Hostname: page-component-84b7d79bbc-g7rbq Total loading time: 0 Render date: 2024-07-28T04:43:04.375Z Has data issue: false hasContentIssue false

Water relations and xylem anatomy of ferns

Published online by Cambridge University Press:  05 December 2011

A. C. Gibson
Affiliation:
Department of Biology and Laboratory of Biomedical and Environmental Sciences, University of California, Los Angeles, California 90024, U.S.A.
H. W. Calkin
Affiliation:
Department of Biology and Laboratory of Biomedical and Environmental Sciences, University of California, Los Angeles, California 90024, U.S.A.
D. O. Raphael
Affiliation:
Department of Biology and Laboratory of Biomedical and Environmental Sciences, University of California, Los Angeles, California 90024, U.S.A.
P. S. Nobel
Affiliation:
Department of Biology and Laboratory of Biomedical and Environmental Sciences, University of California, Los Angeles, California 90024, U.S.A.
Get access

Synopsis

The entire soil-plant-atmosphere continuum must be analysed to elucidate how xylem anatomy relates to water flow in plants. Measurements of water potential gradients and volume of water flow per unit time are needed to obtain values of hydraulic conductance per unit length. By comparing values of hydraulic conductance per unit length along the plant, the regions where xylem structure restricts water flow can be determined. Previous studies of fern water relations demonstrated that very large water potential gradients occurring in stipes of certain ferns were closely correlated with reduced conducting area of stipe xylem. A new study on Cyrtomium falcatum showed that the water potential gradient was relatively small and constant along the stipe and rachis; however, a much larger gradient occurred from the rachies into the pinnae. Hydraulic conductance per unit length varied with the leaf area to be supplied, leading to the fairly constant water potential gradient along the rachis.. The measured hydraulic conductance per unit length was only half the value predicted from the Hagen-Poiseuille equation. Although the Hagen-Poiseuille equation overestimated the measured value by a factor of 2, it did support the assumption that conduit number and lumen diameter are the principal determinants of water conductance in the xylem.

Type
Research Article
Copyright
Copyright © Royal Society of Edinburgh 1985

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

Beck, C. B., Schmid, R. and Rothwell, G. W. 1982. Stelar morphology and the primary vascular system of seed plants. Bot. Rev. 48, 691815.CrossRefGoogle Scholar
Bierhorst, D. W. 1971. Morphology of vascular plants. New York: Macmillan.Google Scholar
Bower, F. O. 1935. Primitive land plants. London: Macmillan.Google Scholar
Dimond, A. E. 1966. Pressure and flow relations in vascular bundles of the tomato plant. Pl. Physiol. 41, 119131.CrossRefGoogle ScholarPubMed
Gibson, A. C., Calkin, H. W. and Nobel, P. S. 1984. Xylem anatomy, water flow, and hydraulic conductance in the fern Cyrtomium falcatum. Am. J. Bot. 71, 564574.CrossRefGoogle Scholar
Giordano, R., Salleo, A., Salleo, S. and Wanderlingh, F. 1978. Flow in xylem vessels and Poiseuille's Law. Can. J. Bot. 56, 333338.CrossRefGoogle Scholar
Hinckley, T. M., Lassoie, J. P. and Running, S. W. 1978. Temporal and spatial variations in the water status of forest trees. U.S. Forest Serv. Monogr. 20. Washington D.C.Google Scholar
Huber, B. and Schmidt, E. 1936. Weitere thermo-elektrische Untersuchungen uber den Transpirationsstrom der Baume. Tharandt. Forstl. Jb. 87, 369412.Google Scholar
Huber, B. and Schmidt, E. 1937. Eine Kompensationsmethode zur thermo-elektrischen Messung langsamer Saftstrome. Ber. Dt. Bot. Ges. 55, 514529.Google Scholar
Jeje, A. A. and Zimmermann, M. H. 1979. Resistance to water flow in xylem vessels. J. Exp. Bot. 30, 817827.CrossRefGoogle Scholar
Murray, B. J., Mauk, C. and Nooden, L. D. 1982. Restricted vascular pipelines (and orthostichies) in plants. What's New in Plant Physiology 13, 3336.Google Scholar
Nobel, P. S. 1977. Internal leaf area and cellular CO2 resistance: photosynthetic implications of variations with growth conditions and plant species. Physiologia Pl. 40, 137144.CrossRefGoogle Scholar
Nobel, P. S. 1978. Microhabitat, water relations, and photosynthesis of a desert fern, Notholaena parryi. Oecologia 31, 293309.CrossRefGoogle ScholarPubMed
Nobel, P. S. 1983. Biophysical plant physiology and ecology. San Francisco/New York: W. H. Freeman.Google Scholar
Ogura, Y. 1972. Comparative anatomy of vegetative organs of the pteridophytes. Handbuch der Pflanzenanatomie 7 (3). Berlin: Gebrüder Borntraeger.Google Scholar
Roach, W. A. 1939. Plant injection as a physiological method. Ann. Bot. 3, 155226.CrossRefGoogle Scholar
Scholander, P. F., Hammel, H. T., Bradstreet, E. D. and Hemmingsen, E. A. 1965. Sap pressure in vascular plants. Science, N.Y. 148, 339346.CrossRefGoogle ScholarPubMed
Tyree, M. T. and Zimmermann, M. H. 1971. The theory and practice of measuring transport coefficients and sap flow in the xylem of red maple stems (Acer rubrum). J. Exp. Bot. 22, 118.CrossRefGoogle Scholar
Woodhouse, R. M. and Nobel, P. S. 1982. Stipe anatomy, water potentials, and xylem conductances in seven species of ferns (Filicopsida). Am. J. Bot. 69, 135140.CrossRefGoogle Scholar
Zimmermann, M. H. 1971. Transport in the xylem. In Trees. Structure and function, ed. Zimmermann, M. H. and Brown, C. L., pp. 169220. New York: Springer.Google Scholar
Zimmermann, M. H. 1983. Xylem structure and the ascent of sap. New York: Springer.CrossRefGoogle Scholar