On farm precision feeding of gestating sows based on energy and amino acids on farrowing performances and feeding behavior over three consecutive gestations.

Gestating sows are often fed a single diet throughout their gestation cycle, leading to situations of nutrients deficiency or excess at the individual level. The purpose of this study was to characterize, over 3 consecutive cycles, the impact of a precision feeding (PF), i.e. dietary supplies adjusted at individual level in terms of quantity (energy intake) and quality (standardized ileal digestible (SID) lysine (Lys) intake), on gestating sows' productive performance, feeding behavior, environmental outputs and health status compared with sows fed a conventional feeding (CF, i.e. fixed SID Lys intake). At the start of the trial, 2 batches of 20 Landrace × Large White gestating sows were allocated to one of the 2 feeding strategies (PF vs. CF), based on their parity (1, 2 or 3 and more), body weight (BW), and backfat thickness (BT) 3 days after insemination. The PF strategy consisted in mixing with automatic feeders 2 iso-energetic diets (9.8 MJ/kg of net energy with 3.3 and 8.5 g SID Lys / kg, respectively) in variable proportions at individual and daily levels, whereas for the CF strategy these proportions remained constant throughout gestation (73% and 27%, respectively, resulting in a SID Lys concentration of 4.7 g/kg). Sows were followed over 3 consecutive gestations and the sows remained allocated to the same strategy throughout the study. Some sows were culled before the end of the study and were replaced by other sows who therefore performed only 1 or 2 gestations during the study. Thus, 106 gestations and lactations from 51 sows were fully studied and their data analyzed. The PF strategy allowed the sows to reach more closely the expected BT values at farrowing across cycles than the CF strategy (P < 0.001). The PF sows consumed 16% less SID Lys per gestation than the CF sows (P < 0.001), resulting in a 4% improvement in N efficiency (P < 0.001), with no impact on performance at farrowing (P > 0.10). The sows consumed their daily ration in a single visit whatever the feeding strategy (P = 0.41), but CF sows spent more time in the feeder in cycle 2 and 3 (P < 0.001). Thus, compared to the CF strategy implemented by farmers, the individual and daily nutritional supplies implemented with the PF strategy were more efficient in enabling sows to achieve body condition objectives at farrowing over the long-term, also with a reduced SID Lys intake and an improved N efficiency without negative impact on farrowing performances.

Supplying dextrose before insemination and L-arginine during the last third of pregnancy in sow diets: effects on within-litter variation of piglet birth weight.

Preweaning piglet mortality is largely attributed to the incidence of low birth weight and birth weight variation within the litter. Therefore, developing strategies to increase within-litter uniformity of piglet birth weight is important. This study investigated the effects of different feeding strategies based on specific nutrient supplies in sow diet on the within-litter variation of piglet birth weight (BW0). Four batches of highly prolific crossbred Landrace × Large White sows were used. Three dietary treatments were compared: supplies of dextrose during the week before insemination (190 g/d) and of L-arginine (25.5 g/d) from d 77 of pregnancy until term (DEXA, n = 26); a dietary supplementation of L-arginine only (25.5 g/d), from d 77 of pregnancy until term (ARGI, n = 24); and no supplementation to a standard gestation diet (CTL; n = 23). Total born piglets (TB), i.e., piglets born alive (BA) and stillborn piglets, were numbered and weighed at birth and at weaning. Data were analyzed by ANOVA using the MIXED procedure in a model that included dietary treatment (ARGI, DEXA, and CTL), initial parity (1, 2 and 3, 4, and more), and backfat thickness (below or above the average value at the onset of the experiment: 15.7 mm) as the main effects and batch as random effect. The treatment did not influence (P > 0.10) the number of piglets at birth (on average 15.6 ± 3.8 and 14.2 ± 3.6 for TB and BA, respectively) or piglet BW0 (on average 1.48 ± 0.26 and 1.50 ± 0.26 kg for TB and BA, respectively). The coefficient of variation of piglet BW0 (CV(BW0)) was less in litters from ARGI sows than in litters from CTL sows and intermediate in litters from DEXA sows (for TB: 21.4, 23.4, and 25.7%, P = 0.08; for BA: 20.6, 22.5, and 25.4%, P = 0.03, in the ARGI, DEXA, and CTL groups, respectively). Irrespective of diet, CV(BW0) was less (P < 0.01) in litters with 16 TB piglets or less than in the largest litters (20.9 vs. 26.5%). Litter growth rate during lactation and litter size at weaning were not influenced (P > 0.10) by dietary treatments. In conclusion, supplementing gestation diet with L-arginine during the last third of pregnancy reduced within-litter variation of piglet birth weight. Combining L-arginine dietary supply with a supplementation of dextrose before insemination provided no additional benefit.

The effect of immunization against GnRF on nutrient requirements of male pigs: a review.

In most countries, male pigs are physically castrated soon after birth to reduce the risk of boar taint and to avoid behaviours such as fighting and mounting. However, entire male pigs are more feed efficient and deposit less fat than barrows. In addition, many animal welfare organizations are lobbying for a cessation of castration, with a likelihood that this could lead to inferior pork unless an alternative method is used to control boar taint. An alternative to physical castration is immunization against gonadotrophin releasing factor (GnRF) which allows producers to capitalize on the superior feed efficiency and carcass characteristics of boars without the risk of boar taint. From a physiological perspective, immunized pigs are entire males until shortly after the second dose, typically given 4 to 6 weeks before slaughter. Following full immunization, there is a temporary suppression of testicular function and a hormonal status that resembles that of a barrow. Nutrient requirements will be different in these two phases, before and after full immunization. Given that there have been few published studies comparing the lysine requirements of entire males and barrows in contemporary genotypes, it is useful to use gilt requirements as a benchmark. A series of meta-analyses comparing anti-GnRF immunized boars and physical castrates and use of nutritional models suggest that the lysine requirement of entire males before the second immunization is 5% higher than for gilts, from 25 to 50 kg BW, and by 8% from 50 to 95 kg. Given that the penalty in growth performance for having inadequate dietary lysine is greater in males than in gilts or barrows, it is important to ensure that lysine requirements are met to obtain the maximum benefits of entire male production during this phase. After the second immunization, the lysine requirement of immunized males decreases and may become more like that of barrows. In addition, a consistent effect of full immunization is a marked increase in voluntary feed intake from about 10 days after the second dose. Putting these together, the estimated lysine requirement, expressed in terms of diet composition, falls to 94% of the gilt level. Although general principles can be described now, further research is needed to fully define the lysine requirements of immunized boars. It is important that the temporal pattern of tissue deposition rates and feed intake be explored to be incorporated into models to predict nutrient requirements over the period of rapidly changing metabolism.

Accounting for variability among individual pigs in deterministic growth models.

Inclusion of variation in deterministic nutritional models for growth by repeating simulations using different sets of parameters has been performed in literature without or with only hypothetic consideration of the covariance structure among parameters. However, a description of the structure of links among parameters describing individuals is required to generate realistic sets of parameters. In this study, the mean and covariance structure of model parameters describing feed intake and growth were analyzed from 10 batches of crossbred gilts and barrows. Data were obtained from different crossbreeds, originating from Large White × Landrace sows and nine sire lines. Pigs were group-housed (12 pigs/pen) and performance testing was carried out from 70 days of age to ∼110 kg BW. Daily feed intake (DFI) was recorded using automatic feeding stations and BW was measured at least every 3 weeks. A growth model was used to characterize individual pigs based on the observed DFI and BW. In this model, a Gompertz function was used to describe protein deposition and the resulting BW gain. A gamma function (expressing DFI as multiples of maintenance) was used to express the relationship between DFI and BW. Each pig was characterized through a set of five parameters: BW70 (BW at 70 days of age), B(Gompertz) (a precocity parameter) PDm (mean protein deposition rate) and DFI50 and DFI100 (DFI at 50 and 100 kg BW, respectively). The data set included profiles for 1288 pigs for which no eating or growth disorders were observed (e.g. because of disease). All parameters were affected by sex (except for BW70) and batch, but not by the crossbreed (except for PDm). An interaction between sex and crossbreed was observed for PDm (P < 0.01) and DFI100 (P = 0.05). Different covariance matrices were computed according to the batch, sex, crossbreed, or their combinations, and the similarity of matrices was evaluated using the Flury hierarchy. As covariance matrices were all different, the unit of covariance (subpopulation) corresponded to the combination of batch, sex and crossbreed. Two generic covariance matrices were compared afterwards, with (median matrix) or without (raw matrix) taking into account the size of subpopulations. The most accurate estimation of observed covariance was obtained with the median covariance matrix. The median covariance matrix can be used, in combination with average parameters obtained on-farm, to generate virtual populations of pigs that account for a realistic description of mean performances and their variability.

Effect of feed restriction on the performance and behaviour of pigs immunologically castrated with Improvac®.

For centuries, entire male pigs have been castrated to reduce the risk of boar taint. However, physical castration of pig is increasingly being questioned with regard to animal welfare considerations. Immunization against gonadotrophin releasing hormone (GnRH) provides an alternative to physical castration. Using the currently available commercial product (Improvac®; Pfizer Animal Health), a two-dose regimen of a GnRH vaccine is administered. After the second vaccination, a substantial increase in feed consumption has been reported, which may be associated with increased body fatness and decreased feed efficiency when compared with unvaccinated entire male pigs. The aim of the present study was to investigate the effect of a feed restriction on these traits and on the behaviour of 120 group-housed entire males (five pigs/pen) vaccinated against GnRH. The first vaccination was performed at 62 days of age and the second (V2) at 130 days of age. Pigs were slaughtered in two batches 4 to 5 weeks after V2. They were either offered feed ad libitum over the 22 to 114 kg BW range (AL treatment) or ad libitum up to a maximum of 2.50 (R2.50 treatment) or 2.75 kg/day per pig (R2.75 treatment). Behavioural observations and skin lesion scoring were conducted 1 week before V2, and 1 and 3 weeks after V2. At slaughter, the volumetric lean meat content was measured using an X-ray computed tomography scanner. Between V2 and slaughter, the average feed intakes for the R2.75 and R2.50 treatments were 15% and 22% lower than the average AL feed intake (3.20 kg/day), respectively. Feed restriction was associated with a reduced average daily gain after V2 (846, 932 and 1061 g/day in the R2.50, R2.75 and AL groups, P < 0.01) but had no effect on the feed conversion ratio (3.00 kg feed/kg BW gain on average, P = 0.62). No difference was observed in the lean meat content (71.8%, 70.7% and 70.4% in the R2.50, R2.75 and AL groups, P = 0.14), despite a reduced backfat thickness measured in restrictively fed pigs (12.0, 13.0 and 13.6 mm in the R2.50, R2.75 and AL groups, P < 0.01). Higher skin lesion scores were observed 3 weeks after V2 in R2.50 and R2.75 pigs than in the AL ones (scores 33.4, 27.7 and 25.5, respectively, P = 0.04). These results, combined with an unimproved feed efficiency and no marked change in carcass characteristics, suggest that immunologically castrated pigs should not be restrictively fed during the late finishing period.

Effect of the dietary net energy concentration on feed intake and performance of growing-finishing pigs housed individually.

The effect of dietary NE content on feed intake and performance of pigs was investigated using crossbred barrows with initial and final BW of approximately 35 and 110 kg, respectively. Pigs were housed individually and allowed ad libitum access to feed. Pigs were randomly allotted to 6 wheat and soybean meal-based diets (8.1, 8.7, 9.3, 9.9, 10.5, and 11.1 MJ NE/kg) with 16 pigs/diet. Ratios between standardized ileal digestible AA and NE were similar in all diets. Over the entire experiment, increase in dietary NE concentration was associated with a decreased ADFI (3.216, 3.216, 3.122, 2.910, 2.732, and 2.684 kg/d, respectively, for diets containing 8.1 to 11.1 MJ NE/kg; linear, P < 0.01). The NE intake increased as dietary NE increased from 8.1 to 11.1 MJ NE/kg (26.04, 27.98, 29.03, 28.81, 28.68, and 29.77 MJ/d, respectively; linear, P < 0.01, and quadratic, P = 0.06). Average daily gain increased when dietary NE concentration increased (1.046, 1.126, 1.135, 1.177, 1.156, and 1.152 kg/d, respectively, for diets containing 8.1 to 11.1 MJ NE/kg; linear and quadratic, P < 0.01). The increase in dietary NE concentration was associated with an increase in dressing percentage (76.5, 77.0, 77.4, 78.0, 78.2, and 78.4% of BW; linear, P < 0.01) but no differences in lean percentage (58.3, 57.9, 58.0, 57.3, 58.1, and 56.4% of HCW, respectively, for diets containing 8.1 to 11.1 MJ NE/kg; P = 0.12). When dietary NE concentration increased from 8.1 to 11.1 MJ/kg, the G:F increased (0.326, 0.352, 0.364, 0.405, 0.425, and 0.428 kg/kg, respectively; linear, P < 0.01), but the G:F expressed using the NE system did not change (G:F, 39.97 g/MJ NE; P = 0.44). When adjusted to the same dressing yield and lean percentage, the differences in adjusted ADG increased among treatments, but the adjusted G:F expressed using the NE system was not influenced by dietary energy concentration. These results confirm the ability of individually housed pigs to adjust their spontaneous feed intake over a very wide range of NE concentrations (8.7 to 10.5 MJ/kg). Under commercial conditions, pigs may experience less variation in ADFI than the results obtained in this experiment because of differences in dietary energy concentrations. However, it seems that only a severe reduction in dietary energy concentration will be effective in restricting energy intake of pigs that are allowed ad libitum access to feed.

Analysis of factors to predict piglet body weight at the end of the nursery phase.

In pig (Sus Scrofa) production, within-batch variation in bw gain of piglets during the nursery period (up to 10 wk of age) can be high and is of high economic importance. Homogeneity of BW within batches of animals is important as it influences the efficiency of use of the grower and finisher facilities, and provides an extra value for the fattening farms. In the current study, factors for a light BW at the end of the nursery period of pigs were determined by analyzing datasets from 3 different swine research centers in the Netherlands and France. The entire dataset contained information on 77,868 individual piglets born between 2005 and 2010. Body weight was determined at different time points over the pre- and post-weaning phase, and sex, season of birth, litter information (litter size at day of birth and after cross-fostering, number of piglets born alive per litter, number of total born littermates, sow parity number), cross-fostered animals (yes or no), and pen group size over the post-weaning period were recorded. A risk factor analysis approach was used to analyze the datasets to determine factors that predict piglet bw at the end of the nursery period. Body weight at the end of the nursery period corrected for age was mainly determined by season (P < 0.001), birth weight (BiW, P < 0.001), weaning weight (WW, P < 0.001), and BW at 6 wk of age (P < 0.001). These variables were consistent among datasets and explained approximately 70% of the overall variation in BW at the end of the nursery period. Litter information did not significantly (P > 0.05) contribute to explaining the BW at the end of the nursery period. To discard the possibility of intrauterine growth retarded piglets (IUGR) being the reason for the influence of BiW as an explanatory factor in the regression model, a further analysis was performed on the effect of this category of piglets on the results of the regression analysis. Overall, it was concluded that the bw of piglets at the end of the nursery phase is mainly determined by season, sex, birth, WW, and BW at 6 wk of age. Piglets with a BiW greater than the mean biw minus 2.5 times the sd have the potential to compensate during the subsequent phases of growth.

Effect of dietary fat or starch supply during gestation and/or lactation on the performance of sows, piglets' survival and on the performance of progeny after weaning.

Two trials were carried out to compare the effects of fat or starch inclusion in sow's diet on sow and litter performance. In each trial, sows were assigned to one of two treatments. In trial 1, the sows were fed diets containing either soybean oil (5%, treatment GL5) or cornstarch (11.3%, GL0) from day 35 of gestation to weaning. Daily net energy and nutrient allowance were equalised during gestation. In trial 2, the same treatments were applied only after farrowing (treatments L5 and L0, respectively). Within each trial, a batch of piglets was studied until slaughter. In trial 1, adipose cell development and total lipid content were determined on some pigs at weaning (n = 6/treatment) and at slaughter in dorsal subcutaneous adipose tissue (n = 13/group at least) and in muscle (n = 46/group at least). Piglets' birth weight was not affected by treatment in trial 1. Survival rates at birth and after 24 h of life were higher in treatment GL5 (4.0% v. 7.5% stillborn piglets in GL0 treatment, P < 0.05; 8.7% v. 12.6% of piglets alive at 24 h of age died in treatment GL0, P = 0.06). Subsequently, overall survival rate until weaning was higher in treatment GL5 (81.4% v. 75.7% of total born piglets, P = 0.03), but litter size at weaning was not significantly affected (11.3). Litter growth rate before weaning was increased when a fat-enriched diet was provided during gestation and lactation (+140 g/day per litter; P < 0.01) and to a lower extent when provided only after farrowing (+90 g/day; P < 0.05). Energy supply through fat did not decrease the mobilisation of the sow's body reserve and backfat thickness loss was even higher with treatment GL5 (P < 0.05). After weaning, pigs' average daily gain, feed : gain ratio and carcass lean content were not affected by the energy source supplied before and/or after farrowing. At weaning, the number of adipose cells in the dorsal subcutaneous adipose tissue and in the Longissimus dorsi muscle was higher in the GL5 pigs. Muscle lipid content at weaning did not differ between treatments, but it was higher at slaughter, around 110 kg, in the GL5 pigs (3.46% v. 2.58%, P < 0.001).

Influence of some sow characteristics on within-litter variation of piglet birth weight.

Within-litter variation of piglet birth weight (BW0) is associated with an increased piglet mortality and a high variability in pig weight at weaning and weight or age at slaughter. Data collected in two experimental herds were used to quantify within-litter variability in BW0 and to assess the influence of factors mainly related to the sow. Within 24 h after birth, piglets born alive were individually weighed and stillborn piglets were collectively (first data set) or individually (second data set) weighed. The first data set was restricted to litters with no or only one stillborn piglet (3338 litters). It was used to assess the influence of genetic selection on BW0 variation by comparing litter characteristics before (1994 to 1996) and after (2001 to 2004) the development of hyperprolific sows in this herd. The second data set included all litters (n = 1596) from sows born between 2000 and 2004. For each litter, mean BW0 (mBW0) and its coefficient of variation (CVBW0) were calculated. Then, variance analyses were performed to test the influence of litter size, parity, year of sow birth and season at conception. Prolificacy improvement was associated with an increased CVBW0 in litters from pure Large White (LW) and Landrace × Large White (LR × LW) crossbred sows. The CVBW0 averaged 21% and was significantly influenced by litter size and parity. It increased from 15% to 24% when litter size varied from less than 10 piglets to more than 15 piglets. The proportion of small piglets (i.e. weighing less than 1 kg) increased concomitantly. The CVBW0 was not repeatable from a parity to the following. It was lowest for first and second parities (20%) and thereafter increased progressively. The CVBW0 was positively related to sow's backfat thickness gain during gestation. Taking into account litter size, parity, year of sow birth and season at conception explained 20% of BW0 variation. Thus, major part of heterogeneity is due to other factors, presumably including embryo genotype, on the one hand, and factors that influence embryo and foetus development, such as epigenetic factors, on the other hand.

Effects of exposure to high ambient temperature and dietary protein level on performance of multiparous lactating sows.

Fifty-nine multiparous Large White x Landrace sows were used to determine the effects of high ambient temperature and level of dietary heat increment on lactation and reproductive performance. During a 28-d lactation and the 14-d postweaning period, ambient temperature was maintained constant at 20 or 29 degrees C. Experimental diets fed during lactation were a control diet (NP; 17.6% crude protein) and two low-protein diets obtained by reduction of CP level (LP; 14.2% CP) and both reduction of CP and addition of 4% fat (LPF; 15.2% CP); the NE:ME ratio was 74.3, 75.6, and 75.8% for NP, LP, and LPF diets, respectively. All diets provided 0.82 g of digestible lysine/MJ of NE, and ratios between essential amino acids and lysine were above recommendations. During the ad libitum period (i.e., between d 7 and 27 of lactation), ADFI and NE intake decreased, respectively, from 7.63 to 4.22 kg and 82.0 to 43.3 MJ of NE when the temperature increased from 20 to 29 degrees C. Exposure to 29 degrees C reduced litter BW gain (2,152 vs 2,914 g/d) and increased lactation BW loss (34 vs 16 kg) but increased postweaning BW gain (2 vs - 4 kg). Expressed per kilogram of feed intake, water intake increased from 4.0 to 7.5 L between 20 and 29 degrees C. Compared with the NP diet, low-CP diets (LP or LPF) maintained performance and reduced total N excretion (-22.5%) in lactating sows at thermoneutrality and attenuated the negative effects of high temperature on NE intake and BW loss (40.9 vs 47.9 MJ of NE/d and 41 vs 30 kg for NP and LP + LPF diets, respectively). Temperature and diet composition did not affect the reproductive performances, and the mean weaning-to-estrus interval was 4.9 d. The respiratory rate and skin, udder, and rectal temperatures increased markedly at 29 degrees C (105 vs 33 breaths per min and 37.8 vs 36.1 degrees C, 38.9 vs 38.2 degrees C, and 39.5 vs 38.8 degrees C, respectively) without any effect of diet. In conclusion, low heat increment diets (i.e., with reduced CP/NE ratio) did not affect lactation performance of sows at thermoneutrality and attenuated the effects of high ambient temperature on energy intake and BW loss. At any ambient temperature, N excretion can be markedly reduced.

Modelling heat production and energy balance in group-housed growing pigs exposed to low or high ambient temperatures.

The effects of ambient temperature (T; 12-29 degrees C), body weight (BW; 30-90 kg) and metabolisable energy intake (ME) on components of energy balance were studied in seven groups of Piétrain x Large White barrows kept in a respiratory chamber. In Expt 1 (groups 1, 2 and 3), T varied in a cyclic way from 22 degrees C to 12 degrees C and then from 12 degrees C to 22 degrees C with three or four consecutive days at each of 22, 19, 16, 14 and 12 degrees C. Similarly, in Expt 2 (groups 4, 5 and 6), T varied from 19 to 29 degrees C and then from 29 to 19 degrees C with three or four consecutive days at each of 19, 22, 25, 27 and 29 degrees C. In both experiments, pigs were offered feed ad libitum. In Expt 3, pigs (group 7) were exposed to the thermic conditions of Expt 1 but their feed allowance was adjusted on a BW basis to the ad libitum intake recorded at 19 and 22 degrees C in Expt 1. Groups 1, 2, 4, 5 and 7 were used over two successive cycles with initial average BW of 37 kg at cycle 1 (four pigs per group) and 63 kg at cycle 2 (three pigs per group). Groups 3 and 6 were studied at an intermediary stage of growth; their initial BW was 45 kg. The O2 and CO2 concentrations, physical activity and feed intake were continuously and simultaneously measured and used to calculate total heat production (HP; HPtot), HP due to physical activity (HPact), activity-free HP (HP0), and thermic effect of feed. HP was modelled as a non-linear function with T, BW and ME as predictors. Results indicate that all components of HP were proportional to BW(0.60). Physical activity was minimal between 19 and 27 degrees C (8 % ME). The estimated lower critical temperature was 24 degrees C. Between 24 and 12 degrees C, total thermic effect of feed decreased from 31 to 16 % ME, but the short-term thermic effect of feed (5.1 % ME) remained constant. Equations for prediction of HPtot, HPact and HP0 according to BW, T and ME are proposed and evaluated according to literature values; values for the feed cost of thermoregulation in pigs are proposed.

Influence of high ambient temperatures on performance of multiparous lactating sows.

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.