Following cation and anion exchange chromatography, 1-aminocyclopropane-l-carboxylic acid (ACC) was converted to the 2,4-dinitrophenyl derivative and then purified by high-performance liquid chromatography (HPLC). After three HPLC steps, endogenous ACC was identified by GC-MS in the vascular cambium on the lower side of Pinus contorta Dougi. ssp. Iatifolia branches in association with compressionwood differentiation, but ACC was not detected in the opposite wood cambial region on the upper sides of the same branches.The possibility that ACC and ethylene have physiological roles in cambial activity and compressionwood tracheid differentiation is discussed.The well-established roles of C2H4 in promoting changed orientation of cell-wall microfibrils (1, 13) and intercellular air-space formation (8, 13) in higher-plant cells suggests that C2H4 may have roles in the development of similar changes between adjoining primary-walled cambial derivatives during their differentiation into compressionwood tracheids (21). Compressionwood normally develops only on gravitationally lower sides of conifer branches and leaning conifer stems, again suggesting involvement of C2H4 (22); however, prior to the demonstration of ACC4 being a watersoluble immediate precursor of C2H4 (2) The basal five internodes (forestry sense) from each branch provided the cambial tissue for extraction and GC-MS analysis. Tissues were harvested by bark peeling as previously described (19), pooling cambial zone plus differentiating xylem, and immediately submerging the tissues in liquid N2. The cambial region adjoining wide annual rings, comprised of red-brown compression wood tracheids and occurring on the gravitationally lower sides of the branch internodes, was harvested separately from the opposite wood cambial region. Tracheids were differentiating both sides of the branch internodes at time of harvesting. Extraction Procedure. Compressionwood and opposite wood cambial regions were extracted separately in darkness at 4°C with prechilled 80o (v/v) methanol (15:1, v/w) for 16 h, then filtered. The solid residue was reextracted with distilled H20 at 170C for 10 min, then filtered. The solid residue was again extracted at 4°C in darkness with prechilled 80% methanol for 2 h, then filtered, and the residual tissue finally was extracted several times in quick succession with distilled H20 at 17°C, filtering each time.The combined methanolic and aqueous extracts were reduced in vacuo at 35°C to an aqueous phase, transferred to 250-ml centrifuge bottles, frozen, thawed, and centrifuged at 20,000g for 1 h at 40C.