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71.
通过野外采样、化学分析、电子探针(EPMA)和X射线衍射(XRD)分析等手段,研究了贵州织金地区黑色页岩矿物成分、化学组分、微量元素、稀土元素特征。研究区矿样化学成分以SiO_2和Al_2O_3为主,且具有高K低Na的特征。电子探针和X射线衍射分析表明,研究区黑色页岩主要矿物组成有石英、粘土矿物、白云石及黄铁矿等。织金黑色页岩中Pb、Ni、U、V、Cr等金属元素存在不同程度的富集,稀土元素总量为153.2×10~(-6)~224.89×10~(-6),属轻稀土元素富集型。同时从多金属层、页岩气、页岩提钾及近底部含磷铀矿资源等方面讨论了织金黑色页岩资源化利用。织金黑色页岩多金属层含有Mo、V、Ni、Ag及U等多金属元素,具综合利用价值;其中有机碳含量达到页岩气开发大于2%的条件,可进一步开展研究;页岩中伊利石含量较多,可提取黑色页岩中的钾制备含钾复合肥;黑色页岩底部与磷矿层接触带产出磷铀矿,主要为胶状磷铀矿,接触带可作为铀矿找矿的标志层。  相似文献   
72.
Copper speciation in a collection of Japanese geochemical reference materials (JSO‐1, JLk‐1, JSd‐1, ‐2, ‐3 and ‐4, JMs‐1 and JMs‐2) was achieved by sequential extraction and characterised using X‐ray absorption near‐edge structure spectroscopy. In the first step of the extraction, referred to as the acid fraction, between 1% and 20% total Cu within the reference materials was extracted. Such a result is typically accounted for by absorption of Cu onto clay minerals. However, the presence of Cu sulfate (an oxidation product of chalcopyrite) was observed in some of the stream sediments affected by mining activity (JSd‐2 and JSd‐3) instead. Copper was extracted in the reducible fraction (targeting Fe hydroxide and Mn oxide) (2–49% total Cu). Between 2% and 51% Cu was extracted in the oxidised fraction (targeting sulfides and organic matter). X‐ray absorption near‐edge structure spectroscopy clarified that the reducible fraction consisted of Cu bound to Fe hydroxide, whereas the oxidised fraction was a mixture of Cu bound to humic acid (HA) and Cu sulfide. In the oxidisable fraction, chalcopyrite was the predominant species identified in JSd‐2, and Cu bound to HA was the major species identified in JSO‐1 (a soil sample).  相似文献   
73.
In this article, we document a detailed analytical characterisation of zircon M127, a homogeneous 12.7 carat gemstone from Ratnapura, Sri Lanka. Zircon M127 has TIMS‐determined mean U–Pb radiogenic isotopic ratios of 0.084743 ± 0.000027 for 206Pb/238U and 0.67676 ± 0.00023 for 207Pb/235U (weighted means, 2s uncertainties). Its 206Pb/238U age of 524.36 ± 0.16 Ma (95% confidence uncertainty) is concordant within the uncertainties of decay constants. The δ18O value (determined by laser fluorination) is 8.26 ± 0.06‰ VSMOW (2s), and the mean 176Hf/177Hf ratio (determined by solution ICP‐MS) is 0.282396 ± 0.000004 (2s). The SIMS‐determined δ7Li value is ?0.6 ± 0.9‰ (2s), with a mean mass fraction of 1.0 ± 0.1 μg g?1 Li (2s). Zircon M127 contains ~ 923 μg g?1 U. The moderate degree of radiation damage corresponds well with the time‐integrated self‐irradiation dose of 1.82 × 1018 alpha events per gram. This observation, and the (U–Th)/He age of 426 ± 7 Ma (2s), which is typical of unheated Sri Lankan zircon, enable us to exclude any thermal treatment. Zircon M127 is proposed as a reference material for the determination of zircon U–Pb ages by means of SIMS in combination with hafnium and stable isotope (oxygen and potentially also lithium) determination.  相似文献   
74.
This article investigates the influence of dimensions of a settling column on the settling mode and the settling rate. End conditions of the settling stage in the hindered settling were also analyzed. It was found that the settling mode in a column with a smaller diameter tends to be consolidation settling. The effect of a settling column wall decreases with increasing column diameter, and it can be ignored provided the column diameter is larger than 14.5 centimeters. For the difference in initial water content, the settling behavior of the slurry develops a different sensitivity to the diameter effect. The influence of column diameter reduces as the initial water content of the slurry becomes higher. It is suggested that the internal diameter of the column used in a sedimentation experiment should be 14.5 centimeters.  相似文献   
75.
在煤层气勘探井固体岩心钻探施工过程中,遇岩层构造发育、地下水系发达的施工条件,钻进中往往发生钻井多层漏失、护壁困难的情况。因煤层气勘探井对录井工作的特殊要求,护壁堵漏工作的成功与否成为钻探施工的关键。在进行钻井护壁堵漏处理时,因技术方法不得当或未采取正确的计算经常导致护壁堵漏失败,甚至引发重大的钻探事故。通过对工区施工的经验总结,提出了切实可行的护壁堵漏技术措施,为类似地层钻井勘探施工提供借鉴。  相似文献   
76.
Solid matrix 3H reference materials are challenging to prepare given the volatile nature of 3H and are often unrepresentative of the range of 3H forms that may be encountered during routine analysis. As a result, few 3H reference materials are currently available, undermining verification of analytical techniques for environmental 3H measurement. To address this, an International Working Group on Organically‐Bound Tritium Analysis determined to produce a tritium natural matrix reference material (NMRM). The reference material comprises marine sediment blended with sewage sludge contaminated with 3H‐organic species arising from authorised discharges from a radiopharmaceutical manufacturing site. Previous studies have demonstrated that the 3H species have persisted in the environment over three decades providing valuable supporting data to underpin the characterisation of the NMRM. The preparation and characterisation of the NMRM are described along with the subsequent application of the reference material in an international intercomparison exercise involving nineteen laboratories from nine countries. A reference value of 168 ± 22 Bq kg?1 was derived from the data arising from the proficiency test.  相似文献   
77.
A new natural rutile reference material is presented, suitable for U‐Pb dating and Zr‐in‐rutile thermometry by microbeam methods. U‐Pb dating of rutile R632 using laser ablation ICP‐MS with both magnetic sector field and quadrupole instruments as well as isotope dilution‐thermal ionisation mass spectrometry yielded a concordia age of 496 ± 2 Ma. The high U content (> 300 μg g?1) enabled measurement of high‐precision U‐Pb ages despite its young age. The sample was found to have a Zr content of 4294 ± 196 μg g?1, which makes it an excellent complementary reference material for Zr‐in‐rutile thermometry. Individual rutile grains have homogeneous compositions of a number of other trace elements including V, Cr, Fe, Nb, Mo, Sn, Sb, Hf, Ta and W. This newly characterised material significantly expands the range of available rutile reference materials relevant for age and temperature determinations.  相似文献   
78.
蔡光耀  安芳  袁轶  刘芳  刘炜  张京渤 《地质学报》2021,95(5):1561-1572
八卦庙金矿床位于秦岭造山带凤太铅锌多金属矿田北部,是陕西省规模较大的金矿床之一,已探明金储量约106 t.赋矿围岩是上泥盆统星红铺组浅变质泥质碎屑岩和碳酸盐岩,其成矿过程可划分为3期,分别是①顺层磁黄铁矿-石英成矿期;②NE向黄铁矿-石英成矿期;③裂隙硫化物-方解石成矿期.目前关于NE向黄铁矿-石英成矿期成矿物质来源和成矿机制仍存在争议.本文通过矿相学观察,将NE向黄铁矿-石英成矿期划分为自形磁黄铁矿-黄铁矿-粗粒石英阶段(Ⅰ)、他形黄铁矿-银金矿-细粒石英阶段(Ⅱ)、他形磁黄铁矿-自然金-方解石阶段(Ⅲ)和黑云母阶段(IV),并在此基础上采用激光剥蚀-多接收等离子体质谱(LA-MC-ICP-MS)分析方法对千枚岩围岩中以及不同阶段形成的硫化物进行了原位S同位素测试,结果显示围岩中原生磁黄铁矿的δ34 S值集中于11.6‰~13.0‰之间,介于前人报道的原生黄铁矿δ34 S值变化范围(3.3‰~16.0‰);阶段I形成的黄铁矿的δ34 S值为8.4‰~10.1‰,磁黄铁矿为7.6‰~8.0‰;阶段II黄铁矿的δ34 S值相对较高,为14.0‰~15.9‰;阶段Ⅲ磁黄铁矿的δ34 S值介于6.4‰~8.3‰之间.八卦庙金矿NE向黄铁矿-石英成矿期总体相对富集重硫同位素、离散程度较大,各阶段硫化物的硫同位素值介于矿集区花岗岩和围岩硫之间,显示其具有岩浆硫与地层硫混合的特征.结合阶段I到阶段Ⅲ矿物组合的变化(黄铁矿+磁黄铁矿→黄铁矿→磁黄铁矿),推断阶段IIδ34 S值增高是水岩反应引起的硫化作用所致,而阶段Ⅲ硫同位素值降低可能与岩浆水的加入密切相关.结合成矿物理化学条件,推断该成矿期成矿热液中金主要以Au(HS)2-的形式迁移,阶段I到阶段Ⅱ由水岩反应引起的硫化作用是导致他形黄铁矿-银金矿-细粒石英阶段(Ⅱ)金矿化的主要原因,而岩浆水的混入可能是导致他形磁黄铁矿-自然金-方解石阶段(Ⅲ)金沉淀的主要机理.  相似文献   
79.
柴北缘赛坝沟金矿床是青海省赛什腾山-阿尔茨托山成矿带上重要的岩金矿床,成矿地质条件优越。矿体赋存于北西-北北西向韧-脆性断裂构造组内,呈脉状、透镜状,构造控矿作用明显,矿石类型分为石英脉型和蚀变糜棱岩型。热液成矿期可划分为4个阶段:Ⅰ少量黄铁矿-烟灰色石英阶段、Ⅱ金-黄铁矿-乳白色石英阶段、Ⅲ多金属硫化物-金-灰白色-灰褐色石英阶段、Ⅳ灰白色-浅肉红色石英-碳酸盐岩阶段。文章基于各热液成矿阶段硫化物的硫、铅同位素研究,探讨了赛坝沟金矿床成矿物质来源。研究结果表明,赛坝沟金矿床矿石中硫同位素在0.50‰~3.93‰之间,分布集中,通过与区域矿床围岩及成矿后石英脉硫同位素值(3.7‰~4.0‰)进行比较,认为赛坝沟金矿中的硫除来自于围岩外,更多来自于深部的幔源流体;铅同位素组成特征分析表明,赛坝沟金矿床矿石铅主要来源于深部地幔与下地壳铅混合,也有少量上地壳铅的参与,而围岩铅主要来源于上地壳。  相似文献   
80.
王尧  田衎  封跃鹏  王伟 《岩矿测试》2021,(4):593-602
土壤环境标准样品是土壤生态环境监测质量控制的重要技术工具。目前,土壤中总有机碳环境标准样品仍为中国环境标准样品体系的空缺,特别是配套燃烧氧化-非分散红外法的土壤标准样品一直未曾问世。本文以有机碳含量较高的农用地土壤为原材料,经干燥、研磨、混匀、装瓶、灭菌等加工步骤,制备获得土壤中总有机碳环境标准样品。分层随机抽取10瓶样品进行均匀性检验,经评价统计量F小于临界值F_(0.05)(9,10),瓶间均匀性相对不确定度(u_(bb))为1.5%,样品均匀性良好。在室温避光保存条件下,对样品进行了18个月的稳定性检验,稳定性相对不确定度(u_(lts))为1.2%,样品具有良好稳定性。由中国11家实验室采用燃烧氧化-非分散红外法和重铬酸钾容量法进行协作定值,通过对检测结果的数理统计分析,样品量值评定结果为(25.2±1.4)mg/g。该标准样品为采用燃烧氧化-非分散红外法参与定值的土壤中总有机碳环境标准样品,可作为土壤中总有机碳测定标准方法配套的实物标准,满足土壤生态环境监测及相关研究需求,且与国外同类样品具有可比性。  相似文献   
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