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297 results for “stress tolerance”
Historical exposure to chemicals reduces tolerance to novel chemical stress in Daphnia (waterflea)
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Data from: A seascape genetic analysis of a stress-tolerant coral species along the Western Australian coast
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Thermal tolerance plasticity and dynamics of thermal tolerance in Eublepharis macularius: Implications for future climate-driven heat stress
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Data from: Plastic and evolutionary responses to heat stress in a temperate dung fly: negative correlation between basal and induced heat tolerance?
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Data from: Temporally autocorrelated environmental fluctuations inhibit the evolution of stress tolerance
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Data from: Evolutionary constraint on low elevation range expansion: Defense‐abiotic stress‐tolerance trade‐off in crosses of the ecological model Boechera stricta
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Data from: Experimental evaluation of the robustness of the growth-stress tolerance trade-off within the perennial grass Dactylis glomerata
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Banks grass mite (Acari: Tetranychidae) suppression may add to the benefit of drought-tolerant corn hybrids exposed to water-stress
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Is drought tolerance a domestication trait in tepary bean?: Allelic diversity at abiotic stress responsive genes in cultivated Phaseolus acutifolius A. Gray and its wild relatives
<p>Some of the major impacts of climate change are expected in the poorest regions of the world where drought stress and nutrient deficiency are already a main issue. Legumes are an essential food crop for the poorest because of their high dietary protein and micronutrient contents. However, they are generally drought susceptible. Therefore, our goal in this study was to explore allele diversity at abiotic stress responsive candidate genes in the only drought tolerant cultivated bean species of the genus <i>Phaseolus</i>, tepary bean (<i>P. acutifolius</i> A. Gray) and its related species <i>P. parvifolius </i>Freytag. Specifically, we estimated drought tolerance in 52 tepary bean <i>s.l.</i> geo-referenced germplasm accessions from the <i>P. acutifolius</i>–<i>parvifolius</i> clade using climate information, and used this estimated drought stress index to examine allele correlations with <i>Asr2</i>, <i>Dreb2B</i> and ERECTA-encoding candidate genes for drought tolerance. Genetic clustering showed that cultivated and wild <i>P. acutifolius</i> were intermingled with <i>P. acutifolius </i>var.<i> tenuifolius</i> and <i>P. parvifolius</i>, signifying that allele diversity at candidate genes for drought tolerance was not scarce in tepary bean <i>s.l</i>. <i>Dreb2B</i> and ERECTA-encoding genes harbored signatures of directional/purifying selection, likely in favor of adaptive alleles selectively advantageous because each had two SNPs significantly correlated (<i>p-value</i> < 0.05) with habitat drought stress at six and 12 months. These results suggest that tepary bean <i>s.l. </i>is a reservoir of novel alleles at candidate genes for drought tolerance, as expected for a drought-tolerant species that originated in warmer and arid environments. Abiotic stress responsive candidate genes also exhibit comparable patterns of selective signatures when comparing orthologous across species, which speaks for a predominant role of gene sub-functionalization likely due to ecological constrains. Our study therefore corroborates that the candidate gene approach is still an effective alternative for marker validation across a broader genetic basis of germplasm accessions. Further efforts to determine the genetic architecture of drought tolerance will unlock novel alleles hidden in a crop with limited modern relevance as tepary bean, but capable of acting as a donor in backcrossing and genome editing strategies with elite common bean lines aiming to meet the imminent demands of a drier world.</p>
Are juveniles as tolerant to salinity stress as adults?: A case study of Northern European, Ponto-Caspian and North American species
<p><span><span><span><span><span><span><span><span><span><span><span><b>Aim: </b>Global biodiversity and ecosystems are highly impacted by anthropogenic activities, such as climate change and introduction of non-indigenous species. As numerous species from the Ponto-Caspian region have established in the North and Baltic Seas, as well as in the Laurentian Great Lakes, there have been large number of studies examining environmental tolerance of these species to determine their future potential to spread. However, many of those studies were conducted only on adult stages, while neglecting the possibility that early life history stages might not be equally resilient. </span></span></span></span></span></span></span></span></span></span></span></p> <p><span><span><span><span><span><span><span><span><span><span><span><b>Location: </b>Northern European, Ponto‐Caspian and North American regions.</span></span></span></span></span></span></span></span></span></span></span></p> <p><span><span><span><span><span><span><span><span><span><span><span><b>Methods: </b>To determine if juveniles would demonstrate the same environmental tolerance as their parents, we examined the salinity tolerance of adults and juveniles of one Northern European (<i>Gammarus salinus</i>), one Ponto-Caspian (<i>Pontogammarus maeoticus</i>) and one North American species (<i>Gammarus tigrinus</i>). Additionally, we compared our study to that of Paiva et al. (2018), who tested the salinity tolerance of the same species using only adults. </span></span></span></span></span></span></span></span></span></span></span></p> <p><span><span><span><span><span><span><span><span><span><span><span><b>Results: </b>Our study determined that both adults and juveniles of all three species tolerated wide ranges of salinity, with juveniles of <i>G. salinus</i> tolerating only slightly narrower salinity range than their parents, while those of <i>P. maeoticus</i> and <i>G. tigrinus</i> much narrower range. Additionally, we determined better survival and higher growth rates of juveniles of <i>G. salinus</i> in higher salinities, and better survival of <i>P. maeoticus</i> in lower salinities. </span></span></span></span></span></span></span></span></span></span></span></p> <p><b>Main conclusions:</b><span><span><span><span><span><span><span><span><span><span> Based on juvenile salinity tolerance, our study further supported findings of Paiva et al. (2018), where Northern European species may be adapted to marine, while Ponto-Caspian to lower saline and freshwater environments. The North American species is probably adapted to intermediate salinities. </span></span></span></span></span></span></span></span></span></span><span><span><span><span><span><span><span><span><span><span>As juveniles do not tolerate the same salinity stress as adults,</span></span></span></span></span></span></span></span></span></span><span><span><span><span><span><span><span><span><span><span> we emphasize the importance of testing all life-history stages when predicting species resilience to environmental stressors.</span></span></span></span></span></span></span></span></span></span></p>
Data from: A positive genetic correlation between hypoxia tolerance and heat tolerance supports a controversial theory of heat stress
We used quantitative genetics to test a controversial theory of heat stress, in which animals overheat when the demand for oxygen exceeds the supply. This theory, referred to as oxygen- and capacity-limited thermal tolerance, predicts a positive genetic correlation between hypoxia tolerance and heat tolerance. We demonstrate the first genetic correlation of this kind in a model organism, Drosophila melanogaster. Genotypes more likely to fly under hypoxic stress (12% O2) were also more likely to fly under heat stress (39°C). This finding prompts new questions about mechanisms and limits of adaptation to heat stress.
Limitations of plant stress tolerance upon heat and CO2 exposure in black ploplar: Assessment of photosynthetic traits and stress volatile emissions
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Long term environmental stability drives reduced stress tolerance in salt lake invertebrates
<p>The capacity of species to tolerate physical stressors is critical in a world of increasing environmental instability, however, past selective environments should dramatically impact on future stress tolerance, particularly in isolated populations. Through stabilising selection, long-term environmental stasis may reduce physiological tolerance, creating an evolutionary legacy where populations are less fit if environments change. Few empirical studies have investigated this evolutionary legacy of past selection, and of particular interest whether stabilising selection in a benign environment reduces stress tolerance in natural systems. Here we use multiple populations of salt-lake invertebrates (<i>Coxiella striata, Austrochiltonia subtenuis</i>) with either stable or fluctuating environmental histories to investigate the relationship between stabilising selection and environmental stress resistance. Tolerance to both salinity and temperature stress were examined in invertebrate populations from lakes with long-term (decadal) stable environments and compared with populations from lakes with extreme salinity variations. Individuals from stable environments demonstrated significantly lower survival under both increasing salinity and temperature stresses when compared with environmentally unstable populations. Our results support the hypothesis that the evolutionary legacy from stabilising selection in constant environments leads to reduced stress tolerance. This finding demonstrates that under an increasingly variable climate, the evolutionary legacies of populations will be critical for future survival and adaptation.</p>
Figure 2 in Antioxidant status and their enhancements strategies for water stress tolerance in chickpea
Figure 2. (a) Influence of exogenous application of osmoprotectants on relative growth rate (g g-1 day-1) of chickpea genotypes in Bahawalpur; (b) Influence of exogenous application of osmoprotectants on relative growth rate (g g-1 day-1) of chickpea genotypes in Cholistan. Whereas D1= well watered; D2= Drought at flowering+ pod formation + grain filling stage; D3= Drought at flowering stage; DAS, Days after sowing.
Biostimulants MTU® and pidolic acid have complementary roles in the improvement of stress tolerance, nutrient use efficiency and yield in arable crops
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Table 1 in Improvement of Pisum sativum salt stress tolerance by bio-priming their seeds using Typha angustifolia leaves aqueous extract
<p><b>Table 1</b> Germination percentage (%G) and germination index (GI) of not primed (NP) and primed (P) pea seeds, in presence of 0, 240, and 320 mM NaCl.</p><table><tbody><tr><th>NaCl (mM)</th><th>Seeds</th><th>% G</th><th>GI</th></tr></tbody><tbody><tr><th>0</th><td>NP</td><td>100a</td><td>5.22b</td></tr><tr><td>P</td><td>100a</td><td>6.72a</td></tr><tr><th>240</th><td>NP</td><td>51.25c</td><td>1.89d</td></tr><tr><td>P</td><td>66.25b</td><td>2.57c</td></tr><tr><th>320</th><td>NP</td><td>0e</td><td>0f</td></tr><tr><td>P</td><td>10d</td><td>0.33e</td></tr></tbody></table><p>Means with the same letters in a column are not significantly different at p <0.05.</p>
Screening the TOMRES collection for combined stress tolerance in Northern European glasshouse conditions
<p>These experiments assessed varietal yield and quality in response to a combined treatment of reduced N and P application and severe water limitation (Combined stress) when grown in rockwool substrates. <br> Data was collection to assess relative NUE of varieties under treatment and control conditions as well as the physiological performance and fruit quality characteristics of varieties in order to contribute to a ranking for combined stress. </p> <p>Two trials were carried out (February - May 2019 and June - September 2019) at the Stockbridge Technology Centre in North Yorkshire, UK. </p>
Evolution of sex-specific heat stress tolerance and larval Hsp70 expression in populations of Drosophila melanogaster adapted to larval crowding
<p class="BodyA">The ability to tolerate temperature stress is an important component of adult fitness. In holometabolous insects like <i>Drosophila melanogaster,</i> adult stress resistance can be affected by growth conditions experienced during the larval stages. While evolution under crowded larval conditions is known to lead to the correlated evolution of many adult traits, its consequences on adult heat stress tolerance have not been investigated. Therefore, in the present study, we assessed the adult heat stress tolerance in populations of <i>D.</i><i> </i><i>melanogaster</i> adapted to a stressful larval crowding environment. We used replicate populations of <i>D.</i><i> </i><i>melanogaster</i>, selected for adaptation to larval crowding stress (MCUs), for more than 230 generations, and their respective controls (MBs). Larvae from selected and control populations were grown under crowded and uncrowded conditions and their adult heat shock resistance at two different temperatures was measured. Further, we compared Hsp70 expression in crowded and uncrowded larvae of both populations and also measured the Hsp70 expression after a mild-heat treatment in adults of selected and control populations. Our results showed that adaptation to larval crowding leads to the evolution of Hsp70 gene expression in larval stages and improves adult heat-stress tolerance ability in males, but not in females. </p>
Fig. 2 in Transcriptome profiling of two Dactylis glomerata L. cultivars with different tolerance in response to submergence stress
Fig. 2. Venn diagram of differentially expressed genes (DEGs).
Safety and Tolerability of Psilocybin in Post-Traumatic Stress Disorder
ClinicalTrials.gov study NCT05562973. IPD Sharing: NO. Countries: 0. Publications: 1.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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