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资助项目
GST, P < 0.05) were exhibited by this species. The SAMOVA revealed seven diverging groups of related chlorotypes, six of them had distinct nonoverlapping geographical ranges: one in the northeast comprising 10 populations, a second with a southeast distribution comprising 22 populations, and the remaning four groups comprising 15 populations located in the west part of the species’ range along different river valleys. The genetic clustering of populations into three regions was also supported by analysis of molecular variance, which showed that most genetic variation (82.43%) was found among these three regions. Two clusters were distinguished by both phylogenetic analysis and genealogical analysis of chlorotypes, one consisting of chlorotypes from the western region and the second consisting of those from the eastern region. Significant genetic differences between the two regions might be attributed to vicariance and restricted gene flow, and this vicariance could be explained by the physical environmental heterogeneity on each side of the Tanaka-Kaiyong Line. Following the uplift of the Tibetan Plateau, the reorganization of the major river drainages was primarily caused by river separation and capture events. These historical events could change the distribution of S. davidii from fragmented to continuous (Upper/Lower Jinshajiang and Yalongjiang/Daduhe), and from continuous to fragmented (Nujiang and Jinshajiang/Honghe). However, spatial and temporal patterns of phylogeographic divergence are strongly associated with historical disjunction rather than modern drainage connections. Moreover, the following north-south split in the eastern region and effective isolation with their genetic diversity were essentially modelled by genetic drift. The higher chlorotype richness and genetic divergence for populations in western region compared with other two regions suggests that there were multipe refugia or in situ survival of S. davidii in the Himalayan-Hengduan Mountain region. Fixation of chlorotypes in the northeastern region and near fixation in the southeastern region suggest a recent colonization of these areas. We further found that this species underwent past range expansion around 37-303 thousand years ago (kya). The southeastern populations likely experienced a demographic expansion via unidirectional gene flow along rivers, while northeastern populations underwent a more northward expansion, both from initial populations (s) (21, 22, 23) preserved on eastern refugia (Jinshajiang). This process might have been accompanied with a series of founder effects or bottlenecks making populations genetically impoverished. 3. Phylogeographic analysisbased on nuclear sequence，We sequenced the nuclear (ncpGS) region in all populations sampled, recovering 23 nuclear haplotypes. Compared to cpDNA, both NST (0.470) and GST (0.338) were relatively lower, but NST was also significantly larger than GST. 37.10% of the total variation was distributed among regions which was much lower than that shown by chlorotypes. Thus, more extensive distribution of nuclear haplotypes was exhibited across the geographical range instead of the strong population subdivision observed in chlorotypes. Similarly to the chloroplast data, we found that genetic differentiation of nDNA was positively correlated with the geographical distance, but the increase in the geographical distance between populations did not increase the genetic differentiation of nDNA as rapidly as that of cpDNA. These contrasting levels between the chloroplast and nuclear genomes of S. davidii are likely due to limited gene flow of cpDNA by seeds vs. the extensive gene flow of nDNA by wind-mediated pollen in the population history. We also determined from nuclear markers that haplotype diversity was reduced in the southeastern and northeastern regions due to the loss of rare haplotypes in western region. This reduction of gene diversity is also a signature of founder events or recent bottleneck during post-glacial colonization. However, nuclear diversity within populations remains high. This provides evidence that regionally pollen flow might be sufficiently high to blur the genetic identity of founder populations over a reasonably large spatial scale.3. Relationships among three varieties，The phylogenetic analysis identified two phylogroups of chlorotypes, corresponding to S. davidii var. davidii and var. chuansinesis. The former was distinguished by the abscence of predonminant nuclear haplotype H1 of the latter. The monophyletic group of chlorotypes in var. davidii and var. liangshanesis showed their relatively close relationship. And their genetic divergence from the third variety appears to be relative to their slight morphological difference in leaf size and the divergent environmental niche spaces they occupy. Thus, the observed differences in morphological characters between var. chuansinesis and other two varieties can be explained by the seed dispersal limitation illustrated above (as inferred by geographical separation) and by environmental heterogeneity (as inferred by precipitation or elevation) or by a combination of both. After all, the geological changes, drainage reorganization, and floristic differences following the Himalayan uplift have been suggested to affect the genetic structure of S. davidii. These results provide new insights into the phylogeographic pattern of plants in China. In addition, the unique population genetic structure found in S. davidii has provided important insights into the evolutionary history of this species. The genetic profile uncovered in this study is also critical for its conservation management. Our study has uncovered the existence of at least two ‘evolutionary significant units’ independent units within S. davidii, corresponding to var. davidii from eastern region and var. chuansinensis from western region. The conservation efforts should first focus on most western populations and on the southeastern ones exhibiting high levels of genetic diversity, while the genetically homogeneous northeastern populations located in the degraded Loess Plateau should require much greater conservation 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floritistic composition, characteristics, endemism, origin and evolution were studied on the base of literature checked, field investigation, specimens checked and previous research work. The main result are as follows: 1. Guishan Region is rich in seed-plants. The Guishan Region flora consists of 129 families and 488 genera and 1069 species of which 6 species in 5 genera and 3 families belong to Gymnosperm, 842 species in 381 genera and 100 families belong to dicotyledon, 421 species in 102 genera and 26 families belong to monocotyledon.2. Flora Composition: The floristic elements of 62.02% tropical families and 37.98% temperate one indicates that the flora of this region has a close relationship with tropical flora historically and geographically. The floristic elements of 44.68% tropical genera and 52.96% temperate one reveals dominant temperate property, which one of the typical floristic characters in subtropical mountain region; the floristic elements of 53.83% tropical species(excluding species which are endemic to china and distribute world-wide ), 46.17% temperate ones indicates that the flora is subtropical in nature. 433 species are endemic to China ,43.96% of all the species (excluding the species world-wide).Very few species (44 species endemic to China accounted for 10.16%) distribute to the North, most of which distribute only to Shanxi, Henan, Gansu Province., indicating weak feature of temperate flora of Guishan region in nature. Statistical analysis showed that indicates that the flora of this region has a close relationship with tropical flora historically and geographically, shows transitional features in flora between tropical to temperate flora.. 3. By the comparison with five adjacent limestone and non-limestone flora on the level of family and genus, we found that the flora of Guishan Region is most closely related to the flora of Shishan Mountain and Xiaobaicaoling and Wuliang Mountain all of which situate in Central Yunnan. So the flora position of Guishan Region is: Central Yunnan Plaetau Subregion, the Yunnan Plaetau Region, the Sino-Himalayan forest Subkingdom, the east Asiatic Kingdom.4. The endemic plants in Guishan Region are rich, and the flora of Guishan Region shows limestone features. 10 genera are endemic to China, 433 species are endemic to China. Among the Chineses endemic plants, 1 genes and 7 species are endemic to Guishan Region in which 1 genes(Parasiometrum) and 3 species (Begonia guishanensis, Petrocosmea guishanensis, Parasiometrum mileens) are limestone exclusive.","jscount":"1","jsurl":"/simple-search?field1=all&field=dc.date.issued.year&advanced=false&query1=%25E5%258C%25BA%25E7%25B3%25BB%25E7%2589%25B9%25E5%25BE%2581&&fq=dc.project.title_filter%3AThe%5C+floritistic%5C+composition%2C%5C+characteristics%2C%5C+endemism%2C%5C+origin%5C+and%5C+evolution%5C+were%5C+studied%5C+on%5C+the%5C+base%5C+of%5C+literature%5C+checked%2C%5C+field%5C+investigation%2C%5C+specimens%5C+checked%5C+and%5C+previous%5C+research%5C+work.%5C+The%5C+main%5C+result%5C+are%5C+as%5C+follows%5C%3A%5C+1.%5C+Guishan%5C+Region%5C+is%5C+rich%5C+in%5C+seed%5C-plants.%5C+The%5C+Guishan%5C+Region%5C+flora%5C+consists%5C+of%5C+129%5C+families%5C+and%5C+488%5C+genera%5C+and%5C+1069%5C+species%5C+of%5C+which%5C+6%5C+species%5C+in%5C+5%5C+genera%5C+and%5C+3%5C+families%5C+belong%5C+to%5C+Gymnosperm%2C%5C+842%5C+species%5C+in%5C+381%5C+genera%5C+and%5C+100%5C+families%5C+belong%5C+to%5C+dicotyledon%2C%5C+421%5C+species%5C+in%5C+102%5C+genera%5C+and%5C+26%5C+families%5C+belong%5C+to%5C+monocotyledon.2.%5C+Flora%5C+Composition%5C%3A%5C+The%5C+floristic%5C+elements%5C+of%5C+62.02%25%5C+tropical%5C+families%5C+and%5C+37.98%25%5C+temperate%5C+one%5C+indicates%5C+that%5C+the%5C+flora%5C+of%5C+this%5C+region%5C+has%5C+a%5C+close%5C+relationship%5C+with%5C+tropical%5C+flora%5C+historically%5C+and%5C+geographically.%5C+The%5C+floristic%5C+elements%5C+of%5C+44.68%25%5C+tropical%5C+genera%5C+and%5C+52.96%25%5C+temperate%5C+one%5C+reveals%5C+dominant%5C+temperate%5C+property%2C%5C+which%5C+one%5C+of%5C+the%5C+typical%5C+floristic%5C+characters%5C+in%5C+subtropical%5C+mountain%5C+region%5C%3B%5C+the%5C+floristic%5C+elements%5C+of%5C+53.83%25%5C+tropical%5C+species%5C%28excluding%5C+species%5C+which%5C+are%5C+endemic%5C+to%5C+china%5C+and%5C+distribute%5C+world%5C-wide%5C+%5C%29%2C%5C+46.17%25%5C+temperate%5C+ones%5C+indicates%5C+that%5C+the%5C+flora%5C+is%5C+subtropical%5C+in%5C+nature.%5C+433%5C+species%5C+are%5C+endemic%5C+to%5C+China%5C+%2C43.96%25%5C+of%5C+all%5C+the%5C+species%5C+%5C%28excluding%5C+the%5C+%5C+species%5C+world%5C-wide%5C%29.Very%5C+few%5C+species%5C+%5C%2844%5C+species%5C+endemic%5C+to%5C+China%5C+accounted%5C+for%5C+10.16%25%5C%29%5C+distribute%5C+to%5C+the%5C+North%2C%5C+most%5C+of%5C+which%5C+distribute%5C+only%5C+to%5C+Shanxi%2C%5C+Henan%2C%5C+Gansu%5C+Province.%2C%5C+indicating%5C+weak%5C+feature%5C+of%5C+temperate%5C+flora%5C+of%5C+Guishan%5C+region%5C+in%5C+nature.%5C+Statistical%5C+analysis%5C+showed%5C+that%5C+%5C+indicates%5C+that%5C+the%5C+flora%5C+of%5C+this%5C+region%5C+has%5C+a%5C+close%5C+relationship%5C+with%5C+tropical%5C+flora%5C+historically%5C+and%5C+geographically%2C%5C+shows%5C+transitional%5C+features%5C+in%5C+flora%5C+between%5C+tropical%5C+to%5C+temperate%5C+flora..%5C+3.%5C+By%5C+the%5C+comparison%5C+with%5C+five%5C+adjacent%5C+limestone%5C+and%5C+non%5C-limestone%5C+flora%5C+on%5C+the%5C+level%5C+of%5C+family%5C+and%5C+genus%2C%5C+we%5C+found%5C+that%5C+the%5C+flora%5C+of%5C+Guishan%5C+Region%5C+is%5C+most%5C+closely%5C+related%5C+to%5C+the%5C+flora%5C+of%5C+Shishan%5C+Mountain%5C+and%5C+Xiaobaicaoling%5C+and%5C+Wuliang%5C+Mountain%5C+all%5C+of%5C+which%5C+situate%5C+in%5C+Central%5C+Yunnan.%5C+So%5C+the%5C+flora%5C+position%5C+of%5C+Guishan%5C+Region%5C+is%5C%3A%5C+Central%5C+Yunnan%5C+Plaetau%5C+Subregion%2C%5C+the%5C+Yunnan%5C+Plaetau%5C+Region%2C%5C+the%5C+Sino%5C-Himalayan%5C+forest%5C+Subkingdom%2C%5C+the%5C+east%5C+Asiatic%5C+Kingdom.4.%5C+The%5C+endemic%5C+plants%5C+in%5C+Guishan%5C+Region%5C+are%5C+rich%2C%5C+and%5C+the%5C+flora%5C+of%5C+Guishan%5C+Region%5C+shows%5C+limestone%5C+features.%5C+10%5C+genera%5C+are%5C+endemic%5C+to%5C+China%2C%5C+433%5C+species%5C+are%5C+endemic%5C+to%5C+China.%5C+Among%5C+the%5C+Chineses%5C+endemic%5C+plants%2C%5C+1%5C+genes%5C+and%5C+7%5C+species%5C+are%5C+endemic%5C+to%5C+Guishan%5C+Region%5C+in%5C+which%5C+1%5C+genes%5C%28Parasiometrum%5C%29%5C+and%5C+3%5C+species%5C+%5C%28Begonia%5C+guishanensis%2C%5C+Petrocosmea%5C+guishanensis%2C%5C+Parasiometrum%5C+mileens%5C%29%5C+are%5C+limestone%5C+exclusive."},{"jsname":"The origin center and diversity center of the genus Ligularia were considered to be central China and Hengduan Mountains Region (HMR) of China, respectively. In this research, we studied the phylogeographic pattern of L. hodgsonii and L. tongolensis, which was distributed in the origin center and diversity center, respectively. We aimed to infer the evolutionary process of Ligularia species. 1. The phylogeography of L. hodgsonii，Here, we investigated the phylogeographic history of L. hodgsonii disjunctively distributed in China and Japan. Two hundred and eighty individuals were collected from 29 natural populations, 23 located in China and 6 in Japan. A total of 19 haplotypes were identified with the combination of three chloroplast DNA (cpDNA) sequences variations (trnQ-5’rps16, trnL-rpl32 and psbA-trnH). At the species level, a high level of haplotype diversity (Hd) and total genetic diversity (HT) was detected. However, the average intrapopulation diversity (HS) was very low. Consequently, the population differentiation(NST = 0.989, GST = 0.933 ) was pronounced with a significant phylogeographic structure (NST > GST, p < 0.01). At the regional level, Chinese and Japanese L. hodgsonii had a similar estimate of genetic diversity (China: Hd = 0.847, HT = 0.869; Japan: Hd = 0.766, HT = 0.867). Populations from China and Japan possess unique sets of haplotypes, and no haplotypes were shared between the regions. Furthermore, both the phyloegenetic and network analyses recovered the haplotypes of China and Japan as two distinct clades. Thus, we suggested the disjunct distribution of L. hodgsonii in China and Japan may present the climatic vicariant relicts of the ancient widely distributed populations. After divergence, this species within each region experienced independent evolutionary process. In China, L. hodgsonii was distributed around the Sichuan Basin. This distribution range can be divided into five regions. They were Jiajin Mountain region, E’mei Mountain region, Yunnan-Guizhou Plateau region, Wushan-Wuling Mountain region and Qinling Mountain region. Twelve haplotypes were indentified within these regions. Each region had its own specific haplotypes, which had different ancestry in the network. We deduced that Chinese L. hodgsonii might survive the LGM in multiple isolated refugia around the Sichuan Basin. In Japan, L. hodgsonii was disjunctively distributed in northern Honshu and Hokkaido. Seven haplotypes were identified within this region. However, the genetic diversity in Honshu (Hd = 0.821) was much higher than that in Hokkaido (Hd = 0.513). And all haplotypes in Hokkaido were derived from Honshu. This haplotype distribution suggested that the northern Honshu could have served as refuge in Japan. Nested clade analysis (NCA) indicated multiple forces including the vicariance and long-distance dispersal affected the disjunctive distribution among populations of L. hodgsonii in Japan.2. The phylogeography of L. tongolensis，Ligularia tongolensis was distributed along the Jinshajiang watershed, Yalongjiang watershed and Wumeng Mountain. In order to deduce the demographic history of this species, we sequenced two chloroplast DNA (cpDNA) intergenic spacers (trnQ-5’rps16, trnL-rpl32) in 140 individuals from 14 populations of three groups (Jinshajiang vs. Yalongjiang vs. Wumeng) within this species range. High levels of haplotype diversity (Hd = 0.814) and total genetic diversity (HT = 0.862) were detected at the species level, based on a total oftwelve haplotypes identified. However, the intrapopulation diversity (HS = 0.349) was low, which led to the high levels of genetic divergence (GST = 0.595, NST = 0.614, FST = 0.597). In consideration of the speciation of L. tongolensis resulting from the uplifts of the Qinghai-Tibetan Plateau (QTP), we thought the present genetic structure of L. tongolensis was shaped by the fragmentation of ancestral populations during the courses of QTP uplifts. This was further supported by the absence of IBD tests (r = –0.291, p = 0.964), which suggest that the differentiation had not occurred in accordance with the isolation by distance model. The genetic differentiation in L. tongolensis appears to be associated with historical events. Meanwhile, H2 and H5, the dominant haplotypes that located on internal nodes and deviated from extinct ancestral haplotype in the network, were detected to be shared between Jinshajiang and Yalongjiang groups. We deduced that ancestral populations of this species might have had a continuous distribution range, which was then fragmented and isolated by the following tectonic events. Finally, the ancestral polymorphism, H2 and H5, were randomly allocated in Jinshajiang watershed and Yalongjiang watershed. Meanwhile, H5 was the dominant haplotype in Jinshajiang watershed; H7 was the domiant haplotype in Yalongjiang watershed and Wumeng Mountain. This haplotype distribution pattern indicated that each group might have served as a refuge for L. tongolensis during the Quaternary Glaciation. Postglacial demographic expansion was supported by unimodal mismatch distribution and star-like phylogenies, with expansion ages of 274 ka B. P. for this 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combination of Rodgersia, Astilboides, Darmera, Oresitrophe, Bergenia, and Mukdenia by Soltis with the name of Darmera group was supported. The key taxonomic traits of leave arrangement and pubescence were not suppoted by molecular result, especially for taxa from Hengduan Mountains and Himalayas. Multiple sampled Rodgersia aesculifolia was not monophyly, samples from Hengduan Mountains (R. henrici = R. aesculifolia var. henrici) were nested with R. pinnata and R. sambucifolia, while samples from southeast Tibet (R. henrici = R. aesculifolia var. henrici) form a clade sister to the former taxa. Samples of R. aesculifolia from Qingling and Daba mountains (R. aesculifolia var. aesculifolia = Triditional R. asculifolia) are distinct with all the above. R. aesculifolia var. henrici is distinct from A. aesculifolia var. aesculifolia and is suggested be raised to spcies level again as Rosgersia henrici Franchet. Populations of R. henrici from western Yunnan are grouping with R. pinnata, natural hybridization are supposed to occur. Rodgersia podophylla from Korea and Japan is sister to Chinese Rodgersia. The furthermore study of infraspecific taxonomy of R. aesculifolia is suggested.The relict Rodgersia nepalensis from eastern Nepal branched first in the combined ITS and plastid tree, which is different from evidences of the traditional morphology and cytology. This might due to its narrow distribution disjuct from other species of Rodgersia, low level of gene flow and subsequent conserved genetic system. It may evolved by polyploidy, the spcecialized morphological character of R. nepalensis may be a strategy for ecological tolerance and self-protection. Our molecular phylogeny of Rodgersia is accordant with the former morphological and cytological evidences. Hybridization and polyploidy may play an important role in evolution and speciation in Rodgersia. Rodgersia may origin from northestern Asia and migrated into Hengduan mountains and Himalayas through Qingling and Daba mountains. Based on present molecular results, as well as original description papers and Type specimen, six species and two variaties were recognized in Rodgersia. Rodgersia henrici was recognized in our study, and was supported to be raised to species level again","jscount":"1","jsurl":"/simple-search?field1=all&field=dc.date.issued.year&advanced=false&query1=%25E5%258C%25BA%25E7%25B3%25BB%25E7%2589%25B9%25E5%25BE%2581&&fq=dc.project.title_filter%3Athe%5C+combination%5C+of%5C+Rodgersia%2C%5C+Astilboides%2C%5C+Darmera%2C%5C+Oresitrophe%2C%5C+Bergenia%2C%5C+and%5C+Mukdenia%5C+by%5C+Soltis%5C+with%5C+the%5C+name%5C+of%5C+Darmera%5C+group%5C+was%5C+supported.%5C+The%5C+key%5C+taxonomic%5C+traits%5C+of%5C+leave%5C+arrangement%5C+and%5C+pubescence%5C+were%5C+not%5C+suppoted%5C+by%5C+molecular%5C+result%2C%5C+especially%5C+for%5C+taxa%5C+from%5C+Hengduan%5C+Mountains%5C+and%5C+Himalayas.%5C+Multiple%5C+sampled%5C+Rodgersia%5C+aesculifolia%5C+was%5C+not%5C+monophyly%2C%5C+samples%5C+from%5C+Hengduan%5C+Mountains%5C+%5C%28R.%5C+henrici%5C+%3D%5C+R.%5C+aesculifolia%5C+var.%5C+henrici%5C%29%5C+were%5C+nested%5C+with%5C+R.%5C+pinnata%5C+and%5C+R.%5C+sambucifolia%2C%5C+while%5C+samples%5C+from%5C+southeast%5C+Tibet%5C+%5C%28R.%5C+henrici%5C+%3D%5C+R.%5C+aesculifolia%5C+var.%5C+henrici%5C%29%5C+form%5C+a%5C+clade%5C+sister%5C+to%5C+the%5C+former%5C+taxa.%5C+Samples%5C+of%5C+R.%5C+aesculifolia%5C+from%5C+Qingling%5C+and%5C+Daba%5C+mountains%5C+%5C%28R.%5C+aesculifolia%5C+var.%5C+aesculifolia%5C+%3D%5C+Triditional%5C+R.%5C+asculifolia%5C%29%5C+are%5C+distinct%5C+with%5C+all%5C+the%5C+above.%5C+R.%5C+aesculifolia%5C+var.%5C+henrici%5C+is%5C+distinct%5C+from%5C+A.%5C+aesculifolia%5C+var.%5C+aesculifolia%5C+and%5C+is%5C+suggested%5C+be%5C+raised%5C+to%5C+spcies%5C+level%5C+again%5C+as%5C+Rosgersia%5C+henrici%5C+Franchet.%5C+Populations%5C+of%5C+R.%5C+henrici%5C+from%5C+western%5C+Yunnan%5C+are%5C+grouping%5C+with%5C+R.%5C+pinnata%2C%5C+natural%5C+hybridization%5C+are%5C+supposed%5C+to%5C+occur.%5C+Rodgersia%5C+podophylla%5C+from%5C+Korea%5C+and%5C+Japan%5C+is%5C+sister%5C+to%5C+Chinese%5C+Rodgersia.%5C+The%5C+furthermore%5C+study%5C+of%5C+infraspecific%5C+taxonomy%5C+of%5C+R.%5C+aesculifolia%5C+is%5C+suggested.The%5C+relict%5C+Rodgersia%5C+nepalensis%5C+from%5C+eastern%5C+Nepal%5C+branched%5C+first%5C+in%5C+the%5C+combined%5C+ITS%5C+and%5C+plastid%5C+tree%2C%5C+which%5C+is%5C+different%5C+from%5C+evidences%5C+of%5C+the%5C+traditional%5C+morphology%5C+and%5C+cytology.%5C+This%5C+might%5C+due%5C+to%5C+its%5C+narrow%5C+distribution%5C+disjuct%5C+from%5C+other%5C+species%5C+of%5C+Rodgersia%2C%5C+low%5C+level%5C+of%5C+gene%5C+flow%5C+and%5C+subsequent%5C+conserved%5C+genetic%5C+system.%5C+It%5C+may%5C+evolved%5C+by%5C+polyploidy%2C%5C+the%5C+spcecialized%5C+morphological%5C+character%5C+of%5C+R.%5C+nepalensis%5C+may%5C+be%5C+a%5C+strategy%5C+for%5C+ecological%5C+tolerance%5C+and%5C+self%5C-protection.%5C+Our%5C+molecular%5C+phylogeny%5C+of%5C+Rodgersia%5C+is%5C+accordant%5C+with%5C+the%5C+former%5C+morphological%5C+and%5C+cytological%5C+evidences.%5C+Hybridization%5C+and%5C+polyploidy%5C+may%5C+play%5C+an%5C+important%5C+role%5C+in%5C+evolution%5C+and%5C+speciation%5C+in%5C+Rodgersia.%5C+Rodgersia%5C+may%5C+origin%5C+from%5C+northestern%5C+Asia%5C+and%5C+migrated%5C+into%5C+Hengduan%5C+mountains%5C+and%5C+Himalayas%5C+through%5C+Qingling%5C+and%5C+Daba%5C+mountains.%5C+Based%5C+on%5C+present%5C+molecular%5C+results%2C%5C+as%5C+well%5C+as%5C+original%5C+description%5C+papers%5C+and%5C+Type%5C+specimen%2C%5C+six%5C+species%5C+and%5C+two%5C+variaties%5C+were%5C+recognized%5C+in%5C+Rodgersia.%5C+Rodgersia%5C+henrici%5C+was%5C+recognized%5C+in%5C+our%5C+study%2C%5C+and%5C+was%5C+supported%5C+to%5C+be%5C+raised%5C+to%5C+species%5C+level%5C+again"},{"jsname":"lastIndexed","jscount":"2024-04-20"}],"资助项目","dc.project.title_filter")'>
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