Department of Plant Ecology, Forestry and Forest Products Research Institute (FFPRI), Ibaraki 305-8687, Japan.
Tree Physiol. 2011 Sep;31(9):976-84. doi: 10.1093/treephys/tpr016. Epub 2011 Apr 4.
Hydraulic limitations associated with increasing tree height result in reduced foliar stomatal conductance (g(s)) and light-saturated photosynthesis (A(max)). However, it is unclear whether the decline in A(max) is attributable to height-related modifications in foliar nitrogen concentration (N), to mesophyll conductance (g(m)) or to biochemical capacity for photosynthesis (maximum rate of carboxylation, V(cmax)). Simultaneous measurements of gas exchange and chlorophyll fluorescence were made to determine g(m) and V(cmax) in four height classes of Pinus densiflora Sieb. & Zucc. trees. As the average height of growing trees increased from 3.1 to 13.7 m, g(m) decreased from 0.250 to 0.107 mol m(-2) s(-1), and the CO(2) concentration from the intercellular space (C(i)) to the site of carboxylation (C(c)) decreased by an average of 74 µmol mol(-1). Furthermore, V(cmax) estimated from C(c) increased from 68.4 to 112.0 µmol m(-2) s(-1) with the increase in height, but did not change when it was calculated based on C(i). In contrast, A(max) decreased from 14.17 to 10.73 µmol m(-2) s(-1). Leaf dry mass per unit area (LMA) increased significantly with tree height as well as N on both a dry mass and an area basis. All of these parameters were significantly correlated with tree height. In addition, g(m) was closely correlated with LMA and g(s), indicating that increased diffusive resistance for CO(2) may be the inevitable consequence of morphological adaptation. Foliar N per unit area was positively correlated with V(cmax) based on C(c) but negatively with A(max), suggesting that enhancement of photosynthetic capacity is achieved by allocating more N to foliage in order to minimize the declines in A(max). Increases in the N cost associated with carbon gain because of the limited water available to taller trees lead to a trade-off between water use efficiency and photosynthetic nitrogen use efficiency. In conclusion, the height-related decrease in photosynthetic performance appears to result mainly from diffusive resistances rather than biochemical limitations.
与树木增高相关的水力限制导致叶片气孔导度(g(s))和光饱和光合作用(A(max))降低。然而,目前尚不清楚 A(max) 的下降是归因于与高度相关的叶片氮浓度(N)的变化,还是归因于叶肉导度(g(m))或光合作用的生物化学能力(羧化的最大速率,V(cmax))。对 4 个不同高度的红松(Pinus densiflora Sieb. & Zucc.)树木进行了气体交换和叶绿素荧光的同步测量,以确定 g(m)和 V(cmax)。随着生长树木的平均高度从 3.1 米增加到 13.7 米,g(m)从 0.250 降至 0.107 mol m(-2) s(-1),细胞间隙(C(i))至羧化部位(C(c))的 CO(2)浓度平均降低了 74 µmol mol(-1)。此外,C(c) 估算的 V(cmax)随高度增加从 68.4 增加到 112.0 µmol m(-2) s(-1),但基于 C(i)计算时并未改变。相比之下,A(max)从 14.17 降至 10.73 µmol m(-2) s(-1)。单位叶面积的干质量(LMA)随树高以及干质量和面积基础上的 N 显著增加。所有这些参数都与树高显著相关。此外,g(m)与 LMA 和 g(s)密切相关,表明 CO(2)扩散阻力的增加可能是形态适应的必然结果。单位面积叶片 N 与基于 C(c)的 V(cmax)呈正相关,而与 A(max)呈负相关,这表明通过将更多的 N 分配到叶片来增强光合能力,以最小化 A(max)的下降。由于高大树木可获得的水分有限,与碳获取相关的氮成本增加会导致水分利用效率和光合氮利用效率之间的权衡。总之,与高度相关的光合作用性能下降似乎主要是由于扩散阻力,而不是生化限制。