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Delayed Reproduction (delayed + reproduction)
Selected AbstractsPhenotypic Plasticity of Life History Characteristics: Quantitative Analysis of Delayed Reproduction of Green Foxtail (Setaria viridis) in the Songnen Plain of ChinaJOURNAL OF INTEGRATIVE PLANT BIOLOGY, Issue 6 2008Hai-Yan Li Abstract Green foxtail (Setaria viridis L.) is a common weed species in temperate regions. Research on the effect of delayed reproduction on the phenotypic plasticity and regularity of the vegetative and reproductive growth is of vital significance for understanding population regulation and control of the weed in the growing season. Green foxtail seeds were sown every 10 days from 25 June to 24 August of 2004. The growth and production metrics were measured via harvesting tufts and statistical analysis was carried out. The results showed that the reproductive tillers, seed number, seed biomass and one thousand-seed weight of plants at the first sowing (25 June) approximately increased 28.8, 7 827.0, 1 104.0 and 12.3 times compared with that at the last sowing (24 August), respectively. Total tillers, reproductive tillers and height increased linearly as the reproductive period delayed, however, biomass increased exponentially. Quadratic equations best explained the relationships between the delayed reproductive period and seed number, inflorescence length, one thousand-seed weight, seed biomass. Based on the quantity and quality of seed production, weeding young seedlings emerging before July can be the most effective weed-control strategy in the Songnen Plain. [source] From organisms to populations: Modeling aquatic toxicity data across two levels of biological organizationENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 2 2006Sandy Raimondo Abstract A critical step in estimating the ecological effects of a toxicant is extrapolating organism-level response data across higher levels of biological organization. In the present study, the organism-to-population link is made for the mysid, Americamysis bahia, exposed to a range of concentrations of six toxicants. Organism-level responses observed were categorized as no effect, delayed reproduction, reduced overall reproduction, or both reduced overall reproduction and survival. Population multiplication rates of each toxicant concentration were obtained from matrix models developed from organism-level endpoints and placed into the four categories of organism-level responses. Rates within each category were compared with growth rates modeled for control populations. Population multiplication rates were significantly less than control growth rates only for concentrations at which overall reproduction and both reproduction and survival were significantly less than the control values on the organism level. Decomposition analysis of the significant population-level effects identified reduced reproduction as the primary contributor to a reduced population multiplication rate at all sublethal concentrations and most lethal concentrations. Mortality was the primary contributor to reduced population growth rate only when survival was less than 25% of control survival. These results suggest the importance of altered reproduction in population-level risk assessment and emphasizes the need for complete life-cycle test data to make an explicit link between the organism and population levels. [source] Pulsed resources affect the timing of first breeding and lifetime reproductive success of tawny owlsJOURNAL OF ANIMAL ECOLOGY, Issue 2 2010A. Millon Summary 1.,According to life-history theory, environmental variability and costs of reproduction account for the prevalence of delayed reproduction in many taxa. Empirical estimates of the fitness consequences of different ages at first breeding in a variable environment are few however such that the contributions of environmental and individual variability remains poorly known. 2.,Our objectives were to elucidate processes that underpin variation in delayed reproduction and to assess lifetime consequences of the age of first breeding in a site-faithful predator, the tawny owl Strix aluco L. subjected to fluctuating selection linked to cyclical variation in vole density (typically 3-year cycles with low, increasing and decreasing vole densities in successive years). 3.,A multistate capture,recapture model revealed that owl cohorts had strikingly different juvenile survival prospects, with estimates ranging from 0·08 to 0·33 respectively for birds born in Decrease and Increase phases of the vole cycle. This resulted in a highly skewed population structure with >75% of local recruits being reared during Increase years. In contrast, adult survival remained constant throughout a vole cycle. The probability of commencing reproduction was lower at age 1 than at older ages, and especially so for females. From age 2 onwards, pre-breeders had high probabilities of entering the breeding population. 4.,Variation in lifetime reproductive success was driven by the phase of the vole cycle in which female owls started their breeding career (26,47% of variance explained, whether based on the number of local recruits or fledglings), more than by age at first breeding or by conditions experienced at birth. Females who postponed reproduction to breed for the first time at age 3 during an Increase phase, produced more recruits, even when accounting for birds that may have died before reproduction. No such effects were detected for males. 5.,Sex-specific costs of early reproduction may have accounted for females being more prone to delay reproduction. Contrary to expectations from a best-of-a-bad job strategy, early-hatched, hence potentially higher-quality females were more likely to breed at age 1, but then experienced rapidly declining food resources and so seemed caught in a life-history trap set by the multiannual vole cycle. [source] Empirical tests of life-history evolution theory using phylogenetic analysis of plant demographyJOURNAL OF ECOLOGY, Issue 2 2010Jean H. Burns Summary 1. A primary goal of evolutionary ecology is to understand factors selecting for the diversity of life histories. Life-history components, such as time-to-reproduction, adult survivorship and fecundity, might differ among species because of variation in direct and indirect benefits of these life histories in different environments or might have lower-than-expected variability because of phylogenetic constraints. Here, we present a phylogenetic examination of demography and life histories using a data base of 204 terrestrial plant species. 2. Overall, statistical models without phylogeny were preferred to models with phylogeny for vital rates and elasticities, suggesting that they lacked phylogenetic signal and are evolutionarily labile. However, the effect of phylogeny was significant in models including sensitivities, suggesting that sensitivities exhibit greater phylogenetic signal than vital rates or elasticities. 3. Species with a greater age at first reproduction had lower fecundity, consistent with a cost of delayed reproduction, but only in some habitats (e.g. grassland). We found no evidence for an indirect benefit of delayed reproduction via a decrease in variation in fecundity with age to first reproduction. 4. The greater sensitivity and lower variation in survival than in fecundity was consistent with buffering of more important vital rates, as others have also found. This suggests that studies of life-history evolution should include survival, rather than only fecundity, for the majority of species. 5.Synthesis. Demographic matrix models can provide informative tests of life-history theory because of their shared construction and outputs and their widespread use among plant ecologists. Our comparative analysis suggested that there is a cost of delayed reproduction and that more important vital rates exhibit lower variability. The absolute importance of vital rates to population growth rates (sensitivities) exhibited phylogenetic signal, suggesting that a thorough understanding of life-history evolution might require an understanding of the importance of vital rates, not just their means, and the role of phylogenetic history. [source] Are there interactive effects of mate availability and predation risk on life history and defence in a simultaneous hermaphrodite?JOURNAL OF EVOLUTIONARY BIOLOGY, Issue 5 2008J. R. AULD Abstract Encountering mates and avoiding predators are ubiquitous challenges faced by many organisms and they can affect the expression of many traits including growth, timing of maturity and resource allocation to reproduction. However, these two factors are commonly considered in isolation rather than simultaneously. We examined whether predation risk and mate availability interact to affect morphology and life-history traits (including lifetime fecundity) of a hermaphroditic snail (Physa acuta). We found that mate availability reduced juvenile growth rate and final size. Predator cues from crayfish induced delayed reproduction, but there were no reduced fecundity costs associated with predator induction. Although there were interactive effects on longevity, lifetime fecundity was determined by the number of reproductive days. Therefore, our results indicate a resource-allocation trade-off among growth, longevity and reproduction. Future consideration of this interaction will be important for understanding how resource-allocation plasticity affects the integration of defensive, life-history and mating-system traits. [source] Phenotypic Plasticity of Life History Characteristics: Quantitative Analysis of Delayed Reproduction of Green Foxtail (Setaria viridis) in the Songnen Plain of ChinaJOURNAL OF INTEGRATIVE PLANT BIOLOGY, Issue 6 2008Hai-Yan Li Abstract Green foxtail (Setaria viridis L.) is a common weed species in temperate regions. Research on the effect of delayed reproduction on the phenotypic plasticity and regularity of the vegetative and reproductive growth is of vital significance for understanding population regulation and control of the weed in the growing season. Green foxtail seeds were sown every 10 days from 25 June to 24 August of 2004. The growth and production metrics were measured via harvesting tufts and statistical analysis was carried out. The results showed that the reproductive tillers, seed number, seed biomass and one thousand-seed weight of plants at the first sowing (25 June) approximately increased 28.8, 7 827.0, 1 104.0 and 12.3 times compared with that at the last sowing (24 August), respectively. Total tillers, reproductive tillers and height increased linearly as the reproductive period delayed, however, biomass increased exponentially. Quadratic equations best explained the relationships between the delayed reproductive period and seed number, inflorescence length, one thousand-seed weight, seed biomass. Based on the quantity and quality of seed production, weeding young seedlings emerging before July can be the most effective weed-control strategy in the Songnen Plain. [source] Alcohol Dependence and Reproductive Onset: Findings in Two Australian Twin CohortsALCOHOLISM, Issue 11 2008Mary Waldron Background:, Although early alcohol use is a strong predictor of future alcohol problems and adolescent drinking is associated with risky sexual behavior predictive of early childbearing, reproductive dysfunctions associated with delayed childbearing have been reported in adult drinkers. We examine the relationship between lifetime history of alcohol dependence (AD) and timing of first childbirth across reproductive development. Methods:, Data were drawn from two cohorts of Australian twins born between 1893 and 1964 (3634 female and 1880 male twins) and between 1964 and 1971 (3381 female and 2748 male twins). Survival analyses were conducted using Cox proportional hazards regression models predicting age at first childbirth from AD, with sociodemographic characteristics, regular smoking, history of psychopathology, and family and childhood risks included as control variables in adjusted models. Results:, Results suggest alcoholic women in both cohorts show overall delayed reproduction, with little effect of AD on timing of first reproduction in men. Effects of AD are particularly strong for women in the older cohort, where AD is associated with 73% decreased likelihood of first childbirth after age 29 [hazard ratio (HR) = 0.27, 95% CI: 0.10,0.75]. In adjusted models, effects reduce only slightly (HR = 0.29, 95% CI: 0.11,0.80). For women in the young cohort, AD is associated with delayed reproduction after age 24, with 40% decreased likelihood of first childbirth (HR = 0.60, 95% CI: 0.48,0.75). AD remains predictive in adjusted models, but without age interaction (HR = 0.72, 95% CI: 0.62,0.85). Conclusions:, Findings of delayed reproductive onset in alcoholic women are consistent with alcohol-related reproductive dysfunctions, although underlying mechanisms remain largely unknown. To better understand AD differences in reproductive onset, continued research on both biological and psychosocial risks is needed. [source] Assessment of demographic risk factors and management priorities: impacts on juveniles substantially affect population viability of a long-lived seabirdANIMAL CONSERVATION, Issue 2 2010M. E. Finkelstein Abstract Predicting population-level effects from changes in demographic rates of different life stages is critical to prioritize conservation efforts. Demographic modeling and sensitivity analysis in particular, has become a standard tool to evaluate how management actions influence species' survival. Demographic analyses have resulted in the robust generalization that, for long-lived species with delayed reproduction, population growth rates will be most sensitive to changes in survivorship of older-aged individuals. Although useful in guiding management, this simple maxim may limit options for conservation by causing managers to overlook actions that, although possibly not the most effective in terms of increasing a population's growth rate in an ideal world, can nonetheless more feasibly and rapidly slow a population's decline. We examine the population-level benefits of increasing chick survival in a long-lived seabird, the Laysan albatross Phoebastria immutabilis. Specifically, we use a simple deterministic modeling approach to evaluate the impact of chick mortality (from ingestion of lead-based paint) on the population growth rate (,) for Laysan albatross that breed on Sand Island, Midway Atoll (part of the Hawaiian Archipelago). We estimate that up to 7% of chicks on Sand Island fail to fledge as a result of lead poisoning, which will create a 16% reduction in the Laysan albatross population size (,190 000 less birds) at 50 years into the future. We demonstrate how straightforward management actions that increase juvenile survivorship (e.g. removal of lead-based paint) can help slow population declines while efforts are underway to reduce politically and logistically challenging threats to adult survivorship (e.g. mortality from international fisheries bycatch). Our work exemplifies a situation where overgeneralizations about demography can stifle useful conservation actions and highlights the need to consider the population-level benefits from multiple management strategies. [source] Modelling life history strategies with capture,recapture data: Evolutionary demography of the water skink Eulamprus tympanumAUSTRAL ECOLOGY, Issue 4 2001Simon P. Blomberg Abstract Matrix population models, elasticity analysis and loop analysis can potentially provide powerful techniques for the analysis of life histories. Data from a capture,recapture study on a population of southern highland water skinks (Eulamprus tympanum) were used to construct a matrix population model. Errors in elasticities were calculated by using the parametric bootstrap technique. Elasticity and loop analyses were then conducted to identify the life history stages most important to fitness. The same techniques were used to investigate the relative importance of fast versus slow growth, and rapid versus delayed reproduction. Mature water skinks were long-lived, but there was high immature mortality. The most sensitive life history stage was the subadult stage. It is suggested that life history evolution in E. tympanum may be strongly affected by predation, particularly by birds. Because our population declined over the study, slow growth and delayed reproduction were the optimal life history strategies over this period. Although the techniques of evolutionary demography provide a powerful approach for the analysis of life histories, there are formidable logistical obstacles in gathering enough high-quality data for robust estimates of the critical parameters. [source] | ||||||||||