Predicting Natural Mortality Rates and Reproduction–Mortality Trade-offs from Fish Life History Data

1983 ◽  
Vol 40 (5) ◽  
pp. 612-620 ◽  
Author(s):  
R. A. Myers ◽  
R. W. Doyle
Keyword(s):  
Life History ◽  
Life Histories ◽  
Optimization Techniques ◽  
Evolutionary Constraint ◽  
Natural Mortality ◽  
Life History Data ◽  
Trade Offs ◽  
Conversion Efficiencies ◽  
Evolutionarily Stable ◽  
Mortality Estimates

A method for estimating natural mortality and evolutionary constraint on fish life histories is presented based on the assumption that observed life histories are evolutionarily stable. Inverse optimization techniques are used to determine the values of natural mortality, reproduction–mortality trade-offs, and energy conversion efficiencies that would make observed life histories evolutionarily stable. The life history method yields natural mortality estimates comparable with those based on population age–frequency data. Sensitivity analysis is used to determine the robustness of the predictions to errors in parameter estimation and density-dependent factors.

Modelling fishing-induced adaptations and consequences for natural mortality

2010 ◽  
Vol 67 (7) ◽  
pp. 1086-1097 ◽  
Author(s):  
Christian Jørgensen ◽  
Øyvind Fiksen
Keyword(s):  
Life History ◽  
Body Size ◽  
Life Histories ◽  
Life History Traits ◽  
Reproductive Behaviour ◽  
Natural Mortality ◽  
Fishing Mortality ◽  
Trade Offs ◽  
Wide Range ◽  
Investment In Reproduction

When trade-offs involving predation and mortality are perturbed by human activities, behaviour and life histories are expected to change, with consequences for natural mortality rates. We present a general life history model for fish in which three common relationships link natural mortality to life history traits and behaviour. First, survival increases with body size. Second, survival declines with growth rate due to risks involved with resource acquisition and allocation. Third, fish that invest heavily in reproduction suffer from decreased survival due to costly reproductive behaviour or morphology that makes escapes from predators less successful. The model predicts increased natural mortality rate as an adaptive response to harvesting. This extends previous models that have shown that harvesting may cause smaller body size, higher growth rates, and higher investment in reproduction. The predicted increase in natural mortality is roughly half the fishing mortality over a wide range of harvest levels and parameter combinations such that fishing two fish kills three after evolutionary adaptations have taken place.

Hormones and Behavior

2019 ◽  
pp. 11-26
Author(s):  
Maren N. Vitousek ◽  
Laura A. Schoenle
Keyword(s):  
Life History ◽  
Life Histories ◽  
Life History Traits ◽  
Developmental Plasticity ◽  
Endocrine System ◽  
Phenotypic Traits ◽  
Social Environments ◽  
Trade Offs ◽  
And Behavior

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.

Life histories of North American game birds: a reanalysis

1988 ◽  
Vol 66 (8) ◽  
pp. 1906-1912 ◽  
Author(s):  
Todd W. Arnold
Keyword(s):  
Life History ◽  
North American ◽  
Life Histories ◽  
Life History Traits ◽  
Reproductive Effort ◽  
Cost Of Reproduction ◽  
Reproductive Value ◽  
Trade Offs ◽  
Game Birds ◽  
The Cost

Recently, Zammuto (R. M. Zammuto. 1986. Can. J. Zool. 64: 2739–2749) suggested that North American game birds exhibited survival–fecundity trade-offs consistent with the "cost of reproduction" hypothesis. However, there were four serious problems with the data and the analyses that Zammuto used: (i) the species chosen for analysis ("game birds") showed little taxonomic or ecological uniformity, (ii) the measures of future reproductive value (maximum longevity) were severely biased by unequal sample sizes of band recoveries, (iii) the measures of current reproductive effort (clutch sizes) were inappropriate given that most of the birds analyzed produce self-feeding precocial offspring, and (iv) the statistical units used in the majority of analyses (species) were not statistically independent with respect to higher level taxonomy. After correcting these problems, I found little evidence of survival–fecundity trade-offs among precocial game birds, and I attribute most of the explainable variation in life-history traits of these birds to allometry, phylogeny, and geography.

scholarly journals Patterns of Life-History Diversification in North American Fishes: implications for Population Regulation

1992 ◽  
Vol 49 (10) ◽  
pp. 2196-2218 ◽  
Author(s):  
Kirk O. Winemiller ◽  
Kenneth A. Rose
Keyword(s):  
Life History ◽  
Parental Care ◽  
North American ◽  
Life Histories ◽  
Egg Size ◽  
Life History Strategies ◽  
Large Species ◽  
High Fecundity ◽  
Adult Growth ◽  
Trade Offs

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.

scholarly journals The influence of juvenile and adult environments on life-history trajectories

2005 ◽  
Vol 273 (1587) ◽  
pp. 741-750 ◽  
Author(s):  
Barbara Taborsky
Keyword(s):  
Life History ◽  
Life Histories ◽  
Adult Life ◽  
Growth Conditions ◽  
Offspring Size ◽  
Juvenile Growth ◽  
Life History Variation ◽  
Major Life ◽  
Adult Growth ◽  
Trade Offs

There is increasing evidence that the environment experienced early in life can strongly influence adult life histories. It is largely unknown, however, how past and present conditions influence suites of life-history traits regarding major life-history trade-offs. Especially in animals with indeterminate growth, we may expect that environmental conditions of juveniles and adults independently or interactively influence the life-history trade-off between growth and reproduction after maturation. Juvenile growth conditions may initiate a feedback loop determining adult allocation patterns, triggered by size-dependent mortality risk. I tested this possibility in a long-term growth experiment with mouthbrooding cichlids. Females were raised either on a high-food or low-food diet. After maturation half of them were switched to the opposite treatment, while the other half remained unchanged. Adult growth was determined by current resource availability, but key reproductive traits like reproductive rate and offspring size were only influenced by juvenile growth conditions, irrespective of the ration received as adults. Moreover, the allocation of resources to growth versus reproduction and to offspring number versus size were shaped by juvenile rather than adult ecology. These results indicate that early individual history must be considered when analysing causes of life-history variation in natural populations.

scholarly journals Foundress Number, But Not Queen Size or Boldness, Predicts Colony Life-History in Wild Paper Wasps

2019 ◽  
Author(s):  
Colin M. Wright ◽  
David N. Fisher ◽  
Wayne V. Nerone ◽  
James L.L. Lichtenstein ◽  
Elizabeth A. Tibbetts ◽  
...  
Keyword(s):  
Resource Allocation ◽  
Life History ◽  
Body Size ◽  
Life Histories ◽  
Life History Traits ◽  
Positive Association ◽  
Paper Wasps ◽  
Trade Offs ◽  
Behavioral Tendencies ◽  
Queen Size

AbstractColonies of social insects exhibit a spectacular variety of life histories. Here we documented the degree of variation in colony life-history traits, mostly related to productivity, in two species of wild paper wasps. We then tested for associations between colony life-history traits to look for trade-offs or positively associated syndromes, and examined whether individual differences in the behavioral tendencies of foundresses (Polistes metricus) or the number of cofoundresses (P. fuscatus) influenced colony life-history. The majority of our measures of colony life-history were positively related, indicating no obvious resource allocation trade-offs. Instead, the positive association of traits into a productivity syndrome appears to be driven by differences in queen or microhabitat quality. Syndrome structure differed only marginally between species. Queen boldness and body size were not associated with colony life-history inP. metricus. Colonies initiated by multipleP. fuscatusfoundresses were generally more productive, and this advantage was approximately proportional to the number of cofoundresses. These findings demonstrate that colony life-history traits can be associated together much like individual life-history traits, and the associations seen here convey that differences in overall productivity drive between-colony differences in life-history.

scholarly journals The metabolic pace of life histories across fishes

2020 ◽  
Author(s):  
Serena Wong ◽  
Jennifer S. Bigman ◽  
Nicholas K. Dulvy
Keyword(s):  
Life History ◽  
Metabolic Rate ◽  
Growth Performance ◽  
Body Mass ◽  
Life Histories ◽  
Life History Traits ◽  
Generation Length ◽  
Pace Of Life ◽  
Trade Offs ◽  
Maximum Body

AbstractAll life acquires energy through metabolic processes and that energy is subsequently allocated to life-sustaining functions such as survival, growth, and reproduction. Thus, it has long been assumed that metabolic rate is related to the life history of an organism. Indeed, metabolic rate is commonly believed to set the pace of life by determining where an organism is situated along a fast-slow life history continuum. However, empirical evidence of a relationship between metabolic rate and life histories is lacking, especially for ectothermic organisms. Here, we ask whether three life history traits – maximum body mass, generation length, and growth performance – explain variation in resting metabolic rate (RMR) across fishes. We found that growth performance, which accounts for the trade-off between growth rate and maximum body size, explained variation in RMR, yet maximum body mass and generation length did not. Our results suggest that measures of life history that encompass trade-offs between life history traits, rather than traits in isolation, explain variation in RMR across fishes. Ultimately, understanding the relationship between metabolic rate and life history is crucial to metabolic ecology and has the potential to improve prediction of the ecological risk of data-poor species.

scholarly journals Marine trophic diversity in an anadromous fish is linked to its life-history variation in fresh water

2013 ◽  
Vol 9 (1) ◽  
pp. 20120824 ◽  
Author(s):  
Susan P. Johnson ◽  
Daniel E. Schindler
Keyword(s):  
Life History ◽  
Life Histories ◽  
Sockeye Salmon ◽  
Freshwater Ecosystems ◽  
Life History Variation ◽  
Trophic Diversity ◽  
Trade Offs ◽  
Salmon Population ◽  
Freshwater Habitats ◽  
Foraging Tactics

We used carbon and nitrogen stable isotopes from muscle tissues accrued in the ocean to examine whether marine foraging tactics in anadromous sockeye salmon ( Oncorhynchus nerka ) are linked to their ultimate freshwater life history as adults. Adults from large-bodied populations spawning in deep freshwater habitats had more enriched δ 15 N than individuals from small-bodied populations from shallow streams. Within populations, earlier maturing individuals had higher δ 15 N than older fish. These differences in δ 15 N suggest that the fish with different life histories or spawning habitats in freshwater either fed at different trophic positions or in different habitats in the ocean. We propose that, nested within interspecific diversity in the ecological attributes of salmon, population and life-history diversity in spawning adults is associated with variation in marine foraging tactics. These results further indicate that the trophic diversity of sockeye salmon in the ocean may be linked to trade-offs in ecological and evolutionary constraints they eventually experience as adults in freshwater ecosystems.

scholarly journals The metabolic pace of life histories across fishes

2021 ◽  
Vol 288 (1953) ◽  
pp. 20210910
Author(s):  
Serena Wong ◽  
Jennifer S. Bigman ◽  
Nicholas K. Dulvy
Keyword(s):  
Life History ◽  
Metabolic Rate ◽  
Growth Performance ◽  
Body Mass ◽  
Life Histories ◽  
Life History Traits ◽  
Generation Length ◽  
Pace Of Life ◽  
Trade Offs ◽  
Maximum Body

All life acquires energy through metabolic processes and that energy is subsequently allocated to life-sustaining functions such as survival, growth and reproduction. Thus, it has long been assumed that metabolic rate is related to the life history of an organism. Indeed, metabolic rate is commonly believed to set the pace of life by determining where an organism is situated along a fast–slow life-history continuum. However, empirical evidence of a direct interspecific relationship between metabolic rate and life histories is lacking, especially for ectothermic organisms. Here, we ask whether three life-history traits—maximum body mass, generation length and growth performance—explain variation in resting metabolic rate (RMR) across fishes. We found that growth performance, which accounts for the trade-off between growth rate and maximum body size, explained variation in RMR, yet maximum body mass and generation length did not. Our results suggest that measures of life history that encompass trade-offs between life-history traits, rather than traits in isolation, explain variation in RMR across fishes. Ultimately, understanding the relationship between metabolic rate and life history is crucial to metabolic ecology and has the potential to improve prediction of the ecological risk of data-poor species.

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