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11.
提出一种基于GPT2w模型化加权平均温度反演大气可降水量的方法,并分析附加系统偏差改正的模型化加权平均温度对可降水量的影响。结果表明,基于GPT2w模型化加权平均温度反演的大气可降水量的精度与基于Bevis公式计算的加权平均温度反演的大气可降水量的精度相当;对GPT2w模型化加权平均温度进行系统偏差改正后,大气可降水量的精度有一定改善,但改善率不到1%。 相似文献
12.
研究东日本地震、汶川地震和玉树地震震中及其附近区域在地震前后的水汽时间序列变化。首先分析震中MODIS水汽序列和震中附近探空站点水汽序列在地震前后的变化;然后基于GNSS ZTD与水汽之间的高相关性,以GNSS ZTD代替GNSS水汽,讨论震源区周围IGS站点的ZTD序列变化。研究发现,震后震中及其附近区域水汽值变化出现异常,且距离越近所受影响越大;水汽不断聚积,达到峰值后发生降水。 相似文献
13.
GPS静态精密单点定位算法精度分析 总被引:1,自引:0,他引:1
采用精密轨道和钟差,利用Bernese软件解算得到亚洲地区13个IGS跟踪站的站坐标、对流层ZTD和接收机钟差,将解算的结果与CODE发布的结果对比发现:静态PPP算法解算的N方向收敛精度明显优于E方向和U方向,4~6 h后,坐标偏差在1 cm左右;NEU RMS均值分别为0.45、0.29、0.69 cm,ZTD RMS均值为0.85 cm,接收机钟差RMS均值为0.14 ns。试验表明:精密单点定位算法具有较高的精度和可靠性,可为实际工程测量及相关地球物理信号研究提供理论依据。 相似文献
14.
长距离网络RTK是实现GPS/BDS高精度实时定位的主要手段之一,其核心是长距离参考站网GPS/BDS整周模糊度的快速准确确定。本文提出了一种长距离GPS/BDS参考站网载波相位整周模糊度解算方法,首先利用GPS双频观测数据计算和确定宽巷整周模糊度,同时利用BDS的B2、B3频率观测值确定超宽巷整周模糊度。然后建立GPS载波相位整周模糊度和大气延迟误差的参数估计模型,附加双差宽巷整周模糊度的约束,解算双差载波相位整周模糊度,并建立参考站网大气延迟误差的空间相关模型。根据B2、B3频率的超宽巷整周模糊度建立包含大气误差参数的载波相位整周模糊度解算模型,利用大气延迟误差空间相关模型约束BDS双差载波相位整周模糊度的解算。克服了传统的使用无电离层组合值解算整周模糊度的不利影响。采用实测长距离CORS网GPS、BDS多频观测数据进行算法验证,试验结果证明该方法可实现长距离参考站网GPS/BDS载波相位整周模糊度的准确固定。 相似文献
15.
在无气象数据的条件下,提出一种基于集合经验模态分解(EEMD)和季节性自回归移动平均模型(SARIMA)的对流层延迟(ZTD)预报新方法,并分别选取长春、上海、乌鲁木齐3个地区4个季节的ZTD数据进行预测分析。结果表明,基于EEMD-SARIMA的ZTD改正预报模型能够满足不同地区、不同季节下的ZTD估计需求,是一种高精度的ZTD预报方法。 相似文献
16.
采用线性回归和最小二乘法拟合建立无线电探空可降水量(RS-PWV)与GPS对流层延迟(GPS-ZTD)、地面温度及大气压之间的直接转换模型,并将直接转换模型得到的PWV分别与RS-PWV及GPS反演得到的可降水量(GPS-PWV)进行比较。结果表明,RS-PWV与GPS-ZTD之间存在良好的线性关系,相关系数达0.927 6;RS-PWV与4阶拟合温度和大气压呈现较好的相关性,相关系数分别为0.640 1和-0.626 3;基于ZTD的单阶单因子模型PWV与GPS-PWV的相关系数达到0.969 9;基于ZTD、温度及大气压的单阶多因子模型PWV比基于ZTD的单阶单因子模型PWV精度明显提高,RMS从4.3 mm提高到3.3 mm。 相似文献
17.
The diurnal cycle of the tropospheric zenith total delay (ZTD) is one of the most obvious signals for the various physical
processes relating to climate change on a short time scale. However, the observation of such ZTD oscillations on a global
scale with traditional techniques (e.g. radiosondes) is restricted due to limitations in spatial and temporal resolution.
Nowadays, the International GNSS Service (IGS) provides an important data source for investigating the diurnal and semidiurnal
cycles of ZTD and related climatic signals. In this paper, 10 years of ZTD data from 1997 to 2007 with a 2-hour temporal resolution
are derived from global positioning system (GPS) observations taken at 151 globally distributed IGS reference stations. These
time series are used to investigate diurnal and semidiurnal oscillations. Significant diurnal and semidiurnal oscillations
of ZTD are found for all GPS stations used in this study. The diurnal cycles (24 hours period) have amplitudes between 0.2
and 10.9 mm with an uncertainty of about 0.5 mm and the semidiurnal cycles (12 h period) have amplitudes between 0.1 and 4.3 mm
with an uncertainty of about 0.2 mm. The larger amplitudes of the diurnal and semidiurnal ZTD cycles are observed in the low-latitude
equatorial areas. The peak times of the diurnal cycles spread over the whole day, while the peak value of the semidiurnal
cycles occurs typically about local noon. These GPS-derived diurnal and semidiurnal ZTD signals are similar with the surface
pressure tides derived from surface synoptic pressure observations, indicating that atmospheric tides are the main driver
of the diurnal and semidiurnal ZTD variations. 相似文献
18.
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
19.
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
20.
We show that photochemical processes in the lower half of the troposphere are strongly affected by the presence of liquid water clouds. Especially CH2O, an important intermediate of CH4 (and of other hydrocarbon) oxidation, is subject to enhanced breakdown in the aqueous phase. This reduces the formation of HO
x
-radicals via photodissociation of CH2O in the gas phase. In the droplets, the hydrated form of CH2O, its oxidation product HCO2
–, and H2O2 recycle O2
– radicals which, in turn, react with ozone. We show that the latter reaction is a significant sink for O3. Further O3 concentrations are reduced as a result of decreased formation of O3 during periods with clouds. Additionally, NO
x
, which acts as a catalyst in the photochemical formation of O3, is depleted by clouds during the night via scavenging of N2O5. This significantly reduces NO
x
-concentrations during subsequent daylight hours, so that less NO
x
is available for O3 production. Clouds thus directly reduce the concentrations of O3, CH2O, NO
x
, and HO
x
. Indirectly, this also affects the budgets of other trace gases, such as H2O2, CO, and H2. 相似文献