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1,014 results for “TIGER”
Figure 1. Amerila spp. from Flores Island, Indonesia. A-D A in A review of the tiger moth genus Amerila Walker, 1855 from Flores Island, Indonesia, with a description of a new species (Lepidoptera: Erebidae: Arctiinae)
Figure 1. Amerila spp. from Flores Island, Indonesia. A-D A. rosenfeldae sp. nov.: A) male upperside (holotype); B) female upperside (paratype); C) male underside (holotype); D) female underside (paratype). E-F A. astreus: E) male upperside; F) female upperside. Scale bar = 10 mm. (Photos: Vitaly M. Spitsyn).
Figure 6 in A review of tiger moths (Lepidoptera: Erebidae: Arctiinae: Arctiini) from Flores Island, Lesser Sunda Archipelago, with description of a new species and new subspecies
Figure 6. Fifty-percent majority-rule consensus phylogenetic tree of Spilarctia spp. and related taxa recovered from Bayesian analysis with 26 in-group COI haplotypes (see Table 2 for details). A haplotype of Theretra natashae was used as an out-group. Black numbers near branches are Bayesian posterior probabilities. The scale bar indicates branch lengths (nucleotide substitutions per site).
Figure 4 in A review of tiger moths (Lepidoptera: Erebidae: Arctiinae: Arctiini) from Flores Island, Lesser Sunda Archipelago, with description of a new species and new subspecies
Figure 4. Spilarctia mikeli sp. nov., ♀ holotype from Flores Island, Lesser Sundas, Indonesia (RMBH, voucher no. Sph0695): A) upperside; B) underside. Scale bar: 10 mm. Photos: Vitaly M. Spitsyn.
Figure 2 in A review of tiger moths (Lepidoptera: Erebidae: Arctiinae: Arctiini) from Flores Island, Lesser Sunda Archipelago, with description of a new species and new subspecies
Figure 2. Examples of Arctiini species from Flores Island, Lesser Sundas, Indonesia: A) Euchromia horsfieldi (Moore, 1859), ♀ (Sph0723); B) Utetheisa pulchelloides Hampson, 1907, ♀ (RMBH, voucher no. Sph0717); C) Amerila astreus (Drury, 1773), ♀ (RMBH, voucher no. Sph0694); D) A. astreus, ♂ (RMBH, voucher no. Sph0693); E) Nyctemera baulus (Boisduval, 1832), ♂ (RMBH, voucher no. Sph0720); F) N. baulus, ♀ (RMBH, voucher no. Sph0721); G) Creatonotos gangis (Linnaeus, 1763), ♂ (RMBH, voucher no. Sph0595); H) Lemyra maculifascia (Walker, 1855), ♂ (RMBH, voucher no. Sph0722). Scale bar: 10 mm. Photos: Vitaly M. Spitsyn.
Figure 1 in A review of tiger moths (Lepidoptera: Erebidae: Arctiinae: Arctiini) from Flores Island, Lesser Sunda Archipelago, with description of a new species and new subspecies
Figure 1. Map of the study region. The red ball indicates West Flores, the type locality of Spilarctia mikeli sp. nov. and Aloa cardinalis danau ssp. nov. The base of the map was modified from Lohman et al. (2011).
Figure 3 in A review of tiger moths (Lepidoptera: Erebidae: Arctiinae: Arctiini) from Flores Island, Lesser Sunda Archipelago, with description of a new species and new subspecies
Figure 3. Aloa cardinalis danau ssp. nov. from Flores Island, Lesser Sundas, Indonesia: A) ♂ holotype (RMBH, voucher no. Sph0724); B) ♀ paratype (Sph0729). Scale bar: 10 mm. Photos: Vitaly M. Spitsyn.
Assessing hybrid vigor using the thermal sensitivity of physiological trade-offs in tiger salamanders
<ol> <li>Hybridization between species affects biodiversity and population sustainability in numerous ways, many of which depend on the fitness of the hybrid relative to the parental species. Hybrids can exhibit fitter phenotypes compared to the parental lineages, and this 'hybrid vigor' can then lead to the extinction of one or both parental lines.</li> <li>In this study, we analyzed the relationship between water loss and gas exchange to compare physiological performance among three tiger salamander genotypes – the native California tiger salamander (CTS), the invasive barred tiger salamanders (BTS), and CTS x BTS hybrids across multiple temperatures (13.5°C, 20.5°C, and 23.5°C). We developed a new index of performance, the water-gas exchange ratio (WGER), which we define as the ratio of gas exchange to evaporative water loss (µL VO<sub>2</sub>/µL H<sub>2</sub>O). The ratio describes the ability of an organism to support energetically costly activities with high levels of gas exchange while simultaneously limiting water loss to lower desiccation risk. We used flow-through respirometry to measure the thermal sensitivity of metabolic rate and resistance to water loss of each salamander genotype to compare indices of physiological performance.</li> <li>We found that temperature had a significant effect on metabolic rate and resistance to water loss, with both traits increasing as temperatures warmed. Across genotypes, we found that hybrids have a higher WGER than the native CTS, owing to a higher metabolic rate despite having a lower resistance to water loss.</li> <li>These results provide greater insight into the physiological mechanisms driving hybrid vigor and offer a potential explanation for the rapid spread of salamander hybrids. More broadly, our introduction of the WGER may allow for species- or lineage-wide comparisons of physiological performance across changing environmental conditions, highlighting the insight that can be gleaned from multi-trait analysis of organism performance.</li> </ol>
Data on rainforest birds from line transect surveys in the Kalakad - Mundathurai Tiger Reserve, Tamil Nadu, India
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Ancient DNA reveals genetic admixture in China during tiger evolution
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Assessing hybrid vigor using the thermal sensitivity of physiological trade-offs in tiger salamanders
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Data from: Interspecific interactions among major carnivores in Panna Tiger Reserve: A multispecies occupancy approach
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Supporting data for tiger beetle stable isotope analysis
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Data from: Unraveling the genomic diversity and admixture history of captive tigers in the United States
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Convergence test: Double white dwarf merger (Octo-Tiger)
<p>Configuration files to reproduce the simulation for the convergence test.</p> <p> </p> <p>To generate the input files run:</p> <pre><code class="language-bash">octotiger --config_file=rcb_init.init --silo_num_groups=n</code></pre> <p> </p> <p>Octo-Tiger (b4c51431) and following dependencies were used</p> <ul> <li>HPX (1.4.0),</li> <li>hwloc (1.11.1),</li> <li>silo (4.10.2),</li> <li>jemalloc (5.1.0),</li> <li>hdf5 (1.8.12),</li> <li>cray-mpich/MVAPICH2 (7.7.10/2.3.2),</li> <li>gcc (8.3.0),</li> <li>APEX (8ba5090),</li> <li>and Papi (5.7.0)</li> </ul> <p>The Octo-Tiger source code is available on <a href="http://github.com/STEllAR-GROUP/octotiger">Github.</a></p> <p>To run the simulation run:</p> <pre><code class="language-bash">octotiger --config_file=rcb.ini --silo_num_groups=n</code></pre> <p> </p> <p>where n is the number of nodes.</p> <p> </p> <p> </p>
Data from: Development and validation of a RAD-Seq target-capture based genotyping assay for routine application in advanced black tiger shrimp (Penaeus monodon) breeding programs
<p><i><span>Background</span></i></p> <p><span>The development of genome-wide genotyping resources has provided terrestrial livestock and crop industries with the unique ability to accurately assess genomic relationships between individuals, uncover the genetic architecture of commercial traits, as well as identify superior individuals for selection based on their specific genetic profile. Utilising recent advancements in <i>de-novo</i> genome-wide genotyping technologies, it is now possible to provide aquaculture industries with these same important genotyping resources, even in the absence of existing genome assemblies. Here, we present the development of a genome-wide SNP assay for the Black Tiger shrimp (<i>Penaeus monodon</i>) through utilisation of a reduced-representation whole-genome genotyping approach (DArTseq).</span></p> <p><i><span>Results</span></i></p> <p><span>Based on a single reduced-representation library, 31,262 polymorphic SNPs were identified across 650 individuals obtained from Australian wild stocks and commercial aquaculture populations. After filtering to remove SNPs with low read depth, low MAF, low call rate, deviation from HWE, and non-Mendelian inheritance, 7,542 high-quality SNPs were retained. From these, 4,236 high-quality genome-wide loci were selected for bates-probe development and 4,194 SNPs were included within a finalized target-capture genotype-by-sequence assay (DArTcap). This assay was designed for routine and cost effective commercial application in large scale breeding programs, and demonstrates higher confidence in genotype calls through increased call rate (from 80.2 </span>± 14.7 to 93.0% ± 3.5%<span>), </span>increased read depth (from 20.4 ± 15.6 to 80.0 ± 88.7<span>), as well as a 3-fold reduction in cost over traditional genotype-by-sequencing approaches.</span></p> <p><i><span>Conclusion</span></i></p> <p><span>Importantly, this assay equips the <em>P. monodon</em> industry with the ability to simultaneously assign parentage of communally reared animals, undertake genomic relationship analysis, manage mate pairings between cryptic family lines, as well as undertake advance studies of genome and trait architecture. Critically this assay can be cost effectively applied as <em>P. monodon</em> breeding programs transition to undertaking genomic selection.</span></p>
Image 5 in Tiger beetles (Coleoptera: Cicindelidae) of ancient reservoir ecosystems of Sri Lanka
Image 5. Lophyra (Lophyra) catena (x 10 x 1.0)
Figure 1 in Tiger beetles (Coleoptera: Cicindelidae) of ancient reservoir ecosystems of Sri Lanka
Figure 1. Reservoirs of Sri Lanka surveyed for the occurrence of tiger beetles
Image 4 in Tiger beetles (Coleoptera: Cicindelidae) of ancient reservoir ecosystems of Sri Lanka
Image 4. Cylindera (Oligoma) lacunosa (x 10 x 1.5)
Data from: Species-specific spatiotemporal patterns of leopard, lion and tiger attacks on humans
1. Large carnivores of the genus Panthera can pose serious threats to public safety. Although the annual number of attacks on humans is rare compared to livestock depredation, such incidents undermine popular support for wildlife conservation and require immediate responses to protect human life. 2. We used a space-time scan method to perform a novel spatiotemporal analysis of 908 attacks on humans by lions, leopards and tigers to estimate the risks of further attacks in the same locales. 3. We found that a substantial proportion of attacks were clustered in time and space, but the dimension of these outbreaks varied between species. Lion outbreaks included more human fatalities, persisted for longer periods of time, and extended over larger areas than tiger or leopard outbreaks. 4. These techniques could be used by relevant agencies to warn local people of risks from further attacks within a certain time and distance following an initial incident by each species, as well as identify areas that require management interventions to address these threats.31-Oct-2018
Tiger 1 - Worn Tank (2k Textures)
A Tiger 1 tank. 2k Textures included for download. https://www.artstation.com/artwork/b5B1JE Modelled in Blender. Textured in Substance and Blender. I have a set of "clean" textures as well, message me if you're interested. Source: Objaverse 1.0 / Sketchfab
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Allen Brain Atlas
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