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1.
Uranium in coastal sediments of Tokyo Bay and Funka Bay   总被引：2，自引：0，他引：2  
The sediment cores from Tokyo Bay and Funka Bay were analyzed for U and its isotopic ratio,234U/238U, after dissolving them in 0.1 M HCl, and 30% H2O2 in 0.05 M HCl. A small fraction of U in the anoxic sediments was dissolved in 0.1M HCl and even the added yield tracer,232U, was lost. The isotopic ratio of H2O2 soluble U in the sediments was equal to that of seawater, suggesting that the H2O2 soluble U in the sediments is authigenic. The 6M HCl solution dissolved part of the lithogenic U besides the authigenic U. The depth profiles of U from the two bays resembled each other. The authigenic U comprised more than half of the total U even at the surface and increased with depth down to 70 cm, showing small maxima at about 20 cm. The concentration of refractory U was nearly constant with depth and similar to that of the pelagic sediments. The highest U concentration, 6 µg g–1 which was about 5 times that of the pelagic sediments, was observed in the layer between 70 and 160 cm depth in Tokyo Bay. The annual sedimentation rates of U in the Tokyo Bay sediments were 2.6 tons at the surface and 7.0 tons at the 70–160 cm depth. The increase in U with depth should be due to the deposition of interstitial U either diffusing downward from the surface indicating the trapping of seawater U, or otherwise diffusing upward from the deeper layer indicating the internal cycling of U within the sediments.  相似文献   

2.
The stability of gypsum in marine sediments has been investigated through the calculation of its saturation index at the sediment in situ temperature and pressure, using the entire ODP/IODP porewater composition database (14416 samples recovered from sediments collected during 95 ODP and IODP Legs). Saturation is reached in sediment porewaters of 26 boreholes drilled at 23 different sites, during 12 ODP/IODP Legs. As ocean bottom seawater is largely undersaturated with respect to gypsum, the porewater Ca content or its SO4 concentration, or both, must increase in order to reach equilibrium. At several sites equilibrium is reached either through the presence of evaporitic gypsum layers found in the sedimentary sequence, and/or through a salinity increase due to the presence of evaporitic brines with high concentrations of Ca and SO4. Saturation can also be reached in porewaters of seawater-like salinity (≈ 35‰), provided sulfate reduction is limited. In this case, saturation is due to the alteration of volcanogenic material which releases large amounts of Ca to the porewaters, where the Ca concentration can reach 55 times its seawater value as for example at ODP Leg 134 site 833. At a few sites, saturation is reached in hydrothermal environments, or as a consequence of the alteration of the basaltic basement. In addition to the well known influence of brines on the formation of gypsum, these results indicate that the alteration of sediments rich in volcanogenic material is a major process leading to gypsum saturation in marine sediment porewaters. Therefore, the presence of gypsum in ancient and recent marine sediments should not be systematically interpreted as due to hypersaline waters, especially if volcanogenic material is present.  相似文献   

3.
Coastal marine sediment, air and seawater samples were collected at six sampling stations in the Eastern Mediterranean Sea distant from pollutant point sources. All sediment samples were analyzed to determine polycyclic aromatic hydrocarbon (PAH), black carbon (BC) and organic carbon (OC) contents. The PAH contents of gaseous and seawater samples of the study were determined in order to evaluate the role of air–sea exchange as PAH nonpoint source to the marine sediments. The average concentration of the total PAHs (∑PAHs) in the sediments varied from 2.2 to 1056.2 ng g−1 dry weight. The average BC and OC contents varied from 0.3 to 5.6 and from 2.9 to 21.4 mg g−1 dry weight, respectively. ∑PAH concentration in the marine atmosphere varied from 20.0 to 83.2 ng m−3. Air–water exchange flux (FA–W) estimation has indicated air transport as a significant source of PAHs to pristine marine sediments of Eastern Mediterranean. In addition, the significant correlation between the PAHs and the organic and soot carbon content further suggests the importance of atmospheric input of PAHs to the sediments.  相似文献   

4.
Chemical extraction techniques show that the majority of the arsenic in North Atlantic deep-sea sediments is associated with an iron phase compositionally similar to that found in deep-sea ferromanganese nodules (As/Fe ～ 11 · 10?4) and is probably of seawater origin. Some sediments also contain As associated with Fe oxides produced by continental weathering. A minority (～8%) of the arsenic is of detrital origin but is not associated with Fe or Mn oxides; it has a content (1.7 ppm) similar to the average crustal abundance. In the Eastern Mediterranean Sea, near-shore sediments contain As associated with land-derived Fe oxides (As/Fe ～ 2 · 10?4), but As/Fe ratios increase to ～ 13 · 10?4 in deep-sea sediments as the contribution of seawater derived arsenic becomes dominant. Arsenic is enriched in metalliferous sediments (As/Fe ～ 20?50 · 10?4) but As/P ratios of metalliferous sediments, deep-sea ferromanganese nodules and deep-ocean water are all similar. Although a hydrothermal contribution cannot be discounted, it is likely that the arsenic is also of seawater origin, suggesting that hydrothermal iron oxyhydroxides remove As more efficiently from seawater than do iron phases (goethite) in deep-sea sediments and nodules. Arsenic accumulates in deep-sea sediments (～ 6 μg cm?2 10?3 yr?1) at sediments (～ 120 μg cm?2 10?3 yr?1) at rate sufficient to balance river input input (～3 · 1010 g yr?1). These estimates give an oceanic residence time for arsenic of 1–2 · 105 yr.  相似文献   

5.
We report the role of particle composition and lateral particle movement that influences the oceanic distribution of 231Pa and 230Th. Settling particles were collected during sediment trap experiments. These and surface sediments were obtained from five stations along 38 to 44°N in the northwestern North Pacific. The high total mass flux and seasonal variations in the marginal area of the western North Pacific are controlled by the supply of lithogenic materials and primary productivity. The high content of the lithogenic material in the settling particles in this area contributes to 230Thex fluxes that exceed the local rate of supply. The lithogenic materials are important as a carrier of 230Th and contribute to the fractionation between 230Th and 231Pa in the ocean, as the 231Paex/230Thex ratio in the settling particles decreases with increasing 232Th concentration. The 231Paex/230Thex ratio in the settling particles collected in the abyssal basin decreases with water depth, which indicates that lateral transport of the lithogenic particles from the marginal area and/or shallower depth plays an important role in determining the 231Paex/230Thex ratio in a population of settling particles and remineralization. This indicates that lateral redistribution of particles and sediment focusing influence the 231Paex/230Thex ratios in surface sediments. Thus, the observations reported here mean that the use of the sediment 231Paex/230Thex ratio as a paleoproductivity proxy will be problematic in the northwestern North Pacific. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

6.
The huge amount of methane hydrate deposits identified in deep marine sediments is considered as the new resource for future energy. Since carbonates are one of the major components of marine sediments, in the present study, an investigation has been made to study methane hydrate stability and kinetics in the presence of CaCO3 and MgCO3. Effect of the presence of carbonates on the solubility of methane in the system has also been examined as it directly affects the hydrate formation process. It has been observed that in presence of CaCO3 and MgCO3, the hydrate formation is inhibited. Comparative studies have also been done in the presence of artificial seawater to consider the effect of presence of different salts. Mole consumption of methane gas during hydrate formation in different carbonate samples was measured using real gas equation and found to be minimum in CaCO3 in seawater sample due to the combined effect of the presence of CaCO3 and different salts of seawater. An increase in nucleation and induction time was also observed demonstrating the inhibition of hydrate formation in the presence of these components. Further, the decrease in hydrate formation rate also confirmed the inhibition effect of CaCO3 and MgCO3 on hydrate formation.  相似文献   

7.
Abstract

The rare earth element (REE) distribution in nine deep-sea ferromanganese nodules and their associated siliceous sediments from the Central Indian Ocean Basin (CIOB) have been studied to elucidate the REE relationship among them. Total REE concentration varies from 398–928 ppm in the nodules and 137–235 ppm in the associated sediments, suggesting two- to four-fold enrichment in the nodules compared to associated sediments. REE of nodules and their associated sediments show a positive correlation, suggesting REE are supplied from a common source such as seawater. The positive correlation between REE of nodules and sediments from the CIOB is contrary to the competitive scavenging of REE between nodules and sediment in the equatorial Pacific Ocean. REEs in the nodules are carried by Fe, P, and Ti, whereas in the sediment they are carried by P and Mn phases. A similar REE fractionation pattern with middle REE enrichment over heavy and light REE in both the nodules and their associated sediment suggest fractionation is independent of REE abundance and their carrier phases.  相似文献   

8.
Ba and Ti in a sediment core (10 m long) from the Okhotsk Sea, covering the last 120 kyrs, were measured. The authigenic Ba (Baex) contents were calculated and compared with the opal. The correlation coefficient between Baex and opal was quite small (r = 0.34), but it greatly grew larger (r = 0.90), if the Baex contents were multiplied by a simple function increasing with depth, except for two intervals. This may be due to the gradual change in the sedimentation environment during the glacial ages. One of the exceptional interval is found at 60–170 cm in depth, corresponding to 10–17 calendar kyr ago, the last termination period of glacial ages, where the Baex began to increase prior to opal. Since the calcium carbonate contents similarly increased prior to the opal increase, the Baex may be also related to calcareous organisms besides siliceous ones. The other is the last interglacial period around 120 kyr ago when the opal contents were high, but those of the Baex were not increased. This can be explained, if the Baex was reduced to sulfide and dissolved away in a strongly anoxic environment during the biologically productive period. During the glacial ages, the mass accumulation rate (MAR) of lithogenic Ti was about twice the amount of that during the interglacial ages. For opal, however, the contrast between the glacial and interglacial ages was more remarkable in its MAR than in its concentration in sediments, due to the larger variation in the bulk sedimentation rates. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

9.
Benzyl butyl phthalate (BBP) is an endocrine-disrupting chemical, and its sorption behaviour on marine sediments was investigated. BBP sorption on the sediments was a rapid process, which could reach equilibrium in 6 h. The sorption equilibrium results could be well described by a linear isotherm. The BBP partition coefficient, Kd, varied from 7.16 to 12.54 L/g in approximately proportion to the organic content of the sediments. After H2O2 oxidation for removing the organic material from the sediments, the Kd values were reduced by more than 70%, but the organic normalised partition coefficient averaged 2165 L/g for the H2O2-treated sediments, which was more than three times of 598 L/g for the raw sediments. The sorption of BBP on the sediments increased with a decrease in temperature and an increase in salinity. A salting constant of 1.14 L/mol was obtained for BBP in artificial seawater. These research findings are of importance to an assessment of the fate and transport of BBP and other similar endocrine-disrupting chemicals (EDCs) in seawater–sediment systems.  相似文献   

10.
Rare earth elements (REEs) of 91 fine-grained bottom sediment samples from five major rivers in Korea (the Han, Keum, and Yeongsan) and China (the Changjiang and Huanghe) were studied to investigate their potential as source indicator for Yellow Sea shelf sediments, this being the first synthetic report on REE trends for bottom sediments of these rivers. The results show distinct differences in REE contents and their upper continental crust (UCC)-normalized patterns: compared to heavy rare earth elements (HREEs), light rare earth elements (LREEs) are highly enriched in Korean river sediments, in contrast to Chinese river sediments that have a characteristic positive Eu anomaly. This phenomenon is observed also in primary source rocks within the river catchments. This suggests that source rock composition is the primary control on the REE signatures of these river sediments, due largely to variations in the levels of chlorite and monazite, which are more abundant in Korean bottom river sediments. Systematic variations in ΣLREE/ΣHREE ratios, and in (La/Yb)–(Gd/Yb)UCC but also (La/Lu)–(La/Y)UCC and (La/Y)–(Gd/Lu)UCC relations have the greatest discriminatory power. These findings are consistent with, but considerably expand on the limited datasets available to date for suspended sediments. Evidently, the REE fingerprints of these river sediments can serve as a useful diagnostic tool for tracing the provenance of sediments in the Yellow Sea, and for reconstructing their dispersal patterns and the circulation system of the modern shelf, as well as the paleoenvironmental record of this and adjoining marginal seas.  相似文献   

11.
The concentration of methane in seawater was determined approximately once a month for one year from August 1990 to July 1991 at a station close to the center of Funka bay (92 m depth) and some supplementary observations were also carried out. The concentration of methane was usually increased with increasing depth, suggesting that methane was emitted from the bottom of the bay. While highly variable both spatially and temporally, the emission was intense in March and April, a period immediately after the spring bloom of phytoplankton. The maximum of methane found in the intermediate water suggests its source from the slope of the bay. The concentration of methane in the surface water changed seasonally and also interannually. The annually averaged flux of methane transferred to the atmosphere in the bay was estimated to be 6×10–3 gCH4m2/day. The coastal zone in the world may be a significant source of the atmospheric methane, although its source strength has yet to be accurately estimated from more data in different coastal seas.  相似文献   

12.
The Tyro and Bannock Basins, which are depressions in the eastern Mediterranean, contain hypersaline anoxic brines. These brines are of different composition: Tyro brine is primarily an early-stage halite (NaCl) brine, whereas Bannock brine includes the more soluble ions of late-stage evaporite minerals. Accordingly, the Bannock brine contains a much greater sulphate concentration than the Tyro Brine. This difference in sulphate concentration is reflected in the concentrations of ions such as Ca, Sr and Ba, which form sparingly soluble sulphate minerals.Equilibrium calculations using the Pitzer specific ion interaction model indicate that the brines in both basins are saturated with respect to gypsum (CaSO4-2H2O) and supersaturated to saturated with respect to dolomite (CaMg(CO3)2). The degree of saturation with respect to dolomite is greater in the Bannock Basin than it is in the Tyro Basin. Correspondingly, recent gypsum crystals and dolomite hardgrounds have been found in the Bannock Basin but not in the Tyro Basin.The Tyro brine is homogeneous in composition, whereas the Bannock brine demonstrates a clear two-layer brine structure. At the interface of the upper and the lower brine distinct positive anomalies occur in the total alkalinity and the concentration of phosphate, and negative anomalies occur in the concentrations of Mn2+ and the rare earth elements (REE). These anomalies and the observed association of gypsum/dolomite in the sediments are all consistent with a recent precipitation of dolomite and gypsum in the Bannock Basin. The brines in both basins are also saturated with respect to barite (BaSO4).The 87Sr/86Sr and δ34S ratios of the Bannock brines are amazingly consistent but differ dramatically from the values for modern or Messinian-age seawater. The Sr concentration and Sr and S isotope ratios in the gypsum crystals indicate that most of these crystals have resulted from precipitation/recrystallization from the brine and not from seawater. The observed variations between crystals are thought to reflect the recrystallization of (sub-) outcropping Messinian gypsum with a low 87Sr/86Sr ratio in the presence of seawater or brine fluids and with different extents of diagenesis.  相似文献   

13.
Accurate knowledge of the extent of biogenic opal preservation in marine sediment cores is important for paleoceanographic reconstructions. The alkaline leaching method is widely employed for %biogenic opal analysis due to its ease and speed. In this study, a revised method for measuring %biogenic opal in sediment from arctic coring expedition samples was suggested. The studied middle Eocene sediments from the central Arctic Ocean presented a problem in insufficiently leaching biogenic opal with a Na2CO3 solution. Based on XRD analysis, it was suggested that such an alkaline resistance results from slight diagenesis of biogenic opal. In order to solve this problem, an alkaline leaching method utilizing a 2 M NaOH solution was suggested for the accurate measurement of %biogenic opal in the Eocene sediments from the central Arctic. Furthermore, dissolution rates from lithogenic matter by NaOH solution were measured in order to correct the %biogenic opal values.  相似文献   

14.
This paper deals with the geochemical characteristics of arsenic in sediments from Bohai Gulf. The arsenic in seawater, surface sediments and cores is determined. Also measured are other physical and chemical parameters, such as Ni, Fe, C, pH and Eh in sediments. The values of As range from 0.6 to 4.5 ppb in seawater, from 10.0 to 20.9 ppm in surface sediments and from 6.8 to 22.8 ppm in cores.The contents of As from south are higher than those from north. However the As in sediments is the element not affected by pollution.The adsorption and codeposition of Ferric oxide colloid are the major form of transference of As from seawater to sediments in Bohai Gulf.The valence state of As in sediments is HAsO42-  相似文献   

15.
《Marine Chemistry》2002,79(1):37-47
Profiles of dissolved organic carbon (DOC) were measured in the pore water of sediments from 1000, 2000 and 3500 m water depth in the eastern North Atlantic. A net DOC accumulation in the pore waters was observed, which followed closely the zonation of microbial respiration in these sediments. The concentration of pore water DOC in the zone of oxic respiration was elevated relative to that in the bottom ocean water. The resulting upward gradient across the sediment–water interface indicated a steady state diffusive benthic flux, FDOC, of 0.25–0.44 mmol m−2 day−1 from these sediments. Subsequent increase in the concentration of DOC in the pore water occurred only in the sediments from 1000 and 2000 m water depth that supported anoxic respiration, leading to a deep concentration maximum. By contrast, in the sediments from 3500 m water depth, a deep concentration minimum was measured, coincident with minimal postoxic respiration in this near-abyssal setting. The gradient-based FDOC represented approximately 14% of the total remineralized organic carbon (TCR=sum of FDOC and depth-integrated organic carbon oxidation rate) in the sediments from 1000 and 2000 m water depth, while it was 36% of the TCR in the sediments from 3500 m water depth. A covariance of particulate organic carbon (POC) and pore water DOC with depth in the sediments was evident, more consistently at the deepest site. While the covariance can be related to biotic processes in these sediments, an alternative interpretation suggests a possible contribution of sorption to the biotic control on sedimentary organic carbon cycling. The steady state diagenetic conditions in which this may occur can be conceivable for some organic-poor deep-sea locations, but direct evidence is clearly required to validate them.  相似文献   

16.
The interaction of Mn2+ with the surface of calcite in aqueous solutions is complex. In dilute solutions the Mn2+ is rapidly absorbed, MnCO33 nucleates on the calcite surface and then grows by a first order reaction with respect to the initial Mn2+ concentration. At higher ionic strengths in NaCl solutions, the rate of these processes is slower, but the same general pattern persists. In solutions containing Mg2+, at the concentration of seawater and in seawater, the nucleation phase of the uptake process does not appear to occur. The long-term uptake rate of Mn2+ on the surface of calcite in seawater is first order with respect to the dissolved Mn2+ concentration. The rate constant is over three orders of magnitude smaller than that found in dilute Mg2+-free solutions. A probable explanation for the slower growth rate in seawater is that MnCO3 is not nucleated on the calcite surface due to the presence of high Mg2+ concentrations. The Mg2+, through site competition, prevents enough Mn2+ from being adsorbed to reach a critical concentration for MnCO3 nucleation. This behavior is similar to that found for orthophosphate with calcite surfaces in dilute solutions and seawater. It indicates that rhodochrosite cannot nucleate in carbonate-rich recent sediments unless the Mg2+ concentration is lowered below that of seawater.Measurements of the solubility of rhodochrosite in seawater gave results from an undersaturation approach to equilibrium in excellent agreement with those found in previous studies in dilute solutions. When equilibrium was approached from supersaturation, approximately fifty times more calcium was precipitated than Mn2+. The measured solubility was over twice that determined from undersaturation. It is possible that a Mn—calcite containing 25 to 30 mol% MnCO3 formed on the rhodochrosite from the supersaturated solutions. Consequently, it is doubtful that pure rhodochrosite controls the concentration of Mn2+ even in calcium carbonate-poor marine environments.  相似文献   

17.
根据2011年6月茅尾海生态环境调查资料,对该海域海水和表层沉积物中叶绿素a的空间分布进行了分析。结果表明,海水叶绿素a变化范围1.384~4.060 mg/m3,平均值为2.143 mg/m3,表层沉积物叶绿素a范围为0.006~0.740 mg/kg(湿重),均值为0.124 mg/kg;海水与表层沉积物叶绿素a均呈现自河口向南逐渐降低的空间分布特征。单位面积表层沉积物叶绿素a平均含量为上方水柱叶绿素a平均含量的129.44%,沉积物对该海域初级生产力有显著的潜在贡献。相关分析表明,海水和沉积物叶绿素a均与无机氮及底栖动物栖息密度呈显著或极显著的正相关关系(P0.05或P0.01)。  相似文献   

18.
1. The adsorption action of basic zinc carbonate adsorbent on uranium in natural seawater can be expressed with the following formula of adsorption isotherm:C=k(U*)n = 8.51× 10-1(U*)0.49,where C is the concentration of uranium on adsorbent; U* is content of uranium in natural seawater employed.2. when the quantity of basic zinc carbonate adsorbent (T) is constant, with the increase of natural seawater quantity through the adsorption column (G), also increased are the adsorption content of uranium of the adsorbent (U), the concentration of uranium on the adsorbent (C) and the concentration of residual uranium (C0*) in natural seawater after adsorbing uranium, while the rate of recovery of uranium (R) is decreased. With the increase of (G) the coefficient of distribution (Kd) decreases to a certain value and then a little rises again.  相似文献   

19.
To understand the transport process of lithogenic particles in the ocean, we measured the grain size distributions of lithogenic particles and measured the opal, La, Yb, Th, and Sc concentrations of the settling particles collected from time-series sediment traps at Sta. KNOT (44°N, 155°E, water depth 5320 m) from June 2002 to May 2004. The annual mean lithogenic particle flux observed at the lower sediment trap (5100 m) was twice as high as that at the upper sediment trap (770 m). The contribution of Asian loess estimated by the La/Yb and the Th/Sc ratios in the lower layer was greater than that in the upper layer. The fluxes of small lithogenic particles with sizes of 3–4 μm at the lower layer (5 to 65 mg/m2/day) were approximately four times larger than that at the upper layer (0.6 to 27 mg/m2/day). These results indicate that the horizontal addition of small particle sizes of Asian loess is a main factor in the increase of lithogenic particles at the lower layer. The temporal variations in the small lithogenic particle flux at the lower layer had a positive correlation with those at the upper layer (r = 0.71). The small lithogenic particle fluxes showed a strong positive correlation with the opal fluxes (r = 0.9). We therefore conclude that the small lithogenic particles were laterally transported and scavenged by the formation of aggregates with opal.  相似文献   

20.
基于全球海洋及其上空大气中关于有机磷酸酯（OPEs）的数据，分析了目前OPEs在全球海洋及其上空大气的分布特征、影响因素以及当前研究存在的不足。总结发现，海水中的OPEs主要来自河流输送，且浓度分布特征表现为由近及远、由浅及深逐渐递减。磷酸三（2-氯乙基）酯（TCEP）、磷酸三（1-氯-2-丙基）酯（TCPP）和磷酸三（1，3-二氯异丙基）酯（TDCPP）三种卤化OPEs是海水中主要污染物；输入到海水中的OPEs经过颗粒沉降等作用沉积到海洋沉积物中，随之，沉积物中的OPEs可能反析出或直接累积，在海洋沉积物中形成一个大的OPEs储存库。分析北太平洋到北冰洋表层沉积物中OPEs的浓度发现，从白令海峡到北冰洋，随着纬度的增加OPEs的浓度也普遍增加，且相对于非卤化OPEs，卤化OPEs更易被运输到偏远海域。总有机碳（TOC）与大洋沉积物中OPEs的浓度无相关性，但与近海海洋沉积物中OPEs的浓度呈正相关，TCEP和磷酸三异丁酯（TiBP）为海洋沉积物中主要污染物；海洋上空大气与水体中的OPEs是不可分割的，海洋上空大气中的OPEs一部分通过大气沉降进入海水，一部分继续迁移到更偏远区域，气团来源是影响其分布的主要因素。对比OPEs在全球海洋上空大气中的浓度分布发现，南北半球并无明显差异，TCEP和TCPP是海洋上空大气中主要污染物。  相似文献   

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