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261.
The Skaergaard liquid line of descent revisited 总被引:1,自引:0,他引:1
Peter Thy Charles E. Lesher Christian Tegner 《Contributions to Mineralogy and Petrology》2009,157(6):735-747
There is a fundamental conflict between the suggestion that the iron content of Skaergaard liquids increases during Fe–Ti
oxide fractionation and the observation that at the same time oxygen fugacity () drops by two log-units below the fayalite-magnetite-quartz oxygen buffer (FMQ). A new petrographic study of average Skaergaard
gabbros shows that the total modal content of Fe–Ti oxides is about 22% in the early LZc and markedly decreases to below 5%
in the UZc. Forward modeling based on these modal constraints, as well as experimental results on Skaergaard-related dikes,
predicts that fractionation of troctolitic LZa gabbros drives the derivative liquid towards a high-iron content. Strong iron
enrichment continues, together with a small decline in silica, during LZb crystallization due to the appearance of augite
as a fractionating phase. The fractionation of Fe–Ti oxides in the LZc initially suppresses iron enrichment and reverses the
silica trend to one of slight enrichment. However, continued evolution into the UZ produces liquids with maximum UZc FeO*
content of 23–25 wt.% and SiO2 content of 53 wt.% (FeO* is total iron as FeO). The maximum in FeO* is dependent on several factors of which the Fe–Ti oxide
mode has the strongest effect. The during crystallization of the LZc is widely thought to have been at, or slightly below, the fayalite-magnetite-quartz oxygen
buffer (FMQ). Under closed system evolution, incorporation of ferric iron into augite during formation of the LZb restricts
the increase in to about 0.1 log-units above FMQ (=0.1 ΔFMQ). Likewise, crystallization of the LZc through the UZa, involving Fe–Ti oxide
minerals, leads to a decline in of less than 0.1 ΔFMQ. Crystallization of the UZb-c gabbros results in oxidation to a maximum of 0.5 ΔFMQ. This behavior
can account for the iron-rich character of the UZ gabbros, as well as, the low modal content of Fe–Ti oxides. Thus, evolved
Skaergaard liquids are high in iron and contain a modest amount of SiO2. Our modeling result do not account for a strong drop in through the layered series. Such a drop would require an unacceptably high proportion of Fe–Ti oxides and high-magnetite
content in the fractionating assemblage.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
262.
We have investigated melting relations in the Fe–O–S ternary system in the pressure range of 15–27 GPa and 1873 K. Subsolidus
phase relations are Fe, Fe3S2, and FeO up to 17 GPa and Fe, Fe3S, and FeO above this pressure. The eutectic temperature slightly decreases from ambient pressure to 17 GPa, whereas increases
above this pressure. The eutectic temperature in this study is 100 K lower than that in the Fe–S binary system. The oxygen
content in the Fe–O–S eutectic liquid drops when the coexisting solid phases changes from FeS to Fe3S2. The cotectic lines in the ternary phase diagram lie close to the Fe–FeS binary axis. The isothermal sections indicate that
oxygen solubility in the Fe–O–S liquid increases with increasing temperature, and with increasing sulfur content. The solubility
of sulfur in the solid Fe has a maximum value at the eutectic temperature, and decreases with increasing temperature. Our
results could have important implications for formation and composition of the Martian core. 相似文献
263.
Huan-Xin Weng Ya-Chao Qin Xiang-Wei Sun Xun-Hong Chen Jing-Feng Chen 《Environmental Geology》2009,57(1):9-15
Laboratory culture experiments have been conducted to evaluate the effects of light intensity on the growth of Cryptomonas sp. (Cryptophyceae) and the discrepancy in absorption of iron and phosphorus under different light conditions. Results show
that there is an exponential correlation between algal growth rate and light intensity. The saturating and semi-saturating
light values for Cryptomonas sp. cells are 150 and 47 μmol photons m−2 s−1, respectively. More uptake of Fe, P, and other trace elements such as Zn, Mn, Co, and Mo is observed in the low light cultures,
although the algal growth rates are slow. The growth rate at 10 μmol photons m−2 s−1 is only 10% of that at 150 μmol photons m−2 s−1, whereas Fe and P uptake increases by 150 and 100%, respectively. These results suggest potential implications of differentiation
in absorption of iron and phosphorus at different light intensities for the occurrence of harmful algal blooms (HABs). The
mechanisms of light intensity regulating nutrient uptake as well as the occurrence of HABs are also discussed. 相似文献
264.
在土壤和沉积物的自然厌氧环境中,铁氧化物可被铁还原菌等微生物异化还原产生Fe(Ⅱ),形成的Fe(Ⅱ)/铁氧化物表面结合铁系统具有还原活性,可使有机污染物还原转化。综述了含卤和含硝基有机污染物的非生物还原转化过程和表面结合铁系统与有机污染物之间的界面反应机理,进而揭示了污染物在环境中的赋存状态和迁移转化规律;重点分析了影响该还原过程的因素,如铁氧化物类型、pH值、Fe(Ⅱ)与铁氧化物接触时间,以及过渡金属、腐殖酸等竞争因子对反应过程的影响。强化自然界中天然的Fe(Ⅱ)/铁氧化物表面结合铁系统在有机污染治理中的作用,在受污染环境修复领域具有广阔的应用前景。
[HT5H]关 键 词:[HT5K] 相似文献
265.
Yvonne Thompson Brian C. Sandefur A. D. Karathanasis Elisa D’Angelo 《Aquatic Geochemistry》2009,15(3):349-370
Redox potentials (Eh) were monitored bimonthly and porewater chemistry was analyzed seasonally at three slightly-acidic, high-elevation
Kentucky wetlands that differed in hydrology, parent materials, and vegetation. At all sites, Eh values were below 300 mV,
which indicated that reducing conditions persisted within the upper 90 cm and fluctuated mainly within the range of iron and
sulfate reduction. Significant relationships of Eh values with depth were observed only at the Martins Fork wetland, where
precipitation was the primary water source. The strongest and most stable reducing conditions, observed at the Kentenia site,
reflected consistently high water levels, which were sustained by ground water. The third wetland (Four Level) was distinguished
by irregular Eh fluctuations coinciding with strong seasonal ground-water upwelling. Although Fe3+ and SO4
2− were the primary terminal electron acceptors in all wetlands, porewater chemistry also varied significantly by season and
soil depth in response to piezometric water level fluctuations. Additional factors that influenced porewater chemistry included:
(1) the presence of limestone parent materials that affected porewater pH, Ca2+, and Mg2+; and (2) the prevalence of sphagnum moss or graminoid species that influenced dissolved organic carbon, CO2, and CH4. Results from this study indicated the diverse range and importance of multiple factors in controlling biogeochemical processes
and properties in small, high-elevation Appalachian wetlands. 相似文献
266.
The production of iron oxide during peridotite serpentinization: Influence of pyroxene 总被引:1,自引:0,他引:1
Ruifang Huang Chiou-Ting Lin Weidong Sun Xing Ding Wenhuan Zhan Jihao Zhu 《地学前缘(英文版)》2017,8(6):1311-1321
Serpentinization produces molecular hydrogen(H2)that can support communities of microorganisms in hydrothermal fields;H2 results from the oxidation of ferrous iron in olivine and pyroxene into ferric iron,and consequently iron oxide(magnetite or hematite)forms.However,the mechanisms that control H2 and iron oxide formation are poorly constrained.In this study,we performed serpentinization experiments at 311℃ and 3.0 kbar on olivine(with 5% pyroxene),orthopyroxene,and peridotite.The results show that serpentine and iron oxide formed when olivine and orthopyroxene individually reacted with a saline starting solution.Olivine-derived serpentine had a significantly lower FeO content(6.57±1.30 wt.%)than primary olivine(9.86 wt.%),whereas orthopyroxene-derived serpentine had a comparable FeO content(6.26±0.58 wt.%)to that of primary orthopyroxene(6.24 wt.%).In experiments on peridotite,olivine was replaced by serpentine and iron oxide.However,pyroxene transformed solely to serpentine.After 20 days,olivine-derived serpentine had a FeO content of 8.18±1.56 wt.%,which was significantly higher than that of serpentine produced in olivine-only experiments.By contrast,serpentine after orthopyroxene had a slightly higher FeO content(6.53±1.01 wt.%)than primary orthopyroxene.Clinopyroxene-derived serpentine contained a significantly higher FeO content than its parent mineral.After 120 days,the FeO content of olivine-derived serpentine decreased significantly(5.71±0.35 wt.%),whereas the FeO content of orthopyroxene-derived serpentine increased(6.85±0.63 wt.%)over the same period.This suggests that iron oxide preferentially formed after olivine serpentinization.Pyroxene in peridotite gained some Fe from olivine during the serpentinization process,which may have led to a decrease in iron oxide production.The correlation between FeO content and SiO_2 or AI_2 O_3 content in olivine-and orthopyroxene-derived serpentine indicates that aluminum and silica greatly control the production of iron oxide.Based on our results and data from natural serpentinites reported by other workers,we propose that aluminum may be more influential at the early stages of peridotite serpentinization when the production of iron oxide is very low,whereas silica may have a greater control on iron oxide production during the late stages instead. 相似文献
267.
南任铁矿床位于莱州-安丘铁成矿带西北部,对其矿床成因认识存在较多争议。矿区内地层广布,构造、岩浆岩不发育。铁矿体呈透镜状产于滹沱纪粉子山群小宋组的底部层位,无穿插或交代围岩现象;围岩蚀变以蛇纹石化、绿泥石化为主,愈近矿体矿化蚀变愈强。矿石矿物以磁铁矿为主,少量黄铁矿、黄铜矿;脉石矿物主要为蛇纹石、绿泥石。矿石的结构构造主要为浸染状构造,半自形—他形粒状结构。岩矿石稀土元素含量表明磁铁矿主要为火山深成岩浆结晶分异形成,部分与火山沉积作用有关;磁铁矿化学成分特征也反映了这一点,综合认为其成因可能属海相火山岩型之火山岩浆-热液和火山沉积复合类型。在此基础上,总结了莱州-安丘铁成矿带上不同成因铁矿床的分布规律,为今后该地区铁矿勘查指明了方向。 相似文献
268.
山东省东平-汶上铁矿成矿带是鲁西重要的成矿带,区内已发现李官集、彭集等多个大中型铁矿床,探明了铁矿石资源量超过12亿t。通过收集东平-汶上地区基础地质调查、区域重磁、矿产勘查、科研成果等资料,分析了区内地层、构造、岩浆岩及区域航磁异常特征、重力异常特征与铁矿床的对应耦合关系,提出了矿床的3个控矿因素:即控矿地层(泰山岩群雁翎关组、山草峪组,地层控矿专属性)、控矿构造(同斜复式背斜构造)、控矿岩浆岩(改造和破坏了铁矿带的完整性),通过对成矿区带样品采集测试,分别从主量元素、稀土元素、微量元素、原岩恢复、变质岩构造背景等方面进行系统分析对比,探讨了该区铁矿床为海相岛弧火山——沉积变质成因。 相似文献
269.
条带状铁建造(BIFs)中含有大量的亚铁磁性矿物,其组成及来源是认识BIF成因的重要依据。本文研究了南非巴伯顿绿岩带无花果树群(距今约32亿年)恩圭尼亚组的BIFs样品的磁学和矿物学特征。通过测量富铁层与富硅层的磁滞回线、等温剩磁获得曲线与退磁曲线、矫顽力谱分析、一阶反转曲线(FORC)、低温(20~300K)有场/无场冷却曲线以及k-T曲线、Lowrie三轴热退磁曲线,结合扫描电镜观测,揭示出研究样品中磁性矿物主要为赤铁矿和磁铁矿。基于矫顽力谱分析,富铁层中磁铁矿主要是多畴及假单畴颗粒,相对含量平均为2. 1%;赤铁矿的相对含量平均为97. 9%。富硅层中磁铁矿主要为假单畴及超顺磁性颗粒,相对含量平均为4. 6%;赤铁矿相对含量平均为95. 4%。测试样品具有Morin转变特征,转变温度介于250~260K,说明BIFs中主要为赤铁矿(0. 5~6mm)。富硅层样品出现~107K、~125K两个Verwey转变温度,表明其中可能存在生物成因和非生物成因两种类型磁铁矿。 相似文献
270.