Growth Rate and Body Composition of Fingerling Sockeye Salmon, Oncorhynchus nerka, in relation to Temperature and Ration Size

1969 ◽  
Vol 26 (9) ◽  
pp. 2363-2394 ◽  
Author(s):  
J. R. Brett ◽  
J. E. Shelbourn ◽  
C. T. Shoop
Keyword(s):  
Growth Rate ◽  
Sockeye Salmon ◽  
Oncorhynchus Nerka ◽  
Maximum Growth ◽  
Maximum Growth Rate ◽  
Food Conversion ◽  
Lower Temperature ◽  
Ration Size ◽  
Conversion Efficiencies ◽  
Maintenance Ration

The growth of young sockeye salmon (Oncorhynchus nerka) was studied at temperatures ranging from 1 to 24 C in relation to rations of 0, 1.5, 3, 4.5, and 6% of dry body weight per day, and at an "excess" ration. Optimum growth occurred at approximately 15 C for the two highest rations, shifting progressively to a lower temperature at each lower ration. The maximum growth rate for sockeye 5–7 months old was 2.6%/day; that for fish 7–12 months old was 1.6%/day. At 1 C a ration of 1.5%/day was sufficient to provide for a maximum growth rate of 0.23%/day. The maintenance ration was found to increase rapidly above 12 C, amounting to 2.6%/day at 20 C. No growth took place at approximately 23 C despite the presence of excess food.Isopleths for gross and net food-conversion efficiencies were calculated. A maximum gross efficiency of 25% occurred in a small area with a center at 11.5 C and a ration of 4.0%/day; a maximum net efficiency of 40% occurred within a range of 8–10 C for rations of 1.5%/day down to 0.8%/day, the maintenance level.Gross body constituents changed in response to the imposed conditions, varying in extreme from 86.9% water, 9.4% protein, and 1.0% fat for starved fish at 20 C to 71.3% water, 19.7% protein, and 7.6% fat on an excess ration at 15 C.It is concluded on the basis of growth and food-conversion efficiency that temperatures from 5 to 17 C are most favorable for young sockeye, and that a general physiological optimum occurs in the vicinity of 15 C.

Scope for Metabolism and Growth of Sockeye Salmon, Oncorhynchus nerka, and Some Related Energetics

1976 ◽  
Vol 33 (2) ◽  
pp. 307-313 ◽  
Author(s):  
J. R. Brett
Keyword(s):  
Growth Rate ◽  
Sockeye Salmon ◽  
Oncorhynchus Nerka ◽  
Maximum Growth ◽  
General Concept ◽  
Maximum Growth Rate ◽  
Scope For Growth ◽  
Metabolic Scope ◽  
The Difference

The extent of metabolic and feeding requirements for fingerling sockeye salmon (Oncorhynchus nerka) are compared over the tolerable range of temperature. Scope for growth, derived from the difference between maximum and maintenance rations, is shown to relate to temperature in a manner similar to that for maximum growth rate. Metabolic scope is compared with scope for growth, supporting the general concept of scope for activity developed by Fry (1947).

Effects of Sublethal Concentrations of Sodium Pentachlorophenate on Growth Rate, Food Conversion Efficiency, and Swimming Performance in Underyearling Sockeye Salmon (Oncorhynchus nerka)

1973 ◽  
Vol 30 (4) ◽  
pp. 499-507 ◽  
Author(s):  
P. W. Webb ◽  
J. R. Brett
Keyword(s):  
Growth Rate ◽  
Conversion Efficiency ◽  
Sockeye Salmon ◽  
Swimming Performance ◽  
Oncorhynchus Nerka ◽  
Dry Weight ◽  
Food Conversion ◽  
Ration Level ◽  
Sodium Pentachlorophenate ◽  
Sublethal Concentrations

Tests were performed at 15 C, pH 6.8, and dissolved oxygen values of 90–100% air saturation. Growth rate and conversion efficiency were measured by feeding a ration level of 15% body dry weight/day to underyearling sockeye salmon (Oncorhynchus nerka) held at sodium pentachlorophenate (PCP) concentrations of 0, 1.14, 1.99, 3.49, 7.16, 13.60, 27.73, 31.57, and 47.18 ppb. Swimming performance was measured at PCP concentrations of 0, 7.21, 19.00, and 50.00 ppb. The 96-hr LC50 was 63 ppb PCP. Growth rate and conversion efficiency were almost equally affected by PCP, the EC50 values being 1.74 ppb for growth rate and 1.80 ppb for conversion efficiency. This is approximately 2.8% of the 96-hr LC50. Swimming performance was unaffected by PCP at the concentrations used.

Growth Responses of Young Sockeye Salmon (Oncorhynchus nerka) to Different Diets and Planes of Nutrition

1971 ◽  
Vol 28 (10) ◽  
pp. 1635-1643 ◽  
Author(s):  
J. R. Brett
Keyword(s):  
Conversion Efficiency ◽  
Sockeye Salmon ◽  
Growth Response ◽  
Fish Meal ◽  
Oncorhynchus Nerka ◽  
Maximum Growth ◽  
Test Diet ◽  
Growth Responses ◽  
Marine Zooplankton ◽  
Conversion Efficiencies

The growth rate and food conversion efficiency of yearling sockeye salmon (Oncorhynchus nerka) (26 ± 2 g) was determined for Halver's test diet, Clark's Chinook mash, Abernathy pellets, frozen marine zooplankton, and sockeye mash, using a number of planes of nutrition. The maximum growth rates at 15 C varied from 3.1% dry body wt/day (Halver's) to 1.5%/day (marine zooplankton) with corresponding gross conversion efficiencies of 48 and 10%. Maintenance rations were determined, mostly by extrapolation, and used to evaluate the net conversion efficiency for each diet. The highest was 74% net conversion on Halver's test diet. Although major differences in growth response existed between the five diets, it was concluded that the various moist diets based on fish meal, used in these and earlier experiments, were not significantly different from each other when on the same plane of nutrition.

A note on growth curves of rabbit lines selected on growth rate or litter size

1993 ◽  
Vol 57 (2) ◽  
pp. 332-334 ◽  
Author(s):  
A. Blasco ◽  
E. Gómez
Keyword(s):  
Growth Rate ◽  
Litter Size ◽  
Growth Curves ◽  
Live Weight ◽  
Maximum Growth ◽  
Maximum Growth Rate ◽  
Standard Errors ◽  
Adult Weight ◽  
Weight Growth ◽  
Using Data

Two synthetic lines of rabbits were used in the experiment. Line V, selected on litter size, and line R, selected on growth rate. Ninety-six animals were randomly collected from 48 litters, taking a male and a female each time. Richards and Gompertz growth curves were fitted. Sexual dimorphism appeared in the line V but not in the R. Values for b and k were similar in all curves. Maximum growth rate took place in weeks 7 to 8. A break due to weaning could be observed in weeks 4 to 5. Although there is a remarkable similarity of the values of all the parameters using data from the first 20 weeks only, the higher standard errors on adult weight would make 30 weeks the preferable time to take data for live-weight growth curves.

Reassessment of Maximum Growth Rates for C3 and C4 Crops

1978 ◽  
Vol 14 (1) ◽  
pp. 1-5 ◽  
Author(s):  
J. L. Monteith
Keyword(s):  
Growth Rate ◽  
Growth Rates ◽  
Growing Season ◽  
Maximum Growth ◽  
Maximum Growth Rate ◽  
Crop Growth ◽  
Close Inspection ◽  
Similar Difference ◽  
Photosynthetic Efficiencies

SUMMARYFigures for maximum crop growth rates, reviewed by Gifford (1974), suggest that the productivity of C3 and C4 species is almost indistinguishable. However, close inspection of these figures at source and correspondence with several authors revealed a number of errors. When all unreliable figures were discarded, the maximum growth rate for C3 stands fell in the range 34–39 g m−2 d−1 compared with 50–54 g m−2 d−1 for C4 stands. Maximum growth rates averaged over the whole growing season showed a similar difference: 13 g m−2 d−1 for C3 and 22 g m−2 d−1 for C4. These figures correspond to photosynthetic efficiencies of approximately 1·4 and 2·0%.

Interpretation of Experimental Data with Regard to the Activated Sludge Model No.1 and Calibration of the Model for Municipal Wastewater Treatment Plants

1992 ◽  
Vol 25 (6) ◽  
pp. 167-183 ◽  
Author(s):  
H. Siegrist ◽  
M. Tschui
Keyword(s):  
Experimental Data ◽  
Growth Rate ◽  
Activated Sludge ◽  
Municipal Wastewater ◽  
Wastewater Treatment Plants ◽  
Treatment Plant ◽  
Maximum Growth ◽  
Maximum Growth Rate ◽  
Municipal Wastewater Treatment ◽  
Activated Sludge Model

The wastewater of the municipal treatment plants Zürich-Werdhölzli (350000 population equivalents), Zürich-Glatt (110000), and Wattwil (20000) have been characterized with regard to the activated sludge model Nr.1 of the IAWPRC task group. Zürich-Glatt and Wattwil are partly nitrifying treatment plants and Zürich-Werdhölzli is fully nitrifying. The mixing characteristics of the aeration tanks at Werdhölzli and Glatt were determined with sodium bromide as a tracer. The experimental data were used to calibrate hydrolysis, heterotrophic growth and nitrification. Problems arising by calibrating hydrolysis of the paniculate material and by measuring oxygen consumption of heterotrophic and nitrifying microorganisms are discussed. For hydrolysis the experimental data indicate first-order kinetics. For nitrification a maximum growth rate of 0.40±0.07 d−1, corresponding to an observed growth rate of 0.26±0.04 d−1 was calculated at 10°C. The half velocity constant found for 12 and 20°C was 2 mg NH4-N/l. The calibrated model was verified with experimental dam of me Zürich-Werdhölzli treatment plant during ammonia shock load.

Dietary Protein Requirements of Fishes — A Reassessment

1987 ◽  
Vol 44 (11) ◽  
pp. 1995-2001 ◽  
Author(s):  
Stephen H. Bowen
Keyword(s):  
Growth Rate ◽  
Dietary Protein ◽  
Protein Concentration ◽  
Trophic Ecology ◽  
Maximum Growth ◽  
Maximum Growth Rate ◽  
Intake Rate ◽  
Protein Requirement ◽  
Fish Physiology ◽  
Protein Retention

It is widely believed that fishes require more dietary protein than other vertebrates. Many aspects of fish physiology, nutrition, and trophic ecology have been interpreted within the context of this high protein requirement. Here, fishes are compared with terrestrial homeotherms in terms of (1) protein requirement for maintenance, (2) relative protein concentration in the diet required for maximum growth rate, (3) protein intake rate required for maximum growth rate, (4) efficiency of protein retention in growth, and (5) weight of growth achieved per weight of protein ingested. The two animal groups compared differ only in relative protein concentration in the diet required for maximum growth rate. This difference is explained in terms of homeotherms' greater requirement for energy and does not reflect absolute differences in protein requirement. The remaining measures of protein requirement suggest that fishes and terrestrial homeotherms are remarkably similar in their use of protein as a nutritional resource. Reinterpretation of the role of protein in fish physiology, nutrition, and trophic ecology is perhaps in order.

Allometric scaling and taxonomic variation in nutrient utilization traits and maximum growth rate of phytoplankton

2012 ◽  
Vol 57 (2) ◽  
pp. 554-566 ◽  
Author(s):  
Kyle F. Edwards ◽  
Mridul K. Thomas ◽  
Christopher A. Klausmeier ◽  
Elena Litchman
Keyword(s):  
Growth Rate ◽  
Allometric Scaling ◽  
Maximum Growth ◽  
Nutrient Utilization ◽  
Maximum Growth Rate

Instability waves on the air–sea interface

1993 ◽  
Vol 248 ◽  
pp. 363-381 ◽  
Author(s):  
G. H. Wheless ◽  
G. T. Csanady
Keyword(s):  
Surface Tension ◽  
Growth Rate ◽  
Maximum Growth ◽  
Maximum Growth Rate ◽  
Surface Velocity ◽  
Instability Waves ◽  
Interface Surface ◽  
Fluid Properties ◽  
Compound Matrix Method ◽  
Order Of Magnitude

We used a compound matrix method to integrate the Orr–Sommerfeld equation in an investigation of short instability waves (λ < 6 cm) on the coupled shear flow at the air–sea interface under suddenly imposed wind (a gust model). The method is robust and fast, so that the effects of external variables on growth rate could easily be explored. As expected from past theoretical studies, the growth rate proved sensitive to air and water viscosity, and to the curvature of the air velocity profile very close to the interface. Surface tension had less influence, growth rate increasing somewhat with decreasing surface tension. Maximum growth rate and minimum wave speed nearly coincided for some combinations of fluid properties, but not for others.The most important new finding is that, contrary to some past order of magnitude estimates made on theoretical grounds, the eigenfunctions at these short wavelengths are confined to a distance of the order of the viscous wave boundary-layer thickness from the interface. Correspondingly, the perturbation vorticity is high, the streamwise surface velocity perturbation in typical cases being five times the orbital velocity of free waves on an undisturbed water surface. The instability waves should therefore be thought of as fundamentally different flow structures from free waves: given their high vorticity, they are akin to incipient turbulent eddies. They may also be expected to break at a much lower steepness than free waves.

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