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Michaela Aschan Randi Ingvaldsen 《Deep Sea Research Part II: Topical Studies in Oceanography》2009,56(21-22):2012
The shrimp spawn in autumn, and the females carry their eggs as out roe until spring when the larvae hatch. Within a period of 2 months the shrimp larvae settle to the bottom. It has been claimed that the year-class strength probably is determined during the larval phase. Today's assessment and forecast of the shrimp stock productivity and potential fishing yields are weak. This is partly due to poor knowledge on population dynamics from hatching until the shrimp are caught in the fishery at the age of 3 or 4 years. We, therefore, here identify the most important abiotic and biotic factors that affect recruitment in addition to spawning stock biomass. Since 1995, a net attached to the underbelly of the survey trawl used at the annual cruise in the Barents Sea has caught juvenile shrimp. The abundance of settled shrimp larvae varies in time and space. The recruitment to the fishery has been quite stable with the exception of the 1996 year-class, which was observed as 1-year-olds but has not been registered since. The temporal pattern of the three youngest year-classes is studied in relation to abiotic factors such as sea temperature, ice index and North Atlantic Oscillation, as well as biotic factors such as spawning stock biomass and presence of copepods, euphausiids and predating cod. Recruitment indices and factors identified by the Spearmann correlation to be significantly correlated with recruitment were used as input in a principal component analysis (PCA) and a generalized additive model (GAM) was applied. Abundance of 1-year-old shrimp is positively correlated to spawning stock biomass the previous year and to temperature of the previous winter, and negatively correlated with the number of 1-year-old cod. Two-year-old shrimp show significant correlation with temperature, whereas there is a strong negative correlation with euphausiids. Three-year-old shrimp are significantly correlated with the number of 2-year-old shrimp the previous year but negatively correlated to temperature at sampling time. This is probably due to less overlap with the main predator cod when cold. Ricker functions indicate an increased density-dependent mortality with age. When predicting the recruitment of shrimp to the fishery, the spawning stock biomass, the abundance of cod and euphausiids, as well as the temperature should be included. 相似文献
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Einar M. Nilssen Michaela M. Aschan 《Deep Sea Research Part II: Topical Studies in Oceanography》2009,56(21-22):2023
The Jan Mayen area has an extreme environment with low temperatures and infrequent, but abrupt temperature changes. The shrimp population here is considered to be on its edge of distribution. The life-history parameters are in the same range as in other high-latitude shrimp populations and are characterized by slow growth, large size at maturation and extended longevity. Irregular and sporadic commercial exploitation limit fishing mortality and give the population life-history parameters not previously seen in other areas. The Jan Mayen shrimp are large compared to, e.g., the Barents Sea shrimp and can reach a maximum carapace length (Lmax) of 37 mm and an age of 10–11 years. The large size at sex transformation (L50, >24 mm) and analyses of length–frequency distributions indicate that the shrimp may be 6–7 years of age before changing sex. The change in Lmax and L50 observed during the study period is probably caused by increased natural mortality due to sudden temperature changes or due to increased predation, rather than increased growth rates. The life-history strategy of shrimp in the Jan Mayen area can be explained by factors such as depth, temperature and population density variations caused by fluctuation in recruitment and mortality.The shrimp fisheries in the Jan Mayen area began in the late 1970s and reached an annual landing of 2000 tonnes in 1985, and since then landings have oscillated around 500 tonnes depending on a combination of factors. The survey indices of stock biomass varied between 3000 and 6600 tonnes. For most years, the highest shrimp densities are at a depth of 200–299 m, while large shrimp (and therefore also female shrimp) are dominant at depths greater than 300 m.Fish community data were studied as the composition of the demersal fish community is an integrated response to environmental conditions and as predation affects the shrimp stock. Polar cod and capelin are the most abundant fish species in the study area. A high number of blue whiting was registered in 1979, but the number declined in 1980 and 1981 as temperature decreased. During the surveys in 1994 and 1995, no blue whiting was registered. A few individuals were found again in the 1999 samples. The number of Greenland halibut has declined from the beginning of the 1980s to the 1990s. 相似文献
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Renée Katrin Bechmann Bodil Katrine Larsen Ingrid Christina Taban Per Møller 《Marine pollution bulletin》2010,60(11):2087-2098
Adult shrimps (Pandalus borealis) and their embryos were exposed to an oil-water dispersion (OWD) at concentrations of 0.015, 0.06 and 0.25 mg/L using a continuous flow system. Lysosomal membrane stability was analysed in haemocytes using the neutral red retention assay and an alkaline unwinding assay was used to measure DNA damage in hepatopancreas tissue. Exposure to oil induced concentration and time dependent biomarker responses in adult shrimps together with the accumulation of PAH in their tissues. Oil exposure of shrimp embryos caused increased mortality in the resultant larvae, even if the larvae were kept in clean water after hatching. There were minor differences observed in larval stage development times in the first part of the experiments. The fatty acid composition of embryos exposed to oil was different to that of non-exposed larvae. PAH tissue concentration and biomarker responses correlated to the reduced survival of the shrimp larvae. 相似文献
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