Home About us Contact
|
Home About us Contact | ||
|
|
||
Large Pelagic Fishes (large + pelagic_fish)
Selected AbstractsSchooling and migration of large pelagic fishes relative to environmental cuesFISHERIES OCEANOGRAPHY, Issue 2 2000Robert Humston A kinesis model driven by high-resolution sea surface temperature maps is used to simulate Atlantic bluefin tuna movements in the Gulf of Maine during summer months. Simulations showed that individuals concentrated in areas of thermal preference. Results are compared to empirical distribution maps of bluefin tuna schools determined from aerial overflights of the stock during the same time periods. Simulations and empirical observations showed similar bluefin tuna distributions along fronts, although interannual variations in temperature ranges occupied suggest that additional foraging factors are involved. Performance of the model is further tested by simulating the relatively large-scale annual north,south migrations of bluefin tuna that followed a preferred thermal regime. Despite the model's relatively simple structure, results suggest that kinesis is an effective mechanism for describing movements of large pelagic fish in the expansive ocean environment. [source] Evaluating the physiological and physical consequences of capture on post-release survivorship in large pelagic fishesFISHERIES MANAGEMENT & ECOLOGY, Issue 2 2007G. B. SKOMAL Abstract, Sharks, tunas and billfishes are fished extensively throughout the world. Domestic and international management measures (quotas, minimum sizes, bag limits) mandate release of a large, yet poorly quantified, number of these fishes annually. Post-release survivorship is difficult to evaluate, because standard methods are not applicable to large oceanic fishes. This paper presents information on the current approaches to characterising capture stress and survivorship in sharks, tunas and marlins. To assess mortality associated with capture stress, researchers must examine the cumulative impacts of physical trauma and physiological stress. Physical trauma, manifested as external and internal tissue and organ damage, is caused by fishing gear and handling. Gross examination and histopathological sampling have been used to assess physical trauma and to infer post-release survivorship. Exhaustive anaerobic muscular activity and time out of water cause physiological stress, which has been quantified in these fishes through the analyses of blood chemistry. Conventional, acoustic and archival tagging have been used to assess post-release survivorship in these species. Future studies relating capture stress and post-release survivorship could yield information that helps fishermen increase survivorship when practicing catch and release. [source] Schooling and migration of large pelagic fishes relative to environmental cuesFISHERIES OCEANOGRAPHY, Issue 2 2000Robert Humston A kinesis model driven by high-resolution sea surface temperature maps is used to simulate Atlantic bluefin tuna movements in the Gulf of Maine during summer months. Simulations showed that individuals concentrated in areas of thermal preference. Results are compared to empirical distribution maps of bluefin tuna schools determined from aerial overflights of the stock during the same time periods. Simulations and empirical observations showed similar bluefin tuna distributions along fronts, although interannual variations in temperature ranges occupied suggest that additional foraging factors are involved. Performance of the model is further tested by simulating the relatively large-scale annual north,south migrations of bluefin tuna that followed a preferred thermal regime. Despite the model's relatively simple structure, results suggest that kinesis is an effective mechanism for describing movements of large pelagic fish in the expansive ocean environment. [source] Variation in the diet of the Patagonian toothfish with size, depth and season around the Falkland IslandsJOURNAL OF FISH BIOLOGY, Issue 2 2003A. Arkhipkin The ontogenetic and seasonal variations in the feeding spectrum were studied in 756 specimens of the Patagonian toothfish Dissostichus eleginoides (16,159 cm total length, LT) collected on the shelf, continental slope and bathyal waters (67,1960 m, depth range) around the Falkland Islands between April 1999 and August 2002. On the shelf, small toothfish (<40 cm LT) were active predators taking mostly one relatively large prey item at a time (mainly near-bottom Patagonotothen ramsayi and Loligo gahi). Medium-size toothfish (40,60 cm LT) fed on the same prey, but the number of prey items increased to 1,2 items per fish. Large toothfish (>60 cm LT) switched their diet to other large pelagic fishes occurring near the bottom (Macruronus magellanicus and Micromesistius australis australis), again taking mostly one prey item at a time. The diet of medium-size D. eleginoides on the shelf varied seasonally depending on the abundance and migrations of the major prey species. Patagonotothen ramsayi was abundant in the diet throughout the year, whereas L. gahi appeared only from February to October during its offshore seasonal migrations to the depth range of D. eleginoides. During November to January, L. gahi migrated inshore to spawn and disappeared from the toothfish diet, being substituted by M. australis australis which dispersed on the shelf after spawning. After its ontogenetic descent to the lower part of the continental slope (500,1000 m depths), toothfish took less active (than on the shelf) fishes such as Antimora rostrata whilst also feeding on active near-bottom macrourids and skates. In their deepest habitat (>1000 m depths), toothfish became a typical opportunistic predator, feeding mainly on relatively small and inactive fishes, squids and prawn-like crustaceans Acanthephyra pelagica and Thymops birsteini. Decrease in hunting activity with depth could be related to a specific adaptation to keep neutral buoyancy by increase of lipid content in white muscles of D. eleginoides with size. [source] | ||||||||||