Distribution and temporal variation of cadmium in the St. Lawrence river basin

Samples of raw water were collected at regular intevals at two transects in the St. Lawremce River and four of its tributaries from March to November 1991 and from April to June 1992. Water samples were analyzed for both the dissolved and the particulate phase for cadmium (Cd), organic carbon, iron and manganese. Mean dissolved Cd concentration was 10±5 ng/L and no spatial variability was observed. Higher concentrations were found during high flow periods, suggesting an uptake of cadmium by phytoplankton during summer. In addition, dissolved cadmium did not appear to be associated with either DOC, dissolved Fe or dissolved Mn. The mean particulate Cd concentration was 1.3±1.1 μg/g, with almost all stations presenting the same concentration except the Yamaska River, which had a concentration of 0.5±0.2 μg/g. Particulate Cd showed a negative correlation with suspended particulate matter and a positive correlation with particulate organic carbon and particulare manganese. Fifty-nine percent of the cadmium was found to be in the particulate phase. Partition coefficients for cadmium (Kd), organic carbon (Kc), iron (KdFe) and manganese (KdMn) were calculated for each sample. Log Kd varied from 3.9 to 5.9, with an average of 5.0±0.4. Log Kd decreased with increasing particulate, matter as did Log Kc and Log KdMn. No significant correlation was found between Log Kd and Log Kc, suggesting that the distribution of cadmium between the dissolved and the particulate phase is not influenced by the distribution of organic carbon. In contrast, positive correlations were observed between Log Kd, Log KdFe and Log KdMn. Cadmium distribution appears to be influenced by Fe and Mn distribution.     

Iron in the southeastern Bering Sea: Elevated leachable particulate Fe in shelf bottom waters as an important source for surface waters

Surface transects and vertical profiles of total and leachable particulate Fe, Mn, Al and P, along with dissolved and soluble Fe were obtained during August 2003 in the southeastern Bering Sea. High concentrations of leachable particulate Fe were observed in the bottom waters over the Bering Sea shelf with an unusually high percentage of the suspended particulate Fe being leachable. Leachable particulate Fe averaged 81% of total particulate Fe, and existed at elevated concentrations that averaged 23 times greater than dissolved Fe in the isolated cool pool waters over the mid shelf where substantial influence of sedimentary denitrification was apparent. The elevated leachable particulate Fe is suggested to be a result of sedimentary Fe reduction in surficial sediments, diffusion of Fe(II) from the sediments to the bottom waters, and subsequent oxidation and precipitation of reduced Fe in the overlying bottom waters. Eddies and meanders of the Bering Slope Current can mix this Fe-rich water into the Green Belt at the outer shelf-break front. Elevated levels of leachable particulate Fe were observed in surface waters near the Pribilof Islands where enhanced vertical mixing exists. Storm events and/or cooling during fall/winter with the resultant destruction of the thermally stratified two-layer system can also mix the subsurface water into surface waters where the elevated leachable particulate Fe is a substantial source of biologically available Fe.     

The flux of particulate material through a well-mixed estuary

The flux of suspended particulate material across the mouth of a well-mixed estuary was measured over 12 months. Samples were taken over one neap and one spring tidal cycle each month and analysed for total suspended particulate material, inorganic and organic particulates, particulate organic carbon and particulate organic nitrogen. Water volume transport at discrete time-steps were determined by means of a one-dimensional hydrodynamic model, calibrated for each tidal cycle sampled. Net transport varied between tidal cycles with regard to direction (import or export) and magnitude. Annual budgets revealed a net export of 5306 tonne of total suspended particulate material (3900 tonne of inorganic particulates, 1286 tonne of particulate organic carbon and 120 tonne of particulate organic nitrogen). The sources of particulate organic carbon are mainly from saltmarshes (194 g POC m²y¹) and from intertidal invertebrate production (586 g POC m⁻²y⁻¹).     

The Odra River Load of Heavy Metals at Hohenwutzen during the Flood in 1997

The Odra river flood of 1997 was a rare hydrological as well as an interesting sedimentological event. At Hohenwutzen (Lower Odra River) we observed the suspended particulate matter transport and the temporal development of water and solidsπ pollution with heavy metals and As. While the suspended particulate matter concentration decreased the trace element concentrations increased during the flood by fractionation of particles and solution processes. Because of a successive flooding of differently contaminated sedimentary sources and polluted regions the contents of heavy metals developed irregularly. Their median particulate concentrations did not exceed the values of older samples taken under mean discharge conditions between 1989 and 1995. The dissolved amounts correspond to those of the Elbe river in 1990. During the flood the dissolved share of all analyzed total element contents increased. The total loads increased 4fold (Cr) to 17fold (Cd).     

Variability of particulate (SS,POC) and dissolved (DOC,NO3) matter during storm events in the Alegria agricultural watershed

The temporal variability of suspended sediment, nitrates (NO₃) and dissolved (DOC) and particulate organic carbon concentrations was analysed in the Alegria agricultural watershed over a 2‐year period. Nine storm events were studied, including an exhaustive analysis of hydrometeorological conditions, quantification of fluxes, and concentration‐discharge hysteresis loop characterization. The overall aim was to study the variability in these components during storm events and determine the mechanisms (flow paths) affecting the trajectories, from the source to the stream. The forms, rotational patterns and trends of hysteretic loops were investigated, and relationships between hysteresis features and hydrological parameters were studied. The results revealed clear differences between particulate (suspended sediment, particulate organic carbon) and dissolved (DOC, NO₃) matter transport responses. Movement of the particulate matter was attributed to surface water, as reflected in clockwise hysteresis loops, whereas dissolved matter showed, in general, counterclockwise hysteresis loops, indicating a time delay in the arrival of solutes to the stream. This could be related to subsurface flow paths for DOC and a groundwater source for NO₃. Copyright © 2013 John Wiley & Sons, Ltd.     

Mercury distribution in Douro estuary (Portugal)

Determinations of dissolved reactive and total dissolved mercury, particulate and sedimentary mercury, dissolved organic carbon (DOC), particulate organic carbon (POC) and suspended particulate matter (SPM) have been made in the estuary of river Douro, in northern Portugal. The estuary was stratified by salinity along most of its length, it had low concentrations of SPM, typically <20 mg dm(-3), and concentrations of DOC in the range <1.0-1.8 mg dm(-3). The surface waters had a maximum dissolved concentration of reactive mercury of about 10 ng dm(-3), whereas for the more saline bottom waters it was about 65 ng dm(-3). The surface waters had maximum concentrations of total suspended particulate mercury of approximately 7 microg g(-1) and the bottom waters were always <1 microg g(-1). Concentrations of mercury in sediments was low and in the range from 0.06 to 0.18 microg g(-1). The transport of mercury in surface waters was mainly associated with organic-rich particulate matter, while in bottom waters the dissolved phase transport of mercury is more important. Lower particulate organic matter, formation of chlorocomplexes in more saline waters and eventually the presence of colloids appear to explain the difference of mercury partitioning in Douro estuarine waters.     

Long‐term monitoring of a mercury contaminated estuary (Ria de Aveiro,Portugal): the effect of weather events and management in mercury transport

The main aim of this research was to assess the mercury transport from an estuarine basin with a background of anthropogenic contamination during a spring tidal cycle (year 2009) and compare it with two previous tidal cycles (years 1994 and 1999), as part of a long‐term monitoring program. Results showed that effective mercury transport occurs both in the dissolved and particulate fractions (0.18 and 0.20 kg per tidal cycle, respectively), and despite an overall decrease in environmental contamination, results more than double previous findings on particulate transport in the system. These findings result essentially from changes in the tidal prism (net export of 2 million m³ of water), given that both dissolved and particulate concentrations did not increase over time. Hydrodynamic simulations were performed to evaluate the effect of physical disturbance (dredging) and weather events (increased freshwater flow) in these processes, and results suggest the increased freshwater flow into the system as the main forcing function for the mercury transport increment. These results highlight the importance of long‐term monitoring programs, since despite an overall improvement in local contamination levels, the enhancement of transport processes through hydrological changes increases environmental pressure away from the contamination source. Copyright © 2012 John Wiley & Sons, Ltd.     

Speciation of organic carbon,Cu and Mn in the River Marne (France): the role of colloids

The distribution of organic carbon (OC) and of some metals (Cu, Mn) amongst the particulate (>0·2 μm), colloidal (10 kDa–0·2 μm) and the truly dissolved (<10 kDa) fractions of the River Marne was investigated during the phytoplankton spring bloom. A tangential ultrafiltration (UF) device was utilized to separate the colloidal fraction. On average, 22% of the OC, 31% of the Cu and 53% of the Mn, usually assigned to the so‐called dissolved fraction, were found in the colloidal fraction. The colloidal fraction exhibited a behaviour different from that of the particulate and truly dissolved fractions. Autochthonous production led to enrichment in the colloidal and particulate OC pools: up to 47% of the total dissolved OC was in the colloidal fraction. An increase in the colloidal metal fraction, concomitant with a fall in the truly dissolved fraction, coincided with peaks in phytoplankton during the bloom. These phenomena might be related either to an increase in pH associated with photosynthetic activity, resulting in the precipitation of truly dissolved forms into the colloidal fraction, or to scavenging of the truly dissolved metals by the algal species of colloidal size. The interaction between the colloidal and the truly dissolved phases was very important. The partition coefficients of the Cu and Mn between the colloidal and truly dissolved fractions were higher than between the particulate and the truly dissolved fractions. This pattern is consistent with a greater specific surface area of colloids than macroparticles. Consequently, the adsorption and complexation capacities are enhanced in the colloidal fraction of the particulate matter. The extraction of hydrophobic complexes with Cu using C₁₈ Sep‐Pak columns, showed that the Cu occurring in colloidal, total dissolved or truly dissolved forms was significantly complexed by the organic matter. The truly dissolved fraction might be complexed up to 100% during a phytoplankton bloom. Copyright © 1999 John Wiley & Sons, Ltd.     

Spatial and temporal dynamics of stream water particulate and dissolved N, P and C forms along a catchment transect, NE Scotland

The dynamics of dissolved and particulate N, P and organic C were examined for field drains, through a headwater (4 km²), into a mesoscale stream (51 km²) and river (1844 km²) catchment. Distributions of N and P forms were similar in the agricultural headwater and field drains; annual P fluxes of particulate and dissolved forms were of equal magnitude, whilst N was dominated by NO₃–N. Across all scales organic P was an important, often dominant, component of the dissolved P. Temporal variation in nutrient concentrations and proportions was greatest in the headwater, where storms resulted in the generation of large concentrations of suspended particulate matter, particulate and dissolved P, particularly following dry periods. The data suggest that groundwater and minor point source inputs to the mesoscale catchment buffered the temporal variability in hydrochemistry relative to the headwater. Summer low flows were associated with large PO₄–P concentrations in the mesoscale catchment at a critical time of biological sensitivity. At the largest river catchment scale, organic forms of C, N and P dominated. Inorganic nutrient concentrations were kept small through dilution by runoff from upland areas and biological processes converted dissolved N and P to particulate forms. The different processes operating between the drain/headwater to the large river scale have implications for river basin management. Given the prevalence of organic and particulate P forms in our catchment transect, the bioavailability of these fractions needs to be better understood.     

Distribution of organochlorines in the dissolved and suspended phase of the sea-surface microlayer and seawater in Hong Kong, China

Polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) were measured in the dissolved and suspended particulate phase in the sea-surface microlayer (SML) and subsurface water (SSW) collected from Hong Kong's coastal environment. The concentration ranges (pg/L) for summation sigmaHCHs, summation sigmaDDTs and summation sigmaPCBs in the SSW dissolved phase (DP i.e. sum of truly dissolved and colloidal phase) were 409-940 (mean 602), 774-5583 (mean 1908) and 266-433 (mean 278), respectively. The concentration ranges (pg/L) for summation sigmaHCHs, summation sigmaDDTs and summation sigmaPCBs in SSW suspended particulate matter (SPM) were <5-85 (mean 59), 358-1369 (mean 787) and 85.6-273 (mean 172), respectively. The enrichment factor of PCBs and OCPs in the SML varied between 1.1 and 4.5 for the DP, and 0.4-8.2 for the SPM. The distribution of contaminants between DP and SPM in both the SML and SSW indicates that particulate matter plays an important role in the distribution and fate of DDTs and PCBs, but not for HCH isomers. The Pearl River Estuary is likely to be a major source of contaminants transported to Hong Kong.     

Convection at the melting point: A thermal history of the earth's core

Abstract

Higgins and Kennedy (1971) concluded that the Earth's fluid core has a stable stratification if it is at its melting point. Busse (1972) and Elsasser suggested as an alternative that a hydrostatic-isentropic distribution of particulate solid can produce neutral stability in a partially molten core. Here this suggestion is quantified and a determination is made of the efficiency of the production of fluid motion from the heat flux. This is used to establish that macroscopic convection can exist only if the particulate solid is of sufficiently small size. A thermal history of the core compatible with upper mantle heat flux is advanced in which it is suggested that the inner core is a fairly recent feature. The implication of these results for convection-driven and precession-driven dynamos is that both can function for a small enough suspended particulate, that the convection-dynamo will fail for particles greater than one micron in diameter, and that the precession-driven dynamo probably cannot survive particles greater than ten microns in diameter.     

Carbon and nitrogen cycling in the Zhubi coral reef lagoon of the South China Sea as revealed by 210Po and 210Pb

The radionuclides (210)Po and (210)Pb were examined to trace the cycling of particulate organic carbon (POC) and particulate organic nitrogen (PON) in the Zhubi coral reef lagoon. The net export flux of POC to the open sea is 14 mg Cm(-2) d(-1). However, the net exchange of PON has not yet been observed. On average, the vertical export fluxes in the lagoon of POC and PON, as derived from (210)Po/(210)Pb disequilibria, are 43 mg Cm(-2) d(-1) and 13.8 mg Nm(-2) d(-1), respectively. The deficit of (210)Po relative to (210)Pb in particulate matter provides evidence for the degradation of particulate organic matter. According to the mass balance budgets, 310 mg Cm(-2) d(-1) and 121 mg Nm(-2) d(-1) were recycled into dissolved fractions. Based on a first-order kinetics model, the degradation rate constants of POC and PON are 0.28 and 0.30 m(-1), respectively. Thus, (210)Po and (210)Pb can quantify the cycling of carbon and nitrogen in this coral lagoon.     

Geochemical behavior of 210Pb and 210Po in the nearshore waters off western Taiwan

Dissolved and particulate (210)Pb and (210)Po were determined at 15 stations along the coastline off western Taiwan in April 2007. The (210)Pb activities in dissolved and particulate phases fell within a relatively small range of 2.4-5.2 dpm 100 L(-1) and 1.0-3.2 dpm 100 L(-1), respectively. The dissolved and particulate (210)Po activities also fell within a small range of 0.8-3.4 dpm 100 L(-1) and 1.1-2.9 dpm 100 L(-1), respectively. The correlation of the distribution coefficients (K(d)) of (210)Pb and (210)Po with particle concentration in turbid waters are not as evident as in the open ocean. The mass balance calculation shows that the residence times of (210)Pb and (210)Po with respect to particle removal from the nearshore waters ranges from 3 to 15 days and from 14 to 125 days, respectively. The flux of particulate organic carbon was estimated by (210)Po proxy and ranged from 4.8 to 33.7 mmol-C m(-2) d(-1).     

Manganese oxidation in pH and O2 microenvironments produced by phytoplankton

Pure cultures of Chlorella sp. catalyzed the oxidation of soluble Mn(II) to particulate, extracellular, manganic oxides. Manganese oxidation was dependent on photosynthetic activity: no oxidation was observed in the dark when cells were grown heterotrophically on glucose, or in the light when photosystem II was inhibited by the addition of DCMU. Manganates were not formed when media were buffered below pH 8.0, suggesting that an important driving force for manganese oxidation was the high pH resulting from photosynthesis. Field studies with minielectrodes in Oneida Lake, New York, demonstrated steep gradients of O2 and pH and the presence of particulate manganic oxides associated with pelagic aggregates of the cyanobacterium Microcystis sp. The manganese oxidation reaction apparently occurs only when photosynthesizing algae are present as dense populations that can generate microenvironments of high (>9.0) pH, either as aggregates in the pelagic zone or concentrated cell cultures in the laboratory. A large-scale transition from soluble to particulate manganese was measured in the surface waters of Oneida Lake throughout summer 1986. Removal of Mn(II) was correlated with the presence of aggregate-forming cyanobacteria that oxidize Mn(II) by the mechanism described above.     

Dynamics of particulate major and trace elements in the lower reaches of the Daugava River and adjacent area of the Gulf of Riga (Baltic Sea)

Suspended particulate matter (SPM) was collected in the freshwater-seawater mixing zone in the lower reaches of the Daugava River (Latvia) and adjacent marine area, during five cruises in 1998-2001. The study focused on biogeochemical phase exchange processes. SPM in the freshwater was found to be mainly allochthonous with a high content of organic matter, Mn and sorbed phosphate. Property-salinity plots suggested flocculation of humic-Fe complexes across the salinity gradient. The variability of sorbed phosphate was related to particulate Fe, although no dependence on pH and ionic strength was observed. The Mn contents of SPM mainly follow conservative mixing, but there are also indications of interface exchange of Mn in the mixing zone. The geochemical behaviour of particulate Al appears to differ from that of Fe. In early spring, trace element contents in SPM (Cr, Ni, Cu, Zn, Cd, Pb) correlate tightly with particulate organic matter, whose distribution is linked to phytoplankton distributions.     

Seasonal variations in the cycling of aluminium,cadmium and manganese in a Scottish sea loch: biogeochemical processes involving suspended particles

Concentrations of Al, Cd and Mn were determined in water and particles collected from water bottles over one year during 19 surveys of a silled fjord. Nutrient and hydrographic data were also collected. Particle fluxes were determined at one site using a sediment trap array. Concentrations of dissolved Al showed the strongest (negative) relationship to salinity (r=0.91). This correlation decreased with the onset of the diatom bloom and was insignificant immediately post bloom. Removal of dissolved Al was coincident with an increase in particulate Al concentrations. The degree of removal could be predicted from previously reported Al/Si uptake ratios. Concentrations of leachable P in particulate material from the sediment traps increase at the onset of the bloom and decrease coincident with rapid regeneration as the bloom crashed. Particulate leachable Cd showed a lag in apparent uptake and regeneration relative to particulate leachable P. A substantial amount (ca. 53%) of the annual particle flux of Mn to the deepest trap is material recycled at the sediment surface and is not accumulated in the bottom sediment. Dissolved and particulate Mn levels in the loch have a strong seasonal pattern with low values prior to the spring phytoplankton bloom and increased values after the bloom crash. Maximum concentrations were observed in late autumn. Levels decreased to near pre-bloom values early the following year. This suggests bacterial decay of deposited organic carbon associated with the spring bloom-maintained suboxic conditions at or near the seawater-sediment interface throughout the majority of the year. After exhaustion of this organic matter pool recycling ceased for a brief (2–3 months) winter period.     

Concentrations and transport of trace metals in the St. Lawrence River

Samples of raw water were collected in the St. Lawrence River during six sampling trips from August 1990 to April 1992. Water samples were analyzed for both dissolved and particulate phases for five trace metals. Partition coefficients (Kd) and metal fluxes were calculated in order to determine metal transport. A mass balance equation was used for the determination of the major metal sources to the St. Lawrence River and an estimation of metal loadings to the estuary was made. Average dissolved metal concentrations were found to be Cd 10 ng/L, Co 74 ng/L, Cu 64 ng/L, Fe 69 µg/L and Mn 700 ng/L. Particulate concentrations were (in µg/g) 1.68 for Cd, 31 for Co, 73 for Cu, 25 mg/g for Fe and 1.69 mg/g for Mn. Co, Fe and Mn were transported essentially in the particulate phase while Cd and Cu were predominantly found in the dissolved phase at 56% and 48% of the total metal concentration respectively. Log Kd values varied from 5.1 (for Cu) to 6.8 (for Mn). In the dissolved phase the major sources were found to be the Great Lakes and the Ottawa River whereas in the particulate phase Québec tributaries appear to be the most important. Industrial inputs are quite important in both the dissolved and the particulate phases for Cd, whereas other sources are very variable, especially for the dissolved phase.     

Forecasting Air Quality Indicators for 33 Cities in China

The Jing‐Jin‐Ji (Beijing‐Tianjin‐Hebei) and the surrounding Jin‐Lu‐Yu (Shanxi‐Shandong‐Henan) regions are experiencing severe problems with air pollution. To measure the change in pollutant concentrations over the next few years, the fractional order accumulation grey model is used to forecast the air quality indicators. The results show that the concentrations of fine particulate matter, particulate matter 10, and sulfur dioxide show a downward trend, and 8‐h O₃ (annual) and 8‐h O₃ (spring and summer) show an upward trend in these areas. There is a slight increase in nitrogen dioxide concentration in Shanxi, but its concentration in other areas shows a slight decline. The results obtained can provide a clear direction for air quality management decisions.