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81.
Abstract

The detailed characteristics of a CASPII warm frontal passage are presented in this article. This storm, Intensive Operating Period (IOP) 13 (February 26–27, 1992), was observed in detail with an array of diverse instruments. It has the advantage over earlier freezing precipitation studies of having simultaneous, in situ and remote sensing measurements by aircraft and ground‐based Doppler radar.

The associated precipitation was in the form of banded structures parallel to the front. Within these bands were embedded precipitation cores, some parallel to the band, some perpendicular. The warm front itself was characterized by major perturbations in its kinematic and thermodynamic features. The cores oriented parallel to the front were the result of embedded convection generated, at least in part, by the irregularities in the frontal surface.

The cores oriented perpendicular to the front were closely associated with the 0°C isotherm on the underside of the frontal inversion. Precipitation phase changes played a significant role in the occurrence of wide near 0°C regions, both vertically and horizontally. These regions had a profound influence on the observed precipitation types and led to complex precipitation‐thermodynamic‐dynamic interactions. Instabilities produced by these interactions are seen in wave‐like features observed by the Doppler radar in these regions, both parallel and perpendicular to the frontal zone.  相似文献   
82.
Seismogenic structures underlie many regions of the vast Canterbury Plains on the South Island of New Zealand. Most of these structures are hidden beneath a layer of rapidly deposited Late Pleistocene sediments, the youth and thickness of which make the general application of conventional paleoseismological studies impractical. In an attempt to improve our understanding of potentially active structures in this region, we have acquired, processed and interpreted shallow seismic reflection data across the northwest Canterbury Plains. To separate the useful reflected signals from unusually high amplitude ambient and source-generated noise, we subjected the data to a specially tailored processing scheme that included time- and space-variant spectral balancing, custom static corrections and mutes, F-X deconvolution, DMO corrections and finite-difference migration. The final stacked and migrated seismic sections supply high-resolution images of the basement and overlying layered Cretaceous- to Quaternary-age supracrustal rocks that have been complexly faulted and folded. At one location, the uppermost Late Pleistocene layers appear to have been gently buckled.  相似文献   
83.
Summary Amphibole data in the MinIdent database (Smith andLeibovitz, 1986) were initially entered using species names quoted in the original source. The database has been updated by reclassifying these early data using the program AMPHTAB supplied by N. M. S. Rock and by adding supplemental data from the more recent literature, with the species names again checked using AMPHTAB. Associated MinIdent mineral identification software was utilized to determine which minerals in the database most closely resemble a series of unknown specimens chemically, as expressed in the Chemical Matching Index, CM, a relative figure-of-merit. Chemical data fromMogessie and Tessadri (1982) and Hawthorne (1983) were used to check the agreement between MinIdent and AMPHTAB for the classification of 221 unknown amphiboles.With 450 amphibole analyses entered and compiled in MinIdent, the name assigned by AMPHTAB showed the highest value of CM in MinIdent for 127 of the 221 unknown amphiboles (57.5°/x) and the second highest value for another 32 (14.5%). A chemically adjacent amphibole field had the highest value of CM for 59 of the 221 unknowns (26.7%), where chemically adjacent refers to a change in one chemical parameter. The greatest discrepancy between the two programs occurred in the hornblendes, with an agreement of just 20%, although for 58% of the unknowns the species with the highest CM in MinIdent was in a chemical field adjacent to the species name assigned by AMPHTAB. In many cases the disagreement between MinIdent and AMPHTAB could be ascribed to a lack of data in MinIdent.A comparison of the two programs suggests that the assignment of a single name to an unknown amphibole by AMPHTAB with no direct indication of its reliability may be; misleading. Standard analytical errors are frequently sufficient to overlap the arbitrary boundaries between amphibole species fields. In such cases it may be preferable to use a program such as MinIdent which, rather than assigning an arbitrary amphibole name, presents a list of 20 amphiboles with the degree of similarity between them and the unknown amphibole indicated. MinIdent offers the additional benefit of allowing input of other than chemical data and bases the match between unknown and standard data upon all input data. This will become more of an advantage as instruments such as automated refractometers become available for routine use.
Zusammenfassung Ausgangspunkt war das Amphibol-Datenmaterial (Smith und Leibovitz, 1986) mit den dort verwendeten Artnamen. Diese Basisdaten wurden vervollständigt und erneuert durch Reklassifizierung mittels des AMPHTAB Programms, ergänzt durch N. M. S. Rock, und durch Hinzufügung weiterer Daten aus der neuesten Literatur, deren Speciesnamen wiederum mit AMPHTAB überprüft wurden. Außerdem wurde eine MinIdent Mineralidentifizierungs-Software verwendet, um die Minerale zu bestimmen, die in ihrem Chemismus am ehesten einer Serie von unbekannten Amphibol-Species entsprechen, wie sie im Chemical Matching Index (CM) aufscheinen. Zur Klassifikation von 221 unbekannten Amphibolen wurden chemische Daten von Mogessie und Tessadri (1982) verwendet um die Übereinstimmung zwischen MinIdent und AMPHTAB zu überprüfen.Unter den 450 in MinIdent zusammengestellten und eingegebenen Amphibolanalysen zeigen die bei AMPHTAB angegebenen die höchsten CM Werte, nämlich 127 von 221 unbekannten Amphibolen (57,5%) und weitere 32 (14,5%) die zweithöchsten Werte. Innerhalb eines chemisch benachbarten Amphibolfeldes hatten 59 der 221 unbekannten Amphibole (26,7%) die höchsten CM Werte, wobei unter achemisch benachbart die Änderung eines chemischen Parameters zu verstehen ist. Die größten Unterschiede zwischen den beiden Programmen traten bei den Hornblenden auf. Die Übereinstimmung lag bei nur 20%, obwohl bei 58% der unbekannten Amphibole die Species mit dem höchsten CM Wert in MinIdent in ein chemisches Feld zu liegen kamen, welches zu den bei AMPHTAB angegebenen Speciesnamen eine benachbarte Position einnimmt. Die Unterschiede zwischen MinIdent und AMPHTAB könnten in vielen Fällen auf ein Fehlen von Daten in MinIdent zurükzuführen sein.Ein Vergleich beider Programme deutet an, daß die Angabe eines Einzelnamens für ein unbekanntes Amphibol im AMPHTAB Programm ohne Angaben über die Zuverlässigkeit zu Mißverständnissen führen kann. Normale analytische Fehler können bereits dazu führen, daß die Grenzen zweier willkürlicher Amphibolfelder überlappen. In derartigen Fällen emphiehlt sich die Anwendung des MinIdent Programmes, welches eben nicht einen willkürlichen Amphibolnamen angibt, sondern eine Liste von 20 Amphibolen mit dem Grad ihrer Ähnlichkeit, und einem Hinweis auf den unbekannten Amphibol. MinIdent bietet den zusätzlichen Vorteil, daß man außer chemischen auch andere Daten eingeben kann, und stellt dann sämtliche Daten des unbekannten Amphibols den Standard Daten gegenüber. Dieser Klassifizierungsvorgang wird mit der zunehmenden Routineanwendung von automatischen Refraktometern verstärkte Anwendung finden.
  相似文献   
84.
An inexpensive, lightweight stream sampler is described which provides a method for continuous collection of suspended stream sediments. The IS3* sampler collects integrated suspended stream samples, and because the sampler relies on basic sedimentation principles, it can be deployed to collect suspended sediment stream samples for environmental studies or geochemical exploration in remote areas. The sampler trapped from 0.45 to 1.2 g of dry sediment during 7- to 8-d field tests conducted during 1985.  相似文献   
85.
The areal outflow of ice through Fram Strait during the period 1953–1984 is estimated on a monthly basis from the geostrophic wind and the ice concentration. Summer ice coverage in various sectors of the Arctic is then compared with the computed outflow through Fram Strait in various antecedent periods. Lag correlations indicate that interannual variations of summer ice severity in the Pacific side of the Arctic Basin are consistent with fluctuations of Fram Strait outflow during the previous 3–9 months. The findlings suggest that above-normal outflow of multiyear ice during the winter/spring months may precondition the large-scale pack ice to respond more directly to offshore flow events during the ensuing months.The areas of highest correlation with Fram Strait outflow undergo a pronounced shift in the early 1970's. Coincident changes in the large-scale circulation pattern imply that the source region of the Transpolar Drift Stream shifted westward from the Alaskan to the Siberian waters during this period.  相似文献   
86.
We have obtained infrared and Raman spectra for garnets synthesized at high (static) pressures and temperatures along the join Mg3Al2Si3O12 (pyrope) — Mg4Si4O12 (magnesium majorite). The vibrational spectra of Mg-majorite show a large number of additional weak peaks compared with the spectra of cubic pyrope garnet, consistent with tetragonal symmetry for the MgSiO3 garnet phase. The Raman bands for this phase show no evidence for line broadening, suggesting that Mg and Si are ordered on octahedral sites in the garnet. The bands for the intermediate garnet compositions are significantly broadened compared with the end-members pyrope and Mg-majorite, indicating cation disorder in the intermediate phases. Solid state 27Al NMR spectroscopy for pyrope and two intermediate compositions show that Al is present only on octahedral sites, so the cation disorder is most likely confined to Mg-Al-Si mixing on the octahedral sites. We have also obtained a Raman spectrum for a natural, shock-produced (Fe,Mg) majorite garnet. The sharp Raman peaks suggest little or no cation disorder in this sample.  相似文献   
87.
An examination of typical tropospheric ozone variability on daily, monthly, annual and interannual timescales and instrumental precision indicates that the current ozonesonde network is insufficient to detect a trend in tropospheric ozone of 1% per year at the 2 level even at stations with records a decade in length. From a trend prediction analysis we conclude that in order to detect a 1% per year trend in a decade or less it will be necessary to decrease the time between observations from its present value of 3–7 days to 1 day or less. The spatial distribution of the current ozonesonde stations is also inadequate for determining the global climatology of ozone. We present a quantitative theory taking into account photochemistry, surface deposition, and wind climatology to define the effectively sampled region for an observing station which, used in conjunction with the instrumental precision and the above prediction analysis, forms the basis for defining a suitable global network for determining regional and global ozone climatology and trends. At least a doubling of the present number of stations is necessary, and the oceans, most of Asia, Africa, and South America are areas where more stations are most needed. Differential absorption lidar ozone instruments have the potential for far more frequent measurements of ozone vertical profiles and hence potentially more accurate climatology and trend determinations than feasible with ozonesondes but may produce a (fair weather) biased data set above the cloud base. A strategy for cloudy regions in which either each station utilizes both lidars and sondes or each station is in fact a doublet comprised of a near-sea-level lidar and a proximal-mountain-top lidar could serve to minimize this bias.  相似文献   
88.
Four state-of-the-art ground water sampling systems were analyzed to determine their reliability in providing representative samples of the volatile chlorinated hydrocarbons trichloroethylene (TCE), perchloroethylene (PCE), and 1,1,1-trichloroethane (TCA) from a simulated monitoring well. The sampling systems studied represent four commonly used devices, including a stainless steel and Teflon® piston pump, a Teflon bailer, a Teflon bladder pump, and a PVC air-lift pump.
Controlled laboratory sampling experiments were conducted in a tank and well test chamber designed to approximate field conditions. A well purging and sampling procedure was used in the test apparatus to determine the accuracy and precision of each device for detecting low concentrations of the compounds in ground water. The compounds selected are some of the most ubiquitous hazardous contaminants found in shallow aquifers near hazardous waste sites throughout the United States.
No significant statistical difference was found among the four sampling systems in detecting the compounds.  相似文献   
89.
Wadsleyite (β-(Mg,Fe)2SiO4) is a major constituent of the Earth's transition zone and is known to accommodate OH. The portion of the transition zone between 400–550 km could be an important source or sink for hydroxyl in plumes and slabs intersecting this region. Micro-infrared spectroscopy has been carried out on the β-phase and coexisting metastable olivine synthesized in a multianvil apparatus at 14 GPa and 1550–1650 K under hydrous conditions. Single-crystal and polycrystal specimens of both phases were analyzed in the 1800–8500 cm?1 frequency region to determine the speciation, abundances, and partitioning behavior of the hydrous components in coexisting β-phase and olivine. β-phase spectra consistently show three distinct OH bands at 3329, 3580, and 3615 cm?1. OH concentrations range from 10000–65000 H/106 Si. A strong positive correlation of grain size and extent of transformation with OH concentration in the β-phase indicates that grain-growth and transformation rates are enhanced in a hydrous environment. Olivine spectra are variable, but consistently show a prominent broad-band absorbance representing molecular H2O, consistent with the infrared signature of the starting material. OH concentrations in olivine range from <300–1400 H/106 Si. The highest OH concentrations measured for olivine and the β-phase may represent solubility limits, in which case the OH solubility ratio between these two phases is approximately 1∶40. Where both phases coexist and are undersaturated with OH, the partitioning ratio of OH between them is about 1∶100. The large solubility contrast between olivine and the β-phase suggests a mechanism for hydrating the transition zone via olivine carried down in subducting slabs. Plumes impinging on an OH-rich upper transition region could cause H2 or H2O to be released upon transformation of the β-phase to olivine, resulting in initiation of secondary upwellings. If dissolution of OH weakens the β-phase, and if OH is present in the mantle, the region between 400–550 km could be a zone of low viscosity.  相似文献   
90.
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