“…Tissues were processed in glutaraldhyde and OSO4 buffered with sodium cacodylate, triple-fixed with unbuflFered uranyl acetate, and embedded in Luft's epon (Luft, 1961). Sections for LM were stained with either Aniline blue black (total proteins; Fisher, 1968), Napthol black (total proteins; Tilton, 1978) or Methylene blue-azure II (nucleic acids; Humphrey and Pittman, 1974) and counterstained with basic fuchsin (carbonates; Humphrey and Pittman, 1974). Tissues for scanning electron microscopy (SFM) were cryofractured in liquid Ng, critical point dried with COg, and then coated with carbon and gold.…”