scholarly journals Gloss, Colour and Grip: Multifunctional Epidermal Cell Shapes in Bee- and Bird-Pollinated Flowers

PLoS ONE ◽  
2014 ◽  
Vol 9 (11) ◽  
pp. e112013 ◽  
Author(s):  
Sarah Papiorek ◽  
Robert R. Junker ◽  
Klaus Lunau
Keyword(s):  
2021 ◽  
Vol 12 ◽  
Author(s):  
Kotomi Kikukawa ◽  
Kazuki Yoshimura ◽  
Akira Watanabe ◽  
Takumi Higaki

During cotyledon growth, the pavement cells, which make up most of the epidermal layer, undergo dynamic morphological changes from simple to jigsaw puzzle-like shapes in most dicotyledonous plants. Morphological analysis of cell shapes generally involves the segmentation of cells from input images followed by the extraction of shape descriptors that can be used to assess cell shape. Traditionally, replica and fluorescent labeling methods have been used for time-lapse observation of cotyledon epidermal cell morphogenesis, but these methods require expensive microscopes and can be technically demanding. Here, we propose a silver-nano-ink coating method for time-lapse imaging and quantification of morphological changes in the epidermal cells of growing Arabidopsis thaliana cotyledons. To obtain high-resolution and wide-area cotyledon surface images, we placed the seedlings on a biaxial goniometer and adjusted the cotyledons, which were coated by dropping silver ink onto them, to be as horizontal to the focal plane as possible. The omnifocal images that had the most epidermal cell shapes in the observation area were taken at multiple points to cover the whole surface area of the cotyledon. The multi-point omnifocal images were automatically stitched, and the epidermal cells were automatically and accurately segmented by machine learning. Quantification of cell morphological features based on the segmented images demonstrated that the proposed method could quantitatively evaluate jigsaw puzzle-shaped cell growth and morphogenesis. The method was successfully applied to phenotyping of the bpp125 triple mutant, which has defective pavement cell morphogenesis. The proposed method will be useful for time-lapse non-destructive phenotyping of plant surface structures and is easier to use than the conversional methods that require fluorescent dye labeling or transformation with marker gene constructs and expensive microscopes such as the confocal laser microscope.


HortScience ◽  
2003 ◽  
Vol 38 (4) ◽  
pp. 573-577 ◽  
Author(s):  
Rasika G. Mudalige ◽  
Adelheid R. Kuehnle ◽  
Teresita D. Amore

Perianths of 34 Dendrobium Sw. species and hybrids were examined to elucidate the roles of pigment distribution and shape of upper epidermal cells in determining color intensity, perception, and visual texture. Color intensity was determined by the spatial localization of anthocyanin in tissue layers, i.e., in the epidermal, subepidermal, and mesophyll layers, as well as by distribution of pigmented cells within the tissue layer. Anthocyanins were confined to the epidermal layer or subepidermal layer in flowers with low color intensity, whereas they were also in several layers of mesophyll in more intensely colored flowers. Striped patterns on the perianth were due to the restriction of pigment to cells surrounding the vascular bundles. Color perception is influenced by the presence or absence of carotenoids, which when present, were distributed in all cell layers. Anthocyanins in combination with carotenoids resulted in a variety of flower colors ranging from red, maroon, bronze to brown, depending on the relative location of the two pigments. Four types of epidermal cell shapes were identified in Dendrobium flowers: flat, dome, elongated dome, and papillate. Epidermal cell shape and cell packing in the mesophyll affected the visual texture. Petals and sepals with flat cells and a tightly packed mesophyll had a glossy texture, whereas dome cells and loosely packed mesophyll contributed a velvety texture. The labella in the majority of flowers examined had a complex epidermis with more than one epidermal cell shape, predominantly papillate epidermal cells.


2018 ◽  
Vol 11 (1) ◽  
pp. 148-154
Author(s):  
H.M. Abba ◽  
A Abdullahi ◽  
U.A. Yuguda

Leaf epidermal microscopy of Ipomoea carnea Jacq was studied to investigate the structure of the stomata and epidermal features which may be used for delimitation of the specie. Fresh leaves of Ipomoea carnea were obtained from five different LGA,S (Gombe, Y/deba, Balanga, Funakaye and Dukku ) in Gombe State, Nigeria. The specimens were studied under light microscope to examine the Stomatal features, Epidermal cell shapes and Anticlinal cell-wall patterns. It had the presence of amphistomatic leaves; one type of Stomatal complex type namely Cyclocytic. Accession 1 had the highest Stomatal Density (40.00 ± 1.00mm2) with lowest Stomatal size (51.13±7.47µm) on the Abaxial leaf surfaces while Accession 2 possessed lowest Stomatal density (23.40±7.67mm2) with highest Stomatal Size (88.68±1.95mm2) on the Adaxial leaf surfaces. Curved anticlinal cell wall patterns with polygonal epidermal cell shapes were also observed. It was concluded that the presence of Cylocytic type of stomata, with large stomatal sizes greatly helped in the delimitation of the plant and could also be used for classification /identification of the plant and some of the features such as trichomes could also be used for adaptation purposes.Keywords: Epidermal, Stomata, Ipomoea carnea, Cyclocytic, Trichomes


2020 ◽  
Vol 12 (3) ◽  
pp. 637-645
Author(s):  
Sunday A. ADENIRAN ◽  
Akeem B. KADIRI ◽  
JAMES D. OLOWOKUDEJO

A qualitative micromorphological assessment of the seven species of Isolona occurring in Nigeria and the Cameroons was undertaken with the aid of light microscope. The stomatal cells are particularly useful, providing stable characters which can be reliably employed in distinguishing the species. Hypostomatic leaves and paracytic stomatal type are generic constant. Possession of only paracytic stomata is characteristic of I. dewevrei whereas other species may have in addition another type such as 1+2 laterocytic stomatal type found only in I. zenkeri and presence of brachyparacytic stomata which shows relatedness of I. campanulata, I. congolana, I. hexaloba, I. pleurocarpus and I. thonneri. The epidermal surfaces appeared glabrous but an indication of hairs is shown by the presence of a glandular trichome base only in I. hexaloba. The epidermal cell characters such as epidermal cell shapes and anticlinal wall patterns seem to intergrade and they are not as definite as the stomatal cells. However, a combination of these features will be helpful in defining the species better and their leaf fragments can be differentiated based on the various characters studied for effective utilization in herbal medicinal research.


Biologija ◽  
2017 ◽  
Vol 63 (2) ◽  
Author(s):  
Seyed Mehdi Talebi ◽  
Mitra Noori ◽  
Habibeh Afzali Naniz

Euphorbia is the largest genus of Euphorbiaceae widely distributed all over the world. The genus members grow naturally in different parts of Iran and nearly 96 species of Euphorbia have been listed in the country. Investigations show that the traits of foliar epidermis have taxonomic values. That is why the features of epidermal leaf anatomy of 18 Euphorbia taxa were studied in the present study. Plant samples were collected from Kerman Province, Iran, and identified using available references. Semi-permanent slides were prepared of adaxial and abaxial leaf epidermis. Then the slides were studied using light microscopy and some epidermal leaf anatomy characteristics stomata types, trichomes, the shape and type of epidermal cell, and their walls were examined. Photomicrographs were taken from each sample. Results showed that stomata type were stable among the species. Not only leaf epidermal cell shapes differed between the taxa, but also in some species they varied between the abaxial and adaxial surfaces. These conditions hold true for cell wall patterns. Some of the studied taxa had simple and uniseriate trichomes on the epidermal surfaces, in most of them trichomes were present on both leaf surfaces, while in one species trichomes were seen on the abaxial surface. Our findings confirmed that some of the anatomical traits, such as the absence or presence of trichomes, epidermal cell shape, and anticlinal cell wall patterns had taxonomic value and are useful in the identification of taxa.


Author(s):  
N.C. Lyon ◽  
W. C. Mueller

Schumacher and Halbsguth first demonstrated ectodesmata as pores or channels in the epidermal cell walls in haustoria of Cuscuta odorata L. by light microscopy in tissues fixed in a sublimate fixative (30% ethyl alcohol, 30 ml:glacial acetic acid, 10 ml: 65% nitric acid, 1 ml: 40% formaldehyde, 5 ml: oxalic acid, 2 g: mecuric chloride to saturation 2-3 g). Other workers have published electron micrographs of structures transversing the outer epidermal cell in thin sections of plant leaves that have been interpreted as ectodesmata. Such structures are evident following treatment with Hg++ or Ag+ salts and are only rarely observed by electron microscopy. If ectodesmata exist without such treatment, and are not artefacts, they would afford natural pathways of entry for applied foliar solutions and plant viruses.


Author(s):  
Etienne de Harven

Biological ultrastructures have been extensively studied with the scanning electron microscope (SEM) for the past 12 years mainly because this instrument offers accurate and reproducible high resolution images of cell shapes, provided the cells are dried in ways which will spare them the damage which would be caused by air drying. This can be achieved by several techniques among which the critical point drying technique of T. Anderson has been, by far, the most reproducibly successful. Many biologists, however, have been interpreting SEM micrographs in terms of an exclusive secondary electron imaging (SEI) process in which the resolution is primarily limited by the spot size of the primary incident beam. in fact, this is not the case since it appears that high resolution, even on uncoated samples, is probably compromised by the emission of secondary electrons of much more complex origin.When an incident primary electron beam interacts with the surface of most biological samples, a large percentage of the electrons penetrate below the surface of the exposed cells.


1991 ◽  
Vol 53 (1) ◽  
pp. 3-6
Author(s):  
SHIN'ICHI INOHARA
Keyword(s):  

Sign in / Sign up

Export Citation Format

Share Document