Palaeoentomology
https://www.mapress.com/pe
<p><strong>Palaeoentomology </strong>is the official journal of the <a href="http://fossilinsects.net/">International Palaeoentomological Society</a> (IPS). It is an international peer-reviewed scientific journal, which publishes high quality, original research contributions as well as review papers. Papers are published in English and they cover a wide spectrum of topics in palaeoentomology, fossil terrestrial arthropods and amber research, i.e. systematic palaeontology, morphology, diversity, palaeogeography, palaeoecology, palaeobehavior, evolutionary and phylogenetic studies on fossil insects and terrestrial arthropods, biostratigraphy, taphonomy, and amber (deposits, inclusions, geochemistry, curation). Descriptions of new methods (analytical, instrumental or numerical) should be relevant to the broad scope of the journal.</p> <p> </p> <p>Palaeoentomology is the flag journal of IPS, who is responsible for the editing of this journal. For more info about IPS, please contact Prof. Dr. Hab. Dany Azar, Lebanese University, Lebanon. danyazar@ul.edu.lb</p>Magnolia pressen-USPalaeoentomology2624-2826<span lang="EN-GB">Authors need to complete and return an </span><span lang="EN-GB"><a href="/phytotaxa/images/copyright.rtf">Assignment of Copyright</a> </span><span lang="EN-GB">form when a paper is accepted for publication. Authors from institutions that do not allow transfer of copyrights to publishers (e.g. government institutions such as USDA, CSIRO) should attach a copyright waiver or similar document.</span><strong>Earwigs from the late Oligocene crater lake of Enspel, Germany (Dermaptera)</strong>
https://www.mapress.com/pe/article/view/palaeoentomology.8.4.4
<p lang="en-US" align="justify"><span style="color: #000000;"><span style="font-family: Times New Roman, serif;"><span style="font-size: small;"><span style="color: #000002;">The Konservat-Lagerstätte of Enspel, Germany preserves </span><span style="color: #000002;">an exceptional late Oligocene biota, with abundant remains </span><span style="color: #000002;">of insects. Here we provide the first formal descriptions of earwigs from the crater lake of Enspel, all adults and comprising two distinct species. </span><span style="color: #000002;"><em>Kraterlabis primordialis</em></span> <span style="color: #000002;"><strong>gen. et sp. nov.</strong></span><span style="color: #000002;"> is a possible anisolabidid and is a wholly apterous, including complete absence of tegmina, and is distinguished by the form of the thoracic nota and the </span><span style="color: #000002;">distinctive pygidium and cercal forceps. The holotype</span><span style="color: #000002;"> of </span><span style="color: #000002;"><em>Adiathetodes nassauensis</em></span> <span style="color: #000002;"><strong>gen. et sp. nov.</strong></span><span style="color: #000002;">, unlike </span><span style="color: #000002;"><em>K. primordialis</em></span><span style="color: #000002;">, is heavily pyritized but with lots of character </span><span style="color: #000002;">information discernible. The species is likely a chelisochid as indicated by the form of the second tarsomere that projects</span> <span style="color: #000002;">strongly ventral to the third and with the third nearly as long as the first tarsomere. The genus is distinguished in the form</span><span style="color: #000002;"> of the pygidium and cercal forceps, as well as the thorax. </span></span></span></span></p>MICHAEL S. ENGELMARKUS J. POSCHMANNTORSTEN WAPPLERANDRÉ NELANCHENG PENG
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2025-08-292025-08-298436336910.11646/palaeoentomology.8.4.4<strong>New taxa and wing venation disparity in Vitimotauliidae (Trichoptera) from the Lower Cretaceous Yixian Formation</strong>
https://www.mapress.com/pe/article/view/palaeoentomology.8.4.5
<p lang="en-US" align="justify"><span style="color: #000000;"><span style="font-family: Times New Roman, serif;"><span style="font-size: small;">Vitimotauliidae, an extinct caddisfly family with the highest Mesozoic palaeobiodiversity, remains poorly represented in China, with only a few species. Herein, based on comparative morphology and geometric morphometric analyses, one new genus, <em>Trichosukatshevia</em> <strong>gen. nov.</strong>, with two new species, <em>T</em>.<em> simplex </em><strong>sp. nov.</strong> and <em>T</em>. <em>furcivenata </em><strong>sp. nov.</strong>, and one new species of <em>Multimodus</em> Sukatsheva, 1968, <em>M</em>.<em> yixianensis </em><strong>sp. nov.</strong> are described and illustrated from the Lower Cretaceous of Yixian Formation in China. These discoveries of new taxa significantly enhance the taxonomic diversity of Vitimotauliidae. Notably, among them, <em>Trichosukatshevia</em> <strong>gen. nov.</strong> represents a novel lineage characterized by an open MC, a previously unreported character in the family. Moreover, morphological variations at the branching point of F4 and cross-vein m-cua are identified, expands the known morphological disparity of wing venation in Vitimotauliidae. This study highlights the evolutionary and morphological complexity of Mesozoic caddisflies, providing critical insights into their diversification during the Early Cretaceous.</span></span></span></p>JIA-WEI CHAOCHUNG-KUN SHIHXI-SEN JIADONG RENJIA-JIA WANG
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2025-08-292025-08-298437038410.11646/palaeoentomology.8.4.5<strong>Calyptrate flies in fossil resin from Mexico and Tanzania</strong>
https://www.mapress.com/pe/article/view/palaeoentomology.8.4.6
<p lang="en-US" align="justify"><span style="color: #000000;"><span style="font-family: Times New Roman, serif;"><span style="font-size: small;">Fossil Calyptratae flies are exclusively found in the Cenozoic. Calyptrates arose around the K-T boundary and rapidly diversified in the early Tertiary. Only a few species of fossil Calyptratae are known from fossil resins such as Baltic amber, Dominican amber, and East African copal or Defaunation resin. However, these preserved organisms provide valuable insights into the evolutionary and ecological history of calyptrate flies. In this study, we describe <em>Mesembrinella</em> <em>guimaraesi</em><strong> sp. nov.</strong> (Mesembrinellidae) from Miocene Mexican amber, representing the first record of a calyptrate from this fossiliferous site; and we report <em>Dichaetomyia immaculiventris </em>Malloch as the first occurrence of <em>Dichaetomyia</em> Malloch (Muscidae) in Tanzanian copal. We also briefly discuss the abundance of calyptrate flies in resins and actualistic experiments.</span></span></span></p>LUCAS R. P. GOMESMÓNICA M. SOLÓRZANO-KRAEMER
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2025-08-292025-08-298438539410.11646/palaeoentomology.8.4.6<strong>The first fossil species of <em>Hermetia</em> Latreille, 1804 (Diptera: Stratiomyidae) in Miocene Mexican amber</strong>
https://www.mapress.com/pe/article/view/palaeoentomology.8.4.7
<p lang="en-US" align="justify"><span style="color: #000000;"><span style="font-family: Times New Roman, serif;"><span style="font-size: small;"><span style="color: #010003;">The first fossil species of </span><span style="color: #010003;"><em>Hermetia</em></span><span style="color: #010003;"> Latreille, 1804 (Diptera: Stratiomyidae) is described as </span><span style="color: #010003;"><em>Hermetia cenoteevani</em></span> <span style="color: #010003;"><strong>sp. nov.</strong></span><span style="color: #010003;">, based on a female specimen preserved in Miocene Mexican amber. This new </span><span style="color: #010003;"><em>Hermetia</em></span><span style="color: #010003;"> species shares with the </span><span style="color: #010003;">extant species </span><span style="color: #010003;"><em>Hermetia flavipes </em></span><span style="color: #010003;">Wiedemann, 1830 and with </span><span style="color: #010003;"><em>Hermetia teevani</em></span><span style="color: #010003;"> Curran, 1934 a short and slender body shape, </span><span style="color: #010003;">bare eyes, and the presence of a subtle beak-like projection in</span><span style="color: #010003;"> the face. </span><span style="color: #010003;"><em>Hermetia cenoteevani</em></span> <span style="color: #010003;"><strong>sp. nov. </strong></span><span style="color: #010003;">is distinguished by a light-colored scutellum on its distal two-thirds and light-colored abdominal tergites with dark transverse bands on tergites 1–5, with no semi-translucent area on tergites 1–2. </span><span style="color: #010003;"><em>Hermetiella bifurcata</em></span><span style="color: #010003;"> Meunier, 1908, the only other fossil species previously assigned to the Hermetiinae, does not fit within this subfamily or even Stratiomyidae. Therefore, we </span><span style="color: #010003;">place it as </span><span style="color: #010003;"><em>incertae sedis</em></span><span style="color: #010003;"> within the suborder Brachycera.</span></span></span></span></p>DIEGO AGUILAR FACHINLUCAS ROBERTO PEREIRA GOMES
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2025-08-292025-08-298439540110.11646/palaeoentomology.8.4.7<strong>The first water-penny beetle (Coleoptera: Psephenidae) in Baltic amber, with a list of Dryopoidea described from the mid-late Eocene European ambers</strong>
https://www.mapress.com/pe/article/view/palaeoentomology.8.4.8
<p lang="en-US" align="justify"><span style="color: #000000;"><span style="font-family: Times New Roman, serif;"><span style="font-size: small;"><span style="color: #040409;">Based on a well-preserved adult inclusion in Baltic amber, the first extinct species of the subfamily Eubriinae and the </span><span style="color: #040409;">first representative of the family Psephenidae from the Eocene fossil resin is described and illustrated. The new fossil species belonging to the extant genus, </span><span style="color: #040409;"><em>Macroeubria</em></span> <span style="color: #040409;"><em>groehni</em></span><span style="color: #040409;"><strong> sp. nov.</strong></span><span style="color: #040409;">, is compared with related extant taxa. Two additional fossil records of previously described Dryopoidea from Eocene Baltic amber of the Sambian Peninsula deposited in the collection of the Kaliningrad amber museum are provided. A brief updated list of the described Dryopoidea species from Baltic and Rovno ambers is compiled. The currently described diversity of the superfamily in the mid-late Eocene European ambers consists of 11 extinct species belonging to nine genera within five families.</span></span></span></span></p>VITALII ALEKSEEVANDRIS BUKEJS
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2025-08-292025-08-298440241110.11646/palaeoentomology.8.4.8<strong>New fossil genera of Ricaniidae (Hemiptera: Fulgoromorpha) from the Roof of the World</strong>
https://www.mapress.com/pe/article/view/palaeoentomology.8.4.9
<p lang="en-US" align="justify"><span style="color: #000000;"><span style="font-family: Times New Roman, serif;"><span style="font-size: small;"><span style="color: #040305;">Two new monospecific genera of ricaniid planthoppers (Hemiptera: Fulgoromorpha: Ricaniidae) are described from the Paleocene deposits of the Niubao Formation, in the Dazhuoma area, Gangni Township, Qiangtang Basin of the Qinghai-Tibetan Plateau. The new genera are described</span><span style="color: #040305;">—</span><span style="color: #040305;"><em>Gshogpa</em></span> <span style="color: #040305;"><strong>gen. nov.</strong></span><span style="color: #040305;">, with </span><span style="color: #040305;"><em>Gshogpa linqibini</em></span> <span style="color: #040305;"><strong>sp. nov.</strong></span><span style="color: #040305;">, and </span><span style="color: #040305;"><em>Rdo</em></span> <span style="color: #040305;"><strong>gen. nov.</strong></span><span style="color: #040305;">, with </span><span style="color: #040305;"><em>Rdo gangniensis</em></span> <span style="color: #040305;"><strong>sp. nov.</strong></span><span style="color: #040305;"> This marks the</span> <span style="color: #040305;">first occurrence of Ricaniidae in these strata, and the earliest </span><span style="color: #040305;">fossil record of Ricaniidae in Asia. The following points are</span><span style="color: #040305;"> briefly discussed: the morphology of the tegmen venation of new fossils, their biogeographical significance as the first </span><span style="color: #040305;">extinct representatives of the family from Asia, and the fossil </span><span style="color: #040305;">record of Ricaniidae in the context of molecular divergence dating proposals.</span></span></span></span></p>ADAM STROIŃSKIJACEK SZWEDO
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2025-08-292025-08-298441242710.11646/palaeoentomology.8.4.9<strong><em>Anaspis</em> Geoffroy, 1762 subgenus <em>Spanisa</em> Emery, 1876 (Coleoptera: Scraptiidae) as Paleogene relicts</strong>
https://www.mapress.com/pe/article/view/palaeoentomology.8.4.10
<p lang="en-US" align="justify"><span style="color: #000000;"><span style="font-family: Times New Roman, serif;"><span style="font-size: small;"><span style="color: #000005;"><em>Anaspis </em></span><span style="color: #000005;">(</span><span style="color: #000005;"><em>Spanisa</em></span><span style="color: #000005;">) </span><span style="color: #000005;"><em>solodovnikovi </em></span><span style="color: #000005;"><strong>sp. nov.</strong></span><span style="color: #000005;">, the second known representative of its genus and subgenus from the late Eocene Rovno amber of Ukraine, is described and illustrated. The taxonomic position is confirmed, and supplementary description and images are provided for the Eocene Baltic amber </span><span style="color: #000005;"><em>A</em></span><span style="color: #000005;">.</span> <span style="color: #000005;">(</span><span style="color: #000005;"><em>Silaria</em></span><span style="color: #000005;">) </span><span style="color: #000005;"><em>parva </em></span><span style="color: #000005;">Abdullah, 1964. A key to extant and extinct species of the subgenus </span><span style="color: #000005;"><em>Spanisa </em></span><span style="color: #000005;">Emery, 1876 is presented for the first time. Morphology and new taxonomic </span><span style="color: #000005;">position of </span><span style="color: #000005;"><em>Anaspis</em></span><span style="color: #000005;"> (</span><span style="color: #000005;"><em>incertae sedis</em></span><span style="color: #000005;">) </span><span style="color: #000005;"><em>subhumerosa</em></span><span style="color: #000005;"> Franciscolo, 1954 are briefly discussed; this species is excluded from the </span><span style="color: #000005;">subgenus </span><span style="color: #000005;"><em>Spanisa</em></span><span style="color: #000005;">. Extant </span><span style="color: #000005;"><em>Spanisa</em></span><span style="color: #000005;"> species are allopatric, but in Rovno amber they are sympatric likely because of their adaptation to the ‘extinct’ equable Eocene climate. New faunistic records are provided for the extant </span><span style="color: #000005;"><em>A</em></span><span style="color: #000005;">.</span> <span style="color: #000005;">(</span><span style="color: #000005;"><em>Spanisa</em></span><span style="color: #000005;">) </span><span style="color: #000005;"><em>labiata </em></span><span style="color: #000005;">A. Costa, 1854</span> <span style="color: #000005;">and </span><span style="color: #000005;"><em>A</em></span><span style="color: #000005;">.</span> <span style="color: #000005;">(</span><span style="color: #000005;"><em>Spanisa</em></span><span style="color: #000005;">) </span><span style="color: #000005;"><em>subtilis</em></span><span style="color: #000005;"> Hampe, 1871. </span></span></span></span></p>DMITRY TELNOVEVGENY E. PERKOVSKY
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2025-08-292025-08-298442843810.11646/palaeoentomology.8.4.10<strong>Fast mandibles, sharp eyes: A new fossil species of <em>Odontomachus</em> (Latreille, 1804) gr. <em>cornutus</em> (Formicidae: Ponerinae) from Mexican amber formation</strong>
https://www.mapress.com/pe/article/view/palaeoentomology.8.4.11
<p lang="en-US" align="justify"><span style="color: #000000;"><span style="font-family: Times New Roman, serif;"><span style="font-size: small;"><em>Odontomachus</em> is a remarkable ant genus due to the fast mandibles with kinetic action, ocular prominences and pyriform head. Currently, there are three known fossil species, <em>O</em>.<em> paleomyagra</em> Wappler <em>et al</em>., a compression fossil from Czech Republic, <em>O</em>.<em> pseudobauri</em> De Andrade and <em>O</em>.<em> spinifer</em> De Andrade both from Dominican amber. Here, we describe the first Mexican fossil species from Chiapas amber formation and also the first gyne specimen, namely <em>Odontomachus angulops </em><strong>sp. nov.</strong> This species is the second described species for the <em>cornutus</em> group, also composed of the extant species <em>O</em>.<em> cornutus</em> Stitz. The ocular prominences forming angular projections, and the unique combination of wing venation characters and petiole shape, reinforce the <em>cornutus</em> group as a distinct taxon in the genus. We also discuss, based on the external morphology of the fossil, a phylogenetic hypothesis for the <em>cornutus</em> group placement in relation to the other Neotropical <em>Odontomachus</em> groups.</span></span></span></p>EDER CLEYTON BARBOSA FRANÇALUCAS ROBERTO PEREIRA GOMES
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2025-08-292025-08-298443944610.11646/palaeoentomology.8.4.11<strong>A new genus of diapriid wasp (Hymenoptera: Diaprioidea) from mid-Cretaceous Kachin amber with plesiomorphic fore wing venation</strong>
https://www.mapress.com/pe/article/view/palaeoentomology.8.4.12
<p lang="en-US" align="justify"><span style="color: #000000;"><span style="font-family: Times New Roman, serif;"><span style="font-size: small;"><span style="color: #040407;">The parasitoid wasp family Diapriidae, and the Belytinae subfamily in particular, are abundant in the fossil record, yet understudied. In this contribution, a new genus and species of belytine wasp is described and illustrated, based on two males from the Cenomanian Kachin amber: </span><span style="color: #040407;"><em>Eoaclista exquisita</em></span> <span style="color: #040407;"><strong>gen. et sp. nov.</strong></span><span style="color: #040407;"> The new taxon is particular as it retains the 1cu-a and 2cu-a veins as tubular on the fore wing, a character previously only found in the Monomachidae for the Diaprioidea superfamily. </span><span style="color: #040407;"><em>Eoaclista exquisita</em></span> <span style="color: #040407;"><strong>gen. et sp. nov.</strong></span><span style="color: #040407;"> shows that the 2cu-a vein was still present in early diverging Diapriidae, and that it has been lost at least three times in the family, and five times in the superfamily. It also highlights that the relationships within the Diaprioidea are still poorly understood and that wing characters should be treated with caution in a phylogenetic context. </span></span></span></span></p>MANUEL BRAZIDEC
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2025-08-292025-08-298444745810.11646/palaeoentomology.8.4.12<strong>A new genus of beaded lacewings (Neuroptera, Berothidae) from the mid-Cretaceous Kachin amber, with implications on the evolution of mouthparts and genital sclerites</strong>
https://www.mapress.com/pe/article/view/palaeoentomology.8.4.13
<p lang="en-US" align="justify"><span style="color: #000000;"><span style="font-family: Times New Roman, serif;"><span style="font-size: small;">A new genus, <em>Rhynchoberotha </em><strong>gen. nov.</strong> with two new species (<em>Rhynchoberotha zhangae</em><strong> sp. nov.</strong> and <em>Rhynchoberotha biyi</em><strong> sp. nov.</strong>) of the lacewing family Berothidae from the mid-Cretaceous Kachin amber are described. The new genus is closely related to <em>Aggregataberotha </em>Wang <em>et al</em>., 2023 and <em>Sejunctaberotha </em>Chen <em>et al</em>., 2024 by having similar forewing venation. Remarkably, the new genus is featured by the presence of a rostrum formed by the elongated chewing-mandibulate mouthparts. Another notable finding refers to the preservation of a mating pair of <em>R</em>. <em>biyi</em><strong> sp. nov.</strong>, which represents the first record of mating behaviour in fossil Neuroptera. Our new finding highlights the morphological diversity of Berothidae during the Cretaceous, and provides a new insight to the early evolution of mouthparts and genital sclerites.</span></span></span></p>YAN-QING WANGHONG-YU LIDE ZHUOCHUN-PENG XUXING-YUE LIU
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2025-08-292025-08-298445946910.11646/palaeoentomology.8.4.13<strong>An extraordinary ‘nogodinid’ planthopper (Hemiptera: Fulgoroidea) from the earliest Eocene Fur Fm. of Denmark</strong>
https://www.mapress.com/pe/article/view/palaeoentomology.8.4.1
<p lang="en-US" align="justify"><span style="color: #000000;"><span style="font-family: Times New Roman, serif;"><span style="font-size: small;"><span style="color: #040407;">The Ypresian Fur Formation in northwestern Denmark is one of the most famous and important sources of insect fossils from </span><span style="color: #040407;">the early Eocene (</span><span style="color: #040407;"><em>ca</em></span><span style="color: #040407;">.</span> <span style="color: #040407;">55–54 Ma, Pedersen </span><span style="color: #040407;"><em>et al</em></span><span style="color: #040407;">., 2012; Madsen & Rasmussen, 2021). The first insect fossils from the formation were described more than 100 years ago by Henriksen (1922), and today approximately 100 species have been described from more than 20,000 known fossils (TJS, JAR, RLS pers. observ.). Although the hemipteran suborder Auchenorrhyncha (cicadas, leafhoppers, planthoppers and allies) comprise one of the major components of this massive body of fossils (Rust, 1999; pers. unpublished obs.) only six species have been formally described to date. Of these the most recently described species, </span><span style="color: #040407;"><em>Archerythrogonia furensis</em></span><span style="color: #040407;"> Dietrich & Perkovsky, 2023 belongs to the infraorder Cicadomorpha (Dietrich & Perkovsky, 2023). The remaining five species all </span><span style="color: #040407;">belong to the infraorder Fulgoromorpha (Szwedo </span><span style="color: #040407;"><em>et al</em></span><span style="color: #040407;">., 2004).</span></span></span></span></p>THOMAS J. SIMONSENJAN A. RASMUSSENKENT OLSENRENÉ L. SYLVESTERSEN
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2025-08-292025-08-298435135410.11646/palaeoentomology.8.4.1<strong>Another species of <em>Palaeoglaesum</em> (Diptera, Psychodidae, Bruchomyiinae) from mid-Cretaceous Kachin amber</strong>
https://www.mapress.com/pe/article/view/palaeoentomology.8.4.2
<p lang="en-US" align="justify"><span style="color: #000000;"><span style="font-family: Times New Roman, serif;"><span style="font-size: small;"><span style="color: #000002;">Bruchomyiinae is a small subfamily of moth flies (Psychodidae) </span><span style="color: #000002;">which includes fewer than 60 species restricted to tropical and subtropical regions (Curler & Jacobson, 2012; Wagner & Stuckenberg, 2016; Wagner, 2017; Skibińska & Santos, 2023). Despite their low species diversity, representatives of this subfamily are relatively common in the fossil record. To date, 28 fossil species across five genera have been identified. All known fossil representatives are preserved as inclusions in various fossil resins, ranging in age from Lower Cretaceous Lebanese amber (Azar </span><span style="color: #000002;"><em>et al</em></span><span style="color: #000002;">., 2022) to Lower Miocene Dominican amber (Wagner, 2017). The genus </span><span style="color: #000002;"><em>Palaeoglaesum</em></span><span style="color: #000002;"> Wagner, 2017 is an extinct taxon known exclusively from Kachin amber, Myanmar. This genus comprises 15 species distributed in two subgenera: </span><span style="color: #000002;"><em>Palaeoglaesum </em></span><span style="color: #000002;">(</span><span style="color: #000002;"><em>Palaeoglaesum</em></span><span style="color: #000002;">) and </span><span style="color: #000002;"><em>Palaeoglaesum</em></span><span style="color: #000002;"> (</span><span style="color: #000002;"><em>Amplissimum</em></span><span style="color: #000002;">) (Skibińska & Santos, 2023). This genus is the most diverse fossil representative of this subfamily. Diagnostic characters of</span><span style="color: #000002;"><em> Palaeoglaesum</em></span><span style="color: #000002;"> include a small body size (approximately 2‒2.5 mm), dense setation, a head with a median longitudinal strip of setae, elongate mouthparts with prominent labellum, and an oval wing with a broadly rounded apex. The vein R</span><span style="color: #000002;"><sub>2+3</sub></span><span style="color: #000002;"> is at least twice as long as R</span><span style="color: #000002;"><sub>2</sub></span><span style="color: #000002;">, and the radial fork is positioned distally to the medial fork. Male genitalia exhibit either an elongated, apically bifurcated aedeagus or a short, non-bifurcated form, both surrounded at the base by a sleeve-like parameral sheath (Skibińska </span><span style="color: #000002;"><em>et al</em></span><span style="color: #000002;">., 2021; Skibińska & Santos, 2023). The high number of </span><span style="color: #000002;"><em>Palaeoglaesum</em></span><span style="color: #000002;"> species found in Kachin amber suggests that the tropical, near-coastal climate of the mid-Cretaceous Myanmar amber forest provided favorable conditions for a high diversity of Bruchomyiinae. Their ecology is closely associated with forest habitat, particularly tree hollows, forest litter, and tree trunks, </span><span style="color: #000002;">which likely contributed to their frequent preservation in amber. </span><span style="color: #000002;">The ongoing discoveries of new fossil taxa suggests that the diversity of Bruchomyiinae during the Cretaceous was likely much greater than it is today (Skibińska </span><span style="color: #000002;"><em>et al</em></span><span style="color: #000002;">., 2019, 2023).</span></span></span></span></p>SZYMON KACZMAREKWIESŁAW KRZEMIŃSKIAGNIESZKA SOSZYŃSKA
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2025-08-292025-08-298435535810.11646/palaeoentomology.8.4.2<strong><em>Meunieromyia</em>, a new genus of Medeterinae (Diptera: Dolichopodidae) from Eocene Baltic amber</strong>
https://www.mapress.com/pe/article/view/palaeoentomology.8.4.3
<p lang="en-US" align="justify"><span style="color: #000000;"><span style="font-family: Times New Roman, serif;"><span style="font-size: small;"><span style="color: #000003;">Until recently, the Eocene Baltic amber fauna of long-legged flies (Dolichopodidae) was superficially studied (Grichanov, 2023, 2024; Bickel & Martin, 2025). Most species described in 20 extant genera (Meunier, 1908) were placed by Grichanov in the following extinct genera of four extant subfamilies: </span><span style="color: #000003;">dolichopodine </span><span style="color: #000003;"><em>Prohercostomus </em></span><span style="color: #000003;">Grichanov, 1997, peloropeodine </span><span style="color: #000003;"><em>Palaeomedeterus </em></span><span style="color: #000003;">Meunier, 1895, sciapodine </span><span style="color: #000003;"><em>Wheelerenomyia </em></span><span style="color: #000003;">Meunier, 1907, and medeterine genera with the highest species richness, </span><span style="color: #000003;"><em>i</em></span><span style="color: #000003;">.</span><span style="color: #000003;"><em>e</em></span><span style="color: #000003;">., </span><span style="color: #000003;"><em>Medeterites </em></span><span style="color: #000003;">Grichanov, 2010, </span><span style="color: #000003;"><em>Palaeosystenus </em></span><span style="color: #000003;">Grichanov </span><span style="color: #000003;"><em>et al</em></span><span style="color: #000003;">., 2014, </span><span style="color: #000003;"><em>Plesiomedetera </em></span><span style="color: #000003;">Grichanov, 2023, and </span><span style="color: #000003;"><em>Systenites </em></span><span style="color: #000003;">Grichanov </span><span style="color: #000003;"><em>et al</em></span><span style="color: #000003;">., 2014. Recently, Bickel & Martin </span><span style="color: #000003;">(2025) described two more extinct medeterine genera, </span><span style="color: #000003;"><em>Kashubia</em></span> <span style="color: #000003;">Bickel, 2025 and </span><span style="color: #000003;"><em>Eridanomyia</em></span><span style="color: #000003;"> Bickel, 2025 with five species, </span><span style="color: #000003;">and nine extinct species of extant </span><span style="color: #000003;"><em>Atlatlia</em></span><span style="color: #000003;"> Bickel, 1986, all in the subfamily Medeterinae.</span></span></span></span></p>IGOR YA. GRICHANOV
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2025-08-292025-08-298435936210.11646/palaeoentomology.8.4.3