Identification of Tsuga Germplasm by Morphological Characters and RAPD Markers

Germplasm collection is important to preserve and maximize genetic diversity for germplasm conservation. Tsuga dumosa （ D. Don） Eichler in Engler ＆ Prantl. and T. chinensis var. forrestii （Downie） Silba germplasm was collected from three localities in China： Mt. Yulong, Wenfeng Temple and Mt. Dishiergu, Yunnan Province. Accessions were identified based on morphological characters and RAPD markers. The shapes of the apices and margins of needles were examined, and the length and width of needles, cones and seeds from accessions of mature plants were used to compare the morphological differences and to identify the germplasm. Molecular markers generated by randomly amplified polymorphic DNA （RAPD） were also used to characterize the taxa. Although the clustering based on RAPD markers was inconsistent with the morphological characters of the needles, based on the overall morphological characters and on RAPD markers, the accessions from Mt. Yulong and Wenfeng Temple were identified as T. chinertsis var. forrestii, and those from Mt. Dishiergu identified as T. dumosa. Taxonomic identification of the accessions was made based on morphology and by RAPD markers concurred. The results indicate that the shapes of the apices and margins of needles particularly from young plants could not be used as a possible key to identify T. dumosa and T. chinertsis var. forrestii. Fig 6, Tab 3, Ref24     

Effects of Earthworm Invasion on Plant Species Richness in Northern Hardwood Forests

Abstract:  The invasion of non-native earthworms ( Lumbricus spp.) into a small number of intensively studied stands of northern hardwood forest has been linked to declines in plant diversity and the local extirpation of one threatened species. It is unknown, however, whether these changes have occurred across larger regions of hardwood forests, which plant species are most vulnerable, or with which earthworm species such changes are associated most closely. To address these issues we conducted a regional survey in the Chippewa and Chequamegon national forests in Minnesota and Wisconsin (U.S.A.), respectively. We sampled earthworms, soils, and vegetation, examined deer browse in 20 mature, sugar-maple-dominated forest stands in each national forest, and analyzed the relationship between invasive earthworms and vascular plant species richness and composition. Invasion by Lumbricus was a strong indicator of reduced plant richness in both national forests. The mass of Lumbricus juveniles was significantly and negatively related to plant-species richness in both forests. In addition, Lumbricus was a significant factor affecting plant richness in a full model that included multiple variables. In the Chequamegon National Forest earthworm mass was associated with higher sedge cover and lower cover of sugar maple seedlings and several forb species. The trends were similar but not as pronounced in Chippewa, perhaps due to lower deer densities and different earthworm species composition. Our results provide regional evidence that invasion by Lumbricus species may be an important mechanism in reduced plant-species richness and changes in plant communities in mature forests dominated by sugar maples.     

香港及珠三角地区MODIS高分辨率气溶胶光学厚度的反演

为了有效解决地区性和城市范围内的气溶胶分布并反演陆地上气溶胶的性质,一种针对中分辨率成像光谱辐射计(MODIS)的气溶胶反演新算法应运而生.本文首先通过改良的最小反射率技术(MRT)来确定季节性的地表反射率和利用瑞利通道辐射率中解析出大气上气溶胶的反射率来估计气溶胶的反射系数.结果表明,MRT地表反射率的图像和MODIS地表反射系数的产品(MOD09)有很好的契合度.两者的相关系数高达0.9.此外,考虑到不同气溶胶的光学性质和太阳观测组合对计算辐射传输的影响,本研究还制定了全面广泛的差算表(LUT).由此产生的卫星500m分辨率的气溶胶光学厚度(AOT)和香港太阳光度计(AERONET)及MicrotopsⅡ观测资料的相关系数r分别为0.96和0.87(相伴概率值P<0.0001).该研究证明了城区高分辨率气溶胶反演的可行性,还能帮助研究气溶胶的分布和城区大气瞬态污染的影响.此外,MODIS 500m分辨率的气溶胶光学厚度图像还可用于研究跨境气溶胶,使定位珠江三角洲区域污染源变得可行.     

胶州湾海泊河口水域水体的吸收、荧光特性与溶解有机碳的实验研究

实验研究了海泊河废水及其河口区水体的光学性质以及溶解有机碳(DOC)浓度,分析了光吸收系数(aCDOM)、最大荧光强度与DOC的关系.结果表明,海水中aCDOM在1.81～3.51 m-1内,平均值为2.39 m-1;而废水样品的aCDOM在0.59～16.23 m-1内,平均值为3.35 m-1.海水中aCDOM、光吸收指数斜率系数(S)、最大荧光强度以及DOC浓度都小于废水中相应的参数.水体中aCDOM、最大荧光强度以及DOC浓度三者之间均存在较好的线性关系.胶州湾东部海区海水中CDOM主要来源于海泊河排放的废水,由于水动力和潮汐作用较强而很快扩散,它们的浓度很快降低,在海泊河附近海区没有明显的积累.     

Urea hydrolysis and recovery of nitrogen and phosphorous as MAP from stale human urine

Laboratory-scale tests for magnesium ammonium phosphate(MAP)precipitation following urea hydrolysis of human urine were conducted using orthogonal experiment design.The effects of initial pH,temperature and the volumetric ratios of stale urine to fresh urine,on urea hydrolysis in urine were studied to determine the final hydrolysis time to recover most nitrogen from separated human urine by MAP.With a volumetric ratio of stale to fresh urine>10% and at temperature≥20℃,urea hydrolysis could be completed i...     

以一种黏土矿物材料为非均相类芬顿催化剂对甲基橙的降解

为实现以甲基橙为代表的偶氮类染料的高效降解,采用一种黏土矿物材料——Quantum Energy? Radiating Material（下称QE）为催化剂,系统分析了其在非均相类芬顿反应中的催化剂协同静态吸附作用,并考察了不同因素对甲基橙去除效果的影响,同时基于降解过程中Fe2+和总Fe析出量（以ρ计）、·OH等的变化过程,探讨了QE降解甲基橙的作用机制.结果表明,QE对甲基橙具有良好的吸附作用,同时,其作为非均相类芬顿催化剂对甲基橙的降解受到pH、温度、c（H₂O₂）、催化剂投加量等因素的影响.优化后的降解条件:初始ρ（甲基橙）为50 mg/L、QE投加量为5 g/L、c（H₂O₂）为100 mmol/L、pH为2、温度为60℃,在该条件下反应40 min后,甲基橙的去除率可达到99%.以叔丁醇作为·OH淬灭剂,随着c（叔丁醇）的增高,反应体系中甲基橙的去除率随之下降,说明·OH在该体系甲基橙降解中起重要作用;对在反应过程中Fe2+和总Fe析出量的监测数据表明,体系中QE对甲基橙的降解为均相芬顿反应、非均相芬顿反应和吸附作用协同作用的结果.研究显示,以QE为催化剂,通过吸附协同催化氧化作用可以有效处理含甲基橙的染料废水.      

生物炭在农业增产和污染治理中的应用

生物炭(biochar)作为重要的碳汇、土壤重要的改良剂以及污染物有效地吸附剂受到了国内外研究人员的普遍关注。在阅读近几年国内外关于生物炭在农业增产和污染方面文献的基础上,作者总结了生物炭应用规律并提出一些未来研究的展望。表述如下:生物炭具有多孔性和巨大的表面积,它能够增加土壤的持水量、增加对营养元素的吸附以减少其流失并改善土壤的结构,此外生物炭本身含有丰富的营养元素并能够缓慢释放以供作物吸收,因此生物炭能改善土壤肥力并增加农作物产量。同时,生物炭巨大的吸附功能可以降低重金属和有机污染物在土壤及污水中的活性,起到降低污染物浓度的作用。因此生物炭在农业增产和减少污染方面有巨大的潜力。但是,到目前为止,对于生物炭很多的作用机制还未搞清楚,对不同种类生物炭性状、生物质在高温热解过程中内部化学成分和结构的变化、长期定位实验以及危害方面还应加强研究。对此,研究人员应该结合当地情况,尽多的用当地主要的动植物废料来生产生物炭以达到当地农业增产和治理污染的目的;其次,增加长期定位试验,找到适合当地的生物炭种类及其生产条件;另外还应增加对我国新疆、西藏等土壤贫瘠的偏远地区的研究,使当地的土壤更大程度的被利用以改善当地人民的生活;最后,当地政府及相关部门应该加大对生物炭研究的支持,使生物炭早日被普遍运用,造福百姓。     

Carbonaceous aerosols in PM10 and pollution gases in winter in Beijing

An intensive observation of organic carbon (OC) and element carbon (EC) in PM10 and gaseous materials (SO2, CO, and O3,) was conducted continuously to assess the characteristics of wintertime carbonaceous aerosols in an urban area of Beijing, China. Results showed that the averaged total carbon (TC) and PM10 concentrations in observation period are 30.2±120.4 and 172.6±198.3 μ/m3, respectively. Average OC concentration in nighttime (24.9±19.6 μ/m3) was 40% higher than that in daytime (17.7±10.9 μ/m3). Average EC concentrations in daytime (8.8±15.2 μ/m3) was close to that in nighttime (8.9±15.1 μ/m3). The OC/EC ratios in nighttime ranging from 2.4 to 2.7 are higher than that in daytime ranging from 1.9 to 2.0. The concentrations of OC, EC, PM10 were low with strong winds and high with weak winds. The OC and EC were well correlated with PM10, CO and SO2, which implies they have similar sources. OC and EC were not well correlated with O3. By considering variation of OC/EC ratios in daytime and night time, correlations between OC and O3, and meteorological condition, we speculated that OC and EC in Beijing PM10 were emitted as the primary particulate form. Emission of motor vehicle with low OC/EC ratio and coal combustion sources with high OC/EC ratio are probably the dominant sources for carbonaceous aerosols in Beijing in winter. A simple method was used to estimate the relative contribution of sources to carbonaceous aerosols in Beijing PM10. Motor vehicle source accounts for 80% and 68%, while coal combustion accounts for 20% and 32% in daytime and nighttime, respectively in Beijing. Averagely, the motor vehicle and coal combustion accounted for 74% and 26%, respectively, for carbonaceous aerosols during the observation period. It points to the motor vehicle is dominant emission for carbonaceous aerosols in Beijing PM10 in winter period, which should be paid attention to control high level of PM10 in Beijing effectively.     

Effects of low temperature on aluminum(III) hydrolysis: Theoretical and experimental studies

In this study, the effects of low temperature on aluminum(III) (Al) hydrolysis were examined both theoretically and experimentally by constructing a solubility diagram for amorphous aluminum hydroxide (Al(OH)3(am)) and a distribution diagram of hydrolyzed Al species. First, thermodynamic data of Al species at 4 degrees C were calculated from that at 25 degrees C. A well confirmed polymeric Al species, AlO4Al12(OH)24(7+)(Al13), was involved in building the diagrams and, correspondingly, the non-linear simultaneous equations with 13 degrees were resolved. Secondly, polarized Zeeman atomic absorption spectrophotometry (AAS), 27Al nuclear magnetic resonance (NMR) spectroscopy, and ferron-based spectrophotometry were applied for constructing the practical diagrams. The results show that a decrease of temperature from 25 to 4 degrees C caused the Al(OH)3(am) boundary on the solubility diagram to shift toward the alkaline side by about 1.0 pH unit and the minimum solubility of Al(OH)3(am) to reduce by 1.0 log unit. The distribution diagram indicates that the monomeric Al, Al13, and solid-phase Al(OH)3 were alternately the predominant species with the increase of pH value during Al hydrolysis. At 25 degrees C, Al13 was the dominant species in a pH range of 4.0 to 4.5, whereas at 4 degrees C, All3 was the leading species in a pH range spaced from 4.5 to 6.3. The predominant species changed from the monomeric Al to the solid-phase Al(OH)3 over the range of 1.8 pH units at 4 degrees C in comparison with the range of 0.5 pH unit at 25 degrees C.     

Decomposition kinetics of dimethyl methylphospate(chemical agent simulant) by supercritical water oxidation

Supercritical water oxidation （SCWO） has been drawing much attention due to effectively destroy a large variety of high-risk wastes resulting from munitions demilitarization and complex industrial chemical. An important design consideration in the development of supercritical water oxidation is the information of decomposition rate. In this paper, the decomposition rate of dimethyl methylphosphonate（DMMP）, which is similar to the nerve agent VX and GB（Sarin） in its structure, was investigated under SCWO conditions. The experiments were performed in an isothermal tubular reactor with a H2O2 as an oxidant. The reaction temperatures were ranged from 398 to 633℃ at a fixed pressure of 24 MPa. The conversion of DMMP was monitored by analyzing total organic carbon （TOC） on the liquid effluent samples. It is found that the oxidative decomposition of DMMP proceeded rapidly and a high TOC decomposition up to 99.99% was obtained within 11 s at 555℃. On the basis of data derived from experiments, a global kinetic equation for the decomposition of DMMP was developed. The model predictions agreed well with the experimental data.