Palaeontinidae

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Palaeontinidae
Temporal range: Late Triassic-Early Cretaceous Norian–Aptian
Synapocossus sciacchitanoae
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hemiptera
Suborder: Auchenorrhyncha
Infraorder: Cicadomorpha
Superfamily: Palaeontinoidea
Family: Palaeontinidae
Handlirsch, 1906
Type genus
Palaeontina
Butler, 1873
Genera

See text

Synonyms

CicadomorphidaeEvans, 1956

Palaeontinidae, commonly known as giant cicadas, is an

extinct family of cicadomorphs. They existed from the Late Triassic to the Early Cretaceous. The family contains around 30 to 40 genera and around a hundred species.[1]

Discovery

The first palaeontinid discovered was

entomologist Arthur Gardiner Butler in his book Lepidoptera Exotica; or, Descriptions and Illustrations of Exotic Lepidoptera. Butler claimed that it was the oldest butterfly ever recovered, having mistakenly identified it as a butterfly of the family Nymphalidae.[3]

Description and paleobiology

Palaeontinids had large bodies covered with bristles (

setae). They had small heads and broad wings. They superficially resemble moths.[4][5] Large palaeontinids like Colossocossus had forewings that reached the length of 57 to 71 mm (2.2 to 2.8 in).[6]
They possessed an inflated
frons and a long rostrum (piercing and sucking mouthpart), indicating that they fed on xylem fluids like some other modern hemipterans.[7]

Some authors have proposed that the

theropods, primitive mammals, and early birds) may have also contributed significantly to their extinction.[8]

Most species of palaeontinids exhibit

secondary sexual characteristics. The color patterns can vary slightly within the same species.[7]

Palaeontinids, like modern cicadas, possess four membranous wings supported by veins. The length and width ratio of the wings can vary within the same species, sometimes as a result of fossil preservation.[7] Early Jurassic palaeontinids, like Suljuktocossus, exhibit the most primitive wing forms in the family.[10] The forewing was elliptical with the "nodal line" (the area where the wing bends during flight, also known as the "transverse flexion line") more or less dissecting through the center of the wing. The hindwing was short and broad. The bases of the forewings overlapped that of the hindwings like in modern butterflies. Taken together with their large bodies, these characteristics indicate that they were fast but moderately versatile fliers.[11]

In contrast, later palaeontinids like the Upper Jurassic

sphinx moths.[11] They also possessed changes to the leading edge of their forewings, suggesting an overall gain in lift.[10]

The trend of forewing elongation is most evident in members of the family Mesogereonidae, an early offshoot and close relatives of palaeontinids.[12]

Classification

Early Jurassic palaeontinids[2]

The family was first erected by the

Austrian entomologist Anton Handlirsch in 1908. Like Butler, Handlirsch insisted that palaeontinids were members of lepidopteran Heteroneura (butterflies and moths). Palaeontinids were then only known mostly from poorly preserved specimens like Palaeontina and Eocicada. He claimed they were related to the extant family Limacodidae (slug moths).[13] The English entomologist Edward Meyrick supported the lepidopteran conclusion, though he believed they belonged to the family Hepialidae (ghost moths) instead. He said "There is little doubt that it [i.e. Palaeontina oolitica] belongs to the Hepialidae."[2]

The

Australian entomologist and geologist Robert John Tillyard supported Lameere's conclusion, noting that the wings of palaeontinid fossils lacked the characteristic scales of lepidopterans but instead had tubercules, pits, and cross-ridges like those found in modern cicadas.[13] He also cited characteristics of wing venation that distinctly differs from that of lepidopterans.[2]

Palaeontinidae are currently classified under the extinct superfamily

The name Cicadomorphidae was once proposed as a replacement for the name Palaeontinidae in 1956 by the Australian entomologist J.W. Evans. This was because of Handlirsch's earlier insistence that the type species Palaeontina oolitica may not have been Hemipteran. However, Evans later conceded that retaining the name Palaeontinidae was preferable as the drawings Handlirsch based his conclusions on were from badly preserved specimens.[15]

Evolution

Riek (1976) originally considered Palaeontinoidea to be the descendants of the family Cicadoprosbolidae (currently known as the family Tettigarctidae), insects believed to be transitional between the ancestral cicada-like family Prosbolidae and the modern family Cicadidae.[10]

Wang et al (2009), however, notes that palaeontinoids more closely resemble prosbolids in agreement with earlier studies by Wootton (1971), Shcherbakov (1984), and Shcherbakov and Popov (2002). They conclude that palaeontinoids descended directly from the family Prosbolidae rather than from tettigarctids.[10] Modern cicadas therefore, did not descend directly from Palaeontinidae.

Within Palaeontinoidea, the family Dunstaniidae (

Lower Jurassic of Australia, South Africa, and China) is ancestral to palaeontinids. Both are distinct from the only other member of the superfamily, the more primitive and specialized family Mesogereonidae (Upper Triassic of Australia and South Africa).[10]

Distribution and geologic time range

The oldest known member of the group is

Lower Cretaceous (~115-113 Mya).[8][14] They achieved their greatest diversity during the Jurassic period.[17]

Palaeontinid fossils are abundant in

Genera

The following is the list of genera classified under Palaeontinidae:[19]

See also

References

  1. ^ "Family Palaeontinidae". The EDNA Fossil Insect Database. Retrieved July 16, 2011.
  2. ^ a b c d e R.J. Tillyard (1919). "The Panorpoid Complex 3" (PDF). Proceedings of the Linnean Society of New South Wales (44): 533–718.
  3. ^ Arthur Gardiner Butler (1869–1874). Lepidoptera Exotica; or, Descriptions and Illustrations of Exotic Lepidoptera. E. W. Jansen. pp. 126–127.
  4. ^
    ISSN 1175-5326
    . Retrieved July 13, 2011.
  5. . Retrieved July 15, 2011.
  6. ^ . Retrieved July 15, 2011.
  7. ^ . Retrieved July 15, 2011.
  8. ^ . Retrieved July 15, 2011.
  9. ^ D. E. Shcherbakov (2000). "Permian Faunas of Homoptera (Hemiptera) in Relation to Phytogeography and the Permo-Triassic Crisis" (PDF). Paleontological Journal. 34 (Suppl. 3): S251–S267. Retrieved July 15, 2011.
  10. ^ .
  11. ^ . Retrieved July 15, 2011.
  12. ^ R. Wootton (1971). "The Evolution of Cicadoidea (Homoptera)" (PDF). Proceedings: XIII International Congress of Entomology, Moscow (1): 318–319. Retrieved July 15, 2011.
  13. ^ . Retrieved July 15, 2011.
  14. ^ a b "Palaeontinidae". Paleobiology Database. Retrieved July 15, 2011.
  15. ISSN 0066-4170
    . Retrieved July 21, 2011.
  16. ^ .
  17. ^ Kyoichiro Ueda (1996). "A New Palaeontinid Species from the Lower Cretaceous of Brazil (Homoptera: Palaeontinidae)" (PDF). Bulletin of the Kitakyushu Museum of Natural History. 16. Kitakyushu Museum and Institute of Natural History: 99–104. Retrieved July 21, 2011.
  18. ^ Xavier Martínez-Delclòs (1990). "Insectos del Cretácico inferior de Santa Maria de Meià (Lleida): Colección Lluís Maria Vidal i Carreras" (PDF). Treballs del Museu de Geología de Barcelona (in Spanish). 1. Museo de Geología de Barcelona: 91–116. Retrieved July 21, 2011.
  19. ^ Mikko Haaramo (May 5, 2009). "†Palaeontinidae: After Grimaldi & Engel, 2005, Wang, Zhang & Fang, 2006, and Wang, Zhang & Szwedo, 2009". Mikko's Phylogeny Archive. Retrieved July 15, 2011.
  20. S2CID 129712238
    . Retrieved July 13, 2011.

External links