Mitochondria isolated from 3-day-old etiolated corn shoots (Zea mays L.) can be categorized into three separate groups, each group characteristic of the cell type from which the mitochondria were isolated. Phloem sieve tubes and some adjacent parenchyma cells contain (12,24,26). Swelling involves the unfolding of the inner membrane and a decrease in the amorphous matrix, while contraction involves the infolding of the inner membrane and increase in matrix density. The presence of contracted, partially swollen, and swollen mitochondria in experimental in vitro preparations that should contain only contracted (or swollen) mitochondria is believed to result from mitochondria responding at different rates (26). A ready reversibility has been reported to exist between swollen, partially swollen, and contracted mitochondria (24).In vivo differences in the number of cristae and amount of amorphous matrix in different cell types for several species of plants have been reported (5, 7-9, 13, 16, 19, 22). Chrispeels et al. (6) Isolated mitochondria were fixed either while they were suspended or after being pelleted at 12,000 rpm for 10 min. Fixatives for isolated mitochondria or intact shoots were 1 or 2% glutaraldehyde either in 0.1 M phosphate buffer or in 0.2 M cacodylate buffer (pH 7.4) followed by 1 % OsO in the respective buffer; or only 1 % OSO4 in 0.1 M phosphate buffer or 0.2 M cacodylate buffer. Dehydration was in a graded ethyl alcohol series, and propylene oxide was used as a solvent for the Epon embedment (15).In vivo mitochondrial contractions were obtained by treating 1-mm thick sections of corn shoots with 2.5 mM 2DOG2 for 20 min (11). The sections were then fixed in 2% glutaraldehyde in 0.2 M cacodylate buffer.One-,um thick plastic sections of whole plant material were cut and observed with phase contrast optics for orientation purposes. Subsequently, thin plastic sections were cut from the adjacent area of the block. All thin sections were observed on an RCA EMU4 or Siemens Elmiskop I electron microscope after staining in uranyl acetate (23) and lead citrate (21).Areas of I. C. and 0. C. of type III mitochondria were determined by superimposing a dot grid on a micrograph and counting dots falling in the compartments.
RESULTSMitochondrial profiles fell into three readily recognizable types and were classified according to the type which they most