Wound healing in cucumber fruit (Cucumis sativus L., cv. Calypso) was studied using histological and degradative techniques. A thick exudate appeared at the wounded surface shortly after wounding. This material retarded water loss and possibly aided in the formation of sclerified parenchyma observed 24 hours after wounding. The sclerified material was positive to a modified Weisner stain, indicating lignification was occurring. Wound periderm (cork) was initiated directly beneath the sclerified parenchyma cells within 48 hours after wounding. The cork layers were positive to Sudan IV stain, indicating suberin was being formed. The rate of phellem development decreased by 6 days after wounding. By day 7, younger phellem cells and sclerified parenchyma cells were stained by Sudan IV. Degradation of the wound tissue by chemical procedures demonstrated that relatively large amounts of lignin and suberin were deposited during healing. Fragments from the lignin degradation Indicated that lignin was composed mainly of gualacyl and p-hydroxyphenyl residues. Suberin was found to contain mainly 1,16-hexadecane and 1,18-osctadecene decarboxylic acids detected as the silylated diol derivatives. Wound healing by plants has significant theoretical and prac- tical impact. Successful postharvest storage of plant organs de- pends on the ability of the plant material to resist invasion by pathogenic microorganisms. Commercially important plant or- gans generally are wounded during harvest and handling before storage. The frequency and severity of wounding varies with the 'nature of the harvested material, the environmental condi- tions during harvest, and the implements used for harvest and transporation. Since wounds can serve as avenues for microbial attack and moisture loss, rapid wound healing is required if organ decay and/or desiccation are to be avoided. Wound responses differ with regard to plant species and organ (El Hadidi, 1969; Rittinger et al., 1987). In many dicotyledons, wounds are closed by deposition of biopolymers in cells adja- cent to the wounded area, followed by formation of a wound periderm or cork beneath the sealed area. The deposited material has been shown, in some cases, to be suberin (Cottle and Ko- lattukudy, 1982) and lignin-like in others (Walter and Schadel, 1983). Suberin is believed to contain an aromatic domain, lig- nin-like in nature, that is covalently bonded to the cell wall and an aliphatic domain bonded to the aromatic regions (Kolattu- kudy, 1984). Suberized tissue generally has an affinity for lipid stains such as Sudan IV and, upon reductive depolymerization with Li Al H4, yields a family of mono- and di-alcohols with carbon chain lengths ranging from C16 through C30. Lignified tissue has little affinity for Sudan IV stain, but is highly reactive with Weisner stain (Walter and Schadel, 1983). Reductive de- polymerization yields only small amounts of mpno- and di-al- cohols, while alkaline oxidation gives relatively large amounts of p-hydroxybenz aldehyde and vanillin. Alkaline oxidation of suberized tissue gives similar degradation products, Thus, using