Rapid Evolutionary Response Research Articles

Rapid evolution as a possible constraint on emerging infectious diseases

Summary1. Emerging infectious diseases may decimate populations or become endemic, but such worst‐case scenarios do not occur as frequently as might be expected, even for virulent parasites.2. One explanation for this apparent paradox is that rapid evolution of host resistance may diminish or terminate epidemics. Theoretical and empirical studies have shown that evolution in host–parasite systems can dramatically alter the prevalence and intensity of infection.3. The potential for rapid evolution to protect host populations from negative effects of virulent parasites depends on the type of parasite‐driven evolution that occurs. In some host–parasite systems, evolution of increased host resistance can terminate epidemics. However, evolution resulting from parasite‐mediated disruptive selection might actually allow a disease to persist in the host population. Epidemics may also be sustained through coevolution of the parasite.4. The rate of evolution and subsequent disease dynamics will be affected by both the diversity of the host population and the community context in which the host–parasite interaction is embedded. Predators, competitors and food resources can all affect the rates of evolution of hosts and parasites and interact with evolution to determine the outcome of epidemics.5. Freshwater organisms have played an important role in the studies of eco‐evolutionary dynamics. Rapid evolution in response to parasitism has been demonstrated in multiple freshwater host species, which appears to have protected some of these populations from the virulent effects of infectious diseases.6. Studies of emerging infectious diseases in freshwater ecosystems should consider the possibility of evolution of hosts and/or parasites on ecological timescales, since this phenomenon can profoundly affect disease dynamics.

Female mate preferences inDrosophila simulans: evolution and costs

Female mate preference is central to sexual selection, and all indirect benefit models require that there is genetic variation in female preference. This has rarely been tested however, with relatively few studies documenting heritable variation in female preference and even fewer that have directly selected on mate preference to unequivocally show that it can evolve. Additionally, costs of mate preference are poorly understood even though these have implications for preference evolution. We selected on female preference for ebony-males in replicate Drosophila simulans lines, and generated a rapid evolutionary response in both replicates, with the proportion of females mating with ebony-males increasing from approximately 5% to 30% after five generations of selection. This increase was independent of changes in ebony-males as only females were included in our selection regime. We could detect no cost to mate preference itself other than that associated with the fitness consequences of mating with ebony males.

Quantitative Genetics of Pigmentation Development in 2 Populations of the Common Garter Snake, Thamnophis sirtalis

The evolutionary importance of ontogenetic change has been noted since Darwin. However, most analyses of phenotypic evolution focus on single landmark ages. Here, we present an inheritance study that quantifies genetic variation in pigmentation across early-age (i.e., birth to 180 days) development in 2 populations of the common garter snake, Thamnophis sirtalis. The populations are phenotypically distinct and geographically isolated (Manitoba, CA and Northern California, USA). There were highly significant differences between populations for the developmental trajectory of mean pigmentation, with the Manitoba population exhibiting a mean pigmentation level that increased across ontogeny, whereas the California population exhibited mean pigmentation that was invariant across ontogeny. Subsequent quantitative genetic analyses revealed heritable variation at all ages in Manitoba but low levels of phenotypic and genetic variation in California at all ages. A quantitative genetic decomposition of the longitudinal genetic variance-covariance matrix for the age-specific pigmentation phenotypes in the Manitoba population revealed 2 primary orthogonal axes that explained most ( approximately 100%) of the pigmentation variation across ontogeny. The primary axis, explaining 93% of the genetic variation, is an axis of genetic variation whose principal value loadings change from positive to negative across development, suggesting that the most rapid evolutionary response to selection on pigmentation variation will occur in the direction characterized by a tradeoff in early-age versus late-age pigmentation phenotypes. Pigmentation is known to be ecologically important and subject to rapid evolution under selection. Our study shows that significant differences exist between these 2 populations for their capacity to respond to selection on pigmentation which is not only influenced by the population of origin but also by the developmental process. We suggest that developmental timing may be a potential explanatory mechanism for the difference between the populations.

Is there rapid evolutionary response in introduced populations of tansy ragwort, Jacobaea vulgaris, when exposed to biological control?

Differences in the herbivore community between a plant’s native (specialists and generalists) and introduced range (almost exclusively generalists) may lead to the evolution of reduced allocation to defences against specialist herbivores in the introduced range, allowing for increased allocation to competitive ability and to defences against generalist herbivores. Following this logic, the introduction of biological control agents should reverse this evolutionary shift and select for plants with life-history traits that are more similar to those of plants in the native range than those of plants in the introduced range that have not been exposed to biological control. In a common garden experiment, we compared performance and resistance traits of tansy ragwort, Jacobaea vulgaris, among populations from the introduced range (New Zealand and North America) that have either been exposed to or grown free from the biological control agent Longitarsus jacobaeae. For comparison, we included populations from the native European range. We found lower levels of generalist-deterrent pyrrolizidine alkaloids (PAs) and of soluble phenolics in New Zealand populations with than in populations without exposure to L. jacobaeae, while the opposite pattern was detected among North American populations. Contrary to expectation, populations with exposure to L. jacobaeae revealed more feeding damage by L. jacobaeae than populations without exposure. Introduced populations had higher levels of PAs and reproductive output than native J. vulgaris populations. Jacobaea vulgaris was introduced in different parts of the world some 100–130 years ago, while L. jacobaeae was introduced only some 20–40 years ago. Hence, the larger differences observed between native and introduced populations, as compared to introduced populations with and without biological control history, may result from different time scales available for selection to act.

Possible contemporary evolution in an endangered species, the Santa Cruz Island fox

AbstractAn ability to mount rapid evolutionary responses to environmental change may be necessary for species persistence in a human‐dominated world. We present evidence of the possibility of such contemporary evolution in the anti‐predator behaviour of the critically endangered Santa Cruz Island fox Urocyon littoralis. In 1994, golden eagles colonized Santa Cruz Island, CA and devastated the predator‐naïve, endemic island fox population by 95% within 10 years. In 1992, just before the arrival of golden eagles, foxes showed substantial diurnal activity, but diurnal activity was 37.0% lower in 2003–2007, after golden eagle colonization; concurrently, overall activity declined and nocturnal activity increased. Moreover, on nearby Santa Catalina Island, where golden eagles were absent but where the fox population recently crashed due to a disease epidemic, remaining foxes were significantly more diurnally active than were those on Santa Cruz Island. The weight of evidence suggests that the change in activity pattern was a response to predation, not to low population density, and that this was probably a heritable rather than a learned behavioural trait. This behavioural change may allow for prolonged island fox persistence, but also potentially represents a loss of behavioural diversity in fox populations.

POPULATION DYNAMICS DETERMINE GENETIC ADAPTATION TO TEMPERATURE INDAPHNIA

Rising temperatures associated with global warming present a challenge to the fate of many aquatic organisms. Although rapid evolutionary response to temperature-mediated selection may allow local persistence of populations under global warming, and therefore is a key aspect of evolutionary biology, solid proof of its occurrence is rare. In this study, we tested for genetic adaptation to an increase in temperature in the water flea Daphnia magna, a keystone species in freshwater systems, by performing a thermal selection experiment under laboratory conditions followed by the quantification of microevolutionary responses to temperature for both life-history traits as well as for intraspecific competitive strength. After three months of selection, we found a microevolutionary response to temperature in performance, but only in one of two culling regimes, highlighting the importance of population dynamics in driving microevolutionary change within populations. Furthermore, there was an evolutionary increase in thermal plasticity in performance. The results of the competition experiment were in agreement with predictions based on performance as quantified in the life table experiment and illustrate that microevolution within a short time frame has the ability to influence the outcome of intraspecific competition.

Simulated climate change provokes rapid genetic change in the Mediterranean shrub Fumana thymifolia

AbstractRapid climate change will impose strong directional selection pressures on natural plant populations. Climate‐linked genetic variation in natural populations indicates that an evolutionary response is possible. We investigated such a response by comparing individuals subjected to elevated drought and warming treatments with individuals establishing in an unmanipulated climate within the same population. We report that reduction in seedling establishment in response to climate manipulations is nonrandom and results from the selection pressure imposed by artificially warmed and droughted conditions. When compared against control samples, high single‐locus genetic divergence occurred in drought and warming treatment samples, with genetic differentiation up to 37 times higher than background (mean neutral locus) genetic differentiation. These loci violate assumptions of selective neutrality, indicating the signature of natural selection by drought. Our results demonstrate that rapid evolution in response to climate change may be widespread in natural populations, based on genetic variation already present within the population.

Do hormonal control systems produce evolutionary inertia?

Hormonal control systems are complex in design and well integrated. Concern has been raised that these systems might act as evolutionary constraints when animals are subject to anthropogenic environmental change. Three systems are examined in vertebrates, especially birds, that are important for assessing this possibility: (i) the hypothalamic-pituitary-gonadal (HPG) axis, (ii) the activational effects of sex steroids on mating effort behaviour, and (iii) sexual differentiation. Consideration of how these systems actually work that takes adequate account of the brain's role and mechanisms suggests that the first two are unlikely to be impediments to evolution. The neural and molecular networks that regulate the HPG provide both phenotypic and evolutionary flexibility, and rapid evolutionary responses to selection have been documented in several species. The neuroendocrine and molecular cascades for behaviour provide many avenues for evolutionary change without requiring a change in peripheral hormone levels. Sexual differentiation has some potential to be a source of evolutionary inertia in birds and could contribute to the lack of diversity in certain reproductive (including life history) traits. It is unclear, however, whether that lack of diversity would impede adaptation to rapid environmental change given the role of behavioural flexibility in avian reproduction.

Evolution in ecological field experiments: implications for effect size

Rapid evolution in response to strong selection, much of which is human-induced, has been indisputably documented. In this perspective, we suggest that adaptation may influence the effect size of treatments in ecological field experiments and alter our predictions of future dynamics in ecological systems. Field experiments often impose very strong and consistent selection over multiple generations. Focal populations may adapt to these treatments and, in the process, increase or decrease the magnitude of the treatment effect through time. We argue that how effect size changes through time will depend on the evolutionary history of the experimental population, the type of experimental manipulation, and the traits involved in adaptive responses. While no field study has conclusively demonstrated evolution in response to treatments with concomitant changes in ecological effect size, we present several examples that provide strong circumstantial evidence that such effects occur. We conclude with a consideration of the differences between plastic and genetic responses to treatments and discuss future research directions linking adaptation to ecological effect size.

The genetic basis of traits regulating sperm competition and polyandry: can selection favour the evolution of good- and sexy-sperm?

The good-sperm and sexy-sperm (GS-SS) hypotheses predict that female multiple mating (polyandry) can fuel sexual selection for heritable male traits that promote success in sperm competition. A major prediction generated by these models, therefore, is that polyandry will benefit females indirectly via their sons' enhanced fertilization success. Furthermore, like classic 'good genes' and 'sexy son' models for the evolution of female preferences, GS-SS processes predict a genetic correlation between genes for female mating frequency (analogous to the female preference) and those for traits influencing fertilization success (the sexually selected traits). We examine the premise for these predictions by exploring the genetic basis of traits thought to influence fertilization success and female mating frequency. We also highlight recent debates that stress the possible genetic constraints to evolution of traits influencing fertilization success via GS-SS processes, including sex-linked inheritance, nonadditive effects, interacting parental genotypes, and trade-offs between integrated ejaculate components. Despite these possible constraints, the available data suggest that male traits involved in sperm competition typically exhibit substantial additive genetic variance and rapid evolutionary responses to selection. Nevertheless, the limited data on the genetic variation in female mating frequency implicate strong genetic maternal effects, including X-linkage, which is inconsistent with GS-SS processes. Although the relative paucity of studies on the genetic basis of polyandry does not allow us to draw firm conclusions about the evolutionary origins of this trait, the emerging pattern of sex linkage in genes for polyandry is more consistent with an evolutionary history of antagonistic selection over mating frequency. We advocate further development of GS-SS theory to take account of the complex evolutionary dynamics imposed by sexual conflict over mating frequency.

Rapid evolution in response to introduced predators II: the contribution of adaptive plasticity

BackgroundIntroductions of non-native species can significantly alter the selective environment for populations of native species, which can respond through phenotypic plasticity or genetic adaptation. We examined phenotypic and genetic responses of Daphnia populations to recent introductions of non-native fish to assess the relative roles of phenotypic plasticity versus genetic change in causing the observed patterns. The Daphnia community in alpine lakes throughout the Sierra Nevada of California (USA) is ideally suited for investigation of rapid adaptive evolution because there are multiple lakes with and without introduced fish predators. We conducted common-garden experiments involving presence or absence of chemical cues produced by fish and measured morphological and life-history traits in Daphnia melanica populations collected from lakes with contrasting fish stocking histories. The experiment allowed us to assess the degree of population differentiation due to fish predation and examine the contribution of adaptive plasticity in the response to predator introduction.ResultsOur results show reductions in egg number and body size of D. melanica in response to introduced fish. These phenotypic changes have a genetic basis but are partly due to a direct response to chemical cues from fish via adaptive phenotypic plasticity. Body size showed the largest phenotypic change, on the order of nine phenotypic standard deviations, with approximately 11% of the change explained by adaptive plasticity. Both evolutionary and plastic changes in body size and egg number occurred but no changes in the timing of reproduction were observed.ConclusionNative Daphnia populations exposed to chemical cues produced by salmonid fish predators display adaptive plasticity for body size and fecundity. The magnitude of adaptive plasticity was insufficient to explain the total phenotypic change, so the realized change in phenotypic means in populations exposed to introduced fish may be the result of a combination of initial plasticity and subsequent genetic adaptation. Our results suggest that immediately following the introduction of fish predators, adaptive plasticity may reduce the impact of selection through "Baldwin/Bogert effects" by facilitating the movement of populations toward new fitness optima. Our study of the response of a native species to an introduced predator enhances our understanding of the conditions necessary for rapid adaptive evolution and the relationship between rapid evolution and adaptive phenotypic plasticity.

Rapid evolution in response to introduced predators I: rates and patterns of morphological and life-history trait divergence.

BackgroundIntroduced species can have profound effects on native species, communities, and ecosystems, and have caused extinctions or declines in native species globally. We examined the evolutionary response of native zooplankton populations to the introduction of non-native salmonids in alpine lakes in the Sierra Nevada of California, USA. We compared morphological and life-history traits in populations of Daphnia with a known history of introduced salmonids and populations that have no history of salmonid introductions.ResultsOur results show that Daphnia populations co-existing with fish have undergone rapid adaptive reductions in body size and in the timing of reproduction. Size-related traits decreased by up to 13 percent in response to introduced fish. Rates of evolutionary change are as high as 4,238 darwins (0.036 haldanes).ConclusionSpecies introductions into aquatic habitats can dramatically alter the selective environment of native species leading to a rapid evolutionary response. Knowledge of the rates and limits of adaptation is an important component of understanding the long-term effects of alterations in the species composition of communities. We discuss the evolutionary consequences of species introductions and compare the rate of evolution observed in the Sierra Nevada Daphnia to published estimates of evolutionary change in ecological timescales.

Rapid evolutionary responses in a translocated population of intertidal snail (Bembicium vittatum) utilise variation from different source populations

The artificial movement of individuals between populations (translocation) can be an effective way to increase genetic diversity within populations, but few studies have undertaken long term genetic monitoring to determine if variation introduced by translocation is maintained over many generations or whether it can be used to adapt to local conditions. Here, we report on the changes in morphological and molecular variation over a 12-year period in a population of an intertidal littorine snail (Bembicium vittatum) that was created by mixing individuals from three geographically disjunct populations. These source populations differ genetically in shell shape and in allele frequency at several allozyme loci. We found that the translocated population had higher allozyme diversity than any of the source populations and that this pattern was maintained over multiple generations. Variation in shell shape also increased, but this declined over time as shells became taller. Some allozyme loci also showed significant changes in frequency over time. These changes were not consistently towards the genetic makeup of a single source population, and in the case of shell shape, were towards a phenotype that was most suited to the local environment. Our results suggest that genetic variation introduced into a population by translocation can be rapidly incorporated and used to adapt to local conditions without domination by a single source population’s genome. However, more studies are needed before generalisations on the benefits of mixing individuals from disjunct populations can be made.

Analysis of Homologous Gene Clusters inCaenorhabditis elegansReveals Striking Regional Cluster Domains

An algorithm for detecting local clusters of homologous genes was applied to the genome of Caenorhabditis elegans. Clusters of two or more homologous genes are abundant, totaling 1391 clusters containing 4607 genes, over one-fifth of all genes in C. elegans. Cluster genes are distributed unevenly in the genome, with the large majority located on autosomal chromosome arms, regions characterized by higher genetic recombination and more repeat sequences than autosomal centers and the X chromosome. Cluster genes are transcribed at much lower levels than average and very few have gross phenotypes as assayed by RNAi-mediated reduction of function. The molecular identity of cluster genes is unusual, with a preponderance of nematode-specific gene families that encode putative secreted and transmembrane proteins, and enrichment for genes implicated in xenobiotic detoxification and innate immunity. Gene clustering in Drosophila melanogaster is also substantial and the molecular identity of clustered genes follows a similar pattern. I hypothesize that autosomal chromosome arms in C. elegans undergo frequent local gene duplication and that these duplications support gene diversification and rapid evolution in response to environmental challenges. Although specific gene clusters have been documented in C. elegans, their abundance, genomic distribution, and unusual molecular identities were previously unrecognized.

Rapid Evolutionary Responses to Selection in Heterogeneous Environments among Agricultural and Nonagricultural Weeds

Agricultural settings are hypothesized to impose strong selection on invading weed species, and the direction of selection can be consistent across many generations, depending on crop‐rotation schedules. Because the history of selection is often known, agricultural environments provide a useful experimental setting for studies testing mechanisms of adaptation and rates of evolutionary response. Here, two populations of Abutilon theophrasti with known evolutionary histories of competing either in agricultural or nonagricultural settings were reciprocally transplanted across experimental treatments simulating the site of origin (rotating corn and soybean cultivation, local weeds, or no‐competition control). Consistent with hypotheses of local adaptation, the agricultural population had higher fitness than the nonagricultural population in the cornfield treatment. The nonagricultural population had higher fitness in the no‐competition control. Because weedy, nonagricultural sites are typically patchy and consist of both high‐ and low‐density (i.e., noncompetitive) microsites, the observed population differences in fitness in the no‐competition control also indicate local adaptation. In addition to fitness, the two populations differed in the expression of life‐history traits such that the life‐history of the agricultural population was accelerated relative to the nonagricultural population. The observed life‐history differences probably reflect adaptive synchronization of life‐history events to the shorter growth season duration of agricultural relative to nonagricultural sites. Because the two experimental populations have histories of only 10–50 yr in the site of origin, the results provide evidence of rapid differentiation.

EXPERIMENTAL STUDIES OF ADAPTATION IN clarkia xantiana:II. FITNESS VARIATION ACROSS A SUBSPECIES BORDER

Because the range boundary is the locale beyond which a taxon fails to persist, it provides a unique opportunity for studying the limits on adaptive evolution. Adaptive constraints on range expansion are perplexing in view of widespread ecotypic differentiation by habitat and region within a species' range (regional adaptation) and rapid evolutionary response to novel environments. In this study of two parapatric subspecies, Clarkia xantiana ssp. xantiana and C. x. ssp. parviflora, we compared the fitness of population transplants within their native region, in a non-native region within the native range, and in the non-native range to assess whether range expansion might be limited by a greater intensity of selection on colonists of a new range versus a new region within the range. The combined range of the two subspecies spans a west-to-east gradient of declining precipitation in the Sierra Nevada of California, with ssp. xantiana in the west being replaced by ssp. parviflora in the east. Both subspecies had significantly higher fitness in the native range (range adaptation), whereas regional adaptation was weak and was found only in the predominantly outcrossing ssp. xantiana but was absent in the inbreeding ssp. parvifilora. Because selection intensity on transplants was much stronger in the non-native range relative to non-native regions, there is a larger adaptive barrier to range versus regional expansion. Three of five sequential fitness components accounted for regional and range adaptation, but only one of them, survivorship from germination to flowering, contributed to both. Flower number contributed to regional adaptation in ssp. xantiana and fruit set (number of fruits per flower) to range adaptation. Differential survivorship of the two taxa or regional populations of ssp. xantiana in non-native environments was attributable, in part, to biotic interactions, including competition, herbivory, and pollination. For example, low fruit set in ssp. xantiana in the east was likely due to the absence of its principal specialist bee pollinators in ssp. parviflora's range. Thus, convergence on self-fertilization may be necessary for ssp. xantiana to invade ssp. parviflora's range, but the evolution of outcrossing would not be required for ssp. parviflora to invade ssp. xantiana's range.

EXPERIMENTAL STUDIES OF ADAPTATION IN CLARKIA XANTIANA. II. FITNESS VARIATION ACROSS A SUBSPECIES BORDER

Because the range boundary is the locale beyond which a taxon fails to persist, it provides a unique opportunity for studying the limits on adaptive evolution. Adaptive constraints on range expansion are perplexing in view of widespread ecotypic differentiation by habitat and region within a species' range (regional adaptation) and rapid evolutionary response to novel environments. In this study of two parapatric subspecies, Clarkia xantiana ssp. xantiana and C. x. ssp. parviflora, we compared the fitness of population transplants within their native region, in a non-native region within the native range, and in the non-native range to assess whether range expansion might be limited by a greater intensity of selection on colonists of a new range versus a new region within the range. The combined range of the two subspecies spans a west-to-east gradient of declining precipitation in the Sierra Nevada of California, with ssp. xantiana in the west being replaced by ssp. parviflora in the east. Both subspecies had significantly higher fitness in the native range (range adaptation), whereas regional adaptation was weak and was found only in the predominantly outcrossing ssp. xantiana but was absent in the inbreeding ssp. parviflora. Because selection intensity on transplants was much stronger in the non-native range relative to non-native regions, there is a larger adaptive barrier to range versus regional expansion. Three of five sequential fitness components accounted for regional and range adaptation, but only one of them, survivorship from germination to flowering, contributed to both. Flower number contributed to regional adaptation in ssp. xantiana and fruit set (number of fruits per flower) to range adaptation. Differential survivorship of the two taxa or regional populations of ssp. xantiana in non-native environments was attributable, in part, to biotic interactions, including competition, herbivory, and pollination. For example, low fruit set in ssp. xantiana in the east was likely due to the absence of its principal specialist bee pollinators in ssp. parviflora's range. Thus, convergence on self-fertilization may be necessary for ssp. xantiana to invade ssp. parviflora's range, but the evolution of outcrossing would not be required for ssp. parviflora to invade ssp. xantiana's range.

Explaining stasis: microevolutionary studies in natural populations.

Microevolution, defined as a change in the genetic constitution of a population over time, is considered to be of commonplace occurrence in nature. Its ubiquity can be inferred from the observation that quantitative genetic divergence among populations usually exceeds that to be expected due to genetic drift alone, and from numerous observations and experiments consistent with local adaptation. Experimental manipulations in natural populations have provided evidence that rapid evolutionary responses may occur in the wild. However, there are remarkably few cases where direct observations of natural populations have revealed microevolutionary changes occurring, despite the frequent demonstration of additive genetic variation and strong directional selection for particular traits. Those few cases where responses congruent with expectation have been demonstrated are restricted to changes over one generation. In this article we focus on possible explanations as to why heritable traits under apparently strong directional selection often fail to show the expected evolutionary response. To date, few of these explanations for apparent stasis have been amenable to empirical testing. We describe new methods, derived from procedures developed by animal breeding scientists, which can be used to address these explanations, and illustrate the approach with examples from long-term studies of collared flycatchers (Ficedula albicollis) and red deer (Cervus elaphus). Understanding why most intensively studied natural populations do not appear to be evolving is an important challenge for evolutionary biology.

Rapid selection effects in a short-lived semelparous squid species exposed to exploitation: inferences from the optimisation of life-history functions

The short life span of cephalopods suggests a potential for high sensitivity to the artificial selective effects of human exploitation. To explore the effects of such selection life-history optimisation was applied using data for a semelparous squid, Illex argentinus with a life span of one year. Survival and fecundity functions were combined to generate a life time reproductive potential function. The maximum reproductive potential identified the optimum age for the squid to mature. In a situation of a constant mortality rate the maximum reproductive potential was achieved at an earlier age of maturation as mortality rate increased. The exact age when the optimum maturation occurs is sensitive to the rate of mortality and the form of the assumed growth curve but covers the age range when maturation is known to occur in this species. A more realistic seasonal fishing mortality function produced a more complex fitness curve with a temporally more restricted optimal age of maturity. The selection effects will be stronger in a seasonal fishery suggesting potentially very rapid evolutionary rates. Developing analyses specifically considering frequency-dependence and environmental-feedbacks will be valuable to clarify the potential of squid to show rapid evolutionary responses to selection. Strong selection for early age of maturation could affect the yield from the fishery but more importantly, could also make the migratory strategy, on which the fishery is based, an unviable option, resulting in collapse of the fishery that exploits the migratory component of the species.

Translocations and rapid evolutionary responses in recently established populations of western mosquitofish (Gambusia affinis)

The response of quantitative traits in translocated populations has not been well explored. Evolutionary shifts in quantitative traits, such as life history characteristics, are of particular interest because of their obvious association with fitness. In a recent survey, Stockwell (1995) examined life history variation of four populations of western mosquitofish (Gambusia affinis) that were derived from a common ancestral population 55–58 years earlier. Three life history traits differed considerably among the four sites and appeared to be correlated with local environmental conditions. To test whether these differences were due to plasticity or rapid evolution, fish from the four sites were maintained under common-garden conditions for two generations. After two generations a genetic basis was inferred for two of the three traits (size at maturity and fat content), but not for the third trait (offspring size). Thus, rapid evolution had occurred for two life history traits in these recently established populations. This case of rapid life history evolution may be due to genetic drift and/or natural selection. These data suggest that translocations may lead to rapid evolutionary responses of targeted taxa. Rapid evolutionary responses are of special concern for ‘refuge’ populations that are maintained as a hedge against extinction.