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Environmental Variance (environmental + variance)
Selected AbstractsEnvironmental variance, population growth and evolutionJOURNAL OF ANIMAL ECOLOGY, Issue 1 2010Shripad Tuljapurkar N. Jonzén, T. Pople, K. Knape & M. Skjöld (2009) Stochastic demography and population dynamics in the red kangaroo (Macropus rufus). Journal of Animal Ecology, 79, 109,116. Environmental fluctuations on time scales of one to tens of generations are increasingly recognized as important determinants of population dynamics and microevolution. Jonzén et al. in this issue analyse how the vital rates of red kangaroos depend on annual rainfall, and estimate the elasticities of stochastic growth rate to the means and variances of the vital rates, as well as to the mean and variance of rainfall. Their results demonstrate how ecological and evolutionary studies can benefit from including explicit environmental drivers when modelling populations, and from the use of mean and variance elasticities. [source] Estimating the growth of a newly established moose population using reproductive valueECOGRAPHY, Issue 3 2007Bernt-Erik Sæther Estimating the population growth rate and environmental stochasticity of long-lived species is difficult because annual variation in population size is influenced by temporal autocorrelations caused by fluctuations in the age-structure. Here we use the dynamics of the reproductive value to estimate the long-term growth rate s and the environmental variance of a moose population that recently colonized the island of Vega in northern Norway. We show that the population growth rate was high (,=0.26). The major stochastic influences on the population dynamics were due to demographic stochasticity, whereas the environmental variance was not significantly different from 0. This supports the suggestion that population growth rates of polytocous ungulates are high, and that demographic stochasticity must be assessed when estimating the growth of small ungulate populations. [source] Modeling the genetic and environmental association between peer group deviance and cannabis use in male twinsADDICTION, Issue 3 2009Nathan A. Gillespie ABSTRACT Background Peer group deviance (PGD) is linked strongly to liability to drug use, including cannabis. Our aim was to model the genetic and environmental association, including direction of causation, between PGD and cannabis use (CU). Method Results were based on 1736 to 1765 adult males from the Mid-Atlantic Twin Registry with complete CU and PGD data measured retrospectively at three time-intervals between 15 and 25 years using a life-history calendar. Results At all ages, multivariate modeling showed that familial aggregation in PGD was explained by a combination of additive genetic and shared environmental effects. Moreover, the significant PGD,CU association was best explained by a CU,PGD causal model in which large portions of the additive genetic (50,78%) and shared environmental variance (25,73%) in PGD were explained by CU. Conclusions Until recently PGD was assumed to be an environmental, upstream risk factor for CU. Our data are not consistent with this hypothesis. Rather, they suggest that the liability to affiliate with deviant peers is explained more clearly by a combination of genetic and environmental factors that are indexed by CU which sits as a ,risk indicator' in the causal pathway between genetic and environmental risks and the expression of PGD. This is consistent with a process of social selection by which the genetic and environmental risks in CU largely drive the propensity to affiliate with deviant peers. [source] Personality and marital satisfaction: a behavioural genetic analysisEUROPEAN JOURNAL OF PERSONALITY, Issue 3 2005Erica L. Spotts Previous research has found that genetic and nonshared environmental factors influence marital quality (Spotts et al., 2004). The current study explored personality as a source for these genetic and environmental individual differences. A sample of 752 Swedish twin women and their spouses were used. Genetic and environmental influences were found for self-report measures of marital quality, but only environmental factors contributed to the variance of observational measures of marital quality. Wives' personality characteristics accounted for genetic and nonshared environmental variance in the wives' own marital satisfaction, their husbands' marital satisfaction, and the agreement between the spouses on the quality of their marriage. Genetic influences on the correlation between wives' genetically influenced personality characteristics and their husbands' marital satisfaction indicate a gene,environment correlation. Contrary to expectations, husbands' personality did not explain large portions of wives' marital satisfaction beyond that explained by wives' personality. This study emphasizes the importance of spousal personality to the well-being of marriages, and results are discussed within the context of three different theories regarding associations between personality and marital quality. Copyright © 2005 John Wiley & Sons, Ltd. [source] THE PHENOTYPIC VARIANCE WITHIN PLASTIC TRAITS UNDER MIGRATION-MUTATION-SELECTION BALANCEEVOLUTION, Issue 6 2006Xu-Sheng Zhang Abstract How phenotypic variances of quantitative traits are influenced by the heterogeneity in environment is an important problem in evolutionary biology. In this study, both genetic and environmental variances in a plastic trait under migration-mutation-stabilizing selection are investigated. For this, a linear reaction norm is used to approximate the mapping from genotype to phenotype, and a population of clonal inheritance is assumed to live in a habitat consisting of many patches in which environmental conditions vary among patches and generations. The life cycle is assumed to be selection-reproduction-mutation-migration. Analysis shows that phenotypic plasticity is adaptive if correlations between the optimal phenotype and environment have become established in both space and/or time, and it is thus possible to maintain environmental variance (VE) in the plastic trait. Under the special situation of no mutation but maximum migration such that separate patches form an effective single-site habitat, the genotype that maximizes the geometric mean fitness will come to fixation and thus genetic variance (VG) cannot be maintained. With mutation and/or restricted migration, VG can be maintained and it increases with mutation rate but decreases with migration rate; whereas VE is little affected by them. Temporal variation in environmental quality increases VG while its spatial variance decreases VG. Variation in environmental conditions may decrease the environmental variance in the plastic trait. [source] Distribution of benthic diatoms in U.S. rivers in relation to conductivity and ionic compositionFRESHWATER BIOLOGY, Issue 8 2003Marina Potapova Summary 1We quantified the relationships between diatom relative abundance and water conductivity and ionic composition, using a dataset of 3239 benthic diatom samples collected from 1109 river sites throughout the U.S.A. [U.S. Geological Survey National Water-Quality Assessment (NAWQA) Program dataset]. This dataset provided a unique opportunity to explore the autecology of freshwater diatoms over a broad range of environmental conditions. 2Conductivity ranged from 10 to 14 500 ,S cm,1, but most of the rivers had moderate conductivity (interquartile range 180,618 ,S cm,1). Calcium and bicarbonate were the dominant ions. Ionic composition, however, varied greatly because of the influence of natural and anthropogenic factors. 3Canonical correspondence analysis (CCA) and Monte Carlo permutation tests showed that conductivity and abundances of major ions (HCO + CO, Cl,, SO, Ca2+, Mg2+, Na+, K+) all explained a statistically significant amount of the variation in assemblage composition of benthic diatoms. Concentrations of HCO + CO and Ca2+ were the most significant sources of environmental variance. 4The CCA showed that the gradient of ionic composition explaining most variation in diatom assemblage structure ranged from waters dominated by Ca2+ and HCO + CO to waters with higher proportions of Na+, K+, and Cl,. The CCA also revealed that the distributions of some diatoms correlated strongly with proportions of individual cations and anions, and with the ratio of monovalent to divalent cations. 5We present species indicator values (optima) for conductivity, major ions and proportions of those ions. We also identify diatom taxa characteristic of specific major-ion chemistries. These species optima may be useful in future interpretations of diatom ecology and as indicator values in water-quality assessment. [source] An examination of the overlap between genetic and environmental risk factors for intentional weight loss and overeatingINTERNATIONAL JOURNAL OF EATING DISORDERS, Issue 6 2009Tracey D. Wade PhD Abstract Objective: To further our understanding of how intentional weight loss (IWL) and overeating are related, we examined the shared genetic and environmental variance between lifetime IWL and overeating. Method: Interview data were available for 1,976 female twins (both members of 439 and 264 pairs of monozygotic and dizygotic twins, respectively), mean age = 40.61, SD = 4.72. We used lifetime diagnostic data for eating disorders obtained from a semistructured psychiatric telephone interview, examined in a bivariate twin analysis. Both lifetime behaviors were measured on a 3-point scale, where absence of IWL or overeating formed one anchor on the scale and lifetime anorexia nervosa (AN) and bulimia nervosa (BN) formed the opposite anchors, respectively. Results: In line with previous findings, a higher body mass index was significantly associated with the lifetime presence of IWL and/or overeating (odds ratio = 1.13, 95% confidence interval (CI): 1.08,1.19). The best fitting twin model contained additive genetic and nonshared environmental influence influencing both IWL and overeating, with correlations between these influences of 0.61 (95% CI: 0.35,0.92) and 0.24 (95% CI: 0.07,0.42), respectively. Discussion: About 37% of genetic risk factors were considered to overlap between IWL and overeating, and with only 6% of overlap between environmental risk factors. Thus, considerable independence of risk factors was indicated. © 2009 by Wiley Periodicals, Inc. Int J Eat Disord 2009 [source] Genetic parameters for individual birth and weaning weight and for litter size of Large White pigsJOURNAL OF ANIMAL BREEDING AND GENETICS, Issue 3 2000D. Kaufmann Summary Data from a French experimental herd recorded between 1990 and 1997 were used to estimate genetic parameters for individual birth and weaning weight, as well as litter size of Large White pigs using restricted maximum likelihood (REML) methodology applied to a multivariate animal model. In addition to fixed effects the model included random common environment of litter, direct and maternal additive genetic effects. The data consisted of 1928 litters including individual weight observations from 18151 animals for birth weight and from 15360 animals for weaning weight with 5% of animals transferred to a nurse. Estimates of direct and maternal heritability and proportion of the common environmental variance for birth weight were 0.02, 0.21 and 0.11, respectively. The corresponding values for weaning weight were 0.08, 0.16 and 0.23 and for litter size 0.22, 0.02 and 0.06, respectively. The direct and the maternal genetic correlations between birth and weaning weight were positive (0.59 and 0.76). Weak positive (negative) genetic correlations between direct effects on weight traits and maternal effects on birth weight (weaning weight) were found. Negative correlations were found between direct genetic effect for litter size and maternal genetic effects on all three traits. The negative relationship between litter size and individual weight requires a combined selection for litter size and weight. Zusammenfassung Daten einer französischen Versuchsherde aus den Jahren 1990 bis 1997 wurden für die Schätzung von genetischen Parametern für individuelles Geburts-, Absetzgewicht und Wurfgrösse bei französischen Large White verwendet. Die Schätzung der Parameter erfolgte mit der Restricted Maximum Likelihood Methode (REML) angewandt auf ein multivariates Tiermodell. Neben fixen Effekten berücksichtigte das Modell die zufällige gemeinsame Wurfumwelt und direkte und maternale additiv genetische Effekte. Der Datensatz bestand aus 1928 Wurfaufzeichnungen mit Angaben zum individuellen Geburtsgewicht von 18151 Tieren und zum Absetzgewicht von 15360 Tieren. Nach der Geburt wurden 5% der Ferkel in einen anderen Wurf versetzt. Die geschätzten Werte für die direkte, die maternale Heritabilität und den Varianzanteil der Wurfumwelt waren für das Geburtsgewicht 0.02, 0.21 und 0.11. Die entsprechenden Werte für das Absetzgewicht waren 0.08, 0.16 und 0.23 und für die Wurfgrösse 0.22, 0.02 und 0.06. Die direkten und die maternalen genetischen Korrelationen zwischen Geburts-und Absetzgewicht waren positiv (0.59 und 0.76). Schwache positive (negative) genetische Korrelationen wurden zwischen den direkten genetischen Effekten auf die Gewichtsmerkmale und dem maternalen genetischen Effekt auf das Geburtsgewicht (Absetzgewicht) gefunden. Negative Korrelationen gab es zwischen dem direkten genetischen Effekt auf die Wurfgrösse und den maternalen genetischen Effekten auf alle drei Merkmale. Die negative Beziehung zwischen Wurfgrösse und individuellem Gewicht verlangt nach einer kombinierten Selektion für Wurfgrösse und Gewicht. [source] Heritable variation and genetic correlation of quantitative traits within and between ecotypes of Avena barbataJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 3 2008K. M. GARDNER Abstract We examined heritable variation for quantitative traits within and between naturally occurring mesic and xeric ecotypes of the slender wild oat (Avena barbata), and in 188 recombinant inbred lines derived from a cross between the ecotypes. We measured a suite of seedling and adult traits in the greenhouse, as well as performance-related traits in field sites native to the two ecotypes. Although the ecotypes were genetically diverged for most traits, few traits showed significant heritable variation within either ecotype. In contrast, considerable heritable variation was released in the recombinant progeny of the cross, and transgressive segregation was apparent in all traits. Heritabilities were substantially greater in the greenhouse than in the field, and this was associated with an increase in environmental variance in the field, rather than a decrease in genetic variance. Strong genetic correlations were evident among the recombinants, such that 22 measured traits could be well represented by only seven underlying factors, which accounted for 80% of the total variation. The primary axis of variation in the greenhouse described a trade-off between vegetative and reproductive allocation, mediated by the date of first flowering, and fitness was strongly correlated with this trade-off. Other factors in the greenhouse described variation in size and in seedling traits. Lack of correlation among these factors represents the release of multivariate trait variation through recombination. In the field, a separate axis of variation in overall performance was found for each year/site combination. Performance was significantly correlated across field environments, but not significantly correlated between greenhouse and field. [source] The continuity of microevolution and macroevolutionJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 5 2002Andrew M. Simons Abstract A persistent debate in evolutionary biology is one over the continuity of microevolution and macroevolution , whether macroevolutionary trends are governed by the principles of microevolution. The opposition of evolutionary trends over different time scales is taken as evidence that selection is uncoupled over these scales. I argue that the paradox inferred by trend opposition is eliminated by a hierarchical application of the ,geometric-mean fitness' principle, a principle that has been invoked only within the limited context of microevolution in response to environmental variance. This principle implies the elimination of well adapted genotypes , even those with the highest arithmetic mean fitness over a shorter time scale. Contingent on premises concerning the temporal structure of environmental variance, selectivity of extinction, and clade-level heritability, the evolutionary outcome of major environmental change may be viewed as identical in principle to the outcome of minor environmental fluctuations over the short-term. Trend reversals are thus recognized as a fundamental property of selection operating at any phylogenetic level that occur in response to event severities of any magnitude over all time scales. This ,bet-hedging' perspective differs from others in that a specified, single hierarchical selective process is proposed to explain observed hierarchical patterns of extinction. [source] Genetic and environmental effects on morphology and fluctuating asymmetry in nestling barn swallowsJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 3 2000Cadée A barn swallow Hirundo rustica partial cross-fostering experiment with simultaneous brood size manipulation was conducted in two years with contrasting weather conditions, to estimate heritable variation in tarsus, tail and wing size and fluctuating asymmetry. Environmental stress had contrasting effects depending on trait type. Significant heritabilities for tarsus, tail and wing size were found only in enlarged broods irrespective of year effects, while tarsus asymmetry was significantly heritable in the year with benign weather conditions irrespective of brood size manipulation effects. Tail, wing and composite (multicharacter) asymmetry were never significantly heritable. The environment with the higher heritability generally had higher additive genetic variance and lower environmental variance, irrespective of trait type. Heritability was larger for trait size than for trait asymmetry. Patterns of genetic variation in nestlings do not necessarily translate to the juvenile or adult stage, as indicated by lack of correlation between nestling and fledgling traits. [source] Evidence for an Interaction Between Age at First Drink and Genetic Influences on DSM-IV Alcohol Dependence SymptomsALCOHOLISM, Issue 12 2009Arpana Agrawal Background:, Research suggests that individuals who start drinking at an early age are more likely to subsequently develop alcohol dependence. Twin studies have demonstrated that the liability to age at first drink and to alcohol dependence are influenced by common genetic and environmental factors, however, age at first drink may also environmentally mediate increased risk for alcohol dependence. In this study, we examine whether age at first drink moderates genetic and environmental influences, via gene × environment interactions, on DSM-IV alcohol dependence symptoms. Methods:, Using data on 6,257 adult monozygotic and dizygotic male and female twins from Australia, we examined the extent to which age at first drink (i) increased mean alcohol dependence symptoms and (ii) whether the magnitude of additive genetic, shared, and nonshared environmental influences on alcohol dependence symptoms varied as a function of decreasing age. Twin models were fitted in Mx. Results:, Risk for alcohol dependence symptoms increased with decreasing age at first drink. Heritable influences on alcohol dependence symptoms were considerably larger in those who reported an age at first drink prior to 13 years of age. In those with later onset of alcohol use, variance in alcohol dependence was largely attributable to nonshared environmental variance (and measurement error). This evidence for unmeasured gene × measured environment interaction persisted even when controlling for the genetic influences that overlapped between age at first drink and alcohol dependence symptoms. Conclusions:, Early age at first drink may facilitate the expression of genes associated with vulnerability to alcohol dependence symptoms. This is important to consider, not only from a public health standpoint, but also in future genomic studies of alcohol dependence. [source] Inclusive heritability: combining genetic and non-genetic information to study animal behavior and cultureOIKOS, Issue 2 2010Étienne Danchin Phenotypic variance results from variation in biological information possessed by individuals. Quantitative geneticists often strive to partition out all environmental variance to measure heritability. Behavioral biologists and ecologists however, require methods to integrate genetic and environmental components of inherited phenotypic variance in order to estimate the evolutionary potential of traits, which encompasses any form of information that is inherited. To help develop this integration, we build on the tools of quantitative genetics and offer the concept of ,inclusive heritability' which identifies and unifies the various mechanisms of information transmission across generations. A controversial component of non-genetic information is animal culture, which is the part of phenotypic variance inherited through social learning. Culture has the unique property of being transmitted horizontally and obliquely, as well as vertically. Accounting for cultural variation would allow us to examine a broader range of evolutionary mechanisms. Culture may, for instance, produce behavioral isolating mechanisms leading to speciation. To advance the study of animal culture, we offer a definition of culture that is rooted in quantitative genetics. We also offer four testable criteria to determine whether a trait is culturally inherited. These criteria may constitute a conceptual tool to study animal culture. We briefly discuss methods to partition out cultural variance. Several authors have recently called for ,modernizing the modern synthesis' by including non-genetic factors such as epigenetics and phenotypic plasticity in order to more fully explain phenotypic evolution. Here, we further propose to broaden the concept of inheritance by incorporating the cultural component of behavior. Applying the concept of inclusive heritability may advance the integration of multiple forms of inheritance into the study of evolution. [source] Stability of genetic influences on pulmonary function in a longitudinal study of octogenarian twinsAMERICAN JOURNAL OF HUMAN BIOLOGY, Issue 3 2010Terrie Vasilopoulos Using data from the first four waves of the OCTO-Twin study (twins 80 + years), the present study investigated the stability and change of genetic and environmental contributions to pulmonary function. Using a genetic simplex model, variance in peak expiratory flow (PEF) at each wave was decomposed into additive genetic and nonshared (specific) environmental factors. Additionally, this analysis distinguished the source of these influences, either from previous waves (transmissions) or from novel influences at each wave (innovations). At each time point (except wave 1), the genetic variance was due to genetic transmissions from prior time points. Conversely, the specific environmental variance in PEF at each time point was mainly due to environmental innovations. These results imply that genetic factors contribute to the stability of pulmonary function over time whereas environmental factors contribute to its change. Am. J. Hum. Biol., 2010. © 2009 Wiley-Liss, Inc. [source] Discovery of male sterile plants and their contrasting occurrence between self-compatible and self-incompatible populations of the hermaphroditic perennial Trillium camschatcensePLANT SPECIES BIOLOGY, Issue 3 2009SHOSEI KUBOTA Abstract The sex type of Trillium camschatcense has been considered to be strictly monomorphic, composed of only hermaphroditic individuals. However, field observations have detected anther-degenerated (AD) plants coexisting with hermaphrodites. The present study aimed to elucidate whether AD plants could be regarded as females and, if so, how their loss of male function is compensated. Because T. camschatcense retains both self-compatible (SC) and self-incompatible (SI) populations, the frequencies of AD plants in multiple populations (22 SC and eight SI) were examined to predict the fate of these individuals under contrasting breeding systems. Morphological and genetic analyses in a SC population demonstrated that AD plants were completely male sterile, but female fertile. Although the quantity of seed produced was similar, hermaphrodites produced seeds predominantly via selfing, whereas seeds of AD plants were entirely outcrossed. Because inbreeding depression was severe, AD plants achieved a fitness advantage through inbreeding avoidance. However, the frequency of AD plants varied among SC populations (0,42%), suggesting that environmental variance can modify the relative fitness. Conversely, the frequency was suppressed among SI populations (0,2%). Because SI hermaphrodites are free from inbreeding, AD plants would not benefit from inbreeding avoidance and would find it difficult to invade a SI population. [source] Not by Twins Alone: Using the Extended Family Design to Investigate Genetic Influence on Political BeliefsAMERICAN JOURNAL OF POLITICAL SCIENCE, Issue 3 2010Peter K. Hatemi Variance components estimates of political and social attitudes suggest a substantial level of genetic influence, but the results have been challenged because they rely on data from twins only. In this analysis, we include responses from parents and nontwin full siblings of twins, account for measurement error by using a panel design, and estimate genetic and environmental variance by maximum-likelihood structural equation modeling. By doing so, we address the central concerns of critics, including that the twin-only design offers no verification of either the equal environments or random mating assumptions. Moving beyond the twin-only design leads to the conclusion that for most political and social attitudes, genetic influences account for an even greater proportion of individual differences than reported by studies using more limited data and more elementary estimation techniques. These findings make it increasingly difficult to deny that,however indirectly,genetics plays a role in the formation of political and social attitudes. [source] Genetic and environmental influences on serum lipids and the effects of puberty: a Chinese twin studyACTA PAEDIATRICA, Issue 6 2009Tian-Jiao Chen Abstract Aim: To study the contribution of genes and environment on the variation of serum lipids and the effects of puberty. Methods: In total, 314 same-sex twin pairs aged 5,18 years were studied. Puberty was marked physiologically by spermarche/menarche, and model fitting was used to analyse the genetic and environmental variance and its difference before and after puberty. Results: Lipid levels were different before and after puberty. The genetic factor had an important influence on lipid levels; the heritability estimates of total cholesterol (TC), high-density lipoprotein (HDL), low-density lipoprotein (LDL), lipoprotein(a) (Lp(a)) and apolipoprotein E (ApoE) were between 49 and 86%. The total phenotypic variances of TC, HDL, LDL, Lp(a) and ApoE decreased after puberty, mainly as a result of decrease of genetic variance, even though the common environmental variance for HDL, Lp(a) and ApoE increased. Conclusion: Genes and the environment have different effects on the levels of different lipids. The shared environmental effects on lipids are very important in children. The role of puberty on lipids deserves future study. [source] Parenting and Child Behavioral Adjustment in Early Childhood: A Quantitative Genetic Approach to Studying Family ProcessesCHILD DEVELOPMENT, Issue 2 2000Kirby Deater-Deckard The aim of this study was to examine environmental and gene , environment processes linking parenting (i.e., affect, control, responsiveness) and preschool children's behavioral adjustment difficulties (e.g., noncompliance, conduct problems) by using bivariate genetic analyses of parents' and observers' ratings. The sample included 120 identical and same-sex fraternal twin pairs (M age = 43 months). Data sources included in-home observations, interviews, and parents' reports. Observers' ratings of children's difficult behaviors included shared and nonshared environmental variance. In contrast, parents' ratings of children's conduct problems showed genetic and nonshared environmental variance. Observer-rated maternal behavior included shared and nonshared environmental variance, although maternal responsiveness also included child genetic variance. Parent self-reported negative and positive affect included shared and nonshared environment as well as child genetic variance. There was no evidence for gene , environment interaction or dominance. Higher levels of difficult behavior and conduct problems covaried with higher levels of maternal negative affect and control and lower levels of maternal positive affect and control. Shared environmental mediation of these correlations was found for observations, whereas genetic and nonshared environmental mediation was found for parents' ratings. In general, estimates of shared environmental variance and mediation were greatest for observational data, and estimates of child genetic variance and mediation were greatest for parent-rated data. The implications of this pattern of findings for genetic research on family processes are discussed. [source] THE PHENOTYPIC VARIANCE WITHIN PLASTIC TRAITS UNDER MIGRATION-MUTATION-SELECTION BALANCEEVOLUTION, Issue 6 2006Xu-Sheng Zhang Abstract How phenotypic variances of quantitative traits are influenced by the heterogeneity in environment is an important problem in evolutionary biology. In this study, both genetic and environmental variances in a plastic trait under migration-mutation-stabilizing selection are investigated. For this, a linear reaction norm is used to approximate the mapping from genotype to phenotype, and a population of clonal inheritance is assumed to live in a habitat consisting of many patches in which environmental conditions vary among patches and generations. The life cycle is assumed to be selection-reproduction-mutation-migration. Analysis shows that phenotypic plasticity is adaptive if correlations between the optimal phenotype and environment have become established in both space and/or time, and it is thus possible to maintain environmental variance (VE) in the plastic trait. Under the special situation of no mutation but maximum migration such that separate patches form an effective single-site habitat, the genotype that maximizes the geometric mean fitness will come to fixation and thus genetic variance (VG) cannot be maintained. With mutation and/or restricted migration, VG can be maintained and it increases with mutation rate but decreases with migration rate; whereas VE is little affected by them. Temporal variation in environmental quality increases VG while its spatial variance decreases VG. Variation in environmental conditions may decrease the environmental variance in the plastic trait. [source] QUANTITATIVE GENETICS OF SEXUAL PLASTICITY: THE ENVIRONMENTAL THRESHOLD MODEL AND GENOTYPE-BY-ENVIRONMENT INTERACTION FOR PHALLUS DEVELOPMENT IN THE SNAIL BULINUS TRUNCATUSEVOLUTION, Issue 5 2000Marie-France Ostrowski Abstract Sexual polymorphisms are model systems for analyzing the evolution of reproductive strategies. However, their plasticity and other binary traits have rarely been studied, with respect to environmental variables. A possible reason is that, although threshold models offer an adequate quantitative genetics framework for binary traits in a single environment, analyzing their plasticity requires more refined empirical and theoretical approaches. The statistical framework proposed here, based on the environmental threshold model (ETM), should partially fill this gap. This methodology is applied to an empirical dataset on a plastic sexual polymorphism, aphally, in the snail Bulinus truncatus. Aphally is characterized by the co-occurrence of regular hermaphrodites (euphallics) together with hermaphrodites deprived of the male copulatory organ (aphallics). Reaction norms were determined for 40 inbred lines, distributed at three temperatures, in a first experiment. A second experiment allowed us to rule out maternal effects. We confirmed the existence of high broad-sense heritabilities as well as a positive effect of high temperatures on aphally. However a significant genotype-by-environment interaction was detected for the first time, suggesting that sexual plasticity itself can respond to selection. A nested series of four ETM-like models was developed for estimating genetical effects on both mean aphally rate and plasticity. These models were tested using a maximum-likelihood procedure and fitted to aphally data. Although no perfect fit of models to data was observed, the refined versions of ETM models conveniently reduce the analysis of complex reaction norms of binary traits into standard quantitative genetics parameters, such as genetic values and environmental variances. [source] Parent-of-origin, imprinting, mitochondrial, and X-linked effects in traits related to alcohol dependence: Presentation Group 18 of Genetic Analysis Workshop 14GENETIC EPIDEMIOLOGY, Issue S1 2005Konstantin Strauch Abstract The participants of Presentation Group 18 of Genetic Analysis Workshop 14 analyzed the Collaborative Study on the Genetics of Alcoholism data set to investigate sex-specific effects for phenotypes related to alcohol dependence. In particular, the participants looked at imprinting (which is also known as parent-of-origin effect), differences between recombination fractions for the two sexes, and mitochondrial and X-chromosomal effects. Five of the seven groups employed newly developed or existing methods that take imprinting into account when testing for linkage, or test for imprinting itself. Single-marker and multipoint analyses were performed for microsatellite as well as single-nucleotide polymorphism markers, and several groups used a sex-specific genetic map in addition to a sex-averaged map. Evidence for paternal imprinting (i.e., maternal expression) was consistently obtained by at least two groups at genetic regions on chromosomes 10, 12, and 21 that possibly harbor genes responsible for alcoholism. Evidence for maternal imprinting (which is equivalent to paternal expression) was consistently found at a locus on chromosome 11. Two groups applied extensions of variance components analysis that model a mitochondrial or X-chromosomal effect to latent class variables and electrophysiological traits employed in the diagnosis of alcoholism. The analysis, without using genetic markers, revealed mitochondrial or X-chromosomal effects for several of these traits. Accounting for sex-specific environmental variances appeared to be crucial for the identification of an X-chromosomal factor. In linkage analysis using marker data, modeling a mitochondrial variance component increased the linkage signals obtained for autosomal loci. Genet. Epidemiol. 29(Suppl. 1):S125,S132, 2005. © 2005 Wiley-Liss, Inc. [source] | ||||||||||||||||