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71.
为了揭示磷(P)营养缺乏对蓝藻释放挥发性有机化合物(VOCs)的影响及其对其他藻类的化感作用,以形成蓝藻水华的主要种类铜绿微囊藻(Microcystis aeruginosa)为材料,在无P培养条件下对其释放的VOCs进行分析,同时测定VOCs对莱茵衣藻(Chlamydomonas reinhardtii)生长、光合色素含量和光合性能的影响.结果表明,采用无P培养基培养铜绿微囊藻24 h后,其释放的VOCs种类和含量均明显增加,与标准培养基培养相比,VOCs总释放量增加了73.4%,并出现7种新化合物.将铜绿微囊藻释放的VOCs通入莱茵衣藻溶液中,在标准培养基中铜绿微囊藻释放的VOCs对莱茵衣藻生长无显著影响,而无P条件下释放的VOCs则明显抑制莱茵衣藻生长,其响应指数(RI)为-0.25.此外,莱茵衣藻光合色素含量、光系统II(PSII)最大光化学量子产量(Fv/Fm)、有效光化学量子产量[Y(II)]、光化学淬灭系数(q P)和光合电子传递速率(ETR)也明显降低,而非光化学淬灭系数(NPQ)则明显升高,其RI为0.26.由此可见,蓝藻在富营养化水体中大量繁殖以及P自身沉降特性导致的P缺乏会促进蓝藻释放VOCs,同时这些VOCs在保持蓝藻营养竞争优势和水体藻类多样性减少中具有化感抑制作用. 相似文献
72.
73.
了解涂装行业挥发性有机物(VOCs)的排放特征是制定山东地区臭氧(O3)和PM2.5防控策略的重要环节.本研究在山东地区测定了两家典型食品金属包装企业喷涂过程中VOCs的排放组成,企业产品以饮料罐和罐头为主.结果表明:两家企业排放的总VOCs质量浓度水平相当,质量浓度变化范围在50~1 500 μg/m3;但两家企业喷涂过程中VOCs的排放组成具有一定的差异,以生产铝罐和马口铁罐为主的企业中的含氧挥发性有机物(OVOCs)含量最多,占比89.71%(质量分数,下同);而生产铝罐的企业芳香烃(56.15%)是首要的排放种类,其次是OVOCs (32.32%).通过分析两家企业内外喷涂工艺的VOCs源成分谱,发现同一企业不同工艺之间有一定差异,多种罐生产企业的内、外喷涂中乙醇占比最高,分别为94.28%、84.46%;单铝罐生产企业的内喷涂2-丁酮(24.33%)是重要组分,外喷涂中甲苯(36.40%)含量较高. 相似文献
74.
我国砷中毒病区的环境特征研究 总被引:18,自引:0,他引:18
我国饮水型砷中毒的流行屡见报道,台湾嘉南,新疆奎屯,内蒙古河套及山西大同等地是我国几个有代表性的病区。病区多为河湖相和滨海相沉积,粘土,粘土质淤泥和有机淤泥层发育,为富含有要质的还原环境,地下水中的含量一般为0.2-0.6mg/L。有时还有氟,腐殖酸,甲基胂酸和某些烷烃类等的有害有机化合物。 相似文献
75.
G. Figueres J.M. Martin M. Meybeck P. Seyler 《Estuarine, Coastal and Shelf Science》1985,20(2):183-203
Concentrations of mercury were determined for the waters, suspended matter and sediments of the Tagus and of major French estuaries.The Tagus estuary is one of the most contaminated by mercury derived from the outfalls of a chloralkali plant and from other industrial sources. In deposited sediments the median level, 1·0 μg Hg g?1, is twenty times higher than the natural background and Hg contents depend on the sediment grain-size, age and the distance from waste-outfalls. Suspended matter is more regularly and highly contaminated (median value: 4·5 μg Hg g?1). In the French estuaries Hg levels in the suspended material decrease with salinity due to dilution and/or remobilization processes. In June 1982, in the Loire estuary, high values of Hg are observed in the middle estuary and attributed to urban and industrial sources.In the Tagus estuary, the general distribution of total dissolved Hg confirms the contamination: it increases seaward from 10 ng 1?1 in the river to 80 ng 1?1 in the estuary outlet. The dissolved Hg is almost totally organic in the river, inorganic in the middle estuary due to inorganic Hg effluents and again organic in the lower estuary. This variation is related to the dissolved organic carbon values. The dissolved Hg levels in the Loire Estuary (5–300 ng 1?1) are much higher than in the Gironde estuary (3–6 ng 1?1) and of the same order as those observed in the Tagus estuary. 相似文献
76.
Effects of groundwater level fluctuation on its chemical composition in karst soils of Lithuania 总被引:3,自引:0,他引:3
Groundwater regime and mineralization process in moraine sandy loam and peat soils of the active sulphatic karst zone (karst
processes develop in the Upper Devonian gypsum–dolomites) in Lithuania and the dependence of chemical compounds concentrations
on water level fluctuations are reviewed. According to ion sum, groundwater mineralization in peat soil is 1.1–1.3 times higher
than in loam soil. Based on this result, lower levels of groundwater predetermine a more intensive mineralization process.
A stronger correlation was determined between groundwater levels and concentrations of chemical compounds (Ca2+, Mg2+, SO4
2− and HCO3
−) enhancing groundwater mineralization. In mineral soil (sandy loam) nitrate (NO3)− concentration is highly influenced by changing stages of groundwater level as well as by nearby sinkholes. 相似文献
77.
Multiple chemical constituents (nutrients; N, O, H, C stable isotopes; 64 organic wastewater compounds, 16 pharmaceutical
compounds) and microbiological indicators were used to assess the impact on groundwater quality from the land application
of approximately 9.5 million liters per day of treated municipal sewage effluent to a sprayfield in the 960-km2 Ichetucknee Springs basin, northern Florida. Enriched stable isotope signatures (δ18O and δ2H) were found in water from the effluent reservoir and a sprayfield monitoring well (MW-7) due to evaporation; however, groundwater
samples downgradient from the sprayfield have δ18O and δ2H concentrations that represented recharge of meteoric water. Boron and chloride concentrations also were elevated in water
from the sprayfield effluent reservoir and MW-7, but concentrations in groundwater decreased substantially with distance downgradient
to background levels in the springs (about 12 km) and indicated at least a tenfold dilution factor. Nitrate-nitrogen isotope
(δ15N–NO3) values above 10 ‰ in most water samples were indicative of organic nitrogen sources except Blue Hole Spring (δ15N–NO3 = 4.6–4.9 ‰), which indicated an inorganic source of nitrogen (fertilizers). The detection of low concentrations the insect
repellent N,N-diethyl-metatoluamide (DEET), and other organic compounds associated with domestic wastewater in Devil’s Eye Spring indicated
that leakage from a nearby septic tank drainfield likely has occurred. Elevated levels of fecal coliforms and enterococci
were found in Blue Hole Spring during higher flow conditions, which likely resulted from hydraulic connections to upgradient
sinkholes and are consistent with previoius dye-trace studies. Enteroviruses were not detected in the sprayfield effluent
reservoir, but were found in low concentrations in water samples from a downgradient well and Blue Hole Spring during high-flow
conditions indicating a human wastewater source. The Upper Floridan aquifer in the Ichetucknee Springs basin is highly vulnerable
to contamination from multiple anthropogenic sources throughout the springs basin. 相似文献
78.
Superfine graphite powder was prepared by ball-milling exfoliated graphite containing anhydrous CuCl2 in planetary ball milling systems. Nano-scale CuCl2 graphite intercalation compounds were synthesized by heating a mixture of anhydrous CuCl2 and graphite nanosheets. Scanning electron microscopy, energy-dispersive X-ray spectroscopy and high-resolution transmission electron microscopy were performed to characterize the microstructures of stage-1 nano-scale CuCl2 graphite intercalation compounds. The structure and components of the domain wall and core in the nano-scale CuCl2 graphite intercalation compounds are described. The results show that the content of CuCl2 in the mixture plays a crucial role in the size of the nano-scale CuCl2 graphite intercalation compound. 相似文献
79.
J. Kesselmeier 《Journal of Atmospheric Chemistry》2001,39(3):219-233
Field and laboratory investigations of the exchange of the short-chain organic acids – formic acid and acetic acid – as well as their homologous aldehydes are discussed. Both acids are substantially released from several plant species. Emission measurements under field conditions are compiled to give an overview of three years of measurements. Emission rates from several tree species were found in the range between zero and 60 nmoles m–2 min–1 for acetic acid and between zero and 90 nmoles m–2 min–1 for formic acid though also a deposition has been observed to orange trees. Investigations under laboratory conditions showed an order of magnitude lower emission rates with significant differences under light and dark conditions, and a deposition was observed under certain conditions. Hence, low emission rates or even a bi-directional exchange, emission as well as deposition have to be taken into account. Further differences between field and laboratory studies are discussed considering age of trees, stress effects and a potential production of acids by photochemical conversion of precursors inside enclosures during sampling. Field data on the exchange of form- and acetaldehyde show a complex behavior. We found emission as well as uptake. The bi-directional exchange is significantly triggered by the ambient mixing ratios of both aldehyde species and exhibits a compensation point. Further studies are needed for generalization of the exchange of these and potentially also for other compounds. 相似文献
80.
氢化物发生—原子荧光法直接测定锑及其化合物中的铅 总被引:1,自引:0,他引:1
通过在样品处理阶段用HBr除去大量锑基体,实现了不需再通过其他化学分离直接运用氢化物发生-原子荧光法测定锑及其相关产品中的微量铅,并用于实际样品的分析.该方法对样品检测下限小于10-6,在实际样品分析中,分析结果与原子吸收法测定结果之间无显著性差异,RSD<2.0%(n=4),对样品分析的加标回收率在95%~105%. 相似文献