1997
DOI: 10.1023/a:1006859917345
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Changes in French bean cotyledon composition associated with modulated life-span

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Cited by 13 publications
(6 citation statements)
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“…The latter have been mostly reported in a context with relatively high irradiance, which induces leaves senescence (Biswal and Biswal 1984, Noodén et al 1996, Weaver and Amasino 2001. In our experiments cotyledon senescence induced by continuous irradiation occurred earlier than natural senescence: the life span of cotyledons of C plants was 16 d, of CL plants only 13 d. Chlorophyll (Chl) content is a generally used marker of leaf senescence (Thimann 1980, Matile 1992, Hillman et al 1994, Wilhelmová et al 1997. It can be assumed that the onset of senescence occurred after the 13 th day in C plants because from the 13 th day both Chl content and photochemical efficiency (expressed as F v /F m ratio) decreased.…”
Section: Discussionmentioning
confidence: 71%
See 1 more Smart Citation
“…The latter have been mostly reported in a context with relatively high irradiance, which induces leaves senescence (Biswal and Biswal 1984, Noodén et al 1996, Weaver and Amasino 2001. In our experiments cotyledon senescence induced by continuous irradiation occurred earlier than natural senescence: the life span of cotyledons of C plants was 16 d, of CL plants only 13 d. Chlorophyll (Chl) content is a generally used marker of leaf senescence (Thimann 1980, Matile 1992, Hillman et al 1994, Wilhelmová et al 1997. It can be assumed that the onset of senescence occurred after the 13 th day in C plants because from the 13 th day both Chl content and photochemical efficiency (expressed as F v /F m ratio) decreased.…”
Section: Discussionmentioning
confidence: 71%
“…Jantar) plants were grown in sand in plastic pots in a growth chamber (Klimabox 1300, Kladno, Czech Republic). The control plants (C plants) were grown under 16-h photoperiod, temperature 24/18 °C, air humidity 60/80 % and irradiation of 220 µmol(photon) m -2 s -1 (for detail see Wilhelmová et al 1997). Continuously irradiated plants (CL plants) were grown under continuous irradiation 220 µmol m -2 s -1 , temperature 24 °C and air humidity 60 %.…”
Section: Methodsmentioning
confidence: 99%
“…LFP assay: LFP were estimated in lipophilic extracts of whole cotyledons in chloroform after HPLC (Shimadzu LC9, Kyoto, Japan) resolution. They were characterized by blue fluorescence emission after excitation in UV using fluorimeter Perkin Elmer LS5 (Boston, USA; Wilhelmová et al 1997). The fluorometer was calibrated with the standard No.…”
Section: Determination Of Cytokininsmentioning
confidence: 99%
“…In senescent cotyledons, the percentage of LFP decreased in cytoplasm and increased in microsomal membranes (Hudák et al 1995). We have characterized LFP in ageing of bean cotyledons and their time-course after decapitation of the plant epicotyl (Wilhelmová et al 1997).…”
Section: Introductionmentioning
confidence: 99%
“…These changes help in scavenging free radicals and harmful oxidants in plant cells, thereby protecting them from oxidative damage . Second, under conditions of limited soil moisture, plant metabolism undergoes changes at the developmental, physiological, and molecular levels, resulting in reduced photosynthetic rates, alterations in photosynthetic proton and electron transport, and decreased carbon oxidation and assimilation. , CKs have multiple effects on plant photosynthesis, and they can promote chloroplast differentiation, transformation, and division, increase the number of chloroplasts, promote the formation of grana, and elevate the levels of photosynthetic pigments such as chlorophyll and carotenoids. Moreover, CKs can enhance photosynthetic rates, photochemical quenching, and the maximum photochemical efficiency of photosystem II . During drought stress, CKs can slow down the decline in chlorophyll content, the reduction in grana formation, and the decrease in photosynthetic parameters …”
Section: Introductionmentioning
confidence: 99%