WPSA has played a pivotal role over the past 100 years in facilitating the development of the global poultry industry through the organization of branches in member countries and forums to identify and discuss issues, problems and their solution, as well as structures to disseminate that information. In this manner, WPSA has, since 1956, contributed significantly to the development of the Australian poultry industry. The Australian poultry industry has benefitted greatly over the years as a result of a well-supported and high quality national poultry research programme, facilitated through close cooperation between the poultry industry itself, national and state governments, and the country's research and education institutions.In response to the major projected increase in poultry meat and egg production and consumption in developing countries, WPSA has focussed increasing attention on facilitating efficient, sustainable and socially equitable poultry production in these countries. Associated with this, WPSA and WVPA are working towards a closer degree of cooperation and collaboration.

Small-scale family poultry farming involving semi-scavenging flocks of mostly indigenous breed poultry in rural regions of many developing countries contributes in a very meaningful way towards the social and financial needs of rural families. While productivity is relatively low, so too are inputs; which makes the production system reasonably viable, as evidenced by the many millions of such flocks worldwide. The principal constraint to profitability is the high mortality rate in young chicks, due to a combination of disease, predation, malnutrition and climatic exposure, combined with moderate to high mortality rates in grower and adult stock due to the effects of disease, of which Newcastle disease is a common cause. Simple cost-effective interventions, involving vaccination of the flock against Newcastle disease with heat-tolerant vaccines combined with early confinement of the chicks with the hen and creep feeding over the first three to four weeks, have been demonstrated to impact dramatically on survival of the birds and on household food security and profitability. Such improvements are fully compatible with programmes aimed at development of the commercial poultry meat and egg industries in developing countries to meet the needs of the urban and peri-urban populations. Family poultry-raising is experiencing a resurgence in many 'developed' countries. The number of families raising backyard poultry is on the increase due to both a growing enthusiasm for organic poultry products and the economic downturn. Backyard production systems vary in accordance with local government regulations, producer preferences, household residential circumstances and climatic conditions.

The study was conducted as a completely randomized design, with a factorial arrangement to determine the response of commercial broilers to choice feeding and limiting amino acids on growth and carcass performance. A total of 432 male birds were weighed at one-d-old and randomly distributed to 48 wire-floored brooder cage each 1.0 m(2). There were 2 sexes and 4 dietary treatments with 6 replicates each of 9 birds. Birds were given one of three dietary regimens with dietary change every 7 days. All groups were fed free choice of summit and dilution diets. The estimated dietary level of crude protein at day-old was 240 g/kg and the level at 42 d was either 120, 150 or 180 g/kg for females or 130, 160 and 190 g/kg for males. At 43 d of age, all birds from each dietary treatment were slaughtered for measurement of body composition. Results reveal that lysine requirement for maximum gain in this study was higher than NRC recommendation. The free choice-fed bird was significantly higher, in terms of growth and body composition than that obtained on the low dietary protein regimen.

An experiment with 480 day-old chicks of four commercial strains was conducted to study theeffect of genotype on response in body composition to variation in dietary protein: energy ratios. Thechicks were randomly allocated into 4x2x4 factorial and fed on a commercial starter diet (250 g CP and12.5 MJ of ME /kg) from hatching to 5 d of age and divided into two groups with three replicationseach of 16 birds and given either the such starter diet (S) or a finisher diet (F) containing 190 g CP and13.0 MJ of ME /kg. The birds were reared in strain-and sex-intermingled groups in brooders and followoncages until they reached the target body weight of 600-650 g (females) or 650-700 g (males) andtransferred to single cages and fed S or F diet until 1200-1300 g (females) or 1300-1400 g (males). Thelighting program was 23 h light for the first two days, and reduced to 18 h/d for the remainder of theexperiment. There were considerable variations in relative growth performance, FCR, carcass fat andabdominal fat due to genotypes and dietary regimen. Although birds tend to response in similar waywhen dealing with the excesses and insufficient supply, the nutrient requirements in relation to theprotein: energy ratios should be designed according to genetic background.The accumulation of fatduring the growing period was primarily due to the genetic variation whereas beyond this age, variationin abdominal fat was due principally to dietary effects.

An experiment imposing the multi continuous phase feeding was carried out to evaluate the EFG(Emman, Fisher and Gous) Growth Model in its capacity to predict amino acid requirements in broilers.Birds were fed using blended summit (247.91g/kg CP, 3200 kcal of ME /kg) and dilution (166.26 g/kgCP, 3200 kcal of ME g/kg ) diets and offered to 2-4 or 8 phases. Two hundred male day-old broilerchicks of two commercial strains (A=Ingham and B = Steggles) were used. The predicted responseswere greater than the observed both gain (g/d) and feed intake (g/d). The discrepancy between theobserved and predicted gain in the strain A and B birds, showed a different pattern, with a markeddifference during the early growing period, with a degree of convergence in the late growing period forthe strain A but the reverse picture for the strain B. This shows that strain characterization is notaccurate due to an inadequate definition of the genotypes by the model. Non agreement betweenpredicted and determined gain and feed intakes provided little benefit in moving towards a morefrequent change in diet to accommodate predicted growth-related changes in amino acid requirements.

Networks to support family poultry production systems have been ongoing for around 30 years. This paper identifies the main groups involved and details their work. The future role of the work of the networks was examined during a participatory workshop held with professionals from the networks at the World Poultry Congress 2008. Workshop participants agreed that family poultry contribute significantly to the lives of millions of poor households throughout the world and made a commitment to advance 'Poulet sans Frontieres!'The paper recommends that an overarching network is required that would provide a forum for scientist information exchange, development of standard protocols and subsequent comparison of results. This network would also speed the dissemination of results and technologies identified to improve poultry production, which can then be passed to poultry keepers. WPSA was identified as the lead organisation for a new network in concert with a number of the networks and agencies closely involved (INFPD, IRPC, DNSP and FAO). It is envisaged that these proposals would be available for discussion by the small-scale family poultry farming (SSFPF) community in 2009.

The objective of this work was to study the protein utilization and protein turnover of different broilerstrains and was carried out in completely randomized design. One hundred and forty four sexed doc fromeach strain (Cobb =A, Ingham = B and Steggels = C) were divided into a factorial arrangement (threedietary protein, two sexes and three strains). Two regimens of composite mixes of a summit and dilution dietand a free choice between these two diets. Diets were changed weekly, with notional crude protein levelsat one day-old of 240g/kg for all chickens, and at 42 days of age of 120 or 180 g/kg in the low and highprotein. Protein utilization efficiency (PRE) was measured from 39-42 d of age. PRE increased with theincreasing of dietary protein in strains A and C and had much higher response than in strain B. The moisture:protein ratios were 2.51, 2.65 and 2.58 in strains A, B and C, indicating strain B contained higher moistureand body fat and less protein. Involvement of genetic controls as the selection effect seems to increase thecapacity of chickens in improving nutrient utilization

Village poultry make a significant contribution to poverty alleviation and household food security in many developing countries. This contribution by village poultry to livelihoods can also support HIV/AIDS mitigation and wildlife conservation initiatives. Appropriate interventions focussing on the factors limiting productivity of the different production systems must be tailored according to country and local conditions. The contrast between the type of support in relation to the production systems that might be promoted in export-oriented countries such as Thailand, in comparison to others such as Mozambique and Lao PDR is discussed. A review of the benefits and costs of inputs comparing small scale commercial poultry and scavenging village poultry production systems in different countries taking into account the bio-risks for each production system demonstrates the overall efficiency of the village production system and provides an insight into why this system has continued to thrive into the 21st century.

1. Protein utilisation and turnover were measured in male chickens sampled from a line selected for high breast yield and a randombred control line (lines QL and CL, experiment 1) and in male chickens sampled from lines selected for either high or low abdominal fatness (lines FL and LL, experiment 2). In each experiment, 18 birds per line were given iso-energetic (12.9 MJ ME/kg) diets containing either 120 or 220 g CP/kg from 21 to 29 d (experiment 1) and 33 to 43 d (experiment 2).2. Measurements were made of growth rate, food intake, body composition, excreta production and N-tau-methylhistidine excretion as a measure of myofibrillar protein breakdown, and fractional rates (%/d) of protein deposition, breakdown and synthesis were calculated.3. In experiment 1, there were no significant differences between the line means for the fractional measures of protein turnover, but there was marked differential response in the two lines in the fractional rates of protein deposition, breakdown and synthesis, to increase in protein intake. The positive slope of the regressions of fractional (%/d) protein deposition and synthesis rates on protein intake (g/d/kg BW) were approximately 1.4- and 2.0-fold higher respectively in the QL than the CL line birds, and the negative slope of the regression of fractional breakdown rate on protein intake was approximately threefold greater in the CL than the QL line birds.4. In experiment 2, fractional deposition rate was 6.2% lower, but fractional breakdown rate 9.4% higher in the LL than the FL birds, whilst there was essentially no difference in response of the FL and LL birds in the components of protein turnover to increase in protein intake. Line differences in deposition and breakdown rates were thus a reflection of the considerably higher (20%) food and hence protein intake in the FL than the LL birds.5. The differential line responses in protein turnover in the two experiments suggest that selection for increased breast muscle yield and for reduced body fatness manipulate different physiological pathways in relation to protein turnover, but neither selection strategy results in an improvement in net protein utilisation at typical levels of protein intake by birds on commercial broiler diets, through a reduction in protein breakdown rate.

The effect of dietary protein supply on muscle development and circulating concentrations of insulin-like growth factors (IGF)-I and -II was examined in chickens selected for increased breast yield and decreased fatness (quality, QL) and in its control line (CL). CL and QL chickens were fed isoenergetic diets containing 121.5 or 215.8 g CP/kg during a 12-d period; comparisons were performed at 33 d of age. Birds given the high protein diet grew faster, ate less feed, had lower feed conversion ratio (FCR), and higher muscle weights than their counterparts given the low protein diet. The muscle weight response to protein supply differed between muscles in both lines, with pectoralis major appearing more sensitive than sartorius. The response of the gastrocnemius muscle depended on the line. Selection for carcass quality increased (P < 0.01) body weight, growth rate, feed intake, pectoralis major and sartorius muscle weights, and pectoralis major muscle proportion. There was, however, no line difference in FCR or in sartorius muscle proportion. The weight and proportion of the gastrocnemius muscle were higher (P < 0.05) in the QL than the CL chickens on the high protein diet, but there was no line difference for the low protein diet. Plasma levels of IGF-I, and to a lesser extent IGF-II, were lower (P < 0.01) in protein-restricted chickens. No difference in circulating IGF-II was observed between the lines. Concentrations of IGF-I were higher (P < 0.05) in QL than CL chickens, which may contribute to improved body composition for this genotype.

The efficacy of exogenous IGFs to stimulate growth and modulate protein and fat deposition was examined in a number of broiler chicken lines. From around 600 g body weight the chickens received a continuous infusion of vehicle (0.1 M acetic acid), human recombinant IGF-I or [Gly1]IGF-II at 300 microg/kg body weight per day, or a combined infusion of 150 microg/kg/day of each IGF for 2 weeks. Experiment 1 used commercial broiler female chickens and included measurements of nitrogen balance, Ntau-methylhistidine excretion and muscle protein synthesis rates. In Experiment 2 the same treatments were applied to three experimental lines of chickens selected for high food consumption (relatively fat), high food utilisation efficiency (relatively lean), or at random (control). IGF-I, but not IGF-II, significantly increased growth rate and food utilisation efficiency by around 10-15% in each experiment, an effect which was consistent across all genotypes. Nitrogen balance was significantly increased by IGF-I in Experiment 1 as was carcass nitrogen content in Experiment 2, indicating that the increased growth was in lean tissue. Carcass fat was consistently reduced in chickens receiving IGF-I and was related to the levels of circulating IGF-I (r2 = 0.30, P < 0.01) but not triiodothyronine. Protein synthesis rates were unaffected by treatment and could not account for increased growth rate. However, there was a significant reduction in Ntau-methylhistidine excretion indicating a reduced rate of muscle protein breakdown in IGF-I-treated chickens (1. 56%/day vs 2.05%/day for IGF-I-treated vs controls, P < 0.05). The efficiency of feed utilisation was inversely related to the rate of protein breakdown (r2 = 0.25, P < 0.01). In conclusion, these experiments are the first to report an enhancement of growth and food utilisation efficiency by broiler chickens receiving exogenous IGF-I. Our results show that IGF-I may be important in controlling the growth and efficiency of food utilisation of young chickens at least in part by modulating the rates of protein breakdown.

1. The inheritance of, and genetic and phenotypic correlations between, plasma insulin-like growth factor-I (IGF-I) and 28-(28dW) and 56-d (56dW) body weight, 28- to 56-d body weight gain (BWG), food intake (FI), food conversion ratio (FCR) and abdominal fatness (AF) at 56 d were determined by sib analyses in a population of 327 pedigreed progeny produced by matings between 18 cockerels and 72 pullets from a broiler strain of chickens bred at random for 8 generations. 2. Plasma IGF-I was measured in fed (IGF-If) and fasted (IGF-I) birds at 42 d. 3. Heritability estimates (sire + dam) were: 28dW 0.35 +/- 0.11, 56dW 0.49 +/- 0.13, BWG 0.51 +/- 0.13, FI 0.55 +/- 0.13, FCR 0.73 +/- 0.14, AF 0.49 +/- 0.13, IGF-If 0.10 +/- 0.08, IGF-Is 0.08 +/- 0.08. 4. The low heritability estimates with their high standard errors for the IGF-I measures precluded the calculation of meaningful genetic correlations between these and the performance traits. There were moderate to strong positive genetic correlations between 28dW, 56dW, FI and AF.

1. Rates of muscle protein turnover, growth, and food consumption were determined in 4 lines of chickens selected for either weight gain (line W), food consumption (line F), efficiency of food conversion (line E), or at random (line C) and in two Australian commercial broiler strains (S and H). These measures were related to body composition and the circulating concentrations of plasma growth hormone (GH) and IGF-I. 2. N tau-methylhistidine excretion was 10-14% higher in line F and 7-13% lower in line E compared to line C, showing divergence in the rate of muscle protein breakdown with selection. 3. There were no differences between the 4 experimental lines (W, F, E and C) in muscle protein fractional synthesis rates, whether calculated from N tau-methylhistidine excretion or measured directly by 3H-phenylalanine incorporation. 4. No consistent differences were found between lines in circulating concentrations of either GH or IGF-I but plasma IGF-I concentrations were positively correlated over all lines with protein accretion rates. There was a strong inverse correlation over all lines between the rates of protein degradation and FCR. 5. The correlated responses in protein degradation rates are consistent with the notion of a positive genetic association between the overall efficiency of food utilisation for growth and the efficiency of protein metabolism.

1. The effect of increasing dietary calcium from 10.3 to 20 g/kg on 5- to 17-day growth performance and plasma minerals, electrolytes, total protein, albumin and glucose in chickens from 4 lines selected for: high 8-week body weight (W), low abdominal fat (L), high abdominal fat (F) or at random (C) was studied in two experiments. 2. High dietary calcium significantly reduced weight gain and plasma phosphate and potassium but increased food:gain ratio, plasma total calcium, glucose and albumin. 3. Significant correlations were found between plasma total calcium and plasma phosphate (r = -0.5, P less than 0.01), plasma total calcium and protein (r = 0.4, P less than 0.01) and between plasma total protein and albumin (r = 0.55, P less than 0.01). 4. Genotypes differed in their response to dietary calcium content. There was a substantial response in line F but little effect in line L. 5. In contrast to the three other lines, in line F high dietary calcium significantly increased plasma ionised calcium without altering plasma phosphate or total calcium concentration. 6. It was concluded that genetic selection has produced lines which vary in their tolerance to high dietary concentrations of calcium. Birds selected for increased fatness were less tolerant to high dietary calcium than their lean-selected counterparts.