Mort Mark E., Soltis Douglas E., Soltis Pamela S., Francisco-Ortega Javier, Santos-Guerra Arnoldo
Department of Biological Sciences, Eastern Illinois University, Charleston, Illinois 61920 USA. Department of Biological Sciences, Washington State University, Pullman, Washington 99164 USA. Department of Biological Sciences, Florida International University, Miami, Florida 33199 USA. Jardin Acclimacion de La Orotava, Calle Retema, La Orotava, Tenerife, Canary Islands, Spain.
Am J Bot. 2001 Jan;88(1):76-91.
Chloroplast gene matK sequence data were used to estimate the phylogeny of 112 species of Crassulaceae sampled from 33 genera and all six recognized subfamilies. Our analyses suggest that five of six subfamilies recognized in the most recent comprehensive classification of the family are not monophyletic. Instead, we recovered a basal split in Crassulaceae between the southern African CRASSULA: clade (Crassuloideae) and the rest of the family (Sedoideae). These results are compatible with recent studies of cpDNA restriction site analyses. Within Sedoideae, four subclades were also recovered: KALANCHOE:, Leucosedum, Acre, and AEONIUM:; evidence also exists for a TELEPHIUM: clade and SEMPERVIVUM: clade. The genus SEDUM: is highly polyphyletic with representatives spread throughout the large Sedoideae clade. Sympetaly and polymerous flowers have arisen multiple times in Crassulaceae and thus are not appropriate characters upon which to base subfamilial limits, as has been done in the past. One floral character, haplostemy, appears to be confined to the well-supported CRASSULA: clade. Our analyses suggest a southern African origin of the family, with subsequent dispersal northward into the Mediterranean region. From there, the family spread to Asia/eastern Europe and northern Europe; two separate lineages of European Crassulaceae subsequently dispersed to North America and underwent substantial diversification. Our analyses also suggest that the original base chromosome number in Crassulaceae is x = 8 and that polyploidy has played an important role in seven clades. Three of these clades are exclusively polyploid (SEMPERVIVUM: clade and two subclades within the KALANCHOE: and AEONIUM: clades), whereas four (Crassula, Telephium, Leucosedum, and ACRE: clades) comprise both diploid and polyploid taxa. Polyploidy is particularly rampant and cytological evolution especially complex in the ACRE: clade.
叶绿体基因matK序列数据被用于估计从33个属以及所有6个公认亚科中采样的112种景天科植物的系统发育。我们的分析表明,在该科最新的综合分类中所认可的6个亚科中的5个并非单系类群。相反,我们在景天科中发现了一个基部类群分支,位于南非青锁龙分支(青锁龙亚科)和该科的其余部分(景天亚科)之间。这些结果与最近关于叶绿体DNA限制性位点分析的研究结果一致。在景天亚科内,还发现了四个亚分支:伽蓝菜分支、白景天分支、长生草分支和莲花掌分支;也有证据表明存在八宝分支和长生草分支。景天属是高度多系的,其代表物种分布在整个大型景天亚科分支中。合瓣花和多基数花在景天科中多次出现,因此,如同过去所做的那样,它们并非适合作为划分亚科界限的特征。一个花部特征,单中柱,似乎仅限于得到充分支持的青锁龙分支。我们的分析表明该科起源于非洲南部,随后向北扩散到地中海地区。从那里,该科传播到亚洲/东欧和北欧;欧洲景天科的两个独立谱系随后扩散到北美并经历了大量的多样化。我们的分析还表明,景天科的原始基数染色体数为x = 8,并且多倍体在7个分支中发挥了重要作用。其中三个分支完全是多倍体(长生草分支以及伽蓝菜分支和莲花掌分支内的两个亚分支),而另外四个(青锁龙分支、八宝分支、白景天分支和长生草分支)则包含二倍体和多倍体类群。多倍体在长生草分支中尤为普遍,细胞学进化也特别复杂。