紫外辐射增加对春小麦根际土壤微生物种群数量的影响

研究了大田栽培和自然光条件下,模拟紫外辐射（UB-B,280－315nm）增加对春小麦根际土壤微生物种群数量的影响。UV－B辐射能显著降低细菌总数以及放线菌和真菌数量;UV－B辐射对好氧性自生固氮菌、亚硝酸细菌、反硝化细菌、好氧性纤维素分解菌和解磷细菌数量也有显著的影响,但这种影响具有生育期之间的差异,春小麦根际土壤微生物种群数量与土壤营养成分有关。     

电子设备太阳辐射模拟试验分析与探讨

阐述了太阳辐射对电子产品的影响,介绍了试验的种类和进行选择的标准,重点分析了日辐射强度及其谱能分布、试验温度、湿度和风速等基本参数的确定依据和有关试验技术,并对太阳辐射试验模拟设备的研制提出设计要求,为我国自行研制非标环境试验设备提供了依据.     

微波技术在废水处理中的应用

文章简述了微波直接辐射和微波再生技术在废水处理中的应用.指出了微波技术在废水处理中存在的问题,并对其发展前景进行了展望.     

油罐扬沸火灾防治模拟实验研究

分析扬沸火灾形成的3个基本物理条件,给出扬沸三角形的概念,提出通过破坏3个基本条件中任一条件来抑制扬沸火灾发生的构想。为解决其防治问题建立小尺度油罐扬沸火灾防治模拟实验台,用沸石和双列盘管式冷却法对扬沸火灾防治进行了实验研究;通过对比两种方法施加前后的油层、油水界面、水层温度和火焰辐射,发现双列盘管式冷却法和沸石能有效地抑制扬沸的形成和降低扬沸的危害程度。从机理上分析,小尺度油罐扬沸火灾的防治方法可为扬沸火灾的防治提供一定的理论依据。     

Effect of modulated microwave radiation on human EEG asymmetry

This study is aimed to investigation of the effect of modulated 450 MHz microwave radiation on the EEG inter-hemispheric asymmetry. Ten cycles of the microwave exposure (1 min off and 1 min on) at fixed modulation frequency were applied on two groups of healthy volunteers. The first group of 13 subjects was exposed to microwave radiation modulated at 14 Hz and the second group of 15 subjects at 40 Hz frequency. The peak specific absorption rate (SAR) average over 1 g was 0.303 W/kg. Differences in SAR between hemispheres were up to 20 dB. Rod antenna was located from the left side of the head. Differences of relative changes in EEG energy between symmetric channels FP1–FP2, T3–T4, P3–P4 and O1–O2 in exposed and sham conditions were analysed. The results showed increase in EEG energy from the left side caused by microwave exposure. Statistical analysis done for the whole group of subjects didn’t reveal significant differences in inter-hemispheres asymmetry between exposed and sham conditions. However, statistical analysis performed for individual subjects detected significant differences in asymmetry caused by exposure for 15–35% of individuals.     

多相光催化反应器辐射能模型的建立与验证

采用双通量模型模拟了管式三相流化床光催化反应器中辐射能分布和局部体积能量吸收速率,并采用负载型TiO2/SiO2光催化剂进行了实验验证,考察了液相介质、通气量及催化剂浓度对光辐射强度和体积能量吸收速率的影响.实验结果表明,实验数据和模型计算值能够较好吻合,蒸馏水做液相介质时,可将气液鼓泡流看成单一的连续相,催化剂浓度越...     

基于开源GIS的长江流域晴日辐射反演

以开源GIS软件GRASS为平台,首次通过辐射过程模型r.sun和编程语言Shell实现长江流域500 m分辨率的晴日辐射反演（包括直接辐射、散射辐射和反射辐射）,为了解长江流域辐射时空分布规律和相关宏观气候、生态建模奠定基础。结论如下：（1）精度验证表明,晴日辐射反演结果较理想;相关晴日指数的误差指标MPE、MAPE和RMSE分别为37%、75%和64%,r.sun模型可进一步用于中国其它区域;（2）长江流域晴日辐射年均日值为2424±245 MJ/(m2·d),其各组分差异显著,直接、散射、反射辐射分别占总辐射的842%、156%和02%;（3）晴日辐射空间分布梯度明显,沿三级地形阶梯向东辐射值及变异逐渐减小,海拔变化引起的大气衰减因素在决定晴日辐射分布时起重要作用;（4）晴日辐射季节分布不对称,月际变化总体呈倒“U”形分布;直接辐射和散射辐射变化趋势基本一致,但二者比例随大气浑浊度的变化波动剧烈。     

Cell size dependence of additive versus synergetic effects of UV radiation and PAHs on oceanic phytoplankton

Polycyclic Aromatic Hydrocarbons’ (PAHs) toxicity is enhanced by the presence of ultraviolet radiation (UVR), which levels have arisen due to the thinning of the ozone layer. In this study, PAHs’ phototoxicity for natural marine phytoplankton was tested. Different concentrations of a mixture of 16 PAHs were added to natural phytoplankton communities from the Mediterranean Sea, Atlantic, Arctic and Southern Oceans and exposed to natural sunlight received in situ, including treatments where the UVR bands were removed. PAHs’ toxicity was observed for all the phytoplankton groups studied in all the waters and treatments tested, but only for the pico-sized group a synergetic effect of the mixture and UVR was observed (p = 0.009). When comparing phototoxicity in phytoplankton from oligotrophic and eutrophic waters, synergy was only observed at the oligotrophic communities (p = 0.02) where pico-sized phytoplankton dominated. The degree of sensitivity was related to the trophic degree, decreasing as Chlorophyll a concentration increased.     

Data driven modelling of vertical atmospheric radiation

In the Czech Hydrometeorological Institute (CHMI) there exists a unique set of meteorological measurements consisting of the values of vertical atmospheric levels of beta and gamma radiation. In this paper a stochastic data-driven model based on nonlinear regression and on nonhomogeneous Poisson process is suggested. In the first part of the paper, growth curves were used to establish an appropriate nonlinear regression model. For comparison we considered a nonhomogeneous Poisson process with its intensity based on growth curves. In the second part both approaches were applied to the real data and compared. Computational aspects are briefly discussed as well. The primary goal of this paper is to present an improved understanding of the distribution of environmental radiation as obtained from the measurements of the vertical radioactivity profiles by the radioactivity sonde system.     

Rapid determination of dichlorodiphenyltrichloroethane and its main metabolites in aqueous samples by one-step microwave-assisted headspace controlled-temperature liquid-phase microextraction and gas chromatography with electron capture detection

A rapid and sensitive analytical method for the determination of dichlorodiphenyltrichloroethane (DDT) and its main metabolites in environmental aqueous samples has been developed using one-step microwave-assisted headspace controlled-temperature liquid-phase micro-extraction (MA-HS-CT-LPME) technique coupled with gas chromatography-electron-capture detection (GC-ECD). In this study, the one-step extraction of DDT and its main metabolites was achieved by using microwave heating to accelerate the evaporation of analytes into the controlled-temperature headspace to form a cloudy mist vapor zone for LPME sampling. Parameters influencing extraction efficiency were thoroughly optimized, and the best extraction for DDT and its main metabolites from 10-mL aqueous sample at pH 6.0 was achieved by using 1-octanol (4-μL) as the LPME solvent, sampling at 34 °C for 6.5 min under 249 W of microwave irradiation. Under optimum conditions, excellent linear relationship was obtained in the range of 0.05-1.0 μg/L for 1-dichloro-2,2-bis-(p′-chlorophenyl)ethylene (p,p′-DDE), 0.1-2.0 μg/L for o,p′-DDT, 0.15-3.0 μg/L for 1,1-dichloro-2,2-bis-(p′-chlorophenyl)ethane (p,p′-DDD) and p,p′-DDT, with detection limits of 20 ng/L for p,p′-DDE, and 30 ng/L for o,p′-DDT, p,p′-DDD and p,p′-DDT. Precision was in the range of 3.2-11.3% RSD. The proposed method was validated with environmental water samples. The spiked recovery was between 95.5% and 101.3% for agricultural-field water, between 94% and 99.7% for sea water and between 93.5% and 98% for river water. Thus the established method has been proved to be a simple, rapid, sensitive, inexpensive and eco-friendly procedure for the determination of DDT and its main metabolites in environmental water samples.