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.

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.

Biology of Australian seagrasses: Floral development and morphology in Amphibolis (Cymodoceaceae)

1982 ◽  
Vol 30 (3) ◽  
pp. 251 ◽  
Author(s):  
CA McConchie ◽  
SC Ducker ◽  
RB Knox
Keyword(s):  
Floral Development ◽  
Female Flower ◽  
Floral Meristem ◽  
Ovary Wall ◽  
Male And Female ◽  
Mature Flower ◽  
Male Flowers ◽  
Lateral Branches ◽  
Floral Vasculature ◽  
Female Flowers

Floral development of male and female flowers in Amphibolis antarctica and A. griffithii was followed from the initiation of the floral meristem to the mature flower. In A. antarctica the flowers form on lateral branches, while in A. griffithii they may also develop terminally on an upright branch from the rhizome. A. griffithii and. to a lesser extent, A. antarctica, show sympodial branching from the floral axis. The female flower develops from a pair of primordia; in A. griffithii these primordia each develop three stigmas, which in A. antarctica subsequently may form secondary branches. The. ovary wall bears the initials of the future grappling apparatus, comprising four comb initials in A. grijjjthii and a further inner set of horns in A. antarctica. The female flowers of Amphibolis are unique amongst the members of the Cymodoceaceae in being subtended by a bract or perianth, similar to the male flowers. Differences between the floral vasculature and intravaginal squamulae are presented for both species.

Organogénie florale des genres Culcasia et Cercestis (Araceae)

1996 ◽  
Vol 74 (6) ◽  
pp. 898-908 ◽  
Author(s):  
Denis Barabé ◽  
Charles Bertrand
Keyword(s):  
Flower Development ◽  
Floral Development ◽  
Intermediate Zone ◽  
The Other ◽  
Other Hand ◽  
Unisexual Flowers ◽  
Male Flowers ◽  
Morphogenetic Gradient ◽  
Female Flowers

The floral development of Culcasia saxatilis, Culcasia tenuifolia, and Cercestis stigmaticus has been analyzed. These two genera possess unisexual flowers without perianth. In these species, the cylindrical inflorescence carry male flowers in the upper part and female flowers in the lower part. In C. tenuifolia, the separation between the female zone and the male zone is very sharp. There is no intermediate zone. In C. saxatilis and C. stigmaticus, we may observe rudimentary bisexual flowers between the two zones. In this intermediate zone, flowers located near the male zone possess male appendages more developped than those located near the female zone. On the other hand, the flowers located near the female zone possess female appendages more developped than those located near the male zone. The results suggest the existence of a morphogenetic gradient in the inflorescence of some species of Araceae. Keywords: morphogenesis, gradient, flower, development, inflorescence.

Floral structure and development in the dioecious Australian endemic Lomandra longifolia (Lomandraceae)

2008 ◽  
Vol 56 (8) ◽  
pp. 666 ◽  
Author(s):  
Nabil M. Ahmad ◽  
Peter M. Martin ◽  
John M. Vella
Keyword(s):  
Floral Development ◽  
Cytological Analysis ◽  
Floral Structure ◽  
Male And Female ◽  
Pistil Abortion ◽  
Stamen Arrest ◽  
Male Flowers ◽  
Mother Cells ◽  
Female Flowers ◽  
Scanning Electron

The micromorphology and histology of the development of male and female flowers of the dioecious Australian endemic species Lomandra longifolia Labill. was studied by means of scanning electron microscopy and light microscopy of entire and sectioned material. Although mature flowers are functionally unisexual, in the early stages of development pistillate and staminate flowers are identical and apparently bisexual. In a sequential fashion, six perianth parts are initiated within two alternating whorls, the sepals first and the petals second; six stamens are initiated in two alternating whorls of three stamens each, the first opposite the sepals and the second opposite the petals; and last, a central gynoecium is initiated. Following initiation, the two flower types diverge developmentally when the stamens become bilobed. In male flowers, cytological analysis of the slowly growing abortive pistil shows that megasporogenesis does not occur. Pistil abortion happens before meiosis whereas the stamens continue to develop until maturity and dehiscence. In female flowers, stamen arrest occurs before the onset of meiosis in microspore mother cells, after which the pistil continues its development through megasporogenesis and megagametogenesis. In all, 14 stages of floral development of both male and female flowers have been designated. Stages 1–6 of the two flower types were common to both sexes.

Studies in the Alismataceae. XI. Development of the inflorescence and flowers of Wiesneria triandra (Dalzell) Micheli

2000 ◽  
Vol 77 (11) ◽  
pp. 1569-1579
Author(s):  
W A Charlton
Keyword(s):  
Shoot Development ◽  
Annual Plant ◽  
Foliage Leaf ◽  
The Family ◽  
Unisexual Flowers ◽  
Male Flowers ◽  
Female Flowers

Wiesneria triandra (Dalzell) Micheli is an unusual annual plant of the Alismataceae with spike-like inflorescences bearing unisexual flowers. Shoot development follows the sympodial pattern of other Alismataceae, but the cycle is so condensed that initiation of each foliage leaf is followed by inflorescence formation. The plant develops a tufted habit by the formation of an unusual accesory bud adjacent to each inflorescence. Male flowers have three sepals, three petals, three stamens, and usually three carpellodes; female flowers have a similar perianth, three staminodes, and three or more carpels. Up to the first three carpels, floral parts are arranged in alternating trimerous whorls. Additional carpels may occur above and between those of the first whorl. The androecium is particularly unusual for the Alismataceae since it has conventional alternation of stamens with petals rather than the antipetalous pairs of stamens commonly perceived in the family, but the phylogenetic postion of Wiesneria within the family (as revealed by other studies) indicates that the apparently conventional androecium of Wiesneria represents a derived state rather than a primitive one. The unisexual flowers also represent a derived state.

Pollination ecology of Monstera obliqua (Araceae) in French Guiana

2007 ◽  
Vol 23 (5) ◽  
pp. 607-610 ◽  
Author(s):  
Mathieu Chouteau ◽  
Melanie McClure ◽  
Marc Gibernau
Keyword(s):  
French Guiana ◽  
Pollination Ecology ◽  
Lower Portion ◽  
Floral Rewards ◽  
Pollination Mechanisms ◽  
Unisexual Flowers ◽  
Male Flowers ◽  
Female Flowers

Data on pollination ecology of Araceae are still scarce and most concern species belonging to the subfamily Aroideae (García-Robledo et al. 2004, Gibernau 2003, Ivancic et al. 2004, 2005; Maia & Schlindwein 2006). In this subfamily, inflorescences consist of unisexual flowers: female flowers are located in the lower portion and the male flowers are in the upper portion of the inflorescence (Mayo et al. 1997). In the documented neotropical Aroideae, pollinators are nocturnal beetles and pollination mechanisms take place within a floral chamber during a short flowering cycle (generally 24–48 h) with floral rewards (sterile flowers rich in proteins and/or lipids) for the beetle pollinators, the secretion of resin to secure pollen on the pollinator, and the production of heat and odours (Chouteau et al. 2007, García-Robledo et al. 2004, Gibernau & Barabé 2002, Gibernau et al. 1999, 2000, 2003; Maia & Schlindwein 2006, Young 1986).

Differential nectar production between male and female flowers in a wild cucurbit: Cucurbita maxima ssp. andreana (Cucurbitaceae)

2002 ◽  
Vol 80 (11) ◽  
pp. 1203-1208 ◽  
Author(s):  
Lorena Ashworth ◽  
Leonardo Galetto
Keyword(s):  
Reproductive Output ◽  
Male Flower ◽  
Female Flower ◽  
Cucurbita Maxima ◽  
Nectar Production ◽  
Male And Female ◽  
Nectar Sugar Composition ◽  
Nectar Sugar ◽  
Male Flowers ◽  
Female Flowers

In dioecious and monoecious plants that depend on animal vectors for reproduction, pollinators have to be attracted to male and female flowers for pollination to be effective. In the monoecious Cucurbita maxima ssp. andreana, male flowers are produced in greater quantity, are spatially more exposed to pollinators and offer pollen in addition to nectar as floral rewards. Nectar traits were compared between male and female flowers to determine any differences in the characteristics of the main reward offered to pollinators. Nectar chemical composition and sugar proportions were similar between flower types. Total nectar sugar production per female flower was threefold higher than per male flower, and nectar removal did not have any effect on total nectar production in both flower morphs. Pollinators reduced nectar standing crops to similar and very scarce amounts in both flower types. Results indicate indirectly that pollinators are consuming more nectar from female flowers, suggesting that the higher nectar production in female flowers may be a reward-based strategy to achieve the high female reproductive output observed in this species.Key words: Cucurbitaceae, Cucurbita maxima ssp. andreana, nectar production, nectar sugar composition, removal effects, standing crop.

scholarly journals The Effects of Silver Nitrate Applications on the Flower Quantity of Cucumbers (Cucumis sativus L.)

2011 ◽  
Vol 39 (1) ◽  
pp. 139 ◽  
Author(s):  
Deniz KARAKAYA ◽  
Hüseyin PADEM
Keyword(s):  
Silver Nitrate ◽  
Cucumis Sativus ◽  
Male Flower ◽  
Flower Formation ◽  
Cucumis Sativus L ◽  
Male Flowers ◽  
Female Flowers

This study was conducted to investigate the effects of silver nitrate (AgNO3) on the flower quantity of cucumbers. The seeds used in this study, which was carried out in a plastic greenhouse, in the Gazi village of Antalya Province (Turkey) the during spring and autumn 2005 breeding periods, were ‘Mostar F1’ (designated as ‘GND1’) and ‘Vesco Seeds Beith Alpha F1 (26.50 F1)’, designated as ‘GND2’ and those are the types having common production. The silver nitrate application was performed by the method of spraying on the growth tips of plants and 0, 250, 500, 750, and 1000 ppm silver nitrate doses were administered. The research was conducted with 4 repetitions having 5 plants in each repetition according to the Random Parcel Trial Pattern. In order to determine the effects of the applications, the effects of a number of female flowers and male flowers on generative characteristics of planting periods (spring and fall) were identified and the results were statistically evaluated. According to the results obtained in this research, AgNO3 has led to the formation of male flowers (no male flower formation in control), has increased the number of male flowers, and has led to a decrease in the number of female flowers. The increase in the number of male flowers varied according to the periods (in ‘GND2’).

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.

scholarly journals Pollen load and distribution on the body of Elaeidobius kamerunicus Faust. (Coleoptera: Curculionidae) within oil palm plantations

2020 ◽  
Vol 17 (2) ◽  
pp. 81
Author(s):  
Van Basten Tambunan ◽  
Bandung Sahari ◽  
Damayanti Buchori ◽  
Purnama Hidayat
Keyword(s):  
Oil Palm ◽  
The Body ◽  
Body Parts ◽  
Pollen Load ◽  
Male And Female ◽  
Male Flowers ◽  
Pollen Distribution ◽  
Male To Female ◽  
Female Flowers ◽  
Elaeidobius Kamerunicus

<p>The African oil palm weevil,<strong> </strong><em>Elaeidobius kamerunicus</em> is an effective pollinator of oil palm. Each individual palm produces exclusively male or female inflorescence so that the success of pollination depends on the ability of the pollinator to transfer pollen from male to female flowers. The objective of this research was to study the amount of pollen carried by <em>E. kamerunicus</em> between male and female inflorescences (pollen load) and the amount of pollen carried on each part of the weevil’s body (pollen distribution). Fifty each of male and female  <em>E. kamerunicus</em> individuals were collected from male and female flowers on trees in 3 locations: Siantar (North Sumatra), Dramaga (West Java), and Morowali (Central Sulawesi). Data on pollen load and pollen distribution on the weevil’s body were analyzed using <em>ImageJ</em> software. Results show that <em>E. kamerunicus</em> individuals collected more pollen from male flowers than from female flowers. In addition, male insects carried more pollen on their bodies than female insects. Pollen distribution on weevil body parts was highest on the elytra, followed by the thorax, abdomen, legs, and head respectively.</p>

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