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1,118 results for “subterranean biology”
Figure 4 from: Conde-Vela VM (2019) Sinkhole and brackish water nereidid polychaetes: Revision of Stenoninereis Wesenberg-Lund, 1958 (Annelida). Subterranean Biology 30: 95-115. https://doi.org/10.3897/subtbiol.30.36273
Figure 4 Stenoninereislackeyi (Hartman, 1958) comb. n. A–J paratype (AHF-POLY-806) A whole specimen, dorsal view B anterior end, dorsal view C posterior end, dorsal view D notopodial sesquigomph spiniger, chaetiger 27 E supra-acicular sesquigomph spinigers, chaetiger 27 F sub-acicular heterogomph spiniger, chaetiger 27 G sub-acicular heterogomph falcigers (uppermost one at the left), chaetiger 27 H chaetiger 7, right parapodium, anterior view I chaetiger 19, right parapodium, anterior view J chaetiger 26, right parapodium, anterior view. Scale bars: 1 mm (A); 0.25 mm (B–C); 10 µm (D–G) 0.1 mm (H–J).
Figure 3 from: Conde-Vela VM (2019) Sinkhole and brackish water nereidid polychaetes: Revision of Stenoninereis Wesenberg-Lund, 1958 (Annelida). Subterranean Biology 30: 95-115. https://doi.org/10.3897/subtbiol.30.36273
Figure 3 Stenoninereismartini Wesenberg-Lund, 1958 A–J non-type specimens (USNM 61623) A chaetiger 2, right parapodium, anterior view B chaetiger 9, right parapodium, anterior view C chaetiger 21, right parapodium, anterior view D chaetiger 27, right parapodium, anterior view E chaetiger 28, left parapodium, anterior view F notopodial sesquigomph spinigers, chaetiger 28 G supra-acicular sesquigomph spinigers, chaetiger 28 H sub-acicular heterogomph spiniger, chaetiger 28 I sub-acicular heterogomph spiniger, chaetiger 28 J left jaw, dorsal view. Scale bars: 50 µm (A, D); 0.1 mm (B–C); 10 µm (F–I); 50 µm (J).
Figure 6 from: Conde-Vela VM (2019) Sinkhole and brackish water nereidid polychaetes: Revision of Stenoninereis Wesenberg-Lund, 1958 (Annelida). Subterranean Biology 30: 95-115. https://doi.org/10.3897/subtbiol.30.36273
Figure 6 Stenoninereiselisae sp. nov. A–M Syntypes (USNM 55366) A whole specimen, dorsal view B whole specimens, dorsal view C anterior end, dorsal view D Posterior end, dorsal view E chaetiger 6, right parapodium, anterior view F chaetiger 16, right parapodium, anterior view G chaetiger 18, right parapodium, anterior view H chaetiger 24, right parapodium, anterior view I subacicular heterogomph spinigers, chaetiger 18 J–L subacicular heterogomph falcigers, chaetiger 18 M notopodial homogomph spiniger, chaetiger 49. Scale bars: 0.5 mm (A–B); 0.25 mm (C); 0.2 mm (E–H); 10 µm (I–L); 30 µm (M).
Figure 1 from: Bercea S, Năstase-Bucur R, Moldovan OT, Kenesz M, Constantin S (2019) Yearly microbial cycle of human exposed surfaces in show caves. Subterranean Biology 31: 1-14. https://doi.org/10.3897/subtbiol.31.34490
Figure 1 Monitoring sites; Location of the studied caves in Romania with the cave maps and monitoring sites in Ursilor (A modified after Rusu and Racoviţă 1981) and Muierilor (B modified after map by Grigore, Fofirică, Dăscălescu and Iliescu, unpublished).
Figure 2 from: Benítez S, Illife TM, Quiroz-Martínez B, Alvarez F (2019) How is the anchialine fauna distributed within a cave? A study of the Ox Bel Ha System, Yucatan Peninsula, Mexico. Subterranean Biology 31: 15-28. https://doi.org/10.3897/subtbiol.31.34347
Figure 2 Ecological parameters of the anchialine fauna in the Ox Bel Ha anchialine cave system along a transect A mean ± one standard error of the abundance B mean ± one standard error of the species richness C Shannon's diversity index. The sites are: T, Tábano; O, Odyssey; M, Muknal; B, Bang.
Figure 1 from: Benítez S, Illife TM, Quiroz-Martínez B, Alvarez F (2019) How is the anchialine fauna distributed within a cave? A study of the Ox Bel Ha System, Yucatan Peninsula, Mexico. Subterranean Biology 31: 15-28. https://doi.org/10.3897/subtbiol.31.34347
Figure 1 Map of the Ox Bel Ha anchialine cave system near the town of Tulum. Quintana Roo, Mexico. The four cenotes used to access the cave were: Tábano, Odyssey, Muknal and Bang.
Figure 3 from: Bercea S, Năstase-Bucur R, Moldovan OT, Kenesz M, Constantin S (2019) Yearly microbial cycle of human exposed surfaces in show caves. Subterranean Biology 31: 1-14. https://doi.org/10.3897/subtbiol.31.34490
Figure 3 Distribution of culturable bacterial and fungal abundances on the Ursusspelaeus skeletons on display from 2015 to 2016 in Ursilor (A) and Muierilor (B). TB, total aerobic bacteria; YM, yeasts and moulds; E.coli, Escherichiacoli.
Figure 4 from: Benítez S, Illife TM, Quiroz-Martínez B, Alvarez F (2019) How is the anchialine fauna distributed within a cave? A study of the Ox Bel Ha System, Yucatan Peninsula, Mexico. Subterranean Biology 31: 15-28. https://doi.org/10.3897/subtbiol.31.34347
Figure 4 A Dendrogram and B non-metrical multidimensional scaling (nMDS) ordination plot, both resulting from the similarity matrix based on Jaccard's similarity index.
Figure 2 from: Bercea S, Năstase-Bucur R, Moldovan OT, Kenesz M, Constantin S (2019) Yearly microbial cycle of human exposed surfaces in show caves. Subterranean Biology 31: 1-14. https://doi.org/10.3897/subtbiol.31.34490
Figure 2 Distribution of culturable bacterial and fungal abundances on touched stalagmites from 2015 to 2016 in Ursilor (A) and Muierilor (B). TB, total aerobic bacteria; YM, yeasts and moulds; E.coli, Escherichiacoli.
Figure 3 from: Benítez S, Illife TM, Quiroz-Martínez B, Alvarez F (2019) How is the anchialine fauna distributed within a cave? A study of the Ox Bel Ha System, Yucatan Peninsula, Mexico. Subterranean Biology 31: 15-28. https://doi.org/10.3897/subtbiol.31.34347
Figure 3 Distribution of organisms by species in relation to depth in the four cenotes studied in the Ox Bel Ha cave: A, cenote Tábano; B, cenote Odyssey; C, cenote Muknal; and D, cenote Bang. The red band depicts the halocline, its width represents the thickness of the interface.
Figure 2 from: Niemiller ML, Inebnit T, Hinkle A, Jones BD, Jones M, Lamb J, Mann N, Miller B, Pinkley J, Pitts S, Sapkota KN, Slay ME (2019) Discovery of a new population of the federally endangered Alabama Cave Shrimp, Palaemonias alabamae Smalley, 1961, in northern Alabama. Subterranean Biology 32: 43-59. https://doi.org/10.3897/subtbiol.32.38280
Figure 2 Photographs of the cave shrimp from Fern Cave, Jackson County, Alabama in life: dorsal (A) and lateral views (B).
Figure 4 from: Niemiller ML, Inebnit T, Hinkle A, Jones BD, Jones M, Lamb J, Mann N, Miller B, Pinkley J, Pitts S, Sapkota KN, Slay ME (2019) Discovery of a new population of the federally endangered Alabama Cave Shrimp, Palaemonias alabamae Smalley, 1961, in northern Alabama. Subterranean Biology 32: 43-59. https://doi.org/10.3897/subtbiol.32.38280
Figure 4 Bayesian phylogram showing the relationships among the new Fern Cave population and other populations of P. alabamae and P. sp. nov. in Alabama inferred from the mitochondrial 16S ribosomal RNA locus. Posterior probabilities are to the left of the corresponding node.
Figure 1 from: Niemiller ML, Inebnit T, Hinkle A, Jones BD, Jones M, Lamb J, Mann N, Miller B, Pinkley J, Pitts S, Sapkota KN, Slay ME (2019) Discovery of a new population of the federally endangered Alabama Cave Shrimp, Palaemonias alabamae Smalley, 1961, in northern Alabama. Subterranean Biology 32: 43-59. https://doi.org/10.3897/subtbiol.32.38280
Figure 1 Distribution of the Alabama Cave Shrimp (Palaemonias alabamae) in Madison and Jackson counties, Alabama, USA. Carbonate strata are depicted in gray. Alabama Cave Shrimp sites are shown as blue dots.
Figure 3 from: Niemiller ML, Inebnit T, Hinkle A, Jones BD, Jones M, Lamb J, Mann N, Miller B, Pinkley J, Pitts S, Sapkota KN, Slay ME (2019) Discovery of a new population of the federally endangered Alabama Cave Shrimp, Palaemonias alabamae Smalley, 1961, in northern Alabama. Subterranean Biology 32: 43-59. https://doi.org/10.3897/subtbiol.32.38280
Figure 3 Joe Lamb and Bradley Jones searching for cave shrimp in an isolated pool near the Davidson Entrance to Fern Cave system on 25 August 2018.
Figures 5- 6 from: Pacheco Fonseca RM, de Paula CCP, Bichuette ME, Chagas Jr A (2019) First record of Amphoromorpha/ Basidiobolus fungus on centipedes (Geophilomorpha, Geophilidae) from Brazilian caves. Subterranean Biology 32: 61-67. https://doi.org/10.3897/subtbiol.32.38310
Figures 5- 6 (LES 0010593) 5 Details of the fungus Amphoromorpha/Basidiobolus on right leg 52 6 Details of the fungus Amphoromorpha/Basidiobolus on right leg 52. Scale bars: 200 μm.
Figures 1-4 from: Pacheco Fonseca RM, de Paula CCP, Bichuette ME, Chagas Jr A (2019) First record of Amphoromorpha/ Basidiobolus fungus on centipedes (Geophilomorpha, Geophilidae) from Brazilian caves. Subterranean Biology 32: 61-67. https://doi.org/10.3897/subtbiol.32.38310
Figures 1-4 Ribautia sp. Brölemann, 1909 (Chilopoda: Geophilomorpha: Geophilidae) 1. (LES 0016373) 1 Right leg 54 2 Left leg 55 3 Details of the fungus Amphoromorpha/Basidiobolus on right leg 54 4 Details of the fungus Amphoromorpha/Basidiobolus on the left leg 55. Scale bars: 50.0 μm;
Figure 1 from: Fernandes CS, Batalha MA, Bichuette ME (2019) Dark diversity in the dark: a new approach to subterranean conservation. Subterranean Biology 32: 69-80. https://doi.org/10.3897/subtbiol.32.38121
Figure 1 Caves studied in São Domingos karst area, state of Goiás, Brazil. 1. Lapa do Angélica; 2. Lapa do Bezerra; 3. Lapa da Terra Ronca II; 4. Lapa da Terra Ronca I (Terra Ronca System); 5. Lapa São Bernardo. NP2lj = sequences of sedimentary rocks with low metamorphism; NP2sl = metalimestones intercalated with silty clay to sandy sediments; NP2sh = predominantly silty-clay sediments.
Supplementary material 1 from: Fernandes CS, Batalha MA, Bichuette ME (2019) Dark diversity in the dark: a new approach to subterranean conservation. Subterranean Biology 32: 69-80. https://doi.org/10.3897/subtbiol.32.38121
: Data type: script
Figure 2 from: Fernandes CS, Batalha MA, Bichuette ME (2019) Dark diversity in the dark: a new approach to subterranean conservation. Subterranean Biology 32: 69-80. https://doi.org/10.3897/subtbiol.32.38121
Figure 2 Representative photographs of sampled caves. A Lapa do Angélica (photo: A. Gambarini) B entrance of Lapa da Terra Ronca I (photo: ME Bichuette) C Guano pile inside Lapa do São Bernardo (photo: A. Gambarini).
Figures 7-10 from: Shear WA, Steinmann DB (2019) Cave millipedes of the United States. XV. Coloradesmus gen. nov. (Diplopoda, Polydesmida, Macrosternodesmidae), and four new species from caves in Colorado, USA. Subterranean Biology 32: 15-32. https://doi.org/10.3897/subtbiol.32.38161
Figures 7-10 Coloradesmus species males. 7C. aquiliensis gonopods, anterior view 8C. aquiliensis gonopods, lateral view 9C. hopkinae collum, dorsal view 10C. hopkinae midbody ring, dorsal view. See text for explanation of labels.
ScienceDex guides
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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.