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1.
2.
Daily zenith scattered light intensity observations were carried out in the morning twilight hours using home-made UV-visible
spectrometer over the tropical station Pune (18‡31′, 73‡51′) for the years 2000–2003. These observations are obtained in the
spectral range 462–498 nm for the solar zenith angles (SZAs) varying from 87‡ to 91.5‡. An algorithm has been developed to
retrieve vertical profiles of ozone (O3) and nitrogen dioxide (NO2) from ground-based measurements using the Chahine iteration method. This retrieval method has been checked using measured
and recalculated slant column densities (SCDs) and they are found to be well matching. O3 and NO2 vertical profiles have been retrieved using a set of their air mass factors (AMFs) and SCDs measured over a range of 87–91.5‡
SZA during the morning. The vertical profiles obtained by this method are compared with Umkehr profiles and ozonesondes and
they are found to be in good agreement. The bulk of the column density is found near layer 20–25 km. Daily total column densities
(TCDs) of O3 and NO2 along with their stratospheric and tropospheric counterparts are derived using their vertical profiles for the period 2000–2003.
The total column, stratospheric column and tropospheric column amounts of both trace gases are found to be maximum in summer
and minimum in the winter season. Increasing trend is found in column density of NO2 in stratospheric, tropospheric and surface layers, but no trend is observed in O3 columns for above layers during the period 2000–2003 相似文献
3.
为解决城市边界层中大气O3浓度的预报问题,选用一种简明有效的光化学反应方案建立光化学模式, 并与大气平流扩散的箱格预报模型进行了嵌套,从而将大气化学过程引入到城市空气污染数值预报系统 (CAPPS) 中。同时,根据实际需要研究了VOC (Volatile Organic Compounds) 浓度及NOx源排放量等参数缺测时,根据前期监测浓度采用遗传算法反演未知参数的具体方法。利用2001年9月8~17日在北京舞蹈学院监测的O3、NOx资料及相应的气象数据,用改进后的CAPPS模式进行了单箱预报试验。预报试验结果表明,嵌套后的模式对O3浓度的变化具备一定的预报能力。 相似文献
4.
《Comptes Rendus Geoscience》2018,350(7):435-441
Many observers and commentators have used the case of ozone science and politics as a role model for climate science and politics. Two crucial assumptions underpin this view: (1) that science drives policymaking, and (2) that a unified, international science assessment is essential to provide “one voice” of science that speaks to policymakers. I will argue that these assumptions are theoretically problematic and empirically questionable. We should realize that both cases, ozone and climate, are profoundly different and only have superficial similarities. Ozone science developed late, but efforts to protect the ozone layer happened swiftly. The relation between carbon dioxide and climate change has been studied for many decades, but efforts to control global warming have failed so far. I will discuss the linear model of the science-policy relationship and use the typology of tame and wicked problems to explain this stark difference. 相似文献
5.
基于WACCM+DART的临近空间SABER和MLS臭氧观测同化试验研究 总被引:1,自引:0,他引:1
本研究在WACCM+DART(Whole Atmosphere Community Climate Model,Data Assimilation Research Test-Bed)临近空间资料同化预报系统中加入SABER(Sounding of the Atmosphere using Broadband Emission Radiometry)和MLS(Microwave Limb Sounder)臭氧观测同化接口,并以2016年2月一次平流层爆发性增温(SSW)过程为模拟个例进行了SABER和MLS臭氧观测同化试验,得出以下结论:同化SABER和MLS臭氧体积浓度观测得出的WACCM+DART臭氧分析场能够较真实反映SSW期间北极上空平流层臭氧廓线随时间的演变特征,且与ERA5(Fifth Generation of ECMWF Reanalyses)再分析资料描述的臭氧变化特征具有很好的一致性;基于SABER和MLS臭氧观测的WACCM臭氧6 h预报检验表明同化臭氧观测对臭氧分析和预报误差的改善效果主要体现在南半球高纬平流层和北半球中高纬平流层中上层-中间层底部;基于ERA5再分析资料的WACCM+DART分析场检验表明同化SABER和MLS臭氧体积浓度资料可在提高北半球高纬地区上平流层-中间层底部臭氧场分析质量的同时减小该地区上平流层-中间层底部温度场和中间层底部纬向风场的分析误差;基于MLS臭氧资料的臭氧中期预报检验表明相对控制试验同化SABER和MLS臭氧体积浓度资料能更好改善0~5 d下平流层和中间层底部臭氧的预报效果。 相似文献
6.
疫情期间全球各地一次排放大幅削减,而臭氧等二次污染的响应则存在着区域间差异.结合地面和卫星观测发现,同在氮氧化物大幅下降的情况下,臭氧在东亚和欧洲呈现出可达14ppb的上升信号,而北美则下降为主(约2-4ppb).我们结合气象分析和臭氧敏感性进一步讨论了臭氧响应差异性的原因,一方面受臭氧与前体物间关系的影响;另一方面来... 相似文献
7.
文章研究了臭氧及臭氧类高级氧化技术(AOPs-O3)在不同pH条件下降解甲基对硫磷(MP)的效能。结果表明,在pH 3~10的条件下(反应过程控制pH),单独臭氧化5min即可完全降解MP,但不同pH下化学耗氧量(COD)和有机磷的释放率差异明显。在pH为3.3,7.5和9.4的条件下单独臭氧30min后COD的去除率分别为55.17%,89.64%和93.10%,有机磷的释放率分别为16.33%,95.00%和99.99%。考虑酸性条件下可以规避碳酸盐的负面影响(特别是高浓度废水),利用O3/H2O2/Ti(IV)在pH 3.3条件下处理MP溶液,COD去除率和有机磷释放率分别达到89.64%和81.57%。相对法计算求得MP与O3和羟基自由基(·OH)的速率常数分别为31.98L·(mol·s)-1和7.488×109 L·(mol·s)-1。活性污泥法的测试结果表明,MP经O3/Ti(IV)/H2O2(pH=3.3)和O3(pH=9.4)可提升含MP废水的可生化性,但与培养液体系相比仍具有一定的毒性。 相似文献
8.
Simultaneous ozone measurements were made at a rural site, 25 km SSW of the city of Jerusalem, and in the center of the city during a period of 28 months. The ozone data were supplemented by SO2, NO/NO
x
,and meteorological measurements at both sites. Elevated ozone concentrations were recorded at the rural site, mostly during the spring months (May and June) during which the monthly averages and the monthly averages of the daily 30 min maximum levels equalled those measured in the city. During the summer months, both average and peak levels were lower at the rural site by 20 and 35 ppb. The increased ozone levels at the rural site were accompanied by a parallel increase of SO2 and NO
x
,suggesting hat the excess ozone at the rural site is a result of a transformation during transport of air pollutants from coastal sources. 相似文献
9.
The response of tropospheric ozone to a change in solar UV penetration due to perturbation on column ozone depends critically on the tropospheric NO
x
(NO+NO2) concentration. At high NO
x
or a polluted area where there is net ozone production, a decrease in column ozone will increase the solar UV penetration to the troposphere and thus increase the tropospheric ozone concentration. However, the opposite will occur, for example, at a remote oceanic area where NO
x
is so low that there is net ozone destruction. This finding may have important implication on the interpretation of the long term trend of tropospheric ozone. A change in column ozone will also induce change in tropospheric OH, HO2, and H2O2 concentrations which are major oxidants in the troposphere. Thus, the oxidation capacity and, in turn, the abundances of many reduced gases will be perturbed. Our model calculations show that the change in OH, HO2, and H2O2 concentrations are essentially independent of the NO
x
concentration. 相似文献
10.
Ronald G. Prinn 《Journal of Atmospheric Chemistry》1988,6(3):281-298
An examination of typical tropospheric ozone variability on daily, monthly, annual and interannual timescales and instrumental precision indicates that the current ozonesonde network is insufficient to detect a trend in tropospheric ozone of 1% per year at the 2 level even at stations with records a decade in length. From a trend prediction analysis we conclude that in order to detect a 1% per year trend in a decade or less it will be necessary to decrease the time between observations from its present value of 3–7 days to 1 day or less. The spatial distribution of the current ozonesonde stations is also inadequate for determining the global climatology of ozone. We present a quantitative theory taking into account photochemistry, surface deposition, and wind climatology to define the effectively sampled region for an observing station which, used in conjunction with the instrumental precision and the above prediction analysis, forms the basis for defining a suitable global network for determining regional and global ozone climatology and trends. At least a doubling of the present number of stations is necessary, and the oceans, most of Asia, Africa, and South America are areas where more stations are most needed. Differential absorption lidar ozone instruments have the potential for far more frequent measurements of ozone vertical profiles and hence potentially more accurate climatology and trend determinations than feasible with ozonesondes but may produce a (fair weather) biased data set above the cloud base. A strategy for cloudy regions in which either each station utilizes both lidars and sondes or each station is in fact a doublet comprised of a near-sea-level lidar and a proximal-mountain-top lidar could serve to minimize this bias. 相似文献