Juvenile phase English ivy (Hedera helix L.) plants accumulate anthocyanin pigment in the hypodermis of stems and petioles, whereas genetically identical plants of the mature phase do not.
Photoperiod is an important signal controlling the onset of dormancy in perennial plants. Short days typically induce growth cessation, the initiation of cold acclimation, the formation of a terminal bud. bud dormancy and other adaptive responses. Photoperiodic ecotypes have evolved in many species with large latitudinal distributions. The photoperiodic responses of two northern (53°35′ and 53°50′N) and two southern (34°10′ and 40°32′N) genotypes of black cottonwood (Populus trichocarpa Torr. & Gray) were characterized by growing trees under a range of photoperiods in the greenhouse and growth chamber. Short days induced bud set in both ecotypes. resulting in trees with fewer leaves and less height growth than trees grown under long days. Short days also enhanced anthocyanin accumulation in the northern ecotype and decreased branching of the southernmost genotype. Two aspects of the photoperiodic response were evaluated for each trail: critical photoperiod. which was defined as the longest photoperiod that elicited a short‐day response, and photoperiodic sensitivity, which was defined as the change in response per unit change in photoperiod. For each of the traits analyzed, the northern ecotype had a longer critical photoperiod and greater photoperiodic sensitivity than did the southern ecotype. The short critical photoperiod and reduced photoperiodic sensitivity of the southern ecotype resulted in a significant delay in bud set compared to that of the northern ecotype, even under a 9‐h photoperiod. Typically, photoperiodic ecotypes have been characterized as having different critical photoperiods. Ecotypic differences in photoperiodic sensitivity, however, indicate that differences in the photoperiodic response curves cannot be completely described by the critical photoperiod alone. These results also suggest that the critical photoperiod. photoperiodic sensitivity and speed of bud set have a common physiological basis. Bud set occurred earlier hi the northern ecotype primarily because bud scale leaves were initiated earlier. For one of the northern genotypes, leaf primordia that were initialed under long days subsequently differentiated into bud scale leaves after the trees were transferred to a 9‐h photoperiod. This demonstrates that primordia initiated under long days are not necessarily committed to becoming foliage leaves. The response to photoperiod did not differ appreciably between the greenhouse and growth chamber conditions that were tested.
The phytochrome photoreceptors play important roles in the photoperiodic control of vegetative bud set, growth cessation, dormancy induction, and cold-hardiness in trees. Interestingly, ecotypic differences in photoperiodic responses are observed in many temperate-zone tree species. Northern and southern ecotypes of black cottonwood (Populus trichocarpa Torr. & Gray), for example, exhibit marked differences in the timing of short-day-induced bud set and growth cessation, and these responses are controlled by phytochrome. Therefore, as a first step toward determining the molecular genetic basis of photoperiodic ecotypes in trees, we characterized the phytochrome gene (PHY) family in black cottonwood. We recovered fragments of one PHYA and two PHYB using PCR-based cloning and by screening a genomic library. Results from Southern analyses confirmed that black cottonwood has one PHYA locus and two PHYB loci, which we arbitrarily designated PHYB1 and PHYB2. Phylogenetic analyses which included PHY from black cottonwood, Arabidopsis thaliana and tomato (Solanum lycopersicum) suggest that the PHYB/D duplications in these species occurred independently. When Southern blots were probed with PHYC, PHYE, and PHYE heterologous probes, the strongest bands that we detected were those of black cottonwood PHYA and/or PHYB. These results suggest that black cottonwood lacks members of the PHYC/F and PHYE subfamilies. Although black cottonwood could contain additional PHY that are distantly related to known angiosperm PHY, our results imply that the PHY family of black cottonwood is less complex than that of other well-characterized dicot species such as Arabidopsis and tomato. Based on Southern analyses of five black cottonwood genotypes representing three photoperiodic ecotypes, substantial polymorphism was detected for at least one of the PHYB loci but not for the PHYA locus. The novel character of the PHY family in black cottonwood, as well as the differences in polymorphism we observed between the PHYA and PHYB subfamilies, indicates that a number of fundamental macro- and microevolutionary questions remain to be answered about the PHY family in dicots.
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