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Figure 3 from: Kilpatrick SK, Gibbs J, Mikulas MM, Spichiger S-E, Ostiguy N, Biddinger DJ, Lopez-Uribe MM (2020) An updated checklist of the bees (Hymenoptera, Apoidea, Anthophila) of Pennsylvania, United States of America. Journal of Hymenoptera Research 77: 1-86. https://doi.org/10.3897/jhr.77.49622
Figure 3 Choropleth map of Pennsylvania specifying bee species richness by county. The greater number of species recorded for a county, the darker blue the county is on the map; lighter-colored counties have fewer species reported from them. The number of species reports for counties ranges from one (Cameron Co.) to 246 (Adams Co.).
Figure 4 from: Kilpatrick SK, Gibbs J, Mikulas MM, Spichiger S-E, Ostiguy N, Biddinger DJ, Lopez-Uribe MM (2020) An updated checklist of the bees (Hymenoptera, Apoidea, Anthophila) of Pennsylvania, United States of America. Journal of Hymenoptera Research 77: 1-86. https://doi.org/10.3897/jhr.77.49622
Figure 4 The number of bee species by their most recent years of collection/observation in Pennsylvania. The number within each bar represents the total number of species in the specified time period. Of the species in the state, 366 (83.8%) have been detected between 2000–2018, while at least 56 species (12.8%) have not. No date of collection/observation was available for 15 species (3.4%).
Figure 2 from: Kilpatrick SK, Gibbs J, Mikulas MM, Spichiger S-E, Ostiguy N, Biddinger DJ, Lopez-Uribe MM (2020) An updated checklist of the bees (Hymenoptera, Apoidea, Anthophila) of Pennsylvania, United States of America. Journal of Hymenoptera Research 77: 1-86. https://doi.org/10.3897/jhr.77.49622
Figure 2 Map of northeastern North America with relative bee species richness. The number of bee species reported for Pennsylvania (this study), and neighboring provinces and states, is shown: Connecticut (Zarrillo et al. 2016), Maine (Dibble et al. 2017), Maryland (North American Native Bee Collaborative 2017; Sam Droege, pers. comm.), Michigan (Gibbs et al. 2017a; Jamieson et al. 2019), New York (Danforth and van Dyke 2015; Ascher et al. 2014), Ontario (Sheffield et al. 2017; Bees of Canada 2020), and West Virginia (McKinney 2016).
Figure 1 from: Kilpatrick SK, Gibbs J, Mikulas MM, Spichiger S-E, Ostiguy N, Biddinger DJ, Lopez-Uribe MM (2020) An updated checklist of the bees (Hymenoptera, Apoidea, Anthophila) of Pennsylvania, United States of America. Journal of Hymenoptera Research 77: 1-86. https://doi.org/10.3897/jhr.77.49622
Figure 1 The numbers of bee species by family and per checklist study in Pennsylvania. Blue portions of bars represent the number of species reported in the previous checklist (Donovall and vanEngelsdorp 2010); orange portions of bars denote data from our study. The number inside the blue portion of each bar represents the number of species retained from the previous checklist. Numbers with "-" and enclosed in parentheses indicate taxa removed from the state checklist due either to unverifiable records or synonymy. The numbers with "+", either inside the orange portion or adjacent to the end of each bar, signify new state species records. The families rank from least to greatest number of species as follows: Melittidae (4 spp.), Colletidae (24 spp.), Megachilidae (81 spp.), Andrenidae (100 spp.), Halictidae (110 spp.), and Apidae (118 spp.).
Supplementary material 6 from: Kilpatrick SK, Gibbs J, Mikulas MM, Spichiger S-E, Ostiguy N, Biddinger DJ, Lopez-Uribe MM (2020) An updated checklist of the bees (Hymenoptera, Apoidea, Anthophila) of Pennsylvania, United States of America. Journal of Hymenoptera Research 77: 1-86. https://doi.org/10.3897/jhr.77.49622
López-Uribe Laboratory Database specimen records
Supplementary material 8 from: Kilpatrick SK, Gibbs J, Mikulas MM, Spichiger S-E, Ostiguy N, Biddinger DJ, Lopez-Uribe MM (2020) An updated checklist of the bees (Hymenoptera, Apoidea, Anthophila) of Pennsylvania, United States of America. Journal of Hymenoptera Research 77: 1-86. https://doi.org/10.3897/jhr.77.49622
Mahan et al. (in prep) specimen records
Figures 5-7 from: Waldren GC, Roberts JD, Pitts JP (2020) Phoretic copulation in the velvet ant Sphaeropthalma pensylvanica (Lepeletier) (Hymenoptera, Mutillidae): A novel behavior for Sphaeropthalminae with a synthesis of mating strategies in Mutillidae. Journal of Hymenoptera Research 78: 69-89. https://doi.org/10.3897/jhr.78.55762
Figures 5-7 Examples of each type of mating strategy in Mutillidae5ISC, Dasymutilla foxi (Cockerell, 1894) in Arizona, USA; photograph by Mark H. Brown 6TPC, Myrmosa unicolor Say, 1824 in New York, USA; photograph by A. D. Levine 7MPC, Wallacidia oculata (Fabricius, 1804) in Southern District, Hong Kong; photograph by 'aabbabc.'
Figures 1-4 from: Waldren GC, Roberts JD, Pitts JP (2020) Phoretic copulation in the velvet ant Sphaeropthalma pensylvanica (Lepeletier) (Hymenoptera, Mutillidae): A novel behavior for Sphaeropthalminae with a synthesis of mating strategies in Mutillidae. Journal of Hymenoptera Research 78: 69-89. https://doi.org/10.3897/jhr.78.55762
Figures 1-4 MPC-practicing pair of Sphaeropthalma pensylvanica (Lepeletier, 1845) in Alabama, USA; photographs by Jason D. Roberts.
Figures 2-7 from: Abram PK, McPherson AE, Kula R, Hueppelsheuser T, Thiessen J, Perlman SJ, Curtis CI, Fraser JL, Tam J, Carrillo J, Gates M, Scheffer S, Lewis M, Buffington M (2020) New records of Leptopilina, Ganaspis, and Asobara species associated with Drosophila suzukii in North America, including detections of L. japonica and G. brasiliensis. Journal of Hymenoptera Research 78: 1-17. https://doi.org/10.3897/jhr.78.55026
Figures 2-7 Ganaspis brasiliensis (2, 4); Leptopilina japonica (3, 5); Pachycrepoideus vindemmiae (6); Asobara sp. (7).
Figure 1 from: Abram PK, McPherson AE, Kula R, Hueppelsheuser T, Thiessen J, Perlman SJ, Curtis CI, Fraser JL, Tam J, Carrillo J, Gates M, Scheffer S, Lewis M, Buffington M (2020) New records of Leptopilina, Ganaspis, and Asobara species associated with Drosophila suzukii in North America, including detections of L. japonica and G. brasiliensis. Journal of Hymenoptera Research 78: 1-17. https://doi.org/10.3897/jhr.78.55026
Figure 1 Map of sites where Leptopilina japonica (red circles), or both L. japonica and Ganaspis brasiliensis (green circles) were found in British Columbia, Canada in 2016 and 2019. The red box in the inset shows where the mapped area is situated in North America. Map tiles by Stamen Design, under CC BY 3.0. Data by OpenStreetMap, under ODbL.
Figure 1 from: Geng H, Li C-D, Mottern J, Polaszek A (2020) Synonymy of Idiococcobius Hayat with Coccobius Ratzeburg (Hymenoptera, Aphelinidae): evidenced by a new species from Malaysian Borneo. Journal of Hymenoptera Research 78: 33-40. https://doi.org/10.3897/jhr.78.53064
Figure 1 Coccobius islandicus Geng & Polaszek, sp. nov. A head B antenna C wings. Scale bars: 50 μm.
Figure 1 from: Cruz-Bustos J, Montoya P, Pérez-Lachaud G, Valle-Mora J, Liedo P (2020) Biological attributes of diapausing and non-diapausing Doryctobracon areolatus (Hymenoptera, Braconidae), a parasitoid of Anastrepha spp. (Diptera, Tephritidae) fruit flies. Journal of Hymenoptera Research 78: 41-56. https://doi.org/10.3897/jhr.78.52269
Figure 1 Duration of development of non-diapausing and diapausing Doryctobracon areolatus females and males, parasitizing Anastrepha ludens larvae.
Figure 4 from: Casiraghi A, Espadaler X, Pérez Hidalgo N, Gómez K (2020) Two additions to the Iberian myrmecofauna: Crematogaster inermis Mayr, 1862, a newly established, tree-nesting species, and Trichomyrmex mayri (Forel, 1902), an emerging exotic species temporarily nesting in Spain (Hymenoptera, Formicidae). Journal of Hymenoptera Research 78: 57-68. https://doi.org/10.3897/jhr.78.51858
Figure 4 Crematogaster inermis. Worker head in frontal view, with abraded mandible denticles. (HW 1.125 mm) (Image X. Espadaler).
Figure 1 from: Starr CK, Bhukal R, Ballah ST (2020) Observations of neotropical social wasps (Hymenoptera, Vespidae) preying on eggs and tadpoles of the frog Engystomops pustulosus (Amphibia, Leptodactylidae). Journal of Hymenoptera Research 78: 91-96. https://doi.org/10.3897/jhr.78.54409
Figure 1 Stages in the disintegration of Engystomops pustulosus foam nests. a Stage 1; fresh, domed above the water b Stage 2; distinctly flatter, but still coherent c Stage 3; very flat and losing coherence.
Figure 1 from: Casiraghi A, Espadaler X, Pérez Hidalgo N, Gómez K (2020) Two additions to the Iberian myrmecofauna: Crematogaster inermis Mayr, 1862, a newly established, tree-nesting species, and Trichomyrmex mayri (Forel, 1902), an emerging exotic species temporarily nesting in Spain (Hymenoptera, Formicidae). Journal of Hymenoptera Research 78: 57-68. https://doi.org/10.3897/jhr.78.51858
Figure 1 Robinia pseudoacacia tree (black locust) where Crematogaster inermis were nesting (Valencia, Spain). Black arrow indicates the level of nest entrance (Image X. Espadaler).
Figure 5 from: Cruz-Bustos J, Montoya P, Pérez-Lachaud G, Valle-Mora J, Liedo P (2020) Biological attributes of diapausing and non-diapausing Doryctobracon areolatus (Hymenoptera, Braconidae), a parasitoid of Anastrepha spp. (Diptera, Tephritidae) fruit flies. Journal of Hymenoptera Research 78: 41-56. https://doi.org/10.3897/jhr.78.52269
Figure 5 Net fecundity of Doryctobracon areolatus females from A non-diapausing and B diapausing cohorts.
Figure 2 from: Casiraghi A, Espadaler X, Pérez Hidalgo N, Gómez K (2020) Two additions to the Iberian myrmecofauna: Crematogaster inermis Mayr, 1862, a newly established, tree-nesting species, and Trichomyrmex mayri (Forel, 1902), an emerging exotic species temporarily nesting in Spain (Hymenoptera, Formicidae). Journal of Hymenoptera Research 78: 57-68. https://doi.org/10.3897/jhr.78.51858
Figure 2 Partial view (16 July 2016) of an abandoned date palm grove (Agost, Alicante, Spain) where Crematogaster inermis, Trichomyrmex destructor and T. mayri had been temporary nesting in July 2007 (Image X. Roig).
Figure 3 from: Casiraghi A, Espadaler X, Pérez Hidalgo N, Gómez K (2020) Two additions to the Iberian myrmecofauna: Crematogaster inermis Mayr, 1862, a newly established, tree-nesting species, and Trichomyrmex mayri (Forel, 1902), an emerging exotic species temporarily nesting in Spain (Hymenoptera, Formicidae). Journal of Hymenoptera Research 78: 57-68. https://doi.org/10.3897/jhr.78.51858
Figure 3 Crematogaster inermis, mesosoma lateral view. Bar 0.4 mm. A small specimen (HW 1.050 mm) showing small, but visible, triangular propodeal spines B medium sized specimen (HW 1.150 mm), with merely angulate propodeum C bigger specimen (HW 1.175 mm), with rounded propodeum (Images X. Espadaler).
Figure 3 from: Cruz-Bustos J, Montoya P, Pérez-Lachaud G, Valle-Mora J, Liedo P (2020) Biological attributes of diapausing and non-diapausing Doryctobracon areolatus (Hymenoptera, Braconidae), a parasitoid of Anastrepha spp. (Diptera, Tephritidae) fruit flies. Journal of Hymenoptera Research 78: 41-56. https://doi.org/10.3897/jhr.78.52269
Figure 3 Canonical analysis of adult parasitoids' morphological data from non-diapausing and diapausing Doryctobracon areolatus. A Comparison by type of development B comparison among females C comparison between sexes. The asterisk (*) indicates a significant difference.
Figure 2 from: Cruz-Bustos J, Montoya P, Pérez-Lachaud G, Valle-Mora J, Liedo P (2020) Biological attributes of diapausing and non-diapausing Doryctobracon areolatus (Hymenoptera, Braconidae), a parasitoid of Anastrepha spp. (Diptera, Tephritidae) fruit flies. Journal of Hymenoptera Research 78: 41-56. https://doi.org/10.3897/jhr.78.52269
Figure 2 Canonical analysis of morphological data from puparia containing non-diapausing and diapausing male and female Doryctobracon areolatus parasitoids. The asterisk (*) indicates a significant difference.
ScienceDex guides
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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.