Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
2,021
datasets available to search
ShareScore release 0.9.0
Dataset results
2,021 results for “valley”
FIGURES 1–8 in A new species of Pheraeus Godman, 1900 (Hesperiidae, Hesperiini, Moncina) restricted to Rio Doce Valley, Brazil
FIGURES 1–8. Pheraeus guandu sp. nov.: male: 1—dorsal view, 2—ventral view (holotype); female: 3—dorsal view, 4— ventral view (paratype). Pheraeus argynnis (Plötz, 1884): male: 5—dorsal view, 6—ventral view. Brazil, Catas Altas, Caraça, 1-5-II-1985, 1300-1500m, Mielke & Casagrande leg., DZ 40.755 (DZUP); female: 7—dorsal view, 8—ventral view. Brazil, Paraná, Tijucas do Sul, Rincão, 13-II-1969, 900m, Mielke & Laroca leg., DZ 40.775 (DZUP).
FIGURE 3 in Myoxanthus anancusiensis (Orchidaceae: Pleurothallidinae), a new species from the inter-Andean valley of Huancavelica, Peru
FIGURE 3. Isotype of Myoxanthus anancusiensis H.R.Quispe, R.D.Cuadros & F.H.Calderon. Specimen deposited in the HSP Herbarium. Photographed by Daniel Ramos.
FIGURE 2. Aenigmanu chococola. A in Taxonomic studies in Colombian Picramniaceae (Picramniales): new species of Aenigmanu, Nothotalisia and Picramnia from the Pacific and Magdalena Valley regions
FIGURE 2. Aenigmanu chococola. A. Flowering branchlet of pistillate plant. B. Stipules. C. Detail of leaves blade at very tip, abaxial view. D. Pistillate inflorescence. E. Pistillate flower beginning to develop fruit. (A–E from the holotype; illustration by Ana Cristina Pareja, HUA).
FIGURE 21 in Parasitoid wasps (Ichneumonoidea) collected from faba bean fields, Kharga Oasis, New Valley, Egypt, with new records and the description of a new species
FIGURE 21. Barichneumon bilunulatus (Gravenhorst, 1829) (♂): A, frontal view of head; B, dorsal view of mesosoma (part); C, fore and hind wings; D, propodeum and metasomal T1, T2, T3 (part).
FIGURE 9 in Parasitoid wasps (Ichneumonoidea) collected from faba bean fields, Kharga Oasis, New Valley, Egypt, with new records and the description of a new species
FIGURE 9. Centistes sp. (♂): A, lateral habitus; B, frontal habitus; C, fore wing; D, lateral view of head and mesosoma; E, dorsal view of head and mesosoma; F, propodeum and metasomal T1 & T2.
FIGURE 4. Potential distribution range for T in A new subspecies in the Turdus nudigenis complex (Aves: Turdidae) from the Cauca River valley of Colombia
FIGURE 4. Potential distribution range for T. grayi casius/incomptus (green area) and T. grayi suarezi (purple areas) in Colombia. T. g. casius/incomptus is predicted in the Caribbean lowlands of northern Colombia and in some areas of the Magdalena River valley, while T. g. suarezi is predicted mainly in the Cauca River valley and some lowland areas of the west slope of the West Andes and in the Magdalena River valley. The green and violet points are the records used for the niche modelling of T. g. casius/incomptus and T. g. suarezi, respectively.
FIGURE 5 in A new subspecies in the Turdus nudigenis complex (Aves: Turdidae) from the Cauca River valley of Colombia
FIGURE 5. Variation in songs in some subspecies of T. grayi and other taxa in the T. nudigenis complex. A. T. grayi casius (XC72519, R. P. O'Donnell), San José, Costa Rica. B. T. grayi casius (XC78591, W. Adsett), Altos de Torreón, Altos de Cerro Azul, Panama Province, Panama. C. T. grayi suarezi (XC404837, A. Angulo), Sabanalarga, dpto. Antioquia, Colombia. D. T. grayi suarezi (XC212493, M. Espejo), Hotel Tinamú Birding, vereda San Peregrino, Manizales, dpto. Caldas, Colombia. E. T. n. nudigenis (XC231876, P. Boesman), Casa María, Edo. Carabobo, Venezuela. F. T. n. nudigenis (XC181499, O. Ramos), PN San Esteban, Puerto Cabello, Edo. Carabobo, Venezuela.
FIGURE 7 in A new subspecies in the Turdus nudigenis complex (Aves: Turdidae) from the Cauca River valley of Colombia
FIGURE 7. Plumage variation among males of T. grayi suarezi (left), T. grayi casius (center) and T. n. nudigenis (right). Note the paler overall coloration of T. g. suarezi compared to the other taxa. Specimens exhibited: T. g. suarezi (ICN 39503; holotype); T. g. casius (ICN 35121), Granja Crocodylia, vereda La Florida, San Marcos, dpto. Sucre, Colombia; T. n. nudigenis (ICN 35988), finca La Marina, vereda El Manantial, San Martín, dpto. Meta, Colombia.
Subspecies and Distribution. H.a.aquaticusOgilby,1841—WAfricafromGuineaandSierraLeonetoGhana. H.a.bates:Lydekker,1906—Nigeria,Cameroon,andpresumablyneighboringcountries. H. a. cottoni Lydekker, 1906 — Republic of the Congo, DR Congo, and presumably Uganda. The Water Chevrotain reportedly has a disjunct distribution, occurring in coastal forests from West Africa and in the rainforests of Central Africa from Nigeria to DR Congo, marginally entering Uganda. It has been listed for the following countries in Central Africa: Angola (Cabinda), Cameroon, Central African Republic, DR Congo, Equatorial Guinea, Gabon, Nigeria, Republic of the Congo, and Uganda (Semliki Valley). A record from Angola's Lunda Norte Province, near the Cassai River,is the southernmost record of the species. The species' status in some countries remains unclear. It is apparently absent from the Republic of Benin and Togo (but the speciesis listed as probable in the Ot Basin in Togo); its supposed occurrence in Guinea Bissau and Senegal remains unsupported by evidence. The species was listed for Sierra Leone, although its presence had been called into question. Photographic evidence seems to clarify that the species occurs in Sierra Leone. In 1850, a specimen was recorded from Gambia, but the present status of the species is unclear. Local people report the species from the Boké Préfecture in NW Guinea, which might be the northernmost area from which the species has been recently reported. Extensive field and market surveys there and in the southern Guinea savanna belt did notfind evidence for the species' presence. in Tragulidae
Subspecies and Distribution. H.a.aquaticusOgilby,1841—WAfricafromGuineaandSierraLeonetoGhana. H.a.bates:Lydekker,1906—Nigeria,Cameroon,andpresumablyneighboringcountries. H. a. cottoni Lydekker, 1906 — Republic of the Congo, DR Congo, and presumably Uganda. The Water Chevrotain reportedly has a disjunct distribution, occurring in coastal forests from West Africa and in the rainforests of Central Africa from Nigeria to DR Congo, marginally entering Uganda. It has been listed for the following countries in Central Africa: Angola (Cabinda), Cameroon, Central African Republic, DR Congo, Equatorial Guinea, Gabon, Nigeria, Republic of the Congo, and Uganda (Semliki Valley). A record from Angola's Lunda Norte Province, near the Cassai River,is the southernmost record of the species. The species' status in some countries remains unclear. It is apparently absent from the Republic of Benin and Togo (but the speciesis listed as probable in the Ot Basin in Togo); its supposed occurrence in Guinea Bissau and Senegal remains unsupported by evidence. The species was listed for Sierra Leone, although its presence had been called into question. Photographic evidence seems to clarify that the species occurs in Sierra Leone. In 1850, a specimen was recorded from Gambia, but the present status of the species is unclear. Local people report the species from the Boké Préfecture in NW Guinea, which might be the northernmost area from which the species has been recently reported. Extensive field and market surveys there and in the southern Guinea savanna belt did notfind evidence for the species' presence.
Distribution. NW Colombia in the Pacific lowlands (E to the Sinu Valley, S towards the Ecuadorian border, and N into Cordoba Department, perhaps as far as Valdivia where it would overlap with the Gray-legged Night Monkey, A. griseimembra), and most of Panama (along the Pacific coast W to the Rio San Pedro in Veraguas and on the Atlantic side W as far as the Rio Changuinola in Bocas del Toro); it is absent from SW Panama (Chiriqui), and its occurrence in SE Costa Rica is uncertain. in Aotidae
Distribution. NW Colombia in the Pacific lowlands (E to the Sinu Valley, S towards the Ecuadorian border, and N into Cordoba Department, perhaps as far as Valdivia where it would overlap with the Gray-legged Night Monkey, A. griseimembra), and most of Panama (along the Pacific coast W to the Rio San Pedro in Veraguas and on the Atlantic side W as far as the Rio Changuinola in Bocas del Toro); it is absent from SW Panama (Chiriqui), and its occurrence in SE Costa Rica is uncertain.
Subspecies and Distribution. A. g. guariba Humboldt, 1812 — Brazilian Atlantic Forest from the Rio Sao Francisco (although the Rio Paraguacu is the northernmost known locality) to the Rio Doce; however, based on his studies of morphology and pelage color patterns Gregorin in 2006 indicated that it extends from the Rio Paraguacu in Bahia State, S along the coast across the lower Rio Jequitinhonha extending inland somewhat into Minas Gerais State, S through the Rio Doce valley as far the Rio Paraiba do Sul Basin in Rio de Janeiro. A. g. clamitans Cabrera, 1940 — Brazilian Atlantic Forest S of Rio Doce (but Gregorin has recently identified howlers of the upper Rio Doce, Rio Matip6 and Caratinga, and the middle and upper Rio Jequitinhonha as marking the N limits of this subspecies) through the S of Espirito Santo to Rio de Janeiro, Sao Paulo, Parana, Santa Catarina, and Rio Grande do Sulstates (S limit is Rio Camaqua Basin in Rio Grande do Sul, 31° 10" S, where the Atlantic Forest gives way to the Pampas grasslands), and inland in the forested E of Minas Gerais ("Zona da Mata") and the Brazilian Highlands; also in NE Argentina (E of the Mts in Misiones Province to ¢.28° S). in Atelidae
Subspecies and Distribution. A. g. guariba Humboldt, 1812 — Brazilian Atlantic Forest from the Rio Sao Francisco (although the Rio Paraguacu is the northernmost known locality) to the Rio Doce; however, based on his studies of morphology and pelage color patterns Gregorin in 2006 indicated that it extends from the Rio Paraguacu in Bahia State, S along the coast across the lower Rio Jequitinhonha extending inland somewhat into Minas Gerais State, S through the Rio Doce valley as far the Rio Paraiba do Sul Basin in Rio de Janeiro. A. g. clamitans Cabrera, 1940 — Brazilian Atlantic Forest S of Rio Doce (but Gregorin has recently identified howlers of the upper Rio Doce, Rio Matip6 and Caratinga, and the middle and upper Rio Jequitinhonha as marking the N limits of this subspecies) through the S of Espirito Santo to Rio de Janeiro, Sao Paulo, Parana, Santa Catarina, and Rio Grande do Sulstates (S limit is Rio Camaqua Basin in Rio Grande do Sul, 31° 10" S, where the Atlantic Forest gives way to the Pampas grasslands), and inland in the forested E of Minas Gerais ("Zona da Mata") and the Brazilian Highlands; also in NE Argentina (E of the Mts in Misiones Province to ¢.28° S).
Distribution. Along the Andes of Colombia, Ecuador, and Peru, including intermontane valleys and adjacent Amazon lowlands. It might occur in N Bolivia and W Brazillan Amazonia. in Vespertilionidae
Distribution. Along the Andes of Colombia, Ecuador, and Peru, including intermontane valleys and adjacent Amazon lowlands. It might occur in N Bolivia and W Brazillan Amazonia.
Distribution. From Senegal and Gambia to N Ethiopia and Eritrea, and S to Zambia;; isolated populations exist in S Gabon, W Republic of the Congo, and Angola. The Rift Valley in C Kenya and C Tanzania forms the E distributionallimit; distribution to the S is restricted by the Muchinga escarpment in Zambia. in Bovidae
Distribution. From Senegal and Gambia to N Ethiopia and Eritrea, and S to Zambia;; isolated populations exist in S Gabon, W Republic of the Congo, and Angola. The Rift Valley in C Kenya and C Tanzania forms the E distributionallimit; distribution to the S is restricted by the Muchinga escarpment in Zambia.
Distribution. From Lake Chad to E Sudan and possibly just into Ethiopia, SE to the borders of the East African Rift Valley, S to the Uasin Gishu Plateau in Kenya and to Ankole in Uganda. in Bovidae
Distribution. From Lake Chad to E Sudan and possibly just into Ethiopia, SE to the borders of the East African Rift Valley, S to the Uasin Gishu Plateau in Kenya and to Ankole in Uganda.
Subspecies and Distribution. S.t.telumLichtenstein,1823—Kazakhstan(Aktobe,Atyrau,WEastKazakhstan,Karaganda,SKostanay,NKyzylorda,andWestKazakhstanregions). S.t.amankaragaiSelevin,1934—NKazakhstan(NKostanayRegion). S.t.birulaeVinogradov,1937—EKazakhstan(ELakeZaysanBasin)andNWChina(NWXinjiang). S.t.falzferiniBrauner,1913—SUkraine(leftbankoflowerDnieperRiverValleyinMikolaivandKhersonregions). S.t.nastjukoviShenbrot,1991—SKazakhstan(Mangystau,SKyzylorda,Jambyl,andSAlmatyregions),NWUzbekistan(Karakalpakstan),andW&NTurkmenistan(BalkhanandDasoguzregions). S. t. turovi Heptner, 1934 — S European Russia (middle Don Valley in Volgograd and Rostov regions E & S to the right bank of Volga in Astrakhan, Kalmykia, N S.t., and Dagestan). in Dipodidae
Subspecies and Distribution. S.t.telumLichtenstein,1823—Kazakhstan(Aktobe,Atyrau,WEastKazakhstan,Karaganda,SKostanay,NKyzylorda,andWestKazakhstanregions). S.t.amankaragaiSelevin,1934—NKazakhstan(NKostanayRegion). S.t.birulaeVinogradov,1937—EKazakhstan(ELakeZaysanBasin)andNWChina(NWXinjiang). S.t.falzferiniBrauner,1913—SUkraine(leftbankoflowerDnieperRiverValleyinMikolaivandKhersonregions). S.t.nastjukoviShenbrot,1991—SKazakhstan(Mangystau,SKyzylorda,Jambyl,andSAlmatyregions),NWUzbekistan(Karakalpakstan),andW&NTurkmenistan(BalkhanandDasoguzregions). S. t. turovi Heptner, 1934 — S European Russia (middle Don Valley in Volgograd and Rostov regions E & S to the right bank of Volga in Astrakhan, Kalmykia, N S.t., and Dagestan).
Subspecies and Distribution. D.a.agilisGambel,1848—SWUSA(LosAngelesBasinandfoothillsofSanGabrielandSanBernardinoMtsofSWCalifornia). D. a. perplexus Merriam, 1907 — SW USA (S Sierra Nevada, Tehachapi, and San Gabriel Mts, N San Fernando Valley of SW California). in Heteromyidae
Subspecies and Distribution. D.a.agilisGambel,1848—SWUSA(LosAngelesBasinandfoothillsofSanGabrielandSanBernardinoMtsofSWCalifornia). D. a. perplexus Merriam, 1907 — SW USA (S Sierra Nevada, Tehachapi, and San Gabriel Mts, N San Fernando Valley of SW California).
Subspecies and Distribution. D.c.californicusMerriam,1890—WUSA(NoftheSacramento-SanJoaquinEstuarysystemintheCoastMtsofNCaliforniatoSOregonandontheModocPlateautotheCalifornia—Nevadaborder). D.c.eximiusGrinnell,1919—WUSA(restrictedtovicinityofMarysvilleButtesinNCalifornia),butmaybeextinct. D. c. saxatilis Grinnell & Linsdale, 1929 — W USA (foothills on E edge of the Sacramento Valley, N California). in Heteromyidae
Subspecies and Distribution. D.c.californicusMerriam,1890—WUSA(NoftheSacramento-SanJoaquinEstuarysystemintheCoastMtsofNCaliforniatoSOregonandontheModocPlateautotheCalifornia—Nevadaborder). D.c.eximiusGrinnell,1919—WUSA(restrictedtovicinityofMarysvilleButtesinNCalifornia),butmaybeextinct. D. c. saxatilis Grinnell & Linsdale, 1929 — W USA (foothills on E edge of the Sacramento Valley, N California).
Subspecies and Distribution. L. t. timidus Linnaeus, 1758 — Scandinavia S to 59° N, N Russia (S to 57° N to 58° N) to E of Ural Mts, Estonia, perhaps Poland, and Altai and Beita Mts in N Xinjiang (China); from Sweden extending in hybrid zones with the subspecies sylvaticus to S coast of Norway and W Latvia. L. t. abet Kuroda, 1938 — Kurile Is (Russia). L. t. ainu Barrett-Hamilton, 1900 — Hokkaido (Japan). L. t. begitschevi Koljuschev, 1936 — Taimyr Peninsula (Russia). L. t. gichiganus J. A. Allen, 1903 — C Yakutia, Kamchatka and Okhotsk Sea coast (Russia). L. t. hibernicus Bell, 1837 — Ireland. L. t. kolymensis Ognev, 1922 — NE Siberia (Russia). L. t. kozhevnikovi Ognev, 1929 — C Russia from 57° to 58°N, whereit intergrades with the nomonotypical timidus S to 53° N. The W boundary is unclear. L. t. lugubris Kastschenko, 1899 — Siberian Altai Mts (Russia). L. t. mordeni Goodwin, 1933 — Russian Far East (Ussuri Valley and lower and middle Amur River) and Heilongjiang (China). L. t. ori Kuroda, 1928 — Sakhalin (Russia). L. t. scoticus Hilzheimer, 1906 — Scotland. L. t. sibiricorumJohansen, 1923 — W & SW Siberia (Russia), N Kazakhstan, and Tacheng Mts in N Xinjiang (China). L. t. sylvaticus Nilsson, 1831 —S Sweden, extending in hybrid zones with nominotypical timidus to S coast of Norway and W Latvia. L. t. transbaikalicus Ognev, 1929 — Trans-Baikal region in E Siberia (Russia) and E Inner Mongolia (= Nei Mongol, China). L. t. varronis Miller, 1901 — at high altitudes in the Alps, C Europe. in Leporidae
Subspecies and Distribution. L. t. timidus Linnaeus, 1758 — Scandinavia S to 59° N, N Russia (S to 57° N to 58° N) to E of Ural Mts, Estonia, perhaps Poland, and Altai and Beita Mts in N Xinjiang (China); from Sweden extending in hybrid zones with the subspecies sylvaticus to S coast of Norway and W Latvia. L. t. abet Kuroda, 1938 — Kurile Is (Russia). L. t. ainu Barrett-Hamilton, 1900 — Hokkaido (Japan). L. t. begitschevi Koljuschev, 1936 — Taimyr Peninsula (Russia). L. t. gichiganus J. A. Allen, 1903 — C Yakutia, Kamchatka and Okhotsk Sea coast (Russia). L. t. hibernicus Bell, 1837 — Ireland. L. t. kolymensis Ognev, 1922 — NE Siberia (Russia). L. t. kozhevnikovi Ognev, 1929 — C Russia from 57° to 58°N, whereit intergrades with the nomonotypical timidus S to 53° N. The W boundary is unclear. L. t. lugubris Kastschenko, 1899 — Siberian Altai Mts (Russia). L. t. mordeni Goodwin, 1933 — Russian Far East (Ussuri Valley and lower and middle Amur River) and Heilongjiang (China). L. t. ori Kuroda, 1928 — Sakhalin (Russia). L. t. scoticus Hilzheimer, 1906 — Scotland. L. t. sibiricorumJohansen, 1923 — W & SW Siberia (Russia), N Kazakhstan, and Tacheng Mts in N Xinjiang (China). L. t. sylvaticus Nilsson, 1831 —S Sweden, extending in hybrid zones with nominotypical timidus to S coast of Norway and W Latvia. L. t. transbaikalicus Ognev, 1929 — Trans-Baikal region in E Siberia (Russia) and E Inner Mongolia (= Nei Mongol, China). L. t. varronis Miller, 1901 — at high altitudes in the Alps, C Europe.
Distribution. NE India, marginally in the states of Arunachal Pradesh (Lohit and Lower Dibang Valley districts) and Assam (Tinsukia District), E Myanmar (E of the Chindwin River), and S China in W Yunnan Province. in Hylobatidae
Distribution. NE India, marginally in the states of Arunachal Pradesh (Lohit and Lower Dibang Valley districts) and Assam (Tinsukia District), E Myanmar (E of the Chindwin River), and S China in W Yunnan Province.
Sacred Valley, Peru, 2017
<u>Source</u>: Flickr <br><u>4DCity URL</u>: <a href="https://4dcity.org/imgupload/1665336860.8564.jpg">https://4dcity.org/imgupload/1665336860.8564.jpg</a> <br><u>Original Image URL</u>: <a href="https://live.staticflickr.com/642/32197930115_1beeeee14e_m.jpg">https://live.staticflickr.com/642/32197930115_1beeeee14e_m.jpg</a> <br><br><u>Image-Metadata:</u><br>Filename: 1665336860.8564.jpg<br>Image Dimensions: 180x240<br>Megapixels: 0.04 MP<br>Filesize: 11.75 KB<br><br>ExifOffset: 38
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.