1981
DOI: 10.1007/bf02878418
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Accumulation of phenolics and growth rate of barley seedlings (Hordeum vulgare L.)

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Cited by 8 publications
(7 citation statements)
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“…Higher accumulation of phenolics mainly consisting of SA was detected in barley seedlings at low temperature (5 °C), but seedling growth showed an opposite trend. 51 Moreover, this study elucidated that peroxidase and phenylalanine ammonialyase activated more at low temperature were responsible for SA accumulation in barley seedlings. On the other hand, adaptation of barley plants under high temperature has been observed by Mikkelsen et al 52 In addition to SA, high temperature exposure also increased the accumulation of other flavonoid families, such as lutonarin in barley, which suggested their potential involvement in the plant response to unfavorable temperature conditions.…”
Section: Against Environmental Stressesmentioning
confidence: 83%
“…Higher accumulation of phenolics mainly consisting of SA was detected in barley seedlings at low temperature (5 °C), but seedling growth showed an opposite trend. 51 Moreover, this study elucidated that peroxidase and phenylalanine ammonialyase activated more at low temperature were responsible for SA accumulation in barley seedlings. On the other hand, adaptation of barley plants under high temperature has been observed by Mikkelsen et al 52 In addition to SA, high temperature exposure also increased the accumulation of other flavonoid families, such as lutonarin in barley, which suggested their potential involvement in the plant response to unfavorable temperature conditions.…”
Section: Against Environmental Stressesmentioning
confidence: 83%
“…Trade-offs between primary and secondary metabolism are well documented in cell cultures (Phillips and Henshaw, 1977;Lindsey and Yeoman, 1983;Collin, 1987) and at the whole plant level. Many intraspecific comparisons document physiological trade-offs between growth rate and secondary metabolism in both wild and crop species (Hanover , 1966a;del Moral, 1972;Mooney and Chu, 1974;Podstolski et al, 1981;Krischik and Denno, 1983;Lincoln, 1985, 1989a;Waring et al, 1985;Coley, 1986;Larsson et al, 1986;Lorio and Sommers, 1986;Bryant, 1987;Bryant, Chapin, Reichardt, and Clausen, 1987;Bryant, Clausen, Reichardt, McCarthy, and Werner, 1987;Lightfoot andWhitford, 1987, 1989;Appleton and van Staden, 1989;Glyphis and Put tick, 1989;Hrutfiord and Gara, 1989;Margna et al, 1989). Bjorkman and Anderson (1990) have also documented a trade-off between growth and structural defenses (the elaboration of which diverts resources from the production of leaf area) in South American blackberry (Rubus bogotensis).m olls, in that the translocation of resources within and among them can be restricted (Watson and Casper, 1984:;Dickson, 1989;Wardlaw, 1990).…”
Section: Whole-plant Resource Trade-offs Constrain Secondary Metabolismmentioning
confidence: 99%
“…À côté du rôle des tanins dans la réaction contre les attaques parasitaires (KEMP et BURDEN, 1986), ces composés interviendraient également dans le cas de stress induit par les faibles températures. Leur synthèse serait alors favorisée par l'action stimulatrice du froid sur la synthèse de la phénylalanine ammonia-lyase (PAL) (PODSTOLSKI et al, 1981 ;GRAHAM et PETTERSON et al, 1982). À cela, s'ajoute la disponibilité, en quantité suffisante, des sucres solubles, produits de l'hydrolyse de l'amidon, qui interviennent plus ou moins directement dans la synthèse des tanins (MINAMIKAWA et YOSHIDA, 1980 ;WAFFO-TUEGO, 1996 ;.…”
Section: Discussion Et Conclusionunclassified