Acid Volatile Sulfides and Simultaneously Extracted Metals in a Metal-Polluted Area of Taihu Lake,China

There were similar distribution characteristics for acid volatile sulfides (AVS) and simultaneously extracted metals (SEM) in surface sediments, and the concentrations of AVS and SEM decreased from the deposition area to the center of the bay (lake). The ratio of AVS to SEM was <1 in the surface sediments, indicating that heavy metals in surface sediments may be bioavailable. The concentration of AVS increased with sediment depth, followed by a decrease with large variation, while the concentration of SEM remained constant. By comparing the concentration of SEM with total metals, it was shown that extracted Cu and Ni decreased with sediment depth, indicating increasing association of Cu and Ni with sulfides in deeper sediment layers. The lower extracted ratios for Pb and Zn compared with sulfidic sediment illustrated that AVS should not have strong control on sediment Pb and Zn. The molar ratio of AVS and reactive iron showed that heavy metals were dynamic and active in sediments in this lake.     

Spatial variation of metals and acid volatile sulfide in floodplain lake sediment

In risk assessment of aquatic sediments, much attention is paid to the immobilizing effect of acid volatile sulfide (AVS) on trace metals. The difference of AVS and simultaneously extracted metals (SEM) gives an indication of metal availability. In floodplain sediments, where changing redox conditions occur, AVS may play a major role in determining variation in metal availability. The importance of spatial heterogeneity has been recognized in risk assessment of trace-metal-polluted sediments. However, little is known about spatial variation of available metal fractions. We studied spatial variability of sediment, environmental conditions, total contaminant concentrations, and available metals (as SEM-AVS or SEM-AVS/f(oc)) in a floodplain lake. The top 5 cm of sediment was sampled at 43 locations. Data were analyzed with correlation and principal component analysis as well as with geostatistical methods. Trace metal and SEM concentrations and most sediment characteristics were more or less constant within 10%. In contrast, AVS concentrations were much more variable and showed a strong spatial dependence due to differences in lake depth, total sulfur pools, and redox potential (E(h)), which resulted in crucial differences in trace-metal availability within the lake. The spatial pattern of SEM-AVS deviates from total or normalized trace-metal patterns. This particularly has implications for risk assessment of sediments prone to dynamic hydrological conditions, where AVS concentrations are also variable in time.     

Trace metal availability and effects on benthic community structure in floodplain lakes

Effects of contaminants on communities are difficult to assess and poorly understood. We analyzed in situ effects of trace metals and common environmental variables on benthic macroinvertebrate communities in floodplain lakes. Alternative measures of trace metal availability were evaluated, including total metals, metals normalized on organic carbon (OC) or clay, simultaneously extracted metals (SEM), combinations of SEM and acid-volatile sulfide (AVS), and metals accumulated by detritivore invertebrates (Oligochaeta). Accumulated metal concentrations correlated positively with sediment trace metals and negatively with surface water dissolved OC. Sixty-eight percent of the variation in benthic community composition was explained by a combination of 11 environmental variables, including sediment, water, and morphological characteristics with trace metals. Metals explained 2 to 6% of the community composition when SEM-AVS or individual SEM concentrations were regarded. In contrast, total, normalized, and accumulated metals were not significantly linked to community composition. We conclude that examination of SEM or SEM - AVS concentrations is useful for risk assessment of trace metals on the community level.     

Effects of acid-volatile sulfide on metal bioavailability and toxicity to midge (Chironomus tentans) larvae in black shale sediments

Metal bioavailability and toxicity to aquatic organisms are greatly affected by variables such as pH, hardness, organic matter, and sediment acid-volatile sulfide (AVS). Sediment AVS, which reduces metal bioavailability and toxicity by binding and immobilizing metals as insoluble sulfides, has been studied intensely in recent years. Few studies, however, have determined the spatial variability of AVS and its interaction with simultaneously extracted metals (SEM) in sediments containing elevated concentrations of metals resulting from natural geochemical processes, such as weathering of black shales. We collected four sediment samples from each of four headwater bedrock streams in northcentral Arkansa (USA; three black shale-draining streams and one limestone-draining stream). We conducted 10-d acute whole-sediment toxicity tests using the midge Chironomus tentans and performed analyses for AVS, total metals, SEMs, and organic carbon. Most of the sediments from shale-draining streams had similar total metal and SEM concentrations but considerable differences in organic carbon and AVS. Zinc was the leading contributor to the SEM molar sum, averaging between 68 and 74%, whereas lead and cadmium contributed less than 3%. The AVS concentration was very low in all but two samples from one of the shale streams, and the sum of the SEM concentrations was in molar excess of AVS for all shale stream sediments. No significant differences in mean AVS concentrations between sediments collected from shale-draining or limestone-draining sites were noted (p > 0.05). Midge survival and growth in black shale-derived sediments were significantly less (p < 0.001) than that of limestone-derived sediments. On the whole, either SEM alone or SEM-AVS explained the total variation in midge survival and growth about equally well. However, survival and growth were significantly greater (p < 0.05) in the two sediment samples that contained measurable AVS compared with the two sediments from the same stream that contained negligible AVS.     

Biological response to variation of acid-volatile sulfides and metals in field-exposed spiked sediments

Vertical and temporal variations of acid-volatile sulfides (AVS) and simultaneously extracted metals (SEM) in sediment can control biological impacts of metals. To assess the significance of these variations in field sediments, sediments spiked with cadmium, copper, lead, nickel, and zinc were deployed in Narragansett Bay for four months and recolonization by benthic organisms investigated. In surface sediments, concentrations of AVS decreased with time whenever AVS exceeded SEM but remained unchanged when AVS was less than SEM; in subsurface sediments, concentrations increased slightly. Concentrations of total SEM decreased with time only in surface sediments in which SEM exceeded AVS. Metals were not detected in interstitial waters of sediments where AVS exceeded SEM but were significant when SEM exceeded AVS and followed the order of solubilities of their sulfides. Concentrations in interstitial waters decreased with time, but exceeded U.S. Environmental Protection Agency chronic water quality criteria for 56 to 119 d. After 119 d, faunal assemblages in all treatments were similar to controls. Lack of biological response was related to vertical distributions of AVS and SEM. Biological exposure took place in near-surface sediments, where AVS exceeded SEM in even the highest treatments. Therefore, concentrations of metals in interstitial waters were low and consequently biological impacts were undetectable.     

Mid-Term Variation of Vertical Distribution of Acid Volatile Sulphide and Simultaneously Extracted Metals in Sediment Cores From Lake Albufera (Valencia, Spain)

Lake Albufera is one of the most eutrophic bodies of water in Spain due to point and diffuse pollution over past decades, and its sediments are likely to be anoxic because of high organic matter flux. Hence, sulphides can play an important role in limiting the mobility of heavy metals. This study aimed to study the vertical variation of acid volatile sulphide (AVS) and simultaneously extracted metals (SEM) in sediment cores collected from Lake Albufera; other sediment characteristics, such as organic matter, biochemical oxygen, demand or total metals, were also studied. Three sites were selected, and four sampling campaigns were performed to study spatial and temporal variation as well as to obtain information regarding historical variation in the composition of sediments. AVS and SEM were analysed by the purge-and-trap method. The vertical distribution of AVS and SEM varied depending on the sampling site—concentrations of AVS and SEM were higher at sites close to mouths of inflowing channels. A decreasing trend of AVS has been found at these sites over time: In the two first samplings, AVS increased with depth reaching maximum concentrations of 40 and 21 μmol g^?1, but from then on AVS were lower and decreased with depth. SEM decreased with depth from 3 μmol g^?1 in surface layers to approximately 1 μmol g^?1 at deeper segments at these sites. However, the central site was more uniform with respect to depth as well as with time; it presented lower values of SEM and AVS (mean 0.9 and 2.0 μmol g^?1 respectively), and the maximum value of AVS (7 μmol g^?1) was found at the top layer (0–3 cm). According to the (SEM-AVS)/f_OC approach, every site, and throughout the cores, can be classified as containing nontoxic metals because the values were <130 μmol g^?1.     

Characterizing sediment acid volatile sulfide concentrations in European streams

Sediment acid volatile sulfide (AVS) concentrations were measured in wadeable streams of a wide variety of ecoregions of western Europe (84 sites in 10 countries and nine ecoregions) to better understand spatial distribution and ecoregion relationships. Acid volatile sulfide has been shown to be a major factor controlling the bioavailability and toxicity of many common trace metals, such as Cd, Cu, Ni, Pb, and Zn. Sediment characteristics varied widely. The ratio of the sum of the simultaneously extracted metals (SEM) to AVS ranged from 0.03 to 486.59. The sigmaSEM-AVS ranged from -40.02 to 17.71 micromol/g. On a regional scale, sediment characteristics such as dominant parent soil material showed significant trends in AVS distribution and variation by ecoregion. Total Fe and Mn were correlated weakly with SEM concentrations. Three AVS model approaches (i.e., the SEM:AVS ratio, SEM-AVS difference, and carbon normalization) were compared at threshold exceedance levels of SEM/AVS > 9, SEM-AVS > 2, and SEM-AVS/foc > 150 micromol/g organic carbon (OC). Only 4.76% of the sediments exceeded all three AVS thresholds; 22.6% of the sediments exceeded two models; and 13% of the sediments exceeded one model only. Using the SEM:AVS, SEM-AVS, and fraction of organic carbon models, and including site-specific data and regional soil characteristics, ecoregions 1 (Portugal), 3 (Italy), 4 (Switzerland), and 9 (Belgium/Germany) had the highest potential metals toxicity; ecoregions 13 and 8 (Belgium/France) showed the lowest potential toxicity. However, because AVS can vary widely spatially and temporally, these data should not be considered as representative of the sampled ecoregions. The general relationship between AVS levels and sediment characteristics provides some predictive capability for wadeable streams in the European ecoregions.     

Laboratory Toxicity and Benthic Invertebrate Field Colonization of Upper Columbia River Sediments: Finding Adverse Effects Using Multiple Lines of Evidence

From 1930 to 1995, the Upper Columbia River (UCR) of northeast Washington State received approximately 12 million metric tons of smelter slag and associated effluents from a large smelter facility located in Trail, British Columbia, approximately 10 km north of the United States-Canadian border. Studies conducted during the past two decades have demonstrated the presence of toxic concentrations of heavy metals in slag-based sandy sediments, including cadmium, copper, zinc, and lead in the UCR area as well as the downstream reservoir portion of Lake Roosevelt. We conducted standardized whole-sediment toxicity tests with the amphipod Hyalella azteca (28-day) and the midge Chironomus dilutus (10-day) on 11 samples, including both UCR and study-specific reference sediments. Metal concentrations in sediments were modeled for potential toxicity using three approaches: (1) probable effects quotients (PEQs) based on total recoverable metals (TRMs) and simultaneously extracted metals (SEMs); (2) SEMs corrected for acid-volatile sulfides (AVS; i.e., ∑SEM - AVS); and (3) ∑SEM - AVS normalized to the fractional organic carbon (f(oc)) (i.e., ∑SEM - AVS/f(oc)). The most highly metal-contaminated sample (∑PEQ(TRM) = 132; ∑PEQ(SEM) = 54; ∑SEM - AVS = 323; and ∑SEM - AVS/(foc) = 64,600 umol/g) from the UCR was dominated by weathered slag sediment particles and resulted in 80% mortality and 94% decrease in biomass of amphipods; in addition, this sample significantly decreased growth of midge by 10%. The traditional ∑AVS - SEM, uncorrected for organic carbon, was the most accurate approach for estimating the effects of metals in the UCR. Treatment of the toxic slag sediment with 20% Resinex SIR-300 metal-chelating resin significantly decreased the toxicity of the sample. Samples ∑SEM - AVS > 244 was not toxic to amphipods or midge in laboratory testing, indicating that this value may be an approximate threshold for effects in the UCR. In situ benthic invertebrate colonization studies in an experimental pond (8-week duration) indicated that two of the most metal-contaminated UCR sediments (dominated by high levels of sand-sized slag particles) exhibited decreased invertebrate colonization compared with sand-based reference sediments. Field-exposed SIR-300 resin samples also exhibited decreased invertebrate colonization numbers compared with reference materials, which may indicate behavioral avoidance of this material under field conditions. Multiple lines of evidence (analytical chemistry, laboratory toxicity, and field colonization results), along with findings from previous studies, indicate that high metal concentrations associated with slag-enriched sediments in the UCR are likely to adversely impact the growth and survival of native benthic invertebrate communities. Additional laboratory toxicity testing, refinement of the applications of sediment benchmarks for metal toxicity, and in situ benthic invertebrate studies will assist in better defining the spatial extent, temporal variations, and ecological impacts of metal-contaminated sediments in the UCR system.     

Mobility and bioavailability of trace metals in sulfidic coastal sediments

High concentrations of Hg, Cd, Pb, Cu, and Zn were found in the euxinic sediment of the inner archipelago of Stockholm. In the sulfide-rich sediment, they are precipitated as metal sulfides with low dissolving capacity and bioavailability. In two experiments, the significance of acid-volatile sulfide (AVS) and dissolved sulfides for mobility, bioavailability, and toxicity of metals were studied by oxygenation of intact sediment cores. Influence of bioturbating deposit-feeding amphipods, that is, Monoporeia affinis, was examined on studied sediment processes. Results showed a low mobility of most metals except Cd and Zn. Bioturbation did not enhance mobility. Cd and Zn, released from the sediment, were not bioaccumulated in amphipods. In contrast, the less mobile metals Hg and Pb were bioaccumulated. A low toxicity of contaminated sediments, in terms of mortality and embryonic malformations of amphipods, was recorded. Results indicate that Cd, Zn, and Cu are comparatively unavailable after oxygenation of the metal sulfides. Similar results were recorded in contaminated sediments differing in redox potential, AVS, dissolved sulfides, and organic contents, suggesting that other metal ligands, in addition to AVS, are important for metal bioavailability and toxicity in anoxic and suboxic environments.     

Experimental and modeling investigation of metal release from metal-spiked sediments

In sediments that contain iron monosulfide, cadmium, nickel, lead, zinc, and silver(I) form insoluble metal sulfides that lower the metal ion activity in the sediment-pore water system, thereby reducing toxicity. However, metal sulfides are susceptible to oxidation by molecular oxygen resulting in metal solubilization. To better understand the sources and sinks of metal sulfides in sediments, iron monsulfide-rich freshwater sediments were spiked with cadmium, nickel, lead, zinc, or silver(I) and placed into cylindrical cores with an overlying layer of oxygen-saturated water. Measurements of the dissolved metal concentration in the overlying water were made as a function of time and the vertical profiles of acid-volatile sulfide (AVS) and simultaneously extracted metal (SEM) were measured after 150 d. A one-dimensional reactive and transport model has been employed to help elucidate processes controlling the fate of metals in sediments. The model incorporates metal-sulfide formation, metal-sulfide oxidation, and metal partitioning onto sediment organic carbon and iron oxyhydroxide to simulate the vertical transport of metals throughout the sediment core.     

Field validation of sediment zinc toxicity

A field study was conducted to validate concentrations of zinc in freshwater sediments that are tolerated by benthic macroinvertebrate communities and to determine whether a relationship exists with the acid volatile sulfide (AVS)-simultaneously extracted metal (SEM) model. In both the lake and riverine systems, one sediment type was high in AVS and one low in AVS, which resulted in zinc-spiked sediments that ranged from low to high SEM to AVS ratios. The colonization trays were sampled seasonally, ranging from 6 to 37 weeks of exposure, and were evaluated using several appropriate benthic indices. Results of the field evaluations at the four test sites confirmed the validity of the AVS-SEM model, predicting benthic macroinvertebrate effects correctly 92% of the time. In sediments where the SEM to AVS ratio or the AVS and organic (OC)-normalized fractions exceeded 8 and 583 micromol/g of OC, toxicity was observed from the zinc-spiked sediments. Conversely, when the SEM to AVS ratio or OC-normalized AVS fractions were less than 2 or 100 micromol/g of OC, no toxicity was observed. In the range of 148 to 154 micromol/g of OC, toxicity varied in two treatments. Total zinc concentrations in sediments showed no relationship to benthic effects. The most impaired benthic community occurred in the high-gradient stream sediments, which had low OC and AVS concentrations and SEM to AVS ratios of 33 and 44 in the spiked sediments. Five to six benthic metrics were depressed at SEM to AVS ratios of 8.32 and 9.73. The no-observed-effect level appeared to be near a SEM to AVS ratio of 2, with slight to no effects between ratios of 2.34 and 2.94. No sites with ratios of less than 2 showed any adverse effects.     

Importance of equilibration time in the partitioning and toxicity of zinc in spiked sediment bioassays

The influences of spiked Zn concentrations (1-40 micromol/g) and equilibration time (approximately 95 d) on the partitioning of Zn between pore water (PW) and sediment were evaluated with estuarine sediments containing two levels (5 and 15 micromol/g) of acid volatile sulfides (AVS). Their influence on Zn bioavailability was also evaluated by a parallel, 10-d amphipod (Leptocheirus plumulosus) mortality test at 5, 20, and 85 d of equilibration. During the equilibration, AVS increased (up to twofold) with spiked Zn concentration ([Zn]), whereas Zn-simultaneously extracted metals ([SEM]; Zn with AVS) remained relatively constant. Concentrations of Zn in PW decreased most rapidly during the initial 30 d and by 11- to 23-fold during the whole 95-d equilibration period. The apparent partitioning coefficient (Kpw, ratio of [Zn] in SEM to PW) increased by 10- to 20-fold with time and decreased with spiked [Zn] in sediments. The decrease of PW [Zn] could be explained by a combination of changes in AVS and redistribution of Zn into more insoluble phases as the sediment aged. Amphipod mortality decreased significantly with the equilibration time, consistent with decrease in dissolved [Zn]. The median lethal concentration (LC50) value (33 microM) in the second bioassay, conducted after 20 d of equilibration, was twofold the LC50 in the initial bioassay at 5 d of equilibration, probably because of the change of dissolved Zn speciation. Sediment bioassay protocols employing a short equilibration time and high spiked metal concentrations could accentuate partitioning of metals to the dissolved phase and shift the pathway for metal exposure toward the dissolved phase.     

Trace Metal Levels in Chironomid Larvae and Sediments from a Bolivian River: Impact of Mining Activities

The effect of mining activity on metal accumulation in sediments and Chironomidae in a river in Bolivia was assessed. Surficial sediments and midge larvae (Chironomidae, Diptera) were collected at five sampling sites. Concentrations of the trace metals Cd, Cu, Cr, Ni, Pb, and Zn were measured in organisms and sediments by inductively coupled plasma atomic emission spectrometry. Sediments were subjected to two different extraction procedures to identify total trace metals and reducible trace metals. Geochemical characteristics of the sediment were analyzed: total organic carbon (TOC), Fe and Mn oxides, and particle size distribution. To determine the relative importance of the different sediment factors contributing to the variation in metal accumulation by the chironomid larvae, nonlinear regression models were constructed. No increase in metal concentration in sediment could be measured downstream of the mining activity. Larval concentrations, however, increased markedly. Only for zinc and chromium was a significant amount of variation (48 and 73%, respectively) found. The lack of relationship for the other metals probably was due to a unmeasured exposure route, the overlying water.     

A Site-Specific Evaluation of Mercury Toxicity in Sediment

A site-specific evaluation of mercury toxicity was conducted for sediments of the Calcasieu River estuary (Louisiana, USA). Ten-day whole-sediment toxicity tests assessed survival and growth (dry weight) of the amphipods Hyalella azteca and Leptocheirus plumulosus under estuarine conditions (10 ppt salinity). A total of 32 sediment samples were tested for toxicity, including 14 undiluted site sediment samples and 6 sediment dilution series. All sediment samples were analyzed for total mercury and numerous other chemical parameters, including acid volatile sulfide (AVS) and simultaneously extracted metals (SEM). No toxicity attributable to mercury was observed, indicating that a site-specific threshold for total mercury toxicity to amphipods exceeds 4.1 mg/kg dry weight. Site-specific factors that may limit mercury bioavailability and toxicity include relatively high sulfide levels. Additionally, the chemical extractability of mercury in site sediments is low, as indicated by SEM mercury analyses for three sediment samples containing a range of total mercury concentrations. Received: 17 November 1998/Accepted: 7 June 1999     

Biological and Chemical Characterization of Metal Bioavailability in Sediments from Lake Roosevelt,Columbia River,Washington, USA

We studied the bioavailability and toxicity of copper, zinc, arsenic, cadmium, and lead in sediments from Lake Roosevelt (LR), a reservoir on the Columbia River in Washington, USA that receives inputs of metals from an upstream smelter facility. We characterized chronic sediment toxicity, metal bioaccumulation, and metal concentrations in sediment and pore water from eight study sites: one site upstream in the Columbia River, six sites in the reservoir, and a reference site in an uncontaminated tributary. Total recoverable metal concentrations in LR sediments generally decreased from upstream to downstream in the study area, but sediments from two sites in the reservoir had metal concentrations much lower than adjacent reservoir sites and similar to the reference site, apparently due to erosion of uncontaminated bank soils. Concentrations of acid-volatile sulfide in LR sediments were too low to provide strong controls on metal bioavailability, and selective sediment extractions indicated that metals in most LR sediments were primarily associated with iron and manganese oxides. Oligochaetes (Lumbriculus variegatus) accumulated greatest concentrations of copper from the river sediment, and greatest concentrations of arsenic, cadmium, and lead from reservoir sediments. Chronic toxic effects on amphipods (Hyalella azteca; reduced survival) and midge larvae (Chironomus dilutus; reduced growth) in whole-sediment exposures were generally consistent with predictions of metal toxicity based on empirical and equilibrium partitioning-based sediment quality guidelines. Elevated metal concentrations in pore waters of some LR sediments suggested that metals released from iron and manganese oxides under anoxic conditions contributed to metal bioaccumulation and toxicity. Results of both chemical and biological assays indicate that metals in sediments from both riverine and reservoir habitats of Lake Roosevelt are available to benthic invertebrates. These findings will be used as part of an ongoing ecological risk assessment to determine remedial actions for contaminated sediments in Lake Roosevelt.     

Cadmium accumulation by invertebrates living at the sediment-water interface

Benthic animals can take up trace metals both from the sediment compartment in which they burrow and from the water column compartment above their burrows (we define both compartments as containing water and particles). If criteria for the protection of benthic animals are based on metal concentrations in one of these two compartments, then it should first be demonstrated that the majority of the metal taken up by these animals comes from the given compartment. To determine whether benthic animals take up the majority of their cadmium (Cd) from the sediment compartment, we created a Cd gradient in lake sediment and compared Cd accumulation by the invertebrates colonizing these sediments with Cd concentrations in the sediment compartment. On the basis of this relationship and using a bioaccumulation model, we estimate that indigenous benthic invertebrates take up the majority of their Cd from the water column compartment. The results of our experiment are similar to those from a previous study conducted on a different benthic community in a larger lake. Taxa common to both lakes obtained similar proportions of their Cd from the water column compartment, suggesting that Cd accumulation by the same species will be constant across lakes of differing size and chemistry. Our results strengthen the argument that the protection of benthic communities from metal pollution should consider metal in both the water column and sediment compartments. In this regard, the AVS model, which considers only sedimentary metals, was more effective in predicting Cd concentrations in pore waters than those in most animal taxa. We suggest that measurements of vertical chemical heterogeneity in sediments and of animal behavior would aid in predicting the bioaccumulation and effects of sedimentary pollutants.     

Metals in Surface Sediments of Large Shallow Eutrophic Lake Chaohu,China

Metal contents of surface sediments were analyzed temporally and spatially in Lake Chaohu, China. No obvious temporal variations were observed, which probably due to physio- and bio- mixing, e.g. wind and microbes, in this lake. Enrichment factor of some metals were generally greater than 1.0, suggesting significant anthropogenic impact on metal levels. Significantly positive correlations between concentrations of nutrient and metals indicated that the nutrients transported to this lake contributed, to some extent, to the enrichment of metals. The correlation between trace metals concentrations indicated the co-contamination of anthropogenically derived metal enrichment in surface sediment of Lake Chaohu.     

Bioavailability and Toxicity of Heavy Metals in a Heavily Polluted River,in PRD,China

The research is designed to explore the SEM-AVS concept as a tool to assess bioavailability and toxicity of heavy metals in heavily polluted river sediments. The value of AVS and SEM is in a high level and only a few benthic invertebrate are found. Abundance of benthic invertebrate has significant correlation with SEM/AVS (r= -0.913, p<0.01) and SEM-AVS (r= -0.725, p<0.05). The analytical results of MDS (Non-matric Multi-dimensional Scaling) analysis indicate the benthic community structures of seven among nine stations where the SigmaSEM(5)-AVS<0 are similar. The two facts indicate the SEM-AVS concept also is useful to heavily polluted river sediments.     

Bioavailability of metals to the amphipod Monoporeia affinis: interactions with authigenic sulfides in urban brackish-water and freshwater sediments

Could reduced eutrophication be a potential environmental threat because of increased mobility and bioavailability of trace metals? This question was addressed by oxygenating intact sediment cores, varying in redox potential and salinity, in a test system containing the amphipod Monoporeia affinis. Results show a low mobility of metals during oxygenation, and despite high concentrations of metals in sediments, only Pb showed a notable degree of bioaccumulation. Cadmium was bioaccumulated particularly in freshwater sediment, and body burden of Cd was related to salinity, porewater, and sediment concentrations. Despite high sediment and porewater concentrations of Cu and Zn, no relationship was recorded to body burden. For three of four tested metals, Cd, Pb, and Zn, metals in sediment were more important for body burdens in amphipods as compared to metals in porewater. Food, rather than interstitial water, therefore seems to be the main route of metal contaminants to these amphipods. Furthermore, this observed low release of metals from sediments and low body burden significance of porewater metals indicate that ameliorated oxygen conditions in contaminated sediments may be regarded as a minor environmental threat for one of the most important Baltic benthic organisms.     

Toxicity assessment of sediments from the Grand Calumet River and Indiana Harbor Canal in Northwestern Indiana,USA

The objective of this study was to evaluate the toxicity of sediments from the Grand Calumet River and Indiana Harbor Canal located in northwestern Indiana, USA. Toxicity tests used in this assessment included 10-day sediment exposures with the amphipod Hyalella azteca, 31-day sediment exposures with the oligochaete Lumbriculus variegatus, and the Microtox Solid-Phase Sediment Toxicity Test. A total of 30 sampling stations were selected in locations that had limited historic matching toxicity and chemistry data. Toxic effects on amphipod survival were observed in 60% of the samples from the assessment area. Results of a toxicity test with oligochaetes indicated that sediments from the assessment area were too toxic to be used in proposed bioaccumulation testing. Measurement of amphipod length after the 10-day exposures did not provide useful information beyond that provided by the survival endpoint. Seven of the 15 samples that were identified as toxic in the amphipod tests were not identified as toxic in the Microtox test, indicating that the 10-day H. azteca test was more sensitive than the Microtox test. Samples that were toxic tended to have the highest concentrations of metals, polycyclic aromatic hydrocarbons (PAHs), and polychlorinated biphenyls (PCBs). The toxic samples often had an excess of simultaneously extracted metals (SEM) relative to acid volatile sulfide (AVS) and had multiple exceedances of probable effect concentrations (PECs). Metals may have contributed to the toxicity of samples that had both an excess molar concentration of SEM relative to AVS and elevated concentrations of metals in pore water. However, of the samples that had an excess of SEM relative to AVS, only 38% of these samples had elevated concentration of metals in pore water. The lack of correspondence between SEM-AVS and pore water metals indicates that there are variables in addition to AVS controlling the concentrations of metals in pore water. A mean PEC quotient of 3.4 (based on concentrations of metals, PAHs, and PCBs) was exceeded in 33% of the sediment samples and a mean quotient of 0.63 was exceeded in 70% of the thirty sediment samples from the assessment area. A 50% incidence of toxicity has been previously reported in a database for sediment tests with H. azteca at a mean quotient of 3.4 in 10-day exposures and at a mean quotient of 0.63 in 28-day exposures. Among the Indiana Harbor samples, most of the samples with a mean PEC quotient above 0.63 ( i.e., 15 of 21; 71%) and above 3.4 ( i.e., 10 of 10; 100%) were toxic to amphipods. Results of this study and previous studies demonstrate that sediments from this assessment area are among the most contaminated and toxic that have ever been reported.