An equal area conversion model for rasterization of vector polygons

Vector-raster conversion is one of the classic research topics in the field of Geographical Information Systems (GIS). The algorithms commonly used in GIS are devoted to maintaining the vector polygons' shape characteristics, but neglect the gain and loss of a polygon's area, which is another important attribute. This paper proposes an equal-area conversion model based on an area compensation optimization principle. According to the topological relationship among polygons and boundary grids, a neighborhood compensation principle was adopted to assign the attributes of boundary grids and a global optimization algorithm was developed to minimize area distortion in the whole data set. Two experiments were designed and the results indicated that this algorithm not only guaranteed the area error is as small as possible, but also has the advantage as being adaptive to polygon shape and spatial structure.     

地图数字化数据坐标变换的相关性分析

将用于求定地图数字化坐标转换参数的已知点的地面坐标和数字化坐标都当作观测值，用随有参数的条件平差求定转换参数，对采用4个已知点、9个已知点分别进行相似与仿射变换进行了分析，计算了格网点之间的相关系数，进一步分析了格网点间相关系数的分布规律，对转换后的坐标相关性进行了讨论。     

水溶性污染物在土壤中转化的原位实验方法

建立了一种研究水溶性污染物在土壤中运转化的原位实验方法，该方法已成功地应用于研究黄土中氨氮的运移转化规律，克服了土柱实验存在的破坏土壤结构及氧化还原电位发生变化等所引起的实验误差。     

海洋风暴形成的一种动力学机制

文中从观测统计学、瞬变涡动能量学和 MM5中尺度数值模拟角度 ,研究了海洋风暴 (爆发性气旋 )形成的气候特征及其可能的动力学机制 ,揭示了一幅爆发性发展的物理图像。结果表明 ,在冷季大气特别是日本以东洋面上大气特有的热力气候背景下 ,通过同海洋风暴过程相联系的涡动热通量 vθ的向极地输送 (- vθ· θm>0 ) ,将季节尺度的时间平均有效位能向瞬变涡旋时间尺度的涡动有效位能转换 ,是海洋风暴形成的主要动力机制。在该过程中转换来的具有最大贡献的涡动有效位能 ,连同具有次大贡献的积云加热制造的涡动有效位能(q3 )一起 ,通过暖异常区 (α >0 )暖湿空气上升运动 (-ω >0 )的斜压转换 (-ωα) ,促使涡动动能增长。同时 ,补充的涡动有效位能又加强了暖异常区的暖湿空气上升运动 ,进而产生积云对流活动及其潜热释放的正反馈过程 ,最终导致涡动动能急剧增长和海洋风暴的形成。海-气潜热输送的作用是在风暴形成初期提供后来积云尺度对流活动及潜热释放的水汽潜力。研究还表明 ,海洋风暴主要发生在冷季月份 1 3 0°E以东的中高纬洋面上 ,这种对特定季节和特定海域的依赖性是大气和海洋气候背景的动力 /热力共同作用的结果     

临南地区石油运移方向与成藏期次研究

根据原油及油砂抽提物中含氮化合物分析、原油生物标志成熟度参数及储层流体包裹体烃类成分分析,研究了临南地区石油运移的方向、距离、成藏期次。结果表明临南油田仅有一期油气运聚成藏过程,属中新世末形成的成熟原油,4 甲基甾烷含量较高。曲堤油田存在两期油气运聚成藏过程,早期原油成熟度低,4 甲基甾烷含量低,运移距离较远,成藏后大部分散失 ;晚期充注的原油成熟度较高,4 甲基甾烷含量也较高,并保存至今。     

Element budgets of pine stands on lignite and pyrite containing mine soils

To analyze the development of pine ecosystems on lignite and pyrite containing mine soils, four pine stands with ages of 3–35 years were investigated in a chronosequence approach. Bulk precipitation, throughfall and soil solution in depths of 20, 40, 70 and 100 cm were studied over a three-year period to determine element fluxes in these forest ecosystems on extreme acidic and saline soils.Element budgets are controlled by the processes induced by pyrite oxidation such as intensive weathering of primary minerals, precipitation and leaching of secondary phases.Despite low water fluxes, element outputs can reach extraordinary high values due to very high concentrations in the soil solution. Although element outputs decrease drastically with stand age, respectively, site age, they exceed those of comparable pine stands on non-mine sites. Nitrogen release from the lignite fraction represents a special characteristic of the examined substrates. Nitrogen losses beneath the rooted zone can be 34 kg N ha⁻¹ yr⁻¹ in 100 cm depth. Element input and output in the examined ecosystems are far from balance. Closed cycling of nutrients seems to be recognizable in the case of potassium.     

Processing of oxidised nitrogen compounds by passage through winter-time orographic cloud

Four case studies are described, from a three-site field experiment in October/November 1991 using the Great Dun Fell flow-through reactor hill cap cloud in rural Northern England. Measurements of total odd-nitrogen nitrogen oxides (NO _y ) made on either side of the hill, before and after the air flowed through the cloud, showed that 10 to 50% of the NO _y , called NO _z , was neither NO nor NO₂. This NO _z failed to exhibit a diurnal variation and was often higher after passage through cloud than before. No evidence of conversion of NO _z to NO₃ ^- in cloud was found. A simple box model of gas-phase chemistry in air before it reached the cloud, including scavenging of NO₃ and N₂O₅ by aerosol of surface area proportional to the NO₂ mixing ratio, shows that NO₃ and N₂O₅ may build up in the boundary layer by night only if stable stratification insulates the air from emissions of NO. This may explain the lack of evidence for N₂O₅ forming NO₃ ^- in cloud under well-mixed conditions in 1991, in contrast with observations under stably stratified conditions during previous experiments when evidence of N₂O₅ was found. Inside the cloud, some variations in the calculated total atmospheric loading of HNO₂ and the cloud liquid water content were related to each other. Also, indications of conversion of NO _x to NO _z were found. To explain these observations, scavenging of NO _x and HNO₂ by cloud droplets and/or aqueous-phase oxidation of NO₂ ^- by nitrate radicals are considered. When cloud acidity was being produced by aqueous-phase oxidation of NO _x or SO₂, NO₃ ^- which had entered the cloud as aerosol particles was liberated as HNO₃ vapour. When no aqueous-phase production of acidity was occurring, the reverse, conversion of scavenged HNO₃ to particulate NO₃ ^-, was observed.     

Surface NO and NO2 mixing ratios measured between 30° N and 30° S in the Atlantic region

Surface NO and NO₂ mixing ratios were measured aboard the research vessel Polarstern during the mission ANT VII/1 from 24 September to 5 October 1988. The measurements were taken along the meridian at 30° W in the Atlantic region covering latitudes between 30° N and 30° S. The average mixing ratios were about 12 pptv NO/30 pptv NO₂ in the Northern Hemisphere and about 7 pptv NO/22 pptv NO₂ in the Southern. Elevated mixing ratios of 20 pptv NO/70 pptv NO₂ were found at 12° N (probably due to air masses originating from the surface of West Africa) and in the region of the ITCZ between 8° N and 5° N. Because of probable contamination by the ship, the measured mixing ratios mostly represent upper limits.     

里特曼标准矿物换算因数算法及评估

里特曼因数共有40个,实际上不敷使用,可运用里特曼稳定矿物组成原理来计算矿物换算因数,同理,还可计算出火成岩岩石密度的近似值。增补两个矿物换算因数:高岭石1.02;硬石膏1.19。     

Assessment of the Uncertainties in the NO2 and O3 Measurements by Visible Spectrometers

The column amounts of nitrogen dioxide (NO2) and ozone (O3) were measured using a visible spectrometer based on the twilight zenith-sky technique at two observatories located at similar latitudes in the northern part of Japan separated by a distance of 150 km. The measurements began in April 1991 at the Moshiri Observatory (44.4°N, 142.3°E) and in April 1994 at the Rikubetsu Observatory (43.5°N, 143.8°E). Since weather conditions and the possible influence from tropospheric pollution were not always identical at these two observatories, the overall accuracy of the measurements was studied comparing these data sets. The first year data obtained at a solar zenith angle of 90 degrees indicated that the NO2 slant column values at sunrise and sunset agreed within 0.36 and 0.54 × 1016 cm-2, respectively, corresponding to 5 % (June) and to 12 % (December) of the columns. The O3 values agreed within 0.76 × 1019 cm-2, corresponding to 4 % (March) 6 % (August) of the columns, although a part of the difference was systematic. The O3 column amounts were also compared to those obtained by the Dobson spectrometer at Sapporo (43.5°N, 143.8°E), whose latitude is similar to these observatories. When an air mass factor of 17.5 was used, the two-year Moshiri vertical column values agreed with the Dobson direct sun values to within 15 Dobson Units, or 3 6 % of the column. The difference between the two values was found to be due partly to the change in the air mass factor caused by seasonal and day-to-day changes in the shape of the O3 vertical profiles. These results confirm the reliability of the NO2 and O3 measurements by visible spectrometers at these sites for the Network for the Detection of Stratospheric Change (NDSC).