非生长季长白山红松针阔叶混交林CO_2通量特征

采用开路式涡度相关系统对长白山红松针阔叶混交林非生长季的CO2通量特征进行连续监测。结果显示:非生长季CO2通量变动范围为-0·3~0·5mg·m-2s-1;秋末与初春均为显著的释放过程,虽然气温低于生物学最低温度,但在晴朗的午间,森林仍有数小时表现为碳汇的特征;在冬季覆雪状态下,森林存在微弱的相对恒定的CO2释放,在融雪阶段有一释放高峰;土壤温度高于0℃时,净生态系统碳交换量与5cm深土壤温度呈指数相关变化。观测期间(190d),长白山红松针阔叶混交林净碳交换量为127g C·m-2,整体表现为一定强度的碳释放。

高浓度CO_2下红松幼苗根系呼吸对土壤呼吸的贡献(英文)

本文于2003年5月至10月在长白山森林生态系统定位站内研究了高浓度CO2(500和700靘olmol-1)对红松幼苗土壤呼吸以及根系呼吸对土壤呼吸的贡献。经过4个生长季高浓度CO2的处理,利用LI-6400-09土壤呼吸室对红松幼苗土壤总呼吸和根系呼吸进行了测定。为了区分根系呼吸对土壤总呼吸的贡献,本文采用了PVC管断根法,即每种处理下将三根PVC管插入土壤中30cm以切断根系,从而终止了植物冠层对根系碳水化合物的供应。分别于6月16日、8月20日和10月8日对管内外土壤呼吸进行了测定。结果表明大气和土壤5cm温度都存在明显的日变化,但不同处理之间没有显著差别(P>0.05)。土壤总呼吸和断根土壤呼吸也有明显的日变化和季节变化。不同处理之间土壤总呼吸和断根土壤呼吸差异显著(P<0.01)。6月16日、8月20日和10月8日不同处理下土壤总呼吸和根系呼吸的贡献的平均值分别为3.26、4.78和1.47靘olm-2s-1以及11.5%、43.1%和27.9%。图5表1参38。

两种五倍子蚜虫冬寄主藓类植物的光合特性及其与光照、温度和植物体水分含量变化的关系

使用CI 30 1PS (CIDInc .USA )对生长于冬季和春季的大羽藓 (Thuidiumcymbifolium )与垂藓(Chrysocladiumretrorsum )的净光合速率 (Pn)及其与光照、温度和植物体水分含量的关系进行了研究 .结果表明 ,大羽藓和垂藓的光合能力分别达到 14 1和 117μmolCO2 kg-1·dw·s-1,光合能力从冬季到春季呈上升趋势 .这两种藓类植物的光响应曲线比较相似 ,光饱和点高达 80 0～ 90 0 μmol·m-2 s-1,光补偿点为 40～ 5 0 μmol·m-2s-1,光合作用最适温度在春季为 2 5～ 36℃ ,而冬季为 2 0～ 30℃ .同时对于低温又具有很强的抗性 ,在冰点以下的温度条件下 (-15～ 0℃ )能够保持一定的净光合 .净光合速率的水分响应曲线表明 ,这两种藓类的最适水分含量为 2 0 0～ 30 0 (4 0 0 ) %dw ,水分含量降低到 15 0 %dw时光合作用开始受到抑制 ,在 40 %～ 5 0 %dw时净光合降低到零或略变为负数 .结果表明 ,大羽藓和垂藓都属于耐干旱、强阳性的藓类 ,但垂藓在这几个方面略逊于大羽藓 .

南亚热带森林群落演替过程中林下土壤的呼吸特征

采用CI-310便携式光合作用系统及其附件,测定了广东省黑石顶自然保护区南亚热带森林演替系列中的马尾松林和松阔混交林林下土壤的呼吸速率。测定结果显示:在自然条件下,马尾松林土壤呼吸速率在1.650~4.0μmolCO2m-2s-1,松阔混交林土壤呼吸速率在1.70~3.950μmolCO2m-2s-1之间。林下土壤呼吸速率与温度和土壤空气相对湿度可用拟合,据此并结合当地气象资料推算出马尾松林和松阔混交林的年均土壤呼吸量分别为31.027、36.629 tCO2hm-2,后者高于前者。

鼎湖山常绿针阔叶混交林CO_2通量估算

鼎湖山通量站是中国通量网络(ChinaFLUX)中4个森林站之一,采用开路涡度相关方法,对南亚热带常绿针阔叶混交林进行生态系统尺度的CO2通量长期定位观测．利用2003,2004年2整年观测资料,分析该生态系统CO2通量时间变化特征及其受环境因子的制约关系．通过坐标转换、WPL订正和质量控制后,发现本通量站存在明显的夜间泄漏问题,因此采用Michaelis-Menten模型,利用白天(PAR>1．0μmol-1Photons·m-2·s-1)湍流充分条件-F(u*>0．2m·s-1)的通量资料,逐月拟合净

东北地区大豆鼓粒期光合特性的研究

用LI-6400光合测定系统对东北地区大豆鼓粒期叶片光合速率对光合有效辐射通量密度的响应特征和晴天光合速率、光能利用率、水分利用率等特性的日变化规律进行了研究。结果表明,光合速率对光合有效辐射通量密度的响应特征遵循Michaelis-Menten方程,在自然光条件下,上下两层叶片综合考虑,最大光合速率平均为37.25μmolm-2s-1,表观初始量子效率平均为0.0376。在晴天,光合速率、蒸腾速率、气孔导度以及光合有效辐射通量密度、环境温度随时间的变化可以用正弦函数模拟,但其峰值出现的时间不同,光合速率

Chiral ligand 2-(2 '-piperidinyl)pyridine: synthesis, resolution and application in asymmetric diethylzinc addition to aldehydes

Chiral ligand 2-(2'-piperidinyl)pyridine 1 has been synthesized in good overall yield by sequential benzylation, hydrogenation and debenzylation of 2,2'-bipyridine. Its enantiomerically pure enantiomers have been obtained by resolution of 2-(1-benzyl-2-piperidinyl)pyridine 2 with D-tartaric acid (or L-tartaric acid) followed by debenzylation. The absolute configuration was determined by X-ray analysis of the (S)-2 D-tartrate. It was demonstrated that I can be used as an effective enantioselective catalyst in the addition of diethylzinc to aldehydes.

Preparation of highly conductive, self-assembled gold/polyaniline nanocables and polyaniline nanotubes

One-dimensional gold/polyaniline (Au/PANI-CSA) coaxial nanocables with an average diameter of 5060 nm and lengths of more than 1 mu m were successfully synthesized by reacting aniline monomer with chlorauric acid (HAuCl4) through a self-assembly process in the presence Of D-camphor-10-sulfonic acid (CSA), which acts as both a dopant and surfactant. It was found that the formation probability and the size of the Au/PANI-CSA nanocables depends on the molar ratio of aniline to HAuCl4 and the concentration of CSA, respectively. A synergistic growth mechanism was proposed to interpret the formation of the Au/PANI-CSA nanocables. The directly measured conductivity of a single gold/polyaniline nanocable was found to be high (approximate to 77.2S cm(-1)). Hollow PANI-CSA nanotubes, with an average diameter of 50-60 nm, were also obtained successfully by dissolving the Au nanowire core of the Au/PANI-CSA nanocables.

Simultaneous determination of 2-aminothiazole, 2-aminobenzothiazole and 2-mercaptobenzothiazole by capillary electrophoresis with end-column amperometric detection

Capillary electrophoresis with amperometric detection is evaluated for the simultaneous determination of 2-aminothiazole (A), 2-amino-benzothiazole (AB), 2-mercaptobenzothiazole (AM). The cyclic voltammogram, hydrodynamic voltammogram, effect of pH, concentration of buffer and separation voltage on the separation and the detection were studied. The conditions were optimized as follows: 50 mM phosphate buffet; pH 6.0, 2s at 17.5 kV sample injection, separation at 17.5 kV, 1.2 V as detection potential. The method provided low detection limit as 0.5 mu M, 0.05 mu M and 0.01 mu M, wide linear range 2-200 mu M, 10-200 mu M and 0.025-100 mu M for A, AB, and AM, respectively. The variations in peak current and migration time for 15 consecutive injections of a standard containing 5 mu M each compound were 3.7, 2.1, and 3.9%, and 1.2, 0.8, and 1.2%, for A, AB and AM, respectively. This method was employed to analyze river water.

Asymmetric polymerization of the mixture of TrMA and MMA initiated by chiral complexes

A mixture of triphenylmethyl methacrylate (TrMA) and methyl methacrylate (MMA) was polymerized with chiral anionic initiator, such as fluorenyl lithium-(-)-sparteine [FlLi-(-)-Sp] and fluorenyl lithium-(+)-2S,3S-dimethoxy-1,4-bis(dimethylamino) butane [FlLi-(+)-DDB] in toluene at -78 degrees C. The results show that after the stable helix formed, when FlLi-(+)-DDB was used as the initiator, TrMA and MMA could be copolymerized, whereas when FlLi-(-)-Sp was used, the two monomers tended to be selectively polymerized into two polymers. This phenomenon has been explained by the existence of helix-selective polymerization. (C) 1997 John Wiley & Sons, Inc.

SYNTHESIS AND PROPELLER-PROPELLER TRANSITION OF OPTICALLY-ACTIVE POLY(DIPHENYL-O-TOLYLMETHYL METHACRYLATE)

Diphenyl-o-tolylmethyl methacrylate (DPTMA) was synthesized and polymerized using initiators of organolithium complexes with (+) - (2S,3S) -dimethoxy-1,4-bis(dimethylamino) butane (DDB) and (-) -sparteine (Sp) as the chiral ligands. DDB was suitable for its complex effective to prepare optically active poly(diphenyl-o-tolylmethyl methacrylate) (PDPTMA) with one-handed helical conformation, whereas only low-molecular weight polymer was formed when Sp was used as ligand due to the repulsive hindrance between the triarylmethyl group and the ligand. A new mutarotation, propeller-propeller transition, was observed for PDPTMA from the optical rotation curves and CD spectra in THF solution. The equivalent period of PDPTMA was estimated to be 14 angstrom based on the x-ray diffraction. (C) 1993 John Wiley & Sons, Inc.

STUDIES ON THE REACTIONS OF TRANSITION-METAL HYDRIDES WITH HETEROCUMULENES .6. REACTION OF CP2ZR(H)CL WITH RNCS (R=C6H5, 2-C10H7, C-C6H11 AND N-C4H9)

The novel NS-containing zirconacycle complexes Cp2ZrCl[SC(H)NR] (1a, R = C6H5; 1b, R = 2-C10H7; 1c, R= C-C6H11; 1d; R = n-C4H9) were obtained by insertion reactions of Cp2Zr(H)Cl with RNCS. 1(a-d) could react further with Cp2Zr(H)Cl to yield a sulphur-bridging compleX (Cp2ZrCl)2S (2) and a Schiff base RN=CH2. The crystal structure of la has been determined by X-ray analysis.

THE ELECTROCATALYTIC OXIDATION OF ASCORBIC-ACID ON PRUSSIAN BLUE FILM MODIFIED ELECTRODES

The kinetics of prussian blue (PB) film itself during the redox process and of the catalytic oxidation of ascorbic acid (AH_2) on it have been studied in detail. The charge transfer diffusion coefficient D_(ct) in PB film is determined as 2.62×10~(-10)cm~2·s~(-1), using potential-step chronoamperometry, chronocoulometry and constant-current chronopotentialmetry, respectively. The rate constant of the cross-exchange reaction between AH_2 in solution and the active centers in PB film is measured in rotating d...

STUDY ON MEASUREMENT OF DIFFUSION-COEFFICIENT OF LI ATOM IN LIQUID ALUMINUM

The tess potential-concentration curve was first applied to measure the concentration of an alloy. Attempt to use the V-c curve of Al-Li alloy in measuring the diffusion coeffictent of Li atom in liquid aluminium with anode chronopotentiometry at 720℃, was made and D_(Li/Al=4.94×10~(-5)cm~2·s~(-1) was obtained. The value is well consistent wish the theoretical value, D_(Li/Al)=4.85×10~(-5)cm~2·s~(-1) in terms of Stokes-Einstein equation.

抗坏血酸在普鲁士蓝薄膜修饰电极上的电催化氧化

本文详细研究了普鲁士蓝(PB)薄膜本身电荷传输过程的动力学及PB薄膜催化抗坏血酸(AH_2)电氧化的动力学,用电位阶跃计时电流法和计时电量法,恒电流计时电位法测得PB膜中电荷传输表观扩散系数D_(ct)平均为2.62×10~(-10)cm~2·s~(-1);用RDE法测得AH_2在PB薄膜上催化氧化的速率常数为1.23×10~8cm~3·mol~(-1)·s~(-1),催化反应对AH_2为一级,只发生在PB薄膜与溶液的界面上,整个催化过程受到溶液中的传质、膜内部的电荷传输及膜与溶液界面上交叉反应三种因素单独或联合控制,实际出现四种动力学情况。