Flowering pathway is regulated by bulb size in Lilium longiflorum (Easter lily)

Lilium longiflorum (Easter lily) vegetative propagation occurs through production of underground bulbs containing apical and axillary meristems. In addition, sexual reproduction is achieved by flowering of elongated shoots above the bulb. It is generally accepted that L. longiflorum has an obligatory requirement for vernalisation and that long day (LD) regime hastens flowering. However, the effect of bulb size and origin, with respect to axillary or apical meristems on flowering, as well as the interactions between these meristems are largely unknown. The aim of this study was to explore the effect of bulb size, vernalisation and photoperiod on L. longiflorum flowering. To this end, we applied vernalisation and photoperiod treatments to the different bulb sizes and used a system of constant ambient temperature of 25 °C, above vernalisation spectrum, to avoid cold‐dependent floral induction during plant growth. Vernalisation and LD hasten flowering in all bulbs. Large, non‐vernalised bulbs invariably remained at a vegetative stage. However, small non‐vernalised bulbs flowered under LD conditions. These results demonstrate for the first time that cold exposure is not an obligatory prerequisite for L. longiflorum flowering, and that an alternative flowering pathway can bypass vernalisation in small bulbs. We suggest that apical dominance interactions determine the distinct flowering pathways of the apical and axillary meristems. Similar floral induction is achieved in propagated bulblets from scaling. These innovative findings in the field of geophyte floral induction represent valuable applicative knowledge for lily production.     

Regeneration of bulblets from twin scales ofCrinum macowanii in vitro

Tissue culture techniques were applied to study the regeneration and growth of bulblets from bulb scale segments ofCrinum macowanii Bak. (bush- or march lily)in vitro. Shoots were induced on twin scales taken from the basal plate region of flowering-size bulbs on Murashige and Skoog (MS)-medium containing 0–20 mg l^–1 NAA and BA and a modified MS medium (MMS medium) containing 1.25 mg l^–1 ancymidol (A-Rest^TM), 0.1 mg l^–1 NAA and 0.1 mg l^–1 kinetin (ANK). Large bulblets could only be initiated on the latter. Subsequently the bulblets of 5 mm or more in diameter were trimmed and split in half, and secondary plantlets were regenerated on MMS-medium containing ANK or MS-medium without any growth regulators which in turn grew into bulblets suitable for splitting within 12–16 weeks. A total of 700–1000 bulblets could be obtained from each initial bulb within 12 months. Anatomical studies showed that the shoots were initiated from the epidermis and hypodermis on the abaxial surface of the meristematic tissue of the basal plate of the bulb scale. This technique is useful for the multiplication and preservation of a genotype, since plantlets regenerated in this manner should be genetically uniform.     

Phase change in lily bulblets regenerated in vitro

During the development of the lily ( Lilium ), three phases can be distinguished: the juvenile, the vegetative adult and the flowering phase. Juvenile bulblets sprout with one or a few leaves whereas vegetative adult bulblets sprout with a stem with elongated internodes. The transition to the vegetative adult phase was studied in lily ( Lilium  × cv. Star Gazer) bulblets regenerating on bulb scale segments in vitro. The phase change was marked by the development of a tunica-corpus structure in the apical meristem which leads to the formation of an actively growing stem primordium. This structure is absent in juvenile bulblets. Juvenile bulblets first developed competence for phase change during a culture period of at least 6 weeks at 25°C. Subsequent induction of the phase change occurred during a period of 2 weeks at lower temperature (15°C). A major factor influencing phase transition was bulblet weight. Small bulblets never formed a stem whereas large bulblets always formed a stem under inducing conditions. Large bulblets more often formed a stem than small ones but the relation between bulb growth and phase transition was not absolute. A high sucrose concentration, a large explant and a prolonged period for competence development stimulated bulb growth but also phase transition independently of growth. Lowering the concentration of MS-minerals reduced bulb growth but did not affect phase transition. Under these conditions, phase change was correlated with a low phosphorus content.     

Neoseiulus paspalivorus,a predator from coconut,as a candidate for controlling dry bulb mites infesting stored tulip bulbs

The dry bulb mite, Aceria tulipae, is the most important pest of stored tulip bulbs in The Netherlands. This tiny, eriophyoid mite hides in the narrow space between scales in the interior of the bulb. To achieve biological control of this hidden pest, candidate predators small enough to move in between the bulb scales are required. Earlier experiments have shown this potential for the phytoseiid mite, Neoseiulus cucumeris, but only after the bulbs were exposed to ethylene, a plant hormone that causes a slight increase in the distance between tulip bulb scales, just sufficient to allow this predator to reach the interior part of the bulb. Applying ethylene, however, is not an option in practice because it causes malformation of tulip flowers. In fact, to prevent this cosmetic damage, bulb growers ventilate rooms where tulip bulbs are stored, thereby removing ethylene produced by the bulbs (e.g. in response to mite or fungus infestation). Recently, studies on the role of predatory mites in controlling another eriophyoid mite on coconuts led to the discovery of an exceptionally small phytoseiid mite, Neoseiulus paspalivorus. This predator is able to move under the perianth of coconuts where coconut mites feed on meristematic tissue of the fruit. This discovery prompted us to test N. paspalivorus for its ability to control A. tulipae on tulip bulbs under storage conditions (ventilated rooms with bulbs in open boxes; 23 °C; storage period June–October). Using destructive sampling we monitored predator and prey populations in two series of replicated experiments, one at a high initial level of dry bulb mite infestation, late in the storage period, and another at a low initial dry bulb mite infestation, halfway the storage period. The first and the second series involved treatment with N. paspalivorus and a control experiment, but the second series had an additional treatment in which the predator N. cucumeris was released. Taking the two series of experiments together we found that N. paspalivorus controlled the populations of dry bulb mites both on the outer scale of the bulbs as well as in the interior part of the bulbs, whereas N. cucumeris significantly reduced the population of dry bulb mites on the outer scale, but not in the interior part of the bulb. Moreover, N. paspalivorus was found predominantly inside the bulb, whereas N. cucumeris was only found on the outer scale, thereby confirming our hypothesis that the small size of N. paspalivorus facilitates access to the interior of the bulbs. We argue that N. paspalivorus is a promising candidate for the biological control of dry bulb mites on tulip bulbs under storage conditions in the Netherlands.     

Lilium candidum bulblet and meristem development

Lilium candidum L., commonly known as the Madonna lily, is a wild Lilium species with medicinal properties and excellent potential as an ornamental crop, but one that has been scarcely investigated. The aim of this research was to study (1) tissue culture propagation of L. candidum bulblets, (2) early bulblet development, and (3) the effect of temperature and bulblet weight on bulblet and plant growth and meristem development. An investigation of the effect of explant type and temperature on in vitro bulblet propagation showed that scales were the most efficient explants for in vitro propagation and that exposing the regenerating bulblets to 15°C for 4 wk increased bulblet weight but reduced the number of bulblets produced. For bulblets planted in soil after 12 wk of exposure to 15°C or 25°C, the fastest growth was observed in the bulblets that had been exposed to 15°C and that had a larger initial size. Histological examination showed that young in vitro-grown bulblets had a rudimentary meristem comprising few cells with no layer organization. After 12 wk of growth, all bulblets showed a layered meristem, regardless of bulblet size or exposure to 15°C. However, an increased amount of leaf primordia was detected in larger bulblets. Furthermore, the histological examination revealed that in L. candidum, as opposed to other lily species, there had been no real "phase change" in the meristem and that the phase change from juvenile to vegetative adult occurred at a much later stage in L. candidum than in other species.     

Eucomis zambesiaca baker: Factors affecting in vitro bulblet induction

Eucomis species having considerable horticultural potential are used in African traditional medicine to treat various ailments. The effects of environmental and physiological parameters on the initiation and growth of bulblets using leaf explants were investigated. These included the effect of temperature (10, 15, 20, 25 and 30 °C), photoperiod (8 h light, 16 h light, continuous light and continuous dark), carbohydrates (sucrose, fructose and glucose) at different concentrations and combinations as well as various plant growth regulators; gibberellic acid (GA₃), indole-3-butyric acid (IBA), napthaleneacetic acid (NAA), N⁶-benzyladenine (BA), zeatin and others. Liquid shake and liquid static cultures versus solid cultures were investigated. Maximum number of bulblets per leaf explant was obtained at 20 °C, with an average of 3 bulbs per leaf explants and a bulblet mass of 57 mg. An 8 h light cycle produced 1.38 bulbs per leaf explant, at a mass of 42 mg. Fructose at 3% produced an average of 1.18 bulbs per leaf explant, 3.39 mm wide and weighing 56.6 mg. Of the plant growth regulators, 4.90 µM IBA was found to be the optimum treatment for bulblet induction, with an average bulb diameter of 4.36 mm and a mean bulblet mass of 79.07 mg. Liquid shake cultures exhibited poor growth while bulblet, leaf and root growth was improved in liquid static cultures. Successful micropropagation from leaf explants established that leaf explants can be used as an alternative explant source to bulbs. This protocol allows for the fast and economic mass propagation of Eucomis plants.     

Challenges associated with micropropagation of Zephyranthes and Hippesatrum sp. (Amaryllidaceae)

Summary Conventional propagation of amaryllis, Hippeastrum Herbert sp. hybrids by bulb offsets is slow, seasonal, and variable; additionally, some amaryllis hybrids do not produce many offsets. From seed, it takes approximately 2 yr to flower. Micropropagation of Zephyranthes L. sp. bulbs has challenges related to contamination of stage I cultures as well as genotype differences in culture media requirements. There are literature reports on in vitro propagation of both genera; however, the application of these reports to new cultivars leaves unanswered questions regarding surface disinfestation, explant, nutrient media, and multiplication rates. Surface disinfestation of container-grown Hippeastrum spp. hybrid cv. San Antonio Rose bulbs resulted in contamination rates of 20 to 100% in spite of various treatments, some of which killed the explant. Twin scale explants of San Antonio Rose bulbs responded on a Murashige and Skoog salt medium with 2 mg naphthalene acetic acid per 1, and transfer to soil was not a problem. In contrast, aseptically germinated seed of Zephyranthes sp. served as a suitable source of clean bulb tissue.     

Sucrose signaling function on the formation and swelling of bulblets of <Emphasis Type="Italic">Lilium sargentiae</Emphasis> E.H. Wilson

Lilium sargentiae E.H. Wilson (Liliaceae) is an ornamental and economic flowering bulb in China. Unfortunately, due to low natural bulb multiplication rates or long juvenile phases, commercial release of a new genotype may take 10 or even 20 years. In this study, bulbs were expanded in test tubes by adding sucrose, to shorten the duration of the commercial production cycle. Results indicated that when sucrose, with a concentration of 60 g l^?1, was supplied to the culture medium, the bulblets could be most effectively induced and expanded. The effect of sucrose on the formation and expansion of L. sargentiae was obvious and dominant. It was not connected to the osmotic potential of sucrose, nor entirely explained by the function of sucrose as an energy and carbon source. We used sugar analogues in the culturing of explanted materials to research the effect of sucrose-specific signaling on bulblet formation and expansion. Results showed that exogenous 3-O-methyl glucose could not induce and expand test-tube bulblets, which was similar to mannose, whereas isomaltulose could generate similar results to those obtained with sucrose. The results further indicated that the specific signalling of sucrose could be responsible for the effect on bulblets formation and swelling. We used the exclusion method to confirm above results and hypothesis, and observed that only a small part of sucrose was transformed by cell wall invertase and entered the cells through hexose transporters, playing a certain effect on bulbelt growth and development through hexose or hexose signaling systems. Overall, the effect of sucrose on bulblet induction and swelling could be explained by sucrose-specific signaling. Furthermore, this effect has a direct correlation with the sucrose-specific vector.     

The origin of bulblets formed on excised twin scales ofNerine bowdenii W. Watts

The origin of bulblets formed on excised twin scales ofNerine bowdenii was investigated anatomically. At the start of the in vitro experiments pre-existing meristems were present in the axils of the bulb scales. However, in the axils of the scale explants there were also groups of meristematic cells which developed in vitro rather quickly by mitotic divisions into thickenings and ultimately into bulb meristems. It is concluded that the formation of bulblets on excised twin scales is the result both of the outgrowth of pre-existing axillary meristems and of the regeneration of adventitious bulblets in the axils of the scales. Because more bulblets were initiated than ultimately developed, further studies to optimalize the outgrowth of primordia are needed. From an anatomical point of view there is a large potential source of in vitro bulblets.     

Effect of low temperature on dormancy breaking and growth after planting in lily bulblets regenerated in vitro

Lilies regenerating on scale segments may develop dormancy in vitro depending on the culture conditions. The dormancy is broken by storage for several weeks at a low temperature (5 °C). The effect of the low temperature on sprouting, time of leaf emergence and further bulb growth was studied. Dormant and non-dormant bulblets were regenerated in vitro on bulb scale segments cultured at 20 °C or 15 °C, respectively. The low temperature not only affected the number of sprouted bulblets but also the time of emergence. The longer the cold storage, the faster and more uniform leaf emergence occurred. Both dormant and non-dormant bulblets grew faster after a low temperature treatment of six weeks. Thus, during dormancy breaking the tissue is prepared not only for sprouting but also for subsequent bulb growth. These processes are rather independent as low temperature stimulates growth in non-dormant bulblets whereas these bulblets sprout also without treatment at low temperature. Moreover, the hormone gibberellin induces rapid sprouting but has no influence on further bulb growth. Good growth in bulblets exposed to the low temperature coincided with production of an increased leaf weight. However, the relationship is not absolute as bulblets that were cold-treated for six weeks grew larger than bulblets cold-treated for four weeks but the formation of leaf biomass was similar. During storage at low temperature starch was hydrolyzed in the bulb scales and sugars accumulated. This indicates that during this period, preparation for later bulb growth involves mobilization of carbohydrate reserves which play a role in leaf growth and development of the photosynthetic apparatus. Starch hydrolysis proceeded in the outer scales after planting. Approximately six weeks later, the switch from source to sink took place in the bulblet, which became visible as a deposition of starch in the middle scales.     

VEGETATIVE DISPERSAL IN OXALIS CERNUA

Vegetative propagation and vegetative dispersal of Oxalis cernua were studied. O. cernua is a bulbous dicotyledonous plant. The shoot of a grown plant is divided into two distinct parts: a vertical stem growing upwards and bearing the feeding roots, and a rootless horizontal thin stem. This last is pulled by means of a large contractile root and carries along with it a series of small buds, which form new bulbs at the end of the season. Several new bulbs are formed along the vertical shoot as well. Thus, the propagation bulbs of O. cernua disperse along two axes, which are at right angles to each other.     

Shoot Anatomy of Three Bulbous Species of Oxalis

The shoots of Oxalis latifolia, O. corymbosa and O. oxypteraare comprised of underground bulbs which send out stolons withapical and lateral bulbs. The external scales of the bulbs formthe base of the leaves; an adnation of the stipules to the petioleoccurs as well. In O. oxyptera the bulb shows primitive charactersand can be considered a rhizome-shaped bulb. Incipient secondarygrowth and schizo-lysigenous secretory cavities are described.An ascending evolutionary sequence of O. oxyptera, O. latifoliaand O. corymbosa is proposed based on the vegetative system. Oxalis spp., Oxalidaceae, shoot anatomy, bulb, stolons     

The productive and reproductive biology of flowering plants

The life cycles, programme of energy expenditure and allocation to reproduction, and the reproductive efforts of three wildAllium species, i.e.,A. Victorialis ssp.platyphyllum, A. monanthum, andA. Grayi, all native to Japan, were studied and compared. Furthermore, their adaptive strategies were discussed from the point of view of life history strategy. First, the reproductive systems, number of male and female gametes borne, and the number and size of propagules produced were critically investigated. In order to estimate the crude reproductive efficiency (sensu Harper and Ogden, 1970) of these species, sequential harvests were taken and the plants were divided into their component structures, dried and weighed. The quantity of dry weight allocated to sexual or vegetative reproduction was obtained by weighing the seeds, bulbils, or bulblets produced at the end of the season. A. Victorialis ssp.platyphyllum showed a rather low reproductive effort. However, the mean seed output per plant was 34.8±16.8 and the productivity appeared very constant every season. Thus, in the natural populations young plants are borne and recruited every season by means of sexual reproduction. A. monanthum was found to be characterized by annual type dry matter economy. The sexuality and reproductive systems of this species turned out to be extremely complex, and ten different reproductive types were distinguished. The exceedingly low efficiency of sexual reproduction in this species is apparently supplemented by vegetative propagation. The dry matter allocation to daughter bulbs at final harvest was very high; whereas the allocation to sexual reproduction was extremely low. InA. Grayi (a polyploid complex of 4X, 5X, and 6X), a surprisingly high amount of the total annual net assimilate is allocated to the bulbils and bulblets. On the other hand, sexual reproductive effort in this species is exceedingly low, even in obligate amphimictic plants. Thus, the recruitment of individuals in a population of this species appears to be largely dependent on vegetative reproduction. Considering the number of bulbils produced in the scape heads, their dispersibility, germinability, and rapid growth after sprouting, the bulbils evidently possess a function almost comparable to seeds. This species no doubt possesses an adapative strategy to unstable, open habitats exposed to frequent disturbances. It is concluded that the life history strategies of plants, as characterized here in this paper for three wildAllium species, have doubtlessly differentiated by adapting to the respective ecological backgrounds of their habitats.     

细叶百合无性繁殖条件的选择

以栽培的2 年生细叶百合(Lilium pumilum DC.)鳞茎为扦插材料, 将鳞茎分内、中、外三层剥取其鳞片, 观察鳞片在不同温度、光照强度、基质中的扦插生小鳞茎的效果。扦插40d 时, 鳞片基本枯萎, 此时的实验结果是:①影响扦插效果的重要因子是温度和光强, 25℃高温避光生鳞茎最佳;其次是鳞片位置, 中鳞片和外鳞片好于内鳞片;基质对扦插影响不大。②每百鳞片生小鳞茎数和小鳞茎直径呈正相关。③相同条件下, 相同部位的刀切鳞茎段所产生小鳞茎数量明显高于手掰的整片鳞片, 这一现象至今未见报导。     

The initiation of callus and regeneration from callus culture ofTulipa gesneriana

Cold treatment of seeds, obtained from crosses between cultivars ofT. gesneriana L., affects the developmental stage of embryos, which in turn influences the frequency of callus induction and the development of different callus types. Cold-treated, mature embryos and basal segments ofin vitro-derived bulblets, were suitable explants for the initiation of regenerative callus on medium with 2,4-dichlorophenoxyacetic acid. The bulblets were initiated on flower-stalk segments from cold-stored bulbs ofT. gesneriana ‘Christmas Marvel.’ Histological analyses of regenerative callus revealed the regeneration of bulb-like structures. The influences of culture medium, culture conditions, growth regulators and acetylsalicylic acid, an inhibitor of ethylene, on the initiation and establishment of regenerative callus cultures are discussed.     

A protocol for in vitro mass propagation of asiatic hybrids of lily through liquid stationary culture

Summary A simple, rapid and cost-effective in vitro scheme has been proposed for mass propagating two cultivars of Asiatic lily hybrids. An average of seven bulblets was formed after 17 d when 1×1 cm² bulb scale segments (explants) were cultured on Murashige and Skoog (MS) medium with 3% sucrose and 0.5 μM α-naphthaleneacetic acid (NAA). On MS medium containing 0.5 μM NAA and 6 or 9% sucrose, depending on the cultivar, large numbers of bulblets of increased size (3.5–5.0 cm in circumference) were formed under a 16/8 h photoperiod. A continuous system of mass propagation of bulblets was achieved through in vitro scale formation (secondary explants) on MS medium supplemented with 23 μM kinetin and 0.5 μM NAA, as well as scale proliferation on MS basal liquid stationary medium. Upon transplantation all bulblets sprouted, of which 40% flowered in the first season. Under ideal conditions, ca. 9.68×10⁵ bulblets can be produced from a single scale segment in 1 yr by following the systematic propagation steps proposed here.     

In vitro bulblet production of Brunsvigia undulata from twin-scales

Many South African medicinal plants are over-collected for use in traditional medicines. This necessitates developing methods for increasing production. Micropropagation can be used as an alternative to conventional propagation methods. Twin-scales, cut from large parent bulbs, were cultured on MS medium (Murashige and Skoog, 1962) supplemented with 25 plant growth regulator combinations. Bulblets formed on twin-scales in 24 of the treatments. All explants formed bulblets on plant growth regulator-free medium. The effect of plant growth regulators, activated charcoal, explant orientation, explant origin and photoperiod on bulblet production was investigated. Bulblet formation was greatest when twin-scales were excised from the middle of the parent bulb, placed adaxial side down on plant growth regulator-free medium and kept in a 16 h photoperiod.     

Factors affecting efficient in vitro micropropagation of Muscari muscarimi Medikus using twin bulb scale

Endemic Muscari muscarimi Medikus is the most fragrant plant among Muscari species and has a high ornamental potential. The natural populations of M. muscarimi, are severely affected by increased environmental pollution and urbanization. There is a need to develop a micropropagation method that should serve effectively for commercial propagation and conservation. Therefore, the study targeted to set up a strategy for efficient in vitro bulblet regeneration system of M. muscarimi using twin scale bulb explants on 1.0 × MS medium containing 4.44, 8.88, 17.76 μM BAP (6-Benzylaminopurine) plus 2.685, 5.37, 10.74 μM NAA (α-Naphthalene acetic acid). Maximum number of 19 daughter axillary bulblets and 16 daughter adventitious bulblets per twin bulb scale explant was regenerated on 1.0 × MS medium containing 17.76 μM BAP plus 10.74 μM NAA and 17.76 μM BAP plus 2.685 μM NAA respectively. The daughter bulblets regenerated on twin bulb scales on 8 out of 9 regeneration treatment could be easily rooted on 1.0 × MS medium containing 4.9 μM IBA (Indole-3-butyric acid). The daughter bulblets regenerated on 9th treatment (1.0 × MS medium containing 17.76 μM BAP plus 10.74 μM NAA) were transferred to 1.0 × MS medium containing 30 g/l sucrose to break negative carry over effect of this dose of BAP–NAA, where they grew 2–3 roots of variable length. Daughter bulblet diameter was increased by culturing them on 1.0 × MS medium containing 4.44 μM BAP plus 5.37 μM NAA. The results verified that both age and the source of explants had significant effect on regeneration. In another set of experiments, twin scales were obtained from in vitro regenerated daughter bulblets, although they induced bulblets, yet their bulblet regeneration percentage, mean number of bulblets per explant and their diameter were significantly reduced. In vitro regenerated bulblets were acclimatized in growth chamber under ambient conditions of temperature and humidity on peat moss, where they flowered. The study provides important information about selection of suitable micropropagation medium, strategies to improve bulblet diameter and rooting of M. muscarimi which offers a scope for commercial propagation.Abbreviations: MS medium, Murashige Skoog medium; BAP, 6-Benzylaminopurine; NAA, α-Naphthalene acetic acid; IBA, Indole-3-butyric acid     

The effect of methyl jasmonate and abscisic acid on differentiation of benzyladenine-induced bulblets inMuscari bulbs

Methyl jasmonate (JA-Me) at a concentration of 0.5% in lanolin paste totally inhibited bulblets formation induced by benzyladenine in intactMuscari bulbs. Lower concentrations of JA-Me delayed development and growth of bulblets induced by benzyladenine. It seems that methyl jasmonate acts as a powerful inhibitor of cell division induced by cytokinin in used test. In comparison with methyl jasmonate, abscisic acid did not show an inhibitory effect on bulblets formation induced by benzyladenine, even in a higher concentration.