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231 results for “adaptive plasticity”
Data from: Tradeoffs affect the adaptive value of plasticity: Stronger cannibal-induced defenses incur greater costs in toad larvae
<p>Adaptive developmental plasticity allows individuals to match their phenotype with their environment, which can increase fitness where threats are inconsistently present. Because adaptive traits are not ubiquitously nor infinitely plastic, tradeoffs between benefits and costs or limits are theoretically necessary to constrain plastic responses. Systems in which extreme risk can be reliably detected are ideal for investigating mechanisms that constrain plasticity, as even costly responses may be adaptive where risk is severe. Cane toads (<em>Rhinella marina</em>) are abundant in Australia and produce large clutches (frequently >10,000 eggs), but asynchronous breeding and rapid development result in variable larval densities within breeding pools. In the field, we found that cannibalism by older cohorts often reduces the survival of conspecific eggs and newly hatched pre-feeding larvae ("hatchlings") by >99%, as feeding larvae ("tadpoles") use chemical cues from the relatively immobile hatchlings to locate and consume them. After hatchlings become free-swimming, however, they are safe from cannibalism. Hatchlings can reduce this period of vulnerability by accelerating development when they detect conspecific tadpole cues. However, this developmental acceleration decreases initial tadpole mass, reduces subsequent survival, growth, and development, affects behavior, and compromises feeding structures. Reaction norms differ among clutches, and greater developmental acceleration is followed by greater impairment of larval function in plastic clutches, whereas nonresponsive clutches are unaffected by exposure to cannibal cues. More plastic clutches ultimately exhibit both poorer performance and greater variation among siblings in exposed and (to a lesser degree) control treatments. Variation among clutches in tadpole viability is driven by differences in plasticity rather than phenotype; fitness reductions are linked to developmental acceleration, not rapid development <em>per se</em>. Clutches with intrinsically slow pre-feeding developmental rates exhibit stronger acceleration (i.e., steeper reaction norms), but clutches with intrinsically rapid development reach invulnerable stages more quickly than those that accelerate development. As a result, high cannibalism risk may favor canalized rapid development rather than facultative developmental acceleration. Cannibalism plays an important role in the recruitment of this invasive species, and hatchling defenses against this threat demonstrate how the limits and tradeoffs associated with an inducible defense can favor canalized defenses over phenotypic plasticity.</p>
Data from: Plasticity versus evolutionary divergence: what causes habitat partitioning in urban-adapted birds?
<p>Habitat partitioning can facilitate the coexistence of closely related species, and often results from competitive interference inducing plastic shifts of subordinate species in response to aggressive, dominant species (plasticity), or the evolution of ecological differences in subordinate species that reduce their ability to occupy habitats where the dominant species occurs (evolutionary divergence). Evidence consistent with both plasticity and evolutionary divergence exist, but the relative contributions of each to habitat partitioning have been difficult to discern. Here we use a global dataset on the breeding occurrence of birds in cities to test predictions of these alternative hypotheses to explain previously described habitat partitioning associated with competitive interference. Consistent with plasticity, the presence of behaviorally dominant congeners in a city was associated with a 65% reduction in occurrence of subordinate species, but only when the dominant was a widespread breeder in urban habitats. Consistent with evolutionary divergence, increased range-wide overlap with dominant congeners was associated with a 56% reduction in occurrence of subordinates in cities, even when the dominant was absent from the city. Overall, our results suggest that both plasticity and evolutionary divergence play important, concurrent roles in habitat partitioning among closely related species in urban environments.</p>
Data from: Local adaptation for enhanced salt tolerance reduces non-adaptive plasticity caused by osmotic stress
Organisms often respond to environmental change via phenotypic plasticity, where an individual modulates its phenotype according to the environment. Highly variable or changing environments can exceed physiological limits and generate maladapted plastic phenotypes, which is termed non-adaptive plasticity. In some cases, selection may reduce the negative or disruptive impacts of environmental stress and produce locally adapted populations. Salt is an increasingly prevalent contaminant of freshwater systems and can induce non-adaptive plastic phenotypes for freshwater organisms like amphibians. Hyla cinerea is a frog species with populations inhabiting brackish, coastal habitats, so we use this species to test whether coastal populations are locally adapted to tolerate saltwater by determining how salt exposure during the embryonic and larval stages alters mortality and plastic developmental and metamorphic phenotypes of coastal and inland populations. Coastal frogs have higher survival, faster growth rates, and metamorphose sooner than inland frogs across salinities. Coastal frogs also metamorphose smaller (likely a consequence of earlier metamorphosis) yet maintain constant size, while higher salinities reduce metamorphic size for inland frogs. Coastal frogs evolved to minimize non-adaptive and disruptive impacts of saltwater during larval development and accelerate the larval period to reduce time spent in a stressful environment.
Sexual selection buffers the negative consequences of population fragmentation on adaptive plastic responses to increasing temperatures
<p class="MsoNormal"><span>Whether sexual selection facilitates or hampers the ability to plastically respond to novel environments might depend on population structure, via its effects on </span><span>sexual interactions and associated fitness payoffs</span><span>. Using experimentally evolved lines </span><span>of the seed beetle <em>Callosobruchus maculatus,</em> we tested whether individuals evolving under different sexual selection (monogamy vs polygamy) and population spatial structure (metapopulation vs undivided populations) treatments differed in their response across developmental thermal conditions (control, hot or stressful) in a range of fitness and fitness-associated traits. We found that individuals from subdivided populations had lower lifetime reproductive success (LRS) at hot temperatures, but only in lines evolving under relaxed sexual selection, revealing a complex interaction between sexual selection, population structure, and thermal environmental stress on fitness. We also found an effect of population structure on several traits, including fertility and adult emergence success, under exposure to high thermal conditions. Finally, we found a strong negative effect of hot and stressful temperatures in fitness and associated traits. Our results show that population structure can exacerbate the impact of a warming climate, potentially leading to declines in population viability, but that sexual selection can buffer the negative influence of population subdivision on adaptation to warm temperatures</span><span>.</span></p>
Data from: Adaptive responses and transgenerational plasticity of a submerged plant to benthivorous fish disturbance
<p>Benthivorous fish dominance in some subtropical lakes may alter submerged plant growth, reproduction, and progeny germination by changing water-submerged plant-algae interactions. We conducted mesocosm experiments to examine the effects of three densities of benthivorous fish, <em>Misgurnus anguillicaudatus</em>, on the water properties, the growth, asexual reproduction, and the germination of turions of <em>Potamogeton crispus</em> L.</p> <p>The dataset includes water environment characteristics, macrophyte traits, algae traits, and sediment nutrient characteristics. Macrophyte traits include morphological, stoichiometric, turion traits, and germination traits.</p>
Physiological and environmental data from: Are you ready for the heat? Plasticity vs adaptation of heat tolerance in three-spined stickleback
<p>Heat waves constitute a challenge for aquatic ectotherms. However, the thermal tolerance of animals and their individual phenotypic plasticity to respond to heat waves may be influenced by thermal history. We tested these hypotheses by comparing the upper thermal tolerance and the individual capacities of three-spined sticklebacks from populations with different thermal histories to respond to heat waves. Two populations originated from thermally polluted nuclear power plant (NPP) habitats, while four locations represented geographically adjacent control areas. To disentangle the genetic adaptation from the phenotypic plastic response, we measured the individual upper thermal tolerance and the responses at molecular level in common garden conditions before and after a laboratory-mimicked heat wave. We found that the sticklebacks exhibit considerable phenotypic plasticity in thermal tolerance since the heat wave increased fish upper thermal tolerance significantly. The individual plasticity to respond to the heat wave was also negatively correlated to initial thermal tolerance. On the other hand, neither the thermal tolerance nor the plastic responses differed between NPP and control sites despite detection of significant but low genome-wide divergence in 10 out of 15 pairwise comparisons. Our results suggest that five decades of nuclear power plant activity with warmer water has not resulted in a detectable evolutionary change in either the upper thermal tolerance or its plasticity in three-spined sticklebacks potentially rendering them sensitive to frequent heat waves.</p>
Adaptive and non-adaptive plasticity in changing environments: implications for sexual species with different life history strategies
<p>Populations adapt to novel environmental conditions by genetic changes or phenotypic plasticity. Plastic responses are generally faster and can buffer fitness losses under variable conditions. Plasticity is typically modelled as random noise and linear reaction norms that assume simple one-to-one genotype-phenotype maps and no limits to the phenotypic response. Most studies on plasticity have focused on its effect on population viability. However, it is not clear, whether the advantage of plasticity depends solely on environmental fluctuations or also on the genetic and demographic properties (life histories) of populations. Here we present an individual-based model and study the relative importance of adaptive and non-adaptive plasticity for populations of sexual species with different life histories experiencing directional stochastic climate change. Environmental fluctuations were simulated using differentially autocorrelated climatic stochasticity or noise color, and scenarios of directional climate change. Non-adaptive plasticity was simulated as a random environmental effect on trait development, while adaptive plasticity as a linear, saturating, or sinusoidal reaction norm. The last two imposed limits to the plastic response and emphasized flexible interactions of the genotype with the environment. Interestingly, this assumption led to (i) smaller phenotypic than genotypic variance in the population (many-to-one genotype-phenotype map) and the coexistence of polymorphisms, and (ii) the maintenance of higher genetic variation – compared to linear reaction norms and genetic determinism – even when the population was exposed to a constant environment for several generations. Limits to plasticity led to genetic accommodation, when costs were negligible, and to the appearance of cryptic variation when limits were exceeded. We found that adaptive plasticity promoted population persistence under red environmental noise and was particularly important for life histories with low fecundity. Populations producing more offspring could cope with environmental fluctuations solely by genetic changes or random plasticity, unless environmental change was too fast.</p>
Adaptive divergence generates distinct plastic responses in two closely related Senecio species
<p><span>The evolution of plastic responses to external cues allows species to maintain fitness in response to the environmental variation they regularly experience. However, it remains unclear how plasticity evolves during adaptation. To test whether distinct patterns of plasticity are associated with adaptive divergence, we quantified plasticity for two closely related but ecologically divergent Sicilian daisy species (<i>Senecio, </i>Asteraceae). We sampled c.40 representative genotypes of each species from their native range on Mt Etna and then reciprocally transplanted multiple clones of each genotype into four field sites along an elevational gradient that included the native elevational range of each species, and two intermediate elevations. At each elevation we quantified survival and measured leaf traits that included investment (specific leaf area), morphology, chlorophyll fluorescence, pigment content and gene expression. Traits and differentially expressed genes that changed with elevation in one species often showed little change in the other species, or changed in the opposite direction. As evidence of adaptive divergence, both species performed better at their native site and better than the species from the other habitat. Adaptive divergence is therefore associated with the evolution of distinct plastic responses to environmental variation, despite these two species sharing a recent common ancestor.</span></p>
Stay in shape: assessing the adaptive potential of shell morphology and its sensitivity to temperature in the invasive New Zealand Mud Snail Potamopyrgus antipodarum through phenotypic plasticity and natural selection in Europe
<p>Climate change may force organisms to adapt genetically or plastically to new environmental conditions. Invasive species show a remarkable potential for rapid adaptation. The ovoviviparous New Zealand mud snail (NZMS), <em>Potamopyrgus antipodarum</em>, has successfully established across Europe with two clonally reproducing mitochondrial lineages since its arrival in the first half of the 19th century. Its remarkable variation in shell morphology was shown to be fitness relevant. We investigated the effects of temperature on shell morphology across eleven populations from Germany and the Iberian Peninsula in a common garden across three temperatures. We analysed size and shape using geometric morphometrics. For both, we compared reaction norms and estimated heritabilities. For size, the interaction of temperature and haplotype explained about 50% of the total variance. We also observed more genotype by environment interactions indicating a higher degree of population differentiation than in shape. Across the three temperatures, size followed the expectations of the temperature-size rule, with individuals growing larger in cold environments. Changes in shape may have compensated changes in size affecting space for brooding embryos. Heritability estimates were relatively high. As indicated by the very low coefficients of variation for clonal repeatability (<em>CV<sub>A</sub></em>), they can probably not be compared in absolute terms. However, they showed some sensitivity to temperature, in haplotype t more so than in z, which was only found in Portugal. The low <em>CV<sub>A</sub></em>-values indicate that genetic variation among European populations is still restricted with low potential to react to selection. A considerable fraction of the genetic variation was due to differences between the clonal lineages. The NZMS has apparently not been long enough in Europe to accumulate significant genetic variation relevant for morphological adaptation. As temperature is obviously not the sole factor influencing shell morphology, their interaction will probably not be a factor limiting population persistence under a warming climate in Europe.</p>
Community-wide trait adaptation, but not plasticity, explain ant community structure in extreme environments
<p>1. Quantifying trait-environment associations can help elucidate the processes underpinning the structure of species assemblages. However, most work has focused on trait variation across rather than within species, meaning that processes operating at the intraspecific levels cannot be detected. Incorporating intraspecific trait variation in community-wide analyses can provide valuable insights about the role of morphological adaptation and plasticity on species persistence and the composition of ecological communities.</p> <p>2. Here, we assessed geographic variation in the direction (i.e., adaptation) and strength of selection, and the magnitude of plasticity, by examining community-wide trait variation in ant communities along an environmental gradient spanning 9° latitude in Quebec, Canada. Specifically, we measured 9 morphological traits related to foraging strategies, resource use and thermal regulation at 20 locations across temperate and boreal forests. We then examined how the mean and variance of these traits varied along temperature and precipitation gradients. Moreover, we examined how these trait-environment relationships varied across levels of organization, from individual workers (intraspecific) to colonies (intraspecific) and species (interspecific).</p> <p>3. We observed changes in mean trait values along environmental gradients, but very little change in variance. Specifically, we observed a decrease in the mean length of antennae and an increase in the mean eye length from mild (warm and wet) to more extreme environments (cold and dry). These shifts in trait means were mostly coordinated across organizational levels (i.e., worker, colony, and species). We also observed a general increase in trait variance from mild to extreme environments, but only at the species level.</p> <p>4. Our findings suggest that stressful environmental conditions exert a strong selection pressure on ant morphology causing shifts in optimal trait values. These adaptations may enable persistence at the northern edge of the boreal forest and therefore influence the composition of these ant communities. Specifically, ants with large eyes and short antennae are overrepresented at the transition zone between the boreal forest and the tundra, possibly representing an adaptation to these more open habitats. Our study demonstrates that combining spatial and community-wide intraspecific functional trait data provides a promising way forward to gain new insights on trait adaptations and processes underpinning community structure along environmental gradients.</p>
Urbanization extends flight phenology and leads to local adaptation of seasonal plasticity in Lepidoptera
<p>Urbanization is globally gaining force and challenges biodiversity but has recently also emerged as an agent of evolutionary change. Seasonal phenology and life-cycle regulation are essential processes that urbanization is likely to alter through both the urban-heat-island effect (UHI) and artificial-light-at-night (ALAN). However, how UHI and ALAN affect the evolution of seasonal adaptations has received little attention. Here, we test for urban evolution of seasonal life-history plasticity, specifically changes in the photoperiodic induction of diapause in two lepidopterans, <i>Pieris napi </i>(Pieridae) and <i>Chiasmia clathrata</i> (Geometridae). We used long-term data from standardized monitoring and citizen science observation schemes to compare yearly phenological flight curves in six cities in Finland and Sweden to those of adjacent rural populations. This analysis showed for both species that flight seasons are longer and end later in most cities, suggesting a difference in timing of diapause induction. Then, we used common-garden experiments to test whether evolution of the photoperiodic reaction norm for diapause could explain these phenological changes for a subset of these cities. These experiments demonstrated a genetic shift for both species in urban areas towards a lower daylength threshold for direct development, consistent with predictions based on the UHI but not ALAN. The correspondence of this genetic change to the results of our larger-scale observational analysis of <i>in situ</i> flight phenology indicates that it may be widespread. These findings suggest that seasonal life-cycle regulation evolves in urban ectotherms and may contribute to eco-evolutionary dynamics in cities.</p>
Within-generation and transgenerational social plasticity interact during rapid adaptive evolution
<p>The effects of within-generation plasticity versus transgenerational plasticity on trait expression are poorly understood, but important for evaluating plasticity's evolutionary consequences. We tested how genetics, within-generation plasticity, and transgenerational plasticity jointly shape traits influencing rapid evolution in the field cricket <em>Teleogryllus oceanicus</em>. In Hawaiian populations attacked by acoustically-orienting parasitoid flies, a protective, X-linked variant ("<em>flatwing</em>") eliminates male acoustic sexual signals. Silent males rapidly spread to fixation, dramatically changing the acoustic environment. First, we found evidence supporting <em>flatwing</em>-associated pleiotropy in juveniles: pure-breeding <em>flatwing</em> males and females exhibit greater locomotion than those with <em>normal-wing</em> genotypes. Second, within-generation plasticity caused homozygous-<em>flatwing</em> females developing in silence, which mimics all-<em>flatwing</em> populations, to attain lower adult body condition and reproductive investment than those experimentally exposed to song. Third, maternal song exposure caused transgenerational plasticity in offspring, affecting adult, but not juvenile, size, condition, and reproductive investment. This contrasted with behavioral traits, which were only influenced by within-generation plasticity. Fourth, we matched and mismatched maternal and offspring social environments and found that transgenerational plasticity sometimes interacted with within-generation plasticity and sometimes opposed it. Our findings stress the importance of evaluating the plasticity of different traits and stages across generations when evaluating their fitness consequences and role in adaptation.</p>
Data for: Adaptive plasticity to drought of Grime's CSR strategies
<p>Grime's strategies (Competitor, Stress tolerator, Ruderal; CSR) represent viable trait combinations with which species deal with environmental conditions. CSR strategies are broadly used to understand plant adaptation to the environment, yet their plastic responses have received little attention. A globally-calibrated tool (StrateFy) estimates CSR strategies using specific leaf area (SLA), leaf dry matter content (LDMC) and leaf area (LA) data, but these three traits can hardly characterise whole-plant responses to the environment individually. CSR strategies reflect trade-offs among growth, survival and reproduction, at both leaf and whole-plant levels, thus integrating several functions. We hypothesised that CSR strategies and the three constituent traits would show independent plasticity patterns, and that CSR strategies would be more likely to show adaptive responses, i.e., to fit expected functional responses to environmental gradients. We compared phenotypic plasticity to drought in single traits (SLA, LDMC and LA) with the integrated plasticity of the resulting CSR strategy. The study species was the invasive plant <em>Mesembryanthemum crystallinum</em>, which is distributed in arid and semiarid Chile. We found that trait plasticity was rather idiosyncratic and contrary to what would be expected from a functional adjustment to drought: LDMC did not change (expected response: increase) and SLA increased (expected response: decrease). Conversely, plastic responses of CSR strategy and LA were consistent with functionally adaptive responses to drought in all populations: S-strategy increased, while C-strategy and LA decreased. We advocate the use of Grime's CSR theory as an integrative approach to further our understanding of adaptive plasticity in plants.</p>
Fig. 8 in Sex-ratio and body size plasticity in two cold-adapted ground beetles co-occurring in a periglacial area of the European Alps (Coleoptera: Carabidae)
Fig. 8 – Linear regression graph between elytra width of Nebria castanea females and the soil pH.
Fig. 1 in Sex-ratio and body size plasticity in two cold-adapted ground beetles co-occurring in a periglacial area of the European Alps (Coleoptera: Carabidae)
Fig. 1 – Sampling plan: distribution of pitfall traps at the Lazaunkar site.
Data from: Does local adaptation along a latitudinal cline shape plastic responses to combined thermal and nutritional stress?
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Within-generation and transgenerational social plasticity interact during rapid adaptive evolution
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Data from: Gene expression plasticity as a mechanism of coral adaptation to a variable environment
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Data from: Tradeoffs affect the adaptive value of plasticity: Stronger cannibal-induced defenses incur greater costs in toad larvae
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Pre-adaptation to climate change through topography-driven evolution of traits and their plasticity
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