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孢子的细胞

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Subsequently, the tapetum cell began to disorganize, and it kept the strongest Ca^2+ fluorescence intensity from microspore to pollen maturity until the tapetum was disappeared completely.

在花药壁组织内Ca^2+分布也呈现规律性的变化:造孢组织时期,花药壁组织Ca^2+荧光强度在不同壁层组织中分布均匀;小孢子母细胞时期,药壁中层细胞Ca^2+荧光最强,绒毡层细胞次之;单核小孢子时期,绒毡层细胞呈解体状态,Ca^2+荧光最强,并保持到二核花粉时期直至绒毡层完全消失,但此时花药纤维层发育形成,表现出较强的Ca^2+荧光。

In the late of April of the second year, male inflorescences unbound and pollinated. When female inflorescences accepted the pollen grains, ovary development was increased in early May. With the development of either of the two ovule, funiculus, integument and nucellus were differentiated. Embryo sac mother cell came into being and the meiosis begins. Then fuctional megaspore developed into matured embryo sac that contain eight nucleuses. In the end of May, double fertilization generated.

次年,4月下旬,雄花序解螺旋散粉,雌花序开花授粉;5月上旬,雌花序授粉后,迅速增长,子房膨大,两个胚珠分化出珠柄、珠被和珠心,珠心中产生孢原细胞;5月中下旬,大孢子母细胞形成并减数分裂,功能性大孢子形成成熟的八核胚囊;5月底,发生双受精。

Female gametogenesis in higher plants undergoes various developmental changes, including the de novo formation of germline cells, the differentiation of the megaspore mother cell, meiosis, megaspore selection, and the development of the embryosac.

高等植物雌配子体的形成涉及孢原细胞和大孢子母细胞的确立与分化、大孢子发生、功能大孢子以及胚囊的形成和发育等多种复杂调控过程。随着当代生物技术及功能基因组学的发展,近年对雌配子体发育的研究已从细胞学描述逐渐过渡到对基因和发育调控分子机理的探索。

Ovule development began in August, and rectangle megasporocyte began to occur in December, and linear tetrads of megaspores were formed in meiosis. In most occasions, only the chalazal megaspore was functional.

云南红豆杉胚珠从8月开始发生,大孢子母细胞12月开始发生,呈方形,减数分裂后形成4个"一"字形大孢子,在大多数情况下,只有靠合点端的大孢子发育为功能大孢子。

In the functional cell such as archesporial cell,megasporocyte,dyad,tetrad and youngmegaspore,among which the three cells close to micropyle end do not degeneratewholly,no clear starch grains were observed as well as in the embryo sacs from singlenucleate embryo sac to 8-nucleate one just forming.

淀粉粒变化有规律性,在孢原细胞、大孢子母细胞、二分体、四分体和早期的大孢子(即四分体中近珠孔端的3个细胞未完全退化)等功能性细胞中未观察到明显的淀粉粒。

Botany of or relating to the cells in a sporangium that give rise to spores.

属于孢子细胞,或与在孢子囊里提供孢子生长的细胞有关。

Sporulation involves an inner cell maturing into a spore and an outer cell nurturing the developing spore.

孢子的形成包括孢子内部细胞的成熟和外部细胞对形成中孢子的营养供给。

Ovule development began in August, and rectangle megasporocyte began to occur in December, and linear tetrads of megaspores were formed in meiosis. In most occasions, only the chalazal megaspore was functional.

云南红豆杉胚珠从8月开始发生,大孢子母细胞12月开始发生,呈方形,减数分裂后形成4个&一&字形大孢子,在大多数情况下,只有靠合点端的大孢子发育为功能大孢子。

The first split of microspore mother cell is observed after one week after beginning of temperature arised under high temperature but the split of secondary sporogenous cell doesn't be found. The split of secondary sporogenous cell is still found after one week but the first split of microspore mother cell is observed after 12d under low temperature. Formating speed of male gametophyte is affected by temperature.

在高温条件下,开始加温1周后即看到小孢子母细胞进行第一次分裂,未观察到次生造孢细胞的分裂;在低温条件下,1周后仍能看到次生造孢细胞的分裂,12d后才看到小孢子母细胞进行第一次分裂。

Paraffin slides observation found that the microspore of the RNMS line failed to vacuolate after its morphogenesis, disassembled and disappeared at last. After microspore morphogenesis, the breaking down of tapetum cells was delayed until microspore breading down.

石蜡切片细胞学观察,发现该隐性核不育能形成正常的四分体孢子,四分体释放出小孢子后,在单核花粉进入液泡化时小孢子的发育异常,不进行正常的液泡化,逐渐开始解体和消失;相应的绒毡层在小孢子形成后的降解延迟,绒毡层细胞的体积略有增大,在小孢子降解快结束时也很快解体。

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