Dynamics of suspended sediment exchange and transport in a degraded mangrove creek in Kenya

This study focuses on sediment exchange dynamics in Mwache Creek, a shallow tidal mangrove wetland in Kenya. The surface area of the creek is 17 km2 at high water spring. The creek experiences semidiurnal tides with tidal ranges of 3.2 m and 1.4 m during spring and neap tides, respectively. The creek is ebb dominant in the frontwater zone main channel and is flood dominant in the backwater zone main channel. During rainy season, the creek receives freshwater and terrigenous sediments from the seasonal Mwache River. Heavy supply of terrigenous sediments during the El Ni?o of 1997-1998 led to the huge deposition of sediments (10(60 tonnes) in the wetland that caused massive destruction of the mangrove forest in the upper region. In this study, sea level, tidal discharges, tidal current velocities, salinity, total suspended sediment concentrations (TSSC) and particulate organic sediment concentrations (POSC) measured in stations established within the main channel and also within the mangrove forests, were used to determine the dynamics of sediment exchange between the frontwater and backwater zones of the main channel including also the exchange with mangrove forests. The results showed that during wet seasons, the high suspended sediment concentration associated with river discharge and tidal resuspension of fine channel-bed sediment accounts for the inflow of highly turbid water into the degraded mangrove forest. Despite the degradation of the mangrove forest, sediment outflow from the mangrove forest was considerably less than the inflow. This caused a net trapping of sediment in the wetland. The net import of the sediment dominated in spring tide during both wet and dry season and during neap tide in the wet season. However, as compared to heavily vegetated mangrove wetlands, the generally degraded Mwache Creek mangrove wetland sediment trapping efficiency is low as the average is about 30% for the highly degraded backwater zone mangrove forest and 65% in the moderately degraded frontwater zone mangrove forest.     

Estimation of the net air-sea flux of ammonia over the southern bight of the North Sea

Measurements of airborne gaseous ammonia and total dissolved ammonium in sea water determined on cruises on the North Sea have been used to calculate net fluxes of ammonia between air and sea. The system is finely balanced with the majority of net fluxes from air to sea, but some periods occur when the sea becomes a net source of ammonia in air. Examination of the field data suggests that the main factor determining the direction of flux is the airborne ammonia concentration, which when elevated causes ammonia deposition to the sea. It is calculated that ammonia deposition to the southern bight of the North Sea (below 56°N) amounts to 7.6 x 103 tonnes N per year, about one-half of an earlier upper limit estimate. Comparison with studies from the Pacific Ocean, in which the sea acts as a source of atmospheric ammonia, reveals that the major differences arise from much higher concentrations of airborne ammonia in the North Sea atmosphere caused by advection from adjacent land.     

Increasing atmospheric antimony contamination in the northern hemisphere: snow and ice evidence from Devon Island, Arctic Canada

Adopting recently developed clean laboratory techniques, antimony (Sb) and scandium (Sc) deposition were measured in a 63.72 m-long ice core (1842-1996) and a 5 m deep snow pit (1994-2004) collected on Devon Island, Canadian High Arctic. Antimony concentrations ranged from 0.07 to 108 pg g(-1) with a median of 0.98 pg g(-1)(N= 510). Scandium, used as a conservative reference element, revealed that dust inputs were effectively constant during the last 160 years. The atmospheric Sb signal preserved in the ice core reflects contamination from industrialisation, the economic boom which followed WWII, as well as the comparatively recent introduction of flue gas filter technologies and emission reduction efforts. Natural contributions to the total Sb inventory are negligible, meaning that anthropogenic emissions have dominated atmospheric Sb deposition throughout the entire period. The seasonal resolution of the snow pit showed that aerosols deposited during the Arctic winter, when air masses are derived mainly from Eurasia, show the greatest Sb concentrations. Deposition during summer, when air masses come mainly from North America, is still enriched in Sb, but less so. Snow and ice provide unambiguous evidence that enrichments of Sb in Arctic air have increased 50% during the past three decades, with two-thirds being deposited during winter. Most Sb is produced in Asia, primarily from Sb sulfides such as stibnite (Sb2S3), but also as a by-product of lead and copper smelting. In addition there is a growing worldwide use of Sb in automobile brake pads, plastics and flame retardants. In contrast to Pb which has gone into decline during the same interval because of the gradual elimination of gasoline lead additives, the enrichments of Sb have been increasing and today clearly exceed those of Pb. Given that the toxicity of Sb is comparable to that of Pb, Sb has now replaced Pb in the rank of potentially toxic trace metals in the Arctic atmosphere.     

Representativity of a Mid-lake Surface Water Chemistry Sample

A mid-lake sample is the conventional sampling strategy used in lake chemistry monitoring programs. Hence, addressing the question of how representative a mid-lake sample is of in-lake conditions is important for interpreting changes in long-term monitoring programs. Our hypotheses were that; (i) the location of a sampling site within a lake will affect its representativity and (ii) a mid-lake sample could be considered representative of average surface water physico-chemistry. We focused on the surface water chemistry in 34 Swedish lakes. To obtain a wide diversity of lake types, the lakes were classified according to mean depth, water residence time, and three main ecoregions. Two sampling seasons were selected, representative of high and low biological activity and stratified and non-stratified conditions, respectively. Ten samples were collected in each lake. The mid-lake samples differed significantly from the nine remaining samples in less than 4% of the total number of two-sample t-tests performed. Samples collected close to lake inlets differed from the other samples more often than samples collected in the central parts of the lakes. We concluded that the location of a sampling site within a lake may affect the sample's representativity of lake water chemistry, and that a mid-lake surface water sample could be considered representative of surface water chemistry.     

Carbon Tetrachloride Marine Risk Assessment with Special Reference to the Osparcom Region: North Sea

Accurate estimates of stressor levels in unsampled streams would provide valuable information for managing these resources over large regions. Spatial interpolation of stream characteristics have rarely been attempted, partly because defining separation distances between distinct stream samples is not straightforward. That is, conventional Eulerian definitions of separation distance may not apply to stream networks where information flows along distinct paths. A two-stage model for estimating stressor levels in unsampled streams is presented. Mean characteristics within streams are predicted usign a generalized additive model and residual variation is estimated using a conventional application of spatial statistics. The model is developed and tested using stream survey data collected in the state of Maryland, USA. Model efficiency is compared for three stream variables (nitrate concentration, sulfate concentration, and epifaunal substrate score) known to be associated with biological impairments in streams. Accounting for spatial autocorrelation in the residual variation improved model R2 from 0.71 to 0.81 for nitrate, from 0.29 to 0.63 for sulfate, and from 0.21 to 0.31 for epifaunal substrate score.     

1,4-Dichlorobenzene Marine Risk Assessment with Special Reference to the Osparcom Region: North Sea

This risk assessment on 1,4-dichlorobenzene was carried out for the marine environment, following methodology given in the EU risk assessment Regulation (1488/94) and Guidance Document of the EU New and Existing Substances Regulation (TGD, 1996). Data from analytical monitoring programs in large rivers and estuaries in the North Sea area were collected and evaluated on effects and environmental concentrations. Risk is indicated by the ratio of predicted environmental concentration (PEC) to predicted no-effect concentration (PNEC) for the marine aquatic environment. In total, 17 data for fish, 9 data for invertebrates and 7 data for algae were evaluated. Acute and chronic toxicity studies were taken into account and appropriate assessment factors used to define a final PNEC value of 20 microg/l. Recent monitoring data indicate that 1,4-dichlorobenzene levels in coastal waters and estuaries are below the determination limit of 0.1 microg/l used in monitoring programs. The worst case value recorded in river water is below 0.45 microg/l. Using these values, calculated PEC/PNEC ratios give safety margins of about 40-200, taking no account of dilution in the sea. Environmental fate and bioaccumulation data indicate that current use of 1,4-dichlorobenzene poses no risk to the aquatic environment.     

Assessing the removal of inorganic colloids and Cryptosporidium parvum from drinking water

A new batch device that simulates the conditions in water and wastewater treatment plants and enables the study of low-concentration feeds is described. The application of this apparatus to the monitoring of the concentration of inorganic and/or biological contaminants is demonstrated, using kaolin particles and Cryptosporidium parvum oocysts, respectively. The rate of inorganic particle attachment to the static medium is found to be directly proportional to the initial influent concentration. On the other hand, Cryptosporidium parvum removal is found to be more effective in the presence of additional (kaolin) particles, and this is attributed to electrostatic interactions between oppositely charged layers on the absorbing medium. Accordingly, the addition of humic materials is found to inhibit the removal process, possibly by neutralizing the positive charge on the kaolin particles. The relevance of these results to existing water purification processes in general and to risk assessment of microbiological contamination in particular is discussed.     

La chimie du plomb et du brome particulaire en atmosphere urbaine: II — Effets locaux

In an abnormal urban atmospheric situation, where we have detected an exceptional increasing of lead concentration which could have no relation to traffic modification, we have been able to detect others sources, that has been possible thanks to simultaneous studies of granulometric distribution and concentrations of lead and bromine in this particular atmosphere.     

Potential for reducing indoor styrene exposure from copied paper through use of low-emitting toners

Tests were conducted using 53-L dynamic chambers to determine airborne styrene emission rates over time from freshly copied paper. Copies were produced on a single photocopier using two toners manufactured for this copier but having different styrene contents. The resulting emission models were used to predict whether indoor styrene concentrations resulting from copied paper in a typical office might be significantly reduced by use of a low-emitting toner for a given copier. The styrene emissions were best represented by either a 3rd-order decay model or by a power law model having an exponent between 0.3 and 0.5 (R2 = 0.94-0.99). The two toners resulted in copied paper having significantly different styrene emissions (p < 0.01), with unit mass emissions over 1000 hr being nine times greater with the higher-emitting toner. But copied paper is predicted to produce peak indoor styrene concentrations in a typical office no more than 1% of the World Health Organization health-based guideline. Thus, for the toners considered here, indoor styrene exposures from copied paper appear to be too limited to provide incentive for switching to the lower-emitting toner. The ability to generalize these conclusions is limited by the fact that only one copier and two toners could be tested.     

Distribution of antimony in contaminated grassland: 2--Small mammals and invertebrates

Concentrations of antimony in invertebrates and small mammals from grasslands in the vicinity of an antimony smelter were significantly elevated compared to a control site. Higher concentrations of antimony were recorded in liver, lung and kidney tissue of herbivorous and insectivorous mammals from the contaminated sites. However, there is little evidence of bioaccumulation of antimony in food chains represented by the soil-vegetation-invertebrate-insectivore pathway of the grasslands, and little indication of significant accumulation by herbivorous mammals despite marked contamination of their diet.