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1,118 results for “subterranean biology”
Figure 10 from: Jantarit S, Deharveng L, Surakhamhaeng K (2021) Three new species of cave Troglopedetes (Collembola, Paronellidae, Troglopedetinae) from Thailand, with a key to the Thai species. Subterranean Biology 40: 129-174. https://doi.org/10.3897/subtbiol.40.73143
Figure 10 Troglopedetes takensis sp. nov., continued A distal part of tibiotarsus III and claw complex with pointed tenent hair B trochanteral organ C mucro D posterior side of ventral tube E lateral flap of ventral tube.
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 1 from: Jantarit S, Deharveng L, Surakhamhaeng K (2021) Three new species of cave Troglopedetes (Collembola, Paronellidae, Troglopedetinae) from Thailand, with a key to the Thai species. Subterranean Biology 40: 129-174. https://doi.org/10.3897/subtbiol.40.73143
Figure 1 Distribution of Troglopedetes in Thailand (green circles) with limestone terrains (red colour) of the country 1T. maffrei Deharveng & Gers, 1993 2T. longicornis Deharveng & Gers, 1993 3T. centralis Deharveng & Gers, 1993 4T. fredstonei Deharveng, 1988 5T. leclerci Deharveng, 1990 6T. microps Deharveng & Gers, 1993 7T. multispinosus Deharveng & Gers, 1993 8T. maungonensis Deharveng & Gers, 1993 9T. calvus Deharveng & Gers, 1993 10T. dispersus Deharveng & Gers, 1993 11T. convergens Deharveng & Gers, 1993 12T. paucisetosus Deharveng & Gers, 1993 13T. meridionalis Jantarit, Surakhamhaeng & Deharveng, 2020 14T. kae Jantarit, Surakhamhaeng & Deharveng, 2020 15T. spectabilis sp. nov. 16T. takensis sp. nov. 17T. rungsimae sp. nov. (blue circles) and undescribed species of Troglopedetes found in Thailand (black circles). Regional boundary indicated by grey line; province capitals as small dark dots; scale 1:250,000.
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 8 from: Jantarit S, Deharveng L, Surakhamhaeng K (2021) Three new species of cave Troglopedetes (Collembola, Paronellidae, Troglopedetinae) from Thailand, with a key to the Thai species. Subterranean Biology 40: 129-174. https://doi.org/10.3897/subtbiol.40.73143
Figure 8 Troglopedetes takensis sp. nov. A head chaetotaxy B papilla E of labial palp C outer maxillary lobe D antenna E labrum F clypeus G labial basis and ventral chaetotaxy of head, right side.
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.
Figure 6 from: Farikou PO, Christophe P, Bertrand SNP, Hubert ZTS (2021) Distribution of Stenasellidae in Africa and description of a new species of Metastenasellus from Cameroonian groundwaters. Subterranean Biology 40: 175-194. https://doi.org/10.3897/subtbiol.40.76301
Figure 6 Pleopods 2 of males Metastenasellus as drawn in original descriptions (A) M. leleupi (scale 1) (B) M. camerounensis (scale 1) (C) M. dartivellei (scale 2) (D) M. powelli (scale 3) (E) M. congolensis (scale 1) (F) M. boutini (scale 2) (G) M. leysi (scale 3) (H) M. wikkiensis (scale 2) (I) M. tarrissei (scale 3).
Figure 5 from: Farikou PO, Christophe P, Bertrand SNP, Hubert ZTS (2021) Distribution of Stenasellidae in Africa and description of a new species of Metastenasellus from Cameroonian groundwaters. Subterranean Biology 40: 175-194. https://doi.org/10.3897/subtbiol.40.76301
Figure 5 Neighbor-joining tree of the identified COI gene haplotypes. The evolutionary distances were computed using the Kimura two-parameter (K2P) model. Numbers between brackets in front of the nodes indicate bootstrap support (1,000 replicates). Boxes on the right indicate the best partition of species using ASAP, ABGD, mPTP and GMYC delimitation methods.
Figure 3 from: Farikou PO, Christophe P, Bertrand SNP, Hubert ZTS (2021) Distribution of Stenasellidae in Africa and description of a new species of Metastenasellus from Cameroonian groundwaters. Subterranean Biology 40: 175-194. https://doi.org/10.3897/subtbiol.40.76301
Figure 3 Metastenasellus boutini sp. nov., ((A–C) ♂ holotype 9.8 mm) (A), pereopod 5 (B) pereopod 6 (C) pereopod 7.
Figure 2 from: Farikou PO, Christophe P, Bertrand SNP, Hubert ZTS (2021) Distribution of Stenasellidae in Africa and description of a new species of Metastenasellus from Cameroonian groundwaters. Subterranean Biology 40: 175-194. https://doi.org/10.3897/subtbiol.40.76301
Figure 2 Metastenasellus boutini sp. nov., ((A–D) ♂ holotype 9.8 mm) (A) pereopod 1 (B) pereopod 2 (C) pereopod 3 (D) pereopod 4.
Figure 7 from: Farikou PO, Christophe P, Bertrand SNP, Hubert ZTS (2021) Distribution of Stenasellidae in Africa and description of a new species of Metastenasellus from Cameroonian groundwaters. Subterranean Biology 40: 175-194. https://doi.org/10.3897/subtbiol.40.76301
Figure 7 Distribution map of Stenasellidae in Africa: Acanthastenasellus (A. forficuloides); Johanella (J. purpurea); Magniezia (Ma1: M. africana, Ma2: M. gardei, Ma3: M. guinensis, Ma4: M. laticarpa, Ma5: M. studiosorum); Metastenasellus (Me1: M. boutini, Me2: M. camerounensis, Me3: M. congolensis, Me4: M. dartvellei, Me5: M. leleupi, Me6: M. leysi, Me7: M. powelli, Me8: M. tarrissei, Me9: M. wikkiensis, Me10: Metastenasellus sp1, Me11: Metastenasellus sp2, Me12: Metastenasellus sp3, Me13: Metastenasellus sp. 4, Me14: Metastenasellus sp5); Parastenasellus (P. chappuisi); Stenasellus (St1: S. agiuranicus, St2: S. costai, St3: S. kenyensis, St4: S. migiurtinicus, St5: S. pardii, St6: S. ruffoi, St7: S. simonsi).
Figure 4 from: Farikou PO, Christophe P, Bertrand SNP, Hubert ZTS (2021) Distribution of Stenasellidae in Africa and description of a new species of Metastenasellus from Cameroonian groundwaters. Subterranean Biology 40: 175-194. https://doi.org/10.3897/subtbiol.40.76301
Figure 4 Metastenasellus boutini sp. nov., ((A–B, D–G) ♂ holotype 9.8 mm (C) ♀ paratype 8 mm) (A) pleopod 1 (scale 1) (B) pleopod 2 (scale 1) (C) ♀ pleopod 2 (scale 1) (D) pleopod 3 (scale 2) (E) pleopod 4 (scale 1) (F) pleopod 5 (scale 1) (G), uropod (scale 2).
Figure 1 from: Farikou PO, Christophe P, Bertrand SNP, Hubert ZTS (2021) Distribution of Stenasellidae in Africa and description of a new species of Metastenasellus from Cameroonian groundwaters. Subterranean Biology 40: 175-194. https://doi.org/10.3897/subtbiol.40.76301
Figure 1 Metastenasellus boutini sp. nov., ((A–H), ♂ holotype 9.8 mm) (A) habitus (scale 1) (B) antenna 1 (scale 2) (C) antenna 2 (scale 3) (D) left mandible (scale 4) (E) right mandible (scale 4) (F) maxilla 1 (scale 4) (G) maxilla 2 (scale 4) (H) maxilliped (scale 4).
Supplementary material 1 from: Nilsai A, Detcharoen M, Godeiro NN, Jantarit S (2021) Four new species of troglomorphic Coecobrya Yosii, 1956 (Collembola, Entomobryidae) from Thailand based on morphological and molecular evidence, with an updated key of Thai troglomorphic species. Subterranean Biology 41: 1-42. https://doi.org/10.3897/subtbiol.41.76926
Maximum likelihood phylogenetic tree (ML)
Supplementary material 2 from: Nilsai A, Detcharoen M, Godeiro NN, Jantarit S (2021) Four new species of troglomorphic Coecobrya Yosii, 1956 (Collembola, Entomobryidae) from Thailand based on morphological and molecular evidence, with an updated key of Thai troglomorphic species. Subterranean Biology 41: 1-42. https://doi.org/10.3897/subtbiol.41.76926
Table 1–3. Primers, genetic distance and Genbank accession numbers
Figure 9 from: Nilsai A, Detcharoen M, Godeiro NN, Jantarit S (2021) Four new species of troglomorphic Coecobrya Yosii, 1956 (Collembola, Entomobryidae) from Thailand based on morphological and molecular evidence, with an updated key of Thai troglomorphic species. Subterranean Biology 41: 1-42. https://doi.org/10.3897/subtbiol.41.76926
Figure 9 Coecobrya ellisi sp. nov., continued A Chaetae of labial basis and ventral chaetotaxy of head B Chaetae of labial basis C Posterior side of ventral tube and Lateral flap D Dorsal cephalic chaetotaxy E Manubrium plaque F Mucro G Distal part of manubrium ventrally.
Figure 6 from: Nilsai A, Detcharoen M, Godeiro NN, Jantarit S (2021) Four new species of troglomorphic Coecobrya Yosii, 1956 (Collembola, Entomobryidae) from Thailand based on morphological and molecular evidence, with an updated key of Thai troglomorphic species. Subterranean Biology 41: 1-42. https://doi.org/10.3897/subtbiol.41.76926
Figure 6 Coecobrya troglobia sp. nov., continued A Posterior side of ventral tube B Anterior side of ventral tube C Posterior side of ventral tube D Distal part of manubrium ventrally E Trochanteral organ F Mucro G Distal part of tita III and claw complex H Mandibles I Dorsal cephalic chaetotaxy.
Figure 8 from: Nilsai A, Detcharoen M, Godeiro NN, Jantarit S (2021) Four new species of troglomorphic Coecobrya Yosii, 1956 (Collembola, Entomobryidae) from Thailand based on morphological and molecular evidence, with an updated key of Thai troglomorphic species. Subterranean Biology 41: 1-42. https://doi.org/10.3897/subtbiol.41.76926
Figure 8 Coecobrya ellisi sp. nov. A Prelabral and labral chaetae B Labial palp C Ventro-distal complex of labrum D Subapical organ of Ant. IVE Mandibles F Outer maxillary lobe G Clypeal chaetae H Anterior side of ventral tube and Lateral flap I Lateral flap J Distal part of tita III and claw complex K Trochanteral organ.
Figure 7 from: Nilsai A, Detcharoen M, Godeiro NN, Jantarit S (2021) Four new species of troglomorphic Coecobrya Yosii, 1956 (Collembola, Entomobryidae) from Thailand based on morphological and molecular evidence, with an updated key of Thai troglomorphic species. Subterranean Biology 41: 1-42. https://doi.org/10.3897/subtbiol.41.76926
Figure 7 Coecobrya troglobia sp. nov., continued A Chaetotaxy of dorsal Th. II– III B dorsal Abd. I– III C Chaetotaxy of dorsal Abd. IVD Chaetotaxy of dorsal Abd. V.
Figure 4 from: Nilsai A, Detcharoen M, Godeiro NN, Jantarit S (2021) Four new species of troglomorphic Coecobrya Yosii, 1956 (Collembola, Entomobryidae) from Thailand based on morphological and molecular evidence, with an updated key of Thai troglomorphic species. Subterranean Biology 41: 1-42. https://doi.org/10.3897/subtbiol.41.76926
Figure 4 Coecobrya whitteni sp. nov., continued A Chaetotaxy of dorsal Th. II– III B Chaetotaxy of dorsal Abd. I– III C Chaetotaxy of dorsal Abd. IVD Chaetotaxy of dorsal Abd. V.
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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
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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.