Compiler and date details
15 June 2009 - Updated by ABRS following Brock & Hasenpusch (2007, 2009).
30 June 1997 - John Balderson, D.C.F. Rentz & A.M.E. Roach, CSIRO Entomology, Canberra, Australian Capital Territory, Australia
The Phasmida, commonly known as stick and leaf insects, are large (35–240 mm in length), terrestrial, often thamnophilus or tree-dwelling insects attaining the greatest abundance in tropical climes. In terms of length, they are among the world's largest insects. Most species show remarkable resemblance to plant parts, such as twigs, leaves and stems. Several species have been used widely in behavioural and physiological studies while others have been of considerable use in cytological investigations.
Kevan (1982) estimated that 2500 species of Phasmatodea were described worldwide; Brock and Hasenpusch (2009) give a figure of 'about 3000' species worldwide. Key (1991) estimated that the Australian fauna would probably reach about 150 species when all species are described. Brock & Hasenpusch (2007, 2009) list 104 described species for Australia.
Genetic variation in anatomical characters occurs in many, if not most, species. This has led to many errors in taxonomy. Lobes, 'horns', spines and differences in rugosity can be highly variable or absent among individuals of the same population. Green and non-green morphs also often occur in the same population. This, coupled with geographic variation, size and wing variation, and the fact that males are much smaller and quite different in appearance from females, has confounded the taxonomic literature.
Stick insects have had a taxonomic history somewhat similar to that of cockroaches and mantids. They were considered as a family of Orthoptera in the early days but are now generally recognised as a separate order. However, the names used for the order often vary with the author. Cheleutoptera, Phasmida, Phasmodea, Phasmatodea, Phasmatoptera and Phasmoptera have all been used to designate the order. The classification used in the Catalogue (Balderson et al. 1998) follows that of Key (1991) which was developed from that of Günther (1953). The classification of Bradley & Galil (1977) escalated in rank many taxa without providing any reasons. Kevan (1977, 1982) further escalated ranks without much explanation. Three families are now recognised among Australian species: Diapheromeridae with two subfamilies, Phylliidae with one and Phasmidae with six (Brock and Hasenpusch (2009).
Bedford (1978) provided a comprehensive, world review of the biology and ecology of stick insects. Kevan (1982) provided a similar review at the taxonomic level. His 'escalated' view of the higher taxonomic levels is not followed here. Regular notes on the behaviour and ecology of stick insects, including Australian species, can be found in the Newsletter of the Phasmid Study Group (ISNN 0268–3806) and their journal, Phasmid Studies (ISSN 0966–0011).
Brock and Hasenpusch (2009) give a very useful comprehensive review of stick and leaf insect biology and history of collecting of Australian stick and leaf insects. They also detail methods for collection, rearing and preserving stick insects and give a summary of information on each of the described species.
Phase differences (often called kentromorphism in Australia) have been reported by Key (1957) in three Australian stick insects. These are Podacanthus wilkinsoni Macleay, Didymuria violescens (Leach) and Ctenomorphodes tessulatus (Gray), all of which can reach high population numbers. Low density nymphs are uniformly coloured—usually green, while those prone to high density populations are aposematically coloured and patterned. Morphometric phase differences are analogous to those of locusts. There is no correlation between density and activity, and stick insects show no obvious gregariousness.
One species, the Lord Howe Island stick insect, Drycocelus australis (Montrouzier), was believed to be extinct (Gurney 1947; Smithers 1969). It was endemic to Lord Howe Island where it lived on the trunks and in cavities of banyans. It is thought to have been exterminated after rats were introduced to the island in the early part of the century. It was found on the offshore Ball's Pyramid in 2001, and is being reared for release back on the Island.
Most stick insect species seem to be nocturnal and, with a few exceptions, rare in nature. Most species are found in foliage upon which they feed but a few are wholly terrestrial. They are entirely plant feeders and are unusual in their ability to develop on a wide variety of unrelated plant species. They exhibit cryptic postures and perform rhythmical swaying when disturbed. A few species can produce sound when disturbed by rubbing the hind wings against tubercles on the legs. There is no indication that they can hear any of the sounds they produce. When disturbed, some species drop to the ground in a state of catelepsy that may last for hours. Other defensive responses in Australian species have been described by Bedford & Chinnick (1966). Australian Megacrania species squirt a milky substance smelling of peppermint, probably actinidine for M. alpheus Westwood (Chow & Lin 1986), at intruders when disturbed.
Morphologically, stick insects are very distinctive. They are generally prognathous with the head ovoid to rectangular, often with horns or protuberances. The antennae are short to long, ranging from 8 to more than 110 segments. Eyes are small and inconspicuous; ocelli are present only in some winged species. The prothorax is longer than the other thoracic segments (in contrast to the stick katydids, Tettigoniidae: Phasmodinae, in which the metathorax is the expanded thoracic segment). All three pairs of legs are gressorial and are long and slender. Tarsi of all Australian species are 2–5-segmented. Many species have the capability of being able to regenerate lost appendages if they are lost at an early stage of development. In those limbs, the tarsi are 4-segmented. Terminal claws bear an arolium. Both sexes of most Australian Phasmatodea are apterous, however, males of some species are fully winged, the females wingless or semi alate. The forewings are toughened tegmina, which are often small, rounded and dome-like and cover the base of the hind wings at rest and slightly overlap. The forewings typically have a knob-like structure dorsally in the proximal portion that accommodates a prominent sclerite on the base of the hind wing when folded. The hind wings are large, broad, with a large membranous anal area, folded fan-like at rest. Venation is very uniform; costa absent in forewing, weak and positioned on the anterior margin of hind wing; subcosta unbranched; radius unbranched in forewing, branching in hind wing forming R1 and radial sector; media bifurcate in forewing, in hind wing only basally and occasionally trifurcate.
Abdomen cylindrical or dorso-ventrally compressed, with or without spines or outgrowths; abdomen 11-segmented with the first tergite called the median segment, connected to metanotum (Australian species); tenth tergite well developed, emarginate posteriorly in males with ventro-caudal angles produced, clasping, often with small tufts of spines, lateral walls of this tergite curving ventrally or meeting the mid-ventral line anteriorly; eleventh tergite constituting the supra-anal plate, often concealed under T-10 in males, more elongate, often articulated in females. Sternite 10 well developed, fused posteriorly to the paraprocts. Cerci unsegmented, long or short, often concealed beneath the tenth tergite, often modified as claspers in males. In males the ninth sternite constitutes the subgenital plate which lacks styles but is modified distally into a cup-like lobe, often termed the poculum. The tenth sternite in males of some groups is provided with a backwardly projecting prong-like process, the vomer, which is used in copulation. The genitalia are concealed by the subgenital plate and constitute a group of symmetrical, membranous or lightly sclerotised lobes. Females are different in the structure of the posterior abdominal segments. The eighth sternite consists of a scoop-like or keeled structure called the operculum, the posterior margin of which may project beyond the abdomen and frequently bears an egg. The ovipositor is very short and consists of three pairs of valves, and is wholly concealed by the operculum.
The chromosome complements of Australian Phasmatodea range in number from 26 to 69, the larger numbers occurring in parthenogenetic species. Males usually are XO but XY species are known. Intricate studies illustrating chromosome races have been done by Craddock (1972) and varying chromosome numbers in parthenogenetic females have been demonsrated in the genus Sipyloidea by John et al. (1987).
Eggs of stick insects are of special interest because of their resemblance to seeds. The chorion is hard and may be wrinkled or smooth and patterned. The anterior pole bears an operculum and it in turn may bear a median prominence, the capitulum. On the dorsal surface there is usually a well-defined micropylar plate that resembles the scar-like hilum of seeds. The microstructure of stick insect eggs provides many reliable taxonomic characters. The eggs of Sipyloidea nelida Rentz are unique in that they are enclosed in two supernumerary membranes. Shortly after deposition, the membranes rupture and a system of tubules in the operculum everts forming a cluster of stellate hairs resembling the head of a dandelion. These have been shown to be connected to the inside of the egg and may transport moisture.
Stick insect nymphs may or may not resemble adults. They are often mimetic, resembling ants. Males undergo fewer moults than females and the exuviae are usually eaten. The number of antennal segments increases progressively.
Originally this section of the Australian Faunal Directory was derived from the Zoological Catalogue of Australia database, from which the published Catalogue (Balderston et al. (1998) was prepared at CSIRO Entomology, Canberra and the Division's resources and facilities were made available to the authors.
The authors were greatly aided by the kindness of several individuals. The Phasmid Study Group is an international organisation of amateurs and professionals dedicated to the understanding of the systematics, biology and ecology of stick-insects. Several members of that organisation provided invaluable help: Mr Paul Brock contributed photographs and notes on the type specimens of a number of Australian species he had studied in the BMNH and various museums in Europe. He also helped to locate important literature which was unknown to the authors prior to the study. Mr Phil Bragg, also a member of the above-mentioned organisation, provided the authors with a copy of his Phasmatid Database. This document will eventually list all of the stick-insect taxa and their dates of publication, references, type localities and location of types. The authors acknowledged the comprehensive catalogue and reference list of Australian species prepared by Vickery (1983) and thanked Mr Jon Prance of the CSIRO Black Mountain Library for assistance and time spent with the literature search.
The illustrations used in the family introductions in the published Catalogue are from Key (1991). They were reproduced with permission from CSIRO Entomology and the Melbourne University Press.
Funding was made available for the original checklisting project by the Australian Biological Resources Study.
The original information on the Australian Faunal Directory site for the Phasmida was derived from the Zoological Catalogue of Australia database compiled on the Platypus software program. It has now been upgraded and updated following Brock and Hasenpusch (2007, 2009).
Distribution data in the Directory is by political and geographic region descriptors (IBRA) and serves as a guide to the distribution of a taxon. For details of a taxon's distribution, the reader should consult the cited references (if any) at genus and species levels.
Australia is defined as including Lord Howe Is., Norfolk Is., Cocos (Keeling) Ils, Christmas Is., Ashmore and Cartier Ils, Macquarie Is., Australian Antarctic Territory, Heard and McDonald Ils, and the waters associated with these land areas of Australian political responsibility. Political areas include the adjacent waters.
Terrestrial geographical terms are based on the drainage systems of continental Australia, while marine terms are self explanatory except as follows: the boundary between the coastal and oceanic zones is the 200 m contour; the Arafura Sea extends from Cape York to 124°E; and the boundary between the Tasman and Coral Seas is considered to be the latitude of Fraser Island, also regarded as the southern terminus of the Great Barrier Reef.
Distribution records, if any, outside of these areas are listed as extralimital. The distribution descriptors for each species are collated to genus level. Users are advised that extralimital distribution for some taxa may not be complete.
Balderson, J., Rentz, D.C.F. & Roach, A.M.E. 1998. Phasmatodea. pp. 347-376 in Houston, W.W.K. & Wells, A. (eds). Zoological Catalogue of Australia. Archaeognatha, Zygentoma, Blattodea, Isoptera, Mantodea, Dermaptera, Phasmatodea, Embioptera, Zoraptera. Melbourne : CSIRO Publishing, Australia Vol. 23 xiii 464 pp.
Bedford, G.O. 1978. Biology and ecology of the Phasmatodea. Annual Review of Entomology 23: 125-149
Bedford, G.O. & Chinnick, L.J. 1966. Conspicuous displays in two species of Australian stick insects. Animal Behaviour 14: 518-521
Bradley, J.C. & Galil, B.S. 1977. The taxonomic arrangement of the Phasmatodea with keys to the subfamilies and tribes. Proceedings of the Entomological Society of Washington 79: 176-208
Brock, P.D. & Hasenpusch, J. 2007. Studies on the Australian stick insects (Phasmida), including a checklist of species and bibliography. Zootaxa 1570: 1-81
Brock, P.D. & Hasenpusch, J.W. 2009. The Complete Field Guide to Stick and Leaf Insects of Australia. Collingwoord, Victoria : CSIRO Publishing 204 pp.
Chow, Y.S. & Lin, Y.M. 1986. Actinidine, a defensive secretion of the stick insect, Megacrania alpheus Westwood (Orthoptera: Phasmatidae). Journal of Entomological Science 21: 97-101
Craddock, E. 1972. Chromosomal diversity in the Australian Phasmatodea. Australian Journal of Zoology 20: 445-462
Günther, K. 1953. Über die taxonomische Gliederung und die geographische Verbreitung der Insektenordnung de Phasmatodea. Beiträge zur Entomologie (Berlin) 3(5): 541-563
Gurney, A.B. 1947. Notes on some remarkable Australasian walkingsticks, including a synopsis of the genus Extatosoma (Orthoptera: Phasmatidae). Annals of the Entomological Society of America 40(3): 373-396
John, B., Rentz, D.C.F. & Contreras, N. 1987. Extensive chromosome variation in the stick insect genus Sipyloidea Brunner von Wattenwyl (Phylliidae: Necrosciinae) within Australia, and descriptions of three new species. Invertebrate Taxonomy 1: 603-630
Kevan, D.E.McE. 1982. Phasmatoptera. pp. 379-383 in Parker, S.P. (ed.). Synopsis and Classification of Living Organisms. New York : McGraw Hill Vol. 2.
Kevan, D.K.McE. (ed.) 1977. The higher classification of the orthopteroid insects. Lyman Entomol. Mus. Res. Lab. Memoir No. 4. 26 pp.
Key, K.H.L. 1957. Kentromorphic phases in three species of Phasmatodea. Australian Journal of Zoology 5: 247-284
Key, K.H.L. 1991. Phasmatodea (Stick-insects). pp. 394-404 in CSIRO (ed.). The Insects of Australia. A textbook for students and research workers. Melbourne : Melbourne University Press Vol. 1 xiii 542 pp.
Smithers, C.N. 1969. On some remains of the Lord Howe Island phasmid (Dryococelus australis Montrouzier)) (Phasmida) from Ball's pyramid. Entomologist's Monthly Magazine 105: 252
Vickery, V.R. 1983. Catalogue of Australian stick insects (Phasmida, Phasmatodea, Phasmatoptera, or Cheleutoptera). CSIRO Aust. Div. Entomol. Tech. Pap. No. 20. 15 pp.
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