This list of 2023 in paleoentomology records new fossilinsecttaxa that are to be described during the year, as well as documents significant paleoentomology discoveries and events which occurred during that year.
Heikkilä et al. (2023) revise purported bombycoid fossil record, reporting that the earliest fossil material that can be assigned to the superfamily with certainty dates to the middle Miocene, while the majority of purported fossil bombycoids lack definitive bombycoid characters.[3]
A member of the family Philopotamidae; a replacement name for Baga Sukatsheva (1992).
Trichopteran research
Baranov et al. (2023) describe leptocerid and lepidostomatid larvae from the Eocene Baltic amber, two of which still bear their cases, and interpret this finding as indicating that at least some aquatic larvae from Baltic amber were trapped in resin flows within the water bodies.[11]
A stem grouplong-legged fly. The type species is E. trisetigerus; genus also includes E. electroechinus, E. falculigerus, E. furcillatus, E. hamatus, E. pankowskii and E. planitibia .
A long-legged fly. Genus includes P. flammea, P. decora, P. elegantula, P. lasciva, P. lepida, P. mustela, & P. vana (all 1907). Published online in 2024, but the issue date is listed as December 2023.
A member of the family Chironomidae belonging to the subfamily Chironominae and the tribe Pseudochironomini. The type species is E. polliciformis; genus also includes E. serpens.
A member of Bibionomorpha belonging to the family Protorhyphidae. The type species is "Vymrhyphus" blagoderovi Krzemiński & Krzemińska (2003); genus also includes new species V. krzeminskorum.
Dipteran research
New fossil material of stratiomyomorphan larvae from the Cretaceous Myanmar amber is reported by Amaral et al. (2023), who interpret the studied fossils as indicating that members of Stratiomyomorpha were not rare, but in fact were common in the Myanmar amber.[36]
Fossil material of a member of the genus Bibio, representing the oldest record of the genus reported to date, is described from the Paleocene Menat Basin (France) by Nel & Kundura (2023).[37]
The type species is P. zhengi Originally described as a member of Pseudogryllotalpidae subsequently assigned to the family Gryllidae by Cadena-Castañeda et al. (2024), who considered P. zhengi to be a junior synonym of Pherodactylus micromorphus.[51]
Moved from Tresdigitus rectanguli Xu, Fang & Wang (2020).[59] Originally described as a mole cricket, but Cadena-Castañeda et al. (2023) considered it to be a member of the family Gryllidae.[58]
The type species is P. scalprata. Originally described as a member of Ensifera and the type genus of the new family Pseudogryllotalpidae; subsequently assigned to the family Gryllidae by Cadena-Castañeda et al. (2024), who considered P. scalprata to be a junior synonym of Pherodactylus micromorphus.[51]
The type species is U. longialatus. Originally described as a member of Ensifera belonging to the family Pseudogryllotalpidae; subsequently assigned to the family Gryllidae by Cadena-Castañeda et al. (2024), who considered U. longialatus to be a junior synonym of Pherodactylus micromorphus.[51]
Orthopteran research
Woodrow, Celiker & Montealegre-Z (2023) study the anatomy of ears and forewings of a specimen of Eomortoniellus handlirschi from the Eocene Baltic amber, estimate the calling song frequency in E. handlirschi, interpret its ear as tuned to the male song frequency but also capable of hearing higher-frequency sounds, and consider this to be possible adaptation to eavesdropping on bat echolocating calls.[62]
The type species is "Notocupes" nigrimonticola Ponomarenko (1968); genus also includes B. caducus (Ponomarenko, 1969), B. dundulaensis (Ponomarenko, 1994), B. foerstery (Ponomarenko, 1968), B. longicoxa (Soriano & Martinez-Delclòs, 2006), B. oculatus (Soriano & Martinez-Delclòs, 2006), B. premeris (Lee et al., 2022), B. spinosus (Li & Cai, 2023) and B. viridis (Soriano & Martinez-Delclòs, 2006).
Originally described as a beetle larva, possibly a member of the family Phoroschizidae/Schizophoridae; argued to be a member of Eumalacostraca of uncertain affinities by Makarov (2024).[74] The type species is C. reichardti.
A collective group name for species belonging to the family Mordellidae and the tribe Mordellini described from the Baltic amber. Includes "Mordella" scheelei Ermisch (1941), "Mordellaria" friedrichi Perkovsky & Odnosum (2013) and "Tomoxia" succinea Bao et al. (2018).
A collective group name for species belonging to the family Mordellidae and the tribe Mordellistenini described from the Baltic amber. Includes "Mordellistena" amplicollis Ermisch (1941), "Mordellistena" antiqua Ermisch (1941), "Mordellistena" goeckei Ermisch (1941), "Mordellistena" korschefskyi Ermisch (1941), "Mordellistena" soror Ermisch (1941) and "Glipostena" sergeli Ermisch (1943), as well as new species B. ultima, B. aurata, B. longistrigata, B. hoffeinsorum, B. concava, B. brevispina and B. atronigra.
A member of Mesophyletinae. The type species is H. plaisiommus. Announced in 2016;[111] Legalov (2023) subsequently republished the description, stating that the journal where the original article was published does not have a printed version, and that the original article lacked information on registration in the ZooBank.[110]
A member of Mesophyletinae. The type species is M. gyralommus. Announced in 2016;[111] Legalov (2023) subsequently republished the description, stating that the journal where the original article was published does not have a printed version, and that the original article lacked information on registration in the ZooBank.[110]
Originally described as a member of the family Kateretidae; subsequently argued to be a sap beetle belonging to the subfamily Apophisandrinae[126] or a member of the separate family Apophisandridae.[88] Genus includes new species P. megacephalus, as well as "Eoceniretes" antiquus Peris & Jelínek.
A collective group name for species belonging to the family Mordellidae and the tribe Mordellistenini described from the Rovno amber. Includes "Glipostena" ponomarenkoi Odnosum & Perkovsky (2009).
Originally described as a soldier beetle belonging to the subfamily Cantharinae and the tribe Cantharini. The type species is T. longelytrum. Kundrata et al. (2023) considered Trapezioceps to be a junior synonym of the mysteriomorphidelateroid genus Mysteriomorphus, though the authors maintained T. longelytrum as a distinct species within the latter genus.[148]
A rove beetle belonging to the subfamily Oxytelinae, possibly a member of the tribe Blediini. Genus includes new species K. makranczyi and K. luminosus.
A member of the family Histeridae belonging to the subfamily Dendrophilinae.
Coleopteran research
Evidence from feathers and larval molts preserved in the Albian amber from the San Just, El Soplao and Peñacerrada I outcrops (Spain), indicating that Cretaceous beetle larvae fed on feathers of avian or nonavian theropods, is presented by Peñalver et al. (2023).[174]
The first known close relative of the Neotropical genus Eohomopterus from the Old World is reported from the Eocene Rovno amber (Ukraine) by Kirichenko-Babko & Perkovsky (2023).[178]
Possible haliplid larvae are described from the Cretaceous amber from Myanmar by Linhart et al. (2023).[179]
Jenkins Shaw, Solodovnikov & Perkovsky (2023) report the discovery of a member of the genus Trichophya (related to the extant species Trichophya antennalis and distinct from Trichophya minor from the amber from Myanmar) from the Upper Cretaceous Taimyr amber from Yantardakh (Russia), documenting the existence of two morphologically different species groups of Trichophya in the Cretaceous.[180]
The first fossil of a member of the genus Proteinus reported to date is described from the Eocene Baltic amber from Denmark by Jenkins Shaw, Bai & Solodovnikov (2023).[181]
Cifuentes-Ruiz et al. (2023) describe an indeterminate ptinid specimen representing the first biological inclusion the Cenomanian amber from the Dexter Member of the Woodbine Group (Texas, United States) reported to date.[182]
Zippel et al. (2023) describe cucujiform (possibly endomychid) larvae from the Cretaceous Burmese amber and Miocene Mexican amber, interpreted as possible fungus-eaters on rotting wood.[183]
A Cimbicidsawfly The type species is L. brevilatum; genus also includes L. alaemacula, L. fasciatum, L. longiclava, L. longipallidum, L. longitenebricum and L. proxivena.
A study on the ecology of haidomyrmecine ants is published by Sosiak et al. (2023), who interpret the studied ants as primarily leaf litter or ground-nesting and foraging predators, find support for specialized predation in several haidomyrmecine genera, and argue that the extinction of haidomyrmecines may have resulted in a vacant ecospace that was subsequently filled by members of modern ant lineages with trap-jaw like morphology and behavior.[232]
A member of the family Braconidae belonging to the subfamily Doryctinae. The type species is P. kanti; genus also includes "Doryctomorpha" tertiaria Brues (1933).
A member of Ithonoidea of uncertain affinities. The type species is Y. splendidus.
Neuropteran research
The oldest dustywing-type larva reported to date is described from the Cretaceous amber from Myanmar by Haug & Haug (2023).[278]
Mengel et al. (2023) describe new nevrorthid larvae from the Cretaceous amber from Myanmar and from the Eocene Baltic amber, and study on the morphological diversity of nevrorthid larvae, reporting the existence of fossil larvae with morphologies that are now extinct.[279]
New fossil material of long-nosed antlion larvae, mostly from the Cretaceous Myanmar amber (and two specimens from the Eocene Baltic amber), is described by Hassenbach et al. (2023), who interpret the studied fossils as confirming that the morphological diversity of Cretaceous silky lacewings was much higher than the diversity of their extant relatives.[280]
A study on the diversity of lacewing larvae with tooth-bearing mouthparts, based on data from new specimens from the Cretaceous Myanmar amber, is published by Braig et al. (2023), who interpret their findings as indicative of greater morphological diversity of the Cretaceous larvae than extant larvae, as well as indicative of convergent evolution resulting in partial reappearance of morphologies that went extinct after the Cretaceous.[281]
A mayfly, the type genus of the new family Siphlonephemerellidae within the superfamily Siphlonuroidea. Genus includes new species S. mupengxui.
Ephemeropteran research
A study on the diversity of mayflies throughout their evolutionary history is published by Sroka, Godunko & Prokop (2023), who interpret their findings as indicative of a major extinction of mayflies in the mid-Cretaceous which was likely connected to the rise of the flowering plants.[291]
A protozygopteran belonging to the family Progoneuridae. The type species is I. marilevorum. Published online in 2024, but the issue date is listed as December 2023.
A protozygopteran belonging to the family Voltzialestidae. Genus includes new species P. elegans and P. parva. Published online in 2024, but the issue date is listed as December 2023.
A protozygopteran belonging to the family Voltzialestidae. The type species is P. dubia. Published online in 2024, but the issue date is listed as December 2023.
A protozygopteran belonging to the family Permagrionidae. Genus includes new species T. sakmarensis and T. mutovkensis. Published online in 2024, but the issue date is listed as December 2023.
A dragonfly belonging to epiproctophoran stem group of Anisoptera.
Odonatopteran research
A study on trends in morphological diversity of Permian to Jurassic members of Odonata is published by Deregnaucourt et al. (2023), who report evidence of decreasing morphological diversity through time in spite of increasing species richness, as well evidence of significant changes in morphological diversity at the Permian-Triassic and Triassic-Jurassic transitions.[310]
A froghopper, possibly a member of the family Sinoalidae. The type species is A. leptosomus. Chen et al. (2024) considered Araeoanasillus to be a junior synonym of the sinoalid genus Cretadorus, though the authors maintained A. leptosomus as a distinct species within the latter genus.[317]
Fossil material of a member of the genus Aphelocheirus, representing the oldest record of the family Aphelocheiridae reported to date, is described from the Lower Eocene Palana Formation (Rajasthan, India) by Patel et al. (2023).[361]
New fossil material of the archijassid species Kisa fasciata is described from the Jurassic Yangshuzhuang and Yan'an formations (China) by Fu et al. (2023), expanding known distribution of Archijassidae in Eurasia and providing evidence of a considerable intraspecific variation of K. fasciata.[362]
Evidence from new immature earwig specimens from the Cretaceous amber from Myanmar, interpreted as indicative of reduction of morphological diversity of grasping apparatuses of earwigs over the past 100 million years, is presented by Haug et al. (2023).[369]
A member of "Eoblattodea" (paraphyletic grouping of cockroach-like insects related to dictyopterans), the type genus of the new family Ensiferoblattidae. The type species is E. oecanthoides.
A stem-dictyopteran belonging to the family Gyroblattidae. Moved from Etoblattina clarkii Scudder (1893).
Khramov, Foraponova & Węgierek (2023) describe specimens of Tillyardembia from the Permian locality Chekarda (Perm Krai, Russia) preserved with pollen on their heads, thoraces, legs and abdomens, representing the oldest record of pollen-bearing insects reported to date.[385]
Haug et al. (2023) describe a holometabolan larva (probably a new specimen of ?Partisaniferus edjarzembowskii) from the Cretaceous Burmese amber, preserved with the mouthparts forming a beak and with a large and inflated trunk, and interpret the studied larva as physogastric and possibly living in confined spaces inside wood.[386]
General research
A study on the taxonomic diversity of insects throughout the Permian and Triassic, providing evidence of more than one extinction events accompanied by significant diversity drop and faunal turnovers, is published by Gui, Liu & Tian (2023).[387]
Solórzano‑Kraemer et al. (2023) report the preservation of phorid flies (but not fly larvae) associated with the holotype of Oculudentavis naga from the Cretaceous Myanmar amber, and interpret this finding as preserving early stage of scavenging by flies; the authors also note that there is not evidence of scavenging by ants from the Myanmar amber, and interpret it as suggesting that the Cretaceous ants did not yet have a foraging strategy to search for vertebrate corpses and to eat carrion.[388]
Review of anti-predator strategies of holometabolan larvae from the Cretaceous ambert from Myanmar is published by Haug et al. (2023), who find evidence of repeated independent evolution of strategies employed by extant insects, and report the discovery of a new leaf-mining hymenopteran caterpillar and a hangingfly caterpillar with extensive spines.[389]
An assemblage of chironomid (referrable to extant subfamilies), mayfly and lepidopteran fossils, closer in composition to Cenozoic insect assemblages than to Mesozoic ones, is described from the Upper Cretaceous (Maastrichtian) Chorrillo Formation (Argentina) by Vera et al. (2023).[390]
A diverse insect assemblage, including representatives of the orders Coleoptera, Diptera, Hymenoptera, Orthoptera and Hemiptera, is described from the Miocene shales from Wang Kaew in the Mae Sot basin (Thailand) by Warapeang et al. (2023).[391]
Evidence from thermal maturation experiments on extant beetles, interpreted as indicating that colour patterns preserved in fossil insect specimens can be plausibly explained as biological in origin and represent melanin-based color patterns, is presented by Wang et al. (2023).[392]
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^Xu, C.; Fang, Y.; Fang, Y.; Wang, H.; Zhou, Q.; Jiang, X.; Zhang, H. (2023). "Early Jurassic orthopteran insects from the southern Junggar Basin, NW China, with discussion of biodiversity changes of Orthoptera across the Triassic–Jurassic boundary". In J. Sha; S. M. Slater; V. Vajda; P. E. Olsen; H. Zhang (eds.). The Triassic and Jurassic of the Junggar Basin, China: Advances in Palaeontology and Environments. Geological Society, London, Special Publications. Vol. 538. The Geological Society of London. pp. 147–154. doi:10.1144/SP538-2021-184. S2CID257995730.
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