The Growth Rate of Brown Trout (Salmo trutta L.) Fed on Reduced Rations

10.2307/3721 ◽  
1975 ◽  
Vol 44 (3) ◽  
pp. 823 ◽  
Author(s):  
J. M. Elliott
1991 ◽  
Vol 48 (10) ◽  
pp. 1838-1845 ◽  
Author(s):  
Bror Jonsson ◽  
Jan Henning L'Abée-Lund ◽  
Tor G. Heggberget ◽  
Arne J. Jensen ◽  
Bjørn O. Johnsen ◽  
...  

Longevity in 25 populations of anadromous brown trout (Salmo trutta) showed a significant trend with increasing life span at latitudes of 58–70°N in Norway, with the largest change from 58 to 60°N. Moreover, longevity was negatively correlated with temperature and growth rate in freshwater and at sea. Body size was negatively correlated with water temperature and growth rate in freshwater, but not with latitude or water temperature and growth rate at sea. Thus, conditions influencing development and metabolic rates in fresh water seem more important than conditions in the sea in determining variation in longevity and body size of anadromous brown trout. Our results support the hypothesis that interpopulation variation in longevity and body size is influenced by rate of metabolism, chiefly influenced by ambient water temperature.


1974 ◽  
Vol 31 (11) ◽  
pp. 1824-1826 ◽  
Author(s):  
Hugh A. Poston

Growth rate, body composition, and intake of either dry matter or energy did not differ significantly (P > 0.05) between two groups of juvenile brown trout (Salmo trutta) fed either a low- or high-moisture semipurified diet at different rates to compensate for a diet energy density gradient. Feed/gain efficiency, on an as-fed basis, was significantly greater (P < 0.01) in fish fed the low-moisture diet, but did not differ (P > 0.05) when compared on the basis of dry matter or energy intake.


1989 ◽  
Vol 46 (6) ◽  
pp. 1067-1076 ◽  
Author(s):  
Richard J. Preall ◽  
Neil H. Ringler

A ratio of specific growth rate to predicted maximum growth rate was employed as an ecological growth coefficient (EGC) in identifying major determinants of growth for brown trout, Salmo trutta, in natural streams. The coefficient may be more useful than specific growth rate when comparing trout populations from streams having diverse characteristics, since it accounts for the quantitative effects of stream temperature and mean trout weight. The maximum growth rate was generated by translating Elliott's bioenergetic equations into computer models applicable to fish weighing 5–300 g and to stream temperatures of 3.8–21.7 °C. EQMAX is the simpler model and generates only maximum growth rate. TROUT estimates the maximum ration size, maximum growth rate, and a variety of bioenergetic parameters. The EGC for Age I + trout ranged from 60 to 90% in three central New York streams. A relatively low EGC (30–60%) observed for Age II + trout in one stream may have been due to the inefficiency of feeding on small invertebrates. Temperature appears to be a dominant feature governing trout growth in streams. The bioenergetic models may provide useful predictions of the effects of foraging on prey communities by brown trout.


2004 ◽  
Vol 82 (10) ◽  
pp. 1638-1646 ◽  
Author(s):  
Eva Brännäs ◽  
Sara Jonsson ◽  
Kurt Brännäs

When animals face temporally periods of strong intraspecific competition, prior residency, available resources, and their competitive abilities in terms of size and behavioural strategy affect their chances of survival. Density, individual size, and behavioural strategy had the strongest effect on growth. The mean growth rate of both resident and intruding brown trout (Salmo trutta L., 1758) decreased with increasing density, and the largest individuals were the most successful ones independently of the density of prior residency. An aggressive behavioural factor was beneficial at the lowest and intermediate densities, whereas a nonaggressive behavioural factor was beneficial at higher densities. Prior residency had no overall significant effect on growth, as the effect was highly density-dependent. The difference in growth rate between introduced and resident individuals was significant only at high density and low food abundance per individual. The intruders had a significantly lower growth rate at high densities and fewer individuals had a high growth rate. These results suggest that stocking fish at densities exceeding the carrying capacity of the habitat results in fewer individuals that are able to compete for resources than if fewer individuals were stocked. Brood stock can then be used in a more efficient way.


2001 ◽  
Vol 62 (5) ◽  
pp. 935-944 ◽  
Author(s):  
Katriina Lahti ◽  
Anssi Laurila ◽  
Katja Enberg ◽  
Jorma Piironen

1995 ◽  
Vol 52 (10) ◽  
pp. 2159-2167 ◽  
Author(s):  
T. Hesthagen ◽  
O. Hegge ◽  
J. Skurdal ◽  
B. K. Dervo

Native and native-stocked brown trout (Salmo trutta) in Lake Tesse, a regulated hydroelectric reservoir (southern Norway), were spatially segregated according to size: small individuals occurred mainly in the epibenthic habitat and larger individuals mainly in the pelagic habitat. In contrast, all size groups of non-native stocked brown trout were mostly restricted to the epibenthic habitat. Age-specific lengths were generally larger for non-native than for native stocked trout, which were larger than native fish. However, growth rate between age 3 and 4 was significantly lower for non-native stocked fish than for native and native stocked fish. Differences in body length were mainly due to strain but also to some extent to habitat. Native fish had significantly fuller stomachs in the pelagic than in the epibenthic habitat in summer. Epibenthic non-native fish had significantly fuller stomachs than native and native stocked fish in August but not in July. Native and native stocked fish fed mainly on surface insects and planktonic crustaceans in both habitats. We hypothesize that the non-native brown trout stocked in Lake Tesse do not use the pelagic habitat in the home lake and are therefore less adapted to utilize such habitat than populations originating from lakes where pelagic habitat is available.


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