The effects of cyanide, anoxia, and temperatures varying from 2 to 42 C on the cell membrane electropotential difference (PD) of washed and freshly excised corn roots have been determined. Respiration rates of freshly excised root segments in response to cyanide and to varying temperatures were also measured. The ceDl membrane PD of roots which had been washed for 12 to 15 hours was almost insensitive to cyanide and anoxia but sensitive to low temperature. In contrast, the cell membrane PD of freshly excised roots was reversibly depolarized by all three treatments, cyanide depolarized from -117 to -86 milivolts and the sequential imposition of anoxia further lowered the PD to -69 milivolts. Anoxia applied first depolarized maximaDy and the PD was not further lowered by sequential cyanide treatment. Arrhenius plot analysis of the temperature response of respiration showed an apparent transition at 13 C with an activation energy of 20.0 kilocalories per mole below and 8.8 kilocalories per mole above the transition temperatures. The energy of activation for repolarization of PD is much higher, 53.4 kilocalories per mole below 7 to 8 C and 25.4 kilocalories per mole above this apparent transition. The energy requirement for polarization of the ceOl membrane PD was calculated based on the temperature responses of the ceOl membrane PD and respiration. It was estimated that 3.5% of the energy output from respiration at 22 C is required for cell polarization. It is unlikely that ion transport is limited by energy availability below the 8C transition in this chili sensitive species.Cells of higher plants typically maintain a cell PD4 of about 100 mv, interior negative. This cell PD has been shown to have two components in corn roots and in other higher plants (1,6,7,9). One of the components is of a diffusive nature and contributes about one-half of the total potential (12). The other component, generated by the activity ofelectrogenic ion pumps, can be blocked by treating the tissue with inhibitors of mitochondrial electron transport such as cyanide (7, 17), carbon monoxide (1), azide (20), uncouplers such as fluorocarbonyl cyanide phenylhydrazone (6) and DNP (7,12). Anoxia (10), and low temperatures (8,20) that the cell PD in washed pea and oat stem tissue is sensitive to CN-. Preliminary studies on the relationship of PD to respiratory activity in corn indicated that PD in this species is not affected by CN-when roots are washed by the protocol used for oats and peas by Higinbotham et al (12). A portion of this study examines the effects of CN-, anoxia, and low temperature on washed and freshly excised corn roots. The restriction of respiration by low temperature in chill sensitive species has been amply documented (2,4,5,19). The reduction of respiratory function has been correlated with reduced ion uptake (5). This study allows an analysis of the relationship between low temperature inhibition of respiratory activity and the cell PD in this chill sensitive species.The results are used to define further the r...