The Hepialidae are a family of insects in the lepidopteran order. Moths of this family are often referred to as swift moths or ghost moths.
Taxonomy and systematics
The Hepialidae constitute by far the most diverse group of the infraorder Exoporia. The 82 genera contain at least 700 currently recognised species of these moths worldwide. The genera Fraus (endemic to Australia), Gazoryctra (Holarctic), Afrotheora (Southern African), and Antihepialus (African) are considered to be among the most basal, containing four genera and about 51 species with a mostly relictual southern Gondwanan distribution and are currently separated from the Hepialidae sensu stricto which might form a natural, derived group. The most diverse genera are Oxycanus with 78 species, Endoclita with 78 species, and Thitarodes with 80 species following a comprehensive catalogue of Exoporia. Like other Exoporia, sperm is transferred to the egg via an external channel between the ostium and the ovipore. In contrast, other non-Ditrysian moths possess a common cloaca.
Distribution
thumb|left|[[Abantiades latipennis, Tasmania, Australia]]
Hepialidae are distributed on ancient landmasses worldwide except Antarctica but with the surprising exceptions of Madagascar, the Caribbean islands and in Africa, tropical West Africa. It remains to be borne out if these absences are real as Aenetus cohici was not long ago discovered in New Caledonia. In the Oriental and Neotropical regions hepialids have diversified in rainforest environments, but this not apparently the case in the Afrotropics. which emit a pheromone from scales on the metathoracic tibiae. In such cases of sex role reversal, there may be visual cues also: males of the European ghost swift are possibly the most frequently noticed species, being white, ghostly and conspicuous when forming a lek at dusk. Sometimes they hover singly as if suspended from a thread or flying in a figure of eight motion.
Biology
The female does not lay its eggs in a specific location but scatters ("broadcasts") them while in flight, sometimes in huge numbers (29,000 were recorded from a single female Trictena, which is presumably a world record for the Lepidoptera). The maggot-like larvae feed in a variety of ways. Probably all Exoporia have concealed larvae, making silken tunnels in all manner of substrates. Some species feed on leaf litter, fungi, mosses, decaying vegetation, ferns, gymnosperms and a wide span of monocot and dicot plants. There is very little evidence of hostplant specialisation; whilst the South African species Leto venus is restricted to the tree Virgilia capensis this may be a case of "ecological monophagy". The pupae can then climb up and down to adjust to changes in temperature and flooding. Before the adult moth emerges, the pupa protrudes half way out at the ground surface. The pupa has rows of dorsal spines on the abdominal segments as in other lower members of the Heteroneura. The witchetty grub (which are sometimes hepialid larvae) is a popular food source especially among aboriginal Australians. In Central America and South America, hepialid larvae are also eaten. However, some species of Wiseana, Oncopera, Oxycanus, Fraus and Dalaca are considered pests of pastures in Australia, New Zealand, and South America.
Faunas
Fauna of Europe
Source and identification
- Gazoryctra fuscoargenteus <small>O. Bang-Haas 1927</small> – Northern Scandinavia
- Gazoryctra ganna <small>(Hübner 1808)</small> – Alps, northern Scandinavia, northern Russia
- Hepialus humuli <small>Linnaeus 1758</small> (ghost moth) – Europe
- Korscheltellus lupulina <small>Linnaeus 1758</small> (common swift) – Europe
- Pharmacis aemiliana <small>Costantini 1911</small> – Italy
- Pharmacis anselminae <small>Teobaldelli 1977</small> – Italy
- Pharmacis bertrandi <small>Le Cerf 1936</small> – France
- Pharmacis carna <small>Denis & Schiffermüller 1775</small> – Central and Eastern Europe
- Pharmacis castillana <small>Oberthür 1883</small> – Spain
- Pharmacis claudiae <small>Kristal & Hirneisen 1994</small> – Italy
- Pharmacis fusconebulosa <small>De Geer 1778</small> (map-winged swift) – Europe
- Pharmacis pyrenaicus <small>Donzel 1838</small> – Pyrenees
- Phymatopus hecta <small>Linnaeus 1758</small> (gold swift) – Central and northern Europe
- Triodia adriaticus <small>Osthelder 1931</small> – Croatia, North Macedonia, Greece, Crete
- Triodia amasinus <small>Herrich-Schäffer 1851</small> – Balkans
- Triodia sylvina <small>Linnaeus 1761</small> (orange swift) – Europe
Generic checklist
- Fraus Walker, 1856
- =Hectomanes Meyrick, 1980
- =Praus; Pagenstacher, 1909
- Gazoryctra Hübner, [1820]
- =Garzorycta; Hübner, [1826]
- =Gazoryctes; Kirby, 1892
- Afrotheora Nielsen and Scoble, 1986
- Antihepialus Janse, 1942
- =Ptycholoma; Felder, 1874
- Bipectilis Chus and Wang, 1985
- Palpifer Hampson, [1893]
- =Palpiphorus; Quail, 1900
- =Palpiphora; Pagenstacher, 1909
- Eudalaca Viette, 1950
- =Eudalacina Paclt, 1953
- Gorgopis Hübner, [1820]
- =Gorcopis; Walker, 1856
- Metahepialus Janse, 1942
- Dalaca Walker, 1856
- =Huapina Bryk, 1945
- =Maculella Viette, 1950
- =Toenga Tindale, 1954
- Callipielus Butler, 1882
- =Stachyocera Ureta, 1957
- Blanchardinella Nielsen, Robinson & Wagner, 2000
- =Blanchardina Viette, 1950, nec Labbe, 1899
- Calada Nielsen and Robinson, 1983
- Puermytrans Viette, 1951
- Parapielus Viette, 1949
- =Lossbergiana Viette, 1951
- Andeabatis Nielsen and Robinson, 1983
- Druceiella Viette, 1949
- Trichophassus Le Cerf, 1919
- Phassus Walker, 1856
- Schausiana Viette, 1950
- Aplatissa Viette, 1953
- Pfitzneriana Viette, 1952
- Cibyra Walker, 1856
- Cibyra (Pseudodalaca Viette, 1950)
- Cibyra (Gymelloxes Viette, 1952)
- Cibyra (Alloaepytus Viette, 1951)
- Cibyra (Aeptus) Herrich-Schäffer, [1858]
- Cibyra (Thiastyx Viette, 1951)
- Cibyra (Schaefferiana Viette, 1950)
- Cibyra (Paragorgopis Viette, 1952)
- Cibyra (Hepialyxodes Viette, 1951)
- Cibyra (Xytrops Viette, 1951)
- Cibyra (Cibyra Walker, 1856)
- Cibyra (Lamelliformia Viette, 1952)
- Cibyra (Tricladia Felder, 1874)
- =Pseudophassus Pfitzner, 1914
- =Parana Viette, 1950
- Cibyra (Pseudophilaenia Viette, 1951)
- Cibyra (Philoenia Kirby, 1892)
- =Philaenia auctt.
- Cibyra (Yleuxas Viette, 1951)
- Phialuse Viette, 1961
- Roseala Viette, 1950
- Dalaca auctt., nec Walker, 1856
- Pfitzneriella Viette, 1951
- Aoraia Dumbleton, 1966
- =Trioxycanus Dumbleton, 1966
- Triodia
- =Alphus Wallengren, 1869, nec Dejean, 1833
- Korscheltellus Börner, 1920
- Pharmacis Hübner, [1820]
- Thitarodes Viette, 1968
- =Forkalus Chu and Wang, 1985
- Phymatopus Wallengren, 1869
- =Hepiolopsis Börner, 1920
- =Phimatopus; auctt.
- Phymatopus auctt. nec Wallengren, 1869
- Hepialus Fabricius, 1775
- =Hepiolus Illiger, 1801
- =Epialus Agassiz, 1847
- =Epiolus Agassiz, 1847
- =Tephus Wallengren, 1869
- =Trepialus; Latreille, [1805]
- Zenophassus Tindale, 1941
- Sthenopis auctt. nec Packard, [1865]
- Endoclita; Felder, 1874
- =Endoclyta, Felder, 1875
- =Hypophassus, Le Cerf, 1919
- =Nevina, Tindale, 1941
- =Sahyadrassus, Tindale, 1941
- =Procharagia, Viette, 1949
- Neohepialiscus Viette, 1948
- Elhamma Walker, 1856
- =Perissectis Meyrick, 1890
- =Pericentris; Pagenstacher, 1909
- =Zauxieus Viette, 1952
- =Theaxieus Viette, 1952
- Jeana Tindale, 1935
- Cladoxycanus Dumbleton, 1966
- Wiseana Viette, 1961
- =Porina Walker, 1956, nec d'Orbigny, 1852
- =Gorina; Quail, 1899
- =Goryna; Quail, 1899
- =Philpottia Viette, 1950, nec Broun, 1915
- Heloxycanus Dugdale, 1994
- Dumbletonius; auctt
- =Trioxycanus Dumbleton, 1966
- Dioxycanus Dumbleton, 1966
- Napialus Chu and Wang, 1985
- Hepialiscus Hampson, [1893]
- Parahepialiscus Viette, 1950
- Xhoaphryx Viette, 1953
- Aenetus Herrich-Schäffer, [1858]
- =Charagia Walker, 1856
- =Phloiopsyche Scott, 1864
- =Oenetus; Kirby, 1892
- =Choragia; Pagenstacher, 1909
- =Oenetes; Oke, 1953
- Leto Hübner, [1820]
- =Ecto; Pagenstacher, 1909
- Zelotypia Scott, 1869
- =Xylopsyche Swainson, 1851
- =Leto; auctt
- Oncopera
- =Oncoptera Walker, 1890
- =Paroncopera Tindale, 1933
- =Onchopera; Birket-Smith, 1974
- =Onchoptera; Birket-Smith, 1974
- Trictena Meyrick, 1890
- Bordaia Tindale, 1932
- =Bordaja; Chu and Wang, 1985
- Abantiades Herrich-Schäffer, [1858]
- =Pielus Walker, 1856
- =Rhizopsyche Scott, 1864
- Oxycanus Walker, 1856
- =Porina Walker, 1856
- =Gorina; Quail, 1899
- =Goryna; Quail, 1899
- =Paraoxyxanus Viette, 1950
- Phassodes Bethune-Baker, 1905
Cited literature
References
- Comstock, J.H., (1893). Evolution of the Wings of Insects. The Wilder Quarter Century Book, Ithaca, NY.
- Kristensen, N.P., (1999). The non-Glossatan Moths. Ch. 4, pp. 41–62 in Kristensen, N.P. (Ed.). Lepidoptera, Moths and Butterflies. Volume 1: Evolution, Systematics, and Biogeography. Handbook of Zoology. A Natural History of the phyla of the Animal Kingdom. Band / Volume IV Arthropoda: Insecta Teilband / Part 35: 491 pp. Walter de Gruyter, Berlin, New York.
- Nielsen, E.S., Robinson, G.S. and Wagner, D.L. 2000. Ghost-moths of the world: a global inventory and bibliography of the Exoporia (Mnesarchaeoidea and Hepialoidea) (Lepidoptera) Journal of Natural History, 34(6): 823–878.
External links
- Tree of Life
- Australian Moths Online
- Hepialidae of Australia
- Hepialidae of the World – List of Genera and Links to Species
- LepIndex list of Hepialidae genera and species
- Endoclita and Hepialus pheromones
- Abstract, counterfeit hepialid mummies
- Images of Hepialidae species in New Zealand
- Obituary of Norman B. Tindale
