Putative autoimmune reaction of striped bass, Morone saxatilis, to skin and kidney-tubule basement membranes
No abstract available.
Geology topics
Publications and source records attributed to C. A. Lemm.
No abstract available.
We formulated four diets that simulated the amino acid profiles of eggs of striped bass Morone saxatilis , carcasses of larval striped bass, eggs of rainbow trout Oncorhynchus mykiss , or nauplii of Artemia salina ; a fifth diet contained a high concentration (33.6%) of shrimp meal. These diets were fed to juvenile striped bass for 14 weeks. Striped bass grew best when fed diets with an amino acid pattern that simulated the patterns of rainbow trout eggs or Artemia salina . Fish fed these two diets grew as well as, and had carcass compositions and protein efficiency ratios similar to those of, control fish fed the federally specified ASD2‐30 salmon diet. No histological or morphological abnormalities were noted. These two diets, which have potentially lower production costs and contain slightly less protein than ASD2‐30, may be used as prototype diets specifically for striped bass. Through further minor refinements, the diets could be used in production hatcheries.
The nutritional value of Artemia nauplii from the Great Salt Lake was effectively improved for larval striped bass ( Morone saxatilis ) by incorporation of unsaturated fatty acids (20: 5 n -3 and 22: 6 n -3) into the nauplii by the direct method of enrichment. Survival at 24 days post-hatch increased from 23% to 64% when fish were fed nauplii containing 8.24% lipid as 20: 5 n -3 and 3.10% as 22: 6 n -3 fatty acids. Growth of the larval fish was significantly improved by a diet of fatty acid enriched nauplii. Fatty acid composition of the larvae reflected the composition of the fed nauplii. Results suggested a requirement by larval striped bass for long-chain highly unsaturated fatty acids and an inability, at this stage of development, to elongate and desaturate the shorter chain fatty acids in sufficient amounts to meet this requirement.
Benzocaine was tested as an anesthetic on juvenile and mature adult striped bass ( Morone saxatilis ). Concentrations of 55 mg/L at 22°C to 80 mg/L at 11°C effectively anesthetized fish in about 3 min. Recovery was more rapid as temperature increased. Fish survived concentrations of twice the effective concentration and exposure times up to 60 min at the effective concentration. Striped bass required higher concentrations for anesthetization than had been previously demonstrated for salmonid fishes, but safety margins for both concentration and exposure time were wider than for the salmonids.
No abstract available at this time
Six commercially available diets varying in lipid, protein, water, ash, and carbohydrate contents were fed to Atlantic salmon ( Salmo salar ) for 2 years to determine if diet affected smoltification. Each month, from March to September of the second year, sampled fish were exposed to 33‰ seawater for 24 h to determine smolt readiness, defined as the ability to maintain water and salt balance in a seawater challenge. Regardless of diet, Atlantic salmon were able to regulate plasma sodium and chloride ions (smoltify) only during early May. It is unlikely that hatchery managers could effectively use high‐energy diets to control the time of smoltification in Atlantic salmon.
No abstract available at this time
Growth rates of tiger muskellunge (muskellunge Esox masquinongy ♀ x northern pike E. lucius ♂) fed diets containing 35, 45, or 55% crude protein for 5 weeks at 17, 20, or 23°C were compared. Fish fed diets containing 45 or 55% protein grew faster at all temperatures than those fed 35% protein. Growth of tiger muskellunge fed a diet containing either 45 or 55% protein did not increase significantly at optimum growth temperatures (20 or 23°C). At 17°C, below the optimum temperature range, growth did increase when the percentage of protein in the diet was increased.
No abstract available at this time
Underyearling walleyes, allowed to move freely in a Y‐shaped chamber into which various substances were added to one arm or another, were attracted to sodium chloride, sucrose, glutathione, vitamin B 12 , betaine, arginine, Daphnia slurries, some fish slurries, washings from live Daphnia and Artemia, and some commercial fish foods. They avoided cysteine, glycine, glycine‐betaine, Artemia slurries, some fish slurries, and fish mucus; and showed little reaction to valeric and caproic acid, and some commercial fish foods. Tests of visual response, in which beakers containing live food organisms were placed in the arms of the chamber, indicated that walleyes respond strongly to the movement of food organisms. Walleyes usually surrounded the beakers containing live food organisms and repeatedly struck the glass. They were attracted more strongly to Artemia than to Daphnia. Results indicate that odor plays an important role in movement of walleyes to food and that there is a potential for attracting intensively cultured walleyes to man‐made diets with odorants.
Growth and survival were compared for groups of first‐feeding fry of Atlantic salmon (Salmo salar) fed various commercially available and experimental starter diets. In two separate 8‐ to 9‐week studies, survival was highest (more than 90%) in fish fed a semimoist closed‐formula commercial diet (BioDiet). In one study, fish grew fastest on BioDiet, whereas in the second study they grew fastest on a liver‐supplemented diet. Some diets were not eaten by the fish, resulting in little growth and less than 40% survival.