The impact of pelagic (Daphnia longispina) and benthic (Dreissena polymorpha) filter feeders on chlorophyll and nutrient concentration

An outdoor experiment testing the effect of water flea (Daphnia longispina) and zebra mussels (Dreissena polymorpha) on physical and chemical water parameters and chlorophyll concentration changes was carried out in 12 containers filled with 150 l of unfiltered water from a lowland reservoir. During the 11 weeks of the experiment, the following physical, chemical and biological measurements were recorded: temperature (°C), oxygen concentration (mg dm⁻³), pH, conductivity (S cm⁻¹), concentration of phosphate phosphorus (PO₄-P) and ammonia nitrogen (NH₄-N) (g dm⁻³), total nitrogen (TN) and total phosphorus (TP) (g dm⁻³), phytoplankton community structure and chlorophyll a concentration (g dm⁻³). The amount of ammonia ions was the highest in the treatment with zooplankton, while phosphate ions reached the highest values in treatments with zebra mussels. The results confirmed the ability of Daphnia to increase the NH₄:PO₄ ratio, whereas excretion from zebra mussels resulted in a decrease in both the N:P ratio (ranging from 9 to 13) and the NH₄:PO₄ ratio in water. In both treatments containing zebra mussels, P-rich water enabled sudden growth of Chlorophyta, resulting in blooms of Hydrodictyon reticulatum after 3–4 weeks of the experiment. Such phenomena were not observed in the control and Daphnia treatments. Our results indicate that zebra mussels, in contrast to Daphnia, may increase the symptoms of water eutrophication and contribute to blooms of expansive phytoplankton species.     

Evaluation of chemical composition changes of surface water in Boguchan Reservoir (Siberia,Russia)

Abstract

Mathematical transformation models of TDS (total dissolved salts) and organic substance concentration as BOD₅ (biochemical oxygen demand) in water of the Angara River and the proposed Boguchan Reservoir have been developed. Having filled the reservoir to a water level of 208 m, in an average year it is shown that increase in surface water mineralization is expected in the cross-section of Boguchan Hydroelectric Power Station giving TDS of up to 20–40 mg/dm³, and values of BOD₅ will increase to 2.0–3.9 mgO₂/dm³. In a low-water year the value of BOD₅ may be as great as 5 mgO₂/dm³; mineralization, in contrast, decreases. Several years after reservoir filling, the values of BOD₅ would decrease, but water quality of the upper part of the reservoir would still depend on the degree of treatment of wastewater discharged to it.

Editor D. Koutsoyiannis

Citation Savichev, O.G. and Matveenko, I.A., 2013. Evaluation of chemical composition changes of surface water in Boguchan Reservoir (Siberia, Russia). Hydrological Sciences Journal, 58 (3), 706–715.     

Kinetics of Exchange-Adsorption Processes in the Formation of Mineral Sulfate Sodium Waters

The ion-exchange properties of terrigenous rocks have been studied, and physicochemical modeling has been used to study the formation of sulfate sodium water in the Volga–Ural Basin of the Russian Plate and the Kartalinskii Basin of the Caucasian hydrogeological folded area. Hydrogeochemical experiments have shown that the exchange-adsorption interaction between gypsum water and adsorbed Na⁺ of terrigenous rocks in the water–rock system involves many stages, resulting in the accumulation in solution of considerable amounts of Na₂SO₄ (up to 9–17 g/dm³).     

Transport of nitrogen in soil water following the application of animal manures to sloping grassland

Abstract

A field experiment was conducted on a sloping grassland soil in southwest England to investigate the downslope transport of nitrogen in soil water following the application of cattle manure, slurry and inorganic fertilizer. Transport of nitrogen (N) species was monitored on hydrologically isolated plots. Manure (50 t ha^?1), slurry (50 m³ ha^?1) and fertilizer (250 kg N ha^?1) were applied in February/March 1992. Subsurface water movement, by both matrix and preferential flow, was the dominant flow route during the experiment. Subsurface and surface nutrient flow pathways were monitored by analysing soil water and surface runoff for NO₃-N, NH₄-N and total N. Subsurface flow chemistry was dominated by NO₃-N, with concentrations usually between 2 and 5 mg NO₃ ?N dm^?3. Differences between fertilizer and manure treatments and the untreated control were not significant. Significantly elevated NO₃-N concentrations were observed in soil water in the buffer zone, indicating the importance of a buffer zone at least 10 m wide between manure spreading zones and an adjacent water course.     

Removal of NO3– from Drinking Water by Electrocoagulation – An Alternate Approach

The present study provides an electrocoagulation method, for the removal of NO₃^– from drinking water using magnesium as the anode and cathode. The experiments are carried out as a function of pH, temperature, and current density. The results show that the maximum removal efficiency of 95.8% was achieved at a current density of 0.25 A/dm², at a pH of 7.0. The adsorption of NO₃^– preferably fitting the Langmuir adsorption isotherm suggests monolayer coverage of the adsorbed molecules. The adsorption process follows a second‐order kinetics model. Thermodynamic studies show that the adsorption was exothermic and spontaneous in nature.     

Products and Kinetics of the OH‐radical‐induced Dealkylation of Atrazine

Hydroxyl radicals, generated radiolytically in N₂O/O₂‐saturated solutions, yield in their reaction with atrazine equal amounts of deethylatrazine and acetaldehyde (40% of OH radical yield) and deisopropylatrazine and acetone (16%), respectively. The precursors of deethylatrazine and acetaldehyde is their Schiff base which hydrolyzes slowly (OH^–‐catalyzed: k = 5.2 dm³ mol^–1 s^–1). The hydrolysis of the Schiff base of deisopropylatrazine and acetone is too fast to be detected. In a pulse radiolysis experiment, the intermediate formed upon OH‐radical attack (k = 3·10⁹ dm³ mol^–1 s^–1) has a strong absorption at 440 nm. It decays in the presence of oxygen (k = 1.3·10⁹ dm³ mol^–1 s^–1), and upon deprotonation [pK_a(peroxyl radicals) ≈ 10.5] the peroxyl radicals thus‐formed eliminate superoxide radicals (k = 2.9·10⁵ s^–1). s‐Triazine itself reacts much more slowly with OH radicals (k = 9.7·10⁷ dm³ mol^–1 s^–1). This can explain, why in the case of atrazine in comparison to other aromatic compounds, e.g. toluene, the addition of the OH radical to the ring (estimated at ca. 40%) is of relatively little importance as compared to an H‐abstraction from (activated) positions of the side groups.     

Origin of Dissolved Organic Carbon Studied by UV‐vis Spectroscopy

Dissolved organic carbon (DOC) distributions in water from Lake Ipê, MS, Brazil, were investigated. The samplings were performed monthly (surface, 1 m depth, and bottom) from June 1999 to June 2000. Absorbance at 285 nm and DOC concentrations in mg dm^—3, p(DOC), were highly correlated for the three depths. 77% of the surface, 85% for 1 m and bottom samples presented a variation between 20 dm³ g^—1 cm^—1 and 50 dm³ g^—1 cm^—1 of A(285 nm)/p(DOC), that characterizes the dissolved organic matter in lake water as essentially fulvic. The ratio A(254 nm)/p(DOC) was also sensitive for fulvic matter, and an A(250 nm)/A(365 nm) = 4 ratio was characteristic of strongly colored waters. The ratios A(436 nm)/p(DOC) for the three depths also showed a significant correlation. The predominance of fulvic acid is explained by environmental characteristics such as the tropical climate, temperatures above 18 °C, and the lake environment. It was demonstrated that the variation in the water carbon content due to different compartments in the lake can be monitored by UV‐vis spectroscopy ratios.     

Removal of Ni(II) Using Cation Exchange Resins in Packed Bed Column: Prediction of Breakthrough Curves

Sorptive removal of Ni(II) from electroplating rinse wastewaters by cation exchange resin Dueolite C 20 was investigated at the temperature of 30°C under dynamic conditions in a packed bed. The effects of sorbent bed length 0.1–0.2 m, fixed flow rate 6 dm³ min^?1, and the initial rinse water concentration (C₀) 53.1 mg L^?1 on the sorption characteristics of Dueolite C 20 were investigated at an influent pH of 6.5. More than 94.5% of Ni(II) was removed in the column experiments. The column performance was improved with increasing bed height and decreasing the flow rate. The Thomas, Yoon–Nelson, Clark, and Wolborska models were applied to the experimental data to represent the breakthrough curves and determine the characteristic design parameters of the column. The sorption performance of the Ni(II) ions through columns could be well described by the Thomas, Yoon–Nelson, and Wolborska models at effluent‐to‐influent concentration ratios (C/C₀) >0.03 and <0.99. Among the all models, the Clark model showed the least average percentage time deviation. The sorptive capacity of electroplating rinse water using Ni(II) was found to be 45.98 mg g^?1.     

Investigations on the Urea Uptake by Phytoplankton in the Baltic Sea

Urea uptake by the planktonic community was studied in the central Baltic Sea in July/August 1987, in March 1988 and in August 1988. Uptake was measured with ¹⁴C-urca incubations. Uptake rates were determined in the range of 0.8 … 5.7 nmol/dm³ · h urea in March and 25.6 … 48.0 nmol/dm³ · h urea in August. Respired CO₂ was found to represent 98 to 99 = of total uptake. Light stimulated urea uptake; parallel dark incubations showing usually 4.5 to 80.0 = of the uptake in the light. These results and size fractionation studies indicated that phytoplankton was dominating urea uptake. Urea proved to be an important nitrogen source for phytoplankton during the regenerated phase of the phytoplankton succession.     

Seasonal biogeochemical and microbiological studies of small lakes in taiga zone of northwestern Russian (Arkhangelsk Province)

The results of biogeochemical and microbiological studies of three small lakes in southwestern Arkhangelsk province are presented. The lakes differ in their morphometric characteristics, thermal and oxygen regimes, and the extent of anthropogenic impact they experience. In the periods of summer and winter stratification, anaerobic water layers with higher phosphates, ammonium, and sulfide sulfur (hydrogen sulfide) are found to form in the bottom horizon of deep-water zones of the lakes. The highest concentrations of sulfide sulfur (150–210 μg dm⁻³) were recorded in the shallow Beloe Lake during winter low-water period, while in summer, sulfide concentration did not differ from those obtained in other lakes (∼10 μg dm⁻³). The abundance of sulfate-reducing bacteria in lake bottom sediments varied from 10 to 100000 cell cm⁻³, and the rate of sulfate reduction process varied from 29 to 3746 μg S dm⁻³ day⁻¹. Seasonal variations were revealed in hydrogen sulfide distribution over the water column and in the rate of sulfate reduction process in the upper horizons of bottom sediments in the examined lakes.     

Method for identification of gasolines in water

It is shown that gasolines in water can be identified by the relative concentrations of the major aromatic components that are most stable and typical of gasolines (references components): meta- + para-ethyltoluenes, 1,3,5-trimethylbenzene, ortho-ethyltoluenes, and 1,2,4-trimethylbenzene. Three most widespread grades of gasoline are used as an example to show that the lower detection limit of gasoline water pollution by chromatographic analysis with dynamic concentration of sample is 0.01 mg/dm³.     

A combined methodology for estimating the potential natural aquifer recharge in an arid environment

ABSTRACT

An innovative methodology that combines an indirect physiography-based method for determining the runoff coefficient at a sub-basin scale and a water balance model applied on a daily time scale was developed to calculate the natural groundwater recharge in three watersheds within the Oum Zessar arid area, Tunisia. The effective infiltration was calculated as part of the water surplus by considering the average available water content (AWC) of soil and an average runoff coefficient for each sub-basin. The model indicates that the sub-basins covered mainly by the “artificial” soils of tabias and jessour, characterized by average AWC values greater than 150 mm, did not contribute to natural groundwater recharge over the 10-year period (2003–2012) considered. The estimated volume for the Triassic aquifer amounted to about 4.5 hm³ year^?1, which is consistent with previous studies. For the Jurassic and Cretaceous aquifers, the estimated volumes amounted to about 200 dm³ year^?1.     

Dynamics of stream nitrate sources and flow pathways during stormflows on urban,forest and agricultural watersheds in central Pennsylvania,USA

Understanding the influence of storm events on nitrate (NO₃^?) dynamics is important for efficiently managing NO₃^? pollution. In this study, five sites representing a downstream progression of forested uplands underlain by resistant sandstone to karst lowlands with agricultural, urban and mixed land‐use were established in Spring Creek, a 201 km² mixed land‐use watershed in central Pennsylvania, USA. At each site, stream water was monitored during six storm events in 2005 to assess changes in stable isotopes of NO₃^? (δ¹⁵N‐NO₃^? and δ¹⁸O‐NO₃^?) and water (δ¹⁸O‐H₂O) from baseflow to peakflow. Peakflow fractions of event NO₃^? and event water were then computed using two‐component mixing models to elucidate NO₃^? flow pathway differences among the five sites. For the forested upland site, storm size appeared to affect NO₃^? sources and flow pathways. During small storms (<35 mm rainfall), greater event NO₃^? fractions than event water fractions indicated the prevalence of atmospheric NO₃^? source contributions at peakflow. During larger storms (>35 mm rainfall), event NO₃^? fractions were less than event water fractions at peakflow suggesting that NO₃^? was flushed from stored sources via shallow subsurface flow pathways. For the urbanized site, wash‐off of atmospheric NO₃^? was an important NO₃^? source at peakflow, especially during short‐duration storms where event water contributions indicated the prevalence of overland flow. In the karst lowlands, very low fractions of event water and even lower fractions of event NO₃^? at peakflow suggested the dominance of ground water flow pathways during storms. These ground water flow pathways likely flushed stored NO₃^? sources into the stream, while deep soils in the karst lowlands also may have promoted NO₃^? assimilation. The results of this study illustrated how NO₃^? isotopes and δ¹⁸O‐H₂O could be combined to show key differences in water and NO₃^? delivery between forested uplands, karst valleys and fully urbanized watersheds. Copyright © 2009 John Wiley & Sons, Ltd.     

Changes in the patterns of inorganic nitrogen and TN/TP ratio and the associated mechanism of biological regulation in the shallow lakes of the middle and lower reaches of the Yangtze River

The changes of NH₃-N, NO₃-N, NO₂-N and TN/TP were studied during growth and non-growth season in 33 subtropical shallow lakes in the middle and lower reaches of the Yangtze River. There were significant positive correlations among all nutrient concentrations, and the correlations were better in growth season than in non-growth season. When TP>0.1 mgL^?1, NH₃-N increased sharply in non-growth season with increasing TP, and NO₃-N increased in growth season but decreased in non-growth season with TP. These might be attributed to lower dissolved oxygen and low temperature in non-growth season of the hypereutrophic lakes, since nitrification is more sensitive to dissolved oxygen and temperature than antinitrification. When 0.1 mgL^?1>TP>0.035 mgL^?1, TN and all kinds of inorganic nitrogen were lower in growth season than in non-growth season, and phytoplankton might be the vital regulating factor. When TP<0.035 mgL^?1, inorganic nitrogen concentrations were relatively low and NH₃-N, NO₂-N had significant correlations with phytoplankton, indicating that NH₃-N and NO₂-N might be limiting factors to phytoplankton. In addition, TN/TP went down with decline in TP concentration, and TN and inorganic nitrogen concentrations were obviously lower in growth season than in non-growth season, suggesting that decreasing nitrogen (especially NH₃-N and NO₃-N) was an important reason for the decreasing TN/TP in growth season. The ranges of TN/TP were closely related to trophic level in both growth and non-growth seasons, and it is apparent that in the eutrophic and hypertrophic state the TN/TP ratio was obviously lower in growth season than in non-growth season. The changes of the TN/TP ratio were closely correlated with trophic levels, and both declines of TN in the water column and TP release from the sediment were important factors for the decline of the TN/TP ratio in growth season.     

Conductivity as a predictor of a total cations and salinity in Ethiopian lakes and rivers: revisiting earlier models

We used regression analyses of water samples from 18 lakes, nine rivers, and one spring in Ethiopia to (a) test the hypothesis that water bodies of relatively higher salinity (K₂₅>1000 μS cm⁻¹) have a different conductivity to salinity relationship than waters of lower salinity (K₂₅ < 1000 μS cm⁻¹), and (b) develop models to predict total cations and salinity from conductivity that can be used for Ethiopian waters and other African aquatic systems of similar chemical composition. We found no statistical difference in the bilogarithmic relationships (total cations vs. conductivity; salinity vs. conductivity) for waters of higher salinity (K₂₅ > 1000 μS cm⁻¹) and waters of lower salinity (K₂₅ < 1000 μS cm⁻¹). However, comparison among our models and models from the literature suggests that developing separate equations for low and high salinity water bodies has some merit. We believe that the equations developed in this study can be used for Ethiopian waters and other African waters within the range of conductivity in this study.     

Hydrological flow paths controlling stream chemistry in Japanese forested watersheds

Water sources and flow paths contributing to stream chemistry were evaluated in four Japanese forested watersheds with steep topography (slopes ≥30°). Stream chemistry during periods without rainfall and during events with less than 100 mm of precipitation was similar to seepage water chemistry, but markedly different from that of soil water which had higher concentrations of NO⁻₃ and Ca²⁺ and lower concentrations of Na⁺ and HCO⁻₃. Also, stream Cl⁻ concentrations in a Cl⁻‐treated watershed did not increase either during events with less than 100 mm of total rainfall or at baseflow conditions, even three years after the Cl⁻ treatment. These results suggest that groundwater within bedrock fissures of Paleozoic strata had a long residence time and was a major contributor to steam water under baseflow conditions and even during small precipitation events (≤100 mm). In contrast, for large precipitation events (≥100 mm), stream chemistry became more similar to soil water chemistry, especially within the steepest watershed. Also, for large precipitation events, stream Cl⁻ concentrations in the Cl⁻‐treated watershed increased markedly. These results suggest that soil water was a major contributor to stream waters only during these large events. Copyright © 1999 John Wiley & Sons, Ltd.     

曝气充氧对城市污染河道内源铵态氮释放的控制

以城市污染河道沉积物和上覆水为研究对象,利用模拟实验方法,探讨不同曝气充氧方式(水曝气EW、底泥曝气ES)对污染河道內源铵态氮(NH4+-N)释放的影响.研究结果发现:从间隙水和沉积物中NH4+-N的削减效果来看,底泥曝气均要优于水曝气;实验结束后,底泥曝气组沉积物与间隙水中NH4+-N含量分别减少63.39%和43.33%,水曝气组分别减少了7.54%和13.98%;从沉积物-水界面NH4+-N的扩散通量变化来看,水曝气组界面通量高于对照组,其变化规律与对照组相似;底泥曝气组沉积物-水界面NH4+-N扩散通量变化过程完全不同于其它两组,在整个试验周期内(除第5 d以外),底泥曝气组的通量低于水曝气组,在第15 d最低,为13.73 mg/(m2.d),仅为水曝气组和对照组的14.68%和19.93%,表明底泥曝气组沉积物NH4+-N的释放潜力低于水曝气组沉积物.     

Soil NO3− storage from oasis development in deserts: Implications for the prevention and control of groundwater pollution

The sources and storage of soil NO₃⁻ in the western Tengger Desert, Northwest China, were explored using water chemistry analysis and stable isotope techniques. In line with the expansion and development of oases, part of the desert has been transformed into cultivated land and artificial forest land. The mean soil NO₃⁻ contents found in areas of cultivated land and artificial forest were 123.06 mg kg⁻¹ and 1.26 mg kg⁻¹, far higher and slightly lower than the background desert soil values, respectively. The δ¹⁵N-NO₃⁻ and δ¹⁸O-NO₃⁻ values in cultivated soils ranged from 1.00 to 11.81 ‰, and from −1.85 to 8.99 ‰, respectively, and the mean mNO₃⁻/Cl⁻ value in cultivated soils was 2.3. These figures would appear to demonstrate that the rapid increase in the nitrate content in soils is principally due to the use of nitrogen fertilizer. Such increases in soil NO₃⁻ storage is likely to promote the leaching of nitrogen into the groundwater where coarsely textured soils exist, the pollution of water sources used for irrigation water, and extreme precipitation events. The δ¹⁵N-NO₃⁻ and δ¹⁸O-NO₃⁻ values in groundwater ranged from 3.72 to 6.54 ‰, and from −0.19 to 12.06 ‰, respectively, mainly reflecting the nitrification of soil nitrogen. These values appeared similar to those measured in the soil water in adjacent areas of cultivated land and vegetated desert, indicating that the groundwater has been affected by both natural and artificial NO₃⁻. Artificial afforestation of desert regions would therefore seem to be a useful way of reducing the threat posed by anthropogenic sources to the circulation of NO₃⁻-N within arid regions, as well as promoting wind sheltering and sand fixation. This study explored the NO₃⁻ storage and groundwater quality responses to oasis development in arid areas in an attempt to provide effective information for local agricultural organizations and agricultural nitrogen management models.     

Carbon input, production and turnover in the interstices of a Lake Tegel bank filtration site, Berlin, Germany

The sandy littoral zone of Lake Tegel (Berlin, Germany) was investigated during 2004–2006 down to sediment depths ≥26 cm to derive a scheme of seasonal carbon turnover under induced bank filtration conditions. Carbon turnover processes were quantified regarding external and internal sources of dissolved and particulate organic matter (DOM and POM), primary production, community respiration, redox potential as well as specific loads of soluble chemical compounds such as nitrogen, iron, manganese and DOC.Over the course of the year, infiltrating DOC decreased by about 13–20% within the upper 26 cm sediment of the infiltration stretch. Gradients of all observed soluble compounds that are highly cross-linked to biological activities were highest in the topmost centimetre. In this depth mass balances (output–input) were negative concerning NO₃-N (−1 mg dm⁻² d⁻¹, summer mean) and DOC (−2 mg dm⁻² d⁻¹, winter mean), respectively, while specific loads of cations such as manganese reached up to 0.2 mg dm⁻² d⁻¹ during summer. Carbon mineralization ranged between 3 and 7 mg C dm⁻² d⁻¹ and was nearly twice as high in summer as in winter. The turnover of the infiltrating DOC contributed maximally 25% in summer to 50% in winter to the entire organic carbon mineralization. Gross and net primary production differed up to a factor of >10, indicating very fast turnover reactions and the predominance of community respiration and mineralization, respectively. The POC in the upper sediment layer (10 cm) temporally varied around 1% sediment d.w.; benthic algae, organic seston input and autumnal leaf fall contributed similar percentages to the POC pool.     

Flocculation–Sedimentation Combined with Chemical Oxidation Process

Flocculation and sedimentation of particles are essential to many environmental and industrial processes. Solid–liquid separation in olive‐oil mill wastewater treatment by means of Fenton system is the key to work continuously and maintain a constant outlet flow of clarified water at the end of the oxidation process. Natural sedimentation is not capable to eliminate the sludge formed. The efficiency of flocculation operation using different flocculants as QG‐2001, QG‐2002, DQGALFLOC‐130H, and Nalco‐77171 was investigated. The optimum dosage of each flocculant, 150, 2.5, 66, and 6 mg dm^?3, respectively, was determined. The results revealed that the best flocculant was Nalco‐77171, which determined 13.5% v/v final sludge separation and 86.5% v/v final clarified water obtained. Kinetics of sludge removal in the transition zone was adjusted to power law, v/v₀ = Kt^ε, where the exponent, ε, varied in the range 0.141–0.670.