东北地区野生百合种质资源及遗传多样性研究
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
百合是百合科(Liliaceae)百合属(Lilium)多年生球根草本花卉,世界五大鲜切花之一,其花朵硕大、花色艳丽、花姿百态、芳香怡人,世界各地广为栽培,在世界鲜切花市场上占有十分重要的地位。我国野生百合资源十分丰富,约有55个种,其中36个种、15个变种为特有种,但是大部分野生资源没有得到充分利用,且破坏流失严重、多样性逐渐下降。本论文对东北地区野生百合资源进行调查和收集,并采用形态学、孢粉学、细胞学和RAPD标记对收集的百合资源进行亲缘关系和遗传多样性研究,为东北地区野生百合资源的收集、保存、保护、分类、评价、利用等奠定基础。主要结果如下:
     对东北地区野生百合种质资源进行考察与收集,共收集野生百合119份,分属6种3变种,包括卷丹25份、细叶百合15份、毛百合12份、垂花百合2份、朝鲜百合7份、东北百合7份、有斑百合40份、大花百合3份、大花卷丹8份,考察与收集过程中未发现条叶百合。其中,有斑百合和卷丹在东北地区分布范围最广、分布数量最多,尤其在铁岭、本溪等地分布较多;其次是细叶百合,分布较广泛;而垂花百合和大花百合分布范围比较狭窄,收集到资源份数较少,垂花百合仅在凤城和抚顺收集到2份资源,大花百合仅在铁岭和蛟河收集到3份;而朝鲜百合分布范围则比较集中,仅分布于靠近朝鲜的丹东地区。采用AHP法对野生百合进行综合评价,并依据最终得分情况,将所有种类分为3个等级。卷丹和垂花百合分值最高,为第Ⅰ级,应在保护的前提下加强开发力度;细叶百合有斑百合、大花卷丹和朝鲜百合处于第Ⅱ级;东北百合、毛百合和大花百合处于第Ⅲ级。虽然东北百合、毛百合和大花百合分值较低,处于第Ⅲ级,但并不代表它们没有利用价值,相反,它们均有各自的优良性状,因此应注重有目的的开发和利用。
     对50份野生百合资源的16个主要形态性状进行统计分析,结果表明,东北地区野生百合种质资源的主要性状有明显差异,表现出显著的形态多样性。各形态性状的变异系数除了叶长的变异系数相对较小,为23.35%,其他性状的变异系数都大于25%,其中花柱长和叶宽的变异系数较大,分别为64.57%和59.37%;野生百合形态多样性指数均较高,平均多样性指数达2.66,这表明东北地区野生百合种间各性状分化程度较大,其中叶长、内花瓣宽的多样性指数较高,分别为2.87和2.88。东北地区野生百合种质资源形态性状的主成分明显,前四个主成分方差累计贡献率达到了87.51%,包含了24个性状指标的87.51%的信息,基本能代表这24个性状的变异。在24个形态性状中,外轮花瓣宽、内轮花瓣长、内轮花瓣宽、花被片颜色、花型、花梗长、叶长是引起形态变异的主要性状,这一结论与形态多样性指数得出的结论相一致。利用DPS数据统计软件,将50份野生百合种质资源的形态数据进行聚类,50份材料被聚为三大类,第一类30份材料,包括花朵相对较小的种类:细叶百合、有斑百合、大花百合、朝鲜百合和垂花百合;第二类19份材料,包括茎叶粗壮、花朵较大的种类:卷丹、大花卷丹和毛百合;第三类包括东北百合,为轮叶组百合。
     利用光学显微镜和电子显微镜观察野生百合花粉形态及表面纹饰。百合的花粉形态均以单粒形式存在,对称性较强,赤道面观呈舟形,具单萌发沟且沟延伸至两极;极面观为椭圆形,边缘具萌发沟。对极轴、赤道轴、极轴/赤道轴3个指标进行方差分析,结果表明3个指标在种间均达到极显著差异。以极轴/赤道轴进行多重比较,结果表明,部分百合种存在显著或极显著差异,但也有部分百合种间差异不显著。种内差异显著性分析表明,不同来源间表现一致的只有朝鲜百合,极轴、赤道轴和极轴/赤道轴三个性状在种内未达到显著差异;而不同来源的卷丹和细叶百合的花粉各指标都达到极显著,存在差异。东北地区百合花粉表面纹饰基本类型为网状,网脊盘珠状或瘤状颗粒,形成多边形或不规则网眼。网眼的大小及分布密度和网脊上颗粒大小及密度在种间有一定的差异。在扫描电镜下观察,一般在近极面中部网眼最大,向两端或沟边缘渐变小。
     对染色体制片技术的取样时间、预处理液、解离时间、染色剂等方面进行试验研究,结果表明,根尖取样时间以上午8:30-9:30为佳,用0.1%秋水仙碱溶液4℃下预处理24 h,经卡诺固定液固定6 h后,在1 m01·L-1盐酸60℃下恒温水浴中解离5 min(卷丹为8 min),改良卡宝品红溶液染色压片镜检,能取得良好的制片效果。东北地区9种野生百合染色体为大型染色体,除卷丹为三倍体外,其他种均为二倍体,核型特征均由两对具中部(m)或具近中部(sm)着丝点的大型染色体以及10对具近端部(st)和端部(t)着丝点染色体所组成。种间的差异主要表现在各不同类型染色体的数目以及它们在核型中排序位置的差异,其次是随体的数目和位置的不同。核型分类除毛百合属于3A型,其它都属于3B型。在观察的百合根尖细胞中,除正常的染色体数目外,还存在少数体细胞染色体数目不同程度的变异,但是出现变异的频率较低。东北百合在观察的30个细胞中,没有发现染色体数目变异,其他种均发现染色体数目的变异,卷丹染色体数目变异范围较大,约占所观察细胞(100个)的11%,而且还观察有单倍体细胞(2n=x=12)出现,约占2%。在卷丹、细叶百合、毛百合、有斑百合、大花百合5种百合的根尖细胞中观察到B染色体,卷丹、有斑百合和大花百合的根尖细胞中观察到1条B染色体存在,毛百合根尖细胞中发现2条B染色体,而在细叶百合的根尖细胞中观察到有1条或2条B染色体存在,且出现频率较高,占观察细胞总数(100)的10%。
     用12个RAPD随机引物对50份野生百合试材进行扩增,共扩增出105条清晰谱带,其中86条为多态性谱带,多态率为81.8%,平均每个引物扩增出7.2条多态性谱带,表明东北地区野生百合之间具有丰富的遗传多样性。而且,大部分引物在不同试材上都具有主特征带,这反映了百合属内基因组的同一性。基于50份野生百合资源之间欧氏距离的矩阵,利用UPGMA进行了聚类分析。从聚类结果可以看出,供试的50份百合资源可分为两大类:第一类包括供试的38份试材,包括大花卷丹、卷丹、毛百合、朝鲜百合、东北百合、有斑百合和大花百合;第二类包括细叶百合和垂花百合,共12份试材。第一类又可以分为2个亚类,第一亚类包括大花卷丹、毛百合、朝鲜百合、东北百合4个种(变种);第二亚类包括卷丹、有斑百合、大花百合3个种。聚类结果表明,卷丹与有斑百合的亲缘关系较近,而与同为卷瓣组的朝鲜百合、细叶百合、大花卷丹等亲缘关系较远;垂花百合与细叶百合亲缘关系较近。
Lilium, a perennial bulbous flower belonging to the Liliaceae, is one of the five most important cut flowers.With its big and colorful flower, beautiful stature and fragrance, it is cultured extensively worldwide and paly an important role in the floral market. In China, there are abundant wild resources of Lilium with a total of 55 species, in which 36 species and 15 varieties are native species. But many of them have yet not been used, and a great number of precious resources are endangering because of natural disasters. Therefore, in this paper, 119 wild Lilium resources native to Northeast China were investigated and collected, and the genetic relationship and diversity were studied at morphological, palynological, cytological and molecular level, which lay a foundation for the collection, preservation, conservation, classification, evaluation and utilization of wild Lilium species. The results were as follows.
     119 accessions resources of wild Lilium germplasm were collected native to Northeast China. The germplasm accessions collected.were classified into 6 species and 3 varieties, including 25 Lilium lancifolium Thunb.,15 L. pumilum DC.,12 L. dauricum Ker-Gawl,2 L. cernuum Komar.,7 L. amabile Palib.,7 L. distichum Nakai,40 L. concolor Salisb. var. buschianum (Lodd.) Baker,3 L. concolor Salisb. var. megalanthum Wang et Tang,8 L. leichtlinii Hook.f. var. maximowiczii (Regel) Baker. But L. callosum Sieb. has not been collected until now. Based on the geographical distribution, L. concolor var. buschianum was believed to be the most widely distributed species, and it was collected from 16 cities in the northeastern region. L. lancifolium was one of the most widespread species with high adaptability in China, and was collected from diverse habitats such as bushes, road side, hillside, or grassland. Only 2 accessions of L. cernuum were collected from Fengcheng city and Fushun city, and only 3 accessions of L. concolor var. megalanthum were collected from Tieling and Jiaohe city. Therefore, the distribution of L. cernuum and L. concolor var. megalanthum was rather narrow as compared to other species. L. amabile also had narrow geographic distribution, which seemed to be concentrated in Dandong city near North Korea. The analytic hierarchy process was employed to evaluate ornamental characteristic and utilization potential of 9 collected species. It seemed that L. lancifolium and L. cernuum got the highest score Therefore, L. lancifolium and L. cernuum had an excellent exploitation potential. Among the 9 Lilium species, only L. cernuum had obvious purple flowers. Also, its population was very small. Besides, L. pumilum, L. concolor var. buschianum and L. leichtlini var. maximowiczii. got higher scores. Therefore, great importance had been continuously attached to L. lancifolium, L. cernuum, L. pumilum, L. concolor var. buschianum and L. leichtlini var. Maximowiczii. L. dauricum, L. distichum and L. concolor var. megalanthum got the lower score. However, that does not mean that they are worthless. They have a relatively high value in some certain aspects that implying that we should also pay attention to these species.
     16 morphological characteristics from 50 populations of 6 species and 3 varieties germplasm resources were researched. The results showed that the morphological characteristics were significantly different with high diversity among the wild lilies native to northeast China. The coefficient of variation were high and more than 25% except for leaf long (23.35%), of which the cofficient of variation of style length and leaf width were most highest, up to 64.57% and 59.37% respectively. The morphological diversity was high, and the average diversity index was 1.85, of which the diversity index of leaf length and inner petal width, were highest, up to 2.88 and 2.87 respectively. In PCA analysis, the first four principal components represented 87.51% of the morphological diversity. The significant morphological divergence consisted of outer petal width, inner petal length, inner petal width, flower color, flower type, peduncle length and leaf length.Based on the morphological data, 50 wild lilies were cluster into three groups. The first group included 30 accessions with the smaller flower, L. pumilum, L. concolor var. buschianum, L. concolor var. megalanthum, L. amabile and L. cernuum, the second group included 19 accessions with large flower, L. lancifolium, L. leichtlinii var. maximowiczii and L. dauricum, and the third group included L. distichum.
     The pollen was observed by light microscope and scaning electronic microscope. The result showed that pollen exists for single grain, and the symmetry is strong. The pollen shapes of wild Lilium are boat shape in equator view and there is a ditch which extends several to the two-pole. The pollen shapes of Lilium are oval in polar view and the edge has hollow, for sprouts the ditch. There was very significant difference on polar axis, equarorial axis, P/E among Lilium species. The result from multiple comparions showed that there was very significant difference among some Lilium species, and no significant difference among other Lilium species. Also, there was no significant difference in L. amabile from different areas. and There was very significant difference in L. lancifolium and L. pumilum from different areas.The ultrastructure of pollen surface basic type observes is the network, the net keel belt-shaped, granulated, plate bead shape or is irregular, forming the polygon or the irregular mesh. The mesh size, the density of distribution and the shape characteristic have the certain difference in different species, mesh size of some species is bigger, and others is smaller. The mesh in near polar middle is obviously bigger than the ditch edge by scaning electronic microscope
     The roots were used to study the effects of the sampling time, the pretreatment chemicals, hydrolysing time and staining on the chromosome squashing. The results showed that the optimal sampling time of roots was about 8:30~9:30 am. Of the three pretreatment chemicals used,0.1% colchicine solution for 24 hours was proved to be best. Then the root-tips were fixed with Carnoy solution for 6 hours and hydrolysed with 1 mol·L-1 HCl for 5 min (8min for L. lancifolium) at 60℃and stained with modified Carbol fuchsin solution. A very good effect of chromosome squashing could be obtained with this method. The chromosome of 9 Lilium species collected was bigger, and showed the same basic chromosome number x=12 and similar karyotype features, two large metacentric chromosome pairs and ten subtelocentric or telocentric pair. L. lancifolium was triploid (2n=3x=36) and the other species were diploid (2n=2x=24). Interspecific differences was mainly the number of chromosomes of different types and their ranking position in the karyotype, followed by the difference of the number and position of the satellite. The karyotype of all the species was 3A except for L. dauricum Ker-Gaw. with 3B. The variations of chromosome number were observed in the root-tip cells of 8 species except for L. distichum, but the variation frequency was relatively low. The aneuploidy cells of 2n=2x=22,25,26 were observed in seven diploid species with the rate of 2~10%. The aneuploidy cells of 2n=3x=34,37 were observed with the rate of 9%, and the cells with haploid chromosome number(2n=x=12) had also been observed in the triploid species L. lancifolium. B-chromosome was also observed in L. dauricum; L. concolor var. buschianum, L. concolor var. megalanthum, L. pumilum and L. lancifolium. There was 1 B-chromosome in L. lancifolium, L. concolor var. buschianum and L. concolor var. megalanthum,2 B-chromosomes in L. dauricum, and 1 B and 2 B-chromosomes in L. pumilum. Especially, the occurrence frequency of B-chromosome in L. pumilum was highest, up to 10%
     The DNA polymorphism from 50 accessions of 6 species and 3 varieties in Lilium native to Northeast China was studied using randomly amplified polymorphic DNA (RAPD) markers in the experiment. A total of 105 clear and reproducible bands were generated from twelve RAPD primers, of which 86 were polymorphic, with an average of 7.2 polymorphic bands, which indicated that the 50 wild lily accessions had high level of genetic diversity. The dendrogram based on RAPD data were constructed by using UPGMA analysis. The 50 wild lilies clustered into two groups. The first group included 38 accessions involved in L. leichtlinii var. maximowiczii, L. lancifolium, L. dauricum, L. amabile, L. distichum, L. concolor var. buschianum and L. concolor var. megalanthum. The second group included 12 accessions involved in L. pumilum and L. cernuum. The first group can be divided into two subgroups. The first subgroup involved in L. leichtlinii var. maximowiczii, L. dauricum, L. amabile, and L. distichum, and the second subgroup involved in L. lancifolium, L. concolor var. buschianum and L. concolor var. megalanthum. The results showed that L. lancifolium had close genetic relationship with L. concolor var. buschianum, but distant genetic relationship with L. amabile, L. pumilum and L. cernuum of Sect Sinomartagon. The genetic relationship was close between L. pumilum and L. cernuum.
引文
1. 白锦荣,潘会堂,张启翔.2009.月季SSR-PCR反应体系的建立和优化.华北农学报,24(3):184-188.
    2. 鲍隆友,周杰,刘玉军.2004.西藏野生百合属植物资源及其开发利用.中国林副特产,2:54-55.
    3. 查振道.1992.百合引种栽培试验.林业科技通讯.7:30-32.
    4. 车飞,牛立新,张延龙,等.2008.秦巴山区野生百合资源及其生境土壤特性的调查.安徽农业科学,36(23):9955-9957.
    5. 陈丽梅,李雪.2003.兰州百合B染色体的初步研究.西北植物学报,23(11):2007-2010.
    6. 陈亮,童启庆,庄晚芳.1992.茶树花粉形态及其模糊聚类的研究.浙江农业大学学报,18(2):29-36.
    7. 陈为民,宋为民.1982.卷丹和青岛百合的组织培养及植株分化.植物生理学通报,2:35-36.
    8. 陈为民.1983.百合离体培养再生植株.植物生理学通报,3:46.
    9. 陈向明,郑国生,孟丽.2002.不同花色牡丹品种亲缘关系的RAPD-PCR分析.中国农业科学,35(5):546-555.
    10.陈志秀.1995.蜡梅17个品种过氧化物同工酶的研究.植物研究,15(3):403-411.
    11.戴小红,张延龙,,牛立新.2006.百合属4种植物的核型研究.西北植物学报,26(1):50-56.
    12.邓传良,李存胜,周坚,等.2006.长筒石蒜种质资源的ISSR研究.河南师范大学学报(自然科学版),34(1):98-101.
    13.丁一巨,赵奇僧,周本琳.1993.自然保护区观赏植物资源评价及其应用.南京林业大学学报,17(1):21-26.
    14.董燕,韩见宇,孙超.2007.百合属七种植物的引种栽培一生长发育规律研究,26(12):90-92.
    15.封培波,胡永红,张启翔.2003.上海露地宿根花卉景观价值的综合评价.北京林业大学学报,25(6):84-87.
    16.傅立国,陈潭清,郎楷永,等.2002.中国高等植物.青岛:青岛出版社.
    17.甘娜,’谭向红,陈其兵,等.2006.应用RAPD标记和细胞质基因组PCR-RFLP技术研究大花蕙兰的遗传多样性.园艺学报,33(2):349-355.
    18.高江云,陈进,夏永梅.2002.国产姜科植物观赏特性评价及优良种类筛选.园艺学报,29(2):158-162.
    19.葛颂,洪德元.1994.遗传多样性及其检测方法,见:中国科学院遗传多样性委员会编,生物多样性研究的原理和方法.北京:中国科技出版社.
    20.葛颂.1994.酶电泳资料和系统与进化植物学研究综述.武汉植物学研究,12(1):71-84.
    21.龚双军,万卉敏,杨秋生.2009.牡丹栽培品种数量分类的初步研究.江西农业学报,21(12):66-69.
    22.郭思琪,张新春,张厚良.2004.小兴安岭引种百合栽培试验.林业实用技术,4:39-40.
    23.郭先锋,王莲英,袁涛.2005.4种野生芍药的花粉形态研究.林业科学,41(5):184-188.
    24.郭先锋,王莲英.2007.部分芍药种质资源的RAPD分析.园艺学报,34(5):1321-1326.
    25.国家环境保护局主持《中国生物多样性国情研究报告》编写组编.1998.中国生物多样性国情报告.北京:中国环境科学出版社.
    26.韩凤鸣,牛立新,张延龙,等.2006.百合性状的主成分分析.西北林学院学报,21(2):90-92.
    27.郝岗平,杨清,吴忠义,等.2004.植物的单核昔酸多态性及其在作物遗传育种中的应用.植物学通报,21(5):618-624.
    28.郝海平,张金谈.1988.醋酸酐分解作用与花粉形状体积的变化.植物学报,30(6):655-663.
    29.何敬胜,李作洲,黄宏文.2005.濒危物种巴东木莲的等位酶遗传多样性及其保护策略.生物多样性,13(1):27-35.
    30.何显静,李标,周利杰,等.2003.云南5种百合形态多样性研究.黑龙江农业科学,6:6-28.
    31.何显静.2003.云南三种百合居群遗传学研究.硕士学位论文.昆明:云南大学.
    32.洪德元.1990.植物细胞分类学.北京:科学出版社.
    33.胡凤荣,刘光欣,席梦,等.2009.淡黄花百合根尖染色体C-带分析.分子植物育种,7(1):79-81.
    34.胡凤荣,刘光欣,席梦利,等.2009.药百合根尖染色体C-带分析.南京林业大学学报(自然科学版),33(3):17-19.
    35.胡凤荣,刘光欣,席梦利,等.2009.宜昌百合根尖染色体C-带分析.植物研究,29(1):12-14.
    36.胡国富,李凤兰,袁强,等.2007.四种花色一串红RAPD分析.黑龙江农业科学,5:65-67.
    37.胡守荣,扩夏铬,郭长英,等.2001.林木遗传多样性研究方法概况.东北林业大学学报,29(3):72-75.
    38.胡书能,方贤.1985.同工酶技术及其应用.长沙:湖南科学技术出版社.
    39.胡树贵,李艳.2009.44个百合品种同工酶遗传多样性研究.西部林业科学,38(4):27-35.
    40.胡薇,黄儒珠,潘晓华,等.2008.建兰38个品种的RAPD分析.园艺学报,35(2):289-294.
    41.胡延吉,赵檀方.1994.小麦农艺性状主成分分析与种质资源评价的研究.作物研究,8(2):31-34
    42.黄启堂,游水生,黄榕辉.1997.运用层次分析法评价木质藤本观赏植物资源.福建林学院学报,17(3):269-272.
    43.黄瑞复,李劲峰.1996.宝兴百合四个居群的核型及其分类研究.云南植物研究,增刊Ⅷ:15-22.
    44.黄为平,郑晓鹰.1996.同工酶电泳与田间种植方法鉴定大白菜杂交种纯度的相关研究.种子,6:16-17.
    45.贾继增.1996.分子标记种质资源鉴定和分子标记育种.中国农业科学,29(4):1-10.
    46.贾月慧,张克中,王葳蕤,等.2005.几种中国野生百合的过氧化物酶同工酶.东北林业大学学报,33(2):15-17.
    47.姜立春,彭正松.2005.B染色体的研究进展.吉林师范大学学报(自然科学版),8(3):51-54.
    48.蒋彩虹,王元英,:孙玉合.2007.SSR和ISSR标记技术应用进展.中国烟草科学, 28(2):1-5.
    49.雷家军,庞兰,林翼飞,关婧竹.2009.卷丹百合种间杂交种胚培养研究.沈阳农业大学学报,40(1):84-87.
    50.黎海利,董丽.2009.萱草部分野生种和栽培品种亲缘关系的AFLP分析.园艺学报,36(8):1203-1208.
    51.黎中宝,林鹏.2001.等位酶技术在植物中的应用.集美大学报(自然科学版),6(1):81-86.
    52.李保印.2007.中原牡丹品种遗传多样性及核心种质构建研究.博士毕业论文.北京:北京林业大学
    53.李国珍.1985.染色体及其研究方法.北京:科学出版社.
    54.李建平,朱霖,张立,等.1995.山茶属花粉细胞光镜与电镜结构观察.安徽农业大学学报,22(增刊):202-205.
    55.李景奇,秦小平,王聚瀛.1993.几种百合的花粉形态研究.武汉植物学研究,11(2):120-124.
    56.李懋学,陈瑞阳.1985.关于植物核型的标准化问题.武汉植物研究,3(4):297-302.
    57.李懋学,张赞平. 1996.作物染色体及其研究技术.北京:中国农业出版社.
    58.李梅春.2004.基于层次权重分析技术的垂直绿化植物资源优选.武汉理工大学学报,26(3):165-]67.
    59.李萍,石金磊,胡永红,等.2007.凤梨亚科光萼荷属与其近源属亲缘关系的ISSR分子鉴定.种子,26(11):35-40.
    60.李书心.1988.辽宁植物志.沈阳:辽宁科学技术出版社.
    61.李晓玲,独军.2008.小陇山林区野生百合属植物资源开发利用研究.甘肃科技,24(9):169-171.
    62.李雪,文婕英,曾小英,等.2005.百合属几种植物亲缘关系的可溶性蛋白质和过氧化物酶分析.西北师范大学学报(自然科学版),41(6):58-61.
    63.李云侠,魏一江,吴淑芳.2001.几种百合引种的研究.贵州科学,19,(3):39-42.
    64.梁红健,李文彬.1996.中国部分兰花品种RAPD分析.园艺学报,23(4):265-370.
    65.梁顺祥,郭洋楠,唐道城,等.2009.孔雀草POD同工酶及主要观赏性状研究.北方园艺,9:65-67.
    66.梁顺祥,唐道城,郭京,等.2007.万寿菊雄性不育品系POD同工酶及主要观赏性状的研究.北方园艺,5:201-202.
    67.梁松筠,张无休.1984.百合属中的四合花粉兼论玫红百合的分类问题.植物分类学报,22(4):297-300.
    68.梁松筠.1995.百合科(狭义)植物的分布区对中国植物区系研究的意义.植物分类学报,33(1):27-51.
    69.梁万军,王宪成,周轸世,等.1998.吉林省主要造林树种生态因子层次分析.吉林林业科技,5:13-37.
    70.林茂祥,刘正宇,任明波,等.2009.金佛山野生百合属植物资源及开发利用.中国农学通报,25(14):201-203
    71.刘光欣,胡凤荣,席梦利,等.2007.三个卷瓣组百合的根尖染色体C-带比较.分子植物育种,5(6):88-889.
    72.刘光欣,胡凤荣,席梦利,等.2008.百合根尖染色体C-带分析.江苏农业科学,6:151-152.
    73.刘光欣,胡凤荣,席梦利,等.2008.岷江百合根尖染色体的C-分带和FISH分析.分子植物育种,6(1):95-99.
    74.刘海星.2009.新疆弯刺蔷薇资源调查及遗传多样性分析.硕士毕业论文.北京:中国农业科学院.
    75.刘萍,芦锰.2009.7种不同花色35个牡丹品种遗传多样性的AFLP分析.河南中医学院学报,24(3):30-32.
    76.刘伟,周厚高,和兆荣.2009.十八个麝香百合基因型遗传差异性的RAPD分析.北方园艺,11:181-184.
    77.刘玉莲,殷学波.1996.樱花品种园艺学性状的综合评价.江苏农学院学报,17(2):39-43.
    78.龙雅宜,张金政,张兰年.1999.百合——球根花卉之王.北京:金盾出版社.
    79.龙雅宜,张金政.1998.百合属植物资源的保护与利用.植物资源与环境,(1):40-44.
    80.吕书年,赵鹂.2001.百合属植物资源的保护与利用.丽水师范专科校学报,23(5):35-37.
    81.罗建让,牛立新,张延龙,等.2006.百合野生种及品种交配亲和性的研究.西北农业学报,15(2):112-116.
    82.罗晓莹,庄雪影,杨跃生.2007.杜鹃红山茶遗传多样性的ISSR分析.热带亚热带植物学报,15(2):93-100.
    83.罗远华,莫饶,蔡林宏,等.2009.文心兰品种变异RAPD分子检测技术的建立及应用.热带农业科学,29(7):28-32.
    84.罗远华,余志金,莫光武,等.2009.石斛兰品种遗传变异的RAPD检测.安徽农业科学,37(25):11889-11891.
    85.雒新艳,戴思兰.2009.ISSR分子标记在观赏植物研究中的应用.湖北农业科学,48(7):1760-1765.
    86.马吉龙,李艳君.2000.凤凰百合—百合属一新种.武汉植物研究,18(2):115-116.
    87.马克平.1993.试论生物多样性的概念.生物多样性,1(1):22.
    88.马育华.1979.田间试验和统计方法.北京:农业出版社.
    89.毛钧,张明宇,虞泓.2003.泸定百合普洱居群遗传与变异研究.云南大学学报(自然科学版), 25(增刊):91-96.
    90.缪恒彬,陈发棣,赵宏波.2007.85个大菊品种遗传关系的ISSR分析.园艺学报,34(5):1243-1248.
    91.穆鼎.2005.观赏百合一生理、栽培、种球生产与育种.北京:中国农业出版社.
    92.彭隆金,王心农.1986.四川百合一新种.云南植物研究,8:225-226.
    93.彭隆金.1985.百合属一新种—松叶百合.云南植物研究,7(3):317-318.
    94.彭隆金.2001.百合资源与栽培.昆明:云南民族出版社.
    95.戚晓利,徐秀芳,王维人.2003.蒲公英过氧化物酶(POD)同工酶的测定.中国野生植物资源,22(2):42-43.
    96.钱虹妹,杨学军,余洪波,等.2006.应用AHP法综合评价中国百合野生种资源.江苏农业科学,4:169-172.
    97.任旭琴.2001.利用RAPD分子标记对红皮云杉种源遗传多样性的研究.硕士学位论文.哈尔滨:东北林业大学.
    98.阮晓赛,林新春,娄永峰.2008.毛竹种源遗传多样性的AFLP和ISSR分析.浙江林业科技,28(2):29-33.
    99.桑涛,徐丙声.1993.分子系统学当前的理论和方法概述及华东地区山胡椒属十二个种的分支系统学研究.植物分类学报,34(1)12-28.
    100.尚占环,姚爱兴.2002.生物遗传多样性研究方法及其保护措施.宁夏农学院学报,23(1):66-69.
    101.沈德绪主编.1998.果树育种学.北京:中国农业出版社.
    102.沈镝,方智远,戚春章,等.2009.西双版纳黄瓜群体遗传多样性的SSR分析.园艺学报,36(10):1457-1464.
    103.沈浩,刘登义.2001.遗传多样性概述.生物学杂志,18(3):5-8.
    104.沈联德.1991.药用植物学.北京:人民卫生出版社.
    105.沈振国,刘友良.1998.重金属超量积累植物研究进展.植物生理学通讯,34(2):133-139.
    106.孙启时,石猛,付沛云.1989.东北百合属植物的研究.植物研究,9(3):133-148.
    107.唐东芹,张思平,高本年.1998.用AHP法对桂花品种应用的综合评价.江苏林业科技,25(1):11-16.
    108.唐开学,邱显钦,张颢.2008.云南蔷薇属部分种质资源的SSR遗传多样性研究.园艺学报,35(8):1227-1232.
    109.田兴军.2005.生物多样性及其保护生物学.北京:化学工业出版社.
    110.田赟,雒新艳,戴思兰.2008.菊花芽变和相似品种的RAPD分析.分子植物育种,6(6):1223-1232.
    111.铁军,金山,白海艳,等.2005.芦荟属植物种间杂交及其F1代POD同工酶鉴定.广西植物,25(5):449-452.
    112.图力古尔,包海鹰,张恕茗,等.1997.乌头属植物花粉形态及其分类学意义.吉林农业大学学报,19(1):59-64.
    113.图力古尔,刘立波.1996.吉林省产5种百合的核型研究.武汉植物学研究,14(1):6-12.
    114.汪发缵,唐进,梁松筠.1986.中国百合科植物研究.云南植物研究,12(8):51-52.
    115.王丹菲,赵珺,雷家军.2006:百合种间杂交亲和性的研究.沈阳农业大学学报,37(1):26-30.
    116.王红霞,王文锋.2008.岷江百合的形态多样性研究.安徽农业科学,36(16):6762-6763.
    117.王红霞,杨保胜.2003.岷江百合居群核型变异研究.河南职业技术师范学院学报,31(3):40-44.
    118.王红霞,杨保胜.2005.通江百合形态变异式样研究.河南科技学院学报(自然科学版),25(3):8-10.
    119.王开发,王宪曾.1983.孢粉学概论.北京:北京大学出版社.
    120.王奎玲,刘庆华,刘庆超,等.2008.青岛百合杂交育种研究.中国园艺学会观赏园艺专业委员2008年学术年会.
    121.王述民,曹永生,Redden R J,等.2002.我国小豆种质资源形态多样性的鉴定和分类研究.作物学报,28(6):727-733.
    122.王玉元.1997.染色体遗传中的一个不解之谜——B染色体.武汉植物学研究,15(1):73-79.
    123.王中仁.1996.植物等位酶分析.北京:科学出版社.
    124.魏邦龙.1997.应用层次分析法AHP确定农业科研项目评估指标的权重.甘肃科学学报,9(3):70-73.
    125.魏开发,林水英,刘逸萍,等.2009.矮牵牛花瓣等位酶体系建立及几个品种亲缘关系分析.漳州师范学院学报(自然科学版),1:76-79.
    126.吴丽华.2003.室内观叶植物价值评价体系研究.福建林业科技,30(4):61-64.
    127.吴学尉,李树发,熊丽,等.2006.云南野生百合资源分布现状及保护利用.植物遗传资源学,7(3):327-330.
    128.吴振兴,王慧中,施农农.2008.兰属(Cymbidium)植物ISSR遗传多样性分析.遗传,30(5):627-632.
    129.吴祝华.2008.百合属部分种亲缘关系与岷江百合群体遗传结构研究.博士学位论文.南京:南京林业大学.
    130.向地英,张延龙,郝瑞杰,等.2006.秦巴山区及毗邻地区野生百合性状描述.中国农学通报,22(10):97-100.
    131.肖尊安.2005.植物生物技术.北京:化学工业出版社.
    132.徐丽萍,唐道城,何瑞军.2009.不同授粉方式对青海细叶百合与亚洲百合杂交结实研究.北方园艺,1:175-177.
    133.许凤,李凌,邱显钦,等.2009.云南39个野生蔷薇种间遗传多样性的SSR分析.西南大学学报 (自然科学版),3](6):83-87.
    134.许介眉.1985.四川百合科新种.植物分类学报,23:232-235.
    135.许介眉.1986.四川百合科二新种.植物研究,6(2):67-70.
    136.杨春澍,曾万章.1994.药用植物学.上海:科学技术出版社.
    137.杨利平,丁冰,刘香环.1996.东北百合属植物的细胞遗传多样性.东北林业大学学报,9(5):19-23.
    138.杨利平,刘桂芳,张彦妮.2003.百合抗性品系的培育.东北林业大学学报,31(6):33-35.
    139.杨守志,刘丰权,王秀艳.2000.几种野生百合的引种栽培.北方园艺,3:31-32.
    140.杨学明,裔传灯.2004.植物染色体原位杂交技术及其在稻属研究中的应用.植物遗传资源学报,5(4):401-405.
    141.杨玉玲,马祥庆,张木清.2006.ISSR分子标记及其在树木遗传育种研究中的应用.亚热带农业研究,2(1):18-24.
    142.姚青菊,夏冰,彭峰,等.2006.岷江流域王百合和通江百合多酚氧化酶同功酶的研究.广西植物,26(1):92-96.
    143.于守超,丰震,赵兰勇.2005.平阴玫瑰品种数量分类研究的探讨.园艺学报,32(2):327-330.
    144.虞泓,黄瑞复.1996.川百合种内核型多样性研究.云南植物研究(增刊),8:1-14.
    145.虞泓,王红霞,游丹.2000.泸定百合居群染色体形态研究.云南大学学报(自然科学版),22(1):60-67.
    146.岳玲,雷家军,王欣.2006.辽宁的4种野生百合(Lilium)的核型研究.辽宁农业科学,4:5-10.
    147.张德强,张志毅,杨凯.2000.AFLP技术在林木遗传改良中的应用.北京林业大学学报,22(6):75-78.
    148.张定成,邵建章.1991.安徽百合科二新种.植物分类学报,29(5):474-476.
    149.张海平,房伟民,陈发棣,等.2009.部分睡莲属植物形态性状的多样性分析.南京农业大学学报,32(4):47-52.
    150.张教方,于海滨,张显国,等.1994.毛百合繁殖生物学研究(Ⅲ)—毛百合种子萌发特征.东北林业大学学报,22(2):46-49.
    151.张靖国,胡红菊,徐育海,等.2009.部分湖北海棠种质的鉴定及亲缘关系分析.华中农业大学学报,28(6):736'-740.
    152.张克中,贾月慧,张启翔,等.2008.部分中国野生百合亲缘关系的AFLP技术分析.东北林业大学学报,36(2):]9-22.
    153.张丽霞,施兆鹏,王日为,等.1998.茉莉花酯酶同工酶的研究.湖南农业大学学报,24(1):18-22.
    154.张敏,黄苏珍,仇硕.2007.鸢尾属植物遗传多样性的RAPD和ISSR分析.植物资源与环境学报,16(2):6-11.
    155.张绍斌.2002.云南淡黄花百合遗传多样性与进化研究.硕士学位论文.成都:四川大学.
    156.张述景,智利红,焦乐勤等.2008.豫西山区野生百合形态特征的研究.安徽农业科学,36(16):6760-6761,6800.
    157.张西丽,周厚高,周焱,等.2000.几个百合品种花粉电镜观察及其亲缘关系分析.广西农业生物科学,19(3):175-179.
    158.张献龙,唐克轩.2004.植物生物技术.北京:科学出版社.
    159.张新春,郭思琪,刘春波.2005.百合引种栽培试验.中国林副特产,13:27-28.
    160.张玄兵,何超伟,梁带喜,等.2004.观赏竹芋的过氧化物酶同工酶研究.福建热作科技,29(1):5-7.
    161.赵冰,雒新艳,张启翔.2007.蜡梅品种的数量分类研究.园艺学报,34(4):947-954.
    162.赵东欣,赵文杰,卢奎.2008.玉兰属20种植物过氧化物同工酶研究.河南师范大学学报(自然科学版),36(5):139-142.
    163.赵焕臣,许树柏.1986.层次分析法.北京:科学出版社.
    164.赵谦,杜虹,庄东红.2008.14个蝴蝶兰品种遗传关系的ISSR分析.植物研究,28(2):227-231.
    165.赵庆芳,马世荣,曾小英,等.2005.百合栽培品种资源的RAPD分析.兰州大学学报(自然科学版),41(2):30-33.
    166.赵天榜,陈志秀,傅大立,等.1994.河南木兰属9种植物过氧化物同工酶分析.生物数学学报,9(3):84-92.
    167.赵天田,沈红香,姚允聪,等.2010.苹果属观赏海棠实生单株亲本的AFLP鉴定.园艺学报,37(1):121-128.
    168.赵祥云,陈新露,方海,等.1995.用RAPD标记评价百合品种间遗传关系.北京农学院学报,10(2):58-63.
    169.赵祥云,陈新露.1994.中国野生种质资源及其研究利用.海峡两岸花卉发展交流研讨会论文精选.北京:中国农业出版社.
    170.赵祥云,王树栋,陈新露,等.2000.百合.北京:中国农业出版社.
    171.郑成木.2003.植物分子标记原理与方法.长沙:湖南科学技术出版社.
    172.中科院植物研究所主编.1976.中国高等植物图鉴.北京:科学出版社.
    173.周朝泓.1997.三种百合植物再生植株的染色体数量变异.林业科学研究,10(6):663-667.
    174.周厚高,张西丽.1999..几种百合品种遗传亲缘关系的等位酶分析.西南农业大学学报,12(4):92-95.
    175.周兰英,王永清,张丽,等.2009.46种杜鹃花属植物表型性状的数量分类.林业科学,45(8):67-75.
    176.周守标,余本祺,罗琦,等.2005.石蒜属植物花粉形态及分类研究,园艺学报,32(5):9-14.
    177.周延清.2005.DNA分子标记技术在植物研究中的应用.北京:化学工业出版社.
    178.周鹞.2002.长白山百合属植物野生资源及其开发利用.中国野生资源,21(3):22-23.
    179.周以良主编.1985.黑龙江省植物志.哈尔滨:东北林业大学出版社.
    180.周志林,聂以春,张献龙,等.2008.棉花体细胞培养中染色体的变异.江苏农业学报,24(2):126-129.
    181.朱根发,李冬梅,.郭振飞.2009.中国墨兰品种遗传多样性的AFLP分析.中山大学学报(自然科学版),48(3):69-73.
    182.朱朋波,赵统利,李玉娟,等.2006.江苏云台山野生百合种质资源调查.江苏农业科学,1:144-145.
    183.祝正银.1993.峨眉山百合属一新种.植物研究,13:54-55.
    184.邹春静,盛晓峰,韩文卿,等.2003.同工酶分析技术及其在植物研究中的应用.生态学杂志,22(6):63-69.
    185.邹喻苹,葛颂,王晓东.2001.系统与进化植物学中的分子标记.北京:科学出版社.
    186.左志锐,穆鼎,高俊平,等.2005.百合遗传多样及亲缘关系的RAPD分析.园艺学报,32(3):468-472.
    187. Ando T, Kurata M, Sasaki S, et al.1995. Comparative morphological studies on infraspecific taxa of Petunia integrifolia (Hook.) Schinz et Thell (Solanaceae). Jouranl of Japan Botany,70 (4):205-217.
    188. Baker A J M.19,81. Accumulators and excluders:Stradegies in response of plants to heavy metals. Journal of Plant Nutrition,3:643-654.
    189. Ballard R, Rajapakse S, Abbott A, et al.1996. DNA markers in roses and their use for cultivar identification and genome mapping. Acta Horticulturae,424:265-268.
    190. Barracosa P, Lima M B, Cravador A.2008. Analysis of genetic diversity in Portuguese Ceratonia siliqua L. cultivars using RAPD and AFLP markers. Scientia Horticulturae,118:189-199.
    191. Beukeboom L W.1994. Bewildering Bs:an impression of the 1st B-chromosome conference. Heredity, 73:328-336.
    192. Bornet B, Branchard M.2001. Nonanchored inter simple sequence repeat(ISSR)markers: Reproductible and specifictools for genome fingerprinting. Plant Molecular Biology Reporter,19: 209-210.
    193. Boronnikova S V, Kokaeva Z G, Gostimsky S A, et al.2007. Analysis of DNA polymorphism in a relict Uralian species, large-flowered foxglove (Digitalis grandiflora Mill.) using RAPD and ISSR markers. Russian Journal of Genetics,43(5):530-535.
    194. Brooks R R, Shaw S, Marfil A A.1981. The chemical form and physiological function of nickel in some Iberian alyssum species. Physiologia Plantarum,51:161-170.
    195. Caetano A G.1995. DNA amplification finger printing analysis of Bermuda grass:Genetic relationship between species and inter-specific crosses. Theoretical and Applied Genetics,91(2):228-235
    196. Choi S H, Kim M J, Lee J S, et al.2006. Genetic diversity and phylogenetic relationships among and within species of oriental Cymbidiums based on RAPD analysis. Scientia Horticulturae,108:79-85.
    197.Danilo A, Claudio M, Rodrigo I.2006. Genetic diversity of wild species and cultivated varieties of alstroemeria estimated through morphological descriptors and RAPD markers. Scientia Horticulturae, 108:86-90.
    198. Dey S S., Singh A K, Chandel D.et al.2006. Genetic diversity of bitter gourd(Momordica charantia L.) genotypes revealed by RAPD markers and agronomic traits. Scientia Horticulturae,109:21-28.
    199. Diwan N, Mclntosh M S, Bauehan G R.1995. Methods of developing a core collection of annual Medicago speeies. Theoretical and Applied Genetics,90:755-761.
    200. Donoghue M J, Sanderson M J.1992. The suitability of molecular and morphological evidence in reconstructing. plant phylogeny. In Soltis D S, Soltis D. E., and Doyle J. J, Eds, Molecular plant systematic. NewYork:Champan and Hall.
    201. Ebrahimi R, Zamani Z, Kashi A.2009. Genetic diversity evaluation of wild Persian shallot(Allium hirtifolium Boiss.) using morphological and RAPD markers. Scientia Horticulturae,119:345-351
    202. Erdtman G.1969. Handbook of palynology, morphology taxonomy-Ecology. Copenhagen: Munksgaard.
    203. Evans K M, Newbigin E, Ladiges P Y.2002. An investigation of genetic variation in Banksia integrifolia (Proteaceae) by the use of the AFLP technique. Australian Systematic Botany,15 (1): 9-17.
    204. Fang D Q, Roose M L.1997. Identification of closely related citrus cultivars with inter-simple sequence repeat markers. Theoretical and Applied Genetics,95:408-417.
    205. Fu X P, Ning G G, Gao L P, et al.2008. Genetic diversity of Dianthus accessions as assessed using two molecular marker systems (SRAPs and ISSRs) and morphological traits. Scientia Horticulturae,117: 263-270
    206. Goulao L, Monte-Corvo L, Oliveira C M.2008. Phenetic characterization of plum cultivars by highmultiplex ratiomarkers:amplified fragment length polymorphisms and inter-simple sequence repeats. Journal of the American Society for Horticultural Science,126 (1):72-77.
    207. Hamriek J L, Godt M J W.1989. Allozyme diversity in plant species. In:Brown A.H.D., Clegg M.T., Kahler A.L., et al. Plant population genetics, breeding and genetic resources. Sinauer Associates Inc, Sunderland, Massachusetts, USA:43-63.
    208. Harris H.1966. Enzyme polymorphism in man. Proceedings of the Royal Society of London Series B-biological Sciences,164:298-310
    209. Haw S G.1986. The taxonomy of Chinese lilies. In:The lilies of China. Portland:Timber press.
    210. Huang J C, Tanabe K, Itai A.2003. Identification of flowering lotus cultivars by ISSR (inter-simple sequence repeat) markers. Horticultural Research (Japan),2(4):259-264.
    211. YANG J, ZHANG S, LIU J. et al.2009. Genetic diversity of the endangered species Rosa rugosa Thunb. in China and implications for conservation strategies. Journal of Systematics and Evolution, 47(6):515-524.
    212. Keil G, Griffin A R.1994. Use of random amplified polymorphic DNA (RAPD) markers in the discrimination and verification of genotypes in Eucalyptus. Theoretical and Applied Genetics,89: 442-450.
    213. Kim S H, Huh M K, Lee J H.2007. Genetic relationships of among taxa of genus Sorbus based on ISSR marker analysis. Miskininkyste,1(61):69-75.
    214. Labra M, Grassi F, Bardini M, et al 2003. Genetic relationships in Opuntia Mill genus (Cactaceae) detected by molecular marker. Plant Science,165 (5):1129-1136.
    215. Lee W B, Choi S Y, KimY S.1993. An application of random amplified polymorphic DNA (RAPD) to syste matics of some species of Lilium in Korea. Korean Journal of Plant Taxonomy,23(2):35-42.
    216. Levan A, Fredga K, Sandberg A A.1964. Nomenclature for centromeric position on chromosomes. Hereditas,52:201-220.
    217. Li F G, Gan S M, Weng Q J, et al.2008. RAPD and morphological diversity among four populations of the tropical tree species Paramichelia baillonii (Pierre) Hu in China. Forest Ecology and Management,255:1793-1801.
    218. Lu J, Knox M R, Amborse M J, et al.1996. Comparative analysis of genetic diversity in pea assessed by RFLP and PCR-based methods. Theoretical and Applied Genetics,93:1103-1111.
    219.. Malgas R R, Potts A J., Oettle N M. et al.2010. Distribution, quantitative morphological variation and preliminary molecular analysis of different growth forms of wild rooibos(Aspalathus linearis) in the northern Cederberg and on the Bokkeveld Plateau. South African Journal of Botany,76:72-81.
    220. Martin C, Uberhuaga E, Perez C.2002. Application of RAPD markers in the characterization of Chrysanthemum variaties and the assessment of somaclonal vatiation. Euphytica,127:247-253.
    221. Merrel D J.1981. Ecological genetics. London. Minneapolis:University of Minnesota Press.
    222. Meyer W, Mitchell T G, Mitchell E Z, et al.1993. Hybridization probes for conventional DNA fingerprinting used as single primers in the polymerase chain reaction to distinguish strains of Cryptococcus neoformans. Journal of Clinical Microbiology,31(9):2274-2280.
    223. Michikazu H, Kaori I, Hiroshi O, et al.2001. Biogeography and origin of Lilium longiflorum and L. formosanum (Liliaceae) endemic to the Ryukyu Archipelago and Taiwan determined by allozyme diversity. American Journal of Botany,88(7):1230-1239.
    224. Moja S, Univ J M.2002. Hybridization in the section Mentha (Lamiaceae) inferred from AFLP markers. American Journal of Botany,89 (12):2017-2023.
    225. Muisers J J M, Van O J C, Vna T J M, et al.1995. Molecular markers as a tool for breeding for flower longevity in Asiatic Hybrid lilies. Acta Horticulturae,420:68-71
    226. Noyer JL, Causse S, TomekpeK, et al.2005. A new image of plantain diversity assessed by SSR, AFLP and MSAP marker. Genetica,124:61-69.
    227. Ohara T, WakoT, NunomeT, et al.2005. Relationship between heterosis and genetic distances as revealed by AFLP markers in inter-varietal F1 hybrids of bunching onion (Allium fistulosum). Journal of the Japanese Society for Horticultural Science,74 (1):68-77.
    228. Persson H A, Lundquist K, Nybom H.1998. RAPD analysis of genetic variation within and among populations of Turk's caplily (Lilium martagon L.). Hereditas,128(3):213-220
    229. Poncet C, Bonnet G, Pionnat S, et al.2001. Spread of crown gall disea in rose cultures. Acta Horticulturae,547:75-81.
    230. Raccuia S.A., Mainolfi A., Mandolino G., et al.2004. Genetic diversity in Cynara cardunculus revealed by AFLP markers:Comparison between cultivars and wild types from Sicily. Plant Breeding, 123 (3):280-284.
    231. Ratnaparkhe M B, Tekeoglu M, Muehlbauer F J.1998. Inter-simple-sequence-repeat (SSR) polymorphisms are useful for finding markers associated with disease resistance gene clusters. Theoretical and Applied Genetics,97(4):515-519.
    232. Rieger R, Michaelis A, Green M M.1991. Glossary of geneetics fifth edition. Springer Verlga, German,209:89-90
    233. Robinson N J., Tommey A M.1993. Plant metallothioneins. Biochemical Journal,295:1-10.
    234. Rout G R, Senapati S K, Aparajita S.2007. Studies on the genetic relationship among 13 cultivars of Calathea (Marantaceae) using RAPD and ISSR markers. Advances in Horticultural Science,21(3): 147-155.
    235. Salimath S S, Deolivieri A C, Godmin I D, et al.1995. Assessment of genome origins and genetic diversity in the genus Eleusine with DNA markers. Genome,38:757-763.
    236. Satty T L.1980. The analytic hierachy process. New York:McGraw Hill.
    237. Schaal B A, Leverich W J, Rogstad S H.1991. Comparison of methods for assessing genetic variation in plant conservation biology. In Falk D.A. and K.E. Holsinger (eds.):Genetics and conservation of rare plants. New York:Oxford University Press.
    238. Solouki M, Mehdikhani H, Zeinali H, et al.2008. Study of genetic diversity in Chamomile (Matricaria chamomilla) based on morphological traits and molecular markers. Scientia Horticulturae, 117:281-287.
    239. Stebbines G L.1950. Artifical and natural hybrid in the Gramineae, tribe Hordeae IV. Two triploid hybrids of Agropyron and Elynus. American Journal of Botany,37:338-392.
    240. Stebbins G L.1971. Chromosomal evolution in higher plant. London:Edward Arnold Limited.
    241. Sun G L, Salomon B, Bothmer R V.2002. Microsatellite polymorphism and genetic diffrentiation in three Norwegian populations of Elymus alaskamus (Poaceae). Plant Systematics and Evolution,234: 101-112.
    242. Syamkumar S, Sasikumar B.2007. Molecular marker based genetic diversity analysis of Curcuma species from India. Scientia Horticulturae,112:235-241.
    243. Talhinhas P, Nevesmartins J, Leitao J.2002. Inter-and intra-specific genetic diversity in Lupinus evaluated with AFLP, ISSR and RAPD markers. Wild and cultivatedlupins from the tropics to the poles:Proceedings of the 10th international lupin conference. Laugarvatn, Iceland,6:19-24.
    244. Terzopoulos P J, Bebeli P J.2008. DNA and morphological diversity of selected Greek tomato (Solarium lycopersicum L.) landraces. Scientia Horticulturae,116:354-361.
    245. Thimmappaiah, Santhosh W G, Shobha D, et al.2009. Assessment of genetic diversity in cashew germplasm using RAPD and ISSR markers. Scientia Horticulturae,120:411-417.
    246. Tomotaro N, Keiichi O, Tae U, et al.1999. A molecular phylogeny of Lilium in the internal transcribed spacer region of nuclear ribosomal DNA. Journal of Molecular Evolution,49:238-249.
    247. Van de Kasteele F S C S.1974. Conservation of wild Lilium species. Biological Conservation,6(1): 26-31.
    248. Virk P S, Zhu J, Newbury H J, et al.2000. Effectiveness of different classes of molecular marker for classifying and revealing variation in rice (Oryza sativa) germplasm. Euphytica,112(3):275-284.
    249.Walker J W.原始被子植物花粉外壁进化的意义.中科院植物所古植物研究室孢粉组译.1980.北京:科学出版社.
    250. Wang G Z, MatsuokaY, Tsunewaki K.2000. Evolutionary features of chondriome divergence in Triticum (wheat) and Aegilopsshown by RFLP analysis of mitochondrial DNAs. Theoretical and Applied Genetics,100:221-231
    251. Wang J Y, Chuang K C, Fan M J.2001. Comparative analysis of genetic similarity among Anthurium cultivars by using ISSR and RAPD markers. Journal of Agricultural Research of China,50(1):54-67.
    252. Williams J G K, Kubelik A R, Livak K J, et al.1990.18 DNA polymorphisms amplified by arbitrary primers are useful as genetic markers. Nucleic Acidres:6531-6534.
    253. Wodehouse R P.1935. Pollen Grains. New York:Mc Graw Hil Book Co. Inc.
    254. Wu K, Jones R, Dannaeberger L, et al.1994. Detection of microsatellite polymorphisms without cloning. Nucleic Acids Research,22(15):3257-3258.
    255. Yamagishi M.1995. Detection of section-specific random amplifies polymorphic DNA (RAPD) markers in Lilium. Theoretical and Applied Genetics,91(6/7):830-835
    256. Yang J H, Zhang S P, Liu J. et al.2009. Genetic diversity of the endangered species Rosa rugosa Thunb. In China and implications for conservation strategies. Journal of Systematics and Evolution, 47(6):515-524.
    257. Yan Z, Denneboom C, Hattendorf A, et al.2005. Construction of an integrated map of rose with AFLP, SSR, PK, RGA, RFLP, SCAR and morphological markers. Theoretical and Applied Genetics,110: 766-777.
    258. Zhang J, Burgos N R, Ma K.et al.2008. Genetic diversity and relationship of weedy rice in Taizhou City, Jiangsu Province, China. Rice Science,15(4):295-302.
    259. Zietkiewic Z E, Rahh A, Labuda D,1994. Genome fingerprinting by simple sequence repeat (SSR)-anchored polymerase chain reaction amplification. Genomics,20(2):176-183.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700