The vegetative and floral development of the hybrid grape cultivar ‘Ventura’

1986 ◽  
Vol 64 (8) ◽  
pp. 1620-1631 ◽  
Author(s):  
Usher Posluszny ◽  
Jean M. Gerrath
Keyword(s):  
Fourth Order ◽  
Floral Development ◽  
Upper Arm ◽  
Grape Cultivar ◽  
Stamen Primordia ◽  
Short Style

The vegetative and floral development of the hybrid grape cultivar ‘Ventura’ was studied. A tendril forms opposite the last-formed leaf on the shoot but is slightly delayed in its initiation. Six nodes and 10 primordia complete one leaf–tendril initiation cycle. The inflorescence develops at the same site and is initially indistinguishable from the tendril. Inflorescence primordia are initiated on the upper arm, first opposite each other in a decussate arrangement and then apparently spirally. Each inflorescence primordium may subsequently initiate two lateral primordia, which become subtended by bracts. These in turn may repeat the pattern so that ultimately third- or fourth-order cysmose inflorescence branches may be produced. During floral development the calyx is initiated at first as three primordia, followed by a ring, which ultimately develops five lobes. The five corolla primordia alternate with the sepals. The five stamen primordia are initiated opposite the petals. The gynoecium initiates as five primordia, which later become a ring. Two septae are initiated opposite each other on the inner flank of the ring, forming the two-loculed ovary. Each septum forms a placenta, giving rise to two ovules. The upper portion of the gynoecial ring grows up over the ovules and forms the short style and discoid stigma.

Morphological and anatomical development in the Vitaceae. II. Floral development in Vitis riparia

1988 ◽  
Vol 66 (7) ◽  
pp. 1334-1351 ◽  
Author(s):  
Jean M. Gerrath ◽  
Usher Posluszny
Keyword(s):  
Fourth Order ◽  
Floral Development ◽  
Vitis Riparia ◽  
Stamen Primordia ◽  
Male Flowers ◽  
Female Flowers

The anatomy, morphology, and ontogeny of the flowers of Vitis riparia are presented in this paper. The inflorescence is initiated as an uncommitted primordium, which in turn initiates a bract and then bifurcates to form inner and outer "arms." Both of the arms initiate inflorescence branches, first in a decussate pattern, then in a 2/5 phyllotactic spiral. These branches may initiate pairs of lateral primordia until a series of third- or fourth-order cymose inflorescence branches is initiated. Floral development begins when the calyx is initiated as three primordia, which first merge by meristem extension and then grow out to form an indistinctly five-toothed ring. The petals and stamens arise as five common primordia, alternating with the sepals. They divide into separate petal and stamen primordia. The gynoecium arises as a ring primordium. Two septae are initiated on the inner walls of the ring and grow together to form a two-loculed ovary. Two ovules arise from each septum. In male flowers the ovules form but do not mature, and the stigma and style fail to develop. The pollen is tricolporate. In female flowers the ovules are bitegmic and anatropous, the style is short, and the stigma is discoid or two parted. The pollen lacks furrows and pores. The yellowish disc arises from the base of the gynoecium and is more prominent in male flowers. The fruit is a one- to four-seeded bluish purple berry.

Floral development of Potamogeton densus

1973 ◽  
Vol 51 (3) ◽  
pp. 647-656 ◽  
Author(s):  
U. Posluszny ◽  
R. Sattler
Keyword(s):  
Floral Development ◽  
The Other ◽  
Floral Meristem ◽  
Developmental Sequence ◽  
Initial Activity ◽  
The Third ◽  
Stamen Primordia ◽  
Procambial Strand ◽  
Inflorescence Axis ◽  
Rates Of Growth

The floral appendages of Potamogeton densus are initiated in an acropetal sequence. The first primordia to be seen externally are those of the lateral tepals, though sectioning young floral buds (longitudinally, parallel to the inflorescence axis) reveals initial activity in the region of the lower median (abaxial) tepal and stamen at a time when the floral meristem is not yet clearly demarcated. The lateral (transversal) stamens are initiated simultaneously and unlike the median stamens each arises as two separate primordia. The upper median (adaxial) tepal and stamen develop late in relation to the other floral appendages, and in some specimens are completely absent. Rates of growth of the primordia vary greatly. Though the lower median tepal and stamen are initiated first, they grow slowly up to gynoecial inception, while the upper median tepal appears late in the developmental sequence but grows rapidly, soon overtaking the other tepal primordia. The four gynoecial primordia arise almost simultaneously, although variation in their sequence of inception occurs. The two-layered tunica of the floral apices gives rise to all floral appendages through periclinal divisions in the second layer. The third layer (corpus) is involved as well in the initiation of the stamen primordia. Procambial strands develop acropetally, lagging behind primordial initiation. The lateral stamens though initiating as two primordia each form a single, central procambial strand, which differentiates after growth between the two primordia of the thecae has occurred. A great amount of deviation from the normal tetramerous flower is found, including completely trimerous flowers, trimerous gynoecia with tetramerous perianth and androecium, and organs differentiating partially as tepals and partially as stamens.

Floral development of two species of Stylidium (Stylidiaceae) and some remarks on the systematic position of the family Stylidiaceae

1992 ◽  
Vol 70 (2) ◽  
pp. 258-271 ◽  
Author(s):  
Claudia Erbar
Keyword(s):  
Key Words ◽  
Floral Development ◽  
Floral Biology ◽  
Systematic Position ◽  
Inferior Ovary ◽  
Stamen Primordia ◽  
Floral Apex ◽  
The Family ◽  
Transversal Plane

The early floral development of Stylidium adnatum and Stylidium graminifolium is characterized by an initial circular primordium whose areas in the transversal plane of the floral primordium show enhanced growth. The spiral inception of the five sepals starts before the differentiation of the initial circular primordium into two stamen primordia in transversal position (in relation to the floral diagram) and the corolla ring primordium below the stamen primordia. Then five petal primordia, which alternate with the sepals, arise on the corolla ring primordium (early sympetaly). Peculiar to the flowers of Stylidiaceae is the column that bears at its top both stigma and anthers. Probably this column should be interpreted as a receptacular tube. No distinct carpel primordia have been observed. The inferior ovary results from intercalary growth in the peripheral parts of the receptacle below the calyx, corolla, and stamen primordia. The residual floral apex gives rise to a transversal septum, by which the ovary becomes bilocular. None of the morphological, palynological, and embryological characters discussed contradicts a position of the Stylidiaceae near the Campanulales, and several of these characters support this position. Key words: Stylidiaceae, Campanulales, floral development, systematic position, floral biology.

Floral development in Melaleuca and Callistemon (Myrtaceae)

1998 ◽  
Vol 11 (6) ◽  
pp. 689 ◽  
Author(s):  
D. A. Orlovich ◽  
A. N. Drinnan ◽  
P. Y. Ladiges
Keyword(s):  
Floral Development ◽  
Flower Bud ◽  
Variable Expression ◽  
Total Absence ◽  
Stamen Primordia ◽  
Intermediate Morphology ◽  
Floral Apex

Floral development of seven species of Melaleuca and four species of Callistemon is compared. The multistaminate fascicles of Melaleuca develop from stamen primordia initiated on antepetalous pre-staminal bulges (PSBs); the resultant bundles of stamens become separated by hypanthial expansion as the flower bud enlarges. In most species of Callistemon examined the stamen primordia are initiated directly on the floral apex, and the stamens are distributed evenly around the hypanthium at anthesis. The possession of large and prominent PSBs, and thus stamen fascicles, is a feature of most species of Melaleuca and their total absence is a feature of most species of Callistemon; however, there is a continuum between these two extremes. Several taxa of both genera exhibit intermediate morphology. In C. glaucus (Bonpl.) Sweet, small but distinct PSBs develop, which influence antepetalous stamen groups that remain contiguous at anthesis. This also occurred in M. leucadendra (L.) L. This variable expression of PSBs is the result of differences in the timing of stamen initiation. Other variable features are determined by the space available for primordium initiation and the patterns of growth and expansion of the developing flower.

An updated interpretation of the androecium of the Fumariaceae

1992 ◽  
Vol 70 (9) ◽  
pp. 1765-1776 ◽  
Author(s):  
L. P. Ronse Decraene ◽  
E. F. Smets
Keyword(s):  
Key Words ◽  
Floral Development ◽  
Flower Bud ◽  
Stamen Primordia ◽  
Outer Whorl ◽  
Spatial Median ◽  
Median Position

A study of the floral development of Dicentra formosa, Corydalis lutea, and Hypecoum procumbens was carried out to better understand the nature of the androecium in Fumariaceae. Sepals emerge successively in a median position and are followed by two alternating pairs of petals. Four stamen primordia are formed in a diagonal position. They are promptly followed by two lateral, slightly externally inserted primordia. In Dicentra and Corydalis the stamens arise on two crescent-shaped protuberances. In Hypecoum, four diagonal androecial primordia fuse into two median staminal complexes. The gynoecium emerges as a girdling primordium with four growth centers. Different interpretations of the androecium are discussed. It is demonstrated that the androecium in the Fumariaceae consists basically of two whorls: an outer whorl of four alternipetalous stamens and an inner whorl of two lateral stamens superposed to the outer petals. The monothecal nature of the alternipetalous stamens and the fusion of the stamens in two triplets is probably caused by a spatial median compression of the flower bud. The androecium of Hypecoum is the result of interprimordial growth between the pairs of monothecal stamens, and the androecium of Pteridophyllum arises through the loss of the two lateral stamens superposed to the outer petals. Key words: Fumariaceae, floral development, androecium, stamen whorls.

L'androcée centripète d’Ochna atropurpurea

1978 ◽  
Vol 56 (20) ◽  
pp. 2500-2511 ◽  
Author(s):  
Fernand Pauzé ◽  
Rolf Sattler
Keyword(s):  
Floral Development ◽  
Fundamental Importance ◽  
Reliable Criterion ◽  
Early Stages ◽  
Stamen Primordia ◽  
Family Level ◽  
Definite Pattern ◽  
Phylogenetic Lineages ◽  
Floral Bud

After the inception of usually five sepals and five petals, five primary androecial primordia are initiated as broad bulges in alternation with the narrow petal primordia. On each of these primary androecial primordia, usually seven stamen primordia (i.e., secondary androecial primordia) are formed centripetally in a definite pattern. The fasciculate pattern of the androecium is noticeable only in very early stages of floral development since the stamen primordia of adjacent primary androecial primordia approach each other as closely as the stamen primordia of the same primary androecial primordium. Furthermore, the number and arrangement of the stamen primordia on the primary androecial primordia may vary even within the same floral bud. The total number of stamens per floral bud varied from 26 to 43, while the number of petals varied from 4 to 6. Some of the stamen primordia, especially among the inner ones, sometimes develop into filament-like staminodia. The findings support the view that the Dilleniidae cannot be generally characterized by a centrifugal androecium. The sequence of stamen inception is not necessarily of such fundamental importance that it is a reliable criterion for the reconstitution of major phylogenetic lineages at or above the rank of families. Shifts from a centrifugal to a centripetal androecium or vice versa may have occurred during the evolution of taxa at the ordinal (or even family) level. [Translated by the journal]

Comparative development of perianth and androecial primordia of the single flower and the homeotic double-flowered mutant in Hibiscus rosa-sinensis (Malvaceae)

1996 ◽  
Vol 74 (12) ◽  
pp. 1871-1882 ◽  
Author(s):  
Judith P. Maclntyre ◽  
Christian R. Lacroix
Keyword(s):  
Floral Development ◽  
Developmental Pathways ◽  
Partial Replacement ◽  
Double Flower ◽  
Flower Petal ◽  
Hibiscus Rosa Sinensis ◽  
Stamen Primordia ◽  
Staminal Tube ◽  
Mature Flower ◽  
Single Flower

The double-flowered variety of Hibiscus rosa-sinensis L. (Malvaceae) displays a divergent floral morphology that appears to fit the criteria for homeosis. A comprehensive definition defines homeosis as the complete or partial replacement of one part of an organism with another part. The corolla of the single flower is pentamerous. The mature flower has a staminal tube bearing 60 – 70 stamens that surrounds an exserted synstylous gynoecium with five fused stigmas. In double flowers, the outermost whorl of petals is similar in appearance to that of the single flower. The remaining floral appendages have a morphology that is intermediate between petals and stamens, to varying degrees. No two double flowers are exactly the same, even on the same plant. As with other members of the Malvaceae, floral development in both floral types is unusual: once the calyx has been initiated, a ring meristem is formed from which both petal and stamen primordia are initiated. In the single flower, petal primordia are initiated on the flank of the ring, and then stamen primordia arise in five distinct and orderly clusters. In the double flower, petal primordia are also initated on the abaxial flank, but the remainder of the ring initiates primordia that form a mixture of petals, petal – stamen intermediates, and stamens. A common ring meristem that has two different developmental pathways provides a novel opportunity to study homeosis from the perspective of comparative developmental morphology. Keywords: homeosis, Hibiscus rosa-sinensis, androecium, intermediates, ring meristem, floral development.

Morphological and anatomical development in the Vitaceae. V. Vegetative and floral development in Ampelopsis brevipedunculata

1989 ◽  
Vol 67 (8) ◽  
pp. 2371-2386 ◽  
Author(s):  
Jean M. Gerrath ◽  
Usher Posluszny
Keyword(s):  
Apical Meristem ◽  
Floral Development ◽  
Three Dimensional ◽  
Growing Season ◽  
Axillary Buds ◽  
Histological Techniques ◽  
Basal Ring ◽  
Stamen Primordia ◽  
The Common ◽  
Subsequent Activity

The vegetative and floral development of Ampelopsis brevipedunculata was studied using both three-dimensional and histological techniques. An uncommitted primordium (which usually develops into a tendril in young seedlings and a cymose inflorescence in mature plants) is initiated opposite every leaf on the flank of the shoot apical meristem. Flowers are hermaphroditic, pentamerous, and protandrous. The sepals are initiated spirally, and form a calyx unit as the result of subsequent activity of a basal ring primordium. The common petal–stamen primordia are initiated simultaneously, but differentiate into petals and stamens unidirectionally. The gynoecium is initiated as a ring primordium, which produces two septa from the inner gynoecium wall. Two bitegmic, anatropus ovules arise from the base of each septum. At maturity the gynoecium is superior and two-loculed. Pollen is tricolporate. A nectar-secreting disc arises from the base of the ovary. The fruit is a turquoise-blue berry, containing one to four seeds. Axillary buds, present at each node, develop sylleptically and normally abscise at the end of the growing season. A vertical series of as many as six serial axillary buds develop basipetally to form the overwintering buds, which are not externally visible.

Floral development and systematic position of Eucalyptus curtisii (Myrtaceae)

1991 ◽  
Vol 4 (3) ◽  
pp. 539 ◽  
Author(s):  
AN Drinnan ◽  
PY Ladiges
Keyword(s):  
Phylogenetic Tree ◽  
Floral Development ◽  
Systematic Position ◽  
Stamen Primordia ◽  
Floral Apex

The corolla of E. curtisii Blakely & White clearly consists of free, imbricate parts that closely adhere by their cuticles. Ontogenetic investigation of the corolline parts did not reveal any suggestion of morphological duality that characteristically leads to the complex 'petals' in Angophora and other eucalypts. The stamen primordia are initiated on the inner flank of the invaginated floral apex, and at anthesis are inserted on the rim of the hypanthium. There is no evidence of a stemonophore distinctive of the informal subgenera Eudesmia, Symphyomyrtus and Monocalyptus. The possession of the plesiomorphic condition for both these characters is suggestive of a 'primitive' position for E. curtisii close to the root of the eucalypt phylogenetic tree. This is supported by the possession of several other characters that are apparently plesiomorphic for Eucalyptus sens. lat.

Floral development of Butomus umbellatus

1974 ◽  
Vol 52 (1) ◽  
pp. 223-230 ◽  
Author(s):  
V. Singh ◽  
R. Sattler
Keyword(s):  
Floral Development ◽  
Stamen Primordia ◽  
Procambial Strand ◽  
Tunica Layer ◽  
Rapid Sequence ◽  
Floral Apex ◽  
Outer Tepal ◽  
Primary Pattern

The primordia of the floral appendages appear in acropetal succession and develop in the order in which they appear. The primordia of each whorl of appendages are formed in a rapid sequence. After the inception of outer tepal primordia, the floral apex becomes triangular. On each angle, one inner tepal primordium together with the primordia of a pair of outer stamens and an inner stamen is formed. The triangularity of the floral apex might be interpreted as an indication of the formation of petal–stamen (CA) primordia as reported for Alisma and Hydrocleis. If this is the case, the primary pattern of organogenesis of the Butomus flower is trimerous and tetracyclic, i.e. one whorl of outer tepals, one complex of inner tepals and stamens, and two whorls of pistils. The floral apices have a two-layered tunica surrounding a central corpus. The initiating divisions in the formation of all floral appendages occur in the second tunica layer. In the case of stamen primordia, the outer corpus is also involved. Procambial development is acropetal. One procambial strand differentiates into each floral appendage shortly after its inception. Additional procambial strands are formed in the pedicel and the perianth and gynoecium. The relationships of Butomus to the Magnoliidae are discussed.

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