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Fig. 11 a–d in Not withering on the evolutionary vine: systematic revision of the Brown Vine Snake (Reptilia: Squamata: Oxybelis) from its northern distribution
Fig. 11 a–d Holotype of Oxybelis potosiensis Taylor 1941 (UIMNH 25069) from San Luis Potosí, Mexico; a whole specimen; b the crown, note the lack of a constriction anterior to the eyes, rostral not visible from above, and the relatively broad snout; c the profile; d arrangement of the chin shields
Fig. 8 in Not withering on the evolutionary vine: systematic revision of the Brown Vine Snake (Reptilia: Squamata: Oxybelis) from its northern distribution
Fig. 8 Holotype of Oxybelis koehleri sp. nov., UTA R-46846 preserved; a dorsal; b top of the head; c profile; d ventral views. Scale bar = 1 cm
Fig. 7 in Not withering on the evolutionary vine: systematic revision of the Brown Vine Snake (Reptilia: Squamata: Oxybelis) from its northern distribution
Fig. 7 Specimen of O. aeneus (FMNH 64417) from Manaus, Amazonas, Brazil. This specimen was collected c. 518 km from the type locality
Fig. 4 in Not withering on the evolutionary vine: systematic revision of the Brown Vine Snake (Reptilia: Squamata: Oxybelis) from its northern distribution
Fig. 4 Plot of discrimination analysis of sixteen morphological characters, showing clustering among geographically defined groups. Colors represent specimens from Central America (CA, orange), Central Brazil (CB, black stars), Eastern Mexico (EM, blue), northern South America (NSA, purple), Panama (P, yellow), and western region (WR, green). Colors correspond to those in Fig. 3
Fig. 5 in Not withering on the evolutionary vine: systematic revision of the Brown Vine Snake (Reptilia: Squamata: Oxybelis) from its northern distribution
Fig. 5 Phylogenetic estimate of relationships within Oxybelis estimated from a Bayesian 50% majority-rule consensus phylogram using a multilocus dataset (cyt b, ND4, 12S, 16S, cmos and PRLR; total of 3663 bp) with posterior probabilities (≥ 95) represented at the node (red circles). Values adjacent to nodes represent additional support values (SH-aLRT> 80% and UFboot> 95%) from maximum likelihood (ML)
Fig. 2 in Not withering on the evolutionary vine: systematic revision of the Brown Vine Snake (Reptilia: Squamata: Oxybelis) from its northern distribution
Fig. 2 Image showing the variability in snout shape among populations of Oxybelis aeneus. a A slender taper from the occipital region to rostral scale (UAZ 16787, Arizona, USA); b tapered, but snout in front of eyes is slightly constricted (FMNH 64417, Brazil); c a taper from the occipital region but the area in front of the eyes is broad and the rostal is rounded (UIMNH 25069, San Luis Potosí, Mexico)
Fig. 3 in Not withering on the evolutionary vine: systematic revision of the Brown Vine Snake (Reptilia: Squamata: Oxybelis) from its northern distribution
Fig. 3 Localities from which we obtained tissues for molecular work, other than the type locality represented by a black circle. Colors represent tissues of brown vine snakes from Central America (orange), Eastern Mexico (light blue), Panama (yellow), northern South America (purple), and the western region (light green); other taxa with molecular data represented are O. brevirostris (dark green), O. fulgidus (gray and
Fig. 1 in Not withering on the evolutionary vine: systematic revision of the Brown Vine Snake (Reptilia: Squamata: Oxybelis) from its northern distribution
Fig. 1 In life photographs of Oxybelis aeneus (sensu Keiser 1974) from throughout its distribution showing tremendous morphological variation. a Reserva Amazonica, Peru (W.E. Duellman); b Santa Rosa, Costa Rica (L. Porras); c Venezuela (D.A. Briceño C.); d Jalapão, Tocantins, Brazil (LJV). Photos a and d show a gaping mouth that is a typical defense behavior for members of the Oxybelis aeneus complex
Data from: Rainfall seasonality predicts the germination behaviour of a tropical dry-forest vine
Seed dormancy is considered an adaptive strategy in seasonal and/or unpredictable environments because it prevents germination during climatically favourable periods that are too short for seedling establishment. Tropical dry forests are seasonal environments where seed dormancy may play an important role in plant resilience and resistance to changing precipitation patterns. We studied the germination behaviour of seeds from six populations of the Neotropical vine Dalechampia scandens (Euphorbiaceae) originating from environments of contrasting rainfall seasonality. Seeds produced by second greenhouse-generation plants were measured and exposed to a favourable wet environment at different time intervals after capsule dehiscence and dispersal. We recorded the success and the timing of germination. All populations produced at least some dormant seeds, but seeds of populations originating from more seasonal environments required longer periods of after-ripening before germinating. Within populations, larger seeds tended to require longer after-ripening periods than did smaller seeds. These results indicate among-population genetic differences in germination behaviour and suggest that these populations are adapted to local environmental conditions. They also suggest a role of seed size in germination timing within populations. Ongoing changes in seasonality patterns in tropical dry forests may impose strong selection on these traits.
Figure 1 in Ooencyrtus marcelloi sp. nov. (Hymenoptera: Encyrtidae), an egg parasitoid of Heliconiini (Lepidoptera: Nymphalidae: Heliconiinae) on passion vines (Malpighiales: Passifloraceae) in Central America
Figure 1. Ooencyrtus marcelloi sp. nov. Guerrieri and Noyes. Female: (A) antenna; (B) mandible; (C) base of forewing; (D) hypopygium; (E) ovipositor. Male (F) antenna; (G) genitalia.
Vine Trunk Image/Annotation Dataset
<p><strong>DS_AG_39</strong> VineSet - Vine Trunk Image/Annotation Dataset<br> - RGB images<br> - Thermal images<br> - Infrablue filtered images<br> vineset.zip / 1.1Gb / Images and Annotations</p>
FIGURE 2. A-H. Aeschynanthus rejieae. A. Axillary inflorescence. B in Aeschynanthus rejieae (Gesneriaceae), a new species of lipstick vine from Tawi- Tawi, Philippines
FIGURE 2. A-H. Aeschynanthus rejieae. A. Axillary inflorescence. B. Top view of flower showing the corolla mouth and lobes. C. Flower D. Longitudinal corolla section E. Longitudinal calyx section showing internal hirsute indumentum and ciliate ovary. F. Filament with glandular cilia (white arrow) G. Leaf H. Leaf base showing the persistent sparse pubescence. Photos by Shiella Mae Olimpos.
FIGURE 1 in Aeschynanthus rejieae (Gesneriaceae), a new species of lipstick vine from Tawi- Tawi, Philippines
FIGURE 1. Map of Tawi-Tawi Island showing the surveyed area (dot) in Busay, Barangay Magsagaw within the Municipality of Panglima Sugala. Map by Andrew Ross Reintar.
FIGURE 3. A-E. Aeschynanthus rejieae illustration. A in Aeschynanthus rejieae (Gesneriaceae), a new species of lipstick vine from Tawi- Tawi, Philippines
FIGURE 3. A-E. Aeschynanthus rejieae illustration. A. Habit with details of leaf indumentum. B. Inflorescence. C. Calyx tube longitudinal section with pistil. D. Corolla (split ventrally). E. Front view showing details of the corolla lobes and stamens. Illustrated by Jayson Mansibang.
Fig. 4. GLP-1 in Cucurbitane-type triterpenoids from the vines of Momordica charantia and their anti-inflammatory, cytotoxic, and antidiabetic activity
Fig. 4. GLP-1 secretory effects of compounds 1, 3, and 7 in STC-1 cells. GLP-1 secretory response under each condition was illustrated. Rutin (25 μg/mL) is positive control. Data represent Means ± SEM (n = 4). ***P <0.001, compared with None.
Fig. 2. 2D in Cucurbitane-type triterpenoids from the vines of Momordica charantia and their anti-inflammatory, cytotoxic, and antidiabetic activity
Fig. 2. 2D-NMR correlations of the isolated cucurbitanes. (A) 1H–1H COSY and key HMBC correlations of compounds 1, 4, 5, and 6. (B) Main NOESY correlations of compounds 1, 2, 6, and 7.
Data from: Hybridization and adaptation to introduced balloon vines in an Australian soapberry bug
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Data from: Using multiple traits to assess the potential of introduced and native vines to proliferate in a tropical region
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Data from: Multilocus phylogenetics of new world milkweed vines (Apocynaceae, Asclepiadoideae, Gonolobinae)
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Data from: Euglossine bees mediate only limited long-distance gene flow in a tropical vine
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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.