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In the vast abyssal plains northwest of Iceland, white glass sponges of the genus Caulophacus Schulze, 1886 were inhabited by reddish Bythocaris G.O. Sars, 1870 shrimps and pinkish amphipods. After in situ observations at 3700 m depth, in -1°C waters by a remotely operated vehicle, members of this assemblage were collected and preserved for molecular studies. Based on integrative taxonomic analyses, the amphipods were identified as a new species of the genus Halirages Boeck, 1871 – Halirages spongiae sp. nov. Lörz, Nack & Tandberg –, as described in detail below. Part of our integrative approach was to establish reference DNA barcodes for known species of Halirages. However, our investigation of material of Calliopiidae G.O. Sars, 1895 collected around Iceland and Norway revealed slight morphological discrepancies in all the described species of Halirages. Except for Halirages fulvocinctus (M. Sars, 1858), none of the encountered specimens of Calliopiidae fully matched a current species description. We illuminate the morphological characteristics of nine operational taxonomic units, which also represented clades in COI and 28S. We set the Icelandic samples in the context of Halirages from Canada and Norway. A key to the world species of Halirages is provided.
North-western Africa has a large Andrena fauna, but parts of the country away from coastal areas remain poorly studied, and confusion persists as to the identity of certain taxa due to the long history of study combined with imperfectly examined type material. New fieldwork, genetic barcoding, and study of museum material has substantially improved our understanding of this region. Eleven new species are described: A. (Aciandrena) bendai sp. nov., A. (Aciandrena) ifranensis sp. nov., A. (Euandrena) berberica sp. nov., A. (Hoplandrena) darha sp. nov., A. (Micrandrena) anammas sp. nov., A. (Micrandrena) gemina sp. nov., A. (Micrandrena) tinctoria sp. nov., and A. (incertae sedis) muelleri sp. nov., all from Morocco, and A. (Aciandrena) quieta sp. nov., A. (Euandrena) abscondita sp. nov., and A. (Taeniandrena) prazi sp. nov. from Morocco and Tunisia. Andrena (Aciandrena) nitidilabris Pérez, 1895 was misdiagnosed, and is actually the senior synonym of A. (Graecandrena) montarca parva Warncke, 1974 syn. nov. Andrena (Aciandrena) pisantyi sp. nov. is described from Algeria, Tunisia, and Israel, conforming to A. nitidilabris auctorum sensu Warncke. Andrena (Graecandrena) andina Warncke, 1974 stat. nov. and A. (Micrandrena) heliaca Warncke, 1974 stat. nov. are elevated from sub species to species status. Lectotypes are designated for A. (Melanapis) ephippium Spinola, 1838,
A. (Melanapis) rutila Spinola, 1838, A. (Simandrena) rhypara Pérez, 1903, and A. (Suandrena) savignyi Spinola, 1838. Neotypes are designated for A. (Melandrena) soror Dours, 1872 and A. (Notandrena) nigroviridula Dours, 1873. The female of A. (Aciandrena) triangulivalvis Wood, 2020 is described. The following seven additional synonymies are reported (senior name first): A. (Chrysandrena) testaceipes Saunders, 1908 = A. (Chrysandrena) rubricorpora Wood, 2021 syn. nov., A. (incertae sedis) maidaqi Scheuchl & Gusenleitner, 2007 = A. (Carandrena) hoggara Wood, 2021 syn. nov., A. (Lepidandrena) tuberculifera Pérez, 1895 = A. (Poecilandrena) nigriclypeus Wood, 2020 syn. nov., A. (Notandrena) albohirta Saunders, 1908 = A. (Notandrena) eddaensis Gusenleitner, 1998 syn. nov., A. (Notandrena) microthorax Pérez, 1895 = A. (Notandrena) nigrocyanea Saunders, 1908 syn. nov., A. (Simandrena) rhypara = A. (Simandrena) palumba Warncke, 1974 syn. nov., and A. (Taeniandrena) poupillieri Dours, 1872 = A. (Taeniandrena) lecerfi Benoist, 1961 syn. nov. Andrena (Notandrena) viridiaenea Pérez, 1903 is returned to synonymy with A. nigroviridula. Relative to the 2020 baseline, 16 Andrena species are newly recorded for Morocco, and six species are removed from the faunal list. These revisions bring the total number of Andrena species known from Morocco to 202 with 25 endemic species, making it one of the hotspots for Andrena diversity globally.
Within the well-studied Palearctic entomofauna, it is often assumed that the discovery of new species is limited to resolving cryptic species complexes within dark taxa. Herein, we describe a highly distinctive species of Aphanogmus Thomson, 1858 (Hymenoptera: Ceraphronidae) from Germany and provide a COI barcoding sequence for the new species. We present a 3D reconstruction of the holotype based on micro-CT to serve as a cybertype. The females of Aphanogmus kretschmanni Moser sp. nov. are diagnosed by two rows of prominent spines on the ventral edge of the 7th metasomal sternite, a character set that has not previously been found in Hymenoptera. We analyse the functional morphology of the ovipositor mechanism and discuss hypotheses regarding the functional implications of the unique modification of the 7th metasomal sternite. Possible host associations are reviewed and the taxonomic placement of the new species is discussed.
We describe a new troglophilic species of Filistata, F. betarif sp. nov. , collected from two caves in central Israel, by using light and electron microscopy and by DNA barcoding of the cytochrome c oxidase subunit I (COI) gene. Sequences of this gene show more than 15% of divergence between the new species and its sibling, F. insidiatrix (Forsskål, 1775), which is widely distributed across the Mediterranean and the Middle East. Notwithstanding, the two species are diagnosed only by a minor morphological detail in the embolic keel of the male pedipalp; females of both species are not diagnosable based only on morphology. We also find that samples of F. insidiatrix from different localities have large genetic divergence values (larger than 15% in some cases), but their pedipalps are identical in males; this suggests that F. insidiatrix might hide an additional cryptic diversity. We take this opportunity to provide a dichotomous key for identifying the crevice-weavers (Filistatidae) of Israel and Palestine.
Despite several decades of active research, there are still substantial gaps in the knowledge of parasitoid wasps in Australia, with many families and genera yet to be revised using modern approaches and only a fraction of the estimated fauna currently described. The genus Glyptapanteles Ashmead, 1904 is a member of the subfamily Microgastrinae (Hymenoptera: Braconidae) and all species in the subfamily are lepidopteran parasitoids. The genus previously contained only three species known from Australia: G. deliasa Austin & Dangerfield, 1992, G. drioplanetus Fagan-Jeffries & Austin, 2021 and G. mnesampela Austin, 2000. To undertake a revision of this morphologically-conserved group in Australia, we used a combination of molecular (cytochrome oxidase subunit one (COI) and wingless genes) and minimal morphological data to delimit and describe an additional 31 species: G. austini Fagan-Jeffries & Bird sp. nov. and the following 30 species all authored by Fagan-Jeffries, Bird & Austin: G. albigena sp. nov., G. andamookaensis sp. nov., G. arcanus sp. nov., G. aspersus sp. nov., G. austrinus sp. nov., G. baylessi sp. nov., G. bradfordae sp. nov., G. cooperi sp. nov., G. doreyi sp. nov., G. dowtoni sp. nov., G. eburneus sp. nov., G. erucadesolator sp. nov., G. ferrugineus sp. nov., G. foraminous sp. nov., G. goodwinnoakes sp. nov., G. guzikae sp. nov., G. harveyi sp. nov., G. kingae sp. nov., G. kittelae sp. nov., G. kurandaensis sp. nov., G. lambkinae sp. nov., G. lessardi sp. nov., G. mouldsi sp. nov., G. niveus sp. nov., G. rixi sp. nov., G. rodriguezae sp. nov., G. ruhri sp. nov., G. sanniopolus sp. nov., G. vergrandiacus sp. nov. and G. wrightae sp. nov. We provide a key to species groups and to the species able to be identified on morphological characters alone. Additionally, we provide a brief discussion of the difficulties in describing small, morphologically conserved wasps and the challenges associated with revising the taxonomy of hyperdiverse taxa in the context of the planned mission of Taxonomy Australia to accelerate the documentation of Australia’s biodiversity.
Arcola malloi (Pastrana, 1961) is a junior subjective synonym of Macrorrhinia endonephele (Hampson, 1918) syn. nov. (Lepidoptera: Pyralidae). The species is a biological control agent introduced in United States and Australia to control alligatorweed, Alternanthera philoxeroides (Mart.) Griseb. (Amaranthaceae). The synonymy is recognized by comparison of type specimens, genitalic dissections, and DNA COI barcoding. Vogtia Pastrana, 1961 syn. nov. and Arcola Shaffer, 1995 syn. nov. are synonymized with Macrorrhinia Ragonot, 1887. Macror-rhinia megajuxta (Neunzig and Goodson, 1992) comb. nov. is transferred from Ocala Hulst, 1892. Lectotypes are designated for Divitiaca ochrella Barnes and McDunnough, 1913, and Divitiaca simulella Barnes and Mc-Dunnough, 1913.
A new genus, Janzena (Erebidae), and 37 new species of Noctuoidea (Lepidoptera) are described from Florida as well as two species elevated from synonymy to species status. Bleptina biformata, Bleptina extincta, Bleptina flavivena, Bleptina verticalis, Lascoria coma, Janzena pyraliformis, Sigela sordes, Sigela minuta,Sigela incisa, Sigela subincisa, Sigela rosea, Sigela lynx, Dyspyralis ocala, Metalectra nigrior, Metalectra dixoni, Melipotis florida, Doryodes acta, Doryodes unica, Doryodes fulva, Toxonprucha killamae, Zale lafontainei,Zale vargoi, Zale clandestina, Athyrma fakahatchee, Antiblemma perva, Antiblemma carolae, Paectes hercules,Meganola georgei, Litoprosopus linea, Tripudia calusa, Catabenoides insularis, Neogalea caracara, Condica collaris, Homophoberia australis, Diastema leo, Pyreferra slotteni, and Leucania elephas are described as new. Hemeroplanis floccalis (Zeller), revived status, is raised to species status from the synonymy of Hemeroplanis scopulepes (Haworth),and Euscirrhopterus argentata (Druce), revived status, is raised to species status from the synonymy of Euscirrhopterus poeyi Grote. The genus Araeopteron Hampson is restricted to the Old World and Araeopteron vilhelmina (Dyar) is transferred to the genus Sigela Hulst, new combination. The barcode index number (BIN) is provided for each species, when available.
We recognize and review 40 species of Chlamydastis Meyrick, 1916 (Lepidoptera: Depressariidae) from Costa Rica, including four previously described (i.e., C. vividella (Busck, 1914), revived status; C. phytoptera (Busck, 1914); C. orion Busck, 1920; and C. ungulifera (Meyrick, 1929)) and 36 new species: C. abelulatei Phillips and Brown, new species; C. carolinagodoyae Phillips and Brown, new species; C. angelsolisi Phillips and Brown, new species; C. lindapitkinae Phillips and Brown, new species; C. iangauldi Phillips and Brown, new species; C. anniapicadoae Phillips and Brown, new species; C. antonioazofeifai Phillips and Brown, new species; C. mignondavisae Phillips and Brown, new species; C. marianofigueresi Phillips and Brown, new species; C. colleenhitchcockae Phillips and Brown, new species; C. bernardoespinozai Phillips and Brown, new species; C. bobandersoni Phillips and Brown, new species; C. carlosviquezi Phillips and Brown, new species; C. christerhanssoni Phillips and Brown, new species; C. christhompsoni Phillips and Brown, new species; C. paulhansoni Phillips and Brown, new species; C. elenaulateae Phillips and Brown, new species; C. gladysrojasae Phillips and Brown, new species; C. powelli Phillips and Brown, new species; C. gracewoodae Phillips and Brown, new species; C. juanmatai Phillips and Brown, new species; C. isidrochaconi Phillips and Brown, new species; C. jimlewisi Phillips and Brown, new species; C. jimmilleri Phillips and Brown, new species; C. montywoodi Phillips and Brown, new species; C. johnnoyesi Phillips and Brown, new species; C. luisdiegogomezi Phillips and Brown, new species; C. paulthiaucourti Phillips and Brown, new species; C. dondavisi Phillips and Brown, new species; C. irenecanasae Phillips and Brown, new species; C. manuelzumbadoi Phillips and Brown, new species; C. noramartinae Phillips and Brown, new species; C. vitorbeckeri Phillips and Brown, new species; C. ronaldzunigai Phillips and Brown, new species; C. munifigueresae Phillips and Brown, new species; and C. willsflowersi Phillips and Brown, new species.COI nucleotide sequences (“DNA barcodes”) were obtained for 33 of the species, which helped associate males with females for sexually dimorphic species and revealed a few cryptic, presumably evolutionary siblings. We illustrate adults of all species, along with their male and female genitalia, where available.Nineteen species were reared from caterpillars, and their foodplants are listed. In Costa Rica, 15 species of Chlamydastis are recorded exclusively from Sapotaceae; one species each exclusively from Clethraceae, Vochysiaceae, Combretaceae, and Melastomataceae. Larvae are illustrated for 10 of the 36 new species, and superficial larval descriptions are provided based on photographs and notes. Of the 40 species of Chlamydastis reported from Costa Rica, 32 have been light-collected or reared from Área de Conservación Guanacaste.
Platystasius transversus (Thomson) (Hymenoptera: Platygastridae) is a rarely collected egg parasitoid of Leptura aurulenta Fabricius (Coleoptera: Cerambycidae). Four female specimens were found in Germany, a new country record for the genus and species. Illustrations, DNA barcodes, and an updated distribution are provided. We review its taxonomic history, biology, and ecological associations.