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Figure 4 in Description of two new and six known amphidelphic species of the genus Dorylaimoides Thorne and Swanger, 1936 (Nematoda: Dorylaimida: Tylencholaimoidea) from the Tropical Rainforest, Western Ghats, India
Figure 4. Dorylaimoides parvus Thorne and Swanger, 1936 (LM photographs). (a, b) Anterior region; (c) anterior region showing amphid; (d) pharyngeal region; (e) expanded part of pharynx; (f, g) female genital system; (h) vulval region; (i) female posterior region; (j, k) female posterior end; (l–n) male posterior region showing spicules. Scale bars: a–c, e–h, j–n = 10 μm; d, i = 20 μm.
Figure 2 in Description of two new and six known amphidelphic species of the genus Dorylaimoides Thorne and Swanger, 1936 (Nematoda: Dorylaimida: Tylencholaimoidea) from the Tropical Rainforest, Western Ghats, India
Figure 2. Dorylaimoides teres Thorne and Swanger, 1936 (SEM photographs). (a, b) en face view showing labial papillae and amphid aperture; (c) vulval region; (d) male posterior region (arrows showing ventromedian supplements, adcloacal pair and cloacal aperture); (e) female posterior end, with arrow showing anal opening. Scale bars: a, b = 2 μm; c–e = 10 μm.
Figure 3 in Description of two new and six known amphidelphic species of the genus Dorylaimoides Thorne and Swanger, 1936 (Nematoda: Dorylaimida: Tylencholaimoidea) from the Tropical Rainforest, Western Ghats, India
Figure 3. Dorylaimoides micoletzkyi (de Man, 1921) Thorne and Swanger 1936 (LM photographs unless otherwise specified). (a, b) anterior region; (c) en face view (SEM); (d) anterior region showing amphid; (e) pharyngeal region; (f) expanded part of pharynx; (g) vulval region; (h, i) female genital system; (j) female posterior region; (k) female posterior end; (l) male posterior region (SEM); (m, n) male posterior end. Scale bars: a, b, d, g–i, k–n = 10 μm; c = 2 μm; e, j = 20 μm.
Figure 11 in Description of two new and six known amphidelphic species of the genus Dorylaimoides Thorne and Swanger, 1936 (Nematoda: Dorylaimida: Tylencholaimoidea) from the Tropical Rainforest, Western Ghats, India
Figure 11. Dorylaimoides silvallis sp. nov. (LM photographs). (a, b) Anterior region; (c) anterior region showing amphid; (d) pharyngeal region; (e) expanded part of pharynx; (f, g) female genital system; (h, i) vulval region; (j, k) female posterior end; (l) male posterior region; (m–o) male posterior region showing spicules. Scale bars: a–c, e–i, m–o = 10 μm; d, j–l = 20 μm.
Figure 7. Dorylaimoides mujtabai Baqri, 1991 in Description of two new and six known amphidelphic species of the genus Dorylaimoides Thorne and Swanger, 1936 (Nematoda: Dorylaimida: Tylencholaimoidea) from the Tropical Rainforest, Western Ghats, India
Figure 7. Dorylaimoides mujtabai Baqri, 1991 (LM photographs). (a, b) Anterior region; (c) anterior region showing amphid; (d) pharyngeal region; (e) expanded part of pharynx; (f) vulval region; (g,h) female genital system; (i) female posterior region. (j) male posterior region; (k) male posterior end. Scale bars: a–c, e–k = 10 μm; d = 20 μm.
Figure 1 in Description of two new and six known amphidelphic species of the genus Dorylaimoides Thorne and Swanger, 1936 (Nematoda: Dorylaimida: Tylencholaimoidea) from the Tropical Rainforest, Western Ghats, India
Figure 1. Dorylaimoides teres Thorne and Swanger, 1936 (LM photographs). (a, b) Anterior region; (c) anterior region showing amphid; (d) pharyngeal region; (e) pharyngeal expansion; (f) expanded part of pharynx; (g, h) female genital system; (i) vulval region; (j) female posterior region; (k) female posterior end; (l, m) male posterior end. Scale bars: a–c, e, f, i, k–m = 10 μm; d, g, h, j = 20 μm.
Figure 6 in Description of two new and six known amphidelphic species of the genus Dorylaimoides Thorne and Swanger, 1936 (Nematoda: Dorylaimida: Tylencholaimoidea) from the Tropical Rainforest, Western Ghats, India
Figure 6. Dorylaimoides malabaricus Ahmad and Jairajpuri, 1982 (LM photographs). (a, b) Anterior region; (c) anterior region showing amphid; (d) pharyngeal region; (e, f) expanded part of pharynx; (g) vulval region; (h) female genital system; (i, j) female posterior region; (k) male posterior region; (l, m) male posterior region showing spicules. Scale bars: a–c, e–g, l, m = 10 μm; d, h, j, k = 20 μm; i = 50 µm.
Figure 10 in Description of two new and six known amphidelphic species of the genus Dorylaimoides Thorne and Swanger, 1936 (Nematoda: Dorylaimida: Tylencholaimoidea) from the Tropical Rainforest, Western Ghats, India
Figure 10. Dorylaimoides silvallis sp. nov. (a) Entire female; (b) entire male; (c, d) anterior region; (e) anterior region showing amphid; (f) expanded part of pharynx; (g) pharyngeal region; (h) female genital system; (i) female posterior region; (j, k) male posterior region.
Figure 5. Dorylaimoides leptura Siddiqi, 1965 in Description of two new and six known amphidelphic species of the genus Dorylaimoides Thorne and Swanger, 1936 (Nematoda: Dorylaimida: Tylencholaimoidea) from the Tropical Rainforest, Western Ghats, India
Figure 5. Dorylaimoides leptura Siddiqi, 1965 (LM photographs). (a, b) Anterior region; (c) anterior region showing amphid; (d) pharyngeal region; (e) expanded part of pharynx; (f, g) female genital system; (h) vulval region; (i) female posterior region; (j) male posterior region; (k) male posterior region showing spicules. Scale bars: a–c, e–h, k = 10 μm; d, i, j = 20 μm.
Natural history predicts patterns of thermal vulnerability in amphibians from the Atlantic rainforest of Brazil_supporting information
<p>In the Brazilian Atlantic Rainforest (AF), amphibians (625 species) face habitat degradation leading to stressful thermal conditions that constrain animal activity (e.g. foraging, reproduction). Data on thermal ecology for these species is still scarce. We tested the hypothesis that environmental occupation affects the thermal tolerance of amphibian species more than their phylogenetic relationships. We evaluated patterns of thermal tolerance of 47 amphibian species by assessing critical thermal maxima and warming tolerances, relating these variables with ecological covariates (e.g. adult macro- and microhabitat and site of larval development). We used mean and maximum environmental temperature, ecological covariates, and morphological measurements in the phylogenetic generalized least squares models selection to evaluate which traits better predict thermal tolerance. We did not recover phylogenetic signal under a Brownian model; our results point to a strong association between critical thermal maxima and habitat and development site. Forest species were less tolerant to warm temperatures than open area or generalist species. Species with larvae that develop in lentic environment were more tolerant than those from lotic ones. Thus, species inhabiting forest microclimates are more vulnerable to the synergistic effect of habitat loss and climatic change. We use radar charts as a quick evaluation tool for thermal risk diagnoses using aspects of natural history as axes.</p>
On following pages: 185. Etruscan Shrew (Suncus etruscus); 186. Sri Lankan Shrew (Suncus fellowesgordoni); 187. (Suncus zeylanicus); 190. Asian House Shrew (Suncus murinus); 191. Sri Lankan Highland Shrew (Suncus montanus (Suncus day); 195. Flores Shrew (Suncus mertensi); 196. Black Shrew (Suncus aten); 197. Taita Shrew (Suncus aequatorius Shrew (Suncus infinitesimus); 201. Remy's Pygmy Shrew (Suncus remyi); 202. Lesser Dwarf Shrew (Suncus varilla) Forest Shrew (Sylvisorex johnstonijohnstoni); 206. Akaibe's Forest Shrew (Sylvisorex akaibel); 207. Moon Forest Shrew oriundus); 210. Bioko Forest Shrew (Sylvisorex isabellae); 211. Corbet's Forest Shrew (Sylvisorex corbet)); 212. Bamenda Shrew (Sylvisorex camerunensis); 215. Mount Cameroon Forest Shrew (Sylvisorex morio); 216. Kongana Forest Shrew (Sylvisorex grant); 219. Howell's Forest Shrew (Sylvisorex howell); 220. Armored Hero Shrew (Scutisorex somereni Large-headed Shrew (Paracrocidura schouteden)); 224. Grauer's Large-headed Shrew (Paracrocidura graueri); 225. Piebald Malayan Pygmy Shrew (Suncus malayanus); 188. Bornean Pygmy Shrew (Suncus hose); 189. Jungle Shrew); 192. Nilgiri Highland Shrew (Suncus nigen; 193. Anderson's Shrew (Suncus stoliczkanus); 194. Day's Shrew); 198. Greater Dwarf Shrew (Suncus lixa); 199. Hutu-Tutsi Dwarf Shrew (Suncus hututsi); 200. Least Dwarf; 203. Climbing Shrew (Suncus megalurus); 204. Rwenzori Shrew (Ruwenzorisorex suncoides); 205. Johnston's (Sylvisorex lunaris); 208. Greater Forest Shrew (Sylvisorex ollula); 209. Lesser Forest Shrew (Sylvisorex Forest Shrew (Sylvisorex silvanorum); 213. Rainforest Shrew (Sylvisorex pluvialis); 214. Cameroonian Forest (Sylvisorex konganensis); 217. Volcano Forest Shrew (Sylvisorex vulcanorum); 218. Grant's Forest Shrew); 221. Thor's Hero Shrew (Scutisorex thori); 222. Greater Large-headed Shrew (Paracrocidura maxima); 223. Lesser Shrew (Diplomesodon pulchellus). in Soricidae
On following pages: 185. Etruscan Shrew (Suncus etruscus); 186. Sri Lankan Shrew (Suncus fellowesgordoni); 187. (Suncus zeylanicus); 190. Asian House Shrew (Suncus murinus); 191. Sri Lankan Highland Shrew (Suncus montanus (Suncus day); 195. Flores Shrew (Suncus mertensi); 196. Black Shrew (Suncus aten); 197. Taita Shrew (Suncus aequatorius Shrew (Suncus infinitesimus); 201. Remy's Pygmy Shrew (Suncus remyi); 202. Lesser Dwarf Shrew (Suncus varilla) Forest Shrew (Sylvisorex johnstonijohnstoni); 206. Akaibe's Forest Shrew (Sylvisorex akaibel); 207. Moon Forest Shrew oriundus); 210. Bioko Forest Shrew (Sylvisorex isabellae); 211. Corbet's Forest Shrew (Sylvisorex corbet)); 212. Bamenda Shrew (Sylvisorex camerunensis); 215. Mount Cameroon Forest Shrew (Sylvisorex morio); 216. Kongana Forest Shrew (Sylvisorex grant); 219. Howell's Forest Shrew (Sylvisorex howell); 220. Armored Hero Shrew (Scutisorex somereni Large-headed Shrew (Paracrocidura schouteden)); 224. Grauer's Large-headed Shrew (Paracrocidura graueri); 225. Piebald Malayan Pygmy Shrew (Suncus malayanus); 188. Bornean Pygmy Shrew (Suncus hose); 189. Jungle Shrew); 192. Nilgiri Highland Shrew (Suncus nigen; 193. Anderson's Shrew (Suncus stoliczkanus); 194. Day's Shrew); 198. Greater Dwarf Shrew (Suncus lixa); 199. Hutu-Tutsi Dwarf Shrew (Suncus hututsi); 200. Least Dwarf; 203. Climbing Shrew (Suncus megalurus); 204. Rwenzori Shrew (Ruwenzorisorex suncoides); 205. Johnston's (Sylvisorex lunaris); 208. Greater Forest Shrew (Sylvisorex ollula); 209. Lesser Forest Shrew (Sylvisorex Forest Shrew (Sylvisorex silvanorum); 213. Rainforest Shrew (Sylvisorex pluvialis); 214. Cameroonian Forest (Sylvisorex konganensis); 217. Volcano Forest Shrew (Sylvisorex vulcanorum); 218. Grant's Forest Shrew); 221. Thor's Hero Shrew (Scutisorex thori); 222. Greater Large-headed Shrew (Paracrocidura maxima); 223. Lesser Shrew (Diplomesodon pulchellus).
Distribution. Endemic to Sumatra; it seems widely distributed from upper montane rainforest in W Sumatra to hillsides in E & S Sumatra. in Soricidae
Distribution. Endemic to Sumatra; it seems widely distributed from upper montane rainforest in W Sumatra to hillsides in E & S Sumatra.
Distribution. Lacandona Rainforest, Chiapas (SE Mexico); it might also be found in adjacent Guatemala or throughout the Usumacinta-Lacantin rivers plains. in Soricidae
Distribution. Lacandona Rainforest, Chiapas (SE Mexico); it might also be found in adjacent Guatemala or throughout the Usumacinta-Lacantin rivers plains.
Distribution. Narrowly distributed in C African rainforests of S Cameroon, SW Central African Republic, Equatorial Guinea, Gabon, and NW Republic of the Congo. in Muridae
Distribution. Narrowly distributed in C African rainforests of S Cameroon, SW Central African Republic, Equatorial Guinea, Gabon, and NW Republic of the Congo.
On following pages: 446. Glover Allen's Shaggy Rat (Dasymys alleni); 447. Middle Shaggy Rat (Dasymys medius); 448. Rwandan Shaggy Rat (Dasymys rwandae); 449. Tanzanian Shaggy Rat (Dasymys sua); 450. CrawfordCabral's Shaggy Rat (Dasymys cabrali); 451. Angolan Shaggy Rat (Dasymys nudipes); 452. Roberts's Shaggy Rat (Dasymys robertsii); 453. Cape Shaggy Rat (Dasymys capensis), 454. African Shaggy Rat (Dasymys incomtus); 455. Ethiopian Thicket Rat (Grammomys minnae); 456. Arid Woodland Thicket Rat (Grammomys aridulus); 457. Bunting's Thicket Rat (Grammomys buntingi); 458. Western Rainforest Thicket Rat (Grammomys poensis); 459. Albertine Rift Thicket Rat (Grammomys dryas); 460. Eastern Rainforest Thicket Rat (Grammomys kuru); 461. Short-snouted Thicket Rat (Grammomys brevirostris); 462. Gray-headed Thicket Rat (Grammomys caniceps); 463. Mount Kenya Thicket Rat (Grammomys gigas); 464. East African Thicket Rat (Grammomys ibeanus); 465. Macmillan's Thicket Rat (Grammomys macmillani); 466. Selous's Thicket Rat (Grammomys selousi); 467. in Muridae
On following pages: 446. Glover Allen's Shaggy Rat (Dasymys alleni); 447. Middle Shaggy Rat (Dasymys medius); 448. Rwandan Shaggy Rat (Dasymys rwandae); 449. Tanzanian Shaggy Rat (Dasymys sua); 450. CrawfordCabral's Shaggy Rat (Dasymys cabrali); 451. Angolan Shaggy Rat (Dasymys nudipes); 452. Roberts's Shaggy Rat (Dasymys robertsii); 453. Cape Shaggy Rat (Dasymys capensis), 454. African Shaggy Rat (Dasymys incomtus); 455. Ethiopian Thicket Rat (Grammomys minnae); 456. Arid Woodland Thicket Rat (Grammomys aridulus); 457. Bunting's Thicket Rat (Grammomys buntingi); 458. Western Rainforest Thicket Rat (Grammomys poensis); 459. Albertine Rift Thicket Rat (Grammomys dryas); 460. Eastern Rainforest Thicket Rat (Grammomys kuru); 461. Short-snouted Thicket Rat (Grammomys brevirostris); 462. Gray-headed Thicket Rat (Grammomys caniceps); 463. Mount Kenya Thicket Rat (Grammomys gigas); 464. East African Thicket Rat (Grammomys ibeanus); 465. Macmillan's Thicket Rat (Grammomys macmillani); 466. Selous's Thicket Rat (Grammomys selousi); 467.
FIGURE 5 in New species of Quiva (Paraquiva) Cadena-Castañeda & Gorochov, 2013 (Orthoptera: Tettigoniidae: Phaneropterinae: Dysoniini) from Brazilian Amazon Rainforest
FIGURE 5. Quiva (Paraquiva) obscura sp. nov., stridulatory file of male. A: left file; B: right file.
FIGURE 1 in New species of Quiva (Paraquiva) Cadena-Castañeda & Gorochov, 2013 (Orthoptera: Tettigoniidae: Phaneropterinae: Dysoniini) from Brazilian Amazon Rainforest
FIGURE 1. Pictorial key to the species of Quiva (Paraquiva) Cadena-Castañeda & Gorochov, 2013. Illustrations adapted from Cadena-Castañeda & Gorochov, 2013.
FIGURE 4 in New species of Quiva (Paraquiva) Cadena-Castañeda & Gorochov, 2013 (Orthoptera: Tettigoniidae: Phaneropterinae: Dysoniini) from Brazilian Amazon Rainforest
FIGURE 4. Quiva (Paraquiva) obscura sp. nov., left tegmina of male in dorsal view. Abbreviations: AP: Posterior anal vein; AA: anterior anal vein; CuA: anterior cubital vein; CuP: posterior cubital vein; MA: anterior median vein; MP: posterior median vein; R: radial vein; Sc: subcostal vein.
FIGURE 3 in New species of Quiva (Paraquiva) Cadena-Castañeda & Gorochov, 2013 (Orthoptera: Tettigoniidae: Phaneropterinae: Dysoniini) from Brazilian Amazon Rainforest
FIGURE 3. Quiva (Paraquiva) obscura sp. nov., holotype male. A: habitus, dorsal view; B: head, frontal view; C: head and pronotum, dorsal view; D: head and pronotum, lateral view; E: Thoracic sternites, ventral view; F: foreleg, lateral view; G: midleg, lateral view; H: hindleg, lateral view; I–J: Terminalia in ventral and dorsal view respectively; K: Apex of cerci, dorsal view. Abbreviations: Mes: mesobasisternum; Met: metabasisternum; Cer: cerci; Sty: styli; Pl: subgenital plate.
FIGURE 2 in New species of Quiva (Paraquiva) Cadena-Castañeda & Gorochov, 2013 (Orthoptera: Tettigoniidae: Phaneropterinae: Dysoniini) from Brazilian Amazon Rainforest
FIGURE 2. Quiva (Paraquiva) angieae Cadena-Castañeda, 2013. Holotype male. A: habitus, lateral view; B: habitus, dorsal view; C: holotype labels; D: head, frontal view. Photos: Oscar Cadena-Castañeda.
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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.