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Subspecies and Distribution. L.a.americanusErxleben,1777—C&ECanada(SENorthwestTerritories,SENunavut,mostAlberta,Saskatchewan,andManitoba,S&SEOntario,Quebec,L.a.,andNewfoundland),alsoinNCUSA(NEMontanaandNorthDakota). L.a.bairdiiHayden,1869—SWCanada(SEBritishColumbiaandSWAlberta)andWCUSA(W&CMontana,Idaho,W&SCWyoming,NE&CUtah,NW&CColorado,andNCNewMexico). L.a.cascadensisNelson,1907—SWCanada(SCBritishColumbia)andNWUSA(SC,C&NCWashington). L.a.columbiensisRhoads,1895—RockyMtsinSWCanada(SEBritishColumbia,WCAlberta),andNWUSA(NEtipofWashington). L.a.dalliMerriam,1900—Alaska(USA)andNWCanada(NWAlberta,NBritishColumbia,YukonexcepttheNtip,S&WNorthwestTerritories). L.a.klamathensisMerriam,1899—WUSA(SWOregonandNCalifornia). L.a.oregonusOrr,1934—WUSA(NE&COregon). L.a.pallidusCowan,1938—SWCanada(WC&CBritishColumbia). L.a.phaeonotusJ.A.Allen,1899—WGreatL.a.RegioninSCCanada(SEtipofSaskatchewan,SManitoba,SWOntario)andNCUSA(NEtipofNorthDakota,Minnesota,NWisconsin,andNMichigan). L.a.pineusDalquest,1942—SWCanada(SCtipofBritishColumbia)andNWUSA(EWashington,NIdaho,NWtipofMontana). L.a.seclususBaker&Hankins,1950—NCUSA(SCtipofMontana,NCtipofWyoming). L.a.struthopusBangs,1898—ECanada(EQuebec,NewBrunswick,NovaScotia,PrinceEdwardI)andNEUSA(Maine). L.a.tahoensisOrr,1933—WUSA(ECCaliforniaandWCNevada). L.a.virgtnianusHarlan,1825—SECanada(SOntario,SQuebec)andNE&EUSA(fromMainetoPennsylvaniaandextremeNEOhio,TennesseeandNorthCarolina). L. a. washingtonBaird, 1855 — SW Canada (SW tip of British Columbia) and NW USA (W Washington and W Oregon). The Snowshoe Hare has been introduced by founder individuals of unknown subspecies affiliation to Kodiak I (Alaska) and Anticosti I (Quebec, Canada). in Leporidae
Subspecies and Distribution. L.a.americanusErxleben,1777—C&ECanada(SENorthwestTerritories,SENunavut,mostAlberta,Saskatchewan,andManitoba,S&SEOntario,Quebec,L.a.,andNewfoundland),alsoinNCUSA(NEMontanaandNorthDakota). L.a.bairdiiHayden,1869—SWCanada(SEBritishColumbiaandSWAlberta)andWCUSA(W&CMontana,Idaho,W&SCWyoming,NE&CUtah,NW&CColorado,andNCNewMexico). L.a.cascadensisNelson,1907—SWCanada(SCBritishColumbia)andNWUSA(SC,C&NCWashington). L.a.columbiensisRhoads,1895—RockyMtsinSWCanada(SEBritishColumbia,WCAlberta),andNWUSA(NEtipofWashington). L.a.dalliMerriam,1900—Alaska(USA)andNWCanada(NWAlberta,NBritishColumbia,YukonexcepttheNtip,S&WNorthwestTerritories). L.a.klamathensisMerriam,1899—WUSA(SWOregonandNCalifornia). L.a.oregonusOrr,1934—WUSA(NE&COregon). L.a.pallidusCowan,1938—SWCanada(WC&CBritishColumbia). L.a.phaeonotusJ.A.Allen,1899—WGreatL.a.RegioninSCCanada(SEtipofSaskatchewan,SManitoba,SWOntario)andNCUSA(NEtipofNorthDakota,Minnesota,NWisconsin,andNMichigan). L.a.pineusDalquest,1942—SWCanada(SCtipofBritishColumbia)andNWUSA(EWashington,NIdaho,NWtipofMontana). L.a.seclususBaker&Hankins,1950—NCUSA(SCtipofMontana,NCtipofWyoming). L.a.struthopusBangs,1898—ECanada(EQuebec,NewBrunswick,NovaScotia,PrinceEdwardI)andNEUSA(Maine). L.a.tahoensisOrr,1933—WUSA(ECCaliforniaandWCNevada). L.a.virgtnianusHarlan,1825—SECanada(SOntario,SQuebec)andNE&EUSA(fromMainetoPennsylvaniaandextremeNEOhio,TennesseeandNorthCarolina). L. a. washingtonBaird, 1855 — SW Canada (SW tip of British Columbia) and NW USA (W Washington and W Oregon). The Snowshoe Hare has been introduced by founder individuals of unknown subspecies affiliation to Kodiak I (Alaska) and Anticosti I (Quebec, Canada).
Subspecies and Distribution. L.n.nigricollisF.Cuvier,1823—SIndia(SoftheGodavariRiver). L.n.aryabertensisHodgson,1844—SCNepal. L.n.dayanusBlanford,1874—SEPakistanandNWIndia(GreatIndianDesert). L.n.ruficaudatusE.GeoffroySaint-Hilaire,1826—EPakistan,NIndia,SNepal,Bangladesh,Bhutan,exceptthehigherreachesoftheHimalayasandthemangroveareaswithintheSundarbans. L.n.sadiyaKloss,1918—NEIndia(Assam). L.n.simcoxiWroughton,1912—CIndia(NMaharashtraandMadhyaPradesh). L. n. singhala Wroughton, 1915 — Sri Lanka. Indian hares (probably ruficaudatus) also occur in extreme E Afghanistan, in the border areas with Pakistan. Situation in Java is debated and the so called "Javan Hare" might be native there. The species has been introduced by founder individuals of either unknown subspeciesaffiliation or belonging to various subspecies into Comoro, Mayotte, Madagascar, Réunion (including Gunners Quoin I), Mauritius (Agaléga Is), Seychelles (Cousin I), and Andaman Is in the Indian Ocean, and into New Guinea. In Gunners Quoin the Indian Hare has been eradicated. in Leporidae
Subspecies and Distribution. L.n.nigricollisF.Cuvier,1823—SIndia(SoftheGodavariRiver). L.n.aryabertensisHodgson,1844—SCNepal. L.n.dayanusBlanford,1874—SEPakistanandNWIndia(GreatIndianDesert). L.n.ruficaudatusE.GeoffroySaint-Hilaire,1826—EPakistan,NIndia,SNepal,Bangladesh,Bhutan,exceptthehigherreachesoftheHimalayasandthemangroveareaswithintheSundarbans. L.n.sadiyaKloss,1918—NEIndia(Assam). L.n.simcoxiWroughton,1912—CIndia(NMaharashtraandMadhyaPradesh). L. n. singhala Wroughton, 1915 — Sri Lanka. Indian hares (probably ruficaudatus) also occur in extreme E Afghanistan, in the border areas with Pakistan. Situation in Java is debated and the so called "Javan Hare" might be native there. The species has been introduced by founder individuals of either unknown subspeciesaffiliation or belonging to various subspecies into Comoro, Mayotte, Madagascar, Réunion (including Gunners Quoin I), Mauritius (Agaléga Is), Seychelles (Cousin I), and Andaman Is in the Indian Ocean, and into New Guinea. In Gunners Quoin the Indian Hare has been eradicated.
Tumor-induced Osteomalacia: A Systematic Review and Individual Patient's Data Analysis
<p>Abstract Context Tumor-induced osteomalacia (TIO) is a rare paraneoplastic syndrome, usually caused by small, benign, and slow-growing phosphaturic mesenchymal tumors. Clinically, TIO is characterized by renal phosphate leak, causing hypophosphatemia and osteomalacia. This review was performed to assess the clinical characteristics of TIO patients described worldwide so far. Evidence Acquisition On June 26, 2021, a systematic search was performed in Medline, Google Scholar, Google book, and Cochrane Library using the terms: "tumor induced osteomalacia," "oncogenic osteomalacia," "hypophosphatemia." There were no language restrictions. This review was performed according to Preferred Reporting Items for Systematic reviews and Meta-Analyses criteria. Evidence Results Overall, 1725 TIO cases were collected. TIO was more frequent in adult men, who showed a higher incidence of fractures compared with TIO women. The TIO-causing neoplasms were identified in 1493 patients. The somatostatin receptor-based imaging modalities have the highest sensitivity for the identification of TIO-causing neoplasms. TIO-causing neoplasms were equally located in bone and soft tissues; the latter showed a higher prevalence of fractures and deformities. The surgery is the preferred TIO definitive treatment (successful in &gt; 90% of patients). Promising nonsurgical therapies are treatments with burosumab in TIO patients with elevated fibroblast growth factor-23 levels, and with radiolabeled somatostatin analogs in patients with TIO-causing neoplasm identified by somatostatin receptor-based imaging techniques. Conclusion TIO occurs preferentially in adult men. The TIO clinical expressiveness is more severe in men as well as in patients with TIO-causing neoplasms located in soft tissues. Treatments with burosumab and with radiolabeled somatostatin analogs are the most promising nonsurgical therapies.</p>
Early postnatal individual vocal recognition in a highly colonial mammal species
<p>Dataset associated with the article entitled 'Early postnatal individual vocal recognition in a highly colonial mammal species'</p>
Distribution. Restricted to Réunion I; there is an isolated record from S Ethiopia, some several hundred kilometers from the coast. This record represents a vagrant or introduced individual, and the species does not normally occur in Africa. in Molossidae
Distribution. Restricted to Réunion I; there is an isolated record from S Ethiopia, some several hundred kilometers from the coast. This record represents a vagrant or introduced individual, and the species does not normally occur in Africa.
Data from: Hidden dynamics in the unfolding of individual bacteriorhodopsin proteins
Protein folding occurs as a set of transitions between structural states within an energy landscape. An oversimplified view of the folding process emerges when transiently populated states are undetected because of limited instrumental resolution. Using force spectroscopy optimized for 1-microsecond resolution, we reexamined the unfolding of individual bacteriorhodopsin molecules in native lipid bilayers. The experimental data reveal the unfolding pathway in unprecedented detail. Numerous newly detected intermediates—many separated by as few as two or three amino acids—exhibited complex dynamics, including frequent refolding and state occupancies of <10 μs. Equilibrium measurements between such states enabled the folding free-energy landscape to be deduced. These results sharpen the picture of the mechanical unfolding of membrane proteins and, more broadly, enable experimental access to previously obscured protein dynamics.
FIGURE. Drosera hirtella: a, specimen Saint-Hilaire B1-1762bis (P00749158), with the designated lectotype highlighted; b, detail of the lectotype, showing the ascending scape and leaves with obovate lamina; c, detail of the individual to the left of the lectotype, representing the "western morphotype", with narrowly obovate lamina. Image extracted from A. de Saint-Hilaire virtual herbarium (2020). in A synopsis of the genus Drosera (Droseraceae) in Brazil
FIGURE. Drosera hirtella: a, specimen Saint-Hilaire B1-1762bis (P00749158), with the designated lectotype highlighted; b, detail of the lectotype, showing the ascending scape and leaves with obovate lamina; c, detail of the individual to the left of the lectotype, representing the "western morphotype", with narrowly obovate lamina. Image extracted from A. de Saint-Hilaire virtual herbarium (2020).
FIGURE. Drosera hirtella (a–i): a, b, c, habit of the "type morphotype"; d, habit of the "western morphotype"; e, rosette of the "type morphotype"; f, emerging inflorescence, highlighting the red scape with red eglandular trichomes characteristic of the species; g, fertile individuals of D. hirtella (left plant, with inflorescence emerging to the bottom) and D. lutescens (right plant, with inflorescence emerging to the top left) growing under shaded conditions side by side, highlighting the morphological differences between the two species regarding leaf shape and scape and indumentum color; h, i, flower. a–c, f and h at Serra do Cipó, MG; d and h at Chapada dos Veadeiros, GO; e at Diamantina, MG; g at Cristalina, GO. Photo credits: all by PMG. in A synopsis of the genus Drosera (Droseraceae) in Brazil
FIGURE. Drosera hirtella (a–i): a, b, c, habit of the "type morphotype"; d, habit of the "western morphotype"; e, rosette of the "type morphotype"; f, emerging inflorescence, highlighting the red scape with red eglandular trichomes characteristic of the species; g, fertile individuals of D. hirtella (left plant, with inflorescence emerging to the bottom) and D. lutescens (right plant, with inflorescence emerging to the top left) growing under shaded conditions side by side, highlighting the morphological differences between the two species regarding leaf shape and scape and indumentum color; h, i, flower. a–c, f and h at Serra do Cipó, MG; d and h at Chapada dos Veadeiros, GO; e at Diamantina, MG; g at Cristalina, GO. Photo credits: all by PMG.
Distribution. Raja Ampat Is (Gebe, Gag, Waigeo, and Batanta), Schouten Is (Biak-Supiori and Owi) off NWNew Guinea; it possibly may be found on MisoolI, a single individual reported from Salawati I probably represents a vagrant. in Pteropodidae
Distribution. Raja Ampat Is (Gebe, Gag, Waigeo, and Batanta), Schouten Is (Biak-Supiori and Owi) off NWNew Guinea; it possibly may be found on MisoolI, a single individual reported from Salawati I probably represents a vagrant.
Graph-based Leaf–Wood Separation Method for Individual Trees Using Terrestrial Lidar Point Clouds: Labeled validation data
<p>Set of 10 manually labeled point clouds used in the performance assessment of "Graph-based Leaf–Wood Separation Method for Individual Trees Using Terrestrial Lidar Point Clouds". This dataset is a collection of single trees scanned from different regions covering tropical, temperate, and boreal species—with heights ranging from 5.4 to 43.7 m, using the Riegl VZ-400 and Leica ScanStation C10 terrestrial laser scanner. These data have been preprocessed. For the original data, see https://doi.org/10.5061/dryad.10hq7;<br> https://doi.org/10.5061/dryad.np5hqbzp6;<br> https://doi.org/10.1594/PANGAEA.942856.</p>
Distribution. NE Mali, EC & SE Sudan, SE South Sudan, and NE Ethiopia. There is also a record from ancient Egypt in Thebes where a mummified individual has recently been identified, although status of the species there is uncertain considering no individuals have been observed there in recent times. in Soricidae
Distribution. NE Mali, EC & SE Sudan, SE South Sudan, and NE Ethiopia. There is also a record from ancient Egypt in Thebes where a mummified individual has recently been identified, although status of the species there is uncertain considering no individuals have been observed there in recent times.
FIGURE 42. Live individuals. A in The tribe Dysoniini part VI: Phylogeny, biogeography and evolutionary trends of the lichen katydid genera (Orthoptera: Tettigoniidae: Phaneropterinae). Eleventh contribution to the suprageneric organization of Neotropical phaneropterines
FIGURE 42. Live individuals. A. Dissonulichen (Dissonulichen) simplicipes. B. Lichenomorphus sp. C. Dysonia cf. holgeri. D. L. montealegrezi. E. L. berenzini. F. L. carlosmendezi. G. Dysonia sp. H. Q. sharovi. (Photos: A, B and E. J. Monzón. C. L. Huamán. F. M. Martins. H. A. Anker).
FIGURE 44. Live individuals. A–B. Hammatofera nodicornis. C in The tribe Dysoniini part VI: Phylogeny, biogeography and evolutionary trends of the lichen katydid genera (Orthoptera: Tettigoniidae: Phaneropterinae). Eleventh contribution to the suprageneric organization of Neotropical phaneropterines
FIGURE 44. Live individuals. A–B. Hammatofera nodicornis. C. Dissonulichen (Dissonulichospinus) diffusus. D. Machimoides cf. peru. E. Machima cf. scalprum. F. Yungasacris peruviensis. G. Quiva (Paraquiva) angieae. (Photos: A, B, D. E. Branco. C. J. Chamorro. D. Chan To. F. R. Hoyer. G. accerfoundation).
FIGURE 43. Live individuals. A. Lichenodraculus matti. B. Markia arizae. C. M. major. D. M. hystrix. E. Apolinaria hygracantha. F. Paraphidnia brevicristata G in The tribe Dysoniini part VI: Phylogeny, biogeography and evolutionary trends of the lichen katydid genera (Orthoptera: Tettigoniidae: Phaneropterinae). Eleventh contribution to the suprageneric organization of Neotropical phaneropterines
FIGURE 43. Live individuals. A. Lichenodraculus matti. B. Markia arizae. C. M. major. D. M. hystrix. E. Apolinaria hygracantha. F. Paraphidnia brevicristata G. Anaphidna rubricorpus. (Photos: A. L. Salagaje. B. A. Kay. C. J. Monzón. E. F. Arango. F. A. Anker. G. J. Cardona).
Nesokia is sister to Bandicota and are nested in Rattus phylogenetically, making Rat- tus paraphyletic. Tarsomys, Limnomys, and Diplothrix are also phylogenetically in Rat- tus, and the clade is in need of focused re- vision at the generic level. Nesokia bunnui was originally described as a separate ge-nus, Erythronesokia, because it is morphologically very distinctive from N. indica. Type specimen was destroyed during the Iraq War, and a neotype was recently designated to replace it. Monotypic. Distribution. Tigris and Euphrates river valleys, SE Iraq. Descriptive notes. Head—body 230-260 mm, tail 205-270 mm, ear 18-21 mm, hindfoot 49-58 mm; weight 519 g. The Long-tailed Bandicoot Rat is larger than the Short-tailed Bandicoot Rat (N. indica). Pelage is soft and woolly, interspersed with harsher coarse hair and long black hairs near mid-back. Dorsum is fawn to ocherous red, washed with purple or chestnuton darker individuals. Hairs are basally slate-gray and distally rufous, occasionally with whitish or black tips. Muzzle is drab. Sides arefawn, with gray edge toward venter. Venteris whitish, extending onto cheeks where the same pattern from gray to fawn to dorsal pelage occurs. Feet are large and robust, being light brown and well-furred dorsally. Claws are amber on forefeet and dull brown on hindfeet; pollux is extremely small. Ears are moderately long and brownish, with no hair internally. Tail is ¢.82-104% of head-body length and deep brownish drab, interspersed with visible white hair. Skull is large and robust, similarly to the Short-tailed Bandicoot Rat. Habitat. Marsh and swamp land. Food and Feeding. No information. Breeding. No information. Activity patterns. The Long-tailed Bandicoot Rat is terrestrial, although it isfound in swampy and marshy areas and is probably amphibious. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Endangered on The IUCN Red List. The Longtailed Bandicoot Rat is apparently rare and is known from very few specimens. Marsh and swamp habitats in which it is found were completely destroyed during the Iraq War by draining, war damage, and agricultural expansion. In recent years, flooding from Tigris and Euphrates rivers and high snow fall and melt haveresulted in partial restoration ofits native habitat, although restoration is not a complete. Populations are now probably highly fragmented. Bibliography. Al-Ansari et al. (2012), Al-Robaae & Felten (1990), Khajuria (1981), Krystufek et al. (2017), Musser & Carleton (2005), Richardson & Hussain (2006), Stuart (2008). in Muridae
Nesokia is sister to Bandicota and are nested in Rattus phylogenetically, making Rat- tus paraphyletic. Tarsomys, Limnomys, and Diplothrix are also phylogenetically in Rat- tus, and the clade is in need of focused re- vision at the generic level. Nesokia bunnui was originally described as a separate ge-nus, Erythronesokia, because it is morphologically very distinctive from N. indica. Type specimen was destroyed during the Iraq War, and a neotype was recently designated to replace it. Monotypic. Distribution. Tigris and Euphrates river valleys, SE Iraq. Descriptive notes. Head—body 230-260 mm, tail 205-270 mm, ear 18-21 mm, hindfoot 49-58 mm; weight 519 g. The Long-tailed Bandicoot Rat is larger than the Short-tailed Bandicoot Rat (N. indica). Pelage is soft and woolly, interspersed with harsher coarse hair and long black hairs near mid-back. Dorsum is fawn to ocherous red, washed with purple or chestnuton darker individuals. Hairs are basally slate-gray and distally rufous, occasionally with whitish or black tips. Muzzle is drab. Sides arefawn, with gray edge toward venter. Venteris whitish, extending onto cheeks where the same pattern from gray to fawn to dorsal pelage occurs. Feet are large and robust, being light brown and well-furred dorsally. Claws are amber on forefeet and dull brown on hindfeet; pollux is extremely small. Ears are moderately long and brownish, with no hair internally. Tail is ¢.82-104% of head-body length and deep brownish drab, interspersed with visible white hair. Skull is large and robust, similarly to the Short-tailed Bandicoot Rat. Habitat. Marsh and swamp land. Food and Feeding. No information. Breeding. No information. Activity patterns. The Long-tailed Bandicoot Rat is terrestrial, although it isfound in swampy and marshy areas and is probably amphibious. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Endangered on The IUCN Red List. The Longtailed Bandicoot Rat is apparently rare and is known from very few specimens. Marsh and swamp habitats in which it is found were completely destroyed during the Iraq War by draining, war damage, and agricultural expansion. In recent years, flooding from Tigris and Euphrates rivers and high snow fall and melt haveresulted in partial restoration ofits native habitat, although restoration is not a complete. Populations are now probably highly fragmented. Bibliography. Al-Ansari et al. (2012), Al-Robaae & Felten (1990), Khajuria (1981), Krystufek et al. (2017), Musser & Carleton (2005), Richardson & Hussain (2006), Stuart (2008).
Deccan region, Madras, India. Genus Vandeleuria is masculine, so widely used specific name oleracea has been changed for gender agreement. Vandeleuria oleraceusis possibly a composite of species. Polytypic, but subspecific taxonomy requires reassessment. Distribution. Widespread in S Asia (India, Nepal, Bhutan, Bangladesh, and Sri Lan-ka), S China (W & S Yunnan), and mainland SE Asia N of the Isthmus of Kra. Descriptive notes. Head-body 68 mm, tail 105 mm, ear 13 mm, hindfoot 17 mm; weight 10 g. The Indomalayan Long-tailed Climbing Mouse is small, with flat nail on outer finger and outertoe; tail is slender, brown, twice as long as head-body length, and lacks distal tuft. Dorsal pelageis silky and salmon in color; venter is white, with fulvous hues. Habitat. Tall cane and tangled vines in primary and secondary forest such as bamboo forest, moist deciduous forest, temperate forests, montane wet zone, and disturbed secondary forests, and perhaps agricultural areas at elevations of 150-1500 m. Food and Feeding. Indomalayan [Long-tailed Climbing Mice eat fruits, buds, and flowers. Breeding. Litters of the Indomalayan Long-tailed Climbing Mouse have 3-6 young. Activity patterns. Indomalayan Long-tailed Climbing Mice are arboreal and nocturnal, although one individual was caught duringthe day. Movements, Home range and Social organization. Indomalayan Long-tailed Climbing Mice build nests in tall bushes or cane to rear their young. Status and Conservation. Classified as Least Concern on The IUCN Red Last (as V. olacea). The Indomalayan Long-tailed Climbing Mouse occurs in several habitats and a wide distribution that includes national parks. Further taxonomical studies are required to assess conservation status ofthis potentially diverse species complex. Bibliography. Corbet & Hill (1992), Dang Huy Huynh et al. (1994), Ellerman (1941), Marshall (1977b), Musser & Carleton (2005), Osgood (1932), Phillips (1980), Wang Yingxiang (2003). in Muridae
Deccan region, Madras, India. Genus Vandeleuria is masculine, so widely used specific name oleracea has been changed for gender agreement. Vandeleuria oleraceusis possibly a composite of species. Polytypic, but subspecific taxonomy requires reassessment. Distribution. Widespread in S Asia (India, Nepal, Bhutan, Bangladesh, and Sri Lan-ka), S China (W & S Yunnan), and mainland SE Asia N of the Isthmus of Kra. Descriptive notes. Head-body 68 mm, tail 105 mm, ear 13 mm, hindfoot 17 mm; weight 10 g. The Indomalayan Long-tailed Climbing Mouse is small, with flat nail on outer finger and outertoe; tail is slender, brown, twice as long as head-body length, and lacks distal tuft. Dorsal pelageis silky and salmon in color; venter is white, with fulvous hues. Habitat. Tall cane and tangled vines in primary and secondary forest such as bamboo forest, moist deciduous forest, temperate forests, montane wet zone, and disturbed secondary forests, and perhaps agricultural areas at elevations of 150-1500 m. Food and Feeding. Indomalayan [Long-tailed Climbing Mice eat fruits, buds, and flowers. Breeding. Litters of the Indomalayan Long-tailed Climbing Mouse have 3-6 young. Activity patterns. Indomalayan Long-tailed Climbing Mice are arboreal and nocturnal, although one individual was caught duringthe day. Movements, Home range and Social organization. Indomalayan Long-tailed Climbing Mice build nests in tall bushes or cane to rear their young. Status and Conservation. Classified as Least Concern on The IUCN Red Last (as V. olacea). The Indomalayan Long-tailed Climbing Mouse occurs in several habitats and a wide distribution that includes national parks. Further taxonomical studies are required to assess conservation status ofthis potentially diverse species complex. Bibliography. Corbet & Hill (1992), Dang Huy Huynh et al. (1994), Ellerman (1941), Marshall (1977b), Musser & Carleton (2005), Osgood (1932), Phillips (1980), Wang Yingxiang (2003).
FIGURE 6. Senecio ephemerus J. Calvo & Saldivia. A. Individual plant. B. Involucral bracts. C. Ray floret. D in Taxonomic and nomenclatural notes on Chilean Senecio (Asteraceae, Senecioneae), including a new particular species
FIGURE 6. Senecio ephemerus J. Calvo & Saldivia. A. Individual plant. B. Involucral bracts. C. Ray floret. D. Disc floret [Scale bars: A = 5 mm, B–D = 2 mm; pictures from the type material].
Deaf individuals use compensatory strategies to estimate visual time events
<p>Dataset related to the manuscript entitled Deaf individuals use compensatory strategies to estimate visual time events</p>
Coordinates and SSR data of Betula humilis individuals
<p>The file contains coordinates and microsatellite data of the shrub birch <em>(Betula humilis) </em>individuals from three Polish populations collected for the study of genetic diversity and fine-scale spatial genetic structure.</p>
FIGURE 2. Rainieria tenebrosa, live individuals. A in New records of Micropezidae (Diptera, Acalyptratae) from South Korea, with description of a new species of Rainieria Rondani
FIGURE 2. Rainieria tenebrosa, live individuals. A, female; B, male; C, mating pair, with smaller male; D, mating pair, with smaller female; E, bubbling behavior of female during copulation; F, fluid exchange during copulation; G, male waving the intruder away during copulation; H, 'aggregation oviposition' on a bark of Quercus cf. dentata Thunb. [Figure D provided by Jae Seok Oh (SNU)]
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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.