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161.
采用室内恒温培养研究了施肥对不同农田土壤微生物活性的影响。结果表明,在红壤、水稻土和潮土中,土壤微生物量、土壤酶活性大小顺序均为有机肥配施无机肥处理>单施有机肥处理>单施无机肥处理,但对脲酶来说,其活性大小顺序为有机肥配施无机肥处理>单施无机肥处理>单施有机肥处理。从土壤类型来看,土壤微生物量碳、氮和土壤酶活性大小以水稻土最大,潮土次之,红壤最小。3种土壤的微生物量、土壤酶活性在培养的45~60d之间分别达到最大值,以后逐渐下降。部分单施无机肥处理的土壤微生物量、土壤酶活性最大值比单施有机肥处理、有机肥配施无机肥处理提前15d。相关分析表明,有机肥配施无机肥处理及单施有机肥处理,3种土壤的土壤微生物量碳、氮与土壤过氧化氢酶、转化酶、蛋白酶、脲酶及速效养分呈显著或极显著的相关性;单施无机肥处理中,土壤微生物量碳、氮与土壤过氧化氢酶、蔗糖转化酶、蛋白酶、脲酶显著或极显著相关,与部分速效养分相关不显著。  相似文献   
162.
过氧化氢酶活性及活性抑制的紫外分光光度测定   总被引:66,自引:3,他引:66  
在体内实验条件下,测定了鲤鱼肝脏过氧化氢酶的活性。实验结果表明,过氧化氢酶的紫外分光光度法是可靠的,活性抑制结果表明,对-二硝基苯对鲤鱼肝脏过氧化氢酶无有明显的抑制作用。鲤鱼肝脏过氧化氢酶可作为一项指标用于生态毒理学研究。  相似文献   
163.
不同土地利用方式下Cd、Pb复合污染对土壤酶活性的影响   总被引:1,自引:1,他引:1  
为探寻合理的土地利用方式,减轻重金属污染,以上海市崇明岛为研究对象,结合室内盆栽模拟试验,研究了不同土地利用方式下Cd、Pb复合污染对土壤酶活性的影响,以期为合理规划土地功能和提高土壤健康程度提供科学依据。试验结果表明,农田、生活用地等受人类活动影响较明显的地区,其土壤酶活性低于湿地、林地、河道旁等人为扰动较少且水分充足的地区;土壤脲酶、磷酸酶和脱氢酶活性两两之间呈显著正相关(P<0.01),且土壤脲酶对Cd、Pb较敏感;土壤有机质与土壤酶活性呈显著正相关(P<0.05);Cd、Pb复合污染在低含量(Cd:0~1mg.kg-1;Pb:0~60mg.kg-1)时对土壤酶活性表现为促进作用,而高含量(Cd:0~20mg.kg-1;Pb:0~100mg.kg-1)时则表现为抑制作用。  相似文献   
164.
为解决载体內部微孔孔径在废水生物膜法中缺乏选型依据的问题,采用5种孔径(0.6~4 mm)聚氨酯海绵生物载体构建了SBBR,考察了载体内微孔孔径对生物膜特性(MLSS、EPS、DHA)及废水处理效果的影响,分析了载体内部微孔孔径与生物膜特性的相关性。结果表明:载体内微孔孔径与MLVSS、MLSS呈显著负相关,而与PN、PS、EPS和f呈显著正相关;高生物量使小孔径载体(0.6 mm,1 mm)在反应器运行前中期拥有最佳的废水处理效果,同时过多的生物膜在微孔环境中会堵塞内部的通道和空穴,进而抑制传质,使生物膜活性(DHA、f )降低;而大孔径载体(4 mm)内部传质快、水力剪切作用强,加速生物膜解吸脱落速率,促进了生物膜活性的提高与EPS(主要是TB-EPS)的释放,但同样限制了生物膜量的增长。相较而言,中等孔径载体(2 mm,3 mm)适宜的微孔不仅能维持适量的微生物量,还能保持良好的生物膜结构和活性,为生物膜反应器提供良好的长期运行条件和处理效果。  相似文献   
165.
The maximum specific methanogenic activity (SMA) of a sludge originating from a brewery wastewater treatment plant on the degradation of glucose was investigated at various levels of sulfate on a specific loading basis. Batch experiments were conducted in serum bottles at pH 7 and 35℃. A comparison of the values indicates that the SMA of this mixed culture was increased and reached its highest level of 0.128 g CH4 gas COD/(g VSS.d) when biomass was in contact with sulfate at a ratio of 1:0.114 by weight.  相似文献   
166.
李明  梁湘  骆健美  周明华 《环境科学学报》2015,35(10):3078-3087
本研究以天津泰达污水处理厂污泥浓缩间的污泥为接种物,启动并运行了微生物燃料电池(MFCs).从富集的阳极生物膜上分离得到了一株纯培养的微生物菌种,命名为P2-A-5.研究发现,菌株P2-A-5的16S rDNA序列与菌株Kocuria rhizophila DC2201具有100%的同源性,结合该菌的形态特征和生理生化实验,将其归属为嗜根考克氏菌(Kocuria rhizophila).通过化学剂处理、底物种类和浓度的优化,进一步提高其在微生物燃料电池中的产电性能.结果表明,菌株K.rhizophila P2-A-5经0.5 mg·L-1溶菌酶处理45 min后,接种到以2.0 g·L-1海藻糖为底物的阳极液中运行MFCs,其功率密度达到314.8 m W·m-2,比优化前(74.9 m W·m-2)提高了320.3%.这是首次对K.rhizophila种内微生物产电性能及其在微生物燃料电池中应用的报道,其成果对于丰富产电微生物的多样性,挖掘更多具有高电化学活性的微生物菌种,提高其产电性能具有重要的理论意义.  相似文献   
167.
Twenty microfungal isolates were collected from diseased fruiting bodies of Agaricus bisporus sampled from Serbian mushroom farms during 2003–2007. Based on morphological characteristics and pathogenicity tests, the isolates were identified as Cladobotryum dendroides. The isolates of C. dendroides and A. bisporusF56 and U3 were tested for sensitivity to several selected fungicides in vitro. C. dendroides isolates were found to be more sensitive to prochloraz manganese and flusilazole + carbendazim than to the other fungicides tested (EC50 values were 0.09 and 0.11 mg L? 1, respectively) and weakly resistant to thiophanate-methyl (EC50 values ranged between 6.53 and 12.09 mg L? 1). Selectivity indexes of the tested fungicides on both C. dendroidesand A. bisporusindicated that thiophanate-methyl, cyproconazole + carbendazim and flusilazole + carbendazim had much less selective fungitoxicity than benomyl, carbendazim and prochloraz manganese.  相似文献   
168.
Abstract

Leaching, downward mobility and persistence of tebufenozide was investigated under laboratory conditions in columns packed with forest litter and soil, after fortification with the analytical grade material (purity > 99.6%) and with two commercial formulations, RH‐5992 2F (aqueous flowable) and RH‐5992 ES (emulsion suspension). Two types of litter and soil were used: one type with relatively high amounts of sand and the other with high amounts of clay.

The concentrations eluted in the leachates were lower when the analytical material (dissolved in acetone) was used for fortification, than when the two formulations (diluted with water) were used. The amount leached was higher for RH‐5992 2F than for RH‐5992 ES. The type of substrate, i.e., sandy or clay type, had only marginal influence on the amounts eluted in the leachates. Downward movement of tebufenozide from the top 2‐cm layer to the untreated middle and bottom layers (3‐cm segments) was consistently lower when the analytical material was used for fortification, than when the two formulations were used. Downward movement was higher for RH‐5992 2F than for RH‐5992 ES. Persistence of tebufenozide in substrates, maintained under submerged conditions for 70 days after leaching, indicated an initial 2‐week lag period prior to the onset of degradation. Formulation‐related differences were observed in the half‐life (DT50) values. When the analytical material was used for fortification, the DT50 ranged from ca 54 to 59 d. However, when the formulations were used for fortification, the DT50 showed a higher range, i.e., from ca 62 to 67 d for RH‐5992 2F and ca 70 to 80 d for RH‐5992 ES. Formulation ingredients appear to have caused enhanced adsorption of tebufenozide onto the substrates, thus delaying degradation.  相似文献   
169.
The noxious effects of low or effective dose exposure to single or mixed pesticides on macrophage activity and the lymphohematopoietic organs were investigated. Male Wistar rats were orally exposed to dichlorvos, dicofol, endosulfan, dieldrin and permethrin, either as single or combined mixtures during a 28-day study containing eight groups: one group received a semipurified diet (non-treated); two groups received a semipurified diet containing low dose mixture (dieldrin 0.025 mg/kg, endosulfan, 0.6 mg/kg, dicofol 0.22 mg/kg, dichlorvos 0.23 mg/kg, permethrin 5 mg/kg) or an effective dose mixture (dichlorvos 2.3 mg/kg, dicofol 2.5 mg/kg, endosulfan 2.9 mg/kg, dieldrin 0.05 mg/kg and permethrin 25.0 mg/kg), respectively; the other five groups received a semipurified diet containing each single pesticide in effective doses. At sacrifice, the thymus, spleen, mesenteric lymph nodes, Payer's patches and bone marrow were removed for histological analysis. Peritoneal macrophages were obtained to determine the phagocytosis and spreading indexes and tumoral necrosis factor alpha (TNF-α), nitric oxide (NO) and H2O2 production. Exposure to pesticide mixtures did not alter the percentage of macrophage phagocytosis and spreading, TNF-α production or the NO and H2O2 release when compared to the non-treated group. Neither was there any apparent evidence that a pesticide mixture at low or effective doses altered the histological structure of the lymphohematopoietic organs. The findings indicate that short-term treatment with pesticide mixtures did not induce an apparent immunotoxic effect in male Wistar rats.  相似文献   
170.
Trichoderma species, the causal agents of green mould disease, induce great losses in Agaricus bisporus farms. Fungicides are widely used to control mushroom diseases although green mould control is encumbered with difficulties. The aims of this study were, therefore, to research in vitro toxicity of several commercial fungicides to Trichoderma isolates originating from Serbian and Bosnia-Herzegovina farms, and to evaluate the effects of pH and light on their growth. The majority of isolates demonstrated optimal growth at pH 5.0, and the rest at pH 6.0. A few isolates also grew well at pH 7. The weakest mycelial growth was noted at pH 8.0–9.0. Generally, light had an inhibitory effect on the growth of tested isolates. The isolates showed the highest susceptibility to chlorothalonil and carbendazim (ED50 less than 1 mg L?1), and were less sensitive to iprodione (ED50 ranged 0.84–6.72 mg L?1), weakly resistant to thiophanate-methyl (ED50 = 3.75–24.13 mg L?1), and resistant to trifloxystrobin (ED50 = 10.25–178.23 mg L?1). Considering the toxicity of fungicides to A. bisporus, carbendazim showed the best selective toxicity (0.02), iprodione and chlorothalonil moderate (0.16), and thiophanate-methyl the lowest (1.24), while trifloxystrobin toxicity to A. bisporus was not tested because of its inefficiency against Trichoderma isolates.  相似文献   
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