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Chalaza end had characteristic hypostase structure .
合点端有明显的承珠盘结构。
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After the newborn endosperm nuclei divided , the cells were formed step by step from the chalaza side to the micropyle side .
次生极核于合点端受精后,逐渐分裂形成细胞。
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The research mainly includes the development processes of embryo and endosperm , pericarp and spermoderm as well as the changes of nucellus and chalaza .
主要包括胚与胚乳的发育过程,果皮与种皮的发育,珠心与合点的变化。
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The megasporocyte forms in late March and undergoes meiosis to form the megaspore tetrad in early April , The functional megaspore lies nearby the chalaza end .
3月下旬大孢子母细胞形成,4月初进行减数分裂形成四分体,功能大孢子位于近合点端。
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With the embryo development , most of the endosperm degenerated , and the cells near chalaza entered the chalaza , digested it and further nourished the embryo .
合点端的胚乳细胞则侵入合点珠心组织,为胚进一步发育提供营养。
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However , the nucellus cells at the chalaza end split and reproduce , which results in the appearance of an expanded apophysis that keeps its shape until the seed becomes mature during the development process of the fruit in the coming year .
而合点端的珠心细胞不断分裂增值,在来年的果实发育过程中,形成一球状的膨大突起并保持到种子成熟。
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The megaspore mather cell is derived from the sporogenous cell , and divided into four megaspores by the meiotic division , megaspores present the rank of T & type , among which only one near chalaza can be developed to the embryo sac .
造孢细胞直接发育成大孢子母细胞,它进行减数分裂形成四个呈T&形排列的大孢子,只有合点端的一个大孢子发育成胚囊。
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Then the one cell near Chalaza end , which was derived from basal cell , underwent perpendicular division again , together with cells derived from apical cell , they formed embryo proper , and then sequentially formed multicellular spherical proembryo , heart-shaped embryo , Torpedo-shaped embryo , mature embryo .
由基细胞分裂来的近合点端的一个细胞再发生纵裂,和从顶细胞分裂来的细胞共同参与胚体的形成,进而产生多细胞球形原胚,心形胚,鱼雷形胚,成熟胚。