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101.
林南仓属于低瓦斯矿井,但存在高瓦斯区域。煤层和采空区是瓦斯的主要来源,尤以采空涌出量大,给煤矿生产和安全带来了极大隐患。通过在1129综采工作面风道施工高位瓦斯孔,把钻孔打到采空区一侧煤层顶板以上冒落裂隙带内,用钻孔进行瓦斯抽放,使采空内的瓦斯通过裂隙带沿钻孔抽出,有效降低综采工作面瓦斯浓度,保证综采工作面正常回采和安全生产。 相似文献
102.
通过对焦煤集团九里山矿14101工作面底板突水经过的研究,认为工作面底板突水的水源是是Lg灰岩水,其直接补给水源为L2灰岩水,间接补给水源为O2灰岩水;导水通道为底板采动裂隙带。采取了在工作面打水闸墙,利用钻孔对采空区灌注骨料,增加水流阻力,切断导水通道,封堵水源,加固隔水层的地面注浆和井下工程相结合的综合治水方案。通过观察,工作面中间巷无水流出,突水前后水位变化明显,在较短时间内获得了堵水成功。取得了显著的经济效益和社会效益,为矿井突水治理积累了经验。 相似文献
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采用SPSS软件,对2003年01月至2004年12月期间,倒天河水库和利民水库逐月水质监测数据进行数理统计分析,结果表明毕节市饮用水水质污染有较明显的季节变化和空间差异;且不同污染物对水体污染的贡献率各不相同,总磷和粪大肠菌群所占份额最大,方差累积贡献率达77%。在此基础上,利用加权综合污染指数对水体水质污染现状进行综合评价,结果显示倒天河水库和利民水库,水质污染总体较轻.饮用水水质符合《地表水环境质量标准(GB3838—2002)》中Ⅲ类水质标准;最后提出加大水环境保护的建议。 相似文献
106.
四川盆地三叠系地下水可划分出碎屑岩孔隙裂隙和碳酸盐岩岩溶裂隙两大储集类型。按此处构造开启程度和埋深条件等的不同,下中三叠统地下水有沉积变质水和渗入淋滤水两种基本成因类型,水动力特征各异。沉积变质水处于深埋封闭条件,受地静压力驱动控制;渗入淋滤水分布于背斜露头区和浅部地区,受静水压力驱动控制。并由此控制了盆地三叠系盐类的保存条件。 相似文献
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108.
Taoze LIU Yuangen YANG Bangyu LIU Xiangyang BI Feili LI 《中国地球化学学报》2006,25(B08):41-42
It has been found that stream waters were severely contaminated with wastes from a long-time smelting factory in Hezhang, Guizhou, China. The main sources of contamination are the smelting wastes stored in the open air and abandoned in the vicinity of stream. A method of lead isotope was adopted in order to identify relations between tailings and water contamination. Representative samples of tailings and stream sediments were collected. Mineralogical characterizations were conducted using XRD and TEM/SEM, while acid digestion was carried out for determining metal contents. BCR sequential leaching tests were performed in order to assess metal mobility. The tremendous ‘actual' and ‘potential' mobility of heavy metals indicates that the smelting waste and stream sediments present a considerable threat to the environment. Besides the chemical remobilization of heavy metals from the sediments and the reworking of riverbed sediments act as a secondary source of pollution. Also groundwater and stream water were sampled in specific locations and were measured. 相似文献
109.
Lichun LIU Yuting CHEN Kuanyu CHEN Jyhyih LEU Tsungkwei LIU 《中国地球化学学报》2006,25(B08):67-67
High concentrations of arsenic and humic substances in groundwater from the southwestern coastal plain of Taiwan were well known for their probable relationships with black-foot disease. In order to realize the relationships between the concentrations of humic substances and arsenic in this area, 24 well water samples were analyzed. After filtered through 0.45 μm glass fiber membrane in the field, samples were kept in the dark at 4℃ and then separated into six fractions with varying range of molecular weight (〈0.5, 0.5-1, 1-5, 5-10, 10-50 and 〉50 k Da) by ultrafiltration apparatus (Molecular/Por Stirred Cell system) in the lab. Concentrations of humic substances were measured by fluorescence spectrometer (HITACHI F-2000, ex=370, em=445) and arsenic by FIAS-AA (Perkin Elmer AAnalyst 100, FIAS-400). On average, only 6.2% of the total arsenic in water existed in the fraction of 〉0.5 k Da. and the others were complexed with humic substances (including humic acid and fulvic acid). The results demonstrated a distinct positive correlation between the concentrations of humic substances and arsenic. 相似文献
110.
Yoko Shimamoto Yoshio Takahashi 《中国地球化学学报》2006,25(B08):114-114
Although inorganic species are predominant in natural systems, but there are many kinds of organoarsenic species such as methylated and phenylated arsenic compounds. Phenylarsonic acid (PA) is a degradation product of organoarsenics used for chemical warfare agents, which has been detected in well water at the disposal site of the agents in Japan. There are few reports studying behavior of PA in soil. In this study, PA was adsorbed onto ferrihydrite and its chemical forms were determined using high performance liquid chromatography connected to inductivity-coupled plasma mass spectrometry (HPLC-ICP-MS). 100 mg/kg of PA was mixed with 0.03 g of 2-line ferrihydrite. For each suspension, pH was adjusted by HNO3 or NaOH. Each sample was incubated for more than 19 hours and the final pH was measured. After filtration, the chemical form of arsenic in the filtrate was measured using HPLC-ICP-MS. In addition, ferrihydrite separated by filtration was dissolved by 3 ml of 0.5 M HCI and the arsenic species in the solution was detected by HPLC-ICP-MS (column: Tosoh TSKgel SuperlC-AP, eluent: 0.01 M HNO3). It was verified that PA is not degraded by heating in 0.5 M HCl solution. At pH 3.1, any arsenic compounds were not detected from the solution, because almost all arsenic species were adsorbed onto ferrihydrite at lower pH. At pH= 12, however, 7%-10% of inorganic arsenic was detected in the solution. In solid phase, there are some problems to determine the precise ratio of inorganic and organic species. When the solution includes Fe ion at 0.01 M level, the retention time of arsenic species drifted compared to those in standard solution, which makes it difficult to determine precisely the arsenic species adsorbed on ferrihydrite. Therefore, more study is needed to determine the ratio of inorganic and organic species in the system. 相似文献