REVERSION FROM FLOWERING TO THE VEGETATIVE STATE IN XANTHIUM

Lam , S. L. and A. C. Leopold . (Purdue U., Lafayette, Indiana.) Reversion from flowering to the vegetative state in Xanthium. Amer. Jour. Bot. 47(4): 256—259. Illus. 1960.–Plants of Xanthium pensylvanicum Wallr. which had been induced with short photoperiods were caused to revert to the vegetative state either by decapitation or by pinching and subsequent partial de-budding. The ability of induced plants to revert varies with the intensity of the inductive stimulus, and with the extent to which the plant is cut back. Four successive decapitation treatments caused complete reversion of almost all plants which had been given 7 inductive cycles. Reversion can be obtained after 3 inductive cycles even when all of the induced leaves remain on the plant. It is suggested that under the conditions of these experiments the synthesis of the flowering stimulus is stopped or the stimulus is immobilized in the leaves and made ineffective.     

The leaf as the site of gibberellin action in flower formation in Bryophyllum daigremontianum

Summary The long-short-day plant Bryophyllum daigremontianum can be induced to flower by transfer from long to short days (LDSD), or by gibberellin (GA) application under SD. Application of GA to mature leaves of intact or partially defoliated plants induces flowering more effectively than when applications are made to the youngest leaf pair and the shoot tip.Mature leaves on de-budded plants in SD are induced to produce floral stimulus by GA application, as demonstrated by grafting LD receptor scions onto the debudded plants, or by grafting SD leaves treated with GA onto receptor stocks in LD. This shows that GA applied to Bryophyllum in SD exerts its flower-promoting effect in the leaves.The minimal number of SD necessary for flower formation in Bryophyllum is approximately 15, both in case of photoinduction by the shift LDSD, and after GA treatment in SD. It is concluded that the LD part of photinduction establishes a high level of endogenous GAs in the leaves which is a prerequisite for production of floral stimulus under subsequent SD.Work supported by the United States Atomic Energy Commission, Contract No. AT(11-1) 1338.     

STUDIES ON THE FLORAL HISTOGENESIS AND PHYSIOLOGY OF PERILLA. II. FLORAL INDUCTION IN CULTURED APICAL BUDS OF P. FRUTESCENS

Raghavan , V., and W. P. Jacobs . (Princeton U., Princeton, N. J.) Studies on the floral histogenesis and physiology of Perilla. II. Floral induction in cultured apical buds of P. frutescens. Amer. Jour. Bot. 48(9): 751–760. Illus. 1961.—The morphological and histological changes induced in apical buds and explants of P. frutescens (L.) Britt. var. ‘Tall Late’ in short days and long days when cultured in White's medium have been followed. When photoinduced in culture, apical buds showed visible signs of changes in 30.9 days, and produced normal flowers in 81.6 days. Apical buds in LD showed similar transformations at the apices, but with continued LD treatment, they elongated to form sterile structures, superficially resembling Selaginella cones. The normal flowers formed in culture were similar to those formed on the intact plant, while the individual florets of the LD-cone differentiated only the non-sporogenous tissues in them. A less pronounced sequence of changes resulted when apical buds stripped of their older pairs of apical leaves were LD- or SD-treated. When explants with the 1st pair of unfolded leaves or with the 1st and 2nd pairs of unfolded leaves were photoinduced in vitro, the responses were relatively fast. However, explants with the 1st and 2nd pairs of unfolded leaves in LD remained entirely vegetative. When unfolded leaves were implanted in the same medium separated from the buds and both were photoinduced or given LD, the buds formed the typical 1st signs, but did not differentiate into normal flowers. This inhibition of flowering resulted in the formation of sterile cones, consisting of florets with non-sporogenous tissues only. The results have suggested the possibility of the sterile cone-like structures being an intermediate stage in the flowering of Perilla. The role of a possible inhibitor produced by mature leaves of SD plants in LD is discussed.     

Flowering induced by 5-azacytidine, a DNA demethylating reagent in a short-day plant, Perilla frutescens var. crispa

Treatment with 5-azacytidine, a DNA demethylating reagent, induced flowering in Perilla frutescens (L.) Britton var. crispa (Thunb. ex Murray) Decne. ex L. H. Bailey, an absolute short-day plant under long days. The 5-azacytidine treatment induced slight suppression of vegetative growth but had no obvious effect on any other phenotypes. The Southern hybridization analysis of the genomic DNA isolated from the leaves of 5-azacytidine-treated plants and digested with restriction enzyme, methylation-insensitive Msp I or methylation-sensitive Hpa II with P. frutescens 25S-18S rDNA intergenic spacer probe indicated that the 5-azacytidine treatment caused demethylation of the genomic DNA. The 5-azacytidine-induced flowering was delayed as compared with the short day-induced flowering. Flowers were formed even at the lower nodes which had not been directly treated with 5-azacytidine. The results suggest that DNA demethylation induced flowering by inducing the production of a transmissible flowering stimulus in P. frutescens .     

Obligatory short‐day plant,Perilla frutescens var. crispa can flower in response to low‐intensity light stress under long‐day conditions

An obligatory short‐day plant, Perilla frutescens var. crispa was induced to flower under long‐day conditions when grown under low‐intensity light (30 µmol m^?2 s^?1). Plant size was smaller under lower light intensity, indicating that the low‐intensity light acted as a stress factor. The phenomenon is categorized as stress‐induced flowering. Low‐intensity light treatment for 4 weeks induced 100% flowering. The plants responded to low‐intensity light immediately after the cotyledons expanded, and the flowering response decreased with increasing plant age. The induced plants produced fertile seeds, and the progeny developed normally. The plants that flowered under low‐intensity light had greener leaves. This greening was because of the decrease in anthocyanin content, and there was a negative correlation between the anthocyanin content and percent flowering. Treatment with L‐2‐aminooxy‐3‐phenylpropionic acid, an inhibitor of phenylalanine ammonia‐lyase (PAL), did not induce flowering under non‐inductive light conditions and inhibited flowering under inductive low‐intensity light conditions. The metabolic pathway regulated by PAL may be involved in the flowering induced by low‐intensity light.     

The relationship between gibberellin and floral stimulus inBryophyllum daigremontianum

Summary The long-short-day plantBryophyllum daigremontianum initiates flower buds both upon change from long to short day and after gibberellin application in short day only at night temperatures of 11° and 15°C, but not at 19°C.Flowering of receptor scions in long day or short day takes place just as easily when the donor stocks have been induced by the shift from long day to short day or by gibberellin treatment in short day. Leaves taken from gibberellin-induced plants can also function as donors, even better so than photoperiodically induced leaves. Receptor scions induced by gibberellin-treated donors can in turn induce other vegetative scions (indirect induction).Flower formation induced by the change from long day to short day as well as by gibberellin treatment in short day is always associated with an increased length of newly formed internodes.It is concluded that gibberellin and the floral stimulus are not identical, but that gibberellin is a factor which normally limits production of the floral stimulus inBryophyllum under short days, and that the shift from long day to short results in an increase of the gibberellin level in the plant.With 5 Figures in the TextThis work was in part supported by the National Science Foundation, grants G-16408 and G-17483.     

The transition to reproductive phase inchenopodium murale L. ecotype 197 - Early flowering long-day plant

Five days of suitable continuous light induced flowering in the majority ofChenopodium murale L. ecotype 197 plants as early as at the phase of the first pair of leaves. At the time of initiation of the 2nd to 4th pairs of leaves the capacity of plants to flower was reduced, the number of flowering plants being significantly lower under the same inductive light treatment. The capacity to flower increased again at the phase of the 5th and the 6th pairs of leaves. Inductive light treatment brought about a marked growth activation of organs present before induction, shoot apex elongation, precocious formation of new leaves and activation of axillary meristems. The course of these changes in plants of different age is demonstrated. The terminal flower developed during 5 short days following inductive light treatment. The paper shows similarities and differences between long-daymutale L. ecotype 197 and short-day C.rubrum L. ecotype 374 grown under practically uniform conditions.     

The juvenile phase inBryophyllum daigremontianum

Summary Young plants ofBryophyllum daigremontianum, which do not form flowers in response to the change from long day to short day, can easily be induced to flower by grafting onto flowering donor stocks, indicating that the growing points of young plants are fully capable of responding to the floral stimulus but their leaves are incapable of producing the latter.With 3 Figures in the TextThis work was in part supported by the National Science Foundation, grant G-17483.     

Flowering requirements of Polymnia canadensis (Asteraceae) and their influence on its life history variation

The purpose of this study is to determine the flowering requirements of Polymnia canadensis and how they correspond to the occurrence of winter annuals, biennials, and short-lived monocarpic perennials in this species. Polymnia canadensis has a vernalization requirement for flowering, and even very small plants (i.e., those with one pair of leaves) can be vernalized. Vernalized plants can flower under both long- and short days. However, to flower plants must attain a minimum postvernalization size. Plants of this primarily monocarpic species that do not die after they flower once require another period of vernalization to flower a second time (i.e., to be dicarpic). Vernalized plants exposed to high temperatures can be devernalized; these must be re-vernalized in order to flower.     

Non-reversion of Impatiens in the absence of meristem commitment

Purple-flowered plants of Impatiens balsamina maintained floral development on transfer from inductive short days (SD) to long days (LD), a treatment in which red-flowered plants of Impatiens are known to revert to leaf production. An investigation into the non-reverting nature of purple-flowered plants was carried out to establish whether these plants achieved meristem commitment or whether their non-reverting state was controlled by the leaves. When the leaves that had unfolded during the inductive SD treatment were removed at the time of transfer to LD, the purple-flowered plant did revert. This result suggests that, as in red-flowered Impatiens, meristem commitment is absent, but that purple-flowered plants maintain flowering in LD conditions because of a more permanent supply of signal from their leaves than occurs in red-flowered plants. A working hypothesis is proposed to explain how a signal from the leaves can retain a controlling role during flower development.Key words: Floral commitment, Impatiens, floral reversion, floricaula.      

Temporal changes in olfactory and oviposition responses of the diamondback moth to herbivore‐induced host plants

Temporal changes in the pre‐ and post‐alighting responses of mated female diamondback moth, Plutella xylostella L. (Lepidoptera: Plutellidae), to two species of Brassica (Brassicaceae) host plants induced by larval feeding were studied using olfactometer and oviposition assays. Females displayed strong olfactory and oviposition preferences for herbivore‐induced common cabbage (Brassica oleracea var. capitata L. cv. sugarloaf) plants over intact plants; these preferences decreased with time and disappeared by the 7th day after induction. In herbivore‐induced common cabbage plants, eggs were clustered near feeding damage on the younger leaves (leaves 5–7), whereas in intact plants, eggs were clustered on the stem and lower leaves (leaves 1–4) . However, as the time interval between larval feeding and oviposition increased, more eggs were laid on the lower leaves of induced plants. This demonstrates a change in egg distribution from the pattern associated with induced plants to that associated with intact plants. In contrast, females displayed strong olfactory and oviposition preferences for intact Chinese cabbage [Brassica rapa ssp. pekinensis (Lour.) Hanelt cv. Wombok] plants over induced plants; these preferences decreased with time and disappeared by the 5th day after induction. More eggs were laid on the upper leaves (leaves 4–6) than on the lower leaves (leaves 1–3) of intact Chinese cabbage plants at first, but the distribution changed over time until there were no significant differences in the egg count between upper and lower leaves by the 4th day post induction. For both host plant species, pre‐alighting responses of moths were reliable indicators of post‐alighting responses on the first 2 days post induction. The results suggest that temporal changes in a plant's profile (chemical or otherwise) following herbivory may influence attractiveness to an insect herbivore and be accompanied by changes in olfactory and oviposition preferences.     

Gibberellin-like substances in Bryophyllum daigremontianum and the distribution and persistence of applied gibberellin A3

Summary Acidic extracts of the long-short-day plant Bryophyllum daigremontianum contain two gibberellin (GA)-like substances called fractions I and II. In plants under permanent short-day (SD) conditions the levels of both I and II are very low. In continuous long days (LD) the total GA content is approximately 20 times higher than in SD, mainly due to an increased level of II. Extracts of plants induced to flower by the shift LDSD show a further increase in the level of II. Application of GA₃ to plants in SD causes normal flower formation, but the level of fraction II remains as low as in vegetative plants in permanent SD.Approximately 10% of the GA₃ applied could still be recovered from leaves and inflorescences after 45 days, indicating that GA₃ is very stable in Bryophyllum, Most of the GA₃ recovered was still associated with the treated leaves, but small amounts could be detected in other leaves and in inflorescences. Results of grafting experiments indicate that these low levels of GA₃ are adequate to induce production of the floral stimulus.     

Changes in the Protein Composition of the Shoot Apical Bud of Sinapis alba in Transition to Flowering

Vegetative plants of Sinapis alba L. grown in short days were induced to flower by expsoure to one or continuous long days. In both inductive conditions, the first flowers were initiated about 60 h after the start of the treatment. Soluble protein extracts were prepared from apical buds and just-expanded leaves of both vegetative and induced plants. Rabbit antisera were prepared using extracts from vegetative and reproductive buds. Immunodiffusion tests were performed. Analysis of the precipitin bands indicated that: (1) one antigenic protein was present in the vegetative buds and disappeared from the buds of induced plants between 96 and 240 h after the start of the inductive treatment; (2) the concentration of a another antigenic protein increased in buds of induced plants 30 h after the start of the inductive treatment; (3) the concentration of a third antigenic proteín increased in buds of induced plants at 96 h.     

Contributo alla flora del valdarno superiore

Summary

Considering variously aged individui of the short-day plants Chenopodium amaranticolor Coste et Rein, and Perilla ocymoides Lour. var. nanckinensis Voss., researches were carried out concerning differences in photoperiodic behaviour due to ontogenetical progress and other conditions.

Experiments showed that plants behave photoperiodically in a quantitative different manner in relation to age degree. In connection with ontogenetic progress there is a lowering in the minimal anto-inductive number of fotocicli (short day); if a series of fotocicli is given, the minimal duration of the photophase, as well as the need of light intensity, are also lowered. Chenopodium plants, cultivated during 14 weeks in long days, shows — as an extreme manifestation — the ability to form inflorescence primordia even only after one photoinductive ciclus treatment. (i. e. one 16-hours nictophase). Perilla plants cultivated during 16 weeks in long days (more aged plants were not taken into consideration) are able to form inflorescence primordia after 3 photo-inductive cicli (12-hours nictophases). Also these plants, nevertheless, form infl. primordia by means of the action of one nictophase solely, provided this nictophase is cospicuosly prolonged beyond the critical duration; the nictophase shows, in this case, a florigenic action (of particular character: see below) that goes further quantitatively in connection with the exceeding prolongation of conditions of darkness beyond the critical point. The samething may be said for Chenopodium 10-weeks old plants (that do not form infl. primordia with one nictophase of 16 hours). All these tests are able to form infl. primordia in continuous darkness and, always in dark conditions, form possibly flower and liable seeds. Young individui do not behave as aged ones. The age is not the only requisite that grants to the plants this behaviour; such characteristics depends also on the general conditions of nutrition, etc.; therefore, according to the conditions of culture, plants will have the same prerogatives at differents ages.

As to the problem of mechanism under which the infl. primordia formation and flowering is afforded in continuous darkness, and in general in connection with the causes determining the variations in photoperiodical behaviour with aging, many possibilities are discussed. Special importance has been granted to the fact that the individuus, with aging, becomes by and by anto-autonomous (at various degrees) owing to the slow accumulation of eu-florigenic materials formed in long-day conditions.

The anto-autonomous plants are able to form infl. primordia, in darkness, even leaveless (plants deprived of leaves before the treatment): storage occurs expecially in the stem or stock; the storage eu-florigenic substances may be considered simply trophic substances, but of a certain composition and quantity.

The anto-autonomous plant, even at a high degree, do not flower in long-day condition owing to a mechanism of pure photoperiodic anto-inhybition. In continuous darkness it flowers essentially owing to the euflorigenes reserves (a positive factor) and — at the same time — owing to the inability of leaves and stem parenchims to actualise any antiflorigenic process (negative factor).

Many problems are object of discussion and will be bound to further experimental work. Thus the behaviour of leaves in continuous darkness or in a dark-period prolonged beyond the critical point. The leaves of aged plants do not seem to remain, in this case, merely actionless in as much as it concerns the developmental processes.     

Phloem Exudate of Perilla crispa and its Effects on Flowering of P. crispa Shoot Explants

The aim was to develop an assay for the flowering stimulus ofa photoperiodically-sensitive plant. Phloem exudate solutionswere obtained from photoperiodically induced and non-inducedleaves of Perilla crispa (Thunb.) Tanaka, following treatmentof excised leaves with solutions of EDTA or phytic acid. Theamounts of exudate obtained were estimated polarimetrically,and the conditions for obtaining maximum exudate yields weredetermined. Shoot explants from non-induced P. crispa plantswere grown on a nutrient medium. Under short days the explantsreached anthesis after c. 35 d. In continuous light a smallproportion of the explants showed signs of flowering after 100d. The effects of test substances and phloem exudate on theflowering of explants grown in continuous light was investigated.(?)-ABA (4.0 µM), sucrose (14.6 mM) and phloem exudatefrom both induced and non-induced leaves caused some promotionof flowering. In three experiments, phloem exudate from inducedleaves enhanced flowering to a greater extent than exudate fromnon-induced leaves; in other experiments the effects of thetwo types of exudate were similar. There was no evidence thatABA or sucrose in the phloem exudate caused flowering. Concentrationsof phloem exudate above 2.0 g I^–1 were phytotoxic to theexplants. Key words: Chelating agents, Flowering, Perilla crispa, Phloem exudate, Phytic acid, Shoot culture     

Florivory by a floriphilic katydid,Phaneroptera brevis,induces changes in a leaf trait in Lantana camara

1. Plants can induce a response when they are attacked by herbivores. Although the induction of responses by herbivory in both flowers and leaves is relatively well studied, whether florivory (feeding of flowers) can also induce responses in flowers and leaves is less well explored and there are still unanswered questions. These include whether plants exhibit different levels of induced responses depending on the length of exposure to the florivores. 2. To address this knowledge gap, this study used a tropical floriphilic katydid, Phaneroptera brevis, and its non‐native food plant, Lantana camara. Nursery experiments were performed in which dry matter content and anthocyanin concentration of the flower (corolla and stamens), leaf dry matter content, and leaf blade punch resistance were measured at three time phases before and after exposing the plant to the katydid individuals for 0–7 days. 3. It was demonstrated that increasing the length (days) of exposure to the katydid individual leads to higher levels of induced plant response (leaf blade punch resistance), but only in the leaves. It was also shown that higher levels of induced plant response owing to the increase in the length of exposure to the katydid individual was not observed beyond the first set of leaves developed after the exposure. 4. These results address the knowledge gap and show that plants can exhibit different levels of induced responses depending on the length of exposure to florivores. This study thus highlights the far‐reaching importance of florivory on plants.     

Oviposition preference of western flower thrips for cucumber leaves from different positions along the plant stem

While the distribution of herbivorous insects over leaves along the stem often shows a peak at some distance from the apex this does not necessarily reflect an innate preference as alternative explanations can be provided such as impact of predators and inter- or intraspecific competitors. It is of interest to determine which factors shape the distribution of insects over the leaves of a plant. Do leaves from different positions differ in suitability for insects and is that reflected in the insect's preference, or are other factors involved? In this paper we assess how the herbivorous insect western flower thrips, Frankliniella occidentalis (Pergande) (Thysanoptera: Thripidae), chooses among leaves from different positions relative to the apex of cucumber, Cucumis sativus (L.) plants. On leaf discs of a susceptible and three partially resistant cucumber accessions, thrips reproduction was highest on apical leaves and lowest on basal leaves. In dual-choice essays thrips females preferred younger leaves over older leaves for oviposition in all cucumber accessions tested, as was predicted from the no-choice assay. This indicates that differences in leaf suitability are an important factor in determining thrips distribution on cucumber plants.     

Induction of systemic resistance to bacterial blight caused by Xanthomonas campestris pv. malvacearum in cotton by leaf extract from a medicinal plant zimmu (Allium sativum L. × Allium cepa L.)

Abstract

Aqueous extract (10%) from leaves of zimmu (Allium sativum L. × Allium cepa L.) when applied as foliar spray to first and second leaves of cotton plants induced systemic resistance in third and fourth leaves to a challenge infection with Xanthomonas campestris pv. malvacearum and reduced the number of lesions by up to 73% compared with water-treated control plants. The treated leaves exhibited significantly high activity of enzymes phenylalanine ammonia-lyase, peroxidase and polyphenol oxidase along with rapid accumulation of phenolics. The activities of chitinase and β-1,3-glucanase were greatly elevated in treated plants as compared to water-treated controls. An 11-fold increase in chitinase activity was evident 4 d after treatment. Western blot analysis revealed that a chitinase with an apparent molecular weight of 58 kDa that cross-reacted with a barley chitinase antiserum was induced in cotton leaves 3 d after treatment and the maximum induction of this chitinase was detected 4 d after treatment. The present study provides evidence for the induction of biochemical defence mechanisms in cotton leaves after treatment with leaf extract from zimmu.     

Thigmomorphogenesis: The response of plant growth and development to mechanical stimulation

Summary When young plants of Hordeum vulgare. Bryonia dioica. Cucumis sativus. Phaseolus vulgaris. Mimosa pudica. and Ricinus communis. were given a gentle mechanical stimulus by rubbing the internodes for about 10 s once or twice daily, elongation was significantly retarded. Plants of Cucurbita pepo Pisum sativum and Triticum aestivum did not exhibit any such response. The initial response to rubbing was very rapid, elongation stopping less than 3 min after application of the stimulus. When the stimulus was discontinued after 7 days, elongation accelerated, reaching a normal or supernormal rate within 3 or 4 days. Mechanical stimulation also affected aspects of growth and development other than stem elongation. In Mimosa pudica, flower bud production was retarded, as was the growth of the tendrils, leaves, and petioles in Bryonia dioica. It is suggested that this response be called thigmomorphogenesis, and that it represents an adaptation designed to protect plants from the stresses produced by high winds and moving animals. Some evidence indicates that thigmomorphogenesis may be mediated by ethylene.