Determination of cadmium(II), copper(II), manganese(II) and nickel(II) species in Antarctic seawater with complexing resins   总被引：1，自引：0，他引：1  

Raffaela Biesuz  Giancarla Alberti  Girolamo D'Agostino  Emanuele Magi  Maria Pesavento 《Marine Chemistry》2006,101(3-4):180-189

The strong species of cadmium(II), copper(II), manganese(II) and nickel(II) in an Antarctic seawater sample are investigated by a method based on the sorption of metal ions on complexing resins. The resins compete with the ligands present in the sample to combine with the metal ions. Two resins with different adsorbing strengths were used. Very stable metal complexes were investigated with the strong sorbent Chelex 100 and weaker species with the less strong resin, Amberlite CG-50. Strong species were detected for three of the considered metal ions, but not for Mn(II). Cu(II) is completely linked to species with a side reaction coefficient as high as log α_M(I) = 11.6 at pH = 7.3. The ligand concentration was found to be similar to that of the metal ion, and the conditional stability constant was around 10²⁰ M^− 1. In the considered sample, only a fraction of the metal ions Cd(II) and Ni(II) is bound to the strong ligands, with side reaction coefficients equal to log α_M(I) = 5.5 and 6.5 at pH = 7.3 for Cd(II) and Ni(II), respectively. These findings were confirmed by the test with the weaker sorbent Amberlite CG-50. It can be calculated from the sorption equilibria that neither Mn(II) nor Ni(II) is adsorbed on Amberlite CG-50 under the considered conditions and, in fact, only a negligible fraction of Mn(II) and Ni(II) was adsorbed. A noticeable fraction of Cd(II) was adsorbed on Amberlite CG-50, meaning that cadmium(II) is partially linked to weak ligands, possibly chloride, while no copper(II) was adsorbed on this resin, confirming that copper(II) is only combined in strong species. These results are similar, but not identical, to those obtained for other seawater samples examined in previous investigations.  相似文献   

重金属离子对日本蟳血淋巴抗氧化酶（SOD，CAT，GPx）活力的影响     

《中国海洋大学学报(自然科学版)》2006,36(B05):49-53

  相似文献   

硒(Ⅳ)-氯化四苯胂盐酸盐络合物的吸附波及其应用     

魏显有 《岩矿测试》1991,(1)

本文研究了在HCl介质中,Se(Ⅳ)-氯化四苯胂络合物的极谱行为。在0.05mol/LHCl溶液中,该络合物于-0.58V(vs.SCE)处出现灵敏的吸附波。Se的检测下限可达0.0001μg/ml。本文拟定的方法应用于天然水中痕量Se的直接测定,结果良好。  相似文献   

Initial interpretation of Titan plasma interaction as observed by the Cassini plasma spectrometer: Comparisons with Voyager 1     

R.E. Hartle  E.C. Sittler  R.E. Johnson  F. Crary  D.T. Young  D. Simpson  D. Reisenfeld  J.J. Berthelier  J. Vilppola  N. Andre 《Planetary and Space Science》2006,54(12):1211-1224

The Cassini plasma spectrometer (CAPS) instrument made measurements of Titan's plasma environment when the Cassini Orbiter flew through the moon's plasma wake October 26, 2004 (flyby TA). Initial CAPS ion and electron measurements from this encounter will be compared with measurements made by the Voyager 1 plasma science instrument (PLS). The comparisons will be used to evaluate previous interpretations and predictions of the Titan plasma environment that have been made using PLS measurements. The plasma wake trajectories of flyby TA and Voyager 1 are similar because they occurred when Titan was near Saturn's local noon. These similarities make possible direct, meaningful comparisons between the various plasma wake measurements. They lead to the following: (A) The light and heavy ions, H⁺and N⁺/O⁺, were observed by PLS in Saturn's magnetosphere in the vicinity of Titan while the higher mass resolution of CAPS yielded H⁺ and H₂⁺as the light constituents and O⁺/CH₄⁺ as the heavy ions. (B) Finite gyroradius effects were apparent in PLS and CAPS measurements of ambient O⁺ ions as a result of their absorption by Titan's extended atmosphere. (C) The principal pickup ions inferred from both PLS and CAPS measurements are H⁺, H₂⁺, N⁺, CH₄⁺ and N₂⁺. (D) The inference that heavy pickup ions, observed by PLS, were in narrow beam distributions was empirically established by the CAPS measurements. (E) Slowing down of the ambient plasma due to pickup ion mass loading was observed by both instruments on the anti-Saturn side of Titan. (F) Strong mass loading just outside the ionotail by a heavy ion such as N₂⁺ is apparent in PLS and CAPS measurements. (G) Except for the expected differences due to the differing trajectories, the magnitudes and structures of the electron densities and temperatures observed by both instruments are similar. The high-energy electron bite-out observed by PLS in the magnetotail is consistent with that observed by CAPS.  相似文献   

Study on changes of plasmalemma permeability and some primary inorganic ions of Antarctic ice microalgae （Chlamydomonas sp. ICE-L） in the low-temperature stress     

郑洲  缪锦来陈豪张波涛  李光友 《极地研究(英文版)》2006,17(1):20-29

The changes of plasmalemma permeability and some primary inorganic ions of Antarctic ice microalgae （ Chlamydomonas sp. ICE-L） in the low-temperature stress were examined. The plasmalemma of 1CE-L could maintain the stability at the freezing condition of -6 ℃. That signifies that it could maintain the proper function of plasmalemma and stability of the intracellular environment during sea ice formation. The function of inorganic ions on low-temperature adaptation of ICE-L was investigated by using the X-ray microanalysis method. Low temperature （0 - -6 ℃ ） induces Ca^2 ＋ concentration increment of cytoplasm, but after 24 h the content decrease quickly to normal value. As a matter of fact, Ca^2 ＋ plays an important role as the second messenger in the low temperature adaptation of ICE-L. In addition, low temperature also influences on the other primary inorganic ions transfer and the cell maintains activity by keeping ratio balance among different ions. Above all, it is necessary for Antarctic ice microalgae to survive and breed by maintaining the stability of K^ ＋ content and the balance of Na^ ＋/Cl^ -.  相似文献   

Spectrum characteristics of major ion concentrations at Wuhan sectoin of the Changjiang Rriver     

Xing-hui Xia  Jing-sheng Chen  Xu-yi Cai 《中国地理科学(英文版)》2001,11(4):315-320

Spectrum analyses of water quality time series have been carried out for five hydrometric stations including Wuhan hydrometric station of the Changjiang(Yangtze) River, etc. The fluctuations of Ca²⁺, Mg²⁺ and HCO ₃ ⁻ concentrations in river water under different physical geography conditions have about two-year cycle which is corresponding to hydrometeorological quasi-biannual-oscillation (QBO). Na⁺, Cl⁻ SO ₄ ²⁻ have about two-year cycle in the area lightly affected by human activities while two-year cycle doesn’t exist in the area heavily affected by human activities. All the fluctuations of major ions have about three-month cycle. The river diseharge fluctuation accounts for 43.9%, 45.1%, 54.3%, 33.9%, 30.3% and 42.7% of the variance of Ca²⁺, Mg²⁺, HCO ₃ ⁻ , Na⁺, Cl⁻, SO ₄ ²⁻ , respectively, at Wuhan from 1962 to 1985. According to the spectrum characteristic of major ions, the duration of the time series has to be at least 13 years for trend analysis of monthly water quality data. Foundation item: Under the auspices of the National Natural Science Foundation of China (No. 49671017). Biography: XIA Xing-hui(1971-), female, a native of Hunan Province, Ph. D. Her research interest includes environmental chemistry.  相似文献   

Spatial and seasonal variation of major ions in Himalayan snow and ice: A source consideration   总被引：2，自引：0，他引：2  

Ya-ping Liu  Zhi-xing Geng  Shu-gui Hou   《Journal of Asian Earth Sciences》2010,37(2):195-205

The spatial and temporal variation of major ions (Ca²⁺, Mg²⁺, Na⁺, K⁺, , , and Cl⁻) in Himalayan snow and ice is investigated by using two snow pits from the East Rongbuk glacier (28°01′N, 86°58′E, 6500 m a.s.l.), one snow pit from the Nangpai Gosum glacier (28°03′N, 86°39′E, 5700 m a.s.l.), one snow pit from the Gyabrag glacier (28°11′N, 86°38′E, 6303 m a.s.l.), and three ice cores from the Sentik (35°59′N, 75°58′E, 4908 m a.s.l.), Dasuopu (28°33′N, 85°44′E, 7000 m a.s.l.), and East Rongbuk (27°59′N, 86°55′E, 6450 m a.s.l.) glaciers, respectively. In general, the major ions show a significant seasonal variation, with high concentrations during the non-monsoon (pre-monsoon and post-monsoon) season and relatively low concentrations during the monsoon season. Monsoon precipitation with high local/regional dust loading related to summer circulation is possibly responsible for the high concentrations occurring sporadically during the monsoon season. The crest of the Himalayas is an effective barrier to the spatial distribution of Na⁺, Cl⁻ and concentrations, but not to the major ions associated with dust influx (e.g. Ca²⁺ and Mg²⁺). Atmospheric backward trajectories from the HYSPLIT_4 model used in identifying chemical species sourcing suggest that the major ions in the Himalayan snow and ice come mainly from the Thar Desert located in the North India, as well as West Asia, or even the distant Sahara Desert in the North Africa during the winter and spring seasons. This is different from the conventionally assumed arid and semi-arid regions of the central Asia. Factors, such as different vapor sources due to atmospheric circulation patterns and geographical features (e.g. altitude, topography), may contribute to the differences in major ionic concentrations between the western and eastern Himalayas.  相似文献   

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     

朱翔  徐志鹏  罗一单  彭福全  庞晴晴  谢磊  马玉珅  汪龙眠 《湖泊科学》2022,34(3):843-854

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.  相似文献   

An Acetic Acid‐Based Extraction Protocol for the Recovery of U,Th and Pb from Calcium Carbonates for U‐(Th)‐Pb Geochronology     

Andrew J. Mason  Gideon M. Henderson  Anton Vaks 《Geostandards and Geoanalytical Research》2013,37(3):261-275

A new method for the simultaneous recovery of U, Th and Pb from ca. 0.5 g calcium carbonate samples for the purpose of U‐(Th)‐Pb geochronometry is presented. The protocol employs ion‐exchange chromatography. Standard anion exchange resin (AG 1‐X8 100–200 mesh) was used as the static phase, and 90% acetic acid was used as the mobile phase to elute the unwanted matrix components; dilute nitric acid was used to elute the U, Th and Pb. Blanks of 1.8 pg Th, 6.4 pg Pb and 8.4 pg U were obtained. The protocol was evaluated by determining the isotopic composition of U‐Th‐Pb separates obtained from an in‐house reference material (prepared from a natural speleothem) by MC‐ICP‐MS. An independently dated speleothem was also reanalysed. Based on these tests, the extraction protocol had an acceptable blank and produced a Pb separate sufficiently free of matrix‐induced instrumental biases to be appropriate for U‐Th‐Pb chronology.  相似文献   

金刚石呈色机制的新观点     

彭明生  蒙宇飞  杨志军 《矿物学报》2003,23(3):211-215

已知金刚石中能产生颜色的点缺陷(即色心)主要有氮、硼、空穴、填隙子以及各种形式的氮与空穴的复合体。随着各种现代微束与谱学分析技术以及量子化学计算的应用，对金刚石晶格中氮、硼以外的杂质—氢与过渡金属离子的赋存状态的研究，我们发现了新的致色点缺陷：成键氢，镍、钴离子，及其与氮的复合体，从而形成了氢致色与过渡金属离子致色的金刚石呈色机制的新观点。  相似文献