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1.
1 IntroductionBacteriaandtheiractivitiesplayanimportantroleintheelementalbiogeochemicalcyclesandenergytransformingintheocean (Zhenetal.1 997) .DortchandPackard(1 989) proposedthatfoodwebsintheeutrophicwatersaredominatedbythebiomassofprimaryproducerswhilefoodwebsintheoligotrophicwatersaredominatedbythebiomassofmicrobes.Heterotrophicbacteriahadbeenshowntoplayanimportantroleinthedecompositionoflarge ,rapidlysinkingorganicparticleswithinandbelowtheeuphot iczone ,andfurthertoaffecttheelementaldyn… 相似文献
2.
In the upper Chesapeake Bay (Maryland, U.S.A.) field surveys were conducted at 18 multiple longshore sand bar sites. The multiple bar systems were found in water depths less than approximately 2 m (mean sea level), and exhibited mild bottom slopes of 0·0052 or less. The number of bars composing each system ranged from four to 17 and the spacing between the crests typically increased in the offshore direction, ranging from 12 to 70 m. Bar height also typically increased with distance offshore and ranged from 0·03 to 0·61 m. A grain size analysis of crest and trough sediment did not reveal any significant differences and the sediment was categorized as ‘fine sand’. A review of the literature data indicated that the Chesapeake Bay multiple bars possessed similar characteristics to those found in Gelding Bay (Baltic Sea); similarities in fetch, wave height and tidal range between the two bays may account for this finding. The surf-scaling parameter indicated that the multiple bar systems were extremely dissipative with regard to wave energy, and wave height appeared to be an important factor in controlling bar spacing and bar height. A multiple wave break point hypothesis was discussed as a possible mechanism for the formation of Chesapeake Bay multiple longshore bars, and limited observational evidence appeared to support such a mechanism. 相似文献
3.
Ren Tinawi Marc Sarrazin Andr Filiatrault 《Soil Dynamics and Earthquake Engineering》1993,12(8):469-477
The 1990 edition of the National Building Code of Canada (Associate Committee of the National Building Code, National Research Council, Ottawa, 1990) makes a clear distinction between eastern and western Canada in terms of seismic acceleration and velocity zones. While it is well established that ground motions can be amplified significantly through loose clay deposits, no results are available that take into consideration the typical high frequency content of ground motions in eastern Canada. This paper develops ground amplification curves for clays having depths between 10 and 70 m excited by typical eastern Canadian ground motions scaled to two different values of peak horizontal accelerations. Simplified free-field spectral design curves, which could be used by structural designers, are proposed. The curves show that maximum spectral accelerations occur for structural periods between 0.2 and 0.5 s. In addition, soil depth does not appear to be an important parameter controlling the response of typical clay deposits in eastern Canada. 相似文献
4.
Donald C. Gordon Peter J. Cranford Con Desplanque 《Estuarine, Coastal and Shelf Science》1985,20(2):205-227
The Cumberland Basin, a 118 km2 estuary at the head of the Bay of Fundy which has an average tidal range of about 11m, contains large tracts of salt marsh (15% of the area below highest high water). Low marsh (below about 0·9 m above mean high water) is composed almost exclusively of Spartina alterniflora while the vegetation on high marsh is more diverse but dominated by Spartina patens. Because of its higher elevation, high marsh is flooded infrequently for short periods by only extreme high tides. Low marsh is inundated much more frequently by water as much as 4m deep for periods as long as 4 h per tide. Temporal variability in the occurrence of extreme tides influences the flooding frequency of high marsh for any given month and year. Using a modification of Smalley's method, the mean annual net aerial primary production (NAPP) of low and high marsh is estimated to be 272 and 172 g C m?2, respectively. Vegetation turnover times average 1·0 and 2·0 y for low and high marsh, respectively. Because of abundant tidal energy, much of the low marsh production appears to be exported and distributed widely about the estuary. Since high levels of turbidity suppress phytoplankton production, salt marshes produce approximately half of the carbon fixed photosynthetically in the Cumberland Basin. It is concluded that salt marshes play a major ecological role in the Cumberland Basin. 相似文献
5.
6.
Replicate portions of a Delaware salt marsh were enclosed in cylindrical microcosms and exposed to elevated levels of inorganic arsenic (arsenate). All biotic and abiotic components in dosed cylinders rapidly incorporated arsenic. Spartina blades showed the greatest arsenic enrichment, with dosed plants incorporating arsenic concentrations an order of magnitude higher than controls. Spartina detritus and sediments also exhibited greatly elevated arsenic concentrations. Virtually all of the arsenic was incorporated into plant tissue or strongly sorbed to cell surfaces. Thus, elevated arsenic concentrations in estuarine waters will be reflected in living and non-living components of a salt marsh ecosystem, implying that increased arsenic will be available to organisms within the marsh ecosystem. 相似文献
7.
Silicon limitation on primary production and its destiny in Jiaozhou Bay, China——Ⅳ:Study on cross-bay transect from estuary to ocean 总被引:1,自引:0,他引:1
The authors analyzed the data collected in the Ecological Station Jiaozhou Bay from May 1991 to November 1994, including 12
seasonal investigations, to determine the characteristics, dynamic cycles and variation trends of the silicate in the bay.
The results indicated that the rivers around Jiaozhou Bay provided abundant supply of silicate to the bay. The silicate concentration
there depended on river flow variation. The horizontal variation of silicate concentration on the transect showed that the
silicate concentration decreased with distance from shorelines. The vertical variation of it showed that silicate sank and
deposited on the sea bottom by phytoplankton uptake and death, and zooplankton excretion. In this way, silicon would endlessly
be transferred from terrestrial sources to the sea bottom. The silicon took up by phytoplankton and by other biogeochemical
processes led to insufficient silicon supply for phytoplankton growth. In this paper, a 2D dynamic model of river flow versus
silicate concentration was established by which silicate concentrations of 0.028–0.062 μmol/L in seawater was yielded by inputting
certain seasonal unit river flows (m3/s), or in other words, the silicate supply rate; and when the unit river flow was set to zero, meaning no river input, the
silicate concentrations were between 0.05–0.69 μmol/L in the bay. In terms of the silicate supply rate, Jiaozhou Bay was divided
into three parts. The division shows a given river flow could generate several different silicon levels in corresponding regions,
so as to the silicon-limitation levels to the phytoplankton in these regions. Another dynamic model of river flow versus primary
production was set up by which the phytoplankton primary production of 5.21–15.55 (mgC/m2·d)/(m3/s) were obtained in our case at unit river flow values via silicate concentration or primary production conversion rate.
Similarly, the values of primary production of 121.98–195.33 (mgC/m2·d) were achieved at zero unit river flow condition. A primary production conversion rate reflects the sensitivity to silicon
depletion so as to different phytoplankton primary production and silicon requirements by different phytoplankton assemblages
in different marine areas. In addition, the authors differentiated two equations (Eqs. 1 and 2) in the models to obtain the
river flow variation that determines the silicate concentration variation, and in turn, the variation of primary production.
These results proved further that nutrient silicon is a limiting factor for phytoplankton growth.
This study was funded by NSFC (No. 40036010), and the Director's Fund of the Beihai Sea Monitoring Center, the State Oceanic
Administration. 相似文献
8.
Autotrophic biomass and productivity as well as nutrient distributions and phytoplankton cell populations in the James River estuary, Virginia, were quantified both spatially and temporally over a 17-month period. Emphasis was placed on the very low salinity region of the estuary in order to gain information on the fate of freshwater phytoplankters. Differing amounts of freshwater plant biomass are advected into the estuary as living material, DOC or POC and the demonstrated variability of this input must play an important role in marine biogeochemical cycling.Late summer and fall maxima in both chlorophyll a and the photosynthetic production of particulate organic carbon in very low salinity regions were inversely correlated with river discharge.During periods of low river discharge greater than 50% of the chlorophyll a biomass measured at 0‰ disappeared within a narrow range of salinity (0–2‰). Cell enumeration data suggest that species introduced from the freshwater end-member tend to comprise the bulk of the biomass removed. Confounding factors, which may contribute to the regulation of both the abundance and species of phytoplankters mid-river, include the flocculation of colloidal material with phytoplankton cells, the presence of the turbidity maximum and the growth of endemic phytoplankton populations.An inverse relationship exists between the phytoplankton abundance in very low salinity waters and the abundance of biomass measured in the lower portion of the river (estuary). Thus, autotrophic production in the fresh and very low salinity areas may indirectly regulate the onset on the spring bloom in the estuary by controlling the amount of nutrients available. 相似文献
9.
Abstract Eclogites are distributed for more than 500 km along a major tectonic boundary between the Sino-Korean and Yangtze cratons in central and eastern China. These eclogites usually have high-P assemblages including omphacite + kyanite and/or coesite (or its pseudomorph), and form a high-P eclogite terrane. They occur as isolated lenses or blocks 10 cm to 300 m long in gneisses (Type I), serpentinized garnet peridotites (Type II) and marbles (Type III). Type I eclogites were formed by prograde metamorphism, and their primary metamorphic mineral assemblage consists mainly of garnet [pyrope (Prp) = 15–40 mol%], omphacite [jadeite (Jd) = 34–64 mol%], pargasitic amphibole, kyanite, phengitic muscovite, zoisite, an SiO2 phase, apatite, rutile and zircon. Type II eclogites characteristically contain no SiO2 phase, and are divided into prograde eclogites and mantle-derived eclogites. The prograde eclogites of Type II are petrographically similar to Type I eclogites. The mantle-derived eclogites have high MgO/(FeO + Fe2O3) and Cr2O3 compositions in bulk rock and minerals, and consist mainly of pyrope-rich garnet (Prp = 48–60 mol%), sodic augite (Jd = 10–27 mol%) and rutile. Type III eclogites have an unusual mineral assemblage of grossular-rich (Grs = 57 mol%) garnet + omphacite (Jd = 30–34 mol%) + pargasite + rutile. Pargasitic and taramitic amphiboles, calcic plagioclase (An68), epidote, zoisite, K-feldspar and paragonite occur as inclusions in garnet and omphacite in the prograde eclogites. This suggests that the prograde eclogites were formed by recrystallization of epidote amphibolite and/or amphibolite facies rocks with near-isothermal compression reflecting crustal thickening during continent–continent collision of late Proterozoic age. Equilibrium conditions of the prograde eclogites range from P > 26 kbar and T= 500–750°C in the western part to P > 28 kbar and T= 810–880°C in the eastern part of the high-P eclogite terrane. The prograde eclogites in the eastern part are considered to have been derived from a deeper position than those in the western part. Subsequent reactions, manifested by (1) narrow rims of sodic plagioclase or paragonite on kyanite and (2) symplectites between omphacite and quartz are interpreted as an effect of near-isothermal decompression during the retrograde stage. The conditions at which symplectites re-equilibrated tend to increase from west (P < 10 kbar and T < 580°C) to east (P > 9 kbar and T > 680°C). Equilibrium temperatures of Type II mantle-derived eclogites and Type III eclogite are 730–750°C and 680°C, respectively. 相似文献
10.
A growing body of evidence implies that the concept of 'treeless tundra' in eastern and northern Europe fails to explain the rapidity of Lateglacial and postglacial tree population dynamics of the region, yet the knowledge of the geographic locations and shifting of tree populations is fragmentary. Pollen, stomata and plant macrofossil stratigraphies from Lake Kurjanovas in the poorly studied eastern Baltic region provide improved knowledge of ranges of north‐eastern European trees during the Lateglacial and subsequent plant population responses to the abrupt climatic changes of the Lateglacial/Holocene transition. The results prove the Lateglacial presence of tree populations (Betula, Pinus and Picea) in the eastern Baltic region. Particularly relevant is the stomatal and plant macrofossil evidence showing the local presence of reproductive Picea populations during the Younger Dryas stadial at 12 900–11 700 cal. a BP, occurring along with Dryas octopetala and arctic herbs, indicating semi‐open vegetation. The spread of Pinus–Betula forest at ca. 14 400 cal. a BP, the rise of Picea at ca. 12 800 cal. a BP and the re‐establishment of Pinus–Betula forest at ca. 11 700 cal. a BP within a span of centuries further suggest strikingly rapid, climate‐driven ecosystem changes rather than gradual plant succession on a newly deglaciated land. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献