用镭同位素评价胶州湾水体表观年龄及地下水入海通量

为评价胶州湾水体表观年龄和地下水入海通量,2011年9—10月在胶州湾地区分别采集地下水、河水和海水样品,对水样的224Ra和226Ra活度进行测量。基于224Ra和226Ra半衰期的差异,运用224Ra与226Ra的活度比值计算了胶州湾水体表观年龄;采用三端元混合模型计算了胶州湾海水中地下水、河水与湾外海水的混合比例;在水体表观年龄和混合比例的基础上,计算了地下水入海通量。结果表明:研究期间胶州湾水体表观年龄分布范围为3.2—39.4d,平均值为14.7d,呈现从湾顶到湾口年龄逐渐增大的趋势,地下水的平均混合比例是11.0%,地下水的入海通量为7.29×106m3/d,海底地下水排泄速率为3.8cm/d。     

Radium and radon radioisotopes in regional groundwater, intertidal groundwater, and seawater in the Adelaide Coastal Waters Study area: Implications for the evaluation of submarine groundwater discharge

The input of groundwater-borne nutrients to Adelaide's (South Australia) coastal zone is not well known but could contribute to the ongoing decline of seagrass in the area. As a component of the Adelaide Coastal Waters Study (ACWS), the potential for using the radium quartet (²²³Ra, ²²⁴Ra, ²²⁶Ra and ²²⁸Ra) and ²²²Rn to evaluate submarine groundwater discharge (SGD) was evaluated. Potential isotopic signatures for SGD were assessed by sampling groundwater from three regional aquifers potentially contributing SGD to the ACWS area. In addition, intertidal groundwater was sampled at two sand beach sites. In general, the regional groundwaters were enriched in long-lived Ra isotopes (²²⁶Ra and ²²⁸Ra) and in ²²²Rn relative to intertidal groundwater. Radium activity (but not ²²²Rn activity) was positively correlated to salinity in groundwater from one of the regional aquifers and in intertidal groundwater. Radium isotope ratios (²²³Ra/²²⁶Ra, ²²⁴Ra/²²⁶Ra and ²²⁸Ra/²²⁶Ra) were less variable than individual Ra isotope activities within potential SGD sources. Recirculated seawater (estimated from the intertidal groundwater samples with seawater-like salinities) also had distinctly higher Ra isotope ratios than the regional groundwaters. The activities for all radioisotopes were relatively low in seawater. The activity of the short-lived ²²³Ra and ²²⁴Ra were highest at the shoreline and declined exponentially with distance offshore. In contrast, ²²⁸Ra and ²²⁶Ra activities had a weak linear declining trend with distance offshore. Rn-222 activity was at or near background in all seawater samples. The pattern of enrichment in short-lived Ra isotopes and the lack of ²²²Rn in seawater suggest that seawater recirculation is the main contributor to SGD in the ACWS area. Preliminary modeling of the offshore flux of ²²⁸Ra and ²²⁶Ra suggest that the SGD flux to the ACWS area ranges between 0.2 and 3 · 10^− 3 m³ (m of shoreline)^− 1 s^− 1.     

High-precision measurement of oceanic 226Ra

A system capable of oceanic ²²⁶Ra measurements with a precision of ±1% is described, which represents an improvement of approximately a factor of three over existing techniques. ²²²Rn grown-in from ²²⁶Ra decay in 14-l seawater samples is quantitatively transferred to, and measured in, proportional gas counters. Errors other than counting statistics are estimated not to exceed ±0.5%, which is consistent with repeated ²²⁶Ra measurements on the same samples. A NE Atlantic ²²⁶Ra depth profile (2000–5000 m) is reported as an example. It is found that with the precision reported here, certain hitherto unresolved features of the ²²⁶Ra distribution in deep water become apparent.     

Comparison of techniques for pre-concentrating radium from seawater

In the framework of the KEOPS project (KErguelen: compared study of the Ocean and the Plateau in Surface water), we aimed to provide information on the water mass pathways and vertical mixing on the Kerguelen Plateau, Southern Ocean, based on ²²⁸Ra profiles. Because ²²⁸Ra activities are extremely low in this area (~ 0.1 dpm/100 kg or ~ 2.10^− 18 g kg^− 1), the filtration of large volumes of seawater was required in order to be able to detect it with minimal uncertainty. This challenging study was an opportunity for us to test and compare methods aimed at removing efficiently radium isotopes from seawater. We used Mn-fiber that retains radium and that allows the measurement of all four radium isotopes (²²⁶Ra, ²²⁸Ra, ²²³Ra, ²²⁴Ra). First, we used Niskin bottles or the ship's seawater intake to collect large volumes of seawater that were passed onto Mn-fiber in the laboratory. Second, we filled cartridges with Mn-fiber that we placed in tandem on in situ pumps. Finally, we fixed nylon nets filled with Mn-fiber on the frame of in situ pumps to allow the passive filtration of seawater during the pump deployment.Yields of radium fixation on the cartridges filled with Mn-fiber and placed on in situ pumps are ca. 30% when combining the two cartridges. Because large volumes of seawater can be filtered with these pumps, this yields to effective volumes of 177–280 kg (that is, higher than that recovered from fourteen 12-l Niskin bottles). Finally, the effective volume of seawater that passed through Mn-fiber placed in nylon nets and deployed during 4 h ranged between 125 and 364 kg. Consequently, the two techniques that separate Ra isotopes in situ are good alternatives for pre-concentrating radium from seawater. They can save ship-time by avoiding repeated CTD casts to obtain the large volumes of seawater. This is especially true when in situ pumps are deployed to collect suspended particles. However, both methods only provide ²²⁸Ra/²²⁶Ra ratios. The determination of the ²²⁸Ra specific activity is obtained by multiplying this ratio by the ²²⁶Ra activity measured in a discrete sample collected at the same water depth.     

Measurement of 224Ra, 226Ra and 228Ra in seawater using Mn-fiber adsorption-γ spectrum method

I~IOXThe half-lives of natural radioactive nuclides "'Ra, 226Ra and 228Ra are 3. 66 d, 5. 76 a,1600 a respectively, hence, the marine process with various time scales can be researched by taking these nuclides as tracers. Because these nuclides can be determined by measuring them or theirdaughters' a,g, y-rays, they have been applied extensively in oceanography research. Huang(1996), Huang et al. (1996 a,b) and Chen (1996) have given reviews on it.Since the contents of "'Ra, 226Ra and 228…     

北黄海水体的226Ra和228Ra

用锰纤维富集-射气法测定了北黄海海水中的镭同位素226Ra和228Ra,研究了该海域水体中镭同位素的含量和分布.研究结果表明北黄海水体夏季226Ra的比活度为1.80～4.35 Bq/m3,平均值为3.06 Bq/m3;冬季226Ra的比活度为2.08～5.20 Bq/m3,平均值为3.28 Bq/m3.北黄海夏季228Ra的比活度为3.85～25.60 Bq/m3,平均值为10.60 Bq/m3;冬季228Ra的比活度为3.14～15.60Bq/m3,平均值为7.66 Bq/m3.该数据范围和中国近海其他海域、孟加拉湾、泰国昭披耶河口、濑户内海等海域相近.北黄海东北部海域,渤海海峡靠近山东半岛的海区和中北部海区表层镭同位素活度较高.C1断面镭同位素的分布特征从镭同位素的方面证实了渤海海峡水交换表现为北进南出特征这一结论的正确性.226Ra和228Ra的垂直分布较为复杂,大部分站位呈现出底层活度变高的趋势,其他少数站位呈现出中间层活度高的分布特征,不同来源的镭同位素输入至该海域形成了这样的分布特征.     

A practical method for the simultaneous determination of234Th,226Ra,210Pb and210Po in seawater

A practical method has been developed for the simultaneous determination of²²⁶Ra,²³⁴Th,²¹⁰Pb and²¹⁰Po in seawater. In the method, the samples are spiked with²²⁸Ra,²³⁰Th,²⁰⁸Po and common lead to determine chemical yield. These nuclides are coprecipitated with calcium carbonate and ferric hydroxide from 20 to 50 l of seawater and separated from one another by using coprecipitation and ion exchange techniques. Counting sources of Ra and the other nuclides are prepared by electrodeposition onto silver discs. Their radioactivities are counted with an-spectrometer and a low background-counter. This method gives a standard deviation of about 5% for replicate determination of²²⁶Ra and the other nuclides.     

Radium tracing of submarine groundwater discharge (SGD) and associated nutrient fluxes in a highly-permeable bed coastal zone, Korea

In order to estimate submarine groundwater discharge (SGD) and SGD-driven nutrient fluxes, we measured the concentrations of nutrients, ²²⁴Ra, and ²²⁶Ra in seawater, river water, and coastal groundwater of Yeongil Bay (in the southeastern coast of Korea) in August 2004 and February 2005. The bottom sediments over the shallow areas of this bay are composed mainly of coarse sands. Large excess concentrations of ²²⁴Ra, ²²⁶Ra, and Si supplied from SGD were observed in August 2004, while these excess concentrations were not apparent in February 2005. Based on the mass balance for ²²⁴Ra, ²²⁶Ra, and Si, which showed conservative mixing behavior in seawater, SGD was estimated to be approximately 6 × 10⁶ m³ day^− 1 (seepage rate = 0.2 m day^− 1) in shallow areas (< 9 m water depth) in August 2004, which is much higher than the SGD level typically found in other coastal regions worldwide. During the summer period, SGD-driven nutrients in this bay contributed approximately 98%, 12%, and 76% of the total inputs for dissolved inorganic nitrogen (DIN), phosphorus (DIP), and silicate (DSi), respectively. Our study implies that the ecosystem in this highly permeable bed coastal zone is influenced strongly by SGD during summer, while such influences are negligible in winter.     

应用镭-226解读南极普里兹湾表层水的来源与运移

中国第22次南极科学考察航次(2005年12月至2006年1月)期间,利用Mn-纤维富集大体积表层海水中的Ra同位素,并通过222Rn直接射气法测量226Ra的比活度,结果表明,普里兹湾表层水的226Ra比活度变化为0.92~2.09 Bq/m3,平均值为1.61 Bq/m3,在深海区域表现出226Ra含量高的特征。从空间分布看,表层水226Ra比活度呈现出由湾内向湾外增加的反常态势,反映出不同Ra含量水团的混合影响2。26Ra比活度与盐度的关系证实研究海域表层水的Ra含量主要受三种端元水体的混合所控制:其一为具有镭含量高、盐度高特征的南极夏季表层水;其二为低镭、低盐特征的冰融水;其三为高盐、中等镭含量的普里兹湾中深层水,该水体的226Ra纯粹由海底沉积物间隙水向上扩散所维持。结合S-226Ra示踪体系及上述三端元混合模型,计算出各组成水体的比例并描绘出它们的空间分布。南极夏季表层水的份额由湾外向湾内逐渐降低,并且在68°E断面向南影响范围较大;冰融水的比例由湾内向湾外降低,并且在湾内东部的高温水体中具有最大贡献;普里兹湾中深层水中受沉积物镭来源影响比较显著的区域出现在湾内西北部,其影响向湾外逐渐降低。冰融水与普里兹湾中深层水份额分别于普里兹湾湾顶东、西部出现高值的分布特征证实埃默里冰架前沿海流东进、西出的运移规律。     

南极普里兹湾及其邻近海域表层水镭同位素的分布及应用

中国第27次南极科学考察期间(2010年12月30日至2011年1月16日),对普里兹湾及其邻近海域表层海水进行了226Ra和228Ra的分析,结果表明:226Ra和228Ra比活度的变化范围分别为1.47—2.43Bq/m3和0.17—0.45Bq/m3,平均值分别为2.13Bq/m3和0.29Bq/m3,228Ra/226Ra)A.R.(228Ra与226Ra的活度比)的变化范围为0.08—0.20,平均值为0.14。根据盐度和226Ra的质量平衡方程,计算出研究海域表层水中冰融水、南极夏季表层水和普里兹湾中深层水的份额。研究海域表层水中温度、盐度、226Ra、228Ra、228Ra/226Ra)A.R.和冰融水份额的空间分布显示,在埃默里冰架前沿海域,西侧海域较东侧海域具有低温、高盐、高226Ra、低228Ra、低228Ra/226Ra)A.R.、低冰融水份额的特征,证实埃默里冰架下水体东进西出的运动规律。根据埃默里冰架前沿东、西侧水体228Ra/226Ra)A.R.的差异,估算出埃默里冰架下表层水体东进西出所经历的时间为1.85a。此外,在普里兹湾湾口中部海域(66.5—67.5°S,72°—74°E),观察到次表层水的上升通风作用,该区域较高的228Ra含量和228Ra/226Ra)A.R.证明这些表层水体并非来自湾外绕极深层水的上涌,而可能来自湾内埃默里冰架输出水体。