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676 results for “Manis”
Fig. 5 in There's gold in them thar hills! Morphology and molecules delimit species in Xerochrysum (Asteraceae; Gnaphalieae) and reveal many new taxa
Fig. 5. Semi-strong hybrid multi-dimensional scaling ordinations of morphological characters on subsets of species and putative entities of Xerochrysum representing broad distribution patterns across Australia (Table 4). (a) Northern; (b) southern; (c) eastern; (d) western. Each ball represents an individual sample, coloured by species or putative entity.
Fig. 3 in There's gold in them thar hills! Morphology and molecules delimit species in Xerochrysum (Asteraceae; Gnaphalieae) and reveal many new taxa
Fig. 3. Indumentum variation among species of Xerochrysum. White arrows indicate stipitate glands in a–g. Leaf surface: (a–c) adaxial; (d–g) abaxial. (a) Hispidulous and with glands (X. bracteatum sens. str., T.L.Collins 1005); (b) hispid and with glands (X. sp. Barrington Tops, T.L.Collins 1046); (c) hirsute to pilose, and with glands (X. sp. Point Lookout, T.L.Collins 958); (d) with glands (X. bracteatum sens. str., T.L.Collins 1005); (e) hirsute and with glands (X. sp. Barrington Tops, T.L.Collins 1046); (f) pilose and with glands (X. sp. Point Lookout, T.L.Collins 958); (g) stipitate glands on abaxial leaf surface (X. bracteatum sens. str., T.L.Collins 1005). Scale bars: 0.5 mm (a–f); 100 μm (g).
Fig. 2. Principal coordinate analysis Axes 1 and 2 in There's gold in them thar hills! Morphology and molecules delimit species in Xerochrysum (Asteraceae; Gnaphalieae) and reveal many new taxa
Fig. 2. Principal coordinate analysis Axes 1 and 2 of 2486 singlenucleotide polymorphism loci representing all species of Xerochrysum (except X. collierianum) and putative entities. Each dot represents an individual sample, coloured by population. Groups are numbered as in Table 9.
Fig. 4 in There's gold in them thar hills! Morphology and molecules delimit species in Xerochrysum (Asteraceae; Gnaphalieae) and reveal many new taxa
Fig. 4. Flagelliform trichomes and stipitate glands found on some species of Xerochrysum. Arrow with tail indicates stipitate gland; arrow without tail indicates septate trichome with flagelliform apex (cauline leaf adaxial surface, X. macsweeneyorum, T.L.Collins 957). Scale bar: 100 μm.
Fig. 1 in There's gold in them thar hills! Morphology and molecules delimit species in Xerochrysum (Asteraceae; Gnaphalieae) and reveal many new taxa
Fig. 1. Sample locations for Xerochrysum. Labelled ellipses indicate the distribution of samples included in X. bracteatum sens. lat., X. viscosum, X. macranthum, X. interiore and X. boreale. Clockwise, starting at Cape York Peninsula (the north-eastern tip of Australia): X. bracteatum sens. lat. (red circles), X. sp. North Kennedy (pale green circles), X. sp. Mount Elliot (pale green star), X. sp. North Stradbroke Island (dark blue circles), X. sp. Mount Merino (dark green circles), X. sp. Northern Tablelands (grey circles), X. sp. New England (yellow circles), X. sp. Point Lookout (pink star), X. sp. Glencoe (brown circles), X. sp. Barrington Tops (purple circles), X. aff. palustre (pink triangles), X. sp. Flinders Range (orange circles), X. subundulatum (gold triangles), X. palustre (green triangles), X. collierianum (blue triangles), X. milliganii (yellow triangle), X. alpinum (white triangle obscured by X. milliganii).
"Entanglement-induced collective many-body interference": supporting raw data
<p>Dataset for the manuscript "Entanglement-induced collective many-body interference" (<a href="https://arxiv.org/abs/2310.08630" target="_blank" rel="noopener">arXiv:2310.08630</a>).</p> <p>The dataset comprises .csv files containing measurements relevant to supporting the manuscript. Enclosed within the <strong>ECMBI.zip</strong> file are two primary folders:</p> <ol> <li> <p><strong>CoincidencesDataSet:</strong> This directory contains subdirectories with raw data supporting single and coincidence count rates.</p> <ul> <li> <p><strong>Coincidences_PsiMinus:</strong> Polarization-entangled state set to the Bell state ψ- as specified in the manuscript. The directory includes the following subdirectories:</p> <ul> <li><strong>Source1:</strong> Contains 48 CSV files of 60-second count rate measurements, sorted chronologically, when only the first photon source (Source 1) is employed. Each file contains count rate measurements for 31 different settings of the input polarization state. Within the set of 48 files, 16 files contain single-count and four-fold coincidence rates, 16 files contain three-fold coincidence rates, and 16 files contain two-fold coincidence rates. Half of the 48 files are corrected for multipair emissions (denoted by an additional Nin the file name: "*FoldN_*.csv") by rejecting events where there are coincidences in k>4 detectors (a total of 8 detectors is used).</li> <li><strong>Source2:</strong> Contains 48 CSV files of 60-second count rate measurements, sorted chronologically, when only the second photon source (Source 2) is employed. Similar to Source1, it comprises 16 files for single-count and four-fold coincidence rates, 16 files for three-fold coincidence rates, and 16 files for two-fold coincidence rates. Again, half of the 48 files are corrected for multipair emissions (denoted by an additional N in the file name: "*FoldN_*.csv").</li> <li><strong>Source1Source2:</strong> Contains 120 CSV files of 60-second count rate measurements, sorted chronologically, when both photon sources (Source 1 and Source 2) are employed. Similar to the Source1 and Source2 folders, it consists of 40 files for single-count and four-fold coincidence rates, 40 files for three-fold coincidence rates, and 40 files for two-fold coincidence rates. Once more, half of the 120 files are corrected for multipair emissions (denoted by an additional N in the file name: "*FoldN_*.csv").</li> </ul> </li> <li> <p><strong>Coincidences_PsiPlus:</strong> Polarization-entangled state set to the Bell state ψ+ as specified in the manuscript. The structure mirrors that of Coincidences_PsiMinus.</p> </li> </ul> </li> <li> <p><strong>TomographyDataSet:</strong> This folder contains raw data supporting the fidelity measurement of the polarization-entangled states ψ+ and ψ-. Two tomography stages are used to perform measurements in 36 distinct combinations of the two detectors' measuring polarization basis (e.g., H, H; H, V; H, D; H, A; H, R; H, L; V, H; etc.).</p> <ul> <li><strong>Tomography_PsiMinus:</strong> Polarization-entangled state set to the Bell state ψ-. The directory contains 6 CSV files for 6 different pumping power levels, each measuring 5-second two-fold coincidence rate for all 36 polarization bases.</li> <li><strong>Tomography_PsiPlus:</strong> Polarization-entangled state set to the Bell state ψ+. The directory content mirrors Tomography_PsiMinus.</li> </ul> </li> </ol>
Data and Codes of A Deep Learning-Based Consistency Test for Earth System Models on Heterogeneous Many-Core Systems
<p>These are the supporting information to verify the results in the paper, including input data, model outputs, the postprocessing scripts and the source codes.</p>
Data and plotting code for 'Many-body-localized discrete time crystal with a programmable spin-based quantum simulator'
<p>Underlying data and plotting for the publication: "Many-body-localized discrete time crystal with a programmable spin-based quantum simulator", J. Randall et al., 2021.</p> <p>This directory contains:</p> <p>- “Data_analysis.ipynb”: The master Jupyter notebook from which all plots produced in the main text and supplementary materials can be reproduced.<br> - “Data.zip”: A zipped folder containing the json files as loaded within “Data_analysis.ipynb”. These files contain the underlying x, y, and, where appropriate, y error values for each corresponding plot.</p> <p>The notebook should be executed using python3.</p>
Distribution. Most of Africa S of the Sahara Desert, except in lowland tropical rainforests. Spotted Hyenas have been extirpated from many areas of southern Africa. in Hyaenidae
Distribution. Most of Africa S of the Sahara Desert, except in lowland tropical rainforests. Spotted Hyenas have been extirpated from many areas of southern Africa.
Distribution. Pakistan, India, Sri Lanka, and Nepal to China, Mainland SE Asia, Peninsular Malaysia, Sumatra, Java, Borneo, the Philippines, and many ssa small islands. Also scattered records in Sulawesi, Moluccan Is, Timor, and the Aru Is, probably resulting from introductions. Presence uncertain in Papua New Guinea. Introduced to Japan in the late 1800s. in Viverridae
Distribution. Pakistan, India, Sri Lanka, and Nepal to China, Mainland SE Asia, Peninsular Malaysia, Sumatra, Java, Borneo, the Philippines, and many ssa small islands. Also scattered records in Sulawesi, Moluccan Is, Timor, and the Aru Is, probably resulting from introductions. Presence uncertain in Papua New Guinea. Introduced to Japan in the late 1800s.
Distribution. If still extant, the species would likely occur in Vietnam, and possibly in neighboring Cambodia and Laos. The true distribution of the species is unknown, because there has been very little awareness of the species. Surveys have not sought it, because many have assumed that only one species, Tragulus kanchil, occurs in most of Indochina. in Tragulidae
Distribution. If still extant, the species would likely occur in Vietnam, and possibly in neighboring Cambodia and Laos. The true distribution of the species is unknown, because there has been very little awareness of the species. Surveys have not sought it, because many have assumed that only one species, Tragulus kanchil, occurs in most of Indochina.
Data & code supplementary to the paper "Matchgate benchmarking: Scalable benchmarking of a continuous family of many-qubit gates"
<p>Code that executes and interprets the experiment displayed in fig 1 of the manuscript, as well as pickle files containing the actual data collected during the experimental run.</p>
Supplementary data for "Many-Body van der Waals Interactions in Wet MoS2 Surfaces"
<p>Supplementary data for "Many-Body van der Waals Interactions in Wet MoS2 Surfaces"</p>
Distribution. Most of Africa S of the Sahara Desert, except in lowland tropical rainforests. Spotted Hyenas have been extirpated from many areas of southern Africa. in Hyaenidae
Distribution. Most of Africa S of the Sahara Desert, except in lowland tropical rainforests. Spotted Hyenas have been extirpated from many areas of southern Africa.
Distribution. Coastal NW Mexico, including areas in Sebastian Vizcaino Bay and Tortuga Bay on Pacific coast, Gulf of California from C Baja California (Islas Esmeraldas) to Bay of Paz and Punta Coyotes in Baja California Sur, and from Bay of San Jorge S to Guaymas in Sonora; also on many islands. in Vespertilionidae
Distribution. Coastal NW Mexico, including areas in Sebastian Vizcaino Bay and Tortuga Bay on Pacific coast, Gulf of California from C Baja California (Islas Esmeraldas) to Bay of Paz and Punta Coyotes in Baja California Sur, and from Bay of San Jorge S to Guaymas in Sonora; also on many islands.
Distribution. SW Russian Far East (Ussuri region), North and South Korea, Japan including many offshore Is (Tsushima, Yakushima, Tanegashima, Kuchinoshima, Takarajima, Amami-Oshima, Kakeroma-Jima, Tokunoshima, Okinawajima, Miyakojima, Irabu, Ishigakijima, Iriomotejima, and Yonagunijima), C, E & S China, Taiwan and Hainan Is, N Myanmar, N Laos, N & C Vietnam (including Cat Ba and Kaitien Is), and scattered records in NC, SC & NE India (Uttar Pradesh, Arunachal Pradesh, and Andhra Pradesh); there is a record from Sakhalin I, but this requires confirmation. in Vespertilionidae
Distribution. SW Russian Far East (Ussuri region), North and South Korea, Japan including many offshore Is (Tsushima, Yakushima, Tanegashima, Kuchinoshima, Takarajima, Amami-Oshima, Kakeroma-Jima, Tokunoshima, Okinawajima, Miyakojima, Irabu, Ishigakijima, Iriomotejima, and Yonagunijima), C, E & S China, Taiwan and Hainan Is, N Myanmar, N Laos, N & C Vietnam (including Cat Ba and Kaitien Is), and scattered records in NC, SC & NE India (Uttar Pradesh, Arunachal Pradesh, and Andhra Pradesh); there is a record from Sakhalin I, but this requires confirmation.
Distribution. NE India, NE Bangladesh, S China (including Hainan I), mainland SE Asia, Sumatra (including Simeulue, Nias, and Mentawai Is), Borneo, Java, Kangean, Bali, and many offshore Is. in Hipposideridae
Distribution. NE India, NE Bangladesh, S China (including Hainan I), mainland SE Asia, Sumatra (including Simeulue, Nias, and Mentawai Is), Borneo, Java, Kangean, Bali, and many offshore Is.
Data and Codes of Characterizing Uncertainties of Earth System Modeling with Heterogeneous Many-core Architecture Computing
<p>These are the supporting information to verify the results in the paper, including input data, model outputs, the postprocessing scripts and the source codes.</p>
Many ways to make darker flies: Intra- and inter-specific variation in Drosophila body pigmentation components
Body pigmentation is an evolutionarily diversified and ecologically relevant trait with substantial variation within and between species, and important roles in animal survival and reproduction. Insect pigmentation, in particular, provides some of the most compelling examples of adaptive evolution, including its ecological significance and genetic bases. Pigmentation includes multiple aspects of color and color pattern that may vary more or less independently, and can be under different selective pressures. We decompose Drosophila thorax and abdominal pigmentation, a valuable eco-evo-devo model, into distinct measurable traits related to color and color pattern. We investigate intra- and inter-specific variation for those traits, and assess its different sources. For each body part, we measured overall darkness, as well as four other pigmentation properties distinguishing between background color and color of the darker pattern elements that decorate each body part. By focusing on two standard D. melanogaster laboratory populations, we show that pigmentation components vary and co-vary in distinct manners depending on sex, genetic background, and temperature during development. Studying three natural populations of D. melanogaster along a latitudinal cline and five other Drosophila species, we then show that evolution of lighter or darker bodies can be achieved by changing distinct component traits. Our results paint a much more complex picture of body pigmentation variation than previous studies could uncover, including patterns of sexual dimorphism, thermal plasticity, and inter-specific diversity. These findings underscore the value of detailed quantitative phenotyping and analysis of different sources of variation for a better understanding of phenotypic variation and diversification, and the ecological pressures and genetic mechanisms underlying them.
Subspecies and Distribution. R.t.timorensisdeBlainville,1822—TimorI. R.t.djongaVanBemmel,1949-MunaandButonIs. R.t.flovesiensisHeude,1897—Flores1. R.t.macassaricaHeude,1896—Sulawesi. R.t.moluccensisQuoy&Gaimard,1830—MoluccanIs. R.t.renschiSody,1932—Bali. R. t. russa Muller & Schlegel, 1845 — Java. Possibly it is native only to Java and Bali islands, introduced into Lombok, Flores, Sumbawa, Sumba, Timor, Sulawesi, and Moluccan Islands in ancient times. It was introduced during the last centuries in many locations, including New Guinea, Aru Islands, New Britain Is, Australia, New Zealand, New Caledonia, Mauritius, and Comoro Is. The map represents the native range and the oldest introductions. in Cervidae
Subspecies and Distribution. R.t.timorensisdeBlainville,1822—TimorI. R.t.djongaVanBemmel,1949-MunaandButonIs. R.t.flovesiensisHeude,1897—Flores1. R.t.macassaricaHeude,1896—Sulawesi. R.t.moluccensisQuoy&Gaimard,1830—MoluccanIs. R.t.renschiSody,1932—Bali. R. t. russa Muller & Schlegel, 1845 — Java. Possibly it is native only to Java and Bali islands, introduced into Lombok, Flores, Sumbawa, Sumba, Timor, Sulawesi, and Moluccan Islands in ancient times. It was introduced during the last centuries in many locations, including New Guinea, Aru Islands, New Britain Is, Australia, New Zealand, New Caledonia, Mauritius, and Comoro Is. The map represents the native range and the oldest introductions.
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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.