Degradation of aquatic humic material by ultraviolet light

Natural humic water was treated with ultraviolet (UV) light and UV + hydrogen peroxide . The effects on the dissolved organic carbon content (DOC), the UV-absorbance at 254 nm (UV-abs.), the molecular size distribution, pH, and mutagenic activity were monitored, and the identity and concentrations of the most abundant gas chromatographable organic degradation products were determined. The DOC content and the UV-abs. of the water decreased substantially during treatment with. The decreases were dependent on the time of irradiation (UV dose) as well as on the H2O2 dose applied. The humus macromolecules were degraded to smaller fragments during irradiation. At higher UV doses, however, part of the dissolved organic matter (DOM) was found to precipitate, probably as a result of polymerization. Oxalic acid, acetic acid, malonic acid, and n-butanoic acid were the most abundant degradation products detected. These acids were found to account for up to 20% and 80% of the DOM in UV- and waters, respectively. No mutagenic activity was generated by the UV irradiation or the treatment. It is further concluded that the substantial mutagenic activity formed during chlorination of humic waters cannot be decreased by using UV irradiation as a pretreatment step.

利福霉素生产菌产生钝化RifSV物质的分离及性质研究

利福霉素ＳＶ（简称ＲｉｆＳＶ）生产菌──地中海拟无枝菌酸菌在生物合成ＲｉｆＳＶ过程中，产生一种能钝化自身产物（ＲｉｆＳＶ）的物质．实验证实，该物质是由谷氨酸、天冬氨酸、赖氨酸及缬氨酸等１４种常见氨基酸组成的蛋白质．分子量（ＭＷ）约２．５×１０４Ｄ，等电点（ＰＩ）为５．７—６．１．在１００℃下加热１０ｍｉｎ，其活性丧失．作用于ＲｉｆＳＶ的最适ｐＨ值范围为７．４—８．６，最适温度为２９℃，初步证实该物质是一种酶（暂称利福霉素钝化酶）

纳米TiO_2催化下表层土壤中BaP的紫外光降解

采用光解试验,研究了紫外照射与纳米TiO2联合作用下,土壤表层中苯并[a]芘(BaP)的降解动力学;同时考察了催化剂的浓度、土壤pH、腐植酸和光质对BaP的光催化降解的影响。结果表明,土壤中BaP的光催化降解表现为准一级动力学。催化剂TiO2可以明显地促进土壤中BaP的光降解,较少量的催化剂(0.5%)使光解的半衰期从363.22h减少到103.26h。H+和OH-离子对BaP的催化光解起促进作用,在酸性和碱性土壤中BaP光催化降解高于中性土壤,酸性土壤中的降解速率最快。腐殖质吸收紫外光照射时,产生的活性氧中间产物能够攻击BaP,添加腐植酸能增加土壤表层中BaP的光催化降解。BaP的光解半衰期从无外加腐植酸的89.34h,减少到添加浓度分别为5、10、20和40mg·kg-1的29.37、32.69、35.73和38.51h。BaP的催化降解随波长的增加而降低,在波长254、310和365nm下,BaP降解的一级动力学常数分别为0.0078h-1、0.0061h-1和0.005h-1。

长期定位施肥对黑垆土剖面养分分布特征的影响

对黄土高原旱地 1 5年连续施肥后土壤剖面养分分布的研究发现 ,施化肥对土壤剖面有机质、全N、全P含量的影响深达 1 0 0cm以下 ,所有施肥处理有机质、全N、全P、NO3- N、有效P含量在耕层 (0～ 2 0cm)都有不同程度增加 ;40～ 60、60～ 80cm土层有机质、全N、全P都低于长年不施肥处理 ,造成土壤下层养分的亏缺。长期大量施用氮肥造成N素养分下淋累积 ;长期大量施用磷肥土壤耕层有效P显著提高 ,而 2 0cm以下土层变化不大。

植物对土壤紧实度的反应

概述了土壤紧实度对植物生长、水肥吸收、产量和水分利用效率的影响以及植物对紧实度反应机制的研究现状。

下辽河平原不同水肥条件对玉米养分吸收与分配的影响

利用持续16年的长期田间试验与气象观测资料,研究了下辽河平原不同施肥与降水条件对玉米体内养分浓度、养分在籽实与秸秆中的分配比以及每形成单位籽实产量所收获养分量等的影响。结果表明,玉米体内养分浓度及养分在籽实与秸秆中的分配比例明显受施肥、降水及作物生长状况的影响。在平水年条件下,养分在籽实内累积的比例最高,其中N、P、K分别较偏旱或偏涝年景平均相对提高26．2％、33．3％和21．3％。同时,作物生长状况愈好,形成单位籽实产量所需养分量有减少的趋势,这些都说明良好的水肥条件有利作物生长,也有利于提高作物体内养分的转化利用效率。

基于遥感-过程耦合模型的1988～2004年青海三江源区净初级生产力模拟

三江源区不仅是地处青藏高原的全球气候变化的敏感区,也是我国甚至亚洲最重要河流的上游关键源区。作为提供物质基础的植被净初级生产力(Netprimaryproduction,NPP),是评价生态系统状况的重要指标。该文应用已在碳通量观测塔验证,扩展到区域水平的遥感-过程耦合模型GLOPEM-CEVSA,以空间插值的气象数据和1km分辨率的AVHRR遥感反演的FPAR数据为模型主要输入,模拟并分析了1988～2004年该区NPP时空格局及其控制机制。结果表明,该区植被平均NPP为143.17gC·m–2·a–1,呈自东南向西北逐渐降低的空间格局,其中,以森林NPP最高(267.90gC·m–2·a–1),其次为农田(222.94gC·m–2·a–1)、草地(160.90gC·m–2·a–1)和湿地(161.36gC·m–2·a–1),荒漠最低(36.13gC·m–2·a–1)。其年际变化趋势在空间上呈现出明显的差异,西部地区NPP表现为增加趋势,每10a增加7.8～28.8gC·m–2;而中、东部表现为降低趋势,每10a降低13.1～42.8gC·m–2。根据显著性检验,NPP呈增加趋势(趋势斜率b>0),显著性水平高于99%和95%的区域占研究区总面积的13.43%和20.34%,主要分布在西部地区;NPP呈降低趋势(趋势斜率b<0),显著性水平高于99%和95%的区域占研究区面积的0.75%和3.77%,主要分布在中、东部地区,尤以该区长江和黄河等沿线区分布更为集中,变化显著性也更高。三江源NPP的年际变化趋势的气候驱动力分析表明,整个区域水平上该地区植被生产力受气候变化的主导,西部地区暖湿化趋势,造成了该地区生产力较为明显的、大范围的增加趋势;但东、中部地区则主要受人类活动的影响,特别是长江、黄河等河流沿线,是人类居住活动密集的地区,造成这些地区放牧压力较大、草地退化严重,而该地区暖干化趋势加剧了这一过程。

BaYF_5:Ce~(3+)纳米粒子的制备与光谱性质

在水/十六烷基三甲基溴化铵(CTAB)/正丁醇/正辛烷微乳液体系中成功的合成了BaYF5:Ce3+纳米粒子。运用X射线衍射(XRD)、环境扫描电子显微镜(ESEM)和荧光光谱等测试技术对所制备产物进行了表征。

LaGaO3 : A (A=Sm3+ and/or Tb3+) as promising phosphors for field emission displays

LaGaO3:Sm3+, LaGaO3:Tb3+ and LaGaO3: Sm3+, Tb3+ phosphors were prepared through a Pechini-type sol-gel process. X-Ray diffraction, field emission scanning electron microscopy, photoluminescence (PL), and cathodoluminescence (CL) spectroscopy were utilized to characterize the synthesized phosphors. Under excitation with ultraviolet light (250-254 nm), the LaGaO3: Sm3+, LaGaO3: Tb3+ and LaGaO3: Sm3+, Tb3+ phosphors mainly show the characteristic broadband emission (from 300 to 600 nm with a maximum around 430 nm) of the LaGaO3 host lattice, accompanied by the weak emission of Sm3+ ((4)G(5/2) -> H-6(5/2), H-6(7/2), H-6(9/2) transitions) and/or Tb3+ (D-5(3,4) -> F-7(6,5,4,3) transitions). However, under excitation by low-voltage electron beams (1-3 kV), the LaGaO3: Sm3+, LaGaO3: Tb3+ and LaGaO3: Sm3+, Tb3+ phosphors exhibit exclusively the characteristic emissions of Sm3+ and/or Tb3+ with yellow (Sm3+), blue (Tb3+, with low concentrations) and white (Sm3+ + Tb3+) colors, respectively.

Synthesis, characterization and mechanism of cetyltrimethylammonium bromide bilayer-encapsulated gold nanosheets and nanocrystals

Single-crystal Au nanosheets and fcc gold nanocrystals of uniform size were synthesized by a novel and simple route. The results of field-emission scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray diffraction (XRD) indicated the formation of the single-crystal structure of gold nanosheets and fcc nanocrystals. Energy-dispersive analysis of X-ray (EDAX) showed absorbance of cetyltrimethylammonium bromide (CTAB) molecules onto the surface of gold nanostructures.

The direct electrochemistry behavior of Cyt c on the modified glassy carbon electrode by SBA-15 with a high-redox potential

It is discovered that SBA-15 (santa barbara amorphous) can provide the favorable microenvironments and optimal direct electron-transfer tunnels (DETT) of immobilizing cytochrome c (Cyt c) by the preferred orientation on it. A high-redox potential (254 mV vs. Ag/AgCl) was obtained on glassy carbon (GC) electrode modified by immobilizing Cyt c on rod-like SBA-15. With ultraviolet-visible (UV-vis), circular dichroism (CD), FTIR and cyclic voltammetry, it was demonstrated that immobilization made Cyt c exhibits stable and ideal electrochemical characteristics while the biological activity of immobilized Cyt c is retained as usual.

Aggregation-based growth of silver nanowires at room temperature

We describe an aggregation-based growth mechanism for formation of silver nanowires at room temperature. It is found that the pH of solution and the concentration of L-cysteine capping molecules have an important effect on the formation and growth of nanowires. Characterization by atomic force microscopy (AFM) and UV-vis spectroscopy recorded as time clearly shows that the silver nanowires are grown at the expense of nanoparticles.