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.
437
datasets available to search
ShareScore release 0.7.1
Dataset results
437 results for “threatened species”
Figure 1 from: Assis L, von Schimonsky DM, Bichuette ME (2021) The first troglobitic Pseudochthonius Balzan, 1892 (Pseudoscorpiones, Chthoniidae) from the karst area of Serra do Ramalho, Brazil: a threatened species. Subterranean Biology 40: 109-128. https://doi.org/10.3897/subtbiol.40.77451
Figure 1 Map depicting the known distribution of Pseudochthonius ramalho sp. nov. in Gruna do Vandercir cave, located in Bahia state. The cave belongs to karst area in Jacaré formation, Bambuí group.
Figure 11 from: Assis L, von Schimonsky DM, Bichuette ME (2021) The first troglobitic Pseudochthonius Balzan, 1892 (Pseudoscorpiones, Chthoniidae) from the karst area of Serra do Ramalho, Brazil: a threatened species. Subterranean Biology 40: 109-128. https://doi.org/10.3897/subtbiol.40.77451
Figure 11 Comparison of morphology among some species of Pseudochthonius from Brazil A Holotype Pseudochthonius ramalho sp. nov. (troglobitic) (LES9601) and left chela (A1) BPseudochthonius strinatii (troglobitic) (LES9391) and pedipalp detail (B1) CPseudochthonius biseriatus (troglobitic) (LES9434) and pedipalp detail (C1) DPseudochthonius sp. (epigean) (LES9629) and pedipalp detail (D1) (Images: A D. M. von Schimonsky; A1–C1 L.B.R Fernandes; D–D1 M. E. Bichuette).
Figure 5 from: Assis L, von Schimonsky DM, Bichuette ME (2021) The first troglobitic Pseudochthonius Balzan, 1892 (Pseudoscorpiones, Chthoniidae) from the karst area of Serra do Ramalho, Brazil: a threatened species. Subterranean Biology 40: 109-128. https://doi.org/10.3897/subtbiol.40.77451
Figure 5 Pseudochthonius ramalho sp. nov. scanning electron images. Paratype female, habitus A dorsal view B ventral view C zoom in on the anterior margin of the carapace with eye spots denoted with red circle. (Images: Luciana B. R. Fernandes).
Figure 6 from: Assis L, von Schimonsky DM, Bichuette ME (2021) The first troglobitic Pseudochthonius Balzan, 1892 (Pseudoscorpiones, Chthoniidae) from the karst area of Serra do Ramalho, Brazil: a threatened species. Subterranean Biology 40: 109-128. https://doi.org/10.3897/subtbiol.40.77451
Figure 6 Pseudochthonius ramalho sp. nov. female paratype scanning electron images A detail on the right chelicera of serrula exterior and rallumB detail on the right pedipalp trichobothrium isb and ib, lateral C left pedipalp D detail on the left pedipalp teeth. (Images: L. B. R. Fernandes).
Figure 10 from: Assis L, von Schimonsky DM, Bichuette ME (2021) The first troglobitic Pseudochthonius Balzan, 1892 (Pseudoscorpiones, Chthoniidae) from the karst area of Serra do Ramalho, Brazil: a threatened species. Subterranean Biology 40: 109-128. https://doi.org/10.3897/subtbiol.40.77451
Figure 10 Morphological differences on the carapace of hypogean and epigean species of Pseudochthonius: eyes (denoted with red circle), and the narrowing of the posterior region of the carapace (marked with dashed line on the sides of the carapace) A hypogean P. ramalho sp. nov. (male) B epigean P. thibaudiC epigean P. arabicus.
Figure 3 from: Assis L, von Schimonsky DM, Bichuette ME (2021) The first troglobitic Pseudochthonius Balzan, 1892 (Pseudoscorpiones, Chthoniidae) from the karst area of Serra do Ramalho, Brazil: a threatened species. Subterranean Biology 40: 109-128. https://doi.org/10.3897/subtbiol.40.77451
Figure 3 Holotype of Pseudochthonius ramalho sp. nov. in natural habitat, at Gruna do Vandercir cave, Serra do Ramalho, Bahia. (Image: Adriano Gambarini).
Figure 9 from: Assis L, von Schimonsky DM, Bichuette ME (2021) The first troglobitic Pseudochthonius Balzan, 1892 (Pseudoscorpiones, Chthoniidae) from the karst area of Serra do Ramalho, Brazil: a threatened species. Subterranean Biology 40: 109-128. https://doi.org/10.3897/subtbiol.40.77451
Figure 9 Distribution of epigean and hypogean Pseudochthonius species in Brazil, with troglobitic representatives detached.
Supplementary material 2 from: Kenis M, Agboyi LK, Adu-Acheampong R, Ansong M, Arthur S, Attipoe PT, Baba A-SM, Beseh P, Clottey VA, Combey R, Dzomeku I, Eddy-Doh MA, Fening KO, Frimpong-Anin K, Hevi W, Lekete-Lawson E, Nboyine JA, Ohene-Mensah G, Oppong-Mensah B, Nuamah HSA, van der Puije G, Mulema J (2022) Horizon scanning for prioritising invasive alien species with potential to threaten agriculture and biodiversity in Ghana. NeoBiota 71: 129-148. https://doi.org/10.3897/neobiota.71.72577
Risk scores for potential invasive alien plant pests in Ghana
Supplementary material 1 from: Kenis M, Agboyi LK, Adu-Acheampong R, Ansong M, Arthur S, Attipoe PT, Baba A-SM, Beseh P, Clottey VA, Combey R, Dzomeku I, Eddy-Doh MA, Fening KO, Frimpong-Anin K, Hevi W, Lekete-Lawson E, Nboyine JA, Ohene-Mensah G, Oppong-Mensah B, Nuamah HSA, van der Puije G, Mulema J (2022) Horizon scanning for prioritising invasive alien species with potential to threaten agriculture and biodiversity in Ghana. NeoBiota 71: 129-148. https://doi.org/10.3897/neobiota.71.72577
Guidelines for horizon scanning for plant pests potentially threatening Ghana
Supplementary material 1 from: Karam-Gemael M, Izzo T, Chagas-Jr A (2018) Why be red listed? Threatened Myriapoda species in Brazil with implications for their conservation. In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 255-269. https://doi.org/10.3897/zookeys.741.21971
Myriapoda threatened species geographic coordinates :
Figure 3 from: Karam-Gemael M, Izzo T, Chagas-Jr A (2018) Why be red listed? Threatened Myriapoda species in Brazil with implications for their conservation. In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 255-269. https://doi.org/10.3897/zookeys.741.21971
Figure 3 Distribution of the Brazilian Myriapoda threatened species. The color of the legend represents the IUCN threatened category: red (Critically endangered – CR), orange (Endangered – EN), and yellow (Vulnerable – VU). Species in blue are only known from subterranean habitats. Species with an asterisk (*) occur inside PAs.
Figure 2 from: Karam-Gemael M, Izzo T, Chagas-Jr A (2018) Why be red listed? Threatened Myriapoda species in Brazil with implications for their conservation. In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 255-269. https://doi.org/10.3897/zookeys.741.21971
Figure 2 Myriapoda species assessement by the current Brazilian Red List. Myriapoda threatened species according to the 2014 Brazilian Red List, which follows IUCN classification categories (CR = Critically endangered, EN = Endangered, VU = Vulnerable, NT = Near threatened, LC = Least concern, DD = Data deficient). Dashed red line indicates threatened categories.
Figure 1 from: Karam-Gemael M, Izzo T, Chagas-Jr A (2018) Why be red listed? Threatened Myriapoda species in Brazil with implications for their conservation. In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 255-269. https://doi.org/10.3897/zookeys.741.21971
Figure 1 Myriapoda in the IUCN and Brazilian red lists. Timeline of Myriapoda species included in the IUCN Red Lists of Threatened Species (above the red line), and in the Brazilian Red Lists of Threatened Species (below the red line), highlighting the first myriapods listed and the current number of species listed.
Figure 2 from: Correa C, Zepeda P, Lagos N, Salinas H, Palma RE, Vásquez D (2018) New populations of two threatened species of Alsodes (Anura, Alsodidae) reveal the scarce biogeographic knowledge of the genus in the Andes of central Chile. Zoosystematics and Evolution 94(2): 349-358. https://doi.org/10.3897/zse.94.25189
Figure 2 Adult males of Alsodes from the new discovered localities. In parentheses the specific identification according to the phylogenetic analysis (Fig. 3), the snout-vent length (SVL) and code of the respective buccal mucosa sample are indicated. A. Vegas de Cisternas (A. hugoi, SVL = 68.3 mm, VC1m). B. Cajón de Plaza (undetermined, SVL = 54.8 mm, CP5m). C. Vegas de Andrade (A. hugoi, SVL = 57.2 mm, VA1m). D. Vegas de Miranda (A. hugoi, SVL = 56.3 mm, VM6m). E. Cajón Lagunitas (site 3) (A. hugoi, SVL = 71.7 mm, CLP3-5m). F. Lo Aguirre Chico (A. pehuenche, SVL = 52.0 mm, AgCh4m). Some populations are characterized by well-developed interdigital webbing in the hind feet (shown in the insets).
Figure 1 from: Correa C, Zepeda P, Lagos N, Salinas H, Palma RE, Vásquez D (2018) New populations of two threatened species of Alsodes (Anura, Alsodidae) reveal the scarce biogeographic knowledge of the genus in the Andes of central Chile. Zoosystematics and Evolution 94(2): 349-358. https://doi.org/10.3897/zse.94.25189
Figure 1 New and literature records of Alsodes from the Andes Range between 34°50' and 38°05'S. Yellow circles represent the new localities reported in this study; squares represent type localities. A. Andean localities of Alsodes of the literature between 34°50' and 38°05'S: the southernmost localities of A. montanus and A. tumultuosus, the type locality of A. hugoi, localities of A. pehuenche (within red box B, see map B) and the type locality of A. vittatus. There is a record of a putative new species related to A. nodosus in Pemehue (Alsodes sp. 1 of Blotto et al. 2013; not included in the map), presumably the same type locality of A. vittatus. Red boxes correspond to the three explored areas described in this study (maps B, C and D). B. Area explored during the first field campaign (Paso Pehuenche, Laguna del Maule and surroundings). All colored symbols correspond to localities of A. pehuenche: yellow circles correspond to new records; green circles and the square are all previously known localities of the species. The white circle is the place where no amphibian was found. C. Area and sites explored during the third field campaign (tributaries of the Guaiquivilo River). D. Area and sites explored during the second field campaign (surroundings of Laguna El Dial). See details of the localities and the populations discovered in Table 1. Orange lines represent the boundary between Chile and Argentina; thinner yellow lines indicate the boundaries of the administrative regions of Chile.
Figure 3 from: Correa C, Zepeda P, Lagos N, Salinas H, Palma RE, Vásquez D (2018) New populations of two threatened species of Alsodes (Anura, Alsodidae) reveal the scarce biogeographic knowledge of the genus in the Andes of central Chile. Zoosystematics and Evolution 94(2): 349-358. https://doi.org/10.3897/zse.94.25189
Figure 3 Bayesian consensus tree (50% majority-rule) showing the relationships of the new Andean populations of Alsodes. Representatives of the new populations are labeled in green (related to A. pehuenche) and red (related to A. hugoi) (see details of the new localities in Table 1). Note that specimens from Cajón de Plaza are distributed in both the red and green clades. Reference sequences of the type localities of A. pehuenche and A. hugoi are in bold. Numbers next to the nodes correspond to posterior probabilities (only values ≥ 0.95 of the more internal nodes are shown). The scale bar in the lower left corner represents the expected substitutions per site along the branches.
Figure 3 from: Gâteblé G, Munzinger J (2018) Novitates neocaledonicae X: A very rare and threatened new microendemic species of Acropogon (Malvaceae, Sterculioideae) from New Caledonia. PhytoKeys 110: 1-8. https://doi.org/10.3897/phytokeys.110.27599
Figure 3 Acropogonhorarius Gâteblé & Munzinger sp. nov. A overview of a single mature shrub in habitat B juvenile plant C leaf D flowering branch E inflorescence F male flower G female flower H follicles. Photographs by G. Gâteblé (AGâteblé et al. 803BGâteblé et al. 804C–HGâteblé et al. 806).
Figure 1 from: Gâteblé G, Munzinger J (2018) Novitates neocaledonicae X: A very rare and threatened new microendemic species of Acropogon (Malvaceae, Sterculioideae) from New Caledonia. PhytoKeys 110: 1-8. https://doi.org/10.3897/phytokeys.110.27599
Figure 1 Distribution of Acropogonhorarius Gâteblé & Munzinger sp. nov. mapped on the geological (A) and soil (B) GIS layers of the Petchécara Pass. Insert A, geology from Gouvernement de la Nouvelle-Calédonie (2018): Λ1, serpentinites; Δ, amphibolites; B1, undifferentiated poly-metamorphic substrate; βP1, undifferentiated basalts and dolerites; Fyz, recent and extant alluvial; Li, listwanites. Insert B, soils from Fritsch (2012): 3d, haplic cambisol combined with lithic leptosol on peridotites; 3e, ferralic cambisol combined with haplic ferralsol on volcano-sedimentary and metamorphic rocks; 5b, posic ferralsol on peridotites.
Figure 2 from: Gâteblé G, Munzinger J (2018) Novitates neocaledonicae X: A very rare and threatened new microendemic species of Acropogon (Malvaceae, Sterculioideae) from New Caledonia. PhytoKeys 110: 1-8. https://doi.org/10.3897/phytokeys.110.27599
Figure 2 Acropogonhorarius Gâteblé & Munzinger sp. nov. A flowering branch B inflorescence and a zoom on stellate trichomes of the flower tube C female flower D male flower E infructescence F detail of erect stellate trichomes on the follicle's surface G detail of an open follicle H close-up of the abaxial leaf reticulum. Drawings by Laurence Ramon (A–H Gâteblé et al. 806).
Fig. 3. Nhambikuara mima comb. nov. A in Before it is too late: description of a new genus and species of butterfly from a highly threatened Brazilian biome
Fig. 3. Nhambikuara mima comb. nov. A – male, dorsal (DZ 35.877); B – male, ventral; C – female, dorsal (DZ 34.823); D – female, ventral.
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.