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71.
W. Swider 《Pure and Applied Geophysics》1988,127(2-3):403-414
The most meaningful way to compare observations of the daytimeD-region under all ionization conditions, for the purpose of improving our understanding of this region, would appear to be through use of the effective electron recombination coefficient, =q/[e]2, whereq is the ionization production rate, and where [e] is the electron concentration. This ratio apparently increases monotonically with decreasing altitude, and is much less variable than its componentsq and [e]. This parameter appears eminently suitable as a best first order solution to [e] after determiningq. For nighttime conditions, is more sensitive toq. However, an accurate but simple formula exists for the calculation of electron concentrations. 相似文献
72.
黄山东镁铁超镁铁杂岩中的辉石化学成分研究 总被引:7,自引:0,他引:7
通过对黄山东镁铁超镁铁杂岩的辉石化学成分研究,证明辉石的化学成分受寄主岩石类型的制约,从超镁铁岩相到角闪辉长岩相斜方辉石的化学成分由富MgO、SiO_2、Al_2O_3、Cr_2O_3到富FeO、TiO_2、CaO、MnO;单斜辉石化学成分由富Al_2O_3、Cr_2O_3、Na_2O、MgO到富FeO、MnO、CoO。在同一寄主岩石中,单斜辉石比斜方辉石富TiO_2、Al_2O_3、Cr_2O_3、CaO和Na_2O,贫MgO、SiO_2、MnO和FeO。根据辉石化学成分特征得出黄山东杂岩形成于岛弧环境,为上地幔石榴二辉檄榄岩部分熔融形成的拉斑玄武岩岩浆结晶分异作用的产物。 相似文献
73.
金川超镁铁质岩体矿物化学特征及矿物地质温度计、压力计研究 总被引:4,自引:0,他引:4
根据金川超镁铁质岩体主要造岩矿物和副矿物的共生组合关系及各种矿物的化学成分特点;选用5种较成熟、使用较方便的矿物地质温度计、压力计(主要是辉石温压计和角闪石压力计),对岩体形成的温、压条件进行了估算,其结果为:成岩温度为1000~1300℃(上限可到1400~1500℃),成岩压力约为5×10 ̄8~11×10 ̄8pa。金川超镁铁质岩体的主要岩石类型为尖晶石二辉橄榄岩,这一岩石类型在复杂体系相关系图中的稳定区域大致处于5×l0 ̄8~15×10 ̄8pa的范围,这与矿物温压计估算的成岩温压条件是一致的。 相似文献
74.
The chemical composition of lake water in Laguna Amarga, a small, shallow, saline lake near the Torres del Paine National Park (at 51°S), Chilean Patagonia, was studied in January, 1993. The water was strongly alkaline (pH 9.4) conductivity was 71.4 mS cm–1, and salinity was 77 g L–1. The major ions were sodium and sulphate. 相似文献
75.
Influence of fluid chemistry on shear-wave attenuation and velocity in sedimentary rocks 总被引:2,自引:0,他引:2
Dung Vo-Thanh 《Geophysical Journal International》1995,121(3):737-749
76.
Amino acid nitrogen in atmospheric aerosols: Occurrence,sources and photochemical modification 总被引:2,自引:0,他引:2
The presence of amino acids in atmospheric precipitation and aerosols has been noted for many years, yet relatively little is known about these or other nitrogen containing organic compounds in the atmosphere. Marine and continental rainwater analyses indicate that atmospheric aerosols, and subsequently atmospheric precipitation, may contain substantial levels of free and combined amino acids. The most likely source of amino N in the remote marine atmosphere appears to be the injection of proteinaceous material through the action of bursting bubbles at the sea-air interface or the long range transport from terrestrial sources. The capacity of these substrates to undergo photooxidation and photodegradation in the atmosphere to simpler species, such as ammonium ions, carboxylic acids, and for the S containing amino acids, oxidized forms of sulfur, has received little attention from atmospheric chemists. The photochemistry of covalently bound amino groups, particularly as found in peptides and amino acids, is discussed here with the purpose of summarizing what is known of their occurrence and their possible importance to atmospheric chemistry. 相似文献
77.
B. Chattopadhyay 《Mathematical Geology》1990,22(5):589-598
The Main Hill Arkasani Granophyre Pluton (MAG), a product of Proterozoic intraplate acid magmatic activity, represents an anatectic melt of the enveloping rocks of dominantly pelitic composition with subordinate trondhjemitic gneiss and basic rocks. Petrography, chemistry, correlation between compositional attributes, areal variation of volume percent granophyric intergrowth, and varimax rotated factor analysis of compositional attributes of these rocks suggest that in the MAG pluton, plagioclase phenocrysts and biotite crystallized first, followed by change of level of emplacement of the magma when the groundmass started crystallizing at a rapid rate. The rapid growth of quartz and alkali feldspar crystallizing from the residual melt gave rise to the ubiquitous granophyric intergrowth in the late stage of crystallization. The alkali-rich residual liquid tended to concentrate toward the margin of the pluton where there is a profusion of granophyric intergrowths. 相似文献
78.
Xue Xi Tie Guy Brasseur Xing Lin Pierre Friedlingstein Claire Granier Philip Rasch 《Journal of Atmospheric Chemistry》1994,18(2):103-128
The paper discusses the potential effects on the ozone layer of gases released by the engines of proposed high altitude supersonic aircraft. The major problem arises from the emissions of nitrogen oxides which have the potential to destroy significant quantities of ozone in the stratosphere. The magnitude of the perturbation is highly dependent on the cruise altitude of the aircraft. Furthermore, the depletion of ozone is substantially reduced when heterogeneous conversion of nitrogen oxides into nitric acid on sulfate aerosol particles is taken into account in the calculation. The sensitivity of the aerosol load on stratospheric ozone is investigated. First, the model indicates that the aerosol load induced by the SO2 released by aircraft is increased by about 10–20% above the background aerosols at mid-high latitude of the Northern Hemisphere at 15 km for the NASA emission scenario A (the NASA emission scenarios are explained in Tables I to III). This increase in aerosol has small effects on stratospheric ozone. Second, when the aerosol load is increased following a volcanic eruption similar to the eruption of El Chichon (Mexico, April 1982), the ozone column in spring increases by as much as 9% in response to the injection of NO
x
from the aircraft with the NASA emission scenario A. Finally, the modeled suggests that significant ozone depletion could result from the formation of additional polar stratospheric clouds produced by the injection of H2O and HNO3 by the aircraft engines. 相似文献
79.
为了研究东台吉乃尔盐湖卤水蒸发时的相化学,确定钾、镁和锂盐的结晶特性,在实验室内25℃等温蒸发实验基础上和自然条件下进行了冬夏季日晒蒸发试验.东台吉乃尔盐湖卤水是由氯化钠饱和的多组分复杂体系构成的.卤水中存在的离子是Na+、K+、Mg2+、Li+、Ca2+、B3+、SO42-和Cl-.试验数据与Na+、K+、Mg2+Cl-、SO42-KH2O五元体系介稳平衡数据进行了讨论和比较.Autenrieth相图被用来表示各数据间的关系和证明冬夏季蒸发时结晶行为的差别. 相似文献
80.
Summary The crystal structure of hendricksite, a trioctahedral mica of biotite type, characterized by high Zn2+ and Mn2+ contents has been refined by least square methods. The structural formula is: (K0.89Na0.10Ba0.04)(Mg1.57Zn0.54Mn
0.40
2+
Fe
0.25
2+
Al0.07Ti0.07Cr0.01)(Si2.92Al1.08)O10 (OH)2. The space group isC2/m and the cell parameters are:a=5.340(2) Å,b=9.524(2) Å,c=10.235(3) Å, =100.07(2)o, the cell volume isV=497.98 Å3. The final unweightedR=0.072. Average cation-anion distances in polyhedra are: T–O=1.659 Å, M(1)–O=2.093 Å, M(2)–O=2.088 Å, A–Olong=3.316 Å and A–Oshort=3.004 Å; A is the alkaline cation. The rotation angle of tetrahedra is =6.7°. The analysis of electron densities, of the dimensions and distorsions of polyhedra shows that Zn2+ is exclusively in octahedral sites; there is no order between six-fold coordinated cations. A comparison between the structural features of hendricksite and those of the two main end-members of biotites, phlogopite and annite, is presented.The effect of the strong covalence of Zn–O bonds is particularly visible on the dimensions and orientations of the thermal ellipsoids of octahedral sites M(1) and M(2) which contain zinc. In all the published structures of trioctahedral micas, the ellipsoids of cationic sites are uniaxial positive, elongated parallel toc
*. In hendricksite, this is observed only for the two zinc-free sites (T and A; in the octahedra M(1) and M(2), which contain zinc, the ellipsoids are approximately uniaxial negative, flattened parallel toa, which is a unique situation.Zinc which habitually favours the tetrahedral coordinations with oxygen, enters the octahedra only, i.e. the chemically anisotropic sites, in hendricksite. The strong polarizability of Zn2+ is proposed to explain this behaviour.An examination of the behaviour of Zn2+ in other compounds shows that this situation is general, zinc favours chemically anisotropic sites and specially those adjacent to OH or H2O.
Affinement de la structure cristalline de la hendricksite, mica trioctaédrique potassique riche en Zn et Mn; une contribution à la connaissance cristallochimique des minéraux zincifères
Résumé On a affiné par moindres carrés la structure de la hendricksite, mica trioctaédrique de type biotite, caractérisé par une teneur élevée en Zn2+ et Mn2+. La formule structurale de ce mica est: (K0m89Na0,10Ba0,04)(Mg1,57Zn0,54Mn 0,40 2+ Fe 0,25 2+ Al0,07Ti0,07Cr0,01)(Si2,92Al1,08)O10(OH)2. Le groupe spatial estC2/m et les paramètres de la maille:a=5,340(2) Å,b=9,254(2) Å,c=10,235(3) Å, =100,07(2)°; le volume de la maille estV=497,98 Å3. Le résidu final non-pondéré estR=0,072. Les distances cation-anion moyennes dans les polyèdres sont les suivantes: T–O=1,659 Å, M(1)–O=2,093 Å, M(2)–O=2,088 Å, A–Olong=3,316 Å et A–Ocourt=3,004 Å où A désigne le cation alcalin. L'angle de rotation tétraédrique, =6,7°, est très semblable à celui de la phlogopite. L'analyse des densités électroniques, des dimensions et distorsions des polyèdres montre que Zn2+ est exclusivement en coordinance octaédrique et qu'il n'y a pas d'ordre entre les cations hexacoordonnés. On présente une comparaison des caractères structuraux de la hendricksite avec ceux des deux principaux pôles des biotites, la phlogopite et l'annite.L'effet de la forte covalence de la liaison Zn–O est particulièrement visible sur les dimensions et orientations des ellipsoides d'agitation thermique des deux sites octaédriques, sites zincifères. Dans toutes les structures de micas trioctaédriques publiées, les ellipsoides des sites cationiques sont uniaxes positifs, allongés parallèlement àc *, ce qui s' observe effectivement dans les deux sites non-zincifères (T et A) de la hendricksite, par contre, dans les octaèdres M(1) et M(2), qui contiennent le zinc, les ellipsoides sont approximativement uniaxes négatifs, applatis parallèlement àa, ce qui est une situation unique.Le zinc, qui se fixe généralement en sites tétraédriques dans les structures de type oxyde, occupe les sites octaédriques, c'est-à-dire les sites chimiquement anisotropes dans la hendricksite. La forte polarisabilité de Zn2+ est proposée pour expliquer ce comportement.Un examen du comportement de Zn2+ dans d'autres phases montre que cette situation est tout à fait générale, le zinc privilégiant les sites chimiquement anisotropes et en particulier ceux adjacents à OH où H2O.相似文献