共查询到19条相似文献，搜索用时 93 毫秒
1.
氧化还原条件对红枫湖沉积物磷释放影响的微尺度分析 总被引：7，自引：0，他引：7
选取贵州红枫湖为研究对象,在实验室条件下模拟了自然、好氧和厌氧条件下沉积物内源磷的释放过程,联合应用微电极技术和沉积物磷形态分析对沉积物—水界面开展了微尺度观测与研究.结果表明,厌氧条件下红枫湖沉积物总磷含量显著降低,且主要是NaOH提取态磷(NaOH-P)和残渣态磷(rest-P)含量降低所致,厌氧条件下沉积物孔隙水中磷酸盐浓度明显升高,而好氧条件下沉积物孔隙水磷酸盐浓度显著降低,反映厌氧条件显著促进了红枫湖沉积物磷释放.厌氧条件下沉积物内部溶解氧浓度下降、硫还原活动增强可能是导致NaOH-P释放的主要原因.O_2浓度的降低加速了沉积物还原作用并产生大量H2S,进而与二价铁离子形成硫化亚铁沉淀,最终导致NaOH-P(Fe-P)释放到孔隙水中.好氧条件向厌氧条件的转换可通过改变沉积物内部pH值分布和微生物活动促使rest-P释放:厌氧条件下,厌氧微生物不仅可以消耗硫酸根产生H_2S,导致pH值降低,还可消耗有机质,将有机磷转变为无机磷.上述研究结果表明,沉积物—水界面氧化还原环境可影响沉积物氧渗透深度、pH值分布、微生物活动、硫循环以及有机质降解过程,进而控制沉积物磷的形态转化与释放.联合应用微电极技术和沉积物磷形态分析对湖泊沉积物—水界面开展微尺度观测研究是揭示沉积物内源磷释放机制与控制因素的有效途径. 相似文献
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湖泊沉积物有机质碳同位素因常被用于识别沉积物中有机质来源或流域植被信息而逐渐成为一个常规代用指标,但当沉积物中有机质含量变化显著、赋存状态不同时,采用统一分析方法(全样或某一粒级组分)测试的结果在不同含量或赋存状态时是否会产生偏差,目前没有详细的研究进行评价.利用嘎顺诺尔湖泊沉积物,采用全样品、细颗粒组分(过120目筛和360目筛),分别进行有机质含量和同位素分析,评价选择不同粒级样品因有机质赋存状态不同对有机碳同位素分析结果的影响.结果显示,不同组分的烧失量或元素分析仪方法测得的有机质含量变化趋势相同,但不同组分的有机碳同位素结果出现差异:全样的有机碳同位素值存在较大波动,随着过筛孔径变小,δ13Corg值波动减小,且过360目筛的细颗粒组分的碳同位素值较全样或过120目筛后组分的δ13Corg值偏负.这一差异与有机质组分赋存的颗粒范围有关.对比认为过360目筛的细颗粒组分更有利于充分反应,且可获得较为准确的同位素值.因此,在进行不同湖泊沉积物δ13Corg值对比时,应注意研究使用样品的前处理方式,相同处理方式下的结果更具有可比性.该研究结果对于湖泊沉积物有机质碳同位素分析具有参考意义. 相似文献
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磷是地表水体中的关键性营养盐,在水生生态系统的物质循环与能量流动方面发挥着重要作用,研究水体中磷的来源、转化与归趋对于了解水环境的演变过程与科学保护具有重要意义.近年来,磷酸盐氧同位素(δ18 O P)技术已逐渐应用于淡水环境中磷的来源示踪与生物地球化学循环研究,其样品前处理主要沿用海水方法体系.相比而言,淡水样品中PO 3-4浓度通常较低,有机质和干扰离子含量却较高,复杂的样品前处理过程极大地制约了δ18 O P分析在淡水环境体系的广泛应用.为此,本研究针对现有海水样品δ18 O P前处理方法在地表淡水环境的适用性加以检验,并进行了三点优化改进:①将MAGIC沉淀步骤使用的MgCl 2替换为Mg(NO 3)2,避免了Cl-的干扰,减少AgCl杂质的生成;②调节生成Ag3PO4溶液pH值为8.0,保证Ag3PO4沉淀快速完全;③对Ag3PO4沉淀过程采用避光处理,降低了AgNO 3及Ag3PO4可能的光解影响,提高了Ag3PO4的纯度,使δ18 O P的测试结果更为准确.本改进方法为后续利用δ18 O P技术深入探究淡水环境中磷的生物地球化学循环与生态环境效应提供了有益的方法借鉴. 相似文献
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富营养化湖泊沉积物有机质矿化过程中碳、氮、磷的迁移特征 总被引：7，自引：2，他引：5
采用室内培养的方法,以富营养化湖泊太湖为例,研究了沉积物有机质矿化过程中碳、氮、磷的迁移特征.结果表明,在沉积物中的有机质矿化过程中,碳以溶解性无机碳释放至水中,同时以CH4和CO2形式释放至大气中,培养结束时,CH4和CO2累积排放含量分别为1492.21和498.96 mg/g(dw),其中CH4占气态碳的89.16%(以C质量计);此外,大量的氮、磷营养盐释放至上覆水体,水中总氮、总磷和铵态氮的最高浓度分别是初始浓度的62.16、28.16和139.45倍,而硝态氮浓度在整个培养过程中逐渐下降,培养末期浓度是初期的0.21倍;厌氧条件下,沉积物有机质的矿化,不仅可以生成大量的CH4、CO2气体,还能够促使沉积物中铵态氮和磷的释放;而沉积物有机质矿化释放的碳、氮、磷营养元素又能加剧湖泊富营养化程度,促进湖泊水体的初级生产力,从而增加湖泊沉积物有机质输入.这样的循环方式可能是湖泊富营养化自维持的重要机制之一. 相似文献
6.
云南程海沉积物碳酸盐来源辨识 总被引：8，自引：2，他引：6
碳酸盐是湖泊沉积物的组成部分,其碳、氧同位素组成是恢复湖区古气候/古环境的有效代用指标.沉积物碳酸盐包括物源区带来的外源碳酸盐和湖泊内生沉淀产生的自生碳酸盐,其中只有自生碳酸盐才具有古气候指示意义.故沉积物碳酸盐来源辨识是开展碳酸盐古环境记录研究的基础和前提.通过多种方法的综合判别,证明了程海沉积物碳酸盐主要是自生碳酸盐,为开展碳酸盐记录研究提供了可靠依据.程海是开展碳酸盐碳氧同位素与古气候研究的理想场所,尤其值得深入研究. 相似文献
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博斯腾湖表层沉积物无机碳及其稳定同位素空间异质性 总被引：4，自引：2，他引：2
2012年8月,在新疆博斯腾湖13个站点进行表层沉积物采集,分析无机碳及其碳、氧稳定同位素的含量和空间分布特征,探讨该湖表层沉积物无机碳(TIC)的空间变化影响因素.结果表明:2012年,博斯腾湖表层沉积物TIC含量平均值为5.5%,变幅为3.8%~9.8%,而δ13Ccarb和δ18Ocarb平均值分别为0.71‰和-4.4‰,范围为-0.23‰~2.27‰和-5.53‰~-2.55‰.从空间来看,湖泊北岸TIC值明显高于南岸,最高值出现在湖泊西北部的黄水沟水域,而河口区和湖心区最低.总体上,博斯腾湖表层沉积物TIC主要是湖泊自生的,其空间分布主要受开都河、黄水沟等入湖河水的影响,导致水体矿化度和营养盐的空间差异,进而影响了碳酸盐的析出与沉淀.另外,湖泊局部的水动力条件也影响TIC的保存与分布.δ13Ccarb与δ18Ocarb的极显著正相关说明近几年博斯腾湖封闭程度较好,尤其是东部大湖区,属于封闭环境碳酸盐沉淀. 相似文献
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太湖梅梁湾富营养化过程的同位素地球化学证据 总被引：4，自引：0，他引：4
以浅水湖泊太湖为研究对象,通过湖泊水体、水生生物同位素以及相应湖泊水体营养指标的比较分析,并根据梅梁湾钻孔沉积物TN,TP,TOC,C/N,δ15N,δ13C等多项指标记录,恢复了湖泊富营养化过程.研究结果表明,不同湖区植物碳、氮同位素值和水体NH4+的δ15N值变化反映了植物组成和营养水平的差异.梅梁湾水体NH4+的δ15N和水环境参数不同月份的变化反映了外部营养载荷的输入对湖泊环境有明显的影响.1950～1990年湖泊沉积物有机质碳、氮同位素同步变化的趋势说明湖泊初级生产力的增长和湖泊逐渐富营养化的过程,而1990年之后二者之间反相关关系的出现表明在富营养条件下,大量浮游植物生长对富15N的无机氮的吸收及表层沉积物有机质分解和反硝化作用,代表湖泊富营养化加剧.以同位素示踪,并结合元素地球化学指标变化,将太湖梅梁湾富营养化过程分为三阶段,以20世纪50年代和20世纪90年代为营养状态的转换时段,揭示了人类活动不断加强的影响,与近50年来的湖泊环境监测结果一致. 相似文献
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湖泊现代沉积物碳环境记录研究 总被引：37，自引：3，他引：37
通过对云南程海现代沉积物的精细采样和分析, 研究了湖泊沉积物中有机碳与无机碳含量阶段性的正相关和负相关变化. 结果表明, 温度及其引起的相关变化是控制沉积物无机碳含量、碳酸盐δ 13C和有机碳含量变化关系的主要因素. 当温度及其引起的光合作用强度变化对湖泊自生碳酸钙沉淀起主导作用时, 沉积物有机碳含量与无机碳含量及碳酸盐δ 13C呈正相关变化; 当温度及其引起的蒸发速率等其他物理化学因素变化对湖泊自生碳酸钙沉淀起主导作用时, 沉积物有机碳含量与无机碳含量及碳酸盐δ 13C呈负相关变化. 程海沉积物无机碳含量和碳酸盐δ 13C是湖区气候冷暖变化的良好代用指标. 相似文献
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Phosphate behaviour in natural estuarine systems can be studied by performing field measurements and by undertaking laboratory simulation experiments. Thus, in this paper we describe the use of a dynamic automated estuarine simulator to characterize the geochemical reactivity of phosphate in varying salinity gradients in order to study possible mechanisms of phosphate removal from the dissolved phase (e.g. formation of some kind of apatite) and how changes in pH and salinity values influence this removal. Six laboratory assays, representing various salinity and pH gradients (average pH values between 7 and 8), were carried out. The geochemical equilibrium model MINTEQA2 was employed to characterize removal of phosphate. Among the minerals from which dissolved phosphate can originate, it seems that hydroxyapatite is by far the mineral that shows the greatest saturation indexes in the experiments. Thus, there is evidence that a type of calcium phosphate (hydroxyapatite) is involved in phosphate removal in the assays. Phosphate removal by Ca2+ occurs sharply at salinity values of 1–2, whereas by Fe3+ it is relatively gradual, at least until a salinity value of 7. Copyright © 2006 John Wiley & Sons, Ltd. 相似文献
12.
ZHANG Lu ZHU Guangwei LUO Liancong GAO Guang ZHANG Yunlin QIN Boqiang FAN Chengxin 《中国科学D辑(英文版)》2006,49(Z1)
Variation of wind speed and the physico-chemical parameters, such as dissolved phosphate, ferrous and manganese in lake water were observed on site. Together with the chemistry analysis and simulated experiment in lab, the change of phosphate concentration in lake water was analyzed. The variation of ferrous/phosphate ratio explained that along with the enhancement of wind-wave effect and the oxidation ability of lake water, the effects of co-precipitation and removal of dissolved phosphate and iron in the lake water were reinforced. The ferrous/phosphate ratio in pore water was less than 2.0, demonstrating that the dissolved phosphate can be released into the overlying water. But, in the lake water, the stability of phosphate was controlled by the water dynamics. The phosphate release experiment showed that molecular release was only part of the whole and the direct discharge of phosphate in the pore water was also a part. The mineralization and biological process of suspended particulates in the water may be another important reason for the whole phosphate loadings. 相似文献
13.
Accurate crystal structure determination of complex phosphate Mg-fillowite.—Na2Ca(Mn4Mg2Fe)7[PO4]6 has been finished. Mg-fillowite occurs in muscovite-pegmatite in the Altay area, Xinjiang, China. It is of the trigonal lattice,
with space group R-3, unit cell a=1.5143(3)nm, c=4.3191(2) nm, V=8.5736 nm3, Z = 18. The R-factor of the determination accuracy is R (I<2 σ(I)) = 0.0776. The cationic polyhedra consist of two kinds of structural units: compound column and screw column. In three-dimensional
space, they are linked with each other through corner sharing or edge sharing to build the entire structure. There are 45
atoms in an asymmetric unit and 720 atoms in a unit cell. In terms of types and connection manners of the coordination polyhedra,
the degree of complicity is rarely seen in all mineral crystal structures. Study of such a structure is significant for the
classification of phosphate and the building rule of coordination polyhedra in a complex crystal structure. 相似文献
14.
This study investigates the influence of Ca2+ and Mg2+ on the removal of F? by magnesium potassium phosphate (MPP) from water. The kinetic experiments reveal that the F? concentration decreased from 3.5 to 3.31 mg L?1 in a single (F?) system and to 1.45 mg L?1 in a ternary system (F?, Ca2+, and Mg2+) after 1 min, respectively. Thus, the F? removal efficiencies are found to increase by about 53% with the co‐active effect of Ca2+ and Mg2+ in the solution. Moreover, Ca2+ and Mg2+ are almost completely removed in the F?, Ca2+, and Mg2+ system. According to the pseudo‐first‐order modeling, the rate constants k for F?, Ca2+, and Mg2+ are 0.00348, 0.0106, and 0.0159 min?1 respectively; thus, Mg2+ > Ca2+ > F?. In the ternary system, the removal efficiencies are 53.29–66.03% for F?, 99.99–100% for Ca2+, and 87.21–95.19% for Mg2+ with initial pH 5–10. The removal efficiencies of F? increases with increases in initial concentrations of F?, Ca2+, and Mg2+. The removal of F? is governed by two routes: 1) adsorption by electrostatic interactions and outer sphere surface complexation; 2) co‐precipitation with Ca3(PO4)2, CaHPO4, Mg3(PO4)2, and Mg(OH)2. 相似文献
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Sediment diffusive fluxes of Fe,Mn, and P in a eutrophic lake: Contribution from lateral vs bottom sediments 总被引：3，自引：0，他引：3
Nelson Belzile Jaime Pizarro Montserrat Filella Jacques Buffle 《Aquatic Sciences - Research Across Boundaries》1996,58(4):327-354
Water column data and porewater profiles are used to study the chemical evolution with time and with depth of a eutrophic lake. By using different approaches, diffusion fluxes for dissolved iron, manganese and phosphate are calculated and used to describe the processes occurring at the sediment-water interface as well as in the hypolimnion of the lake. These data are used in the elaboration of a qualitative model to describe the chemical behaviour of the sedimentary interface of an anoxic lake with emphasis on the Fe/P/S system. Acorona model is proposed to explain the evolution with time of the diffusion process by estimating the relative contribution of bottom and lateral sediment surfaces to the total fluxes of dissolved elements diffusing from the sediment to the overlying water. As the hypolimnion becomes more anoxic, it has been observed that lateral sediment surfaces (16 to 10 meters in depth) represents a larger supplier of diffusing dissolved components than the bottom sediment portion (bottom to 18 meters). 相似文献
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The deterioration of sediments is a serious environmental problem. Controlling nutrient release fluxes from sediments is important to alleviating eutrophication and to reducing terrigenous nutrient loads. The purpose of this study was to evaluate the phosphate removal performance of granulated coal ash (GCA) from seawater, which is produced from coal thermal electric power generation. Batch experiments were carried out to investigate the removal kinetics of phosphate from seawater under both oxic and anoxic conditions. Phosphate was removed well from seawater under both oxic and anoxic conditions. The adsorption isotherm for phosphate revealed that GCA could remove phosphate effectively from seawater above a concentration of 1.7 μmol L−1. GCA can reduce the concentration of phosphate in seawater effectively under anoxic conditions where iron type adsorbents cannot be applied. Therefore, GCA could potentially be used to adsorb phosphate in the organically-enriched sediment, which generally occurs under highly reductive conditions. 相似文献
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《Geofísica Internacional》2014,53(4):399-409
In the Sidi Chennane basin exploitation inclusions of sterile hardpan—so-called “derangements” — are hard to detect and interfere with phosphate extraction. A Schlumberger resistivity survey over an area of 50 hectares was carried out. The Savitzky-Golay filtering method was used as a tool for denoising the data.Savitzky-Golay (S-G) filters are one of the filters which can smoothen out the signal without much destroying its original properties. Despite their exceptional features, they were rarely used so far in the geophysical signal processing. The aim of this paper is the investigation of their properties in detail from the geoelectrical signal processing aspect. The experimental results indicate that S-G filter is better for denoising geoelectrical signal. Models of the geology were successfully obtained from Savitzky-Golay filtering method, which help mapping the phosphate deposit inclusions and the estimations of phosphate reserves were improved and better constrained. 相似文献
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利用薄膜扩散平衡技术分析沉积物间隙水溶解态反应性磷 总被引：5，自引：0，他引：5
沉积物间隙水溶解态反应性磷(SRP)是反映沉积物磷地球化学特征的敏感指标,对其高分辨率获取一直是难点.基于薄膜扩散平衡(DET)原理,以琼脂糖为原料制备薄膜,通过平衡、切片、提取、测定等步骤,获得溶解态反应性磷的含量信息.实验确定薄膜在磷溶液中的平衡时间为24h,通过0.25mol/L硝酸提取16h可将薄膜萃取的磷提取完全.利用DET技术对不同沉积物间隙水SRP进行了分析,与实际浓度的差异在±5%以内;对沉积物剖面的分析结果与Rhizon、微型Peeper等采样技术基本一致,垂直分辨率可达到3mm左右.利用DET技术对太湖草型和藻型湖区沉积物间隙水SRP进行丁分析,发现草型湖区间隙水剖面SRP呈峰形分布,且横向空间分异明显;藻型湖区间隙水SRP随沉积深度的增加呈升高趋势,扩散梯度随水温升高而增强. 相似文献