Ontogeny of floral organs and morphology of floral apex in Phellodendron amurense (Rutaceae)

2002 ◽  
Vol 50 (5) ◽  
pp. 633 ◽  
Author(s):  
Qingyuan Zhou ◽  
Yinzheng Wang ◽  
Xiaobai Jin
Keyword(s):  
Laser Scanning ◽  
Male Flower ◽  
Female Flower ◽  
Laser Scanning Confocal Microscopy ◽  
Morphological Evidence ◽  
Phellodendron Amurense ◽  
Flower Buds ◽  
Floral Organs ◽  
Floral Apex ◽  
Female Flowers

The ontogeny of floral organs and the morphology of floral apex in the dioecious Phellodendron amurense Rupr. were investigated by light microscopy (LM), scanning electron microscopy (SEM) and laser scanning confocal microscopy (LSCM). Investigations indicated that P. amurense is hermaphroditic in its organisation and a common set of floral organs (sepals, petals, stamens and carpels) arise in all flowers during the early stages of development. Later, selective abortion of gynoecium and androecium occurs resulting in dimorphic unisexual flowers. The carpels in male flower buds become different from those in female flower buds soon after their initiation. The stamens of female flowers are not differentiated into anthers and filaments before abortion. The poorly differentiated carpel of male flowers never develops normal structures. Floral morphological evidence supports that Zanthoxylum, Tetradium and Phellodendron are related to one another in a linear sequence. LSCM revealed some interesting features on the apical meristem surface such as zonal differentiation, a triangular or sectorial cell, radiating cell files and linear rows of anticlinal cell walls fluorescing relatively brightly. The concept of carpel-enhancing meristem in the floral apex is tentatively proposed to account for the different fates of carpel development in male and female flowers in P. amurense.

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 growth of flower bud, life history, and population structure of Rafflesia arnoldii (Rafflesiaceae) in Bengkulu, Sumatra, Indonesia

2020 ◽  
Vol 21 (2) ◽  
Author(s):  
AGUS SUSATYA
Keyword(s):  
Population Structure ◽  
Life History ◽  
Male Flower ◽  
Female Flower ◽  
Exponential Model ◽  
Flower Buds ◽  
Flower Bud ◽  
Dynamics Of Population ◽  
History Of ◽  
Two Populations

Abstract. Susatya A. 2020. The growth of flower bud, life history, and population structure of Rafflesia arnoldii (Rafflesiaceae) in Bengkulu, Sumatra, Indonesia. Biodiversitas 21: 792-798. The life history of Rafflesia arnoldii R.Br. is the reflection of the complex interaction between flower bud development and the external environments in order to reach its optimal survivorship. The objectives of the study were to determine the growth of flower buds at various development stages, to reconstruct the life history, and to know the population structure of R. arnoldii. The study was carried out at Taba Penanjung, Bengkulu Province, Indonesia. Two populations consisting of 17 individual buds of R. arnoldii were selected for the research. All buds were categorized into six visible stages, mapped, measured their diameters, and recorded their fates every two weeks for six months. The exponential model of growth development was applied to reconstruct the life history. The results showed that buds from the perigone stage respectively grew 3.5 and 12 times faster than those from the bract and cupule stages. The exponential growth of flower bud was confirmed, and explained by Y = 0.785 e0.0052 X, where Y and X were respectively diameter and age of flower bud. The complete life history of R. arnoldii required 3.5 to 5 years, where a female flower needed a longer time than a male flower. The population structure of R. arnoldii was not constant, but changed dynamically over time. The dynamics of population structure was mainly caused by the high mortality of small buds and the low flower bud recruitment.

scholarly journals Transcriptome-based analysis of the hormone regulation mechanism of gender differentiation in Juglans mandshurica Maxim

PeerJ ◽  
2021 ◽  
Vol 9 ◽  
pp. e12328
Author(s):  
Baiting Qin ◽  
Xiujun Lu ◽  
Xiaomei Sun ◽  
Jianguo Cui ◽  
Jifeng Deng ◽  
...  
Keyword(s):  
Signal Transduction ◽  
Female Flower ◽  
Negative Regulator ◽  
Regulation Mechanism ◽  
Juglans Mandshurica ◽  
Flower Buds ◽  
Male And Female ◽  
Gender Differentiation ◽  
Male Flowers ◽  
Female Flowers

Juglans mandshurica Maxim is a hermaphroditic plant belonging to the genus Juglans in the family Juglandaceae. The pollination period of female flowers is different from the loose powder period of male flowers on the same tree. In several trees, female flowers bloom first, whereas in others, male flowers bloom first. In this study, male and female flower buds of J. mandshurica at the physiological differentiation stage were used. Illumina-based transcriptome sequencing was performed, and the quality of the sequencing results was evaluated and analyzed. A total of 138,138 unigenes with an average length of 788 bp were obtained. There were 8,116 differentially expressed genes (DEGs); 2,840 genes were upregulated, and 5,276 genes were downregulated. The DEGs were classified by Gene Ontology and analyzed by Kyoto Encyclopedia of Genes and Genomes. The signal transduction factors involved in phytohormone synthesis were selected. The results displayed that ARF and SAUR were expressed differently in the auxin signaling pathway. Additionally, DELLA protein (a negative regulator of gibberellin), the cytokinin synthesis pathway, and A-ARR were downregulated. On April 2nd, the contents of IAA, GA, CTK, ETH and SA in male and female flower buds of two types of J. mandshurica were opposite, and there were obvious genes regulating gender differentiation. Overall, we found that the sex differentiation of J. mandshurica was related to various hormone signal transduction pathways, and hormone signal transduction plays a leading role in regulation.

Floral development of Comptonia peregrina (Myricaceae)

1974 ◽  
Vol 52 (10) ◽  
pp. 2165-2169 ◽  
Author(s):  
Alastair D. Macdonald
Keyword(s):  
Floral Development ◽  
Early Stage ◽  
Male Flower ◽  
Female Flower ◽  
Median Plane ◽  
Distal Portion ◽  
Second Order ◽  
Third Order ◽  
Floral Apex ◽  
Growth Activity

Early stages of development of the male and female flower are similar; two second-order bracts arise in the transversal plane on either side of the floral apex before the apex flattens and becomes somewhat concave because of growth activity at the flank of the apex. In the female flower, the gynoecium develops as an extension of the girdling gynoecial primordium and the two primordial stigmas each result from more rapid growth in the median plane at the distal portion of the gynoecial wall. The floral apex resumes growth to form the unitegmic ovule. Third-order lanceolate-shaped bracts develop from a meristem situated in the axil of each second-order bract. In the male flower, staminate primordia arise at three or four loci on the ridge surrounding the apex. The apex briefly resumes growth. Growth of the second-order bracts terminates at an early stage. The floral construction is compared to other myricaceous species. It is concluded that the axillary scale-like bracts of the female flower are third-order bracts; the gynoecium does not overtop the second-order axis and the female flower is not a reduced cyme; the male flower is more floral- than inflorescence-like compared to some other myricaceous species.

scholarly journals Inflorescence morphology and development of suweg (Amorphophallus paeoniifolius (Dennst.) Nicolson

2020 ◽  
Vol 21 (12) ◽  
Author(s):  
TRI HANDAYANI ◽  
YUZAMMI ◽  
JULISASI TRI HADIAH
Keyword(s):  
Male Flower ◽  
Female Flower ◽  
Lucilia Sericata ◽  
Male And Female ◽  
Inflorescence Morphology ◽  
Bud Emergence ◽  
Insect Visitors ◽  
Female Flowers ◽  
Flowering Process

Abstract. Hanfayani T, Yuzammi, Hadiah JT. 2020. Inflorescence morphology and development of suweg (Amorphophallus paeoniifolius (Dennst.) Nicolson. Biodiversitas 21: 5835-5844. Inflorescence of Amorphophallus paeoniifolius (Dennst.) Nicolson consists of two main parts: spathe and spadix. Detailed information on its development, however, is not yet available. This study aimed to investigate the development and morphology of suweg’s inflorescence, to reveal the anthesis of male and female flowers, and to observe its insect visitors. The study observed 46 inflorescences, ten of which were measured for detailed developments. Inflorescences were observed from bud emergence to withering during one flowering cycle. The results showed that the flowering process included six phases which altogether required 22 to 36 days, namely the developments of inflorescence bud, cataphyll, spathe and spadix, appendix, fully bloomed inflorescence, and flowers anthesis. The inflorescence height including peduncle was 48–75 cm, spathe 19–50 cm long, spathe circle 65–176 cm, appendix 13–33 cm long, and appendix circle 45–80 cm. Three appendix forms were observed: ovate (43.48%), triangular conic (41.30%), and rounded (15.22%). Female flower anthesis occurred one day prior to male flower anthesis. Insect visitors found during anthesis were Lucilia sericata (Calliphoridae), Sarcophaga sp. (Sarcophagidae), and Trigona speciosa (Apidae).

scholarly journals Ethephon Treatment May Alleviate the Suppression of Female Flowers of Cucurbita Pepo under High Temperatures

HortScience ◽  
2006 ◽  
Vol 41 (6) ◽  
pp. 1421-1422 ◽  
Author(s):  
H.C. Wien
Keyword(s):  
High Temperature ◽  
High Temperatures ◽  
Elevated Temperatures ◽  
Female Flower ◽  
Flower Buds ◽  
Flower Bud ◽  
Ethylene Action ◽  
Ethephon Treatment ◽  
Flower Bud Formation ◽  
Female Flowers

When pumpkins are grown in elevated temperatures (32/27 °C day/night) for 1 week during flower development, fewer female flower buds are formed than at normal temperatures (20/15 °C) and only a small percentage of these reach anthesis. To determine if application of the ethylene-releasing compound ethephon can overcome the suppression of female flowers at high temperatures, `Baby Bear' pumpkin plants were sprayed at the two-leaf stage with 100 or 300 μL L–1 ethephon and then grown in hot and cool greenhouse compartments. At 20/15 °C, 17% of the first 15 main stem nodes produced female flower buds on control plants and virtually all of these developed into open flowers. The higher rate of ethephon increased female bud percentage to 37%. At 32/27 °C, only 3% of the nodes formed female flower buds and 2% flowered. Application of ethephon did not significantly increase female expression at high temperature, and none of the buds reached anthesis. Treatment with the inhibitor of ethylene action silver thiosulfate reduced female flower bud formation at the low temperature and entirely suppressed female flower buds at high temperature. In two additional experiments, these treatments were applied to two cultivars grown at a less extreme 32/20 and at 20/15 °C. Female buds and open flowers were moderately increased by ethephon in the high temperatures, suggesting that ethephon might foster female flowering in less extreme temperatures. Further work is needed to determine if ethephon treatment can overcome the heat-induced inhibition of female flowers in pumpkin under field conditions.

scholarly journals Detecting the Candidate Gender Determinants by Bioinformatic Prediction of miRNAs and Their Targets from Transcriptome Sequences of the Male and Female Flowers in Salix suchowensis

2017 ◽  
Vol 2017 ◽  
pp. 1-9
Author(s):  
Suyun Wei ◽  
Ning Ye ◽  
Tongming Yin
Keyword(s):  
Expressed Sequence Tags ◽  
Target Genes ◽  
Male Flower ◽  
Female Flower ◽  
Flower Buds ◽  
Regulate Gene Expression ◽  
Male And Female ◽  
Sequence Complementarity ◽  
Expressed Sequence ◽  
Posttranscriptional Level

MicroRNAs (miRNAs) belong to a class of small, noncoding, and endogenous single-stranded RNAs that negatively regulate gene expression at the posttranscriptional level. Potential miRNAs can be identified based on sequence homology since miRNAs are highly conserved in plants. In this study, we aligned the expressed sequence tags derived from flower buds of male and female S. suchowensis to miRNAs in the miRBase, which enable us to identify 34 potential miRNAs from flower buds of the alternate sexes. Among them, 11 were from the female and 23 were from the male. Analyzing sequence complementarity led to identification of 124 and 55 miRNA targets in the male and female flower buds, respectively. By mapping the target genes of the predicted miRNAs to the sequence assemblies of S. suchowensis, a miR156 mediated gene was detected at the gender locus of willow, which was a transcription factor involved in flower development. It is noteworthy that this target is not expressed in male flower, while it is expressed fairly highly in female flower based on the transcriptome data derived from the alternate sexes of willows. This study provides new bioinformatic clue for further exploring the genetic mechanism underlying gender determination in willows.

Development of the inflorescence and flower of Sagittaria cuneata

1977 ◽  
Vol 55 (9) ◽  
pp. 1087-1105 ◽  
Author(s):  
V. Singh ◽  
R. Sattler
Keyword(s):  
Male Flower ◽  
Female Flower ◽  
Point Of View ◽  
Stamen Primordia ◽  
Tunica Layer ◽  
Mature Flower ◽  
Floral Apex ◽  
Developmental Point ◽  
Floral Bud ◽  
Developmental Modification

The reproductive region of Sagittaria cuneata is basically trimerous. This trimery is exhibited in the arrangement of the bracts, sepals, petals, pairs of stamens in the male flower, and pairs of staminodia in the female flower. In the male flower after the inception of three sepal primordia, each of the three petal primordia arises with one pair of stamen primordia on an alternisepalous bulge of the floral apex, i.e., a petal–stamen (CA) primordium. Subsequent stamen primordia are formed in alternation with the six first-formed primordia. If, for convenience sake, the first six primordia are referred to as the first whorl of stamens up to four additional whorls may be produced. Depending on the size of the floral bud, the third and fourth whorls (if present) consist of two to six stamen primordia, whereas the fifth whorl (if present) contains one to five stamen primordia. Finally, primordia of pistillodes are formed in varying numbers. In the female flower the presence of CA primordia could not be as clearly established as in the male flower. However, again each petal primordium is definitely associated with a pair of antepetalous primordia. The latter primordia develop into staminodia. In alternation with the first six staminodia six additional staminodia are formed and then again in alternation many whorls of pistils (carpels). Even in the mature flower the basic trimery is reflected in the triangular shape of the globose and massive gynoecium. From a developmental point of view, the male and female flowers are primarily trimerous. The polyandric androecium and the large pleiomerous gynoecium are superimposed on the primary trimery. It appears quite possible that this developmental modification also reflects a phylogenetic derivation. This means that the pleiomerous gynoecium and androecium are not primitive but rather advanced. There is no indication of a spiral arrangement of stamens and carpels.Whereas the foliage leaves, bracts, and sepals are initiated as dorsiventral primordia, the petals, stamens, staminodia, pistils, and pistillodes arise as more or less hemispherical mounds and become dorsiventral thereafter. The vegetative apices, inflorescence apices and the floral apices have a two-layered tunica over a massive corpus. Foliage leaves, bracts, sepals, petals, stamens, staminodia, carpels, and pistillodes are initiated by periclinal divisions in the second tunica layer. In the case of the stamens and staminodia the corpus may also contribute. Ovules are initiated by periclinal divisions of the second layer of the carpel primordium.

Five-Dimensional Microscopy using Widefield-Deconvolution: Practical Considerations and Biological Applications

1996 ◽  
Vol 54 ◽  
pp. 268-269
Author(s):  
W.F. Marshall ◽  
K. Oegema ◽  
J. Nunnari ◽  
A.F. Straight ◽  
D.A. Agard ◽  
...  
Keyword(s):  
Confocal Microscopy ◽  
High Speed ◽  
Laser Scanning ◽  
Ccd Camera ◽  
Image Plane ◽  
Time Lapse ◽  
Laser Scanning Confocal Microscopy ◽  
Three Dimensions ◽  
Excitation Light ◽  
Cooled Ccd

The ability to image cells in three dimensions has brought about a revolution in biological microscopy, enabling many questions to be asked which would be inaccessible without this capability. There are currently two major methods of three dimensional microscopy: laser-scanning confocal microscopy and widefield-deconvolution microscopy. The method of widefield-deconvolution uses a cooled CCD to acquire images from a standard widefield microscope, and then computationally removes out of focus blur. Using such a scheme, it is easy to acquire time-lapse 3D images of living cells without killing them, and to do so for multiple wavelengths (using computer-controlled filter wheels). Thus, it is now not only feasible, but routine, to perform five dimensional microscopy (three spatial dimensions, plus time, plus wavelength).Widefield-deconvolution has several advantages over confocal microscopy. The two main advantages are high speed of acquisition (because there is no scanning, a single optical section is acquired at a time by using a cooled CCD camera) and the use of low excitation light levels Excitation intensity can be much lower than in a confocal microscope for three reasons: 1) longer exposures can be taken since the entire 512x512 image plane is acquired in parallel, so that dwell time is not an issue, 2) the higher quantum efficiently of a CCD detect over those typically used in confocal microscopy (although this is expected to change due to advances in confocal detector technology), and 3) because no pinhole is used to reject light, a much larger fraction of the emitted light is collected. Thus we can typically acquire images with thousands of photons per pixel using a mercury lamp, instead of a laser, for illumination. The use of low excitation light is critical for living samples, and also reduces bleaching. The high speed of widefield microscopy is also essential for time-lapse 3D microscopy, since one must acquire images quickly enough to resolve interesting events.

Laser Scanning Confocal Microscopy and Three-Dimesnsional Reconstruction of the Mitotic Spindles of Unequally Dividing Embryonic Cells

1990 ◽  
Vol 48 (3) ◽  
pp. 166-167
Author(s):  
J. Holy ◽  
G. Schatten
Keyword(s):  
Confocal Microscopy ◽  
Mitotic Spindle ◽  
Laser Scanning ◽  
Three Dimensional ◽  
Laser Scanning Confocal Microscopy ◽  
Two Dimensions ◽  
Embryonic Cells ◽  
Mitotic Spindles ◽  
Cleavage Division ◽  
Scanning Confocal Microscopy

One of the classic limitations of light microscopy has been the fact that three dimensional biological events could only be visualized in two dimensions. Recently, this shortcoming has been overcome by combining the technologies of laser scanning confocal microscopy (LSCM) and computer processing of microscopical data by volume rendering methods. We have employed these techniques to examine morphogenetic events characterizing early development of sea urchin embryos. Specifically, the fourth cleavage division was examined because it is at this point that the first morphological signs of cell differentiation appear, manifested in the production of macromeres and micromeres by unequally dividing vegetal blastomeres.The mitotic spindle within vegetal blastomeres undergoing unequal cleavage are highly polarized and develop specialized, flattened asters toward the micromere pole. In order to reconstruct the three-dimensional features of these spindles, both isolated spindles and intact, extracted embryos were fluorescently labeled with antibodies directed against either centrosomes or tubulin.

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