Effects of feeding and starvation on growth and swimming activity in an obligatory air-breathing fish

Reared in (tubular) aquaria containing different depths of water, Ophiocephalus striatus (0.7 g, 4.5 cm body length), an obligatory air-breathing tropical fish, swam long or short distances to enable themselves to exchange atmospheric air. In each tested depth (2.5, 5.0, 15.5, 31.0 and 40.0 cm) series, one group was starved, while the other was fed ad libitum twice a day on fish muscle. In the shallowest water (2.5 cm depth), the feeding group surfaced 1,294 times, travelling 64.7 m at an energy cost of 20.4 mg dry fish substance/g live fish/day, against those exposed to the deepest water (40 cm depth), which expended 35.8 mg/g/day, swimming 1,503.4 m on 1,879 visits to the surface. The starving group surfaced only 482 times, travelling 24.1 m at an expense of 5.8 mg/g/day in the shallowest water, while those at 40 cm depth surfaced 504 times, swimming 403.2 m at an energy cost of 7.4 mg/g/day. Owing to the sustained swimming activity and the consequent fatigue, the test individuals belonging to both groups in all the tested series hang to the surface for a definite interval, repaying the O₂ debt. Observations were also made to assess the duration of hanging to precisely estimate the distance travelled. Irrespective of changes in depths of water, the duration of hanging to surface was only 3.0 hr/day for the feeding groups, while it was as much as 15.5 hr/day for the starving groups. The maximum sustained metabolic level of O.striatus reared in 40 cm depth was equivalent to 1.23 ml O₂/g/hr, which is about 2 times higher than the value reported for the active metabolism of swimming Oncorhynchus nerka at 15°C in Brett's (1964) respirometer. O.striatus reared in 2.5 cm depth fed 32.0 mg and converted 6.7 mg dry food/g live fish/day, while those exposed to the deepest water fed 49.1 mg, but converted only 5.5 mg/g/day. Culturing obligatory air-breathing fishes in shallow waters will be advantageous.     

Circadian rhythms in juvenile american shad, Alosa sapidissima

Swimming activity (in cm s⁻¹) of a school (55 individuals) of young-of-the-year ( total length=110 mm) American shad, Alosa sapidissima , was determined under a variety of photoperiod conditions. These included a normal (ambient), a shifted, and constant-light day. Swimming activity was measured over 4-day periods. During normal days swimming speeds followed periods of about 24 h, with fast speeds (up to 45 cm s⁻¹) and schooling occurring during the photoperiod. Under dark conditions speeds were slower (8 cm s⁻¹) with most fish swimming as individuals. During a shifted day swimming speeds and schooling corresponded to the imposed day. Under constant light (equivalent to bright moonlight) no schooling was evident, and a constant, but slow, swimming speed was observed in each 24-h period. These shad demonstrated an exogenous rhythm with respect to the imposed day length. It is hypothesized that an endogenous circadian rhythm would only be of use to a fish required to hunt or chase its prey. Shad, being plankton feeders, do not chase prey and therefore can exhibit an exogenous circadian rhythm with no detrimental feeding results.     

Food intake,conversion and swimming activity in the air-breathing catfish Heteropneustes fossilis

Summary Reared in tubular aquaria containing 20, 40 and 60 cm depth 0f water, Heteropneustes fossilis (20 g; 17 cm body length), an air-breathing catfish, swam 40, 80 and 120 cm/surfacing to exchange atmospheric air. With decreasing Po₂, the starving groups reduced the surfacing, whereas, the decrease in the Po₂ beyond 70 mm Hg induced the feeding groups to surface more frequently. Feeding groups exposed to 20 and 40 cm depth surfaced 353 and 423 times, travelling distances of 141 and 338 m/day, at the energy cost of 8.5 and 9.7 mg dry fish substance/g live fish/day, respectively. The corresponding starving groups surfaced only 163 times/ day and swam 65 and 130 m/day at the expense of 1.2 and 1.6 mg/g/day. Feeding and starving groups reduced the number of surfacing, when the distance they have to swim exceeded 0.8 m/day and increased the proportion of O₂ taken up branchially; the starving and feeding groups exposed to 60 cm depth surfaced only 70 and 271 times, swimming 84 and 325 m/day, at the energy cost of 2.9 and 17.6 mg/g/day. Feeding and conversion rates steadily increased from 16.9 mg dry liver/g live fish/day and 6.7 mg dry fish substance/g live fish/day in those exposed to the shallowest aquarium to 27.4 mg/g/day and 7.0 mg/g/day in those exposed t0 the maximum depth, respectively; conversion efficiency was 44% in the former and 28% in the latter; hence culturing H. fossilis in the shallow waters is profitable.     

Comparative swimming abilities of fed and starved larval largemouth bass (Micropterus salmoides)†

Sustained swimming abilities of fed and starved larval largemouth bass (Micropterus salmoides L.) were compared in the first week after swimming initiation. Fed larvae improved to a sustained velocity of 4·0 cm/sec while starved larvae attained a velocity of only 1·5 cm/sec. Swimming behaviour for fed and starved larvae was quantified for number of moves, average distance/move, and total distance for all moves in 1 min intervals. Fed larvae were always more active than starved larvae, although real differences did not appear until the 4th day after swimming initiation.     

Surfacing activity and food utilization in a tropical air-breathing fish exposed to different temperatures

Reared in tubular aquaria containing different depths of water (2.5, 5.0, 15.5, 31.0 and 40.0 cm), the obligatory air-breathing fish Ophiocephalus striatus (760 mg; 4.5 cm L) was forced to swim vertically a longer or shorter distance per surfacing. Interaction of temperature (17, 22, 27, 32 and 37°C) and aquarium depth reveals that surfacing frequency of the fish, fed ad libitum on Tilapia muscle, increased with increasing aquarium depth, but the increase was significant only at 27 and 32°C; in the starving series, the frequency was not depth-dependent at any temperature. Owing to the sustained surfacing activity and the consequent fatigue, the test individuals ‘hung’ to the surface for a definite period. Hanging frequency was temperature-dependent, but not a depth-dependent activity either in the starving or feeding series. At any temperature and aquarium depth, the feeding series hung more frequently than the starving series. Hanging duration increased from about 1 hr/day in either series at 17°C to 6 and 18 hr/day in the feeding and starving series at 37°C. At any tested temperature, distance swum by the feeding and starving series was a depth-dependent activity. The feeding series at 32°C exhibited the maximum swimming speed of 2 L/sec for 4.8 hr/day in the 40 cm depth. With increasing temperature and depth, feeding rate increased (from 24 to 225 g cal/g live fish/day); between 17 and 27°C, it was more a temperature-dependent activity. The highest rate (47 g cal / g/day) and efficiency (27%) of conversion were observed at 32°C; whereas the efficiency was depth-dependent, the rate was not. Oxygen uptake was a temperature-dependent activity; aquarium depth played a secondary role. Briefly, O. striatus in deeper aquaria consumed significantly more food and converted lesser, as it surfaced more frequently and swam longer distance, dissipating more energy on metabolism and swimming activity. Hence, culturing O. striatus in shallow waters at the optimum temperature of 32°C will be advantageous. This work was supported by the University Grants Commission's (New Delhi) grant to Dr. T. J. Pandian: Grant No. F. 23-210/75 (Sr II) for which appreciation is expressed.     

Estimation of fish activity costs using underwater video cameras

Swimming speed and activity costs of dace ( Phoxinus eos × P. neogaeus ) were estimated in the field using underwater video cameras. Activity costs were estimated by converting swimming speeds and the number of movements into swimming costs. Average swimming speed ranged from 6.7 to 12.2 cm.s⁻¹ across 2 h periods and varied significantly among dates and time of day. The time spent swimming by dace ranged from 616 to 17 640 s 2 h⁻¹. Activity costs per 2h period ranged from 2.1 to 4O.2J 2h⁻¹ and were strongly correlated to the time spent swimming. Daily activity cost estimated using the cameras averaged 128.9J day⁻¹ and was equivalent to 1.7 times the standard metabolic rate. Activity cost predicted using a bioenergetic model in conjunction with independent estimates of consumption and growth rates averaged 138.8J day⁻¹. This study indicated that swimming characteristics and activity costs of dace varied significantly both within and among days. These analyses also indicated that equally valid activity costs for fish in the field can be estimated using video cameras and the difference between Consumption and growth rates.     

不同体质量和饥饿程度对红鳍东方鲀幼鱼游泳能力的影响

为了考察不同体质量和饥饿程度红鳍东方鲀(Takifugu rubripes)幼鱼的游泳能力,利用行为生态学方法测定了不同体质量(0.22—3.31 g)和饥饿天数(1d、3d、6d和9d)下红鳍东方鲀幼鱼的绝对临界游速(U_crit,cm/s)、相对临界游速(U_crit’,体长/s,BL/s)、偏好游速(U_pref,cm/s)、6个流速区域(2—36 cm/s)下停留时间百分比(P_t,%)、偏好区域平均流速(V_mean,cm/s)和总游泳距离(D_1h,m)等游泳行为指标。结果显示,体质量和饥饿显著影响红鳍东方鲀幼鱼的U_crit、U_crit’、P_t、V_mean和D_1h。随体质量增加,实验鱼的U_crit、U_pref、V_mean和D_1h均逐渐升高,而U_crit...     

A study of the swimming performance of the Crucian carp Carassius carassius (L.) in relation to the effects of exercise and recovery on biochemical changes in the myotomal muscles and liver

A study has been made of the maximum sustained swimming speed of Crucian carp Carassius carassius (L.) using a fixed velocity technique. The data obtained from swimming tests on 214 carp have been analysed using the method of probit analysis. The 50% fatigue level for 13–16 cm fish acclimated to 9.5±0.6°C has been estimated to be 3.35 lengths/sec. Biochemical measurements have been made on the red and white myotomal muscles and liver of fish subjected to both varying intensities of sustained swimming and short periods of vigorous swimming. Free creatine was found to increase only during high speed swimming in the white muscle. Elevated lactate concentrations occurred at both low and high sustained swimming speeds in the red superficial muscle but not during short periods of strenuous exercise. Glycogen depletion from the red musculature also only took place at the sustained swimming speeds investigated. The reverse situation was operative in the white muscle, significant glycogen depletion occurring only at the highest swimming speed studied. Lactate levels were only significantly different from non-exercised fish in the fish swimming at the higher velocities. The effects of periods of recovery following 200 min of sustained swimming were also investigated. White muscle lactate was at a higher level than non-exercise fish 5 h post-exercise, while both red muscle glycogen and lactate rapidly returned to pre-exercise concentrations. Biochemical measurements on the myotomal muscle types have been discussed in relation to the swimming performance of the fish and the division of labour between red and white fibres.     

Schwimmverhalten und Schwimmgeschwindigkeit bei den Larven des HeringsClupea harengus

The present study is based on two year experiments; it analyses swimming behaviour and swimming speed at different developmental stages of the herring. Yolk sac larvae tend to sink rather rapidly during resting phases. At the end of the yolk sac stage the sinking rate is at its minimum; it increases again with increasing larva size. During the phase of yolk sac resorption, vertical movements become gradually transformed into horizontal ones. Generally, three types of swimming can be distinguished: (1) “Abrupt swimming” consisting of very short periods of fast swimming; normally each dart is connected with a change in swimming direction. (2) “Normal swimming” characterized by steady movements for several seconds; it results in a winding path. (3) “Slow meandering” representing search swimming, a slowly winding locomotion with a large amplitude of each winding but with very little net progression of the larva. Swimming speed varies considerably in all size groups. The 8 to 11 mm (total length) larvae reach a mean swimming velocity (undulation) of 1.0 to 1.2 cm per second. Swimming speed, measured as the straight line distance between start and end points of a single swimming phase, attains mean values of 7 to 8 mm/sec in 8 to 11 mm larvae, 10 to 11 mm/sec in 11 to 15 mm larvae, 21 to 25 mm/sec in 19 to 24 mm larvae, and 40 to 50 mm/sec in 32 to 40 mm larvae. Swimming activity changes during larval development and seems to be influenced by food supply. The total distance travelled in 5 minutes by the head of a yolk sac larva is 1 to 3 m. About 8 days after hatching, sinking rate is low and “search swimming” (slow meandering movements) prevails. The path covered by the head within 5 minutes is 0.8 to 1.5 m.     

流速对红鳍银鲫幼鱼游泳状态的影响

在28℃水温下,采用特制的鱼类游泳行为测定装置,研究体重(125.94±13.87)g的红鳍银鲫(Barbodes schwanenfeldi)幼鱼在0.0m/s(对照组)和0.1m/s、0.3m/s、0.5m/s3种流速下的游泳行为。结果表明,从0.0～0.3m/s,红鳍银鲫幼鱼平均趋流率和摆尾频率均随着流速的增加而增大,而0.5m/s组在90min内随时间延长而下降。红鳍银鲫游泳状态明显受到所处流速的影响,在静水对照组以"逆流前进"和"顺流而下"为主,两者共占总观察时间的98%以上;各流速组均以逆流静止为主,且随着流速的增大,逆流静止所占时间比例从45.8%增加至81.3%,而逆流前进所占时间比例由24.1%减至5%以下;逆流后退所占时间比例以0.1m/s组最大,为16.4%;顺流而下的比例随着流速增大先减小后增大,3个流速组依次为13.7%、2.1%和10.9%。红鳍银鲫幼鱼的游泳速度(V)和摆尾频率(TBF)在逆流前进及逆流静止两种游泳状态下呈线性正相关,而在逆流后退和顺流而下两种状态下两者没有显著相关。     

Swimming activity of seabass: comparing patterns obtained in natural environment and in re-circulating tanks under high density

Seabass ( Dicentrarchus labrax ) swimming activity was compared between natural environments and aquaculture facilities. Behaviour under natural conditions was assessed in a saltmarsh pond (250 m², 18 × 14 × 0·8 m) using acoustic telemetry. From several surveys, we documented the diel activity rhythm and demonstrated group effects on swimming patterns and amplitudes by comparing activity of solitary fish with that of a fish living in a group of 60. Consequences of weather variability were also analysed and revealed a high sensitivity of fish to atmospheric conditions for both swimming and demand‐feeding behaviour. Behaviour in fish tanks was also studied using acoustic telemetry, as part of the EUREKA EU1 960 'Aqua‐Maki 2' project investigating aspects of fish culture in re-circulating tanks under high density. A re-circulating hexagonal tank (5·4 × 5·4 m, 1·8 m depth, 48 m³) was equipped with positioning and demand‐feeding systems, oxygen and temperature probes. Initial density was 50 kg m³ in March and rose to 90 kg m³ at the end of the experiment in May. During this period, the movements of nine fish were continuously recorded for 24 h each, reaching a total of six 24 h episode at eight days interval. Swimming activity was analysed in terms of activity rhythms and space occupation specially around feeding events. The two data set and main results will be presented and compared to assess seabass behavioural plasticity and sensitivity to husbandry conditions.     

Activity and properties of phosphofructokinase from while muscle of the horse mackerel Trachurus mediterraneus during simulation due to swimming

The activity and properties of phosphofructokinase (PFK) in tissues of horse mackerel which was swimming at burst regimen for 5 min and at cruiser one for 60 min have been investigated. In white muscle the PFK activity increased 1.6-fold after burst swimming and Hill's coefficient rose as well and decreased 3-fold after cruiser one. Swimming did not change the half-maximal saturation constant for both substrates and inhibition constants for ATP and citrate. In the preparations from white muscle of fish which were stimulated by burst swimming the PFK activity at physiological pH values (6.0-7.0) was higher comparing with one from the control group and after cruiser swimming. Incubation of preparations at 45 degrees C decreased the activity of PFK in control and cruiser swimming groups (to 61-67% of initial level) and increased it after burst swimming (1.3-fold). The mechanisms involving in stable modification of PFK under different swimming regimens are discussed.     

The swimming endurance of threespine sticklebacks, Gasterosteus aculeatus L., from the Afon Rheidol, Wales

The endurance of threespine sticklebacks, Gasterosteus aculeatus , swimming with pectoral fin locomotion at 20° C in a laboratory flume was measured. Each trial lasted a maximum of 480 min. At a speed of 4 body lengths per sec (L s⁻¹) all fish were still swimming at the end of the trial, but endurance decreased at higher speeds. At speeds of 5 or 6 L s⁻¹ (20–30 cm s⁻¹) a few fish still maintained labriform locomotion for the 480 min. However, at a speed of 7 L s⁻¹ all fish furled their pectoral fins and used body and caudal fin propulsion but fatigued rapidly. During sustained swimming, fish could cover distances of 6 km or more. No significant differences between males and females were found.     

Induced swimming modified the antioxidant status of gilthead seabream (Sparus aurata)

Swimming has relevant physiological changes in farmed fish, although the potential link between swimming and oxidative stress remains poorly studied. We investigated the effects of different medium-term moderate swimming conditions for 6 h on the antioxidant status of gilthead seabream (Sparus aurata), analyzing the activity of enzymes related to oxidative stress in the liver and skeletal red and white muscle. Forty fish were induced to swim individually with the following conditions: steady low (SL, 0.8 body length (BL)·s⁻¹), steady high (SH, 2.3 BL·s⁻¹), oscillating low (OL, 0.2–0.8 BL·s⁻¹) and oscillating high (OH, 0.8–2.3 BL·s⁻¹) velocities, and a non-exercised group with minimal water flow (MF, < 0.1 BL·s⁻¹). All swimming conditions resulted in lower activities of superoxide dismutase (SOD), glutathione reductase (GR), and glutathione-S-transferase (GST) in the liver compared to the MF group, while steady swimming (SL and SH) led to higher reduced glutathione/oxidized glutathione ratio (GSH/GSSG) compared to the MF condition. Swimming also differently modulated the antioxidant enzyme activities in red and white muscles. The OH condition increased lipid peroxidation (LPO), catalase (CAT) and glutathione peroxidase (GPx) activities in the red muscle, decreasing the GSH/GSSG ratio, whereas the SL condition led to increased GSH. Oscillating swimming conditions (OL and OH) led to lower CAT activity in the white muscle, although GPx activity was increased. The GSH/GSSG ratio in white muscle was increased in all swimming conditions. Liver and skeletal muscle antioxidant status was modulated by exercise, highlighting the importance of adequate swimming conditions to minimize oxidative stress in gilthead seabream.     

Daily ration of juvenile Coregonus lavaretus (L.) fed on living zooplankton

Juvenile whitefish, Coregonus lavaretus (L.), wet weight 0.04 to 5.2 g, from Lake Constance were kept at 10, 12 and 16° C water temperature, respectively and fed with living zooplankton. The experimental duration lasted 72 to 120 h. Daily rations were defined as the amount of zooplankton remaining subtracted from the amount of zooplankton added after a 24 h interval. The mortality of the zooplankton was determined in parallel experiments without fish. Relative daily ration (zooplankton weight/fish weight) v. fish weight increased up to a fish dry weight of approximately 0.12 g and then decreased steadily. The maximum daily ration was about 270% of fish body wet weight (wet/wet) corresponding to 75% of body dry weight (dry/dry), respectively. In fishes of a dry weight higher than 0.12 g (wet weight 0.65 g) a significant difference in food intake was found between 12 and 16° C. The specific growth rate ranged from nearly 0 up to 33% per day. No correlation was found between daily ration and specific growth rate.     

Locomotion of bluefish.

1. Pressure previously measured on the body surface of swimming bluefish were resolved into their backward vectorial components to allow calculation of profile drag. It was 0.18 kg at a speed of 1.8 m/sec. Tangential drag was calculated as if for a thin plate of an area equal to that of the fish. It was 0.08 kg at 1.8 m/sec. Net drag, 0.26 kg, was the sum of profile and tangential drag. 2. Thrust and drag also were calculated from the changes of acceleration measured during steady swimming, assuming that thrust took place only during the acceleration phase, whereas drag occurred during both acceleration and deceleration. This drag was 0.08 kg at a speed of 1.1 m/sec. It is compatible with the drag of 0.26 at 1.8 m/sec calculated from profile and tangential drag provided drag varies as the square of velocity. 3. The force required to produced maximal acceleration was measured during a scare. It was calculated to be 6.9 kg at a peak acceleration of 3 g. 4. The compression strength of th vertebrae was found to be approximately 20 kg per cm2, or roughly three times the force encountered during maximal acceleration. This safety factor of 3 would be reduced when the back was curved, or if opposing groups of muscles were under tension. 5. The finding that a bluefish can accelerate at 3 g and that the vertebral column is strongg enough to withstand this force indicates that the muscles and body structure of a bluefish would be able to withstand the force of gravity if the fish were otherwise equipped for terrestrial life. This fish may have evolved these strengths simultaneously with land animals. It is speculated that other fish may have evolved some degree of strength to overcome inertia and drag during aquatic locomotion, and this evolution may have been a prelude to terrestrial locomotion.     

Swimming performance of European eel (Anguilla anguilla (L.)) elvers

To determine the relation between swimming endurance time and burst swimming speed, elvers of the European eel, Anguilla anguilla (L.), were made to swim at speeds from 3.6 to 7.2 L (body lengths) s⁻¹ in both fresh and sea water. Swimming endurance time of elvers averaging 7.2 cm total length decreased logarithmically with increased swimming speed from 3.0 min at 3.5 L s⁻¹ to 0.7 min at 5.0 L s⁻¹, and again logarithmically but with a lesser slope to 0.27 min at 7.5 L s⁻¹. No differences were found between fresh and sea water elvers. In still water, elvers could swim at high speeds for about 10–45m before exhaustion, depending upon speed. Elvers would be able to make virtually no progress against water currents >50 cm s⁻¹. Drift in coastal water currents and selective tidal transport probably involve swimming speeds below those tested in this study. Migration into freshwater streams undoubtedly involves avoidance of free stream speeds and a combination of burst and sustained swimming.     

Endurance swimming of diploid and triploid Atlantic salmon

When groups of diploid (mean ±  s . e . fork length, L _F) 33·0 ± 1·4 cm and triploid (35·3 ± 0·5 cm) Atlantic salmon Salmo salar were forced to swim at controlled speeds in a carefully monitored 10 m diameter 'annular' tank no significant difference was found between the maximum sustained swimming speeds ( U _ms, maintainable for 200 min) where the fish swam at the limit of their aerobic capability. Diploids achieved 2·99 body lengths per second (bl s⁻¹)(0·96 m s⁻¹) and triploids sustained 2·91 bl s⁻¹(1·02 m s⁻¹). The selection of fish for the trials was based on their ability to swim with a moving pattern projected from a gantry rotating at the radius of the tank and the selection procedure did not prove to be significant by ploidy. A significant difference was found between the anaerobic capabilities of the fish measured as endurance times at their prolonged swimming speeds. During the course of the experimentation the voluntary swimming speed selected by the fish increased and the schooling behaviour improved. The effect of the curvature of the tank on the fish speeds was calculated (removing the curved effect of the tank increased the speed in either ploidy by 5·5%). Implications of the endurance times and speeds are discussed with reference to the aquaculture of triploid Atlantic salmon.     

Ventilation and metabolic rate of young rainbow trout (Salmo gairdneri) exposed to sublethal environmental pH.

Differences between ventilatory response and metabolic rates of young rainbow trout tested within the sublethal range of pH 6 to pH 9 were observed using a flowing water respirometer. The oxygen consumption was monitored at swimming speeds of 12 cm/sec and 24 cm/sec. The oxygen consumption rates at 24 cm/sec and pH 6 (423 mg/kg-hr) and pH 9 (367 mg/kg-hr) were considerably higher than those determined near neutrality (328 mg/kg-hr). Ventilation rate increased to either side of neutrality, but significantly fewer respiratory reversals, or "coughs," were observed at pH 6 and a greater number at pH 9 than occurred at pH 7 and 8 or in untested fish. The respiratory-cough response is shown to be pH-dependent in rainbow trout and may therefore not be as reliable an indication of pollutant-caused stress in studies where the experimental pH has not been specified or controlled.     

Surfacing activity and food utilisation in the obligatory air-breathing fish ophiocephalus striatus as a function of body weight

Reared in cylindrical aquaria containing different depths of water (2.5 to 70 cm) the obligatory air-breathing fish Ophiocephalus striatus, belonging to different weight classes (0.1, 0.75, 10, 20 and 41 g), was forced to swim vertically a longer or shorter distance per surfacing. Surfacing frequency was a depth-dependent, activity in individuals weighing less than 20 g in all weight classes, the frequency was nearly 2 times more in the series fed ad libitum on fish muscle, than in the one where the fish were starved. Owing to the sustained surfacing activity and the consequent fatigue, the test individuals hung to the surface for a definite period. Neither frequency nor duration of hanging was depth-dependent. Mean hanging durations for the feeding series were 1.1, 3.8, 5.9, 7.9 and 8.8 hr/day in the 0.1, 0.75, 10, 20 and 41 g weight classes, respectively; the corresponding values for the starving series were 1.3, 15.0, 13.0, 12.7 and 12.8 hr/day. The distance swum by the feeding fish increased from 57 to 681 m/day and from 61 to 507 m/day in the 0.1 and 41 g individuals exposed to the minimum and maximum aquarium depths. Feeding rate, which was a depth-dependent activity, decreased from 280 to 113 g cal/g live fish/day with increasing weight. Rate and efficiency of conversion also decreased with increasing body weight; in larger fish conversion was dependent on volume rather than on depth of the aquarium. O₂ uptake of feeding fish was about 6 times higher than the starving ones of the tested weight classes at different aquarium depths.This paper is part of a thesis submitted by the author (from A.P.A. College, PALNI) to Madurai University in partial fulfillment of the requirement of the Ph. D. degree. Contribution No. 12 under a research scheme granted to Dr. T. J. Pandian by the UGC (New Delhi). The author is grateful to Dr. T. J. Pandian for valuable guidance, financial support and encouragements.