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1.
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   

2.
Study of interactions between surface-water and pore-water in lakes is complicated due to spatio-temporal heterogeneities in flow condition across the sediment–water interface. In this study, seasonal hypersaline Maharlu Lake was investigated by collecting surface-water and pore-water samples from four nests of multilevel piezometers installed at different distances from the inflow of rivers to the lake. The hydraulic heads in the piezometers as well as vertical profiles of Mg+2, Na/Cl, and Br/Cl were used to investigate both hydraulic and geochemical interactions between surface-water and pore-water in the lake. Depletion of lake surface water and pore water with respect to B, Br, Li+, K+, Mg2+ and the absence of Mg-K chlorides and sulphates in the lake bed sediments is probably due to leakage of highly evaporated residual brine from the lake. Hydraulic gradients in the multilevel piezometric nests indicate that a general downward flow from surface-water to pore-water occurs across sediment–water interface. Vertical profiles of Br/Cl, Mg2+, and Na/Cl showed that the maximum flow rate was more than 1 m/yr close to the mouth of the inflowing rivers. The downward vertical flow was limited in the area far from the inflowing rivers due to the presence of an impermeable confining halite layer which interrupts the hydraulic connection between shallow pore water (less than 50 cm deep) and deeper zones. The hydraulic and geochemical interactions between surface-water and pore-water across sediment–water interface in the Maharlu Lake are of interest to find out the fate of pollutants and their distribution in the lake.  相似文献   

3.
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   

4.
The effects of temperature, diffusive boundary-layer thickness, and sediment composition on fluxes of inorganic N and P were estimated for sediment cores with oxidized surfaces from nearshore waters (2?C10?m) of a montane oligotrophic lake. Fluxes of N and P were not affected by diffusive boundary-layer thickness but were strongly affected by temperature. Below 16?°C, sediments sequestered small amounts of P and released small amounts of N. Above 16?°C, the seasonal maximum water temperature, sediments were substantial sources of N (NH4 +?CN?=?2?C24?mg?m?2 d?1; NO3 ??+?NO2 ??CN?=?2?C5?mg?m?2 d?1) and P (0.1?C0.4?mg?m?2 d?1), indicating potential responsiveness of sediment?Cwater nutrient exchange, and of corresponding phytoplankton growth, to synoptic warming.  相似文献   

5.
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6.
《Marine pollution bulletin》2011,62(7-12):399-412
In order to quantify the spatial and seasonal variations of sediment oxygen consumption and nutrient fluxes, we performed a spatial survey in the south west lagoon of New Caledonia during the two major seasons (dry and wet) based on a network of 11 sampling stations. Stations were selected along two barrier reef to land transects representing most types of sediments encountered in the lagoon. Fluxes were measured using ex-situ sediment incubations and compared to sediment characteristics. Sediment oxygen consumption (SOC) varied between 500 and 2000 μmol m−2 h−1, depending on season and stations. Nutrient effluxes from sediment were highly variable with highest fluxes measured in muddy sediments near the coast. Inter-sample variability was as high as seasonal differences so that no seasonally driven temperature effect could be observed on benthic nutrient fluxes in our temperature range. Nutrient fluxes, generally directed from the sediment to the water column, varied between −5.0 and 70.0 μmol m−2 h−1 for ammonia and between −2.5 and +12.5 μmol m−2 h−1 for PO4 and NO2+3. SOC and nutrient fluxes were compared to pelagic primary production rates in order to highlight the tight coupling existing between the benthic and pelagic compartments in this shallow tropical lagoon. Under specific occasions of low pelagic productivity, oxygen sediment consumption and related carbon and nutrient fluxes could balance nearly all net primary production in the lagoon. These biogeochemical estimates point to the functional importance of sediment biogeochemistry in the lagoon of New Caledonia.  相似文献   

7.
Exchange of groundwater and lake water with typically quite different chemical composition is an important driver for biogeochemical processes at the groundwater‐lake interface, which can affect the water quality of lakes. This is of particular relevance in mine lakes where anoxic and slightly acidic groundwater mixes with oxic and acidic lake water (pH < 3). To identify links between groundwater‐lake exchange rates and acid neutralization processes in the sediments, exchange rates were quantified and related to pore‐water pH, sulfate and iron concentrations as well as sulfate reduction rates within the sediment. Seepage rates measured with seepage meters (?2.5 to 5.8 L m‐2 d‐1) were in reasonable agreement with rates inverted from modeled chloride profiles (?1.8 to 8.1 L m‐2 d‐1). Large‐scale exchange patterns were defined by the (hydro)geologic setting but superimposed by smaller scale variations caused by variability in sediment texture. Sites characterized by groundwater upwelling (flow into the lake) and sites where flow alternated between upwelling and downwelling were identified. Observed chloride profiles at the alternating sites reflected the transient flow regime. Seepage direction, as well as seepage rate, were found to influence pH, sulfate and iron profiles and the associated sulfate reduction rates. Under alternating conditions proton‐consuming processes, for example, sulfate reduction, were slowed. In the uppermost layer of the sediment (max. 5 cm), sulfate reduction rates were significantly higher at upwelling (>330 nmol g‐1 d‐1) compared to alternating sites (<220 nmol g‐1 d‐1). Although differences in sulfate reduction rates could not be explained solely by different flux rates, they were clearly related to the prevailing groundwater‐lake exchange patterns and the associated pH conditions. Our findings strongly suggest that groundwater‐lake exchange has significant effects on the biogeochemical processes that are coupled to sulfate reduction such as acidity retention and precipitation of iron sulfides. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

8.
High‐salinity paleowater from low‐permeability aquitards in coastal areas can be a major threat to groundwater resources; however, such water has rarely been studied. The chemical and isotopic compositions of porewater extracted from a 200‐m‐thick Quaternary sedimentary sequence in the western coastal plain of Bohai Bay, China, were analyzed to investigate the salinity origin and chemical evolution of porewater in aquitards. Porewater samples derived at depths shallower than 32 m are characterized by Cl‐Na type saline water (total dissolved solids [TDS], 10.9–84.3 g/L), whereas those at depths greater than 32 m comprise Cl·SO4‐Na type brackish water (TDS, 2.2–6.3 g/L). Saline porewater is interpreted as evaporated seawater prior to halite saturation, as evidenced by Cl‐Br relationships. Although substantial dilution of saline porewater with meteoric water is supported by a wider Cl? range and δ2H‐δ18O covariance, the original marine waters were not completely flushed out. The deeper brackish porewater is determined to be a mixture of fresher porewater and brine groundwater and had a component of old brine of less than 10%, as indicated by a mixing model defined using δ2H and Cl? tracers. Porewater δ2H‐δ18O relationships and negative deuterium excess ranging from ?25.9‰ to ?2.9‰ indicate the existence of an arid climate since Late Pleistocene in Tianjin Plain. The aquitard porewaters were chemically modified through water‐rock interactions due to the long residence time.  相似文献   

9.
Williams Lake, Minnesota is a closed‐basin lake that is a flow‐through system with respect to ground water. Ground‐water input represents half of the annual water input and most of the chemical input to the lake. Chemical budgets indicate that the lake is a sink for calcium, yet surficial sediments contain little calcium carbonate. Sediment pore‐water samplers (peepers) were used to characterize solute fluxes at the lake‐water–ground‐water interface in the littoral zone and resolve the apparent disparity between the chemical budget and sediment data. Pore‐water depth profiles of the stable isotopes δ18O and δ2H were non‐linear where ground water seeped into the lake, with a sharp transition from lake‐water values to ground‐water values in the top 10 cm of sediment. These data indicate that advective inflow to the lake is the primary mechanism for solute flux from ground water. Linear interstitial velocities determined from δ2H profiles (316 to 528 cm/yr) were consistent with velocities determined independently from water budget data and sediment porosity (366 cm/yr). Stable isotope profiles were generally linear where water flowed out of the lake into ground water. However, calcium profiles were not linear in the same area and varied in response to input of calcium carbonate from the littoral zone and subsequent dissolution. The comparison of pore‐water calcium profiles to pore‐water stable isotope profiles indicate calcium is not conservative. Based on the previous understanding that 40–50 % of the calcium in Williams Lake is retained, the pore‐water profiles indicate aquatic plants in the littoral zone are recycling the retained portion of calcium. The difference between the pore‐water depth profiles of calcium and δ18O and δ2H demonstrate the importance of using stable isotopes to evaluate flow direction and source through the lake‐water–ground‐water interface and evaluate mechanisms controlling the chemical balance of lakes. Published in 2003 by John Wiley & Sons, Ltd.  相似文献   

10.
湖泊底泥疏浚环境效应:Ⅰ.内源磷释放控制作用   总被引：9，自引：1，他引：8  
通过为期一年的疏浚模拟试验,在试验室培养疏浚与对照柱样研究了底泥疏浚对内源磷释放的控制效果．结果发现,疏浚表层30cm能够有效的消减沉积物中不f司形态磷含量与孔隙水中PO4^3-P含量．在一年的试验周期内,疏浚和对照柱沉积物-水界面的PO4^3-P通量分别为-143．8至14．4与-237．3至3047．6μg／（m^2&#183;d）,疏浚柱沉积物-水界面的磷通量总体上低于未疏浚对照的磷通量,尤其是在温度较高的月份,从2006年3-10月疏浚柱沉积物-水界面磷释放通量显著低于未疏浚对照柱,疏浚沉积物的磷的释放潜力低于未疏浚对照沉积物．研究结果表明,在外源磷得到有效控制的前提下,底泥疏浚是消减研究区内源磷负荷有效的技术手段．  相似文献   

11.
The hyporheic zone of riverbed sediments has the potential to attenuate nitrate from upwelling, polluted groundwater. However, the coarse‐scale (5–10 cm) measurement of nitrogen biogeochemistry in the hyporheic zone can often mask fine‐scale (<1 cm) biogeochemical patterns, especially in near‐surface sediments, leading to incomplete or inaccurate representation of the capacity of the hyporheic zone to transform upwelling NO3?. In this study, we utilised diffusive equilibrium in thin‐films samplers to capture high resolution (cm‐scale) vertical concentration profiles of NO3?, SO42?, Fe and Mn in the upper 15 cm of armoured and permeable riverbed sediments. The goal was to test whether nitrate attenuation was occurring in a sub‐reach characterised by strong vertical (upwelling) water fluxes. The vertical concentration profiles obtained from diffusive equilibrium in thin‐films samplers indicate considerable cm‐scale variability in NO3? (4.4 ± 2.9 mg N/L), SO42? (9.9 ± 3.1 mg/l) and dissolved Fe (1.6 ± 2.1 mg/l) and Mn (0.2 ± 0.2 mg/l). However, the overall trend suggests the absence of substantial net chemical transformations and surface‐subsurface water mixing in the shallow sediments of our sub‐reach under baseflow conditions. The significance of this is that upwelling NO3?‐rich groundwater does not appear to be attenuated in the riverbed sediments at <15 cm depth as might occur where hyporheic exchange flows deliver organic matter to the sediments for metabolic processes. It would appear that the chemical patterns observed in the shallow sediments of our sub‐reach are not controlled exclusively by redox processes and/or hyporheic exchange flows. Deeper‐seated groundwater fluxes and hydro‐stratigraphy may be additional important drivers of chemical patterns in the shallow sediments of our study sub‐reach. © 2015 The Authors. Hydrological Processes Published by John Wiley & Sons Ltd.  相似文献   

12.
滇池流域点源污染控制与存在问题解析   总被引：1，自引：0，他引：1  
采用间隙水连续采集法考察滇池和抚仙湖沉积物-水界面营养盐通量,并比较在氧气缺乏及氧气充足条件下界面的氮磷行为.结果表明,滇池草海沉积物-水界面营养盐通量显著高于滇池湖心及抚仙湖.对云南滇池及抚仙湖沉积物进行好氧和厌氧处理对照比较,结果显示,好氧组上覆水pH显著大于厌氧组,而间隙水pH在两处理组之间差异不显著;这可能与厌氧呼吸途径过程中产生酸性物质有关;而在两种处理条件下,间隙水均处于厌氧状态.较好氧条件而言,厌氧条件下间隙水磷和铵氮浓度的增加,与有机质矿化增强有关;而间隙水磷还可能受FeOOH-P模型控制.由分子扩散模型计算获得的界面磷或者铵氮扩散通量均高于表观通量,而且好氧条件下的扩散通量与表观通量之间的差异较厌氧条件下的大;这表明两种营养盐均存在释放潜力,但这种潜力的发挥受氧气的影响,较好氧条件而言,厌氧条件下使用分子扩散模型得到的界面营养盐扩散通量更接近于表观通量.  相似文献   

13.
The transport of water through the sediments of Lake Kinneret was estimated using tritium of fallout origin as a tracer. The calculation model takes into account the diffusion of the tracer and its decay, and allows for the advective flux through the sediment pores as a free parameter. The dependence of the interstitial diffusion constant on the porosity was assumed identical to that for chloride ions. Tritium profiles in nine cores were used for estimating the advective fluxes and velocities, by finding the best fit between data and model. Water advective fluxes of 3.4 g cm?2 yr?1 into the lake were found. This water flux is negligible in the hydrological balance of Lake Kinneret; but it carries along 7% of the unaccounted-for chloride input to the lake.  相似文献   

14.
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15.
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   

16.
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       下载免费PDF全文
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   

17.
Rare earth elements in the pore waters of reducing nearshore sediments   总被引：4，自引：0，他引：4  
The REE are mobile during early diagenesis in reducing nearshore sediments of Buzzards Bay leading to greatly enhanced concentrations in pore waters, e.g. 815 pmol kg−1 Nd and 1910 pmol kg−1 Ce within 30 cm of the sediment-seawater interface, about 10–50 times local seawater values. Two principal diagenetic reactions have been identified. Preferential Ce enrichment (positive Ce anomalies) and preferential heavy REE enrichment (light REE removal) in the pore waters is associated with redox cycling of Fe and Mn within the upper few centimeters of the sediment. Release of REE, without fractionation, from sediments and addition to pore waters occurs deeper within the sediment column. The impact on the bulk sediment chemistry is undetectable but the porewater gradients imply that there are significant dissolved REE fluxes, both internal to the sediment system and across the sediment-seawater interface.  相似文献   

18.
云南阳宗海大气氮、磷沉降特征   总被引：1，自引：0，他引：1       下载免费PDF全文
大气氮、磷沉降是湖泊水体氮、磷入湖的重要途径之一.为了解阳宗海氮、磷沉降对湖泊富营养化的潜在影响,于2012年5月-2014年4月通过监测阳宗海大气氮、磷沉降,估算氮、磷的大气沉降通量,揭示阳宗海大气氮、磷沉降随时间变化的特征,分析其来源、影响因素等.由于阳宗海是磷限制湖泊,本研究在估算大气氮、磷沉降通量的基础上,特别比较了大气磷沉降入湖量与非点源磷的入湖量,以此评估大气沉降输入磷对湖泊富营养化的潜在影响.研究结果表明:阳宗海总氮年平均沉降通量为248 mg/m~2,春、夏、秋和冬季平均分别为200、306、274和214 mg/m~2,其中夏季沉降通量最大,原因与降雨量增加有关;总磷年平均沉降通量为24 mg/m~2,春、夏、秋和冬季平均分别为18、31、19和27 mg/m~2.大气磷沉降与输入阳宗海的总磷量相比很小,对阳宗海富营养化影响较小.  相似文献   

19.
The purpose of this study was to examine the historical change in sedimentation rates in lakes that have been impacted by river regulation and agricultural activities in the Ishikari River floodplain. We dated sediment cores using caesium‐137 (137Cs) dating and tephrochronology, and we estimated sediment sources from 137Cs concentrations in the topsoil of representative land covers. We found that, between 1739 and 1963, the distance between the lake and the main river channel and whether or not the lake was connected to the river affected the sedimentation rates. After 1963, agricultural drainage systems were established in the Ishikari River floodplain. The average sedimentation rate before and after the construction of drainage ditches varied between 1–66 and 87–301 mg cm–2 a–1, respectively. The increase in the sedimentation rate after 1963 was caused by the construction of a number of drainage networks, as well as extensive cultivation activity and/or fragmentation of the swamp buffers surrounding the lakes. The 137Cs activities at the surfaces of the lake as well as the catchment‐derived 137Cs contributions and 137Cs inventory in the lake profiles were used to examine the sediment influx from the various drainage areas after the establishment of the drainage system. Our results indicate that the majority of the lake sediments were derived from cultivated areas, and therefore the catchment‐derived 137Cs contribution in the lakes was strongly correlated with the sedimentation rate. The 137Cs inventory across all of the lake profiles was also significantly greater than the atmospheric fallout. We identified a negative correlation between the 137Cs lake profile inventory and the sedimentation rate. This is because the sediment originating from the drainage areas contained low 137Cs concentrations, which diluted the overall concentration of 137Cs in the lake sediment. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   

20.
白洋淀沉积物氮磷赋存特征及其内源负荷   总被引：11，自引：2，他引：9  
杜奕衡  刘成  陈开宁  古小治  黄蔚  韦众 《湖泊科学》2018,30(6):1537-1551
白洋淀环境整治对区域生态文明建设具有重要意义，然而，目前对加剧白洋淀富营养化的内源氮、磷污染负荷依然缺乏系统的研究.本研究以野外调研和室内培养实验相结合形式，在白洋淀主要水域内采集原位柱状沉积物样品，详细地研究了白洋淀沉积物中氮、磷赋存形态、间隙水中氮、磷剖面特征以及沉积物-水界面氮、磷交换特征.结果表明，白洋淀沉积物总氮、总磷含量分别为1230.8~9559.0 mg/kg（均值2379.5 mg/kg）和344.4~915.4 mg/kg（均值608.4 mg/kg），氮、磷累积污染量大.沉积物中铵态氮赋存量大（3.2~175.8 mg/kg），由此导致间隙水中铵态氮浓度较高，最高达到28.8 mg/L.沉积物磷形态以Ca-P和Fe-P为主，分别占总量的38.3%~76.1%和3.98%~18.0%，间隙水中磷酸盐浓度已接近甚至高于国内外典型富营养湖区.间隙水中高浓度的铵态氮和磷酸盐导致沉积物-水界面氮、磷交换通量较高，铵态氮平均释放和扩散通量分别为106.37和12.42 mg/（m2·d）；磷酸盐平均释放和扩散通量分别为15.06和2.33 mg/（m2·d），沉积物内源氮、磷污染负荷较高，已严重威胁到白洋淀水环境质量，迫切需要整治.其中，北部河口区域以及中部府河入湖区和人口密集活动区沉积物氮、磷内源负荷尤为突出，应成为白洋淀沉积物内源污染整治的关键区域.  相似文献   

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