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81.
82.
Jean de la Paix Mupenzi Lanhai Li Jiwen Ge Achal Varenyam Gabriel Habiyaremye Nzayisenga Theoneste Kamanzi Emmanuel 《地学前缘(英文版)》2011,2(4):599-607
This study has focused on the processes of soil degradation and chemical element concentration
in tea-growing regions of Rwanda, Africa. Soil degradation accelerated by erosion is caused not only
by topography but also by human activities. This soil degradation involves both the physical loss and
reduction in the amount of topsoil associated with nutrient decline. Soil samples were collected from
eleven tropical zones in Rwanda and from variable depth within each collecting site. Of these, Samples
from three locations in each zone were analyzed in the laboratory, with the result that the pH of all soil
samples is shown to be less than 5 (pH < 5) with a general average of 4.4. The elements such as iron (Fe),
copper (Cu), manganese (Mn), and zinc (Zn) are present in high concentration levels. In contrast calcium
(Ca) and sodium (Na) are present at low-level concentrations and carbon (C) was found in minimal concentrations. In addition, elements derived from fertilizers, such as nitrogen (N), phosphorous (P), and
potassium (K) which is also from minerals such as feldspar, are also present in low-level concentrations.
The results indicate that the soil in certain Rwandan tea plantations is acidic and that this level of pH may
help explain, in addition to natural factors, the deficiency of some elements such as Ca, Mg, P and N. The
use of chemical fertilizers, land use system and the location of fields relative to household plots are also
considered to help explain why tea plantation soils are typically degraded. 相似文献
83.
Brbel Hnisch Torsten Bickert N. Gary Hemming 《Earth and Planetary Science Letters》2008,272(1-2):309-318
Here we present the first species-specific study of boron isotopes in the epibenthic foraminifer species Cibicidoides wuellerstorfi. Coretop samples from a water depth profile from 1000 to 4500 m on the northern flank of the Walvis Ridge are 4.4‰ lower than the values expected, based on calculations of the δ11Bborate of ambient seawater. Similar values for this foraminifer species are presented from ODP site 668B at the Sierra Leone Rise, in the equatorial Atlantic. The consistency between data of the same species suggests the offsets are primary, rather than diagenetic. Glacial C. wuellerstorfi from ODP 668B and Walvis Ridge have boron isotope compositions only slightly different to interglacial samples, that is no larger than + 0.10 pH units, or + 23 µmol kg− 1 in [CO32−] above the reconstructed glacial lysocline, and − 0.07 pH units, or − 14 µmol kg− 1 in [CO32−] below. We use these results to suggest that glacial deep water pH in the Atlantic was similar to interglacial pH. The new data resolve the inconsistency between the previously reported high bottom water pH and the lack of significant carbonate preservation of the glacial deep ocean. 相似文献
84.
天山哈密庙尔沟平顶冰川和奎屯河哈希勒根51号冰川成冰带与雪层pH值和电导率对比研究 总被引:1,自引:0,他引:1
对天山哈密庙尔沟平顶冰川和奎屯河哈希勒根51号冰川的雪层剖面及雪坑中pH值和电导率的变化特征进行了初步研究.结果表明:哈密庙尔沟平顶冰川以渗浸-冻结成冰作用为主,一年成冰,成冰带由消融带和渗浸-冻结带组成,渗浸-冻结带的垂直高度在60 m左右或者更大一点;奎屯河哈希勒根51号冰川的成冰作用以暖型为主,成冰带由消融带、渗浸-冻结带和渗浸带组成,渗浸-冻结带的垂直高度不大于70 m.雪坑中pH值和电导率的较高值一般出现在冰片和污化层附近,这与冰的阻碍、引起可溶性离子在冰面上部的高浓度值和可溶性离子的淋溶过程与污化物的迁移过程密切联系直接相关.哈密庙尔沟平顶冰川雪坑中pH值和电导率之间的相关性异于奎屯河哈希勒根51号冰川,由于雪坑的资料有限,有待进一步的深入研究. 相似文献
85.
α-1,4-葡聚糖裂解酶的动力学性质研究 总被引:1,自引:0,他引:1
Sun Xue 《中国海洋大学学报(自然科学版)》2000,30(Z1):230-236
红藻中的α-1,4-葡聚糖裂解酶是红藻淀粉的降解酶,除了 红藻淀粉外,它还可以作用于多种底物。文中分别以PNPG和可溶性淀粉作底物,以龙须菜的 几个品系作为材料,研究了该酶促反应的动力学方面的性质。以 PNPG作为底物,该酶在60m in内酶促反应速度与保温时间成线性关系;在野生型龙须菜品系中该酶的最适反应温度是50 ℃,在两种突变型品系中是40℃;最适pH范围在4.4~5.5;底物浓度是4mmol/L时达到最大反 应速度;葡萄糖对该酶促反应有明显的抑制作用。以可溶性淀粉作为底物,在反应60 min内 酶反应速度与保温时间成线性关系;最适反应温度为50℃;最适pH范围在5.0~5.8;底物浓 度是8mg/mL时达到最大反应速度;葡萄糖对可溶性淀粉的抑制作用比对PNPG的弱。 相似文献
86.
Peter G. Brewer Edward T. Peltzer Gernot Friederich Izuo Aya Kenji Yamane 《Marine Chemistry》2000,72(2-4)
We have carried out a series of in situ experiments to investigate the formation of a CO2 hydrate (CO2:5.75 H2O) for the purpose of evaluating scenarios for ocean fossil fuel CO2 disposal with a solid hydrate as the sequestered form. The experiments were carried out with a remotely operated vehicle in Monterey Bay at a depth of 619 m. pH measurements made in close proximity to the hydrate–seawater interface showed a wide range of values, depending upon the method of injection and the surface area of the hydrate formed. Rapid injection of liquid CO2 into an inverted beaker to form a flocculant mass of hydrate resulted in pH initially as low as 4.5 within a few centimeters of the interface, decaying slowly over 1–2 h towards normal seawater values as dense CO2 rich brine drained from the hydrate mass. In a second experiment, slower injection of the liquid CO2 to produce a simple two-layer system with a near planar interface of liquid CO2 with a thin hydrate film yielded pH values indistinguishable from the in situ ocean background level of 7.6. Both field and laboratory results now show that the dissolution rate of a mass of CO2 hydrate in seawater is slow but finite. 相似文献
87.
KANG Shi chang QIN Da he YAO Tan dong PAUL A. Mayewski SALLIE Whitlow 《中国地理科学(英文版)》2000,10(3):218-225
Investigations of atmospheric composition in the Himalayas has been limited in both temporal and spatial scales, mainly due to difficult logistics. Ideal sites for monitoring atmospheric composition and its evolution should be free from local pollution and representative of the remote troposphere (HUEBERT et al., 1980). As the Himalayas are far removed from highly industrialized regions they provide suitable locations to monitor the chemistry of the remote troposphere and to study the evolu… 相似文献
88.
89.
三疣梭子蟹消化酶的初步研究 总被引:9,自引:1,他引:8
开发研制配合饲料,以酶学分析方法研究了温度、pH对三疣梭子蟹(Portunus trituberculatus)中肠腺3种主要消化酶(蛋白酶、淀粉酶和纤维素酶)活性的影响及消化酶(蛋白酶、胰蛋白酶、胰凝乳蛋白酶、羧肽酶A、羧肽酶B、淀粉酶、脂肪酶和纤维素酶)在胃、中肠腺、肠道中的活性分布。结果表明:蛋白酶、淀粉酶、纤维素酶的最适温度分别为55℃,55℃,65℃;蛋白酶、淀粉酶、纤维素酶的最适pH分别为7~8,7.5,4.8;蛋白酶、淀粉酶、纤维素酶在短时间内有很高的热稳定性及很广的酸碱稳定性范围。蛋白酶、胰蛋白酶、羧肽酶A、羧肽酶B活性均以中肠腺最高,胃和肠道中没有测出胰凝乳蛋白酶活性;淀粉酶活性在胃、中肠腺、肠道中差别不大;纤维素酶和脂肪酶活性在胃和肠道高于中肠腺。 相似文献
90.
采用(斜长石+黑云母+石英)这三种单矿物组合与1mol/L NaCl或0.5mol/L NaCl 0.5mol/L NaHCO3溶液在450-250℃和50MPa条件下反应7d。实验表明,反应后流体pH值发生了变化,NaCl介质向酸性变化,N aCl NaHCO3介质向中性转化。溶液中K,Ca,Mg,Fe和Au量也随之发生变化。矿物表面发生溶解和离子置换等反应。斜长石表面形成钠长石反应边,黑云母变色,石英重结晶,反应器皿金管中的金被溶解后在金管壁和黑云母表面重结晶,黑云母周边出现红色Fe2O3,在450℃的NaCl介质中,金含量可达1070μg/g,但随温度下降迅速减低,在NaCl NaHCO3介质中,金含量较低,显著,金的活化迁移和富集与Cl,pH,Fe^3 /Fe^2 密切相关,这中金起到示踪作用,显示出金在水/岩反应中的原电池效应。 相似文献