Marine fish life history strategies: applications to fishery management

By J. King, G. A. McFarlane. 2003

340 citations recorded by the source corpus.

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

View Paper: https://www.semanticscholar.org/paper/53c746f797ba5f43dccbe6fd385a63b4fd1d6a1c

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In Ecology

In Global and Planetary Change

In Nature and Landscape Conservation

Citations in the corpus

REPORT OF THE STUDY GROUP ON FISHERIES AND ECOSYSTEM RESPONSES TO RECENT REGIME SHIFTS (2005, background): “These life history strategies range from short-lived, highly variable stock dynamics, which respond immediately to changes in their environment, to extremely long-lived species whose population dynamics are mainly stable (King and McFarlane 2003).”
Life-history strategies predict fish invasions and extirpations in the colorado river basin (2006, background): “…primary life-history strategies that represent the endpoints of a triangular continuum arising from trade-offs among the three basic demographic parameters of survival, fecundity, and onset and duration of reproduction (e.g., Winemiller 1989, Vila-Gispert et al. 2002, King and McFarlane 2003).”
Krill, climate, and contrasting future scenarios for Arctic and Antarctic fisheries (2014, background): “Such conceptual management scenarios based on life-history traits may be particularly useful for newly exploited species (King and McFarlane, 2003; Doyle and Mier, 2012).”
Life history trait diversity of native freshwater fishes in North America (2010, background): “…fish assemblages provide a basis to develop predictive models to help conserve native species and create riskassessment protocols for non-native fishes based on generalised population dynamics and responses to environmental conditions (King & McFarlane 2003; Winemiller 2005; Welcomme et al. 2006).”
Larval fish abundance and physical forcing in the Gulf of Alaska, 1981–2003 (2009, background): “…recognized that life history traits are fundamental to the mechanistic links between environmental change and recruitment (Winemiller and Rose, 1992; Spencer and Collie, 1997; King and McFarlane, 2003, 2006; Conover et al., 2005; Field and Ralston, 2005; Shuter and Abrams, 2005; Winemiller, 2005).”
Is it good or bad to fish with FADs? What are the real impacts of the use of drifting FADs on pelagic marine ecosystems? (2013, background): “Because they have slow growth, late maturation, low fecundity and long reproductive cycles, sharks in general (and silky and oceanic white tip sharks in particular) are among the least resilient of fish species to intense exploitation (Musick et al. 2000; King and McFarlane 2003).”
The Theoretical Biologist's Toolbox: Quantitative Methods for Ecology and Evolutionary Biology (2006, background): “She is speaking about the use of words; the concept is more general. Almost everyone reading this book will be interested in applying mathematics to a problem in the natural world. Skorokhod et al. (2002) describe the difference between pure and applied mathematics as this: ‘‘This book has its roots”
Fast versus slow growing tuna species: age, growth, and implications for population dynamics and fisheries management (2017, background): “…status for the large majority of fish species is unknown or poorly known (Costello et al. 2012), exploitation scenarios using knowledge of fish life histories and their relative sensitivities to fishing pressure provide a starting framework to management (King and McFarlane 2003; Winemiller 2005).”
Comparative analysis of reproductive traits in 65 freshwater fish species: application to the domestication of new fish species (2009, methodology): “For example, the average temperature for larval development (trait 10) of Ictalurus punctatus was used for the unknown developmental temperature of Ameiurus nebulosus larvae, as carried out in similar studies (King and McFarlane 2003).”
Revisiting the concept of Beverton -Holt life-history invariants with the aim of informing data-poor fisheries assessment (2015, methodology): “…cycle, continue growing relatively rapidly as they reproduce, have unfished populations that are dominated by juvenile size classes, and do not exhibit a modal adult size, are opportunist and intermediate strategists (King and McFarlane, 2003) and tend towards being “r-strategists” (Pianka, 1970).”
DNA-based identification of Alaska skates (Amblyraja, Bathyraja and Raja: Rajidae) using cytochrome c oxidase subunit I (coI) variation (2006, background): “Like many elasmobranch fishes, skates appear to be ‘equilibrium’ life-history strategists (Winemiller & Rose, 1992), exhibiting very low intrinsic rates of growth, and sustainable yields in fisheries can be achieved only at very low-to-moderate fishing mortality rates (King & McFarlane, 2003).”
Integrating physiology and life history to improve fisheries management and conservation (2006, background): “Life history and phenotypic adaptations to natural and anthropogenic stressors have been studied in fish systems for many years (Alm 1959; Adams 1980; Thorpe 1990; Winemiller and Rose 1992; McCann and Shuter 1997; Jennings et al. 1998; Johannes 1998; Pope et al. 2000; Rochet 2000; King and McFarlane”
Large‐scale intraspecific variation in life‐history traits of European freshwater fish (2006, background): “…of fish population traits have aimed to classify fish strategies at the species level (Winemiller & Rose, 1992; Vila-Gispert & Moreno-Amich, 2002; King & McFarlane, 2003) and eventually to relate species traits to their latitudinal position (Gotelli & Pyron, 1991; Vila-Gispert et al., 2002).”
Valuable but vulnerable: Over-fishing and under-management continue to threaten groupers so what now? (2020, background): “Within this context, many of the species of groupers within threatened categories are best described as periodic [52] or episodic strategists [53] based on their large body size, slow growth, late maturity, and long-lifespan (e.”