Adaptive, genetically based differences in life history between estuary and freshwater threespine sticklebacks (Gasterosteus aculeatus L.)

1989 ◽  
Vol 67 (10) ◽  
pp. 2448-2454 ◽  
Author(s):  
Randal J. Snyder ◽  
Hugh Dingle
Keyword(s):  
Life History ◽  
Life Histories ◽  
Life History Theory ◽  
Gasterosteus Aculeatus ◽  
Genetic Variance ◽  
The Body ◽  
Life Styles ◽  
First Reproduction ◽  
Freshwater Population ◽  
Threespine Sticklebacks

Life history theory predicts that migratory fishes should delay reproduction, be larger at maturity, and have higher fecundities than nonmigrants. We tested this hypothesis by comparing life histories of laboratory-reared estuary and freshwater threespine sticklebacks (Gasterosteus aculeatus L.) from the Navarro River, California. We also estimated phenotypic correlations and genetic variance (broad-sense heritabilities) for reproductive characteristics of these fish. The more migratory estuary sticklebacks delayed reproduction, were larger at first reproduction, and had higher fecundities than the freshwater fish. We found no significant differences in interclutch interval or average size of eggs. The body size – fecundity relationship did not differ among these populations, unlike the findings in previous reports comparing anadromous and freshwater threespine sticklebacks. We found significant levels of genetic variance for age and size at first reproduction in both populations, and for fecundity in the freshwater population. The estuary and freshwater sticklebacks did not differ in average number of fin rays, gill rakers, or lateral plates, indicating that differentiation in life history has not been accompanied by significant changes in these characteristics. These results provide evidence of genetic divergence between these populations with respect to life histories, and the nature of these differences suggests that adaptation to different migratory life-styles has occurred.

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.

Reproductive-timing-dependent alternation of offspring life histories in female threespine sticklebacks

1999 ◽  
Vol 77 (8) ◽  
pp. 1314-1321 ◽  
Author(s):  
Toshihiko Saito ◽  
Shigeru Nakano
Keyword(s):  
Life Histories ◽  
Gasterosteus Aculeatus ◽  
Reproductive Timing ◽  
Equivalent Age ◽  
Structured Population ◽  
Otolith Increments ◽  
Threespine Sticklebacks ◽  
Young Of The Year ◽  
Age Structured ◽  
Breeding Seasons

Relationships between reproductive timing of spawners and timing of hatch and age at maturity of their offspring were examined in fluvial threespine sticklebacks, Gasterosteus aculeatus. Some age 2 and all age 3 females matured in this age-structured population, with only a few females reproducing over two successive breeding seasons. Age 2 females spawned over the relatively long breeding season (March-August), whereas age 3 females spawned mainly early in the season (March-June). Although the standard length of mature age 3 females was greater than that of age 2 females, the back-calculated standard lengths of the former were always shorter than those of the latter at an equivalent age, the most distinct differences being apparent in young of the year. Analysis of daily otolith increments showed that the earlier the young of the year were born, the larger they were at the end of the growing season. As a result of these findings, age 3 females can be expected to produce offspring that will mature at age 2, whereas the offspring of late-spawning age 2 females are more likely to mature at age 3. Therefore, a partial alternation of life histories between generations is thought to occur.

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.

The Evolution of Life History Parameters in Teleosts

1984 ◽  
Vol 41 (6) ◽  
pp. 989-1000 ◽  
Author(s):  
Derek A. Roff
Keyword(s):  
Growth Rate ◽  
Life History ◽  
Life History Theory ◽  
Larval Survival ◽  
Reasonable Assumption ◽  
Natural Mortality ◽  
Age At First Reproduction ◽  
Life History Parameters ◽  
First Case ◽  
First Reproduction

Empirical studies have shown that in teleosts there is a significant correlation between the life history parameters, age at first reproduction, natural mortality, and growth rate. In this paper 1 hypothesize that these correlations are the result of evolutionary adjustments due to the trade-off between reproduction, growth, and survival. A simple and reasonable assumption is that the costs of reproduction are sufficient to cause the ltmt function to decrease. A simple expression relating the age at first reproduction is derived from this assumption. This formula accounts for a statistically significant portion (60.6%) of the variation in age at first reproduction in 30 stocks of fish. To extend the model to predict the distribution of life history parameters across all teleosts, an explicit cost function is incorporated. The model is analyzed with respect to two fitness measures, the expected lifetime fecundity and malthusian parameter, r. In the first case it is shown that the optimal age at maturity, T, depends only on the natural mortality rate (M) and the growth rate (k). In the second case, T is a function of k and the logarithm of a parameter, In C; the latter is a product of egg and larval survival, maximum body length (Lx), and the proportionality coefficient of the fecundity/length function. Difficulties of measuring egg and larval survival make the testing of the latter case difficult for particular species. However, this method provides a simple formula for the computation of r; this is shown generally to be approximately zero, thereby adding strength to the assumptions of the first analysis. The distribution patterns of T on k and M on k are predicted and compared with the observed pattern. In general, the predictions are validated: however, certain combinations of k and ln C are shown to occur very infrequently. The prediction of such "empty" regions of the parameter space remains a challenge for future development of life history theory.

Evolutionary history of threespine sticklebacks (Gasterosteus spp.) in British Columbia: insights from a physiological clock

1995 ◽  
Vol 73 (11) ◽  
pp. 2154-2158 ◽  
Author(s):  
Rees Kassen ◽  
Dolph Schluter ◽  
John Donald McPhail
Keyword(s):  
British Columbia ◽  
Fresh Water ◽  
Evolutionary History ◽  
Egg Size ◽  
Gasterosteus Aculeatus ◽  
Salt Water ◽  
Freshwater Invasion ◽  
Freshwater Population ◽  
Threespine Sticklebacks ◽  
History Of

Geologic and allozyme evidence suggests that threespine sticklebacks (Gasterosteus aculeatus complex) in low-lying southwestern British Columbia lakes were founded during two incursions of marine sticklebacks after the retreat of the Pleistocene glaciers (the double-invasion hypothesis). We used the salinity tolerance of embryos, measured as hatchability in salt water, to establish the relative order of freshwater invasion by marine sticklebacks and to test the double-invasion hypothesis. Limnetics and an anadromous population hatched nearly equivalent numbers of young in salt water as in fresh water, whereas benthics and one solitary freshwater population had low hatchability in salt water. We also found that eggs from freshwater populations were larger than those from marine populations and limnetics had smaller eggs than benthics and the solitary population. These results support the double-invasion hypothesis and suggest a trend of increasing egg size with increasing time spent in fresh water.

scholarly journals Trade-off between age of first reproduction and survival in a female primate

2009 ◽  
Vol 5 (3) ◽  
pp. 339-342 ◽  
Author(s):  
Gregory E. Blomquist
Keyword(s):  
Life History ◽  
Life History Theory ◽  
Rhesus Macaques ◽  
Human Study ◽  
Genetic Correlations ◽  
Adult Survival ◽  
Trade Off ◽  
Trade Offs ◽  
Female Life History ◽  
First Reproduction

Trade-offs are central to life-history theory but difficult to document. Patterns of phenotypic and genetic correlations in rhesus macaques, Macaca mulatta —a long-lived, slow-reproducing primate—are used to test for a trade-off between female age of first reproduction and adult survival. A strong positive genetic correlation indicates that female macaques suffer reduced adult survival when they mature relatively early and implies primate senescence can be explained, in part, by antagonistic pleiotropy. Contrasts with a similar human study implicate the extension of parental effects to later ages as a potential mechanism for circumventing female life-history trade-offs in human evolution.

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.

Spatial variation of morphology in a freshwater population of the threespine stickleback, Gasterosteus aculeatus

1992 ◽  
Vol 70 (6) ◽  
pp. 1140-1148 ◽  
Author(s):  
Jeffrey V. Baumgartner
Keyword(s):  
Gasterosteus Aculeatus ◽  
Lateral Plate ◽  
Coastal System ◽  
Body Form ◽  
Evolutionary Forces ◽  
Freshwater Population ◽  
Threespine Sticklebacks ◽  
Functional Components ◽  
Significant Size ◽  
Lateral Plates

Differentiation with respect to two functional components of morphology, the defensive complex and overall body form, was studied in a population of threespine sticklebacks (Gasterosteus aculeatus) from the Brush Creek drainage, a small coastal system in northern California with high- and low-gradient habitats. The vast majority of body-shape differences among localities was accounted for by size-related allometric variation, the differences being closely related to overall growth trends. Relative to general body size, small individuals had long spines and fins whereas larger individuals tended to be deep bodied and have shorter fins and shorter spines. Significant size-independent differentiation with respect to the defensive complex and overall body form was also observed. The spatial pattern of differentiation in the components of the defensive complex changed dramatically over the period of study, possibly in response to natural selection. Stable stepped clines for overall body form and lateral-plate morph ratio were observed. Both clines were centered on the ecotone between high- and low-gradient habitats, and were apparently maintained by differential selection in alternative stream-gradient habitats despite gene flow across the ecotone. Sticklebacks from the high-gradient habitat had a continuous row of lateral plates, were elongate, and had long fins, whereas those from the low-gradient or standing-water habitat tended to have only abdominal plates, were more robust through the midbody, and had shorter fins. The results of this study and previous work suggest that various aspects of stickleback morphology may respond independently and rapidly to different evolutionary forces and be functionally related to hydrodynamics.

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.

scholarly journals Life-history theory, chronic childhood illness and the timing of first reproduction in a British birth cohort

2012 ◽  
Vol 279 (1740) ◽  
pp. 2998-3002 ◽  
Author(s):  
David Waynforth
Keyword(s):  
Life History ◽  
Chronic Disease ◽  
Life Expectancy ◽  
Life History Theory ◽  
Pubertal Development ◽  
Experimental Studies ◽  
Past Research ◽  
Theoretical Models ◽  
Age At First Reproduction ◽  
First Reproduction

Life-history theoretical models show that a typical evolutionarily optimal response of a juvenile organism to high mortality risk is to reach reproductive maturity earlier. Experimental studies in a range of species suggest the existence of adaptive flexibility in reproductive scheduling to maximize fitness just as life-history theory predicts. In humans, supportive evidence has come from studies comparing neighbourhoods with different mortality rates, historical and cross-cultural data. Here, the prediction is tested in a novel way in a large ( n = 9099), longitudinal sample using data comparing age at first reproduction in individuals with and without life-expectancy-reducing chronic disease diagnosed during childhood. Diseases selected for inclusion as chronic illnesses were those unlikely to be significantly affected by shifting allocation of effort away from reproduction towards survival; those which have comparatively large effects on mortality and life expectancy; and those which are not profoundly disabling. The results confirmed the prediction that chronic disease would associate with early age at first reproduction: individuals growing up with a serious chronic disease were 1.6 times more likely to have had a first child by age 30. Analysis of control variables also confirmed past research findings on links between being raised father-absent and early pubertal development and reproduction.

Sign in / Sign up

Export Citation Format

Share Document