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.
1,118
datasets available to search
ShareScore release 0.9.0
Dataset results
1,118 results for “subterranean biology”
Figure 2 from: Dörge D, Zaenker S, Klussmann-Kolb A, Weigand A (2014) Traversing worlds - Dispersal potential and ecological classification of Speolepta leptogaster (Winnertz, 1863) (Diptera, Mycetophilidae). Subterranean Biology 13: 1-16. https://doi.org/10.3897/subtbiol.13.6460
Figure 2 - Spatial pattern of haplotypes of Speolepta leptogaster in Hesse. The haplotype (H) distribution of Speolepta leptogaster within Hesse (A) with a comparison group in Poland (B) is depicted as a circle for every underground locality with colored sections for the different haplotypes. To be depicted in a reasonable manner, multiple localities were reduced to one circle if they were situated nearby (up to 4 km) and had the same color.
Figure 4 from: Espinasa L, D. Bartolo N, E. Newkirk C (2014) DNA sequences of troglobitic nicoletiid insects support Sierra de El Abra and the Sierra de Guatemala as a single biogeographical area: Implications for Astyanax. Subterranean Biology 13: 35-44. https://doi.org/10.3897/subtbiol.13.7256
Figure 4 - The Boquillas River has changed its course throughout time. The Boquillas River currently separates the karstic areas of Sierra de Guatemala from the Sierra the El Abra. In the upper part of the figure, the Boquillas River is seen crossing the sierras through the Servilleta canyon. On the bottom part of the figure, a fossil canyon indicates the river's ancient course. Caves that in the past connected the Sierra de El Abra in the south to the Sierra de Guatemala in the north were only recently geologically truncated by the erosion of the new river course. Limestone is restricted to the green forested hills.
Figure 3 from: Espinasa L, D. Bartolo N, E. Newkirk C (2014) DNA sequences of troglobitic nicoletiid insects support Sierra de El Abra and the Sierra de Guatemala as a single biogeographical area: Implications for Astyanax. Subterranean Biology 13: 35-44. https://doi.org/10.3897/subtbiol.13.7256
Figure 3 - Base pair differences versus estimates of divergence in nicoletiids. Base pair differences in the 16S rRNA fragment is plotted against estimates of divergence times millions of years ago (Mya). Molecular clock calibrating points were extracted from: a populations of Anelpistina musticensis that got separated into different islands when the sea level rose after glacial times 12,000 years ago (Espinasa et al. 2011) b and c species of Prosthecina and d species of Anelpistina from Baja California that got separated from the mainland species when the Gulf of Cortes formed 5 mya (Espinasa et al. 2009) e time when nicoletiids arose from a common ancestor with Lepismatids 302 mya (Regier et al. 2010), and f time when insects arose from a common ancestor with anostraca in the Silurian-Ordovician boundary 427 mya (Gaunt and Miles 2002). The lower arrow indicates the 11–12 bp differences between the Sierra de Guatemala and the Sierra de El Abra Anelpistina populations. Such sequence difference is consistent with a common origin very recently, less than 12,000 years ago, and therefore after the environmental disturbances of the ice age.
Figure 4 from: Halse S, Pearson G (2014) Troglofauna in the vadose zone: comparison of scraping and trapping results and sampling adequacy. Subterranean Biology 13: 17-34. https://doi.org/10.3897/subtbiol.13.6991
Figure 4 - Taxonomic composition of troglofauna in the Pilbara and Yilgarn. Orders in legend are shown clockwise from the top of the pie chart.
Figure 2 from: Espinasa L, D. Bartolo N, E. Newkirk C (2014) DNA sequences of troglobitic nicoletiid insects support Sierra de El Abra and the Sierra de Guatemala as a single biogeographical area: Implications for Astyanax. Subterranean Biology 13: 35-44. https://doi.org/10.3897/subtbiol.13.7256
Figure 2 - Anelpistina quinterensis is one of the most troglomorphic described species of nicoletiids. This relatively large eyeless insect is albino and has extremely elongated appendages. Its habitat is restricted to very humid portions of the caves such as mud banks. It is doubtful that it can survive in an epigean environment. Its habitat probably reflects connectivity within a karstic area throughout geologic times and during the evolutionary history of the species.
Figures 10-11 from: Zeppelini D, Silva D, Palacios Vargas J (2014) A new species of Troglobius (Collembola, Paronellidae, Cyphoderinae) from a Brazilian iron cave. Subterranean Biology 14: 1-13. https://doi.org/10.3897/subtbiol.14.7355
Figures 10-11 - 10 Ventral tube chaetotaxy, lateral view, Troglobius ferroicus sp. n. 11 Distal end of dens and mucro, Troglobius ferroicus sp. n.
Figure 1 from: Espinasa L, D. Bartolo N, E. Newkirk C (2014) DNA sequences of troglobitic nicoletiid insects support Sierra de El Abra and the Sierra de Guatemala as a single biogeographical area: Implications for Astyanax. Subterranean Biology 13: 35-44. https://doi.org/10.3897/subtbiol.13.7256
Figure 1 - The Cañon de la Servilleta of the River Boquillas separates the contiguous Sierra de Guatemala, to the north, from the Sierra de El Abra, in the south. Limestone is restricted to the green forested hills. This study tested if this 100 m high, 100 m wide canyon was an effective biological barrier that prevented underground migration of troglobites between the two karstic areas.
Figure 5 from: Latella L, Di Russo C, Rampini M, Cobolli M (2014) Measurements of the diet in two species of Troglophilus Krauss, 1879 cave crickets from Italian subterranean habitats (Orthoptera, Rhaphidophoridae). Subterranean Biology 13: 45-54. https://doi.org/10.3897/subtbiol.13.6719
Figure 5 - Comparison of the autumnal diet between female and male sub-samples of Troglophilus andreinii. Grey: green vegetables; light grey: fibres; black: arthropod remains.
Figure 4 from: Latella L, Di Russo C, Rampini M, Cobolli M (2014) Measurements of the diet in two species of Troglophilus Krauss, 1879 cave crickets from Italian subterranean habitats (Orthoptera, Rhaphidophoridae). Subterranean Biology 13: 45-54. https://doi.org/10.3897/subtbiol.13.6719
Figure 4 - Overlap analysis of food resource exploitation conducted in individuals of different age (young instars, nymphs and adults). The dendrograms were performed using euclidean distances based on the Morisita-Horn index matrices. (a: Troglophilus cavicola, b: Troglophilus andreinii).
Figure 3 from: Latella L, Di Russo C, Rampini M, Cobolli M (2014) Measurements of the diet in two species of Troglophilus Krauss, 1879 cave crickets from Italian subterranean habitats (Orthoptera, Rhaphidophoridae). Subterranean Biology 13: 45-54. https://doi.org/10.3897/subtbiol.13.6719
Figure 3 - Comparison of the diet among age sub-samples (Young instars, Nymphs and Adults) of Troglophilus cavicola and Troglophilus andreinii. Grey: green vegetables; light grey: fibres; black: arthropod remains.
Figure 2 from: Mock A, Hudec I (2014) Niphargus plurispinosus sp. n. (Crustacea, Amphipoda), a stygophile and hypotelminorheic representative from Central Europe. Subterranean Biology 13: 65-87. https://doi.org/10.3897/subtbiol.13.6531
Figure 2 - Niphargus plurispinosus sp. n.: 1 male, general view; 1a-1b dorso-later thorns; mdb - mandibula and details of mdb-a left incisor and lacina mobilis; mdb-b) two setae between bisserated thorns; mdb-c setae pattern on distal segment of mdb-palp; mdb-d, right incisor and lacina mobilis; mx-1 1st maxilla; mx-2 2nd maxilla; ula upper lip; vela ventral labium; mxp maxilliped: in inner segment os outer segment; ds distal segment of palp; epI-epIII epimeral plate I-III; A-I 1st antenna; A-II antenna; hc head capsula, left lateral view; telson, dorsal view. Not scaled, except of the general view of the male.
Figure 2 from: Latella L, Di Russo C, Rampini M, Cobolli M (2014) Measurements of the diet in two species of Troglophilus Krauss, 1879 cave crickets from Italian subterranean habitats (Orthoptera, Rhaphidophoridae). Subterranean Biology 13: 45-54. https://doi.org/10.3897/subtbiol.13.6719
Figure 2 - Comparison of seasonal niche breadth in Troglophilus cavicola and Troglophilus andreinii populations
Figure 8 from: Mock A, Hudec I (2014) Niphargus plurispinosus sp. n. (Crustacea, Amphipoda), a stygophile and hypotelminorheic representative from Central Europe. Subterranean Biology 13: 65-87. https://doi.org/10.3897/subtbiol.13.6531
Figure 8 - Variability of telson setae of Niphargus plurispinosus sp. n.: A–E, H juveniles (males and females) F adult male G adult female I postreproductive male J postreproductive female K 3rd uropod of female (Photo: I. Hudec). Not scaled.
Figure 5 from: Mock A, Hudec I (2014) Niphargus plurispinosus sp. n. (Crustacea, Amphipoda), a stygophile and hypotelminorheic representative from Central Europe. Subterranean Biology 13: 65-87. https://doi.org/10.3897/subtbiol.13.6531
Figure 5 - Niphargus plurispinosus sp. n.: gpI 1st gnathopod; gpII 2nd gnathopod; ppIII–ppIV, ppVI–ppVII 3rd to 7th pereopods; ppV-b – ppVII-b bases of 5th to 7th pp; ppV-d – ppVII-d distal part of 5th to 7th pp; plp 2nd pleopod; upI and up II 1st and 2nd uropod; upIII-f 3rd uropod of female; upIII-m 3rd uropod of male; cxI-cxVII 1st to 7th coxal plate. Remarks: shadow colour was used to emphasise of important character. Not drawn to scale.
Figure 2 from: Rosa G, Penado A (2013) Rana iberica (Boulenger, 1879) goes underground: subterranean habitat usage and new insights on natural history. Subterranean Biology 11: 15-29. https://doi.org/10.3897/subtbiol.11.5170
Figure 2 - Polar coordinates representing the activity cycle and breeding period of Rana iberica in two different sites (inside the drainage gallery in Sazes and the whole area of Planalto Superior) in Serra da Estrela; Portugal. Dark brown areas: post-metamorphic phase; beige areas: larval phase; green areas: adults in breeding activity.
Figure 5 from: Moldovan O, Fejér A (2013) Population size and dispersal patterns for a Drimeotus (Coleoptera, Leiodidae, Leptodirini) cave population. Subterranean Biology 11: 31-44. https://doi.org/10.3897/subtbiol.11.4974
Figure 5 - Box-plot of the number of individuals of Drimeotus viehmanni, in the winter and the summer months, in the five stations (I–V) of Peştera cu Apă din Valea Leşului.
Figure 1 from: Rosa G, Penado A (2013) Rana iberica (Boulenger, 1879) goes underground: subterranean habitat usage and new insights on natural history. Subterranean Biology 11: 15-29. https://doi.org/10.3897/subtbiol.11.5170
Figure 1 - Serra da Estrela Natural Park and hypogean habitat used by individuals of Rana iberica: A entrance of the underground spring B Schistostega pennata covering walls and floor of the drainage gallery C horizontal tunnel of drainage gallery. Photo A by Madeira M, B by Rosa GM, C by Laurentino T.
Figure 4 from: Moldovan O, Fejér A (2013) Population size and dispersal patterns for a Drimeotus (Coleoptera, Leiodidae, Leptodirini) cave population. Subterranean Biology 11: 31-44. https://doi.org/10.3897/subtbiol.11.4974
Figure 4 - Monthly variation of the number of individuals of Drimeotus viehmanni in the five stations (I–V) of Peştera cu Apă din Valea Leşului.
Figure 2 from: Moldovan O, Fejér A (2013) Population size and dispersal patterns for a Drimeotus (Coleoptera, Leiodidae, Leptodirini) cave population. Subterranean Biology 11: 31-44. https://doi.org/10.3897/subtbiol.11.4974
Figure 2 - Box-plot of the air temperature, during winter and summer months, at the surface (S), the entrance (E) and the five stations (I-V) for Peştera cu Apă din Valea Leşului.
Figure 7 from: Moldovan O, Fejér A (2013) Population size and dispersal patterns for a Drimeotus (Coleoptera, Leiodidae, Leptodirini) cave population. Subterranean Biology 11: 31-44. https://doi.org/10.3897/subtbiol.11.4974
Figure 7 - The migration routes of Drimeotus viehmanni inside Peştera cu Apă din Valea Leşului: yellow = mark for individuals at station II, blue = mark for individuals at station III.
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.