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麻类所麻类育种五十年 总被引:1,自引:1,他引:0
本文全面回顾了麻类研究所麻类育种工作五十年的历程,较为详尽地阐明了麻类育种工作开展的过程.五十年的麻类育种工作经历了资源的收集整理和评价、鉴定与利用,常规育种技术运用和现代高新技术的引入.基本形成了我国麻类育种技术和新品种选育及配套技术推广应用体系.先后收集和整理麻类资源近万余份.选育出新品种30余个,在生产上发挥了重要作用.其中红麻品种"7804"、苎麻品种"圆叶青"和"中苎1号"及黄麻品种"湘黄麻1号"等品种在生产上大面积推广利用,取得了社会经济效益近100亿元.选育了亚麻品种中亚麻1号,结束了我国南方没有自育亚麻品种的历史.现代的麻类育种向多元化育种目标发展,为麻类的不同用途选育出专用品种. 相似文献
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广西香稻育种现状及发展策略 总被引:1,自引:0,他引:1
对21世纪以来广西香稻品种的审定情况及广西自育香稻品种的产量、品质以及抗性等进行统计分析,探明了广西香稻的育种现状及存在问题,如广西通过审定的香稻品种中自育品种较少,且多为常规稻品种;自育香稻品种的优质达标率较低,主要原因是直链淀粉含量偏低;自育香稻品种株高适中,多为大粒型品种,后期育成品种产量有所提高,主要通过育成大穗型品种来实现;自育香稻品种稻瘟病抗性整体较差,白叶枯病前期抗性表现较好、后期出现退步等。今后应加强香稻品种的选育力度,特别是杂交香稻品种的选育力度;加快香稻品种鉴定技术的研究和利用,为香稻品种的审定提供技术支撑;加强中等偏低直链淀粉含量香稻品种的选育,以市场需求为导向,制定广西优质稻米相关地方标准,特别注重直链淀粉含量标准的调整;把提高稻瘟病抗性作为香稻品种选育过程中的重点工作内容等。 相似文献
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利用花粉管通道法导入外源DNA技术是我国学者周光宇先生创建的 ,是我国基因工程研究中的一个特色。目前 ,花粉管通道法已在许多作物上得到了成功的应用。棉花花器大 ,繁殖系数高 ,尤其适用于采用花粉管通道法进行外源 DNA导入。目前我国培育和审定的转基因抗虫棉品种大多是以利用该技术获得的转基因抗虫材料为基础 ,通过系统选育或杂交选育而成的。山东棉花研究中心于 1 999年利用花粉管通道法将高产、抗病的海岛棉品系海71 2 4、异缘四倍体野生种达尔文氏棉及其他野生种系的叶片 DNA分别导入到陆地棉栽培品种石远32 1、鲁 735中 ,2 0 0… 相似文献
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日本茶树遗传育种研究 总被引:5,自引:0,他引:5
本文介绍了日本茶树遗传育种研究的发展过程。日本茶树育种的发展,主要得益于海外茶树品种资源的引进和利用,茶树育种的目标,早期注重红茶品种选育,随后以绿茶品种选育为主,进入80年代后期,又侧重于多抗品种的培育,优良无性系茶树品种的推广,促进了茶叶产量的提高,同时加快了茶叶加工和茶园机械化的发展,提高了茶叶生产的效益。茶树品种音一化和遗传育种资源不足是日本茶树育种研究存在的主要问题,海外茶的品种资源的收 相似文献
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广东花生育种研究 总被引:4,自引:1,他引:4
广东花生育种工作起步于20世纪50年代中期开始进行的农家种的征集评选,系选种的选育及其后的推广应用.60年代初期开始进行农家种的杂交选育及推广应用,并开展了辐射技术与杂交技术相结合的方法进行新品种的选育,成为辐射与杂交相结合育种的典范;1970年以前花生育种工作的重点是抗青枯病育种,1970年以后花生育种工作的重点是抗旱锈病育种兼抗青枯病育种.70年代中期开始直接利用外来种质和抗性基因改良花生抗病(青枯病、锈病、叶斑病)性并取得成效;1981~1986年抗锈遗传研究对选育高产抗锈病花生品种起到理论指导作用;育种家以农家种狮头企为基础亲本材料,经过50年不断遗传改良,形成了一个较大的花生品种群体.广东花生选育种历史实质上是农家种狮头企及其后代的遗传改良历史.广东花生育种工作及其品种的推广应用促进了广东和全国花生生产及育种的发展. 相似文献
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通过3年马铃薯小薯整播与切块播种对比试验,发现小薯整播表现出抗旱保苗、长势旺盛、抗病性强、增产显著的四大优点,为进一步提高马铃薯产量提供了重要依据。 相似文献
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Charles R. Brown 《Potato Research》2011,54(4):287-300
Conventional potato breeding refers to development of new cultivars from sexual crosses followed by clonal propagation and
selection. Nearly all new varieties of potato still emerge from this process free from modern technologies of gene insertion.
Conventional breeding remains the most important force for introduction of new phenotypes underlain by new genes. However,
these come from already selected potato breeding lines or named varieties or from wild potatoes or more distant solanaceous
relatives that are amenable to somatic hybridization. Potato breeders are constantly searching for new germplasm, in part
because the potato as a crop still remains highly vulnerable to biotic and abiotic stresses. In addition, the widening of
the genetic base is seen as a means of increasing heterozygosity. Despite a highly conscious import of genetic variability,
commercial varieties often emerge from a relatively restricted genetic pool. This is due to the long list of traits that must
fall within narrow boundaries of performance. The potato must be able to navigate the conditions of modern agriculture, withstand
unusual weather events, and arrive at harvest with skin and flesh appealing to the market for which it is intended. A storage
period must also be endured during which appearance and suitability for processing or the consumer’s kitchen must be maintained.
A lapse in any of these phases usually signals that a new variety will exit commercial use as fast as it entered. The inconvenient
accompaniment of introducing exotic genetic variation is that the breeding products are often outside of the targeted market
niche. It is not surprising that many new varieties stem from crosses from older named varieties. Efforts to diversify are
in conflict with conformism leading to relatively high co-ancestry coefficients between advanced breeding lines. Conventional
breeding has advanced through the last hundred years the appearance, sugar status, Verticillium resistance, and yield of larger sized tubers in statistically robust ways. Potato arrived from the new world and very quickly
became the secret solution to famine for the poor by virtue of its productivity and nutrient content. Meanwhile, in modern
times, challenges to the consumption of potato come from a sedentary and carbohydrate over-satiated society. The genetic repository
of potato germplasm is so rich that a new era of potato varieties beneficial to health may be at hand. Conventional breeding
will certainly be a major part of this. 相似文献
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China is the world’s leading producer of potatoes, growing 22% of all potatoes. Production continues to rise, owing to increases
in both land devoted to potato production and yield per hectare. Most potato production occurs in the northern and southwest
regions of the country. The processing of coarse starch is the most important component of the potato processing industry
in China, but other processing industries, such as crisps and French fries, are expanding. Major production constraints include
inadequate germplasm resources for cultivar development, the lack of high quality seed potatoes, and limited access to equipment
for mechanized cultivation, planting, fertilizing, spraying, and harvesting. Additional weaknesses in storage and transportation
technologies must be addressed, as they are the major constraints for the healthy development of the potato industry. The
introduction and improvement of these technologies will ensure the sustainable development of the potato industry in China. 相似文献
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二倍体杂种优势马铃薯育种的展望 总被引:1,自引:0,他引:1
《中国马铃薯》2013,(2):96-99
马铃薯育种进程缓慢主要是由马铃薯四倍体遗传特性决定的。高度杂合的四倍体马铃薯中隐性基因表现频率低,使得很多有害的等位基因被隐藏在四倍体中,而有利等位基因很难重组到一个四倍体品种中,这是造成马铃薯杂交育种周期长的一个重要原因。马铃薯无性繁殖有利于保持原品种的优良性,生育期短;但储运成本高、容易退化。实生籽利用的优点是储运简便、基本不传播病虫害,且有利于知识产权保护。与四倍体实生种相比,二倍体F1育种可以通过不断自交将有害基因剔除掉,从而获得优良自交系用于F1实生籽生产。随着马铃薯研究的不断发展和马铃薯全基因组测序的基本完成,近几年二倍体F1实生籽育种成为了国际马铃薯研究的热点。然而,要实现二倍体实生籽生产,自交不亲和及其自交衰退是培育自交系的绊脚石。我们正在克隆自交不亲和抑制基因Sli,并且通过杂交将该基因整合到优良栽培品种中,为下一步培育出优良二倍体自交系奠定基础。同时我们也正在全基因组水平上挖掘马铃薯自交衰退相关基因区域,希望能进一步了解自交衰退的遗传机理,探索一条快速克服自交衰退的分子育种路径。这些工作将有助于建立马铃薯二倍体F1育种体系,带动马铃薯产业进入新的"绿色革命"。 相似文献
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Marker-assisted Breeding for Disease Resistance in Potato 总被引:1,自引:1,他引:0
A. Carrasco J. E. Chauvin B. Trognitz A. Pawlak O. Rubio-Covarruvias E. Zimnoch-Guzowska 《Potato Research》2009,52(3):245-248
Sub-project 5 of BIOEXPLOIT aims to design durable disease resistance through marker-assisted breeding by converting existing
markers for high-throughput application, developing and validating high-throughput marker technologies and pyramiding major
R genes and/or quantitative trait loci into elite material. Activities include (1) the fine mapping of the quantitative trait
locus PiXspg which accounts for a large proportion of the variation in late blight resistance, (2) converting SNP-based markers and an
AFLP marker to easy-to-use-markers, (3) testing of progenies with combined sources of late blight resistance for presence
of R genes and agronomic features, (4) backcrossing new sources of resistance to S. tuberosum and molecular screening of breeding materials with marker GP94 linked with gene Rpi-phu1 conferring late blight resistance, (5) evaluating potato clones with enhanced resistance against Phytophthora infestans under field conditions of Toluca (México), and (6) developing populations and marker-assisted breeding for disease resistance. 相似文献