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1.
盐度对镭同位素在海南红树林沉积物解吸行为的影响 总被引：1，自引：0，他引：1
天然放射性镭同位素在沉积物上的解吸行为是影响其在陆-海交换过程中的关键所在。采用沉积物室内解吸实验和现场采集间隙水测量224Ra含量两种方法,对水体盐度梯度控制镭在海南八门湾红树林沉积物的解吸行为进行了讨论。结果表明:沉积物上可交换态224Ra的最大量为0.44dpm/g,解吸比为35%。利用间隙水的224Ra含量确定镭的分配比Kd与水体盐度S呈反比例函数:Kd=8.4×102/S,与室内解吸实验的结果相比更能代表镭在沉积物上的真实解吸行为。在深度25—40cm内,湿地沉积物的224Ra处于与其母体228Th的平衡状态,但223Ra很可能处于相对其母体227Th亏损状态。 相似文献
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基于223Ra和224Ra的桑沟湾海底地下水排放通量 总被引：1，自引：0，他引：1
海底地下水排放（SGD）是陆地向海洋输送水量和营养物质的重要通道之一,对沿海物质通量及其生物地球化学循环有重要的影响,对生态环境起着不可忽视的作用。本文运用天然放射性同位素223Ra和224Ra示踪估算了我国北方典型养殖基地桑沟湾的海底地下水排放通量。结果表明,海底地下水样尤其是间隙水中Ra活度[224Ra=（968±31）dpm/（100 L）,223Ra=（31.4±4.9）dpm/（100 L）,n=9]远高于表层海水[224Ra=（38.7±2.0）dpm/（100 L）,223Ra=（1.70±0.50）dpm/（100 L）, n=21]。假设稳态条件下,考虑Ra的各源、汇项,利用Ra平衡模型,估算出桑沟湾SGD排放通量为（0.23~1.03）×107 m3/d。潮周期内的观测结果显示,涨潮时,水力梯度较小,SGD排放变弱,落潮时,水力梯度较大,导致了相对较多的SGD排放。在一个潮周期间,基于223Ra和224Ra得到的SGD排放通量平均为0.39×107 m3/d。潮汐动力下的SGD排放平均占总SGD排放的61%,因此桑沟湾沿岸的地下水排放主要受潮汐动力的影响,并对海水组成及海陆间物质交换有显著贡献。 相似文献
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本研究调查了秋季红沿河核电站海域镭、氡同位素的活度水平及分布情况，结合镭同位素表观年龄模型计算该海域的水体年龄，进而得出研究区域的水体运移方向，初步探讨了水母丰度分布与水体运移的相关关系。得到结论如下:(1)红沿河核电站海域表层水体中224Ra、226Ra及222Rn的活度水平分别为2.9～62.4 dpm/(100 L)，11.9～57.4 dpm/(100 L)及0.1～1.3 dpm/L，镭同位素活度呈现出近岸高、远岸低的分布趋势，氡同位素的分布则更大程度上受水温控制；(2)通过224Ra/226Ra表观年龄模型计算得出红沿河海域表层水体年龄范围介于0～16 d，平均年龄(10.9±3.6) d，水体主体流向为北偏东方向，流速为7.2 cm/s；(3)水母丰度分布与水体流向呈现出较为一致的对应关系，在主体流向方向上，水体年龄较大的海域水母丰度最高。 相似文献
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海底地下水排放(SGD)是近海海域的一个重要的营养盐来源。本研究借助多种天然镭同位素对春季苏北浅滩海域的SGD及其携带入海的营养盐通量进行量化评估。研究发现:苏北浅滩海域的~(224)Ra、~(223)Ra和~(226)Ra等镭同位素的浓度水平较高,呈现近岸高、远岸低的分布趋势;根据~(224)Ra/~(226)Ra的"表观年龄模型"估算的水龄的分布情况推断,春季该海域表层水体主体流向为东北向,流速约为0.1m/s,这与前人物理海洋数值模拟结果一致;最终利用226Ra质量平衡模型发现海域的SGD通量为(46±29)cm/d,由其携带入海的溶解态无机氮、磷、硅营养盐(DIN、 DIP、 DSi)等的通量分别为(2.6±3.1)×1~09、(3.0±2.5)×10~6和(5.5±4.2)×10~8mol/d。 相似文献
5.
北黄海水体的226Ra和228Ra 总被引：1，自引：0，他引：1
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. 相似文献
6.
《应用海洋学学报》2010,(2)
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. 相似文献
7.
用HPGeγ谱分析方法测定了胶州湾表层沉积物中放射性核素含量。样品中^40K、^137Cs、^210Pb、^226Ra、^228Ra、^228Th和^238U的平均含量分别为688，3．28，61．0，26．5，40．3，44．8，39．2Bq／kg；东部海区沉积物^40K和^137Cs含量比其余海区低，但^210Pb、^226Ra、^228Ra、^228Th和^238U比其他海区高；除湾东部样品中的^210Pb、^226Ra、^228Ra、^228Th和^238U之外，粒径小于0．063mm部分中的放射性核素含量高于粒径大于0．063mm部分。除东部海区外，湾内其余海区表层沉积物中放射性核素含量和矿物组成基本一致，说明东部海区的沉积物的物质来源与其余海区不同。胶州湾表层沉积物与流域土壤放射性核素含量水平一致，所以胶州湾沉积物主要物源为流域陆源碎屑。表层沉积物中放射性核素含量与矿物组成具有相关性。铀和钍放射系衰变不平衡，总体样品和粒径小于0．063mm部分，铀系中^210Pb相对于^226Ra过剩，^226Ra相对于^238U亏损，^228Th相对于^228Ra过剩。 相似文献
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Meagan Eagle Gonneea Paul J. Morris Henrieta Dulaiova Matthew A. Charette 《Marine Chemistry》2008,109(3-4):250
Over the past decade, radium isotopes have been frequently applied as tracers of submarine groundwater discharge (SGD). The unique radium signature of SGD is acquired within the subterranean estuary, a mixing zone between fresh groundwater and seawater in coastal aquifers, yet little is known about what controls Ra cycling in this system. The focus of this study was to examine controls on sediment and groundwater radium activities within permeable aquifer sands (Waquoit Bay, MA, USA) through a combination of field and laboratory studies. In the field, a series of sediment cores and corresponding groundwater profiles were collected for analysis of the four radium isotopes, as well as dissolved and sediment associated manganese, iron, and barium. We found that in addition to greater desorption at increasing salinity, radium was also closely tied to manganese and iron redox cycling within these sediments. A series of laboratory adsorption/desorption experiments helped elucidate the importance of 1) contact time between sediment and water, 2) salinity of water in contact with sediment, 3) redox conditions of water in contact with sediment, and 4) the chemical characteristics of sediment on radium adsorption/desorption. We found that these reactions are rapid (on the order of hours), desorption increases with increasing salinity and decreasing pH, and the presence of Fe and Mn (hydr)oxides on the sediment inhibit the release of radium. These sediments have a large capacity to sorb radium from fresh water. Combined with these experimental results, we present evidence from time series groundwater sampling that within this subterranean estuary there are cyclic periods of Ra accumulation and release controlled by changing salinity and redox conditions. 相似文献
12.
226Ra and 228Ra have non-conservative excess concentrations in the mixing zones of the Pee Dee River-Winyah Bay estuary, the Yangtze River estuary, and the Delaware Bay estuary. Laboratory experiments, using Pee Dee River sediment, indicate desorption of 226Ra to increase with increasing salinities up to 20‰. In Winyah Bay desorption from river-borne sediments could contribute almost all of the increases for both isotopes. Desorption adds only a portion of the excess 228Ra measured in the Yangtse River and adjacent Shelf waters and Delaware Bay. In the Yangtze River the mixing zone extends over a considerable portion of the Continental Shelf where 228Ra is added to the water column by diffusion from bottom sediments, while 226Ra concentrations decrease from dilution. Diffusion of 228Ra from bottom sediments in Delaware Bay primarily occurs in the upper part of the bay (< 22‰ water) where fine grained sediments predominate. A diffusive flux for 228Ra of 0·33 dpm cm?2 year was determined for Delaware Bay. 相似文献
13.
226Ra and 228Ra have non-conservative excess concentrations in the mixing zones of the Pee Dee River-Winyah Bay estuary, the Yangtze River estuary, and the Delaware Bay estuary. Laboratory experiments, using Pee Dee River sediment, indicate desorption of 226Ra to increase with increasing salinities up to 20‰. In Winyah Bay desorption from river-borne sediments could contribute almost all of the increases for both isotopes. Desorption adds only a portion of the excess 228Ra measured in the Yangtse River and adjacent Shelf waters and Delaware Bay. In the Yangtze River the mixing zone extends over a considerable portion of the Continental Shelf where 228Ra is added to the water column by diffusion from bottom sediments, while 226Ra concentrations decrease from dilution. Diffusion of 228Ra from bottom sediments in Delaware Bay primarily occurs in the upper part of the bay (< 22‰ water) where fine grained sediments predominate. A diffusive flux for 228Ra of 0·33 dpm cm−2 year was determined for Delaware Bay. 相似文献
14.
Estimating submarine groundwater discharge around Isola La Cura, northern Venice Lagoon (Italy), by using the radium quartet 总被引：1，自引：0，他引：1
E. Garcia-Solsona P. Masqu J. Garcia-Orellana J. Rapaglia A.J. Beck J.K. Cochran H.J. Bokuniewicz L. Zaggia F. Collavini 《Marine Chemistry》2008,109(3-4):292
The four naturally-occurring radium isotopes (223Ra, 224Ra, 226Ra and 228Ra) were used to estimate the submarine groundwater discharge (SGD) in the Isola La Cura marsh area in the northern Venice Lagoon (Italy). By determining the radium contributors to the study area (river, coastal ocean and sediments) the radium excess in the lagoon water was quantified through a mass balance model. This radium excess is attributed to a submarine groundwater discharge source and represents the most important input of radium. Possible endmembers were considered from analysis of groundwater samples (subtidal and marsh piezometers, marsh wells and seepage meters) that were enriched in Ra by one to two orders of magnitude relative to surface waters. In particular, a permeable layer at 80 cm depth in the surrounding marsh is considered to be representative of the most likely SGD source, although similar radium activities were measured in other subtidal porewater samples collected in the Isola La Cura area. The estimated SGD flux to the study area ranged from 1 · 109 to 6 · 109 L·d− 1, the same order of magnitude as the overall riverine input to the lagoon (3 · 109 L·d− 1). A major fraction of this SGD flux is likely recirculated seawater, as evidenced by the endmember salinity. The water residence time of 2 days was estimated by both using the shortest-lived radium isotope and estimating the volume of water exchanged between the lagoon and the open sea during a tidal cycle (tidal prism approach). This SGD flux could be used to estimate the input of other chemical species (metals, nutrients, etc.) via SGD which might affect the Venice Lagoon ecosystem. 相似文献
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Patrick Ollivier Christelle Claude Olivier Radakovitch Bruno Hamelin 《Marine Chemistry》2008,109(3-4):337
Submarine groundwater discharge (SGD) is now recognized as an important pathway for water and chemical species fluxes to the coastal ocean. In order to determinate SGD to the Gulf of Lion (France), we measured the activities of 226Ra and 228Ra by thermal ionization mass spectrometry (TIMS) in coastal waters and in the deep aquifer waters of the Rhone deltaic plain after pre-concentration of radium by MnO2. Compared to conventional counting techniques, TIMS requires lower quantities of water for the analyses, and leads to higher analytical precision. Radium isotopes were thus measured on 0.25–2 L water samples containing as little as 20 fg of 226Ra and 0.2–0.4 fg of 228Ra with precision equal to 2%. We demonstrate that coastal surface waters samples are enriched in 226Ra and 228Ra compared to the samples further offshore. The high precision radium measurements display a small but significant 226Ra and 228Ra enrichment within a strip of circa 30 km from the coast. Radium activities decrease beyond this region, entrained in the northern current along the shelf break or controlled by eddy diffusion. The radium excess in the first 30 km cannot be accounted for by the river nor by the early diagenesis. The primary source of the radium enrichment must therefore be ascribed to the discharge of submarine groundwater. Using a mass-balance model, we estimated the advective fluxes of 226Ra and 228Ra through SGD to be 5.2 × 1010 and 21 × 1010 dpm/d respectively. The 226Ra activities measured in the groundwater from the Rhone deltaic plain aquifer are comparable to those from other coastal groundwater studies throughout the world. By contrast, 228Ra activities are higher by up to one order of magnitude. Taking those groundwater radium activities as typical of the submarine groundwater end-member, a minimum volume of 0.24–4.5 × 1010 l/d is required to support the excess radium isotopes on the inner shelf. This has to be compared with the average rivers water runoff of 15.4 × 1010 l/d during the study period (1.6 to 29% of the river flow). 相似文献
16.
《Marine Chemistry》2007,103(1-2):131-145
We have investigated submarine groundwater discharge to Nueces Bay (Texas) using naturally occurring Ra isotopes. Dissolved Ra activities in Nueces Bay are among the highest observed in coastal estuaries; as great as 2600 dpm m− 3 for 228Ra and 1000 dpm m− 3 for 226Ra. Using a combination of salt and Ra mass balances, we demonstrate that river discharge and bay bottom sediments cannot supply the Ra needed to balance tidal export. In the case of 226Ra there is an additional source of 218 × 106 ± 105% dpm day− 1 which is 9 times the maximum supply from bay bottom sediments and 50 times the Ra supplied by the Nueces River. A groundwater flux of 310,000 m3 day− 1 is required to supply the needed 226Ra, based on the measured maximum Ra activity of local groundwater. Though as little as 10% of this flux may be advecting terrestrial groundwater this would still represent 160% of the Nueces River discharge. This makes it unlikely that groundwater discharge alone is supplying all of the additional 226Ra. Oil-field brine could potentially account for the remainder. Leakage of 6290 m3 day− 1 of oil-field brine from the submerged petroleum wells and pipelines within the bay could supply all of the needed 226Ra. Such large fluxes of brackish groundwater and oil-field brine could significantly affect bay nitrogen budgets, salinities, and dissolved oxygen concentrations and should be considered when determining the freshwater inflow requirements for Nueces Bay and similar estuaries. 相似文献
17.
Sbastien Lamontagne Corinne Le Gal La Salle Gary J. Hancock Ian T. Webster Craig T. Simmons Andrew J. Love Julianne James-Smith Anthony J. Smith Jochen Kmpf Howard J. Fallowfield 《Marine Chemistry》2008,109(3-4):318
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. 相似文献