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.
92
datasets available to search
ShareScore release 0.9.0
Dataset results
92 results for “Cape Verde Islands”
FIG. 10 in Gobiid ®shes from the Cape Verde Islands, including two new species of Gobius (Teleostei: Gobioidei)
FIG. 10. Mauligobius nigri, female, 70.0 1 16.0 mm, SaÄo Tiago: (A) multi®d free uppermost pectoral ®n-ray; (B) lateral snout with anterior and posterior nostrils; (C) pelvic disc. Abbreviations as ®gure 4; LL, lower lip.
FIG. 9 in Gobiid ®shes from the Cape Verde Islands, including two new species of Gobius (Teleostei: Gobioidei)
FIG. 9. Cape Verdes archipelago, showing occurrence of Gobius tetrophthalmus sp. nov. Closed circles: localities where collected; closed triangles: observed but not collected; open circles: not found.
FIG. 8 in Gobiid ®shes from the Cape Verde Islands, including two new species of Gobius (Teleostei: Gobioidei)
FIG. 8. Gobius tetrophthalmus sp. nov., male, 48.0 1 13.0 mm. Head lateral-line canal pores and sensory papillae in (A) lateral, and (B) dorsal views. Abbreviations as text.
FIG. 7 in Gobiid ®shes from the Cape Verde Islands, including two new species of Gobius (Teleostei: Gobioidei)
FIG. 7. Gobius tetrophthalmus sp. nov., male, 48.0 1 13.0 mm (BMNH). (A) pectoral ®n upper free rays; (B) lateral snout with anterior and posterior nostrils; (C) pelvic disc. Abbreviations as ®gure 4.
FIG. 6 in Gobiid ®shes from the Cape Verde Islands, including two new species of Gobius (Teleostei: Gobioidei)
FIG. 6. Gobius tetrophthalmus sp. nov., holotype, male, 62.5 1 15.0 mm (TFMC), Ilheu de Sal Rei, Boa Vista, in (A) lateral, (B) dorsal, and (C) ventral views.
FIG. 5 in Gobiid ®shes from the Cape Verde Islands, including two new species of Gobius (Teleostei: Gobioidei)
FIG. 5. Gobius ateriformis sp. nov., holotype, male, 55.5 1 12.0 mm (BMNH), Sa Äo Tiago. Head lateral-line canal pores and sensory papillae in (A) lateral, and (B) dorsal views. Abbreviations as text.
FIG. 4 in Gobiid ®shes from the Cape Verde Islands, including two new species of Gobius (Teleostei: Gobioidei)
FIG. 4. Gobius ateriformis sp. nov., holotype, male, 55.5 1 12.0 mm (BMNH), Sa Äo Tiago: (A) pectoral ®n upper free rays; (B) lateral snout with anterior and posterior nostrils; (C) pelvic disc. A, anus; AM, anterior pelvic membrane; AN, PN, anterior and posterior nostrils; E, eye; S, canal pore; UL, upper lip.
FIG. 3 in Gobiid ®shes from the Cape Verde Islands, including two new species of Gobius (Teleostei: Gobioidei)
FIG. 3. Gnatholepis thompsoni. Head lateral-line canal pores and sensory papillae of male, 29.51 9.0 mm, SaÄo Tiago, in (A) lateral, (B) dorsal, and (C) mental views; (D) anterior membrane of pelvic disc, with villose free edge, in female, 40.5 1 12.0 mm, Sal Rei, Boa Vista. Abbreviations as text.
FIG. 2 in Gobiid ®shes from the Cape Verde Islands, including two new species of Gobius (Teleostei: Gobioidei)
FIG. 2. (A) Gnatholepis thompsoni, male, 43.01 13.0 mm, SaÄo Vicente; (B) Gobius ateriformis sp. nov., holotype, male, 55.0 1 12.0 mm (BMNH), Sa Äo Tiago; (C) Mauligobius nigri, female, 70.0 1 16.0 mm, SaÄo Tiago.
FIG. 1 in Gobiid ®shes from the Cape Verde Islands, including two new species of Gobius (Teleostei: Gobioidei)
FIG. 1. Didogobius kochi, dark phase; (B) D. kochi, paler phase retaining prominent anterior vertical dark band; (C) Gobius ateriformis sp. nov.; (D) Gobius tetrophthalmus sp. nov. All from Ilheu do Sal Rei, Boa Vista.
Figure 4. Discriminant analyses for males and females previously called T in An integrative taxonomic revision of the Tarentola geckos (Squamata, Phyllodactylidae) of the Cape Verde Islands
Figure 4. Discriminant analyses for males and females previously called T. darwini. The total contribution of each of the two Canonical Discriminant Functions (CDF1 and CDF2) to explain the total morphological variation is also given. See Material and methods for details.
Figure 2 in An integrative taxonomic revision of the Tarentola geckos (Squamata, Phyllodactylidae) of the Cape Verde Islands
Figure 2. Phylogenetic relationships of endemic Cape Verde Tarentola taxa and their relatives from the Canary Islands modified from Vasconcelos et al. (2010) based on cytochrome b and 12S rRNA genes. The tree was inferred using maximum likelihood (ML) and GTR+I+G model of sequence evolution (log likelihood = -6468.896) and was rooted using Tarentola americana. Bootstrap support values above 60% for the ML analysis are shown below nodes. Posterior probability (PP) values higher than 95% for the Bayesian analysis are represented by an asterisk (*) and are shown above nodes. Names in bold follow the new taxonomic proposal and non-bold ones the taxonomy accepted in previous recent papers (Carranza et al., 2000; Jesus et al., 2002; Vasconcelos et al., 2010). For further details see Vasconcelos et al. (2010). Characters immediately to the right of island names correspond to the 15 evolutionarily significant units (ESUs) of A, B, C, and D clades recognized in the present work and represented in split green bars. Lines of evidence (in grey): 1, mitochondrial DNA (independent cyt b parsimony networks with a connection limit of 95%; see Appendix 3); 2, nuclear DNA (absence of shared haplotypes in MC1R); 3, morphology (detection of any diagnostic morphological character or a set of a unique combination of characters). Integration approaches (in red) from the most conservative to the most inflationist: ITC stands for integration by total congruence (all lines of evidence should be congruent), IPC stands for integration by partial congruence, retained in the present study (at least two lines of evidence are necessary); IC stands for integration by cumulation (one line of evidence is sufficient). Species are represented in split red bars and subspecies in yellow.
Figure 3 in An integrative taxonomic revision of the Tarentola geckos (Squamata, Phyllodactylidae) of the Cape Verde Islands
Figure 3. Parsimony networks corresponding to the PDC, ACM4 and MC1R nDNA sequence variation in Tarentola from the Cape Verde Islands. Lines represent a mutational step, circles haplotypes and dots missing haplotypes. The size of circles is proportional to the number of haplotypes and colours to the number of individuals. The dotted circles represent the most probable ancestral haplotype. Samples from the same island are similarly coloured but with different tonalities for different taxa. For correspondences of sample and location codes see Appendix 1.
Figure 7 in An integrative taxonomic revision of the Tarentola geckos (Squamata, Phyllodactylidae) of the Cape Verde Islands
Figure 7. Photographs of the dorsal and lateral views of Tarentola of the Cape Verde Islands. A1, T. boavistensis; A2, T. bocagei; A3, T. fogoensis; A4, T. darwini; B1, T. substituta; B2, T. raziana; B3, T. caboverdiana; C, T. nicolauensis; D1, T. gigas (T. gigas brancoensis on the left and T. gigas gigas on the right); D2, T. rudis; D3, T. protogigas protogigas; D4, T. p. hartogi from Brava Island; D5, T. p. hartogi from Rombos Islets; D6, T. maioensis.
Figure 1 in An integrative taxonomic revision of the Tarentola geckos (Squamata, Phyllodactylidae) of the Cape Verde Islands
Figure 1. Map of the Cape Verde Islands showing the geographical location (latitudes and longitudes) and altitudes of the islands and the origins of the new Tarentola samples included in the genetic (circles) and morphological (diamonds) analyses (Geographic Coordinate System, Datum WGS 84). Island and taxa colours match the colours used on the network analyses. No specimens were found on Sal.
Figure 6 in An integrative taxonomic revision of the Tarentola geckos (Squamata, Phyllodactylidae) of the Cape Verde Islands
Figure 6. Typical dorsal patterns of Tarentola species of the Cape Verde Islands (adapted from Joger, 1993).
FIGURE 1 in Pollicipes caboverdensis sp. nov. (Crustacea: Cirripedia: Scalpelliformes), an intertidal barnacle from the Cape Verde Islands
FIGURE 1. Pollicipes caboverdensis sp. nov., Cape Verde Islands. View from the left side.
Table 1 in Molecular analysis reveals a cryptic species of Chthamalus (Crustacea: Cirripedia) in the Cape Verde Islands
<p><b>Table 1.</b> Number of individuals for each marker</p><table><tbody><tr><th><i>Chthamalus</i> species</th><th><i>EF1</i></th><th><i>NaKA</i></th><th><i>COI</i></th></tr></tbody><tbody><tr><th><i>C. alani</i></th><td>24</td><td>8</td><td>19</td></tr><tr><th><i>C. angustitergus</i></th><td>18</td><td>7</td><td>23</td></tr><tr><th><i>C. dalli</i></th><td>8</td><td>8</td><td>164</td></tr><tr><th><i>C. fissus</i></th><td>10</td><td>6</td><td>12</td></tr><tr><th><i>C. hedgecocki</i></th><td>10</td><td>8</td><td>9</td></tr><tr><th><i>C. panamensis</i></th><td>19</td><td>9</td><td>33</td></tr><tr><th><i>C. proteus</i></th><td>16</td><td>9</td><td>22</td></tr><tr><th><i>C. stellatus</i></th><td>236</td><td>233</td><td>61</td></tr><tr><th>Cape Verde population</th><td>37</td><td>37</td><td>12</td></tr><tr><th>Total</th><td>378</td><td>325</td><td>355</td></tr></tbody></table>
Figure 7 in Molecular analysis reveals a cryptic species of Chthamalus (Crustacea: Cirripedia) in the Cape Verde Islands
Figure 7. Shell and opercular valves redrawn from Darwin (1854: plate XVIII 1a, 1f).
Lagrangian trajectories representing surface drift from the Cape Verde islands
<p><strong>Example trajectories from a biophysical Lagrangian simulation</strong></p> <p>This is 25x 10.000 example trajectories from biophysical experiments performed with Parcels.</p> <p>The trajectories are a tiny subset of a much bigger collection of trajectories that have been simulated with the aim of learning about the fate of particles drifting away from the Cape Verde islands.</p> <p><em>Note, that these trajectories should not be used for biological or physical science but merely serve as study objects for developing, testing, or benchmarking (stasticical) methods and algorithms.</em></p> <p><strong>Details of the experiments</strong></p> <p>The trajectories are taken from 25 sets of biophysical simulations which differ in the year they represent. Particles are seeded between mid of August and start of December of the years 1993 to 2017. They are subject to Ocean surface currents simulated by a high-resolution ocean model and subject to Stokes Drift estimated by a wave simulation data provided by the Copernicus Marine Service (<a href="https://marine.copernicus.eu/">https://marine.copernicus.eu/</a>).</p> <p><strong>Data</strong></p> <p>The full data come as a Zarr store inside of a ZIP file <code>cape_verde_drift_trajectories_1993-2017.zarr.zip</code> which you need to download and unzip to be able to read it, e.g., with Xarray's <code>open_zarr</code> method. There are subsets of 10000 trajectories provided as compressed csv files split into years called <code>cape_verde_drift_trajectories_1-10000_1993.csv.gz</code> ... <code>cape_verde_drift_trajectories_1-10000_2017.csv.gz</code>. And there are subsets of 100 trajectories provided as un-compressed csv files split into years <code>called cape_verde_drift_trajectories_1-100_1993.csv</code> ... <code>cape_verde_drift_trajectories_1-100_2017.csv</code>.</p> <p><strong>Variables and their meaning</strong></p> <ul> <li><code>"obs"</code> contains the time step since the larva started to exist. Each trajectory covers up to 881 daily positions.</li> <li><code>"traj"</code> indicates the trajectory ID.</li> <li><code>"lat"</code> and <code>"lon"</code> contain the horizontal positions in degrees Latitude and Longitude.</li> <li><code>"temp"</code> contains the ambient temperature in degrees Celsius the simulated larva would have felt.</li> <li><code>"time"</code> contains time stamps for each position.</li> <li><code>"z"</code> contains the vertical positions of the simulated larva in meters counted downwards. As <code>"z</code>" does not vary (all particles are at the surface), it is omitted from the CSV files.</li> </ul> <p><strong>Details on the subsetting</strong></p> <p>See <a href="https://nbviewer.org/urls/zenodo.org/record/6826071/files/cape_verde_turtle_subsetting.ipynb">cape_verde_turtle_subsetting.ipynb</a>.</p> <p><strong>Using the data</strong></p> <p>This data set is licensed under a <em>Creative Commons Attribution 4.0 International License</em>.</p> <p>If you use the data, we'd love to get a notice to <a href="mailto:wrath@geomar.de">wrath@geomar.de</a>. This is, however, not required.</p>
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.