E.H. van der Waaij

Sow line differences in heat stress tolerance expressed in reproductive performance traits

The objectives of this study were 1) to investigate if there were differences in the relation between temperature and reproductive performance traits in 2 different sow lines, a Yorkshire line producing mainly in temperate climates and a Large White line producing mainly in warm climates, and 2) to determine the upper critical temperature (UCT) for the reproductive performance of these 2 lines. Sows are exposed to heat stress when temperature exceeds the UCT of the thermo-neutral zone. Data included 32,631 observations on reproductive performance from 11,935 sows on 20 farms in Spain, collected from 2003 to 2005. Sows belonged to 2 different purebred sow lines, named D (Yorkshire sow line, producing mainly in temperate climates) and I (Large White sow line, producing mainly in warm climates). Only first insemination records per parity were used and were combined with the maximum outside temperature at day of insemination. Upper critical temperatures were studied for 3 reproduction traits: farrowing rate (0 or 1), litter size (range from 1 to 25), and total number of piglets born per first insemination (combination of farrowing rate and litter size, range from 0 to 25). Data were corrected for fixed effects, which included parity, service sire, and an interaction between farm and year. Corrected data were used as observations in the models to study the effect of outside temperature on reproductive performance. Two models were compared for goodness of fit: a linear regression model and a plateau-linear model with the plateau representing the thermo-neutral zone and a linear decrease above that zone. Farrowing rate of I-line sows was not affected by temperature. For litter size and total number born per first insemination of I-line sows no UCT could be estimated. These traits were linearly affected by temperature. For all 3 reproduction traits of the D-line the best model was the plateau-linear model; the UCT for the D-line sows was estimated to be 19.2 degrees C for farrowing rate, 21.7 degrees C for litter size, and 19.6 degrees C for total number born per first insemination. The decrease in reproductive performance of I-line sows with increasing outside temperature was less than in D-line sows. From this study it can be concluded that there are differences in heat stress tolerance between sow lines as measured by the differences in reproductive performance. These differences are an indication of genetic differences in heat stress tolerance in sow lines.

Effect of daily environmental temperature on farrowing rate and total born in dam line sows

Heat stress is known to adversely affect reproductive performance of sows. However, it is important to know on which days or periods during the reproduction cycle heat stress has the greatest effects for designing appropriate genetic or management strategies. Therefore, this study was conducted to identify days and periods that have greatest effects on farrowing rate and total born of sows using 5 different measures of heat stress. The data consisted of 22,750 records on 5024 Dutch Yorkshire dam line sows from 16 farms in Spain and Portugal. Heat stress on a given day was measured in terms of maximum temperature, diurnal temperature range and heat load. The heat load was estimated using 3 definitions considering different upper critical temperatures. Identification of days during the reproduction cycle that had maximum effect was based on the Pearson correlation between the heat stress variable and the reproduction trait, estimated for each day during the reproduction cycle. Polynomial functions were fitted to describe the trends of these correlations and the days with greatest negative correlation were considered as days with maximum effect. Correlations were greatest for maximum temperature, followed by those for heat load and diurnal temperature range. Correlations for both farrowing rate and total born were stronger in gilts than in sows. This implies that heat stress has a stronger effect on reproductive performance of gilts than of sows. Heat stress during the third week (21 to 14 d) before first insemination had largest effect on farrowing rate. Heat stress during the period between 7 d before successful insemination until 12 d after that had largest effect on total born. Correlations between temperatures on consecutive days during these periods were extremely high ( > 0.9). Therefore, for farrowing rate the maximum temperature on 21 d before first insemination and for total born the maximum temperature at day of successful insemination can be used as predictive measures of heat stress in commercial sow farms. Additionally, differences between daughter groups of sires were identified in response to high temperatures. This might indicate possibilities for genetic selection on heat tolerance.

Effect of excessive, hormonally induced intrauterine crowding in the gilt on fetal development on day 40 of pregnancy

Selection for litter size may result in an increase in uterine crowding due to a faster increase in ovulation rate than in litter size. Increased ovulation rate does not result in a proportionally increased number of piglets born alive. In this study, the effect of ovulation rate on vitality characteristics of fetal-placental units at d 40 of pregnancy was investigated. For this, 43 Large White gilts were treated with hormones to induce superovulation. Average ovulation rate was 45.16 +/- 13.22; average number of vital fetuses at d 40 of pregnancy was 17.09 +/- 3.61 that weighed 11.26 +/- 1.99 g; their placenta weighed 31.88 +/- 14.79 g; and they occupied 11.69 +/- 4.90 cm of the uterus. Loss in oocytes (i.e., that did not result in a vital fetus at d 40) increased with increasing ovulation rate and occurred before (early mortality; P = 0.0003) and after implantation (late mortality, i.e., traces visible at d 40; P < 0.0001). With respect to the vital fetuses, increased ovulation rate resulted in decreased fetal (P = 0.0008) and placental weight (P = 0.0008) and decreased length of the area in the uterus that was occupied by the placenta (P = 0.0011). Strong correlations existed between placental and fetal weight [0.68; 95% confidence interval (CI) = 0.64 to 0.72], and placental weight and length (0.78; 95% CI = 0.74 to 0.82). Fetal-placental characteristics were weakly correlated to distance to the implantation sites of neighboring fetuses, a measure of crowdedness [-0.002 (95% CI = -0.042 to 0.038) with fetal weight to 0.16 (95% CI = 0.12 to 0.20) with placental length]. Increased ovulation rates, but more specifically increased late mortality rates, have negative effects on the remaining vital fetuses with respect to the fetal (P = 0.0085) and placental weight (P < 0.0001) and length of the implantation site (P = 0.0016). The most extreme effect was on placental weight, in which a uterus with <10 cases of late mortality was on average 25% greater than placental weight in a uterus with >18 cases of late mortality (P < 0.0001). Furthermore, increased ovulation rates resulted in decreased within litter variation for fetal (P = 0.0018) and placental weight (P = 0.0084). At increased ovulation rates, the number of live fetuses remained similar, but placental development is impaired and the growth of the fetus is retarded compared with reduced ovulation rate, with effects likely lasting into adult life.

Effect of match or mismatch of maternal-offspring nutritional environment on the development of offspring in broiler chickens

In mammals, maternal food restriction around conception and during pregnancy results in low birth weight and an adjusted growth trajectory of offspring. If, subsequently, the offspring are born into a food-abundant environment, they are at increased risk of developing obesity, type 2 diabetes, hypertension and renal dysfunction. Here, we show similar effects of maternal undernutrition on hatch weight, growth and fat deposition in offspring of birds (domestic chicken). Both mothers and offspring were fed either ad libitum or restricted in a two-by-two factorial design, resulting in two matched and two mismatched maternal-offspring nutritional environments. Offspring of ad libitum mothers grew heavier than those of restricted mothers, possibly due to the larger muscle mass. Ad libitum-fed offspring, especially females, of restricted mothers were lighter at hatch, and were heavier and had more abdominal fat at 6 weeks of age than daughters of ad libitum-fed mothers. These results suggest a common mechanism in mammals and birds in response to a mismatch in the maternal-offspring nutritional environment. They also indicate that the common practice of restrictive feeding of the broiler breeders and subsequent ad libitum feeding of the broilers may result in reduced growth and increased abdominal fat as compared to broilers of less restricted broiler breeders.

High natural antibody titers of indigenous chickens are related with increased hazard in confinement

Natural antibody (NAb) levels and survival rates were evaluated in 4 breeds of laying hens in Ethiopia: indigenous, improved indigenous, exotic layer, and crossbred. Titers of NAb isotypes IgG and IgM binding keyhole limpet hemocyanin (KLH) in serum were measured at 20, 26, 35, and 45 wk age. Repeated-measure ANOVA showed that IgG and IgM levels vary with time within each breed (P < 0.05). Indigenous chickens had significantly (P < 0.05) higher NAb levels at all ages. The Cox proportional hazard analysis showed increased hazard with increased levels of NAbs in the exotic layers (P < 0.05). However, the reduced hazards with increased levels of NAbs were not significant in the improved indigenous and crossbred chickens. Indigenous chickens showed increased hazard with increasing levels of NAb (P > 0.05). We concluded that not only the NAb levels but also the effect of Nabs on survival vary between indigenous and improved breeds. The results indicate that NAb levels are associated with survival in elite (improved) breeds, but are associated with increased hazard in indigenous chickens.

Indigenous chicken genetic resources in Kenya: their unique attributes and conservation options for improved use

The indigenous chicken (Gallus gallus domesticus) genetic resources (IC) comprise more than 80% of the overall poultry population in rural villages despite their low productivity. However, a holistic approach that increases productivity without increasing production costs or leading to loss of biodiversity is presently limited. Conversely, in most developing countries, there is almost no organizational structure for breeding programmes for improving and conserving IC. These locally adapted IC can only be conserved in the most rational and sustainable way by ensuring that they are functional part of different production systems. Their conservation should be through utilisation if they are to be of any benefit to the poor rural households. This discussion focuses on five very relevant questions that need to be answered if the conservation of IC is to be effective and sustainable: What, why and how should we conserve, who are the stakeholders and what are their roles in conservation efforts?

The N'Dama cattle genetic improvement programme: a review

1International Trypanotolerance Centre, PMB 14 Banjul, The Gambia 2Wageningen Institute of Animal Sciences, PO Box 338, 6700 AH Wageningen, The Netherlands 3Department of Farm Animal Health, Veterinary Faculty, University of Utrecht, P.O. Box 80151, 3508 TD, Utrecht, The Netherlands 4Technical University Munich, Department of Animal Science, D-85350 Freising-Weihenstephan, Germany 5 United Data Systems for Animal Production (VIT), Heideweg 1, D-27283 Verden, Germany

Morphological features of indigenous chicken ecotype populations of Kenya

This study characterized indigenous chicken (IC) ecotypes morphologically. Five IC ecotypes studied were Kakamega (KK), Siaya (BN), West Pokot (WP), Narok (NR) and Bomet (BM). Data on morphological features were collected from 1 580 chickens and 151 for zoometric measurements. Descriptive statistics, non-parametric and F tests were used in analysis. A non-parametric Kruskal–Wallis, Binomial test and Mann–Whitney U test was used to evaluate whether the ecotype have effects on the qualitative morphological variables. Zoometric measurements was analysed with the PROC GLM of SAS. Results revealed that, black, black-white striped, brown and red body plumage colours were significantly different (P 0.05). Distribution of body feathers (%), comb types (%) and zoometric measurements were significantly different (P <0.05). Eye colours varied significantly (P <0.001) within the ecotypes unlike between the populations. In conclusion, IC ecotypes studied are heterogeneous population with huge variability in morphological features.

Adoption of exotic chicken breeds by rural poultry keepers in Ethiopia

Abstract This study examines factors that determine the probability and intensity of adoption of exotic chickens among rural poultry producers in Ethiopia. A total of 240 respondents were interviewed from households that were selected by systematic random sampling. The differences between adopters and non-adopters were identified using descriptive statistics. Factors that affect the probability and intensity of adoption were identified using the Heckman selection two-step model. Adopters of exotic chickens had more social contact and less livestock income than non-adopters. Additionally, adopters had access to an off-farm income and credit and considered exotic chickens easier to manage than non-adopters (p < 0.001). In the econometric analysis, the probability of adopting exotic chickens was found to be positively affected by access to an an off-farm income (p < 0.01) and negatively by livestock income (p < 0.05). The intensity of adoption was negatively affected by being male household head (p < 0.001), having a larger farm size (p < 0.01), and having livestock income (p < 0.05).

Effect of gestating sow body condition, feed refusals, and group housing on growth and feed intake in grower-finishing pigs.

The main focus of this study was to identify sow gestation features that affect growth rate (GR) and feed intake (FI) of their offspring during grower-finishing stage. Because the sow provides a specific environment to her offspring during gestation, certain features (e.g., BW of the sow), feed refusals or gestation group, may affect her ability to deliver and feed a healthy litter. Data on 17,743 grower-finishing pigs, coming from 604 sires and 681 crossbred sows, were obtained from the Institute for Pigs Genetics. Sow gestation features were collected during multiple gestations and divided into 3 clusters describing i) sow body condition (i.e., BW, backfat, and gestation length), ii) sow feed refusals (FR), the difference between offered and eaten feed during 3 periods of gestation: 1 to 28, 25 to 50, 45 to 80 d, and iii) sow group features (i.e., number of sows, and average parity). Sow gestation features were added to the base model 1 at a time to study their effect on GR and FI. Significant gestation features (P < 0.1) were fitted simultaneously in animal model to investigate whether they could explain common litter and permanent sow effects. Gestation length had effect on GR [1.4 (g/d)/d; P = 0.04] and FI [6.8 (g/d)/d; P = 0.007]. Body weights of the sow at insemination [0.07 (g/d)/kg; P = 0.08], at farrowing [0.14 (g/d)/kg; P < 0.0001], and after lactation [0.1 (g/d)/kg; P = 0.003] had effect on GR. Sow parturition-lactation loss in backfat thickness and weight were not significant for GR and FI. Days with FR during 25 to 50 and 45 to 80 d of gestation and average FR during 45 to 80 d of gestation had negative effect on GR and when substantially increased had also a positive effect on FI. Sow FR from 1 to 28 d of gestation were not significant. Number of sows in gestation group had effect on FI [-9 (g/d)/group member; P = 0.04] and day sow entered group had an effect on GR [-0.9 (g/d)/day; P = 0.04]. Sow gestation features explained 1 to 3% of the total variance in grower-finishing pigs. Gestation features did explain phenotypic variance due to permanent sow and part of phenotypic variance due to common litter effects for FI but not for GR.