Modelling of the vertical fluxes of nitric acid,ammonia, and ammonium nitrate

Results from numerical investigations regarding the exchange of HNO₃, NH₃, and NH₄NO₃ between the atmosphere and the biosphere are presented. The investigations were performed with a modified inferential method which is based on the generally accepted micrometeorological ideas of the transfer of momentum, sensible heat and matter near the Earth's surface and the chemical reactions among these nitrogen compounds. This modified inferential method calculates the micrometeorological quantities (such as the friction velocity and the fluxes of sensible and latent heat), the height-invariant fluxes of the composed chemically conservative trace species with group concentrationsc ₁=[HNO₃]+[NH₄NO₃] (total nitrate),c ₂=[NH₃]+[NH₄NO₃] (total ammonia), andc ₃=[HNO₃]-[NH₃] as well as the fluxes of the individual nitrogen compounds. The parameterization of the fluxes is based on the flux-gradient relationships in the turbulent region of the atmospheric surface layer. The modified inferential method requires only the data of wind velocity, temperature, humidity and concentrations (HNO₃, NH₃, and NH₄NO₃) measured at a reference height by stations of a monitoring network.     

On the pH-dependent formation constants of iron(III)-sulfur(IV) transient complexes

An experimental study is described of Fe(III)-S(IV) formation constants measured as a function of pH (1–3), ionic strength (0.2–0.5 M) and [Fe(III)] _T (2.5–5.0×10^–4 M) using a continuous-flow spectrophotometric technique to make observations 160 ms after mixing. Preliminary experiments using pulse-accelerated-flow (PAF) spectrophotometry to measure rate constants on a microsecond timescale are also described. The conditional formation constant at 25 °C can be modeled with the following equation: {ie307-1} where {ie307-2}K ₇ andK ₈ can be interpreted as intrinsic constants for the coordination of HSO ₃ ^– by FeOH²⁺ and Fe³⁺, respectively, but until further evidence is obtained they should be regarded as fitting constants. PAF spectrophotometry showed that the initial reaction of Fe(III) with S(IV) (pH 2.0) is characterized by a second-order rate constant of 4×10⁶ M^–1 s^–1 which is comparable to rate of reaction of FeOH²⁺ with SO ₄ ^2– . However, the PAF results should be regarded as preliminary since unexpected features in the initial data indicate that the reaction may be more complex than expected.     

河北省唐山地区丰台—野鸡坨断裂第四纪活动性——来自14C和磁性地层年代学的证据

丰台—野鸡坨断裂为唐山地区主要断裂之一，西侧为鸦鸿桥凹陷，东侧为唐山凸起，断裂两侧第四系厚度之差巨大。本文依据该断层两侧钻孔对其第四纪以来活动性进行初步的探讨。通过对丰台—野鸡坨断裂上下两盘PZK14和PZK20孔磁性地层学研究，并结合钻孔岩石地层，及浅部光释光和¹⁴C测年结果，建立第四纪地层格架。结果表明：两孔底部“泥包砾”为新近纪沉积；PZK14孔下更新统底界埋深为387 m，中更新统底界埋深为114 m，上更新统底界埋深为71 m，全新统底界埋深为6 m；PZK20孔下更新统底界埋深为155 m，中更新统底界埋深为73 m，上更新统底界为36 m，无全新世地层。丰台—野鸡坨断裂活动在早更新世时表现为逐渐增强的特点，活动速率由早期的5.4 cm/ka增加到13.9 cm/ka。中更新世断裂活动基本处于停滞状态，活动速率为1.0 cm/ka。晚更新世以后，断裂重新活动，且更加剧烈，活动速率达到了54.5 cm/ka。     

Chrysophyte stomatocyst taxonomy — classification of snowflakes?

The utility of classifying chrysophyte stomatocysts by their characteristic honeycomb and ridge patterns is questioned, because a strikingly similar expanding pattern appears on the surface of ionized polymer gels during osmotical swelling as a result of simple physical forces. The rapid accumulation of silicate into a spherical cyst inside a chrysophyte cell appears to be as a physical process sufficiently similar to result in an analogous pattern in microscopic scale. Chrysophyte stomatocysts that possess honeycomb or ridge patterns could be regarded as frozen moments of the pattern evolution during the silicate gel phase. As a consequence, such structures should have little taxonomical value.     

The effect of acid deposition on base cation cycling in a karstic-forested catchment： Evidence from strontium isotopes

Bedrock weathering and atmospheric deposition are the two primary sources of base cations （K^＋, Na^＋, Ca^2＋ and Mg^2＋） to forest ecosystems. Therefore, the key problem is to understand the relative inputs from these two sources and the cycling in the ecosystem. This study focuses on the effects of acid deposition on cation cycling in a small-forested karstic catchment in Guizhou Province. Sr isotope ratios were used as a tracer for understanding the transport process between the different cation pools： rock, soil, surface water, atmospheric deposition and plant. The samples of wet deposition, total deposition, throughfall, surface and ground waters, vegetation, and soil were monthly collected. The exchangeable Sr^2＋ and Ca^2＋ in soil samples were extracted by using 1 M ammonium acetate. The leaf-tissue samples were ashed at 550℃, and the residue was digested in ultrapure HClO4 and HNO3. All water samples were filtrated through 0.45 μm aperture filter paper. Base cation concentrations and Sr isotopic composition were analyzed for all the samples. The results show that acid deposition （average pH 4.9） frequently occurred in the studied region. Cation abundance follows an increasing manner from rainwater, throughfall, to surface water or ground water samples, suggesting that acid deposition at first eiuviates Ca^2＋ , Mg^2＋ and Sr^2＋ from leaf, then the exchangeable cations from soil, and at last cations accumulate in surface water or ground water.     

湿地生态系统碳循环过程及碳动态模型

从地上、地下有机物质生产对湿地碳输入的贡献,湿地土壤碳库以及土地利用变化对湿地土壤碳库和碳排放的影响,甲烷排放和可溶性有机碳输出以及影响因子,湿地生态系统碳循环动态模型4个方面对湿地生态系统碳循环国内外研究进展和研究成果进行综述、分析,提出了我国亚热带区域天然湿地碳循环研究的主要热点和方向:⑴沿海湿地碳库估算及土地利用转化对土壤碳库和温室气体排放的影响;⑵酸沉降对于我国东南沿海低纬度地区湿地甲烷排放的影响;⑶沿海湿地生态系统碳循环动态模型的应用与开发;⑷湿地系统可溶性有机碳的输出机理探讨.     

Lake Sediment Core Records of Sulphur Accumulation and Sulphur Isotopic Composition in Central Ontario, Canada Lakes

Stable isotopic compositions and concentrations of total sedimentary sulphur (S) were determined in cores from 6 lakes in the acid-sensitive Muskoka-Haliburton region of south-central Ontario. The isotopic composition of S in deep sediment (> ~ 20 cm) was approximately constant in all lakes, and indicated a pre-industrial δ ³⁴S value between +4.0 and +5.3‰, which is similar to current bulk deposition. Similarly, total S concentrations in deep sediment were relatively low (1.9–5 mg S g⁻¹ dwt) and approximately constant with depth within cores. All lakes exhibited up-core increases in total S and decreases in δ ³⁴S at a depth corresponding to the beginning of industrialization in the Great Lakes region ( ~ 1900), resulting in a generally reciprocal depth pattern between total S concentration and δ ³⁴S ratios. While initial shifts in total S and δ ³⁴S were likely due to enhanced SO₄ reduction of newly available anthropogenic SO₄, both the magnitude and pattern of up-core S enrichment and shifts in δ ³⁴S varied greatly among lakes, and did not match changes in S deposition post 1900. Differences between lakes in total S and δ ³⁴S were not related to any single hydrologic (e.g., residence time) or physical (e.g., catchment-area-to-lake area ratio) lake characteristic. This work indicates that sediment cores do not provide consistent records of changes in post-industrial S deposition in this region, likely due to redox-related mobility of S in upper sediment.     

岩石、土壤样品中210Po测定方法的研究

研究了以铜箔为镀片时,自沉积总α计数法定量测定岩石、土壤样品中210Po的最佳制源环境、同位素的干扰和去除、共存元素的允许量以及适宜的溶(熔)矿方法,同时研究了银、铜两种镀片的区别。试验发现,当盐酸浓度为2.0mol/L,恒温80℃,振荡频率为180次/min、振程20mm时,制源2.0h,210Po自镀回收率在99.6%～100.4%之间,210Po加入量与α净计数率线性相关系数为0.9999。放置衰变法可以消除212Bi和218Po等短半衰期核素对210Po测量产生的影响,Vc存在时其它共存元素不干扰测定。方法配合HNO3HFHClO4溶矿(对复杂试样酸溶后的不溶渣,再进行碱熔),全程回收率为99.5%～100.4%。     

江西彭山锡多金属矿田地质地球化学特征研究

彭山锡多金属矿田位于长江中下游的九瑞地区，是近年来发现的一个以富锡、铅、锌矿产为主的大型矿田。以黑云母二长花岗岩与二云母碱长化岗岩组成的彭山隐伏岩体为中心，各类金属矿床呈“晕圈式”分布。矿床的形成分为2个成矿期共7个阶段，通过对彭山岩体、典型矿床及围岩中的硫同位素、铅同位素、包裹体及稀土资料进行分析，反映出燕山晚期钙碱性花岗岩体的缦位与多金属矿床的形成有着密切的联系，岩浆活动为本区提供了大量的成矿物质。