily recognised by their yellowish-white colour and
by their habit of lying on the bottom of the vessel. Jacob-
son records that those nests of Cremastogaster which were
most freely attended by the Harpagomyia consisted almost
entirely of the small type of workers, and he considered that
this was brought about by the amount of food taken from
the ants, and therefore diverted from their larvae. He
furthermore states that he had never found females, but
only males and workers, in such nests. Mr. Donisthorpe said
that this observation was of special interest to himself, as
he had been working for some years on the causes by which
females are produced in ants’ nests. He had, for three years
running, bred winged females from eggs laid in captivity
by a community he had kept in an observation nest for over
seven years, and for the first time last year in another com-
munity he had observed during five years, and he was of
opinion that these positive results had been brought about
by the amount of food with which these two nests had been
supphed. Ants have been kept in captivity by very many
myrmecologists for over 100 years, and in all that time winged
females have only once before been produced from eggs laid
in captivity, viz. when Lord Avebury bred five winged fusca
females in an observation nest in 1880. The last-named
observer also thought that his success might be accounted
for by the fact that this community had been very well fed.
Some authorities also considered that the presence of
pseudogynes in ants’ nests was brought about by the ants
taking too much interest in the beetle Lomechusa and its
larvae, and in consequence neglecting their own brood. It
will be of much importanee if Mr. Farquharson should find
that those nests of Cremastogaster which are most attended
by the Harpagomyia in 8. Nigeria are also unable to produce
females.
Mr. Donisthorpe had also found flies of the genus Melichia
associated with ants in this country, viz. M. ludens, Wahl.,
with A. (D.) fuliginosus at Darenth Wood in 1909, and again
(| xxxvui_)
at Oxshott. It was always so scarce that there was no chance
of watching its habits.
Mr. F. Mure said that he first saw H. splendens at Mr.
Jacobson’s house in Batavia at the time when he was making
observations on them. His published figures and photographs
of them and his description of their habits were very accurate.
Mr. Muir afterwards saw them in the field in Buitenzorg and
Pasoeroean (Kast Java), and in the latter part of 1915 dis-
covered another species (stiJl undescribed) in Taihoku in
N. Formosa. Charles Banks had described similar habits in
a mosquito in the Philippines. *
[Since the meeting of Feb. 6, Prof. Poulton had received
an answer from Mr. Farquharson to some of the questions
suggested by Mr. Donisthorpe :—
Mar. 22, 1918.—‘ You wish to know whether the associated
ant-nests produce winged forms. They do. There’s no doubt
of that whatever. I should say that it is entirely unlikely
that the Harpagomyias would have any effect at all, for their
numbers are relatively very few. I may say that of five
Cremastogaster nests known to me, I mean intimately, that I
visit regularly, all are frequented by the mosquitoes, but one
doesn’t see more than half a dozen at a time. Besides, the
ants. if not omnivorous, are certainly at times carnivorous,
and at other times—regularly almost—frequent the glands of
plants, collecting nectar all day long, in addition to ‘farming’
Coccidae of different kinds. I doubt if even the largest
colonies, which must contain enormous numbers of inhabitants,
ever experience anything like famine conditions or even
moderate scarcity of food. I should think there would always
be enough and to spare. You know how worker ants stop
each other and exchange a little regurgitated food, a momen-
tary transaction almost, both passing quickly on their way.
The mosquitoes do exactly the same. They will drop down-
wards just over an ant that is hastening along in the usual
way. The ant may stop and give an alms to the beggar,
passing on a moment or two later as if it had just met a
friend, and the mosquito flies up and down again till another
obliging ant is met. At times the selected ant simply ignores
the mendicant, but shows no resentment, nor does the mos-
(zoom |)
quito press his or her attentions. (By the way, I haven’t
verified whether the habit is confined to either sex or not.
I must look into that.) I had Dr. and Mrs. Connal here on
a visit not long ago, and was able to demonstrate them at the
top of their form. I also had the pleasure of showing them
at work to Mr. H. N. Thompson (the Chief Conservator of
Forests), a useful array of witnesses for any doubters to tackle,
I was also able to demonstrate the other Diptera.’’}
Wednesday, March 6th, 1918.
Dr. C. J. Gauan, M.A., D.Sc., President, in the Chair.
Election of Fellows.
Col. WitFrRip Wm. Ocitvy Beveripcr, R.A.M.C., C.B.,
D.S.O. (on active service), c/o J. H. Durrant, Esq., Natural
History Museum, §. Kensington, S.W., and Messrs. Patrick
AvuBREY Hucu Smiru, Sconner House, St. German’s, Cornwall,
and 28, Bruton Street, Berkeley Square, W., and LioneL
JuLiAn Watrorp, The Cavalry Club, Piccadilly, W., were
elected Fellows of the Society.
Exhibitions.
MYRMECOPHILE DipTrERA COLLECTED AND THE CULICID
TOXORHYNCHITES BRED BY Mr. C. O. Farquuarson In 8.
Nicerta.— Prof. Poutron exhibited the specimens referred to
in Mr, Farquharson’s notes communicated to the last meeting
of the Society (p. xxix), and received at a later date. The
accompanying letter, written Jan. 26, 1918, contained the
following paragraph: ‘“ ve sent two little sets of the ‘ ant-
flies? and some Harpagomyias, besides the huge Toxorhyn-
chites with a larva of the species. The larva is red dorsally
and white ventrally like a tiny fish. They are predaceous as
larvae on things like Stegomyias and even Psychodid larvae.
As imagos they don’t bite, but are said to be anthophilous.
(atts)
[ve had no luck in getting Harpagomyia bred, except that
the Toxorhynchites oviposited in. my calabashes.”
The specimens exhibited included 2 3 and 2 2 Toxorhyn-
chites brevipalpis, Theo., with their pupa-cases, 3 3 and 3 9
Harpagomyia trichorostris, Theo., one of the males being
specially associated with a % ant—Cremastogaster buchneri,
Forel, near the r. alligatrix, Forel. The two Culicidae had
kindly been compared with the types by Dr. G. A. K. Marshall,
the ant with specimens named by Forel by Mr. A. H. Hamm.
The “ ant-flies,” also exhibited, had been kindly examined by
Capt. J. E. Collin, who found that the “‘ mendicants ”’ were
represented by two distinct species of Muilichia, while the
‘ proctodeal feeder’? was a new species of the genus Rhyn-
chopsilopa, Hendel (Ephydridae). The type species was from
Formosa. It was of much interest that the males and females
of Harpagomyia appear equally to solicit the ants for food.
Jacobson mentioned the males and females occurring together
in Java, but did not record this fact.
THE NIDIFICATION OF OSMIA AURULENTA, PANZ.: A COR-
RECTION.—Prof. Poutron said that he had recently received a
letter from Dr. G. Arnold, in Bulawayo, correcting the state-
ment, on p. xxxili of the Proc. Ent. Soc. for 1916, that he
had bred Osmia aurulenta from whelk shells, on the Wallasey
sand-hills. The shells were a species of Helix, probably
nemoralis.
Capt. W. A. LAMBORN’S JOURNEYS WITH THE Hast AFRICAN
VETERINARY Corps IN 1916.—Prof. Poutton said that he felt
sure that Capt. Lamborn’s letters, written from the localities
at which he took the butterflies mentioned in Dr. H. Eltring-
ham’s paper in our Transactions for last year (p. 322), would
be of interest, not only in relation to the insects but also
because of the brief descriptions of a part of late German
Kast Africa :—
“clo Veterinary Department,
* Nairobi, British Bast Africa,
“12. 4. 16.
“T left Nyasaland in late January and only reached Mom-
basa in the last week of March, having had to wait a con-
siderable time both at Beira and at Chinde for steamers. It
( xii)
has been a most grievous waste of time, for at neither place
was any economic work possible, the country round being
swampy and uncultivated, and being in daily expectation of
a steamer’s arrival I was unable to go farther afield. How-
ever, I took a few butterflies at each place, just the ordinary
common varieties. I have had no letters except three for the
past five months and so am feeling quite out of touch with
every one.
“There is still further delay here in regard to my com-
mencing work. The Army Council wrote out that I am not
to have a Commission and so I joined the forces, the only
civilian among thousands. The position was absolutely un-
tenable, and my experiences unenviable, and I am now in
Nairobi while the Colonel of the Vet. Section, to which I am
to be attached, is endeavouring to adjust matters. The
Govt. Entomologist was given a Commission at the start.
‘The work required appears to be simply to map out fly
areas in German East Africa as the country gradually falls
into our hands. Research work will probably be entirely out
of the question, but I shall do my best to continue along the
lines I followed in Nyasaland.
“The general opinion seems to be that the campaign here
will only last a few more months, and it is said that the native
troops on which the Germans are so much relying are already
disorganised and out of hand.”
*““ New Moshi [37° 24’ E., 3° 24’ S8.],
le OWV lO:
* A wet Sunday morning gives me an opportunity of writing
you a line. I have been attached to the Hast African Veteri-
nary Corps with rank as Captain, and have now made a definite
start on my duties by surveying for tsetse a horse camp in
the vicinity of this place.
“Tam now about to trek away towards the west along the
foot-hills of Kilimanjaro, searching for the flies along the road.
It is by no means pleasant just now because there is a constant
drizzle of rain, and there is an appalling amount of liquid
mud.
“| have made already a small collection of Lepidoptera on
the mountain slopes, but, as you will understand, one cannot
( xlii_ )
put much heart into such work in these anxious and trying
times.
* Acraea encedon is fairly plentiful and I got one large
lycia form, a splendid specimen, which I did not recognise as
such on the wing, and there are various species new to me
but which are doubtless common enough.
“Tt is perhaps early days to express an opinion, but I am
by no means sure that my services are going to be of any real
value to the military authorities. However, I shall of course
see the matter through, hoping to justify my transfer here by
the discovery of the breeding-grounds of the local tsetses,
Glossina pallidipes and longipennis, pupae of which have been
urgently needed for a long time for trypanosome work in the
laboratories.
“Carpenter has just written me his usual cheery form of
letter from the 8.W. corner of Uganda.”
[Ufiom?, 35° 50’ E., 4° 16’ 8.],
3.6: 116:
“Most of my days are spent in steadily trekking along
military paths in search of tsetses, and I have now covered
so much ground that I am no great way behind the sphere of
operations. I have defined several large fly areas, but beyond
that have not been able to do a great amount of entomo-
logical work. However, I try to add a few insects daily to
a collection, and am not forgetting Lepidoptera, Acraeinae in
especial, which seemed to me to be probably of most interest.
“The country as a whole where I have been was arid in
the extreme, lack of water being a serious trouble at times,
but every now and again there has been a good river with
insects fairly numerous in the vicinity.
* T have been much struck by the abundance of dorippus,
the type form being almost absent. Jnaria also seems to be
more numerous than the type, and encedon is almost invariably
a brown form [daira] without any sub-apical bar at all. I
have twice met dardanus 9s. The first settled with outspread
wings on a flower, and I said to myself at once, “What a
huge psyttalea, and until I had it in the net I did not realise
it was a Papilio. It had a white pattern on a black back-
sround just like the Amawris, but unfortunately the specimen
( xl )
will not be forthcoming. I put it alive under my helmet
while considering the feasibility of trying to breed from it,
and in the meantime it escaped. The second female—I
forget the name of the form, but do not think it is quite
trophonius—has light sulphur subapical markings and light
brick-red on the hind [or inner] margin of fore-wing and centre
of hind-wing, with black margin [the new form lamborni
described in Trans. Ent. Soc., 1917, p. 335].
“T trust that when this letter reaches you the news will
have got through to you that the campaign is over.
“Some of the 9 tsetses here have a puncture or cicatrix in
the centre of the abdomen, the causation of which I am
hoping to be able to investigate. It will be almost out of the
question when the war here is over, the country being very
thinly populated indeed, and so inhospitable in the regions
where I have been.
“Tam longing to be able to have a good butterfly talk with
you and to see the recent additions—all by other people this
time—in your department. I have only some ten months to
do to the end of my tour.”
“The Front, German East Africa,
[Ufiomi was the last halt before reaching the Front],
wel ay (0) MUG
‘“ T reached some days ago the scene of actual warfare, and
am now held up indefinitely behind the trenches until such
time as a move takes place. Apart from the excitement
produced by the German shelling—they put fifty-three shells
about two miles behind my tent yesterday mornine—life is
very dull, for the district is so arid that insect life seems
almost non-existent, and I have to try and console myself by
perusing Sharp’s ‘ Insects’ and the last volume of Gibbon.
‘“* Here no one seems to know at all what developments are
likely to take place, though further back the people seem
much better informed.
“ At my last halt I found a well-watered fertile valley in
which were a fair number of Lepidoptera, some of which I was
able to collect. A species of Amauris LA. albimaculata, Butl.]
was quite common—I must have taken at least thirty—and
with it a Kuralia [dubius mima, Trim. |
a most perfect mimic
( -xhv )
—of which I took three. I shall despatch all this material
directly I get back to B.E.A. [Of the above Amawris model
and Hypolimnas (Buralia) mimic, Capt. Lamborn took, in the
wooded river gorge at Ufiomi, on June 4th, 15 models and 1
mimic ; on June 5th, 6 and 0; on June 6th, 3 and 2, respectively. |
“ T hear little news of the outer world, and have no mails,
but hope all is going well elsewhere.”
[Handeni, about 38° E. and 6° 8., on 23. 7. 16},
245706!
“T continue to trek mile after mile defining tsetse areas,
but without, I am afraid, any benefit resulting thereby, and
the only consolation I have is that I am carrying out such
instructions as the military authorities have given, and can
do no more.
‘““T have collected now a considerable number of insects,
including long series of Acraeinae. One or two look really
interesting, but apart from them the butterflies are just the
ordinary things.
“You probably hear more than I do as to the progress of
this campaign. We seem, thanks to the energy of the South
Africans, now to be making good headway, but I am no
longer so hopeful as to a speedy conclusion to it.
“T have not been able to get any letters at all bearing this
year’s postmark, which is a great anxiety, as there must be
many for me at Nairobi. My life is too nomadic for them
ever to find me, and so, at my desire, they are not sent on.
I long for a return to my own researches, as life seems so
utterly empty these days.
“Tn about seven months my tour will be up, and if all is
well by then, I should be thinking of returning.”
Dr. Ta. Morrensen’s OBSERVATIONS ON THE “ FALSE
HEAD” OF LYCAENIDAE AND OTHER BUTTERFLIES, ETC.—
Prof. Poutton drew attention to “ Observations on Protec-
tive Adaptations and Habits, maimly in Marie Animals,”
published, in English, as one of the papers on Dr. Th. Mor-
tensen’s Pacific Expedition, 1914-16 (Vidensk. Medd. fra.
Dansk naturhist. Foren., Bd. 69, pp. 57-96, Pl. I), and
especially the “‘ Observations on Insects” (p. 83). The author,
@axly =)
Dr. Mortensen, had made no special study of mimicry and
his “‘ observations are made entirely independently, so to say
unintentionally, without any preconceived ideas or wishes to
find instances of mimicry, protective resemblance or the like.”
This detached attitude gave a special value to the conclusions
on the extraordinary phenomenon of the “‘ double ” or “ false
head” in Lycaenidae, reached by the author during his resid-
ence in the island of Taboga, Panama, Nov. 1915—-Feb. 1916.
Here he observed on the hind-wings the antenna-like tails,
the associated eye-spots, the alternate movements, the out-
“the most wonderful
likeness to a real broad head,” and, with all this, the incon-
spicuous real head and motionless real antennae. The
Lycaenids observed—at least a dozen species—were never
ward bent lobe of certain species giving
seen to rest head downwards but always horizontally on
leaves or flowers. The species figured were Thecla acis,
Drury, T. phaleros, L., T. battus, Cram., T. marsyas, L.,
together with four unnamed species. The Nymphaline
Gynaecia dirce, L., also figured, was stated always to rest head
downwards, usually on tree-trunks, and seeing it in its natural
position “ one cannot resist the impression that it is the head
turned upwards, and that the meaning of it must be, that
lizards are thereby induced to direct their attack at this
non-vital part.” Attention was also directed in this species
as well as in certain Lycaenids such as Thecla phaleros and
T. battus to the convergence of the lines of the under surface
pattern towards the “ false head” and the greater brightness
of the colouring near it. Hence “the eye is involuntarily
directed towards this spot. This is a curious analogy to the
honey guides in flowers.”
Although the author accepted the interpretation that
enemies are thus “induced to attack this non-vital part,
while the butterfly escapes with the loss only of a part of its
wings, unessential for the flight,” he never found a specimen
“with the false head partially or completely bitten off ’—
perhaps a consequence, as he suggests, of the limited vertebrate
fauna of so small an island; for precisely these injuries were
known to be very common, and dozens of examples from all
kinds of localities existed in the Hope Department.
(Psa +)
After his return to Denmark the author failed to observe
the movement of the hind-wings in Thecla w-album, Knoch.,
of which the false head was observed by Dr. R. C. L. Perkins
in 1888 (* Colours of Animals,” Poulton, 1890, p. 208). Prof.
Poulton had observed that the movements, which Dr. Chap-
man had aptly compared to those of the eccentricities of an
engine, only occurred under certain conditions—viz. the short
rests, generally on flowers, between flights in hot sun. Dr. ~
Perkins had kindly recalled the circumstances under which
his observations were made thirty years ago :—
** Feb. 16, 1918.
“Tt would have been on hot sunny days that I saw the
T. w-album moving the wings one over the other in the way
described, as I used to go to the place to catch a particular
Fossor on the same plant, which was a tall yellow-flowered
Umbellifer—the species I forget. It has a strong scent and
I have seen as many as half a dozen of the w-album on a
single head. The month would be July (after summer term
at Oxford). The place was a small quarry cut out in the
middle of a thick wood and a very hot place, being an open-
ing surrounded by trees, wych-elms, near Badminton, the
seat of the Duke of Beaufort, and on his estate. I went past
there a year or two ago after a lapse of about twenty-five
years and found the wood cut down and I could not detect
the quarry. I am sure I often saw the butterflies behave as
reported, and occasionally I saw one attacked by wasps
(Vespa), which frequented the same flower-heads. I have
seen other British Lycaenids make the same movements, and
also Lycaenids of most diverse kinds, in Mexico, Australia,
etc. It must be a very general habit.
“The 7’. w-album used to sit very quietly for a long time
together on one head of the flower, if not frightened. I used
to find them elsewhere in Gloucestershire and Wilts in abun- |
dance on the common small-flowered pink thistle and on
blackberry, but I cannot now remember whether I saw them
move their wings in those places. My memory is most clear
as to what I saw in that particular quarry near Badminton.”
Dr. Chapman wrote Feb. 20 and 27 :—
© xlya)
“The ‘eccentric’ appearance is due to the margin of the
opposite wing appearing and disappearing, much as one disc
of a pair of eccentrics does behind the other. It is most
remarkable as being the only case I can call to mind of the
wings of opposite sides moving asymmetrically. Wings of
opposite sides in other cases move in an identical manner.”
“T certainly associate the movements with rest in a warm
sun, but I don’t think a flower is essential. After a short
flight the butterfly settles for some seconds, hardly minutes,
apparently really for a rest, not for basking, makes these
movements whilst resting, and then goes off. The rest is a
brief interval between flights, not a rest for the night or when
the sun is obscured.”
Although as a rule the eccentric movements were performed
with the wings nearly or quite closed, Prof. Poulton felt sure
he had seen them with the wings partially expanded so that
the upper surface was distinctly visible, and he remembered
Dr. Chapman suggesting, at a meeting of the Entomological
Society many years ago, that these movements, when made
by the males of some of our common species, perhaps pro-
moted the resemblance to a blue flower slightly twisting and
untwisting on its stalk in the breeze.
The question arose as to whether the movements now ob-
served in tailless Lycaenids had persisted from some ancestral
time when tails were present—a view adopted in ‘“ Colours of
Animals,” pp. 208, 209. Prof. Poulton still thought that this
was the most probable interpretation in view of the preva-
lence of tails throughout the Lycaeninae of nearly all groups,
and the fact that the associated variations in the nervous
and muscular systems were ‘n every way likely to persist
longer than variations in colour and pattern, and in such
structural features as the tails and lobes. If this view be
correct the eccentric movements of the non-tailed Lycaeninae
had some secondary meaning, probably directing attention
to the conspicuous marginal pattern of the hind-wing under
surface which is often strongly emphasised and often exhibits
one or more eye-spots in the region of the tail even when the
tail itself is wanting; when the wings are open perhaps
having the meaning tentatively suggested by Dr. Chapman.
( xlvii_ )
And in the tailed forms secondary meanings appear to have
developed in genera such as Argiolaus, Oxylides, etc., in which
these appendages are too large and conspicuous to resemble
antennae. Mr. 8. A. Neave had informed Prof. Poulton that
the African Lycaenid in which he had been most struck by
the eccentric movements was Oxylides faunus, Drury, f. albata,
Auriv.—one of the species in which the appearance of a “ false
head” seems to have been to a large extent lost in the pro-
motion of excessive conspicuousness in the same region of
the hind-wing. It was interesting to note that the underside
pattern was such as to direct attention to the exaggerated
tails and eye-spots of Oxylides and many of its allies, no less
than to the far more perfect “ false head” of other species.
It would be of extreme interest to observe whether the
eccentric movements were ever made by the Lipteninae, or
indeed by any Lycaenid outside the Lycaeninae (in the broad
sense, as employed by Aurivillius) and Theclinae (also in the
broad sense and including all kinds of ** hair streaks’). Prof.
Poulton was inclined to believe that such movements are not
made outside these two groups and that other Lycaenids were
originally tailless. Mr. G. T. Bethune-Baker had kindly
drawn his attention to the fact that, although the Lipteninae
were always without tails, the end of vein 3 was distinctly
notched in Epitola miranda, Staud. Mr. Bethune-Baker
differed from Prof. Aurivillius in separating from the Lycae-
ninae the great, mainly Holarctic group of untailed species
as a separate subfamily, the Plebeinae, allied to the tailed
Lampidinae (boeticus group) also separated from the Lycaeninae.
The prevalence of eccentric movements of the hind-wings in
the Plebeinae was probably associated with the former presence
of tails, as maintained above.
A mode of protection analogous to the “ false head” of the
Lycaenidae had been observed by Prof. Poulton in an example
of a S. American Struthious bird, a species of Rhea, in the
Zoological Gardens at Perth, W. Australia (July 1914). When
the bird was running away it seemed to be directing its gaze
backwards at an enemy. The effect was produced by the
appearance of an eye-ball-like convexity devoid of feathers
over the ear. He had wished but had been unable to examine
(o* xlincy 9)
the appearance at close quarters and determine how far the
effect was due to form and how far to colouring. On return-
ing from the visit of the British Association he wrote to his
friend Mr. R. I. Pocock, F.R.S., who had kindly observed the
Rheas in the Zoological Gardens and had seen the same effect
insome of them. It seemed likely, however, from Mr. Pocock’s
account that the example at Perth was an exceptionally
favourable one: there was even suggested the appearance of
a dark iris on a paler eye-ball. It was quite probable that
the effect deteriorated under the conditions of captivity.
[Shortly after the above paragraph was written, the follow-
ing observation was received from Mr. C. F. Swynnerton,
writing March 29, 1918, from Chirinda, 8.E. Rhodesia. To
give anenemy the impression that its eye was upon him
would probably be advantageous to both Rhea and owl.—
“Talking of owls, I saw a very interesting thing once. I
had a live Glaucidium perlatum, an owl the size of a thrush.
One day, just after I got it, I offered it food in the forceps
through the wire of the cage. It did not take it, and looking
close, I found I was offering it to the back of the owl’s head !
The owl was asleep with its bill buried in its mant!e-feathers,
but on-the back of the head had appeared instead the
semblance of a bill and two great eyes, particularly the latter,
which were formed by two oval patches of black feathers on
the nape. I have little doubt that it is a case of mimicry,
though the resemblance is to such an owl as Syrmium wood-
fordi rather than to the Glaucidium itself. The latter is pale
round the eyes, the other dark. I sent an account of it
to the 8.A. Biological Society's Journal a long time back, but
don’t think they have yet published. My idea is that, while
it might make the Glauwcidium more liable to be mobbed, it
will be useful in relation to birds of prey; for an owl that I
tested on my carnivorous mammals proved unpleasant to them
—not, of course, that this is conclusive.”
Many other observations on insects were contained in Dr.
Mortensen’s paper. Thus it was extremely interesting to read
of the Membracid genus Sphongophorus : “I saw them often
alighting on leaves; they always fell on the side and then
looked in the most wonderful way like a small piece of rotten
PROC, ENT. SOC. LOND., I11, Iv. 1918. D
(.2°9
leaf, of which only the irregularly anastomosing ribs were
left ” (p. 85).
Mr. G. T. Beroune-Baker said that on the edge of Dart-
moor last year he took one or two Strymon w-album, Knoch,
settled on the ground in the shade with wings closed over the
thorax, and the hind-wings were quite still; again in the
same month he took one Zephyrus quercus, L., on the ground
with its wings well opened but with its hind-wings motion-
less: this also was in the shade. In both these cases the
insects were on the road, and it was well after 6 p.m. He
supposed that in each instance some shock had occurred in
the trees above and that the insects had fallen to the ground.
On the other hand, years ago at Tintagel he well remembered
watching a ¢g Polyommatus icarus, Rott., sunning itself on
the cliffs with partially opened wings and being struck with
the seemingly rotatory motion of the hind-wings, and in the
same sojourn he observed a 2 ovipositing and the same
motion occurring during oviposition. This latter poimt he
recorded in the E.M.M. for 1901, p. 227.
A mimetic AssocraTION OF ITHOMUNE BUTTERFLIES AND
A RARE Dtoptrp Motru.—Mr. W. J. Kaye exhibited, on behalf
of Mr. J. J. Jorcky, an apparently very rare Dioptid moth,
Dioptis pellucida, Warr., (Nov. Zool., vill, 438,) very imper-
fectly described from a poor specimen from Rio Dagua, W.
Colombia. Mr. Joicey’s specimen, only the second known to
us, is described as follows by Mr. Prout: This specimen of
Dioptis pellucida, Warr., is a 9 from El Tigre, Rio Jamaua,
Choco, and shows on the hind-wing a broad brown distal
border (partly worn off in Warren’s type but apparently
there duller and less broad), which brings it into beautiful
mimetic association with several Ithomiines occurring in the
same district.
Mr. Kaye contributed the following notes on the mimetic
association : The group of small Ithomiine species consisting
of Leucothyris amalda amaldina, Pseudoscada lavinia troetscha
and Hypoleria vanilia vaniliana,* nov., occurring with the
* Hypoleria vanilia vaniliana, sub-sp. nov.
Fore-wing-like vanilia vanilia except that the interspaces between the
veins are clearer and less suffused with dark smoky colour. The black
discoidal spot, apical band and margin sharper black and the five
(i)
Dioptid moth Dioptis pellucida, all having a narrow hind-wing
margin of reddish brown, is a West Colombian development of
the better-known Bogota group with a much broader area of
hind-wing colouring extending nearly up to the costa and
covering the greater part of the wing. The Bogota species in
association are Leucothyris amalda amalda, Pseudoscada lavinia
lavinia, Hypoleria vanilia vanilia and Pteronymia laura, the
last genus not being represented as far as is known in the
former group. Whether any of the species could be called
dominant in numbers it is difficult to say. None are common,
but some other species of the genus Pseudoscada are abundant,
and one might suspect in either case that the forms of this
genus were commonest.
Two other species of the Bogota or Eastern group form a
sub-group by themselves with a very heavy discal black band.
These two are Hypoleria aelia (Hew., “ Ex. Butt.,” i, nec
Hnsch. in “ Seitz,” p. 142) and Ithomia centromaculata (Wey.,
Berl. Ent. Zeit., xliv, p. 300, fig. 2). Both of these two, of
which there has been such confusion as to their identity, are
rare species, and the exact locality of either (it will doubtless
be the same for both) is not known for certain. Hewitson’s
locality for Hypoleria aelia is River Amazon, and he says in
the collection of Bates, but this is probably erroneous, and
if Bates had it, it is most likely that it came from a Colombian
locality. Of the Ithomiines surrounding the Dioptid moth
the Leucothyris (L. amalda amaldina) is the closest in pattern,
as it is the only species that has a black mark across the cell.
Wasps’ AND Ants’ Nests rrom Java.—Mr. FRIsBy ex-
hibited an ants’ nest, sent to him by Mrs. M. E. Walsh, F.E.S.,
from Soekaboemi, Java.
She wrote: “‘ This nest was found on the ground with all
the inhabitants dead. As everything was still fresh, an
accident must have happened—but what?”
The nest, which is attached to the underside of a leaf, is of
soft papery material, about 3? inches long, with the opening
white marginal spots clearer and whiter. Hind-wing with a brown
patch between outer margin and cell, but not reaching the cell.
Hab. W. Cotomsia, Rio Tamana, Rio San Juan, Choco, 400 ft.,
Feb. 1909 (G. M. Palmer) [W. J. K.].
(7 lie}
or entrance at the end nearest the leaf petiole. The ants,
which were sent in spirit, appear to be a species of Polyrhachis.
Mr. Frissy also exhibited three cells of Zethus cyanopterus,
a wasp of the family Humenidae, also sent by Mrs. M. E.
Walsh, F.E.S., from Soekaboemi, Java, and read the following
note :—
Mr. H. O. Forbes, in “ A Naturalist’s Wanderings in the
Eastern Archipelago,” figures a nest of this species, with
apparently a number of openings, which he says was com-
posed of a number of chips of leaves glued together, the
whole ‘nest being protected from rain by a projecting roof of
the same material, this roof itself being shaped like a leaf.
In the specimens I have here the cells are simple. The
question arises as to whether these cells would have been
added to at a later period, or whether this wasp sometimes
makes a communal nest and at other times only solitary cells.
LONGEVITY OF A CoLEOPTrEROUS LaRva.—The PRESIDENT
exhibited a coleopterous larva, together with the box in and
on which it had been living for some years. He said that it
was the larva of a longicorn beetle, but was unable to state
the species, and observed that similar instances of longevity
were on record. He read the following letter which he had
received with the exhibit :—
‘“ DEAR SIR,
‘] venture to send you a wooden pencil-box, which
has been badly ravaged by the larva of some boring insect,
as it may perhaps be of some unusual interest. The box has
been in my possession for many years—probably over twenty-
five, possibly still longer. The insect first made itself known
—at least six or eight years ago, possibly more—by a loud
ticking sound; so loud that it has often woke me at night,
if I omitted to place the box in a cupboard or drawer. The
sound was a clicking sound, like that of a cricket in the wall.
I am unable to say in what country it first made itself mani-
fest. The box has travelled with me widely—in India (in-
cluding the Himalayas); in the Persian Gulf, Mesopotamia
and the Turco-Persian frontier; around the shores of the
Red Sea; in Egypt, Palestine and Syria; in Arabia (down
( lit)
the Hedjaz Railway); in Asia Minor; in Greece, Turkey,
Russia and many other European countries. Until about
three months ago there was no visible sign of the insect’s
ravages; a hole then appeared in the body of the box; soon
a large amount of white powder was produced; and very
soon the box showed signs of rapid disintegration. I was
then in Southern Russia. About two or two and a _ half
months ago, while on the journey home, I found the larva
loose in the box. It is enclosed in the box, separately wrapped
in paper. Pray keep the box if it is of any interest, and in
no case trouble to return it. I should be glad to hear the
result of your observations on the larva, if it is not causing
you too much trouble.
* Yours faithfully,
“ F. G, CLEmow.
** January 8, 1918.”
JUGO-FRENATE GENERA OF MICROPTERYGIDAE.— Dr. TURNER
read the following note on Mr. Tillyard’s discovery in the
wing structure of certain Australian Micropterygidae :—
While carrying out his researches upon the Phylogeny of
the Panorpoid Orders, Mr. R. J. Tittyarp, M.A., B.Sc.,
F.L.S., F.E.S., Macleay Fellow in Zoology of the Linnean
Society of New South Wales, has made a careful study of the
Jugate Lepidoptera. The result of the study of five genera
of the family Micropterygidae (sens. lat., including the Erio-
cranvidae) is that he finds them all to be, not of the jugate
type of the Hepialidae, but of a more primitive jugo-frenale
type, in which the wing-coupling apparatus closely resembles
that of the Planipennia, Megaloptera and Mecoptera. On
the hind-wing, near the base of the costa, there is a strongly
developed frenulum of from two to six bristles (usually three
or four), which becomes engaged, during flight, in the sinus
formed between the dorsum of the fore-wing and the so-called
jugum; this latter is bent under the fore-wing with its apex
pointing outwards and forwards, and acts as a retinaculum
for the frenulum, and not in any way as a jugum or “ yoke ”
for the costa of the hind-wing, as it does in Hepialidae. The
accompanying figure will explain these points clearly. Mr.
Tillyard will shortly publish a full account of his researches,
( liv)
and only sends this short note because of the present-day
difficulties and delays in sending communications from
Australia to other parts of the world.
Explanation of text-fig.:—(a) Base of dorsum of fore-wing of
Micropteryx aruncella, Scopoli, g, to show jugal lobe (jugum) turned
under the wing. Viewed from beneath (x 120). (b) Base of costa of
hind-wing of same, to show frenulum of three strong bristles. Viewed
from above (x 120).
Appeals.
By resolution of the Council an appeal was read from the
Essex Field Club in behalf of a Pension Fund for their Curator
and Secretary, Mr. William Cole, A.L.S., F.E.S.
An appeal for subscriptions towards the upkeep of Wicken
Fen, forwarded by Mr. Rowland-Brown, was also read to the
Meeting.
Wednesday, March 20th, 1918.
Dr. T. A. CHapman, M.D., F.Z.8., in the Chair, in the
absence of the President and Vice-Presidents, and on the
motion of the Rev. G. WHEELER, seconded by Mr. Cou.in.
Election of Fellows.
2nd Lieut. Wittram Procror Smiru, F.Z.8., Haddon
House, Ashton-on-Mersey, and Messrs. Joun Henry Watson,
70 Ashford Road, Withington, Manchester, and RonaLp
(eles)
Sentor Wuirte, Suduganga Estate, Matale, of the Board of
Agriculture, Ceylon, were elected Fellows of the: Society.
Election of an Honorary Fellow.
Dr. Paut Marcnat, President of the Entomological Scciety
of France, 89 Rue du Cherche-Midi, Paris, was elected an
Honorary Fellow of the Society.
There were no exhibits.
Paper.
* Observations on the Lepidopterous Family Cossidae, and
on the Classification of the Lepidoptera,” by A. JEFFRIES
TurnER, M.D., F.E.S.
Dr. TuRNER gave an abstract of his paper illustrated by
drawings of neuration, shown in the epidiascope. Dr. Cuav-
MAN, the Rev. G. Wuerter and Mr. Bacor commented
upon it.
Wednesday, April 3rd, 1918.
Dr. C. J. GAHAN, M.A., D.Sc., President, in the Chair.
Election of a Fellow.
Dr. AttaAn Caticotr Parsons, M.R.C.S., L.R.C.P., D.Ph.,
Sanitary Officer West African Medical Staff, and Temp. Capt.
R.A.M.C., School of Army Sanitation, Aldershot, was elected
a Fellow of the Society.
Kehibitions.
BLack FORM OF PUPA OF PARARGE MEGAERA.—On behalf
of Mr. Pripraux the Secretary exhibited two black and two
green living pupae of P. megaera, and read the following
note :—
Of four larvae that have so far pupated from a few speci-
mens of this species that have been reared from the egg during
the winter, two are of the sooty-black colour, the other two
( lvi )
being normal green ones. These examples, all from 8. Devon
parents, were kept in warm rooms, and though sluggish in
cold weather, the larvae never entirely ceased feeding; they
all seem undersized, and have evidently fed up to maturity
prematurely. The colour of the pupae of between twenty
and thirty examples, reared several years ago from Isle of
Wight parents, was in every case the typical light green.
Lice AND TRENCH FEvER.—Mr. Bacort gave the following
account of experiments as to the distribution of trench fever
by lice :—
That this disease is spread by lice has been generally sus-
pected since the second year of the war, and several isolated
experiments have been recorded in which the infection has
apparently been conveyed by lice that had recently fed on
patients suffering from the disease. The number of instances,
however, was too small and the conditions not definite enough
to constitute a proof. Now, however, the work of the War
Office Trench Fever Committee in this country, as well as
that of the Joimt American-British Committee working in
France, has definitely proved that the disease is actually
conveyed by the body louse (Pediculus humanus).
In England two volunteers allowed lice that had been ‘fed
on patients suffering from trench fever to feed upon them
three times a day over a period of one month. The bites
received were about 500 per day. Neither of them con-
tracted the disease, but five volunteers, one of whom allowed
infected lice to be crushed on a scarified skin area, and four
who allowed the excreta of infected lice to be rubbed over a
scarified patch of skin, suffered from the fever. In France the
disease has been conveyed to a number of American volunteers
by lice, but the method adopted differed somewhat from that
employed here, and it is not possible to say with certainty
whether the infection resulted from the bites or contact of
excrement with abraded skin.
ANDROCONIA IN ORDERS OTHER THAN LEprpopTrEeRA.—The
Rey. F. D. Morice inquired whether androconial scales were
known in insects other than Lepidoptera. He thought that
he had discovered them among the Sawflies in the Australian
genus Perga in one species of which there was on the underside
(ivar)
of all the wings, and in several others on that of the fore-
wings only, a sort of fovea densely*packed with hairs showing
considerable structural detail. So far as he knew this
character did not exist in any but male specimens. Dr.
Dixey, Prof. Poulton and Lord Rothschild, to whom he had
shown them, agreed with him that the hairs were probably of
an androconial nature.
THE “ TAPPING’ OF ANOBIUM STRIATUM AND A. PERTINAX.
—The PrEsIDENT said that he had found the authority for
Kirby’s statement that Latreille had witnessed the * tapping”
of A. striatum with its mandibles, but he suspected there
Was some error in identification of the species. Also that
in the ‘‘ Wiss. Zeit. fiir Insektenbiologie”’ for 1910 the
Danish naturalist Jensen Haarup spoke of A. pertinax as
tapping most vigorously before a storm and being regarded
in Jutland as a weather prophet. As this was described as
taking place specially in autumn and winter, the President
considered it probable that the tapping was really made by
the book-louse.
Comm. WaLKER felt sure that he had heard A. striatum
tapping where no X., tessellatwm were present.
Wednesday, May Ist, 1918.
Dr. C. J. Ganan, M.A., D.Sc., President, in the Chair.
Time of Meeting.
The President asked for an expression of opinion as_ to
altering the time of meeting to 5 p.m., in view of the incon-
venience caused by railway restrictions, as a guide to future
action. Messrs. E. E. Green, Bacot, WiLtLouGHBy ELLIS
and TURNER spoke, and on a show of hands it appeared that
the majority would be in favour of such a change.
Bahibits.
A SERIES OF AGRIAS NARCISSUS, STAUD.—Mr. W. J. Kaye,
on behalf of Mr, J. J. Jorcey, exhibited a series of 8 3 3 and
( Ivii )
1 2 Agrias narcissus from French Guiana. He said that
from the time Staudinger described the species in 1892 till
now, the insect had remained very rare and little known,
which in the case of such a conspicuous species was remark-
able. Outside French Guiana specimens had been taken in
Surinam and at Obydos on the Amazon, but it now appeared
as if French Guiana, from whence the species was originally
described, was the real home of this gorgeous insect.
ANDROCONIAL SCALES IN SAWFLIES—The Rev. F. D.
Morice exhibited three photographs showing scales appar-
ently of an androconial nature in Australian sawflies of the
genus Perga.
Prof. Poutton, Dr. Dixry, Mr. BrETHUNE-BakeErR, the
PRESIDENT and Dr. Lonestrarr discussed the function of
androconia generally, the latter speaking especially of their
probable association with scent, especially in the Lycaenidae.
OBSERVATIONS ON THE SEASONAL FORMS OF BUTTERFLIES,
ETC., IN EX-GERMAN East Arrica.—Prof. PouLtTon said that
he had received the following interesting letter from the
Rev. K. St. Aubyn Rogers, written at Kongwa, 20 miles
N.N.W. of Gulwa Station on the Central Railway, due W. of
Zanzibar, and about 200 miles from Dar es Salaam. High
hills lhe to the south between Kongwa and the railway.
** Jan. 14, 1918.
“JT am quite sure that the seasonal forms of butterflies
would repay a good deal more research than they have yet
received. It is a very curious thing that the food-plant of
Belenois severina, Cram., etc., grows freely in the dry season,
but it is even more surprising that it does not make fresh
growth in the wet season. Moreover, this bush is also the
food-plant of Teracolus eris, Klug, as I have seen this species
ovipositing on it at both seasons. Now 7’. eris is abundant
here, and its seasonal forms are quite distinct and follow the
seasons as every properly constituted butterfly should do, so
that in its case larvae feeding on old leaves produce a wet
form and those on young leaves dry forms! !
“Our rains here began at the end of November, and we
had heavy thunderstorms on the 23rd and 27th, We had
(nlixs >}
some very light showers a week or two before. In December
we had occasional thunderstorms only amounting to about
35 ins., but this last week we have had lots of rain.
“ The first wet Precis did not appear till the end of Decem-
ber—P. antilope, Feisth., Dec. 27, and P. sesamus, Trim.,
Dec. 29, are my first records. Previously there was nothing
but much-worn dry forms, so the wet forms have a very
short season here. You will see that the seasons here are
very similar to those in 8. Africa—6 months wet and 6 months
dry, but both begin later, so that the hottest months of the
year are at the end of the dry season and beginning of the
wet season. It is very curious that Precis archesia, Cram.,
produces the limnoria, Klug, form under these conditions.
A good many Lycaenids and Hesperids seem to be confined
to the wet season.
“T was up at Kiboriani for two days last week, but the
weather was not at all satisfactory, so I did not get much.
Acraea anacreon bomba, Gr.-Sm., was plentiful and A. acrita
manca, Thur., just coming out. [have quite 30 of A. anacreon,
Trim., of both seasonal forms showing a considerable amount
of variation. During the last three days down here I have
taken 2 specimens of a form of A. acrita, Hew., or A. chaeri-
bula, Oberth. (specimen sent *), with a heavy black tip and
no subapical spots, so this form is found on the same ground
as A. acrita manca, of which I have a long series taken at
all seasons,
“On my way down I got a real prize, my first specimen of
a Mimacraea. It seems to be intermediate between M.
marshalli, Trim., and M. doherty, Roths., so far as I can
judge. I am now quite sure I missed another on the same
spot about 2 months ago.
“T have a long series of Belenois picta, Neave, but only
one specimen is like Neave’s figure of his dry form. I have
a good number taken in the dry season, but all except one
have a quite different underside. Moreover, both seasonal
forms show a good deal of variation in the amount of black
* Determined by Dr. H. Eltringham as A. acrita ambigua, Trim., 3.
Dr. Eltringham considers it very interesting that this form, originally
described trom N. Rhodesia, should have occurred in the area of A.
acrita manca.
( Ix )
at the apex of the fore-wing, and in some specimens it is very
much reduced, and the subapical spots of the underside of
the fore-wing are in some cases quite obsolete.
*“ The Charaxes etheocles, Cram., I took at Mamboya was
2 form phaeus, Butl. [mimicking the 3 of Ch. bohemanni,
Feld.]. I enclose a small piece of food-plant of the Argiolaus
I wrote about. I have little doubt that it is A. silarus,
H. H. Druce, but it is remarkable that it is so common here,
as I believe it is generally a rare species.”
Prof. PouLTon said that he had sent the piece of Loranthus
to Dr. Otto Stapf of the Kew Herbarium, who had kindly
written : “* The Loranthus you sent is probably a new species
closely allied to L. proteicola, Engl., from the Kinga Moun-
tains. I have not been able to match it exactly with any of
our specimens. L. proteicola has been collected only once,
and we have merely a fragment of it. I can therefore not
say what its range of variation is, and whether your specimen
may not come after all within that range. Mr. Sprague,
who has monographed the African species of Loranthus—over
200 species in tropical Africa alone—is at present in India on
military duties.”
THE CONFIRMATION OF Dr. R. C. L. PERKINS’ CONCLUSION
THAT THE EARLY PALE SPRING FORM OF PARARGE AEGERIA, L.,
RACE EGERIDES, STAUD., IS PRODUCED FROM OVER-WINTERING
pupAE.—Prof. Poutton exhibited the specimens of egerides
collected and bred by Dr. Perkins in 1917 together with the
1918 material, which confirmed the prediction published last
year (Ent. Record, vol. xxix, p. 202, 1917). The former
series had been kindly handed to him by Mr. H. J. Turner,
who had exhibited it at the South London Entomological
Society. The interesting evidence obtained in the present
year was described in the following extracts from Dr. Perkins’
letters and in his note :—
“ April 5, 1918.
‘In a few days now I shall, I hope, be sendmg you the
new lot of ‘ Speckled Woods’ bred from over-wintered pupae.
I had very few of these pupae, and of these two died, one
produced a cripple, and one shows no sign of hatching. The
Cat ©)
series consists of 14 examples only, but they are quite enough,
and I think you will find when you place them alongside of
my last year’s “ over-wintered larva’ lot, bred last spring,
that they will quite confirm my conjecture that the * early ’
or ‘ pale spring form’ is produced from wintered pupae, and
the ‘late’ or ‘dark spring form’ from wintered larvae. I
feel quite pleased at reaching a conclusion, as it has taken
me three years to do so.
“One of the 2 2 of this lot is quite a lovely thing, finer, I
think, than that very nice one (in the pale spring lot) that
I caught at Teignmouth last year. It is the most extreme
form I have seen. The other chief point of interest, which
remains an enigma and which | cannot solve by experiment,
I can guess at the solution of. In several years | have noticed
that although the light spring form antedates the dark one,
yet before, and even considerably befcre, the first ight form
is seen at large, one or two dark specimens, closely resembling
the dark spring form or the 2nd or summer generation of the
butterfly, will be taken. I feel quite sure these are from
over-wintered pupae also, but that these pupae are ones which
should have hatched, to form part of the summer brood of the
previous year. A year or two ago | had pupae from spring
butterflies (the larvae pupated in July) which had not hatched
in early November, but when brought indoors into a more or
less heated room they produced butterflies that month. These
would never have hatched out of doors till the spring, and I
feel sure the few dark, very early specimens belong to this
class. Probably it largely depends on climatic conditions in
different years whether any of these or how many are seen
in the sprmg. I took one in a Paignton lane this year on
March 24th, and a torn one (which must have been out a
week or more owing to the bad and cold weather we have
had) to-day. Also to-day the first specimens of ‘the pale
spring form” were out in the lanes, but I don’t suppose there
will be any of the true ‘dark spring form’ (from wintered
larvae) for 3 or 4 weeks yet, although the grass is now in
splendid condition, and when this becomes really nutritious
after the winter the caterpillars grow pretty quickly with
good weather.”
( Ixii )
“* April 16, 1918.
“In addition to the 15 aegeria, bred from over-wintered
pupae, I am sending an example of the first wild spring form
seen in 1918, one of several met with in a very short walk.
It is a g, captured on April 5, the day on which one of the
bred males emerged. They are very considerably like each
other. I also send a dark wild male resembling a 2nd brood
(summer) form. As referred to in the accompanying paper,
it probably 7s a 2nd brood specimen, which, owing to retarded
emergence, has over-wintered as a pupa, and should have
been a last summer’s butterfly.”
FURTHER NOTES ON PARARGE AEGERIA, RACE EGERIDES, BY
Dr. R. C. L. Perxins.—With butterflies which emerged at
the end of August 1917 (these being part of the summer
brood bred that year), pairings took place in the cages and
eges were laid from the first to the third week in September.
As the weather became colder the larger caterpillars were
placed in the warmest situation procurable (but not exposed
to any artificial heat), and fed on the most luxuriant grass.
In spite of this, many of them grew very slowly indeed, and
consequently, there bemg no chance of their pupating, these
were liberated, as had been already done with the greater
number of the smallest larvae obtained from the September
egos. Highteen pupae in all were obtained at the end of
October or early in November. It was a noteworthy fact
that of the 18 caterpillars from which these resulted, not one
pupated on the growing grass within the cage, but all left
this and attached themselves to the dry bark of the uprights
or crosspieces that supported the covermg. In this respect
they contrasted very strongly with the pupae obtained in the
early summer, for a large proportion of these were attached
to the blades of grass. Also some of these winter pupae were
extraordinarily dark, appearing almost black to the naked
eye before the emergence of the butterflies. Two pupae died
during the winter and one produced a cripple, the butterfly
having, on emergence, fallen from the pupa-case, to which it
was clinging, on to the damp earth beneath. The other 15,
except that one or two were insignificantly damaged by
: @ isa >)
fluttering in the cage, were perfect specimens, several indeed
might be called; beautiful.
The reason why these pale spring forms are, all but two,
ahead of the wild ones is because they were treated exactly
the same as the last year’s dark spring forms, or some of
these. The pupae were exposed in their cage to the outside
air in an eastern aspect durimg the (comparatively) severe
weather of the past winter, but on February 18th four were
brought into my study, where there was the usual tempera-
ture of a room heated through the day from an open fireplace.
These four produced butterflies on the 6th, 8th (2) and 9th of
March, all being males. The rest of the pupae were brought
indoors about March 7, some already showing slight signs of
approaching emergence, and the butterflies appeared from
March 23rd to April 8th. Counting the crippled example,
above alluded to, six in all were females. Although I have
no specimens of my previous captures or bred examples for
comparison, it seems clear to me that this bred series belongs
early” or “ pale” sprmg form
ce
to what I have called the
of egerides, and that my supposition, that this form must be
the produce of over-wintered pupae, is correct.
There is, however, still one point in connection with the
spring butterflies that I have not alluded to. Even earlier
than the * pale spring form ”’ in several years I have noticed,
as a rare occurrence, the appearance of casual dark specimens,
that look quite out of place amongst these more conspicuously
spotted ones. A dark example of this sort I caught im a
lane near my house on March 24th this year, and a tattered
specimen, that must have been out for a week, at the beginning
of April. The first wild specimens of the “ pale” spring form
were seen (several in half an hour) on April 5th, and these
quite resembled my bred series. The occurrence of the very
early dark butterfly is, I believe, to be explained in this way.
In some seasons I have every reason to believe that some of
the pupae that would normally result in a second brood fail
to do so, and remain over till the following spring and then
produce these dark butterflies, which much resemble some
males of the 2nd or summer generation. One year, pupae
that were obtained by me in July from spring butterflies had
@ Axes}
not yielded imagines at the end of October, but on being
brought indoors produced these early in November. Had
they been left out of doors they would certainly not have
hatched till the following spring. Consequently in 8. Devon,
so far as I can judge from three years’ experience of breeding
specimens and from special observation of living specimens,
as well as from more general observations of these during
earlier years, the following facts seem to be true :—
(1) There are always or generally two forms of the spring
brood of egerides, a lighter (earlier) and darker (later) one.
(2) The former is from over-wintered pupae, the latter from
over-wintered larvae.
(3) In some seasons a dark form appears even before the
lighter (earlier) spring form, and probably results from pupae
which normally should have hatched (as a second brood)
during the preceding summer, but have failed to do so.
(4) As the spring forms overlap in their time of appearance,
no doubt interbreeding between them takes place.
(5) No definite tendency to dimorphism, such as is seen in
spring, has been observed in the second generation.
(6) Owing to the facts stated above, perfectly fresh examples
of the spring butterflies can be found from March till well
into June, the later ones not being a second brood, but the
imagines from larvae that have hibernated, when still very
small. It follows from this that the true second or summer
brood is likewise very protracted.
(7) Whether there is a third brood, except as an entirely
abnormal occurrence, is doubtful, at least under natural
conditions,
(8) The second brood specimens resemble the darker (later)
spring form rather than the earlier one.
How far these observations apply to the butterfly in other
localities I do not know, but in Somerset and Gloucestershire
I do not think the facts will prove greatly, if at all, different.
A FLIGHT OF WINGED TERMITES AT BARRACKPORE.—Prof.
PouLTon said that he had recently received the following
letter from Mr. G. A. James Rothney, referring to Dr. G. B.
J? o
Gal)
Longstaff's note on p. 37 of Shelford’s ** Naturalist in Borneo ”
(London, 1916) :
* Page 37. Termites.— The flight of the Winged Termites
is a great event in the animal year.’
“T can fully endorse this. I have had several flights of
Termites in my different bungalows at Barrackpore, but one
in particular at 33 Park Road is worthy of record. The
bungalow was raised on low arches. These were bricked up
and ventilations left, and various jungle animals— Janwar ’—
used to scrape out the ventilators and use the arches as a
sleeping abode.
“One night in the Rains a big flight of Termites took
place in the corner of my dining-room—they came out from
the brickwork in thousands, shedding their wings all over the
place as thick as leaves in a winter storm. I was soon driven
from my dinner table, as dishes, plates and glasses were soon
filled with them. Very soon—a few seconds it seemed—the
following collection of * Janwar’ appeared on the scene, all
devouring white ants :-—
“1. Bats—in numbers, several species hawking them about
the room.
‘2. Lizards—on the wall and floor, shikaring them.
“3. The Indian Crow—picking them up right and left.
‘4. The Indian Mynah—picking them up right and left,
but more gently.
** 5. A Musk Rat.
“6. The Indian Cockroach.
‘ All the above within the dining-room.
‘In the verandah within the sphere of light :
‘7. Pariah Dogs—several.
‘8. Jackals—several.
‘9. Jungle Cats—several.
¢
©
10. Mongoose—two.
‘On the steps of the verandah :
‘11. Bull-frogs—several.
“And outside in the Compound in the half-dark were
certain other ‘ Janwars’ of sorts that appeared to be Civet
Cats of some kind, and an uncouth figure looked like a
PROC. ENT. SOC. LOND., III, IV. 1918. E
( dxvi })
Hyena. The nuisance became so great that I was driven to
my bedroom to seek the protection of the mosquito curtains
with the lights turned low, and in Biblical language ‘ they
took up of the remains several baskets full,’ that is, the
* Mehter “—sweeper—in the morning swept up a huge quantity
of wings. [have experienced several incidents of this character,
but this was a real ‘ Brock’s Benefit ’ in White Ants.”
Messrs. NEAVE, GREEN and Bacor commented on the
edibility of Termites.
BRITISH CAPTURES OF POLISTES GALLICA, L.—Prof. PouLTON
said that he had received the following note from Mr. G. A.
James Rothney, referrmeg to the captures of Polistes gallica
reported in the Entom. Proc. for 1916, pp. Ixvi, Lxvii :—
“The following note may be of some interest. Charles
Horne, B.S.C., of Mainpuri, the author of a jomt paper with
Frederick Smith on ‘ Aculeate Hymenoptera of the N.W.
Provinces, India,’ is reputed to have captured Polistes gallica
in the West of England in 1870-71. Frederick Smith told me
of the capture in 1871, and evidently believed in its being
genuine. He showed me at his house, 27 Richmond Crescent,
Islington, a box of captures of English Aculeates made by
Horne. JI remember it distinctly; it was a rough square box
of Indian make, and in one corner were several specimens of
Polistes gallica—said by Horne to be English. Frederick
Smith evidently believed in Horne’s statement. At the same
time he wished to follow it up further in case Horne might
have mixed his English with Continental captures, as he had
been staying on the Content. Horne was quite positive
about their being English and West of England—either Devon
or Dorset. Frederick Smith arranged with me to go down the
following year, 1872, to search for it thoroughly, and pro-
mised me he would get further particulars of the exact locality
from Horne. It was a general custom with Frederick Smith
to follow up his lead in this way, when his own Museum
holidays would not permit his visiting the locality at the
right time, as in the case of the sexes of F. exsecta at Bourne-
mouth in 1868, but in Feb. 1872 I left for India, and the plan
fell through.”
(* xvi”)
Prof. Poutton said that Dr. ‘R. C. L. Perkins, who pos-
sesses the F. Smith British Aculeates, had informed him that
the collection contains 4 Polistes gallica of both sexes, with
the note beneath them in Smith’s handwriting: ‘* Mr. Horne
thinks that he took it near Swanage (Dorset)? ?”’ The exist-
ence of these specimens was recorded by Dr. Perkins in E.M.M.,
1917, p. 229. Dr. Ferkins had written: “I suspect Polistes
gallica has been not infrequently brought over with shrubs
or in other ways, and has once in a way started a colony
only to be sooner or later exterminated by our climate. Three
species of Polistes (one American and two Oriental) have
become fully established in the Hawaiian Islands from acci-
dental importations, and many specimens of a 8. American
species were brought in steamers to England (1866-1869).
These also are in F. Smith’s collection.”
GIANTISM IN MALE BEES.—Prof. PouLtron exhibited the
illustrative specimens and read the followmg paper for Dr.
R. C. L. Perkins, who, he much regretted, was unable to be
present. Extracts from two letters by Dr. Perkins threw
further light on this interesting and difficult problem, and
explained how Dr. Perkins came to study it.
** March 13, 1918,
“A few years ago, when writing my unpublished account
of Andrena and its parasites, I puzzled much over the giant
males, and could think of nothing but the suggestions I have
written in the accompanying note. It seems very curious
that neither Saunders nor Smith nor any others, so far as I
know, seem to have paid any special attention to this subject.”
“ April 16, 1918.
“T begm to think that difference in size of Andrena must
be somehow due to the amount of food. It is very hard to
investigate the matter here. I got out about a dozen cells
of Andrena clarkella, Kirby, the other day, and all the pollen
lumps appeared to the naked eye about the same in size.
When my boys came home and saw these they both exclaimed
at once, ‘ What small lumps, much smaller than the ones we
got the other day ! —from a neighbouring colony. They did
(- Ixvant >)
not bring these home, but I feel sure they were right. Still,
I cannot understand the uniform size of the 99. The 33
are all sizes, with occasional gigantic ones. The 99 all uni-
form in most Andrena, with very rarely one about half the
proper bulk.
* The most favourable (7. e. for variation) species to investi-
gate do not make compact colonies like clarkella, but burrow
singly, scattering over perhaps a whole field—I mean the
favourable species in this locality. A very easy one to inves-
tigate would be A. fulva, Schr., which produces gigantic 3 3
freely in ‘the Parks’ at Oxford and makes big colonies, but
unfortunately it is not here at all. Also our soil is not very
easy to dig in—an extraordinarily wet clay at the roots of
trees, where the clarkella were nesting.
“ T may chance on some better colony soon. I badly want
larvae of the bees Nomada (parasitic on Andrena). No one
knows whether both host and parasite lay eggs on the same
pollen mass, and the latter larva kills the other, or what
happens. The want of exact information as to the habits of
the cuckoo-bees is simply astonishing.”
Giantism in Male Bees, by Dr. R. C. L. Perkins.
No one who has examined a considerable collection of bees
of the genus Andrena—or, in fact, of some other genera—
can have failed to notice the occasional occurrence of indi-
viduals of the male sex of gigantic size. This giantism has
been observed by me in nearly all our British species of
Andrena and probably occurs in all. Great variation in size,
whether this be in excess of the average or in decrease, is of
course a very familiar phenomenon in many insects, but
owing to the nature of the nutriment of the larvae and the
manner in which this is provided, it is of particular interest
in the case of the solitary bees. So far as we know the
amount of food stored in the bee’s cell to serve as food for
the larva varies little, though certainly it is desirable that
accurate investigations should be made on this point. At
the same time the comparatively uniform size of the females,
excepting in special cases to be noticed, confirms the impres-
sion made on me by the examination of actual stored pollen
G Vix)
masses, that the mass of food stored is not subject to much
variation. As just stated, the size of the female of a species
is not very variable, except as a rare occurrence, and this
rare variation appears always to consist in great diminution
of size, so that the individuals affected are comparatively
dwarfs. In looking through a large number of such indi-
viduals I find that these dwarfs appear, as far as one can
judge, to be about half the weight of normal examples, and
one is led to suppose that they are produced from two eggs
having been laid in a single cell of the bee, a fact which is
known to take place in some instances.
The variation in the males is less regular, dwarfs occur as
in the females, and specimens both notably above or below
the mean size are frequently observed, but amongst these
there stand out conspicuously the giant individuals, as a
phenomenon quite distinct from anything observed amongst
the females. We may note that these huge males frequently
approach closely in bulk that of the average-sized female,
but it is a matter of great doubt how they are produced.
It can hardly be a question of a simple surplus over the
usual amount of food, since gigantic females do not occur,
unless we suppose that the surplus nourishment goes to form
superior size in the case of one sex and some other develop-
ment in the other. This is not inconceivable, since we know
that the drain on the strength of Andrena by the parasite
Stylops is such as to cause almost invariably, if not always,*
a degeneration of the ovaries in the females, these organs
requiring much nutriment, while in the males, according to
my own observations, practically confirmed by those of
Geoffrey Smith and A. H. Hamm, little or no degeneration
of the comparatively small genital glands is produced. Con-
sequently a surplus of food might in the case of the females
be used up in the nutriment or growth of the important
ovaries, while this might be used for a general increase in size
in the males.
We know, from observations on cells superimposed one on
the other and with only one exit, that the eggs which will
produce males and those which will produce females are not
* According to the observations of Geoffrey Smith and A. H. Hamm.
(TABS s)
laid indiscriminately, but, when both sexes are present, that
the upper cells produce males, which emerge first, the lower,
females, which emerge later, and it is conceivable that the
food supplied to these cells is different in some respects. A
male bee in such a case might conceivably be changed in
size, 1f bred on food normally supplied to a female, but there
is no evidence that the food in different cells of one species
varies in quality, although the proportion of pollen to honey
varies greatly in the case of different kinds of bees.
The following facts seem to be almost or quite constant :—
(1) Giantism is only exhibited by the male sex.
(2) Truly gigantic males are a very small percentage of the
total number of individuals.
(3) A gigantic male may be taken from the same burrow as
normal ones.
(4) There is no striking development of secondary sexual
characters in such males. Thus when there is a special tooth
on the mandibles, or the cheek is armed with a special spine
in the male, these do not undergo any extraordinary develop-
ment in gigantic individuals. There is, for instance, no
change comparable with that exhibited by the teleodont and
other forms of Lucanid beetles or in the horns of Dynastids.
(5) Though they approach the normal female in bulk, and
consequently in some cases somewhat resemble that sex in
superficial appearance, there is really no accession of female
characters in any respect.
(6) They fly with and behave like normal individuals and
appear perfectly healthy.
(7) The presence of the parasite Stylops does not necessarily
prevent giantism, as gigantic males have been found containing
this parasite.
THE PAIRING OF STYLOPS AND “ ASSEMBLING” OF THE
MALES OBSERVED BY Dr. R. C. L. PerKins.—Prof. Poutron
said that he had received the following three letters and the
accompanying specimens and drawings from Dr. Perkins, who
was unfortunately unwell and unable to be present and give
an account of his most interesting and important discoveries.
All were written at Paignton, S$. Devon.
Proc. Ent. Soc. Lond., 19178. Plates A
Half-Tone Eng. Co. Ltd.
STYLOPS ATERRIMA male (legs omitted) IN COPULA
with female.
“ April 22, 1918.
“T think the following may interest you, as I believe I
told you I was taking exception to Geoffrey Smith and
Hamm’s conclusions (in the Quart. Journ. Microscop. Sci.,
vol. 60, Pt. 3, Sept. 1914, p. 435) as to the impossibility of
fertilisation of 2 Stylops and the uselessness of the ¢ ¢! In
the continuation of my papers on Stylops in HE. M. Mag. (1918,
pp. 67 and 73) I have given strong arguments of a theoretical
character against these conclusions, but this morning at
8.30 a.m. I bred a 3 Stylops aterrima, Newport, and soon
afterwards obtained an evident pairing between it and a 9.
It is curious that I should have succeeded at the first attempt.
I was astonished at the extraordinarily rapid manner in
which coupling was effected. Twice the 3 Stylops was brushed
oft by the bee (Andrena trimmerana, Kirb.) before it properly
mounted it, but the third time it got fairly on and in a second
or two was coupled with the minute projecting part of the ¢.
I had to carry it to another room and find a cyanide bottle
to kill it, so that it remained coupled in life for probably
1-2 minutes, and in addition it took say 30 sec. to 1 min.
to kill the bee. In spite of this, it still remains attached to
the @ in the manner shown in the sketch, reproduced in
Plate A. :
‘ob. pl. is the (generally reddish) oblong abdominal apical
ventral plate of the 3, from which the aedeagus may be seen
entering the * brood opening’ b. op. of the 9 cephalothorax
(v. e. really an opening between head and thorax).
“m. is the rudiment of the mandible of the 2 puparium
(for of course what one sees is not really the actual 2 but
the puparium in which it lies).
“ap. m. is the apical margin of the bee’s 4th segment, from
beneath which the 9 cephalothorax projects.
* The cephalothorax of the 2 Stylops is seen from the side,
so that only one of the mandibular rudiments is visible.
‘* The drawing was made in lateral aspect by camera lucida
many hours after death, so that contraction of the long
slender 3 body had taken place.
“Tf the g Stylops does not become detached in the great
(Gab. S.ati 59)
contraction that takes place in drying it might be worth while
exhibiting im situ on the bee.
“The 3g Stylops is in lateral view, the legs are omitted,
only the left antenna and maxilla (or palp), the clavate (rudi-
mentary) front wing or elytron and the hind-wing being
shown.”
April 24.—* This morning, though changed in position from
great contraction of itself and also partly from that of the
Andrena, the 3 Stylops was still attached to the 9. To-night,
on taking it out of the box, it became detached, no doubt
from the slight jerk caused by withdrawing the bee’s pin
from the cork. I have therefore mounted it on card in such
a way as to give a good enough view of the pick-like aedeagus
in some aspects. I have no other specimen of this Stylops
so satisfactory for examination, though I shall not have time
to make preparations of parts till after you exhibit it, if this
is now worth while.
* The bee from which it emerged contains the 2 with which
it copulated, so they may be brother and sister.
“When the fog cleared at midday to-day and the sun
shone brightly, I went up to the Stylops locality. I did not
get any 3 S. aterrima, indeed it is now late for that here, but
immediately I got to the place, where (it being entirely shel-
tered from the E. wind) it was very hot indeed, I saw 2 3
Stylops hovering close to a very dense and stiff flowering
head of gorse. I netted these, hittmg the bush in doing so,
and found a number of Stylops in the net! While I was
boxing the first (they were extraordinarily wild and active in
the net and difficult to box), I distinctly saw one or two get
out through the meshes of the mosquito net which I use for
bees, and I know not how many escaped. Anyhow I secured
4 fine specimens. I cannot doubt these 3 3 were ‘ assem-
bling,’ for in two long hours along that hedge of gorse I saw
no other specimen, and in the thousands of bees that were
out I saw only 3 stylopised individuals.
“One of these 4 3 3d paired with a 2 on my return home,
but it parted or the bee got rid of it before I could kill them.
This species was Stylops wilkellae, Perkins, a species exces-
sively close to S. melittae, Kirby, that Hamm investigated.
( Ixxiii_)
“T expect the has to be very fresh to attract the ¢ 3, for
if not fertilised the eggs start developing parthenogenetically,
and then probably she will not call the 3 3.”
© April 27.
* T have to-day had another go at Stylops in the field, and
this will probably complete my observations for this year, as
most of our Stylops are now. over for the season.
“ On the 25th I took my eldest boy to Churston, between
here and Dartmouth, as Andrena nigroaenea, Kirby (host of
Stylops melittae—Ceoflrey Smith’s and Hamm’s _ species,
common in the Parks at Oxford) is commonly stylopised
there. Unfortunately we only found a few, from which the
3 Stylops had emerged, and some with 2 9, and we saw no
Stylops on the wing. However, my fever was still high and
the sun was very hot, and consequently I had to sit down in
the shade for a considerable part of the few hours I was
out.
“On the 26th I did no Stylops work. To-day I started
about 9.30 (7. e. 8.30 a.m. old time) to the Stylops field near
my house. The gorse hedge was still partly in shade and
the grass very wet with the heavy dew, but at the very same
bush where I found the other ‘ assembly’ I saw one or two
Stylops hovering and struck at these. I boxed 6 3 3 from
this stroke, and some escaped through the meshes! One of
these I caught in my hat as it flew off (this being included
in the 6). This was about 10 a.m. (9 a.m. vere). I saw no
more for more than an hour, when at the other extremity of
the long field several were seen hovering above and behind
the gorse (which forms the front of the hedge) about a lot of
briars and brambles. On a dead stiff stem of briar I saw a
space of several inches absolutely white with a moving mass
of 3 Stylops just close to where the others were hovering.
I struck at these, but got hopelessly caught up in the thorns,
and I could see many of the Stylops escaping from the net.
When I got free, | boxed 7 3 out of the net, and still some
others escaped through the meshes. I distinctly saw a
stylopised Q Andrena wilkella, Kirby, fly heavily off when I
struck at the Stylops on this occasion. There could not
( ‘borg 4)
possibly have been less than 50 3 Stylops in the original
assembly, but when I looked up after boxing the 7 (which
took some minutes, as they are so wild in the net) I could
see no trace of any remaining. At about 11.45, having seen
no more, I went away from the hedge into the field to see if
any 3 Stylops might be seen about the burrows of A. wilkella,
and if the bees themselves were in any numbers. So far I
had only seen two of the Andrenas on the hedge—both
stylopised. The burrows did not appear numerous, being
scattered over most of the field, one here and one there, and
not forming a compact colony, such as I have often seen in
the sandy lanes near Shotover. I captured every wilkella I
saw, 26 in all, of which 25 were stylopised and 1 ¢ bee only
healthy !
“It must not be supposed that practically all the A.
wilkella in the field are stylopised—there is a strong tendency
for stylopised examples to emerge a week or even two weeks
before the average date of appearance of the healthy ones.
Therefore one may go to this field a fortnight hence and very
likely get plenty of healthy and very few stylopised ones.
Also stylopised bees are much easier to catch than healthy
ones. For this reason the percentages of stylopised to healthy
bees given by various authors on particular occasions is of
very little real value.
‘Except in one case all the 25 stylopised bees contained
either 2 Stylops or empty puparia of the g. One contains a
full 3 puparium, but the protruded part of this is daubed
over with a patch of the red soil, which has prevented the
emergence of the insect. I took several of these stylopised
bees and placed them in slightly opened boxes in the gorse
bushes, but nothing was attracted, as I had hoped might
happen. While collecting these bees, I saw a single 3 Stylops
pass high overhead (I could not reach it with my net, which
was on a 3 ft. stick) in the middle of the field, flying straight
across, but I lost sight of it after a while.
At 1.15 p.m. (12.15 vere) I captured a 9 wilkella contain-
ing 2 2 Stylops more than usually extruded. I held this in
my hand by the head and thorax with the abdomen fully
exposed to the sun. Within five or six minutes I caught
(aime ©)
5 3 Stylops flying about 3 ft. above the grass towards me,
and one other escaped, being carried off by a sudden and
rather strong puff of wind. Whether these were actually
attracted by the 2 Stylops I had had in my hand I do not
know, but I strongly suspect that they were.
“Tt is extremely probable, I think, that the 9 Stylops at
a certain (perhaps very brief) period of its life is highly
attractive to the 3. It is quite possible that this attractive
stage may be sometimes lost before ever the bee leaves the
burrow, and in that case the eggs develop parthenogenetically.
“Tt is noteworthy that on this lovely summer-like day,
from 9.45-1.15 being spent in the Stylops locality, only one
3 Stylops was seen singly, all the others were actually in
‘assemblies’ or flying in one direction and one after the
other, as if to form one.”
Dr. Dixey commented on the physiological significance of
giantism ”’ and its possible cause.
oe
Paper.
The following paper was read :—
“The Charina group of Pinacopteryx,”’ by F. A. Dixry,
M. Ay MED ER is4 Pa.S:
Dr. Dixey illustrated his paper by the exhibition of specimens.
He pointed out that this assemblage of species or subspecies
differed from the remainder of the genus by the character of
its scent-scales, and also, as had been noticed by Dr. Eltring-
ham, by the possession of a single posterior spine to the
clasper instead of two spines as in the pigea section of Pina-
copteryx. The uncus also exhibited distinctive features. The
various forms included in the group might be most con-
veniently ranged under the followmg heads :—
1. P. charina, Boisd., inhabiting Cape Colony, Natal and
the Transvaal.
2. P. simana, Hopfi., originally described from Mozambique,
and occurring throughout Rhodesia, Portuguese and “ Ger-
man” East Africa, British East Africa (with the exception of
the district surrounding Mombasa), and Uganda.
( Ixxvi )
3. P. liliana, Gr. Smith, the form peculiar to Mombasa and
the immediate neighbourhood.
4. P. gerda, Gr. Smith and Kirby, a form closely allied to
the preceding, but separable, and inhabiting an adjacent
region of British Kast Africa.
5. P. venata, Butl., originally described from the White
Nile, and found also in Abyssinia, Southern Kordofan and
the Southern Sudan.
The type of P. doxo, Godt., belongs to this group, but being
a female of unknown locality and in bad condition, it cannot
be determined with certainty. The forms above mentioned
are probably best regarded as geographical subspecies; at
present they appear to be distinct, but further information
may show that they intergrade in certain localities.
Wednesday, June 5th, 1918.
Dr. C. J. Ganan, M.A., D.Sc., President, in the Chair.
Election of a Fellow.
Mr. Ausyn R. D’ALBREU, 3rd Divisional Signal Company,
Mesopotamia Expeditionary Force, was elected a Fellow of
the Society.
Proposed Alteration of Bye-law.
The Secretary announced that it was proposed at the
request of the Treasurer to amend Chapter VIII, clause 5,
as follows :—
The Council shall nominate a Chartered or Incorporated
Accountant annually who shall audit the Treasurer’s accounts.
The Auditor shall be paid a fee, the amount of which shall
be agreed by the Council on behalf of the Society. The
Treasurer shall furnish the Accountant with all the facilities
he may require for auditing the Accounts.
C ixxvin.)
Exhibitions.
PuPATION OF TIMARCHA TENEBRICOSA.—Mr. HuGH Main
exhibited subterraria with larva and pupa of Timarcha
tenebricosa, and called attention to the colour of the pupa,
which was similar to that of the red fluid emitted by the
imago, and of the ova and newly moulted larvae.
A DIPTERON NEW TO THE BritisH List.—Mr. J. E. CoLiin
exhibited specimens of Humerus tuberculatus, Rdi., a Syrphid
new to the British List of Diptera; also specimens of Humerus
strigatus, a species under which it may easily have been
placed in collections. Both species had been reared by
Mr. J. C. F. Fryer from larvae found in Narcissus bulbs
grown at Taplow (Bucks.). ;
He pointed out that though F. strigatus had been recorded
from the Continent as attacking onions and potatoes, in
addition to Narcissi, no such attacks had been noted in the
British Isles, indeed at Taplow onions grown between the
rows of the infested Narcissi remained uninjured. In 1917,
however, Humerus larvae were found in a previously un-
recorded food-plant, viz. parsnips, grown in the Evesham
district of Worcestershire, and the specimens of EL. strigatus
exhibited were some of those reared from these larvae.
The headquarters of the genus Humerus is the Mediterranean
region, and ££, tuberculatus is an Italian species which has
remained unrecognised ever since it was originally described
in 1857.
THE MODERN USE OF THE WORD “ CAMOUFLAGE.’’—Prof.
PouLTON said that he wished to enter a mild protest against
the modern use of * camouflage ” for Protective and Aggressive
Resemblance (Procrypse, Procryptic, and Anticrypse, Anti-
cryptic). “* Camouflage ” did not appear as an English word
in Murray’s Dictionary, but ‘* Camouflet ’’ was in use in 1836,
with the following meaning :
* A mine containing a small charge of powder, placed in a
wall of earth between the galleries of besieged and besieger,
so as, in exploding, to bury, suffocate, or cut off the retreat
of the miner on the opposite side; a * stifler.’
* 1836 in Penny Cycl. VI, 197/1, Camouflet or Stifler.”
( ixxvin )
“ Camouflage ” might therefore be properly used for the
defensive discharge of the Bombardier Beetle and many other
Carabidae, and for the use of suffocating or irritating secretions
generally, but was a most inappropriate term by which to
express a concealing coloration.
BuD-AND-FLOWER-LIKE FLATIDAE (HOMOPTERA) FROM EX-
GERMAN East Arrica.—Prof. Poutron exhibited beautiful
examples of the green bud-like Ityraea speciosa, Melich., and
the many-coloured flower-like J. nigrocincta, Walk., collected
by Mr. A. Loveridge at Mrogoro, on the Central Railway,
about 100 miles W. of Dar es Salaam; also specimens of the
orange-red, flower-like J. gregoryi, Dist., taken at Kibwezi,
British East Africa, by Mr. W. Feather. All these specimens,
which had been kindly sent by Mr. E. C. Chubb of the Durban
Museum, were bright and fresh and gave an unusually striking
impression of the bud-and-flower-like appearance.
The flower-like ngrocincta were, in the resting position,
scarlet anteriorly, passing into a narrow zone of orange
followed by a broad one of very pale blue, and this by «
still broader terminal area of very pale ochreous. The fore-
wings of the green speciosa were encircled, except near the
hinge, by a narrow red line enclosed within a narrow marginal
black one, with a much stronger development of both red
and black on or near the costal border, accompanied by
bright yellow markings and a vivid bluish green modification
of the ground-colour. In spite of the obvious differences
between the patterns there were resemblances between the
black markings which suggested, as Mr. Loveridge believed,
that they were the dimorphic forms of a single species; and
the same element in the pattern rendered it probable that
the more northern gregoryt was the flower-like form of another
dimorphic geographical race of the same species, separated
from the southern race by colour differences only.
Among other interesting observations on the Ityraea made
in 1917-18 in the ravine of the river at Mrogoro, Mr. Loveridge
noticed that the green forms were much rarer—at first about
1 to 11, later 1 to 10—and much easier to catch than the
blossom-like forms. The latter were often found im cop. :
once the two different forms were thus taken, and on the
( eax”)
same oceasion a green pair and a blossom-like pair were also
captured in cop. Mr. Loveridge also took individuals exhibit-
ing a gradation between the two forms. With this evidence,
and especially that furnished by the pairing of the different
forms, there could be no reasonable doubt that Mr. Loveridge
was right in concluding that the Mrogoro forms were the same
species.
A full account of the observations had been communicated
by Mr. Loveridge to the Zoological Society of London. It
should be added that neither Mr. Loveridge nor Mr. Feather
had seen the insects arranged in the manner represented by
Prof. Gregory in “ The Great Rift Valley,” an arrangement
which, however, had been confirmed by other naturalists.
S. Nigerian LYCAENINAE BRED FROM LARVAE FEEDING ON
A SINGLE SPECIES OF LORANTHUS. CATOCHRYSOPS PHASMA,
NOT PARSIMON, PROVED TO BEB MYRMECOPHILOUS.—Prof.
Pou.ton exhibited the following eight species bred in 1917-18
by Mr. C. O. Farquharson at Moor Plantation, near Ibadan,
S. Nigeria. Except when otherwise stated both sexes were
present. Mr. G. T. Bethune-Baker had kindly helped in the
determinations, some of which were difficult.
(1) Epamera vasis, Hew.; (2) Epamera sp.; (3) Epamera
laon, Hew., 3 only; (4) Argiolaus alcibiades, Kirb.; (5) A. julus,
Hew., 33 only; (6) A. moesa, Hew.; (7) A. paneperata,
H. H. Druce; (8) Tanuetheira timon, F.
Mr. Farquharson had thus greatly extended the investiga-
tions briefly alluded to in Proc. Ent. Soc., 1917, p. lxi. The
species of Catochrysops of which the pupae were found by
Mr. Farquharson in the subterranean nest of Camponotus
maculatus, F., was not parsimon, F., as stated on the page
referred to above. Mr. Bethune-Baker had examined the
male genitalia and found it to be C. phasma, Butl.
NEW MIMETIC FEMALE FORMS OF CHARAXES ETHALION,
Boisp., AND ETHEOCLES, CR., AND BRED MALE-LIKE FEMALES
OF THE LATTER.—Prof. PouLron exhibited examples of the
following forms :—
Charazes ethalion, Boisd., new 9 forma mimetica swynnertont.
—This is the 9 form d described and figured but not named
by Lord Rothschild and Dr. Karl Jordan in Nov. Zool., vol. vil,
(j-lcexs )
1900, p. 479, pl. xu, fig. 6. It is defined by the “ band and
spots” of the upper surface being * pale blue except the
upper postdiscal spots,” which are generally white as in Q
form a, but sometimes buff as in b, or blue though paler than
the rest of the markings. The admarginal spots of the H.W.
upper surface are dull red above, olive green below (viz.
towards the anal angle). Now that this form is so much
better understood, its mimetic relations clear and genetic
relations partly so, it is convenient that it should be named,
and I propose to dedicate it to the naturalist to whom we
owe nearly the whole of our knowledge on the subject.
Type in Hope Department: one of the females (with white
upper post-discal F.W. spots) which emerged Dec. 13-14,
1917, of the family recorded on p. lxxxi, Chirinda, 8.E.
Rhodesia.
Within the limited area of Chirinda forest in 8.E. Rhodesia
the males of this species of Charares are accompanied by
females of the form rosae, Butl., mimicking the females of
Ch. cithaeron, Feld., one of the dominant larger species in
the forest, by swynnertoni females, mimicking the males of
cithaeron, and by the usual female found wherever ethalion
occurs, 7.e. the 2 f. ethalion which probably mimics another
large species, Ch. brutus, Cr. Inasmuch as rosae has been, in
other localities, accepted as a female form of etheocles the
question arose as to whether the Chirinda forest harboured
this species or ethalion, or a mixture of the two. Dr. Jordan
therefore kindly examined the armature of 4 males and found
all to be ethalion, rendering it highly probable although not
certain that at Chirinda the rosae 2 f. belongs to this species.*
Mr. Swynnerton’s two families bred from known females do
not throw any light on this question, although they prove
that ethalion and swynnertont belong to the same species and
render it nearly certain that the relationship between them
* Since the above paragraph was written, Mr. H. Dollman has
exhibited, Dec. 4, 1918, bred specimens of the manica, Trim., and
phacus, Butl., females, from N. Rhodesia, and has proved that these
forms, both hitherto regarded as etheocles, belong to distinct species.
I believe that the genitalia of the accompanying “males will show that
manica is ethalion and that phaeus is etheocles. If this be confirmed
there can be little doubt that rosae, which resembles manica, is also
a E. B. P., Dee. 28, 1918.
( Txxaa >)
is Mendelian, although which female form is dominant and
which recessive remains unsettled.
The first small family, bred in 1913 from the eggs laid by
the 2 f. ethalion, produced males, 2 swynnertoni females and
1 ethalion 2° of form 6. The second family from the eggs of a
swynnertont female produced 17 males and 14 females of the
same form as the parent. The tendency for the males to
emerge earlier is well shown in the tabular statement :—
Dates of Emergence Males Females
in 1917. (all swynnertont).
Dees Oars means 4 3
APs Hee 74 1
ie a 4 3
eel D— 1S). 2 7
Totals . 17 14
It is much to be hoped that Mr. Swynnerton may be able
to breed from the 2 f. rosae and also succeed in making the
Mendelian relationship perfectly clear—for the first time in a
Charaxes.
Charaxes etheocles, Cr., new Q f. m. rogersi.—Differs from
the 9 f. m. kirki, Butl., in the discal band of the H.W., which
instead of being “ white, slightly bluish proximally, and with
a faint trace of ochraceous at distal edge” (Rothsch. and
Jord., ibid., p. 486), is, in the typical form, orange-ochreous
throughout, thus transforming a mimic of the 3g ansorge?,
Xothsch., into a mimic of saturnus, Butl. This latter resem-
blance is also promoted by the tendency of the F.W. bar
in some individuals to broaden and suffuse the dark ground-
colour with orange-ochreous.
Type, in Hope Department, from Dabida, about 100 miles
W.N.W. of Mombasa, June 22, 1916. A similar form from
Maketao, between Taveta and Voi, July 14, 1910. Four
examples from Dabida_ (1916), and one from Taveta (77 cop.,
Apr. 26, 1905, with a 3 of the f. chanleri, Holl., determined
PROC. ENT. SOC. LOND., I11, IV. 1918. F
( Ixxxai )
by Dr. Jordan), are transitional between rogersi and kirki,
but the development of orange-ochreous is such that the
resemblance to saturnus would probably be strong. Of 2
further examples from Dabida (1916) one is very nearly and
the other fully the 9 f. kirk.
This interesting change in the mimetic likeness as kirki
ranges eastward in the southern part of British East Africa
was recognised by the Rev. K. St. Aubyn Rogers (Trans. Ent.
Soc., 1908, p. 507, footnote), who captured the whole of the
above-mentioned examples (see also Proc. Linn. Soc., 1915-16,
pp. 32-33).
C’. etheocles, new 2 f. m. carpenteri.—Differs from the 9 f. m.
regalis, Rothsch., in the following points: (1) the more
angulated direction and more distal position of the blue band
crossing the H.W., so that it is continuous into the series of
post-discal F.W. spots; (2) the disappearance of the two last
blue discal F.W. patches which form so conspicuous a feature
of regalis; the two last small blue patches of carpenteri
follow the post-discal and not the discal series, of which only
the upper spots in areas 2, 3, 5, 6 are represented; (3) the
discal and upper post-discal F.W. spots are not buffish but
white with an intermixture of blue scales; (4) the greater
size and prominence of the white submarginal spots, and far
smaller development of dull red in the admarginal spots, of
H.W. ‘The red in these spots is restricted to a narrow line
with peacock-blue borders; then follow peacock-blue spots,
becoming olive green at the anal angle.
The wings within the discal spots of F.W. and blue band
of H.W. are faintly iridescent dark blue-black as in regalis.
The effect of the above differences is to produce a mimetic
likeness to the 3 of Ch. etesipe, Godt., of which examples were
taken in the same forest on July 8 and 13, 1915.
Type, in Hope Department, taken by Capt. Carpenter in
the forest near Kakindu, 31° 30’ E., 1° 10’ S. (Proc. Ent.
Soc., 1915, Ixv, Ixxv; 1916, cx), Aug. 3, 1915. Another worn
specimen, taken May 19, 1915, differs in the H.W. blue
band being represented by a series of separate spots, in the
whiteness and greater size of the discal F.W. spots, and in
the greater development of red in the admarginal H.W. spots.
« les )
In the fresh condition this specimen was probably an even
better mimic than the type.
Bred C. etheocles with male-like females from S. Nigeria.—
Hight remarkable females have been bred by Capt. W. A.
Lamborn and Mr. C. O. Farquharson, who first found the
larvae on Adenanthera pavonina (Mimosoid2a) at the Agri-
cultural Department, Moor Plantation, near Ibadan, 8. Nigeria.
The period of pupation is shown in the following table :—
| Larva Found. | Paget aera | rex Ai
| Dec. 2,1913 | Dec. 8 Dec. 16 oI
[Rey erage ooo ke ae Q
seo al Oe ae sn) LO 5 26 é
Sa 5 ae aay , 26 9
Unrecorded oe eal Jan. 1, 1914 Q
As sone i The! 55 3
a Unrecorded | Pra ry 3 |
In addition to these specimens sent to me by Capt. Lamborn,
I have received 3 males and 5 females, bred, except 3 without
records, July 3l—Aug. 6, 1915, by Mr. C. O. Farquharson.
Considering the rarity of male-like females in etheocles it
is astonishing that all these should be male-like. Indeed
Dr. Jordan, after seeing them, suggested the possibility that
they had been affected by the artificial conditions. On the
other hand, the 1913 females were only in confinement as
larvae for a few days, while the size of nearly all the specimens
proves that the conditions were quite healthy. On the whole
I think it probable that the dominant females of this 8. Nigerian
locality are male-like and co-mimics, with the males of Ch.
numenes, Hew., of the males of Ch. tiridates, Cr. I have not
as yet received any captured females from the locality.
No one of these bred females is very like the form alladinis,
Butl., or wirilis, Rothsch., although nearer to the latter.
But among themselves they differ so widely in detail that I
( Ixxxiv )
hesitate to name them, preferring to consider them, at any
rate for the present, as forms of virilis. In most of them
the upper discal F.W. blue spots (whitish in one example)
are distinct in areas 2, 3, 5, and 6, being the most prominent
markings on the wings except the submarginal white spots
of the H.W., the only markings that are not blue in most
specimens. The F.W. post-discal spots can generally be
made out, although very faint. The blue band of the H.W.
is more outwardly placed than in carpenteri, although very
similar in its angulated direction: within it the H.W. as
well as the basal third of the F.W. is a steely blue of great
brilliancy in certain lights in some of the specimens. The
females differ from virilis and many other female forms in
the faint linear development or absence of red in the ad-
marginal spots of the H.W., which are peacock blue (in one
female pale grey), generally becoming olive green at the anal
angle, but sometimes persisting unchanged. The upper sur-
face markings are very elusive and very variable. Although
developed to a much fainter degree they greatly resemble
those of carpenter’, a form which could probably be easily
derived from variable male-like females such as these.
Now that Mr. Swynnerton, Capt. Lamborn, Mr. Farquharson
and the Rey. K. St. Aubyn Rogers (who in 1916 bred the 3
and what is probably the @ form a of ethalion from a known 9
parent of the same form, at Dabida) have shown that it is
not difficult to rear these most interesting of all species of
Charaxes, it is to be hoped that more will be done in breeding
from known female forms in the same and other localities.
It may perhaps be possible to pair in captivity and thoroughly
test the Mendelian relationships.
BUTTERFLIES CAPTURED IN NATAL DURING THE EXTRA-
ORDINARY RAINS OF 1917.—Prof. Povutron exhibited the
specimens referred to in the following letter written by
Mr. C. N. Barker in continuation of his notes in Proc. Ent.
Soc., 1918, p. xxvii. All had been taken in the neighbourhood
of Durban.
“ Mar. 11, 1918. Durban.
‘TIT am sending you herewith a box containing a lot of
this season’s Belenois severina, Cr., which may perhaps interest
( Ixxxv )
you, as showing some effects on butterflies of the abnormally
wet weather experienced out here since the middle of June
last. I am enclosing a monthly record of the rainfall. It
has varied a great deal in localities only a few miles apart,
as you will notice in the printed record for October, which I
enclose. The four Acraea petraea, Boisd., which I took on
the 16th of June, just after a heavy fall of rain, show con-
siderable signs of melanism. The dry-season forms had been
in evidence for some time before the rains fell, and although
there was the usual seasonal modification towards the dry
forms, none of them throughout the winter took on the
extreme dry phases. I went out the following and any
available week-end, but after taking these four petraea found
no more in evidence for a month or two after. In fact, they
only began to come into evidence again in the full wet-season
form at their usual time of appearance. I have been dis-
appointed in not finding any extreme cases of melanism,
but I think this may be due to the unusual coolness of the’
season, due to protracted rains. Moisture must be accom-
panied with heat to produce fullest results.
* The tattered P. lyaeus, Dbl., covered with fungoid growth
I found feebly flying through the bush after heavy and pro-
tracted rains that fell in January 1917. I had a great chase
after it, for the orange growth upon it gave it the appearance
of being some strange exotic species. The Pseudacraea
tarquina, Trim., has been mutilated by some enemy. [|
should infer that it had been seized by one of the large Agama
lizards which are very plentiful about our coast bush. The
pair in coitu may also interest you.”
The last-mentioned pair was a dry-season $ i cop. with a
wet-season 2 of Byblia goetzius, Herbst., taken Oct. 16, 1916.
The farquinia was an excellent example of symmetrical injury
to the hind-wings. The orange powder plentifully covering
the under surface of the hind-wings of lyaeus was found to
be pollen by Dr. A. B. Rendle, F.R.S. The quantity was
very remarkable, and nothing like it had been seen by any
of the African naturalists to whom the specimen had been
shown. Dr. Eltringham had compared the petraea with the
Hope series from Natal, but considered that they did not
( Ixxxyi- *)
differ from the average of other years. Dr. Dixey had
written the following note on the Pierinae :—
Pierinae captured at Durban, Natal, by C. N. Barker.
The dates of the captures are from July 7 to Dec. 2, 1917.
Mr. Barker notes that the season was abnormally wet after
mid-June.
The species are Belenois gidica, Godt., and Belenois severina,
Cram.
B. gidica.—One specimen, Sept. 2; two specimens, Nov. 18
and Nov. 30 respectively. An early September example would
generally be dry; this one is wet, though with a trace of the
dry-season character about it. The November specimens are
wet, as would be expected in ordinary seasons.
B. severina.—Four caught in July, two in August, one in
September, five in November, one in December.
The July and August examples are of the full dry-season
form, as they would be in ordinary seasons. The November
and December examples have the wet-season ground-colour
and the dry-season veining; this is a usual condition at this
time of year in ordinary seasons. <A similar condition was
produced in 1905 by Dr. G. A. K. Marshall at Salisbury,
Mashonaland, by exposing a brood of B. severina, which
would normally have emerged as the dry-season phase, to
artificial conditions of moisture throughout the larval and
pupal stages (see Proc. Ent. Soc. Lond., 1907, p. xin).
On the whole, the abnormal character of the season appears
to have had little or no influence on these Pierines.
Ex-GERMAN East AFRICAN BUTTERFLIES AND THEIR
RELATION TO THE SEASONS.—Prof. PoULTON said that he had
received the following information, supplementing that com-
municated to the meeting of May Ist last (p. lvi), from
the Rev. K. St. Aubyn Rogers at Kongwa :—
* Feb. 28, 1918.
‘The wet season this year has been much less heavy than
last year, and the * break’ has been much more pronounced.
We had heavy rain in January (about 83 in.) and the first
Gelizxzvnt >)
week in February, but the ‘last three weeks have been dry
and sunny and rather windy.
~ Iam sending you. the little Alaena which occurs here,
It is not uncommon, but very local, and I have only found
it in the forest on the hills behind the house, which is com-
pletely deciduous in the dry season. I make a guess that
it is A. reticulata, Butl. [It is A. johanna, KE. M. Sharpe. |
I am also sending a specimen of the Belenois, which cannot,
I think, be separated from B. picta, Neave. [Dr. Dixey
agrees with this opinion.] It is extremely variable here, and
some specimens are much more like Neave’s figure, and
others much less like it.
“I took about eight males of the form of Acraea acrita
I sent you in my last letter lacrita ambigua, Trim.: Proe.
Ent. Soc., 1918, p. lix, n.], and this week I have two females.
“ Mar. 7, 1918.
[have not vet seen Dr. Dixey’s paper in which he described
Teracolus rogersi, so 1 cannot be certain, but I believe I have
specimens from these parts. It does not occur on the low
eround, but well up on the hills, and is by no means common.
[Dr. Dixey has found three 3 examples of rogersi in Capt.
Carpenter’s collection from St. Michael’s; see p. cli] I am
quite convinced that my specimens do not belong to any of
the common orange-tipped species of Teracolus. Last Saturday
I got another orange-tipped Leracolus, which puzzles me.
On the upperside it looks like an extreme dry 2 of T. phlegyas,
Butl., but the underside does not agree at all with the dry
forms of this species I took last year. I captured a similar
specimen on my way to Mamboya in February last year, but
as it was much shattered, and I took it for a © TI. phlegyas,
I did not keep it.
“ Though we have had a month’s fine weather now all
Leracolus and Precis are still @, and we expect more rain
any day. There have been some thunderstorms about lately,
but we have not had any here.
* Tenclose a small Lycaenid which I think must be Aloeides
takosama, Wallern. It is common here locally in the rains,
and varies a great deal.” A long series of the same form,
( sboxxvin? )
taken in the rains by Capt. Carpenter at Itigi, between
Mar. 21 and Apr. 6, 1917, showed such marked variation
that it seemed doubtful whether takosama was not the same
species as Cramer’s prerus. Structural investigations were
required.
** Mar. 21, 1918.
“The rains have been very deficient this year except
during January, and the crops will be very poor; in fact,
unless rain comes soon there will be famine in some districts.”
Carr. G. D. H. CARPENTER’S FuRTHER Notes on EX-GERMAN
Kast AFRICA, ALMOST EXCLUSIVELY East oF Laks
TANGANYIKA.
Owing to the loss of letters from Capt. Carpenter between
July 16 and Oct. 5, 1916, there is some inaccuracy in the
account published in Proc. Ent. Soc., 1916, p. exxvin. On
July 16 he was at Namirembe Bay at the S.W. corner of
Lake Victoria. In the first half of August he was at 32° 20’ E.,
3° 20’ §., in a temporary camp in flat, dry country with
thin, deciduous bush, arriving about the 18th at 32° 45’ E.,
3° 45’ §., in the neighbourhood of St. Michael’s Mission, in
country of similar type with granite outcrops. This was the
“place of rocks”? (¢bid., exxvili), where he remained until
about the middle of October, reaching Muanza, the well-
known port on the 8. coast of Lake Victoria about Oct. 20.
The following extracts, arranged regardless of date in what
seemed the most convenient order, give some of the information
recorded in the missing letters.
** Mar. 6, 1917.
‘I gather from your saying that you didn’t understand
the allusion to ‘the place of rocks’ that a long and, if I
may say so, an interesting letter * of mine has got lost—very
probably it went down in the ‘ Persia,’ which contained a
large EK. African mail. It described a camp at St. Michael's
about half-way between Muanza and Tabora, among piled-up
eranite boulders which sheltered countless Hyrax (the first
* After reading Proc. Ent. Soc., 1916, p. cxxviii, Capt. Carpenter
wrote on May 20, 1917: ‘* At least two letters written between July 16
and Oct. 8, 1916, never reached you.”
(--Ixxxix |)
time I had met them) and Caracal cats (or rather Lynxes, I
suppose) and interesting birds and lizards and things. I
cannot now remember what I said, but it was probably
written early in September or end of August, [ think.
“ Oct. 6, 1917.
*“ No, I fear I can’t re-write the missing letters about
St. Michael’s: the enthusiasm of the time is gone!
** Aug. 9, 1917.
“What's coming may interest you. It got lost in a
previous letter that didn’t reach you. Firstly, about a
Jumping Shrew (Macroscelid?), which I found, dead, on
safari, about this time last year. I asked my boy the native
name for it, for apparently they know it quite well and
differentiate it from Rodents. In Kiswahili it is called
Kasanji (or Kasangi): my own boy said it was crepuscular
rather than nocturnal. A Muganda called it Musonso, and
said it lives in very long burrows underground and ate white
ants, but also said it ate the same as rats and mice (so there
is probably confusion here). Both boys said this—that these
(apparently feeble) animals entice mice to come to them by
squealing, and then kill them, but do not eat them. My
Swahili boy also said that two or three will collaborate in
attacking a snake, or lie in ambush for it, and kill it—probably
mere folk-lore !!
** Nov. 30, 1917.
“It was on July 5, 1916, at Namirembe Bay that I saw
the first “Jumping Shrew.’ I saw three large ones here
fat Lulanguru, 17 miles W. of Tabora| one evening, quite
close. They did not actually jump, but their quick gait
was much like that of a rabbit when it moves from one spot
to another with powerful thrusts of the hind-legs. I was
near enough to see how the absurd tubular noses were con-
stantly wrinkled up. They sat on the ground with the tail
straight out behind them.”
Dr. Oldfield Thomas, F.R.S., to whom the description has
been submitted, considers that the “* Jumping Shrew’ is no
( xe )
doubt a member of the Macroscelididae and most probably
an Elephantulus, but the genera are very closely allied,
* Aug. 9, 1917.
“ Now about ants. I was talking about Megaponera to a
C.M.S. missionary from Toro, and he said in that part of
Uganda they are well known for their Termitivorous (!)
habits. But he added this curious tale. There is another,
‘small, red,’ ant which the natives call * Nabi,’ and they say
it comes into a house and eats all the Termites, but doesn’t
go away until it has * sown is mushrooms.’ I asked the
missionary what he meant by that, and he said that the
departure of this ant is followed by a crop of tiny fungi in
the Termite runs. I can only explain it by some fungus
which the Termites keep under restraint, flourishing rampantly
in their absence. For the natives did not say that the * Nabi’
comes back to eat its mushrooms ! ! ”
Having thus, as far as possible, filled up the gap in the
series of letters published in Proc. Ent. Soc., 1916, the corre-
spondence is continued in order of date—with here and there
a passage inserted, for the sake of convenience, out of its
chronological position. The last letter published in 1916
(p. exxviii) is dated Oct. 5 of that year; the present series
begins only a month later.
These letters, like the earlier ones, include many observa-
tions and descriptions that are not Entomological, but throw
light on the interesting and little-known country in which
the Entomological work was done and the unique conditions
which now prevail.
Many of Capt. Carpenter’s observations on mimicry are on
the lines of Dr. Marshall’s work published in our Transactions
for 1902, but the species are nearly always different, and in
such a difficult and controversial subject the independent
testimony of another observer, who from the force of cir-
cumstance was unable to study the work of his predecessors,
is of great value. Furthermore Capt. Carpenter has done far
more than confirm; he has added new conclusions of much
interest.
In the variety of inquiries involved in the study of Capt.
(-xa_7)
Carpenter’s letters and material I have received kind help
from the following friends :—Mr. H. E. Andrewes, Mr. G. J.
Arrow, Mr. G. T. Bethune-Baker, Mr. K. G. Blair, Dr. G. A.
Boulenger, F.R.S., Mr. G. E. Bryant, Dr. F. A. Dixey, F.R.S.,
Mr. J. H. Durrant, Dr. H. Eltringham, Dr. C. J. Gahan,
Sir George Hampson, Dr. G. A. K. Marshall, the Rev. F. D.
Morice, Mr. 8. A. Neave, Lord Rothschild, F.R.S., Dr. Oldfield
Thomas, F.R.S., and Mr. Rowland E. Turner.
“ Nov. 3, 1916. Ndala (33° 15’ E., 4°45’ S.).
* By this time you should have received a box of interesting
specimens collected in the country between our start-off point
at the N.W. tip of ex-G.E.A. and the 8.W. corner of the lake.
‘ T forget when I last wrote, but since then my connection
with the Belgian troops has come to an end, as when they
had got to Tabora all the Uganda porters who had been
loaned, to get them there, were recalled, and we all reached
Muanza at the end of October. Muanza is as different from
Entebbe as it can be. It is a place of granite rock which
crops up everywhere, forming islets in the sound at the mouth
of which Muanza lies, and hills of small size ashore. These
are all grown with bushes, now bright green, and it all looks
very pretty, but absolutely different from Entebbe with its
forest growth, papyrus swamps, banana plantations, and
flat-topped hills. Rice and millet are the crops at Muanza.
I was only there two days, as I was ordered off at once to
my present post along the Lines of Communication between
Muanza and Tabora (200 miles out, which I did in a car in
two days: it would otherwise have been a fortnight’s safari).
It is only 40 miles from Tabora, which I hope to see some
day. There is very little to do here, and I have a much
bigger staff to help me to do it than I ever had when we
were on the march. It’s rotten country, very very flat
(extremely hot and,dry, though all the trees are brilliant
with young green, possibly because water is very near the
surface), and with thin bush, and a great part of it has been
cultivated at one time or another, so that it’s pretty hopeless
for butterflies. When I have read my last batch of papers
and finished my Xmas letters I shall have very little to do
(xem)
except think about the treasures I have caught, and wonder
when I shall have a chance of working them up. At one
time I thought I might be coming home this winter, but they
are not letting any doctor men home on leave.
“ T hope I shan’t be kept here long. I am now nowhere
near any kind of ‘front.’ All the future fighting will be in
the S.E. part of the country, south of the railway, which is
now entirely in the hands of the allies and being used by us.
* Dec. 14, 1916. Ndala.
“ Yes, I had thought that the smaller yellow, orange-tipped
Pierine |Teracolus incretus, Butl.| might be associated with
Eronia leda, Boisd.
“| went about 150 miles along the ‘ Central Railway’ to
a case of Blackwater Fever, about a week ago and have only
just got back. I was glad to see the railway (which is,
naturally, of great use to us now). It seems to have been
built * regardless,’ and everything is most solid and expensive.
Every little station (about 10 miles apart) has a stone and
concrete building. But what the stations are for no one can
tell: they are just islands in the midst of most hopeless
thick bush—mile after mile of it—and it’s the most extra-
ordinary contrast between a journey on this line and one on
the Uganda Railway. There ave giraffe and a few big antelope
and lions, but I saw none of them. The bush can’t even
produce butterflies! I am sending to Wiggins a small box
of sundry insects and asking him to forward it to you. I
hope the few butterflies may be of interest: perhaps the
skipper that frequents ant-bear holes may be so, also a
Liptenine [Zeriomima pallida, Trim.| which looked like a 3
Lymantrid (e.g. ‘ Vapourer’) on the wing.” The species of
Sarangesa mentioned in Proc. Ent. Soc., 1916, pp. exxix,
cxxx, were included in this box. Two S. pertusa, Mab.,
and 4 S. synestalmenus, Karsch, were labelled ‘‘ In ant-bear
hole; noon, July 23, 1916,” at Namirembe Bay, S.W. Victoria
Nyanza, and 1 synestalmenus ‘‘In ant-bear hole, noon,
32720" 32 207 (S22 Capt. Carpenter was in a temporary
camp at this locality and the date was Aug. 8-14, 1916. A
little earlier on Aug. 1, at 32° E., 3°S., he found a male of
(@ Xciinan)
the remarkable Liptenine Hpitols miranda, Staud., floating
dead and headless on a forest pool—a noteworthy extension
of the range of this species.
* Jan. 3, 1917. Ndala.
* You will see that I have hitherto had no chance of reply-
ing to the late Colonel Manders’ remarks on my Pseudacraeas
in Proc. Ent. Soc., 1915, p. xxii, so I am writing something
here.
* Firstly—the bird question. I certainly do not agree that
‘the bird population on the mainland and on Bugalla is
practically the same.’ One striking exception ‘at once leaps
to my mind:—the extraordinarily greater abundance of
Flycatchers, of two types, on Bugalla. The most noticeable
of the two is the one I called * Kunguvu’ in my Report on
Glossina. I think it must be a Terpsiphone [considered by
the authorities of the Natural History Museum to be Tf.
cristata, Gmel.|. It is red-brown with blue-black head, and
the cock has very long floating white tail plumes. This is
immensely more abundant on the islands than at Entebbe
on the mainland, and its ringing call was the first bird note
in the forests at daybreak, so that I soon got very familiar
with it. When, in 1914, I visited other islands, I noted
that the call varied in pitch very slightly from that of the
Bugalla birds, and thus one is almost forced to conclude
that some islands have their own race of this bird, and that
they do not cross from mainland to islands. They are
retiring birds, are not seen in the open, and have the typical
Flycatcher habits. .
“The other of the two is a black and white species
| Platystira jacksoni, Sharpe, according to the Natural History
Museum and Mr. 8. A. Neave| with red fleshy protuberance
over the eye. Its call, totally different from the other's, I
also have deeply rooted in my memory, and learnt to whistle
it and make the bird answer. I think this bird also was more
abundant on the islands than at Entebbe. In 1914 I noticed
that the call of the birds on the group of islands I was then
working on was different in pitch—though really the same
call—from that of the Bugalla birds.
(-xervey
“ Again—one striking feature—I never saw a Drongo on
the islands. I should think they must live on the mainland
round Entebbe, but have not seen one, though I have not
done any work on the mainland. [Mr. Neave does not
remember whether he saw Drongos at Entebbe, but thinks
the locality unlikely for the common species. |
“ As regards the passage to and fro of birds from mainland
to islands, Col. Manders appears to think that such a passage
must be an objection to my explanation. But why should
it be? A bird passing across 25 miles or so of water carries
with it the memories of its last hunting-ground, surely ?
I know that ‘Bee-eaters fly over wide stretches of water, as
I have seen them when canoeing.
“Now Col. Manders thinks my table in the Sleeping
Sickness Reports shows that birds do not eat butterflies.
Surely this is hardly justifiable. Firstly, I was not searching
for evidence as to what birds eat, but only as to whether
they ate Glossina; 1. e. I was looking for one specific object-—
the tsetse fly's wings: so any piece of a butterfly that was
not grossly obvious would have been likely to be passed
over; for I used only a low-power dissecting microscope and
not one high enough to distinguish Lepidopterous scales,
which, as Swynnerton has shown so admirably, is absolutely
necessary. One could deduce equally well from my table
that birds do not eat Diptera !
“Col. Manders makes some large assumptions. On the
evidence of 116 birds he says ‘we may assume that none
|7. e. no tasting experiments| took place.’
‘He talks about ‘ aposematic crimson and blue bodies of
Dragonflies.” On what evidence does he call them * apose-
matic’? Surely a sine qua non of an aposematic insect is
a method of display by slow gait, feeble flight, sluggishness,
etc. Are any of these characteristics of Dragonflies? There
is, one would think, much more ground for ascribing these
colours to sexual selection (if this hypothesis holds good at
all), seeing that the males are often so much more gaudy
than the females.
“Lastly, a propos of his quotation from Fabre, was not
that great observer's objection to the mimetic explanation of
( xev )
the colours of Volucella inanis, L., due to the supposition—-
in those days, before its habits were fully known—that its
appearance protected it from the wrath of the wasps in whose
nests if was supposed to be parasitic? I understand that
now it is known to be beneficial in the nest rather than other-
wise, the larva feeding on débris. But surely the modern
view is not that Volucella needs to be protected against the
wasp, but against birds that fear the wasp. [See Trans. Ent.
Soc. Lond., 1904, pp. 661-665. |
* T had the rottenest, dullest Xmas I’ve ever had. There
was nothing to read of any kind. I have said before what a
rotten place this is for butterflies, and no Xmas fare, indeed
even rations very poor. We have now no jam, sugar, lamp-
oil (but candles for the present), or soap issuable! No vege-
tables for weeks! However, one can get eggs and mangoes
abundantly, and milk, and I have some porridge and syrup
which helps out. It’s funny what one can live on day after
day the same. Breakfast is the best meal—porridge with
syrup and milk, bacon and eggs, bread and jam (just finishing
now). Bread, soup, meat and mangoes form other meals.
Luckily I have had some butter, which helps, but it is nearly
finished now !
“We are very isolated—three days from Tabora (where
one cannot get anything) and three weeks from Muanza.
An occasional motor-car, which usually breaks down en route
to Muanza, brings up the belated mails. A parcel of * goodies ’
which my mother sent for mid-October in August is. still
trying to get to me! Well, that’s another long grouse !
“ Jan. 14,1917. Ndala.
“Tam taking the opportunity of a friend going back to
Muanza and Entebbe (from here—Ndala, where I still am—
33° 15’ EH. and 4° 45’ 8.) to give him a box of ‘ dudus’ for
Wiggins to post for me at Entebbe. You may label them
Ndala (for it appears on the map, being a Mission Station),
with latitude and longitude as above. A few I got recently
on a very enjoyable safari (except for G. morsitans !) in the
neighbourhood. It was quite a joy ride, and I had no respon-
( xcevi )
sibilities. It was nice to be able to go as one pleased with
just one’s own kit. We had (I went with the Political Officer)
very fine sunny weather, but now the rains have just begun,
and go on until about June or end of May. They say that
now it means we can’t finish off the boches (who are around
Mahenge) until August, as the country is impossible in the
rains down there.
* Well, now, I will look through my journal for notes on
any of the insects I send—they are not all butterflies; some
are Asilids with prey.
“To begin with—a Millipede, a giant black species about
6 inches long, I should think, brown-legged, really very
handsome. On Dec. 26, before breakfast, I saw one walking
along, and I picked it up. Millipedes when picked up coil
up in a ring and ‘he low,’ but this didn’t. He was of an
original temperament, for he wriggled violently, and when I
dropped him, lay on his back and writhed in such a serpentine
manner—actually making progress thus—that it was quite
terrifying! Subsequently, as he walked along, I irritated
him with my stick, and he turned over on his back and writhed
again in serpentine manner. I doubt if any native who was
not familiar with these common creatures would have gone
near it. I was much interested because I have seen and
handled a great many of these handsome armour-clads (they
were very abundant on the islands, though I think this was
the biggest I have seen), and since then have tried to make
others of the same size and appearance perform in the same
manner on three occasions, but I have never met with another
performer. Perchance, in half-light, it might save one from
being eaten. Some animal does eat them, I fancy perhaps
jackal or mongoose, for one finds their rings in old dried-up
droppings.”
[Capt. Carpenter wrote in a letter of June 20, 1917: “ Re
the Millipede—I fancy it writhed on its back because the
movements were so lusty that the delicate legs might have
interfered with the freedom of the movement or even been
damaged by it. I tried several others of the same species
afterwards, but never got another individual to writhe in
the same serpentine manner.” |
(-*xevii- )
“On Dec. 28th I got a beautiful Mutilloid spider. I was
collecting on a road through the bush and picked up several
Mutillids. But one turned out on closer investigation to be
the spider which I send in a tube with the Mutilla it resembles,
taken at same time and place. It used its fore-legs to mimic
the antennae of the Mutilla, just as does a spider mimicking
an ant. Its manner of movement was altogether Mutilloid,
and its colours exactly (during life) matched the dull red and
black of the Mutilla. 1 wonder if Mutilloid spiders have
been described before ? ”
The specimens in the tube are accompanied by a corre-
sponding note which also states that the ~ colours exactly
matched.” The Mutilla appears to be the same as a 2 taken,
Dec. 1903, in cop. with a very different 3, by Dr. Marshall at
Bulawayo, and named by the late Col. Bingham M. charaxrus,
Sm. Mr. A. W. Pic'ard-Cambridge considers that the
spider belongs to Prosthesima (Drassidae) or a closely allied
genus, and that the species is near P. albomaculata, O. Pick.-
Camb., taken by Dr. Marshall as a Mutilloid mimic, at Salis-
bury, Mashonaland (1898-99). See Trans. Ent. Soc., 1902,
p- 511; Proc. Zool. Soc., 1901, p. 11, pl. v, figs. 2-2c.
Capt. Carpenter took the same species of spider later at
Lulanguru (see p. cxxxv). At this locality and at Ndala: he
also observed and captured several examples of black, white-
marked Carabidae together with their Cicindelid mimics.
All the species are different from those observed and figured
by Dr. Marshall in Trans. Ent. Soc., 1902, pp. 511-515, and
pl. xvii, and some of them appear to be undescribed. Capt.
‘arpenter did not comment upon the general Mutilloid effect
of the black-and-white pattern during rapid movement.
Dr. Marshall (bid., pp. 511, 512) points out that it is this
part of the Mutillid pattern and not the red thorax which
attracts attention in life.
Capt. Carpenter's captures of members of this association
are as follows. On Dec. 18, 1916, at Ndala, the Mutilloid
Carabid Piezia sp. was, together with its Cicindelid mimic
Dromica (Myrmecoptera) erikssoni, Horn, “Taken on a road,
almost in the same spot.” The mimic bears the note “ This
does not fly as readily as, many Cicindelids.” Then, at the
PROC. ENT. SOC. LOND., III, Iv. 1918. G
( xevit)
same place, on Dec. 20, and again on Dec. 21, another
Mutilloid Carabid Polyhiima sp. was captured with its mimic
Dromica (Myrmecoptera) newmanni, Kollar. The pair of Dec. 21
bear the note “ Taken on same stretch of road.” About a
year later, on Nov. 20, 1917, at Lulanguru, a large species
of Polyhirma, and in this case with the black-and-white
Mutilloid pattern more sharply and clearly expressed in spite
of its disproportionate size, was taken with its mimic Dromica
purpurea, Bates, and two examples of Dromica sp., the mimic
of a smaller Mutilloid Polyhiima taken the day before. The
mimetic associations between the beetles are suggested on
the accompanying labels, including the probably synapo-
sematic relationship between the two Carabid models. In
all. these Polyhirmas, except the largest species, the
Mutilloid black and white is dully expressed, as also in
the mimics, while in the mimic of the largest species it is
evanescent.
The- splendid Mutilloid mimic, the Carabid, Hecoptoptera
cupricollis, Chd., which caused Dr. Marshall “to hesitate
more than once before venturing to handle it” (cbid., p. 512,
pl. xvu, fig. 11), also deceived Capt. Carpenter, for his note
on a specimen of Dec. 8, 1915, on the bank of the Kagera
River, near Nearama, about 37 miles W. of the Victoria
Nyanza, is: “ Mutillo.d! Quite tock me in,” and again
“very Mutilloid” on a Ndala specimen of Dec. 16, 1916.
The female of Dolichomutilla guineesis, F., a very perfect
model, except that its thorax is black instead of the reddish
colour so common in Mudtillidae, was taken at Ndala a few
weeks before, on Nov. 13.
“ About at the beginning of December we had a burst of
rain which left large puddles on the dry roads. Almost ~
immediately after one saw Crabs running about! It seemed
strange to see them away from any large body of water,
though there are permanent water-holes. A large puddle
which I had noticed to have been frequented by crabs on
Dec. 15th—at which time it had been just formed—was, on
Jan. 5rd, reduced to a mere cupful of water, in which I found
a young crab, very minute. Its metamorphosis cannot take
very long. for on Dec. 2nd the puddle had not been formed.
( “xerx: )
It was probably formed about the 10th. This residue of the
puddle was a wriggling mass of tadpoles and small fish !
How did the eggs get there?!”
[Dr. G. A. Boulenger, F.R.S., kindly writes: “I have
often heard before of water-holes in Africa being filled after
months of drought and then at once alive with fish, which
must have been aestivating in the ground, probably at a
considerable depth, where there was just enough moisture to
keep them alive. The tadpoles are easily accounted for, as
frogs breed at once after rain, their eggs hatch in a couple
of days, and the success of their brood depends only on how
long water, or at least moisture, will remain to allow the
young to complete their metamorphosis. ” |
* On Dec. 30th I got two Asilids with prey, one a winged
3 black ant, the other a typically aposematic black and
scarlet Hemipteron (1 think a Reduviid). It was alive and
unfortunately escaped. That it was not dead seems to be
another instance of the well-known hardihood and retention
of life of aposematic imsects in general. I feel sure Asilids
must 7ject some poison into their prey when they first thrust
the proboscis in, for I have watched one catch an insect and
immediately caught them both and found the prey (even a
vigorous insect, a Cicindelid, for instance) as collapsed as if
it had been stung by a Fossor. [Kirby and Spence (5th ed.,
1828, vol. 1, p. 274) speak of the instantaneous death of the
prey: the injection of poison is suggested in Trans. Ent.
Soc., 19C6, p. 365, footnote.| On this same date I got a
small black and yellow predatory wasp [the Fossor (Sphegidae)
Palarus latifrons, Kohl, allied to Astata and Crabio| carrying
a stung honey-bee [Apis mellifica, L., var. adansoni, Latr.|—
heavier than itself. I send both.”
The observations on Ammophila beninensis, Pal. de Beauv.
(lugubris, Gerst., see p. cxxxvi), made on Jan. 3, are published
in Proc. Ent. Soc., 1917, p. xli.
“On Jan. 4th I saw, about 7.30 a.m., large numbers of
winged Termites belonging to a very minute species | Hutermes
sp.] emerging from holes in the ground, on a cleared track. As
fast as they came out they huddled together, each one’s head
beneath the folded wings of the one in front, so that all one
(scr)
saw was a mass of wings, those of each Termite overlapping
another's, so that the appearance reminded one of a piece of
butterfly’s wing seen under a microscope. They made no
attempt to fly away. After a while the mass began to elongate
in two directions, and two long lines, headed by workers and
soldiers, began to move away. But the Termites very soon
stopped and bunched together again. What a meal for a
Wagtail had there been one there. This species of Termite
comes to light in the evening in a very annoying way. I
send you some of them.
“On Jan. 5th I found under bark of a dead tree a small
Carabid |Thyreopterus flavosignatus, Dej.| and several large
Erotylids | Mimodacne grandipennis, Fairm.|, both species of
the same colour scheme—black, with two orange transverse
bars. By a very curious coincidence, only the night before
some insectivorous animal had been in my hut, and left a
dropping behind it in which I found an elytron of this
Erotylid, and wondered what beetle it was, as I had not
hitherto met with it. The Carabid is a small one, and the
other so very much larger that it is difficult to believe that
mimicry is at the bottom of the resemblance (unless the
Erotylid is distasteful and the Carabid a synaposeme).
“On Jan. 9th I caught a very remarkable-looking large
black fly with conspicuous red head. I caught it on the
wing—it flew very slowly—and settled conspicuously on a
leaf. I send it you—I cannot place it at all.”
The fly is Bromophila caffra, Macq., figured as one of a
Rhodesian group of insects in Trans. Ent. Soc., 1902, pl. xxii,
fig. 27. Dr. Marshall speaks, on p. 531, of its abundance
and sluggishness, and states that “it ejects a yellow liquid
from the mouth when handled, and was refused when offered
to my baboons and Cercopithecus monkey.”
“On Jan. 7th I got a very fine large black Carabid [Anthia
fornasinn, Bert.| with dull white margin to elytra, running
over bare ground in moonlight. As it 1s a common type of
colouring I picked it up to see if 1t was the most common
species, and saw it was one I had not yet seen: I send it
to you. I was looking at it by full moonlight, holding it
about 18 inches away from my face. The fluid which it
(y cly.")
ejected hit my left eyebrow and caused immediately a very
severe burning sensation, and though I at once bathed the
place in water, the burning sensation did not fully pass off
for half an hour. [The defensive secretion of the Anthias
is also treated of in Dr. Marshall’s memoir: see especially
pp. 510, 511.] I may here say that my monkey, wher I
put down one of the commonest of this type of beetle, showed
every sign of fear and actually ran away from it.
“On Jan. 10 a number of handsome black-and-white bees
| Anthophora nubica, Lep.| were seen apparently roosting for
the night all together on bare twigs of a large Tamarind
tree. I send you a few. I had not met them before. On
the same day I first saw the large and curious Lycids, some
of which I send |[Lycus (Chlamydolycus) sp. nr. trabeatus,
Gueér.; the same as species 5 taken at Itigi, Proc. Ent. Soc.
1917, p. lvin]. The male has enormously expanded elytra.
(My monkey won't have anything to do with Lycids! This
will appear later when I send you my account of * Taste
Experiments.)
“T think that’s all for the present. I am going off to-
morrow—perhaps to be permanently there—to Igalula, the
nearest station on the railway—about 40 miles E. of Tabora,
where there is a recruiting depot for King’s African Rifles
and porters. I have to examine recruits, but whether I am
coming back to Ndala I know not. Iam taking the monkey
with me, so hope to carry on. I have got records for nearly
100 species now.
* Jan. 18, 1917. Lgalula.
* T arrived at Igalula to-day, but as there is not here the
recruiting depot which I understood was, I shall presumably
have to move further down the line to Itigi—about 150
miles EK. of Tabora.”
Capt. Carpenter’s observations on a Bembex attacking
Hesperid butterflies (Proc. Ent. Soc., 1917, p. xli) were
included in this letter. Other specimens also captured on
the journey, Jan. 17, from Ndala to Igalula are referred to
in the following letter.
(- ci)
“ Mar. 12, 1917. Itigi (34°.30’ E., 5° 45’S.),
4278 ft., on the Central Railway, about 150
miles E. of Tabora.
“On Jan. 17th I got a fine large Pierine [ Teracolus ducissa,
Dogn., S| new to me, the Belenoid Hesperid mentioned
before, a fine rosy Acraea [A. acrita ambigua, Trim., 3], only
once, I think, caught hitherto, and some other Hesperids
new to me.” One of these, Oxypalpus harona, Westw., is
mentioned in the extract quoted in Proc. Ent. Soc., 1917.
p. xl, together with the ‘ Belenoid Hesperid,” Lewcochitonea
hinder, H. H. Druce. The following interesting note on this
latter species accompanied the specimens :—
“Jan. 18, 1917. Black and white Hesperid.—The first I
saw, on road through * Xerophilous forest,’ sitting on patch of
wet mud with wings outspread. I thought it was a Belenois
new to me, until I got within striking distance and saw its
short antennae out in front of it. (N.B.—I at first thought
it rather a curious attitude for a Pierine!!) Subsequently
caught others, most with wings closed in Pierine attitude.
One was closely associated with the two Belenois |B. gidica,
Godt., g, and B. severina, Cr., 3] sent with it. I watched
them several times. The Hesperid would settle and the
Pieries come and settle as close as possible to it: some
Catopsilia also—a pale green species like a 2 Brimstone
[evidently C. florella, F., 3]. I failed to catch all three at
one stroke of the net, but caught Hesperid and one, and the
other (the identical one which had been drinking with the
Hesperid) a few minutes later. When the net is put down
over them the Hesperid does not at once fly up with the
Pierines, but remains calmly sitting. Curiously enough, the
first one I saw was the only one that had wings outspread.
Its flight is not so dashing and irregular as most Hesperids :
indeed one might say (but I won't, for fear it’s only imagina-
tion!) that its typical Hesperid flight has become Pierine !
But I don’t think the flight is sufficiently Pierme to cause
the butterfly to be mistaken for a Pierine on the wing: there
is still a certain Hesperid touch about it.”
The resemblance of the allied white, black-marked Hesperid,
Abantis levubu, Wallgr., to the commonest Pierines at Taveta,
( ci)
was pointed out by the Rev. K. St. Aubyn Rogers in Trans.
Ent. Soc., 1908, p. 540. The following specimens captured
at Taveta, on May 10, 1905, by Mr. Rogers are in the bionomic
series of the Hope Department :—B. severina, 2; Teracolus
halimede, Klug, 2; T. celimene, Lucas, 9, and A. levubu, 3.
Mr. Rogers considers that at Taveta B. mesentina forms,
with severina, a centre for the convergence of other Pierines,
and he writes of the above list, to which mesentina might be
added, ‘‘ all these species bear a considerable resemblance on
the wing, and all settle in exactly the same way with wings
half raised. I think Teracolus castalis, Staud., might be
added to the assemblage. ... The Hesperid is of great
interest, as mimicry in this group is so rare. The species
has a rapid flight as is usual in this family, but its compara-
tively large size and its conspicuous black-and-white colouring
mark it out at once from its congeners and give it a strong
superficial resemblance to the forms mentioned above ”
(ibid., p. 540).
The specimens captured at mud on Jan. 18, 1917, may be
compared with 18 male Pierines settled on a patch of cowdung
and all under the net together, on Aug. 25 at Itigi in the
dry season (from about May 25):—8 Belenois mesentina, Cr.,
5 B. severina, Cr., 2 Pinacopteryx simana, Hopfi., 1 Teracolus
eris, Klug, 1 Herpaenia eriphia, Godt., 1 Glutophrissa
epaphia, Cr.
feturning to the letter of March 12 :—
“On Jan. 29 I got. two Lycaenids new to me, IJ think
|Epamera aphnieodes, Trim., and Argiolaus silarus, H. H.
Druce]. Also on Feb. 5, one do. do. [Castalius hintza, Trim.].
* Pinacopteryx simana is very abundant at Itigi [see Dr.
F, A. Dixey in Trans. Ent. Soc., 1918, p. 191]. By the way,
the Mud-drinker’s aposeme is scarce hereabouts, and I think
there are only Mylothris agathina, Cr. (commonest), and one
Phrissura. [In relation to this subject Capt. Carpenter wrote
on Nov. 2, 1917, of the Lycaenid Phylaria cyara, Hew., “I
have never seen it except drinking at mud.” See Proc. Ent
Soc., 1915, pp. Ixvi, Ixxi, Ixxvitxxix.] Belenois is not
common: indeed Teracoli are the most abundant; but even
now Itigi is a poor place for butterflies.
( civ )
*“ Feb. 26, 1917. Itigt.
“ Things drag on here and we are all very sick of the
business. But there seems no chance of rounding up the
Huns that remain until the rains are well over and the
marshes have dried up a bit. So for several more months
I suppose I shall continue to vaccinate porters, and treat
those that are sick, etc., etc. So do we win the war!
“ Mar. 6, 1917. Itigi.
“IT was much interested in your phrase that ‘the African
vegetation anticipates the wet season.” Though I had noticed
the facts the full meaning had not come to me, and the word
‘anticipates > brings it home.
* Mar. 24, 1917. - Itigt.”
This letter contained the account of the 272 Lycid beetles
caught on one plant, Mar. 23 (Proc. Ent. Soc., 1917, p. lvu),
also the following note: “I caught my first A. zetes acara
for many months, here, to-day. It was a very EK. specimen
as one would expect.” An undated letter, written a little
later, refers to the same species as follows: ‘* By the way,
I have at last caught a couple of zetes acara here, and both
were, as would be expected, the most Eastern I have seen.
But it is extraordinarily scarce.” Of the powerful combina-
tion of large red-and-black Eastern Acraeas Capt. Carpenter
caught in 1917, zeles acara, Hew., pseudolycia astrigera, Butl..
and anemosa, Hew. They are very much alike, especially
the first two, and Capt. Carpenter, who was unfamiliar with
the species, speaks of them all as zetes acara. A. natalica,
Boisd., the commonest of the combination in British East
Africa (see the Rev. K. St. Aubyn Rogers in Trans. Ent.
Soc., 1908, p. 525), and egina areca, Mab., are not repre-
sented in this ex-German K. African collection. Capt. Car-
penter had taken acara and astrigera more recently than he
supposed, the first on Feb. 7, as well as Mar. 28, the second
on Jan. 9 and 10 (2), and Mar. 14.
“There have been lots of a Tabanid here with proboscis
about half-way between Pangonia and Tabanus, and I have
Gey)
caught a fine Pangonia [the g of a very striking new species]
feeding, hovering on the wing like a Bombyliud, from a Com-
posite flower. The specimen will be sent vou; I think it’s
not the same as the one which bit me” (Proc. Ent. Soc.,
1916, p. Ixxxn). Another Pangonia caught about the same
time is P. distincta, Ricardo, &.
* May 27, 1917. tigi.
“The operations in pursuit of a very elusive German force
in the neighbourhood are still in full swing. Some of the
‘W.A.F.F.s’ passed through here yesterday, and I saw a Hausa
for the first time. The commander of the force has been
taken prisoner, sick, but we have not had much success so
far, and the force still continues to run about, and gets lost,
and causes a lot of trouble. They cut our telegraph wire
this morning, and it is said they have put bombs on the
railway! I am much less busy now, as (following the usual
custom !) quite a large staff has been sent up here, now that
the work is about half what I had to cope with without
qualified assistance a little while ago. So I have been able
to get out for a bit, but we are now having very fine dry and
(in early morning) cold weather, which is bad for butterflies.
I am quite fit and enjoy the ‘cold mornings.
“ Pangonia is very common now, and I have caught
numbers of males. They often hover in the air exactly like
Syrphids (save that their long rostra are conspicuous), and
(with females sometimes) may be found on flowers. I caught
one male on a patch of white Labiate flowers, visiting flower
after flower, and putting his proboscis down each tube like
a bee! There was a very curious Tabanid here a little while
ago, with proboscis relatively about as long as that of Glossina,
a large blue-black fellow, with wings marked with bright
brown, who never made any attempt to bite, but was only
found on flowers or hovering in the air. [This is the new
Pangonia feeding from a Composite flower, v. supra. Three
females of another interesting Tabanid (Pangoninae),
Dorcalaemus compactus, Aust., taken Mar. 28, bore the note
that when flying their appearance and sound were very
bee-like.]
(ema 5)
* June 20,1917. Ttigi.
‘We are having very cold nights now—quite delightful —
I pile on all my bedclothes at night and even then feel cold
in early morning. I believe we are about 5000 ft. up here !
[4278°2 feet. |
“The party of Germans who were in the neighbourhood
are still uncaught, and leading us no end of a dance !
“| have been rather busy lately, as I have Smallpox to
deal with (as well as the usual Dysentery, Pneumonia and
Meningitis—I’ve got about 160 natives in hospital), and so
have been vaccinating and revaccinating all and sundry,
having to make a house-to-house visitation of the village
near here. Up to date not quite 20 cases—two (haemorrhagic)
died.
* July 9, 1917. Itigi.
“Still fine dry weather with cold nights.
* Continuing on Smallpox, IT had 19 cases, 9 of which died,
one of them vaccinated and with a few pock marks on his
face from childhood. It seems to have been a very virulent
form. The last man to develop it was only vaccinated 5
months ago—true, he did not get very large marks. What
with Smallpox and Meningitis I’ve seen quite a lot of the
more interesting diseases. There is still Plague which I
haven’t met yet ! |
‘Tam now rearing some Pierines from eggs, and have got
anege from Pinacopteryx simana, which is nice, as I presume
the larva must be undescribed, it having been so rare till
now that I have found it so abundant here. It has a well-
marked ‘dry’ form characterised by general suffusion with
browny grey scales beneath, so that resting among dry grass
it is very procryptie (as are other dry forms). Indeed I think
the explanation of the colours and shapes of dry Precis as
being procryptic receives great support from the marked
procrypsis of dry Pierines, Teracolus, for instance: the pink
or brown suffusion of the lower surfaces makes Teracolus very
hard to see among the. pinks and browns of dry grass, when
the wings are closed.
G ‘eva? >)
“ Aug. 9, 1917. Ltigi.
‘Tve got the cameelious hump to-night, so please be
patient and bear with me! The deadly monotony of this
place palls: I have only about 100 patients in hospital now,
and very few come to out-patients, so that, after my round
before breakfast and about 2 hours more after it, there is no
other medical work until the evening round—except some days
when I get some men to vaccinate, and then I do them at
the rate of 150 per hour, so they don’t last long! Very
different from the rather too strenuous times of a few months
ago when, except for very hurried breakfast and lunch-tea,
I was rushed from 7 a.m. to 7 or later p.m.! If only this
were Kakindu, and I could feel I was doing good insect
work! Now in the very dry time there is even less in the
way of Lepidoptera than ever—a few Pierines and occasion-
ally a Lycaenid or Skipper—so that one hardly feels it is
worth gomg out. However, I do go out in the afternoons
(or else I would fall asleep !), and to-day and yesterday got
three specimens of a nice Lycaenid [Rapala caerulea, H. H.
Druce, 3], on a flowering shrub, which was new to me and
cheered me up!
* About a fortnight ago [ had a very welcome change, as
I was sent away to a place called Lulanguru, about 17 miles
W. of Tabora, where one got back to the country of granite
kopjes and away from this infernal flat uninteresting bush.
There I found one or two species new to me—some fine
purple-tipped Pierines | Teracolus regina, Trim., g 9; also
T. ducissa, Dogn., 3 Q|, a Satyrine [Henotesia simonsi, Butl.],
a beautiful Lycaenid [probably the 3 Deudorix dinochares,
H. Gr.-Sm., see p. cxxxii], and, best of all, though not new,
I got four more Crenidomimas, which I haven't seen at Itigi.
So far as I could see they were the same as the ones I sent
you before. They came from the same kind of country,
and were also model-less! [see p. exiu|. It was also rather
nice to get away from the eternal (and infernal !) noisy railway
engines of this place. There is always one blowing off or
making a nuisance of itself in some way! Fancy being
( eviii_ )
worried with the noise of engines in the heart of Africa !
Well, well.
“ Well, that’s enough. I feel better now, thank you!
* Aug. 21,1917. tigi.
* Very little to do nowadays here. I think there is every
likelihood of this depot being closed, in which case I should
be moved somewhere else. I hope it will be somewhere as
far away and as different as possible from this dull, flat,
dried-up bush country as possible. Iam very bored with it.
* Aug. 22, 1917. tigi.
“T keep collecting P. simana on account of its bemg so
rare in collections : you may be able to use them for exchange.
I should like some to go to the B.M. Also I keep on collect-
ing other, commoner, Pierines (except the ones I know to
be universal), as they are now in the dry phase. There is
one very fine large Belenors [B. gidica, Godt.| of which f
only know the dry form with underside well suffused with
grey and brown scales. [The wet form was taken at Itigi
on Mar. 21, and 2 intermediates on Aug. 25.| It is more
agile and difficult to catch than any Pierine I know, which
is saying a good deal! I first saw it at St. Michael’s in
September of last year, and have never seen it since (7. e.
never during the wet season) until I got a fine pair in cop.
on Aug. 18th, and since then have seen several others. |
wonder if it only appears in dry weather ?
“On June 27 three of a handsome Lycaenid new to me
|Stugeta bowkeri, Trim., or very near this species], and on
June 28 and again on 29 a very lovely orange-pink Acraea
also new to me [A. acrita acrita, Hew., with reduced black
at the apex of fore-wing].
“On July 5 a very dead-leaf tailed brown Nymphaline
new to me. It flitted from bush to bush, taking especial
care to settle on or near clusters of wrinkled dead leaves.
[A 9 of Charaxes neanthes, Hew., 1854, the dry-season form
of zoolina, Westw., 1850. This form was also taken at
Lulanguru on July 24, Noy. 4 and 13, one of the specimens
being noted as “scarce.” The wet form zoolina was cap-
(a) crxa) 3)
tuted at mud, 4 examples on Jan. 7, near Ndala (32° 45’ E.,
2° 15’ §.), and 1 on Jan. 18 between Ndala and Igalula
(33° 15’ K., 4° 50’ 8.). The Pierine-like appearance of the
upper surface pattern of the wet form is specially noted by
Capt. Carpenter. |
“On Aug. 8 another Lycaenid | Rapala caerulea, H. H.
Druce, g| new to me, with a patch of purple suffusion in
middle of blue. Several more since then.
“IT found, dead, one evening, a lovely little Rodent which
I can’t place in my memory. I think it must have been a
Dormouse. Its head was rather rounded; it had mole-grey
fur, paler beneath, but its tail was plumose like a little
squitrel—erey, tipped with white. It was about the size of
our Dormouse.”’ Dr. Oldfield Thomas, F.R.S., writes that
the Rodent “would appear to be an African Dormouse—
Graphiurus—ot which many species are found all over the
continent.”
** Sept. 3, 1917. Ltigt.
“ Tt’s as dry as a bone everywhere, and except Pierines
there are no insects about. I have been much interested to
meet a dry season. I should not have believed there could
be such a difference so near the equator. It’s every bit as
marked, regarding insect life, as our Enelish summer and
winter.
Sept. 18, 1917. Itigi.
“ Well, [Pm still awaiting news about my leave being
granted. I am very much afraid that as the end seems to
be very near now, I may get caught in the process of clearing
up, which will be a lengthy business! I should think in
the end it will prove to be quicker to safari back from Tabora
to Muanza and go across the lake to Entebbe, rather than
to go down to Dar es Salaam, where one might have to wait
long for a boat to Mombasa !
SOcta 6,e19lia. ltign.
“Insect life is still very scarce. We are nearing the end
of the drought, and Iam watching with interest the sprouting
of bushes, etc., though we haven’t had a drop of rain to
( cx )
stimulate them. As regards Acraea caldarena f. neluska,
Oberth., you will, I hope, by this time have received a box
that contained some more of it and other butterflies. [This
refers to a rare form of caldarena, Hew., used in taste experi-
ments with monkeys at Ndala in Jan. 1917. Unfortunately
it did not appear in the later collections, but an Acraea taken
at St. Michael’s, Aug. 21, 1916, may be proved by structural
investigation to belong to this form.|
“Tve been trying to catch some Hymenoptera (as there’s
nothing else) for the Bureau, on Acacia flowers, and got
to-day for you a beautiful Hymenopteroid fly [a species of
the Syrphid genus Ceria (Cerioides) very near to gambiana,
Saund.|—brown and yellow with petiolated abdomen, and
wings longitudinally folded as in Diploptera which I have
never seen before. But the posterior half was folded upwards,
so as to lie on top of the darkened anterior half; the narrow
strips thus produced were held as a wasp holds them, so the
resemblance to a wasp of the type of Belonogaster was much
accentuated. [See also Dr. G. AY K. Marshall in Trans. Ent.
Soc., 1902, p. 534, and pl. xxii, figs. 40, 41; also Dr. G. B.
Longstaff in “* Butterfly-hunting in Many Lands,” pp. 392, 393,
pl. iv, figs. 1-10.| I also got there 3 lovely A. zetes acara,
typically Eastern : the E. form is even lovelier than the island
forms, and these were very fresh. [In the first half of Oct.
at Itigi 12 acara and 6 astrigera were taken. |
* Oct. 21,1917. Lulanguru (3766 ft.), on
Central Railway, 17 m. W. of Tabora.
“Since I last wrote I have been moved to a place where
I really can be of use and am not wasted as I was at Itigi.
My present camp, named Lulanguru, is where I was for a
brief period at the end of July and beginning of August,
viz. 17 miles west of Tabora: It is a flat, deciduous bush
country with granite kopjes. I told you something about
the place before : since my last visit the new green growth
has begun to come in readiness for the rains, and it is very
pretty and springlike. I was glad to leave Itigi, where I
was not at all justifying my existence and doing nothing to
help on the war, and I got very tired of the place and of the
( Se5sie sg)
noise of the railway and engines. My job here is to look
after a very large number of Congolese porters—15,000—who
will be sent through in batches. As they all come from
Sleeping Sickness country, and are going to a * Fly” country
(the rivers of G.E.A.), it is important that all cases of
Trypanosomiasis should be kept back. So I have to examine
each man to exclude S.S., and then vaccinate, etc. I am
quite glad to have a job of work again, and particularly to
feel that [am again in touch with * my friend the enemy,’ 8.8.
I hope at less busy times that I shall be able to send vou
some more butterflies from here, especially Crenzdomimas, as
before. So there’s no chance of leave yet, but I don’t mind
now that I have got a useful job to do.
** Nov. 2,1917. Lulanguru.
‘Tm very happy here now that I’ve got, at last, a job of
work to do again. Since the middle of October, when I got
here, three batches of Congolese of about 450 each have
arrived, and I have examined all of them and rejected some
for apparent early Sleeping Sickness. It’s very interesting
seeing natives of such different tvpe from what I have seen
hitherto—they are many of them very very small: these, of
course, are from the forests. It is said that altogether 15,000
are coming through here, but though that sounds a large
number it’s only enough to make good the wastage of all
porters for one month! I have about 60 in hospital; every
batch that arrives leaves me with cases of Pneumonia and
Amoebic Dysentery, but thank goodness they seem free of
Cerebrospinal Meningitis, which has been a great scourge in
some parts.
* Our local war is so far away (some hundreds of miles !
IT am 17 miles W. of Tabora) that we only know what the
weekly official wire tells us, but the one we got this morning
announced such a haul of prisoners and killed that one’s
hopes rise again that after all it may be finished this year.
If they can’t get it done before the rains begin in January
they will have to wait until June at the earliest before they
can begin again! ”
Speaking of Itigi: “‘ Fortunately I found some thorn
( cx)
Acacias in flower, and bottled lots of minute Hymenoptera
for the Bureau. Many are very curious-looking Chalcids, and
one a veritable giant about an inch long: I had never met
with one more than half that size before. 1 wonder if it
will turn out new. |Dr. Marshall has not been able to deter-
mine the insect, but thinks that it is a Larradomorpha, of
which Capt. Carpenter had previously sent another fine
species. |
“ Here at Lulanguru I bag great numbers of things at
light. Has this curious fact ever been recorded, that on
different nights different species predominate? About a week
ago one kind of Melolonthid, later another, last night a
third, with two small Chrysomelids, and to-night, as I write,
numbers of small actively flying Carabidae of several species,
none of which have come on any previous night. 1 suppose
the explanation is that large numbers of one species come
out at approximately the same time from the pupa.
“ Nov. 14, 1917. Lulanguru.
“ The Itigi butterflies are mostly a long series of pairs of
Pierines in cop. :—P. simana, Belenois, and Teracolus, a propos
of what I wrote before (Proc. Ent. Soc., 1917, p. li) that
Darwin had said Pierine 22 carry 3 3. In all these cases
3 carried Q, save in one P. simana, which was probably a
mistaken observation. The only other things of interest from
Itigi were a number of very fine Mastern zetes, and sundry
minute Hymenoptera and beetles for the Bureau.
‘ Charaxes abound on the kopje and some look interesting.
* Hot and exhausting weather.
* Nov. 27, 1917. Lulanguru.”’
Extracts from this and other letters on Pseudacraea pogge?,
Dew., and its form carpentert are published in Proc. Ent. Soc.,
1918, pp. V—vill.
Writing of Charaxes: “I fancy I can spot mimics in one
case at least. This kopje here is the best locality I have
struck for them, except perhaps Kakindu, but then that was
a large forest, whereas this kopje top is only a few hundred
yards square.
( exin )
* Pretty busy in mornings now: we have about 2000 in
camp, and they arrived infected with measles, mumps and
chicken-pox. I feel as if I was in charge of a boys’ school!
But I can collect most afternoons. We are having heavy
rains now—heavier than I remember at this time last year.
* Nov. 30, 1917. Lulanguru.
“The only larva of P. simana escaped when it was too
late to get more, as I was expecting to be moved! A pity!
“Tam continuing to get Crenidomimas here, and have
now got 4 or 5 more specimens, all, so far as I can see, the
same as before. I haven’t seen a single model! I don’t
know why the model shouldn't be here. [Capt. Carpenter,
who is always interested in the success of a mimetic likeness,
will be delighted to know that only four days before he
wrote this letter, he caught the model Crenis pechueli, Dew.,
and labelled it as the mimic; also that he labelled two
unusually bright and fresh Crenidomimas taken in Port. EK.
Africa (p. exxiii) as “ Crenis.”’| P. leoncdas, F. (blue 8. form),
swarms! By the way, yesterday I saw a magnificent Ps.
boisduvali. trimenii, Butl., typically Eastern, high overhead
and so out of reach that all I could do was to break my neck
goggling up at it!! So that makes the third species of
Pseudacraea here. Poggei continues to be caught! also
Charazes !
* Dec. 7, 1917. Lulanguru.
‘“ T have got some Nymphalines here 7 cop., in all of which
the 2 carries ¢—a Precis [actia, Dist., dry f.], H. daedalus, F.
(twice), and Ps. poggei, Dew. It seems to me that 1 Prerinae
the 3 carries 2 and in Nymphalinae the reverse. In a single
pair of Lycaenidae (Tarucus telicanus, Lang)—the only one
I have noted—the @ carried the 3.”
Between Dec. 19 and Jan. 2 Captain Carpenter captured
4 more pairs of telicanus, and in all but one, with the
smallest female (carried by the male) the male was being
carried by the female, and the same was true of a single
pair of Axiocerses amanga, Westw. (Dec. 31), and of Alaena
interposita, Butl. (Jan. 1), as also of the Satyrine Yphthima
asterope, Klug (Dec. 11), and the Acraeine A. encedon, L.,
type form (Dec. 12). As this paper is being prepared for
PROC. ENT. SOG) LOND,, Ui, 1v; 1918. H
( ‘exiv )
the press the followmg note has arrived, written May 5, 1918,
at Isipingo, on the coast near Durban, where Capt. Carpenter
is spending his leave: “A propos of pairs i cop. I saw on
the 2nd something of considerable interest. A fine pair of
P. dardanus, Brown, flew by in cop., alighted close by, flew
off again, alighted and flew off once more, so that there was
no possible doubt whatever that the 2 cenea, Stoll, was
supporting the g, which remained passive with wings closed.
Of course I had no net, and so could not secure the specimens ;
but I think the observation of value as it is so difficult to make
out which sex carries which in Papilioninae, and one doesn’t
often see Papilios i cop.”
[The specimens from Isipingo (1918) have now arrived and
include the following pairs of Pierinae, in all of which the
male carried the female: Hyronia cleodara, Hiibn., May 13;
Teracolus omphale, Godt., May 11; Belenois gidica, Godt.,
May 23; also a pair from Saranda, 7 m. N. of Kilimatindi,
ex-G.H.A., Feb. 5; B. severina, Cr., May 13 and June 6.
In addition to the Pierines the Nymphaline Byblia goetzius,
Herbst., May 13, the male carrying female. From Ankwabe,
Port. E. Africa, 40° E., 13° S. (1918), the following very
interesting Acraeine pairs: 3 A. caldarena, Hew., the larger
female carrying the smaller male, Aug. 1, the larger male
carrying the smaller female, July 29 and 31; 2 A. natalica,
Boisd., female carrying male in both, female distinctly larger
in one pair, Aug. 29, a little smaller in the other, July 31.
Also the Pierine Terias brigitta, Cr. (dry-season form), smaller
male carrying larger female, July 4, and similarly in a wet-
season pair from 34° 55’ E., 4° 40’ S., ex-G.H.A., Feb. 12.
From Monapo, Port. E. Africa, 30 m. due W. of the coast
opposite Mozambique Islands (1918): Acraea oncaea, Hopft.,
the male carrying the distinctly smaller female, Sept. 15;
Neptis agatha, Cr., the female carrying the much smaller
male, Sept. 11.|
[These results may be compared with those recorded by
the Rev. George Wheeler in “ The Entomologist’s Record ”
for 1918, p. 152. In the single pair of Dryas paphia observed
by Mr. Wheeler the male was carrying the female; but
Mr. H. Donisthorpe (“* Record,’ 1918, p. 171), Mr. Colthrup
(i texy )
(ibid. 1917, p. 246) and Mr. Wheeler himself (¢bed. 1917,
p. 166) have found both male and female taking the active
part. Mr. Hamm also saw, near Winchester (July 1896), a
male paired with the valesina female, and the latter, which
could not be mistaken, supported the former. More evidence
is required for all groups except the Prerinae. For these
Dr. Dixey’s conclusion on p. cli, will meet with general
acceptance. In this group, indeed, the males appear to take
the active part even when smaller than the females. |
Returning to the letter of Dec. 7: “ We have just heard
unofficially that von Lettow, the enemy commander, with
what forces are left him, has got across the Rovuma R. into
Portuguese East Africa. I’m not sure that it’s good news,
although it now means that the country is free of Germans,
all the other bands having been accounted for. But the
affair won’t be over till the gallant von Lettow is also
accounted for. He certainly is to be admired for his spirit.
* Dec. 9.—Sunday. Thundering and raining now and very
cool!”
The following acccunt of Lulaneuru, written for the Ento-
mological Society, was sent with the above letter of Dec. 7:
“This camp, 17 miles west of Tabora, is on the Central
Railway and also on the main road from Dar es Salaam to
Ujiji, along which countless slaves must have gone down to
the coast in old days, and up which Stanley may have come
to Ujij. It hes in country which I am told by a Rhodesian
is much like parts of N. Rhodesia. It is flat, 1148 metres
above the sea, with scattered irregular low hills and kopjes
of granite. The bush is of the open kind with small, not
thorny, deciduous trees, now in full spring leaf, and the
grass 1s sprouting again, so that everywhere it is delightfully
green. We had about a week of quite heavy rain a little
while ago.
“My collecting ground here is on a kopje immediately
behind the camp, which seems to concentrate insects from
the surrounding flat country: at any rate, until I started
collecting on its summit I never found anything worth much.
‘T will first go through the successive groups of butterflies
and then give a few notes on other Orders.
( exvi )
* Papilioninae.—1 very soon found there was a handsome
species [P. antheus nyassae, Butl.| here, new to me, reminding
me of policenes, Cr., but appearing paler, and with longer
tails. Curiously enough I do not find its tails nearly so
brittle as in policenes, of which it is hardly possible to take
a perfect specimen out of the net.
‘“T suspect this species to be a Southern form, as I have
never seen it before : it is a beautiful, Oriental-looking thing.
“ P. leonidas, F., is very common. It is of a blue form,
and thus new to me, as | have hitherto only met the greenish
form of Uganda. It has favourite spots over which it will
soar backwards and forwards [see 8. A. Neave in P.ZS.,
1910, p. 68], and if one is caught, another will almost at
once haunt the same spot. I have not seen its model
here.”
Capt. Carpenter’s specimens entirely confirm his statement,
being distinctly bluer than those from further north. I
remember that this point was raised inferentially in a letter
written to me from Katanga or North-East Rhodesia by
Mr. 8. A. Neave. In it he maintained that leontdas was a
mimic of an Amauris of the type of hyalites dannfelti, Auriy.,
rather than of Tirumala petiverana, Dbl. and Hew. He
referred in his letter to the apparent blueness of the former
in the wild state as being very different from its black-and-
white appearance in the cabinet. In his paper published
later in the Proc. Zool. Soc., 1910, p. 8, Mr. Neave says that
the transparent spots of the model’s fore-wing, ** due perhaps
to their more or less green background in nature, look pale
green on the wing.” But in writing to me I distinctly
remember how he emphasised the blueness.
Mr. Neave kindly wrote on March 29, 1918: “ Yes, I
recollect that examples of P. leonidas from Uganda were
greener than those from North-Eastern Rhodesia and Katanga.
I have no definite recollection about this species in German
territory. Iwas there such a comparatively short time that
I may not have taken it at all. I think I originally wrote
you ve the apparent blue or green colour of the white patches
of Amauris from Katanga, as this was the first locality m
which I had seen examples of the Amauris of this group m
( exvir, 4)
life. The apparent colour varies from blue to green with the
background.”
Mr. Neave wrote again a few days later: “I have had a
look at the B.M. series, and it seems probable that examples
from the drier parts of Africa are mainly of the blue type as
compared with the greener ones from more humid localities.
Tam not sure that the point is of great importance, though
the apparent colour in the Amauris models varies with back-
ground, being greener in shade and amonest vegetation and
bluer in bright sunshine; they would therefore appear more
often of the latter colour in drier and more open situations,
in which, however, they are comparatively rare.”
Capt. Carpenter continues : “ Papilio (Cosmodesmus) pylades
angolanus, Goeze, abounds : it is a curious-looking thing on the
wing, and sometimes as it dashes past has rather a Pierine
appearance. P. demodocus, Esp., is common. I have seen a
3 P. dardanus, Brown; somehow it looked slightly different
from the forms I knew on the islands in L. Victoria, and I
am wondering whether it also is from the south [probably
the Eastern form with a much heavier submarginal black
band to hind-wing]. It will be interesting if I can get a
female, for since I came here in October I have not seen a
single species of its models, and I have collected almost
every day. Presumably cenea [probably hippocoon, F.| would
be the commonest form. These five are the only Papilionines
I have met as yet.
* Pierinae.—I know so little of the names of these that I
cannot say much about them. Belenois and Catopsilia (the
thing like a Brimstone) are not very common—lI haven't
seen either HMronia leda, Boisd., or cleodora, Hiibn., here.
A Terias of a form strange to me [7 regularis, Butl.; see
pp. el, cli] is plentiful, and a few fine large Teracolus [7 casta,
Gerst.| not uncommon, but the feature of the Pierine fauna
is a magnificent large, fragile, pure white species with steely
purple tips to fore-wing [Teracolus regina, Trim.|. It is of
extremely powerful flight and is very shy, and therefore
almost imposs:ble to catch except when lulled by clouds or
in the evening.
“ Of Nymphalidae there are some good species. It is a
( cxvii )
marvellous thing that since I came here I haven't seen a
single Danaine of any kind whatever! [A 9 D. chrysippus, L.,
of the type form was taken a little later, on Dec. 31.]
‘* Acraeinae.—These have not proved to be plentiful : there
are one or two species that I never met until I had come a
good way south of the lake, and imagine they must be South
African forms. A. zetes, L., occurs in its typical Eastern form
[acara, Hew.| with yellow suffusion and very little black.
|The Lulanguru species was not acara, but anemosa (11) with
a single astrigera.| It is thus more lovely than the forms I
met on the islands. I find it extremely shy and difficult to
approach—far more so than such an aposematic and tough
insect need be! Iam quite sure that the Hastern forms I
have met are far more difficult to catch than the island
specimens were. A. encedon, L., occurs—rather washy and
uncertain in colour. It annoys me because I have never
found its larvae, and yet one sees it in all kinds of country,
so it must feed on some universally distributed food-plant.
|The larvae feed on the water-plant Commelina, “ Sudd.”
The Lulanguru collection contains—taken between Nov. 22
and Dec. 24—2 gg and a § and @ in cop. of the type form,
and 6 ¢ 3 of the form daira, Godm. and Salv. Thus the
daira form was not nearly so predominant as in Capt. Lam-
born’s collection made further east and north; Trans. Ent.
Soc., 1917, pp. 327, 328.]
* Nymphalinae.—Charazes abound on the kopje and several
forms are new to me. It is a wonderfully exciting spectacle
for an entomologist when these magnificent creatures chase
each other in the bright sun through the trees with their new
greenery. I saw one day a never-to-be-forgotten sight—two
species whose names I know not chasing each other, both in
perfect condition, one with the basal half of its wings sky
blue, the rest black [the g bohemanni, Feld.|, the other with
a broad border of rich terra-cotta to its velvety black wings
[the 3 azota, Hew.|. I put down rotten bananas as bait
(remembering Swynnerton’s tip) and have taken about a
dozen different forms, though how many species I know not.
The above-mentioned blue one, in 2, has a very conspicuous
white bar on the underside of the f.-w., which Iam certain .
( -Gux,)
_actsS as an aposeme when it 1s feeding [a note to this effect
accompanies a 2 bohemanni of Dec. 4]. It is resembled by
a much smaller species [the manica,* Trim... 2 of etheocles, Cr.].
A specimen of the commonest small species [guderiana, Dew. |
was once caught by a large Asilid flv, Just as it was fluttering
round the bait: this speaks well for the power of the Asilid.
I am sending prey and captor.”
Alcimus alamanus, Walk., Q with the 3 of Char. guderiana,
Dew., Nov. 12,1917. The Asilid bears the note “ probably
caught as it was fluttering round bait or on it, but I did not
actually see it in act.” Capt. Carpenter also sent a male of
the same predaceous fly together with the ¢ of Char. achae-
menes, Feld., captured by it Dec. 13, 1917. Both butterfl’es
are included in the table on p. exxi.
Capt. Carpenter not only recognised the mimetic resemblance
of the manica 2 to the 2 bohemanni—the note *? mimic”
appears on 4 examples of the former and “? model” on an
example of the latter taken with one of them on Nov. 20—
but he also noted the resemblance of the females of achaemenes
and guderiana to both sexes of saturnus, Butl. Examples
of each female and a male of satwrnus, taken Nov. 17, bear
the note “*? mimetic relation : same spot and time.” These
and other records of the three species on the top of the
kopje at Lulanguru afford valuable independent testimony
to the validity of Dr. Marshall’s suggestion (¢bid., p. 505).
These captures at Lulanguru in one limited area, of mimetic
Charaxes and their models among the larger species of the
same group, are recorded in the tabular statement on p. cxX1.
I have included the 9 azota as a probable mimic of both sexes
of varanes vologeses, R. & J.
It is probable from Capt. Carpenter’s experience that the
manica & of etheocles occurs where bohemanni is abundant
and its female—more conspicuous than the male—commonly
seen. Where this large species is scarcer the 3 probably
becomes a more advantageous model than the more rarely
seen 9, and manica is replaced by the phaeus, Hew., 2 of
be
the same species.| To test this conclusion we need from
* See footnote on p. Ixxx.
+ This paragraph requires revision in the light of Mr. Dollman’s
recently published evidence. See footnote on p. Ixxx,
(ex)
other localities where bohemanni is a model such facts as are
now recorded for Lulanguru, or such as Mr. 8. A. Neave.
the Rev. K. St. Aubyn Rogers, Mr. C. F. M: Swynnerton
and Major C. A. Wiggins have made available for other
forms of the 9 etheocles and their models. The phaeus f. is
recorded from Tabora, near Lulanguru (Rothschild and
Jordan, Nov. Zool., vii, 1900, p. 488), and Mr. St. Aubyn
Rogers took it at Mamboya (Proc. Ent. Soc., 1918, p. Ix),
while Capt. Carpenter captured an example on June 11, 1916,
far to the N.W. in the Ruanda Country, near Kigala. The
locality is described as open country in 30° 45’ E., 2° 10’ S.
The suggestion that the specimen is a mimetic 9 of etheocles,
new to the captor, was written on the “ paper.” Capt.
Carpenter was not sufficiently long in the locality to be able
to determine the existence or relative numbers of bohemani.
Further north in the strip of tropical forest near Kakindu
(Proc. Ent. Soc., 1916, p. cx) he took two examples of the
beautiful new ° form of etheocles described on p.1xxxii; also,
in the same forest, its model, the g¢ of a larger Charazes,
viz. etesipe, Godt. At this point it is of interest to record
his capture on June 28, 1916, in 31° 15’ H., 2° 40’ S., of a
3 Ch. hansali baringana, Rothsch., thus greatly extending
the known range of this rather rare form, described from
Lake Baringo, B.E.A., and taken by the Rev. K. St. Aubyn
Rogers in the Hills of Taita W.N.W. of Mombasa.
* Crenidomimas 1s not uncommon on the kopje, and now
that I have learnt its habits I have got a number, which
you will find interesting. It has a very skimming flight,
which is much like that of H. daedalus. The latter, of course,
keeps very near the ground, while Crenidomimas prefers to
fly 10 feet or more high, but it does not make long flights,
and returns over and over again to its favourite perch on
the extreme tip of a spray 6-12 feet above ground, so that
it can usually be caught. It often settles head downwards,
on tree-trunks, but is very very wary and extremely difficult
to catch in such a vosition.”
It is likely that the bu-terflies seen on the tree-trunks
were Cren's and not Crenidomimas. Mr. 8. A. Neave, with
a very extensive experience (Proc. Zoul. Soc., 1910, pp. 32,
)
XXi
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( exxn )
33, 38), writes: “I cannot recall ever having seen Crenido-
mimas settle on a tree-trunk, though the blue species of
Crenis, of course, do so often—generally rather high up. Most
of my examples of Crenidomimas that I caught settled were
on damp sand. As Carpenter says, they may often be seen
on the tips of boughs.” [The suggestion contained in this
paragraph has now been submitted to Capt. Carpenter, who
has replied that the first Crenidomimas taken by him (at
Namirembe Bay, July 27, 1916) was certainly settled, head
downwards, on a tree-trunk, and that at Lulanguru these
butterflies were captured at the flowers of a Papilonaceous
tree as well as on branches and tree-trunks. |
The Lulanguru collection contains 17 concordia—l 3 and
3 99 taken July 26-27, 12 gg and 1 9 between Nov. 19 and
Dec. 17. Six of the specimens are injured, probably in most
cases at least by enemies. It has already been stated (p. exiu)
that a single example of the model Crenis pechueli was taken
on Nov. 26. <A @ concordia was captured on the following
day, a ¢ on Nov. 28, and another on Nov. 29. The
occurrence of Crenis pechueli at Lulanguru extends its range
considerably to the N. and E., the localities given by Auri-
villius in Seitz bemg Congo [probably only the S.E. of the
State], Angola, Ovamboland, and Upper Zambesi.
Mr. Neave writes: ‘ C. concordia is a more widely spread
insect, both in tame and space, than the blue Crenis. The
latter are not only decidedly local, but are only on the wing
for a relatively short time. On the other hand, when they
do occur they are much more numerous than I have ever seen
C. concordia. 1 know of many places in Nyasaland where
the latter is not uncommon but where the Crenis are absent.
On the other hand, Carpenter can hardly be sure that the
Crenis are not present in his locality until he has spent a
whole cycle of the seasons there.”
In addition to the concordia from Lulanguru, Capt. Car-
penter took a 3 on July 27, 1916, at Namirembe Bay at the
S.W. corner of the Victoria Nyanza, and a ¢ and 9 Aug. 8-14,
1916, at about 32° 20’ E., 3° 20'S. The two latter resemble
the Lulanguru series, but the first and most northern differs
in exhibiting an orange-ochreous wedge in area 6 of the fore-
( oxxiii_ )
wing upperside—a feature which appears in a few of Mr.
Neave’s captures from much further south. This marking,
which is probably ancestral, deserves special study in long
series from as many localities as possible. No models were
taken with these three examples. The hind-wings of the
Namirembe ¢ are svmmetrically shorn, probably by a bird.
[Since the above was written a 9 concordia taken on July 31,
1918, in a dry stream bed at Ankwabe, Port. E. Africa (40° E.,
13° 8., about 1000 ft.), has been received (labelled ‘‘ Crenid ’’)
from Capt. Carpenter. The specimen, which is beautifully
fresh, exhibits an unusual development of yellow over the
basal half of the upper surface of both wings, especially
marked in areas 7 and 8 of the hind—a result which may
be related to the outlying locality on the E. fringe of the
range. Still later another fresh 2, also labelled ‘* Crenis,”
has been received from Monapo, Port. E. Africa, 30 m. W.
of the coast opposite Mozambique Islands (Sept. 13, 1918).
The basal areas are only slightly yellowish. |
Concerning these 3 C. concordia 1916 spoken of in the
last paragraph Capt. Carpenter wrote on May 20, 1917, from
Itigi: “I had rather suspected that the Crenidomimas was
amimic. Iseemed to remember a picture of it in Eltringham’s
book [* African Mimetic Butterflies,’ pl. vi, fig. 15]. I only
caught three or four, I think, and it was excessively wary
and not at all abundant. I did not ever see a model, but
as the country was in the dry period it doesn’t do to con-
clude that the model is not there. It was in very open
country, sometimes thorn bush, which is extremely bad for
butterflies generally. Didn’t I get some Crenzis in the Kakindu
forest? But probably not the species which the Crenidomimas
mimics.” [None of the blue species are in the Kakindu
collection. |
Capt. Carpenter’s account of the Lulanguru Nymphalinae
continues :
“The cream of the Nymphaline population at Lulanguru
is provided by my pet genus Pseudacraea. |The notes on
Ps. poggei, Dew., and the new form carpenter are published
in Proc. Ent. Soc., 1918, pp. v-xxii.|
“ To take the least interesting species first, lucretia [expansa,.
( cxxiv )
Butl.] is quite common. I fancy it is not quite of the same
form as the one I am used to on the islands [lucretia
lucretia, Cr.].
“ Ps. boisduvali trimenii, Butl.—l have to-day caught my
first specimen of this splendid Hastern form. It is certainly
much more like its model zetes acara |anemosa in the Lulan-
guru collection, see p. cxvii| (also of Eastern form here) than
the specimens I caught on the islands. Perhaps the vellow
suffusion in each case helps. [The ochreous subapical patch
on the fore-wing is well developed in this g example of
the Eastern trimenit.| This specimen was flying high, and
floating about in an exasperating way until it at last came
within reach of a vigorous swoop. Seeing that both trimeniw
and pogger exist here I shall keep a sharp look-out for imetator !
It would be splendid to get that too.
“The only other Nymphaline I have to mention from here
is a Precis of a form new to me which | think may be a dry-
season form [either archesia, Cr., or antilope, Feisth.| of one
that I have hitherto only met ‘ wet, but it is difficult to
carry the differences in one’s head without having specimens
for comparison. There was an interesting form |P. antilope,
Feisth., wet form simia, Wallgr.| which I first met with last
January : it continued abundant all through the rains, after
which it vanished, and has not yet put in an appearance
again: * it interested me chiefly because its underside very
closely resembled that of the wet or natalensis, Staud.,
form of P. octavia, Cr., though the upperside was very
distinct.”
Capt. Carpenter's collection made during his journey with
the Belgian Northern Forces and his sojourn at various camps
contains a most interesting series of 5 species of Precis in which
the seasonal differences are marked, and, in all except artaxia,
Hew., extraordinary. As so little is known of the butterfly
fauna of the area he traversed I have thought it desirable
to add on pp. exxvill—cxxxi a tabular statement of these five
* “ Since I wrote the above this Precis has appeared, simultaneously
with the wet form of octavia, Cr.: the coincidence is very striking.”
| Note added to duplicate copy of the account of Lulanguru, posted
Dec. 24, 1917. It will be seen in the tabular statement that the wet
form of octavia first appeared on Dec. 15, of antilope on Dec. 17.)
( exxv )
species as they were taken in the year and a half from June 6,
1916, up to Jan. 2, 1918. It is unnecessary to say anything
of the geographical forms of the species, which are of the
races characteristic of the 8. and EH. of Africa, except the
two following.
Precis archesia, Cr.—The wet forms (pelasgis, Godt.) are
on the whole intermediate between the most extreme wet
forms from further south in which the dark ground-colour
of the under surface is continuous and unmarked, and those
from the tropical north in which it is freely sprinkled with
grey scales (Trans. Ent. Soc., 1908, p. 546). Capt. Carpenter’s
examples exhibit a variable amount of grey sprinkling,
especially over the basal area of both wings. The outer red
transverse streak in the F.W. cell is distinctly represented in
grey on the under surface of nearly all the specimens, and is
usually accompanied by a much slighter indication of the
shorter basal red streak. Forms of pelasgis like these are
common both to the N., where they are accompanied by
“drier ’’ patterns, and to the 8., where they are accompanied
by “ wetter,” all being modifications of pelasgis with the
characteristic “ wet” outline of the wings.
The dry or archesia forms, as represented in Capt. Cars
penter’s collection, are remarkable in that they are never of
the full dry phase. The 10 examples taken June 13-20, 1916,
as well as the 2 of July 26, 1917, are all nearer to staudingert,
Auriv., than to any other form. The upper surface is of
the full dry phase, the under falling short in the nearly
uniformly coloured basal and, usually darker, distal areas,
diversified only by a wash of grey especially marked in the
distal area, and more strongly developed in the individuals with
a fuscous ground-colour, less in those that are brown. Thus
the appearance is very different from that of the intensely
variegated, highly procryptic, variable patterns which are
the commonest forms of the dry phase in 8. Rhodesia and
Natal: see Trans. Ent. Soc., 1902, pl. xiii, fig. 6, as com-
pared with fig. 7, which, although exceptional in Natal,
where it was captured, fairly represents the 12 forms of
staudingert taken by Capt. Carpenter. The basal area of a
single individual (June 15, 1916) bears indistinct reddish marks
( cxxvi )
approaching those of the examples taken Noy. 11-27, 1917.
These 9 worn specimens are nearest to semitypica, Auriv.,
and one of Nov. Il may actually belong to this form. The
others differ in opposite directions on the two surfaces, the
upper being wetter in the absence or very faint development
of the blue transverse streaks in the F.W. cell, the lower,
of a uniform dark brown in both areas, drier in the traces
of variegation caused by obscure reddish streaks in the basal
area, which in the F.W. follow the upper surface pattern ;
these streaks are only present on the H.W. of some of the
individuals, and here there is no correspondence with the
upper surface pattern. In one example of Nov. 11 the
reddish markings are accompanied by black streaks. It is
unfortunate that all these interesting forms are in such bad
condition.
Although, as Aurivillius states, both staudingeri and still
more semitypica are transitional in pattern towards the wet
phase, they are both very far on the dry side of intermediate,
the form of the wings—a difference far more important than
colour or pattern—remaining as in the full dry phase.
A single example of limnoria, Klug, wet f. taveta, Rog.,
from Itigi, Oct. 12, is omitted from the table. Aurivillius
keeps limnoria as a distinct species, but transitional forms
occur between it and archesia f. pelasgis, and the Rev. K. St.
Aubyn Rogers, who has taken limnoria in ex-German East
Africa and is familiar with it in B.E.A., believes that the
two are conspecific. Further breeding experiments and struc-
tural investigations are greatly needed, as also with pelasgis
in relation to coelestina, Dew. There is in the Hope Depart-
ment a series of specimens, collected at the N.E. corner of
the Victoria Nyanza by Major C. A. Wiggins, which includes
both wet and dry forms of coelestina and also butterflies
with the upper surface pattern of pelasgis, or its var. chapunga,
Hew., combined with an under surface apparently transitional
towards the wet forms of coelestina. Omitting the considera-
tion of limnoria, by far the commonest and in most localities
the only form of archesia in British Kast Africa and Uganda
is the wet-phase pelasgis, a little short of the full wet form
from South Africa. See Nov. Zool., xi, 1904, pp. 348, 349,
( “exxvil ~)
where Mr. Neave records 42 pelasgis from N.K. corner of
Victoria Nyanza, Entebbe and Toro: also Trans. Ent. Soc.,
1908, p. 546. Examples bred by the Rev. K. St. Aubyn
Rogers at Weithaga, B.E.A., were only slightly less “ wet”
than the parent (¢bid., pp. 545, 546).
Precis artaxia, Hew—The few examples of this species
afford an interesting contrast with archesia; for although
both appeared as wet and dry forms in the areas traversed
by Capt. Carpenter, archesia is represented by wet forms in
the tropical belt to the north, whereas all the specimens of
artaxia collected by Major Wiggins in the above-mentioned
locality were small dry forms, of which 42 are recorded by
Mr. Neave from Ugaia on the N.E. shore of Victoria Nyanza
(ibid., pp. 348, 349). Dr. Marshall and the late Capt. F. C.
Selous also observed the predominance of the dry form in
certain parts of S.E. Rhodesia and Portuguese E. Africa, and
it is probably adaptively connected with forested areas (Trans.
Ent. Soc., 1902, pp. 423, 439-41). Although the number of
specimens is so small, both nachtigall, Dew., and the more
extreme wet form mnobilitata, Thur., were taken by Capt.
Carpenter.
It is of interest to compare the remaining species of Precis
in the following table with Mr. Neave’s records from the
equatorial north (l.c.). Capt. Carpenter's actza, Dist., exhibits
both dry forms, actia, and wet, furcata, Rothsch. and Jord.,
while the 10 northern records are all of furcata. Mr. Neave’s
figures for octavia, Cr., also represented by dry and wet forms
in the following table, are unfortunately erroneous, probably
because the author had suddenly to leave England before the
proofs of his paper were corrected. Specimens recorded as
the dry form, sesamus, Trim., were examined and found to
be the wet form natalensis, Staud., by Miss Britten, who
has made a careful study of octavia in the Hope Department.
Furthermore, the large numbers of octavia, actia, and archesia
sent to me in more recent years from the neighbourhood of
Entebbe by Major Wiggins are all wet forms. Only in the
Tero Forest on the W. shore of the lake, near the old Anglo-
German boundary, do the dry forms of octavia begin to
appear, and this locality, although so near to Entebbe, has
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( exxai )
a very different climate with a regular wet and dry season,
as Miss Britten ascertained from the meteorological records,
and as Mr. Neave observed on the spot. Although octavia
appears to be always wet in equatorial Uganda and perhaps
in the extreme W. of B.E.A., this is by no means true of
B.E.A. as a whole, for many records testify to the existence
of dry forms (Trans. Ent. Soc., 1902, p. 447; 1908, pp.
542-44),
Precis antilope did not appear in the collection studied by
Mr. Neave, but both dry and wet forms occur in equatorial
B.E.A. (St. Aubyn Rogers, Trans. Ent. Soc., 1908, pp. 544-45).
Looking at the above tables it is seen that Precis oclavia ,
and P. actia follow the dry and wet seasons with precision
except for the presence of 2 wet forms of octavia in the first
dry period, and these, being worn, had probably lived for a
considerable time. The record of artaxia is very similar.
P. antilope, on the other hand, shows a strong tendency to
anticipate the seasons, both wet and dry, as is seen in the
group of wet forms taken Jan. 8-Mar. 21, 1917, and the dry
between Apr. 1 and July 25 of the same year, the latter
being mixed with wet forms towards the end of the wet
season. P. archesia follows the seasons except for a single
early wet form on Nov. 19, 1917.
* Salyrinae.—There is a species here on the kopje and
elsewhere that is new to me—a pretty fawn-coloured large
species | Henotesia simonsi, Butl.|. There are others (Yphthima,
etc.) here which are probably different from those I have sent
before.
Lycaenidae.—There are very few on the kopje, but when
here for a week in August I got a fine species new to me,
which you. have received previously to this letter—one of
those with the spots on the underside split. The male is of
a coppery brown colour [Deudorix dinochares, H. Gr.-Sm.}.
However, there are, I think, two other species here new to
me which I send now. One of them has a very boldly marked
underside [Spindasis homeyeri, Dew.|: it has its tails ab-
stracted by some enemy. The other is one of those rich
copper-coloured forms with red brown underside and very
short twisted tails. [Both Axiocerses harpax, F., and amanga,
( cxsan »)
Westw., were taken: a 3 harpax bears the note “ Oct. 26,
1917. Settled on me to drink sweat.”’| I have not seen any
of those lovely light blue species with long milky white tails :
I think they require forest and not open bush.”
Probably the most interesting Lycaenid from Lulanguru is
Alaena interposita, Butl., of which a long series of both sexes
was sent. It is certainly the species described and figured
as A. hauttecoewrt by Oberthiir in “ Etudes,” 12, p. 7, pl. 3,
figs. 7 and 9 (1888). The figures are, as usual in this great
work, admirable, and the examples described were from
Tabora, only 17 miles from Lulanguru. It is unfortunate
that Butler’s cnterposita, described in 1883 from a_ single
neatly female-coloured male from Victoria Nyanza, should
take precedence over Oberthiir’s name accompanying the
description and figures of the typical form. Aurivillus in
“ Rhop. Ethiop.,” p. 255, is mistaken in sinking Butler’s
Alaena aurantiaca—a very different species—-to the male of
haultecoeurr.
Two of Captain Carpenter's examples of the yellow male
bear interesting notes: “‘ Oct. 24, 1917. Acraeine mimic.
When unalarmed flight looks like small Acraea.” ** Oct. 27.
On stony kopje where long dry grass. Flight slow and
fluttering like Acraeine on wing. One specimen was bottled
as it sat on grass stem !!”
I take the present opportunity to correct the unfortunate
slip by which Telipna reticulata is quoted in place of Alaena
reticulata, in Proc. Ent. Soc., 1916, p. cxxv, 1. 4, and in the
footnote. Furthermore, comparison with the ¢ type of
A. reticulata in the British Museum proves that Capt. Car-
penter’s specimen does not belong to this but to a species at
present undetermined.
** Hesperidae.—Are fairly abundant. One (? Sarangesa) is
new tome. Of dark mottled grey, it rests on the bare granite
rock, flat, with wings outspread like a Geometrid, and is as
equally procryptic as the moths on bark. I have sent one
or two specimens.”
An example of Sarangesa motozioides, Holl., Nov. 7, 1917,
bears a note similar to the above. Four examples of Hagris
jameson, EK. M. Sh., of July 26-27, 2 of Aug. 1, and 1 of
( cxxxiv )
Nov. 5 are the yellowish dry-season forms; while 2 of
Nov. 5-9, and 3 of Dec. 26-31 are the black-and-white wet
form. Of these latter a pair taken in cop. on Dec. 26 were
resting with expanded wings on the under side of a large leaf.
Among the moths collected at Lulanguru was a most
interesting series of individuals hitherto regarded as belong-
ing to four different species of the Pterothysanid genus
Hibrildes. The occurrence of all together in the same locality,
and almost certainly on the same small kopje top, strongly
confirms the conclusion at which Sir George Hampson has
arrived, that all are forms of a single species. Of the 11
moths—all taken Dec. 1-31. 1917—3 are white males (noraz,
Druce); 3 are white but strongly veined males (venosa, Kirb.) ;
3 are Acraeoid females (crawshayi, Butl.); 1 is the form
with orange-ochreous hind-wings like crawshayi but fuscous
fore-wings with a white subapical bar (ansorgei, Kirb.). On
this Capt. Carpenter had noted ‘‘ On wing incipient Aletis or
chrysippus mimic.” The eleventh specimen is an interesting
variety of ansorgei with a rich orange-ochreous subapical
fore-wing bar.
“ After butterflies come moths, and that brings me to the
subject of insects which come to light. Moths are almost the
only things that don’t come here—I have never seen so many
insects at light. The most curious feature is the predomi-
nance of different families—or even species—on different
nights. Sometimes the table is covered with wood-borers of
numerous forms; on other nights quite small Carabidae; then
large and annoying Melolonthidae predominate ; on another
night Hlateridae, sometimes large, sometimes small; then
small Melolonthidae or Copridae, Mantidae, Blattidae, Myr-
meleonidae, a few Diptera, Hemiptera, Longicornia, Weevils,
water beetles of different groups, Gerris. Quite large and
very odoriferous Carabidae, Cicindelidae, and even a beautiful
Dragonfly and large Cicadas have all come. Perhaps on one
night several species of an insect will come which is never
seen again. Indeed Crustacea, Myriapoda, and Arachnida
are almost the only Arthropods that have not been attracted !
Consequently I have made a large collection for the Brit.
Mus., and send you duplicates whenever possible. I have
(@ (Cx u)
not yet been able to ascertain exactly what constitutes a
‘good dudu night,’ but it must be calm and warm, and I
think unsettled : a clear starlight night is not so good. How
interesting it would be to make huge collections every night
and correlate the different groups with minutely recorded
meteorological data !
‘** Now a few other observations from my journal.
“ Attractiveness of exudate from trees—On Nov. 11 and a
few days before and after I noticed a minute moist patch
about a centimetre square on the bark of a tree which was
very attractive to Hymenoptera and Charaxes. I caught
three specimens of brilliant green Ampulicinae of at least
two species, in succession, and Pompilidae also frequented it.
It was presumably caused by a fungus disease. Another day
a very sickly-looking stem of a sapling about 3 feet high
was so attractive to Charaxves that half a dozen specimens
of different species visited it at once, and probed-it eagerly
with the proboscis. After a day or two it proved less attrac-
tive, but some fine Cetoniidae came to it: when gum began
to exude it was no longer attractive.
* Mutilloid Spider.—\I sent you a year ago from Ndala a
Mutilloid spider [see p. xcvui], and now send a second specimen
like the first, with red thorax and black abdomen with four
large white spots. As in the first instance, it momentarily
deceived me as it ran along in a very Mutilloid manner.
But when alarmed it scurried away in a typically spider
fashion.
* Ammophila lugubris, Gerst.—I sent you some notes on a
very unskilful or inexperienced specimen of this Fossor from
Ndala, about a year ago | Proc. Ent. Soc., 1917, pp. xli-xliv,
where the specimen is referred to beninensis, Pal. de Beauv.|.
A species which seems the same is common here now. On
Nov. 26, on the kopje, as I strolled along, watching for
butterflies, I saw on a low shrub at my feet one of these
Ammophila behaving in a very curious manner. It was
straddling a small stem and every now and then excitedly
grasping it in its mandibles, as if if were a caterpillar. The
reason for this was soon seen, for after a few minutes she flew
to the ground at my feet and picked up her larva, which
(| cxxxvi )
she had dropped as I approached. This little point (grasping
the stem) is most illuminating, as showing how the several
acts are but links in a mechanical chain: the operations had
arrived at a point when the impulse to grasp something in
the mandibles was overwhelming. Having picked up her
Jarva she carried it belly upwards, holding it at about the
4th or 5th segment, so that its anal extremity projected
upwards in the air behind her, and walked with it for about
20 yards, keeping a wonderfully straight course among stones
and tufts of grass. She then turned at a right angle and
went on for another 10 yards, and then quite suddenly, as if
certain of her whereabouts, put down the larva on a small
clear space and began to take away the minute pebbles in
her mandibles. I could see no difference from the surrounding
soil, but the burrow was there right enough, for she very
soon disclosed its mouth by removing a clod of earth, and
went down, came up again, went down backwards, seizing
the larva (a smooth Noctuid) by one extremity (probably
anterior, but I forgot to take especial note), dragged it in:
then after a short pause for oviposition came out again and
started fillmg up the hole in the usual way, when I bottled
her for identification. If she is the same species as the Ndala
one she affords the greatest possible contrast in skilful work-
ing. |Mr. Rowland KE. Turner has carefully compared the
two specimens and finds that they are the same species,
which he thinks should be placed under lugubris, Gerst.,
until the relation between this and beninensis, Pal. de Beauv.,
is satisfactorily cleared up. |
“On the evening of Dec. 5th I saw in a shed another
specimen of apparently the same species, which I failed to
secure. She brought her larva (rather a smaller Noctuid
larva than those above recorded) into the hut and started
opening up her concealed burrow. Having disclosed it she
took out one or two small clods of earth and went down,
and reappeared with a Noctuid larva (of the same size as
the one she had just brought), which was rather unusually
wrigely at its hinder end. She brought out a little more
earth from the burrow, and then turned to this latter larva
und apparently decided it was too lively, for she proceeded
( exxxvi )
to massage it systematically with her mandibles from end
to end, passing from tail to head. Twice she left off for a
moment to push her face along the dusty ground, as if to
clean her mandibles from something that soiled them, although
she certainly had not broken the skin of the larva. I have
never seen a Fossor do this before. Eventually she put the
larva down with its head at the margin of the burrow, went
down backwards, seized the larva by the neck and dragged
it down, came out, went down and came up again with a
little more earth, did this twice again, and then dragged
down the larva which I had seen her bring in. My attempt
to bottle her failed. I had no net with me, and as I was
due at the hospital for the evening round I couldn't wait
for her return. But I’m sure she was of the same species
as the last. It’s interesting that she was using two medium-
sized larvae instead of one larger specimen.
* Courtship of Diptera.—The courtship of Asilidae which 1
have witnessed several times is an interesting performance.
The species referred to was almost certainly a Promachus.
The Q sits as usual on a prominent bare twig, and the 3
hovers in the air like a Syrphid, a few inches away on her
right or left front and a little above. His energies are appar-
ently directed to pleasing the lady by his hum: the pitch
gradually rises, and as it does so he no longer remains
stationary but oscillates shghtly up and down, and then,
just as the situation gets very exciting, the 2 suddenly dashes
away and the ¢ after her. Sometimes she settles again and
the whole process is repeated, but I have never seen the
actual union. One very often sees pairs united end to end:
at other times the ¢ is on the back of the 9, who often has
her proboscis embedded in some prey [see Trans. Ent. Soc.,
1906, pp. 366-68], but whether the latter position is previous
or subsequent to the former I do not know.
“In another group of flies, Bombyliidae, the g also en-
deavours to please by his hum: in this case I have caught
a specimen for identification [a Q Hxoprosopa eluta, Lw.].
On Nov. 29th I first saw this. It is a species which keeps
close to the ground, on which it often settles. On this ocea-
sion I saw one, presumably the 9, sitting on the eround
( exxxvii )
while the other slowly circled round her, slightly above,
making a most peculiar hum in which there was something
of the rattling noise made by the large * clockwork > Pompilidae,
but can be best described as like the noise of an aeroplane
heard fairly high up. Here again the 9 darted off just as
things got exciting. I saw another couple on a subsequent
day, and was very anxious to net the hummer to prove it
was a o, but I couldn’t get it apart from the other. I
noticed on the second occasion that the sitting specimen
vibrated its wings slightly also.
* Chlamys marshall, Jac. (Chlamydinae, allied to the Crypto-
cephalinae).—On Dec. 3rd I got a most curious beetle which
I am sure is specially procryptic. It is a small, square, solid
little insect with no limbs or antennae visible, and no con-
strictions visible between head and thorax or thorax and
abdomen. It is of a greenish brown colour with rough
integument. It was sitting on a vertical stem, closely apposed
to it, and when I saw it I thought, ‘ Why does that caterpillar
excrement remain on a vertical stem?’ For that is precisely
its appearance. It was not till I examined it very closely
in my hand that I realised it was a beetle, and had it been
resting on a horizontal leaf I should certainly have looked for
a large caterpillar! I hope you will find it in the box and
identify it.
“One more observation—quite a small one, but rather a
curiosity. I was at a flowermg shrub visited by many
Hymenoptera, among them one of the large * clockwork ’
black Pompilidae. It flew high over my head, but as it
went about was closely followed by some half-dozen smaller
black Hymenoptera, that might have been Scoliidae, just as
small birds mob a big one. I can give no explanation, and
am much puzzled by it.
* Jan. 1, 1918. Lulanguru.
“ With reference to this box, No. 5 [containing Lulanguru
captures of Dec., 1917], there are in it some nice, small
Braconoid and Lycoid Longicorns, the former of which have
absolutely deluded me in the field! I watched one quite a
long time flying among some twigs and said to myself, “ Ah !
CPexxxix)
you are the Braconid which the last Braconoid which deceived
me, mimicked !’ and, lo and behold, it was again the Longicorn
in my net!”
Capt. Carpenter’s collection, especially from Lulanguru,
contains many interesting additions to the great Lycoid
combination described and figured by Dr. Marshall from
Salisbury, Mashonaland (ibid., pp. 515-18, pl. xviu, figs. 1-52).
The abundance of the central models at Itigi was well shown
by the capture of 272 Lycidae belonging to 9 species, on a
single plant on Mar. 23, 1917 (Proc. Ent. Soc., 1917, pp.
Ivi—lix). These 9 species only contained 2—Lycus ampliatus,
F., and rostratus, L., and these in relatively small numbers
of the species figured by Dr. Marshall. The mimetic species,
of which a list is printed below, are all different from Dr.
Marshall’s except Amphidesmus analis, and the 3 species of
Dirphya (Nitocris); and upon the mimetic relationship of these
last Capt. Carpenter sheds new light. The locality is Lulan-
guru and the year 1917, unless otherwise stated.
Diptera (Tachinidae).—Paraclara magnifica, Bezzi., Dec. 25.
* Mimetic of Lycoid Fossor.” Also taken in the Ruanda
Country, 30° 35’ E., 2° 10’ S., on June 8, 1916, when a
similar note on the resemblance was recorded.
LeprpopTeRA (Tineidae).—Oedematopoda princeps, Z. (allied
to Hyponomeuta), Dec. 17 and 19. ** Lycoid at rest ”’ noted
on both specimens.
HEMIPTEeRA (Capsidae).—Lycidocoris mimeticus, Reuter and
Poppius, Nov. 21 and 26. “ Beautifully Lycoid on wing”
and “* Very Lycoid at rest’ are the respective notes.
Hymenoptera (Larridae).—Notogonia bembesiana, Bisch.,
Jan. 14, 1917, Ndala. ‘‘ Lycoid Fossor.”” Mr. R. E. Turner
informs me that this species bears a close resemblance to a
much commoner and more widely ranging Fossor, Liris
haemorrhoidalis, F.
Hymenoptera (Tenthredinidae).—H ylotoma (Arge) annulipes,
Klug, Nov. 21 and Dec. 4. “* Lycoid at rest” on both.
The Hymenoptera Parasitica are considered later, as Capt.
Carpenter shows that they play the part of models as well as
Lycoid mimics.
CoLEorTERA (Cetoniidae).—Glycyphana (Gametis) balteata,
( sexk--)
de G., Dec. 5. ‘‘ Lycoid.” This mimetic resemblance and
the association with Lycidae in life was noted by Dr. Longstaft
and Dr. Dixey (“* Butterfly-hunting,” pp. 237, 238, 241).
CoLeopTERA (Telephoridae).—Ichthyurus sp., Dec. 6 and 13.
No note is added to this species, but I think there is no doubt
that the pattern is Lycoid, although the colourimg of the
anterior parts is rather too bright and yellow for a perfect
resemblance. It is possible that the insect is Braconoid on
the wing.
CoLEopTERA (Longicornia. Cerambycidae).—Amphidesmus
analis, Oliv., Dec. 23. “* Sitting on grass-blade very Lycoid.”
Included in Dr. Marshall’s list and shown in his pl. xviii,
fig. 25.
CoLEoPTERA (Longicornia. Ceraimbycidae).—Apiogaster or
genus near it, not in the British Museum Collection, Dec. 24.
* Beautifully Lycoid at rest,” in spite of the fact that the
head and thorax are entirely black as well as the apices of
the elytra.
CoLeopTeRA (Longicornia. Lamiidae, Phytaecinae).—Mys-
trocnemis bicolor, Auriv., Dec. 24.“ Very Lycoid.” In this
beetle, as in Glycyphana balteata, the Lycid pattern is reversed,
being black anteriorly and orange-ochreous posteriorly. Capt.
Carpenter's note that both these beetles are Lycoid confirms
Dr. Longstaff’s conclusion that this reversal probably does
not detract from any benefit that the Cetonid may derive
from the likeness (¢bid., p. 238).
Capt. Carpenter brings evidence that the remaining Longi-
corns (all Lamidae, Phytaecinae) of this combination are
Braconoid when flying although Lycoid at rest. Of the
models for the two larger species Dirphya (Nitocris) nigricornis,
Oliv., and similis, Gahan, only Pseudobracon sevillei, Brullé,
Dec. 5,—a Braconid in spite of its name—appears in the
Lulanguru collection. It bears the note that the large
Dirphyas in the same box * look much like this on the wing.”
The pattern of this model is that of Phaneromeris sp. figured
by Dr. Marshall on his pl. xviii, figs. 44, 45, while the two
Lulanguru mimics enclosed with it are represented in figs. 29
and 30. A 3 specimen of D. nigricornis, Dec. 14, 1916,
Ndala, bears the note ** Most extraordinarily like Braconid
( cxli_ )
on the wing,’ while another ¢ of Nov. 29, 1917, and a ¢
D. similis of Dec. 23 bear no special note, but are the specimens
referred to in the label of the Pseudobracon.
A smaller Dirphya (Nitocris), of still greater interest, was
also included as a Lycoid by Dr. Marshall, and represented
as Nitocris sp. in his fig. 28. It appears to be still undescribed,
although specimens from Damaraland, Nyasaland, and Umtali
exist in the British Museum. <A ¢ of Dec. 17 bears the note
“ Caught on wing as a Braconid,” and a Q of Dec. 24, with
* Completely deceived me. Caught as a Braconid on wing,”
is probably the specimen referred to in Capt. Carpenter’s letter
of Jan. 1, 1918 (p. exxxviii). The former specimen set with
expanded wings shows that the distal black and basal pale
orange-ochreous area of the elytra are continued on to the
functional wings, which therefore bear a pattern. This is
very rare in beetles, and Dr. Gahan and Dr. Marshall are as
sure as it 1s possible to be without making a special study
of the point that all the African Lycidae of this combination
have uniform, dark lower wings. The appearance is clearly
mimetic of Braconidae during flight, and affords the strongest
confirmation of Capt. Carpenter's conclusions, with which
Dr. Marshall tells me that he entirely agrees.
Since the above paragraph was written a specimen of each
of the larger Dirphyas, nigricornis and similis, has been set
with expanded wings, showing that in these too the elyiral
pattern is continued on to the functional wings. Further-
more, there were marked differences between the concealed
patterns of the two specimens which may be characteristic
of the species.
The most perfect models for the small Dirphya are doubt-
less Bracons with patterns like those shown on figs. 44-46 of
Dr. Marshall’s pl. xvii, and especially the two smaller forms
represented in figs. 47 and 48. None of these were sent by
Capt. Carpenter—although, as already mentioned, the Pseudo-
bracon possesses a similar pattern—but he included a Braconid
of the genus Glyptomorpha, Dec. 351, with a pattern like that
of the Braconid and Ichneumonid represented by Dr. Marshall
in figs. 59-61; also another smaller Braconid of the genus
Merinotus, Dec. 17, with a less emphasised form of the same
Cex) >)
pattern. These would doubtless serve as models when on
the wing, but there can be no doubt that smaller species
with the pattern of the Glyptomorpha exist in the locality
where the Dirphyas were taken. Dr. Marshall shows in
fig. 62 a Reduvid bug with the most wonderful mimetic
likeness, at rest as well as in flight to the Parasitica of figs.
59-61.
From these last species of Dirphya, Lycoid at rest, Braconid
in flight, we pass to two species of the allied Lamiud genus
Oberea, of which the first is doubtfully Lycoid, the second
certainly not, being Braconoid at rest as well as in flight.
Two males of the first, O. sp., probably ventralis, Gahan,
taken Noy. 22 and Dec. 26, both bear notes recording that
they were “ caught on the wing as Braconids”’; a third male
of Jan. 1, 1918, was “ very Braconoid on wing.” The pattern
is very similar to that of the Dirphyas save that the anterior
orange-ochreous is so much reduced that any direct mimetic
likeness to the Lycidae is doubtful, although a place on the
outskirts of this dominant combination is probably advan-
tageous. In the second species Oberea sp. very near scutellaris,
Gerst., g, the pattern is similar but the anterior colouring
red instead of orange-ochreous, bringing about a close resem-
blance, especially on the wing but also at rest, to the black
and red Braconidae. The beetle was “taken for Braconid
on wing,” the model, a species of Iphiaulax near coccineus,
Brullé, being sent with it, both captured Apr. 15, at Itigi.
Three species of Braconidae with this pattern, including
coccineus, together with the mimetic Oberea scutellaris, Gerst.,
and Reduviid bug Callilestes bicolor, Dist., are described and
shown by Dr. Marshall on p. 533 and in his pl. xviii, figs.
53-8.
The resemblance of Bornean Longicornia to Braconidae is
dealt with in detail by the late Mr. R. Shelford, who gave a
list of 12 species of Phytaecinae, including 9 Obereas, that
are mimetic in this way (Proc. Zool. Soc., 1902, pp. 238-40).
The next letter, written in January from Dar es Salaam,
gave an account of a visit to Lake Tanganyika after Capt.
Carpenter had been relieved from his post at Lulanguru :—
* Here I am at last in Dar es Salaam, with, so far as I
( Foxit }
ean see, no prospect of getting home until months after all
activities have come to an end. It’s not in any way an
attractive place, and every one dislikes it. J am in charge
of the West African section of the huge carrier hospital here,
and shall apparently remain so. I may get some local leave,
but no home leave is being given. IT arrived here on Jan. 15th
after a most enjoyable week visiting Tanganyika, and think
the Entomological Society might like to hear something of
the lake, so I write this account.
“ Having been relieved of my last job I obtained unofficial
leave to be absent for a week, and left Lulanguru at 7 p.m.
on Jan. 3rd in a very comfortable, first-class coach, and at
daybreak found the train just beginning the descent to
Tanganyika, among hills well wooded and interesting, because
all the vegetation seemed different from that at Lulanguru
and also from that around L. Victoria. I noticed Bamboos
and what I took to be giant Lobelias, though of a species
different from the one I had met at Kigezi. I saw, before
it was really light, some huge dark animal moving away
from the railway, which I took to be a Rhino.—the first I
have seen. Incidentally also it was the only Mammal I saw
on the journey to Kigoma and back from there the whole
way to Dar es Salaam, although one night was spent in
travelling —rather a remarkable difference from the teeming
herds of game to be seen from the Uganda Railway. Well,
as we got nearer I saw the lake in front of and below us,
very black and stormy-looking, with the mountains of the
other side clearly visible; on our right, to the north, a rugged
range of bare rocky mountains was flooded with golden light
from the rising sun, and the whole effect was rather
magnificent.
‘We reached Kigoma, which lies at the head of a well-
sheltered bay, at 7.30 a.m. on the 4th. Though prettily
situated it is not itself a pretty place. The northern coast
is formed by low hills covered with green bush, affording a
pleasing contrast with red soil and blue water. Most of
Kigoma lies on the south side, so that there are no trees or
bushes worth mentioning. There are only three large build-
ings, one a hotel and two Government blocks. At the south
( exhv )
s.de of the bay is a headland of a formation quite different
from the north, consisting of small rounded boulders and
large pebbles embedded in a loose matrix.
“Shortly after arrival I wandered along the shore and
found numbers of the fresh-water jellyfish cast up on the
sand, in diameter about equal to a florin or half-crown, and
so absolutely colourless that I never succeeded in finding one
m the water. I also found numbers—but all water-worn—
of one species of the molluscs peculiar to Tanganyika, a
large conical species some three inches in height, and a single
specimen of a tuberculated shell like the marine Nassa.
There were also single valves of Lamellibranchs with marme
appearance.
which lies 7 miles south of Kigoma, the country in between
all cultivated. I was much disappointed in Ujiji: as it is
an old Arab settlement I had expected to find it picturesque,
but it merely consists of great numbers of square mud houses,
dirtily whitewashed, with thatched roofs, swarming with
children. The famous meeting-place of Stanley and Living-
stone in 1871 is marked by a block of concrete under an
old, decrepit mango tree, formerly, at the time of meeting,
on the shore. Owing to the shrinking of the lake, like the
other African lakes, this point is now some 200 yards distant
from the present actual shore, and I should think some
20 feet above it. Hence between 1871 and 1917 the lake
has fallen 20 feet. When one realises that 6000 feet have
been sounded without touching bottom (authority, Commander
Thornley, R.N., in charge of our boats on the lake), one
wonders what is happening that such a prodigious volume
of water should fall in level at the rate of about 5 inches a
year !
“On the morning of Jan. 5th I wandered along the shore
of the bay looking for objects of interest, and got a fine
Cicindelid [C. regalis, Dej., also C. intermedia, Klug] new to
me. I may say here that almost all the beetles [including
the Coprid Onitis wncinatus, Klug, 3| and Hemiptera I saw
were strange to me, also some moths, but the only butterflies
seen were familiar. I obtained a few specimens from both
(Scxlva ~ )
sides of the lake which may be of interest to the Kntomo-
logical Society. On this morning I saw and obtained a fine
Pompilid [Psammochares irper, Gerst.| quite new to me,
apparently specialised for digging in very loose sand such as
Bembex also loves, for, like Bembex, it had the fore-limbs
set closely with large bristles much more abundantly than
those of other Pompilids which dig in hard soil. It is obvious
that a brush-like leg is much more suitable when the sand
is soft and loose. This species, which I send you, is grey
and black, with wings approaching the Lycid coloration.
I first saw it running quickly about, obviously searching for
something, and soon it came to a spot where it scratched
away a little loose sand and laid bare a spider, paralysed,
and apparently hidden away until the wasp had found a
suitable spot in which to bury it (this is a trait I have not
met before among Fossors). The wasp then took it up and
ran backwards with it for a good many yards, only occasion-
ally turning round to negotiate a difficulty, until she came
to the spot where the burrow had been previously dug: for
she put the spider down, took away a lump of sand, and laid
bare a very shallow hole into which she put the spider,
without going down herself, and quickly covered it up with
loose sand.
‘On the evening of the fifth I embarked on a small tug,
which had done 12 years’ service on the Congo, and was
bound for Albertville, the port which the Belgians have made
on the west side of the lake, where the Lukuga river, one of
the main sources of the Congo, takes origin. Since the war
began the Belgians have made this port and run a railway
to it, so that now one can cross Africa from Dar es Salaam
to the mouth of the Congo by rail and steamer alternately.
This Albertville is a new place: the former Albertville (now
known by its native name of Toa) lies some 20 miles north-
wards. After a night of oily calm I awoke just before dawn
to find that we were passing the most prominent point of
the western coast (which lies S.8.W. from Kigoma), steaming
between the mainland and a few small islands very close to
the shore, rocky, and densely covered with bush, reminding
me very much of islands of the type of Ngamba in L. Victoria,
PROC. ENT. SOC. LOND., II, Iv. 1918. K
( -exlyva_)
The mainland has ranges of hills rising one behind another
to a height of about 3000 feet, for the most part well wooded,
but sometimes bare. Toa was soon passed—a few houses
prettily situated on a low hill with its base lapped by the
lake. Between this hill (which not long ago must have been
an island) and the mountains is a stretch of flat sand over-
grown with bushes: part is still under water, and forms a
lake or lagoon which was used by Belgian hydroplanes in
July, 1916, as a base from which they bombed the Germans
out of Kigoma with great success. As we drew near the
source of the Lukuga the coast became flatter, and there
were long sandbanks. The river arises at such an angle with
the lake that its source is almost invisible : it at once breaks
back at a right angle and flows south for a bit before winding
about in a westerly direction around the ends of the ranges
of hills. It has no falls or cascades, but runs swiftly, being
about as broad as the lower river at Oxford. The banks
are well marked, and not concealed by beds of papyrus.
I walked a mile or two along it, and was interested to see a
train leave Albertville for the interior. I also collected a
few insects, which I send you. [Among these were Sphex
(Parasphex) albisectus, Lep.; Bembex forcipata, Handl.;
Chromatophania fenestrata, Villen.; several specimens of
Pachytoma gigantea, Ulig.; and Cicindela intermedia, as on
the E. of the lake.]
‘We reached Albertville at about 9, and one’s first 1mpres-
sion was, * Why, this is Tropical Africa.’ It looked like the
old pictures and engravings one knows so well—and quite quite
different from the infernally dull bush country which seems
to compose most of late German East Africa, and also different
from, and more ‘tropical’ than, the Uganda shore of L.-
Victoria—partly, I think, because of the little steep tree-clad
hills, and sudden deep little valleys with ferns at the bottom;
and more palm trees than one is accustomed to see. We put
off again at 11 and went back to Toa to pick up the P.M.O.
It was a most lovely blue evening, full of colour, though no
more so than Victoria Nyanza. I! noted near the coast that
the water in places was quite green, in streaks, like the
patches of colour one sees in the Red Sea, except that the
(> cxivai >)
latter are red—both presumably due to Algae. We came
back to Albertville for the night, and slept on board, and I
had a delicious bathe next morning.
* On Jan. 7th we sailed along the coast southwards for
6 hours and returned to Albertville just after dark. As we
got more southward the mountains became higher, though
still forested, and their irregularity was interesting and
beautiful. Opposite us on the east coast, forming the most
marked prominence thereof, was a very fine rugged group
of mountains, named Kongue, rising to 5000 feet, which
through glasses appeared to descend sheer into the lake, and
one could see deep ravines and marks of waterfalls. I wished
we had been sailing along that side. At the end of our
6 hours’ run I got an hour ashore and secured a couple of
Coprids, both new to me, under cow droppings on the sand
[Liatongus planatus, Cast., 9, at Cape Tembwe; Sisyphus
crispatus, Gory, ¢, at Tembwe Bay]. We had a very pretty
pink sunset, and just after dark were met by a sudden
thunderstorm which nearly sank the boat we had been
towing, but it was secured alongside when the storm came
on. It was quite a savage little storm and very noisy, and
I was much interested, knowing so well the storms on Victoria !
‘“ Next day we returned to Toa, and sailed at 4 p.m. on
our way back to Kigoma. For 4 hours we plugged against
a heavy head wind and sea and got a good tossing—many
on board (including a real sailor, superintendent of the lake
ships) being sea-sick, but I much enjoyed the experience.
These storms on Tanganyika are much feared by the native.
canoemen, who never go far from land, but their dug-outs
are very poor sea boats compared to the fine built canoes on
L. Victoria.
** Now a few words about the differences between Victoria
Nyanza and Tanganyika. Except for the fact that both
contain fresh-water they are as different as they well could
be. But even in the water there is a difference, because of
the green areas of Tanganyika due tosome Alga. The coast-
line is very different—Victoria, comparatively ‘ tame-looking’
with low,.flat-topped hills, or marshes of papyrus—Tanganyika
with high steep mountains, ,and no marshes, and very very
(: cxlvitie)
little papyrus, altogether wilder-looking. Victoria is shallow :
I do not think its maximum depth reaches 600 feet, whereas
Tanganyika has been sounded to 6000 feet without touching
bottom. In shape, of course, they are very different, and
herein probably les the reason of the difference in depth.
Tanganyika fills up part of a great rift, whereas Victoria is
merely a huge rain-puddle. The well-known fauna of Tan-
ganyika is, of course, very different. I secured shells lke
Nassa, Trochus, Littorina, but some of the most peculiar
species have to be dredged for. Such fish as I saw being
sold were totally different from the ones I know in Victoria.
Curiously enough, during all the time I was on Tanganyika
I saw and heard no signs of the great fish eagle (I believe its
name is Haliaetus vociferans) which is so conspicuous on
Victoria, though I am told it exists on the lake. The flora
seemed very different—very few of the common bushes on
Victoria were noted on Tanganyika; and I saw many trees,
shrubs, and flowers new to me. I wished I had had time to
collect imsects on the forested hills of the western shore.
Some day I hope to return home by that route. From L,
Tanganyika to Boma, the ocean port at the mouth of the
Congo, I believe takes 20 days or so.”
Among the specimens captured at Kigoma on Jan. 9 were
a Fossor of the genus Trypoxylon near confrater, Kohl, and
the following Coleoptera—Ozxythyrea vitticollis, Boh., Lacco-
ptera turrigera, Boh., Aspidomorpha parummaculata, Boh., and
Mesoplatys ochroptera, Stal.
© Mar. 1, 1918.
“ T wrote to vou last from Dar es Salaam that I was just
off on a tour up-country again to tackle an outbreak of plague
in a district named Singidda, N. of the railway and 8.W. of
Arusha. I have just returned to the headquarters of the
Political Officer at the conclusion of the tour. Curiously
enough, I never saw a case. The epidemic appears to have
begun in mid-January, and there must have been about 100
deaths, but the people left the infected houses and bolted
into the bush, so that the outbreak was more or less stayed
(though I have “heard of three more deaths in the district
since I left it). I investigated about 112 deaths, of which
( cox 7)
83 had definite symptoms of plague, others doubtfully plague,
some probably anthrax. I have given about 750 inoculations,
but could only do * contacts,’ since the population is very
large and the vaccine very limited.
“It’s a most glorious country—the tail end of the Great
Rift Valley, with very lttle bush—nearly all a huge expanse
of undulating grass-land with a little bush in the hollows,
an escarpment each side (the valley being about 20 miles in
breadth) of about 300 feet, I suppose, with clumps of granite
rock cropping out along the top and here and there in the
valley. To the N.E. could always be seen a fine conical
peak rising, I suppose, about 3000 feet above the surrounding
country, called Amang (? why?) by the Germans, Neuruwe
by the natives of this part (Wanyaturu). It looks like a
volcano, and is marked on the map as being clothed with
primitive forest (ah-h-h!!!). But no chance of collecting
there! This is a very disappointing country for butterflies—
very few in species and individuals, but Synchloe is of interest,
as I haven't seen it since I caught it in the bottom of the
other rift (Kigezi!). But the paucity of butterflies is more
than compensated for by thousands of water and. wading
birds congregated on shallow lakes which dry up in the dry
season. Alas! I know so little about waders, but spotted
Avocets and Flamingoes! I watched one of the latter feed-
ing—he put his head under water in the well-known inverted
position, and then proceeded to circle round his own head,
which he kept under water until he had made two revolu-
tions, then put it down again in the same spot and circled
round it twice more, stepping sideways with trampling move-
ments of his feet. I suppose this trampling squeezed out of
the mud minute organisms which he strains out of the water
like a whale. I could spend hours with glasses (and oh, for
a cinema camera !). The birds are so tame you can sit down
and watch them within 20 yards! Flocks of Coots, so that
the water is black with them—which rather surprises me.
“ T expect to return to Dar es Salaam shortly, and then
get a month’s local leave, and then have asked—mainly for
Lepidopterous purposes!—to be sent to Portuguese East
Africa !”
(veclr=)
Caprain G. D. H. CaRPENTER’S PIERINES FROM LULANGUBU
AND Sr. Micuaru’s Misston.—Dr. F. A. Dixy exhibited
Capt. Carpenter's Pierines and made the following observa-
tions :—
The Pierines collected by Capt. G. D. H. Carpenter at
Lulanguru, seventeen miles W. of Tabora in East Africa, are
in several respects of great interest. The most noteworthy
captures are as follows :—
(1) A series of Teracolus ducissa, Dognin, consisting of five
males and seven females, including one pair taken i cop.
This pair settles the question of the male of 7. ducissa, which
has been erroneously stated to be like the female. In reality
it bears considerable resemblance to the male of TZ. sub-
fasciatus, Swains., from which it is chiefly distinguishable by
the fact of the dark subapical bar of the fore-wing being
continuous into the hind margin, and the included apical
eround-colour being of a deeper orange. Aurivillius in Seitz,
“ Macrolepidoptera of the Ethiopian Region,” p. 61, describes
the male of 7. ducissa as differmg only from the female by
its yellow ground-colour. His figures of the sexes (ibid.,
pl. 20, f, g) really represent two females; but the same plate
contains a figure of “* subfasciatus 2,” which may very well
have been drawn from the male of 7. ducissa. My attention
was called to this by Prof. Poulton.
(2) A long series of Teracolus casta, Gerst., comprising
twelve males and seventeen females; twelve of the total
number were taken paired. The males are mostly of the large
dark-bordered form called sipylus by Swinhoe. The females
show a remarkable range of variation.
The captures range in date from July 25, 1917, to Jan. 2, 1918.
Capt. Carpenter notes that the wet season began from the end of
November. In most of the species there is a well-marked corre-
spondence with the change in meteorological conditions. This
is evident in the case of the three species of Terias, T. brigitta,
Cram., regularis, Butl., and senegalensis, Boisd., though not
without some exceptions. The specimens of the first-named
species were caught July 25—Aug. 1, and are all of the dry-season
form, the males being somewhat transitional, and the females,
as is usual. having the dry-season character more strongly
(cli ~)
developed. The. 7. regularis caught in July are “ dry,”
though not markedly so; those captured from Nov. 23 to
Dec. 10 show a gradually increasing wet-season coloration.
July examples of T. hecabe are “dry”; a December male is
transitional, but a female captured on Dec. 31 is conspicuously
“dry.” On the other hand, a pair taken on Jan. | is “ wet ”’
in both sexes. In Teracolus regina, Trim., the dry-season
character is maintained in July. In December and January
it is replaced by the wet. Not much seasonal difference is
observable in Catopsilia florella, or in Teracolus ducissa; in
T. casta, however, the change is marked. The dry-season
character prevails throughout July; in October it begins to
yield; from November to the following January the wet-
season coloration is fully established. The specimens of
T. achine were taken in December; they are all of the full
wet-season phase. The same applies to the single example
of Teracolus annae, Wallgin. (caught in November). Two
July specimens of 7. eris, Klug, are “dry.” the remainder
(November and December) are ‘wet.’ Belenois severina
(July) is “dry.” Other forms of Belenois I reserve for
treatment on a future occasion.
Another consignment of Pierines from Capt. Carpenter
comes from St. Michael’s Mission, in Lat. 32° 45’ E., Long.
3° 45’ S. The earliest date for these specimens is Aug. 21,
the latest is Oct. 12. Capt. Carpenter notes, ‘ Dry season
till light rains in early October.”
The Teracolus callidia, T. oncretus, T. evagone and T. achine
were all taken in August, and in all the dry-season character
is well marked; as it is also in JT. evarne and T. annae
(October), Terias brigitta (Aug. and Sept.) and Belenots gidica
(Sept. and Oct.). The August and September Teracolus
rogersi are “dry,” the October specimen is “ wet.” All the
T. casta except one 9 were captured in August. The latter
(Oct. 8) shows an approach to the wet-season phase; the
remainder are all “dry.” It will be seen that in this series
of Pierines the correspondence of seasonal phases with Capt.
Carpenter’s note of seasonal conditions is remarkably close,
so far as the material goes. The “ light rains’ that began in
early October are immediately accompanied by a slight but
( clam)
distinct change in Teracolus rogersi and T. casta; in other
cases they have not, up to October 8, produced any perceptible
effect.
Nuptial Flight of Pierines.—It may be remembered that
in Proc. Ent. Soc. Lond., 1917, pp. lil, liv, a number of cases
were recorded in which paired specimens were taken by Capt.
Carpenter, the male in every instance but one supporting the
female. Since then many more pairs have been sent home
by Capt. Carpenter from the same locality (Itigi) as before ;
and in addition to these, further examples from Lulanguru.
The following is a list of all the Pierines actually captured in
the paired condition by Capt. Carpenter, including those
mentioned in the communication above referred to. It will
be understood that in every case the paired specimens them-
selves have been sent home by Capt. Carpenter, and may be
seen in the Hope Department.
Teracolus casita, Gerst. . . =. ~ . Ii pairs
P.evagore, Kigo: | 2S) an eee lapel
E-ducissa, Wook, i 4 eee al pale
Lachine; Cramoy ie «0. a sek Compas
Herpaema ervxphua, Godt. . . . . I pair
Pinacopteryx semana, Hopff. =... 35 pairs
Belenows gidica, Godt: . #3 2 =) Sl pair
B. mesentina, Cram. .. . . -. |.) . 10 pars
B. severina, Crams” . —-..) 4) >.) Sa BSE pats
Ternas reguiaris; Butle .) .\ 0) pane
T. senegalensis, Boisd. . . . . . I pair
Catcpsilia florella, Faby... . . . . 2 pairs
Kighty-one pairs in all.
Inasmuch as (except in one pair of P. simana) the female
was invariably supported by the male, it may, I think, be
concluded that this is the general rule in the subfamily
Pierinae.
Species or HeELIcoNiIus FROM FRENCH GuiAna.—Mr. W. J.
Kayek, on behalf of Mr. J. J. Jorcey, exhibited a very fine
series of named forms of Heliconius melpomene and its com-
panion species Heliconius erato from French Guiana. One or
two remarkable new forms of the former and a number of
( cliii_)
the form tellus of the latter were not present in a former
large collection from the same locality two years ago.
Monstrosity IN LEPTOTHORAX ACERVORUM, F.—Mr. Donis-
THORPE exhibited a very remarkable monstrosity of an ant,
which had been sent to him by Mr. R. Butterfield of Keighley,
who had taken it on April 26, 1918. in a mixed nest of Myrmica
ruginodis, Nyl, and Leptothorax acervorum, F., at Mauley Bog,
who suggested it might be a parasite. Mr. Donisthorpe
pointed out that it was a monstrosity of the Leptothorax,
being a small deilated 9, but unlike all the Myrmicine ants,
it only possessed one very small joint joining the epinotum
to the gaster, instead of a pedicel of two joints, the petiole
and. post-petiole.
He also exhibited a specimen of Elater sanguinolentus, Schr.,
taken on Wimbledon Common, May 28, 1918. He said that
when hunting for bees, etc., for Mr. Morice, he noticed this
beetle in some numbers, and as far as he was aware it had
not been taken on Wimbledon Common for twenty-five years.
ABERRATIONS OF British RHopALOCERA.—The Rev. G.
WHEELER exhibited a specimen of Pararge megaera, L., ab. 9
mediolugens, Fuchs, taken at Guildford on May 31st, and
observed that it was the first time he had met with this form
either in England or abroad. All the specimens of this
species met with on this day were unusually dark. He also
showed a fine specimen of the brassy aberration intermedia,
Tutt, of Rumicia phlaeas, L., taken at the same time and
place.
METHOD OF FORMATION OF * CUCKOO-SPIT,”” BY PHILAENUS
SPUMARIUS.—The PRESIDENT said that, as the nymph of
Philaenus spumarius—the common * cuckoo-spit”’ insect—was
now very abundant, and specimens for observation were easily
obtainable, he wished to call attention to a remarkable
peculiarity in its abdominal structure, which he had noticed
when examining the insect a few days ago, and to which he
could find no reference in any of the text-books or other works
he had had time to consult. The peculiarity consisted in
the fact that the tergites and pleurites of the abdomen from
the 3rd to the 9th, instead of ending as usual at the sides
to form lateral edges, are curved round and continued under-
( :cliv*)
neath the abdomen as membranous extensions, which meet
in a suture along the middle line, or sometimes even overlap
one another. Between them and the true ventral surface of
the abdomen a cavity is formed which is filled with air; and
it is into this air-chamber that the spiracles open. A median
triangular lobe arising from the sternite of the 2nd segment
fits in between the lobes of the 3rd segment, and together
with a ridge extending from it on each side, closes up the
air-chamber in front. Air can be admitted to, or expelled
from, the chamber by means of a Y-shaped slit or valve,
formed where the lobes of the 9th segment and the anal lobe
come together. Fabre in his account of the froth insect
(“ Souvenirs,” 7th Ser. 1900) had noticed this Y-shaped slit
at the end of the abdomen, and correctly observed that it
was by means of this valve that it blows its bubbles; but
this was about the only accurate observation in his account,
which for the rest must be treated as mainly conjectural or
imaginary. Kershaw, in a paper in “ Psyche ” for 1914, had
described the structure of the abdomen in the case of another
species of Cercopidae, but whether for the first time or not,
he was at present unable to say. Kershaw, however, main-
tained that the air which fills the bubbles was expelled along
with the liquid from the alimentary canal, thus upholding
the view which has been generally accepted since the time
of De Geer; and he believed that the chief function of the
air-chamber was to keep the spiracles from being clogged by
the froth which surrounds the insect. The President said he
was convinced from his own observations, confirmed by those
made by Mr. F. Muir at his invitation, that there was no air
mixed with the liquid as it issued from the anus; that the
air with which the bubbles of froth were blown was forced
out from the air-chamber beneath the abdomen through the
Y-shaped slit at its end. Glands at the sides of the 7th
and 8th abdominal segments from which tufts of white fila-
ments extend had been variously interpreted, Berlese con-
sidering them to be the source of the liquid secretion, and
Prof. Porta as a combination of wax-glands and tracheal
gills; but as he found that the white tufts were completely
dissolved in ether, he believed the glands were simply wax-
( ely.)
glands, though possibly they might secrete something of a
mucilaginous nature that gives coherence to the froth. He
hoped some of the Fellows present would take the oppor-
tunity to make observations on the insect with a view to
confirming or disproving the account he had just given.
[Since the date of this meeting, I have found that a full
account, agreeing in all essential respects with my own
observations, was given by Dr. Karel Sule in Zeit. fiir Wissen.
Zool. Bd. 99, pp. 147 et seg. (Nov. 1911).—C. J. G.]
Born Species or HeMARIS FROM THE New Forest.-—Mr.
Hamitton Druce exhibited about 30 specimens of Hemaris
tityus (bombyliformis) and H. fuciformis, which he had taken
near Brockenhurst on May 18th, 19th, 20th, and remarked
that the extensive wood cutting in the Forest had not
depleted their numbers.
Papers.
The following Papers were read :—
* Studies in Rhyncophora, iv; a preliminary note on the
Male Genitalia,” by Davip Suarp, M.A., M.B., F.R.S., ete.
“ Notes on the Ontogeny and Morphology of the Male
Genital Tube in Coleoptera,” by Freprerick Mutr, F.E.S.
* Notes on various Species of the American Genus Astylus,
Cast. (Coleoptera), with Descriptions of their Sexual Charac-
ters,” by G. C. Caampion, A.L.S., F.Z.S.
* New Staphylinidae from Singapore, pt. i1,’’ by Matcotm
Cameron, M.B., R.N.
Wednesday, October 2nd, 1918.
Dr. C. J. Ganan, M.A., D.Sc., President, in the Chair.
Alteration of Bye-law.
The proposed alteration in Bye-law vili was read for the
second time.
Exhibitions.
Lire-History or LycaENA ALcon.—Dr. CHapMAN exhibited
a bred specimen of Lycaena alcon, probably the first specimen
( clvi )
that has been bred, certainly the first from larvae taken in
the autumn, and made the following observations :—
The life-history is interesting as parallel to, but differing
from, that of Lycaena arion. The young larva feeds in the
autumn in the flowers and other portions of Gentiana pnewmo-
nanthe, and probably of other Gentians. So far it is exactly
parallel in growth to other Blues, such as many of our Plebeiids
that pass the winter in the third instar; when it reaches
the third instar it leaves the plant, wanders off, and, hitherto,
efforts to carry it further have failed. At this point it agrees
with Z. arion in habits, but it is not like LZ. arion, which is
in a remarkably modified and concentrated (as regards skin
armature) fourth instar, but is in quite an ordinary third
instar. In its plant life it has differed also in that several,
often five or six, larvae live amicably in one flower, whereas
L. arion is solitary, and if by any accident two larvae meet,
as by a second egg having been laid on the same flower-head,
or especially when incautiously associated in captivity, they
are inveterate cannibals.
The remaining history is that both arion and alcon live in
the nests of ants—I kept both species in those of Myrmica
scabrinodis—and pupate in the nest (re L. arion, teste Capt.
E. B. Purefoy). The differences are that L. arion eats the
ant brood, whereas L. alcon certainly sucks their juices
without eating them, and I could not prove that it ever
actually ate them, though I thought it did so when past the
winter, when its food would more often be ant pupae.
L. arion is in its fourth instar, and provided with a skin
armature not unsuitable to it when full grown. L. alcon has
only a third-instar armature, and when full grown might
almost be described as without one, for, like LZ. arion, it does
not moult after entering the ants’ nest, but attains its full
growth still in the third instar. The skin is then so attenuated
that the fat-masses are very obvious, and its general aspect
is like that of an internal feeder rather than that of a butterfly.
It is to be noted as exceedingly remarkable that a butterfly
larva should attain its full growth after only two moults.
Monsieur Oberthiir, who is familiar with localities where
L. alcon is common, and considered it highly probable that it
( clyu, )
had a history similar to that of Z. arion, and who with the
assistance of Mr. H. Powell found that ants would carry off
the larva of L. alcon, and that it would lap up the juices of
wounded ant larvae, provided me with the young larvae for
observation, in both 1916 and 1917, and my success in rearing
the insect is entirely due to his initiative.
My detailed notes have been sent to him to appear in the
“ Etudes de Lépidoptérologie comparée.”
Mr. Powell has seen the larva of LZ. alcon carried off by
Tetramorium caespitum and by Tapinoma erraticum. Acting
on this hint Mr. Donisthorpe provided himself with a nest of
Tetramorium, and now has a larva of L. alcon thriving in it.
T have larvae in nests of Myrmica scabrinodis and M. laevinodis.
AN OUTDOOR SPECIMEN OF THE CockroacH.—Mr, Donis-
THORPE exhibited a specimen of the common Cockroach
(Blatta orientalis) taken under bark of oak in the New Forest,
far away from any houses, July 29th, 1918. Dr. Neave and
the PRESIDENT commented on this exhibit.
ERGATANDROMORPH OF MyRMIca SuLCINODIS.—Mr. DonIs-
THORPE also exhibited a curious ergatandromorph of M.
sulcinodis taken on Bloxworth Heath, from the collection of
the late Rev. O. Pickard, Cambridge.
LaRVAL SKINS OF DyTIscus MARGINALIS.—Mr. HucH Main
exhibited the three larval skins of Dytiscus marginalis, pre-
pared for demonstration purposes. Ova were deposited in
captivity about the last week in May of this year. The
larvae hatched on June 4 and 5. The first moult of one of
the larvae took place on June 13, the second moult on June 28,
and the pupa was disclosed on July 28. The other larvae
passed through the same stages round about the same dates.
The empty larval skins were floated out and spread on glass
under water, and after drving were mounted up with a cover
glass like a lantern slide, strips of cardboard being inserted
to prevent pressure on the specimens.
EXPERIMENTS IN COLOUR-INHERITANCE IN PEDICULUS
HUMANUS.—Mr. Bacor, in referring to some breeding experi-
ments he had conducted respecting the inheritance of dark
and light coloration in Pediculus humanus, explained that
his results, which were of an indefinite character, were com-
( clviii_)
pletely valueless owing to the discovery by Sikora that these
insects reacted phototropically to the light or dark hue of
their surroundings. It appeared that the factors necessary
to the production of dark pigmentation were exposure in
some earlier instar to light while in a dark environment.
Individuals kept in complete darkness did not react. In his
experiments a strain of lice which showed only pale grevish
forms during the first three or four generations then com-
menced to produce dark (so-called melanic) individuals,
presumably owing to the white sides and grey flannel in the
box having been blackened with excrement by the insects
during this period. With regard to the lengthy series of
breeding experiments he had carried out the results curiously
simulated some features of discontinuous variation, suggesting
Mendelian inheritance in which the proportion of dark and
heht forms did not conform to theory. It appeared, in view
of Sikora’s discovery, that this was to be accounted for by
the chance exposure to light of susceptible larvae or nymphs
while amid dark surroundings during examination; the small
glass-bottomed boxes in which the broods were reared being
normally carried wrapped up in paper in a vest pocket,
where little, if any, light could penetrate. The nature of the
darkening was apparently twofold: (1) dependent upon the
pigmentation of the chitinised plates, and (2) to the suffusion
of the general skin surface. His own results suggested that,
while the first character might be present without the second,
the second was always accompanied by the first.
Paper.
The following paper was read, the author illustrating his
subject with photographs shown in the epidiascope.
“ Notes on Australian Sawflies, especially ‘ Authors’ Types ’
and the Specimens in the British Museum of Natural History
and the Hope Collection in the Oxford University Museum,
with Diagnostic Synopses of the Genera and Species,” by the
Rev. F. D. Moricr, M.A., F.E.S.
G@ ‘clic? )
Wednesday, October 16th, 1918.
Dr. 8. A. Neave, M.A., D.Sc., F.Z.8., Vice-President, in
the Chair.
Tea Fund.
The TREASURER having brought forward the question of
subscriptions to the Tea Fund, a discussion took place durmg
which the question was raised whether it would not be better
for the Society to provide tea as one of its regular expenses ;
a charge for tea was also suggested. Eventually it was agreed
nem. con., on the motion of Mr. EK. E. Green, seconded by
Mr. H. Rownanp-Brown, that the question be referred back
to the Council.
Alteration of Bye-law.
The proposed alteration in Bye-law viit was read for the
third time, and it was announced that the Special Meeting
would take place immediately before the Ordinary Meeting
on Nov. 6th, at 8 p.m.
A rare Coccrp.—Mr. KE. E. Green exhibited specimens of
a rare Coccid (Kermes quercus) taken on the stem of a single
oak, at Selby (Yorkshire). The species had been taken on
two or three occasions only, apparently in the London dis-
trict. The present examples were found to be associated
with dense groups of adventitious buds on the stems of the
tree, and were extraordinarily like the buds themselves.
KUPITHECIA HELVETICATA VAR. ARCEUTHATA AND A LIVING
Larva.—Mr. W. G. Saetpon exhibited specimens of Hupi-
thecia helveticata var. arceuthata, Frey, and a living larva from
Surrey, and made the following observations :—
E. helveticata, var. arceuthata has been known for many years
to occur locally in the south of England. It was discovered so
far back as 1862 by Harper Crewe, who in this and the following
year seems to have secured a number of larvae. Specimens
are said to have since been taken in Surrey, but the only
definite record seems to be one by B. A. Bower in E.M.M.,
vol. x. (2nd series) p, 42, who records two examples beaten
@ selx))
from Juniper from the neighbourhood of Croydon; the other
supposed specimens have turned out to be FE. satyrata (see
South * British Moths,” vol. ii, p. 239).
It seems to be exceedingly scarce in collections, the onlv
specimen purporting to be this form that I have seen is one
which was in the collection of the late C. A. Briggs, and
which I purchased at his sale; this is certainly not #. var.
arceuthata.
In 1915 a friend informed me he had beaten two green
Hupithecia larvae from Juniper in Surrey, and in the follow-
ing year bred two undoubted examples of this variety there-
from. In 1916, my friend having kindly given me the locality,
I obtained six larvae, from which I bred three examples. In
1917 thirteen larvae were obtained, from which, however,
only three more imagines resulted; whilst this year I could
only obtain four larvae.
It will thus be seen that H#. var. arceuthata seems rare, at
any rate in Surrey, and it is also exceedingly local, for all
my larvae have been obtained from one small group of Junipers,
although these shrubs are plentiful in the district.
Mr. Kaye and the Rev. F. D. Morice commented on this
exhibit.
New Sus-species oF HELiconius ERATO.—Mr. W. J. KAvE
exhibited a remarkable new form of Heliconius erato* for
which he proposed the name extrema. It formed a connecting
link between H. erato chestertoni and H. erato colombina. It
was remarked that both of these two occurred usually without
any but the most trivial variation. Both occurred in the
Cauca Valley of Colombia, over a great area from north to
south. In addition to the form extrema three others were
shown, which formed a graduating series to colombina; one
of these being very similar to extrema, but showing faintly
an indication of a transverse yellow band beneath, as well as
a very small indication of the fore-wing red band as found in
* Heliconius erato extrema, nov. Ss. sp.
Fore-wing dark bluish black with a steely gloss. Except for a
small red dot on the costa above discocellulars without markings.
Hind-wing like fore-wing unicolorous dark bluish black. No trace of
yellow transverse band either above or below. 1 6.
Hab. CotomsBtia, Cauca ( ?).
( clay)
colombina. These forms were purchased from a dealer with
only the information ** Colombia,” but it is almost certain
that they came from some part of the Cauca Valley. H. erato
molina fitted well into the connecting series, and had still more
red of the fore-wing band. It was recorded from Valdivia,
and was probably only an occasional aberration, as it was only
known from the type specimen.
Larva Skiys oF DyTISCUS MARGINALIS AND HYyDROPHILUS
piceus.—Mr. Hucu Main exhibited as transparencies in the
epidiascope the larval skins of Dytiscus marginalis, which had
been handed round at the meeting on Oct. 2. They appeared
quite satisfactorily on the screen, showing the general charac-
ters and such details as the manner of dehiscence of the skins
and the fringes of hairs on the various appendages, ete. It
was pointed out that the tail appendages in the first larval
skin were only fringed on the outer side, while in the succeed-
ing skins they were fringed on both sides. The moulted
skins of the larva of Hydrophilus piceus were also shown, and
the spread-out empty skin of the pupa.
Such series illustrated very graphically the great increase
in size of the larvae in the very limited time in which they
passed through this stage of their life-history, viz. just under
eight weeks from hatching of the ege to disclosure of the
pupa, in the case of both insects.
Mr. E. A. Butter commented on this exhrbit.
SPECIAL MEETING.
Wednesday, November 6th, 1918.
Dr. C. J. Ganan, M.A., D.Sc., President, in the Chair.
The Notice calling the Special Meeting was read by the
SECRETARY, the object of the meeting being to make an
alteration in Bye-law vill, the proposed change being sup-
ported by the TREASURER, the PRESIDENT, Comm. WALKER,
Dr. CHAPMAN, the Rev. F. D. Morice and Mr. Jongs.
The TREASURER formally proposed to delete Clause 5 of
Ch. viul, and to substitute :—
PROC. ENT. SOC. LOND., II, tv. 1918. L
( ‘claw )
“The Council shall nominate a chartered or incorporated
Accountant annually, who shall audit the Treasurer’s accounts.
The Auditor shall be paid for his services a fee, the amount
of which shall be agreed by the Council on behalf of the
Society. The Treasurer shall furnish the Accountant with ali
the facilities he may require for auditing the accounts.”
The Treasurer having fully explained his reasons for pro-
posing this alteration, it was seconded by Dr. Chapman and
carried nem. con.
ORDINARY MEETING.
Wednesday, November 6th, 1918.
Dr. C. J. Ganan, M.A., D.Sc., President, in the Chair.
Tea Arrangements.
The SecrETARY announced that the Tea question having
come before both the Business Committee and the Council,
the following recommendation had been agreed upon :—that
the tea subscription list should be circulated at every meeting
till the Annual Meeting inclusive, and that as soon as the
finances permit the tea should be provided at the expense of
the Society.
Election of Fellows.
The Rev. Fr. O’Nett, 8.J., Salisbury, Rhodesia; Messrs.
Ernest WitiraM Nimmy, 210 Whippendell Road, Watford,
Herts; R. Sranway Parris, 6 High Street, Bishop’s Stort-
ford; the Rev. Atrrep T. Stirr, Grantham, Victor Drive,
Leigh-on-Sea; Capt. WituiamM Henry Tapp, F.R.AS.,
F.R.G.S8., and Mrs. Eteanor Eva Tarp, of Loos, 88 Wickham
Way, Beckenham, Kent; and the Rev. E. Aprian Woop-
RUFFE-Peacock, F.L.S., F.G.S8., Cadney Vicarage, Brigg,
Lincolnshire, were elected Fellows of the Society.
( clxiii_ )
Lehibitions.
ORTHOPTERA FROM SALoNIcA.—-Mr. W. J. Lucas, exhibiting
some Orthoptera from Salonica, made the following observa-
tions :
From time to time Mr. P. J. Barraud, one of the Fellows
of this Society, has sent me insects from Salonica belonging
to the orders Orthoptera, Odonata, and Neuroptera. This
evening I have brought up the Orthoptera, mainly for the
sake of a very interesting form of the common earwig Forficula
auricularia, Linn. They comprise :—
Lalidura riparia, Pall.—One male from Salt Lake near
Naresh, Salonica-Janes Road, Aug. 4, 1918. It is scarcely
as large as some of our south-coast examples and much darker
in colour, unless this is due to change in drying.
Forficula auricularia, Linn. var.—Six males and_ three
females. There is a large whitish spot on the wing-tips
(sometimes indicated in British specimens); the colour is
dark; and all the males sent have “high” callipers, the
greatest length in a straight line from base to tip being 9 mm.
It was common, or fairly so, in May and June 1917 and 1918,
at Sarach (1000 ft.) and Paprat (2200 ft.).. It was also found
(females apparently) in winter at Basanli, hibernating in a
rotten cherry log.
Empusa fasciata, Brullé.-—A male, taken June 4, 1917, at
Saracli.
Gryllotalpa gryllotalpa, Linn.—A female, from Kopriva,
Struma Valley, Salonica. It was common at low elevations
in April, May and June 1918.
MacEDONIAN OrtTHoPTERA.—Captain Burr exhibited a
series of Orthoptera from Macedonia, including Saga natoliae,
S. viltata, and Saga sp.n.; also a pair of Dinarchus dasypus,
Illig., and a small series of Glyphanus heldreichi, Br., a
wingless Qidipodid, which assimilates very closely to the
eround, but on jumping turns a somersault which flashes its
white ventral surface; the mner face of the posterior femora
are bright blue and lemon yellow, and the neck membrane
bright indigo, but none of these brilliant colours are exposed
under ordinary circumstances. It has been suggested that
( clxiv )
they may serve as signals between individuals, as the creature
is apparently mute. Also a small Caloptenus italicus, L., 3,
together with a Sphingonotus caerulans, L., 2, which were
taken in copuld.
Mr. Rowianp-Brown inquired whether the Macedonian
insects of other orders than Lepidoptera were predominantly
Western. He had been struck by this characteristic of the
butterflies sent to him from Salonica. Capt. Burr replied
that this was so, and that the fauna of the northern Balkans
was much richer than that of Macedonia, especially in the
plains. He added that one rarely saw a bird either that one
might not as well have met with in England.
CHALCID IN UNDIGESTED SEED.—The PrestDENT exhibited
a Chaleid, Torymus elegans, Borkh., sent to him by the Rev.
E. A. Woodruffe- Peacock, which had emerged from a hawthorn
seed which had passed through the alimentary canal of a
blackbird, together with the seed from which it had emerged.
He said that it had been parasitic on some insect, probably
a Cecidomyid, which had been feeding in the seed.
Mr. GREEN asked whether there were not Chalcids that fed
directly upon seeds, and the President replied that this was
the case, but that this species was parasitic.
Dr. NEAVE remarked that there were Chalcids that fed
within the stones of almonds and plums.
BUTTERFLIES OF THE GENUS CASTNIA AND A MIMETIC
Hesprerip.—Mr. L. B. Prout, on behalf of Mr. J. J. Jorcry;
exhibited the followimg species :—
Castnia erycina, Westw. (P.Z.8., 1881, p. 141, pl. xu, fig. 4),
paratypes out of the Druce collection, together with an
apparently very rare Erycinid butterfly (genus Xenandria *)
erroneously described by Druce as ** Castnia” pelopia (K.M.M.
xxvi, p. 69). Druce was evidently misled by the marvellous
resemblance between these two, and did not examine the
structure. A careful discussion of these forms by Houlbert
(Oberth., “ Et. Lép.” xv, pp. 654-8) is in part stultified by
the fact that Westwood’s figure is unrecognisable, showing a
red band which is really wanting, im consequence of which
he has thought to have discovered a new species peloprordes,
which will really sink to erycina; in part also by Druce’s
(ee claay =)
error above referred to. Although erycina is only definitely
known from the Sarayacu district, while the only known
examples of pelopia are from “interior of Colombia” and
Chanchamayo (E. Peru), one cannot doubt that they will
prove to occupy the same ground and to share in some mimetic
association,
Also several new or doubtful forms of Castnia, not yet
fully worked out.
FuRTHER OBSERVATIONS ON THE * CucKkoo-spit ”’ INSECT.—
The PRESIDENT stated that since the meeting on June 5th,
when he gave a short account of his observations on the
‘ cuckoo-spit ” insect, he found that an elaborate and very
interesting paper on the same subject had been published by
Dr. Karel Sule in November 1911. It was some satisfaction
to him to know that while his own main observations turned
out not to be new, they were almost in complete accord with
those of the Bohemian entomologist. There was one fact,
however, frequently observed by himself which seemed to
have escaped the observation of Dr. Sule and other writers
on the subject. According to them, the liquid excreted from
the anus accumulates beneath the body of the insect; and
into this liquid the tip of the abdomen is dipped, and then
the bubbles of froth are blown. But when the insect has
moved away into a new position, bubbles are generally pro-
duced before there is sufficient liquid under the insect in which
to dip the end of its body. What he saw happen on such
occasions was this: the insect at first stretches out its
abdomen, directing it obliquely upwards, and the lips of the
valve which admits air to the ventral air-chamber are at this
time kept open; this condition lasts awhile, and then the
liquid coming from the anus forms a film across the open
valve, the abdomen is now dipped downwards and a little
to one side, and at the same time the lips of the valve gradually
close, and the bubble, which during the process has been
forming, is set free; the tip of the abdomen is again raised,
and then dipped down towards the other side. In this way
the bubbles are formed and deposited alternately right and
left of the insect, and gradually are pressed forwards along
each side. He believed that it was the mere pressure exerted
( “eleva, >
by the bending down of the abdomen which forced the air
from the air-chamber into each bubble. A consideration of
the exact method by which the bubbles are formed was not
without importance in relation to the question of what part,
if any, the secretion of the wax-glands takes in giving to the
liquid secretion from the anus its capacity for forming bubbles.
Dr. Sule explains that the wax is acted upon by an enzyme
in the alimentary secretion, and the acid thus produced forms,
with the alkali present, a substance which gives to the liquid
the properties of a soap-solution. Although he had himself
at first suspected that the wax might in some way impart
to the liquid its tendency to form lasting bubbles, he was
on the whole inclined to doubt whether that did actually
take place.
As further points of interest in connection with the frog-
hoppers, he stated (1) that the median triangular lobe which
in the nymph fits in between the lateral folds of the 3rd
abdominal segment and helps to close up the air-chamber in
front, persists in the imago of many of the species, where it
is no longer functional, and takes the form of a median ridge
continued behind into a short, pointed process; and (2) that
when examining some nymphs alive under the microscope,
he found pulsatile organs, of the kind described in Nepidae
and some other water-bugs, present in the tibiae of all the
legs, and the movement of the blood corpuscles in the legs
very distinctly visible. Organs of the same kind had quite
recently been discovered by Richardson in the Aphididae,
and probably occurred generally in the Rhynchota and _pos-
sibly also in other insects. He thought it might be of interest
also to mention that the froth produced by the frog-hopper
was in the days of Queen Elizabeth known as “ Woodseare,”’
and he would like to find out whether that name has survived
anywhere in the British Islands up to the present time. Bacon,
in referring to the froth, said of it: “* The experience is that
the froth which they call Woodsare (being like a kind of
spittle is found but upon certain herbs, and those hot ones;
as lavender, sage, hyssope, &c. Of the cause of this enquire
further, for it seemeth to be a secret.” In a work published
in 1664 it is referred to thus: “* That spumeous froth or dew
( clxvii )
which here in the North we call Cuckoo-spittle and in the
South, Woodsear.”’ Possibly some persons might be influenced
in their choice between these two names if they knew what
the old English entomologist Moufet, who died in 1604, had
to say on the subject: “* Angli spumeam illam materiam
Wood-seare vocant; quasi diceres, silvarum tabem: Germani
cuculi salivam esse autumant.” Moufet was familiar with
the insect which comes from the “ Cuckoo-spit,”’ and said he
had no hesitation in calling it a little grasshopper (* Locust-
ella’’) rather than a Cicada, as Isidore, Bishop of Seville,
had stated it to be. Isidore, however, was not far wrong;
and John Ray came still nearer to the truth when he named
it “ Cicadula,’’
4
Death of a Fellow.
Prof. PouLtron said he was sure the Society would regret
to hear that Mr. C. W. FarquHarson, who had done so
much valuable work in Africa, had been drowned in the
sinking of the Burutw when on his way home on leave.
Paper.
The following paper was read :—
“Notes on a large Heliconine Collection made in French
Guiana in 1917, compared with a similar Collection made in
1915,” by J. J. Joicey, F.E.S., and W. J. Kayvz, F.E.S.
Wednesday, November 20th, 1918.
Dr. C. J. Ganan, M.A., D.Sc., President, in the Chair.
Election of a Fellow.
Mr. JosepH Herrop-Hempsatt, Orchard House, Stocking-
stone Road, Round Green, Luton, Beds., was elected a Fellow
of the Society.
Nomination of Officers and Council.
The following list of Fellows nominated by the Council to
hold office durme the ensuing year was read :—
( elxvi. 4)
President, Comm. JAMES J. WALKER, M.A., R.N., F.LS.
Treasurer, W. G. Sueupon. Secretaries, Rev. GErorGE
WHEELER, M.A., F.Z.8.; Dr. S. A. Neave, M.A., D.Sc., F.Z.8.
Tnbrarian, GEORGE CHARLES Cuampton, F.Z.8., A.L.8S. Other
Members of Council, EK. C. Bepweti; G. T. Betoune-BaKer,
F.L.S., F.Z.8.; Kennetu G. Buatr, B.Sc.; Maucotm CAMERON,
M.B., R.N.; W. C. Crawiey, B.A.; J. Hartuey Durrant;
Dr. H. Exrrincuam, M.A., D.Sc., F.Z.S.; Dr. C. J. -Ganan,
M.A., D.Se.; Dr. A. D. Is, M.A., D.Sc., F.L.S.; Dr. G. A. K.
MarsHaL, D.Sc., F.Z.8.; Rev. F. D. Morice, M.A., F.ZS.;
HERBERT Ji. Pace.
Eahibitions.
A NEW FORM OF MorpHo EUGENIA.—Mr. ArtTHUR DICKSEE
exhibited three specimens of a new race of Morpho eugenia
from Colombia, from which it was hitherto unknown, together
with two Morpho eugenia from French Guiana, and one
Morpho adonis from French Guiana, and another from the
Lower Amazons, for comparison.
He pointed out that the shape was half-way between the
rounded form of evgenia and the pomted form of adonis, and
that the colour approached more nearly to the colour of
adonis, whereas the white costal markings approached more
nearly to M. eugenia. He gave it the name of Morpho
eugenia, form damocles. The locality is Villavicencio, Colombia,
and the dates are May and June 1918.
Mr. W. J. Kayr commented on this exhibit.
Brep LycaENA ARION.—-Capt. PUREFOoY exhibited a score
of home-bred L. avion, together with their pupa cases.
He pointed out that the full-fed larva seldom, if ever,
attempted to crawl far away from the ants in order to pupate.
Larvae which he had kept both in the nests of IZ. scabrinodis
and M. laevinodis generally fed in chambers deep down in
the nest where the small ant larvae in their last instar were
cared for by the workers. When the arion larva was full fed
he generally remained where he was among the brood, slowly
changing colour from a fine ochreous hue to a dead grey
white. Six or seven days might elapse before the larval skin
was cast. The ants were running over their guest all the
time but never attacked him, even when the fresh pupa was
( ‘elax )
at its softest. The cremastral hooks would finally lose their
hold of the silk pad and the pupa would lie at the bottom
of the little earth chamber. When, after twenty-four days
or so, the imago emerged, it had to find its way to the surface
through the ant passages. This it never failed to do, and
the freshly emerged butterfly would be found during the
early morning drying its wings on the herbage growing on
the nest.
Dr. CHAPMAN observed that when ants were placed in a
new nest they refused to accept a larva of L. alcon, although
they willmely accepted that of L. arion.
DARKENING OF HIND-WING IN MECHANITIS POLYMNIA.—Mr.
W. J. Kaye exhibited six female Mechanitis polymnia from
the Berbice River, caught at Friendship in July 1914 by
Mr. H.C. Patoir, which all showed a very considerable darken-
ing of the outer half of the hind-wing, one in particular having
the whole outer half black. Two female MW. polymnia were
also shown from the Potaro River, in Central British Guiana,
which were the blackest that had been taken, one of which
was figured in the Trans. Ent. Soc., pl. xxiii, fig. 3, 1906. — It
certainly appeared as if towards Surinam the darkening in
this species was more pronounced, and probably it would be
found the same in the whole mimetic group of which JM,
polymnia was a member,
Paper.
The following paper was read :—
“The Hymenoptera of Fiji,” by RowLanp E. TuRNER,
FES.
Wednesday, December 4th, 1918.
Dr. C. J. Ganan, M.A., D.Sc., President, in the Chair.
Nominations for Officers and Council.
No alternative names having been received, the list of the
Council’s nominees for office for the ensuing year was again
read,
( velxx —)
Election of Fellows.
Messrs. ANDERSON FeERGussoN, 22 Polworth Gardens,
Glasgow, W.; GeorGe Grace, B.Sc., A.R.C.Sc., Inglenook,
Utley, Keighley, Yorks, and P. V. Isaacs, B.A., Assistant
Entomologist to the Madras Agricultural College and Research
Institute, Coimbatore, India, were elected Fellows of the
Society.
Exhibitions.
NEUROPTERA FROM SaLonica.—Mr. W. J. Lucas exhibited
the following Neuroptera from Salonica, sent to him by Mr,
P. J. Barraud in 1916-1918, viz.:—
Nemoptera sinuata, Oliv., three; Formicaleo tetragrammicus,
Fabr., one; Myrmecaelurus trigrammus, Pall, one; Palpares
libelluloides, Linn., two, a male and a female; Osmylus
chrysops, Linn., two; Ascalaphus macaronius, Scop., var.
kolyvanensis, Laxm., one male.
THE MALES OF GLUTOPHRISSA EPAPHIA AND PHRISSURA
SABINA DISTINGUISHED BY THEIR SCENT-SCALES.—Dr, F. A.
Dixey exhibited specimens of the males and females of
G. epaphia and P. sabina, with outline drawings of their
scent-scales. He said :—
Among the Piermes which may be comprehensively ranked
under the genus Appias, as now in the British Museum, there
are two African forms which appeared in that collection until
lately as Glutophrissa epaphia, Cram., and Phrissura sabina,
Feld. The females of both these forms do not resemble their
respective males, and also differ widely from each other; but
the males, though generally dist:nguishable without much
difficulty, are sometimes so much alike as to render their
determination by ordinary methods doubtful. Aurivillius in
Seitz’s ‘‘ Macrolepidoptera, Ethiopian Region,” Eng. ed., p. 38,
says of G. epaphia: “* The 3 nearly approaches that of sabina,
but is smaller and the black dot at the end of vein 1 on the
fore-wing above is always wanting.” These, however, are
not invariable means of distinction, for some individuals of
epaphia are larger than some of sabina, and the black dot at
the end of vein 1 may be wanting in the latter, especially in
the form inhabiting Madagascar. I think, however, that the
(else; 7)
males can always be distinguished by the shape of their
scent-scales; the females, as above noticed, present no
difficulty.
The scent-scales show some individual differences, but the
laminae of those of G. epaphia appear always to have parallel
sides, with a somewhat squared base and a comparatively
shallow apex. In P. sabina the sides may be parallel or may
be curved towards each other like a pair of parenthesis-marks,
but the base is always rounded and the apex comparatively
sharp. When the sides are parallel, the lamina of P. sabina
may be called U-shaped; when they are curved, the lamina
tends to become cordate. In either case it differs from the
almost rectangular proximal portion of the lamina in @,
epaphia. This distinction holds good not only for the con-
tinental forms of the two species, but also for their respective
forms found in Madagascar.
It may here be worth while to point out that a certain
amount of confusion exists with regard to the Madagascar
form of P. sabina. The female of this subspecies was originally
described and figured by Boisduval as. Pieris phileris, 9
(“ Faun. Lép. de Madag.,” p. 17, pl. 2, fig. 5). It does not,
however, belong to the male Pieris (Belenois) phileris with
which Boisduval associated it; and this author’s name for it
will therefore not stand. In 1872 it was included by Mr.
Butler in his list of species of the old genus Pieris as Belenots
confusa sp.n. Butler afterwards described a similar female
as Belenois coniata 3 (* Cist. Entom.” 2, p. 391). Mabille
(° Hist. Nat. de Madag., Léepid.,” i, p. 263, pl. 34, figs. 5,
5a, 6, 6A) described and figured the form under Butler’s name
of Pieris confusa. His descriptions and figures of the ** male ”
and female are, however, in every case those of the latter
sex. These mistakes no doubt arose from the fact that in
these two species, as in several other forms of the Appias
group, the female as well as the male is furnished with a
terminal tuft of hairs, quite distinct, though smaller than
that of the males. This fact, together with the great diversity
between the appearance of the sexes in P. sabina or confusa,
and the ease with which the males of that species may be
taken for those of G. epaphia, has led to the very natural
( clam” ))
though erroneous conclusion that both sexes of P. confusa
were represented in a series which consisted only of females.
It seems probable that the male of P. confusa was really
known to Mabille, but was not distinguished by him from
the male of G. epaphia; for his figures of ** P. saba typiea, 3,”
and “ P. saba var. epaphia, 3, might quite well be taken to
represent males of P. confusa (op. cit., pl. 36, figs. 3, 3a,
DA)!
THE RELATION OF THE ANAL TUFTS TO THE BRANDS OF
THE HIND-WINGS OBSERVED AND THE SCENT PERCEIVED IN A
MALE DANAINE BUTTERFLY BY W. A. LamsBorn.—Prof.
PouLToNn gave an account of the following deeply interesting
observations made at Tanga, late German Hast Africa, on
Aug. 5, 1918, by Mr. W. A. Lamborn, in continuation of his
S. Nigerian investigations, recorded in Proc. Ent. Soc. Lond.,
1911, xlvi; 1912, xxxiv; 1913, Ixxxiii, and those of Capt.
Carpenter, zbid., 1914, exi: .
“ Aug. 5, 1918.—To-day, a Bank Holiday, and kept as
such even in Tanga, afforded me relief from the care of my
usual 60 or 70 out-patients, and, the day being wet and dull
at intervals, I was able to sit in my office, getting the hospital
books m order, untroubled by any special hankering after
the things of the bush. Then, after an early lunch, I saun-
tered out, at 1 p.m., to make further search for Fleurya or
some plant near it; for all my recent rambles have been
devoted to this object. At about two the sun suddenly came
out brilliantly, arousing the insects; and the abundant
Amauris niavius dominicanus, Trimen, in particular claimed
my attention, for even now, as in Nigeria, I still often con-
fuse, for the few vital seconds, till they get to a distance, or
unless they settle, Amauris and Euralia. The majority of
the Amauris came to rest after a short flight and sunned
themselves, resting with wings approximated and then fully
expanded, evidently enjoying the warmth. Suddenly my
attention was attracted to a fine fresh male resting with
expanded wings by the gleam in the sunshine of a white
structure at the hinder end of its body. On near approach
I discovered that this was due to the extrusion of the anal
tufts, the gleam being due to the sunshine reflected off a
(Velxxn1 %)
pencil of brownish white hairs resting on the inner side of
the scent-patches. The outer black hairs were spread out
fanwise, accurately covering the patch, the foremost hairs
pointing towards the head of the insect, the middle hairs at
right angles to the mid-line of the body, and the hindmost
hairs pointing directly back. The abdomen of the insect at
the junction of the 10th and 11th segments was strongly ante-
flexed, the 9th and 10th segments being tumid, the 11th and
12th markedly constricted, an effect due, I thought, probably
to the strong tonic action of a detrusor muscle concerned
with the anal tufts. The butterfly remained motionless for
some seconds in this attitude, and then regular but sudden
movements of the wings took place, the fore-wings being
approximated and then over-extended, the hind-wings follow-
ing to about half-approximation and then also being over-
extended. By this means a slight movement of the black
hairs over the scent-patches only was effected. The operation
took place 10 or 12 times in half as many seconds, and then,
the tufts being withdrawn, the butterfly leisurely approximated
its wings and flew away.
“T found that almost as many males as I followed, old
worn specimens as well as fresh ones, eventually settled and
performed the same operation, which I studied in several
more. One, an old damaged insect, which had settled on a
leaf, extruded its mght white tuft, but could not at first
manage to get out the left. I could see peristaltic waves of
contraction passing down the last three segments of its ante-
flexed abdomen, for half a minute to no purpose. The violent
expulsive efforts then resulted in the extrusion of the two
tufts, but even then it was only able to spread the black hairs
of the left tuft over the corresponding patch. The brownish
white tuft did not appear. The subsequent movements were
as in the fitst-mentioned butterfly. It flew away after a
time and again endeavoured to exsert the paler tuft, but
unsuccessfully.
“1 then followed a second male and timed the operation
by the second-hand of my watch. From the first extrusion
of the tufts to their complete retraction lasted 1 minute,
40 seconds. These butterflies were so intent on their toilet
( *clsxive 3)
that I was able to approach my nose to within two or three
inches of a third with tufts extruded. I experienced a sensa-
tion as if an aromatic snuff had impinged on the mucous
membrane of my nostrils. Subsequently I seized by one wing
a fourth butterfly with tufts extruded. They remained ex-
truded in spite of its struggles, and on smelling them I
experienced the same sensation.”
The movements described in this valuable record strongly
supported Dr. H. Eltrmgham’s interpretation, in Trans. Ent.
Soc. Lond., 1915, p. 404, based on an examination of the
structures in the laboratory :—
‘““ We may suppose that the insect brushes out the secretion,
the stiffer [darker] hairs probably assisting im lifting the
covering scales. . . . It should be noted that these hairs are
on the outer side of the brush, and would thus naturally
come first into contact with the scent-patch.”
Dr. Eltringham’s researches showed that there was no
special muscle directly concerned with the protrusion of the
brushes. This was effected, as in many similarly eversible
glandular and odoriferous structures, by the pressure of the
fluids of the body. The constricted 11th and 12th segments
and the peristaltic waves of contraction described by Mr.
Lamborn were doubtless instrumental in producing this
pressure.
A SUGGESTED INTERPRETATION OF THE SPECIAL ATTACKS
MADE BY BLOOD-SUCKING DIPTERA ON NEW-COMERS INTO THE
TROPICS AND OF THEIR GRADUAL DIMINUTION.—Prof. POULTON
said that he had received the following suggestive notes from
Mr. C. B. Willams, who had written from the Department
of Agriculture, Trinidad, B.W.I., on Oct. 12, 1918 :—
*T got last mail Parts II, II] and IV of the Trans. Ent.
Soc. for 1917 (somewhat delayed !), and was particularly
interested in a discussion (pp. 1xxvii ef seq.) on the attraction
of insects to salts, perspiration, urine, etc., because it largely
fits in with some of my own ideas and observations on the
subject. Ihave ventured a little further, and have developed
a theory which appears to me to be sound. It is that relative
resistance to mosquito bites 1s due to differences in the com-
position, and hence the scent, of the perspiration, and further
(@ clxxws)
that after residing for some time in a hot climate the relative
proportions of various waste products secreted internally and
externally alter. The composition of the perspiration alters
and the individual becomes less attractive to mosquitoes than
when newly arrived. In spite of the fact that new-comers
perspire more freely than natives, who take things more
gently, I believe that mosquitces are not attracted by such
differences in quantity but in the quality of the secretion. I
admit nine-tenths of this is conjecture, but it is the only
working hypothesis that I can get that will explain the facts.
I have tested it for two years now. There seems to be no
doubt whatever that a new arrival to the tropics is more
worried and more bitten by mosquitoes. It is not a matter
of suffering more from the bites. I still swell and suffer from
any bite, but there are places where I can now sit in comfort
where I was continually bitten on my first arrival; and I
find that new-comers still suffer when sitting alongside me at
these same places, so that there has been no reduction in
the number of mosquitoes.
* Of course I know that the mosquito goes to get blood
and not perspiration as in the case of the butterflies discussed
in the P.E.S., but still it must be the scent of the perspira-
tion that originally attracts them to their prey. Tabanids
are blood-suckers, yet I have seen them attracted to a pair
of socks just removed after a hot walk.
* T wonder if some Bio-Chemist could be persuaded to take
up the study of the composition of perspiration in relation to
climate and mosquito attraction. It seems to me that it
might lead to the discovery of some attractive baits for
mosquitoes and possibly even for tsetse flies, to which the
reasoning might also apply.
“ T was particularly pleased with the remark in the Pro-
ceedings about gout accounting for the non-attraction of
butterflies to the perspiration of one individual. I believe
gout is due to faulty kidney action, and this would of necessity
have a direct effect on the composition of the perspiration.
* T should be very glad if vou would let me know what
you think of this idea. Quite possibly it has been proposed
before, but if so I have not heard of it. If you think it of
( elxxvi
) %
sufficient interest you might perhaps put it before the Entomo-
logical Society, to be pulled to pieces by more experienced
hands.”
Prof. Poulton said that the hypothesis was quite new to
him, and that he thought it was important to put it on record
as soon as possible, so that Entomologists generally might
test it by past experience and future specially directed
observation.
Mr. Bacor said that experiments carried out in West Africa
with Stegyomyia supported Mr. Willams’ theory; Mr. E. EH.
GREEN had found that during the whole of his residence in
Ceylon he remained equally affected by the bites of mosquitoes,
but that in England, though much attacked. he suffered no
inconvenience from them. Mr. H. Dotuman and the Rev. G.
WHEELER gave evidence from personal experience from resi-
dence in Central South Africa and Switzerland respectively,
supporting the view that partial or even complete immunity
was acquired after a time, and Mr. Bacor added evidence
that this immunity lasts for many years. Dr. LoNGsTAFF
and Mr. BerHune-Baker also adduced similar evidence with
regard to the stings of bees and wasps. Mr. MaLcoLm CAMERON
pointed out that the personal element had also to be con-
sidered, insects attacking some people much more readily and
persistently than others.
RHOPALOCERA FROM SouTH CENTRAL Arrica.—Mr. H.
DotimMaN exhibited two series of some thirty specimens each
of bred Charaxes: they represented two distinct species of
the ‘‘ etheocles’ group, the one having the 2 form of manica,
Trim. (resembling small 2° bohemanni), the other having the
2 form of phaeus, Hew. (resembling small 3 bohemanni).
It was pointed out that there were constant and readily
seen differentia in the respective males, and that in the great
number of females bred the latter had never departed from
the forms exhibited. The phagus form having been bred in
every month of the year, and the manica form, though not so
extensively, but throughout several months (ine asive of the
extreme wet and extreme dry periods), it may perhaps be
concluded that there is no marked seasonal instability of
either sex of the two species in this locality. The respective
( clxxvii_ )
larvae, drawings of which were shown, are quite distinct,
both superficially and structurally. They feed on different
leguminous trees—the manica form on an “acacia” called
in Chikaonde “ musasi,” the phaeus form on an ‘
called ** habulwebulwe.”
The pupae also show distinctive characters; these are smal]
but quite constant.
The experiments were conducted at Soltvezi, Kasempa
District, in South Central Africa, close to the Katanga bound-
ary. The phaeus form had not been observed further south,
but manica had been taken sparingly near to Broken Hill and
Kashitu.
The exhibitor expressed the opinion that the two species
were undoubtedly distinct.
_ He also exhibited a drawer of Nymphaline butterflies and
details of their life-history. The first two species were Hama-
numida daedulus, Fabr., and Crenidomimas concordia, Hopft.,
their pupae, and drawings of their larvae. The larva of
Crenidomimas, previously unknown, was shown to be exceed-
ingly similar to the well-known Hamanumida; their food-
plants are different. Dvrestogyna iris, Auriv., was mentioned
as having the same type of larva, of which, unfortunately,
no drawing had been made. It feeds upon the big-leaved
“musuku” tree. In the same exhibit was a bred series of
Pseudacraea pogger, Dewitz, its pupae, and figures of the
larva. Previously undescribed, the larva and pupa are of
interest as showing such very close resemblance to the con-
generic species. The larvae, though found in some numbers,
are restricted to one kind of shrub—*‘tandakatali”’ (Chikaonde).
The pupae are very freely parasitised by a small Tachinid fly.
All the material of the second exhibit was from South Central
Africa—either N.W. Rhodesia or the Katanga.
Prof. Poutron and Lord RoruscHILp commented on this
exhibit.
A LOCAL RACE OF Precis ocravia.—Lord Rorascurmp
exhibited a series of a local race of Precis octavia from Tembora,
* acacia ”
Bahr-el-Gazal, and drew attention to the extraordinary number
of intermediate specimens among the series of the dry-se ison
form—14 out of 16. He also exhibited a series of wet- and
PROU, ENT. SOC, LOND., V. 1918. M
( clxxviii_ )
dry-season forms with intermediates of Precis octavia octavia,
Cram., and Precis octavia sesamus, Trimen, from West and
South Africa respectively, for comparison. He also remarked
on a series from the Nuba Hills, Soudan, exhibited by Prof.
Poulton, and pointed out that, contrary to the Tembora
series, the dry-season forms were all pure dry-season, no inter-
mediates being present. The wet-season form appears also
to be paler. *
Dr. G. A. K. Marsuatt said that he had bred many inter-
mediates under abnormal conditions, and that any kind of
shock seemed efficacious in bringing about this result.
Lord Roruscuitp said that in experiments on Aglais
urticae he had found that it was only during a very short
period just before hardening that the pupa was susceptible
to surrounding influences.
Paper.
The following paper was read :—
“ Butterfly Vision,’ by H. E:rrrncuam, M.A., D.Sc., F.Z.S.
The paper was illustrated by means of lantern slides showing
the structure and optical action of the butterfly eye, and the
author also described and illustrated a series of experiments
designed to test the capacity of butterflies for perceiving
colours. He had arrived at the conclusion that the optical
image provided for the perception of the insect’s brain was
at least eight times more distinct than had been supposed
under previous theories, and also that though the butterflies
with which he had experimented were in some cases rather
“ short’ at the red end of the spectrum, there was strong
evidence that they could distinguish at least those colours
with which they were associated in life.
Dr. Lonestarr warmly complimented the author on his
paper and recalled one of his own observations in Jamaica
where a yellow butterfly had selected and settled upon a yellow
leaf lying on a wide area of uniform green. Dr. Eltringham
had mentioned a very remarkable fact in connection with the
actinic properties of the yellow flowers of the Rudbeckia, and
he had himself observed the overwhelmingly brilliant effect of
( clxxix )
this flower growing near Quebec against a dark backercund
of leaves.
Mr. Bacor recalled the theory that the colours of flowers
had been developed in response to the tastes of insects.
Dr. Dixry, Mr. BerHUNE-BaAkER and others also contributed
to the discussion.
Dr. Eltringham in reply said that he had been able to give
only an abstract of his paper, and that the points raised would
be found more fully discussed in the complete publication.
( clxxx )
THE ANNUAL MEETING.
The Annual Meeting took place on Wednesday, January 15th,
1919, Dr. C. J. Ganan, M.A., D.Sc., President, being in the
Chair.
The TREASURER, after explaining the position of affairs
under the new bye-law governing the audit, read his State-
ment of Accounts, which was adopted on the motion of
Mr. W. J. Lucas, seconded by Mr. HucH Mary.
The Rev. G. WHEELER, one of the Secretaries, then read
the following
Report of the Council.
Adverse circumstances notwithstanding, the condition of
the Society may be described as distinctly flourishing, our
numbers having again risen above 600. We have lost six
Fellows by death and eight by resignation; none have been
removed from the list. ‘Twenty-one new Fellows have been
elected to the Society, and M. Paun Marcuat was elected
early in the year to succeed to the Honorary Fellowship
rendered vacant by the death of Dr. Emm Frry-Gessner,
of Geneva, at the end of 1917. The Society now consists of
twelve Honorary Fellows, two Special Life Fellows, and
five hundred and ninety-one ordinary Fellows, making a
total of six hundred and five. Of those lost by death Capt.
CuHarLEs Emmett and Mr. C. JemMetr gave their lives for
their country, and Mr. C. O. Farquaarson, who was doing
admirable entomological work in Africa, was drowned in the
collision of the Burutu, when returning home on leave; the
remaining three were Mr, K. A. Acar of Dominica, the Rev.
F. E. Lowe, and Col. J. G. Prncner.
Owing to the great increase in the expense of printing,
the volume of the Transactions for 1917 will of necessity be
the smallest published for some years. It will consist of
(Galho-eay —))
327 pages, illustrated by .thirteen half-tone plates, two line
blocks and a sketch-map, and contain sixteen papers by the
following authors :—Mr. Maucoum Cameron, M.B., R.N. (2);
Dr. F. A. Dixy, M.A., M.D., F.R.S. (2); Messrs. E. Duxin-
FIELD Jones; EK. HK. GREEN; the late ANTOINE GROUVELLE
(communicated by Mr. Hucu Scorr, M.A.); J. J. Jorcry
and W. J. Kaye in conjunction; K. Kunut Kannan, M.A.;
Rev. F. D. Morice, M.A.; Mr. Frepsrick Muir; Lord
RoruscuiuD, F.R.S., F.LS., F.Z.S.; Mr. Davin SHarp,
M.A., M.B., F.R.S.; Dr. A. JEFFERIES TuRNER, M.D.; and
Mr. Rowranp EK, Turner, F.Z.8. (2). The cost of repro-
duction of Mr. DuxInFreELD JoNEs’s plates was partly borne
by the Author, and Mr. J. J. Jotcey has given the whole
expenses of the sketch-map; the cost of reproduction of all
the other plates has been borne by the Society, but the
originals have in all cases been presented by the authors.
Five papers are concerned with the Coleoptera, five with the
Lepidoptera, three with the Hymenoptera, two with the
Hemiptera, and one is on Nomenclature. The Proceedings
will consist of nearly 180 pages and one line-block plate.
At a special Meeting on November 6th an alteration was
effected in the bye-laws with the view of appointing a
professional Auditor.
The meetings have not been so fully attended as in late
years, but the papers and exhibits have fully maintained
their interest.
The Council has resolved to appoint a sub-committee to
consider the question of better accommodation for the Society,
and to approach the Government on the question, if thought
advisable, but the actual nomination of the Fellows who
shall serve upon this sub-committee has been left to the
incoming Council.
As some confusion seems to have been caused by the
apparent discrepancies between the two Lists of Fellows
published annually, it may be well to explain that the List
issued in Part V contains the names of all who have been
Fellows during any part of the year to which the Part refers,
and therefore includes the names of all those who have died,
resigned, or been removed during the course of the year,
Ceclxacare)
while the List published separately consists of the names of
those only who are actually Fellows at the time of going to
press. This latter List can only be issued, for technical
reasons, after the publication of Part V of the previous year.
The TREASURER reports as follows :—
“The Income for 1918 shows an increase on that of 1917
of £236 9s. 2d., the details of which are as follows :—
1917. 1918. Comparison.
cso. Gy Gk iS Rooms
Interest . Sie 6510 1i+ 18 7 2
Admission Fees E 25 4 0 3110 0 + Greomn0
Annual Contributions—
Current Year 390 12 0 476 14 0,/+ . 86 2 0
Arrears 45 3 0 918618 “64 [41 15°26
Sale of Publications 144 9 10 154 O11 |}|+ (Os Ul ea |
Donations— |
In Aid of Publications | 11 8 8 513 7)|— 5 Toa
ees eLearn: ss By 1415 0;+ 1112 6
3) as uibrary | 3110 O Nil: — 3110 0
£688 12 11 | £926 3 1)+ £236 9 2
“This increase in income consists very largely of increases
in the Annual Contributions, for 1918, and for arrears. It
must be remembered that the more favourable state of affairs
in this respect arises in great part owing to the severe and
prolonged illness of the late Treasurer, Mr. A. H. Jones.
“The surest test of the Society’s financial condition, from
an income point of view, is undoubtedly the number of sub-
scribers who pay their contributions within the year in which
they are due. In 1913, the year before the war, the number
of Fellows who paid their subscription within the year was
467; in 1914—the high-water mark—472; in 1915, 452; in
1916, 414; in 1917, 372; and in 1918, 455. It has been
very difficult during the past. year to get into touch with
many of the subscribers who reside in remote parts of the
world. The restrictions of intercourse will now be removed,
and I trust that at the end of this year I shall be able to
record a result as favourable as that of 1915.
“The reasons which have made it difficult to obtain sub-
scriptions for the current year apply also to the arrears, the
( clxxxii )
total of which on January Ist, 1918, amounted to £291 8s. 5d.,
due from 151 contributors. This on the 3lst of December
last had been reduced to £147 10s. 1ld., due from 69 con-
tributors. I feel quite sure that this item will be very much
less at the end of this year,
“ The expenditure has been largely influenced by the reduc-
tion in volume of the Publications. The net result of the
increase in income, and reduction in expenditure, is, that the
Society has a balance in hand, after allowing for the liabilities,
of £298 15s. 5d., as against 17s. 10d. on January Ist, 1918.
“Tt must, however, be borne in mind that the cost of
certain items of expenditure, and especially publishing, have
greatly increased during the past year. The cost of this
item over pre-war rates is about double, and although this
may, and I hope will, be modified when conditions become
normal, there is unfortunately no doubt but that a large
portion will be permanent.
“The value of the Society’s investments in consequence of
the improved national situation has increased during the year
by £68 5s. lld. In the statement of assets and liabilities
the value of the Library has not been taken into account.
In the last statement it was estimated at £3,800; probably
at the present time the value is considerably more than this;
the Library is now insured for £4,375. The Stock of the
Society's Publications is insured for £600.
“'W. G. SHELDON.
. ** Treasurer.”
The following is the Report of the Lrprartan :—
‘Three hundred and thirty volumes have been issued from
the Library for home reading. Twenty volumes and a large
quantity of Separata have been presented to the Library.
As was the case the previous year, very few foreign periodicals
have come to hand. The Library has again been largely used
for purposes of reference.”
The Report was adopted on the motion of Mr. E. E. Green,
seconded by Mr. JANson,
No alternative names having been received, the President
declared the following Fellows, nominated by the Council,
( clxxxiv )
to be appointed as Officers and Council for the ensuing
year :—
President, Comm. JAMES J. WALKER, M.A., R.N., F.LS.
Treasurer, W. G. Swuextpon. Secretaries, Rev. GEORGE
WHEELER, M.A., F.Z.8.; Dr. 8. A. Ngave, M.A., D.Sc., F.Z.S
Librarian, GEorGE CHARLES CHAMPION, F.Z.8., A.L.S. Other
Members of Council, E. C. Bepweii; G. T. Bernune-Baker,
F.LS., F.Z.S8.; Kenneta G. Bram, B.Sc.; Matconm
CamMERON, M.B., R.N.; W. C. Crawtey, B.A.; J. Hartiey
Durrant; Dr. H. Evrrineuam, M.A., D.Sc., F.Z.S8.; Dr. C. J-
GaHAN, M.A., D.Sc.; Dr. A. D. Imus, M.A., D.Sc., F.LS.;
Dr. G. A. K. Marswatt, D.Sc., F.ZS.; Rev. F. D. Morice,
M.A., F.Z.S.; Herpert EK. Pace.
The PrEsIDENT then delivered an Address, after which a
Vote of Thanks to him was proposed by Dr. Lonestarr, and
seconded by Mr. J. H. Durrant, to which Dr. GaHan made.
a reply.
Prof. Poutron then proposed a Vote of Thanks to the
other Officers, remarking on the difficulties with which they
had had to contend this year and on the flourishing condition
of the Society notwithstanding. This was seconded by Mr.
R. Apxin. The TREASURER and both SECRETARIES said a
few words in reply.
THE ENTOMOLOGICAL SOCIETY OF LONDON.
TREASURER’S ACCOUNTS for the Year ending December 31, 1918.
Presented at the Annual Meeting, January 15, 1919.
RECEIPTS AND PAYMENTS ACCOUNT.
RECEIPTS. PAYMENTS.
n5 EA CE Li ess de
To Balance as_ per last Byglenitiercea reste ssiatecs we ees DO) ole
Account we Salarieseu@ sce! cece ss O0U O 20
General Account £294 18 8 » Library—
Westwood Be- New Books ... £4122
quest Fund... 87192 Binding Repairs
—§ 382 17 10 and Insurance 18185
», Interest on Investments— —— 2310 7
Dividend on ,, Cost of Publications—
Consols’ ... £33170 Printing... £24015 1
Interest on De- Illustrations 50 14 3
POSIUy caer seer LA ONS, Distribution 20 91
Interest on —— 311 18 5
Birmingham » Sundry Printing and
% Stock... 7 38 Stationery” =..s se) ses, p20) ‘Oe
-—. 55 10 1} ,, Postage .. 5B Allajes Pa)
, Admission Fees bean) cee eo Lal OPanOl eres Tea and Light Refreshments 13 19 0
A ” ‘Annual Con- | ,, Miscellaneous Payments... 16 4 8
tributions 1918 £476 14 0 », Balance at Bankers—
Avrearses 2.4...) ol86, 18/6 On General
In Advance... 21 00 Account ...£725 167
—— 684 12 6} On Tea Fund
py COMPOSiblOnSy <cepqcem | =s- oP 15 0} Account... 110
,, Sales of Publications meee kay, Urea lat ——
,, Donations— £726 7 7
In aid of Pub- On Westwood
lications ... £5137 Bequest Fund
In aid of Tea Account... 95210
Hunde. oe el4al5 (0 821 10 5
—— 20 8 7| ,, Cash in hand on Tea Fund
| FACCOUM tiene tcee acct) bose 5. 0
£1,344 14 11 £1; 344 11411
WESTWOOD BEQUEST FUND.
Giese ad. £$ s. ad.
To Balance at Bank, Jan. 1, 3y Expenditure on Illustra-
1918 aa os. Ou) LOE HIONSie pes. see eee oes =
- cert on Birmingham » Balance at Bank, Dec.
Corporation 3 % Stock 7 3 8 Sl LOS ee Wee es.ce hess OO moe LO.
£95 2 10 £95 210
TEA FUND.
ose ca S$ st ds
To Donations... ... ... ... 1415 0 By Teaand Light Refreshments 13 19 0
», Balance at Bank,
Dec. 31, 1918 £ 11.0
»» Cash in Treasurer’s
Nandseess sec cee)
£14 15 0) £14 15 0
W. G. SHELDON, 7reasurer.
We have examined the above Account of Receipts and Payments with
the Books and Vouchers produced to us and certify it to be in accordance
therewith.
The Bankers have certified the correctness of the Cash Balance, and that
they hold the Securities for the Investments.
(Stgned) W. B. Kren & Co., Chartered Accountants.
23, Queen Victoria Street,
London, E.C. 4.
January 13, 1919,
( clxxxvi )
MEMORANDUM
AS TO ASSETS AND LIABILITIES AT DECEMBER 31, 1918.
ASSETS. | LIABILITIES.
£ os. d. Gy sae
To Arrears of Annual By Cost of Printing Trans-
Contributions... £147 10 11 | actions Part V, 1917; Parts
Less Amount not I—V, 1918: Cost of Plates
and Sundry Unpaid Ac-
considered good 6310 11
84 00. counts; and Cost of Postage
Present value of— on Transactions due_ to
” ch . -
£1,354 2s. 2d. Fellows residing abroad and
Consols 24 % at present undelivered .. o28 00
at 59 (cost
£15233 3s.) ... S198 17
£239 12s. 4d.
Birmingham
Corporation
3% Stock at
62 (cost £250) 14816 0
bo
947 13 2}
,, Balance at Bankers, Dec. 31, |
1918—
On Deposit Ac-
count ... ... £600 0 0
On Current Ac-
count... =.) 22105
——— §21105
W. G. SHELDON, Treasurer.
( ‘elxxxvi' |)
GENERAL INDEX.
The Arabic figures vefer to the pages of the ‘Transactions’; the Ronan
numerals to the pages of the ‘ Proceedings.’
GENERAL SUBJECTS.
Aberrations, of British Rhopalocera, exhibited, cliii; on the naming of, 115.
Africa, observations on the seasonal forms of butterflies, etc., in ex-German
Kast, lvili, Ixxxvi; bud and flower-like //atidae (Homoptera) from ex-
German Kast, exhibited, Ixxviii; almost exclusively east of Lake Tanga-
nyika, further notes on ex-German East, Ixxxviii; Rhopalocera from
South Central, exhibited, clxxvi.
African Veterinary Corps in 1916, journeys of Capt. W. A. Lamborn with the
Hast, xl.
Agrias narcissus, series of, exhibited, lvii.
American genus Asty/us (Coleoptera), with descriptions of their sexual char-
acter, notes on various species of the, clv.
Anal tufts to the brands of the hind-wings observed and the scent perceived
in a male Danaine butterfly, the relation of the, elxxii.
Androconia in Orders other than Lepidoptera, lvi; androconial scales in saw-
flies, exhibited, lviii.
Anobium striatum and A. pertinax, the ‘tapping ” of, lvii.
Ant from Java, nest of, exhibited, li.
Appeal, from Essex Field Club ve pension fund for their Curator, liv; towards
upkeep of Wicken Fen, liv.
Astylus (Coleoptera), with descriptions of their sexual character, notes on
various species of the American genus, clyv.
Australian, sawflies, especially ‘“ Authors’ Types” and the specimens in the
British Museum of Natural History and the Hope Collection in the
Oxford University Museum, with diagnostic synopses of the genera and
species, notes on, clviii, 247; Braconidae in the British Museum, 91.
Barrackpore, flight of winged Termites at, lxiv.
Bees, giantism in male, exhibited, Ixvii.
Beetle, new British and rare, exhibited, i.
Blood-sucking Diptera on new-comers into the tropics and of their gradual
diminution, suggested interpretation of the special attacks made by,
elxxiv.
Braconidae in the British Museum, Australian, 91,
Britain, beetle new to, exhibited, 1; captures of Polistes gallica in, \xvi;
Dipteron new to, exhibited, Ixxvii.
( clxxxvii )
British Museum, of Natural History and the Hope Collection in the Oxford
University Museum, with diagnostic synopses of the genera and species,
notes on Australian sawflies, especially ‘‘ Authors’ ‘lypes,” and the speci-
mens in the, elvili, 247; Australian Braconidae in the, 91.
British Rhopalocera, aberrations of, exhibited, cliii.
Butterflies, etc.,in ex-German East Africa, observations on the seasonal forms
of, lviii, lxxxvi; captured in Natal during the extraordinary rains of 1917,
exhibited, Ixxxiv ; of the genus Castnia and a mimetic Hesperid, exhibited,
elxiv; of New Guinea, on mimicry in certain, 118.
Butterfly vision, elxxviii.
Bye-law, proposed alteration of, Ixxvi, elv, clix, clxi.
“‘ Camouflage,” modern use of word, Ixxvii.
Castnia and a mimetic Hesperid, butterflies of the genus, exhibited, elxiv.
Catagramma, two species of, exhibited, ii.
Catocaline moth, Egybolis vaillantina, seized and dropped by a bird at Durban,
the conspicuous, xxvii.
Catochrysops phasma, not C. parsimon, proved to be myrmecophilous, Ixxix.
Chaleid in undigested seed, exhibited, elxiv.
Charaxes ethalion and C. etheocles, and bred male-like females of the latter,
new mimetic female forms of, exhibited, Ixxix.
Coccid, rare, exhibited, clix.
Coceus viridis, a mutant from Pulvinaria psidiz, an instance of mutation,
130.
Cockroach, outdoor specimen of, exhibited, elvii.
Coleoptera, longevity of larva of, exhibited, lii; notes on the ontogeny and
morphology of the male genital tube in, clv, 223; with descriptions of
their sexual character, notes on various species of the American genus
Astylus, clv; of the families Ostomidae, Monotomidae, Colydiidae and
Notiophysidae from the Seychelles and Aldabra Islands, 1.
Colour-inheritance in Pediculus humanus, experiments in, clvil.
Colyditdae and Notiophysidae from the Seychelles and Aldabra Islands,
Coleoptera of the families Ostomidae, Monotomidae, 1.
Cossidae and on the classification of the Lepidoptera, observations on the
Lepidopterous family, lv, 155.
Council, nomination of, elxvii, clxix.
Cremastogaster ants in S, Nigeria, Harpagomyia and other Diptera fed by,
XXX.
“ Cuckoo-spit” by Philaenus spumarius, method of formation of, cliii, elxv.
Culicid Toxorhynchites bred in 8. Nigeria, exhibited, xxxix.
Danaida chrysippus f. dorippus in ex-German East Africa, new form of
Pseudacraea pogget mimicking, v.
Danaine butterfly, the relation of the anal tufts to the brands of the hind-
wings observed and the scent perceived in a male, clxxii.
Dioptid moth, mimetic association of Ithomiine butterflies and rare, exhi-
bited, 1.
Diptera, fed by Cremastogaster ants in S. Nigeria, Harpagomyia and other,
xxix; collected in S. Nigeria, myrmecophile, exhibited, xxxix; new to
Britain, exhibited, lxxvii; on new-comers into the tropics and of their
gradual diminution, suggested interpretation of the special attacks made
by blood-sucking, clxxiv.
Ge clxxxixe )
Drosophila and the inheritance of small variations, the fruit-fly, xxii.
Durban, the conspicuous Catocaline moth, Eyybolis vaillantina,. seized and
dropped by a bird at, xxvii.
Dynamine, new, exhibited, 111.
Dytiscus margtnalis, larval skins of, exhibited, clvii.
Egybolis vaillantina, seized and dropped by a bird at Durban, the conspicuous
Catocaline moth, xxvil.
Epitola urania, exhibited, xxiii.
Ergatandromorph of Myrmica sulcinodis, exhibited, clvii.
Essex Field Club, appeal ve pension fund for Curator of, liv.
Ethiopian species of Sarangesa and other Hesperidae, the habits of, xxvi.
Eupithecia helveticata var. arceuthata and a living larva, exhibited, clix.
. Farquharson, C. O., notice of deatb of, clxvii.
Fellows, election of, i, xxxix, liv, lv, Ixxvi, clxil, clxvii, clxx.
Fiji, the Hymenoptera of, clxix, 334.
Flatidae (Homoptera) from ex-German East Africa, bud-and-flower-like,
exhibited, Ixxviii.
French Guiana, species of He/icontus from, exhibited, clii; in 1917, compared
with a similar collection made in 1915, notes on a large Heliconine col-
lection made in, elxvii, 347.
Genital tube in Coleoptera, notes on the ontogeny and morphology of the
male, clv, 223.
Giantism in male bees, exhibited, ]xvii.
Glutophrissa epaphia and Phrissura sabina distinguished by their scent-scales,
the males of, exhibited, clxx.
Harpagomyia and other Diptera fed by Cremastoyaster ants in 8. Nigeria,
XXIX.
Heliconine collection made in French Guiana in 1917, compared witha similar
collection made in 1915, notes on a large, elxvii, 347.
Heltconius from French Guiana, species of, exhibited, clii; new sub-species of
H., erato, exhibited, clx.
Hemaris from the New Forest, both species of, exhibited, clv,
Hemiptera, ova of, exhibited, i.
Hesperid, butterflies of the genus Castnza and a mimetic, exhibited, clxiv.
Hesperidae, the habits of Ethiopian species of Sarangesa and other, xxvi.
Homoptera from ex-German East Africa, bud-and-flower-like Flatidae, exhi-
bited, Ixxviii.
Honorary Fellow, election of, lv.
Hymenoptera, Sesias mimics and not models of, xxix; of Fiji, the, elxix,
334.
Hypolimnas (Euralia) dubia f. wahlbergi at rest in same spot after a week’s
interval, xxiii.
Isle of Wight, Musca autumnalis hibernating in a loft in the, exhibited, xxii.
Ithomiine butterflies and rare Dioptid moth, mimetic association of, exhi-
bited, 1.
Java, wasps’ and ants’ nests from, exhibited, li.
Jugo-frenate genera of Micropteryyidae, liii.
Lamborn with the East African Veterinary Corps in 1916, journeys of Capt.
Wi -Ace xe
Larva of Lupithecia helveticata var. arceuthata, exhibited, clix.
(gexec: 9)
Larval skins, of Dytiscus marginalis, exhibited, clvii, clxi; of Hydrophilus
piceus, exhibited, clxi.
Lepidoptera, androconia in Orders other than, lvi.
Lepidopterous family Cossidae and on the classification of the Lepidoptera
observations on, lv, 155.
Leptothorax acervorum, monstrosity in, exhibited, cliii.
Lice and trench fever, lvi.
Longevity of Coleopterous larva, exhibited, lii.
Lulanguru and St. Michael’s Mission, Pierines from, exhibited, cl.
Lycaena alcon, life-history of, exhibited, clv; bred L. avion, exhibited, clxviii.
Lycaenidae and other butterflies, etc,, observations of Dr. Th. Mortensen on
the “ false head”? of, xliv,
Lycaeninae bred from larvae feeding on a single species of Loranthus, 8. .
Nigerian, exhibited, Ixxix.
Macedonian Orthoptera, exbibited, cl xiii.
Mechanitis polymnia, darkening of hind-wing in, exhibited, clxix.
Meeting, discussion as to time of, lvii.
Micropteryyidae, jugo-frenate genera of, liii.
Mimetic, association, Pseudacraeas in, exhibited, v ; new form of Pseudacraea
pogyet mimicking Danaida chrysippus f, dorippus in ex-German East
Africa, v; association of Ithomiine butterflies and rare Dioptid moth,
exhibited, 1; female forms of Charaves ethalion and C. etheocles, and
bred male-like females of the latter, new, exhibited, lxxix; Hesperid,
butterflies of the genus Castnia and a, exhibited, elxiv.
Mimicry in certain butterflies of New Guinea, on, 118.
Molippa simillima, a correction, 117.
Monotomidae, Colydiidae and Notiophysidae from the Seychelles and Aldabra
Islands, Coleoptera of the Families Ostomidae, 1.
Monstrosity in Leptothorax acervorum, exhibited, cliii.
Morpho eugenia, new form of, exhibited, clxviii.
Mortensen on the “false head” of Lycaenidae and other butterflies, etc.,
observations of Dr. Th., xliv.
Musca autumnalis hibernating in a loft in the Isle of Wight, exhibited, xxii.
Mutation: Coceus viridis, a mutant from Pultinaria psidi?, an instance of,
130; some remarks on paper “ An Instance of,” 149.
Myrmecophile Diptera collected in S. Nigeria, exhibited, xxxix, Ixxix.
Myrmica sulcinodis, ergatandromorph of, exhibited, elvii.
Naming of local races, subspecies, aberrations, seasonal forms, etc., on the,
115.
Natal during the extraordinary rains of 1917, butterflies captured in, exhi-
bited, Ixxxiy.
Nests from Java, wasps’ and ants’, exhibited, li.
Neuroptera from Salonica, exhibited, clxx.
New Forest, both species of Hemarzs from the, exhibited, clv.
New Guinea, on mimicry in certain butterflies of, 118.
Nidification of Osmda aurulenta, correction as to, xl.
Nigeria, Hurpagomyia and other Diptera fed by Cremastogaster ants in 8.,
xxix; myrmecophile Diptera collected and the Culicid Tovorhynchites,
bred in S., exhibited, xxxix; bred from larvae feeding on a single species
of Loranthus, Lycacninae from 8., exhibited, ]xxix.
(@yexc.#)
Notiophysidae from the Seychelles and Aldabra Islands, Coleoptera of the
Families Ostomidae, Monotomidae, Colydiidae and, 1.
Obituary. CC. O. Farquharson, ¢lxvii.
Officers, nomination of, elxvii, clxix.
Orthoptera, from Salonica, exhibited, clxiii; Macedonian, exhibited, elxiii.
Osmia aurulenta, correction as to nidification of, xl.
Ostomidae, Monotomidae, Colydiidae and Notiophysidae from the Seychelles
and Aldabra Islands, Coleoptera of the Families, 1.
Oxford University Museum, with diagnostic synopses of the genera and
species, notes on Australian sawflies, especially “ Authors’ Types ” and the
specimens in the British Museum of Natural History and the Hope Col-
lection in the, clviii, 247.
Pararge megaera, black form of pupa of, exhibited, lv ; confirmation of con-
clusion that eayly pale spring form of P. aegeria race eyerides is produced
from over-wintering pupae, exhibited, lx ; further notes on P. aeycria race
egerides, \xil.
Pediculus humanus, experiments in colour-inheritance in, elvii,
Philaenus spumartus, method of formation of “ Cuckoo-spit” by, cliii.
Phrissura sabina distinguished hy their scent-scales, the males of Glutophrissa
epaphia and, exhibited, elxx.
Pierines from Lulanguru and St. Michael’s Mission, exhibited, cl.
Pinacopteryx, the charina group of, xxv, 191.
Polistes gallica, British captures of, xvi.
Prects octavta, local race of, exhibited, clxxvii.
Pseudacraeas in mimetic association, exhibited, v; new form of P. poygei
mimicking Danaida chrysippus t. dorippus in ex-German East Africa, v.
Pulvinaria psidti,an instance of mutation, Coccus viridi’s, a mutant from
130.
Pupation of Timarcha tenebricosa, exhibited, ]xxvii.
Races, on the naming of local, 115.
Rhopalocera, aberrations of British, exhibited, cliii; from South Central
Africa, exhibited, elxxvi.
Rhyncophora, a preliminary note on the male genitalia, studies in, clv, 209.
St. Michael’s Mission, Pierines from Lulanguru and, exhibited, cl.
Salonica, Orthoptera from, exhibited, clxiii; Neuroptera from, elxx.
Sarangesa and other Hesperidae, the habits of Ethiopian species of, xxvi.
Sawflies, androconial seales in, exhibited, lviii ; especially “ Authors’ Types ”
and the specimens in the British Museum of Natural History and the
Hope Collection in the Oxford University Museum, with diagnostic
synopses of the genera and species, notes on Australian, clviii, 247.
Scent perceived in a male Danaine butterfly, the relation of the anal tufts to
the brands of the hind-wings observed and the, elxxii.
Scent-scales, the males of Glutophrissa epaphia and Phrissura sabina dis-
tinguished by their, exhibited, elxx.
Seasonal forms, of butterflies, etc., in ex-German East Africa, observations
on the, lviii, Ixxxxi; on the naming of, 115.
Sesias mimics and not models of the Hymenoptera, xxix.
Seychelles and Aldabra Islands, Coleoptera of the families Ostomzdae, Mono-
tomidae, Colydiidae and Notiophysidae from the, 1.
Singapore, new Staphylinidae from, clv, 58, 231.
°
Pa
( “excin ?)
Staphylinidae from Singapore, new, elv, 58, 231.
Stylops and “assembling” of the males, observations on the pairing of, Ixx.
Subspecies, on the naming of, 115.
“Tapping ” of Anobdum striatum and A. pertinaa, the, lvii,
Tea fund, discussion as to, clix, clxii.
Termites at Barrackpore, flight of winged, lxiv.
Timarcha tenebricosa, pupation of, exhibited, lxxvii,
Toxorhynchites bred in 8. Nigeria, Culicid, exhibited, xxxix.
Trench fever, lice and, lvi.
Vice-Presidents, nomination of, i.
Vision, butterfly, clxxviii.
Wasp from Java, nest of, exhibited, li.
Wicken Fen, appeal towards upkeep of liv.
( exci )
SPECIAL INDEX.
The Arabic figures vefer to the pages of the ‘ Transactions’ ; the Roman numerals
to the pages of the ‘ Proceedings,
abdominale (Conosoma), 235
abdominalis (‘Trichorhachus), 261
Abia, 282, 323, 325
Abietinus, 318
Abiides, 262
abnormis (Appias), 120, 122
(Delias), 119, 122
var. euryxantha
119
a (Huphina), 118, 120, 121,
122, 123, 124, 126, 127,
128
(Pieris), 120, 122
3 (Tachyris), 118, 119, 122
Acantholophus, 225
Acanthoperga, 330
acara (Acraea), cx
acervorum (Leptothorax), cliii
achaemenes (Charaxes), Cxix, xxi
avhine (l'eracolus), cli, elii
Acidalianae, 186
acis (Thecla), xlv
Acraea, Cli, Cviii, eX, CXXXi11
Acraeinae, xlii, xliv, exvill
acrita (Acraea), lix, lxxxvil
»» acrita (Acraea), evil
ambigua (Acraea), lix, Ixxxvii,
cii
»»» manea (Acraea), lix
)
(Delias),
39
”
%)
actia (Precis), cxiil, cxxvii, cxxviil,
CXXX, CXXxil
> & tureata (Precis), ¢xxvil;
: CXXVili, CXxx
actinias (Dudgeona), 156, 157, 179
acuminatum (Lecanium), 134
acuminatus (Aphanocephalus),
555 57
acutissimus (Coccus), 135, 136
Acyttara, 165, 178
ada (Tachyris), 119
Adinopsini, 242
Adinopsis, 242
2,
PROC, ENT. SOC. LOND., V. 1918.
adonis (Morpho), ¢lxviii
aegeria (Pararge), ]xii
» race egerides (Pararge),
Lxii, Lxiii, lxiv
aelia (Hypoleria), li
aeratus (urys), 296
aesculi (Zeuzera), 163
affinis (Chalcosia), 176
(Perga), 267, 268, 282
es
99
africanum (Coccus), 136, 138, 139,
145
+ (Lecanium), 150
africanus (Peltis), 4
aganippe (Delias), 125, 127
agatha (Dynamine), ili
» (Neptis), exiv:
Agathiella, 108, 110
agathina (Mylothris), citi
Agathinae, 106
Agathis, 110
agnata (Huphina), 120
», (Perga), 268, 284
Agrotis, 183
Alaena, Ixxxvil
alamanus (Aleimus), cxix
albicosta (Lentagena), 165
albimaculata (Amauris), xliii
albisectus (Parasphex), exlvi
55 (Sphex), exlvi
albiventris (Pachylostieta), 326
33 (Plagiocera), 326
albocinctus (Probolus), 345
albofimbriatus (Lithurgus), 336
albomaculata (Prosthesima), xevii
alcibiades (Argiolaus), xxix
alcon (Lycaena), clv, elvi, elvii, elxix
Aletis, exxxiv
Alindria, 3
Allantus, 324
alluaudi (Mychocerus), 2, 45, 47
amalda amalda (Leucothyris}, li
amaldina (Leucothyris), 1, li
N
”
‘ ( cxciv, 4) =
amalia (Huphina), 119
», (Pieris), 119
amanga (Axlocerses), exiii, Cxxxii
Amasis, 323
Amauris, xlii, xliii, xliv, exvi, exvii,
elxxil
amenaida (Neoperga), 331
on (Perga), 280
9 (Xyloperga), 286, 331
Ammophila, exxxy
ampliatus (Lycus), exxxix
Ampulicinae, exxxv
anachoreta (EKulissus), 83
anacreon (Acraea), lix
,, bomba (Acraea), lix
analis (Amphidesmus), exxxix, ex]
», (Pterygophorus), 290, 2
Andrena, Ixvii, ]xviii, xix, lxxii
Andreninae, 336
anemosa (Acraea), Civ, CXVili, Cxxiv
angulatus (Odontomachus), 334
annae (Teravolus), cli
annulatum (Megalommum), 97
annulipes (Arge), exxxix
*s (Hylotoma), exxxix
anomala (Gonatopus), 341
Anommatus, 24
ansorgei (Charaxes), Ixxxi
- (Hibrildes), exxxiv
Antargidium, 254, 259, 325, 332
antheus nyassae (Papilio), exvi
Anthribidae, 214, 215
antilope (Precis), xxvii, lx, exxiv,
CXXVili, CXxx, cxxxii
simia (Precis), ¢xxiv,
CXXVill, CXxX
antiopa (Perga), 270, 276, 277, 283
antipoda (Monostegia), 316, 332
Aphanocephalus, 48
Aphelinae, 341
aphnaeoides (Epamera), ciii
apicale (Antargidium), 25
» (Hylotoma), 254, 303
apicifumatus (Henicospilus), 345
Apidae, 336
Apiogaster, cx]
Apionidae, 214
Apioninae, 209
Apistini, 7
Apocrita 308
Apoda, 177, 178
appendigaster (Evania), 341
ce (Ichneumon), 341
Appias, e]xx, elxxi, 120, 122
archesia (Precis), lix, exxiv,
CXXVl, @XXvil,
CXXX, CXXXIi
a f. limnoria (Precis), lix
3 f.
CXXV,
CXX Vill,
archesia f. pelasgis (Precis), cexxv,
CXXVi, CXxVii,
C@XXVlli, Cxxx
a 33 var. chapunga
(Precis), exxvi
3 f, semitypica (Precis), exxvi,
CXXVill, CXXX
PA f. staudingeri (Precis), cxxv,
CXXVi, CXXVIll, CXxx
Arctiadae, 182, 184, 187, 188
Arge, 254, 802, 325, 327
argenthona (Delias), 125
Argides, 259, 260
Arginae, 253, 254, 260, 304, 322, 323,
324, 325, 327
Argini, 262
Argiolaus, xxxii, xlviii, lx
argolis (Nepheronia), 128
arion (Lycaena), clvi, elvil,
clxix
Arrhenophanes, 174
artaxia (Precis), xxvii, exxiv, exxvil,
CXXV1li, CXXX, CXXXI1
» f. nachtigalli (Precis), exxvil,
CXXViil, CXXx
» f. nobilitata (Precis), exxvil
CXXVill, CXXX
aruna (Delias), 126, 127
aruncella (Micropteryx), liv
Asilidae, cxxxvii
aspericolle (Calliderma), 80
Astata, xcix
asterope (Yphthima), exiii
astrigera (Acraea), ex, ¢xvili
Astylus, elv
aterrima (Stylops), Ixxi, Ixxii
Athalia, 302, 304, 322, 325
atrata (Clarissa), 258, 300
atratus (Polyclonus), 257
Attelabidae, 214
atymnus (Castnia), 175
aurantiaca (Alaena), exxxiii
auricularia (Forficula), elxiii
aurulenta (Osmia), x1
#4 (Perga), 278
fr (Xyloperga), 278, 281
australiensis (Campyloneurus), 99,
Povey 100
australis (Culama), 159
ae (Schizocera), 259
5 eke 253
» (Stygia), 159
» (Trichorhachus), 259, 260
autumnalis (Musca), xxii
aversata (Eois), 186
Axiocerylon, 7, 41, 42
azota (Charaxes), exviii, exix, exxl
Azygophleps, 162
elxviii,
(
bakeri (Delias), 125
bakewelli (Enarsus), 225
balteata (Gametis), exxxix
» (Glyeyphana), cxxxix, exl
basalis (Ingurimorpha), 164
basipennis (Stigmatobracon), 92
batis (Thyatira), 183, 185
battus (Thecla), xlv
Belenois, Ixxxvii, cii, cili, eviii, exii,
exvii, cli
Belidae, 212, 214
belinda (Perga), 271
belisama (Delias), 127
bella (Euryopsis), 258, 295
» (Perga), 263, 264, 265, 269, 271
277, 278, 283, 285
», var. nigra (Perga), 278
belli (Epitola), xxv
bellosus (Merinotus), 99
Belonogaster, cx
belonuchoides (Philonthus) 88
Belus, 212, 226
bembesiana (Notogonia), exxxix
Bembex, ci, exlv
Bengalia, xxxiii
beninensis (Ammophila), xcix, cxxxy,
CXXXVi
Berytus, li
betulae (Pulvinaria), 146
Shima, 180, 181
bicolor (Callilestes), exlii
5, (Mystrocnemis), ex]
», (Perga), 276
bicosta (Palaeosia), 182
biernciatum (Lecanium), 134
hidentatus (Belonogaster), 338
bifasciatus (Pterygophorus), 248, 290,
293
himaris (Bracon), 93
binotatum (Conosoma), 236
binotatus (Aphanocephalus), 2, 50, 56
bipustulatum (Conosoma), 233
bisecta (Perga), 270, 271
bispinus (Stenus), 68, 69
bituberculatum (Lecanium), 134
bizonatus (Odynerus), 339
Blattidae, exxxiv
Boarmianae, 185
boebera (Nepheronia), 128
boeticus (Lampides), xlvili
bohemanni (Charaxes), Ix, exvill, exix,
CXX, CXXi, c]xxvi
boisduvalii (Pseudacraea),
CXill, CXX1V
Bombycidae, 187, 189
bombyliformis (Hemaris), clv
3ombyliidae, exxxvii
Bothrideres, 7, 28
Vil, Xl;
| castaneae (Phragmatoecia), 161,
excv )
30 hriderini, 28
bovistae (Caenocara), ti
bowkeri (Stugeta), eviii
Brachyceridae, 214
Brachyeerus, 215
brachypterus (Pinophilus), 70
Brachyxiphus, 314
Bracon, 93
Braconidae,
Braconinae, 91
Brenthidae, 214, 217
breve (Conosoma), 234
brevipalpis (Toxorhynchites), x]
brevitarsis (Perga), 268
brigitta (Terias), cxiv, cl, cli
brullei (Perga), 272, 284
brunneicollis (Coproporus), 238
brutus (Charaxes), 1xxx
buchneri (Cremastogaster), x]
re alligatrix (Cremastogaster)
xl
Bupalus, 185
buyssoni (Perga), 282
caeneus (Delias), 125
caerulans (Sphingonotus), clxiv
caerulea (Rapala), evii, cix
caespitum (Tetramorium), clvii
caffra (Bromophila), ¢
Calandridae, 211, 213, 214, 217
caldarena (Acraea), cx, ¢xiv
5 f. neluska (Acraea), ex
Caliroa, 257, 259
callidia (Teracolus), cli
cameronii (Acanthoperga), 330
a (Perga), 275, 330
Camponotinae, 335
Camptoperga, 330
Campyloneurus, 99
capita (Diplotoma), 2,17
capitator (Pracon), 94
capparidis (Lecanium), 134
capreae (Lecanium), 134
capricornus (Pinacoy teryx), 191
Capsidae, cxxxix
Carabidae, Ixxvili, xevii, xii, ¢XxXXiv
carinata (Colobopsis), 336
carinatus (Camponotus), 336
sa (Colobopsis), 336
sarinicollis (Thinocharis), 73
Carpocapsa, 171
casta (Teracolus), exvii. cl, cli, clii
,, f. sipylus (Teracolus), cl
castalis (Teracolus), ciil
vastanea (Perga), 269, 277, 283, 285
il
exli, exlii, 93, 96, 99, 345
”
180
castaneipennis (Philonthns), 87
castaneus (Hypostenus), 69
(
castaneus (Stenus), 69
Castnia, elxv, 175
Castniadae, 166, 175,182, 187, 188
Catochryso; s, xxxi, lxxix
Catopsilia, cli, exvii
caudata (Neoeurys), 298, 299
cavicolle (Axiocerylon), 2, 42, 47
cavicollis (Ditoma), 2, 10
cebron (Pinaco}teryx), 191
Celeuthetides, 219
celimene (‘Teracolus), ciii
centromaculata (Ithomia), li
Cephidae, 313, 314, 319, 320
Cephini, 319, 320, 321
Cephus, 309
Cerambycidae, ex]
Cerealces, 253, 255, 259, 287, 3
Ceria, ex
Cerioides, cx -
Cerostoma, 173
Cerylinae, 28
Cerylini, 30
Cerylon, 7, 30 ;
cerymica (Ploetzia), xxvii
Cetoniidae, cxxxv, cxxxix
chaeribula (Acraea), lix
Chalastogastra, 249, 308, 315
Chalcidica, 162
Chalcididae, 341
Chaleosia, 176, 177
chalybea (Perga), 274
championi (Conosoma), 236
Charaxes, Ixxx, Ixxxi, Ixxxiv, cxii,
Cxill, CxXvili, Cxix, cxxxv, clxxvi
charaxus (Mutilla), xevii
charina (Pinacopteryx), Ixxyv, 191,
192, 193, 194, 195, 197, 198, 199,
200, 201, 202, 206, 207
Cheloninae, 345
Chelura, 176
Chimabacche, 173
Chlamydinae, exxxviii
chlorotica (Shoguna) 5
christii (Perga), 265, 266, 272, 273, 2
Chrysididae, 299
chrysippus (Danaida), vi, vii, viii, ix,
XK, Xi, XU, XV, XV, Xvil;
VUE. RLS, kX EMI.
CXVill, CXXXiV
. albinus (Danaida), x
f. ale ippoides (Danaida), x
f. aleippus (Danaida), xvii,
Xvili
f. dorippus (Danaida), ix, x,
Xi, XM, dil, XW, cev
XVil, XVill, XX1, UXxil,
xlii
chrysippus Limnas), xi, xii, xviii
9
“
Un ooe,
78
>
exevl
)
chrysops (Osmylus), elxx
Cicindelidae, exxxiv
Cicones, 6, 12, 16
cihatum (Lecanium), 134
Cimbex, 323, 325
Cimbicides, 262
Cimbicinae, 304, 322, 323
Cimbicini, 262
cimicoides (Naucoris), ii
cinctus (Pterygophorus),
292, 293
cinerea (Nepa), i
cingulatus (Holisus), 85
cinnamomea (Dinopsis), 243
Cionus, 211, 216
circumductus (Philonthus), 88
cithaeron (Charaxes), 1xxx
citricola (Coceus), 130, 146, 147
Clania, 178
Clarissa, 258, 259, 295, 299, 300, 332
clarkella (Andrena), Ixvii, lxviii
clarkii (Pseudacraea), xiv
clavimaculatus (Iphiaulax), 97
clavis (Tachyris), 119
cleodora (Eronia), exiv, exvii
Cuissostages, 174
Coecidae, xxxvlii,
150, 153, 154
coecineus (I[phiaulax), exlii
Coccus, 1338, 142, 143
coelestina (Precis), exxvi
coffeae (Zeuzera), 163
colemani (Coccus), 135, 136, 142,
144, 145, 147, 148, 149
Coleoptera, cxxxix, exl, 209, 210, 211,
215
Colobicones, 6, 15
Colobicus, 6, 16
Colydiidae, 2, 5
Colydiinae, 7
Colydiini. 28
compactus (Cicones), 2, 6, 14
(Dorealaemus), ev
247, 291,
130, 131, 146, 149,
143,
99
| concolor (Lissopimpla), 344
concordia _ (Crenidomimas),
exxill, ¢lxxvii
CXXxH,
_conferta (Penthelispa), 9
_confertus (Penthelispa), 9
AP (Pyenomerus), 2,
contfrater (Trypoxylon), ¢ af ii
confusa (Belenois). clxxi
,, (Phrissura), elxxi, elxxii
», (Pieris), elxxi
coniata (Belenois), clxxi
Copridae, exxxiy
Cordyceps, Xxxii
| corones (Miresa),
| », (Susica),
( exevii )
Cossidae, lv, 155, 159, 160, 166, 171,
174, 177, 178, 188, 189, 190
Cossodes, 156, 157
Cossus, 157, 158, 168, 174, 188
cossus (Cossus), 168
costigera (Gargetta),
costulata (Alindria),
Coxelini, 24
Crabro, xcix
Crabroninae, 337
crassa (Xyleutes), 161, 162
crassicaudis (Cyanopterus), 94, 95
crawshayi (Hibrildes), cxxxiv
Cremastogaster, XXX, XXXi, XxXiii,
XXXIV, XXXV, XXXVi, XXXVii, XXXViii
crenata (Ditoma), 10, 11
erenatus (Hylesinus), 226
Crenidomimas, cvii, exi, ¢xiii, cxx,
Cxxli, exxill, elxxvli
Crenis, exx, xxii, exxiii
cressonii (Camptoperga), 330
(Perga), 272
cribratus (Orthidus), 89, 90
crispatus (Sisyphus), exlvii
cristatus (Camponotus), 335
Cryptocephalinae, cxxxviil
Culama, 159, 161, 170
Culicidae, xl
cupanae (Pulvinaria), 144
cupreipennis (Orthidus), 89
cupricollis (Ececoptoptera), xevili
Curculionidae, 214
curtulum (Cerylon), 2, 24, 40, 41, 45,
48
182
2, 3
cyaneus (Pterygophorus), 290, 292,
293
Cyanopterus, 93, 94, 96
cyanopterus (Zethus), li
cyara (Phylaria), ciii
cyathiformis (Cerealces), 287
Cyclosia, 176
eydno (Heliconius), 350
galanthus (Heliconius), 350
», hermogenes (Heliconius), 350
eygnus (Pterygophorus), 293
cylinda (Coenides), xxvii
Cymatophoridae, 184
Cynipidae, 315
Dacnochilus, 76
Dactylopinae, 145
daedalus (Hamanumida),
19
CX) Cxx,
elxxvii
dahlbomii (Verga), 266, 272, 273,
284
3 (Pergadopsis), 330
dalmanni (Perga), 276
dardanus (Papilio), viii, xlii, exiv,
exvil
dardanus f. cenea (Papilio), xxviii,
CXl1v, Cxvii
hippocoon (Papilio),
XXViil, exvil
f. lamborni (Papilio), xliii
f. planemoides (Papilio),
vii, viii
trophonius
xxviii, xlili
darwinii (Hyptiogaster), 342
dasypus (Dinarchus), ¢)xiii
debilicornis (Hypomedon), 75
decemnotata (Lissopimpla), 343
deceptus (Eurys), 258, 294, 297
decorata (Megarthropsis), 232
deflexus (Holonychus), 219
Delias, 118, 119, 120, 121, 122, 123,
124, 125, 126, 127, 128
demodocus (Papilio), exvii
dentata (Colobopsis), 336
Ne (Xyloperga), 281
dentatus (Camponotus), 336
sf (Colobopsis), 3836
depressus (Mychocerus), 7
Derecyrta, 314
Dermestes, 228
Diceratucha, 185
Dictvrillus, 8
Dictynna, 296, 332
Dielocerus, 320
difficilis (Otiorrhynchus), 222
difformis (Cremastogaster), xxx
Diglottini, 245
dinochares (Deudorix), evii, ¢xxxii
Dinopsis, 242
Diphamorphos, 256, 257, 259, 294
333
Diploptera, cx
Diplotoma, 6, 17
Diprion, 289
Diptera, cxxxiv, exxxix
Dirce, 185
dirce (Gynaecia), xlv
Dirphya, exxxix, exli, exli
discipennis (Medon), 74
Discogenia, 48
Discoloma, 48
discrepans (Lecanium), 134
Disophrys, 93, 113
distincta (Pangonia), ev
distinctus (Pterygophorus), 291, 292
Ditoma, 6, 10, 11, 16
Ditomini, 10
divaricata (Perga), 269, 277, 283
divergens (Clarissa), 258, 294, 295,
300
diversipennis (Stigmatobracon), 92
diversor (Echthromorpha), 344
te
fi (Papilio),
2)
dohertyi (Delias), 121, 122, 123
(Huphina), 120, 123
i (Mimacraea), lix |
(Pieris), 121, 123
Dolerus, 324 |
dorsalis (Perga), 263, 267, 268,
330
doryca (Mynes), 126, 127, 128
dotata (Hydriomena), 186
doxo (Pieris), 193
», (Pinacopteryx), Ixxvi, 193
Drassidae, xevii
Drepanidae, 160, 189
Dromieca, xevili
Drosophila, xxii
Dryinidae, 340
dubia f. wahlbergi (Euralia), xxiii
5H (Hypolimnas), xxiii |
1, (Perga), 284
dubius mima (Euralia), xliii
ducissa (Teracolus), cii, evii, el, cli,
elii
Dudgeona, 156, 157
Duomitus, 162
Dynamine, ii
Dyspessa, 159
Echthromorpha, 344
edna (Neurochyta), 181
egina areca (Acraea), civ
Elateridae, cxxxiv
elatus (Pompilus), 340
;, (Psammochares), 340
elegans (Ipobracon), 104
,, (Torymus), clxiv
eliminata (Sarangesa), XXxv1
elion (Epitola), xxiv
elongatulus (Trogophloeus), 61
eluta (Exoprosopa), exxxvil
emma (Huphina), 119
», (Pieris), 119
encedon (Acraea), X, XV, XvVili, Xix,
; xlii, exill, exvill
f. daira (Acraea). x, xv, xviii,
xlii, exvili
f. infuscata (Acraea), x
f. lycia (Acraea), x, xvili,
xii
Encyrtinae, 341
Endromidae, 189
Endoxyla, 162
Epamera, 1xxix
epaphia (Glutophrissa),
elxxi, clxxii
Ephialtites, 321
Ephydridae, xxxv, xl
Eisomus, 213
erato (Heliconius), clii, elx, 347, 350,
>
2”
”
>
ell, ~chxx,
cXeVill
351, 352
)
erato albida (Heliconius), 350
amazona (Heliconius), iv, 352
”
», andremona (Heliconius), 350
», chestertoni (Heliconius), elx
;, colombina (Heliconius), clx,
elxi
»» constricta (Heliconius), 350
», extrema (Heliconius), clx
», magnifica (Heliconius), 352
ys molina (Heliconius), elxi
,, oberthueri (Heliconius), 351
phyllis (Heliconius), iv, v
,, f. tellus (Heliconius), eliii, 350
Eremocossus, 158
erikssoni (Dromica), xevii
5 (Myrmecoptera), xevii
Eriocampa, 257
Eriocampoides, 257
| Eriocranidae, 167
| Eriocrantidae, lili
‘eriphia (Herpaenia), ciii, elii
eris (Teracolus), lviii, cili, eli
erraticum (Tapinoma), ¢lvii
erycina (Castnia), elxiv, elxv
Erythrapion. 216
esenbeckii (Perga), 270
etesipe (Charaxes), Ixxxii, exx
ethalion (Charaxes), Ixxix, Ixxx,
Ixxxi, Ixxxiv
on f. rosae (Charaxes), lxxx,
lxxxi
5 f. m. swynnertoni (Char-
axes), [xxix
etheocles (Charaxes), lx, Ixxix, ]xxx,
)xxxili, exx, xxi, elxxvi
alladinis (Charaxes),
Ixxxiii
f. m. carpenteri (Charaxes),
Ixxxii, Ixxxiv
f. chanleri (Charaxes), 1xxxi
f. m. kirki (Charaxes),
Ixxxi, Ixxxii
f. manica (Charaxes), Ixxx,
exix, exxi, elxxvi, clxxvii
phaeus (Charaxes), Ix,
Ixxx, cxix, cxx, clxxvi,
elxxvil
m. regalis (Charaxes),
]xxXxii
m. rogersi (Charaxes),
Ixxxi, Ixxxil
f. virilis Charaxes), ]xxxiii,
]xxxiv
eucalypti (Perga), 267
7 (Phylacteophaga), 255
eucharis (Delias), 125, 127
», (Polynema), 341
Eucosma, 171
ti
”
fs
f,
fe
”?
(> exci.)
eugenia (Morpho), elxviii
»» f. damocles (Morpho), elxviti
Eumenidae, li, 338
Eumerus, ]xxvii
eumolpe (Delias), 125, 127
Eupithecia, clx
Euralia, xliii, xliv,
Euriinae, 257
euryades (Heliconius), 352
Euryopsis, 257, 258, 295, 332
Eurys, 257, 258, 259, 294, 295, 296,
297, 299, 300, 326, 332
eurytus (Pseudacraea), vii
euryxantha (Appias), 120, 122
Ls (Delias), 119, 122
ay (Huphina), 118, 120, 121,
1225 12351285129
ar (Pieris), 120, 122
5 (Tachyris), 119, 122
euryxanthe (Huphina), 118, 122
Eutermes, xcix
evagore (Teracolus), cli, clii
Evaniidae, 341
Evaniininae, 341
eyarne (Teracolus), cli
elxxii
- elatior (Catagramma), 11
aN excelsior (Catagramma), ii
a excelsissima (Catagramma),
ili
= michaeli (Catagramma), iil
ockendeni (Catagramma), 111
exiguus (Ancaeus), 58, 59
eximius (Sarothrias), 2, 8
expansum (Lecanium), 135
D var. quadratum
nium), 144
a5 (Paralecanium). 135, 136
expressa (Culama), 160
aa (Macrocyttara), 169
expulsus (Apanteles), 346
exsecta (Formica), Ixvi
extranea (Hyptiogaster), 342
faberensis (Myllaena), 244
fagella (Chimabacche), 173
falernaria (Monoctenia), 184
fasciata (Empusa), cbxiii
fasciatus (Hypomedon), 74
faunus f. albata (Oxylides), xlviii
fenestrata (Chromatophania), cxlvi
ferruginea (Perga), 264, 266, 272, 274,
277, 279, 285, 329
ferrugineus (Mychocerus), 7
af (Rhynchophorus), 225
festinata (Agathiella), 109, 111
festivus (Cyanopterus), 94
ficus (Pulvinaria), 144
fieldii (Colias), 116
(Leca-
fieldii chinensis (Colias), 116
fijiensis (Physcus), 341
», (Prosopis), 336
filipendulae (Zygaena), 177
fimbriventris (Megachile), 337
flaviceps (Ipobracon), 105, 106
3 subsp. mackayensis
bracon), 105
», (Poecilobracon), 105
flavipennis (Coproporus), 239
flavogattatum (Conosoma), 234
flavosignatus (Thyreopterus), ¢
floccifera (Pulvinaria), 1384, 146, 153
flora (Kunica), iv
florella (Catopsilia), cii, cli, clii
foedus (Eremocossus), 158
Foeninae, 342
foersteri (Perga), 265, 278, 285
forcipata (Bembex), exlvi
formicarii (Lecanium), 134
Formicidae, 334
fornasinii (Anthia), ¢
fortepunctatus (Stenus), 68
(Tesnus), 68
fossigerum (Cryptobium), 81
foveatum (Cryptobium), 81
foveatus (Cycloterinus), 217
fraterculus (Ipobracon), 105
Frenatae, 167
froggatti (Perga), 274
frugicola (Anotylus), 66
» (Oxytelus), 66
fryeri (Bothrideres), 2, 28
fuciformis (Hemaris), clv
fuliginosus (Acanthomyops), Xxxvii
(Donisthorpea), xxxvii
fulva ’(Andrena), Ixviil
fulvopilosus (Iphiaulax), 97
funerea (Delias), 127
furcata (Paracossus), 178
fusca (Formica), xxxvii
fusculum (Conosoma), 234
gallica (Polistes), xvi, xvii
gambiana (Ceria), ex
a (Cerioides), ex
gardineri (Cerylon), 2, 36, 48
a (Neotrichus), 2, 19
gaudialis (Pterygophorus), 290
Gazera, 175, 182
geoffroyi (Mynes),
127
ie f. doryea (Mynes), 124
yeometridae, 185, 187, 189
Geometrinae, 185, 189
gerda (Pinacopteryx), Ixxvi, 193, 196
197, 198, 199, 202, 203, 204, 206
207
Gerris, cxxxiv
(Ipo
18s alos os.
( ce.)
gidica (Relenois), Ixxxvi, cii, eviil,
exiv, cli, cli
gigantea (Pachytoma), exlvi
gilberti (Ipobracon), 104
Givira, 164, 165
glaber (Philomastix), 287, 288
glaberrimus (Acylophorus), 90
glabra (Perga), 275
» (Philomastix), 248, 265
glauca (Notonecta), ii
globulus (Mimocyptus), 241
Glossina, xcili, xclv, ¢V
Glyptolopus, 42
Glyptomorpha, exli, exlii
goetzius (Byblia), Ixxxv, cxiv
gracilis (Holonychus), 219
graeflei (Alastor), 339
, (Paralastor), 339
granadillae (Anotylus), 66
s (Oxytelus), 66
erandipennis (Mimodacne), ¢
granulatus (Hypomedon), 75
vravenhorstii (Perga), 277, 285
gregoryi (Ityraea), Ixxvill
gryllotalpa (Gryllotalpa), elxiii
guderiana (Charaxes), exix, xxi
guerinii (Perga), 273, 274, 284
guineesis (Dolichomutilla), xeviil
Gymnusini, 243
haematoda (Formica), 334
Pes (Odontomachus), 334—
haematodes (Odontomachus), 334
haemorrhoidalis (Liris), exxxix
er (Lis opimpla), 343
halidaii (Perga), 279, 330
» (Xyloperga), 279, 330
halimede (Teracolus), ciii
halophiloides (Taenosoma), 62
- (Trogophloeus), 62
halophilus (Trogophloeus), 62, 63, 65
Hamanumida, elxyxvil
hansali baringana (Charaxes), exx
harona (Oxypalpus), cil
Harpagomyia, XXxil, XXXliil, XXxXiv,
XXXV, XXXVi, XXXVil, xl
harpalyce (Delias), 125
harpax (Axiocerses), exxxii, ¢xxxill
hartigii (Perga), 276, 277
hauttecoeuri (Alaena), cxxxii
heeabe (Terias), cli
heldreichi (Glyphazus), elxiil
Heliconius, 351
helveticata var.
thecia), clix, elx
Hemipecten, 160
Hemiptera, exxxlv, cxxxix
hemisphaericum (Lecanium), 141, 143,
148
areeuthata (Eupi-
Hepialidae, hii, 167
Heptacola, 255, 264, 265, 275, 285
331, 332
Hesperidae, exxxiil
hesperidum (Coceus), 130, 145, 146,
147
ae (Leeanium), 153
Heteroglymma, 219, 222
Hibrildes, exxxiv
Himaeya, 162
hindei (Leucochitonea), cil
hintza (Castalius), cil
hippia (Nepheronia), 128
hirticornis (Imealia), 326
hobleyi (Pseudacraea), vii
Holocephala, 5
Holocerus, 159
Holonychus, 218
homeyeri (Spindasis), exxxii
hortensis (Pteronidea), 316
humanus (Pediculus), lvi, elvii
humeralis (Carpophilus), 224, 228
Huphina, 118, 120, 12], 1¥2, 128,
126
hyale ab. nigra (Colias), 116
hyalinus (Trichorhachus), 261
hyalites dannfelti (Amamris), cxvi
Hyblaea, 183
hybridana (Isotrias), 172
hydara (Heliconius), 352
Hylotoma, 254, 332
Hymenoptera, exxxix, 304, 307, 308,
309, 310
Hypoeyptus, 241
Hypolimuas, xliv
Hyponomeuta, exxxix
Hyponomeutinae, 173
Hypsidae, 188
iasis (Epamera), 1xxix
icarus (Polyommatus), 1
~Ichneumonidae, 343
Ichneumoninae, 345
Ichthyurus, exl
ignavum (Pison), 338
iltis (Delias), 125
imitator (Pseudacraea), ¢xxiv
immaculata (Echthromorpha), 344
immaculatum (Conosoma), 235
impressa (Evania), 342
impressicollis (Lispinus), 59
impura (Phragmatoecia), 161
inanis ( Volucella), xev
Incalia, 325, 327
inconspicua (Clarissa), 258, 300
a (Eurys), 258
inconspicuus (Clarissa), 295, 300
3 (Eurys), 295, 300
incretus (Teracolus), xcii, cli
{ ca)
indica (Zeuzera), 163
indicum (Calliderma), 78, 80, 81
indicus (T'rogophloeus), 61
Inermis (Stizus), 334, 337
inferna (Delias), 125, 126, 127
ingressor (Ipobracon), 102
Ingurimorpha, 164, 165, 178
innotatus (Cyanopterus), 94, 95
inquirendus (Pompilus), 340
insignis (Lterygophorus), 291,
293
insularis (Aphanocephalus), 2, 49, 57
(Valaminus), 71
intermedia (Cicindela), exliv, cxlvi
interposita (Alaena), exiii, exxxii
interruptus (Pterygophorus), 247, 291,
292, 293
intricans (Perga), 267
Iphiaulax, exli, 95
Ipobracon, 102
Iridopsis, Xxxi, XXxii
iris (Diestogyna), clxxvii
irma (Delias), 124, 125, 126
irpex (Psammochares), cxlv
irrorata (Anticarsia), 346
Isomerinthus, 222
Isotrias, 171
italicus (Caloptenus), clxiv
Ithycerus, 212, 225, 226
Ityraea, xxviii
jamesoni (Eagris), ¢xxxill
jobaea (Nepheronia), 128
», (Pareronia), 128
johanna (Alaena}, Ixxxvii
jucunda (Paraperga), 331
», (Perga), 280
judith (Huphina), 119
», Pieris), 119
Jugatae, 167
julus (Argiolaus), Ixxix
jurinei (Perga), 280
» (Xyloperga), 286
juvencus Se 311
(Sirex), 253, 311
=n (Urocerus), 311
Kalosysphinga, 313
kietleri (Pseudogonatopus), 340
kirbii (Perga), 268, 284
klugii (Perga), 268, 284
kraatzi (Astenus), 72
» Oxytelus), 66 —
kuenowi hypoxantha (Pseudacraea) vii
kummeri (Delias), 125
ladas (Delias), 119, 121, 122, 123, 128
»» (Huphina), 120, 123
laetus (Eurys), 258, 294, 295,
laevigatus (Miris), ii
laevinodis (Myrmica), clvii, clxviii
rls)
296
lalage (Perga), 281
», (Xyloperga), 286
laminatus (Camponotus), 335
Lamiidae, exl
Lampidinae, xlviii
| laon (Epamera), Ixxix
| lara (Delias), 128
Larentianae, 186
Larradomorpha, xii
Larridae, exxxix
Larrinae, 338
| Lascotonus, 6, 22
| Lasiocampa, 180, 181
_latreillei (Perga),
laura (Pteronymia), li
Lasiocampidae, 179,
185, 187, 189
180, 181, 184,
latec inetus (Hypomedon), 74
lateralis (Eulissus), 83
Lathrobium, 77
latibalteata (Agathiella), 109, 110
an (Agathis), 110
laticeps (Actobius), 86
latifrons (Palarus), xcix
276, 279, 286
lavinia lavinia (Pseudoseada), li
troetschi (Pseudoscada), |
9
| leachii (Perga), 279
,, (Pterygophorus), 292, 293
leaena (Platyagathis), 114
Lecaniinae, 135, 144, 145, 153
Lecanium, xxx, 133, 134, 135,
142, 148, 144, 145, 153
leda (Eronia), xeli, ¢xvii
Lentagena, 165, 178
leonidas (Papilio), exiil, exvi
leontopolitana (Pronomaea), 245
Lepidoptera, cxxxix, 155, 160, 166,
167, 169, 170,174, 189
Heteroneura, 166, 167,
168, 186, 187
nA Homoneura, 167
Leptothorax, cliii
leucocnemis (Oligolinus), 82
leucomelas (Perga), 275
Leucothyris, li
levissimus (Cyanopterus), 94
, (Iphiaulax), 94
levubu (Abantis), cii, ciii
lewisii (Perga), 263, 266,
274, 329
(Pseudoperga), 263,
330
libelluloides (Palpares), elxx
liliana (Belenois), 192, 193
(Pinacopteryx), lxxvi aoe 192,
193, 194; 195, 196, 197, 198,
199, 201, 202, 203, 204, 205,
206, 207
140
?
O72,
274,
a9
te]
( cen )
liliputanum (Cerylon), 2, 38, 48
limacina (Caliroa), 316, 332
Limacodidae, 166, 177, 178, 188, 187,
189
limnoria (Precis), ¢xxvi
NA f. taveta (Precis), cxxvi
linearis (Somoleptus), 82
linus (Gazera), 175
Liparidae, 182, 184, 187, 188, 189
Lipteninae, xlvili
Lispini, 58
Lispinus, 58
Lissopimpla, 344
littoralis (Taenosoma), 63
,, (Trogophloeus), 63
lituratus (Piezodorus), ii
Lixidae, 217
Lomechusa, XxXXV1i
Longicornia, CXXX1V
longipennis (Glossina), xlii
longius ‘Cerylon), 2, 32, 47, 48
longulum (Lecaniwm), 134
Lophocateres, 4
Lophyridinae, 257
Lophyrinae, 257, 304, 322, 323, 325
Lophyroides, 289
Lophyrus, 256, 289
lovendali (Cryptophagus), i
lucens (Hypomedon), 75
(Taenosoma), 63
,, (Trogophloeus), 63
lucida (Perga), 272
lucretia (Pseudacraea), vil
f. expansa (Pseudacraea),
exXiil
», lucretia (Pseudacraea), cxxiv
ludens (Milichia), xxxvii
lugubris (Ammophila), xcix, exxxv,
CXXXVI
lyaeus (Papilio), Ixxxv
Lycaenidae, xxiii, xlv, xlviii, Iviii,
exili, exxxii
Lycaeninae, xlvii, xlviii
Lycidae, exxxix, exl, exli, exlii
Lydidae, 304, 319
Lydini, 319, 320, 321
lyoneti (Cossodes), 156
Lyreus, 24
macaensis (Polistes), 339
5 (Vespa), 339
macaronius var, kolyvanensis (Ascala-
phus), clxx
macleayii (Heptacola), 265, 331
(Perga), 248, 287
(Philomastix),
287, 288, 331
Macrobracon, 96
Macrocyttara, 160, 168, 186
mn
9?
”)
2?
248, 265,
maculatus (Camponotus), xxix
madagascariensis (Montoma), 2, 5
magnifica (Paraclara), ¢xxxix
major (Nabis), li
maligna (Agathiella), 109, 111, 112
mangiferae (Phenacoceus), 130, 147
Mantidae, exxxiv
marginalis (Dytiscus), elvii, clxi
marginatus (Ipobracon), 102
marshalli (Chlamys), ¢xxxViil
(Mimacraea), xv, Xvili, xix,
9 5
ix
3 race dohertyi (Mimacraea),
XV
marsupiale (Lecanium), 134
marsyas (Thecla), xlv
martialis (Microdus), 106, 108
maura (Xuthia), 12
mayrii (Perga), 270, 271, 330
5, (Plagioperga), 330
Mecedanum, 2, 7, 28
Mecoptera, 167
medianus (Merinotus), 99
mediocinctus (Leionotus), 359
: (Odynerus), 3839
Megachilinae, 336
megaera (Pararge), lv
ab. mediolugens
clili
Megalodontoidea, 304, 319
Megalommum, 97
Megaponera, xc
megapterus (Iphiaulax), 97
Megarthropsini, 231
Megarthropsis, 231
Megarthrus, 231
melanacrias (Pseudogonatopus), 340
melanarius (Coproporus), 239, 240
melittae (Stylops), xxii, lxxiii
mellifica var. adansoni (Apis), xcix
Melolonthidae, exxxiv
melpomene (Heliconius), clii, 347, 348,
350, 351, 352
aglaope (Heliconius), 349,
a (Pararge),
99
352
a amandus (Heliconius), 350
- cybele (Heliconius), 348,
349, 350, 351
Ps », ab. cybeleia (Heli-
conlus), 349
a » ab. faustalia (Heli-
conius), 348, 349
a », ab. faustina (Heli-
conius), 3850
3 » ab. funebris (Heli-
conius), 351
2 », ab. negroida (Heli-
conlus), 348, 349
(
cecil
)
melpomene galanthus(Heliconius), 348 | misippus f. inaria (Hypolimnas), v, x,
. hermogenes (Heliconius),
348
A ab. melpina (Heliconius),
348
5 melpomene ab. compacta
(Heliconius),
348, 349
At -" ab. faivrel
(Heliconius),
348, 349
7 5 ab. mela-
nippe (Heli-
conius), 349
a nanna (Heliconius), iv, v
9 ab. penelope (Heliconius),
348, 350
» «* ab. rufolimbata (Heli-
conius), 348
a thelxiope (Heliconius), iv,
348, 351, 352
a5 5, ab, aglaopeia (Heli-
conius), 349, 350
a », ab.negroidens(Heli-
conlus), 348, 349
a Te tO rufolimbata
(Heliconius), 349 |
+ » ab. stygianus (Heli- |
conius), 351
ar ab. timareta (Heliconius),
348
3 ab. vicinus (Heliconius),
348, 350
mendosa (Orgyia), 182
meridioualis (Agathiella), 109, 110
Merinotus, exli, 98, 99
mesentina (Belenois), ciil, clii
metallica (Eurys), 294
», (Neoeurys), 297, 298, 299
Miacora, 158
Microceridae, 214
Microcerus, 215
Microdus, 106
Microgasterinae, 346
Microlepidoptera, 174
Micropterygidae, liii, 167
Milichia, xxxiii, xxxvii, xl
Mimacraea, lix
mimeticus (Lycidocoris), cxxxix
Mimocyptus, 241
minima (Agathiella’, 109, 113
minimus (Coproporus), 240
minor (Diphamorphos), 294
minutus (Lispinus), 60
miranda (Epitola), xlvili, xciil
misippus (Hypolimnas), v, vi, vil, vill,
rep oS ody oabbin >. qyno.4 At
XVlil, xxi
X15) X15 EXLV ys KV IUlls exp
xhi
moesa (Argiolaus), lxxix
Molippa, 117
Monoctenia, 185
Monoctenianae, 185
Monotoma, 4, 5
Monotomidae, 2, 4
monstruosus (Cautomus), 42
monticola (Conosoma), 238
morsitans (Glossina), xcv
motozi (Sarangesa), XxXVil
motozioides (Sarangesa), ¢xxxiii
multistrigata (Zeuzera), 163
mutator (Belonuchus), 88
(Bracon), 100
”?
. (Campyloneurus), 99, 100
7 (Ichneumon), 100
Mutilla, xevii, 328
Mutillidae, xevili
Mychocerus, 7, 45
Myllaenini, 244
Mymarinae, 341
Mynes, 120, 123, 126, 128
Myosoma, 100
Myrmecinae, 335
Myrmeleonidae, cxxxiv
mysis (Delias), 125, 128
nancarrowi (Philomastix), 287, 288
nanna (Heliconius), 350
naraka (Nepheronia), 128
narcissus (Agrias), lviil
natalica (Acraea), civ, cxiv
natoliae (Saga), cl xiii
Naupactus, 213
neanthes (Charaxes), eviil
Nematinae, 323
Nemophora, 172
Neoeurys, 258, 259, 295,
298, 333
Neoperga, 330
Neotrichus, 6, 19
Nepheronia, 128
Nepidae, elxvi
nerissa (Huphina), 120
neumanni (Dromica), xevili
x (Myrmecoptera), xevili
Neurochyta, 181
Neuroptera, clxx
cs Planipennia, 167
newmanni (Perga), 264, 274, 279, 285
niavius (Amauris), vill
dominicanus (Amauris), ¢lxxii
296, 297,
”?
niger (Scopaeus), 77
nigrescens (Diphamorphos), 294
nigricans (Thinocharis), 73
-nigricornis (Dirphya), cxl, exli
(. ceiv )
nigricornis (Nitocris), exl, exli
nigrina (Delias), 125, 127
nigroaenea (Andrena), Ix xiii
nigrocincta (Ityraea), 1xxvili
nigromaculatum (Conosoma), 237
nigrum (Lecanium), 134
5, (Leucocraspedum), 243
nitens (Calliderma), 79
», (KEuryopsis), 258, 295
nitidicollis (Penthelispa), 10
nitidulus (Scopaeus), 77
nitidum (Cerylon), 2, 30, 48
nitidus (Eurys), 258, 295, 297
,, (Holotrochus), 68
5, (Parascopaens), 76
», (Trichorhachus), 259, 260, 261
-» (Trogophloeus), 64
Nitocris, exxxix, exli
nobilis (Holocerus), 158
s, (Macrobracon), 96
Noctuidae, 182, 183, 184, 187, 188
Nomada, Ixviii
norax (Cossula), 160
»» (Hibrildes), cxxxiv
Nosymna, 173
notabilis (Pinophilus), 70
Notiophygidae, 2, 48
Notiophygus, 48
Notodontidae, 182, 184, 187, 188
nubica (Anthophora), ci
nuda (Cardiocondyla), 335
nudaridia (Lentagena), 165
nudus (Leptothorax), 335
numenes (Charaxes), lxxxiii
Nymphalidae, cxvii
Nymphalinae, cxiii, exviii, exxiii, 123
Oberea, exlii
obliqua (Stilicopsis), 72, 73
obscura (Rhabdoenemis),
225, 227, 228
obscurus (Anotylus), 67
- (Oxytelus), 67
obtusiventris (Xiphydria), 253
oceanica (Colobopsis), 336
Rs (Pheidole), 335
oceanicum (Rhopalum), 337
oceanicus (Camponotus), 336
(Colobopsis), 336
(Crabro), 337
a (Rhopalum), 337
ochroptera (Mesoplatys), exlviii
octavia (Precis), ¢XXiv, CXxXvll, CXXVvill,
CXXX, CXxxii, c]xxvii
octavia (Precis), e])xxviii
223, 224,
>
”
>
» f. sesamus (Precis), cxxvii,
CXXVili, Cxxx, ¢elxxviii
» f. natalensis (Precis), cxxiv,
CXXVil, CXXVill, CXXx
—
odyssia (Huphina), 121, 122
oleagina (Cuissostages), 174
omphale (Teracolus), exiv
oncaea (Acraea), ¢xiv
onias (Dynamine), iv
opaculus (Paniseus), 345
Ophioninae, 344
Ophrynopus, 251, 252, 259, 317, 318,
328, 332
orbona (Pinacopteryx), 192
Orgiloneura, 113
orientalis (Astenus), 71
(Blatta), clvii
¥ (Trogophloeus), 61
ornythion (Huphina), 118, 123
ornytion (Delias), 119, 121 122, 123,
124,125, 126, 127, 128
(Huphina), 118, 120, 123
45 (Pieris),‘121, 123 :
Oryssidae, 251, 310, 314, 315, 318,
320, 321, 328
Oryssus, 309, 310, 317, 332
Osorii, 68
Ostomidae, 2, 3
Ostominae, 4
ovalauensis (Discolia), 340
(Eumenes), 338
a3 (Scolia), 340
oxyacanthae (Pulvinaria), 146
Oxylides, xlviii
Oxyteli, 61
Pachyeephala, 5
Pachylosticta, 327
Pachylota, 302
pacificus (Ooenocyrtus), 341
eS (Stizus), 337
Paederini, 71
Palaeorhiza, 336
pallida (Teriomima), xeii
pallidicolor (Ipobracon),
104
pallidipes (Glossina), xlii
palpalis (Merinotus), 99
Pamphilidae, 288
Pamphilinae, 320, 321, 327
Pamphilius, 309, 312, 313, 314
paneperata (Argiolaus), lxxix
Pangonia, civ, cv
Pangoniinae, cv
panthona (Cyclosia), 176
paphia (Dryas), exiv
», f. valesina (Dryas), cxv
Papilio, xlii
Papilioninae, exiv, exvi
Paracossus, 156, 177, 178
parallelocollis (Neotrichus), 2, 21
Paralyreus, 6, 24
Paraperga, 330
+e)
9
9
102, 103,
( ecev )
Parascopaeus, 76
Pareronia, 128
parsimon (Catochrysops), Ixxix
parummaculata (Aspidomorpha),
exlviil
parva (Paracossus), 178
parvipuncta (Phragmatoecia), 160, 161
parvulus (Coproporus), 240
A (Somoleptus), &2
parvus (Holisus), 85
», (Oligolinus), 81
», (Palaminus), 71
pastazza (Catagramma), i1, iil
excelsa (Catagramma), ili
pastazza ab. speciosa (Cata-
gramma), ii
Paururus, 253
pechueli (Crenis), exiii, exxii
pectinea (Incurvaria), 173
pedunculatus (Microdus), 106
peletieri (Perga), 285
pellucida (Dioptis), 1, li
pelopia (Castnia), elxiv, clxv
pelopioides (Castnia), clxiv
Pemphredon, 311
Pentatoma, ii
Penthelispa, 6, 9
Perga, lvi, lviii, 248,
255, 256, 259, 261,
265, 266, 267, 272,
289, 323, 324, 325,
330, 331, 332
Pergadopsis, 330
Pergidae, 258, 288
Pergula, 256, 259, 288
perparvulum (Cerylon), 2, 33, 48
perpessicius (Halictus), 336
perpetua (Dynamine), iv
perplexum (Conosoma), 237
Perreyia, 257, 289, 326
Perreyiidae, 253
persephone (Delias), 122, 123
i (Huphina), 121, 123
persicae (Lecanium), 134
», (Pulvinaria), 146
persimilis (Stilicopsis), 72
perspicilla (Arrhenophanes), 174
pertinax (Anobium), lv
pertusa (Sarangesa), Xxcil
petiverana (Tirumala), exvi
petraea (Acraea), Ixxxv
phaleros (Thecla), xlv
Phaneromeris, cx]
phasma (Catochrysops), lxxix
Pheidole, xxxvi
Phenacopergini, 323
phileris (Belenois), clxxi
(Pieris), elxxi
be)
9
250, 253,
263, 264,
287, 288,
327, 329,
92
Philomastix, 248, 253, 256, 259, 265,
287, 288, 320, 326, 327, 331, 332
phlaeas ab. intermedia (Rumicia), cliii
phlegyas (‘Teracolus), Ixxxvii
phocaea (Nepheronia), 128
phoenicis (Rhynchophorus), 223
Phragmatoecia, 160, 161, 162, 163
Phrissura, ¢iii
Phtheochroa, 160
Phylacteophaga, 248, 253, 255, 259,
BYIO, BYia BBY)
Phylotoma, 313
Phytaecinae, ex], exlii
piceus (Hydrophilus), elxi
picta (Belenois), lix, lxxxvii
Pieridae, 118
Pierinae, Ixxxvi, cii, exii, exiii, exiv,
CXxv, exvil, clii, 119, 123
Pieris, clxxi, 119, 120, 122)
pierus (Aloeides), Ixxxvili
Piezia, xevii
pigea (Pinacopteryx), Ixxv, 191, 192,
195, 196
Pimplinae, 343
Pinacopteryx,
208
pingasa (Nepheronia), 128
piniarius (Bupalus), 185
Pinophili, 70
Pissodes, 210, 216, 217, 223
Plagioperga, 330
planatus (Liatongus), exlvii
Platyagathis, 113
Platypidae, 211, 213
Platypus, 217, 227
Plebeinae, xlviii
plistonicus (Sarangesa), xxvii
plumbeus (Polycleis), 218, 222
poggei (Pseudacraea), v, vi, vii, viii
DAEs Sly oil, MAA oop
128, 191
191, 192, 193, 195,
XVIy, VAT) RVI RIX, Xe
ei) Cxih, CXill, CxxU, xxiv,
elxxvii
f. carpenteri (Pseudacraea), ix,
Kon Rls Elly RLV) ove XVI
exli, CXXill
policenes (Papilio), exvi
polioplaga (Xyleutes), 161
Polistes, Ixvii
polita (Perga), 263, 269, 276,
283, 329
(Pseudoperga), 263, 329, 330
», (Shoguna), 2, 5
Polycleis, 218
Polyclonus, 257, 259, 325, 33:
Polyhirma, xevili
polymnia (Mechanitis), clxix
Polyrhachis, li
9
247,
29
( covi )
pomonella (Carpocaypsa), 17]
Pompilidae, cxxxv, exxxviii
Ponerinae, 334
posthumus (Epitola), xxiii, xxiv, xxv,
XXvi
praeclarus (Campyloneurus), 99, 101
praepotens (Campyloneurus), 99, 101
Precis, lix, Ixxxvii, evi, cxxiv, cxxvii,
CXXVill, CXxx
princeps (Oedematopoda), exxxix
Procris, 177
profiseator (Bracon), 94
(Cyanopterus), 94, 95
ab (Ichneumon), 94
profugus (Campyloneurus), 99, 100,
101
9
Promachus, exxxvii
promissorius (Kuichneumon), 345
rp (Ichneumon), 345
Pronomaeini, 245
pronuba (Agrotis), 182
Prosopidinae, 336
Prosopis, 336
Prosthesima, xevii
Protocossidae, 186, 187, 188
Protopulvinaria, 143
Psammocharidae, 334, 340
Pseudacraea, v, vii, x, xi, xvi, cxiii,
exxili
Pseudobracon, exli
Pseudococeus, 132, 147
pseudolycia astrigera (Acraea), civ
Pseudoperga, 263, 274, 329, 330, 332
Pseudoscada, li
Pseudosirex, 321
psidii (Lecanium), 134
», (Pulvinaria), 130, 131, 132,
139, 140, 141, 142, 143,
144, 145, 146, 147, 148,
AOL VSO Fo 52. 153
33 ficus (Pulvinaria), 144
6 philippina (Pulvinaria), 144
Psithyrus, 283
psyche (Dicopus), 341
Psychidae, 164, 166, 178, 183, 187,
189
psyttalea (Amauris), xlii
Pteronus, 289
Pterygophorus, 248, 249, 250, 256,
257, 259, 289; 325,327, 882; 833
Ptilomacra, 157
pulchellus (Diochus), 84
pulcher (Oxytelus), 66
Pulvinaria, 134, 140, 143, 145, 146,
153
purpurea (Dromica), xeviii
pusillus (Lophocateres), 2, 3, 4
»» (Peltis), 4
Pycnomerini, 9
Pycnomerus, 6, 9
pygmaeus (Oxytelus), 67
pylades angolanus (Cosmodesmus),
exvil
" “a (Papilio), exvii
Pyralidae, 166, 179, 187
quadricolor (Ipobracon), 103, 104
quadiiplagiatus (Aphanocephalus), 2
D2EOG
Quediini, 90
queenslandensis (Oryssus), 252
quercus (Kermes), clix
(Lasiocampa), 180
3 (Zephyrus), |
quodi (Odynerus), 339
radiatella (Cerostoma), 173
rechingeri (Pison), 338
regalis (Cicindela), exliv
regina (Teracolus),evii, exvii, cli
regularis (Terias), exvii, cl, cli, clii
repanda (Coccinella), 224, 228
Rethona, 159
retiaria (Notogonia), 338
reticulata (Alaena), Ixxxvii, exxxiii
o (Telipna), cxxxili
Rhina, 217
Rhopalocampta, xxvii
Rhopalocera, 188
Rhynchitidae, 214
Rhynchophora, 209, 210, 211, 213,
214, 215, 216, 217, 218,219
Rhynchophorus, 212, 225, 227
Rhynchopsilopa, xxxv, xl
ribesiae (Pulvinaria), 146
riparia (Labidura), elxiii
ritsemei (Perga), 284
robiniae (Xystus), 158
robustum (Conosoma), 233
rogersi (Teracolus), Ixxxvii, cli, clii
rostrata (Pronomaea), 245
rostratus (Lycus), exxxix
rotundicollis (Acylophorus), 90
rubicundus (Medon), 73
rubripes (Perga), 278
rudis (Pollenia), xxiii
ruficeps (Agathiella), 109, 110, 111
rufina (Xuthia), 12
rufipes (Chelonus), 346
(Pentatoma), ii
(Rhynchium), 338
», (Vespa), 338
rufithorax (Microdus), 106, 107, 108,
113
rufiventris (Coproporus), 238
rufobrunnea (Adinopsis), 243
rufobrunneum (Conosoma), 234
99
99
Le)
/ rufobrunneus (Microdus), 106
(
rufomaculata (Perga), 280
rufotestaceum (Conosoma), 23
rufotestaceus (Taenosoma), 64
‘ (Trogophloeus), 64
rufum (Calliderma), 78, 79
rufus (Cyanopterus), 94, 95
a (Iphiaulax), 95
rugicolle (Calliderma), 80
ruginodis (Myrmica), eliii
rugosa (Agathiella), 109, 112
rugosus (Nabis), 1
rutilans (Kurys), 296
saba var. epaphia (Pieris), clxxii
sor UY PICA (Pieris), celxxii
sabina (Molippa), 117
a CE brissura); clxxeiclxxa
sabulosa (Stenocyttara), 164
Saga, clxiii
salicis (Pulvinaria), 146
sanguinolentus (Elater), cliii
2 (Philonthus), 87
Sarangesa, XXV1, XXvii, xcii, exxxili
Sarothrias, 6, 7
2
238
6
saturnus (Charaxes), Ixxxi, ]xxxii,
CX1x, CXXi
satyrata (Eupithecia), clx
Satyrinae, cxxxii
scabrinodis (Myrmica), clvi, clvii,
elxvili
Schausiana, 160
schillingi (Chorosoma), ii
schiddtei (Perga), 267, 284
Bchizocera, 325
Schizocerides, 259, 260
schmeltzii (Camponotus), 335
Schoenobius, 179
Scoliidae, exxxviii, 840
Scoliinae, 340
Scolytidae, 209, 210, 211, 219, 220
Scopaeus, 76
scotti (Cicones), 2, 6 12
(Lascotonus) 2, 22, 33, 47
-, (Paralyreus), 2, "O4, 20, 445
seul pticollis (Thyroderus), 2, od, 41
44, 45, 47
scutellaris (Oberea), exlii
scutellata (Cerealces), 255, 287
7 (Megachile), 337
sellata (Perga), 274, 285
semipunctata (Lissopimpla), 343
Pr (Rhyssa), 343
semipurpurata (Xyloperga), 280, 281
var. melanaspis (Xylo-
perga). 281
semire (Pseudacraea), vii
senegalensis (Terias), el, clii
senex (Ptilomacra), 157
sericatus (Ophrynopus), 252
99
3)
cevil
)
sericea (Perga), 274, 284
servillei (Pseudobracon), cxl
sesamus (Precis), xxvii, lix
Sesia, xxix
Sessiliventres, 308
setosus (Lispinus), 59
severina (Belenois), Ilviii, Ixxxiv,
Ixxxvi, cii, cili, exiv, cli, clii
Shoguna, 4, 5
siamensis (Trogophloeus), 61.
sicana (Xuthia), 2, 6, 12, 24, 33, 47
Sigalphogastra, 99
signaticornis (Actobius), 86
silarus (Argiolaus), 1x, cil
silvestris (Trogophloeus), 61
simana (Pieris), 198
simana (Pinacopter yx), Ixxv, cili, cvi,
eviii, exii, exiii, clii, 198, 194, 195,
196, 197, 198, 199, 201, 205, 206,
207
similis (Dirphya), exl, exli
(Megachile), 337
jou CNitocris)5,.cxl, ix
simillima (Molippa), 117
simonsi (Henotesia), evil, ¢xxxil
singularis (Ancaeus), 58
(Colobicones), 2, 16
5 (Tyrtaeus), 2, 26
sinuata (Nemoptera), clxx
Sirex, 258, 259, 303, 309,
332
Siricidae, 252, 307, 309, 311, 312,
317, 318, 319, 320, 321, 328
sisyrota (Titanomis), 173
Sitones, 217
skoptoles (Mimacraea), xix
smithu (Perga), 273, 274
sobrinus (Trichorhachus), 261
sophia (Synemon), 175
speciosa (Ityraea), Ixxvili
specularis (Lispinus), 59
Sphegidae, xcix, 337
Sphenophorides, 214
Sphongophorus, xlix
29
9
Bis 328)
313,
_ spilleri (Pinacopteryx), 192
spinolae (Perga), 276
splendens (Harpagomyia),
XXXVHi
spumarius (Philaenus), cli
Staphylinini, 85
Stegomyia, XXX, XXX1, XXXIil, XXxvi
clxxvi
Stenini, 68
Stenocyttara, 164
Stigmatobracon, 91
Stizinae, 337
stolli (Delias), 125
striaticollis (Aphelotoma),
O.O.6
328
( eeviil
striatum (Anobium), lvii
strigatus (Eumerus), lxxvil
strigillata (Xylotrypa), 162
Stromboceros, 322
Stygia, 159, 178
Stylops, lxix, lxx, Ixxi, Ixxii, ]xxiii,
lxxiv, lxxv
suave (Conosoma), 237
subapterus (Coranus), i
subdepressus (Aphanocephalus), 2, 53,
56, 57
subfasciatus (Teracolus), cl
subglobosa (Caenocara), 1
successor (Iphiaulax), 97
suleatus (Philonthus), 87
sulcinodis (Myrmica), elvii
sulphurifer (Nanpactus), 216
Susica, 177, 178
swammerdamella (Nemophora), 172
swynnertoni (Charaxes), Ixxx, Ixxxi
sylvestris (Vespa), 311
Symphyta, 308
Synchloe, exlix
Synemon, 175, 176
synestalmenus (Sarangesa), Xcli
Syntomidae, 188
Syzygonia, 324, 325,
Syzygoniides, 323, 32
Tabanus, civ
Tachinidae, exxxix
Tachinus, 241
Tachyporini, 233
Tachyris, 118, 119, 120, 122
tahitense (Pison), 338
takosama (Aloeides), Ixxxvii, 1xxxvili
tales pythagoras (Eueides), iv
tantillum (Cerylon), 2, 35, 48
tarquinia (Pseudacraea), Ixxxv
tasmanica (Neoeurys), 298
Telephoridae, exl
telicanus (Tarucus), exili
Temnochilinae, 3
tenebricosa (Timarcha), Ixxvii
Tenthredella, 324
Tenthredinidae, exxxix, 252, 262,
306, 311, 312, 318, 314, 315, 327,
318, 319, 320, 321, 323, 326, 332
Tenthredinoidea, 308
Tenthredo, 311, 322
tenuicornis (Myllaena), 244
tenuissima (Agathiella), 109, 111
Teracolus, Ixxxvii, c¢lil, cvi,
exvil
Terias, exvii, cl
Termites, xcix
termitiformis (Shoguna), 5
terra (Pseudacraea), vii
tessellatum (Xestobium), lvii
326, 327
i
exii,
)
testaceipennis (Diglotta), 245
testaceus (Apioderus), 65
tetragrammicus (Formicaleo), clxx
Tetramorium, clyii
Theclinae, xlviii
Theronia, 344
Thione, 5
thoracica (Clarissa), 258, 295, 300
Thyatiridae, 184, 187
Thynnidae, 306, 326
Thyroderus, 7, 44
tibialis (Pteronidea), 316
tigrata (Acyttara), 165
timon (Tanuetheira), xxix
Tineidae, exxxix, 166, 172, 173, 186
tiridates (Charaxes), Ixxxiii
Titanomis, 173, 186
tityus (Hemaris), clv
tomentosa (Pulvinaria), 134
torresensis (Stigmatobracon), 91, 93
torridus (Ipobracon), 104
Tortricidae, 166, 171, 172, 186
Morbrix, sls Wie 5
Toxorhynchites, xxxill, XXXVi, XXX1Xx,
x] :
trabeatus (Chlamydolycus), ci
3 (Lycus), ci
transieus (Iphiaulax), 95
Trichopteryx, 48
Trichorhachides, 260
Trichorhachus, 254, 259, 260, 325,
332
trichorostris (Harpagomyia), Xxxxiis
xl
tricolor (Agathiella), 109, 110, 113
tridens (Stizus), 337
Trigena, 165
Trigonops, 219, 222
trigrammus (Myrmecaelurus), clxx
trimenii (Pseudacraea), exxiv
| trimmerana (Andrena), ]xxi
| trinotata (Stilicopsis), 72
| Trionus, 11
tristani (Lentagena), 165
tristis (Givira), 164
tritaea (Nepheronia), 128
tropicus (Lophyroides), 326
», (Perreyia), 326
Trypoxylon, exlvili
‘| Trypoxyloninae, 338
tuberculatus (Eumerus), xxvii
turneri (Henicospilus), 344
(Pergula), 256, 288
3)
», (Pterygophorus), 292, 293
», (Zenarge), 254
turrigera (Laccoptera), exlviil
Tyrtaeus, 6, 7, 26
ulula (Dyspessa), 159
( xcerx |)
umbonata (Pheidole), 335
uncinatus (Onitis), exliv
undulosa (Bhima), 180
unicolor (Oryssus), 318
uniformis (Pterygophorus), 290, 293
unimaculata (Agathiella), 109, 111
univittata (Perga), 264, 279
y (Xyloperga), 286
urania (Epitola), xxiii, xxv, xxvi
urinator (Bracon), 93, 94
uroceriformis (Sesia), XXix
urogaster (Ajianteles), 346
urticae (Aglais), clxxviii
usambara (Euralia), xxii
vacillans (Perga), 272
vaillantina (Egybolis). xxvii
valeria (Nepheronia), 128
vaniha vanilia (Hypoleria), 1, li
», vVaniliana (Hypoleria), |
varanes vologeses (Charaxes), ¢Xix,
CXX1
variegana (Kucosma), 171
variegata (Clania), 179
varilineatus (Probolus), 345
veitchi (Crabro), 337
» (Lissopimpla), 343
venata (Pinacopteryx), Ixxvi, 193, 194,
195, 197, 198, 199, 201, 205, 206,
207
venatus (Ixias), 194
venosa (Hibrildes), exxxiv
ventralis (Oberea), exlii
(Perga), 273, 274, 329
aS (Pseudoperga), 273, 274, 329
Vespa, xlvi
Vespidae, 339
vesta erato (Heliconius), 351
viridana (Tortrix), 171
viride (Coccus), 136, 137, 148, 149
(Lecanium), 134, 136, 137, 141,
VAS SAO HO, Lol Lb2. oo
99
3?
viridis (Coccus), 130, 131, 132, 133, |
134, 135, 136, 138, 139, 140, 141,
142, 144, 145, 146, 147, 148
vitiensis (Chelonus), 345
PROC. ENT. SOC. LOND., v. 1918.’
vitiensis (Cyphononyx), 334, 340
(Haplogonatopus), 340
i (Neogonatopus), 341
vitis (Pulvinaria), 184, 146
vittata (Saga), clxiii
| vitticollis (Oxythyrea), exlviii
vollenhovii (Perga), 284
Volucella, xev
| w-album (Strymon), 1
| - (Thecla), xlvi
walkeri (Bracon), 93
»5 (Conosoma), 236
walkerii (Perga), 265
wilkella (Andrena), Ixxiii, Ixxiv
wilkellae (Stylops), [xxii
xanthocephalus (Merinotus), 98
| Xantholinini, 81
| xanthopsis (Microdus), 106, 107, 108
xanthostigma (Stigmatobracon), 91,
92, 93
Xenandria, clxiv
Xenogenes, 185
xenopis (Diceratucha), 184
| Xiphydria, 253, 259, 303, 314, 328,
333
| Xuthia, 6, 11, 12
Xyleutes, 162, 163, 174, 186
| Xyloperga, 250, 253, 255, 259,
262; 263,264, 265,027.55) 2/9)
285, 286, 325, 326, 327, 350;
332
Xylotrypa, 162, 163
Xystus, 158, 186
Yphthima, exxxii
yvani (Ostoma), 4
5, (Peltis), 4
| Zenarge, 248, 254, 259, 324, 325, 333
zetes (Acraea), Cxli, eXvili ;
acara (Acraea), Civ, CX, exviii,
CXX1V
Zeuzera, 162, 163, 164, 186, 188
Zeuzeridae, 175
zonalis (Pterygophorus), 292
zoolina (Charaxes), evil
| Zygaena, 176
|
|
|
”
Eb)
oO
(. "eG -e8)
ERRATA.
TRANSACTIONS.
Page'185, description of text figure 55, for pintarus read piniarius.
Page 228, line 2 from bottom, for Dermest?s read Dermestes.
PROCEEDINGS.
Page Ixxxvii, 1. 7, for johanna read johannae.
Page exiv, 1. 15, for cleodava read cleodora.
Page exxiii, 1. i8, for only slightly yellowish read not quite so yellowish.
Page exlii, line 8, for Braconid read Braconoid.
Page cli, line 13 from bottom, for evagone read evagore.
Page clxvii, 1. 16, for C. W. Farquharson read C. O. Farquharson,
TRANSACTIONS.
Page 224, line 8 from bottom, for flavogattatum, n.sp., ead flavo-
guttatum, n. sp.
Page 241, line 3 from bottom, for Mimocyplus read Mimocyptus.
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