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1.
放射性核素示踪技术被广泛应用于海洋学研究。海洋沉积物是许多物质的归宿,海洋沉积过程的研究常关注3个关联问题:物质来源、沉积速率、再悬浮过程。针对这3个问题,在南海9个珊瑚礁区、北部湾涠洲岛海域、珠江口、北冰洋、南大洋等多个海区利用典型的铀系放射性核素(210Pb、226Ra、234Th、238U)示踪技术开展海洋沉积过程研究。物源识别方面,研究发现珊瑚礁区沉积物具有极低的226Ra/238U活度比值(0.1),显著低于其他海区的226Ra/238U活度比值(0.5～1.0),该独特性质可以应用于珊瑚礁区的沉积物/悬浮物来源示踪,是其他传统元素地球化学方法(Al、Ti、稀土元素)的补充。沉积速率方面,基于210Pb的恒定通量恒定沉积速率(Constant Flux Constant Sedimentation Model, CFCS)模式,定量计算了广西涠洲岛珊瑚礁区沉积柱样的沉积速率(3.7±0.6 mm/a),该结果低于中国多个近岸海域的沉积速率(5～96 mm/a)。沉积物再悬浮方面,提出利用"残余234Th"(不同于过剩234Th)示踪海洋沉积物再悬浮过程,并成功应用于北冰洋、南海、南大洋。 相似文献
2.
70年来中国化学海洋学研究的主要进展 总被引：5，自引：3，他引：2
我国的海洋化学工作者通过70年来，特别是近30年来的化学海洋学研究，实现了我国与世界先进水平进入同步发展的快车道，其显著的特点是:(1)化学海洋学研究从元素地球化学分布系统转向了以揭示深层次海洋生物地球化学过程为核心的研究；(2)化学海洋学研究实现了多领域、多视点的综合交叉研究；(3)更加关注了人为影响与自然变化共同作用下的海洋生态环境变化研究，对近海和海岸带而言，更加注重从海陆统筹一体化角度探析化学物质的分布迁移特征。本文从生源要素的海洋生物地球化学过程、微/痕量元素与同位素的海洋化学研究、生物过程作用下的化学海洋学过程等角度，重点总结归纳和分析了30年来我国海洋化学研究的重要进展和发展状况，以期对化学海洋学的进一步研究提供借鉴和启迪。 相似文献
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海洋放射年代学是同位素地质学的一门分支学科.它主要是应用天然放射性核素:230Th、231Pa、234U、238U、232Th、226Ra、210Pb、14C测定珊瑚礁、鲕岩、海泥、软体动物贝壳的年龄,测定锰结核和海洋沉积物积累的速度;研究放射性元素在海水、悬浮物和沉积物中垂直和空间分布的特征;讨论放射性元素和同位素存在形式和沉淀机理;阐述海洋物质来源;探讨锰结核成因等. 相似文献
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南极长城站附近企鹅栖息地粪土沉积地层放射性核素210Pb定年 总被引：1，自引：0，他引：1
用γ谱方法测定了南极长城站附近特有生物群落栖息地沉积物中放射性核素含量,地表沉积物中40K,137Cs,210Pb,226Ra,228Ra,228Th.和238U平均比活度,分别为143,7.56,24.1,3.65,5.36,4.15和6.5Bq/kg.同时测试了阿德雷岛企鹅栖息地粪土沉积地层中放射性核素含量,利用其中的210Pb比活度,210Pbex垂向变化特征,推演沉积物的沉积速率和地质历史年代:其中AD1-a柱样时间跨度约为74a(1928~2002年),据此计算了沉积速率为0.063mm/a(r=0.794),并讨论了在南极特定条件下,放射性核素示踪对定年影响以及与区域现代气候环境变化的内在联系. 相似文献
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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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南海东北部表层沉积物天然放射性核素与137Cs 总被引：4，自引：2，他引：4
用HPGeγ谱仪测定了南海东北部表层沉积物中的放射性核素.结果给出7种核素的平均比活度分别为40K:538Bq/kg,210Pb:116Bq/kg,226Ra:27.7Bq/kg,228Ra:4.49Bq/kg,228Th:42.0Bq/kg,238U:35.4Bq/kg和137Cs:1.16Bq/kg,210Pb的比活度随离岸距离增大,226Ra比活度随离岸距离没有明显变化,其余核素比活度随离岸距离减小.与对我国近海其他海域报道的沉积物放射性核素含量相比,40K和137Cs稍低于其他海域,其余核素为中等水平. 相似文献
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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
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钦州湾河流沉积物中镭的解吸行为 总被引：1，自引：0，他引：1
放射性镭同位素在海底地下水排放（SGD）等海洋物质变化过程的研究中具有优良的示踪作用，估算SGD通量时需要计算河流悬浮颗粒物的解吸通量。因此，对河流沉积物/悬浮颗粒物中镭同位素解吸行为的研究不可或缺，而目前对于粒度较小范围内镭同位素的解吸特征及其机理的研究依然不足。本文选用钦州湾河流沉积物，通过室内实验探究粒度和盐度对沉积物中镭同位素解吸行为的影响。结果表明，在沉积物平均粒径0.9~136.0 μm范围内，随着粒径增大，沉积物中镭同位素在海水（盐度为33.9）中解吸活度逐渐减小，且变化趋势也逐渐变缓，平均粒径大于43.7 μm后，解吸量几乎不变；在海水盐度4.9~33.9范围内，随着盐度增大，沉积物中镭同位素解吸活度逐渐增大，盐度大于24.9后，解吸量趋于不变。本文创新性地建立了沉积物表面分形结构的镭解吸理论模型，拟合得到钦州湾河流沉积物表面最大可交换态224Ra、226Ra和228Ra活度分别为1.13 dpm/g、0.17 dpm/g和0.85 dpm/g，以干重计；沉积物中224Ra、226Ra和228Ra最大解吸比分别为30%、7%和18%。钦州湾河流沉积物颗粒表面最大可交换态224Ra和226Ra活度分别处于全球中等水平和较低水平，而其最大解吸比分别处于全球较高水平和较低水平。本研究结果有助于更好地理解镭同位素的解吸行为，以帮助更准确地估算SGD通量。 相似文献
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The distributions of uranium, radium and thorium isotopes in two anoxic fjords: Framvaren Fjord (Norway) and Saanich Inlet (British Columbia) 总被引：1，自引：0，他引：1
Depth profiles of the naturally-occurring radionuclides 238U, 234U, 226Ra, 228Ra and 228Th were obtained in two diverse anoxic marine environments; the permanently anoxic Framvaren Fjord in southern Norway and the intermittently anoxic Saanich Inlet in British Columbia. Concentrations of total H2S were over three orders of magnitude greater in the anoxic bottom waters of Framvaren Fjord compared to those in Saanich Inlet.In Framvaren Fjord, the O2/H2S interface was located at 17 m. While dissolved 238U behaved conservatively throughout the oxic and anoxic water columns, concentrations based on the 238U/salinity ratio in oxic oceanic waters were almost 30% lower. Dissolved 226Ra displayed a sharp maximum just below the O2/H2S interface, coinciding with dissolved Mn (II) and Fe (II) maxima in this zone. It is suggested that reductive dissolution of Fe-Mn oxyhydroxides remobilizes 226Ra in this region.In Saanich Inlet, the O2/H2S interface was located at 175 m. Dissolved 238U displayed a strongly nonconservative distribution. The depth profiles of dissolved 226Ra and 228Th correlated well with the distribution of dissolved Mn (II) in the suboxic waters above the O2/H2S interface, suggesting that reduction of particulate Mn regulates the behavior of 226Ra and 228Th in this region.Removal residence times for dissolved 228Th in the surface oxic waters of both systems are longer than those generally reported for particle-reactive radionuclides in coastal marine environments. In the anoxic waters of Framvaren Fjord and Saanich Inlet, however, the dissolved 228Th removal residence times are quite similar to values reported for dissolved 210Pb in the anoxic waters of the Cariaco Trench and the Orca Basin. This implies that the geochemistries of Th and Pb may be similar in anoxic marine waters. 相似文献
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U–Th decay series isotopes, δ18O and Si measurements in the river estuarine waters and sediments of the polluted Hooghly estuary as well as the surface waters of the Bay of Bengal, its high salinity end member, are reported. Dissolved Si indicates that there are probably two mixing regimes, dissolved U behaviour is nonconservative and δ18O behaves conservatively in the overall estuarine region. Isotopes of reactive elements, viz. 234Th and 210Po, are removed from the estuarine waters in <2 days and <1 month, respectively, which is due to high suspended matter (30–301 mg l−1). 228Ra and 226Ra are profusely released into the estuarine waters in the low to mid-salinity regions.As expected, the opposite trend is observed in the case of estuarine sediments and suspended matter. Reactive isotopes of Th, 210Pb and 210Po are enriched, whereas Ra isotopes are depleted with respect to their parent nuclides in the estuarine sediments and suspended matter. 232Th/Al ratio appears well suited to study the distribution and mixing of the bed load sediments of the Ganga–Brahmaputra (G–B) and the Hooghly rivers with those from other rivers on the Bay of Bengal floor. 相似文献
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The concentration of thorium isotopes and the activity ratios of230Th/232Th and228Th/232Th in sea water collected in the Kuroshio region, the mixing area of Oyashio and Kuroshio, the Japan Sea and the East China
Sea in the western North Pacific were determined. Thorium isotopes were analyzed by α-ray spectrometry after separating them
with an anion exchange resin. The average content of thorium (232Th) of 2.2×10−9 g/l was obtained in the open Pacific waters. The ratio of230Th/232Th is in accord with that of the top layer of the sediment in the same area. The high values of228Th/232Th ratio up to 36 were observed in sea water. The excess228Th in sea water may be due to the migration of228Ra through the water-sediment interface. Thorium content in suspended matter was 10 to 20% of the total thorium content in
the Pacific water. 相似文献
14.
铜(Cu)是海洋浮游植物生长不可或缺的痕量金属之一, 对海洋初级生产力起着关键作用。河流是海洋中Cu的重要来源, 河口及边缘海对河流输入的Cu起着重要的改造作用, 但目前对Cu在浙闽沿岸的生物地球化学行为尚不明确。本研究使用自动固相萃取-电感耦合等离子体联用技术对2021年11月浙闽沿岸及其邻近水域表层水的溶解态铜(dCu)浓度进行分析。结果显示，该区域dCu浓度范围为3.38~26.28 nmol·L-1, 平均浓度为11.66±5.83 nmol·L-1。在研究区域内, dCu的空间分布呈北高南低, 近岸高、远岸低的特征。此外, dCu在浙闽沿岸表现出较高的保守性, 其与盐度呈显著负相关关系, 表明dCu在一定程度上可用于指示人为影响。相关性分析表明, 浙闽沿岸及其邻近水域表层dCu的生物地球化学行为和分布可能受到陆源输入、水团输运混合、化学絮凝与吸附等过程的影响。本研究结果有助于进一步理解Cu在海洋中的生物地球化学过程, 为探究该区域的生态环境变化提供科学依据。 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
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In the current study, low-background γ-spectrometry was employed to determine the 228Ra/226Ra activity ratio and 137Cs activity of 84 coastal water samples collected at six sites along the main island of Japan (Honshu Island) within the Sea of Japan, including the Tsushima Strait, and two other representative sites on Honshu Island (a Pacific shore and the Tsugaru Strait) at 1-month intervals in 2006.The 228Ra/226Ra ratio of coastal waters in the Sea of Japan exhibited similar patterns of seasonal variation, with minimum values during early summer (228Ra/226Ra = 0.6–0.8), maximum values during autumn (228Ra/226Ra = 1.5–3), and a time lag in their temporal changes ( 2.5 months and over 1300 km distance). However, the 2 other sites represented no clear periodic variation.In contrast to the positive correlation between 137Cs activity (0.6–1.7 mBq/L) and salinity (15–35), the 228Ra/226Ra ratio of coastal water samples from the Sea of Japan was not observed to correlate with salinity, and the increase in the 228Ra/226Ra ratio was not as marked (0.5–1; May–June 2004 and 2005) during the migration along Honshu Island. The input of land-derived water and/or the diffusion of radium from coastal sediments is unlikely to have affected the wide seasonal variation in the 228Ra/226Ra ratio observed in these water samples.The seasonal variation in the 228Ra/226Ra ratio recorded for the coastal waters of the Sea of Japan is considered to be mainly controlled by the remarkable changes in the mixing ratio of the 228Ra-poor Kuroshio and the 228Ra-rich continental shelf waters within the East China Sea (ECS). After passing through the Tsushima Strait, this water mass moves northeast along the coastline of the Sea of Japan as the Tsushima Coastal Branch Current (TCBC). 相似文献