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7,849 results for “Conservancy”
Figure 5 from: Onadeko A, Roedel M, Liedtke H, Barej M (2014) The rediscovery of Perret's toad, Amietophrynus perreti (Schiøtz, 1963) after more than 40 years, with comments on the species' phylogenetic placement and conservation status. Zoosystematics and Evolution 90(2): 113-119. https://doi.org/10.3897/zse.90.8234
Figure 5 - Systematic placement (Bayesian phylogenetic inference based on a mitochondrial fragment of the 16S rRNA gene) of Amietophrynus perreti within the genus Amietophrynus. Bayesian PP values are as follows: asterisks ('*') point to maximum support (1.00), full circles ('●') point to PP 0.95–0.99; empty circle ('○') point to PP 0.90–0.94; PP values below 0.90 not shown.
Figure 3 from: Onadeko A, Roedel M, Liedtke H, Barej M (2014) The rediscovery of Perret's toad, Amietophrynus perreti (Schiøtz, 1963) after more than 40 years, with comments on the species' phylogenetic placement and conservation status. Zoosystematics and Evolution 90(2): 113-119. https://doi.org/10.3897/zse.90.8234
Figure 3 - Sites around Idanre Hills surveyed for Amietophrynus perreti; green circles: toads recorded, red crosses: toads not found.
Figure 3 from: Espinasa L, Espinasa M, Fenolio D, Slay M, Niemiller M (2014) Distribution and conservation status of Speleonycta ozarkensis (Insecta, Zygentoma, Nicoletiidae) from caves of the Ozark Highlands of Arkansas and Oklahoma, USA. Subterranean Biology 14: 51-62. https://doi.org/10.3897/subtbiol.14.8275
Figure 3 - When Speleonycta ozarkensis was originally described (Espinasa et al. 2010), the diagnosis states that "tibia of second leg very stout (2 times longer than wide) with a large bulge with 3 distinctly long, sclerotized, and curved macrochaetae", as shown in (A). This description was based on a single specimen that had already been dissected and mounted in a fixed slide, with the legs isolated from each other. Examination of new specimens (B) shows that the order of legs was misidentified and that the modification is actually on the first leg pair.
Figure 4 from: Espinasa L, Espinasa M, Fenolio D, Slay M, Niemiller M (2014) Distribution and conservation status of Speleonycta ozarkensis (Insecta, Zygentoma, Nicoletiidae) from caves of the Ozark Highlands of Arkansas and Oklahoma, USA. Subterranean Biology 14: 51-62. https://doi.org/10.3897/subtbiol.14.8275
Figure 4 - Parasitic acari on thoracic notas of Speleonycta ozarkensis from AD85 Cave. They await taxonomic description.
Figure 1 from: Espinasa L, Espinasa M, Fenolio D, Slay M, Niemiller M (2014) Distribution and conservation status of Speleonycta ozarkensis (Insecta, Zygentoma, Nicoletiidae) from caves of the Ozark Highlands of Arkansas and Oklahoma, USA. Subterranean Biology 14: 51-62. https://doi.org/10.3897/subtbiol.14.8275
Figure 1 - Distribution of Speleonycta ozarkensis. Numbered localities correspond to those listed in Table 1.
Figure 3 from: Chetri M, Jhala YV, Jnawali SR, Subedi N, Dhakal M, Yumnam B (2016) Ancient Himalayan wolf (Canis lupus chanco) lineage in Upper Mustang of the Annapurna Conservation Area, Nepal. ZooKeys 582: 143-156. https://doi.org/10.3897/zookeys.582.5966
Figure 3 - Phylogenetic trees constructed using 229 bp of aligned CR sequence data. The values at nodes correspond to A bootstrap support > 50% in maximum likelihood (ML) and maximum parsimony (MP) analyses; and B Bayesian posterior probability > 0.50. Scat samples sequenced in this study are highlighted in bold. Four samples (D2137, D2138, D2139 and D2143) represented a novel haplotype HWF within the Himalayan wolf clade, while a fifth sample (D2140) matched with existing domestic dog haplotypes.
Figure 1 from: Chetri M, Jhala YV, Jnawali SR, Subedi N, Dhakal M, Yumnam B (2016) Ancient Himalayan wolf (Canis lupus chanco) lineage in Upper Mustang of the Annapurna Conservation Area, Nepal. ZooKeys 582: 143-156. https://doi.org/10.3897/zookeys.582.5966
Figure 1 - A Himalayan wolf photographed in Upper Mustang of Annapurna Conservation Area, Nepal (29.17356°N, 84.13422°E; datum WGS84, elevation 5,050 m) during May 2014.
Figure 2 from: Chetri M, Jhala YV, Jnawali SR, Subedi N, Dhakal M, Yumnam B (2016) Ancient Himalayan wolf (Canis lupus chanco) lineage in Upper Mustang of the Annapurna Conservation Area, Nepal. ZooKeys 582: 143-156. https://doi.org/10.3897/zookeys.582.5966
Figure 2 - Fecal sample and direct sighting locations of the Himalayan wolf in Upper Mustang of Annapurna Conservation Area, Nepal.
Figures 9-14 from: Martín-Vega D, Niederegger S (2015) Larval muscle attachment site (MAS) patterns are a conserved character among Piophilini flies (Diptera, Piophilidae). Deutsche Entomologische Zeitschrift 62(2): 239-245. https://doi.org/10.3897/dez.62.5685
Figures 9-14 - Muscular attachment sites in Piophilini larvae. 9. Liopiophila varipes (Meigen), third-instar larva, detail of abdominal row 5.3; 10. Prochyliza nigrimana (Meigen), third-instar larva, detail of abdominal row 8.3; 11. Stearibia nigriceps (Meigen), third-instar larva, detail of thoracic row 3.1; 12. Piophila casei (Linnaeus), third-instar larva, detail of abdominal row 5.3; 13. Piophila megastigmata McAlpine, third-instar larva, detail of abdominal row 8.3; 14. Centrophlebomyia furcata (Fabricius), third-instar larva, detail of thoracic row 3.1.
Figures 1-2 from: Martín-Vega D, Niederegger S (2015) Larval muscle attachment site (MAS) patterns are a conserved character among Piophilini flies (Diptera, Piophilidae). Deutsche Entomologische Zeitschrift 62(2): 239-245. https://doi.org/10.3897/dez.62.5685
Figures 1-2 - Liopiophila varipes (Meigen), third-instar larva. 1. Dorsal view of a pinned larva before dissection (left) and stained larval cuticle (right), showing the symmetrical muscular attachment sites on segments S2 to S11; 2. Detail of the abdominal segment S5 showing the label for each muscular attachment site pattern.
Figures 3-8 from: Martín-Vega D, Niederegger S (2015) Larval muscle attachment site (MAS) patterns are a conserved character among Piophilini flies (Diptera, Piophilidae). Deutsche Entomologische Zeitschrift 62(2): 239-245. https://doi.org/10.3897/dez.62.5685
Figures 3-8 - Condensed larval muscular attachment site patterns for six species of Piophilini. 3. Centrophlebomyia furcata (Fabricius). Larval length = 11.91±1.03 mm; diameter = 1.45±0.12 mm; n = 10; 4. Liopiophila varipes (Meigen). Larval length = 7.34±0.3 mm; diameter = 0.75±0.03 mm; n = 10; 5. Piophila casei (Linnaeus). Larval length = 7.43±0.42 mm; diameter = 0.87±0.05 mm; n = 10; 6. Piophila megastigmata McAlpine. Larval length = 7.69±0.28 mm; diameter = 0.82±0.03 mm; n = 10; 7. Prochyliza nigrimana (Meigen). Larval length = 6.61±0.24 mm; diameter = 0.72±0.02 mm; n = 10; 8. Stearibia nigriceps (Meigen). Larval length = 7.28±0.37 mm; diameter = 0.76±0.06 mm; n = 10.
Figure 1 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 1 - Distribution of 15 caves in the Atlantic Forest in the state of Espírito Santo, with invertebrate fauna inventoried in this study. Source: SOS Mata Atlântica (2011).
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 3 from: Minoli I, Morando M, Avila LJ (2015) Reptiles of Chubut province, Argentina: richness, diversity, conservation status and geographic distribution maps. ZooKeys 498: 103-126. https://doi.org/10.3897/zookeys.498.7476
Figure 3 - Imagery source: Blue Marble Next Generation (true-color), Web Map Service (WMS) layer from CREAF MAP SERVER (open-gis), EPSG: 4326. A Records of Cheloniidae, Dipsadidae and Viperidae. Green dot: Chelonia mydas; light blue dot: Erythrolamprus sagittifer sagittifer; magenta dot: Phalotris bilineatus; red dots: Bothrops ammodytoides; orange dots: Oxyrhopus rhombifer; black dots: Pseudotomodon trigonatus; blue dots: Philodryas patagoniensis; yellow dots: Philodryas trilineata; grey dots: Tachymenis chilensis B Records of lizards. Black dots: Amphisbaena plumbea; light blue dot: Amphisbaena kingii; red dot: Aurivela longicauda; magenta dots: Diplolaemus bibronii; blue dots: Diplolaemus darwinii; orange dots: Diplolaemus sexcinctus; yellow dots: Leiosaurus bellii; green dots: Pristidactylus nigroiugulus C Records of Homonota darwinii D Records of some Liolaemus species. Blue dots: Liolaemus bibronii; red dots: Liolaemus boulengeri E Records of some Liolaemus species. Magenta dots: Liolaemus camarones; black dots: Liolaemus canqueli; green dots: Liolaemus chehuachekenk; orange dots: Liolaemus darwinii; light blue dots: Liolaemus elongatus; yellow dots: Liolaemus fitzingerii; blue dots: Liolaemus gracilis; white dots: Liolaemus shehuen F Records of some Liolaemus species. Light blue dots: Liolaemus kingii; red dot: Liolaemus kriegi; yellow dots: Liolaemus lineomaculatus; green dots: Liolaemus melanops; magenta dots: Liolaemus morandae; blue dots: Liolaemus petrophilus G Records of some Liolaemus species. Magenta dots: Liolaemus pictus argentinus; orange dots: Liolaemus rothi; green dots: Liolaemus senguer; yellow dot: Liolaemus somuncurae; light blue dots: Liolaemus telsen; blue dots: Liolaemus uptoni; red dots: Liolaemus xanthoviridis H Records of Phymaturus species. Red dots: Phymaturus calcogaster; white dot: Phymaturus camilae; green dot: Phymaturus castillensis; blue dot: Phymaturus felixi; yellow dots: Phymaturus indistinctus; light blue dots: Phymaturus patagonicus; orange dots: Phymaturus somuncurensis; magenta dot: Phymaturus videlai.
ScienceDex guides
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Allen Brain Atlas
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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.