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63 results for “tails of distribution”
Figure 3 in Distribution and roosting ecology of the lesser mouse-tailed bat, Rhinopoma hardwickii Gray, 1831 (Chiroptera: Rhinopomatidae)
Figure 3. Map shows the distribution of lesser mouse-tailed bat, Rhinopoma hardwickii. The locations of roost sites were abbreviated and shown in the map: 1) AGC – Agra, 2) SFA – Sangam Fort (Allahabad), 3) NTB – Neelkanth Temple Kalinjar (Banda), 4) BAC – Banda, 5) PKC – Purani kotwali (Chitrakoot), 6) AFE – Awagdh Fort (Etah), 7) FBC – Faizabad, 8) FPC – Fatehpur, 9) EPF – Edalpur (Firozabad), 10) JFJ– Jaunpur Fort (Jaunpur), 11) BMJ – Bukhara, Mauranipur (Jhansi), 12) JHC – Jhansi, 13) LPC – Lalitpur, 14) TFL – Talbahte Fort (Lalitpur), 15) KKL – Kakori (Lucknow), 16) TTM– Tirthankar Temple (Mahowa), 17) MFM – Mirzapur Fort (Mirzapur), 18) KBP – Khusaroo bagh, 19) RBC – Raebareli, 20) SPC – Sultanpur, 21) UNC – Unnao.
Рис. 2. РаспреΑеΛение трубконосых птиц (А — темноспинный аΛьбатрос, Б — гΛупыш, В — тонкокΛювый буревестник, Г — сизая качурка) в Охотском море и сопреΑеΛьных воΑах Тихого океана и Японского моря по резуΛьтатам суΑовых учетов в февраΛе — мае 2020 г. (особей/км2 на 10-минутных трансектах). СпΛошными Λиниями показаны учетные трансекты, пунктиром — 200-метровая изобата Fig. 2. Distribution of tubenoses — (А) Laysan albatross, (Б) Northern fulmar, (В) shorttailed shearwater, (Г) fork-tailed storm-petrel — in the Sea of Okhotsk and adjacent waters of the Pacific Ocean and the Sea of Japan in February–May 2020 (birds/km2 on 10-minute transects). Solid lines indicate transects; dotted line indicates a 200 m isobath in Population of seabirds in the Sea of Okhotsk and adjacent waters of the Pacific Ocean and the Sea of Japan during the winter-spring period of 2020
Рис. 2. РаспреΑеΛение трубконосых птиц (А — темноспинный аΛьбатрос, Б — гΛупыш, В — тонкокΛювый буревестник, Г — сизая качурка) в Охотском море и сопреΑеΛьных воΑах Тихого океана и Японского моря по резуΛьтатам суΑовых учетов в февраΛе — мае 2020 г. (особей/км2 на 10-минутных трансектах). СпΛошными Λиниями показаны учетные трансекты, пунктиром — 200-метровая изобата Fig. 2. Distribution of tubenoses — (А) Laysan albatross, (Б) Northern fulmar, (В) shorttailed shearwater, (Г) fork-tailed storm-petrel — in the Sea of Okhotsk and adjacent waters of the Pacific Ocean and the Sea of Japan in February–May 2020 (birds/km2 on 10-minute transects). Solid lines indicate transects; dotted line indicates a 200 m isobath
Figure 4 in Ensemble distribution modeling of the Mesopotamian spiny-tailed lizard, Saara loricata (Blanford, 1874), in Iran: an insight into the impact of climate change
Figure 4. Overlay of Iranian Conservation Network with the habitat suitability map of the Mesopotamian spiny-tailed lizard.
Figure 3 in Ensemble distribution modeling of the Mesopotamian spiny-tailed lizard, Saara loricata (Blanford, 1874), in Iran: an insight into the impact of climate change
Figure 3. Model of habitat suitability for the species based on the present climatic data (A) and 2.6 (B) and 8.5 (C) scenarios of the CCSM for the future.
Figure 1 in Ensemble distribution modeling of the Mesopotamian spiny-tailed lizard, Saara loricata (Blanford, 1874), in Iran: an insight into the impact of climate change
Figure 1. The presence records (black dots) used for the development of a maximum entropy model for predicting the habitat suitability of the Mesopotamian spiny-tailed lizard.
Expanded distribution and predicted suitable habitat for the critically endangered yellow-tailed woolly monkey (Lagothrix flavicauda) in Peru
<p><span>The Tropical Andes Biodiversity Hotspot holds a remarkable number of species at risk of extinction due to anthropogenic habitat loss, hunting and climate change. One of these species, the Critically Endangered yellow-tailed woolly monkey (<em>Lagothrix flavicauda</em>), was recently sighted in Junín region, 206 kilometres south of its previously known distribution. The range extension, combined with continued habitat loss, calls for a re-evaluation of the species' distribution and available suitable habitat. Here, we present novel data from surveys at 53 sites in the regions of Junín, Cerro de Pasco, Ayacucho and Cusco. We encountered <em>L. flavicauda </em>at 9 sites, all in Junín, and the congeneric <em>L. l. tschudii</em> at 20 sites, but never in sympatry. Using these new localities along with all previous geographic localities for the species, we made predictive Species Distribution Models based on Ecological Niche Modelling using a generalized linear model and maximum entropy. Each model incorporated bioclimatic variables, forest cover, vegetation measurements, and elevation as predictor variables. Model evaluation showed >80% accuracy for all measures. Precipitation was the strongest predicter of species presence. Habitat suitability maps illustrate potential corridors for gene flow between the southern and northern populations, although much of this area is inhabited by <em>L. l. tschudii</em>. An analysis of the current protected area (PA) network showed ~47% of remaining suitable habitat is unprotected. With this, we suggest priority areas for new protected areas or expansions to existing reserves that would conserve potential corridors between <em>L. flavicauda</em> populations. Further surveys and characterization of the distribution in intermediate areas, combined with studies on genetic flow, are still needed to protect this species.</span></p>
Expanded distribution and predicted suitable habitat for the critically endangered yellow-tailed woolly monkey (Lagothrix flavicauda) in Peru
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Figure 2 in Distribution and roosting ecology of the lesser mouse-tailed bat, Rhinopoma hardwickii Gray, 1831 (Chiroptera: Rhinopomatidae)
Figure 2. The fatty abdominal tissue of Rhinopoma hardwickii.
Figure 1 in Distribution and roosting ecology of the lesser mouse-tailed bat, Rhinopoma hardwickii Gray, 1831 (Chiroptera: Rhinopomatidae)
Figure 1. The lesser mouse-tailed bat, Rhinopoma hardwickii.
Figure 21 in Breeding behavior, distribution, and conservation of the Sharp-tailed Tyrant Culicivora caudacuta (Vieillot, 1818) (Aves: Tyrannidae), a South American grassland specialist
Figure 21. Records of Culicivora caudacuta. Yellow stars indicate museum specimens, dots indicate other categories of records. See Appendix 1 for details.
Figure 22 in Breeding behavior, distribution, and conservation of the Sharp-tailed Tyrant Culicivora caudacuta (Vieillot, 1818) (Aves: Tyrannidae), a South American grassland specialist
Figure 22. Culicivora caudacuta habitat occupation by Eucalyptus sp. monoculture, Araxá, Ribeirão do Inferno (07 May 2014). Photo: RSS.
Figure 1 in Breeding behavior, distribution, and conservation of the Sharp-tailed Tyrant Culicivora caudacuta (Vieillot, 1818) (Aves: Tyrannidae), a South American grassland specialist
Figure 1. Adult Sharp-tailed Tyrant Culicivora caudacuta, (11 October 2011), Patrocínio, Minas Gerais, Brazil. Photo: RSS.
Figure 20 in Breeding behavior, distribution, and conservation of the Sharp-tailed Tyrant Culicivora caudacuta (Vieillot, 1818) (Aves: Tyrannidae), a South American grassland specialist
Figure 20. Specimen of young Culicivora caudacuta at Zoologische Staatssammlung München. Photo: Markus Unsöld.
Plate 1 in Population status and distribution assessment of Nicobar Long-Tailed Macaque Macaca Fascicularis Umbrosus (Miller, 1902) in Nicobar Group of Islands
Plate 1. Nicobar Long tailed Macaque in its natural forested habitat.
Figure 2 in Ensemble distribution modeling of the Mesopotamian spiny-tailed lizard, Saara loricata (Blanford, 1874), in Iran: an insight into the impact of climate change
Figure 2. The habitat suitability map of the Mesopotamian spiny-tailed lizard in southwestern Iran.
Data from: Genetic variation and structure in contrasting geographic distributions: widespread vs. restricted black-tailed prairie dogs (subgenus Cynomys)
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Data from: A revision to the distribution of plumage polymorphism in the Red-tailed Hawk (Buteo jamaicensis)
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Distribution. Angola, DR Congo, Malawi, Mozambique, Tanzania, and Zambia. Description. Head-body 46:5-47-8 cm (males), 44-45-5 cm (females), tail 40-43 cm (males), 38-39 cm (females), hindfoot 8:7-9-8 cm (males), 8-9 cm (females), ear 4-7-5-4 cm (males), 5-1-5-8 cm (females); weight 1-3-2 kg. The coat color is pale ocher, with brownish or grayish tones; melanistic individuals are quite common. The throat and chest are blackish, and the ventral pelage varies from creamy white to dirty white. The stripes and spots on the body vary from different hues of brown to black. The nuchal stripes run as two parallel lines from the nape to the shoulders, where they diverge and enlarge towards the elbows; they are not so conspicuously marked as in other genet species. Below them, a pair of thinner stripes and small spots are scattered on the shoulders and sides of the neck. A third pair of thinner, parallel stripes runs down the neck between the nuchal stripes, extending to about one fourth of the mid-dorsal line, where they vanish or diverge as the first row of flank spots. The black mid-dorsal line is continuous and is flanked on each side by four rows of oblong to squared spots, and by a few small-scattered spots below. There is a dorsal erectile crest. The face has a dark mask and a pair of white sub-ocular spots. The tail has seven to nine black rings, alternating with pale rings; the intervening white spaces are pigmented with a brownish tinge on the dorsal midline. The width of the pale rings relative to the dark rings in the middle of the tail is 50-75%; the tip of the tail is dark. The hindlimbs and forelimbs are black; there are white hairs on the metacarpals and metatarsals. [he posterior parts of the feet are dark. There are two pairs of teats. The posterior chamber of the auditory bulla is not ventrally inflated and has a continuous curve line on the external side. The ratio between the inter-orbital constriction and frontal width is 1-00 + 0-12. Dental formula: 13/3, C1/1,P 4/4, M 2/2 = 40. in Viverridae
Distribution. Angola, DR Congo, Malawi, Mozambique, Tanzania, and Zambia. Description. Head-body 46:5-47-8 cm (males), 44-45-5 cm (females), tail 40-43 cm (males), 38-39 cm (females), hindfoot 8:7-9-8 cm (males), 8-9 cm (females), ear 4-7-5-4 cm (males), 5-1-5-8 cm (females); weight 1-3-2 kg. The coat color is pale ocher, with brownish or grayish tones; melanistic individuals are quite common. The throat and chest are blackish, and the ventral pelage varies from creamy white to dirty white. The stripes and spots on the body vary from different hues of brown to black. The nuchal stripes run as two parallel lines from the nape to the shoulders, where they diverge and enlarge towards the elbows; they are not so conspicuously marked as in other genet species. Below them, a pair of thinner stripes and small spots are scattered on the shoulders and sides of the neck. A third pair of thinner, parallel stripes runs down the neck between the nuchal stripes, extending to about one fourth of the mid-dorsal line, where they vanish or diverge as the first row of flank spots. The black mid-dorsal line is continuous and is flanked on each side by four rows of oblong to squared spots, and by a few small-scattered spots below. There is a dorsal erectile crest. The face has a dark mask and a pair of white sub-ocular spots. The tail has seven to nine black rings, alternating with pale rings; the intervening white spaces are pigmented with a brownish tinge on the dorsal midline. The width of the pale rings relative to the dark rings in the middle of the tail is 50-75%; the tip of the tail is dark. The hindlimbs and forelimbs are black; there are white hairs on the metacarpals and metatarsals. [he posterior parts of the feet are dark. There are two pairs of teats. The posterior chamber of the auditory bulla is not ventrally inflated and has a continuous curve line on the external side. The ratio between the inter-orbital constriction and frontal width is 1-00 + 0-12. Dental formula: 13/3, C1/1,P 4/4, M 2/2 = 40.
Distribution. Brazilian Amazon along the right bank of the lower Rio Acari and through the interfluvium of the rios Acari (in the W) and Sucunduri (to the E), S perhaps to the distribution of the Black-tailed Marmoset (M. melanurus) between the rios Aripuana and Juruena. in Callitrichiade
Distribution. Brazilian Amazon along the right bank of the lower Rio Acari and through the interfluvium of the rios Acari (in the W) and Sucunduri (to the E), S perhaps to the distribution of the Black-tailed Marmoset (M. melanurus) between the rios Aripuana and Juruena.
Subspecies and Distribution. O.v.virginianusZimmermann,1780—fromVirginiatoMississippiandGeorgia. O.v.acapulcensisCaton,1877—coastalSCMexico. O.v.borealisMiller,1900-SECanadaandNEUSA. O.v.cariamuBoddaert.1784-FrenchGuianaandNEBrazil. O.v.carrnimlsGoldman8:Kellogg,1940-NMexico(CarmenMts,Coahuila). O.v.chiriquemisJ.A.Allen,1910-Panama. O.v.clamumBarbour&G.M.Allen,1922-SEUSA(HeridaKeys). O.v.couesiCoues8:Yarrow,1875fromNevada(SWUSA)toNWMexico. O.v.cumxsawhuHummelinck,1940-LesserAntilles(Curaçao1). O.v.dacolensısGoldman8:Kellogg,1940fromBritishColumbia8cAlberta(SWCanada)toColorado8cSDakota(NUSA). O.v.gnudoliiGay8cGervais,1846-C8:EColombia,WVenezuela,ÊEcuador,andNPeru. O.v.gymnotisWiegmann,1833fromEVenezuelatoSuriname. O.v.hillonmsisGoldman8:Kellogg,1940-SEUSA(HiltonHeadI,SouthCarolina). O.v.IeucumsDouglas,1829-NWUSA(CoastalWashington8cOregon). O.v.macmurusRafinesque,1817fromSMinnesotatoCLouisiana(USA). O.v.margarita:Osgood,1910-Venezuela(IslaMargarita). O.v.mcilhennyiEW.Miller,1928-SUSA(coastalTexas8:Louisiana). O.v.mexıcanusGmelin,1788-CMexico. O.v.miquihuanensisGoldman8cKellogg,1940-NCMexico. O.v.nelsoniMerriam,1898-SMexico,Guatemala. O.v.rugribarbisGoldman8:Kellogg,1940-SEUSA(Blackbeardl.Georgia). O.v.oaxacensisGoldman8cKellogg,1940-SMexico(Oaxaca). O.v.ochrourusBailey,1932-SWCanadaandNWUSA(innerWashingtonandOregonioWyoming). O.v.muelaBangs,1896-SEUSA(NWFlorida). O.v.pmıvıanusGray,1874-PeruandNWBolivia. O.v.rothschildiThomas,1902-Panama(Coibal). O.v.semmalusGoldman&Kellogg,1940-SEUSA(Florida). O.v.smaloaeJ.AAllen,1903-CWMexico. O.v.launnsulaeGoldman8cKellogg,1940-EUä(Bulls1,NonlrCarolina). O.v.taranusMeams,1898-CUSA(fromNebraskatoNewMexicoandTexas). O.v.thomasiMerriam,1898-SEMexicoandGuatemala. O.v.loltecusSaussure,1860-SMexico. O.v.lmpualzsCabrera,1918coastalColombiaandEcuador. O.v.truerMerriam,1898fromBelizetoCostaRica. O.v.ustusTrouessart,1910innerEcuador. O.v.venalorıusGoldman8cKellogg,1940—EUSA(HuntingIs,SouthCarolina). O.v.vememıasGoldman8:Kellogg,1940—NEMexico. O. v. yuaıtanensıls Hays. 1872 -SE Mexico (Yucatan). White-tailed Deer have been introduced into Czech Republic, Finland, Serbia, New Zealand, and Cuba. in Cervidae
Subspecies and Distribution. O.v.virginianusZimmermann,1780—fromVirginiatoMississippiandGeorgia. O.v.acapulcensisCaton,1877—coastalSCMexico. O.v.borealisMiller,1900-SECanadaandNEUSA. O.v.cariamuBoddaert.1784-FrenchGuianaandNEBrazil. O.v.carrnimlsGoldman8:Kellogg,1940-NMexico(CarmenMts,Coahuila). O.v.chiriquemisJ.A.Allen,1910-Panama. O.v.clamumBarbour&G.M.Allen,1922-SEUSA(HeridaKeys). O.v.couesiCoues8:Yarrow,1875fromNevada(SWUSA)toNWMexico. O.v.cumxsawhuHummelinck,1940-LesserAntilles(Curaçao1). O.v.dacolensısGoldman8:Kellogg,1940fromBritishColumbia8cAlberta(SWCanada)toColorado8cSDakota(NUSA). O.v.gnudoliiGay8cGervais,1846-C8:EColombia,WVenezuela,ÊEcuador,andNPeru. O.v.gymnotisWiegmann,1833fromEVenezuelatoSuriname. O.v.hillonmsisGoldman8:Kellogg,1940-SEUSA(HiltonHeadI,SouthCarolina). O.v.IeucumsDouglas,1829-NWUSA(CoastalWashington8cOregon). O.v.macmurusRafinesque,1817fromSMinnesotatoCLouisiana(USA). O.v.margarita:Osgood,1910-Venezuela(IslaMargarita). O.v.mcilhennyiEW.Miller,1928-SUSA(coastalTexas8:Louisiana). O.v.mexıcanusGmelin,1788-CMexico. O.v.miquihuanensisGoldman8cKellogg,1940-NCMexico. O.v.nelsoniMerriam,1898-SMexico,Guatemala. O.v.rugribarbisGoldman8:Kellogg,1940-SEUSA(Blackbeardl.Georgia). O.v.oaxacensisGoldman8cKellogg,1940-SMexico(Oaxaca). O.v.ochrourusBailey,1932-SWCanadaandNWUSA(innerWashingtonandOregonioWyoming). O.v.muelaBangs,1896-SEUSA(NWFlorida). O.v.pmıvıanusGray,1874-PeruandNWBolivia. O.v.rothschildiThomas,1902-Panama(Coibal). O.v.semmalusGoldman&Kellogg,1940-SEUSA(Florida). O.v.smaloaeJ.AAllen,1903-CWMexico. O.v.launnsulaeGoldman8cKellogg,1940-EUä(Bulls1,NonlrCarolina). O.v.taranusMeams,1898-CUSA(fromNebraskatoNewMexicoandTexas). O.v.thomasiMerriam,1898-SEMexicoandGuatemala. O.v.loltecusSaussure,1860-SMexico. O.v.lmpualzsCabrera,1918coastalColombiaandEcuador. O.v.truerMerriam,1898fromBelizetoCostaRica. O.v.ustusTrouessart,1910innerEcuador. O.v.venalorıusGoldman8cKellogg,1940—EUSA(HuntingIs,SouthCarolina). O.v.vememıasGoldman8:Kellogg,1940—NEMexico. O. v. yuaıtanensıls Hays. 1872 -SE Mexico (Yucatan). White-tailed Deer have been introduced into Czech Republic, Finland, Serbia, New Zealand, and Cuba.
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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.