A biotelemetry system is described for obtaining, transmitting and recording the electromyograms (EMGs) produced in muscle activity of free-swimming fish as quantitative indicators of overall fish activity. The radiotransmitters used come in the form of cylindrical packages having two sensingelectrodes, all fully implantable in the fish body cavity. EMGs are transmitted as radio pulses with the intensity of muscular activity determining the intervals between pulses. The packages also contain temperature sensors and fish temperatures are transmitted with every 32nd pulse. Transmitted EMG pulses are detected, ' measured ' and stored by a single portable receiver (Model SRX-400, Lotek). Data can be subsequently transferred to a computer (which can also be portable) for storage, processing and statistical analysis. Transmitter battery life can be in excess of 7 months, permitting laboratory or field studies of long duration. Transmitter package implantation surgery requires a mid-ventral incision and internal securing of transmitter and sensing electrodes. Surgical silk, cyanoacrylate tissue adhesives, and polydioxanone (PD), a synthetic absorbable suture, were all tried as means of incision closure. The most effective was PD alone. Trials of the system consisted of forced swims by transmitter-equipped rainbow trout Oncorhynchus mykiss Walbaum. The data obtained provided an inverse linear relation between forced swim speed and EMG pulse interval. Trials were conducted at intervals over periods up to 2 months. Fish showed neither distress, nor difficulty in swimming up to maximum speeds of 60 cm s -' (fish lengths 41 .O, 44.4 cm).
One male and one female lake trout, Salvelinus namaycush, were held in a laboratory tank simulating a natural spawning environment. Their behaviour during their reproductive period was videotaped each day for 2 h at dusk. The fish activities were classified into seven types: resting, casual swimming, side-thrusting, chase, chase-nudge, body alignment, shuddering. As the reproductive period progressed the fish became more generally active with a marked increase in interactive behaviours such as pursuit of the female by the male (chasing, chasing-nudging). Around spawning time, shuddering and body alignment activity reached a peak. Each fish was equipped with an internally implanted radiotelemetry package able to detect and transmit continuously over the course of each day signals that reflect production of the electromyograms (EMGs) that accompany fish axial muscle activity (high muscular activity gives low pulse interval times in milliseconds). The lowest EMG pulse intervals corresponded with what, from the video records, appeared to be the time of highest physical activity during the reproductive period-viz. that associated with spawning activity during dusk. Other times during the diel cycles over the reproductive period, except for times of roughly similar duration during early morning (which may also be reflections of spawning) showed considerably lower muscular activity. It is concluded that transmitted EMG records could probably be used as indicators of spawning activity of lake trout in at least some of those places in the field where they cannot normally be located by visual means. 1996 The Fisheries Society of the British Isles
Diving birds can lose significant body heat to cold water, but costs can be reduced if heat from exercising muscles or the heat increment of feeding (HIF) can substitute for thermogenesis. Potential for substitution depends jointly on the rate of heat loss, the rate of heat produced by exercise, and the level of HIF. To explore these interactions, we measured oxygen consumption by lesser scaup ducks (Aythya affinis) diving to depths of 1.2 and 2 m at thermoneutral (23 degrees C) and sub-thermoneutral (18 and 8 degrees C) temperatures. Birds dove while fasted and when feeding on blue mussels (Mytilus edulis). Substitution occurred if HIF or costs of diving above resting metabolic rate (RMR) were lower at 18 or 8 degrees C than at 23 degrees C, indicating reduction in the thermoregulatory part of RMR. For fasted scaup diving to 1.2 m, substitution from exercise heat was not apparent at either 18 or 8 degrees C. At 2 m depth, dive costs above RMR were reduced by 5% at 18 degrees C and by 40% at 8 degrees C, indicating substitution. At 1.2 m depth (with voluntary intake of only 14-17% of maintenance requirements), HIF did not differ between temperatures, indicating no substitution. However, at 2 m (intake 13-25% of maintenance), substitution from HIF was 23% of metabolizable energy intake at 18 degrees C and 22% at 8 degrees C. These results show that even with low HIF due to low intake rates, substitution from HIF can add to substitution from the heat of exercise.
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