Development of endodermal Casparian bands and xylem in lateral roots of broad bean

1990 ◽  
Vol 68 (12) ◽  
pp. 2729-2735 ◽  
Author(s):  
Carol A. Peterson ◽  
Barbara E. M. Lefcourt
Keyword(s):  
Broad Bean ◽  
Lateral Roots ◽  
Staining Procedure ◽  
Tracheary Elements ◽  
Main Root ◽  
Fluorochrome Staining ◽  
Primary Xylem ◽  
Casparian Bands ◽  
Casparian Band

A clearing and fluorochrome staining procedure for broad bean (Vicia faba L. cv. Windsor) roots with laterals was devised which allowed observation of their tracheary elements and Casparian bands in situ. The Casparian band of the main root overlying the primordium disappeared early in its development and the margins of the remaining band were displaced outward during subsequent growth of the lateral. The Casparian band matured centripetally in parenchyma across the base of the lateral as far as the endodermis of the lateral and then acropetally into the lateral itself. Casparian bands of the laterals were always connected to those of the main roots. In actively growing roots, the primordium may have emerged as far as 2.7 mm from the main root and still contain no differentiating xylem or Casparian band. Longer laterals contained differentiating xylem 3 mm from the tip and maturing Casparian bands 5 mm from the tip. In nongrowing roots, some primordia not yet emerged from the main root had mature xylem tracheary elements 0.4 mm from the tip and mature Casparian bands 0.25 mm from the tip. Key words: Casparian band, primary xylem, lateral roots, endodermis.

Suberin deposition and band plasmolysis in the corn (Zea mays L.) root exodermis

1997 ◽  
Vol 75 (7) ◽  
pp. 1188-1199 ◽  
Author(s):  
Daryl E. Enstone ◽  
Carol A. Peterson
Keyword(s):  
Zea Mays ◽  
Zea Mays L ◽  
Lateral Roots ◽  
Root Surface ◽  
Casparian Bands ◽  
Suberin Lamellae ◽  
Tight Connection ◽  
Casparian Band ◽  
Apoplastic Barrier ◽  
Suberin Lamella

The exodermal Casparian band in corn (Zea mays L.) was first seen 10 mm distal to the kernel 4 days after planting. From its inception, the band usually occupied most of the radial wall (as seen in a cross section of the root). Subsequent maturation of the band around the root was asynchronous into the region of emerging lateral roots. Thus, a continuous apoplastic barrier would have been absent over much of the young root surface. Suberin lamellae development was also asynchronous, as these structures formed in those cells which had Casparian bands. Frequently, a lamella was initially deposited in patches, progressing centripetally until a continuous lipid layer was formed around the cell protoplast. Many instances of band plasmolysis (typical of the endodermis) were observed in the developing uniform exodermis. It could occur in cells with no detectable Casparian bands, suggesting that the tight connection between the plasmalemma and the wall that causes this phenomenon is not due to hydrophobic attractions. The results are consistent with the idea that there are strong attractions between proteins of the membrane and wall in the region of the Casparian band. The tight connection between the plasmalemma and the wall was broken during the later stages of suberin lamella development. Key words: Zea mays L., Poaceae, band plasmolysis, exodermis, Casparian band, suberin lamella.

scholarly journals Structure of Panax quinquefolius L. (Araliaceae) Roots with Emphasis on Secretory Duct Formation

1998 ◽  
Vol 123 (5) ◽  
pp. 798-801 ◽  
Author(s):  
R. Larry Peterson ◽  
Gregory T. Varney ◽  
Shannon Binns
Keyword(s):  
Lateral Roots ◽  
Primary Root ◽  
Secondary Growth ◽  
Panax Quinquefolius ◽  
Secondary Phloem ◽  
Primary Xylem ◽  
Casparian Bands ◽  
Transmission Electron ◽  
Anatomical Localization ◽  
Secretory Ducts

Primary and first-order lateral roots of Panax quinquefolius L. (American ginseng) were collected from plants in an experimental garden during their second year of growth and processed for light and transmission electron microscopy. Roots in primary growth had either a diarch or triarch primary xylem pattern, a pericycle, an endodermis with Casparian bands and subsequently a suberized cell wall, and a cortex of variable thickness with a suberized hypodermal layer. Both root types underwent rapid secondary growth and the primary root particularly formed a fleshy storage organ. The secondary phloem and secondary xylem had abundant parenchyma and few conducting elements. Secretory ducts differentiated in tissue derived from the pericycle and in the secondary phloem. Each schizogenous duct consisted of six to eight epithelial cells, which possessed dense, globular deposits but lacked starch. A phellogen, which produced several layers of suberized phellem, was initiated in the periphery of tissue derived from the pericycle. The results of this study clarify the anatomical localization of secretory duets in roots of this species.

Development of Common Milkweed (Asclepias syriaca) Root Buds Following Emergence from Lateral Roots

Weed Science ◽  
1988 ◽  
Vol 36 (6) ◽  
pp. 758-763 ◽  
Author(s):  
Elizabeth J. Stamm-Katovich ◽  
Donald L. Wyse ◽  
David D. Biesboer
Keyword(s):  
Vascular System ◽  
Lateral Roots ◽  
Vascular Bundles ◽  
Tracheary Elements ◽  
Asclepias Syriaca ◽  
Primary Xylem ◽  
Root Segments ◽  
Common Milkweed Asclepias Syriaca ◽  
Anatomical Constraints ◽  
Root Buds

In common milkweed, the development of subterranean root buds on excised root segments, following emergence from the parent root, is characterized by development of nodes and internodes followed by internode expansion. Transverse sections of root buds reveal that bicollateral vascular bundles as well as leaf traces and gaps are well developed in buds from 3-month-old plants. Strands of xylem and phloem connect the parent root and root bud in both inhibited and noninhibited root buds. Pitted primary tracheary elements, characteristic of developmentally advanced primary xylem, are present in these traces. The occurrence of a well-developed vascular system throughout the root bud and between the parent root and bud provides evidence that retardation of growth of inhibited root buds in common milkweed is not caused by anatomical constraints.

A rapid fluorescence technique to probe the permeability of the root apoplast

1992 ◽  
Vol 70 (7) ◽  
pp. 1493-1501 ◽  
Author(s):  
Daryl E. Enstone ◽  
Carol A. Peterson
Keyword(s):  
Plant Tissue ◽  
Broad Bean ◽  
Potassium Thiocyanate ◽  
Toxicity Tests ◽  
Fluorescence Technique ◽  
Tracheary Elements ◽  
Bright Yellow ◽  
Primary Roots ◽  
Casparian Band ◽  
Apoplastic Tracer

The alkaloid berberine is useful as a mobile apoplastic tracer. It is readily precipitated by thiocyanate, forming bright yellow, needle-like, fluorescent crystals. When berberine hemisulphate and potassium thiocyanate are applied sequentially to plant tissue, the crystals form in unmodified walls and in the lumina of dead cells such as tracheary elements. Lignified and suberized walls stain with berberine but do not develop crystals. Regions of the plant that have been penetrated by the chemicals can be located by preparing freehand sections, mounting them in potassium thiocyanate to inhibit dissolution of the crystals, and examining them with a fluorescence microscope. When the two chemicals are sequentially introduced into the xylem of onion, corn, and broad bean roots, the tracer does not pass the endodermal Casparian band, indicating that the system traces apoplastic pathways. The chemical concentrations that produce sufficient crystals so that berberine can be used as an apoplastic tracer in primary roots are 0.05% berberine hemisulphate and 0.09 M potasium thiocyanate. These concentrations were not toxic to cells of onion bulb epidermis. They reduced the growth rates of corn and broad bean roots but did not kill them. Berberine–thiocyanate is a useful apoplastic tracer provided care is taken not to exceed the limits of berberine toxicity to the tissue. Key words: apoplastic tracer, berberine hemisulphate, potassium thiocyanate, roots, toxicity tests, corn, onion, broad bean.

scholarly journals Three-dimensional in situ morphometrics of Mycobacterium tuberculosis infection within lesions by optical mesoscopy and novel acid-fast staining

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Robert J. Francis ◽  
Gillian Robb ◽  
Lee McCann ◽  
Bhagwati Khatri ◽  
James Keeble ◽  
...  
Keyword(s):  
Mycobacterium Tuberculosis ◽  
Three Dimensional ◽  
Large Field ◽  
Staining Procedure ◽  
3D Analysis ◽  
Mycobacterium Tuberculosis Infection ◽  
In Vivo Models ◽  
Novel Approach

AbstractTuberculosis (TB) preclinical testing relies on in vivo models including the mouse aerosol challenge model. The only method of determining colony morphometrics of TB infection in a tissue in situ is two-dimensional (2D) histopathology. 2D measurements consider heterogeneity within a single observable section but not above and below, which could contain critical information. Here we describe a novel approach, using optical clearing and a novel staining procedure with confocal microscopy and mesoscopy, for three-dimensional (3D) measurement of TB infection within lesions at sub-cellular resolution over a large field of view. We show TB morphometrics can be determined within lesion pathology, and differences in infection with different strains of Mycobacterium tuberculosis. Mesoscopy combined with the novel CUBIC Acid-Fast (CAF) staining procedure enables a quantitative approach to measure TB infection and allows 3D analysis of infection, providing a framework which could be used in the analysis of TB infection in situ.

Comparative Karyotype Investigations in the European Crayfish Astacus astacus and A. leptodactylus (Decapoda, Astacidae)

Crustaceana ◽  
2011 ◽  
Vol 84 (12-13) ◽  
pp. 1497-1510 ◽  
Author(s):  
M. Pavlica ◽  
M. Mcžić ◽  
G. Klobučar ◽  
M. Šrut ◽  
I. Maguire ◽  
...  
Keyword(s):  
Chromosome Number ◽  
Chromosome Complement ◽  
Size Difference ◽  
45S Rdna ◽  
Astacus Astacus ◽  
Fluorochrome Staining ◽  
Rdna Sites ◽  
Freshwater Habitats ◽  
Acrocentric Chromosomes

AbstractThis study reports on the chromosome number and karyological characteristics of the endangered species of European crayfish, Astacus astacus and A. leptodactylus (Decapoda, Astacidae), both native to Croatian freshwater habitats. The karyotype of A. astacus and A. leptodactylus consists of 2n = 176 and 2n = 180 chromosomes, respectively. The haploid chromosome complement of A. astacus consists of 52 metacentric, 35 metacentric-submetacentric, and 1 acrocentric chromosomes. Fluorochrome staining with 4,6-diamino-2-phenylindole (DAPI) has revealed that the karyotypes of A. astacus and A. leptodactylus are characterized by large heterochromatic blocks located at centromeric and intercalary positions on the chromosomes. Interstitial heterochromatic blocks were more frequent in A. astacus than in A. leptodactylus. In both species pairing of chromosomes in meiosis was regular with the majority of bivalents in a ring- and a dumbbell-form. Fluorescence in situ hybridization (FISH) has revealed that two 45S rDNA loci were present in the investigated species. In A. astacus one of the two 45S rDNA-bearing chromosome pairs was highly heteromorphic, exhibiting a three-fold size difference between 45S rDNA sites on homologous chromosomes. Such a size difference was significantly less pronounced in A. leptodactylus. The karyotype differences between A. astacus and A. leptodactylus suggest changes in chromosome number as well as position of repetitive DNAs have played a role in the karyotype evolution of the species of Astacus.

scholarly journals Comparative molecular cytogenetics in Melipona Illiger species (Hymenoptera, Apidae)

Sociobiology ◽  
2018 ◽  
Vol 65 (4) ◽  
pp. 696 ◽  
Author(s):  
Vanderly Andrade-Souza ◽  
Olivia Maria Pereira Duarte ◽  
Cinthia Caroline Cardoso Martins ◽  
Igor Silva Santos ◽  
Márcio Gilberto Cardoso Costa ◽  
...  
Keyword(s):  
In Situ Hybridization ◽  
Chromosome Number ◽  
Fluorescent In Situ Hybridization ◽  
Molecular Cytogenetics ◽  
Fluorochrome Staining ◽  
Rdna Sites ◽  
Cytogenetic Studies ◽  
Melipona Species ◽  
Almost All

Cytogenetic studies in Melipona are scarce with only 24 species analyzed cytogenetically. Of these, six species had the rDNA sites physically mapped and characterized by Fluorescent in situ Hybridization (fish). The aim of this study was to perform karyotype analyzes on Melipona species from different regions of Brazil, with a greater sampling representative of the Amazonian fauna and using conventional, fluorochrome staining and FISH with heterologous rDNA probes. The predominant chromosome number was 2n = 18, however, the subspecies M. seminigra abunensis and M. s. pernigra showed 2n = 22 chromosomes. The karyotypes were symmetrical, however M. bicolor, M. quadrifasciata, M. flavolineata, M. fuscopilosa, M. nebulosa presented the first pair heteromorphic in length. CMA3+ blocks also exhibited heteromorphism of size and in almost all cases coincided with rDNA sites, except for M. crinita and M. nebulosa, which presented additional non-coincident CMA3+ blocks. The CMA/ rDNA sites were terminal and interstitial in species with high heterochromatic content, and pericentromeric in those species with low heterochromatic content. In addition to pointing out cytogenetic features of cytotaxonomic importance, the reorganization of the genome in Melipona is discussed.

scholarly journals Influence of Root Morphology on Ecological Slope Protection

2020 ◽  
Vol 198 ◽  
pp. 04036
Author(s):  
JI Xiaolei ◽  
XU Lanlan ◽  
YANG Guoping
Keyword(s):  
Root Morphology ◽  
Lateral Root ◽  
Lateral Roots ◽  
Soil Mass ◽  
Soil Reinforcement ◽  
Main Root ◽  
Protection Effect ◽  
Included Angle ◽  
Theoretical Support ◽  
Object Based

Ecological slope protection is of great importance for preventing the water and soil loss on bare slopes, improving the ecological environment, and realizing the sustainable ecosystem development. The root-soil composite slope consisting of homogenous soil mass and oleander root system was taken as the study object. Based on the mechanics principle of soil reinforcement by roots in ecological slope protection, the influences of the lateral root quantity of plants and included angle between main root and lateral root on the slope protection were investigated via the finite element (FE) software ABAQUS. The simulation results show that the larger the quantity of lateral roots, the more obvious the displacement reduction of the soil mass on the slope surface will be. The slope protection effect varies with the root morphology, the included angle between main root and lateral root is an important factor influencing the slope protection effect of plants, and the slope protection effect at included angle of 30° is apparently superior to that at 90°. The research results can provide a theoretical support for the plant selection in the ecological slope protection.

Expression of a Bet v 1 homologue gene encoding a PR 10 protein in birch roots: induction by auxin and localization of the transcripts by in situ hybridization

2001 ◽  
Vol 28 (1) ◽  
pp. 57 ◽  
Author(s):  
Pascal Poupard ◽  
Nicole Brunel ◽  
Nathalie Leduc ◽  
Jean-Daniel Viémont ◽  
Désiré-Georges Strullu ◽  
...  
Keyword(s):  
In Situ Hybridization ◽  
Abiotic Factors ◽  
Lateral Roots ◽  
Northern Blotting ◽  
Root Tip ◽  
Gene Encoding ◽  
High Accumulation ◽  
Bet V 1 ◽  
Polymerase Chain

In birch roots (Betula pendula Roth), two members of the Bet v 1 gene family which encode PR 10 proteins have previously been characterized. One of these members, named Bet v 1-sc1, is significantly induced in response to biotic or abiotic factors. We have analysed the expression of Bet v 1-sc1 in birch roots treated either with 1 M indole-3-acetic acid (IAA) or 1 M kinetin using reverse transcription–polymerase chain reaction (RT–PCR), northern blotting and competitive PCR. High accumulation of the Bet v 1-sc1 transcripts was recorded only after auxin application, while kinetin had no effect. By in situ hybridization, we have investigated the localization of Bet v 1-sc1 mRNA in birch roots after induction of the gene by root treatment with 1 M IAA. Using root tip sections, we showed that Bet v 1-sc1 is significantly expressed in the apical meristem and the procambium. In sections taken in the zone producing lateral roots, the presence of Bet v 1-sc1 was found at sites of emerging secondary root primordia. This first report of localization of Bet v 1-sc1 expression suggests that this gene could be involved in the processes leading to lateral root initiation.

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