Hannes Baur
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
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Research Interests
Hannes Baur has a total of 126 co-authors. Here are the top co-authors by number of shared publications:
Armin Coray
4 shared publications- Ekaterina V. Tselikh
Zoological Institute; Russian Academy of Sciences; St Petersburg; 199034; Russia
4 shared publications - Jean-Yves Rasplus
CBGP; INRAE; CIRAD; IRD; Montpellier SupAgro; University of Montpellier; Montpellier; France
4 shared publications - Lars Krogmann
State Museum of Natural History Stuttgart Stuttgart Germany
4 shared publications - Oliver Niehuis
Department of Evolutionary Biology and Ecology, Institute of Biology I (Zoology) University of Freiburg Freiburg Germany
4 shared publications - Ralph S. Peters
Leibniz Institute for the Analysis of Biodiversity Change, Museum Koenig, Bonn, Germany
4 shared publications
Latest Publications
- Open Access
- 4 September 2025
- Published by Pensoft Publishers in ZooKeys
- Vol. 1251, 97-114
Review of the sequester group of Pteromalus Swederus, 1795 (Hymenoptera, Pteromalidae) with description of three new species
Palaearctic species of the sequester group of Pteromalus Swederus, 1795 are reviewed. Three new species, P. boleensis Yan, Li & Tselikh, sp. nov. (Kazakhstan, China), P. longipedicellus Yan, Li & Tselikh, sp. nov. (China) and P. oscolensis Tselikh, sp. nov. (Russia, China) are described and illustrated. Types of P. cionobia (Erdös, 1953) and P. sequester Walker, 1835 are redescribed. An identification key to females of the sequester group of Pteromalus is given.
- 4 September 2025
- Published by Pensoft Publishers in ZooKeys
- Vol. 1251, 97-114
Open AccessReview of the sequester group of Pteromalus Swederus, 1795 (Hymenoptera, Pteromalidae) with description of three new species
Palaearctic species of the sequester group of Pteromalus Swederus, 1795 are reviewed. Three new species, P. boleensis Yan, Li & Tselikh, sp. nov. (Kazakhstan, China), P. longipedicellus Yan, Li & Tselikh, sp. nov. (China) and P. oscolensis Tselikh, sp. nov. (Russia, China) are described and illustrated. Types of P. cionobia (Erdös, 1953) and P. sequester Walker, 1835 are redescribed. An identification key to females of the sequester group of Pteromalus is given.
- 28 February 2025
- Published by CABI Publishing
- p. 789-795
Morphometric Methods for Species Recognition
- Open Access
- 30 August 2024
- Published by Magnolia Press in Zootaxa
- Vol. 5501 (2) , 201-236
The species of Pteromalus Swederus in America north of Mexico with a 4:4 mandibular formula, and description of a potential biocontrol agent of the introduced pest Anthonomus rubi (Herbst) (Coleoptera: Curculionidae)
The strawberry blossom weevil, Anthonomus rubi (Herbst) (Coleoptera: Curculionidae), is native to Europe, Asia, and parts of North Africa, and has recently established in British Columbia, Canada and Washington State, USA. To determine whether any parasitoids in British Columbia parasitize this recently-established pest, A. rubi-infested buds of Rosaceous host plants were collected and reared for parasitoid emergence. Pteromalus quadridentatus Gibson n. sp. (Hymenoptera: Chalcidoidea: Pteromalidae) is described from both sexes reared as solitary ectoparasitoids of A. rubi. Males and females are partly characterized by both mandibles having four teeth (4:4 mandibular formula), which is known for only four of the other previously recorded 39 extant species of Pteromalus from the Nearctic region—P. apum (Retzius), P. cassotis Walker, P. hemileucae Gahan, and P. puparum (L.). The species of Pteromalus recorded from the Nearctic region are listed along with notes on their known mandibular dentition or other features that differentiate them from P. quadridentatus. The five species with a 4:4 mandibular formula are keyed, diagnosed and illustrated through macrophotography. Additionally, both sexes of P. quadridentatus are described more comprehensively, including variation in structure, colour and sculpture correlated with body size; the morphological species limits of P. cassotis are also discussed. Species of Pteromalus with a 4:4 mandibular formula from other regions where A. rubi is recorded are also listed and discussed, but only sufficiently to exclude them as potentially conspecific with P. quadridentatus. A phylogenetic tree constructed using Maximum Likelihood based on COI barcode sequences showed strong support for P. quadridentatus being monophyletic and sister to P. bedeguaris (Thomson). Pteromalus quadridentatus is the first parasitoid recorded from A. rubi in its invaded range, although it is still uncertain whether this parasitoid is native to North America or was introduced along with A. rubi or another host species.
- 30 August 2024
- Published by Magnolia Press in Zootaxa
- Vol. 5501 (2) , 201-236
Open AccessThe species of Pteromalus Swederus in America north of Mexico with a 4:4 mandibular formula, and description of a potential biocontrol agent of the introduced pest Anthonomus rubi (Herbst) (Coleoptera: Curculionidae)
The strawberry blossom weevil, Anthonomus rubi (Herbst) (Coleoptera: Curculionidae), is native to Europe, Asia, and parts of North Africa, and has recently established in British Columbia, Canada and Washington State, USA. To determine whether any parasitoids in British Columbia parasitize this recently-established pest, A. rubi-infested buds of Rosaceous host plants were collected and reared for parasitoid emergence. Pteromalus quadridentatus Gibson n. sp. (Hymenoptera: Chalcidoidea: Pteromalidae) is described from both sexes reared as solitary ectoparasitoids of A. rubi. Males and females are partly characterized by both mandibles having four teeth (4:4 mandibular formula), which is known for only four of the other previously recorded 39 extant species of Pteromalus from the Nearctic region—P. apum (Retzius), P. cassotis Walker, P. hemileucae Gahan, and P. puparum (L.). The species of Pteromalus recorded from the Nearctic region are listed along with notes on their known mandibular dentition or other features that differentiate them from P. quadridentatus. The five species with a 4:4 mandibular formula are keyed, diagnosed and illustrated through macrophotography. Additionally, both sexes of P. quadridentatus are described more comprehensively, including variation in structure, colour and sculpture correlated with body size; the morphological species limits of P. cassotis are also discussed. Species of Pteromalus with a 4:4 mandibular formula from other regions where A. rubi is recorded are also listed and discussed, but only sufficiently to exclude them as potentially conspecific with P. quadridentatus. A phylogenetic tree constructed using Maximum Likelihood based on COI barcode sequences showed strong support for P. quadridentatus being monophyletic and sister to P. bedeguaris (Thomson). Pteromalus quadridentatus is the first parasitoid recorded from A. rubi in its invaded range, although it is still uncertain whether this parasitoid is native to North America or was introduced along with A. rubi or another host species.
- Open Access
- 26 June 2024
- Published by Pensoft Publishers in ZooKeys
- Vol. 1205 (1205) , 223-238
Genetic identification, morphology and distribution of Natrix helvetica subspecies in southern and western Switzerland (Reptilia, Squamata, Serpentes)
Most of Switzerland is inhabited by the nominotypical subspecies of the barred grass snake (Natrix helvetica helvetica), which is characterized by mitochondrial DNA lineage E. Only in the northeast of the country, the common grass snake (N. natrix) occurs and hybridizes with N. h. helvetica in a narrow contact zone. However, we discovered that in southern and western Switzerland barred grass snakes representing another mtDNA lineage (lineage C) are widely distributed. Lineage C is typical for Alpine populations of the southern subspecies N. h. sicula. Our microsatellite analyses of the Swiss samples revealed differences between the two subspecies and also a substructure with two clusters in each subspecies. Furthermore, we discovered a contact and hybrid zone of N. h. helvetica and N. h. sicula along the northern shore of Lake Geneva and also confirm that interbreeding with alien common grass snakes (N. n. moreotica, mtDNA lineage 7) occurs there. This finding is of concern for nature conservation and measures should be taken to prevent further genetic pollution. Using morphometrics, we found no differences between the two subspecies of N. helvetica, while N. natrix was slightly distinct from N. helvetica.
- 26 June 2024
- Published by Pensoft Publishers in ZooKeys
- Vol. 1205 (1205) , 223-238
Open AccessGenetic identification, morphology and distribution of Natrix helvetica subspecies in southern and western Switzerland (Reptilia, Squamata, Serpentes)
Most of Switzerland is inhabited by the nominotypical subspecies of the barred grass snake (Natrix helvetica helvetica), which is characterized by mitochondrial DNA lineage E. Only in the northeast of the country, the common grass snake (N. natrix) occurs and hybridizes with N. h. helvetica in a narrow contact zone. However, we discovered that in southern and western Switzerland barred grass snakes representing another mtDNA lineage (lineage C) are widely distributed. Lineage C is typical for Alpine populations of the southern subspecies N. h. sicula. Our microsatellite analyses of the Swiss samples revealed differences between the two subspecies and also a substructure with two clusters in each subspecies. Furthermore, we discovered a contact and hybrid zone of N. h. helvetica and N. h. sicula along the northern shore of Lake Geneva and also confirm that interbreeding with alien common grass snakes (N. n. moreotica, mtDNA lineage 7) occurs there. This finding is of concern for nature conservation and measures should be taken to prevent further genetic pollution. Using morphometrics, we found no differences between the two subspecies of N. helvetica, while N. natrix was slightly distinct from N. helvetica.
- Top Cited PapersOpen Access
- 2 November 2023
- Published by Wiley in Cladistics
- Vol. 40 (1) , 34-63
The Chalcidoidea bush of life: evolutionary history of a massive radiation of minute wasps
Chalcidoidea are mostly parasitoid wasps that include as many as 500 000 estimated species. Capturing phylogenetic signal from such a massive radiation can be daunting. Chalcidoidea is an excellent example of a hyperdiverse group that has remained recalcitrant to phylogenetic resolution. We combined 1007 exons obtained with Anchored Hybrid Enrichment with 1048 ultra‐conserved elements (UCEs) for 433 taxa including all extant families, >95% of all subfamilies, and 356 genera chosen to represent the vast diversity of the superfamily. Going back and forth between the molecular results and our collective knowledge of morphology and biology, we detected bias in the analyses that was driven by the saturation of nucleotide data. Our final results are based on a concatenated analysis of the least saturated exons and UCE datasets (2054 loci, 284 106 sites). Our analyses support an expected sister relationship with Mymarommatoidea. Seven previously recognized families were not monophyletic, so support for a new classification is discussed. Natural history in some cases would appear to be more informative than morphology, as illustrated by the elucidation of a clade of plant gall associates and a clade of taxa with planidial first‐instar larvae. The phylogeny suggests a transition from smaller soft‐bodied wasps to larger and more heavily sclerotized wasps, with egg parasitism as potentially ancestral for the entire superfamily. Deep divergences in Chalcidoidea coincide with an increase in insect families in the fossil record, and an early shift to phytophagy corresponds with the beginning of the “Angiosperm Terrestrial Revolution”. Our dating analyses suggest a middle Jurassic origin of 174 Ma (167.3–180.5 Ma) and a crown age of 162.2 Ma (153.9–169.8 Ma) for Chalcidoidea. During the Cretaceous, Chalcidoidea may have undergone a rapid radiation in southern Gondwana with subsequent dispersals to the Northern Hemisphere. This scenario is discussed with regard to knowledge about the host taxa of chalcid wasps, their fossil record and Earth's palaeogeographic history.
- 2 November 2023
- Published by Wiley in Cladistics
- Vol. 40 (1) , 34-63
Top Cited PapersOpen AccessThe Chalcidoidea bush of life: evolutionary history of a massive radiation of minute wasps
Chalcidoidea are mostly parasitoid wasps that include as many as 500 000 estimated species. Capturing phylogenetic signal from such a massive radiation can be daunting. Chalcidoidea is an excellent example of a hyperdiverse group that has remained recalcitrant to phylogenetic resolution. We combined 1007 exons obtained with Anchored Hybrid Enrichment with 1048 ultra‐conserved elements (UCEs) for 433 taxa including all extant families, >95% of all subfamilies, and 356 genera chosen to represent the vast diversity of the superfamily. Going back and forth between the molecular results and our collective knowledge of morphology and biology, we detected bias in the analyses that was driven by the saturation of nucleotide data. Our final results are based on a concatenated analysis of the least saturated exons and UCE datasets (2054 loci, 284 106 sites). Our analyses support an expected sister relationship with Mymarommatoidea. Seven previously recognized families were not monophyletic, so support for a new classification is discussed. Natural history in some cases would appear to be more informative than morphology, as illustrated by the elucidation of a clade of plant gall associates and a clade of taxa with planidial first‐instar larvae. The phylogeny suggests a transition from smaller soft‐bodied wasps to larger and more heavily sclerotized wasps, with egg parasitism as potentially ancestral for the entire superfamily. Deep divergences in Chalcidoidea coincide with an increase in insect families in the fossil record, and an early shift to phytophagy corresponds with the beginning of the “Angiosperm Terrestrial Revolution”. Our dating analyses suggest a middle Jurassic origin of 174 Ma (167.3–180.5 Ma) and a crown age of 162.2 Ma (153.9–169.8 Ma) for Chalcidoidea. During the Cretaceous, Chalcidoidea may have undergone a rapid radiation in southern Gondwana with subsequent dispersals to the Northern Hemisphere. This scenario is discussed with regard to knowledge about the host taxa of chalcid wasps, their fossil record and Earth's palaeogeographic history.
- Top Cited PapersOpen Access
- 20 December 2022
- Published by Pensoft Publishers in Journal of Hymenoptera Research
- Vol. 94, 13-88
From hell’s heart I stab at thee! A determined approach towards a monophyletic Pteromalidae and reclassification of Chalcidoidea (Hymenoptera)
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.
- 20 December 2022
- Published by Pensoft Publishers in Journal of Hymenoptera Research
- Vol. 94, 13-88
Top Cited PapersOpen AccessFrom hell’s heart I stab at thee! A determined approach towards a monophyletic Pteromalidae and reclassification of Chalcidoidea (Hymenoptera)
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.
- Open Access
The Chalcidoidea bush of life – a massive radiation blurred by mutational saturation
Capturing phylogenetic signal from a massive radiation can be daunting. The superfamily Chalcidoidea is an excellent example of a hyperdiverse group that has remained recalcitrant to phylogenetic resolution. Chalcidoidea are mostly parasitoid wasps that until now included 27 families, 87 subfamilies and as many as 500,000 estimated species. We combined 1007 exons obtained with Anchored Hybrid Enrichment with 1048 Ultra-Conserved Elements (UCEs) for 433 taxa including all extant families, over 95% of all subfamilies and 356 genera chosen to represent the vast diversity of the superfamily. Going back and forth between molecular results and our collective morphological and biological knowledge, we detected insidious bias driven by the saturation of nucleotide data and highlighted morphological convergences. Our final results are based on a concatenated analysis of the least saturated exons and UCE data sets (2054 loci, 284,106 sites). Our analyses support a sister relationship with Mymarommatoidea. Seven of the previously recognized families were not monophyletic, so foundations for a new classification are discussed. Biology appears potentially more informative than morphology, as illustrated by the elucidation of a clade of plant gall associates and a clade of taxa with planidial first-instar larvae. The phylogeny suggests a shift from smaller soft-bodied wasps to larger and more heavily sclerotized wasps. Deep divergences in Chalcidoidea coincide with an increase in insect families in the fossil record, and an early shift to phytophagy corresponds with the beginning of the “Angiosperm Terrestrial Revolution”. Our dating analyses suggest a Middle Jurassic origin of 174 Ma (167.3-180.5 Ma) and a crown age of 162.2 Ma (153.9–169.8 Ma) for Chalcidoidea. During the Cretaceous, Chalcidoidea underwent a rapid radiation in southern Gondwana with subsequent dispersals to the Northern Hemisphere. This scenario is discussed with regard to knowledge about host taxa of chalcid wasps, their fossil record, and Earth’s paleogeographic history.
Open AccessThe Chalcidoidea bush of life – a massive radiation blurred by mutational saturation
Capturing phylogenetic signal from a massive radiation can be daunting. The superfamily Chalcidoidea is an excellent example of a hyperdiverse group that has remained recalcitrant to phylogenetic resolution. Chalcidoidea are mostly parasitoid wasps that until now included 27 families, 87 subfamilies and as many as 500,000 estimated species. We combined 1007 exons obtained with Anchored Hybrid Enrichment with 1048 Ultra-Conserved Elements (UCEs) for 433 taxa including all extant families, over 95% of all subfamilies and 356 genera chosen to represent the vast diversity of the superfamily. Going back and forth between molecular results and our collective morphological and biological knowledge, we detected insidious bias driven by the saturation of nucleotide data and highlighted morphological convergences. Our final results are based on a concatenated analysis of the least saturated exons and UCE data sets (2054 loci, 284,106 sites). Our analyses support a sister relationship with Mymarommatoidea. Seven of the previously recognized families were not monophyletic, so foundations for a new classification are discussed. Biology appears potentially more informative than morphology, as illustrated by the elucidation of a clade of plant gall associates and a clade of taxa with planidial first-instar larvae. The phylogeny suggests a shift from smaller soft-bodied wasps to larger and more heavily sclerotized wasps. Deep divergences in Chalcidoidea coincide with an increase in insect families in the fossil record, and an early shift to phytophagy corresponds with the beginning of the “Angiosperm Terrestrial Revolution”. Our dating analyses suggest a Middle Jurassic origin of 174 Ma (167.3-180.5 Ma) and a crown age of 162.2 Ma (153.9–169.8 Ma) for Chalcidoidea. During the Cretaceous, Chalcidoidea underwent a rapid radiation in southern Gondwana with subsequent dispersals to the Northern Hemisphere. This scenario is discussed with regard to knowledge about host taxa of chalcid wasps, their fossil record, and Earth’s paleogeographic history.
- Open Access
- 12 May 2022
- Published by Academy of Science of South Africa in African Entomology
- Vol. 30
Identity of wasp parasitoids (Hymenoptera) attacking Pieris brassicae (Linnaeus, 1758) (Lepidoptera: Pieridae) in South Africa
The alien invasive large cabbage white, Pieris brassicae (Linnaeus, 1758) (Pieridae), although introduced into South Africa more than 27 years ago, has not dramatically expanded its distribution, possibly because it is effectively attacked by two parasitoid wasp species. Even though there is a cohort of parasitoid species associated with P. brassicae in the Northern Hemisphere, these are the only two recorded parasitoids in South Africa. We determine these parasitoid wasps as Cotesia glomerata (Linnaeus, 1758) (Braconidae: Microgastrinae) and Pteromalus puparum (Linnaeus, 1758) (Pteromalidae), and provide high resolution images and DNA barcodes to facilitate their recognition. This is the first record of C. glomerata from the Afrotropical region.
- 12 May 2022
- Published by Academy of Science of South Africa in African Entomology
- Vol. 30
Open AccessIdentity of wasp parasitoids (Hymenoptera) attacking Pieris brassicae (Linnaeus, 1758) (Lepidoptera: Pieridae) in South Africa
The alien invasive large cabbage white, Pieris brassicae (Linnaeus, 1758) (Pieridae), although introduced into South Africa more than 27 years ago, has not dramatically expanded its distribution, possibly because it is effectively attacked by two parasitoid wasp species. Even though there is a cohort of parasitoid species associated with P. brassicae in the Northern Hemisphere, these are the only two recorded parasitoids in South Africa. We determine these parasitoid wasps as Cotesia glomerata (Linnaeus, 1758) (Braconidae: Microgastrinae) and Pteromalus puparum (Linnaeus, 1758) (Pteromalidae), and provide high resolution images and DNA barcodes to facilitate their recognition. This is the first record of C. glomerata from the Afrotropical region.
- Open Access
- 17 December 2021
- Published by Pensoft Publishers in ZooKeys
- Vol. 1078 (1078) , 107-134
Incongruent molecular and morphological variation in the crab spider Synema globosum (Araneae, Thomisidae) in Europe
Establishing species boundaries is one of the challenges taxonomists around the world have been tackling for centuries. The relation between intraspecific and interspecific variability is still under discussion and in many taxa it remains understudied. Here the hypothesis of single versus multiple species of the crab spider Synema globosum (Fabricius) is tested. The wide distribution range as well as its high morphological variability makes this species an interesting candidate for re-evaluation using an integrative approach. This study combines information from barcoding, phylogenetic reconstruction based on mitochondrial CO1 and ITS2 of more than 60 specimens collected over a wide range of European localities, and morphology. The findings show deep clades with up to 6% mean pairwise distance in the CO1 barcode without any biogeographical pattern. The nuclear ITS2 gene did not support the CO1 clades. Morphological assessment of somatic and genital characters in males and females and a morphometric analysis of the male palp uncovered high intraspecific variation that does not match the CO1 or ITS2 phylogenies or biogeography either. Screening for endosymbiotic Wolbachia bacteria was conducted and only a single infected specimen was found. Several scenarios might explain these inconsistent patterns. While the deep divergences in the barcoding marker might suggest cryptic or ongoing speciation or geographical isolation in the past, the lack of congruent variation in the nuclear ITS2 gene or the studied morphological character systems, especially the male palp, indicates that S. globosum might simply be highly polymorphic both in terms of its mtDNA and morphology. Therefore, more data on ecology and behaviour and full genome sequences are necessary to ultimately resolve this taxonomically intriguing case.
- 17 December 2021
- Published by Pensoft Publishers in ZooKeys
- Vol. 1078 (1078) , 107-134
Open AccessIncongruent molecular and morphological variation in the crab spider Synema globosum (Araneae, Thomisidae) in Europe
Establishing species boundaries is one of the challenges taxonomists around the world have been tackling for centuries. The relation between intraspecific and interspecific variability is still under discussion and in many taxa it remains understudied. Here the hypothesis of single versus multiple species of the crab spider Synema globosum (Fabricius) is tested. The wide distribution range as well as its high morphological variability makes this species an interesting candidate for re-evaluation using an integrative approach. This study combines information from barcoding, phylogenetic reconstruction based on mitochondrial CO1 and ITS2 of more than 60 specimens collected over a wide range of European localities, and morphology. The findings show deep clades with up to 6% mean pairwise distance in the CO1 barcode without any biogeographical pattern. The nuclear ITS2 gene did not support the CO1 clades. Morphological assessment of somatic and genital characters in males and females and a morphometric analysis of the male palp uncovered high intraspecific variation that does not match the CO1 or ITS2 phylogenies or biogeography either. Screening for endosymbiotic Wolbachia bacteria was conducted and only a single infected specimen was found. Several scenarios might explain these inconsistent patterns. While the deep divergences in the barcoding marker might suggest cryptic or ongoing speciation or geographical isolation in the past, the lack of congruent variation in the nuclear ITS2 gene or the studied morphological character systems, especially the male palp, indicates that S. globosum might simply be highly polymorphic both in terms of its mtDNA and morphology. Therefore, more data on ecology and behaviour and full genome sequences are necessary to ultimately resolve this taxonomically intriguing case.
- Open Access
- 7 December 2021
- Published by Pensoft Publishers in Biodiversity Data Journal
- Vol. 9, e77092
Tiny wasps, huge diversity – A review of German Pteromalidae with new generic and species records (Hymenoptera: Chalcidoidea)
Despite their ecological and economic importance, hymenopteran parasitoids are severely understudied. Even in countries with a long taxonomic history such as Germany, dating back to the 18th century and including prolific figures like Christian Gottfired Nees von Esenbeck and Otto Schmiedeknecht, those species-rich groups are seldom the subject of comprehensive research efforts, leaving their true diversity unknown. This is often due to their small size of a few millimetres on average, leading to difficulties in their identification and examination. The chalcidoid family Pteromalidae is no exception to this neglect. So far, 735 species have been reported from Germany. Estimating the diversity of this group is not possible, but it has to be assumed that many more species are still to be discovered in Germany.With this study, we improve the knowledge on pteromalid diversity and present new records of 17 genera and 41 species, previously unknown to occur in Germany. We also match and describe previously unknown sexes of two species, based on DNA barcode data. The results of this study were generated as part of the German Barcode of Life Project. The newly-recorded species are illustrated and notes on the biology and distribution are given. The ecological significance of Pteromalidae and potential value as indicators for nature conservation efforts are briefly discussed.
- 7 December 2021
- Published by Pensoft Publishers in Biodiversity Data Journal
- Vol. 9, e77092
Open AccessTiny wasps, huge diversity – A review of German Pteromalidae with new generic and species records (Hymenoptera: Chalcidoidea)
Despite their ecological and economic importance, hymenopteran parasitoids are severely understudied. Even in countries with a long taxonomic history such as Germany, dating back to the 18th century and including prolific figures like Christian Gottfired Nees von Esenbeck and Otto Schmiedeknecht, those species-rich groups are seldom the subject of comprehensive research efforts, leaving their true diversity unknown. This is often due to their small size of a few millimetres on average, leading to difficulties in their identification and examination. The chalcidoid family Pteromalidae is no exception to this neglect. So far, 735 species have been reported from Germany. Estimating the diversity of this group is not possible, but it has to be assumed that many more species are still to be discovered in Germany.With this study, we improve the knowledge on pteromalid diversity and present new records of 17 genera and 41 species, previously unknown to occur in Germany. We also match and describe previously unknown sexes of two species, based on DNA barcode data. The results of this study were generated as part of the German Barcode of Life Project. The newly-recorded species are illustrated and notes on the biology and distribution are given. The ecological significance of Pteromalidae and potential value as indicators for nature conservation efforts are briefly discussed.