THE CONTROL OF THE ORIENTATION OF CELL DIVISIONS IN FERN GAMETOPHYTES

Time-lapse observations of filamentous fern gametophytes were used to evaluate whether the plane of cell division is referable to the plane of minimal surface area before and during the transition to two-dimensional growth. Cell dimensions of the apical cell were related to the length/width ratios associated with minimal area in the transverse plane vs. longitudinal plane, by modeling the apical cell as a hemisphere subtended by a cylinder. Our working hypothesis predicts that filamentous growth is perpetuated by an apical cell geometry that makes the transverse division plane the orientation of minimal surface area, whereas the transition to two-dimensional growth (longitudinal division of the apical cell) occurs once the longitudinal plane becomes the position of minimal surface area. The predictions of this hypothesis are fulfilled regardless of variations in light intensity and light quality, the presence of regulators of metabolism, or whether the experimental perturbation causes a corresponding selective inhibition of the transition to two-dimensional growth. Thus, the control of the plane of cell division in this system seems to depend on thermodynamic considerations of surface area. Furthermore, we favor the conclusion that the role of the genome in the transition to two-dimensional growth involves its influence on apical cell dimensions rather than the induction of specific genes for specific morphogenetic mRNAs.     

THE TRANSITION FROM FILAMENTOUS TO TWO-DIMENSIONAL GROWTH IN FERN GAMETOPHYTES. III. INTERACTION OF CELL ELONGATION AND CELL DIVISION

Periodic cell divisions were induced in gametophytes of Pteridium aquilinum by daily irradiation with white light. In white-dark cycles, the rate of cell division was promoted by increased time in white light; cell elongation was not affected. The time of transition to two-dimensional growth (days to 5% 2-D) was closely associated with the mitotic rate. For white-red cycles, the rate of elongation was controlled by the intensity of red light (wavelengths over 550 nm). This increased elongation delayed the initiation of 2-D development. In both cases the rate of transition to 2-D growth was correlated with the amount of elongation per division.     

Photocontrol of the orientation of cell division inAdiantum

The rate of transition from one- to two-dimensional growth of fernAdiantum gametophytes under white light depends on the age of gametophyte cultured under red light. When gametophytes were cultured for longer period under red light, the rate of transition decreased and the number of abnormal gametophytes increased. Although the first step of the transition was the first longitudinal cell division following the two transverse ones (Wada and Furuya, 1970), the time-lapse-video study revealed that the apical cell of protonemata became flattened in the plane perpendicular to the incident ray of white light before the first longitudinal cell division. Analytical study of growing part of the apical cell with grains of activated charcoal as markers revealed that the apical cell flattening occurred evenly throughout the equatorial circumference of the cell even in the shaded side of the protonemata as well as in the side irradiated with white light.     

GROWTH REGULATION BY ETHYLENE IN FERN GAMETOPHYTES. II. INHIBITION OF CELL DIVISION

Ethylene, a natural product of sensitive fern (Onoclea sensibilis L.) gametophytes, has been demonstrated to inhibit cell division in light-grown prothallia. When plants were grown on Knop's solution plus 1 % sucrose under 300 ft-c or more of white light, all ethylene concentrations from 1–1000 μl/liter reduced the rate of increase of cell number by about one-half. The over-all rate of increase of cell number was regulated by various environmental and chemical factors, but regardless of the rate established in control cultures, ethylene treatment of 1–1000 μl/liter produced a relative 50 % depression of cell number. Ethylene was specific for inhibition of cell division and was not a general inhibitor of growth. The ethylene inhibition did not result from a reduction of photosynthesis or energy supply. Further demonstration of ethylene as the active gaseous component resulted when cultures were grown in small enclosed containers with an ethylene absorbent, mercuric perchlorate, and consequently the cell number of gametophytes was restored to the level of unenclosed controls.     

THE TRANSITION FROM FILAMENTOUS TO TWO-DIMENSIONAL GROWTH IN FERN GAMETOPHYTES. II. KINETIC STUDIES ON PTERIDIUM AQUILINUM

Gametophytes of the fern Pteridium aquilinum were incubated 3 days in red light and then transferred to white light. The sequence of events occurring after the transfer was as follows: a swelling of the apical region within 1 hr; a reduction in cell elongation after 5 hr; a series of one-dimensional cell divisions between 10-25 hr; and the initiation of two-dimensional gametophytes after 25-50 hr. The percentage of two-dimensional gametophytes was proportional to the logarithm of the intensity of white light. The rate of elongation after 5 hr was inversely proportional to the logarithm of the intensity. The rates of cell divisions for one- and two-dimensional gametophytes were proportional to intensity up to 240 and 120 ft-c, respectively.     

INTERACTION OF LIGHT QUALITY AND NUCLEASES IN THE GROWTH OF THE GAMETOPHYTES OF ASPLENIUM NIDUS

Appropriate concentrations of ribonuclease A and B selectively inhibited initiation of two-dimensional morphology in the gametophytes of Asplenium nidus, grown under a photoperiod of 5½ hr white light. Filamentous growth was promoted in such sporelings, the individual cells of which were significantly longer than corresponding cells of the control. Higher concentrations of enzymes were required to inhibit two-dimensional growth in the gametophytes grown in blue light. Concentrations of ribonuclease A or B which inhibited two-dimensional growth in white light promoted growth in length of the protonema in red light. Growth modifications in the sporelings induced by deoxyribonuclease in different light conditions were similar to those induced by the ribonucleases. The results lend further support to the postulated role of RNA in the regulation of two-dimensional growth in fern gametophytes.     

ATTACHMENT AND FUSION OF GAMETES DURING FERTILIZATION OF PALMARIA SP. (RHODOPHYTA)1

Fertilization of cultured microscopic female gametophytes by spermatia from field-collected male gametophytes of Palmaria sp. was observed by light and transmission electron microscopy. Liberated spermatia had a prophase-arrested nucleus with a pair of polar rings. The protoplast of spermatia was covered with ca. a 3-μm-thick hyaline covering. After spermatium inoculation, the spermatial covering was attached specifically to the coat surrounding the cell wall of the trichogyne. The spermatial covering was eliminated only at the site of gamete attachment, resulting in direct attachment of the spermatial plasma membrane to the trichogyne within 5 min after spermatium inoculation. This direct attachment was followed by completion of spermatial nuclear division and cell wall formation. The polar rings disappeared before prometaphase. The cytoplasm of the binucleate spermatium invaded the trichogyne cell wall and subsequently fused with the trichogyne cytoplasm. The trichogyne could fuse with many spermatia, and many male nuclei (the derivative nuclei of spermatial nuclear division) could enter the trichogyne cytoplasm.     

THE TRANSITION FROM FILAMENTOUS TO TWO-DIMENSIONAL GROWTH IN FERN GAMETOPHYTES. I. THE REQUIREMENT FOR PROTEIN SYNTHESIS IN GAMETOPHYTES OF PTERIDIUM AQUILINUM

Two-dimensional (2-D) development of gametophytes of Pteridium aquilinum was estimated by the percentage of plants with at least one cell wall at an oblique angle, relative to the long axis. Inhibition of cell division per se was assayed by counting the cell number per filamentous (1-D) gametophyte. Specific concentrations of 8-azaguanine, 5-fluorouracil, p-fluorophenylalanine, actinomycin D, streptomycin, and cycloheximide were found to selectively inhibit 2-D development. A reduction in the percentage of 2-D gametophytes was accompanied by a reduction in the relative protein content (protein per dry weight). A comparable association was found only during the initial stages of 2-D development; after 5 days the relative protein content decreased as the percentage of 2-D gametophytes increased. Different intensities of white light resulted in a 10-fold difference in the percentage of 2-D plants with no alteration of the relative protein content. These results demonstrate that no strict relationship between 2-D development and relative protein content occurred in these gametophytes.     

岩蕨属植物配子体发育初报

本文为岩蕨属植物心岩蕨、岩蕨和耳羽岩蕨配子体个体发育和比较形态学初步研究。报道了用无机琼脂培养基由孢子培养配子体的方法。由孢子萌发到配子体成熟分四个时期:萌发期,原丝体发育期,过渡期和原叶体发育期。大多数原丝体发育到七个细胞,与顶端细胞相隔的原丝体细胞开始胞间细胞纵向分裂,进入过渡期。同时顶端细胞的横分裂受到抑制,直至原叶体顶端细胞形成开始原叶体发育期。岩蕨成熟配子体精子器盖细胞不分裂,耳羽岩蕨分裂为一个圆形细胞和一个镰刀形细胞,而心岩蕨两种情况兼而有之,配子体比较形态特征支持心岩蕨可能是以岩蕨和耳羽岩蕨为双亲的异源双二倍体的假设[5]。     

REGIONS OF CELL WALL EXPANSION IN THE PROTONEMA OF A FERN

Protonemata of Onoclea sensibilis were grown for 7 days in darkness and were then transferred into light on new media, either liquid or agar-solidified, which contained 0.15% colchicine. The growth of individual plants was observed on solid media in microchambers. Unequivocal evidence was obtained that cell wall expansion and an increase in cell diameter occurred in regions well behind the apex of the protonema. This finding is related to an hypothesis which proposes light-induced changes in microtubule orientation and cell wall structure as an explanation for certain changes in cell form in fern gametophytes.     

The distribution of plasmodesmata and its relationship to morphogenesis in fern gametophytes

Fern (Onoclea sensibilis) gametophytes when grown in the dark form a linear file of cells (one-dimensional) called a protonema. In the light two-dimensional growth occurs which results in a heart-shaped prothallus one cell thick. The objective of this paper is to relate the most common pattern of cell division observed in developing gametophytes to the formation of the plasmodesmatal network. Since the prothalli are only two dimensional, we can easily determine from thin sections the total number and the density (number per unit surface area) of plasmodesmata at each developmental stage. As the prothallus grows the number of plasmodesmata increases 50-fold in the apical or meristematic cell. This number eventually reaches a plateau even though the density continues to increase with each new cell division. What is particularly striking is that both the number and density of plasmodesmata between adjacent cells is precisely determined. Furthermore, the pattern of plasmodesmata distribution is predictable so that (1) we can identify the apical meristematic cells by their plasmodesmata number, or density, as well as by their size, shape and location, (2) we can predict, again from plasmodesmata number, the location of a future wall of the apical cell prior to its actual formation, (3) we can show that the density of plasmodesmata in the triangular apical cell of the prothallus (14 plasmodesmata microns-2) is comparable to those reported for secretory glands which are known to have high rates of plasmodesmatal transport and (4) we can show that once the plasmodesmata have been formed during division, no subsequent change in the number of plasmodesmata occurs following cell plate formation.     

THE DEVELOPMENT AND REPRODUCTIVE MORPHOLOGY OF HALOSACCION AMERICANUM I. K. LEE (RHODOPHYTA,PALMARIALES)1

Halosaccion americanum, a member of Palmariaceae, was grown in culture from spores and the life history was critically examined by the use of scanning EM and light microscopy. A mature tetrasporangium of H. americanum produces four spores that germinate to form two male and two female gametophytes. The male gametophytes grow to maturity in approximately eight months and macroscopically resemble the tetrasporophyte. Following the first division of the tetraspore, the two-celled female gametophyte consists of a vegetative cell and a carpogonium with trichogynes. Fertilization is accomplished by spermatia from male plants of the preceding generation, as male plants of the same season are immature. Spermatia are formed in a continuous layer over the surface of the mature male gametophytes and, when released, are entrained in long strands of mucous. Spermatia adhere to and fuse with trichogynes and, nuclear fusions presumably follow. The carposporophyte is absent; the new tetrasporophyte develops directly from the fertilized carpogonium. Growth of the sporophyte eventually obliterates the female gametophyte, and development into a mature tetrasporophyte proceeds over a period of approximately eight months. The development of H. americanum, with its extremely abbreviated female gametophyte stage and direct development of the tetrasporophyte from the zygote, indicates that this rhodophyte has the same life history as reported for other members of the Palmariales.     

Inhibition of two-dimensional growth and suppression of ribonucleic acid and protein synthesis in the gametophytes of the fern, Asplenium nidus, by chloramphenicol, puromycin and actinomycin D

Chloramphenicol and puromycin at appropriate concentrations inhibited the induction of two-dimensional growth in the gametophytes of the fern Asplenium nidus without drastically inhibiting germination and continued filamentous growth. Similar responses to actinomycin D were reported earlier. Radioautographic techniques were employed to study the pattern of ribonucleic acid and protein synthesis in gametophytes which were treated with chloramphenicol, puromycin and actinomycin D. Uptake of H³-uridine into ribonucleic acid was strongly inhibited by all three antibiotics. Chloramphenicol and puromycin were not as effective as actinomycin D in inhibiting H³-leucine incorporation. The results are discussed in relation to the quality of light and antibiotics on two-dimensional growth in the gametophytes.     

DIVISION OF THE GENERATIVE CELL AND LATE DEVELOPMENT IN THE MALE GAMETOPHYTE OF GINKGO BILOBA

Division of the generative cell in the male gametophyte of Ginkgo biloba to yield the sterile cell and spermatogenous cell was examined in vivo and in vitro. Evidence is presented in support of a new interpretation of development in which the sterile cell and spermatogenous cell arise from an unusual anticlinal ringlike division of the generative cell. This type of cell division is only known to occur during antheridial development in leptosporangiate ferns and stomatal development among certain ferns in the Schizaeaceae and Polypodiaceae. The strong similarities in development and cell arrangement within the male gametophytes of cycads and Ginkgo suggest that division of the generative cell in cycads may be the same as in Ginkgo. Although the ringlike (conically annular) divisions in the antheridia of leptosporangiate ferns and the male gametophytes of Ginkgo (and probably cycads) are remarkably similar and result in the production of a central spermatogenous cell, it is conjectural as to whether these patterns represent a striking convergence or evolutionary homology.     

GROWTH REGULATION BY ETHYLENE IN FERN GAMETOPHYTES. I. EFFECTS ON PROTONEMAL AND RHIZOIDAL GROWTH AND INTERACTION WITH AUXIN

Three responses resulted from the treatment with ethylene of dark-grown gametophytes of Onoclea sensibilis. Elongation of the filament was increased, elongation of the rhizoid was decreased, and cell division was inhibited. The optimal ethylene concentrations were between 0.01 and 0.1 ppm. Filament elongation was very tolerant of high ethylene concentrations, since up to 1,000 ppm did not inhibit growth below control levels. Enclosing cultures of gametophytes in chambers of limited volumes produced all the effects of treatment with ethylene, but the responses to sealing were eliminated if plants were enclosed in a chamber which contained a solution of mercuric Perchlorate. This evidence that gametophytes produced ethylene was substantiated by a direct gas chromatographic demonstration of ethylene formation. The growth-regulating effects of ethylene and auxin appeared to be independent in filament and rhizoid growth. Inhibition of elongation by supra-optimal auxin concentrations could not be attributed to an auxin-stimulated production of ethylene.     

The Relationship between the Kinetics of Ribonucleic Acid Accumulation and the Morphological Development of the Fern Gametophyte, Dryopteris borreri

Fern gametophytes were grown under blue light with and without the addition of 5-fluorouracil or 8-azaguanine, and under red light. Nucleic acids were extracted by either the detergent-chloroform or the detergent-diethylpyrocarbonate method and analyzed by polyacrylamide gel electrophoresis. No significant differences in the relative distribution of the stable RNA components accompanied the transition to biplanar growth. The RNA content per average cell decreased with growth and also varied between the cultural conditions, yet it was independent of the pattern of morphological development. The falling RNA content per average cell resulted from a progressive reduction of the RNA content of the apical cell, as determined histochemically. Since filamentous growth occurred by division of this apical cell, the rate of cell division was independent of the RNA content of the dividing cell.     

PHOTOCONTROL OF THE ORIENTATION OF CELL DIVISION IN ADIANTUM. I. EFFECTS OF THE DARK AND RED PERIODS IN THE APICAL CELL OF GAMETOPHYTES

When protonemata of Adiantum capillus-veneris L. which had been grown filamentously under continuous red light were transferred to continuous white light, the apical cell divided transversely twice, but the 3rd division was longitudinal. An intervening period of darkness lasting from 0 to 90 hr either between the 1st and the 2nd cell division or between the 2nd and the 3rd one did not affect the number of protonemata in which the 3rd cell division was longitudinal. The insertion of red light instead of darkness greatly decreased the percentage of 1st longitudinal divisions occurring at the 3rd division, and increased the number of transverse divisions. Fifty percent reduction of induction of 1st longitudinal division was caused by ca. 50 hr exposure to red light between 1st and 2nd division and by ca. 20 hr between 2nd and 3rd division, and total loss was induced by an exposure of ca. 100 hr or longer to red light in the former and by ca. 40 hr longer in the latter. Thus, by using an appropriate intervening dark period or exposure to red light, the orientation and timing of cell division could be controlled in apical cell of the fern protonemata.     

光照对蕨类植物配子体假根向重力性的影响

对８种蕨类植物配子体假根向重力性反应的研究结果表明,除卷柏Ｓｅｌａｇｉｎｅｌｌａ ｔａｍａｒｉｓｃｉｎａ Ｓｐｒｉｎｇ配子体假根无向重力性反应并且其生长方向与光照方向无关外,其它７种的配子体假根均有向重力性反应,并且假根的向重力性反应在配子体发育初期,因光照的方向不同而异,表现为负向光性。随着配子体发育至片状体阶段,光对其向重力性反应的影响逐渐减弱,而重力的影响增强。在蕨类植物配子体发育初期,光对     

Photocontrol of the orientation of cell division in Adiantum

Summary Two-dimensional prothallia of Adiantum capillus-veneris always expanded in a plane which was at a right angle to any given direction of irradiation with continuous white light. The expansion began with a longitudinal division of the apical cell, in the filamentous protonema, and the orientation of the mitotic cell plate of this first longitudinal division as well as the subsequent divisions was always parallel to the direction of the incident light. When three irradiations with white light, interrupted by periods of darkness, were given, two transverse and one subsequent longitudinal division were induced. When the last two irradiations were given from the same direction, the cell plate of the first longitudinal division in most protonemata was oriented parallel to the direction of light. However, when the direction of light during the third irradiation was at right angle to that during the second, the frequency of the longitudinal division greatly decreased but that of the third transverse division increased. Thus, the orientation of the first longitudinal division appeared to be controlled in some way not only by the irradiation which actually induced the third division but also by that inducing the preceding transverse division, while the direction of light for the first transverse division had little effect on the orientation of the third division.     

Cytokinins induce photomorphogenic development in dark-grown gametophytes of Ceratopteris richardii

The cytokinins benzylaminopurine, kinetin and isopentenyladenine induce photomorphogenesis in dark-grown gametophytes of the fern Ceratopteris richardii. At sub-nanomolar concentrations each altered the rate and pattern of cell division, elongation and differentiation, mimicking aspects of the light-mediated transition from filamentous to prothallial growth. Untreated dark-grown gametophytes grow as narrow, elongate, asexual filaments with an apical meristem. Cytokinin treatments as low as 10(-12) M reduced the length-to-width ratio through decreased cell elongation, increased periclinal cell division and induced the formation of rhizoid initials in the cells immediately below the apical meristem. Higher concentrations (10(-9)-10(-8) M) induced conversion of the meristem from apical to notch morphology. Cytokinins induced both red- and blue-light-mediated photomorphogenic events, suggesting stimulation of both phytochrome and cryptochrome signaling; however, cytokinin treatment only partially substituted for light in that it did not induce hermaphroditic sexual development or spore germination in the dark. Additionally, cytokinins did not increase chlorophyll synthesis in dark-grown gametophytes, which unlike angiosperms are able to produce mature chloroplasts in the dark. Cytokinin treatment had only slight effects on light-grown gametophytes. These results suggest evolutionary conservation between angiosperms and pteridophytes in the role of cytokinins in regulating photomorphogenesis.