Hydrochemical characteristics of the natural waters associated with the flooding of the Meirama open pit (A Coruñ, NW Spain)

2008 ◽  
Vol 72 (1) ◽  
pp. 399-403 ◽  
Author(s):  
J. Delgado ◽  
R. Juncosa ◽  
A. Vazquez ◽  
I. Falcón ◽  
J. Canal ◽  
...  

AbstractIn December, 2007, after 30 years of operations, the mine of Meirama ceased extraction of brown lignite. Since then operations have begun which will lead to the formation of a big mining lake (~2 km2 surface and up to 180 m deep) after controlled flooding of the open pit. In the process of flooding, both surface and ground waters are involved, each with their own chemical signature. According to the information available, the diversion of surface waters towards the pit hole should lead to the formation of a water body of acceptable quality. However, an unassisted flooding process could eventually form an acidic lake.

1999 ◽  
Vol 39 (10-11) ◽  
pp. 375-382
Author(s):  
Andreja Žgajnar Gotvajn ◽  
Jana Zagorc-Končan

Biodegradation is confirmed as an important mechanism of organic chemicals removal in natural systems. Estimation of biodegradability of chemicals which reach the aquatic environment in significant or even negligible quantities is necessary in assessing the entire hazard associated with their use. The aim of our study was to compare the standardized ready biodegradability assessment test (closed bottle test) and its modifications, employing the basic agreements on test principles of simulation of biodegradation in surface waters, yet no official standard method has been adopted. The standard test was modified using various natural river waters and a variety of nutrient conditions and microbial species trying to simulate the natural environment in the simplified way. Tests were performed with two compounds with different ability to degrade. Experiments indicate that predictability of biodegradation obtained by ready biodegradability assessment tests for surface waters in many cases is not reliable, because of different conditions, which may prevail in surface waters over time and affect biodegradation. However, the use of natural waters in screening tests assures additional information on fate of chemicals in rivers and lakes.


2005 ◽  
Vol 2 (1) ◽  
pp. 56 ◽  
Author(s):  
Sylvia Sander ◽  
Jonathan P. Kim ◽  
Barry Anderson ◽  
Keith A. Hunter

Environmental Context. The bioavailability of dissolved metals in natural waters is directly affected by metal-sequestering agents. These agents include soil-derived matter and compounds released by microorganisms, since copper can support or inhibit aquatic microorganisms depending on concentration. During summer the levels of copper increase in surface waters, an effect intuitively attributable to increased ultraviolet light degrading the sequestering agents more effectively, leading to a concurrent release of the metal. This paper shows that the amount of degradation attributable to light is too low to explain the metal release and that a biological influence may instead be responsible. Abstract. The influence of UVB irradiation on the Cu2+ binding by natural organic ligands in six alpine lakes on the South Island, New Zealand, has been investigated using competitive ligand equilibration with salicylaldoxime and detection by cathodic stripping voltammetry (CLE-CSV). During austral summer 2002–2003 the total dissolved Cu ([Cu]T), the concentration of strong Cu2+-binding ligands ([L]T), and their conditional stability constant K´´ were determined in surface samples of all six lakes. All lakes exhibited appreciable concentrations of a strong Cu2+ binding ligand with similar K´´ values and concentrations always exceeding [CuT], thus dominating Cu2+ speciation. Four lakes (Hayes, Manapouri, Wanaka, Te Anau) showed no appreciable trend in [LT] throughout the summer, whereas in Lakes Wakatipu and Hawea [LT] increased steadily throughout this period. Laboratory UVB irradiation of lake water samples using a 400 W mercury lamp with a Pyrex glass filter (λ > 280 nm) showed that Cu2+-binding ligands are destroyed by UVB radiation, causing [L]T to decrease with a rate of –0.588 nmol L–1 h–1 (r2 0.88). From this we calculate that the in situ ligand destruction rate by UVB in summer for surface waters of these lakes is too small to significantly affect [LT], and conclude that variations in ligand concentrations must result from seasonally variable biological factors.


2018 ◽  
Vol 41 ◽  
pp. 01007
Author(s):  
Yuriy Kutepov ◽  
Aleksandr Mironov ◽  
Maksim Sablin ◽  
Elena Borger

This article considers mining and geological conditions of the site “Blagodatny” of the mine named after A.D. Ruban located underneaththe old open pit coal mine and the hydraulic-mine dump. The potentially dangerous zones in the undermined rock mass have been identified based onthe conditions of formation of water inflow into mine workings. Safe depthof coal seams mining has been calculated depending on the type of water body – the hydraulic-mine dump.


2021 ◽  
Author(s):  
Yuan Tian ◽  
Jianyu Xiao ◽  
Xinjie Zha ◽  
Chengqun Yu

Abstract Although previous studies have been reported between the Kashin–Beck Disease (KBD) epidemic and the hydrochemical characteristics of surface waters, the etiology of the disease remains unclear. In the present study, we investigated the relationship between the KBD and the environment by comprehensively examining the hydrochemical characteristics of surface waters in Longzi County, Tibet, and the spatial incidence of the disease. Results show that, the pH (mean = 7.27±0.30), TH (mean = 57.08±45.74 mg L–1), and TDS (mean = 67.56±44.00 mg L–1) of surface waters in KBD endemic areas are lower than for those in the non-KBD endemic areas (means of pH = 7.49±0.30; TH = 262.06±123.29 mg L–1; TDS = 253.25±100.39 mg L–1). These results suggest that long-term consumption of low TDS, essential trace elements (e.g., nickel, cobalt, iron, selenium, zinc, molybdenum, and iodine) deficient, and potential toxic elements (such as arsenic) enriched waters by humans likely causes the KBD. Environmental factors such as the geology and geomorphology may produce biogeochemical imbalance, geomorphic, vegetation types and local climatic conditions may have significant impact on food fungi toxin poisoning and water organic compound poisoning, and these are also important in the KBD occurrence.


2019 ◽  
Vol 98 ◽  
pp. 01036
Author(s):  
Larisa A. Nichkova ◽  
Dmitry A. Novikov ◽  
Anatoliy V. Chernykh ◽  
Fedor F. Dultsev ◽  
Galina A. Sigora ◽  
...  

The paper discusses the pioneering results of comprehensive hydrogeochemical studies of natural waters of the Baydar valley (southwestern parts of the Crimean Peninsula), whose major aquifers are confined to the upper Jurassic sediments (karst limestone) representing the most important hydrogeological feature of the study area. Fresh and ultra-fresh waters of predominantly bicarbonate calcium composition with total mineralization in the range from 194 to 1137 mg/dm3 are most widespread in the region. The analyzed waters (surface, ground and artesian) differ significantly in chemical composition and their basic characteristics have been arranged in the following patterns: mineralization of 254-832 mg/dm3 and neutral pH (6.98-7.54) for artesian waters; higher mineralization level (up to 1137 mg/dm3) and wide variations of pH values (from 7.18 to 8.31) for ground waters; mineralization from 194 to 288 mg/dm3 and a slightly alkaline pH (between 8.02 and 8.04) for surface waters collected in the Chyornaya river basin and Chernorechensk reservoir. The studied waters display a unique spectrum of trace elements and REE distribution.


2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Keisuke Fukushi ◽  
Yasuhito Sekine ◽  
Hiroshi Sakuma ◽  
Koki Morida ◽  
Robin Wordsworth

Abstract Salinity, pH, and redox states are fundamental properties that characterize natural waters. These properties of surface waters on early Mars reflect palaeoenvironments, and thus provide clues on the palaeoclimate and habitability. Here we constrain these properties of pore water within lacustrine sediments of Gale Crater, Mars, using smectite interlayer compositions. Regardless of formation conditions of smectite, the pore water that last interacted with the sediments was of Na-Cl type with mild salinity (~0.1–0.5 mol/kg) and circumneutral pH. To interpret this, multiple scenarios for post-depositional alterations are considered. The estimated Na-Cl concentrations would reflect hyposaline, early lakes developed in 104–106-year-long semiarid climates. Assuming that post-depositional sulfate-rich fluids interacted with the sediments, the redox disequilibria in secondary minerals suggest infiltration of oxidizing fluids into reducing sediments. Assuming no interactions, the redox disequilibria could have been generated by interactions of upwelling groundwater with oxidized sediments in early post-depositional stages.


2020 ◽  
Vol 12 (13) ◽  
pp. 5394
Author(s):  
Asterios Laskaridis ◽  
Ioannis Sarakatsianos ◽  
Nikolaos Tzollas ◽  
Ioannis A. Katsoyiannis

Arsenic (As) and chromate (Cr(VI)) contamination of ground and surface waters is a major problem worldwide. Given that a new drinking water limit is anticipated for Cr(VI) and that the limit of arsenic in drinking water is quite low (10 μg/L), there is an urgent need for evaluating technologies that could be efficient for removal of both contaminants simultaneously. In this work, the use of Fe(II) redox assisted coagulation was investigated to simultaneously remove the contaminants of interest. The basic principle of this technology is that Fe(II) could react with Cr(VI) and form Fe(III)-hydroxides and insoluble Cr(III) species, while the freshly formed Fe(III) hydroxides are very efficient adsorbents for As(V). The effect of pH, the water matrix composition, Fe(II) dose, initial contaminant concentrations, NOM presence and phosphate concentration were the examined parameters. The results revealed that with a dose of 2 mg/L Fe(II), residual As(V) and Cr(VI) concentrations were both below 10 μg/L, from initial concentrations of 50 μg/L. Though, this is effective only at circumneutral pH values. This is however not a big obstacle, since most natural waters, especially groundwaters, have near neutral pH values. At these pH values, residual iron concentration was far below 200 μg/L. The presence of phosphate anions inhibited As(V) removal but had no effect on Cr(VI) removal. Increasing Fe(II) concentrations eliminated the effect of phosphate and provided simultaneous phosphate removal. Therefore, Fe(II) coagulation can be applied, with secured results, for simultaneous As(V), Cr(VI) and phosphate removal from waters.


2019 ◽  
Vol 98 ◽  
pp. 01038
Author(s):  
Dmitry A. Novikov ◽  
Larisa A. Nichkova ◽  
Anatoliy V. Chernykh ◽  
Fedor F. Dultsev ◽  
Alexander N. Pyryaev ◽  
...  

Results of the study of the stable isotopes (δ18O, δD and δ13C) distribution in natural waters of the Baydar valley (southwestern part of the Crimean Peninsula) are presented. The study region holds fresh and ultra-fresh waters of predominantly bicarbonate calcium composition with TDS varying from 194 to 1137 mg/dm3. The research results revealed that all of the studied waters are of atmospheric origin that lie either along the global (GMWL) or local (LMWL) meteoric water lines. The established variations are: from -9.5 to -5.6‰ for δ18O values in waters with δD values varying from -64.0 to -40.0‰. The source for bicarbonate ion enriched in δ13C in natural waters of the Bauydar valley are carbonate sedimentary rocks, atmospheric carbon dioxide and organic compounds. Surface waters have heavier isotopic composition δ13C (-9.2 – -7.0‰) because of the atmospheric CO2. Artesian waters are differentiated by lighter δ13C (-12.8 – -10.7‰) due to the interactions between carbonate rocks and the dispersed organic matter. Water sources (springs, wells) are characterized by the widest variations of δ13C (-6.9 – -15.5‰) due to the presence of the atmospheric CO2 and intense processes of biochemical decomposition of organic compounds in the soil layer.


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