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1.
Experimental solidification of anhydrous latitic and trachytic melts at different cooling rates: The role of nucleation kinetics 总被引:1,自引:0,他引:1
Gianluca Iezzi Silvio Mollo Guido Ventura Andrea Cavallo Claudia Romano 《Chemical Geology》2008,253(3-4):91-101
Two sets of cooling experiments were run at atmospheric conditions for two anhydrous starting latitic and trachytic melts: 1) five cooling rates (25, 12.5, 3, 0.5, and 0.125 °C/min) between 1300° and 800 °C, and 2) a 0.5 °C/min cooling rate from 1300 °C with quench temperatures at 1200°, 1100°, 1000° and 900 °C. Trachytic run-products are invariably glassy. Nucleation is also suppressed in the latitic run-products at the three highest cooling rates. Conversely, in the 0.5 and 0.125 °C/min runs, latites have a crystal content of 90 vol.%. The phases are: plagioclase, clinopyroxene, glass and iron-bearing oxide (in order of abundance). The variable quench temperatures, investigated by coupling experiments with Pt wire and Pt capsule sample containers in set 2, again did not produce crystallization of trachyte, whereas latitic samples are characterized by 10 vol.% of oxides, pyroxenes and plagioclase (in order of appearance), at temperature < 1000 °C. Effects of (preferential) heterogeneous nucleation on sample holders, of superheating degree, and chemical species loss during cooling are absent for both melt compositions. The difference of solidification paths between these two silicate melts can be ascribed only to their small chemical differences. In comparison with calculated equilibrium conditions all the experimental latitic and trachytic run-products revealed strong kinetic effects, interpretable in the light of the nucleation theory. The glass-forming ability (GFA) of trachyte is higher, whereas their critical cooling rate (Rc) is lower (< 0.125 °C/min), in comparison to latitic melts (Rc > 0.5 °C/min). The experimental results carried out in this study can be applied to lava flows and domes; trachytic lavas are able to flow for longer period with respect to latitic ones in a metastable condition. Glass-rich terrestrial lavas, i.e. obsidians, can be the result of sluggish nucleation kinetics due to the relative high polymerisation of evolved silicate melts. 相似文献
2.
Santschi Peter H. Honeyman Bruce D. Quigley Matthew S. 《Aquatic Sciences - Research Across Boundaries》1993,55(4):230-239
In 1975 Paul Schindler produced the first oceanic trace metal scavenging model to explicitly include the role of surface chemistry as a control on trace metal water column residence times. The eighteen years that have elapsed since the publication of Schindler's seminal paper have seen the development of a variety of oceanic scavenging models; yet, the fundamental insight of his Zero-order Model remains the benchmark. This paper describes the role of Paul Schindler's work on surface chemistry in providing a framework for the current generation of trace element scavenging models. 相似文献
3.
In Gaborone, as in other large cities in the developing world, individuals try to make a living by engaging in novel occupations
such as landfill scavenging. This paper reports on a research conducted in the Gaborone landfill, the largest in Botswana.
The study content-analyzed available literature from other countries. It also relied mainly on direct field observations.
The discussions on and answers to closed and interview schedules by stakeholders, affected- and- interested – persons, provided
the information on the threats and opportunities related to the landfill site and its informal management activities. This
on-going case study lends credence to the potential of scavenging in sustaining livelihoods among those who cannot secure
employment in the formal urban market. Scavenging tends to be useful although it may hazardous to the informal entrepreneurs.
Taking all the threats into consideration, the decommissioning and closure of the landfill seems inevitable, in spite of the
apparent short-term livelihood opportunities it provides to the informal sector. 相似文献
4.
In the metamorphic cores of many orogenic belts, large macroscopic folds in compositional layering also appear to fold one or more pervasive matrix foliations. The latter geometry suggests the folds formed relatively late in the tectonic history, after foliation development. However, microstructural analysis of four examples of such folds suggests this is not the case. The folds formed relatively early in the orogenic history and are the end product of multiple, near orthogonal, overprinting bulk shortening events. Once large macroscopic folds initiate, they may tighten further during successive periods of sub-parallel shortening, folding or reactivation of foliations that develop during intervening periods of near orthogonal shortening. Reactivation of the compositional layering defining the fold limbs causes foliation to be rotated into parallelism with the limbs.Multiple periods of porphyroblast growth accompanied the multiple phases of deformation that postdated the initial development of these folds. Some of these phases of deformation were attended by the development of large numbers of same asymmetry spiral-shaped inclusion trails in porphyroblasts on one limb of the fold and not the other, or larger numbers of opposite asymmetry spirals on the other limb, or similar numbers of the same asymmetry spirals on both limbs. Significantly, the largest disparity in numbers from limb to limb occurred for the first of these cases. For all four regional folds examined, the structural relationships that accompanied these large disparities were identical. In each case the shear sense operating on steeply dipping foliations was opposite to that required to originally develop the fold. Reactivation of the folded compositional layering was not possible for this shear sense. This favoured the development of sites of approximately coaxial shortening early during the deformation history, enhancing microfracture and promoting the growth of porphyroblasts on this limb in comparision to the other. These distributions of inclusion trail geometries from limb to limb cannot be explained by porphyroblast rotation, or folding of pre-existing rotated porphyroblasts within a shear zone, but can be explained by development of the inclusion trails synchronous with successive sub-vertical and sub-horizontal foliations. 相似文献
5.
无锡梅雨期湿沉降综合分析 总被引:2,自引:0,他引:2
利用2008—2014年梅雨期间酸雨观测资料及2014年6月16—27日降水个例加密采样资料,结合大气污染物资料分析了近7 a无锡梅雨期酸雨特征,研究降水过程中空气污染物、p H值、电导率的变化及降水对污染物的清除作用。结果表明:无锡市梅雨期酸雨年平均p H值呈现逐年递增趋势。降水过程中,颗粒物质量浓度显著降低;气体浓度变化受其自身日变化及排放源影响大于雨水的清除作用;样品的p H值、K值每个过程变化并不一致,K值变化与颗粒物质量浓度变化大致保持一致。降水、风对颗粒物质量浓度影响大于对气体浓度的影响。长时间连续降水时,降水对颗粒污染物的清除存在极限。小时雨量在0~0.5 mm时,降水对颗粒物浓度做负清除,其值反而略有增加;小时雨量在0.6~5.0 mm时,降水对颗粒物质量浓度做正清除;小时雨量达到5.1 mm及以上时,对PM_(2.5)和PM_(2.5-10)做正清除,对PM_(10)做负清除。降水对SO_2有稀释清除作用;对NO_2的稀释作用取决于其开始浓度值;对CO、O_3的清除作用不显著。 相似文献
6.
为了解不同程度的降水对江浙沪地区大气PM_(2.5)的清除作用,搜集了2014—2016年该地区41个城市的降水和PM_(2.5)观测数据,通过对比2 a非降水和全时段PM_(2.5)平均浓度的差异,发现前者显著高于后者,说明降水对该地区PM_(2.5)具有清除作用。利用降水前与降水期间PM_(2.5)的浓度差异作为降水对PM_(2.5)的清除率,降水后与降水期间的浓度差异作为雨后浓度回升的增加率,分别研究了目标区域不同时期、不同降雨量以及不同降雨时长对PM_(2.5)的清除效果。结果显示:(1)与江浙沪南部地区不同的是,北部地区降水清除率与降水前浓度存在正相关,降水后浓度的增加与当地的排放量呈正相关。(2)当降水量为30 mm或者降水时长为36 h时,清除率增幅减缓,说明降水对PM_(2.5)的清除效率存在着阈值。 相似文献
7.
为研究雾和霾天气下VOCs时空变化特征,于2020年11月19日—2021年1月15日在江苏省东海国家气象观测站进行为期58 d的外场观测试验。利用自主研发的多旋翼无人机捕获2次辐射雾和2次霾天气过程,获得气温、气压、相对湿度、风向、风速、VOCs、O3等7种要素100多条垂直廓线。结果表明:时间上,霾过程夜间VOCs体积浓度(0.225~0.253 ppm(parts per million, 1 ppm=10-6))明显高于白天(0.191~0.205 ppm),雾形成前体积浓度(0.121~0.239 ppm)显著高于雾过程(0.056~0.209 ppm)。雾过程中VOCs体积浓度与雾强度变化相反,雾层高度与VOCs体积浓度剧烈变化高度一致,雾层(<200 m)中VOCs体积浓度(0.172~0.178 ppm)明显减小,显著低于雾形成前(0.195~0.240 ppm),雾层以上浓度变化大,雾结束后1 h内保持雾过程中分布特点。雾对逆温层中的水溶性污染物有清除作用,VOCs体积浓度和O3质量浓度均下降。 相似文献
8.
成核过程是地震机理研究的重要部分.通过岩石实验、高温高压和数值模拟认为,地震成核的临界尺度为大地震总破裂长度的十分之一,一般为10~20 km左右;地震成核时间从年到秒、甚至毫秒.本文利用山东省宁阳县华丰煤矿立体台网的岩爆观测,进行了公里尺度的破裂成核过程实验研究.通过对华丰煤矿1995年2月~1996年5月期间的地脉动记录和12000次小震记录资料的分析,计算了它们的地脉动、S波和P波振幅比以及S波波峰的到时差,得到ML=2.9矿震的成核时间为50天,成核临界尺度为5 km. 相似文献
9.
S. Lopez J. H. Topalian S. K. Mitra D. C. Montague 《Journal of Atmospheric Chemistry》1989,8(2):175-188
An experimental study of the scavenging of dichloromethane vapor by water drops falling at terminal velocity, has been carried out in the UCLA precipitation shaft, in order to test the predictions of theoretical washout models. Whereas good agreement between theory and experiment was found for drops of radius 0.332 mm, computed gas uptake rates for 1.253 and 2.21 mm radius drops were much slower than those measured, just as reported previously for the washout of both sulfur dioxide and acetaldehyde. An analysis shows that theory can be reconciled with all of the experimental data by replacing the compound specific aqueous phase Fickian molecular diffusion coefficient used in the theory, by an effective diffusivity, having a constant value, (3×10-4 cm2 s-1), independent of the physical and chemical nature of the absorbed species, for all drops of equivalent radii greater than 0.9 mm. 相似文献
10.
A garnet population in Yellowknife schist, Canada 总被引:6,自引:0,他引:6
R. KRETZ 《Journal of Metamorphic Geology》1993,11(1):101-120
Abstract Data are presented on a garnet population in a specimen of garnet-biotite-plagioclase-quartz schist from the cordierite zone of an Archaean thermal dome in the Southern Slave Province of the Canadian Shield. Garnet crystals are bounded by planar dodecahedral faces and by trapezohedral faces which on the 10-μm scale are corrugated. Crystal distribution, as revealed by dissection of a small cubic volume of rock, is random. The size distribution is normal, with a mean diameter of 0.81 mm and a standard deviation of 0.32 mm. In the largest crystal of the population (mean radius 0.83 mm), [Mn] = 100 Mn/(Fe + Mg + Mn + Ca) decreases from 14.5 at the centre to 7.5 and then increases in the outer margin to 8.5; [Fe] increases continuously from 67 at the centre to 77 at the surface; [Mg] increases from 12.5 to 13.5 and then falls sharply to 11; [Ca] remains unchanged at 4.0 and then drops to 3.3. Progressively smaller crystals have progressively lower [Mn] and higher [Fe] concentrations at their centres, while all crystals have the same margin composition. Growth vectors extending from given concentration contours to crystal surfaces are of equal length regardless of the size of the crystal in which the vector is located. A garnet-forming model is presented in which reaction was initiated by a rise in temperature. Nucleation sites were randomly selected. The nucleation rate increased with time and then declined. Crystal faces advanced at a constant linear rate, which implies an increase in volume proportional to surface area. Initially, the composition of garnet deposited on crystal surfaces was determined by van Laar equations of equilibrium, which demanded the withdrawal of Mn and Fe from within chlorite crystals. This transfer reaction was then accompanied by an ion exchange reaction which moved Mn and Fe to garnet surfaces from biotite, in exchange for Mg. The exchange reaction provides an explanation for the high overall concentration of Mn and Fe in garnet and for the observed Mn and Mg reversals in the margins of crystals. The increase of garnet volume in the garnet population is found to be parabolic, i.e. Vαα5. 相似文献