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991.
Stephen M. Elardo David S. Draper Charles K. Shearer Jr. 《Geochimica et cosmochimica acta》2011,75(11):3024-5093
Crystallization of the Lunar Magma Ocean (LMO) has been numerically modeled and its products inferred from sample observations, but it has never been fully tested experimentally. This study is a reexamination of the LMO hypothesis by means of the first experimental simulation of lunar differentiation. Two end-member bulk Moon compositions are considered: one enriched in refractory lithophile elements relative to Earth and one with no such enrichment. A “two-stage” model of magma ocean crystallization based on geophysical constraints is simulated and features early crystal suspension and equilibrium crystallization followed by fractional crystallization of the residual magma ocean. An initially entirely molten Moon is assumed. Part 1 of this study, presented here, focuses on stage 1 of this model and considers the early cumulates formed by equilibrium crystallization, differences in mantle mineralogy resulting from different bulk Moon compositions, and implications for the source regions of the highlands Mg-suite.Refractory element enriched bulk Moon compositions produce a deep mantle that contains garnet and trace Cr-spinel in addition to low-Ca pyroxene and olivine. In contrast, compositions without refractory element enrichment produce a deep dunitic mantle with low-Ca pyroxene but without an aluminous phase. The differences in bulk composition are magnified in the residual melt; the residual LMO from the refractory element enriched composition will likely produce plagioclase and ilmenite earlier and in greater quantities. Both compositions produce Mg-rich early cumulate piles that extend from the core-mantle boundary to ∼355 km depth, if 50% equilibrium crystallization and whole Moon melting are assumed. These early LMO cumulates provide good fits for the source regions for a component of the high-Mg∗, Ni- and Co-poor parental magmas of the Mg-suite cumulates, if certain conditions are called upon. The olivine in early LMO cumulates produced by either bulk Moon composition is far too rich in Cr to be reasonable for the source regions of the Mg-suite, meaning either core formation in the presence of S and/or C must be invoked to deplete the LMO and the crystallizing olivine in Cr, or that current estimates of the bulk lunar Cr content are too high. We infer that melts meeting the criteria of the Mg-suite parents could be produced from early LMO cumulates by solid state KREEP and plagioclase hybridization near the base of the crust and subsequent partial melting. Additionally, we propose a revised model for Mg-suite petrogenesis. 相似文献
992.
Daniel Cossa Lars-Eric Heimbürger Stephen R. Rintoul Edward C.V. Butler Andrew R. Bowie Roslyn J. Watson 《Geochimica et cosmochimica acta》2011,75(14):4037-4052
We present here the first mercury speciation study in the water column of the Southern Ocean, using a high-resolution south-to-north section (27 stations from 65.50°S to 44.00°S) with up to 15 depths (0-4440 m) between Antarctica and Tasmania (Australia) along the 140°E meridian. In addition, in order to explore the role of sea ice in Hg cycling, a study of mercury speciation in the “snow-sea ice-seawater” continuum was conducted at a coastal site, near the Australian Casey station (66.40°S; 101.14°E). In the open ocean waters, total Hg (HgT) concentrations varied from 0.63 to 2.76 pmol L−1 with “transient-type” vertical profiles and a latitudinal distribution suggesting an atmospheric mercury source south of the Southern Polar Front (SPF) and a surface removal north of the Subantartic Front (SAF). Slightly higher mean HgT concentrations (1.35 ± 0.39 pmol L−1) were measured in Antarctic Bottom Water (AABW) compared to Antarctic Intermediate water (AAIW) (1.15 ± 0.22 pmol L−1). Labile Hg (HgR) concentrations varied from 0.01 to 2.28 pmol L−1, with a distribution showing that the HgT enrichment south of the SPF consisted mainly of HgR (67 ± 23%), whereas, in contrast, the percentage was half that in surface waters north of PFZ (33 ± 23%). Methylated mercury species (MeHgT) concentrations ranged from 0.02 to 0.86 pmol L−1. All vertical MeHgT profiles exhibited roughly the same pattern, with low concentrations observed in the surface layer and increasing concentrations with depth up to an intermediate depth maximum. As for HgT, low mean MeHgT concentrations were associated with AAIW, and higher ones with AABW. The maximum of MeHgT concentration at each station was systematically observed within the oxygen minimum zone, with a statistically significant MeHgTvs Apparent Oxygen Utilization (AOU) relationship (p < 0.001). The proportion of HgT as methylated species was lower than 5% in the surface waters, around 50% in deep waters below 1000 m, reaching a maximum of 78% south of the SPF. At Casey coastal station HgT and HgR concentrations found in the “snow-sea ice-seawater” continuum were one order of magnitude higher than those measured in open ocean waters. The distribution of HgT there suggests an atmospheric Hg deposition with snow and a fractionation process during sea ice formation, which excludes Hg from the ice with a parallel Hg enrichment of brine, probably concurring with the Hg enrichment of AABW observed in the open ocean waters. Contrastingly, MeHgT concentrations in the sea ice environment were in the same range as in the open ocean waters, remaining below 0.45 pmol L−1. The MeHgT vertical profile through the continuum suggests different sources, including atmosphere, seawater and methylation in basal ice. Whereas HgT concentrations in the water samples collected between the Antarctic continent and Tasmania are comparable to recent measurements made in the other parts of the World Ocean (e.g., Soerensen et al., 2010), the Hg species distribution suggests distinct features in the Southern Ocean Hg cycle: (i) a net atmospheric Hg deposition on surface water near the ice edge, (ii) the Hg enrichment in brine during sea ice formation, and (iii) a net methylation of Hg south of the SPF. 相似文献
993.
Alexander Heuser Thomas Tütken Stephen J.G. Galer 《Geochimica et cosmochimica acta》2011,75(12):3419-8
We present the first systematic study of Ca isotopes (δ44/40Ca) in Late Triassic to Late Cretaceous dinosaur bones and teeth (enamel and dentin) from sympatric herbivorous and carnivorous dinosaurs. The samples derive from five different localities, and data from embedding sediments are also presented. Additional δ44/40Ca in skeletal tissues from modern reptiles and birds (avian dinosaurs) were measured for comparison in order to examine whether the original Ca isotopic composition in dinosaur skeletal apatite was preserved or might have changed during the diagenesis and fossilization process.δ44/40Ca of fossil skeletal tissues range from −1.62‰ (Tyrannosaurus rex enamel) to +1.08‰ (Brachiosaurus brancai bone), while values in modern archosaur bones and teeth range from −1.63‰ (caiman enamel) to −0.37‰ (ostrich bone). The average δ44/40Ca of the three types of fossil skeletal tissue analyzed - bone, dentin and enamel - show some systematic differences: while δ44/40Ca in bone exhibits the highest values, while δ44/40Ca in enamel has the lowest values, and dentin δ44/40Ca falls in between. Values of δ44/40Ca in the remains of herbivorous dinosaurs (0.1-1.1‰) are generally higher than those of bones of modern mammalian herbivores (−2.6‰ to −0.8‰) and from modern herbivorous archosaurs, which exhibit intermediate δ44/40Ca (−0.8‰ to −0.4‰). These systematic isotopic shifts may reflect physiological differences between dinosaurs, mammals and reptiles representing different taxonomic groups of vertebrates.Systematic offsets in skeletal apatite δ44/40Ca between herbivorous and carnivorous dinosaurs are not obvious, indicating a lack of a clear-cut Trophic Level Effect (TLE) shift between herbivores and carnivores in dinosaurs. This observation can be explained if the carnivorous dinosaurs in this study fed mainly on soft tissues from their prey and did not ingest hard (calcified) tissue to much extent. The most striking indication that the primary δ44/40Ca is actually preserved in most of the fossil teeth is a difference in δ44/40Ca of about 0.35 ± 0.10‰ (1SD) between dentin and enamel, based upon 11 of 16 analyzed dentin-enamel pairs. This difference is close to that found in modern reptiles (0.28 ± 0.05‰), and strongly suggests that this tell-tale signature is a primary feature of the fossilized dinosaur material as well. Furthermore, simple mass balance calculations show that changes of the original δ44/40Ca in bones and teeth by diagenetically-formed calcium-bearing minerals are either small or would require implausible high original δ44/40Ca values in the skeletal apatite. 相似文献
994.
Remediation of U-contaminated sites relies upon thermodynamic speciation calculations to predict U(VI) movement in the subsurface. However, reliability and applicability of geochemical speciation and reactive transport models may be limited by determinate (model) errors and random (uncertainty) errors in the equilibrium speciation calculations. This study examines propagated uncertainty in two types of subsurface calculations: I. Dissolved U(VI) speciation based on measured analytical constraints and solution phase equilibria and II. Overall U(VI) speciation which combined the dissolved phase equilibria with previously published adsorption reactions. Three levels of uncertainty, instrumental uncertainty, temporal variation and spatial variation across a site, were investigated using first-derivative sensitivity calculations and Monte Carlo simulations. Dissolved speciation calculations were robust, with minimal amplification of uncertainty and normal output distributions. The most critical analytical constraints in the dissolved system are pH, DIC, total U and total Ca, with some effect from dissolved . When considering adsorption equilibria, calculations were robust with respect to adsorbed U(VI) concentration prediction, but bimodal distributions of dissolved U(VI) concentrations were observed in simulations with background levels of total U(VI) and higher (spatial and temporal variability) estimates of input uncertainty. Consequently, sorption model predictions of dissolved U(VI) may not be robust with respect these higher levels of uncertainty. 相似文献
995.
Katherine E. Wright Stephen E. Grasby Charles Williamson John Spear Alexis S. Templeton 《Applied Geochemistry》2011
The authors are studying microbial sulfur redox metabolisms in a glacial environment. The energy available from sulfur redox reactions at this site has been calculated using geochemical data obtained from the site. DNA has been extracted from the same site and is being analyzed for the presence and relative quantities of sulfur redox genes, to determine whether bioenergetic calculations can predict the sulfur redox reactions that microbes are in fact utilizing. 相似文献
996.
The interactions of organic matter and minerals contribute to the capacity of soils to store C. Such interactions may be controlled by the processes that determine the availability of organic matter and minerals, and their physical contacts. One of these processes is bioturbation, and earthworms are the best known organisms that physically mix soils. Earthworms are not native species to areas previously glaciated, and the introduction of earthworms to these regions has been associated with often dramatic changes in soil structure and geochemical cycles. The authors are studying C mineral interaction along an approximately 200 m long earthworm invasion transect in a hardwood forest in northern Minnesota. This transect extends from the soils where earthworms are absent to soils that have been invaded by earthworms for nearly 30–40 years. Pre-invaded soils have an approximately 5 cm thick litter layer, thin (~5 cm) A horizon, silt rich E horizon, and clay-rich Bt horizons. The A and E horizons formed from aeolian deposits, while the clay-rich Bt horizons probably developed from underlying glacial till. With the advent of earthworm invasion, the litter layer disappears and the A horizons thicken at the expense of the O and E horizons. In addition, organic C contents in the A horizons significantly increase with the arrival of earthworms. Simultaneously, measured mineral specific surface areas suggest that minerals’ capacities to complex the organic matter appear to be greater in soils with active earthworm populations. Based on the data from two end member soils along the transect, mineral specific surface areas in the A and E horizons are larger in the earthworm invaded soil than in the pre-invasion soil. Additionally, within < 5 a of earthworm invasions, A horizon materials are turned from single grain to a strong medium granular structure. While A horizon organic matter content and organic C-mineral complexation increase after earthworm invasion, they are also more vigorously mixed. This growing data set, when ultimately combined with ongoing measurements of (1) the population dynamics of earthworms along the invasion transect, (2) C-mineral association (via surface adsorption and physical collusion in mineral aggregates) and (3) dissolved organic C will show how and how much soil capacity to store C is affected by burrowing organisms, which are often the keystone species of given ecosystems. 相似文献
997.
Chunfa Wu Jiaping Wu Yongming Luo Haibo Zhang Ying Teng Stephen D. DeGloria 《Environmental Earth Sciences》2011,63(5):1093-1103
It was not unusual in soil and environmental studies that the distribution of data is severely skewed with several high peak
values, which causes the difficulty for Kriging with data transformation to make a satisfied prediction. This paper tested
an approach that integrates kriging and triangular irregular network interpolation to make predictions. A data set consisting
of total Copper (Cu) concentrations of 147 soil samples, with a skewness of 4.64 and several high peak values, from a copper
smelting contaminated site in Zhejiang Province, China. The original data were partitioned into two parts. One represented
the holistic spatial variability, followed by lognormal distribution, and then was interpolated by lognormal ordinary kriging.
The other assumed to show the local variability of the area that near to high peak values, and triangular irregular network
interpolation was applied. These two predictions were integrated into one map. This map was assessed by comparing with rank-order
ordinary kriging and normal score ordinary kriging using another data set consisting of 54 soil samples of Cu in the same
region. According to the mean error and root mean square error, the approach integrating lognormal ordinary kriging and triangular
irregular network interpolation could make improved predictions over rank-order ordinary kriging and normal score ordinary
kriging for the severely skewed data with several high peak values. 相似文献
998.
999.
The status of water quality of Irish estuaries is reviewed; this sheds light on the rationale behind the design of the national monitoring programme. Relative to other EU Member States, Ireland's coastal monitoring programme is relatively young and not as advanced. The monitoring programmes in Ireland pre Water Framework Directive (WFD) were structured on a salinity-based typology, with an emphasis on quantifying the variability of the component elements. Although monitoring is a significant obligation under the WFD, there is little guidance on developing monitoring protocols; Member States are developing ad hoc monitoring programme. The Irish Environmental Protection Agency (EPA), responsible authority, undertook research programmes to assist design and implementation of the WFD. A substantial new national monitoring programme was developed. However, the Irish programme is not optimised; the programme is being refined to include elements not yet covered, notably the biota. New research, by the authors, aims to develop a robust approach towards monitoring integrating data and model results. This paper presents changes in Irish marine water quality monitoring policy and some of the associated research necessary to change policy. 相似文献
1000.
Hamish A. Malcolm Peter L. DaviesAlan Jordan Stephen D.A. Smith 《Deep Sea Research Part II: Topical Studies in Oceanography》2011,58(5):616-627
Improved understanding of the East Australian Current (EAC) and sea-temperature patterns within the Solitary Islands region of northern New South Wales, an area where tropical and temperate faunas overlap, is an essential step in explaining cross-shelf gradients in biotic patterns. Sea temperature at ∼10 m was logged using thermistors at seven stations every 30 minutes between January 2001 and December 2008. Stations were replicated in three distance-from-shore categories (<1.5; 1.5 to 6; and >6 km from the coast), corresponding with predominant assemblage patterns of reef fish. Daily, monthly, seasonal and yearly sea-temperature patterns were compared between and within stations and distance-from-shore categories. SST images were examined to determine the role of the EAC in producing short-period (2 to 4 days) temperature anomalies. Sea temperatures ranged between 16.6-27.5 °C and were highest offshore and lowest inshore. Offshore sites experienced average temperatures ∼1 °C higher than nearshore sites over the 8-year study. There was considerable variation in sea temperature between years, with 2002 and 2006 being the warmest and 2007 the coolest. These patterns correspond with strong inter-annual variability of the EAC at the scale of the Solitary Islands region. The EAC influenced shelf waters most strongly during late spring/summer when temperatures were also most variable over the smallest temporal scales (hours, days). Short-period anomalies between and within stations could largely be explained by variable encroachment of the EAC across the shelf and/or colder intrusions of water forming adjacent to the coastline. Previous assumptions that the EAC strongly influences gradients in the distribution of tropical species in this nearshore region are strongly supported. 相似文献