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Colonization of terrestrial ecosystems by the first land plants, and their subsequent expansion and diversification, were crucial for the life on the Earth. However, our understanding of these processes is still relatively poor. Recent intensification of studies on various plant organisms have identified the plant cell walls are those structures, which played a key role in adaptive processes during the evolution of land plants. Cell wall as a structure protecting protoplasts and showing a high structural plasticity was one of the primary subjects to changes, giving plants the new properties and capabilities, which undoubtedly contributed to the evolutionary success of land plants. In this paper, the current state of knowledge about some main components of the cell walls (cellulose, hemicelluloses, pectins and lignins) and their evolutionary alterations, as preadaptive features for the land colonization and the plant taxa diversification, is summarized. Some aspects related to the biosynthesis and modification of the cell wall components, with particular emphasis on the mechanism of transglycosylation, are also discussed. In addition, new surprising discoveries related to the composition of various cell walls, which change how we perceive their evolution, are presented, such as the presence of lignin in red algae or MLG (1→3),(1→4)-β-D-glucan in horsetails. Currently, several new and promising projects, regarding the cell wall, have started, deciphering its structure, composition and metabolism in the evolutionary context. That additional information will allow us to better understand the processes leading to the terrestrialization and the evolution of extant land plants.
Axial homodromy in growing shoots of perennial plants with spiral phyllotaxis is the case when the chirality of phyllotactic pattern does not change in consecutive growth increments of the same axis. In conifers such as Picea or Abies this rule is strictly observed, except for the rare cases of discontinuous phyllotactic transitions. In Torreya, however, the chirality changes, at random, every year. The pattern of primordia packing, executed by vegetative shoot apical meristem (SAM), depends in Torreya on their identity. The primordia of bud scales are initiated in the decussate and those of needles in bijugate spiral pattern. The decussate, achiral i.e. neutral pattern always precedes the formation of new spiral pattern and thus facilitates random selection of its chiral configuration. Periodic change in organ identity cannot itself be responsible for the special behavior of Torreya, because in other conifers it also exists. There is, however, one important difference: in Torreya, when the initiation of bud scales begins at SAM, the distance between differentiated protoxylem and the initiation site gradually increases, while in other conifers it remains constant and small. In Torreya, at this phase of development, the rate of xylem differentiation and the rate of organogenesis become uncoupled. Closer anatomical examination shows that the decussate pattern in a bud scale zone develops slowly suggesting gradual decrease of the putative signal flowing acropetally from differentiated protoxylem, responsible for positioning of primordia. We hypothesize that in the absence of this signal SAM starts acting autonomously, distributing primordia according to their identity only. A constant presence of the signal in other conifers assures the continuation of the same phyllotactic pattern throughout the period of bud scale formation, despite the change in organ identity.
Regularity and periodicity in the arrangements of organs in all groups of land plants raise questions about the mechanisms underlying phyllotactic pattern formation. The initiation of the lateral organs (leaves, flowers, etc.), and thus, their spatio-temporal positioning, occurs in the shoot apical meristem (SAM) and is related to the structure and organogenic activity of the meristem. In this review, we present some aspects of the diversity and stability of phyllotactic patterns in the major lineages of land plants, from bryophytes to angiosperms, in which SAM structures differ significantly. In addition, we discuss some of the possible mechanisms involved in the formation of the recurring arrangement of the lateral organs.
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