Changes in the Selection of Microhabitat by Juvenile Atlantic Salmon (Salmo salar) at the Summer–Autumn Transition in a Small River

1984 ◽  
Vol 41 (3) ◽  
pp. 469-475 ◽  
Author(s):  
D. M. Rimmer ◽  
U. Paim ◽  
R. L. Saunders

Over three summers we used direct underwater observation to examine the summer to autumn differences in seven microhabitat properties of three age-classes of juvenile Atlantic salmon (Salmo salar) in the Little Sevogle River of northeastern New Brunswick. Salmon of all three age-classes occupied a wide range of water depths during summer, but were concentrated mainly in depths of 24–36 cm. In autumn, they occurred in this range almost exclusively. The streambed stones most closely associated with the individual positions of all ages were always <20 cm in summer and mostly (84–92%) <10 cm in diameter. In autumn, all ages were associated with home stones up to 40 cm in diameter, with 65–83% of the stones exceeding 20 cm; the size of home stones selected increased with fish age in autumn. There was no apparent relationship between the water depth and home stone size distributions occupied by all age-classes and available in the stream during either summer or autumn. Summer focal water velocity (velocity at the fish's snout) was predominantly 10–30 cm∙s−1 for 0+, 10–40 cm∙s−1 for 1+, and 30–50 cm∙s−1 for 2+ salmon, but during autumn it was almost always <10 cm∙s−1 for all ages. The bottom and surface water velocities as well as the maximum water velocity within 1 m of fish stations increased with fish age during summer and autumn. At the summer–autumn transition, 0+ salmon selected higher bottom, surface, and maximum water velocities, 2+ salmon selected lower velocities, but selection by 1+ salmon remained unchanged. We view substrate size followed by water depth as the primary properties influencing stream suitability for juvenile Atlantic salmon in autumn.

2003 ◽  
Vol 60 (9) ◽  
pp. 1149-1160 ◽  
Author(s):  
Eva C Enders ◽  
Daniel Boisclair ◽  
André G Roy

Fish activity costs are often estimated by transforming their swimming speed in energy expenditures with respirometry models developed while forcing fish to swim against a flow of constant velocity. Forced swimming models obtained using a procedure that minimizes flow heterogeneity may not represent the costs of swimming in rivers characterized by turbulence and by a wide range of instantaneous flow velocities. We assessed the swimming cost of juvenile Atlantic salmon (Salmo salar) in turbulent flows using two means (18 and 23 cm·s–1) and two standard deviations of flow velocity (5 and 8 cm·s–1). Twenty respirometry experiments were conducted at 15 °C with fish averaging 10 g. Our results confirmed that swimming costs are affected by the level of turbulence. For a given mean flow velocity, swimming costs increased 1.3- to 1.6-fold as turbulence increased. Forced swimming models under estimated actual swimming costs in turbulent flow by 1.9- to 4.2-fold. Spontaneous swimming models overestimated the real cost of swimming in turbulent flow by 2.8- to 6.6-fold. Our analyses suggest that models in which both the mean and the standard deviation of flow velocity are explicitly represented are needed to adequately estimate the costs of swimming against turbulent flows.


2002 ◽  
Vol 59 (2) ◽  
pp. 218-228 ◽  
Author(s):  
Aki Mäki-Petäys ◽  
Ari Huusko ◽  
Jaakko Erkinaro ◽  
Timo Muotka

We constructed generalized habitat criteria for juvenile Atlantic salmon (Salmo salar) based on four river-specific suitability indices for depth, water velocity, and substrate to assess whether habitat criteria for juvenile Atlantic salmon are transferable across rivers. We first tested whether salmon are more likely to occupy higher-quality habitats than generally available in a stream reach based on these composite criteria. We then repeated the same procedure using the river-specific criteria of this study and the generalized habitat suitability criteria of Heggenes. As expected, the river-specific criteria were generally the most effective ones in predicting fish habitat use. However, both of the two generalized criteria also transferred fairly well to the test sites. Viewed across salmon size-classes (<9 cm and >9 cm), the river-specific criteria passed the test in ten of eleven cases (91%), and the two generalized criteria passed in nine (82%) of eleven. Thus, it appears that with respect to summertime habitat criteria for juvenile Atlantic salmon, criteria transference is conceivable at least on a regional scale, and perhaps even on a more "universal" scale.


1983 ◽  
Vol 40 (6) ◽  
pp. 671-680 ◽  
Author(s):  
D. M. Rimmer ◽  
U. Paim ◽  
R. L. Saunders

Autumnal changes in behavior and distribution of three age-classes of juvenile Atlantic salmon (Salmo salar) were determined during 3 yr in the Little Sevogle River of northeastern New Brunswick. In summer, salmon were always observed above the streambed, each holding a station over a single, unshaded stone. About 84% of the entire population occurred in the run habitat-type, 12% in riffles and 5% in pools. Underwater visual censuses showed the salmon to be continuously numerous in summer, but, as soon as water temperature fell to or below 10 °C in autumn, they disappeared from their stations and their visible population decreased by 92–98%. Thereafter, the salmon were found almost exclusively in sheltered substrate chambers beneath surface streambed stones. However, salmon distribution among runs, riffles, and pools (77, 18, and 5%, respectively) did not differ significantly from that in summer. Trapping, marking, and absolute population estimates indicated neither dwindling nor egress of the resident population. Thus, instead of suddenly leaving the river area or moving to another habitat-type at low temperatures, the salmon merely moved from their unsheltered summer stations to sheltered winter stations within the streambed. The results indicate the importance of winter habitat management in managing juvenile Atlantic salmon populations.


1975 ◽  
Vol 32 (9) ◽  
pp. 1652-1656 ◽  
Author(s):  
R. John Gibson ◽  
G. Power

Salmon parr and small brook trout were observed in two stream tanks providing choices of cover. One tank was shallow (24–29 cm) and the other deep (43–50 cm). In the shallow tank brook trout occurred most frequently in shade. When salmon were the sole species, they were most frequently in shade, but were mostly away from shade in the presence of trout. This selection for shade was not evident by either species in the deep tank.


2008 ◽  
Vol 65 (8) ◽  
pp. 1667-1680 ◽  
Author(s):  
A. Jamie F. Gibson ◽  
Heather D. Bowlby ◽  
Peter G. Amiro

We examined relationships between abundance and habitat use in three age classes of juvenile Atlantic salmon ( Salmo salar ) in the Stewiacke River, Nova Scotia, Canada. Using stream gradient as a proxy for habitat quality, we used a double half normal function, modified to include density dependence, to model the relationship between habitat quality and fish density. We found that density was asymmetrically distributed around a similar optimum gradient for all three age classes regardless of abundance. Habitat use was highly density-dependent for age-0 and age-1 juveniles, but not for age-2+ salmon. As abundance of age-0 and age-1 salmon increased, their relative density decreased in low-gradient habitat and increased in higher-gradient habitat, although their absolute density increased in all stream gradient categories. Variation in habitat use was consistent with ideal free theory for age-1 juveniles in high-gradient habitat, but not in low-gradient habitat. Age-2+ individuals appeared not to modify their distribution among habitats, even though increasing competition changes the relative benefit of low-gradient habitat in terms of resource acquisition. In contrast, age-1 individuals responded to increased competition by modifying their distribution along the habitat gradient, even though this may have slightly reduced an individual’s potential for growth.


1995 ◽  
Vol 52 (1) ◽  
pp. 186-196 ◽  
Author(s):  
Ernest R. Keeley ◽  
James W. A. Grant

We observed juvenile Atlantic salmon (Salmo salar) over a wide range of stream conditions and body sizes to determine the relative importance of environmental factors and body size as predictors of territory size. Defended and foraging areas were virtually identical in size. Eighty-eight percent of the variation in territory size was explained by differences in body size and age; territory size increased with body size, but young-of-the-year salmon had relatively larger territories for their body size than older fish. Territory size was inversely related to food abundance, the only significant environmental correlate of territory size, but food only explained an additional 2% of the variation in territory size. Intruder pressure, visual isolation, and current velocity were not significantly related to territory size. The allometric scaling of territory size was consistent with the hypothesis that Atlantic salmon maintain a maximum daily ration of drift flowing over their territory. Atlantic salmon in Catamaran Brook have larger territories than is reported in the literature for other stream-dwelling salmonids of a similar size.


2011 ◽  
Vol 68 (12) ◽  
pp. 2080-2089 ◽  
Author(s):  
Darren M. Ward ◽  
Keith H. Nislow ◽  
Carol L. Folt

Predator effects on prey populations are determined by the number of prey consumed and effects on the traits of surviving prey. Yet the effects of predators on prey traits are rarely evaluated in field studies. We measured the effects of predators on energetic traits (consumption and growth rates) of juvenile Atlantic salmon ( Salmo salar ) in a large-scale field study. Salmon fry were released at 18 sites that encompassed a wide range of predatory slimy sculpin ( Cottus cognatus ) abundance. We sampled salmon after 21 and 140 days to measure salmon growth and estimate consumption using a mass-balance model of methylmercury accumulation. Salmon population density was reduced fivefold at sites with abundant sculpin. Over the early season, salmon consumed less where sculpin were abundant, suggesting that reduced foraging under predation risk contributed to predator-caused mortality. In contrast, over the late season, salmon grew more where sculpin were abundant, suggesting that compensatory growth at reduced salmon population density moderated predator-caused mortality. Predator effects on prey energetics can drive variation in survival and growth, with important consequences for population dynamics.


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