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Tuljapurkar, S.

Publications and source records attributed to Tuljapurkar, S..

4 recordsLinked to original sources

Demographic determinants of biometric heritability

The response of quantitative characters to selection depends on their transmission from parents to offspring. A common estimate of this transmission is the biometric heritability defined as the slope of the regression of offspring phenotype on same-aged mid-parent phenotype (i.e. the ratio of the phenotypic parent-offspring covariance over the parental phenotypic variance). This slope is often interpreted as the percentage of phenotypic variation due to additive genetic effects after accounting for confounding factors such as environment, litter or parental effects. However, researchers seldom account for the possible influence of selection on this estimate. Here we study the effect on biometric heritability of fertility and viability selection, as well as phenotype ontogeny (growth) and inheritance from parents to offspring. We present exact formulas for the elasticities of biometric heritability in age-phenotype-structured integral projection models (IPMs), and illustrate these for two iteroparous long-lived species. We find that both viability and fertility selection can strongly affect heritability, mediated by growth and inheritance. Generally, demographic processes that result in parents reproducing at large phenotypes, regardless of their own birth phenotype, decrease heritability. Analysed at equilibrium, our models imply that a heritable character can show no response to selection, if parental phenotypes affect offspring phenotypes and if phenotypes develop with age. Our results further highlight the importance of accounting for demographic processes when estimating heritability.

ecology

An Advancing Front of Old Age Human Survival

Old age mortality decline has driven recent increases in lifespans, but there is no agreement about trends in the age-pattern of old deaths. Some hypotheses argue that old-age deaths should have become compressed at high ages, others that old-age deaths should have become more dispersed with age, and yet others are consistent with little change in dispersion. However, direct analyses of old-age deaths presents unusual challenges: death rates at the oldest ages are always noisy; published life tables must assume an asymptotic age pattern of deaths; and the definition of \"old age\" changes as lives lengthen. Here we use robust percentile-based methods to overcome these challenges and show, for 5 decades in 20 developed countries, that old-age survival follows an advancing front, like a traveling wave. The front lies between the 25th and 90th percentiles of old-age deaths, advancing with nearly constant long-term shape but annual fluctuations in speed. The existence of this front leads to several predictions that we verify, e.g., that advances in life expectancy at age 65 are highly correlated with the advance of the 25th percentile, but not with distances between higher percentiles. Our unexpected result has implications for biological hypotheses about human aging, and for future mortality change.

epidemiology

Quantifying genetic, environmental and individual stochastic variability in Plantago lanceolata

Predicting ecological and evolutionary population dynamics requires understanding how genetic and environmental parameters influence variation in survival and reproduction among individuals. However such a focus often neglects the stochastic events that individuals experience throughout their lives that also influence survival and reproduction. With an illustrative example, we quantify and illustrate the influence of such non-selective demographic variability on population dynamics using size-structured matrix models of an experimental population of Plantago lanceolata. Our analysis shows that variation in survival and reproduction among individuals explained by environment, genes, and their interaction was modest compared to the stochastic variation in lifespan and reproduction. We illustrate how expectations on population growth, based on expected lifetime reproduction and generation time, can be misleading when variance in reproduction among individuals of the same genotype (full sibs) was large. Such large within genotype variance can lower population growth, fitness. Our results accompany recent investigations that call for more focus on stochastic variation in survival and reproduction, rather than dismissal of this variation as uninformative noise.

evolutionary biology

Drivers of diversity in individual life courses: Sensitivity of the population entropy of a Markov chain

Individuals differ in their life courses, but how this diversity is generated, how it has evolved and how maintained is less understood. However, this understanding is crucial to comprehend evolutionary and ecological population dynamics. In structured populations, individual life courses represent sequences of stages that end in death. These sequences can be described by a Markov chain and individuals diversify over the course of their lives by transitioning through diverse discrete stages. The rate at which stage sequences diversify with age can be quantified by the population entropy of a Markov chain. Here, we derive sensitivities of the population entropy of a Markov chain to identify which stage transitions generate--or contribute--most to diversification in stage sequences, i.e. life courses. We then use these sensitivities to reveal potential selective forces on the dynamics of life courses. To do so we correlated the sensitivity of each matrix element (stage transition) with respect to the population entropy, to its sensitivity with respect to fitness {lambda}, the population growth rate. Positive correlation between the two sensitivities would suggest that the stage transitions that selection has acted most strongly on (sensitivities with respect to {lambda}) are also those that contributed most to the diversification of life courses. Using an illustrative example on a seabird population, the Thick-billed Murres on Coats Island, that is structured by reproductive stages, we show that the most influential stage transitions for diversification of life courses are not correlated with the most influential transitions for population growth. Our finding suggests that observed diversification in life courses is neutral rather than adaptive. We are at an early stage of understanding how individual level dynamics shape ecological and evolutionary dynamics, and many discoveries await.

evolutionary biology