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排序方式: 共有55条查询结果,搜索用时 187 毫秒
1.
执行S-57标准的若干问题处理 总被引:1,自引:0,他引:1
S-57作为一种国际标准,在各个国家的应用上根据实际情况有其局限性,ENC作为该标准的执行者,也受到了一定的限制,要减少这种限制,就需要了解并分析ENC生产中存在的问题。结合生产实践,总结了部分问题,以便进行分析研究。 相似文献
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运城盆地11 kaBP以来气候环境变迁与湖面波动 总被引:7,自引:0,他引:7
通过黄土区湖泊沉积研究来恢复古气候、古环境,是对黄土区古气候、古环境研究的补充和检验。通过山西运城盆地硝地湖泊沉积物的多环境代用指标分析,结合史料记载,探讨了该地区11kaBP以来古气候演化和湖面波动的历史。结果表明,该地区存在YD(Younger Dryas)事件,进入全新世后气候有显著的趋势,最高湿润度发生在7.88-5.15和5kaBP后,气候逐渐变干,湖面波动与气候波动相关,全新世早期湖面开始上升,湖泊扩张,5kaBP后湖泊萎缩,盐类结晶析出。 相似文献
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简述了原国家重力基本网(57网)的历史和技术要点,详细地分析了57网的各类误差和产生原因,提出了新、旧系统转换的方法。本文研究表明,57网基本点相对观测的实际精度约为±0.06mgal,仪器平均值误差为1.6×10~(-4)。基本点重力值含-13.56mgal的基准误差和1.9×10~(-4)的尺度差,并含有±0.1~0.2mgal的非线性系统误差。对基本点实行新、旧系统转换误差为±0.05mgal,基本不损失其观测精度。 相似文献
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The article aims at showing the differences in concentration of pollutants that are contained in the samples of fog and/or low cloud water in comparison with the water from rime. The results follow from the fog and rime measurements made at Mt. Mileovka (eské Stedohoí Mountains). They are compared with the results of other studies that also report the differences in fog and rime chemistry. 相似文献
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S.-U. Weber M. Grodzicki C. A. Geiger W. Lottermoser G. Tippelt G. J. Redhammer M. Bernroider G. Amthauer 《Physics and Chemistry of Minerals》2007,34(1):1-9
Three natural lawsonites from Syke Rock, Mendocino Co., Reed Ranch, Marin Co., and Blake Gardens, Sonoma Co., all from the Coast Range Region in California, were studied by 57Fe Mössbauer spectroscopy, electron microprobe analysis, and X-ray powder diffraction. The samples contain about 0.6, 1.0, and 1.4 wt% of total iron oxide, respectively. 57Fe Mössbauer spectra are consistent with the assumption that high-spin Fe3+ substitutes for Al in the octahedrally coordinated site. The Mössbauer spectrum of lawsonite from Syke Rock exhibits a second doublet with 57Fe hyperfine parameters typical for octahedrally coordinated high-spin Fe2+. Electronic structure calculations in the local spin density approximation yield quadrupole splittings for Fe3+ in quantitative agreement with experiment indicating, however, that substitution of Al by Fe3+ must be accompanied by local distortion around the octahedral site. Model calculations also reproduce the room temperature hyperfine parameters of ferrous high-spin iron assuming the substitution of Ca by Fe2+. However, it cannot be excluded that Fe2+ may occupy a more asymmetric site within the microstructural cavity occupied by Ca and a H2O molecule. 相似文献
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57Fe-Mössbauer spectra of eleven Fe-Mg-bearing staurolite samples, synthesized at 5, 20 and 25 kbar and 680°C, ranging in composition from xFe?=1.00 to xFe?=0.15, and of two Zn-Fe-bearing staurolite samples, synthesized at 20 kbar and 700°C with xFe?=0.10 and xFe?=0.32 were collected at room temperature. The spectra reveal that about 80% of Fetot (in case of Fe-Mg-bearing staurolite) and about 70% of Fetot (in case of Fe-Zn-bearing staurolite) are located as Fe2+ at the three subsites Fe1, Fe2 and Fe3 of the tetrahedral T2-site. The refinement of the spectra results in almost identical values for the isomer shift (IS) (±1.0 mm/s) but significantly different values for the quadropole splitting (QS) for the three subsites which is in accordance with the different distortions of these sites. About 8% of Fetot (in case of Fe-Mg-bearing staurolite) and 13% of Fetot (in case of Fe-Zn-bearing staurolite) are located as Fe2+ at the octahedral M4 site, while the remainder percents of Fetot indistinguishably occur as Fe2+ at the octahedral M1 and M2 sites of the kyanite-like part of the structure. Within the whole Fe-Mg-staurolite solid solution series the Mössbauer parameters QS of the sites M4 and (M1, M2) vary systematically with composition whereas IS remains constant. There is a high negative correlation of the total Mg-content with Fe-occupation of all the Fe-bearing sites indicating a continuous substitution of Fe2+ by Mg on all these sites. Synthetic Fe-staurolites show no increasing occupation of the octahedral sites by two-valent cations with pressure, as was assumed by several authors. 相似文献
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