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1,427 results for “vine”
Gelsemium sempervirens (Loganiaceae) - whole tree (or vine) - general
Image of Gelsemium sempervirens (Loganiaceae) - whole tree (or vine) - general
Callicarpa americana (Verbenaceae) - whole tree (or vine) - general
Image of Callicarpa americana (Verbenaceae) - whole tree (or vine) - general
Cephalanthus occidentalis (Rubiaceae) - whole tree (or vine) - general
Image of Cephalanthus occidentalis (Rubiaceae) - whole tree (or vine) - general
Hibiscus moscheutos ssp. lasiocarpos (Malvaceae) - whole tree (or vine) - general
Image of Hibiscus moscheutos ssp. lasiocarpos (Malvaceae) - whole tree (or vine) - general
Hypericum hypericoides (Clusiaceae) - whole tree (or vine) - general
Image of Hypericum hypericoides (Clusiaceae) - whole tree (or vine) - general
Campsis radicans (Bignoniaceae) - whole tree (or vine) - general
Image of Campsis radicans (Bignoniaceae) - whole tree (or vine) - general
Figure 4 in Adding missing vines to the tree: multilocus phylogeny of New World vine snakes (Serpentes: Colubridae: Oxybelis), with description of a new species
Figure 4. Heads of Oxybelis transandinus sp. nov. in lateral view. Paratypes QCAZ 15804 (A), 16039 (B), 17096 (C), and 14448 (D). Photographs by G. Pazmiño-Otamendi (A), D. Núñez (B, C), F. Ayala-Varela (D).
Figure 3 in Adding missing vines to the tree: multilocus phylogeny of New World vine snakes (Serpentes: Colubridae: Oxybelis), with description of a new species
Figure 3. Male holotype (QCAZ 17097, total length = 106.3 cm) of Oxybelis transandinus sp. nov. in dorsal (A) and ventral (B) views. Photographs by M. Mejía-Guerrero. Scale bars = 10 mm.
Figure 1 in Adding missing vines to the tree: multilocus phylogeny of New World vine snakes (Serpentes: Colubridae: Oxybelis), with description of a new species
Figure 1. Phylogeny of Oxybelis. Maximum clade credibility tree obtained from a phylogenetic analysis of four mitochondrial (12S, 16S, CYTB, ND4) and two nuclear genes (CMOS, PRLR). Posterior probabilities and RAxML rapid-bootstrap support values are shown above and below branches, respectively; for clarity, support values on short branches are not shown. Voucher number and country is indicated for each terminal. Specimens of the new species described in this paper are coloured in red. Outgroup taxa are not shown. GenBank accession numbers along with more detailed locality data are presented in Table 1.
Figure 6 in Adding missing vines to the tree: multilocus phylogeny of New World vine snakes (Serpentes: Colubridae: Oxybelis), with description of a new species
Figure 6. Specimen of Oxybelis inkaterra from Ecuador (QCAZ 5207) in dorsal (A) and ventral (B) views. Close-up of head in dorsal (C) and ventral (D) views. Photographs by J. Carrión. Scales bars = 10 mm.
Figure 5 in Adding missing vines to the tree: multilocus phylogeny of New World vine snakes (Serpentes: Colubridae: Oxybelis), with description of a new species
Figure 5. Known distribution of Oxybelis transandinus sp. nov. (circles) and O. inkaterra (triangle) in Ecuador. Star represents type locality of O. transandinus. Specimens sequenced in this study are shown in red.
Figure 2 in Adding missing vines to the tree: multilocus phylogeny of New World vine snakes (Serpentes: Colubridae: Oxybelis), with description of a new species
Figure 2. Male holotype (QCAZ 17097, total length = 106.3 cm) of Oxybelis transandinus sp. nov. in life. General views of body (A, B), and dorsal, ventral and lateral views of head (C). Photographs by M. Rivera. Scale bar (C) = 10 mm.
The genetic architectures of vine and skin maturity in tetraploid potato
<p>Potato vine and skin maturity, which refer to foliar senescence and adherence of the tuber periderm, respectively, are both important to production and therefore breeding. Our objective was to investigate the genetic architectures of these traits in a genome-wide association panel of 586 genotypes, and through joint linkage mapping in a half-diallel subset (N = 397). Skin maturity was measured by image analysis after mechanized harvest 120 days after planting. To correct for the influence of vine maturity on skin maturity under these conditions, the former was used as a covariate in the analysis. The genomic heritability based on a 10K SNP array was 0.33 for skin maturity vs. 0.46 for vine maturity. Only minor QTL were detected for skin maturity, the largest being on chromosome 9 and explaining 8% of the variation. As in many previous studies, <em>S. tuberosum Cycling DOF Factor 1</em> (<em>CDF1</em>) had a large influence on vine maturity, explaining 33% of the variation in the panel as a bi-allelic SNP and 44% in the half-diallel as a multi-allelic QTL. From the estimated effects of the parental haplotypes in the half-diallel and prior knowledge of the allelic series for <em>CDF1</em>, the <em>CDF1 </em>allele for each haplotype was predicted and ultimately confirmed through whole-genome sequencing. The ability to connect statistical alleles from QTL models with biological alleles based on DNA sequencing represents a new milestone in genomics-assisted breeding for tetraploid species.</p>
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).
Predicting the global potential distribution of vine mealybug, Planococcus ficus under climate change
<p>Figure S1: Performances of niche model of <em>P.ficus</em> in current model. L=Linear; Q=Quadratic; H=Hinge; P=Product; T=Threshold, Figure S2: Partial AUC Values and Graphics, null model (red distribution), distribution of expectations created via bootstrapping replacement of 50% of the total available points and 1000 resampling replicates (blue distribution), Table S1: References used to compile the dataset, Table S2: Occurrence sites for <em>P.ficus</em>, Table S3: Correlation analysis of environmental variables for pest, Table S4: ENMeval results for <em>P.ficus</em> from SDMs.</p>
Fig. 15 Oxybelis vittatus. FMNH 170133 in Not withering on the evolutionary vine: systematic revision of the Brown Vine Snake (Reptilia: Squamata: Oxybelis) from its northern distribution
Fig. 15 Oxybelis vittatus. FMNH 170133, from the Canal Zone of Panama. a Profile; b crown; c underside of head
Fig. 14 in Not withering on the evolutionary vine: systematic revision of the Brown Vine Snake (Reptilia: Squamata: Oxybelis) from its northern distribution
Fig. 14 Oxybelis rutherfordi sp. nov. in life. a and b Tobago specimens. JCM; c Aripo Savanna, Trinidad. JCM; d an exceptionally large specimen (2.1 m) from Tobago (M. Patrikeev)
Fig. 12 in Not withering on the evolutionary vine: systematic revision of the Brown Vine Snake (Reptilia: Squamata: Oxybelis) from its northern distribution
Fig. 12 Holotype (UTA R-64851) of Oxybelis rutherfordi sp. nov. in life prior to preserva- tion collected in the Arima Valley, Trinidad (M.G. Rutherford)
Fig. 10 in Not withering on the evolutionary vine: systematic revision of the Brown Vine Snake (Reptilia: Squamata: Oxybelis) from its northern distribution
Fig. 10 Oxybelis microphthalmus in-life. a and b show the profiles while c shows the gaping mouth defensive behavior. Photograph a by JCM and b and c by J. ReyesVelasco
Fig. 9 in Not withering on the evolutionary vine: systematic revision of the Brown Vine Snake (Reptilia: Squamata: Oxybelis) from its northern distribution
Fig. 9 Oxybelis koehleri sp. nov. in life. a Mocorón, Gracias a Dios, Honduras (C.J. Franklin); b Santa Rosa, Costa Rica (L. Porras)
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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.