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71.
湖泊是温室气体氧化亚氮(N2O)的潜在排放源,但由于自然环境以及人类活动的差异,其N2O排放规律也存在特殊性和地域性。为探究巢湖N2O排放通量的时空特征,利用静态暗箱-气相色谱法于2018年3月至2019年12月对巢湖不同区域(东、中、西)N2O的排放进行观测。结果表明,巢湖水体N2O年均排放通量为(25.14±55.01)μg/(m2·h),表现为N2O的“源”,且具有较为明显的时空分布规律。在时间分布上,季节变化趋势呈现“M”形模式,7月出现最小值且表现为N2O的“汇”((-12.97±16.32)μg/(m2·h)),在6月和8月为峰值,全年最大值出现在8月((68.25±78.05)μg/(m2·h)),极值均出现在夏季。在空间分布上,东、中、西3个湖区N2O排放通量差异显著(P=0.03),N2O排放通量最大值((4... 相似文献
72.
Manganese oxide has been widely investigated for oxidation of arsenite (As(III)) to arsenate (As(V)) due to its high redox potential; however, it becomes extremely unstable after reuse. Here, As(III) oxidation activity and stability of manganese oxide in the presence of peroxymonosulfate (PMS) is investigated. Batch experimental results reveal that manganese oxide/PMS exhibits high catalytic activity for As(III) oxidation compared to manganese oxide or PMS alone. Addition of PMS to manganese oxide not only reveals long‐term stability for As(III) oxidation, but also shows high As(III) oxidation activity in the presence of coexisting ions such as As(V) and phosphate. Quenching tests reveal that As(III) oxidation in the manganese oxide/PMS system is attributed to activation of PMS by manganese oxide at different oxidation states (Mn(III) and Mn(IV)), and the generation of sulfate radicals that are responsible for As(III) oxidation. 相似文献
73.
广西荣华锰矿位于三叠系百逢组,在该地层中发现的工业锰矿床尚未见报道。通过对该矿区大比例尺地质填图,并结合地质工程和测试分析等手段,对矿床地质背景、沉积环境、矿体和矿石特征、沉积演化等进行分析研究,推测荣华锰矿为沉积-淋滤锰帽型矿床,矿体顺层分布于靠近罗楼组碳酸盐岩的百逢组第一段泥岩、泥质粉砂岩中,严格受地层和构造控制。矿石主要由偏锰酸矿、软锰矿等组成,矿石品位偏低,伴生Co等金属元素。百逢组之下的碳酸盐岩和百逢组第一段浊积砾岩层可作为该类锰矿上下界线典型的找矿标志。中三叠世桂西北处于盆包台构造格局,中晚古生代富含锰的台地在三叠纪遭受风化剥蚀,成矿元素被带入弧后盆地。随着特提斯洋闭合,挤压作用使盆地面积变小,水位加深,氧化还原界面波动,在百逢组第一段锰元素初步富集。后右江盆地抬升露出水面遭受剥蚀,风化淋滤作用最终形成该区顺层分布的氧化锰矿床。桂西广泛出露百逢组地层,其第一段具有良好的找矿前景。 相似文献
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75.
There are two types of temporally and spatially associated intrusions within the Emeishan large igneous province (LIP); namely, small uitramafic subvolcanic sills that host magmatic Cu-Ni-Platinum Group Element (PGE)-bearing sulfide deposits and large mafic layered intrusions that host giant Ti-V magnetite deposits in the Panxi region. However, except for their coeval ages, the genetic relations between the ore-bearing intrusions and extrusive rocks are poorly understood. Phase equilibria analysis (Q-PI-OI-Opx-Cpx system) has been carried out to elucidate whether ore-bearing Panzhihua, Xinjie and Limahe intrusions are co-magmatic with the picrites and flood basalts (including high-Ti, low-Ti and alkali basalts), respectively. In this system, the parental magma can be classified as silica-undersaturated olivine basalt and silica-saturated tholeiite. The equivalents of the parental magma of the Xinjie and Limahe peridotites and picrites and iow-Ti basalts are silica-undersaturated, whereas the Limahe gabbro-diorites and high-Ti basalts are silica-saturated. In contrast, the Panzhihua intrusion appears to be alkali character. Phase equilibria relations clearly show that the magmas that formed the Panzhihua intrusion and high-Ti basalts cannot be co-magmatic as there is no way to derive one liquid from another by fractional crystallization. On the other hand, the Panzhihua intrusion appears to be related to Permian alkali intrusions in the region, but does not appear to be related to the alkali basalts recognized in the Longzhoushan lava stratigraphy. Comparably, the Limabe intrusion appears to be a genetic relation to the picrites, whereas the Xinjie intrusion may be genetically related to be low-Ti basaits. Additionally, the gabbro-diorites and peridotites of the Limahe intrusion are not co-magmatic, and the former appears to be derived liquid from high-Ti basalts. 相似文献
76.
Nowadays, the Fe-C coprecipitate mechanism is recognized by more and more scholars and becomes the hot topic in the environmental science. On the basis of discussing the interaction between iron oxide and organic matter, and the adsorption research progress of Fe-C complexes on heavy metals, the immobilization potential of Fe-C complexes on heavy metals in polluted soil were illustrated. The surface properties and physical characterizations of iron oxide are changed regularly with the interaction of organic matter, which lead to the higher adsorption capacity of Fe-C complexes in contrast to single iron oxide. Besides, the influences of pH values, organic matter types and surface properties of iron oxides on the adsorption capacity of Fe-C complexes on heavy metals were discussed. The excellent adsorption performance of Fe-C complexes in certain conditions will provide important theoretical basis for contaminated soil remediation. 相似文献
77.
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79.
建立了以纳米二氧化钛(TiO2)作为吸附剂填充微柱,电感耦合等离子体质谱(ICP-MS)法测试Cu^2+,Cd^2+,Pb^2+和Ni^2+离子的分析方法.考察了不同pH值、洗脱液浓度、样品流速、体积和外源干扰离子的影响,实验结果表明在pH值8~10范围内待测离子可被TiO2定量吸附,2.0molL^-1HNO3可将吸附在微柱上的待测物完全洗脱,优化条件下本方法对溶液中Cu^2+,Cd^2+,Ph^2+和M^2+离子检出限分别为:0.02,0.01,0.01,0.02μgL~,相对标准偏差小于2%(n=7),富集系数50倍.对水系沉积物标准物质(GBW07310)的测定值与标准值相一致,方法具有简便、快速,灵敏度高,重现性好的优点,可满足河口水体与沉积物样品中痕量金属元素定量分析的要求. 相似文献
80.
Lepidocrocite (γ‐FeOOH) nanoparticles were synthesized from iron(II) sulfate solution and characterized using X‐ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform‐IR (FT‐IR), nitrogen adsorption, and point of zero charge pH (pHPZC) analyses. TEM, XRD, and FT‐IR analyses proved the synthesis of nano‐lepidocrocite. Surface area and pHPZC of the synthesized lepidocrocite were 68.1 m2 g?1 and 4.8, respectively. Utilization of the synthesized lepidocrocite in the adsorption of Lanacron brown S‐GL (LBS‐GL) from aqueous solutions was investigated, and the effect of lepidocrocite dosage, pH, temperature, and contact time on this process were optimized and modeled using response surface methodology approach. The lepidocrocite dosage of 0.015 g, pH 3.5, temperature of 38°C, and contact time of 100 min were determined as optimum adsorption conditions. Isotherm and kinetics of the adsorption process were analyzed at the optimum conditions. The equilibrium data were fitted well to the Langmuir isotherm model. The maximum monolayer adsorption capacity was 528.21 mg g?1. The adsorption process was described by the pseudo‐second‐order kinetic model. Furthermore, the effect of pH on the desorption of LBS‐GL was investigated. High LBS‐GL desorption efficiency was achieved at a high pH value. 相似文献