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.
888
datasets available to search
ShareScore release 0.9.0
Dataset results
888 results for “Canary”
FIGURE 1 in A new cavernicolous assassin bug from the Canary Islands (Hemiptera: Reduviidae: Emesinae: Collartidini)
FIGURE 1. Habitus of macropterous male of Collartida phantasma sp. nov. (holotype).
Distribution. Canary Is, on Tenerife, La Palma, and El Hierro; probably also La Gomera. in Vespertilionidae
Distribution. Canary Is, on Tenerife, La Palma, and El Hierro; probably also La Gomera.
Temporal and palaeoclimatic context of the evolution of insular woodiness in the Canary Islands: Supplementary tables and figures
<p>Insular woodiness (IW), referring to the evolutionary transition from herbaceousness towards woodiness on islands, has arisen more than 30 times on the Canary Islands (Atlantic Ocean). One of the IW hypotheses suggests that drought has been a major driver of wood formation, but we do not know in which palaeoclimatic conditions the insular woody lineages originated. Therefore, we provided an updated review on the presence of IW on the Canaries, reconstructed the palaeoclimate, and estimated the timing of origin of woodiness of 24 insular woody lineages that represent a large majority of the insular woody species diversity on the Canaries. Our single, broad-scale dating analysis shows that woodiness in 60-65% of the insular woody lineages studied originated within the last 3.2 Myr, during which Mediterranean seasonality (yearly summer droughts) became established on the Canaries. Consequently, our results are consistent with palaeoclimatic aridification as a potential driver of woodiness in a considerable proportion of the insular woody Canary Island lineages. However, the observed pattern between insular woodiness and palaeodrought during the last couple of million years could potentially have emerged as a result of the typically young age of the native insular flora, characterised by a high turnover.</p>
Dated tree of 24,000 Angiosperms species incl Canary Island colonisation events
<p><span><span><span><span><span><span><span><span><span><span><span>Insular woodiness (IW), referring to the evolutionary transition from herbaceousness towards woodiness on islands, has arisen more than 30 times on the Canary Islands (Atlantic Ocean). One of the IW hypotheses suggests that drought has been a major driver of wood formation, but we do not know in which palaeoclimatic conditions the insular woody lineages originated. Therefore, we provided an updated review on the presence of IW on the Canaries, reconstructed the palaeoclimate, and estimated the timing of origin of woodiness of 24 insular woody lineages that represent a large majority of the insular woody species diversity on the Canaries. Our single, broad-scale dating analysis shows that woodiness in 60-65% of the insular woody lineages studied originated within the last 3.2 Myr during which Mediterranean seasonality (yearly summer droughts) became established on the Canaries. Consequently, our results are consistent with palaeoclimatic aridification as a potential driver of woodiness in a considerable proportion of the insular woody Canary Island lineages. However, the observed pattern between insular woodiness and palaeodrought during the last couple of million years could potentially have emerged as a result of the typically young age of the native insular flora that is characterised by a high turnover.</span></span></span></span></span></span></span></span></span></span></span></p>
FIGURE 1 in The Polycladida (Platyhelminthes) of the Canary Islands. New genus, species and records
FIGURE 1. Sampling station of the Canary Islands (for explanation of legends see Table 1).
Figure 4 from: Quijada L, Baral H-O (2017) Orbilia beltraniae, a new succulenticolous species from the Canary Islands. MycoKeys 25: 1-12. https://doi.org/10.3897/mycokeys.25.13917
Figure 4 - Morphological features of species related to Orbilia beltraniae. 1 Orbilia cardui 2 Orbilia cotoneastri 3 Orbilia rectispora. a Fresh apothecia b Paraphyses c Excipular tissues in median section d–e. Ascospores. Scale bars: 500 µm= 1a, 2a, 3a; 50 µm= 1c, 3b; 10 µm= 1b, d, 2b–d, 3c–e. All mounted in H2O. Photos: H.B. 7241a = 2a; H.B. 9549 = 3b, d; H.B. 9645b = 2b, d; H.B. 9891 = 1a, c–d; H.B. 9901 = 1b; H.B. 9962 = 3a, c, e; J.P.P. 28122 = 2c.
Figure 2 from: Quijada L, Baral H-O (2017) Orbilia beltraniae, a new succulenticolous species from the Canary Islands. MycoKeys 25: 1-12. https://doi.org/10.3897/mycokeys.25.13917
Figure 2 - Bayesian 50% majority rule consensus tree based on a concatenated alignment of ITS and LSU sequences of 42 strains of Orbiliaceae(see Table 1). Bold branches were supported by ML bootstrap values ≥75% and BI PP≥0.95. Subgroups within section Arthrobotrys have been recognised by other authors in five different genera according to their asexual states and trapping devices: I Dactylella II Drechslerella III Arthrobotrys IV Dactylellina V Gamsylella. * = name at present not validly published (Baral et al. 2017a).
Figure 3 from: Quijada L, Baral H-O (2017) Orbilia beltraniae, a new succulenticolous species from the Canary Islands. MycoKeys 25: 1-12. https://doi.org/10.3897/mycokeys.25.13917
Figure 3 - Morphological features of Orbilia beltraniae. 1 Apothecia rehydrated after 1–2 weeks 2 Excipular tissues in median section 3 Paraphyses 4 Asci 5 Ascospores. Scale bars: 500 µm= 1a–k; 50 µm= 2a; 10 µm= 2b–c, 3a, c, g, 4e, 5a–e; 5 µm= 3b, d–f, 4a–d, 5f; Mounted in: CR= 3b–d, 4b, d, 5d; H2O= 2a–c, 3a, e–g, 4a, c, e, 5a–c, e–g. Photos: TFC Mic. 23771 = 1i–k, 3b–c, 4b, 5a; TFC Mic. 23836 = 1h, 2c, 3d–e, 5b; TFC Mic. 23890 = 1d–e, 4a, 5f; TFC Mic. 23902 = 1f–g, 3a, 4c; TFC Mic. 24231 = 2a, 3g, 5c, g; TFC Mic. 24363 =1c, 2b, 3f, 4d–e, 5d–e; TFC Mic. 24449 = 1a–b.
Figure 1 from: Quijada L, Baral H-O (2017) Orbilia beltraniae, a new succulenticolous species from the Canary Islands. MycoKeys 25: 1-12. https://doi.org/10.3897/mycokeys.25.13917
Figure 1 - Monitored localities in Euphorbia scrubs: number of locality, place name for locality according to IDECanarias visor 3.0 (http://visor.grafcan.es/visorweb/), latitude, longitude, and altitude. In yellow the localities where Orbilia beltraniae was found.
Figure 3 from: Macías-Hernández N, López SC, Roca-Cusachs M, Oromí P, Arnedo MA (2016) A geographical distribution database of the genus Dysdera in the Canary Islands (Araneae, Dysderidae). ZooKeys 625: 11-23. https://doi.org/10.3897/zookeys.625.9847
Figure 3 - Graphical representation of the island endemisms and the species shared between islands. Pie sizes are proportional to the number of species on each island. Black sectors: number of species shared with other islands; grey sectors: proportion of local endemisms. Lines connecting pies: number of shared species between the corresponding islands, the width of the lines being proportional to the number of shared species. The disposition of pies reflects the geographical arrangement of the islands: P: La Palma, H: El Hierro, G: La Gomera, T: Tenerife, C: Gran Canaria, F: Fuerteventura, L: Lanzarote.
Figure 1 from: Macías-Hernández N, López SC, Roca-Cusachs M, Oromí P, Arnedo MA (2016) A geographical distribution database of the genus Dysdera in the Canary Islands (Araneae, Dysderidae). ZooKeys 625: 11-23. https://doi.org/10.3897/zookeys.625.9847
Figure 1 - Map of the Canary Islands showing their geological age according to Carracedo et al. (1998) and van den Bogaard (2013).
Figure 2 from: Macías-Hernández N, López SC, Roca-Cusachs M, Oromí P, Arnedo MA (2016) A geographical distribution database of the genus Dysdera in the Canary Islands (Araneae, Dysderidae). ZooKeys 625: 11-23. https://doi.org/10.3897/zookeys.625.9847
Figure 2 - Habitus of some Dysdera species: a Dysdera calderensis b Dysdera longa c Dysdera verneaui d Dysdera unguimmanis e Dysdera minutissima f Dysdera arabisenen g Dysdera sibyllina h Dysdera silvatica. Photographs by P. Oromí.
FIGURE 1 in Syllidae Grube, 1850 (Annelida) from Conception, Amanay and Banquete Banks off Canary Islands, with the description of two new species
FIGURE 1. Map of the Canary Islands, showing the sampling areas.
Fig. 1 in New records of Heteroptera from the Canary Islands (Spain), XI
Fig. 1.- Specimen of Amphiareus constrictus (Stṏl, 1860), El Jardín, near Los Realejos, Tenerife, Canary Islands, Spain. (Photo: Ben Jobson).
Fig. 1 in New records of Heteroptera from the Canary Islands (Spain), XII
Fig. 1.- Pseudopachybrachius reductus (Walker, 1872) (Heteroptera: Rhyparochromidae), La Laguna, Tenerife, Canary Islands, Spain. (Photo: Fernando Martín Melián Guerra).
Fig. 1 in New records of Heteroptera from the Canary Islands (Spain), VI
Fig. 1.– Adult specimen of Zelus renardii Kolenati, 1857, near Casillas de Morales, Fuerteventura, Canary Islands, Spain. (Photo: Diego Patiño).
Fig. 2 in New records of Heteroptera from the Canary Islands (Spain), IV
Fig. 2.- Nymph of Zelus renardii Kolenati, 1857, near Puerto del Carmen, Lanzarote, Canary Islands, Spai n. (Photo: Warren Stevens).
Fig. 1 in New records of Heteroptera from the Canary Islands (Spain), IV
Fig. 1.- Adult specimen of Zelus renardii Kolenati, 1857, Puerto Calero, Lanzarote, Canary Islands, Spain. (Photo: Warren Stevens).
Figure 1 from: Suárez D, Martín S, Naranjo M (2018) First report of the invasive alien species Caenoplana coerulea Moseley, 1877 (Platyhelminthes, Tricladida, Geoplanidae) in the subterranean environment of the Canary Islands. Subterranean Biology 26: 67-74. https://doi.org/10.3897/subtbiol.26.25921
Figure 1 A location of "La Federica" mine (red dot) within Gran Canaria (Canary Islands) B topography of the mine. C.coerulea individuals were observed in the red shaded area.
FIGURE 33A–B in The survey of Seira Lubbock, 1870 (Collembola, Entomobryidae, Seirinae) from Iberian Peninsula and Canary Islands, including three new species
FIGURE 33A–B. Seira betica sp. nov.: dorsal chaetotaxy; A, Abd IV; B, Abd V.
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.