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58 results for “Desert area”
Subspecies and Distribution. S. s. scrofa Linnaeus, 1758 — W Europe, from Denmark, Germany, Poland, and Czech Republic to N Italy and N Iberian Peninsula; possibly also Albania. The taxonomic status of animals in Austria, Switzerland, Slovenia, and Slovakia is unclear but presumably these populations are included in scrofa, as are the populations of Sweden, Finland, and the Baltic states. However, restocking of once depleted populations, for example in Italy, has likely involved the introduction and mixing of this subspecies with other subspecies, such as attila. S. s. affinis Gray, 1847 — S India and Sri Lanka. S. s. algirus Loche, 1867 — Tunisia, Algeria, and Morocco, on the coastal side of the mountains or in the low montane areas. S. s. attila Thomas, 1912 — Hungary, Ukraine, C & S Belarus, Romania, Moldova, and S Russia towards the N flank of the Caucasus, but not including the Transcaucasian countries of Georgia, Armenia, and Azerbaijan. The range possibly extends as far S as the Mesopotamian Delta in Iraq, in which case it would likely include W & SW Iran, and possibly E Turkey and Syria, where it borders with lybicus. Such a range could not be easily reconciled with a statement by Groves that "the difference between pigs from N and S of the Caucasus is quite striking; Transcaucasian boars are certainly not attila." This subspecies may also extend into C Asia and include Kazakhstan, Uzbekistan, and Turkmenistan, but no data exist to support this. S. s. baeticus Thomas, 1912 — originally described from Coto Donana, S Spain, and later merged with meridionalis; also S Portugal. Unless evidence is found that these Italian and Iberian populations are the relics of a much larger formerly contiguous range, this subspecies should be kept as distinct. S. s. coreanus Heude, 1897 — Korean Peninsula. S. s. eristatus Wagner, 1839 — Himalayas S to C India and E to Indochina (N of the Kra Isthmus). S. s. davidi Groves, 1981 — the arid zone from E Iran to Gujarat, including Pakistan and NW India, and perhaps N to Tajikistan. S. s. leucomystax Temminck, 1842 — main Is ofJapan (Honshu, Shikoku, Kyushu, Nakadori, Hiburijima, Tojima, Kushima, and other smaller Is). S. s. lybicus Gray, 1868 — Bulgaria, Greece, Turkey, Syria, Jordan, Israel, Palestine, in the past also in Lybia, and Egypt. The former Yugoslavia was included in its range, which would suggest that now Slovenia, Serbia, Croatia, Bosnia and Herzegovina, Montenegro, and Kosovo are within the range of this subspecies, although the exact boundaries are unclear. Pigs from Albania have been assigned to S. s. scrofa. S. s. majori De Beaux & Festa, 1927 — C & S Italian Peninsula. S. s. menidionalis Forsyth Major, 1882 — Corsica and Sardinia, with the proviso that the two populations are very likely to be introduced or feral. S. s. moupinensis Milne-Edwards, 1871 — China, S to Vietnam and W to Sichuan. S. s. nigripes Blanford, 1875 — the flanks of the Tianshan mountains in Kyrgyzstan and NW China (Xinjiang). An animal photographed in NE Iran (Golestan) looked like this subspecies. S. s. nukiuanus Kuroda, 1924 — Iriomote, Ishigaki, Okinawa, Tokunoshima, Amamioshima, and Kakerome Is in the Ryukyu chain in extreme S Japan, though some of these populations have hybridized with introduced domesticates. S. s. sibiricus Staffe, 1922 — Mongolia and Transbaikal (S & E of Lake Baikal). S. s. tawvanus Swinhoe, 1863 — Taiwan. S. s. ussuricus Heude, 1888 — far E Russia and the Manchurian region (China). Korean populations were previously included in this subspecies, but based on new evidence, the Korean taxon seems more similar to moupinensis. S. s. vittatus Boie, 1828 — Malay Peninsula, S of the Isthmus of Kra, the offshore islands of Terutai and Langkawi, Sumatra, Riau Archipelago, Java, Bali, and a range of smaller islands around these, including Babi, Bakong, Batam, Bawean, Bengkalis, Bintan, Bulan, Bunguran, Cuyo, Deli, Durian, Enggano, Galang, Jambongan, Karimon (Riau Is), Kundur, Lagong, Laut, Lingga, Lingung, Mapor, Moro Kecil, North Pagai, Nias, Panaitan, Payong, Penang, Pinie, Rupat, Siantan, Siberut, Simeulue, Singkep, Sugi, Sugi Bawa, Telibon, Tinggi, Tuangku, and the Tambelan Is. This species was originally present from the British Is in the extreme W, through Eurasia from S Scandinavia to S Siberia, extending as far E as Korea and Japan, and SE into some of the Sunda Is and Taiwan. In the S the species ranged along the Nile Valley to Khartoum, and N of the Sahara in Africa, more orless following the continental coasts of S, E, and SE Asia. Within this range it was absent only from extremely dry deserts, e.g. the driest regions of Mongolia and in China W of Sichuan; and alpine zones, such as the high altitudes of Pamir and Tien Shan. In recent centuries, the range of S. scrofa has changed dramatically because of hunting and changes in available habitat. The species disappeared from the British Is in the 17" century, from Denmark in the 19" century, and was greatly reduced in range and numbers in the 20" century from areas as distant as Tunisia, Sudan, Germany, and Russia. Following these severe declines, there were some slight population recoveries in Russia, Italy, Spain, and Germany in the mid-20™ century, and natural and assisted range expansions in Denmark and Sweden. The species has also been inadvertently reintroduced in various locations in the Great Britain via escapees of mixed origin from commercial farming enterprises. Ex-S. scrofa stocks also occur as introduced feral populations in various other parts of the world, including Australia, New Zealand, the eastern Malay Archipelago, and in North, Central, and South America. In all of these areas they are now generally recognized as a major pest. in Suidae
Subspecies and Distribution. S. s. scrofa Linnaeus, 1758 — W Europe, from Denmark, Germany, Poland, and Czech Republic to N Italy and N Iberian Peninsula; possibly also Albania. The taxonomic status of animals in Austria, Switzerland, Slovenia, and Slovakia is unclear but presumably these populations are included in scrofa, as are the populations of Sweden, Finland, and the Baltic states. However, restocking of once depleted populations, for example in Italy, has likely involved the introduction and mixing of this subspecies with other subspecies, such as attila. S. s. affinis Gray, 1847 — S India and Sri Lanka. S. s. algirus Loche, 1867 — Tunisia, Algeria, and Morocco, on the coastal side of the mountains or in the low montane areas. S. s. attila Thomas, 1912 — Hungary, Ukraine, C & S Belarus, Romania, Moldova, and S Russia towards the N flank of the Caucasus, but not including the Transcaucasian countries of Georgia, Armenia, and Azerbaijan. The range possibly extends as far S as the Mesopotamian Delta in Iraq, in which case it would likely include W & SW Iran, and possibly E Turkey and Syria, where it borders with lybicus. Such a range could not be easily reconciled with a statement by Groves that "the difference between pigs from N and S of the Caucasus is quite striking; Transcaucasian boars are certainly not attila." This subspecies may also extend into C Asia and include Kazakhstan, Uzbekistan, and Turkmenistan, but no data exist to support this. S. s. baeticus Thomas, 1912 — originally described from Coto Donana, S Spain, and later merged with meridionalis; also S Portugal. Unless evidence is found that these Italian and Iberian populations are the relics of a much larger formerly contiguous range, this subspecies should be kept as distinct. S. s. coreanus Heude, 1897 — Korean Peninsula. S. s. eristatus Wagner, 1839 — Himalayas S to C India and E to Indochina (N of the Kra Isthmus). S. s. davidi Groves, 1981 — the arid zone from E Iran to Gujarat, including Pakistan and NW India, and perhaps N to Tajikistan. S. s. leucomystax Temminck, 1842 — main Is ofJapan (Honshu, Shikoku, Kyushu, Nakadori, Hiburijima, Tojima, Kushima, and other smaller Is). S. s. lybicus Gray, 1868 — Bulgaria, Greece, Turkey, Syria, Jordan, Israel, Palestine, in the past also in Lybia, and Egypt. The former Yugoslavia was included in its range, which would suggest that now Slovenia, Serbia, Croatia, Bosnia and Herzegovina, Montenegro, and Kosovo are within the range of this subspecies, although the exact boundaries are unclear. Pigs from Albania have been assigned to S. s. scrofa. S. s. majori De Beaux & Festa, 1927 — C & S Italian Peninsula. S. s. menidionalis Forsyth Major, 1882 — Corsica and Sardinia, with the proviso that the two populations are very likely to be introduced or feral. S. s. moupinensis Milne-Edwards, 1871 — China, S to Vietnam and W to Sichuan. S. s. nigripes Blanford, 1875 — the flanks of the Tianshan mountains in Kyrgyzstan and NW China (Xinjiang). An animal photographed in NE Iran (Golestan) looked like this subspecies. S. s. nukiuanus Kuroda, 1924 — Iriomote, Ishigaki, Okinawa, Tokunoshima, Amamioshima, and Kakerome Is in the Ryukyu chain in extreme S Japan, though some of these populations have hybridized with introduced domesticates. S. s. sibiricus Staffe, 1922 — Mongolia and Transbaikal (S & E of Lake Baikal). S. s. tawvanus Swinhoe, 1863 — Taiwan. S. s. ussuricus Heude, 1888 — far E Russia and the Manchurian region (China). Korean populations were previously included in this subspecies, but based on new evidence, the Korean taxon seems more similar to moupinensis. S. s. vittatus Boie, 1828 — Malay Peninsula, S of the Isthmus of Kra, the offshore islands of Terutai and Langkawi, Sumatra, Riau Archipelago, Java, Bali, and a range of smaller islands around these, including Babi, Bakong, Batam, Bawean, Bengkalis, Bintan, Bulan, Bunguran, Cuyo, Deli, Durian, Enggano, Galang, Jambongan, Karimon (Riau Is), Kundur, Lagong, Laut, Lingga, Lingung, Mapor, Moro Kecil, North Pagai, Nias, Panaitan, Payong, Penang, Pinie, Rupat, Siantan, Siberut, Simeulue, Singkep, Sugi, Sugi Bawa, Telibon, Tinggi, Tuangku, and the Tambelan Is. This species was originally present from the British Is in the extreme W, through Eurasia from S Scandinavia to S Siberia, extending as far E as Korea and Japan, and SE into some of the Sunda Is and Taiwan. In the S the species ranged along the Nile Valley to Khartoum, and N of the Sahara in Africa, more orless following the continental coasts of S, E, and SE Asia. Within this range it was absent only from extremely dry deserts, e.g. the driest regions of Mongolia and in China W of Sichuan; and alpine zones, such as the high altitudes of Pamir and Tien Shan. In recent centuries, the range of S. scrofa has changed dramatically because of hunting and changes in available habitat. The species disappeared from the British Is in the 17" century, from Denmark in the 19" century, and was greatly reduced in range and numbers in the 20" century from areas as distant as Tunisia, Sudan, Germany, and Russia. Following these severe declines, there were some slight population recoveries in Russia, Italy, Spain, and Germany in the mid-20™ century, and natural and assisted range expansions in Denmark and Sweden. The species has also been inadvertently reintroduced in various locations in the Great Britain via escapees of mixed origin from commercial farming enterprises. Ex-S. scrofa stocks also occur as introduced feral populations in various other parts of the world, including Australia, New Zealand, the eastern Malay Archipelago, and in North, Central, and South America. In all of these areas they are now generally recognized as a major pest.
Distribution. Most of Africa S of the Sahara Desert, except in lowland tropical rainforests. Spotted Hyenas have been extirpated from many areas of southern Africa. in Hyaenidae
Distribution. Most of Africa S of the Sahara Desert, except in lowland tropical rainforests. Spotted Hyenas have been extirpated from many areas of southern Africa.
Distribution. Sahelian savannas and desert areas from S Morocco, Western Sahara, Mauritania, and N Senegal E through Algeria, S Tunisia, Mali (N of Niger River), and Niger to C Libya and NW Chad. in Muridae
Distribution. Sahelian savannas and desert areas from S Morocco, Western Sahara, Mauritania, and N Senegal E through Algeria, S Tunisia, Mali (N of Niger River), and Niger to C Libya and NW Chad.
The dataset for water vapor research in margin of desert, arid and semi-arid area in northwestern China
<p>The dataset for water vapor research in margin of desert, arid and semi-arid area in northwestern China</p>
Vertebrate species composition of remnant desert islands within central Arizona-Phoenix urban areas: period 1998-1999
Urban growth around Phoenix over the last 30 years has produced numerous isolated "islands" of remnant desert habitat. Each of these remnants has its own unique vertebrate community, determined by the fauna present prior to isolation, area of remaining habitat, vegetation characteristics, time since isolation, and distance to other islands or source populations. These factors can be used as predictors of how future growth will affect potential desert preserves.
FIGURE. Map of the study area (Source: http://srtm.csi.cgiar.org) in Floristic diversity in Cold Desert regions of Uttarakhand Himalaya, India
FIGURE. Map of the study area (Source: http://srtm.csi.cgiar.org)
Fig. 5 in The Unnamed Plateau (Western Desert of Egypt). New geological and geoarchaeological data from an exploration in a remote area
Fig. 5 - Map illustrating the explored areas and the main points of interest (modified from Google Earth™). /La mappa illustra le aree esplorate e i punti d'interesse principali (modificata da Google Earth™).
Fig. 7 - A in The Unnamed Plateau (Western Desert of Egypt). New geological and geoarchaeological data from an exploration in a remote area
Fig. 7 - A) A stone circle of Area 2, along the edge of the plateau facing Wadi Handal. / Cerchio di pietre dell'Area 2 lungo il bordo dell'altopiano sovrastante Wadi Handal. B) Sandstone grinding stone. / Macina in arenaria.
Fig. 2 - A in The Unnamed Plateau (Western Desert of Egypt). New geological and geoarchaeological data from an exploration in a remote area
Fig. 2 - A) Clayton's map detail (1933) / Dettaglio della carta geografica di Clayton (1933). B) Geographic map of Egypt (Survey of Egypt, 1942). / Carta geografica dell'Egitto (Survey of Egypt, 1942). C) Geological map of Egypt (Conoco Coral & Egyptian General Petroleum Corporation, 1987). / Carta geologica dell'Egitto (Conoco Coral & Egyptian General Petroleum Corporation, 1987).
Fig. 11 - Area 4 in The Unnamed Plateau (Western Desert of Egypt). New geological and geoarchaeological data from an exploration in a remote area
Fig. 11 - Area 4. Pottery sherds / Frammenti di ceramica. A) Wavy-line impressions. / Decorazione a impressioni di linee ondulate. B) Packed dotted zig-zag. / Decorazione con impressioni a zigzag puntinati serrati. C) Rocker packed dotted zigzag zonal and unpatterned. / Impressioni puntinate a zigzag a pettine oscillante zonate e sparse. D) Unpatterned stripe incisions. /Incisioni a strisce irregolari. E) Plant-tempered vessel, with the outer surface smoothed after decoration with horizontal packed dotted zig-zag bands. / Recipiente a degrassante vegetale con superficie esterna lisciata dopo decorazione a zigzag puntinati serrati, in bande orizzontali. G) Thick-walled vessel decorated with scratches after smoothing. / Recipiente a pareti spesse decorato con graffiatura dopo essere stato lisciato. Other artifacts / Altri manufatti: F) A bone spatula. / Spatola in osso. H) Set of small stone balls. / Dotazione di palline in pietra. I-M) Laminar industry. / Industria laminare.
Figure 7 from: Homziak NT, Lightfoot DC, Metzler EH, Miller KB (2021) The Lepidoptera of Cuatrociénegas Protected Area 1. A new species in the genus Callistege Hübner, [1823] (Erebidae, Erebinae, Euclidiini) from the Chihuahuan Desert, Coahuila, Mexico. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 783-796. https://doi.org/10.3897/zookeys.1044.59773
Figure 7 Callistege triangula female genitalia. JGF slide number 6534. John. G. Franclemont Slide Collection, Cornell University. Scale bar: 2 mm.
Figure 6 from: Homziak NT, Lightfoot DC, Metzler EH, Miller KB (2021) The Lepidoptera of Cuatrociénegas Protected Area 1. A new species in the genus Callistege Hübner, [1823] (Erebidae, Erebinae, Euclidiini) from the Chihuahuan Desert, Coahuila, Mexico. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 783-796. https://doi.org/10.3897/zookeys.1044.59773
Figure 6 Callistege triangula male genitalia. JGF slide number 6533. John G. Franclemont Slide Collection, Cornell University. Scale bar: 1 mm.
Figure 5 from: Homziak NT, Lightfoot DC, Metzler EH, Miller KB (2021) The Lepidoptera of Cuatrociénegas Protected Area 1. A new species in the genus Callistege Hübner, [1823] (Erebidae, Erebinae, Euclidiini) from the Chihuahuan Desert, Coahuila, Mexico. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 783-796. https://doi.org/10.3897/zookeys.1044.59773
Figure 5 Callistege clara Homziak & Metzler, sp. nov. Mexico, Cuatrociénegas (paratype), female genitalia. Slide E.H.M. 587 (USNM). Scale bar: 2 mm.
Figure 4 from: Homziak NT, Lightfoot DC, Metzler EH, Miller KB (2021) The Lepidoptera of Cuatrociénegas Protected Area 1. A new species in the genus Callistege Hübner, [1823] (Erebidae, Erebinae, Euclidiini) from the Chihuahuan Desert, Coahuila, Mexico. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 783-796. https://doi.org/10.3897/zookeys.1044.59773
Figure 4 Callistege clara Homziak & Metzler, sp. nov. Mexico, Cuatrociénegas (paratype), aedeagus. Slide E.H.M. 586 (USNM). Scale bar: 1 mm.
Figure 3 from: Homziak NT, Lightfoot DC, Metzler EH, Miller KB (2021) The Lepidoptera of Cuatrociénegas Protected Area 1. A new species in the genus Callistege Hübner, [1823] (Erebidae, Erebinae, Euclidiini) from the Chihuahuan Desert, Coahuila, Mexico. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 783-796. https://doi.org/10.3897/zookeys.1044.59773
Figure 3 Callistege clara Homziak & Metzler, sp. nov. Mexico, Cuatrociénegas (paratype), male genitalia. Slide E.H.M. 585 (USNM). Scale bar: 1 mm.
Figure 2 from: Homziak NT, Lightfoot DC, Metzler EH, Miller KB (2021) The Lepidoptera of Cuatrociénegas Protected Area 1. A new species in the genus Callistege Hübner, [1823] (Erebidae, Erebinae, Euclidiini) from the Chihuahuan Desert, Coahuila, Mexico. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 783-796. https://doi.org/10.3897/zookeys.1044.59773
Figure 2 Callistege clara Homziak & Metzler, sp. nov., female (paratype). Mexico, Cuatrociénegas (MSBA 72903). Scale bar: 10 mm.
Figure 1 from: Homziak NT, Lightfoot DC, Metzler EH, Miller KB (2021) The Lepidoptera of Cuatrociénegas Protected Area 1. A new species in the genus Callistege Hübner, [1823] (Erebidae, Erebinae, Euclidiini) from the Chihuahuan Desert, Coahuila, Mexico. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 783-796. https://doi.org/10.3897/zookeys.1044.59773
Figure 1 Callistege clara Homziak & Metzler, sp. nov., male (holotype). Mexico, Cuatrociénegas (MSBA 72901). Scale bar: 10 mm.
Distribution. Endemic to W & C Australia, occurs in semiarid Gibson Desert, Pilbara, and Murchison regions of Western Australia, Northern Territory, extreme NW Queensland, and South Australia; one specimen is known from an outlying area in the Great Sandy Desert. in Emballonuridae
Distribution. Endemic to W & C Australia, occurs in semiarid Gibson Desert, Pilbara, and Murchison regions of Western Australia, Northern Territory, extreme NW Queensland, and South Australia; one specimen is known from an outlying area in the Great Sandy Desert.
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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.