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滇池福保湾沉积物磷的形态及其与间隙水磷的关系 总被引:10,自引:1,他引:10
研究了滇池福保湾沉积物中磷的地球化学形态及间隙水中PO43--P含量的垂向分布特征.福保湾沉积物磷形态空间差异大,河口区TP高达(5630.59±424.25)mg/kg,东西沿岸区TP只有200-300mg/kg,无机磷(I-P)是TP的主要部分,占TP的55%-74%,铁/铝结合态磷(Fe/Al-P)是I-P的主要组成部分,约占I-P的90%,不稳定性磷∞P)含量很低,只占TP含量的0.5%.福保湾沉积物具有极高的Fe/Al-P含量,说明湾内具有很高的内源磷负荷,这与福保湾水体严重富营养化和藻类暴发关系密切.湖湾沉积磷的垂向分布规律较复杂,但基本上是随深度增加而减小,说明福保湾周边区域近几年人类活动作用加强,褐保湾污染有加重的趋势.在湾内不同区域应用Peeper(渗吸膜式)技术,获得了间隙水中PO43--P的垂向分布特征,PO43--P浓度自上覆水向下层间隙水呈先升后降,反映它们有自间隙水向上覆水扩散的趋势.福保湾间隙水PO43--P浓度同沉积物L-P含量具有显著正相关性(α=0.05),但Fe/Al-P、Ca-P、org-P和TP含量未发现有明显的相关关系. 相似文献
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滇池沉水植物生长过程对间隙水氮、磷时空变化的影响 总被引:4,自引:0,他引:4
2015年6-10月通过原位采集滇池沉水植物分布区和无植物对照区柱状沉积物间隙水,分析其溶解性总氮(DTN)和溶解性总磷(DTP)、溶解性无机氮(DIN)和溶解性无机磷(DIP)及溶解性有机氮(DON)和溶解性有机磷(DOP)浓度的时空变化,探讨沉水植物分布对间隙水氮、磷浓度、形态贡献及氮磷比的影响.结果表明:滇池沉水植物生长过程显著影响间隙水氮、磷浓度.与无植物对照区相比,沉水植物生长过程对间隙水氮浓度的削减主要发生在6、8月,而对间隙水磷浓度的削减主要发生在7月,反映了沉水植物对氮、磷两种元素的生物地球化学循环作用机制不同;间隙水氮形态贡献受季节性影响较大,6-7月以DON贡献为主,沉水植物分布区和无植物对照区分别达到61%和84%;而8-10月以DIN贡献为主,沉水植物分布区和无植物对照区分别为76%和75%;沉水植物分布区磷形态贡献随季节波动变化,沉水植物分布区以DOP贡献为主(63%),无植物对照区以DIP贡献为主(62%);沉水植物生长对沉积物间隙水各形态氮磷比影响显著.沉水植物生长显著增加间隙水DTN/DTP比,尤其是DIN/DIP比,相反降低DON/DOP比.沉水植物对间隙水氮、磷吸收及转化过程改变了沉积物氮、磷释放机制,从而影响上覆水氮、磷组成及氮磷比,很可能会影响到浮游植物生长及藻类水华过程,这对于湖泊水质管理具有重要意义. 相似文献
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滇池水-沉积物界面磷形态分布及潜在释放特征 总被引:11,自引:3,他引:11
通过现场调查和室内模拟实验,对滇池35个上覆水-沉积物磷的分布特征以及沉积物中磷释放动力学特征进行研究,结果表明:滇池表层沉积物中不同形态磷含量表现为:有机磷(OP)(1482.49±1156.82 mg/kg)钙结合态磷(Ca-P)(865.54±558.40 mg/kg)金属氧化物结合态磷(Al-P)(463.77±662.18 mg/kg)残渣态磷(Res-P)(218.52±83.11 mg/kg)可还原态磷(Fe-P)(128.13±101.56 mg/kg)弱吸附态磷(NH4Cl-P)(2.26±3.05 mg/kg);滇池上覆水草海总磷浓度处于劣Ⅳ类水平,外海不同湖区总磷浓度介于Ⅳ~Ⅴ类之间;滇池水体中的磷以颗粒态磷含量最高;滇池表层沉积物中磷的释放是由快反应和慢反应两部分组成.释放过程主要发生在前8 h内;不同区域沉积物磷的最大释放速率、最大释放量、磷的释放潜力平均值均表现为:草海外海北部外海南部湖心区;滇池表层沉积物中磷的释放主要由NH4Cl-P、Fe-P、Al-P和OP进行,其中,NH4Cl-P和Fe-P所占比重较大;磷的释放与上覆水中溶解性总磷、溶解态无机磷和溶解态有机磷呈显著正相关,预示着上覆水中磷的迁移转化更多地受到水-沉积物界面浓度梯度的控制,进一步说明不能以总磷含量来评价湖泊磷素释放的状况,需与磷形态及分布特征相结合进行分析. 相似文献
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湖泊沉积物的重金属污染防治一直是环境领域的热点问题.本研究采用氨基生物炭作为覆盖材料,利用梯度扩散薄膜技术(DGT),研究了上覆水不同pH及水流扰动条件下Cu(Ⅱ)、Pb(Ⅱ)在沉积物-水界面间的原位释放特征,以及氨基生物炭对湖泊沉积物重金属污染的原位修复效果.研究结果表明,在0r/min或100r/min水动力条件下,可移动态重金属离子有不断由沉积物向其他介质扩散的趋势,1.81kg/m2的氨基生物炭覆盖强度可降低Cu(Ⅱ)、Pb(Ⅱ)释放通量达89%以上,有效减小了水环境中重金属的潜在生态风险.在pH=5的酸性及pH=9的碱性水环境中原位修复效果较差,水体中大量的H+或络合物均会削弱氨基生物炭对重金属离子的吸附,当上覆水在pH=7的中性条件时原位修复效果最佳.100r/min水流扰动下的上覆水Cu(Ⅱ)、Pb(Ⅱ)含量在释放平衡时较0r/min条件下高出0.036~0.096μg/mL,说明高强度的水流扰动易造成覆盖材料的扬起和浮动,导致覆盖材料与重金属发生解吸. 相似文献
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鄱阳湖沉积物和水界面磷的交换通量 总被引:6,自引:0,他引:6
采用扩散模型法与实验培养法对鄱阳湖沉积物和水界面间可溶性总磷和可溶性磷酸盐的界面交换过程进行研究,并探讨了其影响因素.结果表明,利用2种方法得到鄱阳湖各站点可溶性总磷和可溶性磷酸盐在沉积物与水界面间的交换方向不完全相同,大部分站点沉积物是磷的源,其中,利用扩散模型法估算的可溶性总磷和可溶性磷酸盐平均扩散通量分别为0.052和0.047 mg/(m~2·d),而实验培养法测得可溶性总磷和可溶性磷酸盐的平均交换通量则分别为0.25和0.24 mg/(m~2·d),且各站点利用扩散模型法测得磷的交换通量均小于实验培养法的计算结果.此外,上覆水溶解氧浓度及水体温度对可溶性总磷和可溶性磷酸盐的交换过程均具有一定的影响,表现为温度越高,溶解氧浓度越小,可溶性总磷和可溶性磷酸盐的交换越强烈. 相似文献
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沉水植物生长对沉积物间隙水中的氮磷分布及界面释放的影响 总被引:14,自引:2,他引:14
采集未破坏沉积物结构的柱状沉积物样品,通过室内41 d的培养实验,研究了沉水植物生长过程对间隙水中NH_4~ -N和PO_4~(3-)-P的浓度的动态影响,分析了沉水植物生物量与沉积物中氮磷释放通量的对应关系.结果表明:随沉水植物生长和生物量增加,上部0-5 cm沉积物垂向各层间隙水中NH_4~ -N含量呈逐步降低,表现出沉积物-水界面氮的释放通量与沉水植物生物量存在负相关性;而间隙水PO_4~(3 )-P含量则随沉水植物生长呈单峰型变化,磷释放通量与生物量相关性不明显.初步反映沉水植物在沉积物的生长过程中对氮磷吸收的生物地球化学机制是不同的. 相似文献
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太湖不同营养水平湖区沉积物磷形态与生物可利用磷的分布及相互关系 总被引:30,自引:1,他引:30
采用EDTA螯合剂法和不同的化学提取法,研究了太湖3个不同营养水平湖区中8个位点表层沉积物总磷、各组分磷及生物可利用磷的含量分布,探讨了太湖不同营养水平湖区表层沉积物的释磷潜力和生物可利用磷的来源.结果表明,太湖不同营养水平湖区表层沉积物总磷、无机磷和生物可利用磷含量分布差异较大,且与各湖的营养水平相一致.有机磷含量与有机质和含水率显著相关;沉积物中Fe-P和Ca-P对生物可利用磷的贡献较大,这部分磷具有较大的潜在释放风险. 相似文献
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[专稿]湖泊沉积物-水界面研究进展与展望 总被引:2,自引:0,他引:2
湖泊沉积物-水界面是以水层/沉积层物相为基础、具有一定立体尺度的交接面,界面上所发生的由生物积极参与的物理、化学和生物学微小反应和环境变化,都会对界面附近物质的状态和迁移转化行为产生着复杂影响.本文首先回顾了沉积物-水界面研究100多年来的发展历程及国内外近20年发展.然后系统介绍了国际上对沉积物-水界面的物理尺度与结构的宏观和微观认识;重点综述了沉积物间隙水的取样、物化性质的多维测定与结构表征、过程的静态和动态模拟等湖泊沉积物-水界面研究技术与方法;分析和展示了氮磷等营养物、重金属和持久性有机污染物在湖泊沉积物-水界面迁移转化过程的研究进展;总结和归纳了在沉积物-水界面过程的模型研究、沉积物-水界面物质交换的定量化、界面过程与湖泊生态环境灾害关系等模型与过程效应方面的研究成果.最后对沉积物-水界面信息获取技术的研发方向、界面物质交换定量化研究的关注点,以及加强模型的应用和构建等方面进行了展望. 相似文献
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长江中下游典型浅水湖泊沉积物水界面磷与铁的耦合关系 总被引:6,自引:3,他引:6
目前普遍认为磷铁耦合关系是P迁移的主要机制,但大部分研究结果并未提供直接的原位证据.为了探索沉积物剖面磷(P)与铁(Fe)的耦合关系,利用Zr O-Chelex薄膜扩散梯度技术(ZrO-Chelex DGT),分别对太湖、巢湖、鄱阳湖和洞庭湖4个浅水湖泊沉积物有效态Fe和P进行高分辨采样和分析.结果表明,不同湖区有效态Fe和P浓度在沉积物-水界面处开始增加,之后波动变化,垂向异质性较强,但两者浓度变化同步.有效态P和Fe浓度的相关分析结果证明两者浓度具有显著的线性相关.室内厌氧培养实验进一步表明,Fe~(3+)的还原性促使Fe~(2+)与铁结合态磷的释放,促使DGT有效态P与Fe同步变化.该结果表明沉积物P的二次迁移和释放受Fe氧化还原过程的控制,为铁磷耦合关系提供了直接证据. 相似文献
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Measurement of soluble reactive phosphorus concentration profiles and fluxes in river-bed sediments using DET gel probes 总被引:3,自引:0,他引:3
Helen P. Jarvie Robert J.G. Mortimer Elizabeth J. Palmer-Felgate Katherine St. Quinton Sarah A. Harman Patricia Carbo 《Journal of Hydrology》2008,350(3-4):261-273
DET (diffusive equilibrium in thin films) gel probes were used for sampling river-bed sediment porewaters, to characterise in situ soluble reactive phosphorus (SRP) concentration profiles and fluxes. DET probes were deployed in three contrasting rural streams: (1) a headwater ‘pristine’ stream, with minimal P inputs from low intensity grassland and no point sources, (2) an intensively cultivated arable catchment, and (3) a stream subject to high P loadings from sewage effluent and intensive arable farming. The DET results showed highly enriched porewater SRP concentrations of between ca. 400 and 5000 μg-P l−1 in the sewage-impacted stream. In contrast, the arable and pristine streams had porewater SRP concentrations <70 μg-P l−1 and <20 μg-P l−1, respectively. Porewater SRP concentration profiles in both the sewage-impacted and arable-impacted streams showed well-defined vertical structure, indicating internal sources and sinks of SRP within the sediment. However, there was little variability in porewater SRP concentrations in the pristine stream. The DET porewater profiles indicated net diffusion of SRP (a) from the overlying river water into the surface sediment and (b) from subsurface sediment upwards towards the sediment–water interface. A mass balance for the sewage-impacted site showed that the influx of SRP into the surface sediments from the overlying river water was small (ca. 1% of the daily river SRP load). The DET results indicated that, in the arable and sewage-impacted streams, the surface ‘cap’ of fine sediment may play an important role in inhibiting upward movement of SRP from subsurface porewaters into the overlying river water, under steady-state, low-flow conditions. 相似文献
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Based on the research into the physical-chemical properties and distribution of sediments and the characteristics of pore water in sediments of Miyun reservoir, the release flux of the total phosphorus (TP) from sediments is estimated by simulating deposit environment of reservoir bottom in laboratory. They are 0.018 mg·cm-2·d-1 and 0.821 mg·cm-2·d-1 at 2℃ and 8℃ respectively. The gross TP released in a year is 11.34t. As a contrast, the pore water diffusion simulation method is used to measure gross TP released and gains 11.56t. The two results are relatively close and prove that experiment simulation has some reliability. On the basis of experiments, some conclusions can be drawn: (1) Endogenous phosphorus from sediments accounts for 27.9 percent of the TP entering the reservoir, and it cannot be ignored; and (2) increasing temperature is helpful to TP releasing from sediments. 相似文献
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The activities of particulate and soluble phosphatase were analyzed monthly for 1 year in the coastal ecosystems of the NW Mediterranean Sea. The mean contribution of the particulate activity increased from 56% at an MUF-P concentration of 30 μM to 77% at 0.04 μM. This particulate activity was negatively correlated with the DIP, DOP and TDP concentrations when the activities were related to the seawater volume, chlorophyll a or the protein concentration. The TDP correlations were highly significant (p: 0.001). The DOP correlations were significant (p: 0.04) and became highly significant (p: 0.009) at low DIP concentrations (<0.13 μM). The DIP correlations were significant (p: 0.04) only at low DOP concentrations (<0.18 μM). Thus, the effects of seawater DIP and DOP were found to be linked. The soluble activity exhibited distinct phosphatase fractions with high (0.5–29.5 μM) and low (0.02–2 μM) Km values, but none exhibited significant correlations with phosphorus compounds. 相似文献
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本研究在太湖梅梁湾采集沉积柱,采用一种自制的毫米级柱状沉积物自动垂向分层切割装置对表层50 mm沉积物进行垂向切割(间隔2 mm),结合高通量测序技术分析沉积物中细菌群落的毫米级垂向分布;同时采用毫米级高分辨透析技术和薄膜扩散梯度技术(DGT)分析溶解态和DGT可获取态铵态氮(NH4+-N)、硝态氮(NO3--N)、Fe、P的垂向分布特征。结果显示,沉积物中细菌群落与溶解态和DGT可获取态氮铁磷浓度在垂向上呈现显著的异质性。细菌硝酸盐还原主要发生在-16~0 mm沉积物深度,这可能导致了溶解态和DGT可获取态NO3--N含量在该沉积物深度的明显减少。细菌铁还原主要分布在-32~-18 mm沉积物深度,细菌硫酸盐还原主要分布在-50~-34 mm的沉积物深度;细菌硫酸盐还原是导致沉积物溶解态和DGT可获取态铁磷浓度从-32 mm随沉积物的深度增加而显著增加的主要原因。本研究加深了对富营养化湖泊沉积物中细菌影响氮磷在垂向上迁移转化的认识。 相似文献
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Stark JS Johnstone GJ Palmer AS Snape I Larner BL Riddle MJ 《Marine pollution bulletin》2006,52(12):1595-1610
The water quality of a marine embayment (Brown Bay) was monitored during the remediation of an abandoned waste disposal site at Casey Station, East Antarctica, using a combination of biomonitoring and chemical methods. The Antarctic amphipod Paramoera walkeri, in field mesocosms suspended in the water column, was deployed adjacent to the site and at two reference sites for periods of 14 days, repeated three times during the remediation period (December to February). Diffusive gradients in thin film (DGT) samplers were deployed for the same periods to provide estimates of dissolved metals. No difference in mortality of amphipods was observed between Brown Bay and reference sites. There were significant differences, however, in accumulated metal concentrations between amphipods from Brown Bay and reference sites, with greater concentrations of antimony, copper, cadmium, lead, iron and tin at Brown Bay. The melt water/runoff treatment strategy employed for the remediation was successful in preventing acute toxic effects, but water quality was reduced at Brown Bay, where increased metal bioavailability may have been high enough to induce chronic effects in some biota. DGT samplers were less sensitive than amphipods in detecting differences in metal concentrations between sites, indicating that metals bound to suspended particulates were a potentially significant source of contamination. 相似文献
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Maja A. Lazzaretti Kurt W. Hanselmann Helmut Brandl Daniel Span Reinhard Bachofen 《Aquatic Sciences - Research Across Boundaries》1992,54(3-4):285-299
P, Fe, Mn, and S species were analyzed in water samples from the sediment-water interface collected at four seasonally different times during the course of a year at two sampling sites in the southern basin of Lake Lugano (Lago di Lugano). The results reveal the strong influence of the biogeochemical processes in the sediment on the chemical composition of the lake water above. Consumption of oxygen and nitrate under oxic to microoxic conditions in the water column as well as sequential release of reduced manganese and iron under anoxic conditions was observed as a direct or indirect consequence of microbially mediated degradation of organic matter. The seasonal pattern observed for the release and the retainment of dissolved reduced iron and manganese correlates well with the one for dissolved phosphate. Iron, manganese and phosphorus cycling are coupled tightly in these sediments. Both sediment types act as sinks for hydrogen sulfide and sulfate. An inner-sedimentary sulfur cycle is proposed to couple iron, manganese and phosphorus cycling with the degradation of organic matter. Nutrient cycling at the sediment-water interface might thus be driven by a microbially regulated electron pumping mechanism. The results contribute to a better understanding of the role of sediment processes in the lake's internal phosphorus cycle and its seasonal dynamics. 相似文献