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Dimensions and distribution of intercellular spaces in cryo‐planed soybean nodules
Author(s) -
Cauwenberghe Owen R.,
Newcomb William,
Canny Martin J.,
Layzell David B.
Publication year - 1993
Publication title -
physiologia plantarum
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.351
H-Index - 146
eISSN - 1399-3054
pISSN - 0031-9317
DOI - 10.1111/j.1399-3054.1993.tb00151.x
Subject(s) - intracellular , scanning electron microscope , diffusion , permeability (electromagnetism) , gaseous diffusion , biophysics , chemistry , materials science , biology , composite material , physics , biochemistry , electrode , membrane , thermodynamics
The ability of legume nodules to regulate their permeability to gas diffusion has been attributed to physiological control over the size and distribution of gas‐filed intercellular spaces within the nodule cortex. To examine the size and distribution of intercellular spaces and to determine whether they were filled with gas (high diffusion permeability) or liquid (low diffusion permeability), whole nodules were frozen in liquid nitrogen slush (‐210°C), and then either cryo‐fractured or cryo‐planed before being examined by cold‐stage scanning electron microscopy (SEM). The cryo‐planed tissue was found to have many advantages over cryo‐fractured nodules in providing images which were easier to interpret and quantify. Intercellular spaces throughout the nodule were examined in both tangential and medial planed faces. Since no differences were observed between views in either the size or shape of the open intercellular spaces, it was concluded that the intercellular spaces of nodules were not radially oriented as assumed in many mathematical models of gas diffusion. The inner cortex region in the nodules had the smallest intercellular spaces compared to other zones, and less than 10% of the intercellular spaces were occluded with any type of material in the central zone regions. Vacuum infiltration of nodules with salt solutions and subsequent cryo‐planing for SEM examination showed that open and water‐filled intercellular spaces could be differentiated. The potential is discussed for using this method to study the mechanism of diffusion barrier regulation in legume nodules.