Evolutionary assembly rules for fish life histories

By E. Charnov, H. Gislason, J. Pope. 2013

179 citations recorded by the source corpus.

Subfields: Ecology, Global and Planetary Change, Nature and Landscape Conservation

View Paper: https://www.semanticscholar.org/paper/38df383fab4314466a7e21c996c00f817dbad586

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In Ecology

In Global and Planetary Change

In Nature and Landscape Conservation

Citations in the corpus

Revisiting the concept of Beverton -Holt life-history invariants with the aim of informing data-poor fisheries assessment (2015, background): “This is unlikely to be true in nature, as juvenile mortality rates are generally observed to be greater than adult mortality rates, and mortality rates maybe size-related throughout a species’ life cycle (Gislasson et al., 2010; Charnov et al., 2013).”
Is oxygen limitation in warming waters a valid mechanism to explain decreased body sizes in aquatic ectotherms? (2018, background): “Such a negative 603 correlation is indeed observed across a range of taxa, and at least in fish has been formalised 604 as one of the life-history invariants (Charnov et al., 2013).”
Energy acquisition and allocation to egg production in relation to fish reproductive strategies (2014, background): “The heritability of these traits, where measured, may be quite low (Ware 1984; Roff 2002; Brown et al. 2008; Charnov et al. 2013; McBride in press).”
Natural mortality estimators for information‐limited fisheries (2014, methodology): “More recently, Charnov et al. (2012) have argued that Mt at tm typically equals 1.82 K for fish and reptiles that have growth patterns which can be adequately described by the von Bertalanffy function, though they did not propose that as an estimator. As Charnov et al. (2012) sawM declining with age”
A simple length-structured model based on life history ratios and incorporating size-dependent selectivity: application to spawning potential ratios for data-poor stocks (2016, background): “However, there is evidence that natural mortality is 141 higher for smaller individuals, and tends to decrease as the animals grow to larger sizes (with 142 a possible increase again towards the end of life; Charnov et al. 2013, Charnov 2014).”
Trends and management implications of human-influenced life-history changes in marine ectotherms (2016, background): “In the evolutionary and physiological 200 interpretation of the VB growth model presented by Charnov et al. (2013), L∞ or maximum body size, is 201 determined by both food availability and/or changes in maintenance and reproduction, whereas k, or rly 202 growth rate, is affected only by the…”
From traits to life‐history strategies: Deconstructing fish community composition across European seas (2017, background): “They are 80 often based on a theoretical framework and are used to shed light on the evolution of the life history of 81 organisms, as well as the environment wherein the species occur (Charnov et al. 2013).”