Pit Membrane Porosity and Water Stress-Induced Cavitation in Four Co-Existing Dry Rainforest Tree Species

Aspects of xylem anatomy and vulnerability to water stress-induced embolism were examined in stems of two drought-deciduous species, Brachychiton australis (Schott and Endl.) A. Terracc. and Cochlospermum gillivraei Benth., and two evergreen species, Alphitonia excelsa (Fenzal) Benth. and Austromyrtus bidwillii (Benth.) Burret., growing in a seasonally dry rainforest. The deciduous species were more vulnerable to water stress-induced xylem embolism. B. australis andC. gillivraei reached a 50% loss of hydraulic conductivity at −3.17 MPa and −1.44 MPa, respectively; a 50% loss of hydraulic conductivity occurred at −5.56 MPa in A. excelsa and −5.12 MPa in A. bidwillii. To determine whether pit membrane porosity was responsible for greater vulnerability to embolism (air seeding hypothesis), pit membrane structure was examined. Expected pore sizes were calculated from vulnerability curves; however, the predicted inter-specific variation in pore sizes was not detected using scanning electron microscopy (pores were not visible to a resolution of 20 nm). Suspensions of colloidal gold particles were then perfused through branch sections. These experiments indicated that pit membrane pores were between 5 and 20 nm in diameter in all four species. The results may be explained by three possibilities: (a) the pores of the expected size range were not present, (b) larger pores, within the size range to cause air seeding, were present but were rare enough to avoid detection, or (c) pore sizes in the expected range only develop while the membrane is under mechanical stress (during air seeding) due to stretching/flexing.

[1]  The fine structure of the pits of Eucalyptus regnans (F. Muell.) and their relation to the movement of liquids into the wood. , 1960 .

[2]  W. Pickard The ascent of sap in plants , 1981 .

[3]  M. Zimmermann,et al.  Vessel-length distribution in stems of some American woody plants , 1981 .

[4]  B. Meylan,et al.  Cell wall hydrolysis in the tracheary elements of the secondary xylem , 1982 .

[5]  M. Zimmermann Xylem Structure and the Ascent of Sap , 1983, Springer Series in Wood Science.

[6]  N. V. Van Alfen,et al.  Role of pit membranes in macromolecule-induced wilt of plants. , 1983, Plant physiology.

[7]  M. Hipkins,et al.  Gas penetration of pit membranes in the xylem of Rhododendron as the cause of acoustically detectable sap cavitation , 1985 .

[8]  J. Sperry,et al.  Mechanism of water stress-induced xylem embolism. , 1988, Plant physiology.

[9]  A. M. Lewis,et al.  A test of the air-seeding hypothesis using sphagnum hyalocysts. , 1988, Plant physiology.

[10]  A. Tyree,et al.  Vulnerability of Xylem to Cavitation and Embolism , 1989 .

[11]  J. Sperry,et al.  Pit Membrane Degradation and Air-Embolism Formation in Ageing Xylem Vessels of Populus tremuloides Michx , 1991 .

[12]  M. Tyree,et al.  Use of positive pressures to establish vulnerability curves : further support for the air-seeding hypothesis and implications for pressure-volume analysis. , 1992, Plant physiology.

[13]  J. Milburn Water Transport in Plants under Climatic Stress: Cavitation. A review: past, present and future , 1993 .

[14]  John S. Sperry,et al.  Intra‐ and inter‐plant variation in xylem cavitation in Betula occidentalis , 1994 .

[15]  S. Davis,et al.  Biophysical Perspectives of Xylem Evolution: is there a Tradeoff of Hydraulic Efficiency for Vulnerability to Dysfunction? , 1994 .

[16]  J. A. Jarbeau,et al.  The mechanism of water‐stress‐induced embolism in two species of chaparral shrubs , 1995 .

[17]  R. van den Driessche,et al.  Nutrition, xylem cavitation and drought resistance in hybrid poplar. , 1997, Tree physiology.

[18]  C. V. Willigen,et al.  A mathematical and statistical analysis of the curves illustrating vulnerability of xylem to cavitation. , 1998, Tree physiology.

[19]  M. Mccully,et al.  Architecture of Branch-root Junctions in Maize: Structure of the Connecting Xylem and the Porosity of Pit Membranes , 2000 .

[20]  W. Dickison,et al.  Integrative Plant Anatomy , 2000 .

[21]  G Goldstein,et al.  Water transport in trees: current perspectives, new insights and some controversies. , 2001, Environmental and experimental botany.

[22]  J. Sperry,et al.  Cavitation fatigue. Embolism and refilling cycles can weaken the cavitation resistance of xylem. , 2001, Plant physiology.

[23]  J. Sperry,et al.  Cavitation fatigue and its reversal in sunflower (Helianthus annuus L.). , 2002, Journal of experimental botany.

[24]  J. Sperry,et al.  Root and stem xylem embolism, stomatal conductance, and leaf turgor in Acer grandidentatum populations along a soil moisture gradient , 1996, Oecologia.

[25]  R. Machado,et al.  Pit membranes in hardwoods—Fine structure and development , 1968, Protoplasma.