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80 results for “subterranean biodiversity”
Figures 1-3 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 1-3 Erwinanillus baehri gen. et sp. nov., HT ♂. 1 habitus 2 right metafemur and metatrochanter in ventral view 3 aedeagus in left lateral view. Scale bars: 0.1 mm.
Figures 34- 35 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 34- 35 Kimberleytyphlus carrboydianus gen. et sp. nov., HT ♂ 34 habitus 35 aedeagus in lateral view. Scale bars: 0.1 mm.
Figures 30-33 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 30-33 Neoillaphanus callawanus gen. et sp. nov. 30 habitus HT ♂ 31 right metafemor and metatrochanter in ventral view, HT ♂ 32 aedeagus in lateral view, HT ♂ 33 aedeagus in lateral view, PT ♂. Scale bars: 0.1 mm.
Figure 10 from: Glanville K, Schulz C, Tomlinson M, Butler D (2016) Biodiversity and biogeography of groundwater invertebrates in Queensland, Australia. Subterranean Biology 17: 55-76. https://doi.org/10.3897/subtbiol.17.7542
Figure 10 - Scatterplots showing the relationship between stygofauna taxon richness per sample and different physico-chemical variables; In Figure 10 the scatterplots presented are based on available data in the Queensland Subterranean Aquatic Fauna database where: depth to groundwater is available for 113 samples in meters below ground level (mbgl); electrical conductivity is available for 137 samples in microSiemens per centimetre (μS/cm); pH is available for 130 samples; and temperature is available for 77 samples in degrees Celsius (°C).
Figure 5 from: Glanville K, Schulz C, Tomlinson M, Butler D (2016) Biodiversity and biogeography of groundwater invertebrates in Queensland, Australia. Subterranean Biology 17: 55-76. https://doi.org/10.3897/subtbiol.17.7542
Figure 5 - Biogeography of described families in Queensland, Australia; In Figure 5 the total number of subregions a described family has been recorded inhabiting is indicated by numerical figures located to the right of the bars and the total number of samples is indicated by numerical figures located along the y-axis.
Figure 4 from: Glanville K, Schulz C, Tomlinson M, Butler D (2016) Biodiversity and biogeography of groundwater invertebrates in Queensland, Australia. Subterranean Biology 17: 55-76. https://doi.org/10.3897/subtbiol.17.7542
Figure 4 - Stygofauna discovery rates by lithology in Queensland, Australia; In Figure 4 the discovery rate of stygofauna is indicated by numerical figures located above the columns, the total number of samples is indicated by numerical figures located along the x-axis, and the average stygofauna discovery rate (28%) is plotted as a grey, dashed line.
Figure 8 from: Glanville K, Schulz C, Tomlinson M, Butler D (2016) Biodiversity and biogeography of groundwater invertebrates in Queensland, Australia. Subterranean Biology 17: 55-76. https://doi.org/10.3897/subtbiol.17.7542
Figure 8 - Distribution of described families across different lithologies in Queensland, Australia; In Figure 8 the total number of lithologies is indicated by numerical figures located to the right of the bars and the total number of samples is indicated by numerical figures located along the y-axis.
Figure 7 from: Glanville K, Schulz C, Tomlinson M, Butler D (2016) Biodiversity and biogeography of groundwater invertebrates in Queensland, Australia. Subterranean Biology 17: 55-76. https://doi.org/10.3897/subtbiol.17.7542
Figure 7 - Diversity of described families across different lithologies in Queensland, Australia; In Figure 7 the total number of described families is indicated by numerical figures located above the columns and the total number of samples is indicated by numerical figures located along the x-axis.
Figure 6 from: Glanville K, Schulz C, Tomlinson M, Butler D (2016) Biodiversity and biogeography of groundwater invertebrates in Queensland, Australia. Subterranean Biology 17: 55-76. https://doi.org/10.3897/subtbiol.17.7542
Figure 6 - Diversity of described families in different IBRA subregions in Queensland, Australia; In Figure 6 the total number of described families is indicated by numerical figures located to the right of the bars and the total number of samples is indicated by numerical figures located along the y-axis.
Figure 9 from: Glanville K, Schulz C, Tomlinson M, Butler D (2016) Biodiversity and biogeography of groundwater invertebrates in Queensland, Australia. Subterranean Biology 17: 55-76. https://doi.org/10.3897/subtbiol.17.7542
Figure 9 - Comparison of systemic composition of described families from Australia and the World Average; In Figure 9 the systemic composition of described stygofauna families is compared between the Pilbara region (Western Australia, Australia) derived from Eberhard et al. (2005), Queensland (Australia), and the World Average derived from Eberhard et al. (2005).
Figure 3 from: Glanville K, Schulz C, Tomlinson M, Butler D (2016) Biodiversity and biogeography of groundwater invertebrates in Queensland, Australia. Subterranean Biology 17: 55-76. https://doi.org/10.3897/subtbiol.17.7542
Figure 3 - Distribution of stygofauna sampling effort by lithology in Queensland, Australia; In Figure 3 the total number of samples is indicated by numerical figures located above the columns and the percentage of samples is indicated by numerical figures along the x-axis.
Figure 2 from: Glanville K, Schulz C, Tomlinson M, Butler D (2016) Biodiversity and biogeography of groundwater invertebrates in Queensland, Australia. Subterranean Biology 17: 55-76. https://doi.org/10.3897/subtbiol.17.7542
Figure 2 - Outline map of Queensland, Australia highlighting the location of stygofauna sampling sites and other localities; In Figure 2 an outline map shows the location of all 582 stygofauna sampling sites and other key localities mentioned in the text (e.g. Bowen Basin, Murray–Darling Basin, Proserpine–Sarina Lowlands IBRA region).
Figure 4 from: Souza Silva M, Ferreira RL (2016) The first two hotspots of subterranean biodiversity in South America. Subterranean Biology 19: 1-21. https://doi.org/10.3897/subtbiol.19.8207
Figure 4 - Species accumulation curves for the two Brazilian hotspots. The time-scale do not present regular intervals. Such curves were performed considering both data from literature and the new records here presented.
Figure 1 from: Souza Silva M, Ferreira RL (2016) The first two hotspots of subterranean biodiversity in South America. Subterranean Biology 19: 1-21. https://doi.org/10.3897/subtbiol.19.8207
Figure 1 - Areias cave system (F, G) in the Atlantic Rain Forest (C) and Toca do Gonçalo Cave (A, D, E) in Caatinga (B). Photos F and G by Daniel Menin.
Figure 3 from: Souza Silva M, Ferreira RL (2016) The first two hotspots of subterranean biodiversity in South America. Subterranean Biology 19: 1-21. https://doi.org/10.3897/subtbiol.19.8207
Figure 3 - Some of the stygobiotic and troglobitic species in Toca do Gonçalo. Rhandiopsis sp. n. (A), Spelaeogamarus trajanoae (B), Phalangopsidae sp. n. (C), Coarazuphium caatinga (D), Lygromma sp. n. (E), Scleropactidae sp. n. (F), Newportia spelaea (G), Clivinina sp. n. (H), Pongycarcinia xyphidiorus (I), Allokoenenia sp. n. (J), Rotadiscus sp. n. (K), Cthoniidae sp. n. (L), Geophilomorpha sp. n. (M), Nicoletiidae sp. n. (N).
Figure 2 from: Souza Silva M, Ferreira RL (2016) The first two hotspots of subterranean biodiversity in South America. Subterranean Biology 19: 1-21. https://doi.org/10.3897/subtbiol.19.8207
Figure 2 - Some of the stygobiotic and troglobitic species in Areias cave system, São Paulo, Brazil. Pimelodella kronei (A), Pachylospeleus strinatii (B), Pseudochthonius strinatii (C), Ideoroncus cavicola (D), Pselaphidae sp. n. (E), Spelaeobochica muchmorei (F), Hahniidae sp. n. (G) Cryptodesmus spn (H), Schizogenius ocelatus (I), Cryptops iporangensis (J), Potamolithus troglobius (K), Crypturodesmus spn (L), Leodesmus yporangae (M), Hyallela epikarstica (N), Aegla cavernicola (O), Peridontodesmella sp. (P).
Figure 3 from: García R, Andújar C, Oromí P, López H (2020) Oromia orahan (Curculionidae, Molytinae), a new subterranean species for the Canarian underground biodiversity. Subterranean Biology 35: 1-14. https://doi.org/10.3897/subtbiol.35.52583
Figure 3 Appearance of mud/dirt covered (A) and clean (B) individuals of Oromia orahan sp. nov.
Figure 1 from: García R, Andújar C, Oromí P, López H (2020) Oromia orahan (Curculionidae, Molytinae), a new subterranean species for the Canarian underground biodiversity. Subterranean Biology 35: 1-14. https://doi.org/10.3897/subtbiol.35.52583
Figure 1 Habitus of Oromia orahan sp. nov. (female) in dorsal and lateral view.
Supplementary material 1 from: Fernandez D, Millán A, Rizzo V, Comas J, Lleopard E, Pastor J, Pallarés S, Abellán P, Spada M, Bilton DT, Ribera I (2018) The CAVEheAT project: climate change, thermal niche and conservation of subterranean biodiversity. ARPHA Conference Abstracts 1: e30105. https://doi.org/10.3897/aca.1.e30105
The CAVEheATproject: climate change, thermal niche and conservation of subterranean biodiversity
Figure 1 from: Glanville K, Schulz C, Tomlinson M, Butler D (2016) Biodiversity and biogeography of groundwater invertebrates in Queensland, Australia. Subterranean Biology 17: 55-76. https://doi.org/10.3897/subtbiol.17.7542
Figure 1 - Diagram map of the structure of the 'Queensland Subterranean Aquatic Fauna Database'.
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Allen Brain Atlas
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