1986
DOI: 10.1007/bf01214643
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Application of chlorophyll fluorescence in ecophysiology

Abstract: In vivo chlorophyll fluorescence measurements have become a valuable tool in ecophysiology. Fluorescence emission spectra are influenced by the reabsorption of the tissue and indicate the composition of the antenna system and are influenced by the chlorophyll content per leaf area. The fluorescence induction kinetics ("Kautsky effect") can be used to study photosynthetic activity. These rapid, non-destructive methods can be applied for ecophysiological field research to check the vitality of plants and to docu… Show more

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Cited by 245 publications
(104 citation statements)
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“…These species are abundant in the High-Arctic tundra in Svalbard, and are also common in the sub-Arctic and alpine environments [35]. The measurements were carried out on green and healthy looking leaves [10,37], resulting in 24, 31, 29 and 28 distinct spectral signatures for Bistorta vivipara, Cassiope tetragona, Dryas octopetala and Salix polaris respectively.…”
Section: In-situ Data Collection and Processingmentioning
confidence: 99%
See 1 more Smart Citation
“…These species are abundant in the High-Arctic tundra in Svalbard, and are also common in the sub-Arctic and alpine environments [35]. The measurements were carried out on green and healthy looking leaves [10,37], resulting in 24, 31, 29 and 28 distinct spectral signatures for Bistorta vivipara, Cassiope tetragona, Dryas octopetala and Salix polaris respectively.…”
Section: In-situ Data Collection and Processingmentioning
confidence: 99%
“…For all analyzed ranges, the results of the NPMANOVA test were significant (p < 0.05). The 400 to 500 nm spectral region allows for an assessment of pigment interaction with light [37,51]. In this region, 12 bands were found to best characterize species that resulted in a 0.90 correctness rate during the LDA stepwise selection of bands.…”
Section: Differences Between Species'mentioning
confidence: 99%
“…After determination of f, wt plant material was frozen and lyophilized. For pigment analysis, chlorophyll a and b and carotenoids of 12 samples per treatment were extracted with DMSO according Hiscox & Israelstam (1979) and calculated according to Lichtenthaler (1987), Carbohydrate content was determined as follows: samples of c. 50 mg of lyophilized material were extracted with 10 mg Polyclar AT (Serva) and 1 -5 ml of hot water in a 2 ml vial at 80 °C for 15 min. After cooling, the samples were shaken for 20 min and centrifuged, the pellet was then washed twice with distilled water, supernatants pooled, lyophilized, and stored at -25 °C,…”
Section: Sampling and Assaysmentioning
confidence: 99%
“…Various studies were conducted on the active measurement of ChlF signals using single point measurements [7][8][9][10][11][12] or ChlF imaging [13][14][15][16][17][18][19][20][21][22][23]. The ChlF principle is based on how light energy, which is absorbed by photosynthetic pigments such as chlorophylls and cartenoids is distributed [10].…”
Section: Introductionmentioning
confidence: 99%