细根周转对森林生态系统碳地下分配和养分循环具有重要影响,而衰老是细根周转过程中最重要的阶段。根据“源一汇”理论,细根衰老受碳向细根分配的影响。为此,该研究通过控制水曲柳(Fraxinus mandshurica)苗木向根系的碳分配的遮荫处理试验,采用树木生理分析技术,重点研究了在光合产物供应停止情况下水曲柳幼苗根系的生理变化(即根尖、1级根到3级根的细胞活力、可溶性糖含量、可溶性蛋白含量和膜透性的变化)。目的是从生理水平上证实:1)碳分配对细根衰老产生怎样的影响;2)细根衰老的顺序是否与分支顺序相反。实验结果表明,遮荫处理使细根活力、可溶性糖含量、可溶性蛋白含量显著降低和膜透性增大,导致细根出现明显衰老。从根系顶端向基部随着根序增加,细胞活力、可溶性糖含量和可溶性蛋白含量提高,膜透性降低,从生理水平上表明细根衰老具有逐渐变化的顺序性,并且这种顺序性与根发育的顺序性相反。
Fine root production and mortality play essential roles in carbon allocation and nutrient cycling in forest ecosystems. Despite the ecological importance of fine root turnover and the tremendous research effort on this subject, our knowledge of fine root mortality is still limited because little is understood on processes of fine root senescence. The most important function of fine roots is nutrient and water acquisition from the soil. Thus, to perform this function, carbohydrates fixed in leaves must be transported belowground to build the root system and support their functions, such as root elongation, nutrient and water uptake, and support microbes in the rhizosphere. More recently, studies on root longevity and root orders have found that first-order roots at the distal end of a root system are thinner in diameter and shorter in life-span than higher order roots. Also, fine root mortality was caused mainly by exhaustion of carbohydrates, suggesting that carbon allocation to fine roots may be an important factor affecting the senescence and mortality of fine roots. The objective of this study was to answer the following two questions: how does senescence of fine roots with different orders responds to reduced C allocation and what is the sequence of senescence from first-order to higher order roots? This study was conducted in greenhouse on the campus of Northeast Forestry University during growing season from April to October in 2004 using Fraxinus mandshurica seedlings as experimental materials. Three one-year-old F. mandshurica seedlings were planted in each of 30 pots with crop soil in April 2004. At the end of June, two light treatments were carried out. Seedlings in 15 pots were grown under natural sunlight (1 000 μmol·m^-2· s^-1) used as controls, and the other 15 pots were completely shaded. After treatments for 30, 60 and 120 d, roots in five pots were carefully excavated, washed and separated into root tips, first-order, second-order and third-order roots. Four physiological indices (i