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中国科学院昆明植物研究所知识管理系统
Knowledge Management System of Kunming Institute of Botany,CAS
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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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Taxus wallichiana complex represents an old relict conifer lineage that survived through the Tertiary. It is currently distributed in the mountain forests in South and Southwest China south of the Qinling Mountains. In the present study, we explored phylogeography of the complex by using two chloroplast DNA regions, one nuclear ribosomal DNA spacer region and eight microsatellite (SSR) loci. The main conclusions can be summarized as follows:1. Phylogeographic pattern based on chloroplast haplotypes，There were 11 cpDNA haplotypes identified in the T. wallichiana complex The complex showed a high level of genetic diversity and obvious genetic differentiation. The 44 sampled populations showed obvious genetic structure, which could be divided into five groups, namely the Huanan group, the Daba group, the Emei group, the Yunnan group and the Qinling group. There was extremely high genetic differentiation among groups, but not significant within group. The divergence times of the five lineages, estimated using average mutation rates of trnL-trnF, fell in the Pliocene. 2. Phylogeographic patterns based on ITS sequences，These included 38 unique ‘haplotypes’ based on ITS data. Their analysis showed that the T. wallichiana complex possessed a high genetic diversity. These populations could be divided into four groups, namely the Huanan group, the Daba/Emei group, the Yunnan group and the Qinling group. Based on all results, it appears that the major lineages constituting the T. wallichiana complex have arisen before Quaternary glaciation cycles, and may have survived isolated in different refugia. During interglacial periods some lineages appear to have come in contact and hybridizedbut other lineages merged forming populations with mixed haplotypes without signs of hybridization. The present-day phylogeographical distribution pattern of the T. wallichiana complex might thus be the result of repeated expansion / contractions of populations during interglacial / glacial cycles.3. Population genetic analysis using microsatellite (SSR) markers，Eight SSR loci were used for population genetic analysis on the T. wallichiana complex. A lower level of genetic diversity at the population level and high genetic differentiation among population was detected. The results of structure analysis were similar to those on the ITS data, dividing the populations into four groups (lineages). According to the results here, it was deduced that each of the 4 lineages of the T. wallichiana complex may possessed respective glacial refugia, and some lineages (such as the Qinling and Huanan lineage) might have survived in multiple refugia in the Quaternay glaciations. The present distribution pattern of this complex was likely influenced by the uplift of the QTP and Quaternary glaciation.","jscount":"1","jsurl":"/simple-search?field1=all&rpp=10&accurate=false&advanced=false&sort_by=2&isNonaffiliated=false&search_type=-1&query1=%25E5%2588%2586%25E5%25AD%2590%25E7%25B3%25BB%25E7%25BB%259F%25E5%25AD%25A6&order=desc&&fq=dc.project.title_filter%3AThe%5C+Taxus%5C+wallichiana%5C+complex%5C+represents%5C+an%5C+old%5C+relict%5C+conifer%5C+lineage%5C+that%5C+survived%5C+through%5C+the%5C+Tertiary.%5C+It%5C+is%5C+currently%5C+distributed%5C+in%5C+the%5C+mountain%5C+forests%5C+in%5C+South%5C+and%5C+Southwest%5C+China%5C+south%5C+of%5C+the%5C+Qinling%5C+Mountains.%C2%A0In%5C+the%5C+present%5C+study%2C%5C+we%5C+explored%5C+phylogeography%5C+of%5C+the%5C+complex%5C+by%5C+using%5C+two%5C+chloroplast%5C+DNA%5C+regions%2C%5C+one%5C+nuclear%5C+ribosomal%5C+DNA%5C+spacer%5C+region%5C+and%5C+eight%5C+microsatellite%5C+%5C%28SSR%5C%29%5C+loci.%5C+The%5C+main%5C+conclusions%5C+can%5C+be%5C+summarized%5C+as%5C+follows%5C%3A1.%5C+Phylogeographic%5C+pattern%5C+based%5C+on%5C+chloroplast%5C+haplotypes%EF%BC%8CThere%5C+were%5C+11%5C+cpDNA%5C+haplotypes%5C+identified%5C+in%5C+the%5C+T.%5C+wallichiana%5C+complex%5C+The%5C+complex%5C+showed%5C+a%5C+high%5C+level%5C+of%5C+genetic%5C+diversity%5C+and%5C+obvious%5C+genetic%5C+differentiation.%5C+The%5C+44%5C+sampled%5C+populations%5C+showed%5C+obvious%5C+genetic%5C+structure%2C%5C+which%5C+could%5C+be%5C+divided%5C+into%5C+five%5C+groups%2C%5C+namely%5C+the%5C+Huanan%5C+group%2C%5C+the%5C+Daba%5C+group%2C%5C+the%5C+Emei%5C+group%2C%5C+the%5C+Yunnan%5C+group%5C+and%5C+the%5C+Qinling%5C+group.%5C+There%5C+was%5C+extremely%5C+high%5C+genetic%5C+differentiation%5C+among%5C+groups%2C%5C+but%5C+not%5C+significant%5C+within%5C+group.%5C+The%5C+divergence%5C+times%5C+of%5C+the%5C+five%5C+lineages%2C%5C+estimated%5C+using%5C+average%5C+mutation%5C+rates%5C+of%5C+trnL%5C-trnF%2C%5C+fell%5C+in%5C+the%5C+Pliocene.%C2%A02.%5C+Phylogeographic%5C+patterns%5C+based%5C+on%5C+ITS%5C+sequences%EF%BC%8CThese%5C+included%5C+38%5C+unique%5C+%E2%80%98haplotypes%E2%80%99%5C+based%5C+on%5C+ITS%5C+data.%5C+Their%5C+analysis%5C+showed%5C+that%5C+the%5C+T.%5C+wallichiana%5C+complex%5C+possessed%5C+a%5C+high%5C+genetic%5C+diversity.%C2%A0These%5C+populations%5C+could%5C+be%5C+divided%5C+into%5C+four%5C+groups%2C%5C+namely%5C+the%5C+Huanan%5C+group%2C%5C+the%5C+Daba%5C%2FEmei%5C+group%2C%5C+the%5C+Yunnan%5C+group%5C+and%5C+the%5C+Qinling%5C+group.%5C+Based%5C+on%5C+all%5C+results%2C%5C+it%5C+appears%5C+that%5C+the%5C+major%5C+lineages%5C+constituting%5C+the%5C+T.%5C+wallichiana%5C+complex%5C+have%5C+arisen%5C+before%5C+Quaternary%5C+glaciation%5C+cycles%2C%5C+and%5C+may%5C+have%5C+survived%5C+isolated%5C+in%5C+different%5C+refugia.%5C+During%5C+interglacial%5C+periods%5C+some%5C+lineages%5C+appear%5C+to%5C+have%5C+come%5C+in%5C+contact%5C+and%5C+hybridizedbut%5C+other%5C+lineages%5C+merged%5C+forming%5C+populations%5C+with%5C+mixed%5C+haplotypes%5C+without%5C+signs%5C+of%5C+hybridization.%5C+The%5C+present%5C-day%5C+phylogeographical%5C+distribution%5C+pattern%5C+of%5C+the%5C+T.%5C+wallichiana%5C+complex%5C+might%5C+thus%5C+be%5C+the%5C+result%5C+of%5C+repeated%5C+expansion%5C+%5C%2F%5C+contractions%5C+of%5C+populations%5C+during%5C+interglacial%5C+%5C%2F%5C+glacial%5C+cycles.3.%5C+Population%5C+genetic%5C+analysis%5C+using%5C+microsatellite%5C+%5C%28SSR%5C%29%5C+markers%EF%BC%8CEight%5C+SSR%5C+loci%5C+were%5C+used%5C+for%5C+population%5C+genetic%5C+analysis%5C+on%5C+the%5C+T.%5C+wallichiana%5C+complex.%5C+A%5C+lower%5C+level%5C+of%5C+genetic%5C+diversity%5C+at%5C+the%5C+population%5C+level%5C+and%5C+high%5C+genetic%5C+differentiation%5C+among%5C+population%5C+was%5C+detected.%5C+The%5C+results%5C+of%5C+structure%5C+analysis%5C+were%5C+similar%5C+to%5C+those%5C+on%5C+the%5C+ITS%5C+data%2C%5C+dividing%5C+the%5C+populations%5C+into%5C+four%5C+groups%5C+%5C%28lineages%5C%29.%C2%A0According%5C+to%5C+the%5C+results%5C+here%2C%5C+it%5C+was%5C+deduced%5C+that%5C+each%5C+of%5C+the%5C+4%5C+lineages%5C+of%5C+the%5C+T.%5C+wallichiana%5C+complex%5C+may%5C+possessed%5C+respective%5C+glacial%5C+refugia%2C%5C+and%5C+some%5C+lineages%5C+%5C%28such%5C+as%5C+the%5C+Qinling%5C+and%5C+Huanan%5C+lineage%5C%29%5C+might%5C+have%5C+survived%5C+in%5C+multiple%5C+refugia%5C+in%5C+the%5C+Quaternay%5C+glaciations.%5C+The%5C+present%5C+distribution%5C+pattern%5C+of%5C+this%5C+complex%5C+was%5C+likely%5C+influenced%5C+by%5C+the%5C+uplift%5C+of%5C+the%5C+QTP%5C+and%5C+Quaternary%5C+glaciation."},{"jsname":"The genus Clematis, with about 355 species, is one of the largest genera of Ranunculaceae. The genus is distributed through out the world except Antarctica, primarily in temperate and subtropical zone. Numerous infra-generic classification systems have been proposed, whereas the infra-generic ranks were confusing. In the present study, we used four molecular regions, ITS, psbA-trnH, atpB-rbcL and rpoB-trnC to reconstruct the phylogeny of Clematis. On the basis of comparison with traditional classification system, criteria of the infra-generic ranks are discussed. In addition, investigations of reproductive biology and seed germination were also conducted. The main important results and conclusions are as follows: 1. Species diversity and geographical distribution of the Genus Clematis in Yunnan province，According to the latest system of Wang and Li in 2005, there are 59 species and 24 varieties in 6 sections of 3 subgenera recognized within the genus of Clematis in Yunnan, which is the richest province in terms of species numbers in China. The Hengduan Mountains is regarded as an origination, differentiation and endemic center of the genus. West, Northwest and Northeast of Yunnan have some relationship with its differentiation. There are 56 species (including varieties) endemic to China, accounting for 67.2% of Yunnan’s total number of species. There are 16 species (including varieties) endemic to Yunnan, accounting for 35.0% of China’s endemic number of species distributed in Yunnan. Among the adjacent provinces, Sichuan has the largest common number of Clematis to Yunnan, while Tibet has the smallest. The floristic links with Myanmar is also relatively weak.2. Molecular phylogeny of Clematis,Phylogenetic relationships within and out of Clematis were analysed using nucleotide sequences of chloroplast DNA psbA-trnQ, atpB-rbcL and rpoB-trnC, and the nuclear ITS regions. The phylogenetic trees suggested that the genus Clematis was paraphyletic. The genera Archiclematis and Naravelia were found to be nested within the genus Clematis, and should be included in it. The molecular results did not agree with Wang and Li’s taxonomic system and other classifications of Clematis at the phylogeneric level. And the sections we studied were found to be paraphyletic or polyphyletic. The complicated relationship between sections and species indicated the recent radiation of the genus and the possibility of hybrid origin. Our results suggested that flower characters which have been used for previous infrageneric classification do not correlate with the phylogenic tree. Phyllotaxy of seedlings as the primarily diagnostic characters may reflect the phylogeny within Clematis, the following characters should be considered at the same time: presence/absence of petals, carpel number, and flowering at the new-born\\former-born branches. 3. Nomenclature notes of Clematis and other plants,Two gatherings of Clematis chrysocoma Franchet and Anemoclama glaucifolia (Franchet) W. T. Wang were cited in the protologues, whereas none of them was indicated as type or holotype. After examining the cited specimens, we designate one specimen of them as lectotype in according with ICBN. We list the incorrect author(s) citation of infra-generic names by Wang and Li in their new Clematis classification systems. Additionally, four names, Atalantia acuminata C. C. Huang, Asarum longerhizomatosum C. F. Liang & C. S. Yang, Atalantia fongkaica C. C. Huang and Fortunella wawangica C. C. Huang, are validated.4. Reproductive biology of three Clematis species,An integrative study was undertaken, focusing on pollination and reproductive biology of three species representing all three floral types of Clematis. Floral traits were measured, and pollinator assemblages were observed in the field. Bagging, hand-pollination and removal treatments were used to examine breeding system. The values of inbreeding depression and pollen limitation were calculated based on experimental data obtained from breeding system. Their floral traits were distinctly different. Floral traits were highly associated with pollination syndrome and breeding system. Among them, Clematis akebioides and C. rehderiana were facultative autogamy (the former was delayed selfing, and the later competing selfing), and C. chrysocoma was nearly obligate outcrossing. This conclusion was reflected by their stamen-pistil ratios. The levels of inbreeding depression negatively associated with autonomous self-pollination. Selfing evolution of C. akebioides and C. rehderiana, and reproduction of the three Clematis species no pollen limitation were discussed. Present study integrating with previous results will help us to comprehensively recognize and understand pollination system and reproductive characteristics of Clematis.5. Correlation among floral traits of Clematis chrysocoma, Floral traits of C. chrysocoma including sepal length and width and anther length were measured, stamen and pistil number were counted, single and total sepal size, and total anther size were calculated in three continued years from 2007 to 2009. These traits of three years were analyzed as united and independent data, respectively, which was used to compare the stability of floral traits among three years, and to test sexual allocation theory. Our results show that floral traits except sepal length are stable in three continued years, correlation among floral traits of three years as whole and independence, respectively, some of which are consistent, and some of which are inconsistent or negative. The consistent traits demonstrate that they highly co-evolve, whereas the inconsistent or negative traits may be results from the stochastically errors or that they may have some correlation but not close. Association of stamen number with anther length is not negative, but with pistil number is significantly positive. Correlation among pistil number, total anther size and total sepal size, all of that are significantly positive. Therefore, sexual allocation strategies of C. chrysocoma should be determined by genetics and resource pool in contrary to the model of “compensation” as traditionally view.6. Seed germination of six Clematis species,Seed germination of six species of Clematis were studied by setting different conditions including pretreatment, GA3 treatments, light and temperature regimes, and substrates. The results of the test were as follows: flushing treatment had a significant promoting on seed germination percentage and mean germination time (MGT)","jscount":"1","jsurl":"/simple-search?field1=all&rpp=10&accurate=false&advanced=false&sort_by=2&isNonaffiliated=false&search_type=-1&query1=%25E5%2588%2586%25E5%25AD%2590%25E7%25B3%25BB%25E7%25BB%259F%25E5%25AD%25A6&order=desc&&fq=dc.project.title_filter%3AThe%5C+genus%5C+Clematis%2C%5C+with%5C+about%5C+355%5C+species%2C%5C+is%5C+one%5C+of%5C+the%5C+largest%5C+genera%5C+of%5C+Ranunculaceae.%5C+The%5C+genus%5C+is%5C+distributed%5C+through%5C+out%5C+the%5C+world%5C+except%5C+Antarctica%2C%5C+primarily%5C+in%5C+temperate%5C+and%5C+subtropical%5C+zone.%5C+Numerous%5C+infra%5C-generic%5C+classification%5C+systems%5C+have%5C+been%5C+proposed%2C%5C+whereas%5C+the%5C+infra%5C-generic%5C+ranks%5C+were%5C+confusing.%5C+In%5C+the%5C+present%5C+study%2C%5C+we%5C+used%5C+four%5C+molecular%5C+regions%2C%5C+ITS%2C%5C+psbA%5C-trnH%2C%5C+atpB%5C-rbcL%5C+and%5C+rpoB%5C-trnC%5C+to%5C+reconstruct%5C+the%5C+phylogeny%5C+of%5C+Clematis.%5C+On%5C+the%5C+basis%5C+of%5C+comparison%5C+with%5C+traditional%5C+classification%5C+system%2C%5C+criteria%5C+of%5C+the%5C+infra%5C-generic%5C+ranks%5C+are%5C+discussed.%5C+In%5C+addition%2C%5C+investigations%5C+of%5C+reproductive%5C+biology%5C+and%5C+seed%5C+germination%5C+were%5C+also%5C+conducted.%5C+The%5C+main%5C+important%5C+results%5C+and%5C+conclusions%5C+are%5C+as%5C+follows%5C%3A%5C+1.%5C+Species%5C+diversity%5C+and%5C+geographical%5C+distribution%5C+of%5C+the%5C+Genus%5C+Clematis%5C+in%5C+Yunnan%5C+province%EF%BC%8CAccording%5C+to%5C+the%5C+latest%5C+system%5C+of%5C+Wang%5C+and%5C+Li%5C+in%5C+2005%2C%5C+there%5C+are%5C+59%5C+species%5C+and%5C+24%5C+varieties%5C+in%5C+6%5C+sections%5C+of%5C+3%5C+subgenera%5C+recognized%5C+within%5C+the%5C+genus%5C+of%5C+Clematis%5C+in%5C+Yunnan%2C%5C+which%5C+is%5C+the%5C+richest%5C+province%5C+in%5C+terms%5C+of%5C+species%5C+numbers%5C+in%5C+China.%5C+The%5C+Hengduan%5C+Mountains%5C+is%5C+regarded%5C+as%5C+an%5C+origination%2C%5C+differentiation%5C+and%5C+endemic%5C+center%5C+of%5C+the%5C+genus.%5C+West%2C%5C+Northwest%5C+and%5C+Northeast%5C+of%5C+Yunnan%5C+have%5C+some%5C+relationship%5C+with%5C+its%5C+differentiation.%5C+There%5C+are%5C+56%5C+species%5C+%5C%28including%5C+varieties%5C%29%5C+endemic%5C+to%5C+China%2C%5C+accounting%5C+for%5C+67.2%25%5C+of%5C+Yunnan%E2%80%99s%5C+total%5C+number%5C+of%5C+species.%5C+There%5C+are%5C+16%5C+species%5C+%5C%28including%5C+varieties%5C%29%5C+endemic%5C+to%5C+Yunnan%2C%5C+accounting%5C+for%5C+35.0%25%5C+of%5C+China%E2%80%99s%5C+endemic%5C+number%5C+of%5C+species%5C+distributed%5C+in%5C+Yunnan.%5C+Among%5C+the%5C+adjacent%5C+provinces%2C%5C+Sichuan%5C+has%5C+the%5C+largest%5C+common%5C+number%5C+of%5C+Clematis%5C+to%5C+Yunnan%2C%5C+while%5C+Tibet%5C+has%5C+the%5C+smallest.%5C+The%5C+floristic%5C+links%5C+with%5C+Myanmar%5C+is%5C+also%5C+relatively%5C+weak.2.%5C+Molecular%5C+phylogeny%5C+of%5C+Clematis%2CPhylogenetic%5C+relationships%5C+within%5C+and%5C+out%5C+of%5C+Clematis%5C+were%5C+analysed%5C+using%5C+nucleotide%5C+sequences%5C+of%5C+chloroplast%5C+DNA%5C+psbA%5C-trnQ%2C%5C+atpB%5C-rbcL%5C+and%5C+rpoB%5C-trnC%2C%5C+and%5C+the%5C+nuclear%5C+ITS%5C+regions.%5C+The%5C+phylogenetic%5C+trees%5C+suggested%5C+that%5C+the%5C+genus%5C+Clematis%5C+was%5C+paraphyletic.%5C+The%5C+genera%5C+Archiclematis%5C+and%5C+Naravelia%5C+were%5C+found%5C+to%5C+be%5C+nested%5C+within%5C+the%5C+genus%5C+Clematis%2C%5C+and%5C+should%5C+be%5C+included%5C+in%5C+it.%5C+The%5C+molecular%5C+results%5C+did%5C+not%5C+agree%5C+with%5C+Wang%5C+and%5C+Li%E2%80%99s%5C+taxonomic%5C+system%5C+and%5C+other%5C+classifications%5C+of%5C+Clematis%5C+at%5C+the%5C+phylogeneric%5C+level.%5C+And%5C+the%5C+sections%5C+we%5C+studied%5C+were%5C+found%5C+to%5C+be%5C+paraphyletic%5C+or%5C+polyphyletic.%5C+The%5C+complicated%5C+relationship%5C+between%5C+sections%5C+and%5C+species%5C+indicated%5C+the%5C+recent%5C+radiation%5C+of%5C+the%5C+genus%5C+and%5C+the%5C+possibility%5C+of%5C+hybrid%5C+origin.%5C+Our%5C+results%5C+suggested%5C+that%5C+flower%5C+characters%5C+which%5C+have%5C+been%5C+used%5C+for%5C+previous%5C+infrageneric%5C+classification%5C+do%5C+not%5C+correlate%5C+with%5C+the%5C+phylogenic%5C+tree.%5C+Phyllotaxy%5C+of%5C+seedlings%5C+as%5C+the%5C+primarily%5C+diagnostic%5C+characters%5C+may%5C+reflect%5C+the%5C+phylogeny%5C+within%5C+Clematis%2C%5C+the%5C+following%5C+characters%5C+should%5C+be%5C+considered%5C+at%5C+the%5C+same%5C+time%5C%3A%5C+presence%5C%2Fabsence%5C+of%5C+petals%2C%5C+carpel%5C+number%2C%5C+and%5C+flowering%5C+at%5C+the%5C+new%5C-born%5C%5Cformer%5C-born%5C+branches.%5C+3.%5C+Nomenclature%5C+notes%5C+of%5C+Clematis%5C+and%5C+other%5C+plants%2CTwo%5C+gatherings%5C+of%5C+Clematis%5C+chrysocoma%5C+Franchet%5C+and%5C+Anemoclama%5C+glaucifolia%5C+%5C%28Franchet%5C%29%5C+W.%5C+T.%5C+Wang%5C+were%5C+cited%5C+in%5C+the%5C+protologues%2C%5C+whereas%5C+none%5C+of%5C+them%5C+was%5C+indicated%5C+as%5C+type%5C+or%5C+holotype.%5C+After%5C+examining%5C+the%5C+cited%5C+specimens%2C%5C+we%5C+designate%5C+one%5C+specimen%5C+of%5C+them%5C+as%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temperate woody bamboos are a morphologically diverse group with a complicated taxonomy. The Arundinaria group has an East Asia-North America disjunct distribution, which is one of those with complex taxonomy in the temperate woody bamboos. In this study, the phylogeny of the temperate woody bamboos was reconstructed based on eight non-coding regions of the chloroplast genome and nuclear gene GBSSI using large sample set (124 species in 24 genera) with an emphasis on the Arundinaria group. The monophyly of the temperate woody bamboos was resolved in all phylogenies. Ten major lineages were obtained in the chloroplast phylogeny with unresolved relationships among them; the recovered phylogeny is strongly incongruent with the classifications based on morphology at both subtribal and generic ranks; some subclades that are related to the geographic distribution were obtained in those lineages. Five lineages in the GBSSI gene phylogeny were recovered as the same in the chloroplast phylogeny, and the other lineages were incongruent with chloroplast phylogeny in some ways. The reticulate evolution caused by hybridization, introgression and lineage sorting may be an explanation for the molecular phylogenetic incongruence. Based on the facts of diverse morphology, broad distribution and molecular phylogeny, we inferred that the major clades and species within most of the clades of the temperate woody bamboos were originated during several rapid adaptive radiations. Ten putative hybrids were discussed based on molecular phylogenies, morphology and distribution. The micromorphology of the leaf epidermis under SEM (scanning electron microscope) was observed and divided into nine types; the micromorphology can provide some evidence for the bamboo taxonomy and inference of putative hybrids. Additionally, taxonomic revisions were presented for some species based on field observation and herbarium work.","jscount":"1","jsurl":"/simple-search?field1=all&rpp=10&accurate=false&advanced=false&sort_by=2&isNonaffiliated=false&search_type=-1&query1=%25E5%2588%2586%25E5%25AD%2590%25E7%25B3%25BB%25E7%25BB%259F%25E5%25AD%25A6&order=desc&&fq=dc.project.title_filter%3AThe%5C+temperate%5C+woody%5C+bamboos%5C+are%5C+a%5C+morphologically%5C+diverse%5C+group%5C+with%5C+a%5C+complicated%5C+taxonomy.%5C+The%5C+Arundinaria%5C+group%5C+has%5C+an%5C+East%5C+Asia%5C-North%5C+America%5C+disjunct%5C+distribution%2C%5C+which%5C+is%5C+one%5C+of%5C+those%5C+with%5C+complex%5C+taxonomy%5C+in%5C+the%5C+temperate%5C+woody%5C+bamboos.%5C+In%5C+this%5C+study%2C%5C+the%5C+phylogeny%5C+of%5C+the%5C+temperate%5C+woody%5C+bamboos%5C+was%5C+reconstructed%5C+based%5C+on%5C+eight%5C+non%5C-coding%5C+regions%5C+of%5C+the%5C+chloroplast%5C+genome%5C+and%5C+nuclear%5C+gene%5C+GBSSI%5C+using%5C+large%5C+sample%5C+set%5C+%5C%28124%5C+species%5C+in%5C+24%5C+genera%5C%29%5C+with%5C+an%5C+emphasis%5C+on%5C+the%5C+Arundinaria%5C+group.%5C+The%5C+monophyly%5C+of%5C+the%5C+temperate%5C+woody%5C+bamboos%5C+was%5C+resolved%5C+in%5C+all%5C+phylogenies.%5C+Ten%5C+major%5C+lineages%5C+were%5C+obtained%5C+in%5C+the%5C+chloroplast%5C+phylogeny%5C+with%5C+unresolved%5C+relationships%5C+among%5C+them%5C%3B%5C+the%5C+recovered%5C+phylogeny%5C+is%5C+strongly%5C+incongruent%5C+with%5C+the%5C+classifications%5C+based%5C+on%5C+morphology%5C+at%5C+both%5C+subtribal%5C+and%5C+generic%5C+ranks%5C%3B%5C+some%5C+subclades%5C+that%5C+are%5C+related%5C+to%5C+the%5C+geographic%5C+distribution%5C+were%5C+obtained%5C+in%5C+those%5C+lineages.%5C+Five%5C+lineages%5C+in%5C+the%5C+GBSSI%5C+gene%5C+phylogeny%5C+were%5C+recovered%5C+as%5C+the%5C+same%5C+in%5C+the%5C+chloroplast%5C+phylogeny%2C%5C+and%5C+the%5C+other%5C+lineages%5C+were%5C+incongruent%5C+with%5C+chloroplast%5C+phylogeny%5C+in%5C+some%5C+ways.%5C+The%5C+reticulate%5C+evolution%5C+caused%5C+by%5C+hybridization%2C%5C+introgression%5C+and%5C+lineage%5C+sorting%5C+may%5C+be%5C+an%5C+explanation%5C+for%5C+the%5C+molecular%5C+phylogenetic%5C+incongruence.%5C+Based%5C+on%5C+the%5C+facts%5C+of%5C+diverse%5C+morphology%2C%5C+broad%5C+distribution%5C+and%5C+molecular%5C+phylogeny%2C%5C+we%5C+inferred%5C+that%5C+the%5C+major%5C+clades%5C+and%5C+species%5C+within%5C+most%5C+of%5C+the%5C+clades%5C+of%5C+the%5C+temperate%5C+woody%5C+bamboos%5C+were%5C+originated%5C+during%5C+several%5C+rapid%5C+adaptive%5C+radiations.%5C+Ten%5C+putative%5C+hybrids%5C+were%5C+discussed%5C+based%5C+on%5C+molecular%5C+phylogenies%2C%5C+morphology%5C+and%5C+distribution.%5C+The%5C+micromorphology%5C+of%5C+the%5C+leaf%5C+epidermis%5C+under%5C+SEM%5C+%5C%28scanning%5C+electron%5C+microscope%5C%29%5C+was%5C+observed%5C+and%5C+divided%5C+into%5C+nine%5C+types%5C%3B%5C+the%5C+micromorphology%5C+can%5C+provide%5C+some%5C+evidence%5C+for%5C+the%5C+bamboo%5C+taxonomy%5C+and%5C+inference%5C+of%5C+putative%5C+hybrids.%5C+Additionally%2C%5C+taxonomic%5C+revisions%5C+were%5C+presented%5C+for%5C+some%5C+species%5C+based%5C+on%5C+field%5C+observation%5C+and%5C+herbarium%5C+work."},{"jsname":"Through investigating sympatric distribution of Rhododendron irroratum, examing the variation of floral characters and sequencing the ITS and other chloroplast segements, we find that (1) R. irroratum might be of hybrid origin, with its maternal parent R. delavayi or R. decorum. (2) The ancestral haplotype of R. irroratum might be identical to that of R. decorum, and it is under ongoing introgression from R. delavayi. 1. The natural distribution, Seven distribution sites of R. irroratum in Guizhou and Yunnan province were investigated. The result shows that R. irroratum is sympatric with R. delavayi, R. decorum and R. agastum. R. delavayi is widespread across the above-mentioned seven sites, whereas R. agastum is scarce in DaPingDi, HuaDianBa and HeQing sites. R. irroratum and R. agastum distribute at the higher elevation compared to that of R. decorum, while R. delavayi is of widespread distribution across both regions of R. decorum and R. irroratum.2. Floral variation of R. irroratum among populations, The floral characters remain vary within and among populations except for the stamen number and the petal number. Seven floral characters correlates with each other among populations, of 28 different combinations, 26 reveal significant correlation, and 23 extremely significant correlation. The PCA analysis shows that the first two components account for 52.18% of the total variation. The dendrogram tree is divided into four main parts, roughly representing the respective populations, which is constructed using 22 R. irroratum individuals. 3. Putative Development and the transferability test of SSR makers, Fifteen microsatellite loci were developed and characterized in R. delavayi. The average allele number of these microsatellites was 4 per locus, ranging from 3 to 6. The ranges of expected (HE) and observed (HO) heterozygosities were 0.0365-0.7091 and 0.0263-0.9512, respectively. Seven loci (R-111, R-112, R-147, R-299, R-320, R-335, and R-544) deviated significantly from the HWE (P﹤0.01). No significant linkage disequilibrium was detected between locus pairs except for three locus pairs: R-299 and R-544, R-166 and R-320, R-111 and R-320. Cross-species amplification in R. agastum, R. decorum, and R. irroratum showed that a subset of these markers holds promise for congeneric species study.4. ITS, matK, trnH-psbA and rbcL sequences. R. delavayi has six sites different from that of R. decorum in its ITS region, whereas R. agastum reveals double peaks at the corresponding sites and R. irroratum is identical to that of R. delavayi. The chloroplast segements show that some R. irroratum individuals share the same haplotype with R. delavayi and others share them with R. decorum.","jscount":"1","jsurl":"/simple-search?field1=all&rpp=10&accurate=false&advanced=false&sort_by=2&isNonaffiliated=false&search_type=-1&query1=%25E5%2588%2586%25E5%25AD%2590%25E7%25B3%25BB%25E7%25BB%259F%25E5%25AD%25A6&order=desc&&fq=dc.project.title_filter%3AThrough%5C+investigating%5C+sympatric%5C+distribution%5C+of%5C+Rhododendron%5C+irroratum%2C%5C+examing%5C+the%5C+variation%5C+of%5C+floral%5C+characters%5C+and%5C+sequencing%5C+the%5C+ITS%5C+and%5C+other%5C+chloroplast%5C+segements%2C%5C+we%5C+find%5C+that%5C+%5C%281%5C%29%5C+R.%5C+irroratum%5C+might%5C+be%5C+of%5C+hybrid%5C+origin%2C%5C+with%5C+its%5C+maternal%5C+parent%5C+R.%5C+delavayi%5C+or%5C+R.%5C+decorum.%5C+%5C%282%5C%29%5C+The%5C+ancestral%5C+haplotype%5C+of%5C+R.%5C+irroratum%5C+might%5C+be%5C+identical%5C+to%5C+that%5C+of%5C+R.%5C+decorum%2C%5C+and%5C+it%5C+is%5C+under%5C+ongoing%5C+introgression%5C+from%5C+R.%5C+delavayi.%5C+1.%5C+The%5C+natural%5C+distribution%2C%5C+Seven%5C+distribution%5C+sites%5C+of%5C+R.%5C+irroratum%5C+in%5C+Guizhou%5C+and%5C+Yunnan%5C+province%5C+were%5C+investigated.%5C+The%5C+result%5C+shows%5C+that%5C+R.%5C+irroratum%5C+is%5C+sympatric%5C+with%5C+R.%5C+delavayi%2C%5C+R.%5C+decorum%5C+and%5C+R.%5C+agastum.%5C+R.%5C+delavayi%5C+is%5C+widespread%5C+across%5C+the%5C+above%5C-mentioned%5C+seven%5C+sites%2C%5C+whereas%5C+R.%5C+agastum%5C+is%5C+scarce%5C+in%5C+DaPingDi%2C%5C+HuaDianBa%5C+and%5C+HeQing%5C+sites.%5C+R.%5C+irroratum%5C+and%5C+R.%5C+agastum%5C+distribute%5C+at%5C+the%5C+higher%5C+elevation%5C+compared%5C+to%5C+that%5C+of%5C+R.%5C+decorum%2C%5C+while%5C+R.%5C+delavayi%5C+is%5C+of%5C+widespread%5C+distribution%5C+across%5C+both%5C+regions%5C+of%5C+R.%5C+decorum%5C+and%5C+R.%5C+irroratum.2.%5C+Floral%5C+variation%5C+of%5C+R.%5C+irroratum%5C+among%5C+populations%2C%5C+The%5C+floral%5C+characters%5C+remain%5C+vary%5C+within%5C+and%5C+among%5C+populations%5C+except%5C+for%5C+the%5C+stamen%5C+number%5C+and%5C+the%5C+petal%5C+number.%5C+Seven%5C+floral%5C+characters%5C+correlates%5C+with%5C+each%5C+other%5C+among%5C+populations%2C%5C+of%5C+28%5C+different%5C+combinations%2C%5C+26%5C+reveal%5C+significant%5C+correlation%2C%5C+and%5C+23%5C+extremely%5C+significant%5C+correlation.%5C+The%5C+PCA%5C+analysis%5C+shows%5C+that%5C+the%5C+first%5C+two%5C+components%5C+account%5C+for%5C+52.18%25%5C+of%5C+the%5C+total%5C+variation.%5C+The%5C+dendrogram%5C+tree%5C+is%5C+divided%5C+into%5C+four%5C+main%5C+parts%2C%5C+roughly%5C+representing%5C+the%5C+respective%5C+populations%2C%5C+which%5C+is%5C+constructed%5C+using%5C+22%5C+R.%5C+irroratum%5C+individuals.%5C+3.%5C+Putative%5C+Development%5C+and%5C+the%5C+transferability%5C+test%5C+of%5C+SSR%5C+makers%2C%5C+Fifteen%5C+microsatellite%5C+loci%5C+were%5C+developed%5C+and%5C+characterized%5C+in%5C+R.%5C+delavayi.%5C+The%5C+average%5C+allele%5C+number%5C+of%5C+these%5C+microsatellites%5C+was%5C+4%5C+per%5C+locus%2C%5C+ranging%5C+from%5C+3%5C+to%5C+6.%5C+The%5C+ranges%5C+of%5C+expected%5C+%5C%28HE%5C%29%5C+and%5C+observed%5C+%5C%28HO%5C%29%5C+heterozygosities%5C+were%5C+0.0365%5C-0.7091%5C+and%5C+0.0263%5C-0.9512%2C%5C+respectively.%5C+Seven%5C+loci%5C+%5C%28R%5C-111%2C%5C+R%5C-112%2C%5C+R%5C-147%2C%5C+R%5C-299%2C%5C+R%5C-320%2C%5C+R%5C-335%2C%5C+and%5C+R%5C-544%5C%29%5C+deviated%5C+significantly%5C+from%5C+the%5C+HWE%5C+%5C%28P%EF%B9%A40.01%5C%29.%5C+No%5C+significant%5C+linkage%5C+disequilibrium%5C+was%5C+detected%5C+between%5C+locus%5C+pairs%5C+except%5C+for%5C+three%5C+locus%5C+pairs%5C%3A%5C+R%5C-299%5C+and%5C+R%5C-544%2C%5C+R%5C-166%5C+and%5C+R%5C-320%2C%5C+R%5C-111%5C+and%5C+R%5C-320.%5C+Cross%5C-species%5C+amplification%5C+in%5C+R.%5C+agastum%2C%5C+R.%5C+decorum%2C%5C+and%5C+R.%5C+irroratum%5C+showed%5C+that%5C+a%5C+subset%5C+of%5C+these%5C+markers%5C+holds%5C+promise%5C+for%5C+congeneric%5C+species%5C+study.4.%5C+ITS%2C%5C+matK%2C%5C+trnH%5C-psbA%5C+and%5C+rbcL%5C+sequences.%5C+R.%5C+delavayi%5C+has%5C+six%5C+sites%5C+different%5C+from%5C+that%5C+of%5C+R.%5C+decorum%5C+in%5C+its%5C+ITS%5C+region%2C%5C+whereas%5C+R.%5C+agastum%5C+reveals%5C+double%5C+peaks%5C+at%5C+the%5C+corresponding%5C+sites%5C+and%5C+R.%5C+irroratum%5C+is%5C+identical%5C+to%5C+that%5C+of%5C+R.%5C+delavayi.%5C+The%5C+chloroplast%5C+segements%5C+show%5C+that%5C+some%5C+R.%5C+irroratum%5C+individuals%5C+share%5C+the%5C+same%5C+haplotype%5C+with%5C+R.%5C+delavayi%5C+and%5C+others%5C+share%5C+them%5C+with%5C+R.%5C+decorum."},{"jsname":"and germination of the seeds soaked in low concentrations GA3 was a little higher than those of others. The seeds in perlite had the highest germination percentage than those in other substrates.","jscount":"1","jsurl":"/simple-search?field1=all&rpp=10&accurate=false&advanced=false&sort_by=2&isNonaffiliated=false&search_type=-1&query1=%25E5%2588%2586%25E5%25AD%2590%25E7%25B3%25BB%25E7%25BB%259F%25E5%25AD%25A6&order=desc&&fq=dc.project.title_filter%3Aand%5C+germination%5C+of%5C+the%5C+seeds%5C+soaked%5C+in%5C+low%5C+concentrations%5C+GA3%5C+was%5C+a%5C+little%5C+higher%5C+than%5C+those%5C+of%5C+others.%5C+The%5C+seeds%5C+in%5C+perlite%5C+had%5C+the%5C+highest%5C+germination%5C+percentage%5C+than%5C+those%5C+in%5C+other%5C+substrates."},{"jsname":"the 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&rpp=10&accurate=false&advanced=false&sort_by=2&isNonaffiliated=false&search_type=-1&query1=%25E5%2588%2586%25E5%25AD%2590%25E7%25B3%25BB%25E7%25BB%259F%25E5%25AD%25A6&order=desc&&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":"2024-07-31"}],"资助项目","dc.project.title_filter")'>
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中国杯伞科的系统发育与分类研究
学位论文
: 中国科学院大学, 2022
作者:
何正蜜
Adobe PDF(15394Kb)
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浏览/下载：23/0
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提交时间：2024/05/14
广义杯伞，杯伞科，金钱菌属，单拷贝同源直系基因，毒蕈碱
Clitocybe s.l., Clitocybaceae, Collybia, single-copy gene, muscarine
世界紫堇属（罂粟科）的分子系统学与生物地理学研究
学位论文
: 中国科学院大学, 2022
作者:
陈俊通
Adobe PDF(13289Kb)
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浏览/下载：14/0
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提交时间：2024/05/14
紫堇亚科，紫堇属，系统发育，生物地理，组级新分类系统
Fumarioideae, Corydalis, Phylogeny, Biogeography, New classification
中国罂粟科紫堇属南黄堇组的分类学研究
学位论文
: 中国科学院大学, 2022
作者:
肖金妃
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分类修订，分子系统学，紫堇属，南黄堇组，罂粟科
Taxonomic revision, Molecular phylogenetics, Corydalis, Corydalis sect. Davidianae, Papaveraceae
中国雪花衣属及其近缘属黑川衣属的分类和系统发育研究
学位论文
: 中国科学院大学, 2022
作者:
王禄汀
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提交时间：2024/05/14
雪花衣属，经典分类，系统发育学，新种
Anaptychia, Classical Taxonomy, Phylogeny, New Species
云南薹草属（Carex）分类修订及植物地理学研究
学位论文
: 中国科学院大学, 2022
作者:
李园园
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提交时间：2024/05/14
薹草属，嵩草属，形态学研究，分类修订，植物区系
Carex, Kobresia, Morphological Study, Taxonomic Revision, Flora
叶绿体全基因组序列在香薷属（唇 形科）系统发育中的应用
学位论文
: 中国科学院大学, 2022
作者:
孙增朋
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香薷属
Elsholtzia
叶绿体基因组
Plastomes
系统发育重建
Phylogenetic reconstruction
生物地理学
Biogeography
高变区
Highly variable region
唇形科野芝麻亚科的叶绿体系统发育基因组学研究
学位论文
: 中国科学院大学, 2022
作者:
武忆雯
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提交时间：2024/05/14
野芝麻亚科，刺蕊草族，假野芝麻属，糙苏族，分子系统学
Lamioideae, Pogostemoneae, Paralamium, Phlomideae, molecular phylogenetic study.
大麻科分子系统学研究与分化时间估算
学位论文
, 2021
作者:
付小刚
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浏览/下载：17/0
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提交时间：2024/03/20
被子植物叶绿体系统发育基因组学研究
学位论文
, 2020
作者:
甘露
Adobe PDF(11879Kb)
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浏览/下载：179/1
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提交时间：2023/11/02
滇缅泰地区巨竹属（禾本科：竹亚科）的分类修订
学位论文
, 2020
作者:
许祖昌
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浏览/下载：77/0
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提交时间：2023/11/02
