Certain dicotyledon families characteristically have tracheids as their imperforate tracheary element type. Of these, six families are anomalous by having septate (or nonseptate but living) fiber-tracheids or libriform fibers coexisting with the tracheids in some species or genera (Austrobaileyaceae, Celastraceae, Convolvulaceae, Ericaceae, and Grossulariaceae, and Rosaceae). Data from the literature and original data on wood anatomy of these families are presented. A theory of tracheid dimorphism is developed to account for these instances of tracheids combined with fiber-tracheids or libriform fibers. According to this theory, septate or living fiber-tracheids or libriform fibers are produced in addition to tracheids, starting with ancestors that contain tracheids as the only imperforate tracheary element type, in response to selection for a rapidly increased photosynthate storage capacity, while maintaining the advantage of tracheids in providing conductive safety. Borders are phyletically lost rapidly on the septate (or nonseptate but living) imperforate tracheary elements because they are not water-conducting cells. Genera cited in this stud y can be ranged into a phyletic series with respect to differentiation from the hypothetical monomorphic-tracheid ancestors with respect to (I) loss of borders on pits of the septate or living elements; (2) distribution of tracheids with respect to vessels; and (3) retention of axial parenchyma. Austrobaileya is the most primitive genus in these respects, while genera such as Holodiscus and Spiraea are specialized. Tracheid dimorphism is compared to vessel dimorphism, fiber-tracheid dimorphism, fiber dimorphism, and the dimorphism related to origin of vessels. All these pathways except the last named one are confined to small numbers of families, and are considered minor trends superimposed on the major trends described by I. W. Bailey and coworkers. Basic to all of the dimorphic behaviors described is selection for two divergent cell types as a way of performing two distinctive wood functions.
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机译:某些双子叶植物的特征是气孔是其无孔气管元素类型。其中有六个科是异常的,它们在某些物种或属中(奥贝贝科,Celastraceae,旋花科,Ericaceae和Ecosaceae和Grossulariaceae和蔷薇科)分别存在(或不分隔但存活的)纤维气管或游离状纤维与气管共存。介绍了来自这些家族的文献数据和有关木材解剖的原始数据。发展了气管二态性的理论来解释这些气管与纤维-气管或libriform纤维结合的情况。根据该理论,除了选择管胞外,还产生分隔的或活体的纤维管胞或libriform纤维,从包含管胞作为唯一无孔气管元素类型的祖先开始,以响应对快速增加的光合产物存储能力的选择,同时保持气管在提供导电安全性方面的优势。由于分隔壁不是导水细胞,因此在分隔的(或非分隔但活着的)无孔的气管元件上迅速失去了边界。关于(I)隔室或活体元素凹坑上边界的缺失,与假想的单形气管祖先的分化有关,本研究中引用的属可以分为种系。 (2)相对于船只的气管分布; (3)保留轴向实质。在这些方面,Austrobaileya是最原始的属,而Holodscus和Spiraea等属则是专门的。将气管二态性与血管二态性,纤维-气管二态性,纤维二态性以及与血管起源相关的二态性进行比较。除姓氏最后一个以外,所有这些途径都局限于少数家庭,被认为是微小的趋势,与I. W. Bailey及其同事所描述的主要趋势相叠加。所描述的所有双态行为的基础是选择两种不同的细胞类型,以执行两种独特的木材功能。
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