沈阳城市森林三维绿量的垂直分布

采用抽样调查法对沈阳城市森林5种功能类型的201块有效样地进行了调查,测算了样地内树木的三维绿量,利用将树木绿量汇集于树冠中心点的方法,对沈阳城市森林三维绿量垂直分布进行了研究。结果表明:沈阳城市森林的三维绿量垂直分布呈现典型的正态分布,其变化趋势与三维绿量垂直跨度分布相一致;新栽植树木对三维绿量垂直分布影响较小,三维绿量值更多地取决于三维绿量垂直跨度,即大龄级大树冠树木对三维绿量的贡献值最大。沈阳城市森林三维绿量垂直分布峰值为9 m。风景游憩林、附属林、道路林、生态公益林及生产经营林三维绿量垂直跨越层次依次为4.6、4.0、3.6、3.4、1.8,平均为3.9。风景游憩林和附属林三维绿量跨越层次较为丰富,灌木所占比例较大;生态公益林和道路林层次较为简单,灌木所占比例较小;生产经营林最为简单,三维绿量垂直跨越层次多为1层,三维绿量垂直分布峰值为5 m。

水稻和稗草共生土壤微生物生物量碳及酶活性的变化

以稻田稗草、化感水稻PI312777和普通水稻辽粳9为试材,研究了田间稗草和水稻1∶1共生条件下,土壤微生物生物量碳及脱氢酶、脲酶和转化酶活性的变化.结果表明:在稗草的干扰下,化感水稻PI312777根区土壤微生物生物量碳含量比单作减少了50.52%(P<0.01),而行间土壤微生物生物量碳含量增加;普通水稻辽粳9根区土壤微生物生物量碳含量比单作减少了38.99%(P<0.01),但其行间土壤微生物生物量碳含量无明显变化.两个水稻品种根区土壤脱氢酶活性均被显著抑制(P<0.05),下降率都在20%以上;PI312777根区土壤脲酶和转化酶活性均被显著促进(P<0.01);而辽粳9根区土壤转化酶活性也被显著抑制(P<0.01),但脲酶活性无明显变化.化感水稻根区土壤微生物生物量碳含量的显著减少及脲酶、转化酶活性的增加是其化感特性的表现,表明土壤微生物和酶均参与了水稻和稗草的种间作用,化感水稻具有抗稗草干扰的明显优势.

银杏种子生长特性及其生理变化的研究

从纵径、横径、体积、重量等方面分析了银杏种子的生长特性及其生长过程中水分、糖类物质、脂肪酸、氨基酸的生理变化 .结果表明 ,银杏种子的生长过程曲线为典型的单“S”型 ,种子纵径、横径、体积、重量、绝对含水量随生长过程呈“S”形变化 .各种生理物质含量随种子生长过程呈规律性变化 ,且各有其特点 .其中在种子生长后期糖类物质总量表现出上升的趋势 ,表明它们是种子中主要的营养储存物质 .成熟种子含淀粉 8.4%、葡萄糖 6.7%、果糖 4.2 %、多糖 0 .0 2 %、二糖 0 .0 1% ;含肉豆蔻酸 10 .6%、棕榈烯酸 4.1%、亚麻酸 2 .4%、硬脂酸1.9%、油酸 1.1%、亚油酸 0 .4% .银杏种子富含 15种氨基酸 ,成熟种子中总含量为 1.5 6g·10 0 g-1FW ,其中以赖氨酸、天门冬氨酸、丙氨酸、精氨酸、组氨酸、谷氨酸、异亮氨酸的含量较高 ,它们的含量依次为 0 .2 87%、0 .163 %、0 .13 6%、0 .13 3 %、0 .12 3 %、0 .115 %、0 .0 95 % .

油松水源保护林人工诱导更新与定向恢复机理

以油松水源保护林为对象,进行人工诱导更新与定向恢复机理研究。结果表明,在郁闭林分内油松更新苗密度平均为5 375株.hm-2,更新苗年龄为1~2年,而在人工Gap“效应岛”样地内,更新苗密度平均为17 062.5株.hm-2,其中1~2年、3~4年、5~6年生更新苗分别占73.44%,13.97%和12.59%;生长季光照强度在0、1.5和2.0 m三个不同高度梯度上,在Gap内部的平均值分别为289.0×100、542.0×100和589.0×100 lux,在对照林分内分别为139.0×100、146.0×100和246.0×100lux;从夏季观测到的空气温度平均值日变化分析,在白天Gap内的温度高于郁闭林分内部,温差可差2~3℃,在夜间Gap内的温度低于郁闭林分内,温差可差0.5~1℃;在白天6:00~11:00,人工Gap“效应岛”内空气湿度明显低于郁闭林分内,在其它时间段大致相当;对于同一层次土壤而言,Gap内的土壤温度明显高于郁闭林分内且变化幅度大,在0、10和20 cm三个梯度上Gap与郁闭林分相比土壤温度最大差值分别可达10、5和2℃;0~10、10~20和20~30 cm三个层次平均土壤含水量在Gap内分别为16.9%1、5.1%和12.3%,在郁闭林分内分别为14.6%、12.5%和9.9%。总体上比较二者的光照强度、空气温度、空气湿度、土壤温度、土壤水分等有显著差异,因此人工Gap“效应岛”的创建是诱导其内部微环境因子变化的基础,也是油松水源保护林定向恢复更新的机理之所在。

中国东北西部地区荒漠化发展前沿区域的遥感研究

依据 1 996年 7～ 9月和 1 988年 8～ 1 0月两个时期的LandsatTM遥感信息 ,分别对中国东北西部地区荒漠化发展前沿的典型区域吉林省乾安县的盐渍化、吉林省梨树县土地沙化变化和乌尔吉木伦河与新开河间的土地利用状况 ,进行遥感解译和实地调查。分析研究结果表明 ,东北西部这三个区域的生态环境 1 996年比 1 988年有所恶化 ,主要表征为盐渍化和沙化土地向东有较强发展和蔓延 ,撂荒地显著扩大 ,与沙化土地面积量级接近。由此东北西部应该成为我国荒漠化和生态环境治理的重点区域

Synthesis and characterization of novel biodegradable poly(carbonate ester)s with photolabile protecting groups

Novel biodegradable poly(carbonate ester)s with photolabile protecting groups were synthesized by ring-opening copolymerization Of L-lactide (LA) with 5-methyl-5-(2-nitro-benzoxycarbonyl)-1,3-dioxan-2-one (MNC) with diethyl zinc (Et2Zn) as catalyst. The poly(L-lactide-co-5-methyl-5-carboxyl-1,3-dioxan-2-one) (P(LA-co-MCC)) was obtained by UV irradiation Of poly(L-lactide acid-co-5-methyl-5-(2-nitro-benzoxycarbonyl)-1,3-dioxan-2-one) (P(LA-co-MNC)) to remove the protective 2-nitrobenzyl group.

Assembly of supramolecular compounds with water-soluble calix[4]arenes

Three new copper compounds, Cu-2[C12H8N2](2)[C28H2OS4O16][H2O](11.9) (1), Cu-2[C12H8N2](3)[C28H20S4O16][H2O](5) (2), and Cu-2[C12H8N2](4)[C24H12S8O16][H2O](10.5) (3), were hydrothermally synthesized and structurally determined by X-ray diffraction and TG-DTA analyses. Interestingly, Compounds 1 and 2 were synthesized in a one-pot reaction. Complexes 1 and 3 contain capsule units, which are further assembled into three-dimensional (3-D) architectures with a-Po-related topology by pi-pi stacking and/or hydrogen-bonding interactions.

Hydrogenation of cinnamaldehyde over Pt/RHCs in supercritical carbon dioxide - Influence of support pretreatment and phase behavior

The selective hydrogenation of cinnamaldehyde (CAL) was investigated using rice husk-based porous carbon (RHCs) supported platinum catalysts in supercritical carbon dioxide (SCCO2). The effects of surface chemistry treatment of the support and the reaction phase behavior have been examined. The Pt/H-RHCs (HNO3-pretreated) was more active for CAL hydrogenation compared with Pt/NH3 - RHCs (NH3 center dot H2O-pretreated). The Pt/RHCs catalyst exhibited a higher selectivity to cinnamyl alcohol (COL) compared with commercial catalyst of Pt/C, which is relative to the micro - mesoporosity structure of the RHCs.

Novel spiro-fluorenes from tandem radical addition for liquid crystalline monodisperse conjugated oligomers

3'-Nonafluorobutylmethyl-4'-methyl-spiro[cyclopentyl-9,1']fluorenes were successfully synthesized via tandem radical-addition reactions between 9,9-diallylfluorenes and perfluorobutyl iodide in the presence of a radical initiator followed by reduction under mild conditions. Single crystal analysis indicates that two substituents at 3,4-positions of cyclopentane are in a maleinoid form. Accordingly, four oligo(fluorene-co-bithiophene)s with the same molecular length of similar to 10 nm (7 fluorene units and 12 thiophene units) containing one to three novel spiro-fluorene units were synthesized.

Five supramolecular compounds of water-soluble sulfonylcalix[4]arenetetrasulfonate showing two calixarene conformations

Five new compounds of sulfonylcalix[4]arenetetrasulfonate (SC4AS), [H7Na(H2O)(3)(SC4AS)(phen)(5)](H2O)(11.9) (1), [H6Mn(H2O)(4)(SC4AS)(phen)(5)] (H2O)(12.7) (2), [Cu-4(SC4AS) (phen)(6)] (H2O)(4.5) (3), {[Cu (2)(SC4AS) (bpy)(2)][Cu(bpy)(2)(H2O)](2)} (H2O)(6.6) (4), and {[Zn-2(SC4AS) (phen)(2)][Zn(phen)(2)(H2O)(2)](2)} (H2O)(7) (5) (where phen 1,10-phenanthroline and bpy = 2,2'-bipyridine), were synthesized by a hydrothermal method and structurally determined by single crystal X-ray diffraction. The SC4AS ligand adopts partial cone conformation in compounds 1 and 2 and 1,2-alternate form in compounds 3-5. According to the structural analysis and density functional theory (DFT) calculations, we suggest that the metal can affect the conformation of SC4AS.

General and Facile Method To Prepare Uniform Y2O3:Eu Hollow Microspheres

Well-shaped Y2O3:Eu hollow microspheres have been successfully prepared on a large scale via a urea-based homogeneous precipitation technique in the presence of colloidal carbon spheres as hard templates followed by a subsequent heat treatment process. XRD results demonstrate that all the diffraction peaks of the samples can be well indexed to the pure cubic phase Of Y2O3. TEM and SEM images indicate that the shell of the uniform hollow spheres, whose diameters are about 250 nm, is composed of many uniform nanoparticles with diameters of about 20 nm, basically consistent with the estimation of XRD results. Furthermore, the main process in this method was carried out in aqueous condition, without the use of organic solvents or etching agents. The as-prepared hollow Y2O3:Eu microspheres show a strong red emission corresponding to the D-5(0)-F-7(2) transition of the Eu3+ ions under ultraviolet or low voltage excitation, which might find potential applications in fields such as light phosphor powders, advanced flat panel displays, field emission display devices, and biological labeling.

Rectangular Silver Nanorods: Controlled Preparation, Liquid-Liquid Interface Assembly, and Application in Surface-Enhanced Raman Scattering

In this paper, we for the first time report a polyol method for large-scale synthesis of rectangular silver nanorods in the presence of directing agent and seeds. This method has some clear advantages including simplicity, high quality, and ease of scaleup. Silver nanowires or silver nanorods with a submicrometer diameter could also be facilely prepared when the reaction parameters are slightly changed. Furthermore, a liquid-liquid assembly strategy has been employed to construct uniform rectangular silver nanorod arrays on a solid substrate which could be used as surface-enhanced Raman scattering (SERS) substrates with high SERS activity, stability, and reproducibility. It is found that the SERS spectra obtained from the probe molecules with the different concentrations show different SERS intensifies. As the concentration of 4-aminothiophenol (4-ATP) or rhodamine 6G (R6G) increases, the SERS intensities progressively increase. The enhancement factor for 4-ATP and R6G should be as large as 5.06 x 10(4) or much larger than the value of 5.06 x 10(8), respectively.

Tris(2,2 '-bipyridyl)ruthenium(II) electrochemiluminescent detection of coreactants containing aromatic diol group by the interaction between diol and borate anion

Previous studies show that aromatic diols inhibited Ru(bpy)(3)(2+) electrochemiluminescence (ECL), and all reported Ru(bpy)(3)(2+) ECL methods for the determination of aromatic diols-containing coreactants are based on inhibition of Ru(bpy)(3)(2+)/tripropylamine ECL. In this study, the interaction between diol and borate anion was exploited for Ru(bpy)(3)(2+) ECL detection of coreactants containing aromatic diol group using epinephrine as a model analyte. The interaction prevented from the inhibition of Ru(bpy)(3)(2+) ECL by aromatic diol group of epinephrine. As a result, epinephrine was successfully detected in the absence of tripropylamine simply by using borate buffer solution as the supporting electrolyte. Under the optimum conditions, the log of the ECL intensity increases linearly with the log of epinephrine concentrations over the concentration range of 1.0x10(-9)-1.0x10(-4) M. The detection limit is 5.0x10(-10) M at a signal-to-noise ratio of three. The proposed method exhibit wider dynamic range and better detection limit than that by inhibited Ru(bpy)(3)(2+) ECL method. The relative standard deviation for 14 consecutive determinations of 5 mu M epinephrine was 3.5%. The strategy by interaction with borate anion or boronate derivatives is promising for the determination of coreactants containing aromatic diol group or aromatic hydroxyl acid group. Such interaction can also be used to avoid interference from aromatic diols or aromatic hydroxyl acids.