ALBERT

Notes: Abstract– Habitat is important in determining stream carrying capacity and population density in young Atlantic salmon and brown trout. We review stream habitat selection studies and relate results to variable and interacting abiotic and biotic factors. The importance of spatial and temporal scales are often overlooked. Different physical variables may influence fish position choice at different spatial scales. Temporally variable water flows and temperatures are pervasive environmental factors in streams that affect behavior and habitat selection. The more frequently measured abiotic variables are water depth, water velocity (or stream gradient), substrate particle size, and cover. Summer daytime, feeding habitats of Atlantic salmon are size structured. Larger parr (〉7 cm) have a wider spatial niche than small parr. Selected snout water velocities are consistently low (3–25 cm. s−1). Mean (or surface) water velocities are in the preferred range of 30–50 cm. s−1, and usually in combination with coarse substratum (16–256 mm). However, salmon parr demonstrate flexibility with respect to preferred water velocity, depending on fish size, intra- and interspecific competition, and predation risk. Water depth is less important, except in small streams. In large rivers and lakes a variety of water depths are used by salmon parr. Summer daytime, feeding habitat of brown trout is also characterized by a narrow selection of low snout water velocities. Habitat use is size-structured, which appears to be mainly a result of intraspecific competition. The small trout parr (〈7 cm) are abundant in the shallow swift stream areas (〈20–30 cm depths, 10–50 cm. s−1 water velocities) with cobble substrates. The larger trout have increasingly strong preferences for deep-slow stream areas, in particular pools. Water depth is considered the most important habitat variable for brown trout. Spatial niche overlap is considerable where the two species are sympatric, although young Atlantic salmon tend to be distributed more in the faster flowing and shallow habitats compared with trout. Habitat use by salmon is restricted through interspecific competition with the more aggressive brown trout (interactive segregation). However, subtle innate differences in behavior at an early stage also indicate selective segregation. Seasonal changes in habitat use related to water temperatures occur in both species. In winter, they have a stronger preference for cover and shelter, and may seek shelter in the streambed and/or deeper water. At low temperatures (higher latitudes), there are also marked shifts in habitat use during day and night as the fish become nocturnal. Passive sheltering in the substrate or aggregating in deep-slow stream areas is the typical daytime behavior. While active at night, the fish move to more exposed holding positions primarily on but also above the substrate. Diurnal changes in habitat use take place also in summer; brown trout may utilize a wider spatial niche at night with more fish occupying the shallow-slow stream areas. Brown trout and young Atlantic salmon also exhibit a flexible response to variability in streamflows, wherein habitat selection may change considerably. Important topics in need of further research include: influence of spatial measurement scale, effects of temporal and spatial variability in habitat conditions on habitat selection, effects of interactive competition and trophic interactions (predation risk) on habitat selection, influence of extreme natural events on habitat selection use or suitability (floods, ice formation and jams, droughts), and individual variation in habitat use or behavior.

Notes: Biochemical and tissue-composition indices were used to determine the impacts of temporary feeding reductions on juvenile Atlantic salmon (4.2g initial weight). Three levels of food reduction (fasting, 20% of control, 50% of control) lasting for 2, 4 or 8 days were compared to a control group (constant feeding at 2.75% of body weight day−1). Ornithine decarboxylase (ODC) activity and RNA concentrations were used to measure changes in protein synthesis; condition factor (K), liver-somatic index (LSI), visceral-somatic index (VSI), and gut index (GI)were used to provide information on stored energy levels. Results showed that physiological adjustments to decreases or increases in feeding occur very quickly. The most rapid responses were changes in ODC activity (within 2 days) and LSI (2–4 days). Changes in RNA concentrations and K required 4–8 days. There was no apparent effect of the treatments on VSI or GI. Temporary reductions of feeding lasting 2 days or less would not be detected by any index except ODC activity. Changes in the indices are discussed with respect to short-term changes in rates of protein synthesis and energy storage.

Notes: Abstract– The diet composition, movcments and growth of Atlantic salmon parr rearing in the estuary of Western Arm Brook, Newfoundland were compared with those of parr from riverine habitats over 2 years. Estuarine parr consumed a variety of prey, including many freshwater taxa (mainly insects), which indicated a dependence on freshwater drift from the river. Prey of estuarine origin (amphipods and sticklebacks) were increasingly consumed between spring and autumn. Prey volume per fish and number of prey per fish increased significantly for estuarine parr between spring and autumn, suggesting an improvement in food availability. Riverine parr, however, realized a general decrease in both parameters between spring and autumn. The recapture of 16% (n= 131) of the 829 parr marked in the estuary in 1987 and 1988 indicated a directed movement toward the head of the estuary and river mouth, as also suggested by the diet analysis. Parr from outer estuary sites were very mobile compared with parr from the estuary site closest to the river mouth, which behaved more like parr in the river proper in displaying strong site fidelity. Movement patterns of parr were primarily along the shoreline. Individual growth rates were highly variable in both environments but especially in the estuary. The mean growth of estuarine parr was 0.23 mm. d−1 between May and October with some evidence of fastest growth having occurred in late spring and early summer (approx. 0.4 mm. d−1); mean growth rate of riverine parr was slower, at 0.12 mm. d−1. The results are discussed in the context that estuarine rearing by salmon parr represents an alternative life-history tactic for the species in river systems in eastern Canada.

Notes: Brook trout, Salvelinus fontinalis, were sampled from two sites on the Koksoak River system in northern Quebec to determine seasonal physiological changes in hematology and proximate body composition. Water content increased over the winter at both sites, whereas body lipids decreased. The relationship was most pronounced in the anadromous trout of the Caniapiscau River compared with the smaller resident trout of a tributary stream. Serum protein levels decreased significantly over the winter with the greatest depletion being realized by Caniapiscau River trout. Despite the severity of the winter stream environment in the north, the extent of depletion was similar to that encountered in temperate latitudes, suggesting compensatory physiological mechanisms within the species’ latitudinal range. By mid-summer both populations had restored their depleted energy stores, especially the anadromous trout which accumulated the greatest amount of lipids after feeding in the estuary. Serum glucose levels were maintained at high levels during the winter, then declined in the summer. Differences between the two sites for the degree of physiological change are discussed in relation to specific overwintering strategies and life history variation.

Notes: Levels of tryptophan (TP), serotonin (5-hydroxytryptamine, 5HT) and 5-hydroxyindoleacetic acid (5HIAA) have been determined in the brains of wild brook trout, Salvelinus fontinalis (Mitchill), and brown trout, Salmo trutta L., using high performance liquid chromatography with electrochemical detection. Immediately prior to spawning, adult female brook trout exhibit higher levels of 5HT in the brain than adult males, immature brook trout and immature brown trout. After spawning, the highest levels of TP are found in spent males, which also have higher levels of 5HT in the brain than spent females and immature brook trout. Immature brook trout exhibit higher levels of 5HIAA than prespawning adults. This difference disappears after the spawning season. Serum protein levels and condition factors are lower in spent female brook trout; however, haematocrit values for both sexes remain unchanged after spawning.

Notes: The feeding of brook and brown trout in a temperate Canadian stream was studied over two winters. Stomach analyses indicate that feeding continues throughout the winter. Both species had similar diets. Despite continuous feeding, condition factors declined significantly in early winter and remained low until the spring, suggesting an early-winter depletion of lipid reserves. Energy (calorific) intake was similar in winter to that found in late summer or spring and therefore was not the cause of low winter condition. The derived energy from feeding was insufficient to offset the costs of maintenance metabolism in the early winter period, for both immature and recently spawned fish. It is suggested that stream-dwelling trout suffer a metabolic deficit during acclimation to rapidly declining water temperatures in November/December. Such a phenomenon has important physiological implications for overwinter survival.