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1,118 results for “subterranean biology”
Figure 8 from: Souza-Silva M, Ferreira RL (2015) Cave invertebrates in Espírito Santo state, Brazil: a primary analysis of endemism, threats and conservation priorities. Subterranean Biology 16: 79-102. https://doi.org/10.3897/subtbiol.16.5227
Figure 8 - Human alterations in caves of Espírito Santo, Brazil. A religious use in granite cave in Venda Nova dos Imigrantes B transformation of granitic cave into a church in Itaimbé-Itaguassu C deforestation surrounding cave in Ecoporanga, D drainage exploitation in granite cave near Pedro Canário E use of cave as goat corral F road construction destroying cave chambers in Vargem Alta G and I Limoeiro cave entrance with religious and tourist use in Conceição de Castelo H using limestone cave as a timber-yard in Vargem Alta.
Figure 7 from: Souza-Silva M, Ferreira RL (2015) Cave invertebrates in Espírito Santo state, Brazil: a primary analysis of endemism, threats and conservation priorities. Subterranean Biology 16: 79-102. https://doi.org/10.3897/subtbiol.16.5227
Figure 7 - Almost significant differences between the diversity and total and relative richness of invertebrates in caves that develop in carbonate rocks and magma in the state of Espírito Santo. Average, ± SE, ± SD.
Figure 3 from: Souza-Silva M, Ferreira RL (2015) Cave invertebrates in Espírito Santo state, Brazil: a primary analysis of endemism, threats and conservation priorities. Subterranean Biology 16: 79-102. https://doi.org/10.3897/subtbiol.16.5227
Figure 3 - Some of the troglomorphic invertebrates sampled in 15 caves in Atlantic forest at Espírito Santo state, Brazil. A Escadabiidae, B Trachelipodidae, C Pseudonannolene sp., D Cryptodesmidae, E Trichopolidesmydae, F Zygentoma, G Trichorhina sp.
Figure 2 from: Souza-Silva M, Ferreira RL (2015) Cave invertebrates in Espírito Santo state, Brazil: a primary analysis of endemism, threats and conservation priorities. Subterranean Biology 16: 79-102. https://doi.org/10.3897/subtbiol.16.5227
Figure 2 - Composition and richness of invertebrate taxa collected in 15 caves in the state of Espírito Santo, Brazil.
Figure 6 from: Souza-Silva M, Ferreira RL (2015) Cave invertebrates in Espírito Santo state, Brazil: a primary analysis of endemism, threats and conservation priorities. Subterranean Biology 16: 79-102. https://doi.org/10.3897/subtbiol.16.5227
Figure 6 - A Significant relationship of the increased richness of collected invertebrates with the increase in size of caves in limestone and granitic rocks and B no significant relationship without limestone caves in the state of Espírito Santo.
Figure 9 from: Souza-Silva M, Ferreira RL (2015) Cave invertebrates in Espírito Santo state, Brazil: a primary analysis of endemism, threats and conservation priorities. Subterranean Biology 16: 79-102. https://doi.org/10.3897/subtbiol.16.5227
Figure 9 - A Distribution of cave biological relevance B cave impacts category and C cave fauna vulnerability in the state of Espírito Santo. Gray shading on maps represents remnants of the Atlantic Forest.
Figure 5 from: Souza-Silva M, Ferreira RL (2015) Cave invertebrates in Espírito Santo state, Brazil: a primary analysis of endemism, threats and conservation priorities. Subterranean Biology 16: 79-102. https://doi.org/10.3897/subtbiol.16.5227
Figure 5 - A Distribution of caves, B relative richness and C total richness of the 15 caves of the state of Espírito Santo, Brazil.
Figure 7 from: Rantin B, Bichuette M (2015) Spontaneous behavior of basal Copionodontinae cave catfishes from Brazil (Teleostei, Siluriformes, Trichomycteridae). Subterranean Biology 16: 61-77. https://doi.org/10.3897/subtbiol.16.5180
Figure 7 - Box-plot (medians and standard deviations on Y axis) showing the spontaneous behavioral categories variability for Copionodontinae catfishes from Chapada Diamantina. o, outliers; dark blue, hidden; light blue, stationary; dark green, bottom swim; light green, wall swim; dark yellow, midwater swim; light yellow, surface swim.
Figure 6 from: Rantin B, Bichuette M (2015) Spontaneous behavior of basal Copionodontinae cave catfishes from Brazil (Teleostei, Siluriformes, Trichomycteridae). Subterranean Biology 16: 61-77. https://doi.org/10.3897/subtbiol.16.5180
Figure 6 - Individual frequencies of the behavioral categories recorded for copionodontine catfishes from Chapada Diamantina. Dark blue, hidden; light blue, stationary; dark green, bottom swim; light green, wall swim; dark yellow, midwater swim; light yellow, surface swim a Glaphyropoma spinosum b Copionodon sp. n. c Copionodon pecten.
Figure 4 from: Rantin B, Bichuette M (2015) Spontaneous behavior of basal Copionodontinae cave catfishes from Brazil (Teleostei, Siluriformes, Trichomycteridae). Subterranean Biology 16: 61-77. https://doi.org/10.3897/subtbiol.16.5180
Figure 4 - Copionodon sp. n. – fixed specimen, left lateral view and dorsal view (Photography: Pedro Pereira Rizzato). Standard length: 38.9 mm.
Figure 3 from: Rantin B, Bichuette M (2015) Spontaneous behavior of basal Copionodontinae cave catfishes from Brazil (Teleostei, Siluriformes, Trichomycteridae). Subterranean Biology 16: 61-77. https://doi.org/10.3897/subtbiol.16.5180
Figure 3 - Glaphyropoma spinosum – fixed specimen, left lateral view and dorsal view (Photography: Pedro Pereira Rizzato). Standard length: 47.6 mm.
Figure 2 from: Rantin B, Bichuette M (2015) Spontaneous behavior of basal Copionodontinae cave catfishes from Brazil (Teleostei, Siluriformes, Trichomycteridae). Subterranean Biology 16: 61-77. https://doi.org/10.3897/subtbiol.16.5180
Figure 2 - Spatial behavior and natural habitats of copionodontine catfishes from Chapada Diamantina a Glaphyropoma spinosum (black arrow) swimming close to the bottom in a pool (Photography: Maria Elina Bichuette) b small stream in the cave environment, place where Copionodon sp. n. occurs (Photography: Jonas Eduardo Gallão) c natural pool where Copionodon pecten forages under the day-light (Photography: Bianca Rantin).
Figure 1 from: Rantin B, Bichuette M (2015) Spontaneous behavior of basal Copionodontinae cave catfishes from Brazil (Teleostei, Siluriformes, Trichomycteridae). Subterranean Biology 16: 61-77. https://doi.org/10.3897/subtbiol.16.5180
Figure 1 - Copionodontinae occurrence area. Map of Brazil, indicating the Chapada Diamantina region, endemic area of Copionodontinae catfishes. In green, the Chapada Diamantina National Park (CDNP), eastern Brazil. Author: Diego Monteiro Von Schimonsky.
Figure 5 from: Rantin B, Bichuette M (2015) Spontaneous behavior of basal Copionodontinae cave catfishes from Brazil (Teleostei, Siluriformes, Trichomycteridae). Subterranean Biology 16: 61-77. https://doi.org/10.3897/subtbiol.16.5180
Figure 5 - Copionodon pecten – fixed specimen, left lateral view and dorsal view (Photography: Pedro Pereira Rizzato). Standard length: 43.2 mm.
Figure 4 from: Ferreira RL, Martins VM, Paixão ER, Silva MS (2015) Spatial and temporal fluctuations of the abundance of Neotropical cave-dwelling moth Hypena sp. (Noctuidae, Lepidoptera) influenced by temperature and humidity. Subterranean Biology 16: 47-60. https://doi.org/10.3897/subtbiol.16.5137
Figure 4 - Spatial distribution maps of Hypena sp. demonstrating different densities between seasons. In the dry seasons (17/07/1999 and 10/07/2000) individuals are located in the deepest region of the cave, an opposite pattern during rainy seasons (16/01/2000 and 19/01/2001) when the population of individuals becomes denser in the region near the cave entrance. Blue colors indicate low densities while light yellow colors indicate high densities.
Figure 1 from: Ferreira RL, Martins VM, Paixão ER, Silva MS (2015) Spatial and temporal fluctuations of the abundance of Neotropical cave-dwelling moth Hypena sp. (Noctuidae, Lepidoptera) influenced by temperature and humidity. Subterranean Biology 16: 47-60. https://doi.org/10.3897/subtbiol.16.5137
Figure 1 - A Photograph indicating the cave entrance and the surrounding region, whose native forest was turned into pasture B Conduit located in the area near the entrance C Individuals of Hypena sp. resting on the cave wall.
Figure 3 from: Ferreira RL, Martins VM, Paixão ER, Silva MS (2015) Spatial and temporal fluctuations of the abundance of Neotropical cave-dwelling moth Hypena sp. (Noctuidae, Lepidoptera) influenced by temperature and humidity. Subterranean Biology 16: 47-60. https://doi.org/10.3897/subtbiol.16.5137
Figure 3 - Spatial Point Pattern Analysis of the second monitoring (January 2000). A Dot map and (B), shows the estimations of the function K (r is the distance argument, Dashed line corresponds to the theoretical value of this function is Complete Spatial Randomness and solid lineis the Observed value of the K function for the date pattern) C Map Kernel Estimates of intensity.
Figure 2 from: Ferreira RL, Martins VM, Paixão ER, Silva MS (2015) Spatial and temporal fluctuations of the abundance of Neotropical cave-dwelling moth Hypena sp. (Noctuidae, Lepidoptera) influenced by temperature and humidity. Subterranean Biology 16: 47-60. https://doi.org/10.3897/subtbiol.16.5137
Figure 2 - A Variation in temperature and humidity along the Taboa cave, showing a tendency to stabilize in the deeper parts of the cave. The table shows the section in which the Hypena sp specimens were collected (B) Change in abundance over the transects, the arrow indicates the spatial extent where the effects of the surface seasonality promote decrease and expansion in the population distribution.
Figure 5 from: Lewis JJ, Sawicki TR (2016) Mexistenasellus floridensis sp. n., the first stenasellid isopod discovered from the Floridan aquifer (Crustacea, Isopoda, Asellota). Subterranean Biology 17: 121-132. https://doi.org/10.3897/subtbiol.17.7703
Figure 5 - Mexistenasellus floridensis sp. n. pleopods, male except 4e: a pleopod 1 b pleopod 2 c same, tip of endopodite, anterior d same, posterior e pleopod 2 f pleopod 3 g pleopod 4 h pleopod 5.
Figure 3 from: Lewis JJ, Sawicki TR (2016) Mexistenasellus floridensis sp. n., the first stenasellid isopod discovered from the Floridan aquifer (Crustacea, Isopoda, Asellota). Subterranean Biology 17: 121-132. https://doi.org/10.3897/subtbiol.17.7703
Figure 3 - Mexistenasellus floridensis sp. n., mouthparts: a maxilla 1 b mandible, right, incisors c mandible, left, incisors and lacinia d mandibular palp e maxilliped.
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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.