Fish are known for their high phenotypic plasticity in life‐history traits in relation to environmental variability, and this is particularly pronounced among salmonids in the Northern Hemisphere. Resource limitation leads to trade‐offs in phenotypic plasticity between life‐history traits related to the reproduction, growth, and survival of individual fish, which have consequences for the age and size distributions of populations, as well as their dynamics and productivity. We studied the effect of plasticity in growth and fecundity of vendace females on their reproductive traits using a series of long‐term incubation experiments. The wild parental fish originated from four separate populations with markedly different densities, and hence naturally induced differences in their growth and fecundity. The energy allocation to somatic tissues and eggs prior to spawning served as a proxy for total resource availability to individual females, and its effects on offspring survival and growth were analyzed. Vendace females allocated a rather constant proportion of available energy to eggs (per body mass) despite different growth patterns depending on the total resources in the different lakes; investment into eggs thus dictated the share remaining for growth. The energy allocation to eggs per mass was higher in young than in old spawners and the egg size and the relative fecundity differed between them: Young females produced more and smaller eggs and larvae than old spawners. In contrast to earlier observations of salmonids, a shortage of maternal food resources did not increase offspring size and survival. Vendace females in sparse populations with ample resources and high growth produced larger eggs and larvae. Vendace accommodate strong population fluctuations by their high plasticity in growth and fecundity, which affect their offspring size and consequently their recruitment and productivity, and account for their persistence and resilience in the face of high fishing mortality.
Ecological classifications according to the Water Framework Directive (WFD) are presented for a set of 32 large (surface area [75 km 2 ) Finnish lakes. We compared three different approaches: classification according to the strictest biological quality element (One-out, All-out approach, OoAo); numerical integration of biological quality elements (BQE) to determine median scores; and the national classification based on weight-of-evidence (WoE) framework. We also examined the sensitivity of eutrophication metrics to phosphorus concentrations.OoAo classification, the national WoE approach gave similar, downgraded or upgraded status classes. Downgrading was due to the higher weight given to water quality and eutrophication pressures. Upgrading was due to the lower weight given to a single macroinvertebrate metric with poorly represented data. In our opinion, the classification based on the WoE approach produces more realistic status estimates than the OoAo classification. Nevertheless, in practical lake management the evidence from the strictest classification metrics still needs to be thoroughly considered.
The tendency towards two-year cyclicity is considered typical of many Fennoscandian vendace populations, especially in fluctuation of recruitment, based on time series of individual lakes. We used two robust indicators to identify and quantify two-year cycles in vendace population proxy time series at different life-stages -spawning stock biomass (SB), density of newly hatched larvae (LD) and recruitment (REC) -from 22 Finnish lakes. Then we applied Fisher's meta-analytical test to assess the adequacy of the evidence to support the hypothesis that vendace population dynamics include two-year cyclicity. The results supported this hypothesis for REC but not for SB or LD. Yet, the indicators and test are conservative and time-series of SB and LD are shorter than those for REC. The appearance of cycles in REC is associated with high post-recruitment mortality, consequently practically only one spawning per cohort. Cycles may be typical for the recovery period from low abundance period also. Still, some populations with moderate post-REC mortality and non-cyclic SB abundance exhibited cycles in REC. Such dynamics presuppose the existence of more complex regulation based on the interaction of different life stages.
Wild stocks of brown trout, Salmo trutta L., collapsed in Finnish inland waters during the 20th Century because dams prevented upstream migration, and low water quality and stream dredging weakened reproduction. The demise in migratory stocks was coupled with overfishing, mainly by gillnetting on lakes. Consequently, the migratory spawning stocks have diminished to negligible levels. The remaining stocks exhibit restricted immigration and emigration, are supplemented by continuous stocking, and their natural genetic diversity is affected by human activities. In recent years, various recovery actions have been implemented including stream channel restorations, fish passage facilities constructed and stocking of eggs and smolts. Gillnetting has also been regulated by banning certain mesh sizes, and catch-and-release of wild trout is spreading amongst sport fishers. However, these measures seem to be inadequate and almost no recovery of migratory populations has been reported. The problem of by-catch in intensive gillnetting continues to threaten stocks and creates disputes between stakeholders. K E Y W O R D S : by-catch, Finnish Lake District, lake-migrating, overfishing, recovery actions, redd counting.
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