scholarly journals How does parental environment influence the potential for adaptation to global change?

2018 ◽  
Vol 285 (1886) ◽  
pp. 20181374 ◽  
Author(s):  
Evatt Chirgwin ◽  
Dustin J. Marshall ◽  
Carla M. Sgrò ◽  
Keyne Monro

Parental environments are regularly shown to alter the mean fitness of offspring, but their impacts on the genetic variation for fitness, which predicts adaptive capacity and is also measured on offspring, are unclear. Consequently, how parental environments mediate adaptation to environmental stressors, like those accompanying global change, is largely unknown. Here, using an ecologically important marine tubeworm in a quantitative-genetic breeding design, we tested how parental exposure to projected ocean warming alters the mean survival, and genetic variation for survival, of offspring during their most vulnerable life stage under current and projected temperatures. Offspring survival was higher when parent and offspring temperatures matched. Across offspring temperatures, parental exposure to warming altered the distribution of additive genetic variance for survival, making it covary across current and projected temperatures in a way that may aid adaptation to future warming. Parental exposure to warming also amplified nonadditive genetic variance for survival, suggesting that compatibilities between parental genomes may grow increasingly important under future warming. Our study shows that parental environments potentially have broader-ranging effects on adaptive capacity than currently appreciated, not only mitigating the negative impacts of global change but also reshaping the raw fuel for evolutionary responses to it.

Genetics ◽  
1998 ◽  
Vol 150 (2) ◽  
pp. 945-956 ◽  
Author(s):  
Hong-Wen Deng

Abstract Deng and Lynch recently proposed estimating the rate and effects of deleterious genomic mutations from changes in the mean and genetic variance of fitness upon selfing/outcrossing in outcrossing/highly selfing populations. The utility of our original estimation approach is limited in outcrossing populations, since selfing may not always be feasible. Here we extend the approach to any form of inbreeding in outcrossing populations. By simulations, the statistical properties of the estimation under a common form of inbreeding (sib mating) are investigated under a range of biologically plausible situations. The efficiencies of different degrees of inbreeding and two different experimental designs of estimation are also investigated. We found that estimation using the total genetic variation in the inbred generation is generally more efficient than employing the genetic variation among the mean of inbred families, and that higher degree of inbreeding employed in experiments yields higher power for estimation. The simulation results of the magnitude and direction of estimation bias under variable or epistatic mutation effects may provide a basis for accurate inferences of deleterious mutations. Simulations accounting for environmental variance of fitness suggest that, under full-sib mating, our extension can achieve reasonably well an estimation with sample sizes of only ∼2000-3000.


2021 ◽  
Author(s):  
Lisandro Milocco ◽  
Isaac Salazar-Ciudad

Predicting how populations respond to selection is a key goal of evolutionary biology. The field of quantitative genetics provides predictions for the response to directional selection through the breeder’s equation. However, differences between the observed responses to selection and those predicted by the breeder’s equation occur. The sources of these errors include omission of traits under selection, inaccurate estimates of genetic variance, and nonlinearities in the relationship between genetic and phenotypic variation. A key insight from previous research is that the expected value of these prediction errors is often not zero, in which case the predictions are systematically biased. Here, we propose that this prediction bias, rather than being a nuisance, can be used to improve the predictions. We use this to develop a novel method to predict the response to selection, which is built on three key innovations. First, the method predicts change as the breeder’s equation plus a bias term. Second, the method combines information from the breeder’s equation and from the record of past changes in the mean, to estimate the bias and predict change using a Kalman filter. Third, the parameters of the filter are fitted in each generation using a machine-learning algorithm on the record of past changes. We apply the method to data of an artificial selection experiment of the wing of the fruit fly, as well as to an in silico evolution experiment for teeth. We find that the method outperforms the breeder’s equation, and notably provides good predictions even when traits under selection are omitted from the analysis and when additive genetic variance is estimated inaccurately. The proposed method is easy to apply since it only requires recording the mean of the traits over past generations.


Genetika ◽  
2013 ◽  
Vol 45 (1) ◽  
pp. 51-62
Author(s):  
Srdjan Bojovic ◽  
Philippe Heizmann ◽  
Dragana Drazic ◽  
Dragan Kovacevic ◽  
Petar Marin ◽  
...  

PCR-RAPD markers revealed individual variation in F. ornus. A total of 122 fragments were amplified using 7 primers and of these 97 fragments were polymorphic. The percentage of polymorphic loci was between 53.3% and 74.6% with an average of 63.1%. The mean gene diversity for all populations was 0.30 and the mean Shannon?s index was 0.44. Of the total genetic variation 87% was intra-population whilst 13% was inter-population. The Mantel test revealed significant correlation between genetic and geographical distance matrice. Results herein represent the first use of molecular genetic (DNA) markers to characterize genetic variation in F. ornus populations. The partition of total genetic variance indicates a relatively restricted population differentiation as expected in outcrossing species. Present and future information on genetic structure and variability in F. ornus needs to be incorporated into strategies for the preservation of genetic resources of tree species.


2016 ◽  
Vol 6 (12) ◽  
pp. 3903-3911 ◽  
Author(s):  
Robert M Griffin ◽  
Holger Schielzeth ◽  
Urban Friberg

Abstract Theory makes several predictions concerning differences in genetic variation between the X chromosome and the autosomes due to male X hemizygosity. The X chromosome should: (i) typically show relatively less standing genetic variation than the autosomes, (ii) exhibit more variation in males compared to females because of dosage compensation, and (iii) potentially be enriched with sex-specific genetic variation. Here, we address each of these predictions for lifespan and aging in Drosophila melanogaster. To achieve unbiased estimates of X and autosomal additive genetic variance, we use 80 chromosome substitution lines; 40 for the X chromosome and 40 combining the two major autosomes, which we assay for sex-specific and cross-sex genetic (co)variation. We find significant X and autosomal additive genetic variance for both traits in both sexes (with reservation for X-linked variation of aging in females), but no conclusive evidence for depletion of X-linked variation (measured through females). Males display more X-linked variation for lifespan than females, but it is unclear if this is due to dosage compensation since also autosomal variation is larger in males. Finally, our results suggest that the X chromosome is enriched for sex-specific genetic variation in lifespan but results were less conclusive for aging overall. Collectively, these results suggest that the X chromosome has reduced capacity to respond to sexually concordant selection on lifespan from standing genetic variation, while its ability to respond to sexually antagonistic selection may be augmented.


1981 ◽  
Vol 37 (1) ◽  
pp. 79-93 ◽  
Author(s):  
Trudy F. C. Mackay

SUMMARYIn order to assess the relationship between genetic and environmental variability, a large natural population of Drosophila melanogaster was replicated as eight subpopulations, which were subjected to four different patterns of environmental variation. The environmental variable imposed was presence of 15% ethanol in the culture medium. Experimental treatments of the populations were intended to simulate constant environmental conditions, spatial heterogeneity in the environment, and two patterns of temporal environmental variation with different periodicity (long- and short-term temporal variation). Additive genetic and phenotypic variation in sternopleural and abdominal chaeta number, and body weight, were estimated in two successive years, and measurements were taken of the genotype–environment correlation of body weight and sternopleural bristle score with medium type.Additive genetic variance of sternopleural chaeta number and of body weight was significantly greater in the three populations experiencing environmental heterogeneity than in the control population, but additive genetic variance of abdominal bristle score was not clearly affected by exposing populations to varying environments. Temporal environmental variation was equally, if not more, efficient in promoting the maintenance of genetic variation than spatial heterogeneity, but the cycle length of the temporal variation was of no consequence. Specific genotype–environment interactions were not present, therefore adaptation to heterogeneous environments is by selection of heterozygosity per se, rather than by differential survival of genotypes in the alternate niches.


1982 ◽  
Vol 33 (1) ◽  
pp. 141 ◽  
Author(s):  
L Pascoe

Fleece wettability in sheep is a character believed to be related to susceptibility to fleece rot and blowfly strike. The present study was undertaken to investigate that hypothesis and to assess wettability as a possible character for a selection program. Wool samples were taken from two flocks which had been subject to selection for wool quality and resistance to fleece rot and a third flock which was unselected. The wettabilities of about 800 samples were determined. The results were found to be repeatable and the technique was capable of distinguishing between sheep. Some problems of measurement are discussed. In the one flock with a significant incidence of fleece rot, susceptibility to fleece rot was found to be associated with higher wettabilities. The mean wettability and the variance were found to be significantly higher in the unselected flock than in the two selected flocks. The heritability of wettability was estimated in the two selected flocks and was found to be low. It is argued that there is likely to be more additive genetic variance in the unselected flock and that the observed difference in wettability was due to a correlated response to selection for resistance to fleece rot. It is considered that further work on the heritability of wettability and its genetic correlations with other characters of economic importance could be fruitful.


1991 ◽  
Vol 116 (3) ◽  
pp. 580-584 ◽  
Author(s):  
Raymond O. Miller ◽  
Paul D. Bloese ◽  
James W. Hanover ◽  
Robert A. Haack

A test of Michigan half-sib progeny of paper birch (Betula papyrifera Marsh.) and European white birch (B. pendula Roth.) was conducted in Michigan to examine species variation in growth, bark color, and resistance to bronze birch borer (Agrilus anxius Gory). Paper birch was superior to European white birch in height and borer resistance at age 12 years from seed. Families of paper birch were identified that grew exceptionally well, had developed white bark within 6 years, and exhibited borer resistance. The magnitude of additive genetic variance and narrow-sense family heritability estimates for paper birch indicated that sufficient genetic variation and inheritance exist to support selection and breeding for height. Paper birch may be an acceptable substitute for European white birch as a landscape species in northeastern North America.


Genetics ◽  
1984 ◽  
Vol 108 (3) ◽  
pp. 617-632
Author(s):  
Shinichi Kusakabe ◽  
Terumi Mukai

ABSTRACT It has been reported in the previous papers of this series that in the eastern United States and Japan there is a north-to-south cline of additive genetic variance of viability and that the amount of the additive genetic variance in the northern population can be explained by mutation-selection balance. To determine whether or not the difference in the genetic variation in northern and southern populations can be explained by the differences in mutation rate and/or effective population size, numerical calculations were made using population genetic parameters. In addition, the average heterozygosities of the northern and southern populations at ten of 19 polymorphic structural loci surveyed were estimated in relation to the cline of additive genetic variance of viability, and the following findings were obtained. (1) The changes in mutation rate and population size cannot simultaneously explain the difference in additive genetic variance and inbreeding decline between the northern and southern populations. Thus, the operation of some kind of balancing selection, most likely diversifying selection, was suggested to explain the observed excess of additive genetic variance. (2) Estimates of the average heterozygosities of the southern population were not significantly different from those of the northern population. Thus, it was strongly suggested that the excess of additive genetic variance in the southern population cannot be caused by structural loci, but by factors outside the structural loci, and that protein polymorphisms are selectively neutral or nearly neutral.


2005 ◽  
Vol 56 (9) ◽  
pp. 873 ◽  
Author(s):  
Bruce Walsh

Whereas animal breeders largely focus on improvement using additive genetic variance, inbreeding and asexual reproduction allow plant breeders to at least partially exploit non-additive genetic variance as well. We briefly review various approaches used by breeders to exploit dominance and epistatic variance, discuss their constraints and limitations, and examine what (if anything) can be done to improve our ability to further use often untapped genetic variation.


Author(s):  
Bruce Walsh ◽  
Michael Lynch

Selection changes the additive-genetic variance (and hence the response in the mean) by both changing allele frequencies and by generating correlations among alleles at different loci (linkage disequilibrium). Such selection-induced correlations can be generated even between unlinked loci, and (generally) are negative, such that alleles increasing trait values tend to become increasingly negative correlated under direction or stabilizing selection, and positively correlated under disruptive selection. Such changes in the additive-genetic variance from disequilibrium is called the Bulmer effects. For a large number of loci, the amount of change can be predicted from the Bulmer equation, the analog of the breeder's equation, but now for the change in the variance. Upon cessation of selection, any disequilibrium decays away, and the variances revert back to their additive-genic variances (the additive variance in the absence of disequilibrium). Assortative mating also generates such disequilibrium.


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