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138 results for “whiptail”
Fig. 2 in Hybridization Between the Endangered Unisexual Gray-Checkered Whiptail Lizard (Aspidoscelis dixoni) and the Bisexual Western Whiptail Lizard (Aspidoscelis tigris) in Southwestern New Mexico
Fig. 2. Cherry array with drift fence and pitfall traps, where one of the hybrids was found, Antelope Pass, Peloncillo Mountains, Hidalgo County, New Mexico. Photo by C.J.C., June 8, 1990.
Fig. 8 in Hybridization Between the Endangered Unisexual Gray-Checkered Whiptail Lizard (Aspidoscelis dixoni) and the Bisexual Western Whiptail Lizard (Aspidoscelis tigris) in Southwestern New Mexico
Fig. 8. Pattern of morphological distinctiveness expressed by the distribution of canonical variate scores derived from a canonical variate analysis of five meristic characters of 30 specimens of Aspidoscelis from Antelope Pass, Hidalgo County, New Mexico. The specimens include representatives of two species (A. dixoni C and A. t. punctilinealis) and hybrids between them. Note that the three hybrids cluster most closely to their maternal parent.
Data from: Understanding species boundaries that arise from complex histories: Gene flow across the speciation continuum in the spotted whiptail lizards
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FIGURE 3 in A new species of whiptail stingray of the genus Dasyatis Rafinesque, 1810 from the Southwestern Atlantic Ocean (Chondrichthyes: Myliobatiformes: Dasyatidae)
FIGURE 3: Dasyatis colarensis n. sp., UERJ 2006, paratype, male, 530 DW. Dorsal view.
Fig. 35 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones
Fig. 35. Ventral views of the same lizards arranged in the same sequence as in figure 34.
Fig. 3. The contact region. Numbers designate collecting sites. Compare with figure 49 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones
Fig. 3. The contact region. Numbers designate collecting sites. Compare with figure 49.
FIGURE 15 in Laboratory Hybridization among North American Whiptail Lizards, Including Aspidoscelis inornata arizonae × A. tigris marmorata (Squamata: Teiidae), Ancestors of Unisexual Clones in Nature
FIGURE 15. The oviduct (part) and ovary of laboratory hybrid AMNH
FIGURE 14 in Laboratory Hybridization among North American Whiptail Lizards, Including Aspidoscelis inornata arizonae × A. tigris marmorata (Squamata: Teiidae), Ancestors of Unisexual Clones in Nature
FIGURE 14. Volume of the adrenal gland compared to the snout-vent length (SVL)
FIGURE 17 in Laboratory Hybridization among North American Whiptail Lizards, Including Aspidoscelis inornata arizonae × A. tigris marmorata (Squamata: Teiidae), Ancestors of Unisexual Clones in Nature
FIGURE 17. Mesonephros of laboratory hybrid
FIGURE 10 in Laboratory Hybridization among North American Whiptail Lizards, Including Aspidoscelis inornata arizonae × A. tigris marmorata (Squamata: Teiidae), Ancestors of Unisexual Clones in Nature
FIGURE 10. Testis, adrenal gland,
FIGURE 4 in Laboratory Hybridization among North American Whiptail Lizards, Including Aspidoscelis inornata arizonae × A. tigris marmorata (Squamata: Teiidae), Ancestors of Unisexual Clones in Nature
FIGURE 4. Three Aspidoscelis of
FIGURE 3 in Laboratory Hybridization among North American Whiptail Lizards, Including Aspidoscelis inornata arizonae × A. tigris marmorata (Squamata: Teiidae), Ancestors of Unisexual Clones in Nature
FIGURE 3. Parents of the Aspidoscelis hybrids
FIGURE 16 in Laboratory Hybridization among North American Whiptail Lizards, Including Aspidoscelis inornata arizonae × A. tigris marmorata (Squamata: Teiidae), Ancestors of Unisexual Clones in Nature
FIGURE 16. The testis of laboratory
Fig. 9 in Hybridization Between the Endangered Unisexual Gray-Checkered Whiptail Lizard (Aspidoscelis dixoni) and the Bisexual Western Whiptail Lizard (Aspidoscelis tigris) in Southwestern New Mexico
Fig. 9. Antelope Pass, Peloncillo Mountains, Hidalgo County, New Mexico. Photo by C.W.P., April 1,
Whiptail lizards (Aspidoscelis exsanguis) recognize invertebrate prey via cuticular hydrocarbons
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FIGURE 6 in A new species of whiptail stingray of the genus Dasyatis Rafinesque, 1810 from the Southwestern Atlantic Ocean (Chondrichthyes: Myliobatiformes: Dasyatidae)
FIGURE 6: Dasyatis colarensis n. sp. Schematic drawing of the right clasper of holotype in dorsal view. Abbreviations: mts, medial terminal margin serrae; hyp, hypopyle; pe, pent.
FIGURE 5 in A new species of whiptail stingray of the genus Dasyatis Rafinesque, 1810 from the Southwestern Atlantic Ocean (Chondrichthyes: Myliobatiformes: Dasyatidae)
FIGURE 5: Dasyatis colarensis n. sp., UERJ 2006, paratype. Detail of mouth showing the coloration of the lower lip margin.
FIGURES 1–2. Dasyatis colarensis n in A new species of whiptail stingray of the genus Dasyatis Rafinesque, 1810 from the Southwestern Atlantic Ocean (Chondrichthyes: Myliobatiformes: Dasyatidae)
FIGURES 1–2. Dasyatis colarensis n. sp, MNRJ 25179, holotype, male, 630 DW. 1, dorsal view; 2, ventral view.
Parthenogenesis doubles the rate of amino acid substitution in Whiptail mitochondria
<p class="MsoNormal"><span>Sexual reproduction is ubiquitous in the natural world, suggesting that sex must have extensive benefits to overcome the cost of males compared to asexual reproduction. One hypothesized advantage of sex with strong theoretical support is that sex plays a role in removing deleterious mutations from the genome. Theory predicts that transitions to asexuality should lead to the suppression of recombination and segregation and, in turn, weakened natural selection, allowing for the accumulation of slightly deleterious mutations. We tested this prediction by estimating the d<em>N</em>/d<em>S</em> ratios in asexual vertebrate lineages in the genus <em>Aspidoscelis</em> using whole mitochondrial genomes from seven asexual and five sexual species. We found higher d<em>N</em>/d<em>S</em> ratios in asexual <em>Aspidoscelis </em>species, indicating that asexual whiptails accumulate non-synonymous substitutions due to weaker purifying selection. Additionally, we estimated nucleotide diversity and found that asexuals harbor significantly less diversity. Thus, despite their recent origins, slightly deleterious mutations accumulated rapidly enough in asexual lineages to be detected. We provided empirical evidence to corroborate the connection between asexuality and increased </span><span>amino acid substitutions</span><span> in asexual vertebrate lineages.</span></p> <p class="MsoNormal"><span> </span></p>
FIGURE 7. A in Rineloricaria quilombola: a new species of whiptail catfish (Siluriformes, Loricariidae, Loricariinae) from upper and middle Tocantins River basin, Brazil
FIGURE 7. A. Ribeirão Taquaruçuzinho, type locality of Rineloricaria quilombola. and B. ribeirão São João, at Porto Nacional, TO.
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