Natural radionuclides in the Arabian Sea and Bay of Bengal: Distribution and evaluation of particle scavenging processes

Vertical and temporal variations in the activities of²³⁴Th,²¹⁰Po and²¹⁰Pb have been measured, in both dissolved and paniculate phases, at several stations in the eastern Arabian Sea and north-central Bay of Bengal. A comparative study allows us to make inferences about the particle associated scavenging processes in these two seas having distinct biogeochemical properties. A common feature of the²³⁴Th profiles, in the Arabian Sea and Bay of Bengal, is that the dissolved as well as total (dissolved + particulate) activity of²³⁴Th is deficient in the surface 200 m with respect to its parent,²³⁸U. This gross deficiency is attributed to the preferential removal of²³⁴Th by adsorption onto settling particles which account for its net loss from the surface waters. The scavenging rates of dissolved²³⁴Th are comparable in these two basins. The temporal variations in the²³⁴Th-²³⁸U disequilibrium are significantly pronounced both in the Arabian Sea and Bay of Bengal indicating that the scavenging rates are more influenced by the increased abundance of particles rather than their chemical make-up. In the mixed layer (0–50 m), the scavenging residence time of²³⁴Th ranges from 30 to 100 days. The surface and deep waters of both the seas show an enhanced deficiency of dissolved²¹⁰Po relative to²¹⁰Pb and that of²¹⁰Pb relative to²²⁶Ra. The deficiencies of both²¹⁰Po and²¹⁰Pb in the dissolved phases are not balanced by their abundance in the particulate form indicating a net loss of both these nuclides from the water column. The scavenging rates of²¹⁰Po and²¹⁰Pb are significantly enhanced in the Bay of Bengal compared to those in the Arabian Sea. The mean dissolved²¹⁰Po/²¹⁰Pb and²¹⁰Pb/²²⁶Ra activity ratios in deep waters of the Bay of Bengal are ∼ 0.7 and 0.1, respectively, representing some of the most pronounced disequilibria observed to date in the deep sea. The Bay of Bengal and the Arabian Sea appear to be the regions of most intense particle moderated scavenging processes in the world oceans. This is evidenced by the gross disequilibria exhibited by the three isotope pairs used in this study.     

Sedimentary geochemical record of historical anthropogenic activities affecting Guanabara Bay (Brazil) environmental quality

A sediment core from Guanabara Bay (Brazil) was analyzed for ²¹⁰Pb dating, grain size, total organic carbon (TOC) and total nitrogen, carbon stable isotope ratio (δ¹³C), nitrogen stable isotope ratio (δ¹⁵N) and the metals Fe, Mn, Ni, Co, Cu, Pb, V and Zn, to assess the influence of land use changes on the aquatic system in a region for which large industrial and urban development is expected in the next few decades. To obtain baseline data for improving the monitoring of the expected increase in anthropogenic impacts from surrounding drainage basins, a multivariate analysis of data from different sediment layers was carried out to evaluate the dated sediment record. The geochemical data suggested three different sedimentary phases along the last 200 years. Before the 1880s, the highest clay and TOC contents were observed, where the C/N ratios and the δ¹³C values suggested a mixture of algal and terrestrial organic matter and the lowest concentrations of Co, Cu, Pb, V and Zn, for which background levels were estimated (4.6, 2.7, 14.9, 24.3 and 70.2 mg kg⁻¹, respectively). From the 1880s to the 1950s, the metal concentrations and sand particles increased, but no change in organic matter quality was observed, reflecting a period of land use change, still without significant sewage input. After the 1950s, the sedimentation rate increased from 0.42 to 0.77 cm year⁻¹ and increasing urban sewage input was evidenced by lower C/N ratios, higher δ¹⁵N, decrease of Fe and Mn concentrations and increased fluxes of metals and TOC, which showed a good relationship with population growth data.     

Trace metal and radionuclide pollution in marine sediments of the Aegean Sea (Izmir Bay and Didim)

To determine radioactivity and trace metal levels, surface sediments were collected from two important areas (?zmir Bay and Didim) in the Aegean Sea region of Turkey, and were analyzed for concentrations of ²¹⁰Po, ²¹⁰Pb and trace metals (Cd, Cr, Cu, Fe, Mn, Ni, Pb and Zn). The average ²¹⁰Po and ²¹⁰Pb massic activities in sediments varied in the range of 24 ± 5 to 126 ± 6 Bq kg^?1 dry wt. and 18 ± 3 to 59 ± 4 Bq kg^?1 dry wt., respectively. Izmir Bay exhibited the highest polonium activities in sediments, likely due to specific sedimentation processes and other sediment characteristics. The trace metal results showed that the Izmir Bay is facing trace metal pollution. The metal concentrations in sediment samples are low compared to those from the other neighboring marine environments.     

Variations of Pb in a mine-impacted tropical river,Taxco, Mexico: Use of geochemical,isotopic and statistical tools

The potential environmental threat from Pb in Mexican rivers impacted by historic mining activities was studied using geochemical, isotopic and statistical methods. Lead geochemical fractionation and factor analysis of fractionated and total Pb indicate that anthropogenic sources have contributed significantly to Pb concentrations, while natural sources have contributed only small amounts. The analyses also indicate that two main processes are controlling the total Pb variation throughout the year in both rivers: erosion with discharge processes, and proportional dilution related to differences in grain-size distribution processes. Bio-available Pb in riverbed sediments was greater than 50% in 80% of the sampling stations indicating a high potential environmental risk, according to the risk assessment criteria (RAC). Nevertheless, based on the environmental chemistry of Pb and on multivariate statistical analysis, these criteria did not apply in this particular case. Significant differences (p < 0.05) in total Pb concentrations (from 50 to 5820 mg kg⁻¹) and in the geochemical fractionation were observed as a function of seasonality and location along the river flow path. In the Cacalotenango and Taxco rivers, the highest concentrations of total Pb were found at stations close to tailings during the rainy and post-rainy seasons. The geochemistry of Pb was mainly controlled, during the dry and post-rainy seasons by the organic matter and carbonate content, and in the rainy season by hydrological conditions (e.g., the increase in river flux), hydrological basin erosion, and the suspended solids concentration. Isotopic analyses of the ²¹⁰Pb/²¹⁴Pb ratio showed three processes in the Cacalotenango and Taxco rivers. First, the accumulation of atmospheric excess ²¹⁰Pb, favoured during calmer hydrodynamic conditions in the river basin commonly during dry periods, is recorded by a ²¹⁰Pb/²¹⁴Pb ratio of >1. In the case of the Cacalotenango river, ²¹⁰Pb did show preferential accumulation in sediments. Second, a ²¹⁰Pb/²¹⁴Pb ratio of <1 in some samples might be indicating (a) the presence of eroded material from weathered tailings with similar ²¹⁰Pb depletion (probably by secular disequilibrium caused by weathering or mining processes, which was observed in both rivers), or (b) preferential transport of Pb and sediments during high energy events (e.g., flow increase, as is the case of Taxco river). Third, no significant changes in the ²¹⁰Pb/²¹⁴Pb ratio might be reflecting a situation where mining material is not entering the system, or where hydrodynamic changes throughout the year of equal magnitude allow the system to reach a new equilibrium for the ²¹⁰Pb/²¹⁴Pb ratio. Finally, based on these results it is recommended that inhabitants of the studied area avoid using water from the Cacalotenango river in the rainy and post-rainy seasons, and to take precautions for its use in the dry season, such as allowing suspended material to settle before use, and that they should avoid use of Taxco river water at all times.     

Transport and sediment accumulation of210Pb and137Cs in two Southeast Alaskan fjords

Sediment profiles of²¹⁰Pb and¹³⁷Cs in cores collected at increasing distances from the heads of Smeaton Bay and Boca de Quadra fjords indicate that watersheds influence the inventories of radioisotopes present and that the steep topographies of the fjords enhance sediment redistribution. Episodic deposition of terrestrially derived sediment was responsible for roughly 50% of the¹³⁷Cs and 45% of the²¹⁰Pb inventories in shallower (less than 180 m) locations in Wilson and Bakewell arms of Smeaton Bay.²¹⁰Pb sedimentation rates at shallower sites when corrected for episodic deposition were less than sedimentation rates obtained in the deep basins of the fjords where sediment focusing and increased primary productivity in the overlying water column occur. Higher fluxes of dissolved Mn from surficial sediments and subsequent reoxidation in the overlying water may have enhanced scavenging of²¹⁰Pb in basin locations, resulting in higher inventories. Episodic events have occurred frequently in Smeaton Bay and Boca de Quadra suggesting that steady-state conditions with respect to sedimenting particles can be achieved only when averaged over long time periods approaching the time over which¹³⁷Cs and²¹⁰Pb are useful.     

Geochemical and Sr–Nd–Pb-Isotope Characteristics of Ice-Rafted Sediments of the Arctic Ocean

The paper discusses the geochemical and Sr–Nd–Pb-isotope data on ice-rafted sediments (IRS) from different areas of the Arctic Ocean. Samples were collected during the Cruise of R/V Polarstern between Spitsbergen and North Pole, Yermak Plateau, as well as in Fram Strait. It is shown that the studied IRS samples in terms of La_N/Yb_N and εNd values are close to the composition of suspended particulate matter (SPM) from the mouth parts of large rivers and rivers transporting the sedimentary erosion products. This also follows from their Th/Sc, Th/Co, La/Sc, La/Sm, Sc/Th ratios and Sc content and from the position of their data points in the Sc–Th/Sc, La/Sc–Th/Co, and La/Sm–Sc/Th diagrams between the average SPM compositions of the Ob and Lena rivers. The values of ²⁰⁷Pb/²⁰⁶Pb and εNd in IRS samples give grounds to suggest that the rock complexes of the European, North American, and Asian continental margins could be potential sources for this sedimentary material. In the ²⁰⁷Pb/²⁰⁶Pb–εNd diagram, the IRS samples from all three studied areas define a compact cluster and are mainly confined to the triangle with corners represented by the Mackenzie River, Okhotsk–Chukotka volcanic area, and Lena River, being closer to the latter. In the Sm/Nd–εNd diagram, IRS points also form a compact field, being located almost in the middle between the average SPM compositions of the Yenisei and Ob rivers, on the one hand, and Lena River, on the other. In all diagrams, IRS samples from the different West Arctic areas show no significant scatter. With allowance for the fact that sediments are not subjected to significant homogenization during ice rafting, sediments from all three areas were obtained from a common source. As seen from the position of IRS data points in the ⁸⁷Sr/⁸⁶Sr–εNd diagram, this source was the Asian continental margin.     

Hydrographic surveys and sedimentation in Deep Bay,Hong Kong

Three hydrographic surveys were carried out in Deep Bay, which is located in the eastern part of Pearl estuary between Shenzhen, the most successful special economic zone of PRC, and Hong Kong. Data on current, size distributions of bottom sediment, suspended solids, and some water quality parameters were obtained. This information is of value for mathematical modeling of tidal circulation and sediment transport in the bay, and also useful in the planning of further development in this area. The sedimentation rate in Deep Bay was estimated by two different approaches, viz. comparison of historical navigation maps and²¹⁰Pb dating. Information obtained from the maps indicated that average sedimentation rate between 1898 and 1949 was about 8 mm/yr, while a 15 mm/yr figure was obtained from the²¹⁰Pb dating for recent years.     

Lead isotopic systematics of major river sediments: a new estimate of the Pb isotopic composition of the Upper Continental Crust

The lead isotopic composition of river sediments is reported in the present work for the Earth's major river basins, from old cratonic to young orogenic areas and from subarctic to tropical climates. Sediment samples from these large river basins provide a useful tool to calculate the average upper crustal composition because they are large-scale integrated samples of the weathering products of the present-day Upper Continental Crust (UCC). Two different and complementary calculations were done to estimate the average lead isotopic composition of the UCC. The first, based on the flux weighted average of particulate lead delivered by the rivers, gave values of 19.07, 15.74 and 39.35 for ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb ratios, respectively. To avoid over-estimating the contribution of orogenic areas, which produces a bias (because the flux of particulate lead depends strongly on the physical erosion rate), a second calculation was done by averaging with drainage areas of each river basin. This gave values of 18.93, 15.71 and 39.03 for ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb ratios, respectively. These direct calculations of the lead isotopic composition of the UCC are similar and are in agreement with previous estimates made using an indirect approach.     

Genetic variation in the oyster,Crassostrea virginica (Gmelin), in relation to environmental variation

Four polymorphic loci in seven natural oyster (Crassostrea virginica Gmelin) populations of the Chesapeake Bay were analyzed by protein-gel electrophoresis for genetic variation. Samples of about 100 each were taken in 1977 along environmental gradients from stations in the James and Potomac rivers. The distribution of genotypes at four loci for each of the stations was nog significantly different from Hardy-Weinberg expectations. At two loci (Pgi andLap-2), a pool of all seven stations was also in equilibrium. Significant genetic differentiation between rivers was detected for two other loci (Pgm-1 andLap-1), and frequency of one genotype (Lap-1 ^95/95) was significantly correlated with mean temperature over the water monitoring period (1972–1977).     

Polycyclic aromatic hydrocarbons in dated sediments from Green Bay and Lake Michigan

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.     

Regional variations in atmospheric deposition and sources of anthropogenic lead in lake sediments across the Canadian Arctic

Stable Pb isotope profiles in dated lake sediment cores were used to gauge the relative amounts and possible sources of anthropogenic Pb deposited from the atmosphere in different regions of the Canadian Arctic. A distinct north-south difference was found. In four High Arctic lakes (i.e., north of 66°N) in this study, recent Pb isotopic shifts or concentration increases attributable to anthropogenic Pb were negligible. The maximum possible contribution from anthropogenic Pb was 0 to 19% of acid-leachable Pb in the 1980s or 1990s. In contrast, two lakes in the Hudson Bay region displayed significantly lower Pb isotope ratios and threefold to fivefold increases of Pb concentrations in modern sediments, corresponding to anthropogenic Pb inputs of at least 72 to 91% of leachable Pb. Eurasian urban and industrial Pb is known to dominate the High Arctic atmosphere. A possible explanation for its negligible influence on northern lake sediments is that atmospheric Pb deposition at northern latitudes is reduced compared with southern regions and is small compared to local geological inputs. ²¹⁰Pb deposition declines with increasing latitude, apparently because of declining precipitation rates; stable Pb deposition may be similarly affected. Meteorological considerations and variations in the post-1900 Pb isotopic trajectories indicated that the predominant anthropogenic Pb source region in NW Hudson Bay was Eurasia, while in SE Hudson Bay, it was Canada and the United States, with a minor Eurasian component.     

Dynamics of sediment and contaminant transport in the Hudson River estuary: Evidence from sediment distributions of naturally occurring radionuclides

Near surface (<10 cm) sediment distributions of²³⁴Th sampled multiple times at five locations along the axis of the Hudson Estuary from the Upper Bay of New York to Haverstraw Bay are compared with²¹⁰Pb data from longer cores at the same locations. The comparison indicates that while there is little net sediment accumulation anywhere except at one location in the Upper Bay, near surface sediment in this reach of the estuary is mobile on short (months) time scales. The sediment appears to be physically mixed rather than bioturbated. Comparison of the sediment inventories of²³⁴Th with calculated water column production indicates short time scale (months) variability in²³⁴Th deposition. Some parts of the bottom have²³⁴Th inventories in excess of local production but these appear to be balanced by²³⁴Th deficient areas, resulting in a general equilibrium. Sediment inventories of Pb, Cu, and Zn normalized to²¹⁰Pb show no evidence of a uniquely urban source of these metals to the lower estuary. Silver distributions in sediment indicate a possible source of silver from New York City, probably related to sewage inputs.     

Tholeiitic Aleutian arc plutonism: The Finger Bay pluton,Adak, Alaska

The earliest representatives in the sequence of Tertiary to Recent magmatic rocks on Adak island in the central Aleutians, are the Finger Bay Volcanics and associated small shallow-level gabbroic intrusives. The tholeiitic Finger Bay pluton (gabbro to quartz monzodiorite) is among the least altered representatives of this earliest period. The field relations, mineralogy, and geochemistry of the Finger Bay pluton contrast with the more recent calcalkaline plutons in the arc (e.g. on Adak, Hidden Bay pluton: 33 m.y. and on Kagalaska, Kagalaska pluton: 15 m.y.). Compared with the Hidden Bay pluton, the Finger Bay pluton is smaller (8 km² versus 100 km²), has a greater proportion of gabbro (84% versus 5%), has a somewhat different mineralogy, and has higher whole rock and mafic mineral FeO/MgO ratios, higher K₂O, and higher concentrations of incompatable elements in rocks of equivalent SiO₂ (particularly for the more siliceous units). Magmatic amphibole occurs only in the most siliceous units in the Finger Bay pluton, whereas it is common in the calc-alkaline plutons. Except for the size, these differences parallel those between tholeiitic and calc-alkaline volcanic rocks from the active Aleutian volcanic centers. Textural, miner-alogical, and trace element analyses indicate that mixing of magmas and gabbros generated some of the rocks of intermediate (monzodiorite) composition in the Finger Bay pluton. Most of the differences in magmatic trends between the calc-alkaline and tholeiitic plutons are attributed to the physical conditions of magmatic evolution in the crust, rather than to differences in initial magmatic types. This conclusion rests on the similarity of fractionation-independent isotope ratios and trace element ratios in Aleutian magmas of all ages. In particular, compared to magmas of the north Pacific ocean basin (MORB, oceanic islands), Aleutian magmas show excess enrichment of Ba, K, Rb, and U relative to REE and high ²⁰⁷Pb/²⁰⁴Pb ratios for a given ²⁰⁶Pb/²⁰⁴Pb ratio. Recognition of tholeiitic series plutons in the arc provides direct evidence for magmatic conditions accompanying fractionation, and serves to emphasize the diversity of magmatic trends that are found over time and space at convergent plate margins.     

Lead isotope distribution and enrichment factors in soil profiles around an abandoned Pb-smelter plant

Todos os Santos (all Saints) Bay area on Brazil’s east coast is known for one of the most significant cases of lead contamination in the country owing to the past activities of a Pb-smelter plant. This work was carried out to assess the concentration and sources of Pb based on Pb isotopes and enrichment factor of soil profiles surrounding Todos os Santos Bay in order to understand the expansion of contamination and to help the establishment of Pb regulatory standards for the region. Forty-four samples were collected from soil genetic horizons of six pedons that represent the range of dominant soil properties and geologic materials in the region. Concentrations of Pb and the isotopes ²⁰⁴Pb, ²⁰⁶Pb, ²⁰⁷Pb, and ²⁰⁸Pb were determined on an inductively coupled plasma (quadrupole) mass spectrometry. The soil enrichment factor was calculated using Al and Fe as conservative index elements. Average Pb concentration (15.87 mg kg^?1) in uppermost horizons (from all six pedons) is slightly higher than soil background concentrations commonly reported in Brazil. Samples feature a wide range of Pb isotope ratios, ranging from 36.71 to 47.38 for ²⁰⁸Pb/²⁰⁴Pb, 15.00 to 15.65 for ²⁰⁷Pb/²⁰⁴Pb, 16.86 to 20.59 for ²⁰⁶Pb/²⁰⁴Pb, and 1.10 to 1.31 for ²⁰⁶Pb/²⁰⁷Pb. For the enrichment factor calculations, only Fe demonstrated a good agreement with Pb isotopic ratios. Both Pb isotopic composition and enrichment factor were useful tools to distinguishing natural and anthropogenic influence on the Pb soil concentrations.     

Temporal Trends of Dissolved Trace Metals in Jamaica Bay,NY: Importance of Wastewater Input and Submarine Groundwater Discharge in an Urban Estuary

Jamaica Bay, NY, is a highly urbanized estuary within the boroughs of New York City conspicuously lacking published information on dissolved trace metal concentrations. The current study examines the distribution and cycling of trace metals in that embayment with data gathered during cruises in November 2004, April 2005, and June 2006. Most of the metal distributions (Fe, Zn, Co, Ag, Cu, Pb, Ni) in the water column are explained by the input of substantial volumes of treated wastewater effluent. However, several lines of evidence suggest that submarine groundwater discharge (SGD) is also an important source of dissolved Fe, Zn, Co, Ni, and isotopically distinct stable Pb ratios (²⁰⁶Pb, ²⁰⁷Pb, ²⁰⁸Pb) in the Bay. Conversely, the recirculated seawater component of SGD is an apparent sink for dissolved Mo. This study provides the first measurements of dissolved trace metals in the Jamaica Bay water column and subterranean estuary and provides evidence for trace metal input due to SGD.     

Pb isotopic variability in the modern-Pleistocene Indus River system measured by ion microprobe in detrital K-feldspar grains

The western Himalaya, Karakoram and Tibet are known to be heterogeneous with regard to Pb isotope compositions in K-feldspars, which allows this system to be used as a sediment provenance tool. We used secondary ion mass spectrometry to measure the isotopic character of silt and sand-sized grains from the modern Sutlej and Chenab Rivers, together with Thar Desert sands, in order to constrain their origin. The rivers show a clear Himalayan provenance, contrasting with grains from the Indus Suture Zone, but with overlap to known Karakoram compositions. The desert dunes commonly show ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁶Pb/²⁰⁴Pb values that are much higher than those seen in the rivers, most consistent with erosion from Nanga Parbat. This implies at least some origin from the trunk Indus, probably reworked by summer monsoon winds from the SW, a hypothesis supported by bulk Nd and U-Pb zircon dating. Further data collected from Holocene and Pleistocene sands shows that filled and abandoned channels on the western edge of the Thar Desert were sourced from Himalayan rivers before and at 6-8 ka, but that after that time the proportion of high isotopic ratio grains rose, indicating increased contribution from the Thar Desert dunes prior to ∼4.5 ka when flow ceased entirely. This may be linked to climatic drying, northward expansion of the Thar Desert, or changes in drainage style including regional capture, channel abandonment, or active local Thar tributaries. Our data further show a Himalayan river channel east of the present Indus, close to the delta, in the Nara River valley during the middle Holocene. While this cannot be distinguished from the Indus it is not heavily contaminated by reworking from the desert. The Pb system shows some use as a provenance tool, but is not effective at demonstrating whether these Nara sediments represent a Ghaggar-Hakra stream independent from the Indus. Our study highlights an important role for eolian reworking of floodplain sediments in arid rivers such as the Indus.     

Aliphatic petroleum and biogenic hydrocarbons entering Narragansett Bay from tributaries under dry weather conditions

The temporal variability of hydrocarbon inputs from rivers discharging into Narragansett Bay under dry weather conditions, as well as the elucidation of the types and sources of hydrocarbons found in urban rivers, has been investigated. The rivers studied, the Blackstone, the Pawtuxet, the Moshassuck, and the Woonasquatucket, constitute the majority of river flow to the estuary. The unfiltered river water samples were extracted and analyzed for total aliphatic hydrocarbons, including natural and petroleum-derived species. The results of the year-long study revealed consistent oil pollution in all of the rivers sampled. Crankcase oil was ubiquitous, but the presence as well of fuel oils and, particularly in the Moshassuck River, gasoline (or kerosene), demonstrate that these rivers are subject to considerable oil pollution stress. The average concentration of hydrocarbons was ≈37 μg l^?1 which, according to some toxicologists, indicates that sensitive organisms may be under stress. In addition, most samples showed evidence of small amounts of terrigenous plant wax hydrocarbons. Hydrocarbon concentrations are comparable to those in other urban rivers but are higher than in rivers from rural areas; moreover, they did not vary in any systematic way with season. The mass transport of hydrocarbons in each of the rivers generally mimicked trends in river discharge, thereby emitting the lowest mass to the estuary in the summer and increasing throughout the remainder of the year. Moreover, due primarily to relative discharge differences, the Blackstone and Pawtuxet rivers constitute 90% of the total calculated flux of hydrocarbons from all four rivers. By combining the results from this investigation with those from previous studies, it was possible to obtain an estimate of the total annual inputs of these contaminants to Narragansett Bay. Total annual loads from rivers and wastewater treatment facilities were approximately 240 mt. When sources such as wet weather inputs were included, the total increased to 420 mt yr^?1. This value represents direct current inputs to the system and is considerably lower than previously published estimates. The current direct input estimate, while indicative of an improving situation, differs from previous estimates in that the latter were based upon calculations that approximated the long-term loadings from the watersheds, most of which are likely accumulating above the fall-lines of rivers throughout the watershed. Nevertheless, the current loadings represent a significant chronic flux of hydrocarbons to Narragansett Bay. For example, this estimate indicates that an amount equal to approximately 43% of the oil discharged into Narragansett Bay from the recent World Prodigy oil spill enters the estuary from chronic sources every year.     

The distribution of nitrogen speciation and sources of nitrate in the north of Taihu Lake

Meiliang Bay and Gonghu Bay, in the north of Taihu Lake, are important water sources for the city of Wuxi, and increased eutrophication now threatens the safety of drinking water. The distribution of nitrogen (N) speciation and source of N in the surface waters in the north of Taihu Lake is studied, which was an important first step in controlling N pollution. The result shows that the average concentration of ammonia (NH₄ ⁺) and nitrate (NO₃ ^?) of surface water in Meiliang Bay was 0.32 and 0.35 mg/L, while 0.21 and 0.74 mg/L of Gonghu Bay, in which both bays had serious nitrate pollution. The concentrations of NH₄ ⁺ and NO₃ ^? in the surface water of the two bays had a trend of gradual decrease from north to south. The maximum concentrations of NH₄ ⁺ and NO₃ ^? of two bays were observed near the inflowing rivers, and the maximum concentrations of NH₄ ⁺ in surface water of two bays were 0.49 and 0.61, and 0.77 and 1.38 mg/L of NO₃ ^?. The concentration of NH₄ ⁺ in the interstitial water of the two bays had a trend of gradual decrease from west to east, but NO₃ ^? had the opposite tendency. The maximum concentrations of NH₄ ⁺ in the interstitial water of the two bays were 5.88 and 4.64, and 3.58 and 7.18 mg/L of NO₃ ^?. The exchangeable NH₄ ⁺ content in the sediment of Meiliang Bay had a trend of gradual decrease from north to south, but Gonghu Bay showed the reverse. The exchangeable NO₃ ^? content in the sediment of Meiliang Bay had a trend of gradual decrease from east to west, but a decreasing trend from north to south was observed in Gonghu Bay. The maximum concentrations of exchangeable NH₄ ⁺ were determined, and the values were 96.25 and 74.90 mg/kg, as well as NO₃ ^? with the values of 12.06 and 7.08 mg/kg. Chemical fertilizer and domestic sewage were the major sources of nitrate in surface water of Gonghu Bay, contributing 39.16 and 47.79%, respectively. Domestic sewage was the major source of nitrate in Meiliang Bay, contributing 84.79%. The denitrification process in Gonghu Bay was more apparent than in Meiliang Bay. Mixing and dilution processes had important effects on changing the concentration of nitrate transportation in the two bays.     

Retrospective analysis of the impacts of major hurricanes on sediments in the lower Everglades and Florida Bay

A record of the impacts of major hurricanes on sediment stratigraphy and composition in subtropical ecosystems has been preserved in the lower Everglades and Florida Bay. These impacts were observed in discontinuous layers of sediment that were identified from high-resolution, vertical profiles of excess ²¹⁰Pb and ¹³⁷Cs. Discontinuities were found at different geographic locations and at two to three different depths in the sediment column; however, the layers were each deposited within time periods that corresponded with the passing of category 3–5 hurricanes during 1960, 1948 and 1935. A simple mass balance model for excess ²¹⁰Pb was used to show net changes of ±20–100% in excess ²¹⁰Pb inventory that resulted from sediment disturbances of <1 to >22 cm. Abrupt shifts in sediment composition were often observed in hurricane-impacted layers. Ratios of organic (C/P) were four- to fivefold higher than normal in post-hurricane layers of sediment at open bay sites. These layers are phosphorus poor and seem to reflect preferential decomposition of organic P relative to organic C in association with hurricanes. The net effect is for major hurricanes to redistribute sediment, organic matter and nutrients.This revised version was published online in July 2003.     

Historical record of heavy metal pollution deduced by lead isotope ratios in core sediments from the Osaka Bay,Japan

Three marine sediment cores from Osaka Bay were analyzed for ²¹⁰Pb geochronology, heavy metal concentrations (Zn, Cu, and Pb) and stable lead isotope ratios (²⁰⁶Pb/²⁰⁷Pb) in order to reconstruct high-resolution heavy metal pollution history from 1900–2006. Anthropogenic metal accumulation in sediments peaked in 1970 in agreement with the high economic growth period in Japan. The comparison of temporal patterns of ²⁰⁶Pb/²⁰⁷Pb ratio with other areas of Japan suggested that the heavy metals, imported from several different countries during the periods of economic growth (1955 to 1973), are the main pollution source for the country. For the period 1970–2006, the sediment data reflect the result of stricter environmental regulations applied after the late 1960s. However, heavy metal concentrations in the surface sediments are still elevated to levels several times higher than the levels at the bottoms of the cores. Additionally, the lead isotope ratio does not show significant change after the 1980s. Secondary heavy metal pollution through the mixing of deeper polluted sediment appears to be the likely reason for the deterioration of present time submarine sediment environments. In conclusion, this study has demonstrated that it is difficult to recover over a period of several years the benthic quality of a bay, once it is heavily polluted.