全文获取类型
收费全文 | 8974篇 |
免费 | 1780篇 |
国内免费 | 2665篇 |
专业分类
测绘学 | 798篇 |
大气科学 | 904篇 |
地球物理 | 1127篇 |
地质学 | 7018篇 |
海洋学 | 1800篇 |
天文学 | 46篇 |
综合类 | 728篇 |
自然地理 | 998篇 |
出版年
2024年 | 69篇 |
2023年 | 302篇 |
2022年 | 374篇 |
2021年 | 368篇 |
2020年 | 299篇 |
2019年 | 385篇 |
2018年 | 284篇 |
2017年 | 343篇 |
2016年 | 309篇 |
2015年 | 438篇 |
2014年 | 662篇 |
2013年 | 520篇 |
2012年 | 576篇 |
2011年 | 588篇 |
2010年 | 580篇 |
2009年 | 573篇 |
2008年 | 571篇 |
2007年 | 556篇 |
2006年 | 570篇 |
2005年 | 461篇 |
2004年 | 401篇 |
2003年 | 405篇 |
2002年 | 384篇 |
2001年 | 413篇 |
2000年 | 321篇 |
1999年 | 293篇 |
1998年 | 283篇 |
1997年 | 292篇 |
1996年 | 267篇 |
1995年 | 230篇 |
1994年 | 208篇 |
1993年 | 202篇 |
1992年 | 190篇 |
1991年 | 189篇 |
1990年 | 216篇 |
1989年 | 156篇 |
1988年 | 20篇 |
1987年 | 21篇 |
1986年 | 15篇 |
1985年 | 12篇 |
1984年 | 8篇 |
1983年 | 6篇 |
1982年 | 11篇 |
1981年 | 7篇 |
1979年 | 3篇 |
1978年 | 3篇 |
1976年 | 3篇 |
1975年 | 3篇 |
1958年 | 3篇 |
1954年 | 3篇 |
排序方式: 共有10000条查询结果,搜索用时 93 毫秒
181.
182.
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
183.
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
184.
库姆塔格沙漠"羽毛状沙丘"形态的示量特征 总被引:10,自引:2,他引:10
通过卫星照片判读和实地观测,库姆塔格沙漠的“羽毛状沙丘”由两种风沙地貌构成:东北-西南走向的新月形“沙垄”为“羽轴”;垄间分布的波状微起伏的“大沙波”为“羽枝”,“大沙波”与沙垄的夹角为75°~103°。二者组合成类似“羽毛”的风沙地貌。新月形“沙垄”由单个新月形沙丘的前一沙丘的迎风坡与后一沙丘东翼相连构成“沙垄”。组成“沙垄”的新月形沙丘的两翼平均长37.5m,翼间距30~66m,沙丘高3~19m;在所观测区域内,沙丘沙的分选性由南向北变差。新月形“沙垄”长为3~22km,垄间距为1~3km,其问分布浅色和暗色相间的波状微地貌,暗色部分平均宽24.3m,浅色部分的平均宽11.6m。暗色部分表层沙粒的粒径有60%在1.00~0.25mm之间,以暗色矿物为主,而浅色部分表层沙粒的粒径的90%在1.00~0.25mm之间,分选性相对暗色部分较好,以石英等浅色矿物为主。暗色和浅色微地貌成对出现,相对高差约7cm。这种波状微地貌在库姆塔格沙漠中北部重复出现,类似于风沙地貌分类的沙波,暂称其为“大沙波”。 相似文献
185.
186.
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
187.
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
188.
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
189.
Treatment of high fluoride concentration wastewater by layered double hydroxides: Mechanism studies 总被引:1,自引:0,他引:1
Liang LU Jing HE 《中国地球化学学报》2006,25(B08):160-161
An appropriate concentration of fluoride in drinking water is required to prevent dental cavities, but long-term ingestion of water that contains more than a suitable level of fluoride can cause bone disease and mottling of the teeth. Fluoride ions can be found in wastewater from the fluoride chemical industry, as well as the semiconductor, metal processing, fertilizer, and glass-manufacturing industries. The discharge standard for fluoride in industrial wastewater in China is 10 mg/L. Efficient treatment of fluoride-containing wastewater is therefore of major concern in China, following the rapid development of the fluoride chemical industry. Several methods have been used to remove fluoride from water, such as adsorption, chemical precipitation, electrodialysis, ion exchange and electrochemical processes. Layered double hydroxides (LDHs) are anionic clays with high anion exchange capacities which are effective adsorbents for removal of a variety of anionic pollutants. LDHs have been studied as potential adsorbents for removing toxic anionic species such as CrO4^2-, TcO4^-, SeO3^2-, pesticides, and anionic surfactants from aqueous systems. One of the main attractions of using LDHs for fluoride removal, is that unlike other chemical treatment methods, no chemical sludge should be produced. In the present study, an attempt was made to investigate the mechanism of fluoride removal by LDHs under different conditions using batch methods. In addition, the release of fluoride adsorbed on LDHs by treatment with an aqueous solution of Na2CO3 was studied. The residual fluoride was found to be 10 mg/L in a solution with an initial concentration of 1000 mg/L, which meets the discharge standard for fluoride in industrial wastewater in China. 相似文献
190.
Mohammad Rasul Jan Mahmood A Khawaja Jasmin Sha Kashif Gul 《中国地球化学学报》2006,25(B08):182-182
Due to the persistent nature of DDT, a persistent organic pollutant and its adverse environmental and health impacts, the present study was undertaken to examine the residual DDT in and around DDT manufacturing factory in Amman Gharh, Nowshera, NWFP. The factory was established in 1963 and remained in operation till 1994. Composite samples of soil, sediments and water were collected in and around the factory area, nearby DDT stores, main factory drain leading to river and nearby villages. Standard procedures were used for the collection, transportation and storage of samples for analysis. Physical parameters for the collected water samples measured were temperature, pH and conductance. Extraction of each sample for DDT analyses was carried out in triplicates using soxhlet extraction apparatus. The extract was transferred to well washed, clean; dry glass vial, sealed and put in the refrigerator. Gas Chromatograph with electron capture detector and capillary column was used for analysis. DDT in the samples was identified on the basis of their retention time and quantified on the basis of peak areas. It is evident from the analytical data obtained in the present study that both water and soil in and around the factory area are still contaminated with DDT, despite the closure of the factory since the past few years. 相似文献