全文获取类型
收费全文 | 585篇 |
免费 | 188篇 |
国内免费 | 322篇 |
专业分类
测绘学 | 86篇 |
大气科学 | 702篇 |
地球物理 | 43篇 |
地质学 | 75篇 |
海洋学 | 63篇 |
天文学 | 4篇 |
综合类 | 26篇 |
自然地理 | 96篇 |
出版年
2024年 | 6篇 |
2023年 | 10篇 |
2022年 | 24篇 |
2021年 | 33篇 |
2020年 | 23篇 |
2019年 | 21篇 |
2018年 | 35篇 |
2017年 | 28篇 |
2016年 | 43篇 |
2015年 | 37篇 |
2014年 | 57篇 |
2013年 | 58篇 |
2012年 | 54篇 |
2011年 | 61篇 |
2010年 | 46篇 |
2009年 | 61篇 |
2008年 | 43篇 |
2007年 | 33篇 |
2006年 | 57篇 |
2005年 | 55篇 |
2004年 | 37篇 |
2003年 | 48篇 |
2002年 | 22篇 |
2001年 | 17篇 |
2000年 | 33篇 |
1999年 | 16篇 |
1998年 | 24篇 |
1997年 | 11篇 |
1996年 | 11篇 |
1995年 | 14篇 |
1994年 | 15篇 |
1993年 | 11篇 |
1992年 | 8篇 |
1991年 | 6篇 |
1990年 | 6篇 |
1989年 | 6篇 |
1988年 | 5篇 |
1986年 | 6篇 |
1985年 | 6篇 |
1984年 | 1篇 |
1983年 | 1篇 |
1982年 | 3篇 |
1980年 | 1篇 |
1978年 | 1篇 |
1977年 | 1篇 |
排序方式: 共有1095条查询结果,搜索用时 163 毫秒
101.
利用OMI卫星资料2006—2017年的483.5 nm波长的气溶胶柱单次散射反照率日均数据,分析了整层大气气溶胶单次散射反照率在长三角地区的时空分布特征,特别是其年际、月、季节变化特征.长江三角洲地区的大气气溶胶柱单次散射反照率越靠近海洋越大,而越靠近内陆越小.日均气溶胶柱单次散射反照率在0.881~0.971范围内变化,多年的平均值为0.939±0.024,最大分布概率出现在0.965~0.970区间,其值约为25%.长三角地区大气气溶胶柱单次散射反照率的年平均值集中于0.938~0.940之间,年际变化很小,变化值小于1%;月均柱单次散射反照率在6、8、9月有最大值,其值为0.968,而在2月有最小值,其值为0.915;季节平均单次散射反照率在夏季最大,其值为0.968,而在冬季最小,其值为0.919. 相似文献
102.
Hajime Fukushima Akiko Higurashi Yasushi Mitomi Teruyuki Nakajima Toshimitsu Noguchi Toshio Tanaka Mitsuhiro Toratani 《Journal of Oceanography》1998,54(5):417-430
This paper first describes the atmospheric correction algorithm for OCTS visible band data used at NASDA/EOC. Sharing a basic
structure with Gordon and Wang’s Sea WiFS algorithm, it uses 10 candidate aerosol models including the “Asian dust model”
introduced in consideration of the unique feature of aerosols over the east Asian waters. Based on the observations at 670
and 865 nm bands, the algorithm selects a pair of aerosol models that account best for the observed spectral reflectances,
and synthesizes the aerosol reflectance used for the atmospheric correction. Two different schemes for determining the value
of the parameter for the aerosol model selection are presented and their anticipated estimation error is analyzed in terms
of retrieved water reflectance at 443 nm. The results of our numerical simulation show that the standard deviation of the
estimation error of the “weighted average” scheme is mostly within the permissible level of ±0.002, reducing the error by
18% on average compared to the “simple average” scheme. The paper further discusses the expected error under the old CZCS-type
atmospheric correction, which assumes constant aerosol optical properties throughout the given image. Although our algorithm
has a better performance than the CZCS algorithm, further analysis shows that the error induced by the assumption taken in
the algorithm that the water-leaving radiance at 670 nm band is negligibly small may be large in high pigment concentration
waters, indicating the necessity for future improvements. 相似文献
103.
为了解香河地区气溶胶尺度谱的基本特征,自2012年5月起,利用扫描电迁移率粒径谱仪(SMPS)对河北香河地区的亚微米(13.8~723.4 nm)气溶胶尺度谱分布进行了近2 a的测量。基于该数据集,分析了气溶胶尺度谱的季节变化和日变化特征及气象要素对气溶胶浓度的影响。结果发现,观测期间埃根核模态(20.0~100.0 nm)、积聚模态(100.0~723.4 nm),以及总的气溶胶数浓度、表面积浓度和体积浓度均值分别为7.0×103cm~(-3)、7.5×103cm~(-3)、14.9×103cm~(-3)、1125μm2·cm~(-3)和50μm~3·cm~(-3)。香河地区积聚模态的粒子数浓度接近华北地区其他污染测站的结果,但高于发达国家的测值。冬季气溶胶的平均浓度最高(18.1×10~3cm~(-3)),而春季最低(12.3×10~3cm~(-3))。不同季节,气溶胶的数谱分布主要为单峰分布,平均峰值直径约为105 nm。气溶胶浓度的日变化受机动车排放的影响显著,存在早晚两个高值中心,分别出现在早上的06:00—09:00和晚上的19:00—21:00。风速、风向对气溶胶数浓度的影响较大,低风速(2 m/s)和南风条件,尤其是吹西南风时,气溶胶浓度的增加显著。 相似文献
104.
The halogen ions Br- and Cl- together with NO3
-, SO4
=, MSA- (methane sulfonate), Na+ and NH4
+ were analysed by ion chromatography in extracts of more than 800 aerosol cellulose filter samples taken at Ny Ålesund, Svalbard (79°N, 12°E) in spring 1996 (March 27 - May 16) within the European Union project ARCTOC (Arctic Tropospheric Ozone Chemistry). Anticorrelated variations between f-Br (filterable bromine, i.e. water soluble bromine species that can be collected by aerosol filters) and ozone within the arctic troposphere were evaluated at a resolution of 1 or 2 hours for periods with depleted ozone and 4 hours at normal ozone. A mean f-Br concentration of 11 ng m-3 (0.14 nmol m-3) was observed for the whole campaign, while maximum concentrations of 80 ng m-3 (1 nmol m-3) were detected during two total O3-depletion events (O3 drop to mixing ratios below the detection limit of < 2 ppb). Anticorrelation between f-Br and O3 was also seen during minor O3-depletion episodes (sudden drop in O3 by at least 10 ppb, but O3 still exceeding the detection limit) and even for ozone variations near its background level (40-50 ppb). A time lag of about 10 hours between the change of ozone and of f-Br concentrations could only be found during a total ozone depletion event, when f-Br reached its maximum values several hours after ozone was totally destroyed. Bromine oxide (BrO) concentrations, measured by DOAS (Differential Optical Absorption Spectroscopy), and f-Br showed a coincident variability during almost the entire campaign (except in the case of total O3-loss). Frequently enhanced anthropogenic nitrate and sulphate concentrations were observed during O3-depletion periods. At O3 concentrations < 10 ppb sulphate and nitrate exceed their typical mean level by 54% and 77%, respectively. This may indicate a possible connection between acidity and halogen release. 相似文献
105.
G. P. Ayers R. W. Gillett J. M Cainey A. L. Dick 《Journal of Atmospheric Chemistry》1999,33(3):299-319
Datasets on aerosol composition in Southern Ocean air at Cape Grim and Macquarie Island, and rainwater composition at Cape Grim, have been analysed for sea-salt components in order to test the validity of the multiphase autocatalytic halogen activation process proposed initially by Sander and Crutzen (1996) and developed fully for clean marine air by Vogt et al. (1996). Four distinct datasets from the two locations were analysed. All four datasets provided consistent evidence in support of three predictions of the autocatalytic model: (1) overall Cl- deficits in sea-salt aerosol were small, difficult to quantify against analytical uncertainty and at most a few percent; (2) Br- deficits were large, averaging –30% to –50% on an annual basis, with strong seasonality ranging from about –10% in some winter samples to –80% or more in some summer samples; and (3) the Br- and Cl- deficits were clearly linked to the availability of strong, S-acidity in the aerosol, confirming the importance of acid catalysis to the dehalogenation process. 相似文献
106.
107.
INTRODUCTIONTheattentiontothestudyofmetalsinthemarineaerosolparticulatesisincreasingduetotheirenvironmentalecologicaleffectsandcontributiontothebiogeochemicalcycle.Intheaspectofenvironmentalecologicaleffects,first,onthesideofclimate,aerosolswithmetalscanactascloudcondensationoricenuclei,absorbandscattersolarradiation,andaffecttheradiationbudgetontheearth.Therelativelyhighironcontent(5%)ofthedustcanabsorbtheshortwavelengthradiationefficiently.Second,onthesideofecologicaleffects,di~lvedAlse… 相似文献
108.
I~IOWDuceetal.(1980)calculatedthattheair-seaexchangeprocesscouldsupply80%--90%ofthediforedironinputtothephotcrzoneoftheSargassoAsfromairand16%--76%tothecentralNorthPacific.CuisessentialtotheTnarineorganisms,butexcessiveCuistoxictOtheOrganisms.CdandPh... 相似文献
109.
The photochemical oxidation of SO2 in the presence of NO and C3H6 was studied in a 18.2 liter pyrex reactor. When light intensity, irradiation time and SO2 concentration were constant, SO4
2- concentration, derived from the total volume of aerosol produced, peaked when [C3H6]/[NO] was approximately 6.0. Another increase im SO4
2- formation was reached at very high ratios (>50). The experimental observations are consistent with the two SO2 oxidation mechanisms. At low [C3H6]/[NO] ratios, the processes proceed via the HO–SO2 reaction, while at high ratios the O3–C3H6 adduct is assumed to oxidize SO2 to produce SO4
2- aerosols. 相似文献
110.
大气气溶胶中若干有机物的含量和季节变化 总被引:4,自引:2,他引:2
研究、探讨青岛近岸大气气溶胶中多芳烃类化合物的浓度水平、变化特征及影响因素。用高效液相色谱荧光检测法分析了青岛近岸大气气溶胶中的多环芳烃(PAHs)的含量水平,共检出13种多环芳烃化合物。结果表明该类化合物总量(∑PAHs)具有明显的季节特征,呈现春季<秋季<冬季的特征,人类活动可能是其主要来源。 相似文献