高光谱影像数据预处理技术评价     

孙婷张立朝  唐汉松 《测绘科学与工程》2007,27(1):59-62

高光谱影像数据预处理是构建高效的影像数据库以及实现地理目标成分信息反演与地理目标识别的基础。本文从反射率演算、光谱微分技术以及高光谱影像数据的降维处理等三个方面对高光谱影像数据预处理进行了研究。实现了基于高光谱影像的反射率反演算法，针对高光谱遥感数据影像分辨率比较低的现状，提出了直方图均衡化、色调平衡、对比度调整等影像处理算法，并给出了实验结果。  相似文献   

低荧光防塌沥青及低荧光特效封堵防塌降滤失剂的研制与应用          下载免费PDF全文

李和良  陈艳霞 《探矿工程》2007,34(12):13-15

研发了一种具有优良防塌效果的低荧光钻井液用井壁稳定剂，提高石油沥青磺化度，解决降低产品荧光级别的新工艺，突破因荧光干扰测录井导致油储层被误判、漏判的关键技术，磺化反应后期，引入提高产品综合性能的特种材料进行交联反应。介绍了低荧光防塌沥青LF—TEX-1及低荧光特效封堵防塌降滤失剂FSL-1的关键技术原理和生产工艺流程，并对这两种处理剂的性能测试结果进行了分析。实际生产应用表明，他们具有明显的封堵、降失水功能。  相似文献   

宁夏主要气象灾害特征分析及防御对策   总被引：3，自引：0，他引：3  

李凤霞  马力文  李淑珍 《沙漠与绿洲气象(新疆气象)》2003,26(1):18-20

通过对1951－1996年出现的干旱、暴雨、洪水及雨涝、冰雹、风灾等主要气象灾害的特征和规律进行统计分析，总结得出：宁夏的气象灾害具有种类多，范围广，频次多，持续时间长，灾情严重，具有群发性和诱发性等特点。在此基础上提出了气象防灾减灾对策。  相似文献   

南海北部冷泉碳酸盐岩和石化微生物细菌及地质意义   总被引：22，自引：1，他引：22  

陈多福  黄永样  冯东  苏正  陈光谦 《矿物岩石地球化学通报》2005,24(3):185-189

通过对2002年广州海洋地质调查局在南海北部海域拖网采集的碳酸盐岩样品进行岩石、矿物、微量元素和同位素特征的研究，证实在南海水合物远景区发育有冷泉碳酸盐岩。冷泉碳酸盐岩形态类似于烟囱，主要由方解石、伊利石、石英、黄铁矿和一种未知的矿物组成。保存了很可能是石化的甲烷氧化和硫酸盐还原细菌。碳酸盐岩矿物的δ^13CPDB为-51.24‰～-51．757‰。碳酸盐岩矿物的页岩标准化稀土元素配分模式具无Ce和Eu异常、微弱的轻稀土亏损和中稀土富集特征，表明形成于还原的缺氧环境，显示了冷泉碳酸盐岩的特征，指示在南海北部水合物远景分布区内冷泉活动的近海底可能发育有水合物。  相似文献   

Experimental Study of Gold and Platinum Solubility in a Complex Fluid under Hydrothermal Conditions   总被引：2，自引：0，他引：2  

G. G. LIKHOIDOV  L. P. PLYUSNINA  J. A. SCHEKA  T. B. APHANAS EVA 《Resource Geology》2000,50(2):83-92

Abstract: The solubility of gold was studied in water and aqueous NaCl (1– 5 m) solutions under oxygen and sulfur buffered conditions between 300–500C at a constant pressure 1 kb. Two buffer assemblages HMP and PPM were used. Analysis of the scatter in measured values in log m_Au–m_NaCl–T frame fixed linear dependence between log m_Au and T at any studied iso‐pleth (m_NaCl) in the form of log m_Au = a. T(C) + b. Coefficients of the equation were calculated for water and NaCl (1, 3, 5 m) solutions. The maximum solubility characterizes the NaCl‐free system in the presence of HMP. In the case, Au solubility increases from (log m_Au) –6. 72 to –5. 04 at 300 and 500C, respectively. In the presence of PPM, maximum of Au solubility was obtained for the 5 mNaCl solution. In a similar manner solubility rises from –6. 54 to –5. 77 at 300 and 500C, accordingly. In studied f_O2/f_S2 area the behavior of Au solubility testified that: (i) – a composite interaction between chloride and hydrosulfide speciation of gold affects its total solubility; (ii) – in addition of NaCl up to about 1. 5 m the solubility decreases, more pronounced in the presence of HMP; (iii) – the contribution of chloride in total Au solubility is more for PPM despite of lower f_O2value, than for HMP. The solubility of platinum was studied in the Pt–Cl–S–H₂O system between 300 and 500C, 1 kb. PPM solid buffer controlled oxidation state, pH and sulfur activity of solutions (H₂O, 1 mNaCl and 0. 1 mHCl). Under the conditions, PtS precipitated from the solutions with increasing temperature and acidity. The PtS solubility in the 0. 1 m_HCl solutions lowers slightly in the range of 300–500C from –5. 30 to –5. 60 (in log m_Pt) that is typical to the hydrosulfide species. It was deduced that reducing media, regulated by the PPM assemblage, suppress activity of chloride species of Pt. More oxidizing conditions were modeled in runs using mixtures of Mn(II), Mn(III) and Mn(IV) oxides to buffer the aqueous‐chloride solutions between 300 and 500C, 1 kb. It was found that MnO tends to oxidize at T below 400C forming intermediate Mn‐hydroxides (β–MnOOH, Mn (OH)₂ and Mn₂(OH)₃Cl). These phases are metastable and transfer to Mn₃O₄ with increasing duration. Generation of the Mn‐hydroxides leads to a change of physical‐chemical parameters of the solutions, such as water activity, pH and Eh. The last results in abrupt increase in the noble metals dissolution. At stable existence of only Mn₃O₄, the solubility of both Pt and Au lowers to equilibrium values. Essential catalysis effect of Pt on intensity and rate of Mn(II) oxidation was found. The dominant role of chloride of Pt and Au was defined under most oxidized conditions, specified by Mn₂O₃–MnO₂ buffer. So at 400C, dissolved Au (log m_Au) increases from –4. 40 in water to –1. 00 in 0. 1 m_HCl, and ones of Pt (log m_Pt) from –4. 80 to –2. 90 accordingly. Thus, mixing of hydrosulfide and chloride solutions, as well as transformation of the systems to the stable state act upon total solubility of the noble metals.  相似文献   

Rio Tinto estuary (Spain): 5000 years of pollution   总被引：6，自引：0，他引：6  

R.A. Davis Jr.  A. T. Welty  J. Borrego  J. A. Morales  J. G. Pendon  J. G. Ryan 《Environmental Geology》2000,39(10):1107-1116

 Mining of massive sulfide deposits in southwestern Spain extending back to the Copper and Bronze Ages has resulted in the pollution of the Rio Tinto fluvial-estuarine complex, the site of Columbus' departure for the New World in 1492. Additional sources of potential pollution include the large industrial complex at Huelva near the lower portion of the estuary. Extensive analysis of surface sediment samples and cores has established that there are no geographic trends in the distribution of the pollutants, which include Cu, Fe, Pb, Zn, Ti, Ba, Cr, V and Co. These data have, however, demonstrated that tidal flux within the estuary carries phosphorus and perhaps other elements from the industrial complex at Huelva to the tidal limit of the system, several kilometers upstream from the discharge site. Radiometric analysis of short cores shows that sedimentation rates over at least the past couple of centuries have been about 0.3 cm/year. These data and that from a single deep core demonstrate that the estuary was polluted from mining activity long before the large-scale operations began in the late nineteenth century. Received: 3 May 1999 · Accepted: 18 October 1999  相似文献   

生物去除地下水中硫酸盐的实验研究   总被引：1，自引：0，他引：1  

张宏涛  翟辉 《地下水》2005,27(1):19-22

使用平皿夹层厌氧法分离得到纯化的硫酸盐还原菌,通过对比封口、敞口两种情况下细菌培养过程中产生的现象和细菌的生长曲线,表明SRB并非严格的厌氧菌,能耐受一定浓度的环境溶解氧.将该菌用于去除溶液中的SO42-,发现SRB在还原SO42-的过程中,随着SO42-去除率的增加,溶液的pH值会减小,而当SO42-去除率降低时,溶液的pH有增加的趋势;COD/SO42-比值对SO42-的去除率有很重要的影响,在封口情况下,COD/SO42-=0.75时SO42-的最大去除率约为48.60%,COD/SO42比值增加至2.5时,SO42-最大去除率可以达到89.72%,要达到SO42-高去除率,必须增加COD/SO42-比值.  相似文献   

Trace metals in suspended particulate matter and in sediment trap material from a permanently anoxic fjord — Framvaren, South Norway     

Jens M. Skei  Douglas H. Loring  Reijo T. T. Rantala 《Aquatic Geochemistry》1996,2(2):131-147

Geochemical studies of the trace metal concentrations in suspended particulate matter (SPM) and sediment trap material from a permanently anoxic fjord, Framvaren, South Norway in 1989 and 1993 indicate that extremely high concentrations of zinc (max = 183920 mg/kg), copper (max = 4130 mg/kg), lead (max = 2752 mg/kg), and cadmium (max= 8.1 mg/kg) sometimes (1993) occur in the SPM collected in the anoxic water layer. The highest concentrations of Zn occur just below the redoxcline at 22 m water depth (in 1993), and copper, lead and cadmium have maximum concentrations between 30 and 80 m depth, where the amount of total SPM is at a minimum (about 0.3 mg/L). On a mass per volume (g/L) basis, the maximum concentrations of Cd, Cu and Fe occur at the interface (21m) and those of Zn occur just below the redoxcline (22 m depth). The SPM and sediment trap data suggest that the metals are precipitated as sulfide minerals in the anoxic water. The presence of particulate sulfides was confirmed by SEM studies that show the occurrence of discrete metal (Cu, Fe, Pb, and Zn) sulfide particles in size from 10–20 m as well as framboidal pyrites (1–5 m in size). Higher levels of metal sulfides at intermediate depths rather than in the deep water of Framvaren (> 100 m), may be due to input of trace metals by water exchange over the sill in the upper part of the water column. In the deep water, less metal sulfide precipitation takes place due to depletion of trace metals, and the dilution of particulate metal concentrations by organic matter and by the chemogenic formation of calcite.  相似文献   

打桩对周围建筑物振动影响的研究与实例分析   总被引：5，自引：0，他引：5  

林建生  吴淑美  王源毅  叶传潜  林子健 《地震地磁观测与研究》1999,20(4):24-29

研究了打桩过程中土层质点振动速度的监测方法,打桩振动对周围建筑物影响程度的评价标准,并结合工程实例探讨了有关因素对检测结果的影响,及施工中应采取的相应减振措施。  相似文献   

Genesis of the Kamioka Skarn Deposits: An Important Role of Clinopyroxene Skarn and Graphite-bearing Limestone in Precipitating Sulfide Ore     

Yasuhiro KATO 《Resource Geology》1999,49(4):213-222

Abstract: A genetical relationship between skarn formation and mineralization is investigated for the Kamioka skarn deposits which are the largest Zn-Pb producer in Japan. In the Mozumi deposit, one of main deposits in the Kamioka mining area as well as Tochibora and Maruyama, clinopyroxene skarn was generally subjected to later replacement by garnet or magnetite–calcite–quartz during the Zn-Pb mineralization. The replacement of hedenbergitic clinopyroxene by andraditic garnet resulted in the formation of diopsidic clinopyroxene relicts. With the progress of replacement, the S/So value (So: an estimated area occupied by an original clinopyroxene grain in a thin section, S: a total area of relict clinopyroxene fragments) which is an index of the degree of replacement decreases from 0. 7 to 0. 1, and the hedenbergite mole percent of relict clinopyroxene decreases drastically from about 65 to less than 40. A close association of andraditic garnet and sphalerite suggests that heden-bergitic clinopyroxene skarn played an important role to reduce the relatively oxic ore-forming fluid enriched in Zn²⁺ and SO4^2– and to precipitate sphalerite from the fluid. Ferrous iron in the hedenbergitic clinopyroxene skarn was oxidized to form andraditic garnet. Besides this garnet formation, the mineral assemblage of magnetite–calcite–quartz replaced the clinopyroxene skarn at the time of mineralization. In both cases, the reduction of relatively oxic ore-forming fluid by hedenbergitic clinopy-roxene skarn at the later stage brought about the precipitation of sulfide minerals. In contrast, these types of later replacement are not found in the Tochibora deposit. Instead, graphite-bearing crystalline limestone and relatively fresh clinopyroxene skarn are common. Mineralized clinopyroxene skarn has high graphite carbon contents relative to barren one, suggesting that the amount of graphite in the skarn was an important controlling factor for mineralization. It is very likely that the graphite played a role of reducing agent during the mineralization in the Tochibora deposit.  相似文献