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Tree resolution increases as data are added to the phylogenetic analysis.



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Phylogeny of the temperate bamboos based on an ML analysis



        ½üÈÕ£¬À¥Ã÷Ö²ÎïËù¿ÆÑÐÈËÔ±ÀûÓÃÒ»ÖÖ¼ò»¯»ùÒò×é²âÐòµÄ·½·¨¼´RAD (restriction-site-associated DNA) ²âÐò·½·¨£¬ÔÚÈ«»ùÒò×éˮƽ¿ª·¢´óÁ¿µÄSNPs±ê¼Ç£¬¶ÔµÚÎå·ÖÖ§£¨Phyllostachys clade£©¼°ÆäÏà¹ØÖ§Ïµ£¨Shibataea, and Arundinaria clades£©µÄϵͳ·¢Óý¹ØÏµ½øÐÐÁËÑо¿¡£»ùÓÚRAD²âÐòÊý¾ÝËù»ñµÃµÄSNP¾ØÕ󣬹¹½¨ÁËĿǰΪֹÖñÑǿƷֱæÂÊ×î¸ßµÄÒ»¿Ãϵͳ·¢ÓýÊ÷£¬²¢µÃµ½8¸öÖ÷ÒªµÄ·ÖÖ§£ºYushania + Fargesia,Chimonocalamus + Fargesia sect. Ampullares, alpine Bashania+Fargesia, Drepanostachyum + Himalayacalamus, Gaoligongshania, Sino-Japanese clade, Chimonobambusa, Ferrocalamus + Indocalamus¡£½á¹û±íÃ÷£¬»ùÓÚÒ¶ÂÌÌ寬¶ÎËùÃüÃûµÄµÚÎå·ÖÖ§£¨Phyllostachys clade£©£¬µÚËÄ£¨Shibataea clade£©¼°µÚÁù·ÖÖ§£¨Arundinaria clade£©¾ù²»Îªµ¥Ïµ¡£ÓëÒ¶ÂÌÌ寬¶ÎËùµÃµ½µÄ½á¹û²»Í¬µÄÊÇ£¬»ùÓÚRADÊý¾ÝµÄϵͳ·¢Óý¹ØÏµÓë°´ÕÕÐÎ̬ÐÔ×´µÄ´«Í³·ÖÀà½á¹û½ÏÒ»Ö¡£¾ßÓÐϸÐ͵ØÏ¾¥µÄÎïÖÖÐγÉÁËÁ½¸öµ¥Ïµ·ÖÖ§£¬Ò»Ö§ÎªÖ÷Òª·Ö²¼ÓÚ¶«Ñǵͺ£°ÎµØÇøµÄSino-Japanese clade£¬ÁíÒ»Ö§ÎªÌØÓзֲ¼ÓÚºá¶Ïɽ-ϲÂíÀ­ÑŸߺ£°ÎµØÇøµÄalpine Bashania¡£´ËÍ⣬Ñо¿¶Ô±ÈÁËÁ½ÖÖ²»Í¬SNPÉú³ÉµÄ·½·¨£¬»ùÓڲο¼ÐòÁбȶԵÄBWA-GATK·½·¨£¬ÒÔ¼°»ùÓÚde novo×é×°µÄStacks·½·¨¡£¾¡¹ÜÓдóÁ¿È±Ê§Êý¾ÝµÄ´æÔÚ£¬»ùÓÚÁ½ÖÖ·½·¨ËùµÃµ½µÄ×î´ó¾ØÕ󣬾ùÄÜ»ñµÃÍØÆË½á¹¹ÏàËÆ¼°¸ß·Ö±æÂʵÄϵͳ·¢ÓýÊ÷¡£¸ÃÑо¿¶ÔÓÚ½ÒʾδøÖñÀàµÄÆðÔ´ÓëÑÝ»¯¾ßÓпÆÑ§ÒâÒ壬¶Ô½øÒ»²½Ñо¿¸ÃÀàȺÎïÖÖ¶àÑùÐÔµÄÐγɺÍÑÝ»¯ÀúÊ·´òÏÂÁ˼áʵ»ù´¡¡£

        The temperate bamboos (tribe Arundinarieae, Poaceae) are strongly supported as monophyly in recent molecular studies, but taxonomic delineation and phylogenetic relationships within the tribe lack resolution. Here, we sampled 39 species (36 temperate bamboos and 3 outgroups) for restriction-site associated DNA sequencing (RAD-seq) with an emphasis on Phyllostachys clade and related clades. Using the largest data matrix for the bamboos to date, we were able to infer phylogenetic relationships with unparalleled resolution. The Phyllostachys, Shibataea, and Arundinaria clades defined from plastid phylogeny, were not supported as monophyletic group. However, the RAD-seq phylogeny largely agreed with the morphology-based taxonomy, with two clades having leptomorph rhizomes strongly supported as monophyletic group. We also explored two approaches, BWA-GATK (a mapping system) and Stacks (a grouping system), for differences in SNP calling and phylogeny inference. For the same level of missing data, the BWA-GATK pipeline produced much more SNPs in comparison with Stacks. Phylogenetic analyses of the largest data matrices from both pipelines, using concatenation and coalescent methods provided similar tree topologies, despite the presence of missing data. Our study demonstrates the utility of RAD-seq data for elucidating phylogenetic relationships between genera and higher taxonomic levels in this important but phylogenetically challenging group.
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