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.
13
datasets available to search
ShareScore release 0.9.0
Dataset results
13 results for “Coastal lowlands”
Evaluation of flood hazards in data-sparse coastal lowlands: highlighting the Ayeyarwady Delta (Myanmar)
<p>This folder includes datasets that were produced to assess flood hazards and exposure in the Ayeyarwady Delta in Myanmar by applying the new standardised, integrative approach of Seeger, K., Peffeköver, A., Minderhoud, P. S. J., Vogel, A., Brückner, H., Kraas, F., Nay Win Oo, Brill, D. (2024):<br>Evaluating flood hazards in data-sparse coastal lowlands: highlighting the Ayeyarwady Delta (Myanmar). Environmental Research Letters.<br>The README includes the names of files to be used for citation as well as a brief explanation when necessary. All processing details are given in the paper and related supplementary material.</p>
Subspecies and Distribution. A. g. geoffroyi Kuhl, 1820 — S & SE Nicaragua (coastal region around San Juan del Norte or Martina Bay, probably ranging across the lowlands to the vicinity of Lake Managua and Lake Nicaragua on the Pacific coast); possibly in N Costa Rica. A. g. azuerensis Bole, 1937 — SC Panama, known only from the forested mountains of the W side of the Azuero Peninsula (Veraguas Province) in the vicinity of Ponuga, where it appears to be isolated; it may also occur to the W along the Pacific coastto the Burica Peninsula, near the Panamanian and Costa Rican border. A. g. frontatus Gray, 1842 — N & W Nicaragua and NW Costa Rica. A. g. grisescens Gray, 1866 — S Panama along the Pacific coast in the valley of the Rio Tuyra and SE through the Serrania del Sapo of extreme SE Panama into the Cordillera de Baudo of NW Colombia. A. g. ornatus Gray, 1871 — C & E Costa Rica, and Panama (from Chiriqui Province to the Serrania de San Blas E of the Canal Zone). A. g. vellerosus Gray, 1866 — E & SE Mexico (E San Luis Potosi, Veracruz, Tabasco, E Oaxaca, and Chiapas states), Guatemala (including the highlands), El Salvador, and Honduras (along the N coastto the lowlands of La Mosquitia in Gracias a Dios Department). A. g. yucatanensis Kellogg & Goldman, 1944 — SE Mexico (forests of the Yucatan Peninsula), NE Guatemala, and adjoining parts of Belize; intergrading in S Mexico (Campeche State) and Guatemala with vellerosus. in Atelidae
Subspecies and Distribution. A. g. geoffroyi Kuhl, 1820 — S & SE Nicaragua (coastal region around San Juan del Norte or Martina Bay, probably ranging across the lowlands to the vicinity of Lake Managua and Lake Nicaragua on the Pacific coast); possibly in N Costa Rica. A. g. azuerensis Bole, 1937 — SC Panama, known only from the forested mountains of the W side of the Azuero Peninsula (Veraguas Province) in the vicinity of Ponuga, where it appears to be isolated; it may also occur to the W along the Pacific coastto the Burica Peninsula, near the Panamanian and Costa Rican border. A. g. frontatus Gray, 1842 — N & W Nicaragua and NW Costa Rica. A. g. grisescens Gray, 1866 — S Panama along the Pacific coast in the valley of the Rio Tuyra and SE through the Serrania del Sapo of extreme SE Panama into the Cordillera de Baudo of NW Colombia. A. g. ornatus Gray, 1871 — C & E Costa Rica, and Panama (from Chiriqui Province to the Serrania de San Blas E of the Canal Zone). A. g. vellerosus Gray, 1866 — E & SE Mexico (E San Luis Potosi, Veracruz, Tabasco, E Oaxaca, and Chiapas states), Guatemala (including the highlands), El Salvador, and Honduras (along the N coastto the lowlands of La Mosquitia in Gracias a Dios Department). A. g. yucatanensis Kellogg & Goldman, 1944 — SE Mexico (forests of the Yucatan Peninsula), NE Guatemala, and adjoining parts of Belize; intergrading in S Mexico (Campeche State) and Guatemala with vellerosus.
Distribution. The Guianas (E of the Essequibo River, but excluding the lowland coastal plains) and NE Brazil (N of the Rio Amazonas and E of the rios Negro and Branco); its occurrence W of the Essequibo and in Venezuela is doubtful. in Atelidae
Distribution. The Guianas (E of the Essequibo River, but excluding the lowland coastal plains) and NE Brazil (N of the Rio Amazonas and E of the rios Negro and Branco); its occurrence W of the Essequibo and in Venezuela is doubtful.
Distribution. Known from only two localities in the coastal lowlands of WC Ecuador (Los Rios and Guayas provinces). in Molossidae
Distribution. Known from only two localities in the coastal lowlands of WC Ecuador (Los Rios and Guayas provinces).
Subspecies and Distribution. T:s.stankoviciV.Martino&E.Martino,1931—WMacedoniaandadjacentNWGreeceMts. T. s. montenegrina Krystufek, 1994 — restricted to coastal lowlands of S Montenegro and adjacent Albania. Also present in C & S Albania and W Greece as far S as N Peloponnese, also on Corfu I in the Ionian Sea, but subspecies involved not known. in Talpidae
Subspecies and Distribution. T:s.stankoviciV.Martino&E.Martino,1931—WMacedoniaandadjacentNWGreeceMts. T. s. montenegrina Krystufek, 1994 — restricted to coastal lowlands of S Montenegro and adjacent Albania. Also present in C & S Albania and W Greece as far S as N Peloponnese, also on Corfu I in the Ionian Sea, but subspecies involved not known.
Distribution. Pacific coastal lowlands of Ecuador and NW Peru. in Echimyidae
Distribution. Pacific coastal lowlands of Ecuador and NW Peru.
A holocenic and dynamic hybrid zone between two cactophilic Drosophila species in a coastal lowland plain of the Brazilian Atlantic Forest
<p>Hybridization and introgression are processes that contribute to shaping biological diversity. The factors promoting the formation of these processes are multiples but poorly explored in a biogeographical and ecological context. In the southeast coastal plain of the Brazilian Atlantic Forest, a hybrid zone was described between two closely related cactophilic species, <i>Drosophila antonietae</i> and <i>D. serido. </i>Here, we revisited and analyzed specimens from this hybrid zone to evaluate its temporal and spatial dynamic. We examined allopatric and sympatric populations of the flies using independent sources of data such as mitochondrial and nuclear sequences, microsatellite loci, morphometrics of wings and male genitalia, and climatic niche models. We also verified the emergence of the flies from necrotic tissues of collected cacti to verify the role of host association for the population dynamics. Our results support the existence of a hybrid zone due to secondary contact and limited to the localities where the two species are currently in contact. Furthermore, we detected asymmetric bidirectional introgression and the maintenance of the species integrity, ecological association, and morphological characters, suggesting selection and limited introgression. Considering our paleomodels, probably this hybrid zone is recent and the contact occurred during the Holocene to the present-day, favored by range expansion of their populations due to expansion of open and dry areas in eastern South America during palaeoclimatic and geomorphological events.</p>
Figure 3 from: Lewington R, Beveridge P, Renner M (2013) Lejeunea hodgsoniana, a newly described, long recognised Lejeunea (Jungermanniopsida, Lejeuneaceae) from lowland coastal forest habitats in New Zealand. PhytoKeys 29: 1-15. https://doi.org/10.3897/phytokeys.29.5376
Figure 3 - Type locality. Above. Regenerating native coastal bush. Below. Trunk of Melicytus ramiflorus showing the extensive mats of Lejeunea hodgsoniana resulting from confluent growth.
Figure 2 from: Lewington R, Beveridge P, Renner M (2013) Lejeunea hodgsoniana, a newly described, long recognised Lejeunea (Jungermanniopsida, Lejeuneaceae) from lowland coastal forest habitats in New Zealand. PhytoKeys 29: 1-15. https://doi.org/10.3897/phytokeys.29.5376
Figure 2 - Lejeunea hodgsoniana. A Shoot showing the underleaf with a deep narrow sinus and long narrow lobes, and well-developed lobules B Androecia C Spores D Stem cross-section E Seta cross-section F Apices of a sporophyte valve showing elaters and pseudoelaters G–I Leaf cells showing the variation in oil body density. (G stained).
Figure 1 from: Lewington R, Beveridge P, Renner M (2013) Lejeunea hodgsoniana, a newly described, long recognised Lejeunea (Jungermanniopsida, Lejeuneaceae) from lowland coastal forest habitats in New Zealand. PhytoKeys 29: 1-15. https://doi.org/10.3897/phytokeys.29.5376
Figure 1 - Lejeunea hodgsoniana – Morphological features. A and B Well-developed lobule C–E Lobules showing the variety of forms from the same stem F Shoot with androecia G Stem cross-section H Inflated perianth with emergent sporophyte I Perianth before enlargement of the sporophyte showing the lateral and ventral carinae J Leading shoot showing a terminal gynoecium and a subfloral innovation. (All from type.) A–D: lobules scale bar 0.1 mm, E: four lobules, scale bar 0.1 m, F: scale bar 1mm, G: scale bar 25 µm, H–I: scale bar is 0.5 mm and J scale bar 1 mm.
A holocenic and dynamic hybrid zone between two cactophilic Drosophila species in a coastal lowland plain of the Brazilian Atlantic Forest
Open the record for dataset details and reuse information.
Figure 4 from: Lewington R, Beveridge P, Renner M (2013) Lejeunea hodgsoniana, a newly described, long recognised Lejeunea (Jungermanniopsida, Lejeuneaceae) from lowland coastal forest habitats in New Zealand. PhytoKeys 29: 1-15. https://doi.org/10.3897/phytokeys.29.5376
Figure 4 - Indicative distribution. This map shows the known distribution of Lejeunea hodgsoniana.
Distribution. SE Brazil (Rio de Janeiro State), originally the majority ofthe lowland coastal region ofthe State below elevations of 300 m; today largely restricted to two municipalities Silva Jardim and Cabo Frio. in Callitrichiade
Distribution. SE Brazil (Rio de Janeiro State), originally the majority ofthe lowland coastal region ofthe State below elevations of 300 m; today largely restricted to two municipalities Silva Jardim and Cabo Frio.
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.