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, second phalanx of the third metacarpal length (2 ph 3 mt), first phalanx of the fourth metacarpal length (1 ph 4 mt) and second phalanx of the fourth metacarpal length (1 ph 4 mt); n indicates the number of individuals collected in Recent surveys of bats from the Andaman Islands, India: diversity, distribution, and echolocation characteristics
, second phalanx of the third metacarpal length (2 ph 3 mt), first phalanx of the fourth metacarpal length (1 ph 4 mt) and second phalanx of the fourth metacarpal length (1 ph 4 mt); n indicates the number of individuals collected
FIG. 1 in A recent inventory of the bats of Mozambique with documentation of seven new species for the country
FIG. 1. Map of Mozambique showing the sites at which bats were captured during this study (2005–2009). The sampling sites are overlaid on a digital elevation model (altitude in metres). The boundaries of the three biogeographic zones (following Parker, 1999) are represented by the two black lines. The southern line follows the Save River, whereas the northern line follows the Zambezi River. The numbers refer to sites and correspond to the site numbers presented in Appendix I
FIG. 4 in Recent surveys of bats (Mammalia: Chiroptera) from China. I. Rhinolophidae and Hipposideridae
FIG. 4. Representative echolocation calls of bats in the family Hipposideridae captured from China during our surveys. See text for data on intraspecific variation. Calls are from time expanded sequences of handheld bats with FFT size 1024 Hz, Hanning window. The species are arranged according to body size from large species (left) to small (right)
FIG. 2 in A recent inventory of the bats of Mozambique with documentation of seven new species for the country
FIG. 2. Map showing the modelled distribution of species richness across Mozambique (only those bat records used in developing the distribution models are presented here, and include some of the localities in Fig. 1, as well as some earlier museum specimens)
FIG. 1 in Recent surveys of bats (Mammalia: Chiroptera) from China. I. Rhinolophidae and Hipposideridae
FIG. 1. Map of China showing the collecting sites during our fieldwork, from 1999 to 2007. Pink is not part of the Peoples' Republic of China. Light green are areas of China that were not surveyed for bats. All provinces that were included in the survey are showed in dark green, including 1-Hainan, 2-Guangdong, 3-Guangxi, 4-Yunnan, 5-Fujian, 6-Jiangxi, 7-Hunan, 8-Guizhou, 9-Sichuan,
FIGURE 1 in Molecular data support monophyly of the recently erected Riggenbachiella (Cestoda: Proteocephalidae), parasites of Neotropical catfishes
FIGURE 1. Phylogram based on maximum likelihood (ML) analysis of partial (D1–D3 domains) of lsrDNA data for species of Riggenbachiella and other selected members of the Proteocephalidae. Taxon names are followed by their voucher accession number, host species, and GenBank accession numbers. Clades C and K (three representatives as outgroup) of de Chambrier et al. (2015) are shown at early nodes. Newly generated sequences are in bold.
Figures 77–81 in Scorpions of the Horn of Africa (Arachnida: Scorpiones). Part XXV. Description of Pandinurus awalei sp. n. and the male of Pandiborellius somalilandus (Kovařík, 2012), with remarks on recent synonymies (Scorpionidae: Pandininae)
Figures 77–81: Pedipalp chela dorsal views. Figures 77–78. Pandipalpus lowei, male (77) and female (78) paratypes from type locality. Figures 79–81. Pandipalpus viatoris, male (79) and female (80) from Democratic Republic of Congo, Kamonga (FKCP), and male (81) from Tanzania, Iringa Province (FKCP).
Figures 3–4 in Scorpions of the Horn of Africa (Arachnida: Scorpiones). Part XXV. Description of Pandinurus awalei sp. n. and the male of Pandiborellius somalilandus (Kovařík, 2012), with remarks on recent synonymies (Scorpionidae: Pandininae)
Figures 3–4. Pandiborellius somalilandus, male from locality No. 19SL in dorsal (3) and ventral (4) views.
Figures 75–76 in Scorpions of the Horn of Africa (Arachnida: Scorpiones). Part XXV. Description of Pandinurus awalei sp. n. and the male of Pandiborellius somalilandus (Kovařík, 2012), with remarks on recent synonymies (Scorpionidae: Pandininae)
Figures 75–76. Pandinurus awalei sp. n., male paratype shortly after maturity ecdysis (75) and young female paratype two months after maturity ecdysis (76).
Figures 67–69 in Scorpions of the Horn of Africa (Arachnida: Scorpiones). Part XXV. Description of Pandinurus awalei sp. n. and the male of Pandiborellius somalilandus (Kovařík, 2012), with remarks on recent synonymies (Scorpionidae: Pandininae)
Figures 67–69. Pandinurus awalei sp. n., left whole hemispermatophore, anterior (67), posterior-concave (68) and convex (69) views. Scale bar: 4 mm.
Figures 12–24 in Scorpions of the Horn of Africa (Arachnida: Scorpiones). Part XXV. Description of Pandinurus awalei sp. n. and the male of Pandiborellius somalilandus (Kovařík, 2012), with remarks on recent synonymies (Scorpionidae: Pandininae)
Figures 12–24: Pedipalp segments. Figures 12–22. Pandiborellius somalilandus, male from locality No. 19SL, pedipalp chela dorsal (12), external (13) and ventral (14) views, patella dorsal (15), external (16) and ventral (17) views, femur and trochanter dorsal (18), and ventral (19) views, movable finger dentition under white (20) and UV (21) light and fixed finger (22) dentition under UV light. Trichobothrial pattern indicated in Figures 12–18. Figures 23–24. Pandinurus awalei sp. n., male holotype, movable finger (23) and fixed finger (24) dentition under UV light.
Figures 54–66 in Scorpions of the Horn of Africa (Arachnida: Scorpiones). Part XXV. Description of Pandinurus awalei sp. n. and the male of Pandiborellius somalilandus (Kovařík, 2012), with remarks on recent synonymies (Scorpionidae: Pandininae)
Figures 54–66: Pandinurus awalei sp. n. Figures 54–61, 64–66. Female paratype, pedipalp chela dorsal (54), external (55) and ventral (56) views, patella dorsal (57), external (58) and ventral (59) views, femur and trochanter dorsal (60), and ventral (61) views, movable finger dentition under white light (64); right chelicera dorsal (65) and ventral (66) aspects. Trichobothrial pattern indicated in Figures 54–59. Figures 62–63. Male holotype, movable finger dentition under UV (62) and white (63) light.
FIGURE 6 in Recent findings of Isthmohyla pictipes (Anura: Hylidae) in Costa Rica: variation and implications for conservation
FIGURE 6. Fluorescence emission in Isthmohyla pictipes under ultraviolet-blue light exposure (365 nm) in the laboratory. (A–B): Female (UCR23364) shown under visible light and UV-Blue flashlight. (C): Female (UCR23365) showing bright yellow fluorescence of the spots that extend from below the forelimb to the base of the toes. (D): Fluorescent bones and tendons seen by transparency in sparsely pigmented areas of limbs and pelvic region of female (UCR23366).
FIGURE 4 in Recent findings of Isthmohyla pictipes (Anura: Hylidae) in Costa Rica: variation and implications for conservation
FIGURE 4. Isthmohyla pictipes from Cuericí. Note the highly variable coloration among all individuals. (A): UCR23366, adult female with a green uniform dorsum, SVL 49.9 mm. Note the bronze colored canthal stripe. (B–C): UCR23364, dorsum and venter of adult female, SVL 52.2 mm. Note the white crenulated dermal flap on the heel. (D): UCR23365, adult female, SVL 54.1 mm. (E–F): UCR23363, dorsum and venter of adult male, SVL 38.8 mm. Color variation during day and night with corresponding ventral photos of an uncollected adult male (G–I) and female (J–L). (G, J): nighttime. (H, K): daytime. (I, L): ventral views.
FIGURE 1 in Recent findings of Isthmohyla pictipes (Anura: Hylidae) in Costa Rica: variation and implications for conservation
FIGURE 1. Distribution map of Isthmohyla pictipes in Costa Rica showing new records from Cuericí and San Gerardo de Dota, the type locality, and museum records from historical localities in the Cordillera Central and the Cordillera de Talamanca.
FIGURES 10–15. 10 in Dimorphopterus blissoides (Hemiptera: Heteroptera: Blissidae): recent spreading of a neonative species in the Pannonian Basin
FIGURES 10–15. 10—habitat of Dimorphopterus blissoides (Baerensprung, 1859) at Tachty, Slovakia. 11–15—galls of Lipara lucens Meigen, 1830 on Phragmites australis with living specimens of Dimorphopterus blissoides (Baerensprung, 1859) (12–15). Slovakia: Tachty, 28.viii.2022. Photos: J. Cunev (10), V. Hemala (11–15).
Distribution. Endemic to Chile, with a disjunct distribution in the forests of Chiloé Island, and on the mainland coastal mountains in Nahuelbuta National Park. Evidence of a new population was foud recently at Punta Chan Chan, N of Valdivia. in Canidae
Distribution. Endemic to Chile, with a disjunct distribution in the forests of Chiloé Island, and on the mainland coastal mountains in Nahuelbuta National Park. Evidence of a new population was foud recently at Punta Chan Chan, N of Valdivia.
Subspecies and Distribution. H.a.aquaticusOgilby,1841—WAfricafromGuineaandSierraLeonetoGhana. H.a.bates:Lydekker,1906—Nigeria,Cameroon,andpresumablyneighboringcountries. H. a. cottoni Lydekker, 1906 — Republic of the Congo, DR Congo, and presumably Uganda. The Water Chevrotain reportedly has a disjunct distribution, occurring in coastal forests from West Africa and in the rainforests of Central Africa from Nigeria to DR Congo, marginally entering Uganda. It has been listed for the following countries in Central Africa: Angola (Cabinda), Cameroon, Central African Republic, DR Congo, Equatorial Guinea, Gabon, Nigeria, Republic of the Congo, and Uganda (Semliki Valley). A record from Angola's Lunda Norte Province, near the Cassai River,is the southernmost record of the species. The species' status in some countries remains unclear. It is apparently absent from the Republic of Benin and Togo (but the speciesis listed as probable in the Ot Basin in Togo); its supposed occurrence in Guinea Bissau and Senegal remains unsupported by evidence. The species was listed for Sierra Leone, although its presence had been called into question. Photographic evidence seems to clarify that the species occurs in Sierra Leone. In 1850, a specimen was recorded from Gambia, but the present status of the species is unclear. Local people report the species from the Boké Préfecture in NW Guinea, which might be the northernmost area from which the species has been recently reported. Extensive field and market surveys there and in the southern Guinea savanna belt did notfind evidence for the species' presence. in Tragulidae
Subspecies and Distribution. H.a.aquaticusOgilby,1841—WAfricafromGuineaandSierraLeonetoGhana. H.a.bates:Lydekker,1906—Nigeria,Cameroon,andpresumablyneighboringcountries. H. a. cottoni Lydekker, 1906 — Republic of the Congo, DR Congo, and presumably Uganda. The Water Chevrotain reportedly has a disjunct distribution, occurring in coastal forests from West Africa and in the rainforests of Central Africa from Nigeria to DR Congo, marginally entering Uganda. It has been listed for the following countries in Central Africa: Angola (Cabinda), Cameroon, Central African Republic, DR Congo, Equatorial Guinea, Gabon, Nigeria, Republic of the Congo, and Uganda (Semliki Valley). A record from Angola's Lunda Norte Province, near the Cassai River,is the southernmost record of the species. The species' status in some countries remains unclear. It is apparently absent from the Republic of Benin and Togo (but the speciesis listed as probable in the Ot Basin in Togo); its supposed occurrence in Guinea Bissau and Senegal remains unsupported by evidence. The species was listed for Sierra Leone, although its presence had been called into question. Photographic evidence seems to clarify that the species occurs in Sierra Leone. In 1850, a specimen was recorded from Gambia, but the present status of the species is unclear. Local people report the species from the Boké Préfecture in NW Guinea, which might be the northernmost area from which the species has been recently reported. Extensive field and market surveys there and in the southern Guinea savanna belt did notfind evidence for the species' presence.
Subspecies and Distribution. A. g. guariba Humboldt, 1812 — Brazilian Atlantic Forest from the Rio Sao Francisco (although the Rio Paraguacu is the northernmost known locality) to the Rio Doce; however, based on his studies of morphology and pelage color patterns Gregorin in 2006 indicated that it extends from the Rio Paraguacu in Bahia State, S along the coast across the lower Rio Jequitinhonha extending inland somewhat into Minas Gerais State, S through the Rio Doce valley as far the Rio Paraiba do Sul Basin in Rio de Janeiro. A. g. clamitans Cabrera, 1940 — Brazilian Atlantic Forest S of Rio Doce (but Gregorin has recently identified howlers of the upper Rio Doce, Rio Matip6 and Caratinga, and the middle and upper Rio Jequitinhonha as marking the N limits of this subspecies) through the S of Espirito Santo to Rio de Janeiro, Sao Paulo, Parana, Santa Catarina, and Rio Grande do Sulstates (S limit is Rio Camaqua Basin in Rio Grande do Sul, 31° 10" S, where the Atlantic Forest gives way to the Pampas grasslands), and inland in the forested E of Minas Gerais ("Zona da Mata") and the Brazilian Highlands; also in NE Argentina (E of the Mts in Misiones Province to ¢.28° S). in Atelidae
Subspecies and Distribution. A. g. guariba Humboldt, 1812 — Brazilian Atlantic Forest from the Rio Sao Francisco (although the Rio Paraguacu is the northernmost known locality) to the Rio Doce; however, based on his studies of morphology and pelage color patterns Gregorin in 2006 indicated that it extends from the Rio Paraguacu in Bahia State, S along the coast across the lower Rio Jequitinhonha extending inland somewhat into Minas Gerais State, S through the Rio Doce valley as far the Rio Paraiba do Sul Basin in Rio de Janeiro. A. g. clamitans Cabrera, 1940 — Brazilian Atlantic Forest S of Rio Doce (but Gregorin has recently identified howlers of the upper Rio Doce, Rio Matip6 and Caratinga, and the middle and upper Rio Jequitinhonha as marking the N limits of this subspecies) through the S of Espirito Santo to Rio de Janeiro, Sao Paulo, Parana, Santa Catarina, and Rio Grande do Sulstates (S limit is Rio Camaqua Basin in Rio Grande do Sul, 31° 10" S, where the Atlantic Forest gives way to the Pampas grasslands), and inland in the forested E of Minas Gerais ("Zona da Mata") and the Brazilian Highlands; also in NE Argentina (E of the Mts in Misiones Province to ¢.28° S).
FIGURE. Habit and habitat of C. spongifolia. A. Single plant ca. 1 m tall, on road bank, at 962 m elevation. B. Scatter of adult plants (arrow heads) in upper area of a recent slip face, above road, at 676 m. C. Plants collected from roadside at 854 m; blades pale, milky-green on underside. D. Same site as B, with young seedling emerging from a bed of moss and liverwort. Photos: PJM. in Colocasia spongifolia sp. nov. (Araceae) in southern China and central Vietnam
FIGURE. Habit and habitat of C. spongifolia. A. Single plant ca. 1 m tall, on road bank, at 962 m elevation. B. Scatter of adult plants (arrow heads) in upper area of a recent slip face, above road, at 676 m. C. Plants collected from roadside at 854 m; blades pale, milky-green on underside. D. Same site as B, with young seedling emerging from a bed of moss and liverwort. Photos: PJM.
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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.