全文获取类型
收费全文 | 347篇 |
免费 | 56篇 |
国内免费 | 165篇 |
专业分类
大气科学 | 71篇 |
地球物理 | 50篇 |
地质学 | 271篇 |
海洋学 | 103篇 |
天文学 | 2篇 |
综合类 | 23篇 |
自然地理 | 48篇 |
出版年
2024年 | 3篇 |
2023年 | 1篇 |
2022年 | 10篇 |
2021年 | 14篇 |
2020年 | 16篇 |
2019年 | 18篇 |
2018年 | 13篇 |
2017年 | 11篇 |
2016年 | 18篇 |
2015年 | 21篇 |
2014年 | 36篇 |
2013年 | 26篇 |
2012年 | 14篇 |
2011年 | 27篇 |
2010年 | 24篇 |
2009年 | 31篇 |
2008年 | 25篇 |
2007年 | 23篇 |
2006年 | 27篇 |
2005年 | 30篇 |
2004年 | 24篇 |
2003年 | 21篇 |
2002年 | 12篇 |
2001年 | 12篇 |
2000年 | 18篇 |
1999年 | 12篇 |
1998年 | 12篇 |
1997年 | 9篇 |
1996年 | 7篇 |
1995年 | 5篇 |
1994年 | 8篇 |
1993年 | 5篇 |
1992年 | 9篇 |
1991年 | 7篇 |
1990年 | 5篇 |
1989年 | 3篇 |
1988年 | 3篇 |
1987年 | 2篇 |
1986年 | 1篇 |
1985年 | 1篇 |
1984年 | 2篇 |
1983年 | 1篇 |
1982年 | 1篇 |
排序方式: 共有568条查询结果,搜索用时 31 毫秒
41.
42.
Annual wet deposition of excess sulfate at Macquarie Island has been estimated from 5 months of rainwater composition data covering the Austral summer of 1985/86. The resulting figure of 2.1±0.6 mmol/m2/yr is at the low end of previous estimates of maritime excess sulfate deposition by precipitation. Within estimated uncertainty limits this figure is consistent with the DMS emission flux which would be predicted for latitude 50°–60° S, based solely on available Northern Hemispheric DMS measurements.Temporarily at the International Meteorological Institute, Stockholm University, S-106 91, Stockholm, Sweden. 相似文献
43.
Nitrogen and sulfur species in Antarctic aerosols at Mawson,Palmer Station,and Marsh (King George Island) 总被引:4,自引:0,他引:4
D. L. Savoie J. M. Prospero R. J. Larsen F. Huang M. A. Izaguirre T. Huang T. H. Snowdon L. Custals C. G. Sanderson 《Journal of Atmospheric Chemistry》1993,17(2):95-122
High volume bulk aerosol samples were collected continuously at three Antarctic sites: Mawson (67.60° S, 62.50° E) from 20 February 1987 to 6 January 1992; Palmer Station (64.77° S, 64.06° W) from 3 April 1990 to 15 June 1991; and Marsh (62.18° S, 58.30° W) from 28 March 1990, to 1 May 1991. All samples were analyzed for Na+, SO
4
2–
, NO
3
–
, methanesulfonate (MSA), NH
4
+
,210Pb, and7Be. At Mawson for which we have a multiple year data set, the annual mean concentration of each species sometimes vary significantly from one year to the next: Na+, 68–151 ng m–3; NO
3
–
, 25–30 ng m–3; nss SO
4
2–
, 81–97 ng m–3; MSA, 19–28 ng m–3; NH
4
+
, 16–21 ng m–3;210Pb, 0.75–0.86 fCi m–3. Results from multiple variable regression of non-sea-salt (nss) SO
4
2–
with MSA and NO
3
–
as the independent variables indicates that, at Mawson, the nss SO
4
2–
/MSA ratio resulting from the oxidation of dimethylsulfide (DMS) is 2.80±0.13, about 13% lower than our earlier estimate (3.22) that was based on 2.5 years of data. A similar analysis indicates that the ratio at Palmer is about 40% lower, 1.71±0.10, and more comparable to previous results over the southern oceans. These results when combined with previously published data suggest that the differences in the ratio may reflect a more rapid loss of MSA relative to nss SO
4
2–
during transport over Antarctica from the oceanic source region. The mean210Pb concentrations at Palmer and Marsh and the mean NO
3
–
concentration at Palmer are about a factor of two lower than those at Mawson. The210Pb distributions are consistent with a210Pb minimum in the marine boundary layer in the region of 40°–60° S. These features and the similar seasonalities of NO
3
–
and210Pb at Mawson support the conclusion that the primary source regions for NO
3
–
are continental. In contrast, the mean concentrations of MSA, nss SO
4
2–
, and NH
4
+
at Palmer are all higher than those at Mawson: MSA by a factor of 2; nss SO
4
2–
by 10%; and NH
4
+
by more than 50%. However, the factor differences exhibit substantial seasonal variability; the largest differences generally occur during the austral summer when the concentrations of most of the species are highest. NH
4
+
/(nss SO
4
2–
+MSA) equivalent ratios indicate that NH3 neutralizes about 60% of the sulfur acids during December at both Mawson and Palmer, but only about 30% at Mawson during February and March. 相似文献
44.
Numerical study of the oxidation process of dimethylsulfide in the marine atmosphere 总被引:1,自引:0,他引:1
A box model, involving simple heterogeneous reaction processes associated with the production of non-sea-salt sulfate (nss-SO
4
2–
) particles, is used to investigate the oxidation processes of dimethylsulfide (DMS or CH3SCH3) in the marine atmosphere. The model is applied to chemical reactions in the atmospheric surface mixing layer, at intervals of 15 degrees latitude between 60° N and 60° S. Given that the addition reaction of the hydroxyl radical (OH) to the sulfur atom in the DMS molecule is faster at lower temperature than at higher temperature and that it is the predominant pathway for the production of methanesulfonic acid (MSA or CH3SO3H), the results can well explain both the increasing tendency of the molar ratio of MSA to nss-SO
4
2–
toward higher latitudes and the uniform distribution with latitude of sulfur dioxide (SO2). The predicted production rate of MSA increases with increasing latitude due to the elevated rate constant of the addition reaction at lower temperature. Since latitudinal distributions of OH concentration and DMS reaction rate with OH are opposite, a uniform production rate of SO2 is realized over the globe. The primary sink of DMS in unpolluted air is caused by the reaction with OH. Reaction of DMS with the nitrate radical (NO3) also reduces DMS concentration but it is less important compared with that of OH. Concentrations of SO2, MSA, and nss-SO
4
2–
are almost independent of NO
x
concentration and radiation field. If dimethylsulfoxide (DMSO or CH3S(O)CH3) is produced by the addition reaction and further converted to sulfuric acid (H2SO4) in an aqueous solution of cloud droplets, the oxidation process of DMSO might be important for the production of aerosol particles containing nss-SO
4
2–
at high latitudes. 相似文献
45.
The biogeochemical sulfur cycle in the marine boundary layer over the Northeast Pacific Ocean 总被引:1,自引:0,他引:1
T. S. Bates J. E. Johnson P. K. Quinn P. D. Goldan W. C. Kuster D. C. Covert C. J. Hahn 《Journal of Atmospheric Chemistry》1990,10(1):59-81
The major components of the marine boundary layer biogeochemical sulfur cycle were measured simultaneously onshore and off the coast of Washington State, U.S.A. during May 1987. Seawater dimethylsulfide (DMS) concentrations on the continental shelf were strongly influenced by coastal upwelling. Concentration further offshore were typical of summer values (2.2 nmol/L) at this latitude. Although seawater DMS concentrations were high on the biologically productive continental shelf (2–12 nmol/L), this region had no measurable effect on atmospheric DMS concentrations. Atmospheric DMS concentrations (0.1–12 nmol/m3), however, were extremely dependent upon wind speed and boundary layer height. Although there appeared to be an appreciable input of non-sea-salt sulfate to the marine boundary layer from the free troposphere, the local flux of DMS from the ocean to the atmosphere was sufficient to balance the remainder of the sulfur budget. 相似文献
46.
Thomas Striebel Wolfgang Schäfer Stefan Peiffer 《Aquatic Sciences - Research Across Boundaries》1991,53(4):346-366
A field study on the geochemical properties of a chemically-stressed limnic environment was performed in Lake Silbersee, which receives leachate water of high inorganic loading from an upgradient landfill site. The highly concentrated sulfate ion in groundwater, when entering the pore water system of the lake, gives rise to an intensive microbial sulfate reduction. A diagenetic approach was used to explain the existence of a marine-like aqueous system within a geologically slightly acidic aquifer, consisting of a well-buffered lake water and an alkalinity producing, excess sulphide containing sediment pore water system. 相似文献
47.
本文对EDTA滴定过量Pb间接测定SO_4~(2-)的方法作了改进。加入乙醇抑制PbSO_4沉淀的溶解,使滴定不需分离沉淀而直接进行。用六次甲基四胺调节控制pH为5.2—5.4,可避免大量共存Ca~(2+)、Mg~(2+)的干扰。改进后的方法简单、快速,准确度和精密度均好,可适用SO_4~(2-)含量高于1mg/L的天然水分析。 相似文献
48.
William R. Stockwell 《Journal of Atmospheric Chemistry》1994,19(3):317-329
The rates and mechanisms of both gas and liquid phase reactions for the oxidation of sulfur dioxide play an important role in the production of atmospheric acids and aerosol particles. Rhodeet al. (1981) concluded that sulfate production rates were highly non-linear functions of sulfur dioxide emission rates. Their modelling study used an HO
x
termination mechanism for the HO—SO2 reaction in the gas-phase. Stockwell and Calvert (1983) determined that one of the products of the overall reaction of HO with sulfur dioxide was an HO2 radical. The National Research Council (1983) using a version of the Rhodeet al. (1981) model modified to include HO2 production from the HO—SO2 reaction concluded that sulfate production becomes much more linear with respect to reductions in sulfur dioxide emissions. However, the cause of this increased linearity was not explained by the National Research Council report. It is demonstrated that the increased linearity is due to the coupling of gas-phases and aqueous phase chemistry. The gas-phase sulfur dioxide oxidation mechanism has a very significant effect on hydrogen perodide production rates. 相似文献
49.
Jean Servant Robert Delmas Jacques Rancher Marcel Rodriguez 《Journal of Atmospheric Chemistry》1984,1(4):391-401
A partial balance of mineral N is given for the basins of two coastal rivers in a forest zone in the Ivory Coast. The dry and wet depositions on the basin surfaces is given for particulate matter (NO3
–, NH4
+). The quantity of mineral N washed away in the rivers is evaluated. The losses from leaching of the soils by rainwater are about 0.33 to 1.0% of the atmospheric depositions for NH4
+–N and 2.2 to 5.8% for NO3
––N. The yearly atmospheric input of N compounds to the ecosystem, about 1.4 g N m–2 y–1, is at least 14% of mineral N formed in the soils and is therefore quite significant. 相似文献
50.
Trace metals in acid sediments and waters, Pimpama catchment, southeast Queensland, Australia 总被引:2,自引:1,他引:2
The Pimpama River floodplain has developed over the last several thousand years as a result of sea-level fluctuations that
shaped the lower catchment and enabled the formation of sedimentary pyrite. The subsequent production of sulfuric acid due
to the oxidation of this pyrite enhances the breakdown of metal-bearing sediments and can lead to leaching of major and trace
metals into the waters of the region. The seasonal pattern of rainfall and current land-use activities are important aspects
that intensify the natural production of acid and influence the release and distribution of metals. To identify the source
and migration of metals in the Pimpama catchment and to understand the impact of pyrite oxidation on the distribution of metals
in sediments and waters, several components of the drainage system were analyzed: bedrock, sediments from river bed and bank,
and water. The elements analyzed in this study (V, Cr, Co, Ni, Cu, Zn and Pb) are all present in the bedrock material which
explains their occurrence in the unconsolidated sediments of the floodplain. These metals concentrate in the upper section
of the sedimentary sequence and their presence is related to clay minerals such as smectite, organic matter and iron phases.
However, Zn, Mo and Co occur in higher amounts than the local background and within standard shale. This comparison suggests
that the diagenetic processes alone cannot explain the higher concentrations and it is concluded that these metals also have
an anthropogenic source. The formation of sulfuric acid creates conditions for higher mobility of some metals, such as Cr,
Co, Ni, Cu, Zn, but does not affect less mobile ones such as Mo and Pb. Over the longterm, the production of acid influences
the breakdown of mineral phases and enhances the process of weathering. Over the short term, every rain event leaches acid
from sediments and mobilizes metals resulting in a substantial reduction in the quality of river water.
Received: 2 October 1998 · Accepted: 16 February 1999 相似文献