scholarly journals Anatomy of ethylene-induced floral-organ abscission in Chamelaucium uncinatum (Myrtaceae)

2005 ◽  
Vol 53 (2) ◽  
pp. 119 ◽  
Author(s):  
Andrew J. Macnish ◽  
Donald E. Irving ◽  
Daryl C. Joyce ◽  
Vasanthe Vithanage ◽  
Alan H. Wearing
Keyword(s):  
Cell Walls ◽  
Floral Development ◽  
Middle Lamella ◽  
Floral Organ ◽  
Abscission Zone ◽  
Adjacent Cell ◽  
Flower Buds ◽  
Floral Tube ◽  
Exogenous Ethylene ◽  
Chamelaucium Uncinatum

Postharvest abscission of Geraldton waxflower (Chamelaucium uncinatum Schauer) flower buds and flowers is ethylene-mediated. Exposure of floral organs to exogenous ethylene (1 µL L–1) for 6 h at 20°C induced separation at a morphologically and anatomically distinct abscission zone between the pedicel and floral tube. Flower buds with opening petals and flowers with a nectiferous hypanthium were generally more responsive to exogenous ethylene than were flower buds enclosed in shiny bracteoles and aged (senescing) flowers. The anatomy of abscission-zone cells did not change at sequential stages of floral development from immature buds to aged flowers. The zone comprised a layer of small, laterally elongated-to-rounded, closely packed and highly protoplasmic parenchyma cells. Abscission occurred at a two- to four-cell-wide separation layer within the abscission zone. The process involved degradation of the middle lamella between separation layer cells. Following abscission, cells on both the proximal and distal faces of the separation layer became spherical, loosely packed and contained degenerating protoplasm. Central vascular tissues within the surrounding band of separation layer cells became torn and fractured. For flower buds, bracteoles that enclose the immature floral tube also separated at an abscission zone. However, this secondary abscission zone appeared less sensitive to ethylene than the primary (central) floral-tube abscission zone as bracteoles generally only completely abscised when exposed to 10 µL L–1 ethylene for the longer period of 24 h at 20°C. The smooth surfaces of abscised separation-layer cells suggest that hydrolase enzymes degrade the middle lamella between adjacent cell walls.

The morphology of grain abscission in Zizania aquatica

1980 ◽  
Vol 58 (21) ◽  
pp. 2269-2273 ◽  
Author(s):  
H. B. Hanten ◽  
G. E. Ahlgren ◽  
J. B. Carlson
Keyword(s):  
Wild Rice ◽  
Cell Walls ◽  
Vascular Tissue ◽  
Embryo Sac ◽  
Middle Lamella ◽  
Abscission Zone ◽  
Rice Grains ◽  
Zizania Aquatica ◽  
Parenchyma Cells ◽  
Anatomical Evidence

The anatomical development of the abscission zone in grains of Zizania aquatica L. was correlated with development of the embryo. The abscission zone is well developed when the embryo sac is mature. Soon after pollination, the first anatomical evidence of abscission appears as plasmolysis of the separation layer parenchyma cells. This is followed by separation of the layers by dissolution of the middle lamella and fragmentation of cell walls. Persistence of intact vascular tissue and presence of a surrounding cone-shaped mass of lignified cells may be involved in abscission of wild rice grains.

scholarly journals Control of Organ Abscission and Other Cell Separation Processes by Evolutionary Conserved Peptide Signaling

Plants ◽  
2019 ◽  
Vol 8 (7) ◽  
pp. 225 ◽  
Author(s):  
Chun-Lin Shi ◽  
Renate Marie Alling ◽  
Marta Hammerstad ◽  
Reidunn B. Aalen
Keyword(s):  
Cell Separation ◽  
Plant Hormone ◽  
Middle Lamella ◽  
Floral Organ ◽  
Adjacent Cell ◽  
Promoting Effect ◽  
Separation Processes ◽  
Severe Problem ◽  
Number Of Genes ◽  
Genes Encoding

Plants both generate and shed organs throughout their lifetime. Cell separation is in function during opening of anthers to release pollen; floral organs are detached after pollination when they have served their purpose; unfertilized flowers are shed; fruits and seeds are abscised from the mother plant to secure the propagation of new generations. Organ abscission takes place in specialized abscission zone (AZ) cells where the middle lamella between adjacent cell files is broken down. The plant hormone ethylene has a well-documented promoting effect on abscission, but mutation in ethylene receptor genes in Arabidopsis thaliana only delays the abscission process. Microarray and RNA sequencing have identified a large number of genes differentially expressed in the AZs, especially genes encoding enzymes involved in cell wall remodelling and disassembly. Mutations in such genes rarely give a phenotype, most likely due to functional redundancy. In contrast, mutation in the INFLORESCENCE DEFICIENT IN ABSCISSION (IDA) blocks floral organ abscission in Arabidopsis. IDA encodes a small peptide that signals through the leucine-rich repeat receptor-like kinases HAESA (HAE) and HAE-LIKE2 (HSL2) to control floral organ abscission and facilitate lateral root emergence. Untimely abscission is a severe problem in many crops, and in a more applied perspective, it is of interest to investigate whether IDA-HAE/HSL2 is involved in other cell separation processes and other species. Genes encoding IDA and HSL2 orthologues have been identified in all orders of flowering plants. Angiosperms have had enormous success, with species adapted to all kinds of environments, adaptations which include variation with respect to which organs they shed. Here we review, from an evolutionary perspective, the properties of the IDA-HAE/HSL2 signaling module and the evidence for its hypothesized involvement in various cell separation processes in angiosperms.

Silicification of wood-cell walls

1994 ◽  
Vol 52 ◽  
pp. 428-429
Author(s):  
S. E. Keckler ◽  
D. M. Dabbs ◽  
N. Yao ◽  
I. A. Aksay
Keyword(s):  
Electron Microscopy ◽  
Cell Wall ◽  
Cell Walls ◽  
Lignin Content ◽  
Resin Composite ◽  
Middle Lamella ◽  
Cellulose Fibers ◽  
Complex Structures ◽  
Rich Region ◽  
Inorganic Precursors

Cellular organic structures such as wood can be used as scaffolds for the synthesis of complex structures of organic/ceramic nanocomposites. The wood cell is a fiber-reinforced resin composite of cellulose fibers in a lignin matrix. A single cell wall, containing several layers of different fiber orientations and lignin content, is separated from its neighboring wall by the middle lamella, a lignin-rich region. In order to achieve total mineralization, deposition on and in the cell wall must be achieved. Geological fossilization of wood occurs as permineralization (filling the void spaces with mineral) and petrifaction (mineralizing the cell wall as the organic component decays) through infiltration of wood with inorganics after growth. Conversely, living plants can incorporate inorganics into their cells and in some cases into the cell walls during growth. In a recent study, we mimicked geological fossilization by infiltrating inorganic precursors into wood cells in order to enhance the properties of wood. In the current work, we use electron microscopy to examine the structure of silica formed in the cell walls after infiltration of tetraethoxysilane (TEOS).

scholarly journals Ethylene and 1-methylcyclopropene action over senescence of nasturtium flowers

2015 ◽  
Vol 33 (4) ◽  
pp. 453-458 ◽  
Author(s):  
Tania P Silva ◽  
Fernando L Finger
Keyword(s):  
Floral Development ◽  
Development Stage ◽  
Flower Senescence ◽  
Premature Senescence ◽  
Flower Opening ◽  
Development Stages ◽  
Post Harvest ◽  
The Third ◽  
Exogenous Ethylene ◽  
Floral Bud

ABSTRACT: This work describes ethylene and 1-methylcyclopropene (1-MCP) action on post-harvest shelf life of four development stages of nasturtium flowers. To reach this goal, we carried out three experiments. In the first and second experiments, we studied five ethylene (0; 0.1; 1; 10; 100 and 1000 μL/L) and three 1-MCP concentrations (0.25; 0.5 and 0.75 μL/L), respectively. In the third experiment, 1-MCP was followed by combined with ethylene (only 1-MCP; only ethylene; and 24 hours of exposure to 0.75 μL/L 1-MCP followed by 24 hours of exposure to 100 μL/L ethylene). All experiments had two control treatments, one keeping non-exposed flowers inside and another outside exposure chambers. Experiments were set in factorial design, in complete blocks at random, with four 10-flower replications each. Flower senescence was determined by a pre-established visual scale and by observing floral bud development. Ethylene dose above 10 μL/L induced flower wilting and premature senescence from the second floral development stage. Furthermore, higher concentrations of exogenous ethylene promoted irregular flower opening and/or morphological abnormalities in opened flowers. 1-MCP effectively extended post-harvest longevity of nasturtium flowers, independent of the concentration and even in the presence of exogenous ethylene.

UV-microscopic analysis of acetylated spruce and birch cell walls

Holzforschung ◽  
2004 ◽  
Vol 58 (5) ◽  
pp. 483-488 ◽  
Author(s):  
Christian Hansmann ◽  
Manfred Schwanninger ◽  
Barbara Stefke ◽  
Barbara Hinterstoisser ◽  
Wolfgang Gindl
Keyword(s):  
Cell Walls ◽  
Middle Lamella ◽  
Microscopic Analysis ◽  
Weight Percent ◽  
Cellular Level ◽  
Uv Spectrum ◽  
Spectral Shifts ◽  
Microscopy Analysis ◽  
Absorbance Peak ◽  
Absorbance Spectra

Abstract Spruce and birch earlywood was acetylated to different weight percent gains using three different acetylation procedures. The absorbance spectra of secondary cell wall and compound cell corner middle lamella were determined by means of UV microscopy. Analysis of the spectra showed that the characteristic lignin absorbance peak in the UV spectrum of wood around 280 nm shifted to shorter wavelengths in acetylated samples. A distinct relationship between achieved weight percent gains after acetylation and observed spectral shifts could be established revealing a certain potential to measure acetylation on a cellular level by means of UV microscopy.

The preprophase band: possible involvement in the formation of the cell wall

1976 ◽  
Vol 22 (2) ◽  
pp. 403-411 ◽  
Author(s):  
M.J. Packard ◽  
S.M. Stack
Keyword(s):  
Cell Wall ◽  
Allium Cepa ◽  
Cell Walls ◽  
Preprophase Band ◽  
Adjacent Cell ◽  
Root Tips ◽  
Meristematic Cells ◽  
Narrow Region ◽  
The Matrix

Numerous vesicles were observed among the microtubules of the “preprophase” band in prophase cells from root tips of Allium cepa. The content of these vesicles looks similar to the matrix of adjacent cell walls, and these vesicles often appear to be involved in exocytosis. In addition, the cell walls perpendicular to the plane of (beneath) the preprophase band are often differentially thickened compared to the walls lying parallel to the plane of the band. Our interpretation of these observations is that the preprophase band may direct or channel vesicles containing precursors of the cell wall to localized regions of wall synthesis. The incorporation of constituents of the cell wall into a narrow region defined by the position of the preprophase band may be a mechanism that ensures unidirecitonal growth of meristematic cells.

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.

scholarly journals RcAP1, a Homolog of APETALA1, is Associated with Flower Bud Differentiation and Floral Organ Morphogenesis in Rosa chinensis

2019 ◽  
Vol 20 (14) ◽  
pp. 3557 ◽  
Author(s):  
Yu Han ◽  
Aoying Tang ◽  
Jiayao Yu ◽  
Tangren Cheng ◽  
Jia Wang ◽  
...  
Keyword(s):  
Floral Organ ◽  
Flower Buds ◽  
Flower Bud ◽  
Floral Organs ◽  
Rosa Chinensis ◽  
Organ Morphogenesis ◽  
Floral Primordia ◽  
Flower Bud Differentiation ◽  
Delayed Flowering

Rosa chinensis is one of the most popular flower plants worldwide. The recurrent flowering trait greatly enhances the ornamental value of roses, and is the result of the constant formation of new flower buds. Flower bud differentiation has always been a major topic of interest among researchers. The APETALA1 (AP1) MADS-box (Mcm1, Agamous, Deficiens and SRF) transcription factor-encoding gene is important for the formation of the floral meristem and floral organs. However, research on the rose AP1 gene has been limited. Thus, we isolated AP1 from Rosa chinensis ‘Old Blush’. An expression analysis revealed that RcAP1 was not expressed before the floral primordia formation stage in flower buds. The overexpression of RcAP1 in Arabidopsis thaliana resulted in an early-flowering phenotype. Additionally, the virus-induced down-regulation of RcAP1 expression delayed flowering in ‘Old Blush’. Moreover, RcAP1 was specifically expressed in the sepals of floral organs, while its expression was down-regulated in abnormal sepals and leaf-like organs. These observations suggest that RcAP1 may contribute to rose bud differentiation as well as floral organ morphogenesis, especially the sepals. These results may help for further characterization of the regulatory mechanisms of the recurrent flowering trait in rose.

Ultrastructural Changes in the Cell Walls of Cambial Derivatives During Wood Formation in Indian ELM (Holoptelea Integrifolia)

IAWA Journal ◽  
2012 ◽  
Vol 33 (4) ◽  
pp. 403-416 ◽  
Author(s):  
Karumanchi S. Rao ◽  
Yoon Soo Kim ◽  
Pramod Sivan
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Middle Lamella ◽  
Ultrastructural Changes ◽  
Cell Wall Polysaccharides ◽  
Lignin Distribution ◽  
Parenchyma Cells ◽  
Ray Cells ◽  
Xylem Elements ◽  
S2 Layer

Sequential changes occurring in cell walls during expansion, secondary wall (SW) deposition and lignification have been studied in the differentiating xylem elements of Holoptelea integrifolia using transmission electron microscopy. The PATAg staining revealed that loosening of the cell wall starts at the cell corner middle lamella (CCML) and spreads to radial and tangential walls in the zone of cell expansion (EZ). Lignification started at the CCML region between vessels and associated parenchyma during the final stages of S2 layer formation. The S2 layer in the vessel appeared as two sublayers,an inner one and outer one.The contact ray cells showed SW deposition soon after axial paratracheal parenchyma had completed it, whereas noncontact ray cells underwent SW deposition and lignification following apotracheal parenchyma cells. The paratracheal and apotracheal parenchyma cells differed noticeably in terms of proportion of SW layers and lignin distribution pattern. Fibres were found to be the last xylem elements to complete SW deposition and lignification with differential polymerization of cell wall polysaccharides. It appears that the SW deposition started much earlier in the middle region of the fibres while their tips were still undergoing elongation. In homogeneous lignin distribution was noticed in the CCML region of fibres.

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