Swimming Speed and Swimming Metabolism of Atlantic Cod (Gadus morhua) in Relation to Available Food: A Laboratory Study

1993 ◽  
Vol 50 (12) ◽  
pp. 2542-2551 ◽  
Author(s):  
Björn Björnsson

A laboratory study was performed on how young Atlantic cod (Gadus morhua) regulate their swimming speed according to available food. A circular tank 15 m in diameter was divided into six sectors, each containing two cod ranging in length from 29 to 42 cm. Live fish 5 cm long on average were used as prey. For the first 48 d food intake was changed every 1 or 2 wk equally for all six groups. During the last 31 d each group received different amounts of food. The mean swimming speed was highest (0.6 bl/s) when food intake was about half the maximum intake and lowest (0.2 bl/s) when food was unlimited or not available. Swimming metabolism was related to food intake in a similar way, but with a larger difference between the most active (50 mg O2∙kg−1∙h−1) and the least active group (10 mg O2∙kg−1∙h−1). Maximum sustained swimming metabolism was estimated to be about 0.6 times the standard metabolism. The estimated energetic cost of swimming as a percentage of energy obtained from the food decreased with food intake from 24% at maintenance ration to 2% at maximum food intake. On a log–log plot swimming speed decreased linearly with time after encounter of prey.


1989 ◽  
Vol 67 (7) ◽  
pp. 1793-1800 ◽  
Author(s):  
S. L. Poynton ◽  
J. Lom

Trichodina murmanica Polyanskiy, 1955 (= Trichodina domerguei subsp. saintjohnsi Lom and Laird, 1969) and Trichodina cooperi n.sp. were commonly encountered on skin and fins of Atlantic cod, Gadus morhua L., near Halifax, Nova Scotia, Canada. A third species of Trichodina, probably new, was recorded from the skin of one fish. This is believed to be the first report of the genus Trichodina from the body surface of gadoid fish from eastern Canada, and the known geographic range of T. murmanica is extended. Trichodina cooperi n.sp. has an adoral ciliary spiral of 370–380° and is relatively large, the mean diameter of the body is 110 μm, of the adhesive disc (with dark center), 95 μm, and of the denticulate ring, 59 μm. The denticulate ring consists of 24–29 denticles (usually 27), with 7–9 radial pins per denticle. Each denticle has a broad blade, a large central part, and a slightly curved thorn of moderate to broad width, with a central rib when mature. The thorn is approximately twice the length of the blade. The horseshoe-shaped macronucleus has a diameter of 80.0 μm and the micronucleus is in the +y position. Trichodina spp. infected 26% of 39 wild fish 20 to < 60 cm long. Most wild fish yielded less than five ciliates per 24 × 50 mm smear.



1977 ◽  
Vol 34 (12) ◽  
pp. 2411-2413 ◽  
Author(s):  
A. V. Tyler

Juvenile Atlantic cod, Gadus morhua, were forced to swim at speeds of 0.07, 0.6, and 1.2 body lengths/s after eating measured quantities of food. Higher speeds could not be maintained for more than 2 days. Only the highest speed caused a decrease in gastric emptying rate, but the decrease was not of sufficient magnitude to interfere with ration estimates based on digestion rate data. Key words: feeding, swimming speed, digestion rate



2000 ◽  
Vol 203 (3) ◽  
pp. 575-583 ◽  
Author(s):  
C. Olsson ◽  
S. Holmgren

The possible inhibitory roles of pituitary adenylate cyclase-activating polypeptide (PACAP), vasoactive intestinal polypeptide (VIP) and nitric oxide in the control of intestinal motility were investigated in the Atlantic cod, Gadus morhua. Circular and longitudinal smooth muscle preparations developed spontaneous contractions that were inhibited by atropine (10(−)(5)mol l(−)(1)). PACAP 27 and PACAP 38 (10(−)(7)mol l(−)(1)) reduced the amplitude of the contractions but did not usually affect the resting tension. In the circular preparations, the mean active force developed (above resting level; +/− s.e.m.) was reduced from 0. 62+/−0.18 mN to 0.03+/−0.03 mN (N=10) by PACAP 27 and from 0.53+/−0. 20 mN to 0.31+/−0.13 mN (N=7) by PACAP 38, while neither cod nor mammalian VIP (10(−)(10)-10(−)(6)mol l(−)(1)) had any effect. In the longitudinal preparations, PACAP 27 reduced the force developed from 1.58+/−0.22 mN to 0.44+/−0.25 mN (N=8) and PACAP 38 reduced it from 1.61+/−0.47 mN to 0.75+/−0.28 mN (N=5). The nitric oxide donor sodium nitroprusside (NaNP) almost abolished the contractions in the circular preparations, reducing the mean force developed from 0. 47+/−0.05 mN to 0.02+/−0.06 mN (10(−)(6)mol l(−)(1); N=9) and 0+/−0. 07 mN (10(−)(5)mol l(−)(1); N=8). In the longitudinal preparations, NaNP reduced the force developed from 2.03+/−0.36 mN to 0.33+/−0.22 mN (10(−)(6)mol l(−)(1); N=8) and 0.19+/−0.30 mN (10(−)(5)mol l(−)(1); N=8). The L-arginine analogue N(G)-nitro-L-arginine methyl ester (L-NAME; 3×10(−)(4)mol l(−)(1)) enhanced the contractions in both circular and longitudinal preparations, increasing the mean force developed from 0.51+/−0.12 mN to 0.94+/−0.21 mN (N=8) and from 1.49+/−0.36 mN to 3.34+/−0.67 mN (N=7), respectively. However, preincubation with L-NAME before a second addition of PACAP 27 (10(−)(7)mol l(−)(1)) did not affect the response to PACAP, neither did preincubation with the guanylate cyclase inhibitor 6-anilinoquinoline-5,8-quinone (LY83583; 10(−)(5)mol l(−)(1)), while the inhibitory response to NaNP (3×10(−)(7)mol l(−)(1)) was abolished by LY83583. The PACAP analogue PACAP 6–27 (3×10(−)(7)mol l(−)(1)) had no effect on the response to either NaNP (3×10(−)(7)mol l(−)(1)) or PACAP 27 (10(−)(8)mol l(−)(1)) in the circular preparations. These findings indicate the presence of both a cholinergic and a nitrergic tonus in the smooth muscle preparations of the cod. Although PACAP and NaNP both inhibit contractions, there is no evidence of any interactions between the two substances. In addition, NaNP, but not PACAP, probably acts via stimulating the production of cyclic GMP. In conclusion, both PACAP and nitric oxide may act as inhibitory transmitters, using distinct signalling pathways, in the control of intestinal motility in the Atlantic cod.



2004 ◽  
Vol 61 (6) ◽  
pp. 983-991 ◽  
Author(s):  
Björn Björnsson ◽  
Maria Álvaro Dongala Dombaxe

Abstract Nephrops was found to be of low quality as food for cod. In a laboratory experiment the mean specific growth rate of 1 kg cod was 0.184 and 0.415% d−1 when fed to satiation on Nephrops and capelin, respectively. This large difference in growth rate resulted not only from less intake of Nephrops (1.19 kg cod−1) than capelin (1.55 kg cod−1) but also because more Nephrops (4.6 kg) than capelin (2.2 kg) were required to produce each kilogramme of cod. Higher food conversion ratio was consistent with lower fat content of Nephrops (1.3%) than capelin (9.2%) but the exoskeleton also reduced the digestion rate of Nephrops. In the groups where Nephrops and capelin of equal mean weight were offered simultaneously, 40% of the diet consisted of Nephrops during the first week and 10% during the final seven weeks of the experiment. At the end of the experiment, condition factor, liver index, and gonadosomatic index were significantly lower for cod fed on Nephrops (0.967, 5.7, 7.1, respectively) than for those fed on capelin (1.086, 15.8, 11.2, respectively). These results suggests that predation by cod on Nephrops might be reduced by regular release of capelin or other similar food in the distributional areas of Nephrops.



2000 ◽  
Vol 57 (6) ◽  
pp. 1200-1207 ◽  
Author(s):  
Paul D Winger ◽  
Pingguo He ◽  
Stephen J Walsh

The swimming endurance of Atlantic cod (Gadus morhua), native to the cold waters off the east coast of Newfoundland and Labrador, was investigated under laboratory conditions. Using a swimming flume, endurance was tested at swimming speeds ranging from 0.6 to 1.3 m·s-1 using water temperatures from 0.0 to 9.8°C ( mean = 3.2°C, SD = 2.8) and fish lengths from 41.0 to 86.0 cm ( mean = 57.8 cm, SD = 10.5). The results revealed that swimming speed was the only significant factor affecting the endurance of cod. The maximum sustained swimming speed (Ums) was predicted to be 0.66 m·s-1. Statistical analysis of the data was conducted using failure time analysis. The hazard, or risk of exhaustion, was found to increase rapidly with increasing swimming speed, i.e., there was a decrease in the probability of cod achieving a given swimming endurance. Probability curves for the endurance of cod were calculated for different swimming speeds. The findings suggest that the catching efficiency of commercially targeted cod (>41.0 cm) by otter trawls may be highly sensitive to changes in towing speed while being independent of both fish length and water temperature.



1994 ◽  
Vol 51 (7) ◽  
pp. 1569-1576 ◽  
Author(s):  
Yvan Lambert ◽  
Jean-Denis Dutil ◽  
Jean Munro

Growth rates of Atlantic cod (Gadus morhua) were measured under different salinity conditions to test the hypothesis that growth would be best in an isosmotic environment. The results of two experiments (spring and autumn 1991) conducted at three different salinities (7, 14, and 28‰) and two feeding regimes indicate a significant effect of salinity and ration on growth rate. Within each experiment, growth rates were highest for cod maintained in intermediate salinity conditions (14‰). Growth rates in low salinity conditions (7‰) were higher than in seawater (28‰) during the spring, but during the autumn, growth rates of cod held under low salinity conditions and in seawater were similar. Higher growth rates at lower salinities resulted from an increase in food conversion efficiency. They were not associated with an increase in food intake, changes in composition (proteins, lipids, or water), or relative allocation of energy to the tissues (muscle, liver, and gonads) of cod. The results indicate that rearing cod at intermediate salinities, such as would occur in estuaries or coastal regions, could confer an advantage for cod aquaculture.



1997 ◽  
Vol 54 (3) ◽  
pp. 670-685 ◽  
Author(s):  
P Pepin ◽  
J A Helbig

We present the results of a study designed to ascertain the importance of variations in transport of cod eggs and larvae on the northeast Newfoundland Shelf. The distribution of cod eggs and larvae is described from a series of ichthyoplankton surveys. The mean and variance in surface currents were estimated from five experiments in which clusters of drogued satellite-tracked drifters were released at the presumed northern limit of the stock's range. These data were used to project the patterns of drift both backward and forward in time and thus the possible sources and destinations of eggs and larvae. Considering the development from the youngest (stage I) to the oldest stages (larvae), we saw a north-to-south and an offshore-to-inshore progression in spatial patterns of spawning and a continuing increase in the overall level of dispersion with increasing age of offspring. The data do not support the hypothesis that coastal or offshore areas represent simple sources or sinks of cod eggs and larvae. Transport plays an important but highly variable role that is coupled to the spawning distribution of adult fish and the availability of suitable conditions or habitats when the young begin to undergo metamorphosis and settle.





2009 ◽  
Vol 66 (7) ◽  
pp. 1095-1106 ◽  
Author(s):  
Matthew J. Gollock ◽  
Kristopher J. Hunter ◽  
Douglas A. Syme ◽  
Marcus Freeman ◽  
R. Scott McKinley ◽  
...  

As there are no commercially available acoustic telemetry devices for quantifying the swimming activity and activity-related metabolic expenditures of a wide range of marine species, we (i) examined the suitability of three methods (electromyography; sonomicrometry; and tail differential pressure tags (DPT)) for measuring the swimming speed of Atlantic cod ( Gadus morhua ), and indirectly, metabolic rate (MO2) and (ii) measured the activity pattern of free-swimming cod carrying the DPT. All three methods yielded significant relationships with swim speed during a critical swimming speed (Ucrit) test. However, only the DPT was able to discern between swimming speed differences of 0.1 body lengths (BL)·s–1 and provide a strong relationship with MO2. Further, we found that free-swimming cod fitted with the DPT swam at an average speed of 0.33 BL·s–1, the speed previously reported to result in minimal cost of transport for this species. While the DPT has considerable potential for assessing the bioenergetics of marine fishes, the swimming economy of tagged Atlantic cod was lower above 0.4 BL·s–1 as compared with untagged fish, and Ucrit was reduced by 25%. These latter effects are likely related to the tag’s present size (39 g) and design.



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