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666 results for “type locality”
Distribution. Endemic to S India (Kolar district, Karnataka), known only from type locality. Previously also on nearby Therahalli, where now absent. in Hipposideridae
Distribution. Endemic to S India (Kolar district, Karnataka), known only from type locality. Previously also on nearby Therahalli, where now absent.
Distribution. Endemic to Laos, known only from type locality and Ban Nampe, C.I1 km NE of Vang Vieng, Vang Vieng district, Vientiane Province in Hipposideridae
Distribution. Endemic to Laos, known only from type locality and Ban Nampe, C.I1 km NE of Vang Vieng, Vang Vieng district, Vientiane Province
FIGURE 4 in Avian type localities and the type specimens collected by Johan August Wahlberg in southern Africa
FIGURE 4. Wahlberg's route in 1843 (red dots) across the Free State from the Drakensberg Mountains at Bezuidenhout's Pass to Potchefstroom via Skandinawiedrif across the Vaal River.
FIGURE 2 in Avian type localities and the type specimens collected by Johan August Wahlberg in southern Africa
FIGURE 2. Sundevall's personal acquisition catalogue, in which he recorded the date of the lectotype of Megalaema bilineata Sundevall as 4 November 1842.
FIGURE 1 in Avian type localities and the type specimens collected by Johan August Wahlberg in southern Africa
FIGURE 1. (A) An example of Wahlberg's handwriting; (B) a label on a Wahlberg specimen in what appears to be Sundevall's handwriting; (C) Sundevall's register with details of the type of Megalaema leucotis Sundevall; and (D) one of the few labels by Wahlberg's hand. The "Mr Hodgson" on (D) was the Rev. Mr. Thomas Laiman Hodgson (1787–1850), chairman of the Wesleyan church in the Cape district, who contributed several specimens of mammals, birds and reptiles to Wahlberg's collection.
Distribution. Recorded from six disjunct locations in SW & NE India and NE Cambodia, including type locality in Karnataka, and Phrang Karuh Cave, Jaintia Hills, and Thangsah in Meghalaya; in Cambodia known only from a single specimen from Chhaeb district, Preah Vihear Province, while another record based on a photograph of a dead bat from Bahon Temple is also provisionally referred to this species. in Molossidae
Distribution. Recorded from six disjunct locations in SW & NE India and NE Cambodia, including type locality in Karnataka, and Phrang Karuh Cave, Jaintia Hills, and Thangsah in Meghalaya; in Cambodia known only from a single specimen from Chhaeb district, Preah Vihear Province, while another record based on a photograph of a dead bat from Bahon Temple is also provisionally referred to this species.
Distribution. NW Argentina (Catamarca), known only from the type locality, Sierra de Ambato, about 18 km NNW Chumbicha. in Abrocomidae
Distribution. NW Argentina (Catamarca), known only from the type locality, Sierra de Ambato, about 18 km NNW Chumbicha.
Distribution. CW Argentina (N Neuquén Province), known only from the type locality and neighboring areas in the Chos Malal Department. in Ctenomyidae
Distribution. CW Argentina (N Neuquén Province), known only from the type locality and neighboring areas in the Chos Malal Department.
Distribution. NW Argentina (SW Catamarca Province), known only from the vicinity ofthe type locality. in Ctenomyidae
Distribution. NW Argentina (SW Catamarca Province), known only from the vicinity ofthe type locality.
Distribution. NW Argentina (La Rioja Province), occurs at the type locality and probably nearby areas, in Sierra de Famatina, reaching elevations up to 3800 m. in Ctenomyidae
Distribution. NW Argentina (La Rioja Province), occurs at the type locality and probably nearby areas, in Sierra de Famatina, reaching elevations up to 3800 m.
Distribution. NW Argentina (N Tucuman Province), known only from the type locality and neighboring areas. in Ctenomyidae
Distribution. NW Argentina (N Tucuman Province), known only from the type locality and neighboring areas.
Distribution. CS Bolivia, known only from the type locality at Cerro Itahuaticua at 800-1800 m altitude. in Ctenomyidae
Distribution. CS Bolivia, known only from the type locality at Cerro Itahuaticua at 800-1800 m altitude.
Distribution. SW Brazil, known only from two sites, the type locality in Rondonia and Juruena (Mato Grosso State)Descriptive notes Head-body ¢.230 mm, tail ¢.80 mm. No specific data are available for body weight. Rondon's Tuco-tuco is medium-sized. Dorsal hairs are pale at bases and sepia at tips. Head and venterare slightly rufous, and tail is uniform brown. Skull is robust and depressed. Inter-maxillaries are also robust, with lateral protruding expansion; maxillaries are narrow; and mandible is strong and wide. Supraorbital process protrudes, and traverse occipital-temporal crest is straight. Bullae are inflated. in Ctenomyidae
Distribution. SW Brazil, known only from two sites, the type locality in Rondonia and Juruena (Mato Grosso State)Descriptive notes Head-body ¢.230 mm, tail ¢.80 mm. No specific data are available for body weight. Rondon's Tuco-tuco is medium-sized. Dorsal hairs are pale at bases and sepia at tips. Head and venterare slightly rufous, and tail is uniform brown. Skull is robust and depressed. Inter-maxillaries are also robust, with lateral protruding expansion; maxillaries are narrow; and mandible is strong and wide. Supraorbital process protrudes, and traverse occipital-temporal crest is straight. Bullae are inflated.
FIGURE. Sanicula orthacantha in the wild (China, Chongqing, Nanchuan, Jinfo Shan, the type locality of S. nanchuanensis). A. Habitat. B. Habit. C. Leaves (left: adaxial surface; right: abaxial surface). D. Portion of inflorescence (side view). E. Portion of inflorescence (top view). F. Involucrate bracts. G. Umbellule (side view), a) involucellate bracteoles, b) calyx teeth. H. Staminate flowers (side view). I. Fertile flower with fruit. J. Mericarps. in Taxonomic studies on the genus Sanicula (Apiaceae) from China ( ): The clarification of some morphological distinction between S. orthacantha var. orthacantha and S. orthacantha var. brevispina, with the reduction of S. petagnioides to the synonymy of the former, and S. orthacantha var. stolonifera to
FIGURE. Sanicula orthacantha in the wild (China, Chongqing, Nanchuan, Jinfo Shan, the type locality of S. nanchuanensis). A. Habitat. B. Habit. C. Leaves (left: adaxial surface; right: abaxial surface). D. Portion of inflorescence (side view). E. Portion of inflorescence (top view). F. Involucrate bracts. G. Umbellule (side view), a) involucellate bracteoles, b) calyx teeth. H. Staminate flowers (side view). I. Fertile flower with fruit. J. Mericarps.
FIGURE. Sanicula orthacantha in the wild (China, Jiangxi, Jiujiang, Lushan, the type locality of S. orthacantha). A. Habitat. B. Habit. C. Leaves (left: adaxial surface; right: abaxial surface). D. Portion of inflorescence (side view). E. Portion of inflorescence (top view). F. Involucrate bracts. G. Umbellule (side view), a) involucellate bracteoles, b) calyx teeth. H. Staminate flowers (side view). I. Fertile flower with fruit, style, petals and calyx teeth. J. Mericarps in Taxonomic studies on the genus Sanicula (Apiaceae) from China ( ): The clarification of some morphological distinction between S. orthacantha var. orthacantha and S. orthacantha var. brevispina, with the reduction of S. petagnioides to the synonymy of the former, and S. orthacantha var. stolonifera to
FIGURE. Sanicula orthacantha in the wild (China, Jiangxi, Jiujiang, Lushan, the type locality of S. orthacantha). A. Habitat. B. Habit. C. Leaves (left: adaxial surface; right: abaxial surface). D. Portion of inflorescence (side view). E. Portion of inflorescence (top view). F. Involucrate bracts. G. Umbellule (side view), a) involucellate bracteoles, b) calyx teeth. H. Staminate flowers (side view). I. Fertile flower with fruit, style, petals and calyx teeth. J. Mericarps
FIGURE. Sanicula orthacantha var. brevispina in the wild (China, Sichuan, Emei Shan, the type locality of S. orthacantha var. brevispina and S. orthacantha var. stolonifera). A. Habitat and habit. B. Rhizome. C. Leaves (left: adaxial surface; right: abaxial surface). D. Portion of inflorescence (side view). E. Portion of inflorescence (top view). F. Involucrate bracts. G. Umbellule (side view), a) involucellate bracteoles, b) calyx teeth. H. Staminate flowers (side view). I. Fertile flower with fruit, style, petals and calyx teeth. J. Mericarps. in Taxonomic studies on the genus Sanicula (Apiaceae) from China ( ): The clarification of some morphological distinction between S. orthacantha var. orthacantha and S. orthacantha var. brevispina, with the reduction of S. petagnioides to the synonymy of the former, and S. orthacantha var. stolonifera to
FIGURE. Sanicula orthacantha var. brevispina in the wild (China, Sichuan, Emei Shan, the type locality of S. orthacantha var. brevispina and S. orthacantha var. stolonifera). A. Habitat and habit. B. Rhizome. C. Leaves (left: adaxial surface; right: abaxial surface). D. Portion of inflorescence (side view). E. Portion of inflorescence (top view). F. Involucrate bracts. G. Umbellule (side view), a) involucellate bracteoles, b) calyx teeth. H. Staminate flowers (side view). I. Fertile flower with fruit, style, petals and calyx teeth. J. Mericarps.
Distribution. SC China, known only from the type locality in Wanglang Nature Reserve, Pingwu County, N Sichuan Province. Distributional limits are not known. in Gliridae
Distribution. SC China, known only from the type locality in Wanglang Nature Reserve, Pingwu County, N Sichuan Province. Distributional limits are not known.
Subspecies and Distribution. P. l. longimembris Coues, 1875 — SW USA (Mojave Desert and Transverse Ranges, SW California). P. l. aestivus Huey, 1928 — NW Mexico (W base Sierra Juarez to Valle de la Trinidad, N Baja California). P.l. arizonensis Goldman, 1931 — SW USA (SC Utah and NC Arizona to SE Nevada). P. l.bangsi Mearns, 1898 — SW USA (W Colorado Desert of S California). P. l. bombycinus Osgood, 1907 — SW USA and NW Mexico (lower Colorado River Valley of SE California, SW Arizona, NE Baja California, and NW Sonora). P. l. brevinasus Osgood, 1900 — SW USA (arid coastal basins of SW California). P. l. gulosus Hall, 1941 — W USA (along the W margin of former Pleistocene Lake Bonneville in the Great Basin of E Nevada and W Utah). P. l. internationalis Huey, 1939 — SW USA and NW Mexico (SC California and adjacent NC Baja California). P. l. kinoensis Huey, 1935 — NW Mexico (disjunct and geographically restricted population along Bahia Kino, W Sonora), but may be extinct. P. l. nevadensis Merriam, 1894 — W USA (Great Basin of SE Oregon, NE California, and NC Nevada). P. l. pacificus Mearns, 1898 — SW USA (coastal plains of SW California to the USA-Mexico border). P. I. panamintinus Merriam, 1894 — SW USA (Great Basin of W Nevada and SE California). P. l. pimensis Huey, 1937 — SW USA (disjunct distribution in SC Arizona). P. l. salinensis Bole, 1937 — SW USA (restricted distribution in the Salinas Valley of SE California). P. l. tularensis Richardson, 1937 — SW USA (restricted distribution in the upper valley of the Kern River, SC California). P. l. venustus Huey, 1930 — NW Mexico (known only from the type locality of San Agustin, NC Baja California). in Heteromyidae
Subspecies and Distribution. P. l. longimembris Coues, 1875 — SW USA (Mojave Desert and Transverse Ranges, SW California). P. l. aestivus Huey, 1928 — NW Mexico (W base Sierra Juarez to Valle de la Trinidad, N Baja California). P.l. arizonensis Goldman, 1931 — SW USA (SC Utah and NC Arizona to SE Nevada). P. l.bangsi Mearns, 1898 — SW USA (W Colorado Desert of S California). P. l. bombycinus Osgood, 1907 — SW USA and NW Mexico (lower Colorado River Valley of SE California, SW Arizona, NE Baja California, and NW Sonora). P. l. brevinasus Osgood, 1900 — SW USA (arid coastal basins of SW California). P. l. gulosus Hall, 1941 — W USA (along the W margin of former Pleistocene Lake Bonneville in the Great Basin of E Nevada and W Utah). P. l. internationalis Huey, 1939 — SW USA and NW Mexico (SC California and adjacent NC Baja California). P. l. kinoensis Huey, 1935 — NW Mexico (disjunct and geographically restricted population along Bahia Kino, W Sonora), but may be extinct. P. l. nevadensis Merriam, 1894 — W USA (Great Basin of SE Oregon, NE California, and NC Nevada). P. l. pacificus Mearns, 1898 — SW USA (coastal plains of SW California to the USA-Mexico border). P. I. panamintinus Merriam, 1894 — SW USA (Great Basin of W Nevada and SE California). P. l. pimensis Huey, 1937 — SW USA (disjunct distribution in SC Arizona). P. l. salinensis Bole, 1937 — SW USA (restricted distribution in the Salinas Valley of SE California). P. l. tularensis Richardson, 1937 — SW USA (restricted distribution in the upper valley of the Kern River, SC California). P. l. venustus Huey, 1930 — NW Mexico (known only from the type locality of San Agustin, NC Baja California).
Distribution. NW Argentina, known only from the type locality in the Salar de Pipanaco, S Catamarca Province. in Octodontidae
Distribution. NW Argentina, known only from the type locality in the Salar de Pipanaco, S Catamarca Province.
Subspecies and Distribution. C.s.sclateriBroom,1907—fromBeaufortWestEalongKoueveldbergeandSneeubergetoGraaff-Reinet,WesternandEasternCapeprovinces,SSouthAfrica. C.s.guwillarmodiRoberts,1936—fromextremeEFreeStateandSWKwaZulu-NatalSthroughLesothotoCEasternCapeProvince,SouthAfrica. C.s.montanaRoberts,1924—knownonlyfromthetypelocalitynearWakkerstroom,MpumalangaProvince,ESouthAfrica. C. s. shortridgei Broom, 1950 — known only from the type locality in Sutherland, Northern Cape Province, W South Africa. in Chrysochloridae
Subspecies and Distribution. C.s.sclateriBroom,1907—fromBeaufortWestEalongKoueveldbergeandSneeubergetoGraaff-Reinet,WesternandEasternCapeprovinces,SSouthAfrica. C.s.guwillarmodiRoberts,1936—fromextremeEFreeStateandSWKwaZulu-NatalSthroughLesothotoCEasternCapeProvince,SouthAfrica. C.s.montanaRoberts,1924—knownonlyfromthetypelocalitynearWakkerstroom,MpumalangaProvince,ESouthAfrica. C. s. shortridgei Broom, 1950 — known only from the type locality in Sutherland, Northern Cape Province, W South Africa.
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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