Within-canopy variation in the rate of development of photosynthetic capacity is proportional to integrated quantum flux density in temperate deciduous trees

Authors

  • Ü. NIINEMETS,

    Corresponding author
    1. Department of Plant Physiology, Institute of Molecular and Cell Biology, University of Tartu, Riia 23, Tartu 51010, Estonia,
    2. Centro di Ecologia Alpina, I-38040 Viote del Monte Bondone (TN), Italy,
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  • O. KULL,

    1. Department of Applied Ecology, Institute of Botany and Ecology, University of Tartu, Lai 40, Tartu 51010, Estonia and
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  • J. D. TENHUNEN

    1. LS Pflanzenökologie, University of Bayreuth, D-95440, Bayreuth, Germany
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ABSTRACT

The present study was undertaken to test for the hypothesis that the rate of development in the capacity for photosynthetic electron transport per unit area (Jmax;A), and maximum carboxylase activity of Rubisco (Vcmax;A) is proportional to average integrated daily quantum flux density (Qint) in a mixed deciduous forest dominated by the shade-intolerant species Populus tremula L., and the shade-tolerant species Tilia cordata Mill. We distinguished between the age-dependent changes in net assimilation rates due to modifications in leaf dry mass per unit area (MA), foliar nitrogen content per unit dry mass (NM), and fractional partitioning of foliar nitrogen in the proteins of photosynthetic electron transport (FB), Rubisco (FR) and in light-harvesting chlorophyll-protein complexes (Vcmax;A ∝ MANMFR; Jmax;A ∝ MANMFB). In both species, increases in Jmax;A and Vcmax;A during leaf development were primarily determined by nitrogen allocation to growing leaves, increases in leaf nitrogen partitioning in photosynthetic machinery, and increases in MA. Canopy differences in the rate of development of leaf photosynthetic capacity were mainly controlled by the rate of change in MA. There was only small within-canopy variation in the initial rate of biomass accumulation per unit Qint (slope of MA versus leaf age relationship per unit Qint), suggesting that canopy differences in the rate of development of Jmax;A and Vcmax;A are directly proportional to Qint. Nevertheless, MA, nitrogen, Jmax;A and Vcmax;A of mature leaves were not proportional to Qint because of a finite MA in leaves immediately after bud-burst (light-independent component of MA). MA, leaf chlorophyll contents and chlorophyll : N ratio of mature leaves were best correlated with the integrated average quantum flux density during leaf development, suggesting that foliar photosynthetic apparatus, once developed, is not affected by day-to-day fluctuations in Qint. However, for the upper canopy leaves of P. tremula and for the entire canopy of T. cordata, there was a continuous decline in N contents per unit dry mass in mature non-senescent leaves on the order of 15–20% for a change of leaf age from 40 to 120 d, possibly manifesting nitrogen reallocation to bud formation. The decline in N contents led to similar decreases in leaf photosynthetic capacity and foliar chlorophyll contents. These data demonstrate that light-dependent variation in the rate of developmental changes in MA determines canopy differences in photosynthetic capacity, whereas foliar photosynthetic apparatus is essentially constant in fully developed leaves.

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