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676 results for “Manis”
Figure 2 in How many species of Hipposideros have occurred on Madagascar since the Late Pleistocene?
Figure 2. Maximum likelihood phylogeny inferred from analysis of Hipposideros commersoni cytochrome b data. Bayesian posterior probability (bold) and maximum likelihood bootstrap values are provided and only values greater than 0.50 and 50, respectively, are shown. For further details on the sequenced specimens see Table S2.
Figure 6 in How many species of Hipposideros have occurred on Madagascar since the Late Pleistocene?
Figure 6. Different views of skull and mandible of neotype of Hipposideros commersoni (FMNH 175972, female) from Province de Fianarantsoa, Parc National de l'Isalo, along Sahanafa River. Dorsal view of cranium (upper row, left), ventral view of cranium (upper row, right), and lateral view of cranium and mandible (lower row). (Photographs taken by J. Weinstein, Field Museum image number Z95239_007d.)
Figure 1 in How many species of Hipposideros have occurred on Madagascar since the Late Pleistocene?
Figure 1. Map of Madagascar showing different sampling localities of Hipposideros used in the morphological and molecular parts of this study and the different clade representation. The map also shows other localities mentioned in the text. An overlay is used of the simplified bioclimatic regions of the island (Cornet, 1974).
FIGURE 5. Syngonanthus polyaxis. A. Branched stem with many leaf rosettes and primary axis. B in Novelties from the Serra Nova State Park (Minas Gerais, Brazil): two new endemic species of Eriocaulaceae
FIGURE 5. Syngonanthus polyaxis. A. Branched stem with many leaf rosettes and primary axis. B. Primary axis (below) with verticillate apical bracts and secondary axis (above). C. Whorled bracts of primary axis and four emerging secondary axes. D. Verticillate bracts of secondary axis, spathes, scapes and young capitula. E. Scapes in lax umbel. F. Capitulum with exserted staminate flower at anthesis. G. Habit, showing one individual with multiple synflorescences. H. Habitat. Photos by Livia Echternacht.
Data from: SNF1-related protein kinase 1: the many-faced signaling hub regulating developmental plasticity in plants
<p>The Snf1-Related Protein Kinase 1 (SnRK1) is the plant homolog of the heterotrimeric AMP-activated Protein Kinase/ Sucrose Non-Fermenting 1 (AMPK/Snf1), which works as a major regulator of growth under nutrient-limiting conditions in eukaryotes. Along with its conserved role as a master regulator of sugar starvation responses, SnRK1 is involved in controlling the developmental plasticity and resilience under diverse environmental conditions in plants. In this review, through mining and analyzing the interactome and phosphoproteome data of SnRK1, we are highlighting its role in fundamental cellular processes such as gene regulation, protein synthesis, primary metabolism, protein trafficking, nutrient homeostasis, autophagy, etc. Along with the well-characterized molecular interaction in SnRK1 signaling, our analysis highlights several unchartered regions of SnRK1 signaling in plants such as its possible communication with chromatin remodelers, histone modifiers, inositol phosphate signaling, etc. We also discuss potential reciprocal interactions of SnRK1 signaling with other signaling pathways and cellular processes, which could be involved in maintaining flexibility and homeostasis under different environmental conditions. Overall, this review provides a comprehensive overview of the SnRK1 signaling network in plants and suggests many novel directions for future research.</p>
FIGURE 41 in Taxonomy of spatially disjunct alpine Teleiopsis albifemorella s. lat. (Lepidoptera: Gelechiidae) revealed by molecular data and morphology — how many species are there?
FIGURE 41. Maximum Likelihood tree of the Teleiopsis based on concatenated data of COI, CAD, EF-1a, IDH, MDH and wingless genes. The tree was rooted on Carpatolechia notatella (not depicted because of very long branch leading to it). Bootstrap support values for T. albifemorella and T. paulheberti are shown below the nodes.
FIGURES 29–32 in Taxonomy of spatially disjunct alpine Teleiopsis albifemorella s. lat. (Lepidoptera: Gelechiidae) revealed by molecular data and morphology — how many species are there?
FIGURES 29–32. Female genitalia of Teleiopsis paulheberti sp. nov., segment VIII and antrum. 29, paratype, Italy (Cuneo), slide GEL 1162; 30, paratype, France (Alpes-Maritimes), slide GEL 1161; 31, paratype, France (Hautes-Alpes), slide GEL 1171; 32, as 31, diagnostic details of antrum.
FIGURE 40 in Taxonomy of spatially disjunct alpine Teleiopsis albifemorella s. lat. (Lepidoptera: Gelechiidae) revealed by molecular data and morphology — how many species are there?
FIGURE 40. Neighbor-joining trees of the Teleiopsis (implemented under Kimura 2 Parameter model) of nuclear genes CAD, EF-1a, IDH, MDH and wingless.
FIGURE 39 in Taxonomy of spatially disjunct alpine Teleiopsis albifemorella s. lat. (Lepidoptera: Gelechiidae) revealed by molecular data and morphology — how many species are there?
FIGURE 39. Neighbor-joining tree of the Teleiopsis (implemented under Kimura 2 Parameter model) based on sequences of the mtDNA COI gene 5' fragment (DNA barcode, 658 bp). Bootstrap support values, based on 500 pseudoreplicates, are shown for internal nodes. The tree was rooted on T. terebinthinella, the presumed sister taxon of other species. The scale bar indicates 0.5% change in sequence composition.
FIGURES 33–38 in Taxonomy of spatially disjunct alpine Teleiopsis albifemorella s. lat. (Lepidoptera: Gelechiidae) revealed by molecular data and morphology — how many species are there?
FIGURES 33–38. Female genitalia of Teleiopsis albifemorella, details of signum. 33–35, T. albifemorella: 33, Austria (North Tyrol), slide GEL 1165; 34, Austria (Upper Austria), slide GEL 1168; 35, Slovenia, slide GEL 1164. 36–38, T. paulheberti sp. nov.: 36, paratype, Italy (Cuneo), slide GEL 1162; 37, paratype, France (Alpes-Maritimes), slide GEL 1161; 38, paratype, France (Hautes-Alpes), slide GEL 1171.
FIGURES 7–10 in Taxonomy of spatially disjunct alpine Teleiopsis albifemorella s. lat. (Lepidoptera: Gelechiidae) revealed by molecular data and morphology — how many species are there?
FIGURES 7–10. Adults of Teleiopsis paulheberti sp. nov., males. 7, paratype, Italy (Cuneo); 8, paratype, Italy (L´Aquila); 9, paratype, France (Alpes-Maritimes); 10, paratype France (Hautes-Alpes).
FIGURES 25–28 in Taxonomy of spatially disjunct alpine Teleiopsis albifemorella s. lat. (Lepidoptera: Gelechiidae) revealed by molecular data and morphology — how many species are there?
FIGURES 25–28. Female genitalia of Teleiopsis albifemorella, segment VIII and antrum. 25, Austria (North Tyrol), slide GEL 1165; 26, Austria (Upper Austria), slide GEL 1168; 27, Slovenia, slide GEL 1164; 28, as 25, diagnostic details of antrum.
FIGURES 19–24 in Taxonomy of spatially disjunct alpine Teleiopsis albifemorella s. lat. (Lepidoptera: Gelechiidae) revealed by molecular data and morphology — how many species are there?
FIGURES 19–24. Segment VIII of male Teleiopsis. 19–21, T. albifemorella: 19, Austria (North Tyrol), slide GEL 1166; 20, Austria (Upper Austria), slide GEL 1167; 21, Slovenia, slide GEL 1163. 22–24, T. paulheberti sp. nov.: 22, holotype, Italy (Cuneo), slide GEL 1159; 23, paratype, Italy (L´Aquila), slide GEL 1169; 24, paratype, France (Hautes-Alpes), slide GEL 1172.
FIGURES 15–18 in Taxonomy of spatially disjunct alpine Teleiopsis albifemorella s. lat. (Lepidoptera: Gelechiidae) revealed by molecular data and morphology — how many species are there?
FIGURES 15–18. Male genitalia of Teleiopsis paulheberti sp. nov. 15, holotype, Italy (Cuneo), slide GEL 1159; 16, paratype, Italy (L´Aquila), slide GEL 1169; 17, paratype, France (Hautes-Alpes), slide GEL 1172; 18, as 17, diagnostic details of uncusgnathos region.
FIGURES 1–6 in Taxonomy of spatially disjunct alpine Teleiopsis albifemorella s. lat. (Lepidoptera: Gelechiidae) revealed by molecular data and morphology — how many species are there?
FIGURES 1–6. Adults of Teleiopsis albifemorella, males. 1–2, Austria (North Tyrol); 3, Austria (Upper Austria); 4, Italy (Udine); 5, Italy (South Tyrol); 6, Italy (Verona).
FIGURES 11–14 in Taxonomy of spatially disjunct alpine Teleiopsis albifemorella s. lat. (Lepidoptera: Gelechiidae) revealed by molecular data and morphology — how many species are there?
FIGURES 11–14. Male genitalia of Teleiopsis albifemorella. 11, Austria (North Tyrol), slide GEL 1166; 12, Austria (Upper Austria), slide GEL 1167; 13, Slovenia, slide GEL 1163; 14, as 13, diagnostic details of uncus-gnathos region.
Analysis of the nonlinear optical response of excitons in type-I and type-II quantum wells including many-body correlations
<p>Dataset of the publication “Analysis of the nonlinear optical response of excitons in type-I and type-II quantum wells including many-body correlations”, A. Trautmann, M. Stein, F. Schäfer, D. Anders, C. Ngo, J. T. Steiner, M. Reichelt, S. Chatterjee, and T. Meier, Proc. SPIE 12419, Ultrafast Phenomena and Nanophotonics XXVII, 124190A (2023) ( <a href="https://doi.org/10.1117/12.2650169">https://doi.org/10.1117/12.2650169</a> ). The zip file includes the data on which the plots are based.</p>
FIGURE 7. Pleurosicya micheli. A in How many valid Pleurosicya (Teleostei: Gobiidae) species are known from the Red Sea?
FIGURE 7. Pleurosicya micheli. A: 22.0 mm SL, Maricaban I., Philippines; B: Anilao, Philippines; C: Sulawesi, Indonesia; D: Papua New Guinea. Photos by J.T. Williams (A), A. Ryanskiy (B–D).
FIGURE 6. Pleurosicya mossambica. A in How many valid Pleurosicya (Teleostei: Gobiidae) species are known from the Red Sea?
FIGURE 6. Pleurosicya mossambica. A: ROM 60057, 19.8 mm SL, Moheli I., Comoros Isl.; B: ROM 58028, 16.4 mm SL, Chagos Archipelago; C: Maldives. Pleurosicya cf. mossambica. D: ROM 74851, 16.0 mm SL, Palau. Photos by R. Winterbottom (A, B & D), A. Ryanskiy (C).
FIGURE 5. Pleurosicya mossambica, Red Sea. A in How many valid Pleurosicya (Teleostei: Gobiidae) species are known from the Red Sea?
FIGURE 5. Pleurosicya mossambica, Red Sea. A: Mangrove Bay, Al Quseir, 14 m depth; B: Marsa Shagra, Marsa Alam, 7 m depth; C: Dahab, Egypt, 8 m depth; D: Dahab, Egypt, 12 m depth. Photos by S.V. Bogorodsky.
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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.