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193 results for “subterranean habitat”
Figure 3 from: Silva M, Rezende R, Lopes Ferreira R (2013) Detritus processing in lentic cave habitats in the neotropics. Subterranean Biology 11: 3-14. https://doi.org/10.3897/subtbiol.11.5107
Figure 3 - Temporal values of nitrogen and phosphorous (μg/kg) measured in plant discs exposed to decomposition in lentic habitats of the Santuário and Brega caves.
Figure 6 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 6 - Salamandra salamandra gallaica larvae predation upon Rana iberica tadpole on the 29 April (2012): A individual of salamander approaching tadpole instants before seizing it B salamander larval ingesting tadpole. Photos by Rosa GM.
Figure 4 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 4 - Egg and early life stages of Rana iberica inhabiting a drainage gallery in Serra da Estrela, Portugal: A egg mass stuck to underwater rock (28 January, 2012) B eggs' detail with new born tadpoles (one day old) C tadpole with dark pigmented colouration (Gosner stage 25; 11 March, 2012) D recently post-metamorphic individual (31 May, 2012). Photos by Rosa GM.
Figure 3 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 3 - Adult individuals of Rana iberica found inhabiting a drainage gallery in Serra da Estrela, Portugal: A male with typical lichen-shaped pattern on the back B female hidden in a crevice of the gallery C male climbing up the wall D couple in axillary amplexus in water E axillary amplexus out of the water. Photos by Rosa GM.
Figure 9 from: Perina G, Eberhard S (2012) Austromesocypris bluffensis sp. n. (Crustacea, Ostracoda, Cypridoidea, Scottiinae) from subterranean aquatic habitats in Tasmania, with a key to world species of the subfamily. ZooKeys 215: 1-31. https://doi.org/10.3897/zookeys.215.2987
Figure 9 - Austromesocypris bluffensis (Holotype): A shell, lateral view from the right side B A1 C two distal segments of the A1 D Mxl. Scales = 0.1 mm.
Figure 5 from: Perina G, Eberhard S (2012) Austromesocypris bluffensis sp. n. (Crustacea, Ostracoda, Cypridoidea, Scottiinae) from subterranean aquatic habitats in Tasmania, with a key to world species of the subfamily. ZooKeys 215: 1-31. https://doi.org/10.3897/zookeys.215.2987
Figure 5 - Damper Cave entrance and stream resurgence. Collection sites were located approximately 20 to 80 m inside the cave entrance, see next figures.
Figure 2 from: Perina G, Eberhard S (2012) Austromesocypris bluffensis sp. n. (Crustacea, Ostracoda, Cypridoidea, Scottiinae) from subterranean aquatic habitats in Tasmania, with a key to world species of the subfamily. ZooKeys 215: 1-31. https://doi.org/10.3897/zookeys.215.2987
Figure 2 - Precipitous Bluff (1140 m asl) showing heavily forested lower slopes which contain the karst and caves.
Figure 11 from: Perina G, Eberhard S (2012) Austromesocypris bluffensis sp. n. (Crustacea, Ostracoda, Cypridoidea, Scottiinae) from subterranean aquatic habitats in Tasmania, with a key to world species of the subfamily. ZooKeys 215: 1-31. https://doi.org/10.3897/zookeys.215.2987
Figure 11 - Austromesocypris bluffensis (Holotype): A UR, arrow indicating the genital process B attachment of the UR C L6 D forehead and upper lip E L7 F detail of the distal end of L7. Scales = 0.1 mm.
Figure 8 from: Perina G, Eberhard S (2012) Austromesocypris bluffensis sp. n. (Crustacea, Ostracoda, Cypridoidea, Scottiinae) from subterranean aquatic habitats in Tasmania, with a key to world species of the subfamily. ZooKeys 215: 1-31. https://doi.org/10.3897/zookeys.215.2987
Figure 8 - A, B Austromesocypris bluffensis (Holotype) C Austromesocypris sp. A shell, view from the right side B, C shell, view from the left side.
Figure 4 from: Gutjahr S, Schmidt S, Hahn H (2014) A proposal for a groundwater habitat classification at local scale. Subterranean Biology 14: 25-49. https://doi.org/10.3897/subtbiol.14.5429
Figure 4 - Boxplots on a Groundwater-Fauna-Index-values b percentage of stygobiotic species c Individuals per sample (one outlier omitted each in the groups GWrainfed, GWswb and Hyporheic) and d similarity [%] of faunistic communities in scaled ecological groups. Thresholds for alimony are marked by dashed lines (after Hahn 2006) in Fig. 4a and for faunistic stability (according to Gutjahr et al. 2013a) in Fig. 4d; n = number of samples, box = Interquartile range, vertical black bar = median; whiskers showing the lowest and highest non-outlier; circles showing outliers and stars extreme outliers.
Figure 1 from: Gutjahr S, Schmidt S, Hahn H (2014) A proposal for a groundwater habitat classification at local scale. Subterranean Biology 14: 25-49. https://doi.org/10.3897/subtbiol.14.5429
Figure 1 - Map of the study area (from Hahn 2006, modified). All sites were equipped with 4–5 trans-sectional groundwater wells. Boxes: The respective natural regions [Pfälzerwald Mountains = Central Uplands; Haardtrand and the Upper Rhine Plateau = South-Western Uplands (according to Stein et al. 2012)]. Abbreviations on overview map: A = Austria, B = Belgium, CH = Switzerland, CZ = Czech Republic, D = Germany, DK = Denmark, F = France, L = Luxembourg, NL = Netherlands, PL = Poland.
Figure 3 from: Gutjahr S, Schmidt S, Hahn H (2014) A proposal for a groundwater habitat classification at local scale. Subterranean Biology 14: 25-49. https://doi.org/10.3897/subtbiol.14.5429
Figure 3 - Standard deviations of environmental factors for each of the ecological groups. a Temperature [I =Stressed, II = GWstable, III = GWrainfed (recharged by precipitation), IV = GWswb (surface water body-recharged), V = Hyporheic] b DO-concentration, and c) detritus contents (estimated). Box = Interquartile range, vertical black bar = median; whiskers showing the lowest and highest non-outlier. Circles showing outliers and stars extreme outliers.
Figure 2 from: Gutjahr S, Schmidt S, Hahn H (2014) A proposal for a groundwater habitat classification at local scale. Subterranean Biology 14: 25-49. https://doi.org/10.3897/subtbiol.14.5429
Figure 2 - MDS (Multi-dimensional scaling) ordination of invertebrate assemblages of each trap (faunal data aggregated by mean for traps having 13–15 samplings). Vectors show physical and chemical parameters of groundwater explaining the distribution of traps within the MDS best (Fe = Total dissolved iron [mg l-1]). Naming of the traps in accordance with Table 1.
Supplementary material 2 from: Eusébio RP, Fonseca PE, Rebelo R, Mathias ML, Reboleira ASPS (2023) How to map potential mesovoid shallow substratum (MSS) habitats? A case study in colluvial MSS. Subterranean Biology 45: 141-156. https://doi.org/10.3897/subtbiol.45.96332
Literature review data Mesovoid Shallow Substrate's faunal communities
Figure 7 from: Balestra V, Lana E, Vanin S (2022) Observations on the habitat and feeding behaviour of the hypogean genus Eukoenenia (Palpigradi, Eukoeneniidae) in the Western Italian Alps. Subterranean Biology 42: 23-41. https://doi.org/10.3897/subtbiol.42.75784
Figure 7 Meal of Eukoenenia strinatii on dead springtail (photo by V. Balestra).
Figure 4 from: Balestra V, Lana E, Vanin S (2022) Observations on the habitat and feeding behaviour of the hypogean genus Eukoenenia (Palpigradi, Eukoeneniidae) in the Western Italian Alps. Subterranean Biology 42: 23-41. https://doi.org/10.3897/subtbiol.42.75784
Figure 4 Percentage of specimens found on different microhabitats.
Figure 6 from: Balestra V, Lana E, Vanin S (2022) Observations on the habitat and feeding behaviour of the hypogean genus Eukoenenia (Palpigradi, Eukoeneniidae) in the Western Italian Alps. Subterranean Biology 42: 23-41. https://doi.org/10.3897/subtbiol.42.75784
Figure 6 Approach and meal of Eukoenenia strinatii on Pseudosinella alpina (photos by E. Lana).
Figure 2 from: Balestra V, Lana E, Vanin S (2022) Observations on the habitat and feeding behaviour of the hypogean genus Eukoenenia (Palpigradi, Eukoeneniidae) in the Western Italian Alps. Subterranean Biology 42: 23-41. https://doi.org/10.3897/subtbiol.42.75784
Figure 2 Number of specimens observed for sampling site.
Figure 5 from: Baković N, Matoničkin Kepčija R, Siemensma FJ (2022) Transitional and small aquatic cave habitats diversification based on protist assemblages in the Veternica cave (Medvednica Mt., Croatia). Subterranean Biology 42: 43-60. https://doi.org/10.3897/subtbiol.42.78037
Figure 5 Taxon richness and abundance of protist taxa at the sites investigated.
Figure 1 from: Baković N, Matoničkin Kepčija R, Siemensma FJ (2022) Transitional and small aquatic cave habitats diversification based on protist assemblages in the Veternica cave (Medvednica Mt., Croatia). Subterranean Biology 42: 43-60. https://doi.org/10.3897/subtbiol.42.78037
Figure 1 Location of the Veternica cave.
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International Brain Laboratory public data
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OpenNeuro
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