– The spawning period of brown trout (Salmo trutta L.) was studied in the river Castril, southern Spain, by means of redd counts. This mountain stream is located near to the southern limit of the species’ natural distribution range and it shows a highly unpredictable flow regime. The spawning period extended from December to mid‐April and the maximum reproductive activity was in February. These results represent the latest reproduction date and the longest spawning period reported in the literature along the natural distribution range of the species. However, belated spawning in the Castril is congruent with the known latitudinal cline: the lower the latitude, the later the spawning period. Our results, along with a review of the literature on natural populations, also showed that the duration of reproduction is the longer, the lower the latitude. Spawning lasted twice as long in the main stem of the river, which is connected with a reservoir, than in the isolated reaches. These differences may be linked to the influence of the reservoir and to habitat fragmentation. We discuss and support the hypothesis that a long spawning period is an advantage for survival in unpredictable habitats. The belated and protracted spawning period found in river Castril has important implications in fisheries management. A strong research effort is needed in order to fill the critical lack of data on southern brown trout populations.
-The relationship between redd superimposition and spawning habitat availability was investigated in the brown trout (Salmo trutta L.) population inhabiting the river Castril (Granada, Spain). Redd surveys were conducted in 24 river sections to estimate the rate of redd superimposition. Used and available microhabitat was evaluated to compute the suitable spawning habitat (SSH) for brown trout. After analysing the microhabitat characteristics positively selected by females, SSH was defined as an area that met all the following five requirements: water depth between 10 and 50 cm, mean water velocity between 30 and 60 cm s )1 , bottom water velocity between 15 and 60 cm s , substrate size between 4 and 30 mm and no embeddedness. Simple regression analyses showed that redd superimposition was not correlated with redd numbers, SSH or redd density. A simulation-based analysis was performed to estimate the superimposition rate if redds were randomly placed inside the SSH. This analysis revealed that the observed superimposition rate was higher than expected in 23 of 24 instances, this difference being significant (P < 0.05) in eight instances and right at the limit of statistical significance (P = 0.05) in another eight instances. Redd superimposition was high in sections with high redd density. High superimposition however was not exclusive to sections with high redd density and was found in moderate-and low-redd-density sections. This suggests that factors other than habitat availability are also responsible for redd superimposition. We argue that female preference for spawning over previously excavated redds may be the most likely explanation for high superimposition at lower densities.
The operation of small hydroelectric dams built on mountain streams induce changes in stream flow regimes that are manifested not only in the intensity of flow events, but also in the variability and frequency of high-and low-flow episodes. Former studies have shown the influence of flow variability upon the dynamics of a resident brown trout population, especially that related to the stream flow regime during spawning, incubation and emerging periods. As these life-stages are known to determine the population dynamics in further ages, stream flow variability appears to be a major influence on the regulation of a wild brown trout
Most studies on the population dynamics of stream-living salmonids have been conducted at the scale of a reach, a stream or a river basin. This can lead to overestimating the importance of local factors acting on a reduced scale compared to the more general factors that drive the dynamics of several populations. Two models were built on the basis of a data set from 60 sampling stations representing separated populations inhabiting a large heterogeneous area encompassing 18 years of quantifications. Our analyses showed the following: (i) Population growth rate (pgr) of a set of independent brown trout populations can be described by means of a single model; (ii) the youngest and the oldest year classes of these populations seem to be limited by the same constraints; (iii) there is a climatic control of the recruitment because of spring weather conditions, but also the abundance of oldest age class may be controlled by the climate, (iv) there is a nonlinear positive effect of winter North Atlantic Oscillation on pgr; (v) there is a 3-year lagged positive feedback tracing the upward trend of a stock-recruitment curve, and 1-year lagged negative feedback showing the downward trend of the curve; (vi) a strong cohort has a positive effect on the whole population that can be detected throughout the time. Our fitted models allowed to predict the mean population densities at a regional scale with <10% error and shed light onto the main factors and associated ecological processes that control these large-scale dynamics.
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