Circadian rhythms are widespread in nature and reflect the activity of an endogenous biological clock. In metazoans, the circadian system includes a central circadian clock in the brain as well as distinct clocks in peripheral tissues such as the retina or liver. Similarly, plants have distinct clocks in different cell layers and tissues. Here, we show that two different circadian clocks, distinguishable by their sensitivity to environmental temperature signals, regulate the transcription of genes that are expressed in the Arabidopsis thaliana cotyledon. One oscillator, which regulates CAB2 expression, responds preferentially to light-dark versus temperature cycles and fails to respond to the temperature step associated with release from stratification. The second oscillator, which regulates CAT3 expression, responds preferentially to temperature versus light-dark cycles and entrains to the release from stratification. Finally, the phase response curves of these two oscillators to cold pulses are distinct. The phase response curve of the oscillator component TOC1 to cold pulses is similar to that of CAB2, indicating that CAB2 is regulated by a TOC1-containing clock. The existence of two clocks, distinguishable on the basis of their sensitivity to temperature, provides an additional means by which plants may integrate both photoperiodic and temperature signals to respond to the changing seasons. T he circadian clock is an endogenous oscillator with an approximate period of 24 hr that can be synchronized, or entrained, to the exact period of daily oscillations in light and temperature (1). This enables an organism to phase its biological activities to the correct time of day. The sleep-wake cycle in humans, activity and eclosion rhythms in flies, and conidiation in Neurospora are rhythmic processes that display distinct phase angles with the environment (2). In the flowering plant Arabidopsis thaliana, the circadian clock phases the peak mRNA abundance of many genes to distinct times of day (3). Furthermore, the phase angle of specific circadian rhythms with the environmental light-dark (LD) cycle controls seasonal behavior such as flowering (4-6).The clock is temperature-compensated, meaning that the pace of the clock is more or less constant across a range of temperatures and fails to exhibit the acceleration with temperature that characterizes typical enzymatic reactions. Nonetheless, temperature serves as an important environmental time cue and entrainment to temperature cycles has been demonstrated in a number of systems (7,8). It is commonly assumed that light is the dominant environmental time cue for circadian clocks, although few studies have systematically compared light and temperature (9-12). In fact, temperature cycles applied antiphase to LD cycles set the phase angle of multiple rhythms, including CO 2 assimilation in Kalanchoë (13), ethylene production in sorghum (14), and conidiation in Neurospora (15).We compared the relative strengths of temperature cycles and LD cycles as determinants of the ph...