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91.
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   
92.
93.
During aircraft flights in May 1981 from Munich (40°N) to north of the Spitsbergen Islands (82°N) and to Monrovia, Liberia (6°N), air samples were obtained in the altitude range of 8 to 11 km and during the ascents and descents near the airports. These samples have been analyzed for the trace gas mixing ratios of CH4, CO and N2O. The results of these analyses are presented and discussed.The results provide new evidence of tropospheric-stratospheric exchange events in the vicinity of the subpolar and subtropical tropopause foldings and possibly show a case of transport of CO-enriched air in the upper troposphere above the North Atlantic Ocean.  相似文献   
94.
New CH4 emission data from a number of Northern and Southern Hemispheric, tropical and temperate termites, are reported, which indicate that the annual global CH4 source due to termites is probably less than 15 Tg. The major uncertainties in this estimate are identified and found to be substantial. Nevertheless, our results suggest that termites probably account for less than 5% of global CH4 emissions.  相似文献   
95.
Formation of methoxy (CH3O) radicals in the reaction (1) CH3O2+NOCH3O+NO2 at 298 K has been observed directly using time resolved LIF. The branching ratio % MathType!MTEF!2!1!+-% feaafeart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaeqOXdyMaae% 4qaiaabIeadaWgaaWcbaGaae4maaqabaGccaqGpbGaaeiiaiaabIca% ieqacaWF9aGaa8hiaiaa-nbicaWFGaGaeuiLdqKaai4waiaaboeaca% qGibWaaSbaaSqaaiaabodaaeqaaOGaae4taiaac2facaWFVaGaeuiL% dqKaai4waiaaboeacaqGibWaaSbaaSqaaiaabodaaeqaaOGaae4tam% aaBaaaleaacaqGYaaabeaakiaac2facaqGPaaaaa!4E31!\[\phi {\rm{CH}}_{\rm{3}} {\rm{O (}} = -- \Delta [{\rm{CH}}_{\rm{3}} {\rm{O}}]/\Delta [{\rm{CH}}_{\rm{3}} {\rm{O}}_{\rm{2}} ]{\rm{)}}\] has been determined by quantitative cw-UV-laser absorption at 257 nm of CH3O2 and CH3ONO, the product of the consecutive methoxy trapping reaction (2) % MathType!MTEF!2!1!+-% feaafeart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaae4qaiaabI% eadaWgaaWcbaGaae4maaqabaGccaqGpbacbeGaa83kaiaa-bcaieaa% caGFobGaa43taiaa+bcacaGFOaGaa83kaiaa+1eacaGFPaGaa4hiai% abgkziUkaabccacaqGdbGaaeisamaaBaaaleaacaqGZaaabeaakiaa% b+eacaqGGaGaaeOtaiaab+eacaqGGaGaa4hkaiaa-TcacaGFnbGaa4% xkaiaa+5cacaGFGaGaa4hiaiabeA8aMnaaBaaajqwaacqaaiaaboea% caqGibWaaSbaaKazcaiabaGaae4maaqabaqcKfaGaiaab+eaaSqaba% aaaa!55AC!\[{\rm{CH}}_{\rm{3}} {\rm{O}} + NO ( + M) \to {\rm{ CH}}_{\rm{3}} {\rm{O NO }}( + M). \phi _{{\rm{CH}}_{\rm{3}} {\rm{O}}} \] is found to be (1.0±0.2). The rate constant k 1 is (7±2) 10-12 cm3/molecule · s in good agreement with previous results.  相似文献   
96.
A series of 149 measurements of the HCHO mixing ratio were made between 0 and 10 km altitude and 70° N to 60° S latitude during TROPOZ II. The data show a vertical decrease of the HCHO mixing ratio with altitude at all latitudes and a broad latitudinal maximum in the HCHO mixing ratio between 30° N and 30° S at all altitudes. The measured mixing ratios of HCHO are considerably higher than those expected from CH4 oxidation alone, but agree broadly with the average latitude by altitude distribution of HCHO derived by a 2D model including emissions of C1–C7 hydrocarbons. A number of the regional scale deviations of the measured HCHO distribution from the average modelled one can be explained in terms of the local wind field.  相似文献   
97.
From July to September of 1990,CH_4 flux measurements were made in Lin'an rice paddies using gradient profiletechniques.Some characteristics of the turbulence structure under the stable conditions have been verified in the surfacelayer according to the in situ measurements.The semi-empirical turbulent parameters β_m,β_h and β_c and their changeswith the stability parameter Ri are given.Observed results indicate that CH_4 flux in the rice-paddy is mainly decided bythe methnogenesis and the process of CH4 transport from internal soils to the atmosphere,and that the CH_4 verticaltransfer is depressed in the stable surface layer.The CH_4 flux shows that its obvious diurnal changes,and the meanCH_4 flux are higher in nighttime and lower in daytime,and the peaks appear at about 2000 BST at night and 0300 BSTin the early morning,respectively.The mean value of CH_4 flux is about 4.18±2.3 mg/m~2 h.  相似文献   
98.
From July to September of 1990,CH4 flux measurements were made in Lin'an rice paddies using gradient profile techniques.Some characteristics of the turbulence structure under the stable conditions have been verified in the surface layer according to the in situ measurements.The semi-empirical turbulent parameters βmh and βc and their changes with the stability parameter Ri are given.Observed results indicate that CH4 flux in the rice-paddy is mainly decided by the methnogenesis and the process of CH4 transport from internal soils to the atmosphere,and that the CH4 vertical transfer is depressed in the stable surface layer.The CH4 flux shows that its obvious diurnal changes,and the mean CH4 flux are higher in nighttime and lower in daytime,and the peaks appear at about 2000 BST at night and 0300 BST in the early morning,respectively.The mean value of CH4 flux is about 4.18±2.3 mg/m2 h.  相似文献   
99.
唐茂  赵辉  刘耘 《矿物学报》2007,27(3):396-399
不同成因的天然气由于形成温度不同,往往会有不同的稳定同位素特征。但是,由于经常不能同时获得天然气以及它的生成母体的同位素成分,很难用单独的C或H同位素成分来确定它的形成温度。在形成天然气时,不同的温度会形成不同的二元同位素的浓度,温度越低,二元同位素的比例越大,因此只需要知道天然气本身的二元同位素的浓度,就可以确定形成温度,从而避免了需要知道天然气生成母体的同位素成分这一难题。本文利用高级量子化学计算,预测了不同温度下天然气中甲烷和CO2气体的二元同位索(Clumped isotope)的特征,提供用于天然气成因分析的新方法。  相似文献   
100.
Expounded in this work are the results of critical consideration of published and original data on biologic nature and appearance chronology of different groups of Archean and Lower Proterozoic (3.5–1.65 Ga) paleontological remains known from geological record. Conclusions are substantiated by morphological analysis of structurally preserved microfossils, their facies distribution, and by inferable genesis and principal evolutionary trends of Archean stromatolites. A special attention is paid to variations of organic and carbonate carbon isotope composition in sedimentary successions with paleontological remains and to recent information about discovered, most ancient biomarkers of large groups of organic world. As a result of this approach, a detailed model of Precambrian organic world evolution is suggested.  相似文献   
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