Unicarpellate floral development in Potamogeton zosteriformis

1981 ◽  
Vol 59 (4) ◽  
pp. 495-504 ◽  
Author(s):  
U. Posluszny
Keyword(s):  
Floral Development ◽  
Floral Meristem ◽  
Central Portion ◽  
Points Of View ◽  
Stamen Pairs

Floral development in the species Potamogeton zosteriformis is compared with that of other species of Potamogeton previously investigated (P. densus and P. richardsonii). A spike inflorescence is found on which 6 to 20 flowers develop. These flowers develop their appendages acropetally; first, the four tepals are initiated followed by the four stamens opposite the tepals. As in the flower of P. densus, the two lateral stamens are each initiated as two separate primordia. Unlike any other Potamogeton species where four carpels generally arise, alternating with the tepal and stamen pairs, in P. zosteriformis a single carpel consistently develops on the central portion of the remaining floral meristem. Histological preparations did not reveal any vestigial procambial strands differentiating in the gynoecium. This unique floral development is examined from several points of view. Morphogenetic comparisons are made with other species of Potamogeton which develop tetramerous gynoecia. Morphologically the nature of the Potamogeton flower is reexamined and phylogenetically the possibility of P. zosteriformis as a link or transition between the bisexual and unisexual groups within the Najadales is considered.

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 SlGT11 Controls Floral Organ Patterning and Floral Determinacy in Tomato

2020 ◽  
Author(s):  
Liling Yang ◽  
Shilian Qi ◽  
Arfa touqeer ◽  
Haiyang Li ◽  
Xiaolan Zhang ◽  
...  
Keyword(s):  
Floral Development ◽  
Bulked Segregant Analysis ◽  
Floral Organ ◽  
Fruit Production ◽  
Floral Meristem ◽  
Rnai Silencing ◽  
The Third ◽  
Spatiotemporal Expression ◽  
Higher Temperature ◽  
Floral Determinacy

Abstract Background: Flower development directly affects fruit production in tomato. Despite the framework mediated by ABC genes have been established in Arabidopsis, the spatiotemporal precision of floral development in tomato has not been well examined.Results: Here, we analyzed a novel tomato stamenless like flower (slf) mutant in which the development of stamens and carpels is disturbed, with carpelloid structure formed in the third whorl and ectopic formation of floral and shoot apical meristem in the fourth whorl. Using bulked segregant analysis (BSA), we assigned the causal mutation to the gene Solanum lycopersicum GT11 (SlGT11) that encodes a transcription factor belonging to Trihelix gene family. SlGT11 is expressed in the early stages of the flower and the expression becomes more specific to the primordium position corresponding to stamens and carpels in later stages of the floral development. Further RNAi silencing of SlGT11 verifies the defective phenotypes of the slf mutant. The carpelloid stamen in slf mutant indicates that SlGT11 is required for B-function activity in the third whorl. The failed termination of floral meristem and the occurrence of floral reversion in slf indicate that part of the C-function requires SlGT11 activity in the fourth whorl. Furthermore, we find that at higher temperature, the defects of slf mutant are substantially enhanced, with petals transformed into sepals, all stamens disappeared, and the frequency of ectopic shoot/floral meristem in fourth whorl increased, indicating that SlGT11 functions in the development of the three inner floral whorls. Consistent with the observed phenotypes, it was found that B, C and an E-type MADS-box genes were in part down regulated in slf mutants.Conclusions: Together with the spatiotemporal expression pattern, we suggest that SlGT11 functions in floral organ patterning and maintenance of floral determinacy in tomato.

Floral development of Rosa setigera

1993 ◽  
Vol 71 (1) ◽  
pp. 74-86 ◽  
Author(s):  
James R. Kemp ◽  
Usher Posluszny ◽  
Jean M. Gerrath ◽  
Peter G. Kevan
Keyword(s):  
Key Words ◽  
Floral Development ◽  
Functional Approach ◽  
Floral Meristem ◽  
Cryptic Dioecy ◽  
Congenital Fusion ◽  
Postgenital Fusion

The development of the flower of Rosa setigera from initiation to the onset of anthesis is described. Rosa setigera is the only known member of the genus Rosa to exhibit dioecy. Flowers of functionally staminate (male) and functionally carpellate (female) plants appear identical, a condition referred to as cryptic dioecy. Discrete sepals and petals are formed on the floral meristem. As the hypanthium forms, stamens are initiated in alternating whorls on the wall of the hypanthium and continue to develop as the hypanthium extends. Carpel primordia arise individually on the remainder of the floral meristem and show neither adnation to the hypanthial wall nor coalescence to one another as they give rise to the styles and stigmas that are exserted above the hypanthium lip. The only observable fusion in this species appears to be the postgenital fusion of the margins of the carpel primordia to form the enclosed locule. Although historically the hypanthium has been variously interpreted as either axial and (or) appendicular in nature, resulting from congenital fusion of sepals, petals, and stamens, this paper uses a more realistic, testable and functional approach to the development of the hypanthium that is in keeping with current concepts such as process morphology. Key words: Rosa setigera, dioecy, floral development, fusion, hypanthium.

scholarly journals SlGT11 controls floral organ patterning and floral determinacy in tomato

2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Liling Yang ◽  
Shilian Qi ◽  
Arfa Touqeer ◽  
Haiyang Li ◽  
Xiaolan Zhang ◽  
...  
Keyword(s):  
Floral Development ◽  
Bulked Segregant Analysis ◽  
Floral Organ ◽  
Fruit Production ◽  
Floral Meristem ◽  
Rnai Silencing ◽  
The Third ◽  
Spatiotemporal Expression ◽  
Higher Temperature ◽  
Floral Determinacy

Abstract Background Flower development directly affects fruit production in tomato. Despite the framework mediated by ABC genes have been established in Arabidopsis, the spatiotemporal precision of floral development in tomato has not been well examined. Results Here, we analyzed a novel tomato stamenless like flower (slf) mutant in which the development of stamens and carpels is disturbed, with carpelloid structure formed in the third whorl and ectopic formation of floral and shoot apical meristem in the fourth whorl. Using bulked segregant analysis (BSA), we assigned the causal mutation to the gene Solanum lycopersicum GT11 (SlGT11) that encodes a transcription factor belonging to Trihelix gene family. SlGT11 is expressed in the early stages of the flower and the expression becomes more specific to the primordium position corresponding to stamens and carpels in later stages of the floral development. Further RNAi silencing of SlGT11 verifies the defective phenotypes of the slf mutant. The carpelloid stamen in slf mutant indicates that SlGT11 is required for B-function activity in the third whorl. The failed termination of floral meristem and the occurrence of floral reversion in slf indicate that part of the C-function requires SlGT11 activity in the fourth whorl. Furthermore, we find that at higher temperature, the defects of slf mutant are substantially enhanced, with petals transformed into sepals, all stamens disappeared, and the frequency of ectopic shoot/floral meristem in fourth whorl increased, indicating that SlGT11 functions in the development of the three inner floral whorls. Consistent with the observed phenotypes, it was found that B, C and an E-type MADS-box genes were in part down regulated in slf mutants. Conclusions Together with the spatiotemporal expression pattern, we suggest that SlGT11 functions in floral organ patterning and maintenance of floral determinacy in tomato.

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.

Studies in the Alismataceae. XII. Floral organogenesis in Damasonium alisma and Baldellia ranunculoides, and comparisons with Butomus umbellatus

2004 ◽  
Vol 82 (4) ◽  
pp. 528-539 ◽  
Author(s):  
W A Charlton
Keyword(s):  
Floral Development ◽  
De Novo ◽  
Fundamental Feature ◽  
Floral Organogenesis ◽  
General Plan ◽  
Stamen Pairs

Floral organogenesis of Damasonium alisma Mill. occurs at first in an alternating trimerous pattern typical of Alismataceae, with the formation of three sepals, then three bulges, corresponding to the CA (common perianth–androecium) primordia described in some other Alismataceae, alternating with the sepals. A petal is initiated on each bulge, and a pair of stamens is initiated either on or close to it. Three carpels are initiated in positions alternating with the petals and stamen pairs, and three further carpels then arise above and between the first three. At maturity and in fruit the carpels lie in a whorled arrangement. Floral development in Baldellia ranunculoides (L.) Parl. is identical up to the initiation of the six stamens. After this, six carpel primordia are formed alternating with the stamens, and further carpel primordia arise alternating with those previously formed. In Butomus, up to the initiation of the first six stamens, the general plan of development resembles that of the two Alismataceae. Three further whorls of organs arise in alternation: a whorl of three stamens arises over the stamen pairs followed by two whorls each of three carpel primordia. It is argued that the trimerous appearance of the whorl of sepals (or outer perianth in Butomus) arises de novo and represents a genuine expression of trimery. However, most of the subsequent features of development in these flowers can be seen as arising from phyllotactic mechanisms that cause new primordia to arise between and above pre-existing ones. Consequently the appearance of trimerous or hexamerous whorls above the first whorl of perianth does not represent a fundamental feature of development. The nature of variations in the positional relationships of inner perianth, stamen, and carpel primordia in various Alismataceae and Butomus strengthen the case that there is a significant developmental association between inner perianth members and associated pairs of stamens, which may be connected with the evolution of the flowers from pseudanthial structures.Key words: Baldellia, Butomus, Damasonium, Alismatidae, flower, organogenesis.

scholarly journals SlGT11 Controls Floral Organ P atterning and F loral Determinacy in Tomato

2020 ◽  
Author(s):  
Liling Yang ◽  
Shilian Qi ◽  
Arfa touqeer ◽  
Haiyang Li ◽  
Xiaolan Zhang ◽  
...  
Keyword(s):  
Floral Development ◽  
Bulked Segregant Analysis ◽  
Floral Organ ◽  
Fruit Production ◽  
Floral Meristem ◽  
Rnai Silencing ◽  
The Third ◽  
Spatiotemporal Expression ◽  
Higher Temperature ◽  
Type Gene

Abstract Background: Flower development directly affects fruit production in tomato. Despite the framework mediated by ABC genes have been established in Arabidopsis, the spatiotemporal precision of floral development in tomato has not been well examined.Results: Here, we analyzed a novel tomato stamenless like flower (slf) mutant in which the development of stamens and carpels is disturbed, with carpelloid structure formed in the third whorl and ectopic formation of floral and shoot apical meristem in the fourth whorl. Using bulked segregant analysis (BSA), we assigned the causal mutation to the gene Solanum lycopersicum GT11 (SlGT11) that encodes a transcription factor belonging to Trihelix gene family. SlGT11 is expressed in the early stages of the flower and the expression becomes more specific to the primordium position corresponding to stamens and carpels in later stages of the floral development. Further RNAi silencing of SlGT11 verifies the defective phenotypes of the slf mutant. The carpelloid stamen in slf mutant indicates that SlGT11 functions like as a B-type gene in the third whorl. The failed termination of floral meristem and the occurrence of floral reversion in slf indicate that SlGT11 also functions as a C-type gene in the fourth whorl. Furthermore, we find that at higher temperature, the defects of slf mutant are substantially enhanced, with petals transformed into sepals, all stamens disappeared, and the frequency of ectopic shoot/floral meristem in fourth whorl increased, indicating that SlGT11 may have the function of tomato B and E class gene in the development of second and fourth whorls.Conclusions: Together with the spatiotemporal expression pattern, we suggest that SlGT11 functions in floral organ patterning and maintenance of floral determinacy in tomato.

scholarly journals SlGT11 Controls Floral Organ Patterning and Floral Determinacy in Tomato

2020 ◽  
Author(s):  
Liling Yang ◽  
Shilian Qi ◽  
Arfa touqeer ◽  
Haiyang Li ◽  
Xiaolan Zhang ◽  
...  
Keyword(s):  
Floral Development ◽  
Bulked Segregant Analysis ◽  
Floral Organ ◽  
Fruit Production ◽  
Floral Meristem ◽  
Rnai Silencing ◽  
The Third ◽  
Spatiotemporal Expression ◽  
Higher Temperature ◽  
Floral Determinacy

Abstract Background: Flower development directly affects fruit production in tomato. Despite the framework mediated by ABC genes have been established in Arabidopsis, the spatiotemporal precision of floral development in tomato has not been well examined.Results: Here, we analyzed a novel tomato stamenless like flower (slf) mutant in which the development of stamens and carpels is disturbed, with carpelloid structure formed in the third whorl and ectopic formation of floral and shoot apical meristem in the fourth whorl. Using bulked segregant analysis (BSA), we assigned the causal mutation to the gene Solanum lycopersicum GT11 (SlGT11) that encodes a transcription factor belonging to Trihelix gene family. SlGT11 is expressed in the early stages of the flower and the expression becomes more specific to the primordium position corresponding to stamens and carpels in later stages of the floral development. Further RNAi silencing of SlGT11 verifies the defective phenotypes of the slf mutant. The carpelloid stamen in slf mutant indicates that SlGT11 is required for B-function activity in the third whorl. The failed termination of floral meristem and the occurrence of floral reversion in slf indicate that part of the C-function requires SlGT11 activity in the fourth whorl. Furthermore, we find that at higher temperature, the defects of slf mutant are substantially enhanced, with petals transformed into sepals, all stamens disappeared, and the frequency of ectopic shoot/floral meristem in fourth whorl increased, indicating that SlGT11 functions in the development of the three inner floral whorls. Consistent with the observed phenotypes, it was found that B, C and an E-type MADS-box genes were in part down regulated in slf mutants.Conclusions: Together with the spatiotemporal expression pattern, we suggest that SlGT11 functions in floral organ patterning and maintenance of floral determinacy in tomato.

Flower development in Amelanchier alnifolia (Maloideae)

1991 ◽  
Vol 69 (4) ◽  
pp. 844-857 ◽  
Author(s):  
Taylor A. Steeves ◽  
Margaret W. Steeves ◽  
A. Randall Olson
Keyword(s):  
Key Words ◽  
Flower Development ◽  
Floral Development ◽  
Floral Meristem ◽  
Amelanchier Alnifolia ◽  
Inferior Ovary ◽  
Postgenital Fusion

The development of the flower of Amelanchier alnifolia from initiation to the onset of anthesis is described. Sepals are formed sequentially, but interprimordial zonal growth results in the initiation of the hypanthium. Petals and stamens arise in whorls around the floral meristem as the hypanthium extends. They show neither coalescence nor adnation and do not appear to contribute to the development of the hypanthium. Gynoecial primordia arise individually, give rise to the styles and stigmas, and are joined basally by zonal growth to produce the roof of the ovary. The wall of the inferior ovary is interpreted as a gynoecial hypanthium. It is difficult to determine the extent to which the gynoecial primordia contribute to the development of the ovary. They do not give rise to most of its structure but may be responsible for the initiation of the ovules. There is evidence of postgenital fusion of the septal margins as they converge in the centre of the ovary. The timing of events in floral development is recorded for the locality of the study. The observations are discussed in relation to current theories concerning the nature of the inferior ovary. Key words: Amelanchier, flower, development, inferior ovary, hypanthium.

The induction and maintenance of flowering in Impatiens

Development ◽  
1997 ◽  
Vol 124 (17) ◽  
pp. 3343-3351 ◽  
Author(s):  
S. Pouteau ◽  
D. Nicholls ◽  
F. Tooke ◽  
E. Coen ◽  
N. Battey
Keyword(s):  
Transcriptional Activation ◽  
Flower Development ◽  
Vegetative Growth ◽  
Floral Development ◽  
Floral Meristem ◽  
Additional Function ◽  
Axillary Meristems ◽  
Meristem Identity ◽  
Floral Characters ◽  
Inductive Signal

The mechanisms that establish the floral meristem are now becoming clearer, but the way in which flowering is maintained is less well understood. Impatiens balsamina provides a unique opportunity to address this question because reversion to vegetative growth can be obtained in a predictable way by transferring plants from inductive to non-inductive conditions. Following increasing amounts of induction, reversion takes place at progressively later stages of flower development. Partial flower induction and defoliation experiments show that a floral signal is produced in the cotyledon in response to inductive conditions and that this signal progressively diminishes after transfer to non-inductive conditions, during reversion. Therefore reversion in Impatiens is most likely due to the failure of leaves to become permanent sources of inductive signal in addition to the lack of meristem commitment to flowering. Analysis of the expression of the Impatiens homologues of the meristem identity genes floricaula and squamosa indicates that a change in floricaula transcription is not associated with the establishment or maintenance of the floral meristem in this species. Squamosa transcription is associated with floral development and petal initiation, and is maintained in existing petal or petaloid primordia even after the meristem has reverted. However, it is not expressed in the reverted meristem, in which leaves are initiated in whorled phyllotaxis and without axillary meristems, both characteristics usually associated with the floral meristem. These observations show that squamosa expression is not needed for the maintenance of these floral characters. The requirement for the production of the floral signal in the leaf during the process of flower development may reflect an additional function separate to that of squamosa activation; alternatively the signal may be required to ensure continued transcriptional activation in the meristem.

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