MATERNAL AGE AS A DETERMINANT OF LARVAL GROWTH AND SURVIVAL IN A MARINE FISH, SEBASTES MELANOPS

By S. Berkeley, Colin G. Chapman, S. Sogard. 2004

749 citations recorded by the source corpus.

Subfields: Aquatic Science, Global and Planetary Change, Nature and Landscape Conservation

View Paper: https://www.semanticscholar.org/paper/fe6ac0fffa6a2d6f44cf5689a0411a08daebdf11

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In Aquatic Science

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Citations in the corpus

Shifting dynamic forces in fish stock fluctuations triggered by age truncation? (2011, background): “Furthermore, older and larger fish have been demonstrated to produce larger eggs (Chambers & Waiwood, 1996; Berkeley et al., 2004), leading to increased survival of eggs and yolk-sac larvae (Nissling et al., 1998).”
Assessing changes in age and size at maturation in collapsing populations of Atlantic cod (Gadus morhua) (2005, neutral): “As pointed out by Berkeley et al. (2004b) Fig.”
The non-linear relationship between body size and function in parrotfishes (2008, background): “Reduction in mean body size may undermine the reproductive capacity of Wsh populations by reducing fecundity (Love and Johnson 1999; Evans et al. 2008), diminishing the quality of Wsh larvae (Berkeley et al. 2004), and altering sex-ratio relationships (Petersen and Warner 2002).”
Changes in spawning stock structure strengthen the link between climate and recruitment in a heavily fished cod (Gadus morhua) stock (2006, background): “In particular, populations located near the extremes of the geographical range of the species may depend on irregular recruitment occurring mainly during periods of favourable climatic conditions (MacCall, 1996; Berkeley et al., 2004).”
Conservation and fisheries effects of spawning aggregation marine protected areas: What we know, where we should go, and what we need to get there (2014, background): “, 1996; Sadovy, 1996) and potentially indirectly because of a positive relationship between egg quality and body size as reported in some fish species (Berkeley et al., 2004).”
Extreme genetic diversity and temporal rather than spatial partitioning in a widely distributed coral reef fish (2007, methodology): “Finally, the generation time for N. vlamingii was calculated using the formula T =( + )/2, where is the age at Wrst reproduction and is the age at last reproduction (Pianka 1978) and assumes that Wsh are reproductively active throughout this period (e.g. Berkeley et al. 2004; Pears et al. 2006).”
Rethinking length-based fisheries regulations: the value of protecting old and large fish with harvest slots (2015, background): “Our simulations did not account for size-dependent maternal effects on offspring performance as demonstrated previously for a range of species (e.g. Berkeley et al. 2004b; Venturelli et al. 2009; Arlinghaus et al. 2010) and therefore likely produced predictions of harvest and catch lower than would…”
The application of genetics to marine management and conservation: Examples from the Indo-Pacific (2014, background): “Likewise, larger females produce exponentially more, and often bigger, eggs that develop up to three times faster and survive starvation for more than twice as long as larvae produced by smaller females (Berkeley et al. 2004, Birkeland and Dayton 2005).”
Paradigm shifts in marine fisheries genetics: ugly hypotheses slain by beautiful facts (2008, background): “1996; Zeldis and Francis 1998), but also potentially more viable eggs and larvae (Berkeley et al. 2004; Fisher et al. 2007; Sogard et al. 2008).”
Fisheries Sustainability via Protection of Age Structure and Spatial Distribution of Fish Populations (2004, background): “The mechanism appears to be the volume of the larval oil globule at birth, which is strongly related to maternal age (Berkeley et al. 2004).”