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22,455 results for “Diversion”
Table 1 in Latitudinal Diversity Gradients in Free-living Microorganisms - Hoogenraadia a Key Genus in Testate Amoebae Biogeography
<p><b>Table 1.</b> Characters and distribution of six species of the genus <i>Hoogenraadia</i> (L – length, W – width). Many of the earlier papers do not report a sample size for number of tests measured – so it is possible that some of these data may be based on a very low sample size.</p><table><tbody><tr><th>Species</th><th>Size <b>(</b>µm<b>)</b></th><th>Distribution regions and publication</th><th>Habitats</th></tr></tbody><tbody><tr><th><i>H. africana</i></th><td>L = 95–115, W = 47–60</td><td>Moyen-Congo (Gauthier-Lièvre and Thomas 1958), Guinea and Equatorial Guinea (Golemansky 1962), Brasil (Leiptniz <i>et al</i>. 2003), China (Qin <i>et al</i>. 2011)</td><td><i>Sphagnum</i>, water, river, forest marsh</td></tr><tr><th><i>H. asiatica</i></th><td>L = 95, W = 70</td><td>China (Wang and Min 1987)</td><td>Quaternary deposit</td></tr><tr><th><i>H. cryptostoma</i></th><td>L = 130–140, W = 105–110</td><td>Moyen-Congo (Gauthier-Lièvre and Thomas 1958), States of Parana, Mato Grosso du Sul, Brasil (Velho <i>et al</i>. 1996, 2000)</td><td>Swamp quite shady in the bed of a stream</td></tr><tr><th><i>H. humicola</i></th><td>L = 143–146, W = 96–100</td><td>Nepal, Himalayas (Bonnet 1977, 1978), Philippines (Bonnet 1980), Cote d’Ivoire, Africa (Bonnet 1976, 1978), Tonga and Western Samoa Islands (Korganova 1994), China (this paper)</td><td>Soils rich in organic debris in forest-gallery backwaters. The ground litter and sublitter horizons of white subtropical soils</td></tr><tr><th><i>H. ovata</i></th><td>L = 60–67, W = 36–39</td><td>Cote d’Ivoire, Africa (Bonnet 1976)</td><td>Soils rich in organic debris in forest-gallery backwaters</td></tr><tr><th><i>H. sylvatica</i></th><td>L = 82–93, W = 60–70</td><td>Punta Lara Province of Buenos Aires, Argentina (Vucetich 1974)</td><td>Moss in marginal forest</td></tr></tbody></table>
Supplemental data for: Structural polymorphism and diversity of human segmental duplications
<p>Data used for figure generation and analysis in: Structural polymorphism and diversity of human segmental duplications</p> <p> </p> <p>Code used for data analysis is on https://github.com/hrrsjeong/pangenome_SD</p>
UV radiation accelerates litter decomposition in a valley-type savanna by enhancing microbial community diversity and function
<p><span>We present the data of the study by Gao et al. (202</span><span>4</span><span>): <a name="_Hlk179470571"></a><a name="OLE_LINK42"></a><strong><span>UV radiation accelerates litter decomposition in a valley-type savanna by enhancing microbial community diversity and function</span></strong></span><span>.</span><span> The excel file (Raw Data) includes the following sheets: 1- Radiation (w·m<sup>-2</sup>) variation of UV-A and UV-B during the experimental period. 2- Decay constants (<em>K</em>, yr<sup>−1</sup>) and changes in the mass loss rate of litter under different UV conditions during the experimental period<span>. 3- </span>The content of lignin, cellulose, C, N and P of litter under different UV conditions during the experimental period<span>. 4-</span></span><span> </span><span>16S ASVs under different UV conditions<span>. 5-</span></span><span> </span><span>ITS ASVs under different UV conditions.</span></p>
Fig 10 in Correction: Integrated Taxonomy Reveals Hidden Diversity in Northern Australian Fishes: A New Species of Seamoth (Genus Pegasus)
Fig 10. Molecular species identification of Pegasus species using Genetic treeML trees. (A) sequences from the 16S gene; (B) sequences from the COI gene. Trees are based on the K2 evolutionary distance model and are shown here with mined Pegasus and Eurypegasus sequences from GenBank. The trees are shown here with an E. draconis outgroup. Bootstrap support values (following 1000 replicates) are shown above the nodes. https://doi.org/10.1371/journal.pone.0251680.g001
Data underlying the assessment of biodiversity and diverse values for nature in University of Helsinki campuses / Aineisto luonnon monimuotoisuutta ja moninaisia arvoja Helsingin yliopiston kampuksilla käsittelevän selvitystyön taustalla
<p>These records contain the spatial and nonspatial datasets underlying the assessment of biodiversity and diverse values for nature in the four campuses of University of Helsinki, namely the Kumpula, Meilahti, Viikki, and City center campuses in Helsinki. The assessment was a part of the University of Helsinki Sustainability and responsibility plan 2022-2024.</p> <p>For further information on the types and contents of the data, see the pdf "README.pdf" and the assessment report.</p> <p> </p>
Interactive and unimodal relationships between plant biomass, abiotic factors, and plant diversity in global grasslands
<p>The R file CodeGrasslandBiomass contains all R code necessary to reproduce all results of the manuscript “Interactive and unimodal relationships between plant biomass, abiotic factors, and plant diversity in global grasslands” based on the data in the csv file DataGB.</p> <p> </p>
Tilapia genetic diversity across the Lake Victoria Basin
<p>Genotypes for <em>Oreochromis niloticus</em>, <em>O. leucosticus,</em> <em>O. variabilis</em>, <em>O. esculentus</em>, <em>Coptodon rendalli</em>, <em>C. zillii </em>collected in water bodies in Kenya, Tanzania, and Uganda within the Lake Victoria Basin. </p> <p> </p>
Diverse Dataset for Eyeglasses Detection: Extending the Flickr-Faces-HQ (FFHQ) Dataset
<p>Extension of the FFHQ dataset (https://github.com/NVlabs/ffhq-dataset) with precise bounding box annotations for eyeglasses detection.</p> <p>If you find this dataset useful in your research, please consider citing the original dataset and the following papers:</p> <p>@article{matuzevicius2024diverse,<br> title={Diverse Dataset for Eyeglasses Detection: Extending the Flickr-Faces-HQ (FFHQ) Dataset},<br> author={Matuzevi{\v{c}}ius, Dalius},<br> journal={Sensors},<br> volume={24},<br> number={23},<br> pages={7697},<br> year={2024},<br> publisher={MDPI},<br> url = {https://doi.org/10.3390/s24237697}<br>}</p> <p>@article{matuzevicius2024retrospective,<br> title={A Retrospective Analysis of Automated Image Labeling for Eyewear Detection Using Zero-Shot Object Detectors},<br> author={Matuzevi{\v{c}}ius, Dalius},<br> journal={Electronics},<br> volume={13},<br> number={23},<br> pages={4763},<br> year={2024},<br> publisher={MDPI},<br> url = {https://doi.org/10.3390/electronics13234763}<br>}</p> <p> </p>
Diversity of radial variations of wood properties in European beech reveals the plastic nature of juvenile wood - Dataset
<p>The long-term (as opposed to short-term intra-ring) radial variation of wood properties in European beech (<em>Fagus sylvatica</em> L.) from pith to bark are largest in the young ages of the tree (internal core). This so-called juvenility reflects both cambium ageing (ontogenetic juvenility) and adaptation to the changing mechanical constraints during secondary growth (adaptive juvenility). Ring width (<em>RW</em>), specific gravity (<em>SG</em>) and specific modulus (<em>SM</em>) are important parameters for each new wood layer, needed for the study of mechanical stability of a standing tree. They should be sensitive to the mechanical adaptation of growth.<strong> </strong>They were measured on diametrical boards (North/South direction) issued from 86 trees from several high forest stands in European countries. Analysis of variance showed very significant influence of position within the tree (core/external), of trees within a plot and of plots, but not for North/South orientation. The share of variance was similar for <em>SG</em> and <em>SM</em> (importance of tree effect) but different for <em>RW </em>(importance of plot effect). The occurrence of red heartwood in the core on some trees had a significant influence, mostly on <em>SM</em>, but the differences between white and red wood was very small. Globally the variability was high for <em>RW</em>, rather small for <em>SM</em> and very small for <em>SG</em>. Accordingly, the variations of the modulus of elasticity (product of <em>SG</em> and <em>SM</em>) were much more influenced by <em>SM</em> than by <em>SG</em> for beech. The radial variations of each parameter were fitted by both a linear (2 coefficients: zero value and mean slope) and a parabolic curve (3 coefficients: zero value, initial slope and curvature). They were used to classify types or radial profile in terms of flat, up & down and straight, convex & concave. Median values of coefficients per plot (or total) were used to draw median profiles for each parameter per plot and at the global level. The median global profiles differed from the typical radial pattern (TRP) of juvenility for plantation softwoods for <em>SG</em> (down concave instead of up concave) and <em>SM</em> (convex like TRP but with a clear decrease in the mature wood). The main result was the very large variability of profiles between trees or even between plots. Even if there is a part of ontogenetic influence in the juvenile patterns for <em>RW</em>, <em>SG</em> and <em>SM</em>, the results suggest that the influence of mechanical constraints on tree growth (adaptive juvenility) dominates largely. </p> <p><em>The provided file contains the data and the sheets developped to analyse them. It serves as supplementary material for the related paper submitted for recommendation to the PCI Forest and Wood Science.</em></p>
Fig. 11. Nemastoma bidentatum Roewer, 1914 in Hidden diversity within the Nemastoma bidentatum Roewer, 1914 complex (Opiliones: Nemastomatidae) Part I: Morphological evidence
Fig. 11. Nemastoma bidentatum Roewer, 1914 complex, ♀♀; Rec sem (lateral view, right portion, except F left figure, which is in dorsal view). A. The frame encloses the ovipositor portion with Rec sem. Note: Female N. pluridentatum (Hadži, 1973) stat. nov. is unknown.
Fig. 10. Nemastoma bidentatum Roewer, 1914 in Hidden diversity within the Nemastoma bidentatum Roewer, 1914 complex (Opiliones: Nemastomatidae) Part I: Morphological evidence
Fig. 10. Nemastoma bidentatum Roewer, 1914 complex, ♂♂. Variation of the Pa-Fe (A–B first image, C, D–E first image, F–G first image; H–J, L–M right, N–O: lateral view; the others in dorso-medial view to show the armament).
Fig. 6. Nemastoma bidentatum Roewer, 1914 in Hidden diversity within the Nemastoma bidentatum Roewer, 1914 complex (Opiliones: Nemastomatidae) Part I: Morphological evidence
Fig. 6. Nemastoma bidentatum Roewer, 1914 complex, ♂♂. Synchroscopic images of the male Ch basal article and Pa-Fe (medial views, except G, right figure, which is in dorso-medial view).
Fig. 9. Nemastoma bidentatum Roewer, 1914 in Hidden diversity within the Nemastoma bidentatum Roewer, 1914 complex (Opiliones: Nemastomatidae) Part I: Morphological evidence
Fig. 9. Nemastoma bidentatum Roewer, 1914 complex, ♂♂. Variation of the Ch basal article (medial view) in species, subspecies and hybrids.
Fig. 2 in Hidden diversity within the Nemastoma bidentatum Roewer, 1914 complex (Opiliones: Nemastomatidae) Part I: Morphological evidence
Fig. 2. The complete distributional area of the Nemastoma bidentatum Roewer, 1914 complex, according to Gruber & Martens (1968), Martens (2006), Schönhofer & Holle (2007) and own data, with marked positions of the type localities of the taxa.
Fig. 13. Nemastoma bidentatum Roewer, 1914 in Hidden diversity within the Nemastoma bidentatum Roewer, 1914 complex (Opiliones: Nemastomatidae) Part I: Morphological evidence
Fig. 13. Nemastoma bidentatum Roewer, 1914 complex, ♀♀. From left to right: Silhouettes of the Ch basal article, Pa (both medial view) and Rec sem. Arrows indicate the most identifying characters. Note: female N. pluridentatum (Hadži, 1973) stat. nov. is unknown.
Fig. 12. Nemastoma bidentatum Roewer, 1914 in Hidden diversity within the Nemastoma bidentatum Roewer, 1914 complex (Opiliones: Nemastomatidae) Part I: Morphological evidence
Fig. 12. Nemastoma bidentatum Roewer, 1914 complex, ♂♂. From left to right: Ch basal article (medial, lateral views), Pa (medial view) and Pe tip (dorsal, lateral views). Arrows indicate the most identifying characters. Note: Pe of N. pluridentatum (Hadži, 1973) stat. nov. is unknown.
Fig. 8. Nemastoma bidentatum Roewer, 1914 in Hidden diversity within the Nemastoma bidentatum Roewer, 1914 complex (Opiliones: Nemastomatidae) Part I: Morphological evidence
Fig. 8. Nemastoma bidentatum Roewer, 1914 complex. Glans (dorsal and lateral views). Note: The penis of N. pluridentatum (Hadži, 1973) stat. nov. is unknown.
Fig. 7. Nemastoma bidentatum Roewer, 1914 in Hidden diversity within the Nemastoma bidentatum Roewer, 1914 complex (Opiliones: Nemastomatidae) Part I: Morphological evidence
Fig. 7. Nemastoma bidentatum Roewer, 1914 complex. Penes (lateral view). Note: The penis of N. pluridentatum (Hadži, 1973) stat. nov. is unknown.
FIG. 13 in Field inventory reveals high diversity of new species of mountain catfishes, genus Cambeva Katz, Barbosa, Mattos & Costa, 2018 (Siluriformes: Trichomycteridae), in south-eastern Serra Geral, southern Brazil
FIG. 13. — Urohyal, ventral view. A, Cambeva diffusa n. sp.; B, Cambeva pericoh n. sp.; C, Cambeva imaruhy n. sp.; D, Cambeva orbitofrontalis n. sp.; E, Cambeva panthera n. sp.; F, Cambeva grisea n. sp.; G, Cambeva duplimaculata n. sp.; H, Cambeva longipalata n. sp.; I, Cambeva notabilis n. sp.; J, Cambeva urubici n. sp.
FIG. 12 in Field inventory reveals high diversity of new species of mountain catfishes, genus Cambeva Katz, Barbosa, Mattos & Costa, 2018 (Siluriformes: Trichomycteridae), in south-eastern Serra Geral, southern Brazil
FIG. 12. — Left suspensorium and opercular series, lateral view: A, Cambeva diffusa n. sp.; B, Cambeva pericoh n. sp.; C, Cambeva imaruhy n. sp.; D, Cambeva orbitofrontalis n. sp.; E, Cambeva panthera n. sp.; F, Cambeva grisea n. sp.; G, Cambeva duplimaculata n. sp.; H, Cambeva longipalata n. sp.; I, Cambeva notabilis n. sp.; J, Cambeva urubici n. sp. Abbreviations of structures indicated by arrows are: iac, interopercular anterior concavity; ppe, preopercular postero-dorsal expansion; odc, opercular dorsal constriction; odp, opercular dorsal process; ppp, parurohyal posterior process. Larger stippling represents cartilaginous areas.
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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)
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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.