Water quality assessment using integrated modeling and monitoring in Narva Bay, Gulf of Finland

A coupled three-dimensional hydrodynamic–ecological model was used for the assessment of water quality in Narva Bay during one biologically active season. Narva Bay is located in the south-eastern Gulf of Finland. Narva River with a catchment’s area covering part of Russia and Estonia discharges water and nutrients to Narva Bay. The ecological model includes phytoplankton carbon, nitrogen and phosphorus, chlorophyll a, zooplankton, detritus carbon, nitrogen and phosphorus, inorganic nitrogen, inorganic phosphorus and dissolved oxygen as state variables. Both the hydrodynamic and ecosystem models were validated using a limited number of measurements. The hydrodynamic model validation included comparison of time series of currents and temperature and salinity profiles. The ecological model results were compared with the monitoring data of phytoplankton biomass, total nitrogen and phosphorus and dissolved oxygen. The comparison of hydrodynamic parameters, phytoplankton biomass, surface layer total phosphorus and dissolved oxygen and near-bottom layer total nitrogen was reasonable. Time series of spatially mean values and standard deviations of selected parameters were calculated for the whole Narva Bay. Combining model results and monitoring data, the characteristic concentrations of phytoplankton biomass, total nitrogen and phosphorus and near-bottom dissolved oxygen were estimated. Phytoplankton biomass and total phosphorus showed seasonal variations, of 0.6–1.1 and 0.022–0.032 mg/l, respectively, during spring bloom, 0.1–0.3 and 0.015–0.025 mg/l in summer and 0.2–0.6 and 0.017–0.035 mg/l during autumn bloom. Total nitrogen and near-bottom oxygen concentrations were rather steady, being 0.25–0.35 and 2–6 mg/l, respectively. The total nitrogen and phosphorus concentrations show that according to the classification of Estonian coastal waters, Narva Bay water belongs to a good water quality class.     

Conflicts between biodiversity conservation and human activities in the central and eastern European countries

Conflicts between the conservation of biodiversity and other human activities have been and continue to be of increasing concern in the European Union, often having important political, economic, and environmental repercussions. These conflicts have been addressed in the European Union by using a wide array of top down and bottom up tools, with varying degrees of success. A new challenge is now facing Europe with the integration of 10 new countries in the European Union (EU) and an additional range of biodiversity-rich habitats placed under EU legislation. The rich biodiversity of the central and eastern European countries (CEEC) is likely to be threatened by some aspects of the integration process, and conflicts between the conservation of biodiversity and other human activities are expected. In this paper, we review certain existing conflicts between biodiversity conservation and human activities in the CEEC, expected conflicts associated with integration to the EU, particularly in terms of new policy and legislation implementation, and, finally, explore possible conflict management options.     

Effect of peroxide on neutralization-potential values of siderite and other carbonate minerals

To assess quantitatively the effect of peroxide addition to standard static tests of the neutralization potential (NP) of mine wastes, 10 specimens of carbonate minerals, including five of siderite (FeCO3) and two of rhodochrosite (MnCO3), were analyzed by electron microprobe. The compositions of the siderite span a range from 60 to 86 mol % Fe. Tests of NP for the siderite diluted with 80% (w/w) kaolinite gave values of 647 to 737 kg CaCO3 equivalent per Mg for determinations by the standard Sobek method. However, if it is assumed that the ferrous carbonate component of the mineral does not contribute to NP in field situations because oxidation of Fe(II) to Fe(III) and the subsequent hydrolysis of Fe(III) leads to the release of an equivalent amount of acid, then the calculated NP for the samples ranges from 110 to 390 kg CaCO3 equivalent per Mg. Two different methods involving the addition of peroxide to the test solutions were successful in bringing the measured NP values closer to the theoretical ones. By contrast, the tests with rhodochrosite indicated the Mn(II) to be stable. For long-term environmental planning, especially for wastes from metalliferous sulfide-poor deposits in which gradual dissolution of silicate and aluminosilicate minerals may be involved in attenuating the acidity, consideration in the overall NP budget needs to be given to the ferrous iron content of those minerals. The presence of Fe2+-bearing minerals, especially carbonates, in tested mine-waste materials may lead to overestimated Sobek NP values, thus increasing the risk of poor-quality drainage and the need for costly remediation.