Fruiting ofLyophyllum tylicolor in plate culture on Soytoneglucose agar and urea-treated soil extract agar

Lyophyllum tylicolor, which forms mycelial basidia (and basidiospores), produced fruit-bodies when cultivated at 20°C under continuous illumination of 400–700 lux on agar plates containing Bacto-Soytone and glucose or an extract from urea-treated soil. Under these conditions, mycelial basidia were also observed on the Soytone-glucose agar, but not on the soil extract agar. In darkness, fruit-bodies and mycelial basidia were not observed on either medium. In culture on the soil extract agar, fruit-body primordia were produced at the position of the margin of the colony when it was transferred from darkness to continuous light; stipes did not elongate under illumination of ca. 2000 lux; and mycelial basidia and basidiospores, but not fruit-bodies, developed when glucose concentration in the medium was as high as 1% (w/v).     

Action Spectra for Stimulatory and Inhibitory Effects of UV and Blue Light on Fruit-Body Formation in Coprinus congregatus

Spectral sensitivity for stimulatory and inhibitory effectsof light on fruit-body formation in Coprinus congregatus wasdetermined between 250 and 730 nm using the Okazaki Large Spectrograph.Eight-day-old dark grown cultures were exposed to varying amountsof monochromatic photon fluences for 60 s. Primordial initiationwas strictly localized in the youngest hyphae of the culture.After a dark period of 24 h at 25C, the primordial initiationwas assayed by counting the number of primordia. The actionspectrum showed peaks of effectiveness at 260, 280, 370 and440 nm. The quantum effectiveness at 280 nm was 4 times higherthan that at 440 nm. The lethal effect of far UV (260–280nm) was demonstrated when using 100 times higher photon fluencesthan that inducing primordial formation. The primordia growing in continuous light required an uninterrupteddark period for 5 h at 25C to produce sporulating fruit-bodies.A brief exposure to light during the dark period inhibited thedevelopment of primordia. The action spectrum for this photoinhibitoryeffect showed maxima at 280, 350, 380, 440 and 460 nm. The quantumeffectiveness at 280 nm was Ca. 1.3 times higher than that ofblue light. The spectral sensitivities for primordial initiationand for inhibition of primordial development were quite similarand suggested a common photoreceptor during fruit-body morphogenesis. ⁴ Permanent address: Botany Department, Faculty of Science,University of Tokyo, Hongo, Tokyo 113, Japan.     

Photoperiodic response of Coprinus congregatus: Effects of light breaks on fruiting

Light initiated fruit-body primordia of Coprinus congregatus Bull, ex Fr. were subjected to different dark periods (4 h to 24 h) and exposed to short blue light pulses at different times. The light break inhibited the development of primordia as did continuous light. The time of maximum sensitivity to a light break was dependent on the duration of the dark period. A short light break imposed two-thirds of the way through the dark period produced strong inhibition of fruiting. The higher the temperature during the dark period, the lower the irradiance required for 50% inhibition of fruiting at the time of maximal sensitivity. During a very long dark period (48 h) a light break was no longer inhibitory. The light break fulfilled the light requirement for normal morphogenesis and defined the time the fruit-bodies sporulated.     

Effect of Ammonia on Fruit-body Induction of Coprinus cinereus in Darkness

Coprinus cinereus produced only vegetative mycelia on a potatodextrose medium at 25°C in darkness. When ammonia waterwas added to 5-day-old cultures on the same medium at the concentrationsof 0.05 to 0.4 g NH₃/liter, primordia formed after 3 days inthe dark. Some ammonium salts causing alkalinity in the mediumwere also effective for fruit-body induction, but non-basicammonium salts were not effective unless sodium hydroxide wasadded to make the medium alkaline. The presence of ammonia at least for 24 hr was enough to induceprimordium formation when 5-day-old colonies, after being washed,were treated with ammonia water and then cultured on fresh mediumor even on distilled water. (Received September 10, 1980; Accepted December 29, 1980)     

Effect of light on the initiation of pileus formation in a basidiomycete, Favolus arcularius

Pileus formation in Favolus arcularius is induced by light,but no photoinduction occurred in young epileate stipes. Thestipes usually had to attain a length of about 5 mm to be photosensitive.Synchronous pileus formation could be induced by exposure tolight using epileate stipes which had been preincubated in darknessfor 48 to 72 hr. The pileus primordium formed about 24 hr afterthe start of illumination, however, continuous illuminationwas not necessary to produce this effect. A dark period givenbetween 1 and 8 hr after the start of illumination did not retardpileus formation. The photoinduction of pileus formation involvedtwo light-requiring processes, one occurring during the firsthour (the first light process) and the other from the 8th tothe 24th hr (the second light process). The photoresponse inthe first light process was saturated with 5 lux of light, buta light intensity below 1 lux was essentially ineffective. Onthe other hand, the reaction in the second light process couldbe started by less than 2 lux, and was accelerated by increasingthe light intensities up to about 150 lux. Further increasesin light intensity did not improve any significant effect. (Received April 30, 1974; )     

The Effect of Temperature on the Initiation of Leaf Primordia in Developing Potato Sprouts

Kirk, W W., Davies, H. V. and Marshall, B. 1985. The effectof temperature on the initiation of leaf primordia in developingpotato sprouts.—J. exp. Bot. 36: 1634–1643. Initiation of leaf primordia in potato sprouted out of soilin light was an asymptotic function of thermal time and thebase temperature for the process was 3.6 °C. The parametervalues of the asymptotic function were universal for cv. MarisPiper. The estimated rate of leaf primordium initiation decreasedlinearly from 0.033 leaf pnmordia (K day)^–1 when abouteight leaf primordia were present to zero after a maximum numberof 24 leaf primordia had been initiated. The decrease in rateof development with increasing number of primordia may be dueto depletion of mother tuber resources. The transition of theapex from a vegetative to a reproductive state was not the factorlimiting the initiation of additional leaf primordia. Key words: Potato, Solanum tuberosum L., leaf primordia initiation, temperature, thermal time, development     

Fruiting in Sphaerobolus with Special Reference to Light

Sphaerobolus grows and, provided there is sufficient illumination,fruits readily on oatmeal agar or on malt agar. No effect oflight on vegetative growth can be demonstrated. On the maltmedium, increased fruiting occurs with increase of nutrientup to 4 per cent, malt, but at higher concentrations fruitingis not increased and may be retarded. A chemically defined mediumwith starch as the carbon source allows fruiting, but at a lowlevel. Temperature has a profound effect on basidiocarp development;above 25 C. no fruit-bodies are normally formed although vegetativegrowth is approximately optimal at that temperature. For overallfruit-body production at 20 C, light above 100 lux is necessaryand light remains a limiting factor up to about 1, 000 lux.Under continuous light of suitable intensity, fruit-bodies continueto develop and discharge glebal-masses for many weeks. Thereis a distinct periodicity of discharge with (at 20 C.) about12 days between peaks of activity. This corresponds with thetime taken for basidiocarp initiation and development. A number of developmental stages of the basidiocarp are recognized.The final stage, glebal-mass discharge from stellately openedfruit-bodies, is indifferent to light, but all other stagesare stimulated by light. The light intensity for effective stimulationfalls during development and for the penultimate stage an intensityas low as 1 lux is effective. Only light of wave-length below500 mµ is active in overall basidiocarp development. Inthe sensitive region between 400 mµ and 500 mµ,there appear to be peaks of sensitivity around 440 mµand 480 mµ. In alternating light and darkness, simulating natural conditions,glebal-mass discharge occurs in the light periods. With a regimenof 24 hours light and 24 hours of darkness discharge is mainlyin the dark periods.     

Isolation and characterization of developmental variants in fruiting using a homokaryotic fruiting strain ofCoprinus cinereus

Developmental variants in fruiting ofCoprinus cinereus were induced by mutagenizing oidia of the homokaryotic fruiting strain CopD5-12 with UV light. Through screening of 2,696 isolates, 1,018 strains exhibited defects in fruiting and were classified into 8 groups: (1) knotless variants, which fail to form hyphal knots, the first visible sign of fruiting; (2) primordiumless variants, which form hyphal knots but fail to develop fruit-body primordia; (3) maturationless variants, which form fruit-body primordia but do not form mature fruit bodies; (4) elongationless variants, which form mature fruit bodies with short stipes; (5) expansionless variants, which form mature fruit bodies with unexpanded pilei; (6) sporeless variants, which fail to produce black basidiospores, resulting in fruit bodies with white pilei after maturation; (7) compound type, which includes variants exhibiting several of the phenotypes described above; (8) others, including variants that produce a “dark stipe” even under in light/dark conditions, which is formed under continuous darkness in the wild-type. Two elongationless variants were characterized histologically.     

Light Breaks and Fruit-Body Maturation in Coprinus congregatus: Dark Inhibitory and Dark Recovery Process

Experiments were conducted to better understand the inhibitoryeffect of lightduring the dark-induced process of fruit-bodysporulation of Coprinus congregatus Bull, ex Fr. Light-initiatedfruit-body primordia were subjected to different dark periodsinterrupted by a short blue light break at different times.The sporulating response depended on the duration of the darkperiod following the light break. For any inductive dark periodlonger than 3.5 h, a period of darkness lasting half as longas the inductive night completely inhibited fruit-body maturationwhen given after the light break (dark inhibitory process).Longer dark periods after the light break causedrecovery ofthe maximal sporulating response (dark recovery process). Theeffects of the dark inhibitory and the dark recovery processwere alternately reversible, the sporulating response dependingon the duration of darkness after the last light break. Studyof the time course of sporulation showed that a new dark-inducedprocess of fruit-body sporulation was initiated by the beginningof the dark period after the light break. (Received August 2, 1982; Accepted May 6, 1983)     

EXPERIMENTAL CONTROL OF FRUIT-BODY FORMATION IN COPRINUS MACRORHIZUS

In order to establish a proper experimental system for studying the physiological and biochemical processes of fruit-body formation in a Basidiomycetes, Coprinus macrorhizus Rea f. microsporus Hongo, various culture conditions, especially light and temperature, were investigated. The use of homogenates of fruit-body primordia, instead of mycelia, as inocula was effective for maintaining cultures capable of active fruit-body formation during many successive cultivations. At least two successive intermittent illuminations every 12 hr during the 3rd and 4th days of incubation were required for the differentiation of pilei. The most effective wave lengths of incident light were found in the region from 440 to 485 mμ. Temperature effects on fruit-body formation were exhibited in two stages of morphogenesis; i.e., in the induction of primordia formation from vegetative hyphae (by 5°-treatment) and in the transition phase from primordia formation to fruit-body development (by 20°-treatment). Based on these observations, three experimental systems for physiological and biochemical studies on the fruit-body formation have been proposed.     

Development of Lateral Root Primordia in Vicia faba, Pisum sativum, Zea mays andPhaseolus vulgaris: Rates of Primordium Formation and Cell Doubling Times

Lateral root primordium development has been examined in primaryroots of Vicia faba L., Pisum sativum L., Zea mays L. and Phaseolusvulgaris L. Following their initiation from an estimated minimumnumber of 77–162, 20–57, 17 and 12 cells respectivelyin Vicia, Phaseolus, Pisum and Zea, the primordia rapidly increasedin cell number to emerge as secondary roots about 2.8–3.6days later depending on the species being examined. Cell doublingtimes were estimated directly from cell numbers at differenttimes following primordium inception and were found to increasewith increase in primordium size in each of the species investigated. The number of primordia formed per cm of root growth per daywas greatest in Zea and least in Pisum. A comparison of thedata obtained for Vicia with that in the literature led to theconclusion that although the number of primordia produced percm of root growth was independent of the rate of primary elongation,the number produced per day increased in a linear fashion withincrease in the rate at which the primary lengthened. Vicia faba L, Pisum sativum L, Zea mays L, Phaseolus vulgaris L, broad bean, garden pea, maize, dwarf bean, root primordia, cell division, cell doubling time     

Light-induced formation of fruit-bodies in a basidiomycete, Favolus arcularius (FR.) AMES

fruit-bodies in Favolus arcularius. The effect of light lastedfor about one day after transfer to darkness. The mycelium became sensitive to light about 2.5 days afterinoculation; i.e., at the beginning of the rapid growth phase.The site of fruiting was 2–5 mm inside the edge of colony(actively dividing zone) at the start of illumination. Whenone half of the plate culture was illuminated, fruiting wasrestricted to the illuminated half of the colony ; i.e., theeffect of light was localized. These results suggest that thecells sensitive to light are the actively dividing cells. Under a fixed light intensity, the total irradiation time requiredfor the initiation of fruiting was nearly constant, irrespectiveof the durations of pre-incubation in darkness and the dailyillumination period. With increasing light intensities, up toabout 500 lux, fruiting was promoted, however, a further increasein light intensity was inhibitory. (Received March 27, 1968; )     

Growth of fruit-bodies inFavolus arcularius

The fruiting ofFavolus arcularius in culture is described. When the cultures, which have been pre-incubated in darkness to allow the inoculum mycelia to become thick and white wooly in texture, are exposed to light, fruit-body primordia, 1 mm in height, are formed about 4 days after the start of illumination. The primordium develops into a cylindrical stipe, the growth of which mainly occurs in the final 1 mm of the terminal region. Hyphal elongation in the region within 3 mm of the apex is predominant in the growth of the pileate stipe. With maturation of the stipe, changes in hyphal orientation occur on the periphery of the subapical region, and then the pileus-primordium is formed. The differentiation into the inner layer and the outer layer (pre-hymenial layer) in the pileus tissue is completed at this stage. The early growth of the pileus may be due to rapid elongation of the hyphae on the margin in addition to gradual expansion of the hyphae in the preformed pseudo-tissue. When the pileus has grown to about 3 mm in diameter, the subsequent three to four fold increase in size may be due to parallel expansion of the hyphae constituting the young pileus tissue.     

Cultural properties of a luminous mushroom,Mycena chlorophos

Cultural conditions on mycelial growth and fruit-body formation ofMycena chlorophos were studied. The optimum temperature of the mycelial growth was 27°C and the optimum initial pH of medium was 4.0. Peptone agar medium was suitable for the spawn culture. Compost medium containing rice bran at 10% (fw/fw) was appropriate for fruitbody formation in the Petri dish. Light was essential for initiation of primordia, and low-temperature treatment induced fruit-body formation effectively. The optimum conditions for fruit-body formation were found to be the cultivation at 27°C for 4 wk and continued cultivation for 3 wk under illumination at an intensity above 0.2 lx and at 21°C after casing with moist compost powder. In the fruit-bodies obtained, the maximum photosensitive wavelength of luminescence was 522 nm and the optimum temperature for emission was 27°C. The luminescence of a fruit-body was observed for about 3 d consecutively at 21°C.     

Hyphal ultrastructure in fruit-body primordia of the basidiomycetesSchizophyllum commune andCoprinus cinereus

Summary Light and electron microscopic investigations of fruit-body primordia of the basidiomycetesSchizophyllum commune andCoprinus cinereus showed that hyphal fusions are common in specific areas of the fruit-body primordia of both species. In these areas conspicuous amounts of a mucilaginous substance occur between the closely packed hyphae. A possible function of this mucilage is to aid the adhesion of hyphae prior to fusion. In the fruit-body primordium ofCoprinus cinereus the dolipore/parenthesome septum is surrounded by an additional hemispherical membranous cap (outer cap). Such a cap was never found inSchizophyllum commune fruit-body primordia.     

The Relationship Between the Distribution of Periclinal Cell Divisions in the Shoot Apex and Leaf Initiation

Periclinal cell divisions in vegetative shoot apices of Pisumand Silene were recorded from serial thin sections by mappingall the periclinal cell walls formed less than one cell cyclepreviously. The distribution of periclinal divisions in theapical domes corresponded to the distributions subsequentlyoccurring in the apices when the young leaf primordia were forming.In Pisum, periclinal divisions were almost entirely absent fromthe I₁ region of the apical dome for half a plastochron justafter the formation of a leaf primordium and appeared, simultaneouslyover the whole of the next potential leaf site, about half aplastochron before the primordium formed. In Silene periclinaldivisions seemed to always present in the apical dome at thepotential leaf sites and also round the sides of the dome wherethe ensheathing leaf bases were to form. Periclinal divisionstherefore anticipated the formation of leaf primordia by occuring,in Pisum about one cell cycle and in Silene two or more cellcycles, before the change in the direction of growth or deformationof the surface associated with primordial initiation. Pisum, Silene, planes of cell division, orientation of cell walls, leaf primordia, shoot apical meristem, plastochron     

Root-to-shoot primordium conversion on Sesbania rostrata Brem. stem explants

The morphogenetic responses of cultured stem explants of Sesbaniarostrata Brem. from various positions along the stem axis wereanalysed after treatment with four growth regulators (BAP, NAA,kinetin, and GAJ. Internodal explants formed adventitious shootbuds when cultured on a Murashige and Skoog basal medium withoutadded growth regulators. Histological studies of regenerated shoot buds revealed thatapproximately 30% of the buds resulted from the conversion ofa preformed root primordium (characteristic of this species)into a shoot bud without a callogenesis phase. Each bud whichoriginated from a single root primordium grew into a leafy shoot.Preformed root primordia of stem explants of Sesbania rostratamay constitute an excellent model for physiological researchon plant differentiation. Key words: Organogenesis, adventitious bud, preformed root primordium, conversion, Sesbania rostrata     

Lateral Root Development in Attached and Excised Roots of Zea mays L. Cultivated in the Presence or Absence of Indol-3-yl Acetic Acid

The initiation of lateral root primordia and their subsequentemergence as secondary roots have been examined in attachedand excised roots of Zea mays grown in the presence or absenceof indol-3-yl acetic acid (IAA). Exposure to IAA enhanced anlageinception in both batches of roots. In the attached roots, theIAA-induced stimulation of primordium initiation was followedby a similar increase in lateral emergence. IAA treatment, however,had no effect on the number of laterals produced, per centimetreof root, in the excised primaries. Thus, exposure to IAA didnot directly enhance lateral emergence in the attached rootsnor did it stimulate such emergence in the excised ones. Nocorrelation was found between proliferative activity in themeristem at the apex of the primary or the rate of root elongationon the one hand, and either the number of primordia initiated,or the number of laterals produced, per centimetre of primary,on the other. Zea mays, maize, root, primordium, lateral, indol-3-yl acetic acid, meristematic activity     

THE RHYTHMICAL CHANGE IN SENSITIVITY OF A LONG-DAY DUCKWEED, LEMNA GIBBA G3, TO DARK-BREAK

1. Effect of varied lengths of darkness given before continuousillumination, and that of dark-break of continuous light asa function of the time of its application, on the flower formationin a long-day duckweed, Lemna gibba G3, were studied. The results obtained suggested a rhythmic change in sensitivityto darkness, i.e., a cycle of 36 hr-period consisting of 12hr of sensitivity and the following 24 hr of insensitivity.The inhibition by darkness (12–36 hr) given before thestart of, or by dark-break (12, 24 hr) inserted in, the inductionperiod involved an extension of the induction period, but nota slow-down of the rate of flower formation. The dark-breakgiven after the induction period, however, suppressed the rateof flower production in proportion to the length of the darkness. 2. The inhibition of flowering by darkness given in the darksensitivephase was cancelled by a relatively brief light period insertedin the darkness. 3. Relation between the rhythm and the length of induction periodwas discussed. (Received August 13, 1965; )