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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.
FIGURE 8. Type specimens and label data. A in Korean species of the Atheta Thomson subgenus Dimetrota Mulsant & Rey (Coleoptera: Staphylinidae: Aleocharinae) with a description of new species
FIGURE 8. Type specimens and label data. A: lectotype of Atheta (Dimetrota) altaica; B: syntype of A. (D.) sublaevana [= A. (D.) atramentaria]; C: holotype of A. (D.) sulputrida [= A. (D.) atramentaria]; D: lectotype of A. (D.) furtiva; E: holotype of A. (D.) machonryongica; F: holotype of A. (D.) photaechonica; G: lectotype of A. (D.) subsericans; H: syntype of A. (Dimetrota) weisei; I: holotype of A. (D.) chagangensis = A. (Badura) tokiokai.
FIGURE. Phylogenetic tree derived from Bayesian analysis, based on nrLSU data. Posterior probability (PP> 0.95) values from the Bayesian analysis are added at the nodes. The scale bar represents the number of nucleotide changes per site. (T) indicates the type specimen for this species. The new species are in bold. in Four new species of Entoloma (Entolomataceae, Agaricomycetes) subgenera Cyanula and Claudopus from Vietnam and their phylogenetic position
FIGURE. Phylogenetic tree derived from Bayesian analysis, based on nrLSU data. Posterior probability (PP> 0.95) values from the Bayesian analysis are added at the nodes. The scale bar represents the number of nucleotide changes per site. (T) indicates the type specimen for this species. The new species are in bold.
Distribution. Known from only two isolated localities (Ingwavuma and Ubombo) on E slopes of Lebombo Mts, KwaZulu-Natal Province, E South Africa; owl pellet remains from Weenen, ¢.250 km SW of type locality, appear to represent this species, suggesting that it is more widespread than currently recognized. Possibly extends into SE Swaziland along the Lebombo Mts. in Chrysochloridae
Distribution. Known from only two isolated localities (Ingwavuma and Ubombo) on E slopes of Lebombo Mts, KwaZulu-Natal Province, E South Africa; owl pellet remains from Weenen, ¢.250 km SW of type locality, appear to represent this species, suggesting that it is more widespread than currently recognized. Possibly extends into SE Swaziland along the Lebombo Mts.
Distribution. NW Madagascar, confined to the Lokobe region on Nosy Be. This may or may not be the species that occurred on the island of Nosy Komba as well, but in any case sportive lemurs have not been observed there for several years; in 2007, D. Zinner and coworkers found that some specimens from the mainland had identical mtDNA to that of the type specimen of the Nosy Be Sportive Lemur. in Lepilemuridae
Distribution. NW Madagascar, confined to the Lokobe region on Nosy Be. This may or may not be the species that occurred on the island of Nosy Komba as well, but in any case sportive lemurs have not been observed there for several years; in 2007, D. Zinner and coworkers found that some specimens from the mainland had identical mtDNA to that of the type specimen of the Nosy Be Sportive Lemur.
Distribution. NW Madagascar; the range is still incompletely known, but it is believed to be restricted to the Ankarafantsika region; the type specimen was collected adjacent to Lac Ravelobe in Ankarafantsika National Park, and the species is also known to occur in the Mariarano Classified Forest, just N of Mahajanga. in Cheirogaleidae
Distribution. NW Madagascar; the range is still incompletely known, but it is believed to be restricted to the Ankarafantsika region; the type specimen was collected adjacent to Lac Ravelobe in Ankarafantsika National Park, and the species is also known to occur in the Mariarano Classified Forest, just N of Mahajanga.
FIGURE 1. Type locality marked with a in Description of a new species of Liropus (Crustacea, Amphipoda) from Puerto Vallarta, Pacific coast of Mexico
FIGURE 1. Type locality marked with a filled circle in Los Arcos National Marine Park, near the city of Puerto Vallarta, Jalisco, Mexico.
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.
FIGURES 22–26. 22 in The primary types of Bisaltes (Bisaltes) Thomson of the Museu de Zoologia Universidade de São Paulo, with notes and synonymies regarding other species of this subgenus and Bisaltes (Craspedocerus) Aurivillius (Coleoptera, Cerambycidae Lamiinae)
FIGURES 22–26. 22) Bisaltes strandi Breuning, 1940, holotype, by Jesus Santiago Moure. 23) Bisaltes fuscoapicalis Breuning, 1950, holotype female, by Jesus Santiago Moure. 24) Bisaltes subreticulatus Aurivillius, 1920, holotype, by Jesus Santiago Moure. 25) Bisaltes spegazzinii Bruch, 1911, syntype, from the original description. 26) Bisaltes venezuelensis Breuning, 1943, holotype, by Jesus Santiago Moure.
FIGURES 1–6 in The primary types of Bisaltes (Bisaltes) Thomson of the Museu de Zoologia Universidade de São Paulo, with notes and synonymies regarding other species of this subgenus and Bisaltes (Craspedocerus) Aurivillius (Coleoptera, Cerambycidae Lamiinae)
FIGURES 1–6. Bisaltes (Bisaltes) pulvereus (Bates, 1866). 1–4) B. (B.) petilus Galileo & Martins, 2009, holotype female: 1) Dorsal habitus; 2) Ventral habitus; 3) Lateral habitus; 4) Labels. 5) Esthlogena pulverea Bates, 1866, holotype, by Jesus Santiago Moure. 6) B. (B.) posticalis Thomson, 1868, holotype, by Jesus Santiago Moure.
FIGURES 15–21. 15–18 in The primary types of Bisaltes (Bisaltes) Thomson of the Museu de Zoologia Universidade de São Paulo, with notes and synonymies regarding other species of this subgenus and Bisaltes (Craspedocerus) Aurivillius (Coleoptera, Cerambycidae Lamiinae)
FIGURES 15–21. 15–18) Bisaltes (Bisaltes) unicolor Galileo & Martins, 2003, holotype male: 15) Dorsal habitus; 16) Ventral habitus; 17) Lateral habitus; 18) Labels. 19–21) Bisaltes fuscomarmoratus, Breuning, 1966, holotype female: 19) Labels; 20) Dorsal habitus; 21) Lateral habitus. Figures 19–21 by Julien Lalanne.
FIGURES 27–35. 27 in The primary types of Bisaltes (Bisaltes) Thomson of the Museu de Zoologia Universidade de São Paulo, with notes and synonymies regarding other species of this subgenus and Bisaltes (Craspedocerus) Aurivillius (Coleoptera, Cerambycidae Lamiinae)
FIGURES 27–35. 27) Bisaltes buquetii Thomson, 1868, holotype female. 28) Bisaltes triangularis Breuning, 1940, holotype. 29) Bisaltes flaviceps Breuning, 1940, holotype. 30–31) Bisaltes fuscodiscalis Breuning, 1943, holotype female: 30) Dorsal habitus; 31) Basal antennomeres. 32) Bisaltes (Craspedocerus) ptericoptoides Breuning, 1942, holotype 33) Bisaltes pictus Breuning, 1940, holotype. 34) Craspedocerus poecilus Aurivillius, 1900, syntype male. 35) Bisaltes columbianus Breuning, 1971, holotype. Figures 27–34 by Jesus Santiago Moure; figure 35 by John Chemsak.
FIGURES 7–14. 7–10 in The primary types of Bisaltes (Bisaltes) Thomson of the Museu de Zoologia Universidade de São Paulo, with notes and synonymies regarding other species of this subgenus and Bisaltes (Craspedocerus) Aurivillius (Coleoptera, Cerambycidae Lamiinae)
FIGURES 7–14. 7–10) Bisaltes (Bisaltes) picticornis Galileo & Martins, 2003, holotype male: 7) Dorsal habitus; 8) Ventral habitus; 9) Lateral habitus; 10) Labels. 11–14) Bisaltes (Bisaltes) taua Galileo & Martins, 2003, holotype female: 11a-c) Labels; 12) Dorsal habitus; 13) Ventral habitus; 14) Lateral habitus.
FIGURE 9. Type locality for Faxonius elix n in Description of a new species of crayfish in the genus Faxonius (Decapoda: Cambaridae) from the Lower Ohio River Drainage, with evidence of glacial influence on the distribution of some crayfish species throughout the Ohio River basin
FIGURE 9. Type locality for Faxonius elix n. sp., Fern Creek at Feganbush Lane (Kentucky Highway 864) crossing, Jefferson County, Kentucky (38.160374o N, -85.639214o W. Photograph taken on November 19, 2018.
Distribution. Uncertain, but the type locality is generally accepted to be Mt Kilimanjaro, NE Tanzania; there are further reports of this species throughout W & E Africa (including some recent ones from Uganda), but they cannot be confirmed since most of the specimens have been wrongly attributed. in Soricidae
Distribution. Uncertain, but the type locality is generally accepted to be Mt Kilimanjaro, NE Tanzania; there are further reports of this species throughout W & E Africa (including some recent ones from Uganda), but they cannot be confirmed since most of the specimens have been wrongly attributed.
Subspecies and Distribution. C.d.draculaThomas,1912—C&SCChina(Sichuan,Yunnan,Chongqing,Guizhou,andGuangxi),NLaos,andNVietnam. C. d. mansumensis Carter, 1942 — known only from the type locality in N Myanmar; range limits unclear because the species has been recognized as a synonym for a long time, probably N Myanmar. in Soricidae
Subspecies and Distribution. C.d.draculaThomas,1912—C&SCChina(Sichuan,Yunnan,Chongqing,Guizhou,andGuangxi),NLaos,andNVietnam. C. d. mansumensis Carter, 1942 — known only from the type locality in N Myanmar; range limits unclear because the species has been recognized as a synonym for a long time, probably N Myanmar.
Distribution. India, the species' range extends 1900 km W to E, and includes all populations with the northern-type tail carriage between the Tapti River in Gujarat State and Krishna River in Andhra Pradesh State to the foothills of the Himalaya. Introduced into SW Bangladesh, where the population may have arisen from descendents of a pair introduced by Hindu pilgrims on the banks of the Jalangi River. in Cercopithecidae
Distribution. India, the species' range extends 1900 km W to E, and includes all populations with the northern-type tail carriage between the Tapti River in Gujarat State and Krishna River in Andhra Pradesh State to the foothills of the Himalaya. Introduced into SW Bangladesh, where the population may have arisen from descendents of a pair introduced by Hindu pilgrims on the banks of the Jalangi River.
Lophuromys margarettae was initially de- scribed as a subspecies of L. aquilus and later synonymized under L. flavopunctatus. It was elevated to a distinct species based on analyses of external and skull measurements and mtDNA of specimens from the type locality. Monotypic. Distribution. Highlands of W Uganda and Kenya. in Muridae
Lophuromys margarettae was initially de- scribed as a subspecies of L. aquilus and later synonymized under L. flavopunctatus. It was elevated to a distinct species based on analyses of external and skull measurements and mtDNA of specimens from the type locality. Monotypic. Distribution. Highlands of W Uganda and Kenya.
Lophuromys stanley: is member of the L. flavopunctatus species complex and was named during partial revision of the L. aguilus species complex. It is characterized by craniometric and genetic character-istics; its skull proportions are similar to L. laticeps, and molecularly, it is similar to L. margarettae and L. zena (cytochrome-b). Lophuromys stanleyi is one of four endemic species in the Rwenzori Mountains diversity hotspot. Monotypic. Distribution. Rwenzori Mts, E DR Congo and SW Uganda. Descriptive notes. Head-body 113-126 mm, tail 40-80 mm, ear 16-19 mm, hindfoot 22-24 mm; weight 36-55 g. The Rwenzori Brush-furred Rat has a speckled pelage similar to other speciesin the L. flavopunctatus species complex. Tail is short, 50-60% of head-body length. Habitat. Poorly known, but type specimen was collected at an elevation of 3700 m. Food and Feeding. No information. Breeding. No information. Activity patterns. No information. in Muridae
Lophuromys stanley: is member of the L. flavopunctatus species complex and was named during partial revision of the L. aguilus species complex. It is characterized by craniometric and genetic character-istics; its skull proportions are similar to L. laticeps, and molecularly, it is similar to L. margarettae and L. zena (cytochrome-b). Lophuromys stanleyi is one of four endemic species in the Rwenzori Mountains diversity hotspot. Monotypic. Distribution. Rwenzori Mts, E DR Congo and SW Uganda. Descriptive notes. Head-body 113-126 mm, tail 40-80 mm, ear 16-19 mm, hindfoot 22-24 mm; weight 36-55 g. The Rwenzori Brush-furred Rat has a speckled pelage similar to other speciesin the L. flavopunctatus species complex. Tail is short, 50-60% of head-body length. Habitat. Poorly known, but type specimen was collected at an elevation of 3700 m. Food and Feeding. No information. Breeding. No information. Activity patterns. No information.
FIGURES 37–51 in Types of species of Ectinogonia (Coleoptera: Buprestidae) described by Antonio Cobos Sánchez deposited in the Museo Nacional de Ciencias Naturales, Madrid
FIGURES 37–51. Type specimens of Ectinogonia spp. 37–39) Syntype of Ectinogonia chalyboeiventris wagenknechti Cobos, 1954: Dorsal and lateral view, and labels. 40–42) ¿Syntype? of Ectinogonia minor Olave, 1936: Dorsal and lateral view, and labels. 43–48) Syntype of Ectinogonia penai Cobos, 1954: Dorsal and lateral view, and labels. Scale bars: 5 mm. 49–51) Nontype specimen of Ectinogonia buqueti speciosa var. obscuripennis Cobos, 1954: Dorsal and lateral view, and labels. Scale bars: 1 mm.
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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)
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DANDI Archive for NWB datasets
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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.