云南稻核心种质F2主要形态性状变异及地理生态研究

种质资源是水稻育种的重要基因来源.掌握育种材料遗传背景信息,可为发掘优异种质,选育优良性状新品种提供依据.以548份云南稻核心种和云南主栽籼稻品利慎屯502(Oryza satica)、粳稻品种合系35(Oryzasatica)配制的杂种F2(498份)为材料,采用群体遗传学的方法,研究云南稻核心种质杂种F2代的11个形态性状的综合变异系数、遗传多样性指数(Shannon指数)及其地理分布.结果表明:(1)F2存在明显的性状分化和遗传变异,以有效穗、穗颈长、穗下节长、每穗实粒数、秕粒数、总粒数和结实率的综合变异系数高,遗传多样性丰富;(2)滇西南(临沧、思茅、德宏、西双版纳)和滇东南(文山、红河)的材料在表型性状上存在更大的分化,综合变异系数高,遗传多样性丰富;保山、昭通、曲靖次之;怒江、丽江、迪庆、大理最低.     

温度对小叶海金沙生长的影响

用野外调查测定和室内模拟的方法研究了温度对小叶海金沙生长的影响.结果表明,小叶海金沙疯狂生长群落中的温度比正常生长群落高,且温度与其净光合速率呈极显著正相关,而这两种类型群落内大气相对湿度以及光照差异较小.此外,土壤养分和土壤pH与小叶海金沙的生长速度无明显的关联性.根据研究结果推测:温度可能是小叶海金沙疯狂生长原因之一.     

Biogenic palladium prepared by activated sludge microbes for the hexavalent chromium catalytic reduction: Impact of relative biomass

• Pd nanoparticles could be reduced and supported by activated sludge microbes. • The effect of biomass on Pd adsorption by microbes is greater than Pd reduction. • More biomass reduces Pd particle size, which is more dispersed on the cell surface. • When the biomass/Pd add to 6, the catalytic reduction rate of Cr(VI) reaches stable. Palladium, a kind of platinum group metal, owns catalytic capacity for a variety of hydrogenations. In this study, Pd nanoparticles (PdNPs) were generated through enzymatic recovery by microbes of activated sludge at various biomass/Pd, and further used for the Cr(VI) reduction. The results show that biomass had a strong adsorption capacity for Pd(II), which was 17.25 mg Pd/g sludge. The XRD and TEM-EDX results confirmed the existence of PdNPs associated with microbes (bio-Pd). The increase of biomass had little effect on the reduction rate of Pd(II), but it could cause decreasing particle size and shifting location of Pd(0) with the better dispersion degree on the cell surface. In the Cr(VI) reduction experiments, Cr(VI) was first adsorbed on bio-Pd with hydrogen and then reduced using active hydrogen as electron donor. Biomass improved the catalytic activity of PdNPs. When the biomass/Pd (w/w) ratio increased to six or higher, Cr(VI) reduction achieved maximum rate that 50 mg/L of Cr(VI) could be rapidly reduced in one minute.     

典型羟基化多溴联苯醚(OH-PBDEs)小鼠肝微粒体的体外代谢及关键代谢CYP450酶系的研究

羟基化多溴联苯醚(OH-PBDEs)是一类具有内分泌干扰效应的酚类化合物,本研究以小鼠肝脏微粒体作为研究对象,考察了4种典型OH-PBDEs(3-OH-BDE-47、5-OH-BDE-47、6-OH-BDE-47和2′-OH-BDE-68)的体外代谢.研究结果表明,4种OH-PBDEs在小鼠肝脏微粒体中均能被代谢;OH-PBDE结构上的醚键(O)、羟基(OH)和溴原子(Br)的相对位置会影响其代谢效率,OH位于苯环上醚键邻位更有利于其代谢,即6-OH-BDE-47表现出相对较高的代谢率;抑制剂实验发现CYP1A2和CYP3A4是4种典型OH-PBDEs主要的CYP450代谢亚型.     

宝鸡高新区春节前后大气中黑碳浓度特征及来源解析

基于春节前后(2018年1月1日—2018年3月31日)宝鸡市高新区宝鸡文理学院站点的黑碳气溶胶(BC)、浊度仪、颗粒态污染物(PM_(10)、PM_(2.5)和PM_(1.0))、气态污染物(CO、NO_2、SO_2和O_3)的逐时数据及常规气象数据,对宝鸡市高新区BC气溶胶的时间变化特征、来源及影响因素进行分析.结果表明,观测期间BC质量浓度的变化范围为0.01—5.62μg·m~(-3),平均浓度为0.63μg·m~(-3).BC与风速和能见度均呈负相关.观测期间BC浓度日变化呈"双峰双谷"型,峰值出现在09:00和19:00,谷值出现在05:00和16:00;寒假前BC浓度昼夜变化整体高于寒假期间和春季开学,可能与寒假前频繁的人为活动,不易扩散的气象条件有关.BC占PM_(2.5)的0.84%,其吸收作用占大气消光的2.14%.除O_3外,BC日平均浓度与PM_(2.5)、CO和NO_2呈显著相关,相关系数分别为0.626、0.623和0.473,说明BC气溶胶与之均有部分共同源.     

干旱区绿洲土壤中重金属的形态分布及生物有效性研究

测定了Cd、Pb、Zn和Ni等重金属在不同处理土壤中的全量和各赋存形态,以及它们在盆栽试验油菜（Brassica cole）中的质量分数,并利用Pearson相关系数分析了该区土壤-油菜体系的生物有效性。结果表明,供试绿洲土壤原状土中,Cd、Pb、Zn和Ni均以稳定的残渣态形式存在;而在处理土壤中,重金属被钝化的量有限,Cd的存在形式主要以碳酸盐态为主,Pb、Zn和Ni则主要以铁锰氧化态为主。根据相关性分析,油菜根部和叶部的Ni质量分数均与土壤中Ni的各非残渣态分布系数有相关性,表明当土壤中Ni以非残渣态存在时,活动性Ni的质量分数较高,其被生物吸收利用的可能性也较大;油菜根部的Zn质量分数与土壤中Zn的碳酸盐结合态分布系数显著的正相关性;油菜各部位Cd和Pb的质量分数与土壤中Cd和Pb的各形态分布系数之间无显著相关关系。     

加压溶氧光催化反应器降解活性艳红X-3B

探讨了加压溶氧条件对活性艳红X-3B的降解与脱色的作用,考察了加压条件下pH值,TiO2投加量及温度等对活性艳红X-3B降解的影响.结果表明,加压条件与常压条件下变化趋势基本一致.加压充氧有助于活性艳红X-3B的降解与脱色,加压充N2对反应基本没有作用,说明增加活度不是关键因素,加压使溶液中溶解氧增加是导致活性艳红X-3B降解与脱色的主要原因.光催化降解过程,发色基团最易被打碎,60min内降解效果显著,而萘环和苯环降解效果不十分明显.CODCr的降解与色度的褪除成正相关,脱色率越高,COD的降解率也越高.     

Urea formation from carbon dioxide and ammonia at atmospheric pressure

Urea synthesis, currently the largest use of carbon dioxide in organic synthesis, is conventionally operated at high pressure and high temperature. Here, we report for the first time that urea forms at atmosphere and ambient temperatures by negative corona discharge in gas phase. The conversion of CO₂ and yields of a solid mixture of urea and ammonium carbamate, which was identified by the ¹³C NMR spectrum, rise with reducing temperatures and increasing molar ratios of NH₃/CO₂ and discharge frequencies. The conversion of carbon dioxide was found to be 82.16?% at 20?°C and 1?atm with a molar flow ratio of n(NH₃)/n(CO₂) of 2.5. High pressure and high temperature as energy inputs are not necessary.     

Reduction of hexavalent chromium with scrap iron in a fixed bed reactor

The reduction of hexavalent chromium by scrap iron was investigated in continuous long-term fixed bed system. The effects of pH, empty bed contact time (EBCT), and initial Cr(VI) concentration on Cr(VI) reduction were studied. The results showed that the pH, EBCT, and initial Cr(VI) concentration significantly affected the reduction capacity of scrap iron. The reduction capacity of scrap iron were 4.56, 1.51, and 0.57 mg Cr(VI)·g^-1 Fe⁰ at pH 3, 5, and 7 (initial Cr(VI) concentration 4 mg·L^-1, EBCT 2 min, and temperature 25°C), 0.51, 1.51, and 2.85 mg Cr(VI)·g^-1 Fe⁰ at EBCTs of 0.5, 2.0, and 6.0 min (initial Cr(VI) concentration 4 mg·L^-1, pH 5, and temperature 25°C), and 2.99, 1.51, and 1.01 mg Cr(VI)·g^-1 Fe⁰ at influent concentrations of 1, 4, and 8 mg·L^-1 (EBCT 2 min, pH 5, and temperature 25°C), respectively. Fe(total) concentration in the column effluent continuously decreased in time, due to a decrease in time of the iron corrosion rate. The fixed bed reactor can be readily used for the treatment of drinking water containing low amounts of Cr(VI) ions, although the hardness and humic acid in water may shorten the lifetime of the reactor, the reduction capacity of scrap iron still achieved 1.98 mg Cr⁶⁺·g^-1 Fe. Scanning electron microscope equipped with energy dispersion spectrometer and X-ray diffraction were conducted to examine the surface species of the scrap iron before and after its use. In addition to iron oxides and hydroxide species, iron-chromium complex was also observed on the reacted scrap iron.     

Characterization of soil low-molecular-weight organic acids in the Karst rocky desertification region of Guizhou Province, China

Soil low-molecular-weight (LMW) organic acids play important roles in the soil-forming process and the cycling of nutrients in Karst regions. In this study, we quantified the contents of LMW organic acids (including lactate, acetate, formate, malate, and oxalate) in soil solution over the Karst region of Guizhou Province, China using ion chromatography. The concentration of total LMW organic acids in topsoil solution ranged from 0.358 to 1.823 μmol·g^-1, with an average of 0.912 μmol·g^-1. The mean concentrations of lactate, acetate, formate, malate, and oxalate were 0.212±0.089, 0.302±0.228, 0.301±0.214, 0.014±0.018 and 0.086±0.118 μmol·g^-1, respectively. There were also significant difference in the contents of these acids among four phases of rocky desertification, and their concentrations decreased with the aggravation of rocky desertification. The concentrations of the LMW organic acids were significantly positive correlated each other. Significant positive correlations were also observed among individual LMW organic acids in soil solution, and between them and soil available P, available K, exchangeable Ca, respectively. Furthermore, the concentrations of LMW organic acids were significantly positively correlated with inorganic anions (chlorides, nitrates, and sulfates) in Karst topsoil solution. Therefore, the concentrations of soil LMW organic acids might be one of driving force in the Karst rock desertification process in Guizhou Province.