Abstract

The micromorphology of the nectaries and of other elements of the flower was examined by scanning electron microscopy (SEM). The anatomy of the nectaries was determined using light microscopy (LM). The inflorescences of <i>A. platanoides</i> comprise flowers included in two categories: functionally male and female. Nectaries of similar structure are found in both types of these flowers. The nectary gland located on the surface of the receptacle belongs to interstaminal nectaries. It has the form of a fleshy ring situated between the petals and the pistil. The bases of the staminal filaments are located in the depressions of the nectary. The outer diameter of the nectary reaches ca. 5 mm, while the thickness of this gland's tissues is 400-700 μm. In the epidermis of the nectary gland, there are numerous, evenly distributed stomata through which nectar release occurs. The stomata function asynchronously. In some stomata, we could observe nectar drops flowing out and a layer of this secretion around the stomata. The secretory parenchyma of the nectary is composed of several layers of thick-walled cells, whereas the ends of the vascular bundles with xylem and phloem elements are situated in the subglandular parenchyma. Chloroplasts are found both in the epidermal cells and in the glandular parenchyma cells and photosynthesis can take place in them due to the nectary's good exposure to light. The presence of starch grains was found in the chloroplasts; they can be energy material for nectar production.

Highlights

  • Norway maple (Acer platanoides L.) blooms for the first time at the age of 20 (Maurizio and Grafl, 1969)

  • The stamens reached an average length of 5.0 mm, whereas the poorly developed pistil 1.0 mm (Fig. 1G)

  • The stamens were 2.0 mm long and the pistil reached a height of 5.5 mm (Fig. 1F)

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Summary

Introduction

Norway maple (Acer platanoides L.) blooms for the first time at the age of 20 (Maurizio and Grafl , 1969). The flowers of this species form corymbs which develop before or simultaneously with leaves (Kugler , 1970; Szweykowscy , 2003). The pistil is composed of a two-chambered winged ovary and a style with two-lobbed stigma (Maurizio and Grafl , 1969; Lipiński , 2010). The flowers of this species are divided into several categories differing in stamen length and pistil size. Renner et al (2007) report that monoecy with heterodichogamy belongs to sexual strategies in the flowering biology of this species

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