Effects of habitat on settlement, growth, and postsettlement survival of Atlantic cod (Gadus morhua)

1995 ◽  
Vol 52 (9) ◽  
pp. 1834-1841 ◽  
Author(s):  
M. Tupper ◽  
R. G. Boutilier

Settlement and growth of age 0+ cod were monitored using snorkel and self-contained underwater breathing apparatus (SCUBA) in four distinct habitat types (sand, seagrass, cobble, and rock reef) in St. Margaret's Bay, Nova Scotia. Newly settled cod were marked with acrylic dye, allowing repeated visual length estimates of individual fish. Settlement of cod did not differ between habitat types, but postsettlement survival and subsequent juvenile densities were higher in more structurally complex habitats. These differences appear to be due to increased shelter availability and decreased predator efficiency in structurally complex habitats. Growth rate was highest in seagrass beds, while the efficiency of cod predators was lowest and cod survival was highest on rocky reefs and cobble bottoms. Thus, trade-offs occur between energy gain and predation risk. In St. Margaret's Bay, the population structure of Atlantic cod may be less influenced by patterns of larval supply than by postsettlement processes such as habitat-specific growth and mortality.


2010 ◽  
Vol 67 (5) ◽  
pp. 866-876 ◽  
Author(s):  
Marion Harrald ◽  
Peter J. Wright ◽  
Francis C. Neat

The North Sea stock of Atlantic cod ( Gadus morhua ) is comprised of a number of subcomponents that differ both genetically and phenotypically. A potential cause for such spatial variability is adaptive divergence, which may be linked to differences in thermal environment and (or) historical fishing pressure. Here we present evidence that spatial variation in maturity–size relationships in the wild has a significant intrinsic component. Using a common-environment experiment on wild-caught juveniles raised through to maturity, we demonstrate that cod from the southern North Sea (SNS) mature at larger sizes than those from the northwestern North Sea (NWNS) despite broadly similar growth rates. Consistent with these experimental results, year-class-specific maturity ogives for recent maturing year classes (1999–2001) suggested that the length at which 50% of females reached maturity was 11 cm greater for SNS than for NWNS cod. Under a common environment, smaller female size at maturity partly reflected higher relative liver weight, with NWNS females having a higher relative liver weight than SNS females. By investigating maturation under controlled conditions, our study provides evidence for life history trade-offs in energy allocation between growth, energy storage, and reproduction that may underlie the spatial variation observed in the field.



2007 ◽  
Vol 64 (12) ◽  
pp. 1747-1760 ◽  
Author(s):  
Espen Strand ◽  
Geir Huse

We investigate the trade-offs associated with vertical migration and swimming speed of Atlantic cod (Gadus morhua) using an adaptive individual-based model. Simulations with varying distribution and occurrence of prey, with and without swimbladder constraints, and visual predation were performed. Most simulations resulted in cod migrations between the bottom and pelagic zones. In simulations with high probability of encountering pelagic prey, the cod spent the daytime in the pelagic zone, moving to the bottom to feed only when no pelagic prey were encountered. At night the cod stayed in the pelagic zone to attain neutral buoyancy. In simulations with low occurrence of pelagic prey or high visual predation pressure, the cod remained at the bottom feeding on the consistently present benthic prey. If the pelagic prey occurred far above the sea floor or there were no benthic prey, the cod abandoned all bottom contact. The study thus predicts that the probability of encountering energy-rich pelagic prey is the key factor in driving vertical migration in adult cod. Buoyancy regulation is further shown to be an important constraint on vertical migration.



2014 ◽  
Vol 71 (7) ◽  
pp. 1106-1112 ◽  
Author(s):  
Arild Folkvord ◽  
Christian Jørgensen ◽  
Knut Korsbrekke ◽  
Richard D.M. Nash ◽  
Trygve Nilsen ◽  
...  

Animals partition and trade off their resources between competing needs such as growth, maintenance, and reproduction. Over a lifetime, allocation strategies should result in distinct trajectories for growth, survival, and reproduction, but such longitudinal individual data are difficult to reconstruct for wild animals and especially marine fish. We were able to reconstruct two of these trajectories in wild-caught Northeast Arctic cod (Gadus morhua) females: size-at-age was back-calculated from otolith growth increments, and recent spawning history was reconstructed from postovulatory follicles and present oocyte development. Our findings indicate distinct trade-offs between length growth and reproduction. Fish that sexually matured early had attained a larger size at age 3 than immatures, but onset of reproduction caused slower growth compared with immatures. We found that 6- and 7-year-old females skipping spawning grew significantly more in the year of missed spawning than females spawning for the second consecutive year. The latter tentatively supports the hypothesis that skipped spawning may occur as an adaptive life-history strategy, given the potential future fecundity gain with increased size.



2004 ◽  
Vol 61 (6) ◽  
pp. 983-991 ◽  
Author(s):  
Björn Björnsson ◽  
Maria Álvaro Dongala Dombaxe

Abstract Nephrops was found to be of low quality as food for cod. In a laboratory experiment the mean specific growth rate of 1 kg cod was 0.184 and 0.415% d−1 when fed to satiation on Nephrops and capelin, respectively. This large difference in growth rate resulted not only from less intake of Nephrops (1.19 kg cod−1) than capelin (1.55 kg cod−1) but also because more Nephrops (4.6 kg) than capelin (2.2 kg) were required to produce each kilogramme of cod. Higher food conversion ratio was consistent with lower fat content of Nephrops (1.3%) than capelin (9.2%) but the exoskeleton also reduced the digestion rate of Nephrops. In the groups where Nephrops and capelin of equal mean weight were offered simultaneously, 40% of the diet consisted of Nephrops during the first week and 10% during the final seven weeks of the experiment. At the end of the experiment, condition factor, liver index, and gonadosomatic index were significantly lower for cod fed on Nephrops (0.967, 5.7, 7.1, respectively) than for those fed on capelin (1.086, 15.8, 11.2, respectively). These results suggests that predation by cod on Nephrops might be reduced by regular release of capelin or other similar food in the distributional areas of Nephrops.



2015 ◽  
Vol 11 (2) ◽  
pp. 20141032 ◽  
Author(s):  
Rebecca E. Holt ◽  
Christian Jørgensen

The difference between maximum metabolic rate and standard metabolic rate is referred to as aerobic scope, and because it constrains performance it is suggested to constitute a key limiting process prescribing how fish may cope with or adapt to climate warming. We use an evolutionary bioenergetics model for Atlantic cod ( Gadus morhua ) to predict optimal life histories and behaviours at different temperatures. The model assumes common trade-offs and predicts that optimal temperatures for growth and fitness lie below that for aerobic scope; aerobic scope is thus a poor predictor of fitness at high temperatures. Initially, warming expands aerobic scope, allowing for faster growth and increased reproduction. Beyond the optimal temperature for fitness, increased metabolic requirements intensify foraging and reduce survival; oxygen budgeting conflicts thus constrain successful completion of the life cycle. The model illustrates how physiological adaptations are part of a suite of traits that have coevolved.



2012 ◽  
Vol 466 ◽  
pp. 215-223 ◽  
Author(s):  
P Ljungberg ◽  
PA Nilsson ◽  
A Persson


2021 ◽  
Vol 12 (3-2021) ◽  
pp. 13-19
Author(s):  
O.V. Bondarev ◽  

In this article presented data on the growth of the atlantic cod Gadus morhua Linnaeus, 1758 and pollock Pollachius virens (Linnaeus, 1758) juveniles in Zelenetskaya Bay in 2018. The daily specific growth rate and production rate were calculated. The length of atlantic cod juveniles in July–September varied from 3.5 to 7.9 cm, and pollock – from 2.5 to 9.4 cm. The daily specific weight growth rate (qw) of atlantic cod juveniles in Zelenetskaya Bay from July to August was 0.41, and from August to September – 1.08; for pollock juveniles, these indicators are 1.32 and 0.94, respectively. The daily specific production (C) of atlantic cod juveniles in Zelenetskaya Bay over the summer period varied from 0.015 to 0.036, and of pollock juveniles – from 0.011 to 0.042.



2016 ◽  
Vol 73 (3) ◽  
pp. 349-357 ◽  
Author(s):  
Christopher M. Legault ◽  
Michael C. Palmer

Traditionally, the natural mortality rate (M) in a stock assessment is assumed to be constant. When M increases within an assessment, the question arises how to change the fishing mortality rate target (FTarget). Per recruit considerations lead to an increase in FTarget, while limiting total mortality leads to a decrease in FTarget. Application of either approach can result in nonsensical results. Short-term gains in yield associated with high FTarget values should be considered in light of potential losses in future yield if the high total mortality rate leads to a decrease in recruitment. Examples using yellowtail flounder (Limanda ferruginea) and Atlantic cod (Gadus morhua) are used to demonstrate that FTarget can change when M increases within an assessment and to illustrate the consequences of different FTarget values. When a change in M within an assessment is contemplated, first consider the amount and strength of empirical evidence to support the change. When the empirical evidence is not strong, we recommend using a constant M. If strong empirical evidence exists, we recommend estimating FTarget for a range of stock–recruitment relationships and evaluating the trade-offs between risk of overfishing and forgone yield.



1999 ◽  
Vol 56 (11) ◽  
pp. 2099-2111 ◽  
Author(s):  
Erling Otterlei ◽  
Gunnar Nyhammer ◽  
Arild Folkvord ◽  
Sigurd O Stefansson

Norwegian coastal (NC) and northeast Arctic (NA) Atlantic cod (Gadus morhua) larvae were reared on live zooplankton to investigate temperature- and size-specific growth. Larval and juvenile growth was temperature and size dependent. Growth in length and weight increased with increasing temperature from 4 to 14°C, with a corresponding reduced larval stage duration. Maximum growth rate occurred at a larval size of 0.1-1.0 mg dry weight, followed by a declining trend during the juvenile stage. The temperature optimum of larval cod fed in excess is estimated to be between 14 and 16°C, with a maximum weight-specific growth potential exceeding 25%·day-1. Temperature- and stock-specific growth curves of dry weight at age are well described by a generalized Gompertz model. A stock-specific difference in mean weight at age was observed, with NC growing better than NA. Neither countergradient latitudinal variation in growth capacity of the two larval cod stocks nor temperature adaptation across latitudes was indicated. A stock-specific difference in weight at length was observed in early juveniles, with NC being heavier than NA. Overall, a positive correlation between temperature and condition level was found. No distinct temperature- or stock-specific differences in survival were observed.



2006 ◽  
Vol 63 (2) ◽  
pp. 235-245 ◽  
Author(s):  
K.E. Jørstad ◽  
Ø. Karlsen ◽  
T. Svåsand ◽  
H. Otterå

Abstract A major aim of the aquaculture industry in Norway is to develop sustainable farming of Atlantic cod, Gadus morhua L. A great deal of research, including farming trials and stock enhancement, has been performed on this species in Norway during the past two decades. The success of domestication of a new species depends on the genetic variability of the wild broodstock and the selection of appropriate genotypes for the farming environment. Growth experiments under farmed conditions, including genetic analyses, were started as early as 1983 after the breakthrough of cod juvenile production in mesocosm systems. At later stages (1988 and 1992 year classes), more detailed studies were conducted under farmed conditions. Based on individual tagging and genotyping (blood and white muscle biopsy sampling), estimates of growth performance (specific growth rate, SGR) of the various genotypes within six polymorphic protein loci were obtained. In general, the SGR in the two experiments varied through the year as a function of temperature and body size. In the 1988 year-class experiment, only a few statistically significant differences (ANOVA) were detected among genotypes, measured as mean weight and SGR. The 1992 year-class experiment included two different cod stocks, Northeast Arctic (NE) and Norwegian coastal (NC) cod, which were reared for about two years in the same net pen. Further, during this experiment, only a few genotypes exhibited significantly different growth within the NE group. No consistency was found in the variation with regard to protein loci investigated, growth periods studied, and relationship with temperature variation.



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