The spatial and temporal distribution of heavy metals in sediments of Victoria Harbour, Hong Kong

Victoria Harbour has received substantial loadings of pollutants from industrial and municipal wastewater discharged since the 1950s. Inputs of contaminants have declined dramatically during the last two decades as a result of better controls at the source and improved wastewater treatment facilities. To assess the spatial and temporal changes of metal contaminants in sediments in Victoria Harbour, core and grab sediments were collected. The central harbour areas were generally contaminated with heavy metals. The spatial distribution of trace metals can probably be attributed to the proximity of major urban and industrial discharge points, and to the effect of tidal flushing in the harbour. In the sediment cores, the highest concentrations of trace metals were observed to have accumulated during the 1950s-1980s, corresponding with the period of rapid urban and industrial development in Hong Kong. From the late 1980s, there has been a major decline in the concentrations of trace metals, due to a reduction in industrial activities and to the enactment of wastewater pollution controls in the territory. The Pb isotopic compositions of the sediments revealed the anthropogenic inputs of Pb to the harbour. The (206)Pb/(207)Pb ratios varied from 1.154 to 1.190, which were lower than those of background geological materials in Hong Kong ((206)Pb/(207)Pb: 1.201-1.279). The data also indicated that the Pb in the harbour sediments most likely originated from mixed sources, including the leaded gasoline used in the past and other anthropogenic sources.     

The spatial and temporal distribution of heavy metals in sediments of Victoria Harbour,Hong Kong

Victoria Harbour has received substantial loadings of pollutants from industrial and municipal wastewater discharged since the 1950s. Inputs of contaminants have declined dramatically during the last two decades as a result of better controls at the source and improved wastewater treatment facilities. To assess the spatial and temporal changes of metal contaminants in sediments in Victoria Harbour, core and grab sediments were collected. The central harbour areas were generally contaminated with heavy metals. The spatial distribution of trace metals can probably be attributed to the proximity of major urban and industrial discharge points, and to the effect of tidal flushing in the harbour. In the sediment cores, the highest concentrations of trace metals were observed to have accumulated during the 1950s–1980s, corresponding with the period of rapid urban and industrial development in Hong Kong. From the late 1980s, there has been a major decline in the concentrations of trace metals, due to a reduction in industrial activities and to the enactment of wastewater pollution controls in the territory. The Pb isotopic compositions of the sediments revealed the anthropogenic inputs of Pb to the harbour. The ²⁰⁶Pb/²⁰⁷Pb ratios varied from 1.154 to 1.190, which were lower than those of background geological materials in Hong Kong (²⁰⁶Pb/²⁰⁷Pb: 1.201–1.279). The data also indicated that the Pb in the harbour sediments most likely originated from mixed sources, including the leaded gasoline used in the past and other anthropogenic sources.     

The application of lead isotope ratios in the Antarctic macroalga Iridaea cordata as a contaminant monitoring tool

Lead (Pb) isotope ratios were measured in the marine macroalga Iridaea cordata collected from four locations in the Windmill Islands, East Antarctica. Based on the masses of thalli collected, samples analysed in this study were likely to be a mixture of one and two year old thalli. For a sample of thalli of various ages (<12 months to 2 years old) from the same site there was no apparent variation in Pb concentration or Pb isotope ratio with thallus mass/age, indicating that contaminant sources had been constant over the lifetime of the thalli sampled. I.cordata samples close to the Thala Valley waste disposal site (Brown Bay Inner) near the Australian Station, Casey, displayed isotopic signatures (²⁰⁸Pb/²⁰⁴Pb 35.99; ²⁰⁶Pb/²⁰⁷Pb 1.066; n = 3; average values shown) trending towards that possessed by major Australian Pb sources (Broken Hill and Mt Isa, ²⁰⁸Pb/²⁰⁴Pb 35.60; ²⁰⁶Pb/²⁰⁷Pb 1.041) suggesting that these samples had been exposed to anthropogenic Pb originating from the Thala Valley waste disposal site. Material collected hundreds of metres from the tip location at Brown Bay Outer had isotopic values (²⁰⁸Pb/²⁰⁴Pb 36.32; ²⁰⁶Pb/²⁰⁷Pb 1.088; n = 10) intermediate between Brown Bay Inner and sites further from the contaminant source at Sparkes Bay and Wilkes (²⁰⁸Pb/²⁰⁴Pb 36.46; ²⁰⁶Pb/²⁰⁷Pb 1.094; n = 4) showing that contaminant transport was predominantly restricted to Brown Bay Inner. This study demonstrates that the isotope ratios of Pb in marine macroalgae can provide valuable information as to the origin and extent of heavy metal flux in a marine environment.     

Lead concentrations and isotopes in aerosols from Xiamen, China

To investigate the magnitude and origin of lead (Pb) pollution in the atmosphere of Xiamen, China, 40 aerosol samples were collected from the coast of Xiamen from January to December 2003. All these samples were measured for Pb isotopic compositions (²⁰⁸Pb/²⁰⁶Pb = 2.10897 ± 0.00297, ²⁰⁷Pb/²⁰⁶Pb = 0.85767 ± 0.00159, n = 40) using a Multi-collector-Inductively Coupled Plasma Mass Spectrometer (MC-ICPMS). Thirty-five out of forty samples were also measured for Pb concentrations (79.1 ± 38.3 ng/m³, n = 35) by Atomic Absorption Spectroscopy (AAS). The results indicate that the Pb concentrations display significant seasonal variations while Pb isotopic ratios remain relatively constant. The Pb concentrations were high in January and February, abruptly decreased in March, remained relatively constant (but low) from April to August, and then gradually increased from September to December. This corresponds to the rainless climate in winter and rain scavenging in summer. The higher Pb concentration of Xiamen aerosols in winter and spring may be also caused by long-range transferred anthropogenic Pb during the northeastern monsoon seasons. Although the use of leaded gasoline in Xiamen was banned in 2000, our new data indicate that the Pb annual concentrations of aerosols in Xiamen increased about 12% when compared to the data measured between 1991 and 1993. Thus, Pb pollution in the atmosphere of Xiamen has not receded even after the phase-out of leaded gasoline. Our results further confirm the previous studies’ conclusion that the primary source of atmospheric Pb in China, especially in South China, is the vast combustion of lead-containing coal, not leaded gasoline.     

Anthropogenic lead concentrations and sources in Baltic Sea sediments based on lead isotopic composition

The Gulf of Gdańsk is influenced by heavy metals of anthropogenic origin. In this study, temporal concentration changes of Pb, Zn, Cd, and Cu were studied in six, 50 cm long sediment cores. The main aim of the study was to concentrate on the history of Pb fluxes and Pb isotopic composition (²⁰⁶Pb/²⁰⁷Pb and ²⁰⁸Pb/²⁰⁶Pb) to trace Pb sources. The lowest Pb concentrations (19 μg g⁻¹) were measured in sediments deposited circa 1860, while the highest Pb concentrations (63–147 μg g⁻¹) were measured in sediments deposited between 1960s and 70s. Pre-industrial Pb fluxes were 7 Pb m² year⁻¹, while after WWII they reached 199 Pb m² year⁻¹. Highest ²⁰⁶Pb/²⁰⁷Pb ratios (∼1.22) were measured in the oldest sediment layers, and the lowest ²⁰⁶Pb/²⁰⁷Pb ratios (∼1.165) were measured in the sediments deposited in 1970s–90s. During the period of highest Pb contamination, the anthropogenic Pb fraction reached up to 93%. A general discussion of the Pb sources, emissions, and loads for Poland is included.     

Historical record of metal accumulation and lead source in the southeastern coastal region of Korea

Concentrations of heavy metals and Pb isotopes were measured in the 1-M HCl leaching fraction of core sediments spanning the last 400 years. This sedimentary record of pollution history in metal concentrations shows a good correlation with the increases in industrialization, urbanization, and energy consumption since 1901s. Notably, the Pb concentration and the ²⁰⁷Pb/²⁰⁶Pb and ²⁰⁸Pb/²⁰⁶Pb ratios were constant before the 1910s (16.7 μg/g, 0.844, and 2.098, respectively), whereas they increased steadily up to 21.9 μg/g, 0.848, and 2.101 after the 1910s. The correlations between Pb isotope ratios (²⁰⁶Pb, ²⁰⁷Pb, and ²⁰⁸Pb) showed different linear regression trends for core sediments before and after the 1910s, indicating differences in Pb sources. Our interpretation suggests that the source of anthropogenic Pb in Korean coastal region and the Yellow Sea shelf was presumed to be Chinese coals or ores, which have also played a major role as sources of atmospheric particulate Pb.     

Efficient trapping of organic carbon in sediments on the continental margin with high fluvial sediment input off southwestern Taiwan

Accumulation rates of marine and terrigenous organic carbon in the continental margin sediments off southwestern Taiwan were estimated from the measured concentrations and isotopic compositions of total organic carbon (TOC) and previously reported sedimentation rates. Surficial sediments were collected from the study area spanning from the narrow shelf near the Kaoping River mouth to the deep slope with depths reaching almost 3000 m. The average sediment loading of Kaoping River is 17 Mt/yr, which yields high sediment accumulation rates ranging from 0.08 to 1.44 g cm⁻² yr⁻¹ in the continental margin. About half of the discharged sediments were deposited on the margin within 120 km of the river mouth. Carbon isotopic compositions of terrestrial and marine end-members of organic matter were determined, respectively, based on suspended particulate matter (SPM) collected from three major rivers in the southwestern Taiwan and from an offshore station. All samples were analyzed for the TOC content and its isotopic composition (δ¹³C_org). The SPM samples were also analyzed for the total nitrogen (TN) content. TOC content in marine sediments ranges from 0.45% to 1.35% with the highest values on the upper slope near the Kaoping River mouth. The TOC/TN ratio of the SPM samples from the offshore station is 6.8±0.6, almost identical to the Redfield ratio, indicating their predominantly marine origin; their δ¹³C_org values are also typically marine with a mean of −21.5±0.3‰. The riverine SPM samples exhibit typical terrestrial δ¹³C_org values around −25‰. The δ¹³C_org values of surficial sediments range from −24.8‰ to −21.2‰, showing a distribution pattern influenced by inputs from the Kaoping River. The relative contributions from marine and terrestrial sources to sedimentary organic carbon were determined by the isotope mixing model with end-member compositions derived from the riverine and marine SPM. High fluvial sediment inputs lead to efficient trapping of organic carbon over a wide range of water depth in this continental margin. The marine organic accumulation rate ranges from 1.6 to 70 g C m⁻² yr⁻¹ with an area weighted mean of 4.2 g C m⁻² yr⁻¹, which is on a par with the mean terrestrial contribution and accounts for 2.3% of mean primary production. The depth-dependent accumulation rate of marine organic carbon can be simulated with a function involving primary productivity and mineral accumulation rate, which may be applicable to other continental margins with high sedimentation rates. Away from the nearshore area, the content of terrigenous organic carbon in surficial sediments decreases with distance from the river mouth, indicating its degradation in marine environments.     

Distribution of trace metals and Pb isotopes in bottom sediments of the Murucupi River,North Brazil

The Murucupi River belongs to the hydrographic network of the Pará River estuary, at the southern portion of the Amazon River mouth, which consists of a fluvial-marine transitional zone under strong impact of both tidal and fluvial currents. The geochemical results obtained for bottom sediments from the Murucupi River, the Arrozal Channel, and the Pará River indicate a natural variation of Pb, Cr, Cu, Zn, and Ni content among these water ways with no significant anthropogenic influence. According to the threshold effects level (TEL), the contents of trace metals do not offer risk to the local biota. By contrast, the differences in the Pb isotopic composition of sediments in the Murucupi River, the Arrozal Channel, and the Pará River are significant. These isotopic signatures indicate an anthropogenic contribution of Pb in the Murucupi River originating from the domestic effluents of urban centers; industrial waste represented by red mud is not included. These results demonstrate that the Pb isotopic signature is a prospective indicator for future contamination of bottom sediments by trace metals and is useful for identifying contaminants among the possible anthropogenic sources.     

Detection of anthropogenic Cu, Pb and Zn in continental shelf sediments off Sydney, Australia--a new approach using normalization with cobalt.

Concentrations of Co, Cu, Pb and Zn were determined in 107 surficial sediment samples from the continental margin adjacent to Sydney, Australia. The spatial distributions of trace metals in the sediments and the mud content are similar and increase with greater distance from the coast. In contrast, normalization of the concentrations of Cu, Pb and Zn in the total sediment with Co enables a coastal anthropogenic source to be identified. The spatial distribution of Co-normalized concentrations of Cu, Pb and Zn in total sediment is similar to the distribution of these trace metals in the fine fraction of sediment (<62.5 microm), indicating that Co may be used as a normalizing element for determining contaminant sources in the marine environment near Sydney.     

The atmospheric lead record preserved in lagoon sediments at a remote equatorial Pacific location: Palmyra Atoll, northern Line Islands

Anthropogenic lead (Pb) inputs to the atmosphere increased greatly over the past century and now dominate Pb supply to the oceans. However, the Pb content of sediments across the equatorial Pacific region is relatively unknown, and data exist only for deep sea sites where Pb deposition lags surface water inputs by up to a century. Here we present ICP-MS analyses of Pb of a core from a lagoon at Palmyra Atoll, northern Line Islands, that spans approximately the past 160 years. The non-bioturbated sediments of the euxinic lagoon, coupled with rapid rates of deposition, provide a unique fine-scale record of atmospheric Pb supply at a remote Pacific location. These first observations of historic Pb sedimentation in an atoll lagoon reveal a 63-fold increase in Pb flux to sediments during the past century and correlate directly with the North American consumption of leaded gasoline that began in 1926.     

Lacustrine sediments and lichen transplants: two contrasting and complimentary environmental archives of natural and anthropogenic lead in the South Urals, Russia

Lead (Pb) concentrations and isotope ratios of two different geochemical archives are compared; lake sediment cores and lichens (Hypogymnia physodes, naturally growing and transplanted) from a ca. 80 km-long transect centred on the Cu smelter and former mining town of Karabash, Ural Mountains, Russia. Lead concentrations in sediment cores from 10 lakes were generally low near their base and show an abrupt increase in their upper portions interpreted to coincide with the onset of large-scale smelting operations in 1910. Lead isotope ratios derived from ²⁰⁴Pb, ²⁰⁶Pb, ²⁰⁷Pb, ²⁰⁸Pb of the bottom layers differed significantly from those of the top. The top sediments have isotope ratios that show distinct end members, one of which was the stack dust from the Karabash smelter, which is similar to the Pb derived from ores from Sibay, a major mine in the Urals. The composition of the bottom sediment layers generally fall slightly off a mixing line between the top sediments and average Earth’s upper crust. Lichens transplanted from a reference site, as well as naturally growing lichens, sampled from southwest of the smelter have isotope ratios similar to those of the stack dust. Lichens to the northeast contained Pb from the smelter, but are increasingly influenced by other sources probably leaded petrol and local soils, and a signature derived from a source enriched in ²⁰⁷Pb. Vegetables collected from local kitchen gardens contained Pb from an additional atmospheric source, possibly coal. Our work confirms that: (1) Pb isotopes in lake sediments provide a long-term record of inputs and allows the characterisation of natural and anthropogenic sources; (2) Pb isotopes in lichens provide a short-term record of local and long-range atmospheric deposition at high spatial resolution and short time scales as they replace their Pb content within a few months; (3) determination of all four stable Pb isotopes is necessary for the identification of the sources of Pb and is extremely sensitive for discerning minor source signatures, even in an area with a dominant source such as a smelter. Particularly significant for the Karabash area is that ore-smelter-derived airborne Pb is a major component in the lake sediments and lichens but its contribution reaches insignificant levels ca. 40 km from the smelter.     

Lead isotopes in island arcs

New lead isotope data for calc-alkaline volcanic rocks from New Zealand and the Lesser Antilles, combined with published data for Japan and the Andes, show that the spread of isotopic composition in each volcanic arc region is small (2–4% range in Pb206/Pb204) compared to the range of values observed (8%). Pb207 and Pb206 increase systematically from Japan to the Andes to New Zealand to the Caribbean. Likewise Pb208 and Pb206 are positively correlated, but there is evidence of long term (10⁸ m.y.) differences of Th/U between the regions studied. The apparent U/Pb ratios of Peruvian, New Zealand and Caribbean calc-alkaline volcanics do not differ greatly from the apparent ratio for the single stage growth curve for stratiform Pb ores. In contrast the apparent U/Pb ratios for Japanese calc-alkaline volcanics are distinctly lower. Although the Japanese Pb has model ages near zero, the other volcanic arcs have negative (future) model ages, the Caribbean samples being most extreme in this respect. Published oceanic volcanic and sediment lead isotopic composition data and the new results are consistent with a model of volcanic arc evolution in which oceanic sediments are dragged into the mantle, mixed to some degree with mantle material, and partially melted to form calc-alkaline magmas. Either constant continental volume or continental growth are compatible with this process. The mixing of two separate « frequently mixed » leads is the minimum complexity required to explain volcanic are leads. Mathematically there are probably no single-stage leads but isotopic homogenization during earth history has caused lead isotopes to closely approximate a single stage growth. The use of lead isotopic composition as a « tracer » suggests that mantle — crust geochemical evolution involves an exchange of material and is not simply a one-way process. The Pb isotopic composition of the Auckland, New Zealand alkali basalts is apparently the result of incomplete mixing of two leads to give a linear array of Pb207/Pb204-Pb206/Pb204 data with negative slope.     

Chemical forms of Pb, Zn and Cu in the sediment profiles of the Pearl River Estuary

The chemical forms of heavy metals (Pb, Zn and Cu) in sediment cores of the Pearl River Estuary were studied using a sequential chemical extraction method. The isotope ratios of 206Pb/207Pb in various chemical fractions were also measured to assess the potential Pb sources. Zinc and Cu were mainly associated with the residual fraction. The Fe-Mn oxide and organic/sulphide fractions were the next important phases for Zn and Cu, respectively. For Pb, different chemical partitioning patterns were found among different sediment cores. Most Pb was associated with the residual fraction in the sediments. In some sediment profiles, the major phase of Pb in the top layers was the Fe-Mn oxide fraction. The proportion of Pb in the Fe-Mn oxide fraction decreased significantly with increasing depth. Among the different depths, the 206Pb/207Pb isotope ratios in the residual fraction remained fairly stable, with a mean value of 1.202, which may represent the natural background value. The 206Pb/207Pb ratios in the exchangeable fraction were the lowest among the five fractions, particularly in top sediments, showing the anthropogenic inputs of heavy metals from recent rapid industrial development in the surrounding region. For the other three non-residual fractions, there was a similar trend of increasing 206Pb/207Pb ratios down the profile. Results from this study are useful in assessing both the chemical changes for heavy metals in marine sediments and the potential of heavy metal release into the water environment of an estuary area.     

Trace metals in estuarine sediments from the southwestern Spanish coast

The impact of river-transported metal pollution and industrial wastes on the metal distribution (Cr, Cu, Zn, Pb) in estuarine sediments was studied in the southwestern Spanish estuaries. Intertidal and subtidal surface sediments of the Tinto-Odiel Estuary are very highly polluted by heavy metals, with geoaccumulation indices up to 4 in the three sedimentary environments studied (channel, channel border and salt marsh). The single exception is the Punta Umbria channel, very protected from the point sources by salt marsh deposits and hydraulic processes. In the remaining two estuaries, pollution (Pb, Cu) was only significant near the harbour situated in the Piedras river mouth, whereas very low values were found in the Guadiana Estuary. In these last rivers, the enrichment factor increases from the channel to the salt marsh sediments.     

Temporal evolution of lead isotope ratios in sediments of the Central Portuguese Margin: A fingerprint of human activities

Stable Pb isotope ratios (²⁰⁶Pb/²⁰⁷Pb, ²⁰⁸Pb/²⁰⁶Pb), ²¹⁰Pb, Pb, Al, Ca, Fe, Mn and Si concentrations were measured in 7 sediment cores from the west coast of the Iberian Peninsula to assess the Pb contamination throughout the last 200 years. Independently of their locations, all cores are characterized by increasing Pb/Al rends not related to grain-size changes. Conversely, decreasing trends of ²⁰⁶Pb/²⁰⁷Pb were found towards the present. This tendency suggest a change in Pb sources reflecting an increased proportion derived from anthropogenic activities. The highest anthropogenic Pb inventories for sediments younger than 1950s were found in the two shallowest cores of Cascais and Lisboa submarine canyons, reflecting the proximity of the Tagus estuary. Lead isotope signatures also help demonstrate that sediments contaminated with Pb are not constrained to estuarine–coastal areas and upper parts of submarine canyons, but are also to transferred to a lesser extent to deeper parts of the Portuguese Margin.     

Lead isotopes and trace elements in some Miocene Red Sea galenas

Summary Lead-zinc mineralization occurs in Miocene sediments along the Egyptian Red Sea Coast in several localities. Galena samples were collected from some of these localities for isotopic and trace elements studies. The isotopic ratios²⁰⁶Pb/²⁰⁴Pb,²⁰⁷Pb/²⁰⁴Pb,²⁰⁹Pb/²⁰⁴Pb for these samples indicate that they are contaminated with radiogenic lead (J-type anomalous lead) with different degrees. The variation in the degree of contamination is significant and indicates a non-uniform source of uranium and thorium from which radiogenic lead was deriven. The highst contaminations were observed in samples collected from sediments overlying or close to acidic basement rocks. The trace element content indicates that galenas were formed at low temperature from solutions that circulated the underlying basement picking several trace elements in addition to radiogenic lead.     

Source and distribution of lead in the surface sediments from the South China Sea as derived from Pb isotopes

Rapid economic development in East Asian countries has inevitably resulted in environmental degradation in the surrounding seas, and concern for the environment and its protection against pollutants is increasing. Identification of sources of contaminants and evaluation of current environmental status are essential to environmental pollution management, but relatively little has been done in the South China Sea (SCS). In order to investigate the abundance, distribution, and sources of Pb within the SCS, stable Pb isotopes and their ratios were employed to assess the contamination status and to differentiate between natural and anthropogenic origins of Pb in the surface sediments. The total Pb concentrations in sediments varied from 4.18 to 58.7 mg kg⁻¹, with an average concentration of 23.6 ± 8.9 mg kg⁻¹. The observed Pb isotope ratios varied from 18.039 to 19.211 for ²⁰⁶Pb/²⁰⁴Pb, 15.228 to 16.080 for ²⁰⁷Pb/²⁰⁴Pb, 37.786 to 39.951 for ²⁰⁸Pb/²⁰⁴Pb, 1.176 to 1.235 for ²⁰⁶Pb/²⁰⁷Pb, and 2.468 to 2.521 for ²⁰⁸Pb/²⁰⁷Pb. The majority of these ratios are similar to those reported for natural detrital materials. Combined with Pb enrichment factor values, our results show that Pb found within most of the SCS sediments was mainly derived from natural sources, and that there was not significant Pb pollution from anthropogenic sources before 1998. Further studies are needed to reconstruct deposition history and for trend analysis.     

Metals in Sediments of the Upper Laguna Madre

The Laguna Madre system is the largest hypersaline coastal basin in the United States. Surface sediments from 22 Upper Laguna Madre (ULM) sites were analyzed for grain size and metals (Cd, Cu, Ba, Cr, Mn, Ni, Pb, V, Zn, Fe, and Al) to assess the extent of contamination in the area. Sediments were found to consist mainly of sand texture. Clay and silts were minor constituents (<10%) of the sediments. Anomalies in metal concentrations were found at some sites and were related to probable sources, i.e., recreational and industrial activities. Concentrations of metals were normalized to grain size, Al, and Fe to distinguish natural and anthropogenic sources. Most metals showed positive correlations (p < 0.001) with Fe and Al, suggesting a natural variability of metal concentrations in sediments. Concentrations of metals, except Cd and Pb, at most sites were found to be below threshold concentrations thought to produce toxic effects in marine and estuarine organisms.     

Lead in corals: reconstruction of historical industrial fluxes to the surface ocean

Twentieth century environmental lead chronologies for the western North Atlantic, Pacific, and Indian Oceans have been reconstructed from annually-banded scleractinian corals. Measurements of lattice-bound Pb in sequential coral bands reveal temporal changes in surface water Pb concentrations and Pb isotopic distributions. Perturbations are observable in all specimens studied, attesting to global augmentation of environmental Pb by industrialization.In the western North Atlantic, Pb perturbations have occurred in direct response to the American industrial revolution and the subsequent introduction and phasing-out of alkyl Pb additives in gasoline. Surface ocean conditions near Bermuda may be reliably reconstructed from the coral data via a lead distribution coefficient of 2.3 for the species,Diploria strigosa. Based on²¹⁰Pb measurements, a similar distribution coefficient may be characteristic of corals in general. Surface Pb concentrations in the pre-industrial Sargasso Sea were about 15–20 pM. Concentrations rose to near 90 pM by 1923 as a result of metals manufacture and fossil fuel combustion. Beginning in the late 1940's, increased utilization of leaded gasoline eventually led to a peak concentration of 240 pM in 1971, representing an approximate 15-fold increase over background. Surface ocean concentrations are presently declining rapidly (128 pM in 1984) as a result of curtailed alkyl Pb usage. Lead isotopic shifts parallel the concentration record indicating that characteristic industrial and alkyl Pb source signatures have not changed appreciably in time. Industrial releases recorded in the Florida Keys reflect a weaker source and evidence of recirculated Pb (5–6 years old) from the North Atlantic subtropical gyre. An inferred background concentration of 38 pM suggests influence of shelf and/or resuspended inputs of Pb to these coastal waters.In remote areas of the South Pacific and Indian Oceans, industrial signals are fainter and the corals studied much younger than their Atlantic counterparts. Contemporary Pb concentrations implied by coral measurements (assumingK_D = 2.3) are 40–50 pM for surface waters near Tutuila and Galapagos in the South Pacific, and 25–29 pM near Mauritius in the Indian Ocean. A single coral band from Fiji (1920 ± 5yr) implies a pre-industrial surface water concentration of 16–19 pM Pb for the South Pacific. In view of reported surface water measurements and the North Atlantic coral data, the Pacific coral extrapolations may be slightly high. This could be a result of small variations inK_D among different coral genera, or incorporation of diagenetic Pb by corals sampled in coastal environments.