The aim of this study was to assess the effect of grazing (G) vs. zero-grazing (ZG), level of milk production, and quality and type of housing system [free stalls (FS) and straw yards (SY)] on the prevalence of lameness and leg injuries in dairy cows. Observations were made on 37 commercial dairy farms across Great Britain. A single visit of 5 d duration was made to each farm. During this visit, lameness scores and the incidence of swellings, rubs, and injuries to hocks and knees were recorded on all the peak- or mid-lactation cows. Aspects of the quality of housing and management that were likely to affect foot and leg health were recorded. There were more lame cows on ZG farms (39 +/- 0.02%) than on grazing (G) farms (15 +/- 0.01%), and lameness scores were higher on FS farms compared with SY farms (0.25 +/- 0.01 vs. 0.05 +/- 0.01). Cows on SY farms had fewer hock and knee injuries compared with FS farms. The frequency of knee swellings was higher on ZG farms (0.31 +/- 0.02) than on G farms (0.15 +/- 0.01). Aspects of the free-stall design affected foot and leg health. The number of hock swellings increased with increasing stall gradient (0.16 +/- 0.01 with no slope vs. 0.39 +/- 0.02 at a 0 to 1.5% slope). There was an interaction between the length of the free-stall lunging space and the hip width of the cow, indicating that the incidence of lameness is generally highest on farms with small free stalls and heavy cows. High levels of milk production did not affect lameness or leg injury. The results indicate that housing cows throughout the year potentially has a detrimental effect on foot and leg health. However, good free-stall design may reduce lameness and leg lesions.

Environmentally induced stereotypies, commonly observed in farm and zoo animals, are behaviors that are relatively invariant, that are regularly repeated, and that serve no obvious function. However, there is as yet no accepted means of discriminating between normal and abnormal behavior, and the assumption that stereotypies are abnormal may mask the fact that they arise in part through processes that "normally" control behavior. There is growing evidence that stereotypies in sows and broiler breeders are strongly related to feeding motivation. For example, sows only develop oral stereotypies if their feed intake is restricted, and operant conditioning experiments have shown commercial levels of feed restriction to give rise to high levels of feeding motivation. Stereotypies in animals whose feed intake is restricted largely occur in the postprandial period, and ingestion of food has specifically been shown to elicit stereotypies in sows. These observations suggest that positive feedback from feeding produces a short-term increase in feeding motivation that at the end of the meal is directed toward available, alternative stimuli such as chains, the choice of stimuli reflecting the sensory feedback from the activity. Drinking behavior may also become an expression of feeding behavior after metabolic water requirements are met. In addition to these processes specific to feeding motivation, it seems likely that nonspecific processes, which operate more generally across motivational systems, contribute to the persistence of the behavior. Behavioral arousal may facilitate performance of active behaviors, and sensitization of the underlying neural elements may lead to the behavior being more easily elicited and maintained. A crucial factor in the sensitization process would seem to be the channeling of complex behavior by the environment into a few and very often repeated sequences of behavior. This approach suggests that stereotypies can be prevented by either reducing the level of motivation underlying the stereotypy, or by allowing for the expression of more complex behavior and thereby preventing the processes of channeling and sensitization from occurring.

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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.

As a part of a study investigating the extent to which ad libitum feeding of a high fibre diet could mitigate behavioural problems associated with food restriction, the performance of sows given food at restricted or ad libitum levels was compared. Ten subgroups of five were allocated to each of the restricted (R) and ad libitum (A) feeding regimes. Five weeks after service, subgroups were introduced into one of two dynamic groups of sows housed in adjacent straw-bedded pens. R sows received a fixed daily ration (parity 1: 2·2 kg; parity 2: 2·4 kg) of a conventional pregnancy diet (13·1 MJ digestible energy per kg) from an electronic sow feeder. Sows on the A regime had unrestricted access to five single-space hoppers dispensing a high fibre diet (containing 600 g unmolassed sugar beet pulp per kg). Subgroups were maintained on these gestation feeding regimes for two consecutive parities. During both parities, A sows were heavier by day 50 of gestation (parity 1: P < 0·05; parity 2: P < 0·01) and at farrowing (parity 1: P < 0·001; parity 2: P < 0·001) than R sows. No difference was found between feeding regime in sow weight at weaning, due to a greater weight loss during lactation of A (parity 1: P < 0·001; parity 2: P < 0·001) than R sows. No difference was found between feeding regime in sow backfat thickness, sow reproductive performance or litter performance in either parity. This suggests that unmolassed sugar beet pulp diets may be used to feed sows on an ad libitum basis during gestation without compromising productivity. However, food intakes may be too high (estimated at 4·1 kg per sow per day) to make ad libitum feeding of pregnant sows an attractive option for producers.

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