Discussion. The observed drop in nitrate content (see Fig. 1) could be relatedto the increased activity of NR under conditions of enhanced photosynthesis intensityand due to maintaining phytochrome in the physiologically active Pfr isoform.Low radiant heat of solid-state sources of light allows using effectively much higherPPFs than those under conventional discharge or fluorescent lamps. The observedincrease in concentration of carbohydrates in the treated plants from the th<strong>ir</strong>d lightingday (see Fig. 3) is probably due to the increased photosynthesis intensity. Priceet al. (2004) showed that glucose has a stronger effect on the regulation of genesassociated with nitrogen metabolism than nitrogen supply. Besides, such an increasein carbohydrate concentration is favourable in terms of self-supporting NR activitythrough stimulation of gene expression (Cheng et al., 1992; Lillo and Appenroth,2001). Moreover, carbohydrates are able to compete light in stimulating expressionof genes involved in nitrogen assimilation (Thum et al., 2003). However, the supplementallighting with red LEDs leads to increased carbohydrate content, especially ofsucrose (see Fig. 3), and this can be a signal inducing the processes of senescence(Causin et al., 2006; Munde-Bosch, 2007). The sucrose metabolism is a physiologicalsignal affecting further metabolic processes, (Koch, 2004) nutrient and gustatoryproperties. However, in this case low ratio of hexoses and sucrose (see Fig. 3) couldaccelerate the induction of senescence mechanism. Such carbohydrate distributionin lettuce leaves was conditioned not only by supplemented red light alone, but alsoby other env<strong>ir</strong>onmental conditions, which affected decrease of photosynthesis systemaction and thereof processes of senescence were induced. Besides, according toWingler and co-workers (Wingler et al., 2006), too early senescence would reduceplant’s capacity to assimilate CO 2, whereas too late senescence would interfere withnutrient remobilisation, thereby compromising photosynthetic activity in the youngleaves and reproductive success. Other authors propose that leaf senescence can beinduced by low nutrient supply (Ono et al., 1996) or it can be maintained by carbonbalance of a plant (Wingler et al., 2006). Otherwise, Wingler and co-workers assumethat sucrose did not accumulate during developmental senescence (Wingler et al.,2006). The question remains – what causes strong accumulation of hexoses despitethe decline in photosynthetic carbon assimilation in senescing leaves? A possiblesource of hexoses is the breakdown of starch. In addition, Jongebloed et al. (2004)have shown that phloem blockage by callose deposition could lead to an age-dependedsugar accumulation.Although it is maintained that red light makes positive effect on the formationand action of photosynthetic system (Spalding and Folta, 2005), according to ourresults, strong accumulation of carotenoids and thereof high ratio of carotenoids andsum of chlorophylls a and b and suspended growth (see Fig. 4) allow to presume thatthe excess of red light induced the senescence processes. According to Martin et al.(2002), the regulation of photosynthesis and plant development appears to dependon the carbon/nitrogen ratio instead of carbohydrate alone. These carbon/nitrogeninteractions are likely to play an important role in the regulation of leaf senescence.Agreeably with other authors (Diaz et al., 2005), sugar and nitrogen contents showdistinct changes during leaf senescence, with sugars accumulation (see Fig. 3) and116
nitrate decline (see Fig. 1).The tendency of increase in the vitamin C content in LED-treated lettuce leavesin contrary to reference ones was observed, and thus coheres with the faster senescenceprocesses. Besides, vitamin C is not only an important nutrient but also plays amajor role in the protection of plants against photo-oxidative stress, photoprotection,and phytohormones action (Conklin, 2001, Davey et al., 2000; Pastori et al., 2003).Interestingly, a noticeable increase in vitamin C content (see Fig., 2) is observedin lettuce leaves where LED treatment invoked an increase in the concentration ofcarbohydrates (see Fig. 3). However, Ono et al. (2001) suppose that the induction ofsenescence by red light could not be caused by photo-oxidative stress, since even higherlight intensity in his experiment was low compared with natural conditions. Instead,illumination-depended changes in carbohydrate content (see Fig. 3) and in carotenoid/chlorophyll ratio (see Fig. 4) may have influenced senescence.Conclusions. Nitrate decline, sugar and carotenoid accumulation, low hexoses/sucrose ratio, in supplemented red LEDs treatment induces lettuce leaves senescencethrough sugar signalling pathways. In addition, env<strong>ir</strong>onmental conditions may regulatesenescence through pathways that are independent from photosynthesis and itsprimary metabolites. An increase in vitamin C concentration can trigger senescencethrough photo-oxidative stress. This achieved effect by generating photo stress inlettuce leaves accelerated senescence and led to manipulate the synthesis of primaryand secondary metabolites to economically advantage d<strong>ir</strong>ection.Acknowledgements. This study was supported by Lithuanian Science and Studyfoundation under the high technology project PHYTOLED (Nr. B24-2007).Gauta 2009 05 05Parengta spausdinti 2009 06 05References1. Andrews M. 1986. The partitioning of nitrate assimilation between root and shootof higher plants: mini-review. Plant Cell Env<strong>ir</strong>onment, 9: 511–519.2. Casal J. J., Yanovsky M. J. 2005. Regulation of gene expression by light.International Journal of Development Biology, 49: 501–511.3. Causin H. F., Jauregui R. N., Barniex A. J. 2006. The effect of light spectralquality on leaf senescence and oxidative stress in wheat. Plant Science, 171:24–53.4. Cheng C. L, Acedo G. N., Cristinsin M., Conkling M. A.. 1992. Sucrose mimicsthe light induction of Arabidopsis nitrate reductase gene transcription. Proc.Natl. Acad. Sci. USA, 89: 1 861–1 864.5. Conklin P. L. 2001. Recent advantages in the role and biosynthesis of ascorbicacid in plants. Plant Cell Env<strong>ir</strong>onment, 24: 383–394.117
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SCIENTIFIC WORKS OF THE LITHUANIAN
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Table 1. Dates of blooming periods
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Average yield of apple cultivars ra
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Table 4. Harvest date, end of stora
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10. Sasnauskas A., Gelvonauskienė
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(Curran ir kt.,1995; Filella ir kt.
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yra mažesnis. Vis dėlto chlorofil
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Literatūra1. Asada T., Ogasawara M
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1 pav. Laikotarpio nuo seno sodo i
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4 pav. Laikotarpio nuo seno sodo i
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9. Leinfelder M. M., Merwin I. A. 2
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availability of nutrients and incre
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Table 2. Amount of microelements (m
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of P was determined in the apple-tr
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References1. Adriano D. C. 1986. Tr
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LIETUVOS SODININKYSTĖS IR DARŽINI
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SOD-1 izoformos aktyvumas yra dides
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Palyginę 2007 ir 2008 metų duomen
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action of berries of these cultivar
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1999; Litwińczuk, 2002). Duomenų
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2 pav. Kanamicino įtaka vienam eks
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eksplantus - mikroūglius ir hipoko
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12. Tang H., Ren Z., Reustle G., Kr
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Ribes, Prunus, Sambucus genčių au
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koncentracijos skatino svogūno mer
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5. Glinska S., Bartczak M., Oleksia
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LIETUVOS SODININKYSTĖS IR DARŽINI
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Tyrimais nustatyta, kad organogenez
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Žalios spalvos augalai regeneranta
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9. Mashayekhi M., Shakib A. M., Ahm
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ATMINTINĖ AUTORIAMS, RAŠANTIEMSĮ
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Bandymų veiksnių gradacijos lente
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GUIDELINES FOR THE PREPARATION AND
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they should be understandable. The
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Turinys - ContentsA. Sasnauskas, D.
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S. Sakalauskienė, A. Brazaitytė,