scholarly journals Regional changes in vertebra morphology during ontogeny reflect the life history of Atlantic cod (Gadus morhua L.)

2013 ◽  
Vol 222 (6) ◽  
pp. 615-624 ◽  
Author(s):  
Per G. Fjelldal ◽  
Geir K. Totland ◽  
Tom Hansen ◽  
Harald Kryvi ◽  
Xiyuan Wang ◽  
...  

1960 ◽  
Vol 17 (6) ◽  
pp. 763-774 ◽  
Author(s):  
D. M. Scott ◽  
W. F. Black

Larvae of the parasitic ascarid (Porrocaecum decipiens) occurred commonly in the musculature and viscera of Atlantic cod (Gadus morhua) in the Bras d'Or Lakes. They were also present in the musculature of nine other species of teleosts and probably also in the viscera of skates (Raja sp.). Most larvae were longer than 20 mm. None was shorter than 10 mm, a fact which suggested the existence of some earlier intermediate host, probably an invertebrate. More than 8,000 mysids, an important food of fishes when they first become infected, were examined for nematodes. Although 110 nematodes were found, only one certainly and four dubiously appeared to be Porrocaecum. The definitive hosts were the harbour seal (Phoca vitulina) and the grey seal (Halichoerus grypus). The distribution of seals coincided with local variations in the incidence of the parasite in cod.



2014 ◽  
Vol 514 ◽  
pp. 217-229 ◽  
Author(s):  
HY Wang ◽  
LW Botsford ◽  
JW White ◽  
MJ Fogarty ◽  
F Juanes ◽  
...  


2014 ◽  
Vol 71 (1) ◽  
pp. 151-161 ◽  
Author(s):  
Paul D. Spencer ◽  
Sarah B.M. Kraak ◽  
Edward A. Trippel

Increased larval viability with increased spawner age (i.e., maternal effects) have been observed in Atlantic cod (Gadus morhua) and Pacific rockfish (Sebastes spp.) stocks. Analytical results from a Beverton–Holt recruitment model indicate density-independent maternal effects affected the relative stock productivity and fishing rate reference points. We simulated populations based on Pacific cod (Gadus macrocephalus) and Pacific ocean perch (Sebastes alutus) to explore how estimates of reference points Fmsy and Fcrash are affected by maternal effects and potential interactions with life-history pattern, recruitment autocorrelation, and exploitation rate. Estimates of Fmsy and Fcrash were made from populations with maternal effects using either total larvae (proportional to eggs) or viable larvae (incorporating the maternal effect). Maternal effects have the largest impact upon estimated population productivity at high fishing rates. Estimates of Fmsy and Fcrash for cod were also affected by autocorrelated recruitment variability because of their reduced longevity compared with Pacific ocean perch. These results suggest the importance of evaluating the influence of maternal effects on estimated stock productivity on a case-by-case basis, particularly for depleted stocks composed of relatively young spawners.





2006 ◽  
Vol 63 (2) ◽  
pp. 216-223 ◽  
Author(s):  
Håkon Otterå ◽  
Ann-Lisbeth Agnalt ◽  
Knut E. Jørstad

Abstract Several hundred Atlantic cod (Gadus morhua L.) were collected from selected spawning grounds along the Norwegian coast in March 2002. Four areas or regions that represent a wide range of environmental conditions were chosen for our breeding experiments: Porsangerfjord, Tysfjord, Helgeland, and Øygarden. Cod were transported to Øygarden near Bergen, individually tagged, and kept in sea cages. In both 2003 and 2004, a total of 40 family groups (adult pairs) representing the four regions were monitored for their spawning performance in separate tanks. During the spawning period, the quantity and diameter of eggs were recorded. During 2003, the time of peak spawning differed among groups. It was evident that the broodstock from the Øygarden region spawned about one month earlier than the broodstock collected from the Helgeland region. This also occurred in 2004, two years after the cod were collected, suggesting that the difference has a genetic component. Differences in life history parameters between cod populations, such as spawning cycles as described here, could be adaptive and under genetic control. This must be taken into consideration when assessing precautionary means of overcoming the problem with escapees from future cod mariculture.



1994 ◽  
Vol 51 (12) ◽  
pp. 2834-2842 ◽  
Author(s):  
Sally V. Goddard ◽  
J. S. Wroblewski ◽  
C. T. Taggart ◽  
K. A. Howse ◽  
W. L. Bailey ◽  
...  

Adult Atlantic cod (Gadus morhua) are known to produce antifreeze glycoproteins in response to cold temperatures. Our laboratory studies demonstrated that blood plasma levels in adult cod were positively correlated with the number of days they spent in subzero water. Between April 1991 and June 1993, we monitored concentrations of antifreeze glycoproteins in the plasma of late juvenile and adult cod in Trinity Bay, Newfoundland, and used the results to estimate how long cod had been exposed to low water temperatures. A consideration of these data in conjunction with detailed temperature profiles of the area taken over the course of the study allowed us to deduce the distribution of cod in relation to the temperature field. This study provides evidence that (1) blood antifreeze glycoprotein levels can be used to deduce the recent thermal history of cod in the wild and (2) after their inshore summer feeding period, considerable numbers of adult cod overwintered inshore in Trinity Bay in subzero water, producing antifreeze glycoproteins as temperatures fell below 0 °C. From May onwards, "cold-adapted" cod moved into warming surface waters, where they became available to an early inshore trap fishery.



2013 ◽  
Vol 29 (3) ◽  
pp. 623-629 ◽  
Author(s):  
M.-M. Kroll ◽  
M. A. Peck ◽  
I. A. E. Butts ◽  
E. A. Trippel


2005 ◽  
Vol 62 (4) ◽  
pp. 824-832 ◽  
Author(s):  
Jeffrey A Hutchings

Changes to life history traits are often concomitant with prolonged periods of exploitation. In the Northwest Atlantic, 30- to 40-year declines of more than 90% of Atlantic cod (Gadus morhua) have been associated with significant reductions in age and length at maturity, changes most parsimoniously explained as genetic responses to fishing. Increased survival costs of reproduction associated with earlier maturity, resulting in higher natural mortality and shorter life span, negatively affect population growth rate and rate of recovery. Coupled with lower hatching rate among first-time spawners and smaller size at maturity, a modest reduction in age from 6 to 4 years can reduce annual population growth in Atlantic cod by 25%–30%, based on the output of a stochastic, age-structured life history model. Earlier maturity more than doubles the probability of negative population growth every generation. These results underscore the potential for fishing-induced changes to life history traits alone to generate slow or negligible recovery in marine fishes, exacerbating negative impacts on population growth resulting from ecosystem-level alterations to interspecific competition and predation.



2014 ◽  
Vol 281 (1777) ◽  
pp. 20132976 ◽  
Author(s):  
Guðbjörg Ásta Ólafsdóttir ◽  
Kristen M. Westfall ◽  
Ragnar Edvardsson ◽  
Snæbjörn Pálsson

Atlantic cod ( Gadus morhua ) vertebrae from archaeological sites were used to study the history of the Icelandic Atlantic cod population in the time period of 1500–1990. Specifically, we used coalescence modelling to estimate population size and fluctuations from the sequence diversity at the cytochrome b ( cytb ) and Pantophysin I ( Pan I) loci. The models are consistent with an expanding population during the warm medieval period, large historical effective population size ( N E ), a marked bottleneck event at 1400–1500 and a decrease in N E in early modern times. The model results are corroborated by the reduction of haplotype and nucleotide variation over time and pairwise population distance as a significant portion of nucleotide variation partitioned across the 1550 time mark. The mean age of the historical fished stock is high in medieval times with a truncation in age in early modern times. The population size crash coincides with a period of known cooling in the North Atlantic, and we conclude that the collapse may be related to climate or climate-induced ecosystem change.



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