MUSTRALIA
Butterfly & C)ther Invertebrates C lub
Magazine of the
1326-0006
ISSN
/[www.bo
SEPTEMBER 2009
Price $6.00
DATE
54
ISSUE NO
ic.org.au
http
PLANNING AND ORGANIZING COMMITTEE 2009
President:
Vice President:
Treasurer:
Secretary:
Newsletter:
Publicity & Library:
Excursion Convenor:
Ross Kendall 07 3378 1187
John Moss 07 3245 2997
Rob MacSloy 07 3824 4348
Peter Hendry 07 3206 0048
Daphne Bowden (daphne.bowden1 @bigpond.com)07 3396 6334
Lois Hughes 07 3206 6229
Alisha Steward 07 3275 1186
PLANNING AND ORGANIZATION MEETINGS
A quarterly meeting is scheduled in order to plan club activities and the magazine.
See BOIC Programme.
CONTACT ADDRESS AND MEMBERSHIP DETAILS
PO Box 2113, Runcorn, Queensland 4113
Membership fees are $25 for individuals, schools and organizations
AIMS OF ORGANIZATION
e To establish a network of people growing butterfly host plants;
e To hold information meetings about invertebrates;
e To organize excursions around the theme of invertebrates e.g. butterflies, native
bees, ants, dragonflies, beetles, freshwater habitats, and others;
e To promote the conservation of the invertebrate habitat;
e To promote the keeping of invertebrates as alternative pets;
e To promote research into invertebrates;
e To encourage the construction of invertebrate friendly habitats in urban areas.
MAGAZINE DEADLINES
If you want to submit an item for publication the following deadlines apply:
March issue — February 21° June issue — May 21°
September issue — August 21° December issue — November 21°
Paropsisterna sexpustulata - Painting by Lois Hughes. Prints of this painting may be
available from the artist. Ph. 07 3206 6229
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 2
FROM THE PRESIDENT
The seasons seem to come and go at a faster rate as we grow older but at the time of
writing this report (August 23") we appear to have had an even shorter winter here in
Southeast Queensland with temperatures that are well above average this week. The
insects seem to believe that winter is over as the first Bottle Cicadas are calling 1n the
late afternoon, Meadow Argus, Chequered Swallowtails, Blue Triangles, Lemon
Migrants, Evening Browns and numerous small blues are on the wing while Common
Crows, that have been present for months, have decided to commence laying eggs.
Sugar ants have commenced nightly patrols and Polyrachis ants have started scouting
away from their leaf shelters. Of course, there is still scope for winter to return in the
coming weeks.....
In the middle of last year, Lois Hughes found a small beetle with red spots and
decided she would like to paint it for a “cover story” in Metamorphosis Australia.
Richard Zietek and John Moss were given the task of producing the story. Over a
year later and after much research and consultation, the final results are published in
this edition. It was worth the wait to read the text and to see Lois’ painting and the
images by Peter Hendry and Russel Denton.
Many thanks to all the other contributors who will forgive me for making special
mention of Murdoch De Baar’s article on Jewel Beetles and Wesley Jenkinson’s
report on his detailed observations of the life cycles of two species of Grass-darts.
Enjoy. Best wishes Ross
Creature Feature - An introduction to Paropsine Leaf Beetles... eeeccceeeeeeeeeees 4
An interesting record of the Hawkmoth (Macroglossum prometheus lineatum)........ 10
Jewel Beetles (Coleoptera:Buprestidae) : some viewS and Notes .............ccceseecceeeeeeeees 12
Life History Notes on the Narrow-brand Grass-att ...............cccccccssecccesseeeceeeceeeeeeeees 16
The Flame Flatwing (Austroargiolestes AMADLIL) ....ccccccccccesccccussccccsesccccaeccenenececaaeeceees 20
4" Biannual Moth Meeting - Canberra 2009 ........ccccccccecsecessecessecesseceececeesecececsceecseeees 21
Cuckoo Wasps (Hymenoptera : Chrysididae) .............cccccssececceseccceeseceeeescceeeeeceeeeeceeees 22
At The Light Trap - The Return of the Crambidae.......... ccc ecccccessecceceeeeceeeeeeeceeees 23
Book Reviews - Moths of Victoria - Part 2.00... ccccccccssccccesecccesececeeecceeenececeeneceseeees 26
The secret-Lite OF Caterpillars... s.ccccecdtcagursdessiy vteastrurcasdesecentateocardees Pg
PL IGACLUTD S aitaMastraieh eas inetastoniauh cod teatetterscentcrsloaiuuernsenl esd Lensuetiatgrhceiiegioaesneateosiyyiawhiwbacoer nei 28
Under the Microscope - Leaf-infesting nematodes .............ceccccesscccceseeccceneceeeeeeceeeeees 28
Merging photos to improve depth of field... eeeeeeeees 29
NOU ASK SON sss Gohan pdestisants Uubeaielecvyeatu dG eysagulshtnsde ds caddeemedaaardetearasadcebnadelenassababendadeannts 29
ECDC Er FOS PAINTS. walnts stiveces snavaratetiwesensnteaerstsueksenaeaapertediwece nepaeabaietaweseaseaantred eensensnanrey 3]
Magazine of the Butterfly and Other Invertebrates Club 454 Z Page 3
CREATURE FEATURE
An Introduction to Paropsine Leaf Beetles : John T. Moss and
Richard Zietek
Identification and brief description
These beetles belong to the family Chrysomelidae, subfamily Chrysomelinae, the
largest subfamily in Australia, which includes some 750 species in 42 genera. They
are in the tribe Paropsini, of which the commonly observed genera are Dicranosterna,
Paropsis, Paropsisterna and Trachymela |the related genus Chrysophtharta Weise
having recently been incorporated into Paropsisterna (Reid, 2006)]. Identification of
adult paropsine leaf beetles to species level 1s difficult due to the lack of useful keys.
Chris Reid (pers. comm.) defines paropsine beetles as “chrysomelines with elytra
extended at the sides to hide the body in lateral view and which feed on eucalypts and
wattles”’.
Adult paropsines range in size generally from 4 mm to 18 mm and many species have
quite colourful markings (which often fade after death) with patterned thorax and
elytra. Adult beetles look rather like ladybird beetles, Coccinellidae, but the structure
of the tarsi (feet) and antennae are different. Leaf beetle antennae are up to half as
long as the body, filiform (slender) and usually uniformly multi-segmented. Ladybird
beetle antennae are much shorter, have thickened (‘clavate’) tips and can be held
tightly against the head and thorax. There are several more technical characters that
better separate these two lookalike families which readers can access from other
sources. Due to the high diversity of species and poor current knowledge of the
taxonomy of the group, distributions of individual species are generally not recorded.
Some common examples
Some paropsine leaf beetles are major pests of eucalypt plantations and can cause
serious defoliations eg Paropsis atomaria, Paropsisterna cloelia and P. bimaculata,
this last “‘a notorious forest pest in
Tasmania” (Lawrence and Britton,
1991). The eucalypt feeding
Paropsisterna sexpustulata complex
involves at least 6 species which are
difficult to separate. At least two of
these, P. sexpustulata (Marsham)
and P. beata (Newman), are 10 to
14 mm long, ovate and convex (or
dome-shaped), shiny black species,
with six orange spots on the elytra
(wing covers) and two on the Paropsisterna cloelia
thorax. The former species appears Photo Russel Denton (RD)
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 4
to have at least two colour forms: the typical orange-spotted form and a yellow-
spotted morph. Honan (2008) illustrates this latter colour form as Paropsis sexguttata
and the Queensland Museum’s ‘Wildlife of Tropical North Queensland’ illustrates the
typical form as ‘Paropsis sexguttata complex’.
Paropsisterna sexpustulata (12mm long)
Orange-spotted form Yellow-spotted morph
Photos Peter Hendry (PH)
Dicranosterna, formerly placed 1n a separate tribe (Dicranosternin1), contains several
common Australian species. D. picea is a common wattle feeding species in
southeast Queensland and northern New South Wales. It is often found on “Black
Wattles” — Acacia concurrens, A. leiocalyx etc. At 14 mm long, it 1s one of our larger
species. Hockings (1980) illustrated larva, pupa and adult as Paropsis brunnea. Peter
Chew’s 2004 CD-ROM ‘Brisbane Insects and Spiders’ illustrated it as Paropsis
immaculata. However, Chris Reid reports that the author’s more recent website
correctly identifies the two common brown species, D. picea and D. immaculata. D.
circe, at 11 mm, 1s also a wattle feeder. It has a common white form and a less
common yellow morph. Hawkeswood (1987) illustrated it as Paropsis pedestris
Blackburn. In southeast Queensland it feeds commonly on Hickory Wattle (Acacia
disparimma — was A. aulococarpa).
oe , 4 1
Dicranosterna picea - 14 mm long adult and larva (RD)
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 5
a / i*
- he - a e* es %~. ®. .
&. , el 7s
Ge ae oeete%a
Figs. 1, 2 & 3 - Dicranosterna circe (adults 10 mm long) Fig.4-Larva Figs. 5 & 6—Pupae
Photos - Figs. 1,4,5&6 (PH) Figs. 2&3 (RD)
Lifecycle
Eggs are laid directly onto leaves or stems near new growth, usually in patterns
characteristic of individual species, either singly, or end to end in a line, or side by
side in rows or in a collar around a leaf stem. Eggs are vulnerable to predators such as
ladybirds, predatory bugs and tiny parasitic wasps. Newly hatched larvae feed
eregariously (in a group), at first, chewing patches on the leaf surface. As they mature
they may stay together or feed by themselves. Fully developed larvae move down the
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 6
tree to pupate in the soil or leaf litter. According to Gunter Maywald (pers. comm. ),
P. sexpustulata feeds on eucalypt foliage and over-winters as adults under loose bark
at the base of the host trees. Moore (1996) reported this (and the sibling species P.
beata) as feeding “in summer on various species of feathery-leaved wattles, and out
of season, are often to be found hibernating under loose bark of standing gum trees”’.
Lois Hughes (pers. comm.) has captive individuals that are currently feeding on the
eucalypt leaves that they were found on! It 1s our opinion, and that also of Dobrosak
(2001), that paropsine species can be found on trees and shrubs of other species
adjacent to their actual host plants. This would explain the apparent anomaly of
Moore, 1996. Reid (2006) reviewed host records, but not all species hosts were
identified.
Many of these beetles are relatively long-lived and take readily to captivity. They can
make charming and colourful little pets! Some Paropsis larvae defend themselves by
producing hydrocyanic acid from glands in the abdominal segment 8. Many adult
beetles also produce this chemical, so care should be exercised when handling these
insects.
References
Dobrosak, D. 2001. Notes on the biology and distribution of Paropsisterna
semifumata (Blackburn) (Coleoptera : Chrysomelidae) in southeastern
Australia. Australian Entomologist 28 (4) pp105-110
Hawkeswood, T. 1987. Beetles of Australia. Angus and Robertson Publishers
Hockings, F.D. 1980. Friends and Foes of Australian Gardens. A.H. & A.W.
Reed Publishers
Honan, P. 2008. Beetles and Bugs — A Wild Australia Guide. Steve Parish
Publishing
Lawrence, J.F. and Britton, E.B. 1991. Coleoptera: in The Insects of Australia
(CSIRO) Vol 2, Second Edition. Melbourne University Press
Moore, B.P. 1996. A guide to the Beetles of South-eastern Australia. Fascicle
12, p194. Australian Entomological Press
Reid, C.A.M. 2006. A taxonomic revision of the Australian Chrysomelinae,
with a key to the genera (Coleoptera : Chrysomelidae). Zootaxa 1292: 1-120
Further Information
Chris Reid, Australian Museum & ABRS websites —
www.faunanet.gov.au/faunakeys/chrysomelinae intro.htm
www.environment.gov.au/biodiversity/abrs/online-
resources/fauna/afd/taxa/Chrysomelinae
DPI& F notes - Leaf Beetles (Paropsines) —
http://www2.dp1.qld.gov.au/hardwoodsqld/93 13 .html
Brisbane Insects - Leaf Beetles / Paropsisterna -
http://www.brisbaneinsects.com/brisbane_leafbeetles/EucalyptusLeaf4.htm
Magazine of the Butterfly and Other Invertebrates Club 454 a Page 7
Photographs — Russel Denton and Peter Hendry
Acknowledgements
Dr.Chris Reid - Australian Museum, Sydney, for reviewing the mss.
Gunter Maywald - CSIRO Long Pocket Laboratories, Brisbane, for helpful comments
Gallery of leaf-eating beetles, family Chrysomelidae, from Brisbane area
[photographs by Russel Denton (RD)| and Bolivia Hill NSW [photographs by
Peter Hendry (PH)]
Yur Yas
7 Re, .
Celtis Leaf Beetle — Menippus cynicus (RD) — Chrysomelid sp. (approx. 12 mm long ) (PH)
Paropsisterna sp. (approx. 7mm long) (PH) Paropsis maculata (10 mm long) (RD)
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 8
Paropsis obsoleta (RD)
Paropsisterna 8-maculata (7mm long) (RD) Paropsisterna sp (16mm long) (PH)
Paropsisterna nobilitata complex (approx. 7mm long) (PH) Paropsisterna sp. (RD)
VIPPL TPT PS PTET PART PFT PPO Pa PT Pe PT hd be
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 9
ITEMS OF INTEREST
An Interesting Record of the Hawkmoth Macroglossum prometheus
lineatum Lucas (Lepidoptera : Sphingidae) from the Northern
Territory : David Lane
Australia contains a rich fauna of hawkmoths (family Sphingidae) with around 70
species currently recognised. Within Australia the genus Macroglossum Scopoli was
the subject of a revision by Max Moulds in 1985, and currently contains 13
Australian species. The world fauna of moths belonging to this genus has a wide
distribution ranging from Africa and Europe through Asia, and extending to the Indo-
Australian region. It 1s especially rich in species in New Guinea and Indonesia.
Macroglossum species are often referred to as Hummingbird Hawkmoths, due to their
ability to hover in front of flowers for extended periods whilst they actively feed from
| the available nectar source,
| | | utilising their well developed
= \@ { — proboscis, or tongue. They
a \ i have a well developed “fan
iA’ \ tail” of expansible hair-like
brushes on the lower
abdominal segments, which
amongst other purposes serve
as a braking and control agent
in flight. This behaviour has
led to their popular observed
identity as being allied to
miniature Hummingbirds.
Various species may be active
during the day or at night —
most however are nocturnal, with a preference to begin feeding from flowers around
dusk. Some are noted migrants, with one particular species, Macroglossum micaceum
micaceum Walker, having been observed 1n conspicuous numbers in northern
Queensland and arriving in south east Queensland and northern NSW in following
weeks. Another species, Macroglossum vacillans Walker, can be quite prolific in
numbers during certain wet summers in northern Australia, particularly in close
proximity to its larval foodplant Strychnos (Loganiaceae) species. It appears to
migrate from northern areas in a southerly direction over a period of several nights,
with considerable numbers of adult moths turning up at mercury vapour light traps in
areas where no suitable foodplants grow.
V.
Fig. | Adult M. prometheus lineatum
During a visit to Darwin in March 2009, many Macroglossum larvae were found
feeding on a small tree Morinda citrifolia L. (Rubiaceae) at several areas, including
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 10
East Point and Leanyer. These larvae were reared through to adult moths which
proved to be M. prometheus lineatum Lucas. Final instar larvae leave the foodplant
trees to pupate and web together several dead leaves on the ground at a convenient
sheltered location, in which they pupate. Larvae of M. prometheus lineatum have also
been found feeding on M. citrifolia at Silver Plains, near Coen, North Queensland.
Adult moths of M. p. lineatum have been collected from Cape York to Mackay in
Queensland, as well as New Guinea and adjacent islands. The nominal subspecies
ranges from Sri Lanka and India, through Malaysia, Indonesia and the Philippine
Islands (Moulds 1985).
M. prometheus lineatum has previously been recorded from the Northern Territory at
Rimbya Island, Cape Wessel (Moulds 1985). These records from Darwin confirm the
species distribution further to the west along the top coastal area of the Northern
Territory. The attached figures show the adult moth (Fig 1) and all larval instars (first
to fifth instar, Figs 2-6) as well as the pupa (Fig 7).
—_as
Fig.2- 1“ instar Fig.3- 2™ instar Fig.4-3"™ instar Fig.5—4" instar Fig.6—5™ instar Fig. 7 —Pupa
Photos David Lane
PIPT PTET PAPI TPT Pg PIP Pa PT bd PF Pe Pa PT bd bg
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 11
Reference
Moulds, M.S., 1985. A review of the Australian hawk moths of the genus
Macroglossum Scopoli (Lepidoptera : Sphingidae). Australian Entomological
Magazine 12(5): 81- 105
KREEKKEKKEKKKEKRKEKEEEE
Jewel Beetles (Coleoptera: Buprestidae): some views and notes
: Murdoch De Baar debaar@powerup.com.au
Jewel beetles are some of our most colourful insects, often displaying stunning
metallic blues and greens, with red and yellow splashes, whilst flashing around in the
bright sun. Further to the 1000-odd named species, there are also many undescribed
species in Australia.
‘Jewels’ or ‘rough diamonds’? Most of
these beetles are stem or trunk borers (where
the general biology is known), however little
is known about the majority of them, other
than their original anatomical descriptions.
We do know about our Hoop Pine jewel
beetle, Prospheres aurantiopictus which has
larvae that sustain slowed development of up
to 25 years in seasoned timber, because it
pops out under your nose, from your prized
pine table that you paid good money for!
However adults are not able to re-infest
seasoned timber, so exit holes should be
packed with wood filler and painted over.
——E—-—
Fig. 1. Hoop Pine jewel beetle chewing
foliage of a Hoop Pine (Photo M. Ramsden )
—
Fig. 2. Hoop Pine jewel beetle pictured shows a Fig. 3. Hoop Pine jewel beetle pictured shows
yellow-spotted form (Photo M. Ramsden ) a red-spotted form (Photo M. Ramsden )
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 12
Michael Ramsden, a Plantation Health Officer of the Forestry Plantations
Queensland, has photographed the three adult colour forms of the Hoop Pine jewel
beetle (Figs. 1, 2, 3). He has observed adults chewing Hoop Pine foliage at Imbil
State Forest in southern Queensland.
Pseudotaenia waterhousei (Fig. 4) is a large 30 to 50 mm long bronze green species
with powder yellow overlay, which bores into the trunks of wattle trees Acacia
leiocalyx at Dunmore State Forest via Cecil Plains, south Queensland. The larvae
which can be 75 mm long, cause trees to snap 1n the middle, giving an appearance of
storm damage, particularly considering that activity 1s often present on elevations or
ridges. The species has also been noted at Barakula State Forest via Chinchilla,
Queensland and according to literature, the species 1s known from central western areas
of southern New South Wales to southern Queensland. Adults, when disturbed, often
fly from trunk to trunk and create a loud buzzing as it flies out from behind you. The
species shows a preference to wattle thickets. A larva sinsiaiiainas 90 mm long, collected
by Forest Pathologist Geoff
Pegg, from a Brigalow stem
Acacia harpophylla, near
Tambo, south western
Queensland, was probably
Pseudotaenta ajax, a very
similar beetle in appearance
measuring about 60 mm as
an adult. E. Adams in the
News Bulletin of the
Australian Entomological
Society, Nov. 1966,
discusses how he used a rifle
to bring down his first | | |
, ; Fig. 4. The jewel beetle Pseudotaenia waterhousei near its
specimens of P. ajax from the i a, Spi
emergence exit hole on an Acacia leiocalyx trunk at Dunmore
side of Brigalow trunks at State Forest, south Queensland, 31 Dec. 1985.
Edungalba near Duaringa, (Photo Murdoch De Baar)
Queensland. He later
observed oviposition having occurred on damaged trunks. Mabel Hobler (as
Mrs.F.H.Hobler) who also lived in the Duaringa area, wrote in the Queensland
Naturalist (1925) that she observed oviposition, larval tunnelling and adults emerging
from the trunks of Brigalow.
At 40 to 50 mm, Stigmodera fortnumi (Figs. 5, 6) 1s a spectacular beetle adorned in
combinations of green and yellow. Normally unseen in set museum specimens, are
brilliant green flashes from the upper abdomen when the beetle is in flight (Fig. 5). A
loud buzzing overhead, heralds an incoming adult about to land on some paperbark
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 13 |
tea-tree (Melaleuca) or eucalypt flowers during the December/ January period at
Dunmore State Forest, via Cecil Plains, south Queensland. These beetles often land
too high in tree canopies to be closely examined. This jewel beetle is known from
South Australia to southern Queensland, however, within this “wide distribution’, its
actual presence 1s probably only in a narrow disjointed band and little else is known
about this chunky, showy jewel. It is a shame that museum specimens’ colours dull
somewhat, so the only way to fully appreciate their brilliant lustre 1s from
photographs or under natural conditions of around 40 degrees C. and lots of flies!
L
Fig. 5. Upper surface and upper adbominal views Fig. 6. Underside view of the large jewel beetle
of the large jewel beetle Stigmodera fortnumi from Stigmodera fortnumi from Dunmore State Forest,
Dunmore State Forest, southern Queensland, 4 Jan. southern Queensland, 4 Jan. 1986, highlighting its
1986, highlighting its magnificent colours. magnificent colours of metallic green, yellow and
(Photo Murdoch De Baar) deep blue. (Photo Murdoch De Baar)
Curis viridicyanea (Fig. 7) 1s only
15 to 20mm long, but makes up for
its size with stunning metallic
ereenish gold. Some specimens are
an equally brilliant blue. These
beetles can also be seen at Dunmore
S.F., via Cecil Plains, south
Queensland, on Melaleuca foliage
or flowers. However, little is known
about them and they are not often
seen. The recorded distribution of
this species is from northern New
South Wales to southern Queensland,
, ; se Fig. 7. A bluish-green colour form of Curis
probably mainly in the Callitris, viridicyanea on Paperbark Tea tree flowers.
Melaleuca environments. (Photo Murdoch De Baar)
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 14
Diadoxus erythrurus, the Cypress Pine jewel beetle (Fig. 8) oviposit into stressed
and/or burnt or damaged cypress pine ( Callitris spp.) trees, or logs that are freshly
cut and not hauled to the mill for processing quickly enough. This is referred to as a
log hygiene problem. The larvae tunnel under the bark and into the cambial layer
where they feed, occasionally penetrating a little further. The larval development is
slowed in seasoned timber, but emergences after 2 years are rare. As for the Hoop
Pine jewel beetle, the exit holes can be plugged with wood filler and painted over, as
the adults are unable to re-infest
the seasoned timber. Also, as for
the Hoop Pine jewel beetle, we
would know little about this
beetle if it did not pop out under
your nose, from your prized
polished cypress timber
supposed to be “borer resistant’.
The “true-wood” of cypress 1s
reasonably borer resistant, but
sometimes pupation chambers
Fig. 8. Cypress Pine jewel beetles Diadoxus are also cut into this wood.
erythrurus on a cut trunk of a Cypress tree Callitris Ame:
glaucophylla. (Photo Murdoch De Baar) The Cypress Pine jewel beetle has
a wide distribution from southern
West Australia across to Queensland and includes the Moreton Bay islands in
southeast Queensland, where I have observed it flying around Callitris columellaris
foliage.
Occasionally in Brisbane,
Stigmodera goryi (Fig. 9) cuts a
“mean exit hole” in a stressed
Grey Gum (Eucalyptus
propinqua) trunk. This 35 mm or
so jewel beetle is not as brilliant
as some of its relations but is still
attractively adorned with yellow
wing covers (elytra). Within
Brisbane, specimens have been
recorded at Bardon, Long Pocket
and Bowen Hills, although it’s
distribution 1s mainly coastal
New South Wales and
Queensland. Adults are attracted
to flowers of Leptospermum.
Fig. 9 Stigmodera goryi from Long Pocket in Brisbane
20 Dec. 1986 (Photo Murdoch De Baar)
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 15
Jewel beetles have been very popular with amateur entomologists, so it 1s very
surprising that so many biologies are poorly known. The emergences of some species
are initiated by wild storms or extended wet weather, which can make observations
uncomfortable and driving home through muddy roads hazardous, particularly if that
road becomes a tributary of the local creek! Obviously the tunnellings of most jewel
beetle larvae rarely catch our attention, otherwise entomologists’ extension loads
would blow out of all proportion. The reason for this 1s that activity often occurs in
natural environments, sometimes in remote areas, in noncommercial tree trunks, or at
low levels in commercial tree species. Some emergences are from old dying trees
ignored as a timber source and a number of jewel beetles are known to bore down
into the roots of trees. It is difficult for the amateur entomologist to cut and carry
home billets from those dying trees that may have jewel beetle activity. It is also
known that some jewel beetles can be observed in numbers one season and then not
be seen for years, save perhaps a couple of specimens. The explanation for this 1s
poorly understood, but perhaps it’s to do with long-lived larvae and synchronised
larval development. In some countries jewel beetles are used as jewellery.
Some adult jewel beetles are very difficult to observe, as they prefer to remain on the
topmost flowers of tall trees and some specialists have climbed trees, with some
success, to try to overcome this problem. Just consider: smooth-barked Angophora
(Myrtaceae) vigorously attract jewel beetles to their flowers, are extremely slippery in
rain and are notorious branch droppers. Do you still want to find out what’s on the
topmost flowers?!#
I i i i i ie i Ee i i sie
Life History Notes on the Narrow-brand Grass-dart, Ocybadistes
flavovittata flavovittata (Latreille, |1824|) and the Greenish Grass-
dart, Ocybadistes walkeri sothis (Waterhouse 1933) Lepidoptera:
Hesperiidae : Wesley Jenkinson
The two most frequently encountered species of Ocybadistes butterflies within South
East Queensland suburban gardens are Ocybadistes flavovittata flavovittata (Narrow-
brand Grass-dart), and Ocybadistes walkeri sothis (Greenish Grass-dart), with the
latter species being more geographically widespread and generally more numerous.
(Not be confused with the adults of two other similar looking species from the
Taractrocera and Suniana genera also breeding in my garden!)
Many butterfly enthusiasts overlook the smaller hesperids. This is often because of
their generally small size, presumed lack of vibrant colour and the degree of difficulty
to correctly identify the adults. However, they are interesting small critters to have
darting around the garden.
Magazine of the Butterfly and Other Invertebrates Club 454 7 Page 16
Ocybadistes flavovittata flavovittata (Narrow-brand Grass-dart)
~
F Mu
Ocybadistes walkeri sothis (Greenish Grass-dart)
In my garden, at Beaudesert, I have observed several females of the two species
ovipositing their eggs singly, with their preference for the underside of a leaf. Fisher,
1978, documented that females of O. w. sothis oviposit eggs singly on the upperside
of leaves.
On narrow leaf grasses the females often settle on the leaf top and curl the abdomen
below the leaf to oviposit. I have watched a female O. w. sothis ovipositing on a wide
leaf grass, the exotic Green Panic Megathyrus maximus (formerly Panicum
maximum). She settled on the upper surface of the leaf and then crawled below the
leaf. She then positioned herself parallel along the leaf and laid an egg tightly next to
the midrib.
Having raised several adults of the two species from eggs, at different times of the
year, I have observed the habits of the immature stages are very similar, but they do
show slight differences in their physical appearance.
The eggs of both species were similar in size and shape, being dome shaped, smooth
(with a very fine pattern) and with an approximate size of 0.5 mm high x 0.8 mm
wide.
Egg of Ocybadistes flavovittata flavovittata
Several eggs were collected from a female O. f. flavovittata. They
were pale green in colour when laid and remained this colour
throughout their duration, unlike the colour change seen 1n maturing
eggs of O. w. sothis.
Egg of Ocybadistes walkeri sothis
Several eggs were also collected from a female O. w. sothis, which
were creamy-white when laid. After two days the colour had
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 17
eradually changed to cream and the eggs had developed a broken, pinkish-red lateral
band and an apical spot.
Several larvae of the two species were raised in captivity and they had very similar
habits. Newly emerged larvae consumed most of the eggshell after emergence and
later formed a small cylindrical shelter, approximately 3-4mm in length, towards the
leaf apex of the host plant. To do this they chewed small transverse cuts from the
outer edge of the leaf towards the midrib and then curled the outer edge of the leaf
inwards by tensioning silk threads forming the cylindrical shelter. Feeding larvae
consumed both sides of the leaf margin distal to the shelter, stopping at the leaf
midrib. This caused the cylindrical shelter to hang and the larvae ate from the lower
part of the shelter. As the larvae grew and consumed most of the leaf and shelter, they
constructed a new shelter to accommodate their larger size. When raised on thin leaf
erasses the larger larvae stitched several leaves together with silk to form the shelter.
The larvae remained inside the silk-lined shelter during the day and emerged chiefly
at dawn and dusk to feed. (Fisher, 1978, described similar larval behaviour for O. w.
sothis)
Larvae raised indoors occasionally constructed their shelters and fed briefly during
daylight hours.
Larvae of both species completed five instars and attained a length of approximately
25mm.
' _ \
¢ 4 ps!
a : ’
1* & 5" instar larvae of Ocybadistes flavovittata flavovittata
1 & 5" instar larvae of
Ocybadistes walkeri
sothis
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 18
In captivity the pupae of O. w.
sothis were found inside the final
larval shelter. (As noted by
Fisher, 1978.) The posterior end
of the final instar shelter was
stitched closed and the anterior
end was left slightly open for the
adult to emerge. The three pupae
of O. w. sothis raised in captivity
had a fine, white, waxy powder
coating on their surface. This
powder was absent from all of
the O. f. flavovittata pupae
raised. Pupae of both species
Pupa of Ocybadistes flavovittata flavovittata measured 15 mm in length
ae
When raised in captivity O .f. flavovittata eggs hatched in 10 days, larval duration
was 54 days and pupal duration 27 days - the life cycle being completed in 91 days.
(From 27" April 2008 to 27" July 2008.)
Likewise O. w. sothis eggs hatched 1n 12 days, larval duration was 66 days and pupal
duration 10 days - the life cycle being completed in 88 days. (From 9" September
2006 to 26"" November 2006.)
At Beaudesert, I have adult records for both species during eleven months of the year,
with possibly three or four overlapping generations per year. Adults are fewer in
number during the cold winter months and absent in July.
I have discovered that, locally, a commonly used host plant of O. f flavovittata 1s the
native grass Green Couch (Cynodon dactylon). Undoubtedly, other species of soft
erasses are utilised as larval host plants, including species known to be used by O. w.
sothis as listed in Braby, 2000, and Moss, 2005.
The wingspan of adults of both species show slight size variation but average
approximately 20mm for both sexes. The size and shape of the orange wing markings
also show slight variation for both sexes of the two species. The correct identification
of the adults can cause some grief, however examination of the forewing sex-scales
should identify the males. The females can be quite difficult to place and examination
of the genitalia is the best guide. The male sex brands are illustrated in three historical
books by Common and Waterhouse and two more recent books by M.F. Braby.
The flight pattern and habits of the adults of both species are very similar. Typically
both sexes settle on the upperside of grass leaves to bask 1n sunny conditions. The
males of both species typically defend small territories, perching on grass leaves and
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 19
engage in very rapid chases. The adults are readily attracted to the flowers of a wide
range of native and exotic plant species.
Typical basking stance of a male Ocybadistes Mating pair of Ocybadistes walkeri sothis
walkeri sothis
Photos Wesley Jenkinson
References:
Braby, M.F., 2000. Butterflies of Australia — Their Identification, Biology and
Distribution. vol 1. CSIRO Publishing
Fisher R.H. 1972. Butterflies of South Australia. Government Printer, Adelaide S.A.
Moss J.T. 2005 Butterfly Host Plants of south-east Queensland and northern New
South Wales. 2™ rev. edition, BOIC
i ee
The Flame Flatwing (Austroargiolestes amabilis) : Ross Kendall
The Flame Flatwing is a beautiful
damselfly usually 42-45mm long, found
near streams in dense montane rainforest
in southern Queensland and coastal New
South Wales.
I have observed males 1n an open sunny
patch 100 metres from a creek on the
upper section of Branch Creek track,
Bellthorpe Forest, in summer. This spot in
the Conondale Range 1s at an altitude of
370m at 26°52’34” S, 152°42’6” E.
Mid morning on 10" March 2007, with the
actively ovipositing on Broken Bridge
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 20
Creek at the eastern end of Bellthorpe Forest. This 1s at an altitude of 470m at
26°49°30"S, 152°44°12”E. The area has good coverage of rainforest and the creek
was running freely.
One female was seen ovipositing in moss close to the
water and the one pictured was busy laying eggs in
crevices on a log about half a metre above the water.
I have included a close up of the tip of her abdomen
showing the ovipositor. It would be an interesting |
challenge to collect some eggs, hatch them and raise o “=e
the nymphs through to adulthood as the juvenile stages
of this species are unrecorded.
Photos Ross Kendall
Tip of female abdomen
References:
Giinther Theischinger and John Hawking, 2006. The Complete Field Guide to
Dragonflies of Australia. CSIRO Publishing, Collingwood Vic.
Natrass, Ric, 2006. Dragonflies of South East Queensland — A Field Guide. Rick
Natrass
2K 2K ok ok ok ok ok ok ok ok ok ok ok ok ok ok ok ok of
4" Biannual Moth Meeting-Canberra 2009: Peter Hendry
I had the pleasure of being invited to
the 4"" biannual moth meeting, held at
the CSIRO’s Division of Entomology
in Canberra, over the weekend of the
1-2" August 2009. I would have
paid good money just to be a fly on
the wall, but to be able to participate
was a wonderful experience!
The meeting was an informal affair,
with a few short talks on the Saturday
afternoon. Some of the subjects
covered included Max Day’s work on
the Scribbly Gum Moth, showing the Delegates to ANIC moth meeting
possibility of there being some twenty
plus species involved. John Hawking spoke of his work to date revising the
Crambidae subfamily Acentropinae. These are the moths that have aquatic larvae.
Michael Braby took us on a tour of the Northern Territory museum in Darwin.
Donald Hobern and Nick dos Remedios from “Atlas of Living Australia” spoke of the
web portal they are setting up to hold metadata on all Australian animal species and
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 21
Don Sands talked about his concerns of controlled burning on the environment. This
was further dealt with in a presentation and discussion on the Sunday morning.
On a personal note I was delighted to be able put names on some of the moths in my
collection with assistance from Ted Edwards, John Hawking and Bart Hacobian and
being able to search through the Australian National Insect Collection. It was
wonderful just to pick up on the discussions being held amongst delegates and Len
Willan’s helpful tips on photography. The highlight for me was a one on one
demonstration on dissection of moth genitalia by Marianne Horak. This has eased my
fears a bit and I certainly intend to set myself up and give it a go.
Marilyn Hewish, in the absence of Peter Marriott, launched the second volume of
Moths of Victoria (see review 1n this issue). Marianne announced that the boys from
“Atlas of Living Australia” had taken over the web hosting of “Australian Moths on
Line’. It can now be found at: http://www1l.ala.org.au/gallery2/ The site now
includes all of the named Tortricidae, including their relative sizes.
Until 2011, happy mothing.
i ee ee
Cuckoo Wasps (Hymenoptera : Chrysididae) : Peter Hendry
In our last magazine (Issue No. 53
June 2009), Densey Clyne wrote of
her observations of the Mason
Wasp. In the article she mentions a
parasitoid wasp in the genus
Stilbum had been seen near the
Mason Wasp nest.
I had the opportunity to photograph
one of these wasps while it crawled
up and down the brickwork of my
house. It was obviously looking for
mud wasp nests, which are often
created against the mortar between
the bricks.
Cuckoo Wasp (Photo Peter Hendry)
These Cuckoo Wasps belong to the family Chrysididae that contains four subfamilies,
Amiseginae, Chrysidinae, Cleptinae and Loboscelidiinae. Of these Cleptinae only
occurs in the Northern Hemisphere. The Amiseginae and Loboscelidiinae parasitise
the eggs of Phasmids (Stick Insects). The Chrysidinae parasitise wasps in the families
Sphecidae and Vespidae.
The photo above is of a member of the subfamily Chrysidinae. They can be either
metallic green, blue, violet or red. They have the ability to roll into a ball if attacked
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 22 |
by the nest-building wasp. The larvae either eat the other wasp’s larvae or eat the
food provided by the other wasp for its larvae.
AT THE LIGHT TRAP
The Return of the Crambidae : Peter Hendry
I spent the Easter weekend of 2008 on my bush block west of Bundaberg and
reported in the June 2008 issue this magazine on “The Night of the Crambidae’”’. This
was when, in one night, I had 15 different species of Crambidae moths come to light.
This last Easter (2009), on my return to the same site with a bit more equipment, I
was able to run two light traps about one and a half kilometers apart. Unlike last year,
no one night proved better than the next, but I was able to pull in 24 different species
of Crambidae over three nights.
Of these 24 species I have been able
to put names to 22. Four of these
belong to the subfamily Acentropinae;
the remaining 19 belong to the
subfamily Pyraustinae. While at the
recent moth meeting in Canberra I met
with John Hawking who 1s revising
the Acentropinae. He was particularly
interested in my specimen of Elophila
aristodora (Turner, 1908) {wingspan
c 1lmm}. The only other material of
this species he has available for his
Parapoynx polydectalis Parapoynx villidalis
research is over 30 years old and he is having trouble extracting a complete DNA
sequence. Arrangements are being made for me to send him material from my
specimen. The Acentropinae are known for their aquatic larvae. John tells
the story that while on a field trip with Mike Halsey, they witnessed a female
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 23
Acentropinae moth dive into the water, swim under a rock and after some time re-
emerge. On turning over the rock they found a freshly laid clutch of eggs!
The other 3 Acentropinae all belong to the genus Parapoynx. These were P.
polydectalis (Walker, 1859) {wingspan c 14-20mm}, P. stagnalis (Zeller, 1852),
which also made an appearance at Easter 2008 and P. villidalis (Walker, 1859)
{wingspan c 17mm}. Apart from knowing these moths have aquatic larvae, I could
find nothing else on their biology. I am eagerly awaiting the completion of John’s
work.
Glyphodes canthusalis Archernis callixantha
Some of the more spectacular
Pyraustinae to appear included
Archernis callixantha Meyrick, 1886
{wingspan c 20-23mm}. I have also
encountered this species west of
Babinda 1n north Qld on the 23/10/2008
and at home at Sheldon, Redland City
east of Brisbane on the 20/04/2007. It
occurs from Cape York to northern
NSW and Indonesia (Common 1990). Nausinoe pueritia
Glyphodes canthusalis Walker, 1859
{wingspan c 25mm} was a first time encounter. It also has a distribution from Cape
York to northern NSW (Common 1990). It is listed on the web page
http://hk.geocities.com/pyralidaetw/pyra.30.htm as also occurring in China, India,
Nepal, Borneo and Indonesia. Nausinoe pueritia (Cramer, |1780]) {wingspan c 25-
30mm} with its long abdomen, made its second appearance on the block. The first
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 24
Tatobotys biannulalis Pycanarmon meritalis
was on the 8/11/2007 and I have also collected it seventy-odd kilometers NW of
Mackay. Its distribution covers the Northern Territory, Cape York to northern NSW
as well as India, Sri Lanka and Indonesia (Common 1990). With an equally
impressive abdomen, though far less ornate, 1s Tatobotys biannulalis (Walker,
[1866]) {wingspan c 17mm}. In Fiji the larvae have been found scavenging in debris
at the base of rice stools and it 1s suspected they feed in similar situations in various
grasses. Pupation takes place within a frass-covered cocoon at the stem base
(Hinckley 1964). Pycnarmon meritalis (Walker, 1859) {wingspan c 14mm} was
another first time visitor.
The remaining specimens of Pyraustinae to come to light this Easter (but not figured
herein) were Eurrhyparodes bracteolalis (Zeller, 1852), Eurrhyparodes tricoloralis
(Zeller, 1852), Herpetogramma licarsisalis (Walker, 1859), Maruca vitrata
(Fabricius, 1787), Metasia tiasalis (Walker, 1859), Metoeca foedalis (Guenée, 1854),
Nacoleia rhoeoalis (Walker, 1859), Notarcha aurolinealis (Walker, 1859), Omiodes
diemenalis (Guenée, 1854), Parotis sp. (Walker, 1859), Pyrausta testalis (Fabricius,
1794), Rehimena surusalis (Walker, 1859) and Spoladea recurvalis (Fabricius, 1775).
It was interesting to note that of these species, the most recently named 1s Elophila
aristodora (Turner, 1908) with the other namings dating back to Spoladea recurvalis
(Fabricius, 1775).
Photos Peter Hendry
References:
Common, I.F.B. 1990. Moths of Australia. Melbourne University Press
Hinckley, A. D. 1964, Ecological Notes on the Larvae of some Pyraloid Moths In
Fiji, Pacific Insects 6 (2) : 234-241
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 25
BOOK REVIEWS
Moths of Victoria Part 2: reviewed by Peter Hendry
e_* Ly Ff As Of Victor Ya |
The second in this series of booklets
attempting to illustrate all of the moths
that occur in Victoria has just been
released. It is by Peter Marriott and his
team at the Entomological Society of
Victoria and covers the superfamily
Noctuoidea.
Six of the seven Noctuoidea families
occurring in Victoria are covered. These
are Oenosandridae, Notodontidae,
Lymantriidae, Arctiidae, Herminiudae
and Nolidae. The booklet is well set out
with a colour tab on the top right corner,
being a different colour for each family.
A pinned specimen of each moth 1s
shown and a scale bar at the bottom of
the page gives the reader an idea of its
size. There are many photos of live
moths, pupae, larvae and eggs. With over
170 species illustrated and the fact that
many of these moths have a larger
distribution than Victoria, this booklet is a must for anyone interested in the moth
lepidoptera of Australia
fPETER MARRIOTT
As with Part 1, this booklet contains a CD, which in this case includes another 300
pages of images and information. The CD contains information on the biology and
distribution of each species, adding over 500 images. There are several other items on
the CD, being a glossary, a checklist of the included moths, a list of moth families
with a brief description, updates to part 1, a look into the future with a description of
what will be on parts 3 and 4 and a note on how to stay informed of the progress and
how to receive updates.
All in all it is a great effort. For those wishing to purchase a copy you can contact
Peter Marriott at vicmoth@entsocvic.org.au or write to lan Endersby, 56 Looker
Road, Montmorency, Vic. 3094
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 26
The Secret Life of Caterpillars by Densey
Clyne : reviewed by Lois Hughes
I can think of no more appropriate way to introduce
this delightful book, than by using Densey’s own
words.
“What exactly is a caterpillar’? Are caterpillars just
ereedy, guzzling grubs? Is there more to them than
being squashy sausages that birds love to eat, or that
humans love to spray with insecticide? The answer 1s
yes!”
I just love secrets, especially of the insect variety.
This book reveals many aspects of the secretive lives
of caterpillars as they journey to adulthood, the dangers they encounter and the
strategies they use to outsmart their predators.
Written for the young and young at heart, the book contains a wealth of knowledge
and displays the infinite patience and skill of the author and her obvious enjoyment
and fascination with her subjects. It captures the stunningly beautiful, the delightfully
humourous and the cunningly disguised — Creation at its ... well most gloriously
creative!
Every page of this large (28.5 x 22 cm) glossy, hard cover, 48 page book 1s
beautifully designed. The engaging narrative, complemented by the many superb
photos illustrating the text, introduces the young reader to technical terms. A two
page glossary expands on and more fully explains these terms. A list of scientific
names of the moths and butterflies pictured follows an activities page.
Densey Clyne’s work is already well known to many of us. Two of her previous
books “Cicada Sing-Song” and “How to Attract Butterflies to your Garden” are
publications we have enjoyed in the past, but this latest one 1s the best yet. Densey 1s
an internationally known author, photographer and wildlife documentary producer
and has received numerous awards. She 1s also a much valued member of BOIC and
her article on the Mason Wasp in the June ’09 issue of Metamorphosis Australia
illustrates her considerable writing skills, superb photos and patient and dogged
determination to uncover the secret lives of insects, all qualities which are apparent in
her latest book.
Densey’s own words are a fitting conclusion to this review. “Life after Life - What
does the butterfly sipping nectar in the sunshine remember of its days as a flightless,
leaf-munching caterpillar’? Does a moth negotiating its scented flight path through
the night recall its juvenile life earthbound among the leafy stems’?
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 27
We may never know the answers to those questions. What we do know of the
amazing double life of moths and butterflies is enough to surprise and delight those
with the eyes to see and the patience to watch.”
This is a book to enjoy and treasure.
Available from BOIC for $19.95 plus $8 P&H
ERRATUM
In reviewing material for an article on the “Mysterious Cycad Blue Butterfly” in
Metamorphosis Australia (No 53), I inadvertently overlooked an article by Dr. Don
Sands, titled “Host Changes 1n the Lycaenid butterfly Theclinesthes onycha onycha
(Hewitson): a possible preference shift?” published in Vol 35, issue 9, December
2007 News Bulletin of the Entomological Society of Queensland Inc. The original
observations therein are important and I apologise to Don for this omission.
There is an abstracted version of Don’s paper in the miscellaneous notes section, Vol
35 part 2, of the Australian Entomologist. John T. Moss
UNDER THE MICROSCOPE
Leaf-infesting Nematodes : Bob Miller
My neighbour is an avid orchid grower who puts on incredible displays in SROPPINE
centers all over Cairns. Hypolycaena -
danis turneri (The Orchid Flash) love
his collection of tasty orchids!
Unfortunately one of his orchids
looked like it was facing certain death.
Its leaves were rotting and falling off,
leaving a slimy mess in the pot, so he
brought it over to me to see if I could
help.
I immediately took the pot into my
study and placed the orchid under the
Butterfly and Other Invertebrates Club
microscope. After a bit of searching and
dismantling of the orchid, I noticed small
white worm-like critters, fairly abundant around the base of the dead leaves, so I took
a few photos of these for a positive identification.
Hypolycaena danis turneri
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 28
I informed the next door neighbour that it looked like he had an infestation of
nematodes and emailed the photos to him. He quickly sent these off to be identified.
The reply we received back from Tony Pattison, a nematologist from South
Johnstone, stated that they are indeed nematodes. They are a species of
Aphelenchoides, leaf-infesting nematodes, which are common in Australia on a wide
range of plants.
+ ' 3 .
P :
. < se .
: -
+
.
Nematode on orchid Close-up of nematode
Merging photos to improve “Depth of Field”
Upon taking multiple photos of butterfly eggs using the B.O.I.C. microscope camera
setup, we noticed that they all come out with a very bad depth of field, making them
unusable.
Example of trying to take a photo of a bunch of Varied Hairstreak (Jalmenus inous)
eggs:
Before After
Before: You notice that only a small proportion of the eggs are in focus.
After: With the help of a program called Helicon Focus we can merge a series of
badly focused pictures to create one crystal clear image of essentially anything you
wish.
DIPTPT PT PT PS PT PT PA PT PFT PI Pa Pe bd eT hd Pg
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 29
YOU ASKED
Hi Daphne,
I was wondering 1f you might know of
someone in the club who could help
identify the wonderful creature that one of
my friends had visit their house.
The beetle was found in the Tully area and
we would really love to know a bit more
about it. Please let me know if you need
more information.
Regards, Wendy Finlayson
Photo Alex Tessier
Hi Derrick, Wendy & Daphne,
The photo is of a Cerambycidae (longicorn beetle), Batocera frenchi and 1s a fig borer
as a larva. Normally you would need to be near a North Queensland rainforest to
obtain this beetle. The adults (often 50 mm or so) will come to the milky exudate
from the wound of a fig. Museum specimens often have the red spots on their elytra
faded a little. The SEQ equivalent is Batocera boisduvali. These beetles can “bite”
hard, as their tarsi (feet) are very capable of holding onto the target finger.
Best wishes, Murdoch De Baar
Se ae Se Se Ee
Question - The Mad Fan, correct name Grey Fantail (Rhipidura fuliginos), is often
seen in our garden. I was never able to see what it was eating until this morning I
could see small clouds of flying insects. I was able to capture two specimens with a
small net. The pictures I have sent are of this insect, one taken through the eye piece
of a microscope and the other straight macro. The insect 1s 4mm from the end of the
abdomen to the tip of those feathery feelers. Unfortunately I was unable to take any
pictures of the dorsum of the insect. It has
to me, a remarkable appearance. Like a
dragonfly, it has a long segmented
abdomen with terminal claspers. The |
single pair of wings is dragonfly-like, but a
the second pair are reduced to small clubs.
The feelers are moth-like. The eyes are
large. The flight of this insect is very rapid
and erratic and scaled up would equal the
speed of any aircraft! — Hilton Selvey
Answer - They are male chironomid midges (Chironomidae). Many species of
chironomid midges show "Iekking" behaviour where males form large groups and
wait for females to come and select them for mating. The behaviour also turns up 1n
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 30
other unrelated insects, such as many other flies, moths, ants, some heteropteran bugs,
many aquatic insects (mayflies especially). — Dave Britton
Further from Hilton - Thank you for finding out the name of the tiny insect that so
intrigues me. During the "Iekking" behaviour, the insect flies in straight lines for
about 10cm and then abruptly changes direction. To me it 1s astonishing that the Mad
Fan can get enough energy from these tiny insects to replace the energy used in
catching them plus their normal metabolic requirements.
BUTTERFLY AND OTHER INVERTEBRATES CLUB PROGRAMME
Walk in the Wallum with Swordgrass Browns
What: Walk in coastal heathland, through Swordgrass Brown Butterfly habitat, with possible
light trapping in the evening
When: Saturday, 10th October 2009, from 10 am
Where: Beerwah and Landsborough. Meet at the corner of Steve Erwin Way (old Glasshouse
Mountains Road) and Roys Road, Beerwah.
Bring: Water, hat, sunscreen, walking shoes, lunch and dinner if staying late
Contact: John Moss 3245 2997 Mobile (on the day) 0427 596753. It is essential to register if
planning to attend
Planning and Management Meeting
What: Our planning meetings are informative and interesting. As well as planning our
activities we share lots of information. All members are welcome as this activity is also a
general meeting of members.
When: Saturday, 14th November, 2009 from 1.30 pm
Where: Alisha’s Steward’s home (directions supplied on R.S.V.P.)
R.S.V.P.: Alisha on 3275 1186 or Daphne on 3396 6334
Mt Glorious Biological Centre/Mt Glorious Rainforest Walk
What: A visit to the Mt Glorious Biological Centre, followed by lunch and a rainforest walk.
Butterflies and stick insects are reared at the Biological Centre, and mounted insect specimens
from throughout the world are on display. The visit will be followed by lunch at the Maiala
picnic area, just past the Mt Glorious township. We can then take a walk through the
subtropical rainforest - the Maiala Circuit is a 2km walk which takes approx. | hour to
complete. There are additional walking tracks if people are interested in doing more.
PLEASE RSVP - we will contact the Biological Centre closer to the date to confirm numbers.
If the Biological Centre visit is cancelled, lunch and the walk will still take place.
When: 10:30am, Saturday 28th November 2009. Earlybirds are welcome to meet up for a
coffee beforehand in a nearby cafe. RSVP for details.
Where: We'll meet at 10:30am in the carpark of the Maiala picnic area, part of D'Aguilar
National Park, and head off to the Biological Centre. The picnic area is located on Mt Glorious
Road (the main road), just out of Mt Glorious township. It will be signposted. It takes approx.
70 mins to drive there from Brisbane City. We'll return to the picnic area for lunch and a walk.
Bring: Lunch, snacks, water, hat, walking shoes. PLEASE RSVP: By Monday 23rd
November 2009 to Alisha Steward a.steward@griffith.edu.au_ 3275 1186 (home),
0402 091 863 (On the morning of the excursion I will have the mobile phone turned on).
Magazine of the Butterfly and Other Invertebrates Club 454 7 Page 31
DISCLAIMER
The magazine seeks to be as scientifically accurate as possible but the views, opinions and
observations expressed are those of the authors. The magazine 1s a platform for people to
express their views and observations. These are not necessarily those of the BOIC. If
inaccuracies have inadvertently occurred and are brought to our attention we will seek to
correct them in future editions. The Editor reserves the right to refuse to print any matter
which is unsuitable, inappropriate or objectionable and to make nomenclature changes as
appropriate.
ACKNOWLEDGMENTS
Producing this magazine 1s done with the efforts of:
e Those members who have sent in letters and articles
e Lois Hughes who provides illustrations including the cover
e Daphne Bowden who works on layout, production and distribution
e John Moss, Murdoch De Baar, Dr Chris Reid and Dr David Britton for scientific
referencing and proof reading of various articles in this issue of the magazine
e Printing of this publication is proudly supported by |
Brisbane City Council
—_
fl
We would like to thank all these people for their TEL ha T
contribution. BRISBANE CITY
Dedicated to a better Brishane
ARE YOU A MEMBER
Please check your mailing label for the date your membership is due for renewal. If your
membership is due, please renew as soon as possible. Membership fees are $25.00 for
individuals, schools and organizations. If you wish to pay electronically, the following
information will assist you: BSB: 484-799, Account No: 001227191, Account name: BOIC,
Bank: Suncorp, Reference: your membership no. and surname e.g. 234 Roberts.
Butterfly and Other Invertebrates Club Inc.
PO Box 2113
RUNCORN Q. 4113
Next event — Walk in the Wallum with Swordgrass Browns, Saturday, 10th
October, 2009 (See Programme for details)
Magazine of the Butterfly and Other Invertebrates Club #54 — Page 32