Age-specific Reproductive Effort Research Articles

Artificial selection for increased dispersal results in lower fitness.

Dispersal often covaries with other traits, and this covariation was shown to have a genetic basis. Here, we wanted to explore to what extent genetic constraints and correlational selection can explain patterns of covariation between dispersal and key life-history traits-lifespan and reproduction. A prediction from the fitness-associated dispersal hypothesis was that lower genetic quality is associated with higher dispersal propensity as driven by the benefits of genetic mixing. We wanted to contrast it with a prediction from a different model that individuals putting more emphasis on current rather than future reproduction disperse more, as they are expected to be more risk-prone and exploratory. However, if dispersal has inherent costs, this will also result in a negative genetic correlation between higher rates of dispersal and some aspects of performance. To explore this issue, we used the dioecious nematode Caenorhabditis remanei and selected for increased and decreased dispersal propensity for 10 generations, followed by five generations of relaxed selection. Dispersal propensity responded to selection, and females from high-dispersal lines dispersed more than females from low-dispersal lines. Females selected for increased dispersal propensity produced fewer offspring and were more likely to die from matricide, which is associated with a low physiological condition in Caenorhabditis nematodes. There was no evidence for differences in age-specific reproductive effort between high- and low-dispersal females. Rather, reproductive output of high-dispersal females was consistently reduced. We argue that our data provide support for the fitness-associated dispersal hypothesis.

Intergenerational effects on offspring telomere length: interactions among maternal age, stress exposure and offspring sex.

Offspring produced by older parents often have reduced longevity, termed the Lansing effect. Because adults usually have similar-aged mates, it is difficult to separate effects of maternal and paternal age, and environmental circumstances are also likely to influence offspring outcomes. The mechanisms underlying the Lansing effect are poorly understood. Variation in telomere length and loss, particularly in early life, is linked to longevity in many vertebrates, and therefore changes in offspring telomere dynamics could be very important in this context. We examined the effect of maternal age and environment on offspring telomere length in zebra finches. We kept mothers under either control (ad libitum food) or more challenging (unpredictable food) circumstances and experimentally minimized paternal age and mate choice effects. Irrespective of the maternal environment, there was a substantial negative effect of maternal age on offspring telomere length, evident in longitudinal and cross-sectional comparisons (average of 39% shorter). Furthermore, in young mothers, sons reared by challenged mothers had significantly shorter telomere lengths than sons reared by control mothers. This effect disappeared when the mothers were old, and was absent in daughters. These findings highlight the importance of telomere dynamics as inter-generational mediators of the evolutionary processes determining optimal age-specific reproductive effort and sex allocation.

Dispersal as a source of variation in age-specific reproductive strategies in a wild population of lizards.

Dispersal syndromes describe the patterns of covariation of morphological, behavioural, and life-history traits associated with dispersal. Studying dispersal syndromes is critical to understanding the demographic and genetic consequences of movements. Among studies describing the association of life-history traits with dispersal, there is anecdotal evidence suggesting that dispersal syndromes can vary with age. Recent theory also suggests that dispersive and philopatric individuals might have different age-specific reproductive efforts. In a wild population of the common lizard (Zootoca vivipara), we investigated whether dispersive and philopatric individuals have different age-specific reproductive effort, survival, offspring body condition, and offspring sex ratio. Consistent with theoretical predictions, we found that young dispersive females have a higher reproductive effort than young philopatric females. Our results also suggest that the early high investment in reproduction of dispersive females trades-off with an earlier onset of senescence than in philopatric females. We further found that young dispersive females produce smaller offspring in lower body condition than do young philopatric females. Overall, our results provide empirical evidence that dispersive and philopatric individuals have different age-specific life-history traits.

Optimal Life-History Strategy Differs between Philopatric and Dispersing Individuals in a Metapopulation

Abundant empirical evidence for dispersal syndromes contrasts with the rarity of theoretical predictions about the evolution of life-history divergence between dispersing and philopatric individuals. We use an evolutionary model to predict optimal differences in age-specific reproductive effort between dispersing and philopatric individuals inhabiting the same metapopulation. In our model, only young individuals disperse, and their lifelong reproductive decisions are potentially affected by this initial event. Juvenile survival declines as density of adults and other juveniles increases. We assume a trade-off between reproduction and survival, so that different patterns of age-specific reproductive effort lead to different patterns of aging. We find that young immigrant mothers should allocate more resources to reproduction than young philopatric mothers, but these life-history differences vanish as immigrant and philopatric individuals get older. However, whether the higher early reproductive effort of immigrants results in higher fecundity depends on the postimmigration cost on fecundity. Dispersing individuals have consequently a shorter life span. Ultimately, these life-history differences are due to the fact that young dispersing individuals most often live in recently founded populations, where competition is relaxed and juvenile survival higher, favoring larger investment in offspring production at the expense of survival.

Optimal life‐history schedule in a metapopulation with juvenile dispersal

Previous models have predicted that when mortality increases with age, older individuals should invest more of their resources in reproduction and produce less dispersive offspring, as both their future reproductive value and their prospect of competing with their own sib decline. Those models assumed stable population sizes. We here study for the first time the evolution of age-specific reproductive effort and of age-specific offspring dispersal rate in a metapopulation with extinction-recolonization dynamics and juvenile dispersal. Our model explores the evolutionary consequences of disequilibrium in the age structure of individuals in local populations, generated by disturbances. Life-history decisions are then shaped both by changes with age in individual performances, and by changes in ecological conditions, as young and old individuals do not live on average in the same environments. Lower juvenile dispersal favours the evolution of higher reproductive effort in young adults in a metapopulation with extinction-recolonization compared with a well-mixed population. Contrary to previous predictions for stable structured populations, we find that offspring dispersal should generally increase with maternal age. This is because young individuals, who are overrepresented in recently colonized populations, should allocate more to reproduction and less to dispersal as a strategy to exploit abundant recruitment opportunities in such populations.

Age-independent and age-dependent decreases in reproduction of females

The terminal allocation and senescence hypotheses make opposite predictions about how age-specific reproductive effort should vary during old age. There is empirical support for both hypotheses, although reports on senescence are more numerous. Individual heterogeneity and selective mortality, however, decrease our ability to measure how reproductive effort varies during late life. The damage accumulation model proposes that terminal allocation and senescence could be partly age-independent. Using a reverse-age approach, we analysed an unusually complete record of annual reproductive success for 90 bighorn ewes that died between 7 and 18years of age. We estimated age-specific and age-independent variation of reproductive effort in late-life. Reproductive effort decreased in the two last reproductions, independently of age at death. Fecundity also decreased in the last 2years of life, with a steeper decline for older individuals. Our study reveals that reproductive senescence includes both age-dependent and age-independent components.

Terminal reproductive effort in a marsupial

Life-history theory predicts that as organisms approach the end of their life, they should increase their reproductive effort (RE). However, studies on mammals often find that measures of RE do not vary with maternal age. This might be because offspring have some control over energy transfer which may constrain adaptive variation in RE by mothers, particularly in eutherian mammals where placental function is primarily controlled by offspring. However, in marsupials, energy transfer is primarily by lactation and under maternal control, leaving marsupial mothers free to vary RE. Here, we provide the first analysis, to our knowledge, of age-specific RE in a marsupial, the common brushtail possum. RE, measured as the proportion of maternal mass lost during lactation, was strongly correlated with offspring mass as a yearling. Older females had higher RE, gave birth earlier in the season and were more likely to produce two offspring in a year. Females with high RE in one year were lighter at the beginning of the next breeding season. These results provide the clearest support yet for terminal RE in a mammal.

AGE-SPECIFIC REPRODUCTIVE SUCCESS: EVIDENCE FOR THE SELECTION HYPOTHESIS

Age-specific reproductive success has been demonstrated in many species. Three hypotheses have been raised to explain this general phenomenon: the experience hypothesis based on age-specific reproductive experience, the effort hypothesis based on age-specific reproductive effort, and the selection hypothesis based on progressive disappearance of phenotypes due to variation in individual productivity and survival. We used data from a long-term study of Leach's storm-petrels (Oceanodroma leucorhoa) to present a single test of mutually exclusive predictions about the relationship between early breeding success and longevity. There should be no correlation between early breeding success and longevity under the experience hypothesis, a negative correlation under the effort hypothesis, and a positive correlation under the selection hypothesis. We found a significant (P < 0.0001) positive relationship between success in the first two breeding attempts and longevity in this population of long-lived seabirds, strongly suggesting that low-productivity parents were also less likely to survive early breeding. These data provide some of the strongest support to date for the selection hypothesis.

Age-Specific Reproduction by Female Laughing Gulls (Larus Atricilla)

Abstract The age at which female gulls first reproduce is poorly documented. We examined plumage and reproductive organs of Laughing Gulls (Larus atricilla) collected from May–August 2000–2001 at John F. Kennedy International Airport, New York, to determine age-specific reproductive effort. Each gull was classified as one year old (hatched in previous year), two years old, or ≥3 years old on the basis of color patterns of the hood and tail feathers and fifth primary flight feather. For females, each ovary was examined to determine if post-ovulatory follicles were present. In 2000 and 2001, the first gulls with postovulatory follicles were recorded on 15 and 18 May, respectively. Overall, 54% of the 211 two-year-old female Laughing Gulls collected during June–August showed evidence of egg laying compared to 88% of the 320 gulls ≥3 years old. None of the 50 one-year-old females examined showed evidence of egg laying. Although a lower proportion of two-year-old females laid eggs compared to older gulls, we found no difference (P ≥ 0.06) in mean number of postovulatory follicles or in frequency distribution of numbers of postovulatory follicles for the two age classes for those birds that did lay eggs. Within each sex, mean body mass increased (P &lt; 0.05) with age. Mean left testis length of males increased (P &lt; 0.05) with age. Our findings clearly established that two-year-old female Laughing Gulls can contribute significantly to the annual reproductive effort and that some adult (≥3 years old) females did not lay eggs.

AGE-SPECIFIC REPRODUCTION BY FEMALE LAUGHING GULLS (LARUS ATRICILLA)

Abstract The age at which female gulls first reproduce is poorly documented. We examined plumage and reproductive organs of Laughing Gulls (Larus atricilla) collected from May–August 2000–2001 at John F. Kennedy International Airport, New York, to determine age-specific reproductive effort. Each gull was classified as one year old (hatched in previous year), two years old, or ≥3 years old on the basis of color patterns of the hood and tail feathers and fifth primary flight feather. For females, each ovary was examined to determine if post-ovulatory follicles were present. In 2000 and 2001, the first gulls with postovulatory follicles were recorded on 15 and 18 May, respectively. Overall, 54% of the 211 two-year-old female Laughing Gulls collected during June–August showed evidence of egg laying compared to 88% of the 320 gulls ≥3 years old. None of the 50 one-year-old females examined showed evidence of egg laying. Although a lower proportion of two-year-old females laid eggs compared to older gulls, we f...

Interactions of environmental temperature with photoperiod in determining age at maturity in a semelparous polychaete Nereis ( neanthes) virens sars

1. 1. Larger members of the Polychacta exhibit two contrasting life cycles: semelparous in the Nereidae, iteroparous in most others. 2. 2. In semelparous forms environmental interaction determines age at reproduction and fecundity in the single spawning event whereas in iteroparous forms such interaction influences the variable age specific reproductive effort. 3. 3. Development of aquaculture has created conditions where organisms are grown under conditions of optimum temperature for growth and unlimited food. 4. 4. We present data on the life history responses (reaction norms) of the semelparous Nereis virens in which age at death in natural populations varies between 3 to 8+ years. 5. 5. In Nereis virens minimum life span (= generation time) in culture is one year but the lifespan remains modular 12 months without manipulation of photoperiod. 6. 6. Environmental temperature plays two roles: i) in conjunction with energy availability to determine “age at first/only reproduction” and secondly as an element (with photoperiod) in the control of gametogenic processes imposing seasonality on the life cycle. 7. 7. The observations suggest that long generation time in natural populations of N. virens is associated with reduced growth rate and that low growth rate is associated with reproduction at a larger size.

Regulating Reproductive Effort in a Changing Environment

Using the ratio of effective reproduction to survival rate, with time scaled in units of time till independence, as an index to age specific reproductive effort, we ask how optimal reproductive effort should vary when environmental conditions change. With an idealized portrayal of the effects of environmental change introduced to a fitness set analysis of the trade-off between reproduction and survival, we find that the optimal reproductive effort is indifferent to environmental change. Deviations from this null case are obtained in a more general model, where we find that a pattern of increasing reproductive effort with environmental amelioration and decreasing reproductive effort with environmental deterioration is predicted when older breeding age classes are less affected by environmental change that are younger age classes, or when the potential adult survival rates are less affected by environmental change than are the potential survival rates of dependent young or the potential natality rates. Where the converse of these conditions obtains, the reverse pattern of change of reproductive effort will be favored. The assumptions of the null-case model provide precise definitions of the threshold conditions at which the pattern of reproductive effort will switch from one type to the other. The circumstances under which regulation of reproductive effort is predicted to be expressed as an increase in reproductive effort in more favorable times and a decrease in less favorable times are commonly met, especially in the life histories of many long-lived vertebrates. Thus the analysis of optimal life histories offers a competing explanation for some patterns of reproductive behavior that are otherwise described as social adaptations that evolved in response to the selective advantage of population regulation.