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History Theory (history + theory)
Kinds of History Theory Selected AbstractsThe senescence of Daphnia from risky and safe habitatsECOLOGY LETTERS, Issue 2 2001Dudycha Evaluating life history in an ecological context is critical for understanding the diversity of life histories found in nature. Lifespan and senescence differ greatly among taxa, but their ecological context is not well known. Life history theory proposes that senescence is ultimately caused by a reduction of the effectiveness of natural selection as organisms age. A key prediction is that different levels of extrinsic mortality risk lead to the evolution of different senescence patterns. I quantified both mortality risk and investment in late-life fitness of Daphnia pulex-pulicaria, a common freshwater zooplankter. I found that Daphnia from high-risk pond habitats invest relatively little in late-life fitness, whereas those from low-risk lake habitats invest relatively more in late-life fitness. This suggests that ecological approaches can be useful for understanding senescence variation. [source] Evolution of avian clutch size along latitudinal gradients: do seasonality, nest predation or breeding season length matter?JOURNAL OF EVOLUTIONARY BIOLOGY, Issue 5 2010E. M. GRIEBELER Abstract Birds display a latitudinal gradient in clutch size with smaller clutches in the tropics and larger in the temperate region. Three factors have been proposed to affect this pattern: seasonality of resources (SR), nest predation and length of the breeding season (LBS). Here, we test the importance of these factors by modelling clutch size evolution within bird populations under different environmental settings. We use an individual-based ecogenetic simulation model that combines principles from population ecology and life history theory. Results suggest that increasing SR from the tropics to the poles by itself or in combination with a decreasing predation rate and LBS can generate the latitudinal gradient in clutch size. Annual fecundity increases and annual adult survival rate decreases from the tropics to the poles. We further show that the annual number of breeding attempts that (together with clutch size) determines total annual egg production is an important trait to understand latitudinal patterns in these life history characteristics. Field experiments that manipulate environmental factors have to record effects not only on clutch size, but also on annual number of breeding attempts. We use our model to predict the outcome of such experiments under different environmental settings. [source] The importance of growth and mortality costs in the evolution of the optimal life historyJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 6 2006D. A. ROFF Abstract A central assumption of life history theory is that the evolution of the component traits is determined in part by trade-offs between these traits. Whereas the existence of such trade-offs has been well demonstrated, the relative importance of these remains unclear. In this paper we use optimality theory to test the hypothesis that the trade-off between present and future fecundity induced by the costs of continued growth is a sufficient explanation for the optimal age at first reproduction, ,, and the optimal allocation to reproduction, G, in 38 populations of perch and Arctic char. This hypothesis is rejected for both traits and we conclude that this trade-off, by itself, is an insufficient explanation for the observed values of , and G. Similarly, a fitness function that assumes a mortality cost to reproduction but no growth cost cannot account for the observed values of ,. In contrast, under the assumption that fitness is maximized, the observed life histories can be accounted for by the joint action of trade-offs between growth and reproductive allocation and between mortality and reproductive allocation (Individual Juvenile Mortality model). Although the ability of the growth/mortality model to fit the data does not prove that this is the mechanism driving the evolution of the optimal age at first reproduction and allocation to reproduction, the fit does demonstrate that the hypothesis is consistent with the data and hence cannot at this time be rejected. We also examine two simpler versions of this model, one in which adult mortality is a constant proportion of juvenile mortality [Proportional Juvenile Mortality (PJM) model] and one in which the proportionality is constant within but not necessarily between species [Specific Juvenile Mortality (SSJM) model]. We find that the PJM model is unacceptable but that the SSJM model produces fits suggesting that, within the two species studied, juvenile mortality is proportional to adult mortality but the value differs between the two species. [source] Early onset of reproductive senescence in domestic sheep Ovis ariesOIKOS, Issue 2 2002Atle Mysterud A central theme in life history theory is to determine how reproduction varies with age in iteroparous organisms. Evidence of ageing and senescence, defined as the progressive loss of function accompanied by decreased performance with age, remains poorly documented for large herbivores, in particular as it relates to reproduction. Analyses of body weight of 87,532 domestic sheep lambs demonstrates that onset of reproductive senescence in ewes occurs already at 5 and 6 years of age when measured, respectively, as lamb weight and litter size produced. This provides convincing evidence of early onset of reproductive senescence in this highly domesticated sheep breed. As this is earlier than indicated for other Ovis species as well as for the Soay sheep, an ancient and lightly domesticated sheep, we hypothesize that there may be a cost of selection for large litter size in mammalian herbivores. [source] Partial life cycle analysis: a model for pre-breeding census dataOIKOS, Issue 3 2001Madan K. Oli Matrix population models have become popular tools in research areas as diverse as population dynamics, life history theory, wildlife management, and conservation biology. Two classes of matrix models are commonly used for demographic analysis of age-structured populations: age-structured (Leslie) matrix models, which require age-specific demographic data, and partial life cycle models, which can be parameterized with partial demographic data. Partial life cycle models are easier to parameterize because data needed to estimate parameters for these models are collected much more easily than those needed to estimate age-specific demographic parameters. Partial life cycle models also allow evaluation of the sensitivity of population growth rate to changes in ages at first and last reproduction, which cannot be done with age-structured models. Timing of censuses relative to the birth-pulse is an important consideration in discrete-time population models but most existing partial life cycle models do not address this issue, nor do they allow fractional values of variables such as ages at first and last reproduction. Here, we fully develop a partial life cycle model appropriate for situations in which demographic data are collected immediately before the birth-pulse (pre-breeding census). Our pre-breeding census partial life cycle model can be fully parameterized with five variables (age at maturity, age at last reproduction, juvenile survival rate, adult survival rate, and fertility), and it has some important applications even when age-specific demographic data are available (e.g., perturbation analysis involving ages at first and last reproduction). We have extended the model to allow non-integer values of ages at first and last reproduction, derived formulae for sensitivity analyses, and presented methods for estimating parameters for our pre-breeding census partial life cycle model. We applied the age-structured Leslie matrix model and our pre-breeding census partial life cycle model to demographic data for several species of mammals. Our results suggest that dynamical properties of the age-structured model are generally retained in our partial life cycle model, and that our pre-breeding census partial life cycle model is an excellent proxy for the age-structured Leslie matrix model. [source] Reproductive development and parental investment during pregnancy: Moderating influence of mother's early environmentAMERICAN JOURNAL OF HUMAN BIOLOGY, Issue 2 2010David A. Coall The association between a woman's age at menarche and the birth weight of her children is highly variable across human populations. Life history theory proposes that a woman's early environment may moderate this association and thus account for some of the variation between populations. According to one life history theory model, for individuals who develop in a childhood environment of high local mortality rates (experienced subjectively as psychosocial stress), it can be adaptive to mature earlier, have more offspring during their reproductive lifetime, and reduce investment in each offspring. In an environment of low psychosocial stress, however, it may be adaptive to mature later, have fewer offspring, and invest more in each. In this study, birth weight and proportionate birth weight (neonate's birth weight as a percentage of its mother's prepregnancy weight) were used as measures of parental investment during pregnancy. In a sample of 580 first-time mothers, we tested the hypothesis that the psychosocial stress experienced as a child would moderate the association between age at menarche and investment during pregnancy. We found that earlier menarche in those women who experienced stressful life events before 15 years of age was associated with a lower birth weight and proportionate birth weight. Conversely, in those who reported no childhood stressors, earlier menarche was associated with increased birth weight and proportionate birth weight. Our data suggest that the moderating influence of the childhood psychosocial environment on the association between age at menarche and parental investment throughout gestation operates in a dose-dependent manner. Am. J. Hum. Biol., 2010. © 2009 Wiley-Liss, Inc. [source] Endocrine mechanisms of primate life history trade-offs: Growth and reproductive maturation in vervet monkeysAMERICAN JOURNAL OF HUMAN BIOLOGY, Issue 6 2009Patricia L. Whitten Life history theory predicts that the timing of maturation will result from a trade-off between growth and the age of first reproduction. This trade-off and its mechanisms of action are still poorly understood in many species and have not been well studied at the individual level. This study examined hypothesized trade-offs between growth and reproductive maturation in wild populations of vervet monkeys (Cercopithecus aethiops) from Kenya, East Africa. Individuals were sampled from four populations in widely separated sites differing in temperature, altitude, and rainfall. Biological samples and morphometric measures were collected from 50 adult males, 83 adult females, and 225 juveniles. Gonadal steroids and leptin levels were analyzed by radioimmunoassay of sera from 136 juvenile males and 90 juvenile females. Cross-sectional profiles of morphometric and endocrine data were used to assess the onset and cessation of growth in relation to sexual maturation. Gonadal steroids were used to assess sexual maturation and breeding onset. Leptin was used as an index of nutritional state. Estimates of mortality were derived from population age-structure. Across populations, higher resource productivity and nutrient status were associated with more rapid growth. Shorter growth duration was associated with earlier reproductive onset. These findings provide support for models of trade-offs between the timing of growth completion and reproductive onset, but they are contradicted by the evidence that reproduction precedes the cessation of growth in these populations. The biphasic actions of estradiol provide an alternative model and mechanism for the growth-reproduction trade-off. Am. J. Hum. Biol., 2009. © 2009 Wiley-Liss, Inc. [source] Seasonal and circadian variation in salivary testosterone in rural Bolivian menAMERICAN JOURNAL OF HUMAN BIOLOGY, Issue 6 2009Virginia J. Vitzthum Testosterone (T) plays a key role in the increase and maintenance of muscle mass and bone density in adult men. Life history theory predicts that environmental stress may prompt a reallocation of such investments to those functions critical to survival. We tested this hypothesis in two studies of rural Bolivian adult men by comparing free T levels and circadian rhythms during late winter, which is especially severe, to those in less arduous seasons. For each pair of salivary TAM/TPM samples (collected in a , 12-h period), circadian rhythm was considered classic (CCLASSIC) if TAM > 110%TPM, reverse (CREVERSE) if TPM > 110%TAM, and flat (CFLAT) otherwise. We tested the hypotheses that mean TAM > mean TPM and that mean TLW < mean TOTHER (LW = late winter, OTHER = other seasons). In Study A, of 115 TPM,TAM pairs, 51% = CCLASSIC, 39% = CREVERSE, 10% = CFLAT; in Study B, of 184 TAM,TPM pairs, 55% = CCLASSIC, 33% = CREVERSE, 12% = CFLAT. Based on fitting linear mixed models, in both studies TOTHER-AM > TOTHER-PM (A: P = 0.035, B: P = 0.0005) and TOTHER-AM > TLW-AM (A: P = 0.054, B: P = 0.007); TPM did not vary seasonally, and T diurnality was not significant during late winter. T diurnality varied substantially between days within an individual, between individuals and between seasons, but neither T levels nor diurnality varied with age. These patterns may reflect the seasonally varying but unscheduled, life-long, strenuous physical labor that typifies many non-industrialized economies. These results also suggest that single morning samples may substantially underestimate peak circulating T for an individual and, most importantly, that exogenous signals may moderate diurnality and the trajectory of age-related change in the male gonadal axis. Am. J. Hum. Biol., 2009. © 2009 Wiley-Liss, Inc. [source] Habits of the heart: Life history and the developmental neuroendocrinology of emotionAMERICAN JOURNAL OF HUMAN BIOLOGY, Issue 6 2009Carol M. Worthman The centrality of emotion in cognition and social intelligence as well as its impact on health has intensified investigation into the causes and consequences of individual variation in emotion regulation. Central processing of experience directly informs regulation of endocrine axes, essentially forming a neuro-endocrine continuum integrating information intake, processing, and physiological and behavioral response. Two major elements of life history,resource allocation and niche partitioning,are served by linking cognitive-affective with physiologic and behavioral processes. Scarce cognitive resources (attention, memory, and time) are allocated under guidance from affective co-processing. Affective-cognitive processing, in turn, regulates physiologic activity through neuro-endocrine outflow and thereby orchestrates energetic resource allocation and trade-offs, both acutely and through time. Reciprocally, peripheral activity (e.g., immunologic, metabolic, or energetic markers) influences affective-cognitive processing. By guiding attention, memory, and behavior, affective-cognitive processing also informs individual stances toward, patterns of activity in, and relationships with the world. As such, it mediates processes of niche partitioning that adaptively exploit social and material resources. Developmental behavioral neurobiology has identified multiple factors that influence the ontogeny of emotion regulation to form affective and behavioral styles. Evidence is reviewed documenting roles for genetic, epigenetic, and experiential factors in the development of emotion regulation, social cognition, and behavior with important implications for understanding mechanisms that underlie life history construction and the sources of differential health. Overall, this dynamic arena for research promises to link the biological bases of life history theory with the psychobehavioral phenomena that figure so centrally in quotidian experience and adaptation, particularly, for humans. Am. J. Hum. Biol. 2009. © 2009 Wiley-Liss, Inc. [source] Pooled energy budget and human life historyAMERICAN JOURNAL OF HUMAN BIOLOGY, Issue 4 2009Meredith W. Reiches Human life history contains a series of paradoxes not easily explained by classical life history theory. Although overall reproductive output is higher than in related primates, juvenile growth is slower and age-specific reproductive rates decline faster with age. A simple energetic model would predict that growth and reproductive rates should be positively correlated and that reproductive effort should not decelerate with age. The pattern of negative correlations in humans suggest the presence of trade-offs among peak reproductive rate, childhood growth, and reproductive rate at older ages. To address this puzzle, we propose a synthesis of reproductive ecology and behavioral ecology focused on intra- and inter-somatic energy transfers. This integration includes three concepts: the mother as final common pathway through which energy must pass to result in offspring; a distinction between direct and indirect reproductive effort, proposing the latter as a novel net energy allocation category relative to growth and direct reproductive effort; and a pooled energy budget representing the energetic contributions and withdrawals of all members of a breeding community. Individuals at all reproductive life stages are considered in light of their contributions to the pooled energy budget. Am. J. Hum. Biol., 2009. © 2009 Wiley-Liss, Inc. [source] Early reproductive maturity among Pumé foragers: Implications of a pooled energy model to fast life historiesAMERICAN JOURNAL OF HUMAN BIOLOGY, Issue 4 2009Karen L. Kramer Life history theory places central importance on relationships between ontogeny, reproduction, and mortality. Fast human life histories have been theoretically and empirically associated with high mortality regimes. This relationship, however, poses an unanswered question about energy allocation. In epidemiologically stressful environments, a greater proportion of energy is allocated to immune function. If growth and maintenance are competing energetic expenditures, less energy should be available for growth, and the mechanism to sustain rapid maturation remains unclear. The human pattern of extended juvenile provisioning and resource sharing may provide an important source of variation in energy availability not predicted by tradeoff models that assume independence at weaning. We consider a group of South American foragers to evaluate the effects that pooled energy budgets may have on early reproduction. Despite growing up in an environment with distinct seasonal under-nutrition, harsh epidemiological conditions, and no health care, Pumé girls mature quickly and initiate childbearing in their midteens. Pooled energy budgets compensate for the low productivity of girls not only through direct food transfers but importantly by reducing energy they would otherwise expend in foraging activities to meet metabolic requirements. We suggest that pooled energy budgets affect energy availability at both extrinsic and intrinsic levels. Because energy budgets are pooled, Pumé girls and young women are buffered from environmental downturns and can maximize energy allocated to growth completion and initiate reproduction earlier than a traditional bound-energy model would predict. Am. J. Hum. Biol., 2009. © 2009 Wiley-Liss, Inc. [source] Seasonal modulation of reproductive effort during early pregnancy in humans,AMERICAN JOURNAL OF HUMAN BIOLOGY, Issue 4 2009Virginia J. Vitzthum Life history theory predicts that early pregnancy presents a relatively low cost, uncontested opportunity for a woman to terminate investment in a current reproductive opportunity if a conceptus is of poor quality and/or maternal status or environmental conditions are not propitious for a successful birth. We tested this hypothesis in rural Bolivian women experiencing substantial seasonal variation in workload and food resources. Significant risk factors for early pregnancy loss (EPL) included agropastoralism versus other economic strategies, conception during the most arduous seasons versus other seasons, and increasing maternal age. Anovulation rate (AR) was higher during the most arduous seasons and in older women. Breastfeeding and indicators of social status and living conditions did not significantly influence either risk of EPL or AR. Averaged over the year, anovulation occurred in about 1/4 of the cycles and EPL occurred in about 1/3 of the conceptions. This is the first evidence of seasonality of EPL in a non-industrialized population, and the first to demonstrate a relationship between economic activities and EPL. These findings suggest that both anovulation and EPL are potential mechanisms for modulating reproductive effort; such "failures" may also be nonadaptive consequences of conditions hostile to a successful pregnancy. In either case, variation in EPL risk associated with different subsistence activities can be expected to influence fertility levels and birth seasonality in both contemporary and past human populations. These consequences of variability in the risk of EPL can impact efforts to understand the sources of variation in reproductive success. Am. J. Hum. Biol., 2009. © 2009 Wiley-Liss, Inc. [source] Early life events and their consequences for later disease: A life history and evolutionary perspectiveAMERICAN JOURNAL OF HUMAN BIOLOGY, Issue 1 2007Peter D. Gluckman Biomedical science has little considered the relevance of life history theory and evolutionary and ecological developmental biology to clinical medicine. However, the observations that early life influences can alter later disease risk,the "developmental origins of health and disease" (DOHaD) paradigm,have led to a recognition that these perspectives can inform our understanding of human biology. We propose that the DOHaD phenomenon can be considered as a subset of the broader processes of developmental plasticity by which organisms adapt to their environment during their life course. Such adaptive processes allow genotypic variation to be preserved through transient environmental changes. Cues for plasticity operate particularly during early development; they may affect a single organ or system, but generally they induce integrated adjustments in the mature phenotype, a process underpinned by epigenetic mechanisms and influenced by prediction of the mature environment. In mammals, an adverse intrauterine environment results in an integrated suite of responses, suggesting the involvement of a few key regulatory genes, that resets the developmental trajectory in expectation of poor postnatal conditions. Mismatch between the anticipated and the actual mature environment exposes the organism to risk of adverse consequences,the greater the mismatch, the greater the risk. For humans, prediction is inaccurate for many individuals because of changes in the postnatal environment toward energy-dense nutrition and low energy expenditure, contributing to the epidemic of chronic noncommunicable disease. This view of human disease from the perspectives of life history biology and evolutionary theory offers new approaches to prevention, diagnosis and intervention. Am. J. Hum. Biol. 19:1,19, 2007. © 2006 Wiley-Liss, Inc. © 2006 Wiley-Liss, Inc. [source] Fetal origins of developmental plasticity: Are fetal cues reliable predictors of future nutritional environments?AMERICAN JOURNAL OF HUMAN BIOLOGY, Issue 1 2005Christopher W. Kuzawa Evidence that fetal nutrition triggers permanent adjustments in a wide range of systems and health outcomes is stimulating interest in the evolutionary significance of these responses. This review evaluates the postnatal adaptive significance of fetal developmental plasticity from the perspective of life history theory and evolutionary models of energy partitioning. Birthweight is positively related to multiple metabolically costly postnatal functions, suggesting that the fetus has the capacity to distribute the burden of energy insufficiency when faced with a nutritionally challenging environment. Lowering total requirements may reduce the risk of negative energy balance, which disproportionately impacts functions that are not essential for survival but that are crucial for reproductive success. The long-term benefit of these metabolic adjustments is contingent upon the fetus having access to a cue that is predictive of its future nutritional environment, a problem complicated in a long-lived species by short-term ecologic fluctuations like seasonality. Evidence is reviewed suggesting that the flow of nutrients reaching the fetus provides an integrated signal of nutrition as experienced by recent matrilineal ancestors, which effectively limits the responsiveness to short-term ecologic fluctuations during any given pregnancy. This capacity for fetal nutrition to minimize the growth response to transient ecologic fluctuations is defined here as intergenerational "phenotypic inertia," and is hypothesized to allow the fetus to cut through the "noise" of seasonal or other stochastic influences to read the "signal" of longer-term ecologic trends. As a mode of adaptation, phenotypic inertia may help the organism cope with ecologic trends too gradual to be tracked by conventional developmental plasticity, but too rapid to be tracked by natural selection. From an applied perspective, if a trait like fetal growth is designed to minimize the effects of short-term fluctuations by integrating information across generations, public health interventions may be most effective if focused not on the individual but on the matriline. Am. J. Hum. Biol. 17:5,21, 2005. © 2004 Wiley-Liss, Inc. [source] An evolutionary ecological perspective on demographic transitions: Modeling multiple currenciesAMERICAN JOURNAL OF HUMAN BIOLOGY, Issue 2 2002Bobbi S. Low Life history theory postulates tradeoffs of current versus future reproduction; today women face evolutionarily novel versions of these tradeoffs. Optimal age at first birth is the result of tradeoffs in fertility and mortality; ceteris paribus, early reproduction is advantageous. Yet modern women in developed nations experience relatively late first births; they appear to be trading off socioeconomic status and the paths to raised SES, education and work, against early fertility. Here, [1] using delineating parameter values drawn from data in the literature, we model these tradeoffs to determine how much socioeconomic advantage will compensate for delayed first births and lower lifetime fertility; and [2] we examine the effects of work and education on women's lifetime and age-specific fertility using data from seven cohorts in the Panel Study of Income Dynamics (PSID). Am. J. Hum. Biol. 14:149,167, 2002. © 2002 Wiley-Liss, Inc. [source] The ecology and evolutionary endocrinology of reproduction in the human femaleAMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY, Issue S49 2009Virginia J. Vitzthum Abstract Human reproductive ecology (HRE) is the study of the mechanisms that link variation in reproductive traits with variation in local habitats. Empirical and theoretical contributions from biological anthropology, physiology, and demography have established the foundation necessary for developing a comprehensive understanding, grounded in life history theory (LHT), of temporal, individual, and populational variation in women's reproductive functioning. LHT posits that natural selection leads to the evolution of mechanisms that tend to allocate resources to the competing demands of growth, reproduction, and survival such that fitness is locally maximized. (That is, among alternative allocation patterns exhibited in a population, those having the highest inclusive fitness will become more common over generational time.) Hence, strategic modulation of reproductive effort is potentially adaptive because investment in a new conception may risk one's own survival, future reproductive opportunities, and/or current offspring survival. The hypothalamic-pituitary-ovarian (HPO) axis is the principal neuroendocrine pathway by which the human female modulates reproductive functioning according to the changing conditions in her habitat. Adjustments of reproductive investment in a potential conception are manifested in temporal and individual variation in ovarian cycle length, ovulation, hormone levels, and the probability of conception. Understanding the extent and causes of adaptive and non-adaptive variation in ovarian functioning is fundamental to ascertaining the proximate and remote determinants of human reproductive patterns. In this review I consider what is known and what still needs to be learned of the ecology of women's reproductive biology, beginning with a discussion of the principal explanatory frameworks in HRE and the biometry of ovarian functioning. Turning next to empirical studies, it is evident that marked variation between cycles, women, and populations is the norm rather than an aberration. Other than woman's age, the determinants of these differences are not well characterized, although developmental conditions, dietary practices, genetic variation, and epigenetic mechanisms have all been hypothesized to play some role. It is also evident that the reproductive functioning of women born and living in arduous conditions is not analogous to that of athletes, dieters, or even the lower end of the "normal range" of HPO functioning in wealthier populations. Contrary to the presumption that humans have low fecundity and an inefficient reproductive system, both theory and present evidence suggest that we may actually have very high fecundity and a reproductive system that has evolved to be flexible, ruthlessly efficient and, most importantly, strategic. Yrbk Phys Anthropol 52:95,136, 2009. © 2009 Wiley-Liss, Inc. [source] | ||||||||||