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Figure 2 from: Bichuette ME, Trajano E (2018) Diversity of Potamolithus (Littorinimorpha, Truncatelloidea) in a high-diversity spot for troglobites in southeastern Brazil: role of habitat fragmentation in the origin of subterranean fauna, and conservation status. Subterranean Biology 25: 61-88. https://doi.org/10.3897/subtbiol.25.23778

Figure 2 Landscape (Atlantic Rainforest) (A), Potamolithus sp. 5 in natural habitat, Santana cave (B) and subterranean streams (C, D) from Alto Ribeira karst area, Southeastern Brazil. Photographs: PP Rizzato (A, C, D), A Gambarini (B).

opencc-by-4.0May 2018View details →
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Figure 10 from: Bichuette ME, Trajano E (2018) Diversity of Potamolithus (Littorinimorpha, Truncatelloidea) in a high-diversity spot for troglobites in southeastern Brazil: role of habitat fragmentation in the origin of subterranean fauna, and conservation status. Subterranean Biology 25: 61-88. https://doi.org/10.3897/subtbiol.25.23778

Figure 10 Boxplots showing shell widths on Potamolithus spp. Horizontal Bar, median; vertical bar, whiskers with minimal and maximum observations. 1 P. ribeirensis 2 Potamolithus sp. 1 3 P. karsticus 4 Potamolithus sp. 2 5 Potamolithus sp. 3 6 Potamolithus sp. 4 7 Potamolithus sp. 5 8 Potamolithus sp. 6 9 Potamolithus sp. 7 10 P. troglobius 11 Potamolithus aff. troglobius 12 Potamolithus sp. 8 13 Potamolithus sp. 9 14 Potamolithus sp. 10 15 Potamolithus sp. 11 16 Potamolithus sp. 12. Black bars, epigean species; gray bars, troglophilic species; white bars, troglobitic species; circles, outliers; *, extremes.

opencc-by-4.0May 2018View details →
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Figure 3 from: Bichuette ME, Trajano E (2018) Diversity of Potamolithus (Littorinimorpha, Truncatelloidea) in a high-diversity spot for troglobites in southeastern Brazil: role of habitat fragmentation in the origin of subterranean fauna, and conservation status. Subterranean Biology 25: 61-88. https://doi.org/10.3897/subtbiol.25.23778

Figure 3 Schematic intestine forms observed in Potamolithus species from Alto Ribeira karst area, Southeastern Brazil. Abapertural view.

opencc-by-4.0May 2018View details →
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Figure 1 from: Bichuette ME, Trajano E (2018) Diversity of Potamolithus (Littorinimorpha, Truncatelloidea) in a high-diversity spot for troglobites in southeastern Brazil: role of habitat fragmentation in the origin of subterranean fauna, and conservation status. Subterranean Biology 25: 61-88. https://doi.org/10.3897/subtbiol.25.23778

Figure 1 Map showing the surveyed localities (basins, microbasins and caves) from Alto Ribeira karst area, Southeastern Brazil. Some localities are approximated (*) (Author: DM von Schimonsky). Caves: A1 – Aranhas, A2 – Chapéu Mirim I, A3 – Chapéu, A4 – Chapéu Mirim II, A5 – Temimina II, A6 – Gurutuva, A7 – Córrego Seco, A8 – Fendão, A9 – Paiva, A10 – Jane Mansfield, A11 – Minotauro; B1 – Areias de Cima, B2 – Areias de Baixo, B3 – Ressurgência das Areias de Água Quente; C – Ouro Grosso; D – Alambari de Baixo; E – Água Suja; F1 – Pérolas, F2 – Santana; G1 – Casa de Pedra, G2 – Água Sumida; H – Tapagem; I1 – Morro Preto, I2 – Couto; J – Pescaria; K* – Betari de Baixo; L – Jeremias; M – Colorida; N – Calcário Branco; O – Alambari de Cima. Epigean streams: a – Ouro Grosso; b – Alambari; c – Água Suja; d – Roncador; e – Maximiano; f – Ostras; g – Calcário Branco; h – Iporanga; i1 – Betari, i2 – Água Quente, i3 – Morro Preto; j1 – Bocaina, j2 – Espírito Santo, j3 – Temimina, j4 – Pescaria, j5 – Lageado, j6 – Pilões, j7 – Ribeira, j8 – Cutia de Cima.

opencc-by-4.0May 2018View details →
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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.

opencc-by-4.0Jul 2019View details →
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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.

opencc-by-4.0Jul 2019View details →
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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.

opencc-by-4.0Jul 2019View details →
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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.

opencc-by-4.0Jul 2019View details →
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Figure 3 in Cryptops (Trigonocryptops) didi sp. n. (Chilopoda: Scolopendromorpha: Cryptopidae): expanding the cryptopid biodiversity in a Brazilian hotspot of subterranean fauna

Figure 3. Cryptops (T.) didi sp. n. Holotype (LES – UFSCAR 0026263). Habitus dorsal.

opennotspecifiedAug 2024View details →
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Table 1 in Cryptops (Trigonocryptops) didi sp. n. (Chilopoda: Scolopendromorpha: Cryptopidae): expanding the cryptopid biodiversity in a Brazilian hotspot of subterranean fauna

<p><b>Table 1.</b> Diagnostic characters of three species of Brazilian <i>Cryptops</i> considered in this study.</p><table><tbody><tr><th></th><th><i>Cryptops</i> (<i>T</i>.) <i>iheringi</i></th><th><i>C</i>. (<i>C</i>.) <i>iporangensis</i></th><th><i>Cryptops</i> (<i>T</i>.) <i>didi</i> <b>sp. n.</b></th></tr></tbody><tbody><tr><th>Antennae Sutures in first antennal article</th><td>Extend to tergite 3; 13&ndash;15 articles Irregular, proximal/ventral, extend to dorsal aspect of the article</td><td>Extend to tergite 6; 17 articles Suture proximal/ventral, inverted Y</td><td>Extend to tergite 8; 17 articles Irregular, proximal/ventral, extend to dorsal aspect of the article</td></tr><tr><th>Forcipular coxosternite</th><td>Convex on each side, row of bristles 13 + 13 Median suture extends to 1/2 of the coxosternum</td><td>Convex on each side, row of 7 + 7 marginal bristles</td><td>Convex on each side, with a row of 9 + 9 marginal bristles, Median longitudinal suture extending to 1/3 of the coxosternum</td></tr><tr><th>Sutures in tergite 1</th><td>Anterior transverse suture, W-shaped suture, and lateral sutures</td><td>Anterior transverse suture</td><td>Anterior transverse suture; lateral and posterior sutures that connect to the paramedian sutures</td></tr><tr><th>Paramedian sutures</th><td>Complete on tergites 1&ndash;20, lateral grooves 5&ndash;18</td><td>Incomplete on tergites 2&ndash;19</td><td>Complete on tergites 1&ndash;20</td></tr><tr><th>Anterior oblique sutures</th><td>Present on tergites 3&ndash;8</td><td>Absent</td><td>Present on tergites 3&ndash;5</td></tr><tr><th>Trigonal sutures on sternites</th><td>Present on sternites 4&ndash;15</td><td>Absent</td><td>Present at sternites 4&ndash;6</td></tr><tr><th>Ultimate legs</th><td>No distal spinose processes; 12(13) + 4(5) saw teeth</td><td>A pair of distal spinose processes on the prefemur, femur, and tibia; 10 + 5 saw teeth</td><td>A pair of distal spinose processes on the prefemur, femur, and tibia; 19 + 7 or 3 + 21 + 8 saw teeth</td></tr></tbody></table>

opennotspecifiedAug 2024View details →
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Figures 27-29 from: Giachino PM, Eberhard S, Perina G (2021) A rich fauna of subterranean short-range endemic Anillini (Coleoptera, Carabidae, Trechinae) from semi-arid regions of Western Australia. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 269-337. https://doi.org/10.3897/zookeys.1044.58844

Figures 27-29 Magnanillus serenitatis sp. nov., HT ♂ 27 habitus 28 right metafemur and metatrochanter in ventral view 29 aedeagus in lateral view. Scale bars: 0.1 mm.

opencc-by-4.0Jun 2021View details →
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Figures 24-26 from: Giachino PM, Eberhard S, Perina G (2021) A rich fauna of subterranean short-range endemic Anillini (Coleoptera, Carabidae, Trechinae) from semi-arid regions of Western Australia. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 269-337. https://doi.org/10.3897/zookeys.1044.58844

Figures 24-26 Magnanillus regalis sp. nov., HT ♂ 24 habitus 25 right metafemur and metatrochanter in ventral view 26 aedeagus in lateral view. Scale bars: 0.1 mm.

opencc-by-4.0Jun 2021View details →
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Figures 21-23 from: Giachino PM, Eberhard S, Perina G (2021) A rich fauna of subterranean short-range endemic Anillini (Coleoptera, Carabidae, Trechinae) from semi-arid regions of Western Australia. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 269-337. https://doi.org/10.3897/zookeys.1044.58844

Figures 21-23 Magnanillus salomonis sp. nov., HT ♂ 21 habitus 22 left metafemur and metatrochanter in dorsal view 23 aedeagus in lateral view. Scale bars: 0.1 mm.

opencc-by-4.0Jun 2021View details →
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Figures 8- 9 from: Giachino PM, Eberhard S, Perina G (2021) A rich fauna of subterranean short-range endemic Anillini (Coleoptera, Carabidae, Trechinae) from semi-arid regions of Western Australia. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 269-337. https://doi.org/10.3897/zookeys.1044.58844

Figures 8- 9 Gregorydytes ophthalmianus gen. et sp. nov., HT ♂ 8 habitus 9 aedeagus in lateral view. Scale bars: 0.1 mm.

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Figures 10-14 from: Giachino PM, Eberhard S, Perina G (2021) A rich fauna of subterranean short-range endemic Anillini (Coleoptera, Carabidae, Trechinae) from semi-arid regions of Western Australia. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 269-337. https://doi.org/10.3897/zookeys.1044.58844

Figures 10-14 Pilbaraphanus gen. et spp. nov., habitus (10, 13) right metafemur and metatrochanter in ventral view (11, 14) aedeagus in lateral view (12) 10–12P. chichesterianus sp. nov., HT ♂ 13, 14P. bilybarianus sp. nov. HT ♀. Scale bars: 0.1 mm.

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Figures 4-7 from: Giachino PM, Eberhard S, Perina G (2021) A rich fauna of subterranean short-range endemic Anillini (Coleoptera, Carabidae, Trechinae) from semi-arid regions of Western Australia. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 269-337. https://doi.org/10.3897/zookeys.1044.58844

Figures 4-7 Gracilanillus spp.: habitus HT ♀ (4, 6) left metafemur and metatrochanter in ventral view HT ♀ (5, 7) 4, 5G. hirsutus sp. nov. 6, 7G. pannawonicanus sp. nov. Scale bars: 0.1 mm.

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Figure 52 from: Giachino PM, Eberhard S, Perina G (2021) A rich fauna of subterranean short-range endemic Anillini (Coleoptera, Carabidae, Trechinae) from semi-arid regions of Western Australia. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 269-337. https://doi.org/10.3897/zookeys.1044.58844

Figure 52 Distribution of all currently described Anillini species in Western Australia. See Fig. 53 for an enlargement of Pilbara region. Species described by Baehr and Main (2016) are marked with an asterisk (*).

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Figures 49-51 from: Giachino PM, Eberhard S, Perina G (2021) A rich fauna of subterranean short-range endemic Anillini (Coleoptera, Carabidae, Trechinae) from semi-arid regions of Western Australia. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 269-337. https://doi.org/10.3897/zookeys.1044.58844

Figures 49-51 Angustanillus armatus sp. nov., HT ♂ 49 habitus 50 left metafemur and metatrochanter in dorsal view 51 aedeagus in lateral view. Scale bars: 0.1 mm.

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Figures 46-48 from: Giachino PM, Eberhard S, Perina G (2021) A rich fauna of subterranean short-range endemic Anillini (Coleoptera, Carabidae, Trechinae) from semi-arid regions of Western Australia. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 269-337. https://doi.org/10.3897/zookeys.1044.58844

Figures 46-48 Bylibaraphanus gen. et spp. nov., habitus (46, 48) aedeagus in lateral view (47) 46, 47B. currani (Baehr and Main), ♂ 48B. cundalinianus sp. nov., HT ♀. Scale bars: 0.1 mm.

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Figures 43-45 from: Giachino PM, Eberhard S, Perina G (2021) A rich fauna of subterranean short-range endemic Anillini (Coleoptera, Carabidae, Trechinae) from semi-arid regions of Western Australia. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 269-337. https://doi.org/10.3897/zookeys.1044.58844

Figures 43-45 Pilbaradytes gen. et spp. nov., habitus (43, 45) aedeagus in lateral view (44) 43, 44P. abydosianus sp. nov., HT ♂ 45P. webberianus sp. nov., HT ♀. Scale bars: 0.1 mm.

opencc-by-4.0Jun 2021View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record