Novel variation in the floral development of two species of Parthenocissus

2003 ◽  
Vol 81 (7) ◽  
pp. 738-748 ◽  
Author(s):  
Trevor Wilson ◽  
Usher Posluszny

This study compares the development of the inflorescences and flowers of Parthenocissus quinquefolia (Virginia creeper) and Parthenocissus tricuspidata (Boston ivy). The development of the reproductive shoots is described from inception to maturity using epi-illumination and scanning electron microscopy. In both species, the shoot apex initiates inflorescence primordia low on the apical flank. An inflorescence primordium produces several bract-opposed branches, which in early development resembles the main shoot. As inflorescence development continues, branch primordia initiate as increasingly larger portions than the inflorescence apical meristem. By late development, branch primordia initiate as larger portions than the apex, which is a process that has been observed in other vitaceous inflorescences. With respect to initiation and early development, the Parthenocissus inflorescence is very similar to the tendril, which has been previously studied; these two organs have never been described to be so similar, and their likeness to the shoot, in early development, provides an idea as to how they may have arisen. An inflorescence branch terminates as a dichasium, which is formed by two nearly simultaneous branching events. Parthenocissus tricuspidata flowers develop a more robust gynoecial disc and stigma than in the P. quinquefolia flower; but the calyx is ring-like in the former and cup-like in the latter. Contrary to the previous assumption that there are no differences in reproductive biology within genera of the Vitaceae, this study has clearly demonstrated variation between two species of Parthenocissus.Key words: floral, development, monopodial, Parthenocissus, inflorescence, Vitaceae.


2006 ◽  
Vol 84 (5) ◽  
pp. 702-716 ◽  
Author(s):  
Trevor C. Wilson ◽  
Jean M. Gerrath ◽  
Usher Posluszny

Vegetative and floral development of Cyphostemma simulans (C.A. Small) Wild & Drummond, Cyphostemma juttae (Dinter & Gilg) Descoings, and Cyphostemma mappia (Lam) Galet were compared using epi-illumination light microscopy and paraffin sectioning. Cyphostemma simulans is a liana with leaf-opposed tendrils and inflorescences, which both arise from the shoot apical meristem, whereas the other two species are shrubs that lack tendrils and their main shoot terminates in an inflorescence. A shoot apical meristem of C. simulans can be overtopped by an inflorescence, making the architecture appear to develop like a sympodium, which is the architecture shared by the other two species. On the other hand, a terminal inflorescence of C. juttae or C. mappia can be placed in a leaf-opposed position by a precocious axillary branch, making the architecture appear to develop like a monopodium, which is the typical architecture of the Vitaceae. The floral development of all three species is similar in early ontogeny, except for a difference in calyx development between C. mappia and the other two species. Later developmental differences of the septum and gynoecium, in addition to flower colour and phenology, are distinct characteristics that distinguish flowers of each species. Therefore, this study is the first to demonstrate differences in the floral characteristics of Cyphostemma. In addition, it shows how each architecture type (monopodium or sympodium) can resemble the other and so provides stronger evidence about how the unique architecture of the Vitaceae has originated.



2006 ◽  
Vol 33 (1) ◽  
pp. 31 ◽  
Author(s):  
Paul K. Boss ◽  
Lekha Sreekantan ◽  
Mark R. Thomas

Grapevines (Vitis vinifera L.) have unusual plant architecture in that the shoot apical meristem produces both vegetative structures and primordia that are capable of forming inflorescences at regular intervals. These primordia are termed ‘uncommitted’ and differentiate into inflorescences or tendrils depending on the environment in which they are produced. To investigate the molecular relationship between tendrils and inflorescences and vine architecture, we cloned a TFL1 homologue from grapevine (VvTFL1). VvTFL1 is expressed in shoot apices early in latent bud development and in buds soon after bud burst. The grapevine homologue of LEAFY, VFL, is expressed at the same stages as VvTFL1 as well as in the later stages of inflorescence development. Neither VvTFL1 nor VFL were detected in tendrils. VvTFL1 was overexpressed in tobacco and Arabidopsis to confirm that it was functionally similar to TFL1 and not the close homologue FT. Flowering was delayed significantly in tobacco and Arabidopsis transformants overexpressing VvTFL1. However, an unexpected phenotype was observed in some of the transgenic Arabidopsis lines where the floral meristem became indeterminate and a new inflorescence would emerge from within the developing silique. Our findings suggest that VvTFL1 is a repressor of floral development. The nucleotide sequence reported in this paper has been submitted to GenBank under the accession number AF378127 (VvTFL1).



2003 ◽  
Vol 81 (6) ◽  
pp. 587-597 ◽  
Author(s):  
Trevor Wilson ◽  
Usher Posluszny

This study compares the developmental morphology of Parthenocissus quinquefolia Planch. (L.) (Virginia creeper) with that of Parthenocissus tricuspidata (Sieb. & Zucc.) Planch. (Boston ivy) to better understand how the tendril is related to the main shoot architecture of the Vitaceae. Tendril development is looked at from inception to maturity using scanning electron microscopy and epi-illumination microscopy. A tendril primordium is initiated low on the periphery of a shoot apical meristem; this pattern of development is reminiscent of typical monopodial shoot development. A tendril "shoot" in turn produces several bract-opposed branches and resembles the main shoot in its early development. However, a tendril develops through lateral growth, and because it lacks lateral buds, its architecture appears more sympodial than the main shoot. As more tendril branches are produced, the tendril "shoot" pattern of development gradually changes to a pattern of development reported in other vitaceous tendrils. This shift in development suggests how other vitaceous tendrils may be related to the shoot. Because tendril development in Parthenocissus can be demonstrated to be sympodial, it lends evidence to the idea that the unique monopodial-like system in members of the Vitaceae may be derived. The main shoot and tendril development are more similar than has previously been shown.Key words: Vitaceae, Parthenocissus, monopodial, sympodial, tendril, development.



1963 ◽  
Vol 41 (12) ◽  
pp. 1663-1674 ◽  
Author(s):  
D. J. C. Friend ◽  
J. E. Fisher ◽  
V. A. Helson

Under continuous illumination, floral initiation was earlier with each increase in light intensity from 200 to 2500 ft-c, and with each increase in temperature between 10 and 30 °C. This effect of light intensity is attributed to promotion of floral initiation by energy in the far-red (730 mμ).The rate of formation of leaf primordia was accelerated by increases in light intensity to a greater extent than floral initiation, so that the final leaf number on the main shoot was greatest for the plants grown at high light intensities. Between 10 and 25 °C an increase in temperature had similar effects on the rate of formation of leaf primordia and floral initiation, so that the final leaf number was not altered. The final leaf number was lower at 30 °C than at 25 °C because leaf primordium formation was retarded.After floral initiation, the growth of the apical meristem was most rapid at 30 °C and 2500 ft-c, resulting in the earliest heading and anthesis (33 and 38 days). Low temperatures strongly retarded the later stages of ear development and emergence.



Development ◽  
2000 ◽  
Vol 127 (6) ◽  
pp. 1267-1276 ◽  
Author(s):  
P.D. Jenik ◽  
V.F. Irish

The shoot apical meristem of Arabidopsis thaliana consists of three cell layers that proliferate to give rise to the aerial organs of the plant. By labeling cells in each layer using an Ac-based transposable element system, we mapped their contributions to the floral organs, as well as determined the degree of plasticity in this developmental process. We found that each cell layer proliferates to give rise to predictable derivatives: the L1 contributes to the epidermis, the stigma, part of the transmitting tract and the integument of the ovules, while the L2 and L3 contribute, to different degrees, to the mesophyll and other internal tissues. In order to test the roles of the floral homeotic genes in regulating these patterns of cell proliferation, we carried out similar clonal analyses in apetala3-3 and agamous-1 mutant plants. Our results suggest that cell division patterns are regulated differently at different stages of floral development. In early floral stages, the pattern of cell divisions is dependent on position in the floral meristem, and not on future organ identity. Later, during organogenesis, the layer contributions to the organs are controlled by the homeotic genes. We also show that AGAMOUS is required to maintain the layered structure of the meristem prior to organ initiation, as well as having a non-autonomous role in the regulation of the layer contributions to the petals.



Development ◽  
1992 ◽  
Vol 116 (2) ◽  
pp. 397-403 ◽  
Author(s):  
H. M. Ottoline Leyser ◽  
I. J. Furner

The shoot apical meristem of dicotyledonous plants is highly regulated both structurally and functionally, but little is known about the mechanisms involved in this regulation. Here we describe the genetic and phenotypic characterisation of recessive mutations at three loci of Arabidopsis thaliana in which meristem structure and function are disrupted. The loci are Clavata1 (Clv1), Fasciata1 (Fas1) and Fasciata2 (Fas2). Plants mutant at these loci are fasciated having broad, flat stems and disrupted phyllotaxy. In all cases, the fasciations are associated with shoot apical meristem enlargement and altered floral development. While all the mutants share some phenotypic features they can be divided into two classes. The pleiotropic fas1 and fas2 mutants are unable to initiate wild- type organs, show major alterations in meristem structure and have reduced root growth. In contrast, clv1 mutant plants show near wild-type organ phenotypes, more subtle changes in shoot apical meristem structure and wild-type root growth.



1982 ◽  
Vol 60 (8) ◽  
pp. 1437-1446 ◽  
Author(s):  
Darleen A. De Mason ◽  
Kenneth W. Stolte ◽  
Brent Tisserat

Inflorescence primordia in the date palm (Phoenix dactylifera L.) differentiate within axillary buds in November in the Coachella Valley, California. The rachillae are initiated as small mounds without subtending bracts on the flattened apex of the rachis and are enclosed by the prophyll. A single bract subtends each flower primordium. Flower primordia are initiated in an acropetal sequence along the rachillae. Although mature flowers are functionally unisexual, early development is similar in staminate and pistillate flowers. Six perianth parts are initiated within two alternating whorls: the sepals and the petals. Six stamens are initiated in two alternating whorls of three stamens each, the first opposite the sepals and the second opposite the petals. Lastly, three separate carpels are initiated. Pistillate and staminate flowers are identical and apparently bisexual at this stage. The two flower types diverge developmentally when the stamens become bilobed and elongate in the staminate but not the pistillate flowers. The pistillodes in the staminate flowers form rudimentary stigmatic surfaces at the tip of the carpels and meristematic lumps corresponding to the position of the ovule in normal carpels. The staminodes mature in the pistillate flowers as small triangular projections. Meiosis occurred in staminate and pistillate flowers (in March 1979) when the staminate flowers were about 5 mm long and the pistillate flowers were about 3 mm long.



HortScience ◽  
1990 ◽  
Vol 25 (9) ◽  
pp. 1086f-1086
Author(s):  
M. G. Karlsson ◽  
J. W. Werner ◽  
H.C.H. McIntyre

The effect of temperature during the initial long day period on morphology and plant dry weight was determined for Begonia × hiemalis `Hilda'. Multistem cuttings were planted in 10 cm pots and grown at 13°, 16°, 19°, 22°, 25° or 28°C. The day length was 16 hours at an irradiance level of 280 ± 20 μmol·m-2s-1. After 21 days, the plants were moved to a greenhouse maintained at 20° ± 2°C and short days of 10 hours at 125 ± 20 μmol·m-2s-1. The plants were grown under short days for 14 days and then moved to a day length of 16 hours. At data collection 21 days later (56 days from planting), plant height averaged 185 mm for plants initially grown at 13°, 16°, 19° or 22°C while pants originally grown at 25° and 28°C were 40 and 78 mm shorter than plants started at lower temperatures. The mean number of shoots was 4 on plants exposed to 16°, 19°, 22° or 25°C during early development and decrease to 3 shoots for plants grown initially at 13° or 28°C. The average flower number on the main shoot was similar for plants first exposed to low and intermediate temperatures but decreased rapidly to 0 for plants with early exposure to 28°C. Plants in treatments with early temperatures of 19° or 22°C had the largest above ground dry weight at an average 460 mg.



HortScience ◽  
2006 ◽  
Vol 41 (4) ◽  
pp. 1052B-1052 ◽  
Author(s):  
Tomoya Esumi ◽  
Ryutaro Tao ◽  
Keizo Yonemori

Japanese pear (Pyrus pyrifolia) and quince (Cydonia oblonga), both classified in the subfamily Maloideae, show differences in inflorescence architectures despite of the fact that they are genetically closely related. We previously isolated flowering related genes, LEAFY (LFY) and TERMINAL FLOWER 1 (TFL1) homologues, from these species and showed that they had two types of homologues for each gene. In this study, we examined the expression pattern of LFY and TFL1 homologues in these species by in situ hybridization and RT-PCR. The floral bud was dissected to small pieces under stereomicroscope; apical meristem, scales/bracts, pith, floral meristem, and inflorescence; and then used for RT-PCR. The LFY homologues were expressed in apical meristem and scales/bracts before the floral differentiation in both Japanese pear and quince. After floral differentiation, the expression was observed in floral meristem, scales/bracts and pith in both the species. The TFL1 homologues were strongly expressed in the apical meristem, but their expression was drastically decreased just before floral differentiation. It is considered that the decrease of expression of TFL1 homologues is a sign of floral initiation. The expression of TFL1 homologues was transiently increased at the beginning of floral differentiation in both species. Moreover, one of TFL1 homologues in Japanese pear was continuously expressed in the inflorescence part in the floral primordia, whereas expression of TFL1 homologues in quince almost completely disappeared after a solitary floral meristem was initiated. It was suggested that TFL1 homologues may also be involved in the inflorescence development of Japanese pear.



2017 ◽  
Vol 18 (4) ◽  
pp. 1624-1631
Author(s):  
TRI HANDAYANI

Handayani T. 2017. Flower morphology, floral development and insect visitors to flowers of Nepenthes mirabilis. Biodiversitas 18: 1624-1631. Nepenthes mirabilis Druce is a commercial ornamental pitcher plant belonging to the Nepenthaceae. This species is often used as a parent plant in artificial crossbreeding. The plant is also used in traditional medicine, rope-making, handicraft, and bouquets. Flower development and pollen maturity are important factors in pitcher plant crossbreeding. However, information about its flowering is still lacking. This study aimed to record the flower morphology, flower development, and faunal visitors to male inflorescences of N. mirabilis planted in Bogor Botanic Gardens, West Java, Indonesia. Twelve racemes of flowers were taken as a sample for observing the process of inflorescence development, while ten flowers on each raceme were observed for investigating the flowering pattern of individual flowers. The morphology of flowers, the process of inflorescence development, the flowering pattern for individual flowers, the number of open flowers, the longevity of anthesis, and the appearance of insect (and/or other faunal) visitors to flowers were observed and recorded, using naked eyes, a hand lens, and a camera. Six phases of inflorescence development were identified: inflorescence bud phase, raceme phase, the opening of the raceme-protecting sheath phase, inflorescence-stalk and flowerstalk growth phase, open flower phase and pollen maturity phase. Four phases of flower development were observed: growth of flower bud, the opening of tepals, pollen maturation, and flower senescence. The pattern of anthesis within an inflorescence was acropetal. The number of flowers per raceme was 56 to 163. The peak duration of anthesis of a flower was 11 days (30.7% of flowers). The length of the raceme-stalks was 17-31 cm. The length of the racemes was 23-38 cm. The most common visitors to the flowers were stingless bees, Trigona apicalis.



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