High mortality of the larvae of the common mussel at low concentrations of tributyltin

Laboratory reared veliger larvae of the common mussel Mytilus edulis were grown for 15 days in filtered seawater containing 10 μg l^?1, 1 μg l^?1 and 0.1 μg l^?1 tributyltin oxide (TBTO), the biocide in recent antifouling paint formulations. No larvae survived longer than 5 days in 10 μg l^?1 TBTO or 10 days in 1 μg l^?1 TBTO. Approximately half the larvae subjected to 0.1 μg l^?1 TBTO were dead by day 15 (approximate 15 day LC₅₀ = 0.1 μg l^?1 TBTO) and most of the surviving larvae were moribund and had grown significantly more slowly than controls. It is noted that current recorded levels of TBT at several UK estuarine sites are higher than 0.1 μg l^?1 and there has therefore probably been a high mortality of mussel larvae at such sites. The results are discussed in relation to the reported short-term toxicity of organotins to other marine organisms and the value of carrying out longer-term tests at low levels of TBT is pointed out.     

Acute toxicity of bis(tributyltin) oxide to a marine copepod

A static renewal toxicity test was conducted to evaluate the response of the copepod Acartia tonsa to bis(tributyltin) oxide (TBTO), the active compound of recently developed antifouling paints. Copepods were individually placed in test tubes containing 4 ml of 0.3, 0.5, 1.0, 1.7 or 3.0 μg l^?1 TBTO with acetone and seawater. Thirty copepods were used for each treatment and control condition and all solutions were renewed daily. The 96-h LC₅₀ was 1.0 μg l^?1 with a 95% confidence interval between 0.8 and 1.2 μg l^?1 TBTO. The 144-h EC₅₀ was 0.4 μg l^?1 TBTO which approaches concentrations recently measured in San Diego Bay. Some copepods exposed to 0.3 μg l^?1 TBTO became moribund after six days.     

Shell thickening in Crassostrea gigas: Organotin antifouling or sediment induced?

Crassostrea gigas spat were cultured for 8 weeks in the presence of a mixed algal diet in experimental tanks containing bis (tributyl tin) oxide (TBTO) alone, TBTO and a marine sediment, or a marine sediment alone. Growth measurements taken on a weekly basis showed enhanced weight gain in oysters exposed to nominal 50 and 100 mg l^?1 concentrations of marine sediment alone. Spat in low level TBTO treatments (0.15 μg l^?1) grew less well than the controls and showed pronounced thickening of the upper shell valve. High levels of TBTO (1.6 μg l^?1) severely inhibited oyster growth. Tissue concentrations of TBT compounds were measured at the end of the experiment. Bio-concentration factors of 3000- and 10000-fold were demonstrated for the high and low TBTO treatments respectively.     

The effect of tributyltin oxide on growth of Mytilus edulis

Juvenile Mytilus edulis were exposed to 0.1–10.0 μg TBTO l⁻¹ in flowing raw seawater, and the shell length growth was measured in 24–48 h intervals for 7 days. Significant reductions in length growth rate occurred at ≥0.4 μg TBTO l⁻¹. The relationship between TBTO concentration and growth response is approximately hyperbolic.     

Occurrence and distribution of hydrocarbons in the surface microlayer and subsurface water from the urban coastal marine area off Marseilles, Northwestern Mediterranean Sea

Aliphatic (AHs) and polycyclic aromatic hydrocarbons (PAHs) were analyzed in dissolved and particulate material from surface microlayer (SML) and subsurface water (SSW) sampled at nearshore observation stations, sewage effluents and harbour sites from Marseilles coastal area (Northwestern Mediterranean) in 2009 and 2010. Dissolved and particulate AH concentrations ranged 0.05–0.41 and 0.04–4.3 μg l⁻¹ in the SSW, peaking up to 38 and 1366 μg l⁻¹ in the SML, respectively. Dissolved and particulate PAHs ranged 1.9–98 and 1.9–21 ng l⁻¹ in the SSW, amounting up 217 and 1597 ng l⁻¹ in the SML, respectively. In harbours, hydrocarbons were concentrated in the SML, with enrichment factors reaching 1138 for particulate AHs. Besides episodic dominance of biogenic and pyrogenic inputs, a moderate anthropisation from petrogenic sources dominated suggesting the impact of shipping traffic and surface runoffs on this urbanised area. Rainfalls increased hydrocarbon concentrations by a factor 1.9–11.5 in the dissolved phase.     

Sublethal effects of bis(tri-n-butyltin)oxide on Crassostrea gigas spat

Hatchery produced spat of the Pacific Oyster Crassostrea gigas were exposed to low levels of bis(tri-n-butyltin)oxide (TBTO) 0.2, 0.1, 0.05, 0.02, and 0.01 μg I⁻¹. Their oxygen consumption, feeding rate, compensation for hypoxia, and growth rate was examined after exposure to TBTO and compared to their performance prior to this. In all cases highly significant relationships between TBTO concentration and the physiological variable in question were observed. Significant effects were found down to levels of 0.05 μg I⁻¹ for oxygen consumption and feeding rate, to 0.02 μg I⁻¹ for growth and to 0.01 μg I⁻¹ for compensation for hypoxia. These levels are far lower than those reported for many UK sites and the results are discussed in relation to the possible environmental impact of the observed effects.     

Trace metal levels in coastal sea water investigation of Danish waters

The concentration levels of Cd (25 ng l^?1), Cu (0.45 μg l^?1), Ni (0.48 μg l^?1), Fe (0.2–7.0 μg l^?1), Pb (40 ng l^?1) and Zn (0.80 μg l^?1) have been determined in the Danish Sounds and in the Kattegat. Different sampling techniques have been used and analyses have been carried out separately by two different investigators, both using freon-extraction followed by determination by atomic absorption spectrometry (a.a.s.). Except for iron, found mainly in the particulate phase, the metals are found predominantly in a dissolved and labile (extractable) form. The results are compared with trace metal levels found in the two main water masses entering the Kattegat—the North Sea and the Baltic Sea.     

Oil pollution on the Egyptian Red Sea coast

A simple weighing method using carbon tetrachloride as solvent was used to survey the dissolved hydrocarbon and tarball levels in the area of the Egyptian Red Sea coast. The area of investigation covers the coastal area from Ras-Gharib down to the port of Qosier during the period from September 1979 to February 1981. This survey confirms the presence of extensive oil pollution in the area, especially at Ras-Gharib and Ras-Shukhair. Minimum concentrations were obtained at Ghardaqa where no dissolved hydrocarbons were detected (i.e. less than 10 μg l^?1) in 1979–1980 but an increase to 20 μg l^?1 in 1981 was recorded. The high levels of pollution recorded in the southern part of the Gulf of Suez are related to the presence of the offshore oil fields, most of which are located at Ras-Gharib.     

Trace metal distributions in Saint John Harbour sediments

The concentration and areal distribution of selected trace metals (Cu, Zn, Pb, Cd, Mo, Ni, Mn and Hg) in surficial sediments of Saint John Harbour, New Brunswick, Canada, were studied to determine the extent of anthropogenic input and to estimate the effects of dumping dredged material in the outer harbour. Hg and Cd are of especial concern, since the disposal of dredge material containing these two elements is regulated under the Ocean Dumping Control Act.The concentrations of all metals are low: Cu 16, Zn 53, Pb 24, Cd 0.16, Mo 3, Ni 16, Mn 296 and Hg 0.04 μg g^?1. Hg and Cd levels in sediments are well below the permissible limits of 0.75 and 0.6 μg g^?1, respectively, set by the Ocean Dumping Control Act.The mean concentrations of trace elements are similar to the low mean values in the unpolluted Bay of Fundy. There is an overall decline in concentrations of metals in the sediments from the inner to the outer harbour. Comparison of the metal levels in the sediments from different areas within the harbour indicate that there is a detectable anthropogenic input in the Courtenay Bay area. Trace metal levels at the dumpsite are significantly lower than in the Courtenay Bay area, where the bulk of the dredged material originates.     

Enhanced mercury tolerance in marine mussels and relationship to low molecular weight,mercury-binding proteins

Pre-exposure of marine mussels to low levels of mercury (0.5 μg l^?1 and less) enhanced their tolerance to more toxic levels. Seawater mercury concentrations similar to our experimental pre-exposure levels have been reported in mercury-contaminated areas where mussels presently exist. A higher pre-exposure concentration (5 μg l^?1) was not effective in inducing enhanced mercury tolerance. The relative effectiveness of pre-exposure concentration in inducing enhanced tolerance was related to induction of mercury-binding proteins, the degree of saturation of mercury on the proteins, and the extent of binding of mercury to other subcellular fractions.     

The occurrence of arsenic in selected marine macroalgae from two coastal areas of South Australia

Total arsenic concentrations have been measured in macroalgae specimens from two coastal areas of South Australia. Phaeophyta in both areas were found to contain elevated arsenic concentrations (42.2–179 μg g^?1 and 26.3–65.3 μg g^?1) relative to Rhodophyta (17.6–31.3 μg g^?1 and 12.5–16.2 μg g^?1) and Chlorophyta (6.3–16.3 μg g^?1 and 9.9–10.8 μg g^?1).     

Hydrocarbon concentrations in water and sediments from UK marine waters,determined by fluorescence spectroscopy

Between January 1978 and September 1979 samples of subsurface (1 m) water and surface sediment were collected from sites in the North Sea, English Channel, Irish Sea and a number of estuarine areas. These have been analysed by fluorescence spectroscopy (UVF) in order to provide information on the levels of hydrocarbons generally present in UK marine waters.Total hydrocarbon concentrations (THCs) of water samples ranged from 1.1–74 μg l.^?1 Ekofisk crude oil equivalents, all values greater than 3.5 μg l.^?1 occurring inshore. In offshore areas the mean THCs were: 1.3 μg l.^?1 in the northern North Sea, 1.5 μg l.^?1 in the western Channel, 2.5 μg l.^?1 in the eastern Channel and southern North Sea, and 2.6 μg l.^?1 in the Irish Sea.THCs of sediment samples ranged from 0.27–340 μ g^?1 dry weight Ekofisk crude oil equivalents, the highest concentration being in the Queen's Channel, the main entrance to the River Mersey.     

Amenability of nitrilotriacetic acid to biodegradation in a marine simulation

The behaviour of the detergent builder nitrilotriacetic acid (NTA) has been studied in the presence of a marine bacterial population potentially associated with a sewage discharge to coastal waters. Additions of 500 μg l^?1 NTA were made over a period of 80 days and 7500 μg l^?1 NTA over 40 days in both aerobic and anoxic environments. It was concluded that NTA was not degraded at either concentration under aerobic or anoxic conditions, despite the presence of a significant bacterial population under aerobic conditions. Possible effects of NTA recalcitrance and its accumulation in coastal marine waters are discussed.     

Petroleum hydrocarbons in the arctic ocean surface water

The concentration of petroleum hydrocarbons in Arctic surface water under the ice north of Svalbard has been determined by fluorescence spectrofluorometry using three different excitation/emission wavelength combinations. With Kuwait crude oil as a reference, the concentration range is 0.1–0.6 μg l^?1 crude oil equivalents with respect to light molecular weight components and 0.05–0.2 μg l^?1 heavy molecular weight components.     

CONTROLS ON SURFACE WATER CHEMISTRY IN THE UPPER MERCED RIVER BASIN,YOSEMITE NATIONAL PARK,CALIFORNIA

Surface water draining granitic bedrock in Yosemite National Park exhibits considerable variability in chemical composition, despite the relative homogeneity of bedrock chemistry. Other geological factors, including the jointing and distribution of glacial till, appear to exert strong controls on water composition. Chemical data from three surface water surveys in the upper Merced River basin conducted in August 1981, June 1988 and August 1991 were analysed and compared with mapped geological, hydrological and topographic features to identify the solute sources and processes that control water chemistry within the basin during baseflow. Water at most of the sampling sites was dilute, with alkalinities ranging from 26 to 77 μequiv. l⁻¹. Alkalinity was much higher in two subcatchments, however, ranging from 51 to 302 μequiv. l⁻¹. Base cations and silica were also significantly higher in these two catchments than in the rest of the watershed. Concentrations of weathering products in surface water were correlated to the fraction of each subcatchment underlain by surficial material, which is mostly glacial till. Silicate mineral weathering is the dominant control on concentrations of alkalinity, silica and base cations, and ratios of these constituents in surface water reflect the composition of local bedrock. Chloride concentrations in surface water samples varied widely, ranging from <1 to 96 μequiv. l⁻¹. The annual volume-weighted mean chloride concentration in the Merced River at the Happy Isles gauge from 1968 to 1990 was 26 μequiv. l⁻¹, which was five times higher than in atmospheric deposition (4–5 μequiv. l⁻¹), suggesting that a source of chloride exists within the watershed. Saline groundwater springs, whose locations are probably controlled by vertical jointing in the bedrock, are the most likely source of the chloride. Sulphate concentrations varied much less than most other solutes, ranging from 3 to 14 μequiv. l⁻¹. Concentrations of sulphate in quarterly samples collected at the watershed outlet also showed relatively little variation, suggesting that sulphate may be regulated to some extent by a within-watershed process, such as sulphate adsorption.     

Flood‐based analysis of high‐magnitude sediment transport using a non‐parametric method

Upland erosion and the resulting reservoir siltation is a serious issue in the Isábena catchment (445 km² Central Spanish Pyrenees). During a three‐month period, water and sediment fluxes have been monitored at the catchment outlet (Capella), two adjacent subcatchments (Villacarli, 41 km²; Cabecera, 145 km²) and the elementary badland catchment Torrelaribera (8 ha). This paper presents the results of the monitoring, a method for the calculation of a sedigraph from intermittent measurements and the derived sediment yields at the monitored locations. The observed suspended sediment concentrations (SSCs) demonstrate the role of badlands as sediment sources: SSCs of up to 280 g l^?1 were encountered for Villacarli, which includes large badland areas. SSCs at the Cabecera catchment, with great areas of woodland, barely exceeded 30 g l^?1. SSCs directly at the sediment source (Torrelaribera) were comparable to those at Villacarli, suggesting a close connection within this subcatchment. At Capella, SSCs of up to 99 g l^?1 were observed. For all sites, SSC displayed only a loose correlation with discharge, inhibiting the application of a simple sediment rating curve. Instead, ancillary variables acting as driving forces or proxies for the processes (rainfall energy, cumulative discharge, rising/falling limb data) were included in a quantile regression forest model to explain the variability in SSC. The variables with most predictive power vary between the sites, suggesting the predominance of different processes. The subsequent flood‐based calculation of sediment yields attests high specific sediment yields for Torrelaribera and Villacarli (6277 and 1971 t km^?2) and medium to high yields for Cabecera and Capella (139 and 410 t km^?2) during the observation period. In all catchments, most of the sediment was exported during intense storms of late summer. Later flood events yield successively less sediment. Relating upland sediment production to yield at the outlet suggests considerable effects of sediment storage within the river channel. Copyright © 2008 John Wiley & Sons, Ltd.     

Dissolved petroleum hydrocarbon in the northwestern Arabian Gulf

Mean concentrations of total hydrocarbons were 2.95, 4.14 and 3.29 μg l⁻¹ in seawater of Kuwait, Saudi Arabia and Qatar respectively. High concentrations were measured at the northern coasts of Qatar. Northern coasts of Qatar were found to be affected directly by water advected from Saudi Arabia seawater through the water circulation in this area. High concentration of oil (546.4 μg l⁻¹) was detected at the area in front of pipelines extended from Ras Tanura and Ju'aymah centres of oil production and exportation in the Arabian Gulf. This high concentration was detected in the north coast of Qatar after a period of 44 days indicating current speed of 5 cm s⁻¹ prevailing in this area.     

Concentrations of unsubstituted polycyclic aromatic hydrocarbons in softshell clams from Coos Bay,Oregon, USA

Concentrations of benzo[a]pyrene (BAP) were measured in subpopulations of softshell clams, Mya arenaria, from four intertidal sites in Coos Bay from June 1976 to June 1978. Subsequently, concentrations of 15 unsubstituted polynuclear aromatic hydrocarbons (PNAH) were determined in two subpopulations from September 1978 to August 1979. There were significant differences between BAP concentrations in clams from the four sites. For the two-year period, they were highest in clams inhabiting areas adjacent to the industrialized bayfront and lowest in clams inhabiting more remote areas. There were no significant seasonal variations in BAP concentrations during this period. During the 1978–1979 study, the average total PNAH concentration in clams from the bayfront area was 555.1 μg kg^?1 compared to 76.3 μg kg^?1 for clams from a more remote environment. In general, PNAH concentrations were lowest in the fall-winter and highest during the spring-summer.     

The solute budget of a forest catchment and solute fluxes within a Pinus radiata and a secondary native forest site,southern Chile

Solute concentrations and fluxes in rainfall, throughfall and stemflow in two forest types, and stream flow in a 90 ha catchment in southern Chile (39°44′S, 73°10′W) were measured. Bulk precipitation pH was 6·1 and conductivity was low. Cation concentrations in rainfall were low (0·58 mg Ca²⁺ l^?1, 0·13 mg K⁺ l^?1, 0·11 mg Mg²⁺ l^?1 and <0·08 mg NH₄–N l^?1), except for sodium (1·10 mg l^?1). Unexpected high levels of nitrate deposition in rainfall (mean concentration 0·38 mg NO₃–N l^?1, total flux 6·3 kg NO₃–N ha^?1) were measured. Concentrations of soluble phosphorous in bulk precipitation and stream flow were below detection limits (<0·09 mg l^?1) for all events. Stream‐flow pH was 6·3 and conductivity was 28·3 μs. Stream‐water chemistry was also dominated by sodium (2·70 mg l^?1) followed by Ca, Mg and K (1·31, 0·70 and 0·36 mg l^?1). The solute budget indicated a net loss of 3·8 kg Na⁺ ha^?1 year^?1, 5·4 kg Mg²⁺ ha^?1 year^?1, 1·5 kg Ca²⁺ ha^?1 year^?1 and 0·9 kg K⁺ ha^?1 year^?1, while 4·9 kg NO₃–N ha^?1 year^?1 was retained by the ecosystem. Stream water is not suitable for domestic use owing to high manganese and, especially, iron concentrations. Throughfall and stemflow chemistry at a pine stand (Pinus radiata D. Don) and a native forest site (Siempreverde type), both located within the catchment, were compared. Nitrate fluxes within both forest sites were similar (1·3 kg NO₃–N ha^?1 year^?1 as throughfall). Cation fluxes in net rainfall (throughfall plus stemflow) at the pine stand generally were higher (34·8 kg Na⁺ ha^?1 year^?1, 21·5 kg K⁺ ha^?1 year^?1, 5·1 kg Mg²⁺ ha^?1 year^?1) compared with the secondary native forest site (24·7 kg Na⁺ ha^?1 year^?1, 18·9 kg K⁺ ha^?1 year^?1 and 4·4 kg Mg²⁺ ha^?1 year^?1). However, calcium deposition beneath the native forest stand was higher (15·9 kg Ca²⁺ ha^?1 year^?1) compared with the pine stand (12·6 kg Ca²⁺ ha^?1 year^?1). Copyright © 2002 John Wiley & Sons, Ltd.     

High chloride concentrations in the soil and groundwater under an oak hedge in the West of France: an indicator of evapotranspiration and water movement

Chloride is a major anion in soil water and its concentration rises essentially as a function of evapotranspiration. Compared to herbaceous vegetation, high transpiration rates are measured for isolated trees, shelterbelts or hedgerows. This article deals with the influence of a tree hedge on the soil and groundwater Cl^? concentrations and the possibility of using Cl^? as an indicator of transpiration and water movements near the tree rows. Cl^? concentrations were measured over 1 year at different depths in the unsaturated zone and in the groundwater along a transect intersecting a bottomland oak hedge. We observed a strong spatial heterogeneity of Cl^? concentrations, with very high values up to 2 g l^?1 in the unsaturated zone and 1·2 g l^?1 in the upper part of the groundwater. This contrasts with the low and homogeneous concentrations (60–70 mg l^?1) in the deeper part of the groundwater. Cl^? accumulation in the unsaturated zone at the end of the vegetation season allows us to identify the active root zone extension of trees. In winter, upslope of the tree row, downwards leaching partly renews the soil solution in the root zone, while the slow water movement under the trees or farther downslope results in Cl^? accumulation and leads to a salinization of the soil and groundwater. This salinization is of the same order as experimental conditions produce negative effects on oak seedlings. The measurement of Cl^? concentrations in the unsaturated zone under tree rows at the end of the vegetation season would indicate whether certain topographic, pedological or climatic conditions are likely to favour a strong salinization of the soil, as observed in the present study. Copyright © 2009 John Wiley & Sons, Ltd.