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Primary Xylem (primary + xylem)
Selected AbstractsThe spatial pattern of air seeding thresholds in mature sugar maple treesPLANT CELL & ENVIRONMENT, Issue 9 2005BRENDAN CHOAT ABSTRACT Air seeding threshold (Pa) of xylem vessels from current year growth rings were measured along the vertical axis of mature sugar maple trees (Acer saccharum Marsh.), with sampling points in primary leaf veins, petioles, 1-, 3-, and 7-year-old branches, large branches, the trunk and roots. The air seeding threshold was taken as the pressure required to force nitrogen gas through intervessel pit membranes. Although all measurements were made on wood produced in the same year, Pa varied between different regions of A. saccharum, with distal organs such as leaves and petioles having lower Pa than basal regions. Mean (SE) Pa ranged from 1.0 (± 0.1) MPa in primary leaf veins to 4.8 (± 0.1) MPa in the main trunk. Roots exhibited a Pa of 2.8 (± 0.2) MPa, lower than all other regions of the tree except leaf veins and petioles. Mean xylem vessel diameter increased basipetally, with the widest vessels occurring in the trunk and roots. Within the shoot, wider vessels had greater air seeding thresholds, contrasting with trends previously reported. However, further experimentation revealed that differences in Pa between regions of the stem were driven by the presence of primary xylem conduits, rather than differences in vessel diameter. In 1-year-old branches, Pa was significantly lower in primary xylem vessels than in adjacent secondary xylem vessels. This explained the lower values of Pa measured in petioles and leaf veins, which possessed a greater ratio of primary xylem to secondary xylem than other regions. The difference in Pa between primary and secondary xylem was attributed to the greater area of primary cell wall (pit membrane) exposed in primary xylem conduits with helical or annular thickening. [source] Xylem heterochrony: an unappreciated key to angiosperm origin and diversificationsBOTANICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 1 2009SHERWIN CARLQUIST fls All angiosperms can be arranged along a spectrum from a preponderance of juvenile traits (cambial activity lost) to one of nearly all adult characters (cambium maximally active, mature patterns realized rapidly early in ontogeny). Angiosperms are unique among seed plants in the width of this spectrum. Xylem patterns are considered here to be indicative of contemporary function, not relictual. Nevertheless, most families of early-divergent angiosperms exhibit paedomorphic xylem structure, a circumstance that is most plausibly explained by the concept that early angiosperms had sympodial growth forms featuring limited accumulation of secondary xylem. Sympodial habits have been retained in various ways not only in early-divergent angiosperms, but also among eudicots in Ranunculales. The early angiosperm vessel, relatively marginal in conductive abilities, was improved in various ways, with concurrent redesign of parenchyma and fibre systems to enhance conductive, storage and mechanical capabilities. Flexibility in degree of cambial activity and kinds of juvenile/adult expressions has been basic to diversification in eudicots as a whole. Sympodial growth that lacks cambium, such as in monocots, provides advantages by various features, such as organographic compartmentalization of tracheid and vessel types. Woody monopodial eudicots were able to diversify as a result of production of new solutions to embolism prevention and conductive efficiency, particularly in vessel design, but also in parenchyma histology. Criteria for paedomorphosis in wood include slow decrease in length of fusiform cambial initials, predominance of procumbent ray cells and lesser degrees of cambial activity. Retention of ancestral features in primary xylem (the ,refugium' effect) is, in effect, a sort of inverse evidence of acceleration of adult patterns in later formed xylem. Xylem heterochrony is analysed not only for all key groups of angiosperms (including monocots), but also for different growth forms, such as lianas, annuals, various types of perennials, rosette trees and stem succulents. Xylary phenomena that potentially could be confused with heterochrony are discussed. Heterochronous xylem features seem at least as important as other often cited factors (pollination biology) because various degrees of paedomorphic xylem are found in so many growth forms that relate in xylary terms to ecological sites. Xylem heterochrony can probably be accessed during evolution by relatively simple gene changes in a wide range of angiosperms and thus represents a current as well as a past source of variation upon which diversification was based. Results discussed here are compatible with both current molecular-based phylogenetic analyses and all recent physiological work on conduction in xylem and thus represent an integration of these fields. © 2009 The Linnean Society of London, Botanical Journal of the Linnean Society, 2009, 161, 26,65. [source] Radial secondary growth and formation of successive cambia and their products in Ipomoea hederifolia L. (Convolvulaceae)BOTANICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 1 2008KISHORE S. RAJPUT Ipomoea hederifolia stems increase in thickness using a combination of different types of cambial variant, such as the discontinuous concentric rings of cambia, the development of included phloem, the reverse orientation of discontinuous cambial segments, the internal phloem, the formation of secondary xylem and phloem from the internal cambium, and differentiation of cork in the pith. After primary growth, the first ring of cambium arises between the external primary phloem and primary xylem, producing secondary phloem centrifugally and secondary xylem centripetally. The stem becomes lobed, flat, undulating, or irregular in shape as a result of the formation of both discontinuous and continuous concentric rings of cambia. As the formation of secondary xylem is greater in one region than in another, this results in the formation of a grooved stem. Successive cambia formed after the first ring are of two distinct functional types: (1) functionally normal successive cambia that divide to form secondary xylem centripetally and secondary phloem centrifugally, like other dicotyledons that show successive rings, and (2) abnormal cambia with reverse orientation. The former type of successive rings originates from the parenchyma cells located outside the phloem produced by previous cambium. The latter type of cambium develops from the conjunctive tissue located at the base of the secondary xylem formed by functionally normal cambia. This cambium is functionally inverted, producing secondary xylem centrifugally and secondary phloem centripetally. In later secondary growth, xylem parenchyma situated deep inside the secondary xylem undergoes de-differentiation, and re-differentiates into included phloem islands in secondary xylem. © 2008 The Linnean Society of London, Botanical Journal of the Linnean Society, 2008, 158, 30,40. [source] Rotafolia songziensis gen. et comb. nov., a sphenopsid from the Late Devonian of Hubei, ChinaBOTANICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 1 2005DE-MING WANG A sphenopsid from the Upper Devonian (Famennian) Xiejingsi Formation, south-western Hubei Province, China, previously named as various species in Sphenophyllum, Hamatophyton, Bowmanites and Sphenophyllostachys, is now reinvestigated and assigned to a new taxon, Rotafolia songziensis gen. et comb. nov. Its ribbed axes are anisotomous and possess slightly expanded nodes. Lateral axes are inserted at nodes on main axes. Whorls of much divided vegetative leaves are attached at nearly right angles to nodes of basal axes, and at acute angles to nodes of terminal axes. There are six leaves per whorl. The terminal strobilus includes a central axis and verticils of fertile units. Each fertile unit consists of a bract and numerous sporangia. The margin of the elongate-cuneate bract bears a distal and many lateral elongate segments. Clusters of elongate sporangia are abaxially attached to the base of the bract at the same level. The axis has an actinostele, composed of a three-ribbed, exarch primary xylem and radial secondary xylem. Although Rotafolia songziensis closely resembles Hamatophyton verticillatum in axis character, leaf morphology and primary xylem type, they are quite different in strobilar structure. Taxonomically, Rotafolia is placed in the order Sphenophyllales by three well-defined characters: 1) whorled appendages; 2) ribbed protosteles; 3) exarch primary xylem maturation. © 2005 The Linnean Society of London, Botanical Journal of the Linnean Society, 2005, 148, 21,37. [source] Hamatophyton from the Late Devonian of Anhui Province, South China and Evolution of SphenophyllalesACTA GEOLOGICA SINICA (ENGLISH EDITION), Issue 3 2009Deming WANG Abstract: Well-preserved specimens of Hamatophyton verticillatum collected from the Upper Devonian (Famennian) Wutong Formation of Chaohu district, Anhui Province, South China, display more complete fertile axes in three orders and multiple divisions. Comparisons indicate that Hamatophyton possibly does not have palmate planate sterile leaves but hook-like linear ones with rare divisions. We propose seven definitive characters of Sphenophyllales: (1) completely whorled lateral organs; (2) sterile leaves; (3) strobili; (4) "sporangiophores" or stalks with reflexed tips bearing sporangia; (5) three- or four-ribbed primary xylem; (6) exarch maturation of primary xylem; and (7) secondary xylem. The Sphenophyllales probably originated from the Iridopteridales based on similarities in whorled lateral organs, ribbed primary xylem and peripheral protoxylem strands. In transition from Iridopteridales to Sphenophyllales, morphological changes involve partially whorled to completely whorled lateral organs, sterile ultimate appendages to leaves, and fertile ultimate appendages to "sporangiophores"/stalks with bracts; anatomical modifications include configuration and maturation of primary xylem, and presence of secondary xylem. [source] | ||||||||||