Study on Nitrogen Dynamics at the Sediment–Water Interface of Dongting Lake,China

Eutrophication of lakes and reservoirs has become a worldwide environmental problem, and nitrogen (N) has been recognized as one of the key factors responsible for eutrophication. Nitrogen adsorbed on sediments may be released via chemical and biological processes under changing environmental conditions. Spatial distributions of concentrations of ammonia nitrogen (NH₄ ⁺–N), nitrate nitrogen (NO₃ ^?–N) and total nitrogen (TN) were investigated in sediments and overlying water of Dongting Lake, the second largest freshwater lake in China. The concentration of TN in the sediments exhibited strong spatial variation with relatively high values in the eastern part and relatively low values in the southern part of the lake. The TN concentration in the water of different regions of Dongting Lake was affected by the internal load of sediment N. The vertical distribution of TN in sediment cores showed a decreasing trend with an increase in depth. Concentrations of NH₄ ⁺–N in the sediment cores decreased with the depth increase until 6–8 cm and then increased slowly. However, concentrations of NO₃ ^?–N in the sediment cores showed an opposite trend from those of NH₄ ⁺–N. A kinetic release experiment of NH₄ ⁺–N showed that the maximum release rate occurred in the first 5 min and the amount of NH₄ ⁺–N release reached 77.93–86.34 % of the total amount in 0–10 min. The release of NH₄ ⁺–N in the surface sediments of Dongting Lake fits a first-order kinetics function.     

Reciprocal influence of Kürtün Dam and wastewaters from the settlements on water quality in the stream Harşit,NE Turkey

This paper aims to reveal the reciprocal influence of Kürtün Dam and wastewaters from the settlements on the water quality in the stream Har?it, NE Turkey. Several key water-quality indicators were measured: water temperature (T), pH, dissolved oxygen (DO), electrical conductivity, water hardness, chemical oxygen demand (COD), ammonium nitrogen (NH₄ ⁺–N), nitrite nitrogen (NO₂ ^?–N), nitrate nitrogen (NO₃ ^?–N), total Kjeldahl nitrogen (TKN), total nitrogen (TN), orthophosphate phosphorus (PO₄ ^3?–P), and methylene blue active substances (MBAS). The monitoring and sampling studies were conducted every 15 days from March 2009 to February 2010 at two stations selected in the upstream and downstream of the Kürtün Dam. It was concluded that the Kürtün Dam Lake had a high-quality water in terms of T, pH, DO, COD, NH₄ ⁺–N, NO₂ ^?–N and NO₃ ^?–N values, but slightly polluted water with respect to TKN, PO₄ ^3?–P, and MBAS according to the Turkish Water Pollution Control Regulation. The dam improved the stream water quality by increasing the DO concentration, and decreasing the NO₂ ^?–N and PO₄ ^3?–P concentrations thanks to its hydraulic residence time despite the wastewater discharge by the nearby settlements. However, the wastewater discharge deteriorated the stream water quality increasing the COD, NH₄ ⁺–N, NO₃ ^––N, and TN concentrations.     

Nitrogen and oxygen isotopic compositions of water-soluble nitrate in Taihu Lake water system, China: implication for nitrate sources and biogeochemical process

The stable isotope nitrogen-15 (¹⁵N) is a robust indicator of nitrogen (N) source, and the joint use of δ¹⁵N and δ¹⁸O–NO₃ ^? values can provide more useful information about nitrate source discrimination and N cycle process. The δ¹⁵N and δ¹⁸O–NO₃ ^? values, as well as major ion tracers, from Taihu Lake in east China were investigated to identify the primary nitrate sources and assess nitrate biogeochemical process in the present study. The results show that the nitrate concentration in West Taihu Lake (WTL) was generally higher than those in East Taihu Lake (ETL) and its upstream inflow rivers. The NO₃ ^?/Cl^? value combined with mapping of δ¹⁵N–NO₃ ^? and NO₃ ^? concentration suggest that the mixing process should play a major effect in WTL, and denitrification was the dominant N transformation process in WTL. A linear relationship of close to ~1: 2 was observed between δ¹⁵N–NO₃ ^? and δ¹⁸O–NO₃ ^? values in WTL, confirming the occurrence of denitrification in WTL. The δ¹⁵N–NO₃ ^? data imply that sewage and manure were the principal nitrate sources in WTL and its feeder rivers, while the nitrate in ETL might derive from soil organic nitrogen and atmospheric deposition. The δ¹⁸O–NO₃ ^? data indicate most of nitrate from microbial nitrification of organic nitrogen matter possibly make a significant contribution to the lake.     

Effect of soil-applied calcium carbide and plant derivatives on nitrification inhibition and plant growth promotion

The aim of this study was to evaluate the relative performance of three nitrification inhibitors (NIs) viz. calcium carbide (CaC₂), and plant derivatives of Pongamia glabra Vent. (karanj) and Melia azedarach (dharek) in regulating N transformations, inhibiting nitrification and improving N recovery in soil–plant systems. In the first experiment under laboratory incubation, soil was amended with N fertilizer diammonium phosphate [(NH₄)₂HPO₄] at a rate of 200 mg N kg^?1, N + CaC₂, N + karanjin, and N + M. azedarach and incubated at 22 °C for 56 days period. Changes in total mineral N (TMN), NH₄ ⁺–N and NO₃ ^?–N were examined during the study. A second experiment was conducted in a glasshouse using pots to evaluate the response of wheat to these amendments. Results indicated that more than 92 % of the NH₄ ⁺ initially present had disappeared from the mineral N pool by the end of incubation. Application of NIs i.e., CaC₂, karanjin, and M. azedarach resulted in a significant reduction in the extent of NH₄ ⁺ disappearance by 49, 32, and 13 %, respectively. Accumulation of NO₃ ^?–N was much higher in N amended soil 57 % compared to 11 % in N + CaC₂, 13 % in N + karanjin, and 18 % in N + M. azedarach. Application of NIs significantly increased growth, yield, and N uptake of wheat. The apparent N recovery in N-treated plants was 20 % that was significantly increased to 38, 34, and 37 % with N + CaC₂, N + karanjin, and N + M. azedarach, respectively. Among the three NIs tested, CaC₂ and karanjin proved highly effective in inhibiting nitrification and retaining NH₄ ⁺–N in the mineral pool for a longer period.     

Spatial variations and distributions of phosphorus and nitrogen in bottom sediments from a typical north-temperate lake,China

Concentrations and vertical distributions of total nitrogen (TN), total phosphorus (TP) and their different forms in sediments obtained from nine locations of Lake Dalinouer in September 2008 were analyzed. The results demonstrated that TP in surface sediments ranged from 0.493 to 0.904 g/kg, and inorganic phosphorus was the main fraction of total phosphorus, ranging from 335 to 738 mg/kg. Simultaneously, the autogenetic calcium phosphorus (ACa-P) was the main fraction of inorganic phosphorus, ranging from 145.4 to 543.2 mg/kg. Vertical distribution of different phosphorus forms in different sediment cores was distinguishing, and most of them tended to increase toward the surface sediment, indicated that the phosphorus concentration was related to the humanity with a certain extent. The relationships between TP and occluded phosphorus and ACa-P were significant. Nitrogen in the sediment was composed mainly of organic nitrogen, accounting for grater than 80 % of TN. NO₃ ^?-N was the dominate fraction of inorganic nitrogen in the surface sediment, ranging between 51 and 346 mg/kg (151.1 ± 104.4 mg/kg), and accounting for between 2.2 and 17.7 % of total sediment nitrogen (6.2 ± 5.6 %). The ratio of organic carbon and TN in sediment was in range of 6.0–25.8 and presented a tendency of lake centre >lake sides, indicating that nitrogen accumulated in the sediments from lake sides came mainly from terrestrial source and nitrogen was mainly autogenetic in lake centre. Ratio of N:P in all sampling sites was below 14, indicated that N was the limiting nutrient for algal growth in this lake.     

The distribution of nitrogen speciation and sources of nitrate in the north of Taihu Lake

Meiliang Bay and Gonghu Bay, in the north of Taihu Lake, are important water sources for the city of Wuxi, and increased eutrophication now threatens the safety of drinking water. The distribution of nitrogen (N) speciation and source of N in the surface waters in the north of Taihu Lake is studied, which was an important first step in controlling N pollution. The result shows that the average concentration of ammonia (NH₄ ⁺) and nitrate (NO₃ ^?) of surface water in Meiliang Bay was 0.32 and 0.35 mg/L, while 0.21 and 0.74 mg/L of Gonghu Bay, in which both bays had serious nitrate pollution. The concentrations of NH₄ ⁺ and NO₃ ^? in the surface water of the two bays had a trend of gradual decrease from north to south. The maximum concentrations of NH₄ ⁺ and NO₃ ^? of two bays were observed near the inflowing rivers, and the maximum concentrations of NH₄ ⁺ in surface water of two bays were 0.49 and 0.61, and 0.77 and 1.38 mg/L of NO₃ ^?. The concentration of NH₄ ⁺ in the interstitial water of the two bays had a trend of gradual decrease from west to east, but NO₃ ^? had the opposite tendency. The maximum concentrations of NH₄ ⁺ in the interstitial water of the two bays were 5.88 and 4.64, and 3.58 and 7.18 mg/L of NO₃ ^?. The exchangeable NH₄ ⁺ content in the sediment of Meiliang Bay had a trend of gradual decrease from north to south, but Gonghu Bay showed the reverse. The exchangeable NO₃ ^? content in the sediment of Meiliang Bay had a trend of gradual decrease from east to west, but a decreasing trend from north to south was observed in Gonghu Bay. The maximum concentrations of exchangeable NH₄ ⁺ were determined, and the values were 96.25 and 74.90 mg/kg, as well as NO₃ ^? with the values of 12.06 and 7.08 mg/kg. Chemical fertilizer and domestic sewage were the major sources of nitrate in surface water of Gonghu Bay, contributing 39.16 and 47.79%, respectively. Domestic sewage was the major source of nitrate in Meiliang Bay, contributing 84.79%. The denitrification process in Gonghu Bay was more apparent than in Meiliang Bay. Mixing and dilution processes had important effects on changing the concentration of nitrate transportation in the two bays.     

A poly-ε-caprolactone based biofilm carrier for nitrate removal from water

Nitrate removal from water has been accomplished by heterotrophic biofilms using organic carbon as a source of reducing power. To overcome the natural limitation in organic carbon in water, a poly-ε-caprolactone based biofilm carrier that serves simultaneously as a biofilm carrier and as a source of organic carbon was developed and tested in the present work. The feasibility of the new biofilm carrier for nitrate removal from water was evaluated in a packed bed reactor. The combination of size and structure provided a carrier element having high surface area and void volume, 1,170 m²/m³ and 67 %, respectively. A maximum denitrification rate of 4.4 mg N–NO₃ ^?/(L.h) (9.2 mg N–NO₃ ^?/(m².h)) was achieved in the packed bed reactor at 20 °C and pH 7.0. Main advantages of the biofilm carrier developed in the present work are its mechanical stability in water even after biofilm formation and controlled release of organic carbon by enzymatic reactions. The proposed biotechnology to remove nitrate from groundwater is robust and easy to operate.     

Effect of rising atmospheric CO2 on sediment and water 15N interactions in experimental riparian wetland

The experiment was conducted to ascertain net production and consumption rates of ¹⁵NH₄ ⁺ and ¹⁵NO₃ ^? for water and sediment in a wetland. This was done using ¹⁵N isotope pool dilution methodology under ambient and elevated atmospheric CO₂ concentrations in experimental riparian wetlands to obtain the gross N transformation rates. The ¹⁵N budget for sediment was also estimated. The results suggested that the differences in high proportion of ¹⁵N concentration in the overlying water body under elevated CO₂ could be attributed to the low production and high consumption rates of ¹⁵NH₄ ⁺ in sediment. The elevated CO₂ effect on production and consumption of NH₄ ⁺ decreased by 144 % (P = 0.014) and increased by 153 % (P = 0.009), respectively. Thereby, ¹⁵NH₄ ⁺ production rates are negatively related with ¹⁵NO₃ ^? consumption rates and this accounted for the decreases in net ¹⁵NO₃ ^? consumption under CO₂ enrichment in the wetland sediment by 11 % (P = 0.528). Therefore, ¹⁵NO₃ ^? production and consumption rates may strongly depend on NH₄ ⁺ production. Inorganic ¹⁵N and total ¹⁵N exported from sediment to overlying water body by the effect of CO₂ were 41 % (P = 0.071) and 18 % (P = 0.000), respectively. Therefore, low net ¹⁵NH₄ ⁺ production and high ¹⁵NH₄ ⁺ consumption rates under elevated CO₂ may partly explain the significant reduction of N from the sediment.     

Geochemical,isotopic and hydrological mass balance approaches to constrain the lake water–groundwater interaction in Dal Lake,Kashmir Valley

It is important to have qualitative as well as quantitative understanding of the hydraulic exchange between lake and groundwater for effective water resource management. Dal, a famous urban fresh water lake, plays a fundamental role in social, cultural and economic dynamics of the Kashmir Valley. In this paper geochemical, isotopic and hydrological mass balance approaches are used to constrain the lake water–groundwater interaction of Dal Lake and to identify the sources of lake water. Water samples of precipitation (n = 27), lake water (n = 18) and groundwater (n = 32) were collected across the lake and its catchment for the analysis of δ¹⁸O and δ²H. A total of 444 lake water samples and 440 groundwater samples (springs, tube wells and dug wells) were collected for the analysis of Ca²⁺, Mg²⁺, HCO₃ ^?, SO₄ ^2?, Cl^?, NO₃ ^?, Na⁺ and K⁺. Water table and lake water level were monitored at 40 observation locations in the catchment. Water table map including pH and EC values corroborate and verify the gaining nature of the Dal Lake. Stable isotopes of lake water in Boddal and Gagribal basins showed more deviation from the global meteoric water line than Hazratbal and Nigeen basins, indicating the evaporation of lake water. The isotopic and geochemical mass balance suggested that groundwater contributes a significant proportion (23–40%) to Dal Lake. The estimated average groundwater contribution to Dal Lake ranged from 31.2 × 10³ to 674 × 10³ m³ day^?1 with an average of 276 × 10³ m³ day^?1. The study will be useful to delineate the possible sources of nutrients and pollutants entering the lake and for the management of lake water resources for sustainable development.     

Sources and Processes Affecting Nitrate in a Dam-Controlled Subtropical River,Southwest China

Excess nutrient (N and P) loads are recognized as the major cause of serious water quality problems in China. River systems play a very important role in nitrate (NO₃ ^?) transportation and transformation in the aquatic environment. To understand and clarify the sources and processes affecting NO₃ ^? in river basins, we have examined spatial and temporal variations of concentration and dual-isotopic composition of NO₃ ^? in the dam-controlled Jialing River, a major tributary of the Yangtze River where land use is dominated by agriculture. Water samples were collected in July 2008 and February 2009 from the main channel of the Jialing River and its major tributaries. The δ¹⁵N and δ¹⁸O of NO₃ ^? range from 1.5 to 11.0 ‰ (average 6.2 ‰) and ?5.0 to 11.1 ‰ (average, 1.6 ‰), respectively. NO₃ ^? isotope data and δ¹⁸O of water interpreted in combination with hydrological and chemical data suggest that most of the NO₃ ^? input is from nitrification during the rainy season, and discharge of sewage and manure in the upper course and from cities accounts for much of the NO₃ ^? load during the dry season. The construction of cascade dams has led to retention of Si and a decrease in the Si/N ratio, implying that assimilation and/or denitrification may significantly affect NO₃ ^? in the dam area, as demonstrated by NO₃ ^? and dissolved Si concentrations, and \(\updelta^{ 1 5} {\text{N}}_{{{\text{NO}}_{3} }}\) and \(\updelta^{ 1 8} {\text{O}}_{{{\text{NO}}_{3} }}\) values. This study indicates that dual-isotopic data can be used to identify NO₃ ^? pollution sources and the processes NO₃ ^? has undergone during its retention and transport in the watershed of the dam-controlled Jialing River.     

Geochemical evaluation of nitrate and fluoride contamination in varied hydrogeological environs of Prakasam district,southern India

Hydrogeochemical controlling factors for high rate of groundwater contamination in stressed aquifer of fractured, consolidated rocks belonging to semi-arid watershed are examined. The groundwater in mid-eastern part of Prakasam district confining to Musi-Gundlakamma sub-basins is heavily contaminated with nitrate and fluoride. Distinct water chemistry is noticed among each group of samples segregated based on concentration of these contaminants. The nitrate is as high as 594 mg/l and 57 % of the samples have it in toxic level as per BIS drinking water standards, so also the fluoride which has reached a maximum of 8.96 mq/l and 43 % of samples are not fit for human consumption. Nitrate contamination is high in shallow aquifers and granitic terrains, whereas fluoride is in excess concentration in deeper zones and meta-sediments among the tested wells, and 25 % of samples suffer from both NO₃ ^? and F^? contamination. Na⁺ among cations and HCO₃ ^? among anions are the dominant species followed by Mg²⁺ and Cl^?. The NO₃ ^?-rich groundwater is of Ca²⁺–Mg²⁺–HCO₃ ^?, Ca²⁺–Mg²⁺–Cl^? and Na⁺–HCO₃ ^? type. The F^?-rich groundwater is dominantly of Na⁺–HCO₃ ^? type and few are of Na⁺–SO₄ ^2? type, whereas the safe waters (without any contaminants) are of Ca²⁺–Mg²⁺–HCO₃ ^?– and Na⁺–HCO₃ ^? types. High molecular percentage of Na⁺, Cl^?, SO₄ ^2? and K^? in NO₃ ^? rich groundwater indicates simultaneous contribution of many elements through domestic sewerage and agriculture activity. It is further confirmed by analogous ratios of commonly associated ions viz NO₃ ^?:Cl^?:SO₄ ^2? and NO₃ ^?:K⁺:Cl^? which are 22:56:22 and 42:10:48, respectively. The F^? rich groundwater is unique by having higher content of Na⁺ (183 %) and HCO₃ ^? (28 %) than safe waters. The K⁺:F^?:Ca²⁺ ratio of 10:5:85 and K⁺:F^?: SO₄ ^2? of 16:7:77 support lithological origin of F^? facilitated by precipitation of CaCO₃ which removes Ca²⁺ from solution. The high concentrations of Na⁺, CO₃ ^? and HCO₃ ^? in these waters act as catalyst allowing more fluorite to dissolve into the groundwater. The indices, ratios and scatter plots indicate that the NO₃ ^? rich groundwater has evolved through silicate weathering-anthropogenic activity-evapotranspiration processes, whereas F^? rich groundwater attained its unique chemistry from mineral dissolution-water–rock interaction-ion exchange. Both the waters are subjected to external infusion of certain elements such as Na⁺, Cl^?, NO₃ ^? which are further aggravated by evaporation processes leading to heavy accumulation of contaminants by raising the water density. Presence of NO₃ ^? rich samples within F^? rich groundwater Group and vice versa authenticates the proposed evolution processes.     

Oyster (<Emphasis Type="Italic">Crassostrea virginica</Emphasis>) Aquaculture Shifts Sediment Nitrogen Processes toward Mineralization over Denitrification

Filter-feeding bivalves, like oysters, couple pelagic primary production with benthic microbial processes by consuming plankton from the water column and depositing unassimilated material on sediment. Conceptual models suggest that at low to moderate oyster densities, this deposition can stimulate benthic denitrification by providing denitrifying bacteria with organic carbon and nitrogen (N). While enhanced denitrification has been found at oyster reefs, data from oyster aquaculture are limited and equivocal. This study measured seasonal rates of denitrification, as well as dissimilatory nitrate reduction to ammonium (DNRA), and dissolved inorganic N fluxes at a rack and bag eastern oyster (Crassostrea virginica) aquaculture farm. Consistent with models, denitrification was enhanced within the farm, with an average annual increase of 350% compared to a reference site. However, absolute denitrification rates were low relative to other coastal systems, reaching a maximum of 19.2 μmol m^?2 h^?1. Denitrification appeared to be nitrate (NO₃ ^?) limited, likely due to inhibited nitrification caused by sediment anoxia. Denitrification may also have been limited by competition for NO₃ ^? with DNRA, which accounted for an average of 76% of NO₃ ^? reduction. Consequently, direct release of ammonium (NH₄ ⁺) from mineralization to the water column was the most significant benthic N pathway, with seasonal rates exceeding 900 μmol m^?2 h^?1 within the farm. The enhanced N processes were spatially limited however, with significantly higher rates directly under oysters, compared to in between oyster racks. For commercial aquaculture farms like this, with moderate oyster densities (100–200 oysters m^?2), denitrification may be enhanced, but nonetheless limited by biodeposition-induced sediment anoxia. The resulting shift in the sediment N balance toward processes that regenerate reactive N to the water column rather than remove N is an important consideration for water quality.     

Impacts of a large Sahelian city on groundwater hydrodynamics and quality: example of Niamey (Niger)

The management of groundwater resources is very important in the semiarid Sahel region, which is experiencing rapid urban development. Impacts of urbanization on groundwater resources were investigated in the unconfined aquifer of the Continental Terminal beneath the city of Niamey, Niger, using water level and chemical data. Hydrodynamic and chemical changes are best described by a combination of factors including the historical development of the city, current land use, water-table depth and topography. Seasonal groundwater recharge occurs with high spatial variability, as indicated by water-level monitoring in all wells, but there was no interannual trend over the 5-year study period. Groundwater salinity shows high spatial variability and a minor rising trend. The highest salinity is in the old city centre, with Na–NO₃ dominant, and it increases seasonally with recharge. Salinity is much lower and more variable in the suburbs (Ca–HCO₃, Ca–NO₃, and Na–NO₃ dominant). Nitrate is the main ionic contaminant and is seasonally or permanently above the international guidelines for drinking water quality in 36 % of sampled wells, with a peak value of 112 mg L^?1 NO₃–N (8 meq L^?1). Comparison of urban and rural sites indicates a long-term increase in groundwater recharge and nitrate enrichment in the urban area with serious implications for groundwater management in the region.     

Nutrient dynamics in pore water of tidal marshes near the Yangtze Estuary and Hangzhou Bay, China

Tidal marshes act as a buffer system for nutrients in the pore water and play important roles in controlling the budget of nutrients and pollutants that reach the sea. Spatial and seasonal dynamics of pore water nutrients were surveyed in three tidal marshes (Chongming Island, Hengsha Island, and Fengxian tidal flat) near the Yangtze Estuary and Hangzhou Bay from August 2007 to May 2008. Nutrient variations in pore water closely followed seawater quality in the estuaries, while the average concentration of NH₄ ⁺–N, the main form of inorganic nitrogen in pore water, was over two orders of magnitude higher than that in seawater which was dominated by nitrate. NH₄ ⁺–N export (13.81 μmol m^?2 h^?1) was lower than the import of (NO₃ ^?+NO₂ ^?)–N (?24.17 μmol m^?2 h^?1) into sediment over the 1-year period, hence reducing N-eutrophication in coastal waters. The export of SiO₃ ^2?–Si and PO₄ ^3?–P from tidal marshes regulated nutrient level and composition and lifted the ratio beyond potentidal element limitation in the coastal system. Moreover, macrophyte plants (Spartina alterniflora and Phragmites australis) played significant roles in controlling nutrient concentration in pore water and its exchange between marshes and estuaries. Fengxian marsh was characterized by higher nutrient concentrations and fluxes than other marshes in response to the more serious eutrophication in Hangzhou Bay than in the Yangtze Estuary.     

<Emphasis Type="Italic">Inoculum</Emphasis>-free start-up of biofilm- and sludge-based deammonification systems in pilot scale

Undiluted reject water from the dewatering of anaerobic sludge with an average total nitrogen content of 718 ± 117 mg L^?1 (n = 63) was used to start-up autotrophic nitrogen removal in three different pilot-scale (3 m³) deammonification configurations: (1) biofilm; (2) activated sludge sequence batch; and (3) two-staged (nitritation–anammox). Time- and concentration-based aeration control with alternating aerobic/anaerobic phases was applied for all reactor configurations. All reactors were initiated without anammox-specific inoculum, and biofilm was grown onto blank carriers. During the initial start-up period, biological nitrogen removal was found to be inhibited by an excessive free ammonia content (>10 mg-N L^?1), resulting from the use of high-strength reject water as the process feed. After implementation of free ammonia control by pH adjustment to 6.5–7.5, propagation of the deammonification process was observed with increased nitrogen removal with slight accumulation of NO₃ ^?–N. The highest total nitrogen removal rates were achieved with the single-reactor biofilm- and sludge-based deammonification processes (1.04 and 0.30 kg-N m^?3 day^?1, respectively). The critical factors for successful start-up and stable operation of deammonification reactors turned out to be control of pH below 7.5, dissolved oxygen at 0.3–0.8 mg-O₂ L^?1 and influent solids values below 1000 nephelometric turbidity units. Microbial analysis demonstrated that highest anammox enrichment was achieved in the biofilm reactor (9.40 × 10⁸ copies g^?1 total suspended solids). These data demonstrate the potential of an in-situ grown sludge- or biofilm-based concept for the development and propagation of deammonification process.     

Evaluation of groundwater quality and health risks from contamination in the north edge of the Loess Plateau,Yulin City,Northwest China

Groundwater is a vital source for domestic and irrigation purposes in the loess area of Northwest China where climate is arid. However, the quality of groundwater in this area is deteriorating due to intensive industrial and agricultural activities, and this has a great adverse impact on human health. In order to better understand the pollution status of groundwater and the health risks to local residents, comprehensive water quality index was applied to assess the quality of drinking water in Yulin City, Northwest China, and sodium adsorption ratio, sodium percentage, residual sodium carbonate and permeability index were used to evaluate the quality of irrigation water. Moreover, the health risks caused by ingestion of groundwater were evaluated using the model proposed by the Ministry of Environmental Protection of the PR China. The results show that all groundwater samples for irrigation will not induce soil salinization, but more than half of them are not suitable for drinking, and Fe, Mn, TH, Mg²⁺ and NO₃–N are the common contaminants which are mainly from natural processes, industrial and agricultural activities. The health risk assessment indicates that children face greater non-carcinogenic risk than adults. The order of contribution of contaminants to non-carcinogenic risk is NO₃ ^? > As > F^? > Fe > Mn > Ba²⁺ > Cr⁶⁺ > Zn > NO₂ ^?. The average carcinogenic risk of carcinogens (Cr⁶⁺ and As) is 1.17 × 10^?4 and 1.37 × 10^?4 for adults and children, respectively, which surpasses the permissible level (1 × 10^?6) stipulated by the Ministry of Environmental Protection of the PR China. Hence, effective measures are highly demanded to manage groundwater pollution and reduce the risks to human health.     

Variability of groundwater nitrate concentrations over time in arid basin aquifers: sources, mechanisms of transport, and implications for conceptual models

In groundwater of the Trans-Pecos region of West Texas, unexpectedly high levels of nitrate (NO₃ ^?) are documented in four basins: Red Light Draw, Eagle Flats, Wild Horse and Michigan Flats, and Lobo and Ryan Flats. NO₃ ^? concentrations are changing over time in the majority (82.8 %) of wells and are increasing in most (69.8 %). The temporal change raises questions about the potential sources of NO₃ ^? and about flow dynamics in these basins. Presence of NO₃ ^? and temporal variability in concentration has implications beyond contamination risk because it indicates relatively rapid recharge (<60 years) to the basin groundwaters which was not expected based on previous estimates from chloride mass balance models and groundwater age-dating techniques. This research combines existing data ranging back to the 1940s with data collected in 2011 to document a multi-decadal trend of overall increasing NO₃ ^? concentration in deep basin groundwaters. Chlorofluorocarbon analyses of groundwater collected during 2011 indicate the presence of young (<70 years) water in the basins. The authors infer from these data that there are mechanism(s) by which relatively rapid and widespread recharge occurs on the basin floors; that recharge is spatially and temporally variable and that it results from both anthropogenic (irrigated agriculture) and natural (precipitation) sources. In light of these observations, fundamental conceptual models of flow in these basins should be re-evaluated.     

Drinking quality assessment of some groundwater sources along the stretch of Jhelum River in Kashmir Himalaya

The physicochemical properties and major ion chemistry of the groundwater sources from alluvial aquifers along the stretch (60 km) of Jhelum River in Kashmir Himalaya were determined in order to identify hydro-geochemical processes and their suitability for drinking purposes. The data depicted that calcium and bicarbonates were dominating among the cations and anions. The results indicate the trend of cation dominance as Ca²⁺ > Na⁺ > Mg²⁺ > K⁺, whereas anion dominance was in the order of HCO₃ ^? > Cl^? > SO₄ ^2?. Ratio of calcium to magnesium indicated the dissolution of Ca²⁺ from CaCO₃, which results in an increased levels of Ca²⁺ in the groundwater. Interpretation of Piper Trilinear plot understands the various geochemical processes affecting the groundwater quality and shows groundwater was dominated by Ca–HCO₃ type. The pH was recorded in the slightly alkalinity range 7.2–7.8 and was showing positive correlation with HCO₃ ^?. The chloro-alkaline indices revealed 86% of the sources exchange by a type of base-exchange reactions, rest by cation–anion exchange. Gibbs diagram revealed groundwater sources fall in the category of rock dominance. The concentration of the nitrogen compounds was in the progression of NO₃–N > NH₄–N > NO₂–N, and the PO₄ ^? fluctuated from 0.12 to 0.22 mg/L. Moreover, corrosivity ratio indicated that water from the majority of sources (71%) is safe to supply using pipes without any corrosive effects, while 29% of sources are corrosive in nature and need non-corrosive pipes for transporting and lifting of groundwater. The results revealed, groundwater samples were within permissible limits as prescribed by International and National standards, for drinking purposes. The State government and NGO’s can show their interest in utilizing such water resources to overcome the shortage of drinking water in a sustainable way for the daily consumption of the people living in the vicinity of Jhelum River.     

Assessment of groundwater quality in and around Vedaraniyam,South India

Groundwater from 47 wells were analyzed on the basis of hydrochemical parameters like pH, electric conductivity, total dissolved solids, Ca²⁺, Mg²⁺, Na⁺, K⁺, Cl^?, CO₃ ^2?, HCO₃ ^?, NO₃ ^?, PO₄ ^3? and F^? in the Cauvery delta of Vedaraniyam coast. Further, water quality index (WQI), sodium percentage (Na %), sodium absorption ratio, residual sodium carbonate, permeability index and Kelley’s ratio were evaluated to understand the suitability of water for drinking and irrigation purposes. The result shows significant difference in the quality of water along the coastal stretch. The order of dominance of major ions is as follows: Na⁺ ≥ Mg²⁺ ≥ Ca²⁺ ≥ K⁺ and Cl^? ≥ HCO₃ ^? ≥ CO₃ ^2? ≥ PO₄ ^3? ≥ F^?. Na/Cl, Cl/HCO₃ ratio and Revelle index confirmed that 60–70 % of the samples were affected by saline water intrusion. WQI showed that 36 % of the samples were good for drinking and the remaining were poor and unsuitable for drinking purpose. The degradation of groundwater quality was found to be mainly due to over-exploitation, brackish aquaculture practice, fertilizer input from agriculture and also due to domestic sewage.     

Aerosol-trace gases interactions and their role in air quality control of Delhi city (India)

Atmospheric dust is considered to be the major cause of poor air quality due to its contribution to high particulate levels, but their interaction with the acidic gases helps in controlling the level of SO₂ and NO₂ through ambient neutralization reactions. In the present study, the interaction of acidic gases such as SO₂ and NO₂ with alkaline dust was investigated during October, 2013–July, 2014 at a site named as Babarpur located at the Trans-Yamuna region of Delhi. The concentration of SO₂ ranged from 10 to 170 μg/m³ with an average of 36 μg/m³ while that of NO₂ ranged from 15 to 54 μg/m³ with an average of 26?±?8 μg/m³. The results were observed to be well within the National Ambient Air Quality Standard (NAAQS) limits prescribed by the Central Pollution Control Board (CPCB). The average concentrations of SO₂ during day and night time were recorded as 31?±?18 and 43?±?53 μg/m³ respectively while the mean concentrations of NO₂ during day and night time were recorded as 26?±?7 and 27?±?12 μg/m³ respectively. A positive correlation between SO₄^2? and NO₃^? was also observed indicating their secondary aerosol formation. In aerosol phase, average concentrations of SO₄^2? during day and night time were 3.9?±?0.3 and 6.5?±?2.3 μg/m³ respectively while that of NO₃^? were 9.5?±?1.5 and 7.3?±?0.5 μg/m³ respectively. Molar ratios of Ca²⁺/SO₄^2?, NH₄⁺/SO₄^2?, and NH₄⁺/NO₃^? were observed as 8, 5, and 1.7 during daytime and 1.5, 0.4, and 0.8 during nighttime respectively. Such molar ratios confirmed high concentrations of sulphate (SO₄)^2? and low concentrations of nitrate (NO₃^?) during night time, thereby indicating different pathway of aerosol formation during day and night time. Surface morphology and elemental composition of aerosol samples showed various oval, globular, and platy shapes where the diameter varied from few nm to ~5 μm depending on their precursors. There were certain shapes like grossularite, irregular aggregate, grape-like, triangular, and flattened which indicate the crustal origin of aerosols and their possible role in SO₂ and NO₂ adsorption.