The influence of small-scale variation in habitat on winter trout distribution and diet in an afforested catchment

(1) Habitat influences on trout distribution and diet at a reach scale were analysed over a single winter in a conifer-afforested catchment in Ireland, in an area subject to very low levels of atmospheric pollution. (2) A total of 234 salmonids were sampled from which 1194 individual prey items were recovered. Salmonids were sampled at eleven sites over a 2 km stretch of the river Douglas, a third order stream of the river Araglin in the Munster Blackwater, Co. Cork, Ireland. (3) In this winter study, water depth and flow primarily influenced trout distribution. (4) Stepwise multiple regression was used to identify the most influential environmental factors on trout metrics. Trout biomass was positively correlated to maximum depth and the percentage of pool area within sites, but density and condition were not significantly influenced by habitat variation at the reach scale. (5) The results from diet analysis suggest that trout are heterogeneous generalist feeders in winter, preying mainly on Trichoptera and Ephemeroptera species. Prey diversity in the diet of individuals throughout the study was positively correlated to the percentage of deciduous vegetation, undercut banks and coniferous vegetation, whilst the prey sub-population diversity at site scale was not related to any of the habitat variables measured.     

Re‐building brown trout populations in dredged boreal forest streams: in‐stream restoration combined with stocking of young trout

1. Rivers in boreal forested areas were often dredged to facilitate the transport of timber resulting in channels with simplified bed structure and flow fields and reduced habitat suitability for stream organisms, especially lotic fishes. Currently, many streams are being restored to improve their physical habitat, by replacing boulders and gravel and removing constraining embankments. The most compelling justification behind stream restoration of former floatways has been the enhancement of native fish populations, specifically salmonids. 2. We examined the success of a stream management programme aimed at re‐building diminished brown trout (Salmo trutta) populations by monitoring densities of young‐of‐year and older trout in 18 managed and three reference streams during 2000–2005. Rehabilitation included in‐stream restoration combined with a 5‐year post‐restoration period of stocking young brown trout. Our space‐for‐time substitution design comprised four pre‐management, four under‐management, 10 post‐management and three reference streams. 3. Densities of young‐of‐year brown trout, indicating population establishment, were significantly higher in post‐ compared with pre‐management streams. However, density of young‐of‐year brown trout in post‐management streams was significantly lower compared with near‐pristine reference streams. Furthermore, success of managed brown trout population re‐building varied, indicating stream‐specific responses to management measures. Density of burbot (Lota lota), a native generalist predator, was associated with low recruitment of brown trout. 4. Stream‐specific responses imply that rehabilitation of brown trout populations cannot be precisely predicted thereby limiting application. Our findings support the importance of adaptive stream restoration and management, with focus on identifying factor(s) limiting the establishment of target fish populations.     

Simple predictions of instream habitat model outputs for target fish populations

1. Bottom-up approaches based on individual behaviour can help to identify key variables influencing populations at larger scales. Instream habitat models have been developed to predict the consequences, for populations in stream reaches, of fish preferences for particular hydraulic conditions observed at the scale of individuals. Conventional instream habitat models (e.g. PHABSIM) predict habitat values for species or life stages in reaches, and their changes with discharge. Despite their worldwide use, they have been subject to continuing criticism and have been mainly limited to site-specific case studies.
2. We ran conventional instream habitat models in 58 French stream reaches dominated by brown trout. Using non-linear mixed effect models, we demonstrated that the outputs of instream habitat models (habitat values for three trout life stages and five other species) are predictable from average characteristics of reaches (discharge, depth, width and bed particle size).
3. Our models closely reflect variations in habitat values within-reaches (with discharge) and between-reaches. Within-reach changes are linked to the Reynolds number of reaches, while between-reach changes depend mainly on the Froude number at median daily discharge. These two dimensionless variables combine discharge, mean depth and mean width of reaches. Independent model validations showed robust model predictions that are consistent with studies of habitat values for brown trout made in larger streams from western North America.
4. Our results contribute to identifying the main hydraulic variables governing estimates of fish habitat values. They should facilitate habitat studies in multiple streams, at the basin or larger scales, while reducing their cost. They should enhance the biological validation of habitat model predictions, which remains critical.     

Diurnal shifts in use of summer habitat by age-0 brown trout in a regulated mountain stream

Diurnal shifts in habitat use by age-0 (< 50 mm total length) brown trout (Salmo trutta) were observed from June to July 1989 and 1990 in low-gradient (< 1% channel slope) reaches of Douglas Creek, Medicine Bow National Forest, Wyoming. Fish were visually located during day and night, and water depth, water velocity, distance from the stream edge, substrate, habitat type, and cover were determined at each location. The fish were found predominantly in locations with slow water velocities in stream-margin and backwater-pool habitats. They were observed in slower water, closer to the stream edge at night than during the day.     

Habitat use and life history of brown trout (Salmo trutta) and Arctic charr (Salvelinus alpinus) in some low acidity lakes in central Norway

Habitat utilization and the life history of browntrout Salmo trutta and Arctic charr Salvelinus alpinus were investigated in fivesympatric populations and five allopatric brown troutpopulations in Høylandet catchment, a atmosphaericlow deposition area in Mid Norway. There was asignificant inverse correlation in abundance ofepibenthic Arctic charr and brown trout in theselakes, indicating that the latter species is dominant.The largest numbers of sympatric brown trout andArctic charr were caught in epibenthic habitat. In twolakes, brown trout to some extent also occurredpelagically, while pelagic individuals of Arctic charrwere found in all five lakes. The main food items forboth epibenthic and pelagic brown trout wereterrestrial surface insects and chironomid pupae.Zooplankton was the primary food item for Arctic charrin both habitats. Although the age distribution wasvery different in the populations, neither speciesseem to suffer from recruitment failure. There was nosignificant difference in survival rates betweensympatric populations of brown trout and Arctic charr.We found a significant inverse correlation betweenepibenthic catches of brown trout and the mean weightof 4+ fish, the most abundant age group. However, ifusing weight data for three-year-old fish, no suchrelationship was found for Arctic charr. Brown troutand Arctic charr reached asymptotic lengths of197–364 mm and 259–321 mm, respectively. Both speciestypically reached sexual maturity at age 2–3, and nomaturation-induced mortality was evident. We concludethat fish populations in Høylandet lakes areregulated throughout their lifes by inter- andintraspecific competition.     

Effects of a Severe Flood on the Movements of Japanese Fluvial Sculpin

I studied the movements of adult Japanese fluvial sculpin, Cottus pollux, in a Japanese mountain stream. An exceptionally severe flood in late September had negative impacts on refuge abundance, condition and population density of the sculpin. The mean distance moved monthly correlated positively with water discharge, but not with water temperature or with population density. Overall, the mean distance sculpins moved after the flood was significantly greater than before the flood, and sculpins tended to move into riffle-raceways after the flood. Comparisons of refuge-site limitation for adults and water depths between habitats indicated that the flood affected riffle-raceways less than pools. Fish in poorer conditions were likely to move extensively, and the condition of fish captured initially in pools deteriorated more significantly than that of sculpins captured in riffle-raceways. Movement bias into riffle-raceways by the sculpins after the flood suggests they sought suitable habitat with available refuges. The results suggest vulnerability to flood disturbance of the sculpins inhabiting the interstitial spaces of the substrate.     

Use of three types of stream-margin habitat by age-0 brown trout late in the growing season

The use of stream-margin habitat by age-0 salmonids has been studied, but differences in use among various types of habitat along stream margins has not been addressed. We described the nighttime use of habitat features by age-0 brown trout (Salmo trutta) among three types of stream-margin habitat late in the growing season (August–September) and assessed the extent to which use of habitat features within each type differed over the sampling period. Differences in water depths, water velocities, distances from shore, and substrate at the locations of fish along the margins of pools, the margins of riffles, and in backwaters were studied. Variation in habitat use also was observed during the study period as fish increased in length. Our observations are important considerations when developing habitat suitability criteria for assessment of instream-flow needs of age-0 brown trout.     

Habitat Partitioning in a Patchy Environment: Considering the Role of Intraspecific Competition

Coexistence of many size groups of conspecifics in habitat patches may complicate resource partitioning and increase intraspecific interactions. The objectives of my study were to determine partitioning of habitat among age groups of rainbow trout, Oncorhynchus mykiss, coexisting in pool habitat of a headwater stream, and to determine the role of intraspecific competition for such resource partitioning. The trout population showed size and age specific patterns of habitat use, and trout selected locations based on depth and longitudinal position. This habitat use pattern decreased intraspecific overlap among the trout age groups for use of pool space. I used a removal experiment to determine if two-year old trout constrained habitat use by the smaller conspecifics. Although the experimental results imply that recent intraspecific competition was not present, the absence of competitive exclusion was not clearly demonstrated because of low experimental power. While this study identified habitat partitioning among the trout age groups, it remains unclear whether biotic interactions or size specific requirements were causing the habitat use patterns.     

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     

Stochastic modelling of nutrient loading and lake ecosystem response in relation to submerged macrophytes and benthivorous fish

SUMMARY 1. The strong stabilising effect of increased submerged macrophytes (charophytes) and benthivorous fish reduction on the clear water state was shown for shallow Lake Veluwe and Lake Wolderwijd. 2. The first two links in the chain of relationships from external phosphorus (P) loading to in‐lake total‐P concentrations to chlorophyll a concentrations to water transparency, showed a significant correlation with the areal fraction of coverage with charophytes. Higher coverages lead to (i) lower ratios of the in‐lake total‐P concentration compared with the volume weighted average concentration in the inlet water, indicating a higher retention of P in the presence of charophytes (ii) lower chlorophyll a to total‐P ratios, indicating a positive effect of charophytes on top‐down control of algae, and (iii) higher water transparency because of lower algal turbidity. Transparency further improved as a result of benthivorous fish reduction and a significant positive correlation between non‐algal turbidity and benthivorous fish biomass. 3. A model was developed taking into account the inherent variability in precipitation and uncertainties in the empirical relationships determining phosphorus export from stream catchments and other sources and eutrophication variables in the receiving lakes. The model was used to compute (i) probability distributions for in‐lake total‐P, chlorophyll a and Secchi Disc transparency in relation to the coverage with charophytes and benthivorous fish biomass, and (ii) exceedence probabilities with respect to critical values for in‐lake total‐P and water transparency for several management scenarios. 4. The effects of an expected rise in external nutrient loading on the in‐lake total‐P and chlorophyll a concentrations and on water transparency can be compensated for by two proposed control measures: (i) extended treatment at a waste water treatment plant directly discharging into Lake Veluwe, and (ii) diverting the outlet of a stream draining a catchment with high fertilisation. The minimal internal charophyte coverage needed to sufficiently stabilise the clear water state and to meet with the objective of a summer mean water transparency of at least 1 m was estimated at well over 30% of the lake area, while the benthivorous fish stock should be maintained at the present level of c. 20 kg ha^?1.     

Effects of Large Woody Debris Addition on Stream Habitat and Brook Trout Populations in Appalachian Streams

Large woody debris (LWD) was added to eight streams in the central Appalachians of West Virginia to determine if stream habitat could be enhanced and brook trout (Salvelinus fontinalis) populations increased. Brook trout populations were assessed one year prior to habitat manipulation and 3 years post-habitat manipulation. LWD was added by felling approximately 15 trees per 300 m stream reach. Four of the streams had LWD added to one 300 m reach with 300 m unmanipulated reaches upstream and downstream of the manipulated reach to observe within-stream effects of LWD additions on brook trout density. The remaining four streams had LWD added to three 300 m reaches and these streams were compared to those with only a single 300 m manipulated reach to observe the effects of the extent of habitat manipulation on brook trout density. New pools were formed by the addition of LWD, but overall pool area did not increase significantly in reaches where LWD was added. The relatively high gradient and coarse substrate of these streams may have precluded the added LWD from having a significant influence on stream channel morphology and habitat complexity. No pools were formed in the highest gradient stream, while the stream with the most pools formed had the lowest gradient. Brook trout populations fluctuated following habitat manipulations, and there was no overall effect of the LWD additions on within-stream variability in brook trout density. When there were significant differences among-streams with different extents of LWD additions, those streams receiving LWD additions over a large extent had the greatest brook trout densities. The full potential of added LWD to change stream habitat and influence on brook trout populations may take more time to develop than the 3 years post-manipulation period of this study.     

Recruitment as a driver of production dynamics in stream-resident brown trout (Salmo trutta)

1. The objective was to assess the role of recruitment as a determinant of the production dynamics of stream-resident brown trout ( Salmo trutta ) across replicate habitats of contrasting quality and population attributes. A total of 128-year-classes (YC) at 12 stream sites were examined along four tributaries of the Rio Esva drainage (northwestern Spain).
2. A meta-comparison revealed that growth, density, mortality and production were essentially site-specific. However, when all data were pooled, recruitment (as a delayed density-dependent process) affected both growth and mortality in a way such that individuals in YC with high recruitment grew less and had higher mortality.
3. The value of total YC production recorded covered the global range of variation in the production of stream salmonids reported in the literature. Linear regressions of log-transformed data revealed that 89.0%, 58.9% and 70.7% of the variation in YC density, biomass and production, respectively, were explained by variations in recruitment.
4. The inclusion of growth and mortality, together with recruitment, into a multiple regression increased the variance explained of the total YC production by 13.3%, from 70.7% to 84.0%.
5. The functional relationships between recruitment and the population attributes elucidated in this study appear to provide a useful tool for management applications, including forecasting population status.