水文过程对缙云山径流盐基离子变化特征的影响

通过选取缙云山针阔混交林(马尾松×四川大头茶)和常绿阔叶林(四川大头茶×四川山矾)内2个标准径流小区,结合野外观测和室内分析研究降雨及径流的化学性质径流盐基离子变化特征,为该地区水环境保护提供依据。结果表明:1)针阔混交林与常绿阔叶林中p H值变化趋势相同均为:地表径流壤中流大气降水。p H与降雨量之间存在显著相关关系。2)在大气降雨-地表径流-壤中流过程中,NH+4的地表径流及壤中流输出总量小于降雨输入量,表明了土壤对NH+4有一定的吸附持留能力。其他盐基离子径流输出量均高于大气降雨的输入量,且主要以壤中流输出为主,元素发生流失。从盐基离子总量来看,径流输出量均增加:针阔混交林(2.86 kg/hm2),常绿阔叶林(2.47 kg/hm2),说明在两种林分内养分均流失。(3)K+、Ca2+、Mg2+和Na+盐基离子输出量与径流量之间存在相关关系,随着径流量的增大径流输出量增加。而NH+4输出量与径流量之间的相关性不明显,说明了NH+4的变化除受径流量的影响外,可能还受微生物、季节等其他因素的影响。     

山东寿光不同种植年限设施土壤的酸化与盐渍化

以山东寿光不同种植年限设施菜地为对象,研究并分析了土壤的酸化与盐渍化状况,结果表明:设施菜地土壤pH值平均为6.86,全盐含量为2.47g.kg-1,与露天菜地、自然土相比有较明显的酸化与盐渍化现象;设施菜地在连续种植0-12.7a间,土壤pH值随种植年限增加而降低,12.7a后则出现随种植年限增加而升高的现象,土壤全盐含量则表现出与pH值相反的变化趋势,其发生变化的转折年限约为8.4a;设施土壤中的Na+,Mg2+,Cl-,SO24-含量随种植年限的变化均表现出与土壤全盐量相同的趋势,且与种植年限的相关性均达到显著水平,这4种离子含量的变化可能是导致土壤全盐量随种植年限变化的重要原因;从土壤盐分离子组成来看,设施菜地土壤主要以SO42-、Cl-、Ca2+为主,分别占全盐量的62.4%、10.6%、9.3%,设施菜地中SO24-、Cl-、Mg2+、Na+含量与全盐量均呈极显著相关,其中相关性程度最大的为SO24-(r=0.9291)和Mg2+(r=0.7224)。设施菜地中SO24-含量与pH值变化存在极显著相关(r=-0.5508),其大量累积可能是造成调查区域设施土壤酸化的重要原因。     

祁连山西水林区土壤阳离子交换量及盐基离子的剖面分布

以祁连山西水林区分布的棕钙土、灰褐土、栗钙土和高山草甸土为对象,研究了阳离子交换量和盐基离子(K+、Na+、Ca2+、Mg2+)的剖面分布规律及其与土壤理化因子的关系。结果表明:土壤阳离子交换量(CEC,介于4.80—48.10 cmol/kg)和盐基总量(TEB,介于4.67—21.34 cmol/kg)随剖面深度的增加逐渐减小,不同土壤类型的大小顺序为:灰褐土>高山草甸土>栗钙土>棕钙土;土壤盐基组成以Ca2+、Mg2+为主(占TEB的比例平均为71.6%、22.9%),K+、Na+所占比例较低(占TEB的比例平均为3.3%、2.2%);棕钙土、灰褐土和栗钙土盐基离子的剖面分布由浅至深呈现:K+≈Ca2+>Na+≈Mg2+,高山草甸土盐基离子则呈现:K+>Na+>Mg2+>Ca2+。不同土壤类型间盐基离子的含量及饱和度随发生层次不同存在较大差异。土壤有机质是CEC的主要贡献因素,粉粒对CEC也有显著的促进作用,而砂粒、CaCO3对CEC有显著抑制作用。土壤生物复盐基作用弱于淋溶作用,造成盐基饱和度较大(BSP,介于44.4%—97.2%),并随剖面深度的增加逐渐增大。相关性分析表明,土壤交换性Na+、Mg2+的含量及饱和度均呈极显著正相关,交换性Na+、Mg2+饱和度与CaCO3含量呈极显著正相关;pH值与BSP呈极显著正相关;土壤速效P含量与CEC呈极显著正相关,速效K含量与交换性K+含量呈极显著正相关。     

湖南韶山森林复合冠层沉降化学

在韶山森林设立了 1 0个 30m× 30m的样方 ,研究了 1年中各个季节的二维结构冠层在酸雨作用下各离子的净沉降及森林地表接收的总酸沉降的变化。结果表明 ,来源于树冠层叶中营养离子的洗脱与大气中含钙颗粒物质的Ca2 + 的净沉降在乔木冠层和灌木亚冠层都为正 ,Mg2 + 除了在生长季节外 ,其冠层仍有较明显的滤出现象 ,K+ 在乔木冠层树冠的大量的滤出与灌木亚冠层的摄入形成明显对比。SO42 -,NO3 -,Cl-在秋冬两季树冠层均有较强的洗脱现象 ,而海洋输送则成为Cl-的另外一个重要来源。总酸沉降结果表明 ,盐基离子中Ca2 + 在春夏两季沉降量最大 ,Mg2 + 的沉降则以秋冬两季的量最高 ,K+ 的最大沉降量出现在秋季。     

大气氮沉降对阔叶林红壤淋溶水化学模拟研究

在氮饱和的森林生态系统中,氮沉降的增加将导致NO3-淋溶的增加及土壤酸度的提高,从而影响土壤质量及林业的可持续发展。然而,大气氮沉降对我国南方红壤地区森林生态系统中土壤的影响研究还很少,尤其是氮沉降引起的土壤淋溶液化学组成方面。研究中,以中国科学院红壤生态实验站林草生态试验区阔叶林红壤为对象,在恒温(20℃)条件下,通过土壤淋洗柱(直径10cm、高60cm)进行了8个月间隙性淋溶试验,来模拟研究不同氮输入量(0、7.8、26mg月-1.柱-1和52mg月-1柱-1)对阔叶林红壤NO3-、NH4 、SO42-、H 和土壤盐基离子(Ca2 、Mg2 、K 和Na )的淋溶和土壤酸度的影响。结果表明,随氮输入量增加,淋溶液中NO3-、EC、H 和总盐基离子逐渐增加,但淋溶液中无NH4 。不同氮处理时,土壤有机氮总表观矿化量分别为189.6、263.9、372.8mg月-1.柱-1与554.2mg柱-1,氮输入明显促进了土壤有机氮的矿化,且土壤有机氮的表观矿化量与氮输入量间呈正线性相关(R2=0.997**)。无氮(0mg月-1柱-1)、低氮(7.8mg月-1柱-1)、中氮(26mg月-1柱-1)和高氮(52mg月-1柱-1)输入处理下,土壤交换态盐基淋溶总量分别占土壤交换性盐基总量的13.6、18.4、27.7%和48.1%。不同的盐基离子对氮输入的反应不同,Ca2 和Mg2 淋溶量随氮输入量的增加而增加,对Na 和K 则无明显影响。土壤交换态离子中随淋洗液输出最多的为Ca2 (无氮、低氮、中氮和高氮输入处理的土壤交换态输出量占土壤交换态的比例分别为22.6、31.4、46.7%和82.5%),其次为Na (无氮、低氮、中氮和高氮输入处理的土壤交换态输出量占土壤交换态的比例分别为16.0、10.7、17.6%和26.3%),最少的为Mg2 (无氮、低氮、中氮和高氮输入处理的土壤交换态输出量占土壤交换态的比例分别为5.0、6.9、11.1%和16.9%),几乎没有土壤交换性K 输出。与对照相比,有氮处理后土壤中硫酸根离子的淋失量明显减少(p<0.05)。表层土壤pH值随氮输入量的增加而显著下降,各处理间差异极显著(p<0.01)。可见,大气氮沉降的增加将加速阔叶林红壤的养分淋失和土壤酸化的程度。     

广州流溪河降水化学成分及其海洋源分析

通过2006年6月～2008年5月在广州流溪河地区采集的106次降雨水样(雨量范围0.7～268.6 mm)及其化学测试,论述了几类主要离子在降水中的含量特征、季节变化、物质的海洋来源以及雨水中离子平衡等.结果显示:(1)流溪河周边没有明显的点污染源,但酸雨降水量占总降水量的69.5%,说明降水中的污染物来自该地南部和北部污染区的中距离传输;如夏季和秋季时,台风等海洋气流把珠三角南部更多的NOx传输至该地,使得雨水中NO-3含量在夏季和秋季最大.(2)降水中的年平均F-、Cl-、NO-2、NO-3、PO3-4、SO2-4、NH+4、Ca2+、Mg2+、K+、Na+和Al3+离子浓度分别为3.76、22.80、0.45、25.22、0.86、62 9、41.5、35.77、2.93、5.45、14.8和0.943 μeq·L-1;且单个降水事件中的离子浓度大小与降水量呈负相关.(3)流溪河雨水酸度主要来自SO2-4、NO-3和Cl-1,且主要靠中和因子较大的NH+4、Ca2+、K+等阳离子起缓冲作用;该地降水沉降中的强酸酸量为2 053 keq hm-2 a-1,NH+4、Ca2+、K+、Mg2+、Al3+的缓冲量分别为0.865、0.745、0.114、0.061、0.020 keq hm-2 a-1.(4)降水化学的月和季节波动明显,酸雨主要集中于雨季,而旱季雨水酸度较低,这和重庆及北京的情况相反.(5)在雨水中化学成分Na+全部来源海洋的假设前提下,分析得出:绝大部分Mg2+和部分Cl-(80.07%)、SO2-4(2.91%)、Ca2+(1.86%)、K+(6.19%)来自于海洋,而F-、NO-3来自海洋的贡献率非常小,可以忽略不计.     

Responses of exchangeable base cations to continuously increasing nitrogen addition in alpine steppe: A case study of Stipa purpurea steppe

土壤交换性盐基离子(Ca ²⁺、Mg ²⁺、K ⁺、Na ⁺)在维持土壤养分与缓冲土壤酸化中起着重要作用, 了解其对氮添加的响应有助于准确评估氮沉降背景下生态系统结构与功能的动态变化。然而, 目前关于土壤交换性盐基离子对氮添加响应的相关研究主要集中在酸性土中。鉴于目前在碱性土中研究相对较少的现状, 该研究以青藏高原高寒草原为研究对象, 依托氮添加控制实验平台, 通过连续3年(2014-2016)的测定, 考察了8个不同施氮水平(0、1、2、4、8、16、24、32 g·m ^-2·a ^-1)下土壤交换性盐基离子含量变化及其可能原因。结果显示: 随着施氮量的增加, 土壤交换性盐基离子, 尤其是Mg ²⁺与Na ⁺含量显著降低。并且, 盐基离子含量与植物地上生物量显著负相关(p < 0.05), 说明氮添加通过促进植物生长, 加速植物对盐基离子的吸收, 进而导致土壤中盐基离子含量降低。此外, 盐基离子含量也与土壤无机氮含量呈显著负相关(p < 0.05)关系, 说明施氮还通过提高土壤中无机氮含量进而导致更多NH₄ ⁺与土壤吸附的盐基离子交换, 同时加剧NO₃ ^-淋溶, 带走等电荷阳离子。需要指出的是, 虽然连续施氮导致土壤pH值下降, 但该土壤目前仍处于碳酸盐缓冲阶段, 说明通常在酸性土中报道的“因缓冲土壤酸化引起的盐基离子损失机制”在碱性土中并不成立。这些结果意味着持续的氮输入会造成碱性土中盐基离子损失, 进而影响土壤缓冲能力与植被生产力, 未来草原生态系统管理中应重视这一问题。     

茂兰喀斯特地区森林降水分配的水化学特征

于2007年9月—2009年8月对中国西南茂兰喀斯特地区亚热带常绿落叶阔叶混交林大气降水、林冠穿透雨和树干茎流进行观测,分析了各降水分配中的养分离子(Ca2+、Mg2+、K+、Na+、NH4+、SO42-、NO3-、Cl-)浓度动态变化规律及年养分元素输入量。结果表明:7—9月,林外雨、林冠穿透雨和树干茎流中各养分离子浓度相对较低,12月—翌年2月,各降水分配中各养分离子浓度相对较高;降水通过林冠或树干后,除了Na+浓度无显著变化外,NH4+浓度表现下降趋势,Ca2+、Mg2+、K+、Cl-、NO3-和SO42-均表现增加趋势;林外雨的养分元素输入量顺序为Ca2+SO42--SNH4+-NCl-K+Na+Mg2+NO3--N。在林冠穿透雨+树干茎流中的养分元素输入量顺序为K+Ca2+Cl-SO42--SMg2+NH4+-NNO3--NNa+。与非喀斯特地区相比,林外雨中的各养分离子浓度较低,林冠穿透雨、树干茎流中的K+、Ca2+、Mg2+增加幅度较大。总体来看,独特的立地特征决定了该地区Ca2+、Mg2+的积极参与生态系统养分循环和K+高效循环的特征。     

CO2浓度升高对毛竹器官矿质离子吸收、运输和分配的影响

为了给大气CO2浓度逐渐升高背景下的毛竹林适应性经营管理提供理论依据,运用开顶式气室(OTCs)模拟大气CO2浓度升高(500、700 μmol/mol)情景,以目前环境背景大气为对照,研究了Na+、Fe2+-Fe3+、Ca2+、Mg2+等矿质离子在毛竹器官中吸收、运输和分配的变化规律.结果显示,除CO2浓度700 μmoL/mol对Ca2+浓度在毛竹器官中大小排序会产生影响外,CO2浓度500、700 μmol/mol并未改变毛竹器官中Na+、Fe2+,Fe3+、Mg2+、Ca2+浓度的大小排序.CO2浓度升高对竹叶Fe2+-Fe3+和竹枝Fe2+-Fe3+、Mg2+浓度无明显影响,但对器官的其它矿质离子浓度会有不同程度的影响,竹叶Ca2+和Mg2+、竹枝Na+和Ca2+、竹秆Na+和Ca2+及Mg2+、竹根Na+和Mg2+浓度明显提高,竹叶Na+、竹秆Fe2+-Fe3+、竹根Fe2+-Fe3+和Ca2+浓度明显降低;随着CO2浓度的升高,竹叶Fe2+-Fe3+/Na+、Mg2+/Na+和Ca2+/Na+,竹枝Ca2+/Mg2+及各器官Mg2+/Fe2+-Fe3+、Ca2+/Fe2+-Fe3+均逐渐增大,而竹枝、竹秆、竹根Fe2+-Fe3+/Na+、Mg2+/Na+、Ca2+/Na+和竹叶、竹秆、竹根Ca2+/Mg2+均逐渐减小;CO2浓度升高后除竹根-竹秆Sca.Na、竹秆-竹枝SMg,Fe和竹枝-竹叶Sca,Mg明显下降外,其余的毛竹器官矿质离子向上运输系数变化平缓或明显提高.研究表明CO2浓度升高增强了毛竹立竹根部积累Na+能力和Fe2+-Fe3+、Ca2+和Mg2+的向上选择性运输能力,提高了光合器官竹叶中矿质养分元素浓度,可维持体内矿质养分元素平衡,有利于提高毛竹对高浓度CO2环境的适应能力.     

成都市冬季不同粒径大气颗粒物水溶性无机离子的变化特征

利用Anderson冲击式分级采样器,在2010年冬季采集了成都市城东区不同粒径的大气颗粒物样品,分析了9种水溶性离子(SO42-、NO3-、Cl-、F-、NH4+、Ca2+、Mg2+、K+、Na+)的含量,并探讨其分布变化特征.SO42-、NO3-、NH4+、Cl-、K+、Na+等离子主要集中在粒径为3.3～0.65μm的细颗粒物中,而Ca2+、Mg2+则集中在粒径为11 ～4.7μm的粗颗粒物中.SO42-、NO3-、NH4+、Ca2+是主要的无机离子;在不同天气条件下,5O42-、NO3-的质量浓度按雾天、阴天、雨天递减,且雾天较阴天高2.5倍左右,较雨天高5倍左右,而其他离子也高出2倍左右;在不同粒径颗粒物中[NO3-]/[SO42-]比值均较小(＜1),说明成都市目前仍然以固定(燃煤)污染源为主,移动污染源(汽车尾气)的影响正逐步增强.     

Long-term and seasonal changes in the chemical composition of precipitation and surface waters of lakes and tarns in the English Lake District

SUMMARY. The composition of bulk (wet and dry) precipitation in 1975 and 1976 was similar to that found 22 years previously. In 1975, mean values for nine precipitation samplers at one site (Wraymires) ranged from pH 4.3 to 4.5; similar values were obtained in 1976. Samplers covered with fine-mesh plastic gauze caught substantially more Ca²⁺ and K⁺ than open samplers, but pH and SO^2-₄+ NO₃^- concentrations were similar in open and covered samplers. In precipitation, c. 50% of H⁺ was balanced by NO₃^- and c. 50% by SOi; 80% of the SO^2-₄ was balanced by Ca²⁺ and Mg²⁺. Conccntrations of major cations (H⁺, Na⁺, K⁺,Ca²⁺, Mg²⁺) and anions (CI^-, NO₃^- SO^2-₄ and alkalinity [Alk—largely HCO₃^-]) in upland water- bodies were similar to those found in precipitation, but pH levels were generally higher and above 6.0 m some tarns. At lower altitudes, on base-rich roeks and soils, Ca²⁺ and Alk become dominant. Results of a survey of lakes and tarns in 1974–78 are compared with a survey in 1953–56 and published data (chiefly for pH and Alk) for 1947–50, 1932 and 1928. Comparisons are also made with other measurements of Alk in three productive lakes (Blelham Tarn, Esthwaite Water and Windermere) for 1936–39 and 1945–80. Winter levels of NO₃-N, PO₄-P and Si are given for these lakes; although the first two have increased during the late 1960s and the 1970s there has been no significant change in the last. NO₃^- and probably some SO^2-₄. In productive lakes a substantial (c. 50%) rise in mean Alk occurred during the late 1960s and the 1970s, possibly related to increased winter levels of NO₃-N and PO₄-P derived from sewage and fertilizers. In this period the maximum pH levels reached in summer were notably high, sometimes exceeding pH 10. The rise in Alk, conductivity and pH of surface waters is influenced by climatic factors (a decade of drier years), sewage input and biological productivity within the lakes. Considerable seasonal fluctuations in the concentrations of major ions, a characteristic feature of surface waters in the English Lake District, are illustrated and some implications for cation-anion balance briefly discussed. Mid-winter concentrations are usually high forNa⁺, K⁺, Cl^-. NO₃^-and low for Ca²⁺, Mg²⁺, Alk. SO^2-₄. Alkalinity. pH and conductivity of Lake District tarns and lakes show no signs of acidification during the period 1928–80. On the contrary, productive lakes have become more alkaline and some unproductive low-alkalinity (< 100 μ-equiv. 1^-1) lakes also show signs of alkalization, with increased mean concentrations of Na⁺. Ca²⁺ and Mg²⁺, balanced by Alk.     

基于典范对应分析的滨海湿地土壤季节性盐渍化特征

为了更好地开发利用黄河三角洲湿地土壤资源和生态环境建设,运用单因素方差分析(One-way ANOVA)和典范对应分析方法(CCA),对黄河口湿地0—10 cm土壤全盐量(TS)、盐分离子组成、pH、钠吸附比(SAR)、电导率(EC)的季节性变化特征及数量关系进行了分析。结果表明:该区土壤属于盐土类型,春季(5月)、夏季(8月)、秋季(10月)全盐含量均高于17.9 g/kg,且春季、秋季的含盐量高于夏季,造成春、秋季积盐,夏季脱盐。盐分阳离子以Na~+为主,阴离子以Cl~-为主,除Mg~(2+)在夏季、秋季和Cl~-在秋季表现出强烈的变异性外,其余离子在不同季节均表现出中等强度的变异性。春季,Cl~-与Na~+、Mg~(2+),SO■与K~+;夏季,Cl~-与HCO~-_3,SO■与Mg~(2+)、Ca~(2+),Ca~(2+)与Mg~(2+);秋季,Cl~-与SO■,SO■与Mg~(2+),Ca~(2+)与Mg~(2+),均有很好的关联性。pH值均介于7.7—8.1之间,各个季节受盐分离子的影响较小,分布较为均匀。SAR介于3.08—5.29之间,春季受控于HCO~-_3;夏季受控于K~+;秋季受各离子的影响均较小,分布较为均匀。EC介于7.16—13.04 mS/cm,春季受各离子的影响均较小,其空间分布较为均匀;夏季受控于SO■、Ca~(2+)、Mg~(2+);秋季受控于Na~+。TS与Cl~-、Na~+、Mg~(2+)在季节变化上的差异性一致,且各个季节均受控于Cl~-。故通过合理的措施控制或减少Cl~-来源是一条减轻黄河口湿地土壤盐渍化的合适途径。     

黄河口湿地柽柳灌丛土壤盐渍化特征

为探究黄河三角洲湿地柽柳灌丛下土壤的盐渍化特征,在黄河三角洲国家级自然保护区(37°35''-12''N,118°33''-119°20''E)黄河入海口附近,根据长势基本一致的原则分别在碱蓬群落、柽柳群落和芦苇群落各选3株柽柳,采集柽柳灌丛下土壤样品,分析土壤盐分和盐碱化参数的空间分布以及距基茎不同距离处研究对象(土壤总盐(TS)、电导率(EC)、pH、交换性钠百分率(ESP))和环境因子(Na⁺、K⁺、Ca²⁺、Mg²⁺、Cl^-、HCO₃^-、SO^2-₄)之间的关系。结果表明：(1)研究区土壤为弱碱化盐土,离子含量由高到低依次为Cl^->Na⁺>SO^2-₄ >Ca²⁺>Mg²⁺>HCO^-₃>K⁺。除pH在土壤表层数值最低外,表层土壤TS、EC、ESP和盐分离子大于深层土壤,显示表聚性。(2)土壤盐分和盐碱化参数空间分布总体为：在柽柳基茎周围形成"盐谷"、"碱谷"效应, Na⁺、Mg²⁺、Cl^-表现为"盐谷",K⁺ 、SO^2-₄ 、Ca²⁺ 表现为"盐岛"。(3)在整个土壤剖面中,与TS、EC相关性最强的阴阳离子为Mg²⁺、Cl^-,从灌丛中心到灌丛间裸地Ca²⁺、SO^2-₄与TS、EC的相关性逐渐减弱,Mg²⁺、Cl^-与TS、EC的相关性逐渐增强。Ca²⁺和SO^2-₄与pH表现为较强的负相关性;与ESP相关性最强的阴离子为HCO^-₃,与之相关性最强的阳离子为Na⁺和K⁺,并且Na⁺和K⁺与ESP的相关性表现出从灌丛中心向外逐渐增强。(4)土壤盐渍化主要受控于Na⁺,从灌丛下到灌丛间裸地Cl^-对盐渍化程度的影响逐渐增加,SO^2-₄的影响逐渐降低。     

杨树人工林生态系统降水再分配及主要离子特征

大气降水是森林生态系统养分输入的主要途径之一,对养分的生物地球化学循环有着重要的意义。对13年生杨树人工林林外雨、树干流、林内雨和地表径流等水文过程中的养分特征进行了调查分析,旨在了解该生态系统的养分输入与输出规律,为杨树人工林可持续经营提供依据。结果表明,从2013年11月至2014年10月,杨树人工林生态系统林外雨量为1154.1 mm,树干流量仅占大气降水量的2.3%,15.4%的大气降水被杨树人工林的冠层截留;林内雨、树干流与大气降水量(林外雨)的动态变化规律相似。各类降水年加权平均pH值表现为林内雨林外雨树干流;各类降水的离子浓度动态变化规律基本一致,即在降水量较小的11月至次年1月份,各阴阳离子的浓度普遍较高,在降水量较大的2—9月份,阴阳离子浓度普遍较低。SO_4~(2-)-S和Ca~(2+)分别是各类降水中的主要阴离子和阳离子;整体上,树干流的离子浓度林内雨大气降水;林内雨是养分输入的主要形式,通过林内雨输入林地较多的养分离子是Ca~(2+)和K~+,分别为70.83 kg hm~(-2)a~(-1)和63.31 kg hm~(-2)a~(-1);地表径流和土壤渗漏是养分输出的主要形式,输出林地较多的离子是Cl~-和Ca~(2+),分别为196.47 kg hm~(-2)a~(-1)和123.09 kg hm~(-2)a~(-1),其次为SO_4~(2-)-S、Mg~(2+)、Na~+、K~+;NH_4~+-N和NO_3~--N的输出量不足输出离子总量的1%。所以,从水文过程看,杨树人工林生态系统无机氮(NH_4~+-N和NO_3~--N)和K~+表现为净积累,净积累量分别为10.9 kg hm~(-2)a~(-1)和56.4 kg hm~(-2)a~(-1),其他离子表现为净损失,其中Cl~-的净损失量达179.8 kg hm~(-2)a~(-1)左右,其他离子损失量50 kg hm~(-2)a~(-1)。     

凋落物和根系输入对南亚热带季风常绿阔叶林土壤养分的影响

植被凋落物和根系输入在调节森林土壤元素生物地球化学循环中扮演着关键作用。目前仍然不清楚凋落物和根系输入对热带原始林土壤主要元素含量的调控作用。针对该研究现状,以中国南亚热带季风常绿阔叶林为研究对象,通过开展凋落物与根系输入改变的控制试验（6个处理,每处理4次重复：对照、凋落物加倍、凋落物去除、断根、断根+凋落物加倍、断根+去除凋落物）,探讨了凋落物和断根处理对土壤可溶性离子、土壤酸中和能力（ANC）和阳离子交换量（CEC）的短期影响。凋落物与根系处理半年后的结果显示：（1）凋落物去除与加倍处理都显著增加了0-40 cm土壤NO₃^-含量,并且凋落物去除效应大于添加效应;去除凋落物增加了表层土壤（0-20 cm） Ca²⁺、Mg²⁺、Na⁺的含量。（2）断根处理显著增加0-40 cm土壤NO₃^-和表层土壤Ca²⁺、Mg²⁺含量。（3）断根和去除凋落物交互处理显著增加了0-40 cm土壤NO₃^-和表层土壤Ca²⁺、Mg²⁺、K⁺含量,产生了叠加效应。（4）凋落物和断根处理并没有改变土壤pH,但降低了土壤酸中和能力（除凋落物加倍外）,其降低的原因主要与阳离子交换量的降低和NO₃^-含量的增加有关。这些结果表明,土壤养分离子的可利用性（尤其是NO₃^-和Ca²⁺、Mg²⁺）和酸缓冲能力对凋落物和根系输入改变响应敏感,森林植物及其凋落物对土壤养分保留和缓冲性能具有重要调节作用。在人为干扰和气候变化加剧背景下,该研究可为森林生态系统可持续管理提供重要的理论参考。此外,植被凋落物和根系输入改变引起的长期生态学效应仍值得进一步关注。     

Alkalinity and acidity cycling and fluxes in an intermediate fen peatland in northern Ontario

Peatlands are important to global carbon (C) sequestration and surface water acid–base status, both of which are affected by peatland alkalinity and acidity cycling. Relationships among sulfate (SO₄ ^2?), nitrate (NO₃ ^?), organic acids (OA^?), base cations (i.e., Ca²⁺, Mg²⁺, K⁺, and Na⁺), proton (H⁺) acidity, and bicarbonate (HCO₃ ^?) alkalinity were investigated in an intermediate fen peatland in northern Ontario during 2004 (an average precipitation year) and 2005 (a dry summer). Potential evapotranspiration was higher and the water table, groundwater input from the uplands, and runoff were lower during 2005. Net inputs of base cations, HCO₃ ^?, SO₄ ^2?, and OA^?, and to a lesser degree NO₃ ^?, were lower during the drier year, mainly due to lower groundwater transfer to the fen. Fen porewater HCO₃ ^? concentration and net output were also lower in the drier year, whereas Ca²⁺, Mg²⁺, and SO₄ ^2? concentrations and net output were higher. During the climatically average year, N immobilization, carbonic acid (H₂CO₃) dissociation, and OA dissociation were equally important H⁺-producing reactions. Peat cation exchange accounted for 50% of the H⁺ sink, while SO₄ ^2? reduction and denitrification accounted for an additional 20 and 25% of the H⁺ sink, respectively. During the dry year, S oxidation accounted for 55% of the H⁺ net production, while that for H₂CO₃ dissociation was 70% lower than that during the climatically average year. Peat cation exchange consumed three times the acidity, and accounted for 92% of the H⁺ consumption during the dry year compared to the climatically average year. This was consistent with a three-fold higher net base cation export from the fen during the dry year. Based on the study results, a conceptual model was developed that describes the role of acidity formation and its implications to intermediate fen acidification.     

Plant induced alteration in the rhizosphere and the utilisation of soil heterogeneity

Plant-soil interactions result in a special rhizosphere soil chemistry, differing from that of the bulk soil found only a few mm from the root. The aim of this study was to investigate adaptation mechanisms of herbs growing in acid soils through studying their rhizosphere chemistry in a greenhouse experiment and in a field study. Ten herbs were grown in acid soil (pH 4.2 in the soil solution) in the greenhouse. The concentrations of NO₃ ^-, SO₄ ^2-, phosphates, Ca²⁺, Mg²⁺, Mn²⁺, K⁺, Na⁺, NH₄ ⁺ and pH were analysed in soil solutions obtained by centrifugation. The general pattern found was a depletion of nutrients in the rhizosphere compared with their concentrations in the bulk soil. The pH increase (up to 0.7 units) in the rhizosphere soil appeared to be caused by plant uptake of NO₃ ^- (r²=0.88). The ion concentrations in the soil solution of the rhizosphere were dependent on plant species and biomass increase. Although species with a larger biomass and higher growth rates showed a higher degree of ion depletion (except for Na⁺, SO₄ ^2-) in the rhizosphere, there were also species specific responses. A field study of five herbs at five oak forest sites in Southern Sweden (Scania) was also carried out. In addition to the soil solution concentrations, the loss on ignition (LOI) and the concentrations of 0.1 M BaCl₂ extractable K⁺, Mg²⁺, Mn²⁺, Ca²⁺, and Al ions were measured. The amount of soil solution Al was determined as free ionic (quickly reacting) Al. For all species and sites, the LOI and the concentrations of exchangeable cations were higher in the rhizosphere than in the bulk soil, apparently due to the roots preferably growing at organic-rich microsites. The concentrations of the ions as measured in the centrifuged soil solution, were either higher in the rhizosphere than in the bulk soil or were the same in both, except for NO₃ ^- and quickly reacting Al. The lower concentrations of quickly reacting Al in the rhizosphere, compared with the bulk soil could indicate the uptake of Al by the plant or the exudation of complexing substances. The pH differences were only small and mostly non-significant. Plant-soil interactions and the ability of plants to utilise heterogeneity of the soil appear to be more important for plant growth in acid soils than recognised heretofore. Rhizosphere studies provide an important means of understanding plant strategies in acid soils. This revised version was published online in June 2006 with corrections to the Cover Date.     

The Occurrence,Sources and Spatial Characteristics of Soil Salt and Assessment of Soil Salinization Risk in Yanqi Basin,Northwest China

In order to evaluate the soil salinization risk of the oases in arid land of northwest China, we chose a typical oasis-the Yanqi basin as the research area. Then, we collected soil samples from the area and made comprehensive assessment for soil salinization risk in this area. The result showed that: (1) In all soil samples, high variation was found for the amount of Ca²⁺ and K⁺, while the other soil salt properties had moderate levels of variation. (2) The land use types and the soil parent material had a significant influence on the amount of salt ions within the soil. (3) Principle component (PC) analysis determined that all the salt ion values, potential of hydrogen (pHs) and ECs fell into four PCs. Among them, PC1 (C1^-, Na⁺, SO₄ ^2-, EC, and pH) and PC2 (Ca²⁺, K⁺, Mg²⁺and total amount of salts) are considered to be mainly influenced by artificial sources, while PC3 and PC4 (CO₃ ^- and HCO₃ ^2-) are mainly influenced by natural sources. (4) From a geo-statistical point of view, it was ascertained that the pH and soil salt ions, such as Ca²⁺, Mg²⁺ and HCO₃ ^-, had a strong spatial dependency. Meanwhile, Na⁺ and Cl^- had only a weak spatial dependency in the soil. (5) Soil salinization indicators suggested that the entire area had a low risk of soil salinization, where the risk was mainly due to anthropogenic activities and climate variation. This study can be considered an early warning of soil salinization and alkalization in the Yanqi basin. It can also provide a reference for environmental protection policies and rational utilization of land resources in the arid region of Xinjiang, northwest China, as well as for other oases of arid regions in the world.     

黑河天涝池流域典型林分生态水文化学特征

采集了黑河天涝池流域典型林分林外雨、穿透雨、树干径流和枯透水,并检测水体pH值和12种离子(K~+、Ca~(2+)、Na~+、Mg~(2+)、NH_4~+、Cu~(2+)、Zn~(2+)、Pb~(2+)、Cd~(2+)、Cl~-、SO_4~(2-)、NO_3~3)的质量浓度。结果表明:天涝池流域大气降水pH均值为7.74,呈碱性,降水中离子绝对质量浓度较低,最高的是NO_3~-,质量浓度为1.1111 mg/L,最低的为Na~+,质量浓度为0.0108 mg/L;两种林分冠层有降低降雨pH值的作用,青海云杉林冠层对NH_4~+有升高作用,祁连圆柏林冠层对NH_4~+有降低作用,两种林冠层对NO_3~-和Cu~(2+)质量浓度有降低作用,对其它离子质量浓度均表现为升高作用;两种林分树干径流有提高穿透雨pH值的作用,与穿透雨相比,两种林分树干径流中阴离子均有升高,圆柏树干径流中所有阳离子质量浓度均有下降,云杉树干径流中Ca~(2+)、K~+、Mg~(2+)和Na~+减少,NH_4~+和Cu~(2+)增加;典型林分枯透水有提升穿透雨pH值的作用,与穿透雨相比,两种林分枯透水中阴离子质量浓度均有升高,云杉枯透水各阳离子均有降低,圆柏枯透水中Ca~(2+)、K~+和Mg~(2+)质量浓度升高,NH_4~+、Na~+和Cu~(2+)质量浓度下降;在采集的所有样本中,Pb~(2+)和Cd~(2+)均未检出,而Zn~(2+)仅在云杉树干径流中检出。     

Atmospheric deposition, mass balances, and processes regulating streamwater solute concentrations in mixed-conifer catchments of the Sierra Nevada, California

Solute concentrations in atmospheric deposition and stream water were measuredfrom 1984 through 1993 to determine the fate and mobility of solutes in twogauged mixed-conifer catchments (Tharp's and Log creeks) located in theSierra Nevada, California. The two catchments contain mature forest standsdominated by Abies concolor (white fir), Sequoiadendron giganteum (giantsequoia), Abies magnifica (red fir) and Pinus lambertiana (sugar pine).Ammonium, Cl^-, Ca²⁺ and NO^- ₃were highest in concentration of the solutes measured in wet deposition;bulk deposition was highest in SO^{2- 4}, NH⁺ ₄,Cl^- and H⁺. Net retention ofH⁺, NO₃ ^-, NH₄ ⁺,SO₄ ^2- and Cl^- occurred in both catchments.Discharge was dominated by spring snowmelt with the largest export yieldsfor acid neutralizing capacity (ANC), SiO₂, andCa²⁺. Export yields of H⁺,NO₃ ^-, NH₄ ⁺ and PO₄ ^3-were relatively small (0.5 kg ha^-1 y^-1).Discharge-concentration relationships for ANC, SiO₂,Na⁺, K⁺, Ca²⁺ andMg²⁺ were inverse and their concentrations in stream waterwere primarily influenced by discharge and annual differences in the relativecontributions of snowmelt and groundwater. The mobility of these solutes iscontrolled by the rates of mineral weathering and ion exchange. The positiverelationship of SO₄ ^2- concentration with increasingdischarge suggests that atmospherically deposited SO₄ ^2-is temporarily stored and that its release is controlled by the extent of soilwater flushing.