Thanks for the link, and 'm so impressed with what i read I felt compelled to steal it:
After germination, seedlings follow one of two developmental patterns. Skotomorphogenesis (or etiolation) in the dark is characterized by long hypocotyls, closed cotyledons protected by apical hooks in A. thaliana, and the development of
proplastids into
etioplasts. By contrast, growth in the light results in photomorphogenesis (or de-etiolation) characterized by short hypocotyls, expanded open cotyledons and the development of mature green chloroplasts that can photosynthesize. A wide spectrum of light, in particular far-red, red, blue and ultraviolet (UV) light conditions, induces photomorphogenesis. PHYA is the primary photoreceptor under far-red light in A. thaliana, whereas PHYB has a major role under white or red light with the aid of PHYA, PHYC and PHYD. Rice PHYA and PHYB equally contribute to seedling photomorphogenesis under red light and both rice PHYA and PHYC are involved in far-red light responses
148. Both CRY1 and CRY2 cryptochromes are responsible for photomorphogenesis under blue and UVA light.
When plants grow in close proximity there is competition for light. Higher plants have evolved an impressive capacity to avoid shade. A plant canopy is associated with a reduction in the ratio of red:far-red light. Changes in the red:far-red ratio are detected as a change in the relative proportions of Pr and Pfr forms of phytochromes and PHYB has the most significant role
5.
The perception of photoperiod (or day length) is crucial for plants to adjust their development to fit into annual seasonal changes. The interaction of light signals with intrinsic circadian rhythms measures changes in day length. In A. thaliana, both phytochromes and cryptochromes contribute to synchronizing the circadian clock. The perception of day length is an important signal in the control of flowering.
Several other transient developmental processes, including phototropism, chloroplast movement and stomatal opening, are under light control mainly through phototropins
146. These rapid light-responsive processes are not under extensive transcriptional regulation, and are therefore beyond the scope of this Review