泥炭沼泽不同植物群落中地表糙度变化及其影响机制

对藏南沉错CCl孔216个沉积物样品进行了15种金属元素含量的测试,研究金属元素含量的分布特征,以及与粒度参数的变化关系．结果显示：金属元素的分布特征可分为三组,K、Na、Mg、Al、Ti、Ba、Cu、Zn、Fe、Pb、Cr、V等12种元素具有较为相似的变化趋势;Ca和Sr变化趋势相同;而Mn与其他任何一种元素都不相似．元素分布与粒度参数的相关分析结果表明,Ca、Ti、Pb的变化与沉积物粒度没有明显的关系;K、Na、Al、Ba、Cu、Fe、Cr、V等8种元素与沉积物粘土含量（〈4um）呈正相关关系;Mg、Zn、Mn与粉砂含量（4—63μm）呈正相关关系;而Sr与砂含量（〉63gm）呈正相关关系本研究中大部分元素的粒度效应与其他湖泊、海洋等水体沉积物中元素的粒度效应具有一致的结果．与本岩芯已有的过去1400年来的环境重建资料对比可以发现,在不同的环境变化阶段,元素组合特征都与湖区环境状况具有较好的对应性．其中大部分元素的含量变化受物源条件即流域风化侵蚀程度的影响,而Ca含量不受沉积物粒度变化影响,且与沉积物中碳酸盐含量、Sr／Ba具有很好的相关性,说明其变化受物源条件影响小,而主要与湖水理化性质、蒸发强度以及湖泊沉积过程有关．     

Element Composition and Biogeochemical Functions of Algae Ulothrix Zonata (F. Weber et Mohr) Kützing in the Coastal Zone of the Southern Baikal

ICP-MS method was used to study the element composition of green algae Ulothrix zonata (F. Weber et Mohr) Kützing, sampled in the coastal zone of the Southern Baikal. Dominating in Ulothrix composition are S, Ca, P, Mg and microelements Fe, Al, Ti, Mn, Sr, Ba, Cu, Zn, La, Ce, As, Br, and Pb. The concentrations of all analyzed elements in alga thallomes is greater than the respective concentrations in coastal zone water. The dry mass of U. zonata accumulates more P, As, S, I, Br, Ni, Cd, Ca, and Mg than the stone substrate does. The effect of U. zonata on the formation of element composition of water medium in the coastal zone is demonstrated.     

Dynamics of dissolved major (Na,K, Ca,Mg, and Si) and trace (Al,Fe, Mn,Zn, Cu,and Cr) elements along the lower Orinoco River

This study addresses the changes in dissolved major and trace element concentrations along the Orinoco River, including the mixing zone between the Orinoco and Apure Rivers. Water samples from the Apure and Orinoco Rivers were collected monthly in four sectors over a period of 15 months. Auxiliary parameters (pH, dissolved oxygen, conductivity, and temperature), total suspended sediments, dissolved organic carbon (DOC), and major (Na, K, Ca, Mg, and Si) and trace (Al, Fe, Mn, Zn, Cu, and Cr) element concentrations were measured in all sectors. The relative contribution of both rivers after the Apure–Orinoco confluence was determined using Ca as a tracer. Moreover, a mixing model was developed to determine whether dissolved species exhibit a conservative behavior during mixing. The results indicate that DOC is removed from waters during the Apure–Orinoco mixing, probably due to absorption of DOC on mineral phases supplied by the Apure River. Dissolved Na, Ca, and Mg behave conservatively during the mixing processes, and their concentrations are controlled by a dilution process. The anomaly in the temporal pattern of K in the Orinoco is caused by the input of biogenic K originating from the Apure River during the high‐water stage. The loss of dissolved Si during the low‐water stage can be explained by the uptake of Si by diatoms. Dissolved Mn, Zn, Al, and Fe showed a non‐conservative behavior during the Apure–Orinoco mixing. The removal of Mn and Zn from the dissolved phase can be explained by the formation of Mn‐oxyhydroxides and the scavenging of Zn onto Mn oxides. Dissolved Fe is controlled by redox processes, although the removals of Fe and Al due to the preferential adsorption of large organometallic complexes by mineral surfaces after the Apure–Orinoco confluence can affect the mobility of both elements during transport. The conservative behavior shown by Cu and Cr can be related to the tendency of both elements to be complexed with small organic colloids, which are not preferentially adsorbed by clays.     

Investigations on Mineralogical and Chemical Composition of Suspended Particulate Matter (SPM) in the Odra Estuary

In order to recognize lateral and seasonal variations in composition of suspended particulate matter (SPM) in the Odra Estuary, samples were taken at four sites in the period July 1996 - July 1997 monthly if possible. The contents of the elements Si, Ti, Al, Fe, Mn, Mg, Ca, Na, K, P, C, S as well as Ba, Cr, Sr, V, Zn, Cu, Zr, and of the minerals illite, chlorite, smectite, kaolinite and others have been determined. The decreasing influence of the river Odra towards the open sea could be realized with the help of the contents of the minerals quartz, smectite, and of the elements Ba, Cr, K, P, Si and other. 60% of the seasonal and lateral variations can be explained by changing contents of total carbon (TC), total organic carbon (TOC), Al, Fe, Si, Ti, P, Mn, and Ba. They are mainly caused by differences in the production of organic matter, resuspension, riverine input, and redox-sensitive processes.     

Characteristics of trace elements in aerosols collected in Northern Tunisia

In order to investigate the chemical characteristics of atmospheric aerosols, the sources and variability of atmospheric inputs, aerosols samples were collected during April 2006 and June 2007 in the coastal area of Boumhel, Tunisia. The samples were analysed for thirteen elements including Ca, Fe, Al, Si, Ti, Mg, Mn, K, Na, Cl, S, Zn and Pb using a wavelength dispersive X-ray fluorescence spectrometry. All elements measured in the aerosols of Boumhel revealed differences between the two seasons: the concentrations of all elements were the highest in June and the lowest in April due to the importance of meteorological conditions. The cascade impactor provided mass distributions indicate that Al, Fe, Si, Ti, Na, Cl and S are concentrated in coarse particles. The enrichment factors (EFs) of all elements indicate that Al, Fe, Si, Ca and Ti are mainly derived from soil sources. Na, S and Cl are mostly due to sea salts.     

Cation migration in hydrothermal clays: The problem of mineralization criteria in gas-hydrothermal fluids of hydrothermal fields in Southern Kamchatka

Based on a comprehensive study of the hydrothermal clay layer that occurs in geothermal fields, the conditions of formation of cation composition in argillitized rocks are discussed. Under the influence of gas-water fluids and pore solutions, micro- and nano-mineral mixtures are formed in hydrothermal clays; these mixtures include crystalline, amorphous, and transitional mineral phases. A considerable role in their composition belongs to cations of several metals (Fe, Al, Ti, Na, Mg, Ca, K, Mn, and Ba), as well as Si, C, N, S, and volatiles (F^? and Cl^?). The sources of cations and other elements are unaltered host rocks, newly formed hydrothermal-metasomatic rocks, hydrothermal clays, salt deposits, siliceous, carbonate, and other sediments, as well as deep fluids. In the structures of geothermal anomalies and deposits the ??hydrothermal metasomatic rock??gas-water fluid??newly formed mineral chemical compounds?? united system is formed. Each of the elements of this system takes part in the transportation, accumulation, and redistribution of metals. This approach to studies of the geochemistry of present-day geothermal systems may serve as a foundation for developing criteria for the presence of mineralization in metasomatites, gas-hydrothermal fluids, and new mineral associations.     

Iron oxidation state in lower mantle mineral assemblages: I. Empirical relations derived from high-pressure experiments

The oxidation state of iron can significantly influence the physical and chemical properties of lower mantle minerals. To improve methods for estimation of Fe³⁺/∑Fe, synthetic assemblages of (Mg,Fe)(Si,Al)O₃ perovskite and (Mg,Fe)O ferropericlase were synthesised from oxide starting mixtures in Re or Fe capsules at 26 GPa and 1650-1850 °C using a multianvil press. (Mg,Fe)(Si,Al)O₃ majorite was also present in some of the run products. Both electron energy loss spectra (EELS) and Mössbauer spectra were measured for each run product, and a robust fitting method was developed for Mössbauer spectra using EELS results as a standard that enabled Fe³⁺/∑Fe of (Mg,Fe)(Si,Al)O₃ perovskite to be determined from Mössbauer spectra of multiphase assemblages. There is a close to linear variation between Fe³⁺/∑Fe and Al concentration in (Mg,Fe)(Si,Al)O₃ perovskite, independent of oxygen fugacity. The concentration of Fe³⁺ in (Mg,Fe)O increases with increasing iron concentration along curves of constant oxygen fugacity, where higher oxygen fugacity stabilises greater Fe³⁺ concentrations. Fe²⁺/Mg partition coefficients calculated from chemical composition data corrected for measured Fe³⁺/∑Fe showed values nearly identical within experimental error for all samples, and independent of Al concentration and oxygen fugacity. Simple empirical relations were derived to calculate Fe³⁺/∑Fe in (Mg,Fe)(Si,Al)O₃ perovskite and (Mg,Fe)O ferropericlase samples for which no Mössbauer or EELS data were available, and tested by applying them to calculation of Fe²⁺/Mg partition coefficients from literature data for (Mg,Fe)(Si,Al)O₃ perovskite-(Mg,Fe)O assemblages where only total iron concentrations had been measured. Results showed Fe²⁺/Mg partition coefficients that were equal to existing values within experimental error, hence confirming the validity of the empirical relations.     

Element geochemistry and cleaning potential of the No. 11 coal seam from Antaibao mining district

It has aroused great attention that the mobilization of potential toxic substance during coal mining, pro- cessing and using has serious negative influence on environment. Clearly, the coal cleaning can be prop-erly applied to removing hazardous elements or re-ducing their concentrations prior to combustion, which also is considered as an economical and effective technique in minimizing some of these problems[1]. Unfortunately, there are fairly few studies on the parti-tioning behavior of trac…     

The Precipitation Chemistry over Central Bohemia: Attempt to Estimate the Sources and Pathways

An attempt to indicate the sources and pathways of selected chemical substances in precipitation over central Bohemia was accomplished with help of bulk samples, collected in a forested rural landscape approx. 30 km SE from Prague, capital of the Czech Republic. Samples have been collected monthly throughout the 1990s. They were analyzed to determine the concentration of selected major cations and anions (Na⁺, K⁺, Ca²⁺, Mg²⁺, NH₄ ⁺, SO₄ ^2-, NO₃ ^-, Cl^-), as well as several minor and trace elements (Al, As, Be, Cd, Cu, Fe, Mn, Pb, Sr, Zn, F^-).Set of the bulk samples shows strong mutual correlation of the main acidifiers - compounds of N, S (and F). Good correlation occurs also at the typical lithogenic elements Al, K, Na, Ca, Mg, Sr, and the typical elements originating from the flue gases of the combustion chambers burning low quality brown coal - As, (Be), Cd, Cu, Pb, and Zn. The only strong correlation of Cl with Na (and Mg) indicates that majority of these elements originates from the oceanic spray. The content of pollutants in precipitation depends on the air masses types and on the rout of their approach to the sampling site. The typing of synoptic situations was employed for the determination of the air masses types and routs and of the corresponding fronts and precipitation fields.     

Investigation of Chemical Compositions of Urban,Industrial, Agricultural,and Rural Top‐soils in Izmir,Turkey

The top‐soil samples were collected from urban, industrial, agricultural, and rural sites to investigate the modification in the elemental composition due to anthropogenic influence in one of the biggest city of Turkey, namely Izmir. The elemental profiles were dominated by lithophilic elements such as Al, Ca, Fe, Mg, K, and sea salt element, Na, which is typical for Mediterranean region. The trace elemental concentrations showed significant variation with higher concentrations in the industrial sites, particularly in the vicinity of iron‐steel producers from scrap materials (EAF‐Steels). Lead, Zn, and Cd around EAF‐Steels were found to be higher than other sites. Comparison to universal upper crusts and local reference soil has shown that Izmir top‐soils were contaminated in terms of many trace elements, most probably due to anthropogenic activities. Correlation matrix, crustal enrichment factors, and factor analysis were applied to investigate the extent of soil modification and possible sources. The results indicated that the elemental profiles of top‐soils were mainly determined by parent materials; however, anthropogenic activities were found to be factor effective on the profile.     

Neutron capture logging calibration and data analysis for environmental contaminant assessment

This paper describes a method to calibrate a neutron capture sonde equipped with a high resolution γ-ray detector, and analyze log data. The method utilizes the 1460.8-keV passive γ-ray of ⁴⁰K, the 770.3-keV capture γ-ray of ³⁹K, and a capture γ-ray from a target element. An equation containing the spectral line intensities for the two capture γ-rays, nuclear capture data, and the detector efficiency function expresses the concentration of the target element as a multiple of the ³⁹K concentration. The concentration of ³⁹K is easily deduced from the ⁴⁰K concentration, which is calculated directly from the line intensity for the 1460.8-keV γ-ray in a passive γ-ray spectrum.The calibration automatically adjusts to changes in the neutron transport properties of the logged medium that may result, for example, from variations in the H density and the concentrations of neutron poisons. Fluctuations in the neutron source output are similarly accommodated. The calibration utilizes U.S. Department of Energy (DOE) passive γ-ray calibration standards that contain well established concentrations of K, U, and Th. The passive γ-rays from K, U, and Th (and the U and Th decay progenies) provide data for the detector efficiency function determination.Data for proof-of-principle demonstrations of the method were acquired by logging boreholes penetrating the shallow subsurface at a DOE waste site with a simple, reliable neutron capture logging system. The system had a ²⁵²Cf source and a high purity germanium (HPGe) detector. Time gating could not be used to sort signals originating from capture and activation, but the excellent energy resolution permitted capture γ-ray identifications based solely on the γ-ray energies. Cl, H, and other elements were detected and assessed.A conventional calibration and data analysis method was also employed. The method was specific to Cl and was based on measurements in two Cl-impregnated concrete blocks. Cl concentrations inferred with this method were often consistent with the concentrations determined with the new method. When the two methods produced different Cl concentrations, the discrepancies could be explained by variations in formation parameters.     

Evaluation of metal contamination in coastal sediments of the Bay of Bengal, India: geochemical and statistical approaches

Surface sediment samples collected from the inner shelf region of the Bay of Bengal, were analysed for the major elements and total and acetic acid available trace elements (Al, Ca, Cd, Co, Cr, Cu, Fe, K, Mg, Mn, Na, Ni, P, Pb, Si, Zn) to evaluate geochemical processes influencing their distribution. Major elemental analysis showed that the sediments had high concentrations of Si and relatively low concentrations of Al and Fe. Both major elemental and trace metal concentrations indicated that the sediments represent weathered products of granite and charnockite. Normalization of metals to Al indicated relatively high enrichment factors for Pb, Cd, Zn and Cr. The higher proportions of nondetrital Pb (66%), Cd (41%) and Co (28%) reveal metal contamination due to anthropogenic inputs. Factor analysis (FA) identified six possible types of sedimentological and geochemical associations. The dominant factor accounting for 26.9% of the total variance identifies an anthropogenic input and accumulation of nondetrital Cd, Co, Cr, Ni and Pb. Association of these metals with CaCO3 reveals that shell fragments in the surface sediments are likely act as a carrier phase for nondetrital metals. The results are discussed in the context of the sources and pathways of elements in the Bay of Bengal.     

Temporal variability of selected dissolved elements in the lower Orinoco River,Venezuela

Monthly analyses of pH, conductance, alkalinity, total suspended solids, dissolved major cations (Na, K, Ca and Mg), and selected dissolved trace elements (Fe, Al, Mn, Cu, Zn and Cr) were conducted on waters of the lower Orinoco River from February 2004 to May 2006. The data show strong seasonal variability. Major cations had maximum concentrations at low water, and were correlated with pH, conductance and alkalinity because of the tributaries coming from the Andean zones, where the weathering of evaporites and carbonate shales controls water chemistry. K concentrations did not show any relation with evaporite weathering, probably because large amounts of K come from the Guayana Shield rivers as a consequence of feldspar weathering. The concentrations of dissolved Fe, Mn and Cu were highest during the high water stage. Concentrations of the elements K, Cr, Zn and Cu are correlated with each other but not with dissolved Fe and Al, which probably are complexed with humic and fulvic substances. Mn concentrations did not show relationships with other variables. Inter‐annual variability of dissolved elements is explained by temporal changes in precipitation. Copyright © 2008 John Wiley & Sons, Ltd.     

气温气压与断层气氡浓度短期变化的相关性分析

以嘉峪关断层气氡为研究对象, 利用气氡和气温、 气压的日值, 通过计算气温气压与气氡浓度的相关系数, 分析了气温和气压对断层气氡浓度短期变化的影响. 结果显示, 气温和气压对气氡浓度的短期影响显著, 其表现为既具有相似性特征, 又存在明显的差别: ① 在对气氡浓度的影响程度上, 气压明显大于气温. ② 气温和气压对气氡浓度的影响均具有明显的滞后效应, 如离取样时间最近的0—8时, 它们对气氡浓度的影响均逐渐减弱, 但气温对气氡浓度的影响于7时达到最低, 8时仍在低位变化; 而气压对气氡浓度的影响则在8时达到最低值. 9时气温和气压的影响都出现快速上升, 之后气压对气氡浓度的影响表现为波动缓慢上升变化, 18—19时达到最高值; 9时之后气温对气氡浓度的影响则表现为波动缓慢下降变化. ③ 不同月份气压和气温对气氡浓度的影响也存在明显的差异. 气压的影响具有很好的规律性, 1—4月为高影响状态, 5月份开始出现快速下降变化, 8月份达到最低值, 9月份略有回返, 10—12月又达到了全年的最高值; 而气温对气氡浓度的影响除3月份和4月份比较高之外, 其它月份都在低值变化, 并且差别不大. ④ 对震例的分析结果表明, 嘉峪关气氡浓度大幅正突跳变化不具备预报地震的能力.      

Accumulation of alkaline and alkaline-earth elements in subcolloidal fraction of bottom sediment at the river-sea geochemical barrier

Data on the concentrations of alkaline (K, Li, Cs, Rb, Tl), alkaline-earth (Mg, Be), and other elements and humic acids in subcolloidal fraction of bottom sediment at river-sea geochemical barrier are given. Higher concentrations of Al and Mg is detected in river BS corresponding to the initial stage of water mixing. The increase in the concentrations of Li, Cs, and Rb is shown to best correspond to the accumulation of humic acids in marine deposits.     

Temporal and spatial variations in the geochemistry of major and minor particulate and selected dissolved elements of Thermaikos Gulf, Northwestern Aegean Sea

The objectives of this study were to examine both spatial and temporal changes of particulate major elements and minor metals, as well as dissolved Mn and Cd, in the waters of Thermaikos Gulf. Collections of water and suspended particulate matter (SPM), as depth profiles (5–8 depths), were undertaken at 10 principal stations, essentially on a N–S traverse of the western side of the Gulf.One of the principal aims of the study was to observe if there was any change in the patterning of the elements between the three occupations of the stations: (a) in September 2001, immediately before the commencement of trawling; (b) in October 2001, whilst fishing was active; and (c) in winter/early spring conditions (February 2002), when fishing was still active, but after a change of river/atmospheric conditions.Bottom (20 m) waters were dominated by sediment resuspension; this was identified by concentration changes in the aluminosilicate elements (e.g. Al, Ti, K, Fe) of the SPM. A two- to three-fold increase occurred between September and October, caused probably by trawling; this was sustained at the offshore stations, in February. During February, the western inshore stations showed little sediment resuspension, caused by extreme winter cooling and the sinking of water. Consequently, a N–S density discontinuity existed at all water depths, which prevented the thermohaline cyclonic circulation from penetrating into the western seaboard of the Gulf. The distribution of dissolved and particulate Mn in the lower waters was due to redox cycling of the element at the benthic boundary; this was more intense in the north, where the organic supply was higher.Biogenic element concentrations and Ca/Al, Si/Al ratios showed no evidence that trawling activity promoted higher biological production. Strong correlations of Co, Cr, Ni and V, with Al and K, showed that these elements were associated strongly with detrital aluminosilicates. However, the variable association of Cd, Pb and Zn, with K (and Al), especially in the upper waters, implied an anthropogenic source derived from the rivers and the city of Thessaloniki. Examination of the Kd's of Cd showed a two-order of magnitude decrease with depth, caused by resuspension and possible advection of relatively unpolluted sediments, into the western Gulf.     

The volcanic acidification of glacial Lake Caviahue,Province of Neuquen,Argentina

Lake Caviahue (northern Patagonia, Argentina) is a large glacial lake acidified by volcanic fluids from Copahue volcano. The lake and the feeding rivers were sampled annually from 1997 till early 2006, including the eruptive period of 2000. Lake Caviahue waters evolved over time, with the most concentrated waters in 2000 during the eruptive period, followed by gradual dilution that was interrupted by renewed acidification in 2003–2004. Inversion of the lake water data and application of a dynamic non-steady state model for the lake provides our best quantitative estimates for the variation in element fluxes over the 9-year period. The model flux results agree well with most of the measured fluxes. The Copahue hydrothermal system had gently declining element fluxes between 1997 and mid-1999, although the lake was still becoming more concentrated. About 2–3 months before the 2000 eruption, element fluxes increased strongly, but the hydrothermal fluxes almost shutoff directly after the main eruptive events. The fluxes of several elements recovered post-2001, with an increase in element fluxes in 2003–2004; the lake became more dilute between 2004 and 2006. The intrusion of new magma into the hydrothermal system just prior to the 2000 eruption led to enhanced water rock interaction, with higher concentrations of the rock forming elements in the fluids, and the hot spring flow rate increased as a result of the higher pressure in the reservoir. The fluids became saturated in alunite and jarosite, and they were already saturated with anhydrite. Precipitation of these minerals possibly led to a decreased permeability of the hydrothermal reservoir, leading to the strongly reduced element fluxes just after the eruption. In addition, K, Al and S were retained in the newly precipitated minerals as well, further diminishing their export. The acidification in 2003–2004 may have resulted from a new small intrusion of magma or resulted from seismic activity that created new permeability and fresh rock surfaces for water rock interaction. The volcano is a significant source of toxic trace elements such as F, As, B and Li as well as a nutrient (P) for the local watershed. Monitoring of the hydrothermal fluids in the river that drains Copahue, especially the S/Cl, Mg/Cl and Mg/K values as well as the magnitude of the element fluxes would provide the best information for eruption forecasting for this volcano.     

Biogeochemistry of dissolved carbon,major, and trace elements during spring flood periods on the Ob River

Detailed knowledge of the flood period of Arctic rivers remains one of the few factors impeding rigorous prediction of the effect of climate change on carbon and related element fluxes from the land to the Arctic Ocean. In order to test the temporal and spatial variability of element concentration in the Ob River (western Siberia) water during flood period and to quantify the contribution of spring flood period to the annual element export, we sampled the main channel year round in 2014–2017 for dissolved C, major, and trace element concentrations. We revealed high stability (approximately ≤10% relative variation) of dissolved C, major, and trace element concentrations in the Ob River during spring flood period over a 1‐km section of the river channel and over 3 days continuous monitoring (3‐hr frequency). We identified two groups of elements with contrasting relationship to discharge: (a) DIC and soluble elements (Cl, SO₄, Li, B, Na, Mg, Ca, P, V, Cr, Mn, As, Rb, Sr, Mo, Ba, W, and U) negatively correlated (p < 0.05) with discharge and exhibited minimal concentrations during spring flood and autumn high flow and (b) DOC and particle‐reactive elements (Al, Fe, Ti, Y, Zr, Nb, Cs, REEs, Hf, Tl, Pb, and Th), some nutrients (K), and metalloids (Ge, Sb, and Te), positively correlated (p < 0.05) with discharge and showed the highest concentrations during spring flood. We attribute the decreased concentration of soluble elements with discharge to dilution by groundwater feeding and increased concentration of DOC and particle‐reactive metals with discharge to leaching from surface soil, plant litter, and suspended particles. Overall, the present study provides first‐order assessment of fluxes of major and trace elements in the middle course of the Ob River, reveals their high temporal and spatial stability, and characterizes the mechanism of river water chemical composition acquisition.     

镍添加对水鳖(Hydrocharis dubia)叶片镍和营养元素含量以及氧化胁迫和抗氧化系统的影响

采用营养液水培的方法,研究不同镍(Ni)添加浓度(0、0.05、0.10、0.15、0.20 mmol/L)对水鳖(Hydrocharis dubia)叶片中Ni元素积累、营养元素(Ca、Mg、K、Fe和Mn)含量、氧化胁迫和抗氧化系统的影响.结果显示:(1)叶片中Ni含量以浓度依赖的方式增加;(2)叶片中营养元素含量(Ca、Mg、K、Fe、Mn)也受影响,其中Ca、Mg含量随Ni浓度增加而显著上升;K含量随Ni浓度增加有所升高,但不显著;Mn含量虽在较大Ni浓度时有所下降,但处理组始终高于对照组;而Fe含量则随Ni浓度增加而下降;(3)Ni胁迫诱导了明显的氧化胁迫,主要表现为:O·-2产生速率以及过氧化氢和丙二醛含量显著升高,可溶性蛋白以及光合色素含量明显下降;(4)随着Ni浓度的升高,过氧化物酶活性逐渐升高,过氧化氢酶活性呈下降趋势,超氧化物歧化酶活性在Ni添加浓度为0.05 mmol/L时出现短暂升高随后下降;维生素E和黄酮含量随Ni浓度增加呈缓慢上升趋势;还原型谷胱甘肽未发生明显变化,非蛋白巯基和植物络合素含量均表现为先升后降的趋势;总抗氧化能力随Ni浓度升高先增强后减弱.由此可见,Ni添加引起水鳖叶片中Ni元素的累积和营养元素含量变化,同时产生明显的氧化胁迫,打破了抗氧化系统的平衡.