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1.
公共服务设施作为社区生活圈的核心内容,直接决定了社区生活圈的生活品质。对社区公共服务设施建设情况进行量化评价,并对设施建设的未来规划提供科学决策支持逐渐成为规划者和决策者的一大难题。本文通过ArcGIS工具对POI数据进行处理、统计和可视化,在总结他人社区生活圈量化评价方法的基础上,结合温州本地特色,搭建了一套社区生活圈公共服务设施评价模型。利用该模型可对各类社区进行综合评分和分级,并根据模型评分结果挖掘公共服务设施未来优化方向。此外,还实现了社区生活圈评分的动态计算与展示,为社区服务设施建设选址、路网建设与公共服务设施建设优先级评定等提供决策支持。既可帮助规划者和决策者快速建立对整个区域生活圈建设现状的量化认知,又可助力公共服务设施的优化配置,为社区生活圈公共服务品质评价与提升探寻全新的思路与方法。  相似文献   
2.
可持续发展中的公平与效率问题   总被引:3,自引:0,他引:3  
在传统增长方式中,公平与效率之间存在着巨大的冲突,由于可持续发展的出现,才第一次把两者纳入到可以相互补充、相互协调的框架之内,从而构成了整个社会得以生存与发展的必要张力。如何在公平的价值观念下效率,如何在有效的市场中保证公平,成为环境与发展问题相并列的当代经济理论、经济伦理思想以及可持续发展观的重要课题。  相似文献   
3.
为了明晰黏土矿物和盐分浓度在沉积过程中所起的作用及物理机制,选取高岭土、膨润土及两者组成的混合土进行粒径分析试验、沉积试验和Zeta电位测试。结果显示,盐分环境下高岭土和膨润土的平均粒径增大,部分黏粒组向粉粒组转化。高岭土在蒸馏水环境下和盐水环境下,最终都形成土-水的稳定分界面,但是絮凝稳定时间在盐分环境下更短。膨润土在蒸馏水环境下处于稳定的分散体系中,在盐水环境下迅速絮凝沉积。混合土在蒸馏水环境下,上部澄清层和下部沉淀层之间存在土颗粒的悬浮层,且该层的高度最终稳定;盐水环境下,混合土则迅速的发生土水分离。随着NaCl浓度增加,膨润土和高岭土的Zeta电位绝对值降低,因此胶粒组的絮凝行为对平均粒径产生影响,进而影响其沉积特性。  相似文献   
4.
天然气运移的气体同位素地球化学示踪   总被引:16,自引:0,他引:16  
本文通过鄂尔多斯等含油气盆地内岩石酸解烃、罐顶气和同源多产层天然气碳同位素组成的变化,从实例剖析出发,探讨了天然气运移时气体同位素组成的变化及其对天然气运移的示踪。天然气在通过沉积地层中孔隙系统和微裂隙运移时,天然气中的甲烷碳同位素会发生一定的分馏,而乙烷以上重烃碳同位素几乎不发生分馏;在天然气层所在深度,罐顶气甲烷碳同位素组成与天然气一致,在天然气层附近,罐顶气甲烷碳同位素则明显偏离了热演化趋势线;烃源岩酸解烃与其同源的天然气重烃碳同位素组成具有较好的一致性和可比性。由此,可利用气体组分碳同位素的上述变化特征,追索天然气的运移作用。  相似文献   
5.
Hydrogen sulfide (H2S) is known to catalyze thermochemical sulfate reduction (TSR) by hydrocarbons (HC), but the reaction mechanism remains unclear. To understand the mechanism of this catalytic reaction, a series of isothermal gold-tube hydrous pyrolysis experiments were conducted at 330 °C for 24 h under a constant confining pressure of 24.1 MPa. The reactants used were saturated HC (sulfur-free) and CaSO4 in the presence of variable H2S partial pressures at three different pH conditions. The experimental results showed that the in-situ pH of the aqueous solution (herein, in-situ pH refers to the calculated pH of aqueous solution under the experimental conditions) can significantly affect the rate of the TSR reaction. A substantial increase in the TSR reaction rate was recorded with a decrease in the in-situ pH value of the aqueous solution involved. A positive correlation between the rate of TSR and the initial partial pressure of H2S occurred under acidic conditions (at pH ∼3-3.5). However, sulfate reduction at pH ∼5.0 was undetectable even at high initial H2S concentrations. To investigate whether the reaction of H2S(aq) and occurs at pH ∼3, an additional series of isothermal hydrous pyrolysis experiments was conducted with CaSO4 and variable H2S partial pressures in the absence of HC at the same experimental temperature and pressure conditions. CaSO4 reduction was not measurable in the absence of paraffin even with high H2S pressure and acidic conditions. These experimental observations indicate that the formation of organosulfur intermediates from H2S reacting with hydrocarbons may play a significant role in sulfate reduction under our experimental conditions rather than the formation of elemental sulfur from H2S reacting with sulfate as has been suggested previously (Toland W. G. (1960) Oxidation of organic compounds with aqueous sulphate. J. Am. Chem. Soc.82, 1911-1916).Quantification of labile organosulfur compounds (LSC), such as thiols and sulfides, was performed on the products of the reaction of H2S and HC from a series of gold-tube non-isothermal hydrous pyrolysis experiments conducted at about pH 3 from 300 to 370 °C and a 0.1-°C/h heating rate. Incorporation of sulfur into HC resulted in an appreciable amount of thiol and sulfide formation. The rate of LSC formation positively correlated with the initial H2S pressure. Thus, we propose that the LSC produced from H2S reaction with HC are most likely the reactive intermediates for H2S initiation of sulfate reduction. We further propose a three-step reaction scheme of sulfate reduction by HC under reservoir conditions, and discuss the geological implications of our experimental findings with regard to the effect of formation water and oil chemistry, in particular LSC content.  相似文献   
6.
Wu  Sha  Wang  Qing  Wang  Xu  Guo  Ruixue  Zhang  Tongwei  Pan  Yongxin  Li  Feng  Li  Ying 《中国海洋湖沼学报》2021,39(6):2082-2096
Journal of Oceanology and Limnology - Based on analysis of gene structure of mamXY operon in Magnetospirillum gryphiswaldense strain MSR-1, we constructed a mamZ deletion mutant strain (ΔmamZ)...  相似文献   
7.
流体包裹体在油气地质地球化学中的应用   总被引:13,自引:3,他引:10  
流体包裹体研究是油气形成和成藏定量化研究的重要手段。本文总结了油气藏中流体包裹体的地质地球化学意义及其在石油、天然气研究中的应用,探讨了烃源岩和储层流体包裹体在确定源岩演化、沉积环境、有机母质类型、成熟度、油气运移充填期次等方面的应用,指出目前流体包裹体油气地球化学研究应关注的几个前沿方向:①在流体包裹体分析实验技术中,单个包裹体分析技术在油气地质定量化研究中具有重要的作用;②通过有机包裹体自然剖面与模拟实验对比研究烃类流体运移分馏,为建立油气成藏过程地球化学示踪指标提供基础参数;③通过储层中不同期次有机包裹体的化学组成、同位素组成、生物标志化合物与圈闭中已经聚集成藏的油气地球化学特征的对比研究,确定圈闭中油气的成因、来源和充填过程;④有机包裹体成烃作用研究为碳酸盐岩生烃和深层油气成因理论提供依据;这些方向的研究成果为深化油气理论、提高勘探水平具有重要意义。  相似文献   
8.
船载低频多波束测深声纳、侧扫声纳可以对深海海底地形地貌进行快速、高效、大面积探测,但其测量精度有限,难以满足深海科学考察、资源勘探开发对高精度海底地形地貌的需求。随着各类大深度水下移动载体(如深海拖体、水下机器人、遥控潜器和载人潜水器)的涌现,特别是各类耐高压测绘声纳的商业化,使大深度近海底精细地形地貌探测成为可能。首先分析了多波束测深声纳、侧扫声纳和测深侧扫声纳等3种测绘声纳的基本原理,然后分别介绍了各类测绘声纳的国内外典型商业化产品,并通过典型实例分析了其在大深度近海底精细测绘中的应用情况。  相似文献   
9.
In this study a series of CH4 adsorption experiments on clay-rich rocks were conducted at 35 °C, 50 °C and 65 °C and at CH4 pressure up to 15 MPa under dry conditions. The clay-dominated rock samples used are fresh samples from quarries and mines. Samples are individually dominated by montmorillonite, kaolinite, illite, chlorite, and interstratified illite/smectite. The experimental results show that clay mineral type greatly affects CH4 sorption capacity under the experimental conditions. In terms of relative CH4 sorption capacity: montmorillonite ? illite/smectite mixed layer > kaolinite > chlorite > illite. Physisorption is the dominant process for CH4 absorption on clay minerals, as a result, there is a linear correlation between CH4 sorption capacity and BET surface area in these clay-mineral dominated rocks. The abundance of micro-mesopores in the size range of a few to a few 10 s of nanometers in montmorillonite clay and illite–smectite interstratified clay results in large BET surface area values for these mineral species.  相似文献   
10.
The composition of gases trapped in olivine, orthopyroxene and clinopyroxene in Iherzolite xenoliths collected from different locations in eastern China has been measured by the vacuum stepped-heating mass spectrometry. These xenoliths are hosted in alkali basalts and considered as residues of partial melting of the upper mantle, and may contain evidence of mantle evolution. The results show that various kinds of fluid inclusions in Iherzolite xenoliths have been released at distinct times, which could be related to different stages of mantle evolution. In general, primitive fluids of the upper mantle (PFUM) beneath eastern China are dominated by H2, CO2 and CO, and are characterized by high contents of H2 and reduced gases. The compositions of PFUM are highly variable and related to tectonic settings. CO, CO2 and H2 are the main components of the PFUM beneath cratons; the PFUM in the mantle enriched in potassic metasomatism in the northern part of northeastern China has a high content of H2, while CO2 a  相似文献   
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