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FIGURE 1. A in Distinguishing between three modern Ellobius species (Rodentia, Mammalia) and identification of fossil Ellobius from Kaldar Cave (Iran) using geometric morphometric analyses of the first lower molar
FIGURE 1. A) Occlusal surface of Ellobius right lower m1: triangle (T); buccal re-entrant angle (BRA); lingual reentrant angle (LRA); anterior cap (AC); posterior lobe (PL); B) Lingual view of left lower m1.
FIGURE 5 in Distinguishing between three modern Ellobius species (Rodentia, Mammalia) and identification of fossil Ellobius from Kaldar Cave (Iran) using geometric morphometric analyses of the first lower molar
FIGURE 5. Principal component analysis on the normalized landmarks and sliding semilandmarks and shape configuration at the extreme ends of the two first PCs.
FIGURE 7 in Distinguishing between three modern Ellobius species (Rodentia, Mammalia) and identification of fossil Ellobius from Kaldar Cave (Iran) using geometric morphometric analyses of the first lower molar
FIGURE 7. Morphological differences between Ellobius fuscocapillus (left) and Ellobius lutescens (right). Arrows depict the displacements between corresponding landmarks in the reference (dots) and Ellobius lutescens as target specimens.
Stable isotopes and radiocarbon dating results on Late Pleistocene red deer and horse from the Serinyà caves (Girona, Catalonia, Spain)
<p>Table 1: Minimum (Min), maximum (Max), mean and standard-deviations (SD) of <em>δ</em><sup>13</sup>C<sub>carb</sub> and <em>δ</em><sup>18</sup>O<sub>carb</sub> values per horse and red deer tooth. Numbers in bold indicate isotopic values corresponding to peaks (summer) or troughs (winter) detected from clear sinusoidal patterns in <em>δ</em><sup>18</sup>O<sub>carb</sub> values. Numbers in bold correspond to minimum and maximum values in teeth revealing a sinusoidal pattern. LM3 and UM3 stand for lower third molar and upper third molar, respectively. LM2 stands for lower second molar. R is for the right side, L is for the left side. N: number of analyses.</p> <p>Table 2: Minimum, maximum, mean and standard-deviations of <em>δ</em><sup>13</sup>C<sub>coll</sub>, <em>δ</em><sup>15</sup>N<sub>coll</sub> for horse and red deer per technocomplex phases. na stands for not applicable. N: number of samples.</p> <p>Table A.1: Detailed isotopic results (<em>δ</em><sup>13</sup>C<sub>carb</sub> and <em>δ</em><sup>18</sup>O<sub>carb</sub>) for horse teeth with incremental sampling. Underlined numbers correspond to outlier data. Brackets are added around isotopic values that are not considered for further interpretation. R stands for the right side, L is for the left side.</p> <p>Table A.2: Detailed isotopic results (<em>δ</em><sup>13</sup>C<sub>carb</sub> and <em>δ</em><sup>18</sup>O<sub>carb</sub>) for red deer teeth with incremental sampling. Underlined numbers correspond to outlier data. Brackets are added around isotopic values that are not considered reliable for further interpretation. R is for the right side, L is for the left side.</p> <p>Table A.3: Results of elemental analysis on bone or dentine (N<sub>bone or dentine</sub>) and collagen (C<sub>coll</sub>, N<sub>coll</sub>, C:N<sub>coll</sub>) and of isotopic analysis on collagen (<em>δ</em><sup>13</sup>C<sub>coll</sub>, <em>δ</em><sup>15</sup>N<sub>coll</sub>) from horse (<em>Equus ferus</em>), red deer (<em>Cervus elaphus</em>) at the Serinyà caves. Underlined numbers correspond to outlier data. Brackets are added around isotopic values that are not considered reliable for further interpretation. R is for the right side, L is for the left side. * species determination confirmed by ZooMS analysis. Tüb. stands for Tübingen and NU for National University.</p> <p>Table A.4: Results of elemental analysis on bone or dentine (N<sub>bone or dentine</sub>) and collagen (C<sub>coll</sub>, N<sub>coll</sub>, C:N<sub>coll</sub>) and of isotopic analysis on collagen (<em>δ</em><sup>13</sup>C<sub>coll</sub>, <em>δ</em><sup>15</sup>N<sub>coll</sub>) from large bovids (<em>Bos/Bison</em>) and muskox (<em>Ovibos moschatus</em>) at the Serinyà caves. Underlined numbers correspond to outlier data. Brackets are added around isotopic values that are not considered reliable for further interpretation. R is for the right side, L is for the left side. * species determination confirmed by ZooMS analysis. Tüb. stands for Tübingen.</p> <p>Table A.5: Results of elemental analysis on collagen (C<sub>coll</sub>, N<sub>coll</sub>, C:N<sub>coll</sub>) and of isotopic analysis on collagen (<em>δ</em><sup>13</sup>C<sub>coll</sub>,<em>δ</em><sup>15</sup>N<sub>coll</sub>) and radiocarbon dates (<sup>14</sup>C) from horse (<em>Equus ferus</em>), red deer (<em>Cervus elaphus</em>), reindeer (<em>Rangifer tarandus</em>), muskox (<em>Ovibos moschatus</em>), rabbit (<em>Oryctolagus cuniculus</em>) and human (<em>Homo sapiens</em>) at the Serinyà caves. R is for the right side, L is for the left side. * species determination confirmed by ZooMS analysis. na stands for not applicable, nd for not determined and ind for indetermined.</p>
Data for: Summer declines of cave-dwelling Tricolored Bats
<p>Several bat species experienced rapid population declines in the northern United States and Canada in response to the white-nose syndrome (WNS) epizootic. The pathogen has since spread across the United States, including the southeast, where relatively warm temperatures may change host–pathogen interactions. In the cave-rich Tennessee-Alabama-Georgia (TAG) region, we examined the impacts of WNS and forest cover on the Tricolored Bat (<em>Perimyotis subflavus</em>) metapopulation using a long-term dataset of 832 cave surveys conducted in summer and winter from 2004–2022. Most bat colonies were small (<30 individuals), and bats were more likely to be present and abundant in caves surrounded by high percent forest cover, reiterating the importance of forest management for bat conservation. When comparing the years before and after the pathogen arrived in 2010–2012, bat presence and abundance during winter hibernation did not change. This stability contrasts significant declines in other studies, suggesting that Tricolored Bat populations respond differently to WNS in small colonies in the TAG region. Fewer Tricolored Bats used caves in the summer than during hibernation, but across all years, we observed 1021 Tricolored Bats in 121 caves during summer surveys. Unlike stable winter trends, bat presence and abundance declined in the post-WNS period in summer, when cave use is optional. This first broad geographical analysis of summer cave use highlights a potentially important change in bat behavior. Disease surveillance and conservation efforts that target caves with relatively small Tricolored Bat colonies in winter and/or summer may be important for regional population persistence of this threatened species.</p>
Fig. 9 in New giant genus of Parabathynellidae (Crustacea: Bathynellacea): first record of Bathynellacea in an Australian cave
Fig. 9. Male ThVIII of different species from Australia. A. Arkaroolabathynella bispinosa Abrams & King, 2013. B. Notobathynella octocamura Camacho & Hancock, 2011. C. Lockyerenella danschmidti Camacho & Little, 2017. D. Brevisomabathynella cooperi Cho, Park & Ranga Reddy, 2006. E. Billibathynella wolfrannodti Hong & Cho, 2009. F. Megabathynella totemensis Camacho & Abrams gen. et sp. nov. G. Octobathynella peelensis Camacho & Hancock, 2010. Original and redrawings by AIC. Scale bars in mm.
Fig. 8 in New giant genus of Parabathynellidae (Crustacea: Bathynellacea): first record of Bathynellacea in an Australian cave
Fig. 8. Megabathynella totemensis Camacho & Abrams gen. et sp. nov., holotype, ♂ (NTM Cr19141), microscope photographs. A. ThVIII (latero external view). B–E, G–J. Details of ThVIII. F. ThVIII (latero internal view).
Fig. 7 in New giant genus of Parabathynellidae (Crustacea: Bathynellacea): first record of Bathynellacea in an Australian cave
Fig. 7. Megabathynella totemensis Camacho & Abrams gen. et sp. nov., holotype, ♂ (NTM Cr19141), microscope photographs. A. ThI. B. ThI details. C. ThIII. D. Details of basipod and epipod of ThV. E. ThV. F. Furca and uropod. G. Exopod and endopod of uropod. Scale bar in mm.
Fig. 6 in New giant genus of Parabathynellidae (Crustacea: Bathynellacea): first record of Bathynellacea in an Australian cave
Fig. 6. Megabathynella totemensis Camacho & Abrams gen. et sp. nov., holotype, ♂ (NTM Cr19141), microscope photographs. A. AI. B. AII. C. Labrum. D. Md. E. Md. F. Mandibular palp. G. MxI. H. MxI. I. MxII. Scale bars in mm.
Fig. 10 in New giant genus of Parabathynellidae (Crustacea: Bathynellacea): first record of Bathynellacea in an Australian cave
Fig. 10. Male ThVIII of different species from Asia. A. Paraeobathynella vietnamensis Camacho, 2005. B. Sketinella trontelji Camacho, 2005. C. Kampucheabathynella Cho, Kry & Chhenh, 2015. D. Sinobathynella decamera Camacho, Trontelj & Zagmajster 2006. E. Allobathynella coreana Morimoto, 1970. Original and redrawing by AIC. Scale bar in mm.
Fig. 5 in New giant genus of Parabathynellidae (Crustacea: Bathynellacea): first record of Bathynellacea in an Australian cave
Fig. 5. Megabathynella totemensis Camacho & Abrams gen. et sp. nov. A–B. Holotype, ♂ (NTM Cr19141). A. Thoracopod VIII (latero-external view). B. Thoracopod VIII (latero-internal view). C–F. Allotype, ♀ (NTMCr19142). C. ThVIII. D. Sympod of uropod (dorsal view). E. Exopod and endopod of the uropod (dorsal view). F. Furca (dorsal view). Scale bars in mm.
Fig. 2 in New giant genus of Parabathynellidae (Crustacea: Bathynellacea): first record of Bathynellacea in an Australian cave
Fig. 2. Habitus of female Megabathynella totemensis Camacho & Abrams gen. et sp. nov., paratype (WAM C73466J).
Fig. 4 in New giant genus of Parabathynellidae (Crustacea: Bathynellacea): first record of Bathynellacea in an Australian cave
Fig. 4. Megabathynella totemensis Camacho & Abrams gen. et sp. nov. A. Holotype, ♂ (NTM Cr19141) thoracopod I. B. Allotype, ♀ (NTM Cr19142), thoracopod I. C–D. Last article of endopod of ThVII of two male paratypes (WAMC73466H and MNCN 20.04/20931). Scale bar in mm.
Fig. 3 in New giant genus of Parabathynellidae (Crustacea: Bathynellacea): first record of Bathynellacea in an Australian cave
Fig. 3. Megabathynella totemensis Camacho & Abrams gen. et sp. nov. A–C, G–K. Holotype, ♂ (NTM Cr19141). A. Antennule (dorsal view). B. Antenna (dorsal view). C. Labrum. D–E. Paratype, ♀ (MNCN20.04/20932). D. Labrum. E. Mandible. F. Allotype, ♀ (NTM Cr19142), mandibular palp of female. G. Maxillule. H. Maxilla. I. Plumose seta of the first articles of AI. J. Article three of AI. K. Article eight of AI, with special plumose seta and two aesthetascs. Scale bars in mm.
Fig. 1 in New giant genus of Parabathynellidae (Crustacea: Bathynellacea): first record of Bathynellacea in an Australian cave
Fig. 1. Habitus of male Megabathynella totemensis Camacho & Abrams gen. et sp. nov., paratype (WAM C73466H).
Fig. 13 in Biological response to geochemical and hydrological processes in a shallow submarine cave
Fig. 13: The effect of hydrodynamics inside the Y-Cave, the location behind section B-B' (Fig. 2) at 5.5 m of depth, where the unusually coloured sediment sample was collected for analysis.
Fig. 12 in Biological response to geochemical and hydrological processes in a shallow submarine cave
Fig. 12: Limestone tablets from the three representative sites after the 1-year exposure period: A) with bioaccumulation at site 1; B) corroded at site 3; C) abraded at site 6 (Fig. 3, Tab. 1).
Fig. 11 in Biological response to geochemical and hydrological processes in a shallow submarine cave
Fig. 11: Cave features: A) stalactites in the chamber with the air pocket (section C-C'); B) submerged stalagmites and flowstones with a lack of marine cave biota (section C-C'); C) submerged scallops (asymmetrical, cuspate, oyster-shell-shaped dissolution depressions in the cave walls used as an indicator of flow direction; Murphy, 2012), (section D-D'); D) corroded cave walls (section F-F').
Fig. 5 in Biological response to geochemical and hydrological processes in a shallow submarine cave
Fig. 5: The annual variation of temperature along the Y-Cave (from August 23–27, 2003 to July 4/October 8, 2004). Measurement positions are given in Fig. 3 and depths in Table 1.
Fig. 10 in Biological response to geochemical and hydrological processes in a shallow submarine cave
Fig. 10: The mass (m.f.) and volume fractions (v.f.) of four sediment categories in the sediment sample collected behind section B-B' (Fig. 2), at 5.5 m of depth inside the Y-Cave; A) detrital terrigenous sediment>4 mm, B) mixed biogenic and terrigenous detritus, C) shells of gastropod Homalopoma sanguineum, D) other biogenic material – shells, tests and skeletons of other marine organisms.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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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
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