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The study of the effect of pH on phosphate sorption by different trophic lake sediments.

This paper studies the effect of pH on phosphate sorption by the sediments of different trophic lakes, including sorption isotherms with different pH values, their effect on sorption rate, their impact on the kinetics of sorption and desorption. The following conclusions are drawn. (1) The phosphate sorption capacity of lake sediment is correlated with pH, but not with its trophic level; that is, pH at 7.0>5.5>9.0. The three isotherms models cannot well describe phosphate sorption by different trophic sediments with different pH, and its applicability seems irregular. (2) The power function equation is one of the best kinetic models, which can provide satisfactory fitting of the kinetic data of phosphate sorption by different trophic sediments, and there is no obvious difference between them. The quick phosphate sorption by the sediment takes place mainly at 0-0.5 h, the pH value has a remarkable effect on the rate of phosphate sorption by the sediment, and sediments in different trophic states tend to have similar trends of change, with pH 5.5>7.0>9.0. (3) The effect of pH on phosphate sorption shows a similar trend for different trophic sediments; namely, as pH increases phosphate sorption rate tends to increases sharply at first and then drop suddenly. After a while it increases slightly, and finally a slight decrease follows as the pH increases. The maximum and minimum of phosphate sorption capacity may be attributed to the rate of phosphate release. (4) Phosphate sorption by lake sediments is not completely reversible and strong bonding occurs between sediment particles and sorbed phosphate. This makes it difficult for the sorbed phosphate to be desorbed from the sediments. The amounts of desorbed phosphate are almost the same in different trophic sediments with different initial pH values; that is, the effect of pH on phosphate desorption is small.

Fresh Water↗

The effects of sediment size fraction and associated algal biofilms on the kinetics of phosphorus release.

Experiments using flumes containing sediment of three different size fractions, from two sites on the River Tame, investigated the influences of sediment particle size, and an associated biofilm, on sediment-water exchanges in heterogeneous sediment deposits. This is the first study undertaken to understand the kinetics of the release of soluble reactive phosphorus from sediments of natural systems to identify which of the size compartments affected those fluxes most. Samples of fine material (<2 mm), gravel (2-20 mm), and stones (>20 mm) were collected over a period of several weeks and brought to a fluvarium where they were placed in artificial, controlled flow, and flume channels. Synthetic solutions of similar ionic strength to the river were prepared using calcium chloride. Temperature, pH, and dissolved oxygen of the solution overlying the sediment were monitored automatically whilst filtered samples were obtained at 2 h intervals over 48 h. The biomass, expressed as mg m(-2) chlorophyll a, of the algal component of the biofilm from the surface of the sediment was estimated using methanol extraction. Differences in the responses were observed between the sediment size fractions and the two sites, where contaminant concentrations varied. The equilibrium phosphate concentration and a phosphorus transfer index were used to establish that there was a net uptake of phosphorus by all three sediment size fractions, from both sites, at the time of sampling. The kinetic results showed very fast initial reactions of phosphorus release from the larger size fractions with a well-developed filamentous algal growth present implying a different mechanism than diffusion being involved. The stones and associated biofilms also released more phosphorus than the fine fraction, e.g. final release concentrations for the most contaminated site were: fines approximately 2.5 microM, gravel approximately 6.5 microM, and stones approximately 65.0 microM (expressed as soluble reactive phosphorus). Phosphorus fluxes, calculated assuming the concentration of phosphorus in the sediment was less than the equilibrium concentration, were a maximum at the most contaminated site, e.g. fines 6.4 nmol m(-2) s(-1), gravel 27 nmol m(-2) s(-1), and stones 109 nmol m(-2) s(-1) (normalised with respect to the river bed area). These results confirm that sediment having a biofilm and associated particulate material results in a greater flux than fine sediment, which does not support a filamentous biomass. Removal of the fine particulates trapped in the algal growth reduced soluble phosphorus release. These factors demonstrate that both gravel and stone substrates have an important control over the release of soluble reactive phosphorus.

Biofilms↗

Manmade and natural radionuclides in north east Atlantic shelf and slope sediments: Implications for rates of sedimentary processes and for contaminant dispersion.

Results are presented for a study of manmade and natural radionuclides in north east Atlantic continental shelf and slope sediments to the west of Scotland. The data are interpreted in the context of sediment mixing and accumulation processes and are used to establish the westward extent of contamination of the sediment system. Offshore shelf and slope sediments were found to have post-glacial sedimentation rates of the order of 1 cm ky(-1) but nearshore sediments had much higher accumulation rates of the order of 0.1 cm y(-1). Surface mixed layer depths of up to 6 cm were observed and non-local mixing affected most of the slope sediments, resulting in advective transport of surface sediment to depths of up to 10 cm. Biodiffusion coefficients for offshore shelf and slope sediments were dominantly in the range 10(-8) to 10(-9) cm2 s(-1). The study confirmed that seawater contaminated with Sellafield waste radionuclides is dominantly entrained to the east of 7 degrees W and, consistent with this, higher levels of Sellafield derived radionuclides were confined to nearshore sediments, with lower levels to the west of 7 degrees W. 238Pu/(239,240)Pu data indicated that Sellafield contributed 75-91% of the total plutonium in coastal sediment but only about 4-8% of the total in slope sediments. By analogy, it can be concluded that a similar situation will apply to other contaminants in seawater entering the north east Atlantic via the North Channel.

Atlantic Ocean↗

Biogeochemical conditions in sediments enriched by organic matter from net-pen fish farms in the Bolinao area, Philippines.

Sedimentation and sediment metabolism was measured at eight active milkfish fish pens and at one abandoned site in the Bolinao area, Philippines in order to examine the interactions between sediment and water in this shallow coastal zone. The rates of sedimentation were high in the area due to siltation, but the activities in the fish pens also contributed to enhanced sedimentation as indicated by the difference between the abandoned and active sites. The sediment metabolism appeared to decrease with increasing rates of sedimentation indicating that the microbial activity reached a saturation level in the fish pen sediments. Anaerobic processes dominated the organic matter decomposition, and sulfate reduction rates are among the highest measured in fish farm sediments. The rates decreased with increasing organic loading despite high concentrations of sulfate (>10 mM) at all sites. Presence of methane bubbles in the sediments suggests that sulfate reduction and methanogenesis were coexisting. The sediment metabolism was significantly reduced at the abandoned site indicating that the stimulation of microbial activities is due to active fish production. The anaerobic activity remained high at the abandoned site indicating that the sediment biogeochemical conditions remain affected long time after fish production has ceased.

Anaerobiosis↗

Microbial PCB dechlorination in dredged sediments and the effect of moisture.

Evidence of reductive dechlorination of polychlorinated biphenyls (PCBs) in sediments was investigated in Hudson River sediments dredged and encapsulated in 1978 at Moreau, NY. The effect of different moisture contents in dredged sediments on dechlorination and dechlorinating microorganisms was also determined using PCB-spiked sediments in which the moisture level was adjusted by simulating a dewatering process. The congener pattern of PCBs indicated that the dechlorination in the dredged sediments was far less advanced than that in the river sediments collected from the general area of the dredged site (Ft. Edward site). Dechlorination in encapsulated sediments at the Moreau site appeared to have stopped soon after dredging. When microorganisms eluted from the encapsulated sediments were inoculated in clean sediments spiked with Aroclor 1242, an extensive dechlorination was observed, indicating that the encapsulated sediments still harbored dechlorinating microorganisms. However, the same inoculum failed to further dechlorinate residual congeners in the dredged sediments. On the other hand, an inoculum obtained in 1990 from the dredged site in the Hudson River dechlorinated the residual congeners further. In simulated dredged sediments, the maximum level of dechlorination was lower at reduced moisture contents. The population size of dechlorinating microorganisms, as determined by the most probable number (MPN) technique, was also smaller at the lower moisture levels. There was a significant correlation between the maximum extent of dechlorination and the specific death rate of dechlorinating populations. These results indicate that the underlying mechanism of the moisture-dependent maximum dechlorination is the moisture-dependence of the death rate of dechlorinating microorganisms.

Biodegradation, Environmental↗

Chemical and bacterial changes during laboratory conditioning of formulated and natural sediments.

Within the framework of toxicity testing using formulated sediment, a conditioning treatment prior to toxic contamination has been examined. This preliminary step enables the bacterial colonisation of the sediment, the initiation of organic matter degradation, and the establishment of stable biological and physico-chemical conditions. The treatment involved in keeping the formulated sediment under water in conditions similar to that chosen for toxicity tests. The behaviour of a formulated sediment was compared with a natural sediment. The monitoring of physico-chemical and biological parameters of sediment and water column was carried out over a 30-day incubation in two laboratories. The parameters of pH and redox, dissolved organic carbon (DOC), NH4 and NO2, total organic carbon (TOC) were measured. The bacterial community was characterised by the determination of bacterial density, in total bacteria number or colony forming units (CFU), several exoenzymatic activities (P-glucosidase, xylosidase, leucine-amino-peptidase phosphatase and sulfatase activities), and three gas productions (CO2, N2O and CH4). The same experiment was carried out with a natural sediment. A 10- to 15-day conditioning allowed a physico-chemical stabilisation and corresponded to kinetic changes in hydrolysis activities. As compared to data of the natural sediment, the biological activity of the formulated sediment showed a different dynamic with lower activity levels. For both sediments, an important decrease of activities levels was observed after 15 days because of a substrate limitation. The work showed that a preliminary conditioning treatment of a formulated sediment provides the stabilisation of parameters that can affect toxicant bioavailability. Additional research is needed to determine the real influence of conditioning on the bioavailability of contaminants. The possible advisability of organic matter input, to maintain the sediment bacterial activity, has to be studied.

Bacteria↗

Method for enumeration of 5-cyano-2,3-ditoyl tetrazolium chloride (CTC)-active cells and cell-specific CTC activity of benthic bacteria in riverine, estuarine and coastal sediments.

Bacteria are the most abundant and active organisms in marine sediments and are critical for nutrient cycling and as a food source to many benthic and pelagic organisms. Bacteria are found both as free-living cells and as particle-associated cells, which can make investigations of these communities difficult. We found that common procedures for extracting bacteria from sediments leave the bacteria clay particle-associated and the clay particles clump, which reduce the reproducibility of direct counts. We optimized a sonication/surfactant method that produces a homogeneous suspension of bacterial cells against a uniform background of clay particles, which results in reproducible samples for epifluorescence microscopy. We developed a method to estimate CTC-positive cells and cell-specific CTC content in intact cores of surficial sediment communities from riverine, estuarine and coastal sites. Benthic bacterial abundances averaged 4.9x10(8) cells/g dry wt sediments in Apalachicola River, Florida sediments, 4.9-13.8x10(9) cells/g dry wt sediments in a variety of Apalachicola Bay sediments and 3.6x10(8) cells/g dry weight in shallow, anoxic Gulf of Mexico sediments. Percent CTC-positive cells ranged from low values of 9-10% CTC-positive cells in Apalachicola River and Apalachicola Bay sediments to high values of 25% CTC-positive cells in anoxic Gulf of Mexico sediments. After correction for abiotic CTC reduction and chlorophyll interference, estimates of cell-specific CTC reduction ranged from 0.15 to 0.55 fmol CTC(red)/active cell in the Apalachicola Bay sediments to 1.6 to 3.8 fmol CTC(red)/active cell in anoxic Gulf of Mexico sediments.

Bacteria↗

Diffusion of the synthetic pyrethroid permethrin into bed-sediments.

Bed-sediments are a sink for many micro-organic contaminants in aquatic environments. The impact of toxic contaminants on benthic fauna often depends on their spatial distribution, and the fate of the parent compounds and their metabolites. The distribution of a synthetic pyrethroid, permethrin, a compound known to be toxic to aquatic invertebrates, was studied using river bed-sediments in lotic flume channels. trans/cis-Permethrin diagnostic ratios were used to quantify the photoisomerization of the trans isomer in water. Rates were affected by the presence of sediment particles and colloids when compared to distilled water alone. Two experiments in dark/light conditions with replicate channels were undertaken using natural sediment, previously contaminated with permethrin, to examine the effect of the growth of an algal biofilm at the sediment-water interface on diffusive fluxes of permethrin into the sediment. After 42 days, the bulk water was removed, allowing a fine sectioning of the sediment bed (i.e., every mm down to 5 mm and then 5-10 mm, then every 10 mm down to 50 mm). Permethrin was detected in all cases down to a depth of 5-10 mm, in agreement with estimates by the Millington and Quirk model, and measurements of concentrations in pore water produced a distribution coefficient (Kd) for each section. High Kd's were observed for the top layers, mainly as a result of high organic matter and specific surface area. Concentrations in the algal biofilm measured at the end of the experiment under light conditions, and increases in concentration in the top 1 mm of the sediment, demonstrated that algal/ bacterial biofilm material was responsible for high Kd's at the sediment surface, and for the retardation of permethrin diffusion. This specific partition of permethrin to fine sediment particles and algae may enhance its threat to benthic invertebrates. In addition,the analysis of trans/cis-permethrin isomer ratios in sediment showed greater losses of trans-permethrin in the experiment under light conditions, which may have also resulted from enhanced biological activity at the sediment surface.

Bacteria↗

PCBs and OCPs in sediment cores from the Lower St. Lawrence Estuary, Canada: evidence of fluvial inputs and time lag in delivery to coring sites.

Three sediment cores were collected along the longitudinal axis of the Laurentian Trough in the Lower St. Lawrence Estuary (LSLE) and an additional one at the junction of the Estuary and the Gulf of St. Lawrence. After core-slicing, each sediment layer was analyzed for polychlorinated biphenyls (PCBs) and some organochlorine pesticides (OCPs) including p,p'-dichlorodiphenyltrichloroethane (DDT) and its metabolites, hexachlorobenzene (HCB) and Mirex. 210Pb activity was also measured in these sediments, which allowed us to confirm that these cores were too much affected by the overall impact of surface mixing to be dated. Nevertheless, POP sedimentary profiles in cores from the LSLE upstream stations showed well-defined subsurface peak concentrations. Apparently, the peak inputs of POPs to these sediment cores had occurred after the years of maximum sales and production of these chemicals in North America, suggesting a time lag in the delivery of POPs to the LSLE sediments. Concentrations of POPs in the LSLE surface sediments as well as POP inventories in sediment cores decreased in the seaward direction, confirming that the head of the LSLE acts as a sink for sediments and associated constituents. Surface concentrations of sigmaPCBs, sigmaDDTs, and HCB in the most upstream core were on average similar to those reported in two fluvial lakes of the St. Lawrence River but were between 12 and 39 times lower than those from Lake Ontario. For Mirex, the surface concentration in that core was 5 and 130 times lower than the average values found in the fluvial lakes and Lake Ontario, respectively. Differences between Lake Ontario sediment cores and the most upstream core from the LSLE were much smaller on the basis of POP inventories than surface concentrations of POPs, but were still important. The total burdens of POPs in LSLE sediments below the 200 m isobath were 8704 kg for sigmaPCBs, 1825 kg for sigmaDDTs, 319 kg for HCB, and 27.5 kg for Mirex. These values represent between 1% and 10% of the total burdens of these POPs in Lake Ontario sediments. The estimated contribution of POPs by direct atmospheric deposition into the water column area of the LSLE represented at most 30% of the total sediment burdens of POPs in the LSLE, illustrating the importance of fluvial inputs.

Canada↗

Release of atrazine ((14)C) from two undisturbed submerged sediments over a two-year period.

Through water erosion and runoff, sediment-adsorbed atrazine can undergo sedimentation and accumulation at the bottom of water bodies and become potential sources of atrazine to the water column. The purpose of this study is to determine the fate and release of atrazine ((14)C) to the water column from two simulated undisturbed submerged sediments at two temperature treatments (5 and 24 degrees C) over a 2-year period. Atrazine residue ((14)C) was released from the two sediments and was, primarily, diffusing from the sediment pore water to the water columns. The amount released was affected by sediment type and is related to the sediment's adsorption/desorption capacity. Larger amounts of residue ((14)C) were released to the water columns at 5 degrees C than at 24 degrees C. Atrazine degraded in the shallow submerged anaerobic sediment's water columns over the 2-year period. Less than 2% (percent of applied in atrazine equivalent) of extractable atrazine and metabolites remained in the sediment after 2 years. The amount of nonextractable atrazine residue ((1)(4)C) was significantly higher in sediments at 24 degrees C than at 5 degrees C. In conclusion, atrazine accumulating in shallow undisturbed submerged sediments from nonpoint sources would most likely degrade and/or become nonextractable over time and would have a low probability of becoming a significant source to the water body. The conditions where accumulation and future release of atrazine have a greater potential to occur are under very cold temperatures with low adsorption capacity sediments.

Atrazine↗

The clinical use of erythrocyte sedimentation rate in pyogenic vertebral osteomyelitis.

STUDY DESIGN: Retrospective chart review of 44 cases. OBJECTIVE: To describe the clinical usage of the erythrocyte sedimentation rate in pyogenic vertebral osteomyelitis. SUMMARY OF BACKGROUND DATA: The erythrocyte sedimentation rate is often used to determine the efficacy and duration of treatment in pyogenic vertebral osteomyelitis. Although consensus and anecdotal reports support this notion, no detailed review of the erythrocyte sedimentation rate response in conservative treatment of pyogenic vertebral osteomyelitis has been made, to date. METHODS: For 44 patients with pyogenic vertebral osteomyelitis who had erythrocyte sedimentation rate testing at or before the time of diagnosis and at least twice during the next month, the clinical findings and results of the erythrocyte sedimentation rate testing were reviewed. RESULTS: Of 18 cases with no significant fall in the erythrocyte sedimentation rate during the first month, 9 (50%) failed conservative treatment. Conversely, of the 26 cases with a good erythrocyte sedimentation rate response during the first month, three (12%) were clinical failures. However, a rapid decline of the erythrocyte sedimentation rate (> 50% in the first month) is rarely seen in treatment failure. In addition, approximately 2 weeks after antibiotic treatment, 19 of 32 were actually higher than at the time of diagnosis, but went on to clinical cure without surgery. The erythrocyte sedimentation rate, in combination with the patient's age and immune status, predicted the success of antibiotic treatment, in most cases. The erythrocyte sedimentation rate response alone during the first month was not a clear predictor of success. CONCLUSIONS: Although the erythrocyte sedimentation rate does correlate well with response to treatment as a general rule, care must be taken in interpretation of a persistently elevated or even rising erythrocyte sedimentation rate as an isolated clinical finding.

Adolescent↗

Toxicokinetics of sediment-associated polybrominated diphenylethers (flame retardants) in benthic invertebrates (Lumbriculus variegatus, Oligochaeta).

Polybrominated diphenylethers (PBDEs) are ubiquitous environmental contaminants showing rapid temporal increase in some sample types. The compounds are known to biomagnify in aquatic food webs and are assumed to archive into sediments and soils. Currently, no direct evidence indicates whether sediment-associated PBDEs are available for biota. The aim of the present study was to explore the uptake and elimination of two common congeners (47 and 99) in sediment-inhabiting invertebrates to shed light on possible bioavailability of sediment-associated PBDEs. Two clean lake sediments were spiked with environmentally relevant concentrations of 14C-labeled tetra- and pentabromo diphenylether, and oligochaetes (Lumbriculus variegatus) were exposed for three or four weeks to allow kinetic accumulation calculations. Subsequent depuration tests were performed after three weeks of exposure to obtain depuration rates. Both congeners were clearly bioavailable, and only slight differences in steady-state tissue concentrations were found between the four sediment-ingesting oligochaete treatments (biota sediment accumulation factors [BSAFs], 3.0-3.7). The tetrabromo diphenylether-exposed oligochaetes that did not ingest sediment had clearly lower influx rates (0.1 vs 1-3 nmol h(-1)) than sediment-ingesting worms. Also, the estimated BSAF (1.8) was statistically different from that of the sediment-ingesting oligochaetes. These findings support the significance of feeding behavior in bioaccumulation of very hydrophobic organic contaminants. Depuration of both congeners was biphasic, indicating two kinetically different compartments in L. variegatus. Compartment A made up 73 to 92% of total radioactivity in tissues and had relatively fast depuration rates (half-lives, 10.5-47.5 h); the smaller compartment B had very slow depuration rates. No significant biotransformation of PBDEs was evident. The present study clearly demonstrates that the sediment-associated PBDEs, like other hydrophobic organic contaminants of environmental concern, are not totally sequestered from sediment-inhabiting oligochaetes and are subject to trophic transfer.

Animals↗

Solid-phase microextraction for predicting the bioavailability of 2,4,6-trinitrotoluene and its primary transformation products in sediment and water.

Disposable solid-phase microextraction fibers (SPMEs) were used to measure the availability of 2,4,6-trinitrotoluene (TNT) and its two primary transformation products, 2-amino-4,6-dinitrotoluene (2ADNT) and 4-amino-2,6-dinitrotoluene (4ADNT). The SPMEs (85-microm polyacrylate) and sediment-dwelling oligochaetes (Tubifex tubifex) were exposed to TNT-spiked sediment, to TNT-spiked sediment amended with activated carbon, and to TNT-, 2ADNT-, and 4ADNT-spiked water. Sediment concentration was a poor predictor of bioavailability in unamended and carbon-amended sediments (r2 = 0.14-0.73) The activated carbon amendment reduced the bioavailability of compounds in carbon-amended sediment, causing the relationships between Tubifex concentrations and sediment concentrations to differ significantly between unamended and carbon-amended sediment for all compounds. In contrast, SPME TNT concentrations predicted Tubifex TNT concentrations (r2 = 0.54-0.79). and regression models did not differ significantly among the three TNT-spiked matrices. The SPME 2ADNT and 4ADNT concentrations also were predictive of Tubifex 2ADNT and 4ADNT concentrations (r2 = 0.44-0.90). Relationships between Tubifex concentrations and SPME concentrations were the same between unamended and carbon-amended TNT-spiked sediments for 2ADNT and 4ADNT; however, the relationship in sediment (pooled data) differed from the relationship found in 2ADNT- and 4-ADNT-spiked water. The SPMEs provided carbon amendment-independent measures of ADNT availability in sediment and matrix-independent measures of TNT availability among the three matrices. The SPMEs show promise for predicting bioavailable organic compounds in sediment and water.

Animals↗

Regional scale variability in sediment and nutrient delivery from small agricultural watersheds.

Although many studies have pointed out the various controlling factors of sediment and nutrient delivery on a plot or watershed scale, little is known on the spatial variability of sediment and nutrient delivery on a regional scale. This study was conducted to reveal regional variations in sediment-associated nutrient delivery in central Belgium. Sediment deposited in 13 small retention ponds was sampled and analyzed for total phosphorus (TP), K, Mg, and Ca content. The TP content of the sediment deposits varied from 510 to 2001 mg P per kg sediment. Nutrients are predominantly fixed on the very fine sediment fraction (<16 microm), which is the reason why the nutrient trap efficiency of the ponds is only a fraction of the sediment trap efficiency. Average nutrient trap efficiency of the studied ponds varies between 4 and 31%, whereas sediment trap efficiency varies between 10 and 72%. For watersheds ranging from 7 to 4873 ha, sediment yield ranged between 1.2 and 20.6 Mg ha(-1) yr(-1), whereas TP export varied from 1.8 to 39.7 kg ha(-1) yr(-1). The observed spatial variability in nutrient losses is primarily attributed to regional variations in erosion and sediment yield values and to a far lesser degree to the spatial variations in fertilizer application. Redistribution of manure in the framework of an agricultural policy may increase the rate of nutrient delivery by ways of erosion and sediment transport.

Agriculture↗

Temporal and spatial distributions of sediment total organic carbon in an estuary river.

Understanding temporal and spatial distributions of naturally occurring total organic carbon (TOC) in sediments is critical because TOC is an important feature of surface water quality. This study investigated temporal and spatial distributions of sediment TOC and its relationships to sediment contaminants in the Cedar and Ortega Rivers, Florida, USA, using three-dimensional kriging analysis and field measurement. Analysis of field data showed that large temporal changes in sediment TOC concentrations occurred in the rivers, which reflected changes in the characteristics and magnitude of inputs into the rivers during approximately the last 100 yr. The average concentration of TOC in sediments from the Cedar and Ortega Rivers was 12.7% with a maximum of 22.6% and a minimum of 2.3%. In general, more TOC accumulated at the upper 1.0 m of the sediment in the southern part of the Ortega River although the TOC sedimentation varied with locations and depths. In contrast, high concentrations of sediment contaminants, that is, total polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs), were found in sediments from the Cedar River. There was no correlation between TOC and PAHs or PCBs in these river sediments. This finding is in contradiction to some other studies which reported that the sorption of hydrocarbons is highly related to the organic matter content of sediments. This discrepancy occurred because of the differences in TOC and hydrocarbon source input locations. It was found that more TOC loaded into the southern part of the Ortega River, while almost all of the hydrocarbons entered into the Cedar River. This study suggested that the locations of their input sources as well as the land use patterns should also be considered when relating hydrocarbons to sediment TOC.

Carbon↗

Effect of sediment toxicity on anaerobic microbial metabolism.

Mineralization of a readily biodegradable aromatic compound (benzoate) by intrinsic microorganisms in the anoxic sediment was used to quantify the inhibitory effect of heavily contaminated sediment from the Arthur Kill estuary (NY/NJ Harbor system, USA) on the anaerobic metabolism by naturally present bacterial populations. In anoxic microcosms, the effect of varying ratios of contaminated sediment:site water and contaminated sediment:noncontaminated sediment (Flax Pond, Stony Brook, NY, USA) were investigated. In all cases, increasing the ratio of Arthur Kill sediment in the microcosms showed an inhibitory effect on the rate of 14C-benzoate mineralization as measured by the evolution of 14CO2. This inhibitory effect could be alleviated through dilution of the sediment with noncontaminated sediment, resulting in some cases in mineralization rates that were greater by an order of magnitude. The toxicity of the sediment was confirmed by whole-sediment Microtox bioassay. Analysis of the sediment revealed high (>200 mg/kg) levels of Pb, Cu, Zn, and Cr, suggesting that heavy metals may contribute to overall sediment toxicity.

Bacteria, Anaerobic↗

Polychlorinated dibenzo-p-dioxins and dibenzofurans and dioxinlike polychlorinated biphenyls in sediments and mussels at three sites in the lower Great Lakes, North America.

Levels of contaminants including polychlorinated dibenzo-p-dioxins (PCDDs), polychlorinated dibenzofurans (PCDFs), non-ortho-substituted and mono-ortho-substituted dioxinlike polychlorinated biphenyls (DLPCBs) were determined in sediments and freshwater mussels (Dreissena spp. and Elliptio complanata) at three sites in the lower Great Lakes (North America). Impacts of mussel colonization on sediment quality were investigated by comparing contaminant levels in colonized sediment with levels in sediment in the same area that was not colonized, but exposed to similar environmental conditions. Significant impacts on contaminant levels of colonized sediment, compared to noncolonized sediment, were observed at two sites exhibiting high mussel population densities (Fort Erie, eastern Lake Erie, ON, Canada, 2.2 kg/m2 dry wt biomass, and Port Dalhousie, western Lake Ontario, Ontario, Canada, 6.1 kg/m2 dry wt biomass); these differences were not observed at a site with lower mussel densities (Bay of Quinte, eastern Lake Ontario, Ontario, Canada, 0.7 kg/m2). Total organic carbon and contaminant concentrations were statistically significantly greater in colonized sediment, compared to noncolonized sediment, at the two impacted sites. Areal estimates of PCDD/PCDF and DLPCB toxicity equivalents (TEQs) in mussel biomass at the three sites averaged 0.16% and 3.3%, respectively, of the TEQs in the top 3 cm of sediment, indicating that the sediments were the primary sink for contaminants. The observed differences between colonized and noncolonized sediment suggest that Dreissena are capable of influencing the chemical properties of sediment they colonize.

Animals↗

Correlations of extractable heavy metals with organic matters in contaminated river sediments.

In southern Taiwan, almost all the main rivers have been contaminated by anthropogenic heavy metals and organic matters. The main pollution sources include agricultural, industrial, and domestic activities. River sediments potentially have large capacities to accumulate heavy metals and organic matters when the river water flows through it. The sediments sampled from high contaminated river (the Yenshui River) and moderately contaminated rivers (the Tsengwen, Chishui, Potzu, and Peikang Rivers) were used to realize correlations between each kind of aqua regia extractable heavy metals (Co, Cr, Cu, Zn, Ni, Pb, Mn, and Fe) and organic matters in vertical sediment cores. Organic matters and aqua regia extractable heavy metal concentrations, analyzed by strong acid-digested extraction, were determined in vertical profile segments from downstream sediments of the five rivers. Sum of six aqua regia extractable heavy metals (Co, Cr, Cu, Zn, Ni, and Pb) were below 3,000 mg/kg in sediments of the Yenshui River, and below 500 mg/kg in the other four rivers' sediments. Strongly positive correlations (r = 0.83-0.95) between each kind of aqua regia extractable heavy metals and organic matters (concentration range between 0.6 to 3.8%) were observed in sediments of the Yenshui River. The slopes of the linear regressive lines approximated the average metal complexation ratios with organic matters in the sediments. In sediments of the other four rivers, smaller positive correlation coefficients between aqua regia extractable heavy metals and organic matters (below 2.6%) were observed. The complexation ratios derived from the four moderately polluted river sediments were smaller than those derived from the highly contaminated river sediments, indicating that the importance of organic matters in the accumulation of heavy metals in river sediments.

Environmental Monitoring↗