Phototropic Response Research Articles

Arabidopsis NPH1: a flavoprotein with the properties of a photoreceptor for phototropism.

The NPH1 gene of Arabidopsis thaliana encodes a 120-kilodalton serine-threonine protein kinase hypothesized to function as a photoreceptor for phototropism. When expressed in insect cells, the NPH1 protein is phosphorylated in response to blue light irradiation. The biochemical and photochemical properties of the photosensitive protein reflect those of the native protein in microsomal membranes. Recombinant NPH1 noncovalently binds flavin mononucleotide, a likely chromophore for light-dependent autophosphorylation. The fluorescence excitation spectrum of the recombinant protein is similar to the action spectrum for phototropism, consistent with the conclusion that NPH1 is an autophosphorylating flavoprotein photoreceptor mediating phototropic responses in higher plants.

Cryptochrome blue-light photoreceptors of Arabidopsis implicated in phototropism.

Phototropism-bending towards the light-is one of the best known plant tropic responses. Despite being reported by Darwin and others over a century ago to be specifically under the control of blue light, the photoreceptors mediating phototropism have remained unknown. We have characterized a blue-light photoreceptor from Arabidopsis, named CRY1 for cryptochrome 1; this photoreceptor is a flavoprotein that mediates numerous blue-light-dependent responses. In Arabidopsis, HY4 (the gene encoding CRY1) is a member of a small gene family that also encodes a related photoreceptor, CRY2, which shares considerable functional overlap with CRY1. Here we report that mutant plants lacking both the CRY1 and the CRY2 blue-light photoreceptors are deficient in the phototropic response. Transgenic Arabidopsis plants overexpressing CRY1 or CRY2 show enhanced phototropic curvature. We conclude that cryptochrome is one of the photoreceptors mediating phototropism in plants.

Light Regulation of Phytochrome Content in Wild‐type and Aphototropic Mutants of the Moss Ceratodon purpureus

ABSTRACTIn filaments of the moss Ceratodon purpureus, phototropism is controlled by the photoreceptor phytochrome. Thirty‐three aphototropic mutants with a proposed defect in phytochrome‐chromophore biosynthesis were isolated and analyzed. The phototropic response of those mutants was rescued with the precursor of the phytochrome chromophore, biliverdin. Phytochrome spectral activity was measured in 19 arbitrarily chosen mutants. All contained low but still measurable quantities of photoactive phytochrome; the highest level was around 15% of the wild‐type. The level of total phytochrome (apophytochrome and holophytochrome) as assayed by immunoblotting was indistinguishable from wild‐type. The content of photoactive phytochrome in Ceratodon is light‐regulated. Phytochrome of wild‐type kept for 24 h in red light was reduced to 50% as compared to dark controls but was unaffected by blue. The red‐light‐induced decrease was partially reversible by far‐red light, indicating that phytochrome itself is the photoreceptor for this response. This regulation was further analyzed with the mutant ptr114, which contains 15% photoactive phytochrome as compared to the wild‐type. In this mutant, continuous red light given for 6 days decreased the level of spectrally active phytochrome down to 25% of dark controls, whereas the amount of phytochrome found on immunoblots was hardly reduced. This indicates that the loss of phytochrome affects only the holoprotein and implies that Ceratodon phytochrome is specifically degraded as a far‐red‐absorbing phytochrome.

Light regulation of phytochrome content in wild-type and aphototropic mutants of the moss Ceratodon purpureus.

In filaments of the moss Ceratodon purpureus, phototropism is controlled by the photoreceptor phytochrome. Thirty-three aphototropic mutants with a proposed defect in phytochrome-chromophore biosynthesis were isolated and analyzed. The phototropic response of those mutants was rescued with the precursor of the phytochrome chromophore, biliverdin. Phytochrome spectral activity was measured in 19 arbitrarily chosen mutants. All contained low but still measurable quantities of photoactive phytochrome; the highest level was around 15% of the wild-type. The level of total phytochrome (apophytochrome and holophytochrome) as assayed by immunoblotting was indistinguishable from wild-type. The content of photoactive phytochrome in Ceratodon is light-regulated. Phytochrome of wild-type kept for 24 h in red light was reduced to 50% as compared to dark controls but was unaffected by blue. The red-light-induced decrease was partially reversible by far-red light, indicating that phytochrome itself is the photoreceptor for this response. This regulation was further analyzed with the mutant ptr114, which contains 15% photoactive phytochrome as compared to the wild-type. In this mutant, continuous red light given for 6 days decreased the level of spectrally active phytochrome down to 25% of dark controls, whereas the amount of phytochrome found on immunoblots was hardly reduced. This indicates that the loss of phytochrome affects only the holoprotein and implies that Ceratodon phytochrome is specifically degraded as a far-red-absorbing phytochrome.

Asymmetric, blue light-dependent phosphorylation of a 116-kilodalton plasma membrane protein can be correlated with the first- and second-positive phototropic curvature of oat coleoptiles.

The possible correlation between blue light-dependent phosphorylation of a 116-kD protein and phototropic responses of etiolated oat (Avena sativa L.) seedlings was tested by a micromethod for protein phosphorylation. Quantitation of the basipetal distribution of this protein showed that the in vitro 32p phosphorylation values declined exponentially from tip to node, with more than 50% of the total label being found in the uppermost 5 mm. Nonsaturating preirradiation of the coleoptiles in vivo resulted in partial phosphorylation with endogenous ATP. Subsequent in vitro phosphorylation under saturating irradiation allowed the determination of the degree of in vivo phosphorylation. Unilateral preirradiation resulted in higher in vivo phosphorylation on the irradiated than on the shaded side of the coleoptile. The fluence-response curve for the difference in phosphorylation between both sides of the coleoptile resembles the fluence-response curve for first-positive phototropic curvature, although it is shifted by two orders of magnitude to higher fluences. Possible reasons for this shift are discussed. In the coleoptile base the phosphorylation gradient across the coleoptile becomes larger with increasing time of irradiation at a constant fluence. Thus, phosphorylation of the 116-kD protein, in accordance with second-positive phototropic curvature, does not obey the Bunsen-Roscoe reciprocity law.

Restoration of phototropic responsiveness in decapitated maize coleoptiles.

The literature indicates that the tip of maize (Zea mays L.) coleoptiles has the localized functions of producing auxin for growth and perceiving unilateral light stimuli and translocating auxin laterally for phototropism. There is evidence that the auxinproducing function of the tip is restored in decapitated coleoptiles. We examined whether the functions for phototropism are also restored by using blue-light conditions that induced a first pulse-induced positive phototropism (fPIPP) and a time-dependent phototropism (TDP). When the apical 5 mm, in which photosensing predominantly takes place, was removed, no detectable fPIPP occurred even if indole-3-acetic acid (lanolin mixture) was applied to the cut end. However, when the blue-light stimulation was delayed after decapitation, fPIPP became inducible in the coleoptile stumps supplied with indole-3-acetic-acid/lanolin (0.01 mg g-1), indicating that phototropic responsiveness was restored. This restoration progressed 1 to 2 h after decapitation, and the curvature response became comparable to that of intact coleoptiles. The results for TDP were qualitatively similar, but some quantitative differences were observed. It appeared that the overall TDP was based on a major photosensing mechanism specific to the tip and on at least one additional mechanism not specific to the tip, and that the tip-specific TDP was restored in decapitated coleoptiles with kinetics similar to that for fPIPP. It is suggested that the photoreceptor system, which accounts for fPIPP and a substantial part of TDP, is regenerated in decapitated coleoptiles, perhaps together with the mechanism for lateral auxin translocation.

Phytochrome‐mediated Phototropism in Adiantum Protonemata II. Participation of Phytochrome Dark Reversion

ABSTRACTA microbeam irradiation technique was used to analyze phytochrome‐mediated phototropism of the protonema of the fern Adiantum capillus‐veneris. One side of the sub‐apical zone of a dark‐adapted protonema was irradiated with a red‐light (R) microbeam to induce phototropic curvature toward the irradiated side. Except the cases where fluence‐response relationships were examined, the protonema was stimulated with the microbeam for about 30 s to provide a fluence (5.3–5.5 mmol m‐2) optimal for curvature. When the whole protonema was pretreated with a high fluence of R (about 9 mmol m‐2), no significant curvature could be induced by immediately subsequent one‐sided microbeam stimulation. It was found, however, that curvature became inducible progressively as the time of microbeam stimulation was delayed after the R pretreatment. The protonema gained nearly full responsiveness within 40 min after the pretreatment. Moreover, the inductive effect of microbeam R escaped rapidly from the reversing effect of far‐red light. These results indicated that most of the far‐red‐absorbing form of phytochrome (Pfr), which mediates the phototropic response, undergoes relatively fast dark reversion to the red‐absorbing form. The dark reversion kinetics was analyzed further by taking into account that the phototropic responsiveness after the R pretreatment was measured in the presence of background Pfr over the protonema. This analysis revealed a rate constant of about 0.002 s‐1 (t1/2˜ 6 min) for the dark reversion. It is considered that the Pfr dark reversion plays a role in establishing a lateral Pfr gradient in the unilaterally irradiated protonema.

The function of phytochrome A

ABSTRACTKnowledge of the photoperceptive function of phytochrome A has improved substantially thanks to the availability of mutants lacking phytochrome A and transgenic plants transformed with the PHYA gene in sense or anti‐sense orientation. In imbibed seeds, phytochrome A mediates very‐low‐fluence responses. In etiolated seedlings, phytochrome A mediates very‐low‐fluence responses, high‐irradiance responses under continuous far‐red light, responsivity amplification to phytochrome B and red‐light enhancement of the phototropic response to blue light. In light‐grown seedings, phytochrome A modulates the extent of response to reductions in red/far‐red ratio perceived by phytochrome B, perceives daylength extensions and night interruptions affecting flowering, and perceives light treatments resetting endogenous rhythms. Under natural radiation these abilities are manifested during seed germination and seedling de‐etiolation under dense canopies or extremely low light fluences, and during early neighbour detection, but other processes await experimental evaluation. Phytochrome A affects growth and development throughout the whole life cycle of angiosperms.

Phototropic Response of the Bean Pulvinus: Movement of Water and Ions

Abstract:Segmental analysis of the laminar pulvinus of Phaseolus vulgaris L. showed that its phototropic curvature is accompanied by efflux of inorganic ions and water from its contracting sector and a comparable influx into its expanding one. All the major ions, except Na+, contributed to this transport, suggesting that the response to light involves changes in the driving force, or conductivity of a wide range of solutes. During the curvature, K+ and CI− made the greatest and equivalent contributions to efflux, but only Cl− exhibited a matching influx into the expanding sector, while K+ influx was much less. Use of the cell pressure probe showed that, as the laminar angle of elevation changed between −40° to +40°, turgor pressure in the expanding motor cells increased by 0.48 MPa and decreased in the contracting cells by 0.32 MPa. Picoliter osmometry of single‐cell samples showed that during this movement vacuolar osmotic pressure remained constant. Thus, changes in turgor pressure resulted from changes in apoplastic, rather than the protoplastic osmotic pressure. Volumetric modulus of elasticity of pulvinar motor cells is very low, showing that their walls are very elastic. These properties increase the effectiveness of converting osmotic work into the large‐scale, reversible volume changes responsible for leaf movements.

Influence of phototropic response of spore germ tubes on infection process in Colletotrichum lagenarium and Bipolaris oryzae

The germ tubes ofColletotrichum lagenarium showed negative phototropism to UV-blue (300–520 nm) and far-red (>700 nm) regions with maximum in the near ultraviolet (NUV) region, while monochromatic radiations of 575–700 nm (yellow-red region) induced positive phototropism with maximum in the red region. Green light (520–575 nm) was ineffective. Negative phototropism-inducing wavelength regions inhibited germ tube growth and positive phototropism-inducing wavelength regions promoted it significantly.Bipolaris oryzae did not show any phototropic response and light did not affect the germ tube growth. These results indicate that the lens effect, in combination with the light growth reaction and light growth inhibition, is the mechanism of the phototropism of germ tubes ofC. lagenarium. NUV radiation, which induced negative phototropism ofC. lagenarium, promoted appressorium formation, while red light, which induced positive phototropism, suppressed it significantly. In the case ofB. oryzae, light did not affect the infection structure formation. These results indicate that negative phototropism of germ tubes ofC. lagenarium favors the infection process by facilitating the contact of the tips of germ tubes with the host surface, while positive phototropism has the opposite effect.

Mutations of Arabidopsis in potential transduction and response components of the phototropic signaling pathway.

Four genetic loci were recently identified by mutations that affect phototropism in Arabidopsis thaliana (L.) Heyhn. seedlings. It was hypothesized that one of these loci, NPH1, encodes the apoprotein for a phototropic photoreceptor. All of the alleles at the other three mutant loci (nph2, nph3, and nph4) contained wild-type levels of the putative NPH1 protein and exhibited normal blue-light-dependent phosphorylation of the NPH1 protein. This indicated that the NPH2, NPH3, and NPH4 proteins likely function downstream of NPH1 photoactivation. We show here that, although the nph2, nph3, and nph4 mutants are all altered with respect to their phototropic responses, only the nph4 mutants are also altered in their gravitropic responsiveness. Thus, NPH2 and NPH3 appear to act as signal carriers in a phototropism-specific pathway, whereas NPH4 is required for both phototropism and gravitropism and thus may function directly in the differential growth response. Despite their altered phototropic responses in blue and green light as etiolated seedlings, the nph2 and nph4 mutants exhibited less dramatic mutant phenotypes as de-etiolated seedlings and when etiolated seedlings were irradiated with unilateral ultraviolet-A (UV-A) light. Examination of the phototropic responses of a mutant deficient in biologically active phytochromes, hy1-100, indicated that phytochrome transformation by UV-A light mediates an increase in phototropic responsiveness, accounting for the greater phototropic curvature of the nph2 and nph4 mutants to UV-A light than to blue light.

Structural basis for the red light induced repolarization of tip growth in caulonema cells ofCeratodon purpureus

Two dynamic changes are associated with the phytochrome-regulated phototropic response in tip cells of the mossCeratodon purpureus: a tip-located gradient shift of chlortetracy-cline (CTC)-stained calcium and a structural reorganization of apical microfilaments (MFs). We examined the interdependence of these processes. Cells were treated with the antimicrotubule drug oryzalin, the antimicrofilament drug cytochalasin-D, and the calcium channel blocker nifedipine. respectively. The effects on phototropic growth, on the structural alignment of the cytoskeleton (microtubules, MTs; microfilaments) and on the distribution of CTC-stained calcium were studied under each of these conditions. In gravitropically growing tip cells the apical MFs form a cortical collar-like structure, consisting of actin bundles with a parallel axial alignment. These MFs point towards the presumptive growing point, a weakly stained region in the tip of the cell from which bundles are absent. MTs are present in the cortex and in the endoplasm of the tip, predominantly oriented longitudinally. The MTs converge within the central apex. The cells show a steep tip-to-base CTC-calcium gradient with its highest signal in the central apex. Destruction of MTs by 1 μM oryzalin induces several translocational effects: (i) the growing zone and phototropic outgrowth shift from the apex to subapical parts of the cell; (ii) the structural integrity of the apical MFs and the tip-to-base alignment of the CTC-calcium gradient are disturbed; and (iii) the red light induced gradient shift and the reorientation of MFs proceed in an expanded area spanning from the tip to subapical parts of the cell. Cytochalasin-D (10 μg/ml) destroys the MFs. Under these conditions tip growth stops and the phototropic outgrowth is suppressed. The apical MT-structure and the CTC-calcium gradient are not influenced by the agent. Unilateral red light still induces the light-directed translocation of the gradient. Tip cells “memorize” a unilateral irradiation applied during growth inhibition with cytochalasin-D. After recovery in darkness the cells start to grow in the former light direction. The restoration of the MFs precedes the outgrowth. The structural alignment of the rebuilt actin bundles indicates the future growth direction. The calcium channel blocker nifedipine (10 βM) also inhibits tip growth and concurrently phototropic outgrowth. Nifedipine destroys the CTC-calcium gradient and apical MFs; MTs are not influenced by the channel blocker.

Light-driven movements of the trifoliate leaves of bean ( Phaseolus vulgaris L.). Spectral and functional analysis

Summary The light-driven responses of the terminal leaflet of bean were analyzed spectrally and functionally. Laminar elevation increases rapidly in response to continuous overhead exposure of its pulvinus to blue light. This response is enhanced in its early stages by simultaneous exposure to red light. The pulvinus responds similarly to continuous overhead unmixed red, or far-red light, albeit at much lower rates. The response to overhead red, alone, or during enhancement of the response to blue, was not affected by simultaneous far-red. However, the response to blue alone, or enhanced by mixture with red, was partially inhibited by simultaneous exposure to far-red. The results suggest that the response to blue resulted mostly from a blue-absorbing pigment system, but may involve some absorption by phytochrome, while responses to red or far-red, with and without blue, may be mediated by high-irradiance responses of phytochrome. Functional differences between the responses to red and blue become apparent when the abaxial (lower), or lateral sectors of the pulvinus are exposed to them, separately and in combination. These differences suggest that red controls the photonastic unfolding of the pulvinus, whereas blue controls its phototropic responses. These responses co-exist in the same tissue, but are separate and additive.

Light signaling in plants

Abstract Light signals have profound morphogenic effects on plant development. Signals perceived by the red/far‐red absorbing phytochrome family of photoreceptors and the blue/green/ UV‐A absorbing cryptochrome photoreceptor converge on a group of pleiotropic gene products defined by the COP/DET loci to control the pattern of development. The signaling pathway, although still undefined, includes several classic signaling molecules, such as G‐proteins, calcium, calmodulin, and cGMP. A separate signaling pathway is involved in the modulation of the phototropic response. Additional mutants have been identified that affect subsets of light signaling responses. This review provides an overview of our current understanding of the light signaling process, in particular recent genetic and biochemical advances.

How Plants Find Light in Patchy Canopies. A Comparison between Wild-Type and Phytochrome-B-Deficient Mutant Plants of Cucumber

We address the following questions : (a) do plants that colonize horizontally-patchy environments preferentially project leaf area into light gaps and avoid poorly illuminated sites ? (b) is this 'foraging' ability impaired in plants that lack phytochrome B, one of the plants' information-acquiring photoreceptors ? We used cucumber (Cucumis sativus L.) plants as test material and our approach was based on studies of the dynamics of gap colonization by wild-type (WT) and lh-mutant plants. The lh mutant lacks phytochrome B but has WT levels of phytochrome A. When de-etiolated, lh seedlings show reduced or no response to alterations of the red (R) to far-red (FR) ratio of the incident light, one of the environmental factors that plants use to monitor the proximity of other plants. Controlled-environment experiments showed that seedlings of both genotypes are able to sense irradiance gradients and actively project nodes towards light gaps via phototropic (stem-bending) responses. A mechanism independent of phytochrome B also appeared to control the angle of display of individual leaves with respect to the direction of illumination. However, when compared over periods of several weeks, WT plants were far more efficient than lh mutants at invading light gaps. Thus, WT plants grown in the field for 4 weeks at the edges of an experimental maize canopy projected outside the canopy nearly all the nodes produced. In contrast, ∼50% of the nodes and more than 80% of the apical buds of lh mutant plants were deployed under the maize canopy. The lower ability of the phytochrome B-deficient lh mutant to 'forage' for light, compared with WT plants, appears to be the integrated product of a lower capacity to locate light gaps (owing to the lack of R :FR-driven phototropism) and a lower capacity to retain modules into high-light patches. In relation to the latter, lh shoots exposed to high R :FR ratios (simulated gap-light) retain a phenotype characterized by long inter-nodes and high apical dominance, two features that would increase the likelihood of exiting light gaps. We show that shoots of mature WT plants grown under high R :FR ratio are diagravitropic, whereas lh shoots are orthogravitropic. The diagravitropic habit, coupled with an efficient phototropic system, appears to help WT shoots to escape from the shaded sectors and invade light gaps. Compared with lh plants, WT plants grown under high R :FR have delayed tendril production and reduced stem-bending responses to mechanical stress exerted by tendrils. These two factors combine with the ones listed above to cause the direction of shoot spreading in WT plants to be dictated mainly by the spatial distribution of light gaps and not by the distribution of potential points of support for tendril attachment.

Nastic curvatures of wheat coleoptiles that develop in true microgravity.

Dark-grown wheat coleoptiles developed strong curvatures within 5 h of being transferred in orbit from a 1 g centrifuge to microgravity during an experiment flown on the IML-1 shuttle mission. The curving tendency was strongest in seedlings that were immature, with coleoptiles shorter than 10 mm at the time of transfer. The curvature direction was non-random, and directed away from the caryopsis (the coleptile face adjacent to the caryopsis becoming convex). The curvatures were most marked in the basal third of the coleoptiles, contrasting with phototropic responses, which occur in the apical third. We interpret these curvatures as being nastic, and related to the curvatures commonly reported to occur during clinostat rotation treatments.

Mutations in the NPH1 locus of Arabidopsis disrupt the perception of phototropic stimuli.

The phototropic response is an important component of seedling establishment in higher plants because it orients the young seedlings for maximal photosynthetic light capture. Despite their obvious importance, little is known about the mechanisms underlying the perception and transduction of the light signals that induce phototropic curvatures. Here, we report the isolation of eight mutants of Arabidopsis that lack or have severely impaired phototropic responses. These nph (for nonphototropic hypocotyl) mutants comprise four genetic loci: nph1, nph2, nph3, and nph4. Physiological and biochemical characterization of the nph1 allele series indicated that the NPH1 locus may encode the apoprotein for a dual-chromophoric or multichromophoric holoprotein photoreceptor capable of absorbing UV-A, blue, and green light and that this photoreceptor regulates all the phototropic responses of Arabidopsis. It appears that the NPH1 protein is most likely a 120-kD plasma membrane-associated phosphoprotein because all of the nph1 mutations negatively affected the abundance of this protein. In addition, the putative NPH1 photoreceptor protein is genetically and biochemically distinct from the HY4 protein, which most likely acts as a photoreceptor for blue light-mediated hypocotyl growth inhibition. Furthermore, the NPH1 and HY4 proteins are not functionally redundant because mutations in either gene alone affect only one physiological response but not the other, thus providing strong support for the hypothesis that more than one blue light photoreceptor is required for the normal growth and development of a seedling.

Reorganization of microfilaments in protonemal tip cells of the moss Ceratodon purpureus during the phototropic response.

The F-actin distribution in caulonemal tip cells of the moss Ceratodon purpureus was examined by rhodamine-phalloidin staining. Gravitropically-growing caulonemal tip cells of the moss possess a distinct alignment of microfilaments (MFs) in their apices. Axially oriented actin bundles run from subapical regions to the apex where they converge towards a central area of the tip, although bundles are absent from the central area itself thus forming a collar-like structure. During a unilateral red light irradiation the actin strands of the apical dome become reoriented towards the irradiated apical flank and still surround an area free of MFs, the point of prospective outgrowth. This process is closely correlated with the morphological effect of bulging and precedes the light-directed outgrowth. The collar structure is essential for the tubular growth form. In darkness, under the influence of antimicrotubule agents the structure is decomposed, the actin strands drift along the cell flanks and finally accumulate in randomly distributed areas where further growth takes place. The microtubules (MTs) are not involved in the phytochrome-mediated reorientation of the microfilaments. Unilateral red light suppresses the distorting effect of antimicrotubule drugs and restores the collar structure with a pronounced light-directed orientation. Instead, the MTs seem to be responsible for restricting the reorientation to the cell tip. This notion is based on the observation that the small area in the apical dome, which is normally the exclusive location of the light-regulated MF rearrangement, extends towards the cell base when MT inhibitors are applied before the unilateral red light irradiation. This in turn leads to a non-tubular expansion of the light-directed cell flank.

The phototropic response of Triticum aestivum coleoptiles under conditions of low gravity

ABSTRACTWheat (Triticum aestivum L. cv Broom) coleoptiles were stimulated by unilateral blue light pulses, the duration of which varied between 3 s and 30 min, under microgravity conditions on the IML‐1 Spacelab mission and in ground controls. The stimuli covered first positive, indifferent and second positive response regions. When phototropic responses were observed under low‐gravity conditions, slightly fewer seedlings responded compared with 1 g conditions. The latent period was similar in flight and 1g treatments (10–20 min), except for the response to 300,μmol m−2 in the indifferent response region, where a positive response in flight plants followed a 130 min latent period, while no response was observed in 1 g plants. First positive responses at Og were slightly enhanced, both in magnitude and in duration, compared to the 1 g controls, but not to the extent predicted by clinostat studies. The response kinetics in the second positive region at 1g showed a plateau at 120 min, in contrast to the single maximum at Og. The fluence‐response relationship was similar in both flight and ground controls. Only the responses to 4 and 6μmolm‐2 showed significantly greater curvatures at 9g. This contrasts with previous clinostat studies, which reported substantial response enhancement at all fluence levels.

Negative phototropism in young gametophytes of the fern Schizaea pusilla

ABSTRACT Schizaea pusilla is a rare fern that occurs in acidic bogs and is one of the few fern species that maintains a filamentous gametophyte throughout its development. To expand our knowledge of the physiology of this fern, phototropic responses were examined in young gametophytes. In contrast to germ filaments of other fern species, apical protonemata of young gametophytes are negatively phototropic in continuous white, red and blue light at all fluence rates tested. The expression of phototropic curvature is not limited by time since apical protonemata are also negatively phototropic when they are given brief exposures of light and then placed in the dark. In other lower plant groups such as mosses and some algae, the direction of phototropic curvature can change depending on light quality and intensity, but in young gametophytes of Schizaea, negative phototropic curvature was observed in all conditions studied. Blue light is the most effective in promoting the negative phototropic response in Schizaea.