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1.
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   

2.
《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   

3.
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   

4.
There is increasing evidence that submarine groundwater discharge (SGD) in many areas represents a major source of dissolved chemical constituents to the coastal ocean. In Great South Bay, NY, previous studies have shown that the discharge of nutrients with SGD may cause harmful algal blooms. This study estimates SGD to Great South Bay during August 2006 by performing a mass balance for each of the dissolved Ra isotopes (224Ra, 223Ra, 228Ra, 226Ra). The budget indicates a major unknown source (between 30 and 60% of the total input) of Ra to the bay. This imbalance can be resolved by a flux of Ra-enriched groundwater on the order of 3.5–4.5 × 109 L d− 1, depending on the Ra isotope. The Ra-estimated SGD rates compare well with those previously estimated by models of flow that decreases exponentially away from shore. Compared to previous reports of fresh groundwater discharge to the bay, the Ra-estimated discharge must comprise approximately 90% recirculated seawater. The good agreement between Ra- and model-estimated flow rates indicates that the primary SGD endmember may be best sampled at shallow depths in the sediments a short distance bayward of the low tide line.  相似文献   

5.
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   

6.
A mass balance for the naturally-occurring radium isotopes (224Ra, 223Ra, 228Ra, and 226Ra) in Jamaica Bay, NY, was conducted by directly estimating the individual Ra contributions of wastewater discharge, diffusion from fine-grained subtidal sediments, water percolation through marshes, desorption from resuspended particles, and water exchange at the inlet. The mass balance revealed a major unknown source term accounting for 19–71% of the total Ra input, which could only be resolved by invoking a source from submarine groundwater. Shallow (< 2 m depth) groundwater from permeable sediments in Jamaica Bay was brackish and enriched in Ra relative to surface bay waters by over two orders of magnitude. To balance Ra fluxes, a submarine groundwater input of 0.8 × 109–9.0 × 109 L d− 1 was required. This flux was similar for all four isotopes, with individual estimates varying by less than a factor of 2. Our calculated groundwater flux was 6- to 70-fold higher than the fresh groundwater discharge to the bay estimated by hydrological methods, but closely matched direct flow rates measured with seepage meters. This suggests that a substantial portion of the discharge consisted of recirculated seawater. The magnitude of submarine groundwater discharge varied seasonally, in the order: summer > autumn > spring. Chemical analyses suggest that the recirculated seawater component of submarine groundwater delivers as much dissolved nitrogen to the bay as the fresh groundwater flux.  相似文献   

7.
北黄海水体的226Ra和228Ra   总被引：1，自引：0，他引：1  
王芬芬  门武  刘广山 《台湾海峡》2010,29(2):265-276
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   

8.
A total of 21 surface water samples were collected on the east side of the East China Sea (ECS) (3 sites) and at the Tsushima Strait (1 site), and 226Ra and 228Ra activities were measured using low-background γ-spectrometry. The 228Ra/226Ra ratios among the samples exhibited notable seasonal variation (228Ra/226Ra = 0.2–2.6) accompanying changes of salinity (31.7–34.7). Seasonal water circulation within the ECS is hypothesized to cause the change by altering the mixing ratio of 228Ra-rich continental shelf water and 228Ra-poor Kuroshio water.  相似文献   

9.
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   

10.
Activities of the naturally occurring radium nuclides 228Ra, 226Ra, 224Ra and 223Ra were determined in waters of the open German Bight and adjacent nearshore areas in the North Sea, in order to explore the potential use of radium isotopes as natural tracers of land–ocean interaction in an environment characterised by extensive tidal flats, as well as riverine and groundwater influx. Data collected at various tidal phases from the Weser Estuary (228Ra: 46.3 ± 4.6; 226Ra: 17.1 ± 1.1; 224Ra: 26.1 ± 8.2 to 36.5 ± 6.1; 223Ra: 1.8 ± 0.1 to 4.0 ± 0.4), tidal flats near Sahlenburg (228Ra: 39.3 ± 3.8 to 46.0 ± 4.5; 226Ra: 15.5 ± 1.5 to 16.5 ± 1.7; 224Ra: 34.3 ± 2.2 to 85.3 ± 6.3; 223Ra: 3.6 ± 0.5 to 8.0 ± 1.2), freshwater seeps on tidal flats near Sahlenburg (228Ra: 42.1 ± 4.1; 226Ra: 21.3 ± 2.2; 224Ra: 5.1 ± 0.9; 223Ra: 2.6 ± 1.3) and also in permanently inundated parts of the North Sea (228Ra: 23.0 ± 2.3 to 28.2 ± 2.8; 226Ra: 8.2 ± 0.8 to 11.8 ± 1.2; 224Ra: 3.1 ± 1.0 to 10.1 ± 0.9; 223Ra: 0.1 ± 0.02 to 0.9 ± 0.05; units: disintegrations per minute per 100 kg water sample) reveal that, except for the fresh groundwater, the potential end-members of nearshore water mass mixing have quite similar radium signatures, excluding a simple discrimination between the sources. However, the decreasing activities of the short-lived 224Ra and 223Ra isotopes recorded towards the island of Helgoland in the central German Bight show a potential to constrain fluxes of land-derived material to the open North Sea. The largest source for all radium isotopes is generally found on the vast tidal flats and in the Weser Estuary. Future work could meaningfully combine this so-called radium quartet approach with investigations of radon activity. Indeed, preliminary data from a tidal flat site with fresh groundwater seepage reveal a 222Rn signal that is clearly lower in seawater.  相似文献   

11.
The distribution of trace metals in sediments and their exchange between sediments and overlying water is governed by multiple processes including molecular diffusion, bioturbation (porewater advection, porewater mixing, and particle mixing), chemical reactions and adsorption–desorption. To understand these processes and their relative contributions, a one-dimensional model was built, which includes bioturbation and adsorption–desorption processes, to describe the transport of 224Ra. Because 224Ra is adsorbed on MnO2, 224Ra may serve as a proxy for trace metal transport. Three sites were sampled and both dissolved and adsorbed 224Ra were analyzed and modeled to understand the transport and exchange processes. It was found that particle transport of adsorbed 224Ra followed by desorption at the sediment/water interface typically represents the dominant flux. We have further been able to define conditions where the porewater transport for adsorption reactive metals like 224Ra (and other metals) may be out of the sediments whereas the active scavenging of 224Ra from the water column at the sediment water interface via adsorption reactions can result in a flux of 224Ra into the sediment. These processes are both predicted by the model and observed in sediment samples.  相似文献   

12.
The concentrations of228Ra in surface waters of the Seto Inland Sea were determined. Surface waters from the central region of the Seto Inland Sea, Hiuchi Nada and Bingo Nada, contained concentrations of228Ra of 655–811 dpm/1000 l which were 100 times higher than those obtained in the Pacific Ocean. These high concentrations of228Ra must be supported by a228Ra flux from the bottom sediment. The lower limit of this flux was estimated to be more than 0.16 dpm cm–2 y–1. The228Ra concentrations decreased markedly from central regions of the Seto Inland Sea to about 18 dpm/1000 l in the Kii and the Bungo Channels as salinity increased. Using a box model and the228Ra data, the mean residence time of sea water in the Seto Inland Sea with respect to the exchange with the open ocean water was estimated to be less than 10 y, and the most probable value is the order of several years.  相似文献   

13.
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   

14.
Activities of the natural radionuclides 226Ra (T1/2 =1602 years) and 22sRa (T1/2 =5.75 years) in particulate matter are reported from sediment traps deployed in the tropical northeast Atlantic. 228Ra/226Ra activity ratios in settling particles are compared to those found in the water column in order to specify the origin of radium incorporated in particulate matter, and consequently that of barium, since the two elements are known to display close geochemical behaviours in the oceans. Whereas 228Ra/226Ra activity ratios in the water column display very large variations with depth, they remain nearly constant in particles, with values close to those found in the upper 250 m. These results clearly demonstrate that particles acquire their radium and, by inference, their barium, in the upper water column and that there is very little exchange with the dissolved phase as they settle to the bottom.  相似文献   

15.
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   

16.
Submarine groundwater discharge (SGD) to coastal southern Rhode Island was estimated from measurements of the naturally-occurring radioisotopes 226Ra (t1/2 = 1600 y) and 228Ra (t1/2 = 5.75 y). Surface water and porewater samples were collected quarterly in Winnapaug, Quonochontaug, Ninigret, Green Hill, and Pt. Judith–Potter Ponds, as well as nearly monthly in the surface water of Rhode Island Sound, from January 2002 to August 2003; additional porewater samples were collected in August 2005. Surface water activities ranged from 12–83 dpm 100 L− 1 (60 dpm = 1 Bq) and 21–256 dpm 100 L− 1 for 226Ra and 228Ra, respectively. Porewater 226Ra activities ranged from 16–736 dpm 100 L− 1 (2002–2003) and 95–815 dpm 100 L− 1 (2005), while porewater 228Ra activities ranged from 23–1265 dpm 100 L− 1. Combining these data with a simple box model provided average 226Ra-based submarine groundwater fluxes ranging from 11–159 L m− 2 d− 1 and average 228Ra-derived fluxes of 15–259 L m− 2 d− 1. Seasonal changes in Ra-derived SGD were apparent in all ponds as well as between ponds, with SGD values of 30–472 L m− 2 d− 1 (Winnapaug Pond), 6–20 L m− 2 d− 1 (Quonochontaug Pond), 36–273 L m− 2 d− 1 (Ninigret Pond), 29–76 L m− 2 d− 1 (Green Hill Pond), and 19–83 L m− 2 d− 1 (Pt. Judith–Potter Pond). These Ra-derived fluxes are up to two orders of magnitude higher than results predicted by a numerical model of groundwater flow, estimates of aquifer recharge for the study period, and values published in previous Ra-based SGD studies in Rhode Island. This disparity may result from differences in the type of flow (recirculated seawater versus fresh groundwater) determined using each technique, as well as variability in porewater Ra activity.  相似文献   

17.
The distributions of dissolved organic carbon (DOC), Ba, U, and a suite of naturally occurring radionuclides in the U/Th decay series (222Rn, 223,224,226,228Ra) were studied during high- and low-discharge conditions in the Loxahatchee River estuary, Florida to examine the role of submarine groundwater discharge in estuarine transport. The fresh water endmember of this still relatively pristine estuary may reflect not only river-borne constituents, but also those advected during active groundwater/surface water (hyporheic) exchange. During both discharge conditions, Ba concentrations indicated slight non-conservative mixing. Such Ba excesses could be attributed either to submarine groundwater discharge or particle desorption processes. Estuarine dissolved organic carbon concentrations were highest at salinities closest to zero. Uranium distributions were lowest in the fresh water sites and mixed mostly conservatively with an increase in salinity. Suspended particulate matter (SPM) concentrations were generally lowest (< 5 mg L− 1) close to zero salinity and increased several-fold ( 18 mg L− 1; low discharge) toward the seaward endmember, which may be attributed to dynamic resuspension of bottom sediments within Jupiter Inlet.Surface water-column 222Rn activities were most elevated (> 28 dpm L− 1) at the freshwater endmember of the estuary and appear to identify regions of the river most influenced by the discharge of fresh groundwater. Activities of four naturally occurring isotopes of Ra (223,224,226,228Ra) in this estuary and select adjacent shallow groundwater wells yield mean estuarine water-mass transit times of less than 1 day; these values are in close agreement to those calculated by tidal prism and tidal frequency. Submarine groundwater discharge rates to the Loxahatchee River estuary were calculated using a tidal prism approach, an excess 226Ra mass balance, and an electromagnetic seepage meter. Average SGD rates ranged from 1.0 to 3.8 × 105 m3 d− 1 (20–74 L m− 2 d− 1), depending on river-discharge stage. Such calculated SGD estimates, which must include both a recirculated as well as fresh water component, are in close agreement with results obtained from a first-order watershed mass balance. Average submarine groundwater discharge rates yield NH4+ and PO4− 3 flux estimates to the Loxahatchee River estuary that range from 62.7 to 1063.1 and 69.2 to 378.5 μmol m− 2 d− 1, respectively, depending on river stage. SGD-derived nutrient flux rates are compared to yearly computed riverine total N and total P load estimates.  相似文献   

18.
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.  相似文献   

19.
Using manganese-impregnated fiber extraction and high-efficiency gamma counting techniques, we measured the distribution of 228Ra and 226Ra in surface waters near the coast of Japan and in the western North Pacific. There is no evidence in our data that any significant amount of 228Ra is added to open ocean surface waters from the coastal waters around Tokyo Bay. High 228Ra concentrations (> 10 dpm/103 kg), were observed along the Kuroshio Current as compared to < 2.5 dpm/103 kg between 10° and 30°N of the central gyre, and hence the major source of 228Ra in the surface water is likely to be the East Asian continental shelf zones. A simple one-dimensional eddy diffusion and advection model is used to explain the observed decrease of 228Ra from coast to the open ocean. The model results indicate two mixing regimes across the Kuroshio Current System with apparent eddy diffusion coefficients of Ky = 4 × 105 cm2 s−1 at distance y < 200 km from the coast, and Ky = 4 × 107 cm2 s−1 at y > 200 km. Along 40°N where an eastward flow of the ‘Kuroshio Extension’ prevails, an advective flow of > 0.1 knot is consistent with the observation of nearly constant 228Ra along the track.The geographical distribution pattern of 228Ra is clearly different from that of atmospherically derived 210Pb. Thus the 228Ra in surface water serves as a useful tracer that accompanies fluvially and coastally derived elements during their subsequent lateral transport toward the central gyre.  相似文献   

20.
白令海峡水团来源的镭同位素示踪   总被引：4，自引：3，他引：1       下载免费PDF全文
对白令海峡64.3°N纬向断面镭同位素的研究表明,水体中226Ra比活度、228Ra比活度和228Ra/226Ra)A.R.存在明显的纬向变化,反映出太平洋与北冰洋水体交换的多种路径.根据温度、盐度和镭同位素的水平与垂直分布,太平洋水进入北冰洋的路径可能主要有3支,分别为白令海峡西侧的阿拉德水、白令海峡东侧的阿拉斯加沿...  相似文献   

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