1997
DOI: 10.1006/jmsc.1996.0200
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Temporal and geographic variation in maturity at length and age of Greenland halibut (Reinhardtius hippoglossoides) from the Canadian north-west Atlantic with implications for fisheries management

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Cited by 33 publications
(27 citation statements)
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“…For example, the mean length-atmaturity (14.9 cm TL) in our study in the north-western Mediterranean was much lower than those reported for warmer water populations inhabiting the Canarian Archipelago (18.3 cm TL) (Pajuelo et al, 2003b) and the Gulf of Tunisia (15.33-16.13 cm TL) (Chakroun-Marzouk & Ktari, 2006;Fehri-bedoui & Gharbi, 2008). The size-atmaturity of fish is known to vary spatially and temporally and is usually closely related to total population abundance over the life of a cohort, with cohorts maturing at a smaller size when population size is low (Rijnsdorp, 1993;Morgan & Bowering, 1997;Morgan & Colbourne, 1999). Furthermore, water temperature has been assumed to affect only body growth and so the effects of temperature on maturation and reproductive effort appear to be indirect via the optimization of life-history traits in fish populations (Charnov & Gillooly, 2004).…”
Section: Discussionmentioning
confidence: 99%
“…For example, the mean length-atmaturity (14.9 cm TL) in our study in the north-western Mediterranean was much lower than those reported for warmer water populations inhabiting the Canarian Archipelago (18.3 cm TL) (Pajuelo et al, 2003b) and the Gulf of Tunisia (15.33-16.13 cm TL) (Chakroun-Marzouk & Ktari, 2006;Fehri-bedoui & Gharbi, 2008). The size-atmaturity of fish is known to vary spatially and temporally and is usually closely related to total population abundance over the life of a cohort, with cohorts maturing at a smaller size when population size is low (Rijnsdorp, 1993;Morgan & Bowering, 1997;Morgan & Colbourne, 1999). Furthermore, water temperature has been assumed to affect only body growth and so the effects of temperature on maturation and reproductive effort appear to be indirect via the optimization of life-history traits in fish populations (Charnov & Gillooly, 2004).…”
Section: Discussionmentioning
confidence: 99%
“…typical snapshot studies). Indeed, a lack of information of levels of variability in demographic parameters (including rates of growth and mortality) across a species distribution could confound biological-based fisheries assessments and management plans (Morgan & Bowering 1997, Ruttenberg et al 2005, Jakobsen et al 2009). …”
Section: Maturity and Fishery Considerationsmentioning
confidence: 99%
“…11). There were very few catches of Greenland halibut at depths less than 200 m. Most of the Greenland halibut caught on the Flemish Cap were immature because few fish were larger than 60 cm (Alpoim et al, MS 2002), the lower end of the range of L 50 values reported for females sampled near the Cap (Morgan and Bowering, 1997).…”
Section: Collocation Of Cod and Plaicementioning
confidence: 99%
“…In both summer and winter, plaice are most abundant at depths of 100 to 200 m on the northern Grand Banks (Morgan and Brodie, 1991). Although plaice have been found in the deeper waters of the Flemish Pass (Iglesias journal.nafo.int et al, 1996), there is no evidence of mixing between the Flemish Cap and Grand Banks populations (Morgan and Bowering MS, 2004). The summer depth distributions of cod populations located within the general latitudinal range of the Flemish Cap tend to be shallow.…”
Section: Introductionmentioning
confidence: 99%