Search

Eighteen of 23 red deer (Cervus elaphus) at a deer slaughtering premises were successfully stunned with an apparatus modified from that normally used to stun sheep. The five unsuccessful electrical stuns were associated with poor head restraint and poor head contact by the electrodes. The median stunning current was 0.9 A, and in the majority of cases the duration of stunning was less than 1 second. The signs of the electrically induced epileptiform seizures in the deer were dissimilar to those seen in sheep, cattle and pigs, in that the initial tonic phase was less marked, and of shorter duration. A similar shorter and less obvious tonic phase was noted in four deer shot with a captive bolt pistol. Two animals which were electrically stunned, and bled within 10 seconds, showed no signs of recovery while bleeding. The electroencephalograms of four deer stunned with currents of 1.3 A for a duration of either 0.5 or 1.0 seconds were recorded under more controlled conditions. All four animals developed electroencephalograms typical of an epileptiform seizure. The animals exhibited behavioural reactions similar to the other 18 animals in the trial at the deer slaughtering premises and were rendered unconscious for between 54 and 122 seconds. The electroencephalogram activity amplitude was greater than that recorded immediately before stunning and took between 6 and 9 seconds to build up to maximum value. It is concluded that, providing the heads of deer are adequately restrained, head-only electrical stunning can be incorporated into a humane method of slaughter for deer.

Passing an electric current (50 Hz, 400 V open circuit, current limited to 1.5 A) from two electrodes acting as a common single electrode set applied on each side of the dorsal surface of the neck (cervical vertebrae C2 to C5 region) to another placed on the brisket of young bulls causes fibrillation of the cardiac muscle, does not induce epileptiform changes in the electroencephalogram, and produces a state of body rigidity. Passing the same electric current through the same neck electrodes, now acting as two separate electrodes, without the brisket electrode, does induce epileptiform activity similar to that seen with head-only stunning, does not fibrillate the heart, and produces a state of limb rigidity lasting for some time after the stun. Given that the presence of epileptiform activity is a criterion for effective electrical stunning and is indicative of insensibility, neck-to-brisket stunning as described here does not appear to be humane.

This paper examines the role of the vertebral arteries of calves in determining the time to loss of spontaneous electrocortical activity after slaughter by a throat-cut severing the soft tissues of the neck ventral to the spinal column. Four calves with the vertebral arteries ligated took 43 +/- 1.3 s to lose cortical activity after the throat was cut. Four similar animals with intact vertebral arteries and the rostral end of the common carotid arteries clamped immediately after slaughter, to ensure that vertebral blood passed to the brain, took 51 +/-25 s to lose cortical activity. It was concluded that factors other than blood flow from the vertebral arteries contribute to the prolonged time to loss of electrocortical activity after slaughter that has been observed in some calves.

Electroencephalographic (EEG) recordings were made on 34 calves (two days to six weeks old, 30-50 kg) during the slaughter process. The calves, supported in a V-shaped box or polypropylene net, were either head-only electrically stunned (50 Hz, 1.0 A) across the head and allowed to recover, head-only stunned followed by throat cutting or head-only stunned followed by throat cutting and electro-immobilisation. All time intervals were measured from the commencement of the stun. The electro-immobilisation (80 V peak, 14.3 Hz, 5 ms square wave) at 15-26 seconds post-stun was applied through electrodes attached to nose and anus, for periods ranging from 5-60 seconds. The head only stun produced an elevated EEG amplitude of the electroplectic fit which lasted approximately 34 seconds followed by a quiescent period before the EEG amplitude again became elevated above normal. A normal pre-stun pattern was not reached until many minutes had elapsed. Following the stun, the forelegs were usually flexed and then extended, gradually becoming part of the paddling movements commencing as early as eight seconds post-stun. Such movements were taking place while the animal was still stunned. With a head-only stun followed by throat cutting, the electroplectic fit was reduced to about 23 seconds and the amplitude of the EEG fell to about 10 microV after 50-73 seconds and breathing was inhibited for at least 20 seconds after stun commencement. If inadvertently only one carotid was severed, the EEG did not fall as rapidly as when both carotids were cut. The increase in amplitude of the EEG tracings was caused by stunning but the reduced duration of this increase in calves in which the throat was cut, suggests that there is an impairment of recovery of brain function from the moment of cutting and recovery of sensibility is unlikely. In reviewing the criteria of sensibility, we believe that insensibility can be presumed to continue from stun initiation, through the throat cut until the EEG falls below 10/microV provided that there is no resurgence of activity and the EEG amplitude continually falls rapidly enough. By this criteria, calves which are electrically stunned and rapidly exsanguinated remain permanently and irreversibly insensible. The addition of at least 15 seconds electro-immobilisation causes an even more rapid fall in the amplitude of the EEG (<10 microV at 50 seconds) making insensibility more certain as well as abolishing animal movement.

Twelve adult cattle were electrically stunned head-only (400 V, 2.5 A, 50 Hz) behind the ears for four seconds. Within ten seconds of stun initiation, the carotid arteries, jugular veins, trachea and oesophagus were severed. Twenty seconds after the stun initiation, ten animals received an electro-immobilization current (80 V peak, 14.3 Hz, 5 ms square wave, 300 mA) nose to anus for periods ranging from 30-37 seconds. Electroencephalographic (EEG) traces were recorded before and after the stun up until electroimmobilization and at cessation of electro-immobilization by means of implanted electrodes, and animal movement was recorded on videotape. Before the stun, the EEG trace was within a window of sensibility (10-40 microV amplitude). During the stun, the amplitude increased and sometimes exceeded 500 microV. At the end of electro-immobilization, EEG amplitude was less than 10 microV, indicating insensibility. This amplitude was reached in the two non-immobilized animals 57 seconds and 63 seconds after stun initiation. During stunning, the forelegs and hindlegs usually tucked under the animals. Various degrees of foreleg extension then occurred. From about ten seconds post-stun, paddling movements occurred, at which time the EEG trace showed large-amplitude waves characteristic of a stunned animal. During immobilization, the animals stiffened and breathing stopped. After immobilization weak muscle spasms occurred that did not interfere with dressing operations. Non-immobilized animals moved excessively, inhibiting dressing. It is concluded that adult cattle rendered insensible by stunning do not recover sensibility during the stun/throat-cut/immobilization operation and therefore this procedure is humane.