Phylogeography of the Turkish brown trout Salmo trutta L.: mitochondrial DNA PCR‐RFLP variation

In the present study, mitochondrial DNA polymerase chain reaction‐restriction fragment length polymorphism (PCR‐RFLP) assay was used to assess the phylogenetic and phylogeographic relationships among 27 brown trout Salmo trutta populations from Turkey. The complete NADH 5/6 region and a second segment comprising the cytochrome b gene and D‐loop of mtDNA amplified by PCR were digested with six and five restriction enzymes, respectively. A total of 27 haplotypes were observed and divided into three major phylogenetic assemblages, namely Danubian (DA), Adriatic (AD) and a newly proposed Tigris (TI) lineage. The timing of the net nucleotide divergence between the major lineages along with the geological history of Turkey suggested pre‐Pleistocene isolation of the Turkish brown trout and provided evidence that Turkey could be considered as a centre of diversification for these lineages. The average haplotype diversity (0·1397) and the nucleotide diversity (0·000416) within populations were low in comparison to the observed interpopulation nucleotide diversity (0·021266). PCR‐RFLP analysis showed that most of the mtDNA sequence variation found in the Turkish brown trout populations was imputable to differences among lineages. On the other hand, there was also an obvious relationship between geographical distribution of the populations and their clustering. The present study showed that brown trout populations from Turkey are highly divergent and mainly have a unique genetic profile that could be used for conservation and management purposes.     

Estimates of survival of stream-dwelling brown trout using

Estimated monthly apparent survival of stream-dwelling brown trout Salmo trutta in south-east Norway was higher in winter than in summer, and lower in Alpine bullhead Cottus poecilopus sites than in allopatric sites. Apparent survival denotes true survival x local site fidelity. Emigration may also explain differences in apparent survival. All brown trout included in this Study were at least 1 year old.     

Seasonal weather patterns drive population vital rates and persistence in a stream fish

Climate change affects seasonal weather patterns, but little is known about the relative importance of seasonal weather patterns on animal population vital rates. Even when such information exists, data are typically only available from intensive fieldwork (e.g., mark–recapture studies) at a limited spatial extent. Here, we investigated effects of seasonal air temperature and precipitation (fall, winter, and spring) on survival and recruitment of brook trout (Salvelinus fontinalis) at a broad spatial scale using a novel stage‐structured population model. The data were a 15‐year record of brook trout abundance from 72 sites distributed across a 170‐km‐long mountain range in Shenandoah National Park, Virginia, USA. Population vital rates responded differently to weather and site‐specific conditions. Specifically, young‐of‐year survival was most strongly affected by spring temperature, adult survival by elevation and per‐capita recruitment by winter precipitation. Low fall precipitation and high winter precipitation, the latter of which is predicted to increase under climate change for the study region, had the strongest negative effects on trout populations. Simulations show that trout abundance could be greatly reduced under constant high winter precipitation, consistent with the expected effects of gravel‐scouring flows on eggs and newly hatched individuals. However, high‐elevation sites would be less vulnerable to local extinction because they supported higher adult survival. Furthermore, the majority of brook trout populations are projected to persist if high winter precipitation occurs only intermittently (≤3 of 5 years) due to density‐dependent recruitment. Variable drivers of vital rates should be commonly found in animal populations characterized by ontogenetic changes in habitat, and such stage‐structured effects may increase population persistence to changing climate by not affecting all life stages simultaneously. Yet, our results also demonstrate that weather patterns during seemingly less consequential seasons (e.g., winter precipitation) can have major impacts on animal population dynamics.     

Seasonal occurrence of sea lice Lepeophtheirus salmonis on sea trout in two north Norwegian fjords

Seasonal occurrence of the parasitic copepod Lepeophtheirus salmonis (sea lice) was studied from March to December 2001 in two large north Norwegian sill fjords without fish farming activity, the Ranafjord and the Balsfjord. Anadromous brown trout Salmo trutta (sea trout) in both fjords had a low infestation rate during all sampling periods, but followed a seasonal pattern. During early and late winter (November to December and March to April) and spring (May to June), the prevalence varied from 0 to 25% and the abundance was <0·5 sea lice. Adults dominated (92%) during this period, particularly gravid females. In both fjords, the highest prevalence was during September (80–81%, all stages represented). In Ranafjord, the abundance and mean intensity during this month was 6·8 and 8·6 sea lice, respectively, while in Balsfjord it was 3·6 and 4·5 sea lice, respectively. Fish were captured at temperatures down to 1° C and at full strength sea water which is supposed to cause osmoregulatory problems for the fish. This observation has implications for the understanding of high‐latitude sea trout behaviour and can also make the fish more vulnerable to heavy sea lice infestation during this period. It is suggested that winter running sea trout help to maintain a self replicating local population of sea lice within such fjord systems where other possible hosts ( e.g . farmed Atlantic salmon Salmo salar ) are not present during a whole year cycle.     

Seasonal changes in the body composition of young riverine Atlantic salmon and brown trout

The body composition of protein and fat in Atlantic salmon Salmo salar and brown trout Salmo trutta before and after winter was investigated in a temperate, small river, normally ice covered from the middle of November until the end of March. Fat, protein and specific energy declined greatly in winter but were replenished rapidly in spring. Rates of decline were slower for the smallest fish, which also had the lowest specific content of fat, protein, and energy, while the differences in absolute amounts were greatest for the largest fish. The mean specific fat content was reduced by 45–70% during winter, relative to the pre-winter period (September). Mean daily reductions in specific enegy of the larger size groups of brown trout (3·7 × 10⁻³ kJ g⁻¹ day⁻¹) were almost half of the corresponding values for the largest Atlantic salmon (6·3 × 10⁻³ kJ g⁻¹ day⁻¹) during winter. A minor reduction in protein content was found during winter, with mean reductions of 6–10% in comparison to those in September. During spring the fat content was replenished rapidly, particularly for the smallest salmon fry (a threefold increase from April to June). Fat content in the larger salmon and trout increased by about 1·8 times. Based on estimated metabolic rates, digested energy during wintertime may contribute about two-thirds of the brown trout fry's energy demand. For Atlantic salmon, the corresponding value is about 50%. The winter period put considerable stress on the young salmonids living in lotic environments, in particular for the smallest fry with the lowest energy content before winter and the largest losses during winter. This should make the fry more vulnerable to adverse abiotic and biotic factors.     

Evaluation of the contribution of supplemental plantings of brown trout Salmo trutta (L.) to a self-sustaining fishery in the Sydenham River, Ontario, Canada

An autumn planting of 4000 tagged yearling brown trout Salmo trutta (L.) in 1969 resulted in an over-winter survival of 26%, an angler recovery the following year of 8·1 % and made up 22 % of the March, 1970 standing population of the species. August standing populations of brown trout increased from 142 trout/ha (17·6 kg/ha) in 1969 to 360 trout/ha (39·3 kg/ha in 1970 while angler harvest of the species increased from 61 trout/ha (12·7 kg/ha) at a rate of 0·26 fish/h to 89 trout/ha (18·5 kg/ha) at a rate of 0·34/h. Using angler recovery and standing population as criteria the planting contributed substantially to the fishery. Actual contribution of stocked trout however, is questioned after detailed analysis of resident population structure and the potential of natural recruitment. It is suggested that the true benefit of stocked trout may be measured by the presence of those stocked fish in excess of the number of resident trout of that size predictable from a normal length distribution curve in waters with self-sustaining populations. Complexities in evaluating the merits of supplemental plantings of hatchery-reared brown trout to existing stream fisheries are examined.     

Stable isotope profiles of partially migratory salmonid populations in Atlantic rivers of Patagonia

In the present study, profiles of stable isotope composition were characterized for two species with partially migratory populations in rivers along the latitudinal gradient of Patagonia, brown trout Salmo trutta and rainbow trout Oncorhynchus mykiss . The effects of factors ( e.g. ontogeny of fishes, location, species and fasting) that may influence the stable isotope analysis (SIA) were evaluated, as was SIA evaluated as a tool to assign individual fish to their corresponding ecotype. Anadromous fishes exhibited enriched δ¹⁵N (15·2 ± 1·0‰; mean ± s . d .) and δ¹³C (−19·2 ± 1·3‰) relative to resident fishes'δ¹⁵N (8·8 ± 1·1‰) and δ¹³C (−23·2 ± 2·5‰). For both species, the difference in δ¹⁵N was larger between resident (range 6·8–10·7‰) and anadromous (range 14·3–17·8‰) fishes than that in δ¹³C. Values of δ¹³C, while not as dramatically contrasting in rainbow trout, provided a powerful anadromy marker for brown trout in the region. Increases were found in both δ¹⁵N and δ¹³C during the spawning migration of anadromous rainbow trout, most likely due to fasting. Differences in stable isotopes between location, size and species were found, suggesting different stable isotopes base levels in freshwater environments and different trophic levels and feeding location of anadromous populations. The SIA was demonstrated as a powerful tool for ecotype discrimination in Patagonian Rivers, overriding any effect of sampling location, size or species.     

The effect of acid water on the hatching of salmonid eggs

The survival of salmon Salmo salar , sea trout and brown trout Salmo trutta eggs in acid water in the range pH 3·5±7·0 was investigated over a period of three winters. The effects of fertilising the eggs in acid water at pH 4·0, 4·5 and 5·0, and dilution of the test media were also studied. There was considerable yearly variation in the numbers of eggs which hatched, but there were no marked differences between the three species in the tolerances of the eggs to acid water; pH 3·5 was lethal within 10 days to all the eggs, but at pH 4·5 and higher pH levels there was no obvious difference in hatching attributable to acidity.     

Life history characteristics of brown trout in lakes at different stages of acidification

In 66 Norwegian lakes with allopatric populations of brown trout Salmo trutta that ranged from highly acidified to non-acid (pH 4·7–6·6) there was a significant inverse correlation between mean age and relative abundance (CPUE). As mean annual survival rates were not significantly related to CPUE, this population response may indicate that recruitment was lower in low-density lakes. Age-specific masses were significantly higher in populations that had declined in abundance than in unaffected populations. Mean body mass at sexual maturity in both males and females was inversely correlated with CPUE. Between populations, high age at maturity was associated with high survival rates in both sexes. Age at maturity correlated positively with specific growth rate between the ages of 1 and 2 years in females only.     

Influence of sex, body size, and reproduction on overwinter lipid depletion in brook trout

Expressed as percentages of total fresh body weight, lipids of brook trout Salvelinus fontinalis declined between October and April: reproductive males from 2·89 to 1·22%, reproductive females from 3·19 to 1·84%, and non-reproductive males and females from 2·75 to 2·08%. The absolute and proportional overwinter reduction in lipids among reproductive trout was more than twice that of non-reproductive trout, with reproductive males losing significantly more lipids than reproductive females. Larger reproductive individuals lost more lipids during winter, relative to body size, than smaller individuals, although such an effect was not evident among non-reproductive trout. The average overwinter reduction in lipids for reproductive males (58%), females (42%), and non-reproductive trout (24%) was negatively associated with mark-recapture estimates of overwinter survival probabilities of 0·27, 0·36, and 0·58, respectively, providing support for the hypothesis that energy is allocated to reproduction to the detriment of post-reproductive survival. Our emergent hypothesis that reproductive costs differ between sexes, and the life history consequences thereof, merit further study.     

The natural regulation of numbers and growth in contrasting populations of brown trout, Salmo trutta, in two Lake District streams

SUMMARY. 1. This short review summarizes a long-term investigation of brown trout in two populations that probably represent opposite extremes of life histories in this polymorphic species; Bhick Brows Beck serves as a nursery for the progeny of migratory trout (mixture of sea and estuarine trout) and Wilfin Beck is populated by resident trout. 2. Population density in Black Brows Beck was always much higher than that in Wilfin Beck, and was regulated by density-dependent survival in the early stages of the life cycle. There was no evidence for similar density-dependent regulation in Wilfin Beck; simple proportionate survival occurred with fairly constant loss-rates. Survival was reduced in both populations by summer droughts and also by spates in Wilfin Beck. 3. Black Brows trout were always larger than Wilfin Beck trout of similar age; fry size at the start of the growth period was chiefly responsible for these differences. Variations in water temperature were chiefly responsible for differences in growth rates between year-classes within each population. Food intake was not a limiting factor, except in the first winter of the life cycle and for adults over 3 years old in Wilfin Beck. Variation in individual size was inversely density-dependent in Black Brows Beck and decreased with age in Wilfin Beck, these changes being due to natural (stabilizing) selection. 4. There is strong evidence for genotypic differences between the populations. The implications of this are discussed, especially the need to conserve different populations that may contain unique genetic material, and the importance of restocking with fish reared from the indigenous population that should always contain the optimum genotypes for a particular habitat. Restocking with juveniles should be done with caution because it could lead to a decrease in both numbers and size variation when the population is regulated by density-dependent mechanisms. 5. One major objective of future work should be the development and improvement of mathematical models that can be used to predict the optimum density for trout in different populations, the maximum attainable growth rate in different habitats, and the effects on trout populations of environmental changes due to natural causes (e.g. droughts and spates) or human activities.     

Radio-transmitted electromyogram signals as indicators of swimming speed in lake trout and brown trout

Swimming speed and average electromyogram (EMG) pulse intervals were highly correlated in individual lake trout Salvelinus namaycush ( r ²=0·52–0·89) and brown trout Salmo trutta ( r ²=0·45–0·96). High correlations were found also for pooled data in both lake trout ( r ²=0·90) and brown trout of the Emå stock ( r ²=0·96) and Lærdal stock ( r ²=0·96). The linear relationship between swimming speed and average EMG pulse intervals differed significantly among lake trout and the brown trout stocks. This successful calibration of EMGs to swimming speed opens the possibility of recording swimming speed of free swimming lake trout and brown trout in situ . EMGs can also be calibrated to oxygen consumption to record energy expenditure.     

Similarity in seasonal flow regimes,not regional environmental classifications explain synchrony in brown trout population dynamics in France

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Variation in brook and brown trout survival within and among seasons, species, and age classes

The Program MARK was used to generate and test a plausible set of survival models for brook trout Salvelinus fontinalis and brown trout Salmo trutta to determine whether survival differed by season, species or age class. Apparent survival varied with time and age, but not by species. For the older (1999) age class, survival was lowest during the autumn of their age 1+ year whereas survival was lowest for the younger (2000) age class during the early summer of their age 1+ year. Additionally, estimates of survival for the younger age class exceeded those of the older age class in all but one interval (early summer 2001) but significant differences were observed in only one of these intervals (autumn 2000). To determine whether the observed seasonal differences in survival were related to seasonal differences in movement rates, multi‐strata spatial models were used within Program MARK to determine the probability of moving for each interval. In‐site movement rates were found to be low regardless of season (average for all cohorts combined was 5%). The ability of the multi‐strata modelling approach to detect temporal variability in movement, however, was potentially limited by spatial scale of the study reach ( c . 1 km). Differences in survival between different aged fishes could lead to selection acting on age at maturity or reproductive effort at a given age.     

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.     

Seasonal changes in stream salmonid population densities in two tributaries of a boreal river in northern Japan

We examined seasonal changes in population densities of stream salmonids (masu salmon Oncorhynchus masou, white-spotted charr Salvelinus leucomaenis, and rainbow trout O. mykiss) in two tributaries of the Shoro River, eastern Hokkaido, Japan. In one small tributary, water temperature was relatively high during the winter, and populations of salmon and trout increased through immigration at this time of the year, becoming dominant components of the salmonid assemblage; the density of charr in this stream decreased during the winter, but charr was dominant during the summer. In another medium-sized tributary, the water temperature fell to close to 0°C during the winter, and densities of salmon and charr decreased in this season, through emigration; trout were very rare in this stream. Seasonal patterns of stream salmonid densities vary among species and between localities, resulting in seasonal changes in species composition. For a comprehensive understanding of population processes, a whole-river survey across seasons will be necessary.     

Effect of fluctuating flow and temperature on cover type selection and behaviour by juvenile brown trout in artificial flumes

Brown trout Salmo trutta in a flume used cover more often and were more aggregated at low water temperatures in winter compared with summer. Cover combinations providing the most cover (overhead, visual and velocity cover) were preferred in winter whereas velocity refuges were preferred in late summer; and brown trout rarely used any of these cover structures in early summer. Flow affected cover use especially in winter, when most of the trout moved to shelters during the first high flow period. Movements by brown trout were most frequent in early summer. The much higher aggression rate in summer compared with winter decreased during the first period of high flow in both summer experiments. The results indicate seasonal changes in cover habitat and cover type preferences suggesting that habitat complexity is important, and availability of cover is particularly important during different seasons and fluctuating flow.     

Growth, survival and production of juvenile salmon and trout in a Scottish stream, 1966–75

Investigations of the growth, survival and production of young salmon Salmo salar , brown trout and sea trout S. trutta in sections of a stream in Scotland were made during 1966–75. At the end of the growing season, in autumn, the size of the 0+ salmon ranged from a mean weight of 1.12 g in 1966 to 2.82 g in 1973, and the size of the 0+ trout ranged from a mean of 2.20 g in 1966 to 3.56 g (68.0 mm) in 1974. Growth rates of 0+ salmon between July to September were similar from year to year, as was the case with the 0+ trout. The greater size attained in their first year by trout, resulted from the longer feeding season, provided by earlier emergence of fry and ability to continue growing in colder weather in autumn. The lengths attained by 0+ salmon and 0+ trout in September were related to the population densities of 0+ salmon and the number of days above 0° C from 1 December. There was no discernible relationship between lengths of 0+ trout and the population densities of 0+ trout. Salmon and trout lost weight during the winter, which was made up by April. The densities of 0+ salmon in June varied between 2–12m ^–2. Rates of decrease of the population densities in their first year were related to their densities at the beginning of the season, and, more closely, to the densities of salmon and trout combined. At the end of the second year's growth there were between 0.06 and 0.25 salmon m ^–2. Size of the trout populations varied less from year to year than those of salmon. The life of a year class of salmon and trout could be divided into several stages characterized by different rates of decrease of the population.     

Cardiorespiratory status of triploid brown trout during swimming at two acclimation temperatures

At 14° C, standard metabolic rate (75·1 mg O₂ h⁻¹ kg⁻¹), routine metabolic rate (108.8 mg O₂ h⁻¹ kg⁻¹), active metabolic rate ( c . 380 mg O₂ h⁻¹ kg⁻¹), critical swimming speed (U_crit 1·7 BL s⁻¹), heart rate 47 min⁻¹), dorsal aortic pressure (3·2 kPa) and ventilation frequency (63 min⁻¹) for triploid brown trout Salmo trutta were within the ranges reported for diploid brown trout and other salmonids at the same temperature. During prolonged swimming ( c . 80% U _crit), cardiac output increased by 2·3-fold due to increases in heart rate (1·8-fold) and stroke volume (1·2-fold). At 18° C, although standard and routine metabolic rates, as well as resting heart rate and ventilation frequency increased significantly, active metabolic rate and certain cardiorespiratory variables during exercise did not differ from those values for fish acclimated to 14° C. As a result, factorial metabolic scope was reduced (2·93-fold at 18° C v . 5·13-fold at 14° C). Therefore, it is concluded that cardiorespiratory performance in triploid brown trout was not unusual at 18° C, but that reduced factorial metabolic scope may be a contributing factor to the mortality observed in triploid brown trout at temperatures near 18° C.     

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.