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1.
Surface pelagic tar concentrations in the equatorial South Atlantic Ocean were low (< 0.001 to 14.6 mg m?2). With one exception, concentrations were less than 0.5 mg m?2. The tars were characterized by gravimetry, carbon isotopic composition, molecular compositions (gas chromatographically), sulphur content, total fluorescence spectra, and biological marker fingerprints. Most tars exhibited significant amounts of degradation. A total fluorescence technique was used to group the tars into two basic types. One type occurred at low concentrations and appeared to be due to chronic long-term oil pollution in the South Atlantic Ocean. The second group occurred at much higher concentrations and was associated with more coastal-influenced waters. Biological marker (triterpanes and steranes) fingerprints confirmed the fluorescence groupings. Carbon isotopic composition and pristane/phytane ratios exhibited few geographical trends.  相似文献   

2.
This study provides data concerning the hydrography and water chemistry of the Atlantic region between 29-38° N and 27-31° W, and establishes background values for dissolved Cu, Cd, Pb and As. Three water masses were identified: the Eastern North Atlantic Central Water (ENACW), the Mediterranean Water (MW) and the North Atlantic Deep Water (NADW). The ENACW exhibits a clear meridional gradient of temperature and salinity, with comparatively high values at the southern sites and lower values on the Azores platform. The ENACW, which includes the euphotic zone, also had comparatively high concentrations of oxygen and lower concentrations of nutrients and metals. The Cu, Cd and Pb results suggest that new background concentrations for OSPAR Region V (the Wider Atlantic) should be established as follows: 0.15-13nM for Cu, 0.05-1.4nM for Cd and 0.03-5nM for Pb. The background concentrations of As for OSPAR Region V should be 7-28nM.  相似文献   

3.
Coastal rivers represent a significant pathway for the delivery of natural and anthropogenic sediment‐associated chemical constituents to the Atlantic, Pacific and Gulf of Mexico coasts of the conterminous USA. This study entails an accounting segment using published average annual suspended sediment fluxes with published sediment‐associated chemical constituent concentrations for (1) baseline, (2) land‐use distributions, (3) population density, and (4) worldwide means to estimate concentrations/annual fluxes for trace/major elements and total phosphorus, total organic and inorganic carbon, total nitrogen, and sulphur, for 131 coastal river basins. In addition, it entails a sampling and subsequent chemical analysis segment that provides a level of ‘ground truth’ for the calculated values, as well as generating baselines for sediment‐associated concentrations/fluxes against which future changes can be evaluated. Currently, between 260 and 270 Mt of suspended sediment are discharged annually from the conterminous USA; about 69% is discharged from Gulf rivers (n = 36), about 24% from Pacific rivers (n = 42), and about 7% from Atlantic rivers (n = 54). Elevated sediment‐associated chemical concentrations relative to baseline levels occur in the reverse order of sediment discharges: Atlantic rivers (49%) > Pacific rivers (40%) > Gulf rivers (23%). Elevated trace element concentrations (e.g. Cu, Hg, Pb, Zn) frequently occur in association with present/former industrial areas and/or urban centres, particularly along the northeast Atlantic coast. Elevated carbon and nutrient concentrations occur along both the Atlantic and Gulf coasts but are dominated by rivers in the urban northeast and by southeastern and Gulf coast (Florida) ‘blackwater’ streams. Elevated Ca, Mg, K, and Na distributions tend to reflect local petrology, whereas elevated Ti, S, Fe, and Al concentrations are ubiquitous, possibly because they have substantial natural as well as anthropogenic sources. Almost all the elevated sediment‐associated chemical concentrations found in conterminous US coastal rivers are lower than worldwide averages. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

4.
Seabirds aggregate around oil drilling platforms and rigs in above average numbers due to night lighting, flaring, food and other visual cues. Bird mortality has been documented due to impact on the structure, oiling and incineration by the flare. The environmental circumstances for offshore hydrocarbon development in North-west Atlantic are unique because of the harsh climate, cold waters and because enormous seabird concentrations inhabit and move through the Grand Banks in autumn (storm-petrels, Oceanodroma spp), winter (dovekies, Alle alle, murres, Uria spp), spring and summer (shearwaters, Puffinus spp). Many species are planktivorous and attracted to artificial light sources. Most of the seabirds in the region are long-distance migrants, and hydrocarbon development in the North-west Atlantic could affect both regional and global breeding populations. Regulators need to take responsibility for these circumstances. It is essential to implement comprehensive, independent arm's length monitoring of potential avian impacts of offshore hydrocarbon platforms in the North-west Atlantic. This should include quantifying and determining the nature, timing and extent of bird mortality caused by these structures. Based on existing evidence of potential impacts of offshore hydrocarbon platforms on seabirds, it is difficult to understand why this has not been and is not being, systematically implemented.  相似文献   

5.
The particulate concentrations of 17 trace metals, Al, Sc, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Se, Ag, Sb, Au, Hg, Pb and Th have been measured in the marine atmosphere (58 samples) and in the deep waters (35 samples) of the Tropical North Atlantic. For oceanic suspended matter, our results are similar to those in samples from the Atlantic and the Pacific Oceans collected during the GEOSECS Program. Based on these results, we have made a flux balance for the mixed layer between input via the atmosphere and removal through small and large particles. These data show that the primary flux of suspended aluminosilicates in the Tropical North Atlantic is attributable to the atmospheric input. Elements Sc, Th, Fe, V, Mn, Co and Cr show high correlation with Al in the marine atmosphere. Of these elements, Fe, Mn, V, Co and Cr are influenced by additional processes such as biological, in the marine environment. For elements Ni, Cu, Zn, Se, Ag, Sb, Au, Hg and Pb, we observe high enrichments (relative to average crustal material) in the marine atmosphere which may be due, at least partially, to the influence of anthropogenic sources. These metals also show similar enrichments in deep ocean suspended matter. Model calculations indicate that the atmospheric flux may not control the deep ocean particulate chemistry of Ni, Cu, Zn, Ag, Sb, Au and Hg. Hence it is likely that, for these elements, the enrichment in the ocean is due to processes within the marine regime, for example their involvement in the biological cycle of the ocean. For Se and Pb, the atmospheric source looks to be the dominant contribution to their particulate concentration in seawater. In the deep North Atlantic, particulate Pb appears to be mostly of anthropogenic origin, which is not the case for Se.  相似文献   

6.
This study presents the distribution of dissolved inorganic carbon (DIC) along the Strait of Gibraltar, its tidal-induced variability, as well as the inorganic carbon exchange between the Atlantic Ocean and Mediterranean Sea. During November 2003, water column samples were collected at nine stations to measure total alkalinity (TA), pH, and dissolved oxygen (DO) for the spatial characterization of the carbonate system. At the same time, anchored samplings were carried out, above the Camarinal Sill and in the Eastern Section of the Strait, in order to assess the tidal mixing effects for oxygen and DIC distribution on the water column. Three distinct water masses can be discerned in this area: the Surface Atlantic Water (SAW), the Mediterranean Water (MW), and the less abundant North Atlantic Central Water (NACW). The observations show an increase in the DIC and a decrease in oxygen concentration with depth, related to the different physico-chemical features of each water mass. The results show the high time-dependence of the vertical distribution of DIC with the interface oscillation, affected by the intense mixing processes taking place in the Strait. Intense mixing episodes over the Camarinal Sill are responsible for an increase in the DIC concentrations in the upper layer of the Eastern Section of the Strait. Higher DIC concentrations in the Mediterranean than in the Atlantic waters are responsible for a net DIC transport of 1.47×1012 mol C yr−1 to the Atlantic Ocean. Nevertheless, the net exchange is highly sensitive to the interface definition, as well as to the estimate of water volume transport used.  相似文献   

7.
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   

8.
This study aimed at comparing toxic element (Hg, Cd) bioaccumulation in relation to age for bottlenose (Tursiops truncatus) and striped dolphins (Stenella coeruleoalba) from Mediterranean and Atlantic waters. Metal concentrations were also measured in selected prey to infer metal exposure through the diet. As expected, Mediterranean prey exhibited the highest Hg levels, probably as a consequence of the Hg enrichment of the Mediterranean Sea. Comparing the predators from each area and taking age into account, Mediterranean bottlenose dolphins displayed higher Hg levels than Atlantic dolphins (p = 0.032), whereas Mediterranean striped dolphins did not (p = 0.691). The consumption of Myctophid fish, which showed the highest Hg levels (105+/-80 ngg(-1) w.wt.) among Atlantic prey, may explain the high Hg levels in the liver of the Atlantic striped dolphins and suggested a preferential offshore feeding behaviour in this area. Concerning Cd, no clear differences were found between geographical areas.  相似文献   

9.
The monitoring programme of harmful substances in selected species in the Baltic Sea was started in 1979. In the present study, three-year averages of Zn, Cu, Cd and Pb in cod liver (Hg in cod muscle) and herring muscle are reported. The concentrations of heavy metals in cod show areal differences roughly in accordance with the concentrations of heavy metals in sea water. No significant differences between heavy metal concentrations in North Atlantic and Baltic Sea species were found, except for mercury, for which values in the Baltic Sea species are lower than in those from the North Atlantic.  相似文献   

10.
The effect of crab beds and bioturbation activity of the SW Atlantic intertidal crab Chasmagnathus granulata on the organochlorine pesticide (OCP) concentrations in Bahía Blanca estuary, Argentina were studied. Total OCP concentration was significantly lower inside than outside the crab burrows. Nevertheless, the concentrations from outside the crab beds were lower than from outside crab burrows, which indicated that crab beds act as sinks of sediment-bound OCP due to the bioturbation activities of the crabs. The same distribution patterns were found in all sediments as well as in crabs, being cyclodienes>HCHs>DDTs, although large amounts of metabolites rather than the respective parental were found in the organism showing the capacity of C. granulata for metabolising parental compounds. These more water-soluble compounds are excreted by the faeces and finally removed by tidal flushing to the sea. Our results suggest that crabs when present play a role in the distribution of sediment-bound OCP and the crab beds are modifiers of the dynamic of organic pollutants in estuarine areas.  相似文献   

11.
The concern about emerging contaminants such as pharmaceuticals is growing, mainly due to the increased global consumption of synthetic chemicals and the potential risk to environmental and human health. Although developing countries may be hotspots of pharmaceutical pollution, the knowledge about the occurrence of pharmaceuticals is still limited and patchy. Brazil holds one of the largest freshwater volumes globally, yet, little is known about the occurrence of pharmaceuticals in reservoirs although they make up key water sources. The aim of this study was, therefore, to investigate micropollutant occurrence, mainly pharmaceuticals, in four freshwater reservoirs distributed in Brazil. Water samples were collected in the Curuá-Una (CUN, Amazon region), Chapéu D’Uvas (CDU, Atlantic Forest region), Funil (FUN, Atlantic Forest region), and Simplício (SIM, Atlantic Forest region) reservoirs. The occurrence of 28 different micropollutants, including 26 pharmaceuticals, was investigated with target analysis on a UHPLC-Orbitrap-MS/MS, and a non-target screening approach was performed on all water samples to identify the presence of additional contaminants. The highest micropollutant concentrations were observed in FUN and SIM, which are the reservoirs with the largest population size in the catchment. Only caffeine was detected in CDU and CUN, which are reservoirs less influenced by urbanization. Metformin was the pharmaceutical with the highest concentrations, reaching 2 191 ng L−1 in FUN. The non-target screening identified 125 chemicals, of which most were pharmaceuticals. The numbers of compounds identified and which were above the LOQ were higher in FUN and SIM, in agreement with results from the target analysis. Metformin is the compound with the highest risk to affect FUN reservoir negatively, based on calculated risk quotients. Considering that the reservoirs are used for multiple purposes, including water supply, irrigation, and aquaculture, it is important to continue investigating micropollutant occurrence to guarantee environmental and human health.  相似文献   

12.
We have determined the dry weight of suspended particulate matter in seawater in a section through the western Atlantic Ocean from 75°N to 52°S. The concentrations, operationally defined as that weight retained on 0.6-μm and 0.4-μm pore size Nuclepore filters, contained in 1 kg of seawater, range from 5 to 300 μg/kg and show readily explainable regional features. High concentrations are found in surface waters and in association with radpidly moving bottom waters in the Denmark Straits overflow and in Antarctic bottom waters to 15°S. Low concentrations, <12 μg/kg, characterize the mid-water regions of the sub-tropical gyres. High concentrations are seen in sinking Labrador Sea water and in a plume extending at least a kilometer off the bottom at 35°N–40°N where the cruise track intersects the North Atlantic gyre. It is doubtful whether this important phenomenon could be observed by any means other than through particulate observations, either optical or gravimetric, and this provides a unique insight into the scale of vertical turbulent processes.  相似文献   

13.
Areal distributions and complete time histories since 1952 are presented of the tritium and90Sr concentrations in North Atlantic surface water. The distributions are based on a compilation of measured North Atlantic surface water tritium concentrations which is part of this paper and includes hitherto unpublished measurements, and on available90Sr compilations. To reconstruct the insufficiently represented early concentrations, a two-box North Atlantic mixing model with tropospheric input is employed, for which the input is specified (on relative scales), and which is fitted to the available surface water observations. This procedure gives a natural tritium concentration of 0.2 TU (±30%), and furthermore suggests that part of the old oceanic tritium and90Sr measurements are high. The fit requires characteristic model mixing times of 2.5 years (exchange with an intermediate-depth reservoir about three times the size of the surface box) and 30 years (loss into the deep ocean), and a tritium/90Sr input ratio of 310 Ci/Ci. The areal distributions and time histories can serve as boundary value data for evaluations of subsurface tritium and90Sr measurements.  相似文献   

14.
This paper contains a comparative analysis of the theoretical parameters involved in the subsidence of spreading ridges into the asthenosphere: Reykjanes, Kolbeinsey, the Azores segment of the Mid-Atlantic Ridge, as well as the following aseismic ridges: the Ninety East Ridge, Maldives, Hawaiian-Emperor, and Louisville ridges due to the influence of a mantle plume. We conclude that the respective geodynamic processes involved in generating spreading ridges in the North Atlantic and the aseismic ocean ridges due to hotspot action are similar. The main phases in the evolution of the Iceland region are substantiated using geological and geophysical data and computer simulation. We discuss the Cenozoic tectonic evolution of the region, calculated and plotted paleogeodynamic reconstructions of the North Atlantic Ocean in the hotspot system for 60, 50, and 20 Ma.  相似文献   

15.
3/He4He measurements at two stations in the Atlantic show that the deep water (> 2 km) contains far less excess3He than our previous measurements have shown for the Pacific Ocean. The3/He4He ratio anomaly (relative to atmospheric3/He4He) is approximately 5% for the deep Atlantic compared to about 20% for the deep Pacific. The North Atlantic3He profile shows much more structure than the South Atlantic profile, with maxima observed at 500 m, 1900 m, and 3200 m. The maxima at 500 m and 1900 m are probably due to in situ tritium decay, whereas the 3200 m maximum cannot be due to tritium, and is probably due to leakage of3He into the Atlantic water from the mantle. It seems significant that maxima in the trace elements Cu, Zn and Fe have also been observed at 3200 m at this station by Brewer, Spencer and Robertson.  相似文献   

16.
Measurements of 231Pa, 230Th and 232Th concentrations have been made on five water-column profiles along the western margin of the Madagascar and Mascarene Basins in the southern Indian Ocean. These measurements help to fill a significant gap in the global coverage of water-column 232Th, 230Th and 231Pa data. 232Th concentrations vary, but generally increase with depth, suggesting higher particle loading in deeper waters, and the presence of a significant dissolved fraction of 232Th. 230Th concentrations increase with depth, and profiles are similar to the average of existing data from other regions. 231Pa concentrations, on the other hand, show significant depth structure, apparently reflecting the various water masses sampled at this location. The modified remnants of North Atlantic Deep Water are found at a depth of ≈ 2000 m and exhibit elevated 231Pa concentrations exported from the South Atlantic. Antarctic Intermediate and Bottom Waters have lower 231Pa, probably due to scavenging onto opal particles during transit from the Southern Ocean. The differences between water masses raises a question: which water mass is important in controlling the 231Pa/230Th ratio in underlying sediments? A simple one-dimensional model is used to demonstrate that the 230Th and 231Pa exported to sea-floor sediments last equilibrates with waters close to the seafloor (within ≈ 1000 m), rather than averaging the whole water column. These findings suggest that 231Paxs/230Thxs in sediments provides information primarily about deep-water masses. In this region, sedimentary records will therefore provide information about the past flow of Antarctic Bottom Water into the Indian Ocean. Interpretation of data from other regions, such as the North Atlantic where this proxy has most successfully been applied, requires careful consideration of regional oceanography and knowledge of the composition of the water masses being investigated.  相似文献   

17.
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   

18.
Total dissolved chromium concentrations have been determined for four vertical profiles from Baffin Bay, the Labrador Sea and the northwest Atlantic Ocean. Chromium concentrations of 3.3 to 5.2 nM are found. While the vertical distribution of chromium in the study area is largely controlled by advective processes, the profiles show a small depletion in surface water with increase to a more constant level at depth. Surface depletion and correlations between chromium and nutrients indicate biogeochemical cycling of chromium. At one station, close to the Gibbs fracture zone, a distinct chromium maximum is observed. This feature centred at 3200 m is deeper than the core of the ambient water mass which is advected westward from the Eastern Basin of the Atlantic Ocean through the Gibbs fracture zone.  相似文献   

19.
Very high concentrations of copper lead, zinc, and to a lesser extent mercury, are present in the estuary of the Rio Tinto in South-West Spain. At the mouth of the estuary, the concentrations of these metals fall very sharply towards the natural levels of these metals in organisms living in this part of the Atlantic.  相似文献   

20.
Particulates amounting to 0.1–2.0 g efficiently collected from large volumes of Atlantic and Pacific surface waters have been analyzed for carbonate, opal, quartz and several natural and man-made radioisotopes.The concentrations of particles range between 10 and 600 μg/kg. In the equatorial regions particle concentrations are low and similar in both the oceans. At higher latitudes (>30°N or S), the Atlantic waters, however, have higher concentrations of particles compared to those in the Pacific. The latitudinal distribution exhibits a north-south symmetry with higher concentrations in the 30°–60° belt. Based on the particulate abundance for CaCO3 and opal and their sedimentation, we have estimated their production and in-situ integrated dissolution rates for a few regions.Radioisotopes having different source functions, namely14C and239Pu injected due to nuclear weapon tests,234Th,230Th and228Th produced in-situ in seawater,232Th which derives primarily from land,210Pb introduced via wet precipitations and226Ra introduced through diffusion from deep-sea sediments have been measured in the particulates. The relative enrichment factors for these nuclides in particles vary as Th ? Pu > Pb > Ra. The atmospheric bomb fallout pattern is discernible in the surface particulates; the239Pu concentration increases with latitude in both the hemispheres; however, the values are about a factor of two lower in the southern hemisphere.The distribution pattern of radioisotopes is found to be complex, even for234Th whose source function in the oceans is uniform. In view of the differences in the source functions it becomes possible to delineate the principal geochemical/geophysical processes which determine the concentrations of these nuclides in surface waters.  相似文献   

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