Dimensionless numbers and the assembly rules for life histories

1991 ◽  
Vol 332 (1262) ◽  
pp. 41-48 ◽  
Keyword(s):  
Life History ◽  
Life Histories ◽  
Life History Theory ◽  
Assembly Rules ◽  
Dimensionless Numbers ◽  
Age Of Maturity

This paper reviews recent efforts to use certain dimensionless numbers (DLNs) to classify life histories in plants and animals. These DLNs summarize the relation between growth, mortality and maturation, and several groups of animals show interesting patterns with respect to their numeric values. Finally we focus on one DLN, the product of the age of maturity and the adult instantaneous mortality, to show how evolutionary life history theory may be used to predict the value of the DLN, which differs greatly between major groups of animals.

A Primer of Life Histories

2021 ◽  
Author(s):  
Jeffrey A. Hutchings
Keyword(s):  
Life History ◽  
Life Histories ◽  
Life History Theory ◽  
Life History Traits ◽  
Reproductive Effort ◽  
Effective Means ◽  
Academic Experience ◽  
Sustainable Exploitation ◽  
Evolution Of Life ◽  
Opportune Time

Life histories describe how genotypes schedule their reproductive effort throughout life in response to factors that affect their survival and fecundity. Life histories are solutions that selection has produced to solve the problem of how to persist in a given environment. These solutions differ tremendously within and among species. Some organisms mature within months of attaining life, others within decades; some produce few, large offspring as opposed to numerous, small offspring; some reproduce many times throughout their lives while others die after reproducing just once. The exponential pace of life-history research provides an opportune time to engage and re-engage new generations of students and researchers on the fundamentals and applications of life-history theory. Chapters 1 through 4 describe the fundamentals of life-history theory. Chapters 5 through 8 focus on the evolution of life-history traits. Chapters 9 and 10 summarize how life-history theory and prediction has been applied within the contexts of conservation and sustainable exploitation. This primer offers an effective means of rendering the topic accessible to readers from a broad range of academic experience and research expertise.

scholarly journals Towards cancer-aware life-history modelling

2015 ◽  
Vol 370 (1673) ◽  
pp. 20140234 ◽  
Author(s):  
Hanna Kokko ◽  
Michael E. Hochberg
Keyword(s):  
Life History ◽  
Life Histories ◽  
Life History Theory ◽  
Cancer Susceptibility ◽  
Natural Populations ◽  
Sexually Dimorphic ◽  
Adaptive Responses ◽  
Extrinsic Mortality ◽  
Size Evolution ◽  
In The Wild

Studies of body size evolution, and life-history theory in general, are conducted without taking into account cancer as a factor that can end an organism's reproductive lifespan. This reflects a tacit assumption that predation, parasitism and starvation are of overriding importance in the wild. We argue here that even if deaths directly attributable to cancer are a rarity in studies of natural populations, it remains incorrect to infer that cancer has not been of importance in shaping observed life histories. We present first steps towards a cancer-aware life-history theory, by quantifying the decrease in the length of the expected reproductively active lifespan that follows from an attempt to grow larger than conspecific competitors. If all else is equal, a larger organism is more likely to develop cancer, but, importantly, many factors are unlikely to be equal. Variations in extrinsic mortality as well as in the pace of life—larger organisms are often near the slow end of the fast–slow life-history continuum—can make realized cancer incidences more equal across species than what would be observed in the absence of adaptive responses to cancer risk (alleviating the so-called Peto's paradox). We also discuss reasons why patterns across species can differ from within-species predictions. Even if natural selection diminishes cancer susceptibility differences between species, within-species differences can remain. In many sexually dimorphic cases, we predict males to be more cancer-prone than females, forming an understudied component of sexual conflict.

scholarly journals Between semelparity and iteroparity: empirical evidence for a continuum of modes of parity

2017 ◽  
Author(s):  
P. William Hughes
Keyword(s):  
Life History ◽  
Mathematical Models ◽  
Molecular Basis ◽  
Life Histories ◽  
Life History Theory ◽  
Reproductive Effort ◽  
Theoretical Biology ◽  
Relative Fitness ◽  
Life History Strategies ◽  
Molecular Evidence

ABSTRACTThe number of times an organism reproduces (i.e. its mode of parity) is a fundamental life-history character, and evolutionary and ecological models that compare the relative fitness of strategies are common in life history theory and theoretical biology. Despite the success of mathematical models designed to compare intrinsic rates of increase between annual-semelparous and perennial-iteroparous reproductive schedules, there is widespread evidence that variation in reproductive allocation among semelparous and iteroparous organisms alike is continuous. This paper reviews the ecological and molecular evidence for the continuity and plasticity of modes of parity––that is, the idea that annual-semelparous and perennial-iteroparous life histories are better understood as endpoints along a continuum of possible strategies. I conclude that parity should be understood as a continuum of different modes of parity, which differ by the degree to which they disperse or concentrate reproductive effort in time. I further argue that there are three main implications of this conclusion: (1) That seasonality should not be conflated with parity; (2) that mathematical models purporting to explain the evolution of semelparous life histories from iteroparous ones (or vice versa) should not assume that organisms can only display either an annual-semelparous life history or a perennial-iteroparous one; and (3) that evolutionary ecologists should examine the physiological or molecular basis of traits underlying different modes of parity, in order to obtain a general understanding of how different life history strategies can evolve from one another.

Can commercial fishing cause evolution? Answers from guppies (Poecilia reticulata)

2005 ◽  
Vol 62 (4) ◽  
pp. 791-801 ◽  
Author(s):  
David N Reznick ◽  
Cameron K Ghalambor
Keyword(s):  
Life History ◽  
Body Size ◽  
Life Histories ◽  
Life History Theory ◽  
Poecilia Reticulata ◽  
Mortality Rates ◽  
Adult Mortality ◽  
Commercial Fisheries ◽  
Commercial Fishing ◽  
Rate Of Evolution

Life history theory predicts that high adult mortality rates select for earlier maturity and increased reproduction. If such evolution occurs in response to the commercial exploitation of natural fish populations, then the correlated reduction in body size would reduce the yield of the fishery. Earlier maturity and reduced body size are seen in commercially exploited populations. Here, we compare the life histories of natural populations of guppies (Poecilia reticulata) from Trinidad that live in either high- or low-predation environments, which serve as surrogates for the presence or absence of commercial fishing. We can quantify mortality rate and life history variables, including age and size at maturity, in the laboratory and in nature. We have manipulated mortality rates in nature and measured the rate of evolution. High mortality selects for earlier maturity at a smaller size, as observed in commercial fisheries and as predicted by theory. Furthermore, the nature and magnitude of predator-induced mortality are comparable to those caused by commercial fishing. The rate of evolution in guppies predicts similar evolution in commercial fisheries on a time scale of decades. These attributes support arguments that humans, like predators, have acted as an agent of selection when exploiting populations of fish.

scholarly journals Lack, Skutch, and Moreau: The Early Development of Life-History Thinking

The Condor ◽  
2000 ◽  
Vol 102 (1) ◽  
pp. 3-8 ◽  
Author(s):  
Robert E. Ricklefs
Keyword(s):  
Life History ◽  
Life Histories ◽  
Life History Theory ◽  
Life History Evolution ◽  
Early Life History ◽  
Nesting Success ◽  
Evolutionary Forces ◽  
Full Development ◽  
The Rich ◽  
David Lack

Abstract Papers by Reginald Moreau, David Lack, and Alexander Skutch published during the 1940s set the stage for the development of thinking about life histories over the following decades. Lack was concerned about the fundamental issue of individual vs. group selection and turned life-history evolution into a battleground for this debate. His monolithic focus on nesting success as a measure of fitness and on food availability as the principal determinant of nesting success obscured the rich empirical background brought to the debate by Skutch and the diverse evolutionary forces envisioned by Moreau. Lack's strong convictions, single-mindedness, and eloquence forced biologists to confront several important problems but also held back the full development of life-history theory until the mid-1960s. Retrospective consideration of these early life-history studies shows how science can progress through a balance of conviction and reflection.

Divergent life histories and other ecological adaptations: Examples of social-class differences in attention, cognition, and attunement to others

2017 ◽  
Vol 40 ◽  
Author(s):  
Igor Grossmann ◽  
Michael E. W. Varnum
Keyword(s):  
Socioeconomic Status ◽  
Life History ◽  
Social Class ◽  
Life Histories ◽  
Life History Theory ◽  
Psychological Effects ◽  
Life History Strategies ◽  
Class Differences ◽  
Ecological Adaptations

AbstractMany behavioral and psychological effects of socioeconomic status (SES), beyond those presented by Pepper & Nettle cannot be adequately explained by life-history theory. We review such effects and reflect on the corresponding ecological affordances and constraints of low- versus high-SES environments, suggesting that several ecology-specific adaptations, apart from life-history strategies, are responsible for the behavioral and psychological effects of SES.

scholarly journals Drought frequency predicts life history strategies in Heliophila

2018 ◽  
Author(s):  
J. Grey Monroe ◽  
Brian Gill ◽  
Kathryn Turner ◽  
John K McKay
Keyword(s):  
Life History ◽  
Life Histories ◽  
Evolutionary Biology ◽  
Life History Theory ◽  
Life History Strategy ◽  
Empirical Support ◽  
Life History Strategies ◽  
Perennial Species ◽  
Drought Frequency ◽  
Occurrence Records

Explaining variation in life history strategies is a long-standing goal of evolutionary biology. For plants, annual and perennial life histories are thought to reflect adaptation to environments that differ in the frequency of stress events such as drought. Here we test this hypothesis in Heliophila (Brassicaceae), a diverse genus of flowering plants native to Africa, by integrating 34 years of satellite-based drought measurements with 2192 herbaria occurrence records. Consistent with predictions from classic life history theory, we find that perennial Heliophila species occur in environments where droughts are significantly less frequent compared to annuals. These associations are predictive while controlling for phylogeny, lending support to the hypothesis that drought related natural selection has influenced the distributions of these strategies. Additionally, the collection dates of annual and perennial species indicate that annuals escape drought prone seasons during the seed phase of their life cycle. Together, these findings provide empirical support for classic hypotheses about the drivers of life history strategy in plants - that perennials out compete annuals in environments with less frequent drought and that annuals are adapted to environments with more frequent drought by escaping drought prone seasons as seeds.

Variation in the reproductive rate of bats

2004 ◽  
Vol 82 (5) ◽  
pp. 688-693 ◽  
Author(s):  
Robert M.R Barclay ◽  
Joel Ulmer ◽  
Cameron J.A MacKenzie ◽  
Megan S Thompson ◽  
Leif Olson ◽  
...  
Keyword(s):  
Life History ◽  
Life Histories ◽  
Life History Theory ◽  
Life History Traits ◽  
Prey Availability ◽  
Weather Conditions ◽  
Reproductive Rate ◽  
Tropical Species ◽  
Allocation Of Resources ◽  
Reproductive Rates

In many respects, bats have relatively slow life histories. However, the reproductive rate of bats (i.e., the proportion of females that reproduce in any breeding season) has not been critically examined. We compiled data on the reproductive rates of bats to test predictions based on life-history theory. Among 257 samples from 103 species, reproductive rate varied considerably and was typically under 100%. Temperate-zone species had significantly lower and more variable reproductive rates than did tropical species. Reproductive rate also varied among families, with species in the Vespertilionidae having particularly high rates. As predicted based on life-history theory, reproductive rate was negatively correlated with longevity, and among vespertilionids, species with larger litters had higher reproductive rates. Thus, the data suggest that bats have relatively slow reproductive rates and, as in other life-history traits, fall at the "slow" end of the fast–slow life-history continuum found among mammals. Female bats, especially those in temperate regions, appear to adjust their allocation of resources to reproduction, and at times forego reproduction, perhaps in relation to their body condition, prey availability, and weather conditions.

scholarly journals Nutrition shapes life-history evolution across species

2016 ◽  
Vol 283 (1834) ◽  
pp. 20152764 ◽  
Author(s):  
Eli M. Swanson ◽  
Anne Espeset ◽  
Ihab Mikati ◽  
Isaac Bolduc ◽  
Robert Kulhanek ◽  
...  
Keyword(s):  
Life History ◽  
Life Histories ◽  
Host Plants ◽  
Life History Theory ◽  
Life History Evolution ◽  
Sodium Content ◽  
Testis Size ◽  
Eye Size ◽  
History Evolution ◽  
Diet Shifts

Nutrition is a key component of life-history theory, yet we know little about how diet quality shapes life-history evolution across species. Here, we test whether quantitative measures of nutrition are linked to life-history evolution across 96 species of butterflies representing over 50 independent diet shifts. We find that butterflies feeding on high nitrogen host plants as larvae are more fecund, but their eggs are smaller relative to their body size. Nitrogen and sodium content of host plants are also both positively related to eye size. Some of these relationships show pronounced lineage-specific effects. Testis size is not related to nutrition. Additionally, the evolutionary timing of diet shifts is not important, suggesting that nutrition affects life histories regardless of the length of time a species has been adapting to its diet. Our results suggest that, at least for some lineages, species with higher nutrient diets can invest in a range of fitness-related traits like fecundity and eye size while allocating less to each egg as offspring have access to a richer diet. These results have important implications for the evolution of life histories in the face of anthropogenic changes in nutrient availability.

The Evolution of Annual and Perennial Plant Life Histories: Ecological Correlates and Genetic Mechanisms

2020 ◽  
Vol 51 (1) ◽  
pp. 461-481 ◽  
Author(s):  
Jannice Friedman
Keyword(s):  
Life History ◽  
Life Histories ◽  
Life History Theory ◽  
Life History Strategies ◽  
Developmental Genetics ◽  
Evolutionary Transitions ◽  
Perennial Plant ◽  
Genetic Mechanisms ◽  
Future Reproduction ◽  
One Year

Flowering plants exhibit two principal life-history strategies: annuality (living and reproducing in one year) and perenniality (living more than one year). The advantages of either strategy depend on the relative benefits of immediate reproduction balanced against survivorship and future reproduction. This trade-off means that life-history strategies are associated with particular environments, with annuals being found more often in unpredictable habitats. Annuality and perenniality are the outcome of developmental genetic programs responding to their environment, with perennials being distinguished by their delayed competence to flower and reversion to growth after flowering. Evolutionary transitions between these strategies are frequent and have consequences for mating systems and genome evolution, with perennials being more likely to outcross with higher inbreeding depression and lower rates of molecular evolution. Integrating expectations from life-history theory with knowledge of the developmental genetics of flowering and seasonality is required to understand the mechanisms involved in the evolution of annual and perennial life histories.

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