合浦珠母贝贝壳珍珠层EDTA可溶性基质蛋白对无定形碳酸钙稳定性的影响

通过红外光谱、扫描电镜、能谱等方法探讨了合浦珠母贝贝壳珍珠层EDTA可溶性基质蛋白(ESM)对无定形碳酸钙(ACC)晶型转化的影响。试验结果显示,合浦珠母贝贝壳珍珠层ESM在镁离子存在的条件下能够显著抑制ACC的转化,并减少最终诱导形成的方解石中的镁离子含量。同时,珍珠层ESM具有调节方解石晶体晶貌的作用。     

金属离子种类对珊瑚砂微生物固化影响研究

选用巴斯德芽孢杆菌,对微生物诱导钙离子、镁离子以及铁离子形成碳酸盐固化松散珊瑚砂颗粒的效果进行对比研究。试验结果表明,在相同试验方法、相同注入次数的条件下,微生物诱导形成的碳酸钙和碳酸镁能将珊瑚砂松散颗粒固化成为整体,加入铁离子的试样因为反应过程的原因没有成功。通过渗透性、干密度变化、无侧限抗压强度及微观结构等方面进行对比分析,钙离子试样相对于镁离子试样,具有固化过程平稳、干密度增量大、强度高、微观颗粒包裹更好的优点。综合试验结果得出,钙离子是现阶段微生物固化珊瑚砂较为理想的金属离子。本试验首次探讨了金属离子种类对珊瑚砂微生物固化效果的影响,为微生物固化技术提供了一定理论基础,对该技术的进一步应用具有一定借鉴意义。     

铜和镁离子对卵圆卡盾藻生长、光合色素和溶血活性的影响

本研究探索了不同浓度的铜和镁离子对卵圆卡盾藻(Chattonella ovata)光合色素含量及其溶血活性的影响,并探讨了溶血活性与光合色素间的关系。结果表明,当铜和镁离子浓度分别为7.84μg/dm~3和18.79 g/dm~3时,卵圆卡盾藻达到最佳生长状态。不同浓度的铜离子(3.92、5.88、7.84、9.80μg/dm~3)处理下,高浓度组(9.80μg/dm~3)抑制了卵圆卡盾藻岩藻黄质和硅甲藻黄素的积累。随着镁离子浓度(7.52、11.27、15.03、18.79 g/dm~3)的增加,叶绿素c2和硅甲藻黄素的平均含量增加,而紫黄质、岩藻黄质平均含量变化不显著(p 0.05)。卵圆卡盾藻的溶血活性均随金属离子浓度升高而增强,与叶绿素c2的变化趋势一致。对溶血活性与光合色素进行因子分析,提示溶血毒素与叶绿素c2密切相关,这种毒素可能是叶绿素c2或其类似物。     

浓海水冷冻脱盐技术研究

通过实验室冷冻离心实验,研究了浓海水的冷冻脱盐技术.实验研究了离心转速对冰冻的浓海水的脱盐和脱除钙镁离子的影响,并对多步冷冻脱盐前后余冰和浓海水的盐度分别进行分析,以及利用ICP-MS对其主要离子含鼍进行测定.实验结果表明,离心转速变化对冰冻浓海水脱盐、脱除钙镁离了的影响显著.各实验离心转速条件下,脱盐和脱除钙镁离了均有较好效果.脱除率均达到88.5%和87.4%以上.随着离心转速的提高,脱盐率提高,转速4 000 r/min达到最大,但是其变化幅度减小,进一步提高转速对脱盐率和钙镁离子脱除率的提高影响不大.经过多步冷冻脱盐发现,一次冷冻离心分离,得到的余冰的盐度脱除达到99.0%.通过与原浓海水离子含量相比,钾钙钠镁等主要离子含量降低为原浓海水的3%以下.而多步离心分离之后,得到的浓海水的盐度达到原浓海水的3.3倍.每步实验,均有低盐度,低离子含量的冰生成,冰的产最达到被处理的浓海水总体积的2/3以上.     

保存液中Ca2+、Mg2+、K+对中华绒螯蟹（Eriocheir sinensis）精子体外保存存活率的影响

提要以伊红染色法检测样品精子存活率为依据,研究了4℃下5种保存液及Ca2 、Mg2 离子对中华绒螯蟹精子体外保存效果的影响。5种保存液分别为人工海水(ASW)、2倍钙离子人工海水(2×Ca2 -ASW)、无镁离子人工海水(Mg2 -FASW)、无钾离子人工海水(K -FASW)、无钙离子人工海水(Ca2 -FASW),经4天保存后,各保存液中精子样品的存活率和精子密度均出现明显差异,K -FASW、ASW及2×Ca2 -ASW三种保存液中的精子因发生顶体反应而大量死亡,而Mg2 -FASW、Ca2 -FASW的保存效果较好。在此基础上,进一步探讨了不同Mg2 和Ca2 浓度对精子存活率的影响,结果发现,经24h保存后各实验组精子存活率均随着两种离子浓度的增加而明显下降。上述结果表明:K -FASW、ASW及2×Ca2 -ASW不适合精子保存,而Mg2 -FASW和Ca2 -FASW均可作为该蟹精子的保存液;Ca2 因可引起精子顶体反应而造成保存液中精子的大量死亡,其浓度与存活率呈明显的负相关;无K 的保存液中,Ca2 、Mg2 的存在与否对精子的保存效果起关键作用;无Mg2 人工海水之所以具有较好的保存效果,可能与Mg2 的缺乏而导致Ca2 逆浓度差转运受阻,避免了因Ca2 进入而诱发顶体反应有关。     

山东半岛南部近海大气气溶胶水溶性离子的化学组成

为研究陆源输入对中国近海大气气溶胶的影响,于2007年春季和秋季对山东半岛南部近海进行气溶胶采集工作.分析结果表明气溶胶水溶性离子中主要无机离子无显著的季节性变化,其中二次离子(nss-SO2-4,NO-3,NH+4)浓度最高,占总测定离子浓度的80%以上.甲磺酸离子浓度春季明显高于秋季,分别为(0.041±0.022)和(0.012±0.003 1)μg·m-3,导致生源硫酸盐对非海盐硫酸盐的贡献率分别为4.5%和1.5%;另一方面海盐源硫酸盐分别占总硫酸盐浓度的3.3%和3.9%,以上结果表明人为输入源占山东近海大气气溶胶中硫酸盐来源的主要部分.春季与秋季气溶胶中nss-SO2-4/NO-3值分别为1.43和1.34,反映出近年来中国大气中SO2/NOx呈现出下降趋势.由此可见,来自陆源的人为活动输送导致山东南部近海大气气溶胶的化学组成呈现出明显的陆源特征.     

三疣梭子蟹(Portunus trituberculatus)含新型关键识别基序DPY/WTD单结构域C型凝集素PtCTL-6的免疫功能研究

C型凝集素是一类依赖于钙离子的糖识别蛋白超家族,该家族蛋白在海洋无脊椎动物先天免疫系统中的非己识别和对病原微生物的清除过程中起重要作用。本文以三疣梭子蟹(Portunus trituberculatus)含单个糖识别域(CRD)的C型凝集素PtCTL-6为研究对象展开研究。研究表明PtCTL-6的开放阅读框(ORF)编码一条由信号肽、LDLa和CRD组成的多肽链。该C型凝集素的识别关键基序为DPY/WTD(Asp-Pro-Tyr/Trp-Thr-Asp),未见于前人研究。病原相关分子模式(PAMPs)结合活性检测结果表明:PtCTL-6重组蛋白(rPtCTL-6)能结合脂多糖(LPS)、肽聚糖(PGN)和β-葡聚糖(β-glucan),并能结合7种微生物,包括革兰氏阴性菌、革兰氏阳性菌和真菌。凝菌活性实验证明, PtCTL-6能选择性地凝集真菌毕赤酵母(Pichiapastoris)与酿酒酵母(Saccharomycescerevisiae)。以上结果证实PtCTL-6能作为模式识别受体参与机体对微生物的识别,并且该分子具备较广泛的免疫识别谱。最后,本文初步探索了该分子对"非己"物质的识别机制,发现PtCTL-6通过特异性的结合D-甘露糖和D-岩藻糖对"非己"物质进行识别,是一种具备新型糖结合模式的C型凝集素。     

浒苔化学成分研究

利用硅胶柱色谱、Sephadex LH-20柱色谱和HPLC等手段,从浒苔Entermorpha prolifera的甲醇提取物中分离得到了5个单体化合物。它们的结构通过波谱分析结合文献对照被鉴定为:胆甾醇(1),132S-羟基脱镁叶绿素a(2),132R-羟基脱镁叶绿素a(3),132S-羟基脱镁叶绿素b(4),phaeophytin a hydroperoxide(5)。化合物2~5均为首次从该种海藻中分离得到。     

氟镁离子对形成常数的测定

海水主要成份的存在状态,对于海洋地球化学及海洋生物过程有重要的影响。近年来,已引起人们的重视。当要求定量地了解海水中各成份存在状态时,因不易直接测定,通常多采用形成常数计算法。在计算中,如果采用的形成常数不同时,结果也不相同。因此,在计算海水主要成份的存在状态时,首先需要正确的形成常数。关于氟镁离子对形成常数(K_(MgF~ ))的测定,已有一些报导。本文使用氟离子选择电极测定了氟镁离子对形成常数。离子选择性电极是近年来迅速发展起来的一种新的分析测量工具,可以通过简单的电势测量直接测定溶液中某一离子的活度,这种测量所用的设备简     

混合暴露条件下刺参(Apostichopus japonicus)对重金属的富集与释放特征

应用双箱动力学模型模拟了刺参在Pb、Zn、Cu、Cd、Cr、Hg和As 7种重金属混合暴露条件下,呼吸树、消化道和体壁组织对重金属的生物富集与释放实验。结果表明:(1)重金属在刺参组织器官中的富集具有选择性,理论平衡状态下,As、Cd、Cr在各组织的含量分布(CAmax):呼吸树消化道体壁,Cu、Zn分布规律(CAmax):消化道呼吸树体壁,Hg、Pb分布规律(CAmax):体壁呼吸树消化道。(2)刺参对不同重金属的富集系数存在显著差异(P0.05),呼吸树组织对Cr离子富集系数最高2298.2,其次是Cu、Cd离子,其BCF均在1500以上,Hg、Pb、Zn和As离子在呼吸树中的富集系数较低。体壁对Cu离子的富集系数最高为1560.7,对As离子富集系数最低52.7。消化道对Cu离子富集系数最高6037,对As离子富集系数最低为87.9。     

Stability of the calcium sulphate ion pair at the ionic strength of seawater by potentiometry

The stability of the ion pair CaSO₄ was determined from measurement of the change in calcium ion activity with medium composition at constant ionic strength. A calcium selective PVC-matrix liquid membrane electrode was used to monitor the calcium ion activity. All measurements were performed at 1 atm, 25 ± 0.1°C and 0.7 M formal ionic strength. The evaluation of the stability constant depends on the degree of complexation between calcium and chloride and between sodium and sulphate. The dependence of K_CaSO4, on K_NaSO4 and K_CaCl can be described by the following relations:K_CaSO4=17.7 K_CaCl+16.5 (K_NaSO4=1.8)K_CaSO4=18.8 K_CaCl+17.3 (K_NaSO4=2) for K_CaCl=0–1A value of K_CaSO4=25.4 is suggested.     

可口革囊星虫(Phascolosoma esculenta)重组铁蛋白富集Pb2+等重金属特性和功能研究

利用可口革囊星虫重组铁蛋白富集Pb²⁺、Fe³⁺、Cd²⁺、Cr³⁺、Cu²⁺、Mn²⁺、Sn²⁺和Zn²⁺等8 种重金属离子后, 通过透射显微镜和傅里叶红外光谱测定蛋白的超微结构变化和内部基团特性。以 天然的马脾铁蛋白为对照, 观察重组铁蛋白与天然铁蛋白的差别。结果显示, 重组铁蛋白富集Pb²⁺ 和其它7 种重金属离子后蛋白体积大小与重金属离子种类直接相关。重组铁蛋白相对天然铁蛋白来 说在富集不同种类重金属离子后, 除了非特异性酰胺特征峰和蛋白特征峰外, 还出现一些专门富集 某些重金属离子的特异基团, 如:-CH₃、-CH₂-、-CH-、-NH-、-SO₃-、-COOH、-S=S-和-C-S-C 等。 通过细胞实验进一步验证了铁结合蛋白能够通过富集重金属离子Pb²⁺来保护小鼠成骨前体细胞 MRC3T3-E1, 使细胞的死亡率明显降低(P<0.05).     

Study of magnesium precipitation based on biocementation

Abstract

Magnesium carbonate has a cementing character like calcium carbonate, and the addition of magnesium ion enables the microbe cementitious material to have the denser microstructure with the lower porosity. The effects of various factors, such as the concentration of Ca²⁺ and Mg²⁺, on the urease activity were studied. Comparison of the productive rates for calcium carbonate and magnesium carbonate were carried out, as well as productive rates for magnesium carbonate with adding different amount of urea to medium. Calcium acetate and magnesium acetate were, respectively, used for sands solidification. Results showed that the increase in urea concentration and magnesium ion enhanced urease activity, while calcium ion significantly impaired urease activity. Sodium chloride and acetate ion had little influence on it. Productive rates for magnesium carbonate were dramatically smaller than its calcium counterpart. However, adding urea to medium allowed for more magnesium precipitation, and the higher the urea concentration, the more the magnesium precipitation. The sand columns with adding urea to medium can have a high strength despite using magnesium acetate. Therefore, the method could solve the problem of insufficient magnesium precipitation. The results will act as a guide for the application of biocementation technology with magnesium carbonate.     

Formation and stability of mixed Mg/Ca/phytate species in synthetic seawater media: Consequences on ligand speciation

The results of a potentiometric investigation (by ISE-H⁺, glass electrode) on the speciation of phytate ion (Phy¹²⁻) in an ionic medium simulating the major components (Na⁺, K⁺, Ca²⁺, Mg²⁺, Cl⁻ and SO₄²⁻) of natural seawater, at different salinities and t = 25 °C, are reported. The work was particularly aimed at determining the possible formation of mixed Ca²⁺–Mg²⁺–phytate ion pairs, and to establish how including the formation of these mixed species would affect the speciation modeling in seawater media. After testing various speciation models, that considering the formation of the MgCaH₃Phy⁵⁻, MgCaH₄Phy⁴⁻, Mg₂CaH₃Phy³⁻ and Mg₂CaH₄Phy²⁻ species was accepted, and corresponding stability constants were determined at two salinities (S = 5, 10). A discussion is reported both on the choice of the experimental conditions and on the possibility to extend these results to those typical of real seawater. A detailed procedure is also described to demonstrate that the stability of these species is higher than that statistically predicted. As reported in literature, a parameter, namely log X, has been determined in order to quantify this extra stability for the formation of each mixed species at various salinities. For example, at S = 10, log X₁₁₃ = 2.67 and log X₁₁₄ = 1.37 for MgCaH₃Phy⁵⁻ and MgCaH₄Phy⁴⁻ (statistical value is log X_stat = 0.60), and log X₂₁₃ = 6.11 and log X₂₁₄ = 2.15 for Mg₂CaH₃Phy³⁻ and Mg₂CaH₄Phy²⁻ (log X_stat = 1.43), respectively. Results obtained also showed that the formation of these species may occur even in conditions of low salinity (i.e. low concentration of alkaline earth cations) and low pH (i.e., more protonated ligand).     

Behaviour of boron,calcium and magnesium in a polluted estuary

Behaviour of industrially added boron in the well mixed Ambika river estuary of South Gujarat, India has been studied along with that of calcium and magnesium. The ratios of Ca : Cl and Mg : Cl at varying chlorinities were always within the normal ranges found in river water at one end and seawater at the other end. B : Cl exceeded the river water end limit at the ebb tide at an upstream station. Percentage addition or removal of boron, calcium and magnesium was calculated using the concept of the theoretical dilution line. The external input raised the boron concentration by 263% in the vicinity of the industrial discharge. A correlation coefficient of ?0·82 between chlorinity and percentage addition or removal of boron supports the theory of boron incorporation in sediments in amounts proportional to salinity. Inverse relationship between percentage addition or removal of boron and suspended solids was observed. Behaviour of calcium and magnesium was in line with the replacement of Ca²⁺ ions occupying the majority of ion-exchange sites in riverine clays by Mg²⁺, Na⁺ and K⁺ during their first encounter with seawater.     

极大螺旋藻富积重金属机理的研究

于1993年5月由南京大学藻类培养室提供极大螺旋藻藻种,用Zarrouk培养基培养后,用活藻体和甲醛杀死的藻体分别进行吸附实验;过滤出的藻体置于6×10－3g／L左右浓度的Co2+,Ni2+,Cu2+,Zn2+离子混合液中。结果显示,死、活藻体都具有相似的吸附能力,对Co2+,Ni2+,Zn2+的富积大于203倍,对Cu2+的富积大于185倍;用热水提取、DEAE-纤维素D-23柱和SephadexG－200柱纯化后,获得了纯细胞外壁多糖,其分子量为52kD。将该糖溶液盛在透析袋内,并置于4种离子混合液中进行吸附实验,结果显示,核糖对Co2+,Ni2+,Cu2+,Zn2+的富积倍数分别达1744,1644,1340,1750。藻体和多糖对Co2+,Ni2+,Zn2+的吸附都高于对Cu2+的吸附。比较藻体与多糖对4种离子的吸附结果可见,藻体对离子的吸附主要是多糖的作用;多糖的红外光谱显示,金属离子改变OH和CO－NH的吸收峰,表明这两种基团与金属离子发生了络合作用;对Cu2+的络合滴定测定表明,Cu2+与多糖的结合度为0．40。     

The speciation of Fe(II) and Fe(III) in natural waters

The interactions of Fe(II) and Fe(III) with the inorganic anions of natural waters have been examined using the specific interaction and ion pairing models. The specific interaction model as formulated by Pitzer is used to examine the interactions of the major components (Na⁺, Mg²⁺, Ca²⁺, K⁺, Sr²⁺, Cl⁻, SO₄⁻, HCO₃⁻, Br⁻, CO₃²⁻, B(OH)₄⁻, B(OH)₃ and CO₂) of seawater and the ion pairing model is used to account for the strong interaction of Fe(II) and Fe(III) with major and minor ligands (Cl⁻, SO₄²⁻, OH⁻, HCO₃⁻, CO₃²⁻ and HS⁻) in the waters. The model can be used to estimate the activity and speciation of iron in natural waters as a function of composition (major sea salts) and ionic strength (0 to 3 M). The measured stability constants (K_FeX^*) of Fe(II) and Fe(III) have been used to estimate the thermodynamic constants (K_FeX) and the activity coefficient of iron complexes (γ_FeX) with a number of inorganic ligands in NaClO₄ medium at various ionic strengths: In(K_FeX/γ_Feγ_X) = InK_FeX − In(γ_FeX) The activity coefficients for free ions (γ_Fe, γ_x) needed for this extrapolation have been estimated from the Pitzer equations. The activity coefficients of the ion pairs have been used to determine Pitzer parameters (B_FeX, B_FeX⁰, C_FeX^φ) for the iron complexes. These results make it possible to estimate the stability constants for the formation of Fe(II) and Fe(III) complexes over a wide range of ionic strengths and in different media. The model has been used to determine the solubility of Fe(III) in seawater as a function of pH. The results are in good agreement with the measurements of Byrne and Kester and Kuma et al. When the formation of Fe organic complexes is considered, the solubility of Fe(III) in seawater is increased by about 25%.     

Ion association of chloride and sulphate with sodium,potassium, magnesium and calcium in seawater at 25°C

Stoichiometric association constants, which have been measured for the ion pairs of Cl^? and SO₄^?2 with Na⁺, K⁺, Mg²⁺, and Ca²⁺, were used to determine the speciation in an artificial sea water containing only these ions. The resulting distribution is quite different to that found in earlier models in which chloride ion association was ignored. The concentrations of chloride ion pairs with the cations are 4 to 5 times larger than the concentrations of the sulphate ion pairs with the same cations. The total activity coefficients of the neutral salts in sea water calculated from the model are in good agreement with the experimentally measured values. The concentration of MgSO₄⁰ calculated to be present agrees with the amount determined from ultrasonic absorption data. The calculated solubility of gypsum is also in good agreement with the measured values.     

Luminescence quenching of dissolved organic matter in seawater

To characterize more fully the nature of the fluorophores present in the dissolved organic matter found in seawater, steady state and time-resolved measurements of the luminescence quenching of a number of samples of marine dissolved organic matter with known quenchers, such as iodide, acrylamide and methyl viologen (MV) (1,1′-dimethyl-4,4′-bipyridinium), were compared. Quenching characteristics of these systems were analyzed using Stern-Volmer plots for both intensity and lifetime measurements. The bimolecular quenching constants, κ_q, for these quenchers were found to decrease in the order MV²⁺ (κ_q 10¹⁰M⁻¹s⁻¹) > I⁻ (κ_q 2 × 10⁹ M⁻¹ s⁻¹) >CH₂CHCONH₂ (κ_q 2 × 10⁸ M⁻¹ s⁻¹) for the samples measured. The results also show that different samples are quenched to differing extents by the quenchers studied, that ionic strength alters the quenching constants, and that both static and diffusional quenching mechanisms may operate.Such studies are appropriate to the quantification of the reactivity of the singlet states of the chromophores found within marine dissolved organic matter. Although excess energy of the singlet state may be readily transferred to another chemical species, the combination of competing physical deactivation paths and the low concentrations of efficient quenches in the oceans serves to lessen the direct chemical impact of this process.