Economic losses from heat stress by us livestock industries

Factors influencing the structure and function of the small intestine in the weaned pig: a review

Effects of climate changes on animal production and sustainability of livestock systems

A review of interactions between dietary fibre and the intestinal mucosa, and their consequences on digestive health in young non-ruminant animals

Feeding behaviour feedback signals ruminant gastrointestinal tract metabolites and hormones central nervous control integrative theories of food intake control growth and fattening reproduction and lactation diet digestability and concentration of available energy specific nutrients affecting intake learning about food - preferences diet selection appetites for specific nutrients environmental factors affecting intake the intake of fresh and conserved grass prediction of voluntary intake. Appendices: particular features of poultry and ruminant animals outline programme to identify and store meals from the identities of animals and weights of food containers.

Voluntary food intake and diet selection in farm animals.

Digestible (DE), metabolizable (ME), and net (NE) energy values of 61 diets were measured in 45-kg growing Large White boars. Net energy was calculated as energy retained at an average ME intake equivalent to 540 kcal/kg BW.60 plus fasting heat production estimated from data of the present experiment as 179 kcal/kg BW.60. Retained energy was measured as the difference between ME intake and heat production obtained in respiration chambers. The amounts of DE digested before the end of the ileum (DEi) and in the hindgut (DEh) were also measured for each diet. Regression equations for predicting dietary NE content from digestible nutrient levels or from DE or ME and chemical characteristics or from chemical composition only were calculated. Efficiencies of utilization of ME for NE (k, %) were also obtained. The mean k value for the 61 diets was 74% (range: 69 to 77). Digestible nutrients were used differently for NE: k values varied from approximately 60% for digestible CP or digestible cell wall fractions to 82% for starch and 90% for digestible ether extract. Accordingly, k for ME associated with DEh was lower than ME from DEi (58 vs 76%). Equations for predicting NE content are proposed. Their applicability, the comparison with other available NE prediction equations, and the effects of energy system on diet formulation are discussed.

Prediction of net energy value of feeds for growing pigs

The DE and ME values and digestible nutrient contents of 114 diets were measured in 45-kg growing pigs (four to five animals per diet) fed approximately 500 kcal of ME/kg BW60 Diets differed widely with regard to their chemical characteristics and their ingredients Chemical composition of each diet was measured by at least four laboratories The results were used to establish prediction equations of DE or ME values, digestible nutrient contents, and digestibility coefficients of energy and nutrients from chemical characteristics Digestibility coefficients of energy (range: 65 to 95%) and CP (range: 64 to 94%) were highly dependent on dietary fiber and mineral contents The digestibility coefficient of ether extract increased curvilinearly (from 2 to 84%) with the dietary fat content The digestibility of fiber was lower (45%, for NDF) than for the other chemical consti- tuents The ME:DE ratio averaged 963% and was negatively correlated to the dietary protein content The DE and ME values could be accurately predicted (R2 > 90 and CV < 2%) from chemical characteristics; the best equations were obtained when the following predictors were combined in a linear model: ash, ether extract, crude protein, and an estimate of dietary fiber The accuracy of the prediction was higher with NDF than with ADF or Weende crude fiber The results suggest that even a rather large proportion of dietary fiber (approximately 50%) is degraded in the digestive tract, the amount of available energy from fiber digestion is negligible in connection with in- creased endogenous protein and fat losses The equa- tions obtained in the present, study represent a basis for the prediction of the energy values of mixed diets with a composition of unknown ingredients

Prediction of digestibility of nutrients and energy values of pig diets from chemical analysis.

Effect of dietary fibre on the energy value of feeds for pigs

Multiparous Large White sows (n = 63) were used to investigate the effects of five ambient temperatures (18, 22, 25, 27, and 29 degrees C) and two dietary protein contents on their lactation performance. At each temperature treatment, ambient temperature was maintained constant over the 21-d lactation period. Dietary protein content was either 14 or 17% with essential amino acids levels calculated not to be limiting. The animals had ad libitum access to feed between the seventh and the 19th day of lactation. Diet composition did not influence lactation performance. Over the 21-d lactation, feed intake decreased from 5.67 to 3.08 kg/d between 18 and 29 degrees C. Between d 7 and 19, the corresponding values were 7.16 and 3.48 kg/d, respectively. This decrease was curvilinear; an equation to predict voluntary feed intake (VFI) from temperature (T, degrees C) and body weight (BW, kg) is proposed: VFI = -49,052 + 1,213 T - 31.5 T2 + 330 BW - .61 BW2 (residual standard deviation: 1,018). Skin temperature increased regularly with increased ambient temperature (34.6 to 37.4 degrees C between 18 and 29 degrees C), whereas udder temperature reached a plateau at 25 degrees C (38.3 degrees C). The gradient of temperature between skin and rectum was minimal (2 degrees C ) at 27 degrees C and remained constant at 29 degrees C. This constancy coincides with the marked reduction of feed intake. The respiratory rate increased from 26 to 124 breaths/min between 18 and 29 degrees C, and this indicates that the evaporative critical temperature was below 22 degrees C. The BW loss increased from 23 to 35 kg between 18 and 29 degrees C, but its estimated chemical composition remained constant. Pig growth rate was almost constant between 18 and 25 degrees C (241 g/d) and was reduced above 25 degrees C (212 and 189 g/d at 27 and 29 degrees C, respectively). In conclusion, temperatures above 25 degrees C seem to be critical for lactating sows in order to maintain their performance.

Influence of high ambient temperatures on performance of multiparous lactating sows

An experiment was conducted in which the metabolic utilization of energy was measured in individually penned pigs from seven groups that differed in genotype and(or) sex and ranged in body weight between 20 and 107 kg. The animals were fed a diet containing, on a DM basis, 14.7 MJ ME and at least 21% CP. Heat production was measured in an open-circuit calorimeter, and energy, nitrogen, and fat balances were determined at regular intervals over the growing period; a total of 177 measurements were performed. Body composition of the animals was measured by serial slaughter, and these data were used for estimating the body composition of an animal at a given weight through allometric regression. A factorial analysis procedure was used to estimate the utilization of ME by regressing the ME intake on the observed protein and lipid deposition rates. The intercept of this equation is the maintenance energy requirement (MEm) and was represented either as a function of body weight with group-specific parameters (MEm = a(i) BWb) or as a function of the muscle and visceral mass with an additional additive group effect (MEm = aM muscle(b) + a(v) viscera(b) + G(i)). With BW as dependent variable, the exponent b was close to .60 and differed significantly from .75. The regression coefficient (a(i)) averaged 1.02 MJ ME/kg.60 but it was different for most groups, indicating that different groups of animals have different maintenance requirements. Fixing the exponent to .75 consistently underestimated the maintenance requirement. When the exponent b was not fixed to .75 but estimated, the partial efficiencies for protein and lipid deposition were .62 and .84, respectively. Body muscle and visceral mass could explain a large part of the variation in MEm. Viscera contributed three times more to MEm (per kilogram of mass raised to the .70 power) than did muscle. Even though the muscle mass exceeds to a large extent the visceral mass in animals, the contribution of muscle to MEm was lower than that of viscera for most groups.

Jean Noblet

Papers

Prediction of net energy value of feeds for growing pigs

Prediction of digestibility of nutrients and energy values of pig diets from chemical analysis.

Effect of dietary fibre on the energy value of feeds for pigs

Influence of high ambient temperatures on performance of multiparous lactating sows

Metabolic utilization of energy and maintenance requirements in growing pigs: effects of sex and genotype.