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Figure 1 from: Hesselberg T, Simonsen D (2019) A comparison of morphology and web geometry between hypogean and epigean species of Metellina orb spiders (family Tetragnathidae). Subterranean Biology 32: 1-13. https://doi.org/10.3897/subtbiol.32.36222
Figure 1 Principal component ordination plots of morphological and web parameters of Metellina merianae (red circle) and Metellina mengei (blue triangle). A Morphological variables (total length, cephalothorax width, patella-tibia length of leg I and leg III). The combined proportion of variance explained by PCA1 and PCA2 was 98%. B Web parameters (number of spirals, number of radii, vertical length of web, horizontal length of web and hub diameter). The combined proportion of variance explained by PCA1 and PCA2 was 78%.
Figure 1 from: Jakšová P, Ľuptáčik P, Miklisová D (2019) Distribution of Oribatida (Acari) along a depth gradient in forested scree slopes. Subterranean Biology 31: 29-48. https://doi.org/10.3897/subtbiol.31.36241
Figure 1 Localities of samplings. 1 – Ardovská jaskyňa Cave, 2 – Belinské skaly Rocks, 3 – Drienčanský kras Karst, 4 – Malý Ružínok Valley, 5 – Silická ľadnica Cave.
Figure 2 from: Hesselberg T, Simonsen D (2019) A comparison of morphology and web geometry between hypogean and epigean species of Metellina orb spiders (family Tetragnathidae). Subterranean Biology 32: 1-13. https://doi.org/10.3897/subtbiol.32.36222
Figure 2 Area of webs of Metellina merianae in response to spider size and position in cave. A The number of radii in the web as a function of cephalothorax width of the resident spider. Not significant. B The number of radii in the web as a function of its distance from the cave entrance. Not significant. C The area of the capture spiral as a function of cephalothorax width. Significant. The grey line represents the equation (y = 169x – 81, R2 = 0.31) arising from a simple linear regression. D The area of the capture spiral in the web as a function of its distance from the cave entrance. Not significant.
Figure 9 from: Ando K (2019) The study of amphipods in rimstone pools of Akiyoshi-do Cave, Japan. Subterranean Biology 32: 81-94. https://doi.org/10.3897/subtbiol.32.35031
Figure 9 Result of CCA analysis on the amphipod abundances and water characteristics. TN: total nitrogen, TP: total phosphorus, TB: total number of bacteria, TVB: total number of viable bacteria. Other symbols mean pools surveyed in each season by "month-pool number": for example, 5-CH1 corresponds to CH1 pool surveyed in May.
Figure 5 from: Ando K (2019) The study of amphipods in rimstone pools of Akiyoshi-do Cave, Japan. Subterranean Biology 32: 81-94. https://doi.org/10.3897/subtbiol.32.35031
Figure 5 Pools with arrows pointing the flowing directions. Water from the walls and drips was supplied to CH4 and water flowed to CH2 and CH1 via CH5. Pumped cave river water was supplied to CH8 and CH9 and water flowed to CH6 and CH7.
Figure 8 from: Ando K (2019) The study of amphipods in rimstone pools of Akiyoshi-do Cave, Japan. Subterranean Biology 32: 81-94. https://doi.org/10.3897/subtbiol.32.35031
Figure 8 Fluctuation of the population density of Gammarus nipponensis in the type C pools (1971–1975, 2015–2016).
Figure 7 from: Ando K (2019) The study of amphipods in rimstone pools of Akiyoshi-do Cave, Japan. Subterranean Biology 32: 81-94. https://doi.org/10.3897/subtbiol.32.35031
Figure 7 Fluctuation of the population density of Gammarus nipponensis in the type B pools (1971–1975, 2015–2016).
Figure 6 from: Ando K (2019) The study of amphipods in rimstone pools of Akiyoshi-do Cave, Japan. Subterranean Biology 32: 81-94. https://doi.org/10.3897/subtbiol.32.35031
Figure 6 Fluctuation of the population densities of Pseudocrangonyx akatsukai and Gammarus nipponensis in the type A pools (1971–1975, 2015–2016).
Figure 2 from: Ando K (2019) The study of amphipods in rimstone pools of Akiyoshi-do Cave, Japan. Subterranean Biology 32: 81-94. https://doi.org/10.3897/subtbiol.32.35031
Figure 2 Location of the Akiyoshi-do Cave in Japan and of the surveyed pools inside the cave. The cave river flows to the south. The map of Akiyoshi-do Cave was drawn based on karusuto.com (https://akiyoshido.karusuto.com/html/guide/).
Figure 4 from: Kunt KBB, Elverici M, Yağmur EA, Özkütük RS (2019) Kut gen. nov., a new troglomorphic spider genus from Turkey (Araneae, Dysderidae). Subterranean Biology 32: 95-109. https://doi.org/10.3897/subtbiol.32.46534
Figure 4 Kut dimensis sp. nov. A carapace B chelicerae C prosoma D male palp, retrolateral view E ditto, prolateral view F ditto, nearly anterior view G vulva, dorsal view H ditto, ventral view. Scale bars: 0.5 (D), 0.125 (G).
Figure 1 from: Kunt KBB, Elverici M, Yağmur EA, Özkütük RS (2019) Kut gen. nov., a new troglomorphic spider genus from Turkey (Araneae, Dysderidae). Subterranean Biology 32: 95-109. https://doi.org/10.3897/subtbiol.32.46534
Figure 1 Kut troglophilus (Brignoli, 1978) comb. nov. A carapace B chelicerae C prosoma D male palp, retrolateral view E ditto, prolateral view F ditto, nearly retrolateral view G vulva, dorsal view H ditto, ventral view. Scale bars: 0.5 (D), 0.125 (G).
Figure 2 from: Kunt KBB, Elverici M, Yağmur EA, Özkütük RS (2019) Kut gen. nov., a new troglomorphic spider genus from Turkey (Araneae, Dysderidae). Subterranean Biology 32: 95-109. https://doi.org/10.3897/subtbiol.32.46534
Figure 2 Kut izmiricus sp. nov. A carapace B chelicerae C prosoma D male palp, retrolateral view E ditto, prolateral view F ditto, nearly prolateral view G vulva, dorsal view H ditto, ventral view. Scale bars: 0.5 (D), 0.125 (G).
Figure 2. The effective population size through recent time for 3 in Comparative analyses of past population dynamics between two subterranean zokor species and the response to climate changes
Figure 2. The effective population size through recent time for 3 clades of plateau zokor (Eospalax baileyi).
FIGURE 2 in A new subterranean species of PHREATOBIUS Goeldi, 1905 (Siluriformes, INCERTAE SEDIS) from the Southwestern Amazon basin
FIGURE 2: Distribution of species of Phreatobius
Marine recalcitrant dissolved organic matter gained by processing at sandy subterranean estuaries
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FIGURE 1 in Flowering in darkness: a new species of subterranean orchid Rhizanthella (Orchidaceae; Orchidoideae; Diurideae) from Western Australia
FIGURE 1. Phenology of Rhizanthella. Illustrated by K. Dixon.
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.
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; 13–15 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 1–20, lateral grooves 5–18</td><td>Incomplete on tergites 2–19</td><td>Complete on tergites 1–20</td></tr><tr><th>Anterior oblique sutures</th><td>Present on tergites 3–8</td><td>Absent</td><td>Present on tergites 3–5</td></tr><tr><th>Trigonal sutures on sternites</th><td>Present on sternites 4–15</td><td>Absent</td><td>Present at sternites 4–6</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>
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.
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.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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