Lead in the southern East China Sea

At present, in most oceans the lead (Pb) biogeochemical cycling has been disturbed by anthropogenic Pb through atmospheric input. The Pb concentrations in the upper water positively correlate with atmospheric input fluxes of Pb. The North Pacific is affected greatly by atmospheric substances via long-range transport from eastern Asia, especially from Mainland China. Mainland China may export considerable amounts of pollutants into the seas via rivers and the atmosphere owing to its recent fast growth in industry and economy. The East China Sea lies in an important geographical position--a transit between Mainland China and the western North Pacific. However, no data are available for seawater concentrations of Pb, a representative element with anthropogenic origin. In this work seawater samples from both 5 and 30-50 m water layers of 15 stations occupied over a cyclonic eddy in the southern East China Sea were analyzed for particulate Pb (PPb) and dissolved Pb (DPb). The Mean concentration of DPb (approximately 128 ng/l) in the southern East China Sea upper waters (< or = 50 m) is approximately several times higher than those in the Pacific; the high DPb concentrations in the southern East China Sea waters correspond to much higher atmospheric supplies of Pb to the East China Sea. Thus, this study partly fills the 'data gap' of the marginal seas. Also, it indicates that the East China Sea may be considerably contaminated by deposited polluted aerosols. Spatial distributions of DPb in the surface water show a tendency of increasing concentrations with distance offshore, that depends on the magnitudes of atmospheric Pb inputs and on particle scavenging processes. In contrast to DPb, spatial distributions of PPb basically display an 'omega'-like picture and a tendency of decreasing concentrations with distance offshore. These are related to riverine and scavenging sources and to the drive by the eddy. Additionally, the residence times of DPb in the surface water were estimated to be about 2 years, agreeing well with the reported data.     

Chemical fractionation of zinc versus cadmium among other metals nickel, copper and lead in the northern North Sea

Concentrations of dissolved Ni, Cu, Zn, Cd and Pb were measured in water samples collected during a cruise with R.V Pelagia (29-6/14-7-1993) in the northern North Sea and N.E. Atlantic Ocean. At least six depths (0–90 m) were sampled with modified Go-Flo samplers from a rubber zodiac. In the study area, the first 25 m were well mixed and stratification occurred below this depth. The local bloom of Emiliania huxleyi hardly affected the trace metals concentration, except for some removal of Cd as seen from its correlation with nitrate. The mean dissolved concentrations were for Ni (3.66 nM), Cu (1.61 nM), Zn (4.5 nM), Cd (48 pM) and Pb (108 pM). These concentrations are among the lowest reported for the North Sea and are of similar magnitude to those found in the eastern North Atlantic at the same latitude. Zn was the only exception with values 10 times higher compared to those in the Atlantic Ocean, suggesting external inputs, mainly atmospheric and possibly from surrounding land masses. The observed ratio Zn:Cd in the North Sea and estuaries is in between the high ratio 600–900 for continental sources and the low ratio 5–10 for oceanic waters. Latter low ratio is consistent with the 21-fold stronger inorganic complexation of Cd in seawater which, in combination with the preferential biological uptake of Zn, may lead to the observed about hundredfold fractionation of Zn versus Cd in the marine system. Other processes may play a role but would need further investigation. The dissolved Pb values tend to be lower than found before in the North Sea, indicating decreasing inventories due to reduced anthropogenic emissions.     

Metal distributions and their fluxes at the coastal boundary of a semi-enclosed ria

Water column samples have been collected in the outer channel of the Ferrol Ria (NW Spain) during four occasions over a tidal cycle. The objective was to study the exchange of dissolved and particulate Cd, Cu, Pb and Zn and particulate Al, Fe and Si between the ria and the adjacent coastal waters. This study provides the first extensive dataset on dissolved and particulate metal concentrations in the water column of a Galician ria. Typical concentrations of dissolved Cd (96 ± 31 pM), Cu (8 ± 4 nM), Pb (270 ± 170 pM) and Zn (21 ± 10 nM) were similar than in other European Atlantic shelf and coastal waters. The fraction of metals in the particulate phase followed the trend: Pb > Cu Zn > Cd. The outgoing water from the ria was enriched in dissolved and particulate Cu, Pb and Zn compared with incoming waters, whereas Cd concentrations were similar for both waters. The suspended particulate matter was composed of a mixture of marine and continental material. The latter end-member was found to arise from the metal-rich ria bed sediments, which is diluted by the dominant metal-poor marine end-member. The net output flux of Cu from the channel is balanced by the freshwater inputs to the ria, and the net Zn flux gave a positive output to coastal waters. For Pb, the net flux to the coastal waters is less than that input from the rivers, as a result of its particle reactivity and deposition in sediments. On the contrary, a net input flux of dissolved Cd from coastal waters was observed, highlighting the oceanic source of this metal in the Galician rias. Results from the budget calculations are in agreement with the differential geochemical behavior of these elements in coastal waters.     

Trace metal (Cd,Cu, Ni and Pb) cycling in the upper water column near the shelf edge of the European continental margin (Celtic Sea)

This study investigates the relative importance of processes that affect trace metal (TM) cycling in the upper water column at the shelf edge of the Celtic Sea on the western European continental margin. The examined processes include external inputs (by atmosphere and river), physical factors (upwelling, winter mixing and water mass advection) and biological processes (in situ uptake, regeneration and export to deep waters). The concentrations of dissolved Cd, Cu, Ni and Pb were measured with this aim in January 1994 and June 1995 at vertical stations across slope, including stations with upwelling, and in the surface waters along the Celtic Sea shelf. Additionally, deep sea (from sediment trap data) and atmospheric fluxes were estimated. The metal profiles over the slope off the Celtic Sea are quite similar to open ocean profiles already described in the northeast Atlantic, and the concentrations in surface waters are only slightly enriched compared to the nearby open ocean (1.2–1.3× for Cd and Ni). The external sources to the system appear to be of weak influence: the fluvial input is locally strong at the coast and then “diluted” along the large continental shelf; the atmospheric deposition is not significant at the annual scale in comparison to the metal content in the upper waters of the shelf edge (at least for Cd, Ni and Cu). In the upwelling zone, a significant increase in concentrations was observed in the summer surface mixed layer (×2 for nitrate and Cd and ×1.5 for Ni) in comparison to the non-upwelling zone. In winter, concentrations of bioreactive metals increased significantly in the surface waters in comparison to the low summer levels (×5 for nitrate and Cd). Our results suggest that upwelling and winter mixing act as regenerated sources that lead to the resupply of the bioreactive elements above the permanent thermocline with a low export to deeper waters. The tracing of the Mediterranean intermediate waters (MIW) from Gibraltar to the studied area shows indeed that its elemental content at the Celtic shelf edge is mainly due to the conservative mixing of the three “end-member” component waters which are thought to make up the MIW. The remineralization of organic matter within this water mass during its transport to the north would contribute only 20% of the nutrients and Cd concentrations recorded at the Celtic Sea shelf edge. According to the correlation found with nutrients in the 10–200-m layer, dissolved Pb would also be subjected to biological uptake and regeneration within the seasonal thermocline. Particulate scavenging removal of Pb would take place below the permanent thermocline throughout the water column.     

Behaviors of dissolved and particulate Co,Ni, Cu,Zn, Cd and Pb during a mesoscale Fe-enrichment experiment (SEEDS II) in the western North Pacific

During mesoscale Fe enrichment (SEEDS II) in the western North Pacific ocean, we investigated dissolved and particulate Co, Ni, Cu, Zn, Cd and Pb in seawater from both field observation and shipboard bottle incubation of a natural phytoplankton assemblage with Fe addition. Before the Fe enrichment, strong correlations between dissolved trace metals (Ni, Zn and Cd) and PO₄³⁻, and between particulate trace metals (Ni, Zn and Cd) and chlorophyll-a were obtained, suggesting that biogeochemical cycles mainly control the distributions of Ni, Zn and Cd in the study area. Average concentrations of dissolved Co, Ni, Cu, Zn, Cd and Pb in the surface mixed layer (0–20 m) were 70 pM, 4.9, 2.1, 1.6, 0.48 nM and 52 pM, respectively, and those for the particulate species were 1.7 pM, 0.052, 0.094, 0.46, 0.037 nM and 5.2 pM, respectively. After Fe enrichment, chlorophyll-a increased 3 fold (up to 3 μg L⁻¹) during developing phases of the bloom (<12 days). Mesozooplankton biomass also increased. Particulate Co, Ni, Cu and Cd inside the patch hinted at an increase in the concentrations, but there were no analytically significant differences between concentrations inside and outside the patch. The bottle incubation with Fe addition (1 nM) showed an increase in chlorophyll-a (8.9 μg L⁻¹) and raised the particulate fraction up to 3–45% for all the metals, accompanying changes in Si/P, Zn/P and Cd/P. These results suggest that Fe addition lead to changes in biogeochemical cycling of trace metals. The comparison between the mesoscale Fe enrichment and the bottle incubation experiment suggests that although Fe was a limiting factor for the growth of phytoplankton, the enhanced biomass of mesozooplankton also limited the growth of phytoplankton and the transformation of trace metal speciation during the mesoscale Fe enrichment. Sediment trap data and the elemental ratios taken up by phytoplankton suggest that export loss was another reason that no detectable change in the concentrations of particulate trace metals was observed during the mesoscale Fe enrichment.     

THE CONCENTRATION AND DISTRIBUTION OF TRACE METALS IN THE SURFACE WATERS OF XIAMEN HARBOR

Dissolved, weakly and strongly bound particulates Cu, Pb, Zn, Cd, Co, Ni and Fe have been measured in the surface water sampled from eleven stations in Xiamen Harbor by clean laboratory methods and GFAAS. The average concentrations found in dissolved fractions are Cu: 0.41±0.12; Pb: 0.014±0.008; Zn: 0.084±0.043; Cd: 0.022±0.004; Co: 0.009±0.004; Ni: 0.15±0.02; and Fe: 0.15± 0.02 μg/kg, which make up 62%, 6%, 12%, 85%, 5%, 25% and <1% of the total metals in the surface water respectively. The results are mucn lower than those reported previously in the coastal waters of China. Industrial sources of trace metal contamination are likely responsible for the distribution of trace metals.     

Sources of Cd, Cu, Ni and Zn in Portuguese coastal waters

In order to identify the major sources of trace metals (TM) in the Portuguese coastal waters, 58 surface water samples were collected during September 1988. The area sampled extended from the Tagus Estuary (down to a salinity of 25) to cape Ste Marie on the southern coast of Portugal. Dissolved metal concentrations in the fully marine waters ranged from 30 to 250 pM for Cd, 0.7–15 nM for Cu, 0.9–20 nM for Zn and 1.8–4.5 nM for Ni. Within the Tagus Estuary (salinity 25), concentrations increased to 3400 pM for Cd, 26 nM for Cu, 14 nM for Ni and 230 nM for Zn.The large-scale distribution of these metals is dominated by two strong continental sources, both probably linked to the exploitation of pyrite ores. In the Tagus Estuary, TM enrichments can be mostly attributed to a pyrite roasting plant located on the shore in front of Lisbon. Concerning the south Portuguese shelf waters, several hypotheses are proposed to explain their elevated metal concentrations. We particularly discussed the likely influence of the Tinto/Odiel rivers located 100 km eastward, an influence well known in the shelf waters of the Gulf of Cadiz. These rivers are extremely metal-rich because of acid mine tailings originating from their catchment. Between these two regions, upwelling of relatively metal-poor water largely contributes to the dilution of the continental inputs. Indeed, water exchanges on the shelf linked to the upwelling involve water fluxes 500 times higher than the Tagus River flow, and renew the coastal waters that are thus cleaned from terrestrial contamination. Contrary to many other upwelling systems in non-contaminated areas, the Portuguese upwelling does not act as a source of trace-metal enrichment of the continental margin waters.     

Concentration and Regeneration of Cd in the Japan Sea Proper Water

The concentration level of cadmium (Cd) and the regeneration related to phosphate (PO₄) were examined at two stations (CM10, CM12) in the eastern Japan Basin in July 1998. The observed Cd concentrations were around 0.2–0.3 nM and 0.5–0.6 nM in the surface and deep layers (Japan Sea Proper Water; JSPW), respectively; the concentration of Cd in the JSPW was much lower than that in the Pacific deep water, which is attributed to its specific formation system (which driven by the winter convection of the surface layer within the Japan Sea, thereafter descending to the deep layer) connected with the relatively active vertical mixing in the Japan Sea. A plot of Cd against PO₄ showed good linearity with positive y-intercept values, suggesting that the excess Cd was apparently not available in the biogeochemical cycle. The molecular ratios of consumed O₂ to regenerated Cd and PO₄ in the JSPW were 688,000, 140 and 881,000, 146 for CM10 and CM12, respectively, and a lower preformed Cd concentration (around 0.37 nM) was also estimated in the JSPW, different from that of the North Pacific deep water (613,000 for Cd, 170 for PO₄, and 0.64 nM of preformed Cd).     

Cadmium, copper and nickel distributions at four stations in the eastern central and south Atlantic

Distributions of cadmium, copper and nickel at four stations in the eastern part of the Atlantic Ocean from 30 ° S to 34 ° N are described based on analytical results from three laboratories. The Cd and Ni profiles show nutrient-like distributions with concentrations in the deep waters increasing from north to south. Copper profiles all show gradual increases from surface to bottom with the highest concentrations occurring near bottom on the most northerly station.Variations in the deep-water Cd and Ni concentrations can be understood in terms of mixing of southern source waters with high concentrations with lower concentration northern source waters. The deep-water Cu distributions indicate a significant near-bottom source to the northern end of the section.Cadmium vs. phosphate relationships show features that result from both regeneration and mixing. Higher Cd:PO₄ ratios are seen in the southern source waters than in the northern waters, thus discounting the suggestion that the inflection in the global Cd:PO₄ relationship at PO₄ ≈ 1.3 μM originates in the southern ocean. Differential regeneration of Cd and PO₄ is seen through the equatorial oxygen minimum.     

Dissolved Cu, Pb, Zn and Cd in the South China Sea surface waters

The understanding of the distribution of trace heavy metals in the world ocean has greatlyimProved in the past decades. But most of the data are of vertical profiles of certain stations(Bruland, l980; Paul et al., l992; RObert et al., l990) and large--scale study of temporaland spatial variability of trace heaVy metals in the ocean is rather few. In fact, affected by ver-tical mixing by upwelling or convection, biogenic removal, atmospheric fallout and continentalinput frorn rivers, the dist…     

南海表层水中的溶解态Cu,Pb, Zn,Cd

于1998年“南海海洋环境调查”外业工作期间在南海的各个站位,按照严格的防沾污措施采集了106个表层海水样品.采用溶剂萃取-石墨炉原子吸收法对样品中的痕量重金属Cu,Pb,Zn,Cd含量进行了分析测试.测得各重金属的平均值如下:Cu 0.100 μg/dm3,Pb 0.060μg/dm3,Zn 0.086 μg/dm3,Cd 0.007μg/dm3,接近世界大洋水的浓度水平.各重金属的空间分布呈现出海区周边含量高于中央,浓度有自近岸向远海逐渐减小的趋势.相关分析的结果表明各重金属夏季相关性优于冬季,Cu与Cd存在良好的正相关关系,并且首次在南海表层水发现Cu,Cd与营养盐的相关关系.将重金属浓度值作数理统计分析,得到它们在南海的基线值.     

Trace element distributions in coastal waters along the US-Mexican boundary: relative contributions of natural processes vs. anthropogenic inputs

Trace element concentrations (Pb, Cd, Mn, Fe, and Zn) were measured along four surface water transects across the continental shelf off Baja California, to evaluate the magnitude of heavy metal contamination in the coastal waters along the US-Mexican boundary. These initial measurements of trace elements in Mexican neritic waters revealed offshore concentration gradients, with the highest levels in coastal waters with high salinities and nutrient concentrations. There were also longshore gradients, with lower concentrations in the southern locations. Although the relative enrichment of metals detected at nearshore stations along the US-Mexican border appeared to correspond to wastewater discharges in that area, these trace metal enhancements were found to be primarily associated with physical oceanographic processes (upwelling and advection), rather than anthropogenic inputs. This was demonstrated both by metal-nutrient correlations and multivariate statistical analyses. Mass balance calculations also indicated that about 1% of Cd, 9% of Zn, and 29% of Pb were from urban discharges within the area.     

Cadmium and phosphate in coastal Antarctic seawater: Implications for Southern Ocean nutrient cycling

Cadmium is a biologically important trace metal that co-varies with phosphate (PO₄³⁻ or Dissolved Inorganic Phosphate, DIP) in seawater. However, the exact nature of Cd uptake mechanisms and the relationship with phosphate and other nutrients in global oceans remain elusive. Here, we present a time series study of Cd and PO₄³⁻ from coastal Antarctic seawater, showing that Cd co-varies with macronutrients during times of high biological activity even under nutrient and trace metal replete conditions. Our data imply that Cd/PO₄³⁻ in coastal surface Antarctic seawater is higher than open ocean areas. Furthermore, the sinking of some proportion of this high Cd/PO₄³⁻ water into Antarctic Bottom Water, followed by mixing into Circumpolar Deep Water, impacts Southern Ocean preformed nutrient and trace metal composition. A simple model of endmember water mass mixing with a particle fractionation of Cd/P (α_Cd–P) determined by the local environment can be used to account for the Cd/PO₄³⁻ relationship in different parts of the ocean. The high Cd/PO₄³⁻ of the coastal water is a consequence of two factors: the high input from terrestrial and continental shelf sediments and changes in biological fractionation with respect to P during uptake of Cd in regions of high Fe and Zn. This implies that the Cd/PO₄³⁻ ratio of the Southern Ocean will vary on glacial–interglacial timescales as the proportion of deep water originating on the continental shelves of the Weddell Sea is reduced during glaciations because the ice shelf is pinned at the edge of the continental shelf. There could also be variations in biological fractionation of Cd/P in the surface waters of the Southern Ocean on these timescales as a result of changes in atmospheric inputs of trace metals. Further variations in the relationship between Cd and PO₄³⁻ in seawater arise from changes in population structure and community requirements for macro- and micronutrients.     

The behaviour of dissolved Cd, Co, Zn, and Pb in North Atlantic near-surface waters (30°N/60°W–60°N/2°W)

In September 1993 (M26) and June/July 1996 (M36), a total of 239 surface samples (7 m depth) were collected on two transects across the open Atlantic Ocean (224 samples) and northwest European shelf edge area. We present an overview of the horizontal variability of dissolved Cd, Co, Zn, and Pb in between the northwest and northeast Atlantic Ocean in relation to salinity and the nutrients. Our data show a preferential incorporation of Cd relative to P in the particulate material of the surface ocean when related to previously published parallel measurements on suspended particulate matter from the same cruise. There is a good agreement with results recently estimated from a model by Elderfield and Rickaby (Nature 405 (2000) 305), who predict for the North Atlantic Ocean a best fit for α_Cd/P=[Cd/P]_POM/[Cd/P]_SW of 2.5, whereas the approach of our transect shows a α_Cd/P value of 2.6. The Co concentrations of our transects varied from <5 to 131 pmol kg⁻¹, with the lowest values in the subtropical gyre. There were pronounced elevations in the low-salinity ranges of the northwest Atlantic and towards the European shelf. The Co data are decoupled from the Mn distribution and support the hypothesis of marginal inputs as the dominant source. Zinc varied from a minimum of <0.07 nmol kg⁻¹ to a maximum of 1.2 and 4.8 nmol kg⁻¹ in regions influenced by Labrador shelf or European coastal waters, respectively. In subtropical and northeast Atlantic waters, the average Zn concentration was 0.16 nmol kg⁻¹. Zinc concentrations at nearly three quarters of the stations between 40°N and 60°N were <0.1 nmol kg⁻¹. This suggests that biological factors control Zn concentrations in large areas of the North Atlantic surface waters. The Pb data indicated that significant differences in concentration between the northwest and northeast Atlantic surface waters presently (1996) do not exist for this metal. The transects in 1993 and 1996 exhibited Pb concentrations in the northeast Atlantic surface waters of 30 to 40 pmol kg⁻¹, about a fifth to a quarter of the concentrations observed in 1981. This decline is supported by our particle flux measurements in deep waters of the same region.     

Natural and anthropogenic sources of Hg,Cd, Pb,Cu and Zn in seawater and sediment of Mljet National Park,Croatia

Distributions of Hg, Cd, Pb, Cu and Zn in seawater and sediment from Mljet National Park, Adriatic Sea are presented for the first time. Natural and anthropogenic factors play an important role in determining resultant trace metals' concentrations in the region. We place particular emphasis on the saline “lakes” of Malo Jezero and Veliko Jezero, which have restricted flows of seawater. In Malo Jezero lake, fresh karstic spring water generated by flooding, and weathering of dolomites are the main sources of naturally elevated Cd, Pb and Zn concentrations (20.7 ± 1.6, 289 ± 19, 1260 ± 0.08 ng L^?1, respectively); anthropogenic input is negligible. In Veliko Jezero lake enhanced Cu and Zn contents originate from anthropogenic input (tourism and agriculture). Distributions of the Pb and Zn in the water columns of both lakes are influenced by natural aragonite precipitation and sedimentation. Exceptionally high total Hg concentrations of 24.2 and 33.7 ng L^?1 in the water column of Malo Jezero, sampled during periods of high rainfall associated with strong eastern winds, suggest an airborne input. Total Hg concentrations in waters of both lakes are elevated because of inefficient mixing. Two different metal distribution patterns exist in the sediment columns. First, Hg, Pb, Cu and Zn show elevated concentrations in recent sediments due to anthropogenic input. Second, Cd content increases with depth due to reprecipitation via a downward redox boundary shift.Described natural processes, as well as anthropogenic influence, enhance levels of trace metals. Careful study followed by suitable interpretation based on geochemical data were necessary to distinguish natural from anthropogenic sources.     

中国黄、渤海海水中溶解镉的形态研究

黄、渤海是我国重要的海洋经济渔业开发区域,海水中痕量金属的含量及其存在形态会对海洋环境、海洋渔业产生重要影响。随着近年我国痕量金属采集与分析测试技术的发展,数据的准确性有了新的提升。2016-06—07采集黄、渤海40个站位的海水样品,测定其溶解态金属Cd的总浓度,并应用电化学方法(阳极溶出伏安法)分析Cd存在形态。结果表明,渤海海水中的总溶解态Cd浓度是南黄海海水中的2~3倍,这可能与渤海海水停留时间较长,水深较浅,周边较多河流输入有关。20%~92%以上的溶解态Cd是以有机络合物形态存在,以自由离子态存在的Cd浓度不超过100 pmol/L,低于Cd对浮游生物的毒性阈值。渤海比黄海的金属配体浓度高出2倍以上,高值出现在黄河口周围海域,表明黄河水携带较多有机配体输入。推测我国近海有机配体来源可能包括陆源输入、沉积物再悬浮的解析过程以及藻类分泌。研究还表明,黄、渤海海水中溶解态Cd的有机配体络合常数较其他海域的稍高,这与我国近海废、污水排放的有机络合配体类型有关。     

Relationship between cadmium and phosphate in the northwest Pacific Ocean

The relationship between Cd and PO₄ in the Kuroshio and Oyashio regions and the Okhotsk Sea was examined. The resultant equations are as follows: Cd (ng l^–1)=37.0 PO₄ (M)+2.6; Cd(ng l^–1)=32.1 PO₄ (M)+1.2 and Cd (ng l^–1)=34.1 PO₄ (M)+7.9, respectively. These results are in good agreement with previously reported studies, and indicate that during removal from surface waters to deeper waters by biological assimilation and regeneration in deeper waters Cd and PO₄ maintain the same ratio in the open ocean. The relationship between Cd and PO₄ in coastal waters, however, differed from that in the open ocean.     

Trace metal concentrations in the Ross Sea and their relationship with nutrients and phytoplankton growth

Dissolved and particulate trace metal concentrations (dissolved Fe, Zn, Cd, Co, Cu and Ni; particulate Fe, Mn and Al) were measured along two transects in the Ross Sea during austral summer of 1990. Total Fe concentrations in southern Ross Sea and inshore waters were elevated >3.5 times that of northern waters. Dissolved Zn, Cd and Co concentrations were lower by factors of 4.5, 3.5 and 1.6 in southern surface waters relative to northern waters. Dissolved Cu and Ni concentrations were similar in both areas. Elevated Fe concentrations coincided with areas of increased productivity, phytoplankton biomass and nutrient drawdown, indicating that Fe is an important factor controlling the location of phytoplankton blooms in the Ross Sea. Particulate concentrations of Fe, Mn and Al indicate two possible sources of iron to the Ross Sea, resuspension of continental shelf sediments and iron incorporated in annual sea ice and released with meltwaters.     

Metals background and enrichment in the Chiloé Interior Sea sediments (Chile). Is there any segregation between fjords,channels and sounds?

The range and spatial distribution of metal concentrations in the Chiloé Interior Sea were investigated from 37 surface sediment samples collected during the ‘CIMAR 10 Fiordos’ cruise. Grain size distribution, total organic carbon and nitrogen, δ¹³C, major (Al, Fe, and biogenic opal) and trace (Cd, Co, Cu, Ni, Pb, and Zn) elements were determined. Metal background concentrations of each metal in sediment were defined from linear regression equations of metal versus Al, as baseline information for future research on the status of sediment contamination in the Northern Patagonian marine area. Metal levels in Chiloé sediments were of the same order of magnitude as uncontaminated sediments around the world and contamination can be considered negligible-moderate (normalized enrichment factors lower than 3) in this Southern Pacific Region. The Chiloé Interior Sea can be segregated into two zones on the basis of metal content by applying a principal component analysis. The first pertains to inner fjords and it has terrestrial origin (associated to Co, Cu, Pb, Zn) and the second zone features channels and gulfs of a predominantly marine source (Cd, Cu). Nevertheless, only one background equation is needed to predict metal concentrations in the natural sediment of the Chiloé Interior Sea.     

Outflow of trace metals into the Laptev Sea by the Lena River

Freshwater concentrations confirm the pristine character of the Lena River environment as already pointed-out in a previous study with a limited set of data (Martin et al., 1993). Total dissolved concentrations of the freshwater are 13.8 ± 1.6 nM, Cu, 4.4 ± 0.1 nM, Ni, 0.054 ± 0.047 nM, Cd, 642 ± 208 nM, Fe, 0.2–0.3 nM Pb and 1.2 ± 1.0 nM, Zn. For Zn and Pb, a simple mixing of the Lena River waters with the Arctic waters is observed. Relationships with salinity suggest that for Cu, Ni and Cd, there is a mobilization of the dissolved fraction from the suspended matter, with an increase of the dissolved concentration of 1.5, 3 and 6 times, respectively. For Fe, the total dissolved concentrations follow an exponential decrease in the mixing zone and 80% of the total “dissolved” Fe is removed from the solution. For Cu, Ni, Cd and Fe, the riverine end-members are 20 nM, 12 nM, 0.3 nM and 47 nM, respectively. When considering the input of total dissolved metals to the Arctic Ocean, the fraction attributed to the freshwaters from the Arctic rivers appears to be small (4% of the input of dissolved metal to the Arctic Ocean for Cd, 27% for Cu, 11 % for Ni and 2% for Zn). Metal concentrations in the Laptev Sea and Arctic Ocean are very similar, indicating a generally homogeneous distribution in the areas sampled.