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   <subfield code="a">10.1007/s11099-015-0148-8</subfield>
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   <subfield code="a">Girdling-induced Alhagi sparsifolia senescence and chlorophyll fluorescence changes</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[G. Tang, X. Li, L. Lin, F. Zeng, Z. Gu]</subfield>
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   <subfield code="a">Senescence constitutes the final stage of a plant organ and tissue development and is a subject to gene control and strict regulation. By the late growing season, when Alhagi sparsifolia entered the natural senescence period, a girdling treatment was carried out on the phloem to increase the sugar content in leaves and to investigate carbohydrate-induced leaf senescence. After the semi-girdling and full-girdling treatment, organic matter could not leave leaves due to the destruction of sieve tubes. This led to constantly increasing sugar contents in leaves. Girdling was shown to greatly accelerate the senescence of plants. In girdled leaves, chlorophyll (Chl) a, Chl b, carotenoids (Car), and both ratios of Chl a/b and Chl/Car were significantly reduced. On the donor side of PSII, the oxygen-evolving complex was inhibited under high concentrations of carbohydrates, which was manifested as the emergence of the K phase in fluorescence kinetic curves. On the acceptor side of PSII, the high carbohydrate content also led to the disruption of electron transport and reduced light-use efficiency, which was manifested as a reduction in numerous fluorescence parameters. We believe that the emergence and development of plant senescence was not necessarily induced by the high content of carbohydrates, because even a decrease in the carbohydrate concentration could not stop the senescence process. Although the high content of carbohydrates in plants could induce plant senescence, this kind of senescence was likely a pathological process, including degradations of physiological functions.</subfield>
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   <subfield code="a">The Institute of Experimental Botany, 2015</subfield>
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   <subfield code="a">carbon</subfield>
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   <subfield code="a">nutrient cycling</subfield>
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   <subfield code="a">photosynthetic apparatus</subfield>
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   <subfield code="a">photosynthetic pigment</subfield>
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   <subfield code="a">reactive oxygen</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">stress</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Car : carotenoids</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Chl : chlorophyll</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">CK : control</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">DM : dry mass</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">FG : full-girdling</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">FM : fresh mass</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Fv/Fm : maximal quantum yield of PSII photochemistry</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">MDA : malondialdehyde</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">M0 : approximated initial slope of the fluorescence transient</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">OEC : oxygen-evolving complex</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">PIabs : performance index on absorption basis</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">P N : net photosynthetic rate</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Pro : proline</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">PQ : plastoquinone</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">QA : primary quinone acceptor of PSII</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">QB : secondary quinone acceptor of PSII</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">SE : standard error</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">SG : semigirdling</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Sm : normalized total complementary area above the O-J-I-P transient</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Ψ0 : probability that a trapped exciton moves an electron into the electron transport chain beyond QA − (at t = 0)</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">φE0 : quantum yield for electron transport (at t = 0)</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Tang</subfield>
   <subfield code="D">G.</subfield>
   <subfield code="u">State Key Laboratory of Desert and Oasis Ecology, Xinjiang Institute of Ecology and Geography, Chinese Academy of Sciences, 830011, Urumqi, China</subfield>
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   <subfield code="a">Li</subfield>
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   <subfield code="t">Photosynthetica</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
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