Electronic Journal of Biotechnology
On-line version ISSN 0717-3458
Electron. J. Biotechnol. vol.8 no.1 Valparaíso Apr. 2005
Growth responses of Betula pendula ecotypes to red and far-red light
Berhanu A. Tsegay*
Jorunn E. Olsen
Jorgen M. Molmann
Arild Ernsten †
Financial support: This research was funded by the Norwegian Research Council.
The effect of Red light (R), Far-red light (FR) and R/FR combinations on shoot growth of latitudinal ecotypes of B. pendula was studied using special diodes that emit monochromatic lights. When a 12 hrs PAR (110 µmol m-2 s-1) was extended with R, FR or R/FR ratios, lower intensities of monochromatic lights could not prevent growth cessation. At 25 µmol m-2 s-1, FR compared to R enhanced stem elongation in all ecotypes. This was due to the inhibitive effect of R on internode elongation. When day-length was extended by R/FR at various ratios, there was continuous shoot elongation, but was found to be declining with increasing ratios. The more the R, the shorter were the internodes of each plant. B. pendula ecotypes produced branches when PAR light during the day was extended by incandescent light, but did not do so when the light extensions were made by monochromatic R or FR or their combination. Branching increased with decreasing latitude of the ecotype.
Light, as a main environmental trigger, plays a central role in regulating plant development. Most terrestrial plants grow by selective absorption of natural light from the sun. The most effective components of the spectrum of light are red (R), far-red (FR), and blue. These lights are involved in the regulation of photosynthesis, pigment biosynthesis, photoperiodism, phototropism, and photomorphogensis. The photomorphogenetic response of plants to light include, among others, seed germination, inhibition of hypocotyl elongation, cotyledon and leaf expansion, pigment synthesis, stem elongation, and induction of flowering (Weller et al. 2000).
At least three known photoreceptor proteins monitor the quantity and quality of the incoming light. These are the phytochromes, the cryptochromes and phototropins, as well as the UV-B photoreceptors. Phytochromes are the most studied of these receptors. They are soluble chromoproteins synthesized in the dark, in their physiologically inactive form, red light perceiving phytochrome (Pr). Upon irradiation with R, phytochromes are converted to their active form, far red light perceiving phytochrome (Pfr), which in turn decay back to, or are photolytically reconverted by FR to the original inactive form, Pr. This cyclic reversibility enables plants to respond, among others, to changes in spectral composition of light and to optimise growth and development during their whole life cycle. In Arabdopsis, there are at least five genes (PHYA to PHYE) encoding five groups of phytochromes, phyA to phyE (Hauser et al. 1997; Gil et al. 2000; Weller et al. 2000). These phytochromes monitor a wide array of light parameters, including the onset of light, the directional vector of ambient light, the ratio of R to FR, a range of photon fluences and the wavelength distribution of light during the day as well as at the end of the photoperiod (Hauser et al. 1997; Olsen and Junttila, 2002). The most studied phytochromes are phytochrome A (phyA) and phytochrome B (phyB). PhyA mediates the very low fluence response (VLFR, under multiple wavelengths of light) and high irradiation response (HIR, under continuous FR). PhyB is responsible for the R/FR - reversible low fluence response, LFR (Chory, 1997).
In temperate zone woody plants, short days (SDs) induce growth cessation and bud dormancy. However, when SDs are extended with light extensions of appropriate spectral composition, plants perceive them as long days (LDs). Such perception depends on the light requirement of those plants under consideration. Latitudinal ecotypes of northern tree species have different responses to light quality (Håbjørg, 1972; Junttila and Kaurin, 1985; Clapham et al. 1998), which could indicate differences in composition of their phytochrome systems. In experiments using light sources enriched in R or FR light, differences in FR light requirement by latitudinal ecotypes have been indicated. For example, in Salix pentandra, high R/FR ratio during the night extension did not produce a LD effect in a northern ecotype but did so in a southern one (Junttila and Kaurin, 1985). Moreover, over-expression of phyA changed (shortened) the critical photoperiod of hybrid aspen (Olsen et al. 1997). However, such responses have not been tested with monochromatic lights or defined R/FR ratios. B. pendula ecotypes grow continuously when 12 hrs PAR light is extended with incandescent bulbs of about 10 µmol m-2 s-1 (Berhanu, 2002). But, the responses of the latitudinal ecotypes upon extension of the PAR light with R, FR or various ratios of R and FR have not been studied. Moreover, there is no information so far about possible differences between photoperiodic ecotypes at the phytochrome level although phytochrome genes have been cloned from both conifers and deciduous species.- This study aimed at comparing the vegetative growth responses of latitudinal ecotypes of B. pendula to monochromatic R and FR, and to various combinations of R and FR.
Light emitting diodes (Q-BEAM 2200, Quantum Devices, Inc. 112 Orbison Barneveld, WI 53507, USA) were used as sources of R and FR lights. In these light sources, both irradiances and R: FR ratios could be changed independently. Photon fluence rates of R with maximum emission at about 667 nm were measured using a Datalogger (Model L1 - 1000 Serial No. LDL 3527, USA) with the light sensor, LI-CDR Quantum, Q2012 attached to it. Fluence rates of FR at maximum emission of 739 nm were adjusted in relation to the quantified R. These light treatments were established in trolleys each having a size of 50 x 50 cm. The light source heads of the LEDs were mounted on a board at about the top-centre of each trolley, providing almost uniform intensities at various parts of the trolleys. A fourth trolley was prepared for dark control. All trolleys were covered on all sides by curtain to prevent possible entrance of light beams from one trolley to the other.
Photosynthetically active radiation, about 110 µmol m-2 s-1, was made available by installing fluorescent lamps (Phillips TLD 58/840) in each trolley (Figure 1). This was made by adjusting the distance between the lump and the shoot apices. Hence, all plants were treated with PAR light for 12 hrs and with R, FR, R/FR or dark for the other 12 hrs of each day. Effects of monochromatic R and FR on cessation of growth of seedlings were studied at intensities of 0.5, 1.0, 9.5, and 25.0 µmol m-2 s-1. Various R: FR ratios (1.0, 1.5, 2.0, 2.5, 3.0, 5.0, and 7.5) at 25 µmol m-2 s-1 were also used in these growth cessation experiments.
This experiment was conducted in the phytotrone, the University of Tromsø. Seedlings of three latitudinal ecotypes of B. pendula Roth were used. Seeds were collected from southern Norway (59ºN), the middle of Norway (64ºN) and northern Norway (67ºN). The seeds were stratified in moist sand for about a month at 0.5ºC and germinated in continuous light (180 - 200 µmol m-2 s-1) from fluorescent tubes (Philips TLD 58 / 840) and incandescent bulbs at 18ºC. After germination, seedlings were transplanted into 12 cm diameter pot, 4 to 5 plants per pot. The growth medium was fertilized peat: perilite: and sand (6:3:1, v/v). Plants were watered daily with a complete nutrient solution (Junttila, 1980). Day-length treatments were established in the phytotrone compartments. The main light period of 12 hrs (08:00 - 20:00) had 150 µmol m-2 s-1 PAR from fluorescent tubes and additional 10 µmol m-2 s-1 from incandescent bulbs. The photoperiodic treatments were established by extending the light period with 10 µmol m-2 s-1 light from incandescent bulbs (Osram, 75 W). Temperature in the compartments was 18 ± 0.5ºC and the RH was 78%, which corresponds to 0.5 kPa water vapour pressure deficit. When the plants reached the size of 2 to 3 cm, they were transferred to their respective light treatments (12 hrs PAR + 12 hrs extension with R, FR, R/FR or dark). There were four pots per treatment per ecotype, each pot containing 4 plants. Stem length and numbers of new leaves were recorded every week for one month.
Statistical analyses were carried out using Abacus Concepts (Haycock et al. 1994), Stat View (Abacus Concepts, Inc., Berkeley, CA, 12994). Standard deviations or standard errors were presented
About 2 - 3 cm long plants, which had been grown in LD of 12 hrs PAR plus 12 hrs incandescent light were treated by 12 hrs PAR extended with 12 hrs R, FR at various intensities, or R/FR at various ratios for 4 weeks.
Generally, the intermediate ecotype grew slower than the other ecotypes. Average growth increment, means of all R and FR irradiances, was 129 ± 12.4, 108 ± 14.6, and 121 ± 11.6 mm for the southern, intermediate, and northern ecotype, respectively. Differences between these values were not, however, statistically significant. As shown in Fig 2., FR (compared to R) enhanced stem elongation in all ecotypes. The difference between the effect of FR and R at the two highest irradiances was highly significant (P < 0.0001). Growth increment during the experiment, as a mean of all ecotypes and irradiances, was 139 ± 11.2 and 100 ± 8.1 mm for FR and R, respectively. These values were different at P = 0.007. Stem elongation increased with increasing irradiance both for R and FR. Although the two lowest irradiances, 0.5 and 1.0 µmol m-2 s-1, enhanced growth compared to SD, they could not prevent cessation of elongation growth (Figure 2). At irradiances of 9.5 and 25.0 µmol m-2 s-1, elongation growth was sustained in all ecotypes both by FR and R day-length extensions. Besides, there was no statistically significant interaction between ecotype and light quality or irradiances (Table 1).
Light quality had significant influence on internode length but not on the number of leaves. However, leaf number increased with increasing irradiance (Figure 3). The mean leaf number of all ecotypes at all irradiances was 4.2 and 4.8 in FR and R, respectively. These values are statistically similar (P = 0.2962). The northernmost ecotype had less number of leaves compared to the southernmost.
When 12 hrs PAR light was extended by various R/FR ratios, shoot growth (stem elongation and production of new leaves) was continuous in all treatments. The mean stem elongation of all treatments was 215 ± 7.4, 159 ± 6.1 and 208 ± 8.5 mm for the southern, the intermediate and the northern ecotype, respectively. The intermediate ecotype was responding differently from the other two (P < 0.0001; critical difference of 17.47). Although stem elongation was continuous, the rate of growth declined with increasing R/FR ratios, especially in the southern and the northern ecotypes (Figure 4a). The mean values of elongation growth of all ecotypes were 182 ± 9, 238.9 ± 15.7, 207 ± 16.5, 199 ± 17.2, 192 ± 14.5, 199 ± 16.1, 178 ± 8, and 156 ± 6.7 mm in R/FR of 0.5, 1.0, 1.5, 2.0, 2.5, 3.0, 5.0, and 7.5, respectively. Stem lengths at the lowest (0.5) and two highest (5.0 and 7.5) R/FR ratios were significantly shorter (P < 0.05) than in ratios of 1.0 - 3.0. In R/FR ratios of 1.0 - 3.0, growth was almost identical to LD control in the southern and the northern ecotypes (data not given). No significant effect of R/FR ratios on production of new leaves was detected (Figure 4b). Consequently, internode length decreased with increasing R/FR ratio (Figure 4c). Regression of internode length against R/FR ratio was highly significant (see equations on Figure 4c).
Another observation made during the experiments was that the branching pattern was dependent on the light treatment and on the ecotype. Plants grown in LDs (12 hrs PAR + 12 hrs incandescent) produced branches while there was no branching in those treatments where the day-length extension was made by monochromatic R or FR, or their combination (Figure 5). Moreover, rate of branching decreased with increasing latitude of the ecotype.
Extension of 12 hrs PAR light with 12 hrs FR or R at 0.5 or 1.0 µmol m-2 s-1 could not prevent cessation of growth in B. pendula ecotypes. At irradiances of 9.5 and 25.0 µmol m-2 s-1 growth was sustained, but the seedlings at R had stunted growth compared to those treated with FR (Figure 2). When the plants were irradiated with different R/FR ratios, they were able to grow continuously. These results essentially proved the combined effect of the putative light receptors, phyA and phyB. The northernmost ecotype had longer internodes than the southern ones (Figure 3). However, the total stem length was not different from the southernmost ecotype (Figure 2). Hence, the requirement of FR at the tested irradiances was similar to all ecotypes. Moreover, none of the R/FR ratios used stopped growth. However, there was a declining rate of stem elongation with increasing R/FR ratio (Figure 4a). Unlike stem elongation, the number of leaves remained constant in all R/FR ratios (Figure 4b). Consequently, there was a sharp decline in internode length with increasing R/FR-ratio (Figure 4c). R/FR-ratios between 1 and 3 (inclusive) resulted in best growth in all ecotypes, comparable to growth of those plants grown in LD PAR light extended with incandescent light, R/FR = ca. 0.7.
Differences in FR light requirement for growth extension were shown by latitudinal ecotypes of Salix pentandra (Junttila and Kaurin, 1985), Picea abies (Clapham et al. 1998) and Pinus sylvestris (Clapham et al. 2002). When the day-length was extended with FR-poor lamps, the southern ecotypes (south of 61 - 64ºN) continued to grow while the northern ones ceased growth. This was not the case in B. pendula ecotypes used in this study. As FR decreased (R/FR = 7.5), extension growth was reduced, but all ecotypes behaved similarly. Furthermore, the reduced elongation was due to the decline in internode elongation. Although the explanation may not be easy at this point, it is worth mentioning some possible reasons. The first possibility is the very difference of the plant species. While it is logical to expect B. pendula to behave in a similar way to Salix pentandra, the other species, Picea abies and Pinus sylvestris are phylogenetically far away from B. pendula. Besides, the treatment of the latter two was 8 hrs PAR and 16 hrs FR-poor day extension. The second possible factor may be the intensity of the light treatment. While Clapham et al. 2002 used 230 µmol m-2 s-1 from incandescent during 8 hrs day and extended it by 16 hrs of 40 µmol m-2 s-1 from FR-poor white fluorescent light, in this experiment 110 µmol m-2 s-1 from fluorescent tubes during 12 hrs day was extended by 25 µmol m-2 s-1 FR only or R/FR at various ratios from light emitting diodes.
When a 12 hrs PAR (150 µmol m-2 s-1 plus 10 µmol m-2 s-1) was extended by incandescent light (10 µmol m-2 s-1) there was branching by most plants of the southern and the intermediate ecotypes. Branching increased with decreasing latitude of the ecotypes (Figure 5). This phenomenon could be due to light spectra other than R and FR in the incandescent light, especially blue light. Induction of side branching by blue light in a moss Physcomitrella patens protonemal colonies was reported by Imaizumi et al. (2002). The induction of side branching was believed to be a result of the suppression of auxin induced gene expression by cryptochrome-mediated signals. In the classical blue light induced phototropism of shaded and illuminated coleoptiles of cereals (Taiz and Zeiger, 1998), bending is believed to be the result of the lateral re-distribution of auxin (caused by blue light) and differential rates of cell elongation. The increased of branching in mixed lights (incandescent light) and the absence of branching in R, FR or R+FR treated plants in this experiment may give clue to the role of blue light in inducing branches in trees as well. If this is true, the response to the signal by the different ecotypes of B. pendula was different: decreasing with increasing latitude of origin.
Of the B. pendula ecotypes used in this study, the intermediate one was behaving differently (had slower growth rate) from the southern and the northern ones. Thus, it is likely that these differences were because of other factors than the latitudinal origin of the ecotype. For example, it is possible that differences in seed lot (storage) could have affected photomorphogenesis of the seedlings. Another factor that could interfere in the growth and development of seedlings is the climatic and nutritional status of the mother plants. If the growth environment of the mother plants were favourable, the seeds would properly mature and store enough food, which, in turn, directly influences the success of germination and development of the seedlings. It is also possible that the seed lot of the intermediate ecotype does not fully (completely) represent the ecotype genetically. While studying the adaptive properties of Picea abies progenies, Johnsen and Skrøppa (1996) concluded that both the genetic constitutions of the parents and the prevailing environmental conditions during sexual reproduction could alter the phenotypic performance of the progenies. They further elaborated this issue and put the reproductive environment to be additional evolutionary force to mutation, natural selection and gene flow (Johnsen et al. 1996; Skrøppa and Johnsen, 2000). Thus, the phenotypic anomality of the intermediate ecotype might have been caused by several factors.
In conclusion, R and FR at higher intensities influenced shoot elongation differently. FR at about 9.5 - 25 µmol m-2 s-1 sustained continuous elongation of shoots of all ecotypes compared to R. However, the combined effect of R and FR at various ratios and at an intensity of 25 µmol m-2 s-1 had a significantly higher effect. This clearly showed the combined effect of phyA and phyB in all B. pendula ecotypes.
The authors are grateful to the staff of the Climate Laboratory, University of Tromso, for offering us their facility for so long time. Mr. Tsefaye Dagnew, a senior lecturer of English at Bahir Dar University, is also duly acknowledged for his language editorial service.
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