Energetics of Sablefish, Anoplopoma fimbria, under Laboratory Conditions

1982 ◽  
Vol 39 (7) ◽  
pp. 1012-1020 ◽  
Author(s):  
Kathleen M. Sullivan ◽  
Kenneth L. Smith Jr.
Keyword(s):  
Body Weight ◽  
Oxygen Consumption ◽  
Growth Rates ◽  
The Body ◽  
Fish Growth ◽  
Metabolic Rates ◽  
Anoplopoma Fimbria ◽  
Consumption Rates ◽  
Excretion Rates ◽  
Conversion Efficiencies

We measured respiration, growth, ingestion, and excretion rates for sablefish, Anoplopoma fimbria, collected off southern California at a depth of 500 m and maintained in the laboratory. We also measured the water, protein, and lipid content of white skeletal muscle in both laboratory-held and field fish. Sablefish fed a large ration (14% of wet body weight) every 7–10 d showed growth rates two to three times higher than known growth rates for field fish. On a reduced ration (4% of wet body weight) sablefish grew at rates similar to field fish, but white muscle composition varied significantly from field fish. Oxygen consumption rates under constant temperature conditions showed a decrease in the weight-specific oxygen consumption rates with increase in body weight, ranging from routine metabolic rates of 195.8 mg O2∙kg−1∙h−1 for a 0.25-kg fish to 60.8 mg O2∙kg−1∙h−1 for a 2.78-kg fish. Based on measurements of respiration and excretion, sablefish were estimated to have 162 d of energy stored in the body lipids and did not show signs of starvation stress with food deprivation up to 6 mo in the laboratory. Energy allocation shows very slow growth rates, low conversion efficiencies, and low metabolic rates as adjustments made to large, infrequent meals.Key words: physiological responses, benthopelagic fish, growth, metabolic rate, respiration, excretion

Effect of Growth Rate on Mineral Retention and Body Composition of Growing Lambs

1988 ◽  
Vol 1988 ◽  
pp. 102-102 ◽  
Author(s):  
M Wan Zahari ◽  
J K Thompson ◽  
D Scott
Keyword(s):  
Growth Rate ◽  
Body Composition ◽  
Body Weight ◽  
Calcium Carbonate ◽  
Growth Rates ◽  
Fast Rate ◽  
Basal Diet ◽  
Primary Objective ◽  
The Body ◽  
Secondary Objective

The effects of plane of nutrition on the body composition of growing sheep are very apparent when animals are compared at the same age following different nutritional histories. These differences are, however, less obvious when animals of the same breed and sex are compared at the same body weight and at present there is some conjecture whether composition is affected by growth rate. This uncertainty is not limited to fat and protein but includes the bone and ash, fraction and the ash composition.The primary objective of this trial was to study the effects of different growth rates achieved by feeding different amounts of the same concentrate diet on the composition of empty-body gain and on the retention of minerals by growing lambs. A secondary objective was to examine the effect of adding supplementary calcium carbonate to the basal diet at the fast rate of growth.

The relationship between cirral activity and oxygen uptake in Balanus balanoides

1965 ◽  
Vol 45 (2) ◽  
pp. 387-403 ◽  
Author(s):  
R. C. Newell ◽  
H. R. Northcroft
Keyword(s):  
Body Weight ◽  
Oxygen Consumption ◽  
Oxygen Uptake ◽  
Mantle Cavity ◽  
The Body ◽  
Effect Of Temperature ◽  
Zero Rate ◽  
Rate Of Oxygen Consumption ◽  
The Relationship ◽  
Balanus Balanoides

The rate of cirral beat of Balanus balanoides is related to the logarithm of the body weight as an exponential function. In any one animal, there is little effect of temperature on cirral activity between 7·5° and 10° C. Between 10° and 20° C, however, there is a rapid increase in cirral beat with temperature followed by a fall at temperatures above 20° C.Balanus balanoides exhibits a fast, medium and zero rate of oxygen consumption. These rates of oxygen consumption correspond with (a) normal cirral beating, (b) ‘testing’ activity with no cirral movement, and (c) with the closure of the mantle cavity. Both of the possible levels of oxygen uptake are related to the logarithm of the body weight in a logarithmic fashion over the temperature range 7·5°–22·5° C. Temperature affects the two rates of oxygen consumption differently. In the slower rate (rate B) there is an increase in the rate of oxygen consumption between 7·5° and 14° C but there is no significant increase in the rate of oxygen consumption between 14° and 22·5 C°.

scholarly journals 127 Dietary supplementation with glycine improves the post-weaning growth of low-birth-weight pigs

2019 ◽  
Vol 97 (Supplement_3) ◽  
pp. 112-112
Author(s):  
Wenliang He ◽  
Erin A Posey ◽  
Guoyao Wu
Keyword(s):  
Body Weight ◽  
Birth Weight ◽  
Growth Rates ◽  
Corn Starch ◽  
Low Cost ◽  
Dietary Supplementation ◽  
Experimental Period ◽  
The Body ◽  
Economic Returns ◽  
On Farm

Abstract Pigs with intrauterine growth restriction (IUGR) represent 20–25% of all pigs born and are culled on farm, resulting in enormous losses. This study tested the hypothesis that dietary supplementation with glycine enhanced the growth of IUGR pigs after weaning. Healthy pigs [14 IUGR pigs (birth weight = 0.98±0.03 kg, mean ± SEM) and 20 NBW pigs (birth weight = 1.44±0.02 kg, mean ± SEM)] were used for the trial. At weaning (21 d of age), pigs within each birth weight group were assigned randomly into corn- and soybean meal-based diets supplemented with 1% glycine plus 0.19% corn starch or 1.19% alanine (isonitrogenous control). There were 7 IUGR pigs and 10 NBW pigs per subgroup. Crude protein content in basal diets was 20% between d 21 and 64, 18% between d 65 and 108, and 16% between d 109 and 120 of age. During the 100-d period of feeding, feed intake per kg body weight did not differ (P > 0.05) between IUGR and NBW pigs or between control and glycine groups. Growth rates of NBW pigs supplemented with 1% glycine did not differ (P > 0.05) from those for NBW pigs without glycine supplementation. In contrast, growth rates of IUGR pigs supplemented with 1% glycine were 28%, 15%, and 10% greater (P > 0.05) than those for IUGR pigs without glycine supplementation during d 21–35, d 35–64, and d 65–120 of age, respectively. Growth rates of NBW pigs were greater (P > 0.05) than those for IUGR pigs without glycine supplementation during any experimental period. By d 120 of age, the body weight of IUGR pigs with glycine supplementation did not differ (P > 0.05) from that of NBW pigs. Collectively, our results indicate that dietary supplementation with 1% glycine (a low-cost supplement) beneficially improves their growth rate and economic returns. Supported by a USDA/NIFA grant.

The metabolic rates of newborn pigs in relation to floor insulation and ambient temperature

1971 ◽  
Vol 13 (2) ◽  
pp. 303-313 ◽  
Author(s):  
D. B. Stephens
Keyword(s):  
Body Weight ◽  
Oxygen Consumption ◽  
Ambient Temperature ◽  
Regression Coefficients ◽  
Metabolic Rates ◽  
Similar Treatment ◽  
Concrete Floor ◽  
Ambient Temperatures ◽  
Newborn Pigs ◽  
Floor Material

SUMMARY1. The metabolic rates of 58 individual piglets kept either on a straw or on a concrete floor at ambient temperatures near to 10°, 20° or 30°C have been measured with ages ranging from newborn to 9 days, and body weight from 1·0 to 3·2 kg. The oxygen consumption was measured on each floor material at the chosen ambient temperature thus allowing paired comparisons for each animal.2. In comparison with the concrete floor, oxygen consumption on straw was reduced by 18% at 10°C, 27% at 20°C and by 12% at 30°C for pigs 2 to 9 days old. The regression coefficients of mean log (oxygen consumption) on log (body weight) were around 0·66 at 10° and 20°C. At 30°C the value was 0·99 ± 0·14. The regression coefficients were not significantly affected by the presence of a straw floor showing that its effect did not vary with body weight. Corresponding values foi piglets below 24 hours of age were 17% at 10°C, 27% at 20°C and 22% at 30°C ambient temperature.3. Moving a piglet on to a straw floor at 10°C had the same thermal effect as raising the ambient temperature to 18°C. Similar treatment at 30°C was equivalent to raising the ambient temperature to 32°C.4. Lowering ambient temperature to increase the temperature gradient between the homeothermic body of the piglet and the environment progressively increased heat loss in all cases. There was a concomitant decrease in the calculated conductance between core and environment which was more pronounced for the piglets lying on the concrete floor.

SEASONAL ACCLIMATIZATION IN WILD RATS (RATUS NORVEGICUS)

1963 ◽  
Vol 41 (5) ◽  
pp. 711-716 ◽  
Author(s):  
J. S. Hart ◽  
O. Heroux
Keyword(s):  
Body Weight ◽  
Oxygen Consumption ◽  
Seasonal Changes ◽  
Size Range ◽  
Metabolic Rates ◽  
Seasonal Acclimatization ◽  
Temperature Range ◽  
Wild Rats

Wild rats were collected from dumps at Cornwall, Ontario, and Kingston, Ontario, during summer and winter, and oxygen consumption was measured at various temperatures from 30 °C to −61 °C. Oxygen consumption varied with body weight0.83 over a size range of 100 to 400 g and was slightly but significantly higher for males than for females. The relation of oxygen consumption to temperature was similar in rats collected during summer and winter over the temperature range from 20° to about −10 °C but at lower and higher temperatures winter rats had higher metabolic rates. When tested at −40° the oxygen consumption of winter-caught rats was maintained for at least 50 minutes while that of the summer-caught rats declined progressively. It is concluded that wild rats exhibit a metabolic acclimatization to seasonal changes in their environment.

scholarly journals Deep-sea echinoderm oxygen consumption rates and an interclass comparison of metabolic rates in Asteroidea, Crinoidea, Echinoidea, Holothuroidea and Ophiuroidea

2011 ◽  
Vol 214 (15) ◽  
pp. 2512-2521 ◽  
Author(s):  
S. J. M. Hughes ◽  
H. A. Ruhl ◽  
L. E. Hawkins ◽  
C. Hauton ◽  
B. Boorman ◽  
...  
Keyword(s):  
Oxygen Consumption ◽  
Deep Sea ◽  
Metabolic Rates ◽  
Consumption Rates

scholarly journals SUMMIT METABOLISM OF NEWBORN CALVES WITH AND WITHOUT COLOSTRUM FEEDING

1986 ◽  
Vol 66 (4) ◽  
pp. 937-944 ◽  
Author(s):  
M. OKAMOTO ◽  
J. B. ROBINSON ◽  
R. J. CHRISTOPHERSON ◽  
B. A. YOUNG
Keyword(s):  
Body Weight ◽  
Metabolic Rate ◽  
Rectal Temperature ◽  
Cold Water ◽  
Water Immersion ◽  
Resting Metabolic Rate ◽  
The Body ◽  
Metabolic Rates ◽  
Colostrum Feeding ◽  
Time Required

Resting and summit metabolic rates were measured in 13 newborn (2.5–15 h old) male Holstein calves exposed to warm and cold tempertures in a water immersion system. Six calves were bottle fed 1 kg of colostrum 30 min before the measurements commenced. In the remaining seven calves, colostrum was withheld until after the end of the measurement period. There were no significant effects of colostrum feeding on resting or summit metabolic rates or the time required for rectal temperature to drop to 35 °C when the calves were immersed in cold water. The time required for rectal temperature to drop to 35 °C increased as the body weight of the calves increased; for each kilogram additional body weight, cooling was delayed for an extra 2.9 min. The resting metabolic rate averaged for both feeding treatments was 2.0 ± 0.1 W kg−1 while mean rectal temperature was 39.1 ± 0.2 °C. Mean summit metabolic rate was 7.2 ± 0.4 W kg−1 and occurred at a mean rectal temperature of 35.4 ± 0.3 °C. The average ratio of the summit to resting metabolic rate was 3.7 ± 0.2. Cooling via water immersion was associated with increases in plasma levels of glucose and free fatty acids. The feeding of 1 kg of colostrum 30 min prior to exposure to acute cold did not improve the apparent resistance of the calves to hypothermia. Key words: Newborn calf, summit metabolism, cold tolerance

The Effects of Pituitrin and of Narcosis on Water-Regulation in Larval and Metamorphosed Amblystoma

1927 ◽  
Vol 5 (1) ◽  
pp. 89-96
Author(s):  
J. BĚLEHRÁDEK ◽  
J. S. HUXLEY
Keyword(s):  
Body Weight ◽  
Oxygen Consumption ◽  
Water Content ◽  
Water Intake ◽  
Larval Stage ◽  
The Body ◽  
Pituitary Extract ◽  
Water Regulation ◽  
Imperfect State ◽  
Water Equilibrium

(1) Injection of post-pituitary extract to larval and adult Amblystoma individuals leads to an increased water-intake, followed by a decrease in water-content the body, the decrease being greater than the preliminary increase. Repeated injections cause decreases of body-weight of over 35 per cent. (2) This effect runs parallel with the chromatophore effect. No change in oxygen consumption could be detected, even with long continued injection. (3) Both larval and metamorphosed Amblystoma lose weight (by loss of water) when narcotised in a solution of amytal 1 : 3000; the loss is greater in larval specimens; the decrease is followed, in metamorphosed animals, by a slight net increase. (4) Both the pituitary effect and the amytal effect develop considerably more quickly in larval than in metamorphosed Amblystoma. (5) The mechanism regulating the water-equilibrium of the body in Amblystoma passes, during metamorphosis, from a relatively imperfect state in the larval stage to a more efficient condition in adult individuals.

scholarly journals Body mass scaling of passive oxygen diffusion in endotherms and ectotherms

2016 ◽  
Vol 113 (19) ◽  
pp. 5340-5345 ◽  
Author(s):  
James F. Gillooly ◽  
Juan Pablo Gomez ◽  
Evgeny V. Mavrodiev ◽  
Yue Rong ◽  
Eric S. McLamore
Keyword(s):  
Oxygen Consumption ◽  
Body Mass ◽  
Oxygen Diffusion ◽  
The Body ◽  
Activity Levels ◽  
Mass Dependence ◽  
Diffusion Capacity ◽  
Aerobic Activity ◽  
Mass Scaling ◽  
Consumption Rates

The area and thickness of respiratory surfaces, and the constraints they impose on passive oxygen diffusion, have been linked to differences in oxygen consumption rates and/or aerobic activity levels in vertebrates. However, it remains unclear how respiratory surfaces and associated diffusion rates vary with body mass across vertebrates, particularly in relation to the body mass scaling of oxygen consumption rates. Here we address these issues by first quantifying the body mass dependence of respiratory surface area and respiratory barrier thickness for a diversity of endotherms (birds and mammals) and ectotherms (fishes, amphibians, and reptiles). Based on these findings, we then use Fick’s law to predict the body mass scaling of oxygen diffusion for each group. Finally, we compare the predicted body mass dependence of oxygen diffusion to that of oxygen consumption in endotherms and ectotherms. We find that the slopes and intercepts of the relationships describing the body mass dependence of passive oxygen diffusion in these two groups are statistically indistinguishable from those describing the body mass dependence of oxygen consumption. Thus, the area and thickness of respiratory surfaces combine to match oxygen diffusion capacity to oxygen consumption rates in both air- and water-breathing vertebrates. In particular, the substantially lower oxygen consumption rates of ectotherms of a given body mass relative to those of endotherms correspond to differences in oxygen diffusion capacity. These results provide insights into the long-standing effort to understand the structural attributes of organisms that underlie the body mass scaling of oxygen consumption.

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