Search

We record for the first time the families Stephanidae and Mymarommatidae and the corresponding superfamilies Stephanoidea and Mymarommatoidea in Georgia. A single female of Stephanus serrator (Fabricius, 1798) was collected in Kakheti, Lagodekhi Protected Area (LPA), in the east, and five individuals of Mymaromma anomalum (Blood & Kryger, 1922) were collected in Achara, Kintrishi National Park (KNP), in the west of Georgia. Each of the studied wasp species is complemented by DNA (CO1) barcode sequences. Vouchers are deposited at Museum Koenig Bonn (LIB, ZFMK) and the Entomology Collection of the Agricultural University of Georgia (ECAUG).

The genus Anacharis Dalman, 1823 comprises parasitoid wasps that target early instars of brown lacewing larvae (Neuroptera: Hemerobiidae). So far, five species were recognised from the Western Palaearctic region, of which four are reported from Northwestern Europe. In this study, we address the Northwestern European species diversity of the genus with an extended integrative taxonomy toolkit. A total of 700 specimens were examined for their external morphology, including the relevant type specimens. For 354 specimens, we obtained CO1 barcode sequences and applied three molecular species delimitation methods. All DNA barcode data are made publicly available via the German Barcode of Life (GBOL) and Barcode of Life Data system (BOLD) database. In addition, we examined images of Wing Interference Patterns (WIPs), examined the male genitalia and performed multivariate morphometric analyses. The analyses revealed two clusters which we describe as the immunis and eucharioides species groups based on differences in DNA barcode, external morphology, WIPs and size of the male genitalia. Furthermore, we complement the diagnosis of the genus Anacharis and describe three new species, Anacharis martinae Vogel, Forshage & Peters, sp. nov., Anacharis maxima Vogel, Forshage & Peters, sp. nov. and Anacharis minima Vogel, Forshage & Peters, sp. nov. Finally, we synonymise A. fergussoni Mata-Casanova & Pujade-Villar, 2018, syn. nov. with A. eucharioides (Dalman, 1818), and we reinstate A. ensifer Walker, 1835, stat. rev., A. typica Walker, 1835, stat. rev. and A. petiolata Zetterstedt, 1838, stat. rev. as valid species. In total, we recognise nine Northwestern European species to which we provide an identification key. The species of Anacharis are morphologically very variable. Morphometric analyses alone did not provide information sufficient to delimit species, neither did analyses of WIPs and male genitalia, with few notable exceptions. Analyses of molecular sequence data proved crucially helpful to reliably delimit species and to find morphological diagnostic characters in a reverse taxonomy approach. For delimiting species groups, all included analyses proved helpful, and we show that exploring an extended integrative taxonomy toolkit can be beneficial for a comprehensive characterisation of species. We acknowledge that a complete overview of species distributions, and characterisation of ecological niches & host records is still required to deeply understand the genus as a whole, yet our results already allow broad access to and inclusion of Anacharis species in downstream biodiversity research.

All native and many cultivated fig plants are pollinated by representatives of the family Agaonidae (fig wasps), which are specialised, secondarily phytophagous relatives of parasitoid wasps that evolved an obligate mutualism with fig trees. So far, distribution of Agaonidae in Europe has been limited to southern, mostly Mediterranean areas, for example, in Greece, Croatia, Hungary, Italy, France, Spain and Portugal. Here, we report the first four records of the family for Germany, all in the form of the widespread species Blastophaga psenes (Linnaeus, 1758). New verified records are from three States in western and south-western Germany, Baden-Wuerttemberg (Radolfzell at Lake Constance and Sasbach am Kaiserstuhl near Freiburg), Saarland (Saarbrücken) and Northrhine-Westalia (Bochum) and all are based on citizen-scientist observations and collections. The new records are considerably more northern than previously recorded localities and, strikingly, geographically distant from these. All records can be attributed to the presence of large male caprifig trees (Ficus carica L. var. caprificus), whose three generations of fruits host the development stages of Blastophaga psenes. We generated DNA barcode data of specimens from three localities and added them to the national GBOL (German Barcode of Life) database and the international Barcode of Life database (BOLD). The somewhat surprising occurrence of the species/family in Germany might be attributable to increasing temperatures as a result of global warming, but this needs further investigation. Additionally, the presence of fig wasps, assuming it stabilises, could offer new opportunities for fig farming in Germany.

DNA barcodes are a great tool for accelerated species identification and for complementing species delimitation. Furthermore, DNA barcode reference libraries are the decisive backbone feature for any metabarcoding study in biodiversity monitoring, conservation or ecology. However, in some taxa, DNA barcodes cannot be generated with published primers at a satisfying success rate and these groups will consequently be largely missing from any barcoding-based species list. Here, we provide a custom DNA barcoding forward primer for the Eurytomidae (Hymenoptera, Chalcidoidea), elevating the success rate of high-quality DNA barcodes from 33% to 88%. Eurytomidae is a severely understudied, taxonomically challenging, species-rich group of primarily parasitoid wasps. High species numbers, diverse ecological roles and widespread and common presence identify Eurytomidae as one of many crucial families in terrestrial ecosystems. It is now possible to include Eurytomidae when studying and monitoring the terrestrial fauna, highlighting that barcoding-based approaches will need to routinely use different primers to avoid biases in their data and inferences. The new DNA barcoding protocol is also a prerequisite for our integrative taxonomy study of the group, aiming at delimiting and characterising Central European species and filling the GBOL (German Barcode Of Life) DNA barcode reference library with species-named and voucher-linked sequences.

Abstract Species are the fundamental units of life and evolution. Their recognition is essential for science and society. Molecular methods have been increasingly used for the identification of animal species, despite several challenges. Here, we explore with genomic data from nine animal lineages a set of nuclear markers, namely metazoan‐level universal single‐copy orthologs (metazoan USCOs), for their use in species delimitation. Our data sets include arthropods and vertebrates. We use various data assembly strategies and use coalescent‐based species inference as well as population admixture analyses and phenetic methods. We demonstrate that metazoan USCOs distinguish well closely related morphospecies and consistently outperform classical mitochondrial DNA barcoding in discriminating closely related species in different animal taxa, as judged by comparison with morphospecies delimitations. USCOs overcome the general shortcomings of mitochondrial DNA barcodes, and due to standardization across Metazoa, also those of other approaches. They accurately assign samples not only to lower but also to higher taxonomic levels. Metazoan USCOs provide a powerful and unifying framework for DNA‐based species delimitation and taxonomy in animals and their employment could result in a more efficient use of research data and resources.

The family Pteromalidae (Hymenoptera: Chalcidoidea) is reviewed with the goal of providing nomenclatural changes and morphological diagnoses in preparation for a new molecular phylogeny and a book on world fauna that will contain keys to identification. Most subfamilies and some tribes of Pteromalidae are elevated to family level or transferred elsewhere in the superfamily. The resulting classification is a compromise, with the aim of preserving the validity and diagnosability of other, well-established families of Chalcidoidea. The following former subfamilies and tribes of Pteromalidae are elevated to family rank: Boucekiidae, Ceidae, Cerocephalidae, Chalcedectidae, Cleonymidae, Coelocybidae, Diparidae, Epichrysomallidae, Eunotidae, Herbertiidae, Hetreulophidae, Heydeniidae, Idioporidae, Lyciscidae, Macromesidae, Melanosomellidae, Moranilidae, Neodiparidae, Ooderidae, Pelecinellidae (senior synonym of Leptofoeninae), Pirenidae, Spalangiidae, and Systasidae. The following subfamilies are transferred from Pteromalidae: Chromeurytominae and Keiraninae to Megastigmidae, Elatoidinae to Neodiparidae, Nefoeninae to Pelecinellidae, and Erotolepsiinae to Spalangiidae. The subfamily Sycophaginae is transferred to Pteromalidae. The formerly incertae sedis tribe Lieparini is abolished and its single genus Liepara is transferred to Coelocybidae. The former tribe Tomocerodini is transferred to Moranilidae and elevated to subfamily status. The former synonym Tridyminae (Pirenidae) is treated as valid. The following former Pteromalidae are removed from the family and, due to phylogenetic uncertainty, placed as incertae sedis subfamilies or genera within Chalcidoidea: Austrosystasinae, Ditropinotellinae, Keryinae, Louriciinae, Micradelinae, Parasaphodinae, Rivasia, and Storeyinae. Within the remaining Pteromalidae, Miscogastrinae and Ormocerinae are confirmed as separate from Pteromalinae, the former tribe Trigonoderini is elevated to subfamily status, the former synonym Pachyneurinae is recognized as a distinct subfamily, and as the senior synonym of Austroterobiinae. The tribe Termolampini is synonymized under Pteromalini, and the tribe Uzkini is synonymized under Colotrechnini. Most former Otitesellinae, Sycoecinae, and Sycoryctinae are retained in the tribe Otitesellini, which is transferred to Pteromalinae, and all other genera of Pteromalinae are treated as Pteromalini. Eriaporidae is synonymized with Pirenidae, with Eriaporinae and Euryischiinae retained as subfamilies. Other nomenclatural acts performed here outside of Pteromalidae are as follows: Calesidae: elevation to family rank. Eulophidae: transfer of Boucekelimini and Platytetracampini to Opheliminae, and abolishment of the tribes Elasmini and Gyrolasomyiini. Baeomorphidae is recognized as the senior synonym of Rotoitidae. Khutelchalcididae is formally excluded from Chalcidoidea and placed as incertae sedis within Apocrita. Metapelmatidae and Neanastatidae are removed from Eupelmidae and treated as distinct families. Eopelma is removed from Eupelmidae and treated as an incertae sedis genus in Chalcidoidea. The following subfamilies and tribes are described as new: Cecidellinae (in Pirenidae), Enoggerinae (incertae sedis in Chalcidoidea), Erixestinae (in Pteromalidae), Eusandalinae (in Eupelmidae), Neapterolelapinae (incertae sedis in Chalcidoidea), Solenurinae (in Lyciscidae), Trisecodinae (in Systasidae), Diconocarini (in Pteromalidae: Miscogastrinae), and Trigonoderopsini (in Pteromalidae: Colotrechninae). A complete generic classification for discussed taxa is provided.

The number of currently described species of Afrotropical parasitoid wasps does not reflect the true species diversity. One of the most severely understudied parasitoid wasp groups is Ceraphronoidea. In this first study on Afrotropical mainland Ceraphronoidea in more than 20 years, which is also the first ever taxonomic monograph focusing on Ceraphronidae, we describe 88 new species of Ceraphronidae (85 new species) and Megaspilidae (3 new species) from Kakamega Forest (Kenya), Mt. Kilimanjaro (Tanzania) and Ivindo NP (Gabon): Aphanogmus abaluhya sp. nov., A. ashitakai sp. nov., A. idakho sp. nov., A. ikhongamurwi sp. nov., A. isiukhu sp. nov., A. kakamegaensis sp. nov., A. lateritorum sp. nov., A. mangimelii sp. nov., A. mariae sp. nov., A. mashariki sp. nov., A. nehbergi sp. nov., A. njia sp. nov., A. vestrii sp. nov., A. yala sp. nov. (all clavicornis species group), A. dimidiatus sp. nov., A. fraterculus sp. nov., A. guenteri sp. nov., A. kakakili sp. nov., A. kisiwa sp. nov., A. maua sp. nov., A. morriconei sp. nov., A. ndefu sp. nov., A. ngai sp. nov., A. nikii sp. nov., A. pilosicoxa sp. nov., A. rafikii sp. nov., A. robustus sp. nov., A. simbai sp. nov., A. taji sp. nov., A. ukanda sp. nov. (all fumipennis species group), A. campanula sp. nov., A. kikuyu sp. nov., A. pagoda sp. nov. (all tenuicornis species group), Ceraphron banda sp. nov., C. brashi sp. nov., C. breviharpis sp. nov., C. breviscapus sp. nov., C. buyangu sp. nov., C. chemositi sp. nov., C. cingulum sp. nov., C. clavatumeris sp. nov., C. digiti sp. nov., C. eaerendili sp. nov., C. ekero sp. nov., C. ellae sp. nov., C. eulbergi sp. nov., C. herreni sp. nov., C. hitagarciai sp. nov., C. insolitus sp. nov., C. isecheno sp. nov., C. isukha sp. nov., C. ivindoensis sp. nov., C. kaharabu sp. nov., C. kaimosiensis sp. nov., C. kakamegaensis sp. nov., C. kidole sp. nov., C. kimathii sp. nov., C. lirhanda sp. nov., C. longiharpis sp. nov., C. longisetae sp. nov., C. longumerunus sp. nov., C. maathaiae sp. nov., C. malava sp. nov., C. mamamutere sp. nov., C. metapleuralis sp. nov., C. mikoi sp. nov., C. mwekaensis sp. nov., C. nandi sp. nov., C. nzoia sp. nov., C. onesimusi sp. nov., C. pilosiharpis sp. nov., C. pleurosulcus sp. nov., C. reinholdi sp. nov., C. salazar sp. nov., C. sataoi sp. nov., C. semira sp. nov., C. sungura sp. nov., C. tenuimeris sp. nov., C. tiriki sp. nov., C. trietschae sp. nov., Cyoceraphron dhahabudorsalis sp. nov., C. harpe sp. nov., C. invisibilis sp. nov., C. kahawia sp. nov., C. njano sp. nov. (all Ceraphronidae), Conostigmus kijiko sp. nov., C. koleo sp. nov., and Dendrocerus wachagga sp. nov. (all Megaspilidae). In addition, we describe four species of Aphanogmus and five species of Ceraphron without formal naming. A neotype is designated for Dendrocerus anneckei Dessart, 1985 (Megaspilidae). With these new species we more than double the number described from the Afrotropical mainland (65 vs 153). The species numbers found allow us to estimate the real worldwide species number of Ceraphronoidea as being roughly 12 000–21 000, i.e., 16–29 times the number of the currently described species (~730, including the species described herein). This study is meant to highlight that it is necessary and also possible to study the parasitoid wasps of tropical regions and provide momentum for exploring the diversity of small and diverse insect groups in the Afrotropics and elsewhere while also providing the basic knowledge that is much needed for protecting biodiversity and understanding evolution and the networks of life on earth. All described species are diagnosed and illustrated, with focus on the male genitalia. Furthermore, we provide an identification key to males of Afrotropical Ceraphronidae.