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1.
S. L. Wang C. Y. Lin X. Z. Cao X. Zhong 《International Journal of Environmental Science and Technology》2012,9(1):31-40
The Nansi Lake has been seriously affected by long-term intensive industrial and urban activities. The objectives of this study were to determine the content, distribution, and ecological risk of arsenic and investigate the geochemical relationships between arsenic forms and sediment mineral phases of the Nansi Lake. Twenty samples of surface sediments were collected and analyzed for arsenic contents and chemical forms. Results indicated that total content of arsenic in the sediment samples averaged 13.45?mg/kg and ranged from 8.27 to 21.75?mg/kg. The arsenic was mostly associated with iron oxides (67.3%), followed by the association with the residual fraction (19.2%). In addition, total content of arsenic was positively correlated with the organic matter and iron contents in the sediment. The molar ratios of iron oxide bound arsenic content to iron content are lower than the maximal molar ratios of arsenic to iron for natural hematite, magnetite, and goethite. The total content of arsenic in the sediment samples was usually higher than threshold effect concentration of 9.79?mg/kg, but lower than probable effect concentration of 33.0?mg/kg for arsenic in freshwater sediments. Adverse effects or toxicity to the aquatic organisms, caused by arsenic in the sediments of the Nansi Lake, will likely occur at these levels of arsenic contamination. 相似文献
2.
The adsorption of phosphorus on natural diagenetic iron (Feox) and manganese (Mnox) oxyhydroxides was studied in deep and littoral zone sediments of mesotrophic Lac Saint-Charles (46°56 N, 71°23 W), using a Teflon sheet technique for collecting diagenetically produced metal oxyhydroxides. Collected metal oxide amounts were greater at the deep-water station, relative to littoral zone stations reflecting sediment and local diagenetic differences. Two-layer surface complexation modeling on iron oxyhydroxide was consistent with the measured total P/Fe molar ratios except for the upper mixed Mn–Fe oxide layer from the littoral stations, where measured phosphorus exceeded the modeled phosphorus by more than fivefold. Soluble reactive phosphorus (SRP) exchange between oxyhydroxide samples and natural lake water in the laboratory revealed a labile phosphorus pool. Phosphorus determined on the Teflon sheets from the littoral zone stations appears to be related to a distinct non-humic organic carbon pool that readily exchanges SRP, while little exchange was observed from material collected from the deep-water station. We suggest that the enhanced SRP release from littoral zone sediments is due to an organic carbon and/or metal oxide-impoverished sediment matrix, limiting microbial oxide reduction and allowing phosphorus to be rapidly recycled at the sediment–water interface, instead of being slowly incorporated into humic material. The SRP fluxes revealed in our study, which originate from the solid phase at the sediment–water interface, would be difficult to resolve using interstitial pore-water samplers and might be a quantitatively important source of inorganic phosphorus in Shield lakes. 相似文献
3.
Françoise Andrieux-Loyer Afi Azandegbé Florian Caradec Xavier Philippon Roger Kérouel Agnès Youenou Jean-Louis Nicolas 《Aquatic Geochemistry》2014,20(6):573-611
This study aims to compare the impact of oyster cultures on diagenetic processes and the phosphorus cycle in the sediments of the Aber Benoît and the Rivière d’Auray, estuary of Brittany, France. Our results showed clear evidence of the seasonal impact of oyster cultures on sediment characteristics (grain size and organic matter parameters) and the phosphorus cycle, especially in the Aber Benoît. At this site, seasonal variations in sulfide and Fe concentrations in pore waters, as well as Fe–P concentrations in the solid phase, highlighted a shift from a system governed by iron reduction (Reference) to a system governed by sulfate reduction (beneath oyster). This could be partly explained by the increase in labile organic matter (i.e., biodeposits) beneath oysters, whose mineralization by sulfate led to high sulfide concentrations in pore waters (up to 4,475 µmol l?1). In turn, sulfide caused an enhanced release of phosphate in the summer, as adsorption sites for phosphate decreased through the formation of iron–sulfide compounds (FeS and FeS2). In the Aber Benoît, dissolved Fe/PO4 ratios could be used as an indicator of phosphate release into oxic water. Low Fe/PO4 ratios in the summer indicated higher effluxes of phosphate toward the water column (up to 47 µmol m?2 h?1). At other periods, Fe/PO4 ratios higher than 2 mol/mol indicated very low phosphate fluxes. In contrast, in the Rivière d’Auray, the occurrence of macroalgae, stranding regularly all over the site, clearly masked the impact of oyster cultures on sediment properties and the phosphorus cycle and made the use of Fe/PO4 ratios more difficult in terms of indicators of phosphate release. 相似文献
4.
《Applied Geochemistry》1998,13(4):451-462
Water, suspended matter, and sediment samples were taken from 8 locations along the Yangtze River in 1992. The concentration and speciation (exchangeable, bound to carbonates, bound to Fe–Mn oxides, bound to organic matter, and residual forms) of rare earth elements (La, Ce, Nd, Sm, Eu, Tb, Yb, and Lu) were determined by instrumental neutron activation analysis (INAA).The contents of the soluble fraction of REEs in the river are low, and REEs mainly reside in particulate form. In the particles, the chondrite-normalized distribution patterns show significant LREE enrichment and Eu-depletion. While normalized to shales, both sediments and suspended matter samples show relative LREE enrichment and HREE depletion. REEs are relatively enriched in fine-grained fractions of the sediments.The speciation characteristics of REEs in the sediments and suspended matter are very similar. The amount of the five forms follows the order: residual>>bound to organic matter∼bound to Fe–Mn oxides>bound to carbonates>>exchangeable. About 65 to 85% of REEs in the particles exist in the residual form, and the exchangeable form is very low. High proportions of residual REEs reveal that REEs in sediments and suspended matter are controlled by their abundances in the earth's crust. Carbonate, Fe–Mn oxide and organic fractions of REEs in sediments account for 2.4–6.9%, 5.2–11.1%, and 7.3–14.0% of the total contents respectively. They are similar to those in the suspended matter. This shows that carbonates, Fe–Mn oxides and organic matter play important roles during the particle-water interaction processes. By normalization to shales, the 3 forms of REEs follow convex shapes according to atomic number with middle REE (Sm, Eu, and Tb) enrichment, while light REE and heavy REE are depleted. 相似文献
5.
LIU Chunlian Wolfgang OSCHMANN BAI Yan DONG Yixin XIE Yecai Department of Earth Sciences Sun Yat-Sen 《《地质学报》英文版》2004,78(3):768-774
Analyses of organic carbon, nitrogen, sulfur and iron have been performed in order to understand sources and preservation of organic matter in black shale of the Buxin Formation (Early Paleogene) from the Sanshui Basin. The C/N ratios show that the organic matter is characterized by a mixture of terrestrial and phytoplanktonic contributions. The relative importance of different sources depend on climate conditions and most of organic matter is of terrestrial origin. The relationships between C, S and Fe indicate that the brackish environment with alternation of anoxia and low-O2 developed in the bottom waters during the deposition of these organic-rich sediments as a result of a mixed setting of thermal stratification and salinity stratification, the latter being the consequence of intermittent sea water incursion. Bacterial sulfate reduction is the most effective early diagenesis affecting the preservation of organic matter. The intensity of sulfate reduction is related to the relative proportion of met 相似文献
6.
Incubation experiments were adopted to characterize the rates and pathways of iron reduction and the contributions to anaerobic organic matter mineralization in the upper 0–5 cm of sediments along a landscape-scale inundation gradient in tidal marsh sediments in the Min River Estuary, Southeast China. Similar sediment characteristics, single-species vegetation, varied biomass and bioturbation, distinct porewater pH, redox potential, and electrical conductivity values have resulted in a unique ecogeochemical zonation along the inundation gradient. Decreases in solid-phase Fe(III) and increases in nonsulfidic Fe(II) and iron sulfide were observed in a seaward direction. Porewater Fe2+ was only detected in the upland area. High rates of iron reduction were observed in incubation jars, with significant accumulations of nonsulfidic Fe(II), moderate accumulations of iron sulfides, and negligible accumulations of porewater Fe2+. Most of the iron reduction was microbially mediated rather than coupled to reduced sulfides. Microbial iron reduction accounted for 20–89 % of the anaerobic organic matter mineralization along the inundation gradient. The rate and dominance of microbial iron reduction generally decreased in a seaward direction. The contributions of microbial iron reduction to anaerobic organic matter mineralization depended on the concentrations of bioavailable Fe(III), the spatial distribution of which was significantly related to tidal inundation. Our results clearly showed that microbial iron reduction in the upper sediments along the gradient is highly dependent on spatial scales controlled primarily by tidal inundation. 相似文献
7.
Arie Nissenbaum 《Geochimica et cosmochimica acta》1979,43(12):1973-1978
The phosphorus content of marine humic acids (HA) is in the range of 0.1–0.2%. The C/P ratios of the HA are 300 to 400. Marine fulvic acids (FA) contain 0.4–0.8% P and have C/P ratios of 80 to 100. High molecular weight organic matter dissolved in pore waters (DOM) contains 0.5% P and has C/P of 90. The data suggest that during the formation sequence: Plankton → DOM → FA → HA → Kerogen, phosphorus is lost, mainly in the FA → HA (and possibly also in the HA → Kerogen) step. Diagenesis of sedimentary humic acids is accompanied by loss of phosphorus (as well as of nitrogen) to form HA with C/P ratios of 1000.Soil humic substances resemble marine humates in P content (0.3%) and soil FA's are about three to fivefold enriched in P relative to HA. C/P ratios are lower in soil HA (ca. 200) as compared with marine HA. Humic acids from diagenetic products such as peat and lignite are highly depleted in P. Rough calculations indicate that humate bound P may account for 20–50% of the organic phosphorus reservoir in sediments. The chemical speciation of this P is unknown, but lack of correlation with ash, Fe, Ca or Al content (in marine humates, at least) indicates that it is organically bound. 相似文献
8.
热液活动对东二沟剖面玉尔吐斯组烃源岩形成的影响 总被引：1，自引：0，他引：1
研究热液活动是否会破坏烃源岩的形成。对塔里木盆地东二沟剖面玉尔吐斯组进行地球化学分析,利用δEu、Fe/Ti和（Fe+Mn）/Ti比值研究热液活动,Al/Ti比值替代古生产力,V/Cr、V/（V+Ni）和Ni/Co比值代表氧化还原环境,进而探讨热液活动与古生产力、氧化还原条件以及有机质含量之间的关系。玉尔吐斯组沉积时古生产力水平较低,为贫氧-厌氧环境,下部具有较强的热液活动,中上部热液活动较弱。下部的热液活动虽然促进了古生产力的提高,但TOC含量整体较低,为0.01%～3.58%,平均值为0.64%;中上部热液活动较弱,古生产力水平较低,TOC含量却较高,为0.06%～12.19%,平均值为8.95%,是较好的烃源岩层。岩石薄片显示,与热液活动相关的硅质岩中含有大量的藻类。研究结果表明,较强的热液活动会带来大量的富硅流体,稀释沉积物中的有机质,对烃源岩的形成起破坏作用。 相似文献
9.
长江口及其邻近海域孔隙水地球化学特征 总被引：1，自引：0，他引：1
对长江口沉积物有机碳、总氮、总磷、Fe、Mn、AI及孔隙水和上覆水体中营养盐、Fe、Mn的含量进行了测试,结合早期成岩模型及地球化学热力学分析,探讨了在河口环境中影响孔隙水营养盐和Fe、Mn分布的主要因素,并对沉积物-水界面营养盐扩散通量进行了估算。结果表明,孔隙水中NH4^＋、NO3^-、PO3^4、H4SiO4和Fe、Mn的含量显著高于上覆水体。早期成岩过程是控制长江口沉积物孔隙水营养盐和Fe、Mn分布的主要因素。NH^4＋剖面暗示长江口近岸和远岸海域存在两类不同的生物地球化学过程。孔隙水Fe、Mn剖面暗示在河口环境中其是有机质降解的重要电子受体。在近岸海域MnO2可能是底部NH4^＋ -N移除的重要机制。长江口孔隙水中低磷酸盐与铁及沉积物中磷的形态有关。通量计算结果显示NH4^＋、NO3^-、PO4^3-、地SiO4、Fe和Mn向上覆水体扩散的通量分别为356—3074μmol／（m2·d）、-45．3～62．6μmol／（m2·d）、-0．3～1．7μmol／（m^2·d）、323—3172μmol／（m^2·d）、3．0～10．5μmol／（m^2·d）和35．7～439．5μmol／（m^2·d）。N、P、Si界面通量对上覆水体浮游生物所需营养盐的贡献分别为0．19％～1．65％、0．13％～0．14％和1．2％～12．2％,因此在考虑长江口区域浮游生物所需营养的来源时,沉积物-水界面营养盐扩散通量可以忽略。 相似文献
10.
The organic matter-rich Toolebuc Formation of eastern Australia was deposited in a Lower Cretaceous epicontinental sea. Parameters from biological marker studies indicate that the organic matter is immature to marginally mature for hydrocarbon generation. The occurrence of abundant coccoliths and the distribution of alkane biomarkers suggest that the organic matter (Type II) is largely of planktonic origin and only in the southeastern part of the depositional area can a terrestrial influence be discerned. Variations in kerogen composition can be attributed to the extent of the oxidation of the source materials and the degree of incorporation of sulphur. The atomic H/C ratios (c. 1.1) are remarkably constant for most of the Toolebuc Formation. Atomic O/C ratios vary from 0.1 and 0.4 and can be related both to depth and paleogeographic position. Kerogen sulphur contents range up to 7%, and the highest values occur in the most carbonate-rich sediments. Total sulphur (inorganic + organic) to carbon ratios in the sediments vary from 1 to <0.2 and are a function of paleogeographic position and lithology. Most of the sulphur in the sediments is in the form of pyrite, but the proportion of sulphur in organic form increases as the total sulphur content decreases. The evidence for oxidation of the organic matter and incorporation of sulphur into it during deposition suggests that bituminite, which is the dominant organic maceral in the Toolebuc Formation, was formed from an organic gel derived by decay of predominantly algal material. These data support a modified gyttja model (Kauffman, 1981) for the deposition of organic matter in the Toolebuc Formation. 相似文献
11.
潮白河是京津冀地区的重要河流。本研究以潮白河中游段为研究区,针对该区段沉积物有机质、氮磷污染程度不明的问题,通过对研究区130个采样点表层沉积物中有机质(OM)、总氮(TN)和总磷(TP)的测定,分析了表层沉积物中有机质和氮磷的分布特征及污染来源,将有机指数和有机氮污染指数评价法相结合开展污染及生态风险评价。结果表明:(1)潮白河中游表层沉积物中OM含量变化范围为0.17%~13.15%,平均含量为5.32%; TN的含量为0.005~1.028 g/kg,平均含量为0.192 g/kg;TP的含量为0.367~4.825 g/kg,平均含量为1.662 g/kg。(2)相关性分析表明,OM与TP、OM与TN均呈弱相关,而TN与TP呈强相关。这是因为TN和TP来源相近,主要来自外源,与OM来源有一定差异。根据TOC/TN特征分析,OM主要受藻类、浮游植物和非纤维束植物等影响。(3)有机指数评价结果显示,潮白河中游段表层沉积物监测点中60%为清洁,33.85%为较清洁,4.62%为尚清洁,1.54%为有机污染。有机污染点主要位于运潮减河入潮白河口和田贾庄排干渠入潮白河口。区域有机氮评价结果以清洁级别为主,整体较好。 相似文献
12.
Daniele Botelho de Souza Karina Scurupa Machado Sandro Froehner Cristóvão Fernandes Scapulatempo Tobias Bleninger 《Chemie der Erde / Geochemistry》2011,71(2):171-176
The geochemical composition of lake bed sediments of a tropical reservoir in Brazil have been investigated. The C, N, P composition showed almost no variation between the different sampling points. All samples contained inorganic phosphorus (IP) ranging from 52 to 70%. The Redfield ratios show that the lake is without significant anthropogenic inputs. Most of the organic matter is composed by higher plants decomposition revealed in the total organic carbon (TOC):nitrogen (N) ratio ranging from 15.4 to 57.2. Also, TOC:organic phosphorus (OP) ranged from 265.3 to 933.6, suggesting that most of the organic matter has terrestrial origin from wood plants. The ratios suggest that most organic matter is influenced by the terrestrial characteristics of the watershed. Furthermore, the relative abundance of n-alkane homologues in the sediments was investigated. All samples have been analyzed for the n-alkanes C8 to C40. The sediments were dominated by n-alkanes C25–C38. It is concluded that n-alkane in sediments mainly come from terrestrial plants, however there is a contribution of submerged aquatic plants, especially in those sites in deeper areas of the lake. On the basis of Paq index the n-alkanes in sediments comes from terrestrial plants, however there is a contribution from emerged/floating plants.The investigated lake seems to be considered as meso to eutrophic. Because of the relatively high primary productivity in the lakes, there is a substantial organic-matter flux to the sediments, which rapidly becomes anoxic. According to the pristine/phytane ratio the sediments represent an anoxic environment with values found between 0.38 and 1.72. 相似文献
13.
14.
Abundances of organic carbon, sulfur, and reactive iron in sediments of three upwelling environments (Peru, Oman and Benguela) suggest that organic carbon/reduced sulfur ratios (C/S-ratios) in this category of marine sediments deviate considerably from previously established empirical ratios in normal marine sediments. To clarify the discrepancies, we investigated those components of the diagenetic system that limit the formation of pyrite: sulfate concentrations and reduction rates in pore waters, availability of reactive iron, and the quantity and quality of organic matter. All three limitations are evident in our sample pools. The results suggest that C/S-ratios in recent and fossil marine sediments rich in organic matter may be unsuitable as paleoenvironmental indicators. 相似文献
15.
Federica Tamburini Sylvain HuonPhilipp Steinmann Francis E GroussetThierry Adatte Karl B Fllmi 《Geochimica et cosmochimica acta》2002,66(23):4069-4083
Reactive phosphorus undergoes diagenetic transformation once transferred into marine sediments. The degree of regeneration and redistribution of phosphorus depends on early diagenetic and environmental conditions, which may be linked to larger scale phenomena, such as bottom water circulation, water column ventilation, and organic carbon flux. Phosphorus phases of the <50-μm-sized fraction of deep-sea sediments from core SU 90-09 (North Atlantic, 43°31′N, 30°24′W, 3375 m below sea level) have been analyzed using a sequential extraction technique (SEDEX method) to reconstruct phosphorus geochemistry during Heinrich events 4 and 5. Comparison with Holocene samples from the same site indicates that postdeposition diagenetic transformation has not affected phosphorus distribution in the deep part of the sediments. Total and reactive phosphorus average 0.40 ± 0.04 mg/g and 0.30 ± 0.05 mg/g, respectively, and are comparable to values found in analog deep-sea environments in the North Atlantic. Detrital phosphorus, the phase linked to igneous- and metamorphic-derived material, sharply increases during Heinrich events and covaries with the ice-rafted debris record, whereas authigenic and Fe-bound phosphorus phases, both influenced by redox conditions, decrease or even disappear. These findings suggest that during the deposition of Heinrich layers (HLs), environmental parameters hampered the precipitation of these phases. Large freshwater discharges in relation to iceberg surges may have provoked a temporary stratification of the water column. Accordingly, dysaerobic conditions in the sediments may have fostered the loss of dissolved phosphorus from the sediments to the water column, in a direct and rapid response to the changed conditions. Decreasing trends in organic matter elemental ratios (total organic carbon/organic phosphorus) and Rock-Eval oxygen index values, along with the presence of partly authigenic dolomite and ankerite within HLs, also support this assumption. 相似文献
16.
云南星云湖中蓝铁矿结核的发现及环境意义 总被引：1，自引：0，他引：1
本文从矿物学、物理性质和化学组成等方面确定了首次在云南星云湖沉积物中发现的蓝铁矿结核.提供了蓝铁矿的X射线的峰值特征和红外光谱图;在讨论铁质和磷质来源及还原环境产生的基础上,提出了蓝铁矿的形成机理。认为蓝铁矿结核可以反映原始沉积环境,是-种内陆淡水湖泊的沉积标志,仅存在于淡水浅湖及湖湾沉积物中,反映-种浅湖及湖湾的低能环境。 相似文献
17.
Fifty-eight rock chips from fifteen samples of sedimentary rocks from the Ramah Group (approximately 1.9 Ga) in northeastern Labrador, Canada, were analyzed for major and minor elements, including C and S, to elucidate weathering processes on the Earth's surface about 1.9 Ga ago. The samples come from the Rowsell Harbour, Reddick Bight, and Nullataktok Formations. Two rock series, graywackes-gray shales of the Rowsell Harbour, Reddick Bight and Nullataktok Formations, and black shales of the Nullataktok Formation, are distinguishable on the basis of lithology, mineralogy, and major and trace element chemistry. The black shales show lower concentrations than the graywackes-gray shales in TiO2 (0.3-0.7 wt% vs. 0.7-1.8 wt%), Al2O3 (9.5-20.1 wt% vs. 13.0-25.0 wt%), and sigma Fe (<1 wt% vs. 3.8-13.9 wt% as FeO). Contents of Zr, Th, U, Nb, Ce, Y, Rb, Y, Co, and Ni are also lower in the black shales. The source rocks for the Ramah Group sediments were probably Archean gneisses with compositions similar to those in Labrador and western Greenland. The major element chemistry of source rocks for the Ramah Group sedimentary rocks was estimated from the Al2O3/TiO2 ratios of the sedimentary rocks and the relationship between the major element contents (e.g., SiO2 wt%) and Al2O3/TiO2 ratios of the Archean gneisses. This approach is justified, because the Al/Ti ratios of shales generally retain their source rock values; however, the Zr/Al, Zr/Ti, and Cr/Ni ratios fractionate during the transport of sediments. The measured SiO2 contents of shales in the Ramah Group are generally higher than the estimated SiO2 contents of source rocks by approximately 5 wt%. This correction may also have to be applied when estimating average crustal compositions from shales. Two provenances were recognized for the Ramah Group sediments. Provenance I was comprised mostly of rocks of bimodal compositions, one with SiO2 contents approximately 45 wt% and the other approximately 65 wt%, and was the source for most sedimentary rocks of the Ramah Group, except for black shales of the Nullataktok Formation. The black shales were apparently derived from Provenance II that was comprised mostly of felsic rocks with SiO2 contents approximately 65 wt%. Comparing the compositions of the Ramah Group sedimentary rocks and their source rocks, we have recognized that several major elements, especially Ca and Mg, were lost almost entirely from the source rocks during weathering and sedimentation. Sodium and potassium were also leached almost entirely during the weathering of the source rocks. However, significant amounts of Na were added to the black shales and K to all the rock types during diagenesis and/or regional metamorphism. The intensity of weathering of source rocks for the Ramah Group sediments was much higher than that of typical Phanerozoic sediments, possibly because of a higher PCO2 in the Proterozoic atmosphere. Compared to the source rock values, the Fe3+/Ti ratios of many of the graywackes and gray shales of the Ramah Group are higher, the Fe2+/Ti ratios are lower, and the sigma Fe/Ti ratios are the same. Such characteristics of the Fe geochemistry indicate that these sedimentary rocks are comprised of soils formed by weathering of source rocks under an oxygen-rich atmosphere. The atmosphere about 1.9 Ga was, therefore, oxygen rich. Typical black shales of Phanerozoic age exhibit positive correlations between the organic C contents and the concentrations of S, U, and Mo, because these elements are enriched in oxygenated seawater and are removed from seawater by organic matter in sediments. However, such correlations are not found in the Ramah Group sediments. Black shales of the Ramah Group contain 1.7-2.8 wt% organic C, but are extremely depleted in sigma Fe (<1 wt% as FeO), S (<0.3 wt%), U (approximately l ppm), Mo (<5 ppm), Ni (<2 ppm), and Co (approximately 0 ppm). This lack of correlation, however, does not imply that the approximately 1.9 Ga atmosphere-ocean system was anoxic. Depletion of these elements from the Ramah Group sediments may have occurred during diagenesis. 相似文献
18.
南四湖及主要入湖河流沉积物中磷的赋存形态研究 总被引：13，自引：0，他引：13
应用沉积物磷形态SMT提取方法,分析了南四湖及主要入湖河流丰水季节表层沉积物、独山湖及微山湖区沉积岩芯中磷的含量及形态组成变化,研究了磷的埋藏演化过程与人为污染特征.结果表明,老运河表层沉积物中磷的含量最高,为13068.3 mg/kg,以OP及NaOH-P为主,其富集系数分别为6.5和9.0,主要是与来自济宁市的废水污染有关.其余表层沉积物以HCl-P为主;受人为污染的影响,NaOH-P、OP产生一定程度的富集,其富集系数分别为1.0.3.7、1.3～6.0;部分沉积物中高含量的有机质加重了OP的富集.独山湖及微山湖沉积岩芯中以HCl-P和OP为主;20世纪60年代末期以来,随着湖泊生产力的提高及早期成岩过程中有机质的矿化分解,独山湖及微山湖沉积岩芯中TOC含量自下而上呈指数增加,这也导致了沉积物中OP的增加;独山湖及微山湖沉积岩芯6～0 cm和5～0 cm较高的OP及NaOH-P含量,指示了20世纪80年代中期以来磷的人为污染过程. 相似文献
19.
A. I. Brusnitsyn V. N. Kuleshov E. N. Perova A. N. Zaitsev 《Lithology and Mineral Resources》2017,52(3):192-213
The paper presents the results of study of ferromanganese carbonate rocks in the Sob area (Polar Urals), which is located between the Rai-Iz massif and the Seida–Labytnangi Railway branch. These rocks represent low-metamorphosed sedimentary rocks confined to the Devonian carbonaceous siliceous and clayey–siliceous shales. In terms of ratio of the major minerals, ferromanganese rocks can be divided into three varieties composed of the following minerals: (1) siderite, rhodochrosite, chamosite, quartz, ± kutnahorite, ± calcite, ± magnetite, ± pyrite, ± clinochlore, ± stilpnomelane; (2) spessartite, rhodochrosite, and quartz, ± hematite, ± chamosite; (3) rhodochrosite, spessartite, pyroxmanite, quartz ± tephroite, ± fridelite, ± clinochlore, ± pyrophanite, ± pyrite. In all varieties, the major concentrators of Mn and Fe are carbonates (rhodochrosite, siderite, kutnahorite, Mn-calcite) and chlorite group minerals (clinochlore, chamosite). The chemical composition of rocks is dominated by Si, Fe, Mn, carbon dioxide, and water (L.O.I.): total SiO2 + Fe2O 3 tot + MnO + L.O.I. = 85.6?98.4 wt %. The content of Fe and Mn varies from 9.3 to 55.6 wt % (Fe2O 3 tot + MnO). The Mn/Fe ratio varies from 0.2 to 55.3. In terms of the aluminum module AlM = Al/(Al + Mn + Fe), the major portion of studied samples corresponds to metalliferous sediments. The δ13Ccarb range (–30.4 to–11.9‰ PDB) corresponds to authigenic carbonates formed with carbon dioxide released during the microbial oxidation of organic matter in sediments at the dia- and/or catagenetic stage. Ferromanganese sediments were likely deposited in relatively closed seafloor zones (basin-traps) characterized by periodic stagnation. Fe and Mn could be delivered from various sources: input by diverse hydrothermal solutions, silt waters in the course of diagenesis, river discharges, and others. The diagenetic delivery of metals seems to be most plausible. Mn was concentrated during the stagnation of bottom water in basin-traps. Interruption of stagnation promoted the precipitation of Mn. The presence of organic matter fostered a reductive pattern of postsedimentary transformations of metalliferous sediments. Fe and Mn were accumulated initially in the oxide form. During the diagenesis, manganese and iron oxides reacted with organic matter to make up carbonates. Relative to manganese carbonates, iron carbonates were formed under more reductive settings and higher concentrations of carbon dioxide in the interstitial solution. Crystallization of manganese and iron silicates began already at early stages of lithogenesis and ended during the regional metamorphism of metalliferous sediments. 相似文献
20.
Organic matter and nutrients in an altered subtropical marsh system,Chiricahueto, NW Mexico 总被引：2，自引：0，他引：2
Seven sediment push-cores were extracted from Chiricahueto, a marsh affected by urban, industrial and agricultural wastes. Concentrations of total phosphorus (300-1,620 µg g-1), organic carbon (4-39 mg g-1) and total nitrogen (0.5-4.5 mg g-1) in the sediments showed an exponential decrease with depth, related to the decomposition of organic matter (OM). Between 20 and 40% of OM initially deposited is degraded at the sediment-water interface under oxic conditions. Another fraction (40-60%) of non-refractory OM is decomposed within the sediments by oxidants other than oxygen. Likewise, the preservation of OM (<20%) was estimated as burial concentrations of C, N and P linked to organic compounds. The C/N ratios, '13C and '15N suggested that the major source of OM to the sediments derives from marine phytoplankton. The allochthonous sources of OM were overprinted by the high flux of marine autochthonous OM. However, an indirect terrestrial influence is recognised, in which high nutrient load derived from agricultural, domestic and industrial activities promoted high productivity. 相似文献