The analysis of nitrate in highly saline waters

The analysis of nitrate in seawater and hypersaline waters should take account of a significant “salt effect”. Procedures developed for fresh water and marine waters must be applied cautiously to highly saline waters. The most widely used standard method for the determination of nitrate-nitrogen (NO₃-N) in fresh and marine waters involves the quantitative reduction of nitrate by the Cd column technique followed by colorimetric procedures. In our study, three approaches to estimate NO₃-N in highly saline waters were examined. The first involved dilution. This approach overcame the salt effect but dilution limited the detection of low concentrations of nitrate in highly saline waters. The second involved the use of standard nitrate solutions in saline water. This method is not recommended because of nitrate impurities in AR grade salts. The third- and preferred approach-involved the use of standard additions. “Spikes” of a known volume of NO₃-N standard solution were added to natural saline waters. Nitrate values estimated by the stadard addition method were used to calculate an equation for salt error correction at different salinities applicable to waters with the same relative ionic composition as seawater. This could then be used to correct nitrate determinations in highly saline waters where standards made in distilled water were used for calibration. Many previously published data for NO₃-N in saline water used methods of analysis which do not take account of salt error and are therefore probably in error.     

赣江上游河流水化学的影响因素及DIC来源

对赣江上游38 处水体采样点的水化学特征和溶解无机碳稳定同位素的分析, 发现其总溶解质浓度较低, 其中, 阳离子以Na⁺、Ca²⁺ 为主, 阴离子以Cl^- 和HCO₃ ^- 为主, Si 的浓度较高, 表征了典型硅酸盐地区河流的水化学组成特征。通过海盐校正分析得出, 研究区大气降水对河水溶解质的贡献率为11.5%, 扣除降水的贡献部分, 利用主成分分析的方法, 计算得出赣南流域受硅酸盐岩风化作用强烈, 同时由于受附近盐矿的影响, 蒸发盐岩的风化作用显著。另外, 根据δ¹³C 溶解无机碳DIC 的测量值约为-8.35‰~-13.74‰, 平均为-11.65‰, 利用质量平衡计算得出, 研究区DIC 的主要来源, 约68.5%来自于土壤CO₂, 31.5%来自于碳酸盐矿物的溶解, 进而得出流域岩石化学风化过程消耗的土壤CO₂ 为2.11×105 mol/yr·km², 来自碳酸盐本身的HCO₃ ^-含量为9.6×104 mol/yr·km²。由于地理位置和流域环境以及人为因素的差异, 各支流DIC 来源的比例亦有所差异。     

Geochemistry of waters and brines from the Salinas Grandes basin,Córdoba,Argentina. II. Gypsum dissolution-calcite precipitation,and brine evolution

Rivers and streams originating in the surrounding mountainous area are the major sources of salt in the Salinas Grandes basin (Córdoba, Argentina). These rivers infiltrate when they reach the sandflat or in the fringes of the mudflat, feeding springs which often form shallow lakes. Presently, the lakes are distant from the playa edge, thus allowing inflow waters to dissolve ancient (Pleistocene?) evaporite beds. In the sandflat environment, two dominant types of water have been recognized (SO ₄ ^2? -Cl^?-HCO ₃ ^? -Na⁺, and Cl^?-SO ₄ ^2? -HCO ₃ ^2? -Na⁺), both considered as original members of the brine in the saline complex. Two main sources of solutes were distinguished, one related to the waters supplied by the southern sector and another to waters of the eastern sector. As a result of the chemical evolution in the playa environment, all brines belong to the neutral type (Cl^?-SO ₄ ^2? -Na⁺). Following Hardie and Eugster's (1970) model, waters from the southern sector should evolve towards an alkaline brine (Cl^?-SO ₄ ^2? -HCO ₃ ^? -Na⁺), whereas those from to the eastern sector should evolve towards a neutral one (Cl^?-SO ₄ ^2? -Na⁺). A computer simulation was carried out to model the chemical evolution of source waters. The results obtained by this methodology showed the same dichotomy (alkaline vs. neutral) established by Hardie and Eugster's (1970) model. The deficit in alkalinity could not be explained by any of the mechanisms published until now. Gypsum dissolution is the most likely mechanism which accounts for the chemical evolution of the waters investigated. When such a process is included in the computations, the Ca²⁺ supplied by gypsum beds generates an increase in the ion activity product (aCa⁺²·aCO ₃ ^2? ) and produces a significant change in the 2Ca⁺²/(2CO ₃ ^2? +HCO ₃ ^? ) ratio, switching from values less than 1 to values greater than 1. This process determines the precipitation of calcite, and leads to a decrease in alkalinity, which in turn would explain the existence of a neutral brine in the saline complex. An intermediate salinity brine was detected in the mudflat, which, according to the model (Hardie and Eugster, 1970), should evolve towards a SO ₄ ^2? -free neutral brine (Cl^?-Na⁺-Ca²⁺). The absence of this type of brine may be explained through mixing processes.     

Chemical composition of glacial meltwaters and river waters within the Aktru river basin (Gornyi Altai)

An assessment was made of the mean levels of major and trace elements and of biogenic and organic matter in glacial and river waters within the Aktru river basin (Gornyi Altai, Russia). The analysis showed a general tendency for an increase in mineralization along the direction from the region of alimentation of glaciers to the mouth of the river. A relatively abrupt increase was revealed in Al, Zn, Cu, Pb, Si, NO₂ ^? and NH₄ ⁺ concentrations in the source of the Aktru river and its glacial tributaries, with their subsequent decrease downstream. The mechanism for such changes is governed by the conditions of interaction of rocks with meltwaters and river waters.     

Assessing the Influence of the Mining Operations on the State of Streams in the Northern Part of the Red River Basin (Viet Nam)

A study was made of the influence of extraction of lead and zinc ores in the northern part of Vietnam (the Red river basin, Chodon district of Bac Can Province, and the basins of the Dai, Ban Thi, Ta Dieng and Cau rivers). Background concentrations of macro- and microelements and biogenic elements are determined in the river waters and water extracts from bottom sediments of small streams of the study area. A significance exceedance of background concentrations was revealed in stretches of the headwaters of the Ban Thi and Dai rivers caused by a combination of natural and anthropogenic factors. It is established that the river waters near the pollution sources contain increased (compared with the geochemical background) concentrations of Zn, Pb, Fe, Ni, Co, As, Bi, Cd, Cs, Sb, Ag,NO₂^? and SO₄^2?. The waters are estimated as moderately and heavily polluted, and at the other points as minimally polluted. It is determined that the level of accumulation of matter in water extracts from bottom sediments with respect to the geochemical background in the vicinity of the ore dressing factories corresponds to weakly and heavily polluted bottom sediments, and further downstream, to thy minimum level of pollution. It is shown that the influence of extraction of lead and zinc ores on the state of small streams is observed in stretches as long as 11–12 km (with a maximum in stretches of up to 4.5 km). The mathematical model of Pb and Zn distribution in the river waters of the study area has been developed and tested.     

Cost Implications of Uncertainty in CO<Subscript>2</Subscript> Storage Resource Estimates: A Review

Carbon capture from stationary sources and geologic storage of carbon dioxide (CO₂) is an important option to include in strategies to mitigate greenhouse gas emissions. However, the potential costs of commercial-scale CO₂ storage are not well constrained, stemming from the inherent uncertainty in storage resource estimates coupled with a lack of detailed estimates of the infrastructure needed to access those resources. Storage resource estimates are highly dependent on storage efficiency values or storage coefficients, which are calculated based on ranges of uncertain geological and physical reservoir parameters. If dynamic factors (such as variability in storage efficiencies, pressure interference, and acceptable injection rates over time), reservoir pressure limitations, boundaries on migration of CO₂, consideration of closed or semi-closed saline reservoir systems, and other possible constraints on the technically accessible CO₂ storage resource (TASR) are accounted for, it is likely that only a fraction of the TASR could be available without incurring significant additional costs. Although storage resource estimates typically assume that any issues with pressure buildup due to CO₂ injection will be mitigated by reservoir pressure management, estimates of the costs of CO₂ storage generally do not include the costs of active pressure management. Production of saline waters (brines) could be essential to increasing the dynamic storage capacity of most reservoirs, but including the costs of this critical method of reservoir pressure management could increase current estimates of the costs of CO₂ storage by two times, or more. Even without considering the implications for reservoir pressure management, geologic uncertainty can significantly impact CO₂ storage capacities and costs, and contribute to uncertainty in carbon capture and storage (CCS) systems. Given the current state of available information and the scarcity of (data from) long-term commercial-scale CO₂ storage projects, decision makers may experience considerable difficulty in ascertaining the realistic potential, the likely costs, and the most beneficial pattern of deployment of CCS as an option to reduce CO₂ concentrations in the atmosphere.     

塔里木河中下游地下水化学及其演变特征分析

 通过对塔里木河中下游14个断面57眼地下水监测井样品离子化学成分分析,探讨了塔里木河中下游地下水化学成分特点、水化学类型及演化规律。结果表明：塔里木河中下游各断面地下水pH值变化不大,矿化度和各离子差异明显,地下水水样以Na⁺、Cl^-占绝对优势;矿化度较低的断面其离子浓度变化较小,反之,矿化度高的断面其离子浓度变化幅度较大;从塔里木河中游沙吉利克断面至铁依孜断面地下水化学类型由以Cl-SO₄-Na、Cl-Na-Mg和Cl-SO₄-Na-Mg型水为主,逐渐过渡为以Cl-SO₄-Na-Mg和Cl-Na型水为主,在下游阿克敦断面至考干断面地下水化学类型由以Cl-SO₄-Na-Mg、Cl-Na-Mg型水为主过渡为以Cl-Na、Cl-HCO₃-Na和Cl-Na-Mg为主;时间上,2006年中游断面沿河道地下水化学类型由Cl-SO₄-HCO₃-Na型过渡为Cl-SO₄-Na-Mg型再到Cl-Na型水,而2010年则由Cl-SO₄-Na型过渡为Cl-SO₄-Na-Mg型再到Cl-Na型水,在下游,2006年沿河道地下水化学类型由Cl-SO₄-Na型过渡为Cl-SO₄-Na-Mg型再到Cl-Na（Mg）型水,2010年则由Cl-SO₄-Na-Mg型直接过渡为Cl-Na-Mg型和Cl-Na型水。塔里木河中下游水样化学组成均落在Gibbs提出的Boomerang Envelope模型上翼,暗示研究区水样化学组成受到蒸发/结晶作用影响。另外,土地利用变化、灌溉、施肥等人为活动的影响不容忽视。     

Effects of heavy metals on the survival ofDiacypris compacta (Herbst) (Ostracoda) from the Coorong,South Australia

The hypermarine southern Coorong is threatened by proposals to drain relatively fresh surface water and groundwater from adjacent agricultural areas into the Coorong. These influent waters carry moderate loads of heavy metals. Acute toxicity of heavy metals toDiacypris compacta, an abundant ostracod in the Coorong, was measured in the laboratory at 18°C in a static system using Coorong water (pH 7.8 salinity 50 ppt). At 4 days (96 h) the mean values of LC₅₀ for copper, zinc, lead and, cadmium respectively were 0.8, 2.1, 3.1 and 4.3 mg L^–1, and at 8 days the respective mean LC₅₀ s were 0.4, 0.7, 2.2 and 1.1 mgL^–1. The effect of two or three metals on mortality was additive in some cases and synergistic in other cases, but generally less than additive. However, in all cases mortality was greater in the presence of two or three metals than in the presence of a single metal. According to ANZECC (1992) guidelines, maximum acceptable concentrations of heavy metals should be no higher than 0.01 x the lowest LC₅₀ value. Using the lowest LC₅₀ values forDiacypris compacta obtained at 8 days, maximum acceptable concentrations in the Coorong would be 4, 5, 9 and 22 gL^–1 for copper, zinc, cadmium and lead respectively, the values for zinc and copper failling below those recommended by ANZECC (1992) for marine waters. Reported concentrations of copper and zinc in surface water and groundwater in areas adjacent to the Coorong sometimes exceed these values, hence drainage of these waters into the Coorong represents a significant hazard to the Coorong biota.     

Arctic freshwater ostracods from modern periglacial environments in the Lena River Delta (Siberian Arctic,Russia): geochemical applications for palaeoenvironmental reconstructions

The aim of this study is to describe ostracods from freshwater habitats in the Siberian Arctic in order to estimate the present-day relationships between the environmental setting and the geochemical properties of ostracod calcite. A special focus is on the element ratios (Mg/Ca, Sr/Ca), and the stable isotope composition (δ¹⁸O, δ¹³C), in both ambient waters and ostracod calcite. The most common species are Fabaeformiscandona pedata and F. harmsworthi with the highest frequency in all studied waters. Average partition coefficients D(Sr) of F. pedata are 0.33 ± 0.06 (1σ) in females, and 0.32 ± 0.06 (1σ) in males. A near 1:1 relationship of δ¹⁸O was found, with a mean shift of Δ_mean = 2.2‰ ± 0.5 (1σ) to heavier values in ostracod calcite of F. pedata as compared to ambient waters. The shift is not dependent on δ¹⁸O_water, and is caused by metabolic (vital) and temperature effects. Temperature-dependence is reflected in the variations of this shift. For ostracod calcite of F. pedata a vital effect as compared to inorganic calcite in equilibrium was quantified with 1.4‰. Results of this study are valuable for the palaeoenvironmental interpretation of geochemical data of fossil ostracods from permafrost deposits.     

非点源污染研究中土壤溶解性无机氮的提取方法选择

用2M KCl溶液(5:1)、饱和CaSO4溶液(5:1)、0.01M CaCl₂溶液(20:1,100:1) 和去离子水(20:1,100:1)4种提取液、6种提取方式,采用Auto-analyzerⅢColorimeter (Bran Luebbe),水杨酸-次氯酸盐法和Griess-Ilosvay法测定并对比了北京地区4种天然土样的溶解性氨氮和硝态氮的含量。研究结果表明:溶解性硝态氮的测定结果不受提取液和水土比(小于100:1)的影响,而溶解性氨氮测定结果受影响较大。在非点源污染研究中,对于土壤中可向水体迁移的溶解性无机氮含量的测定,应根据来水水源特征和研究目的选择适宜的浸提剂和水土比。     

Hydrochemical regime and its mechanism in Yamzhog Yumco Basin,South Tibet

The hydrochemistry of alpine lakes reflects water characteristic and its response to climatic change. Over 300 water samples had been collected from 52 sites of 5 lakes and 7 inflowing rivers in the Yamzhog Yumco Basin, South Tibet, during 2009–2014, basing which the hydrochemical regime and its mechanism were analyzed along with the adoption of hydrological investigations in 1979 and 1984 as well. Results revealed that the waters were hard with weak alkalinity for the Yamzhog Yumco Basin. Most of them were fresh, and the rest were slightly saline. The hydrochemical types of 5 lakes (i.e., Lake Yamzhog Yum Co, Puma Yum Co, Bajiu Co, Kongmu Co, and Chen Co) were SO₄ ^2––HCO₃ ^––Mg²⁺–Na⁺, HCO₃ ^––SO₄ ^2––Mg²⁺–Ca²⁺, SO₄ ^2––Mg²⁺–Na⁺, SO₄ ^2––HCO₃ ^––Ca²⁺, and SO₄ ^2––Na⁺–Mg²⁺–Ca²⁺, respectively. As for rivers, HCO₃ ^– and SO₄ ^2– were the major anions, and Ca²⁺ was the dominant cation. Lake Yamzhog Yum Co, the largest lake in the basin, exhibited remarkable spatial variations in hydrochemistry at its surface but irregular changes with depth. The weathering of evaporates and carbonates, together with evaporation and crystallization, were the major mechanisms controlling the hydrochemistry of waters in the Yamzhog Yumco Basin. Global warming also had significant impacts on hydrochemical variations.     

SEASONAL INORGANIC NITROGEN RELEASE IN ALPINE LAKES ON THE COLORADO WESTERN SLOPE

In the Rocky Mountains, the association of increases in acidic deposition with increased atmospheric loading of sulfate and direct changes in surface water chemistry has been well established. The importance, though, of increased nitrogen (N) deposition in the episodic acidification of alpine lakes and N saturation in alpine ecosystems is only beginning to be documented. In alpine areas of the Colorado Front Range, modest loadings of N in deposition have been associated with leakage of N to surface waters. On the Colorado western slope, however, no leakage of N to surface waters has been reported. A 1995 study that included early season under-ice water samples that were not available in earlier studies showed that there is, in fact, N leakage to surface waters in some western slope basins. Under-ice nitrate (NO^- ₃) concentrations were as high as 10.5 μeq L^-1 and only decreased to detection limits in September. Landscape type appears to be important in leakage of N to surface waters, which is associated with basins having steep slopes, thin soils, and large amounts of exposed bedrock. NO^- ₃ leakage compounds the existing sensitivity to episodic acidification from low acid neutralizing capacity (ANC), which is less than 40 μeq L^-1 in those basins. [Key words: episodic acidification, nitrogen deposition, nitrate, alpine ecosystems, landscape type, Rocky Mountains.]     

Biomonitoring past salinity changes in an athalassic subarctic lake

A short sediment core was taken from a small saline lake located on an intermontane plateau in the central Yukon Territory, Canada. In July 1990, chemical analyses indicated that, although the lake was shallow (Z_max=1.1 m), it was also chemically stratified, with hyposaline (9.9 to 10.0 g L⁻¹) surface waters and slightly mesosaline (22.0 g L⁻¹) deeper waters. The surface water was dominated by Na⁺ and HCO ₃ ⁻ . To our knowledge, this is the northernmost athalassic saline lake yet recorded. Quantification of algal (diatom, chrysophyte, and pigment) and invertebrate (chironomid, ceratopogonid, andChaoborus) fossils at four stratigraphic levels indicated that the lake sediments preserved numerous biological indicators that could be used to infer recent lake development. Many of the taxa are found in other athalassic salt lakes. The most striking stratigraphic change was a remarkable drop in the species richness of diatoms and invertebrates in the recent sediments, which parallels the elimination of species characteristic of less saline conditions. Halophilous taxa dominate the most recent sediments, indicating the development of more saline conditions. At the same time, a significant shift in chrysophyte cyst composition was observed. Fossil carotenoids and chlorophylls indicated a decrease in total algal abundance in recent sediments, as green and blue-green algae replaced diatoms and chrysophytes. Together, these paleolimnological data suggest a recent shift to drier conditions or increased evaporation in the central Yukon Territory.     

Chemical weathering and CO2 consumption in the Xijiang River basin, South China

Monthly samples of riverine water were collected and analyzed for the concentrations of major ions (Ca²⁺, Mg²⁺, K⁺, Na⁺, HCO₃⁻, SO₄²⁻, Cl⁻, NO₃⁻), dissolved silicon, and total dissolved solids (TDS) at Wuzhou hydrological station located between the middle and lower reaches of the Xijiang River (XJR) from March 2005 to April 2006. More frequent sampling and analysis were carried out during the catastrophic flooding in June 2005. Stoichiometric analysis was applied for tracing sources of major ions and estimating CO₂ consumption from the chemical weathering of rocks. The results demonstrate that the chemical weathering of carbonate and silicate rocks within the drainage basin is the main source of the dissolved chemical substances in the XJR. Some 81.20% of the riverine cations originated from the chemical weathering processes induced by carbonic acid, 11.32% by sulfuric acid, and the other 7.48% from the dissolution of gypsum and precipitates of sea salts within the drainage basin. The CO₂ flux consumed by the rock chemical weathering within the XJR basin is 2.37 × 10¹¹ mol y^− 1, of which 0.64 × 10¹¹ mol y^− 1 results from silicate rock chemical weathering, and 1.73 × 10¹¹ mol y^− 1 results from carbonate rock chemical weathering. The CO₂ consumption comprises 0.38 × 10¹¹ mol during the 9-d catastrophic flooding. The CO₂ consumption from rock chemical weathering in humid subtropical zones regulates atmospheric CO₂ level and constitutes a significant part of the global carbon budget. The carbon sink potential of rock chemical weathering processes in the humid subtropical zones deserves extra attention.     

Water chemistry of some karst environments in Norway

In August 1983, 18 samples were collected in Norwegian karst environments: seepage waters, surface flow upstream sinkholes or caves, allogenic and authigenie karst springs. Hydrochemical data (ion contents and computed variables for CO-CaCO system) are described by means of a factor analysis, the principal components analysis. Four factors, responsible for about 90 % of the total variance, are extracted and interpreted. Five clusters of samples are then identified:

– Authigenic karst waters (seepage and only carbonate aquifer);

– Waters of very short residence time (surface or karst flow);

– CO-rich waters (seepage and possibly organic-rich surface waters), CO2 part is discussed in more detail;

– CO-poor waters (surface waters above tree-line);

– a central group, combining 2 or more of these characters.     

四元体系KCl-K2SO4-KBO2-H2O在298.15 K的Pitzer模型研究

在Pitzer电解质溶液理论的基础上采用两种模型计算了KCl-K₂SO₄-KBO₂-H₂O体系及其子体系的溶解度。模型I假设溶液中只有一种硼物种B(OH)₄^-,模型II假设溶液中有4种硼物种,分别对应于B(OH)₃、B(OH)₄^-、B₃O₃(OH)₄^-和B₄O₅(OH)₄^2-。模型I与模型II的溶解度计算结果接近,且与实验值吻合较好。采用模型II计算了上述体系溶液中的硼物种和OH^-的浓度。各硼物种的浓度主要受溶液中总硼浓度的影响,而很少受KCl和K₂SO₄的影响。计算结果说明在计算偏硼酸钾溶液体系溶解度时,可近似认为溶液中硼物种只有B(OH)_4...     

Geochemistry of waters and brines from the Salinas Grandes basin,Córdoba,Argentina. I. Geomorphology and hydrochemical characteristics

This paper reports on hydrochemical features of diluted waters in the source areas and the brine end-members dominant in the playa of the Salinas Grandes Basin, Córdoba, Argentina. Special emphasis was placed on the study of the relationship between geomorphology and the resulting hydrochemical fractionation. Inflow is from springs and mountain streams which disappear before reaching the saline complex. The playa and intermittent saline lakes are mainly fed by groundwater flow and a few moderately saline and perennial springs. Conversely, ephemeral lakes are fed by atmospheric precipitation and groundwater, whereas small ponds are only fed by atmospheric precipitation. The absence of a clear linkage between geomorphological units and water types was evident in the source areas. Up to four types of water were recognized in a given geomorphological unit. From the sandflat downward towards the playa, the correspondence between geomorphological units and water types was clear, coinciding with a decreased hydrochemical heterogeneity. In this subenvironment, I have recognized two dominant types of water (SO ₄ ^2– –Cl^––HCO ₃ ^– –Na⁺ and Cl^––SO ₄ ^2– –HCO ₃ ^– –Na⁺), which can be considered the original members of the neutral brine in the playa (Cl^––SO ₄ ^2– –Na⁺ where Ca²⁺+Mg²⁺ do not surpass 5 meq per cent), and an intermediate type in the mudflat (Cl^––SO ₄ ^2– –Na⁺ where the contribution of Ca²⁺+Mg²⁺ reaches up to 15 meq per cent). It seems evident that in the zone between the source areas and the sandflat, hydrochemistry is governed by chemical weathering. In stream floodplains and in the distal alluvial plain, close to the saline complex, the increase in water types as well as the increase of HCO ₃ ^– with respect to SO ₄ ^2– , were explained by the mixture of aquifers controlled by the Salinas Grandes-Salinas de Ambargasta fracture. In the saline complex, the more concentrated end-members are the result of evaporation of the two more frequent water-types in the sandflat subenvironment, and salt dissolution of ancient evaporite deposit.     

柴达木盆地北缘冷湖四号构造油田水水化学组成及其分布特征

柴达木盆地北缘冷湖地区赋存大量深部油田水。分析结果显示,冷湖四号构造地区的油田水为CaCl_2型,具有较高Ca含量,一些成分还具有比较明显的区域分异特征。相比柴达木盆地西部,柴北缘油田水的矿化度、K、B、Li等明显偏低。油田水水化学特征系数指示了研究区地层具有良好的封闭性,主要化学组分的富集作用与浓缩作用密切相关。推测碳酸盐、硅酸盐在长期水—岩作用下的溶解对油田水主要化学成分有重要贡献,而区域断裂的发育导致少量样品中的高F含量。     

加拿大海盆的营养盐极大

根据 1 999年和 2 0 0 3年中国北极科学考察航次 ,从Canada海盆收集温、盐、深和营养盐浓度数据 ,用文献报道的低浓度1 2 9I和高浓度金属钡 (Ba)来指示太平洋源水、用相应的高浓度1 2 9I和低浓度Ba来指示大西洋源水 ,划分了该海盆物理化学特征的 4个水团。表层水 ( <40m)的盐度从 2 5至 31 .6;硝酸盐处于耗尽水平 ,而磷酸盐和硅酸盐处于最低水平。营养盐再生水大致位于 40- 2 0 0m ;盐度特征为 31 .6- 33.1 ;营养盐浓度一致增至最高 ;极大峰的盐度在 33.1附近 ,其位温则处于最低水平 (约 - 1 .5°C)。混合水 (深约 2 0 0- 385m)盐度从 33.1至 34.8;位温从局域最低升至整个水柱最高的 0 .5 0- 0 .65 7°C ;营养盐则逐渐降低。深层水深度变化较大 ( 385m至 1 90 0m以下海底 ) ;但其盐度变化较小 ( 34.8- 34.9) ;位温则从最高降低到 - 0 .4至 - 0 5 4°C ;营养盐均轻微增加。结合文献中对于营养盐极大的年际观测 ,1 2 9I、Ba与氯氟烃CFC 1 1的浓度及3H 3He示踪年龄的结果分析表明 ,营养盐再生水是无季节性变化的、高年龄 (约 8- 1 5年 )的太平洋源水 ;深层为大西洋源水 ;而混合水团即为上述 2大源水的混合层。硅酸盐和磷酸盐的强极大指示优势种硅藻及其再生主导太平洋源水。     

The role of biogeochemical cycling for the formation and preservation of varved sediments in Soppensee (Switzerland)

We analyzed seasonally aggregated observations of temperature, conductivity, dissolved oxygen and dissolved inorganic carbon from Soppensee (District of Lucerne, Switzerland) for the yrs 1980 to 1993. Holomictic Soppensee is characterized by a strong summer stratification with a thin epilimnion separated from an anoxic hypolimnion by a strong pycnocline formed by thermal and chemical gradients. A vertical one-dimensional model was developed to simulate the observed seasonal cycles of carbon and oxygen. The processes of net community production, mineralization of organic matter, precipitation and dissolution of calcite, gas exchange, in- and outflow, sedimentation and vertical eddy diffusion are included. According to the model, the annual net community production is estimated to about 110 g C m^-2 yr^-1 and the annual net primary production to about 330 to 440 g C m^-2 yr^-1, which is a typical value for eutrophic lakes. A mass balance of the carbon cycle indicates that most of the inflow comes from groundwater which is super-saturated with respect to atmospheric CO₂. Therefore the surface waters exhibit a large capacity for calcite precipitation. The results of the model are used to constrain the conditions that favor the formation of varved sediments in Soppensee during thousands of yrs. Model calculations show that the deep waters would still turn anoxic even if the sedimentation rate of organic matter were decreased to 25%. Several physical factors such as biogenic stabilization of the deep waters due to calcite dissolution and low input of wind energy are responsible for the long term anoxia in Soppensee.