Attevidae

Attevidae is a family of moths of the Yponomeutoidea superfamily,[1] containing only one genus, Atteva. The group has a pantropical distribution, but at least one species (Atteva aurea) has a range that extends into the temperate zone. No consistent hypotheses regarding the relationships, placement, and ranking of Attevidae have been published, but the prevalent view is that they likely form a monophyletic group within the Yponomeutoidea.[2]

Attevidae
Atteva aurea
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Lepidoptera
Infraorder: Heteroneura
Clade: Eulepidoptera
Clade: Ditrysia
Superfamily: Yponomeutoidea
Family: Attevidae
Genus: Atteva
Walker, 1854
Species

See text

Species

  • Atteva albiguttata - Zeller, 1873
  • Atteva albitarsis - Zeller, 1875
  • Atteva aleatrix - Meyrick, 1922
  • Atteva anisochrysa - Meyrick, 1928
  • Atteva apicalis - Snellen van Vollenhoven, 1863
  • Atteva aurata - Butler, 1882
  • Atteva aurea - (Fitch, 1856)
  • Atteva balanota - Meyrick, 1910
  • Atteva basalis - Snellen van Vollenhoven, 1863
  • Atteva carteri - Walsingham, 1891
  • Atteva charopis - Turner, 1903
  • Atteva chionosticta - Durrant, 1916
  • Atteva conspicua - Walsingham, 1900
  • Atteva cosmogona - Meyrick, 1931
  • Atteva cuprina - Felder, 1875
  • Atteva emissella - Walker, 1863
  • Atteva fabricella - Wallengren, 1861
  • Atteva fabriciella - Swederus, 1787
  • Atteva flavivitta - Walker, 1866
  • Atteva fulviguttata - Zeller, 1873
  • Atteva gemmata - Grote, 1873
  • Atteva heliodoxa - Meyrick, 1910
  • Atteva hesychina - Turner, 1923
  • Atteva holenopla - Diakonoff, 1967
  • Atteva hysginiella - Wallengren, 1861
  • Atteva impariguttata - Zeller, 1877
  • Atteva impunctella - Ritsema, 1875
  • Atteva intermedia - Becker, 2009
  • Atteva iris - Felder, 1875
  • Atteva mathewi - Butler, 1887
  • Atteva megalastra - Meyrick, 1907
  • Atteva modesta - Snellen, 1901
  • Atteva monerythra - Meyrick, 1926
  • Atteva monoplanetis - Meyrick, 1910
  • Atteva niphocosma - Turner, 1903
  • Atteva niveigutta - Walker, 1854
  • Atteva numeratrix - Meyrick, 1930
  • Atteva pastulella - Fabricius, 1787
  • Atteva porphyris - Meyrick, 1907
  • Atteva pulchella - Moore, 1888
  • Atteva pustulella - Fabricius, 1794
  • Atteva pyrothorax - Meyrick, 1928
  • Atteva rawlinsi - Becker, 2009
  • Atteva rex - Butler, 1887
  • Atteva sciodoxa - Meyrick, 1908
  • Atteva scolecias - Meyrick, 1928
  • Atteva siderea - Walsingham, 1891
  • Atteva sidereoides - Becker, 2009
  • Atteva sphaerodoxa - Meyrick, 1918
  • Atteva sphaerotrocha - Meyrick, 1936
  • Atteva subaurata - Durrant, 1900
  • Atteva teratias - Meyrick, 1907
  • Atteva tonseana - Tams, 1935
  • Atteva triplex - Diakonoff, 1967
  • Atteva wallengreni - Sohn & Wu, 2013
  • Atteva yanguifella - Sohn & Wu, 2013
  • Atteva zebra - Duckworth, 1967
  • Atteva zebrina - Becker, 2009

Former species

  • Atteva brucea - Moore, 1859 (synonym of Atteva fabriciella)
  • Atteva niviguttella - Walker, 1863 (synonym of Atteva fabriciella)
gollark: Regardless of what's actually happening with news, you can probably dredge up a decent amount of examples of people complaining about being too censored *and* the other way round.
gollark: With the butterfly-weather-control example that's derived from, you can't actually track every butterfly and simulate the air movements resulting from this (yet, with current technology and algorithms), but you can just assume some amount of random noise (from that and other sources) which make predictions about the weather unreliable over large time intervals.
gollark: That seems nitpicky, the small stuff is still *mostly* irrelevant because you can lump it together or treat it as noise.
gollark: Why are you invoking the butterfly effect here?
gollark: That would fit with the general pattern of governments responding to bad things.

References

  1. van Nieukerken, Erik J.; Lauri Kaila; Ian J. Kitching; Niels P. Kristensen; David C. Lees; Joël Minet; Charles Mitter; Marko Mutanen; Jerome C. Regier; Thomas J. Simonsen; Niklas Wahlberg; Shen-Horn Yen; Reza Zahiri; David Adamski; Joaquin Baixeras; Daniel Bartsch; Bengt Å. Bengtsson; John W. Brown; Sibyl Rae Bucheli; Donald R. Davis; Jurate De Prins; Willy De Prins; Marc E. Epstein; Patricia Gentili-Poole; Cees Gielis; Peter Hättenschwiler; Axel Hausmann; Jeremy D. Holloway; Axel Kallies; Ole Karsholt; Akito Y. Kawahara; Sjaak (J.C.) Koster; Mikhail V. Kozlov; J. Donald Lafontaine; Gerardo Lamas; Jean-François Landry; Sangmi Lee; Matthias Nuss; Kyu-Tek Park; Carla Penz; Jadranka Rota; Alexander Schintlmeister; B. Christian Schmidt; Jae-Cheon Sohn; M. Alma Solis; Gerhard M. Tarmann; Andrew D. Warren; Susan Weller; Roman V. Yakovlev; Vadim V. Zolotuhin; Andreas Zwick (23 December 2011). Zhang, Zhi-Qiang (ed.). "Order Lepidoptera Linnaeus, 1758" (PDF). Zootaxa. Animal biodiversity: An outline of higher-level classification and survey of taxonomic richness. 3148: 212–221. Retrieved 4 November 2012.
  2. Sohn et al. 2013. A Molecular Phylogeny for Yponomeutoidea (Insecta, Lepidoptera, Ditrysia) and Its Implications for Classification, Biogeography and the Evolution of Host Plant Use. PLoS One. 8(1): e55066.


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