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81 results for “threatened genus”
Figure 3 in Reproductive biology of direct developing and threatened frog Adelophryne maranguapensis (Anura, Eleutherodactylidae) reveals a cryptic reproductive mode for anurans and the first record of parental care for the genus
Figure 3. Female Adelophryne maranguapensis showing parental care activity (clutch 13, Table 1).
Figure 1 in Reproductive biology of direct developing and threatened frog Adelophryne maranguapensis (Anura, Eleutherodactylidae) reveals a cryptic reproductive mode for anurans and the first record of parental care for the genus
Figure 1. Fieldwork areas. Riacho Beija-flor (a) and Pico da Rajada (b).
Fig. 1 in Hornschuchia (Annonaceae), an endemic and threatened genus from the Brazilian Atlantic Forest
Fig. 1. Geographical distribution of Hornschuchia alba (A.St.-Hil.) R.E.Fr. and H. bryotrophe Nees. Abbreviations: BA = Bahia; ES = Espírito Santo; MG = Minas Gerais; PE = Pernambuco; RJ = Rio de Janeiro.
Figure 6 from: de Lange PJ, Smissen RD, Rolfe JR, Ogle CC (2016) Systematics of Simplicia Kirk (Poaceae, Agrostidinae) – an endemic, threatened New Zealand grass genus. PhytoKeys 75: 119-144. https://doi.org/10.3897/phytokeys.75.10328
Figure 6 - Simplicia laxa. A habitat, Emerald Stream, McCraes, North Otago, South Island, New Zealand (image D.A. Houston) B growth habit and inflorescence C culm, leaf base, sheath and ligule D spikelet showing reduced glumes and lemma. (Photo credit images C and D: K. Ford, Allan Herbarium, Landcare Research Manaaki Whenua)
Figure 2 from: de Lange PJ, Smissen RD, Rolfe JR, Ogle CC (2016) Systematics of Simplicia Kirk (Poaceae, Agrostidinae) – an endemic, threatened New Zealand grass genus. PhytoKeys 75: 119-144. https://doi.org/10.3897/phytokeys.75.10328
Figure 2 - Selected most parsimonious tree for nrDNA sequence data. Numbers above branches are bootstrap percentages. Diagonal lines indicate that the branches leading to the outgroup Nicoraepoa and Catabrosia sequences are not shown to scale.
Figure 5 from: de Lange PJ, Smissen RD, Rolfe JR, Ogle CC (2016) Systematics of Simplicia Kirk (Poaceae, Agrostidinae) – an endemic, threatened New Zealand grass genus. PhytoKeys 75: 119-144. https://doi.org/10.3897/phytokeys.75.10328
Figure 5 - Simplicia buchananii. A habitat, Kahurangi National Park, North West Nelson, South Island, New Zealand B growth habit and inflorescence C culm, leaf base, sheath and ligule D spikelet showing reduced glumes and lemma (images: J.R. Rolfe).
Figure 8 from: de Lange PJ, Smissen RD, Rolfe JR, Ogle CC (2016) Systematics of Simplicia Kirk (Poaceae, Agrostidinae) – an endemic, threatened New Zealand grass genus. PhytoKeys 75: 119-144. https://doi.org/10.3897/phytokeys.75.10328
Figure 8 - Simplicia felix. A habitat, Te Kanuka Farm Station, Upper Kaumingi Stream east Wairarapa, North Island, New Zealand B growth habit and inflorescence C culm, leaf base, sheath and ligule D spikelet showing reduced glumes and lemma (images: J.R. Rolfe)
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.
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.
Fig. 1 in Before it is too late: description of a new genus and species of butterfly from a highly threatened Brazilian biome
Fig. 1. Nhambikuara cerradensis gen. et sp. nov. A – holotype male, dorsal; B – holotype male, ventral; C – allotype female, dorsal; D – allotype female, ventral.
Fig. 7 in Before it is too late: description of a new genus and species of butterfly from a highly threatened Brazilian biome
Fig. 7. Maximum likelihood consensus tree showing the phylogenetic relationships among species of Nhambikuara gen. nov. and exemplar species of Splendeuptychia. Numbers above branches are bootstrap values.
Linked collectors and determiners for: A Taxonomic Revision of Arapatiella (Fabaceae: Caesalpinioideae): An Endemic and Threatened Genus from the Brazilian Coast.
Natural history specimen data linked to collectors and determiners held within, "A Taxonomic Revision of Arapatiella (Fabaceae: Caesalpinioideae): An Endemic and Threatened Genus from the Brazilian Coast". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/3fef6e47-aeee-4ac6-bf20-ce768d931d03">https://bionomia.net/dataset/3fef6e47-aeee-4ac6-bf20-ce768d931d03</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/3fef6e47-aeee-4ac6-bf20-ce768d931d03">https://gbif.org/dataset/3fef6e47-aeee-4ac6-bf20-ce768d931d03</a>. Formatted as a Frictionless Data package.
Figure 3 from: de Lange PJ, Smissen RD, Rolfe JR, Ogle CC (2016) Systematics of Simplicia Kirk (Poaceae, Agrostidinae) – an endemic, threatened New Zealand grass genus. PhytoKeys 75: 119-144. https://doi.org/10.3897/phytokeys.75.10328
Figure 3 - NeighborNet graph for AFLP data with all automatically scored polymorphisms.
Figure 4 from: de Lange PJ, Smissen RD, Rolfe JR, Ogle CC (2016) Systematics of Simplicia Kirk (Poaceae, Agrostidinae) – an endemic, threatened New Zealand grass genus. PhytoKeys 75: 119-144. https://doi.org/10.3897/phytokeys.75.10328
Figure 4 - NeighborNet graph for reduced AFLP data with reproduced polymorphisms only.
Figure 1 from: de Lange PJ, Smissen RD, Rolfe JR, Ogle CC (2016) Systematics of Simplicia Kirk (Poaceae, Agrostidinae) – an endemic, threatened New Zealand grass genus. PhytoKeys 75: 119-144. https://doi.org/10.3897/phytokeys.75.10328
Figure 1 - Distribution of Simplicia species and showing locations discussed in text.
Figure 7 from: de Lange PJ, Smissen RD, Rolfe JR, Ogle CC (2016) Systematics of Simplicia Kirk (Poaceae, Agrostidinae) – an endemic, threatened New Zealand grass genus. PhytoKeys 75: 119-144. https://doi.org/10.3897/phytokeys.75.10328
Figure 7 - Holotype of Simplicia felix de Lange, J.R.Rolfe, Smissen & Ogle.
FIG. 1 in Cladistic, phenetic and biogeographical analysis of the ¯ightless dung beetle genus, Gyronotus van Lansberge (Scarabaeidae: Scarabaeinae), in threatened eastern Afrotropical forests
FIG. 1. Geographical distribution of Gyronotus species from east to southern Africa (T, Tanzania; M, Malawi; SA, South Africa) (S, Swahili centre of endemism; SM, Swahili-M aputaland transition zone (Burgess et al., 1998); Ma, M aputaland centre of endemism; P, Pondoland centre of endemism which occupies a narrow coastal zone (van R ensburg et al., 1999 )).
FIG. 4 in Cladistic, phenetic and biogeographical analysis of the ¯ightless dung beetle genus, Gyronotus van Lansberge (Scarabaeidae: Scarabaeinae), in threatened eastern Afrotropical forests
FIG. 4. Distal and ventral views of canthonine aedeagi showing diOEerences in paramere morphology between: (A) Anachalcos procerus Gerstaecker (distal), (B) Canthodimorph a lawrencei Davis, Scholtz and Harrison (ventral), (C) east African Gyronotus van Lansberge (ventral) (C1, G. Wmetarius K olbe; C2, G. mulanjensis D avis, Scholtz and Harrison; C3, G. dispar (Felsche)) and (D) South African Gyronotus (ventral) (D 1, G. carinatus Felsche; D 2, G. glabrosus Scholtz and Howden; D 3, G. pumilus (Boheman)). Scale bars 5 1 mm.
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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)
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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.