Literature DB >> 24311086

Water permeability of Betula periderm.

J Schönherr1, H Ziegler.   

Abstract

The water permeability of periderm membranes stripped from mature trees of Betula pendula Roth was investigated. The diffusion of water was studied using the system water/membrane/water, and transpiration was measured using the system water/membrane/water vapor. Betula periderm consists of successive periderm layers each made up of about 5 heavily suberized cell layers and a varying number of cell layers that are little suberized, if at all. It is shown that these layers act as resistances in series. The permeability coefficient of the diffusion of water (P d) can be predicted with 79% accuracy from the reciprocal of the membrane weight (x in mg cm(-2)) by means of the linear equation P d=14.69·10(-7) x-0.73·10(-7). For example, the P d of a periderm membrane having a weight of 10 mg cm(-2) (approx. 250 μm thick) is 7.4·10(-8) cm s(-1), which is comparable to the permeability of cuticles. This comparison shows that on a basis of unit thickness, Betula periderm is quite permeable to water as cuticles have the same resistance with a thickness of only 0.5 to 3 μm. It is argued that this comparatively high water permeability of birch periderm is due to the fact that middle lamellae and the primary walls of periderm cells are not at all, or only incompletely suberized and, therefore, form a hydrophilic network within which the water can flow. This conclusion is based on the following observations: (1) Middle lamellae and primary walls stain strongly with toluidine blue, which shows them to be polar. (2) If silver ions are added as tracer for the flow of water, they are found only in the middle lamellae, primary walls, and in plasmodesmata, while no silver can be detected in the suberized walls. (3) Permeability coefficients of transpiration strongly depend on water activity. This shows conclusively that water flows across Betula periderm via a polar pathway. It is further argued that liquid continuity is likely to be maintained under all physiological conditions in the network formed by middle lamellae and primary walls. On the other hand, the lumina of periderm cells, intercellular air spaces in the lenticels, and even the pores in the suberized walls (remainders of plasmodesmata) will drain at a humidity of 95% and below. Due to the presence of intercellulars the permeability coefficient of lenticels is much greater than that of the periderm. A substantial amount of the total water, therefore, flows as vapor through lenticels even though they cover only 3% of the surface.

Entities:  

Year:  1980        PMID: 24311086     DOI: 10.1007/BF00379844

Source DB:  PubMed          Journal:  Planta        ISSN: 0032-0935            Impact factor:   4.116


  7 in total

1.  [Minute construction of corked up cell walls].

Authors:  P SITTE
Journal:  Mikroskopie       Date:  1955-12

2.  Water permeability of plant cuticles : Dependence of permeability coefficients of cuticular transpiration on vapor pressure saturation deficit.

Authors:  J Schönherr; H W Schmidt
Journal:  Planta       Date:  1979-01       Impact factor: 4.116

3.  A low-viscosity epoxy resin embedding medium for electron microscopy.

Authors:  A R Spurr
Journal:  J Ultrastruct Res       Date:  1969-01

4.  Water permeability of plant cuticles: The effect of temperature on diffusion of water.

Authors:  J Schönherr; K Eckl; H Gruler
Journal:  Planta       Date:  1979-10       Impact factor: 4.116

5.  Composition of soluble cuticular lipids and water permeability of cuticular membranes from Citrus leaves.

Authors:  K Haas; J Schönherr
Journal:  Planta       Date:  1979-09       Impact factor: 4.116

6.  Biochemistry of Suberization: Incorporation of [1-C]Oleic Acid and [1-C]Acetate into the Aliphatic Components of Suberin in Potato Tuber Disks (Solanum tuberosum).

Authors:  B B Dean; P E Kolattukudy
Journal:  Plant Physiol       Date:  1977-01       Impact factor: 8.340

7.  Water permeability of isolated cuticular membranes: The effect of pH and cations on diffusion, hydrodynamic permeability and size of polar pores in the cutin matrix.

Authors:  J Schönherr
Journal:  Planta       Date:  1976-01       Impact factor: 4.116

  7 in total
  11 in total

1.  Evidence for active cyclic electron flow in twig chlorenchyma in the presence of an extremely deficient linear electron transport activity.

Authors:  Ch Kotakis; Y Petropoulou; K Stamatakis; Ch Yiotis; Y Manetas
Journal:  Planta       Date:  2006-06-14       Impact factor: 4.116

2.  Casparian bands occur in the periderm of Pelargonium hortorum stem and root.

Authors:  Chris J Meyer; Carol A Peterson
Journal:  Ann Bot       Date:  2011-01-14       Impact factor: 4.357

3.  Winter peridermal conductance of apple trees: lammas shoots and spring shoots compared.

Authors:  B Beikircher; S Mayr
Journal:  Trees (Berl West)       Date:  2012-12-14       Impact factor: 2.529

4.  Physiological characterization of the wild almond Prunus arabica stem photosynthetic capability.

Authors:  Taly Trainin; Hillel Brukental; Or Shapira; Ziv Attia; Vivekanand Tiwari; Kamel Hatib; Shira Gal; Hanita Zemach; Eduard Belausov; Dana Charuvi; Doron Holland; Tamar Azoulay-Shemer
Journal:  Front Plant Sci       Date:  2022-07-29       Impact factor: 6.627

5.  A central role of abscisic acid in drought stress protection of Agrobacterium-induced tumors on Arabidopsis.

Authors:  Marina Efetova; Jürgen Zeier; Markus Riederer; Chil-Woo Lee; Nadja Stingl; Martin Mueller; Wolfram Hartung; Rainer Hedrich; Rosalia Deeken
Journal:  Plant Physiol       Date:  2007-09-07       Impact factor: 8.340

6.  Wax and suberin development of native and wound periderm of potato (Solanum tuberosum L.) and its relation to peridermal transpiration.

Authors:  Lukas Schreiber; Rochus Franke; Klaus Hartmann
Journal:  Planta       Date:  2004-09-17       Impact factor: 4.116

7.  Water permeability of periderm membranes isolated enzymatically from potato tubers (Solanum tuberosum L.).

Authors:  E Vogt; J Schönherr; H W Schmidt
Journal:  Planta       Date:  1983-08       Impact factor: 4.116

8.  Composition, ultrastructure and function of the cutin- and suberin-containing layers in the leaf, fruit peel, juice-sac and inner seed coat of grapefruit (Citrus paradisi Macfed.).

Authors:  K E Espelie; R W Davis; P E Kolattukudy
Journal:  Planta       Date:  1980-10       Impact factor: 4.116

9.  The Arabidopsis cytochrome P450 CYP86A1 encodes a fatty acid omega-hydroxylase involved in suberin monomer biosynthesis.

Authors:  Rene Höfer; Isabel Briesen; Martina Beck; Franck Pinot; Lukas Schreiber; Rochus Franke
Journal:  J Exp Bot       Date:  2008       Impact factor: 6.992

10.  Hypoxia in grape berries: the role of seed respiration and lenticels on the berry pedicel and the possible link to cell death.

Authors:  Zeyu Xiao; Suzy Y Rogiers; Victor O Sadras; Stephen D Tyerman
Journal:  J Exp Bot       Date:  2018-04-09       Impact factor: 6.992

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