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161.
张维萍  赫英  董振信 《地球化学》2007,36(4):419-424
采集中国北方玄武岩中橄榄岩包体样品21件。测定了其中的主元素、微量元素、稀土元素(REE)和Au等的含量。橄榄岩包体中的Au含量与CaO含量的相关性表明,其中的Au可能主要赋存于单斜辉石中,反映Au含量可能与地幔演化及熔融程度有关;橄榄岩包体后期受地幔流体交代作用的影响,Au转而以硫化物形式存在,这一过程是在橄榄岩包体原有Au的物质基础上进行的。  相似文献   
162.
镁铁质-超镁铁质岩浆结晶分离早期形成镁铁矿物,镁铁矿物中的Ni和Mg是相容元素。随着结晶分离作用的进行,Ni、Mg在硅酸盐岩浆及后形成的硅酸盐物质中的丰度下降。橄榄石中Ni含量及硅酸盐物质MgO/FeO比值都与母岩浆的相关值相关,据此可推断母岩浆的信息,它们之间可由实验测得的系数相联系。当岩浆饱和硫化物时,在结晶分离过程中硫化物珠滴会与镁铁硅酸盐物质一道析出,同时,与硫化物非饱和岩浆相比,过多的Ni会随之析出。这也反映在Ni、Mg含量比无硫化物分离时有更迅速的降低上。Ni、Mg含量变化值可以在VoiseysBay侵入体的模式曲线上反映出,加拿大Labrador的这一侵入体赋存了一个世界级的Ni-Cu-Co硫化物矿床。过去的作法是将侵入体中橄榄石的Ni、Mg含量与Simkin和Smith得出的各种火成岩中橄榄石的Ni、Mg含量相比较以确定Ni亏损,进而假定橄榄石来自硫化物饱和、有经济价值的岩浆。现在的研究显示这种简单的对比会导致错误。将样品数据与模式曲线对比并反映出侵入体矿物结晶堆积特征是重要的方法。使用这一方法,样品数据能很好地被模式曲线拟合。以在VoiseysBay的研究为例,当硫化物液相与硅酸盐矿物被去除后,硫化物非饱和的分离作用期就会显现出来,随后是硅酸盐结晶作用期。  相似文献   
163.
The distribution of platinum group elements (PGEs) in massive sulfides and hematite–magnetite±pyrite assemblages from the recently discovered basalt-hosted Turtle Pits hydrothermal field and in massive sulfides from the ultramafic-hosted Logatchev vent field both on the Mid-Atlantic Ridge was studied and compared to that from selected ancient volcanic-hosted massive sulfide (VHMS) deposits. Cu-rich samples from black smoker chimneys of both vent fields are enriched in Pd and Rh (Pd up to 227 ppb and Rh up to 149 ppb) when compared to hematite–magnetite-rich samples from Turtle Pits (Pd up to 10 ppb, Rh up to 1.9 ppb). A significant positive correlation was established between Cu and Rh in sulfide samples from Turtle Pits. PGE chondrite-normalized patterns (with a positive Rh anomaly and Pd and Au enrichment), Pd/Pt and Pd/Au ratios close to global MORB, and high values of Pd/Ir and Pt/Ir ratios indicate mafic source rock and seawater involvement in the hydrothermal system at Turtle Pits. Similarly shaped PGE chondrite-normalized patterns and high values of Pd/Pt and Pd/Ir ratios in Cu-rich sulfides at Logatchev likely reflect a similar mechanism of PGE enrichment but with involvement of ultramafic source rocks.  相似文献   
164.
The primary factors that control the concentration of total reduced (inorganic) sulfide in coastal sediments are believed to be the availability of reactive iron, dissolved sulfate and metabolizable organic carbon. We selected nine sites in shallow (<3 m), close to sub-tropical, estuaries and bays along the central Texas coast that represented a range in sediment grain size (a proxy for reactive iron), salinity (a proxy for dissolved sulfate), and total organic carbon (a proxy for metabolizable organic carbon). Based on these parameters a prediction was made of which factor was likely to control total reduced sulfide at each site and what the relative total reduced sulfide concentration was likely to be. To test the prediction, the sediments were analyzed for total reduced sulfide, acid volatile sulfide, and citrate dithionate-extractable, HCl-extractable and total Fe in the solid phase. Using solid-state gold–mercury amalgam microelectrodes and voltammetry, we determined pore water depth profiles of Fe(II) and ΣH2S and presence or absence of FeS(aq). At five of the nine sites the calculated degree of sufildization of citrate dithionite-reactive-iron was close to or greater than 1 indicating that rapidly reactive iron was probably the limiting factor for iron sulfide mineral formation. At one site (salinity = 0.9) dissolved Fe(II) was high, ΣH2S was undetectable and the total reduced sulfide concentration was low indicating sulfate limitation. At the last three sites a low degree of sulfidization and modest total reduced (inorganic) sulfide concentrations appeared to be the result of a limited supply of metabolizable organic carbon. Fe(II)–S(-II) clusters (FeS(aq)) were undetectable in 10 out of 12 bay sediment profiles where ΣH2S was close to or below detection limits, but was observed in all other porewater profiles. Acid volatile sulfide, but not total reduced sulfide, was well correlated with total organic carbon and ranged from being undetectable in some cores to representing a major portion of total reduced sulfide in other cores. Although predicted controls on total reduced sulfide were good for very low salinity water or sandy sediments, they were only right about half the time for the other sediments. The likely reasons for the wrong predictions are the poor correlation of total organic carbon with grain size and differing fractions of metabolizable organic carbon in different sedimentary environments. Differences in sediment accumulation rates may also play a role, but these are difficult to determine in this region where hurricanes often resuspend and move sediments. This study demonstrates the need to examine more complex and often difficult to determine parameters in anoxic “normal marine” sediments if we are to understand what controls the concentration and distribution of sulfides.  相似文献   
165.
郑志强  林东燕 《福建地质》2007,26(4):222-228
通过对闽西南地区石炭纪—早二叠世主要块状硫化物矿床的区域成矿背景、贮矿层位特征以及矿石矿物成分、结构构造,硫同位素地球化学特征、成矿温度等分析研究,指出该地区石炭纪—早二叠世块状硫化物矿床的形成多与海底火山活动有关,贮矿层中伴有典型的喷流沉积岩—硅质岩,并提出闽西南地区块状硫化物矿床存在海底喷流-沉积成矿作用的新认识。  相似文献   
166.
采用随机区组设计,以等价投入的常规化肥为对照,开展专用肥多点施肥试验研究.通过专用肥对林木生长量、林相特征的影响分析,结果表明:与等价投入(肥料成本)的常规化肥相比,施用系列专用肥的林分生长量均显著或极显著地高于常规化肥处理,且叶片浓绿、树势强壮,施后19个月内,树高、胸径、材积分别提高了7.8%~51.8%、9.8%~53.0%和30%以上,叶片叶绿素含量提高26.3%~94.2%,叶面积指数提高41.0%~172.8%.经对HA桉树专用肥的增产性、适应性和稳定性的综合分析与评定,选出基肥专用的优化配方为:有机质≥30.0%、N P2O5 K2O≥6.0%(2.5-2.0-1.5)、腐殖酸总量≥8.0%,并加上适量的"绿滴"复合微生物菌剂(于施用时和基肥按每50 kg∶1 kg的量掺入);追肥专用的优化配方为:有机质≥20.0%、N P2O5 K2O≥20.0%(9-8-3)、腐殖酸总量≥6.0%.  相似文献   
167.
A simulation was undertaken within a climatic chamber to investigate limestone dissolution under varied carbonic acid (H2CO3) strengths as a possible analogue for future increases in atmospheric CO2 arising from global warming. Twenty‐eight samples cut from a block of Bath (Box Hill) limestone from Somerville College, Oxford, which had been removed during restoration after 150 years in an urban environment, were weighed and placed in closed bottles of thin plastic containing varying concentrations of H2CO3. Half of the stone samples were derived from exposed surfaces of the stone block (weathered) while the others were obtained from the centre of the block on unexposed surfaces (unweathered). The purpose of this was to compare dissolution of previously weathered versus unweathered surfaces in strong (pH 4·73) versus weak (pH 6·43) solutions of H2CO3. A temperature of c. 19 °C was maintained within the chamber representing a plausible future temperature in Oxford for the year 2200 given current warming scenarios. The simulation lasted 25 days with a few stone samples being removed midway. Stone samples show reduced weight in all cases but one. There was greater dissolution of stone samples in a strong H2CO3 solution as conveyed by higher concentrations of total hardness and Ca2+ in the water samples as well as enhanced microscopic dissolution features identified using SEM. The simulation confirms that enhanced atmospheric CO2 under global warming, given adequate moisture, will accelerate dissolution rates particularly of newly replaced limestone building stones. However, previously weathered surfaces, such as those on historical stone exposed for a century or more, appear to be less susceptible to the effects of such increased rainfall acidity. Conservation techniques which remove weathered surfaces, such as stone cleaning, may accelerate future decay of historical limestone structures by increasing their susceptibility to dissolution. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   
168.
水资源中氯代烃污染物的去除方法   总被引:3,自引:0,他引:3  
李琳  刘菲 《黄金地质》2002,8(2):74-76
随着工业化的发展。氯代有机溶剂使用越来越广泛。并且难于去除。在20世纪90年代初期,人们就已认识到用Fe^0恢复污染的地下水的潜力。国外正在研究帮使用扔几种还原挥发性氯代烃的还原反应介质,尤其要提高的是双金属反应系统,反应速度快,而且脱Cl中国难解产物少,目前国也只停留在实验室研究阶段,个别做了地上反应器的验证实验,它的脱Cl机理、介质钝化和完全脱Cl问题还有待于进一步研究。  相似文献   
169.
水体中硫化物测定方法探讨   总被引:1,自引:0,他引:1       下载免费PDF全文
通过对测定硫化物标准曲线的质量保证及不同污染程度水样的前处理方法的探讨,得出硫化物标准溶液需现用现配及针对污染程度不同的水样分别采取直接测定、抽滤测定和酸化-吹气法测定的结论.  相似文献   
170.
张银龙 《陕西地质》2002,20(2):27-38
通过对山阳地区地层、构造、岩浆岩特征的论述 ,归纳总结了区内酸性—中酸性小岩体的空间分布、岩石类型、岩石主要矿物、岩石化学成分、岩石碱度、稀土元素、微量元素等特征 ,从五个方面提出了酸性—中酸性小岩体具有壳幔同熔成因的证据 ,分析总结了山阳小河口地区以酸性—中酸性小岩体成矿作用为主的多金属成矿规律 ,提出了成矿模式。  相似文献   
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