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   <subfield code="a">Cold acclimation and photoinhibition of photosynthesis in Scots pine</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Alla Krivosheeva, Da-Li Tao, Christina Ottander, Gunnar Wingsle, Sylvain Dube, Gunnar Öquist]</subfield>
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   <subfield code="a">Cold acclimation of Scots pine did not affect the susceptibility of photosynthesis to photoinhibition. Cold acclimation did however cause a suppression of the rate of CO2 uptake, and at given light and temperature conditions a larger fraction of the photosystem II reaction centres were closed in cold-acclimated than in nonacclimated pine. Therefore, when assayed at the level of photosystem II reaction centres, i.e. in relation to the degree of photosystem closure, cold acclimation caused a significant increase in resistance to photoinhibition; at given levels of photosystem II closure the resistance to photoinhibition was higher after cold acclimation. This was particularly evident in measurements at 20° C. The amounts and activities of the majority of analyzed active oxygen scavengers were higher after cold acclimation. We suggest that this increase in protective enzymes and compounds, particularly Superoxide dismutase, ascorbate peroxidase, glutathione reductase and ascorbate of the chloroplasts, enables Scots pine to avoid excessive photoinhibition of photosynthesis despite partial suppression of photosynthesis upon cold acclimation. An increased capacity for light-induced de-epoxidation of violaxanthin to zeaxanthin upon cold acclimation may also be of significance.</subfield>
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   <subfield code="a">Springer-Verlag, 1996</subfield>
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   <subfield code="a">Frost hardening</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Low temperature</subfield>
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   <subfield code="a">Photoinhibition</subfield>
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   <subfield code="a">Photosystem II</subfield>
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   <subfield code="a">Pinus</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Scavenging</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">DHAR : dehydroascorbate reductase</subfield>
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   <subfield code="a">Fm : maximal fluorescence when all reaction centres are closed</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Fv/Fm : maximum photochemical yield of PSII</subfield>
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   <subfield code="a">GR : glutathione reductase</subfield>
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   <subfield code="a">Je : rate of photosynthetic electron transport</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">MDAR : monodehydroascorbate reductase</subfield>
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   <subfield code="a">qN : nonphotochemical quenching of fluorescence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">qP : photochemical quenching of fluorescence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">SOD : superoxide dismutase</subfield>
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   <subfield code="a">Krivosheeva</subfield>
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   <subfield code="u">Department of Biophysics, Ural Forest Technology Institute, 620032, Ekaterinburg, Russia</subfield>
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   <subfield code="u">Institute of Applied Ecology, Academia Sinica, P.O. Box 417, 110015, Shenyang, China</subfield>
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   <subfield code="a">Ottander</subfield>
   <subfield code="D">Christina</subfield>
   <subfield code="u">Department of Plant Physiology, University of Umeå, S-901 87, Umeå, Sweden</subfield>
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   <subfield code="a">Dube</subfield>
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