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133 results for “thermal plasticity”
Data from: Does local adaptation along a latitudinal cline shape plastic responses to combined thermal and nutritional stress?
<p>Thermal and nutritional stress are commonly experienced by animals. This will become increasingly so with climate change. Whether populations can plastically respond to such changes will determine their survival. Plasticity can vary among populations depending on the extent of environmental heterogeneity. However, theory conflicts as to whether environmental heterogeneity should increase or decrease plasticity. Using three locally-adapted populations of Drosophila melanogaster sampled from a latitudinal gradient, we investigated whether plastic responses to combinations of nutrition and temperature increase or decrease with latitude for four traits: egg-adult viability, egg-adult development time, and two body size traits. Employing nutritional geometry, we reared larvae on 25 diets varying in protein and carbohydrate content at two temperatures: 18ºC and 25ºC. Plasticity varied among traits and across the three populations. Viability was highly canalized in all three populations. The tropical population showed the least plasticity for development time, the sub-tropical showed the highest plasticity for wing area, and the temperate population showed the highest plasticity for femur length. We found no evidence of latitudinal plasticity gradients in either direction. Our data highlight that differences in thermal variation and resource predictability experienced by populations along a latitudinal cline are not sufficient to predict their plasticity. </p>
Datasets: thermal plasticity is independent of environmental history in an intertidal seaweed
<p><span><span><span><span><span><span><span><span><span><span><span>Organisms inhabiting the intertidal zonehave been used to study natural ecophysiological responses and adaptations to thermal stress because these organisms are routinely exposed to high-temperature conditions for hours at a time. While intertidal organisms may be inherently better at withstanding temperature stress due to regular exposure and acclimation, they could be more vulnerable to temperature stress, already living near the edge of their thermal limits. Strong gradients in thermal stress across the intertidal zone present an opportunity to test whether thermal tolerance is a plastic or canalized trait in intertidal organisms. Here, we studied the intertidal pool-dwelling calcified alga, <i>Ellisolandia elongata</i>, under near-future temperature regimes, and the dependence of its thermal acclimatization response on environmental history. Two timescales of environmental history were tested during this experiment. The intertidal pool of origin was representative of long-term environmental history over the alga's life (including settlement and development), while the pool it was transplanted into accounted for recent environmental history (acclimation over many months). Unexpectedly, neither long-term nor short-term environmental history, nor ambient conditions, affected photosynthetic rates in <i>E. elongata</i>. Individuals were plastic in their photosynthetic response to laboratory temperature treatments (mean 13.2°C, 15.7°C, and 17.7°C). Further, replicate ramets from the same individual were not always consistent in their photosynthetic performance from one experimental time point to another or between treatments, and exhibited no clear trend in variability over experimental time. High variability in climate change responses between individuals may indicate the potential for resilience to future conditions, and thus may play a compensatory role at the population or species level over time.</span></span></span></span></span></span></span></span></span></span></span></p>
Data from: Plasticity of thermal tolerance and its relationship with growth rate in juvenile mussels (Mytilus californianus)
Complex life cycles characterized by uncertainty at transitions between larval/juvenile and adult environments could favor irreversible physiological plasticity at such transitions. To assess whether thermal tolerance of intertidal mussels (Mytilus californianus) adjusts to post-settlement environmental conditions, we collected juveniles from their thermally buffered microhabitat from high and low-shore locations at cool (wave-exposed) and warm (wave-protected) sites. Juveniles were transplanted to unsheltered cages at the two low sites or placed in a common garden. Juveniles transplanted to the warm site for one month in summer had higher thermal tolerance, regardless of origin site. In contrast, common-garden juveniles from all sites had lower tolerance indistinguishable from exposed-site transplants. After six months in the field plus a common garden period, there was a trend for higher thermal tolerance at the protected site, while reduced thermal tolerance at both sites indicated seasonal acclimatization. Thermal tolerance and growth rate were inversely related after one but not six months; protected-site transplants were more tolerant but grew more slowly. In contrast to juveniles, adults from low-shore exposed and protected sites retained differences in thermal tolerance after common garden treatment in summer. Both irreversible and reversible forms of plasticity must be considered in organismal responses to changing environments.
Data from: Phenotypic plasticity and the effects of thermal fluctuations on specialists and generalists
<p>Classical theories predict that relatively constant environments should generally favor specialists, while fluctuating environments should select for generalists. However, theoretical and empirical results have pointed out that generalist organisms might on the contrary perform poorly under fluctuations. In particular, if generalism is underlaid by phenotypic plasticity, performance of generalists should be modulated by the temporal characteristics of environmental fluctuations. Here, we used experiments in microcosms and a mathematical model to test whether the period or autocorrelation of thermal fluctuations mediate links between the level of generalism and the performance of organisms under fluctuations. In the experiment, thermal fluctuations consistently impeded performance compared to constant conditions. However, the intensity of this effect depended on the level of generalism: while the more specialists strains performed better under fast or negatively autocorrelated fluctuations, plastic generalists performed better under slow or positively autocorrelated fluctuations. Our model suggests that these effects of fluctuations on organisms' performance may result from a time delay in the expression of plasticity, restricting its benefits to slow-enough fluctuations. This study points out the need to further investigate the temporal dynamics of phenotypic plasticity to better predict its fitness consequences under environmental fluctuations.</p>
Thermal plasticity and evolution shape predator-prey interactions differently in clear and turbid water
<p>Warming and eutrophication negatively affect freshwater ecosystems by modifying trophic interactions and increasing water turbidity. We need to consider their joint effects on predator-prey interactions, and how these depend on the thermal evolution of both predator and prey.</p> <p>We quantified how 4°C warming and algae-induced turbidity (that integrates turbidity per se and increased food for zooplankton prey) affect functional response parameters and prey population parameters in a common-garden experiment. We did so for all combinations of high- and low-latitude predator (damselfly larvae) and prey (water fleas) populations to assess the potential impact of thermal evolution of predators and/or prey at a high latitude under warming using a space-for-time substitution. We then modelled effects on the system stability (i.e. tendency to oscillate) under different warming, turbidity and evolutionary scenarios.</p> <p>Warming and turbidity had little effect on the functional response parameters of high-latitude predators. In contrast, warming and turbidity reduced the handling times of low-latitude predators. Moreover, warming increased the search rates of low-latitude predators in clear water but instead decreased these in turbid water.</p> <p>Warming increased stability (i.e. prevented oscillations) in turbid water (except for the "high-latitude predator & high-latitude prey" system), mainly by decreasing the prey's carrying capacity and partly also by decreasing search rates, while it did not affect stability in clear water. Algae-induced turbidity generally decreased stability, mainly by increasing the prey's carrying capacity and partly also by increasing search rates. This resembles findings that nutrient enrichment can reduce the stability of trophic systems. The expected stability of the high-latitude trophic system under warming was dependent on the turbidity level: our results suggest that thermal plasticity tends to destabilize the high-latitude trophic system under warming in clear water but not in turbid water, and that thermal evolution of the predator will stabilize the high-latitude system under warming in turbid water but less so in clear water.</p> <p>The extent to which thermal plasticity and evolution shape trophic system stability under warming may strongly differ between clear and turbid water bodies, with their contributions having a more stabilizing role in turbid water.</p>
Rapid evolution of thermal tolerance and phenotypic plasticity in variable environments
<p>These are the data and code to go with "<strong>Rapid evolution of thermal tolerance and phenotypic plasticity in variable environments</strong>"</p> <p><strong>Figure 01 takes the following data/scripts:</strong></p> <p><a href="https://zenodo.org/api/files/cc14086e-84ed-4a13-b2d4-cf3cda0d669f/20210610_Thally02_Figure01_plot_and_stats.R">20210610_Thally02_Figure01_plot_and_stats.R </a> with <a href="https://zenodo.org/api/files/cc14086e-84ed-4a13-b2d4-cf3cda0d669f/track_keeper.csv">track_keeper.csv </a> and <a href="https://zenodo.org/api/files/cc14086e-84ed-4a13-b2d4-cf3cda0d669f/corr_Response%20growth%20.csv">corr_Response growth .csv </a>. These files contain growth rates per transfers for all selection environments throughout the experiment and growth rates in correlated environments during reciprocal transplants, respectively. </p> <p><strong>Figure 02 takes the following data/scripts:</strong></p> <p> </p> <p><a href="https://zenodo.org/api/files/cc14086e-84ed-4a13-b2d4-cf3cda0d669f/20210610_Thally02_Figure02_plot_and_stats.R">20210610_Thally02_Figure02_plot_and_stats.R </a> with <a href="https://zenodo.org/api/files/cc14086e-84ed-4a13-b2d4-cf3cda0d669f/20161120_res_logis_t000.csv">20161120_res_logis_t000.csv </a>and <a href="https://zenodo.org/api/files/cc14086e-84ed-4a13-b2d4-cf3cda0d669f/20161123_resloglint300.csv">20161123_resloglint300.csv .</a> These files contain the output of the shapes of the growth curves (i.e. information on lag time , growth at µmax, K etc) for all samples in all selection environments at t0 and t300, respectively</p> <p><strong>The remaining figures - position not clear at time of submission - take the following data/script. </strong></p> <p>For plasticity in FRRF data, the script 20181204_FRRF_plasticity.R takes the FRRF raw data contained in <a href="https://zenodo.org/api/files/cc14086e-84ed-4a13-b2d4-cf3cda0d669f/allfvfmdata_thally_t300_t000.csv">allfvfmdata_thally_t300_t000.csv </a>. Extracted parameters are in files <a href="https://zenodo.org/api/files/cc14086e-84ed-4a13-b2d4-cf3cda0d669f/CvaluesThally02.csv">CvaluesThally02.csv</a>, <a href="https://zenodo.org/api/files/cc14086e-84ed-4a13-b2d4-cf3cda0d669f/psiPSI_slope_intercept.csv">psiPSI_slope_intercept.csv</a>, and <a href="https://zenodo.org/api/files/cc14086e-84ed-4a13-b2d4-cf3cda0d669f/rP_extracted_values.csv">rP_extracted_values.csv </a> and can be analysed using the R script <a href="https://zenodo.org/api/files/cc14086e-84ed-4a13-b2d4-cf3cda0d669f/extracted%20parameter%20plots.R">extracted parameter plots.R .</a> R script <a href="https://zenodo.org/api/files/cc14086e-84ed-4a13-b2d4-cf3cda0d669f/FRRF%20visualisation%20only%20.R">FRRF visualisation only .R </a> is for visualisation only, as the title suggests. </p> <p>For comparing plasticity/growth , the data are in <a href="https://zenodo.org/api/files/cc14086e-84ed-4a13-b2d4-cf3cda0d669f/20170327_giantbigtable.csv">20170327_giantbigtable.csv </a>, and can be visualised/analysed in <a href="https://zenodo.org/api/files/cc14086e-84ed-4a13-b2d4-cf3cda0d669f/plast%20vs%20growth.R">plast vs growth.R </a></p> <p>In order to recreate the AMOVAS based on SNVs, use <a href="https://zenodo.org/api/files/cc14086e-84ed-4a13-b2d4-cf3cda0d669f/all_variants_fixed-only_using_5x_depth_threshold.csv?versionId=01cbf6bf-fe16-4e7d-aae8-58c527596ebb">all_variants_fixed-only_using_5x_depth_threshold.cvs </a> with <a href="https://zenodo.org/api/files/cc14086e-84ed-4a13-b2d4-cf3cda0d669f/amova%20thally02.R?versionId=e9c21378-ee37-4418-9ce1-76db821e645a">amova thally02.R </a></p> <p>For additional information, please contact elisa.schaum@uni-hamburg.de </p>
Plasticity and associated epigenetic mechanisms play a role in thermal evolution during range expansion
<p>Due to global change many species are shifting their distribution and are thereby confronted with novel thermal conditions at the moving range edges. <span>Especially during the initial phases of exposure to a new environment, it has been hypothesized that plasticity and associated epigenetic mechanisms enable species to cope with environmental change.</span> We tested this idea by capitalizing on the well-documented southward range expansion of the damselfly Ischnura elegans from France into Spain where the species has invaded warmer regions in the 1950s in eastern Spain (old edge region) and in the 2010s in central Spain (new edge region). Using a common garden experiment at rearing temperatures matching the ancestral and invaded thermal regimes, we tested for evolutionary changes in (thermal plasticity in) larval life history and heat tolerance in these expansion zones. Through the use of de- and hypermethylating agents we tested whether epigenetic mechanisms play a role in enabling heat tolerance during expansion. We used the phenotype of the native sister species in Spain, I. graellsii, as proxy for the locally adapted phenotype. New edge populations converged towards the phenotype of the native species through plastic thermal responses in life history and heat tolerance while old edge populations (partly) constitutively evolved a faster life history and higher heat tolerance than the core populations, thereby matching the native species. Only the heat tolerance of new edge populations increased significantly when exposed to the hypermethylating agent. This suggests that the DNA methylation machinery is more amenable to perturbation at the new edge and shows it is able to play a role in achieving a higher heat tolerance. Our results show that both (evolved) plasticity as well as associated epigenetic mechanisms are initially important when facing new thermal regimes but that their importance diminishes with time.</p>
Data from: Thermal plasticity in protective wing pigmentation is modulated by genotype and food availability in an insect model of seasonal polyphenism
<p>Phenotypic variation in natural populations results from complex interactions between organisms and their changing environments. The environment shapes both phenotypic frequencies (during adaptation) and organismal phenotypes (through phenotypic plasticity). Developmental plasticity, in particular, refers to the phenomenon whereby an organism's phenotype depends on the environmental conditions during development. It can match phenotype to ecological conditions and help organisms to cope with environmental heterogeneity, including differences between alternating seasons. Experimental studies of developmental plasticity often focus on the impact of individual environmental cues and do not take explicit account of genetic variation. In contrast, natural environments are complex, comprising multiple variables with combined effects that are poorly understood and may vary among genotypes. We investigated the effects of multifactorial environments on the development of the seasonally plastic eyespots of <em>Bicyclus anynana</em> butterflies. Eyespot size depends on developmental temperature and is involved in alternative seasonal strategies for predator avoidance. In nature, both temperature and food availability undergo seasonal fluctuations. However, our understanding of how thermal plasticity in eyespot size varies in response to food availability and across genotypes remains limited. To address this, we investigated the combined effects of temperature (T; two levels: 20°C and 27°C) and food availability (N; two levels: control and limited) during development. We examined their impact on wing and eyespot size in adult males and females from multiple genotypes (G; 28 families). We found evidence of thermal and nutritional plasticity and temperature-by-nutrition interactions (significant TxN) on the size of eyespots in both sexes. Food limitation resulted in relatively smaller eyespots and tempered the effects of temperature. Additionally, we found differences among families for thermal plasticity (significant GxT effects), but not for nutritional plasticity (non-significant GxN effects) nor for the combined effects of temperature and food limitation (non-significant GxTxN effects). Our results reveal the context dependence of thermal plasticity, with the slope of thermal reaction norms varying across genotypes and across nutritional environments. We discuss these results in light of the ecological significance of pigmentation and the value of considering thermal plasticity in studies of the biological impact of climate change.</p>
Interindividual plasticity in metabolic and thermal tolerance traits from populations subjected to recent anthropogenic heating
<p><span><span><span><span><span><span><span><span><span><span>To better understand temperature's role in the interaction between local evolutionary adaptation and physiological plasticity, we investigated acclimation effects on metabolic performance and thermal tolerance among natural <i>Fundulus heteroclitus</i> populations from different thermal environments. <i>F. heteroclitus </i>populations<i> </i>experience large daily and seasonal temperature variations, as well as local mean temperature differences across their large geographic cline. In this study, we focus on three populations: one locally heated (32°C) by thermal effluence (TE) from the Oyster Creek Nuclear Generating Station, NJ and two nearby reference populations that do not experience local heating (28°C). After acclimation to 12°C or 28°C, we quantified whole animal metabolic rate (WAM), critical thermal maximum (CTMax) and substrate specific cardiac metabolic rate (CaM, substrates: glucose, fatty acids, lactate plus ketones plus ethanol, and endogenous [i.e., no added substrates]) in ~160 individuals from these three populations. Populations showed few significant differences due to large interindividual variation within each population and variation in acclimation response within any single trait. In general, for WAM and CTMax the interindividual variation in acclimation response (log<sub>2</sub> ratio 28°C/12°C) was a function of performance at 12°C with greater acclimation response for individuals that had lower 12°C performance. In contrast, for CaM the rates when acclimated and assayed at 12°C or 28°C were nearly identical. The small differences in CaM between 12°C and 28°C temperature were partially explained by cardiac remodeling where individuals acclimated to 12°C had larger hearts than individuals acclimated to 28°C, resulting in a higher CaM rate per unit heart mass at 28°C than 12°C. Correlation among physiological traits were dependent on acclimation temperature. For example, WAM was negatively correlated with CTMax at 12°C but positively correlated at 28°C. Additionally, glucose substrate supported higher cardiac metabolism than fatty acid, and fatty acid supported higher cardiac metabolism than LKA or endogenous. However, these responses were highly variable with some individuals using much more FA than glucose. These data suggest a complex relationship between specific, temperature-dependent physiological traits. </span></span></span></span></span></span></span></span></span></span></p>
Genetic differentiation underlies seasonal variation in thermal tolerance, body size, and plasticity in a short-lived copepod
<p>Organisms experience variation in the thermal environment on several different temporal scales, with seasonality being particularly prominent in temperate regions. For organisms with short generation times, seasonal variation is experienced across, rather than within, generations. How this variation affects the seasonal evolution of thermal tolerance and phenotypic plasticity is understudied, but has direct implications for the thermal ecology of these organisms. Here we document intra-annual patterns of thermal tolerance in two species of Acartia copepods (Crustacea) from a highly seasonal estuary, showing strong variation across the annual temperature cycle. Common garden, split-brood experiments indicate that this seasonal variation in thermal tolerance, along with seasonal variation in body size and phenotypic plasticity, is likely affected by genetic polymorphism. Our results show that adaptation to seasonal variation is important to consider when predicting how populations may respond to ongoing climate change.</p>
Limited plasticity in thermally tolerant ectotherm populations: evidence for a trade-off
<p></p><p>Many species face extinction risks owing to climate change, and there is an urgent need to identify which species' populations will be most vulnerable. Plasticity in heat tolerance, which includes acclimation or hardening, occurs when prior exposure to a warmer temperature changes an organism's upper thermal limit. The capacity for thermal acclimation could provide protection against warming, but prior work has found few generalizable patterns to explain variation in this trait. Here, we report the results of, to our knowledge, the first meta-analysis to examine within-species variation in thermal plasticity, using results from 20 studies (19 species) that quantified thermal acclimation capacities across 78 populations. We used meta-regression to evaluate two leading hypotheses. The climate variability hypothesis predicts that populations from more thermally variable habitats will have greater plasticity, while the trade-off hypothesis predicts that populations with the lowest heat tolerance will have the greatest plasticity. Our analysis indicates strong support for the trade-off hypothesis because populations with greater thermal tolerance had reduced plasticity. These results advance our understanding of variation in populations' susceptibility to climate change and imply that populations with the highest thermal tolerance may have limited phenotypic plasticity to adjust to ongoing climate warming.</p><p></p>
Rates of phenotypic plasticity in thermal tolerance
<p><span>An individual's fitness cost associated with environmental change likely depends on the rate of adaptive phenotypic plasticity, and yet our understanding of plasticity rates in an ecological and evolutionary context remains limited. We provide the first quantitative synthesis of existing plasticity rate data, focusing on acclimation of temperature tolerance in ectothermic animals, where we demonstrate applicability of a recently proposed analytical approach. The analyses reveal considerable variation in plasticity rates of this trait among species, with half-times (how long it takes for the initial deviation from the acclimated phenotype to be reduced by 50% when individuals are shifted to a new environment) ranging from 3.7 to 770.2 h. Furthermore, rates differ among higher taxa, being higher for amphibians and reptiles than for crustaceans and fishes, and with insects being intermediate. We argue that a more comprehensive understanding of phenotypic plasticity will be attained through increased focus on the rate parameter.</span></p>
Thermal plasticity of the sea urchin Salmacis sphaeroides
<p>Data of metabolic rates of sea urchin acclimated to two different temperatures.</p>
Data from: Does local adaptation along a latitudinal cline shape plastic responses to combined thermal and nutritional stress?
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Data from: Evolution of cold tolerance and thermal plasticity in life history, behaviour and physiology during a poleward range expansion
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Interindividual plasticity in metabolic and thermal tolerance traits from populations subjected to recent anthropogenic heating
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Data from: Plasticity of thermal tolerance and its relationship with growth rate in juvenile mussels (Mytilus californianus)
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Data from: Variation in the thermal plasticity of avian embryos is produced by the developmental environment, not genes
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Data from: Adaptive thermal plasticity enhances sperm and egg performance in a model insect
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Genetic differentiation underlies seasonal variation in thermal tolerance, body size, and plasticity in a short-lived copepod
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