Photometric analysis of chloroplast movements in various phytochrome (phy) mutants of Arabidopsis showed that phyA, B, and D are not required for chloroplast movements because blue light (BL)-dependent chloroplast migration still occurs in these mutants. However, mutants lacking phyA or phyB showed an enhanced response at fluence rates of BL above 10 mol m Ϫ2 s Ϫ1 . Overexpression of phyA or phyB resulted in an enhancement of the low-light response. Analysis of chloroplast movements within the range of BL intensities in which the transition between the low-and high-light responses occur (1.5-15 mol m Ϫ2 s Ϫ1 ) revealed a transient increase in light transmittance through leaves, indicative of the high-light response, followed by a decrease in transmittance to a value below that measured before the BL treatment, indicative of the low-light response. A biphasic response was not observed for phyABD leaves exposed to the same fluence rate of BL, suggesting that phys play a role in modulating the transition between the low-and high-light chloroplast movement responses of Arabidopsis.Plants have evolved a number of developmental and physiological mechanisms that allow them to adapt to changes in their environment. Many of these pathways are modulated in response to various environmental stimuli such as light, gravity, temperature, and nutrient availability (Hangarter, 1997). In the case of light, plants possess a variety of photoreceptor molecules that are sensitive to the quality, quantity, and direction of light within the environment. The known photoreceptors of Arabidopsis include the phytochromes (phys A, B, C, D, and E), which mainly function to detect red light (RL) and far-red light (FRL) and two distinct classes of blue light (BL) photoreceptors, the "photolyase-like" cryptochromes (cry1, cry2, and cry3) and the phototropins (phot1 and phot2; Somers et al., 1991; Ahmad and Cashmore, 1993;Dehesh et al., 1993;Reed et al., 1993Reed et al., , 1994Clack et al., 1994;Liscum and Briggs, 1995;Guo et al., 1998: Kleine et al., 2003. The crys regulate inhibition of stem elongation, photomorphogenesis, entrainment of the circadian clock, leaf expansion, and anthocyanin production (Ahmad et al., 1995;Somers et al., 1998;Toth et al., 2001;Wang et al., 2001;Mockler et al., 2003). The phots mediate such BL responses as early phase inhibition of hypocotyl elongation (phot1), phototropism, stomatal regulation, and chloroplast movements (Liscum and Briggs, 1995;Christie et al., 1998;Lasceve et al., 1999;Folta and Spalding, 2001a;Kagawa et al., 2001;Kinoshita et al., 2001;Sakai et al., 2001).Analysis of mutants lacking one or more of these photoreceptors has led to a better understanding of how plants respond to changes in their light environment. It has become increasingly clear that these photoreceptors often act redundantly, synergistically, and/or antagonistically in several different light-mediated pathways (Casal and Boccalandro, 1995; Ahmad and Cashmore, 1997; Ahmad et al., 1998;Mockler et al., 1999;. For example, the co...