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Genetic diversity of red rice in Arkansas and the role of gene flow in red rice diversification.

机译:阿肯色州红米的遗传多样性及其基因流在红米多样化中的作用。

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摘要

Red rice (Oryza sativa L.) is a noxious weed in rice production systems throughout the world. In the southern United States red rice has been a challenging weed since the beginning of rice production in 1685. Because it is of the same genus and species as cultivated rice, red rice can not be controlled with herbicides in conventional rice fields. Red rice infestation can decrease cultivated rice yield up to 80%. Lately, red rice can be selectively controlled using the imazethapyr-resistant Clearfield(TM) (CL) rice technology. To manage red rice better, information is needed regarding: (1) yield losses due to different red rice biotypes; (2) the reciprocal outcrossing frequencies between cultivated rice and red rice biotypes; (3) impact of plant and environmental factors on outcrossing rate" and (5) the extent of genetic introgression into cultivated rice from red rice in the last century.;Field and greenhouse experiments were conducted to examine (1) the variability in maximum outcrossing rate between 12 red rice biotypes and 'CL161' rice during their peak flowering overlap in the field and (2) the genetic compatibility of red rice biotypes with CL161 rice. In field experiments, the maximum outcrossing rate between red rice biotypes and CL161 ranged from 0.03 to 0.25%. In manual crosses between red rice biotypes and CL rice, seed set, which indicates genetic compatibility, ranged from 49 to 94%. The majority of red rice biotypes had similar compatibility with CL161 rice.;Field experiments were conducted to determine the impact of planting date, CL cultivars and red rice biotypes on the outcrossing rate. To further understand rice and red rice effects on outcrossing rate, we also aimed to determine the relative contribution of flowering time of CL rice and red rice biotypes and air temperature and relative humidity on outcrossing rate. Lower outcrossing rates were observed in late plantings compared with earlier planting. In general, a higher outcrossing rate (1.26%) was observed between red rice biotypes and CLXL8 hybrid rice than with CL161 rice (0.21%). The outcrossing rate of red rice biotypes with CL161 ranged from 0 to 0.21% and that with CLXL8 hybrid rice from 0 to 1.26%. Among the plant and environmental factors, red rice type is the main factor that influences the outcrossing rate with CL 161 rice. On the other hand, with CLXL8, the minimum relative humidity during the flowering influences outcrossing rate the most.;Experiments were also conducted to determine the gene flow rate from red rice biotypes to cultivated rice and to evaluate the morphology, phenology, and fecundity of resulting outcrossing. The gene flow rate from weedy rice to cultivated rice ranged from 0.01 to 0.2% and differed by red rice biotype. F1 crosses between CL161 rice x red rice were 138 to 150 cm tall and flowered 1 to 5 d later than CL161 rice. Seeds of all crosses had red pericarp, were pubescent, shattered at maturity, and germinated >90%.;Field experiments were conducted to evaluate the emergence pattern of red rice biotypes at different planting dates and evaluate the effect of red rice biotype, CL rice cultivar, and planting date on cultivated rice yield loss. The emergence rate of red rice biotypes increased with later planting dates. In general, CL rice yield losses due to red rice biotypes increased in later planting dates, up to 49%. CL rice yield losses from different red rice biotypes ranged from 14 to 45% and 6 to 35% in CL161 and CLXL8 hybrid rice, respectively. Cultivated rice becomes less competitive with red rice in later plantings, resulting in higher yield losses.;The genetic diversity in red rice populations in Arkansas and introgression of genetic material in these red rice populations from cultivated rice in the last 100 yrs was investigated. One hundred thirty-seven red rice accessions from four ecological zones in Arkansas and 36 rice cultivars that have been grown in Arkansas in the past century were fingerprinted using 27 rice microsatellite markers. All rice cultivars grown in Arkansas formed a cluster separate from red rice accessions. Generally, red rice accessions were separated in 4 groups: awnless strawhull, blackhull, brownhull, and awned strawhull, and some accessions between red rice biotypes and rice cultivars. Awnless strawhull accessions were genetically distant from blackhull (GD = 0.55) and brownhull (GD = 0.60). Also blackhull and brownhull types are genetically distant (GD = 0.96) to each other than awnless strawhull types. The blackhull and strawhull red rice diversity is affected by their zone of origin. Twenty-five percent of red rice accessions in Arkansas had some genetic material introgression from cultivated rice in the last century.
机译:红米(Oryza sativa L.)是全世界稻米生产系统中的一种有害杂草。自1685年开始生产稻米以来,在美国南部,红米一直是具有挑战性的杂草。由于它与栽培稻具有相同的属和种,因此在常规稻田中无法用除草剂控制红米。侵染红米可以使栽培稻的产量降低多达80%。最近,可以使用抗咪唑乙烟的Clearfield(TM)大米技术选择性地控制红米。为了更好地管理红米,需要有关以下方面的信息:(1)由于不同红米生物型而造成的产量损失; (2)栽培稻和红稻生物型之间的互异杂交频率; (3)植物和环境因素对异源杂交率的影响”和(5)上个世纪红米对栽培稻的基因渗入程度。;进行田间和温室试验以检验(1)最大异源杂交的变异性大田开花高峰期间12种红稻生物型与“ CL161”稻之间的比率以及(2)红稻生物型与CL161稻的遗传相容性在田间试验中,红稻生物型与CL161之间的最大异交率为0.03-0.25%。在红色水稻生物型和CL水稻之间的人工杂交中,表明遗传相容性的结实率为49%至94%。大多数红色水稻生物型与CL161水稻具有相似的相容性。确定播种日期,CL品种和红米生物型对异源率的影响。为了进一步了解水稻和红米对异源率的影响,我们还旨在确定相关CL稻和红稻生物型开花时间,气温和相对湿度对异交率的积极贡献。与早期播种相比,后期播种的异交率较低。一般而言,在红米生物型和CLXL8杂交稻之间观察到的异种杂交率高于CL161水稻(0.21%)。红米生物型与CL161的异种率在0至0.21%之间,与CLXL8杂交稻的异种率在0至1.26%之间。在植物和环境因素中,红米类型是影响与CL 161水稻异交率的主要因素。另一方面,对于CLXL8,开花期间的最小相对湿度对异交率的影响最大。还进行了实验,以确定从红米生物型到栽培稻的基因流量,并评估了其形态,物候和繁殖力。导致异形。从杂草稻到栽培稻的基因流率在0.01%至0.2%之间,并且因红稻生物型而异。 CL161水稻与红色水稻之间的F1杂交高138至150 cm,开花时间比CL161水稻晚1至5 d。所有杂交的种子具有红色果皮,短柔毛,成熟时破碎,发芽率> 90%。;进行了田间试验,以评估不同种植日期下红米生物型的出苗方式,并评估红米生物型CL水稻的效果。品种和播种日期对栽培稻产量的损失。红米生物型的出现率随播种日期的增加而增加。一般而言,由于红米生物型导致的CL水稻产量损失在播种后期增加,高达49%。 CL161和CLXL8杂交水稻中,不同红米类型的CL水稻产量损失分别为14%至45%和6%至35%。在以后的种植中,栽培稻与红稻的竞争变得较弱,从而导致更高的产量损失。研究了最近100年间阿肯色州红稻种群的遗传多样性以及这些红稻种群的遗传物质从栽培稻的渗入。使用27个水稻微卫星标记物,对来自阿肯色州四个生态区的一百三十七个红稻品种和上个世纪在阿肯色州种植的36个水稻品种进行了指纹识别。在阿肯色州种植的所有水稻品种形成了与红米品种分开的簇。通常,红米种质分为4组:无芒草皮,黑壳,棕皮和带芒草皮,以及红米生物型与水稻品种之间的一些种质。无芒草皮种质在遗传上与黑壳(GD = 0.55)和棕壳(GD = 0.60)相距遥远。此外,黑壳和棕壳类型在遗传上也比无篷稻草类型更远(GD = 0.96)。黑壳和稻草红色稻米的多样性受其起源地的影响。在上个世纪,阿肯色州25%的红米种质已从栽培稻中渗入了某种遗传物质。

著录项

  • 作者

    Shivrain, Vinod.;

  • 作者单位

    University of Arkansas.;

  • 授予单位 University of Arkansas.;
  • 学科 Agriculture Agronomy.;Agriculture Plant Culture.
  • 学位 Ph.D.
  • 年度 2008
  • 页码 188 p.
  • 总页数 188
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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