厦门岛南岸地下水的氢氧同位素的示踪研究

实测了厦门岛沿岸地区地下水的氢、氧稳定同位素组成，并据此开展了沿岸地下水水文学的同位素示踪研究。对地下水、海水及大气降水的δD～δ^18O方程进行数理分析后表明，大气降水是厦门沿海浅层地下水的主要来源。利用稳定同位素质量平衡模型，估算9810号台风所致降水对地下水的贡献。结合水文资料，通过地下水氢、氧同位素组成的时空分布特征，验证了地下水由北向南运移并最终排入沿岸海域的运移途径。研究还初步探讨了地下水稳定同位素组成对潮汐变化的响应。     

厦门大气降水的氢氧同位素研究

本文研究了厦门地区大气降水的氢、氧同位素组成,提出了大气降水线方程的δD＝8．16δ^18O＋10．68,并与全国及全球降水线进行比较,揭示了该降水线方程的特征。对全年氚过剩值（d）及降水线特征研究表明,厦门岛全年降不涞源较为单一,主要为海洋性气团。降水中δD与δ^18O的降水量效应明显,且该影响远远掩盖了温度效应。     

深海锰结核中铀、钍分离与测定新方法的研究

本文研究了铀和钍在HNO₃-NH₄NO₃体系中的阴离子交换分离,提出了仅用一根离子交换柱就能从深海锰结核这种复杂体系中有效地分离出微量的放射化学纯的铀和钍的新方法。结果表明HNO₃-NH₄NO₃体系阴离子交换分离铀和钍具有较高的选择性,而且体系的酸度下降或硝酸铵浓度提高均有利于铀或钍在树脂相的吸附。该分离方法可定量回收锰结核样品中的铀和钍,且流程简短、操作方便,特别适用于成批的海洋环境样品的分析。     

垂直集成采样法在234Th—238U不平衡研究海洋新生产力中的应用

对基于梯形积分原理的集成采样法的可行性在理论上进行了阐述,并在厦门湾和南海北部的5个站位分别采集不同深度的水样和由这些水样按一定比例混合而成的集成水样进行了现场研究,结果表明两种采样方法经不可逆稳态清除模型得出的溶解态234Th的清除通量、颗粒态234Th的输出通量及溶解态、颗粒态234Th的停留时间基本一致,证实了垂直集成采样法的可行性与可靠性。这种新的采样方案为今后充分发挥234Th法的优势,在更大空间尺度上进行新生产力的研究提供了可靠的保证。     

锰纤维富集-γ能谱法测定海水中的224Ra、226Ra和228Ra

采用锰纤维富集大体积海水中的镭同位素,继用HPGey谱仪通过测定子体发射的y射线测定了海水中224Ra、226Ra和228Ra的比活度.推导了3种核素比活度的计算公式,讨论了样品处理和谱分析方法.该法简单、快速,省却了化学分离的繁杂过程,可同时测定3种核素.     

南极普里兹湾及其邻近海域溶解有机碳的分布

中国南极科学考察第16航次期间(1999年11月～2000年4月),在南极普里兹湾及邻近海域的不同站位与水深采集海水样品用于溶解有机碳测定,通过高温催化氧化法完成样品的分析.结果表明,在调查期间,南极普里兹湾及其邻近海域各测站上层水体(0～100m)溶解有机碳浓度的变化范围为14.3～181.1μmol/dm3,平均为52.5μmol/dm3,该变化幅度比Ross海、太平洋等海域的相应值略大.溶解有机碳垂直分布的特征是0大于25大于50大于100m,即随深度的增加溶解有机碳浓度逐渐减小,与生物活动在垂直方向上的强弱变化相关.根据200m以深水柱溶解有机碳的垂直分布,可确定研究海域难降解溶解有机碳的浓度为40.4μmol/dm3,与其他研究所报道的数值(～42μmol/dm3)相近.上层水体(0～100m)过剩溶解有机碳的空间分布显示,64°S以北海域溶解有机碳过剩较多,而64°S以南海域则过剩溶解有机碳较少.溶解有机碳浓度与分布特征显示,普里兹湾及其邻近海域溶解有机碳浓度与南大洋其他海域相当,具有低溶解有机碳的一般特征.溶解有机碳浓度的空间分布呈现由西南向东北方向逐渐增加的趋势,这可能与南极陆架夏季上层水的北向扩展有关.生物活动及水体运动是研究海域溶解有机碳分布的主要影响因素.     

北太平洋亚热带环流区表层水的210Po/210Pb不平衡

对北太平洋亚热带环流区表层水中溶解态(＜0.2 μm)和颗粒态(≥0.2 μm)210 Po、210pb的含量、分布、停留时间及其在颗粒物清除迁出过程中的分馏效应开展了研究,结果表明,研究海域表层水中溶解态210Po、210Pb的比活度分别介于0.14 ～3.75和1.41 ～6.87 Bq/m3之间;颗粒态210Po、210Pb的比活度分别介于0.35 ～ 2.49和0.18 ～3.18 Bq/m3之间.溶解相和颗粒相中的210Po/210Pb不平衡状态呈现截然不同的特征,溶解相中210Po相对于210Pb呈亏损状态,而在颗粒相中则呈过剩状态,反映出210Po与210Pb生物地球化学行为的差异,210Po具有更强的颗粒(生物)活性.由稳态不可逆模型计算出溶解态和颗粒态210Po的平均停留时间分别为0.28、0.27 a;溶解态和颗粒态210Pb的平均停留时间分别为0.88、0.15 a.由清除速率常数法计算得到的溶解态210Po、210Pb在颗粒清除过程中的平均分馏因子为4.73,且该分馏因子随颗粒氮含量的增加呈增加的趋势.停留时间的差异以及明显大于1的分馏因子均表明,210Po、210Pb在颗粒清除过程中发生了明显的分馏,而分馏因子与颗粒氮(PN)之间存在的正相关关系则显示含氮组分对210 Po、210Pb的分馏起着一定的作用.     

Seasonal export fluxes of size-fractionated particulate derived from polonium-210: A case study in Xiamen Bay

Size-fractionated 210Po and 210Pb, in the size fractions 0.4 μm, 2 μm and 10 μm, were examined to determine the seasonal variability of particulate fluxes in Xiamen Bay. Good correlations between 210Po and particulate organic carbon (POC) or non-Particulate Organic Matter (nPOM) suggested that 210Po can be used to trace the export fluxes of POC and nPOM. Both steady-state (SS) model and nSS model were used to evaluate fluxes of size-fractionated 210Po, results showed that nSS model was better than the SS model in coastal areas. Based on the nSS model, size-fractionated POC fluxes decreased with increasing particle size. For the particle size studied, maximum POC fluxes occurred in autumn, followed by spring, winter, and summer. Fluxes of nPOM were an order of magnitude higher than the corresponding size-fractionated POC fluxes. Differences between size-fractionated nPOM fluxes indicated that hydrodynamic conditions were the main factor regulating transportation of particulate out of the inner Bay. In winter most particulates, including 10 μm particles, were transported under the strongest hydrodynamic conditions. In contrast, only a fraction of the 2 μm particulates were transported from the inner Bay in spring. This study suggested that 210Po is a powerful tracer of seasonal particulate export in coastal seas.     

Seasonal export fluxes of size-fractionated particulate derived from polonium-210: A case study in Xiamen Bay

Size-fractionated ²¹⁰Po and ²¹⁰Pb, in the size fractions >0.4 μm, >2 μm and >10 μm, were examined to determine the seasonal variability of particulate fluxes in Xiamen Bay. Good correlations between ²¹⁰Po and particulate organic carbon (POC) or non-Particulate Organic Matter (nPOM) suggested that ²¹⁰Po can be used to trace the export fluxes of POC and nPOM. Both steady-state (SS) model and nSS model were used to evaluate fluxes of size-fractionated ²¹⁰Po, results showed that nSS model was better than the SS model in coastal areas. Based on the nSS model, size-fractionated POC fluxes decreased with increasing particle size. For the particle size studied, maximum POC fluxes occurred in autumn, followed by spring, winter, and summer. Fluxes of nPOM were an order of magnitude higher than the corresponding size-fractionated POC fluxes. Differences between size-fractionated nPOM fluxes indicated that hydrodynamic conditions were the main factor regulating transportation of particulate out of the inner Bay. In winter most particulates, including >10 μm particles, were transported under the strongest hydrodynamic conditions. In contrast, only a fraction of the <2 μm particulates were transported from the inner Bay in spring. This study suggested that ²¹⁰Po is a powerful tracer of seasonal particulate export in coastal seas.     

东太平洋多金属结核中放射性核素的不破坏γ谱分析

用HPGeγ谱仪不破坏地直接测定了采自东太平洋的20个多金属结核样品,样品中可探测到的核素有238U,230Th,226Ra,210Pb,228Ra,228Th,235U,227Ac(或231Pa)和40K.对样品顶侧和底侧分别面对探测器的计数率和计数率比进行了分析,获得了其所蕴含的多金属结核生长、运动、放射性核素来源及其与环境关系的信息.提出了判断多金属结核顶、底侧的新方法.并根据顶、底侧230Th计数率比推测多金属结核不同的滚动时间.