Nitrogen uptake,ammonium oxidation and nitrous oxide (N2O) levels in the coastal waters of western Cook Strait,New Zealand

Vertical measurements of $\text{NH}{}_4{}^{\mathrm{+}}$, $\text{NO}{}_3{}^{\mathrm{?}}$ and N₂O concentrations, $\text{NO}{}_3{}^{\mathrm{?}}$ and $\text{NH}{}_4{}^{\mathrm{+}}$ uptake, and $\text{NH}{}_4{}^{\mathrm{+}}$ oxidation rates were measured at 5 sites in western Cook Strait, New Zealand, between 31 March and 3 April 1983. Nitrate increased with depth at all stations reaching a maximum of 10.5 μg-atom $\text{NO}{}_3{}^{\mathrm{?}}\text{N l}{}^{\mathrm{?1}}$ at the most strongly stratified station whereas $\text{NH}{}_4{}^{\mathrm{+}}$ was relatively constant with depth at all stations (～0.1 μg-atom $\text{NH}{}_4{}^{\mathrm{+}}\text{N l}{}^{\mathrm{?1}}$). The highest rates of $\text{NH}{}_4{}^{\mathrm{+}}$ oxidation generally occurred in the near surface waters and decreased with depth. N₂O levels were near saturation with respect to the air above the sea surface and showed no obvious changes during 24 h incubation. $\text{NH}{}_4{}^{\mathrm{+}}$ oxidation by nitrifying bacteria may account for about 30% of the total $\text{NH}{}_4{}^{\mathrm{+}}$ utilization (i.e. bacterial+agal) and, assuming oxidation through to $\text{NO}{}_3{}^{\mathrm{?}}$, may supply about 40% of the algal requirements of $\text{NO}{}_3{}^{\mathrm{?}}$ in the study area. These results suggest that bacterial nitrification is of potential importance to the nitrogen dynamics of the western Cook Strait, particularly with respect to the nitrogen demands of the phytoplankton.     

Determination of cadmium(II), copper(II), manganese(II) and nickel(II) species in Antarctic seawater with complexing resins

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.     

A Laboratory and Theoretical Study on the Uptake of SO2 Gas by Large and Small Water Drops Containing Heavy Metal Ions

Laboratory experiments have been carried out to investigate the uptake of sulfur dioxide by water drops containing heavy metal ions where the metal ions serve as catalysts to oxidise the taken up S(IV) into S(VI). During the gas uptake the drops were freely suspended at their terminal velocity in the airstream of the Mainz vertical wind tunnel. Two series of experiments were carried out, one with large millimeter size water drops containing manganese or iron ions, and the other with small water drops containing manganese ions and having radii in hundreds of micron size range. The experimental results were compared against model computations using the Kronig–Brink model and the fully mixed model, modified for the case that heavy metal ions present in the liquid phase act as catalysts for the oxidising process. The results of the model calculations show that there are only small differences between the predicted gas uptake according to the two models. In addition it was found that the experimental obtained results from the uptake of SO₂ by water drops containing heavy metal ions for both, large and small water drops did agree with the model results.     

闪电首次回击过程的光谱特性

用无狭缝摄谱仪，拍摄了4次云对地闪电首次回击过程390一660nm波长范围的光谱，并将原子结构的理论应用于闪电光谱的研究，用多组态Dirac—Fock方法，系统考虑相对论效应、电子关联、弛豫效应等重要贡献，对光谱的精细结构进行了计算，给出了谱线的波长、振子强度以及相应的上能级激发能量。通过与试验观测谱线的比较分析发现，大多数谱线对应的上激发能在23ev左右。首次回击过程中，闪电通道内NII离子的密度最大，并且大多数处于n＝3的激发态。     

新疆阿拉尔花岗岩MFC过程的微量元素综合效应

新疆阿拉尔花岗岩的微量元素比相关图显示了线性样点列与幂函数曲线形式的样点列相 复杂图型。该图型用简单混合或者单一结果分异模型都不能解释。本文建立了混合－结晶分异复合过程的微量元素综合效应模型。模型１：从初始混合线引起害虫函数曲线束形式的结晶分异线。特殊情况有结晶分异线简化为通过原点的直线束形式或者与初始混合线重合。     

合成磷灰石的去氟机理研究

用固相反应法和sol-gel法合成了不同类型的磷灰石（AP），并采用TEM、XRD、IR、BET比表面积法及静、动态吸附等方法研究了不同AP的比表面积、结晶度、晶胞参数、结晶尺寸、晶格缺陷度、Ca/P摩尔比和煅烧温度等与吸氟能力的关系，结果表明：结晶度高、晶粒大的AP有较小的吸氟量，属表面单分子层化学络合吸附机理；酸活化的AP有较大的吸氟量，属溶解-沉淀与沉淀物表面纳米尺寸效应吸附的复合去氟机理；具纳米尺寸的HAP在常温、常压、无二次污染、小于11mg/L的低含氟浓度废水中且不酸化情况下有较大吸氟量，属纳米尺寸效应吸附机理。     

唐古拉山冬克玛底冰川雪层中淋溶作用的初步研究

利用唐古拉山冬克玛底冰川雪坑和表层积雪样品的实测资料，初步探讨本区雪层中离子淋溶作用的特征，影响因素及其对冰芯记录的干扰。研究发现淋溶作用能够对数周至数月时间尺度的雪层记录产生“平滑”作用，但不会影响冰芯记录的长期变化趋势。     

河北平泉南梁岩体的岩石学研究

南梁岩体主要由斑状花岗岩、流纹斑岩、花斑岩及流纹质角砾熔岩组成。侵位时代为侏罗—白垩纪。岩石属钙碱性系列。斜长石的成分及有序度呈双峰型分布。条纹长石为交代成因。锆英石的标型特征表明岩石结晶作用经历了两个阶段。岩石结晶的温度在780°—1000℃之间。侵位深度<1km。南梁岩体是花岗—流纹岩型的次火山岩,可能是安山岩浆结晶分异的产物。     

Real-Time Observation on Water-Soluble Ions of PM_(2.5)in Beijing under the Influences of Different Air Masses in Summer

To further understand the variations of water-soluble ions in PM2.5 in Beijing,the authors observed their concentrations continuously and in high temporal resolution by the system for rapid collection of fine particles and ion chromatography(RCFP-IC) during 12–18 July 2010.These results combined with those of earlier backward trajectory research are used analyzed to determine the causes of concentration changes in water-soluble ions under the influences of two kinds of air masses in summer.The results indicate that concentrations of NO3-,SO42-,and NH4+ were influenced strongly by the continental air mass than by the marine air mass.Cl- and Na+ were not changed significantly.Because the sources of K+,Mg2+,and Ca2+ are mainly concentrated on land,their concentration levels were slightly higher under the control of continental air mass than that of the marine air mass.Variations of NO2- during the observation differed from those of other ions;its concentration was significantly higher under the influence of marine air mass.Moreover,the authors obtain the diurnal variations of eight water-soluble inorganic ions including NH4+,K+,Mg2+,Ca2+,Cl-,NO2-,NO3-,and SO42-.Diurnal variations of NH4+,NO3-,and Cl- showed single peak,which appeared before noon,while SO42- showed two peaks that appeared during rush hours.Those of Mg2+,Ca2+,and K+ showed single peak that appeared in the afternoon.That of NO2- showed with a peak appearing at sunrise and a valley appearing at sunset.     

临安地区强酸雨的特点

本文对1985年至1994年监测的强酸雨资料进行研究和分析，并与一般酸雨进行对比。结果表明，本地的一般酸雨出现较为频繁；强酸雨出现增多；四季中强酸雨频率各不相同，秋季最高，夏季最低；强酸雨的酸沉降量正在逐年增加；强酸雨的电导率较高，电导率和pH间呈现高度显著的负相关；强酸雨的降水量一般较小，并与pH间显现非常显著的正相关；强酸雨中各离子浓度均高于一般酸雨。