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Figure 22 from: Lucia M, Gonzalez V (2017) New species and designation of primary types in Neotropical carpenter bees of the genus Xylocopa Latreille (Hymenoptera, Apidae). Journal of Hymenoptera Research 61: 31-48. https://doi.org/10.3897/jhr.61.20345
Figure 22 Schematic representation of the historical changes in the species concept and nomenclature surrounding X. dimidiata Latreille (see text for details). The yellow and blue columns each represent a species concept.
Figure 2 from: Báthori F, Pfliegler WP, Zimmerman C-U, Tartally A (2017) Online image databases as multi-purpose resources: discovery of a new host ant of Rickia wasmannii Cavara (Ascomycota, Laboulbeniales) by screening AntWeb.org. Journal of Hymenoptera Research 61: 85-94. https://doi.org/10.3897/jhr.61.20255
Figure 2 Photograph of a slide-mounted Rickia wasmannii thallus (deposition number: G00562301) from Myrmica hellenica host, recorded on the AntWeb (specimen: CASENT0907653).
Figures 15–18 from: Müller A, Mauss V, Prosi R (2017) Unique nest architecture in the North African osmiine bee Hoplitis (Hoplitis) mucida (Hymenoptera, Megachilidae). Journal of Hymenoptera Research 60: 99-109. https://doi.org/10.3897/jhr.60.20218
Figures 15–18 - Morphological differences in the female sex between Hoplitis mucida (left) and H. stecki (right) (see Table 2): 15–16 Vertex 17–18 Pilosity of tergal discs.
Figures 1–6 from: Müller A, Mauss V, Prosi R (2017) Unique nest architecture in the North African osmiine bee Hoplitis (Hoplitis) mucida (Hymenoptera, Megachilidae). Journal of Hymenoptera Research 60: 99-109. https://doi.org/10.3897/jhr.60.20218
Figures 1–6 - Nests of Hoplitis mucida (see Table 1): 1–2 Nest 1 near Ait Baha in southern Morocco glued to the flat surface of a middle-sized stone 3 Nest 1 opened shortly after its finalization with cell contents removed 4–5 Nest 2 near Ait Baha in southern Morocco glued to the flat surface of a rock 6 Nest 3 originating from near El Kef in northern Tunisia glued to the flat surface of a small stone and photographed after bee emergence.
Figure 6 from: Brothers DJ, Lelej AS (2017) Phylogeny and higher classification of Mutillidae (Hymenoptera) based on morphological reanalyses. Journal of Hymenoptera Research 60: 1-97. https://doi.org/10.3897/jhr.60.20091
Figure 6 - Most-parsimonious tree (see Fig. 5) with branches not supported by resampling (i.e., without positive GC values) collapsed. Terminals in bold are those whose placements differ by more than mere taxonomic level in the classifications of DB and LN (see Appendix 1).
Figure 3 from: Pezzini C, Jahnke SM, Köhler A (2017) Morphological characterization of immature stages of Habrobracon hebetor (Hymenoptera, Braconidae) ectoparasitoid of Ephestia kuehniella (Lepidoptera, Pyralidae). Journal of Hymenoptera Research 60: 157-171. https://doi.org/10.3897/jhr.60.20104
Figure 3 - Immature stages of Habrobracon hebetor (side view): A egg after oviposition B embryo in development C first larval instar D second larval instar E third larval instar F fourth larval instar G cocoon in formation. Scale: (A–C) 0.25 mm (D–G) 0.5 mm.
Figure 14 from: Brothers DJ, Lelej AS (2017) Phylogeny and higher classification of Mutillidae (Hymenoptera) based on morphological reanalyses. Journal of Hymenoptera Research 60: 1-97. https://doi.org/10.3897/jhr.60.20091
Figure 14 - Proposed higher classification of Mutillidae as reflected by the rearranged tree (Fig. 13) of length about 1% greater than the previously preferred tree (Fig. 5) (lengths = 2858 vs 2828 for additive characters, 2671 vs 2646 for non-additive characters). (See Appendix 4 for classification including all currently valid genera and subgenera.)
Figure 2 from: Brothers DJ, Lelej AS (2017) Phylogeny and higher classification of Mutillidae (Hymenoptera) based on morphological reanalyses. Journal of Hymenoptera Research 60: 1-97. https://doi.org/10.3897/jhr.60.20091
Figure 2 - Strict consensus of 618 most-parsimonious trees (length = 2633, ci = 0.20, ri = 0.59), of 101 sub/genera of Mutillidae and 4 outgroups, both sexes, 230 characters all non-additive and equally weighted. Group support (GC) values shown for all groups supported by resampling. Terminals in bold are those whose placements differ by more than mere taxonomic level in the classifications of DB and LN (see Appendix 1).
Figure 13 from: Brothers DJ, Lelej AS (2017) Phylogeny and higher classification of Mutillidae (Hymenoptera) based on morphological reanalyses. Journal of Hymenoptera Research 60: 1-97. https://doi.org/10.3897/jhr.60.20091
Figure 13 - Tree based on preferred tree (see Fig. 5) but with branches re-arranged to make the potential recognizable groups (see Fig. 12) monophyletic (length = 2858, ci = 0.19, ri = 0.60). Group support (GC) values shown for all groups supported by resampling; the highest values obtained when resampling all non-additive or mostly additive characters, using equal weights and implied weights (N = 5), are shown. Terminals in bold are those whose placements differ by more than mere taxonomic level in the classifications of DB and LN (see Appendix 1).
Figure 10 from: Brothers DJ, Lelej AS (2017) Phylogeny and higher classification of Mutillidae (Hymenoptera) based on morphological reanalyses. Journal of Hymenoptera Research 60: 1-97. https://doi.org/10.3897/jhr.60.20091
Figure 10 - Single most-parsimonious tree (raw length = 1622, ci = 0.20, ri = 0.63), of 101 sub/genera of Mutillidae and 4 outgroups, males only, 140 characters many additive and all with implied weighting (N = 5, k = 71). Group support (GC) values shown for all groups supported by resampling. Terminals in bold are those whose placements differ by more than mere taxonomic level in the classifications of DB and LN (see Appendix 1).
Figure 3 from: Brothers DJ, Lelej AS (2017) Phylogeny and higher classification of Mutillidae (Hymenoptera) based on morphological reanalyses. Journal of Hymenoptera Research 60: 1-97. https://doi.org/10.3897/jhr.60.20091
Figure 3 - Single most-parsimonious tree (raw length = 2634, ci = 0.20, ri = 0.59), of 101 sub/genera of Mutillidae and 4 outgroups, both sexes, 230 characters all non-additive and with implied weighting (N = 5, k = 60). Group support (GC) values shown for all groups supported by resampling. Terminals in bold are those whose placements differ by more than mere taxonomic level in the classifications of DB and LN (see Appendix 1).
Figure 3 from: Polilov AA (2017) First record of Megaphragma (Hymenoptera, Trichogrammatidae) in Columbia, and third animal species known to have anucleate neurons. Journal of Hymenoptera Research 60: 181-185. https://doi.org/10.3897/jhr.60.19907
Figure 3 - Internal morphology of Megaphragma caribea: A scheme of sections, dorsal view B–F sagittal sections, DAPI and autofluorescence; ag – abdominal ganglion, cer – cerebrum, gg1,2,3 – pro-, meso-, and metathoracic ganglion.
Figure 3 from: Messas YF, Sobczak JF, Vasconcellos-Neto J (2017) An alternative host of Hymenoepimecis japi (Hymenoptera, Ichneumonidae) on a novel family (Araneae, Araneidae), with notes on behavioral manipulations. Journal of Hymenoptera Research 60: 111-118. https://doi.org/10.3897/jhr.60.14817
Figure 3 - Web modification in Mecynogea biggiba induced by the parasitoid wasp Hymenoepimecis japi. A Normal web of M. biggiba B–C Cocoon webs in lateral view, and D close of the center of the cocoon web. Arrows indicate the dome-shaped part of the web (white), hub of the dome (red) and support threads (green).
Figure 2 from: Polilov AA (2017) First record of Megaphragma (Hymenoptera, Trichogrammatidae) in Columbia, and third animal species known to have anucleate neurons. Journal of Hymenoptera Research 60: 181-185. https://doi.org/10.3897/jhr.60.19907
Figure 2 - Diagnostic characters of Megaphragma caribea, SEM: A head of female B head of male C antennal club, male D antennal club, female E wings F terga of metasoma.
Figure 3 from: Báthori F, Pfliegler WP, Zimmerman C-U, Tartally A (2017) Online image databases as multi-purpose resources: discovery of a new host ant of Rickia wasmannii Cavara (Ascomycota, Laboulbeniales) by screening AntWeb.org. Journal of Hymenoptera Research 61: 85-94. https://doi.org/10.3897/jhr.61.20255
Figure 3 Dorsal (A), head (B) and profile (C) view of the Rickia wasmannii infected Myrmica hellenica worker, recorded on AntWeb (specimen: CASENT0907653), arrows indicate some clearly identifiable R. wasmannii thalli.
Figure 9 from: Trietsch C, Mikó I, Ulmer JM, Deans AR (2017) Translucent cuticle and setiferous patches in Megaspilidae (Hymenoptera, Ceraphronoidea). Journal of Hymenoptera Research 60: 135-156. https://doi.org/10.3897/jhr.60.13692
Figure 9 - A TEM image of the class one gland cells found underneath the synsternal translucent patch in a Dendrocerus sp. (Hymenoptera: Megaspilidae) The arrow points to the secretory duct in the cuticle, while the square outlines the gland cells at the base of these ducts B A closer look at the class one gland cells at the base of one of these ducts. Specimen identifier: IM 5442.
Figure 5 from: Pezzini C, Jahnke SM, Köhler A (2017) Morphological characterization of immature stages of Habrobracon hebetor (Hymenoptera, Braconidae) ectoparasitoid of Ephestia kuehniella (Lepidoptera, Pyralidae). Journal of Hymenoptera Research 60: 157-171. https://doi.org/10.3897/jhr.60.20104
Figure 5 - Scanning electron micrographs of immature stages of Habrobracon hebetor: A detail of the smooth surface of the egg B detail of the setae on the dorsal surface of the thorax and abdomen of third and fourth larval instars and prepupa C detail of the smooth dorsal surface of first and second larval instars with spiracles D detail of a trichoid sensillum E prepupa F female pupa G male pupa.
Figure 8 from: Trietsch C, Mikó I, Ulmer JM, Deans AR (2017) Translucent cuticle and setiferous patches in Megaspilidae (Hymenoptera, Ceraphronoidea). Journal of Hymenoptera Research 60: 135-156. https://doi.org/10.3897/jhr.60.13692
Figure 8 - A A three-dimensional model of a class 3 gland cell found underneath the cuticle. The model shows the cuticle in blue, the gland cell in red, and then secretory duct connecting them in green B A three-dimensional model of a lamellar body.
Figure 5 from: Brothers DJ, Lelej AS (2017) Phylogeny and higher classification of Mutillidae (Hymenoptera) based on morphological reanalyses. Journal of Hymenoptera Research 60: 1-97. https://doi.org/10.3897/jhr.60.20091
Figure 5 - Single most-parsimonious tree (raw length = 2828, ci = 0.19, ri = 0.61), of 101 sub/genera of Mutillidae and 4 outgroups, both sexes, 230 characters many additive and all with implied weighting (N = 5, k = 81). Group support (GC) values shown for all groups supported by resampling. Terminals in bold are those whose placements differ by more than mere taxonomic level in the classifications of DB and LN (see Appendix 1).
Figure 4 from: Brothers DJ, Lelej AS (2017) Phylogeny and higher classification of Mutillidae (Hymenoptera) based on morphological reanalyses. Journal of Hymenoptera Research 60: 1-97. https://doi.org/10.3897/jhr.60.20091
Figure 4 - Strict consensus of 38 most-parsimonious trees (length = 2828, ci = 0.19, ri = 0.61), of 101 sub/genera of Mutillidae and 4 outgroups, both sexes, 230 characters many additive and all equally weighted. Group support (GC) values shown for all groups supported by resampling. Terminals in bold are those whose placements differ by more than mere taxonomic level in the classifications of DB and LN (see Appendix 1).
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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.