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.

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 Population declines of tuna and relatives depend on their speed of life

2015 ◽  
Vol 282 (1811) ◽  
pp. 20150322 ◽  
Author(s):  
M. J. Juan-Jordá ◽  
I. Mosqueira ◽  
J. Freire ◽  
N. K. Dulvy
Keyword(s):  
Life History ◽  
Life Histories ◽  
Life History Traits ◽  
Population Level ◽  
Maximum Size ◽  
Latitudinal Gradients ◽  
Fishing Mortality ◽  
Population Declines ◽  
Wide Range ◽  
Exploitation Status

Larger-bodied species in a wide range of taxonomic groups including mammals, fishes and birds tend to decline more steeply and are at greater risk of extinction. Yet, the diversity in life histories is governed not only by body size, but also by time-related traits. A key question is whether this size-dependency of vulnerability also holds, not just locally, but globally across a wider range of environments. We test the relative importance of size- and time-related life-history traits and fishing mortality in determining population declines and current exploitation status in tunas and their relatives. We use high-quality datasets of half a century of population trajectories combined with population-level fishing mortalities and life-history traits. Time-related traits (e.g. growth rate), rather than size-related traits (e.g. maximum size), better explain the extent and rate of declines and current exploitation status across tuna assemblages, after controlling for fishing mortality. Consequently, there is strong geographical patterning in population declines, such that populations with slower life histories (found at higher cooler latitudes) have declined most and more steeply and have a higher probability of being overfished than populations with faster life histories (found at tropical latitudes). Hence, the strong, temperature-driven, latitudinal gradients in life-history traits may underlie the global patterning of population declines, fisheries collapses and local extinctions.

Fast and slow life histories of carnivores

2011 ◽  
Vol 89 (8) ◽  
pp. 692-704 ◽  
Author(s):  
Evi Paemelaere ◽  
F. Stephen Dobson
Keyword(s):  
Life History ◽  
Body Size ◽  
Litter Size ◽  
Life Histories ◽  
Life History Traits ◽  
Life Cycles ◽  
Age At Maturity ◽  
Negatively Associated ◽  
Trade Offs ◽  
Body Sizes

The fast–slow continuum hypothesis explains life-history traits as reflecting the causal influence of mortality patterns in interaction with trade-offs among traits, particularly more reproductive effort at a cost of shorter lives. Variation among species of different body sizes produce more or less rapid life cycles (respectively, from small to large species), but the fast–slow continuum remains for birds and mammals when body-size effects are statistically removed. We tested for a fast–slow continuum in mammalian carnivores. We found the above trade-offs initially supported in a sample of 85 species. Body size, however, was strongly associated with phylogeny (ρ = 0.79), and thus we used regression techniques and independent contrasts to make statistical adjustments for both. After adjustments, the life-history trade-offs were not apparent, and few associations of life-history traits were significant. Litter size was negatively associated with age at maturity, but slightly positively associated with offspring mass. Litter size and mass were negatively associated with the length of the developmental period. Gestation length showed weak but significant negative associations with age at maturity and longevity. We conclude that carnivores, despite their wide range of body sizes and variable life histories, at best poorly exhibited a fast–slow continuum.

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 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 Linking the performance of a data-limited empirical catch rule to life-history traits

2020 ◽  
Vol 77 (5) ◽  
pp. 1914-1926
Author(s):  
Simon H Fischer ◽  
José A A De Oliveira ◽  
Laurence T Kell
Keyword(s):  
Time Series ◽  
Life History ◽  
Life Histories ◽  
Life History Traits ◽  
Growth Parameter ◽  
Reference Points ◽  
Total Allowable Catch ◽  
Fish Stocks ◽  
Wide Range ◽  
Spawning Stock

Abstract Worldwide, the majorities of fish stocks are data-limited and lack fully quantitative stock assessments. Within ICES, such data-limited stocks are currently managed by setting total allowable catch without the use of target reference points. To ensure that such advice is precautionary, we used management strategy evaluation to evaluate an empirical rule that bases catch advice on recent catches, information from a biomass survey index, catch length frequencies, and MSY reference point proxies. Twenty-nine fish stocks were simulated covering a wide range of life histories. The performance of the rule varied substantially between stocks, and the risk of breaching limit reference points was inversely correlated to the von Bertalanffy growth parameter k. Stocks with k>0.32 year−1 had a high probability of stock collapse. A time series cluster analysis revealed four types of dynamics, i.e. groups with similar terminal spawning stock biomass (collapsed, BMSY, 2BMSY, 3BMSY). It was shown that a single generic catch rule cannot be applied across all life histories, and management should instead be linked to life-history traits, and in particular, the nature of the time series of stock metrics. The lessons learnt can help future work to shape scientific research into data-limited fisheries management and to ensure that fisheries are MSY compliant and precautionary.

Egg production in adult trematodes: adaptation or constraint?

Parasitology ◽  
1997 ◽  
Vol 114 (2) ◽  
pp. 195-204 ◽  
Author(s):  
R. POULIN
Keyword(s):  
Life History ◽  
Body Size ◽  
Life Histories ◽  
Egg Production ◽  
Egg Size ◽  
Life History Traits ◽  
Sampling Site ◽  
Consistent Difference ◽  
Host Body Mass ◽  
Trematode Parasites

Parasite life-history traits should reflect past environmental and host-related selective pressures acting to produce strategies that maximize transmission success. The evolution of adult body size and egg production in 804 species of trematode parasites was investigated using independent contrasts derived from a phylogeny of trematodes. Contrasts in trematode body size were positively correlated with contrasts in egg size, and almost significantly correlated with contrasts in numbers of uterine eggs. After controlling for body size, no relationship existed between egg size and egg numbers, suggesting that there is no trade-off between the two components of egg production. Average host body mass and latitude of the sampling site did not correlate with either trematode body size or egg size. Contrasts between trematode taxa exploiting ectotherm hosts and their sister taxa exploiting endotherms showed no consistent difference in either body size or egg size. The effect of other variables on trematode life-histories, such as the nature of the habitat in which eggs are released, the site of attachment within the host's body, or the number of hosts involved in the life-cycle, could not be evaluated statistically. The similarity in life-history traits among members of given clades suggests that phylogenetic constraints may have acted to limit or mask any adaptive changes expected from changes in host-related or environmental conditions.

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.

scholarly journals Within-host competition drives energy allocation trade-offs in an insect parasitoid

PeerJ ◽  
2020 ◽  
Vol 8 ◽  
pp. e8810
Author(s):  
J. Keaton Wilson ◽  
Laura Ruiz ◽  
Goggy Davidowitz
Keyword(s):  
Life History ◽  
Body Size ◽  
Life History Theory ◽  
Large Body ◽  
Ecological Impacts ◽  
Life History Strategies ◽  
Biological Organization ◽  
Trade Offs ◽  
Wide Range ◽  
Body Sizes

Organismal body size is an important biological trait that has broad impacts across scales of biological organization, from cells to ecosystems. Size is also deeply embedded in life history theory, as the size of an individual is one factor that governs the amount of available resources an individual is able to allocate to different structures and systems. A large body of work examining resource allocation across body sizes (allometry) has demonstrated patterns of allocation to different organismal systems and morphologies, and extrapolated rules governing biological structure and organization. However, the full scope of evolutionary and ecological ramifications of these patterns have yet to be realized. Here, we show that density-dependent larval competition in a natural population of insect parasitoids (Drino rhoeo: Tachinidae) results in a wide range of body sizes (largest flies are more than six times larger (by mass) than the smallest flies). We describe strong patterns of trade-offs between different body structures linked to dispersal and reproduction that point to life history strategies that differ between both males and females and individuals of different sizes. By better understanding the mechanisms that generate natural variation in body size and subsequent effects on the evolution of life history strategies, we gain better insight into the evolutionary and ecological impacts of insect parasitoids in tri-trophic systems.

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