Oxygen distribution in wetland plant roots and permeability barriers to gas-exchange with the rhizosphere: a microelectrode and modelling study with Phragmites australis

Citation
W. Armstrong et al., Oxygen distribution in wetland plant roots and permeability barriers to gas-exchange with the rhizosphere: a microelectrode and modelling study with Phragmites australis, ANN BOTANY, 86(3), 2000, pp. 687-703
Citations number
51
Categorie Soggetti
Plant Sciences
Journal title
ANNALS OF BOTANY
ISSN journal
03057364 → ACNP
Volume
86
Issue
3
Year of publication
2000
Pages
687 - 703
Database
ISI
SICI code
0305-7364(200009)86:3<687:ODIWPR>2.0.ZU;2-K
Abstract
Adventitious roots of intact Phragmites plantlets were secured horizontally 2-3 mm below the surface of an oxygen-depleted fluid agar across which oxy gen-free nitrogen was gently streamed to create a constant oxygen sink; the leafy shoot was fully exposed to air. Radial oxygen profiles through rhizo sphere and root at different distances from the apex were obtained polarogr aphically using Clark-type bevelled microelectrodes servo-driven in steps o f 10 mu m (root) or 10-50 mu m (rhizosphere). The pattern of radial oxygen loss (ROL) typical of wetland plants, viz. high at the apex and declining s harply sub-apically, was related to synergism between ROL, and oxygen consu mption and increasing impedance to diffusion within the epidermal/hypoderma l cylinder rather than to a surface resistance. The smallest oxygen deficit (2 kPa) to develop across the 80 mu m thick epidermal/hypodermal cylinder was within the apical 10 mm and was consistent with tissue oxygen diffusivi ties similar to water. At 100 mm from the apex, consumption and impedance h ad increased the deficit to about 15 kPa and reduced ROL almost to zero. Th e developing impedance within the epidermal/hypodermal cylinder was least i n cell layers immediately adjoining the cortex and increased most in the hy podermal cell layer abutting the epidermis. The sub-apical decline in ROL a ppeared to coincide with the appearance of aerenchyma in the cortex but thi n walled 'passage areas' (windows) in the hypodermal/epidermal cylinder per sisted locally and remained leaky to oxygen to some degree. It is through t hese windows that lateral roots emerge and the cortex in line with the wind ows remains non-aerenchymatous. The radial and longitudinal oxygen profiles were consistent with modelling predictions. The shapes of the stelar oxyge n profiles were consistent with a higher oxygen demand in the outer region (viz. pericycle, phloem, protoxylem and early metaxylem cylinder) than in t he inner core (late metaxylem cylinder and medulla), but the deficits were relatively small (less than or equal to 3 kPa) and consistent with minimal wall thickening in the endodermis and narrowness of stele. The possible rel evance of the results to entry of methane and other products from the rhizo sphere into root and to the mechanism of aerenchyma formation are discussed . (C) 2000 Annals of Botany Company.