东海内陆架沉积物敏感粒级构成及其地质意义

沉积物粒级包含了大量的沉积环境信息,在古环境恢复和重建中被广泛应用。基于采自东海内陆架的三根沉积物岩芯,作者利用激光粒度分析方法研究了沉积物的粒度组成,确定了敏感性粒级,探讨了搬运机制及其环境意义。研究表明:东海内陆架现代沉积物含有大致相同的三个敏感性粒级,分别是粒级1(12μm)、粒级2(12—225μm)和粒级3(225μm)。从北到南敏感粒级具有逐渐细化的趋势,该趋势与长江入海沉积物向南搬运过程中发生的沉积分异作用有关。粒级1和粒级2分别由均匀悬浮次总体和递变悬浮次总体构成,而粒级3则由生物过程产生。结合该区的海洋动力特征,作者认为,粒级2可较好地用来指示冬季海洋动力强度,并具有揭示东亚冬季风强度的潜在意义。     

近60年来长江河口河势变化及其对水动力和盐水入侵的影响I.河势变化

河势是影响河口水动力和盐水入侵基本因子。本文利用20世纪50和70年代长江河口海图,数值化岸线和水深,结合2012年长江河口实测水深资料,分析长江河口自50年代以来的河势变化。长江河口为分汊河口,50年代仅为二级分汊,至70年代才形成三级分汊,四口入海的河势格局。70年代相比于50年代,北支淤浅严重,其上、中、下段容积变化分别为-64.13×106、-306.60×106和-639.27×106 m3,对应的变化率分别为-16.30%、-22.74%和-25.69%,均显著减小;南支的上、中、下段容积变化分别为-28.61×106、-35.69×106和126.43×106 m3,相应的变化率分别为-1.30%、-2.12%和4.36%;北港由于崇明浅滩和横沙浅滩的淤浅,下段容积明显减小,其上段和下段容积变化分别为109.21×106和-797.14×106 m3,对应的变化率分别为5.01%和-15.25%;南港上段由于河道淤浅容积减小,下段北由于铜沙浅滩被冲开形成北槽,导致水深变深、容积增加,其上段、下段北和下段南容积变化分别为-238.95×106、203.58×106和153.34×106 m3,对应的变化率分别为-8.96%、6.85%和3.26%。2012年相比于70年代,北支由于大量淤浅和围垦容积大幅减小,其上、中、下段容积变化分别为-199.06×106、-504.61×106和-654.12×106 m3,对应的变化率分别为-60.45%、-48.44%和-35.38%;南支的上、中、下段容积变化分别为92.34×106、193.01×106和-163.62×106 m3,相应的变化率分别为4.24%、11.73%和-5.40%;北港上段青草沙水库的围垦和下段横沙东滩的围垦造成面积和容积减小,其上段和下段容积变化分别为-154.64×106和-511.79×106 m3,对应的变化率分别为-6.75%和-11.55%;南港由于上段河道刷深而下段九段沙以及南汇边滩淤浅、围垦,导致其容积上段增加,下段减小,上段、下段北和下段南容积变化分别为136.39×106、-658.28×106和-1266.11×106 m3,对应的变化率分别为5.62%、-20.73%和-26.06%。     

胶州湾沉积物重金属形态不同浸取方法的比较与污染讯息指示作用初探

海洋沉积物中重金属的活性形态对于指示沉积物污染状况具有重要作用;为探寻简洁且能够有效提取重金属活性形态的浸提方法;实验研究了0.1 mol/L和1 mol/L盐酸的单级提取和欧共体标准局（European Community Bureau of Reference）提出的BCR分级提取法对胶州湾表层沉积物中重金属（Cr、Cu、Ni、Pb、Zn）和Al、Fe、Mn的浸取效果。结果显示;3种提取方法提取的金属含量呈显著正相关关系;两种浓度的稀盐酸对BCR方法中的酸可提取态和可还原态金属均具有较好浸提效果;但对可氧化态金属浸提能力相对较弱。不同提取方法的人为信号指数（ASI）计算结果表明;BCR浸取法提取结果的金属ASI值最大;表明其对沉积物中金属活性形态提取效率较高;1 mol/L HCl提取结果的金属ASI值最低;可能是较高浓度强酸使沉积物较大颗粒内层中“惰性”金属被浸取出来;“增加”了金属活性组分的污染讯息信号;对沉积物中Cu、Pb和Zn而言;0.1 mol/L HCl提取结果的ASI值与BCR方法接近。经过Al归一化后;0.1 mol/L HCl浸提的重金属含量的空间分布与胶州湾的实际污染状况相吻合;表明0.1 mol/L的HCl在一定程度上能够代替复杂的BCR浸取法;此方法可简化重金属活性形态的提取步骤;适合大范围沉积物重金属污染评价。     

The Air-Coastal Sea Chemical Exchange: A Case Study on the New Jersey Coast

The coastal marine atmosphere adjacent to large urban and industrial centers is in general strongly impacted by pollution emissions, resulting in high loading of pollutants in the ambient air. Among the airborne substances are certain trace elements from a variety of emission sources that can serve as micronutrients to marine organisms in coastal waters. High concentrations of such elements in coastal air can result in enhanced air-to-sea deposition fluxes to coastal waters. They could also be transported over the open ocean, affecting the composition of the remote marine atmosphere and then ocean ecosystems. To provide better understanding of the extent of air-to-sea deposition processes on the New Jersey coast, a heavily polluted coastal region on the US East Coast, a synthesis of observation data was carried out for selected trace elements, including Fe, Cd, Cr and Cu, derived from measurements of both size-segregated and bulk aerosol particles, as well as precipitation around the New Jersey coast. The atmospheric input of Hg was also estimated based on measurement data. Results indicated that the total deposition fluxes of most trace elements were higher in Northern coastal NJ compared to Southern coastal NJ, reflecting the differences in the source strengths of these element emissions between the two coastal regions. Dry deposition processes were more significant for common dust-derived elements, particularly Fe and Al, compared with their wet deposition fluxes. However, the processes of precipitation scavenging appeared to be more important for the elements that were often enriched in fine particles including Zn, Cu, Pb and Ni. The removal of Hg from the ambient air was overwhelmingly dominated by atmospheric wet deposition. In the future, atmospheric measurements at more sites on the NJ coast should be performed simultaneously to reduce the spatial and temporal uncertainties associated with atmospheric deposition fluxes estimated in this study.     

The removal kinetics of dissolved organic matter and the optical clarity of groundwater

Concentrations of dissolved organic matter (DOM) and ultraviolet/visible light absorbance decrease systematically as groundwater moves through the unsaturated zones overlying aquifers and along flowpaths within aquifers. These changes occur over distances of tens of meters (m) implying rapid removal kinetics of the chromophoric DOM that imparts color to groundwater. A one-compartment input-output model was used to derive a differential equation describing the removal of DOM from the dissolved phase due to the combined effects of biodegradation and sorption. The general solution to the equation was parameterized using a 2-year record of dissolved organic carbon (DOC) concentration changes in groundwater at a long-term observation well. Estimated rates of DOC loss were rapid and ranged from 0.093 to 0.21 micromoles per liter per day (μM d^?1), and rate constants for DOC removal ranged from 0.0021 to 0.011 per day (d^?1). Applying these removal rate constants to an advective-dispersion model illustrates substantial depletion of DOC over flow-path distances of 200 m or less and in timeframes of 2 years or less. These results explain the low to moderate DOC concentrations (20–75 μM; 0.26–1 mg L^?1) and ultraviolet absorption coefficient values (a ₂₅₄?<?5 m^?1) observed in groundwater produced from 59 wells tapping eight different aquifer systems of the United States. The nearly uniform optical clarity of groundwater, therefore, results from similarly rapid DOM-removal kinetics exhibited by geologically and hydrologically dissimilar aquifers.     

格尔木河流域河水钾硼锂元素分布特征及富集规律

在柴达木格尔木河流域,随着内陆流域水系的产生与地表径流的消亡,从山区至盐湖区钾(K)硼(B)锂(Li)等有益元素的分布可以划分为淋溶-径流区、径流-蒸发区与溶滤-蒸发浓缩富集区3个具有显著特点的水文化学分带。河水中,K、B、Li含量随矿化度升高而升高,且呈正相关关系。在盐湖区,K、B、Li等资源性元素明显富集。研究发现,格尔木河东部主流(秀水河)是格尔木河水中B和Li的主要贡献者。     

矿业权边界在资源储量估算垂直纵投影图上的确定

利用垂直纵投影图进行资源储量估算时,当矿体走向与矿业权边界斜交时,矿业权边界在资源储量垂直纵投影图上投影的准确位置较难确定。该文介绍了利用不同中段平面图和利用计算公式确定矿业权边界在资源储量垂直纵投影图上的投影位置,对解决此类问题具有一定的参考价值。     

Zircon M127 – A Homogeneous Reference Material for SIMS U–Pb Geochronology Combined with Hafnium,Oxygen and,Potentially, Lithium Isotope Analysis

In this article, we document a detailed analytical characterisation of zircon M127, a homogeneous 12.7 carat gemstone from Ratnapura, Sri Lanka. Zircon M127 has TIMS‐determined mean U–Pb radiogenic isotopic ratios of 0.084743 ± 0.000027 for ²⁰⁶Pb/²³⁸U and 0.67676 ± 0.00023 for ²⁰⁷Pb/²³⁵U (weighted means, 2s uncertainties). Its ²⁰⁶Pb/²³⁸U age of 524.36 ± 0.16 Ma (95% confidence uncertainty) is concordant within the uncertainties of decay constants. The δ¹⁸O value (determined by laser fluorination) is 8.26 ± 0.06‰ VSMOW (2s), and the mean ¹⁷⁶Hf/¹⁷⁷Hf ratio (determined by solution ICP‐MS) is 0.282396 ± 0.000004 (2s). The SIMS‐determined δ⁷Li value is ?0.6 ± 0.9‰ (2s), with a mean mass fraction of 1.0 ± 0.1 μg g^?1 Li (2s). Zircon M127 contains ~ 923 μg g^?1 U. The moderate degree of radiation damage corresponds well with the time‐integrated self‐irradiation dose of 1.82 × 10¹⁸ alpha events per gram. This observation, and the (U–Th)/He age of 426 ± 7 Ma (2s), which is typical of unheated Sri Lankan zircon, enable us to exclude any thermal treatment. Zircon M127 is proposed as a reference material for the determination of zircon U–Pb ages by means of SIMS in combination with hafnium and stable isotope (oxygen and potentially also lithium) determination.