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51.
David W. Dyrssen 《Aquatic Geochemistry》1999,5(1):59-73
The following determinations in the Norwegian fjord Framvaren and the Black Sea have been compared: carbon-14, carbon-13, alkalinity, total dissolved inorganic carbon, sulfide, tritium (HTO), trace metals, silica, ammonium and phosphate. The historical development of the two anoxic basins is quite different. The carbon-14 age of the total inorganic dissolved carbonate in the deep water is 2000 years in the Black Sea, but only 1600 in Framvaren. The fresh water supply and composition are different. The rivers entering the Black Sea have a high alkalinity, but the river input and runoff to Framvaren has a very low alkalinity. The alkalinity, carbonate and sulfide concentrations in the anoxic waters below the chemoclines are much higher in Framvaren. This is mainly an effect of the different surface to volume ratios. The difference in carbon-13 (-8 for the Black Sea deep water, -19 in the Framvaren bottom water) is mainly due to the smaller imprint of the decomposition of organic matter on the Black Sea deep water.The concentration of trace metals in the particulate form are about the same in the deep water. About 76% of the molybdate in seawater is lost in the sulfidic water of Framvaren, and about 82–96% of the molybdate carried into the Black Sea by the Bosporus undercurrent is lost in the deep water. The relation between silica, ammonium and phosphate can be understood if part of the ammonium is being removed by denitrification, a process that most likely has been going on for thousands of years. 相似文献
52.
地下水年龄结构是了解一个地区地下水资源开采可持续性的重要基础。穆兴平原地下水开采量增加以及地下水环境恶化,对该地区可持续发展有一定制约,为此在2016年采集CFCs样品31组和3H样品60组,估算了研究区地下水年龄。结果表明,穆兴平原北部地下水年龄为21年到大于65年,由西北部和穆棱河向平原中部及乌苏里江逐渐变老,更新性变差,主要受到大气降水和地表河水补给,但是由于地表覆盖一层黏性土,地下水中缺失小于10年的水;不同井深样品中二者及NO_3~-浓度的变化,表明在60 m以上地下水的防污性能较差,而在100 m以下则较好,饮用水源井深需超过100 m。 相似文献
53.
YongHong Su Qi Feng ZongQiang Chang JianHua Si ShengKui Cao HaiYang Xi Rui Guo 《寒旱区科学》2010,2(6):0477-0492
To characterize the groundwater in the Ejina Basin,surface and groundwater samples were collected in May and October of 2002.On-site analyses included temperature,electrical conductance(EC),total alkalinity(as HCO 3) by titration,and pH.Chemical analyses were undertaken at the Geochemistry Laboratory of the Cold and Arid Region Environmental and Engineering Institute,Chinese Academy of Sciences,Lanzhou,China.The pH of the groundwater ranged from 7.18 to 8.90 with an average value of 7.72,indicating an alkaline nature.The total dissolved solids(TDS) of the groundwater ranged from 567.5 to 5,954.4 mg/L with an average of 1,543.1 mg/L and a standard deviation of 1,471.8 mg/L.According to the groundwater salinity classification of Robinove et al.(1958),47.4 percent of the samples were brackish and the remainder were fresh water.The ion concentration of the groundwater along the riverbed and near the southern margin of the basin were lower than those farther away from the riverbed.The groundwater in the study area was of Na +-HCO 3 type near the bank of the Heihe River and in the southern margin of the basin,while Na +-SO 4 2-Cl type samples were observed in the terminal lake region.In the desert area the groundwater reached a TDS of 3,000-6,000 mg/L and was predominantly by a Na +-Cl chemistry.Br/Cl for the water of Ejina Basin indicates an evaporite origin for the groundwater with a strongly depleted Br/Cl ratio(average 0.000484).The surface water was slightly enriched in Br/Cl(average 0.000711) compared with groundwater.The calculated saturation index(SI) for calcite and dolomite of the groundwater samples range from 0.89 to 1.31 and 1.67 to 2.67 with averaged 0.24 and 0.61,respectively.About 97 percent of the groundwater samples were kinetically oversaturated with respect to calcite and dolomite,and all the samples were below the equilibrium state with gypsum.Using isotope and hydrochemical analyses,this study investigated the groundwater evolution and its residence time.The groundwater content was mainly determi 相似文献
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56.
Robert L. Michel Pradeep Aggarwal Luis Araguas‐Araguas Brent D. Newman Tomas Vitvar 《水文研究》2015,29(4):572-578
Tritium concentrations in river and stream waters from different locations can be compared by normalizing them using the ratio of tritium concentrations in precipitation and surface water (Cp/Cs) in the study area. This study uses these ratios in a hydrological residence time context to make regional‐ and global‐scale comparisons about river basin dynamics. Prior to the advent of nuclear weapons testing, the Cp/Cs ratio was greater than or equal to 1 everywhere because of the decay of tritium in the watershed after it was deposited by precipitation. After an initial increase in the ratios during the bomb peak, the ratio dropped to less than 1 for most surface waters in the following years. This post‐bomb change in the ratio is due to the retention of the bomb‐pulse water in watersheds on timescales that are long relative to the residence time of tritium in the atmosphere. Ratios were calculated for over 6500 measurements of tritium in river and stream waters compiled by the International Atomic Energy Agency. These measurements span the post‐nuclear era (1940s to present) and include many long‐term datasets, which make it possible to examine residence times of waters in watersheds on a global basis. Plotting Cp/Cs versus time shows that ratios tended to reach a minimum in approximately one to two decades after the bomb peak for most locations. This result suggests that changes affecting quantity and quality of river flows need to be assessed on a multi‐decadal timescale. These long lag times have significant implications for assessing climate or land‐use change impacts on a large number of river systems around the world. The continuing value of tritium in studying surface water systems for both the Southern and Northern Hemisphere is also demonstrated. Published 2014. This article is a U.S. Government work and is in the public domain in the USA. 相似文献
57.
Tritium (3H or T) has been produced mostly by atmospheric nuclear weapon tests, and entered the ocean in the form of water (HTO). As
tritium exists as water itself, it has been regarded as an ideal tool to study the transport of water masses. In April 2001
we collected water samples in the western Japan Basin (WJB) for tritium and helium measurement. The timely sampling provided
direct evidence of the bottom water formation, resulting in the drastic increase in tritium concentration from 0.3 TU in 2000
to 0.67 TU in 2001. Considering that the new bottom waters were found mostly in the WJB, it implies that maximum 1% of the
whole bottom layer below 2600 m should be replaced with the surface water during the severely cold winter 2000—2001.3H-3He age, showing the elapsed time since the water left from the surface, can be used to calculate oxygen utilization rate by
dividing AOU by the age. Under the condition of 90% oxygen saturation in the surface water, the integration of OUR in the
water column below 200 m yields net oxygen consumption of 12 mol (O2) m-2 yr-1, which corresponds to the export production of 99 g C m-2 yr-1 . This estimate is comparable to a previous estimate based on satellite data and implies that the ratio of export to primary
production (f -ratio) is as high as 0.5 in the WJB. 相似文献
58.
Zhang Qinghua Luo Zhuanxi Lu Wen Harald Zepp Zhao Yufeng Tang Jialiang 《地理学报(英文版)》2020,30(6):935-948
Despite the increasing depletion of the groundwater at the Zhangjiakou aquifer system in the northwest of Beijing-Tianjin-Hebei region, little information is available on the hydrological process of groundwater in this region. In this study, we utilized water isotopes composition(δ~(18) O, δD and ~3 H) of groundwater, river and precipitation to identify the characteristics of hydrochemistry, groundwater age and recharge rates in different watersheds of the Zhangjiakou area. Results showed that the river water and groundwater could be characterized as HCO_3-Mg·Na, HCO_3·Cl-Na and HCO_3-Mg·Na, HCO_3·Cl-Na, HCO_3·Cl-Na·Mg types, respectively. The δD and δ~(18) O values in precipitation were linearly correlated, which is similar to the Global Meteorological Water Line(GMWL). Furthermore, the decreasing values of the δD and δ~(18) O from precipitation to surface water and groundwater indicate that groundwater is mainly recharged by atmospheric precipitation. In addition, the variation of 3 H concentration with depth suggests that groundwater shallower than around 100 m is generally modern water. In contrast, groundwater deeper around 100 m is a mixture of modern and old waters, which has longer residence times. Groundwater showed a relatively low tritium concentration in the confined aquifers, indicating the groundwater recharged might be relatively old groundwater of over 60 years. The flow velocity of the groundwater in the study area varied from 1.10 to 2.26 m/a, and the recharge rates ranged from 0.034 to 0.203 m/a. The obtained findings provide important insights into understanding the groundwater recharge sources and hydrochemistry in the Zhangjiakou area, in turn developing a sustainable groundwater management plan. 相似文献
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60.
氚作为一种天然的环境同位素可广泛应用于水文地质领域,由于实测资料的稀缺,极大地限制了氚的应用。为了能够解决这一问题,选用国际原子能机构最近发布的1960~2005年南纬50°至北纬70°区域内氚值实测资料,应用因子分析方法建立了全球大气降水中年平均氚浓度的恢复模型。选取了三个任意典型站点对采用“直接求参法”所建模型进行了验证和一个任选站点对采用“间接求参法”所建模型进行了验证,然后以南京站为例对模型进行了具体应用。因子分析应用于全球氚值恢复具有物理意义明确、适用范围广泛、操作方法简单、影响因素少,很好地恢复出氚值变化曲线的峰值和形态等特点。分析结果表明全球模型输出结果与实测值吻合,不但具有全球适用性,而且在一定程度上解决了原全球模型精度欠佳的问题,为资料稀缺和无资料地区1960~2005年大气降水中年平均氚浓度恢复提供了一种新方法。同时对模型应用中出现的问题也提出了解决方案。 相似文献