24 research outputs found

    Fate of Allochthonous Dissolved Organic Carbon in Lakes: A Quantitative Approach

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    Inputs of dissolved organic carbon (DOC) to lakes derived from the surrounding landscape can be stored, mineralized or passed to downstream ecosystems. The balance among these OC fates depends on a suite of physical, chemical, and biological processes within the lake, as well as the degree of recalcintrance of the allochthonous DOC load. The relative importance of these processes has not been well quantified due to the complex nature of lakes, as well as challenges in scaling DOC degradation experiments under controlled conditions to the whole lake scale. We used a coupled hydrodynamic-water quality model to simulate broad ranges in lake area and DOC, two characteristics important to processing allochthonous carbon through their influences on lake temperature, mixing depth and hydrology. We calibrated the model to four lakes from the North Temperate Lakes Long Term Ecological Research site, and simulated an additional 12 ‘hypothetical’ lakes to fill the gradients in lake size and DOC concentration. For each lake, we tested several mineralization rates (range: 0.001 d−1 to 0.010 d−1) representative of the range found in the literature. We found that mineralization rates at the ecosystem scale were roughly half the values from laboratory experiments, due to relatively cool water temperatures and other lake-specific factors that influence water temperature and hydrologic residence time. Results from simulations indicated that the fate of allochthonous DOC was controlled primarily by the mineralization rate and the hydrologic residence time. Lakes with residence times <1 year exported approximately 60% of the DOC, whereas lakes with residence times >6 years mineralized approximately 60% of the DOC. DOC fate in lakes can be determined with a few relatively easily measured factors, such as lake morphometry, residence time, and temperature, assuming we know the recalcitrance of the DOC

    Planktonic events may cause polymictic-dimictic regime shifts in temperate lakes

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    Water transparency affects the thermal structure of lakes, and within certain lake depth ranges, it can determine whether a lake mixes regularly (polymictic regime) or stratifies continuously (dimictic regime) from spring through summer. Phytoplankton biomass can influence transparency but the effect of its seasonal pattern on stratification is unknown. Therefore we analysed long term field data from two lakes of similar depth, transparency and climate but one polymictic and one dimictic, and simulated a conceptual lake with a hydrodynamic model. Transparency in the study lakes was typically low during spring and summer blooms and high in between during the clear water phase (CWP), caused when zooplankton graze the spring bloom. The effect of variability of transparency on thermal structure was stronger at intermediate transparency and stronger during a critical window in spring when the rate of lake warming is highest. Whereas the spring bloom strengthened stratification in spring, the CWP weakened it in summer. The presence or absence of the CWP influenced stratification duration and under some conditions determined the mixing regime. Therefore seasonal plankton dynamics, including biotic interactions that suppress the CWP, can influence lake temperatures, stratification duration, and potentially also the mixing regime

    Hybridization and its application in aquaculture

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    Inter‐specific hybrids are usually formed by mating two different species in the same genus. They have been produced to increase growth rate, improve production performance, transfer desirable traits, reduce unwanted reproduction, combine other valuable traits such as good flesh quality, disease resistance and increase environmental tolerances, better feed conversion, and increase harvesting rate in culture systems. Hybrids play a significant role in helping to increase aquaculture production of several species of freshwater and marine fishes – for example, hybrid catfish in Thailand, hybrid striped bass in the USA, hybrid tilapia in Israel, and hybrid characids in Venezuela. As the domestication of fish species increases, the possibilities to increase production through appropriate hybridization techniques are ongoing, with a view to produce new hybrid fishes, especially in culture systems where sterile fish may be preferred because of the concern that fish may escape into the open freshwater, marine and coastal environment. Intentional or accidental hybridization can lead to unexpected results in hybrid progeny, such as reduced viability and growth performances, loss of color pattern and flesh quality, and it also raises risks for maintenance of genetic integrity. Appropriate knowledge on the genetic constitution of the brood stock, proper brood stock management, and monitoring of the viability and fertility of the progeny of brood fishes, is thus very crucial before initiating hybridization experiments. In addition, some non‐generic factors, such as weather conditions, culture systems, seasons, and stresses associated with selecting, collecting, handling, breeding and rearing of brood stock and progeny, may influence hybridization success in a wide variety of freshwater and marine fin fishes to a greater extent

    Relationship between critical load exceedances and empirical impact indicators at Integrated Monitoring sites across Europe

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    Critical loads for acidification and eutrophication and their exceedances were determined for a selection of ecosystem effects monitoring sites in the Integrated Monitoring programme (UNECE ICP IM). The level of protection of these sites with respect to acidifying and eutrophying deposition was estimated for 2000 and 2020. In 2020 more sites were protected from acidification (67%) than in 2000 (61%). However, due to the sensitivity of the sites, even the maximum technically feasible emission reductions scenario would not protect all sites from acidification. In 2000, around 20% of the IM sites were protected from eutrophication. In 2020, under reductions in accordance with current legislation, about one third of the sites would be protected, and at best, with the maximum technically feasible reductions, half of the sites would be protected from eutrophication. Data from intensively monitored sites, such as those in ICP IM, provide a connection between modelled critical thresholds and empirical observations, and thus an indication of the applicability of critical load estimates for natural ecosystems. Across the sites, there was good correlation between the exceedance of critical loads for acidification and key acidification parameters in runoff water, both with annual mean fluxes and concentrations. There was also evidence of a link between exceedances of critical loads of nutrient nitrogen and nitrogen leaching. The collected empirical data of the ICP IM thus allow testing and validation of key concepts used in the critical load calculations. This increases confidence in the European-scale critical loads mapping used in integrated assessment modelling to support emission reduction agreements
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