Light modulation of the gravitropic set-point angle (GSA).

A study has been made of the means by which light influences the gravitropic set-point angle (GSA) of the nodes of Tradescantia and the hypocotyls of the lazy-2 mutant of tomato. In light-grown Tradescantia there is a light-regulated developmental change in the GSA with the magnitude of this change being dependent on the photon flux density of white light. The photosynthetic inhibitor DCMU abolished the effect of white light. Low fluence rates of red light had no significant effect on the GSA of Tradescantia: It was concluded that there is an interaction between photosynthesis and the GSA in Tradescantia: The light-induced reduction of the GSA of the hypocotyl of lazy-2 tomato has previously been assumed to be solely an action of light acting via phytochrome. However, it can be shown that the GSA of hypocotyls of lazy-2 seedlings grown in white light is sensitive to DCMU and norflurazon treatment, hence the light effects on the GSA of an organ can be mediated via both phytochrome and photosynthesis. The implication of these findings to the study of gravitropism is discussed.     

GROWTH REGULATION BY ETHYLENE IN FERN GAMETOPHYTES. IV. INVOLVEMENT OF PHOTOSYNTHESIS IN OVERCOMING ETHYLENE INHIBITION OF SPORE GERMINATION

The inhibitory effects of ethylene on spore germination were investigated. In darkness spore germination was completely inhibited by 10 μ1 · 1⁻¹ ethylene. Light partially overcame this inhibition, and the effect of continuous irradiation with white fluorescent light saturated at about 450 μW · cm⁻². Monochromatic red, blue and far-red light were effective in overcoming ethylene inhibition, whereas green was not. Short periodic exposures to red or far-red light were not sufficient to overcome ethylene inhibition. This suggested that phytochrome was not involved. The photosynthetic inhibitor DCMU blocked the effect of light. Infrared gas analysis showed that photosynthesis saturated at about 450 μW · cm⁻² in white light. Red, blue and far-red light were more efficient photosynthetically than green light; DCMU blocked photosynthesis. Normalized curves of photosynthesis and germination vs. light intensity showed a similar dependence on light energy. It was concluded that light appears to overcome the inhibitory effects of ethylene through some process dependent on photosynthesis.     

Ethylene and the Responses to Light of Rice Seedlings

The growth of rice seedlings (Oryza satira L.) in the presence of ethylene caused a change in the response to light of coleoptile elongation. In plants grown in air without added ethylene coleoptile elongation was promoted by red, far-red and yellow-green light only in very young seedlings; in older plants irradiation inhibited the growth of the coleoptile. The effect of growing plants in the presence of ethylene was to prolong the period during which light promoted coleoptile growth. Elongation of the first internode was inhibited by light whether or not the seedlings were grown in the presence of ethylene. A correlation existed between the growth effect of an irradiation and the initial decay rate of phytochrome which was established by the treatment. Regardless of wave length, light sources whose intensities were adjusted to produce a decay rate of about 10% per hour or less induced a moderate rate of coleoptile elongation which persisted for a relatively long period. Irradiation with red or yellow-green light of higher intensity which produced a higher rate of phytochrome decay induced a higher rate of coleoptile elongation, but growth stopped after several hours. Other observations, however, showed that one cannot establish a general simple correlation between the rate of elongation of rice coleoptiles under light and the status of measurable phytochrome in the plant.     

Light-controlled Leaf Expansion in Peas Grown under Different Light Conditions

Several photosystems control leaf expansion in Alaska peas (Pisum sativum). Phytochrome is known to control expansion in dark-grown peas. But plants exposed briefly to red light are insensitive to phytochrome, an insensitivity that is itself phytochrome-produced. Leaf expansion in these plants is promoted by 440 or 630 nm of light (probably mediated by protochlorophyll). Plants grown in white fluorescent light required simultaneous exposure to high intensity blue and yellow light for promotion of leaf expansion. Since these results parallel studies on light-controlled inhibition of stem elongation, shoot growth as a whole is coordinated by these photosystems. Such coordination might be a mechanism of plant competition for light.     

Photomorphogenesis, Photosynthesis, and Early Growth of Primary Leaves of Phaseolus vulgaris

The response of leaf tissue to white, blue, red, and far-redlight has been examined. Leaves on plants grown in darknessshow increased cell number, cell volume, and area when exposedto long periods (up to 48 h) of low-intensity red, blue, orfar-red radiation. This is believed to be a photomorphogenicresponse which does not involve photosynthesis. Leaves fromplants exposed to white light during germination do not usuallyrespond to red, blue, or far-red light. An exception to thiswas found for leaf discs which showed a larger increase in areathan the dark controls following exposure to far-red light for24 h. Leaf tissue from light-grown plants responds to high-intensitywhite light, probably through photosynthesis. Discs cut fromdark-grown plants and cultured in white light grow equally wellin air and CO₂-free conditions. Application of the photosyntheticinhibitor DCMU reduces growth and chlorophyll formation, however. It is concluded that light, perhaps acting through the phytochromemechanism, has initially a number of morphogenic effects includinginitiation of development of the photosynthetic apparatus. Theresponses to photomorphogenically active radiation do not persistand light effects through photosynthesis are rapidly initiatedand dominate the later stages of leaf growth.     

Phytochrome-mediated phototropism inAdiantum cuneatum young leaves

Phototropism of youngAdiantum fern leaves is induced by red light as well as blue light. The red light response is mediated by phytochrome. This is the first evidence of phytochrome action in diploid fern tissue. The blue light response is mainly mediated not by phytochrome, but probably by a blue light-absorbing pigment as in the case of almost all plants and fungi. The red light-induced phototropism becomes detectable within 2 hr after the onset of unilateral light. The highest bending rate is about 10 degrees/hr, which occurs between 3–5 hr after the induction of the tropic response. The bending region is about 6–8 mm from the highest point of the coiled crozier where the growth rate becomes slow.     

Effects of the herbicide san 9789 on photomorphogenic responses

The herbicide, 4-chloro-5-(methylamino)-2-(α,α,α-trifluoro-m-tolyl)- 3(2H)-pyridazinone (San 9789), an inhibitor that prevents both carotenoid and chlorophyll accumulation and normal chloroplast development in white light, does not affect the physiological effectiveness of phytochrome in dark-and light-grown plants. Red/far red reversibility of growth inhibition, stimulation of anthocyanin synthesis, and stimulation of phenylalanine ammonia-lyase synthesis are not significantly different in plants grown with and without San 9789. Despite the complete absence of photosynthesis, flowering could be induced in the long day plant Hordeum vulgare L. when sucrose was provided to the leaves. Since the nonphotochemical reactions of phytochrome also are not affected by the herbicide, San 9789 may be used as a tool to study the phytochrome system spectrophotometrically in plants grown for relatively long periods under high intensity white light.     

Altered Phytochrome Regulation of Greening in an aurea Mutant of Tomato

A brief pulse of red light accelerates chlorophyll accumulation upon subsequent transfer of dark-grown tomato (Lycopersicon esculentum) seedlings to continuous white light. Such potentiation of greening was compared in wild type and an aurea mutant W616. This mutant has been the subject of recent studies of phytochrome phototransduction; its dark-grown seedlings are deficient in phytochrome, and light-grown plants have yellow-green leaves. The rate of greening was slower in the mutant, but the extent (relative to the dark control) of potentiation by the red pulse was similar to that in the wild type. In the wild type, the fluence-response curve for potentiation of greening indicates substantial components in the VLF (very low fluence) and LF (low fluence) ranges. Far-red light could only partially reverse the effect of red. In the aurea mutant, only red light in the LF range was effective, and the effect of red was completely reversed by far-red light. When grown in total darkness, aurea seedlings are also deficient in photoconvertible PChl(ide). Upon transfer to white light, the aurea mutant was defective in both the abundance and light regulation of the light-harvesting chlorophyll a/b binding polypeptide(s) [LHC(II)]. The results are consistent with the VLF response in greening being mediated by phytochrome. Furthermore, the data support the hypothesis that light modulates LHC(II) levels through its control of the synthesis of both chlorophyll and its LHC(II) apoproteins. Some, but not all, aspects of the aurea phenotype can be accounted for by the deficiency in photoreception by phytochrome.     

Visualization of a rapid,red/far-red light-dependent reaction by centrifuge microscopy

Summary Using a centrifuge microscope with stroboscopic illumination, we examined the effects of light irradiation on the passive movement of chloroplasts in dark-adapted mesophyll cells ofVallisneria gigantea. While irradiation with red light accelerates the passive gliding of chloroplasts produced by centrifugal force, irradiation with far-red light negates this effect. Irradiation with blue light does not accelerate the passive gliding, while red light is completely effective even in the presence of 3-(3,4-dichlorophenyl)-1,1-dimethylurea, an inhibitor of photosynthesis. An apparently active movement of chloroplasts can be induced by irradiation with red or blue light only in the presence of the far-red light-absorbing form of phytochrome. The significance of the reaction in the light with respect to the regulation of cytoplasmic streaming is discussed.Abbreviations APW artificial pond water - CMS centrifuge microscope of the stroboscopic type - DCMU 3-(3,4-dichlorophenyl)-1,1-dimethylurea - Pfr phytochrome, far-red light-absorbing form - Pr phytochrome, red light-absorbing form     

Analysis of phytochrome kinetics in light-grown Avena sativa L. seedlings

The phytochrome content, the rate of phytochrome accumulation after a light/dark transition and the rate of phytochrome destruction after a 1.5 d reaccumulation period in darkness were measured in light grown Avena sativa L. seedlings. The results using spectrophotometrical methods (Norflurazon treated seedlings) and the radio-immunoassay (RIA) (green seedlings) were almost identical. The rate of phytochrome synthesis was analysed by measuring the activity of poly(A⁺)-RNA coding for the phytochrome apoprotein. It was demonstrated that the rate of phytochrome synthesis is different in light and in dark. These results were confirmed by measuring the incorporation of radioactive label in vivo. Five minutes red (and 5 min far-red) light strongly reduces the rate of phytochrome synthesis. Even after prolonged dark periods only 50% of the initial rate of phytochrome synthesis is recovered for light and dark grown seedlings which received one red light pulse.     

The germination characteristics of phytochrome-deficient aurea mutant tomato seeds

The role of light reactions in anthocyanin synthesis was studied in both attached and detached corollas of Petunia hybrida (cv. Hit Parade Rosa), the latter grown in vitro in media containing 150 m M sucrose and 50 μ M gibberellic acid (GA). Light was essential for the synthesis of anthocyanin in detached corollas, whereas in intact corollas its effect was only to enhance anthocyanin synthesis. Continuous white light at a fluence rate of at least 20 μmol m⁻² s⁻¹ was needed for anthocyanin synthesis in detached corollas. Blue light was more effective than red or green, and far-red was ineffective. Pigmentation of detached corollas exposed to light was inhibited by the photosynthetic inhibitor 3-(4-dichlorophenyl)-1,1-dimethylurea (DCMU). The chloroplast uncoupler NH₄Cl did not affect anthocyanin synthesis, which was, however, inhibited by the blocking of ATP synthesis in both the chloroplast and the mitochondria by dicyclohexylcarbodiimide (DCCD). Sucrose uptake in vitro was inhibited by DCMU and by darkness, and was promoted equally by blue and red light. The activity of phenylalanine ammonialyase (EC 4.3.1.5) was inhibited in detached corollas grown in the dark or in the light in the presence of DCMU. The activity of chalcone isomerase (EC 5.5.1.6) was not affected by light. These findings suggest that at least two different light reactions are involved in the regulation of anthocyanin synthesis in petunia corollas, namely the high irradiance reaction (HIR) and photosynthesis.     

Involvement of ethylene in the abscission of flowers and petals of Leptospermum scoparium

The growth of cotyledons and primary leaves of I-day-old Sinapis alba L. plants were studied under various light conditions and action spectra produced. For both responses blue and red light are most effective and a strong fluence rate dependency can be observed. The red light effect appears to be mediated through phytochrome, that of blue light being due to a separate blue light receptor, although this receptor requires the presence of far-red absorbing phytochrome (P_fr) in order to be effective.     

Phytochrome-mediated changes in the membrane potential of subepidermal cells of Lemna paucicostata 6746

Light-stimulated transmembrane potential changes have been measured continuously after implantation of microelectrodes into subepidermal cells of the short-day plant Lemna paucicostata 6746. Irradiation for 5 min with white or red light caused a transient hyperpolarization. These potential changes could be suppressed with 10^-6 M DCMU. Irradiation of DCMU-inhibited plants with far-red light for 5 min hyperpolarized the membrane potential, which thereafter was not changed by further far-red application. Consecutive red light irradiation for 5 min depolarized the membrane potential. The red/far-red reversibility of the potential changes (which could be repeated several times with a single plant) suggests the participation of phytochrome.Abbreviations EDTA ethylenediaminetetraacetate - DCMU 3-(3,4-dichlorophenyl)-1,1-dimethyl urea - P_r, (P_fr) red- (far-red-) absorbing form of phytochrome     

Leaf expansion in sunflower as influenced by salinity and short-term changes in carbon fixation

Abstract With a view to defining factors regulating the growth responses of sunflower to salinity, plants were grown in solution culture (0, 50 or 100 mol m⁻³ NaCl) and under natural light, and the areas of every leaf measured once or twice daily from 22 until 38 d after germination. During this period, carbon availability for growth was manipulated by changing light levels and by the use of a photosynthesis inhibitor, DCMU. Salinity reduced relative leaf expansion rates per plant (RLER) by an average of 0.04 (50 mol m⁻³) and 0.08 (100 mol m⁻³) m² m⁻² d⁻¹ compared with control plants of equivalent leaf area: the effects were found in expanding leaves regardless of age or size. Control plants expanded faster during the day than the night, but plants grown in salt had an almost constant RLER throughout the 24 h, indicating that salt influences the rate of utilization of assimilates independently of their production. DCMU reduced RLER considerably in both control and salt-treated plants and reduced the advantage of control plants during the day. Conditions of low light also reduced the differences in RLER between control and salt-treated plants. When salt was removed from the root medium of non-DCMU plants, the expansion rates equalled that of the controls within 24 h and remained at the same levels for the following 3 d measurement period: this recovery applied to leaves of all ages. Salt-grown plants with no photosynthesis (DCMU treatments) also increased their expansion rates upon removal of salt from the root medium, thus providing further evidence that growth was not limited by carbohydrate status, i.e. that salt influences growth primarily via its effects on the rate of utilization of stored assimilates.     

Photoinduction of Spore Germination in Marchantia polymorpha L. is Mediated by Photosynthesis

The effects of light on spore germination (protrusion of protonemata)in the liverwort Marchantia polymorpha L. were examined. Sporegermination was found to be light dependent and light irradiationfor 10 h or longer was necessary. Test using specific wavelengthsshowed that the entire spectrum from near UV to red light waseffective, red light being the most effective. Spore germinationcould be induced by intermittent irradiation with 15-min redlight pulses given every 1 or 2 h for 24 h. The effect of intermittentred light was not reversed by subsequent or simultaneous far-redlight irradiation. However, spore germination was inhibitedby the photosynthesis inhibitor DCMU (100 µM). Completeinhibition of spore germination was found when DCMU was givenduring the light period. When DCMU was applied during the darkperiods, only a slight reduction of germination rate was observed.Further, it was found that Chl formed in the spores during imbibitionin darkness. Light sensitivity increased at nearly the samerate as the appearance of Chl. Moreover, spore germination wasinduced in total darkness by the addition of glucose to themedium. These results clearly indicate that photosynthesis mediatesthe photoinduction of spore germination in Marchantia polymorpha. (Received May 13, 1999; Accepted July 14, 1999)     

Far-Red Light Reflection from Green Leaves and Effects on Phytochrome-Mediated Assimilate Partitioning under Field Conditions

The influence of plant spacing and row orientation on spectral distribution of light received by growing soybean (Gylcine max [L.] Merr.) plants was measured under field conditions. Light absorption, reflection and transmission of individual leaves showed that most of the blue and red was absorbed while most of the far-red was either reflected or transmitted. Plants growing in the field received different ratios of far-red relative to red, depending on nearness and/or orientation of other vegetation. Plants grown in close-spaced rows, or high population densities, received higher far-red/red ratios than did those grown in wide rows, or sparse populations. Heliotropic movements of the leaves also contributed to the far-red reflection patterns associated with row orientation. Under field conditions, differences in far-red/red ratios associated with nearness of competing vegetation became more pronounced with low solar angle near the end of the day. Plants exposed to far-red for 5 minutes at the end of each day in controlled environments, and those grown in close-spaced rows in the field, developed longer internodes and fewer branches. Red, far-red photoreversibility in the controlled environment study indicated involvement of phytochrome. Dry matter partitioning among plant components in the field was related to far-red/red light ratio received during growth and development.     

Genetic analysis of the roles of phytochromes A and B1 in the reversed gravitropic response of the lz-2 tomato mutant

The lz-2 mutation in tomato ( Lycopersicon esculentum ) causes conditional reversal of shoot gravitropism by light. This response is mediated by phytochrome. To further elicit the mechanism by which phytochrome regulates the lz-2 phenotype, phytochrome-deficient lz-2 plants were generated. Introduction of au alleles, which severely block chromophore biosynthesis, eliminated the reversal of hypocotyl gravitropism in continuous red and far-red light. The fri ¹ and tri ¹ alleles were introduced to specifically deplete phytochromes A and B1, respectively. In dark-grown seedlings, phytochrome A was necessary for response to high-irradiance far-red light, a complete response to low fluence red light, and also mediated the effects of blue light in a far-red reversible manner. Loss of phytochrome B1 alone did not significantly affect the behaviour of lz-2 plants under any light treatment tested. However, dark-grown lz-2 plants lacking both phytochrome A and B1 exhibited reduced responses to continuous red and were less responsive to low fluence red light and high fluence blue light than plants that were deficient for phytochrome A alone. In high light, full spectrum greenhouse conditions, lz-2 plants grew downward regardless of the phytochrome deficiency. These results indicate that phytochromes A and B1 play significant roles in mediating the lz-2 phenotype and that at least one additional phytochrome is involved in reversing shoot gravitropism in this mutant.     

光强因子对少花桂幼苗形态和生理指标及精油含量的影响

光是影响植物生长的重要因子之一。它不仅能够影响植物的光合作用,同时,光还以环境信号的形式作用于植物,通过光敏色素等作用途径调节植物生长、发育和形态建成,使植物更好地适应外界环境。除此之外,光还可以影响植物的初生代谢过程和次生代谢。因此提高植物体内重要次生代谢产物,光的因素不可忽视。少花桂(Cinnamomum pauciflorum)是樟科樟属多年生常绿小乔木,其体内含有精油,鲜叶含油量可达3．5％,比黄樟树根含油量高出1倍左右,精油中黄樟油素纯度高达95％以上。以少花桂为材料,采用人工模拟不同生境的光照条件,探讨光强因子对少花桂生长及精油含量的影响,以求对其生产提供理论指导。通过窗纱遮荫实现对其生境光的控制,研究了光强因子对少花桂幼苗形态结构、水分状况、光合指标、生物量、香桂油含量和纯度的影响。结果表明：随生境相对光照强度的减弱,叶片厚度、叶片上表皮厚度、下表皮厚度、栅栏组织、海绵组织厚度、根冠比等都呈现降低的趋势;而平均单叶面积却呈现出增加的趋势;株叶面积在61．5％的全光照下有所增加,而在33．8％和15．4％全光照条件下大幅度减小;遮荫条件下生长的少花桂幼苗根系相对不发达,根冠比小;生境的光照强度会影响植株的水分蒸腾,从而影响含水量。在同样光照下,全光照条件下生长的少花桂幼苗保水能力最强,其次是61．5％全光照,最差的是15．4％全光照。少花桂幼苗的光饱和点、光补偿点随生境中的光强减弱而降低。过度遮荫条件下生长的少花桂幼苗CO2补偿点明显高于自然条件下生长的少花桂幼苗;随生境中的光强度的减弱其光呼吸速率升高,单位叶面积的叶绿素含量增加．Chla／Chlb值减小。遮荫处理后,不同光照条件下生长的少花桂幼苗的质量增加存在显著差异。遮荫过程中61．5％、33．8％和15．4％全光照条件下生长的少花桂幼苗叶片鲜质量的增长速率分别为全光照的1．6倍、1．2倍和0．77倍。香桂油含量以61．5％和33．8％全光照为多,均比全光照高出5％左右,而15．4％全光照叶片含油量又较全光照少5％左右。香桂油中黄樟油素纯度,以33．8％、15．4％全光照生境下的少花桂幼苗叶片为高。少花桂幼苗轻微遮荫(61．5％全光照)栽培．能获得较高的枝叶产量和香桂油产率．重度遮荫(33．8％、15．4％全光照)能获得纯度较高的黄樟油素。     

Phytochromabhängige Veränderungen des Wachstums und der Ionenaufnahme etiolierter Erbsenkeimlinge

Summary Inhibition of internodial growth of pea seedlings by light is compensated for by increased growth of leaves. At a given time the sum of fresh weight of internodes plus the product of fresh weight of leaves times a certain factor is constant in darkness or with different periods of light. This correlation may reflect a competition of internodes and leaves for materials delivered at a lightindependent rate from the cotyledons. This hypothesis was tested by immersing roots of pea seedlings into ⁸⁶Rb labelled K-solutions for one day in darkness, removing the plants from the solutions, exposing the seedlings to near or far red light and measuring the radioactivity and fresh weights of leaves and internodes separately. Radioactivity and fresh-weight were both dependent on phytochrome; i.e. inhibition of ion uptake and of growth in internodes and promotion of both processes in leaves by near red light as compared to dark or far red controls are mediated by phytochrome.Short time experiments of ion uptake by the roots show that K transport into the shoot organs is promoted by light after a lag phase of somewhat more than one hour. This interval corresponds well to the lag phase of the light induced growth inhibition of internodes.Seedlings deprived of cotyledons and roots grow well in water but exhibit no difference in growth rate of leaves and internodes in light and darkness. Light dependence is restored if the seedlings are submersed in approximately 3% sucrose solutions. This result seems to indicate that the influence of light on growth rates of leaves and internodes is dependent on the uptake of material by the cell. It seems possible that in the etiolated pea seedling light promotes growth of leaves by promoting uptake and hampers growth of internodes by inhibiting uptake of essential growth material delivered from the cotyledons.