广州市酸雨成分及其相关分析

分析了2003年11月-2004年10月广州市龙洞79次降雨的化学组分及其各组分之间的相关关系。得出:(1)观测期间总降雨量1359.8,单次降雨的pH值在3.22-7.29之间,平均4.83;以pH<5.6为酸雨的临界值,则酸雨频率占降雨次数的77.2%或占降雨量的81.5%;(2)广州降水的化学组成以SO₄^2-、Cl^-和NO₃^-为主要阴离子,阳离子中以Ca²⁺、NH₄⁺、Na⁺所占比例较大;(3)广州地区酸雨属硫酸型,降雨中的SO₄^2-、NO₃^-、PO₄^3-、Cl^-、NH₄⁺、K⁺、Na⁺、Ca²⁺、Mg²⁺离子浓度分别为0.150,0.045,0.002,0.163,0.058,0.006,0.013,0.083和0.007mol·L^-1,单次降雨的SO₄^2-/NO₃^-比值在0.42-17.6之间,年平均为3.33,该值比西南地区相应值低许多,而且与同一地点5年前测定的结果相比较,SO₄^2-/NO₃^-比值有变小的趋势,说明广州地区NO_x排放量高逐渐增加;(4)广州地区酸雨有着明显的季节变化规律,春、夏、秋季酸雨比较严重,冬季酸雨较少出现,这与西南地区的重庆(冬季酸雨较春季严重)酸雨季节规律相反;(5)通过SPSS统计分析得出,雨量与各化学组分含量成负相关,说明雨量对大气污染物质的稀释作用;酸雨各化学成分之间存在着一定的相关性,如SO₄^2-与Ca²⁺,NO₃^-与NH₄⁺,K⁺与Na⁺、Mg²⁺离子,Na⁺与Mg²⁺等都存在显著的正相关,利用这种相关可以建立某些酸雨成分的预测模型。     

盐胁迫下外源褪黑素和Ca2+对甜瓜幼苗的缓解效应

以甜瓜品种‘羊角酥瓜’为试材,利用人工气候室控制环境条件(昼/夜25/18 ℃),研究盐胁迫条件下外源褪黑素(MT)和Ca²⁺对甜瓜幼苗根系和叶片中Cl^-、Na⁺、K⁺、Mg²⁺、Ca²⁺离子含量,Na⁺/K⁺、 Na⁺/Ca²⁺、Na⁺/Mg²⁺值,以及H⁺-ATP酶活性、渗透调节物质积累和细胞膜质过氧化的影响.结果表明: 与对照相比,盐胁迫处理显著抑制甜瓜幼苗生长,增加根系和叶片中Cl^-、Na⁺含量,降低K⁺、Mg²⁺、Ca²⁺含量.盐胁迫下,喷施外源MT或Ca²⁺处理均可以显著降低甜瓜根系和叶片中Cl^-、Na⁺含量,提高K⁺、Mg²⁺、Ca²⁺含量,植株体内Na⁺/K⁺、Na⁺/Ca²⁺和 Na⁺/Mg²⁺值下降;同时也提高了根系和叶片H⁺-ATP酶活性及叶片渗透调节物质的含量,降低盐胁迫对细胞膜的伤害,表现在甜瓜叶片相对电导率和丙二醛含量降低.总之,在盐胁迫条件下,外源MT、Ca²⁺单独和复配处理均可通过提高H⁺-ATP酶活性来降低盐害离子的含量,改善甜瓜幼苗中的离子平衡,同时增加渗透调节物质的含量,降低膜质过氧化水平,从而增强其对盐胁迫的适应性,其中MT和Ca²⁺复配处理时的效果更好.复配外施 MT 和Ca²⁺在诱导甜瓜幼苗提高耐盐方面具有协同增效作用.     

盐胁迫下外源褪黑素和Ca2+对甜瓜幼苗的缓解效应

以甜瓜品种‘羊角酥瓜’为试材,利用人工气候室控制环境条件(昼/夜25/18 ℃),研究盐胁迫条件下外源褪黑素(MT)和Ca²⁺对甜瓜幼苗根系和叶片中Cl^-、Na⁺、K⁺、Mg²⁺、Ca²⁺离子含量,Na⁺/K⁺、 Na⁺/Ca²⁺、Na⁺/Mg²⁺值,以及H⁺-ATP酶活性、渗透调节物质积累和细胞膜质过氧化的影响.结果表明: 与对照相比,盐胁迫处理显著抑制甜瓜幼苗生长,增加根系和叶片中Cl^-、Na⁺含量,降低K⁺、Mg²⁺、Ca²⁺含量.盐胁迫下,喷施外源MT或Ca²⁺处理均可以显著降低甜瓜根系和叶片中Cl^-、Na⁺含量,提高K⁺、Mg²⁺、Ca²⁺含量,植株体内Na⁺/K⁺、Na⁺/Ca²⁺和 Na⁺/Mg²⁺值下降;同时也提高了根系和叶片H⁺-ATP酶活性及叶片渗透调节物质的含量,降低盐胁迫对细胞膜的伤害,表现在甜瓜叶片相对电导率和丙二醛含量降低.总之,在盐胁迫条件下,外源MT、Ca²⁺单独和复配处理均可通过提高H⁺-ATP酶活性来降低盐害离子的含量,改善甜瓜幼苗中的离子平衡,同时增加渗透调节物质的含量,降低膜质过氧化水平,从而增强其对盐胁迫的适应性,其中MT和Ca²⁺复配处理时的效果更好.复配外施 MT 和Ca²⁺在诱导甜瓜幼苗提高耐盐方面具有协同增效作用.     

磷饥饿对番茄幼苗H+分泌及Pi吸收的影响

磷饥饿条件下番茄幼苗的H⁺分泌速率明显提高。质膜质子泵专一性抑制剂钒酸盐能显著抑制番茄幼苗的H⁺分泌,也能显著抑制其Pi吸收。此结果表明,磷饥饿时番茄幼苗Pi吸收速率的变化与H⁺分泌速率的变化之间可能具有一定的相关性,并进一步暗示质膜H⁺-ATPase可能参与其中。本文结果还表明,Pi/H⁺的准量关系约为1:1。     

外源γ-氨基丁酸调控甜瓜叶绿体活性氧代谢应对短期盐碱胁迫

以甜瓜品种‘金辉1号’为试材,采用深液流水培法,研究外源γ 氨基丁酸(GABA)对短期盐碱胁迫下甜瓜幼苗叶绿体活性氧代谢的调控作用.结果表明: 盐碱胁迫显著提高了甜瓜叶绿体内光合色素、丙二醛(MDA)和过氧化氢(H₂O₂)含量及超氧阴离子(O^-_·2)产生速率;增加抗坏血酸(AsA)和谷胱甘肽(GSH)等抗氧化物质含量;明显抑制H⁺-ATP酶(H⁺-ATPase)和H⁺ 焦磷酸酶(H⁺-PPiase)活性.外源叶面喷施GABA有效抑制了盐碱胁迫引起的叶绿体内O^-_·2、H₂O₂和MDA的积累,缓解了光合色素增加的趋势;显著提高SOD和AsA GSH循环各个酶的活性,增加了AsA和GSH库,降低了AsA/DHA和GSH/GSSH比值,增强了H⁺-ATPase和H⁺-PPiase 活性.表明外源GABA能加快叶绿体内活性氧代谢,促进AsA-GSH循环的运转,维持细胞膜的渗透性,进而缓解了盐碱胁迫引起的氧化伤害.     

硅对镉胁迫下香椿幼苗光合特性和离子吸收的影响

为探究硅对镉胁迫下香椿的缓解机制,以香椿幼苗为材料,采用水培法调查施加不同浓度硅(0、0.5、1.0和2.0 mmol·L^-1)对镉(200μmol·L^-1)胁迫下香椿幼苗的生长指标、渗透平衡、离子吸收、光合特性、抗氧化能力的影响。结果表明：镉胁迫显著抑制香椿幼苗的生长,降低其根系活力、离子含量、光合色素含量、净光合速率(P_n)、气孔导度(G_s)、蒸腾速率(T_r);而相对电导率、胞间CO₂浓度(C_i)、过氧化氢(H₂O₂)和丙二醛(MDA)含量则显著增加。与单独镉处理相比,施加硅后,香椿幼苗的生长指标、根系活力、铁(Fe²⁺)、锰(Mn²⁺)、锌(Zn²⁺)、铜(Cu²⁺)离子含量、叶绿素和类胡萝卜素含量以及气体交换参数(除C_i)均显著提高,而镉离子(Cd²⁺)...     

松嫩平原盐碱土饱和浸提液与土水比1:5浸提液间化学参数的换算关系

采用饱和浸提液与土水比1:5浸提液两种方法分析了松嫩平原94份盐碱土样品的电导率、钠吸附比、主要阳离子(Na+、K+、Ca2+、Mg2+)以及总阳离子浓度等化学参数,并对两种方法测定的盐碱化参数相关性进行了研究.结果表明:饱和浸提液电导率、钠吸附比、总阳离子浓度、Na+离子浓度与土水比1:5浸提液相应参数存在极显著的相关关系,其关系方程可用于松嫩平原盐碱土饱和浸提液与1:5浸提液间化学参数的换算;而K+、Ca2+、Mg2+离子浓度在两种浸提液间不存在相关性.     

不同生境下胡杨树体离子平衡及其与土壤因子关系

为探讨胡杨适应盐渍环境的离子分布规律,揭示胡杨的耐盐生理机制,以高盐和低盐两种不同生境中的胡杨(Populus euphratica)为对象,测定其根、树干、老枝、幼枝、叶片等不同器官中Na⁺、K⁺、Ca²⁺、Cl^-的含量,并分析各离子吸收、运输和分配特征的差异及其与土壤因子的关系。结果表明：(1)胡杨叶片中Na⁺、Cl^-含量在高盐生境下显著低于低盐生境,K⁺含量在高盐生境下显著高于低盐生境,其他器官的各离子含量变化均不显著;胡杨老枝、幼枝、叶片的K⁺/Na⁺在高盐生境下均显著高于低盐环境、Ca²⁺/Na⁺增幅不明显;在高盐生境下,根系选择吸收K⁺能力显著低于低盐环境,但吸收Ca²⁺能力较强,且各器官对Ca²⁺、K⁺选择向上运输的能力更强。(2)在低盐环境中Na...     

罗布麻对不同浓度盐胁迫的生理响应

利用网室盆栽实验, 研究不同浓度的NaCl(100–400 mmol·L^–1)胁迫对罗布麻(Apocynum venetum)生长及生理特性 的影响。结果表明, 100 mmol·L^–1NaCl处理显著降低了罗布麻植株的鲜重, 但对其干重影响不大; 随着盐浓度继续增加, 罗布麻鲜重和干重显著下降。在盐胁迫下, 罗布麻叶片内的丙二醛含量、电解质渗漏率、根部和地上部Na⁺的含量明显增加, K⁺的含量随着盐离子浓度的增加而降低。盐胁迫显著降低了地上部Ca²⁺的含量, 而对根部Ca²⁺的含量没有影响。植株K⁺/Na⁺和Ca²⁺/Na⁺比值随着盐胁迫强度的增加而降低。盐胁迫显著促进了罗布麻根部对K⁺和Ca²⁺的选择性吸收及对K⁺的选择性运输。当NaCl浓度小于或等于200 mmol·L^–1时, 随着盐离子浓度的增加, 罗布麻叶片内的脯氨酸和可溶性糖积累显著增加,而当NaCl浓度大于200 mmol·L^–1时, 这2种有机溶质含量显著下降。总体上, 罗布麻通过积累无机离子、合成有机溶质及维持较高的K⁺、Ca²⁺选择性吸收和运输来适应一定浓度(≤200 mmol·L^–1NaCl)的盐胁迫。     

再力花处理河涌和湖泊水样有机污染物及离子的特性

为了明确河涌和湖泊水样中COD、TP、TN和阴阳离子的植物处理效果,以及含氮污染物的植物转化规律,以前期研究中选育的再力花处理了广州市某河涌和暨南大学明湖水样.结果证明,再力花能有效地促进河涌和湖泊水样中TN、COD_Cr和TP的去除.处理144h后,河涌水样初始浓度为11.15mg·L^-1、45mg·L^-1和1.17mg·L^-1的TN、COD_Cr和TP分别降至3.21mg·L^-1、15.8mg·L^-1和0.53mg·L^-1;湖水初始浓度为4.50mg·L^-1、36mg·L^-1和0.25mg·L^-1的TN、COD_Cr和TP分别降至2.31mg·L^-1、11.7mg·L^-1和0.03mg·L^-1.水样中的微生物和再力花均能去除NH₄⁺,并引起水中还原态氮发生亚硝化和硝化,但是不会明显改变Cl^-、SO₄^2-、Na⁺、K⁺、Mg²⁺和Ca²⁺等离子的浓度.     

The mechanism of hydrolysis of beta-glycerophosphate by kidney alkaline phosphatase.

1. To identify the functional groups that are involved in the conversion of beta-glycerophosphate by alkaline phosphatase (EC 3.1.3.1) from pig kidney, the kinetics of alkaline phosphatase were investigated in the pH range 6.6-10.3 at substrate concentrations of 3 muM-30 mM. From the plots of log VH+ against pH and log VH+/KH+m against pH one functional group with pK = 7.0 and two functional groups with pK = 9.1 were identified. These groups are involved in substrate binding. Another group with pK = 8.8 was found, which in its unprotonated form catalyses substrate conversion. 2. GSH inhibits the alkaline phosphatase reversibly and non-competitively by attacking the bound Zn(II). 3. The influence of the H+ concentration on the activation by Mg2+ ions of alkaline pig kidney phosphate was investigated between pH 8.4 and 10.0. The binding of substrate and activating Mg2+ ions occurs independently at all pH values between 8.4 and 10.0. The activation mechanism is not affected by the H+ concentration. The Mg2+ ions are bound by a functional group with a pK of 10.15. 4. A scheme is proposed for the reaction between enzyme, substrate, Mg2+ and H+ and the overall rate equation is derived. 5. The mechanism of substrate binding and splitting by the functional groups of the active centre is discussed on the basis of a model. Mg2+ seems to play a role as an autosteric effector.     

Effect of pH, ionic strength and univalent inorganic ions on the reconstitution of aspartate aminotransferase

1. The effect of pH change on the reconstitution of aspartate aminotransferase (EC 2.6.1.1), i.e. the reactivation of the apoenzyme with coenzyme (pyridoxal phosphate and pyridoxamine phosphate), was studied in the pH range 4.2-8.9 by using three buffer systems at concentrations ranging from 0.025 to 0.1m. 2. Although the profile of the reconstitution rate-pH curve in the range pH5.2-6.8 (covered by sodium cacodylate-HCl buffer) reflects the influence of the H(+) concentration on the reconstitution process, the profile of the curve in the pH ranges 4.2-5.6 and 7.2-8.25 (covered respectively by sodium acetate-acetic acid and Tris-HCl buffers) appears to be influenced by the ionic strength of the buffer. 3. The reconstitution is also influenced by univalent inorganic ions such as halide ions and, to a lesser extent, alkali metal ions, which are known to alter the water structure.     

Stimulation of valyl- and isoleucyl-tRNA synthetase reactions by polyamines

The aminoacylation of tRNA catalysed by valyl-tRNA synthetase (EC 6.1.1.9) and isoleucyl-tRNA synthetase (EC 6.1.1.5) fromMycobacterium smegmatis is dependent on the presence of divalent metal ions. Polyamines alone, in the absence of metal ions, do not bring about aminoacylation. In the presence of suboptimal concentrations of Mg²⁺, polyamines significantly stimulate the reaction. Of the cations tested, only Mn²⁺, Co²⁺ and Ca²⁺ can partially substitute for Mg²⁺ in aminoacylation, and spermine stimulates aminoacylation in the presence of these cations also. At neutral pH, spermine deacylates nonenzymatically aminoacyl tRNA. AMP and pyrophosphate-dependent enzymatic deacylation of aminoacyl-tRNA (reverse reaction) is also stimulated by spermine. The inhibitory effect of high concentration of KC1 on aminoacylation is counteracted, by spermine. The low level of activity between pH 8.5–9.0 at 1.2 mM Mg²⁺ is restored to normal level on the addition of spermine. The inhibitory effect of high pH on aminoacylation in the presence of low concentration of Mg²⁺ is also prevntedvby spemine.     

Solubility and mobility of copper,zinc and lead in acidic environments

Understanding the chemical speciation of metals in solution is necessary for evaluating their toxicity and mobility in soils. Soil samples from the Powder River Basin, Wyoming were extracted with distilled deionised H₂O. Soil water extracts were subjected to chemical speciation to determine the relative distribution and chemical forms of copper (Cu), zinc (Zn) and lead (Pb) in acidic environments. As pyrite oxidised, the pH decreased from 6.6 to 2.4, concentration of dissolved sulfate (S_T) increased from 259 to 4,388 mg L^-1 and concentration of dissolved organic carbon (DOC) decreased from 56.9 to 14.4 mg L^-1. Dissolved Cu concentrations ranged from 0.06 to 0.42 mg L^-1 and dissolved Zn concentrations ranged from 0.084 to 4.60 mg L^-1. Dissolved concentrations of Pb were found to be 0.003 to 0.046 mg L^-1. Chemical speciation indicated that at near neutral pH, dissolved metal concentration in soil water extracts was dominated by DOC- metal complexes. At low pH, dissolved metal concentration in soil water extracts was dominated by free ionic forms (e.g. Cu²⁺, Zn²⁺, Pb²⁺) followed by ion pairs (e.g. CuSO₄ ⁰, ZnSO _inf4 ^sup0 , PbSO _in4 ^sup0 ). Results obtained in this study suggest that as soil pH decreased, the availability and mobility of metal ions increased due to the chemical form in which these metal ions are present in soil solutions.     

Determination of free Ca ion concentrations with an ion-selective electrode in the presence of chelating agents in comparison with calculated values.

Experimentally determined free Ca ion concentrations, measured with a Ca-selective electrode, were compared with values calculated with a computer program utilizing stability constants of the chelating agents: NTA, EDTA, and EGTA used to set the free ion concentration in the range of 10^?3 to 10^?6m. In the presence of 0.1 m KCl, 2 mm MgCl₂, 20 mm Hepes (pH 7.4), 2 mm ATP, 0.1 mm CaCl₂ (total concentration), and various ligand concentrations the measured free Ca²⁺ levels were found to be approximately six to seven times greater than the computer-derived values. Apparent stability constants for Ca-ATP, Ca-EDTA, and Ca-EGTA were determined under these experimental conditions.     

不同耐盐植物根际土壤盐分的动态变化

以甘肃秦王川引大灌区盐渍化土壤为研究背景,用盆栽根袋法对4种耐盐植物根际和非根际土壤pH和盐分离子的动态变化进行了分析比较。结果表明:4种待测植物随着培养时间的延长土壤pH和EC值呈降低趋势。新疆大叶(Medicago Sativa L.cv.Xinjiangdaye)、向日葵(Helianthus annuus)和霸王(Zygophyllum xanthoxylum)生长90 d后根际土壤pH明显低于非根际,而裸麦(Hordeum vulgare var. vulgare)根际较非根际pH差异不大。霸王和新疆大叶根际土壤EC值较非根际高,而裸麦和向日葵的根际与非根际差异不大。4种供试植物根际K⁺均出现亏缺,Ca²⁺、Na⁺、Mg²⁺、SO^2-₄和Cl^-在新疆大叶、霸王和向日葵3种植物根际均出现富集,对于裸麦:Ca²⁺、Mg²⁺和SO^2-₄ 3种离子在植物根际富集,而Cl^-和Na⁺在根际亏缺。随着待测植物培养时间的增加Na⁺/K⁺、Na⁺/Ca²⁺和Na⁺/Mg²⁺ 这3个比值呈降低趋势,说明Na⁺相对于K⁺、Ca²⁺和Mg²⁺的含量降低,生物措施对Na⁺的移除效果较显著。     

Effect of Varying the Ionic Concentration of a Microdialysis Perfusate on Basal Striatal Dopamine Levels in Awake Rats

In vivo microdialysis was used to study the effects of Ca2+, Mg2+, and K+ ion concentrations on basal extracellular (EC) levels of striatal DA and metabolites in awake rats on the second day (48 h) after implantation of a microdialysis probe. Basal EC striatal dopamine (DA) levels were markedly (90%) and reversibly reduced by removal and subsequent replacement of Ca2+ ions from the microdialysis perfusate. This implies that the EC DA in this preparation is primarily of synaptic origin. The addition and subsequent removal of 1.7 mM MgCl2 to the Mg2(+)-free perfusate produced a reversible decrease (20%) in basal EC DA levels. This decrease may reflect a competitive interaction between Ca2+ and Mg2+ in the process of vesicular release. Basal EC DA levels were also reduced (27%) by decreasing the K+ concentration of the perfusate from 4 mM to 3 mM. However, after restoring the K+ concentration to 4 mM, EC DA levels were slow to return to pretreatment levels. Basal EC 3,4-dihydroxyphenylacetic acid and homovanillic acid levels exhibited a parallel but diminished response to each manipulation of the ionic concentration of the perfusate. This study demonstrates that small variations in the concentrations of Ca2+, Mg2+, and K+ in the perfusate employed in microdialysis preparations will affect basal EC striatal DA and metabolite levels.     

Using Magnetically Responsive Tea Waste to Remove Lead in Waters under Environmentally Relevant Conditions

We report the use of a simple yet highly effective magnetite-waste tea composite to remove lead(II) (Pb²⁺) ions from water. Magnetite-waste tea composites were dispersed in four different types of water–deionized (DI), artificial rainwater, artificial groundwater and artificial freshwater–that mimic actual environmental conditions. The water samples had varying initial concentrations (0.16–5.55 ppm) of Pb²⁺ ions and were mixed with the magnetite-waste tea composite for at least 24 hours to allow adsorption of the Pb²⁺ ions to reach equilibrium. The magnetite-waste tea composites were stable in all the water samples for at least 3 months and could be easily removed from the aqueous media via the use of permanent magnets. We detected no significant leaching of iron (Fe) ions into the water from the magnetite-waste tea composites. The percentage of Pb adsorbed onto the magnetite-waste tea composite ranged from ∼70% to 100%; the composites were as effective as activated carbon (AC) in removing the Pb²⁺ ions from water, depending on the initial Pb concentration. Our prepared magnetite-waste tea composites show promise as a green, inexpensive and highly effective sorbent for removal of Pb in water under environmentally realistic conditions.     

A comparison of ATP-degrading enzyme activities in rat incisor odontoblasts.

In active odontoblasts from the rat incisor, used as a model system for biologic calcification, two distinguishable enzyme activities capable of degrading adenosine monophosphate (ATP) exist. Once can be inhibited ny 1-tetramisole, (+/-)-2,3,5,6,-tetrahydro-6-phenylimidazo (2.1B) THIAZOLE HYDROCHLORIDE (Levamisol) and (+/-)-6(m-bromophenyl)-5.6-dehydroimidazo (2.1-b) thiazole oxalate (R823) and is probably identical with nonspecific alkaline phosphatase (EC 3.1.3.1). The activity of the other enzyme, named Ca2+-ATPase, is dependent on the presence of Ca2+ or Mg2+ and is activated by these ions. The pH optimum of Ca2+-ATPase is 9.8. The Ca2+-ATPase is unaffected by Levamisole, R 8231, ouabain, ruthenium red, Na+ and K+ ions. Maximal activity was found against ATP, whereas adenosine diphosphate, guanosine triphosphate, inosine triphosphate and adensoine monophosphate were hydrolysed at lower rate. It may be speculated that the Ca2+-ATPase is concerned with the transmembranous transport of Ca2+ ions to the mineralization front.