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Figure 10 in Species boundaries and phylogeographic patterns in new species of Nannoniscus (Janiroidea: Nannoniscidae) from the equatorial Pacific nodule province inferred from mtDNA and morphology
Figure 10. Nannoniscus hilario, holotype female (ZMH K-55342, Na23). Confocal laser scanning microscopy images: (A) habitus, dorsal view; (B) habitus, lateral view; (C) habitus, ventral view; (D) mouthparts, ventral view; (E) cephalothorax, lateral view; (F) Plt, ventral view. Scale bars: A–C = 200 µm; D–F = 100 µm.
Figure 17 in Species boundaries and phylogeographic patterns in new species of Nannoniscus (Janiroidea: Nannoniscidae) from the equatorial Pacific nodule province inferred from mtDNA and morphology
Figure 17. Nannoniscus menoti, paratype male (ZMH K-55350, MA14_Iso272): (A) habitus, dorsal view; (B–E) PlpI–IV. Scale bars: A = 250 µm; B–E = 100 µm.
Figure 8 in Species boundaries and phylogeographic patterns in new species of Nannoniscus (Janiroidea: Nannoniscidae) from the equatorial Pacific nodule province inferred from mtDNA and morphology
Figure 8. Nannoniscus hilario, (A, E, I) holotype female (ZMH K-55342, Na23); (B–D, F–H, J–K) paratype female (ZMH K-55341, NB12_Iso020): (A) habitus, dorsal view; (B) AI, peduncular articles 1–4 AII; (C) lMd; (D) rMd; (E) habitus, lateral view; (F) Mxp; (G) Op, ventral view; (H) PlpIII; (I) Plt, ventral view; (J) Urp; (K) Op, lateral view. Scale bars: A, E, I = 200 µm; B–D, F–H, J–K = 100 µm.
Figure 12 in Species boundaries and phylogeographic patterns in new species of Nannoniscus (Janiroidea: Nannoniscidae) from the equatorial Pacific nodule province inferred from mtDNA and morphology
Figure 12. Nannoniscus magdae, (A–B) holotype female (ZMH K-55375, Na26); (C–E, I) paratype female (ZMH K-55373, NB12_Iso099); (F–H) paratype female (ZMH K-55374, Na12): (A) habitus, dorsal view; (B) habitus, lateral view; (C–I) PI-PVII. Scale bars: A–B = 200 µm; C–I = 100 µm.
Figure 13 in Species boundaries and phylogeographic patterns in new species of Nannoniscus (Janiroidea: Nannoniscidae) from the equatorial Pacific nodule province inferred from mtDNA and morphology
Figure 13. Nannoniscus magdae, paratype male (ZMH K-55377, Na49): (A) habitus, dorsal view; (B) PlpI; (C) PlpII. Scale bars: A = 200 µm; B–C = 100 µm.
Figure 16 in Species boundaries and phylogeographic patterns in new species of Nannoniscus (Janiroidea: Nannoniscidae) from the equatorial Pacific nodule province inferred from mtDNA and morphology
Figure 16. Nannoniscus menoti, (A) holotype female (ZMH K-55354, Na27), (B–E, G) paratype female (ZMH K-55356, Na18), (F, H) paratype female (ZMH K-55352, Na6): (A) habitus, dorsal view; (B–H) PI-VII. Scale bars: A = 200 µm; B–H = 100 µm.
High prevalence of SARS-CoV-2 antibodies in pregnant women in the inner city of Johannesburg, Gauteng Province, South Africa
<p>Results of population-based age stratified seroepidemiological investigation in South Africa.</p>
Figure 2 in Ruminants reveal Eocene Asiatic palaeobiogeographical provinces as the origin of diachronous mammalian Oligocene dispersals into Europe
Figure 2. Paleobiogeography of the Eurasiatic ruminants during the Eocene at the genus level. Te localities are from the synthesis of data2,17,18,22,49. Te palinspastic map is modified from Scotese52.
Figure 1 in Ruminants reveal Eocene Asiatic palaeobiogeographical provinces as the origin of diachronous mammalian Oligocene dispersals into Europe
Figure 1. Dentition of Krabimeryx gracilis nov. comb. (Miao, 1982)20 (A, B, G, H), Chiyoumeryx nov. gen. shinaoensis (Miao, 1982)20 (C, D), Chiyoumeryx nov. gen. flavimperatoris nov. sp. (E) and Iberomeryx miaoi nov. sp. (F–I). Krabimeryx gracilis nov. comb. (Miao, 1982)20: (A) IVPP V 6546-1 (holotype), partial skull with right and lef M1–M3; (B) IVPP V 6546-2 (holotype), right fragmented mandible with m2–m3. Chiyoumeryx nov. gen. shinaoensis (Miao, 1982)20: (C) IVPP V 6531 (holotype), right mandible with p2–m3 and tooth socket of p1; (D) IVPP V 6532 (paratype), right fragmented maxillary with P4-M3. Chiyoumeryx nov. gen. flavimperatoris nov. sp.: (E) IVPP V 6547 (holotype), right mandible with p4–m3; Iberomeryx miaoi nov. sp.: (F) IVPP V 6551 (holotype), lef mandible with m1–m3 (mirrored); (G) lower molar Lophiomerycidae dental nomenclature (based on the m3 of IVPP 6546-2): 1 internal postmetacristid, 2 metaconid, 3 external postmetacristid, 4 internal preentocristid, 5 entoconidian groove, 6 external preentocristid, 7 entoconid, 8 posthypoconulidcristid, 9 hypoconulid, 10 prehypoconuldicristid, 11 posthypocristid, 12 hypoconid, 13 prehypocristid, 14 ectostylid, 15 postprotocristid, 16 protoconid, 17 preprotocristid, 18 anterior cingulid; (H) upper molar Lophiomerycidae dental nomenclature (based on the M2 of IVPP 6546-1): 1 postmetacrista, 2 metacone, 3 premetacrista, 4 mesostyle, 5 postparacrista, 6 paracone, 7 paraconid labial groove, 8 preparacrista, 9 parastyle, 10 preprotocrista, 11 anterolingual cingulum, 12 protocone, 13 postprotocrista, 14 entostyle, 15 additional cone, 16 premetaconulecrista, 17 metaconule, 18 postmetaconulecrista; (I) lower molar Tragulidae dental nomenclature (based on the m2 of IVPP V 6551, reversed): 1 metaconid, 2 external postmetacristid, 3 Dorcatherium fold, 4 internal postmetacristid, 5 preentocristid, 6 entoconid, 7 postentocristid, 8 posterior cingulid, 9 posthypocristid, 10 hypoconid, 11 prehypocristid, 12 ectostylid, 13 external postprotocristid, 14 Tragulus fold, 15 internal postprotocristid, 16 protoconid, 17 preprotocristid, 18 paraconid, 19 preparacristid. (J) phylogenetic position and stratigraphie of the Shinao/ Yangjiachong/Xiaerhete ruminants (topology2). a stem Ruminantia, b Archaeomeryx, c Chiyoumeryx nov. gen. and Krabimeryx gracilis, d crown Ruminantia, e Iberomeryx miaoi nov. sp.; 1 lingual view, 2 occlusal view. Scale bare is 1 cm.
Subspecies and Distribution. P. g. gymnocercus Fischer, 1814 — subtropical grasslands of NE Argentina, SE Brazil, Paraguay, and Uruguay. Pg. antiquus Ameghino, 1889 — Pampas grasslands, monte scrublands, and open woodlands of C Argentina. P. g. lordi Massoia, 1982 — Chaco-montane tropical forest ecotone in NW Argentina (Salta & Jujuy Provinces). The subspecific status of the Pampas Fox from Entre Rios Province in Argentina remains unclear, and there are no data regarding the taxonomic position of Bolivian foxes. in Canidae
Subspecies and Distribution. P. g. gymnocercus Fischer, 1814 — subtropical grasslands of NE Argentina, SE Brazil, Paraguay, and Uruguay. Pg. antiquus Ameghino, 1889 — Pampas grasslands, monte scrublands, and open woodlands of C Argentina. P. g. lordi Massoia, 1982 — Chaco-montane tropical forest ecotone in NW Argentina (Salta & Jujuy Provinces). The subspecific status of the Pampas Fox from Entre Rios Province in Argentina remains unclear, and there are no data regarding the taxonomic position of Bolivian foxes.
Distribution. Widespread in the C and W regions of S Africa, reaching to about 15° N in SW Angola. Occupies mainly arid and semi-arid areas, but also occurs in regions with higher precipitation and denser vegetation, such as the fynbos biome of South Africa's Western Cape Province. Cape Foxes have expanded their range over recent decades to the SW, where the species reaches the Atlantic and Indian Ocean coastlines. May occur in SW Swaziland, and possibly also in Lesotho. in Canidae
Distribution. Widespread in the C and W regions of S Africa, reaching to about 15° N in SW Angola. Occupies mainly arid and semi-arid areas, but also occurs in regions with higher precipitation and denser vegetation, such as the fynbos biome of South Africa's Western Cape Province. Cape Foxes have expanded their range over recent decades to the SW, where the species reaches the Atlantic and Indian Ocean coastlines. May occur in SW Swaziland, and possibly also in Lesotho.
Distribution. Widespread in the Tibetan Plateau from Ladakh in India, E across China including parts of the Xinjiang, Gansu, Qinghai, and Sichuan provinces and all of the Xizang. In Nepal, N of the Himalaya, especially in the Mustang area. in Canidae
Distribution. Widespread in the Tibetan Plateau from Ladakh in India, E across China including parts of the Xinjiang, Gansu, Qinghai, and Sichuan provinces and all of the Xizang. In Nepal, N of the Himalaya, especially in the Mustang area.
Subspecies and Distribution. H. p. parvula Sundevall, 1847 — NE South Africa, Mozambique, and Zimbabwe. H. p. wore Thomas, 1919 — NE Mozambique and Tanzania. H. p. mimetra Thomas, 1926 — NW Botswana and N Namibia. H. p. nero Thomas, 1928 — C Namibia. H. p. ruficeps Kershaw, 1922 — Zambia (Southern Province & Kafue area). H. p. undulata Peters, 1852 — N & E Africa from Ethiopia and Sudan to Malawi. H. p. varia Thomas, 1902 — C Africa from Angola to Uganda. in Herpestidae
Subspecies and Distribution. H. p. parvula Sundevall, 1847 — NE South Africa, Mozambique, and Zimbabwe. H. p. wore Thomas, 1919 — NE Mozambique and Tanzania. H. p. mimetra Thomas, 1926 — NW Botswana and N Namibia. H. p. nero Thomas, 1928 — C Namibia. H. p. ruficeps Kershaw, 1922 — Zambia (Southern Province & Kafue area). H. p. undulata Peters, 1852 — N & E Africa from Ethiopia and Sudan to Malawi. H. p. varia Thomas, 1902 — C Africa from Angola to Uganda.
Subspecies and Distribution. P. s. selousi de Winton, 1896 — W Mozambique, NE South Africa (Limpopo & Mpumalanga Provinces), and Zimbabwe. P. s. bechuanae Roberts, 1932 — E Botswana. P. s. ngamiensis Roberts, 1932 — Angola, Zambia, Malawi, N Namibia, and N Botswana. P.s. sengaani Roberts, 1931 — S Mozambique and South Africa (NE KwaZulu-Natal). in Herpestidae
Subspecies and Distribution. P. s. selousi de Winton, 1896 — W Mozambique, NE South Africa (Limpopo & Mpumalanga Provinces), and Zimbabwe. P. s. bechuanae Roberts, 1932 — E Botswana. P. s. ngamiensis Roberts, 1932 — Angola, Zambia, Malawi, N Namibia, and N Botswana. P.s. sengaani Roberts, 1931 — S Mozambique and South Africa (NE KwaZulu-Natal).
Subspecies and Distribution. C. h. humboldtii Gray, 1837 — Patagonia (Chile and Argentina) to the Strait of Magellan. C. h. castaneus d'Orbigny & Gervais, 1847 — C Argentina (S provinces of Buenos Aires & La Pampa to N Rio Negro; it also follows along the Colorado and Black Rivers to Neuquen and S Mendoza). C. h. proteus Thomas, 1902 — subandean C Argentina (Catamarca, La Rioja, San Juan, San Luis & N Mendoza). in Mephitidae
Subspecies and Distribution. C. h. humboldtii Gray, 1837 — Patagonia (Chile and Argentina) to the Strait of Magellan. C. h. castaneus d'Orbigny & Gervais, 1847 — C Argentina (S provinces of Buenos Aires & La Pampa to N Rio Negro; it also follows along the Colorado and Black Rivers to Neuquen and S Mendoza). C. h. proteus Thomas, 1902 — subandean C Argentina (Catamarca, La Rioja, San Juan, San Luis & N Mendoza).
FIGURE 1 in Dichoropetalum viarium (Apiaceae), a new species from Lorestan Province, Western Iran
FIGURE 1. Bayesian analysis phylogenetic tree of nrITS nucleotide sequences. Posterior probability values and bootstrap values of maximum likelihood analysis are shown.
FIGURE 3. Dichoropetalum viarium holotype sheet 1 in Dichoropetalum viarium (Apiaceae), a new species from Lorestan Province, Western Iran
FIGURE 3. Dichoropetalum viarium holotype sheet 1 (MW0595736). Courtesy of the National Depository Bank of Live Systems, Moscow State University.
FIGURE 4 in Dichoropetalum viarium (Apiaceae), a new species from Lorestan Province, Western Iran
FIGURE 4. Mericarp of Dichoropetalum viarium: a—mericarp in dorsal view; b—mericarp structure: 1—exocarp, 2—mesocarp, 3— endosperm, 4—vascular bundle, 5—vitta, 6—mesocarp parenchyma with lignified pitted walls.
FIGURE 8 in Two new species of Amphinemurinae (Plecoptera; Nemouridae) from Yunnan Province, China
FIGURE 8. Mesonemoura diqinga Rehman, Du & Zhao sp. nov., male terminalia. A: Dorsal view; B: Ventral view; C: Lateral view; D: Paraproct, oblique view.
FIGURE 7 in Two new species of Amphinemurinae (Plecoptera; Nemouridae) from Yunnan Province, China
FIGURE 7. Mesonemoura diqinga Rehman, Du & Zhao sp. nov., male terminalia. A: Lateral view; B: Paraproct and cercus, oblique view.
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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.