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1.
Five soil samples collected from shooting ranges in 1998 were stored under a closed condition for 5 years. In addition to SEM and XRD investigations, the total organic carbon content (TOC), inorganic carbon content (TIC), δ13C and δ18O of carbonates and δ13C of plant remains were analyzed. The concentrations of total carbon contents, the sum of TOC and TIC, remained the same within the 5 years storage, whereas the TOC and TIC contents decreased and increased, respectively. The TIC increase is associated with a decreased TOC, suggesting a conversion of organic carbon into inorganic carbon. Such a conversion is evidenced by the presence of primary lead carbonates and carbon isotopic composition of lead carbonates. It can be concluded that soil organic matters play an important role in the process of bullets weathering and controls migration of the elevated lead in the soil.  相似文献   

2.
碳酸盐岩有机质丰度测试新方法   总被引：2，自引：0，他引：2  
常规有机碳测试中仅对残余固相进行测试而忽略了酸解液,而前人研究证实酸解液中含有一定量的有机质。为了准确定量碳酸盐岩样品的总有机碳(TOC),提出蒙脱石增稠元素分析的新方法。本次研究以配比标样(CaCO3+SiO2+有机质标样)作为研究对象,对配比标样进行传统有机碳测试以及酸解后利用蒙脱石增稠进行元素分析的新方法测试。结果显示加入有机质标样为小分子有机酸(盐)的配比标样的传统有机碳测试的相对误差为98.5%~99.6%,加入大分子有机质的配比标样传统有机碳测试的相对误差较小,为11.9%~48.1%。而酸解后蒙脱石增稠进行元素分析测试的方法中,总有机碳(TOC)的相对误差为0.76%~19.46%。不同有机碳浓度的配比标样的元素分析法测试结果的相对误差随着有机碳浓度的增大而减小。新有机碳测试方法中,由于除去无机碳后将残渣与酸解液混合均匀并增稠,避免了有机碳的流失,更能客观反映样品总有机碳(TOC)。  相似文献   

3.
湖泊沉积物中的总有机碳含量(TOC)、总有机氮含量(TN)和碳氮比值(C/N)已被广泛应用于第四纪湖泊古环境研究中。对湖泊沉积物样品进行TOC和TN测定前, 首先要有效去除沉积物中的无机碳酸盐, 同时较好地保留有机质组分, 才能使实验结果较准确地反映古气候环境的变化。选取鹤庆钻孔不同深度的不同岩性样品, 分别进行粒度、盐酸浓度、洗除残留酸方法等对去除碳酸盐和总有机碳测定结果影响的前处理条件实验, 根据测得的TOC、TN和C/N, 结合总无机碳酸盐含量(TIC), 确定了鹤庆钻孔沉积物有机碳含量测定的前处理方法:室温条件下, 将磨得足够细(无需过筛处理)的样品与足量浓度为2mol/L盐酸充分反应24小时, 期间超声震荡3次, 采用离心加速沉淀的方法清洗酸处理样品至中性, 烘干, 研磨均匀上机测定。结果显示, 该流程可有效去除沉积物中的无机碳酸盐, 测得的TOC、TN数值具有很好的稳定性和可重复性。在此基础上测定了鹤庆钻孔沉积物样品的TOC、C/N和TIC, 它们间存在很好的正相关关系, 指示了西南季风强度的变化。   相似文献   

4.
中世纪暖期前后我国雷洲半岛地区的古气候变化   总被引：1，自引：0，他引：1  
本文对位于雷洲半岛湖光岩玛珥湖湖沉积物进行了年代学(137Cs、AMS 14C)及总碳(TC)、氮(TN)、无机碳(IC)的分析。对于湖光岩玛珥湖这一热带地区封闭湖泊而言,无机碳含量的变化可能受降水量-蒸发量控制。有机碳、氮的变化可能反映了湖泊生产率及营养状况的变化。在热带地区,湖水温度变化不大,温度可能不是藻类生长的主要控制因素,降水量的增加及湖泊营养物质的变化可能是有机碳、氮含量增加的主要原因。碳酸盐含量的高值期对应于有机碳、氮的低值阶段。1400a来碳酸盐含量有两个高值阶段,分别为AD 880~1260和AD 670~760.这两个高值阶段可能也是干旱期。湖光岩玛珥湖地球化学指标所揭示的干旱期与安徽龙感湖硅藻和孢粉的研究结果有较好的对应性,可能表明我国南部地区中世纪暖期可能存在一个干旱期。   相似文献   

5.
In a comprehensive study, we compared depositional conditions, organic matter (OM) composition, and organic carbon turnover in sediments from two different depositional systems along the Chilean continental margin: at ∼23° S off Antofagasta and at ∼36° S off Concepción. Both sites lie within the Chilean coastal upwelling system and have an extended oxygen minimum zone in the water column. However, the northern site (23° S) borders the Atacama Desert, while the southern site (36° S) has a humid hinterland. Eight surface sediment cores (up to 30 cm long) from water depths of 126-1350 m were investigated for excess 210Pb (210Pbxs) activity, total organic and total inorganic carbon concentrations (TOC and TIC, respectively), C/N-ratios, organic carbon isotopic compositions (δ13C), chlorin concentrations, Chlorin Indices (CI), and sulfate reduction rates (SRR). Sediment accumulation rates obtained from 210Pb-analysis were similar in both regions (0.04-0.15 cm yr−1 at 23° S, 0.10-0.19 cm yr−1 at 36° S), although total 210Pbxs fluxes indicated that the vertical particle flux was higher at 36° S than at 23° S. We propose that sediment focusing in isolated deposition centers led to high sediment accumulation rates at 23° S. Furthermore, there were no indications for sediment mixing at 23° S, while bioturbation was intense at 36° S. δ13C-values (−24.5‰ to −20.1‰ vs. VPDB) and C/N-ratios (molar, 8.6-12.8) were characteristic of a predominantly marine origin of the sedimentary OM in both investigated areas. The extent of OM alteration in the water column was partly reflected in the surface sediments as chlorin concentrations decreased and C/N-ratios and CI increased with increasing water depth of the sampling site. SRR were lower at 23° S (areal SRR 0.12-0.60 mmol m−2 d−1) than at 36° S (areal SRR 0.82-1.18 mmol m−2 d−1), which was partly due to the greater water depth of most of the sediments investigated in the northern region and consistent with a lower quality of the sedimentary OM at 23° S. Reaction rate constants for TOC degradation that were obtained from measured SRR (kSRR; 0.0004-0.0022 yr−1) showed a good correspondence to kTOC that were derived from the depth profiles of TOC (0.0003-0.0014 yr−1). Both, kSRR and kTOC, reflect differences in OM composition. At 36° S they were related to the degradation state of bulk OM (represented by C/N-ratios), whereas near 23° S they were related to the freshness of a small fraction of labile OM (represented by CI). Our study shows that although rates of organic carbon accumulation were similar in both investigated sites, the extent and kinetics of organic carbon degradation were closely linked to differing depositional conditions.  相似文献   

6.
This study reports the first ethanol and acetaldehyde measurements in sediment porewaters collected at multiple freshwater locations. Ethanol concentrations ranged from 11 to 2535 nM and acetaldehyde concentrations ranged from 6 to 320 nM. A significant positive correlation (p < 0.001) was observed between ethanol concentrations and the percent organic carbon content of sediments (TOC). Porewater depth profiles at two sites within the same lake indicated potential diffusion of ethanol into sediments from the overlying water at a lower TOC site and upwards diffusion from sediment into the water column at a higher TOC site. Diffusion of water column ethanol into sediments was observed at individual sites from October to January, whereas the opposite was true from June to August indicating the seasonal variability of ethanol flux from sediments. Changes in ethanol concentrations during a long-term sediment incubation experiment showed an inverse relation with acetaldehyde concentrations. The lack of a quantitative conversion was likely due to other sources and sinks that control their abundance. Our study provided new information on the biogeochemistry of ethanol in freshwater sediments and shed light on the potential role of ethanol in the global carbon cycle.  相似文献   

7.
结合骆驼山煤矿不同含水层水文地质条件,通过检测分析各含水层水中天然有机质三维荧光光谱、总有机碳TOC和无机阴离子,研究了荧光性溶解有机物(Dissolved Organic Matter,DOM)的分布特征,结果表明:TOC和有机物在254 mm波长紫外光下的吸光度UV254整体上随着含水层层位加深而减少,奥灰水中TOC和UV254比其他水体分别低2~3.3倍和2.4~4.7倍;有机物芳香度也逐渐降低,紫外吸光度SUVA值在地表水、第四系水、砂岩水和奥灰水中分别为3.28、2.27、2.24和1.96。地表水和第四系水的三维荧光光谱(3DEEM)图存在5个指纹区域,随着地层层位的加深,水中有机物总体上呈递减趋势,最深层的奥灰水中没有酪氨酸、疏水性有机酸和海洋性腐植酸,而色氨酸的荧光强度比其他水体都高,表明地下水中有机物会反应生成色氨酸类有机物。奥灰水中TOC随着地下水流向逐渐减少(从0.27 mg/L减少至0.22 mg/L);有机物反应生成色氨酸,导致色氨酸FI随着水流而逐渐增加;根据3DEEM光谱图,骆驼山煤矿区奥灰水中有机物比较稳定,能够明显区分出其作为突水水源的特征离子。   相似文献   

8.
《Applied Geochemistry》1993,8(5):483-493
Information regarding the origin, composition and transport of natural dissolved organic carbon (DOC) in groundwater is necessary to understand the transport of metals and organic pollutants, as well as for the use of14C in DOC as an isotopic groundwater dating method. Previous research in several groundwater systems has suggested soil organic C is the predominant source of high molecular weight DOC to the subsurface. Through the use of stable isotopes,14C and geochemical analyses, this study shows that significant concentrations of DOC and CH4 in a regional confined aquifer can be generated in situ from subsurface sedimentary organic sources. The DOC and CH4 produced is a combined result of degradation of buried peats and bacterial action, resulting in high DOC concentrations and strongly methanogenic conditions in the aquifer. The DOC and CH4 comprise, on average, nearly 50% of the total dissolved C pool in the central part of the aquifer. Methanogenic conditions complicate isotopic groundwater dating by the conventional dissolved inorganic carbon (DIC) method. Estimates of isotopic groundwater residence time using DOC14C data are proposed by the application of14C isotope and mass balance corrections.  相似文献   

9.
The aim of this study was to investigate the water and sediment quality in the mid-Black Sea coast of Turkey. The samples were collected from six stations during 2007. Investigated parameters were total carbon (TC), total inorganic carbon (TIC), total organic carbon (TOC), ammonium-nitrogen (NH4-N), nitrate-nitrogen (NO3-N), nitrite-nitrogen (NO2-N), total phosphorus (TP), sulphate, total hardness, methylene blue active substances (MBAS), phenol, adsorbable organic halogens (AOX), dissolved oxygen (DO), pH and electrical conductivity (EC) in water samples and TC, TIC, TOC, TP, pH, electrical conductivity (EC), redox potential (Eh) and water content (WC) in sediment samples. Different multivariate statistical techniques were used to evaluate variations in surface water and sediment quality. Principal component analysis helped in identifying the factors or sources responsible for water and sediment quality variations. Five factors were found responsible for 87.63% of the total variance in the surface waters. In sediments, three factors explained 84.73% of the observed total variance. Cluster analysis classified the monitoring sites into two groups based on similarities of water and sediment quality characteristics.  相似文献   

10.
A water-chemistry evaluation was made of the available springs and wells in Amman and vicinity. Trihalomethanes (THM) were found in all analysed samples with concentrations ranging from 0.2–31.88 μg/L. The probable sources of trihalomethanes in the aquifers originate from three sources: (1) chlorinated Deir Alla surface water, (2) reaction of excess chlorine in the leaky, corroded water-distribution network with organic matter in the vadose zone, and (3) sewage seepage from cesspools in the area. Total organic carbon (TOC) ranged from 0.2–1.4 mg/L. Its probable source is either from the vadose zone or the treated surface water at Deir Alla. It was found that TOC was of vital importance in the formation of THM in the presence of chlorine from the water-distribution system. Major ionic composition of the analysed samples reflected the limestone lithology of the aquifer in the investigated area. Heavy-metal content was relatively low due to the high pH of the groundwater samples. Electronic Publication  相似文献   

11.
High iron concentrations create water quality problems for municipal use in glacial drift aquifer units. The chemical evolution of oxic groundwater in shallow aquifer units to anoxic groundwater in deeper aquifer units, in which soluble Fe(II) is stable, is attributed to coupled reduction of Fe(III) on aquifer solids with oxidation of organic carbon. The objective of this study was to characterize the distribution of organic carbon in aquifer and aquitard sediments to determine the availability of potential electron donors to drive these reactions. To do this, four complete rotasonic cores in a glacial aquifer/aquitard system were sampled at close intervals for analyses of grain-size distribution and organic carbon content. The results indicate significantly higher organic carbon concentrations in diamicton (till) units that function as aquitards, relative to coarse-grained aquifer units. In addition, readily reducible iron content in the diamicton units and lower aquifer unit materials is sufficient to produce far more dissolved iron than is present in the aquifer. Groundwater evolves to the level of iron reduction as a terminal electron-accepting process as it moves downward through aquitard units along flow paths from upland recharge areas to downgradient discharge areas. Deeper aquifer units are therefore unlikely to contain groundwater with low iron concentration.  相似文献   

12.
王尧  田衎  封跃鹏  王伟 《岩矿测试》2021,(4):593-602
土壤环境标准样品是土壤生态环境监测质量控制的重要技术工具。目前,土壤中总有机碳环境标准样品仍为中国环境标准样品体系的空缺,特别是配套燃烧氧化-非分散红外法的土壤标准样品一直未曾问世。本文以有机碳含量较高的农用地土壤为原材料,经干燥、研磨、混匀、装瓶、灭菌等加工步骤,制备获得土壤中总有机碳环境标准样品。分层随机抽取10瓶样品进行均匀性检验,经评价统计量F小于临界值F_(0.05)(9,10),瓶间均匀性相对不确定度(u_(bb))为1.5%,样品均匀性良好。在室温避光保存条件下,对样品进行了18个月的稳定性检验,稳定性相对不确定度(u_(lts))为1.2%,样品具有良好稳定性。由中国11家实验室采用燃烧氧化-非分散红外法和重铬酸钾容量法进行协作定值,通过对检测结果的数理统计分析,样品量值评定结果为(25.2±1.4)mg/g。该标准样品为采用燃烧氧化-非分散红外法参与定值的土壤中总有机碳环境标准样品,可作为土壤中总有机碳测定标准方法配套的实物标准,满足土壤生态环境监测及相关研究需求,且与国外同类样品具有可比性。  相似文献   

13.
Bacterial abundance and production, numbers, sizes and concentrations of transparent exopolymer particles (TEP) and total organic carbon (TOC) were measured during the 1996 summer monsoon to understand the relationship between TEP, the most labile particulate organic carbon, and bacteria. While high regional variability in the vertical distribution of TOC was discernible, TEP concentrations were high in surface waters at 18–20°N along 64°E with concentrations well over 25 mg alginic acid equivalents I−1 due to upwelling induced productivity. Their concentrations decreased with depth and were lower between 200 and 500 m. Bacterial concentrations were up to 1.99 × 108 I–1 in the surface waters and decreased by an order of magnitude or more at depths below 500 m. A better relationship has been found between bacterial abundance and concentrations of TEP than between bacteria and TOC, indicating that bacterial metabolism is fueled by availability of TEP in the Arabian Sea. Assuming a carbon assimilation of 33%, bacterial carbon demand (BCD) is estimated to be 1.017 to 4.035 g C m–2 d–1 in the surface waters. The observed TEP concentrations appear to be sufficient in meeting the surface and subsurface BCD in the northern Arabian Sea.  相似文献   

14.
In this study, attenuated total reflectance (ATR) Fourier transform infrared spectroscopy (FTIR) was coupled with partial least squares regression (PLSR) analysis to relate spectral data to parameters from total organic carbon (TOC) analysis and programmed pyrolysis to assess the feasibility of developing predictive models to estimate important organic geochemical parameters. The advantage of ATR-FTIR over traditional analytical methods is that source rocks can be analyzed in the laboratory or field in seconds, facilitating more rapid and thorough screening than would be possible using other tools. ATR-FTIR spectra, TOC concentrations and Rock–Eval parameters were measured for a set of oil shales from deposits around the world and several pyrolyzed oil shale samples. PLSR models were developed to predict the measured geochemical parameters from infrared spectra. Application of the resulting models to a set of test spectra excluded from the training set generated accurate predictions of TOC and most Rock–Eval parameters. The critical region of the infrared spectrum for assessing S1, S2, Hydrogen Index and TOC consisted of aliphatic organic moieties (2800–3000 cm−1) and the models generated a better correlation with measured values of TOC and S2 than did integrated aliphatic peak areas. The results suggest that combining ATR-FTIR with PLSR is a reliable approach for estimating useful geochemical parameters of oil shales that is faster and requires less sample preparation than current screening methods.  相似文献   

15.
Impacts of subsurface heat storage on aquifer hydrogeochemistry   总被引：3，自引：3，他引：0  
The use of shallow aquifers for subsurface heat storage in terms of energy management and building climatisation can lead to a temperature rise in the aquifer to 70 °C and above. The influence of temperature changes on individual mineral and sorption equilibria, reaction kinetics and microbial activity is largely known. However, the impact of heating to temperatures as high as 70 °C on the aquifer overall system has not been quantified yet. Temperature-related changes in sediment ion exchange behaviour, dimension and rates of mineral dissolution and precipitation as well as microbially enhanced redox processes were studied in column experiments using aquifer sediment and tap water at 10, 25, 40, and 70 °C. At 70 °C, a change in sediment sorption behaviour for cations and organic acids was postulated based on temporal changes in pH, magnesium, and potassium concentration in the experimental solution. No clear changes of pH, TIC and major cations were found at 10–40 °C. Redox zoning shifted from oxic conditions towards nitrate and iron(III) reducing conditions at 25 and 40 °C and sulphate reducing conditions at 70 °C. This was attributed to (a) a temperature-related increase in microbial reduction activity, and (b) three times higher release of organic carbon from the sediment at 70 °C compared to the lower temperatures. The findings of this study predict that a temperature increase in the subsurface up to 25 °C and above can impair the usability of ground water as drinking and process water, by reducing metal oxides and thus possibly releasing heavy metals from the sediment. Generally, at 70 °C, where clear cation and organic carbon desorption processes were observed and sulphate reducing conditions could be achieved, a site-specific assessment of temperature effects is required, especially for long-term operations of subsurface heat storage facilities.  相似文献   

16.
Total Hg concentrations have been measured for five box-core sediments collected seawards of the Augusta industrial area (SE Sicily). In more coastal sediments, upcore increasing Hg concentrations, exceeding the Hg background concentration estimated for the Strait of Sicily, indicate Hg contamination over time due to the industrial area development. Strong correlation between total organic C (TOC) and Hg concentrations was found only for core BX2, that displays organic C to total N (C/N) ratios indicative of autochthonous organic matter. For other sediments, high Hg enrichment factors with respect to TOC indicate, in addition to Hg trapping by TOC, other factors as responsible for Hg accumulation. In the presence of some contribution of detrital organic matter, Hg is mainly adsorbed onto the mineral component of the bottom sediments probably because TOC is saturated by Hg excess. Contaminant impact affected also the open sea environment. Main drivers of Hg flux towards the offshore were dredged materials, which repeatedly discharged sediment, resulting in substantial increases in TOC contents and high C/N ratios. Consistent with the geochemistry of recent turbidites, these anomalous sedimentary inputs induced sediment redox environment modifications, constrained by Mn peaks, which affected Hg distribution.  相似文献   

17.
海相高演化烃源岩总有机碳恢复系数研究   总被引：12，自引：0，他引：12  
在5000余块海相烃源岩样品筛选结果的基础上, 根据90余块不同类型未成熟-成熟烃源岩的加水热压模拟实验结果, 并与自然演化剖面相结合, 对烃源岩有机质的变化规律及其恢复系数进行研究.海相优质烃源岩在未成熟-低成熟阶段(Ro < 0.8%) TOC (totalorganiccarbon) 变化不明显, 在成熟阶段中晚期TOC残余随成熟度增加逐渐降低, 到高成熟-过成熟阶段变化又不明显.高成熟-过成熟优质烃源岩TOC原始一般Ⅰ型最高降低40%, 恢复系数1.68;Ⅱ1型最高降低32%, 恢复系数1.48;Ⅱ2型最高降低24%, 恢复系数1.32.低有机质烃源岩(一般指0.3% < TOC < 1%) 随TOC变低, 降低幅度和恢复系数均逐渐变小, 当0.3% < TOC < 0.5%时, TOC原始恢复系数约1.2, 当TOC < 0.3%时, TOC原始恢复系数接近1, 可以不进行恢复.固体沥青和高有机质页岩(TOC > 30%) TOC原始高成熟-过成熟阶段也不需要进行恢复.海相烃源岩(0.3% < TOC < 30%) 自然剖面生烃潜量的减少和模拟生排烃量的增加与TOC残余的减少相吻合.   相似文献   

18.
探讨了河西走廊石羊河终端湖泊--猪野泽晚冰期以来沉积物总有机碳(TOC)、碳氮比(C/N)、有机碳同位素(δ13C)三种有机地球化学指标之间的关系及古环境意义.结果表明:猪野泽QTH01剖面沉积物TOC指标主要代表湖泊及流域的植被初级生产力;C/N值受到周围区域表土C/N值和沉积物成岩过程的双重影响,总体较低,并不能直...  相似文献   

19.
Detailed chemostratigraphy across the Cenomanian-Turonian boundary in northern Tunisia points to several prevailing paleoceanographic conditions during the deposition of organic-rich beds of Bahloul Formation. The sedimentological study shows that there is no correlation between color and CaCO3 content because both dark and light-colored intervals of Bahloul Formation are carbonate-rich. Stable isotope analysis displays a positive carbon isotope excursion characterized by four significant peaks (I to IV) which are ranging from 3.2 to 3.5‰. These peaks represent episodes of elevated rates of organic carbon burial during the C/T oceanic anoxic event (C/T boundary OAE2). The Cenomanian-Turonian boundary could be situated between the third isotopic peak and the filament event. The total organic carbon (TOC) measurements show values ranging from 0.28 to 6.19% with average value of 3.5%. This indicates that the Bahloul Formation shale is a very good oil source rock. The Hydrogen Index (HI) values range from 359 to 698 mg HC/g TOC. The T max values range from 390 to 438 °C. Binary diagrams HI vs. T max indicate a type II with values falling within the immature organic-matter range. The concentrations major elements reveal low values of Ti and K. The correlation between Al and Ti and K shows a significant correlation pointing to homogeneous provenance. Primary productivity indicators (Cu, Ba, and Ni) record its association with organic matter. Redox-sensitive elements such as U, V, and Mo and the high values of V/(V + Ni) ratio indicate a strongly reducing environment which led to the better preservation of the organic matter.  相似文献   

20.
The 25th cruise of R/FAkademik Knipovitch conducted in January–April of 1990 comprised investigations of total organic carbon (TOC) at the following sections: through the Polar Frontal Zone (PFZ) along 40° W, made in January and April; from the PFZ to the South Orkney Islands, and on the South Georgia shelf. The measurements made comprised TOC, organic nitrogen, nitrate, nitrite, ammonium nitrogen, phosphate and silicate.The surface waters of the region were characterized by high heat content, which influenced the Antarctic phytosynosis function. The data obtained showed low content of organic matter (OM); high content of TOC, rising up to 3,5 mg m–3, was recorded at the photic layer and in the layer of OM accumulation, at the upper boundary of the Antarctic Deep Waters and the vertical boundaries of the Antarctic Intermediate Waters. The South Georgia shelf waters showed even distribution of TOC, about 0,2 mg m–3, being under the influence of the south periphery of the ACC waters.  相似文献   

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