The impact of reproduction on gambian women: Does controlling for phenotypic quality reveal costs of reproduction?

Life history theory predicts that where resources are limited, investment in reproduction will cause a decline in body condition and ultimately may lower survival rates. We investigate the relationship between reproduction and mortality in women in rural Gambia. We use a number of different measures of reproductive investment: the timing of reproduction, intensity of reproduction, and cumulative reproductive investment (parity). Though giving birth is clearly a risk factor for increased mortality, we find limited evidence that the timing, intensity, or cumulative effects of reproduction have a survival cost. Instead, there is some evidence that women who have invested heavily in reproduction have higher survival than women with lower reproductive investment: both high parity and late age at last reproduction are associated with high survival. The only evidence for any cost of reproduction is that women who have given birth to twins (considered a marker of heavy investment in reproduction) have higher mortality rates than other women, after the age of 50 years. A potential confounding factor may be differences in health between women: particularly healthy women may be able to invest substantially in both reproduction and their own survival, leading to the positive correlations between survival and both parity and age at last birth we observe. To control for differences in health between women, we reanalyze the relationship between reproduction and mortality but include variables correlating with health in our models (height, BMI, and hemoglobin). Even when controlling for health, the positive correlation between investment in reproduction and survival remains unchanged.     

Evolutionary perturbations of optimal life histories

Summary An optimal age-structured life history is perturbed by increasing the mortality factors specific to an agek. These can be density dependent (DD) or independent (DI), avoidable or unavoidable. The last two refer to whether their effect on any individual depends or not on how much energy it devotes to defence. Agespecific trade-offs between the allocation of energy to defence and fecundity exist: survival probabilities through each agex, P_x, are concave decreasing functions of the fecundity per unit size at that age,b_x. These are constraints for the optimal life history. The changes induced by perturbation are evaluated by equations that predict whether some extra energy is diverted towards survivorship at the expense of fecundity or vice versa. The model predicts that for DI environments the degree of avoidability of the mortality source perturbed, is a decisive factor for the strategy selected at agek, but not for any other age class. DD environments are more complex since all ages are simultaneously embedded in density effects. The perturbations not only act directly — as in the DI situation — but also indirectly through their effect on equilibrium density,N^*. When any kind of mortality source becomes more intense at agek, N^* always decreases and all ages react in consequence according to the effect of density on each age-specific trade-off. Either coincidental or opposing reactions can be expected from direct and indirect effects. The resultant strategy for any age would be a matter of magnitude comparisons. Some possible general patterns are discussed.     

Lotic meiofaunal community dynamics: colonisation, resilience and persistence in a spatially and temporally heterogeneous environment

1.  The spatial and temporal dynamics of lotic meiofaunal communities were examined with a focus on colonisation, maintenance of populations in lotic environments and persistence of meiofaunal communities.
2.  Lotic meiofaunal colonisation of new habitats may take place via a number of mechanisms and is rapid at both the patch scale (within hours–days) and the drainage basin scale (within 20 years). Successional patterns in lotic meiofaunal communities are evident although data are extremely limited.
3.  Lotic meiofaunal communities appear to be resilient to high flow disturbances. Resilience is moderated by the availability of in-stream refugia and habitat hydrology. Lotic meiofauna may also adopt a 'refuge as habitat' approach to such disturbances.
4.  Lotic cyclopoid copepods possess a common suite of life history characteristics that confers resilience to disturbances. Compared to pelagic planktonic species they have short generation times, many descendants per reproductive cycle and long lifespans. Females in 'source' populations are likely to survive disturbances and so could continuously reproduce over a long period of time producing large numbers of offspring which develop rapidly and recolonise 'sink' areas of the stream.
5.  Persistence of lotic meiofaunal communities is highly variable. Meiofaunal persistence does not increase with increasing proportions of in-stream flow refugia.     

Dimensionless numbers and life history variation in Brown Trout

Summary Dimensionless numbers, made up from components of life history as defined by growth, mortality and maturation, may provide fresh insights into life history evolution. Most studies have previously shown that these numbers are more or less constants within taxa. The variation between taxa may clarify the evolution of different life histories. We examine the variation in three dimensionless numbers using data from 29 populations of Brown TroutSalmo trutta from Norway, and find that the dimensionless numbers are not constants for the Brown Trout populations. We find that the relationship betweenK of the von Bertalanffy growth equation and the mortality rate (M) increased with increasing growth rate. Also, relative length at maturity (L /L _inf) increased with increasing asymptotic length (L _inf). We suggest that more such data should be collected from a large number of species and taxonomic groups, to allow a more detailed assessment of why these dimensionless numbers appear to be constants in some taxa and not in others.     

Demographic and Female Life History Parameters of Free-Ranging Chimpanzees at the Chimpanzee Rehabilitation Project, River Gambia National Park

We analyzed fertility and mortality records for 113 provisioned, free-ranging chimpanzees at the River Gambia National Park, The Gambia. The chimpanzees are rehabilitated orphans released by the Chimpanzee Rehabilitation Project (CRP), and their descendants born in a natural environment. Females experienced their 1st births at an average age of 14.3 yr, with average interbirth intervals of 68 mo. Despite limited provisioning, reproductive parameters in both released and 1st-generation females resembled those of wild chimpanzees and showed seasonal fluctuations. Mortality rates were low compared to those for wild chimpanzees, particularly for infants and juveniles; life expectancy at birth was 23.6 yr for females and 18 yr for males. The results have implications for our understanding of variation in reproductive parameters between captive and wild chimpanzees. We also discuss issues related to chimpanzee conservation and captive rearing.     

DOES INCREASED MORTALITY FAVOR THE EVOLUTION OF MORE RAPID SENESCENCE?

It is widely believed (following the 1957 hypothesis of G. C. Williams) that greater rates of “extrinsic” (age- and condition-independent) mortality favor more rapid senescence. However, a recent analysis of mammalian life tables failed to find a significant correlation between minimum adult mortality rate and the rate of senescence. This article presents a simple theoretical analysis of how extrinsic mortality should affect the rate of senescence (i.e., the rate at which probability of mortality increases with age) under different evolutionary and population dynamical assumptions. If population dynamics are density independent, extrinsic mortality should not alter the senescence rate favored by natural selection. If population growth is density dependent and populations are stable, the effect of extrinsic mortality depends on the age specificity of the density dependence and on whether survival or reproduction (or both) are functions of density. It is possible that higher extrinsic mortality will increase the rate of senescence at all ages, decrease the rate at all ages, or increase it at some ages while decreasing it at others. Williams's hypothesis is most likely to be supported when density dependence acts primarily on fertility and does not differentially decrease the fertilities of older individuals. Patterns contrary to Williams's prediction are possible when density dependence acts primarily on the survival or fertility of later ages or when most variation in mortality rates is due to variation in nonextrinsic mortality.     

Demography and Life Histories of Sympatric Patas Monkeys, <Emphasis Type="Italic">Erythrocebus patas</Emphasis>, and Vervets, <Emphasis Type="Italic">Cercopithecus aethiops</Emphasis>, in Laikipia,Kenya

Mortality patterns are thought to be strong selective forces on life history traits, with high adult mortality and low immature mortality favoring early and rapid reproduction. Patas monkeys (Erythrocebus patas) have the highest potential rates of population increase for their body size of any haplorhine primate because they reproduce both earlier and more often. We report here 10 yr of comparative demographic data on a population of patas monkeys and a sympatric population of vervet monkeys (Cercopithecus aethiops), a closely related species differing in aspects of social system, ecology, and life history. The data reveal that 1) adult female patas monkeys have significantly higher mortality than adult female vervets; 2) infant mortality in patas monkeys is relatively low compared to the norm for mammals because it is not significantly different from that of adult female patas monkeys; and 3) infant mortality is significantly higher than adult female mortality in vervets. For both species, much of the mortality could be attributed to predation. An epidemic illness was also a major contributor to the mortality of adult female patas monkeys whereas chronic exposure to pathogens in a cold and damp microenvironment may have contributed to the mortality of infant vervets. Both populations experienced large fluctuations during the study period. Our results support the prediction from demographic models of life history evolution that high adult mortality relative to immature mortality selects for early maturation.     

Optimal time to patency in parasitic nematodes: host mortality matters

We develop an optimality model based on classical epidemiological models to investigate the optimal time to patency in parasitic nematodes in relation to host mortality and parasite mortality. We found that the optimal time to patency depends on both host longevity and prepatent mortality of nematodes. We tested our models using a comparative analysis of the relationships between nematode time to patency, nematode mortality and host mortality. Although we confirmed the importance of prepatent mortality, we also found a significant positive influence of host mortality. Host mortality rate affects parasite survivorship and life history strategies in the same way that habitat-specific mortality regimes drive the evolution of life histories in free-living organisms.     

Parasitism as a constraint on the rate of life-history evolution

There are a number of ways in which a host can respond in evolutionary time to reductions in survival and reproduction due to a virulent parasite. These include evolving physiological morphological, or behavioural mechanisms of resistance to infection (or to proliferation, once infection has occurred). But a more unexpected tactic is also possible. This is for hosts to reproduce (slightly) sooner when in the presence of a virulent parasite as compared to when the parasite is less virulent or absent. As such, hosts which reproduce younger may be at a selective advantage, since they can both evade parasitism in time and, even when parasitised, can reduce the likely impact of the parasite on survival and reproductive success. We employ a simple mathematical model to propose that parasites and pathogens can act as important agents in the evolution of the timing of reproduction and associated life-history characters (e.g. body size). Once established in a semelparous host population, evolutionary increases in parasite virulence should result in the evolution of shorter lived hosts; whereas the evolution of less virulent forms of the parasite should be accompanied by the evolution of longer lived hosts. We argue that in the presence of a sufficiently virulent parasite the evolution of longer pre-reproductive life-spans should require the previous or concomitant evolution of morphological, behavioural or physiological resistance to parasitic infection and proliferation.