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Bulk Domain Names (30-Jan-2015 - Last Update) -- varocarbas.com
<p>This post refers to an old set of outdated information. </p> <p>The system extracting those links was the precursor of the current web domain ranking in https://varocarbas.com/domain_ranking/</p> <p> </p> <p>CLARIFICATION: this has nothing to do with marketing, SEO or paid anything. The sole purpose of this system now and ever has been to show my software development skills and related issues (e.g., big system running on very restricted hardware). All the displayed information is meant to show the actual reality as objectively as possible. </p> <p>There is only one way to be part of the aforementioned ranking or to get a better/worse position in it: the system (crawling bots, ranking algorithms, correction subsystems, etc.) voluntarily deciding so.</p>
Annotated genes harboring major effect markers (R2 ≥ 15%). Highlighted in green are genes annotated from Rhodes et al. 2014,2017, in orange genes annotated as similar to Peroxidase, in yellow new annotations from sorghum genome in Atlas. In the first three columns start and stop position on the sorghum genome and transcript name, followed by the nearest marker name and the distance of the gene from the nearest marker, then a column where are shown the GWAS methods and target traits for which the linked SNP was significant, the last column shows the category of the genes.
<p><strong>We conducted a comprehensive genomics study to map genomic loci determining the production of antioxidants in sorghum grains. Encouraging results were obtained and published in peer-reviewed article with impact factor (https://doi.org/10.1371/journal.pone.0225979). Annotated genes harboring major effect markers (R<sup>2</sup> ≥ 15%) were identified and will be of worldwide interest. </strong></p>
FIGURE 10 in Kalanchoe ×trageri, at last a name for K. blossfeldiana × K. pumila (Crassulaceae subfam. Kalanchooideae), a horticulturally successful nothospecies
FIGURE 10. John Noyes (John) Trager (1957–) after whom Kalanchoe ×trageri is named. Photograph: Daphne Trager.
FIGURE 9 in Kalanchoe ×trageri, at last a name for K. blossfeldiana × K. pumila (Crassulaceae subfam. Kalanchooideae), a horticulturally successful nothospecies
FIGURE 9. Comparison of the shape and size of the corolla segments viewed from the mouth, i.e., from above, of Kalanchoe blossfeldiana (left), K. ×trageri (centre), and K. pumila (right). Scale bar = 5 mm. Photograph: Gideon F. Smith.
FIGURE 8 in Kalanchoe ×trageri, at last a name for K. blossfeldiana × K. pumila (Crassulaceae subfam. Kalanchooideae), a horticulturally successful nothospecies
FIGURE 8. Comparison of the flowers of Kalanchoe blossfeldiana (left), K. ×trageri (centre), and K. pumila (right), in lateral view. Scale bar = 5 mm. Photograph: Gideon F. Smith.
FIGURE 6 in Kalanchoe ×trageri, at last a name for K. blossfeldiana × K. pumila (Crassulaceae subfam. Kalanchooideae), a horticulturally successful nothospecies
FIGURE 6. The aberrant flower of Kalanchoe ×trageri on the left is pentamerous, rather than tetramerous as in the case of the vast majority of Kalanchoe species. Note that the leaf crenations terminate in a sharper tip than in the case of K. blossfeldiana. Photograph: Gideon F. Smith.
FIGURE 5 in Kalanchoe ×trageri, at last a name for K. blossfeldiana × K. pumila (Crassulaceae subfam. Kalanchooideae), a horticulturally successful nothospecies
FIGURE 5. The adaxial surfaces of the corolla lobes of Kalanchoe ×trageri are bright, dark reddish purple. The corolla lobes are ultimately strongly recurved, as in K. pumila. Photograph: Gideon F. Smith.
FIGURE 7 in Kalanchoe ×trageri, at last a name for K. blossfeldiana × K. pumila (Crassulaceae subfam. Kalanchooideae), a horticulturally successful nothospecies
FIGURE 7. Comparison of leaves of Kalanchoe blossfeldiana (left), K. ×trageri (centre), and K. pumila (right). Note that leaves of K. blossfeldiana are variable in size. The white, floury wax was deliberately removed from the leaf surface of K. pumila. Scale bar = 10 mm. Photograph: Gideon F. Smith.
FIGURE 2 in Kalanchoe ×trageri, at last a name for K. blossfeldiana × K. pumila (Crassulaceae subfam. Kalanchooideae), a horticulturally successful nothospecies
FIGURE 2. The corolla lobes of Kalanchoe pumila are usually strongly recurved and various shades of pink with longitudinal purple lines. Photograph: Gideon F. Smith.
FIGURE 1 in Kalanchoe ×trageri, at last a name for K. blossfeldiana × K. pumila (Crassulaceae subfam. Kalanchooideae), a horticulturally successful nothospecies
FIGURE 1. The adaxial surfaces of the corolla lobes of Kalanchoe blossfeldiana are bright crimson red. The lobes are spreading rather than recurved. Photograph: Gideon F. Smith.
Deccan region, Madras, India. Genus Vandeleuria is masculine, so widely used specific name oleracea has been changed for gender agreement. Vandeleuria oleraceusis possibly a composite of species. Polytypic, but subspecific taxonomy requires reassessment. Distribution. Widespread in S Asia (India, Nepal, Bhutan, Bangladesh, and Sri Lan-ka), S China (W & S Yunnan), and mainland SE Asia N of the Isthmus of Kra. Descriptive notes. Head-body 68 mm, tail 105 mm, ear 13 mm, hindfoot 17 mm; weight 10 g. The Indomalayan Long-tailed Climbing Mouse is small, with flat nail on outer finger and outertoe; tail is slender, brown, twice as long as head-body length, and lacks distal tuft. Dorsal pelageis silky and salmon in color; venter is white, with fulvous hues. Habitat. Tall cane and tangled vines in primary and secondary forest such as bamboo forest, moist deciduous forest, temperate forests, montane wet zone, and disturbed secondary forests, and perhaps agricultural areas at elevations of 150-1500 m. Food and Feeding. Indomalayan [Long-tailed Climbing Mice eat fruits, buds, and flowers. Breeding. Litters of the Indomalayan Long-tailed Climbing Mouse have 3-6 young. Activity patterns. Indomalayan Long-tailed Climbing Mice are arboreal and nocturnal, although one individual was caught duringthe day. Movements, Home range and Social organization. Indomalayan Long-tailed Climbing Mice build nests in tall bushes or cane to rear their young. Status and Conservation. Classified as Least Concern on The IUCN Red Last (as V. olacea). The Indomalayan Long-tailed Climbing Mouse occurs in several habitats and a wide distribution that includes national parks. Further taxonomical studies are required to assess conservation status ofthis potentially diverse species complex. Bibliography. Corbet & Hill (1992), Dang Huy Huynh et al. (1994), Ellerman (1941), Marshall (1977b), Musser & Carleton (2005), Osgood (1932), Phillips (1980), Wang Yingxiang (2003). in Muridae
Deccan region, Madras, India. Genus Vandeleuria is masculine, so widely used specific name oleracea has been changed for gender agreement. Vandeleuria oleraceusis possibly a composite of species. Polytypic, but subspecific taxonomy requires reassessment. Distribution. Widespread in S Asia (India, Nepal, Bhutan, Bangladesh, and Sri Lan-ka), S China (W & S Yunnan), and mainland SE Asia N of the Isthmus of Kra. Descriptive notes. Head-body 68 mm, tail 105 mm, ear 13 mm, hindfoot 17 mm; weight 10 g. The Indomalayan Long-tailed Climbing Mouse is small, with flat nail on outer finger and outertoe; tail is slender, brown, twice as long as head-body length, and lacks distal tuft. Dorsal pelageis silky and salmon in color; venter is white, with fulvous hues. Habitat. Tall cane and tangled vines in primary and secondary forest such as bamboo forest, moist deciduous forest, temperate forests, montane wet zone, and disturbed secondary forests, and perhaps agricultural areas at elevations of 150-1500 m. Food and Feeding. Indomalayan [Long-tailed Climbing Mice eat fruits, buds, and flowers. Breeding. Litters of the Indomalayan Long-tailed Climbing Mouse have 3-6 young. Activity patterns. Indomalayan Long-tailed Climbing Mice are arboreal and nocturnal, although one individual was caught duringthe day. Movements, Home range and Social organization. Indomalayan Long-tailed Climbing Mice build nests in tall bushes or cane to rear their young. Status and Conservation. Classified as Least Concern on The IUCN Red Last (as V. olacea). The Indomalayan Long-tailed Climbing Mouse occurs in several habitats and a wide distribution that includes national parks. Further taxonomical studies are required to assess conservation status ofthis potentially diverse species complex. Bibliography. Corbet & Hill (1992), Dang Huy Huynh et al. (1994), Ellerman (1941), Marshall (1977b), Musser & Carleton (2005), Osgood (1932), Phillips (1980), Wang Yingxiang (2003).
FIGURES 11‒17. Last instar larva. 11 in Anarsioses, a new generic name for Phyllonorycter aberrans (Braun) (Lepidoptera Gracillariidae)
FIGURES 11‒17. Last instar larva. 11. Lateral schematic of prothorax, mesothorax, and abdominal segments 1, 2, 5‒10. 12. Head, dorsal view. 13. Head, ventral view. 14. Head, lateral view. 15. Dorsal view of abdominal segments 8–10. 16. Labrum, dorsal view. 17. Mandible, ventral view.
FIG UR E 3 (a) Dated phylogeny of the genus Theodoxus constructed in BEAST based on COI, 16S and ATPα. Node labels denote divergence times in millions of years ago (Ma); node bars indicate the 95% credibility interval around these dates. Small squares at nodes indicate significant support of divergence events found with BEAST and other phylogenetic analyses (see Figures S2.1 and S2.2), as explained through the key. Where MOTUs (A–R) show conspecifics among a number of morphospecies, species names are given in order of their year of description. Morphospecies, incorporated from GenBank, where determination was potentially dubious are highlighted by an asterisk. Clades (C) and subclades (SC) are demarcated by dashed lines between MOTUs. (b) LTT plots indicating the build‐up of lineages in Theodoxus over geological time. Dashed lines surrounding the solid LTT lines indicate the 95% confidence intervals. Where intra‐ and interspecific diversity diverge, interspecific diversity is highlighted in blue and intraspecific diversity in red. Transitions in geological ages are highlighted by narrow grey lines, while the grey bar marks the period of pronounced glacial cycles (last 900 kyr) [Colour figure can be viewed at wileyonlinelibrary.com] in Contributions of biogeographical functions to species accumulation may change over time in refugial regions
FIG UR E 3 (a) Dated phylogeny of the genus Theodoxus constructed in BEAST based on COI, 16S and ATPα. Node labels denote divergence times in millions of years ago (Ma); node bars indicate the 95% credibility interval around these dates. Small squares at nodes indicate significant support of divergence events found with BEAST and other phylogenetic analyses (see Figures S2.1 and S2.2), as explained through the key. Where MOTUs (A–R) show conspecifics among a number of morphospecies, species names are given in order of their year of description. Morphospecies, incorporated from GenBank, where determination was potentially dubious are highlighted by an asterisk. Clades (C) and subclades (SC) are demarcated by dashed lines between MOTUs. (b) LTT plots indicating the build‐up of lineages in Theodoxus over geological time. Dashed lines surrounding the solid LTT lines indicate the 95% confidence intervals. Where intra‐ and interspecific diversity diverge, interspecific diversity is highlighted in blue and intraspecific diversity in red. Transitions in geological ages are highlighted by narrow grey lines, while the grey bar marks the period of pronounced glacial cycles (last 900 kyr) [Colour figure can be viewed at wileyonlinelibrary.com]
FIGURE 4 in Kalanchoe ×trageri, at last a name for K. blossfeldiana × K. pumila (Crassulaceae subfam. Kalanchooideae), a horticulturally successful nothospecies
FIGURE 4. Dense-flowered inflorescences of Kalanchoe ×trageri. Photograph: Gideon F. Smith.
FIGURE 3. A in Kalanchoe ×trageri, at last a name for K. blossfeldiana × K. pumila (Crassulaceae subfam. Kalanchooideae), a horticulturally successful nothospecies
FIGURE 3. A plant of Kalanchoe ×trageri. Note how the leaves are variously flexed from the horizontal, as is often found in K. pumila, one of its parents. Photograph: Gideon F. Smith.
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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.