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170 results for “inbreeding depression”
Data from: Evidence for inbreeding depression in a species with limited opportunity for maternal effects
It is often assumed that mating with close relatives reduces offspring fitness. In such cases, reduced offspring fitness may arise from inbreeding depression (i.e., genetic effects of elevated homozygosity) or from post-mating maternal investment. This can be due to a reduction in female investment after mating with genetically incompatible males ("differential allocation") or compensation for incompatibility ("reproductive compensation"). Here, we looked at the effects of mating with relatives on offspring fitness in mosquitofish, Gambusia holbrooki. In this species, females are assumed to be nonplacental and to allocate resources to eggs before fertilization, limiting differential allocation. We looked at the effects of mating with a brother or with an unrelated male on brood size, offspring size, gestation period, and early offspring growth. Mating with a relative reduced the number of offspring at birth, but there was no difference in the likelihood of breeding, gestation time, nor in the size or growth of these offspring. We suggest that due to limited potential for maternal effects to influence these traits that any reduction in offspring fitness, or lack thereof, can be explained by inbreeding depression rather than by maternal effects. We highlight the importance of considering the potential role of maternal effects when studying inbreeding depression and encourage further studies in other Poeciliid species with different degrees of placentation to test whether maternal effects mask or amplify any genetic effects of mating with relatives.
Data from: Scaling up the effects of inbreeding depression from individuals to metapopulations
1. Inbreeding is common in nature, and many laboratory studies have documented that inbreeding depression can reduce the fitness of individuals. Demonstrating the consequences of inbreeding depression on the growth and persistence of populations is more challenging because populations are often regulated by density- or frequency-dependent selection and influenced by demographic and environmental stochasticity. A few empirical studies have shown that inbreeding depression can increase extinction risk of local populations. The importance of inbreeding depression at the metapopulation level has been conjectured based on population-level studies but has not been evaluated. 2. We quantified the impact of inbreeding depression affecting the fitness of individuals on metapopulation persistence in heterogeneous habitat networks of different sizes and habitat configuration in a context of natural butterfly metapopulations. 3. We developed a spatial individual-based simulation model of metapopulations with explicit genetics. We used Approximate Bayesian Computation to fit the model to extensive demographic, genetic, and life-history data available for the well-studied Glanville fritillary butterfly (Melitaea cinxia) metapopulations in the Åland islands in SW Finland. We compared 18 semi-independent habitat networks differing in size and fragmentation. 4. The results show that inbreeding is more frequent in small habitat networks, and consequently, inbreeding depression elevates extinction risks in small metapopulations. Metapopulation persistence and neutral genetic diversity maintained in the metapopulations increase with the total habitat amount in and mean patch size of habitat networks. Dispersal and mating behavior interact with landscape structure to determine how likely it is to encounter kin while looking for mates. 5. Inbreeding depression can decrease the viability of small metapopulations even when they are strongly influenced by stochastic extinction-colonization dynamics and density-dependent selection. The findings from this study support that genetic factors, in addition to demographic factors, can contribute to extinctions of small local populations and also of metapopulations.
Data from: Pedigree error due to extra-pair reproduction substantially biases estimates of inbreeding depression
Understanding the evolutionary dynamics of inbreeding and inbreeding depression requires unbiased estimation of inbreeding depression across diverse mating systems. However, studies estimating inbreeding depression often measure inbreeding with error, for example, based on pedigree data derived from observed parental behavior that ignore paternity error stemming from multiple mating. Such paternity error causes error in estimated coefficients of inbreeding (f) and reproductive success and could bias estimates of inbreeding depression. We used complete "apparent" pedigree data compiled from observed parental behavior and analogous "actual" pedigree data comprising genetic parentage to quantify effects of paternity error stemming from extra-pair reproduction on estimates of f, reproductive success, and inbreeding depression in free-living song sparrows (Melospiza melodia). Paternity error caused widespread error in estimates of f and male reproductive success, causing inbreeding depression in male and female annual and lifetime reproductive success and juvenile male survival to be substantially underestimated. Conversely, inbreeding depression in adult male survival tended to be overestimated when paternity error was ignored. Pedigree error stemming from extra-pair reproduction therefore caused substantial and divergent bias in estimates of inbreeding depression that could bias tests of evolutionary theories regarding inbreeding and inbreeding depression and their links to variation in mating system.
Data from: Association between inbreeding depression and floral traits in a generalist-pollinated plant
Individual variation in the magnitude of inbreeding depression (ID) in plants and its association with phenotypic traits may have important consequences for mating system evolution. This association has been investigated only scarcely, and always considering traits functionally related to autogamy. Here, we explore the association between individual variation in ID and plant traits associated with pollinator attractiveness (related to plant size, corolla size and corolla shape) in two populations of Erysimum mediohispanicum (Brassicaceae). ID was calculated along the entire life cycle of the plants. In addition, we also explored the relationship between phenotypic traits and the individual levels of heterozygosity. We found significant associations between ID and corolla diameter and stalk height, being taller plants with larger corollas those undergoing a lower intensity of ID. Furthermore, we found a negative relationship between corolla diameter and heterozygosity, suggesting that plants with large flowers have purged their genetic load. Finally, we found a significant effect of corolla diameter on the intrapopulation genetic structure. All these findings suggest that plants with large flowers have secularly suffered frequent inbreeding in the study populations. Because corolla diameter is a trait frequently selected by pollinators in E. mediohispanicum, we believe that the observed relationship between this trait and ID could be mediated by pollinators, probably throughout an increasing in biparental inbreeding, geitonogamy or autogamy.
Data from: Phenotype-associated inbreeding biases estimates of inbreeding depression in a wild bird population
Inbreeding depression is usually quantified by regressing individual phenotypic values on inbreeding coefficients, implicitly assuming there is no correlation between an individual's phenotype and the kinship coefficient to its mate. If such an association between parental phenotype and parental kinship exists, and if the trait of interest is heritable, estimates of inbreeding depression can be biased. Here we first derive the expected bias as a function of the covariance between mean parental breeding value and parental kinship. Subsequently, we use simulated data to confirm the existence of this bias, and show that it can be accounted for in a quantitative genetic animal model. Finally, we use long-term individual-based data for white-throated dippers (Cinclus cinclus), a bird species in which inbreeding is relatively common, to obtain empirical estimate of this bias. We show that during part of the study period, parents of inbred birds had shorter wings than those of outbred birds, and as wing length is heritable, inbred individuals were smaller, independent of any inbreeding effects. This resulted in the overestimation of inbreeding effects. Similarly, during a period when parents of inbred birds had longer wings, we found that inbreeding effects were underestimated. We discuss how such associations may have arisen in this system, and why they are likely to occur in others, too. Overall, we demonstrate how less biased estimates of inbreeding depression can be obtained within a quantitative genetic framework, and suggest that inbreeding and additive genetic effects should be accounted for simultaneously whenever possible.
Data from: Strong inbreeding depression in two Scandinavian populations of the self-incompatible perennial herb Arabidopsis lyrata
Inbreeding depression is a key factor influencing mating system evolution in plants, but current understanding of its relationship with selfing rate is limited by a sampling bias with few estimates for self-incompatible species. We quantified inbreeding depression (δ) over two growing seasons in two populations of the self-incompatible perennial herb Arabidopsis lyrata ssp. petraea in Scandinavia. Inbreeding depression was strong and of similar magnitude in both populations. Inbreeding depression for overall fitness across two seasons (the product of number of seeds, offspring viability, and offspring biomass) was 81% and 78% in the two populations. Chlorophyll deficiency accounted for 81% of seedling mortality in the selfing treatment, and was not observed among offspring resulting from outcrossing. The strong reduction in both early viability and late quantitative traits suggests that inbreeding depression is due to deleterious alleles of both large and small effect, and that both populations experience strong selection against the loss of self-incompatibility. A review of available estimates suggested that inbreeding depression tends to be stronger in self-incompatible than in self-compatible highly outcrossing species, implying that undersampling of self-incompatible taxa may bias estimates of the relationship between mating system and inbreeding depression.
Data from: Using heterozygosity–fitness correlations to study inbreeding depression in an isolated population of white-tailed deer founded by few individuals
A heterozygosity–fitness correlations (HFCs) may reflect inbreeding depression, but the extent to which they do so is debated. HFCs are particularly likely to occur after demographic disturbances such as population bottleneck or admixture. We here study HFC in an introduced and isolated ungulate population of white-tailed deer Odocoileus virginianus in Finland founded in 1934 by four individuals. A total of 422 ≥ 1-year-old white-tailed deer were collected in the 2012 hunting season in southern Finland and genotyped for 14 microsatellite loci. We find significant identity disequilibrium as estimated by g2. Heterozygosity was positively associated with size- and age-corrected body mass, but not with jaw size or (in males) antler score. Because of the relatively high identity disequilibrium, heterozygosity of the marker panel explained 51% of variation in inbreeding. Inbreeding explained approximately 4% of the variation in body mass and is thus a minor, although significant source of variation in body mass in this population. The study of HFC is attractive for game- and conservation-oriented wildlife management because it presents an affordable and readily used approach for genetic monitoring that allowing identification of fitness costs associated with genetic substructuring in what may seem like a homogeneous population.
Data from: A Bayesian method for the joint estimation of outcrossing rate and inbreeding depression
The population outcrossing rate (t) and adult inbreeding coefficient (F) are key parameters in mating system evolution. The magnitude of inbreeding depression as expressed in the field can be estimated given t and F via the method of Ritland (1990). For a given total sample size, the optimal design for the joint estimation of t and F requires sampling large numbers of families (100-400) with fewer offspring (1-4) per family. Unfortunately, the standard inference procedure (MLTR) yields significantly biased estimates for t and F when family sizes are small and maternal genotypes are unknown (a common occurrence when sampling natural populations). Here, we present a Bayesian method implemented in the program BORICE that effectively estimates t and F when family sizes are small and maternal genotype information is lacking. BORICE should enable wider use of the Ritland approach for field-based estimates of inbreeding depression. As proof of concept, we estimate t and F in a natural population of Mimulus guttatus. In addition, we describe how individual maternal inbreeding histories inferred by BORICE may prove useful in studies of inbreeding and its consequences.
Data from: Loss of heterosis and family-dependent inbreeding depression in plant performance and resistance against multiple herbivores under drought stress
1. Inbreeding depression (ID), outbreeding depression (OD) and heterosis can occur concurrently in plant populations. ID often increases under environmental stress, but the combined effects of inbreeding, outbreeding between populations and environmental stress, such as drought, on plant performance and herbivore resistance remain unclear. 2. In order to determine environment-dependent and family-dependent ID, OD and heterosis we conducted a common garden experiment with plants from five populations of Brassica nigra. Inbred, within-population outbred and between-population outbred plant families were exposed to drought or ambient water levels. We recorded the abundance and damage caused by specialist herbivores from contrasting feeding guilds, i.e. the phloem-feeding Brevicoryne brassicae, the leaf-chewing Psylliodes chrysocephalus and the stem-boring Ceutorhynchus quadridens larvae. 3. Drought stress had negative effects on growth, herbivore resistance and resistance against B. brassicae and positive effects on investments in reproductive output and plant secondary metabolites (sinigrin). We found drought stress-induced loss of heterosis for plant height and investment in reproductive output. Between-population outbred plants were more sensitive to drought stress in terms of above-ground biomass compared to within-population outbred plants. 4. Drought and inbreeding synergistically negatively influenced traits related to growth and reproductive output (environment-dependent inbreeding depression, EDID). There was high variation among families within populations in the degree of ID and EDID. Genetic variation in EDID could buffer the negative effects of genetic stress associated with habitat fragmentation and concurrent environmental stress. In order to capture fully the effects of both inbreeding and between-population outbreeding under stress the different spatial scales of the effects of inbreeding and between-population outbreeding should be taken into account. 5. Synthesis. Our results indicate that drought stress influences not only inbreeding depression (ID), but also heterosis. These findings shed new light on the combined effects of anthropogenic environmental change and the genetic consequences of habitat fragmentation on plants and their interactions with other organisms. Conservation programmes aiming to restore genetically degraded populations with the translocation of individuals between populations should consider environmental stress as a risk factor.
Data from: Release from natural enemies mitigates inbreeding depression in native and invasive Silene latifolia populations
Inbreeding and enemy infestation are common in plants and can synergistically reduce their performance. This inbreeding × environment (I×E) interaction may be of particular importance for the success of plant invasions if introduced populations experience a release from attack by natural enemies relative to their native conspecifics. Here, we investigate whether inbreeding affects plant infestation damage, whether inbreeding depression in growth and reproduction is mitigated by enemy release and whether this effect is more pronounced in invasive than native plant populations. We used the invader Silene latifolia and its natural enemies as a study system. We performed two generations of experimental out- and inbreeding within eight native (European) and eight invasive (North American) populations under controlled conditions using field-collected seeds. Subsequently, we exposed the offspring to an enemy exclusion and inclusion treatment in a common garden in the species' native range to assess the interactive effects of population origin (range), breeding treatment and enemy treatment on infestation damage, growth and reproduction. Inbreeding increased flower and leaf infestation damage in plants from both ranges, but had opposing effects on fruit damage in native versus invasive plants. Inbreeding significantly reduced plant fitness, whereby inbreeding depression in fruit number was higher in enemy inclusions than exclusions. This effect was equally pronounced in populations from both distribution ranges. Moreover, the magnitude of inbreeding depression in fruit number was lower in invasive than native populations. These results support that inbreeding has the potential to reduce plant defenses in S. latifolia, which magnifies inbreeding depression in the presence of enemies. However, future studies are necessary to further explore whether enemy release in the invaded habitat has actually decreased inbreeding depression and thus facilitated the persistence of inbred founder populations and invasion success. In addition, our findings emphasize the importance of purging for for successful range expansion.
Data from: Molecular and quantitative signatures of biparental inbreeding depression in the self-incompatible tree species Prunus avium
Genetic diversity strongly influences populations' adaptability to changing environments and therefore survival. Sustainable forest management practices have multiple roles including conservation of genetic resources and timber production. In this study, we aimed at better understanding the variation in genetic diversity among adult and offspring individuals, and the effects of mating system on offspring survival and growth in wild cherry, Prunus avium. We analysed adult trees and open pollinated seed-families from three stands in Germany at eight microsatellite loci and one incompatibility system locus and conducted paternity analyses. Seed viability testing and seed sowing in a nursery allowed further testing for the effects of pollen donor diversity and genetic similarity between mates on the offspring performance at the seed and seedling stages. Our results were contrasting across stands. Loss of genetic diversity from adult to seedling stages and positive effect of mate diversity on offspring performance occurred in one stand only, whereas biparental inbreeding depression and significant decrease in fixation index from adults to seedlings was detected in two stands. We discussed the effects of stand genetic diversity on the magnitude of biparental inbreeding depression at several life-stages and its consequences on the management of genetic resources in P. avium.
Data from: Relative risks of inbreeding and outbreeding depression in the wild in endangered salmon
Conservation biologists routinely face the dilemma of keeping small, fragmented populations isolated, wherein inbreeding depression may ensue, or mixing such populations, which may exacerbate population declines via outbreeding depression. The joint evaluation of inbreeding and outbreeding risks in the wild cannot be readily conducted in endangered species, so a suggested 'safe' strategy is to mix ecologically and genetically similar populations. To evaluate this strategy, we carried out a reciprocal transplant experiment involving three neighbouring populations of endangered Atlantic salmon (Salmo salar) now bred in captivity and maintained in captive and wild environments. Pure, inbred, and outbred (first and second generation) cross types were released and recaptured in the wild to simultaneously test for local adaptation, inbreeding depression and outbreeding depression. We found little evidence of inbreeding depression after one generation of inbreeding and little evidence of either heterosis or outbreeding depression via genetic incompatibilities after one or two generations of outbreeding. A trend for outbreeding depression via the loss of local adaptation was documented in one of three populations. The effects of inbreeding were not significantly different from the effects of outbreeding. Hence, at the geographic scale evaluated (34-50 km), inbreeding for one generation and outbreeding over two generations may have similar effects on the persistence of small populations. The results further suggested that outbreeding outcomes may be highly variable or unpredictable at small genetic distances. Our work highlights the necessity of evaluating the relative costs of inbreeding and outbreeding in the conservation and management of endangered species on a case-by-case basis.
Data from: Inbreeding and inbreeding depression of early life traits in a cooperative mammal
Mating between relatives often results in negative fitness consequences or inbreeding depression. However, the expression of inbreeding in populations of wild cooperative mammals and the effects of environmental, maternal and social factors on inbreeding depression in these systems are currently not well understood. This study uses pedigree-based inbreeding coefficients from a long-term study of meerkats (Suricata suricatta) in South Africa to reveal that 44% of the population have detectably non-zero (F>0) inbreeding coefficients. 15% of these inbred individuals were the result of moderate inbreeding (F≥0.125), although such inbreeding events almost solely occurred when mating individuals had no prior experience of each other. Inbreeding depression was evident for a range of traits: pup mass at emergence from the natal burrow, hind-foot length, growth until independence and juvenile survival. However, we found no evidence of significant inbreeding depression for skull and forearm length or for pup survival. This research provides a rare investigation into inbreeding in a cooperative mammal, revealing high levels of inbreeding, considerable negative consequences and complex interactions with the social environment.
Data from: Inbreeding depression by environment interactions in a free-living mammal population
Experimental studies often find that inbreeding depression is more severe in harsh environments, but the few studies of in situ wild populations available to date rarely find strong support for this effect. We investigated evidence for inbreeding depression by environment interactions in nine traits in the individually monitored Soay sheep population of St Kilda, using genomic inbreeding coefficients based on 37 037 single-nucleotide polymorphism loci, and population density as an axis of environmental variation. All traits showed variation with population density and all traits showed some evidence for depression because of either an individual's own inbreeding or maternal inbreeding. However, only six traits showed evidence for an interaction in the expected direction, and only two interactions were statistically significant. We identify three possible reasons why wild population studies may generally fail to find strong support for interactions between inbreeding depression and environmental variation compared with experimental studies. First, for species with biparental inbreeding only, the amount of observed inbreeding in natural populations is generally low compared with that used in experimental studies. Second, it is possible that experimental studies sometimes actually impose higher levels of stress than organisms experience in the wild. Third, some purging of the deleterious recessive alleles that underpin interaction effects may occur in the wild.
Data from: Sex-specific inbreeding depression depends on the strength of male-male competition
Inbreeding depression has become a central theme in evolutionary biology and is considered to be a driving force for the evolution of reproductive morphology, physiology, behavior, and mating systems. Despite the overwhelming body of empirical work on the reproductive consequences of inbreeding, relatively little is known on whether inbreeding depresses male and female fitness to the same extent. However, sex-specific inbreeding depression has been argued to affect the evolution of selfing rates in simultaneous hermaphrodites and provides a powerful approach to test whether selection is stronger in males than in females, which is predicted to be the consequence of sexual selection. We tested for sex-specific inbreeding depression in the simultaneously hermaphroditic freshwater snail Physa acuta by comparing the reproductive performance of both sex functions between selfed and outcrossed focal individuals under different levels of male–male competition. We found that inbreeding impaired both male and female reproductive success and that the magnitude of male inbreeding depression exceeded female inbreeding depression when the opportunity for sperm competition was highest. Our study provides the first evidence for sex-specific inbreeding depression in a hermaphroditic animal and highlights the importance of considering the level of male–male competition when assessing sex differences in inbreeding depression.
Stresses affect inbreeding depression in complex ways: Disentangling stress-specific genetic effects from effects of initial size in plants
<p>The magnitude of inbreeding depression (ID) varies unpredictably among environments. ID often increases in stressful environments suggesting that these expose more deleterious alleles to selection or increase their effects. More simply, ID could increase under conditions that amplify phenotypic variation (CV²), e.g. by accentuating size hierarchies among plants. These mechanisms are difficult to distinguish when stress increases both ID and phenotypic variation. We grew in- and outbred progeny of <i>Mimulus guttatus</i> under six abiotic stress treatments (control, waterlogging, drought, nutrient deficiency, copper addition and clipping) with and without competition by the grass <i>Poa palustris</i>. ID differed greatly among stress treatments with δ varying from 7% (control) to 61% (waterlogging) but did not consistently increase with stress intensity. <i>Poa</i> competition increased ID under nutrient deficiency but not other stresses. Analyzing effects of initial size on performance of outbred plants suggests that under some conditions (low N, clipping) competition increased ID by amplifying initial size differences. In other cases (e.g., high ID under waterlogging), particular environments amplified the deleterious genetic effects of inbreeding suggesting differential gene expression. Interestingly, conditions that increased the phenotypic variability of inbred progeny regularly increased ID whereas variability among outbred progeny showed no relationship to ID. Our study reconciles the stress- and phenotypic variability hypotheses by demonstrating how specific conditions (rather than stress <i>per se</i>) act to increase ID. Analyzing CV² separately in inbred and outbred progeny while including effects of initial plant size improve our ability to predict how ID and gene expression vary across environments.</p>
Data from: Inbreeding, inbreeding depression and infidelity in a cooperatively-breeding bird
Inbreeding depression plays a major role in shaping mating systems: in particular, inbreeding avoidance is often proposed as a mechanism explaining extra-pair reproduction in socially-monogamous species. This suggestion relies on assumptions which are rarely comprehensively tested: that inbreeding depression is present, that higher kinship between social partners increases infidelity, and that infidelity reduces the frequency of inbreeding. Here, we test these assumptions using 26 years of data for a cooperatively-breeding, socially-monogamous bird with high female infidelity, the superb fairy-wren (Malurus cyaneus). Although inbred individuals were rare (~6% of offspring), we found evidence of inbreeding depression in nestling mass (but not in fledgling survival). Mother-son social pairings resulted in 100% infidelity, but kinship between a social pair did not otherwise predict female infidelity. Nevertheless, extra-pair offspring were less likely to be inbred than within-pair offspring. Finally, the social environment (the number of helpers in a group) did not affect offspring inbreeding coefficients or inbreeding depression levels. In conclusion, despite some agreement with the assumptions that are necessary for inbreeding avoidance to drive infidelity, the apparent scarcity of inbreeding events and the observed levels of inbreeding depression seem insufficient to explain the ubiquitous infidelity in this system, beyond the mother-son mating avoidance.
Data from: Inbreeding depression changes with stress response over time in flooded Mimulus guttatus
<p><strong>Abstract</strong></p> <p>Inbreeding usually reduces offspring fitness (‘inbreeding depression’, ID), and may affect the plasticity of functional traits involved in the response to stress. ID is often found to increase under stress, but there are also reports of no effects or even a reduction of ID under stress. One reason for this variation that has received little attention may be related to different concepts of stress. In particular, the magnitude of ID may be unrelated to the effect of an environment on fitness (evolutionary stress concept), but increase particularly during the ‘alarm phase’ after a stress has been initiated (physiological stress concept). We clonally replicated inbred and outbred <em>Mimulus guttatus</em> plants, for which ID was known to increase under flooding. We exposed the clonal replicates to control and flooding conditions and harvested replicates of each genotype after two, six and 11 weeks of growth. As functional traits related to stress response we measured chlorophyll fluorescence, root mass and the production of stolons and adventitious roots. As fitness estimates we measured biomass and flower number, and we pollinated a subset of plants and grew a second generation of plants under control and flooding conditions to calculate multiplicative fitness. Overall, <em>M. guttatus</em> proved to be very flooding-tolerant. Chlorophyll fluorescence (F<sub>v</sub>/F<sub>m</sub>) was not influenced by flooding, but decreased with leaf age and increased after fertilization. At the end of the experiment, biomass and flower number (F<sub>1</sub> generation) as well as multiplicative fitness (including performance in the F<sub>2</sub> generation) were even higher under flooding than under control conditions. Flooding reduced the root mass in the pots, but increased the production of stolons and floating roots. Plasticity in these traits can be regarded as beneficial, although selection gradient analysis failed to identify plasticity in stolon number as adaptive. Only two functional traits were influenced by an interaction between flooding and inbreeding, early stolon length (suggesting a reduced flooding escape response of inbred plants) and root tissue density of floating adventitious roots (suggesting a reduced aeration of the roots of inbred offspring). ID in fitness-related traits was higher under flooding, but its magnitude changed strongly over the course of the experiment. ID under flooding was particularly high after two weeks (δ = 0.42 vs. 0.05 in the control), suggesting sensitivity of inbred plants to the initiation of flooding (‘alarm phase’ of stress response). This effect had disappeared after 6 weeks when plants had acclimated to ongoing flooding. However, under flooding ID increased again after 11 weeks, this time because outbred plants grew much better under flooded than control conditions, and the same pattern was found for the multiplicative fitness function (δ = 0.68 under flooding vs. 0.36 in the control). Our results suggest that ID was higher under flooding, but not because this environment was generally more stressful. Instead, at an early stage ID increased because inbred offspring was more sensitive to the physiological stress after the initiation of flooding (‘alarm phase’), whereas at a late stage ID increased because outbred offspring was more capable of exploiting the favourable flooding conditions. In general, our results show that phenotypic plasticity may often be robust against the effects of inbreeding. Moreover, ID may increase in particular under conditions of physiological stress, during which many stress-specific genes are expressed, whereas ID may not necessarily increase under constant poor conditions that reduce fitness, even if the stress is very strong in the evolutionary sense.</p>
Data from: Genomic analysis reveals depression due to both individual and maternal inbreeding in a free-living mammal population
There is ample evidence for inbreeding depression manifested as a reduction in fitness or fitness-related traits in the focal individual. In many organisms, fitness is not only affected by genes carried by the individual, but also by genes carried by their parents, for example if receiving parental care. While maternal effects have been described in many systems, the extent to which inbreeding affects fitness directly through the focal individual, or indirectly through the inbreeding coefficients of its parents, has rarely been examined jointly. The Soay sheep study population is an excellent system in which to test for both effects, as lambs receive extended maternal care. Here, we tested for both maternal and individual inbreeding depression in three fitness-related traits (birthweight and weight and hindleg length at 4 months of age) and three fitness components (first-year survival, adult annual survival and annual breeding success), using either pedigree-derived inbreeding or genomic estimators calculated using ~37 000 SNP markers. We found evidence for inbreeding depression in 4-month hindleg and weight, first-year survival in males, and annual survival and breeding success in adults. Maternal inbreeding was found to depress both birthweight and 4-month weight. We detected more instances of significant inbreeding depression using genomic estimators than the pedigree, which is partly explained through the increased sample sizes available. In conclusion, our results highlight that cross-generational inbreeding effects warrant further exploration in species with parental care and that modern genomic tools can be used successfully instead of, or alongside, pedigrees in natural populations.
Data from: Inter-population variation in mating system and late-stage inbreeding depression in Magnolia stellata
Inbreeding has the potential to cause evolutionary changes in populations, although these changes are likely to drive populations to extinction through inbreeding depression and reductions in genetic diversity. We investigated the mating system and late-stage inbreeding depression (δ) in 10 populations of Magnolia stellata using nine microsatellite markers and evaluated the effects of population size and the degree of population isolation through inbreeding and inbreeding depression on the persistence of populations. The outcrossing rates were very similar (~0.7) among populations, but the correlations of paternity, fractions of biparental inbreeding and inbreeding coefficients at the seed stage (FS) varied among populations, suggesting that the level of outcrossing was similar among populations, while the quality of it was not. A significant negative correlation was detected between FS and population size. The average value of δ was 0.709, and the values in six of the 10 populations were significant. The values of δ differed among populations, although clear relationships with population size and the degree of population isolation were not detected. However, in one population, which was very small and located in the edge of the species' range, we obtained a very low value of δ (-0.096), which may be indicative of purging or the fixation of deleterious alleles. Existing M. stellata populations that are small (and thus might be expected to have higher frequencies of inbreeding) and have large values of δ may be in danger of declining, even if the populations are located within the central region of the species range.
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