Tracheid structure in a primitive extant plant provides an evolutionary link to earliest fossil tracheids

Citation
Me. Cook et We. Friedman, Tracheid structure in a primitive extant plant provides an evolutionary link to earliest fossil tracheids, INT J PL SC, 159(6), 1998, pp. 881-890
Citations number
51
Categorie Soggetti
Plant Sciences
Journal title
INTERNATIONAL JOURNAL OF PLANT SCIENCES
ISSN journal
10585893 → ACNP
Volume
159
Issue
6
Year of publication
1998
Pages
881 - 890
Database
ISI
SICI code
1058-5893(199811)159:6<881:TSIAPE>2.0.ZU;2-L
Abstract
Most attempts to understand the early evolution of tracheids have centered on fossil Silurian and Devonian vascular plants, and these efforts have led to a wealth of new information on early water-conducting cells. All of the se early tracheids appear to possess secondary cell wall thickenings compos ed of two distinct layers: a layer adjacent to the primary cell wall that i s prone to degradation (presumably during the process of fossilization) and a degradation-resistant (possibly lignified) layer next to the cell lumen. Developmental studies of secondary wall formation in tracheary elements of extant vascular plants have been confined to highly derived seed plants, a nd it is evident that the basic structure of these secondary cell wall thic kenings does not correspond well to those of tracheids of the Late Silurian and Early Devonian. Significantly, secondary cell wall thickenings of trac heary elements of seed plants are not known to display the coupled degradat ion-prone and degradation-resistant layers characteristic of tracheids in e arly tracheophytes. We report a previously unknown pattern of cell wall for mation in the tracheids of a living plant. We show that in Huperzia, one of the most primitive extant vascular plants, secondary cell wall deposition in tracheids includes a first-formed layer of wall material that is degrada tion-prone ("template layer") and a later-formed degradation-resistant laye r ("resistant layer"). These layers match precisely the pattern of wall thi ckenings in the tracheids of early fossil vascular plants and provide an ev olutionary link between tracheids of living vascular plants and those of th eir earliest fossil ancestors. Moreover, our developmental data provide the essential information for an explicit model of the early evolution of trac heid secondary wall thickenings. Finally, congruence of tracheid structure in extant Huperzia and Late Silurian and Early Devonian vascular plants sup ports the hypothesis of a single origin of tracheids in land plants.