Djungarian hamsters ( Phodopus sungorus) acclimated to a short photoperiod (8:16-h light-dark cycle) display spontaneous daily torpor with ad libitum food availability. The time course of body temperature (Tb), metabolic rate, respiratory quotient (RQ), and substrate and enzyme changes was measured during entrance into torpor and in deep torpor. RQ, blood glucose, and serum lipids are high during the first hours of torpor but then gradually decline, suggesting that glucose is the primary fuel during the first hours of torpor, with a gradual change to lipid utilization. No major changes in enzyme activities were observed during torpor except for inactivation of the pyruvate dehydrogenase (PDH) complex in liver, brown adipose tissue, and heart muscle. PDH inactivation closely correlates with the reduction of total metabolic rate, whereas in brain, kidney, diaphragm, and skeletal muscle, PDH activity was maintained at the initial level. These findings suggest inhibition of carbohydrate oxidation in heart, brown adipose tissue, and liver during entrance into daily torpor.

Bulldog fish (Marcusenius macrolepidotus) generate short (<1 ms) electric-organ discharges (EODs), separated by much longer and highly variable interdischarge intervals (IDIs). We observed overt behaviour and electrical activity during reproductive behaviour in a male and in a female bulldog, and identified IDI patterns with putative signal functions. In contrast to Pollimyrus adspersus and Pollimyrus isidori, in which an elaborate and extended courtship precedes spawning proper, our fish started spawning almost immediately when we allowed the female to enter the male's territory. The male did not construct a nest, and neither parent provided parental care. The male showed very little aggression towards the intruding female. Fish spawned in bouts near the male's hiding place, and eggs were scattered by the female's vigorous tail flips as she left the spawning site, only to return shortly thereafter. During spawning bouts, both fish generated highly stereotyped IDI patterns: the male generated a series of IDIs gradually decreasing from about 200 ms to about 55 ms that was abruptly terminated by a long IDI. The female generated a series of relatively regular IDIs (about 54 ms) that was followed by a marked increase in IDI duration (the probable time of spawning). Finally, a sharp decrease in IDIs to about 20 ms accompanied the female's sudden escape from the spawning site. In between spawning bouts, both fish generated series of very short IDIs (high discharge rate, HD) that alternated abruptly with very low-rate inter-HD activity (especially in the male). IDIs as short as 9 ms (male) or 11 ms (female) occurred during HD displays. No visible aggression, in fact very little overt behaviour, occurred during these HD displays in both fish. Agonistic interactions between male and female, outside a reproductive context, were similar to those previously described in male pairs, including overt behavioural patterns such as parallel swimming, antiparallel display and attack, as well as HD displays. When not interacting, fish did not generate HD displays. We suggest the HD display is a communication signal in both reproductive and agonistic contexts.

South African bulldogs ( Marcusenius macrolepidotus , Mormyridae) generate brief (less than 1 ms) electric organ discharges (EODs), separated by much longer and highly variable inter-discharge intervals (IDIs). The diurnal and nocturnal overt behaviour and electrical activity were studied under various conditions: in isolated fish, in pairs of fish, and in a group of four fish that were kept in a "natural" large aquarium. EODs from up to four individuals were recorded simultaneously and identified. While resting during the day, isolated fish showed a broad inter-individual variability of IDI patterns, with distribution histogram modes ranging from 85.7 ms to 325.8 ms. When foraging during the day, IDI modes were shorter and less variable (36.3-48.3 ms). Behaviour patterns displayed during nocturnal agonistic encounters were retreating, parallel swimming, anti-parallel display, attack, and fleeing/chasing. High-discharge-rate (HD) displays were observed at several stages of these encounters, for example, during antiparallel display (a period of low overt motor activity), or following attacks. IDI durations as short as 11 ms occurred during HD displays, which followed low-rate inter-HD activity almost without transition. IDI distribution histogram modes when fish showed anti-parallel display were 15.4 ms and 24.8 ms, and 30.0 ms during nocturnal nonagonistic interactions. No overt fighting was observed once a dominance relationship was established. In a large aquarium, an approaching dominant male evoked a simultaneous discharge arrest in a group of three subdominant males.

The emergence and development of the electric-organ discharge (EOD) in larvae and juvenile bulldog Marcusenius macrolepidotus was investigated. Larvae hatched 4-5 days after spawning, and the first EODs were recorded on days 9 and 10 at a standard length (L S ) of c. 6Á5 mm. The larval EOD waveform was virtually monopolar, with a strong head-positive phase followed by a weak head-negative phase of long duration. A small separate potential preceded the EOD by c. 1Á6 ms (believed to represent postsynaptic potential from electrocyte stalks). In contrast to previous reports on Pollimyrus adspersus with its distinct larval and adult EODs, in M. macrolepidotus there was a gradual transformation of the larval into the adult EOD waveform. The transformation started at an L S of c. 17 mm (at an age of c. 40 days), first indications being a decrease in duration of the head-negative phase, and an increase of its peak amplitude relative to that of the head-positive phase. Still later, the weak postpotential of the adult EOD emerged on the rising edge of the head-negative phase. The transformation was nearly completed at an L S of c. 30 mm (at an age of c. 60 days). Evolutionary and behavioural consequences of this alternative path of EOD ontogeny are discussed.