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sbornik_s_2011.pdf

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XI. Workshop of Physical Chemists and Electrochemists´11 Brno<br />

2. EXPERIMENT<br />

Plant material (roots, stems, leaves) was collected in the botanical garden of<br />

University of Veterinary and Pharmaceutical University Brno. For the anatomical study,<br />

transversal, radial and tangential hand-made sections were used. For the visualization of<br />

lignified plant tissues, ethanolic (50 %, v/v) mixture of acid fuchsine and malachite green<br />

(both 1%, w/w; Sigma-Aldrich, USA) was used. Sections were stained for four minutes<br />

and after it washed with acidic ethanol (60 %, v/v, with 37% hydrochloric acid 0.1 %, v/v,<br />

Sigma-Aldrich, USA). At once, sections, which were not stained, were used for<br />

microscopic analysis using fluorescence microscope (Carl Zeiss Axioscop 40, Zeiss,<br />

Germany). In addition, sections were stained by aqueous solution of acridine orange (1 %,<br />

w/w, Sigma-Aldrich, USA) for detection of non-lignified and lignified structures.<br />

3. RESULTS AND DISCUSSION<br />

The object of this study was focused on vegetative organs of Rhus hirta (L.) Sudw.<br />

Roots were observed only in the secondary state because of very early formation of<br />

vascular cambium, which produces elements of secondary xylem and secondary phloem.<br />

Secondary xylem of roots is typical due to presence of high number of vessels of large<br />

diameter. Amount of libriform is low; in addition, secondary cell walls if libriform are<br />

very thin and almost without lignification. Secondary phloem consists of sieve tubemembers,<br />

which are arranged in tangential groups, radial parenchyma forms well visible<br />

rays. Axial parenchyma of secondary phloem are associated with sieve tube-members. In<br />

the older parts of secondary phloem, there are large schizogenous intercellular cavities.<br />

Secondary dermal tissue periderm consists of layers of phellem cells with suberinised cell<br />

walls and 1-2-layered cork cambium (phellogene). Phelloderm is reduced to only several<br />

cells, which undergo sclerification under formation of sclereids (see Fig. 3).<br />

Stems as well as roots very early undergo process of secondary thickening due to<br />

activity of vascular cambium and cork cambium. However, epidermis persists after<br />

formation of vascular cambium. Some epidermal cells are modified into trichomes.<br />

Glandular trichomes, which are associated with production of some secondary<br />

metabolites, are typically multicellular. Cortex consists of collenchymatous hypodermis,<br />

parenchymatous mesodermis and indistinct endodermis- starch sheath. Vascular bundles<br />

are arranged in one ring (eustele) and are typically collateral. Elements of protophloem<br />

undergo sclerification under formation of sclerenchyma on the periphery of vascular<br />

bundles. Metaphloem is connected with formation of large schizogenous secretory<br />

cavities, each vascular bundle contains one cavity. In comparison with roots, secondary<br />

xylem of stem contains less vessels and higher amount of libriform with distinct secondary<br />

cell walls. Axial parenchyma is associated with vessels, ray parenchyma forms<br />

heterocellular rays. Pith is parenchymatous, some cells undergo sclerification and form<br />

individual sclereids. In addition, pith contains schizogenous intercellular cavities with<br />

distinct epithelial cells (see Fig. 4).<br />

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