The freshwater dissolved organic matter fluorescence–total organic carbon relationship

The fluorescent properties of dissolved organic matter (DOM) enable comparisons of humic‐like (H‐L) and fulvic‐like (F‐L) fluorescence intensities with dissolved organic carbon (DOC) in aquatic systems. The fluorescence‐DOC relationship differed in gradient, i.e. the fluorescence per gram of carbon, and in the strength of the correlation coefficient. We compare the fluorescence intensity of the F‐L and H‐L fractions and DOC of freshwater DOM in north Shropshire, England, featuring a river, wetland, spring, pond and sewage DOM sources. Correlations between fluorescence and DOC varied between sample sites. Wetland water samples for the F‐L peak gave the best correlation, r = 0·756; the lowest correlation was from final treated sewage effluent, r = 0·167. The relationship between fluorescence and DOC of commercially available International Humic Substances Society standards were also examined and they generally showed a lower fluorescence per gram of carbon for the F‐L peak than the natural samples, whereas peat wetland DOM gave a greater fluorescence per gram of carbon than river DOM. Here, we propose the strength of the fluorescence–DOC correlation to be a useful tool when discriminating sources of DOM in fresh water. Copyright © 2007 John Wiley & Sons, Ltd.     

Spectrophotometric discrimination of river dissolved organic matter

There is a need to be able to differentiate the dissolved organic matter (DOM) fraction in river waters. Research in the 1970s and 1980s has attempted to utilize both absorbance and fluorescence to distinguish between DOM fractions in river waters, but both were limited by the available technology. Total organic carbon content has, therefore, been widely used as a standard method of measuring DOM concentration, although it has little power to differentiate DOM fractions. Recent advances in fluorescence spectrophotometry enable rapid and optically precise analysis of DOM. Here, we show how a combination of both fluorescence and absorbance can be used to discriminate statistically between spatial variations of DOM in tributaries in a small catchment of the Ouseburn, NE England. The results of the discriminant analysis suggest that about 70% of the samples can be correctly classified to its tributary. Discriminant function 1 explains 60·8% of the variance in the data and the fulvic‐like fluorescence intensity has the largest absolute correlation within this function; discriminant function 2 explains a further 21·5% of the variance and the fulvic‐like fluorescence emission wavelength has the largest absolute correlation within this function. The discriminant analysis does not correctly classify all tributaries every time, and successfully discriminates between the different tributaries 70% of the time. Occasions when the tributary waters are less well discriminated are due to either episodic pollution events (at two sites) or due to tributaries that have strong seasonal trends in spectrophotometric parameters, which allows the sites to be misclassified. Results suggest that spectrophotometric techniques have considerable potential in the discrimination of DOM in rivers. Copyright © 2002 John Wiley & Sons, Ltd.     

太湖梅梁湾有色可溶性有机物的空间分布及光学行为

2004年3月对太湖梅梁湾有色可溶性有机物(CDOM)的吸收和荧光等光学行为进行研究,并由此探讨了CDOM的空间分布．结果表明,溶解性有机碳(DOC)的浓度在10．48-19．72 mg／L间变化,其均值为13．20±2．79 mg／L;CDOM在280 nm,355 nm和440 nm的吸收系数分别为18．73-31．91 m-1(平均值23．19±4．36 m-1)、4．63-7．14 m-1(平均值5．76±0．91 m-1)、1．45-2．99 m-1(平均值1．92±0．40 m-1);355 nm波长处CDOM的比吸收系数为0．34-0．57 L／(mg·m),平均值0．44±0．06 L/(mg·m);表征CDOM分子大小的比值a(250)／a(365)变化范围为5．05-7．55;355 nm的激发波长、450 nm的发射波长处的荧光值的变化范围0．79-3 04 nm-1(平均值1．69±0．77 nm-1)．CDOM吸收系数、DOC浓度、荧光强度的分析显示CDOM浓度呈现从河口往湾内、湾口递减的趋势．CDOM吸收与DOC浓度的相关性随波长的降低而增加,在短波部分存在明显的正相关．355 nm处的荧光值、DOC浓度与CDOM吸收系分别存在如下显著性正相关关系:Fn(355)=0．692(±0．135)a(355)-2．297(±0．786),a(355)=0．233(±0．061)DOC 2．690(±0．816)．280 -500 nm、280-360 nm、360-440 nm指数函数斜率S值分别为13．86±0．91、18．54±1．11、12．93±0．92μm-1,S值与比吸收系数之间存在显著的负线性相关关系,而与a(25)／a(365)值则存在显著的正线性关系．比吸收系数越大,a(250)／a(365)值和S值就越小,对应的CDOM分子量就越大,腐质酸的比例就越高．     

江苏省西部湖泊溶解性有机物光谱学特征和来源解析

利用光谱学手段研究江苏省西部湖泊表层水体中溶解性有机物(DOM)组成与结构,并对其来源进行分析.单位浓度可溶性有机碳在254和280 nm波长下的吸光度值(SUVA)测定结果表明,各湖泊芳香性程度及分子量大小依次为邵伯湖>天岗湖>白马湖>石臼湖>洪泽湖>固城湖>骆马湖>高邮湖>宝应湖.特定波长下吸光度的比值(E2/E3、E3/E4)显示邵伯湖和白马湖中的DOM结构复杂、分子量大、苯环多,以腐殖酸为主要成分;其它湖泊的DOM腐殖化程度较低,以富里酸为主.指数函数曲线斜率(S275～295nm)拟合结果也同样表明邵伯湖DOM分子量最大,而宝应湖最低.各湖泊荧光指数和生物指数分别处于1.13～1.30和0.47～0.67范围内,体现出DOM强烈的陆源性.四个主要荧光峰的相对荧光强度之间均存在良好的相关性,表明这些湖泊的类腐殖酸及类蛋白物质可能有着相同的来源.结合这些湖泊的特征及流域经济发展水平,可以初步推断经入湖河流携带的由农业及其下游产业产生的有机质是江苏西部湖泊中DOM的主要来源.     

太湖冬季有色可溶性有机物吸收荧光特性及遥感算法

基于2006年和2007年1月两次太湖采样,对50个点位的有色可溶性有机物(CDOM)光谱吸收、荧光、溶解性有机碳(DOE)浓度及遥感反射率进行测定与分析,探讨冬季太湖CDOM的吸收荧光特性及空间分布,建立CDOM吸收系数的遥感反演算法.结果表明,太湖冬季CDOM在355nm处吸收系数a(355)变化范围和均值分别为1...     

典型湖泊天然有机质与四环素的相互作用

采用荧光滴定法研究四环素(tetracycline,TC)与太湖溶解性有机质(dissolved organic matter,DOM)和玄武湖DOM的相互作用.三维荧光光谱结合平行因子分析显示,2个湖泊的DOM含有3个荧光组分:类富里酸组分C1、类色氨酸组分C2和类络氨酸组分C3.其中C2的荧光强度远高于C1和C3,是DOM的主要荧光组成.3个荧光组分与TC发生了不同程度的静态猝灭,特别当TC浓度为45.5μmol/L时,类蛋白组分的荧光强度完全被猝灭(100%),并且猝灭作用改变了DOM分子的微环境极性.同步荧光光谱联合二维相关图谱进一步表明类色氨酸组分优先和TC发生猝灭作用,其次为类络氨酸组分和类富里酸组分.Ryan-Weber方程适于拟合DOM与TC的猝灭过程,2个湖泊的DOM中3个荧光组分的络合常数lg K值范围为5.05~5.85,大小顺序为C2C3C1.因此,类蛋白组分为主的DOM对TC的络合作用大于类腐殖组分为主的DOM,影响抗生素在湖泊水体中的生物有效性和生态毒性.     

Continuous fluorescence assessment of organic matter variability on the Bournbrook River,Birmingham, UK

Continuous monitoring of dissolved organic matter (DOM) character and concentration at hourly resolution is rare, despite the importance of analysing organic matter variability at high‐temporal resolution to evaluate river carbon budgeting, river water health by detecting episodic pollution and to determine short‐term variations in chemical and ecological function. The authors report a 2‐week experiment performed on DOM sampled from Bournbrook, Birmingham, UK, an urban river for which spectrophotometric (fluorescence, absorbance), physiochemical (dissolved organic carbon [DOC], electrical conductivity, pH) and isotopic (D/H) parameters have been measured at hourly frequency. Our results show that the river had sub‐daily variations in both organic matter concentration and characteristics. In particular, after relatively high‐magnitude precipitation events, organic carbon concentration increased, with an associated increase in intensity of both humic‐like and tryptophan‐like fluorescence. D/H isotopic ratio demonstrates different hydrological responses to different rainfall events, and organic matter character reflects this difference. Events with precipitation < 2 mm typically yielded isotopically heavy water with relatively hydrophilic DOM and relatively low specific absorbance. Events with precipitation > 2 mm had isotopically lighter water with higher specific absorbance and a decrease in the proportion of microbially derived to humic‐like fluorescence. In our heavily urbanized catchment, we interpret these signals as one where riverine DOM is dominated by storm sewer‐derived ‘old’ organic matter at low‐rainfall amounts and a mixed signal at high‐precipitation amounts where ‘event’ surface runoff‐derived organic matter dominate during storm sewer and combined sewer overflow routed DOM. Copyright © 2009 John Wiley & Sons, Ltd.     

云南高原湖泊有色可溶性有机物和颗粒物光谱吸收特性

云南高原湖泊是我国湖泊分布最密集的五大湖群之一,不但湖泊数量众多而且类型多样.由于湖泊所处位置海拔较高,容易受只益增强UV-B辐射影响.通过对云南高原34个湖泊有色可溶性有机物和颗粒物吸收测定,分析其光谱吸收特性及对总吸收的贡献,有利于深刻理解紫外辐射在高原湖泊内衰减.不同湖泊间CDOM吸收差异明显,其大小与水体营养盐状况相关,CDOM吸收系数与水体总氮存在显著正相关.增加背景项的指数函数模型能最好模拟CDOM光谱吸收.除在浮游植物浓度非常高的杞麓湖、听湖、星云湖,颗粒物吸收系数在675nm附近存在一个吸收蜂外,其它湖泊总颗粒物光谱吸收大致随波长的增加吸收系数逐渐降低,呈现非色素颗粒物光谱吸收特征,整体上颗粒物吸收以非色素颗粒物为主.CDOM对总吸收的贡献主要集中在600nm以下波长,尤其是400nm以下的紫外波段,其在紫外波段(350-400nm)的贡献明显要大于光合有效辐射波段(400-700nm)(ANOVA,P<0.001).特别对于透明度SD≥1.0的清澈型湖泊,CDOM吸收对紫外辐射衰减的贡献更大,其吸收很大程度上决定了紫外辐射的影响深度.     

淀山湖有色可溶性有机物的光谱吸收特性

探讨了淀山湖水体中有色可溶性有机物(CDOM)的光谱吸收特性,CDOM与叶绿素a、浊度和COD等水质参数的关系,以及不同波段范围内CDOM光谱吸收形状(指数函数斜率S值)的变化.结果表明:淀山湖CDOM吸收系数不高,在355 nm波长处的吸收系数变化范围是6.95-10.28 m-1,而且湖南区高于湖北区;CDOM吸收系数和叶绿素a、浊度、COD等水质参数的相关性都不高,证明湖中的CDOM主要来自于城镇生活污水和工业废水的排放;CDOM吸收系数在300-500 nm范围内随着波长的增加呈指数递减,超过500 nm之后呈线性递减,在300-500 nm波段范围内指数函数的曲线斜率S为11.7-14.8 μm-1,在501-750 nm波段范围内波长每增1 nm,CDOM的吸收系数减小0.0021 m-1.     

鄱阳湖水体溶解有机质分子量分布、荧光特征及对重金属分布的影响

溶解有机质(DOM)在环境水体中广泛存在,具有连续的分子量分布特征,并可显著影响水体中污染物的迁移转化和归趋行为.于2019年春季采集鄱阳湖全湖水样,采用超过滤技术将DOM样品分为低分子量(LMW,<1 kDa)和高分子量(HMW,1 kDa～0.45μm)组分,通过三维荧光光谱结合平行因子分析(EEM-PARAFAC)和ICP-MS分析不同分子量区间有机组分和重金属含量.结果表明,鄱阳湖水体DOM中LMW-DOM占比为43%～55%,HMW-DOM占比为45%～57%.平行因子模型提取出3个相互独立的荧光组分,分别为类富里酸组分C1、C2和类腐殖酸组分C3. 60%～73%的C1分布在LMW中,77%～93%的C2分布在HMW中,而C3几乎平均分布在LMW-和HMW-DOM中,可能与C1、C2、C3组分分别含有的传统荧光峰有关.通过对荧光参数FIX(<1.4)、BIX(<0.8)的计算发现鄱阳湖DOM陆源特征显著,且HMW组分具有比LMW组分更高的陆源特征和芳香度.重金属检测结果表明Cr、Mn、Fe、Pb则主要分布在HMW中(63%～94%),As、Cd、Ba、Se...     

抚仙湖有色可溶性有机物的来源组成与时空变化

基于2017年1-12月在抚仙湖开展的逐月观测,利用紫外-可见吸收光谱和三维荧光光谱技术探讨该湖有色可溶性有机物（CDOM）的来源组成及时空变化特征.12个月CDOM吸收值a（254）的均值为3.47±0.57 m^-1,范围为1.82~5.22 m^-1,说明CDOM丰度较低.平行因子分析结果给出了2种类酪氨酸荧光组分（C1和C3）、1种类色氨酸荧光组分（C2）、1种类腐殖质荧光组分（C4）,12个月内源组分（C1+C3）对总荧光强度的平均贡献为65.81%±15.38%,外源组分（C2+C4）的平均贡献为34.19%±15.38%;荧光指数FI的均值为1.73±0.14,腐殖化指数HIX的均值为1.02±0.37,生源化指数BIX的均值为1.23±0.27,说明CDOM主要为微生物内源产生.时空变化方面,春（3-5月）、夏（6-8月）、秋（9-11月）和冬（1、2、12月）季的a（254）分别为3.20±0.47、3.76±0.64、3.67±0.50和3.23±0.38 m^-1,夏季和秋季均显著高于冬季和春季;CDOM丰度及内外源组分的空间分布具有季节异质性,可能与流域土地利用、河流输入、降雨、温度、光辐射等因素有关.     

Diurnal variability in riverine dissolved organic matter composition determined by in situ optical measurement in the San Joaquin River (California,USA)

Dissolved organic matter (DOM) concentration and composition in riverine and stream systems are known to vary with hydrological and productivity cycles over the annual and interannual time scales. Rivers are commonly perceived as homogeneous with respect to DOM concentration and composition, particularly under steady flow conditions over short time periods. However, few studies have evaluated the impact of short term variability (<1 day) on DOM dynamics. This study examined whether diurnal processes measurably altered DOM concentration and composition in the hypereutrophic San Joaquin River (California) during a relatively quiescent period. We evaluated the efficacy of using optical in situ measurements to reveal changes in DOM which may not be evident from bulk dissolved organic carbon (DOC) measurement alone. The in situ optical measurements described in this study clearly showed for the first time diurnal variations in DOM measurements, which have previously been related to both composition and concentration, even though diurnal changes were not well reflected in bulk DOC concentrations. An apparent asynchronous trend of DOM absorbance and chlorophyll‐a in comparison to chromophoric dissolved organic matter (CDOM) fluorescence and spectral slope S_290–350 suggests that no one specific CDOM spectrophotometric measurement explains absolutely DOM diurnal variation in this system; the measurement of multiple optical parameters is therefore recommended. The observed diurnal changes in DOM composition, measured by in situ optical instrumentation likely reflect both photochemical and biologically‐mediated processes. The results of this study highlight that short‐term variability in DOM composition may complicate trends for studies aiming to distinguish different DOM sources in riverine systems and emphasizes the importance of sampling specific study sites to be compared at the same time of day. The utilization of in situ optical technology allows short‐term variability in DOM dynamics to be monitored and serves to increase our understanding of its processing and fundamental role in the aquatic environment. Copyright © 2007 John Wiley & Sons, Ltd.     

太湖入湖河口和开敞区CDOM吸收和三维荧光特征

应用吸收和三维荧光光谱对2007年夏季太湖入湖河口和大太湖开敞区有色可溶性有机物(CDOM)浓度及来源进行研究.结果表明,河口区和开敞区CDOM吸收系数a(355)存在显著空间差异,河口区明显大于开敞(ANOVA,P<0.001),a(355)最大值出现在大浦河口和竺山湾漕桥河几附近,最小值出现在东太湖和胥口湾.a(355)与溶解性有机碳、化学耗氧量浓度存在显著正相关.所有样品一般都含有4个明显的荧光峰,包括1个可见光区的类腐殖质荧光C峰,1个紫外光区的类腐殖酸荧光A峰,2个类蛋白荧光B峰和D峰.河口区外源输入的类腐殖质荧光非常强,最著大于开敞区(ANOVA,P<0.05).而河口区和开敞区类蛋白荧光没有显著性差异,反映开敞区除外源河流输入外,内源生物降解等对类蛋白荧光贡献增加.在河口区B、C峰的比值r(B/C)/b于1,均值为0.62±0.14、在开敞区r(B/C)除12#是0.92,其他值均大于1,均值为1.12±0.13,初步判断r(B/C)可以作为区分CDOM来源的重要参数.CDOM吸收a(355)与类腐殖质荧光C峰、A峰均存在极显著的正相关,而与类蛋白荧光相关性则明显下降,与D峰存在显著正相关,与B峰没有显著相关.     

峡谷分层型水源水库表层沉积物溶解性有机物光谱特征

结合三维荧光光谱技术（EEMs）与紫外吸收光谱（UV-vis）,并利用平行因子分析（PARAFAC）的方法,对金盆水库表层沉积物中溶解性有机质（DOM）光谱的空间分布特征及来源进行分析,并探讨沉积物DOM的荧光组分与可溶性有机氮（SON）、可溶性无机氮（SIN）之间的相关性.结果表明,金盆水库表层沉积物DOM由3类荧光组分组成,分别是类富里酸C1（235 nm,315 nm/430 nm）、类色氨酸C2（220 nm,275 nm/330 nm）和类胡敏酸C3（265 nm/520 nm）,各组分荧光强度占总荧光强度百分比的平均值分别为43.15%、31.54%和25.31%.表层沉积物DOM浓度在空间上呈现从上游到主库区先减少后增加的趋势.光谱斜率S_275-295、S_350-400和光谱斜率比S_R反映出各采样点陆源与内源占比的差异性.荧光指数、自生源指标和腐殖化指标都表明金盆水库沉积物DOM的来源具有内源与陆源双重特征.相关性分析表明,表层沉积物DOM各组分与SON和SIN均呈显著正相关,说明DOM与氮元素的迁移转化密切相关.     

高邮湖、南四湖和东平湖有色可溶性有机物来源组成特征

高邮湖、南四湖和东平湖作为南水北调东线枢纽湖泊,其水质状况对保障调水安全起到关键性作用本文运用三维荧光光谱平行因子分析法(EEMs-PARAFAC)分析了3个湖泊在不同水文情景下有色可溶性有机物(CDOM)吸收、荧光光谱特征以及荧光组分与主要水质参数的相关性,以探究3个湖泊CDOM来源组成特征结果表明,平行因子分析法解析CDOM三维荧光图谱,得到陆源类腐殖质C1、类色氨酸C2和类酪氨酸C3不同水文情景对高邮湖CDOM来源与结构组成影响较明显,丰水期其类腐殖质荧光强度显著大于枯水期(t-test,P<0.01),并且与a(254)呈正相关(R²=0.85,P<0.01),表明类腐殖质是CDOM主要部分,该荧光组分贡献率可达50%[F_maxC1/(F_maxC1+F_maxC2+F_maxC3)×100%],高邮湖受到入湖河流来水的影响较大,丰水期入湖口附近荧光强度明显高于其他水域东平湖和南四湖CDOM来源组成特征相似,丰水期东平湖和南四湖组分C2和C3显著低于枯水期(t-t...     

Dissolved organic matter dynamics during the spring snowmelt at a boreal river valley mire complex in Northwest Russia

Boreal mire landscapes are rich in soil carbon and significantly contribute to the carbon input of aquatic ecosystems. They are composed of different mesoscale ecohydrological subunits, whose individual contributions to the water and carbon export of mire catchments are not well understood. The spring snowmelt period is the major hydrological event in the annual water cycle of the boreal regions and strongly influences the carbon flux between the terrestrial and aquatic systems. The aim of this study was (1) to provide a conceptual understanding of the spatial and temporal dynamics of the surface water chemistry along a swamp forest‐fen‐bog gradient during the snowmelt period, (2) to quantify the exported dissolved organic carbon (DOC) content in the runoff and (3) to identify the ecohydrological landscape unit that contributes most to DOC export during the snowmelt period in a heterogeneous mire complex in Northwest Russia. The highest DOC concentrations were detected in the swamp forest, and the lowest concentrations were observed at the treeless bog by the end of the snowmelt period (swamp forest: 37–43 mg l^?1, bog: 13–17 mg l^?1). During the spring snowmelt period, a significant amount (~1.7 g C m^?2) of DOC was transferred by the ~74 mm of runoff from the catchment into the river. Variability in the thawing periods led to differences in the relative contributions of each ecohydrological zone to the carbon export measured at a stream channel draining the studied part of the mire complex. An increased understanding of the variation in DOC concentrations and contributions from the mesoscale ecohydrological subunits to carbon export can help to predict the potential regional loss of DOC based on land cover type under climate change. Copyright © 2015 John Wiley & Sons, Ltd.     

River network travel time is correlated with dissolved organic matter composition in rivers of the contiguous United States

Most terrestrial allochthonous organic matter enters river networks through headwater streams during high flow events. In headwaters, allochthonous inputs are substantial and variable, but become less important in streams and rivers with larger watersheds. As allochthonous dissolved organic matter (DOM) moves downstream, the proportion of less aromatic organic matter with autochthonous characteristics increases. How environmental factors converge to control this transformation of DOM at a continental scale is less certain. We hypothesized that the amount of time water has spent travelling through surface waters of inland systems (streams, rivers, lakes, and reservoirs) is correlated to DOM composition. To test this hypothesis, we used established river network scaling relationships to predict relative river network flow-weighted travel time (FWTT) of water for 60 stream and river sites across the contiguous United States (3090 discrete samples over 10 water years). We estimated lentic contribution to travel times with upstream in-network lake and reservoir volume. DOM composition was quantified using ultraviolet and visible absorption and fluorescence spectroscopy. A combination of FWTT and lake and reservoir volume was the best overall predictor of DOM composition among models that also incorporated discharge, specific discharge, watershed area, and upstream channel length. DOM spectral slope ratio (R² = 0.77) and Freshness Index (R² = 0.78) increased and specific ultraviolet absorbance at 254 nm (R² = 0.68) and Humification Index (R² = 0.44) decreased across sites as a function of FWTT and upstream lake volume. This indicates autochthonous-like DOM becomes continually more dominant in waters with greater FWTT. We assert that river FWTT can be used as a metric of the continuum of DOM composition from headwaters to rivers. The nature of the changes to DOM composition detected suggest this continuum is driven by a combination of photo-oxidation, biological processes, hydrologically varying terrestrial subsidies, and aged groundwater inputs.     

Distribution,characteristics and potential impacts of chromophoric dissolved organic matter (CDOM) in Hudson Strait and Hudson Bay,Canada

The characteristics of chromophoric dissolved organic matter (CDOM) were studied in Hudson Bay and Hudson Strait in the Canadian Arctic. Hudson Bay receives a disproportionately large influx of river runoff. With high dissolved organic matter (DOM) concentrations in Arctic rivers the influence of CDOM on coastal and ocean systems can be significant, yet the distribution, characteristics and potential consequences of CDOM in these waters remain unknown. We collected 470 discrete water samples in offshore, coastal, estuarine and river waters in the region during September and October 2005. Mixing of CDOM appeared conservative with salinity, although regional differences exist due to variable DOM composition in the rivers discharging to the Bay and the presence of sea-ice melt, which has low CDOM concentrations and low salinity. There were higher concentrations of CDOM in Hudson Bay, especially in coastal waters with salinities <28$<28$, due to river runoff. Using CDOM composition of water masses as a tracer for the freshwater components revealed that river runoff is largely constrained to nearshore waters in Hudson Bay, while sea-ice melt is distributed more evenly in the Bay. Strong inshore–offshore gradients in the bio-optical properties of the surface waters in the Hudson Bay cause large variation in penetration of ultraviolet radiation and the photic depth within the bay, potentially controlling the vertical distribution of biomass and occurrence of deep chlorophyll maxima which are prevalent only in the more transparent offshore waters of the bay. The CDOM distribution and associated photoprocesses may influence the thermodynamics and stratification of the coastal waters, through trapping of radiant heating within the top few meters of the water column. Photoproduction of biologically labile substrates from CDOM could potentially stimulate the growth of biomass in Hudson Bay coastal waters. Further studies are needed to investigate the importance of terrestrial DOM in the Hudson Bay region, and the impact of hydroelectric development and climate change on these processes.     

Hydroclimatic controls on dissolved organic matter (DOM) characteristics and implications for trace metal transport in Hwangryong River Watershed,Korea, during a summer monsoon period

Frequent heavy rainfalls during the East Asian summer monsoon drastically increase water flow and chemical loadings to surface waters. A solid understanding of hydroclimatic controls on watershed biogeochemical processes is crucial for water quality control during the monsoon period. We investigated spatio‐temporal variations in the concentrations and spectroscopic properties of dissolved organic matter (DOM) and the concentrations of trace metals in Hwangryong River, Korea, during a summer period from the relatively dry month of June through the following months with heavy rainfall. DOM and its spectroscopic properties differed spatially along the river, and also depended on storm and flow characteristics around each sampling time. At a headwater stream draining a forested watershed, the concentrations (measured as dissolved organic carbon (DOC)), aromaticity (measured as specific UV absorbance at 254 nm), and fulvic acid‐ and protein‐like fluorescence of DOM were higher in stormflow than in baseflow waters. DOC concentrations and fluorescence intensities increased along the downstream rural and urban sites, in which DOC and fluorescence were not higher in stormflow waters, except for the ‘first flush’ at the urban site. The response of DOM in reservoir waters to monsoon rainfalls differed from that of stream and river waters, as illustrated by storm‐induced increases in DOM aromaticity and fulvic‐like fluorescence, and no significant changes in protein‐like fluorescence. The results suggest that surface water DOM and its spectroscopic properties differentially respond to changes in hydroclimatic conditions, depending on watershed characteristics and the influence of anthropogenic organic matter loadings. DOC concentrations and intensities of spectroscopic parameters were positively correlated with some of the measured trace metals (As, Co, and Fe). Further research will be needed to obtain a better understanding of climate effects on the interaction between DOM and trace metals. Copyright © 2006 John Wiley & Sons, Ltd.     

铁（氢）氧化物介导的溶解性有机质、无机磷的固定及相互作用研究进展

铁(氢)氧化物介导的溶解性有机质(DOM)和无机磷(DIP)的固定在水生态系统中普遍存在,对碳、磷元素的生物地球化学循环有重要的影响.铁(氢)氧化物主要通过吸附和共沉淀两种过程固定DOM和DIP,且铁(氢)氧化物、DOM和DIP三者存在复杂的相互作用.本文主要从铁(氢)氧化物对DOM和DIP的固定,铁(氢)氧化物、DOM和DIP之间的相互影响等方面综述了相关研究进展,梳理了铁(氢)氧化物、DOM和DIP在吸附和共沉淀过程中的相互作用机制与影响因素.DOM的存在会通过占据铁(氢)氧化物表面吸附点位、络合、抑制铁水解沉淀等途径影响铁(氢)氧化物对DIP的固定;且不同机制与DOM的不同性质如分子大小、芳香组分、羧基官能团含量等有关.而DIP的存在会改变铁(氢)氧化物对DOM的固定分馏过程,改变溶液中DOM的组分和性质.在明晰三者相互作用基础上,探讨了铁(氢)氧化物介导的DOM和DIP的固定过程对湖泊内源磷释放和碳埋藏的可能影响,并对未来的研究方向进行了展望.