In the Family Pen System piglets and fatteners grow up in species-specific family groups that correspond to the normal social organization of domestic pigs. The feasibility of a technologically improved version of this alternative housing system, originally designed by Alex Stolba, was tested on a commercial farm for two and a half years. Eighty-one litters were born in three family groups within this period. Average cycle length was 170 ± 24 (SD) days, resulting in 2.15 litters per sow per year. All piglets were suckled for at least seven weeks. In 53.8 per cent of the cycles lactational oestrus occurred before the piglets were seven-weeks-old. The litters of sows which did not show lactational oestrus were artificially weaned and returned to the family group as soon as the sow had been served. At the beginning there were problems with piglet health and crushing, but in the last 21 months of the study there was a stable reproductive performance of 19.5 piglets (28-days-old) reared per sow per year (n = 53 litters). Sows that had been raised themselves in the Family Pen System reared 21.4 piglets per year (n = 25 litters). In conclusion, the technologically improved version of the Family Pen System was found to be practicable on a commercial farm.

A trial was conducted to compare the growth performance and carcass characteristics of 720 growing pigs housed in one of three different finishing systems: outdoor paddocks, straw yards and fully slatted pens. Two genotypes were used: ‘indoor’ (progeny of Large White ✕ Landrace sows mated to Large White boars) or ‘outdoor’ (progeny of part-Duroc or part-Meishan sows, mated to Large White boars). Groups of 20 pigs were reared from an average of 30 to 80 kg live weight and given ad libitum access to a commercial specification diet. The outdoor genotypes had significantly lower average daily gain than the indoor genotype (682, 673 and 719 g respectively for part-Duroc, part-Meishan and indoor-type pigs, P 0·01). Part-Meishan genotypes had significantly higher backfat levels than the indoor genotype (P 0·05), with an intermediate value for part-Duroc pigs (22·6, 21·1 and 21·8 mm respectively). Values for food conversion ratio were significantly higher for combined outdoor genotype groups when compared with the indoor genotype (2·76 v. jt>2·62, P 0·05). Average daily gains of pigs in straw yards and outdoor paddocks were significantly higher than for those in fully slatted pens (736 and 675 v. 627 g, P 0·01 respectively). Food conversion ratio was similar for pigs in outdoor paddocks and fully slatted pens, but significantly lower for those in straw yards (2·77 and 2·75 v. 2·55, P 0·01 respectively). Backfat depth (P1 + P3 mm) was significantly greater for animals finished in straw yards compared to those in outdoor paddocks (22·2 v. 20·6 mm, P 0·05) and intermediate for those finished in fully slatted pens (21·5 mm). Interaction between finishing system and genotype did not occur to any major degree, hence it appears unnecessary to specify a particular genotype for a particular finishing system. It was concluded that pigs of the outdoor genotype had a lower growth performance compared with the indoor genotype. Finishing systems however may have been confounded by other factors so that no clear recommendations can be made as to the optimum finishing system.

This study examined the temporal relationships between behavioural activity and hormones associated with stress in gilts farrowing in two environments. Thirty-one Large White × Landrace gilts with indwelling jugular catheters were blood sampled daily (08.00 and 16.00 h) from 10 days before their expected parturition date (EPD). Five days before EPD they were moved to either a farrowing crate (C) with no bedding, or a pen (P) (2·5 m × 3·0 m) with straw provided and were blood sampled daily at 08.00, 12.00 and 16.00 h. Around 12 h before the onset of farrowing an extension was fitted to the catheter and blood samples were taken remotely at 30-min intervals. The posture of the gilts was recorded using 5-min scan samples over the 24 h pre-farrowing. The proportion of scans standing (an index of activity) was strongly affected by time (P < 0·001) with peak levels at approximately 8 h pre-farrowing in both treatments, and by treatment (0·25 v. 0·33 (s.e.d. 0·03) for C and P gilts respectively; P < 0·05). Plasma cortisol concentrations also increased before farrowing (P < 0·001) reaching a peak at 12 to 6 h pre-farrowing. Crated gilts had higher cortisol concentrations than, penned gilts (overall mean 41·5 v. 30·7 (s.e.d. 3·8) [μg/l for C and P gilts respectively; P < 0·05) at 24 to 12 (P < 0·05), 12 to 6 (P < 0·01) and 6 to 2 (P < 0·05) h pre-farrowing. Plasma ACTH concentration showed a similar pattern to cortisol over the pre-parturient period, peaking at 12 h pre-farrowing in both treatments (time: P < 0·001); crated gilts had significantly higher concentrations of ACTH at 6h pre-farrowing only (P < 0·05). Plasma β-endorphin concentrations also showed a gradual rise (P < 0·001) towards parturition; however no treatment differences were seen. These results suggest that the pituitary-adrenal (PA) axis is stimulated during pre-farrowing activity irrespective of farrowing environment. Crates, without bedding, further stimulate the PA axis over the pre-farrowing period perhaps by preventing nest-building. The rise in Q-endorphin may be involved in an endogenous defence against parturition pain.