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.
310
datasets available to search
ShareScore release 0.9.0
Dataset results
310 results for “Caribbean Islands”
FIGURE 8 in Two new species of Triozocera Pierce, 1909 (Insecta: Strepsiptera: Corioxenidae) from the Caribbean Islands
FIGURE 8. Head of Triozocera macrognathus n. sp. Scale bar = 0.1 mm.
FIGURE 6 in Two new species of Triozocera Pierce, 1909 (Insecta: Strepsiptera: Corioxenidae) from the Caribbean Islands
FIGURE 6. Hind Wing and wing veins of Triozocera albocciput n. sp.
FIGURE 7 in Two new species of Triozocera Pierce, 1909 (Insecta: Strepsiptera: Corioxenidae) from the Caribbean Islands
FIGURE 7. Aedeagus of Triozocera albocciput n. sp. Scale bar = 0.1 mm.
FIGURE 2 in Two new species of Triozocera Pierce, 1909 (Insecta: Strepsiptera: Corioxenidae) from the Caribbean Islands
FIGURE 2. Antenna of Triozocera albocciput n. sp. Scale bar = 0.1 mm.
FIGURE 1 in Two new species of Triozocera Pierce, 1909 (Insecta: Strepsiptera: Corioxenidae) from the Caribbean Islands
FIGURE 1.Head of Triozocera albocciput n. sp. Scale bar = 0.1 mm.
FIG. 1 in Distribution of potentially toxic epiphytic dinoflagellates in Saint Martin Island (Caribbean Sea, Lesser Antilles)
FIG. 1. — Distribution of potentially toxic benthic dinoflagellates abundances (cells g–1) in Saint Martin Island.
FIGURE 18. Tethysimyia species A in A first account of Chyromyidae (Diptera: Acalyptratae) from continental Central and South America and some Caribbean Islands, with descriptions of new species
FIGURE 18. Tethysimyia species A from Bonaire, wing.
Data from: Population genomic analysis uncovers African and European admixture in Drosophila melanogaster populations from the southeastern United States and Caribbean Islands
Open the record for dataset details and reuse information.
Data from: Adaptive introgression from distant Caribbean islands contributed to the diversification of a microendemic adaptive radiation of trophic specialist pupfishes
Rapid diversification often involves complex histories of gene flow that leave variable and conflicting signatures of evolutionary relatedness across the genome. Identifying the extent and source of variation in these evolutionary relationships can provide insight into the evolutionary mechanisms involved in rapid radiations. Here we compare the discordant evolutionary relationships associated with species phenotypes across 42 whole genomes from a sympatric adaptive radiation of Cyprinodon pupfishes endemic to San Salvador Island, Bahamas and several outgroup pupfish species in order to understand the rarity of these trophic specialists within the larger radiation of Cyprinodon. 82% of the genome depicts close evolutionary relationships among the San Salvador Island species reflecting their geographic proximity, but the vast majority of variants fixed between specialist species lie in regions with discordant topologies. Top candidate adaptive introgression regions include signatures of selective sweeps and adaptive introgression of genetic variation from a single population in the northwestern Bahamas into each of the specialist species. Hard selective sweeps of genetic variation on San Salvador Island contributed 5 times more to speciation of trophic specialists than adaptive introgression of Caribbean genetic variation; however, four of the 11 introgressed regions came from a single distant island and were associated with the primary axis of oral jaw divergence within the radiation. For example, standing variation in a proto-oncogene (ski) known to have effects on jaw size introgressed into one San Salvador Island specialist from an island 300 km away approximately 10 kya. The complex emerging picture of the origins of adaptive radiation on San Salvador Island indicates that multiple sources of genetic variation contributed to the adaptive phenotypes of novel trophic specialists on the island. Our findings suggest that a suite of factors, including rare adaptive introgression, may be necessary for adaptive radiation in addition to ecological opportunity.
Using Mobile Phone Text Messaging System to Improve Exclusive Breastfeeding Rate in a Resource-poor Caribbean Island
ClinicalTrials.gov study NCT03853850. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Caribbean Island Urinary Iodine Survey 2018
ClinicalTrials.gov study NCT04388540. IPD Sharing: Not stated. Countries: 10. Publications: 0.
Data from: Adaptive introgression from distant Caribbean islands contributed to the diversification of a microendemic adaptive radiation of trophic specialist pupfishes
Open the record for dataset details and reuse information.
FIGURES 1–16. 1–2 in Key to Mexican and Central American genera of Acanthocinini (Coleoptera Cerambycidae, Lamiinae) with erect setae on elytral surface, excluding the Caribbean Islands
FIGURES 1–16. 1–2) Alcidion humerale (Perty, 1832), male, Brazil (S"o Paulo) (from Monné et al. 2020): 1) Dorsal habitus; 2) Ventral habitus. 3) Amniscus praemorsus (Fabricius, 1793), lectotype, dorsal habitus (by Jesus Santiago Moure). 4) Antecrurisa apicalis (Bates, 1864), holotype, dorsal habitus (by Jesus Santiago Moure). 5) Baryssinus penicillatus Bates, 1864, holotype, dorsal habitus (by Jesus Santiago Moure). 6) Baryssinus bicirrifer Bates, 1872, holotype, dorsal habitus (by Jesus Santiago Moure). 7) Canidia canescens (Dillon, 1955), paratype, dorsal habitus (by Jesus Santiago Moure). 8) Carphina occulta Monné, 1990, paratype male, dorsal habitus (from Monné et al. 2020). 9) Cosmotoma adjuncta (Thomson, 1860), male, dorsal habitus, Brazil (Pará) (from Monné et al. 2020). 10) Dectes texanus LeConte, 1862, holotype, dorsal habitus (by Jesus Santiago Moure). 11) Eutrichillus comus (Bates, 1881), holotype, dorsal habitus (by Jesus Santiago Moure). 12) Glaucotes yuccivorous (Fall, 1907), syntype, dorsal habitus (from Bezark 2020). 13) Granastyochus elegantissimus (Tippmann, 1953), female, dorsal habitus, Peru (from Monné et al. 2020). 14) Graphisurus eucharis (Bates, 1885), holotype, dorsal habitus (by Jesus Santiago Moure). 15) Graphisurus vexillaris (Bates, 1872), lectotype female, dorsal habitus (by Jesus Santiago Moure). 16) Leptocometes hispidus Bates, 1881, male, dorsal habitus, Mexico (Chiapas) (from Monné et al. 2020).
FIGURE 30 in A new skink fauna from Caribbean islands (Squamata, Mabuyidae, Mabuyinae) 3288
FIGURE 30. Head scalation in species of the Genus Mabuya (left, side view; right, dorsal view). (A) M. cochonae sp. nov. (KU 242043, holotype); (B) M. desiradae sp. nov. (KU 242045, holotype); (C) M. dominicana (MCZ R-182281); and (D) M.
FIGURE 23 in A new skink fauna from Caribbean islands (Squamata, Mabuyidae, Mabuyinae) 3288
FIGURE 23. Head scalation in species of the Genus Copeoglossum occupying Caribbean islands (left, side view; right, dorsal view). (A) C. aurae sp. nov. (BMNH 90.11.25.16, paratype); (B) C. margaritae sp. nov. (USNM 217141, holotype); and (C) C. redondae sp. nov. (ANSP 9517, holotype).
FIGURE 48 in A new skink fauna from Caribbean islands (Squamata, Mabuyidae, Mabuyinae) 3288
FIGURE 48. Marisora aurulae sp. nov., from the Lesser Antilles: (A–B) MCZ R-38196, holotype, Young's Island, St. Vincent; (C) MCZ R-79098, paratype, Carriacou, Grenadines; (D) MCZ R-12079, Tobago (no specific locality). Marisora falconensis, from Venezuela: (E) CM 7985, Sucre, Elvecia.
FIGURE 27 in A new skink fauna from Caribbean islands (Squamata, Mabuyidae, Mabuyinae) 3288
FIGURE 27. Graph of suture length between supraocular-2 and supraciliaries versus that between supraocular-1 and supraciliaries in four species of the Genus Copeoglossum. Copeoglossum arajara is not included because it has three supraoculars, possibly from fusion between first and second supraoculars.
FIGURE 11 in A new skink fauna from Caribbean islands (Squamata, Mabuyidae, Mabuyinae) 3288
FIGURE 11. Map showing the distribution of mabuyine skinks occurring in the Lesser Antilles and Trinidad and Tobago. See Fig. 1 for location of the islands. The islands and species are: (A) Anguilla, Dog Island, and St. Barts (Spondylurus powelli sp. nov., squares), and St. Martin (S. martinae sp. nov., circle); (B) Guadeloupe: Basse-Terre (Mabuya guadeloupae sp. nov., square), Grande-Terre (Mabuya grandisterrae sp. nov., triangle), Îlet à Cochons (Mabuya cochonae sp. nov., star), La Désirade and Terre de Bas, Petite-Terre (Mabuya desiradae sp. nov., diamonds), and Marie-Galante (Capitellum mariagalantae sp. nov., circle); (C) Martinique (Mabuya mabouya, circles; Capitellum metallicum, triangle); (D) St. Vincent, the Grenadines, and Grenada (Copeoglossum aurae sp. nov., circles; Marisora aurulae sp. nov., triangles); (E) Redonda (Copeoglossum redondae sp. nov., circle) and Montserrat (Mabuya montserratae sp. nov., square); (F) Dominica (Mabuya dominicana); (G) St. Lucia (Alinea luciae), (H) Barbados (Alinea lanceolata); (I) Trinidad (Copeoglossum aurae sp. nov., circles; Marisora aurulae sp. nov., triangle), and (J) Tobago (Copeoglossum aurae sp. nov., circles; Marisora aurulae sp. nov., triangles). Hollow symbols in A and J are literature records (specimens not examined). Where no specific localities within an island are known for a species, a symbol is placed centrally on the island: Alinea luciae, Capitellum mariagalantae, Capitellum metallicum, and Copeoglossum redondae sp. nov. The scale in (A) applies to all islands.
FIG. 1 in Deciphering Geographical Affinity and Reconstructing Invasion Scenarios of Boa imperator on the Caribbean Island of Cozumel
FIG. 1. Map depicting sampling localities for Boa imperator from (A) continental mainland and (B) Cozumel Island. Squares indicate individuals from the Gulf of Mexico clade (n ¼ 14; see Results and Fig. 2), circles from the Yucatán Peninsula clade (n ¼ 16), and diamonds from Cozumel (n ¼ 16). Colors follow the ODC haplotype network population nomenclature (Fig. 3).
FIG. 4 in Deciphering Geographical Affinity and Reconstructing Invasion Scenarios of Boa imperator on the Caribbean Island of Cozumel
FIG. 4. Neighbor-net haplotype network based on 41 unique nuclear ODC haplotypes within Boa imperator.
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.