辛硫磷降解菌XSP-1的分离、鉴定及其降解特性研究

从农药厂污泥中分离到1株能以辛硫磷为唯一碳源生长的细菌, 命名为XSP-1.根据其生理生化特征和16S rRNA基因序列相似性分析, 将该菌株初步鉴定为戴尔福特菌属(Delftia sp.). 该菌株能在7 h内完全降解100　mg/L的辛硫磷. XSP-1降解辛硫磷的最适pH为7.0, 最适温度为35℃, 降解速率与初始接种量呈正相关, 该菌株对甲基对硫磷、毒死蜱、杀螟硫磷也有较好的降解能力. 根据已报道有机磷农药降解基因mpd的保守序列设计引物, 未从该菌株中扩增到目标条带, 但是该菌株是否带有新的有机磷农药降解基因仍需要进一步研究.     

Sorption of 1-naphthol by plant cuticular fractions

The contribution of aliphatic-rich plant biopolymer to sorption of hydrophobic organic compounds is significantly important because of their preservation and accumulation in the soil environment,but sorption mechanism is still not fully understood.In this study, sorption of 1-naphthol by plant cuticular fractions was examined to better understand the contributions of respective fraction.Toward this end,cuticular materials were isolated from the fruits of tomato by chemical method.The tomato cuticle sheet consisted of waxes (6.5 wt%),cuticular monomer (69.5 wt%),and polysaccharide (24.0 wt%).Isotherms of l-naphthol to the cuticular fractions were nonlinear (N value (0.82-0.90)) at the whole tested concentration ranges.The KodKow ratios for bulk cuticle (TC1),dewaxed cuticle (TC2),cutin (TC4),and desugared cuticle (TC5) were larger than unity,suggested that tomato bulk cuticle and cutin are much powerful solption medium.Sorption capability of cutin (TC4) was 2.4 times higher than the nonsaponifiable fraction (TC3).The 1-naphthol interactions with tomato cuticular materials were governed by both hydrophobic-type interactions and polar (H-bonding) interactions. Removal of the wax and polysaccharide materials from the bulk tomato cuticle caused a significant increase in the sorption ability of the cuticular material.There was a linear negative trend between K_(oc) values and the amount of polysaccharides or fraction's polarities ((N O)/C);while a linear positive relationship between K_(oc) values and the content of cutin monomer (linear R~2=0.993) was observed for present in the cuticular fractions.Predominant sorbent of the hydrophobic organic compounds (HOCs) in the plant cuticular fraction was the cutin monomer,contributing to 91.7% of the total sorption of tomato bulk cuticle.     

离子液体双水相气浮溶剂浮选分离/富集水样中的盐酸多西环素研究

建立了以亲水性离子液体1-丁基-3-甲基咪唑四氟硼酸[Bmim]BF4和Na H2PO4形成的二元双水相作为气浮溶剂分离/富集水样中盐酸多西环素的新方法,并采用紫外分光光度法对盐酸多西环素进行测定。考察了离子液体的初始加入量、盐的种类及浓度、p H值、浮选时间及N2流速等因素对体系浮选分离盐酸多西环素的影响。结果表明,改变离子液体和无机盐的加入量,会使体系的富集倍数发生变化,从而使体系的浮选效率和浓集系数发生变化;随浮选时间增加,体系的浮选效率先增加后略微下降;过大或过小的N2流速都会使体系对盐酸多西环素的浮选效率降低;而p H值对体系浮选盐酸多西环素影响不大。当[Bmim]BF4溶液加入量为3 m L、Na H2PO4加入量为25 g(质量分数为33.3%)、气浮时间为40 min、气浮速率为50 m L/min时,体系的浮选效率最高,可达95.8%,浓集系数可达23.95,此时体系的p H值为4.38。与离子液体双水相萃取(ILATPE)相比,该方法的优点在于不仅有较高的浮选率、浓集系数,还有效减少了离子液体的用量,同时操作更简单、环境友好。     

GM（1， 1）正弦模型修补气温监测缺失数据的探讨

目的建立预测精度较好的大气温度监测缺失数据修补的方法和模型。方法采用正弦函数对GM(1,1)标准模型进行修正,建立分段的GM(1,1)正弦修正模型对缺失数据进行修补。以万宁试验站某天监测的温度日记时值数据为试验数据,同时建立GM(1,1)标准模型、GM(1,1)时序修正模型和GM(1,1)正弦修正模型,对比分析各模型的修补误差,确立较好的修补模型。结果从模型的拟合效果分析,GM(1,1)标准模型和GM(1,1)正弦修正模型的拟合性最好,GM(1,1)时序修正模型的拟合性相对较差一些;从预测精度上分析,GM(1,1)标准模型和GM(1,1)时序修正模型预测修补效果差,平均相对误差分别达到22.54%和17.70%,而GM(1,1)正弦修正模型预测修补的平均误差仅为3.14%,得到了较大的改进,预测效果好。结论正弦修正模型能很好地修补缺失数据,其修补效果比时序修正模型和标准模型都要好。     

Effectiveness of China's National Forest Protection Program and nature reserves

There is profound interest in knowing the degree to which China's institutions are capable of protecting its natural forests and biodiversity in the face of economic and political change. China's 2 most important forest‐protection policies are its National Forest Protection Program (NFPP) and its national‐level nature reserves (NNRs). The NFPP was implemented in 2000 in response to deforestation‐caused flooding. We undertook the first national, quantitative assessment of the NFPP and NNRs to examine whether the NFPP achieved its deforestation‐reduction target and whether the NNRs deter deforestation altogether. We used MODIS data to estimate forest cover and loss across mainland China (2000–2010). We also assembled the first‐ever polygon dataset for China's forested NNRs (n = 237, 74,030 km² in 2000) and used both conventional and covariate‐matching approaches to compare deforestation rates inside and outside NNRs (2000–2010). In 2000, 1.765 million km² or 18.7% of mainland China was forested (12.3% with canopy cover of ≥70%)) or woodland (6.4% with canopy cover <70% and tree plus shrub cover ≥40%). By 2010, 480,203 km² of forest and woodland had been lost, an annual deforestation rate of 2.7%. Forest‐only loss was 127,473 km² (1.05% annually). In the NFPP provinces, the forest‐only loss rate was 0.62%, which was 3.3 times lower than in the non‐NFPP provinces. Moreover, the Landsat data suggest that these loss rates are overestimates due to large MODIS pixel size. Thus, China appears to have achieved, and even exceeded, its target of reducing deforestation to 1.1% annually in the NFPP provinces. About two‐thirds of China's NNRs were effective in protecting forest cover (prevented loss 4073 km² unmatched approach; 3148 km² matched approach), and within‐NNR deforestation rates were higher in provinces with higher overall deforestation. Our results indicate that China's existing institutions can protect domestic forest cover.     

天山乌鲁木齐河源1号冰川气溶胶可溶性离子观测与分析研究

基于2003年、2004年和2007年3年内共采集的155个气溶胶样品的分析测试,探讨了天山乌鲁木齐河源1号冰川区气溶胶中可溶性离子的组成及年际变化特征,并对其可能来源进行了分析.结果表明,气溶胶可溶性离子平均浓度为2.759μg·m-3,化学组成以NO-3、SO2-4、Ca2+和CO2-3为主,冰川区大气环境呈碱性.可溶性离子总质量浓度年际变化特征为2007年2004年2003年,主要离子组成没有发生明显变化,但单一离子浓度变化不尽相同,其原因主要与沙尘活动的强弱有关.Ca2+、Na+、Mg2+、CO2-3和Cl-主要可能来自陆源矿物,而NO-3和NH+4很大程度上以人为源为主;并且发现,SO2-4和K+可能同时受陆地源与人类活动来源的影响.通过气团轨迹聚类分析得出,冰川区大气主要受来自西南方、西方及西北方3个方向气团的控制,这些气团均经过伊犁河谷或阿拉山口到达冰川区,其中,在距地面2000 m以下高度传输的气团会带来大量的沙尘物质,影响冰川区大气环境.     

Thermal hazard assessment for synthesis of 3-methylpyridine-N-oxide

The exothermic oxidation of 3-methylpyridine with hydrogen peroxide was analyzed by Reaction Calorimeter (RC1e) in semi-batch operation. Heat releasing rate and heat conversion were studied at different operating conditions, such as reaction temperature, feeding rate, the amount of catalyst and so on. The thermal hazard assessment of the oxidation was derived from the calorimetric data, such as adiabatic temperature rise (ΔT_ad) and the maximum temperature of synthesis reaction (MTSR) in out of control conditions. Along with thermal decomposition of the product, the possibility of secondary decomposition under runaway conditions was analyzed by time to maximum rate (TMR_ad). Also, risk matrix was used to assess the risk of the reaction. Results indicated that with the increase of the reaction temperature, the reaction heat release rate increased, while reaction time and exotherm decreased. With the increase of feeding time, heat releasing rate decreased, but reaction time and exotherm increased. With the amount of the catalyst increased, heat releasing rate increased, reaction time decreased and exothermic heat increased. The risk matrix showed that when the reaction temperature was 70 &#176;C, feeding time was 1 h, and the amount of catalyst was 10 g and 15 g, respectively, the reaction risk was high and must be reduced.     

A 1-dodecanethiol-based phase transfer protocol for the highly efficient extraction of noble metal ions from aqueous phase

A 1-dodecanethiol-based phase-transfer protocol is developed for the extraction of noble metal ions from aqueous solution to a hydrocarbon phase, which calls for first mixing the aqueous metal ion solution with an ethanolic solution of 1-dodecanethiol, and then extracting the coordination compounds formed between noble metal ions and1-dodecanethiol into a non-polar organic solvent. A number of characterization techniques,including inductively coupled plasma atomic emission spectroscopy, Fourier transform infrared spectroscopy, and thermogravimetric analysis demonstrate that this protocol could be applied to extract a wide variety of noble metal ions from water to dichloromethane with an efficiency of 96%, and has high selectivity for the separation of the noble metal ions from other transition metals. It is therefore an attractive alternative for the extraction of noble metals from water, soil, or waste printed circuit boards.