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   <subfield code="a">Is long-lived foliage in Picea mariana an adaptation to nutrient-poor conditions?</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Ken Greenway, S. Macdonald, Victor Lieffers]</subfield>
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   <subfield code="a">Summary: This study evaluated the contribution of different ages of foliage to the nutrient and carbon balance of black spruce (Picea mariana (Mill.) B.S.P.) from a nutrient-poor peatland in Alberta. Seasonal patterns of foliar nitrogen and phosphorus concentration and content were examined in six needle cohorts up to 10 years old. Trees were treated to simulate excess nutrient deficiency (removal of all one-year-old foliage), nutrient excess (fertilized with 250, 50, 100 kg ha−1 NPK split application in June and July), or left as controls. Gas exchange (net assimilation-Na, stomatal conductance-gs, mesophyll conductance-gm, water-use efficiency-WUE, dark respiration-RS) was measured on six different needle cohorts in several control trees in 1989 and 1990. Nitrogen and phosphorus concentration decreased with needle age. Foliar nutrient concentration fell from April to June and then was stable until September except for the fertilized trees where it increased. There was no evidence of greater than normal retranslocation of nutrients from older needles for defoliated trees or greater than normal nutrient loading in older needles of fertilized trees. NA, gs, gm, WUE, and RS were similar for all needles up to six or eight years old, these older needles having NA of 65% of current needles and similar RS. The results do not support to conclusion that older needles of black spruce are retained as an adaptation to nutrient stress. It does not appear that older needles serve as a nutrient storage site in conditions of excess nutrient availability or a greater than normal nutrient source during times of excess nutrient deficiency. It appears that the maintenance of long-livedfoliage in black spruce does not provide for greater flexibility in tree nutrient allocation. Their contribution to the carbon balance of the tree seems to be sufficient to explain their retention.</subfield>
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   <subfield code="a">Springer-Verlag, 1992</subfield>
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   <subfield code="a">Foliar nutrient retranslocation</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Needle age</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Photosynthesis</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Nitrogen</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Phosphorus</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Respiration</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Greenway</subfield>
   <subfield code="D">Ken</subfield>
   <subfield code="u">Department of Forest Science, University of Alberta, T6G 2H1, U, Edmonton, Alberta, Canada</subfield>
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   <subfield code="a">Macdonald</subfield>
   <subfield code="D">S.</subfield>
   <subfield code="u">Department of Forest Science, University of Alberta, T6G 2H1, U, Edmonton, Alberta, Canada</subfield>
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   <subfield code="t">Oecologia</subfield>
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   <subfield code="g">91/2(1992-08-01), 184-191</subfield>
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