喀斯特筑坝河流中生物碳泵效应的碳施肥及对水化学时空变化的影响——以贵州平寨水库及红枫湖为例

耦联水生光合作用的碳酸盐风化碳汇是全球碳循环的重要组成部分,而生物碳泵效应是稳定碳酸盐风化碳汇的关键机制.河流筑坝后,生物碳泵效应的变化、控制因素及对水化学影响的研究甚少.本研究对2个喀斯特筑坝河流平寨水库和红枫湖进行系统采样,以研究河流筑坝后生物碳泵效应的变化、控制因素及对水化学的影响.研究结果表明,入库河流的水化学变化不明显,而2个水库的水化学则表现出显著的季节变化特征,具体表现为水库的水温和pH均呈现出夏季高、冬季低的变化特征,而电导率（EC）、HCO₃^-浓度和pCO₂则表现出夏季低、冬季高的季节变化特征.以叶绿素a（Chl.a）浓度和溶解氧（DO）饱和度指代的生物碳泵效应则是在夏季最强、冬季最弱.生物碳泵效应利用溶解性无机碳（DIC）,形成有机质并释放出氧气,是造成夏季水库pH值和DO饱和度升高,电导率（EC）、HCO₃^-浓度和pCO₂降低的主要因素.空间上,水库的Chl.a浓度及DO饱和度均大于河水,EC、HCO₃^-浓度和pCO₂均小于河水,这表明河流筑坝后,由于水库的“湖泊化”导致水库的生物碳泵效应显著提高.通过对Chl.a与碳、氮和磷浓度及化学计量比的相关性分析发现,平寨水库和红枫湖的生物碳泵效应受到碳施肥的影响.平寨水库和红枫湖水库生物碳泵效应碳施肥机制的发现,表明在喀斯特地区,生物碳泵效应不仅受到氮磷元素的控制,也受到碳元素的控制,因此在富营养化湖泊治理时,也应考虑碳的影响.     

生态补水对白洋淀流域地表水和地下水水化学特征的影响

生态补水是维持和改善白洋淀生态环境的重要途径.为研究生态补水对白洋淀水环境的影响,分别在补水前与补水后采集淀水、河水及地下水样品,分析区域地表水和地下水水化学特征.结果表明：（1）白洋淀补水前、后地表水与地下水的水化学组成中Na⁺为主要阳离子,补水后阴离子以HCO₃^-为主,淀区南部地表水电导率高;补水后地表水与地下水Ca²⁺、Mg²⁺和HCO₃^-浓度显著增加,水体电导率降低.（2）补水前地下水为Na-HCO₃型水,地表水主要为Na-Cl·SO₄及Na-Cl·HCO₃类型;补水后地表水与浅层地下水向Ca·Mg-HCO₃型演化,深层地下水水化学类型基本保持不变.（3）生态补水使白洋淀水位升高,淀区水面积增大,缓解了水资源短缺的问题;同时也使浅层地下水水化学组成发生改变,而深层地下水暂未受到影响.生态补水后,受稀释和混合作用的影响,水体Na⁺、Cl^-和SO₄^2-浓度显著下降,Ca²⁺、Mg²⁺及HCO₃^-浓度增加.在白洋淀生态补水中应"先治污,后补水",以减少补水过程中污染物向淀区的运移,还应注意区域地下水位上升过程中的阳离子交换及水岩相互作用,为合理调配生态补水及改善白洋淀生态环境提供科学依据.     

粤东五华河流域的化学风化与CO2吸收

基于对粤东五华河干流和支流水体的物理、化学组成测试数据,应用质量平衡法和相关分析法探讨湿热山地丘陵地区岩石化学风化过程对大气CO₂的吸收.结果表明:五华河水体的总溶解性固体含量(77.11 mg/L)接近于世界河流的平均值(65 mg/L);离子组成以Ca²⁺、Na⁺和HCO₃^-为主,可溶性Si次之.五华河流域化学径流组成主要源自硅酸盐矿物化学风化过程的贡献,碳酸盐矿物的贡献较少;大气和土壤CO₂是流域内岩石化学风化的主要侵蚀介质.与同一气候带其他河流相比较,五华河流域岩石化学风化过程对大气CO₂的吸收通量(2.14×105mol/(km²·a))较低,这主要是由于流域内缺乏碳酸盐岩所导致.     

南极洲万达盐湖水中方解石饱和指数的垂直变化及其控制因素

南极洲万达盐湖为饱和方解石湖水。计算出的方解石饱和指数随水深增加而变化。在Ca²⁺及HCO₃^-活度值均一的上部氧化环境湖水中,pH及溶解氧(DO)是控制该变化的主要因素,在下部还原环境湖水中,Ca²⁺及HCO₃^-的活度对方解石的饱和指数SI的变化起主要作用。这充分揭示了湖底部近代沉积物中分布较多方解石矿物的原因。     

夏季降雨事件对水库温室气体通量变化的影响:来自湖北官庄水库的高频观测

湖库淡水水域对温室气体排放的贡献不容小觑,然而观测时间的代表性不足以及缺乏对降雨因素的考虑制约了碳排放的准确估计.本研究以湖北宜昌境内官庄水库为例,选取强降雨多发的夏季时段,针对水气界面温室气体通量、水体表层和垂向剖面气体溶存浓度及环境因子开展了为期1周的原位高频观测,以探讨夏季降雨事件对水库温室气体通量变化的影响.结果表明,观测期内官庄水库水气界面CH₄通量变化范围为0.007~0.077 mg/（m²·h）,CO₂通量范围为5.48~57.57 mg/（m²·h）,白天和夜晚均表现为大气的碳源.小雨、中雨乃至暴雨天气条件下,CH₄和CO₂日均通量均较低,日通量倾向于受风速和温度调控.CH₄和CO₂通量变化趋势较为一致,观测期内日间排放量高于夜间排放量出现的次数更多,昼夜差异对降雨天气状况无明显响应,风速是CH₄和CO₂通量昼夜变化的主导因素.暴雨过程中,CH₄-k₆₀₀和CO₂-k₆₀₀与水气温差存在显著正相关,但水体垂向混合过程十分短暂.在平均雨强为3.8 mm/h的暴雨第I阶段,CH₄-k₆₀₀对风速和降雨的响应明显,而在雨强更大（8.5 mm/h）的第II阶段,CH₄-k₆₀₀与风速、降雨均未表现出相关性,通量箱在强降雨条件下的适用性可能存在雨强阈值.     

青藏盐湖卤水演化及资源

本文通过揭示宵蔵盐湖卤水在浓缩过程中成盐元素的行为以及卤水水化学炎型与PH值等的变化,得出结论如下：1.卤水中主要离子的演化方向是按Ca²⁺→Na⁺→K⁺→Mg²⁺→Ca²⁺（阳离子）和CO₃^2-→HCO₃^-→SO₄^2-→Cl^-（阴离子）顺序进行。2.除了析出固体外,微量元素一般在最后的浓缩卤水和析盐后的残余卤水中髙度富集。已査明盐湖卤水中有63种元素,其中钾、镁、硼、锂、铷、铯、铀、钍、稀土、氘已构成可以综合利用的宝贵资源。     

不同水文情景下洪泽湖二氧化碳排放通量特征及影响因素

内陆水域二氧化碳(CO₂)排放是全球碳平衡的重要组成部分,全球CO₂排放通量估算通常有很大不确定性,一方面源于CO₂排放数据观测的时空离散性,另一方面也是缺少水文情景与CO₂排放通量关联性的研究.本文观测了2018年洪泽湖不同水文情景表层水体CO₂排放通量特征,并探讨其影响因素.结果表明,洪泽湖CO₂排放通量为丰水期((106.9±73.4) mmol/(m²·d))>枯水期((18.7±13.6) mmol/(m²·d))>平水期((5.2±15.5) mmol/(m²·d)),且碳通量由丰(310.2~32.0 mmol/(m²·d))、枯(50.8~2.2 mmol/(m²·d))、平(-17.3~39.8 mmol/(m²·d))3种水文情景的交替表现出湖泊碳源到弱碳汇的转变,空间上CO₂排放通量总体呈现北部成子湖区低、南部过水湖区高的分布趋势.洪泽湖CO₂排放对水文情景响应敏感,特别是上游淮河流域来水量的改变,是主导该湖CO₂排放时空分异的重要因子.丰水期湖泊接纳了淮河更多有机和无机碳的输入,外源碳基质的降解和矿化显著促进了水体CO₂的生产与排放,同时氮、磷等营养物质的大量输入,加剧了水体营养化程度,进一步提高CO₂排放量,间接反映出人类活动对洪泽湖CO₂变化的深刻影响.平、枯水期随着上游淮河来水量的减少,驱动水体CO₂排放的因素逐渐由外源输入转变为水体有机质的呼吸降解.此外,上游河口区DOM中陆源类腐殖质的累积与矿化能够促进CO₂的排放,而内源有机质组分似乎并没有直接参与CO₂的排放过程.研究结果揭示了水文情景交替对湖库CO₂排放的重要影响,同时有必要进行高频观测以进一步明晰湖泊的碳通量变化及其控制因素.     

冰封期乌梁素海沉积物-水界面氨氮的交换特征

为揭示冰封期氨氮（NH₄⁺-N）在沉积物-水界面的迁移机制及内源性营养盐对全湖污染的贡献,于2018年2月初在乌梁素海湖区7个采样点采集了上覆水体与沉积物样品,得到了冰封期上覆水体与沉积物间隙水中的NH₄⁺-N浓度,估算了沉积物-水界面NH₄⁺-N的扩散通量.结果显示,上覆水体中NH₄⁺-N浓度变化范围为0.55~1.60 mg/L,平均值为1.05 mg/L,0~5 cm表层沉积物间隙水中NH₄⁺-N浓度是上覆水体中的10倍以上,其变化范围为6.64~18.63 mg/L,平均值为11.92 mg/L.估算沉积物间隙水NH₄⁺-N向上覆水体的扩散通量为1.282~4.269 mg/（m²·d）,表明在湖水冻结过程中,底泥沉积物接纳了大量的可溶性污染物成为内源污染源,会在冰封稳定期、融冰期和融冰后的一段时间内成为湖水的主要污染源.     

水库温室气体净通量评估模型(G-res Tool)及在长江上游典型水库初步应用

目前准确量化温室气体排放量已成为气候变化研究和政策制定的关键.在IPCC水库温室气体净通量的概念性框架下,国际水电协会汇总分析了全球223座水库的CO₂和CH₄研究成果,构建了G-res Tool,其可以用于评估已建或待建水库在长时间尺度下的温室气体净通量.本文介绍了G-res Tool模型的基本原理与模型框架,利用模型内置数据库中所涉及的中国长江上游12座典型水库数据进行初步应用分析,12座水库温室气体净通量平均值为88.17 g CO₂e/（m²·a）,在全球约7000座水库中所处水平为11.67%,处于低阈值范围.在水库温室气体净通量分析结果中,其他非相关人类活动产生的水库温室气体通量（UAS）在蓄水后总通量（Post）中所占比重远高于蓄水前温室气体通量（Pre）.长江上游水库蓄水后的CH₄和CO₂通量对于温室效应的贡献量相当.通过将G-res Tool模型蓄水后的温室气体通量评估结果和所涉及到的12座水库中已发表的数据对比分析发现,G-res Tool具有简便、适用面广等特点.但G-res Tool毕竟仍为经验性模型,其基本原理和模块设计上的内在缺陷在很大程度上限制了其应用范围并造成了一定的不确定性.对个案水库而言,长期跟踪观测与机理研究仍是未来减少水库温室气体净通量不确定性的关键.     

不同上覆水氟浓度对湖泊沉积物氟释放与微生物群落的影响

通过模拟沙湖沉积物-水系统,以沙湖原水氟离子（F^-）浓度为1倍浓度（0.69 mg/L）,设置0.5倍浓度、1倍浓度、1倍浓度灭菌、2倍浓度和4倍浓度共5个实验组,探究不同上覆水F^-浓度背景下沙湖沉积物中F^-的迁移.结果表明,沉积物F^-的释放量随上覆水F^-浓度的增加而呈下降的趋势,其中2倍和4倍浓度组的沉积物由释放F^-转变为吸附F^-.碱性水体有利于沉积物F^-的释放,即随着pH增大,F^-释放量也会增加.微生物的Beta多样性层次聚类分析表明,F^-会抑制Paenisporosarcina与Thiobacillus的相对丰度,但对Fusibacter的生命活动具有促进作用.根据各浓度组间优势菌属相对丰度与环境因子的冗余分析可得,Acinetobacter、Thiobacillus相对丰度与pH呈负相关;Fusibacter相对丰度与F^-浓度呈显著正相关,而Thiobacillus的相对丰度则与F^-表现出弱负相关.通过对各浓度组中重要离子的分析发现,0.5倍组和4倍组中F^-的迁移受Ca²⁺、HCO₃^-和SO₄^2-浓度影响较大;相关性分析表明0.5倍浓度组的Ca²⁺、HCO₃^-浓度与F^-浓度呈极显著正相关,而4倍组中F^-浓度和Ca²⁺、HCO₃^-浓度呈负相关,SO₄^2-浓度和F^-浓度的相关性则是0.5倍组呈负相关,4倍组呈极显著正相关.本文在不同上覆水F^-浓度背景下全面探究了沙湖沉积物中F^-释放和迁移机理,为沙湖及其他含氟地表水的氟污染防治提供理论支持.     

Major ion geochemistry and nutrient behaviour in the mixing zone of the Changjiang (Yangtze) River and its tributaries in the Three Gorges Reservoir

Inorganic ions and nutrients were measured at different depths of the Xiangxi and Daninghe Rivers to explore the mixing processes of representative bays in the Three Gorges Reservoir (TGR). HCO₃⁻ and Ca²⁺ are the dominant ions. Carbonate weathering is the most important mechanism controlling the ion water chemistry; however, important differences exist between the main channel and its tributaries. Major ion levels in the TGR bays depend on hydrological mixing. Results show that the major ions of Ca²⁺, Mg²⁺, Na⁺, K⁺, Sr²⁺, SO₄²⁻ and Cl⁻ show chemically conservative behaviour during transit through the bays of the TGR. This means the ions can be used as tracers in the same way that salinity is used in estuaries to explore behaviour of other non‐conservative elements and to indicate specific source waters. In contrast, nutrients are not conserved in the mixing zone. The mixing of the main channel and tributaries and biological utilization in backwater reaches were the key factor controlling nutrient distributions in Xiangxi and Daninghe Bays. Copyright © 2010 John Wiley & Sons, Ltd.     

喀斯特地区梯级水库建造对水化学分布的影响

为深入了解河流梯级筑坝对喀斯特地区河流水化学分布的影响,于2017年1、4、7和10月别对乌江干流洪家渡水库(多年调节)、乌江渡水库(季调节)和索风营水库(日调节) 3个具有不同滞留时间的水库进行水样采集,分析入库水、坝前剖面水和下泄水的水化学特征,探讨河流梯级筑坝对水化学分布及风化速率估算的影响.研究结果表明:3个水库深层水比表层水HCO3-浓度分别高12.9%、5.5%和8.0%,Ca~(2+)浓度分别高15.9%、2.4%和8.5%.河流梯级筑坝一定程度上改变了水体水化学组成,从而影响碳酸盐岩风化速率估算.整体上,洪家渡水库、索风营水库和乌江渡水库的全年风化速率变化范围分别为:-1.7%～15.4%、-5.6%～1.1%和-0.3%～3.4%.河流筑坝作用对风化速率估算及主量离子浓度的影响:HCO_3~-与Ca~(2+)浓度分布均为:洪家水库乌江渡水库索风营水库,这与水体滞留时间长短规律一致,表明水体滞留时间影响着水化学的组成分布.同时水体离子浓度表现出明显的季节性差异,丰水期各水库变化率明显大于枯水期.上述结论表明喀斯特地区河流连续筑坝后水化学组成及分布特征发生了一定程度改变,影响流域化学风化速率的估算,且影响程度随水体滞留时间延长而增大,并受气温影响.因此,今后在估算流域风化速率及探究水化学空间变化时应对筑坝作用加以考虑,以便更加准确地评估喀斯特流域岩石风化在全球碳循环中的作用.     

Snow and stream-water chemistry of the Ganga headwater basin,Garhwal Himalaya,India

Abstract

Studies of the chemical composition of snowpack and stream water were carried out in a catchment having an area of 53km² (31°03′-30°55′N and 78°40′-78°51′E) in the Garhwal Himalaya, India. The dominant ions in the snowpack and stream water were Ca²⁺, Na⁺, NO^? ₃, SO^2- ₄ and HCO^? ₃. Solute patterns in the snowpack show preferential elution. Investigation of the chemical composition of stream water shows that meltwater changes its composition substantially as it passes through soil pathways to the stream. The groundwater flushing perhaps controls the chemical composition of meltwater in the early spring. However, in the period from July to September, the stream water carries the chemical signature of monsoonal precipitation.     

柴达本盆地沙下盐湖的卤水化学及矿物沉积特征——以察尔汗盐湖区北部外围地带为例

对柴达木盆地察尔汗盐湖区外围沙下盐湖的卤水及沉积进行了综合研究。沙下盐湖卤水化学组成与地表径流和开放性盐湖卤水之间存在明显的差异性,具有高Na⁺+Cl^-、低Mg²⁺+Ca²⁺+SO₄^2-、贫K⁺+CO₃^2-+HCO₃^-等特征。沙下盐湖析盐层位含有新生矿物并夹带碎屑矿物,其盐类矿物组合为:石盐+羟氯镁铝石+光卤石。25℃等温蒸发相图表明,其卤水演化方向往光卤石析出区迁移,在穿越上覆盖层通道中卤水发生的物理化学反应与独特的沉积特征,可以作为继续寻找沙下盐湖的指导。     

淮北临涣矿采煤沉陷区不同水体水化学特征及其影响因素

为研究淮北临涣矿采煤沉陷区不同水体的补给水源及溶质来源,在现场调查的基础上,系统采集丰水期、平水期、枯水期沉陷区积水、地表河水和浅层地下水样进行测试分析,采用Piper三线图、Gibbs图和因子分析方法,对不同水体水化学特征及其影响因素进行讨论.结果表明:地表水水体总溶解性固体(TDS)质量浓度表现为枯水期丰水期平水期,浅层地下水表现为枯水期平水期丰水期,地表水TDS质量浓度明显高于浅层地下水.地表水中主要阴阳离子为Na~+、Cl~-和SO_4~(2-),水化学类型主要为SO_4~(2-)-Cl~--Na~+型;浅层地下水离子以HCO_3~-、Ca~(2+)和Mg~(2+)为主,表现为HCO_3~--Ca~(2+)-Mg~(2+)型.结合Gibbs图和因子分析可知,地表水受蒸发作用、地表径流以及采煤活动等因素影响,浅层地下水在一定程度上体现出大气降水和地表水补给的特点,受岩石风化作用影响较为明显.     

Hydrogeochemical characteristics of surface water and groundwater in the karst basin,southwest China

Groundwater is a very significant water source used for irrigation and drinking purposes in the karst region, and therefore understanding the hydrogeochemistry of karst water is extremely important. Surface water and groundwater were collected, and major chemical compositions and environmental isotopes in the water were measured in order to reveal the geochemical processes affecting water quality in the Gaoping karst basin, southwest China. Dominated by Ca²⁺, Mg²⁺, HCO₃^? and SO₄^2?, the groundwater is typically characterized by Ca? Mg? HCO₃ type in a shallow aquifer, and Ca? Mg? SO₄ type in a deeper aquifer. Dissolution of dolomite aquifer with gypsiferous rocks and dedolomitization in karst aquifers are important processes for chemical compositions of water in the study basin, and produce water with increased Mg²⁺, Ca²⁺ and SO₄^2? concentrations, and also increased TDS in surface water and groundwater. Mg²⁺/Ca²⁺ molar ratios in groundwater decrease slightly due to dedolomitization, while the mixing of discharge of groundwater with high Mg²⁺/Ca²⁺ ratios may be responsible for Mg²⁺/Ca²⁺ ratios obviously increasing in surface water, and Mg²⁺/Ca²⁺ ratios in both surface water and groundwater finally tending to a constant. In combination with environmental isotopic analyses, the major mechanism responsible for the water chemistry and its geochemical evolution in the study basin can be revealed as being mainly from the water–rock interaction in karst aquifers, the agricultural irrigation and its infiltration, the mixing of surface water and groundwater and the water movement along faults and joints in the karst basin. Copyright © 2009 John Wiley & Sons, Ltd.     

Spatial characteristics and controlling factors of chemical weathering of loess in the dry season in the middle Loess Plateau,China

Hydrochemistry methods were used to decipher the weathering and geochemical processes controlling solute acquisition of river waters in the dry season in the middle Loess Plateau (MLP), one of the most severely eroded areas and turbid riverine systems in the world. River waters were neutral to slightly alkaline with pH varying from 7.6 to 9.6. The total dissolved solids decreased from northwest to southeast with a mean value of 804 mg/l, much higher than the global average and other large rivers in China. Ternary diagram showed that river waters were dominated by Na⁺, HCO₃^?, and Cl^? with the main water‐type of HCO₃^?–Cl^?–Na⁺. Saturation index values, Mg²⁺, Ca²⁺, and HCO₃^? analyses indicated the preferential Ca²⁺ removal by calcite precipitation. Gibbs plots and stoichiometry plots indicated that the dissolved solutes were mainly derived from rock weathering with minor anthropogenic and atmospheric inputs. Samples in the northwestern basin are also influenced by evaporation. A forward model of mass budget calculation showed that, owing to high soluble characteristics, evaporite dissolution was a major feature of river waters and contributed 41% to the total dissolved cations on average, while carbonate and silicate weathering contributed 28%,and 25% on average, respectively. Besides evaporite dissolution, cation exchange is also responsible for the high concentrations of Na⁺ in river water. Spatial variations showed that evaporite dissolution and silicate weathering were higher in the northern basin, whereas carbonate weathering was higher in the southern basin. Different from most rivers in the world, the physical erosion rates (varying from 117.7 to 4116.6 t/km²y) are much higher than the chemical weathering rates (varying from 3.54 to 6.76 t/km²y) in the MLP because of the loose structure of loess and poor vegetation in the basin. In the future, studies on comparison of water geochemistry in different seasons and on influence of different types of land use and soil salinization on water geochemistry, denudation rates, and water quality should be strengthened in the MLP. These results shed some lights on processes responsible for modern loess weathering and also indicate the importance of time‐series sampling strategy for river water chemistry. Copyright © 2016 John Wiley & Sons, Ltd.