大菊品种资源遗传多样性研究
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摘要
菊花(Chrysanthemum×morifolium Ramat.)是菊科(Compositae)菊属(Chrysanthemum)植物,在我国有一千六百多年的栽培历史,是深受人民群众喜爱的传统名花。菊科植物是被子植物中进化程度最高的类群,而由于长期的栽培、自然选择和人工杂交,菊属中的菊花则位于进化的顶点。我国菊花品种数量众多,形态变异丰富,适应性强,分布广泛,遗传背景非常复杂,这些都为菊花品种资源调查、品种分类与鉴定、品种多样性分析等带来了困难,严重限制了菊花的遗传改良进程和园林实践应用。本文对北京地区的大菊品种资源进行了详细的调查,并在控制的栽培条件下,分别在表型和分子水平上对其进行了遗传多样性评价,并对数量性状进行概率分级,筛选出变异幅度及对分类作用最大的性状,期望为菊花品种资源的收集保存及合理利用提供依据,为菊花的品种分类与鉴定、品种保护及育种工作提供一定的参考资料。
     主要研究结果如下:
     1.品种资源调查经调查统计鉴定出北京地区的常见大菊品种1001个,5类瓣型中,平瓣类和管瓣类品种数量最多,分别占总品种数的42%和33%,桂瓣类(2%)较为稀少;在30个花型中,叠球型(205个)、翻卷型(97个)和卷散型(86个)品种数量较多,而管球型和全桂型仅各有一个品种,极为珍贵;在9个色系类型中,品种数量以白色和黄色居多(226个,213个),占44%;红色(29个)、绿色(29个)和橙色(15个)等花色在菊花品种中较为稀少;花色在不同花型中分布不均,在翻卷型、卷散型、钩环型和管盘型4种花型中具有齐全的9类花色,其余26个花型中均存在不同程度的花色缺失现象。调查中还发现:目前生产中仍然存在大量同名异物、同物异名的混杂现象。
     2.数量性状分级选择代表性强的400个大菊品种,参照《菊花DUS测试指南》的形态性状测试方法,检测其18个主要的数量性状,并对性状的分布范围、平均值、变异系数进行统计计算,在此基础上,绘制了分布频次图,结合非参数检验判断性状的分布类型。研究结果表明:叶柄长、叶片长、花径、花梗粗等13个数量性状均符合正态分布,而花瓣宽、节间长、花梗长、舌状小花数和筒状小花数5个数量性状呈现非中心的偏态分布,其中筒状小花数变异情况最为特殊,是严重的偏态分布。在此基瓷?对符合正态分布的13个数量性状进行了概率分级,确定分点值;对其余5个不符合正态分布的性状按照实际测试值分级,并在小于1/10的标准差范围内适度调整,方便其在实际中应用。
     3.质量性状分布参照《菊花DUS测试指南》的形态性状测试方法,观察记录大菊39个主要质量性状的表现,计算各性状的表现式样在品种群内的分布比例,结果显示舌状花的重瓣性、花瓣曲反状况、叶片基部性状、托叶大小等32个性状的表现式样在品种群内分布极不均匀,接近或超过70%的品种集中在性状的1种或2种表现式样中;而花瓣形状、外花瓣表面色、外花瓣背面色、花中心部颜色、叶裂刻基部有无突起、茎的曲直性和茎色等7个性状的表现式样在品种群内的分布则相对均匀。
     4.性状的稳定性及变异计算性状的变异系数,结果表明菊花表型性状均具有较高的多样性,花部性状相对于叶部性状变异系数更高。对22个稳定性状进行R聚类分析发现菊花性状之间相关性不大,大都独立演化。主成分分析结果显示:影响品种分类的第1主成分主要包含舌状小花数、花瓣长、总苞片基部到花顶部的高度、花瓣形状等花部性状;第2主成分主要为两个花色性状(花瓣表面色彩、花瓣背面色彩),第3主成分主要是筒状花部直径、筒状花长度,第4主成分主要是托叶相关性状。
     5.ISSR分子标记研究从50个ISSR引物中筛选出10个条带清晰、重复性良好的引物,对具有典型代表性的150个大菊品种的遗传多样性进行分析。结果共检测清晰可重复的229个位点,其中220个位点是多态性的;多态性位点百分率(PPB)是96.07%,Nei's基因多样性指数(He)和Shannon信息指数(I)分别是0.3485和0.5154;而五个瓣型内的遗传多样性水平都比较高,其中平瓣类的遗传多样性水平最高(PPB=95.20%),而桂瓣类(PPB=86.90%)最低。利用瓣型间的遗传相似系数进行UPGMA聚类分析,结果将瓣型首先分为两大类:平瓣类、管瓣类、匙瓣类、畸瓣类聚在一类中,桂瓣类单独作为一类,在第一类中,平瓣类与管瓣类是最先聚在一起的两种类型,然后是匙瓣类,最后是畸瓣类。
     综合以上的研究结果表明:(1)北京地区现有大量大菊品种,且花型与花色较为丰富;(2)珍稀花型、花色品种亟需保护;(3)大部分数量性状是符合正态分布的,少数重点观赏性状迫于选择压力呈现偏态分布,概率分级法能够辅助大菊的数量性状建立新的分级标准;(4)大部分质量性状在品种群内的分布是不均匀的,可能是由菊花性状遗传分化的不均衡性或受到选育重点性状的连锁作用而造成的;(5)大菊花部性状相对稳定,对品种分类影响较大,其托叶部分也具有一定程度的稳定性,可以作为品种分类的合理补充,而叶部性状稳定性较差,在品种分类中应作为更次一级的分类依据;(6)平瓣类、管瓣类和匙瓣类的亲缘关系最近,畸瓣类品种花瓣先端特化受到人们的喜爱,长期的选择压力使其区别于3种基本瓣型,而这四种瓣型与桂瓣类在亲缘关系上较远;(7)ISSR分子标记检测表明:大菊品种多态性位点百分率较高,平瓣类品种的遗传分化最为丰富。
Chrysanthemum×morifolium Ramat.,which belongs to Chrysanthemum and Compositae,is much loved by Chinese people as a traditional flower with a history of more than one thousand and six hundred years..Since the Compositae is the most advanced group in angiosperm,the cultivars of C. morifolium were deemed to be situated on the peak of the evolution owing to long periods of cultivation, natural selection and artificial crossing.As a result of numerous cultivars,abundant morphological variation,powerful suitability,wide distribution and extremely complicated genetic background,the investigation,classification,identification and diversity analysis of the cultivars became to be very difficulty,which restricted the breeding and landscape application furtherly.On the basis of investigation and identification of the cultivars of large-flowered chrysanthemum in Beijing area,the genetic diversity of phenotypic character and genic differences were analyzed under the condition of controlled cultivation,the system of probability grading for quantitative characters was built and some characters with bigger variation width and greatest impact in classification were screened out in order to provide the basis for collection,preservation and reasonably application and reference for classification, identification,protection and breeding of the cultivars.The main results were as follows:
     1.The investigation of cultivars resource Through the author's survey and record in 6 year,we got 1001 cultivars of large-flowered Chrysanthemum in Beijing.The results of statistic analysis showed: the Flat-petaled Group(42%) and Quilled-petal Group(33%) took the most part of cultivars in the 5 groups,whereas the Anemone-petal group(2%) had even less cultivars.The Globular Types(205), Reflexed Types(97) and Mobile-petaled Types(86) had the most cultivars in 30 flower types,but the Tubular-globular Types and the Whole Anemone Types only had one rare cultivar.The white(226,23%) and the yellow cultivars(213,21%) were the two greatest teams in the 9 groups of flower colors, whereas the red(29),green(29) and orange(15) cultivars were much fewer.The colors distributed in different flower types were unever.Only the Reflexed Types,Mobile-petaled Types,Open bead Types and Tubular-pan Types had all nine colors;all of the other 26 flower types existed deficiency of flower color in various degrees.Additionally,a lot of mistake with homonym and synonym phenomenon still existed in the production..
     2.The probability grading for quantitative characters 400 large-flowered cultivars were chosed and their eighteen chief quantitative characters were tested and recorded according to the test method of morphological characters in the .The empirical distributions were determined by nonparametric test after the distribution range,mean value and variation coefficients of these characters were calculated and frequency diagrams were drawn.The results indicated that 13 quantitative characters(petiole length, leaf length,inflorescence diameter,peduncle diameter and so on) obeyed to the normal distribution, whereas the other 5 characters(floret width,internodes length,peduncle length,number of ray flowers and number of disc flowers) agreed with skewed distribution,in which the number of disc flowers was the most special character with extreme skewness.The grading criterials of the 13 quantitative characters obeyed to the normal distribution were determined with the method of probability grading, the grading criterials of another 5 characters were calculated on the basis of their actual test values. these criterials were moderately adjusted in less than 1/10 of standard deviation for practical application.
     3.The distribution of the qualitative characters The performance of the 39 chief qualitative characters were observed and recorded,according to the test method of morphological characters in the .The results of distribution proportion of each character in cultivars group showed that the distribution of 32 characters(number of ray flower rings,floret curliness,shape of leaf base,size of stipule and so on) were very asymmetrical with near or above 70%cultivars concentrated upon one or two performance, however,the distribution of the other 7 characters(floret type,surface color of outer floret,back color of outer floret,color of disc floret,claw in base of sinus between lateral lobes,stem erectness and stem color) in the cultivars group were relatively symmetrical.
     4.The stability and variation of the characters The results of every character's variation coefficient indicated that they all had higher diversity,the variation coefficient of floral characters is higher than that of foliar.The characters evolved almost independently according to the R cluster analysis of 22 stable characters.The principal component analysis showed that the number of ray flowers, the floret length,height from point of attachment of involucral bracts to top of flower head,floret type and height should be the most important factors.The second principal component contained the surface and back color of outer floret,which followed by the disk flower part diameter and the length of corolla tube. The fourth principal component included some factors about the stipule.
     5.Research of ISSR molecular marker The Genetic Diversity of 150 cultivars with typical representation in large-flowered chrysanthemum were investigated using 10 primers with clear bands and steady repetitiveness chosen from 50 ISSR primers.A total number of 229 bands were amplified,of which 150 were polymorphic loci.The main index were:PPB=96.07%,He=0.3485,I=0.5154(at species level).The genetic variation in each floral types were quite high,in which the Flat-petaled group is highest(PPB=95.20%),whereas the Anemone-petal group(PPB=86.90%) and the Spoon-petaled group(PPB=%9.52%) were the lowest.UPGMA cluster analysis which according to genetic similarity among floral types indicated that 5 groups were clustered into two groups,the Anemone-petal group was one group solely;the other four groups grouped together,in which the Flat-petaled group and the Quilled-petal group clustered firstly,followed by the Spoon-petaled group and the Filiform-petal group.
     The results above showed:(1) The cultivars of large-flowered chrysanthemum are widely distributed in Beijing area with plentiful floral types and floral colors;(2) The cultivars with the rare types and colors are urgent for protection;(3) Most of the quantitative characters obeys to the normal distribution,some important traits agreed with skewed distribution.The probability grading can assist quantitative character in establishing new grading standards;(4) Most of qualitative characters is asymmetrical in cultivars,which might be caused by unbalanced differentiation of characters or linkages coming from emphasis characters selection;(5) The floral characters are relatively stable and have comparably large influence on classification,the characters of stipule also have a certain degree of stability and can act as an reasonable supplement for cultivars classification,but the foliar characters have worse stability and can only be recognized as lower level criterion.(6) The genetic relationship among the Flat-petaled group,the Quilled-petal group and the Spoon-petaled group are closest,which followed by the Filiform-petal group because of long-term selection pressure for the specialization of the petal tip loved by most people.The Anemone-petal group has further genetic relationship with these four groups.(7) ISSR molecular marker detection indicates that the proportion of polymorphic loci of lardge-flowered chrysanthemum is higher,in which the Flat-petaled group has the highest genetic diversity level.
引文
1.白新祥,戴思兰.菊花花色研究进展[J].中国观赏园艺研究进展,2004:131-137.
    2.北海公园管理处.北京栽培菊花的历史[M].北京:中国计量出版社,1999.
    3.北京林学院遗传育种教研组.“菊花的育种”,载园林植物育种学,农业出版社,1962.
    4.北京林业大学园林系花卉教研组.花卉学[M].北京:中国林业出版社,2001.
    5.毕玉芬,卢欣石.植物遗传多样性及种群生态学研究进展[J].甘肃农业大学学报,1999,(1):1-5.
    6.卞阿娜,方份.菊花7个品种过氧化物酶同工酶分析[J].漳州师范学院学报(自然科学版),2003,16(1):78-81.
    7.曹家树,曹寿椿,缪颖,卢刚.中国白菜各类型的分支分析和演化关系研究[J].园艺学报,1997,24(1):35-42.
    8.曹新向.做大开封菊花产业的对策研究[J].甘肃农业,2006,(6):138.
    9.陈发棣,陈佩度,房伟民,李鸿渐.栽培小菊与野生菊间杂交一代的细胞遗传学初步研究[J].园艺学报,1998,(3):308-309.
    10.陈发棣,陈佩度,李鸿渐.几种中国野生菊的染色体组分析及亲缘关系初步研究[J].园艺学报,1996,(1):67-72.
    11.陈发棣,赵宏波,李畅,陈素梅,房伟民.菊属植物细胞学与分子细胞遗传学研究进展[J].南京农业大学学报,2008,(1):118-126.
    12.陈俊愉,程绪珂.中国花经[M].上海:上海文化出版社,1989:122-123.
    13.陈俊愉,梁振强.菊花探源-关于菊花起源的科学实验,科学画报,1964,9:353-354.
    14.陈俊愉,中国梅花的研究Ⅱ.中国梅花的品种分类[J].园艺学报,1962,(3-4):337-350.
    15.陈俊愉.中国花卉品种分类学[M].北京:中国林业出版社,2001.
    16.陈灵芝.中国的生物多样性:现状及其保护对策[M].北京:科学出版社,1999.
    17.程金水.园林植物遗传育种学[M].北京:中国林业出版社,2000,5:258-260.
    18.楚爱香,汤庚国.我国观赏植物的品种分类方法[J].林业科技开发,2008,(4):1-5.
    19.达尔文(著),周建人,叶笃庄,方宗熙(译).物种起源[M].北京:商务印书馆,1995:127-128.
    20.代翠红,李杰,朱延明,纪巍,柏锡.不同DNA提取方法对4种重要作物DNA提取效率的比较[J].东北农业大学学报,2005,(3):329-332.
    21.戴思兰,编著,园林植物遗传学[M].北京:中国林业出版社,2005.
    22.戴思兰,陈俊愉,李文彬.菊花起源的RAPD分析[J].植物学报,1998,(11):1053-1059.
    23.戴思兰,陈俊愉,李文彬.菊属植物RAPD反应体系的建立[J].北京林业大学学报,1996,(1):16-22.
    24.戴思兰,陈俊愉.菊属7个种的人工种间杂交试验[J].北京林业大学学报,1996(4):16-22.
    25.戴思兰,陈俊愉.中国菊属一些种的分支分类学研究[J].武汉植物学研究,1997,15(1): 27-34.
    26.戴思兰,王文奎,黄家平.菊属系统学及菊花起源的研究进展[J].北京林业大学学报,2002,(Z1):230-234.
    27.戴思兰,钟杨,张晓艳.中国菊属部分种的数量分类研究[J].北京林业大学学报,1995,17(4):9-14
    28.戴思兰.中国菊花与世界园艺[J].河北科技师范学院学报,2004,18(3):1-7.
    29.戴思兰.中国栽培菊花起源的综合研究[D].北京:北京林业大学,1994.
    30.邓传良,李存胜,周坚,等.长筒石蒜种质资源的ISSR研究[J].河南师范大学学报(自然科学版),2006,34(1):98-101.
    31.丁兵,王江,赵飞,李玉花.高压静电场在菊花天然杂交种选育中的应用[J].东北林业大学学报,2006,34(2):44-45.
    32.丁广洲,王晓为.作物种质资源的价值及其评估体系的初步构建[J].植物遗传资源学报,2008,9(1):90-95.
    33.丁玲,陈发棣,滕年军,房伟民.菊花品种间过氧化物酶、酯酶同工酶的遗传多样性分析[J].中国农业科学,2008,41(4):1142-1150.
    34.杜欣,董玉芝,陈虹.均匀设计优化喜盐鸢尾ISSR-PCR体系[J].新疆农业科学,2008,45(3):386-392.
    35.段东泰,高全荣.菊花赏鉴与培育[M].北京:农村读物出版社,2002:1-3.
    36.樊冬丽.山西省荞麦品种资源的遗传多样性研究[D].学位论文,山西农业大学,2003.
    37.方开泰.均匀设计—数论方法在试验设计的应用[J].应用数学学报,1980,3(4):363-372.
    38.冯夏莲,何承忠,张志毅,安新民,王冬梅.植物遗传多样性研究方法概述[J].西南林学院学报,2006,26(1):69-74.
    39.傅冰,刘迪秋,李文正,陈丽梅,李昆志.利用ISSR分子标记对25个烟草种质资源的遗传多样性分析[J].安徽农业科学,2008,36(3):898-901.
    40.傅玉兰.寒菊新品种花粉形态特征的研究[J].北京林业大学学报,1998,20(2):110-113.
    41.高爱保.中国瓢虫的物种多样性[J].江西植保,2006,29(1):31-33.
    42.葛颂,洪德元.遗传多样性及其检测方法.见:钱迎倩,马克平主编.生物多样性研究的原理与方法[M].北京:中国科学技术出版社,1994:122-140.
    43.葛颂.植物群体遗传结构研究的回顾和展望.高等教育出版社,1996.
    44.根井正利,著.王家玉,译.分子群体遗传学与进化论.北京:农业出版社,1983:204-244.
    45.顾万春,王棋,游应天.森林遗传资源学概论,北京:中国科学技术出版社,1998.
    46.顾万春著.统计遗传学北京:科学出版社,2004.
    47.观赏园艺卷编委会.中国农业百科全书[M].观赏园艺卷.北京:中国农业出版社,1990.
    48.广西红锥研究协作组.广西红锥适生环境调查[J].广西林业,1984,6(2):56-59.
    49.韩继成,刘庆香,王广鹏,张新忠,孔德军.板栗ISSR反应体系的优化及河北省板栗生态型的分 析[J].河北农业科学,2008,12(4):64-65.
    50.韩洁,胡楠,李玉阁,尚富德.菊花品种资源遗传多样性的AFLP分析[J].园艺学报,2007,34(4):1041-1046.
    51.韩洁.菊花品种资源遗传多样性的AFLP分析[D].开封:河南大学,2007.
    52.郝京辉,游捷,秦贺兰,义鸣放.菊花品种的特异性、一致性和稳定性的研究[J].中南林学院学报,2003,23(5):14-18.
    53.何生根.切花品质的生理生化基础[J].植物生理学通讯,1997,33(1):66-70.
    54.何显静,李标,虞泓.紫斑百合居群生物学研究[J].云南大学学报(自然科学版),2003,25(S1):78-83.
    55.洪德元.植物细胞分类学[M].北京:科学出版社,1990.
    56.胡绍庆,邱英雄,吴光洪.桂花品种的ISSR-PCR分析[J].南京林业大学学报(自然科学版),2004,28(S1):71-75.
    57.胡薇,黄儒珠,孙端,饶春荣,李锦凤.均匀设计优化建兰ISSR-PCR体系[J].生命科学研究,2007,11(1):58-63.
    58.胡志昂.遗传多样性的定义、研究新进展和新概念.生物多样性与人类未来[M],北京:中国林业出版社,1998.
    59.黄芳,黄子杰.均匀设计及其在药学研究中的应用[J].数理医药学杂志,2007,20(5):20-22.
    60.黄家平,戴思兰.中国兰花品种数量分类初探[J].北京林业大学学报,1998,20(2):38-43.
    61.黄家平.栽培小菊部分品种的数量分类研究[D].学位论文,北京:北京林业大学图书馆,2002.
    62.黄建昌,肖艳.γ射线辐照菊花对其遗传性状的影响[J].核农学报,2003,(4):269-272.
    63.黄晓丹,张云贵,应铁进.高质量植物基因组DNA的提取[J].植物生理学通讯,2006,44(2):311-314.
    64.姬君兆,黄玲燕,姬春.菊花[M].北京:中国农业大学出版社,1999.
    65.吉庆萍.有关菊花起源的试验与探讨[D].北京林业大学硕士学位论文,1987.
    66.姜远标,吴涛,陈少瑜,袁瑞玲.思茅松RhPD反应体系的优化[J].东北林业大学学报,2007,35(9):16-19.
    67.金则新,李钧敏,顾奇萍.云锦杜鹃自然居群遗传多样性的ISSR分析[J].园艺学报,2006,33(6):1263-1267.
    68.孔德政,管志涛.基于主成分和聚类分析的荷花品种生物学性状的比较研究[J].中国园林,2008,(8):86-89.
    69.孔庆东,柯卫东,杨宝国.菱白资源分类初探[J].作物品种资源,1994,(4):1-4.
    70.雷武逵.植物遗传多样性的利用及其检测方法[J].广西农学报,2008,23(4):55-58.
    71.类承斌,万勇善,刘风珍.分子标记技术在花生上的应用研究[J].中国农学通报,2005,21(8):36-40.
    72.李畅,陈发棣,赵宏波,陈素梅.栽培小菊17个品种的核型多样性[J].园艺学报,2008,35(1): 71-80.
    73.李畅,陈发棣,赵宏波,房伟民.切花菊14个品种的核形态学研究[J].园艺学报,2007,34(5):1235-1242.
    74.李鸿渐,邵建文.中国菊花品种资源的调查收集和分类[J].南京农业大学学报,1990,13(1):30-36.
    75.李鸿渐.中国菊花[M].南京:江苏科学技术出版社.1993:897.
    76.李建辉,冯永辉,姚永斌.海桐ISSR-PCR反应体系的建立与优化[J].杭州师范学院学报(自然科学版),2007,6(4):288-291.
    77.李茂柏.辽宁省杂草稻遗传多样性研究[D].学位论文,沈阳农业大学,2007.
    78.李懋学,张敩方,陈俊愉.我国某些野生和栽培菊花的细胞学研究[J].园艺学报,1983,10(3):199-205
    79.李懋学,张赞平.作物染色体及其研究技术[M].北京:中国农业出版社,1995.
    80.李萍,石金磊,胡永红,陈醇,蒋昌华,王佳,明凤.凤梨亚科光萼荷属与其近源属亲缘关系的ISSR分子鉴定[J].种子,2007,26(11):35-40.
    81.李强,刘庆昌,翟红,马代夫,王欣,李雪琴,王玉萍.中国甘薯主要亲本遗传多样性的ISSR分析[J].作物学报,2008,34(6):972-977.
    82.李辛雷,陈发棣.菊属野生种、栽培菊花及种间杂种的RAPD分析[J].南京农业大学学报,2004,27(3):29-33.
    83.李运贤,李玉英.植物多样性的分子生物学研究方法[J].南阳师范学院学报,2005,9(4):53.
    84.李真,徐惠梅.菊花品种分类初步研究[J].安徽农学院学报.1989,21(4):282-284.
    85.栗茂腾,余龙江,王丽梅,刘建民,雷呈.菊花花色遗传及花色嵌合体发现[J].遗传,2005,27(6):948-952.
    86.凌良梅,季瑞元,陆占山.菊花杂交育种遗传规律探讨[J].中国菊花研究会论文集,2006:246-251.
    87.刘朝显,眭顺照,郭丽.分子标记在观赏植物研究中的应用[J].现代农业科技,2008,(6):7-8.
    88.刘春迎,王莲英.菊花品种的数量分类研究[J].北京林业大学学报,1995,17(2):79-87.
    89.刘春迎,王莲英.芍药品种的数量分类研究[J].武汉植物学研究,1995,13(2):116-126.
    90.刘华,万建平.均匀试验设计的方法与应用[J].阜阳师范学院学报,2003,20(1):12-16.
    91.刘金萍,车代弟,龚束芳.丰花月季体细胞无性系变异的研究[J].东北农业大学学报,2008,39(7):17-20.
    92.刘孟军.桃树部分经济性状的种内变异及其分级标准研究[J].北京农学院学报,1992,7(2):98-104.
    93.刘孟军.枣树数量性状的概率分级研究[J].园艺学报,1996,23(2):105-109.
    94.刘民,张世红,梁海永,甄志先.部分菊花品种遗传多样性的AFLP分析[J].河北农业大学学报,2008,31(1):48-52.
    95.刘民.利用AFLP分子标记技术对部分菊花品种遗传多样性的研究[D].保定:河北农业大学,2007.
    96.刘平,刘孟军,周俊义,毕平.枣树数量性状的分布类型及其概率分级指标体系[J].林业科学,2003,39(6):77-82.
    97.刘倩倩.中国大菊品种形态分类及细胞学研究[D].北京:北京林业大学,2007.
    98.刘青林,赵会恩.试论观赏植物品种分类的标准与单位[J].北京林业大学学报,1998,20(2):67-71.
    99.刘塔斯,林丽美,龚力民.分子标记中植物DNA提取方法的研究进展[J].中南药学,2005,3(6):370-373.
    100.刘小莉,刘飞虎,李宗菊,曾淑华.10种报春花亲缘关系的ISSR分析[J].云南大学学报(自然科学版),2004,26(5):454-458.
    101.刘祖洞.遗传学(下).北京:高等教育出版社,1991.
    102.龙雅宜.略谈花卉遗传多样性[J].花木盆景(花卉园艺版),2002,5.
    103.龙雅宜.园林植物栽培手册[M].北京:中国林业出版社.2004.
    104.卢华琼,苏智先.部分柚类品种的数量分类和主成分分析[J].安徽农业科学,2006,34(21):5510-5511.
    105.罗晓莹,庄雪影,杨跃生.杜鹃红山茶遗传多样性的ISSR分析(英文)[J].热带亚热带植物学报,2007,15(2):93-100.
    106.罗瑜萍,龚维,邱英雄.羊蹄甲属3种园艺树种分子鉴定及亲缘关系的ISSR分析[J].园艺学报,2006,33(2):433-436.
    107.雒新艳,戴思兰.切花菊新品种DUS测试技术与方法[J].中国观赏植物研究进展.中国林业出版社.2006,7:572-577.
    108.马克平.试论生物多样性的概念[J].生物多样性,1993,1(1):20-22.
    109.麦克尼利等著.1900.李文军等译.1992,保护世界的生物多样性.中国的生物多样性[M].北京科学出版社,99-113.
    110.毛汉书,马燕,王忠芝.中国梅花品种的数量分类研究[J].北京林业大学学报,1992,14(4):59-66.
    111.毛静.中国传统菊花文化研究[D].学位论文,华中农业大学,2006.
    112.缪恒彬,陈发棣,赵宏波.85个大菊品种遗传关系的ISSR分析[J].园艺学报,2007,34(5):1243-1248.
    113.穆立蔷.紫椴ISSR-PCR反应体系的建立与优化[J].林业科学,2006,42(6):26-31.
    114.倪月荷,汪觉先.菊花栽培与鉴赏[M].上海:上海科学技术出版社,2000.
    115.宁慧娟,戴思兰.我国切花菊消费现状的调查及前景预测[J].中国观赏园艺研究进展,2005:583-587.
    116.潘铭,吴子恺.作物数量性状遗传基础知识[J].新疆农业科学,1984,21(1):35-38.
    117.乔玉山,章镇,房经贵,沈志军,赵密珍.李种质资源ISSR反应体系的建立[J].果树学报,2003,20(4):270-274.
    118.秦贺兰,游捷,高俊平.菊花18个品种的RAPD分析[J].园艺学报,2002,29(5):488-490.
    119.邱芳,付健民,金得敏.王斌.遗传多样性的分子检测.生物多样性,1998,6(2):143-150.
    120.邱英雄,傅承新,何云芳.乐昌含笑不同类型鉴定的ISSR-PCR分析[J].林业科学,2002,38(6):49-52.
    121.邱英雄,胡绍庆,陈跃磊.ISSR-PCR技术在桂花品种分类研究中的应用[J].园艺学报,2004,31(4):529-532.
    122.全国菊花品种分类(中国园艺学会花卉盆景协会菊花品种分类学术讨论会会议纪要).中国菊花研究论文集,1990-1992.
    123.阮晓赛,林新春,娄永峰.毛竹种源遗传多样性的AFLP和ISSR分析[J].浙江林业科技,2008,28(2):29-33.
    124.沈德绪.果树育种学[M].北京:中国农业出版社,1998.
    125.沈浩,刘登义.遗传多样性概述[J].生物学杂志,2001,18(3):4-7.
    126.沈永宝,施季森,赵洪亮.利用ISSR-DNA标记鉴定主要银杏栽培品种[J].林业科学,2005,41(1):202-204.
    127.施立明,贾旭,胡志昂,1993.遗传多样性[A].见:陈灵芝,中国的生物多样性[M].北京:科学出版社,31-113.
    128.史刚荣.木槿的发育可塑性及种下分类研究[J].植物研究,2003,23(3):340-344.
    129.思彬彬,杨卓.ISSR标记技术及其在果树遗传育种中的应用[J].安徽农学通报,2008,14(13):116-117.
    130.宿红艳,王磊,明永飞,刘林德.ISSR分子标记技术在金针菇菌株鉴别中的应用[J].生态学杂志,2008,27(10):1725-1728.
    131.孙浩元,杨丽,张俊环,王玉柱.杏种质资源部分数量性状的分级指标探讨[J].中国农学通报,2008,24(1):147-151.
    132.孙洪,程静,詹克慧,张相武,杨艳会.ISSR标记技术及其在作物遗传育种中的应用[J].分子植物育种,2005,3(1):123-127.
    133.孙晋科.巴旦杏RAPD-PCR反应体系的正交优化[J].新疆农业科学,2007,44(5):715-719.
    134.索志立,张会金,张治明.紫斑牡丹与牡丹种间杂交后代的DNA分子证据[J].云南植物研究,2005,27(1):42-28.
    135.索志立,周世良,张会金.杨山牡丹和牡丹种间杂交后代的DNA分子证据[J].林业科学研究,2004,17(6):700-705.
    136.汤忠皓.中国菊花品种分类的探讨[J].园艺学报,1963,2(4):441-418.
    137.陶玲,刘志学,何兴东,刘新民.用于RAPD分析的沙拐枣DNA提取方法[J].中国沙漠,2001,21(3):300-302.
    138.王成树,李增智,分子数据的遗传多样性分析方法(综述).安徽农业大学学报,2002,29(1):90.
    139.王洪新,胡志昂.植物的繁育系统、遗传结构和遗传多样性保护[J].生物多样性,1996,4(2):92-96.
    140.王建波.ISSR分子标记及其在植物遗传学研究中的应用[J].遗传,2002,24(5):613-616.
    141.王力荣,朱更瑞,方伟超.桃种质资源若干植物学数量性状描述指标探讨[J].中国农业科学,2005,38(4):770-776.
    142.王彭伟,陈俊愉.地被菊新品种选育研究[J].园艺学报,1990,17(8):223-228.
    143.王伟,戴华国,陈发棣,郭维明.菊花花部特征及花冠精油组分与访花昆虫的相关性[J].植物生态学报,2008,32(4):776-785.
    144.王文奎.菊花起源的染色体原位杂交研究[D].学位论文,北京:北京林业大学图书馆,2000.
    145.王鑫,敖红,王秋玉.红皮云杉与嫩江云杉RAPD和ISSR分子标记反应体系优化和特异性检测[J].植物研究,2008,28(4):417-421.
    146.王子凡.中国古代菊花谱录存世现状及主要内容的考证[J].自然科学史研究.2009,28(1):77-90.
    147.韦霄,韦记青,蒋水元,蒋运生,唐辉,叶万辉.迁地保护的金花茶遗传多样性评价[J].广西植物,2005,25(3):215-218.
    148.吴国盛,陈发棣,陈素梅,赵宏波,房伟民.基于PCR-RFLP多态的部分菊属与亚菊属植物亲缘关系研究[J].江苏农业科学,2008,(2):58-61.
    149.吴晓梅,杨盛昌,缪颖,陈德海.花卉基因工程研究进展.福建农林大学学报(自然科学版),2003,32(3):325-330.
    150.吴应详.菊花[M].北京:金盾出版社,1991:7-11.
    151.吴在生,李海龙,刘建辉,左志锐,田瑞昌.65个菊花栽培品种遗传多样性的AFLP分析[J].南京林业大学学报(自然科学版),2007,31(5):67-70.
    152.吴振兴,王慧中,施农农.兰属Cymbidium植物ISSR遗传多样性分析[J].遗传,2008,30(5):627-632.
    153.夏铭.遗传多样性研究进展[J].生态学杂志,1999,18(3):59-65.
    154.肖海峻,孟利前,李玉冰.ISSR分子标记及其在植物遗传育种中的应用[J].内蒙古农业科技,2006,(4):31-33.
    155.谢吉容,梁国鲁,李树发.月季‘金银岛'的红花芽变品系的分析鉴定[J].北方园艺,2007,(11):186-188.
    156.谢一青,黄儒珠,李志真,杨宗武,陈杰.光皮桦RAPD分析体系优化设计方案比较[J].福建林学院学报,2006,26(1):73-77.
    157.徐克学.数量分类学[M].北京:科学出版社,1994.
    158.徐文辉,高海卿,陈华进.菊花某些性状遗传规律的初步探讨[J].浙江林学院学报,2000, 17(1):37-41.
    159.许丽,李玥莹,林凤.DNA分子标记及其在作物遗传育种中的应用[J].沈阳师范大学学报(自然科学版),2006,24(4):466-469.
    160.许莹修,戴思兰.菊花品种表型性状分类价值研究[J].中国菊花研究论文集.北京:108-115.
    161.许莹修.菊花形态性状多样性和品种分类的研究[D].学位论文,北京:北京林业大学图书馆,2005.
    162.薛麒麟,郭继红,郭建平.切花栽培技术[M].上海:上海科学技术出版社,2007.
    163.薛守纪.中国菊花图谱[M].北京:中国林业出版社,2004.
    164.杨朝东,王健,张俊卫,张波,包满珠.梅花不同样本间亲缘关系的AFLP初步分析[J].中国农业科学,2005,38(10):2084-2089.
    165.杨传平,潘华,魏志刚,姜静.白桦ISSR-PCR反应体系的优化[J].东北林业大学学报.2005,33(6):1-3.
    166.杨俊宝,彭正松,杨军,赵梅,朱秀志.半夏基因组DNA的提取及鉴定[J].现代中药研究与实践,2006,20(3):26-29.
    167.杨俊霞,郭宝林.桑树数量性状的概率分级研究[J].蚕业科学,1998,24(2):122-124.
    168.杨雷,杨莉,李莉,孙立祎,郝保春.草莓种质资源果实主要数量性状变异及概率分级[J].西南农业学报,2007,20(5):1067-1069.
    169.杨雷,周俊义,刘平,赵智慧,杨莉,李莉,郝保春.酸枣种质资源果实主要数量性状变异及概率分级[J].河北农业大学学报,2006,29(1):34-37.
    170.杨秋,唐岱,苏腾伟,孙晓佳,颜隽.昆明市区菊花资源调查研究[J].福建林业科技,2006,33(3):123-126.
    171.杨淑达,施苏华,龚洵.滇牡丹遗传多样性的ISSR分析[J].生物多样性,2005,13(2):105-111.
    172.杨秀坚,罗富英,窦萍珍.植物调节剂对菊花观赏性状及相关特性的影响[J].北方园艺,2006,(1):45-46.
    173.杨雨,尚富德.开封地区菊花资源调查研究[J].河南大学学报(自然科学版),2008,38(3):293-295.
    174.杨玉玲,马祥庆,张木清.ISSR分子标记及其在树木遗传育种研究中的应用[J].亚热带农业研究,2006,2(1):18-24.
    175.姚毓璆.菊花[M].北京,中国建筑工业出版社,1984.
    176.于恒秀,王淼,梁国华.ISSR引物鉴定芍药栽培品种之间亲缘关系的初步研究[J].植物生理学通讯,2006,42(2):271-274.
    177.余家林.农业多元实验统计[M].北京:北京农业大学出版社,1993.
    178.余艳,陈海山,葛学辉.简单重复序列区间(ISSR)引物反应条件优化与筛选[J].热带亚热带植物学报,2003,11(1):15-19.
    179.张春英,戴思兰,张秀英.RAPD技术及其在花卉育种中的应用[J]中国园林,1999,15(6):36-37.
    180.张春英,戴思兰.我国观赏植物亲缘关系的研究现状[J].北京林业大学学报,1998,20(2):79-84.
    181.张飞,房伟民,陈发棣,赵宏波,贾文珂.切花菊花器性状的遗传变异与相关性研究[J].浙江林学院学报,2008,(3):293-297.
    182.张广进,赵兰勇,王芬.蔷薇品种的数量分类学研究[J].山东农业大学学报(自然科学版),2006,37(2):175-180.
    183.张莉俊,戴思兰.菊花种质资源研究进展[J].植物学报,2009,44(3)(已接受).
    184.张莉俊,秦红梅,王敏,戴思兰.二月兰形态性状的变异分析[J].生物多样性,2005,13(6):535-545.
    185.张莉俊.二月兰遗传多样性研究[D].学位论文,北京:北京林业大学图书馆,2007.
    186.张立荣,刘大群,徐大庆,杨文香,孔俊英.小麦ISSR分析初探[J].河北农业大学学报,2004,27(1):10-13.
    187.张录强.品种资源危机[J].资源与人居环境,2006,(9):34-37.
    188.张敏,黄苏珍,仇硕.鸢尾属植物遗传多样性的RAPD和ISSR分析[J].植物资源与环境学报,2007,16(2).6-11.
    189.张树林.菊花品种分类的研究[J].园艺学报,1965,4(1):35-48.
    190.张宇和.观赏植物遗传多样性及品种分类浅谈[J].北京林业大学学报,1998,20(2):6-11.
    191.赵爱莲.片断森林中红凉伞种群的遗传结构[D].学位论文,华东师范大学,2005.
    192.赵凯歌,虞江,晋芳,陈龙清.蜡梅品种的数量分类和主成分分析[J].北京林业大学学报,2004,26(S1):80-83.
    193.赵丽娟,张宗文,黎裕,王天宇.苦荞种质资源遗传多样性的ISSR分析[J].植物遗传资源学报,2006,7(2):159-164.
    194.赵谦,杜虹,庄东红.14个蝴蝶兰品种遗传关系的ISSR分析[J].植物研究,2008,28(2):227-231.
    195.赵燕,郑丽,李文祥.中国菊花过氧化物酶同工酶分类与自然分类比较.云南农业大学学报,1996,11(2):86-90.
    196.中国作物遗传资源[M].北京:中国农业出版社,1994.
    197.中华人民共和国农业部.植物新品种特异性、一致性和稳定性的测试指南(菊花).2002,10.
    198.钟金城,赵素君,陈智华,马志杰.牦牛品种的遗传多样性及其分类研究[J].中国农业科学,2006,39(2):389-397.
    199.周春玲,戴思兰.部分菊属植物的AFLP分析.北京林业大学学报,2002,24(5-6):71-75.
    200.周家琪.牡丹、芍药花型分类的探讨[J].园艺学报,1962,1(3-4):351-360.
    201.周树军,汪劲武.10种菊属(Dendranthema)植物的细胞学研究[J].武汉植物学研 究,1997,15(4):289-292.
    202.周延清.DNA分子标记技术在植物研究中的应用[M].北京:化学工业出版社,2005.
    203.竺利波,顾万春,李斌.花灌木种质资源及其遗传多样性研究[J].植物遗传资源学报,2007,8(2):240-245.
    204.邹喻萍,葛颂,王晓东.系统与进化植物学中的分子标记.北京:科学出版社,2001:3-9.
    205.Abd El-Twab M.H.and Kondo K.Identification of mutation and homologous chromosomes in four cultivars of Dendranthema grandiflora by physical mapping of 5S and 45S rDNA using fluorescence genomic in situ hybridization[J].Chrom.Sci.2004,8:81-86.
    206.Boronnikova S.V.,Kokaeva Z.G.,Gostimsky S.A.,et al.Analysis of DNA polymorphism in a relict Uralian species,large-flowered foxglove(Digitalis grandiflora Mill.),using RAPD and ISSR markers[J].Russian Journal of Genetics.2007,43:5,530-535.
    207.Bosten D.,White R.L.,Skolnick M.,et al.Construction of a genetic linkage map in man using restriction fragment polymorphism[J].Am J Hum Cenet,1980,32:314-331.
    208.Brooks R.R.,Shaw S.,Marfil A.A.The chemical form and physiological function of nickel in some Iberian Alyssum species Physiol[J].Planta,1981,51:161-170.
    209.Bryan G.T.,Wu K.,Farrall L.,et al.A single amino acid difference distinguishes resistant and susceptible alleles of the rice blast resistance gene Pi-ta[J].Plant Cell,2000,12:2033-2045.
    210.CHEN F.H.Origin of Chinese Chrysanthemum[J].The Chrysanthemum and Dahlia,1957(7):264-265.
    211.CHEN J.Y.Studies on the origin of Chinese florist' s chrysanthemum[J].Acta Hort,1985(167):349-361.
    212.Dai S.L.,Wang W.K.,Li M.X.Phylogenetic Relationship among Dendranthema(DC.) Des Moul.Revealed by Flourecence In Situ Hybridization[J].Journal of Integrative Plant Biology,2005,47(7):783-791.
    213.Devos K.M.and Gale M.D.The use of random amplified polymorphic DNA markers in wheat,Theor.Appl.Genet,1992,84:567-572.
    214.Dowrick G.J.Chromosomes of chrysanthemum(Ⅰ) The species[J].Heredity,1952.6:365-375.
    215.Dowrick G.J.The chromosomes of chrysanthemum(Ⅱ)Garden varieties[J].Heredity,1953.7(3):59-72.
    216.Doyle J.J.and Doyle J K.A rapid DNA isolation procedure for small quantites of fresh leaf tissue[J].Phytochemical Bulletin,1987,19:11-15.
    217.Endo M.and Inada I.The appearance of sports and chromosome number variations in the Japanese garden chrysanthemum,Chrysanthemum morifolium Ramat[J].Japan Soc Hort Sci,1992,61(2):389-398.
    218.Endo M.On the occurrence of B chromosome in the garden chrysanthemum,Chrysanthemum morifolium Ramat[J].Japan Soc Hort Sci,1990,59(3):613-620.
    219.Endo N,Inada I.On the karyotypes of garden chrysanthemums,Chrysanthemum mori folium Ramat[J].Japan Soc Hort Sci,1992,61(2):413-420.
    220.Endo N.The chromosome survey on the cultivated chrysanthemums,Chrysanthemum morifoliurn Ram.Ⅱ.On the chromosome numbers of cultivated chrysanthemum(Part 1)[J].Japan Soc Hort Sci,1969,38(4):343-349.
    221.Falconer D.S.Introduction to quantitative genetics(3~(rd) ed.)[M],New York:Longman Scientific and Technical,1989.
    222.Fang D.,Krueger R.R.,Roose M.L.Phylogenetic relationships among selected Citrus germplasm accessions revealed by inter-simple sequence repeats(ISSR)markers[J].Amer Soc Hort Sci,1998,123(4):612-617.
    223.G J.,El-Bayoumi A.The origin of new forms of the garden chrysanthemum[J].Euphytica,1966(15):32-50.
    224.Gottlieb L.D.Electrophoresis evidence and plant populations[M].Progress in Phytochemistry[C].Pergamon:Oxyford University Press Ine,1981.1-66.
    225.Gupta M,Chyi Y S,Romero-Sevenson J,Owen J L.Amplification of DNA marker from evolutionarily diverse genomes using single primers of simple-squence repeats[J].Theor App.Genet,1994,89:998-1006.
    226.Hartl D.L.,Clark A.G.Principles of Population Genetics(2~(nd) ed)[M].Sunderland M A:Sinauer Associates,1989.
    227.Huang J.C.,Tanabe K.,Itai A.Identification of flowering lotus cultivars by ISSR (inter-simple sequence repeat) markers[J].Horticultural Research(Japan).2003,2:4,259-264.17.
    228.Huang S.C.,Tsai C.C.,Sheu C.S.Genetic analysis of chrysanthemum hybrids based on RAPD molecular makers[J].Botanical Bulletin of Academia Sinica,2000,41:257-262.
    229.International Union for the Protection of New Plant Varieties(UPOV).Guidelines for the conduct of tests for distinctness,homogeneity and stability,Chrysanthemum spec.TG/26/4.
    230.Jackson J.A.,Matthews D.,Cooper W.,et al.Investigation of microsatellite profiling for DUS testing in chrysanthemum[J].Acta Hort.521.ISHS 2000:243-253.
    231.Kaneko K.Cytogenetical studies on three high polyploidy species of Chrysanthemum [J].J Sci.Nort.Univ.Series B,Div.1961.2(9):59-98.
    232.Karp A.,Edwards K.J.DNA markers:a global overview // Caetano-Anolles G,Gressh off PM.DNA Markers Protocols,Applications,and Overviews[M].New York:Wiley-Liss,Inc,1997:1-13.
    233.Kim J.Y.,Hong Y.P.,Han I.S.Studies on the native Chrysanthemum spp.in Koera:1,Studies on the characteristics,geographical distribution and line selections of wild grown Chrysanthemum zawadskii in Korea[J].Research Reports of the Rural Development.Administration(Suweon),1989.31(2 Hortic):59-66.
    234.Kim S.H.,Huh M.K.,Lee J.H.Genetic relationships of among taxa of genus Sorbus based on ISSR marker analysis.[J]Miskininkyste.2007.1(61):69-75.
    235.Lefebrve V.,Palloix A.,Rives M.,et al.Nuclear RFLP between pepper cultivars (Capsicum annuurn)[J].Earpy Ytytica.1992,71(3):189-199.
    236.Marshall D.R.Crop genetic resources:current and emerging issues,in Plant Population Genetics[M],Breeding and Genetic Resources,1990:367-388.
    237.Meyer W.,T G.,Mitchell E.Z.Freedman & R.Vilgays.Hybridization probes for conventional DNA fingerprinting used as single primers in the polymerase chain reaction to distinguish strains of Cryptococcus neoformans[J].J Clin Microbiol 1993(31):2274- 2280.
    238.Moreno S.,Martin J.P.Ortiz J.M.ISSR-PCR for characterization of closely related grape vine germplasm[J].Euphytica,1998,101:117-125.
    239.Nazzer M.A.and Khoshoo T.N.Variation in The chromosome complement of Chrysanthemum morifolium cmoplex[J].Nucleus,1983,26:22-29.
    240.Nei M.Analysis of gene diversity in subdivided populations.Proc Natl Acad Sci USA,1973.70(12):3321-3323.
    241.Quinn G.P.and Keough M.J.著.蒋志刚,李春旺,曾岩译.生物实验设计与数据分析.北京:高等教育出版社,2003:163-180.
    242.Rafalski J.A.,Tingey S.V.,Williams J.G.K.,RAPD markers-a new technology for genetic mapping and plant breeding[J],Ag.Biotech.News.Inf.,1991,(3):645-648.
    243.Rohlf F.J.NTSYS-pc.Numerical Taxonomy and Multivariate Analysis System,Version 2.I.Exeter Software[M].New York:Setautket.2000.
    244.Rout G.R.,Senapati S.K.,Aparajita S.Studies on the genetic relationship among 13cultivars of Calathea(Marantaceae) using RAPD and ISSR markers[J].Advances in Horticultural Science.2007,(21):3,147-155.27.
    245.Roxas N.J.L.,Tashiro Y.,Miyazaki S.,et al.Isozyme analysis in Higo chrysanthemum (Dendranthema grandiflora Tzvelev)[J].Journal of Japanese Society for Horticultural Science,1993,61(4):919-924.
    246.Rzepka-Plevnes D.,Smolik M.,Tanska K.Genetic similarity of chosen Syringa species determined by the ISSR-PCR technique[J].Dendrobiology.2006.56:61-67.22.
    247.Sanchez G.,Goodman M.M.,Rawlings J.O.Appropriate characters for racial classification in maize[J].Econ.Bot.1993,47:44-59.
    248.Schaal B.A.,Leverich W.J.,Rogstad S.H.Comparison of methods for assessing genetic vatiation in plant conservation biology[M].In Falk,D.A.and K.E.Holsinger(eds.).Genetics and Conservation of Rare Plants.New York:Oxford University Press,1991.123-134.
    249.Sokal,R.R.Statistical methods in systemetics[J].Biol.Rev.Cnmbr.Phil.Sec.1965,40:337-391.
    250.Solbrig O.T.(ed.).Form genes to ecosystems a research agenda for biodiversity IUBS Psris.1991.
    251.Soltis P.S..Soltis D.E.Genetic variation in endemic and widespread plant species:examples from Saxifragaceae and Polyslichum[J],Aliso,1991,13:215-223.
    252.Tahara M.Cytological studies on Chrysanthemum(A preliminary note)[J].BotMag Tokyo,1915,29:48-50.
    253.Talhinhas P.,Neves-Martins J.,Leitao J.Inter-and intra-specif ic genetic diversity in Lupinusevaluated with AFLP,ISSR,and RAPD markers.[B]Wild and cultivated lupins from the Tropics to the Poles.Proceedings of the 10th International Lupin Conference,Laugarvatn,Iceland,19-24 June 2002.2004.7-9.9.
    254.Tanaka R.On the speciation and karyotypes in diploid and tetraploid species of Chrysanthemum(V) Chrysanthemum yoshinaganthum(2n-36)[J].Cytologia,1960.25:43-58.
    255.Wang C.Y.Evaluation of genetic diversity of chrysanthemum using AFLP markers[J].Dutch-Chinese Life Science Forum,Wagenningen,The Netherlands,2003.
    256.Wang W.K.,Dai S.L.,Li M.X.Physical mapping of rDNA in Dendranthema nankingense and its close related species by Florecent in situ hybridization[J].Cellular & Molecular Biology Letters.2002,(7):911-914.
    257.Wang W.K.,Li M.X.,Xu Y.X.,et al.Several Influencing Factors on Fluorescent in situ Hybridization Experimental System Applied to Dendranthema spp[J].Forestry Study in China,2003,5(2):30-34.
    258.Wang Z.Y.,Zhuang G.Z.,Fan M.R.Comparative analysis of genetic similarity among Anthurium cultivars by using ISSR and RAPD markers[J].Journal of Agricultural Research of China.2001.50:1,54-67.48.
    259.Weir B.S.Genetic data analysis[M].Sunderland,M.A:Sinauer Assoc.1990.260.William C.E.and Claim D.A.Phenetic relationships and levels of variability detected by restriction fragment length polymorphism and random amplified Plymorphic DNA analysis of cultivated and wild accessions of Lycopersicon esculentum[J].Genome.1993,36(3):619-630.
    261.Wilson E.O.ed.Biodiversity,National Academy Press,Washington D.C.1988.
    262.Wu K..Jones R.,Dannaeberger L.,et al.Detection of microsatellite polymorphisms without cloning[J].Nucleic Acids Res.1994,(22):3257-3258.
    263.Yeh F.C.,Yang R.C.,Boyle T.POPGENE Versionl.31,Microsoft Window-based Freeware for Population Genetic Analysis[M].University of Alberta and Centre for International Forestry Research.1999.
    264.Zabeau M.and Vos P.Selective restricition fragment amplification,a:general method for DNA fingerprintings.European patent Applification.(Publication No:0534858Al)[M].Paris.-European office.1993.
    265.Ziekiewica E.,Ratalski A.,Labuda D.Genome fingerprinting by simple sequence repeat(SSR)-anchored polymerase chain reaction amplification[J].Genomics.1994,20:176-183.

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