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31.
The population structures of Buccinum tsubai and Neptunea constricta were compared using partial sequences of the mitochondrial COI gene. B. tsubai included four genetically distinguishable subpopulations (Hokkaido, Yamagata-Toyama, Yamato Bank, and San’in), which is consistent with the results of our previous study using mitochondrial 16SrRNA sequences. The genetic structure of N. constricta was also clear, but the lineage sorting corresponding to the geographical distribution was not as clear as that of B. tsubai. The difference between the genetic structures of these two species might be due to a difference in either their dispersal abilities or the historic distribution patterns in the Sea of Japan. The fossil record and nested clade analyses support the latter alternative. The four subpopulations of B. tsubai are estimated to have diverged 0.42–1.46 million years ago, providing support for the existence of intermediate water of normal salinity and oxygen concentration capable of sustaining B. tsubai between the low-salinity surface water and anoxic deep water during the Pleistocene glacial periods. The genetic diversity of the Yamato Bank subpopulation of B. tsubai was lower than that of the other subpopulations, which is likely attributable to the small size of the Yamato Bank subpopulation.  相似文献   
32.
Soil and sediments collected at a former chlor‐alkali plant in coastal Georgia (United States), revealed the presence of PCDF concentrations as great as 82.3 ng/g, dry wt. PCDF congener profile in soil was typical of “chlorine pattern”; with elevated proportions of OCDF and HpCDF. Concentrations of PCDFs declined gradually by 44‐fold at a distance of about 500 m along the contamination gradient. Of PCDDs/DFs, 2,3,7,8‐substituted PCDFs accounted for 94–98% of the TCDD‐like activity, which declined by 25‐fold, corresponding with the reduction of total PCDF concentrations. Concentrations of PCDDs in sediments were as great as 17 ng/g, with an elevated contribution from OCDD. The magnitude of decline in PCDD concentrations with distance from the source was less pronounced than that for PCDFs. PBDDs and PBDFs were not detected. Polybrominated biphenyl ether (PBBE) and monobromo‐heptachloro dibenzo‐p‐dioxins and dibenzofurans (PXDDs/DFs) were found, though, at low concentrations. Their spatial distribution was similar to those of PCDDs.  相似文献   
33.
Organophosphoric acid triester (OPE) concentration levels in water and bottom sediment at the Osaka North Port Sea-Based Solid Waste Disposal Site were investigated, and the behavior of OPEs in the water environment of the waste disposal site was examined. The more highly water-soluble OPEs were frequently detected in raw water. Of the OPEs detected, TCEP and TCPP showed very high concentrations (1.0–90 μg/l), followed by TEP (0.3–10 μg/l) > TBXP (0.8–6.3 μg/l) > TDCPP (0.6–6.2 μg/l) > TBP (0.2–1.5 μg/l) > TPP (<0.1 μg/l). Most OPEs detected in water were eluted from the disposal waste to the water phase immediately and behaved as dissolved forms with no distribution in suspended solids (SS). On the other hand, the less water-soluble OPEs, such as TCP or TEHP, were detected in bottom sediment but hardly at all in water samples. All OPEs were detected at the waste disposal site, within which their concentration levels were uniform. It appeared that the less water-soluble OPEs were present as SS-associated forms and behaved in line with the floating surface sludge at the bottom. Received: July 6, 1998 / Accepted: February 25, 1999  相似文献   
34.
Ozawa H  Kawaguchi H  Okuyama Y  Arakawa H 《Ambio》2012,41(Z2):149-150
The first example of a ruthenium sensitizer (TUS-22) having a natural dye, bisdemethoxycurcumin, as a ligand has been synthesized. The dye-sensitized solar cell based on this novel dye showed 5.8% conversion efficiency under AM 1.5 (100 mW/cm(2)) irradiation.  相似文献   
35.
Perfluorooctanesulfonate (PFOS) and perfluorooctanoate (PFOA) have been recognized as emerging environmental pollutants because of their ubiquitous occurrence in the environment, biota, and humans. PFOS and PFOA have been detected in water in Japan. Nevertheless, occurrence of PFOS and PFOA in potable water from municipal water treatment plants is not clearly known. We analyzed PFOS and PFOA in raw and tap water samples collected from 14 drinking water treatment plants in winter and summer seasons in Osaka to determine the concentrations of PFOS and PFOA in raw and potable tap water samples. PFOS and PFOA were detected in all raw water samples. Concentration ranges of PFOS and PFOA in raw water were 0.26-22 ng/l and 5.2-92 ng/l, respectively. Whereas the concentrations PFOS in raw water from Osaka were similar to those in other areas in Japan, the concentrations of PFOA were higher than in other areas. Concentration ranges of PFOS and PFOA in potable tap water were 0.16-22 ng/l and 2.3-84 ng/l, respectively. There were positive correlations between PFC concentrations in raw water and tap water samples. Therefore, the removal efficiency of PFCs by the present water treatment may be low. Based on the current action value reported by U.S. Environmental Protection Agency, PFOA concentrations found in tap water in Osaka is not expected to pose health risks.  相似文献   
36.
To reutilize molten slag derived from an ash melting process, the lead volatilization mechanism under reducing conditions was investigated. Reducing conditions were established by introducing a CO-CO2-N2 gas mixture to the reactor or by adding graphite to the molten slag prior to the experiments. As samples, two types of simulated molten slag composed of CaO-SiO2-Al2O3 mixed with PbO were used and the lead volatilization behavior was studied at 1773 K. It was found that the lead volatilization rate increased on increasing the amount of reducing agent for both graphite and the CO-CO2 gas mixture. For the CO-CO2 reducing gas mixture, this increase was mainly attributed to PbO conversion to Pb. For the addition of graphite, the increase in lead volatilization ratio was considered to partially result from PbO conversion to Pb and partially from a reaction of graphite with SiO2 yielding volatile SiO. The volatile SiO gas was then emitted from the furnace, which brought about a reduction in the SiO2 content of the slag. As a result, the slag viscosity decreased, which led to an enhancement of the lead volatilization ratio.  相似文献   
37.
The effect of different light regimes on the development of sexual maturity and body composition (carbon, nitrogen, lipid and protein) of Antarctic krill, Euphausia superba, was studied over 12 weeks under laboratory conditions. Krill were exposed to light-cycle regimes of variable intensity to simulate Southern Ocean summer, autumn and winter conditions, respectively using: (1) continuous light (LL; 200 lux max), (2) 12-h light and 12-h darkness (LD 12:12; 50 lux max), and (3) continuous darkness (DD). The sexual maturity of female and male krill exposed to LL and LD 12:12 showed an accelerated succession of external maturity stages during the experimental period, while krill exposed to continuous darkness showed no changes in external maturity during the course of the study. Changes in the maturity development of krill between the different light regimes are reflected in changes in body composition. Krill exposed to LL and LD 12:12 showed an increase in lipid utilization, indicating that the development of external maturation may be fuelled preferentially by lipid reserves. In contrast, values of total lipid content of krill held under continuous darkness indicated an unchanged lipid catabolism during the course of the study. Thus, the maturity development of krill was affected either directly or indirectly by the different simulated light conditions. Based on these results, and observations on the effects of simulated light regimes on feeding and metabolic rates of krill available from a previous study, we suggest that the Antarctic light regime is an essential cue governing the seasonal cycle of krill physiology and maturity, and highlight the importance of this environmental factor in the life history of krill.  相似文献   
38.
The photocatalytic degradation of monochlorobenzene using titanium dioxide aqueous suspensions was performed under solar-simulated irradiation. The effects of concentration of monochlorobenzene, amount of titanium dioxide and pH of solution on the degradation were examined. The intermediates identified were three monochlorophenols, chlorohydroquinone and hydroxy-hydroquinone.  相似文献   
39.
Degradation of organophosphoric esters (OPEs) in leachate from a sea-based solid waste disposal site was investigated by laboratory experiment. Aryl-phosphates, tricresyl phosphate and triphenyl phosphate, in leachate rapidly decreased to less than the detection limit within 20 days under aerobic condition, suggesting high biodegradability. These phosphates also decreased in sterilized leachate, which suggested a contribution to degradation by reactions (adsorption and chemical degradation) with chemicals in the leachate. Concerning alkyl-phosphates, tributyl phosphate decreased rapidly after one week, which is considered to have been caused by biodegradation. Tris-2-ethylhexyl phosphate and tris-2-butoxyethyl phosphate decreased slowly in all samples but that of sterilized distilled water. This however, suggested contribution of biodegradation because the velocity of decrease in the leachate was higher than in control samples. Among chloro alkylphosphates, decrease of tris-2-chloroethyl phosphate and tris-dichloropropyl phosphate were observed though it was not obvious whether by biodegradation or not. Decrease of tris-2-chloropropyl phosphate (TCPP) was not observed for 80 days suggesting that TCPP remains in the leachate over a long period of time. Except for aryl-phosphates decrease of OPEs was not observed under anaerobic condition. It was considered that the composition ratio and the behavior of OPEs in leachate in the field reflects the biological and chemical degradation as well as the chemical properties of OPEs.  相似文献   
40.
We examined larval mesopelagic fish assemblages, their distribution, and seasonal occurrence patterns in the Kuroshio–Oyashio transition region of the western North Pacific where complex hydrographic structures are observed due to the confluence of the Kuroshio Extension and Oyashio current. Larvae of the dominant families Myctophidae, Gonostomatidae, Bathylagidae, Sternoptychidae, and Phosichthyidae were represented by 31 species or types belonging to 24 genera. Based on species composition analysis using the Morishita–Horn similarity index, five assemblages were recognized: Oyashio, Spring Transition, Summer Transition, Kuroshio, and Slope Water assemblages. The distribution patterns of these assemblages corresponded closely with hydrographic structures such as position of the Oyashio and Kuroshio Extension fronts, warm core rings and streamers. Spring Transition (April) and Summer Transition (July–October) assemblages were the most important larval assemblages in the transition region. Larval abundances were low during late autumn and winter. The Spring Transition and Summer Transition assemblages were composed of subtropical, transitional, subarctic, and slope-water species, suggesting the importance of the transition region as nursery grounds of mesopelagic fishes of various origins from subarctic to subtropical waters. Larval fish transport by the Kuroshio, Oyashio, and Tsugaru Warm currents into the transition region is discussed.  相似文献   
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