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111.
长江上游攀西——六盘水地区是个资源富集的“金三角”。通过交通先行,加快资源开发,对增强21世纪经济发展后劲意义重大。但生态环境恶化,急需加强保护。  相似文献   
112.
雷州半岛与海南岛砖红壤养分比较研究罗凯(广东省徐闻县农村工作委员会,徐闻524100)ComparisonofNutrientsContentofLatosolsinLeizhouPeninsulaandHainanIsland¥LuoKai(Rur...  相似文献   
113.
查清中低产田的面积、分布与开发条件是制定农业综台开发规划的重要依据。采用按公里网布设的农业资源动态监测系统,开展对耕地不同产量水平的面积与分布的动态监测,其方法具有准确、简便和实用的特点。  相似文献   
114.
分析了润滑油基础油在储运过程中,油品质量可能产生的不良变化和对周围环境造成的危害.针对这些危害提出了解决的对策.  相似文献   
115.
Luo Y  Hui D  Zhang D 《Ecology》2006,87(1):53-63
The capability of terrestrial ecosystems to sequester carbon (C) plays a critical role in regulating future climatic change yet depends on nitrogen (N) availability. To predict long-term ecosystem C storage, it is essential to examine whether soil N becomes progressively limiting as C and N are sequestered in long-lived plant biomass and soil organic matter. A critical parameter to indicate the long-term progressive N limitation (PNL) is net change in ecosystem N content in association with C accumulation in plant and soil pools under elevated CO2. We compiled data from 104 published papers that study C and N dynamics at ambient and elevated CO2. The compiled database contains C contents, N contents, and C:N ratio in various plant and soil pools, and root:shoot ratio. Averaged C and N pool sizes in plant and soil all significantly increase at elevated CO2 in comparison to those at ambient CO2, ranging from a 5% increase in shoot N content to a 32% increase in root C content. The C and N contents in litter pools are consistently higher in elevated than ambient CO2 among all the surveyed studies whereas C and N contents in the other pools increase in some studies and decrease in other studies. The high variability in CO2-induced changes in C and N pool sizes results from diverse responses of various C and N processes to elevated CO2. Averaged C:N ratios are higher by 3% in litter and soil pools and 11% in root and shoot pools at elevated relative to ambient CO2. Elevated CO2 slightly increases root:shoot ratio. The net N accumulation in plant and soil pools at least helps prevent complete down-regulation of, and likely supports, long-term CO2 stimulation of C sequestration. The concomitant C and N accumulations in response to rising atmospheric CO2 may reflect intrinsic nature of ecosystem development as revealed before by studies of succession over hundreds to millions of years.  相似文献   
116.
Accumulation and phytoavailability of benzo[a]pyrene in an acid sandy soil   总被引:1,自引:0,他引:1  
Effects of benzo[a]pyrene (B[a]P) on ryegrass (Lolium perenne L.) growth, plant accumulation and dissipiation of B[a]P in a red sandy soil (Hapli-Udic Argosol) were studied in a pot experiment. The plants were grown for 61 days in soil spiked with B[a]P at 0, 12.5, 25 and 50 mg kg−1. Control pots without plants were also set up. Soil extractable B[a]P, plant shoot and root biomass, and concentrations of B[a]P in plant shoots and roots were determined. Ryegrass biomass was increased by addition of B[a]P and root B[a]P concentrations were significantly correlated with B[a]P application rate, but no such correlation was found for shoot B[a]P concentrations. This indicates that B[a]P enhanced the growth of the ryegrass. The extractable B[a]P concentration in the planted soil was significantly lower than that in the unplanted control soil at the rate of 50 mg B[a]P kg−1. This indicates that ryegrass may help to dissipate B[a]P in soil at concentrations over 50 mg kg−1 soil although the mechanism for this is not understood.  相似文献   
117.
TiO2/SiO2催化剂光催化降解罗丹明B的表观动力学   总被引:2,自引:0,他引:2  
尤宏  姚杰  罗薇楠  陈平 《环境科学》2006,27(11):2154-2158
采用多孔硅胶为载体的TiO2/SiO2光催化剂,建立了三相内循环流化床光催化氧化体系,并以罗丹明B染料为典型污染物,研究其降解规律.通过对罗丹明B降解过程的表观动力学研究,发现在该体系中罗丹明B的降解并不符合Langmuir-Hinshelwood反应动力学模型.实验表明,其降解反应动力学符合双曲型模式,即降解率的倒数1/X和时间的倒数1/t成线性关系.反应速率常数与反应物初始浓度无关,与光源强度和相对体积能量吸收速率成正比.将不同实验条件下的罗丹明B的降解率实测值与模型计算值相比较,二者能很好吻合,平均相对偏差仅为3.25%.  相似文献   
118.
The extraction of K+ and SiO2 from silicate minerals by Bacillus mucilaginosus in liquid culture was studied in incubation experiments. B. mucilaginosus was found to dissolve soil minerals and mica and simultaneously release K+ and SiO2 from the crystal lattices. In contrast, the bacterium did not dissolve feldspar. B. mucilaginosus also produced organic acids and polysaccharides during growth. The polysaccharides strongly adsorbed the organic acids and attached to the surface of the mineral, resulting in an area of high concentration of organic acids near the mineral. The polysaccharides also adsorbed SiO2 and this affected the equilibrium between the mineral and fluid phases and led to the reaction toward SiO2 and K+ solubilization. These two processes led to the decomposition of silicate minerals by the bacterium.  相似文献   
119.
Chen B  Duan JC  Mai BX  Luo XJ  Yang QS  Sheng GY  Fu JM 《Chemosphere》2006,63(4):652-661
The occurrence of alkylphenols (APs) was investigated in surface water and sediments from the Pearl River Delta and adjacent northern South China Sea. Most of the water samples contained detectable amounts of APs, ranging up to 0.628 microg l(-1) for nonylphenol (NP) and 0.068 microg l(-1) for octylphenol (OP). APs were found in all of the sediment samples with concentrations ranging from 59 to 7808 microg kg(-1) for NP and from 1 to 93 microg kg(-1) for OP. The Zhujiang River showed the highest concentrations of APs in both water and sediments. Significant decrease of APs concentrations going from the Zhujiang River to the Shiziyang River was observed. The Xijiang River contained concentrations of APs slightly higher in water but relatively lower in sediments than the Lingding Bay, which might be attributed to their different hydrodynamic and sedimentary characteristics. There was a decreasing trend of APs in water from the rivers to the estuary and further to the sea on the whole. In the Lingding Bay and its outer waters, concentrations of APs in sediments increased to a maximum and then decrease seaward, which was consistent with the distribution trend of the sediment organic carbon contents. Linear regression analyses showed the concentrations of APs were markedly correlated with the sediment organic carbon contents, indicating that the sediment organic carbon is an important factor controlling the levels of APs in sediments.  相似文献   
120.
Photocatalytic oxidation of triclosan   总被引:1,自引:0,他引:1  
Yu JC  Kwong TY  Luo Q  Cai Z 《Chemosphere》2006,65(3):390-399
In the spring of 2003, there was an outbreak of the severe respiratory syndrome (SARS) in Hong Kong. Health concerns have thus triggered an increased and predominant use of various types of household cleansing agents such as triclosan (5-chloro-2-(2,4-dichlorophenoxy)phenol). However, it has been reported recently that triclosan could be photochemically converted to toxic 2,8-dichlorodibenzo-p-dioxin (2,8-Cl(2)DD) in the environment. It is therefore necessary to develop environmentally friendly methods for the treatment of triclosan. To this end, photocatalytic degradation of triclosan in aqueous solution was conducted using TiO(2) (Degussa P25) under irradiation of UV light (lambda < 365 nm). It was found that triclosan could be degraded by this approach. Hydrogen peroxide was added to enhance the degradation process, and the optimal initial hydrogen peroxide concentration for triclosan degradation was 0.005% (w/v). Product identification indicated that triclosan oxidation occurred at its phenol moiety and yielded quinone and hydroquinone intermediates. The formation of a dichlorophenol intermediate in triclosan degradation suggested bond-breaking of the ether linkage occurred during the process. Moreover, no chlorinated dibenzo-p-dioxin congener was detected. These findings confirm that the photocatalytic degradation of triclosan is an environmentally friendly process.  相似文献   
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