Measuring dissolved organic carbon δ13C in freshwaters using total organic carbon cavity ring-down spectroscopy (TOC-CRDS)

This article reports the first application of coupled total organic carbon cavity ring-down spectroscopy (TOC-CRDS) for the analysis of the ??¹³C signature of dissolved organic carbon (DOC) in freshwater samples. DOC represents a major, dynamic component of the global carbon cycle. The export of DOC from soils into rivers and groundwaters may be highly climate sensitive, and much of this export may occur in ephemeral fluxes. Thus, a robust, simple and inexpensive method for the continuous determination of DOC concentration and quality is urgently needed. We detail recent advances made in the analysis of the ??¹³C signature of DOC using a TOC-CRDS system optimised for the analysis of DOC with natural abundances greater than 2.5?mg?L^?1 with no sample pre-concentration required and sample volumes of 40?mL. Precision between replicated samples was comparable to conventional analysis by gas-source isotope ratio mass spectrometry, yielding ??¹³C values with standard deviations of?±?0.5??? for DOC concentrations higher than 1.5?mg?L^?1. The utility of this technique for the analysis of DOC in samples with a broad range of compositions and concentrations (2.5?C25?mg?L^?1 DOC) is demonstrated. Since DOC ??¹³C can be measured continuously, ca. 45?min per measurement, this method enables the online monitoring of DOC in river water, water intakes and treated waters, allowing changes in DOC fluxes to be monitored in real time.     

Seasonal variations of organic-carbon and nutrient transport through a tropical estuary (Tsengwen) in southwestern Taiwan

This paper reports the fluvial fluxes and estuarine transport of organic carbon and nutrients from a tropical river (Tsengwen River), southwestern Taiwan. Riverine fluxes of organic carbon and nutrients were highly variable temporally, due primarily to temporal variations in river discharge and suspended load. The sediment yield of the drainage basin during the study period (1995–1996, 616 tonne km^–2 year^–1) was ca. 15 times lower than that of the long-term (1960–1998) average (9379 tonne km² year^–1), resulting mainly from the damming effect and historically low record of river water discharge (5.02 m³ s^–1) in 1995. The flushing time of river water in the estuary varied from 5 months in the dry season to >4.5 days in the wet season and about 1 day in the flood period. Consequently, distributions of nutrients, dissolved organic carbon (DOC) and particulate organic carbon (POC) were of highly seasonal variability in the estuary. Nutrients and POC behaved nonconservatively but DOC behaved conservatively in the estuary. DOC fluxes were generally greater than POC fluxes with the exception that POC fluxes considerably exceeded DOC fluxes during the flood period. Degradation of DOC and POC within the span of flushing time was insignificant and may contribute little amount of CO₂ to the estuary during the wet season and flood period. Net estuarine fluxes of nutrients were determined by riverine fluxes and estuarine removals (or additions) of nutrients. The magnitude of estuarine removal or addition for a nutrient was also seasonally variable, and these processes must be considered for net flux estimates from the river to the sea. As a result, nonconservative fluxes of dissolved inorganic phosphorus (DIP) from the estuary are –0.002, –0.09 and –0.59 mmol m^–2 day^–1, respectively, for dry season, wet season and flood period, indicating internal sinks of DIP during all seasons. Due to high turbidity and short flushing time of estuarine water, DIP in the flood period may be derived largely from geochemical processes rather than biological removal, and this DIP should not be included in an annual estimate of carbon budget. The internal sink of phosphorus corresponds to a net organic carbon production (photosynthesis–respiration, p–r) during dry (0.21 mmol m^–2 day^–1) and wet (9.5 mmol m^–2 day^–1) seasons. The magnitude of net production (p–r) is 1.5 mol m^–2 year^–1, indicating that the estuary is autotrophic in 1995. However, there is a net nitrogen loss (nitrogen fixation–denitrification < 0) in 1995, but the magnitude is small (–0.17 mol m^–2 year^–1).     

Reassessment of the Ocean-To-Atmosphere Flux of Carbon Monoxide

Abstract

Carbon monoxide (CO) in the surface sea waters is produced predominantly by photochemical processes, oxidized by micro-organisms and outgassed to the atmosphere. to assess carbon monoxide flux from the oceans to the atmosphere, the photochemical production and microbial oxidation of carbon monoxide in the oceanic mixed-layer was investigated during several oeanographic cruises and in the laboratory. the photoproduction rate of carbon monoxide was found to be well correlated to the concentration of dissolved organic carbon (DOC) in coastal and open ocean surface waters. Taking a global average carbon monoxide production rate of 10 ± 2 nmole litre^?1 (mg DOC hr)^?1 in the surface open ocean water, and 25 ± 7 nmole litre^?1 (mg DOC hr)^?1 in coastal sea water, at cloud-free summer solar noon, the photochemical production of carbon monoxide in the global oceans is estimated to be at a rate of 1200 ± 200 Tg CO y^?1. the microbial carbon monoxide turnover time in the mixed-layer was observed to range from hours in a coastal estuary to 16 days in the Pacific along 1057deg; W in dark incubations. Natural sunlight can largely inhibit the microbial consumption of carbon monoxide in surface water. On a global scale, microbial consumption is responsible for the loss of less than 10% of photochemical produced carbon monoxide in the surface ocean. Field measurements have shown that the net transport of carbon monoxide from the euphotic zone to the underlying deeper ocean water is limited and that the overall life time in surface sea waters is less than 3-4 hours. When combined, these field measurements with the photoproduction and microbial consumption rates obtained, we estimate the oceanic flux to the atmosphere is about 1000 ± 200 Tg CO y^?1, which represents the largest single source of atmospheric carbon monoxide.     

Release of dissolved organic carbon (DOC) by the scyphozoan jellyfish Aurelia aurita and its potential influence on the production of planktic bacteria

A series of incubation experiments were made to measure the rate of release of dissolved organic carbon (DOC) by the jellyfish Aurelia aurita (L.) (collected in 1991–1992 in Gullmarsfjorden, Sweden). Release of DOC by medusae (9.5 to 18 cm in diameter) from the Skagerrak ranged from 0.70 to 1.6 mg C ind^-1 d^-1 with a mean of 1.2 mg C ind^-1 d^-1 (SD=0.29 mg C ind^-1 d^-1, n=10). Based on data from the literature for two medusa populations, this can be equivalent to 2.5 and 7.1% of the carbon assimilated in one season (June to September). This was similar to the amount of carbon allocated to reproduction. Bacterial abundance was monitored to evaluate the possible stimulating effect of the DOC released. Bacterial growth was stimulated by the presence of A. aurita. The importance of A. aurita as a source of DOC on a large scale is small compared to exudate from primary producers. The volume surrounding each medusa, wherein the DOC released may be enough to sustain a bacterial production such as the one reported from the Swedish west coast, is equivalent to a sphere with a diameter of 0.5 m. Thus, considering the patchy distribution of medusae, the local influence of their DOC release could be important.     

Phytoplankton exudate release as an energy source for the growth of pelagic bacteria

The release of dissolved organic carbon (DOC) from phytolankton during photosynthesis, and the utilization of this carbon by planktonic bacteria, was studied using ¹⁴CO₂ and selective filtration. Natural sea water samples from a coastal area of the Northern Baltic Sea were incubated in the laboratory for detailed studies, and in situ for estimation of annual dynamics. In a laboratory incubation (at +1°C) the concentration of ¹⁴C-labelled dissolved organic carbon increased for about 2 h and then reached a steady state, representing about 0. 1% of the total DOC. Labelled organic carbon in the phytoplankton and bacterial fractions continued to increase almost linearly. The continuous increase in the bacterial fraction is thought to represent almost instantaneous utilization of the DOC released from the phytoplankton during photosynthesis. As an annual average, in 4 h in situ incubations, about 65% of the labelled organic carbon was found in the phytoplankton fraction (>3 m), about 27% in the bacterial fraction (0.2 to 3 m) and the remaining 8% as DOC (<0.2 m). Large variations in these percentages were recorded. The measured annual primary production was 93 g C m^-2 (March to December), and the estimated bacterial production due to phytoplankton exudates 29 g C m^-2. This represents a release of DOC of about 45% of the corrected annual primary production of 110 g C m^-2 (assuming a bacterial growth efficiency of 0.6).     

Effects of rising temperature on pelagic biogeochemistry in mesocosm systems: a comparative analysis of the AQUASHIFT Kiel experiments

A comparative analysis of data, obtained during four indoor-mesocosm experiments with natural spring plankton communities from the Baltic Sea, was conducted to investigate whether biogeochemical cycling is affected by an increase in water temperature of up to 6?°C above present-day conditions. In all experiments, warming stimulated in particular heterotrophic bacterial processes and had an accelerating effect on the temporal development of phytoplankton blooms. This was also mirrored in the build-up and partitioning of organic matter between particulate and dissolved phases. Thus, warming increased both the magnitude and rate of dissolved organic carbon (DOC) build-up, whereas the accumulation of particulate organic carbon (POC) and phosphorus (POP) decreased with rising temperature. In concert, the observed temperature-mediated changes in biogeochemical components suggest strong shifts in the functioning of marine pelagic food webs and the ocean’s biological carbon pump, hence providing potential feedback mechanisms to Earth’s climate system.     

Reagenzienfreie Bestimmung von Quecksilberspuren in Wasserproben

A comprehensive ecological monitoring of hazardous substances is indispensable to preserve our health and environment. Therefore, fast and inexpensive techniques for routine analysis of pollutants are essential. However, in the measuring procedure itself often toxic reagents are used producing hazardous waste. Omitting environmentally hazardous substances in the analysis procedure is an important contribution to a more sustainable and green analytical chemistry. A reagent-free method for ultra-trace (pg to ng?L^-1) mercury determination in water samples was developed and validated. An active nanogold collector integrated in a fully automated flow injection system is the core of this new method. All mercury species dissolved in the water sample are adsorbed and preconcentrated on the nano-structured gold surface of the collector. After rinsing and drying of the collector, the enriched mercury is thermally desorbed and finally measured by atomic fluorescence spectrometry. This method was optimized and validated for the determination of mercury in natural waters. The influence of various water constituents was investigated and only high contents of dissolved organic carbon (DOC) showed interferences of mercury preconcentration due to the strong complexation of mercury by DOC. This restriction can be solved by UV-irradiation, i.?e. reagent-free digestion of DOC rich samples prior to the preconcentration procedure. Mercury concentration of several natural river and sea waters and water from the discharge of a waste water treatment plant were determined with this new analytical method. Accuracy and precision of the method were demonstrated by several recovery experiments in natural water samples (recoveries: 96–102?%) and by analysis of the certified reference material BCR-579 (Mercury in Coastal Sea Water; recovery: 101?±?1?%). With a detection limit of only 80?pg?Hg?L^–1 the proposed method is highly sensitive. Furthermore the method avoids potential contamination of the sample by reagent addition and is due to the reagent-free procedure environment-friendly. Hence this work is an important contribution to sustainable environmental analysis and at the same time improves accurate routine mercury trace analysis.     

Release of dissolved organic carbon from the estuarine intertidal macroalga Enteromorpha prolifera

The estuarine macroalga Enteromorpha prolifera was collected from Coos Bay, Oregon, USA during 1981, and its release of photosynthate as dissolved organic carbon (DOC) was studied using ¹⁴C as a tracer. During photosynthesis in 30 S sea water, with a fixation rate averaging 7.37 mg C g^-1 dry wt h^-1, release ranged from 0.13 to 0.57 mg C g^-1 dry wt h^-1 and from 1.65 to 6.23% of total fixed carbon. Release of DOC appears to be linear with time over 3 h. As exposed algae become increasingly desiccated, their photosynthetic rates decline dramatically, but upon reimmersion the highly desiccated algae lose a larger fraction of their fixed carbon than the slightly desiccated algae. This loss comes in a pulse release of DOC over the initial 15 min, followed by declining release rates. The pulse loss due to rainfall is 5 times greater than that due to tidal resubmergence, and may briefly exceed the prior photosynthetic rate. Although lowering the salinity from 30 to 5 does not substantially alter photosynthetic rates, it does increase the DOC release range up to 1.02 mg C g^-1 dry wt h^-1 and 16.10% of fixed carbon. Heterotrophic microbes from the algal habitat readily use the available DOC at about 15% h^-1.     

Fluxes and Transport of Organic Carbon and Trace Metals in the Tropical Tsengwen Estuary,Southwestern Taiwan

Distributions of organic carbon and trace metals were investigated in the tropical Tsengwen river end-member and in the estuary to better understand thoroughly the riverine fluxes and estuarine transports of constituents into the sea. Experimental results indicated that riverine fluxes of organic carbon and trace metals possessed a highly temporal variability, attributed primarily to temporal variation in river water discharge and suspended load. More than 70% of annual fluxes of dissolved constituents and >90% of particulate constituents arose from river floods caused by summer typhoons. the flushing time of fresh water in the estuary varied from a half month in the dry season to a half day in the flood period. Dissolved organic carbon (DOC) and nutrienttype metals (Cd, Cu, Zn) were conservatively transported through the estuary. Dissolved particle-reactive metals (Mn, Pb), however, were apparently transported non-conservatively through the estuary. Particulate organic carbon (POC) and trace metals (PTM) were transported non-conservatively by following the transport mode of total suspended matter (TSM) in the estuary. DOC slightly dominates the transport of organic carbon while particle-reactive PTM predominates the transport of trace metals through the estuary. Total organic carbon (TOC) in estuarine sediment was progressively enriched with ¹³C downstream, as derived by mixing the overlying TSM between terrestrial and marine end-members. Distributions of trace metals in sediment were subsequently controlled by sedimentary TOC and particle size. Based on results presented here, we believe that enrichments of trace metals in the estuary are attributed primarily to the natural processes of transport and sedimentation of fluvial TSM     

Influences of Suspended Particles on the Runoff of Pesticides from an Agricultural Field at Askim, SE-Norway

Field and laboratory experiments were conducted to study the loss of particles from agricultural fields, and the role of suspended particles in carrying pesticides in surface runoff and drainage water. Propiconazole, a widely used fungicide was applied to experimental fields located at Askim, SE-Norway. Samples from surface runoff and drainage water were collected and analyzed for sediment mass, pesticides, particulate and dissolved organic carbon through a whole year. The surface soil and the runoff material were characterized by its particle size distribution, organic carbon content in size fractions and its ability to bind propiconazole. The results show that (1) particle runoff mostly occurred during the rainfall event shortly after harrowing in autumn. The highest particle concentration observed in the surface runoff water was 4600 mg l^–1, and in the drainage water 1130 mg l^–1; (2) the erosion of surface soil is size selective. The runoff sediment contained finer particle/aggregates rich in organic matter compared to its original surface soil; (3) the distribution coefficient (K _d) of propiconazole was significantly higher in the runoff sediment than in the parent soil. According to our calculation, particle-bound propiconazole can represent up to 23% of the total amount of propiconazole in a water sample with a sediment concentration of 7600 mg l^–1, which will significantly influence the transport behavior of the pesticide.     

Reassessment of the Ocean-To-Atmosphere Flux of Carbon Monoxide

Carbon monoxide (CO) in the surface sea waters is produced predominantly by photochemical processes, oxidized by micro-organisms and outgassed to the atmosphere. to assess carbon monoxide flux from the oceans to the atmosphere, the photochemical production and microbial oxidation of carbon monoxide in the oceanic mixed-layer was investigated during several oeanographic cruises and in the laboratory. the photoproduction rate of carbon monoxide was found to be well correlated to the concentration of dissolved organic carbon (DOC) in coastal and open ocean surface waters. Taking a global average carbon monoxide production rate of 10 ± 2 nmole litre^-1 (mg DOC hr)^-1 in the surface open ocean water, and 25 ± 7 nmole litre^-1 (mg DOC hr)^-1 in coastal sea water, at cloud-free summer solar noon, the photochemical production of carbon monoxide in the global oceans is estimated to be at a rate of 1200 ± 200 Tg CO y^-1. the microbial carbon monoxide turnover time in the mixed-layer was observed to range from hours in a coastal estuary to 16 days in the Pacific along 1057deg; W in dark incubations. Natural sunlight can largely inhibit the microbial consumption of carbon monoxide in surface water. On a global scale, microbial consumption is responsible for the loss of less than 10% of photochemical produced carbon monoxide in the surface ocean. Field measurements have shown that the net transport of carbon monoxide from the euphotic zone to the underlying deeper ocean water is limited and that the overall life time in surface sea waters is less than 3-4 hours. When combined, these field measurements with the photoproduction and microbial consumption rates obtained, we estimate the oceanic flux to the atmosphere is about 1000 ± 200 Tg CO y^-1, which represents the largest single source of atmospheric carbon monoxide.     

Spatial variations in the N2O emissions and denitrification potential of riparian buffer strips in a contaminated urban river

Spatial variations in the N₂O emissions and denitrification potential of riparian buffer strips (RBS) in a polluted river were examined. The river received large pollutant inputs from urban runoff and wastewater discharge, resulting in impaired water quality in the river and downstream reservoir. The potential for nitrogen removal by RBS was evaluated by measuring in situ N₂O emission fluxes in static closed chambers and sediment denitrification potentials with acetylene inhibition techniques. The results showed that N₂O emission fluxes decreased from the upstream (16.39 μg/(m²·h)) to downstream (0.30 μg/(m²·h)) sites and from the water body to upland sites. The trend in decreasing N₂O emission fluxes in the downstream direction was mainly associated with sediment/soil textures (clay loam→sandy soil) and sediment/soil water contents and was also related to the vegetation along the RBS and nutrients in the sediments/soils. The correlation coefficient was highest (r=0.769) between the N₂O emission flux and sediment/soil water content. Sediment/soil denitrification potentials under N-amended and ambient conditions were higher (highest 32.86 mg/(kg·h)) for the upstream sites, which were consistent with in situ N₂O flux rates.     

Hydrographic and biological aspects of algal bloom in the Adriatic Sea in 1988

The interaction of hydrological, chemical and biological factors in a defined time may cause an excess bloom of phytoplankton in an ecosystem, which can persist over a long period or occur from time to time.

This phenomenon has been recorded from the northern Adriatic and coastal enclosed basins along the eastern Adriatic coast (Ka?tela Bay, Split) for a long time now.

During 1988 this phenomenon of increased production was recorded from almost the entire northern and middle Adriatic with some traces even in its southern part. Some preliminary results for that period point to the fact that this was caused very likely by exceptionally warm and dry weather, with no significant precipitations and wind. Such conditions affect horizontal and vertical stratification of water masses.

High photosynthetic radiation, increased quantities of alochthonous organic matter, either in the form of particulate or dissolved organic matter, either in the form of particulate or dissolved organic carbon (POC or DOC), influx of nutrients (via rivers, municipal sewage or upwelling) are the main causes of sudden bloom and rapid reproduction rate of phytoplankton species (Diatoms) to the large quantities to which the pollution of the entire coastal area is due.     

Effects of visible light radiation on macrophyte litter degradation and nutrient release in water samples from a eutrophic shallow lake

Visible light is a major fraction of the solar spectrum; however, information on visible light radiation of macrophyte detritus is lacking. In this study, we conducted a microcosm experiment to assess the effects of visible light radiation on degradation of two litter species: Potamogeton malaianus (P. malaianus) and Phragmites australis (Ph. australis). This research represents an investigation of mass loss, microbial activity and nutrients released over a period of 168 days. Overall, we found that visible light radiation had significant effects on litter decomposition, but it did not affect the microbial activities which degrade cellulose and lignin. The decomposition rate order of the three components in P. malaianus and Ph. australis in treatments was: cellulose?>?hemicellulose?>?lignin. The visible light radiation mainly affected the degradation of lignin, which is the primary compound in litter susceptible to photodegradation. The exposure to visible light radiation up to 17.6?Wm^?2 stimulated the dissolved organic carbon release and reduced the molecular weight to less reactive. Meanwhile, no obvious difference in nutrient contents (TP, TN, NO₃–N, NO₂–N, and NH₃–N) was observed among different visible light intensities. The results of this study contribute to better understanding of the photochemical behaviour of macrophyte litter in shallow lakes.     

Nutrients uptake and growth of Ulva lactuca (Linnaeus, 1753) in grey mullet (Mugil cephalus) wastewater versus natural estuarine water

This study investigates the capability of Ulva lactuca to grow in an integrated system, aiming to optimise the needing of resources and to decrease the ecological impact of wastewater. The nutrients uptake and the growth of U. lactuca in Mugil cephalus wastewater (WW) were evaluated and compared with U. lactuca cultivated in estuarine water (EW). Fresh thalli of U. lactuca were cultivated for 10 days in 5?L cylindrical tanks, 3 replicates per treatment. The uptake of dissolved inorganic nitrogen (DIN) and dissolved inorganic phosphorous (DIP), as well as the biomass yield and specific growth rate of U. lactuca, were assessed every two days. At the end of the experiment, U. lactuca resulted in a higher assimilation of DIN in EW (95.7?±?0.3%, mean?±?SE) than in wastewater (68.7?±?1.0%) (p?80%), as well as in the biomass yield and specific growth rate. This study demonstrates the efficiency of U. lactuca in the assimilation of DIN and DIP from M. cephalus WW, contributing to reduce the release of dissolved inorganic nutrients in the natural environment.     

Carbon sequestration in Taiwan harvested wood products

This study, with FAOSTAT and Taiwan data sources, estimates Taiwan carbon dioxide (CO₂) emissions in harvested wood products (HWP) by applying the three accounting methods suggested by the 2006 IPCC Guidelines. The investigation also explores impulse responses of CO₂ emissions to economic factors. Results from FAOSTAT and Taiwan data demonstrate an inconsistent production approach (PA) in the signs of the estimated CO₂ emissions. Average contributions of HWP from 1990 to 2008 for the stock change approach (SCA), PA and atmospheric flow approach (AFA) in Taiwan are ?3.195 Tg, 0.412 Tg and 10.632 Tg CO₂ emissions, respectively. SCA has determined the Taiwan HWP as a carbon reservoir; in contrast, PA and AFA have determined Taiwan HWP as a CO₂ emission. The net forest products imports into Taiwan induce the inconsistent signs of HWP carbon sequestration among SCA, PA and AFA. The vector autoregressive model (VAR) results also indicate that real GDP per capita is crucial for SCA CO₂ emissions, followed by exchange rate.     

Rate and extent of decomposition of dissolved organic matter in surface seawater

An experiment on the decomposition of the dissolved organic matter (DOM) in surface seawater was carried out under controlled laboratory conditions during a cruise of the R.V. Hakuho-Maru in the North-Equatorial Pacific (August/November, 1969). Surface seawater was placed in 300 ml oxygen bottles and incubated in the dark at 25°C. After selected time intervals, the dissolved organic-carbon (DOC) and the dissolved oxygen (DO) were determined for each bottle. The DOM in the surface seawater was described in terms of two labile fractions and a refractory one. The DOC decreased from 0.96 to 0.74 mgC/l during the first 50 days of incubation. Approximately 20% of the initial DOC (Fraction F_I) was oxidized. The other labile fraction, F_II was assumed to be 30 to 40% of the total DOM. The remaining half of the total DOM (Fraction F_III) is probably refractory and resistant to biochemical oxidation. The rate constant for decomposition was 0.0052 day^–1 for the total DOM and 0.033 day^–1 for F _I.     

A decade of investigations on groundwater arsenic contamination in Middle Ganga Plain,India

Groundwater arsenic (As) load in excess of drinking limit (50 µg L^?1) in the Gangetic Plains was first detected in 2002. Though the menace was known since about two decades from the downstream part of the plains in the Bengal Basin, comprising of Lower Ganga Plain and deltaic plains of Ganga–Brahmaputra–Meghna River system, little thought was given to its possible threat in the upstream parts in the Gangetic Plains beyond Garo-Rajmahal Hills. The contamination in Bengal Basin has become one of the extensively studied issues in the world and regarded as the severest case of health hazard in the history of mankind. The researches and investigations in the Gangetic Plains during the last decade (2003–2013) revealed that the eastern half of the plains, also referred as Middle Ganga Plain (MGP), is particularly affected by contamination, jeopardising the shallow aquifer-based drinking water supply. The present paper reviews researches and investigations carried out so far in MGP by various research institutes and government departments on wide array of issues of groundwater As such as its spatio-temporal variation, mobilisation paths, water level behaviour and flow regime, configuration of contaminated and safe aquifers and their recharge mechanism. Elevated conc. of groundwater As has been observed in grey and dark grey sediments of Holocene age (Newer Alluvium) deposited in a fluvio-lacustrine environment in the floodplain of the Ganga and most of its northern tributaries from Himalayas. Older Alluvium, comprising Pleistocene brownish yellow sediment, extending as deeper aquifers in Newer Alluvium areas, is low in groundwater As. Similarities and differences on issues between the MGP and the Bengal Basin have been discussed. The researches point towards the mobilisation process as reductive dissolution of iron hydroxide coating, rich in adsorbed As, mediated by microbial processes. The area is marked with shallow water level (<8.0 m below ground) with ample monsoonal recharge. The infiltrated rainwater and percolating water from surface water bodies carry organic carbon from sediments (particularly from the clay plugs in abandoned channels), abetting microbial processes, spread of anoxic front and release of As.     

N:P stoichiometry and transparent exopolymeric particles buffer ecological impacts of nutrients in the Ganga River: a mesocosm study

We investigated the possible drivers of the N:P stoichiometric shift and its relationship with micro-algal production of transparent exopolymeric particles (TEP) along a 35?km gradient of the Ganga River. The objective was to evaluate if the trade-off between N:P stoichiometry and production of TEP helps in maintaining water quality of the river. Mesocosm experiments were conducted to examine N:P-TEP linkages and its role in turbidity removal. In situ measurements did not show Si to be a limiting nutrient (N:Si?Aulacosira granulata and Fragilaria intermedia. Settling efficiency, turbidity removal and sedimentation of TEP, biogenic silica (BSi) and biomass all increased with decreasing N:P ratio proportionately to the amount of TEP produced in the mesocosm. The study demonstrates that trade-off between N:P stoichiometry and the production of TEP generates feedback to buffer the ecological impacts of nutrient pollution.     

Seasonal variations in physicochemical characteristics and cyanobacterial diversity of a lake in Northern India

Physicochemical analyses and cyanobacterial diversity of Ramgarh Lake water were performed at five sampling sites during winter, summer, and monsoon seasons. Higher load of solids, carbon, and nutrients were persistent throughout the analysis that indicates the conversion of lake from oligotrophic to eutrophic nature. High nutrients load enhanced cyanobacterial biomass, while low nutrients load produced relatively less biomass. The physicochemical parameters of water samples revealed minimum 2.9 mg L^?1 dissolved oxygen (DO) at site-1 during summer, while maximum (5.6 mg L^?1) at site-4 in monsoon season. Maximum biochemical oxygen demand (BOD) (40 mg L^?1) and chemical oxygen demand (COD) (126 mg L^?1) were recorded at site-1 during summer, whereas minimum BOD (18 mg L^?1) and COD (52 mg L^?1) were evident at site-3 in monsoon season. Minimum concentration of nitrate (0.72 mg L^?1) was recorded at site-3 in summer, whereas maximum 2.7 mg L^?1 was present at site-5 in winter season. The phosphate concentration was maximum (0.52 mg L^?1) at site-5 in summer, and minimum (0.18 mg L^?1) was observed at site-4 in monsoon season. Cyanobacterial diversity was higher during all the seasons, and dominated by the species of Microcystis at all the five sampling sites.