Hostname: page-component-5c6d5d7d68-tdptf Total loading time: 0 Render date: 2024-08-21T05:19:07.413Z Has data issue: false hasContentIssue false

A physical model involving Nuclepore membranes to investigate the mechanism of humidity-induced convection in Phragmites australis

Published online by Cambridge University Press:  05 December 2011

J. Armstrong
Affiliation:
Dept. of Applied Biology, University of Hull, Kingston upon Hull, HU6 7RX, UK
W. Armstrong
Affiliation:
Dept. of Applied Biology, University of Hull, Kingston upon Hull, HU6 7RX, UK
Get access

Synopsis

Nuclepore membranes of known pore size and porosity, attached to small glass chambers were used to investigate the mechanism of humidity-induced convection found in Phragmites and other species. The convective flow of gases and the development of static pressures were studied in relation to a variety of conditions imposed on opposite sides of the membrane. Data were obtained in relation to pore size (0.015 to 3 μm diameter) and porosity, temperature and humidity gradients, membrane area and resistance to venting.

A humidity gradient across the Nuclepore membranes was far more effective than a temperature gradient per se for inducing flow; also pores of the order 0.2 μm diameter were the most effective. With a steep enough humidity gradient, however, significant flows could also be induced across pores as large as 2 μm diameter. The results accord with previous experiments and observations on Phragmites and with the mathematical treatment of the mechanism. It is concluded that humidity-induced convection should play a greater role than thermal transpiration (thermo-osmosis) in effecting convections in Phragmites and other non-floating-leaved species.

Type
Research Article
Copyright
Copyright © Royal Society of Edinburgh 1994

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Armstrong, J. & Armstrong, W. 1990a. Light enhanced convective throughflow increases oxygenation in rhizomes and rhizosphere of Phragmites australis (Cav.) Trin. ex Steud. New Phytologist 114, 121–8.CrossRefGoogle ScholarPubMed
Armstrong, J. & Armstrong, W. 1990b. Pathways and mechanisms of oxygen transport in Phragmites australis. In Cooper, P. F. & Findlater, B. C. (Eds) The use of constructed wetlands in water pollution control, pp. 529–33. Oxford: Pergamon Press.CrossRefGoogle Scholar
Armstrong, J. & Armstrong, W. 1991. A convective throughflow of gases in Phragmites australis. Aquatic Botany 39, 7588.CrossRefGoogle Scholar
Armstrong, J. 1992. Pathways and mechanisms of aeration in Phragmites australis. University of Hull: Ph.D. Thesis.Google Scholar
Armstrong, J., Armstrong, W. & Beckett, P. M. 1988. Phragmites australis: a critical appraisal of the ventilating pressure concept and an analysis of resistance to pressurized gas flow and gaseous diffusion in horizontal rhizomes. New Phytologist 110, 383389.CrossRefGoogle Scholar
Armstrong, J., Armstrong, W. & Beckett, P. M. 1992. Phragmites australis: Venturi- and humidity-induced convections enhance rhizome aeration and rhizosphere oxidation. New Phytologist 120, 197207.CrossRefGoogle Scholar
Armstrong, W., Armstrong, J., Beckett, P. M. & Justin, S. H. F. W. 1990. Convective gas-flows in wetland plant aeration. In Jackson, M. B., Davies, D. D. & Lambers, H. (Eds) Plant life under oxygen stress pp. 283302, The Hague: SPB Academic Publishing bv.Google Scholar
Brix, H. 1988. Light dependent variation in the composition of the internal atmosphere of Phragmites australis (Cav.) Trin. ex. Steud. Aquatic Botany 30, 319–29.CrossRefGoogle Scholar
Brix, H., Sorrell, B. K. & Orr, P. T. 1992. Internal pressurization and convective gas flow in some emergent freshwater macrophytes. Limnology & Oceanography 37, 1420–33.CrossRefGoogle Scholar
Dacey, J. W. H. 1981. Pressurised ventilation in the yellow water-lily. Ecology 62, 1137–47.CrossRefGoogle Scholar
Dacey, J. W. A. 1987. Knudsen-transitional flow and gas pressurisation in leaves of Nelumbo. Plant Physiology 85, 199203.CrossRefGoogle ScholarPubMed
Egginton, S. & Ross, H. F. (Eds). 1992. Oxygen transport in biological systems: Modelling of pathways from environment to cell. SEB Seminar Series, 51. Cambridge: Cambridge University Press, 298 pages.Google Scholar
Grosse, W. & Bauch, C. 1991. Gas transfer in floating-leaved plants. Vegetatio 97, 185–92.CrossRefGoogle Scholar
Grosse, W. & Buchel, H. B. & Tiébel, H. 1991. Pressurized ventilation in wetland plants. Aquatic Botany 39, 8998.CrossRefGoogle Scholar
Reynolds, O. 1879. On certain dimensional properties of matter in the gaseous state. Philosophy Transactions 170, 727845.Google Scholar
Schroder, P., Grosse, W. & Woermann, D. 1986. Localisation of thermo-osmotically active partitions in young leaves of Nuphar lutea. Journal of Experimental Botany 37, 1450–61.CrossRefGoogle Scholar