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具有10微秒时间分辨率的叶绿素荧光诱导动力学测量及其在森林衰退研究中的应用。

Measurement of the chlorophyll fluorescence induction kinetics with a 10 microseconds time resolution and its application in the forest decline research.

作者信息

Ruth B

机构信息

GSF-Forschungszentrum für Umwelt und Gesundheit, Medis-Institut, Neuherberg, Federal Republic of Germany.

出版信息

Radiat Environ Biophys. 1991;30(4):321-32. doi: 10.1007/BF01210516.

DOI:10.1007/BF01210516
PMID:1961918
Abstract

Measurement methods are described which determine the initial phase of the fluorescence induction kinetics with a maximum time resolution of 10 microseconds simultaneously for the two fluorescence components F685(t) and F730(t) selected by filters at the wavelengths 685 nm and 730 nm, respectively. The excitation light provided by a He-Ne laser (632.8 nm) is switched on within 0.3 microseconds (maximum intensity Ie = 12 mW/cm2). Fo, Fp, and Fs, the initial-, peak-, and steady-state intensity and the initial value Ro of the ratio R(t) = F730(t)/F685(t) can accurately be determined as well as the initial time derivative Fo* of the fluorescence intensity. Fo and Fo* are related to the quantum yield phi a of the antenna and to the photochemical quantum yield phi pc, respectively. Spruce, oak, birch, poplar, and soy bean show a decline of R(t) from Ro to a first minimum Rb at some 10 ms which has a similar value as the second minimum Rp in the time range of seconds. Furthermore, the initial value Ro and the steady-state value Rs of R(t) are also very similar. Measurements on spruce with water deficiency and with varying excitation light intensity Ie show effects on the initial phase of the fluorescence induction kinetics. Further measurements on spruce of different damage classes indicate that for the current year's needles the ratio Fp/Fo is the most sensitive parameter to differentiate between the damage classes and that Fo/Fs and Ro/Rb are also affected. As demonstrated by measurements on leaves of soy beans, the initial decrease of R(t) from Ro to Rb originates from a change of the fluorescence spectrum because no change of the leaf transmission can be observed in the time range between 10 microseconds and 1 ms.

摘要

本文描述了一些测量方法,这些方法能同时以10微秒的最大时间分辨率确定由分别在685纳米和730纳米波长处的滤光片所选择的两个荧光组分F685(t)和F730(t)的荧光诱导动力学的初始阶段。由氦氖激光器(632.8纳米)提供的激发光在0.3微秒内开启(最大强度Ie = 12毫瓦/平方厘米)。可以准确测定初始强度、峰值强度和稳态强度Fo、Fp和Fs,以及比值R(t) = F730(t)/F685(t)的初始值Ro,还有荧光强度的初始时间导数Fo*。Fo和Fo*分别与天线的量子产率φa和光化学量子产率φpc相关。云杉、橡树、桦树、杨树和大豆的R(t)从Ro下降到约10毫秒时的第一个最小值Rb,该值与数秒时间范围内的第二个最小值Rp相似。此外,R(t)的初始值Ro和稳态值Rs也非常相似。对缺水和不同激发光强度Ie的云杉进行测量,结果显示对荧光诱导动力学的初始阶段有影响。对不同损伤等级的云杉进行的进一步测量表明,对于当年的针叶,比值Fp/Fo是区分损伤等级最敏感的参数,并且Fo/Fs和Ro/Rb也会受到影响。正如对大豆叶片的测量所表明的,R(t)从Ro到Rb的初始下降源于荧光光谱的变化,因为在10微秒到1毫秒的时间范围内未观察到叶片透射率的变化。

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1
Measurement of the chlorophyll fluorescence induction kinetics with a 10 microseconds time resolution and its application in the forest decline research.具有10微秒时间分辨率的叶绿素荧光诱导动力学测量及其在森林衰退研究中的应用。
Radiat Environ Biophys. 1991;30(4):321-32. doi: 10.1007/BF01210516.
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Decrease of the chlorophyll fluorescence ratio F690/F730 during greening and development of leaves.叶片变绿和发育过程中叶绿素荧光比率F690/F730的降低。
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本文引用的文献

1
Fluorescence induction kinetics of green and etiolated leaves by recording the complete in-vivo emission spectra.通过记录完整的活体发射光谱来研究绿色和黄化叶片的荧光诱导动力学。
Photosynth Res. 1981 Dec;1(4):233-41. doi: 10.1007/BF00034266.
2
Chlorophyll fluorescence as a tool in plant physiology : II. Interpretation of fluorescence signals.叶绿素荧光作为植物生理学中的一种工具:II. 荧光信号的解读
Photosynth Res. 1984 Jun;5(2):139-57. doi: 10.1007/BF00028527.
3
Chlorophyll fluorescence yield changes as a tool in plant physiology I. The measuring system.
叶绿素荧光产量变化作为植物生理学中的一种工具 一、测量系统
Photosynth Res. 1983 Jan;4(1):361-73. doi: 10.1007/BF00041833.
4
Chlorophyll a fluorescence transients: a fast data acquisition system to facilitate in vivo measurements.叶绿素荧光瞬变:一种快速数据采集系统,便于活体测量。
Photosynth Res. 1983 Jan;4(1):213-27. doi: 10.1007/BF00041817.
5
Fluorescence induction in whole leaves: Differentiation between the two leaf sides and adaptation to different light regimes.整片叶子的荧光诱导:区分叶片两面和适应不同光照条件。
Planta. 1977 Jan;133(2):121-9. doi: 10.1007/BF00391909.
6
[Chlorophyll fluorescence and carbon assimilation. Part XIII. The fluorescence and the photochemistry of plants].[叶绿素荧光与碳同化。第十三部分。植物的荧光与光化学]
Biochem Z. 1960;332:277-92.
7
Analysis of the slow phases of the in vivo chlorophyll fluorescence induction curve. Changes in the redox state of photosystem II electron acceptors and fluorescence emission from photosystems I and II.体内叶绿素荧光诱导曲线慢相分析。光合系统II电子受体氧化还原状态的变化以及光合系统I和II的荧光发射。
Biochim Biophys Acta. 1981 May 13;635(3):542-51. doi: 10.1016/0005-2728(81)90113-4.
8
Application of chlorophyll fluorescence in ecophysiology.叶绿素荧光在生态生理学中的应用。
Radiat Environ Biophys. 1986;25(4):297-308. doi: 10.1007/BF01214643.
9
The fluorescence induction kinetics as a non-destructive tool for investigating spruce treated with ozone.荧光诱导动力学作为一种用于研究经臭氧处理的云杉的非破坏性工具。
Radiat Environ Biophys. 1990;29(1):57-73. doi: 10.1007/BF01211235.