This list of 2024 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.
Frese, McCurry & Wells (2024) describe pupae and uncased larvae of caddisflies from the Miocene McGraths FlatLagerstätte (Australia), including specimens with large compound eyes preserving details of the rhabdoms and corneal nanocoating and with other external and internal structures, and interpret the environment of the studied caddisflies as affected by cyclic catastrophic events.[16]
A member of the family Stratiomyidae belonging to the subfamily Stratiomyinae and the tribe Prosopochrysini. Genus includes C. dominicana from the Dominican amber and C. kraemerae from the Mexican amber.
A member of the family Dolichopodidae. Genus includes P. flammea (Meunier, 1907), P. mustela (Meunier, 1907), P. decora (Meunier, 1907), P. elegantula (Meunier, 1907), P. vana (Meunier, 1907), P. lasciva (Meunier, 1907) and P. lepida (Meunier, 1907). Published online in 2024, but the issue date is listed as December 2023.
Ševčík (2024) compares the holotype of Burmacrocera petiolata with macrocerine keroplatid specimens from the Cretaceous amber from Myanmar, and notes the difficulty of attempts to associate similar macrocerine forms with the holotype of B. petiolata.[45]
The first fossil representative of the subgenus Ristocordyla within the genus Brachypeza reported to date is described from the Eocene Baltic amber by Boudet et al. (2024).[46]
Amaral et al. (2024) describe new larval specimens of Qiyia jurassica from the Jurassic Daohugou Beds (China) and new fossil material of brachyceran larvae the Cretaceous amber from Myanmar, including larvae with morphology combining characters seen in members of the families Xylophagidae and Athericidae, and interpret the studied fossils as indicating that members of the group Stratiomyomorpha were abundant in the Cretaceous fauna and likely occupied the ecological functions which are occupied by extant members of more derived brachyceran groups.[47]
Fossil material of aquatic dipterans, including representatives of the family Chaoboridae which are absent from extant fauna of New Zealand, is described from the Miocene Foulden MaarLagerstätte by Baranov, Haug & Kaulfuss (2024).[48]
A member of the family Mesopsychidae. The type species is "Mesopsyche" dobrokhotovae Novokshonov (1997); genus also includes T. shcherbakovi (Novokshonov, 1997), T. justa (Novokshonov & Sukatsheva, 2001), T. ordinata (Novokshonov & Sukatsheva, 2001), T. tortiva (Novokshonov & Sukatsheva, 2001), T. gentica (Novokshonov & Sukatsheva, 2001), T. tongchuanensis (Hong, 2007), T. incompleta (Bashkuev, 2011), T. jinsuoguanensis (Lian, Cai & Huang, 2021) and T. liaoi (Lian, Cai & Huang, 2021), as well as new species T. orientalis, T. sparsanota and T. hongi.
Mecopteran research
Kaczmarek, Li & Soszyńska (2024) describe the first female specimen of Burmothauma eureka, preserved in a piece of the Cretaceous amber from Myanmar that also includes a mite belonging to the family Bdellidae, rove beetles belonging to the subfamilies Scydmaeninae and Staphylininae and flies belonging to the families Cecidomyiidae and Keroplatidae, and interpret both the morphological similarity of the studied specimen to extant Notiothauma reedi and the ecology of arthropods preserved in the same piece of amber as indicating that Cretaceous eomeropids were likely associated with forest litter environments.[53]
Cadena-Castañeda et al. (2024) interpret the family Pseudogryllotalpidae as a junior synonym of the subtribe within the family Gryllidae and the tribe Sclerogryllini, and interpret Pseudogryllotalpa scalprata, Petilus zhengi and Unidigitus longialatus as synonyms of Pherodactylus micromorphus.[67]
Ferreira et al. (2024) reconstruct the left forewing venation of Picogryllus carentonensis, reporting the presence of the venation pattern compatible with the pattern proposed by Josse et al. (2023)[68] for crickets.[69]
Ferreira et al. (2024) reconstruct the anatomy of the internal parts of the genitalia of a male specimen of Picogryllus carentonensis, and evaluate the tempo and mode of evolution of the family Oecanthidae, arguing that the family dates back to the Upper Jurassic.[70]
While describing structures interpreted as a grasshopper ootheca (egg pod) and eggs from the John Day Formation, Oregon, United States, Lee et al. advocate the use of the ootaxonomic nomenclatural system for description of insect egg fossils. They erect the new ichnofamily Entomoothecichnidae to accommodate the described oothecae fossils, and the new oofamily Entomoolithidae for "fossil eggs of entomological affinities".[58]
A collective group name for fossil conicocephalate larvae of ripiphorids (probably belonging to the subfamily Ripidiinae). Includes new species "R." parabolica and "R." kachinensis from the Cretaceous amber of Myanmar, as well as unnamed species from the Cretaceous ambers from Manitoba (Canada) and Taymyr (Russia).
A rove beetle belonging to the supertribe Pselaphitae, with similarities to members of the tribes Arhytodini and Pselaphini. The type species is S. longiscapus.
A rove beetle belonging to the subfamily Phloeocharinae.
Coleopteran research
A review of the evolutionary history of beetles during the late Paleozoic and Mesozoic is published by Beutel et al. (2024).[161]
A study on the diversity of Late Triassic (Norian) beetles from the Cow Branch and Walnut Cove formations (Virginia and North Carolina, United States) is published by Criscione-Vastano & Grimaldi (2024), who identify the presence of 100 distinct beetle morphotypes.[162]
Zippel et al. (2024) revise the fossil record of archostematan larvae and describe the first archostematan larva from the Eocene Baltic amber.[163]
Haug et al. (2024) describe new fossils of adephagan larvae, including the first finding from the Early Cretaceous Jehol Biota, and interpret the studied fossils as indicative of increase of morphological diversity of adephagan larvae over time, with no recognisable losses found by the authors.[164]
Tello, Libido & Moctezuma (2024) describe new fossil material of Onthophagus pilauco from the Pleistocene strata from the Pilauco Bajo site (Chile), providing new information on the morphology of this beetle, and interpret the studied fossils as indicative of the presence of sexual dimorphism in O. pilauco.[165]
Yamamoto & Newton (2024) report the discovery of the first aleocharine rove beetle (a member of the genus Cypha) from the Eocene Bitterfeld amber (Germany).[166]
The first fossil click beetle and ptilodactylid larvae reported to date are described from the Cretaceous amber from Myanmar by Zippel et al. (2024).[167]
A study on the evolutionary history of the family Belidae, as indicated by molecular data and fossil record, is published by Li et al. (2024), who interpret their findings as indicating that the family originated approximately 138 million years ago in Gondwana, as well as indicating that conifers were most likely ancestral hosts of the studied weevils.[169]
A member of the family Caloblattinidae. The type species is A. gigantenna Vršanský from the Upper Jurassic Karabastau Formation in Kazakhstan; genus also includes A. chochoy Vršanský & Kováčová in Vršanský et al. (2024) from the Turonian Emanra Formation (Khabarovsk Krai, Russia).[173]
A member of Mantodea, the type genus of the new family Auroridae. The type species is A. floris. The generic name is preoccupied by Aurora Ragonot (1887) and Aurora Sollas (1888).
A member of the family Corydiidae belonging to the subfamily Latindiinae. The type species is O. samoodpovedaniesi; genus also includes an unnamed species from the Cretaceous amber from Myanmar. The generic name is preoccupied by Okruhliak Vršanský & Hinkelman in Vršanský et al. (2022). Xia et al. (2024) treat O. samoodpovedaniesi as the second species of the genus named by Vršanský & Hinkelman.[178]
A member of the family Blattulidae. Moved from Ctenoblattina tsaganica Vršanský (1999).
Dictyopteran research
Naugolnykh (2024) reports evidence indicating that wings of the blattoid insect Sogdoblatta from the Triassic Madygen Formation (Kyrgyzstan) had the same venation pattern as plants with the pinnate foliages from the same formation, especially members of the genus Cladophlebis, and interprets this finding as likely evidence of mimicry.[185]
Evidence from the study of extant cockroaches, interpreted as indicating that fossil cockroaches cannot be universally classified on the basis of forewing characters, is presented by Li (2024), who considers the families Blattulidae, Caloblattinidae and Mesoblattinidae to be nomina dubia.[186]
McLoughlin et al. (2024) describe opalized casts of fecal pellets from the Cretaceous Griman Creek Formation, interpreted as the oldest evidence of the presence of termites in Australia reported to date.[187]
A member of Apoidea belonging to the family Temnogynidae. The type species is R. festiva; genus also includes R. elongata and R. prima. Its original generic name Rhabdogyna was preoccupied by Rhabdogyna Millidge (1985), necessitating creation of the replacement name Rhapidogyna.[204]
A Formicinae subfamily ant. moved from Camponotus ullrichi (1960). The holotype forewing was considered to be unidentifiable by Boudinot et al. (2024), who consider the taxon to be invalid.[88]
A study on the diversity dynamics of ants throughout their evolutionary history is published by Jouault et al. (2024), who interpret their findings as indicating that extinction of stem ants was more likely caused by their specialized morphology rather than by competition with crown ants, as well as indicating that the radiation of the flowering plants acted as a buffer against extinction and a driver of diversification in ants.[227]
Taniguchi et al. (2024) study the microstructure and distribution of sensilla from the antennae of Gerontoformica gracilis, and find that G. gracilis already had sensilla used by extant ants for detecting alarm pheromones and for distinguishing nestmates from intruders, and was capable of social chemical communication through pheromones used by modern ants.[228]
A Hemerobiidae brown lacewing. The type species is P. kohlsi. Another new species, P. fenestromaculatus Chen, Gao & Liu (2024) was subsequently described from the Eocene Baltic amber.[270]
A member of the family Dipteromantispidae. The type species is T. zuoae.
Neuropteran research
Buchner et al. (2024) describe new lacewing larvae from the Cretaceous amber from Myanmar, demonstrating the presence of trumpet-shaped elongate empodia in members of the families Nymphidae and Osmylidae, and argue that the empodium evolved only once in Neuroptera as was subsequently lost by several neuropteran lineages.[272]
A probable long-necked antlion larva with dark stripes on its legs possibly representing disruptive coloration is described from the Cretaceous amber from Myanmar by Haug, Haug & Haug (2024).[273]
A berothoid larva representing the first record of either the family Berothidae or the family Rhachiberothidae from the Eocene Rovno amber (Ukraine) reported to date is described by Makarkin & Perkovsky (2024).[274]
A member of the family Mesoraphidiidae. Genus includes new species T. macrostigma.
Raphidiopteran research
Haug et al. (2024) describe a snakefly larva from the Cretaceous amber from Myanmar showing a mixture of characters from different developmental stages of extant and fossil snakeflies, and interpret this finding as indicating that metamorphosis was less pronounced in fossil snakeflies than in extant ones.[278]
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 damsel-dragonfly belonging to the family Selenothemistidae. The type species is Y. zaoyuanensis.
Odonatopteran research
New oviposition lesion types, interpreted as evidence of presence of odonatans in Early Jurassic riparian ecosystems of northern Iran, are reported from cycadophyte leaves from the Shemshak Formation by Hashemi, Sadeghi & Wappler (2024).[303]
An aktassiid dragonfly of undetermined generic and specific placement, representing the youngest record of the family reported to date, is described from the Cenomanian amber from Myanmar by Fan et al. (2024).[304]
A member of the family Miridae belonging to the subfamily Psallopinae. The type species is C. uebruum; genus also includes "Isometopsallops" prokopi Vernoux, Garrouste & Nel (2010) from the Lowermost Eocene French amber.
A scale insect belonging to the group Orthezioidea/Paleococcoidea/Archaeococcidea; the type genus of the new family Jankotejacoccidae. The type species is J. libanogloria.
Souma et al. (2024) describe fossil material of Urochelacf.melaina from the Miocene strata from Sado Island (Japan), providing evidence of past distribution of Urochela quadrinotata species group in East Asia and its origin before the Early Miocene.[360]
A review of the forewing venation in the Paleozoic and Mesozoic planthoppers is published by Bucher et al. (2024) [361]
Fabrikant et al. (2024) describe two new specimens of Mimaeurypterus burmiticus from the Cretaceous amber from Myanmar, providing new information on the morphology of this planthopper, and interpret M. burmiticus as adapted to camouflage on tree bark.[362]
A redescription of Bolbossus bervoetsi, based on a female and fifth instar nymph from the Eocene Baltic amber, is published by Gnezdilov (2024).[363]
A study on the evolution of flight performance of members of the family Palaeontinidae is published by Xu et al. (2024), who report that faunal turnover of palaeontinids at the Jurassic-Cretaceous transition was accompanied by improvement in flight abilities, and interpret this change as possibly influenced by the rise of early birds.[364]
Nascimento, Valezio & Krause (2024) describe trace fossils attributed to feeding chambers of cicada nymphs from the Maastrichtian Marília Formation (Brazil), providing evidence of xylem-feeding behavior similar to the behavior of extant cicada nymphs.[365]
Cui et al. (2024) describe new fossil material of Aristovia daniili from the Cretaceous amber from Myanmar, and identify Aristovia as a member of the stem group of Grylloblattodea.[389]
General research
Evidence of the presence of distinct damage patterns on seeds from the Permian (Asselian) Shanxi Formation (China), interpreted as produced by insects with well-developed ovipositors (possibly members of Palaeodictyopteroidea), is presented by Santos, Wappler & (2024).[390]
A study on the taxonomy and taphonomy of insects fossils from Alderton Hill (Gloucestershire, United Kingdom), providing evidence of the presence of a diverse insect fauna (including representatives of 12 orders, 21 families, 24 genera and 21 species) during the Toarcian Oceanic Anoxic Event, is published by Swaby et al. (2024).[391]
A study on mine damage on gymnosperm specimens from the Middle Jurassic Jiulongshan Formation (China), probably produced by members of basal lineages of polyphagan beetles, monotrysian moths and tenthredinoid sawflies, is published by Xiao et al. (2024), who argue that the evolution of the mining associations of insects with gymnospermous plants during the Jurassic was likely caused by the appearance of new, more foliose plant lineages that provided more accessible food resources for mining insects.[392]
A study on the ecology of the Aptian insect fauna from the Nova Olinda Member of the Crato Formation (Brazil) is published by Bezerra & Mendes (2024), who interpret the studied insect fauna as living in an environment similar to modern long-standing wetlands, dominated by dominanted by fully terrestrial taxa, and relatively richer in palaeopterans than insect faunas from the Yixian and Zaza formations.[393]
Storari et al. (2024) compare the preservation of mayfly and orthopteran fossils from the Crato Formation and mayfly fossils from the Upper Jurassic Solnhofen limestones (Germany), interpreting the differences of the preservation of the studied fossils as indicative of the presence of microbial mats during the fossilization of insects from the Crato Formation.[394]
Evidence indicating that the radiation of the flowering plants mitigated insect extinction (especially during the Cretaceous period) and drove the origination of insects (especially during the Cenozoic) is presented by Peris & Condamine (2024).[395]
Loewen et al. (2024) describe a diverse amber deposit from the Maastrichtian strata from the Big Muddy Badlands (Canada), preserving fossils of representatives of seven arthropod orders and at least 11 insect families, and interpret the studied assemblage as providing evidence of a faunal turnover among insects prior to the Cretaceous–Paleogene extinction event.[396]
Eight insect specimens (members of Apocrita and Brachycera, members of the families Libellulidae, Pentatomidae and Bibionidae, and three indeterminate insects), representing the first insect fossils from Serbia reported to date, are described from the Miocene Valjevo-Mionica Basin by Lazarević & Milivojević (2024).[397]
An assemblage of subfossil remains of insects, dominated by diverse beetles, is described from the Late Pleistocene strata from the Lebed site (Altai Republic, Russia) by Gurina et al. (2024), who interpret the studied insects as indicative of humid climate which was significantly colder than modern climate in the studied area.[398]
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^ abHart, L. J.; Ślipiński, A.; Frese, M.; Djokic, T.; McCurry, M. R. (2024). "The first fossil longhorn beetles (Coleoptera: Cerambycidae) from Australia". The Science of Nature. 112 (1). 2. doi:10.1007/s00114-024-01954-0. PMID39680141.
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^Kaulfuss, U.; Szawaryn, K.; Lee, D.; Ruta, R. (2024). "The first beetle species described from Oligocene New Zealand amber (Coleoptera: Scirtidae)". Palaeoentomology. 7 (4): 529–538. doi:10.11646/palaeoentomology.7.4.12.
^Molino-Olmedo, F. (2024). "Description of Cretoctesis conchimillanae gen. et sp. nov. Larva from Burmese Amber (Coleoptera: Buprestidae)". Paleontological Journal. 57 (3 supplement): S262 –S267. doi:10.1134/S0031030123600063.
^ abcLi, Y.-D.; Engel, M. S.; Huang, D.-Y.; Cai, C.-Y. (2024). "Three new species of the extant genus Eucinetus from mid-Cretaceous amber of northern Myanmar (Coleoptera: Eucinetidae)". Zootaxa. 5492 (2): 214–230. doi:10.11646/zootaxa.5492.2.4. PMID39646786.
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^ abEngel, M. S.; Jouault, C. (2024). "Hodotermopsid termites from the mid-Cretaceous Hkamti and Kachin ambers (Isoptera: Hodotermopsidae)". Palaeoentomology. 7 (1): 80–91. doi:10.11646/palaeoentomology.7.1.5.
^ abXia, S.; Sendi, H.; Zhang, X.; Xiao, C.; Luo, C. (2024). "A new cockroach Maculosala circularis gen. et sp. n. (Blattaria: Corydiidae) from mid-Cretaceous Kachin amber of northern Myanmar". Palaeontographica Abteilung A. 329 (1–2): 9–18. Bibcode:2024PalAA.329....9X. doi:10.1127/pala/2024/0155.
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^ abLi, Y.; Wang, M.; Rasnitsyn, A. P.; Shih, C.; Zhuang, J.; Ren, D. (2024). "Two new species of Ghilarellinae (Hymenoptera, Cephoidea, Sepulcidae) from the Lower Cretaceous". Cretaceous Research. 159. 105875. Bibcode:2024CrRes.15905875L. doi:10.1016/j.cretres.2024.105875.
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^ abcdChemyreva, V. G.; Vasilenko, D. V.; Perkovsky, E. E. (2024). "'Where there are many cattle' in the Eocene of Ukraine: Review of Ambositra Masner (Hymenoptera, Diapriidae, Ambositrinae) from Rovno amber, with the description of three new species". Zootaxa. 5446 (4): 499–516. doi:10.11646/zootaxa.5446.4.3. PMID39645860.
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^Álvarez-Parra, S.; Jouault, C.; Azar, D. (2024). "A braconid wasp (Hymenoptera: Braconidae) with second recurrent vein in forewing from Lower Cretaceous Spanish amber". Palaeoentomology. 7 (4): 479–490. doi:10.11646/palaeoentomology.7.4.7.
^ abBelokobylskij, S. A.; Manukyan, A. R. (2024). "First reliable fossil record of the subfamily Rhysipolinae (Hymenoptera: Braconidae): a new subgenus and species of the genus Rhysipolis Foerster, 1863 from Baltic amber". Zootaxa. 5448 (4): 591–600. doi:10.11646/zootaxa.5448.4.10. PMID39646235.
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^Zhuang, Y.; Li, J.; Jarzembowski, E. A.; Wang, B.; Zhang, Q. (2024). "A new genus of Panguoidea in Lower Cretaceous Wealden amber". Historical Biology: An International Journal of Paleobiology: 1–4. doi:10.1080/08912963.2024.2309637.
^ abWu, Q.; Vilhelmsen, L.; Engel, M. S.; Shih, C.K.; Ren, D.; Gao, T.P. (2024). "Two new species of Burmusculidae (Hymenoptera: Pompiloidea) in mid-Cretaceous amber from northern Myanmar". Palaeoentomology. 7 (2): 284–290. doi:10.11646/palaeoentomology.7.2.12.
^Álvarez-Parra, S.; Engel, M. S.; Peñalver, E.; Azar, D. (2024). "The aculeate wasp family Sierolomorphidae (Hymenoptera) in the Early Cretaceous". Insect Systematics and Diversity. 8 (4). 7. doi:10.1093/isd/ixae020.
^Zhang, Q.; Jia, N.; Li, Y.; Wang, J.; Rasnitsyn, A. P. (2024). "New genus of falsiformicid wasps (Hymenoptera, Vespoidea: Falsiformicidae) with brachypterous male from middle Cretaceous Kachin amber in Myanmar". Cretaceous Research. 168. 106057. doi:10.1016/j.cretres.2024.106057.
^Engel, M. S.; Nguyen, L. T. P; Nel, A. (2024). "A new genus of polistine wasps from the Oligocene of Aix-en-Provence, France (Hymenoptera: Vespidae)". Palaeoentomology. 7 (2): 217–220. doi:10.11646/palaeoentomology.7.2.4.
^Li, R.-Y.; Li, H.-Y.; Liu, X.-Y. (2024). "A new genus of beaded lacewings (Neuroptera: Berothidae) from the mid-Cretaceous Myanmar amber". Palaeoentomology. 7 (4): 491–498. doi:10.11646/palaeoentomology.7.4.8.
^ abKhramov, A. V.; Nam, G.-S. (2024). "Discovery of supposedly "Gondwanan" myrmeleontoids (Neuroptera) in the Lower Cretaceous of South Korea". Cretaceous Research. 166. 106024. doi:10.1016/j.cretres.2024.106024.
^Wang, J.; Shi, C.; Liu, X.; Shih, C.; Ren, D.; Wang, Y. (2024). "A new stem-group mantispoid lineage (Insecta: Neuroptera) equipped with unique raptorial structures from the Middle Jurassic of China". Journal of Systematics and Evolution. doi:10.1111/jse.13125.
^Makarkin, V. N.; Perkovsky, E. E. (2024). "Nothochrysinae (Neuroptera: Chrysopidae) from the early Eocene Fur Formation, Denmark, with description of a new genus". Zootaxa. 5433 (3): 529–545. doi:10.11646/zootaxa.5433.4.3. PMID39646756.
^ abBoderau, M.; Ngo-Muller, V.; Nel, A. (2024). "First representatives of the stonefly genus Perlomyia and the beaded lacewing genus Isoscelipteron from the Upper Miocene of France (Plecoptera: Leuctridae and Neuroptera: Berothidae), with biogeographical considerations". Zootaxa. 5481 (1): 131–140. doi:10.11646/zootaxa.5481.1.8. PMID39646049.
^ abChen, C.; Peng, Z.; Shi, C.; Ren, D.; Yang, Q. (2024). "New findings of dipteromantispids (Insecta: Neuroptera) from Upper Cretaceous Myanmar amber". The Anatomical Record. 307 (10): 3274–3281. doi:10.1002/ar.25435. PMID38567519.
^ abMakarkin, V. N. (2024). "First brown lacewings (Neuroptera: Hemerobiidae) from the early Eocene Green River Formation". Zootaxa. 5501 (1): 160–170. doi:10.11646/zootaxa.5501.1.7. PMID39647121.
^ abChen, Z.-L.; Zhuo, D.; Xu, C.-P.; Liu, X.-Y. (2024). "Discovery of new brown lacewings from the mid-Cretaceous Kachin amber highlights the Cretaceous diversity of Hemerobiidae (Insecta: Neuroptera)". Palaeoentomology. 7 (5): 659–674. doi:10.11646/palaeoentomology.7.5.9.
^ abLi, Z.; Zhuo, D.; Gao, Y.; Xu, C.; Zhang, W.; Wang, Y.; Liu, X. (2024). "A review of the lance lacewings (Neuroptera: Osmylidae) from the mid-Cretaceous amber of Myanmar". Cretaceous Research. 160. 105895. Bibcode:2024CrRes.16005895L. doi:10.1016/j.cretres.2024.105895.
^Kong, B.; Shih, C.; Ren, D.; Wang, Y. (2024). "A new giant Jurassic lacewing larva reveals a particular aquatic habit and its significance to the palaeoecology". Journal of Systematics and Evolution. 62 (6): 1193–1200. doi:10.1111/jse.13071.
^Hart, L. J.; Engel, M. S.; Frese, M.; McCurry, M. R. (2024). "The first fossil mantis lacewing (Neuroptera: Mantispidae) from Australia". Palaeoentomology. 7 (3): 345–348. doi:10.11646/palaeoentomology.7.3.3.
^Makarkin, V. N.; Wedmann, S. (2024). "A new species of Hemerobiidae (Neuroptera) from the late Eocene Rovno amber". Zootaxa. 5538 (6): 595–600. doi:10.11646/zootaxa.5538.6.6. PMID39645678.
^Chen, Z.-L.; Gao, Y.-H.; Liu, X.-Y. (2024). "A new brown lacewing species of the genus Pseudonotherobius Makarkin, 2024 (Neuroptera: Hemerobiidae) from the Eocene Baltic amber". Palaeoentomology. 7 (6): 746–752. doi:10.11646/palaeoentomology.7.6.10.
^ abLambkin, K. J. (2024). "Fossil insects of the Middle Triassic Gayndah Formation of south-eastern Queensland". Memoirs of the Queensland Museum – Nature. 65: 30–46. doi:10.17082/j.2204-1478.65.2024.2024-02.
^Haug, C.; Haug, G. T.; Haug, J. T. (2024). "The first record of disruptive colouration in holometabolan larvae from about 100 million-year-old Kachin amber is a lacewing larva with dark stripes on the legs". Palaeoentomology. 7 (6): 719–722. doi:10.11646/palaeoentomology.7.6.7.
^Makarkin, V. N.; Perkovsky, E. E. (2024). "A remarkable fossil berothoid larva (Neuroptera) from the late Eocene Rovno amber (Ukraine)". Historical Biology: An International Journal of Paleobiology: 1–9. doi:10.1080/08912963.2023.2297909.
^ abLu, X.; Stubbs, T. L.; Zhuo, D.; Xu, C.; Donoghue, P. C. J.; Liu, X. (2024). "New Cretaceous snakeflies highlight the morphological disparity of Mesoraphidiidae and its response to the Cretaceous Terrestrial Revolution". Insect Systematics and Diversity. 8 (4). 8. doi:10.1093/isd/ixae016.
^Chen, Y.; Jarzembowski, E. A.; Chen, L.; Luo, C. (2024). "Laiyangoraphidia delicata gen. et sp. nov., a new snakefly (Insecta: Raphidioptera: Mesoraphidiidae) from the Lower Cretaceous Laiyang Formation of China". Historical Biology: An International Journal of Paleobiology: 1–6. doi:10.1080/08912963.2024.2384588.
^Chen, Y.; Jarzembowski, E. A.; Chen, L.; Luo, C. (2024). "A new species of Proraphidia (Raphidioptera: Mesoraphidiidae) from the Lower Cretaceous Laiyang Formation of China". Cretaceous Research. 160. 105898. Bibcode:2024CrRes.16005898C. doi:10.1016/j.cretres.2024.105898.
^ abNel, A.; Oudoire, T.; Garrouste, R. (2024). "New taxa in ancient collections: the Carboniferous Palaeodictyoptera (Insecta) from the Natural History Museum of Lille (France)". Palaeoentomology. 7 (5): 675–683. doi:10.11646/palaeoentomology.7.5.10.
^Rosová, K.; Heising, M.; Leipner, A.; Prokop, J. (2024). "A new palaeodictyopteran Haseneura jarmilae gen. et sp. nov. from the Pennsylvanian of Piesberg reveals the structure of alinota". Historical Biology: An International Journal of Paleobiology: 1–8. doi:10.1080/08912963.2024.2407499.
^ abcMueller, A. S.; Demers-Potvin, A. V. (2024). "New Late Cretaceous (Cenomanian) fossil mayfly nymphs (Oligoneuriidae, Heptageniidae, Hexagenitidae) from the Redmond Formation, Labrador, Canada". Canadian Journal of Earth Sciences. 61 (6): 712–722. Bibcode:2024CaJES..61..712M. doi:10.1139/cjes-2023-0133.
^Chen, Z.-T.; Zheng, X. (2024). "Crephlebia gen. nov., a new mayfly genus (Ephemeroptera: Leptophlebiidae) from mid-Cretaceous Kachin amber of northern Myanmar". Cretaceous Research. 159. 105869. Bibcode:2024CrRes.15905869C. doi:10.1016/j.cretres.2024.105869.
^Sroka, P.; Prokop, J. (2024). "The oldest Australian mayfly (Insecta, Ephemerida) from the Middle Triassic at Brookvale, New South Wales". Alcheringa: An Australasian Journal of Palaeontology. 48 (2): 313–318. Bibcode:2024Alch...48..313S. doi:10.1080/03115518.2024.2346587.
^Nel, A.; Huang, D.-Y.; Lian, X.-N. (2024). "Redescription of the 'libelluloid' Mesocordulia boreala (Odonata: Mesocorduliidae) from the Lower Cretaceous of China". Zootaxa. 5562 (1): 31–37. doi:10.11646/zootaxa.5562.1.6.
^ abNel, A. (2024). "Two new damselflies from the Eocene Green River Formation (Odonata, Zygoptera, Dysagrionidae, Thaumatoneuridae)". Zootaxa. 5446 (4): 588–594. doi:10.11646/zootaxa.5446.4.11. PMID39645852.
^Liu, Y.X.; Chen, P.C.; Shi, C.F.; Ren, D.; Yang, Q. (2024). "The oldest aktassiid dragonfly (Odonata: Petaluroidea) from the Middle Jurassic of China". Palaeoentomology. 7 (2): 237–244. doi:10.11646/palaeoentomology.7.2.7.
^ abcdefghijklFelker, A. S. (2024). "New Taxa of Damselflies (Protozygoptera) from the Permian of the East European Platform". Paleontological Journal. 57 (8): 857–914. doi:10.1134/S0031030123080038.
^Liu, P.; Nel, A.; Zhuo, D.; Zheng, D. (2024). "A new burmagomphid dragonfly (Odonata, Anisoptera, Gomphides) from mid-Cretaceous Kachin amber". Palaeontographica Abteilung A. 329 (1–2): 1–8. Bibcode:2024PalAA.329....1L. doi:10.1127/pala/2024/0154.
^Azar, D.; Maksoud, S.; Abi-Saad, P.; Nel, A. (2024). "A new, to date endemic, family of dragonfly in the mid-Cretaceous fossil fish Konservat-Lagerstätte of Haqel, Lebanon (Odonata: Anisoptera)". Zootaxa. 5497 (1): 142–160. doi:10.11646/zootaxa.5497.1.9. PMID39647158.
^Liu, P.; Fang, R.; Zheng, D. (2024). "A new burmaeshnid dragonfly (Odonata, Anisoptera, Aeshnoptera) from mid-Cretaceous Kachin amber, north Myanmar". Zootaxa. 5538 (1): 74–78. doi:10.11646/zootaxa.5538.1.7. PMID39645719.
^Qi, P.; Liu, P.; Xiao, C.; Zheng, D. (2024). "A new hemeroscopid dragonfly (Odonata, Anisoptera) from the Lower Cretaceous of the Jiuquan Basin, northwestern China". Zootaxa. 5432 (4): 567–572. doi:10.11646/zootaxa.5432.4.6. PMID39645768.
^ abNel, A.; Xu, M.; Wang, Y.; Song, X.; Gao, J.; Ji, G.; Huang, D. (2024). "New Chinese Jurassic damsel-dragonflies of the families Paragonophlebiidae, Selenothemistidae and Isophlebiidae (Odonata, Epiproctophora) from the Jurassic Ordos Basin of NW China". Geobios. 87: 37–44. Bibcode:2024Geobi..87...37N. doi:10.1016/j.geobios.2024.08.014.
^Simonsen, T. J.; Archibald, S. B.; Rasmussen, J. A.; Sylvestersen, R. L.; Olsen, K.; Ware, J. L. (2024). "Stolleagrion foghnielseni (Odonata, Cephalozygoptera, Dysagrionidae) gen. et sp. nov.: a new odonatan from the PETM recovery phase of the earliest Ypresian Fur Formation, Denmark". Zootaxa. 5415 (3): 493–498. doi:10.11646/zootaxa.5415.3.9. PMID38480188.
^ abChen, J.; Zhuo, D.; Wang, W.; Zheng, Y.; An, B. (2024). "New Sinoalidae (Hemiptera, Cercopoidea) in Cenomanian Kachin amber, with notes on its paleobiogeographic implications". Cretaceous Research. 159. 105876. Bibcode:2024CrRes.15905876C. doi:10.1016/j.cretres.2024.105876.
^Dietrich, C. H.; Wang, M.-L. (2024). "A new genus and species representing the first Mesozoic eurymeline leafhopper (Hemiptera: Cicadellidae: Eurymelinae: Macropsini)". Palaeoentomology. 7 (4): 507–512. doi:10.11646/palaeoentomology.7.4.10.
^Zhang, F.; Bourgoin, T.; Song, Z.; Chen, R.; Xiao, C.; Luo, C. (2024). "Imbricatala novitas gen. et sp. nov., a new planthopper of family Inoderbidae (Hemiptera: Fulgoromorpha: Fulgoridioidea) from mid-Cretaceous Kachin amber of northern Myanmar". Palaeontographica Abteilung A. 328 (1–6): 123–134. doi:10.1127/pala/2024/0151.
^ abcdBoderau, M.; Garrouste, R.; Nel, A. (2024). "The Middle Permian of southern France and a new protopsyllidioidean family reveals a shared hemipteran fauna with the Permian of the Russian Federation". Alcheringa: An Australasian Journal of Palaeontology: 1–11. doi:10.1080/03115518.2024.2392493.
^Azar, D.; Maksoud, S.; Robin, N.; Godefroit, P.; Cavin, L.; Olive, S.; Rey, K.; Vallée-Gillette, N.; De Brito, L.; Heneine, G.; Nel, A. (2024). "The first and oldest record of Issidae from the Lower Cretaceous of Lebanon (Hemiptera, Fulgoromorpha)". Zootaxa. 5562 (1): 38–44. doi:10.11646/zootaxa.5562.1.7.
^Jouault, C.; Nam, G.-S.; Boderau, M.; Kwon, S.-H.; Engel, M. S. (2024). "A new Triassic Tettigarctidae (Insecta, Hemiptera) from the Amisan Formation (Republic of Korea)". Palaeoentomology. 7 (1): 132–140. doi:10.11646/palaeoentomology.7.1.9.
^Hakim, M.; Fu, Y.-Z. (2024). "A new record of Scytinopteridae from the Middle Triassic Tongchuan entomofauna of China". Journal of Insect Biodiversity. 60 (1): 55–63. doi:10.12976/jib/2024.60.1.9.
^Zhang, Q.-Q.; Li, L.; Szwedo, J.; Bao, T.; Zhang, H.-C. (2024). "A new fulgoroidian insect (Hemiptera: Surijokocixiidae) from the Middle Triassic Tongchuan Formation of northwestern China". Palaeoworld. 33 (6): 1620–1625. Bibcode:2024Palae..33.1620Z. doi:10.1016/j.palwor.2024.02.001.
^Fu, Y.-Z.; Nel, A.; Boderau, M. (2024). "A new early representative genus of Hylicellidae from the Triassic of China (Hemiptera, Cicadomorpha)". Journal of Insect Biodiversity. 60 (1): 9–15. doi:10.12976/jib/2024.60.1.4 (inactive 1 January 2025).{{cite journal}}: CS1 maint: DOI inactive as of January 2025 (link)
^Zhang, Q.; Chen, J.; Wang, Y.; Zhang, L.; Zhang, H. (2024). "A new procercopid froghopper (Hemiptera: Cicadomorpha: Procercopidae) from the Lower Cretaceous Jiufotang Formation, western Liaoning Province, NE China". Historical Biology: An International Journal of Paleobiology. doi:10.1080/08912963.2024.2403594 (inactive 1 November 2024).{{cite journal}}: CS1 maint: DOI inactive as of November 2024 (link)
^Boderau, M.; Nel, A. (2024). "The second treehopper species in Miocene Dominican amber (Hemiptera: Membracidae)". Annales de la Société Entomologique de France. Nouvelle Série. 60 (1): 48–52. doi:10.1080/00379271.2024.2305404.
^Fabrikant, D.; Huang, D.-Y.; Nel, A.; Fu, Y.-Z. (2024). "New Cicadomorpha from the Triassic of China raise questions on the systematics of Archijassidae". Journal of Insect Biodiversity. 60 (1): 75–82. doi:10.12976/jib/2024.60.1.11.
^Allsopp, P. G. (2024). "Vulcanetoia, a new replacement name for the genus Vulcanoia Martins-Neto, 1988 (Insecta: Hemiptera: Lalacidae: Lalacinae: Carpopodini)". Zootaxa. 5403 (2): 295–296. doi:10.11646/zootaxa.5403.2.9. PMID38480439.
^You, Y.-J.; Jiang, T.; Guan, X.-E.; Bieszczad, B.; Szwedo, J. (2024). "A second progonocimicid (Hemiptera: Coleorrhyncha) from the Middle Cretaceous Kachin amber of Myanmar". Palaeoworld. 200904. doi:10.1016/j.palwor.2024.200904.
^Zhang, P.P.; Liu, Y.Q.; Ren, D.; Yao, Y.Z. (2024). "The first report of fossil of Centrocnemidinae (Hemiptera: Heteroptera: Reduviidae) in the Mesozoic". Palaeoentomology. 7 (2): 314–323. doi:10.11646/palaeoentomology.7.2.16.
^Ma, Y.; Du, S.; Ren, D.; Yao, Y. (2024). "A new species of Nabidae (Hemiptera, Heteroptera, Cimicomorpha) from Dominican amber". Historical Biology: An International Journal of Paleobiology: 1–6. doi:10.1080/08912963.2024.2383705.
^Zhang, X.-Y.; Ren, D.; Yao, Y.-Z. (2024). "The first sphagnum bug (Hemiptera: Hebridae) from the Late Cretaceous Kachin amber". Palaeoentomology. 7 (3): 407–413. doi:10.11646/palaeoentomology.7.3.10.
^ abJarzembowski, E. A.; Wang, B. (2024). "Early Cretaceous nepomorph bugs from the Wealden of the Weald". Palaeoentomology. 7 (3): 349–352. doi:10.11646/palaeoentomology.7.3.4.
^Boderau, M.; Ngô-Muller, V.; Garrouste, R.; Nel, A. (2024). "The second genus of pond treaders (Heteroptera: Mesoveliidae) from mid-Cretaceous amber of Myanmar". Annales de Paléontologie. 110 (3). 102685. Bibcode:2024AnPal.11002685B. doi:10.1016/j.annpal.2024.102685.
^Bush, T.; Berenger, J.-M.; Gil-Santana, H.; Forthman, M.; Hoey-Chamberlain, R.; Weirauch, C. (2024). "Systematics of Ectrichodiella Fracker and Bruner, 1924, with description of the first fossil millipede assassin bug species (Insecta: Hemiptera: Reduviidae: Ectrichodiinae)". American Museum Novitates (4025): 1–40. doi:10.1206/4025.1. hdl:2246/7378.
^Cumming, R. T.; Le Tirant, S.; Chen, H. (2024). "An additional Cretaceous Ferriantenna Cumming & Le Tirant, 2021 species with wildly exaggerated antennae (Hemiptera, Coreidae)". Faunitaxys. 12 (5): 1–6. doi:10.57800/faunitaxys-12(5).
^Sohn, J.-C.; Nam, G. S. (2024). "New fossil genus and species of Yuripopovinidae (Insecta: Heteroptera, Coreoidea) from the Lower Cretaceous Jinju Formation, South Korea, with insights into the evolution of exaggerated antennae in the family". Cretaceous Research. 158. 105847. Bibcode:2024CrRes.15805847S. doi:10.1016/j.cretres.2024.105847.
^Chen, J.; Zhuo, D. (2024). "A new remarkable big-eyed minute litter bug in Cenomanian Kachin amber from Myanmar (Hemiptera, Dipsocoromorpha)". Cretaceous Research. 161. 105919. Bibcode:2024CrRes.16105919C. doi:10.1016/j.cretres.2024.105919.
^Boderau, M.; Nel, A.; Maksoud, S.; Abi-Saad, P.; Azar, D. (2024). "The first aquatic insect fossil from the Cenomanian Konservat-Lagerstätte of Haqel (Lebanon) fills a gap in the fossil record of giant water bugs (Heteroptera: Belostomatidae)". Zootaxa. 5562 (1): 11–22. doi:10.11646/zootaxa.5562.1.4.
^Ma, Y.N.; Du, S.L.; Ren, D.; Yao, Y.Z. (2024). "A new genus and species of Nabinae (Heteroptera: Cimicomorpha: Nabidae) from mid-Cretaceous Burmese amber". Palaeoentomology. 7 (2): 306–313. doi:10.11646/palaeoentomology.7.2.15.
^Boderau, M.; Ngô-Muller, V.; Peng, A.C.; Engel, M. S.; Garrouste, R.; Nel, A. (2024). "Phimophorus chiodii sp. nov., first representative of a cryptic assassin bug subfamily from Dominican amber (Reduviidae: Phimophorinae) as revealed with traditional light microscopy and computed micro-tomographic reconstruction". Palaeoentomology. 7 (2): 299–305. doi:10.11646/palaeoentomology.7.2.14.
^Chen, J.; Zhuo, D.; Ren, G.; Yang, F.; An, B. (2024). "A beetle-like minute litter bug trapped in 99 million-year-old Kachin amber (Hemiptera, Dipsocoromorpha, Schizopteridae)". Cretaceous Research. 167. 106034. doi:10.1016/j.cretres.2024.106034.
^Mu, C.-M.; Wang, Y.-X.; Ren, D.; Yao, Y.-Z. (2024). "A new species of genus Tingiometra from mid-Cretaceous Kachin amber (Heteroptera: Tingidae: Tingiometrinae)". Palaeoentomology. 7 (6): 703–706. doi:10.11646/palaeoentomology.7.6.3.
^Dai, R.; Du, S.L.; Hu, Z.K.; Ren, D.; Yao, Y.Z. (2024). "New genus and species of Yuripopovinidae (Heteroptera: Pentatomomorpha) from mid-Cretaceous Burmese amber". Palaeoentomology. 7 (2): 291–298. doi:10.11646/palaeoentomology.7.2.13.
^ abcdBurckhardt, D.; Drohojowska, J.; Štarhová Serbina, L.; Malenovský, I. (2024). "First record of jumping plant lice of the family Liviidae (Hemiptera, Sternorrhyncha, Psylloidea) from Dominican amber". Neues Jahrbuch für Geologie und Paläontologie - Abhandlungen. 311 (2): 215–227. doi:10.1127/njgpa/2024/1195.
^Drohojowska, J.; Bogusiak, W.; Kurkina, S.; Szwedo, J. (2024). "A third aleurodicine from the Eocene Baltic amber – Eogroehnia carsteni nov. gen., nov. sp. (Hemiptera, Sternorrhyncha, Aleyrodidae)". Geobios. doi:10.1016/j.geobios.2024.08.008.
^Hakim, M.; Huang, D.-Y. (2024). "A puzzling Cretaceous psyllid-type forewing from the South of China". Zootaxa. 5562 (1): 23–30. doi:10.11646/zootaxa.5562.1.5.
^Drohojowska, J.; Evans, G. A.; Kaulfuss, U.; Lee, D. E.; Szwedo, J. (2024). "First Miocene whiteflies and psyllids (Hemiptera: Sternorrhyncha: Aleyrodoidea and Psylloidea) from Aotearoa New Zealand". Palaeobiodiversity and Palaeoenvironments. Bibcode:2024PdPe..tmp...51D. doi:10.1007/s12549-024-00628-z.{{cite journal}}: CS1 maint: bibcode (link)
^Ivanov, G. A.; Vorontsov, D. D.; Shcherbakov, D. E. (2024). "A remarkable psyllomorph family from Cretaceous Burmese amber, Miralidae stat. nov. (= Dinglidae syn. nov.; Hemiptera: Sternorrhyncha)". Cretaceous Research. 106069. doi:10.1016/j.cretres.2024.106069.
^Rédei, D. (2024). "A re-assessment of Palaeotanyrhina (Hemiptera: Heteroptera) elucidates the phylogeny of Leptopodoidea". Insect Systematics and Diversity. 8 (6). 5. doi:10.1093/isd/ixae030.
^Souma, J.; Takahashi, Y.; Aiba, H.; Aida, M. (2024). "Discovery of the fossil true bug species Urochela (Urochela) cf. melaina Zhang, 1989 (Hemiptera: Heteroptera: Urostylididae) from Japan, suggesting a wide distribution of the U. (U.) quadrinotata (Reuter, 1881) species group in East Asia in the past". Zootaxa. 5507 (4): 589–596. doi:10.11646/zootaxa.5507.4.6. PMID39646604.
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