Körner Ch, Farquhar G D, Wong S C
Botanisches Institut, Universität Basel, Schönbeinstrasse 6, CH-4056, Basel, Switzerland.
Plant Environmental Biology, Research School of Biological Sciences, Australian National University, P.O. Box 475, 2601, Canberra, ACT, Australia.
Oecologia. 1991 Sep;88(1):30-40. doi: 10.1007/BF00328400.
In an earlier paper we provided evidence that carbon isotope discrimination during photosynthesis of terrestrial C3 plants decreases with altitude, and it was found that this was associated with greater carboxylation efficiency at high altitudes. Changing partial pressures of CO and O and changing temperature are possible explanations, since influences of moisture and light were reduced to a minimum by selective sampling. Here we analyse plants sampled using the same criteria, but from high and low altitudes along latitudinal gradients from the equator to the polar ends of plant distribution. These data should permit separation of the pressure and temperature components (Fig. 1). Only leaves of fully sunlit, non-water-stressed, herbaceous C3 plants are compared. The survey covers pressure differences of 400 mbar (ca. 5000 m) and 78 degrees of latitude (ca 25 K of mean temperature of growth period). When habitats of similar low temperature (i.e. high altitude at low latitude and low altitude at polar latitude) are compared, discrimination increases towards the pole (with decreasing altitude and thus increasing atmospheric pressure). Latitudinally decreasing temperature at almost constant atmospheric pressure (samples from low altitude) is associated with a decrease in discrimination. So, polar low-altitude plants have δC values half way between humid tropical lowland and tropical alpine plants. It is unlikely that latitudinal changes of the light regime had an effect, since low and high altitude plants show contrasting latitudinal trends in δC although local altitudinal differences in overall light consumption were small. These results suggest that both temperature and atmospheric pressure are responsible for the altitudinal trends in C discrimination. Temperature effects may partly be related to increased leaf thickness (within the same leaf type) in cold environments. Theoretical considerations and laboratory experiments suggest that it is the oxygen partial pressure that is responsible for the pressure related change in discrimination. The study also provided results of practical significance for the use of carbon isotope data. Within a community of C3 plants, discrimination in species of similar life form, exposed to similar light, water and ambient CO conditions ranges over 4‰, with standard deviations for 10-30 species of ±0.6 to 1.2‰. This natural variation has to be taken into account by using a sufficient sample size and standardization of sampling in any attempt at ecological site characterization using carbon isotope data. Evidence of a pronounced genotypic component of this variation in C discrimination in wild C3 plant species is provided. Correlations with dry matter partitioning, mesophyll thickness and nitrogen content are also present.
在一篇早期论文中,我们提供了证据表明陆地C3植物光合作用期间的碳同位素分馏随海拔升高而降低,并且发现这与高海拔地区更高的羧化效率相关。二氧化碳和氧气分压的变化以及温度的变化可能是其原因,因为通过选择性采样将水分和光照的影响降至最低。在此,我们分析了按照相同标准采集的植物样本,但这些样本来自从赤道到植物分布极地末端的沿纬度梯度的高海拔和低海拔地区。这些数据应能区分压力和温度因素(图1)。仅比较完全受阳光照射、无水分胁迫的草本C3植物的叶片。该调查涵盖了400毫巴(约5000米)的压力差和78度的纬度(生长季平均温度约25K)。当比较低温相似的生境(即低纬度高海拔和极地纬度低海拔)时,分馏朝着极地增加(随着海拔降低从而大气压力增加)。在几乎恒定的大气压力下(来自低海拔的样本),纬度降低的温度与分馏降低相关。所以,极地低海拔植物的δC值处于潮湿热带低地植物和热带高山植物之间的中间位置。光照模式的纬度变化不太可能产生影响,因为尽管总体光照消耗的局部海拔差异较小,但低海拔和高海拔植物在δC上呈现出相反的纬度趋势。这些结果表明温度和大气压力均对C分馏的海拔趋势负责。温度效应可能部分与寒冷环境中叶片厚度增加(在同一叶片类型内)有关。理论思考和实验室实验表明,氧气分压是造成与压力相关的分馏变化的原因。该研究还为碳同位素数据的应用提供了具有实际意义的结果。在一个C3植物群落中,生活型相似、暴露于相似光照、水分和环境二氧化碳条件下的物种间分馏范围超过4‰,10 - 30个物种的标准差为±0.6至1.2‰。在利用碳同位素数据进行任何生态场地特征描述的尝试中,必须通过使用足够的样本量和标准化采样来考虑这种自然变异。文中提供了野生C3植物物种中这种C分馏变异存在明显基因型成分的证据。同时也存在与干物质分配、叶肉厚度和氮含量的相关性。