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FIGURE 4 in Description of a new subterranean breeding brown frog (Ranidae: Rana) from Japan
FIGURE 4. Histogram of adult SVL (mm) of two Rana species. A: histogram for males in total; B–D: separated histograms of males of mt-lineages A-1b, A-1a, and B-2a, respectively; and E: females in total.
FIGURE 8 in New insights into the subterranean genus Speoplanes Müller, 1911 (Coleoptera, Leiodidae, Cholevinae) from the Dinarides
FIGURE 8. Metatergal apparatus (A) and metendosternite (B) of S. giganteus: male, Mosor, Ledenica pod Jabukovcem.
FIGURE 7 in New insights into the subterranean genus Speoplanes Müller, 1911 (Coleoptera, Leiodidae, Cholevinae) from the Dinarides
FIGURE 7. Female genitalia of Speoplanes sp. On the left: S. giganteus, Mosor, Ledenica pod Jabukovcem, spermatheca, mediotergite and stylus; on the right: S. biocovensis, Biokovo, Jama ispod Sv. Jure, spermatheca, mediotergite and stylus.
FIGURE 6 in New insights into the subterranean genus Speoplanes Müller, 1911 (Coleoptera, Leiodidae, Cholevinae) from the Dinarides
FIGURE 6. Speoplanes sp., parameres of the male genitalia. A: Apical region of left paramere. Left: S. giganteus, Mosor, Ledenica pod Jabukovcem, right: S. biocovensis, Biokovo, Jama ispod Sv. Jure. B: Apical region of right paramere. Left: S. giganteus, Mosor, Jama Velika Gajna, right: S. biocovensis, Mali Šibenik, Jama na vrhu Malog Šibenika.
FIGURE 5 in New insights into the subterranean genus Speoplanes Müller, 1911 (Coleoptera, Leiodidae, Cholevinae) from the Dinarides
FIGURE 5. Morphological variation of the mesoventral carina of Speoplanes species. A: Mesoventral carina of S. giganteus male (left: specimen of Mosor, Ledenica pod Jabukovcem, right: Mosor, Jama Velika Gajna). B: Mesoventral carina of S. biocovensis male (left: specimen of Mali Šibenik, Jama na vrhu Malog Šibenika; right: Biokovo, Jama ispod Sv. Jure).
FIGURE 3 in New insights into the subterranean genus Speoplanes Müller, 1911 (Coleoptera, Leiodidae, Cholevinae) from the Dinarides
FIGURE 3. Species differentiation for females of Speoplanes. Speoplanes giganteus (A) has longer protibia and metatibia compared to the length of head-pronotum and elytra respectively, whereas Speoplanes biocovensis (B) has protibia and metatibia of equal length to head-pronotum and elytra respectively.
FIGURE 1 in New insights into the subterranean genus Speoplanes Müller, 1911 (Coleoptera, Leiodidae, Cholevinae) from the Dinarides
FIGURE 1. Bayesian phylogenetic reconstruction of Speoplanes based on 28S and COX1 genes. Speoplanes giganteus is coloured in blue, Speoplanes biocovensis in green. Labels on branches represent posterior probabilities and bootstrap values.
FIGURE 2 in New insights into the subterranean genus Speoplanes Müller, 1911 (Coleoptera, Leiodidae, Cholevinae) from the Dinarides
FIGURE 2. Habitus of the Speoplanes species. Male (right) and female (left) habitus of Speoplanes giganteus (A) and Speoplanes biocovensis (B)
Supplementary material 5 from: Royzenblat S, Kulacic J, Friedrich M (2023) Evidence of ancestral nocturnality, locomotor clock regression, and cave zone-adjusted sleep duration modes in a cave beetle. Subterranean Biology 45: 79-94. https://doi.org/10.3897/subtbiol.45.100717
Activity stats comparisons of monitor-adjusted LD animals in D phase with monitor-adjusted DD animals
Development of microsatellite markers for colony delineation of the invasive Asian subterranean termite in South Florida and Taiwan
<p>Delineating the colony identity of <em>Coptotermes gestroi </em>(Wasmann) is a core issue of colony elimination in the implementation of subterranean termite baiting systems. Invasion history is believed the possible cause of genetic variabilities among colonies. Haplotype network analysis of mitochondrial cytochrome <em>c</em> oxidase subunit II revealed the multiple origins of American <em>C</em>.<em> gestroi</em> from<em> </em>the Philippines and Southeast Asia and the Taiwan population only from the Philippines. We further developed 21 new microsatellite markers for the comparison of genetic variabilities on colony delineation of <em>C</em>.<em> gestroi </em>colonies from South Florida (invaded ~30 years; 3–7 generations) and Taiwan (~110 years; 13–27 generations). The present microsatellite markers with 1–4 alleles per locus have validated the effectiveness of colony delineation for three incipient colonies reared in the laboratory and three field colonies from Taiwan. Genetic admixture of the Floridian <em>C</em>. <em>gestroi</em> probably caused by recent invasion history, multiple invasions, and anthropogenic activities among regions. A possible introduction event likely occurred through human-mediated activities between Fort Lauderdale and Miami. Overall, these new microsatellite markers provide suitable and efficient candidate genetic markers for colony delineation of <em>C</em>. <em>gestroi</em> to consolidate the effectiveness of the colony elimination system in termite management.</p>
Supplementary material 3 from: Miranda-Gamboa R, Espinasa L, Verde-Ramírez MA, Hernández-Lozano J, Lacaille JL, Espinasa M, Ornelas-García CP (2023) A new cave population of Astyanax mexicanus from Northern Sierra de El Abra, Tamaulipas, Mexico. Subterranean Biology 45: 95-117. https://doi.org/10.3897/subtbiol.45.98434
Contrasting vertical isolation between Pachón and El Refugio caves and the fossil canyon between Pachón and El Refugio caves
Supplementary material 2 from: Miranda-Gamboa R, Espinasa L, Verde-Ramírez MA, Hernández-Lozano J, Lacaille JL, Espinasa M, Ornelas-García CP (2023) A new cave population of Astyanax mexicanus from Northern Sierra de El Abra, Tamaulipas, Mexico. Subterranean Biology 45: 95-117. https://doi.org/10.3897/subtbiol.45.98434
Geometric morphometric coordinates, PCA values obtained from the geometric morphometric data and orbit diameter values for the populations
Supplementary material 4 from: Eusébio RP, Fonseca PE, Rebelo R, Mathias ML, Reboleira ASPS (2023) How to map potential mesovoid shallow substratum (MSS) habitats? A case study in colluvial MSS. Subterranean Biology 45: 141-156. https://doi.org/10.3897/subtbiol.45.96332
Abundance of invertebrates collected in colluvial Mesovoid Shallow Substratum (MSS) at the Arrábida National Park
Supplementary material 3 from: Eusébio RP, Fonseca PE, Rebelo R, Mathias ML, Reboleira ASPS (2023) How to map potential mesovoid shallow substratum (MSS) habitats? A case study in colluvial MSS. Subterranean Biology 45: 141-156. https://doi.org/10.3897/subtbiol.45.96332
Results of criteria met for each location pinpointed as potential colluvial Mesovoid Shallow Substratum (MSS)
Supplementary material 1 from: Eusébio RP, Fonseca PE, Rebelo R, Mathias ML, Reboleira ASPS (2023) How to map potential mesovoid shallow substratum (MSS) habitats? A case study in colluvial MSS. Subterranean Biology 45: 141-156. https://doi.org/10.3897/subtbiol.45.96332
Characterization of each of the locations found in situ as colluvial Mesovoid Shallow Substratum (MSS): latitude, longitude and estimated area (m2)
Supplementary material 5 from: Eusébio RP, Fonseca PE, Rebelo R, Mathias ML, Reboleira ASPS (2023) How to map potential mesovoid shallow substratum (MSS) habitats? A case study in colluvial MSS. Subterranean Biology 45: 141-156. https://doi.org/10.3897/subtbiol.45.96332
Total invertebrate abundance, collected in colluvial Mesovoid Shallow Substratum (MSS) at the Arrábida National Park
FIGURE 1 in A new species of the genus Pseudocrangonyx (Crustacea: Amphipoda: Pseudocrangonyctidae) from subterranean waters of Japan
FIGURE 1. Habitat and live specimen of Pseudocrangonys asuwaensis sp. nov. A, entrance of Nanatsuoguchi, Mt. Asuwa, Fukui, Japan; B, female (about 6 mm in body length).
FIGURE 4 in A new species of the genus Pseudocrangonyx (Crustacea: Amphipoda: Pseudocrangonyctidae) from subterranean waters of Japan
FIGURE 4. Pseudocrangonys asuwaensis sp. nov. holotype female (KUZ Z4464), 5.4 mm, Nanatsuoguchi, Mt. Asuwa, Fukui, Japan. A, pereopod 3, lateral view; B, dactylus of pereopod 3, lateral view; C–F, pereopods 4–7, lateral views.
FIGURE 5 in A new species of the genus Pseudocrangonyx (Crustacea: Amphipoda: Pseudocrangonyctidae) from subterranean waters of Japan
FIGURE 5. Pseudocrangonys asuwaensis sp. nov. holotype female (KUZ Z4464), 5.4 mm, Nanatsuoguchi, Mt. Asuwa, Fukui, Japan. A–C, epimeral plates 1–3, lateral views; D, pleopod 1, medial view; E, retinacula on peduncle of pleopod 1, medial view; F–H, uropods 1–3, dorsal views; I, telson, dorsal view.
FIGURE 7 in A new species of the genus Pseudocrangonyx (Crustacea: Amphipoda: Pseudocrangonyctidae) from subterranean waters of Japan
FIGURE 7. Maximum likelihood (ML) tree for 2922 bp of nuclear 28S and H3, and mitochondrial COI and 16S markers. Inset shows the full ML tree. The ML tree was constrained with the monophyly of the pseudocrangonyctid species, and two crangonyctid species, respectively. Numbers on nodes indicate bootstrap (BS) values for maximum likelihood ≥ 50% and Bayesian posterior probabilities (PP) ≥ 0.90. An asterisk denotes the node with BS ≥ 90%, PP ≥ 0.99.
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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.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
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.
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.