1992
DOI: 10.1111/j.1469-8137.1992.tb01133.x
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Effects of ozone on foliar nitrogen metabolism of Pinus taeda L. and implications for carbohydrate metabolism

Abstract: SUMMARYDose-response relationship of ozone effects on foliar nitrogen metabolism of two half-sib families of Pinus taeda L. was studied. Trees were exposed to six ozone concentrations, ranging from 0 2 to 3 times the ambient, for two consecutive growing seasons (1988 and 1989) in open-top chambers. Content of total chlorophyll, soluble protein and soluble amino acids, and activities of glutamine synthetase and glutamate dehydrogenase, were measured in second-flush needles of 1989, harvested in November of 198… Show more

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Cited by 35 publications
(22 citation statements)
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“…Spence et al (1990) reported a reduction in the rate of phloem transport as well as in phloem photosynthate concentration and total carbon transport to the roots. However, Manderscheid et al (1992) concluded from their results with ozone-stressed Pinus taeda L. seedlings that the reduction of carbon allocation to the roots is not due to an inhibited mechanism of phloem loading, but may be explained with the partitioning model postulated by Reynolds and Thornley (1982). According to this model, root growth is favoured by a high ratio of total nonstructural carbohydrates to free amino acids, whereas a low ratio stimulates shoot growth.…”
Section: Discussionmentioning
confidence: 88%
“…Spence et al (1990) reported a reduction in the rate of phloem transport as well as in phloem photosynthate concentration and total carbon transport to the roots. However, Manderscheid et al (1992) concluded from their results with ozone-stressed Pinus taeda L. seedlings that the reduction of carbon allocation to the roots is not due to an inhibited mechanism of phloem loading, but may be explained with the partitioning model postulated by Reynolds and Thornley (1982). According to this model, root growth is favoured by a high ratio of total nonstructural carbohydrates to free amino acids, whereas a low ratio stimulates shoot growth.…”
Section: Discussionmentioning
confidence: 88%
“…Probably also growtb of short roots and formation of mycorrhiza were enhanced to supply enough N for growth and repairing of O3 induced disturbances m protein metabolism (Pell & Dann, 1991). Enhanced N metabolism oi Pinus taeda needles alter exposure to O3 for two growing seasons has been observed by Manderscheid, Jager & Kress (1992), who suggested that nitrogen reallocation occurs to support new growth. Results of the present study suggest that N reallocation tnay be one of the earliest signs of metabolic disturbances caused by Enlarged starcb grains in the needles of fumigated seedlings observed in this experiment may be a sign of initially increased photosynthetic rate (Eanius et al, 1990: Bevers, Riecbers & Temple, 1992, altered carbobydrate metabolism or impaired translocation due to damage of phloem cells caused by Mg deficiency (Eink, 1991), also observed in this study.…”
Section: Discussionmentioning
confidence: 95%
“…Increased N in remaining leaves has also been observed in clonal poplars (PO/)M/)V.V spp.) (Ballach,Oppenheimer&Moori, 1992) and Loblolly pine {Pinus taeda) (Tjoelker & Luxmoore, 1991;Manderscheid, Jager & Kress, 1992) with O.,-induced premature foliar senescence. What is the source of the additional N in these leaves?…”
Section: Discussionmentioning
confidence: 99%
“…What is the source of the additional N in these leaves? Both Ballach et al (1992) and Manderscheid et al (1992) reported evidence of increased proteolytic activity and increased concentrations of soluble amino acids, particularly glutamate and glycine, in O.,-induced senescing leaves. Increased rates of protein turnover in prematurely senescing foliage would increase the availability of N for reallocation to actively growing parts of the plant (Peoples & Dalling, 1988), and would account for the reduced concentration of N in litter from Oa-injured pine seedlings.…”
Section: Discussionmentioning
confidence: 99%