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首页> 外文期刊>Journal of Applied Botany >Reproductive biology of the olive (Olea europaea L.) cultivar 'nabali baladi'
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Reproductive biology of the olive (Olea europaea L.) cultivar 'nabali baladi'

机译:橄榄('Olea europaea L.)品种'nabali baladi'的生殖生物学

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摘要

'Nabali Baladi' is the most common olive cultivar in Jordan. The final fruit set is very low, Specially in orchards planted only with this cultivar. This problem is very common in olive cultivars. Thus, the investigations focused on the development and the morphology of the reproductive organs: pollen grain quality and quantity,pollen germination and pollen tube growth, fertilisation and fruit set. Another two olive cultivars "Grossa de Spagna' and "Rasie' were used for cross-pollination. One month before anthesis, the two tetrasporangiate anthers were developed. About three weeks before anthesis, the microspore mother cells were observed clearly. Through a week, they developed to the microspore tetrade stage. Finally, the fully developed pollen grains could be observed about five days before anthesis. The pollen grain number of the pollinizers was higher than in 'Nabali Baladi'. The normal pollen grains were more than 82% for the three cultivars in both year. The pollen viability was tested on an agar medium 0, 8%, containing 10% sucrose and 50 ppm citric acid. Immersion of the pollen grains in olive oil before spreading them on the medium improved this test significantly. The pistil consists of a superior ovary, short style, and wet papillate stigma. It was developed about six days before anthesis. A protuberance structure arised from the placenta of the ovary about four weeks before anthesis which developed to the anatropous ovule. Each carpel contained two ovules and only one ovule developed to the seed. The first embryo sac mother cell could be recognised in the middle of the ovule about two weeks before anthesis. The embryo sac with eight nuclei was completed about two days before anthesis. The pollen tubes grew intercellularly through the stigma and the transmitting tissue in the style. One pollen tube entered the ovary to fertilise one ovule through the micropyle. The stigmas with a high pollen grain number had also a high number of germinated pollen grains. The flowers which had less than ten germinated pollen grains on the stigma had lower percentage of fertilised ovaries. In most of self-pollinated flowers, all germinated pollen grains could not penetrate the transmitting tissue in the style, while in open and cross-pollination, most of the flowers had germinated pollen grains, and the tubes grew through the transmitting tissue in the style. In open- and cross-pollinatin, the pollen tubes started to enter the ovules two to three days before in self-pollination. In addition to that, the percentage of the fertilised ovules in open-and cross-pollination was about three times higher than in self-pollination. One week after anthesis, there was no difference in length between the fertilised and the non-fertilised ovules. Two weeks after anthesis, the ovule length doubled and the non-fertilised ovules degenerated. From the third week till the seventh week after anthesis, the ovule grew almost logarithmically. Eight weeks after anthesis till the mature stage, there was no further increase in the ovule size. The nuclear endosperm started to develop five days after anthesis. It became cellular 15 days after anthesis. The absorption of the nucellus tissue and the endosperm was very clear during the embryo development. The zygote was observed nine days after anthesis. Four and five weeks after anthesis, it developed to a long narrow suspensor. Six weeks after anthesis, the embryo reached the globular stage. One week later, it started to develop two cotyledons (heart-shaped) which developed quickly to the full length 12 weeks after anthesis. Finally, the embryo and the partly absorbed endosperm reached the final stage about 22 weeks after anthesis. The perfect flowers abscised in two ways: the non-fertilised perfect flowers abscised through the second week after anthesis, and part of the fertilised flowers abscised from two to six weeks after anthesis. After that, there was no significant fruit drop. The fruit set in open-and cr
机译:“ Nabali Baladi”是约旦最常见的橄榄品种。最终的坐果率非常低,特别是在仅使用该品种种植的果园中。这个问题在橄榄品种中非常普遍。因此,研究的重点是生殖器官的发育和形态:花粉粒的质量和数量,花粉的萌发和花粉管的生长,受精和坐果。另外两个橄榄品种“ Grossa de Spagna”和“ Rasie”用于异花授粉。开花前一个月,发育了两个四孢子花药。花前约三周,清楚地观察到小孢子母细胞。经过一周的时间,它们发展到小孢子四态阶段。最后,在开花前约五天就可以观察到完全发育的花粉粒。授粉媒介的花粉粒数高于“ Nabali Baladi”。两个品种的正常花粉粒均超过82%。在0、8%,含有10%蔗糖和50 ppm柠檬酸的琼脂培养基上测试花粉生存力。将花粉粒浸入橄榄油中,然后将它们撒在培养基上,可以显着改善该测试效果。雌蕊由上卵巢,短型和湿的乳头状柱头组成。它是在开花前六天开发的。在花期前约四周,子房的胎盘形成了一个突起结构,并发展为向异房卵。每个心皮包含两个胚珠,只有一个胚珠发育到种子。在开花前约两周,可以在胚珠中间识别出第一个胚囊母细胞。在开花前约两天完成具有八个核的胚囊。花粉管通过柱头和透射型组织在细胞间生长。一根花粉管进入子房,使一个子房的卵子受精。花粉粒数高的柱头也有大量发芽的花粉粒。在柱头上具有少于十个发芽花粉粒的花具有较低的受精卵巢百分比。在大多数自花授粉花中,所有发芽的花粉粒都不能穿透花柱状的花粉组织,而在开放和异花授粉中,大多数花都已经发芽了花粉粒,并且花粉管穿过花柱穿过花粉的组织。在开放花粉和交叉花粉中,花粉管在自花授粉前两到三天开始进入胚珠。除此之外,开放授粉和异花授粉中受精胚珠的百分比大约是自花授粉中的三倍。花后一星期,受精卵和未受精卵的长度没有差异。花后两周,胚珠长度加倍,未受精的胚珠退化。从开花后的第三周到第七周,胚珠几乎成对数增长。花后八周直到成熟阶段,胚珠大小没有进一步增加。花后五天,核胚乳开始发育。花后15天变为细胞。在胚胎发育过程中,细胞核组织和胚乳的吸收非常明显。花期9天后观察到合子。花后四到五周,它长成一个狭窄的悬吊器。花后六周,胚胎达到球形。一周后,它开始发育两个子叶(心形),在花期后十二周迅速发育至全长。最后,花期后约22周,胚胎和部分被吸收的胚乳达到了最终阶段。理想花的脱落有两种方式:在开花后的第二周内,无受精的理想花会脱落;在开花后的两到六周内,部分受精的花会脱落。此后,果实没有明显下降。水果放在开

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