Energy requirements for maintenance and faecal and urinary losses of the grey seal (Halichoerus grypus)

1984 ◽  
Vol 62 (6) ◽  
pp. 1101-1105 ◽  
Author(s):  
K. Ronald ◽  
K. M. Keiver ◽  
F. W. H. Beamish ◽  
R. Frank
Keyword(s):  
Energy Intake ◽  
Assimilation Efficiency ◽  
Metabolizable Energy ◽  
Energy Requirements ◽  
Halichoerus Grypus ◽  
Energy Losses ◽  
Atlantic Herring ◽  
Daily Food ◽  
Nitrogen Intake ◽  
Gross Energy

Assimilation efficiency of gross energy (±SD) in juvenile and adult grey seals fed Atlantic herring was 92.6 ± 2.1%. Metabolizable energy (ME) was 82.7 ± 4.8% of gross energy intake. Faecal energy losses increased directly with energy intake and urinary energy losses increased directly with apparent digestible nitrogen intake. Maintenance energy requirements were estimated at 4215 kcal (1 cal = 4.1868 J) ME daily for both juvenile and adult seals, equivalent to daily food intakes of 3.0–3.2 and 1.5% of body weight for juvenile and adults, respectively.

Metabolizable energy requirements for maintenance and faecal and urinary losses of juvenile harp seals (Phoca groenlandica)

1984 ◽  
Vol 62 (5) ◽  
pp. 769-776 ◽  
Author(s):  
K. M. Keiver ◽  
K. Ronald ◽  
F. W. H. Beamish
Keyword(s):  
Energy Intake ◽  
Weight Change ◽  
Assimilation Efficiency ◽  
Metabolizable Energy ◽  
Energy Requirements ◽  
Energy Losses ◽  
Feeding Frequency ◽  
Phoca Groenlandica ◽  
High Lipid ◽  
Gross Energy

Assimilation efficiency of energy in juvenile harp seals was 92.5–95.0% of gross energy intake when fed Atlantic herring and 72.2% when fed shrimp. Faecal energy losses increased directly with intake. Metabolizable energy (ME) ranged from 85.5 to 88.7% of gross energy intake for a diet of herring. Urinary energy losses increased directly with apparent digestible nitrogen intake. Faecal and urinary losses were not affected significantly by feeding frequency. Urine excretion indicated that feeding causes a diuresis, associated with increased energy, nitrogen, and ash excretion. A significant interaction was found for rate of weight change between feeding frequency and energy intake. Seals lost more weight at energy intakes below their maintenance level when fed four meals rather than two meals per day. Differences in rate of weight change with feeding frequency were not observed at other levels of energy intake. Maintenance energy requirements were estimated at 2658 kcal ME daily for seals fed two meals per day and 3514 kcal ME daily when fed four meals per day. Seals required approximately 3 times as much shrimp as herring of high lipid content to meet their energy requirements.

Metabolizable energy of fish when fed to captive Great Blue Herons (Ardea herodias)

1993 ◽  
Vol 71 (9) ◽  
pp. 1767-1771 ◽  
Author(s):  
Darin C. Bennett ◽  
Leslie E. Hart
Keyword(s):  
Energy Intake ◽  
Energy Content ◽  
Nitrogen Retention ◽  
Metabolizable Energy ◽  
Clupea Harengus ◽  
Energy Losses ◽  
Ardea Herodias ◽  
Apparent Metabolizable Energy ◽  
Gross Energy ◽  
Energy Coefficient

The efficiency with which the gross energy content of herring (Clupea harengus), mackerel (Scomber scombrus), and trout (Oncorhynchus mykiss) is metabolized was determined for 11 captive Great Blue Herons (Ardea herodias). There was a linear relationship between apparent metabolized energy and gross energy intake for the mackerel and trout. This relationship was lower and more variable for herring. Estimates of the apparent metabolizable energy coefficient for mackerel and trout were affected by the level of energy intake. Correcting for endogenous energy losses in the excreta yielded estimates of true metabolizable energy coefficients that were independent of gross energy intake. The true metabolizable energy coefficient of mackerel and trout did not differ and averaged 0.866 (SD = 0.014, n = 3 diets). Correcting for nitrogen retention did not improve the estimate of the metabolizable energy coefficient. The metabolizable energy coefficient of herring was highly variable and showed no consistent pattern in relation to energy intake.

The energy value to ruminants of malt distillers' draff, and of a mixture of draff and pot ale syrup

1982 ◽  
Vol 34 (3) ◽  
pp. 325-328 ◽  
Author(s):  
F. W. Wainman ◽  
P. J. S. Dewey
Keyword(s):  
Energy Intake ◽  
Crude Protein ◽  
Dry Matter ◽  
Metabolizable Energy ◽  
Energy Losses ◽  
Short Term ◽  
Gross Energy ◽  
Second Period ◽  
By Products ◽  
Copper Poisoning

ABSTRACTTwo foods, distillers' wet draff and draff plus pot ale syrup, containing 207 and 256 g crude protein per kg dry matter respectively, were given as sole food at the maintenance level to four adult wether sheep. Two of the sheep were given draff and two draff plus syrup for a 28-day period; the treatments were then changed over for a second period. The copper contents of the foods were 17 and 30mg/kg dry matter for the draff and draff plus syrup respectively. Sheep are particularly susceptible to copper and care should be taken when feeding such by-products, but during these short-term trials there was no evidence of copper poisoning. Energy losses in the faeces and urine were measured for all sheep, and methane losses were measured in closed-circuit respiration chambers for two sheep on each treatment. The metabolizable energy values of the foods were 10·8 (s.e. 0·15) and 12·5 (s.e. 0·15) MJ/kg dry matter for the draff and draff plus syrup respectively. The proportions of gross energy intake lost as methane were 0·029 for the draff and 0·042 for the draff plus syrup; these were much lower than the values predicted by the commonly used equation.

Effect of air temperature and energy intake on body mass, body composition and energy requirements in sheep

2002 ◽  
Vol 138 (2) ◽  
pp. 221-226 ◽  
Author(s):  
A. ALLAN DEGEN ◽  
B. A. YOUNG
Keyword(s):  
Energy Intake ◽  
Body Mass ◽  
Air Temperature ◽  
Total Body Water ◽  
Metabolizable Energy ◽  
Energy Requirements ◽  
Water Volume ◽  
Air Temperatures ◽  
Metabolizable Energy Intake ◽  
Total Body

Body mass was measured and body composition and energy requirements were estimated in sheep at four air temperatures (0 °C to 30 °C) and at four levels of energy offered (4715 to 11785 kJ/day) at a time when the sheep reached a constant body mass. Final body mass was affected mainly by metabolizable energy intake and, to a lesser extent, by air temperature, whereas maintenance requirements were affected mainly by air temperature. Mean energy requirements were similar and lowest at 20 °C and 30 °C (407·5 and 410·5 kJ/kg0·75, respectively) and increased with a decrease in air temperature (528·8 kJ/kg0·75 at 10 °C and 713·3 kJ/kg0·75 at 0 °C). Absolute total body water volume was related positively to metabolizable energy intake and to air temperature. Absolute fat, protein and ash contents were all affected positively by metabolizable energy intake and tended to be related positively to air temperature. In proportion to body mass, total body water volume decreased with an increase in metabolizable energy intake and with an increase in air temperature. Proportionate fat content increased with an increase in metabolizable energy intake and tended to increase with an increase in air temperature. In contrast, proportionate protein content decreased with an increase in metabolizable energy intake and tended to decrease with an increase in air temperature. In all cases, the multiple linear regression using both air temperature and metabolizable energy intake improved the fit over the simple linear regressions of either air temperature or metabolizable energy intake and lowered the standard error of the estimate. The fit was further improved and the standard error of the estimate was further lowered using a polynomial model with both independent variables to fit the data, since there was little change in the measurements between 20 °C and 30 °C, as both air temperatures were most likely within the thermal neutral zone of the sheep. It was concluded that total body energy content, total body water volume, fat and protein content of sheep of the same body mass differed or tended to differ when kept at different air temperatures.

scholarly journals Growth and Energy Requirements of Captive-Reared Common Loon (Gavia Immer) Chicks

The Auk ◽  
2007 ◽  
Vol 124 (4) ◽  
pp. 1158-1167
Author(s):  
François Fournier ◽  
William H. Karasov ◽  
Kevin P. Kenow ◽  
Michael W. Meyer
Keyword(s):  
Growth Rate ◽  
Body Mass ◽  
Developmental Change ◽  
Assimilation Efficiency ◽  
Bird Species ◽  
Metabolizable Energy ◽  
Energy Requirements ◽  
Growth Rate Constant ◽  
Gavia Immer ◽  
Common Loon

AbstractWe measured the energy requirements during postnatal development of six hand-reared Common Loon (Gavia immer) chicks using continuous feeding trials and doubly labeled water. At fledging, the mean (± SE) body mass of chicks was 3,246 ± 51 g. They reached asymptotic body mass in ≈66 days and had a mean growth rate constant of 0.089 ± 0.002 day−1, which was greater than growth rate constants of other, similar-sized precocial birds. Between hatch and day 66, chicks allocated 16.5% of their metabolizable energy to new tissue, lower than the average for other bird species (20%), which might be expected considering their precocial mode of development. There was a developmental change in the assimilation efficiency of food (metabolizable energy coefficient), with a mean of 0.64 ± 0.03 in chicks aged 21 days, rising to 0.83 ± 0.07 in chicks aged 35 days.Les besoins en énergie durant la croissance chez des jeunes Gavia immer élevés en captivité

The effect of genetic merit and concentrate proportion in the diet on nutrient utilization by lactating dairy cows

1999 ◽  
Vol 132 (4) ◽  
pp. 483-490 ◽  
Author(s):  
C. P. FERRIS ◽  
F. J. GORDON ◽  
D. C. PATTERSON ◽  
M. G. PORTER ◽  
T. YAN
Keyword(s):  
Dairy Cows ◽  
Energy Intake ◽  
Milk Production ◽  
Milk Fat ◽  
Nutrient Utilization ◽  
Metabolizable Energy ◽  
Energy Utilization ◽  
Energy Output ◽  
Genetic Merit ◽  
Gross Energy

Sixty Holstein/Friesian dairy cows, 28 of high genetic merit and 32 of medium genetic merit, were used in a continuous design, 2 (cow genotypes)×4 (concentrate proportion in diet) factorial experiment. High and medium merit animals had Predicted Transmitting Abilities for milk fat plus protein yield, calculated using 1995 as the base year (PTA95 fat plus protein), of 43·3 kg and 1·0 kg respectively. Concentrate proportions in the diet were 0·37, 0·48, 0·59 and 0·70 of total dry matter (DM), with the remainder of the diet being grass silage. During this milk production trial, 24 of these animals, 12 from each genetic merit, representing three animals from each concentrate treatment, were subject to ration digestibility, and nitrogen and energy utilization studies. In addition, the efficiency of energy utilization during the milk production trial was calculated.There were no genotype×concentrate level interactions for any of the variables measured (P>0·05). Neither genetic merit nor concentrate proportion in the diet influenced the digestibility of either the DM or energy components of the ration (P>0·05). When expressed as a proportion of nitrogen intake, medium merit cows exhibited a higher urinary nitrogen output and a lower milk nitrogen output than the high merit cows. Methane energy output, when expressed as a proportion of gross energy intake, was higher for the medium than high merit cows (P<0·05), while urinary energy output tended to decrease with increasing proportion of concentrate in the diet (P<0·05). In the calorimetric studies, neither heat energy production, milk energy output and energy retained, when expressed as a proportion of metabolizable energy intake, nor the efficiency of lactation (kl), were affected by either cow genotype or concentrate proportion in the diet (P>0·05). However when kl was calculated using the production data from the milk production trial the high merit cows were found to have significantly higher kl values than the medium merit cows (0·64 v. 0·59, P<0·05) while k l tended to fall with increasing proportion of concentrate in the ration (P<0·05). However in view of the many assumptions which were used in these latter calculations, a cautious interpretation is required.

Energy intake and patterns of growth for male and female fallow deer of two genotypes, between 10 and 21 months of age

2000 ◽  
Vol 70 (2) ◽  
pp. 335-342
Author(s):  
R.C. Mulley ◽  
G.W. Asher ◽  
J.S. Flesh ◽  
K.T. O’Neill ◽  
J. Ferguson
Keyword(s):  
Body Weight ◽  
Weight Gain ◽  
Energy Intake ◽  
Live Weight ◽  
Fallow Deer ◽  
Metabolizable Energy ◽  
Dama Dama ◽  
Significant Difference ◽  
Gross Energy ◽  
Feeding Systems

AbstractEuropean (no. = 36) and hybrid (¼ Mesopotamian, ¾ European; no. = 36) fallow deer (Dama dama) were evaluated for weight gain and energy intake from 10 to 21 months of age. Twelve each of bucks, does and castrated males (haviers) were tested for each genotype, in both concentrate-fed and pasture-based feeding systems. Based on weekly weighing hybrids (H) in each of the sex classes grew more rapidly (5 g/day across all groups) than the European (E) fallow deer (P < 0·05). Haviers given concentrates grew significantly faster than pasture-fed haviers (P < 0·01), whilst does grown on pasture grew significantly faster than those given concentrates (P < 0·01). There was no significant difference in pattern of growth between bucks on pasture and those given concentrates (P > 0·05). Does grew significantly less (P < 0·01) than bucks and haviers in spring, summer and winter but environmental differences between years could not be accounted for in the analysis.Animals of all sexes and genotypes experienced rapid growth from 10 to 12 months of age (spring) and this was associated with energy intakes according to metabolic body weight (M0·75) these ranging between 0·8 and 1·1 MJ metabolizable energy (ME) per kg M0·75 per day. There were significantly (P < 0·01) higher levels of energy consumed by H does and haviers in the summer, compared with their E counterparts but this was not associated with greater growth rates. However, H does had significantly higher (P < 0·01) dressing proportions at slaughter than E does. The energy intake on a metabolic body weight basis for most groups declined to between 0·7 and 0·8 MJ ME per kg M0·75 per day from 12 to 21 months of age, except for the does, which declined even further to between 0·5 and 0·6 MJ ME per kg M0·75 per day from 17 months of age.There were no significant differences between E and H deer for energy intakes per M0·75, and H deer were slightly more energy efficient than their E counterparts in terms of growth rate in relation to annual gross energy intake. The food intake : weight gain ratio increased considerably for both genotypes after 14 months of age, indicating the desirability for slaughtering as soon as animals reach the target live weight. It was concluded that the crossbreeding system described is production efficient and produced offspring that reached slaughter weight sooner than E fallow deer and thereby produced carcasses with a greater wholesale value than their E counterparts of the same age.

Observations on the Food and Energy Requirements of Rainbow Lorikeets, Trichoglossus Haematodus (Aves:Psittacidae).

1979 ◽  
Vol 6 (3) ◽  
pp. 337 ◽  
Author(s):  
CE Cannon
Keyword(s):  
Energy Intake ◽  
Energy Cost ◽  
Milk Powder ◽  
Energy Requirements ◽  
Restricted Diet ◽  
Fortified Milk ◽  
Sufficient Energy ◽  
Gross Energy ◽  
Maintenance Requirements

Captive Trichoglossus haematodus were given a restricted diet of bread and honey or a supplemented diet of bread, honey and the fortified milk powder 'Complan'. On the former diet they lost weight and were less active compared to those on the latter. Both diets were very fluid and birds consumed the equivalent of 38 to 47% of their bodyweight daily. However, they ate significantly more of the supplemented diet, 15.1 g DM daily, than of the bread and honey diet, 12.8 g daily. Birds given the supplemented diet voided more excreta and lost more excretory energy, 28.9 kJ/day, than the others, 17.9 kJ/day, but the 2 groups did not differ in their gross energy intake or maintenance requirements. A captive lorikeet weighing about 150 g required about 230 kJ/day for existence, with an efficiency of food use of 89%. Allowing a higher energy cost for free existence, it is suggested that wild lorikeets could gather sufficient energy daily in 2.5 h.

Meta-analysis on the effects of lipid supplementation on methane production in lactating dairy cows

2008 ◽  
Vol 88 (2) ◽  
pp. 331-337 ◽  
Author(s):  
M. Eugène ◽  
D. Massé ◽  
J. Chiquette ◽  
C. Benchaar
Keyword(s):  
Dairy Cows ◽  
Energy Intake ◽  
Milk Production ◽  
Meta Analysis ◽  
Milk Composition ◽  
Metabolizable Energy ◽  
Scientific Publications ◽  
Lactating Dairy Cows ◽  
Gross Energy ◽  
Lipid Supplementation

A meta-analysis was conducted to statistically determine the effects of lipid supplementation on methane (CH4) production, milk production, and milk composition of lactating dairy cows. For this purpose, a data base was built using seven scientific publications (25 diets) available in the literature and reporting the effects of lipid supplementation on CH4 production, milk production, and milk composition. Lipid supplementation decreased (P < 0.05) dry matter intake (DMI) by 6.4% compared with control diets, whereas production of milk and 4% FCM and milk composition were not changed (P > 0.05). Lipid supplementation decreased (P < 0.05) CH4 production by 9%, either expressed as MJ d-1 or as a percentage of gross energy intake (GEI), digestible energy intake (DEI), or metabolizable energy intake (MEI). This reduction was mainly a consequence of a decreased DMI. Key words: Meta-analysis, lipid supplementation, methane, dairy cows, lactating

Nutritional evaluation of winter foods of wild turkeys

1991 ◽  
Vol 69 (8) ◽  
pp. 2128-2132 ◽  
Author(s):  
Scott R. Decker ◽  
Peter J. Pekins ◽  
William W. Mautz
Keyword(s):  
Energy Intake ◽  
Energy Content ◽  
Meleagris Gallopavo ◽  
Metabolizable Energy ◽  
Red Oak ◽  
Rosa Multiflora ◽  
Gross Energy ◽  
Multiflora Rose ◽  
Wild Turkeys ◽  
Metabolizable Energy Intake

Red oak acorns (Quercus rubra), fruits of multiflora rose (Rosa multiflora), common juniper (Juniper communis), winterberry holly (Ilex verticillata), and barberry (Berberis spp.), fertile fronds of sensitive fern (Onoclea sensibilis), corn, and apples were fed as mixed rations to eight eastern wild turkeys (Meleagris gallopavo silvestris). Crude protein content of the foods ranged from 2 (apples) to 19% (sensitive fern). Red oak acorns and juniper berries were 14% fat; other foods were 1–7% fat. Apples were lowest in gross energy content (3.9 kcal/g dry matter (1 cal = 4.1868 J)), and sensitive fern was highest (5.5 kcal/g). Little variation existed in nutrient composition and energy content of the mixed diets. Metabolizable energy values of the diets ranged from 65 to 84% of gross energy intake and from 3.1 to 4.0 kcal/g. Solution of simultaneous equations based on the mixed-diet data yielded metabolizable energy values of individual foods; juniper had the highest metabolizable energy (4.6 kcal/g) and sensitive fern the lowest (2.1 kcal/g); other foods ranged from 3.3 to 4.1 kcal/g. Acorns, corn, and shrubs with persistent fruits (juniper, winterberry, barberry, and multiflora rose) were the most nutritious foods. Metabolizable energy intake of the mixed diets, excluding the juniper-dominated diet, approximated or exceeded the predicted daily energy expenditure of wild turkeys.

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