[1]Lu B R. Taxonomy of the genus Oryza (Poaceae): A historical perspective and current status. Int Rice Res Notes, 1999, 24: 4-8.
[2]Aggarwal R K, Brar D S, Khush G S. Two new genomes in the Oryza complex identified on the basic of molecular divergence analysis using total genomic DNA hybridization. Mol Gen Genet, 1997, 254: 1-12.
[3]Vaughan D A. The genus Oryza L. Current status of taxonomy. IRRI Research Paper Series No. 138. Manila: IRRI, 1989: 1-21.
[4]Vaughan D A, Morishima H, Kadowaki K. Diversity in the Oryza genus. Curr Opin Plant Biol, 2003, 6: 139-146.
[5]Ge S, Sang T, Lu B R, et al. Phylogeny of rice genomes with emphasis on origins of allotetraploid species. Proc Natl Acad Sci USA, 1999, 96: 14400-14405.
[6]Liu L, Lafitte R, Guan D. Wild Oryza species as potential sources of droughtadaptive traits. Euphytica, 2004, 138: 149-161.
[7]Jena K K, Kochert G. Restriction fragment length polymorphism analysis of CCDDgenome species of the genus Oryza L. Plant Mol Biol, 1991, 16: 831-839.
[8]Gopalakrishnan R, Sampath S. Taxonomic status and the origin of American tetraploid species of the series Latifoliae Tateoka in the genus Oryza. Indian J Agric Sci, 1967, 37: 465-475.
[9]Aggarwal R K, Brar D S, Nandi S, et al. Phylogenetic relationships among Oryza species revealed by AFLP markers. Theor Appl Genet, 1999, 98: 1320-1328.
[10]Bao Y, Ge S. Identification of Oryza species with the CD genome based on RFLP analysis of nuclear ribosomal ITS sequences. Acta Bot Sin, 2003, 45(7): 762-765.
[11]Bao Y, Ge S. Origin and phylogeny of Oryza species with the CD genome based on multiplegene sequence data. Plant Syst, 2004, 249: 55-66.
[12]蓝伟侦, 覃瑞, 李刚,等. 利用C基因组C0t1 DNA比较分析稻属A, B, C, D基因组. 科学通报, 2006, 51(12): 1422-1431.
[13]Flavell R B. Repetitive DNA and chromosome evolution in plants. Philos Trans R Soc Lond B: Biol Sci, 1986, 312: 227-242.
[14]Bennetzen J L, Ma J, Devos K M. Mechanisms of recent genome size variation in flowering plants. Ann Bot, 2005, 95: 127-132.
[15]Matyasek R, Gazdova B, Fajkus J, et al. NTRS, a new family of highly repetitive DNAs specific for the T1 chromosome of tobacco. Chromosoma, 1997, 106: 369-379.
[16]Zwick M S, Hanson R E, Mcknight T D, et al. A rapid procedure for the isolation of C0t1 DNA from plants. Genome, 1997, 40: 138-142.
[17]蓝伟侦, 何光存, 吴士筠, 等. 利用水稻C0t1 DNA和基因组DNA对栽培稻、药用野生稻和疣粒野生稻基因组的比较分析.中国农业科学, 2006, 39(6): 1083-1090.
[18]Ren N, Song Y C, Bi X Z, et al.The physical location of genes cdc2 and prh1 in maize (Zea mays L.). Hereditas, 1997, 126(3): 211-217.
[19]Jiang J M, Gill B S, Wang G L, et al. Metaphase and interphase fluorescence in situ hybridization mapping of the rice genome with bacterial artificial chromosome. Proc Natl Acad Sci USA, 1995, 92: 4487-4491.
[20]Wei W H, Qin R, Song Y C, et al. Comparative analyses to diseases resistant and nonresistant lines from maize Zea diploperennis by GISH. Bot Bull Acad Sin, 2001, 42: 109-114.
[21]Cheng Z K, Dong F G, Langdon T, et al. Functional rice centromeres are marked by a satellite repeat and a centromerespecific retrotransposon. Plant Cell, 2002, 14: 1691-1704.
[22]Ren F G, Lu B R, Li S Q, et al. A comparative study of genetic relationships among the AAgenome Oryza species using RAPD and SSR markers. Theor Appl Genet, 2003, 108: 113-120.
[23]Schwarzacher T, Leitch A R, Bennett M D, et al. In situ hybridization of parental genomes in a wide hybrid. Ann Bot, 1989, 64: 315-324.
[24]Fukui K, Shishido R, Kinoshita T. Identification of the rice D genome chromosomes by genomic in situ hybridization. Theor Appl Genet, 1997, 95: 1239-1245.
[25]Li C B, Zhang D M, Ge S, et al. Differentiation and inter genomic relationships among C, E and D genomes in the Oryza officinalis complex (Poaceae) as revealed by multicolor genomic in situ hybridization. Theor Appl Genet, 2001, 103:197-203.
[26]Sakurako U, Hiroshi I, Nobuko O, et al. Repetitive sequences: Cause for variation in genome size and chromosome morphology in the genus Oryza. Plant Mol Biol, 1997, 35: 791-799.
[27]Nobuko O, Kijima K, Akiyama Y, et al. Quantification of total genomic DNA and selected repetitive sequences reveals concurrent changes in different DNA families in indica and japonica rice. Mol Gen Genet, 2000, 263: 388-394.
[28]Toshie M, Ken L N, Hiroko M, et al. Genome size of twenty wild species of Oryza determined by flow cytometric and chromosome analyses. Breeding Sci, 2007, 57: 73-78.
[29]Second G, Rouhan G. Humanmediated emergence as a weed and invasive radiation in the wild of the CD genome allotetraploid rice species (Oryza, Poaceae)in the Neotropics. PLoS ONE, 2008, 3(7): e2613. doi:10.1371/journal.pone.0002613
[30]Yin P, Hartemink A J.Theoretical and practical advances in genome halving. Bioinformatics, 2005, 21: 869-879.
[31]Yogeeswaran K, Frary A, York T L, et al. Comparative genome analyses of Arabidopsis spp.: Inferring chromosomal rearrangement events in the evolutionary history of A. thaliana. Genome Res, 2005, 15: 505-515.
[32]Han F, Fedak G, Guo W, et al. Rapid and repeatable elimination of a parental genomespecific DNA repeat (pGc1R1a) in newly synthesized wheat allopolyploids. Genetics, 2005, 170: 1239-1245.
[33]Ma X F, Gustafson J P. Timing and rate of genome variation in triticale following allopolyploidization. Genome, 2006, 49: 950-958.