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Cod Larvae (cod + larva)
Selected AbstractsEffects of ontogeny, temperature, and light on vertical movements of larval Pacific cod (Gadus macrocephalus)FISHERIES OCEANOGRAPHY, Issue 5 2009THOMAS P. HURST Abstract The role of behavior, especially vertical migration, is recognized as a critical component of realistic models of larval fish dispersion. Unfortunately, our understanding of these behaviors lags well behind our ability to construct three-dimensional flow-field models. Previous field studies of vertical behavior of larval Pacific cod (Gadus macrocephalus) were limited to small, preflexion stages (,11 mm SL) in a narrow range of thermal conditions. To develop a more complete picture of larval behavior, we examined the effects of ontogeny, temperature, and light on vertical responses of larval Pacific cod in experimental columns. While eggs were strictly demersal, yolk-sac larvae displayed a strong surface orientation as early as 1 day post hatch (, 5 mm SL). Consistent with field observations, small preflexion larvae (<10 mm SL) showed no response to varying light levels. However, there was a direct effect of temperature on larval behavior: Pacific cod larvae exhibited a stronger surface orientation at 4°C than at 8°C. The behavior of larger, postflexion larvae (>15 mm SL) in experimental columns was consistent with a diel vertical migration and independent of water temperature: fish were more widely distributed in the column, and median positions were consistently deeper at higher light levels. These laboratory observations are combined with observations from discrete-depth (MOCNESS) sampling in the Gulf of Alaska to characterize the vertical distribution of larval Pacific cod and contrast ontogenetic patterns with walleye pollock (Theragra chalcogramma). The vertical movements of larval Pacific cod described here will be applied in the development of dispersal projections from Gulf of Alaska spawning grounds. [source] Spatial distribution and feeding habits of Pacific cod (Gadus macrocephalus) larvae in Mutsu Bay, JapanFISHERIES OCEANOGRAPHY, Issue 2 2002Tetsuya Takatsu The spatial distributions and feeding habits of Pacific cod (Gadus macrocephalus) larvae, and the spatial distributions of copepod nauplii and copepodites, their main prey, were examined in Mutsu Bay from February to March during 1989,92. Yolk-sac larvae were caught at 30,45 m depth at the bay mouth. Larvae without yolk were collected at 8,45 m depth at the bay mouth and the inner part of the bay, and large larvae were chiefly found in the bay. This geographical pattern in larval size may have been because of transport to the inner part of Mutsu Bay by the Tsugaru Warm Current. The dominant taxa of copepod nauplii and copepodites in the diet and the environment changed each year. Larvae fed mainly on abundant taxa in the environment, suggesting that larvae are opportunistic feeders. Nauplii and copepodites were abundant in the bay, especially in 1992. Copepodites were slightly more abundant in the diet of cod larvae in 1992 than in 1991, but this difference was smaller than in the environment. In addition, larvae with empty digestive tracts were scarce in 1991 and 1992. Prey concentrations in the bay in 1991 and 1992 seem to have been high enough to sustain most Pacific cod larvae. [source] Effects of temperature on larval fish swimming performance: the importance of physics to physiologyJOURNAL OF FISH BIOLOGY, Issue 4 2002I. Hunt von Herbing Temperature influences both the physiology offish larvae and the physics of the flow conditions under which they swim. For small larvae in low Reynolds number (Re) hydrodynamic environments dominated by frictional drag, temperature-induced changes in the physics of water flow have the greatest effect on swimming performance. For larger larvae, in higher Re environments, temperature-induced changes in physiology become more important as larvae swim faster and changes in swimming patterns and mechanics occur. Physiological rates at different temperatures have been quantified using Q10s with the assumption that temperature only affected physiological variables. Consequently, Q10s that did not consider temperature-induced changes in viscosity overestimated the effect of temperature on physiology by 58% and 56% in cold-water herring and cod larvae respectively. In contrast, in warm-water Danube bleak larvae, Q10s overestimated temperature-induced effects on physiology by only 5,7%. This may be because in warm water, temperature-induced changes affect viscosity to a smaller degree than in cold water. Temperature also affects muscle contractility and efficiency and at high swimming velocities, efficiency decreases more rapidly in cold-exposed than in warm-exposed muscle fibres. Further experiments are needed to determine whether temperature acts differently on swimming metabolism in different thermal environments. While hydrodynamic factors appear to be very important to larval fish swimming performance in cold water, they appear to lose importance in warm water where temperature effects on physiology dominate. This may suggest that major differences exist among locomotory capacities of larval fish that inhabit cold, temperate waters compared to those that live in warm tropical waters. It is possible that fish larvae may have developed strategies that affect dispersal and recruitment in different aquatic habitats in order to cope not only with temperature-induced physiological challenges, but physical challenges as well. [source] Comparison of dietary phospholipids and neutral lipids: effects on gut, liver and pancreas histology in Atlantic cod (Gadus morha L.) larvaeAQUACULTURE NUTRITION, Issue 1 2009P.-A. WOLD Abstract The aim of the present study was to compare effects of dietary n-3 highly unsaturated fatty acids (HUFA) being incorporated in the phospholipid (PL) or in the neutral lipid (NL) fraction of the larval feed, on larval growth and histology of digestive organs in Atlantic cod (Gadus morhua L.) larvae. Three isoproteic and isolipidic diets, labelled according to the percentage of n-3 docosahexaenoic acid and eicosapentaenoic acid contained in NL1 or in PL1 and PL3 of the diets, were fed to cod larvae from 17 days post hatching (dph) to 45 dph. In the liver, hepatocytes and their nuclei were smaller in NL1 larvae compared with the PL larvae; the mitochondrial membrane structures were less dense and the amount of lipids observed in the liver was significantly higher in NL1 larvae compared with the PL3 larvae. The liver and gut size was related to larval size, with no differences between the larval groups. The results demonstrated that the essential fatty acids were more beneficial for cod larvae when they were incorporated in the dietary polar PL rather than in the NL, and that the n-3 HUFA requirements in cod larvae is possibly higher than that in the PL1 diet. [source] A comparison among differently enriched rotifers (Brachionus plicatilis) and their effect on Atlantic cod (Gadus morhua) larvae early growth, survival and lipid compositionAQUACULTURE NUTRITION, Issue 1 2008A.S. GARCIA Abstract We evaluated the effect of differently enriched rotifers on the early growth, survival and lipid composition of Atlantic cod larvae (Gadus morhua). The enrichments tested were: (i) AlgaMac 2000®; (ii) AquaGrow® Advantage; and (iii) a combination of Pavlova sp. paste and AlgaMac 2000®. Larvae from treatment 3 [1.50 ± 0.11 mg dry weight (dw) and 7.10 ± 0.14 dw specific growth rate (SGR)] were heavier (P = 0.006) and grew faster (P = 0.004) than larvae from treatment 2 (1.03 ± 0.04 mg dw and 6.29 ± 0.04 dw SGR). No significant differences were found in the final weight and SGR among larvae from treatment 1 (1.21 ± 0.07 mg dw and 6.58 ± 0.20 dw SGR) and larvae from treatments 2 and 3. The treatment 3 also resulted in the best survival at the end of the experimental period, estimated to be 3 on a scale from 1 to 5, whereas the survival estimates for the two other groups were 1,2. Larvae from the treatment 3 reached 37 days posthatch with levels of ,6DPA 32-fold higher than newly hatched larvae. Differences in the larval enrichment of ,6DPA may explain the differences in growth and survival of the Atlantic cod larvae. [source] Vertebral deformity in cultured Atlantic cod larvae: ontogeny and effects on mortalityAQUACULTURE RESEARCH, Issue 14 2009Velmurugu Puvanendran Abstract The effects of different egg incubation densities on the incidences of vertebral deformities in Atlantic cod larvae were investigated. Cod eggs were incubated at four different densities, 3, 6, 12 and 48 mL eggs L,1, of water. When all the eggs hatched, larvae were reared in 30 L glass aquaria. Larval samples were taken at 0, 14, 42 and 56 days post hatch (dph) for deformity analysis. Larval samples were stained using bone and cartilage staining methods to determine vertebral deformity. Incubation densities did not have any significant effects on vertebral deformities in Atlantic cod larvae. However, the incidence of larval vertebral deformity was high at hatch and decreased as the larvae grew older until 42 dph, indicating selective mortality of deformed larvae during this period. Larvae at 56 dph, however, showed an increase in the incidence of vertebral deformity, indicating a possible nutritional or prey-type effect. To our knowledge, no studies have documented the occurrence of variable patterns in vertebral deformities in cod at various developmental stages. Overall, our results suggest that broodstock husbandry, genetics and/or nutrition could play a major role in causing vertebral deformities in Atlantic cod at hatch; however, nutrition and prey type may play a major role during metamorphosis. [source] | ||||||||||