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1.
湘中奥陶纪沉积锰矿带位于湖南省安化县、桃江县、宁乡县境内,呈近EW向展布,矿带内锰矿以质量好而著称。该成矿带的成锰沉积盆地受控于加里东期张性断裂系统,为一断陷盆地。盆地内发育一组NW向同沉积断裂,形成了一系列断陷槽,控制了沉积岩相的分布。锰矿主要产于盆地中心亚相的黑色页岩夹碳酸锰矿微相内。据矿带中锰矿的地质和地球化学特征以及微量元素和碳、氧、锶同位素组成,笔者认为,该锰矿属于热水沉积成因。综合对比表明,该成矿带具有良好的成矿条件和值得注意的资源潜力,有可能发展为大型锰成矿带。  相似文献   
2.
利用1998年"大洋一号"调查船近海底作业所获的深拖海底电视和照相系统资料,对中国开辟区不利开采地形类型及其分布特征进行了研究,并对海底地形的坡度进行了计算,结果表明:(1)中国开辟区东、西两区海底的东向坡和西向坡是均衡分布的。东、西两区海底地形坡度的分布特征明显不同,东区海底地形坡度以0~15°为主,而西区坡度大于3°的地形则很少。坡度大于5°的地形主要分布于坡脚处,特别是坡度超过15°的地形总是出现在水深变化的转折点处。(2)研究区不利开采地形可分为坡度为5~15°和大于15°两种类型,东区地形坡度大于5°的不利开采地形比西区多14%,东区坡度大于15°的地形为3.6%,比西区(仅为1.4%)多,东、西两区都有少量坡度近90°的地形出现,并且这种地形在东区所占比率比西区大,说明东区断崖、陡坎和断裂沟槽比西区多,地形也更为复杂多变。  相似文献   
3.
通过对东北太平洋海域中国多金属结核开辟区沉积物间隙水中铜、锰、镍等微量元素的详细研究表明,锰主要受沉积环境的影响,其含量的变化范围在0.16~8.61μg/dm3之间;铜和镍则主要与表层海水的初级生产力有关,研究区内间隙水中铜和镍含量的变化范围分别为0.16~20.8和0.80~3.12μg/dm3,且这些元素在沉积物—水界面处均存在最大浓度梯度.利用“Fick扩散定律”计算表明,锰在研究区主要是从上覆海水向沉积物扩散,是沉积物中锰的主要来源之一;而铜和镍则是从沉积物向上覆海水扩散,是底层海水中铜和镍的主要来源。与表层海水中铜和镍向底层海水的输送通量计算结果相比,底层海水中铜和镍的含量主要受沉积物的控制.  相似文献   
4.
东太平洋多金属结核分布的二维趋势面分析   总被引:1,自引:0,他引:1  
对规则网的 469个测站的多金属结核丰度和 93个测站的 Mn、 Cu、 Co、 Ni元素进行趋势面分析 ,经 F检验 ,各变量的变异性显著 ,拟合度较低 ,表明多金属结核丰度及 Mn、Cu、Co、Ni金属元素的控制因素比较复杂。趋势面分析结果与相关分析结果一致 ,Mn、Cu、Ni元素有极相似的趋势特征 ,有两个轴向分布 ,一个为东西向轴 ,高值区在东部 ,另一个为北西向轴 ,高值区在北西部 ;结核丰度与 Co也有极相似的趋势特征 ,高值区在西部。应用逐次趋势面分析的结果将结核丰度的地质特征分解成各种简单控制因素的叠加 ,使对多金属结核的控矿因素、分布规律和物质来源的研究方法多样化  相似文献   
5.
根据1987、1988、1990年东北赤道太平洋CC区的3个航次多金属结核调查资料的统计分析,结果表明,CC区自西向东,从北向南,多金属结核丰度,覆盖率、形态、粒径和化学组分等具明显的区域分布规律,但在这一区域性分布背景上,结核的局部分布很复杂。  相似文献   
6.
Marine manganese nodules and crusts, when processed, yield tailings which may be utilized for environmental and economic benefit. The key to the reasonable and effective utilization of these tailings lies in making a systematic appraisal of their composition and properties. This article gives an introduction to the investigation of manganese tailings properties. The tailings have a high iron and/or manganese content, high surface area, high porosity, and fine grain size. Some tailings have a high rare earth element content which is valuable. They may also have high SO3, arsenic, and uranium contents which are harmful. Depending on the process used to produce the tailings, there will likely be some differences in chemical composition, mineral assemblages, surface area and adsorption capability, pore diameter and volume, density and pH. In assigning potentially beneficial applications for these tailings, these differences should be taken into account to optimize utilization.  相似文献   
7.
氧化锰矿物的生物成因及其性质的研究进展   总被引:5,自引:0,他引:5  
土壤中的氧化锰矿物是原生矿物风化和成土过程的产物,是最具反应活性的一类矿物,决定着环境中许多物质的形态、迁移和转化,在元素生物地球化学循环中起着重要的作用,其形成机制和环境效应备受关注。已有的研究表明,环境中氧化锰的形成与微生物作用紧密相关,微生物作用可使自然环境中的Mn(Ⅱ)氧化速率提高105倍。参与Mn(Ⅱ)氧化的微生物在环境中广泛存在,已知的典型锰氧化细菌分布在变形菌门、放线菌门或厚壁菌门,它们均通过胞外聚合物中的多铜氧化酶来催化氧化Mn(Ⅱ)。细菌氧化Mn(II)成Mn(Ⅳ)是酶催化的两个连续的快速单电子传递过程,Mn(Ⅲ)在溶液中以与酶结合的瞬时中间态出现。生物形成氧化锰的最初形态为层状锰矿物,与δ-MnO2或酸性水钠锰矿很类似,且结晶弱,粒径小,锰氧化度高,结构中的八面体空穴多,因而比化学形成的氧化锰具有更强的吸附、氧化等表面活性。环境中Mn(Ⅱ)微生物氧化及形成的Mn(Ⅲ)中间体与碳、氮、硫等生命元素的地球化学循环的关系令人关注。  相似文献   
8.
This is a 4-year longitudinal study to evaluate changes to the environment and exposure of young children associated with the introduction of methylcyclopentadienyl manganese tricarbonyl (MMT) into Australia in 2000. The cohort includes 57 females and 56 males; age range of 0.29 to 3.9 years. Samples are collected every 6 months from children in residences located at varying distances from major traffic thoroughfares in Sydney. Environmental samples: air, house and day care dustfall, soil, dust sweepings and gasoline. Samples from children: blood, urine, handwipes prior to and after playing outdoors, and a 6-day duplicate diet. All samples are analyzed for a suite of 20 elements using ICP-MS. Results are presented for the first three 6-month sampling periods for Pb and Mn. For dustfall accumulation, there was no significant change over the 3 sampling periods (time) for Pb or Mn, and a positive relationship between ‘traffic exposure' (traffic volume and proximity to the road) and Pb but not Mn. For handwipes, Pb and Mn in wipes taken from children after playing outdoors were usually significantly greater than for wipes taken prior to playing. There was no significant association between Pb or Mn in handwipes with traffic exposure. Dustfall accumulation was a significant predictor for Pb in the handwipes, and dust sweepings were a significant predictor of Mn in handwipes.  相似文献   
9.
Biological iron and manganese removal utilizing indigenous iron and manganese oxidizing bacteria (IRB hereafter) in groundwater can also be applied to arsenic removal according to our pilot-scale test. The arsenic removal probably occurred through sorption and complexation of arsenic to iron and manganese oxides formed by enzymic action of IRB. We investigated the chemical properties of iron and manganese oxides in IRB floc and the valence state of arsenic sorbed to the floc to clarify the mechanisms of the arsenic [especially As (Ⅲ)] removal. The floc samples were collected from two drinking water plants using IRB (Jyoyo and Yamatokoriyama, Japan), and our pilot - scale test site where arsenic and iron removal using IRB is under way (Mukoh, Japan). The Jyoyo and Yamatokoriyama IRB floc samples were subjected to As (Ⅲ) and As(Ⅴ) sorption experiments. The elemental composition of the floc samples was measured. XANES spectra were collected on As, Fe and Mn K-edges at synchrotron radiation facility Spring 8 (Hyogo, Japan). FT-IR and the X-ray diffraction spectra of the samples were also obtained. The IRB floc contained ca. 35 % Fe, 0.3%-3.5% Mn and 2%-6% P. The samples were highly amorphous and contained ferrihidrites and hydrated iron phosphate. According to XANES analyses of IRB, As associated with IRB was in +5 valence state when As (Ⅲ) (or As (Ⅴ)) was added in laboratory sorption test, Fe in +3 valence state, and Mn a mixture of+3 and +4 valence states. Small shift was observed in the XANES spectra of IRB on As K-edge as the equilibration time of the sorption experiment was increased. Gradual oxidation of a small amount of As (Ⅲ) associated with IRB or change in arsenic binding with sorption site were the probable mechanism.  相似文献   
10.
Abstract. Major and trace element contents are reported for Permian manganese ore and associated greenstone from the Ananai manganese deposit in the Northern Chichibu Belt, central Shikoku, Japan. The manganese deposit occurs between greenstone and red chert, or among red chert beds. Chemical compositions of manganese ore are characterized by enrichments in Mn, Ca, P, Co, Ni, Zn, Sr and Ba, and negative Ce and positive Eu anomalies relative to post-Archean average Australian Shale (PAAS). Geochemical features of the manganese ore are similar to those of modern submarine hydrother-mal manganese deposits from volcanic arc or hotspot setting. In addition, geochemical characteristics of the greenstone closely associated with the Ananai manganese deposit are analogous to those of with-in plate alkaline basalt (WPA). Consequently, the Ananai manganese deposit was most likely formed by hydrothermal activity related to hotspot volcanism in the Panthalassa Ocean during the Middle Permian. This is the first report documenting the terrestrially-exposed manganese deposit that was a submarine precipitate at hotspot.  相似文献   
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