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 press en-US Palaeoentomology 2624-2826 <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>An early Miocene prominent moth from Bílina mine in the Czech Republic (Lepidoptera: Notodontidae)</strong> https://www.mapress.com/pe/article/view/palaeoentomology.8.5.2 <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: #05050a;">Prominent moths (Lepidoptera: Notodontidae) are </span><span style="color: #05050a;">morphologically and ecologically diverse members of the </span><span style="color: #05050a;">superfamily Noctuoidea, the largest radiation of extant </span><span style="color: #05050a;">Lepidoptera on Earth with more than 40,000 described species</span><span style="color: #05050a;"> (van Nieukerken </span><span style="color: #05050a;"><em>et al</em></span><span style="color: #05050a;">., 2011). The phylogenetic relations are </span><span style="color: #05050a;">yet unclear between Notodontidae and the other six recognized </span><span style="color: #05050a;">noctuoid families (Scranciidae, Oenosandridae, Noctuidae, Erebidae, Euteliidae, and Nolidae) (Zahiri </span><span style="color: #05050a;"><em>et al</em></span><span style="color: #05050a;">., 2011; St </span><span style="color: #05050a;">Laurent </span><span style="color: #05050a;"><em>et al</em></span><span style="color: #05050a;">., 2024). Recent higher-level molecular phylogenies</span> <span style="color: #05050a;">recovered Notodontidae sister to a clade formed by Noctuidae, Erebidae, Euteliidae, and Nolidae (Zahiri </span><span style="color: #05050a;"><em>et al</em></span><span style="color: #05050a;">., 2011; Wahlberg </span><span style="color: #05050a;"><em>et al</em></span><span style="color: #05050a;">., 2013; Kawahara </span><span style="color: #05050a;"><em>et al</em></span><span style="color: #05050a;">., 2019; Rota </span><span style="color: #05050a;"><em>et al</em></span><span style="color: #05050a;">., 2022; St Laurent </span><span style="color: #05050a;"><em>et al</em></span><span style="color: #05050a;">., 2024). However, due to poor taxon sampling and the scarcity of noctuoid fossils, the molecular-clock estimates for </span><span style="color: #05050a;">the divergence between Notodontidae and other extant noctuoid </span><span style="color: #05050a;">families remain highly uncertain, probably in the range of 67–88 Mya (Wahlberg </span><span style="color: #05050a;"><em>et al</em></span><span style="color: #05050a;">., 2013; Kawahara </span><span style="color: #05050a;"><em>et al</em></span><span style="color: #05050a;">., 2019).</span></span></span></span></p> JAKUB PROKOP PÁVEL MATOS-MARAVÍ Copyright (c) 2025 Magnolia press limited 2025-10-31 2025-10-31 8 5 476 479 10.11646/palaeoentomology.8.5.2 <strong>Redescription of the only known Korean specimen of <em>Turbidapsyche dobrokhotovae</em> (Novokshonov, 1997) from the Amisan Formation</strong> https://www.mapress.com/pe/article/view/palaeoentomology.8.5.3 <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: #040409;">The mecopteran family Mesopsychidae is characterized primarily by an elongated siphonate proboscis, which likely enabled its members to feed on and pollinate Mesozoic gymnosperms (</span><span style="color: #040409;"><em>e</em></span><span style="color: #040409;">.</span><span style="color: #040409;"><em>g</em></span><span style="color: #040409;">., Labandeira </span><span style="color: #040409;"><em>et al</em></span><span style="color: #040409;">., 2007; Ren </span><span style="color: #040409;"><em>et al</em></span><span style="color: #040409;">., 2009). However, many species and fossil specimens from this family are known only from isolated wings, making it difficult to generalize their paleoecology (Lian </span><span style="color: #040409;"><em>et al</em></span><span style="color: #040409;">., 2024). </span></span></span></span></p> CORENTIN JOUAULT XIN-NENG LIAN GI-SOO NAM Copyright (c) 2025 Magnolia press limited 2025-10-31 2025-10-31 8 5 480 482 10.11646/palaeoentomology.8.5.3 <strong>First clown beetle (Coleoptera: Histeridae) from Middle Miocene Mexican amber</strong> https://www.mapress.com/pe/article/view/palaeoentomology.8.5.4 <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: #030304;">The polyphagan family of clown beetles (Coleoptera: Histeridae) is represented by over 4,800 species with worldwide distribution. It is well-known for the diversity of exploited habitats and remarkable morphological adaptations, which </span><span style="color: #030304;">evolved in relation to habitat shifts (Kovarik &amp; Caterino, 2016). The origin of the family has been estimated to the mid-Jurassic</span> <span style="color: #030304;">based on phylogenomic analyses (Kusý </span><span style="color: #030304;"><em>et al</em></span><span style="color: #030304;">., 2025). The earliest known fossils appeared in the Cretaceous Period, with the oldest </span><span style="color: #030304;">fossils from the Lower Cretaceous Hkamti amber (</span><span style="color: #030304;"><em>ca</em></span><span style="color: #030304;">. 110 Ma) of northern Myanmar (Caterino &amp; Yamamoto, 2023; Simon-Pražák </span><span style="color: #030304;"><em>et al</em></span><span style="color: #030304;">., 2024). There are currently over 50 described fossil species of clown beetles with most of them found in Cretaceous and Eocene ambers. Only a single species has been formally described from the Miocene age ambers (</span><span style="color: #030304;"><em>i</em></span><span style="color: #030304;">.</span><span style="color: #030304;"><em>e</em></span><span style="color: #030304;">., </span><span style="color: #030304;"><em>Trypanaeus hispaniolus</em></span><span style="color: #030304;"> Chatzimanolis </span><span style="color: #030304;"><em>et al</em></span><span style="color: #030304;">., 2006; from Middle Miocene Dominican amber of the Dominican Republic).</span></span></span></span></p> JAN SIMON-PRAŽÁK SHÛHEI YAMAMOTO JAKUB PROKOP ALEXEY K. TISHECHKIN Copyright (c) 2025 Magnolia press limited 2025-10-31 2025-10-31 8 5 483 486 10.11646/palaeoentomology.8.5.4 <strong>Merging part and counterpart images of compression fossils</strong> https://www.mapress.com/pe/article/view/palaeoentomology.8.5.5 <p lang="en-US" align="justify"><span style="color: #000000;"><span style="font-family: Times New Roman, serif;"><span style="font-size: small;">While examining rich insect collections from the Lower Permian Chekarda locality in the Cis-Urals region of Russia, preserved at the Paleontological Institute (PIN) in Moscow, I noticed that dark patches, representing fragments of fossilized cuticle upon a lighter rock matrix, on the part and the counterpart of one fossil often appeared complementary and could be fitted together like a jigsaw puzzle. The phenomenon is well familiar to those who study thin compression fossils. Insects, for example, occasionally become compressed by sediment to such a state that the multiple cuticular layers of their bodies—opposite body sides, overlapping wings, legs, and other appendages—all become fused into a single film of fossilized cuticle. Then, a blow of the rock hammer fractures this film in such a way that some of its fragments become exposed upon the part and others upon the counterpart. I attempted to combine such part and counterpart images into more complete composites and in this way I was able to interpret many poorly preserved specimens, which otherwise would be left out of the study, and, moreover, to see and understand morphological structures of crucial importance, which otherwise would be overlooked. The results of my palaeoentomological study will be published elsewhere, but my success in superposition of part and counterpart images warrants a separate, brief publication on the method itself. Undoubtedly the idea must have occurred to many. Merged composites of part and counterpart images and descriptions of the implemented merging techniques have been published as part of larger studies (<em>e</em>.<em>g</em>., Haug <em>et al</em>., 2009; Haug &amp; Haug, 2013). Yet, I believe the method deserves a dedicated discussion. It has some limitations, which confine the scope of its use, but in some cases it may help visualize poorly preserved, badly fragmented specimens, which may otherwise remain uninterpretable. Therefore, the goal of the present note is to describe a simple method of part-counterpart (PCP) image merging and discuss its pitfalls and limitations. The images were processed manually using either of two computer graphics editors, the proprietary Adobe Photoshop and the free open-source GIMP. In this form, the technique is available to virtually anyone. On the other hand, its computer automation appears to be a realistic goal.</span></span></span></p> ROMAN RAKITOV Copyright (c) 2025 Magnolia press limited 2025-10-31 2025-10-31 8 5 487 490 10.11646/palaeoentomology.8.5.5 <strong>A new species of <em>Cretevania</em> (Hymenoptera: Evaniidae) preserved in Albian amber of El Soplao (Cantabria, Spain)</strong> https://www.mapress.com/pe/article/view/palaeoentomology.8.5.6 <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;">A new species of the diverse extinct genus </span><span style="color: #000003;"><em>Cretevania</em></span><span style="color: #000003;"> Rasnitsyn, 1975, </span><span style="color: #000003;"><em>Cretevania orgonomecorum</em></span><span style="color: #000003;"> Peñalver &amp; Sánchez-García </span><span style="color: #000003;"><strong>sp. nov.</strong></span><span style="color: #000003;">, is described from Spanish Lower Cretaceous (middle Albian) amber from El Soplao, based on a single, complete and well-preserved female. The new species is compared with other known species of the genus, mainly those with similar wing shape and venation, large body size, and those described from Albian Spanish amber. This new species is among the largest within the genus and similar in body length to </span><span style="color: #000003;"><em>C</em></span><span style="color: #000003;">.</span><span style="color: #000003;"><em> tenuis</em></span><span style="color: #000003;"> from Cenomanian Kachin amber (Myanmar) and </span><span style="color: #000003;"><em>C</em></span><span style="color: #000003;">.</span><span style="color: #000003;"><em> pristina</em></span><span style="color: #000003;"> from Barremian compression rocks of Beipiao (China). Its description and the revision of other species have led to the identification of previously unrecognized characters which may be useful in future taxonomic diagnoses. These results contribute to a more accurate understanding of interspecific differences and will help delimit species boundaries within a genus, proving increasingly diverse in the Cretaceous. The previously established synonymisation of the genus </span><span style="color: #000003;"><em>Procretevania</em></span><span style="color: #000003;"> as junior to </span><span style="color: #000003;"><em>Cretevania</em></span><span style="color: #000003;"> is also reviewed here. Palaeobiological comments are provided based on anatomical features of the genus.</span></span></span></span></p> ENRIQUE PEÑALVER XAVIER DELCLÒS SERGIO ÁLVAREZ-PARRA RICARDO PÉREZ-DE LA FUENTE ALBA SÁNCHEZ-GARCÍA Copyright (c) 2025 Magnolia press limited 2025-10-31 2025-10-31 8 5 491 501 10.11646/palaeoentomology.8.5.6 <strong>New damselflies (†Mesostictinae and Platycnemidinae) from Cretaceous Burmese amber</strong> https://www.mapress.com/pe/article/view/palaeoentomology.8.5.7 <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: #040407;">Damselflies (suborder Zygoptera) are very diverse in extant ecosystems and contain more than 20 fossil species into eleven families in Burmese amber. Here we describe two fossil damselflies from the Cenomanian Burmese amber that we attributed to the families Platystictidae and </span><span style="color: #040407;">Platycnemididae. The research focused on specimens housed</span> <span style="color: #040407;">at the Geominer Museum of the Instituto Geológico y Minero</span><span style="color: #040407;"> de España, Consejo Superior de Investigaciones Científicas (IGME, CSIC) in Madrid. The results of the study identified two new taxa, </span><span style="color: #040407;"><em>Mesosticta garciavallsi </em></span><span style="color: #040407;"><strong>sp. </strong></span><span style="color: #040407;"><strong>nov. </strong></span><span style="color: #040407;">and an undetermined Platycnemididae species, or new</span><span style="color: #040407;"> morphotype, which have been studied based on their fore- and hind wing venations, being the wings the only parts preserved. These new specimens represent the fifth species described of the extinct genus </span><span style="color: #040407;"><em>Mesosticta</em></span><span style="color: #040407;"> Huang, Azar, Cai &amp; Nel, 2015 and the putative oldest fossil record of Platycnemidinae. Our findings increase the known diversity of damselflies during the mid-Cretaceous.</span></span></span></span></p> MATEO D. MONFERRAN ENRIQUE PEÑALVER ANDRÉ NEL Copyright (c) 2025 Magnolia press limited 2025-10-31 2025-10-31 8 5 502 511 10.11646/palaeoentomology.8.5.7 <strong>Two new Jurassic species of Tipuloidea (Insecta: Diptera) from Daohugou Village, China</strong> https://www.mapress.com/pe/article/view/palaeoentomology.8.5.8 <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: #040408;">Two new species of Tipuloidea, </span><span style="color: #040408;"><em>Tipunia ningchengensis</em></span> <span style="color: #040408;"><strong>sp. nov.</strong></span><span style="color: #040408;"> and </span><span style="color: #040408;"><em>Praearchitipula procera</em></span> <span style="color: #040408;"><strong>sp. nov.</strong></span><span style="color: #040408;"> are described and illustrated from the Middle Jurassic Jiulongshan Formation</span><span style="color: #040408;"> at Daohugou Village, Inner Mongolia, China. The new species </span><span style="color: #040408;"><em>T</em></span><span style="color: #040408;">. </span><span style="color: #040408;"><em>ningchengensis</em></span> <span style="color: #040408;"><strong>sp. nov.</strong></span><span style="color: #040408;"> is not only the first Chinese record of genus </span><span style="color: #040408;"><em>Tipunia</em></span><span style="color: #040408;">, but also the first record of Tipulidae in the Middle Jurassic. Thereby, it not only enriches the diversity and distribution area of </span><span style="color: #040408;"><em>Tipunia</em></span><span style="color: #040408;">, but also extends the first appearance of Tipulidae back to the Middle Jurassic. The new pediciid species </span><span style="color: #040408;"><em>P</em></span><span style="color: #040408;">.</span><span style="color: #040408;"><em> procera</em></span> <span style="color: #040408;"><strong>sp. nov.</strong></span><span style="color: #040408;"> found without hairy eyes, confirms once again that the Mesozoic genus </span><span style="color: #040408;"><em>Praearchitipula</em></span><span style="color: #040408;"> has no pubescence of the eyes, different than the extant genera of Pediciidae. These two new species further enhance the biodiversity of Jurassic insects in the Daohugou area, and the suitable and diverse ecological environment of this region harbored so rich and diverse insect groups.</span></span></span></span></p> CHU-PING WANG YU-SHUANG LIU Copyright (c) 2025 Magnolia press limited 2025-10-31 2025-10-31 8 5 512 519 10.11646/palaeoentomology.8.5.8 <strong>Thripidae and Melanthripidae from the mid-Cretaceous (Insecta: Thysanoptera)</strong> https://www.mapress.com/pe/article/view/palaeoentomology.8.5.9 <p lang="en-US" align="justify"><span style="color: #000000;"><span style="font-family: Times New Roman, serif;"><span style="font-size: small;">The thrips diversity preserved in Kachin amber is remarkably high, with numerous new species awaiting discovery. In this paper, two new species of Thripidae: <em>Euthythrips longialatus</em> <strong>gen. et sp. nov.</strong> and <em>Minythrips </em><em>exquisitus</em><strong> gen. et sp. nov.</strong>, plus five new species of Melanthripidae: <em>Aspistothrips fortis</em> <strong>gen. et sp. nov.</strong>, <em>Aspistothrips decorus</em> <strong>sp. nov.</strong>, <em>Areiothrips bellator</em> <strong>gen. et sp. nov.</strong>, <em>Charismathrips longiantennatus</em> <strong>gen. et sp. </strong><strong>nov.</strong>, <em>Charismathrips exaridus</em> <strong>sp. nov.</strong>, are systematically described, expanding the fossil record of Thysanoptera from Kachin amber. Through comparative morphological analyses of fossil taxa, we propose that two characters likely represent plesiomorphic traits of Thysanoptera: nine antennomeres and duplicated cilia arranged parallel to regular fringe cilia. By synthesizing existing research on thrips environmental interactions, this study briefly analyzes the adaptive evolution of thrips during floral ecosystem turnover.</span></span></span></p> DA-WEI GUO MICHAEL S. ENGEL CHUNGKUN SHIH YU-RONG JIANG DONG REN Copyright (c) 2025 Magnolia press limited 2025-10-31 2025-10-31 8 5 520 537 10.11646/palaeoentomology.8.5.9 <strong><em>Cretofigulus</em> (Coleoptera: Lucanidae: Lucaninae): a new genus with two new species in mid-Cretaceous amber from northern Myanmar</strong> https://www.mapress.com/pe/article/view/palaeoentomology.8.5.10 <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 fossil stag beetle genus, <em>Cretofigulus </em><strong>gen. nov.</strong>, is identified and described from mid-Cretaceous Kachin amber from northern Myanmar. Two new species, <em>C</em>.<em> caoqiangi </em><strong>sp. nov.</strong> and <em>C</em>. <em>hollowayae </em><strong>sp. nov.</strong> are herein described and illustrated. Additionally, the morphological differences between <em>Cretofigulus </em><strong>gen. </strong><strong>nov.</strong> and the related extant genus <em>Figulus </em>Macleay, 1819 are discussed. <em>Cretofigulus </em><strong>gen. nov.</strong> is the second fossil record of the subfamily Lucaninae from Burmese amber. Despite an evolutionary divergence of approximately 99 million years, <em>Cretofigulus</em> <strong>gen. nov.</strong> exhibits a striking morphological resemblance to extant <em>Figulus</em>. Key diagnostic features of <em>Cretofigulus</em> <strong>gen. nov.</strong>, including reduced sexual dimorphism, suggest behavioral and ecological parallels with modern Figulini Burmeister, 1847, such as carnivorous feeding habits and adaptation to a monogamous lifestyle within decaying wood.</span></span></span></p> ZHI-HAO QI CINZIA MONTE CHEN-YANG CAI HAI-TIAN SONG GUANG-HONG LIANG Copyright (c) 2025 Magnolia press limited 2025-10-31 2025-10-31 8 5 538 551 10.11646/palaeoentomology.8.5.10 <strong>A new extinct species of <em>Phloiotrya</em> Stephens (Coleoptera: Melandryidae: Dircaeini) from late Eocene Rovno amber</strong> https://www.mapress.com/pe/article/view/palaeoentomology.8.5.11 <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;">A new fossil species of the melandryine beetle genus </span><span style="color: #000005;"><em>Phloiotrya</em></span><span style="color: #000005;"> from Rovno amber is described and illustrated. The new species, </span><span style="color: #000005;"><em>Phloiotrya</em></span><span style="color: #000005;"> (</span><span style="color: #000005;"><em>Phloiotrya</em></span><span style="color: #000005;">) </span><span style="color: #000005;"><em>groehni </em></span><span style="color: #000005;"><strong>sp. nov.</strong></span><span style="color: #000005;">, is compared with its extant congeners and related extinct taxa from Baltic amber. Additional fossil records of false darkling beetles from Eocene Rovno and Baltic fossil resins are presented.</span></span></span></span></p> VITALII ALEKSEEV ANDRIS BUKEJS Copyright (c) 2025 Magnolia press limited 2025-10-31 2025-10-31 8 5 552 559 10.11646/palaeoentomology.8.5.11 <strong>A revision of the fossil true bugs <em>Mesolygaeus</em> Ping, 1928 and <em>Mongolocoris</em> Ryzhkova, 2012 (Hemiptera: Heteroptera: Enicocoridae) with description of a new species</strong> https://www.mapress.com/pe/article/view/palaeoentomology.8.5.12 <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: #030304;">The Early Cretaceous genus </span><span style="color: #030304;"><em>Mesolygaeus</em></span><span style="color: #030304;"> Ping, 1928 is revised based on numerous specimens from the Lower Cretaceous Laiyang Formation in the Laiyang Basin, eastern Shandong Province, China. The genus </span><span style="color: #030304;"><em>Enicocoris </em></span><span style="color: #030304;">Popov, 1980 is recognized as a junior synonym of </span><span style="color: #030304;"><em>Mesolygaeus </em></span><span style="color: #030304;"><strong>syn. nov</strong></span><span style="color: #030304;">. and the family Mesolygaeidae, 1990 is therefore recognized as a junior synonym of Enicocoridae Popov, 1980 </span><span style="color: #030304;"><strong>syn. nov. </strong></span><span style="color: #030304;">Also, the genus </span><span style="color: #030304;"><em>Longyanteclypea</em></span><span style="color: #030304;"> Zhang </span><span style="color: #030304;"><em>et </em></span><span style="color: #030304;"><em>al</em></span><span style="color: #030304;">., 2013 is considered as a junior synonym of </span><span style="color: #030304;"><em>Mongolocoris</em></span> <span style="color: #030304;">Ryzhkova, 2012 </span><span style="color: #030304;"><strong>syn. nov. </strong></span><span style="color: #030304;">Additionally, a new species, </span><span style="color: #030304;"><em>Mongolocoris polhemi</em></span><span style="color: #030304;"> Ryzhkova </span><span style="color: #030304;"><strong>sp. nov.</strong></span><span style="color: #030304;">, is described from</span><span style="color: #030304;"> the Lower Cretaceous Tsagaantsab Formation of Tsagaan-Suburga, Dornogovi Province, southeastern Mongolia.</span></span></span></span></p> OLGA V. RYZHKOVA ELENA S. IVANOVA HAI-CHUN ZHANG Copyright (c) 2025 Magnolia press limited 2025-10-31 2025-10-31 8 5 560 569 10.11646/palaeoentomology.8.5.12 <strong>The oldest fossil record of jump tree bug from mid-Cretaceous amber (Insecta: Hemiptera: Miridae)</strong> https://www.mapress.com/pe/article/view/palaeoentomology.8.5.13 <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: #040408;">A new tribe Cretaloxini </span><span style="color: #040408;"><strong>tribe. nov.</strong></span><span style="color: #040408;"> of jumping tree bugs is established for the fossil</span><span style="color: #040408;"><em> Cretaloxus wanae</em></span> <span style="color: #040408;"><strong>gen. et sp. nov.</strong></span><span style="color: #040408;">, </span><span style="color: #040408;">a well-preserved specimen from mid-Cretaceous amber. This taxon is classified within the subfamily Isometopinae (Hemiptera: Miridae) and represents the oldest fossil record </span><span style="color: #040408;">of Isometopinae found so far from northern Myanmar as well </span><span style="color: #040408;">as the whole world. High-resolution habitus photographs of the female holotype (</span><span style="color: #040408;"><em>Cretaloxus wanae</em></span> <span style="color: #040408;"><strong>gen. et sp. nov.</strong></span><span style="color: #040408;">) are provided. The new species can be placed in </span><span style="color: #040408;">Isometopinae by the following characters: the ocelli present and antennal fossa situated below compound eyes. The fossil </span><span style="color: #040408;">serves as a critical source of morphological data, offering novel insights for analyzing the phylogenetic relationships within Miridae through external characters. Specifically, this mid-Cretaceous Burmese fossil may preserve an early morphological stage of Isometopinae, offering key evidence for reconstructing the initial diversification of Miridae.</span></span></span></span></p> JIA-DONG YIN WEN-JUN BU QIANG XIE Copyright (c) 2025 Magnolia press limited 2025-10-31 2025-10-31 8 5 570 577 10.11646/palaeoentomology.8.5.13 <strong>A new species of <em>Chrysopilus</em> Macquart, 1826 (Diptera, Rhagionidae) from Baltic amber</strong> https://www.mapress.com/pe/article/view/palaeoentomology.8.5.14 <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: #040408;">A new species of rhagionid fly, </span><span style="color: #040408;"><em>Chrysopilus perseverans</em></span> <span style="color: #040408;"><strong>sp. nov.</strong></span><span style="color: #040408;">, is described from middle Eocene Baltic amber. Based </span><span style="color: #040408;">on the key provided by Kerr (2010), the new species can be attributed to the genus </span><span style="color: #040408;"><em>Chrysopilus</em></span><span style="color: #040408;"> Macquart, 1826 due to the following diagnostic characters: antennae with a long terminal arista, dense microsetae on arista, holoptic male eyes, setose anepisternum and laterotergite, and macrosetae on forefemur. A checklist of named species of fossil rhagionids is provided.</span></span></span></span></p> CHEN-XIN ZHOU QI FENG QIANG YANG YONG-JIE WANG DONG REN CHAO-FAN SHI Copyright (c) 2025 Magnolia press limited 2025-10-31 2025-10-31 8 5 578 586 10.11646/palaeoentomology.8.5.14 <strong>A new species of dustywings from the Lower Cretaceous Hammana outcrop of Lebanon (Neuroptera: Coniopterygidae)</strong> https://www.mapress.com/pe/article/view/palaeoentomology.8.5.15 <p lang="en-US" align="justify"><span style="color: #000000;"><span style="font-family: Times New Roman, serif;"><span style="font-size: small;"><em>Libanoconis medialis</em> <strong>sp. nov.</strong> from the Mdeyrij-Hammana outcrop of amber (Central Lebanon), is characterised, illustrated, described and its taxonomic position is discussed. <em>Libanoconis medialis</em> <strong>sp. nov. </strong>is the third coniopterygid from the Lebanese amber. The new species, as well as the reexamination of the holotype of <em>L. fadiacra</em> from Bkassine, Jezzine District, permits to clarify the presence of a trifurcate MP in the hind wing.</span></span></span></p> DANY AZAR MICHAEL S. ENGEL Copyright (c) 2025 Magnolia press limited 2025-10-31 2025-10-31 8 5 587 593 10.11646/palaeoentomology.8.5.15 <strong>Two new thorny stick insects (Euphasmatodea) from mid-Cretaceous Kachin amber</strong> https://www.mapress.com/pe/article/view/palaeoentomology.8.5.16 <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: #05050a;">Two new species of thorny stick insects are described and figured, belonging to the genus </span><span style="color: #05050a;"><em>Echinosomiscus</em></span><span style="color: #05050a;"> Engel, 2016 (Euphasmatodea: Phasmatidae: Echinosomiscinae). </span><span style="color: #05050a;"><em>Echinosomiscus conicaculeatus</em></span> <span style="color: #05050a;"><strong>sp. nov.</strong></span><span style="color: #05050a;"> and </span><span style="color: #05050a;"><em>E</em></span><span style="color: #05050a;">.</span><span style="color: #05050a;"><em> longianalis</em></span> <span style="color: #05050a;"><strong>sp. nov.</strong></span><span style="color: #05050a;"> are both from mid-Cretaceous Kachin amber and preserve apomorphies of this genus, such as the similar </span><span style="color: #05050a;">coronal acanthae on the head, a scape with two dorsal thorns, thoracic spines arranged transversely, and tarsomere V longer</span><span style="color: #05050a;"> than the remaining tarsomeres. These two new species have</span><span style="color: #05050a;"> different and distinctive arrangements of acanthae on the head, thorax, and legs relative to </span><span style="color: #05050a;"><em>E</em></span><span style="color: #05050a;">.</span><span style="color: #05050a;"><em> primoticus</em></span><span style="color: #05050a;"> Engel &amp; </span><span style="color: #05050a;">Wang, 2016. Most notably, </span><span style="color: #05050a;"><em>E</em></span><span style="color: #05050a;">.</span><span style="color: #05050a;"><em> longianalis</em></span><span style="color: #05050a;"> lacks spines on </span><span style="color: #05050a;">the abdomen, and tergum X is undivided </span><span style="color: #05050a;"><em>vs</em></span><span style="color: #05050a;">. numerous spines </span><span style="color: #05050a;">on the abdomen, and tergum X divided into hemitergites in </span><span style="color: #05050a;"><em>E</em></span><span style="color: #05050a;">.</span> <span style="color: #05050a;"><em>primoticus</em></span><span style="color: #05050a;">. The discovery of these new specimens broadens the evidence of spines as a defensive mechanism in the mid-Cretaceous forest ecosystems.</span></span></span></span></p> MENG ZHANG MICHAEL S. ENGEL DONG REN HONG-RU YANG Copyright (c) 2025 Magnolia press limited 2025-10-31 2025-10-31 8 5 594 603 10.11646/palaeoentomology.8.5.16 <strong>Modelling among-site compositional heterogeneity resolves ant backbone phylogeny: A reply to Boudinot & Lieberman (2025)</strong> https://www.mapress.com/pe/article/view/palaeoentomology.8.5.1 <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: #000002;">Understanding the early evolution of ants has been hindered by conflicting phylogenetic hypotheses and methodological</span><span style="color: #000002;"> inconsistencies across studies. In Cai (2024), I reanalyzed both Sanger-sequencing and genome-scale datasets of ants using rigorous model comparison and methods that account for among-site compositional heterogeneity to identify the sources of phylogenetic conflict. The results showed that the 11-loci datasets in Borowiec </span><span style="color: #000002;"><em>et al</em></span><span style="color: #000002;">. (2019) failed to resolve deep ant relationships and could not determine the position of </span><span style="color: #000002;"><em>Martialis heureka</em></span><span style="color: #000002;">. Analyses of the genome-scale data further revealed that the placement of key lineages depends </span><span style="color: #000002;">strongly on model fit. Bayesian cross-validation and posterior predictive assessments demonstrated that the infinite mixture </span><span style="color: #000002;">CAT-GTR+G4 model substantially outperforms empiri</span><span style="color: #000002;">cal finite mixture models, providing robust support for the Leptanillinae-sister hypothesis. Criticisms by Boudinot &amp; Lieberman (2025) regarding the study design, model choice, and convergence assessments stem from misinterpretations of the analytical framework. The matrices in Cai (2024) were explicitly designed to test model performance under controlled subsampling and filtering schemes, and all analyses showed consistent results across datasets. The findings reaffirm that accurately modelling among-site compositional heterogeneity is essential for resolving the backbone phylogeny of ants, and that under the best-fitting </span><span style="color: #000002;">models, </span><span style="color: #000002;"><em>Martialis heureka</em></span><span style="color: #000002;"> occupies a well-supported </span><span style="color: #000002;">position as sister to all non-leptanilline ants.</span></span></span></span></p> CHEN-YANG CAI Copyright (c) 2025 Magnolia press limited 2025-10-31 2025-10-31 8 5 471 475 10.11646/palaeoentomology.8.5.1