Metal incorporation by benthic fauna: Relationships to sediment inventory

A radionuclide addition experiment was conducted in a large-scale experimental mesocosm to study the behaviour and fate of trace metals in a coastal marine environment. Twelve radionuclides (⁷Be, ¹⁰⁹Cd, ¹³⁴Cs, ⁵⁸Co, ⁶⁰Co, ⁵¹Cr, ⁵⁹Fe, ⁵⁴Mn, ²⁰³Hg, ²³³Pa, ¹¹³Sn, and ⁶⁵Zn) were added and their concentrations in benthic organisms and sediments were measured during the following nine months. The ability of benthic organisms to concentrate radionuclides was related to the vertical distribution and feeding behaviour of the organisms. Surface living fauna incorporated more radionuclides than deeper fauna. Calculations of total annual radionuclide incorporation by benthic fauna indicated that meiofauna incorporated a similar amount of the labelled metals as the macrofauna, even though the latter have a larger standing stock biomass. These calculations suggest that benthic metazoan fauna can annually cycle from 1% (Sn) to nearly 50% (Cd) of the amount of added radionuclides measured in sediments.     

大亚湾近岸沉积物对人工放射性核素的吸附

用大亚湾近岸沉积物进行人工放射性核素的吸附研究。测得各放射性核素的吸附分配系数分别为：＾８５Ｓｒ，１６０；＾１３４Ｃｓ，３３０；＾６０Ｃｏ，６４００；＾１４１Ｃｅ，９５００；＾５９Ｆｅ，９４００；＾５４Ｍｎ，１５０００。并测得核素吸附分配系数随悬浮物浓度和示踪剂活度变化的规律。当悬浮物浓度增加时，＾８５Ｓｒ，＾５９Ｆｅ的Ｋｄ值显著降低，＾１４１Ｃｅ，＾５４Ｍｎ，＾６０Ｃｏ的Ｋｄ值稍有降低，而＾１３     

Dispersion and accumulation of radionuclide in sediment of Urazoko Bay-II

Further studies on the transport in sea water and accumulation in marine sediment of the radionuclides, released from a nuclear power plant, on Urazoko Bay, Fukui Prefecture were reported.The partition of radionuclides among the particle size fractions of a sediment sample indicated that the accumulation of⁶⁰Co,¹³⁷Cs and⁵⁴Mn in the sediment were dominated substantially by the sorption on the particle surface in sea water, and the patterns of their sorption were considerably similar to each other.In regard to the⁶⁰Co contamination of marine sediments in an area of about 13 km² around the nuclear power plant, 60% of the⁶⁰Co contamination were retained in Urazoko Bay, which occupies only 7% of the bottom surface of the region.It is clear that a part of⁶⁰Co accumulated in the sediment of Urazoko Bay gradually moved to the outerward.     

大亚湾海洋沉积物的人工放射性核素

对大亚湾核电站邻近海的海洋沉积物中人工放射性核素~(144)Ce,~(103)Ru,~88Rn,~(85)Sr,~(90)Sr,~(134)Cs,~(137)Cs,~(124)Sb,~(54)Mn,~(60)Co进行了调查研究;得到核素的区域变化规律和与沉积物性质的相互关系,以及获得各核素的分配系数(K_d)。     

Simplified synthesis of an 8-hydroxyquinoline chelating resin and a study of trace metal profiles from Jellyfish Lake, Palau

We report a simplified synthesis, and some performance characteristics, for 8-hydroxyquinoline (8-HOQ) covalently bonded to a chemically resistant TosoHaas TSK vinyl polymer resin. The resin was used to concentrate trace metals from stored, acidified seawater samples collected from Jellyfish Lake, an anoxic marine lake in the Palau Islands. The Mn, Fe, and Zn profiles determined from the 8-HOQ resin extraction were similar to those determined using Chelex-100 resin. The Zn and Cd profiles did not exhibit removal by sulfide “stripping” in contrast to other anoxic marine basins. The profiles of Co and Ni also exhibited elevated concentrations in the anoxic hypolimnion. The solution speciation and saturation states for the metals were calculated using revised metal-bisulfide stability constants. The calculations suggest that the MS(HS)⁻ species dominates the solution speciation for Mn, Co, Ni, Zn, Cd, and Pb. Cu(I) is modeled as the CuS⁻ or Cu(HS)₂⁻ species, while Fe(II) behaves as the free Fe²⁺ cation. The Mn, Co, Ni, Cu and Cd concentrations appeared to be at least 10-fold undersaturated, while the Fe(II), Zn, and Pb concentrations were close to saturation with respect to their metal sulfides.     

60Co、137Cs在几种海洋生物中浓集问题的初步研究

本文对核电站的主要废物60Co、137Cs在几种海洋生物中的浓集和若干有关的问题进行了初步研究.     

The behavior of Zn,Cd, Cu,Ni, Co,Fe, and Mn in anoxic baltic waters

In June 1981, dissolved Zn, Cd, Cu, Ni, Co, Fe, and Mn were determined from two detailed profiles in anoxic Baltic waters (with extra data for Fe and Mn from August 1979). Dramatic changes across the O₂H₂S interface occur in the abundances of Cu, Co, Fe, and Mn (by factors of ?100). The concentrations of Zn, Cd, and Ni at the redox front decrease by factors between 3 to 5.Equilibrium calculations are presented for varying concentrations of hydrogen sulfide and compared with the field data. The study strongly supports the assumption that the solubility of Zn, Cd, Cu, and Ni is greatly enhanced and controlled by the formation of bisulfide and(or) polysulfide complexes. Differences between predicted and measured concentrations of these elements are mainly evident at lower ΣH₂S concentrations.Cobalt proved to be very mobile in anoxic regions, and the results indicate that the concentrations are limited by CoS precipitation. The iron (Fe²⁺) and manganese (Mn²⁺) distribution in sulfide-containing waters is controlled by total flux from sediment-water interfaces rather than by equilibrium concentrations of their solid phases (FeS and MnCO₃). The concentrations of these metals are therefore expected to increase with prolonged stagnation periods in the basin.     

Particulate manganese and iron in recent sediments of the Gulf of Lions continental margin (north-western Mediterranean Sea): deposition and diagenetic process

This study aims at apprehending the major forcing factors which govern the spatial and vertical Mn and Fe distributions in ten cores from the Gulf of Lions. Speciation by chemical leaching experiments helps understanding their chemical behaviour during the early diagenetic processes in a marine environment under strong continental influence.The distribution and chemical behaviour of Mn and Fe differ drastically. The strong dependence of Mn distribution on chemical conditions is expressed by a marked solid phase Mn enrichment in the oxic layers of sediment deposits. This enrichment increases with decreasing sedimentation rate (increasing water depth). It is illustrated by an enhanced portion of total Mn in the reducible phase and the precipitation of todorokite on calcareous supports in the upper part of the deepest cores. As a result, 65% of the margin total particulate Mn is thought to be stored in slope deposits in a relatively strongly held association. Conversely, the low chemical mobility of iron in the sedimentary column is indicated by uniform depth profiles and an exclusive location in the residual chemical phase in all the studied sites. The Fe distribution is largely controlled by the dispersion of particulate material on the margin from the Rhône River main source.A budget of Mn and Fe accumulation based on the average amount of total Mn and Fe content of sediments deposited during the last 100 yr, has been made taking into account diagenetic readjustments. The total Mn and Fe amount stored on the margin during the last century is estimated to be 1.5×10⁶ and 54×10⁶ t, respectively. These values are seven times higher than the total secular external inputs calculated on the basis of present day riverine and atmospheric fluxes. This large discrepancy is mainly explained by the sharp decrease of the Rhone River discharge after dam buildings between 1950 and 1958. A residual discrepancy dating before 1950, is likely to be due to seafloor erosion and gravity induced mechanisms.     

R/V Isabu-Based First Ultraclean Seawater Sampling for Ocean Trace Elements in Korea

Ocean Science Journal - Trace elements (Mn, Fe, Co, Ni, Cu, Zn, etc.) are essential micronutrients for marine organisms and are thus related to major issues in the ocean, such as climate change,...     

Radiocaesium and 210Pb in Clyde sea loch sediments

Analysis of ²¹⁰Pb, ²²⁶Ra, ¹³⁷Cs and ¹³⁴Cs in short sediment cores provide first estimates of deposition rates in some Clyde sea lochs. The radio-caesium nuclides originate mainly in the liquid effluent released at distance from the Clyde by the Windscale nuclear fuel reprocessing plant and their concentrations in Clyde sediments provide information on (a) enrichment factors onto particulate matter, (b) surficial mixing coefficients and (c) sedimentation rates. A radiocaesium residence time in coastal waters of ca. 10³ years reflects the importance of scavenging by the high nearshore particulate flux. ²¹⁰Pb levels in sediments are controlled, in the unsupported fraction, by a major input sorbed on catchment particulates and, in the supported component, by ²²⁶Ra activities occasionally perturbed by unusually high surface values probably of planktonic origin. In one loch, detectable levels of ¹³⁴Cs and ⁶⁰Co are attributed to their discharge by nuclear submarines.     

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.     

A STUDY ON TRANSFER RULE OF 137Cs AND 60Co IN SEAWATER AND MARINE FOOD WEB

Transfer rule of 137C3 and 60Co in seawater and an arrificial food web which made up of Platy-monas, Arca, tenaeus and Tilapia were studied.The results showed that the transfer of nuclide could be realized in a longer food chain in which seawater contained radioactivity, the transfer along food chain alone was slight, the pathway of nuclide uptaken by organism was mainly from seawater,but the pressnce of the food was helpful to the transfer of the nuclide, the transfer efficiency of 60Co by every member in the marine food chain was greater than that of 137C3.     

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.     

Trends of trace metal (Mn, Fe, Co, Ni, Cu, Zn, Cd and Pb) distributions at the oxic-anoxic interface and in sulfidic water of the Drammensfjord

Anoxic sulfidic waters provide important media for studying the effect of reducing conditions on the cycling of trace metals. In 1987–1988, dissolved and particulate trace metal (Mn, Fe, Co, Ni, Cu, Zn, Cd and Pb) concentrations were determined in the water column of the anoxic Drammensfjord basins, southeastern Norway. The iminodiacetic acid type chelating resin (Chelex 100) was used for the preconcentration of trace metals. The trace metal concentrations were determined using atomic absorption spectrophotometry (AAS), differential pulse polarography (DPP), and differential pulse-anodic stripping voltammetry (DP-ASV).It was observed that the trace metals Mn and Fe were actively involved in the processes of redox cycling (oxidationreduction and precipitation-dissolution) at the O₂/H₂S interface. The dissolved concentrations of Mn, Fe and Co showed maxima just below the O₂/H₂S interface. The seasonal enhancement in the maxima of both dissolved and particulate Mn and Fe at the redox cline is mainly governed by the downward movement of water which carries oxygen. An association of Co with the Mn cycle was observed, while the total dissolved Ni was decreased by only 10–35% in the anoxic waters. The dissolved concentrations of Cu, Zn, Pb and, to a lesser extent, Cd decreased in the anoxic zone.     

微量元素对水库初级生产力的影响

采用生氧量生物测验法对影响水库初级生产力的微量元素进行了测定。结果表明,当氮、磷充足时,锰的限制作用较普遍,而锌、铜的抑制作用也常出现,铁、硒等其他元素在某些条件下也会起限制作用。围隔试验的结果也表明,在施氮、磷的基础上,加施锰剂后,浮游植物生物量（以活性叶绿素ａ表示）增高１．７倍以上,较之单纯施氮、磷肥,生物量亦增高了３５％以上,高峰持续时间约１０ｄ,浮游动物生物量亦有所增加。这些结果都表明锰在提高水库鱼产力中有重要作用,同时也说明在大水域施肥养鱼中添加微量元素是可行的。     

厦门邻近海域海洋环境放射性水平及评价

良好的环境质量是厦门成为一个宜居和滨海旅游城市的重要基石。自日本福岛核事故发生和福建省核电站陆续运行之后,厦门邻近海域潜在的核污染风险受到公众和管理部门的关注。本研究测定了2015年2月和8月厦门邻近海域海水和海洋沉积物中主要放射性核素的含量水平,并据此评价了该海域的环境放射性质量状况。结果表明海水中总铀、90Sr、226Ra、137Cs处于我国海洋放射性水平变化范围以内,无明显季节差异,其他放射性核素58Co、60Co、134Cs、110mAg、59Fe、54Mn、65Zn均未检出,海水中90Sr和137Cs的活度最大值远低于国家海水水质标准限值,海洋沉积物中放射性核素活度水平亦在我国海洋放射性水平变化范围以内。利用我国现有的海洋放射性环境质量评价方法对厦门邻近海域放射性质量状况进行分级评价得出其海水放射性质量为2级,海洋沉积物放射性环境质量为1级,均属于安全级别。研究结果表明2015年在厦门附近海域未观测到放射性污染现象。     

The distribution of Mn,Fe, Zn,Cd and Cu in Baltic seawater; a study on the basis of one anchor station

A total of 150 samples were collected at a 10-days' anchor station in the Bornholm basin (55° 31.1′N, 15° 32.1′E) and analyzed for dissolved (< 0.4 μm) and particulate trace metals. For dissolved Mn, large gradients have been found in the vertical distribution with minimum concentrations (< 0.2 μgl^?1) in the halocline zone and considerably higher values in the deep waters (up to 50 μgl^?1). Ultrafiltration studies indicate that dissolved Mn is probably present as Mn²⁺ in the oxygenated bottom layer. The primary production process was not evident in the particulate Mn profile; the suspended particulate material (SPM), however, shows a considerable enrichment with depth, apparently due to Mn-oxide precipitation.The distribution of dissolved Fe was rather homogeneous, with average concentrations throughout the water column between 0.86 and 1.1 μgl^?1, indicating that the oxidation of Fe²⁺ ions released from the sediments must already be complete in the very near oxidation boundary layer. Relatively high concentrations of particulate Fe were actually measured in the bottom layer, with the maximum mean of 11.2 μgl^?1 at 72 m. Similarly to Mn, the profile of particulate Fe does not reflect the SPM curve of the eutrophic layer. On average, about 70% of the total Fe in surface waters was found to be particulate.The average concentrations of dissolved Zn, Cd and Cu were found to be rather homogeneous in the water column but showed a relatively high variability with time. A simplified model on trace-metal uptake by phytoplankton indicates no significant change in dissolved metal concentrations during the period of investigation. On average, only 1.7% Zn, 3.3% Cd and 9.8% Cu of the total metal concentrations were found in particulate form. SPM analyses showed significant correlations of Zn, Cd and Cu with Fe, indicating that particulate iron is an important carrier for particulate trace metals in Baltic waters.     

Phosphorus and metals bound to organic matter in coastal sediments - An investigation of complexes of P,Cu, Zn,Fe, Mn,Ni, Co and Ti by inductively coupled plasma-atomic emission spectrometry with sephadex gel chromatography

Phosphorus and metals bound to organic matter were separated from coastal sediments of Harima Sound in Seto Inland Sea, Japan by extraction with NaOH and fractionated by Sephadex G-25 chromatography. Phosphorus and metals were determined in the eluates by a multi-channel, inductively coupled plasma-atomic emission spectrometer. Phosphorus and Cu, Zn, Fe, Mn, Ni, Cr, Co and Ti bound to organic matter with high molecular weights (OMHMW) (MW ? 5000) were found to be present in the sediments, but no Mo or V were found. The technique provides minimum estimates of the amounts of P and metals bound to organic matter. These organic complexes show surface enrichment in a sediment core (0–20 cm) and their contents decrease with depth. Also, the amounts of eighteen elements, namely: P, Fe, Mn, Zn, Cu, Si, Al, Ti, Pb, Co, Ni, Cr, Mo, V, Na, K, Ca and Mg, in H₂O, ammonium acetate at pH 7 and 5, hydrogen peroxide, hydroxylamine hydrochloride and hydrogen fluoric acid soluble fractions have been determined with a selective chemical leaching technique for the ²¹⁰Pb-dated sediment core sample. Considerable amounts of P (6–19%) and Cu (5–21%) were associated with organic matter, in contrast to other metals such as Fe, Mn, Zn, Ni, Cr, Co and Ti which were associated with sulfide and silicate.     

Biokinetics of selected heavy metals and radionuclides in two marine macrophytes: the seagrass Posidonia oceanica and the alga Caulerpa taxifolia

Uptake and loss kinetics of Zn, Ag, Cd, ¹³⁴Cs, and ²⁴¹Am by shoots of the seagrass Posidonia oceanica and fronds of the green alga Caulerpa taxifolia were determined in controlled laboratory radiotracer experiments using low contaminant concentrations. The two species accumulated most of the elements efficiently. The only exceptions were ¹³⁴Cs in both P. oceanica and C. taxifolia and Cd in C. Taxifolia (concentration factors 6.4). Steady state in uptake was reached in C. taxifolia for each element except Ag. In P. oceanica, steady state was noted for the uptake of Ag and ¹³⁴Cs whereas Zn, Cd, and ²⁴¹Am were linearly accumulated during the course of the experiment (15 d). With respect to relative metal bioavailability, the different compartments of P. oceanica shoots were generally ranked in the order: leaf epiphytes > adult LEAVES = intermediate leaves > leaf sheaths. The long-lived component of the loss kinetics for each element in P. oceanica was characterized by a relatively short biological half-life (T_b1/2 28 d). However, observations for the individual compartments indicated that adult leaves had a high retention capacity for Ag and ¹³⁴Cs, with virtually 100% retained after 21 d in uncontaminated sea water. In C. taxifolia, the long-lived component of the loss kinetics for each element was characterized by a T_b1/2 value that was not significantly different from infinity, an observation which suggests that a substantial fraction of the metal or radionuclide incorporated during a contamination event would be irreversibly bound by this algal species.     

Surface reactivity of the Rhône suspended matter and relation with trace element sorption

The reactivity of the Rhône estuarine suspended matter is investigated through three operational parameters: the heat of immersion in water (HI), the ammonium saturation index (ASI) and the specific surface area (SSA). The two former parameters are highly correlated for samples collected both in surface river water and in its plume water and in a deeper nepheloid layer. Using both ASI and HI theoretical contributions of each main individual suspended matter component, it is shown that actual and calculated HI values are in agreement, whereas measured ASI values are significantly lower than those calculated. Surface normalization of these reactive properties is discussed on the basis of the SSA measured by the (BET) N2 adsorption. This evaluation, on freeze-dried suspended matter, appears to underestimate the actual particulate reactive surface area in the natural environment; indeed, it is shown that the ammonium ion surfacial density obtained from ASI and SSA data is unrealistically high.To verify that HI and ASI may be considered as criteria for the surface potential reactivity of particles, it has been attempted to relate these parameters and the extent of sorption of radioactive tracer, which is either discharged in the Rhone river or introduced in a batch experiment. Relationships between both ASI and HI and the content of ⁵⁴Mn, ⁶⁰Co, ⁶⁵Zn, ¹⁰⁹Cd and ¹³⁷Cs, which are established for some of them, suggest that HI and ASI are useful indicators of particulate affinity for certain metals.