Estimation of dissolved inorganic nutrients fluxes from the Changjiang River into estuary

Because the estuary acts as either a trap or a source or both for nutrient elements and will modify greatly the riverine transport to the ocean, it is necessary to calculate the flux from river into estuary and that from estuary into sea, respectively. The present work aims to use a long-term record of nutrients concentrations and runoff discharges on H.e Datong section (625 km inland from the Changjiang River mouth) to identify the variability of nutrients concentrations and to estimate nutrients fluxes from the Changjiang River into the estuary.     

Estimation of dissolved inorganic nutrients fluxes from the Changjiang River into estuary

Because the estuary acts as either a trap or a source or both for nutrient elements and will modify greatly the riverine transport to the ocean, it is necessary to calculate the flux from river into estuary and that from estuary into sea, respectively. The present work aims to use a long-term record of nutrients concentrations and runoff discharges on H.e Datong section (625 km inland from the Changjiang River mouth) to identify the variability of nutrients concentrations and to estimate nutrients fluxes from the Changjiang River into the estuary.     

Methylated arsenic species in estuarine porewaters

Inorganic arsenic, monomethylarsenic and dimethylarsenic species have been observed in samples of sediment porewater collected from the Tamar Estuary in South-West England. Porewater samples were collected using in situ dialysis. The arsenic species were separated by hydride generation and concentrated by liquid nitrogen trapping, prior to analysis by directly coupled gas chromatography-atomic absorption spectroscopy. The predominant dissolved arsenic species present was inorganic arsenic (5-62 m?g dm^?3). However, this is the first time significant concentrations of methylated arsenic species have been quantified in estuarine porewaters (0.04–0.70 m?g dm^?3), accounting for between 1 and 4% of the total dissolved arsenic. The presence of methylated arsenic compounds in porewaters is attributed to in situ environmental methylation, although the possibility of methylated arsenic species being derived from biological debris cannot be excluded.     

Types of saltwater intrusion of the Changjiang Estuary

The Changjiang Estuary is characterized by multi-order bifurcations, unsteady submerged sandbars, mid-channel sandbars, creeks and riffles. The following four types of saltwater intrusion are found: (1) direct intrusion from the sea; (2) intrusion during tidal flooding; (3) intrusion from tidal flats overflow; and (4) salt water coming upstream through other waterways. These result in a complicated temporal and spatial salinity distribution. A high chlorinity concentration zone exists from the Liuhekou to the Sidongkou along the South Branch. The salinity during neap tide or ordinary tide is higher than during spring tide.     

Dissolved iron analysis in estuarine and coastal waters by using a modified adsorptive stripping chronopotentiometric (SCP) method

An electrochemical method based on adsorptive stripping chronopotentiometry (SCP) with a rotating mercury film electrode has been developed for the determination of dissolved iron (III) at subnanomolar concentrations in estuarine and coastal waters. The detection limit was 0.11 nM after adsorption time of 60 s. Compared to the other chronopotentiometric methods available for dissolved iron measurement in natural and estuarine waters, the procedure described here exhibits a 15-fold better sensitivity. Therefore, it allows one to accurately quantify concentrations commonly found in estuarine and coastal waters. Moreover, by using the speciation scheme proposed by Aldrich and van den Berg (Electroanalysis 10 (1998) 369), several forms could be measured, i.e. reactive iron (Fe R) and reactive iron (III) (Fe^III R), or estimated, i.e. complexed iron (Fe C) and reactive iron (II) (Fe^II R). The method described here is reliable, fast, inexpensive and compact. It was applied successfully to the study of the chemical speciation of dissolved iron along the salinity gradient of the Aulne estuary (Brittany-France).     

Types of saltwater intrusion of the Changjiang Estuary

The Changjiang Estuary is characterized by multi-order bifurcations, unsteady sub-merged sandbars, mid-channel sandbars, creeks and riffles. The following four types of saltwater intrusion are found: (1) direct intrusion from the sea; (2) intrusion during tidal flooding; (3) intrusion from tidal flats overflow; and (4) salt water coming upstream through other waterways. These result in a complicated temporal and spatial salinity distribution. A high chlorinity concentration zone exists from the Liuhekou to the Sidongkou along the South Branch. The salinity during neap tide or ordinary tide is higher than during spring tide.     

Neutral Lipid Content and Biomass Production in Skeletonema marinoi (Bacillariophyceae) Culture in Response to Nitrate Limitation

Microalgae are one of the most promising biodiesel feedstocks due to their efficiency in CO₂ fixation and high neutral lipid productivity. Nutrient–stress conditions, including nitrogen starvation, enhance neutral lipid content, but at the same time lead to a reduction of biomass. To maximize lipid production in the diatom Skeletonema marinoi, we investigated two different nitrogen starvation approaches. In the first experimental approach, inocula were effectuated in modified f/2 media with decreasing nitrogen concentration, while in the second experiment, nitrate concentration was gradually reduced through a collection/resuspension system in which the culture was periodically collected and resuspended in culture medium with a lower nitrate concentration. In the first approach, the neutral lipid accumulation was accompanied by a strong biomass reduction, as was expected, whereas the second experiment generated cultures with significantly higher neutral lipid content without affecting biomass production. The total proteins and total carbohydrates, which were also quantified in both experiments, suggest that in S. marinoi, neutral lipid accumulation during nutrient starvation did not derive from a new carbon partition of accumulated carbohydrates.     

Progress of estuarme research in China over last 50 years

It is well known that the estuarine research in China has got great achievements since the past 50 years. The development of estuarine research in China and progress in fundamental study are presented firstly in this paper. Especially in the aspect of theoretic studies, a distinctive feature is the combination studies of dynamics, sedimentology and geomorphology, which obtain a series of achievements, such as estuarine diluted water, estuarine fronts, turbidity maximum, sediment movement, formation of mouth bar, estuarine discontinuity phenomena, estuarine development, etc. Then some successful applications are introduced taking the Qiantang River Estuary and Yangtze Estuary as examples. Finally, main directions of estuarine research are discussed on fundamental study, the impacts of human activities on estuaries, estuarine material flux, sediment movement, prediction of estuarine erosion and accretion, estuarine discontinuity, artificial estuaries, land reclamation and wetland protection.     

Element geochemistry of Holocene sediment and paleoenvironmental change in the Changjiang Estuary

Analyses of 41 elements reveal that Holocene sediments In the Changjiang Estuary bear regular elemental compositions in different sedimentary environments, and Holocene sediments came mainly from the Changjiang River based on compositions of REEs and most trace elements. Some heavy metals are more enriched in the surface sediment than in the deltaic sediments, reflecting human impact. Elemental compositions of the river channel sediment are related to the influence of proximal sediments. Sedimentary environments exert some influences on elemental compositions. Some chemical indices can be used to record chemical weathering undergone by the Changjiang sediment and environmental change.     

Application of cold neutron prompt-gamma activation analysis in environmental studies of aquatic plants

This paper describes the use of cold-neutron prompt-gamma activation analysis (CNPGAA) to determine carbon, nitrogen, and phosphorus in the aquatic plant Typha domingensis, commonly known as cattail, during spring and fall seasons. According to studies of the Florida Everglades, cattail replaces sawgrass as a result of nutrient enrichment from farm water runoff. Nutrient enrichment, especially phosphorus, in sediment and the water column can lead to undesirable expansion. Early signs of this expansion are apparent in the Apalachicola River floodplain near Apalachicola, Florida, USA. This research project is designed to use cattails as biomonitors of nutrient enrichment in the lower Apalachicola River floodplain. Determination of carbon, nitrogen, and phosphorus in cattail using cold neutron prompt-gamma activation has been developed in our previous studies at the CNPGAA facility at the National Institute of Standards and Technology (NIST), USA. The results of numerous field samples, collected from the study area during spring and fall seasons in 2002, will be presented in this paper.     

Element geochemistry of Holocene sediment and paleoenvironmental change in the Changjiang Estuary

Analyses of 41 elements reveal that Holocene sediments in the Changjiang Estuary bear regular elemental compositions in different sedimentary environments, and Holocene sediments came mainly from the Changjiang River based on compositions of REEs and most trace elements. Some heavy metals are more enriched in the surface sediment than in the deltaic sediments, reflecting human impact. Elemental compositions of the river channel sediment are related to the influence of proximal sediments. Sedimentary environments exert some influences on elemental compositions. Some chemical indices can be used to record chemical weathering undergone by the Changjiang sediment and environmental change.     

Miniature flow injection analyser for laboratory, shipboard and in situ monitoring of nitrate in estuarine and coastal waters

A miniature, submersible flow injection analyser, with solid-state spectrophotometric detection, for the in situ determination of nitrate is described. It utilises the standard laboratory chemistry of cadmium reduction followed by diazotisation. The detection limit was 2.8 μg l⁻¹ N and the linear range could be varied from 2.8 to 100 μg l⁻¹ N up to 100–2000 μg l⁻¹ N to suit local environmental conditions. The versatility of the instrument is demonstrated by results from laboratory, shipboard (North Sea IMPACT Cruise) and in situ (Tamar Estuary, UK) deployments. They show the excellent temporal and spatial resolution that can be achieved for studying dynamic processes in estuarine and coastal waters. The results acquired during the IMPACT Cruise map the transport of nitrate from the Humber Estuary into the North Sea and show that nitrate uptake was more pronounced in areas of shallow and clear waters (Dogger Bank) than in the coastal mixing zone with higher suspended solids. A key feature of the analyser is its portability and ease of deployment due to the small size and weight and low buoyancy. Accuracy was assessed by participation in an international intercomparison exercise and the results were within the assigned tolerance interval of the consensus mean (Z<2).     

The determination of trace metals in estuarine and coastal waters using a voltammetric in situ profiling system

This work presents the optimisation, validation and field deployment of a voltammetric in situ profiling (VIP) system for the simultaneous determinations of dynamic Cd(II), Cu(II) and Pb(II) in estuarine and coastal waters. Systematic studies in NaNO3 (as a supporting electrolyte) and seawater, indicated that variations in ionic strength, pH and dissolved oxygen did not affect the response of the instrument, whereas an Arrhenius type temperature response was observed. The VIP instrument allows the determination of 2-3 samples h(-1), and has a detection limit (defined as 3sigma) in seawater for Cd(II): 23 pM, Cu(II): 1.13 nM, and Pb(II): 23 pM. The VIP system accurately measured the total dissolved concentrations of Cd(II), Cu(II) and Pb(II) in two certified reference materials; SLRS-3, a river water, and SLEW-2, an estuarine water. Field evaluation of the instrumentation and analytical methods was achieved through a series of surveys in the Plym Estuary (Devon, UK), from which environmental data are presented.     

Miniaturized Salinity Gradient Energy Harvesting Devices

Harvesting salinity gradient energy, also known as “osmotic energy” or “blue energy”, generated from the free energy mixing of seawater and fresh river water provides a renewable and sustainable alternative for circumventing the recent upsurge in global energy consumption. The osmotic pressure resulting from mixing water streams with different salinities can be converted into electrical energy driven by a potential difference or ionic gradients. Reversed-electrodialysis (RED) has become more prominent among the conventional membrane-based separation methodologies due to its higher energy efficiency and lesser susceptibility to membrane fouling than pressure-retarded osmosis (PRO). However, the ion-exchange membranes used for RED systems often encounter limitations while adapting to a real-world system due to their limited pore sizes and internal resistance. The worldwide demand for clean energy production has reinvigorated the interest in salinity gradient energy conversion. In addition to the large energy conversion devices, the miniaturized devices used for powering a portable or wearable micro-device have attracted much attention. This review provides insights into developing miniaturized salinity gradient energy harvesting devices and recent advances in the membranes designed for optimized osmotic power extraction. Furthermore, we present various applications utilizing the salinity gradient energy conversion.     

234Th-based measurements of particle flux in surface water of the Bransfield Strait, western Antarctica

Measurements of particulate and dissolved ²³⁴Th were carried out in March 2002 in the Bransfield Strait located between the Antarctic Peninsula and the South Shetland Islands. The ²³⁴Th/²³⁸U disequilibrium found in the upper water column has allowed evaluation of downward particle fluxes across a frontal zone, which divides water masses coming from the Bellingshausen Sea and the Weddell Sea. The highest particle flux has been found in this mixing zone, where it was 3–5 times greater than in the adjacent waters. Total mass fluxes in the upper 150-m water column were estimated as about 2.2 g m^?2 day^?1 in the eastern part of the Strait and 3.1 g m^?2 day^?1 in the western area.     

Influence of water filtration on the determination of a wide range of dissolved contaminants at parts-per-trillion levels

The adsorption of dissolved organic contaminants on glass fibre filters throughout water dissolved/particulate phase decoupling studies was examined. A total of 49 different compounds were considered at low concentration levels (ng L⁻¹), including PAHs, PCBs, organochlorine and organophosphorus pesticides, triazines, thiocarbamates, pyrethroids, phosphate esters and caffeine. Their adsorption on the filters was positively correlated with their log Kow and solubilities, indicating that filter adsorption increased with hydrophobicity. The influence of water properties (i.e. salinity and dissolved organic carbon (DOC) content) was also studied by means of a star experimental design (n = 11). Salinity was the main factor in increasing the adsorption, due to the salting out effect. The influence of DOC suggested that part of the contaminant losses during water filtration may have been caused by the retention on the organic matter adsorbed on the filter surface. Nevertheless, a decrease in filter retention was observed for water with the highest DOC contents, which was probably due to an enhancement of the contaminant solubility in these conditions. Although several factors may control the adsorption process in naturally occurring waters, the extent of the retention of dissolved target analytes on the glass fibre filters should not be underestimated in the analysis of hydrophobic contaminants in marine and estuarine waters at very low concentrations (ppt level).     

Environmental controls of UV-B radiation in forested streams of northern Michigan

We examined UV-B radiation flux and its environmental control within and among streams of northern Michigan. UV-B flux was estimated in streams by plastic dosimetry strips, which allow for the simultaneous and repeated in situ measurement of solar radiation. During the summer of 2004, UV-B flux was measured across depth gradients and along longitudinal transects in seven streams, which were chosen to encompass a range of dissolved organic carbon (DOC) concentrations and canopy cover. Attenuation coefficients of UV-B (K(d) (UV-B)) were estimated using plastic dosimeters placed along a depth gradient. K(d UV-B) were positively correlated with DOC concentration and similar to values obtained with laboratory and in situ spectrometry. Along 100 m longitudinal transects, UV-B flux varied along all streams regardless of their canopy cover and DOC concentration. Within-stream fluxes of UV-B were correlated to canopy cover in the only two streams that both had relatively low DOC concentration and variable canopy cover. Large differences were found among streams in the average UV-B flux (corrected for incident solar flux) reaching the dosimeters at 5 cm depth. These among-stream differences were largely accounted for by the stream width, canopy cover, and DOC concentration. Our results illustrate an inherent variability in UV-B flux within and among streams of northern Michigan that is strongly tied to the interactions of DOC concentration, stream size and riparian vegetation.     

Short-team stability of trace metals in estuarine water samples

The short-term (up to 24 h) stability of estuarine water with high (22%?) and low (<21%?) salinity, stored unacidified in polythene containers prior to filtration, preservation and determination of dissolved trace metals, was assessed. For the-salinity sample a massive (140%) increase in copper concentration was observed, indicating desorption from the particulate phase; a similar, although less pronounced (11%) effect was found for the high-salinity sample, Evidence was also obtained for a significant loss (30%) of lead from a pre-filtered low-salinity sample, suggesting appreciable adsorption to the container walls. For cadmium and nickel, no substantial changes in concentration were observed.     

The Rapid Determination of Orthophosphate,Sulfate, and Chloride in Natural Water Samples With High Iron Concentrations Using Ion Chromatography

Abstract

A rapid procedure has been developed for the analysis of orthophosphate, sulfate and chloride in riverine sediment interstitial water samples which have dissolved iron concentrations ranging from 0.5–2 mmol L^?1. Interferences caused by the precipitation of iron hydroxides resulting from air oxidation of ferrous iron in the anoxic samples and from the alkaline working pH range (9.0 – 10.5) of the Dionex¹ ion chromatographic system were eliminated by complexing the iron with cyanide. Orthophosphate concentration values are compared with dissolved reactive phosphate concentration data for the same samples. Orthophosphate concentrations rather than dissolved reactive phosphate concentrations are preferred for phosphate mineral solubility calculations and for phosphorus nutrient measurements.     

Multielemental speciation of trace elements in estuarine waters with automated on-site UV photolysis and resin chelation coupled to inductively coupled plasma mass spectrometry

An integrated approach for the accurate determination of total, labile and organically bound dissolved trace metal concentration in the field is presented. Two independent automated platforms consisting of an ultraviolet (UV) on-line unit and a chelation/preconcentration/matrix elimination module were specifically developed to process samples on-site to avoid sample storage prior to inductively coupled plasma mass spectrometry (ICP-MS) analysis. The speciation scheme allowed simultaneous discrimination between labile and organic stable dissolved species of seven trace elements including Cd, Cu, Mn, Ni, Pb, U and Zn, using only 5 ml of sample with detection limits ranging between 0.6 ng l⁻¹ for Cd and 33 ng l⁻¹ for Ni. The influence of UV photolysis on organic matter and its associated metal complexes was investigated by fluorescence spectroscopy and validated against natural samples spiked with humic substances standards. The chelation/preconcentration/matrix elimination procedure was validated against an artificial seawater spiked sample and two certified reference materials (SLRS-4 and CASS-4) to ensure homogenous performance across freshwater, estuarine and seawater samples. The speciation scheme was applied to two natural freshwater and seawater samples collected in the Adour Estuary (Southwestern, France) and processed in the field. The results indicated that the organic complexation levels were high and unchanged for Cu in both samples, whereas different signatures were observed for Cd, Mn, Ni, Pb, U and Zn, suggesting organic ligands of different origin and/or their transformation/alteration along estuarine water mixing.