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Schaefer CE do Amaral EF de Mendonça BA Oliveira H Lani JL Costa LM Fernandes Filho EI 《Environmental monitoring and assessment》2008,140(1-3):279-289
The relationships between soils attributes, soil carbon stocks and vegetation carbon stocks are poorly know in Amazonia, even
at regional scale. In this paper, we used the large and reliable soil database from Western Amazonia obtained from the RADAMBRASIL
project and recent estimates of vegetation biomass to investigate some environmental relationships, quantifying C stocks of
intact ecosystem in Western Amazonia. The results allowed separating the western Amazonia into 6 sectors, called pedo-zones:
Roraima, Rio Negro Basin, Tertiary Plateaux of the Amazon, Javari-Juruá-Purus lowland, Acre Basin and Rondonia uplands. The
highest C stock for the whole soil is observed in the Acre and in the Rio Negro sectors. In the former, this is due to the
high nutrient status and high clay activity, whereas in the latter, it is attributed to a downward carbon movement attributed
to widespread podzolization and arenization, forming spodic horizons. The youthful nature of shallow soils of the Javari-Juruá-Purus
lowlands, associated with high Al, results in a high phytomass C/soil C ratio. A similar trend was observed for the shallow
soils from the Roraima and Rondonia highlands. A consistent east–west decline in biomass carbon in the Rio Negro Basin sector
is associated with increasing rainfall and higher sand amounts. It is related to lesser C protection and greater C loss of
sandy soils, subjected to active chemical leaching and widespread podzolization. Also, these soils possess lower cation exchangeable
capacity and lower water retention capacity. Zones where deeply weathered Latosols dominate have a overall pattern of high
C sequestration, and greater than the shallower soils from the upper Amazon, west of Madeira and Negro rivers. This was attributed
to deeper incorporation of carbon in these clayey and highly pedo-bioturbated soils. The results highlight the urgent need
for refining soil data at an appropriate scale for C stocks calculations purposes in Amazonia. There is a risk of misinterpreting
C stocks in Amazonia when such great pedological variability is not taken into account. 相似文献
45.
通过监测和田地区生态修复项目实施后所取得生态效益的结果表明,生态修复项目实施后,由于项目区风速降低,温度和相对湿度的变化减少,提高了植被盖度,降低了风蚀量,促进了成土作用的进行,从而逐渐改善了土壤的理化性质。 相似文献
46.
铅冶炼区土壤重金属总量和有效态含量的函数分析 总被引:1,自引:0,他引:1
采集铅冶炼企业周边3 000 m范围内220个表层土壤样品,测定了有毒有害元素铅、镉、砷和汞的总量和有效态含量,探讨了它们之间的关系。结果表明:研究区土壤受到汞、砷、铅、镉的污染依次明显严重,土壤重金属的总量和有效态含量的变异系数均大于100%,土壤镉、铅、汞、砷的生物有效性系数平均值分别为25.9%、17.2%、0.58%、0.11%。土壤铅、镉和砷的总量与其有效态含量呈显著正相关(P0.001),而汞的总量与其有效态含量的相关性不显著(P0.05)。土壤铅和镉的总量和有效态含量可以用直线函数和幂函数表达,函数反推的有效态值和对应统计值的变异系数不大于10%。 相似文献
47.
建立了用加速溶剂萃取法(ASE)提取、气相色谱-串联质谱法分析土壤中20种有机氯农药的方法。用正己烷和丙酮(1∶1,V/V)的混合溶剂为提取剂,萃取温度100℃,压力1 500 psi,静态提取10 min,循环提取2次,提取液经石墨化碳黑固相萃取柱净化,浓缩后进行GC-MS/MS测定,外标法定量。试验结果表明,采用串联质谱多反应监测模式,降低了背景干扰,当取5 g土壤时,有机氯农药的检出限在0.1~3.0μg/kg之间,低浓度水平(8μg/kg)的基体加标回收率为70.3%~134%,相对标准偏差〈23%。测定方法背景干扰低,灵敏度高,适合土壤中20种有机氯农药残留的同时测定。 相似文献
48.
为了认识岩溶区石灰土含水介质中化学氧化联合生物降解去除燃油苯系物的效果,以汽油中的苯、甲苯、乙苯和二甲苯(BTEX)作为污染物,通过批实验研究过硫酸盐(PS)联合硝酸盐去除汽油BTEX的效果,并认识不同浓度乙醇(EtOH)存在时带来的影响及化学氧化与反硝化联合修复的可能性.结果表明,在35 d内各组的BTEX去除率均达到91.00%以上,PS化学氧化能有效地去除BTEX.在不含EtOH及含EtOH初始浓度为500和5000 mg·L-1的情况下,BTEX浓度在第65 d时分别为未检出、0.226 mg·L-1、0.243 mg·L-1,去除率分别为99.98%、99.00%、98.70%,其中,苯的去除率分别为99.98%、97.01%、93.32%.随着EtOH浓度的增加,苯的去除受到抑制,EtOH对BTEX的化学氧化具有阻碍作用.石灰土介质中高铁含量对PS具有活化能力,高含量有机质能促进PS分解,并导致pH值回升,出现反硝化作用和硫酸盐还原作用,有利于生物降解作用的恢复. 相似文献
49.
Z.A. Khan B.M. Misra K. Raghu 《Journal of environmental science and health. Part. B》2013,48(5):1015-1027
Abstract Interaction of lindane with silty loam and silty clay loam soils was studied in batch tests at 23, 30 and 37° C. Sorption experiments were carried out at four concentrations and for varying time of contact upto 72 hours. This was followed by desorption studies. No desorption was observed. The sorption data was analysed using sorption equations and evaluating the thermodynamic parameters. The sorption was found to be predominantly entropic in nature and a combined effect of adsorption and chemisorption. The effect of organic matter and other chemical and mineralogical constituents of soils has also been discussed. The sorption with single application of lindane with the two soil types indicates that the insecticide is less likely to reach groundwater. 相似文献
50.
Abstract The sorption and desorption characteristics of four herbicides (diuron, fluometuron, prometryn and pyrithiobac‐sodium) in three different cotton growing soils of Australia was investigated. Kinetics and equilibrium sorption and desorption isotherms were determined using the batch equilibrium technique. Sorption was rapid (> 80% in 2 h) and sorption equilibrium was achieved within a short period of time (ca 4 h) for all herbicides. Sorption isotherms of the four herbicides were described by Freundlich equation with an r2 value > 0.98. The herbicide sorption as measured by the distribution coefficient (Kd) values ranged from 3.24 to 5.71 L/kg for diuron, 0.44 to 1.13 L/kg for fluometuron, 1.78 to 6.04 L/kg for prometryn and 0.22 to 0.59 L/kg for pyrithiobac‐sodium. Sorption of herbicides was higher in the Moree soil than in Narrabri and Wee Waa soils. When the Kd values were normalised to organic carbon content of the soils (KoC), it suggested that the affinity of the herbicides to the organic carbon increased in the order: pyrithiobac‐sodium < fluometuron < prometryn < diuron. The desorption isotherms were also adequately described by the Freundlich equation. For desorption, all herbicides exhibited hysteresis and the hysteresis was stronger for highly sorbed herbicides (diuron and prometryn) than the weakly sorbed herbicides (fluometuron and pyrithiobac‐sodium). Hysteresis was also quantified as the percentage of sorbed herbicides which is not released during the desorption step ω = [nad / nde ‐1] x 100). Soil type and initial concentration had significant effect on ω. The effect of sorption and desorption properties of these four herbicides on the off‐site transport to contaminate surface and groundwater are also discussed in this paper. 相似文献