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101.
We report on a year's study of spatial and seasonal patterns of zooplankton abundance in Port Phillip and Westernport Bays, July 1982 to August 1983. These two bays, closely adjacent on the southern coast of Victoria, Australia, differ in several respects: Port Phillip is a nearly landlocked bay with a broad basin, while Westernport is an open tidal embayment with extensive mud and seagrass banks. Both bays have a resident zooplankton fauna distinct from that of Bass Strait. Although these resident communities have many species in common, patterns of abundance and dominance are quite different. We found that the holoplankton of Port Phillip was about half copepods, mostly Paracalanus indicus, with 23% Caldocera and 21% larvaceans. Westernport Bay zooplankton was dominated by Acartia tranteri, with no resident cladoceran fauna. Bass Strait species were more often found in Westernport than in Port Phillip Bay, but the resident community of Port Phillip Bay was more similar to that of Bass Strait than to that of Westernport.Although this study was undertaken in an exceptionally dry year, the available historical data show that the overall patterns found in 1982–1983 are typical for these bays. The differences in community composition probably relate to differences in depth profile, predator abundance, and suspended matter between the bays. 相似文献
102.
G.H.L. Read 《Estuarine, Coastal and Shelf Science》1985,21(3):313-324
A dry (1979–1980) and a wet (1980–1981) season had a marked effect on the freshwater inflow into the Keiskamma estuary. Under low inflow conditions, which results in elevated salinities in the upper reaches, an upstream migration of adult Macrobrachium petersi (Hilgendorf) to freshwater takes place. During periods of increased river inflow adult M. petersi move downstream to the more saline reaches of the estuary. These two migratory responses have been interpreted as (a) a breeding migration under high inflow conditions which ensures that larvae are in close proximity to salinities that favour growth and development, and (b) an adult upstream migration back to freshwater to escape elevated estuarine salinities as a result of the low freshwater inflow. 相似文献
103.
R. F. Griffin 《Journal of Astrophysics and Astronomy》1990,11(4):533-540
Photoelectric radial-velocity measurements show that HD 118670 is a double-lined spectroscopic binary in an orbit which is
not quite circular and whose period is about 48 days. Spectral types of K0 V and K7 V would satisfy the photometry and the
mass ratio; the mass function would then suggest the possibility of eclipses. However, actual spectral classification indicates
a luminosity somewhat above the main sequence 相似文献
104.
Simulation of double cold cores of the 35°N section in the Yellow Sea with a wave-tide-circulation coupled model 总被引:1,自引:0,他引:1
Based on the MASNUM wave-tide-circulation coupled numerical model, the temperature structure along 35°N in the Yellow Sea
was simulated and compared with the observations. One of the notable features of the temperature structure along 35°N section
is the double cold cores phenomena during spring and summer. The double cold cores refer to the two cold water centers located
near 122°E and 125°E from the depth of 30m to bottom. The formation, maintenance and disappearance of the double cold cores
are discussed. At least two reasons make the temperature in the center (near 123°E) of the section higher than that near the
west and east shores in winter. One reason is that the water there is deeper than the west and east sides so its heat content
is higher. The other is invasion of the warm water brought by the Yellow Sea Warm Current (YSWC) during winter. This temperature
pattern of the lower layer (from 30m to bottom) is maintained through spring and summer when the upper layer (0 to 30m) is
heated and strong thermocline is formed. Large zonal span of the 35°N section (about 600 km) makes the cold cores have more
opportunity to survive. The double cold cores phenomena disappears in early autumn when the west cold core vanishes first
with the dropping of the thermocline position.
Supported by the National Basic Research Program of China (No. G1999043809) and the National Science Foundation of China (No.
49736190). 相似文献
105.
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
106.
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
107.
THECONSTRUCTIONANDITSDEVELOPMENTOFTHEOVERSEASTRANSPORTSYSTEMINNORTHEASTCHINAGaoShali(高莎丽)(DepartmentofGeography,NortheastNorm... 相似文献
108.
The sand–loess transition zone in north China is sensitive to climate change, and is an ideal place to investigate past environmental changes. However, past climate change at millennial–centennial timescales in this region has not been well reconstructed because of limited numerical dating. Alternations of sandy loam soils with aeolian sand layers in the Mu Us and Otindag sand fields, which lie along the sand–loess transition zone, indicate multiple intervals of dune activity and stability. This change is probably a response to variations of the East Asian monsoon climate during the late Quaternary. The single aliquot regeneration (SAR) optically stimulated luminescence (OSL) dating protocol, which has been successfully applied to aeolian deposits worldwide, is applied to these two sand fields in this study. The OSL ages provide reliable constraints for reconstruction of past climate changes at suborbital timescale. Sections in both sand fields contain aeolian sand beds recording millennial‐scale episodes of dry climate and widespread dune activation, including episodes at about the same time as Heinrich Event 5 and the Younger Dryas in the North Atlantic region. These results demonstrate the potential of aeolian sediments in semi‐arid north China to record millennial‐scale climatic events, and also suggest that dry–wet climate variation at the desert margin in China may be linked to climatic change elsewhere in the Northern Hemisphere, through atmospheric circulation. This article was published online on 27 November 2008. An error was subsequently identified. This notice is included in the online and print versions to indicate that both have been corrected (16 December 2008). Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
109.
110.