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METAMORPHOSIS
MUSTRALIA
Magazine of the Butterfly & (ther Invertebrates ( lub
ISSUE No: 76 DATE: MARCH 2015 ISSN: 1839-9819
Price $6.00 http://www. boic.org.au
PLANNING AND ORGANIZING COMMITTEE 2014
President:
Vice President:
Treasurer:
Secretary:
Magazine:
Publicity and Library:
Excursion Convenor:
Committee Members:
Ross Kendall 07 3378 1187
John Moss 07 3245 2997
Rob MacSloy 07 3824 4348
Richard Zietek 07 3390 1950
Daphne Bowden (daphne.bowden] @bigpond.com) 07 3396 6334
Lois Hughes 07 3206 6229
Alisha Steward 07 3275 1186
Marie-Louise Johnson 0422 970 184
Jill Fechner 0417 793 659
PLANNING AND ORGANIZATION MEETINGS
A quarterly meeting is scheduled 1n 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 $30 for individuals, schools and organizations.
AIMS OF ORGANIZATION
To establish a network of people growing butterfly host plants;
e To hold information meetings about invertebrates;
To organize excursions around the theme of invertebrates e.g. butterflies,
native bees, ants, dragonflies, beetles, freshwater habitats, and others;
To promote the conservation of the invertebrate habitat;
To promote research into invertebrates;
®
e To promote the keeping of invertebrates as alternative pets;
@
@
To encourage the construction of invertebrate friendly habitats 1n urban areas.
MAGAZINE DEADLINES
If you want to submit an item for publication the following deadlines apply:
March issue — February Ist June issue — May Ist
September issue — August Ist December issue — November |st
Blue Tiger (Tirumala hamata hamata) — Painting by Elaine Allison - prints are
available direct from the artist; contact via email at elaineallisonart@gmail.com
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Magazine of the Butterfly and Other Invertebrates Club #76 — Page 2
FROM THE PRESIDENT
The proliferation of insects as a result of recent favourable weather conditions has
certainly attracted the attention of a large number of people and of the media. This
has provided an opportunity to inform a wider audience of the world of invertebrates.
As the Blue Tiger butterfly has been the main focus of public attention, this insect
features in our cover story and elsewhere. We thank Wesley Jenkinson and John Moss
who have combined to flesh out the knowledge of the readers of our magazine.
Elaine Allison’s painting is her first to be published here and I am sure you will
admire and appreciate the result of her artistic efforts.
Many thanks are owed to the various other contributors whose articles have made this
edition of the magazine an interesting and informative read. In particular, I thank
Kelvin Dunn who has taken the time to travel extensively, make meticulous
observations and produce detailed reports to share his discoveries with us.
All members in the Brisbane area are invited to attend the Annual General Meeting of
the Club at IndigiScapes, Capalaba on April 18'" next to be followed by a guided walk
through the gardens and bush area of this attractive and interesting facility. As I will
be retiring from all management committee activities at that time, your presence will
assist in the election of, and welcome to, a new BOIC president.
Best wishes Ross
Life history notes on the Blue Tiger, Tirumala hamata hamata
(W.S. Macleay, 1826) Lepidoptera: Nymphalidae ...4
Moths of Kutini-Payamu (Iron Range) National Park 2.0.0.0... eeccccsseccceseceeeeeeeeeeeeeees 8
A Summer of Butterflies 2014/2015 (aka the Year of the Tiger) .......... eee ceeeeeee eee es 14
Peacock or Green Carpenter (Xy/ocopa, formerly 1n genus LeSTIS) .........ccseecccseseeeeeeees 16
New Distribution Records for Nymphalid Butterflies (Lepidoptera: Nymphalidae)
in Queensland .............. 18
Brown Stag Beetle (Rhyssonotus nebulosuS) 1N Brisbane .............ccccccesscceeeseceeeneceeeeees 34
A Problem with Identifying Moths ........... ccc ccesscccesseccceneccceessccceesceceeesceseescceenecesenees 36
Unusual butterfly life history aberrations .............. cc ceccccssseccceececeeneccceeecceeeeecceeeneceeeeees 37
DEAT STS alee eTevads a voneclbe elevadsa oy dethetahedsnrarnOebhenedelsiterniebherabelseeesethenenedsattek «puedes te read ve Bene dle: 40
Articles from past issues - The Caper White Migration ...............cccccccsssccccesecceeseeeeeeees 40
OMSL GIrOUp Ss: ACTIVI SS 8 Sede cyto devetevleysteraslovreerd sardines sev aeerdscv dee aatidy te beesny need taboos 43
BOG EPG Cranes, cccvscdet iphone tiv aelsindtnes dvanerl edie albrreredbadn acide bended tebe’ 43
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Magazine of the Butterfly and Other Invertebrates Club #76 — Page 3
CREATURE FEATURE
Life history notes on the Blue Tiger, 7irumala hamata hamata
(W.S. Macleay, 1826) Lepidoptera: Nymphalidae - Wesley Jenkinson
This well-known butterfly species 1s
frequently encountered along much of
eastern Queensland. The adults are
migratory and can number in their tens
of thousands when this occurs. They
frequent a wide range of habitats from
rainforest to wide open woodlands and
erasslands, particularly during
migrations. It also penetrates inland
west of the Great Dividing Range into
the drier regions.
Valentine (1988) noted that “although a
specimen of the Blue Tiger was not
included in the Banks' collection, there
is a description in his journal of a vast
ageregation of butterflies which appear
to have been Blue Tigers”. He further
states that “on 29" of May 1770, when
Blue Tiger (Zirumala hamata hamata) the Endeavour was about halfway
PRO -TRGn JR SOR between (the latitudes of what
eventually became) Rockhampton and
Mackay, Banks recorded seeing ‘acres’ of them”.
The main breeding habitats are dry vine forest and littoral rainforest where the host
plants (vines in the family Asclepiadaceae) are growing. In South-east Queensland the
main hostplant 1s Secamone elliptica (or Corky Milk Vine) and although Cynanchum
carnosum (Mangrove Milk Vine) has been we, ©
listed in the past, it appears to be rarely used
(see J.T.StL. Moss comment in Braby, 2000).
In central coastal Queensland the adults
ageregate during the winter months in large
numbers in moist gullies 1n littoral rainforest
(Moss, 1995; Valentine, 1988). Here they perch ;
on dead sticks or branches and can be found in
company with other nymphalids including
Euploea sylvester, E. core and E. tulliolus.
*—t*,
Aggregation at Shoalwater July 2010
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Magazine of the Butterfly and Other Invertebrates Club #76 — Page 4
The adults fly in sunny weather and often in warm cloudy conditions and are capable
of rapid flight when disturbed. Both sexes are readily attracted to a wide range of
small native and introduced flowers and can also be observed imbibing moisture from
the ground during hot weather.
Within Queensland, individual specimens show slight variation
in the size and shape of the blue wing markings. To determine
the sexes, males have a clearly visible small protruding pouch on
the hindwing underside and a corresponding patch of grey sex
scales on the hindwing upperside.
r 4
Wingspans for the pictured adult specimens are: male 75mm and females 70mm.
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Ovipositing females flutter slowly around the host plants and settle, laying the eggs
singly, chiefly on the upperside of fresh young leaves and shoots. The wings often
remain slightly open while ovipositing occurs. Females will oviposit within
centimetres of ground level if suitable fresh leaves are available.
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Tirumala hamata hamata (Blue Tiger)
Images left to right: male, female
In January 2007, an egg was collected from near Beaudesert and
raised through to an adult on Corky Milk Vine (S. e/liptica). This
egg was barrel shaped, approximately 0.7 mm wide x 1.3 mm high,
cream with approx 21 coarse vertical ribs with very fine horizontal
lines
Freshly laid ego
In captivity the larva consumed most of the eggshell soon after hatching and fed from
the edges of soft, fresh leaves during daylight hours. It completed five instars and
attained a length of 40mm.
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Magazine of the Butterfly and Other Invertebrates Club #76 — Page 5
3 instar larva 4" instar larva
5" instar larva
The pupa, measuring 21mm in length, was located below a stem of the host plant. It
was attached with silk only by the cremaster. Under natural conditions the larvae
usually leave the host vine and pupate below a leaf on a nearby shrub or tree.
Pupa lateral view Pupa ventral view _ Pupa pre-emergence
TASATACACACASACACACACATASACALA CALA CAG
Magazine of the Butterfly and Other Invertebrates Club #76 — Page 6
The total time from egg to adult was almost one month, with egg duration 4 days,
larval duration 13 days while pupal duration was 10 days.
Within the new boundary of the Scenic Rim Regional Shire south of Brisbane, I have
records of adults from late October through to July. In this location they are more
numerous from late spring until late summer, with these broods generally flying in a
southerly direction. However, this largely relates to the timing of local rainfall
triggering fresh growth of the host plants.
Numbers of migratory butterflies in this region appeared to be declining in recent
years, probably due to habitat damage especially land clearing. Nonetheless, an
enormous sich has been occurring in South-east Queensland, starting from early
a November 2014, and which is still current in
early February 2015 (when this article was
written). This has caused much public
wonderment and comment leading to local
media coverage.
In addition a recent visit to Mt French
National Park, in the shire near Boonah, 1n
company with John Moss, resulted in the
finding of many larvae of this butterfly on
Secamone elliptica, which was 1n
abundance. We felt that this localised
breeding aggregation would have
contributed 1n part to the current general
migration.
Mating pair, male at top Acknowledgement: I wish to thank John
Moss for reviewing and amending the
manuscript to account for historical and host plant information.
Photos (except first image) Wesley Jenkinson
References:
Braby, M.F., 2000. Butterflies of Australia — Their Identification, Biology and Distribution.
vol 2. CSIRO Publishing, Melbourne.
Moss, J.T.St L., 1995. Butterfly records from Scawfell Island, Queensland, with a note on the
local form of Hesperilla malindeva Lower (Lepidoptera: Hesperiidae). The
Queensland Naturalist 33: (124-130).
Valentine, P., 1988. Australian Tropical Butterflies. Frith & Frith Books, Malanda, Qld.
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Magazine of the Butterfly and Other Invertebrates Club #76 — Page 7
ITEMS OF INTEREST
Moths of Kutini-Payamu (Iron Range) National Park -
Graham J. McDonald
Introduction
Iron Range is located on the eastern side of Cape York Peninsula, a little more than
halfway between Cooktown and Cape York, near the settlement of Lockhart River. It
contains the largest area of tropical rainforest on Cape York Peninsula. This is due
largely to the presence of a high mountain range very close to the coast. The
prevailing winds from the south-east are forced to move up the slopes causing cooling
and consequent condensation of the moisture. The soils are also quite deep and
friable, formed from metamorphic rocks rich in iron.
All of the photos were taken between June 29 and July 5, 2014. Most were taken of
moths resting on a light sheet. Light traps were set up in a different location in the
Iron Range area on seven nights, which even in “winter” never really drops below
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Fig. |
FAMILY ARCTHDAE, S/F: LITHOSITINAE
Gymnasura flavia
Cook’s Hut Campground, Kutini-Payamu (Iron Range) National Park
G.P.S. 12°42°36.6” S, 143°17°33.09” E.
Arctid moths are small to medium, usually with yellow, red, black and white colours.
Most are considered poisonous or distasteful to predators.
There are believed to be about 280 species in Australia.
Fig. 2
F: URANIIDAE, S/F: EPIPLEMINAE
Phazaca interrupta
Cook’s Hut Campground, Kutini-Payamu (Iron Range) National Park
G.P.S. 12°42’36.6” S, 143°17°33.09” E.
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Magazine of the Butterfly and Other Invertebrates Club #76 — Page 8
The Uraniidae family of moths are large to medium, mostly confined to rainforest
habitats in the north of Australia. This species is unusual in that 1t occurs 1n arid zones
as well.
This species has the unusual resting pose of rolling its forewings. The moth in the
photo also had this pose when it landed on the sheet, but then unrolled the forewings
into a normal (flattened) position.
Fig. 3
F: ARCTHDAE, S/F: LITHOSHNAE
Heterallactis phlogozona
Old Coen Walk, Kutini-Payamu (Iron Range) National Park
G.P.S. 12°44°14.43” S, 143°15’42.87” E.
This genus of arctid moths is tropical and subtropical in distribution. Most have a
yellow background wing colour traversed by red or brown bands or broad areas.
They are all small to medium in size.
Fig. 4
F: CRAMBIDAE, S/F: ACENTROPHINAE
Theila triplaga
Old Coen Walk, Kutini-Payamu (Iron Range) National Park
G.P.S. 12°44714.43” S, 143°15’42.87” E.
This colourful small moth belongs to a group of moths that have aquatic larvae.
The larvae have up to four different methods of breathing under water where they
feed on aquatic plants.
Acentrophinae are generally small to medium moths with orange, yellow, black and
white dots and bands, but some such as the common and widespread Hygraula nitens
are dull coloured.
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Magazine of the Butterfly and Other Invertebrates Club #76 — Page 9
Se Fe
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Fig. 5
F: CRAMBIDAE, S/F: ACENTROPHINAE
Parapoynx polydectalis
Old Coen Walk, Kutini-Payamu (Iron Range) National Park
G.P.S. 12°44714.43” S, 143°15’42.87” E.
This species of aquatic moth seems to have a broad distribution. I have photographed
it on several occasions at Mudgeeraba in S.E. Queensland.
Fig. 6
F: LIMACODIDAE (Cup Moths)
Hydroclada kenricki
Old Coen Walk, Kutini-Payamu (Iron Range) National Park
G.P.S. 12°44°14.43” S, 143°15’42.87” E.
Cup moths are medium to large moths with wings held steeply roof-wise at rest. The
antennal pectinations 1n the male shorten rapidly towards the tip as seen 1n the photo.
Larvae, of this group, are well known for their bright colours, slug-like shape and the
ability to sting.
Fig. 7
F: LACTURIDAE
Anticrates metreta
Iron Range Road
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Magazine of the Butterfly and Other Invertebrates Club #76 — Page 10
G.P.S. 12°44’20.86”"S, 143 °14’40.26”E.
These moths are small to medium with antennae held out in front of the head at 45”.
They have bright colours of red, orange, yellow and black.
They are mainly found inhabiting tropical and sub-tropical rainforest areas.
Fig. 8
F: SATURNIDAE
Neodipthera sulphurea
Iron Range Road
G.P.S. 12°44’20.86”S, 143 °14’40.26”E.
This family contains some of the world’s largest and most popular moths. The species
illustrated is not as large as the similar and well-known gum emperor moths and the
hercules moths.
Larvae are large and colourful with sparse hairs and fleshy turrets.
Fig. 9
F: CRAMBIDAE, S/F: SPILOMELINAE
Glyphodes actorionalis
Iron Range Road
G.P.S. 12°44’20.86”S, 143 °14’40.26”E.
The Glyphodes moths generally have transparent to translucent wing panels that
reflect a bluish or violet light.
There are about twenty recorded Australian species, many of which occur in northern
Queensland.
Fig. 10
F: GEOMETRIDAE, S/F: STERRHINAE
Antitrygodes parvimacula
Iron Range Road
G.P.S. 12°44’20.86”S, 143 °14’40.26”E.
This 1s a large species of moth found on Cape York but its range extends from New
Guinea to Babinda in Queensland.
The larvae are ‘loopers’ and probably feed on plants of the Rubiaceae family.
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Magazine of the Butterfly and Other Invertebrates Club #76 — Page 11
Fig.11
F: NOCTUIDAE, S/F: CATOCALINAE
Erebus crepuscularis
Gordon Creek, Kutini-Payamu (Iron Range) National Park.
G.P.S. 12°42754.49” S, 143°18°5.19” E.
This very large moth occurs in northern Queensland from Thursday Island to Paluma.
The similar Erebus terminitincta 1s found from Eungella to Woolgoolga, N.S.W. It
differs from Erebus crepuscularis in having a white patch on the costa of the
hindwing.
Fig.12
F: ARCTITDAE, S/F: LITHOSHUNAE
Heliosa sp.
Gordon Creek, Kutini-Payamu (Iron Range) National Park
G.P.S. 12°42754.49” S, 143°1875.19” E.
Fig.13
F: CRAMBIDAE, S/F: SPILOMELINAE
Didymostoma aurotinctalis
Portland Roads Road, Kutini-Payamu (Iron Range) National Park
G.P.S. 12°42758.74” S, 143°18735.49” E.
This is a medium sized moth and occurs 1n rainforest from Iron Range to the Cairns
area. The transparent wing panels are believed to aid in its protection from predators
BEES Pe DE DT be PED be be Pe bd be Re Pd Pe Pe bd bd
Magazine of the Butterfly and Other Invertebrates Club #76 — Page 12
by breaking up the shape of the moth, due to green leaf colours passing through the
wings.
Fig.14
F: ARCTIIDAE, S/F: ARCTIUINAE
Amerila nigropunctata
Portland Roads Road, Kutini-Payamu (Iron Range) National Park
G.P.S. 12°42’58.74” S, 143°18’35.49” E.
There are about six species of Amerila, mainly in tropical Australia, although one,
Amerila crokeri comes into northern N.S.W.
They all exude a strong-smelling acrid yellow froth, from glands near the wing bases,
if they are disturbed. This adaptation would offer protection from predators.
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Fig.15
F: CRAMBIDAE, S/F: SPILOMELINAE
Desmia discrepans
Gordon Creek, Kutini-Payamu (Iron Range) National Park.
G.P.S. 12°42’54.49” S, 143°18’5.19” E.
Fig.16
F: OECOPHORIDAE, S/F:0ECOPHORINAE
Piloprepes aemulella
Portland Roads Road, Kutini-Payamu (Iron Range) National Park
This 1s a small to medium brightly coloured moth that comes from a very large family
of usually drab moths
It was finally photographed after a long chase through heath and open savannah
woodland.
Photos Graham McDonald
References:
Common, I. F. B. (1990) Moths of Australia Melbourne University Press
Richardson, B. (2008) Mothology: Discover the Magic LeapfrogOz
Zborowski, P. and Edwards, E. D. (2007) A Guide to Australian Moths CSIRO Publishing
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Magazine of the Butterfly and Other Invertebrates Club #76 — Page 13
A Summer of Butterflies 2014/2015 (aka the Year of the Tiger) -
Peter Hendry
While it does not fit with the Chinese calendar, this summer, in S. E. Queensland,
could be described as the Year of the Blue Tiger (7irumala hamata hamata).
Everyone I know has noticed them this summer. Our own president, Ross, has been
on the TV news reporting on them and Robert Ashdown has just posted on the club’s
Facebook page, images of numbers of Blue Tigers nectaring on his Ivory Curl Tree
(Buckinghamia celcissima). My brother, Quentin, rang last Saturday, 31/01/2015,
reporting he could not count fast enough to keep up the number of Blue Tigers flying
through his property, just south of Childers. Good rain has produced lots of fresh new
erowth for the larvae to feed on and has increased the numbers of butterflies across
the range. But why so many Blue Tigers’?
Fig.1 Blue Tigers aggregating
Photo Pam Thompson
Blue Tigers are known to aggregate
overwinter with the females dispersing in
spring. Evidence of such aggregations was
provided to me by Pam Thompson, a friend
of my brother, in an image, (Fig. 1), taken
on the Bargara/Mon Repos trail on 7th July
2014. While I have no information on the
numbers present, based on the image they
must have been in their hundreds. Also
present in the image is the odd Common
Crow (Euploea core). It is the females
from such overwintering sites combined
with lots of rain-driven fresh new growth
on their host plants, mainly Corky Milk
Vine (Secamone elliptica), that has
provided us with such a spectacle of Blue
Tigers over this summer.
Blue Tigers are not the only butterfly to
benefit from this season’s summer rains.
A phone call from club member Richard
Zietek, informing me he had seen a Four-
barred Swordtail (Protographium leosthenes) 1n his yard at Capalaba, sparked my
interest. I live in the adjoining suburb of Sheldon and had only once seen a Four-
barred Swordtail here and as I was planning a trip to my bush block, west of
Bundaberg, where I had seen Swordtails in numbers once before, things were looking
good. The following week a Swordtail made an appearance here at Sheldon and over
the summer | have had two other visitors.
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Magazine of the Butterfly and Other Invertebrates Club #76 — Page 14
The trip to my bush block proved eventful. Accompanied by my brother, skirting
around the northern side of Good Night Scrub, expecting, as on previous occasions, to
see a few butterflies mud puddling, we were stopped in our tracks. Hundreds 1f not
thousands of Yellow Albatrosses (Appias paulina) were mud puddling along the side
of the road (Fig. 2). From there until we reached our block, on the Perry River,
:
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Fig. 2 Yellow Albatrosses (Appias paulina) mud puddling along the side of the road
Photo Peter Hendry
everywhere there was a puddle there were Yellow Albatrosses. Noticeably 99% of
them were males (Fig. 3) with only the occasional female. As for Four-barred
Swordtail, on the whole of the trip including the return trip the total numbered was
seven, six on the block and one coming home. Yellow Albatrosses were dominate,
for every Blue Tiger, a hundred Yellow Albatrosses, for every common Crow a
hundred Yellow Albatrosses. They were even mud puddling on the edge of the Perry
River at the bottom of our block. Ona
walk down to the River we were amazed
at the number of larvae, mostly moth
larvae, feeding on all the trees. I
collected some Opodiphthera astrophela
larvae feeding on both Crows Ash
(Flindersia Australis) and Red Ash
(Alphitonia excelsa), a moth I had not
recorded from the block before.
ea || Meanwhile back at Sheldon the Blue
| ‘. | Tigers while not in large numbers are
PEE ae SOM: RUS more numerous than any other year I can
Photo Peter Hendry
remember. Unfortunately there is no
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Magazine of the Butterfly and Other Invertebrates Club #76 — Page 15
evidence that they have found my Secamone elliptica, which remains uneaten.
Yellow Albatrosses are also present and have taken up residence in the back yard
where they enjoy hiding amongst the trees. While they have been here in the past I do
not see them every year. I have three specimens of their host plant Drypetes
deplanchei but for some inexplicable reason none have produced new growth this
summer and I have found no evidence of the Yellow Albatross breading.
The Common Crow is here as usual but not in any increased numbers. One has just
laid an egg on my wife’s new Dwarf Frangipani (Plumeria pudica) - best I not tell her
- interesting to see if it goes through. The Plumbago Blue (Leptotes plinius) has
increased in numbers, hundreds of them, with their exotic host plant, Plumbago
auriculata, now covering about 10m? and the native Plumbago zeylanica running riot
along the ground, they have plenty to feed on.
Other butterflies I have seen here in increased numbers this summer are the Blue
Triangle (Graphium sarpedon) and the Orchard Swallowtail (Papilio aegeus), though
mostly males. It 1s hard to say 1f the Lemon Migrant (Catopsilia pomona) 1s in
increased numbers but there are plenty here. In lesser numbers have been the Pale
Triangle (Graphium eurypylus), though I have seen a yellow morph and the Purple
Crow (Euploea tulliolus), of which I only ever have a few but to date only two.
oe Se ee
Peacock or Green Carpenter (Xylocopa, formerly in genus Lestis) -
Erica Siegel
Xylocopa bombylans is found along the coast from Sydney to Cape York and
X. aeratus 1s found around Sydney, on the Dividing Range up to approximately the
Stanthorpe area.
The female of these spectacular bees is a
glossy metallic blue with purple tints
and the male a metallic green with
yellow tints. Peacock/Green Carpenter
bees are 13 to 20mm long.
The face of the female Xylocopa
bombylans has green and white hairs.
Males of X. bombylans have white
markings while males of X. aeratus
have yellow face markings.
With their mandibles Peacock Carpenter
bees cut 7 to 10mm wide nest burrows
in the flower stalks of grass trees
(Xanthorrhoea) or in the soft pithy dead Female Xylocopa bombylans
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Magazine of the Butterfly and Other Invertebrates Club #76 — Page 16
timber of Banksia, Tristania, Acacia, Leptospermum and Casuarina. The Peacock
Carpenter bees remove excavated wood from the nest by sticking the end of their
abdomen out of the entrance hole and then, with their legs, throwing out the wood
particles.
They make rounded cells for their eggs. Each cell 1s stocked with pollen and nectar
formed into “bee bread” before the female lays a large egg on top. She then closes the
cell with a plug of chewed wood particles.
According to Dr.Katja Hogendoorn ( University of Adelaide) the emerged young bees
are fed in the nest and take quite some time before venturing out of the nest. I have
observed them placing their abdomen into the entrance hole to excrete digested meals
to the outside so not to soil the nest.
The nest burrow may be shared by males and females to help guard the nest.
Peacock Carpenter bees are buzz pollinators and “buzz pollinate” by grasping the
flower and vigorously vibrating their flight muscles, thus sonicating the flower. This
1s important for flowers where the pollen 1s trapped in narrow tubes. Peacock
Carpenter bees are attracted to flowers needing “buzz pollination” such as Hibbertia
scandens, Melastoma affine and Solanum jasminoides. They also forage in Pea
flowers like native Pultanea sp., Gompholobium sp.,and other natives such as
Eriostemon australasius, ( Pink Wax Flower) Leptospermum, Macadamia, native
Wisteria, Senna sp., Leucopogon as well as exotic Cuphea among others.
Nectar-foraging Peacock Carpenter bees often pierce the corollas of long-tubed
flowers, and thereby reach the nectar without contacting the anthers. Such “nectar
stealing” has been observed for_X. bombylans feeding on Cuphea sp.. This would lead
to a reduction in pollination.
When foraging among flowers the Peacock Carpenter bees emit a deep droning sound
and are therefore easily located.
Land clearing has caused the loss of these stunning bees from Victoria and mainland
areas of South Australia although they can still be found on Kangaroo Island in South
Australia.
Photos Erica Siegel
References:
Dollin A. Australian Native Bee Research Centre www.aussiebee.com.au
Dollin, A., Batley, M., Robinson, M. & Faulkner B. Native Bees of the Sydney region, a field
guide — Australian Native Bee Research Centre.
http://www.adelaide.edu.au/directory/katja.hogendoorn
http://en.wikipedia.org/wiki/Xylocopa bombylans
http://www.padil.gov.au/pollinators/
http://australianmuseum.net.au/Peacock-Carpenter-Bee
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| BS iP”
Figs.1 and 3 Peacock Carpenter bee (Xylocopa bombylans) female
Fig. 2 Peacock Carpenter bee male Fig.4 Ejyecting wood particles
oe i
New Distribution Records for Nymphalid Butterflies (Lepidoptera:
Nymphalidae) in Queensland - Kelvyn L. Dunn
Summary
This paper documents 53 new locations in inland, outback and central Queensland,
Australia, for 17 species of nymphalid butterflies. Each record is from a location that
falls outside the boundaries of the species’ distributions, as indicated on the range-
filled maps provided by Braby (2000). The report also discusses relevant new
locations discovered by others since 2000, namely those that lie close to any listed in
this paper, but in doing so it does not reiterate historic distributions that underpin
Braby (2000). The many new locations for the species tabled provide ongoing
evidence that there remains much to learn about butterfly species’ distributions,
especially in western Queensland.
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Introduction
Those insect enthusiasts who occasionally visit remote areas of Queensland may pay
little attention to the nymphalid butterflies a group comprising a number of
subfamilies whose members are usually very conspicuous on the wing. The casual
naturalist, familiar with butterflies and when equipped with a suitable field guide, can
readily identify most of those seen at close to moderate range, as many of the species
have striking differences. Others, so inclined, with a growing field expertise can
effortlessly photograph the adults and easily identify them by this means, or may
choose to seek assistance to that end from those with more experience. Photography is
easiest when adult butterflies pause to feed at flowers or when they roost on low
foliage in the evenings or, at other times, during unsuitable weather for sustained
flight. Both means of data gathering will provide quality records for the species that
occur 1n Queensland, save some from a few complex groups like the Crow butterflies
where specimens may be required, particularly in the far north of the state, to
eliminate doubt that may arise at times.
Regular observations by casual observers have built up a substantial knowledge of the
distributions of nymphalid butterflies because their members, like those of the
Swallowtails (Papilionidae) and Whites and Yellows (Pieridae) (see Dunn 2013a, &
2014 for complementary pieces on these groups), are conspicuous 1n areas where they
occur. Despite their moderate size and visibility, the known distributions for some of
the more widespread and common species are still patchy, fragmentary, and likely
under-representative beyond the coastal and sub-coastal regions where most butterfly
fieldwork is repeatedly done (Dunn 2010). That paucity of knowledge applies
especially to species that periodically disperse inland along major river systems (from
moister upland regions of the western slopes of the Great Dividing Range in eastern
Australia), or from floristically richer regions nearer the eastern coast after traversing
the range. It 1s possible that Yoma sabina (the Lurcher) 1s one of those species that
expands inland along river systems (to a limited extent) during the wet season (or
farther afield in those more favourable years) where at other times it 1s less likely to
be found, or is not present. At such times, it may breed seasonally or opportunistically
on plants belonging to the family Acanthaceae to create meta-populations. The
surprising record of this species in the Chillagoe area, notably distant from other
eastern locations, would support this suggestion, but adults have been seen only at
limited times of the year, albeit often commonly. Garry Sankowsky (p.c. 2014) who
knows the area informed me that, ““The main host plant there 1s Dipteracanthus
australasia and it is quite abundant in most of the vine thickets on the bluffs all
around Chillagoe. They also use Brunoniella australis which grows outside of the
vine thickets, but Yoma does not venture too far from the vine thickets/rainforest.”’
Methods
During several lengthy field trips through inland and northern Queensland (see Dunn
2013b for map of sites visited in 2011 & 2012), I pragmatically recorded Nymphalids
(and all other butterflies) 1n order to help alleviate the knowledge imbalances that
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exist for the inland of northeastern Australia (Dunn 2009, 2010). I utilised a roadside
explorative approach that involved examination of numerous sites along major inland
highways and byroads, on route to and from the Gulf Country in 2011-12 and to and
from southern Cape York Peninsula, along the coastal route, in 2001-02. I chose sites
according to the various types of habitat available and where these habitats showed
less human disturbance, 1n order to maximise the number of species seen. The
procedure involved slowly walking through each site visited (often involving a 15-30
minute inspection), and in process listing all species encountered that could be
positively identified by various means (netting, photography and close visual
observations) on all four trips. Most inspections occurred between 0900 and 1730h
(AEST) each day for the entirety of each trip, usually irrespective of the weather (if
only marginally unsuitable) as adults might still be found by disturbing them from
roosting sites, but with an obvious focus on sunnier periods to maximise encounter
rates with adults (the main life stage sought).
I identified many of the adults seen without the requirement of handling; least
interference has been the option aimed for over the years, where the record was
thought (at the time) to be mundane. Those forty (40) encounters (65.6%) recorded by
‘observation-only’ are marked (Obs.). For 39 (97.5%) of these observations the
identifications were certain (Category 1). In each case, I recognised sufficient
characters to achieve that level of confidence. Only one observation was to a level of
‘almost certain’ (Category 2) as the field circumstances did not permit sufficient time
and closeness to identify the species to a level beyond reasonable doubt on that
occasion (see Dunn 2011 for discussion of this category and other categories of record
acceptability). That particular record (which involved Junonia orithya) 1s marked
‘C2’ to distinguish it as less reliable as observations go; nonetheless the new
distribution it suggests is well supported by neighbouring records (see Table and a
relevant reference linked to the species concerned) so there seems little concern by its
inclusion.
I retained voucher specimens at times (where this was permissible and achievable),
and more often than not, these were taken from locations where the species concerned
were far beyond their known ranges. For that reason, the percentage of vouchers in
the Table (24.6%) is higher than the usual frequency for all records on the trips
concerned (because the table is selective data and lists only those records that
represent new locations). Sometimes vouchers ought to have been taken to help
improve the survey rigour, when in fact they were not; the main reason being was that
on many occasions I did not recognise that a particular location was evidence of new
distribution at the time of the field encounter. Occasionally too, a compromise was
struck, and some adults suspected of being from new or perhaps cusp locations were
caught and examined to confirm their identification (to strengthen a record that might
be challenged) and then released (Rel.) (4.9%). A very small portion of records was
photographed in the field (4.9%) where this was practicable; these serve as supportive
evidence that can be examined by others, should this be required (some are
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reproduced in this report to substantiate those encounters). At times too, I also
retained adults that had posed for video photography (the imagery means utilised), if
they lingered unduly (but oftentimes they would quickly depart on my closer
approach); these are included among those marked as vouchers, but each includes a
superscript-link to the photos (video frames) concerned. Records that standalone as
image-only (meaning the specimens were not retained as vouchers) are marked as
‘Photo’ (0.6%).
The method used to measure distances, and define locations to precision of within a
kilometre of the actual site, has been described previously (Dunn 2013c); extended
discussion and other recommendations to help describe locations effectively and, in
process, to avoid ambiguity are detailed elsewhere (Dunn 2013d) and not reiterated.
Results and Discussion
The table lists 61 records of 17 species from 53 new locations (arranged from north to
south), across Queensland; all sites fall outside the boundaries defined by Braby
(2000) for the species concerned and so are new on that criterion. References to
findings of other workers in the last decade or so are cross-linked where their
published new locations fall close to those listed. For Melanitis leda the new record
from the Gulf Country hinterland provides evidence of what may be a continuous
distribution through the coastal region of northern Australia. Similarly, the records of
Mycalesis perseus, Charaxes sempronius, Acraea andromacha, Junonia orithya, J.
hedonia, Danaus plexippus and D. affinis from the greater Normanton district add to
available knowledge and 1n doing so, each helps bridge the gap in the eastern Gulf
Country for these common and widespread species. The central Queensland record of
Pantoporia consimilis was a surprising southern encounter (in a region that has been
well examined previously), and one that seriously challenged my predatory stealth (in
absence of the proverbial net) as I homed in to photograph the single adult, which was
basking 1n a sunlit vine thicket. The dense tangle of vines which treading upon
immediately disturbed higher foliage in the vicinity, alerted it as to my approach each
time, and prompted a routine leisurely glide, with intermittent flutter, back and forth
in the small glade. It remained site tenacious and often chose to perch at a moderate
height, which when I was eventually close to it was just a little too high above my
head for a suitable view from below — a stepladder would have been handy!
For the other nymphalid species, some of the extensions recorded may be minor but
each provides evidence of a broader inland occurrence in the area concerned. Most of
these new records link in to an inadequate knowledge of species’ distributions — due
to a lack of regular exploration of the inland by insect enthusiasts (collectors and
photographers) — rather than because of unusual or localised climatic conditions that
were present in southeastern Australia for some of the years concerned. Each record
adds insight into the distribution of those species of butterfly in the inland,
particularly the Gulf Country where much effort focussed, and helps fill knowledge
gaps evident in their distributions (as based on the range-fill maps in Braby 2000).
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Acknowledgements
I sincerely thank Garry Sankowsky (Queensland) for detailed biological information
on Y. sabina in the Chillagoe area, and for permission to include his observations in
this report to supplement my own records. I also thank Dr Russell Best (Victoria
University, Vic.) for identifying (based on photos of flowers and foliage) the nectar
source of H. metirius at Carnarvon Gorge.
References:
Atkins, A.F., Edwards, E.D., Braby, M.F., Johnson, S.J. & Valentine, P.S. 2003. The butterflies of
White Mountains National Park, northern Queensland, and adjoining localities. /n
Comben, L., Westacott, T. & Berg, K. (eds). White Mountains Study Report. Geography
Monograph Series No. 9. (pp.7-10). The Royal Geographic Society of Queensland Inc.
Brisbane. 1v+146pp.
Braby, M.F. 2000. Butterflies of Australia: their identification, biology and distribution.
CSIRO Publishing, Collingwood Vic.
Braby, M.F. 2014. Remarks on the spatial distribution of some butterflies and diurnal moths
(Lepidoptera) in the Top End of the Northern Territory, Australia. Northern Territory
Naturalist 25: 29-49.
Daniels, G. & Edwards, E.D. 1998. Butterflies from Lawn Hill National Park and Musselbrook
Reserve, Queensland. /n Comben, |., Long, S. & Berg, K. (eds.). Musselbrook Reserve
Scientific Study Report (pp.89-91). The Royal Geographic Society of Queensland,
Brisbane.
Dunn, K.L. 2009. Overview of the butterfly database: Part 2 — Current composition, imbalances
and factors of influence. Victorian Entomologist 39(5): 89-100.
Dunn, K.L. 2010. Overview of the butterfly database: Part 4 — Personal contributions (KLD).
Victorian Entomologist 40(5): 98-109.
Dunn, K.L. 2011. Overview of the butterfly database: Part 6 — The knowledge gap,
identification complexity and measures of record acceptability. Victorian
Entomologist 41(2): 30-38.
Dunn, K.L. 2013a. New distribution records for Swallowtail butterflies (Lepidoptera:
Papilionidae) in eastern Australia. Metamorphosis Australia, Magazine of the
Butterfly & Other Invertebrates Club 70: 8-14.
Dunn, K.L. 2013b. Field Notes: Major extensions to the known distribution of the Bright Purple
Azure, Ogyris barnardi (Miskin 1890) in Queensland (Lepidoptera: Lycaenidae).
Metamorphosis Australia, Magazine of the Butterfly & Other Invertebrates Club 68:
26-32.
Dunn, K.L. 2013c. Field Notes: Gulf Country extensions to the known distribution of the Long-
tailed Pea-blue, Lampides boeticus (Linnaeus 1767) in Queensland (Lepidoptera:
Lycaenidae). Metamorphosis Australia, Magazine of the Butterfly & Other
Invertebrates Club 69: 17-23.
Dunn, K.L. 2013d. Overview of the butterfly database: Part 7 — Descriptions of provenance and
promotion of new trends. Victorian Entomologist 43(1): 13-22.
Dunn, K.L. 2014. New distribution records for Sulphur and White butterflies (Lepidoptera:
Pieridae) in inland and outback Australia. Metamorphosis Australia, Magazine of the
Butterfly & Other Invertebrates Club 75: 14-25.
Dunn, K.L. & Dunn, L.E. 1991. Review of Australian butterflies: Distribution, life history and
taxonomy. Parts 1-4. Melbourne, Australia: Published by the authors.
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Magazine of the Butterfly and Other Invertebrates Club #76 — Page 22
Franklin, D.C. 2007. Dry season observations of butterflies in the ‘Gulf country’ of the Northern
Territory and far north-west Queensland. Northern Territory Naturalist 19: 9-14.
Kendall, R. 2011. A new location for the Dusky Knight, Ypthima arctous (Fabricius, 1775)
(Lepidoptera: Nymphalidae: Satyrinae). Metamorphosis Australia, Magazine of the
Butterfly & Other Invertebrates Club 63: 33.
Monteith, G.B. 1971. Insect collecting at Iron Range. News Bulletin of the Entomological
Society of Queensland 78: 17-20.
Pierce, F. 2008. Range extension records for various butterflies throughout Australia. Victorian
Entomologist 38(1): 15-16.
Valentine, P.S. & Johnson, S.J. 2000. Butterflies of southwestern Queensland with life history
notes. Victorian Entomologist 30(5): 59-62.
Valentine, P.S. and Johnson, S.J. 2001. Observations of butterflies at the Carnarvon Range,
Queensland. Victorian Entomologist 31(1): 2-3.
Key to Table:
Note 1. A solitary adult of Melanitis leda, in fairly worn condition and closest in
fascies to the dry season form, was flushed from undergrowth in paperbark
gallery forest, between 1255-1335h AEST (the duration of survey). Once
startled, it flew rapidly but quickly sought shelter amongst leaf litter 1n an
area of deeper shade farther afield, whereafter 1t was not seen.
Note 2. During three differently timed visits (one in mid-late morning, one in mid-
afternoon and another in late afternoon), I walked extensively along the
northern riverbank in search of satyrine butterflies. A few aged females of
Mycalesis perseus were encountered in vine thickets in mid and late
afternoon, and another was seen in the morning the next day, which provided
evidence of at least one species hitherto unrecorded from the eastern Gulf
Country. However, I did not find evidence of M. terminus at this location, a
riparian site where I thought the species might occur if suitable larval food
plants are present. Braby (2000) expressed doubt concerning the authenticity
of the single male specimen of M. terminus from Normanton in the ANIC,
which Dunn and Dunn (1991) had included in the species’ distribution.
Braby (2000 p.477) reported that the specimen concerned was “collected by
J.C. Le Souef’. I had examined the specimen when it was held in the Le
Souef collection at Blairgowrie, and recorded that a certain ‘R. Howard’ (not
Le Souef) had collected 1t on 5 August 1958 (and, from memory, that it was
labelled in Le Souef’s handwriting). Data-matching (using Dunn & Dunn
database) suggests that R. Howard collected at Mount Isa on the two
previous days in August, but there 1s no evidence (from surviving specimen
labels) of his subsequent journey from the Gulf. If he had then travelled to
the eastern coast of Queensland this could explain its origin, assuming the
label data is mistaken. The M. terminus record does seem doubtful (there is
no other evidence of it from the Gulf area at this time), but there might be
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suitable habitat about greater Normanton where the species could exist;
hence Braby’s call for confirmation still stands.
Note 3. There were a few adult Ypthima arctoa flying 1n a vacant residential block in
the main street between 1255 and 1400h AEST, at 20°46°10”S,
145°01°16”"E; some were seen to feed at flowers of Tridax procumbens
(Asteraceae) growing near a water tank. I was a little surprised to see this
butterfly 1n the township (where it was locally common) as none had been
seen in the woodland areas inspected in the Prairie district to the west, nor
(later) in the woodland in the Burra Range area to the east. Nonetheless, the
species occurs in the nearby White Mountains National Park (Atkins et al.
2003), and within which the Burra Range is included, and it has, on one
occasion, been taken farther west at Koon Kool (station), 25km NE of
Hughenden (Kendall 2011).
Note 4. A male Hypocysta metirius was photographed feeding repeatedly at flowers
Note 5.
of Lobelia trigonocaulis (Campanulaceae), at 1540h AEST (Figure 2 & 3),
alongside feeding adults of H. pseudirius (Figure 4), a species very similar in
appearance. Both species were localised and co-occupied the same shady
areas 1n riparian grassy woodland where they perched on low foliage, but the
flight of H. metirius 1s switter, which drew my attention to it for a closer
inspection. H. metirius occurs elsewhere in the Carnarvon Range, “some
95km south of Rolleston, 75km north of Injune” at 25°14.6’°S, 148°37.6°E
(Valentine & Johnson 2001) but was hitherto unknown from the Carnarvon
Gorge.
In the Gulf Country of western Qld, Charaxes sempronius has been recorded
at Hedleys Gorge and Hells Gate Roadhouse (Franklin 2007); the new
encounter adds to these earlier reports and provides for a_ broader
distribution.
Note 6. A small male C. sempronius was seen to feed at sandy mud (near the water’s
edge) on a large sandbar in the Flinders River at 1325h AEST. I have not
seen this species seeking nutrients at mud before (that I can recall), but
because of the presence of large crocodile tracks which led directly to the
waters’ edge, near where the butterfly was, I did not linger unnecessarily in
the area for a timely photograph to capture this interesting behaviour.
Instead, I swiftly netted the adult (using a net with a long extendable handle)
and subsequently placed the butterfly on wet sand under artificial lighting
that evening; he commenced to feed again and so posed for the photograph
provided herein (Figure 6), suitably representative of the actual activity
observed in the field that day.
Note 7. This cusp record of Acraea andromacha 1s certainly not the first from the
Lawn Hill area but is additional evidence of the species’ presence at or near
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Note 8.
the western boundary of its irregular occurrence (as estimated from the
synoptic map presented by Braby (2000)). Daniels and Edwards (1998) listed
it from Lawn Hill National Park and Musselbrook Reserve, and more
recently, Franklin (2007) encountered it in the “Main Gorge area’ of Lawn
Hill N. P. The species may be regular (rather than irregular) 1n the Lawn Hill
region.
An adult of A. andromacha was seen roosting 1n shade on a small rocky knoll
in shrubby woodland, during very hot weather (between 1505 and 1525h
AEST), judged as “probably 40°C” according to my field note book; it
reached 39°C in Mt Isa that day.
Note 9. This encounter adds to the earlier report by Pierce (2008) who recorded the
Note 10.
species at Fullarton (as “Fullaton’) River, west of Julia Creek (township).
This record of A. andromacha 1s not the first from this area but is additional
evidence of its presence; Atkins et al. (2003) included the species in a list
from the Warang Homestead area and nearby gorges of the White Mountains
National Park, marginally to the east. Atkins’ personally surveyed during a
scientific expedition in April 2000 (and recorded the species on that
particular visit), but that paper included records of this species from other
visits (attributed to three other workers), which came from either the gorge
area or Burra Range, or both.
Note 11. Several adults were seen to feed at a large ‘cedar tree’ in parkland, near an
Note 12.
entrance to a caravan park, between 1215 and 1230h AEST. It is possible
that the ornamental garden tree in the camping area, which served as a nectar
source for this and other species, was a native; and if so, it may have been a
White Cedar, Melia azedarach (Meliaceae). Queenslanders might
generically call such a ‘cedar tree’ (the name provided locally), but I did not
take any photos of the flowers to enable a reliable identification by a
botanical expert. This encounter adds to the earlier report by Valentine and
Johnson (2000) who recorded the species on Baldy Top Lookout, 5km west
of Quilpie, a location that provided a considerable westward extension of
range (and 1s west of this record from the township of Charleville).
Two adults of Neptis praslini were seen on the summit (one was taken). This
encounter adds to the earlier report by Monteith (1971) who recorded the
species from Coen; Braby (2000) referred to that information informally (by
contributor name only). Mount White, which is situated to the southwest of
Coen, is a cusp location based on its meridian of longitude; 1t appears to be
just on the outer edge of the range-fill area, as estimated from the synoptic
map provided by Braby (2000) and is important in defining the western
limits (as known at this time) on Cape York Peninsula.
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Note 13. This is a cusp record, marginally outside the distribution figured by Braby
(2000), and 1s important in defining the western limits in Dawson region,
central Qld.
Note 14. This cusp location 1s just outside the range-fill area on the synoptic map
provided by Braby (2000) and is arguably new on that reasoning. Curiously,
I cannot find a record of Doleschallia bisaltide in my field notes from this
location (written on the day concerned), nor do I have a photo or video
footage of it, but it is included in the database and was presumably this
species. It may have been preserved in ethanol and could be in the VAIC,
Bundoora or ANIC, Canberra. As the larva was not reared, and a said,
‘voucher’ is currently unaccounted for (perhaps lost now), I call for visiting
enthusiasts to gather further evidence of the species at or near this location
and from elsewhere on western Cape York Peninsula to improve knowledge
of this species’ northern distribution.
Note 15. Three adults were seen in vine thicket on the southern side of the road, more
finely, ‘about 4.5km’ (measured by road) from Chillagoe. Details of the
underwing markings, which were not recorded in my field notes (and may
not have been seen), are unclear; it is likely they resembled those adults from
the Wet Tropics region, which are usually dark (unlike some I have seen in
the hinterland of Cape York Peninsula, which have a prominent pale band).
This report is not the only one I know of from the area; G. Sankowsky has
seen the species at a number of sites in the Chillagoe region, for example,
and recently provided evidence of an adult in a video of overwintering Crow
butterflies circulated among members of the BOIC. I contacted G.
Sankowsky and he kindly supplied information on the species regularity in
the area: “The Lurcher is quite common at Chillagoe in the wet season ...
(particularly) 1n the vine thickets on the limestone bluffs. In February they
can usually be seen at any bluff where the host plant grows.” He reported the
species occurs as far west as 3km SE of Mungana at 17°08.5’ 144°25.5’
(which extends the distribution farther west than does my record).
Note 16. Pierce (2008) earlier recorded Junonia orithya from Karumba. My records,
which include encounters at Walker Creek and near the Wondoola airstrip
(as per the table) collectively support that previously published location and
another from the Flinders River crossing, south of Normanton, reported in
the same paper.
Note 17. This western record of J. orithya, albeit well outside the distribution
indicated on the synoptic map presented by Braby (2000), is not the first
from the Lawn Hill area but is additional evidence of the species presence in
the eastern Gulf Country. Daniels and Edwards (1998) listed it from Lawn
Hill National Park and Musselbrook Reserve, and subsequently, Franklin
(2007) finely recorded it from the ‘Main Gorge area’ (Lawn Hill N. P.).
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Elsewhere in western Qld, Franklin (2007) listed it from the Nicholson
River, and more remotely to the south, along a tributary of the Thorntonia
River.
Note 18. Pierce (2008) recorded J/. orithya from the Burke & Wills Roadhouse; the
new records from this general area (Table 1) are supportive of his earlier
report and considerably expand upon it.
Note 19. One adult of Danaus affinis fed in company with a female of Ogyris
amaryllis (Lycaenidae) at a red flowering bottlebrush (Callistemon sp.
perhaps viminalis) in parkland/residential area, at 1150h (AEST).
Note 20. A single adult was seen at the ‘40km roadside marker’ (which, based on the
GPS reading to seconds, obtained at the site with a hand-held device
measured 39.6km by road on Google Earth (Google Inc.)). Since my
encounter in October 2012, which was the first for the Gulf Country of
northwestern Qld, Braby (2014, p.38) has recorded the species from six more
sites in the region, during May 2013, and remarked that, “at Karumba, QLD,
many adults were seen’. Current evidence suggests the species is vagrant to
the Gulf Country.
Note 21. Although Euploea corinna is a widespread species in the inland in western
Qld, this cusp record, which is marginally outside the distribution figured by
Braby (2000), importantly helps define the western limits at this latitude in
the Thomson region.
Note 22. This is a cusp record, marginally outside the distribution figured by Braby
(2000), and 1s important in defining the western limits in the Warrego region.
Table - 53 new locations for species of Nymphalidae from beyond their known
ranges in Australia
Species/Location State Geocode Date Format
Melanitis leda
Gregory River crossing, Qld 18°39’S, 139°15’E = 10 Oct 2012 Obs “fe!
at Gregory Downs
Mycalesis perseus
Walker Creek crossing, Qld 17°28’S, 141°11V7E 3=—- 13 Oct 2012 Voucher \°?
28km NNE of Normanton 14 Oct 2012 Obs
Ypthima arctoa
Torren Creek (township) Qld 20°46’S, 145°017E =. 28 Oct 2012 beens’
ote 3, Fig
Belyando Crossing Qld 21°32’S, 146°S517E =06Nov2011 Voucher
Hypocysta metirius
Carnarvon Gorge, Carnarvon Qld 25°03’S, 148°13"E 11 Nov 2011 — Photo
NP at 25°03’03’’ 148°13’00”’ Note 4, Fig 2&3
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Hypocysta pseudirius
Tambo, in hotel rear garden
Augathella, at Warrego River
ford at 25°47°43” 146°34’48”
Tregole NP, in car park
Charaxes semprontius
Lawn Hill NP, Constance
range at summit lookout
Flinders River, at 60km
SSW of Normanton
Wyandra (in hotel rear
garden off Warrego Street)
Ikm S of Cunnamulla
(at van park)
A, andromacha
Normanton, at drain near
Travers Street
Walker Creek crossing, 28km
NNE of Normanton
Lawn Hill Creek, Adels Grove
Lawn Hill NP, Constance
range at summit lookout
8km NW by N of Quamby
Hotel, on hill top
15 km W of Julia Creek
Cloncurry Apex Lookout, 2km
W of Cloncurry
Cloncurry River anabranch,
at [km W of Cloncurry
Bottle Tree Lookout, 58km
NE of Hughenden
Wyandra (in hotel rear
garden off Warrego Street)
Augathella, at highway junct.
1.6km NE by E of Charleville
Pantoporia consimilis
Hann River roadhouse, at
bridge
Olsens Cave, 3km ENE
of The Caves
Neptis praslini
Mount White, near Coen
Phaedyma shepherd
Palm Tree Creek, at 19km
N of Taroom
Comet, Leichhardt Tree Park
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
24°53’S, 146°15’E
25°48’S, 146°35’E
26°30°S, 147°08’E
18°42°S, 138°30°E
18°10°S, 140°5 VE
27°15’S, 145°59°E
28°05’S, 145°41VE
LT°41?S, 141°04°E
17°28°S, 141°1 VE
18°41°S, 138°32’°E
18°42°S, 138°30°E
20°19°S, 140°1S°E
20°40’S, 141°36’E
20°42’S, 140°29°E
20°42’S, 140°30°E
20°28°S, 144°24°E
27°15’S, 145°59°E
25°48’S, 146°36’E
26°24’S, 146°15°E
15°12°S, 143°52’°E
23°10°S, 150°29°E
13°58’S, 143°117E
25°30’S, 149°47°E
23°33’S, 148°32’E
26 Oct 2011
Ol Oct 2012
30 Sep 2012
25 Oct 2012
12 Oct 2012
27 Sep 2012
27 Sep 2012
14 Oct 2012
14 Oct 2012
23 Oct 2012
24 Oct 2012
25 Oct 2012
16 Oct 2012
22 Oct 2012
08 Oct 2012
08 Oct 2012
22 Oct 2012
28 Oct 2011
27 Sep 2012
O01 Oct 2012
30 Sep 2012
11 Jan 2001
O05 Nov 2012
06 Jan 2002
14 Nov 2011
08 Nov 2011
es
Voucher “8°
Voucher
Obs
Ob S Note 5
Voucher
Note 6, Fig 6
Obs
Obs
Rel
Obs
Obs
Obs
Ob S Note 7
Obs
Obs Note 8
Obs Note 9
Obs
Obs
1
Voucher 4° 1°
Obs
Obs
Voucher *°t* !!
Obs
Obs
12
Voucher \°*
Obs
1
Voucher *°* !°
PEPE PE DS PF DE Pe PE DS De RE be Pe be pe Pe bd Pe bd
Magazine of the Butterfly and Other Invertebrates Club #76 — Page 28
Doleschallia bisaltide
Myall Creek crossing (Pax
Piel Bridge) 55km ESE of
Weipa
Yoma sabina
Little Laura River crossing,
12km WNW of Laura
Skm SE of Chillagoe
Junonia orithya
Brannigan Creek,
at 31km E of Karumba
Walker Creek crossing,
28km NNE of Normanton
Flinders River, 21km
W of Wondoola airstrip
Lawn Hill Creek, Adels Grove
Lawn Hill NP at
18°42’05” 138°29’°24”
Lawn Hill NP at
18°41759" 138°29’39”
Indarri Falls Lawn Hill NP
Lawn Hill NP at
18°43’04” 138° 2859”
5S5km NW by W of Burke
& Wills Roadhouse
38km WNW of Burke & Wills
Roadhouse
Burke & Wills Roadhouse
Dismal Creek crossing, 4km
ESE of Burke & Wills RH
Junonia hedonia
Walker Creek crossing, 28km
NNE of Normanton
Danaus affinis
Ikm NE by N of Karumba
Point boat ramp
Walker Creek crossing, 28km
NNE of Normanton
Normanton, in Simpson St
6km ENE of Burketown,
at creek
D. plexippus
40km NNE of Burke & Wills
Roadhouse
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
12°39°S, 142°10°E
15°32°S, 144°21°E
17°11°S, 144°33’E
17°27°S, 141°07’E
17°28’S, 141°1 VE
18°34°S, 140°43°E
18°41°S, 138°32’°E
18°42°S, 138°29"E
18°42°S, 138°30°E
18°43°S, 138°29°E
18°43°S, 138°29°E
18°56°S, 139°58’°E
19°03’°S, 140°02’E
19°14°S, 140°21°E
19°1S°S, 140°22°E
17°28°S, 14°11 VE
17°27°S, 140°50°E
17°28°S, 141°1 VE
17°40°S, 141°05’E
L7T°44°S, 139°35°E
18°53°S, 140°28’°E
07 Jan 2002
11 Jan 2001
O9 Jan 2002
12 Jan 2002
13 Oct2012
12 Oct 2012
13 Oct 2012
14 Oct 2012
12 Oct 2012
24 Oct 2012
25 Oct 2012
25 Oct 2012
24 Oct 2012
24 Oct 2012
10 Oct 2012
23 Oct 2012
15 Oct 2012
Ol Nov 2011
12 Oct 2012
13 Oct 2012
14 Oct 2012
13 Oct 2012
13 Oct 2012
14 Oct 2012
11 Oct 2012
12 Oct 2012
Voucher *°* !4
(as juvenile)
Voucher
Obs
Ob S Note 15
Obs-c2 Note 16
Obs
Voucher
Obs
Obs
Fig 7
Obs
Photo Note 17
Photo 2°
Obs
Obs
Obs
Obs
Obs Note 18, Fig 9
Rel
™
Voucher “2 1°
Obs
Rel
Obs Note 19
Obs
Obs
Voucher
3
Ob . Note 20
BEDS PE DS PF OE be PE DS De Pe be Pe be pe Pe bd be bg
Magazine of the Butterfly and Other Invertebrates Club #76 — Page 29
Euploea corinna
16km W by S of Blackall Qld 24°27°S, 145°20°E 03 Oct2012. Obs Ne?!
(along road to Isisford)
Tambo, in hotel rear garden Qld 24°53’S, 146°IS-E =—- 26 Oct 2011 Obs “ete?
Augathella, at Warrego River Qld 25°48’S, 146°3SV°E = 01 Oct 2012 = Obs
ford at 25°47°43” 146°34’48”
Photos Kelvyn Dunn
Fig.1. Y. arctoa male (ventral view) perched at Belyando Crossing; specimen deposited in ANIC, Canberra.
Fig.2. H. metirius male (dorsal view) feeding at Lobelia trigonocaulis (Campanulaceae) at Carnarvon Gorge,
Carnarvon National Park.
Fig.3. H. metirius male (ventral view) feeding at L. trigonocaulis at Carnarvon Gorge.
Fig.4. H. pseudirius aged male (ventral view) feeding at L. trigonocaulis at Carnarvon Gorge
BEDS PERE PS Pe RT be Pe DT be be De be Pe bd Pe
Magazine of the Butterfly and Other Invertebrates Club #76 — Page 30
-
é
Rig. 9 -%
. ™
- + b . a
« * :
Fig.5. H. pseudirius fresh conditioned male (ventral view) perched at Tambo, in hotel rear garden.
Fig.6. C. sempronius at Flinders River crossing, 60km SW of Normanton, feeding at mud (video recorded
in captivity; specimen deposited in ANIC, Canberra).
Fig.7. J. orithya male (dorsal view) basking at Walker Creek, 28km NNE of Normanton.
Fig.8. J. orithya battle scarred male with severed forewing (ventral view) perched at Lawn Hill National Park.
Fig.9. J. orithya aged female (dorsal view) perched at Dismal Creek crossing, 4km ESE of Burke & Wills
Roadhouse.
Fig.10. J. hedonia male (ventral view) roosting at Walker Creek, 28km NNE of Normanton;
specimen deposited in ANIC, Canberra.
TAA ASA A CASATACALASATASASAL ASA CATA
Magazine of the Butterfly and Other Invertebrates Club #76 — Page 31
OMISSION
New Distribution Records for Sulphur and White Butterflies (Lepidoptera:
Pieridae) in inland and outback Australia — Kelvyn L. Dunn, December 2014 issue
of Metamorphosis Australia, #75. The column “Format” in the Table was
inadvertently omitted from the article when transferring it to the magazine which
meant that the numbered biological notes could not be cross-referenced to the
particular records they concerned. The replacement Table is reproduced below.
Table - Forty-nine new locations for species of Pieridae from beyond their
known ranges in Australia
Species/Location State Geocode Date Format
Catopsilia pyranthe
Bladensburg historic homestead, Old 22°30’S, 143°02’E 06 Oct 2012 Obs
at woolshed
1.6km NE by E of Charleville Qld 26°24’S, 146°1IS’°E =. 28 Sep 2012 Obs
30 Sep 2012 voucher \°t*!
Bogan River bridge, at 1.3km NSW ss 331°33’S, 147°1VE — 16 Dec 2013 Obs
NW by W of Nyngan
95km N by W of Condobolin NSW = 32°19’S, 146°S8’E —- 16 Dec 2013 Obs-C2
C. pomona
Muttaburra Qld 22°36’S, 144°33°E =—- 04 Oct 2012 Obs
Aramac, N of Barcaldine Qld 22°58’S, 145°IVE = 04 Oct 2012 Obs
lkm S of Barcaldine Qld 23°34’°8, 145°17E 04 Oct 2012 Obs
Isisford Qld 24°16’S, 144°26’°E =: 03: Oct 2002 Obs
Blackall Qld 24°26’S, 145°28’E =: 02: Oct 2012 Rel
16km W by S of Blackall Qld 24°27°S, 145°20’E 03 Oct2012 Obs"?
(along road to Isisford)
24km NW by rd of Tambo Qld 24°45’S, 146°00’E —s_. 26 Oct 2011 voucher
Tambo Qld 24°53’S, 146°IS’°E =: 02: Oct 2012 Obs
18km N of Augathella Qld 25°39°S, 146°36°E = 01 Oct 2012 Rel
41km NNE of Charleville Qld 26°06’S, 146°25’E = 01 Oct 2012 Obs
1.6km NE by E of Charleville Qld 26°24’S, 146°1IS°E =30 Sep 2012 Obs
l1km S by W of Charleville Qld 26°29’S, 146°13’°E —-. 25 Oct 2011 Obs
12km S by W of Charleville Qld 26°30’S, 146°12’E =. 25 Oct 2011 Obs
25km S by W of Charleville Qld 26°37°S, 146°10E 25 Oct 2011 Obs
(at 4km N of Angellala Creek)
Eurema laeta
Walker Creek, at 28km by Qld 17°28’S, 141°1VE 12 Oct 2012 voucher
road NNE of Normanton 13 Oct 2012 voucher
14 Oct 2012 Rel
Normanton, at drain near Qld 17°41’°S, 141°04’7E—s- 12 Oct 2012 voucher ‘8!
Travers Street 14 Oct 2012 Rel
BEDS PE DS PF DE be PE DS De RE be Pe be pe Pe bd Pe bg
Magazine of the Butterfly and Other Invertebrates Club #76 — Page 32
E. herla
Craggs grave, 27km SSW
by road of Winton
Surprise Creek, at Top
Crossing, at southern boundary
of Bladensburg National Park
E. smilax
27km E of Norseman
13km N of Scaddan (at Truslove
Road junction)
E. hecabe
1.6km NE by E of Charleville
post office (at van park)
Elodina parthia
Bottle Tree Lookout, 58km NE of
Hughenden
18km SE by E of Winton, in cleft
on mesa
24km NW by rd of Tambo
25km SE of Tambo, at highest
point on road
Tara River, at Hebel
El. walkeri
Chillagoe
Skm SE of Chillagoe
Cepora perimale
ll1km N by E of Roma
10km SE by S of Hebel
Deltas argenthona
Walker Creek, at 28km NNE of
Normanton
lkm S of Barcaldine
Barcoo River bridge, Isisford
Barcoo River at 42km ESE of
Blackall
25km NW by rd of Tambo
Tambo
29km NNE of Charleville
1.6km NE by E of Charleville
Wyandra (in hotel rear garden off
Warrego Street)
lkm S of Cunnamulla (at van
park)
Darling River at Bourke, near
Short St (close to Rotary Park)
Qld
Qld
WA
WA
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
NSW
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
Qld
NSW
22°34’S, 142°57°E
22°34’S, 142°58°E
32°05’S, 122°OVE
33°19'S, 121°42°E
26°24°S, 146°1S’E
20°28’S, 144°24°E
20°29°S, 143°11’E
24°45’S, 146°06’E
25°O1’S, 146°26°E
28°58’S, 147°48°E
17°09S, 144°31’E
17°11°S, 144°33’E
26°28’S, 148°48°E
29°02’S, 147°52°E
17°28°S, 141° VE
23°34’S, 145°17°E
24°16°S, 144°27°E
24°35’S, 145°49°E
24°45’S, 146°06’E
24°53’S, 146°15°E
26°11°S, 146°22°E
26°24’S, 146°15°E
27°15°S, 145°59°E
28°0S’S, 145°41°E
30°0S’S, 145°57°E
06 Oct 2012
06 Oct 2012
10 Oct 2008
15 Oct 2008
30 Sep 2012
28 Oct 2011
O05 Oct 2012
26 Oct 2011
O02 Oct 2012
17 Nov 2011
12 Jan 2002
12 Jan 2002
14 Nov 2011
17 Nov 2011
14 Oct 2012
04 Oct 2012
03 Oct 2012
02 Oct 2012
02 Oct 2012
01 Oct 2012
30 Sep 2012
30 Sep 2012
27 Sep 2012
27 Sep 2012
26 Sep 2012
Obs
Photo
Note 3, Fig 2
Voucher
Obs
voucher *°** 4
Voucher ‘°*>
Voucher ‘°°
Fig 3
Fig 4
Voucher
Voucher
voucher
Note 7, Fig 5
Voucher
Photo "2°
Fig 7
Note 8
voucher
voucher
Obs
Obs
Obs
Voucher
Note 9, Fig. 9
Obs
Obs
Voucher
Obs
Photo Fig!
Fig.10
Rel
voucher ‘° 1°
BEDS REDS PF OE Pe PE DS Pe Pe be Pe be pe Pe bd be bg
Magazine of the Butterfly and Other Invertebrates Club #76 — Page 33
D. aganippe
39km E of Isisford Qld 24°16’S, 144°48°E 03 Oct 2002. Obs “°**"!
16km W by S of Blackall Qld 24°27’S, 145°20’E —- 03 Oct 2012 Rel
24km NW by rd of Tambo, at Qld 24°45’S, 146°06’E 02 Oct2012 ~~ voucher \°*””
picnic area
Beacon Hill Lookout, 1.6km Eof WA 32°12’S, 121°49E = 10 Oct 2008 Obs
Norseman 13 Oct 2008 Obs
OK FS FS FS 6 OK OK 2S 2S OK
Brown Stag Beetle (RKhyssonotus nebulosus) in Brisbane —
Hongming Kan
One day 1n late 2008 in Yugarapul park, I accidently stepped on a rotten tree trunk
lying in the bush and snapped it while chasing a beautiful butterfly near the Bulimba
creek. I found a pair of Brown Stag beetles inside the broken tree trunk. That was the
first time I had a close encounter with the amazing beetles and learnt the existence of
such creature. However, after that day and until a few days ago (15 Dec, 2014), I
never had another chance to see them again despite the fact they are common in
Queensland.
I am a big fan of beetles and the
desire to get my hands on the brown
stag beetles again gnawed at me.
With a few weeks’ holidays to spend
on my hobbies at the end of the year,
my hands were becoming itchy and I
felt 1t was the right time to try my
luck again. Before I started, I did
some goolging on the Brown Stag
Beetle. From the information
gleaned, I learnt they actually live
their entire lives inside rotten tree
trunks and it felt like a plausible
explanation why I hadn’t seen them
again in so many years. It never occurred to me before that a rotten log was the
obvious place to search for the beetles although it was the place where I found them
initially. Armed with the knowledge of the beetle’s habits, I knew where to look for
them this time.
The place where I decided to carry out my exploration was the same place where I
first saw the beetles. There are a lot of trees growing along the Bulimba creek with
thick canopies, creating a very humid and shady environment underneath. Inside that
environment the fallen trees are abundant, many of them rotten. I set my sights on a
medium size fallen tree that seemed to be thoroughly rotten because a gentle kick
caused a large chunk of it to break off.
BEDS PE DT PE DE PS Pa Re be Pe be bd Oe be pe bd bd Pe
Magazine of the Butterfly and Other Invertebrates Club #76 — Page 34
7
~ >) LAN
ae x * i@
ee et st a? A. NE AN :
It all looked very promising to me. My first dig using a screwdriver near the root of
the tree broke it into two halves and immediately something black inside caught my
eyes. I was elated and carefully picked them up and placed them in my hands. There
was no doubt they were stag beetles because of the hallmark of the stag beetle, the
mandibles, were on top of their heads but they were not exactly the brown stag beetles
I was looking for because their colours were not right. They were totally black.
Initially I thought I had found a different type of stag beetle! But then something
interesting happened.
While they were in my hands, the colours
on their backs were gradually changing!
At the very beginning, they were indeed
black, but within a few seconds, their
colours changed to brown, revealing the
patterns of the Brown Stag beetle that I
was searching for! In hindsight, I think
when they are wet, their brown sheaths
become black and only when they are dry
do the brown colour and the beautiful
marks show up.
At home, I did more searches on the colour change of the beetle. I haven’t found any
information on the English sites but one Chinese site describes the same colour
change I have witnessed (http://komurohu.pixnet.net/blog/post/38623672-
BEDS PERE PS Pe Pe be PE Re be Pe De be Pe he bd Pe bg
Magazine of the Butterfly and Other Invertebrates Club #76 — Page 35
HEOMICVMAAMET%MIF MAS MES %M8D%ITHEO%IO%MBI%MES MA4%AT%EIMIIN
BEMETHIA84%ES MBO%M8BF%MEO%83%A1L%MEI%MAD%94---rhyssonotus-
nebulosus-%E6%BE%B3
In total, I found 6 brown stag beetles from two rotten tree trunks on that day (15 Dec,
2014). I also found a decomposed body of a Golden Stag beetle inside one of the tree
trunks. It looks like the Brown Stag beetle 1s indeed very common in Queensland but
because of their habit of living inside tree trucks, they are rarely spotted.
Exactly one year ago at the same location, I
found a dead body of the Golden Stag beetle
as shown in the adjacent picture. I have never
been able to find a live one.
I would like to know the information on how
to capture a live golden stag beetle 1f any of
the club members can offer some valuable
insights.
Photos Hongming Kan
TS TK SIS OK OS OK 2 OK ok
A Problem with Identifying Moths - Peter Hendry
Peter Kuttner, from Mt Tamborine, sent me the attached moth images hoping I could
identify them. I concluded, despite the differences, Figs 1 and 2 were the same moth.
I also came to the conclusion that all 3 images were of moths in either the family
Geometridae or Noctuidae. I searched high and low without any success. With both
moths being rather distinctive, I expanded my search into other families despite
believing they belonged to the aforementioned. I called upon a couple of club
members regarding Figs | and 2. They also had no idea. With no success
BEES a OE DT be PED be be Pe bd be Re bd pe Pe bd bd
Magazine of the Butterfly and Other Invertebrates Club #76 — Page 36
forthcoming, I called upon the expertise of Ted Edwards from the Australian National
Insect Collection in Canberra. The answers were quite surprising:
“Fig. 1 and Fig. 2 are a species of Idiodes in the (tribe) Lithinini, (subfamily)
Ennominae, (family) Geometridae. A. J. Turner was aware of this species and had a
manuscript name for it but died before the name was published. It is reasonably
common in the S. Qld and N. NSW rainforests.
Fig. 3 1s more of a problem. I could not match it with anything in the ANIC and it
may be a new species but I could not be sure. It 1s closest to Planolocha obliquata,
another Lithinini.”
So if you are having problems
— identifying a moth, in spite of how
distinctive it might be, the reason may
be it is just unnamed.
A.J. Turner (1861-1947) was a
Paediatrician and Entomologist and is
responsible for naming more than
3,500 species of Australian
_ Lepidoptera, more than any other
author.
Many thanks to Peter Kuttner for his inquiry and special thanks to Ted Edwards for
his rapid response to my query. Photos Peter Kuttner
ok ok 2k ok ok ok ok ok ok ok
Unusual butterfly life history aberrations — Wesley Jenkinson
Having a passion for observing life histories of Australia’s butterflies since an early
age, including moths as well in the last few years, it seems there is always something
new to discover. Whether it is a new larval host plant for one of our butterflies (which
one would think most would have already been discovered ) or countless unknown
moth larval hosts/host plants (most of which are still largely unknown) there will
always be a few oddities. Below are four previously unpublished examples from the
past few years.
BEES Pe DE PT be PED be Pe Pe bd be Re be pe Pe bd bd
Magazine of the Butterfly and Other Invertebrates Club #76 — Page 37
1/ During a trip to northern New South Wales with John Moss during February 2012,
at a roadside stop near the Gyra-Ebor / Rockvale Road intersection, a male melanistic
form of the Spotted Brown (Heteronympha paradelpha) was captured. The adults of
both sexes were very common at this location.
Male melanistic form Male normal form
2/In March 2013 while about to enjoy chewing on a nice fresh sweet corn cob straight
from the vegetable garden, I noticed a tunnelling larva. Thinking it was a larva of the
commercial pest Corn Earworm (Helicoverpa armigera) moth, it was about to be
squashed. On a closer inspection it was an unexpected larva of the attractive Bright
Cornelian butterfly (Deudorix diovis). The larva and corn were kept 1n a container for
observation.
After four days the larva started to pupate and formed a perfect pupa. However the
adult failed to emerge. I have a Tulipwood tree (Harpullia pendula), known hostplant
for this butterfly, which is growing about 4-5 metres from where the corn was
erowing. Most likely the larva was dislodged from an Harpullia seed capsule and
crawled over onto the corn and continued feeding within the cob in an effort to
Survive.
Images - View showing part of tunnel and dorsal rear view of larva hard anal plate and ejected
‘yellow’ frass in container
BEDS PERT PS Pe Re Pe Pe Re be Pe De be Pe be bd Pe be
Magazine of the Butterfly and Other Invertebrates Club #76 — Page 38
3/ During late 2012, a lycaenid specimen was given to me for setting by our club
president Ross Kendall. Ross reported that the larva had been located and raised to an
adult on a cultivated citrus tree.
The specimen was identified as a very small female Cycad Blue (Theclinesthes
onycha), and no doubt growth retarded by an unsuitable host plant. On several
occasions I have observed females of this species ovipositing on the buds of Rose
plants (Rosa spp.) and once on Rattle Pod plants (Crotalaria spp.), in which the
resultant larvae didn’t accept either plants and died.
Images- (Photographed together) Female Theclinesthes onycha with wingspans 17mm and 28mm
4/In April 2013 several first and second instar larvae of the Tailed Emperor (Polyura
sempronius) were located feeding on the same Crotalaria growing in my garden. The
larvae were ‘sleeved’ on the plants with netting bags. They all failed to survive on
these plants although they successfully utilise many other legumes in at least four
plant families; eg Moss (2010) lists 40 species for this region.
Over the years there have been a number of other abnormalities of individual butterfly
specimens that others 1n our group have identified or collected. These include a
gynandromorph Orchard Swallowtail, yellow painted Glasswing, albino Lemon
Migrant, hybrid Yellow/Orange Migrants and a melanistic Large Grass-Yellow with
all yellow markings replaced by light brown!
Occasionally ovipositing females seem to ‘get it wrong’ when it comes to egg laying
on their host plants. This is one aspect that can make field observations very
interesting, as one does not know just where and when the next discovery will be!
Photos Wesley Jenkinson
Reference:
Moss, J. T., 2010. Butterfly Host Plants of South-east Queensland and northern New South
3" ed. BOIC.
BEDS PE DS PE DE PS Pa Re be Pe De be Oe be Pe be bd Pd
Magazine of the Butterfly and Other Invertebrates Club #76 — Page 39
LETTER
Via email from Garry Sankowsky, North Queensland — 1.2.2015
Hi Daphne,
The dry 1s certainly over here with storms every other day and the butterflies are
really on the go. We had a migration of Lemon Migrants here at the same time as
south Qld so there may have been a massive overwintering colony somewhere. They
were all form crocale (Catopsilia pomona crocale) so they did not hatch after the
Dec/Jan rains or they would have been C. pomona. Even though the Brigalow Scrub
in central Qld has been completely exterminated large numbers of Cassia brewsteri
have survived due to their persistent suckering ability and they can still produce huge
numbers of migrants. Nothing like in the 60's but still big numbers.
Cheers Garry
ARTICLES FROM PAST ISSUES
From Issue #47 December 2007
The Caper White Migration — Peter Hendry
The Caper White butterfly (Belenois java) has made another impressive migration this
year. The migration has been noted in our newsletter in past reports including No.12,
March 1999, p.15 wherein John Moss reported on “Fellow- travellers in a Caper White
Migration” in October 1998. In No.31, December 2003, p.32, David St Henry in his
report (from North Rockhampton) on the Lakes Creek State School butterfly habitat
regeneration project, recorded seeing a migration in 2003 and in No.43, December
2006, p.22, Mary Hackett from her herb farm at Middle Dural NSW wrote on the 2005
migration : “Their mass migration overwhelmed me in the garden as I stood with arms
extended, exchanging salutations as they dipped and brushed my hair and fingertips in
passing.”
So let’s take a closer look at the butterfly and its migration. The Caper White is a
medium sized butterfly with a wingspan of 55mm. There are two subspecies of Caper
White in Australia, Belenois java teutonia and Belenois java peristhene. On the
mainland B. 7. peristhene has only been
recorded on the east coast at Percy Isles
northeast of Shoalwater Bay QLD and near
Sydney NSW. B. j. teutonia occurs in two
colour forms, pale and dark, the dark form
being most notable 1n the females. While the
pale form of the female 1s similar to the male,
the dark form has a much broader black
suffusion around the edge of the wings. The
larvae feed on species in the plant family
Capparaceae, mostly in the genus Capparis,
A mating pair
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but also use the Warrior Bush (Apophyllum anomalum) which 1s widespread 1n semi-
arid areas of NSW and southwest QLD. The pale yellow eggs, which later turn orange,
are 1.4mm high x .8mm and are laid in clusters. One female was reported laying 114
eggs in 30 minutes! The larvae reach 32mm in length and are olive green to chocolate
brown in colour, with numerous raised yellow spots. The pupa is up to 25mm long,
usually mottled white with black patches, but sometimes pinkish white or almost wholly
white or wholly black. No one really understands the reason for the migration. One
theory is that the larvae build up in such large numbers that they devoid the area of
available host plant and the adults migrate to find more. However in many cases they fly
into areas where no host plants exist or fly straight out to sea, to a certain death. It is
reported that the migration takes place every year and in some years goes unnoticed due
to the lack of numbers. I cannot imagine the host plants being completely stripped in
those years, unless due to lack of intervening good rain, they have not recovered from
previous years. The direction of the migration varies not only depending on where it 1s
observed, but even varies during the migration. *Braby, quotes several sources which
give the following directions: In southeast QLD, southeasterly migrations; inland
southern NSW, southerly; ACT, northeasterly; Sydney, both northerly and southerly;
central VIC, westerly; northwest VIC, southeasterly. *“R.Grund, 1n a web article on
South Australian butterflies, stated “the migrations proceeded southerly to the lower
southeast region of South Australia and to southwest Victoria, then turned west to the
Fleurieu Peninsula, Kangaroo Island and Yorke Peninsula, and then made a northerly
turn before disappearing back north, presumably from where they started”. So there
remains much to learn.
As the migrations 1n Queensland take place during October and November, and as |
take holidays during that period, I am privy to some marvelous sights during large
migrations. It is hard to contemplate the number of individuals involved. In 2005 I
drove from Sheldon (near Brisbane) to my bush block west of Bundaberg and saw
Caper Whites the full length of the journey. They were so thick just south and north of
Maryborough I could not drive without hitting them. That year I stood in my mother’s
garden at Manly (Brisbane) and counted 16 crossing a 20metre line in one minute. This
year, on the 27" of October, I was on a 1000
acre block near Deepwater, south of
Tenterfield, 1n NSW and saw hundreds taking
nectar from two species of Tea Tree
(Leptospermum) which were in full flower,
but it was a small patch of Callistemon
pungens that really attracted their attention.
Whether it was the flower colour (mauve - as
opposed to the white leptospermums) or the
fact that the bottlebrush had recently opened
(with a possible higher nectar content) it was
the preferred species. Adult feeding on Callistemon pungens
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Magazine of the Butterfly and Other Invertebrates Club #76 — Page 41
I later returned to the bush block west of Bundaburg (during overcast and showery
conditions) where I found larvae and eggs on a caper species (Capparis canescens) 1n
the open forest area. Down by the river in the vine scrub where Capparis arborea and
C’. sarmentosa grow, John Moss and I observed a mating frenzy. All of the Caper
Whites were pairing up, except one particular female, which when males approached
raised her abdomen, as if willing to accept a mate, but none obliged! We observed this
behavior for some time, and no mating occurred. In researching for this article I read
that the females do this to let the males know they are already fertile; my observations
seem to bear this out. The butterflies here showed no obvious signs of migrating, but
this may have been due to the overcast conditions. The most observed species flying
were Caper Whites and Large Grass-yellows. Many of the pupae found were attached
to other nearby plants and some appeared to be parasitised, but after reading that the
pupae can be coloured black I am not so sure.
When migrating the female will stop and lay on any host plants they find, dispensing
large numbers of eggs at a time. During
one migration the late Dr G. A.
Waterhouse estimated a total of
250,000 eggs were laid on a large tree
caper in his garden. Eggs have been
reported to be laid on some non host
plants, including cultivated orange,
Zieria sp. and Correa baeuerlenii
(Rutaceae), as well as Banksia ornata
and B. serrata (Proteaceae). As expected the resulting larvae do not survive and in many
cases the eggs are infertile. During these times many home gardeners with cultivated
Capparis species will experience defoliation of their plants. In my Sheldon garden, my
Capparis arborea 1s planted in heavy shade and generally seems to be left alone for this
reason. However this year, for the first time, I found 101 eggs on one leaf, possibly from
one female.
Eggs on Capparis canescens
Apart from all the media reports, some of our members have reported the following.
Richard Zietek said all of his Capparis species have been stripped clean this year.
Daphne Bowden tells the story that while attending the local Spring Parade on the
waterfront at Manly, when the pipe band struck up to start the parade, as 1f on cue, a
large cloud of resting Caper Whites rose from the wall (or maybe the sand) of the
Esplanade to continue on their merry way. Lois
Hughes said she was dragged kicking and
™ screaming by husband John up the slopes of Mt
- Cotton to two isolated C. arborea trees
completely covered in butterflies and still
containing many larvae and pupae. (I may have
embellished “the kicking and screaming” bit,
but she was in a long dress and dress shoes!)
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Magazine of the Butterfly and Other Invertebrates Club #76 — Page 42
Pupa on anon host plant Acalypha sp.
While we may not fully understand the Caper White migrations, they are great
ambassadors for the insect world as they do stir up the media and have the general
public talking on a subject many would not normally bother with.
Photos by Peter Hendry
References: * Michael F Braby, 2000 : Butterflies of Australia : their
Identification, Biology and Distribution. CSIRO
** South Australian Butterflies Data Sheet R. Grund
http://users.sa.chariot.net.au/~erg/java_ ds.htm
OTHER GROUPS’ ACTIVITIES
Redlands Good Gardening Expo - Saturday 11 April 2015 9am to 3pm
Held at: Redlands IndigiScapes Centre, 17 Runnymede Rd, Capalaba
Free Entry! Find out about growing your own organic food at home. Tastier, healthier, the way
it was meant to be eaten. Learn about native gardening and how you can use natives to create
habitats. Composting, worm farming, mulching and how to recycle your green waste. Buy
plants and seeds and get some great new ideas for your garden. Get the help you need with
advice from the experts. Workshops & demonstrations, arts & crafts, music & food!
Indigi Day Out Saturday 6" June 10am to 4pm. Discover the wonders of IndigiScapes at
this fun-filled event! There will be wildlife displays, mini workshops, music, arts and craft, kids
activities, and food to enjoy.
BUTTERFLY AND OTHER INVERTEBRATES CLUB PROGRAMME
AGM - 18" April, 2015, at Redlands Indigiscapes Centre, Capalaba —
See enclosed flyer. The meeting will be followed by a guided walk through
the gardens and bush area of IndigiScapes.
Planning and General 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. A walk
around the lake will follow the meeting.
When: Saturday May 9", 2015 from 10 am
Where: Marie-Louise Johnson’s place at Forest Lake - address provided on RSVP
Who: All members are welcome.
RSVP: Marie-Louise on 0422 970 184 or email nabid@aapt.net.au
Indigi Day Out Saturday 6" June, 2015 - 10am to 4pm.
See details in Other Groups’ Activities — We will have a display at this event.
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Magazine of the Butterfly and Other Invertebrates Club #76 — Page 43
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 is a platform for people, both
amateur and professional, to express their views and observations about invertebrates. These
are not necessarily those of the BOIC. The manuscripts are submitted for comment to
entomologists or people working in the area of the topic being discussed. 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 is done with the efforts of:
e Those members who have sent in letters and articles
Lois Hughes who provided the cover painting
Daphne Bowden who works on layout, production and distribution
John Moss, Dr Anne Dollin and Martyn Robinson for
scientific referencing and proof reading of various
articles in this issue of the magazine oan
e Printing of this publication is proudly supported by TT
Brisbane City Council sete EELS,
We would like to thank all these people for their contribution. Pjedicated to a hetter 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 $30.00 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 number and surname e.g. 234 Roberts.
Butterfly and Other Invertebrates Club Inc.
PO Box 2113
RUNCORN Q. 4113
Next event - AGM — 18" April, 2015, at Redlands Indigiscapes Centre, Capalaba
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Magazine of the Butterfly and Other Invertebrates Club #76 — Page 44