酒泉东盆地地下水“三氮”分布特征及健康风险分析

为探讨河西走廊地下水“三氮”的污染现状和个人健康风险。本文以酒泉东盆地为例,通过数据统计、空间分布趋势、污染源和影响因素分析的手段,从“三氮”分布、迁移和影响因素及其健康风险评价进行研究。结果表明：在其独特的地形地貌、氧化还原环境、包气带和含水层岩性、潜水的埋深、酸碱环境和地下径流条件等自然因素以及生态环境的破坏和城市化的发展等人为因素影响下,研究区地下水“三氮”总体含量较低,污染相对较轻,仅有一处NO₃^--N含量超过标准限值;区域分布上,“三氮”含量具有明显的北高南低的规律,NO₃^--N和NO₂^--N含量东、西两侧高,中间低,NH₄⁺-N含量由西北向东南逐渐减少。“三氮”个人年健康风险的整体分布趋势基本一致,由西部人口密集区域向东部人口非密集区域逐渐递减。     

Tolerance,oxygen consumption and ammonia excretion of Ophiopholis sarsii vadicola in different temperatures and salinities

There are more than 2000 species of brittle stars in the world. For most of them, many scientific questions including basic characteristics of eco-physiology are still unknown. In the present study, Ophiopholis sarsii vadicola acclimated at 15℃, salinity 31, were assessed for temperature and salinity tolerance. Its oxygen consumption and ammonia excretion were studied at different temperatures(5, 10, 15, 20, 25℃) and salinities(25, 30, 35). O. sarsii vadicola could tolerate 0–24℃ and no brittle star was dead in the salinity range of 19–48 in the experimental situation. Two-way ANOVA showed that the oxygen consumption and ammonia excretion normalized with both dry mass and wet mass, Q10, which is used to describe the temperature sensitivity of respiration, and moisture content were significantly affected by temperature and salinity, and the combined effects of the two factors were significant. Stepwise multiple regression analysis revealed that logarithmic oxygen consumption and ammonia excretion showed a significant positive relationship with logarithmic temperature and salinity. The logarithmic moisture content of the brittle stars showed an inverse relationship with logarithmic salinity, but a positive relationship with logarithmic temperature. This suggests that the tolerance of temperature and salinity of brittle stars is closely related to their living environment, and that the effects of temperature on oxygen consumption are more significant at higher salinity, and that the ammonia excretion is less affected by salinity at lower temperatures.     

微型生态系统中鲢、鳙下行影响的实验研究——2.营养物水平

鲢、鳙放养使微型生态系统的水柱氮、磷浓度和磷的分布发生了明显的变化。至实验结束时,各实验组的水柱颗粒磷、总磷和氨氮浓度都比对照组高,而正磷酸盐浓度和沉积物磷的量均低于对照组。这种变化以鳙单养系统为最大,其次是鲢、鳙混养系统,鲢单养系统的变化最小。微型生态系统中正磷酸盐浓度同浮游动、植物密度和初级生产力显著相关,氨氮浓度同所述变量之间的相关关系则多半与正磷酸盐相反。实验观测期间浮游植物密度与总磷浓度之间存在营养级联假说所预见的下行影响,实验结束时二者之间却有上行影响的趋向。根据实验观测结果认为,微型生态系统营养物(尤其是磷)水平的变动,主要是鲢、鳙的摄食改变了系统的群属结构和代谢强度的结果,同时反映了实验鱼对系统中营养物再生的影响。     

Pressurised Extraction Using Dilute Ammonia: A Simple Method for Determination of Iodine in Soil, Sediment and Biological Samples by Inductively Coupled Plasma-Mass Spectrometry

A simple sample treatment method for the accurate and precise determination of iodine in soil, sediment and biological samples by inductively coupled plasma-mass spectrometry (ICP-MS) is described. Iodine in samples was extracted in screw top PTFE-lined stainless steel bombs using a 10% v/v ammonia solution at 185 C for 18 hours (overnight), after which the extract was introduced into the ICP-MS for direct measurement. ¹²⁶Te was employed as the internal standard to compensate for matrix effects and instrument drift. The limit of detection (LOD, three times the standard deviation of the procedural blank solution, expressed as the concentration in the sample solution) was 0.003 ng ml-^-1. The limit of quantitation (LOQ, ten times the standard deviation of the procedural blank solution, expressed as the concentration in the solid samples, dilution factor DF = 100) was 0.01 μg g-^-1 (dry mass). The accuracy and precision of the method were demonstrated by analysing different Chinese geological certified reference materials (soils, stream sediments and a hair sample). The measured concentrations were in a good agreement with the certified values indicating that bias in the method was not significant. The precision (n = 10) for different concentrations ranged from 1.82% to 4.32% RSD. Comparison of the ammonia extraction procedure with a "sintering" method indicated that there was no significant difference in results obtained with the two methods for geological soil and stream sediment samples. However, for biological samples, such as hair, kelp, tea etc., the results obtained by the sintering method were far below those of the ammonia extraction method. The ammonia extraction has advantages, as it is simpler than the "sintering" method, and has a lower procedural blank, better detection limits and reproducibility. Due to the simplicity of the method, a high rate of sample throughput is possible.     

Measurements of Air Concentrations of SO2, NO2 and NH3 at Rural and Remote Sites in Asia

Sensitive diffusive samplers for concentration measurements in ambient airhave been used successfully in Sweden for several years. The samplers have theadvantage of being stable at room temperature before, as well as after,sampling, easy to handle, and cost-efficient. Furthermore, they do not requireelectricity or field calibration. In order to test their use in tropical andsubtropical environments and to obtain a preliminary set of data to validateatmospheric chemistry transport models in this part of the world, duplicatesamples were collected at 11 sites every second month during one year. Eightof the sites were background sites in Asia. It was not possible within theproject to compare the measured concentrations with other measurementtechniques. However, the reproducibility of the duplicates was satisfactoryover the whole measuring range (almost three orders of magnitude of theconcentration for SO₂) and reasonable agreement with modelcalculations was obtained at least for SO₂ andNH₃. Further testing of the measuring technique in tropicalareas is, however, warranted.     

Factors influencing ammonia volatilization from urea in soils of the shortgrass steppe

The effects of soil moisture, temperature, and humidity treatments on urea hydrolysis and NH₃ volatilization were assessed in the laboratory. Field studies were conducted to determine seasonal NH₃ losses from simulated urine patches applied to contrasting soils of a representative hillslope of the shortgrass steppe region in the North American Great Plains.Losses of NH₃–N were most influenced by soil moisture. The effects of temperature and humidity on total, or temporal, losses of NH₃ were dependent on soil moisture. Losses ranged from 18.5% under conditions of low-temperature/high-humidity/wet soil to 7.7% under conditions of high-temperature/low-humidity/dry soil. In contrast, urea hydrolysis was not affected by soil moisture.Losses of NH₃–N from simulated urine applied to field plots ranged from 1.5% on footslope soils in summer to 14.1% on backslope (midslope) soils in summer, whereas losses were 8.1% on back-slope soils in winter. Factors such as soil texture, microbial activity, and plant productivity along a toposequence had larger effects than climatic variables on variation in the volatile losses of NH₃–N from this grassland.This paper is a report on the work presented at the international symposium Influence of marine and terrestrial biosphere on the chemical composition of the atmosphere, held in Mainz, F.R.G., on 16–22 March 1986.     

Wet removal of highly soluble gases

Partition, not kinetics, ultimately determines the concentration of highly soluble gases in cloud droplets. Partition equations are formulated and applied to idealized air-mass thunderclouds and precipitating stratus. Contribution to aqueous concentrations from sub-cloud scavenging of highly soluble gases is estimated at between 10 and 20% under relatively unpolluted conditions. Data indicate that evaporation can produce enhancements in concentration of as much as a factor of 3. The calculations give large-scale mean coefficients of wet removal of highly soluble gases of about 2.8×10^-6 s^-1 (4-day residence time) for air-mass thunderclouds and precipitating stratus. Removal is so effective that the mean scale heights of these gases should be decreased to 2 km or less. The criterion of high solubility in this paper is that K ^H (Henry's Law coefficient) > 10⁵ mol l^-1 atm^-1. Gases that are effectively highly soluble include HCl, HNO₃, H₂SO₄, H₂O₂, NH₃ in acid droplets, SO₂ in oxidizing droplets (and probably some light amines and sulfonic acids), but not SO₂ in the absence of oxidants, nor HCHO. A variation of removal coefficient and scale height with solubility is presented. A comparison of atmospheric NH₃ concentrations deduced from rain NH₄ ⁺ and measured directly gives reasonable agreement.     

A three-dimensional model of the global ammonia cycle

Using a three-dimensional (3-D) transport model of the troposphere, we calculated the global distributions of ammonia (NH₃) and ammonium (NH ₄ ⁺ ), taking into account removal of NH₃ on acidic aerosols, in liquid water clouds and by reaction with OH. Our estimated global 10°×10° NH₃ emission inventory of 45 Tg N-NH₃ yr^– provides a reasonable agreement between calculated wet NH ₄ ⁺ deposition and measurements and of measured and modeled NH ₄ ⁺ in aerosols, although in Africa and Asia especially discrepancies exist.NH₃ emissions from natural continental ecosystems were calculated applying a canopy compensation point and oceanic NH₃ emissions were related to those of DMS (dimethylsulfide). In many regions of the earth, the pH found in rain and cloud water can be attributed to acidity derived from NO, SO₂ and DMS emissions and alkalinity from NH₃. In the remote lower troposphere, sulfate aerosols are calculated to be almost neutralized to ammonium sulfate (NH₄)₂SO₄, whereas in the middle and upper troposphere, according to our calculations, the aerosol should be more acidic, as a result of the oxidation of DMS and SO₂ throughout the troposphere and removal of NH₃ on acidic aerosols at lower heights. Although the removal of NH₃ by reaction with the OH radical is relatively slow, the intermediate NH₂ radical can provide a substantial annual N₂O source of 0.9 _–0.4 ^+0.9 Tg, thus contributing byca. 5% to estimated global N₂O production. The oxidation by OH of NH₃ from anthropogenic sources accounts for 10% of the estimated total anthropogenic sources of N₂O. This source was not accounted for in previous studies, and is mainly located in the tropics, which have high NH₃ and OH concentrations. Biomass burning plumes, containing high NO _x and NH₃ concentrations provide favourable conditions for gas phase N₂O production. This source is probably underestimated in this model study, due to the coarse resolution of the 3-D model, and the rather low biomass burning NH₃ and NO _x emissions adopted. The estimate depends heavily on poorly known concentrations of NH₃ (and NO _x ) in the tropics, and uncertainties in the rate constants of the reactions NH₂ + NO₂ N₂O + H₂O (R4), and NH₂ + O₃ NH₂O + O₂ (R7).     

Shock temperature in calcite (CaCO3) at 95-160 GPa

The temperatures induced in crystalline calcite (CaCO₃) upon planar shock compression (95-160 GPa) are reported from two-stage light gas gun experiments. Temperatures of 3300-5400 K are obtained by fitting six-channel optical pyrometer radiances in the 450-900 nm range to the Planck gray-body radiation law. Thermodynamic calculations demonstrate that these temperatures are some 400-1350 K lower than expected for vibronic excitations of the lattice with a 3R/mole-atom specific heat (R is gas constant). The temperature deficit along the Hugoniot is larger than that expected from only melting. In addition to melting, it appears likely that shock-induced decomposition of calcite occurs behind the shock front. We modeled disproportionation of calcite into CaO (solid) plus CO₂ (gas). For temperature calculations, specific heat at constant volume for 1 mole of CO₂ is taken to be 6.7R as compared to 9R in the solid state; whereas a mole of calcite and a mole of CaO have their solid state values 15R and 6R, respectively. Calculations suggest that the calcite decomposes to CaO and CO₂ at ∼110±10 GPa along the Hugoniot. Recent reanalysis of earlier VISAR measurements of particle velocity profiles [1] indicates that calcite shocked to 18 GPa undergoes disproportionation at much lower pressures upon isentropic expansion.     

大洋锰结核氨浸渣作为陶瓷原料的实验研究

通过研究大洋锰结核经氨浸工艺提取Co,Ni,Cu等有价金属后的粉末状固体残渣（氨浸渣）对石英-长石-高岭土3组分陶瓷体系烧结行为及制品性能的影响发现：3组分体系中添加不超过10％的氨浸渣,在1140℃烧结90min,烧结体的抗折强度大于65．9MPa,吸水率小于0．128％．达到JC／T665-1997规定的要求。氨浸渣的助熔效果明显,添加5％～10％即可降低3组分陶瓷烧结温度40℃～80℃,添加量过多（超过10％）会增加熔体相含量．易引起坯体过烧,不利于坯体致密化和烧成工艺控制。添加氨浸渣,烧结体呈灰白色一黄褐色,且烧结体颜色随氨浸渣含量增加而变深。研究认为,氨浸渣可以作为石英-长石-高岭土3组分陶瓷的助熔剂和色料。