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121.
Historical changes in sediments of Pyramid Lake,Nevada, USA: consequences of changes in the water balance of a terminal desert lake 总被引:1,自引:0,他引:1
Sediment cores from the shallow and deep basins of Pyramid Lake, Nevada, revealed variations in composition with depth reflecting changes in lake level, river inflow, and lake productivity. Recent sediments from the period of historical record indicate: (1) CaCO3 and organic content of sediment in the shallow basin decrease at lower lake level, (2) CaCO3 content of deep basin sediments increases when lake level decreases rapidly, and (3) the inorganic P content of sediments increases with decreasing lake volume. Variations in sediment composition also indicate several periods for which productivity in Pyramid Lake may have been elevated over the past 1000 years. Our data provide strong evidence for increased productivity during the first half of the 20th Century, although the typical pattern for cultural eutrophication was not observed. The organic content of sediments also suggests periods of increased productivity in the lake prior to the discovery and development of the region by white settlers. Indeed, a broad peak in organic fractions during the 1800's originates as an increase starting around 1600. However, periods of changing organic content of sediments also correspond to periods when inflow to the lake was probably at extremes (e.g. drought or flood) indicating that fluctuations in river inflow may be an important factor affecting sediment composition in Pyramid Lake. 相似文献
122.
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
123.
124.
Dispersion of Rayleigh-type surface wave is studied in a homogeneous transversely isotropic elastic layer overlying a nondissipative liquid-saturated porous solid half-space and lying under a uniform layer of homogeneous liquid. The frequency equation in the form of ninth-order determinant is obtained.Special cases have been deduced by reducing the depth of the layers to zero and by changing the transverse isotropic layer to an isotropic layer. Dispersion curves for the phase velocity have been plotted for a particular model. 相似文献
125.
126.
Wolfgang Junkermann Ulrich Platt Andreas Volz-Thomas 《Journal of Atmospheric Chemistry》1989,8(3):203-227
Photoelectric detectors for the measurement of photolysis frequencies of different trace gases in the atmosphere are described. They exhibit uniform response characteristics over one hemisphere (2 sr) and wavelength characteristics closely matched to those of the photolysis frequencies J
O1D, J
NO2, and J
NO3, respectively. Absolute calibration of the J
O1D detector was performed by chemical actinometry with an accuracy of ±16 percent. Simultaneous measurements of J
NO2 and J
O1D are presented. 相似文献
127.
A new experimental method is introduced for determining the relative magnitudes of liquid and vapor diffusion by using a small amount of soluble chemical as a tracer. The theoretical justification of the method is presented for the case where ice is absent. The feasibility of the method is demonstrated by an experiment using marine-deposited clay. 相似文献
128.
S. Madronich D. R. Hastie B. A. Ridley H. I. Schiff 《Journal of Atmospheric Chemistry》1984,1(2):151-157
The photodissociation coefficient, J
NO2 of NO2 in the atmosphere was calculated at 235 and 298 K using the measured temperature dependences of the absorption cross-sections and quantum yields. These calculations gave a ratio J
NO2(298 K)/J
NO2(235 K)=1.155±0.010 which is only weakly dependent on altitude, surface albedo and solar zenith angle. 相似文献
129.
本文主要讨论了岩浆不混溶的内在因素和物化条件。研究提出阳原杂岩大于零的过剩自由能是出现不混溶的内在原因。岩浆中高P_2O_5、TiO_2、Zr、Hf、Ta、REE是岩浆不混溶的诱导因素。化学位计算揭示了球状黑云辉石正长岩之球体、基质两相及正长质和辉石质岩浆单元在液态时曾处于平衡状态。岩浆不混溶可能是在温度约1200℃、上地壳深度范围内发生的。阳原母岩浆不混溶的两液相可以分离聚集成两大岩浆单元,岩浆分溶不充分,便产生中间成分的黑云辉石正长岩。 相似文献
130.
F. C. Fehsenfeld M. J. Bollinger S. C. Liu D. D. Parrish M. McFarland M. Trainer D. Kley P. C. Murphy D. L. Albritton D. H. Lenschow 《Journal of Atmospheric Chemistry》1983,1(1):87-105
The seasonal and diurnal variations of ozone mixing ratios have been observed at Niwot Ridge. Colorado. The ozone mixing ratios have been correlated with the NO
x
(NO+NO2) mixing ratios measured concurrently at the site. The seasonal and diurnal variations in O3 can be reasonably well understood by considering photochemistry and transport. In the winter there is no apparent systematic diurnal variation in the O3 mixing ratio because there is little diurnal change of transport and a slow photochemistry. In the summer, the O3 levels at the site are suppressed at night due to the presence of a nocturnal inversion layer that isolated ozone near the surface, where it is destroyed. Ozone is observed to increase in the summer during the day. The increases in ozone correlate with increasing NO
x
levels, as well as with the levels of other compounds of anthropogenic origin. We interpret this correlation as in-situ or in-transit photochemical production of ozone from these precursors that are transported to our site. The levels of ozone recorded approach 100 ppbv at NO
x
mixing ratios of approximately 3 ppbv. Calculations made using a simple clean tropospheric chemical model are consistent with the NO
x
-related trend observed for the daytime ozone mixing ratio. However, the chemistry, which does not include nonmethane hydrocarbon photochemistry, underestimates the observed O3 production. 相似文献