Prehistoric Lepidoptera

Prehistoric Lepidoptera are both butterflies and moths that lived before recorded history. The fossil record for Lepidoptera is lacking in comparison to other winged species, and tending not to be as common as some other insects in the habitats that are most conducive to fossilization, such as lakes and ponds, and their juvenile stage has only the head capsule as a hard part that might be preserved. Yet there are fossils, some preserved in amber and some in very fine sediments. Leaf mines are also seen in fossil leaves, although the interpretation of them is tricky.[1] Putative fossil stem group representatives of Amphiesmenoptera (the clade comprising Trichoptera and Lepidoptera) are known from the Triassic.[2]:567

1887 engraving of Prodryas persephone, a fossil lepidopteran from the Eocene

Previously, the earliest known lepidopteran fossils were three wings of Archaeolepis mane, a primitive moth-like species from the Jurassic, about 190 million years ago, found in Dorset, UK, which show scales with parallel grooves under a scanning electron microscope and a characteristic wing venation pattern shared with Trichoptera (caddisflies).[3][4] In 2018, the discovery of exquisite fossilised scales from the Triassic-Jurassic boundary were reported in the journal Science Advances. They were found as rare palynological elements in the sediments of the Triassic-Jurassic boundary from the cored Schandelah-1 well, drilled near Braunschweig in northern Germany. This pushes back the fossil record and origin of glossatan lepidopterans by about 70 million years, supporting molecular estimates of a Norian (c. 212 million years) divergence of glossatan and non-glossatan lepidopterans. The authors of the study proposed that lepidopterans evolved a proboscis as an adaptation to drink from droplets and thin films of water for maintaining fluid balance in the hot and arid climate of the Triassic.[5]

Only two more sets of Jurassic lepidopteran fossils have been found, as well as 13 sets from the Cretaceous, which all belong to primitive moth-like families.[1] Many more fossils are found from the Cenozoic, and particularly the Eocene Baltic amber. The oldest genuine butterflies of the superfamily Papilionoidea have been found in the Early Eocene (Ypresian) MoClay or Fur Formation of Denmark. The best preserved fossil lepidopteran is considered to be the Eocene Prodryas persephone from the Florissant Fossil Beds.[6][7]

Phylogeny

Phylogenetic hypothesis of major lepidopteran lineages superimposed on the geologic time scale. Radiation of angiosperms spans 130–95 mya from their earliest forms to domination of vegetation.

Lepidoptera and Trichoptera (caddisflies) are more closely related than any other taxa, sharing many similarities that are lacking in other insect orders; for example the females of both orders are heterogametic, meaning they have two different sex chromosomes, whereas in most species the males are heterogametic and the females have two identical sex chromosomes. The adults in both orders display a particular wing venation pattern on their forewings. The larvae of both orders have mouth structures and a gland with which they make and manipulate silk. Willi Hennig grouped the two orders into the Amphiesmenoptera superorder; they are sisters, and together are sister to the extinct order Tarachoptera.[8]

Micropterigidae, Agathiphagidae and Heterobathmiidae are the oldest and most basal lineages of Lepidoptera. The adults of these families do not have the curled tongue or proboscis, that are found in most members order, but instead have chewing mandibles adapted for a special diet. Micropterigidae larvae feed on leaves, fungi, or liverworts (much like the Trichoptera).[9] Adult Micropterigidae chew the pollen or spores of ferns. In the Agathiphagidae, larvae live inside kauri pines and feed on seeds. In Heterobathmiidae the larvae feed on the leaves of Nothofagus, the southern beech tree. These families also have mandibles in the pupal stage, which help the pupa emerge from the seed or cocoon after metamorphosis.[9]

The Eriocraniidae have a short coiled proboscis in the adult stage, and though they retain their pupal mandibles with which they escaped the cocoon, their mandibles are non-functional thereafter.[9] Most of these non-ditrysian families, are primarily leaf miners in the larval stage. In addition to the proboscis, there is a change in the scales among these basal lineages, with later lineages showing more complex perforated scales.[1]

With the evolution of the Ditrysia in the mid-Cretaceous, there was a major reproductive change. The Ditrysia, which comprise 98% of the Lepidoptera, have two separate openings for reproduction in the females (as well as a third opening for excretion), one for mating, and one for laying eggs. The two are linked internally by a seminal duct. (In more basal lineages there is one cloaca, or later, two openings and an external sperm canal.) Of the early lineages of Ditrysia, Gracillarioidea and Gelechioidea are mostly leaf miners, but more recent lineages feed externally. In the Tineoidea, most species feed on plant and animal detritus and fungi, and build shelters in the larval stage.[1]

The Yponomeutoidea is the first group to have significant numbers of species whose larvae feed on herbaceous plants, as opposed to woody plants.[1] They evolved about the time that flowering plants underwent an expansive adaptive radiation in the mid-Cretaceous, and the Gelechioidea that evolved at this time also have great diversity. Whether the processes involved co-evolution or sequential evolution, the diversity of the Lepidoptera and the angiosperms increased together.

In the so-called "macrolepidoptera", which constitutes about 60% of lepidopteran species, there was a general increase in size, better flying ability (via changes in wing shape and linkage of the forewings and hindwings), reduction in the adult mandibles, and a change in the arrangement of the crochets (hooks) on the larval prolegs, perhaps to improve the grip on the host plant.[1] Many also have tympanal organs, that allow them to hear. These organs evolved eight times, at least, because they occur on different body parts and have structural differences.[1] The main lineages in the macrolepidoptera are the Noctuoidea, Bombycoidea, Lasiocampidae, Mimallonoidea, Geometroidea and Rhopalocera. Bombycoidea plus Lasiocampidae plus Mimallonoidea may be a monophyletic group.[1] The Rhopalocera, comprising the Papilionoidea (butterflies), Hesperioidea (skippers), and the Hedyloidea (moth-butterflies), are the most recently evolved.[9] There is quite a good fossil record for this group, with the oldest skipper dating from 56 million years ago.[1]

Fossil Lepidoptera taxa

This is a list of all described fossil Lepidoptera species.[10][11][12][13][14][15]

Taxa marked with † are extinct

Family Saturniidae

  • Rothschildia Grote, 1896
    • Rothschildia fossilis Cockerell, 1914 (originally in Attacus)

Family Sphingidae

Family Copromorphidae

Family Cossidae

Family †Eolepidopterigidae

Family Eriocraniidae

Family Autostichidae

Family Elachistidae

Family Ethmiidae

  • Ethmia Hübner, [1819]
    • Ethmia mortuella Scudder, 1890 (Colorado, Florissant)

Family Oecophoridae

  • Borkhausenites Rebel, 1934
    • Borkhausenites angustipenella Rebel, 1935
    • Borkhausenites bachofeni Rebel, 1934
    • Borkhausenites crassella Rebel, 1935
    • Borkhausenites implicatella Rebel, 1935
    • Borkhausenites incolumella Rebel, 1934
    • Borkhausenites ingentella Rebel, 1935
    • Borkhausenites vulneratella Rebel, 1935
  • Depressarites Rebel, 1936
    • Depressarites blastuliferella Rebel, 1935
    • Depressarites levipalpella Rebel, 1935
  • Epiborkhausenites Skalski, 1973 (Bartonian, Baltic amber, Lithuania)
    • Epiborkhausenites obscurotrimaculatus Skalski, 1973
  • Glesseumeyrickia Kusnezov, 1941
    • Glesseumeyrickia henrikseni Kusnezov, 1941
  • Hexerites Cockerell, 1933 (originally in Thyrididae)
  • Microsymmocites Skalski, 1977
    • Microsymmocites Skalski, 1977
  • Neoborkhausenites Skalski, 1977
    • Neoborkhausenites incertella (Rebel, 1935) (originally in Borkhausenites)
  • Palaeodepressaria Skalski, 1979
    • Palaeodepressaria hannemanni Skalski, 1979
    • Paraborkhausenites Kusnezov, 1941
    • Paraborkhausenites innominatus Kusnezov, 1941
    • Paraborkhausenites vicinella (Rebel, 1935) (originally in Borkhausenites)

Family Symmocidae

Family Geometridae

Hydriomena? protrita holotype forewing

Family Bucculatricidae

  • Bucculatrix Zeller, 1839
    • Bucculatrix platani Kozlov, 1988 (Kazakhstan, Late Cretaceous)

Family Gracillariidae

Family Hepialidae

Family Adelidae

  • Adela Latreille, 1796
    • Adela kuznetzovi Kozlov, 1987
    • Adela similis Kozlov, 1987
  • Adelites Rebel 1934
    • Adelites electrella Rebel, 1934
    • Adelites purpurascens Rebel, 1935
    • Adelites serraticornella Rebel, 1935
    • An undescribed †Adelites species

Family Incurvariidae

Family Micropterigidae

Family Nepticulidae

Family Arctiidae

Family Lymantriidae

Family Noctuidae

  • Noctuites Heer, 1849
    • Noctuites haidingeri Heer, 1849 (Croatia, Radoboj, Cenozoic)
  • Xyleutites Kozhanchikov, 1957

Family Notodontidae

  • Cerurites Kernbach, 1967
    • Cerurites wagneri Kernbach, 1967 (Germany, Willershausen, Cenozoic)

Basal or incertae sedis

Family Hesperiidae

  • Pamphilites Scudder, 1875
  • Thanatites Scudder, 1875
    • Thanatites vetula (Heyden, 1859) (Western Germany, Cenozoic) (originally in Nymphalidae)

Family Lycaenidae

  • Aquisextana Theobald, 1937
    • Aquisextana irenaei Theobald, 1937 (France, Early Oligocene)

Family Nymphalidae

  • Apanthesis Scudder, 1889
    • Apanthesis leuce Scudder, 1889 (Colorado, Florissant)
  • Barbarothea Scudder, 1892
    • Barbarothea florissanti Scudder, 1892 (Colorado, Florissant)
  • Doxocopa Hübner, 1819
    • Doxocopa wilmattae (Cockerell, 1907) (Colorado, Florissant) (originally in Chlorippe)
  • Hestina Westwood, 1850
  • Jupitellia Carpenter, 1985
    • Jupitellia charon (Scudder, 1889) (originally in Jupiteria)
  • Lethites Scudder, 1875
    • Lethites reynesii (Scudder, 1872)
  • Undescribed Limenitis species
  • Mylothrites Scudder, 1875
  • Neorinella Martins, Kucera-Santos, Vieira & Fr, 1993
    • Neorinella garciae Martines-Neto, 1993
  • Neorinopis Butler, 1873
    • Neorinopis sepulta (Boisduval, 1840) (France, Early Oligocene)
  • Nymphalites Scudder, 1889
    • Nymphalites obscurum Scudder, 1889 (Colorado, Florissant)
    • Nymphalites scudderi Beutenmller and Cockerell, 1908
    • Nymphalites zeuneri Jarembowski, 1980
  • Prodryas Scudder, 1878
  • Prolibythea Scudder, 1889
    • Prolibythea vagabunda Scudder, 1889 (Colorado, Florissant)
  • Vanessa Fabricius, 1807
    • Vanessa amerindica Miller & Brown, 1989 (Colorado, Florissant)

Family Papilionidae

Family Pieridae

  • Coliates Scudder, 1875
    • Coliates proserpina Scudder, 1875
  • Oligodonta Brown, 1976
    • Oligodonta florissantensis Brown, 1976 (Colorado, Oligocene)
  • Pontia Fabricius, 1807
    • Pontia freyeri (Heer, 1849)
  • Stolopsyche Scudder, 1889
    • Stolopsyche libytheoides Scudder, 1889 (Colorado, Cenozoic)

Family Riodinidae

Family Pterophoridae

Family Pyralidae

Family Castniidae

Family Psychidae

  • Dahlica Enderlein, 1912
  • Palaeopsyche Sobczyk & Kobbert, 2009
    • Palaeopsyche secundum Sobczyk & Kobbert, 2009 (Baltic amber)
    • Palaeopsyche transversum Sobczyk & Kobbert, 2009 (Baltic amber)
  • Psychites Kozlov, 1989
    • Psychites pristinella Kozlov, 1989 (Baltic region, Cenozoic, amber)
  • Siederia Meier, 1957
  • Sterrhopterix Hübner, 1825
    • Sterrhopteryx pristinella Rebel, 1934
  • Taleporia Hübner, 1825
  • Bacotia Tutt, 1899

Family Tineidae

  • Architinea Rebel, 1934
    • Architinea balticella Rebel, 1934
    • Architinea sepositella Rebel, 1934
  • Dysmasiites Kusnezov, 1941
    • Dysmasiites carpenteri Kusnezov, 1941
  • Electromeessia Kozlov, 1987
    • Electromeessia zagulijaevi Kozlov, 1987 (Baltic region, Eocene amber)
  • Glessoscardia Kusnezov, 1941
    • Glessoscardia gerasimovi Kusnezov, 1941
  • Martynea Kusnezov, 1941
    • Martynea rebeli Kusnezov, 1941
  • Monopibaltia Skalski, 1974
    • Monopibaltia ignitella Skalski, 1974 (Baltic region, Eocene amber)
  • Palaeoinfurcitinea Kozlov, 1987
    • Palaeoinfurcitinea rohdendorfi Kozlov, 1987 (Russia, Eocene amber)
  • Palaeoscardiites Kusnezov, 1941
    • Palaeoscardiites mordvilkoi Kusnezov, 1941
  • Palaeotinea Kozlov, 1987
    • Palaeotinea rasnitsyni Kozlov, 1987
  • Paratriaxomasia Jarzembowski, 1980
    • Paratriaxomasia solentensis Jarzembowski, 1980
  • Proscardiites Kusnezov, 1941
    • Proscardiites martynovi Kusnezov, 1941
  • Pseudocephitinea Kozlov, 1987
    • Pseudocephitinea svetlanae Kozlov, 1987 (Russia, Eocene amber)
  • Scardiites Kusnezov, 1941
    • Scardiites meyricki Kusnezov, 1941
  • Simulotenia Skalski, 1977
    • Simulotenia intermedia Skalski, 1977
  • Tillyardinea Kusnezov, 1941
    • Tillyardinea eocaenica Kusnezov, 1941
  • Tinea Linnaeus, 1758
    • Tinea antique Rebel, 1822
  • Tineitella T. B. Fletcher, 1940
    • Tineitella crystalli Kawall, 1876 (originally in Tineites)
    • Tineitella sucinacius Kozlov, 1987 (originally in Tineites)
  • Tineolamima Rebel, 1934
    • Tineolamima aurella Rebel, 1934
  • Tineosemopsis Skalski, 1974
    • Tineosemopsis decurtatus Skalski, 1974

Family Tortricidae

Antiquatortia histuroides
Electresia zalesskii
Tortricidrosis inclusa
  • Antiquatortia
    • Antiquatortia histuroides Brown & Baixeras, 2018 (Dominican amber)
  • Electresia Kusnezov, 1941
    • Electresia zalesskii Kusnezov, 1941 (Tanzania, Copal)
  • Tortricibaltia Skalski, 1992
    • Tortricibaltia diakonoffi Skalski, 1981 (Baltic amber)
  • Tortricidrosis Skalski, 1973
    • Tortricidrosis inclusa Skalski, 1973 (Baltic amber)

Family Heliodinidae

  • Baltonides Skalski, 1981
    • Baltonides roeselliformis Skalski, 1981 (Baltic region, Late Eocene)

Family Lyonetiidae

Family Yponomeutidae

  • Epinomeuta Rebel, 1936
    • Epinomeuta truncatipennella Rebel, 1936

Family Zygaenidae

Family †Archaeolepidae

Family †Curvicubitidae

  • Curvicubitus Hong, 1984
    • Curvicubitus triassicus Hong, 1984 (China, Middle Triassic)

Family †Mesokristenseniidae

Superfamily unassigned

Paleolepidopterites destructus
Paleolepidopterites florissantanus

Excluded from Lepidoptera

Several fossils originally described as lepidopterans have subsequently been assigned to other groups, some as basal Amphiesmenoptera, others into other entirely distinct insect orders.[16]

Family †Eocoronidae

Family †Palaeontinidae (?)

Family †Permochoristidae

Family †Choristopsychidae

From the late middle Jurassic (164-165 mya) from the Daohugou fossil beds of Inner Mongolia.[17]

  • Choristopsyche Martynov, 1937[17]
    • Choristopsyche tenuinervis Martynov, 1937[17]
    • Choristopsyche perfecta Qiao, Shih, Petrulevičius & Ren Dong, 2013[17]
    • Choristopsyche asticta Qiao, Shih, Petrulevičius & Ren Dong, 2013[17]
  • Paristopsyche Qiao, Shih, Petrulevičius & Ren Dong, 2013[17]
    • Paristopsyche angelineae Qiao, Shih, Petrulevičius & Ren Dong, 2013[17]

See also

References

  1. Grimaldi, D. and Engel, M. S. (2005). Evolution of the Insects. Cambridge University Press. ISBN 978-0-521-82149-0.CS1 maint: multiple names: authors list (link)
  2. Powell, Jerry A. (2009). "Lepidoptera". In Resh, Vincent H.; Cardé, Ring T. (eds.). Encyclopedia of Insects (2 (illustrated) ed.). Academic Press. pp. 557–587. ISBN 978-0-12-374144-8. Retrieved 14 November 2010.
  3. Grimaldi, David A.; Michael S. Engel (2005). Evolution of the insects. Cambridge University Press. p. 561. ISBN 978-0-521-82149-0.
  4. Davies, Hazel; Butler, Carol A. (June 2008). Do butterflies bite?: fascinating answers to questions about butterflies and moths. Rutgers University Press. p. 48. ISBN 978-0-8135-4268-3. Retrieved 15 July 2011.
  5. van Eldijk, Timo J. B.; Wappler, Torsten; Strother, Paul K.; van der Weijst, Carolien M. H.; Rajaei, Hossein; Visscher, Henk; van de Schootbrugge, Bas (10 January 2018). "A Triassic-Jurassic window into the evolution of Lepidoptera". Science Advances. 4 (1): e1701568. Bibcode:2018SciA....4E1568V. doi:10.1126/sciadv.1701568. PMC 5770165. PMID 29349295.
  6. Meyer, Herbert William; Smith, Dena M. (2008). Paleontology of the Upper Eocene florissant formation, Colorado. Geological Society of America. p. 6. ISBN 978-0-8137-2435-5. Retrieved 15 July 2011.
  7. Unacknowledged. "Lepidoptera – latest classification". Discoveries in Natural History & Exploration. University of California. Retrieved 15 July 2011.
  8. Wolfram Mey; Wilfried Wichard; Patrick Müller; Bo Wang (2017). "The blueprint of the Amphiesmenoptera – Tarachoptera, a new order of insects from Burmese amber (Insecta, Amphiesmenoptera)". Fossil Record. 20 (2): 129–145. doi:10.5194/fr-20-129-2017.
  9. Scoble, Malcolm J. (September 1995). "2". The Lepidoptera: Form, Function and Diversity (1 ed.). Oxford University: Oxford University Press. pp. 4–5. ISBN 978-0-19-854952-9.
  10. Fidel Fernández-Rubio (1999). "Las mariposas fósiles. Razones de su escasez y su influencia sobre el conocimiento de la filogenia y distribución de Zygaenini (Lepidoptera: Zygaenidae)" [Fossil butterflies. Causes of their rarity and how they influence our knowledge of phylogeny and distribution of Zygaenini (Lepidoptera: Zygaenidae)] (PDF). Boletín de la S.E.A. 26: 521–532.
  11. Niels P. Kristensen (3 December 1998). Handbuch der Zoologie: eine Naturgeschichte der Stämme des Tierreiches. Walter de Gruyter. pp. 19–. ISBN 978-3-11-015704-8. Retrieved 25 July 2011.
  12. leptree. Webcache.googleusercontent.com (2011-05-18). Retrieved on 2011-07-25.
  13. Thomas Sobczyk & Max J. Kobbert (2009). "Die Psychidae des baltischen Bernsteins" (PDF). Nota Lepidopterologica. 32 (1): 13–22. Archived from the original (PDF) on 20 March 2012.
  14. Lepidoptera Genera. Nhm.ac.uk. Retrieved on 2011-07-25.
  15. Beccaloni, George; et al. (February 2005). "Scientific name search". The Global Lepidoptera Names Index. Natural History Museum, London.
  16. Sohn, Jae-Cheon; Conrad Labandeira; Donald Davis; Charles Mitter (2012). An annotated catalog of fossil and subfossil Lepidoptera (Insecta : Holometabola) of the world (PDF). Zootaxa. Auckland, N.Z.: Magnolia Press. pp. 1–132. ISBN 978-1-86977-888-0.
  17. Qiao X, Shih CK, Petrulevičius JF, Ren Dong R (2013). "Fossils from the Middle Jurassic of China shed light on morphology of Choristopsychidae (Insecta, Mecoptera)". ZooKeys (318): 91–111. doi:10.3897/zookeys.318.5226. PMC 3744206. PMID 23950679. Retrieved 29 July 2013.
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