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33 results for “lowland areas”
Text-fig. 5. Profiles of the Konin region with the backgroundstratigraphy of the upper part of the Neogene in the Polish Lowlands. in Micropalaeontological Taphocoenoses Of The Miocene Poznań Formation (Konin Area, Central Poland)
Text-fig. 5. Profiles of the Konin region with the backgroundstratigraphy of the upper part of the Neogene in the Polish Lowlands.
Fig. 6 in Areas of endemism in Thailand: has historical partitioning between seasonally dry lowland and aseasonal moist mountain forests shaped biodiversity in Southeast Asia?
Fig. 6. Relationship between elevation and geographical range of Hybos spp. in Thailand. The number of 1° grids in which a species was recorded is plotted against the median elevation of all records. Line fitted by linear regression in PAST (r2=0.1026).
Fig. 5 in Areas of endemism in Thailand: has historical partitioning between seasonally dry lowland and aseasonal moist mountain forests shaped biodiversity in Southeast Asia?
Fig. 5. EZPAE down-weighted against homoplasy, using altitudinally zoned mountain ranges as OGU, 'characters' made additive. Strict consensus tree of two equally parsimonious trees (CI = 0.716, RI = 0.534) produced by maximum parsimony analysis with weighted 'characters' and TBR branch swapping in TNT. Symmetrical resampling support is given under the nodes. Alphabetic codes of termini correspond with mountain ranges as abbreviated in Fig. 3; the suffixes 'low' & 'high' refer to low (<1,250m) and high (>1,250m) elevation sample data.
Fig. 4 in Areas of endemism in Thailand: has historical partitioning between seasonally dry lowland and aseasonal moist mountain forests shaped biodiversity in Southeast Asia?
Fig. 4. EZPAE down-weighted against homoplasy, using altitudinally zoned mountain ranges as OGU, 'characters' made non-additive. Strict consensus tree of four equally parsimonious trees (CI = 0.674, 0.580) produced by maximum parsimony analysis with weighted 'characters' and TBR branch swapping in TNT. Symmetrical resampling support is given under the nodes. Alphabetic codes of termini correspond with mountain ranges as abbreviated in Fig. 3; the suffixes 'low' & 'high' refer to low (<1,250m) and high (>1,250m) sample data.
Fig. 2. PAE using 1 in Areas of endemism in Thailand: has historical partitioning between seasonally dry lowland and aseasonal moist mountain forests shaped biodiversity in Southeast Asia?
Fig. 2. PAE using 1° grids as OGU. Strict consensus tree of 760 equally parsimonious trees (CI = 0.501, RI = 0.557) produced by maximum parsimony analysis with unweighted 'characters' and TBR branch swapping in TNT. Symmetrical resampling support is given under the nodes (see Fig 1A for explanation of alphabetic codes).
Fig. 3 in Areas of endemism in Thailand: has historical partitioning between seasonally dry lowland and aseasonal moist mountain forests shaped biodiversity in Southeast Asia?
Fig. 3. PAE using mountain ranges as OGU. Strict consensus tree of nine equally parsimonious trees (CI = 0.745, RI = 0.722) produced by maximum parsimony analysis with weighted 'characters' and implicit enumeration in TNT. Symmetrical resampling support is given under the nodes. Abbreviations. – CM, Cardamom Mountains; DK, Dong Paya Yen – Khao Yai Forest Complex; DL, Daen Lao Range; LP, Luang Prabang Range; NST, Nakhon Si Thammarat Range; PM, Petchabun Mountains; PR, Phuket Range; PPR, Phu Pan Range; TH, Tenasserim Hills; TT, Thanon Thongchai Range. Grid-B and Grid-L refer to 1° grids (B and L in Fig. 1A) that were not assigned to any mountain range.
Fig. 1 in Areas of endemism in Thailand: has historical partitioning between seasonally dry lowland and aseasonal moist mountain forests shaped biodiversity in Southeast Asia?
Fig. 1. Maps of Thailand showing: A, Grid of 1° of latitude and longitude denoted by single-letters A–W. Mountain ranges are indicated by two- or three letter codes (CD, DK, DL, LP, NST, PM, PPR, PR, TH & TT) and the grids that comprise each range are colour-coded. Grids B and L were not assigned to any mountain range; B, Species richness (number of species) of Hybos present in 1° grids; C, reciprocal weighted endemicity of Hybos spp. calculated for 1° grids.
FIG. 8. Amazon and Paraguay Lowlands. A. Yellow area delimits the distribution pattern. B in The Fishes Of The Amazon: Distribution And Biogeographical Patterns, With A Comprehensive List Of Species
FIG. 8. Amazon and Paraguay Lowlands. A. Yellow area delimits the distribution pattern. B. Epapterus dispilurus (data from Vari and Ferraris, 1998). C. Hemigrammus lunatus (data from Ota et al., 2014). D. Mesonauta festivus (data from Kullander and Silvergrip, 1991, and Schindler, 2005).
FIG. 9. Amazon-only Lowland. A. Yellow area delimits the distribution pattern. B in The Fishes Of The Amazon: Distribution And Biogeographical Patterns, With A Comprehensive List Of Species
FIG. 9. Amazon-only Lowland. A. Yellow area delimits the distribution pattern. B. Adontosternarchus balaenops (data from Mago-Leccia et al., 1985). C. Cetopsis candiru (data from Vari et al., 2005). D. Curimatella meyeri (data from Vari, 1992a).
FIG. 7. Amazon and Orinoco Lowlands. A. Yellow area delimits the distribution pattern. B in The Fishes Of The Amazon: Distribution And Biogeographical Patterns, With A Comprehensive List Of Species
FIG. 7. Amazon and Orinoco Lowlands. A. Yellow area delimits the distribution pattern. B. Moenkhausia lepidura (data from Marinho and Langeani, 2016). C. Potamorhina altamazonica (data from Vari, 1984). D. Vandellia cirrhosa (M.P., unpublished data).
High-performing plastic clones best explain the spread of yellow monkeyflower from lowland to higher elevation areas in New Zealand
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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. Lowlands of EC Ethiopia (Awash area) and NW Somalia. The exact southern limit of the Northern Lesser Kudu''s distribution in eastern Ethiopia requires additional research. in Bovidae
Distribution. Lowlands of EC Ethiopia (Awash area) and NW Somalia. The exact southern limit of the Northern Lesser Kudu''s distribution in eastern Ethiopia requires additional research.
Distribution. Two disjunct areas across the lowland rainforest belt of W Africa (Guinea, Sierra Leone, Liberia, Ivory Coast, Ghana, Togo & Benin) and C Africa through the Congo Basin (Cameroon, Gabon, Republic of the Congo, DR Congo, Central African Republic & extreme SW Sudan), and five very small disjunct populations in mountainous areas in C Kenya. in Bovidae
Distribution. Two disjunct areas across the lowland rainforest belt of W Africa (Guinea, Sierra Leone, Liberia, Ivory Coast, Ghana, Togo & Benin) and C Africa through the Congo Basin (Cameroon, Gabon, Republic of the Congo, DR Congo, Central African Republic & extreme SW Sudan), and five very small disjunct populations in mountainous areas in C Kenya.
Distribution. NE Pakistan, lowland areas of S Nepal, and Peninsular India. Introduced into Italy near Rome (extirpated during World War II), South Africa, S USA (Texas), and N Mexico (Coahuila, Nuevo Leon, Sonora, Tamaulipas & Veracruz). in Bovidae
Distribution. NE Pakistan, lowland areas of S Nepal, and Peninsular India. Introduced into Italy near Rome (extirpated during World War II), South Africa, S USA (Texas), and N Mexico (Coahuila, Nuevo Leon, Sonora, Tamaulipas & Veracruz).
Subspecies and Distribution. A. p. palliata Gray, 1849 — NE Guatemala (Rio Motagua, and possibly along the coast a short distance to Cabo de Tres Puntas, where it meets the distribution of the Central American Black Howler, A. pigra), E to E Costa Rica or W Panama; it is not found in El Salvador, although it may have occurred there in the past. A. p. aequatorialis Festa, 1903 — from the S distributional limits of the nominate subspecies palliata (either in E Costa Rica or W Panama) through the Serrania del Darién into W Colombia (N through basins of the rios Sint and Atrato to the Caribbean coast, and S through the Serrania del Baudo and the foothills, lowlands, and lower montane areas W of the Andes to the Pacific coast), W Ecuador, and NW Peru (extreme N of Tumbes Department). A. p. coibensis Thomas, 1902 — SW Panama (Coiba and Jicaron Is). A. p. mexicana Merriam, 1902 — S & SE Mexico (states of Veracruz, Tabasco, Campeche, Oaxaca, and N Chiapas) and Guatemala, in a swathe skirting the S of the distribution of the Central American Black Howler. A. p. trabeata Lawrence, 1933 — SW Panama (Azuero Peninsula). in Atelidae
Subspecies and Distribution. A. p. palliata Gray, 1849 — NE Guatemala (Rio Motagua, and possibly along the coast a short distance to Cabo de Tres Puntas, where it meets the distribution of the Central American Black Howler, A. pigra), E to E Costa Rica or W Panama; it is not found in El Salvador, although it may have occurred there in the past. A. p. aequatorialis Festa, 1903 — from the S distributional limits of the nominate subspecies palliata (either in E Costa Rica or W Panama) through the Serrania del Darién into W Colombia (N through basins of the rios Sint and Atrato to the Caribbean coast, and S through the Serrania del Baudo and the foothills, lowlands, and lower montane areas W of the Andes to the Pacific coast), W Ecuador, and NW Peru (extreme N of Tumbes Department). A. p. coibensis Thomas, 1902 — SW Panama (Coiba and Jicaron Is). A. p. mexicana Merriam, 1902 — S & SE Mexico (states of Veracruz, Tabasco, Campeche, Oaxaca, and N Chiapas) and Guatemala, in a swathe skirting the S of the distribution of the Central American Black Howler. A. p. trabeata Lawrence, 1933 — SW Panama (Azuero Peninsula).
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. Lowlands of EC Ethiopia (Awash area) and NW Somalia. The exact southern limit of the Northern Lesser Kudu''s distribution in eastern Ethiopia requires additional research. in Bovidae
Distribution. Lowlands of EC Ethiopia (Awash area) and NW Somalia. The exact southern limit of the Northern Lesser Kudu''s distribution in eastern Ethiopia requires additional research.
Distribution. Two disjunct areas across the lowland rainforest belt of W Africa (Guinea, Sierra Leone, Liberia, Ivory Coast, Ghana, Togo & Benin) and C Africa through the Congo Basin (Cameroon, Gabon, Republic of the Congo, DR Congo, Central African Republic & extreme SW Sudan), and five very small disjunct populations in mountainous areas in C Kenya. in Bovidae
Distribution. Two disjunct areas across the lowland rainforest belt of W Africa (Guinea, Sierra Leone, Liberia, Ivory Coast, Ghana, Togo & Benin) and C Africa through the Congo Basin (Cameroon, Gabon, Republic of the Congo, DR Congo, Central African Republic & extreme SW Sudan), and five very small disjunct populations in mountainous areas in C Kenya.
Distribution. NE Pakistan, lowland areas of S Nepal, and Peninsular India. Introduced into Italy near Rome (extirpated during World War II), South Africa, S USA (Texas), and N Mexico (Coahuila, Nuevo Leon, Sonora, Tamaulipas & Veracruz). in Bovidae
Distribution. NE Pakistan, lowland areas of S Nepal, and Peninsular India. Introduced into Italy near Rome (extirpated during World War II), South Africa, S USA (Texas), and N Mexico (Coahuila, Nuevo Leon, Sonora, Tamaulipas & Veracruz).
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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.