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71.
72.
Marine Biology - The combined effects of temperature and salinity on the rate of oxygen consuption by the estuarine crab Panopeus herbstii Milne-Edwards (Crustacea: Decapoda: Xanthidae) were... 相似文献
73.
Jan Kupec Kateřina Charvátová Milan Navrátil Vojtěch Křesálek Martina Křesálková 《Journal of Polymers and the Environment》2003,11(3):93-100
Most native polymers used in processing and application technologies are admittedly disposable from the environment in a biologic manner, but products possess low mechanical strength. One of the paths to increasing this attribute (if feasible) is their cross-linking, which may, however, affect their readiness to biodegradation. In the presented work this condition was observed on the example of waste protein (Hykol B) cross-linking by means of glutardialdehyde and glyoxal. Degree and course of cross-linking were determined through impedance spectroscopy. The objective of this work also was to obtain data for constructing a sensor capable of following the cross-linking course in real time, for potential industrial application of Hykol in continuous production. Impedance spectroscopy proved to be applicable even to this kind of material marked by considerable water content and exhibiting relatively high electric conductivity; so far it had been used only for materials of low conductivity. An aqueous environment inoculated with digested anaerobic sludge from a municipal wastewater treatment plant was selected for modeling anaerobic conditions. The relation was studied between cross-linking degree given by content of cross-linking agent (determined by impedance spectroscopy) and biodegradation degree under anaerobic conditions. It was confirmed that network density as given by quantity of added agent not only reduced breakdown degree but also slowed the course of the process. This fact is particularly obvious with cross-linking by means of glyoxal; network density is thus dependent on type of employed substance, which affect type and structure of created network. That not merely forms an obstacle during polymer swelling and dissolution but also prevents access of bacteria to source of metabolized organic carbon. 相似文献
74.
H. Ozaki K. Sharma C. Phanuwan K. Fukushi C. Polprasert 《Journal of Material Cycles and Waste Management》2003,5(1):0031-0038
This paper deals with the present scenario of hazardous waste management practices in Thailand, and gives some insights into
future prospects. Industrialization in Thailand has systematically increased the generation of hazardous waste. The total
hazardous waste generated in 2001 was 1.65 million tons. It is estimated that over 300 million kg/year of hazardous waste
is generated from nonindustrial, community sources (e.g., batteries, fluorescent lamps, cleansing chemicals, pesticides).
No special facilities are available for handling these wastes. There are neither well-established systems for separation,
storage, collection, and transportation, nor the effective enforcement of regulations related to hazardous wastes management
generated from industrial or nonindustrial sectors. Therefore, because of a lack of treatment and disposal facilities, these
wastes find their way into municipal wastewaters, public landfills, nearby dump sites, or waterways, raising serious environmental
concern. Furthermore, Thailand does not have an integrated regulatory framework regarding the monitoring and management of
hazardous materials and wastes. In addition to the absence of a national definition of hazardous wastes, limited funding has
caused significant impediments to the effective management of hazardous waste. Thus, current waste management practices in
Thailand present significant potential hazards to humans and the environment. The challenging issues of hazardous waste management
in Thailand are not only related to a scarcity of financial resources (required for treatment and disposal facilities), but
also to the fact that there has been no development of appropriate technology following the principles of waste minimization
and sustainable development. A holistic approach to achieving effective hazardous waste management that integrates the efforts
of all sectors, government, private, and community, is needed for the betterment of human health and the environment.
Received: February 26, 2001 / Accepted: October 11, 2002 相似文献
75.
Roger K. Raufer 《Natural resources forum》1997,21(3):209-219
Recent research has suggested that health damage from air pollution—most notably from inhalable particulate matter and lead—is a serious concern in many cities in developing countries. A comparative risk assessment conducted in Cairo in 1994 found these two pollutants to be especially worrisome, and an analysis of the potential economic benefits associated with controlling these pollutants suggests that their economic damage is significant. Control strategies to reduce ambient pollutant levels are under development, with point source controls on major industrial facilities—especially in the secondary lead smelling industry—a cost-effective initial step. 相似文献
76.
Liang Chen Syed H. Imam Sherald H. Gordon Richard V. Greene 《Journal of Polymers and the Environment》1997,5(2):111-117
Starch-PVOH cast films were prepared with and without crosslinking agent (hexamethoxymethylmelamine) in the absence of plasticizer.
Moisture absorption in films without crosslinking agent at a low relative humidity was similar to that of PVOH and increased
as the relative humidity increased. Films with crosslinking agent showed moisture absorption linearly proportional to the
relative humidity. Significant improvement in resistance to water disintegration for crosslinked starch-PVOH films was observed.
While the tensile strength decreased with increased relative humidity, crosslinking significantly improved the tensile strength.
Increased PVOH content improved elongation of films even when the relative humidity was 80% or higher. Biodegradation studies
revealed that the degradation rate was negatively correlated with the PVOH content in films and crosslinking generated more
converged degradation curves.
Names are necessary to report factually on available data; however, the USDA neither guarantees nor warrants the standard
of the product, and the use of the name by USDA implies no approval of the product to the exclusion of others that may also
be suitable. 相似文献
77.
Davey L. Jones John F. Farrar Kevin K. Newsham 《Water, Air, & Soil Pollution: Focus》2004,4(6):169-175
Amino acids constitute one of the largest inputs of organic nitrogen (N) to most polar soils and have been hypothesized to be important in regulating vegetational succession and productivity in Arctic ecosystems. Our understanding of amino acid cycling in these soils, however, is poor. The aim of this study was to investigate the size and rate of turnover of the amino acid pool in a range of Arctic and Antarctic soils. Our results indicate that in polar soils with either high or low ornithogenic inputs the amino acid pool is small in comparison to the inorganic N pool (NO–3 and NH+4). The free amino acid pool constituted only a small proportion of the total dissolved organic nitrogen (DON) pool in these soils. Here we show that these low concentrations may be due to rapid use by the soil microbial community in both Arctic and Antarctic soils. The turnover of the amino acid pool in soil was extremely rapid, with a half-life ranging from 2 to 24 h, indicating that this N pool can be turned over many hundred times each summer when polar soils are frequently unfrozen. The implications of amino acids in N cycling and plant and microbial nutrition are discussed. 相似文献
78.
A solution containing 35SO4 2- and 3H2O was applied to four plots (5 × 5 m) in a boreal coniferous forest in the Laflamme Lake watershed, Québec, under two contrasting conditions: in summer (plots 1 and 2), and on the snowpack before snowmelt (plots 3 and 4). The transit of both these tracers in the soil solution was then followed through a network of soil lysimeters located at different depths. Four months after the summer application, 3H2O had infiltrated the whole soil profile at plot 1, while 35SO4 2- was only observed in the LFH and Bhf horizons. A 35SO4 2- budget calculated from mid-August to November indicated that 89 and 10.6% of the added 35SO4 2- was retained within the LFH and the Bhf layers, respectively. Fifteen months later, the added 35SO4 2- was distributed in the following proportions within the soil horizons: LFH (73.7%), Bhf (11.8%) and Bf (12.8%), for a total retention rate of 98.3%. The superficial penetration of 3H2O at plot 2 was indicative of a major lateral water movement that prevented the calculation of a 35SO4 2- budget. This situation also was observed at plot 4 during snowmelt. At plot 3, 3H2O moved freely through the soil profile and a significant fraction of the added 35SO4 2- reached the B horizons, where it was presumably adsorbed on aluminum (Al) and ferric (Fe) oxides. The 35SO4 2- budget for plot 3 from March to November indicated that 87% of the added 35SO4 2- was retained within the soil profile, with most being retained in the B horizons (LFH = 33.1%, Bhf = 33.1%, Bf = 20.8%). The contrasting retention patterns of 35SO4 2- within the soil profile following the summer addition and snowmelt likely was caused by the contrastingsoil temperatures and soil solution residence times within the differentsoil layers. The persistence of 35SO4 2- in the soil solution of the entire profile long after the initial tracer infiltration, and the relative temporal stability of specific activity of SO4 2-, point to the establishment of an isotopic equilibrium between the added 35SO4 and the active S-containing reservoirs within a given soil horizon. Overall, the results clearly illustrate the very strong potential for 35SO4 2- retention and recycling in forest soils. 相似文献
79.
80.
Davey L. Jones John F. Farrar Kevin K. Newsham 《Water, Air, & Soil Pollution: Focus》2005,4(6):169-175
Amino acids constitute one of the largest inputs of organic nitrogen (N) to most polar soils and have been hypothesized to be important in regulating vegetational succession and productivity in Arctic ecosystems. Our understanding of amino acid cycling in these soils, however, is poor. The aim of this study was to investigate the size and rate of turnover of the amino acid pool in a range of Arctic and Antarctic soils. Our results indicate that in polar soils with either high or low ornithogenic inputs the amino acid pool is small in comparison to the inorganic N pool (NO? 3 and NH+ 4). The free amino acid pool constituted only a small proportion of the total dissolved organic nitrogen (DON) pool in these soils. Here we show that these low concentrations may be due to rapid use by the soil microbial community in both Arctic and Antarctic soils. The turnover of the amino acid pool in soil was extremely rapid, with a half-life ranging from 2 to 24 h, indicating that this N pool can be turned over many hundred times each summer when polar soils are frequently unfrozen. The implications of amino acids in N cycling and plant and microbial nutrition are discussed. 相似文献