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1.
Concentration of aliphatic, aromatic, and chlorinated hydrocarbons were determined from 33 surface-sediment samples taken from the Tidal Basin, Washington Ship Channel, and the Anacostia and Potomac rivers in Washington, D.C. In conjunction with these samples, selected storm sewers and outfalls also were sampled to help elucidate general sources of contamination to the area. All of the sediments contained detectable concentrations of aliphatic and aromatic hydrocarbons, DDT (total dichlorodiphenyltrichloroethane), DDE (dichlorodiphenyldichloroethene), DDD (dichlorodiphenyldichloroethane), PCBs (total polychlorinated biphenyls) and total chlordanes (oxy-, α-, and γ-chlordane and cis + trans-nonachlor). Sediment concentrations of most contaminants were highest in the Anacostia River just downstream of the Washington Navy Yard, except for total chlordane, which appeared to have upstream sources in addition to storm and combined sewer runoff. This area has the highest number of storm and combined sewer outfalls in the river. Potomac River stations had lower concentrations than other stations. Total hydrocarbons (THC), normalized to the fine-grain fraction (clay + silt, < 63 μm), ranged from 120 μg g?1 to, 1,900 μg g?1 fine-grain sediment. The hydrocarbons were dominated by the unresolved complex mixture (UCM), with total polycyclic aromatic hydrocarbons (PAHs) concentrations ranging from 4 μg g?1 to 33 μg g?1 fine-grain sediment. Alkyl-substituted compounds (e.g., C1 to C4 methyl groups) of naphthalene, fluorene, phenanthrere + anthracene, and chrysene series dominated the polycyclic aromatic hydrocarbons (PAHs). Polycyclic aromatic hydrocarbons, saturated hydrocarbons, and the unresolved complex mixture (UCM) distributions reflect mixtures of combustion products (i.e., pyrogenic sources) and direct discharges of petroleum products. Total PCB concentrations ranged from 0.075 μg g?1 to 2.6 μg g?1 fine-grain sediment, with highest concentrations in the Anacostia River. Four to six C1-substituted biphenyls were the most-prevalent PCBs. Variability in the PCB distribution was observed in different sampling areas, reflecting, differing proportion of Arochlor inputs and degradation. The concentration of all contaminants was generally higher in sediments closer to known sewer outfalls, with concentrations of total hydrocarbon, PAHs, and PCBs as high as 6,900 μg g?1, 620 μg g?1, and 20 μg g?1 fine-grain sediment, respectively. Highest PCB concentrations were found in two outfalls that drain into the Tidal Basin. Concentrations of organic contaminants from sewers draining to the Washington Ship Channel and Anacostia River had higher concentrations than sediments of the mid-channel or river. Sources of PCBs appear to be related to specific outfalls, while hydrocarbon inputs, especially PAHs, are diffuse, and may be related to street runoff. Whereas most point-source contaninant inputs have been regulated, the importance of nonpoint source inputs must be assessed for their potential addition of contaminants to aquatic ecosystems. This study indicates that in large urban areas, nonpoint sources deliver substantial amounts of contaminants to ecosystems through storm and combined sewer systems, and control of these inputs must be addressed.  相似文献   

2.
Thirty-three bottom sediments were collected from the Potomac and Anacostia rivers, Tidal Basin, and Washington Ship Channel in June 1991 to define the extent of trace metal contamination and to elucidate source areas of sediment contaminants. In addition, twenty-three sediment samples were collected directly in front of and within major storm and combined sewers that discharge directly to these areas. Trace metals (e.g., Cu, Cr, Cd, Hg, Pb, and Zn) exhibited a wide range in values throughout the study area. Sediment concentrations of Pb ranged from 32.0 μg Pb g?1 to 3,630 μg Pb g?1, Cd from 0.24 μg Cd g?1 to 4.1 μg Cd g?1, and Hg from 0.13 μg Hg g?1 to 9.2 μg Hg g?1, with generally higher concentrations in either outfall or sewer sediments compared to river bottom-sediments. In the Anacostia River, concentration differences among sewer, outfall, and river sediments, along with downriver spatial trends in trace metals suggest that numerous storm and combined swers are major sources of trace metals. Similar results were observed in both the Tidal Basin and Washington Ship Channel. Cadminum and Pb concentrations are higher in specific sewers and outfalls, whereas the distribution of other metals suggests a more diffuse source to the rivers and basins of the area. Cadmium and Pb also exhibited the greatest enrichment throughout the study area, with peak values located in the Anacostia River, near the Washington Navy Yard. Enrichment factors decrease in the order: Cd>Pb>Zn>Hg>Cu>Cr. Between 70% and 96% of sediment-bound Pb and Cd was released from a N2-purged IN HCl leach. On average, ≤40% of total sedimentary Cu was liberated, possibly due to the partial attack of organic components of the sediment. Sediments of the tidal freshwater portion of the Potomac estuary reflect a moderate to highly components area with substantial enrichments of sedimentary Pb, Cd, and Zn. The sediment phase that contains these metals indicates the potential mobility of the sediment-bound metals if they are reworked during either storm events or dredging.  相似文献   

3.
《Applied Geochemistry》2001,16(5):541-558
The Isonzo river mouth has been the source of Hg in the Gulf of Trieste (northern Adriatic sea) since the sixteenth century, making this shallow basin one of the most contaminated marine areas in the length of time and amount of metal accumulated. The occurrence and behaviour of total Hg (range 0.064–30.38 μg g−1; average 5.04 μg g−1; median 3.10 μg g−1, n=80) and related size fractions in sediments of this coastal area were investigated in detail. The relationship between total Hg and the fine silt-clay (< 16 μm) fraction has provided information on the hydrological and mineralogical fractionation process affecting this element, when compared to other heavy metals associated with fluvial inputs. Mercury contents are very high along the littoral zone of the northern (Italian) sector where this metal is present in detrital form (cinnabar) in sandy-silty sediments near the river mouth and the surrounding beaches. Within the sediments belonging to the Gulf area, Hg is bound either to fine particles or adsorbed onto the surface of clay minerals and/or partially complexed by colloids and organic matter. Recent accumulation of Hg in a 70 cm long 210Pb dated core, collected in the central part of the Gulf, was also compared to other heavy metals (Fe, Cr, Cu, Mn, Ni and Zn). A preliminary estimate of Hg enrichment shows that the first 50 cm of sediment in the central sector of the Gulf of Trieste are noticeably contaminated, reaching a maximum of up to 25-fold above the proposed natural regional background of 0.17 μg g−1. The vertical trend is well correlated to historical data of Hg extraction activity at the Idrija mine.  相似文献   

4.
The burial characteristics and toxicity risks associated with n-alkanes and polycyclic aromatic hydrocarbons (PAHs) in the riverine and estuarine sediments of the Daliao River watershed were investigated based on three sediment cores. The sum of the n-alkane and PAH concentrations, normalized to organic carbon (OC), ranged from 0.27 to 63.09 μg g?1OC?1 and 6.60 to 366.20 μg g?1OC?1, respectively. The features and the history of industrial activities, such as the oil and chemical industries and port activities near the river and estuary, resulted in different distributions and sources of hydrocarbons. The sources of pollution were identified based on n-alkane indexes and on diagnostic ratios of PAHs. The diagnostic ratios indicated that the n-alkanes were derived from both biogenic and petrogenic sources in different proportions and that the PAHs were derived primarily from petrogenic combustion sources. A hierarchical cluster analysis grouped the core samples into two clusters. The first cluster, river sediments, corresponded to industrial activities; the second cluster, estuarine sediments, corresponded to port shipping activities. The toxic potency of the PAHs in the cores was assessed in terms of toxic equivalents (TEQs) of dibenzo[a,h]anthracene and benzo[a]pyrene. The top layer of the sediment in the cores had a relatively high toxicity. The TEQ values for benzo(a)pyrene (TEQBaP) and dioxins (TEQTCDD) furnished a consistent assessment of the PAHs in the sediment cores.  相似文献   

5.
《Applied Geochemistry》1995,10(2):175-195
Sediments in Halifax Harbour have accumulated contaminant metals Hg, Cu, Zn, and Pb as a result of discharge of untreated sewage and industrial waste, leaching of land fill waste, and surface drainage. Concentrations of contaminants in210Pb dated sediment cores became significant about 1880 and rose rapidly after 1900, reaching maximum concentrations in the decades between 1950 and 1980. Mean concentrations of Hg increased from 0.2 μg g−1 in pre 1890 sediments to 1.6 μg g−1 in the 20th century. Similar enrichments for Cu changed the concentration from 26 to 88 μg g−1; for Zn from 90 to 250 μg g−1, and for Pb the increase was from 12 to 206 μg g−1 Statistical factor analyses of geochemical data have been used to identify: (1) primary contaminants directly associated with waste discharge, these include total and organic-bound forms of Cu, Zn, and Pb; (2) secondary contamination attributed to leaching and modification of primary contaminants include acid labile forms of Zn, Ni, and Cu; (3) diagenetic modification of buried sediments are identified by total and labile forms of Mn; (4) dispersion of contaminants from land surface drainage are characterized by fine-grained aluminosilicates. Historical trends in the changing dominance of these environmental factors reflect changes in industrial activity, urban growth, and changes in the use of metals in paints, domestic and industrial chemicals, and in the combustion of fuels.  相似文献   

6.
Pore-water dissolved organic carbon (PWDOC) concentrations were examined in vegetated and bare sediments of aHalodule wrightii seagrass bed, and in a mud bottom sediment of a southern Texas estuary. Temporal variability was examined at diel (dawn and noon) and bimonthly time scales. Distribution patterns of PWDOC were compared with physical, chemical, and biological factors thought to exert control on PWDOC. Concentration of PWDOC, bacterial production, and resultant PWDOC turnover times displayed statistically significant spatial and temporal variability. Concentration of PWDOC ranged from 14 mg C 1?1 to 107 mg C 1?1 of pore water, or 9–71 μg C cm?3 wet sediment. PWDOC was more variable and was approximately 5 times higher than DOC concentrations in the water column. Low PWDOC concentrations (mean = 14.6 μg C cm?3) and high bacterial production rates (mean = 1.92 μg C cm?3 h?1) were observed at the mud station, whereas PWDOC concentrations were high (mean = 24.6 μg C cm?3) and bacterial production rates were low (mean = 0.43 μg C cm?3 h?1) at the bare station. PWDOC turnover times (Tt), assuming 50% bacterial growth efficiency (1–840 h) were shortest at the mud station (mean=13 h) and longest at the bare station (mean=180 h). In the overlying water column, Tt values were longer, ranging from 1,000–10,000 h. PWDOC concentrations were 25% higher in vegetated sediments than in neighboring bare sediments. This difference was probably due to inputs of labile photosynthetic excretia, since bacterial production rates in vegetated sediments displayed significant diel variability and were 4 times greater than that of bare sediments. Based upon the entire data set, PWDOC was significantly related to macrofaunal biomass, sediment POC, sediment C:N ratios, and oxygen metabolism, but was significantly correlated only to the latter two variables in stepwise multiple regression. Our findings suggest that organism activities and detrital quality are the major determinants controlling variability in PWDOC.  相似文献   

7.
The Isthmus of Tehuantepec corresponds to the shortest distance (~200?km) between the Gulf of Mexico and the Pacific Ocean in Southern Mexico, and the main economical activity of this region is oil extraction and refining. Polycyclic aromatic hydrocarbons (PAHs) and total petroleum hydrocarbons (TPHs) were determined in a 210Pb dated sediment core collected from the continental shelf of Tehuantepec Gulf, in the vicinity of the oil refinery of Salina Cruz, Oaxaca, the main oil refining facility of the country. The sediments were mostly of coarse nature and hence PAHs and TPHs concentrations throughout the core (61?C404???g?g?1 and 29?C154?mg?kg?1, respectively) were below international quality benchmarks. Depth profiles of both PAHs and TPHs concentrations showed increasing trends since the early 1900s but the higher values were found from the 1950s to present. PAH congener ratios showed that these contaminants had both petrogenic and pyrolitic sources, although the former has been predominant since the 1970s. The Salina Cruz refinery started operations in 1978 but the oil industry activities in the Tehuantepec Isthmus go back to the beginning of the twentieth century with the operation of Minatitlan refinery in the Gulf of Mexico, and the Gulf of Tehuantepec being the main conduit for oil distribution in the Pacific coast. The observed changes in contaminant distributions described well the oil industry development in the area.  相似文献   

8.
Methods were developed for determining rates of denitrification in coastal marine sediments by measuring the production of N2 from undisturbed cores incubated in gas-tight chambers. Denitrification rates at summer temperatures (23°C) in sediment cores from Narragansett Bay, Rhode Island, were about 50μmol N2m?2 hr?1. This nitrogen flux is equal to approximately one-half of the NH+4flux from the sediments at this temperature and is of the magnitude necessary to account for the anomalously low N/P and anomalously high O/N ratios often reported for benthic nutrient fluxes. The loss of fixed nitrogen as N2 during the benthic remineralization of organic matter, coupled with the importance of benthic remineralization processes in shallow coastal waters may help to explain why the availability of fixed nitrogen is a major factor limiting primary production in these areas. Narragansett Bay sediments are also a source of N2O, but the amount of nitrogen involved was only about 0.2 μmol m?2 hr?1 at 23°C.  相似文献   

9.
Analytical data are reported for As, Bi, Sb, Se and Te in fifty five geological reference materials (RM). The method used is based on hydride generation inductively coupled plasma-mass spectrometry (HG-ICP-MS) following digestion of the samples in the mixed acid attack of HF-HClO4-HNO3-HCl. Analytes were separated from potential interferences by coprecipitation with La(OH)3. This scheme results in method detections limits of: 1 ng g?1 for Bi and Te; 6 ng g?1 for Sb and Se; and 10 ng g?1 for As. The average relative standard deviation (RSD) for three 0.5 g subsamples of each RM analysed by this method are: 3.7% for As in the range 0.35-187 μg g?1; 5.6% for Sb in the range 0.03-22 μg g?1; 6.8% for Bi in the range 0.002-48 μg g?1; 7.2% for Se in the range 6-3610 ng g?1; and 9.0% for Te in the range 2-445 ng g?1.  相似文献   

10.
An analytical procedure has been developed to measure in situ the 11 B/10 B ratio in terrestrial basaltic rocks and meteoritic chondrules having B concentration of less than 1 μg g?1 using a small radius ims3f ion microprobe. The central difficulties for these measurements are (i) the removal of the trace amount of B contamination introduced in the sample during polishing, (ii) the precise calibration of instrumental mass fractionation of B isotopes and (iii) the low count rates of 10 B and 11 B. Contamination experiments conducted with isotopically labelled B enriched in 10 B showed that ultrasonic cleaning in bi-distilled water (< 1 ng g?1 B) and pre-sputtering of the analysed area decrease B contamination to the level of 0.01 μg g?1. Analyses of isotope standards spanning a range of 11 B/10 B between 3.93 and 4.20 showed that instrumental mass fractionation was constant within? during one session of analyses. Repeated analyses of a standard glass showed a reproducibility of instrumental mass fractionation between February 1991 and October 1996 of 1.3. Taking into account all sources of error, boron isotope measurements are accurate to within 5 for meteoritic samples having B contents in the range 0.1 to 1 μg g?1. A slightly better accuracy of 1.5 can be achieved for basaltic glasses which can be sputtered with very intense primary beams.  相似文献   

11.
The abundances and isotopic compositions of carbon, nitrogen and sulfur were measured in eleven lunar rocks. Samples were combusted sequentially at three temperatures to resolve terrestrial contamination from indigenous volatiles.Sulfur abundances in Apollo 16 highland rocks range from 73 to 1165 μg/g-whereas sulfur contents in Apollo 15 and 17 basalts range from 719 to 1455 μg/g and correlate with TiO2 content. Lunar rocks as a group have a remarkably uniform sulfur isotopic composition, which may reflect the low oxygen fugacity of the basaltic magmas. Much of the range of reported δ34Scd values (?2 to + 2.5 permil) is caused by systematic analytical discrepancies between laboratories.Lunar rocks very likely contain less than 0.1 μg/g of nitrogen. The measured spallogenic production rate, 4.1 × 10?6 μg 15N/g sample/m.y., agrees remarkably closely with previous estimates. An estimate which includes all available data is 3.7 × 10?6 μg15N/g sample/m.y.Lunar basalts may contain no indigenous lunar carbon in excess of procedural blank levels (~0.7 μg/g). Highlands rocks consistently release about 1 to 5 μg/g of carbon in excess of blank levels, but this carbon might either derive from ancient meteoritic debris or be a mineralogie product of terrestrial weathering. The average measured spallogenic 13C production rate is 4.1 × 10?6 μg13C/g sample/m.y. The 13C spallation exposure ages of rocks 15058 and 15499 are 184 and 135 m.y., respectively.  相似文献   

12.
In an attempt to characterize localized rates of sediment accretion, 10 sediment cores were collected from the lower reach of the Passaic River, a major tributary of Newark Bay, New Jersey. Sediments were assayed for 210Pb activity at predetermined depths and the rate of sediment accretion (cm yr?1) was estimated from the least squares regression of the log of unsupported activity versus depth. Sediment accretion rates, derived from 210Pb measurements (RPb) were used to predict the depth interval within the core containing sediments deposited around 1954; subsequent 137Cs analyses were focused on this depth interval. Sediment accretion rates derived from 137Cs measurements (RCs) were extrapolated from the depth of the 1954 horizon. Lead-210 derived sediment accretion rates in cores collected from a sediment bench extending along the inside bend on the southern shore of a meander in the river, ranged from 4.1 cm yr?1 to 10.2 cm yr?1 and averaged 6.8 cm yr?1. The RCs estimates for cores from this area ranged from 3.8 cm yr?1 to 8.9 cm yr?1 and averaged 6.6 cm yr?1. The RCs for cores collected in a more hydrologically dynamic reach of the river upstream of the sediment bench, were only 0.41 cm yr?1 and 0.66 cm yr?1. The results of this investigation indicate that this reach of the lower Passaic River is an area of high sediment accumulation, retaining much of the sediment load deposited from upstream and downstream sources. The rates of sediment accretion in the lower Passaic River are among the highest reported anywhere in the Newark Bay estuary.  相似文献   

13.
Sediment core segments from Sylvan Lake, Lake Champlain and Lake Canadarago were dated radiometrically with 210Pb and 137Cs. Their respective sedimentation rates were determined to be 0.11, 0.14 and 0.52 g cm?2 yr?1. For the two lakes of lower sedimentation the variations of selected elemental abundances as function of depth were analyzed. Two groupings were found: Al, K, Ti, Rb and Zr were correlated among themselves but reflected different variations in the input of terrigenous erosion material to the lakes. The Cu, Zn and Pb correlated among themselves showed similar depth dependence with increasing concentrations toward the top which can be attributed to cultural pollution. Recent ‘excess’ fluxes to the sediments above the natural contribution by clastic material were derived for the location of the cores, which for Cu, Zn and Pb amounted to 3.8, 24 and 16 μg cm?2 yr?1 respectively for Sylvan Lake and 4.9, 20 and 16 μg cm?2 yr?1 for Lake Champlain. The corresponding 210Pb flux was 3.3 and 2.3 dpm cm?2 yr?1, respectively for the two lakes.Approximate residence times in the water column were obtained for trace metals at the Lake Champlain location. Short residence times estimated for Pb (< 0.15 yr) and Cu (< 0.4 yr) indicate fast removal, whereas those for Zn (1.0 ± 0.3 yr) and Cr (2.0 ± 0.5 yr) appeared to be dominated by the water residence time.  相似文献   

14.
Sediment cores from two locations in Green Bay and two in lake Michigan were analyzed for 12 polycyclic aromatic hydrocarbons (PAHs), loss-on-ignition (LOI),210Pb,137Cs, and7Be to study differences in deposition patterns between the freshwater estuary Green Bay, with several local sources, and the open Lake Michigan, dominated by atmospheric inputs. We found that the remote sites receive relatively less high-molecular weight PAHs such as ideno(1,2,3-cd)pyrene and dibenz(ah)anthracene and are more depleted in anthracene and pyrene. This may be related to a low Henry’s law constant for the high molecular compounds and to selective photo-oxidation of anthracene and pyrene during transport. While sedimentation rates are higher in Green Bay than in the open lake, the PAH levels are generally comparable (0.3–8.5 μg g?1) in the two areas. However, the highest PAH levels are found in a core from Green Bay (GB88G). The two Green Bay cores have total PAH concentration maxima in 1985, which appear to be related to the combustion of petroleum. Also, one Green Bay core (GB88G) and the two from Lake Michigan exhibit PAH maxima in the early 1950s in agreement with observations from other study areas. There is a significant correlation between total PAH and LOI, and thus total organic carbon, for the Green Bay cores, but little or no such correlation for the Lake Michigan cores. This may indicate that PAHs in Green Bay are effectively scavenged by settling detritus.  相似文献   

15.
Two sites in the eastern Fram Strait, the Vestnesa Ridge and the Yermak Plateau, have been surveyed and sampled providing a depositional record over the last glacial‐interglacial cycle. The Fram Strait is the only deep‐water connection from the Arctic Ocean to the North Atlantic and contains a marine sediment record of both high latitude thermohaline flow and ice sheet interaction. On the Vestnesa Ridge, the western Svalbard margin, a sediment drift was identified in 1226 m of water. Gravity and multicores from the crest of the drift recovered turbidites and contourites. 14C dating indicates an age range of 8287 to 26 900 years BP (Early Holocene to Late Weichselian). The Yermak Plateau is characterized by slope sediments in 961 m of water. Gravity and multicores recovered contourites and hemipelagites. 14C ages were between 8615 and 46 437 years BP (Early Holocene to mid‐Weichselian). Downcore dinoflagellate cyst analyses from both sites provide a record of changing surface water conditions since the mid‐Weichselian, suggesting variable sea ice extent, productivity and polynyas present even during the Last Glacial Maximum. Four layers of ice‐rafted debris were also identified and correlated within the cores. These events occurred ca at 9, 24 to 25, 26 to 27 and 43 ka, asynchronous with Heinrich layers in the wider north‐east Atlantic and here interpreted as reflecting instability in the Svalbard/Barents Ice sheet and the northward advection of warm Atlantic water during the Late Weichselian. The activity of the ancestral West Spitsbergen Current is interpreted using mean sortable silt records from the cores. On the Vestnesa Ridge drift the modern mass accumulation rate, calculated using excess 210Pb, is 0·076 g cm?2 year?1. On the Yermak Plateau slope the modern mass accumulation rate is 0·053 g cm?2 year?1.  相似文献   

16.
Niobium and Ta concentrations in MPI‐DING and USGS (BCR‐2G, BHVO‐2G, BIR‐1G) silicate rock glasses and the NIST SRM 610–614 synthetic soda‐lime glasses were determined by 193 nm ArF excimer laser ablation and quadrupole ICP‐MS. Measured Nb and Ta values of MPI‐DING glasses were found to be consistently lower than the recommended values by about 15% and 25%, respectively, if calibration was undertaken using commonly accepted values of NIST SRM 610 given by Pearce et al. Analytical precision, as given by the 1 s relative standard deviation (% RSD) was less than 10% for Nb and Ta at concentrations higher than 0.1 μg g?1. A significant negative correlation was found between logarithmic concentration and logarithmic RSD, with correlation coefficients of ‐0.94 for Nb and ‐0.96 for Ta. This trend indicates that the analytical precision follows counting statistics and thus most of the measurement uncertainty was analytical in origin and not due to chemical heterogeneities. Large differences between measured and expected Nb and Ta in glasses GOR128‐G and GOR132‐G are likely to have been caused by the high RSDs associated with their very low concentrations. However, this cannot explain the large differences between measured and expected Nb and Ta in other MPI‐DING glasses, since the differences are normally higher than RSD by a factor of 3. Count rates for Nb and Ta, normalised to Ca sensitivity, for the MPI‐DING, USGS and NIST SRM 612–614 glasses were used to construct calibration curves for determining NIST SRM 610 concentrations at crater diameters ranging from 16 (im to 60 μm. The excellent correlation between the Nb/Ca1μgg‐1 signal (Nb represents the Nb signal intensity; Ca1μg g‐1 represents the Ca sensitivity) and Nb concentration, and between the Ta/Ca1μg g‐1 signal (where Ta represents the Ta signal intensity; Ca1μg g‐1 represents the Ca sensitivity) and Ta concentration (R2= 0.9992–1.00) in the various glass matrices suggests that matrix‐dependent fractionation for Nb, Ta and Ca was insignificant under the given instrumental conditions. The results confirm that calibration reference values of Nb and Ta in NIST SRM 610 given by Pearce et al. are about 16% and 28% lower, respectively. We thus propose a revision of the preferred value for Nb from 419.4 ± 57.6 μg g?1 to 485 ± 5 μg g?1 (1 s) and for Ta from 376.6 ± 77.6 μg g?1 to 482 ± 4 μg g?1 (Is) in NIST SRM 610. Using these revised values for external calibration, most of the determined average values of MPI‐DING, USGS and NIST SRM 612–614 reference glasses agree within 3% with the calculated means of reported reference values. Bulk analysis of NIST SRM 610 by standard additions using membrane desolvation ICP‐MS gave Nb = 479 ± 6 μg g?1 (1 s) and Ta = 468 ± 7 μg g?1 (1 s), which agree with the above revised values within 3%.  相似文献   

17.
Three cores, one kilometer apart, from each of seven locations along Lake Erie were analyzed for heavy metals and dated by 210Pb techniques. The sedimentary record of anthropogenic inputs of heavy metals parallels the increasing intensity of cultural activity in the lake basin. On the average, pollution sources annually contribute 0.4 μg of Cd, 12 μg of Cu, 12 μg of Pb and 36 μg of Zn deposited per each cm2 of the Eastern Basin sediments: 0.5, 8.8, 11 and 31 μg of Cd, Cu, Pb and Zn, respectively, deposited per cm2 of Western Basin sediments and 0.7, 1.4, 2.0 and 5.6 μg of Cd, Cu, Pb and Zn, respectively, deposited per cm2 of fine-grained sediments in the Central Basin. These anthropogenic flux rates exceed the pre-colonial data by 80–600%. The mean flux rates for 210Pb into the Eastern. Central and Western Basins are 0.45, 0.07 and 0.15dpm cm?2 yr?1. respectively. From an inventory of sources and sinks of the metals, it is shown that about 2500 × 103 kg of Cu. 1900 × 103 kg of Pb and 6750 × 103kg of Zn are delivered annually into the lake. The calculated retention in the lake sediments of 45%, 65% and 35% of the total annual inputs of Cu. Pb and Zn, respectively, agrees closely with the accumulation of data derived from sediment analyses. Sewage discharges, direct and indirect, are shown to be an important source of metal in the lake. The mean residence times in the water column are inferred to be 104 days for Cu. 180 days for Pb and 152 days for Zn.  相似文献   

18.
Trends in the spatial distribution of chlorophylla (chla) and colloidal and total carbohydrates on the Molenplaat tidal flat in the Westerschelde estuary, Netherlands, reflected spatial differences in physical properties of the sediment. Results from a Spearman Rank Order Correlation indicated that many of the physical and biological measures covaried. Multiple regression analyses describing the relationship between colloidal carbohydrates and sediment properties resulted in several highly significant equations, although in all cases chla was able to predict colloidal carbohydrate content. Relationships between sediment surface chla and colloidal carbohydrate, and sediment erodibility (i.e., critical erosion threshold, Ucrit, and mass of sediment eroded at a velocity of 30 cm s?1) determined in annular flume experiments were examined. Overall sediment erodibility was lowest (i.e., high thresholds, low mass eroded) for the siltiest sediments in June 1996 when chla and colloidal carbohydrates were high (56.9 μg gDW?1 and 320.6 μg gluc.equ. gDW?1, respectively), and greatest (i.e., low thresholds, high mass eroded) at the sandier sediments in September 1996, when chla and colloidal carbohydrates were low (1.0 μg gDW?1 and 5.7 μg gluc.equ. gDW?1, respectively). When sediments were grouped according to relative silt content, the most significant relationships were found in muddy sand with a finegrained fraction (<63 μm) of 25–50%. Thresholds of erosion increased, while mass of sediment eroded decreased, with increasing chla and colloidal carbohydrate. A similar trend was observed for the sand-muddy sand (63 μm 10–25%). In the sand (63 μm 0–10%), there were no relationships for Ucrit, whereas mass eroded appeared to increase with increasing chla and colloidal carbohydrate. The increased carbohydrate may stick sand grains together, altering the nature of erosion from rolling grains to clumps of resuspension.  相似文献   

19.
Dissolved and particulate hydrocarbons of biogenic origin were investigated for the first time in surface waters along the Seine River and its estuary. They comprise n-alkanes (n-ALKs) and diagenetic polycyclic aromatic hydrocarbons (PAHs). Samples were collected in three different sections of the estuary: the riverine zone, the mixing zone, and the marine zone. At the river mouth, two mooring stations were used for the collection of samples over tidal cycles. Total particulate n-ALK concentrations ranged from 31 ng 1?1 to 2,918 ng 1?1, or 5 μg g?1 dry ng 1?1, or 2 μg g?1 of SM. Concentrations varied with the SM load and could be related to sedimentation and estuarine mixing. The sources of the n-ALKs were different in each zone of the estuary. The dissolved n-ALKs displayed lower concentrations than the particulate phase, varying from 136 ng 1?1 to 344 ng 1?1, while biogenic dissolved PAHs were almost absent.  相似文献   

20.
Sediment accumulation rates were estimated from-the vertical distribution of excess Pb-210 measured in sediment cores collected at seven stations in the Saguenay Fjord, Quebec. These rates decrease with increasing water depth and distance from the mouth of the Saguenay River, ranging from 4.0 g cm?2 yr?1 (～- 7 cm yr?1) near the head of the fjord to 0.07 g cm?2 yr?1 (～- 0.1 cm yr?1) in the deep inner basin of the fjord. In one core from the head of the fjord, layered sediment structures, having different physical characteristics and composition, appear related to recent, pulsed inputs of older raised marine deposits displaced by a landslide in 1971. Synchronous depositional anomalies in several cores provide evidence of other large scale sediment redistribution processes in the fjord. Pb-210 geochronologies are generally in good agreement with time-stratigraphic horizons inferred both from Cs-137 activity profiles and from the analysis of pollen assemblages in one core.  相似文献   

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