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1.
Concentrations of lead were measured in a surface transect and at two vertical profile stations (15°N and 20°S) in the Central Pacific. These measurements complement similar measurements made earlier in the North Pacific at 33°N and in the Northwest Atlantic at 34°N [1,2], as well as recent measurements of eolian lead input fluxes near each of these locations [3]. The new transect of surface water concentrations of lead corroborates previous measurements, which decrease from 13 ng/kg at 30°N to 4 ng/kg at 17°S in the Central Pacific [4]. This transect gradient is shown to overlie a similar geographic gradient of subsurface maximum concentrations of lead in the three Pacific vertical profile stations, decreasing from 14 ng/kg at 33°N to 11 ng/kg at 14°N to 2.5 ng/kg at 20°S. Lead concentrations at each of those locations exhibit maxima at 400 m, decreasing concentrations to 2500 m and approximately concentrations of 0.8–1.1 ng/kg below that depth. The subsurface maximum at the northwest Atlantic profile station (36 ng/kg at 34°N) is also congruent with surface water lead concentrations which decrease from 806 ng/kg to 32 ng/kg in an offshore transect from Rhode Island to 34°N, 66°W [5], and the shape of the Atlantic profile is congruent with those in the Pacific. There is a positive correlation between the magnitudes of eolian lead input fluxes and the magnitudes of the upper water maxima in lead concentration profiles at corresponding locations as follows: South Pacific easterlies 3 ng/cm2 yr vs. 2.5 ng/kg; North Pacific easterlies 6 ng/cm2 yr vs. 11 ng/kg; North Pacific westerlies 50 ng/cm2 yr vs. 14 ng/kg; and North Atlantic westerlies 170 ng/cm2 yr vs. 36 ng/kg.This relationship enables one to view the anthropogenic perturbations of the marine lead cycle on a global scale, since the industrial origin of eolian and seawater lead has been established by correlations between geographic patterns of industrial lead emissions to the atmosphere and isotopic ratios of industrial leads [3] and by geographic patterns of Pb/silicate-dust ratios and lead isotopic ratios in ocean surface waters [3–5]. These new data coupled with earlier biogeochemical data indicate that surface water concentrations of lead in the North Pacific and North Atlantic are now conservatively estimated to be 8 to 20-fold greater and those in the South Pacific are 2-fold greater than natural concentrations because of industrial emissions of lead to the atmosphere.  相似文献   

2.
Vertical profiles of Cd, Zn, Ni, and Cu have been determined at three stations in the North Pacific and in the surface waters on a transect from Hawaii to Monterey, California. The distributions found are oceanographically consistent and provide a needed confirmation and extension of several recent studies on the marine geochemistries of these metals. Cadmium concentrations average 1.4 pmol/kg in surface waters of the central North Pacific and show a strong correlation with the labile nutrients, phosphate and nitrate, increasing to values of 1.1 nmol/kg at depths corresponding to the phosphate maximum. Zinc is depleted in surface waters of the central gyre to an average value of 0.07 nmol/kg and increases to a deep maximum of 9 nmol/kg exhibiting a strong correlation with the nutrient silicate. Nickel concentrations average 2.1 nmol/kg in surface central gyre waters and increase to a deep maximum of 11 nmol/kg. Nickel is best correlated with a combination of phosphate and silicate. Copper averages less than 0.5 nmol/kg in surface waters of the central North Pacific and increases gradually to values of 5 nmol/kg in bottom waters. The Cu profiles show evidence of intermediate and deep water scavenging. The involvement of these metals in the internal biogeochemical cycles of the sea is responsible for their distributions which are predictable on the basis of oceanographic parameters.  相似文献   

3.
The general form of Cu-depth profiles is unique. In the central North Pacific, values decrease from a surface maximum of about 3 nmol/kg to 1.5 nmol/kg in the upper thermocline. Below about 750 m there is an increase to over 6 nmol/kg in the bottom waters with no mid-depth extremum. The profiles in the boundary regions are similar in the deep water but do not have the surface maximum. This unique elemental distribution is maintained by aeolean input to the surface waters comparable in magnitude to the fluvial component, ubiquitous scavenging in the subsurface and deep water, and a strong bottom source. Apparently the scavenging agent, presumably sinking particles, loses its Cu-binding capacity during early diagenesis. The half-life with respect to scavenging is about 1100 years and the overall residence time with respect to input or final removal about 5000 years.  相似文献   

4.
Manganese in the North Pacific   总被引：1，自引：0，他引：1  
A quantitative and precise method for determination of dissolved Mn at the nanomole(nmol)/kg level in seawater has been developed and used to study the distribution of Mn in the northeast Pacific. Mn concentrations in the surface mixed layer decrease from 1.0 to 0.6 nmol/kg between the central gyre and the western boundary of the California Current, then increase to values from 2 to 6 nmol/kg near the coastal boundary (in contrast to the distribution of210Pb). Particulate Mn in the surface waters accounts for only about 1% of the total.Vertical distributions of Mn are characterized by surface maxima, minima near 300 m, maxima at mid-depth coinciding with the oxygen minimum and the labile nutrient maxima, and concentrations in Pacific bottom waters of approximately 0.2 nmol/kg. The oceanic distribution of Mn appears to be dominated by external inputs superimposed upon overall scavenging which can lead to Mn maxima in (1) the surface waters due to riverine and atmospheric sources; (2) the deep ocean as a result of hydrothermal injection and/or sediment resuspension; and (3) the oxygen minimum region resulting from in-situ breakdown of organic matter, in-situ MnO2 reduction, and/or advective-diffusive transport of dissolved Mn from anoxic slope sediments.  相似文献   

5.
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 (assumingKD = 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 inKD among different coral genera, or incorporation of diagenetic Pb by corals sampled in coastal environments.  相似文献   

6.
226Ra and Ba show a general linear correlation in the oceanic water column within the uncertainties of the data: the slope of the line is about 4.6 nanomoles (nmoles) Ra/mole Ba, the intercept being at about 4 nmoles Ba/kg. This demonstrates the usefulness of Ba as a “chemical analogue” of Ra. Box-model calculations indicate that the average deep-water excess of Ra over Ba should be about 10% relative to the surface. This is consistent with the observations outside the deep northeast Pacific. However, the uncertainties in the data are such that the regional variation in the primary input cannot be resolved. In the deep waters of the North Pacific there is in fact a large excess of Ra relative to Ba. The one detailed profile presently available (204) can be explained consistently by a simple vertical advection-diffusion model.  相似文献   

7.
Nickel has been measured on four Geosecs profiles from the Atlantic and Pacific. The resulting distribution is oceanographically consistent: the concentration levels are over a factor of five lower than any previously reported. Values range from as low as 3 nmoles/kg in surface waters to 12 nmoles/kg in the deep North Pacific. The form of the Pacific profiles indicates that nickel is involved in the biogeochemical cycle and is regenerated both at shallow depths, like phosphate and in the deep waters like silicate. The oceanic residence time is ca. 10,000 years. While ferromanganese phases may be the ultimate sink for nickel they do not control its distribution in the water column.  相似文献   

8.
The thorium isotope content of ocean water   总被引：1，自引：0，他引：1  
232Th concentrations of surface and deep Pacific Ocean waters are 0.01–0.02 dpm/1000 kg (60 pgm/kg). The230Th activity is 0.03–0.13 dpm/1000 kg in surface waters and 0.3–2.7 dpm/1000 kg in deep waters. Chemical residence times based on in situ production from parent isotopes are about the same for230Th and228Th in surface waters (1–5 years) but are ten times greater for230Th in deep waters (10–100 years). Apparently there are additional sources of230Th into deep waters. At MANOP site S manganese nodule tops are enriched in Th isotopes by adsorption of Th from seawater and not by incorporation of Th-rich particulates.  相似文献   

9.
In the study, we establish centennial records of anthropogenic lead pollution at different locations in the North Atlantic (Iceland, USA, and Europe) by means of lead deposited in shells of the long-lived bivalve Arctica islandica. Due to local oceanographic and geological conditions we conclude that the lead concentrations in the Icelandic shell reflect natural influxes of lead into Icelandic waters. In comparison, the lead profile of the US shell is clearly driven by anthropogenic lead emissions transported from the continent to the ocean by westerly surface winds. Lead concentrations in the European North Sea shell, in contrast, are dominantly driven by local lead sources resulting in a much less conspicuous 1970s gasoline lead peak. In conclusion, the lead profiles of the three shells are driven by different influxes of lead, and yet, all support the applicability of Pb/Ca analyses of A. islandica shells to reconstruct location specific anthropogenic lead pollution.  相似文献   

10.
The Indonesian Throughflow (ITF) links upper ocean waters of the west Pacific and Indian Ocean, modulates heat and fresh water budgets between these oceans, and in turn plays an important role in global climate change. The climatic phenomena such as the East Asian monsoon and El Niño-Southern Oscillation (ENSO) exert a strong influence on flux, water properties and vertical stratification of the ITF. This work studied sediments of Core SO18462 that was retrieved from the outflow side of the ITF in the Timor Sea in order to investigate response of the ITF to monsoon and ENSO activities since the last glacial. Based on Mg/Ca ratios and oxygen isotopes in shells of planktonic foraminiferal surface and thermocline species, seawater temperatures and salinity of both surface and thermocline waters and vertical thermal gradient of the ITF outflow were reconstructed. Records of Core SO18462 were then compared with those from Core 3cBX that was recovered from the western Pacific warm pool (WPWP). The results displayed that similar surface waters occurred in the Timor Sea and the WPWP during the last glacial. Since ～16 ka, an apparent difference in surface waters between these two regions exists in salinity, indicated by much fresher waters in the Timor Sea than in the WPWP. In contrast, there is little change in difference of sea surface temperatures (SSTs). With regard to thermocline temperature (TT), it increased until ～11.5 ka since the last glacial, and then remained an overall unchanged trend in the WPWP but continuously decreased in the Timor Sea towards the late Holocene. Since ～6 ka, thermocline waters have tended to be close to each other in between the Timor Sea and the WPWP. It is indicated that intensified precipitation due to East Asian monsoon and possible ENSO cold phase significantly freshened surface waters over the Indonesian Seas, impeding the ITF surface flow and in turn having enhanced thermocline flow during the Holocene. Consequently, thermocline water of the ITF outflow was cooling and thermocline was shoaling towards the late Holocene. It is speculated that, in addition to strengthening of East Asian winter monsoon, increasing ENSO events during the late Holocene likely played an important role in influencing thermocline depth of the ITF outflow.  相似文献   

11.
Thermoplastic resin pellets are melted and formed into an enormous number of inexpensive consumer goods, many of which are discarded after a relatively short period of use, dropped haphazardly onto watersheds and then make their way to the ocean where some get ingested by marine life. In 2003 and 2004 pre-production thermoplastic resin pellets and post-consumer plastic fragments were collected and analyzed for contamination for persistent organic pollutants (POPs). Samples were taken from the North Pacific Gyre, and selected sites in California, Hawaii, and from Guadalupe Island, Mexico. The total concentration of PCBs ranged from 27 to 980 ng/g; DDTs from 22 to 7100 ng/g and PAHs from 39 to 1200 ng/g, and aliphatic hydrocarbons from 1.1 to 8600 microg/g. Analytical methods were developed to extract, concentrate and identify POPs that may have accumulated on plastic fragments and plastic pellets. The results of this study confirm that plastic debris is a trap for POPs.  相似文献   

12.
226Ra data on eleven vertical profiles taken during the GEOSECS program from the Antarctic Ocean and its vicinity in both the Atlantic and the Pacific are presented. Replicate measurements were made on each sample using the Rn-emanation method. The precision (1 σ) based on triplicate analyses averages about ±2.5%. Waters all around the Antarctic continent below 2 km depth appear to exhibit a uniform226Ra concentration of 21.5 ± 1dpm/100kg, except perhaps locally such as the Ross Sea and the Drake Passage where small variations may be present. Higher in the water column, the226Ra contents decrease toward the surface with gradients which vary as a function of the influence exerted by the Antarctic Convergence. Across this oceanic front, a north-to-south increase of226Ra occurs (the increase being the largest near the surface: from 8 to 18 dpm/100 kg), reflecting the combining effect of deep-water upwelling and meridional water mixing. The core layer of the Antarctic Intermediate Water contains about 14 dpm/100 kg of226Ra and that of the Circumpolar Intermediate Water (O2 minimum and local T maximum) about 18 dpm/100 kg. To a first approximation,226Ra covaries with Si in the circumpolar waters.  相似文献   

13.
Profiles of nonylphenol isomers in surface waters from Sri Lanka   总被引：1，自引：0，他引：1  
Isomer-specific concentrations of nonylphenol (NP) and their predicted estrogenic potency were investigated in Sri Lankan waters for the first time. The total concentration of 13 NP isomers ranged from 90 to 1835 ng/L, while the predicted estrogenic equivalent concentration ranged from 0.072 to 1.38 ng 17β-estradiol (E2)/L. Bire Lake, located in the central area of the commercial capital, Colombo, had the highest contamination among the studied locations. These data show that NP levels in Sri Lankan waters are well within the recently reported concentrations in other regions of the world. The spatial differences in NP concentrations suggest that NP contamination in Sri Lanka may be widespread, and comprehensive study is vital.  相似文献   

14.
228Ra concentrations were measured in 12 subsurface water samples collected during August–September 1970 in the North Atlantic at the Second Geosecs Intercalibration Station.228Ra concentrations ranged from 1.5 to 2.1 dpm/100 kg in the water layer between 100 and 600 m depth, above the main thermocline, but decreased with increasing depth to less than 0.5 dpm/100 kg at 1.5 km, below the main thermocline. The two deepest samples, collected below 4 km depth, indicated that the228Ra concentration increased again to at least 1.2 dpm/100 kg as the interface with the sea floor sediments was approached. Above the 4 km level, the228Ra profile was roughly similar to the tritium profile measured by Roether and Münnich.  相似文献   

15.
Organochlorine (OCs) and butyltin (BTs) residues were determined in deep-sea organisms collected from the western North Pacific, off-Tohoku, Japan. Among OCs, concentrations of polychlorinated biphenyls (PCBs) and DDTs (DDTs and its metabolites) were the highest in deep-sea organisms (maximum concentrations of 6700 and 13,000 ng/g lipid wt, respectively). Chlordane compounds (CHLs) were the next most abundant OCs, and hexachlorocyclohexanes (HCHs) and hexachlorobenzene (HCB) were the lowest. BTs were also detected at maximum concentrations of 570 ng/g wet wt. Concentrations of PCBs, CHLs and BTs in deep-sea organisms collected from the western North Pacific, off-Tohoku, were generally lower than those in deep-sea and shallow water organisms from Japanese coastal waters. On the other hand, considerable variations in the concentrations of OCs were found among deep-sea organisms analyzed. Several carnivorous fishes such as snubnosed eel, lanternshark and grenadiers accumulated some OCs such as PCBs, DDTs and CHLs at high concentrations of up to a few μg/g levels. In addition, the residue pattern of OCs and BTs in fishes showed a specific trend according to the sampling depth; higher concentrations of PCBs, DDTs and CHLs and lower concentrations of HCHs, HCB and BTs were found in fishes collected from greater depth (1000 m) compared to those from shallower waters. This trend is consistent with the results of our earlier study on mesopelagic myctophid fishes. Results of this study suggest vertical transport of hydrophobic OCs such as PCBs, DDTs and CHLs and its accumulation in benthic deep-sea organisms.  相似文献   

16.
Lead accumulates in shallow salt marsh sediments and is taken up by grasses. Since about half of the annual grass crop is transported to the sea after the grass dies, this may contribute to the movement of lead to deeper waters. Where nitrogen additions increase the biomass of grasses, or where very heavy lead contamination takes place, substantial amounts of lead may be removed by tides from the marsh surfaces.  相似文献   

17.
Water sampling during the 1993 IV Russian–US Joint Expedition to the Bering and Chukchi Seas (BERPAC) indicates that Pacific Ocean burdens of the long-lived radionuclide 129I are relatively low in the Pacific-influenced Arctic, particularly compared to high latitude waters influenced by the North Atlantic. These low concentrations occur despite the presence of potential submerged anthropogenic sources in the East Sea (Sea of Japan), and in the northwest Pacific Ocean, east of the Kamchatka Peninsula. The concentration of 129I entering the Arctic Ocean through Bering Strait, 0.7×108 atoms kg−1, is only slightly higher than observed in deep Pacific waters. Similar concentrations (0.44–0.76×108 atoms kg−1) measured in Long Strait indicate no significant transfer of 129I eastward into the Chukchi Sea in the Siberian Coastal Current from the Siberian marginal seas to the west. However, the concentrations reported here are more than an order of magnitude higher than the Bering Strait input concentration estimated (1.0×106 atoms kg−1) from bomb fallout mass balances, which supports other existing evidence for a significant atmospheric deposition term for this radionuclide in surface ocean waters. Near-bottom water samples collected in productive waters of the Bering and Chukchi Seas also suggest that sediment regeneration may locally elevate 129I concentrations, and impact its utility as a water mass tracer. As part of this study, two deep 129I profiles were also measured in the East Sea in 1993–1994. The near-surface concentration of 129I ranged from 0.12 to 0.31×108 atoms kg−1. The 129I concentration showed a steady decrease with depth, although because of active deep water ventilation, the entire 3000 m water column exceeded natural concentrations of the radionuclide. Atom ratios of 129I/137Cs in the East Sea also suggest an excess of 129I above bomb fallout estimates, also possibly resulting from atmospheric deposition ultimately originating from nuclear facilities.  相似文献   

18.
Anthropogenic mercury pollution was studied in Kastela Bay (Croatia), 10 years after chloralkaline plant (PVC) stopped production. The concentration of total mercury determined in sediments which are composed mainly of calcite and quartz, are in the range 14,280-30,400 ng/g. The values are higher than reported in the literature for Elbe and Seine estuaries and also above 25,000 ng/g used for criterion in remediation project in Minamata Bay. The concentration of methylmercury 6.05-36.74 ng/g are typical for slightly to highly contaminated estuarine sediments. The low ratio of methylmercury to total mercury found in sediments of Kastela Bay is in the range 0.04-0.18%. It can be explained that in this region predominate conditions which do not promote in-situ methylation. Sediments were found to be highly anoxic. Concentrations of total mercury in unfiltered surface waters are in the range 69-145 ng/l and in unfiltered bottom waters in the range 230-1,418 ngl(-1). High concentrations found in bottom waters suggest that either resuspension or partial dissolution of sediments takes place. An experiment performed on filtered and unfiltered waters showed that about 85% of total mercury in surface water and almost 100% in bottom water was retained on 45 microm filters. To demonstrate contrasts, two pristine estuaries from norths and south Europe were studied. Silicious sediments of Ore estuary (Sweden) and calcareous sediments of Krka estuary (Croatia) have total mercury concentrations close to accepted background level. The ratio of methylmercury to total mercury is < or = 1% in all samples with one exception. The highest observed ratio (2.70%) was in the surface sediment from E2 station in Krka estuary measured in March 2000. This location is suitable for studying methylmercury formation in pristine environment.  相似文献   

19.
Low level hydrocarbon contamination is measurable in the vicinity of Antarctic stations, N-alkane and polycyclic aromatic hydrocarbon (PAH) concentrations in seawater and sediment at Signy Station, South Orkney Islands indicated contamination was confined to within a few hundred metres of the station. Total n-alkane concentrations in seawater decreased from 7.6 to 2.6 μg l−1 within 500 m of the station. All n-alkane values in seawater were within the limits of variation for oceanic waters proposed by cripps (1992), although the distribution pattern suggested pollution from the station. The total PAH concentration in seawater varied between 110 and 216 ng l−1. These values showed no trend with distance from the station and were all slightly higher than for the open ocean. The n-alkane and PAH concentations in the surface sediment declined to low levels within 375 m of the station. This indicates that a large proportion of the hydrocarbons entering Factory Cove was deposited from the water column. Sediment n-alkane concentrations were similar at all depths of the cores when collected more than 125 m from the station. PAH levels in the sediment appeared to be due to local input, including a small spill in 1965.  相似文献   

20.
The use of antifouling paints to the boats and ships is one among the threats facing coastal resources including coral reefs in recent decades. This study reports the current contamination status of diuron and its behaviour in the coastal waters of Malaysia. The maximum concentration of diuron was 285 ng/L detected at Johor port. All samples from Redang and Bidong coral reef islands were contaminated with diuron. Temporal variation showed relatively high concentrations but no significant difference (P > 0.05) during November and January (North-East monsoon) in Klang ports (North, South and West), while higher levels of diuron were detected during April, 2012 (Inter monsoon) in Kemaman, and Johor port. Although no site has shown concentration above maximum permissible concentration (430 ng/L) as restricted by the Dutch Authorities, however, long term exposure studies for environmental relevance levels of diuron around coastal areas should be given a priority in the future.  相似文献   

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