Hejnowicz Z
Department of Biophysics and Cell Biology, Silesian University, Katowice, Poland.
Planta. 1997 Sep;203(Suppl 1):S136-46. doi: 10.1007/pl00008102.
Tissue stresses, which occur in turgid herbaceous stems, both elongating and non-elongating. and tree growth stresses (TGSs) which occur in woody stems, are similar in that (i) they form self-equilibrating patterns of stresses (tensile and compressive) in stems, and (ii) the asymmetric, graviresponsive change in the pattern tends to bend the stem. The longitudinal tensile tissue stress (TS) which occurs in the outer layers of turgid stems is a few times higher than the osmotic pressure of cell sap in such a layer. Usually it is considered that TSs originate from the differential growth of tissues in a stem; however, physical analysis of a turgid stem model has shown that TSs are an unavoidable physical consequence of the variation in structural characteristics of cell layers or vascular strands in turgid stems. The model applied to the sunflower hypocotyl gives forces which fit well to those measured. The structural characteristics are sufficient to explain fully the TSs which exist in turgid stems. Differential growth is not necessary in this respect. Examination of the model shows also that the longitudinal elastic strain of all cell walls in a turgid stem is the same at a given stem level regardless of wall thickness, i.e. the structure-based TSs compensate for the variation in turgor-induced wall stress in single cells with variable diameter and wall thickness. The importance of this compensation for the anisotropy of wall stresses is presented. The forces which generate TSs exert bending moments which are high but they sum mutually to zero in a vertical stem. In gravistimulated turgid stems of Reynoutria, the TSs decrease considerably on the lower side while those on the upper side remain unaltered. The consequences of this asymmetric change for gravitropic bending are analysed. Tree growth stresses arise in a process by which new cells added by the cambium to the secondary xylem tend to shrink longitudinally (except compression wood) during maturation of the cell walls. The pattern of TGSs is characterized by tensile or compressive stress in the peripheral or the core wood, respectively. An asymmetrical pattern of TGSs due to asymmetrical deposition of wood results in a bending moment which equilibrates the bending moment caused by the weight of a lateral branch. In response to a gravity-derived stimulus the TGS pattern may be modified by asymmetric formation of reaction wood which differs histologically from normal wood: tension wood in many arborescent angiosperms, and compression wood in conifers. The formation and functioning of the reaction wood is discussed.
组织应力出现在膨压状态的草本茎中,包括正在伸长和不再伸长的茎。树木生长应力(TGSs)出现在木质茎中,二者相似之处在于:(i)它们在茎中形成自平衡的应力模式(拉伸和压缩);(ii)模式中不对称的、重力响应性变化往往会使茎弯曲。膨压茎外层出现的纵向拉伸组织应力(TS)比该层细胞液的渗透压高几倍。通常认为组织应力源于茎中组织的差异生长;然而,对膨压茎模型的物理分析表明,组织应力是膨压茎中细胞层或维管束结构特征变化不可避免的物理结果。应用于向日葵下胚轴的模型得出的力与测量值非常吻合。结构特征足以充分解释膨压茎中存在的组织应力。在这方面,差异生长并非必要条件。对模型的研究还表明,在给定的茎水平上,膨压茎中所有细胞壁的纵向弹性应变相同,与细胞壁厚度无关,即基于结构的组织应力补偿了单个细胞中膨压诱导的壁应力随直径和壁厚变化的情况。阐述了这种补偿对壁应力各向异性的重要性。产生组织应力的力会施加很高的弯矩,但在垂直茎中它们相互抵消为零。在重力刺激下的虎杖膨压茎中,下侧的组织应力大幅降低,而上侧的组织应力保持不变。分析了这种不对称变化对向重力性弯曲的影响。树木生长应力产生于形成层向次生木质部添加的新细胞在细胞壁成熟过程中往往纵向收缩(除受压木外)的过程。树木生长应力模式的特征分别是外周木材或芯材中的拉伸或压缩应力。由于木材不对称沉积导致的树木生长应力不对称模式会产生一个弯矩,该弯矩平衡由侧枝重量引起的弯矩。响应重力衍生的刺激,树木生长应力模式可能会因反应木的不对称形成而改变,反应木在组织学上与正常木材不同:许多乔木被子植物中的拉力木和针叶树中的受压木。讨论了反应木的形成和功能。