1990年6月14日苏联斋桑湖7.3级地震和两次强余震前富蕴地震窗的异常及其预报

近年来,地震窗预报方法已在国内广为应用。富蕴地震窗系笔者在王泽皋、姜秀娥等人工作的基础上^[1-3],于1984年在全国地震预报清理攻关中建立,在1987-1988年全国地震预报实用化攻关中又得以进一步深化和完善^[4]。     

基于二阶局部纹理熵的边缘检测方法

针对传统的边缘检测方法将灰度变化较为平缓的区域误判为边缘的问题,提出了基于二阶局部纹理熵的边缘检测方法。利用了二阶局部纹理熵能表示局部区域灰度变化大小的性质,并采用灰度错位压缩法消除灰度值压缩造成的条纹现象。实验表明,本文提出的方法能有效地检测出各类边缘,解决了上述的误判问题;通过不同大小窗口的边缘检测效果比较,建议在采用基于二阶局部纹理熵的边缘检测方法时将窗口设置为3×3。     

The effects of slope shape and polyacrylamide application on runoff,erosion and nutrient loss from hillslopes under simulated rainfall

Natural hillslopes are mostly composed of complex slope shapes, which significantly affect soil erosion. However, existing studies have mainly focused on uniform slopes to simplify complex hillslopes, and the mechanisms responsible for the influence of slope shape on soil and nutrient losses are still not well understood, especially in the application of soil improvers to reduce soil loss. To investigate the effects of slope shape and polyacrylamide (PAM) application on runoff, soil erosion and nutrient loss, this study conducted artificial field rainfall experiments involving two PAM application rates and nine slope shapes. The results indicate that the average amount of soil loss from convex slopes was 1.5 and 1.3 times greater than that from concave and uniform slopes, respectively, and the average amount of ammonia nitrogen loss and phosphate loss increased by 24.0%–58.6%. Soil and nutrient losses increased as the convexity of the convex slopes increased. For runoff, there was little difference between concave and convex slopes, but the runoff amount for both slopes was greater than that for uniform slopes. After PAM application, the soil loss decreased by more than 90%, and the nutrient loss decreased by 28.2%–68.1%. The application of PAM was most effective in reducing soil erosion and nutrient loss from convex slopes, and it is recommended to appropriately increase the PAM application rate for convex slopes. A strong linear relationship between ammonia nitrogen and phosphate concentrations and sediment concentrations was found in the runoff on slopes with no PAM application. However, this linear relationship weakened for slopes with PAM application. The findings of this study may be valuable for optimizing nonpoint source pollution management in basins.     

Development of Synthetic Clinopyroxene Reference Materials for In Situ Lithium Isotope Measurement by LA-MC-ICP-MS

The isotopic composition of lithium (Li) in clinopyroxene (Cpx), determined via in situ micro-analysis, has been employed as a potential geochemical tool for studying various geological processes such as crust-mantle recycling, silicate weathering and fluid-rock interaction. To obtain precise and accurate Li isotopic compositions in Cpx by LA-MC-ICP-MS, synthetic Cpx matrix-matched reference materials (RMs) were prepared in this study. Six Cpx-matrix RMs were prepared by mixing metallic oxides with GSP-2 (granodiorite) or pure L-SVEC solution and melting them into glasses (GSP-2 + oxide; L-SVEC + oxide). Two representative synthetic glasses, CPXA01 and CPXB01, were subjected to a series of analyses to investigate the possible qualification of the RMs for in situ Li isotope measurement by LA-MC-ICP-MS, including elemental homogeneity analysis (elemental mapping analysis and spot analysis), Li isotopic homogeneity analysis and accurate Li isotopic determination. The applicability of the synthetic Cpx-matrix RMs was highlighted by comparing the δ⁷Li values of three natural Cpx calibrated against the synthetic Cpx-matrix RMs and other commonly used RMs with different matrices (NIST SRM 612, BCR-2G, GOR128-G, StHs6/80-G, KL2-G and T1-G), respectively. Additionally, CPXB01-05 RMs with the same matrix but different Li contents were prepared to explore the Li content mismatch effect, which is significant for accurate determination of in situ Li isotopic composition by LA-MC-ICP-MS. The results of the cross-calibration of Li isotopes in CPXA01 and CPXB01 suggested no obvious Li isotopic fractionation between the two types of glasses (GSP-2 + oxide; L-SVEC + oxide). Thus, the two methods of producing Cpx-matrix RMs are suitable for preparing the matrix-matched RMs for in situ microanalysis for Li isotopes.     

新疆哈密土屋铜矿床地质和地球化学特征

土屋铜矿床是我国近年来发现的特大型斑岩铜矿床,其独特矿床地质背景和矿床规模已经引起国内外地质学界和矿业界的广泛关注;本文详细叙述该矿床的地质背景,对矿床的地质、地球化学特征进行系统研究和总结,对矿床的成矿作用动力学过程进行探讨。研究表明,该矿床成矿物质具有深部来源特征,而岩浆在侵位过程中受到上地壳物质一定程度的混染;成矿流体以岩浆水为主,天水和岩浆水的混合仅为少量;石英流体包裹体均一温度较低,但盐度较高;含矿斑岩体是多次脉动式侵位的,成岩时代主要集中于早石炭世(367～358 Ma);成矿时代为晚于成岩时代(347.3±2.1 Ma～322.7±3 Ma)。     

Groundwater discharge to the Changjiang River, China, during the drought season of 2006: effects of the extreme drought and the impoundment of the Three Gorges Dam

Groundwater can play an important role in the compensation of runoff reduction due to extreme climate events such as droughts, as well as in response to anthropogenic actions such as the construction of a dam. The increase in ²²⁶Ra specific activity and the runoff from September to December in 2006 is used to estimate the total discharge of groundwater along the mid-lower reaches of the Changjiang River. The total groundwater discharge was found to account for 31% of the increased discharge between Yichang and Datong. The groundwater discharge to lakes (i.e. Dongting Lake) constituted the major contribution of groundwater discharge to the mid-lower reaches of the Changjiang River. More importantly, the second impounding operation of the Three Gorges Dam from 20 September to 27 October 2006 induced a water level decrease in surrounding lakes and rivers, which led to an additional groundwater discharge of 63.3?×?10⁸?m³, accounting for 85% of the total groundwater discharge in the same period. Taken together, these observations indicate that groundwater discharge along the mid-lower reaches plays an important role in maintaining stream flow in the drought season, especially in extreme drought years or in response to human activities.     

共存镉/铜对沉积物(生物膜)中主要组分吸附阿特拉津的影响

采用选择性萃取分离技术对沉积物(生物膜)中非残渣态组分(铁、锰氧化物和有机质)进行分离,研究阿特拉津(atrazine,AT)-Cd-Cu系中共存重金属对选择性萃取前后沉积物(生物膜)吸附AT的影响.研究结果表明:共存体系中,沉积物(生物膜)中铁氧化物对AT的吸附贡献最大,其次是有机质,而锰氧化物则抑制AT的吸附;共存镉促进了AT在沉积物(生物膜)原样及各非残渣态组分上的吸附,镉质量浓度为0.2 mg/L时,促进作用最显著,各组分对阿特拉津的吸附贡献增加了3.20%～32.31%(沉积物)和1.61%～17.10%(生物膜),但随镉质量浓度的增加,其促进作用减弱;共存铜抑制沉积物(生物膜)原样及铁氧化物、有机质对AT的吸附,铜质量浓度为75.0 mg/L时,其抑制作用最强,铁氧化物和有机质对阿特拉津的吸附贡献分别降低了29.21%、22.36%(沉积物)和9.46%、77.27%(生物膜),但同时减弱了锰氧化物对AT吸附的抑制作用,其吸附贡献分别提高了28.98%(沉积物)和17.46%(生物膜).