面向离散点的空间权重矩阵生成算法与实证研究

采用阈值法和k-近邻法度量空间上离散点间的空间邻接关系,针对不同的距离计算方式(欧式距离和曼哈顿距离)设计了面向离散点的空间权重矩阵生成算法,使用C#语言在计算机上实现。用该算法对收集的8 367个常州市地价样点构建了不同土地用途地价样点的空间权重矩阵,并计算出分用途的常州市城市地价空间自相关指数。     

硬X射线成像仪量能器测试系统的设计与实现

硬X射线成像仪(Hard X-ray Imager, HXI)是先进天基太阳天文台(Advanced Space-based Solar Observatory, ASO-S)的3大载荷之一, 其中量能器作为其重要组成部分, 承担着观测30--200keV能段的太阳硬X射线的任务. 在卫星发射之前, 需要开展大量的测试工作, 以确保HXI量能器的各项功能和性能满足设计需求. HXI量能器通道数众多, 内含99个溴化镧探测器, 分别由8块相同的前端电子学板控制. 除了对各个通道的性能进行测试外, 地检系统还需模拟量能器在轨面对不同太阳活动时的运行情况, 对量能器进行全面完备的测试. 此外, 地检系统还需足够稳定, 能满足量能器在单机测试、环境试验、热真空与振动等多个不同测试项目的长时间测试需求. 为此, 设计了地检板与上位机软件, 结合放射源、直流电源、高压模块等组成一套HXI量能器的地检系统, 对8块前端电子学板实现同步配置与管理, 能高效完成指令发送与数据接收, 满足量能器最大数据输出带宽400Mbps的需求. 利用该系统, 在地面完成了HXI量能器的功能、性能验证, 获得了量能器的线性、死时间、能量分辨率等各项性能指标, 为HXI量能器的在轨高性能运行提供了保障.     

海南岛4—9月短时强降水的天气型和环境参数特征

利用海南岛加密自动站逐小时降水资料、ERA5再分析资料,对海南岛短时强降水日环流配置进行了天气学分型,并进一步探讨了各天气型下海南岛短时强降水的时空分布、环流形势和关键环境参数特征。结果表明：(1)海南岛短时强降水有明显的日变化特征,呈单峰型,主要出现在15:00—19:00。(2)海南岛短时强降水的天气型主要有南海低压槽、华南沿海槽、西南低压槽和冷锋型。(3)南海低压槽、华南沿海槽、西南低压槽和冷锋型短时强降水分别占37%,31%,16%和16%。南海低压槽和华南沿海槽型主要出现在7、8和9月;西南低压槽型除9月外,其余各月份均可能出现;冷锋型绝大多数出现在4、5月。(4)南海低压槽和华南沿海槽型整层湿度条件都较好,不稳定能量较大,垂直风切变较弱。西南低压槽型不稳定能量较大,湿度条件一般,垂直风切变较弱。冷锋型存在明显的上干下湿特征,垂直风切变最大,0～6 km风速差75%分位大于10 m/s,不稳定能量最小。     

Fitting of magnetic measurements of Swarm satellites based on 3D surface spline model

This study utilizes the 62208000 Swarm satellite data to establish a high-precision main magnetic field at the height of the satellites in China and its adjacen...     

辽宁省霾天气季节变化特征及其主导因子分析

利用辽宁省51个地面气象观测站的能见度、均一化相对湿度和天气现象资料,采用最优距离法和固定比例法对能见度资料进行一致性处理,重建了1961—2020年的辽宁省逐日霾资料,并利用该资料对辽宁省年和四季霾日时空变化特征和主导因子进行分析。结果表明,1961—2020年辽宁省平均年霾日呈显著增加趋势[2.1 d·(10 a)^-1],但2015年以来霾日显著减少;空间上,年和四季霾日呈现一致的分布特征,均存在1个高值中心(沈阳)和2个副高值中心(北票和锦州),年平均霾日分别为139、52、46 d,辽东和辽西山区为霾日低发区,年平均霾日在20 d以内。风向和风速是霾日形成的重要气象因子,西南偏南风增加带来的暖湿气流对春季、夏季和秋季霾日的形成贡献较大,北风的减少则对冬季霾日的形成贡献较大。霾发生时辽宁省春季、夏季和秋季发生西南偏南风的频率分别由11.4%、12.1%和8.0%增加至15.8%、19.8%和13.5%,冬季则表现为北风发生频率的减少和静风发生频率的增加;霾发生时四季风速均较平均状况偏小,说明小风有利于霾的形成。辽宁省霾长期演变受到污染物排放、风力因子和环境政...     

The role of metal sulfates in thermochemical sulfate reduction (TSR) of hydrocarbons: Insight from the yields and stable carbon isotopes of gas products

The mechanism of thermochemical sulfate reduction (TSR) was investigated by separately heating n-C₂₄ with three different sulfates (CaSO₄, Na₂SO₄, MgSO₄) in sealed gold tubes at 420 °C and measuring the stable carbon isotope values of hydrocarbon (C₁-C₅) and non-hydrocarbon (CO₂) products. Extensive TSR was observed with the MgSO₄ reactant as reflected by increasing concentrations of H₂S, ¹³C depleted CO₂ and relatively low concentrations of H₂ (compared to the control). H₂S yields were already very high at the first monitoring time (12 h) when the temperature had just reached 420 °C, suggesting that TSR had commenced well prior to this temperature. Only trace amounts of n-C₂₄ and secondary C₃-C₅ alkanes were detected at 12 h, reflecting the efficient TSR utilization of the reactant and lower molecular weight alkane products. Ethane levels were still relatively high at 12 h, but declined thereafter as it was subject to TSR in the absence of higher molecular weight alkanes which had already been utilized. Methane yields were consistently high throughout the 48 h MgSO₄ treatment. The temporal decrease in the concentrations of alkanes available for TSR may also contribute to the sharp enhancement of CO₂ after 36 h. Absence or dampening of the molecular and isotopic trends of MgSO₄ TSR was observed with Na₂SO₄ and CaSO₄ respectively, directly reflecting the levels of TSR reached using these sulfate treatments.For all treatments, the δ¹³C values of C_1-5n-alkanes showed an increase with both molecular weight and treatment time. MgSO₄ TSR led to a 5-10‰ increase in the δ¹³C values of the C₁-C₅ hydrocarbons and a 20‰ decrease in the δ¹³C value of CO₂. The significant ¹³C depletion of the CO₂ may be due to co-production of ¹³C enriched MgCO₃, although this remains unproven as the δ¹³C of MgCO₃ was not measured. The difference in the δ¹³C values of ethane and propane (Δδ¹³C_EP) increased in magnitude with the degree of TSR, and this trend could be used to help evaluate the occurrence and extent of TSR in subsurface gas reservoirs.     

Geology, geochemistry, and age of volcanites of the Tunguda Volcanic Formation: The problem of the Archean-Proterozoic boundary in North Karelia

The geological, geochemical, and isotopic-geochronological data obtained for Sumian moderate-basic metavolcanites of Shombozero and Lekhta structures of the Panayarvi-Vygozero belt shows that the Tunguda Formation is confined to the Paleoproterozoic structural and material complex. This formation is represented by the complex of weakly differentiated andesitobasalts and andesites of calc-alkaline series with higher contents of MgO and moderate contents of Al₂O₃ and rare earth elements. The rocks of the Tunguda Formation are different from the Late Archean basic rocks of the Hiziyarvi Formation represented mainly by tholeiitic basalts with low REE contents and undifferentiated spectrum of REE distribution. The age of volcanites of the Tunguda Formation was determined to be 2439 ± 21 Ma. The xenogenic zircons from metaandesites of the Tunguda Formation have Neoarchean age according to the ²⁰⁷Pb/²⁰⁶Pb ratio (from 2536 ± 4 to 2825 ± 7 Ma). The Neoarchean zircons, a negative value of ?_Nd (?3.8), and indicative geochemical parameters are evidence that the crustal component took part in formation of the protolith of the studied rocks.