Dissolved and particulate trace metals and their partitioning in a hypoxic estuary: The Tanshui Estuary in Northern Taiwan

The distribution and partitioning of trace metals (Co, Cu, Fe, Mn, Ni, and Zn) between dissolved and particulate phases were studied in the Tanshui Estuary. The upper reach of the estuary is hypoxic and heavily polluted due to domestic and industrial discharges. The concentration ranges of dissolved and leachable particulate trace metals in the Tanshui Estuary were: Co: 0.3–6.1 nM, 1.8–18.6 mg kg⁻¹; Cu: 5–53 nM, 22–500 mg kg⁻¹; Fe: 388–3,364 nM, 1.08–6.67%; Mn: 57–2,914 nM, 209–1,169 mg kg⁻¹; Ni: 7–310 nM, 6–108 mg kg⁻¹; and Zn: 12–176 nM, 62–1,316 mg kg⁻¹; respectively. The dissolved concentrations of the metals were 2–35 times higher than the average values of the world river water. The distributions of dissolved and particulate studied metals, except Mn, in the estuary showed scattering, which could be attributed to the discharges from many industrial wastewater disposal works located in the upper tributaries. The daily input of dissolved metals from the disposal works to the Tanshui Estuary ranged from 0.1–0.4 tons. Dissolved Mn was nearly conservative in the region with salinity higher than 10 psu, while particulate Mn decreased in the region with salinity of 10–15 psu. The concentration increased significantly seawards, corresponding with the distribution of dissolved oxygen. The distribution coefficient (K_D) for Mn in the lower estuary was nearly three orders of magnitude higher than in the upper estuary. This phenomenon may be attributed to the diffusion of Mn from the anoxic sediment in the upper estuary and gradual oxidation into particulate Mn in the middle and lower estuary as the estuarine water became more oxygenated. The distribution coefficient for Cu decreased with increasing salinity. The percentages of trace metals bound by suspended particulate matter decreased in the following order: Fe>Zn, Cu>Co>Mn>Ni.     

Flocculation Potential of Estuarine Particles: The Importance of Environmental Factors and of the Spatial and Seasonal Variability of Suspended Particulate Matter

Estuarine systems are complex environments where seasonal and spatial variations occur in concentrations of suspended particulate matter, in primary constituents, and in organic matter content. This study investigated in the laboratory the flocculation potential of estuarine-suspended particulate matter throughout the year in order to better identify the controlling factors and their hierarchy. Kinetic experiments were performed in the lab with a “video in lab” device, based on a jar test technique, using suspended sediments sampled every 2 months over a 14-month period at three stations in the Seine estuary (France). These sampling stations are representative of (1) the upper estuary, dominated by freshwater, and (2) the middle estuary, characterized by a strong salinity gradient and the presence of an estuarine turbidity maximum. Experiments were performed at a constant low turbulent shear stress characteristic of slack water periods (i.e., a Kolmogorov microscale >1,000 μm). Flocculation processes were estimated using three parameters: flocculation efficiency, flocculation speed, and flocculation time. Results showed that the flocculation that occurred at the three stations was mainly influenced by the concentration of the suspended particulate matter: maximum floc size was observed for concentrations above 0.1 g l⁻¹ while no flocculation was observed for concentrations below 0.004 g l⁻¹. Diatom blooms strongly enhanced flocculation speed and, to a lesser extent, flocculation efficiency. During this period, the maximum flocculation speed of 6 μm min⁻¹ corresponded to a flocculation time of less than 20 min. Salinity did not appear to automatically enhance flocculation, which depended on the constituents of suspended sediments and on the content and concentration of organic matter. Examination of the variability of 2D fractal dimension during flocculation experiments revealed restructuring of flocs during aggregation. This was observed as a rapid decrease in the floc fractal dimension from 2 to 1.4 during the first minutes of the flocculation stage, followed by a slight increase up to 1.8. Deflocculation experiments enabled determination of the influence of turbulent structures on flocculation processes and confirmed that turbulent intensity is one of the main determining factors of maximum floc size.     

Short-term water quality variability in two tropical estuaries,central Sumatra

We examined high frequency fluctuations in water quality parameters in two tropical coastal plain estuaries in response to changing tidal flow conditions. The variability in total suspended sediments (TSS), volatile suspended solids (VSS), total organic carbon (TOC) concentrations, and indicators of water quality, including pH, temperature, salinity, and dissolved oxygen, over one spring tidal cycle during the early wet monsoon season was measured in two estuaries in eastern Sumatra. The relatively high rainfall experienced throughout the year, in combination with the recent extensive vegetation clearing and modification of the landscape, resulted in significant concentrations of TSS, VSS, and TOC being discharged to coastal waters. Maximum values are reached on the ebb tide (TSS > 1,013 mg l⁻¹; VSS > 800 mg l⁻¹; TOC >60 mg l⁻¹). The influence of freshwater discharge and tidal flow on water properties of the lower estuaries is also marked by the variability in salinity, dissolved oxygen, and pH over the tidal cycle, with minimum values for each of these parameters following maximum current velocities and after the completion of the strong ebb tide. Estimation of seaward sediment fluxes, which are of significant interest in a region where rapid environmental change is occurring, would require further examination of sedimentary processes, such as resuspension and advection of sediment, as well as a consideration of neap-spring tidal variations and the effect of seasonality on estuarine circulation.     

Spatiotemporal changes in cadmium contamination in the Seine estuary (France)

Cadmium (Cd) is among the major contaminants in the Seine estuary. In the biota, the RNO (Réseau National d’Observation, the French Mussel-Watch) has shown that Cd concentrations in mussels living at the mouth of the estuary are related to changes in inputs to this area of phosphogypsum, a calcium sulphate that is a by-product of the phosphoric acid naturally enriched with Cd. In the water column, Cd concentrations at several key estuary sites show a very marked trend toward decreased contamination in the particles as well as in the dissolved phase. The behavior of Cd in the estuary has been studied between 1991 and 1998 in the framework of the scientific program Seine-Aval. This program has highlighted punctual Cd inputs in the estuarine water column. The partition of Cd between the dissolved and the particulate phase, previously described in various estuaries, is characterized by an intense phenomenon of solubilization in the mixing zone freshwater-seawater, but the colloidal Cd fraction remains low along the whole salinity gradient, about 5% to 10% of the apparent dissolved fraction. Although the decrease of inputs induced a fall of Cd concentrations in the water column, laboratory experiments show that the estuarine particles are far from being exhausted in Cd. Despite continuous efforts to reduce the urban and industrial inputs into the estuarine and coastal waters, the Seine estuary still remains very contaminated by Cd.     

Dissolved aluminum in four Chinese estuaries: evidence of biogeochemical uncoupling of Al with nutrients

Four Chinese estuaries, the Jiaojiang, Luanhe, Shuangtaizihe, and Yalujiang were investigated to determine Al geochemistry and inter-relations between Al and nutrients. These estuaries are characterised by low particulate organic carbon and high turbidity, with various tidal regimes. Dissolved Al was determined by fluorescence method after liquid–liquid extraction into n-hexanol. Concentrations of Al in the Luanhe estuary are relatively high (1.5–2.0 μM) and approximately uniform over the salinity range sampled, suggesting the influence of in situ sources/processes. In the Shuangtaizihe estuary, riverine concentrations of Al (1.8–2.2 μM) decrease with higher chlorinity, indicating the predominance of simple dilution by seawater. The Jiaojiang and Yalujiang provide evidence that Al is removed from water column at early stages of estuarine mixing, owing to probably the particle–solution reactions (e.g. flocculation) in the estuary. The Al data are further compared with total suspended matter and nutrients in these estuaries. The data sets indicate that aluminum is not dominantly coupled to the cycle of nutrients.     

Importance of CDOM Distribution and Photoreactivity in a Shallow Texas Estuary

This study examined freshwater discharge of dissolved organic matter (DOM) to the shallow Lavaca–Matagorda (LM) Bay estuarine system along the central Texas coast and investigated whether chromophoric DOM (CDOM) photochemical reactions have the potential to stimulate microbial activity within LM estuarine waters. Dissolved organic carbon (DOC) concentrations ranged from 3 to 10 mg C l⁻¹ and CDOM levels (reported as a ₃₀₅) ranged from 8 to 77 m⁻¹ during April and July, 2007, when the LM system was experiencing very high freshwater inputs. DOC and CDOM levels were well-correlated with salinities > 3, but exhibited considerable variability at salinities < 3. CDOM photobleaching rates (i.e., decrease in a ₃₀₅ resulting from exposure to solar radiation) for estuarine samples ranged from 0.014 to 0.021 h⁻¹, corresponding to photobleaching half-lives of 33–50 h. Our data indicate when Matagorda Bay waters photobleach; dissolved organic carbon utilization is enhanced perhaps due to enhanced microbial respiration of biologically labile photoproducts (BLPs). Net ecosystem metabolism calculations indicate that most of the LM system was net heterotrophic during our study. We estimate that BLP formation could support up to 20% of the daily microbial respiratory C demand in LM surface waters and combined with direct photochemical oxygen consumption could have an important influence on O₂ cycles in the LM system.     

Modeling on adsorption–desorption of trace metals to suspended particle matter in the Changjiang Estuary

The uptake and release of trace metals (Cu, Ni, Zn, Cd, and Co) in estuaries are studied using river and sea end-member waters and suspended particulate matter (SPM) collected from the Changjiang Estuary, China. The kinetics of adsorption and desorption were studied in terms of environmental factors (pH, SPM loading, and salinity) and metal concentrations. The uptake of the metals studied onto SPM occurred mostly within 10 h and reached an asymptotic value within 40 h in the Changjiang Estuary. As low pH river water flows into the high pH seawater and the water become more alkaline as it approaches to the seaside of estuary, metals adsorb more on SPM in higher pH water, thus, particulate phase transport of metal become increasingly important in the seaward side of the estuary. The percentage of adsorption recovery and the distribution coefficients for trace metals remained to be relatively invariable and a significant reduction only occurred in very high concentrations of metals (>0.1 mg L⁻¹). The general effect of salinity on metal behavior was to decrease the degree of adsorption of Cu, Zn, Cd, Co, and Ni onto SPM but to increase their adsorption equilibrium pH. The adsorption–desorption kinetics of trace metals were further investigated using Kurbatov adsorption model. The model appears to be most useful for the metals showing the conservative behavior during mixing of river and seawater in the estuary. Our work demonstrates that dissolved concentration of trace metals in estuary can be modeled based on the metal concentration in SPM, pH and salinity using a Kurbatov adsorption model assuming the natural SPM as a simple surfaced molecule.     

The transport of Osmium and Strontium isotopes through a tropical estuary

We have determined the concentration and isotopic composition of Os and Sr in the estuarine waters from the Godavari delta in Peninsular India. Additionally, we have obtained the concentration and isotopic composition of Os and Al concentration in selected suspended particulate matter recovered on 0.45 μm filters. The Na, K, Mg, and Ca concentrations of water samples obtained along salinity gradients from two distributary channels in the delta display a general two component mixing between river- and sea-water. The data also reveal that Al behaves non-conservatively and is affected by interactions with suspended particulates. The ⁸⁷Sr/⁸⁶Sr ratio of the riverine end member is 0.716303 and shows a linear decrease with salinity to seawater value and Sr isotope systematics indicate that its behavior is conservative in the estuary.The ¹⁸⁷Os/¹⁸⁸Os ratio of the Godavari river end-member is 1.24 and within error of the average eroding upper continental crust. The concentration and isotopic composition of Os through the two salinity transects shows that its behavior in the Godavari estuary is complex and non-conservative. By comparing the Al/Os ratios and Os isotopes in the waters with those of the suspended particulate we find that both Os gains and losses occur in the water column. However, in one of the distributaries (Vasishta) the Os concentration of suspended load increases and that of dissolved load decreases with increasing salinity towards the Bay of Bengal end-member. We infer that there is removal of seawater Os at higher salinities. The estimated mean residence time of Os in the oceans is 37 ± 14 (2σ) kyr. A comparison of the Os concentration of the Bay of Bengal and the Indian Ocean waters indicates that the rainout rate of Os in Bay of Bengal is 30% faster than that in the open ocean and suggests that the observed discrepancy between the mean residence time calculated from mass balance considerations and that estimated from the relaxation of the Os isotopic ratio in marine record may not be real as the relaxation time experiments likely estimate the residence time for a basin/sub-basin and not for the entire ocean.     

Satellite Estimates of Wide-Range Suspended Sediment Concentrations in Changjiang (Yangtze) Estuary Using MERIS Data

The Changjiang (Yangtze) estuarine and coastal waters are characterized by suspended sediments over a wide range of concentrations from 20 to 2,500 mg l⁻¹. Suspended sediment plays important roles in the estuarine and coastal system and environment. Previous algorithms for satellite estimates of suspended sediment concentration (SSC) showed a great limitation in that only low to moderate concentrations (up to 50 mg l⁻¹) could be reliably estimated. In this study, we developed a semi-empirical radiative transfer (SERT) model with physically based empirical coefficients to estimate SSC from MERIS data over turbid waters with a much wider range of SSC. The model was based on the Kubelka–Munk two-stream approximation of radiative transfer theory and calibrated using datasets from in situ measurements and outdoor controlled tank experiments. The results show that the sensitivity and saturation level of remote-sensing reflectance to SSC are dependent on wavelengths and SSC levels. Therefore, the SERT model, coupled with a multi-conditional algorithm scheme adapted to satellite retrieval of wide-range SSC, was proposed. Results suggest that this method is more effective and accurate in the estimation of SSC over turbid waters.     

Sorption Model for Dissolved Aluminium in Freshwaters

A series of aluminium speciation measurements were madein the freshwaters of the Yare and Great Ouse rivers (England). Samples were analysedfor dissolved and particulate Al, suspended particulate matter (SPM), and other alliedchemical species in order to assess the role of sorption processes on the suspended phasesin controlling dissolved Al levels. Partitioning of Al occurs between solid andsolution phases with a distribution coefficient (K_d) which varies over about one anda half orders of magnitude for suspended particle concentrations of comparablemagnitude. A sorption model is proposed for dissolved Al concentrations in thesefreshwaters with most of the data fitting the model defined by a zone with K_dvalues of 0.316 × 10⁶ and 10⁷. However, a few data points lie outside thiszone, suggesting that other processes may also influence dissolved Al distributions.Nevertheless, the model may serve as a starting point for predicting concentrations ofdissolved Al in rivers where SPM levels are moderate to high (>1 mg l^-1 but< 75 mg l^-1), and indeed, this model works reasonably well for the Conway system(Wales). Further, the empirical distribution coefficient, K_d, decreases withincreasing suspended particle concentration, which may be due in part to colloidal phenomena.     

Seasonal distributions of suspended particulate material and dissolved nutrients in a coastal plain estuary

The temporal and spatial distributions of salinity, dissolved oxygen, suspended particulate material (SPM), and dissolved nutrients were determined during 1983 in the Choptank River, an estuarine tributary of Chesapeake Bay. During winter and spring freshets, the middle estuary was strongly stratified with changes in salinity of up to 5‰ occurring over 1 m depth intervals. Periodically, the lower estuary was stratified due to the intrusion of higher salinity water from the main channel of Chesapeake Bay. During summer this intrusion caused minimum oxygen and maximum NH₄ ⁺ concentrations at the mouth of the Choptank River estuary. Highest concentrations of SPM, particulate carbon (PC), particulate nitrogen (PN), total nitrogen (TN), total phosphorous (TP) and dissolved inorganic nitrogen (DIN) occurred in the upper estuary during the early spring freshet. In contrast, minimum soluble reactive phosphate (SRP) concentrations were highest in the upper estuary in summer when freshwater discharge was low. In spring, PC:PN ratios were >13, indicating a strong influence by allochthonous plant detritus on PC and PN concentrations. However, high concentrations of PC and PN in fall coincided with maximum chlorophyll a concentrations and PC:PN ratios were <8, indicating in situ productivity controlled PC and PN levels. During late spring and summer, DIN concentrations decreased from >100 to <10 μg-at l^?1, resulting mainly from the nonconservative behavior of NO₃ ^?, which dominated the DIN pool. Atomic ratios of both the inorganic and total forms of N and P exceeded 100 in spring, but by summer, ratios decreased to <5 and <15, respectively. The seasonal and spatial changes in both absolute concentrations and ratios of N and P reflect the strong influence of allochthonous inputs on nutrient distributions in spring, followed by the effects of internal processes in summer and fall.     

Plankton and dissolved inorganic carbon isotopic composition in a river-dominated estuary: Apalachicola Bay, Florida

To characterize the isotopic composition of organisms at the base of the food web and the controls on their variability, the concentration and δ¹³C isotopic composition of dissolved inorganic carbon (DIC) and plankton δ¹³C, δ¹⁵N, and δ³⁴S were measured. The measurements were made during periods of high and low river flow in Apalachicola Bay, Florida, United States, over 3 yr. DIC concentration and δ¹³C values were related to salinity, indicating that conservative mixing of riverine and marine waters was responsible for the overall distributions. The usefulness of DIC δ^13C data for characterizing the trophic processes within the estuary was dependent upon the residence time of water within the season. Plankton δ¹³C values varied from −22‰ to −30‰ and were directly related to estuarine DIC δ¹³C, offset by a factor of roughly −20‰. This offset factor varied with salinity. Values of δ³⁴S in estuarine plankton (station means ranged from 11.4‰ to 13.1‰) were depleted relative to marine plankton (17.7±0.4‰) possibly due to the admixture of³⁴S-depleted sedimentary sulfide with estuarine samples. Values of δ³⁴S in plankton were not related to δ¹³C values of plankton and were only weakly correlated to the salinity of the water from which the plankton were collected, indicating that marine sulfate was the primary source of planktonic sulfur. Values of δ¹⁵N in plankton varied from 5.5‰ to 10.7‰ and appeared related to dominance of the sample by phytoplankton or zooplankton. Estuarine plankton was¹⁵N enriched relative to offshore plankton and estuarine sediment.     

Aluminum in the macrotidal Yalujiang estuary: Partitioning of Al along the estuarine gradients and flux

Water samples were collected from the Yalujiang estuary in both flood periods (August 1992 and August 1994) and dry season (May 1996) and were analyzed for aluminum (Al). Al behaves non-conservatively in the Yalujiang estuary, and a significant loss (70–80%) in dissolved concentration is observed in the upper estuary, in spite of seasonal variation in water discharge and sediment load. About 0.4×10⁶, tons of Al is annually transported from Yalujiang to the estuary, of which the particulate pool clearly dominates. The particulate Al flux through the Yalujiang contributes 35% of the total Al input from Chinese rivers to the Yellow Sea. The data sets from size fractionation and C-18 SPE separation demonstrate that a large fraction of dissolved Al is in colloidal (≈50%) and organically complex (≈60%) forms in the Yalujiang. The observed scavenging from solution to particulate pools in the estuary is most likely through the flocculation of colloidal and organic-complexed Al, which results in a considerable change in dissolved-particulate partitioning, shown by laboratory mixing experiments. Exchange between dissolved and particulate phases is examined by analysis of K_d, the distribution coefficient. The empirical relationship of K_d with chlorinity and suspended matter concentrations was investigated with field observations and model simulations. The model indicated that K_d values of Al are inversely related to the amount of total suspended matter, but K_d-chlorinity plots show different features between dry and flood seasons.     

Aquatic hydrocarbon distributions in the Seine estuary: Biogenic polyaromatics and n-alkanes

Dissolved and particulate hydrocarbons of biogenic origin were investigated for the first time in surface waters along the Seine River and its estuary. They comprise n-alkanes (n-ALKs) and diagenetic polycyclic aromatic hydrocarbons (PAHs). Samples were collected in three different sections of the estuary: the riverine zone, the mixing zone, and the marine zone. At the river mouth, two mooring stations were used for the collection of samples over tidal cycles. Total particulate n-ALK concentrations ranged from 31 ng 1^?1 to 2,918 ng 1^?1, or 5 μg g^?1 dry ng 1^?1, or 2 μg g^?1 of SM. Concentrations varied with the SM load and could be related to sedimentation and estuarine mixing. The sources of the n-ALKs were different in each zone of the estuary. The dissolved n-ALKs displayed lower concentrations than the particulate phase, varying from 136 ng 1^?1 to 344 ng 1^?1, while biogenic dissolved PAHs were almost absent.     

Transparent Exopolymer Particles (TEP) in a River-Dominated Estuary: Spatial–Temporal Distributions and an Assessment of Controls upon TEP Formation

Transparent exopolymer particle (TEP) distributions were examined in North Carolina’s Neuse River Estuary (NRE) over a 1-year period, and experiments were conducted to examine controls upon TEP formation. TEP-carbon averaged 16% of the total organic carbon pool in the NRE. From May to early August 2007, TEP ranged from 805 to 1,801 μg xanthan gum (XG) L⁻¹. A large phytoplankton bloom peaked in early August and then subsequently declined. Within 2 weeks of the bloom’s peak, TEP concentrations increased to >3,500 μg XG L⁻¹ and remained elevated through mid-December. Decreasing water temperatures and enhanced retention due to drought conditions in Fall 2007 likely aided in the persistence of TEP concentrations during this timeframe. Thereafter, TEP decreased coincident with increased river flow and flushing of the estuary that began in January 2008, and TEP remained low (ranging from 991 to 1,712 μg XG L⁻¹) until the end of April 2008. TEP was positively correlated with salinity, suggesting that cation availability (which co-varies with salinity and stabilizes the structural integrity of TEP) may play a role in estuarine TEP formation. In two cation addition experiments using water from the mesohaline region, TEP concentrations tended to be higher in treatments with vs. without cations added. Statistically significant relationships were also found between in situ TEP concentrations and pH, mixing, and temperature, suggesting that a complex suite of environmental parameters affect TEP formation and its distribution in estuaries.     

An Idealized Model and Systematic Process Study of Oxygen Depletion in Highly Turbid Estuaries

The sensitivity of oxygen depletion in turbid estuaries to parameters like freshwater discharge, depth, and sediment availability is investigated using an idealized model. The model describes tidally averaged circulation and suspended sediment concentration (SSC), which are input into an advection–diffusion sink module of dissolved oxygen (DO). Based on the analysis of field data collected in the Ems estuary, the modeled oxygen depletion rates are proportional to SSC. The model is calibrated to the observed variation of DO with SSC and temperature. Modeled DO closely tracks changes to the estuarine turbidity zone (ETZ): increased channel depth, decreased freshwater discharge, and decreased mixing move the ETZ upstream, amplify SSCs, and decrease DO. Summertime temperatures produce lower DO than cooler periods. Model results are consistent with historical measurements in the Ems, which indicate that hypoxic events (DO concentrations < 2 mg l⁻¹) have occurred more frequently after deepening from 5 to 7 m.     

Distribution of carbon in a tropical hypersaline estuary,the Casamance (Senegal,West Africa)

The Casamance estuary, on the coast of Senegal, is an inverse hypersaline estuary: salinity increases landward, and dry season salinity values are up to 172 psu due to the evaporation of seawater. Dissolved inorganic carbon (DIC) concentrations decreased landward as a negative linear function of salinity. Thermodynamic modelling and the absence of CaCO₃ in the sediments indicate that this loss of DIC was not due to calcite precipitation in the main water body. The innermost, almost landlocked, waters contained high phytoplankton biomass (50–300 μg chl I^?1) and high concentrations of allochthonous dissolved organic carbon. Photosynthetic uptake of DIC and subsequent particulate organic carbon sedimentation is proposed as hypothetical explanation of the relationship between DIC and salinity; localized overheating in shallow waters might also be involved.     

Interaction of acid mine drainage with waters and sediments at the Corona stream, Lousal mine (Iberian Pyrite Belt, Southern Portugal)

This study investigates the geochemical characteristics of the acid mine drainage discharged from the abandoned mine adits and tailing piles in the vicinity of the Lousal mine and evaluates the extent of pollution on water and on the stream sediments of the Corona stream. Atmospheric precipitation interacting with sulphide minerals in exposed tailings produces runoff water with pH values as low as 1.9–2.9 and high concentrations of (9,249–20,700 mg l⁻¹), Fe (959–4,830 mg l⁻¹) and Al (136–624 mg l⁻¹). The acidic effluents and mixed stream water carry elevated Cu, Pb, Zn, Cd and As concentrations that exceed the water quality standards. However, the severity of contamination generally decreases 4 km downstream of the source due to mixing with fresh waters, which causes the dilution of dissolved toxic metals and neutralization of acidity. Some natural attenuation of the contaminants also occurs due to the general reduced solubility of most trace metals, which may be removed from solution, by either co-precipitation or adsorption to the iron and aluminium precipitates.     

An SF<Subscript>6</Subscript> Tracer Study of the Flow Dynamics in the Stockton Deep Water Ship Channel: Implications for Dissolved Oxygen Dynamics

A sulfur hexafluoride (SF₆) tracer release experiment was conducted in the Stockton Deep Water Ship Channel (DWSC) to quantify mixing and transport rates. SF₆ was injected in the San Joaquin River upstream of the DWSC and mapped for 8 days. From the temporal change in SF₆ distributions, the longitudinal dispersion coefficient (K _x ) was determined to be 32.7 ± 3.6 m² s⁻¹ and the net velocity was 1.75 ± 0.03 km day⁻¹. Based on the decrease in SF₆ inventory during the experiment, the pulsed residence time for waters in the DWSC was estimated at ∼17 days. Within the DWSC from Stockton downstream to Turner Cut, dissolved oxygen concentrations maintained a steady state value of 4 mg l⁻¹. These values are below water quality objectives for the time of year. The low flow rates observed in the DWSC and the inability of oxygen-rich waters from downstream to mix into the DWSC upstream of Turner Cut contribute to the low dissolved oxygen concentration.     

Fluoride,nitrate and water hardness in groundwater supplied to the rural communities of Ensenada County,Baja California,Mexico

The hydrogeochemistry of 26 wells belonging to ten different aquifers in the county of Ensenada, Baja California, is studied. These wells are all used to supply the rural communities in the region, which comprise ~37,000 inhabitants, excluding the city of Ensenada. High total dissolved solids (TDS) concentrations (maximum 7.35 g l⁻¹) indicate that salt is a ubiquitous contaminant in the aquifers due to seawater intrusion. The aquifers that support extensive agriculture activities (Maneadero, San Quintín, San Simón and El Rosario) are characterized by higher N–NO₃ concentrations (maximum 20 mg l⁻¹) derived from fertilizers. Fluoride concentrations exceed the 1.5 mg l⁻¹ Mexican official limit in only four wells. The enrichments of F⁻ in the southern aquifers are thought to be associated to water–rock interactions controlled mainly by Na–Ca equilibrium reactions with fluorite, as suggested from high dissolved Na concentrations in these waters. In the northern aquifer of Maneadero, no enrichment of Na is found and a geothermal source for F⁻ is likely. Water is hard to moderately hard, with Ca/Mg ratios >1. Although drinking water directly from the tap is not a common practice in these localities, most sources have concentrations of major ions and TDS that exceed the Mexican official limits.