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535 results for “Stripes”
Fig. 1 in On the distribution of the Himalayan Stripe-necked Snake Liopeltis rappi (Günther, 1860) (Serpentes: Colubridae) in Nepal
Fig. 1. Liopeltis rappi from Dhodeni, Kabilas, Chitwan. Photo Santosh Bhattarai.
Fig. 3 in On the distribution of the Himalayan Stripe-necked Snake Liopeltis rappi (Günther, 1860) (Serpentes: Colubridae) in Nepal
Fig. 3. Habitat of Liopeltis rappi at Dhodeni, Kabilas, Chitwan. Photo Santosh Bhattarai.
Fig. 2 in On the distribution of the Himalayan Stripe-necked Snake Liopeltis rappi (Günther, 1860) (Serpentes: Colubridae) in Nepal
Fig. 2. Distribution of Liopeltis rappi in Nepal.
Figure 1 in First record of F hybrid striped bass (Morone chrysops × Morone saxatilis × Morone chrysops × Morone saxatilis ) in Kemer Dam Lake
Figure 1. Map of Kemer Dam Lake in the western part of Turkey.
Figure 2 in Status and distribution of the Striped Hyaena, Hyaena hyaena, in Turkey: an updated assessment (Carnivora: Mammalia)
Figure 2. Camera trap locations in Muğla province.
Figure 4 in Status and distribution of the Striped Hyaena, Hyaena hyaena, in Turkey: an updated assessment (Carnivora: Mammalia)
Figure 4. The proportions of Striped Hyaena records from Turkey.
Figure 1 in Status and distribution of the Striped Hyaena, Hyaena hyaena, in Turkey: an updated assessment (Carnivora: Mammalia)
Figure 1. Striped Hyaena recorded camera trap locations in Hatay province.
Fig. 38. Character 53, dorsolateral stripe B. State 1 in PHYLOGENETIC SYSTEMATICS OF DART-POISON FROGS AND THEIR RELATIVES (AMPHIBIA: ATHESPHATANURA: DENDROBATIDAE)
Fig. 38. Character 53, dorsolateral stripe B. State 1, present (femoralis, AMNH 140646).
Fig 3 in Western striped squirrel Tamiops mcclellandii: A non-avian sentinel species of bird waves
Fig 3. Close-association between Dicrurus annectens and Tamiops mcclellandii.
Fig. 1 in Western striped squirrel Tamiops mcclellandii: A non-avian sentinel species of bird waves
Fig. 1. Transects and habitat types at the study site.
Fig. 2 in Western striped squirrel Tamiops mcclellandii: A non-avian sentinel species of bird waves
Fig. 2. Close-association between Dicrurus paradiseus and Tamiops mcclellandii.
FIGURE 9 in Systematics and Taxonomy of Great Striped-Faced Bats of the Genus Vampyrodes Thomas, 1900 (Chiroptera: Phyllostomidae)
FIGURE 9. Lateral views of the skulls and lower jaw of (A) Vampyrodes carac-
FIGURE 1 in Systematics and Taxonomy of Great Striped-Faced Bats of the Genus Vampyrodes Thomas, 1900 (Chiroptera: Phyllostomidae)
FIGURE 1. Photograph of an adult male Vampy-
FIGURE 2 in Systematics and Taxonomy of Great Striped-Faced Bats of the Genus Vampyrodes Thomas, 1900 (Chiroptera: Phyllostomidae)
FIGURE 2. Photo-
Genomic data resolve long-standing uncertainty by distinguishing white marlin (Kajikia albida) and striped marlin (K. audax) as separate species
<p>Large pelagic fishes are often broadly and continuously distributed and capable of long-distance movements. These factors can promote gene flow that makes it difficult to disentangle intra- vs. inter-specific levels of genetic differentiation. Here, we assess the relationship of two istiophorid billfishes, white marlin (<em>Kajikia</em> <em>albida</em>) and striped marlin (<em>K</em>. <em>audax</em>), presently considered sister species inhabiting separate ocean basins. Previous studies report levels of genetic differentiation between white marlin and striped marlin that are <a>smaller</a> than those observed among populations of other istiophorid species. To determine whether white marlin and striped marlin comprise separate species or populations of a single globally distributed species, we surveyed 2<a>520</a> single nucleotide polymorphisms (SNPs) in 62 white marlin and 242 striped marlin sampled across the Atlantic, Pacific, and Indian oceans. Multivariate analyses resolved white marlin and striped marlin as distinct groups, and a species tree composed of separate lineages was strongly supported over a single lineage tree. Genetic differentiation between white marlin and striped marlin (<em>F</em><sub>ST</sub> = 0.5384) was also substantially larger than between populations of striped marlin (<em>F</em><sub>ST</sub> = 0.0192–0.0840), and we identified SNPs that allow unambiguous species identification. Our findings indicate that white marlin and striped marlin comprise separate species, which we estimate diverged at approximately 2.38 Mya.</p>
The role of high-contrast male facial stripes in mitigating female aggression in the jumping spider, Plexippus paykulli
<p>Vibrant male coloration and energetic courtship displays set jumping spiders apart from most arachnids, which typically rely on non-visual stimuli. Like many other spiders, female salticids engage in sexual cannibalism, making courtship a risky but necessary endeavor for males. In this study, we investigated the relationship between male coloration and female aggression to better understand the interplay of attraction and aversion during courtship.</p> <p>Many male jumping spiders sport conspicuous coloration or high-contrast patterns that are reminiscent of the coloration of many aposematic insects. The faces of <em>Plexippus paykulli</em> males are adorned with bold vertical stripes they direct toward females during courtship. We hypothesized that these stripes could function as a sensory trap, leveraging female aversion to the signal to reduce the likelihood of cannibalism.</p> <p>We tested whether spiders exhibit an aversion to stripes in the context of predation by manipulating prey coloration and testing spider preference for prey based on the presence or absence of stripes. Then we conducted two courtship experiments by manipulating male facial coloration to determine whether the presence of male stripes affects female aggression and likelihood of mating. We also manipulated female foraging drive in each courtship experiment (either diet or mating status) to see whether common sources of natural variation among females influenced response to courting males. We found that spiders showed an aversion to stripes while foraging but that this aversion does not confer reduced aggression from females toward striped males vs. males with stripes obscured. However, stripes did affect the likelihood of male reproductive success, as striped males mounted females more frequently than non-striped males. Finally, female condition influenced female response to courting males, with hungrier females showing higher aggression and previously mated females being mounted less frequently than non-mated females.</p>
QTL mapping for seedling and adult plant resistance to stripe and leaf rust in two winter wheat populations
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Comparative migration ecology of striped bass and Atlantic sturgeon in the US Southern Mid-Atlantic Bight flyway
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Differential effects of foraging strategies on carotenoid-derived plumage color and individual quality in stripe-tailed yellow finches
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Genomic data resolve long-standing uncertainty by distinguishing white marlin (Kajikia albida) and striped marlin (K. audax) as separate species
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OpenNeuro
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