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Figure 1 from: Simutnik SA, Perkovsky EE, Vasilenko DV (2020) First record of Leptoomus janzeni Gibson (Hymenoptera, Chalcidoidea) from Rovno amber. Journal of Hymenoptera Research 80: 137-145. https://doi.org/10.3897/jhr.80.58882
Figure 1 Leptoomus janzeni, female VT-95 from Rovno amber (deposed in SIZK) A piece of amber containing the specimen B habitus ventrolateral (left side) C habitus dorsolateral (right side) D head and mesosoma dorsolateral, dorsellum E antenna ventral F antenna dorsal G head frontolateroventral, part of antenna with mps arrowed H forewing I protibial spur, protarsus J mesotibial spur, mesotarsus.
Figure 6 from: Peris-Felipo FJ, Stigenberg J, Quicke DLJ, Belokobylskij SA (2020) Revision of Neorthostigma Belokobylskij, 1998 (Hymenoptera, Braconidae, Alysiinae) with description of a new species from Papua New Guinea. Journal of Hymenoptera Research 80: 31-47. https://doi.org/10.3897/jhr.80.58737
Figure 6 Neorthostigma macrops (Stelfox & Graham, 1951) (A–F: female, holotype of Neorthostigma eoum) A head, frontal view B head and mesonotum, dorsal view C propodeum, dorsal view D first metasomal tergite, dorsal view E hind leg, metasoma and ovipositor, lateral view F fore and hind wings.
Figure 5 from: Peris-Felipo FJ, Stigenberg J, Quicke DLJ, Belokobylskij SA (2020) Revision of Neorthostigma Belokobylskij, 1998 (Hymenoptera, Braconidae, Alysiinae) with description of a new species from Papua New Guinea. Journal of Hymenoptera Research 80: 31-47. https://doi.org/10.3897/jhr.80.58737
Figure 5 Neorthostigma macrops (Stelfox & Graham, 1951) (A, B female, holotype of A. macrops; C–F female, holotype of Neorthostigma eoum) A, C habitus, lateral view B habitus, dorsal view D head and mesosoma, lateral view E mandible F antenna.
Figure 4 from: Peris-Felipo FJ, Stigenberg J, Quicke DLJ, Belokobylskij SA (2020) Revision of Neorthostigma Belokobylskij, 1998 (Hymenoptera, Braconidae, Alysiinae) with description of a new species from Papua New Guinea. Journal of Hymenoptera Research 80: 31-47. https://doi.org/10.3897/jhr.80.58737
Figure 4 Neorthostigma braeti Peris-Felipo, sp. nov. (female, holotype) A propodeum, dorsal view B first metasomal tergite, dorsal view C hind leg, metasoma and ovipositor, lateral view D fore and hind wings.
Figure 3 from: Peris-Felipo FJ, Stigenberg J, Quicke DLJ, Belokobylskij SA (2020) Revision of Neorthostigma Belokobylskij, 1998 (Hymenoptera, Braconidae, Alysiinae) with description of a new species from Papua New Guinea. Journal of Hymenoptera Research 80: 31-47. https://doi.org/10.3897/jhr.80.58737
Figure 3 Neorthostigma braeti Peris-Felipo, sp. nov. (female, holotype) A habitus, lateral view B head and mesosoma, lateral view C mandible D antenna E head, frontal view F head and mesonotum, dorsal view.
Figure 7 from: Peris-Felipo FJ, Stigenberg J, Quicke DLJ, Belokobylskij SA (2020) Revision of Neorthostigma Belokobylskij, 1998 (Hymenoptera, Braconidae, Alysiinae) with description of a new species from Papua New Guinea. Journal of Hymenoptera Research 80: 31-47. https://doi.org/10.3897/jhr.80.58737
Figure 7 Propodeum variation of Neorthostigma macrops (Stelfox & Graham, 1951) (A female, holotype of Neorthostigma eoum; B–D additional material).
Figure 2 from: Peris-Felipo FJ, Stigenberg J, Quicke DLJ, Belokobylskij SA (2020) Revision of Neorthostigma Belokobylskij, 1998 (Hymenoptera, Braconidae, Alysiinae) with description of a new species from Papua New Guinea. Journal of Hymenoptera Research 80: 31-47. https://doi.org/10.3897/jhr.80.58737
Figure 2 Neorthostigma brachyclypeata (Fischer, 1978) (female, holotype) A propodeum, dorsal view B first metasomal tergite, dorsal view C hind leg, metasoma and ovipositor, lateral view D fore and hind wings.
Figures 8-11 from: Ganjisaffar F, Talamas EJ, Bon MC, Perring TM (2020) First report and integrated analysis of two native Trissolcus species utilizing Bagrada hilaris eggs in California. Journal of Hymenoptera Research 80: 49-70. https://doi.org/10.3897/jhr.80.57024
Figures 8-11 Trissolcus utahensis, head, anterior view 8 DPI_FSCA00033239 (ex. B. hilaris) 9 FSCA 00033041 (ex. P. maculiventris) 10 FSCA 00000302 (ex. P. maculiventris) 11 FSCA 00033040 (Ex. P. maculiventris). Scale bars in millimeters.
Figure 3 from: Ganjisaffar F, Talamas EJ, Bon MC, Perring TM (2020) First report and integrated analysis of two native Trissolcus species utilizing Bagrada hilaris eggs in California. Journal of Hymenoptera Research 80: 49-70. https://doi.org/10.3897/jhr.80.57024
Figure 3 TCS COI haplotype network for the four clades of T. utahensis by fixing connection limits at 50 steps. Each haplotype is represented by a colored circle. Lines represent one mutational step between haplotypes, and dark circles represent unsampled haplotypes inferred from the data. Interrupted lines were used when haplotypes were separated by a long branch of more than 7 mutation steps.
Figures 23-25 from: Ganjisaffar F, Talamas EJ, Bon MC, Perring TM (2020) First report and integrated analysis of two native Trissolcus species utilizing Bagrada hilaris eggs in California. Journal of Hymenoptera Research 80: 49-70. https://doi.org/10.3897/jhr.80.57024
Figures 23-25 Trissolcus utahensis (FSCA 00091872, ex. B. hilaris) 23 head, anterior view 24 lateral habitus 25 head, mesosoma, metasoma, dorsal view. Scale bars in millimeters.
Figure 4 from: Werneck HA, Campos LAO (2020) A study of the biology of Epicharis (Epicharoides) picta using emergence-traps. Journal of Hymenoptera Research 80: 147-167. https://doi.org/10.3897/jhr.80.56898
Figure 4 Brood cells of Epicharis (Epicharoides) pictaA outer cell wall surface B mature larva inside the cell C inner cell wall surface D the cell cap inserted below the apex of the cell wall E variation in brood cell shape. Scale bars: 5 mm.
Figure 1 from: Peris-Felipo FJ, Stigenberg J, Quicke DLJ, Belokobylskij SA (2020) Revision of Neorthostigma Belokobylskij, 1998 (Hymenoptera, Braconidae, Alysiinae) with description of a new species from Papua New Guinea. Journal of Hymenoptera Research 80: 31-47. https://doi.org/10.3897/jhr.80.58737
Figure 1 Neorthostigma brachyclypeata (Fischer, 1978) (female, holotype) A habitus, lateral view B head and mesosoma, lateral view C mandible D antenna E head, frontal view F head and mesonotum, dorsal view.
Figure 2 from: Ganjisaffar F, Talamas EJ, Bon MC, Perring TM (2020) First report and integrated analysis of two native Trissolcus species utilizing Bagrada hilaris eggs in California. Journal of Hymenoptera Research 80: 49-70. https://doi.org/10.3897/jhr.80.57024
Figure 2 The Bayesian 50% majority rule consensus tree inferred from the 56 CO1 sequences of the six Trissolcus species including T. hullensis and T. utahensis. Only posterior probabilities >90% are indicated on the nodes. The tree is rooted with the outgroup Trissolcus thyantae (GenBank MN615574). The scale bar corresponds to 0.1 estimated substitutions per site.
Figure 3 from: Werneck HA, Campos LAO (2020) A study of the biology of Epicharis (Epicharoides) picta using emergence-traps. Journal of Hymenoptera Research 80: 147-167. https://doi.org/10.3897/jhr.80.56898
Figure 3 Nesting habits and nest architecture of Epicharis (Epicharoides) pictaA female resting inside the nests at night B female of E. picta excavating nest C, D entrance of the nests showing the presence of a tumulus E, F architecture of 110 cm deep nests.
Figure 1 from: Werneck HA, Campos LAO (2020) A study of the biology of Epicharis (Epicharoides) picta using emergence-traps. Journal of Hymenoptera Research 80: 147-167. https://doi.org/10.3897/jhr.80.56898
Figure 1 Climatological data from Viçosa, Minas Gerais-Brazil, between 2009 and 2011 (Source: Estação Climatológica Principal de Viçosa, Departamento de Engenharia Agrícola – UFV).
Figure 2 from: Werneck HA, Campos LAO (2020) A study of the biology of Epicharis (Epicharoides) picta using emergence-traps. Journal of Hymenoptera Research 80: 147-167. https://doi.org/10.3897/jhr.80.56898
Figure 2 Emergence-traps set up on aggregate of Epicharis (Epicharoides) picta (A); Detail of emergence-trap (B).
Figure 6 from: Werneck HA, Campos LAO (2020) A study of the biology of Epicharis (Epicharoides) picta using emergence-traps. Journal of Hymenoptera Research 80: 147-167. https://doi.org/10.3897/jhr.80.56898
Figure 6 Natural enemies and associated species of Epicharis (Epicharoides) pictaARhathymus friesei inspecting at the nest aggregation BTetraonyx sexguttata emerging from a nest of E. pictaCApiomerus lanipes preying on a female of E. pictaDTraumatomutilla sp. inspecting the entrance of a nest of E. picta.
Figure 8 from: Komeda Y, Mita T, Hirose Y, Yamagishi K (2020) Taxonomic revision of charon-, floridanum- and muscaeforme-groups of Gryon Haliday, 1833 (Hymenoptera, Scelionidae) from Japan, with descriptions of two new species and host information. Journal of Hymenoptera Research 80: 99-135. https://doi.org/10.3897/jhr.80.56178
Figure 8 Mesosoma of Japanese Gryon spp. AG. japonicum, anterior view B posterior view CG. philippinense, anterior view D posterior view EG. pennsylvanicum, anterior view F posterior view.
Figures 6-7 from: Ganjisaffar F, Talamas EJ, Bon MC, Perring TM (2020) First report and integrated analysis of two native Trissolcus species utilizing Bagrada hilaris eggs in California. Journal of Hymenoptera Research 80: 49-70. https://doi.org/10.3897/jhr.80.57024
Figures 6-7 Trissolcus cosmopeplae, holotype female (USNMENT00989096) 6 head and mesosoma, lateral view 7 head and mesosoma, dorsal view. Scale bars in millimeters.
Figure 7 from: Komeda Y, Mita T, Hirose Y, Yamagishi K (2020) Taxonomic revision of charon-, floridanum- and muscaeforme-groups of Gryon Haliday, 1833 (Hymenoptera, Scelionidae) from Japan, with descriptions of two new species and host information. Journal of Hymenoptera Research 80: 99-135. https://doi.org/10.3897/jhr.80.56178
Figure 7 Mesosoma of Japanese Gryon spp. AG. japonicum, dorsal view B lateral view CG. philippinense, dorsal view D lateral view EG. pennsylvanicum, dorsal view F lateral view.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.