Trace metals (Cd,Cu, Ni,and Zn) and nutrients in coastal waters adjacent to San Francisco Bay,California

Samples collected in December 1990 and July 1991 show that dissolved Cd, Cu, Ni, and Zn distributions in the Gulf of the Farallones are dominated by mixing of two end-members: (1) metal-enriched San Francisco Bay water and (2) offshore California Current water. The range of dissolved metal concentrations observed is 0.2–0.9 nmol kg^?1 for Cd, 1–20 nmol kg^?1 for Cu, 4–16 nmol kg^?1 for Ni, and 0.2–20 nmol kg^?1 for Zn. Effective concentrations in fresh water discharged into San Francisco Bay during 1990–1991 (estimated by extrapolation to zero salinity) are 740–860 μmol kg^?1 for silicate, 21–44 μmol kg^?1 for phosphate, 10–15 nmol kg^?1 for Cd, 210–450 nmol kg^?1 for Cu, 210–270 nmol kg^?1 for Ni, and 190–390 nmol kg^?1 for Zn. Comparison with effective trace metal and nutrient concentrations for freshwater discharge reported by Flegal et al. (1991) shows that input of these constituents to the northern reaches of San Francisco Bay accounts for only a fraction of the input to Gulf of the Farallones from the estuary system as a whole. The nutrient and trace metal composition of shelf water outside a 30-km radius from the mouth of the estuary closely resembles that of California Current water further offshore. In contrast to coastal waters elsewhere, there is little evidence of Cd, Cu, Ni, and Zn input by sediment diagenesis in continental shelf waters of California.     

10 Be在大洋边缘海洋学中的应用及模型

主要讨论宇宙射线成因核素¹⁰Be（T _1/2＝ 1．5Ma）在大洋边缘海洋学尤其是中国近海海洋研究中的应用。在过去的近20年中，在中国开展的¹⁰Be研究在黄土堆积年龄及地层对比方面获得了诸多成果，但在海洋方面的应用研究距国际水平仍有一定的差距，尚需进一步加强。综述了海洋环境中¹⁰Be作为一个地球化学示踪剂的研究现状，着重介绍¹⁰Be在中国东部海域的收支平衡模式以及讨论¹⁰Be在太平洋西部边缘海及岛弧地区的应用前景。     

Transport of dissolved organic nitrogen in Mississippi River plume and Texas-Louisiana continental shelf near-surface waters

Dissolved organic nitrogen (DON) in near-surface (<20 m depth) waters of the Texas-Louisiana continental shelf is the predominant form of total dissolved nitrogen that is advected by the Mississippi-Atchafalaya River plume. Relatively high DON concentrations associated with low-salinity (<33 psu) waters throughout the year can be traced within the plume along the Texas-Louisiana inner shelf. DON concentrations throughout the shelf were significantly higher near the Mississippi-Atchafalaya outflow region relative to downstream inner Gulf shelf locations. Significant intercruise variations were also evident, with the highest concentrations during May 1992 and lower values in October 1992. At a fixed location off the Mississippi River outflow region DON concentration covaried inversely with salinity on time scales of hours to months, confirming that source water is a determining factor for variations of bulk DON concentrations in the region. Similar variations in upper water DON concentrations at different locations and seasons occurred in both plume and nonplume waters, which resembled the seasonal concentration changes of riverine nitrogen, and show that this pool is useful in tracing the influence of riverine-derived nitrogen on the overall nitrogen balance of the NW Gulf of Mexico’s continental shelf. Plume and nonplume DON concentrations deviated from mixing lines between riverine and oceanic endmembers, suggesting that plume waters may be a sink and nonplume waters may be a source of a labile fraction of DON in the region.     

Depositional controls on Palaeoproterozoic iron formation accumulation, Gogebic Range, Lake Superior region, USA

Shallowing‐upward, decametre‐scale, Palaeoproterozoic iron formation cycles in northern Wisconsin record the combined effects of tectonism and changing oceanographic conditions on a storm‐dominated shelf. Cycles consist of a lower unit of laminated, Fe‐ and Si‐rich chemical mudstone that is transitional into an upper unit dominated by trough cross‐stratified chert grainstone. Grainstone lenses become progressively thicker upwards in cycles with the largest at cycle tops, where they are sharply overlain by a unit of slumped chemical mudstone. The cycles developed through progradation when offshore‐directed storm currents transported chert sand intraclasts that were formed in nearshore settings into middle and distal shelf environments. Abrupt subsidence events, probably resulting from normal faulting associated with extensional tectonism, repeatedly terminated chert grainstone accumulation and may also have generated the slumped units at cycle boundaries. The episodic storm currents are also interpreted to have transported biologically oxygenated waters from the shallow‐water, inner shelf into otherwise anoxic bottom waters of the strongly stratified distal shelf. The consequence of such transport and mixing was rapid deposition of chemical mud, mainly as precipitated Fe‐oxide. In many cases, the resultant decrease in Fe²⁺ in the water column, together with pelagic inorganic precipitation of SiO₂ and rainout of terrigenous clays, resulted in submillimetre‐ to millimetre‐thick, chemically graded laminae. The concomitant decreasing Fe²⁺/Mn²⁺ ratio also led to increasing Mn‐compound precipitation and enrichment in the upper portions of some chemically graded layers.     

The marine chemistry of iodine in anoxic basins

The distribution of dissolved iodate and iodide has been determined in two anoxic basins, the Black Sea and the Cariaco Trench; and the oxic Venezuela Basin which serves as a comparison for normal oceanic conditions. In normal oceanic waters, iodate is the predominant species; its concentration is lowest at the surface (ca. 0.3 μM) and increases with depth to ca. 0.5 μM. In contrast, the iodide concentration shows maximum values in surface waters and rapidly decreases to <0.01 μM below the euphotic zone. In anoxic basins, the reduced pE reverses this trend. The concentration of iodide increases rapidly in the oxygen-sulfide mixing zone from 0.02 to 0.46 μM, and 0.01 to 0.43 μM, in the Cariaco Trench and the Black Sea, respectively. The iodate concentration, meanwhile, decreases to zero.The total iodine to salinity ratio is lower in the surface waters with a range of 7.3–12.1 nmoles/g suggesting a possible depletion by organisms. In the anoxic basins, a maximum in this ratio is observed just above the oxygen-sulfide boundary (15–17 nmoles/g) and is indicative of particle dissolution in a strong pycnocline. In the anoxic zone of the Cariaco Trench, the ratio is constant at 12.3 nmoles/g, whereas in the Black Sea, it increases with depth from 10.0 to 19.3 nmoles/g, suggesting a possible flux of iodide from the bottom sediments.By considering the distribution of iodate and iodide in oxic and anoxic basins, the lower limit of the pE of the oxic ocean is estimated to be 10.7, given our present analytical capability. Thermodynamic considerations further suggest that the iodide-iodate couple is a poor indicator for the pE of the oceans with a limited usable range of 10.0–10.7.     

Nitrogen flow and the interaction of Boston harbor with Massachusetts Bay

This paper summarizes evidence that most of the considerable nitrogen loading (～8, 470 mmol total N m^?2 yr^?1) to Boston Harbor (Massachusetts, USA) is expelled to shallow shelf waters of Massachusetts Bay, where it strongly influences ecological dynamics. Examination of nitrogen concentrations in the harbor, compared with loading, indicated that removal processes are active in the harbor. Comparison to other estuarine systems showed that the harbor’s nitrogen concentrations are consistent with its loading, if they are corrected for tidal flushing effects on the water residence time. Furthermore, extensive measurements of sediment denitrification confirmed that rates of N₂ gas loss are high in an absolute sense (～600–800 mmol N m^?2 yr^?1) but nonetheless remove only a small portion (<10%) of the annual land-derived nitrogen loading. Burial in sediments apparently removes only about 2% of the N input, implying export to offshore environments as the major removal process (～88–90% of N input). Western Massachusetts Bay receiving waters were examined for a signature of export from the harbor. Data consistently show a gradient of decreasing nitrogen concentrations from the harbor to about 10–20 km into the bay. In many cases, plots of nitrogen concentrations versus salinity show nearly conservative mixing character, which implies virtual export. Seasonally, the data suggest most of the export from the harbor in winter is as dissolved inorganic forms (NH₄ ⁺, NO₃ ^?, NO₂ ^?). In summer, export is dominated by the outflow of organic nitrogen forms. Chlorophyll export is evident as well, suggesting that the nutritional coupling of the harbor and bay in summer involves organic fertilization of the bay’s surface water. Finally, high-resolution studies over different stages of the tidal cycle help refine understanding of the advection of chlorophyll and stimulation of in situ chlorophyll growth at the seaward edge of the tidal excursion into the bay.     

The contrasting biogeochemistry of iron and manganese in the Pacific Ocean

Vertical and horizontal distributions of dissolved and suspended particulate Fe and Mn, and vertical fluxes of these metals (obtained with sediment traps) were determined throughout the Pacific Ocean. In general, dissolved Fe is low in surface and deep waters (0.1 to 0.7 nmol/kg), with maxima associated with the intermediate depth oxygen minimum zone (2.0 to 6.6 nmol/kg). Vertical distributions of dissolved Mn are similar to previous reports, exhibiting a surface maximum, a subsurface minimum, a Mn maximum layer coincident with the oxygen minimum zone, and lowest values in deep waters.Near-shore removal processes are more intense for dissolved Fe than for dissolved Mn. Dissolved Mn in the surface mixed layer remains elevated much farther offshore than dissolved Fe. Elevated near-surface dissolved Mn concentrations occur in the North Pacific Equatorial Current, suggesting transport from the eastern boundary. Near-surface mixed-layer dissolved Mn concentrations are higher in the North Pacific gyre reflecting enhanced northern hemisphere aeolian sources.Residence time estimates for the settling of refractory paniculate Fe and Mn from the upper water column are 62–220 days (Fe), and 105–235 days (Mn). In contrast, residence times for the scavenging of dissolved Fe and Mn are 2–13 years (Fe) and 3–74 years (Mn). Scavenging residence times for dissolved Mn based on horizontal mixing in the surface mixed layer of the northeast Pacific are 0.4 years (nearshore) to 19 years (1000 km offshore).There is no evidence for in situ Fe redox dissolution within sub-oxic waters in the eastern tropical North Pacific. Dissolved Fe appeared to be controlled by dissolution from sub-oxic sediments, with oxidative scavenging in the water column or upper sediment layers. However, in situ Mn dissolution within the oxygen minimum zone was evident.     

南印度洋海区营养盐的分布特征

探讨了南印度洋海区总有机磷(TOP)、总有机氮(TON)以及溶解无机营养盐的分布规律。分析结果表明：研究海区内溶解无机营养盐受水体中生物活动和物理过程的综合影响,表层水体由于生物活动的消耗,其磷酸盐等无机营养元素的含量一般是采样水深范围内最低的;中深层水体由于生物活动的降低以及有机质矿化作用的影响,无机营养元素的变化范围较小。表层水体中TOP和TON含量占TP和TN的主要部分,说明表层水体中的氮和磷主要以有机态形式存在,且沿着37.8°S从西向东,TOP和TON的含量以及TOP/TP和TON/TN的比值呈降低的趋势。研究海区叶绿素a的分析结果表明,初级生产力的变化可能是控制研究海区TON和TOP空间分布的主要因素。不同形态氮、磷营养元素的相关分析表明,有机营养盐和无机营养盐之间互为补充,且表层水体中有机氮和磷是水体初级生产所需营养盐的重要来源,总氮、总磷的关系表明研究区初级生产力并不受氮、磷的限制。     

湘中下石炭统粘土矿物组合特征

湖南中部下石炭统是一套以碳酸盐岩为主夹碎屑岩含煤岩系的沉积,根据粘土矿物在下石岩统剖面分布规律,结合各组段岩性岩相特征,可推断出粘土矿物组合特征及其环境分布,从滨岸碎屑沉积到滨外泥质陆棚、滨外浅水碳酸盐陆棚,到深水碳酸盐陆棚和浅海盆地,即从滨岸向盆地方向,高岭石含量急剧减少,伊利石逐渐增加,伊利石/蒙脱石混层矿物和绿泥石则先是增加,然后又趋于减少,其最高含量分别在浅水碳酸盐陆棚和滨外泥质陆棚。测水组含煤岩系粘土矿物以高岭石为主,伊利石次之,并有一定量的绿泥石和伊利石/蒙脱石混层矿物,它们在垂向上的变化反映了沉积环境水介质酸碱度和盐度的变化规律。     

Speciation Analysis for Iodine in Groundwater Using High Performance Liquid Chromatography-Inductively Coupled Plasma-Mass Spectrometry (HPLC-ICP-MS)

Methods based on high performance liquid chromatography coupled with inductively coupled plasma-mass spectrometry (HPLC-ICP-MS) for iodine speciation analysis are described. Experiments were performed relating to iodine species, preservative medium and time. The concentration and pH of the buffer are also discussed in relation to separation efficiency. The developed methods allowed the fast and sensitive determination of iodine species with detection limits of 0.025 μg l⁻¹ (as 1) for both iodide and iodate with < 5% relative standard deviation (RSD) for 50 nmol l⁻¹. Attempts were made to quantify total organo-iodine by size-exclusion chromatography (SEC). By way of example, a number of groundwater samples were analysed by these methods, revealing that iodide is the main iodine species in the sampled waters, but that high concentrations of organo-iodine compounds were observed in some samples as well. In summary, the total concentration and the dominant species of iodine in aquatic freshwater environments is easily and accurately measured using this new method.     

Development of hypoxia in well-mixed subtropical estuaries in the Southeastern USA

Esturies throughout much of the South Atlantic Bight (southeastern U.S.) have been considered to be relatively pristine, but are now experiencing elevated concentrations of both organic and inorganic nutrients. As is true in many parts of the world, this eutrophication is correlated with coastal population growth. These estuaries have been assumed to be immune from extended hypoxia, in large part because they are well mixed and do not generally exhibit the water column stratification that is traditionally associated with low concentrations of dissolved oxygen. data presented here show long-term (19 yr) decreases in dissolved oxygen in surface waters of the Skidaway estuary, a pattern that is occurring throughout coastal Georgia. More limited data from bottom waters exhibit the same trend. The decreases in dissolved oxygen occurred at the same time as observed increases in inorganic and organic nutrients and in bacteria concentrations, implying an increase in heterotrophic activity. These observations suggest that traditional paradigms long applied to stratified estuaries, wherein the cycle that leads to hypoxia is initiated by the uptake of inorganic nutrients by autotrophs that are then decomposed below the pycnocline, may need revision for well-mixed estuaries. Heterotrophic community metabolism, stimulated by anthropogenic loading of organic and inorganic nutrients, can overwhelm even vigorous vertical mixing and horizontal exchange to gradually cause declining oxygen concentrations and eventually hypoxia.     

Plutonium, 241Am and 137Cs ratios,inventories and vertical profiles in Washington and Oregon continental shelf sediments

Continental shelf sediments from nine locations off Washington and Oregon have ^239,240Pu inventories which average 8.0 ± 2.6 mCi/km². The Columbia River and seawaters advecting over the shelf supply Pu which is removed to underlying sediments, principally through scavenging by inorganic paniculate matter. Mass balance calculations argue that less than 20 percent of the advected Pu need be scavenged from the water column to balance river input and total shelf sediment inventories. The percentage of the Pu removed through scavenging is consistent with observed participate concentrations in shelf waters and published sediment/water distribution coefficients.No marked separation of Pu from ¹³⁷Cs is observed with depth in Pacific shelf sediments as has been reported in Atlantic coastal sediments. This interocean distinctness can be explained by differences in particle mixing and downward diffusion of Cs in sediments of varying porosities. The transuranic inventories and Pu/Cs ratios in the Pacific sediments do not support the hypothesis of Livingston and Bowen that Pu is remobilized within the sediment column by ‘complexone’ formation with (principally) organic substances.Excess ²¹⁰Pb/^239,240Pu inventory ratios in eight representative cores from the Washington shelf average 100 ± 19, even though absolute values of both inventories vary by much larger factors. This reasonably constant ratio, for a given water depth, permits estimation of total Pu inventories and prediction of sites of unusual Pu accumulation from data on the more easily measured natural radionuclide.     

Carbonate Chemistry Dynamics of Surface Waters in the Northern Gulf of Mexico

This paper presents the results of two cruises in the Northern Gulf of Mexico in 2008 that investigated local and short-term factors influencing the carbonate chemistry dynamics and saturation state with respect to aragonite (Ω_aragonite) of surface seawater in this region. One cruise covered much of the northern half of the Gulf, and the other focused on the coastal zone west of the Atchafalaya Bay outlet of the Mississippi River—the region where the hypoxic “dead zone” occurs on the Louisiana shelf. Offshore waters (>100 m depth) exhibited only small variations in CO₂ fugacity (fCO₂), total alkalinity (TA) and Ω_aragonite. Values were close to those typically observed in subtropical Atlantic Ocean and Caribbean Sea waters of similar salinity. However, inner shelf waters (<50 m depth) exhibited large variations in fCO₂, TA, and Ω_aragonite that were not directly related to salinity or distance from the Mississippi River plume. Changes in TA values were not the result of simple mixing of end-member freshwater and seawater TA concentrations but exhibited a minimum in values near salinity of 25. This minimum could be the result of microbial recycling across salinity gradients, biological removal of alkalinity by formation of calcium carbonate or mixing of a third end-member with a low alkalinity such as Terrebonne Bay. All waters were supersaturated with respect to aragonite. Offshore waters had an average Ω_aragonite of 3.86 with a standard deviation of only ±0.06 and inner shelf waters had a range in Ω_aragonite values from 3.9 to 9.7 with a median of 4.3. Shelf water Ω_aragonite values were elevated relative to the offshore as a consequence of both high TA input from Mississippi River and biological drawdown of CO₂. A dominant factor controlling Ω_aragonite distribution in offshore waters with relatively constant temperatures was fCO₂, with higher supersaturation occurring in areas with low fCO₂.     

Sterols in the western North Atlantic Ocean

The sterol concentrations in fourteen surface and nine deep water samples collected from the continental shelf and slope waters of the western North Atlantic and Sargasso Sea ranged from 0.1 to 1.3μ/l seawater. Isolation and structural elucidation by gas chromatography and combined gas chromatography-mass spectrometry show that cholesterol and β-sitosterol (or clionasterol) are the major free sterols in both the surface and deep water. Fucosterol, brassicasterol, 22-dehydrocholesterol, campesterol (or 22,23-dihydrobrassicasterol), 22-methylenecholesterol, norcholestadienol, and stigmasterol (or poriferasterol) are found in lower concentrations at the surface and in the deep sea. Cholesterol is the major sterol ester in both the surface and deep water, while very low concentrations of other sterol esters were found. The ratio of total free sterols to total esterified sterols is approximately two in both the surface and deep water.Marine sources of sterols in seawater include phytoplankton, yeasts, and marine animals such as Crustacea and molluscs. Terrestrial plants also may contribute. Sterol transport to the deep sea may occur by convective overturn and vertical diffusion or from vertical fluxes of large particles from the surface.     

蔬菜植物对 I–、IO–3的吸收及其生物有效性

通过水培方法培育含碘芹菜,揭示了蔬菜植物对 I–、IO–3的吸收特征,并在烹饪条件下,通过与碘盐的对比分析,研究了蔬菜植物中有机碘的生物有效性.研究结果表明,芹菜对 I–、IO–3的吸收速率随外源碘浓度的提高而增加,在不同的碘浓度下,芹菜对不同形态碘的吸收速率存在差异,这与 I–和 IO–3被吸收的方式不同有关;市售芹菜在100~160℃下爆炒90 s,添加碘盐,碘的损失率达54.80%~80.34%,含碘芹菜的碘损失率为3.00%~40.77%; 在100℃下烹煮5 min,市售芹菜加碘盐,菜和汤中的碘含量分别仅为碘添加含量的1.56%和29.03%,而含碘芹菜仍保留原始碘含量的85.26%;加醋会促使烹饪时添加的碘盐中无机碘丢失,而对含碘芹菜不产生明显影响     

Seasonal uranium distributions in the coastal waters off the Amazon and Mississippi Rivers

The chemical reactivity of uranium was investigated across estuarine gradients from two of the world’s largest river systems: the Amazon and Mississippi. Concentrations of dissolved (<0.45 μm) uranium (U) were measured in surface waters of the Amazon shelf during rising (March 1990), flood (June 1990) and low (November 1991) discharge regimes. The dissolved U content was also examined in surface waters collected across estuarine gradients of the Mississippi outflow region during April 1992, August 1993, and November (1993). All water samples were analyzed for U by isotope dilution inductively coupled plasma mass spectrometry (ICP-MS). In Amazon shelf surface waters uranium increased nonconservatively from about 0.01 μg I^?1 at the river’s mouth to over 3 μg I^?1 at the distal site, irrespective of river discharge stage. Observed large-scale U removal at salinities generally less than 15 implies a) that riverine dissolved U was extensively adsorbed by freshly-precipitated hydrous metal oxides (e.g., FeOOH, MnO₂) as a result of flocculation and aggregation, and b) that energetic resuspension and reworking of shelf sediments and fluid muds on the Amazon shelf released a chemically reactive particle/colloid to the water column which can further scavenge dissolved U across much of the estuarine gradient. In contrast, the estuarine chemistry of U is inconclusive within surface waters of the Mississippi shelf-break region. U behavior is most likely controlled less by traditional sorption and/or desorption reactions involving metal oxides or colloids than by the river’s variable discharge regime (e.g., water parcel residence time during estuarine mixing, nature of particulates, sediment storage and resuspension in, the confined lower river), and plume dispersal. Mixing of the thin freshwater lens into ambient seawater is largely defined by wind-driven rather than physical processes. As a consequence, in the Mississippi outflow region uranium predominantly displays conservative behavior; removal is evident only during anomalous river discharge regimes. ‘Products-approach’ mixing experiments conducted during the Flood of 1993 suggest the importance of small particles and/or colloids in defining a depleted U versus salinity distribution.     

Transport of particulate organic carbon by the Mississippi River and its fate in the Gulf of Mexico

This study was designed to determine the amount of particulate organic carbon (POC) introduced to the Gulf of Mexico by the Mississippi River and assess the influence of POC inputs on the development of hypoxia and burial of organic carbon on the Louisiana continental shelf. Samples of suspended sediment and supporting hydrographic data were collected from the river and >50 sites on the adjacent shelf. Suspended particles collected in the river averaged 1.8±0.3% organic carbon. Because of this uniformity, POC values (in μmol l^?1) correlated well with concentrations of total suspended matter. Net transport of total organic carbon by the Mississippi-Atchafalaya River system averaged 0.48×10¹² moles y^?1 with 66% of the total organic carbon carried as POC. Concentrations of POC decreased from as high as 600 μmol l^?1 in the river to <0.8 μmol l^?1 in offshore waters. In contrast, the organic carbon fraction of the suspended matter increased from <2% of the total mass in the river to >35% along the shelf at ≥10 km from the river mouth. River flow was a dominant factor in controlling particle and POC distributions; however, time-series data showed that tides and weather fronts can influence particle movement and POC concentrations. Values for apparent oxygen utilization (AOU) increased from ～60 μmol l^?1 to >200 μmol l^?1 along the shelf on approach to the region of chronic hypoxia. Short-term increases in AOU were related to transport of more particle-rich waters. Sediments buried on the shelf contained less organic carbon than incoming river particles. Orgamic carbon and δ¹³C values for shelf sediments indicated 3 that large amounts of both terrigenous and marine organic carbon are being decomposed in shelf waters and sediments to fuel observed hypoxia.     

Nutrient Mass Flux between Florida Bay and the Florida Keys National Marine Sanctuary

There is a net discharge of water and nutrients through Long Key Channel from Florida Bay to the Florida Keys National Marine Sanctuary (FKNMS). There has been speculation that this water and its constituents may be contributing to the loss of coral cover on the Florida Keys Reef tract over the past few decades, as well as speculation that changes in freshwater flow in the upstream Everglades ecosystem associated with the Comprehensive Everglades Restoration Plan may exacerbate this phenomenon. The results of this study indicate that although there is a net export of approximately 3,850 (±404) ton N year^?1 and 63 (±7) ton P year^?1, the concentrations of these nutrients flowing out of Florida Bay are the same as those flowing in. This implies that no significant nutrient enrichment is occurring in the waters of the FKNMS in the vicinity of Long Key Channel. Because of the effect of restricted southwestward water flow through Florida Bay by shallow banks and small islands, the volume of relatively high-nutrient water from central and eastern portions of the bay exiting through the channel is small compared to the average tidal exchange. Nutrient loading of relatively enriched bay waters is mediated by tidal exchange and mixing with more ambient concentrations of the western Florida Bay and Hawk Channel. System-wide budgets indicate that the contribution of Florida Bay waters to the inorganic nitrogen pool of the Keys coral reef is small relative to offshore inputs.     

Trace metals in sediments near offshore oil exploration and production sites in the Alaskan Arctic

Increased offshore development in the Alaskan Arctic has stimulated interest in assessing potential impacts to the environment before the onset of any adverse effects. Concentrations of trace metals in sediments are used in this paper to provide one sensitive indicator of anthropogenic inputs from offshore activity over the past several decades. Sediments in coastal waters of the western Beaufort Sea are patchy with respect to sediment granulometry, organic carbon content, and concentrations of trace metals. However, results for surface sediments and age-dated cores show that nearly all samples contain natural concentrations of Ag, Ba, Be, Co, Cr, Cu, Hg, Ni, Pb, Sb, Tl, V and Zn, with metal/Al ratios that have been constant for many decades. Metal concentrations for incoming river-suspended matter compare well with sediment metal values and, along with vertical distributions in sediments, show no discernible diagenetic impacts that distort the sedimentary record for metals, except for Mn, As and possibly Cd. Slightly elevated concentrations of Ba, Hg, Ag, Sb and Zn were observed in a total of eight instances or in only 0.7% of the 1,222 data points for metals in surface sediments.     

The geochemistry of iodine in oxidised and reduced recent marine sediments

Surface sediments from the South West Africa shelf and the Gulf of California have been analysed for iodine and organic carbon. The iodine contents range from 96 to 1990 ppm. While iodine and organic carbon show certain anomalies on the South West Africa shelf, the trend of the $\text{I}\text{C}$ ratios is smooth and decreases from the shelf edge, an area of oxidising surface sediment, shorewards to reducing sediments, formed as a result of intense water upwelling. In the Gulf of California, a similar distribution of $\text{I}\text{C}$ ratios with surface sediment type occurs; lowest values occur in the reduced sediments and highest in oxidised sediments. Values of the $\text{I}\text{C}\text{(× 10}{}^4\text{)}$ ratio of the oxidised sediments (~250) are more than an order of magnitude higher than in reduced sediments, and are similar to some other surface oxidised sediments.The high I content of oxidised sediments is mostly due to uptake of I on to plankton seston on the seabed. In reduced sediments, I contained in planktonic matter originating in surface waters forms the bulk of iodine in the sediment.With sediment burial, oxidised sediments lose most of the iodine through degradation of unspecified organic constituents. This does not happen to the same extent in reduced sediments. The geological implications of these reactions are briefly discussed.