Somatic embryogenesis and in vitro flowering inBrassica nigra

Summary This report describes a protocol for regeneration ofBrassica nigra in vitro from unorganized callus to a highly differentiated stage of flowering. Callus is initiated from seedling hypocotyl, and root explants and plantlets are obtained via somatic embryogenesis. Shoot cultures can be established from these plantlets. These shoots can either be induced to flower in vitro or rooted to produce plants which flower ex vitro. Each stage of development is marked with a specific growth regulator requirement. This has potential as a model system to understand the cellular and molecular mechanisms involved in morphogenesis, and it can be used to understand the mechanism of change of phase from vegetative to reproductive. An advantage of this system is that in vitro flowering can be obtained repeatedly in the shoots raised from the axillary buds of the flowering shoots. The protocol can also be used to procureB. nigra gametes under aseptic condition.     

Silver nitrate-induced in vitro shoot multiplication and precocious flowering in <Emphasis Type="Italic">Catharanthus roseus</Emphasis> (L.) G. Don,a rich source of terpenoid indole alkaloids

Catharanthus roseus (L.) G. Don is an economically and medicinally important plant since its leaves and flowers contain terpenoid indole alkaloids. The present study, for the first time, encompasses the influence of silver nitrate (AgNO₃), in consort with cytokinins like N ⁶-benzyladenine (BA) and 6-furfurylaminopurine (kinetin), to regenerate multiple shoots from nodal segments explants and to induce high-frequency precocious flowering of C. roseus under in vitro condition. Synergistic effect of equal concentrations of BA and kinetin was enhanced following the amalgamation of AgNO₃. As high as 98% explants responded to multiple shoot initiation and proliferation in Murashige and Skoog medium supplemented with 3 µM BA, 3 µM kinetin and 0.1 µM AgNO₃. As many as 7 shoots were developed per explant following 12 days of inoculation. Continuous culture in the same medium for 21 days induced precocious flowering from 75% shoots, wherein a maximum of ~?6 (5.67?±?0.88) flowers was observed per in vitro shoot. On the other hand, in the combinations of BA and kinetin excluding AgNO₃, a maximum of 6.67% explants responded and initiated merely 3.33 shoots per explant. Nevertheless, no induction of flower was observed in the media devoid of AgNO₃. Our results on the induction and proliferation of multiple shoots with simultaneous flowering would help the global pharmaceutical industry to produce in vitro shoots and flowers in bulk, as an alternative source of alkaloids.     

Rapid micropropagation via axillary bud proliferation of Adhatoda vasica Nees from nodal segments

A protocol for rapid multiplication of Adhatoda vasica has been developed through nodal explants from field grown mature plants. The maximum number of shoots, i.e., 7.75 +/- 0.392 differentiated from split nodal halves on MS medium supplemented with BA (10.0 mg/l) during 4 weeks of culture. Maximum number of shoots formed per explant increased to ca. 30 within 6 weeks of subculture on medium containing BA (1.0 mg/l) and Kn (1.0 mg/l). The isolated shoots rooted 90% in MS medium containing IBA (0.1 mg/l) in 2 weeks. The rooted plantlets were successfully transferred to soil in glasshouse and subsequently in field. The plantlets rooted in liquid medium did not survive, but those rooted on solid medium showed more than 75% survival. In vitro raised plants grew successfully ex vitro till flowering.     

Cost and probability of flowering at the shoot level in relation to variability in shoot size within the crown of Vaccinium hirtum (Ericaceae)

Size-related variation in the cost and probability of flowering among shoots within a crown of Vaccinium hirtum was investigated to clarify patterns and regulation of flowering at the shoot-module level, below the level of the individual. The apices of previous-year shoots differentiated into current-year shoots vegetatively (vegetative branches) or became reproductive by developing inflorescences (reproductive branches). Length growth and fate of current-year shoots were determined, and the future potential for reproduction was estimated using a matrix model of shoot dynamics. Reproductive branches had fewer current-year shoots and shorter total shoot lengths and thus had a reduced potential for reproduction compared with vegetative branches, indicating the cost of flowering at the shoot level. This cost of flowering was higher in longer shoots. The probability of the initiation of flowering in a shoot increased with increasing shoot length in shorter shoots, reached a maximum in medium-sized shoots, and decreased in longer shoots. The size-related changes in the probability of flowering at the shoot level can be largely explained by the size-dependent changes in shoot-level resource availability and cost of flowering.     

Management of below-ground biomass of <Emphasis Type="Italic">Typha angustifolia</Emphasis> by harvesting shoots above the water surface on different summer days

A dynamic model of regrowth in Typha angustifolia after cutting shoots above the water surface was formulated by characterizing the phenology and mobilization of resources from below-ground to above-ground organs after the cutting. The model parameters were determined by two cutting experiments to investigate the different strategies with flowering and non-flowering shoots after cutting in 2001 and by four cutting experiments to elucidate the regrowth characteristics after cutting on different days from June to September in 2002. A difference was evident both for flowering and non-flowering shoots and for each cutting day. From June to August, non-flowering shoots regrew immediately after cutting, but flowering shoots did not. The shoot regrowth height, number of leaves and shoot biomass were higher with the earlier cutting. The model was validated using the below-ground biomass observed in December 2002 and below-ground dynamics observed in 2003. In the low-flowering shoot zone of the stands, in which the percentage of flowering shoots was small (around 10%), the decrease in below-ground biomass became larger from June (20%) to August (60%). Cutting the high-flowering shoot zone (flowering shoots: 78%) in July 2001, just 1 week after peduncle formation, decreased the below-ground biomass by about 50%. In the low-flowering shoot zone, cutting just before senescence is better for decreasing below-ground biomass with a smaller rate of flowering shoots. The difference of below-ground biomass reduction in non-flowering shoots is mainly due to the decrease in downward translocation (DWT) of above-ground material to below-ground organs during senescence, because of the decrease in regrowth biomass. As for flowering shoots, the decrease in the photosynthate transportation from above-ground to below-ground organs and that of DWT are closely related because they cannot grow again within the season.     

Effects of shoot bending on ACC content,ethylene production,growth and flowering of bougainvillea

Several factors, such as environmental conditions, pruning, and plant growth regulators, affect the flowering of bougainvillea. However, information on the effect of shoot bending on growth and flowering of bougainvillea is scarce. In the natural environment, most of the bougainvillea flowering shoots are inclining whereas vertical shoots are not flowering shoots. Bougainvillea shoots are artificially grown vertically, horizontally and at an inclined orientation, to investigate the effect of these orientations on plant growth and the development of flower buds. The results of this indicate an effect of shoot bending on the growth rate of bougainvillea and the rate of flower bud formation. Additionally, our results suggest that vertical shoots have a higher growth rate, more prolific vegetation growth, and longer plastochrons (which are the intervals between the initiations of successive leaves). In contrast, horizontal and inclined shoots exhibited slower growth, a shorter time to reach flowering, and more flower buds. Inclined shoots had a higher endogenous ACC (1-aminocyclopropene-1-carboxylate) content and produced more ethylene than either horizontal or vertical shoots, indicating that more ACC in the inclined shoot is converted into ethylene, and the higher ethylene concentration in the inclined shoot causes it to mature earlier and flower sooner.     

On the unusual flowering of plagiotropic shoots in the seagrass Posidonia oceanica

The seagrass Posidonia oceanica (L.) Delile can produce plagiotropic (horizontally oriented) and orthotropic (vertically oriented) axes. These axes differ in various morphological and growth characteristics and ecological functions. Only orthotropic shoots are likely to support flowering and seed production. To asses whether flowering may occur on plagiotropic shoots, we examined plagiotropic axes that grew at the edge of a meadow during the flowering of 2003. We identified and analysed 10 rhizome fragments that bore at least one reproductive plagiotropic shoot. We then investigated whether reproductive plagiotropic shoots differed from orthotropic ones in morphological characteristics and investment in flowering (i.e., number of hermaphroditic flowers per inflorescence). Multivariate analysis did not show any significant difference between plagiotropic and orthotropic shoots with regard to the characteristics examined and investment in flowering. Further studies are necessary to ascertain if the observed pattern of flowering is a common or an exceptional event in P. oceanica.     

Architecture of the pruned tree: impact of contrasted pruning procedures over 2 years on shoot demography and spatial distribution of leaf area in apple (Malus domestica)

BACKGROUND AND AIMS: Demography and spatial distribution of shoots are rarely studied on pruned trees. The present 2-year study deals with the effect of pruning strategies on shoot demography and development, and consequences on the spatial distribution of leaf area in three architecturally contrasted - from type II to IV - apple cultivars: 'Scarletspur Delicious', 'Golden Delicious' and 'Granny Smith'. METHODS: All trees were initially subjected during 5 years to Central Leader training with winter heading on all long shoots. For 2 years, half of the trees were further trained with Centrifugal training, where removal of flowering shoots - called extinction pruning - was carried out along the trunk and at the bottom of branches at flowering time. During these 2 years, shoot type (vegetative, inflorescence) and length, and the three-dimensional spatial distribution of all shoots were assessed with an electromagnetic digitizer. KEY RESULTS: Shoot demography, frequency of transitions toward an inflorescence from either an inflorescence (bourse-over-bourse) or a vegetative shoot (trend toward flowering), and the number of bourse-shoots per bourse were strongly affected by cultivar, with little influence of tree manipulation. In contrast, the proportion of vegetative long shoots developing from previous year latent buds was significantly lower in Centrifugal-trained trees for the three cultivars. Canopy volume showed large variations between cultivars, but only that of 'Granny Smith' was affected by tree manipulation in the 2 years. Spatial distribution of shoots varied significantly according to cultivar and manipulation. In 'Scarletspur Delicious' and, to a lesser extent 'Golden Delicious', the distribution of vegetative and flowering shoots in the outer and the inner parts, respectively, was not affected by tree manipulation. In contrast, in 'Granny Smith', vegetative shoots were stimulated in the periphery of Central Leader trees, whereas flowering shoots were stimulated in the periphery of Centrifugal-trained trees. CONCLUSIONS: In apple, the variability of responses to contrasted pruning strategies partly depends on the genetically determined growth and flowering habit of the cultivar.     

Anthesis effects on Posidonia oceanica (L.) Delile phenology in the Bay of Calvi (Corsica,Mediterranean Sea)

In Posidonia oceanica (L.) Delile, anthesis induces a decrease in the number of juvenile leaves resulting in a significant reduction in the number of leaves on the flowering shoots. All the leaves of the flowering shoots are narrower than the leaves of nonflowering shoots. A modification of the leaf growth also appears in flowering shoots: the oldest leaves are longer and the leaves induced during or after anthesis are shorter. At 10 m depth, in the Bay of Calvi, anthesis lasts roughly 3 months and the flowering is induced 7 months before anthesis.     

Diversity of flowering and fruiting phenology of trees in a tropical deciduous forest in India

BACKGROUND AND AIMS: In the dry tropics, vegetative phenology varies widely with tree characteristics and soil conditions. The present work aims to document the phenological diversity of flowering and fruiting with reference to leafing events in Indian dry-tropical tree species. METHODS: Nine tree species, including one leaf-exchanging and eight deciduous showing varying leafless periods, were studied. Monthly counts of leaves, flowers and fruits were made on 160 tagged twigs on ten individuals of each species for initiation, completion and duration of different phenological events through two annual cycles. KEY RESULTS: Variation in flowering relative to leaf flushing (which occurred just prior to or during a hot, dry summer) revealed five flowering types: summer flowering (on foliated shoots), rainy-season flowering (on foliated shoots following significant rains), autumn flowering (on shoots with mature leaves), winter flowering (on shoots undergoing leaf fall) and dry-season flowering (on leafless shoots). Duration of the fruiting phenophase was shortest (3-4 months) in dry-season and winter-flowering species, 6-9 months in rainy-and autumn-flowering species, and maximum (11 months) in summer-flowering species. A wide range of time lag (<1 to >8 months) between the start of vegetative (first-leaf flush) and reproductive (first-visible flower) phases was recorded in deciduous species; this time lag was correlated with the extent of the leafless period. A synthesis of available phenological information on 119 Indian tropical trees showed that summer-flowering species were most abundant (56 % of total species) amongst the five types recognized. CONCLUSIONS: The wide diversity of seasonal flowering and fruiting with linkages to leaf flush time and leafless period reflect the fact that variable reproductive and survival strategies evolved in tree species under a monsoonic bioclimate. Flowering periodicity has evolved as an adaptation to an annual leafless period and the time required for the fruit to develop. The direct relationship between leafless period (inverse of growing period) and time lag between onset of vegetative and reproductive phases reflects the partitioning of resource use for supporting these phases. Predominance of summer flowering coupled with summer leaf flushing seems to be a unique adaptation in trees to survive under a strongly seasonal tropical climate.     

A Developmental Pattern of Flowering in Colored <Emphasis Type="Italic">Zantedeschia</Emphasis> spp.: Effects of Bud Position and Gibberellin

The restricted flowering of colored cultivars ofZantedeschia is a consequence of developmental constraints imposed by apical dominance of the primary bud on secondary buds in the tuber, and by the sympodial growth of individual shoots. GA₃ enhances flowering inZantedeschia by increasing the number of flowering shoots per tuber and inflorescences per shoot. The effects of gibberellin on the pattern of flowering and on the developmental fate of differentiated inflorescences along the tuber axis and individual shoot axes were studied in GA₃ and Uniconazole-treated tubers. Inflorescence primordia and fully developed (emerged) floral stems produced during tuber storage and the plant growth period were recorded. Days to flowering, percent of flowering shoots and floral stem length decreased basipetally along the shoot and tuber axes. GA₃ prolonged the flowering period and increased both the number of flowering shoots per tuber and the differentiated inflorescences per shoot. Activated buds were GA₃ responsive regardless of meristem size or age. Uniconazole did not inhibit inflorescence differentiation but inhibited floral stem elongation. The results suggest that GA₃ has a dual action in the flowering process: induction of inflorescence differentiation and promotion of floral stem elongation. The flowering pattern could be a result of a gradient in the distribution of endogenous factors involved in inflorescence differentialtion (possibly GAs) and in floral stem growth. This gradient along the tuber and shoot axes is probably controlled by apical dominance of the primary bud. Online publication: 7 April 2005     

High frequency early in vitro flowering of <Emphasis Type="Italic">Dendrobium</Emphasis> Madame Thong-In (Orchidaceae)

We have successfully developed a method to induce early in vitro flowering of the self-pollinated seedlings of a tropical orchid hybrid, Dendrobium Madame Thong-In. Transition of vegetative shoot apical meristem to inflorescence meristem was observed when young protocorms were cultured in modified KC liquid medium. In contrast, protocorms cultured on Gelrite-solidified medium only produced axillary shoots and roots. CW was required to trigger the transitional shoot apical meristem and BA enhanced inflorescence stalk initiation and flower bud formation. However, normal flower development was deformed in liquid medium but developed fully upon transferring to two-layered (liquid over Gelrite-solidified) medium. Under optimal condition, in vitro flowering was observed about 5 months after seed sowing. Segregation of flower colours was observed in these seedlings and seedpods formed upon artificial pollination of the in vitro flowers.     

Combination of thidiazuron and 2-isopentenyladenine promotes highly efficient adventitious shoot regeneration from cotyledons of mature sunflower (Helianthus annuus L.) seeds

Genetic improvement of sunflower (Helianthus annuus L.) through the use of biotechnological tools requires a reliable in vitro shoot regeneration system. Tissue culture protocols reported to date for sunflower suffer from low efficiency, poor reproducibility, genotype dependence and a tendency for flowering in vitro. The present study describes an efficient protocol system for shoot regeneration via direct adventitious shoot organogenesis from cotyledons of mature seeds of sunflower. About 169 media combinations comprising 12 different growth regulator combinations in various concentrations were assessed for induction of shoots from cotyledons derived from mature seeds and also from seedling tissues of 2?C20-day-old seedlings. Appearance of shoots from seedling tissues was sporadic and the frequency of shoot regeneration was low. Cotyledon explants from mature seeds were consistent with regard to frequency of adventitious shoot regeneration and number of shoots per explant. A high frequency (93.86?%) of adventitious shoot regeneration was obtained within 2?weeks of culture initiation on Murashige and Skoog (MS) medium supplemented with 9.84???M 2-isopentenyladenine (2-iP), 2.85???M indole-3-acetic acid (IAA) and 0.45???M thidiazuron (TDZ). Use of 2-iP in the shoot induction and elongation media prevented precocious flowering. Statistical analysis revealed significant effects of explant orientation, age of seedlings, and genotype on adventitious organogenesis. Maximum shoot regeneration was obtained when cotyledons from 0 and 1-day-old seedlings were placed with their adaxial surface in contact with the medium surface. The protocol developed was tested on 42 genotypes and found to be applicable to a wide range of genotypes. Histological studies indicated that the shoots originated predominantly through adventive organogenesis from the sub-epidermal and cortical regions.     

How does Dryobalanops aromatica supply carbohydrate resources for reproduction in a masting year?

The effect on reproduction of the dynamics of resource allocation was studied in an emergent and masting tree species, Dryobalanops aromatica (Dipterocarpaceae), in a lowland dipterocarp forest in Sarawak, Malaysia. Girdling of the reproductive shoots (5 mm diameter) caused an increase in abortion during the flowering period, but did not affect the fruit set at the middle or final stages of seed maturation. In contrast, 50% defoliation significantly affected fruit setting, but had little effect on flowering. The total leaf area of reproductive shoots was significantly correlated with final fruit set and total fruit mass. Control of the carbohydrate supply to reproductive shoots by girdling and defoliation made no difference to fruit size, but the fruit number was highly sensitive to carbohydrate availability. Total non-structural carbohydrate (TNC) decreased during the flowering period mainly in the branch (P<0.05), but fluctuated little in any organs during fruit maturation. Leaf nitrogen and photosynthetic capacity of the reproductive shoots were not significant variables for reproduction. Our results suggest that D. aromatica uses current photosynthates in the leaves of reproductive shoots as a carbon source during fruit development, but requires stored assimilates in the branch for flowering. However, since TNC was still present in all organs even after flowering, our study also suggests that storage of carbohydrate resources might not be the decisive factor in the occurrence or frequency of flowering in this species.     

Review in vitro-induced flowering in bamboos

Summary The majority of bamboos (Graminae) are arborescent and perennial. The erect stems (culms) of woody bamboos are useful for a wide variety of purposes. Most bamboos flower only once at the end of very long vegetative growth phases and die afterwards. Flowering in bamboos is thought to be under genetic control, occurring somewhat like an alarm clock, going off at a preset time. The nature of this genetic clock and any interaction between the ‘internal clock’ and the environment are not yet known. Because of this ‘peculiar’ flowering behavior, bamboo seeds are available only at very long intervals. Obtaining concurrent flowering in two or more species (or varieties) in space and time is difficult, making perennial seed propagation and genetic improvement by breeding nearly impossible. Besides, this peculiar flowering behavior of bamboos is also believed to have brought the giant pandas to the verge of extinction. One of the spectacular developments in the area of bamboo genetic improvement has been the precocious in vitro induction of flowering. By this method it has been possible to rapidly accelerate the reproductive development (within 3–6 mo. versus 30–60 yr in nature). This has opened the possibility of perennial seed propagation and hybridization. In vitro induction of flowering can be obtained by diverse methods which show some similarities and differences. Induction of flowering is possible in cultures derived from both juvenile and mature explants. The proportion of seedlings induced to flower is possibly influenced by genotypic variation, though the role of methods used cannot be ruled out. A cytokinin or a shift in the auxin-cytokinin equilibrium is believed to bring about in vitro induction of flowering. The pH of the media also has an influence. Induction of flowering and rhizogenesis is considered to be an antagonistic phenomenon in vitro. A comparison between in vitro and in vivo flowering in Bambusa arundinacea has shown that though smaller, in vitro-induced florets are comparable to normal florets. There is reduced pollen fertility and some impairment in pollen wall development. Biochemical studies on the in vitro-induced flowering in bamboos have shown (1) selective expression of esterase and peroxidase isozymes during transition of nonembryogenic calluses to embryogenic calluses, somatic embryo development, germination and subsequent flowering of somatic embryo derived shoots, and (2) minimal peroxidase activity before rhizogenesis and induction of flowering in vitro. There are reports of published and comparable methods having failed to induce flowering in vitro.     

Axillary shoot proliferation and in vitro flowering in an adult giant bamboo, Dendrocalamus giganteus Wall. Ex Munro

Summary Continuous axillary shoot proliferation and in vitro flowering were achieved using single node explants from a mature (over 70-yr-old) field clump of Dendrocalamus giganteus (giant bamboo). The shoots proliferated in a basal Murashige and Skoog medium with 6 mgl⁻¹ (26.6 μM) N⁶-benzyladenine (BA) and 2% sucrose. The rate of shoot proliferation gradually increased to over three-fold before in vitro flowering took place. In vitro flowering was not the expression of a species-specific mechanism believed to occur during gregarious flowering, as the mother clump did not flower. The rate of shoot proliferation decreased at flowering, accompanied by reversion of flowering. The development of axillary meristems into vegetative or generative shoots depended on the level of BA. The possible role of BA, changes in the rate of shoot proliferation decreased at flowering, accompanied by reversion of flowering. The development of axillary meristems into vegetative or generative shoots depended on the level of BA. The possible role of BA, changes in the rate of shoot proliferation leading to build up, and release of stress in relation to flowering and its reversion are discussed.     

In vitro floral induction from thin longitudinal sections and micro-cuttings of juvenile cork oak material

In vitro flowers were obtained from thin longitudinal sections excised at the proximity of the apical region or nodal regions of the main stem and axillary shoots of in vitro Quercus suber stock shoots as well as from field-grown seedlings. In vitro floral induction was also achieved from nodal segments of 8- to 9-month-old seedlings or from micro-cuttings of embryonic main shoot and its axillary shoots of 2-month-old seedlings. The more juvenile the material the shorter the period required to achieve flowering. Under the described experimental conditions we have thus been able to induce the expression of neoteny in a woody, long-cycle species such as cork oak.     

The inhibitory effect of gibberellic acid on flowering in Citrus

The application of gibberellic acid (GA₃) at any time from early November until bud sprouting, resulted in a significant inhibition of flowering in the sweet orange [ C. sinensis (L.) Osbeck] and the Satsuma ( C. unshiu Marc.) and Clementine ( C. reticulata Blanco) mandarins. Two response peaks were evident: the first occurred when the application was timed to the translocation of an unknown flowering signal from the leaves to the buds. The second occurred during bud sprouting, at the time the flower primordia were differentiating. From the pattern of flowering, it appears that the mechanism of inhibition was similar irrespective of the timing of GA₃ application. There was an initial reduction in bud sprouting affecting selectively those buds originating leafless inflorescences. An additional inhibition resulted in a reduction in the number of leafy inflorescences with an increase in the number of vegetative shoots, suggesting the reversion of a floral to a vegetative apex. The inhibited buds sprouted readily in vitro but invariably vegetative shoots were formed. A continuous influence of the sustaining branch is necessary to keep the flowering commitment of the buds; irreversible commitment occurs when the petal primordia are well differentiated.     

In vitro PPFD and media composition affect both in and ex vitro performance of Alstroemeria Butterfly-hybrids

The objective was to reduce in vitro production costs while retaining or improving plant quality, in particular the suitability for pot plant production. Plants were grown at photosynthetic photon flux densities (PPFD) of 0–40 μmol m^-2 s^-1 and sucrose concentrations of 3–7% during the multiplication phase and the effects of sucrose, BA, and NAA during root formation were investigated. Ex vitro growth were tested in both experiments. A small reduction in the rhizome multiplication rate was found with increasing PPFD and sucrose concentration. Increasing sucrose concentration reduced the number of aerial shoots. Aerial shoots were etiolated when cultured in darkness and their number increased with increasing PPFD at 3% sucrose, whereas PPFD did not affect the number of aerial shoots at 5 or 7% sucrose. During the multiplication phase a synergistic promoting effect of PPFD and sucrose was observed on root formation. Root formation after transfer to rooting medium was affected by sucrose and PPFD during the multiplication phase. PPFD did not influence root formation after propagation on 7% sucrose, whereas on 3 or 5 % sucrose root formation was gradually inhibited when PPFD was decreased below 17 μmol m^-2 s^-1. The formation of thick roots was promoted by propagation in light, and not influenced by sucrose concentration. Ex vitro growth was not affected by in vitro conditions, except for 7% sucrose during the multiplication phase that reduced flowering. Root formation on rooting medium was reduced by BA and promoted both by NAA and high levels of sucrose. The root inhibiting effect of BA could not completely be overcome by simultaneous application of NAA and high sucrose concentrations. Thick roots were only produced in the presence of NAA, and not affected by sucrose treatment. Ex vitro flowering was negatively influenced by the presence of BA during root formation and by high levels of sucrose if BA was absent in the rooting medium. High sucrose levels and NAA could partially compensate for the negative effect of BA on flowering. This revised version was published online in June 2006 with corrections to the Cover Date.     

EFFECTS OF AGE AND SIZE ON LIFE HISTORIES AND POPULATION GROWTH OF RHODODENDRON MAXIMUM SHOOTS

Age- and size-specific shoot life histories were studied with population censuses in June 1984 and June 1985 in an evergreen understory shrub. Rhododendron maximum. Most shoots (65%) survived without branching or flowering, and lesser numbers branched (2%), flowered (20%), or died (23%) during the year between censuses. The probabilities of surviving, branching, flowering or dying were both age- and size-dependent. Small, young shoots increased in leaf area. Flowering occurred most prominently in 3- to 6-year old shoots that had exceeded a leaf area of 200 cm², and the rate of flowering increased proportionately with size above this threshold. Branching normally occurred in the year following flowering. The age and size distributions of the population shifted significantly between years, indicating a nonequilibrium population. The survival schedule was Deevey Type I, indicating a high degree of “parental care” of young shoots. Age- and age + size-based demographic models predicted a rapid decline of the shoot population over a decade, while a size-based model predicted a much slower decline in shoot numbers. A sensitivity analysis of the models showed that overall shoot population growth was positively influenced by branching shoots and shoots that added leaf area, and negatively influenced by shoots that lost leaf area, died, or flowered. The role of shoot life histories in determining individual plant fitness and ecological dominance is discussed.