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1.
Heredity (Edinb) ; 117(3): 184-90, 2016 09.
Article in English | MEDLINE | ID: mdl-27381323

ABSTRACT

Maternal reproductive investment can critically influence offspring phenotype, and thus these maternal effects are expected to be under strong natural selection. Knowledge on the extent of heritable variation in the physiological mechanisms underlying maternal effects is however limited. In birds, resource allocation to eggs is a key mechanism for mothers to affect their offspring and different components of the egg may or may not be independently adjusted. We studied the heritability of egg components and their genetic and phenotypic covariation in great tits (Parus major), using captive-bred full siblings of wild origin. Egg mass, testosterone (T) and androstenedione (A4) hormone concentrations showed moderate heritability, in agreement with earlier findings. Interestingly, yolk triiodothyronine hormone (T3), but not its precursor, thyroxine hormone (T4), concentration was heritable. An immune factor, albumen lysozyme, showed moderate heritability, but yolk immunoglobulins (IgY) did not. The genetic correlation estimates were moderate but statistically nonsignificant; a trend for a positive genetic correlation was found between A4 and egg mass, T and lysozyme and IgY and lysozyme, respectively. Interestingly, phenotypic correlations were found only between A4 and T, and T4 and T3, respectively. Given that these egg components are associated with fitness-related traits in the offspring (and mother), and that we show that some components are heritable, it opens the possibility that natural selection may shape the rate and direction of phenotypic change via egg composition.


Subject(s)
Androgens/genetics , Egg Yolk/chemistry , Immunologic Factors/genetics , Inheritance Patterns , Songbirds/genetics , Thyroid Hormones/genetics , Animals , Female , Immunoglobulins/genetics , Models, Genetic , Muramidase/genetics , Phenotype , Selection, Genetic
2.
J Evol Biol ; 27(9): 1849-58, 2014 09.
Article in English | MEDLINE | ID: mdl-24930732

ABSTRACT

Spatial and temporal phenotypic differentiation in mean body size is of commonplace occurrence, but the underlying causes remain often unclear: both genetic differentiation in response to selection (or drift) and environmentally induced plasticity can create similar phenotypic patterns. Studying changes in body mass in Siberian jays (Perisoreus infaustus) over three decades, we discovered that mean body mass declined drastically (ca. 10%) over the first two decades, but increased markedly thereafter back to almost the initial level. Quantitative genetic analyses revealed that although body mass was heritable (h(2) = 0.46), the pronounced temporal decrease in body mass was mainly a product of phenotypic plasticity. However, a concomitant and statistically significant decrease in predicted breeding values suggests a genetic component to this change. The subsequent increase in mean body mass was indicated to be entirely due to plasticity. Selection on body mass was estimated to be too weak to fully account for the observed genetic decline in body mass, but bias in selection differential estimates due to environmental covariance between body mass and fitness is possible. Hence, the observed body mass changes appear to be driven mainly by phenotypic plasticity. Although we were not able to identify the ecological driver of the observed plastic changes, the results highlight the utility of quantitative genetic approaches in disentangling genetic and phenotypic changes in natural populations.


Subject(s)
Body Weight/genetics , Passeriformes/genetics , Animals , Body Size , Climate Change , Female , Finland , Longitudinal Studies , Male , Models, Genetic , Passeriformes/physiology , Phenotype , Quantitative Trait, Heritable , Selection, Genetic
3.
J Evol Biol ; 26(12): 2739-45, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24118141

ABSTRACT

Many organisms advance their seasonal reproduction in response to global warming. In birds, which regress their gonads to a nonfunctional state each winter, these shifts are ultimately constrained by the time required for gonadal development in spring. Gonadal development is photoperiodically controlled and shows limited phenotypic plasticity in relation to environmental factors, such as temperature. Heritable variation in the time required for full gonadal maturation to be completed, based on both onset and speed of development and resulting in seasonally different gonad sizes among individuals, is thus a crucial prerequisite for an adaptive advancement of seasonal reproduction in response to changing temperatures. We measured seasonal gonadal development in climate-controlled aviaries for 144 great tit (Parus major) pairs, which consisted of siblings obtained as whole broods from the wild. We show that the extent of ovarian follicle development (follicle size) in early spring is highly heritable (h(2) = 0.73) in females, but found no heritability of the extent of testis development in males. However, heritability in females decreased as spring advanced, caused by an increase in environmental variance and a decrease in additive genetic variation. This low heritability of the variation in a physiological mechanism underlying reproductive timing at the time of selection may hamper genetic adaptation to climate change, a key insight as this great tit population is currently under directional selection for advanced egg-laying.


Subject(s)
Genitalia/anatomy & histology , Seasons , Songbirds/anatomy & histology , Animals , Female , Male
4.
J Evol Biol ; 26(10): 2147-53, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23837446

ABSTRACT

Avian seasonal timing is a life-history trait with important fitness consequences and which is currently under directional selection due to climate change. To predict micro-evolution in this trait, it is crucial to properly estimate its heritability. Heritabilities are often estimated from pedigreed wild populations. As these are observational data, it leaves the possibility that the resemblance between related individuals is not due to shared genes but to ontogenetic effects; when the environment for the offspring provided by early laying pairs differs from that by late pairs and the laying dates of these offspring when they reproduce themselves is affected by this environment, this may lead to inflated heritability estimates. Using simulation studies, we first tested whether and how much such an early environmental effect can inflate heritability estimates from animal models, and we showed that pedigree structure determines by how much early environmental effects inflate heritability estimates. We then used data from a wild population of great tits (Parus major) to compare laying dates of females born early in the season in first broods and from sisters born much later, in second broods. These birds are raised under very different environmental conditions but have the same genetic background. The laying dates of first and second brood offspring do not differ when they reproduce themselves, clearly showing that ontogenetic effects are very small and hence, family resemblance in timing is due to genes. This finding is essential for the interpretation of the heritabilities reported from wild populations and for predicting micro-evolution in response to climate change.


Subject(s)
Passeriformes/physiology , Reproduction , Seasons , Sexual Behavior, Animal , Animals , Climate Change , Computer Simulation , Nesting Behavior , Passeriformes/genetics
5.
J Evol Biol ; 23(6): 1148-58, 2010 Jun 01.
Article in English | MEDLINE | ID: mdl-20345812

ABSTRACT

The effective population size is a central concept for understanding evolutionary processes in a finite population. We employ Fisher's reproductive value to estimate the ratio of effective to actual population size for an age-structured population with two sexes using random samples of individual vital rates. The population may be subject to environmental stochasticity affecting the vital rates. When the mean sex ratio at birth is known, improved efficiency is obtained by utilizing the records of total number of offspring rather than considering separately female and male offspring. We also show how to incorporate uncertain paternity.


Subject(s)
Demography , Animals , Birds , Female , Fertility , Male , Models, Theoretical , Sex Ratio , Uncertainty
6.
J Evol Biol ; 23(4): 715-23, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20210831

ABSTRACT

Condition, defined as the amount of 'internal resources' an individual can freely allocate, is often assumed to be environmentally determined and to reflect an individual's health and nutritional status. However, an additive genetic component of condition is possible if it 'captures' the genetic variance of many underlying traits as many fitness-related traits appear to do. Yet, the heritability of condition can be low if selection has eroded much of its additive genetic variance, or if the environmental influences are strong. Here, we tested whether feather growth rate - presumably a condition-dependent trait - has a heritable component, and whether variation in feather growth rate is related to variation in fitness. To this end, we utilized data from a long-term population study of Siberian jays (Perisoreus infaustus), and found that feather growth rate, measured as the width of feather growth bars (GB), differed between age-classes and sexes, but was only weakly related to variation in fitness as measured by annual and life-time reproductive success. As revealed by animal model analyses, GB width was significantly heritable (h(2) = 0.10 +/- 0.05), showing that this measure of condition is not solely environmentally determined, but reflects at least partly inherited genetic differences among individuals. Consequently, variation in feather growth rates as assessed with ptilochronological methods can provide information about heritable genetic differences in condition.


Subject(s)
Feathers/growth & development , Songbirds/genetics , Songbirds/physiology , Aging/physiology , Animals , Body Weight , Environment , Female , Male , Reproduction , Sex Characteristics
7.
Mol Ecol ; 17(1): 167-78, 2008 Jan.
Article in English | MEDLINE | ID: mdl-18173499

ABSTRACT

Rapid climate change is likely to impose strong selection pressures on traits important for fitness, and therefore, microevolution in response to climate-mediated selection is potentially an important mechanism mitigating negative consequences of climate change. We reviewed the empirical evidence for recent microevolutionary responses to climate change in longitudinal studies emphasizing the following three perspectives emerging from the published data. First, although signatures of climate change are clearly visible in many ecological processes, similar examples of microevolutionary responses in literature are in fact very rare. Second, the quality of evidence for microevolutionary responses to climate change is far from satisfactory as the documented responses are often - if not typically - based on nongenetic data. We reinforce the view that it is as important to make the distinction between genetic (evolutionary) and phenotypic (includes a nongenetic, plastic component) responses clear, as it is to understand the relative roles of plasticity and genetics in adaptation to climate change. Third, in order to illustrate the difficulties and their potential ubiquity in detection of microevolution in response to natural selection, we reviewed the quantitative genetic studies on microevolutionary responses to natural selection in the context of long-term studies of vertebrates. The available evidence points to the overall conclusion that many responses perceived as adaptations to changing environmental conditions could be environmentally induced plastic responses rather than microevolutionary adaptations. Hence, clear-cut evidence indicating a significant role for evolutionary adaptation to ongoing climate warming is conspicuously scarce.


Subject(s)
Biological Evolution , Climate , Environment , Greenhouse Effect , Phenotype , Selection, Genetic , Vertebrates/genetics , Adaptation, Biological/genetics , Adaptation, Biological/physiology , Animals , Reproduction/genetics
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