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排序方式: 共有374条查询结果,搜索用时 26 毫秒
21.
李荣生 《华北地质矿产杂志》1994,9(4):405-410
沁县七星泉(后泉)饮用天然矿泉水是山西发现最早的天然矿泉水之一。1987年11月经国家级鉴定为低钠、低矿化度、锶重碳酸-钙镁型饮用天然矿泉水。可作为瓶装天然矿泉水及矿泉饮料用水予以开发。 相似文献
22.
Aspects of communities and events in the concentrating ponds (S.G. 1.130 to 1.214) and salt crystallizing ponds (S.G. 1.215 to 1.264) of solar saltworks pertinent to salt manufacture are described. Communities that aid salt manufacture enable continuous and efficient production of high quality salt at a saltworks' design capacity, and they provide important controls on levels of organic matter in the brine. Fluctuating salinities, high concentrations of nutrients, and petroleum products are disturbances that causeAphanothece halophytica andDunaliella salina to release excessive quantities of organic matter, and that suppress or cause death to nutrient stripping organisms. Disturbances result in decreased quality and quantity of salt and increased costs for salt harvest, washing, and pond upkeep. Organic matter can be controlled by management techniques that keep nutrient stripping communities at proper levels and maintain a narrow and unchanging range of salinities in each pond, by constructing pond dikes able to withstand wind and water erosion, and by preventing spills of petroleum products in the ponds. 相似文献
23.
J. P. McGreevy 《地球表面变化过程与地形》1985,10(5):509-518
Honeycomb weathering has been observed in a Carboniferous sandstone at a coastal location near Ballycastle on the north coast of Northern Ireland. Specimens of this sandstone have been analysed by X-ray diffraction, scanning electron microscopy, and energy dispersive spectrometry. Results reveal that calcium sulphate (gypsum) is the only salt present and is found only at and immediately below the rock surface. SEM observations suggest that crystallization of salts in pores could easily dislodge quartz grains to promote granular disintegration, whilst etching of quartz grain surfaces attests to chemical weathering activity within the rock However, the reason for the development of the honeycomb pattern is not known. 相似文献
24.
25.
热水沉积岩及矿物岩石标志 总被引:32,自引:2,他引:32
热水沉积物不同于普通沉积物 ,主要与热水流体类型有关。文中把热水流体划分为中高温热水流体与中低温热水流体。中高温热水沉积岩包括钾长石岩、硅质岩、电气石岩、钠长石岩、萤石岩 ;中低温热水沉积岩包括碳酸盐、硫酸盐等岩石。钾长石岩是文中确定的一种标准高温热水沉积岩 ,热水沉积钾长石以冰长石和钡长石为主 ;热水沉积碳酸盐矿物一般为铁、镁、锰、钙碳酸盐 ,碳酸盐的形成与CO2 和H2 O的不混溶温度有关 ,一般在不混溶温度 ,即 2 66℃以下生成 ,或在海水补偿线以上形成。热水沉积岩中有热水交代蚀变岩夹层 ,尤其是在高温热水活动区 ,可以交代泥质、钙泥质沉积物形成热水交代沉积岩 ,包括方柱石黑云母岩、透辉石透闪石岩、夕卡岩、绿泥石岩等。根据对霍各乞铜多金属矿床的研究 ,热水交代透辉石透闪石岩的稀土总量较低 ,表现为轻稀土富集 ,重稀土亏损 ,稀土配分模式表现为正Eu异常 相似文献
26.
On July 20, 1994, before the Q fragments of Comet Shoemaker-Levy 9 fell to Jupiter, more than 200 spectra of the Jovian features were obtained at the Crimean Astrophysical Observatory in the wavelength range 5700–7600 Å with a 26 s exposure time and a spectral resolution of 20 Å. We found a time-varying Na D line emission in the form of two components with Doppler shifts of about 30 Å. The brightest and most frequent sodium flares were detected when the Q fragments passed through the Jovian inner magnetosphere at a distance of about three the Jovian radii (3RJ) from its center, where they crossed the Io-Jupiter current tube. A frequency analysis of our data revealed a flare recurrence time scale of 1 min. We conclude that sodium was released from the cometary dust and from the surfaces of numerous cometary debris and that its amount was enough to produce the observed emission. The observed high-speed clouds of sodium atoms are assumed to have been formed through ionization, ion acceleration by the bidirectional electric fields of Alfvén waves in the Io-Jupiter current tube, and their neutralization. 相似文献
27.
微波消解-等离子体发射光谱法同时测定水中硅铁钠 总被引:1,自引:0,他引:1
讨论使用电感耦合等离子体发射光谱法测定水样中si、Fe、Na时,四种水样前处理方法对测试结果的影响。提出采用HNO3^-HF体系微波消解、H3BO3掩蔽HF的方法前处理水样,用等离子体发射光谱法可同时准确快速地测定水中Si、Fe、Na三种元素的含量。5次测定的相对标准偏差小于4%,加标回收率为89.2%-106%。 相似文献
28.
硫酸盐渍土在多次冻融循环时的盐胀累加规律 总被引:10,自引:3,他引:7
通过室内模拟试验,研究了硫酸盐渍土在历经多次冻融循环时的盐胀累加规律,得出了盐胀累加的不同类型,给出了累加盐胀率与循环次烽之间的关系式,进一步揭示了盐胀累加的 和影响因素。 相似文献
29.
Mobility of Al, Co, Cr, Cu, Fe, Mn, Ni and V in sulphide-bearing fine-grained sediments exposed to atmospheric O2: an experimental study 总被引:1,自引:0,他引:1
Mats Åström 《Environmental Geology》1998,36(3-4):219-226
The major aim was to increase our knowledge on the behaviour of Al, Co, Cr, Cu, Fe, Mn, Ni and V in sulphide-bearing fine-grained
sediments exposed to atmospheric oxygen. Samples of this type of sediment collected in a previous investigation at eight sites
in western Finland were digested in HClO4-HNO3-HCl-HF at 200 °C and in HCl:HNO3:H2O at 95 °C (aqua regia), and subjected to extractions with ammonium acetate and hydrogen peroxide. Metals and S in the leachates
were determined with ICP-AES. The results of the chemical analyses are compared with previously reported experimental data.
The concentrations of Al and Fe in the sulphide-bearing fine-grained sediments are about 7% and 5%, respectively. Of the trace
metals studied, Mn is most abundant followed in decreasing order by V>Cr>Ni>Cu>Co. On oxidation of the sediments, high proportions
of Co, Mn and Ni, intermediate proportions of Cu but low proportions of Fe, Al, Cr and V are released. The extent of the release
of a metal on oxidation is controlled either by (1) the level to which the pH of the sediments drops on oxidation (Al, Cu,
Cr, V), (2) the amount of the metal associated with easily reduced phases (metal sulphides) in the sediments (Ni, Co) or (3)
the sum of the amount associated with reduced phases and adsorbed on soil compounds (Mn). No control of the release of Fe
on oxidation of the sediments was identified. Based on the results of the study it is argued that artificial drainage and
the subsequent oxidation of sulphide-bearing sediments will result in extensive leaching of Co, Mn and Ni, moderate leaching
of Cu and limited leaching of Cr and V into drainages. The major elements, Fe and Al, have the potential to be mobilised and
leached in large amounts, though the proportions mobilised/leached will remain low. It is suggested that the identification
of sulphide-bearing sediments with a high potential of metal release should be based on determination of metals in easily
mobilised reduced compounds (dissolved e.g. in H2O2) and of the level to which the pH of the sediments drops on oxidation.
Received: 16 October 1997 · Accepted: 9 March 1998 相似文献
30.