Prey consumption rates and growth of piscivorous brown trout in a subarctic watercourse

Prey consumption rates of piscivorous brown trout Salmo trutta were studied in the Pasvik watercourse, which forms the border between Norway and Russia. Estimates of food consumption in the field were similar to or slightly less than maximum values from a bioenergetic model. The piscivore diet consisted mainly of vendace Coregonus albula with a smaller number of whitefish Coregonus lavaretus . Individual brown trout had an estimated mean daily intake of c . 1·5 vendace and 0·4 whitefish, and a rapid annual growth increment of 7–8 cm year⁻¹. The total population of brown trout >25 cm total length was estimated as 8445 individuals (0·6 individuals ha⁻¹), giving a mean ±  s . e . annual consumption of 1553880 ± 405360 vendace and 439140 ± 287130 whitefish for the whole watercourse. The rapid growth in summer of brown trout >25 cm indicated a high prey consumption rate.     

Early-age changes in oxidative stress in brown trout,Salmo trutta

Fish are often used as models for studies investigating the ability of xenobiotics to induce oxidative stress, though age or developmental stage of the individuals studied has been given little attention. Oxidative stress in other organisms is associated with aging as well as with periods of rapid growth, which occurs in young brown trout. We measured protein carbonyls, 20S proteosome activity and glutathione (GSH) levels in farmed Salmo trutta in four different age groups from 5 months to 3 years. We found an increase in protein carbonyls and a decrease in 20S proteosome activity in both brain and liver tissues of the fish with increasing size and age. Total GSH levels in liver tissue declined as fish aged and the GSSG:GSH ratio increased. Five month and 1 year old trout were treated with paraquat (PQ) to induce oxidative stress. Five month old fish showed no changes in the measured parameters while 1 year old fish had both an increase in protein carbonylation in liver tissue and a decrease in 20S proteosome activity in brain tissue. These results indicate that oxidative stress biomarkers are affected by age or rapid growth in brown trout, and that individuals of different ages respond differently to oxidative stress induced by PQ.     

The brown trout (<Emphasis Type="Italic">Salmo trutta</Emphasis>) in the lake, Øvre Heimdalsvatn: long-term changes in population dynamics due to exploitation and the invasive species,European minnow (<Emphasis Type="Italic">Phoxinus phoxinus</Emphasis>)

Studies of the brown trout (Salmo trutta) population in the Norwegian subalpine lake, Øvre Heimdalsvatn, over a 50-year period have revealed major changes in population dynamics. In 1958, the population density was high, with individuals stagnating in growth at lengths below 30 cm. After heavy exploitation during the years 1958–1969, the number of older fish declined substantially, and growth rates increased significantly. Since 1969, the European minnow (Phoxinus phoxinus) have been observed in the lake, with increasing densities from 1977–1978 to 1999–2000. The age structure of the brown trout population has changed markedly from the 1960s to the period 1993–2006. Annual recruitment significantly declined, from an average number of 3746 individuals in age-class 4 during the period 1958–1966 to an average of 1668 during the period 1993–2006. However, due to lower exploitation rates, the number of old fish was significantly higher in the latter period. The summer diet of brown trout has changed substantially from a dominance of the large crustaceans Lepidurus arcticus and Gammarus lacustris to a high occurrence of European minnows, while L. arcticus has become practically absent from the diet. There was a negative relationship between brown trout biomass and annual length increment. However, despite a brown trout biomass at the same level during the years 1993–2006 as in the 1960s, annual individual growth rates have significantly declined. The reduced recruitment and reduced annual growth rates of the brown trout, as well as changes in the diet, are most likely related to the introduction and establishment of the invasive species, the European minnow.     

A Bioenergetic Analysis of Factors Limiting Brown Trout Growth in an Ozark Tailwater River

We examined prey utilization and energy consumption by brown trout, Salmo trutta, in a cold tailwater (Little Red River, Arkansas, USA; LRR) having low biodiversity and low availability of fish as prey. Stomach content analysis and age estimation were performed on thirty brown trout (10 each of three size classes for a total of 710 trout) collected monthly from an upstream and downstream site over a 1-year period. Diet diversity was low at both sites, as 80% and 70% of all prey consumed by upstream and downstream brown trout, respectively, were isopods. Piscivory (<0.5% of individuals sampled) and consumption of terrestrial invertebrates were rare. There was no relation between diet diversity and trout age, and a very small ontogenetic shift in brown trout diet. Second, we investigated brown trout growth rates relative to prey consumption and temperature. Temperatures and availability of prey were less than required for maximal trout growth. However, prey availability limited trout growth directly, but sub-optimal temperatures probably buffered the effect of this reduced energy consumption by reducing metabolic energy expenditures. Brown trout growth was 54.8–57.0% of the maximum predicted by a bioenergetics model. Instantaneous growth rates for age 1 and adult brown trout were slightly higher for those downstream (0.195) versus those upstream (0.152). Although isopods are abundant within this tailwater to serve as a forage base, the displacement of native fish fauna and subsequent lack of establishment of cold-tolerant forage fish species due to the thermal regime of hypolimnetic release from Greers Ferry Reservoir probably serves as a major barrier to brown trout growth.     

Demogenetic structure of brown trout Salmo trutta Linnaeus, 1758 populations in mountain headwaters: implications for conservation management

A demogenetic analysis based on 7 years of observation (2005–2011) was conducted to examine the population structure of brown trout Salmo trutta in pristine dendritic headwaters. The value of genetic divergence (F_ST) among sampling units ranged from ?0.03 to 0.16. Demographic synchrony was low or moderate, and the average correlation coefficient of population growth between sampling units () ranged from 0.28 to 0.66. No isolation by distance was observed, but genetic divergence was negatively correlated with demographic synchrony among sampling units. Variance in the population growth rate (i.e. local extinction probability) increased with distance from the mainstream and from other sampling units. In contradiction with the usual model of stream‐dwelling salmonids, the upstream sections of headwaters holds only ephemeral subpopulations, whereas the mainstream played a role in the source area of the metapopulation. These findings stress the importance of the mainstream in management conservation for brown trout in low productive mountain headwaters.     

Seasonal and regional infestation characteristics of three ectoparasites of whiting, Merlangim merlangus L., in the North Sea

The colonization by both resident and migrating spawner populations of brown trout and the characteristics of resident and migrating juveniles derived from the two populations have been studied in a brook and its tributary over 4 years. Resident trout spawns mainly in the upstream part of the brook and migrating trout in the downstream part. There are density and growth variations for the two age classes (0+ and 1 +) of juveniles in autumn according to the year and the environment. In the brook, the population of 0 + fish increases from downstream to upstream while the density of other age classes decreases. The migrating juvenile population of the brook changes annually and consists mainly of 1 s (one summer) individuals coming from the upper part. These individuals migrate generally in autumn and winter while young trout produced in the middle and downstream parts of the brook migrate mainly in the spring. The emigration process of the 0 + population decreases markedly from upstream to downstream and appears to be independent of the autumn length and sex ratio. In the tributary, most trout are 0+ years old, the population structure is different, and no migrating fish is observed. The results are discussed and a colonization strategy of the brown trout population in this brook is suggested.     

Juvenile migration in brown trout: a consequence of energetic state

1. We explored the mechanisms determining age and size at juvenile migration in brown trout Salmo trutta L. A ¹³³Cs tracer methodology was used to estimate food consumption of juvenile brown trout in a Norwegian stream, and the energy budgets of early migrants and stream residents were compared.
2. Fast-growing brown trout migrated to the lake earlier and at a smaller body size than slower-growing individuals. The 2+ migrants were significantly larger than those that remained 1 or more years longer in the stream. The 3+ migrants were significantly larger than the 2+ migrants. Some fast-growing males matured in the stream, whereas all females left the stream before maturing sexually.
3. The food consumption and the energy budgets for 2+ migrants were more than four times higher than those of the resident 2+ fish. Total energy allocated to growth was also higher among migrants, and the total metabolic costs were five times higher among migrants than among resident fish.
4. The proportional energy allocation to growth among the 2+ migrants was much lower (about half) than that of those remaining longer in the stream. The reduction in the proportion of energy available for growth from age 1+ to 2+ was larger among migrants (88%) than among resident fish (68%). Reduction in the proportion of energy available for growth is a probable explanation for why migrations are initiated at age 2.
5. Our study supports the hypothesis that fast-growing individuals shift their niche earlier and at a smaller body size than slower-growing individuals because they maintain higher metabolic rates and are energetically constrained at a younger age by limited food resources than slow growers.     

Annual variability in the life-history characteristics of brown trout (Salmo trutta) and Arctic charr (Salvelinus alpinus) in a subalpine Norwegian lake

The annual variability in growth and life history traits of brown trout (Salmo trutta L.) and Arctic charr (Salvelinus alpinus (L.)) in Lake Atnsjøen, a Norwegian subalpine lake, was studied over a period of 13 years (1985–1997). The extent to which life-history characteristics recorded on one occasion can be regarded as representative for the population was explored. We found inter-cohort variation in growth for both species; estimates of asymptotic length (L _∞) in ten cohorts ranged between 225–305 mm (CV = 10.5%) for brown trout and 273–301 mm (CV = 4.1%) for Arctic charr. However, this variation was much lower than inter-population variation for brown trout based on single samples from 169 populations (CV = 24.6%). In Lake Atnsjøen, annual growth increment correlated highly with the number of days warmer than 7?°C (R ²=0.60–0.89) for brown trout, and days warmer than 10?°C (R ²=0.40–0.58) for Arctic charr. Females of Arctic charr were younger at sexual maturity than males, while no such difference was found in brown trout. Generally speaking, early maturing individuals of both species grew faster, particularly from age-2 and onwards, than immature individuals. Early maturing individuals, however, were smaller at maturity than those maturing one year older. Age and size at maturity were significantly correlated with asymptotic lengths only in Arctic charr females.     

Recapture rate and growth of hatchery‐reared brown trout (Salmo trutta v. fario,L.) in Blanice River and the effect of stocking on wild brown trout and grayling (Thymallus thymallus,L.)

Hatchery‐reared adult brown trout, Salmo trutta v. fario L., [215–335 mm standard length (L_S), n = 82] were individually tagged and released into three sections of the Blanice River in May 2007. Wild populations of brown trout and grayling, Thymallus thymallus, L., in these sections and three non‐stocked control sections were also tagged. The recapture rate of hatchery‐reared adult brown trout after 6 months (18%, n = 15) was comparable to that of wild adult brown trout in stocked (15%, n = 14) and control (14%, n = 11) sections. The recapture rates of wild brown trout and grayling after 6 months were higher in control sections than in stocked sections, but the differences were not significant. The movement of recaptured large juvenile wild brown trout from stocked sections was significantly higher (36%) than from control sections (9%). Wild brown trout growth and grayling growth were unaffected by stocking with adult hatchery‐reared brown trout.     

Strontium content of scales as a marker for distinguishing between sea trout and brown trout

Strontium was determined in trout scales from a river where it is often difficult to distinguish between sea trout and resident brown trout by coloration or other visual marks. Sr values were compared with values in scales from brown trout caught above the anadromous stretch of the same river and in scales from a river where sea trout coloration is typical. In the first river, the Sr concentration was generally low, and as a mean only 50 ppm higher in scales from individuals classified as sea trout from the anadromous stretch than in brown trout scales from the upper stretch. There was no consistency between fish coloration and Sr concentration in scales from presumed sea trout on the anadromous stretch. Individuals with a typical sea trout coloration could have a lower concentration of Sr than individuals that were classified as uncertain sea trout by coloration. Fish weight did not seem to influence Sr levels. The mean Sr concentration in scales from the typical sea trout colored population in the second river was 2.8 times higher than that of the anadromous part of the first river. The high variability of Sr concentration in sea trout scales may be explained by differences in individual and population life history. The Sr levels reflect differences in saltwater exposure, either expressed by length of stay or concentration of salt in marine habitats. The study has shown that fish coloration is an inadequate mean to distinguish between resident and migratory trout. Nor is Sr determination of scales alone sufficient, because of low inter-group and high intra-group variability in some rivers. However, Sr values can give valuable information on individual and population migration on a large scale.     

Is there a threshold size regulating seaward migration of brown trout and Atlantic salmon?

We investigated the influence of variation in body size and growth rate on age of smolting in Atlantic salmon and brown trout in four different Norwegian rivers. In Atlantic salmon smolt ages varied between 2 and 6 years, and in brown trout between 2 and 7 years. Smolt age was negatively correlated with parr growth, and positively correlated with smolt size. Age at smolting was more variable in the two northern than the two southern rivers. Smolt sizes and ages were also more variable in brown trout than in Atlantic salmon. Based on the observed variation in smolt size and age, we reject the hypothesis that a threshold size alone regulates age at smolting. Within populations smolt age depends on growth rate so that fast-growing parr smolted younger and smaller than slow-growing parr. We hypothesize that smolt size and age is a trade-off between expected benefits and costs imposed by differences in individual growth rate.     

Age and growth of Siberian sculpin (Cottus poecilopus) and young brown trout (Salmo trutta) in a subalpine Norwegian river

Age, growth and density of Siberian sculpin (Cottus poecilopus) and young brown trout (Salmo trutta) within two sections of River Atna; above Lake Atnsjøen [Section 1 at altitudes between 739 and 715 m] and below Lake Atnsjøen [Section 2 at altitudes between 430 and 370 m] was studied during a 6-year period (1986–91). The water temperature was considerably lower in Section 1 than in Section 2, as the number of days with a water temperature above 10?°C (T _{D ≥ 10?° C} ) from spring to August 1 ranged between 2–26 and 26–52 days, respectively. Juvenile brown trout (age 0+) attained a significantly smaller body size in Section 1 than in Section 2; mean length ±SD was 35 ± 8 mm (ranged 27–46) and 43 ± 7 mm (range 38–46), respectively. In Section 2, there was a highly positive correlation between the body length of 0+ brown trout and mean water temperature in June (p<0.005), and also to some extent in Section 1 (p=0.11). Individuals of age 1+ did not exhibit any such difference, while fish in age group 2+ were larger in Section 1 than in Section 2. By using the number of days with a water temperature between the range 5–10?°C (T _{D ≥ 5 ? 10?° C} ) as test variables, we found a highly positive correlation between the August 1 body length of 0+ brown trout and T _{D ≥ 9}?°C from spring to August 1 in Section 2 (p<0.05), as opposed to T _{D ≥ 7}?°C for trout in Section 1 (p=0.11). Young Siberian sculpin (age 0+ and 1+) also exhibited slower growth in Section 1 than in Section 2, but this was not the case among older specimens. In the year with the lowest temperature measured (1987), no 0+ Siberian sculpin were caught in any of the two sections, indicating that low temperature affects their survival. Both species exhibited large spatial and temporal variation in density. Thus, data on abundance and growth sampled on one occasion at one site can not be regarded as representative for these two fish populations.     

Latitude and altitude differentially shape life history trajectories between the sexes in non-anadromous brown trout

We used two different approaches involving two organizational levels and spatial scales to explore altitudinal and latitudinal variation in life histories of non-anadromous brown trout Salmo trutta. First, we studied the factors influencing the maturation of individuals from populations in northern Spain. Second, we explored the effects of altitude (range 40–1,340 m) and latitude (range 40.6–61.7°N) on longevity, maximum length, length and age at maturity, and fecundity, comparing Spanish and Norwegian populations. Individual maturation was determined by length, age, and sex, and at a given size and age individuals were more likely to mature at higher altitudes. Brown trout lived longer but attained smaller sizes at higher latitudes. Both males and females matured at an older age with increasing latitude, but latitude affected their life-history strategies differentially. Males matured at smaller sizes with increasing latitude and altitude, which may indicate that their maturation threshold depends on the growth potentiality of the river since they compete with other males from the same population. The opposite effects were detected in females. Since female fecundity increases strongly with size there may be a size below which maturation has strong fitness costs. Brown trout are extraordinarily plastic, allowing persistence in a wide variety of environments. In the context of climate change, latitudinally based studies are important to predict potential effects of climate change, especially at the southern edge of species distribution.     

Compensatory response 'defends' energy levels but not growth trajectories in brown trout, Salmo trutta L

Compensatory growth is an organism's reaction to buffer deviations from targeted trajectories. We explored the compensatory patterns of juvenile brown trout under field and laboratory conditions. Divergence of size and condition trajectories was induced by manipulating food levels in the laboratory and then releasing the trout into a river. In the stream, the length trajectories of food-restricted and control fish were parallel, but food-restricted fish exhibited partial compensation for mass and rapid recovery of condition. A laboratory experiment on similar sized fish did not provide evidence for compensatory growth in length or mass. In contrast, data matched the compensatory patterns shown in the stream: length trajectories were parallel and the convergence of mass trajectories ceased as soon as food-restricted fish recovered condition to the level of controls. These results show that (i) brown trout did not compensate for depression in structural growth and (ii) mass recovery was targeted to reinstate condition or energy reserves, but not size at a given age. This does not support the common view that compensatory growth can be a general response to growth depression. Rather, compensation in other salmonids could be related to size thresholds associated with developmental switches at the onset of sexual maturation and migration.     

Performance of juvenile brown trout exposed to fluctuating water level and temperature

Individual daily food intake, mass‐specific growth rate and growth efficiency in groups of juvenile brown trout Salmo trutta were compared in tank experiments with three water level regimes (fluctuating, stable high and low water levels) and two temperature regimes (fluctuating between 10 and 14° C and constant 14° C) to simulate events during hydropeaking in regulated rivers. Fish exposed to high stable water level showed higher food intake and growth rate, and higher or similar growth efficiency than fish exposed to fluctuating or stable low water level. Both groups of slow‐growing and fast‐growing individuals fed less and grew slower at stable low and fluctuating water level than at stable high water level. Furthermore, growth and growth efficiency were lower in brown trout exposed to stable low water level and fluctuating temperature, particularly for groups of fish with slow growth. Temperature did not have any effect at high water level. For groups of fast‐growing fish, there was no difference in growth efficiency between treatments. It is concluded that fluctuating water level and temperature have a potentially detrimental effect on growth in juvenile brown trout and effects are more severe in slow‐ than fast‐growing fish.     

Both Contest and Scramble Competition Affect the Growth Performance of Brown Trout, Salmo Trutta, Parr of Wild and of Sea-ranched Origins

The effect of contest and scramble competition on the growth performance of wild and sea-ranched juvenile (0+) brown trout, Salmo trutta, originating from the River Dalälven, Sweden was scrutinised. In a mirror image stimulation (MIS) experiment, and in a 35000 1 stream-water aquarium the trout was studied for three weeks (20 individuals in each of four replicates). Activity in MIS was correlated with swimming activity in the stream-water aquarium. The MIS results could not be used for predicting any social behaviour patterns or the growth performance of a fish. No behavioural differences between the two strains were noted. However, the sea-ranched strain grew faster than the wild one, both in regard to the RNA/DNA ratio and the weight-specific growth rate. Because the strains had the same genetic background and prior to the experiments were raised under similar hatchery condition, the results of this study suggest that the sea-ranching process selects for faster juvenile growth in brown trout. The ultimate mechanisms underlying the faster growth by the domesticated strain probably involves both contest and scramble competition.     

Aggressive behavior as a mechanism of spatial differentiation of juvenile salmonid fishes (based on Black Sea brown trout Salmo trutta labrax (salmonidae))

Aggressive behavior of hatchery-reared juvenile Black Sea brown trout Salmo trutta labrax at the age of 5.5–6.0 months is investigated. Shortage of suitable territory leads to the separation of the fish into two spatial groups: demersal and pelagic. During the process of spatial differentiation of the fish, the individuals that have not selected permanent habitats (demersal or pelagic) are characterized by the highest aggression level. The duration of the formation of stable spatial differentiation of the fish depends on the stocking density. At a low stocking density (10–45 fish/m²), spatial differentiation is established by the beginning of the second day after the transfer of the fish to new conditions; at a high stocking density (182 fish/m²), it is established approximately by the seventh day. Following the establishment of the (secondary) spatial groups, aggressive acts are registered mainly between the individuals from the same spatial group. A role of aggressive behavior in intrapopulation differentiation of brown trout is discussed.     

Long-term population demographics of native brook trout following manipulative reduction of an invader

Although laboratory studies have provided evidence for negative interactions between brook trout and brown trout, it is unknown how these interactions affect larger scale demographics in a natural setting. We tested the effects of invasive brown trout on brook trout demographics by removing brown trout from a sympatric population using a before–after control-impact study design. The study was conducted across a large stream network for a period of 6 years. Abundance of brook trout increased after brown trout removal primarily as a result of increased recruitment and immigration. Size structure also shifted towards larger individuals as a result of increased growth rates and a decrease in emigration of larger trout. Size at maturity and body condition did not change after brown trout removal. Adult brook trout survival increased during the post-treatment period in both the treatment and control reach. A decrease in flood intensity during the post-treatment time period may have led to increased survival. Adult survival may not be the best metric to use when assessing interactions between trout species, especially when the subordinate species has suitable areas to emigrate.     

Effects of angling on population structure of brown trout,Salmo trutta L., in mountain streams of Northern Spain

Effects of angling exploitation on brown trout populations were assessed by comparing fished sections with close ones unfished for at least 20 years, in mountain streams of Asturias (Northern Spain). Both the fish size and age structure significantly differed among sections in the expected direction according to their exploitation status. The main effects were a significant decrease in age structure complexity (diversity), life span, and percent individuals above the legal limit size in the exploited stocks versus the unexploited ones. Trout above the minimum length limit for fishing (18 cm) averaged 19.47% of the fish caught in the unfished sections (sd = 4.01; n = 5), and 4.72% (sd = 3.46; n = 4) in those subjected to angling. Furthermore, fish older than 4 years represented 39.84% (sd = 8.53) and 1.19% (sd = 1.60) of the catch, respectively. Effects on recruitment (density of young fishes) and growth rates (length at age 1 + to 3 +) were not absolutely consistent, though maximum values were associated with fished sections.     

Mangrove zooplankton of North Queensland,Australia

Food consumption, growth, fish length distributions,population sizes and habitat use of the salmonids intwo lakes in the Høylandet area were studied in1986–89. The allopatric brown trout (Salmotrutta L.) in the tarn Røyrtjønna (27 ha) fed mainlyon organisms at the lake surface , crustaceanplankton, Trichoptera and Chironomidae. Only 5% ofthe trout reached an age of 6 years and a length of25 cm. Sexual maturation started at age 3 and a lengthof 14 cm. Through mark – recapture technique thenumber of trout >10 cm was estimated to 115 ha^-1.Growth, fish length frequencies and sexualmaturation of the sympatric brown trout and Arcticcharr (Salvelinus alpinus (L.)) in LakeStorgrønningen (530 ha) were not much different. TheStorgrønningen charr fed chiefly on zooplankton whichby volume represented 33% for the trout. The foodconsumption of Storgrønningen trout was at maximum inJuly with 2.06 mg food (d.w.) per g live fish and forcharr in September with 1.26 mg food. The maximumsize-independent growth rate of trout was 5.2%day^-1 in late June, and for charr 4.1%day^-1 in late July. Seventy percent of theirseasonal growth took place before 15 August. The charrstayed mainly deeper than 3-4 m, at water temperatures<15 °C. Brown trout stayed mainly the littoralzone and in near surface water of the pelagic. Thenumber of pelagic charr was estimated hydroacusticallyto 50 ind. ha^-1. The charr spawn in thelake. Mean numbers of juvenile trout in the twolargest tributaries were 26 and 48 per 100 m².Their annual length increment was 2.8–3.4 cm. Noindication of acidification or other human inducedimpacts were found. The lakes and their tributariesrepresent complex aquatic systems, representative forpristine oligotrophic Norwegian lowland lakes.John W. Jensen died shortly after easter in 1996