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151.
Swails Erin Yang X. Asefi S. Hergoualc’h K. Verchot L. McRoberts R. E. Lawrence D. 《Mitigation and Adaptation Strategies for Global Change》2019,24(4):575-590
Mitigation and Adaptation Strategies for Global Change - Carbon dioxide (CO2) emissions from Southeast Asia peatlands are contributing substantially to global anthropogenic emissions to the... 相似文献
152.
153.
Jochen Stutz Kam Weng Wong Laura Lawrence Luke Ziemba James H. Flynn Bernhard Rappenglück Barry Lefer 《Atmospheric environment (Oxford, England : 1994)》2010,44(33):4099-4106
Radical chemistry in the nocturnal urban boundary layer is dominated by the nitrate radical, NO3, which oxidizes hydrocarbons and, through the aerosol uptake of N2O5, indirectly influences the nitrogen budget. The impact of NO3 chemistry on polluted atmospheres and urban air quality is, however, not well understood, due to a lack of observations and the strong impact of vertical stability of the boundary layer, which makes nocturnal chemistry highly altitude dependent.Here we present long-path DOAS observations of the vertical distribution of the key nocturnal species O3, NO2, and NO3 during the TRAMP experiment in Summer 2006 in Houston, TX. Our observations confirm the altitude dependence of nocturnal chemistry, which is reflected in the concentration profiles of all trace gases at night. In contrast to other study locations, NO3 chemistry in Houston is dominated by industrial emissions of alkenes, in particular of isoprene, isobutene, and sporadically 1,3-butadiene, which are responsible for more than 70% of the nocturnal NO3 loss. The nocturnally averaged loss of NOx in the lowest 300 m of the Houston atmosphere is ~0.9 ppb h?1, with little day-to-day variability. A comparison with the daytime NOx loss shows that NO3 chemistry is responsible for 16–50% of the NOx loss in a 24-h period in the lowest 300 m of the atmosphere. The importance of the NO3 + isoprene/1,3-butadiene reactions implies the efficient formation of organic nitrates and secondary organic aerosol at night in Houston. 相似文献
154.
Christian Seigneur Elpida Constantinou Mary Fend Leonard Levin Lawrence Graft Chris Whipple 《Journal of the Air & Waste Management Association (1995)》2013,63(10):823-830
Abstract The inclusion of non-detected chemicals in a health risk assessment may lead, in some cases, to estimated risks that exceed regulatory thresholds, because one must use the detection limit or half of the detection limit. This study presents a methodology which will allow one to estimate appropriate detection limits by conducting a health risk assessment prior to the source sampling program. The advantages and shortcomings of various levels of detail in the risk assessment to determine those detection limits are discussed. The application of the methodology is demonstrated with a case study of the potential health effects of power plant stack emissions. 相似文献
155.
Michel P. Bonin William L. Flower Ronald F. Renzi Lawrence W. Peng 《Journal of the Air & Waste Management Association (1995)》2013,63(11):902-907
Abstract Optical measurements of particle size and concentration were made at the chromium plating tank and exhaust system at a commercial hexavalent chromium plating facility. Particles were examined at three locations in the exhaust system: 1) directly at the hexavalent chromium plating bath surface, 2) at the exit of a cyclone separator located in the exhaust system approximately three to four meters downstream of the bath, and 3) in the exhaust stack, downstream of the induced draft fan and all abatement devices. Particle diameters at the bath surface ranged from 0.3 to 25 μm. Downstream of the cyclone exit and mesh pad filters, particle top sizes were approximately 5 and 0.7 mm, respectively. On a mass basis, the collection efficiency of all abatement devices was 99.997%. Assuming that droplets in the flow consist primarily of water and chromium, correcting the total particle mass flow against water content gives a chromium emission rate of 64,000 μg/hr, which compares favorably with a value of 77,000 μg/hr measured with EPA methods. This initial agreement, which should be validated through additional measurements over a broad range of flow conditions, raises the possibility of continuous monitoring for chromium metal emissions using particle size/mass as a surrogate. 相似文献
156.
Nehzat Motallebi Hien Tran Bart E. Croes Lawrence C. Larsen 《Journal of the Air & Waste Management Association (1995)》2013,63(7):876-888
Abstract This paper analyzes day-of-week variations in concentrations of particulate matter (PM) in California. Because volatile organic compounds (VOCs) and oxides of nitrogen (NOx) are not only precursors of ozone (O3) but also of secondary PM, it is useful to know whether the variations by day of week in these precursors are also evident in PM data. Concentrations of PM ≤10 μm (PM10) and ≤2.5[H9262]m in aerodynamic diameter (PM2.5) were analyzed. PM concentrations exhibit a general weekly pattern, with the maximum occurring late in the workweek and the minimum occurring on weekends (especially Sunday); however, this pattern does not prevail at all sites and areas. PM nitrate (NO3 -) data from Size Selective Inlet (SSI) samplers in the South Coast Air Basin (SoCAB) tend to be somewhat lower on weekends compared with weekdays. During 1988–1991, the weekend average was lower than the weekday average at 8 of 13 locations, with an average decrease of 1%. During 1997–2000, the weekend average was lower than the weekday average at 10 of 13 locations, with an average decrease of 6%. The weekend averages are generally lower than weekday averages for sulfates, organic carbon, and elemental carbon. Because heavy-duty trucks typically represent a major source of elemental carbon, the weekend decrease in heavy-duty truck traffic may also result in a decrease in ambient elemental carbon concentrations. 相似文献
157.
Howard P. Gates Jr. Lawrence A. Goldmuntz 《Journal of the Air & Waste Management Association (1995)》2013,63(9):891-892
Carboxyhemoglobin (COHb) levels in blood are principally due to inhalation of carbon monoxide, although a low level (approximately 0.3%) of COHb is endogenous. A carboxyhemoglobin level above 1.5 % in non-smokers indicates exposure to CO in excess of the 10 mg/m3 air quality standard established under the Clean Air Act Amendments of 1970. In most major U.S. cities, automobile emissions constitute the principal source of CO; in Chicago, according to EPA estimates,1 light duty vehicles are responsible for 69.3% of all CO emissions. Thus as new automobiles incorporating emission controls enter the automotive fleet and older, emission-uncontrolled automobiles are phased out, ambient CO concentrations should decline and corresponding reductions in blood carboxyhemoglobin levels of nonsmokers can be expected. 相似文献
158.
Large quantities of atmospheric aerosols with compositions SO4 =, NO3 ? and NH4 + have been detected in highly industrialized areas. The major portions of aerosol products are the results of energyrelated fuel combustion. Both microphysical and macrophysical processes are considered in investigating the time dependent evolution of the saturation spectra of condensation nuclei associated with both polluted and clean atmospheres during the time periods of advection fog formation. The results show that the condensation nuclei associated with a polluted atmosphere provide more favorable conditions than condensation nuclei associated with a clean atmosphere to produce dense advection fog, and that attaining a certain degree of supersaturation is not necessarily required for the formation of advection fog with condensation nuclei associated with a polluted atmosphere for monodisperse distribution. 相似文献
159.
Thomas McCurdy Michael P. Zelenka Philip M. Lawrence Robert M. Houston Robert Burton 《Atmospheric environment (Oxford, England : 1994)》1999,33(30):488
This article presents data on ambient concentrations of selected acidic aerosols at four existing monitoring sites in the Pittsburgh PA metropolitan area. The data were collected by staff of the Allegheny County Health Department, Division of Air Quality during the summer and fall of 1993. The sampling protocol was focused on obtaining 24 h-average ammonia, ammonium, acidic sulfates, and particle strong acids data on a 2 to 3 day cycle. The data were obtained using Harvard University School of Public Health's “Short-HEADS” annular denuder sampling train. The Pittsburgh area is of interest because it is downwind of a major regional source of sulfur and nitrogen emissions from coal-burning power plants: the Ohio River Valley. The data presented here indicate that ground-level concentrations of acidic aerosols in Pittsburgh are highly correlated spatially and that many pollutants are higher on days when ground-level wind direction vectors indicate that wind is coming from the southwest rather than from the Pittsburgh source area itself. The monitoring site that is most upwind of the Pittsburgh source area – South Fayette – has particle strong acid levels about twice those of sites closer in to the Pittsburgh central business district. 相似文献
160.