The persistence niche: what makes it and what breaks it for two fire-prone plant species

2007 ◽  
Vol 55 (3) ◽  
pp. 273 ◽  
Author(s):  
David A. Keith ◽  
Mark G. Tozer ◽  
Tracey J. Regan ◽  
Helen M. Regan

Persistence niches are expected to favour qualitatively different plant life histories compared with regeneration niches. In fire-prone habitats, for example, resprouting plants may be expected to exploit persistence niches, whereas obligate-seeders by definition exploit regeneration niches. Resprouter life histories should be typified by high rates of survival, which may be offset by relatively low rates of growth and reproduction. This combination of characters is expected to result from trade-offs in resource allocation and because the longevity of individual plants should buffer their populations against the effects of recruitment failure. We asked whether two resprouting perennial shrubs, Epacris barbata Melville and Xanthorrhoea resinifera (Sol. Ex Kite) E.C.Nelson & D.J.Bedford, exhibited the life-history character combinations that are expected for species exploiting a persistence niche. We also investigated how a change in habitat suitability caused by the invasion of a root pathogen may limit the ability of these species to occupy persistence niches. Demographic censuses of several years’ duration in two populations of each species yielded estimates of vital rates that were consistent with the life-history profile expected for a persistence niche. Rates of background survival were high and rates of fire-related mortality were low in both species. As expected, these were associated with low rates of growth and seedling establishment, although rates of seed production and viability were relatively high in both species. The importance of survival was confirmed by stochastic population models, which showed that population viability was more sensitive to decreases in survival of mature plants and increases in fire mortality of established plants than to changes in other vital rates. Seedling growth rates were also relatively important in E. barbata. Populations of both species that had been infected by root rot disease, Phytophthora cinnamomi, had substantially reduced survival rates and, consequently, reduced population viability. These effects were more extreme in E. barbata than in X. resinifera. We conclude that processes that reduce survival, such as disease infection and habitat loss, rather than processes that impede seed production and recruitment mediate the persistence niche. However, we discuss the possibility that this dependency might be mitigated by high fecundity if infrequent conditions that permit large recruitment events have so far eluded detection.

1992 ◽  
Vol 49 (10) ◽  
pp. 2196-2218 ◽  
Author(s):  
Kirk O. Winemiller ◽  
Kenneth A. Rose

Interspecific patterns of fish life histories were evaluated in relation to several theoretical models of life-history evolution. Data were gathered for 216 North American fish species (57 families) to explore relationships among variables and to ordinate species. Multivariate tests, performed on freshwater, marine, and combined data matrices, repeatedly identified a gradient associating later-maturing fishes with higher fecundity, small eggs, and few bouts of reproduction during a short spawning season and the opposite suite of traits with small fishes. A second strong gradient indicated positive associations between parental care, egg size, and extended breeding seasons. Phylogeny affected each variable, and some higher taxonomic groupings were associated with particular life-history strategies. High-fecundity characteristics tended to be associated with large species ranges in the marine environment. Age at maturation, adult growth rate, life span, and egg size positively correlated with anadromy. Parental care was inversely correlated with median latitude. A trilateral continuum based on essential trade-offs among three demographic variables predicts many of the correlations among life-history traits. This framework has implications for predicting population responses to diverse natural and anthropogenic disturbances and provides a basis for comparing responses of different species to the same disturbance.


2009 ◽  
Vol 364 (1523) ◽  
pp. 1499-1509 ◽  
Author(s):  
Shripad Tuljapurkar ◽  
Jean-Michel Gaillard ◽  
Tim Coulson

Environmental stochasticity is known to play an important role in life-history evolution, but most general theory assumes a constant environment. In this paper, we examine life-history evolution in a variable environment, by decomposing average individual fitness (measured by the long-run stochastic growth rate) into contributions from average vital rates and their temporal variation. We examine how generation time, demographic dispersion (measured by the dispersion of reproductive events across the lifespan), demographic resilience (measured by damping time), within-year variances in vital rates, within-year correlations between vital rates and between-year correlations in vital rates combine to determine average individual fitness of stylized life histories. In a fluctuating environment, we show that there is often a range of cohort generation times at which the fitness is at a maximum. Thus, we expect ‘optimal’ phenotypes in fluctuating environments to differ from optimal phenotypes in constant environments. We show that stochastic growth rates are strongly affected by demographic dispersion, even when deterministic growth rates are not, and that demographic dispersion also determines the response of life-history-specific average fitness to within- and between-year correlations. Serial correlations can have a strong effect on fitness, and, depending on the structure of the life history, may act to increase or decrease fitness. The approach we outline takes a useful first step in developing general life-history theory for non-constant environments.


2020 ◽  
Vol 375 (1803) ◽  
pp. 20190492 ◽  
Author(s):  
Dominik Deffner ◽  
Richard McElreath

Social learning and life history interact in human adaptation, but nearly all models of the evolution of social learning omit age structure and population regulation. Further progress is hindered by a poor appreciation of how life history affects selection on learning. We discuss why life history and age structure are important for social learning and present an exemplary model of the evolution of social learning in which demographic properties of the population arise endogenously from assumptions about per capita vital rates and different forms of population regulation. We find that, counterintuitively, a stronger reliance on social learning is favoured in organisms characterized by ‘fast’ life histories with high mortality and fertility rates compared to ‘slower’ life histories typical of primates. Long lifespans make early investment in learning more profitable and increase the probability that the environment switches within generations. Both effects favour more individual learning. Additionally, under fertility regulation (as opposed to mortality regulation), more juveniles are born shortly after switches in the environment when many adults are not adapted, creating selection for more individual learning. To explain the empirical association between social learning and long life spans and to appreciate the implications for human evolution, we need further modelling frameworks allowing strategic learning and cumulative culture. This article is part of the theme issue ‘Life history and learning: how childhood, caregiving and old age shape cognition and culture in humans and other animals’.


2005 ◽  
Vol 62 (4) ◽  
pp. 872-885 ◽  
Author(s):  
Kirk O Winemiller

Life history theories attempt to explain the evolution of organism traits as adaptations to environmental variation. A model involving three primary life history strategies (endpoints on a triangular surface) describes general patterns of variation more comprehensively than schemes that examine single traits or merely contrast fast versus slow life histories. It provides a general means to predict a priori the types of populations with high or low demographic resilience, production potential, and conformity to density-dependent regulation. Periodic (long-lived, high fecundity, high recruitment variation) and opportunistic (small, short-lived, high reproductive effort, high demographic resilience) strategies should conform poorly to models that assume density-dependent recruitment. Periodic-type species reveal greatest recruitment variation and compensatory reserve, but with poor conformity to stock–recruitment models. Equilibrium-type populations (low fecundity, large egg size, parental care) should conform better to assumptions of density-dependent recruitment, but have lower demographic resilience. The model's predictions are explored relative to sustainable harvest, endangered species conservation, supplemental stocking, and transferability of ecological indices. When detailed information is lacking, species ordination according to the triangular model provides qualitative guidance for management and development of more detailed predictive models.


2007 ◽  
Vol 55 (3) ◽  
pp. 261 ◽  
Author(s):  
Eric S. Menges

In this work, I have used life-history and demographic data to define fire return intervals for several types of Florida scrub, a xeric shrubland where fire is the dominant ecological disturbance but where fire suppression is a major issue. The datasets combine chronosequence and longitudinal approaches at community and population levels. Resprouting shrubs, which dominate most types of Florida scrub, recover rapidly after fires (although their limits under frequent fires are not well known) and also increasingly dominate long-unburned areas. These dominant shrubs can prosper over a range of fire return intervals. Obligate-seeding scrub plants, which often have persistent seed banks, can be eliminated by frequent fire but often decline with infrequent fire. Population viability analyses of habitat specialists offer more precision in suggesting ranges of appropriate fire return intervals. For two types of Florida scrub (rosemary scrub and oak–hickory scrub), plant-population viability analyses narrow the interval and suggest more frequent fires than do previous recommendations, at intervals of 15–30 and 5–12 years, respectively. Variation in fire regimes in time and space (pyrodiversity) is recommended as a bet-hedging fire-management strategy and to allow co-existence of species with disparate life histories.


2006 ◽  
Vol 273 (1605) ◽  
pp. 3065-3073 ◽  
Author(s):  
Thomas F Turner ◽  
Megan J Osborne ◽  
Gregory R Moyer ◽  
Melissa A Benavides ◽  
Dominique Alò

Successful recovery and sustainability of threatened and exploited species depends in part on retention and maintenance of genetic diversity. Theory indicates that genetic diversity is lost at a rate inversely proportional to the genetically effective population size ( N e ), which is roughly equal to one-half the adult census size ( N ) in many organisms. However, N e has been reported to be up to five orders of magnitude lower than N in species with life histories that result in type III survivorship (high fecundity, but heavy mortality in early life stages, e.g. bony fishes), prompting speculation that low values of N e may be a general feature of such organisms despite sometimes vast abundances. Here, we compared N e and the ratio N e / N across three ecologically similar fish species from the arid southwestern United States, all with type III life histories but with differing expectations of egg and larval survivorship that correlate with the degree of human-imposed habitat fragmentation. Our study indicates that type III life history may be necessary, but this alone is insufficient to account for extraordinarily low values of N e / N . Rather, life history interacts with environmentally imposed mortality to determine the rate and magnitude of change in genetic diversity in these desert fish species.


2015 ◽  
Author(s):  
Ryan Baldini

A common belief among human life history researchers is that "harsher" environments - i.e., those with higher mortality rates and resource stress - select for "fast" life histories, i.e. earlier reproduction and faster senescence. I show that these "harsh environments, fast life histories" - or HEFLH - hypotheses are poorly supported by evolutionary theory. First, I use a simple model to show that effects of environmental harshness on life history evolution are incredibly diverse. In particular, small changes in basic but poorly understood variables - e.g., whether and how population density affects vital rates - can cause selection to favor very different life histories. Furthermore, I show that almost all life history theory used to justify HEFLH hypotheses is misapplied in the first place. The reason is that HEFLH hypotheses usually treat plastic responses to heterogeneous environmental conditions within a population, whereas the theory used to justify such hypotheses treat genetic responses to environmental changes across an entire population. Counter-intuitively, the predictions of the former do not generally apply to the latter: the optimal response to a harsh environment within a large heterogeneous environment is not necessarily the optimal strategy of a population uniformly inhabiting the same harsh environment. I discuss these theoretical results in light of the current state of empirical research.


2021 ◽  
Author(s):  
Christie Le Coeur ◽  
Nigel Gilles Yoccoz ◽  
Roberto Salguero-Gomez ◽  
Yngvild Vindenes

Demographic buffering and lability have both been identified as important adaptive strategies to optimise long-term fitness in variable environments. These strategies are not mutually exclusive, however we lack efficient methods to measure their relative importance. Here, we define a new index to measure the total lability for a given life history, and use stochastic simulations to disentangle relative fitness effects of buffering and lability. The simulations use 81 animal matrix population models, and different scenarios to explore how the strategies vary across life histories. The highest potential for adaptive demographic lability was found for short- to intermediately long-lived species, while demographic buffering was the main response in slow-living species. This study suggests that faster-living species are more responsive to environmental variability, both for positive or negative effects. Our methods and results provide a more comprehensive view of adaptations to variability, of high relevance to predict species responses to climate change.


Author(s):  
Maren N. Vitousek ◽  
Laura A. Schoenle

Hormones mediate the expression of life history traits—phenotypic traits that contribute to lifetime fitness (i.e., reproductive timing, growth rate, number and size of offspring). The endocrine system shapes phenotype by organizing tissues during developmental periods and by activating changes in behavior, physiology, and morphology in response to varying physical and social environments. Because hormones can simultaneously regulate many traits (hormonal pleiotropy), they are important mediators of life history trade-offs among growth, reproduction, and survival. This chapter reviews the role of hormones in shaping life histories with an emphasis on developmental plasticity and reversible flexibility in endocrine and life history traits. It also discusses the advantages of studying hormone–behavior interactions from an evolutionary perspective. Recent research in evolutionary endocrinology has provided insight into the heritability of endocrine traits, how selection on hormone systems may influence the evolution of life histories, and the role of hormonal pleiotropy in driving or constraining evolution.


2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Silu Lin ◽  
Jana Werle ◽  
Judith Korb

AbstractOrganisms are typically characterized by a trade-off between fecundity and longevity. Notable exceptions are social insects. In insect colonies, the reproducing caste (queens) outlive their non-reproducing nestmate workers by orders of magnitude and realize fecundities and lifespans unparalleled among insects. How this is achieved is not understood. Here, we identified a single module of co-expressed genes that characterized queens in the termite species Cryptotermes secundus. It encompassed genes from all essential pathways known to be involved in life-history regulation in solitary model organisms. By manipulating its endocrine component, we tested the recent hypothesis that re-wiring along the nutrient-sensing/endocrine/fecundity axis can account for the reversal of the fecundity/longevity trade-off in social insect queens. Our data from termites do not support this hypothesis. However, they revealed striking links to social communication that offer new avenues to understand the re-modelling of the fecundity/longevity trade-off in social insects.


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