|
|
|
|
|
|
|
|
|
|
|
|
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 efforts.","jscount":"1","jsurl":"/simple-search?field1=all&field=dc.citation.source_filter&advanced=false&fq=dc.language.iso_filter%3A%E4%B8%AD%E6%96%87&query1=Thaliana&&fq=dc.project.title_filter%3ASophora%5C+davidii%5C+%5C%28Franch.%5C%29%5C+Skeels%5C+is%5C+an%5C+endemic%5C+species%5C+to%5C+China%2C%5C+and%5C+widely%5C+distributed%5C+in%5C+the%5C+dry%5C+valleys%5C+of%5C+the%5C+Himalayan%5C-Hengduan%5C+Mountain%5C+Systems%2C%5C+the%5C+Yungui%5C+Plateau%2C%5C+the%5C+Qinling%5C+Mountain%2C%5C+the%5C+Loess%5C+Plateau%5C+and%5C+other%5C+places%5C+of%5C+China.%5C+Previous%5C+studies%5C+of%5C+plant%5C+phylogeography%5C+have%5C+focused%5C+mainly%5C+on%5C+some%5C+taxa%5C+from%5C+the%5C+mountainous%5C+areas%5C+of%5C+China%2C%5C+relatively%5C+few%5C+studies%5C+have%5C+been%5C+conducted%5C+on%5C+plant%5C+taxa%5C+from%5C+the%5C+river%5C+valleys.%5C+The%5C+population%5C+dynamics%5C+and%5C+evolutionary%5C+history%5C+of%5C+species%5C+in%5C+such%5C+habitat%5C+remain%5C+less%5C+unknown%2C%5C+including%5C+the%5C+factors%5C+affecting%5C+the%5C+population%5C+genetic%5C+structure%5C+and%5C+its%5C+potential%5C+refugia%5C+in%5C+glaciation.%5C+In%5C+this%5C+study%2C%5C+we%5C+first%5C+determine%5C+the%5C+chromosome%5C+number%2C%5C+ploidy%5C+and%5C+karyotype%5C+of%5C+most%5C+populations%5C+we%5C+sampled.%5C+Then%2C%5C+based%5C+on%5C+sequence%5C+data%5C+from%5C+two%5C+maternally%5C+inherited%5C+cpDNA%5C+and%5C+one%5C+biparentally%5C+inherited%5C+nuclear%5C+DNA%5C+fragments%2C%5C+our%5C+study%5C+revealed%5C+the%5C+genetic%5C+diversity%5C+and%5C+population%5C+genetic%5C+structure%5C+of%5C+S.%5C+davidii%5C+and%5C+factors%5C+affecting%5C+them.%5C+The%5C+demographic%5C+history%5C+and%5C+potential%5C+refugia%5C+of%5C+this%5C+speices%5C+were%5C+investigated%5C+and%5C+the%5C+genetic%5C+relationship%5C+among%5C+three%5C+varieties%5C+was%5C+also%5C+clarified.%5C+The%5C+main%5C+results%5C+are%5C+summarized%5C+as%5C+follows%5C%3A1.%5C+Cytogeography%EF%BC%8CThe%5C+chromosome%5C+number%5C+and%5C+karyotypes%5C+of%5C+14%5C+S.%5C+davidii%5C+populations%5C+have%5C+been%5C+studied.%5C+The%5C+results%5C+showed%5C+that%5C+the%5C+choromosome%5C+number%5C+of%5C+all%5C+the%5C+populations%5C+is%5C+2n%5C+%3D%5C+18.%5C+The%5C+interphase%5C+nuclei%5C+and%5C+prophase%5C+chromosomes%5C+of%5C+the%5C+species%5C+were%5C+found%5C+to%5C+be%5C+of%5C+the%5C+complex%5C+chromosome%5C+type%5C+and%5C+interstitial%5C+type.%5C+The%5C+results%5C+of%5C+karyotype%5C+analysis%5C+showed%5C+that%5C+7%5C+of%5C+14%5C+materials%5C+has%5C+satellites%2C%5C+and%5C+the%5C+number%5C+and%5C+position%5C+of%5C+satellites%5C+differ%5C+among%5C+populations%2C%5C+and%5C+thus%5C+revealed%5C+a%5C+series%5C+of%5C+diversified%5C+karyotypes.%5C+With%5C+most%5C+populations%5C+being%5C+of%5C+ploidy%2C%5C+cytogenetical%5C+divergence%5C+within%5C+the%5C+species%5C+lied%5C+mainly%5C+in%5C+chromosome%5C+size%5C+and%5C+structure.%5C+The%5C+fact%5C+that%5C+polyploidization%5C+did%5C+not%5C+occur%5C+very%5C+often%5C+for%5C+variations%5C+in%5C+Southwest%5C+China%5C+was%5C+against%5C+viewpoint%5C+that%5C+polyploidization%5C+level%5C+in%5C+this%5C+area%5C+is%5C+higher%5C+than%5C+that%5C+of%5C+other%5C+distribution%5C+areas%5C+due%5C+to%5C+the%5C+elevation%5C+of%5C+mountains%5C+and%5C+plateau.%5C+2.%5C+Phylogeographic%5C+analysisbased%5C+on%5C+chloroplast%5C+sequence%EF%BC%8CWe%5C+sequenced%5C+two%5C+cpDNA%5C+fragments%5C+rpl32%5C-trnL%5C%28UAG%5C%29intergenic%5C+spacer%5C+and%5C+trnH%5C-psbA%5C+spacer%5C+in%5C+40%5C+populations%5C+sampled%2C%5C+recovering%5C+22%5C+chlorotypes.%5C+The%5C+average%5C+with%5C-in%5C+population%5C+diversity%5C+%5C%28hS%5C+%3D%5C+0.171%5C%29%5C+was%5C+much%5C+lower%5C+than%5C+total%5C+genetic%5C+diversity%5C+%5C%28hT%5C+%3D%5C+0.857%5C%29.%5C+Population%5C+differentiation%5C+was%5C+high%5C+%5C%28NST%5C+%3D%5C+0.924%2C%5C+GST%5C+%3D%5C+0.801%5C%29%5C+indicating%5C+low%5C+levels%5C+of%5C+seed%5C-based%5C+gene%5C+flow%5C+and%5C+significant%5C+phylogeographical%5C+stucture%5C+%5C%28NST%5C+%3E%5C+GST%2C%5C+P%5C+%3C%5C+0.05%5C%29%5C+were%5C+exhibited%5C+by%5C+this%5C+species.%5C+The%5C+SAMOVA%5C+revealed%5C+seven%5C+diverging%5C+groups%5C+of%5C+related%5C+chlorotypes%2C%5C+six%5C+of%5C+them%5C+had%5C+distinct%5C+nonoverlapping%5C+geographical%5C+ranges%5C%3A%5C+one%5C+in%5C+the%5C+northeast%5C+comprising%5C+10%5C+populations%2C%5C+a%5C+second%5C+with%5C+a%5C+southeast%5C+distribution%5C+comprising%5C+22%5C+populations%2C%5C+and%5C+the%5C+remaning%5C+four%5C+groups%5C+comprising%5C+15%5C+populations%5C+located%5C+in%5C+the%5C+west%5C+part%5C+of%5C+the%5C+species%E2%80%99%5C+range%5C+along%5C+different%5C+river%5C+valleys.%5C+The%5C+genetic%5C+clustering%5C+of%5C+populations%5C+into%5C+three%5C+regions%5C+was%5C+also%5C+supported%5C+by%5C+analysis%5C+of%5C+molecular%5C+variance%2C%5C+which%5C+showed%5C+that%5C+most%5C+genetic%5C+variation%5C+%5C%2882.43%25%5C%29%5C+was%5C+found%5C+among%5C+these%5C+three%5C+regions.%5C+Two%5C+clusters%5C+were%5C+distinguished%5C+by%5C+both%5C+phylogenetic%5C+analysis%5C+and%5C+genealogical%5C+analysis%5C+of%5C+chlorotypes%2C%5C+one%5C+consisting%5C+of%5C+chlorotypes%5C+from%5C+the%5C+western%5C+region%5C+and%5C+the%5C+second%5C+consisting%5C+of%5C+those%5C+from%5C+the%5C+eastern%5C+region.%5C+Significant%5C+genetic%5C+differences%5C+between%5C+the%5C+two%5C+regions%5C+might%5C+be%5C+attributed%5C+to%5C+vicariance%5C+and%5C+restricted%5C+gene%5C+flow%2C%5C+and%5C+this%5C+vicariance%5C+could%5C+be%5C+explained%5C+by%5C+the%5C+physical%5C+environmental%5C+heterogeneity%5C+on%5C+each%5C+side%5C+of%5C+the%5C+Tanaka%5C-Kaiyong%5C+Line.%5C+Following%5C+the%5C+uplift%5C+of%5C+the%5C+Tibetan%5C+Plateau%2C%5C+the%5C+reorganization%5C+of%5C+the%5C+major%5C+river%5C+drainages%5C+was%5C+primarily%5C+caused%5C+by%5C+river%5C+separation%5C+and%5C+capture%5C+events.%5C+These%5C+historical%5C+events%5C+could%5C+change%5C+the%5C+distribution%5C+of%5C+S.%5C+davidii%5C+from%5C+fragmented%5C+to%5C+continuous%5C+%5C%28Upper%5C%2FLower%5C+Jinshajiang%5C+and%5C+Yalongjiang%5C%2FDaduhe%5C%29%2C%5C+and%5C+from%5C+continuous%5C+to%5C+fragmented%5C+%5C%28Nujiang%5C+and%5C+Jinshajiang%5C%2FHonghe%5C%29.%5C+However%2C%5C+spatial%5C+and%5C+temporal%5C+patterns%5C+of%5C+phylogeographic%5C+divergence%5C+are%5C+strongly%5C+associated%5C+with%5C+historical%5C+disjunction%5C+rather%5C+than%5C+modern%5C+drainage%5C+connections.%5C+Moreover%2C%5C+the%5C+following%5C+north%5C-south%5C+split%5C+in%5C+the%5C+eastern%5C+region%5C+and%5C+effective%5C+isolation%5C+with%5C+their%5C+genetic%5C+diversity%5C+were%5C+essentially%5C+modelled%5C+by%5C+genetic%5C+drift.%5C+The%5C+higher%5C+chlorotype%5C+richness%5C+and%5C+genetic%5C+divergence%5C+for%5C+populations%5C+in%5C+western%5C+region%5C+compared%5C+with%5C+other%5C+two%5C+regions%5C+suggests%5C+that%5C+there%5C+were%5C+multipe%5C+refugia%5C+or%5C+in%5C+situ%5C+survival%5C+of%5C+S.%5C+davidii%5C+in%5C+the%5C+Himalayan%5C-Hengduan%5C+Mountain%5C+region.%5C+Fixation%5C+of%5C+chlorotypes%5C+in%5C+the%5C+northeastern%5C+region%5C+and%5C+near%5C+fixation%5C+in%5C+the%5C+southeastern%5C+region%5C+suggest%5C+a%5C+recent%5C+colonization%5C+of%5C+these%5C+areas.%5C+We%5C+further%5C+found%5C+that%5C+this%5C+species%5C+underwent%5C+past%5C+range%5C+expansion%5C+around%5C+37%5C-303%5C+thousand%5C+years%5C+ago%5C+%5C%28kya%5C%29.%5C+The%5C+southeastern%5C+populations%5C+likely%5C+experienced%5C+a%5C+demographic%5C+expansion%5C+via%5C+unidirectional%5C+gene%5C+flow%5C+along%5C+rivers%2C%5C+while%5C+northeastern%5C+populations%5C+underwent%5C+a%5C+more%5C+northward%5C+expansion%2C%5C+both%5C+from%5C+initial%5C+populations%5C+%5C%28s%5C%29%5C+%5C%2821%2C%5C+22%2C%5C+23%5C%29%5C+preserved%5C+on%5C+eastern%5C+refugia%5C+%5C%28Jinshajiang%5C%29.%5C+This%5C+process%5C+might%5C+have%5C+been%5C+accompanied%5C+with%5C+a%5C+series%5C+of%5C+founder%5C+effects%5C+or%5C+bottlenecks%5C+making%5C+populations%5C+genetically%5C+impoverished.%5C+3.%5C+Phylogeographic%5C+analysisbased%5C+on%5C+nuclear%5C+sequence%EF%BC%8CWe%5C+sequenced%5C+the%5C+nuclear%5C+%5C%28ncpGS%5C%29%5C+region%5C+in%5C+all%5C+populations%5C+sampled%2C%5C+recovering%5C+23%5C+nuclear%5C+haplotypes.%5C+Compared%5C+to%5C+cpDNA%2C%5C+both%5C+NST%5C+%5C%280.470%5C%29%5C+and%5C+GST%5C+%5C%280.338%5C%29%5C+were%5C+relatively%5C+lower%2C%5C+but%5C+NST%5C+was%5C+also%5C+significantly%5C+larger%5C+than%5C+GST.%5C+37.10%25%5C+of%5C+the%5C+total%5C+variation%5C+was%5C+distributed%5C+among%5C+regions%5C+which%5C+was%5C+much%5C+lower%5C+than%5C+that%5C+shown%5C+by%5C+chlorotypes.%5C+Thus%2C%5C+more%5C+extensive%5C+distribution%5C+of%5C+nuclear%5C+haplotypes%5C+was%5C+exhibited%5C+across%5C+the%5C+geographical%5C+range%5C+instead%5C+of%5C+the%5C+strong%5C+population%5C+subdivision%5C+observed%5C+in%5C+chlorotypes.%5C+Similarly%5C+to%5C+the%5C+chloroplast%5C+data%2C%5C+we%5C+found%5C+that%5C+genetic%5C+differentiation%5C+of%5C+nDNA%5C+was%5C+positively%5C+correlated%5C+with%5C+the%5C+geographical%5C+distance%2C%5C+but%5C+the%5C+increase%5C+in%5C+the%5C+geographical%5C+distance%5C+between%5C+populations%5C+did%5C+not%5C+increase%5C+the%5C+genetic%5C+differentiation%5C+of%5C+nDNA%5C+as%5C+rapidly%5C+as%5C+that%5C+of%5C+cpDNA.%5C+These%5C+contrasting%5C+levels%5C+between%5C+the%5C+chloroplast%5C+and%5C+nuclear%5C+genomes%5C+of%5C+S.%5C+davidii%5C+are%5C+likely%5C+due%5C+to%5C+limited%5C+gene%5C+flow%5C+of%5C+cpDNA%5C+by%5C+seeds%5C+vs.%5C+the%5C+extensive%5C+gene%5C+flow%5C+of%5C+nDNA%5C+by%5C+wind%5C-mediated%5C+pollen%5C+in%5C+the%5C+population%5C+history.%5C+We%5C+also%5C+determined%5C+from%5C+nuclear%5C+markers%5C+that%5C+haplotype%5C+diversity%5C+was%5C+reduced%5C+in%5C+the%5C+southeastern%5C+and%5C+northeastern%5C+regions%5C+due%5C+to%5C+the%5C+loss%5C+of%5C+rare%5C+haplotypes%5C+in%5C+western%5C+region.%5C+This%5C+reduction%5C+of%5C+gene%5C+diversity%5C+is%5C+also%5C+a%5C+signature%5C+of%5C+founder%5C+events%5C+or%5C+recent%5C+bottleneck%5C+during%5C+post%5C-glacial%5C+colonization.%5C+However%2C%5C+nuclear%5C+diversity%5C+within%5C+populations%5C+remains%5C+high.%5C+This%5C+provides%5C+evidence%5C+that%5C+regionally%5C+pollen%5C+flow%5C+might%5C+be%5C+sufficiently%5C+high%5C+to%5C+blur%5C+the%5C+genetic%5C+identity%5C+of%5C+founder%5C+populations%5C+over%5C+a%5C+reasonably%5C+large%5C+spatial%5C+scale.3.%5C+Relationships%5C+among%5C+three%5C+varieties%EF%BC%8CThe%5C+phylogenetic%5C+analysis%5C+identified%5C+two%5C+phylogroups%5C+of%5C+chlorotypes%2C%5C+corresponding%5C+to%5C+S.%5C+davidii%5C+var.%5C+davidii%5C+and%5C+var.%5C+chuansinesis.%5C+The%5C+former%5C+was%5C+distinguished%5C+by%5C+the%5C+abscence%5C+of%5C+predonminant%5C+nuclear%5C+haplotype%5C+H1%5C+of%5C+the%5C+latter.%5C+The%5C+monophyletic%5C+group%5C+of%5C+chlorotypes%5C+in%5C+var.%5C+davidii%5C+and%5C+var.%5C+liangshanesis%5C+showed%5C+their%5C+relatively%5C+close%5C+relationship.%5C+And%5C+their%5C+genetic%5C+divergence%5C+from%5C+the%5C+third%5C+variety%5C+appears%5C+to%5C+be%5C+relative%5C+to%5C+their%5C+slight%5C+morphological%5C+difference%5C+in%5C+leaf%5C+size%5C+and%5C+the%5C+divergent%5C+environmental%5C+niche%5C+spaces%5C+they%5C+occupy.%5C+Thus%2C%5C+the%5C+observed%5C+differences%5C+in%5C+morphological%5C+characters%5C+between%5C+var.%5C+chuansinesis%5C+and%5C+other%5C+two%5C+varieties%5C+can%5C+be%5C+explained%5C+by%5C+the%5C+seed%5C+dispersal%5C+limitation%5C+illustrated%5C+above%5C+%5C%28as%5C+inferred%5C+by%5C+geographical%5C+separation%5C%29%5C+and%5C+by%5C+environmental%5C+heterogeneity%5C+%5C%28as%5C+inferred%5C+by%5C+precipitation%5C+or%5C+elevation%5C%29%5C+or%5C+by%5C+a%5C+combination%5C+of%5C+both.%5C+After%5C+all%2C%5C+the%5C+geological%5C+changes%2C%5C+drainage%5C+reorganization%2C%5C+and%5C+floristic%5C+differences%5C+following%5C+the%5C+Himalayan%5C+uplift%5C+have%5C+been%5C+suggested%5C+to%5C+affect%5C+the%5C+genetic%5C+structure%5C+of%5C+S.%5C+davidii.%5C+These%5C+results%5C+provide%5C+new%5C+insights%5C+into%5C+the%5C+phylogeographic%5C+pattern%5C+of%5C+plants%5C+in%5C+China.%5C+In%5C+addition%2C%5C+the%5C+unique%5C+population%5C+genetic%5C+structure%5C+found%5C+in%5C+S.%5C+davidii%5C+has%5C+provided%5C+important%5C+insights%5C+into%5C+the%5C+evolutionary%5C+history%5C+of%5C+this%5C+species.%5C+The%5C+genetic%5C+profile%5C+uncovered%5C+in%5C+this%5C+study%5C+is%5C+also%5C+critical%5C+for%5C+its%5C+conservation%5C+management.%5C+Our%5C+study%5C+has%5C+uncovered%5C+the%5C+existence%5C+of%5C+at%5C+least%5C+two%5C+%E2%80%98evolutionary%5C+significant%5C+units%E2%80%99%5C+independent%5C+units%5C+within%5C+S.%5C+davidii%2C%5C+corresponding%5C+to%5C+var.%5C+davidii%5C+from%5C+eastern%5C+region%5C+and%5C+var.%5C+chuansinensis%5C+from%5C+western%5C+region.%5C+The%5C+conservation%5C+efforts%5C+should%5C+first%5C+focus%5C+on%5C+most%5C+western%5C+populations%5C+and%5C+on%5C+the%5C+southeastern%5C+ones%5C+exhibiting%5C+high%5C+levels%5C+of%5C+genetic%5C+diversity%2C%5C+while%5C+the%5C+genetically%5C+homogeneous%5C+northeastern%5C+populations%5C+located%5C+in%5C+the%5C+degraded%5C+Loess%5C+Plateau%5C+should%5C+require%5C+much%5C+greater%5C+conservation%5C+efforts."},{"jsname":"The membrane system of cell performs many important functions, such as separates cells from the environment, keeps the biochemical reactions in order ect.. The integrity of membrane is very important for plants to survive, especially under the environmental stress. Among all environmental factors, temperature has the closest relationship with membrane and intensively study on this area has been reported. Most researches are mainly focused on the relationship between the composition of fatty acid about membrane and low temperature, while that with high temperature are rare. Nowadays, the increasing concentration of CO2 resulted in increasing temperature and high temperature has become an important inhibition to crop productivity. Thus, it’s necessary and emergent to study the relationship between membrane lipids and high temperature.In the present dissertation, Arabidopsis and its high temperature sensitive mutant were chosen to study the relationship between membrane lipids and high temperature. The ESI-MS/MS was used to examine the composition of membrane lipids. High temperature includes two categories, one is heat stress and the other is moderate heat stress. Heat stress can be divided into two processes: with and without heat acclimation. Five results have been obtained grounding on these works. Firstly, different change models of membrane lipids during heat stress and moderate stress had been found. The degradation of membrane lipids during moderate heat stress was controlled, while that of heat stress was out of control. During moderate heat stress, the degradation mainly happened on chloroplast, such as DGDG and PG, especially those lipids which has polyunsaturated fatty acids. Under heat stress, the degradation about plasma membrane and chloroplast membrane shared same rates. Secondly, the degradation of membrane lipids was reduced when plants had experienced heat acclimation before heat stress, and this change had nothing to do with accumulation of HSP101. The results suggested the acquired thermo-tolerance not only had related with HSP101, but also with membrane lipids. Thirdly, the amount of phosphatidic acid (PA) played an important role during heat stress. If the amount of PA rose to proper extent, it benefited the plants, while if it rose to high level, it destroyed the membrane structure. At last, the HSP101 mutant had higher ratio of polyunsaturated fatty acids/ saturated fatty acids than that of wild Arabidopsis under long term moderate heat stress. The dissertation also included other two parts: the drought-tolerance of Thellungiella halophila and the chemical structure and bioactivity of the second metabolites from endophytes, which were isolated from Trewia nudiflor. Thellungiella halophila shared the same characteristic with Arabidopsis in many aspects, such as dwarf phenotype, short life cycle, fertility and small genome. The research indicated that at cDNA level, they were also very similar. Besides these Thellungiella halophila was more tolerant to stress condition. The previous research about Thellungiella halophila mainly focused on the high-salinity stress, and the researches of drought stress were rare. In this dissertation we focused on the drought-resistance of Thellungiella halophila. Compare to Arabidopsis, Thellungiella halophila could keep water content in high level, more resist to ROS, good photosynthesis activity and keep the membrane system integrity under drought stress. It was interesting that the substances, which rose when Arabidopsis under stress, were at high level in normal Thellungiella halophila, such as: proline, ABA. The degradation of membrane lipids mainly happened on chloroplast membrane of Arabidopsis. In contrast, the membrane of Thellungiella halophila didn’t change. All these evidence indicated that Thellungiella halophila was more drought-tolerant than Arabidopsis. During the research about the chemical structure and bioactivity of the second metabolites from endophytes, which were isolated from Trewia nudiflor, we isolated 46 endophytes from different parts of plants . 34 species of them were selected for bioactivity test, and the bioactivity test show that 50% of them have some bioactivity. We also isolated 24 compounds from 6 endophytes, and 22 of them have been identified by spectra data, including: macrolides, azaphilones, anthraquinones, and steroids. 8 of them are novel compounds. Judging from results, we know the Trewia nudiflor is good resources to isolate endophytes and the endophytes are good resources to search for novel and bioactivity compounds.","jscount":"1","jsurl":"/simple-search?field1=all&field=dc.citation.source_filter&advanced=false&fq=dc.language.iso_filter%3A%E4%B8%AD%E6%96%87&query1=Thaliana&&fq=dc.project.title_filter%3AThe%5C+membrane%5C+system%5C+of%5C+cell%5C+performs%5C+many%5C+important%5C+functions%2C%5C+such%5C+as%5C+separates%5C+cells%5C+from%5C+the%5C+environment%2C%5C+keeps%5C+the%5C+biochemical%5C+reactions%5C+in%5C+order%5C+ect..%5C+The%5C+integrity%5C+of%5C+membrane%5C+is%5C+very%5C+important%5C+for%5C+plants%5C+to%5C+survive%2C%5C+especially%5C+under%5C+the%5C+environmental%5C+stress.%5C+Among%5C+all%5C+environmental%5C+factors%2C%5C+temperature%5C+has%5C+the%5C+closest%5C+relationship%5C+with%5C+membrane%5C+and%5C+intensively%5C+study%5C+on%5C+this%5C+area%5C+has%5C+been%5C+reported.%5C+Most%5C+researches%5C+are%5C+mainly%5C+focused%5C+on%5C+the%5C+relationship%5C+between%5C+the%5C+composition%5C+of%5C+fatty%5C+acid%5C+about%5C+membrane%5C+and%5C+low%5C+temperature%2C%5C+while%5C+that%5C+with%5C+high%5C+temperature%5C+are%5C+rare.%5C+Nowadays%2C%5C+the%5C+increasing%5C+concentration%5C+of%5C+CO2%5C+resulted%5C+in%5C+increasing%5C+temperature%5C+and%5C+high%5C+temperature%5C+has%5C+become%5C+an%5C+important%5C+inhibition%5C+to%5C+crop%5C+productivity.%5C+Thus%2C%5C+it%E2%80%99s%5C+necessary%5C+and%5C+emergent%5C+to%5C+study%5C+the%5C+relationship%5C+between%5C+membrane%5C+lipids%5C+and%5C+high%5C+temperature.In%5C+the%5C+present%5C+dissertation%2C%5C+Arabidopsis%5C+and%5C+its%5C+high%5C+temperature%5C+sensitive%5C+mutant%5C+were%5C+chosen%5C+to%5C+study%5C+the%5C+relationship%5C+between%5C+membrane%5C+lipids%5C+and%5C+high%5C+temperature.%5C+The%5C+ESI%5C-MS%5C%2FMS%5C+was%5C+used%5C+to%5C+examine%5C+the%5C+composition%5C+of%5C+membrane%5C+lipids.%5C+High%5C+temperature%5C+includes%5C+two%5C+categories%2C%5C+one%5C+is%5C+heat%5C+stress%5C+and%5C+the%5C+other%5C+is%5C+moderate%5C+heat%5C+stress.%5C+Heat%5C+stress%5C+can%5C+be%5C+divided%5C+into%5C+two%5C+processes%5C%3A%5C+with%5C+and%5C+without%5C+heat%5C+acclimation.%5C+Five%5C+results%5C+have%5C+been%5C+obtained%5C+grounding%5C+on%5C+these%5C+works.%5C+Firstly%2C%5C+different%5C+change%5C+models%5C+of%5C+membrane%5C+lipids%5C+during%5C+heat%5C+stress%5C+and%5C+moderate%5C+stress%5C+had%5C+been%5C+found.%5C+The%5C+degradation%5C+of%5C+membrane%5C+lipids%5C+during%5C+moderate%5C+heat%5C+stress%5C+was%5C+controlled%2C%5C+while%5C+that%5C+of%5C+heat%5C+stress%5C+was%5C+out%5C+of%5C+control.%5C+During%5C+moderate%5C+heat%5C+stress%2C%5C+the%5C+degradation%5C+mainly%5C+happened%5C+on%5C+chloroplast%2C%5C+such%5C+as%5C+DGDG%5C+and%5C+PG%2C%5C+especially%5C+those%5C+lipids%5C+which%5C+has%5C+polyunsaturated%5C+fatty%5C+acids.%5C+Under%5C+heat%5C+stress%2C%5C+the%5C+degradation%5C+about%5C+plasma%5C+membrane%5C+and%5C+chloroplast%5C+membrane%5C+shared%5C+same%5C+rates.%5C+Secondly%2C%5C+the%5C+degradation%5C+of%5C+membrane%5C+lipids%5C+was%5C+reduced%5C+when%5C+plants%5C+had%5C+experienced%5C+heat%5C+acclimation%5C+before%5C+heat%5C+stress%2C%5C+and%5C+this%5C+change%5C+had%5C+nothing%5C+to%5C+do%5C+with%5C+accumulation%5C+of%5C+HSP101.%5C+The%5C+results%5C+suggested%5C+the%5C+acquired%5C+thermo%5C-tolerance%5C+not%5C+only%5C+had%5C+related%5C+with%5C+HSP101%2C%5C+but%5C+also%5C+with%5C+membrane%5C+lipids.%5C+Thirdly%2C%5C+the%5C+amount%5C+of%5C+phosphatidic%5C+acid%5C+%5C%28PA%5C%29%5C+played%5C+an%5C+important%5C+role%5C+during%5C+heat%5C+stress.%5C+If%5C+the%5C+amount%5C+of%5C+PA%5C+rose%5C+to%5C+proper%5C+extent%2C%5C+it%5C+benefited%5C+the%5C+plants%2C%5C+while%5C+if%5C+it%5C+rose%5C+to%5C+high%5C+level%2C%5C+it%5C+destroyed%5C+the%5C+membrane%5C+structure.%5C+At%5C+last%2C%5C+the%5C+HSP101%5C+mutant%5C+had%5C+higher%5C+ratio%5C+of%5C+polyunsaturated%5C+fatty%5C+acids%5C%2F%5C+saturated%5C+fatty%5C+acids%5C+than%5C+that%5C+of%5C+wild%5C+Arabidopsis%5C+under%5C+long%5C+term%5C+moderate%5C+heat%5C+stress.%5C+The%5C+dissertation%5C+also%5C+included%5C+other%5C+two%5C+parts%5C%3A%5C+the%5C+drought%5C-tolerance%5C+of%5C+Thellungiella%5C+halophila%5C+and%5C+the%5C+chemical%5C+structure%5C+and%5C+bioactivity%5C+of%5C+the%5C+second%5C+metabolites%5C+from%5C+endophytes%2C%5C+which%5C+were%5C+isolated%5C+from%5C+Trewia%5C+nudiflor.%5C+Thellungiella%5C+halophila%5C+shared%5C+the%5C+same%5C+characteristic%5C+with%5C+Arabidopsis%5C+in%5C+many%5C+aspects%2C%5C+such%5C+as%5C+dwarf%5C+phenotype%2C%5C+short%5C+life%5C+cycle%2C%5C+fertility%5C+and%5C+small%5C+genome.%5C+The%5C+research%5C+indicated%5C+that%5C+at%5C+cDNA%5C+level%2C%5C+they%5C+were%5C+also%5C+very%5C+similar.%5C+Besides%5C+these%5C+Thellungiella%5C+halophila%5C+was%5C+more%5C+tolerant%5C+to%5C+stress%5C+condition.%5C+The%5C+previous%5C+research%5C+about%5C+Thellungiella%5C+halophila%5C+mainly%5C+focused%5C+on%5C+the%5C+high%5C-salinity%5C+stress%2C%5C+and%5C+the%5C+researches%5C+of%5C+drought%5C+stress%5C+were%5C+rare.%5C+In%5C+this%5C+dissertation%5C+we%5C+focused%5C+on%5C+the%5C+drought%5C-resistance%5C+of%5C+Thellungiella%5C+halophila.%5C+Compare%5C+to%5C+Arabidopsis%2C%5C+Thellungiella%5C+halophila%5C+could%5C+keep%5C+water%5C+content%5C+in%5C+high%5C+level%2C%5C+more%5C+resist%5C+to%5C+ROS%2C%5C+good%5C+photosynthesis%5C+activity%5C+and%5C+keep%5C+the%5C+membrane%5C+system%5C+integrity%5C+under%5C+drought%5C+stress.%5C+It%5C+was%5C+interesting%5C+that%5C+the%5C+substances%2C%5C+which%5C+rose%5C+when%5C+Arabidopsis%5C+under%5C+stress%2C%5C+were%5C+at%5C+high%5C+level%5C+in%5C+normal%5C+Thellungiella%5C+halophila%2C%5C+such%5C+as%5C%3A%5C+proline%2C%5C+ABA.%5C+The%5C+degradation%5C+of%5C+membrane%5C+lipids%5C+mainly%5C+happened%5C+on%5C+chloroplast%5C+membrane%5C+of%5C+Arabidopsis.%5C+In%5C+contrast%2C%5C+the%5C+membrane%5C+of%5C+Thellungiella%5C+halophila%5C+didn%E2%80%99t%5C+change.%5C+All%5C+these%5C+evidence%5C+indicated%5C+that%5C+Thellungiella%5C+halophila%5C+was%5C+more%5C+drought%5C-tolerant%5C+than%5C+Arabidopsis.%5C+During%5C+the%5C+research%5C+about%5C+the%5C+chemical%5C+structure%5C+and%5C+bioactivity%5C+of%5C+the%5C+second%5C+metabolites%5C+from%5C+endophytes%2C%5C+which%5C+were%5C+isolated%5C+from%5C+Trewia%5C+nudiflor%2C%5C+we%5C+isolated%5C+46%5C+endophytes%5C+from%5C+different%5C+parts%5C+of%5C+plants%5C+.%5C+34%5C+species%5C+of%5C+them%5C+were%5C+selected%5C+for%5C+bioactivity%5C+test%2C%5C+and%5C+the%5C+bioactivity%5C+test%5C+show%5C+that%5C+50%25%5C+of%5C+them%5C+have%5C+some%5C+bioactivity.%5C+We%5C+also%5C+isolated%5C+24%5C+compounds%5C+from%5C+6%5C+endophytes%2C%5C+and%5C+22%5C+of%5C+them%5C+have%5C+been%5C+identified%5C+by%5C+spectra%5C+data%2C%5C+including%5C%3A%5C+macrolides%2C%5C+azaphilones%2C%5C+anthraquinones%2C%5C+and%5C+steroids.%5C+8%5C+of%5C+them%5C+are%5C+novel%5C+compounds.%5C+Judging%5C+from%5C+results%2C%5C+we%5C+know%5C+the%5C+Trewia%5C+nudiflor%5C+is%5C+good%5C+resources%5C+to%5C+isolate%5C+endophytes%5C+and%5C+the%5C+endophytes%5C+are%5C+good%5C+resources%5C+to%5C+search%5C+for%5C+novel%5C+and%5C+bioactivity%5C+compounds."},{"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 species","jscount":"1","jsurl":"/simple-search?field1=all&field=dc.citation.source_filter&advanced=false&fq=dc.language.iso_filter%3A%E4%B8%AD%E6%96%87&query1=Thaliana&&fq=dc.project.title_filter%3AThe%5C+origin%5C+center%5C+and%5C+diversity%5C+center%5C+of%5C+the%5C+genus%5C+Ligularia%5C+were%5C+considered%5C+to%5C+be%5C+central%5C+China%5C+and%5C+Hengduan%5C+Mountains%5C+Region%5C+%5C%28HMR%5C%29%5C+of%5C+China%2C%5C+respectively.%5C+In%5C+this%5C+research%2C%5C+we%5C+studied%5C+the%5C+phylogeographic%5C+pattern%5C+of%5C+L.%5C+hodgsonii%5C+and%5C+L.%5C+tongolensis%2C%5C+which%5C+was%5C+distributed%5C+in%5C+the%5C+origin%5C+center%5C+and%5C+diversity%5C+center%2C%5C+respectively.%5C+We%5C+aimed%5C+to%5C+infer%5C+the%5C+evolutionary%5C+process%5C+of%5C+Ligularia%5C+species.%5C+1.%5C+The%5C+phylogeography%5C+of%5C+L.%5C+hodgsonii%EF%BC%8CHere%2C%5C+we%5C+investigated%5C+the%5C+phylogeographic%5C+history%5C+of%5C+L.%5C+hodgsonii%5C+disjunctively%5C+distributed%5C+in%5C+China%5C+and%5C+Japan.%5C+Two%5C+hundred%5C+and%5C+eighty%5C+individuals%5C+were%5C+collected%5C+from%5C+29%5C+natural%5C+populations%2C%5C+23%5C+located%5C+in%5C+China%5C+and%5C+6%5C+in%5C+Japan.%5C+A%5C+total%5C+of%5C+19%5C+haplotypes%5C+were%5C+identified%5C+with%5C+the%5C+combination%5C+of%5C+three%5C+chloroplast%5C+DNA%5C+%5C%28cpDNA%5C%29%5C+sequences%5C+variations%5C+%5C%28trnQ%5C-5%E2%80%99rps16%2C%5C+trnL%5C-rpl32%5C+and%5C+psbA%5C-trnH%5C%29.%5C+At%5C+the%5C+species%5C+level%2C%5C+a%5C+high%5C+level%5C+of%5C+haplotype%5C+diversity%5C+%5C%28Hd%5C%29%5C+and%C2%A0total%5C+genetic%5C+diversity%5C+%5C%28HT%5C%29%5C+was%5C+detected.%5C+However%2C%5C+the%5C+average%5C+intrapopulation%5C+diversity%5C+%5C%28HS%5C%29%5C+was%5C+very%5C+low.%5C+Consequently%2C%5C+the%5C+population%5C+differentiation%5C%28NST%5C+%3D%5C+0.989%2C%5C+GST%5C+%3D%5C+0.933%5C+%5C%29%5C+was%5C+pronounced%5C+with%5C+a%5C+significant%5C+phylogeographic%5C+structure%5C+%5C%28NST%5C+%3E%5C+GST%2C%5C+p%5C+%3C%5C+0.01%5C%29.%5C+At%5C+the%5C+regional%5C+level%2C%5C+Chinese%5C+and%5C+Japanese%5C+L.%5C+hodgsonii%5C+had%5C+a%5C+similar%5C+estimate%5C+of%5C+genetic%5C+diversity%5C+%5C%28China%5C%3A%5C+Hd%5C+%3D%5C+0.847%2C%5C+HT%5C+%3D%5C+0.869%5C%3B%5C+Japan%5C%3A%5C+Hd%5C+%3D%5C+0.766%2C%5C+HT%5C+%3D%5C+0.867%5C%29.%5C+Populations%5C+from%5C+China%5C+and%5C+Japan%5C+possess%5C+unique%5C+sets%5C+of%5C+haplotypes%2C%5C+and%5C+no%5C+haplotypes%5C+were%5C+shared%5C+between%5C+the%5C+regions.%5C+Furthermore%2C%5C+both%5C+the%5C+phyloegenetic%5C+and%5C+network%5C+analyses%5C+recovered%5C+the%5C+haplotypes%5C+of%5C+China%5C+and%5C+Japan%5C+as%5C+two%5C+distinct%5C+clades.%5C+Thus%2C%5C+we%5C+suggested%5C+the%5C+disjunct%5C+distribution%5C+of%5C+L.%5C+hodgsonii%5C+in%5C+China%5C+and%5C+Japan%5C+may%5C+present%5C+the%5C+climatic%5C+vicariant%5C+relicts%5C+of%5C+the%5C+ancient%5C+widely%5C+distributed%5C+populations.%5C+After%5C+divergence%2C%5C+this%5C+species%5C+within%5C+each%5C+region%5C+experienced%5C+independent%5C+evolutionary%5C+process.%5C+In%5C+China%2C%5C+L.%5C+hodgsonii%5C+was%5C+distributed%5C+around%5C+the%5C+Sichuan%5C+Basin.%5C+This%5C+distribution%5C+range%5C+can%5C+be%5C+divided%5C+into%5C+five%5C+regions.%5C+They%5C+were%5C+Jiajin%5C+Mountain%5C+region%2C%5C+E%E2%80%99mei%5C+Mountain%5C+region%2C%5C+Yunnan%5C-Guizhou%5C+Plateau%5C+region%2C%5C+Wushan%5C-Wuling%5C+Mountain%5C+region%5C+and%5C+Qinling%5C+Mountain%5C+region.%5C+Twelve%5C+haplotypes%5C+were%5C+indentified%5C+within%5C+these%5C+regions.%5C+Each%5C+region%5C+had%5C+its%5C+own%5C+specific%5C+haplotypes%2C%5C+which%5C+had%5C+different%5C+ancestry%5C+in%5C+the%5C+network.%5C+We%5C+deduced%5C+that%5C+Chinese%5C+L.%5C+hodgsonii%5C+might%5C+survive%5C+the%5C+LGM%5C+in%5C+multiple%5C+isolated%5C+refugia%5C+around%5C+the%5C+Sichuan%5C+Basin.%5C+In%5C+Japan%2C%5C+L.%5C+hodgsonii%5C+was%5C+disjunctively%5C+distributed%5C+in%5C+northern%5C+Honshu%5C+and%5C+Hokkaido.%5C+Seven%5C+haplotypes%5C+were%5C+identified%5C+within%5C+this%5C+region.%5C+However%2C%5C+the%5C+genetic%5C+diversity%5C+in%5C+Honshu%5C+%5C%28Hd%5C+%3D%5C+0.821%5C%29%5C+was%5C+much%5C+higher%5C+than%5C+that%5C+in%5C+Hokkaido%5C+%5C%28Hd%5C+%3D%5C+0.513%5C%29.%5C+And%5C+all%5C+haplotypes%5C+in%5C+Hokkaido%5C+were%5C+derived%5C+from%5C+Honshu.%5C+This%5C+haplotype%5C+distribution%5C+suggested%5C+that%5C+the%5C+northern%5C+Honshu%5C+could%5C+have%5C+served%5C+as%5C+refuge%5C+in%5C+Japan.%5C+Nested%5C+clade%5C+analysis%5C+%5C%28NCA%5C%29%5C+indicated%5C+multiple%5C+forces%5C+including%5C+the%5C+vicariance%5C+and%5C+long%5C-distance%5C+dispersal%5C+affected%5C+the%5C+disjunctive%5C+distribution%5C+among%5C+populations%5C+of%5C+L.%5C+hodgsonii%5C+in%5C+Japan.2.%5C+The%5C+phylogeography%5C+of%5C+L.%5C+tongolensis%EF%BC%8CLigularia%5C+tongolensis%5C+was%5C+distributed%5C+along%5C+the%5C+Jinshajiang%5C+watershed%2C%5C+Yalongjiang%5C+watershed%5C+and%5C+Wumeng%5C+Mountain.%5C+In%5C+order%5C+to%5C+deduce%5C+the%5C+demographic%5C+history%5C+of%5C+this%5C+species%2C%5C+we%5C+sequenced%5C+two%5C+chloroplast%5C+DNA%5C+%5C%28cpDNA%5C%29%5C+intergenic%5C+spacers%5C+%5C%28trnQ%5C-5%E2%80%99rps16%2C%5C+trnL%5C-rpl32%5C%29%5C+in%5C+140%5C+individuals%5C+from%5C+14%5C+populations%5C+of%5C+three%5C+groups%5C+%5C%28Jinshajiang%5C+vs.%5C+Yalongjiang%5C+vs.%5C+Wumeng%5C%29%5C+within%5C+this%5C+species%5C+range.%5C+High%5C+levels%5C+of%5C+haplotype%5C+diversity%5C+%5C%28Hd%5C+%3D%5C+0.814%5C%29%5C+and%5C+total%5C+genetic%5C+diversity%5C+%5C%28HT%5C+%3D%5C+0.862%5C%29%5C+were%5C+detected%5C+at%5C+the%5C+species%5C+level%2C%5C+based%5C+on%5C+a%5C+total%5C+oftwelve%5C+haplotypes%5C+identified.%5C+However%2C%5C+the%5C+intrapopulation%5C+diversity%5C+%5C%28HS%5C+%3D%5C+0.349%5C%29%5C+was%5C+low%2C%5C+which%5C+led%5C+to%5C+the%5C+high%5C+levels%5C+of%5C+genetic%5C+divergence%5C+%5C%28GST%5C+%3D%5C+0.595%2C%5C+NST%5C+%3D%5C+0.614%2C%5C+FST%5C+%3D%5C+0.597%5C%29.%5C+In%5C+consideration%5C+of%5C+the%5C+speciation%5C+of%5C+L.%5C+tongolensis%5C+resulting%5C+from%5C+the%5C+uplifts%5C+of%5C+the%5C+Qinghai%5C-Tibetan%5C+Plateau%5C+%5C%28QTP%5C%29%2C%5C+we%5C+thought%5C+the%5C+present%5C+genetic%5C+structure%5C+of%5C+L.%5C+tongolensis%5C+was%5C+shaped%5C+by%5C+the%5C+fragmentation%5C+of%5C+ancestral%5C+populations%5C+during%5C+the%5C+courses%5C+of%5C+QTP%5C+uplifts.%5C+This%5C+was%5C+further%5C+supported%5C+by%5C+the%5C+absence%5C+of%5C+IBD%5C+tests%5C+%5C%28r%5C+%3D%5C+%E2%80%930.291%2C%5C+p%5C+%3D%5C+0.964%5C%29%2C%5C+which%5C+suggest%5C+that%5C+the%5C+differentiation%5C+had%5C+not%5C+occurred%5C+in%5C+accordance%5C+with%5C+the%5C+isolation%5C+by%5C+distance%5C+model.%5C+The%5C+genetic%5C+differentiation%5C+in%5C+L.%5C+tongolensis%5C+appears%5C+to%5C+be%5C+associated%5C+with%5C+historical%5C+events.%5C+Meanwhile%2C%5C+H2%5C+and%5C+H5%2C%5C+the%5C+dominant%5C+haplotypes%5C+that%5C+located%5C+on%5C+internal%5C+nodes%5C+and%5C+deviated%5C+from%5C+extinct%5C+ancestral%5C+haplotype%5C+in%5C+the%5C+network%2C%5C+were%5C+detected%5C+to%5C+be%5C+shared%5C+between%5C+Jinshajiang%5C+and%5C+Yalongjiang%5C+groups.%5C+We%5C+deduced%5C+that%5C+ancestral%5C+populations%5C+of%5C+this%5C+species%5C+might%5C+have%5C+had%5C+a%5C+continuous%5C+distribution%5C+range%2C%5C+which%5C+was%5C+then%5C+fragmented%5C+and%5C+isolated%5C+by%5C+the%5C+following%5C+tectonic%5C+events.%5C+Finally%2C%5C+the%5C+ancestral%5C+polymorphism%2C%5C+H2%5C+and%5C+H5%2C%5C+were%5C+randomly%5C+allocated%5C+in%5C+Jinshajiang%5C+watershed%5C+and%5C+Yalongjiang%5C+watershed.%5C+Meanwhile%2C%5C+H5%5C+was%5C+the%5C+dominant%5C+haplotype%5C+in%5C+Jinshajiang%5C+watershed%5C%3B%5C+H7%5C+was%5C+the%5C+domiant%5C+haplotype%5C+in%5C+Yalongjiang%5C+watershed%5C+and%5C+Wumeng%5C+Mountain.%5C+This%5C+haplotype%5C+distribution%5C+pattern%5C+indicated%5C+that%5C+each%5C+group%5C+might%5C+have%5C+served%5C+as%5C+a%5C+refuge%5C+for%5C+L.%5C+tongolensis%5C+during%5C+the%5C+Quaternary%5C+Glaciation.%5C+Postglacial%5C+demographic%5C+expansion%5C+was%5C+supported%5C+by%5C+unimodal%5C+mismatch%5C+distribution%5C+and%5C+star%5C-like%5C+phylogenies%2C%5C+with%5C+expansion%5C+ages%5C+of%5C+274%5C+ka%5C+B.%5C+P.%5C+for%5C+this%5C+species"},{"jsname":"The reaction of transphosphatidylation is which phospholipase D catalyzes hydrolytic cleavage of the terminal phosphate diester bond of glycerophosphatides, transfer the phosphatidyl moiety of a phospholipids to a primary alcohol or water, producing phosphatidyl alcohol or phosphatidic acid (PtdOH). Although this reaction plays important role in regulating physical process in plants and anminals, the pathway involved in and detailed regulation mechanism are still unknown or not clear. There are three factors which can affect transphosphatidylation, substrates, enzymes and products. This paper intended to uncover the physical effect of the reaction in detail by changing two indispensable factors, the type of substrate and the PLDs. This paper consist of three researches, the first one, changing the accept substrate of the reaction aims to study the relationship between the structure of alcohols and the physical effect, to reveal the significance of the reaction; secondly, using genetic methods to regulate the expression of PLDs mediating transphosphatidylation intends to study its roles in regulating senescence; thirdly, reducing mostly PA derived from PLDs by addition 1-Butanol try to study the effect of PLD-derived PA on phosphate starvation. 1. Initial research of the effect of alcohols on the palnt growth. In this study, we study on the effect of alcohols on Arabidopsis seed germination, seeding growth and membrane lipids molecules, the metabolic procees and signaling pathway invoved in plant responding to 1-Butanol. According to the results we observed, the toxicity of alcohols and its polarity is positively correlated; the toxicity of alcohols to plants may be related with the butanoate and propanoate metabolic pathway rather than transphosphatidylation, the increase of free IAA is contributed to the resistance to 1-Butanol for WS ecotype Arabidopsis thaliana. Futhermore, five 1-Butanol insensitive mutants have obtained and the mutant sites has identified. Under the same concentration 1-Butanol stress, the five mutants are in better condition no matter physical and chemical level or cellular levels compared to wild-type Arabidopsis thaliana. It is believed that the five mutants definitely provide direct evidence for us to uncover the mechanism of the toxicity of alcohols to plants. 2. The change pattern of the membrane lipid molecules responding to the phytohormones-promoted detached Arabidopsis leaves and the role of PLDα1 and PLDδ in regulating this process. The reason for PLDα1-antisense mutant and PLDδ-knockout mutant delaying phytohormone-promoted senescence may be PLDα1 and PLDδ are response to the ABA and ethylene sinaling; PLDα1-or PLDδ-derived PA contributes to reactive oxygen species (ROS) accumulation; PLDα1-antisense mutant and PLDδ-knockout mutant have higher level of indole-3-acrtic acid (IAA) and zeatin riboside (ZR) level but lower level of abscisic acid (ABA) and jasmonic acid (JA) compared to wild-type Col and wild-type WS, respectively, which is favorable to retard the phytohormone-promoted detached leaves senescence. 3. Application tert-butanol increase the efficiency of phosphate utilization and absord when the phosphate-limited. The seedinges phosphate-starved or not exposed to 1-Butanol was subjected to lethal stress. However, in low phosphate condition, application of tert-butanol lower anthocyanin accumulation, increase the phosphate levels and the siliques number, in a word, tert-butanol attenuates the symptom of phosphate-starved induced. It is suggested that tert-Butanol can increase the utilization and absord efficiency of the limited phosphate, however, more evidences are needed to prove the mechanism.","jscount":"1","jsurl":"/simple-search?field1=all&field=dc.citation.source_filter&advanced=false&fq=dc.language.iso_filter%3A%E4%B8%AD%E6%96%87&query1=Thaliana&&fq=dc.project.title_filter%3AThe%5C+reaction%5C+of%5C+transphosphatidylation%5C+is%5C+which%5C+phospholipase%5C+D%5C+catalyzes%5C+hydrolytic%5C+cleavage%5C+of%5C+the%5C+terminal%5C+phosphate%5C+diester%5C+bond%5C+of%5C+glycerophosphatides%2C%5C+transfer%5C+the%5C+phosphatidyl%5C+moiety%5C+of%5C+a%5C+phospholipids%5C+to%5C+a%5C+primary%5C+alcohol%5C+or%5C+water%2C%5C+producing%5C+phosphatidyl%5C+alcohol%5C+or%5C+phosphatidic%5C+acid%5C+%5C%28PtdOH%5C%29.%5C+Although%5C+this%5C+reaction%5C+plays%5C+important%5C+role%5C+in%5C+regulating%5C+physical%5C+process%5C+in%5C+plants%5C+and%5C+anminals%2C%5C+the%5C+pathway%5C+involved%5C+in%5C+and%5C+detailed%5C+regulation%5C+mechanism%5C+are%5C+still%5C+unknown%5C+or%5C+not%5C+clear.%5C+There%5C+are%5C+three%5C+factors%5C+which%5C+can%5C+affect%5C+transphosphatidylation%2C%5C+substrates%2C%5C+enzymes%5C+and%5C+products.%5C+This%5C+paper%5C+intended%5C+to%5C+uncover%5C+the%5C+physical%5C+effect%5C+of%5C+the%5C+reaction%5C+in%5C+detail%5C+by%5C+changing%5C+two%5C+indispensable%5C+factors%2C%5C+the%5C+type%5C+of%5C+substrate%5C+and%5C+the%5C+PLDs.%5C+This%5C+paper%5C+consist%5C+of%C2%A0three%5C+researches%2C%5C+the%5C+first%5C+one%2C%5C+changing%5C+the%5C+accept%5C+substrate%5C+of%5C+the%5C+reaction%5C+aims%5C+to%5C+study%5C+the%5C+relationship%5C+between%5C+the%5C+structure%5C+of%5C+alcohols%5C+and%5C+the%5C+physical%5C+effect%2C%5C+to%5C+reveal%5C+the%5C+significance%5C+of%5C+the%5C+reaction%5C%3B%5C+secondly%2C%5C+using%5C+genetic%5C+methods%5C+to%5C+regulate%5C+the%5C+expression%5C+of%5C+PLDs%5C+mediating%5C+transphosphatidylation%5C+intends%5C+to%5C+study%5C+its%5C+roles%5C+in%5C+regulating%5C+senescence%5C%3B%5C+thirdly%2C%5C+reducing%5C+mostly%5C+PA%5C+derived%5C+from%5C+PLDs%5C+by%5C+addition%5C+1%5C-Butanol%5C+try%5C+to%5C+study%5C+the%5C+effect%5C+of%5C+PLD%5C-derived%5C+PA%5C+on%5C+phosphate%5C+starvation.%5C+1.%5C+Initial%5C+research%5C+of%5C+the%5C+effect%5C+of%5C+alcohols%5C+on%5C+the%5C+palnt%5C+growth.%5C+In%5C+this%5C+study%2C%5C+we%5C+study%5C+on%5C+the%5C+effect%5C+of%5C+alcohols%5C+on%5C+Arabidopsis%5C+seed%5C+germination%2C%5C+seeding%5C+growth%5C+and%5C+membrane%5C+lipids%5C+molecules%2C%5C+the%5C+metabolic%5C+procees%5C+and%5C+signaling%5C+pathway%5C+invoved%5C+in%5C+plant%5C+responding%5C+to%5C+1%5C-Butanol.%5C+According%5C+to%5C+the%5C+results%5C+we%5C+observed%2C%5C+the%5C+toxicity%5C+of%5C+alcohols%5C+and%5C+its%5C+polarity%5C+is%5C+positively%5C+correlated%5C%3B%5C+the%5C+toxicity%5C+of%5C+alcohols%5C+to%5C+plants%5C+may%5C+be%5C+related%5C+with%5C+the%5C+butanoate%5C+and%5C+propanoate%5C+metabolic%5C+pathway%5C+rather%5C+than%5C+transphosphatidylation%2C%5C+the%5C+increase%5C+of%5C+free%5C+IAA%5C+is%5C+contributed%5C+to%5C+the%5C+resistance%5C+to%5C+1%5C-Butanol%5C+for%5C+WS%5C+ecotype%5C+Arabidopsis%5C+thaliana.%5C+Futhermore%2C%5C+five%5C+1%5C-Butanol%5C+insensitive%5C+mutants%5C+have%5C+obtained%5C+and%5C+the%5C+mutant%5C+sites%5C+has%5C+identified.%5C+Under%5C+the%5C+same%5C+concentration%5C+1%5C-Butanol%5C+stress%2C%5C+the%5C+five%5C+mutants%5C+are%5C+in%5C+better%5C+condition%5C+no%5C+matter%5C+physical%5C+and%5C+chemical%5C+level%5C+or%5C+cellular%5C+levels%5C+compared%5C+to%5C+wild%5C-type%5C+Arabidopsis%5C+thaliana.%5C+It%5C+is%5C+believed%5C+that%5C+the%5C+five%5C+mutants%5C+definitely%5C+provide%5C+direct%5C+evidence%5C+for%5C+us%5C+to%5C+uncover%5C+the%5C+mechanism%5C+of%5C+the%5C+toxicity%5C+of%5C+alcohols%5C+to%5C+plants.%5C+2.%5C+The%5C+change%5C+pattern%5C+of%5C+the%5C+membrane%5C+lipid%5C+molecules%5C+responding%5C+to%5C+the%5C+phytohormones%5C-promoted%5C+detached%5C+Arabidopsis%5C+leaves%5C+and%5C+the%5C+role%5C+of%5C+PLD%CE%B11%5C+and%5C+PLD%CE%B4%5C+in%5C+regulating%5C+this%5C+process.%5C+The%5C+reason%5C+for%5C+PLD%CE%B11%5C-antisense%5C+mutant%5C+and%5C+PLD%CE%B4%5C-knockout%5C+mutant%5C+delaying%5C+phytohormone%5C-promoted%5C+senescence%5C+may%5C+be%5C+PLD%CE%B11%5C+and%5C+PLD%CE%B4%5C+are%5C+response%5C+to%5C+the%5C+ABA%5C+and%5C+ethylene%5C+sinaling%5C%3B%5C+PLD%CE%B11%5C-or%5C+PLD%CE%B4%5C-derived%5C+PA%5C+contributes%5C+to%5C+reactive%5C+oxygen%5C+species%5C+%5C%28ROS%5C%29%5C+accumulation%5C%3B%5C+PLD%CE%B11%5C-antisense%5C+mutant%5C+and%5C+PLD%CE%B4%5C-knockout%5C+mutant%5C+have%5C+higher%5C+level%5C+of%5C+indole%5C-3%5C-acrtic%5C+acid%5C+%5C%28IAA%5C%29%5C+and%5C+zeatin%5C+riboside%5C+%5C%28ZR%5C%29%5C+level%5C+but%5C+lower%5C+level%5C+of%5C+abscisic%5C+acid%5C+%5C%28ABA%5C%29%5C+and%5C+jasmonic%5C+acid%5C+%5C%28JA%5C%29%5C+compared%5C+to%5C+wild%5C-type%5C+Col%5C+and%5C+wild%5C-type%5C+WS%2C%5C+respectively%2C%5C+which%5C+is%5C+favorable%5C+to%5C+retard%5C+the%5C+phytohormone%5C-promoted%5C+detached%5C+leaves%5C+senescence.%5C+3.%5C+Application%5C+tert%5C-butanol%5C+increase%5C+the%5C+efficiency%5C+of%5C+phosphate%5C+utilization%5C+and%5C+absord%5C+when%5C+the%5C+phosphate%5C-limited.%5C+The%5C+seedinges%5C+phosphate%5C-starved%5C+or%5C+not%5C+exposed%5C+to%5C+1%5C-Butanol%5C+was%5C+subjected%5C+to%5C+lethal%5C+stress.%5C+However%2C%5C+in%5C+low%5C+phosphate%5C+condition%2C%5C+application%5C+of%5C+tert%5C-butanol%5C+lower%5C+anthocyanin%5C+accumulation%2C%5C+increase%5C+the%5C+phosphate%5C+levels%5C+and%5C+the%5C+siliques%5C+number%2C%5C+in%5C+a%5C+word%2C%5C+tert%5C-butanol%5C+attenuates%5C+the%5C+symptom%5C+of%5C+phosphate%5C-starved%5C+induced.%5C+It%5C+is%5C+suggested%5C+that%5C+tert%5C-Butanol%5C+can%5C+increase%5C+the%5C+utilization%5C+and%5C+absord%5C+efficiency%5C+of%5C+the%5C+limited%5C+phosphate%2C%5C+however%2C%5C+more%5C+evidences%5C+are%5C+needed%5C+to%5C+prove%5C+the%5C+mechanism."},{"jsname":"Transposable elements (TEs) have been found to be a significant fraction of eukaryotic genomes. Moreover, they make great contributions to the structure, function and evolution of genomes as well as genes. However, some questions such as the mechanisms of retainment of TEs in the genome and their adaptive evolution have not been fully elucidated so far. In this study, the distributions of 17 TE-gene associations among Oryza species were investigated. In addition, the nucleotide diversity was analysed and neutral tests for the region flanking the TE insertions were performed. Based on the above-observed patterns, evolutionary relationships between species in the AA genome group were discussed. The main results are as follows: For each TE-gene association, PCR and electrophoresis were conducted for a total of 107 strains, belonging to different Oryza species. The patterns of each TE-gene association in different species were obtained. It is our finding that 2 associations distribute through all Oryza species. By contrast, other 15 associations were only observed in some Oryza species. On basis of the above-mentioned results, it is likely that insertion events under study occurred in their common ancestor, and then they dispersed with subsequent divergence of different AA genome species. Our datas strongly support that O. meridionalis is the most basal lineage of AA genome group, instead of O. longistaminata.For several TE-gene associations fixed in populations of ancestor, the nucleotide diversity was estimated and neutral tests for the region flanking the TE insertions between populations with and without TE insertions were performed. No significant result was obtained. It is possible that the fixation of mutations with TE insetion is a random process; alternatively, this process is attributable to nature selection. Since the fixation has finished, it is difficult to detect the signature at the sequence level.","jscount":"1","jsurl":"/simple-search?field1=all&field=dc.citation.source_filter&advanced=false&fq=dc.language.iso_filter%3A%E4%B8%AD%E6%96%87&query1=Thaliana&&fq=dc.project.title_filter%3ATransposable%5C+elements%5C+%5C%28TEs%5C%29%5C+have%5C+been%5C+found%5C+to%5C+be%5C+a%5C+significant%5C+fraction%5C+of%5C+eukaryotic%5C+genomes.%5C+Moreover%2C%5C+they%5C+make%5C+great%5C+contributions%5C+to%5C+the%5C+structure%2C%5C+function%5C+and%5C+evolution%5C+of%5C+genomes%5C+as%5C+well%5C+as%5C+genes.%5C+However%2C%5C+some%5C+questions%5C+such%5C+as%5C+the%5C+mechanisms%5C+of%5C+retainment%5C+of%5C+TEs%5C+in%5C+the%5C+genome%5C+and%5C+their%5C+adaptive%5C+evolution%5C+have%5C+not%5C+been%5C+fully%5C+elucidated%5C+so%5C+far.%5C+In%5C+this%5C+study%2C%5C+the%5C+distributions%5C+of%5C+17%5C+TE%5C-gene%5C+associations%5C+among%5C+Oryza%5C+species%5C+were%5C+investigated.%5C+In%5C+addition%2C%5C+the%5C+nucleotide%5C+diversity%5C+was%5C+analysed%5C+and%5C+neutral%5C+tests%5C+for%5C+the%5C+region%5C+flanking%5C+the%5C+TE%5C+insertions%5C+were%5C+performed.%5C+Based%5C+on%5C+the%5C+above%5C-observed%5C+patterns%2C%5C+evolutionary%5C+relationships%5C+between%5C+species%5C+in%5C+the%5C+AA%5C+genome%5C+group%5C+were%5C+discussed.%5C+The%5C+main%5C+results%5C+are%5C+as%5C+follows%5C%3A%5C+For%5C+each%5C+TE%5C-gene%5C+association%2C%5C+PCR%5C+and%5C+electrophoresis%5C+were%5C+conducted%5C+for%5C+a%5C+total%5C+of%5C+107%5C+strains%2C%5C+belonging%5C+to%5C+different%5C+Oryza%5C+species.%5C+The%5C+patterns%5C+of%5C+each%5C+TE%5C-gene%5C+association%5C+in%5C+different%5C+species%5C+were%5C+obtained.%5C+It%5C+is%5C+our%5C+finding%5C+that%5C+2%5C+associations%5C+distribute%5C+through%5C+all%5C+Oryza%5C+species.%5C+By%5C+contrast%2C%5C+other%5C+15%5C+associations%5C+were%5C+only%5C+observed%5C+in%5C+some%5C+Oryza%5C+species.%5C+On%5C+basis%5C+of%5C+the%5C+above%5C-mentioned%5C+results%2C%5C+it%5C+is%5C+likely%5C+that%5C+insertion%5C+events%5C+under%5C+study%5C+occurred%5C+in%5C+their%5C+common%5C+ancestor%2C%5C+and%5C+then%5C+they%5C+dispersed%5C+with%5C+subsequent%5C+divergence%5C+of%5C+different%5C+AA%5C+genome%5C+species.%5C+Our%5C+datas%5C+strongly%5C+support%5C+that%5C+O.%5C+meridionalis%5C+is%5C+the%5C+most%5C+basal%5C+lineage%5C+of%5C+AA%5C+genome%5C+group%2C%5C+instead%5C+of%5C+O.%5C+longistaminata.For%5C+several%5C+TE%5C-gene%5C+associations%5C+fixed%5C+in%5C+populations%5C+of%5C+ancestor%2C%5C+the%5C+nucleotide%5C+diversity%5C+was%5C+estimated%5C+and%5C+neutral%5C+tests%5C+for%5C+the%5C+region%5C+flanking%5C+the%5C+TE%5C+insertions%5C+between%5C+populations%5C+with%5C+and%5C+without%5C+TE%5C+insertions%5C+were%5C+performed.%5C+No%5C+significant%5C+result%5C+was%5C+obtained.%5C+It%5C+is%5C+possible%5C+that%5C+the%5C+fixation%5C+of%5C+mutations%5C+with%5C+TE%5C+insetion%5C+is%5C+a%5C+random%5C+process%5C%3B%5C+alternatively%2C%5C+this%5C+process%5C+is%5C+attributable%5C+to%5C+nature%5C+selection.%5C+Since%5C+the%5C+fixation%5C+has%5C+finished%2C%5C+it%5C+is%5C+difficult%5C+to%5C+detect%5C+the%5C+signature%5C+at%5C+the%5C+sequence%5C+level."},{"jsname":"Trigonobalanus doichangensis is an endangered plant. In this paper, the megasporogenesis and development of female gametophyte, seed morphological traits and seed germination, seed conservation, micropropagation and acclimatization of this species were studied. Combined with the published results of cytology, molecular genetics and other researches,the mechanisms of extinction, basic biology and technology of germplasm conservation and acclimatization of T. doichangensis were discussed. The main results are summarized as follows:1. Megasporogenesis and development of female gametophyte，Stamens exist under the stigma of T. doichangensis, and the pollen is aborted on the later development stage of pistil, therefore, the pistillate flower in function is hermaphrodite flower in morphology. The ovule is anatropous, bitegmic and crassinucellate. The primary archesporium is hypodermal and single-celled and the sporogenous cell of the nucellus functions directly as a megaspore mother cell which goes meiosis to form a linear tetrad. The chalazal megaspore of the tetrad is functional. The development of embryo sac conforms to the polygonum type. There are six ovules in the ovary of T. doichangensis, and only one develops into a seed in normal fruits. In the process of megasporogenesis and development of female gametophyte, there are several links of abortion, and 93.3% of mature embryo sacs is aborted.2. Morphological characters and germination of seeds，Most of the variation occurred among individual trees within populations in seed morphological traits (length, width and 1000-seed weight) and germination-related indices (germination percentage, germination index and vigor index). In addition, the variation in percentage of well-developed seeds among populations and among individual trees within populations is equal, each accounting for 48%. Each of seed morphological traits has significantly positive correlation with each other (p < 0.01), but they have no significant correlation with percentage of well-developed seeds and germination-related indices. In the same batch of seeds of T. doichangensis, there are light-colored and dark-colored seed coats, and development of light-colored seeds is significantly poorer than that of dark-colored seeds.The sensitivity of seeds to high temperature varys in different stages of seed imbibition. In each stage, heat acclimatization don’t increase germination percentage, germination index and fresh weight of seedlings. If the distilled water is substituted by solution of SA during seed imbibition, seed germination and germination index after heat shock are not significantly different from control, but they are significantly higher than that of other treatments. Moreover, when the seeds are treatmented with SA, the fresh weight of seedlings is significantly higher than that of control and other treatments.3. Seed conservation，Seeds of T. doichangensis belong to orthodox seeds which can tolerate certain level of dehydration. The condition of low temperature and low water content of seeds is conducive to seed conservation.Germination of fresh seeds shows significant variation among populations, howerer, germination of the seeds after storage for one year in room temperature shows no significant variation among populations.High temperature and high relative humidity damages the seeds more severely than high temperature does. In addition, low water content of seeds enable the seeds to be more tolerant to high temperature.The electrical conductivity, dehydrogenase activity and germination percentage have no significant correlation with each other.4. Micropropagation and in vitro conservation，Cotyledonary nodes are a kind of efficient explants. Low salt media are conducive to shoot propagation and root induction.The maximum multiplication rate (20-25 shoots/explant within 4 months) is achieved on quarter-strength Murashige and Skoog (1/4 MS) medium supplemented with 1 mg·L-1 6-benzyladenine (6-BA) and 0.05 mg·L-1 α-naphthaleneacetic acid (NAA).Rooting is promoted by auxins, however, IBA alone or low concentrations of NAA are preferable due to small amount of callus induced. The research has established an efficient protocol for micropropagation of T. doichangensis, and it provides technology support for in vitro conservation of special germplasm of the species.5. Acclimatization，Quercus variabilis, Cyclobalanopsis glaucoides and T. doichangensis belong to the family of Fagaceae, and the natural distribution ranges of the 3 species are decreasing in turn. The research suggests that the ranges of temperature tolerance of the 3 species are decreasing corresponding to their distribution ranges.The high and low semi-lethal temperature of one-year old T. doichangensis is 49.5℃ and -5℃ respectively. It suggests that T. doichangensis has a wide range of basic temperature tolerance. Short-term heat and cold acclimatization cannot expand the range of temperature tolerance. It can be inferred that T. doichangensis may lack induced tolerance to temperature. Under proper conditions, ABA can increase the cold tolerance, and SA can increase the heat tolerance of leaf discs of T. doichangensis.","jscount":"1","jsurl":"/simple-search?field1=all&field=dc.citation.source_filter&advanced=false&fq=dc.language.iso_filter%3A%E4%B8%AD%E6%96%87&query1=Thaliana&&fq=dc.project.title_filter%3ATrigonobalanus%5C+doichangensis%5C+is%5C+an%5C+endangered%5C+plant.%5C+In%5C+this%5C+paper%2C%5C+the%5C+megasporogenesis%5C+and%5C+development%5C+of%5C+female%5C+gametophyte%2C%5C+seed%5C+morphological%5C+traits%5C+and%5C+seed%5C+germination%2C%5C+seed%5C+conservation%2C%5C+micropropagation%5C+and%5C+acclimatization%5C+of%5C+this%5C+species%5C+were%5C+studied.%5C+Combined%5C+with%5C+the%5C+published%5C+results%5C+of%5C+cytology%2C%5C+molecular%5C+genetics%5C+and%5C+other%5C+researches%2Cthe%5C+mechanisms%5C+of%5C+extinction%2C%5C+basic%5C+biology%5C+and%5C+technology%5C+of%5C+germplasm%5C+conservation%5C+and%5C+acclimatization%5C+of%5C+T.%5C+doichangensis%5C+were%5C+discussed.%5C+The%5C+main%5C+results%5C+are%5C+summarized%5C+as%5C+follows%5C%3A1.%5C+Megasporogenesis%5C+and%5C+development%5C+of%5C+female%5C+gametophyte%EF%BC%8CStamens%5C+exist%5C+under%5C+the%5C+stigma%5C+of%5C+T.%5C+doichangensis%2C%5C+and%5C+the%5C+pollen%5C+is%5C+aborted%5C+on%5C+the%5C+later%5C+development%5C+stage%5C+of%5C+pistil%2C%5C+therefore%2C%5C+the%5C+pistillate%5C+flower%5C+in%5C+function%5C+is%5C+hermaphrodite%5C+flower%5C+in%5C+morphology.%5C+The%5C+ovule%5C+is%5C+anatropous%2C%5C+bitegmic%5C+and%5C+crassinucellate.%5C+The%5C+primary%5C+archesporium%5C+is%5C+hypodermal%5C+and%5C+single%5C-celled%5C+and%5C+the%5C+sporogenous%5C+cell%5C+of%5C+the%5C+nucellus%5C+functions%5C+directly%5C+as%5C+a%5C+megaspore%5C+mother%5C+cell%5C+which%5C+goes%5C+meiosis%5C+to%5C+form%5C+a%5C+linear%5C+tetrad.%5C+The%5C+chalazal%5C+megaspore%5C+of%5C+the%5C+tetrad%5C+is%5C+functional.%5C+The%5C+development%5C+of%5C+embryo%5C+sac%5C+conforms%5C+to%5C+the%5C+polygonum%5C+type.%5C+There%5C+are%5C+six%5C+ovules%5C+in%5C+the%5C+ovary%5C+of%5C+T.%5C+doichangensis%2C%5C+and%5C+only%5C+one%5C+develops%5C+into%5C+a%5C+seed%5C+in%5C+normal%5C+fruits.%5C+In%5C+the%5C+process%5C+of%5C+megasporogenesis%5C+and%5C+development%5C+of%5C+female%5C+gametophyte%2C%5C+there%5C+are%5C+several%5C+links%5C+of%5C+abortion%2C%5C+and%5C+93.3%25%5C+of%5C+mature%5C+embryo%5C+sacs%5C+is%5C+aborted.2.%5C+Morphological%5C+characters%5C+and%5C+germination%5C+of%5C+seeds%EF%BC%8CMost%5C+of%5C+the%5C+variation%5C+occurred%5C+among%5C+individual%5C+trees%5C+within%5C+populations%5C+in%5C+seed%5C+morphological%5C+traits%5C+%5C%28length%2C%5C+width%5C+and%5C+1000%5C-seed%5C+weight%5C%29%5C+and%5C+germination%5C-related%5C+indices%5C+%5C%28germination%5C+percentage%2C%5C+germination%5C+index%5C+and%5C+vigor%5C+index%5C%29.%5C+In%5C+addition%2C%5C+the%5C+variation%5C+in%5C+percentage%5C+of%5C+well%5C-developed%5C+seeds%5C+among%5C+populations%5C+and%5C+among%5C+individual%5C+trees%5C+within%5C+populations%5C+is%5C+equal%2C%5C+each%5C+accounting%5C+for%5C+48%25.%5C+Each%5C+of%5C+seed%5C+morphological%5C+traits%5C+has%5C+significantly%5C+positive%5C+correlation%5C+with%5C+each%5C+other%5C+%5C%28p%5C+%3C%5C+0.01%5C%29%2C%5C+but%5C+they%5C+have%5C+no%5C+significant%5C+correlation%5C+with%5C+percentage%5C+of%5C+well%5C-developed%5C+seeds%5C+and%5C+germination%5C-related%5C+indices.%5C+In%5C+the%5C+same%5C+batch%5C+of%5C+seeds%5C+of%5C+T.%5C+doichangensis%2C%5C+there%5C+are%5C+light%5C-colored%5C+and%5C+dark%5C-colored%5C+seed%5C+coats%2C%5C+and%5C+development%5C+of%5C+light%5C-colored%5C+seeds%5C+is%5C+significantly%5C+poorer%5C+than%5C+that%5C+of%5C+dark%5C-colored%5C+seeds.The%5C+sensitivity%5C+of%5C+seeds%5C+to%5C+high%5C+temperature%5C+varys%5C+in%5C+different%5C+stages%5C+of%5C+seed%5C+imbibition.%5C+In%5C+each%5C+stage%2C%5C+heat%5C+acclimatization%5C+don%E2%80%99t%5C+increase%5C+germination%5C+percentage%2C%5C+germination%5C+index%5C+and%5C+fresh%5C+weight%5C+of%5C+seedlings.%5C+If%5C+the%5C+distilled%5C+water%5C+is%5C+substituted%5C+by%5C+solution%5C+of%5C+SA%5C+during%5C+seed%5C+imbibition%2C%5C+seed%5C+germination%5C+and%5C+germination%5C+index%5C+after%5C+heat%5C+shock%5C+are%5C+not%5C+significantly%5C+different%5C+from%5C+control%2C%5C+but%5C+they%5C+are%5C+significantly%5C+higher%5C+than%5C+that%5C+of%5C+other%5C+treatments.%5C+Moreover%2C%5C+when%5C+the%5C+seeds%5C+are%5C+treatmented%5C+with%5C+SA%2C%5C+the%5C+fresh%5C+weight%5C+of%5C+seedlings%5C+is%5C+significantly%5C+higher%5C+than%5C+that%5C+of%5C+control%5C+and%5C+other%5C+treatments.3.%5C+Seed%5C+conservation%EF%BC%8CSeeds%5C+of%5C+T.%5C+doichangensis%5C+belong%5C+to%5C+orthodox%5C+seeds%5C+which%5C+can%5C+tolerate%5C+certain%5C+level%5C+of%5C+dehydration.%5C+The%5C+condition%5C+of%5C+low%5C+temperature%5C+and%5C+low%5C+water%5C+content%5C+of%5C+seeds%5C+is%5C+conducive%5C+to%5C+seed%5C+conservation.Germination%5C+of%5C+fresh%5C+seeds%5C+shows%5C+significant%5C+variation%5C+among%5C+populations%2C%5C+howerer%2C%5C+germination%5C+of%5C+the%5C+seeds%5C+after%5C+storage%5C+for%5C+one%5C+year%5C+in%5C+room%5C+temperature%5C+shows%5C+no%5C+significant%5C+variation%5C+among%5C+populations.High%5C+temperature%5C+and%5C+high%5C+relative%5C+humidity%5C+damages%5C+the%5C+seeds%5C+more%5C+severely%5C+than%5C+high%5C+temperature%5C+does.%5C+In%5C+addition%2C%5C+low%5C+water%5C+content%5C+of%5C+seeds%5C+enable%5C+the%5C+seeds%5C+to%5C+be%5C+more%5C+tolerant%5C+to%5C+high%5C+temperature.The%5C+electrical%5C+conductivity%2C%5C+dehydrogenase%5C+activity%5C+and%5C+germination%5C+percentage%5C+have%5C+no%5C+significant%5C+correlation%5C+with%5C+each%5C+other.4.%5C+Micropropagation%5C+and%5C+in%5C+vitro%5C+conservation%EF%BC%8CCotyledonary%5C+nodes%5C+are%5C+a%5C+kind%5C+of%5C+efficient%5C+explants.%5C+Low%5C+salt%5C+media%5C+are%5C+conducive%5C+to%5C+shoot%5C+propagation%5C+and%5C+root%5C+induction.The%5C+maximum%5C+multiplication%5C+rate%5C+%5C%2820%5C-25%5C+shoots%5C%2Fexplant%5C+within%5C+4%5C+months%5C%29%5C+is%5C+achieved%5C+on%5C+quarter%5C-strength%5C+Murashige%5C+and%5C+Skoog%5C+%5C%281%5C%2F4%5C+MS%5C%29%5C+medium%5C+supplemented%5C+with%5C+1%5C+mg%C2%B7L%5C-1%5C+6%5C-benzyladenine%5C+%5C%286%5C-BA%5C%29%5C+and%5C+0.05%5C+mg%C2%B7L%5C-1%5C+%CE%B1%5C-naphthaleneacetic%5C+acid%5C+%5C%28NAA%5C%29.Rooting%5C+is%5C+promoted%5C+by%5C+auxins%2C%5C+however%2C%5C+IBA%5C+alone%5C+or%5C+low%5C+concentrations%5C+of%5C+NAA%5C+are%5C+preferable%5C+due%5C+to%5C+small%5C+amount%5C+of%5C+callus%5C+induced.%5C+The%5C+research%5C+has%5C+established%5C+an%5C+efficient%5C+protocol%5C+for%5C+micropropagation%5C+of%5C+T.%5C+doichangensis%2C%5C+and%5C+it%5C+provides%5C+technology%5C+support%5C+for%5C+in%5C+vitro%5C+conservation%5C+of%5C+special%5C+germplasm%5C+of%5C+the%5C+species.5.%5C+Acclimatization%EF%BC%8CQuercus%5C+variabilis%2C%5C+Cyclobalanopsis%5C+glaucoides%5C+and%5C+T.%5C+doichangensis%5C+belong%5C+to%5C+the%5C+family%5C+of%5C+Fagaceae%2C%5C+and%5C+the%5C+natural%5C+distribution%5C+ranges%5C+of%5C+the%5C+3%5C+species%5C+are%5C+decreasing%5C+in%5C+turn.%5C+The%5C+research%5C+suggests%5C+that%5C+the%5C+ranges%5C+of%5C+temperature%5C+tolerance%5C+of%5C+the%5C+3%5C+species%5C+are%5C+decreasing%5C+corresponding%5C+to%5C+their%5C+distribution%5C+ranges.The%5C+high%5C+and%5C+low%5C+semi%5C-lethal%5C+temperature%5C+of%5C+one%5C-year%5C+old%5C+T.%5C+doichangensis%5C+is%5C+49.5%E2%84%83%5C+and%5C+%5C-5%E2%84%83%5C+respectively.%5C+It%5C+suggests%5C+that%5C+T.%5C+doichangensis%5C+has%5C+a%5C+wide%5C+range%5C+of%5C+basic%5C+temperature%5C+tolerance.%5C+Short%5C-term%5C+heat%5C+and%5C+cold%5C+acclimatization%5C+cannot%5C+expand%5C+the%5C+range%5C+of%5C+temperature%5C+tolerance.%5C+It%5C+can%5C+be%5C+inferred%5C+that%5C+T.%5C+doichangensis%5C+may%5C+lack%5C+induced%5C+tolerance%5C+to%5C+temperature.%5C+Under%5C+proper%5C+conditions%2C%5C+ABA%5C+can%5C+increase%5C+the%5C+cold%5C+tolerance%2C%5C+and%5C+SA%5C+can%5C+increase%5C+the%5C+heat%5C+tolerance%5C+of%5C+leaf%5C+discs%5C+of%5C+T.%5C+doichangensis."},{"jsname":"Until now, little data about the plant reproductive characters and ecological adaptation have been documented in the species-rich Sino-Himalaya region. Anemone rivularis (Ranunculaceae), mainly occurs in this area, and is of particular interest for its unique flower heliotropic movement and sex allocation strategy. In this study, we investigated the reproductive biology and adaptation mechanism of A. rivularis on the Yulong Snow Mountain Lijiang, northwestern Yunnan. The main results were summarized as follows: 1 Reproductive biology, The mating system, flowering phenology, floral morphology and pollination efficiency were examined in Anemone rivularis. This species is a perennial plant with hermaphroditic flowers, and its inflorescence is an acropetal cyme with protogynous flowers. In contrast to some self-incompatible species reported in Anemone, our results proved that A. rivularis was self-compatible. The seed set under natural pollination was more than 70%, indicating that there was no pollen limitation. Meanwhile, the seed set of artificial-cross-pollinated flowers was significantly higher than that of artificial-self-pollinated flowers, suggesting that the mixed mating system of A. rivularis was based on cross-pollination, and the results also supported a favor of outcrossing reproductive strategy for perennial herbs as some previous reports. Clearly, the reproductive strategy of A. rivularis prefer to cross-pollination in the alpine Sino-Himalayan region, in order to improve the reproductive fitness. 2 Flower heliotropism, The flower heliotropic movement mechanism, influences and adaptive significance were investigated in Anemone rivularis. The results indicated that under natural conditions, a treatment of pistils and stamens removal, flowers of A. rivularis retained accurately sun-tracking behavior through daytime, and the petals were found to close in the evening; but flowers would lose heliotropic movement if tepals were removed, with peduncles keeping a vertical orientation. This indicated that the tepals were crucial for heliotropic behavior. The flower heliotropism of A. rivularis was sensitive to blue light frequencies rather than red frequencies, suggesting that the light signal must be received by tepals, which driving the peduncles to bend due to differential cell elongation along the two sides of peduncle. Furthermore, there was a close relationship between diurnal heliotropic movements and temperature of flower interior in A. rivularis. Flowers with tepals could provide a relatively narrow range of temperatures, in comparison with flowers lacking tepals, in order to maintain reproductive organs in functional floral temperature range. Our study demonstrated that both the development of pistils and stamens and the visiting of insects could benefit from flower heliotropism in A. rivularis.3 Sex allocation, Floral traits, male and female functions, reproductive fitness, and sex allocation hypotheses were assessed in intra-inflorescence of Anemone rivularis. Though the inflorescence showed an acropetal flower-opening sequence as well as in many flowering species (early flowers are proximal and late flowers are distal), it engaged different sex allocation strategy. Our observations documented that the late-opening flowers of each inflorescence produce significantly more ovules and fewer pollen grains compared to early-opening flowers, and the pollen:ovule ratio (P:O) declined obviously from primary flower position to tertiary flower position, suggesting that later flowers would tend to favor female-bias investment. The nature-pollinating seed set among flower positions was constant, and there was no resource trade-off between flower size and sexual organs in this species, and the first-removal treatment did not lead to a significant increase in seed set of flowers in the later position. Thus, early-opening flower may not represent a significant competitor for resources with late-opening flowers on the same inflorescence, suggesting that the pattern of floral design and floral display may be determined prior to flowering and is inalterable by resources during flowering. So the female-biased allocation of distal flowers in A. rivularis may be resulted from the the selection by variation in the mating environment.","jscount":"1","jsurl":"/simple-search?field1=all&field=dc.citation.source_filter&advanced=false&fq=dc.language.iso_filter%3A%E4%B8%AD%E6%96%87&query1=Thaliana&&fq=dc.project.title_filter%3AUntil%5C+now%2C%5C+little%5C+data%5C+about%5C+the%5C+plant%5C+reproductive%5C+characters%5C+and%5C+ecological%5C+adaptation%5C+have%5C+been%5C+documented%5C+in%5C+the%5C+species%5C-rich%5C+Sino%5C-Himalaya%5C+region.%5C+Anemone%5C+rivularis%5C+%5C%28Ranunculaceae%5C%29%2C%5C+mainly%5C+occurs%5C+in%5C+this%5C+area%2C%5C+and%5C+is%5C+of%5C+particular%5C+interest%5C+for%5C+its%5C+unique%5C+flower%5C+heliotropic%5C+movement%5C+and%5C+sex%5C+allocation%5C+strategy.%5C+In%5C+this%5C+study%2C%5C+we%5C+investigated%5C+the%5C+reproductive%5C+biology%5C+and%5C+adaptation%5C+mechanism%5C+of%5C+A.%5C+rivularis%5C+on%5C+the%5C+Yulong%5C+Snow%5C+Mountain%5C+Lijiang%2C%5C+northwestern%5C+Yunnan.%5C+The%5C+main%5C+results%5C+were%5C+summarized%5C+as%5C+follows%5C%3A%5C+1%5C+Reproductive%5C+biology%2C%5C+The%5C+mating%5C+system%2C%5C+flowering%5C+phenology%2C%5C+floral%5C+morphology%5C+and%5C+pollination%5C+efficiency%5C+were%5C+examined%5C+in%5C+Anemone%5C+rivularis.%5C+This%5C+species%5C+is%5C+a%5C+perennial%5C+plant%5C+with%5C+hermaphroditic%5C+flowers%2C%5C+and%5C+its%5C+inflorescence%5C+is%5C+an%5C+acropetal%5C+cyme%5C+with%5C+protogynous%5C+flowers.%5C+In%5C+contrast%5C+to%5C+some%5C+self%5C-incompatible%5C+species%5C+reported%5C+in%5C+Anemone%2C%5C+our%5C+results%5C+proved%5C+that%5C+A.%5C+rivularis%5C+was%5C+self%5C-compatible.%5C+The%5C+seed%5C+set%5C+under%5C+natural%5C+pollination%5C+was%5C+more%5C+than%5C+70%25%2C%5C+indicating%5C+that%5C+there%5C+was%5C+no%5C+pollen%5C+limitation.%5C+Meanwhile%2C%5C+the%5C+seed%5C+set%5C+of%5C+artificial%5C-cross%5C-pollinated%5C+flowers%5C+was%5C+significantly%5C+higher%5C+than%5C+that%5C+of%5C+artificial%5C-self%5C-pollinated%5C+flowers%2C%5C+suggesting%5C+that%5C+the%5C+mixed%5C+mating%5C+system%5C+of%5C+A.%5C+rivularis%5C+was%5C+based%5C+on%5C+cross%5C-pollination%2C%5C+and%5C+the%5C+results%5C+also%5C+supported%5C+a%5C+favor%5C+of%5C+outcrossing%5C+reproductive%5C+strategy%5C+for%5C+perennial%5C+herbs%5C+as%5C+some%5C+previous%5C+reports.%5C+Clearly%2C%5C+the%5C+reproductive%5C+strategy%5C+of%5C+A.%5C+rivularis%5C+prefer%5C+to%5C+cross%5C-pollination%5C+in%5C+the%5C+alpine%5C+Sino%5C-Himalayan%5C+region%2C%5C+in%5C+order%5C+to%5C+improve%5C+the%5C+reproductive%5C+fitness.%5C+2%5C+Flower%5C+heliotropism%2C%5C+The%5C+flower%5C+heliotropic%5C+movement%5C+mechanism%2C%5C+influences%5C+and%5C+adaptive%5C+significance%5C+were%5C+investigated%5C+in%5C+Anemone%5C+rivularis.%5C+The%5C+results%5C+indicated%5C+that%5C+under%5C+natural%5C+conditions%2C%5C+a%5C+treatment%5C+of%5C+pistils%5C+and%5C+stamens%5C+removal%2C%5C+flowers%5C+of%5C+A.%5C+rivularis%5C+retained%5C+accurately%5C+sun%5C-tracking%5C+behavior%5C+through%5C+daytime%2C%5C+and%5C+the%5C+petals%5C+were%5C+found%5C+to%5C+close%5C+in%5C+the%5C+evening%5C%3B%5C+but%5C+flowers%5C+would%5C+lose%5C+heliotropic%5C+movement%5C+if%5C+tepals%5C+were%5C+removed%2C%5C+with%5C+peduncles%5C+keeping%5C+a%5C+vertical%5C+orientation.%5C+This%5C+indicated%5C+that%5C+the%5C+tepals%5C+were%5C+crucial%5C+for%5C+heliotropic%5C+behavior.%5C+The%5C+flower%5C+heliotropism%5C+of%5C+A.%5C+rivularis%5C+was%5C+sensitive%5C+to%5C+blue%5C+light%5C+frequencies%5C+rather%5C+than%5C+red%5C+frequencies%2C%5C+suggesting%5C+that%5C+the%5C+light%5C+signal%5C+must%5C+be%5C+received%5C+by%5C+tepals%2C%5C+which%5C+driving%5C+the%5C+peduncles%5C+to%5C+bend%5C+due%5C+to%5C+differential%5C+cell%5C+elongation%5C+along%5C+the%5C+two%5C+sides%5C+of%5C+peduncle.%5C+Furthermore%2C%5C+there%5C+was%5C+a%5C+close%5C+relationship%5C+between%5C+diurnal%5C+heliotropic%5C+movements%5C+and%5C+temperature%5C+of%5C+flower%5C+interior%5C+in%5C+A.%5C+rivularis.%5C+Flowers%5C+with%5C+tepals%5C+could%5C+provide%5C+a%5C+relatively%5C+narrow%5C+range%5C+of%5C+temperatures%2C%5C+in%5C+comparison%5C+with%5C+flowers%5C+lacking%5C+tepals%2C%5C+in%5C+order%5C+to%5C+maintain%5C+reproductive%5C+organs%5C+in%5C+functional%5C+floral%5C+temperature%5C+range.%5C+Our%5C+study%5C+demonstrated%5C+that%5C+both%5C+the%5C+development%5C+of%5C+pistils%5C+and%5C+stamens%5C+and%5C+the%5C+visiting%5C+of%5C+insects%5C+could%5C+benefit%5C+from%5C+flower%5C+heliotropism%5C+in%5C+A.%5C+rivularis.3%5C+Sex%5C+allocation%2C%5C+Floral%5C+traits%2C%5C+male%5C+and%5C+female%5C+functions%2C%5C+reproductive%5C+fitness%2C%5C+and%5C+sex%5C+allocation%5C+hypotheses%5C+were%5C+assessed%5C+in%5C+intra%5C-inflorescence%5C+of%5C+Anemone%5C+rivularis.%5C+Though%5C+the%5C+inflorescence%5C+showed%5C+an%5C+acropetal%5C+flower%5C-opening%5C+sequence%5C+as%5C+well%5C+as%5C+in%5C+many%5C+flowering%5C+species%5C+%5C%28early%5C+flowers%5C+are%5C+proximal%5C+and%5C+late%5C+flowers%5C+are%5C+distal%5C%29%2C%5C+it%5C+engaged%5C+different%5C+sex%5C+allocation%5C+strategy.%5C+Our%5C+observations%5C+documented%5C+that%5C+the%5C+late%5C-opening%5C+flowers%5C+of%5C+each%5C+inflorescence%5C+produce%5C+significantly%5C+more%5C+ovules%5C+and%5C+fewer%5C+pollen%5C+grains%5C+compared%5C+to%5C+early%5C-opening%5C+flowers%2C%5C+and%5C+the%5C+pollen%5C%3Aovule%5C+ratio%5C+%5C%28P%5C%3AO%5C%29%5C+declined%5C+obviously%5C+from%5C+primary%5C+flower%5C+position%5C+to%5C+tertiary%5C+flower%5C+position%2C%5C+suggesting%5C+that%5C+later%5C+flowers%5C+would%5C+tend%5C+to%5C+favor%5C+female%5C-bias%5C+investment.%5C+The%5C+nature%5C-pollinating%5C+seed%5C+set%5C+among%5C+flower%5C+positions%5C+was%5C+constant%2C%5C+and%5C+there%5C+was%5C+no%5C+resource%5C+trade%5C-off%5C+between%5C+flower%5C+size%5C+and%5C+sexual%5C+organs%5C+in%5C+this%5C+species%2C%5C+and%5C+the%5C+first%5C-removal%5C+treatment%5C+did%5C+not%5C+lead%5C+to%5C+a%5C+significant%5C+increase%5C+in%5C+seed%5C+set%5C+of%5C+flowers%5C+in%5C+the%5C+later%5C+position.%5C+Thus%2C%5C+early%5C-opening%5C+flower%5C+may%5C+not%5C+represent%5C+a%5C+significant%5C+competitor%5C+for%5C+resources%5C+with%5C+late%5C-opening%5C+flowers%5C+on%5C+the%5C+same%5C+inflorescence%2C%5C+suggesting%5C+that%5C+the%5C+pattern%5C+of%5C+floral%5C+design%5C+and%5C+floral%5C+display%5C+may%5C+be%5C+determined%5C+prior%5C+to%5C+flowering%5C+and%5C+is%5C+inalterable%5C+by%5C+resources%5C+during%5C+flowering.%5C+So%5C+the%5C+female%5C-biased%5C+allocation%5C+of%5C+distal%5C+flowers%5C+in%5C+A.%5C+rivularis%5C+may%5C+be%5C+resulted%5C+from%5C+the%5C+the%5C+selection%5C+by%5C+variation%5C+in%5C+the%5C+mating%5C+environment."},{"jsname":"With the industrial production of human development, environmental pollution problems have become more serious. Metal ion pollution, especially pollution of heavy metal ions, through the biological processes of crop uptaking and accumulation, causing a serious threat to food security; by affecting plant growth, resulting in ecological problems. Plants response to metal ion stress has an important scientific significance and application value. In this study, we used Columbia ecotype, mutants of Arabidopsis thaliana and Brassica napus as materials, the first part, by detecting the relationship between the changes of osmotic adjustment and the charge (or the radius) of metal ions in leaves, we explored the mechanisms of plant roots response to metal ion stress, in order to research the plants response to metal ion stress at the plant level; the second part, by detecting the changes of membrane lipid molecules in leaves and roots, we studyed the mechanism of plant cell membrane response to metal ion stress, so as to explore the plants response to metal ion stress at the cell level.The main results of the first part are as below: 1. Metal ion has effects on the surrounding molecules depends on its radius, the charge and the structure of electron shell. According to the periodic table, we selected 16 kinds of metal ions with different ionic charge, radius and electron shell structure in research. The setting of the metal ion stress was water culture system with adding metal ions, and we studyed the plants response to metal ions through the roots of and Arabidopsis thaliana and Brassica napus.We found that as the concentration of metal ion increased, the relative leakage of the leaves also increased; and the metal ion which had bigger radius resulted in bigger 50% relative leakage, such as Ca2+ stresses resulted in the biggest 50% relative leakage, K+, Na+ and Mg2+ as follows; and heavy metal ions such as Cu2+, Cd2+, Zn2+ and Hg2+ resulted in the smallest 50% relative leakage of all; and the 50% relative leakage of scarce metals Ce3+ was between them. The evidence above suggested that the relationship between the stress capacity of metal ions and its radius was inverse, and the charge of metal ions was positive, respectively. Above all, the relationship between the stress capacity of metal ions and their ionic potential (ionic charge / radius) was positive. 2. Plants could accumulate Osmo regulation substances and produce lipid peroxidation product malondialdehyde after stress condition. We found that after the same concentration of alkali metal Li+, Na+ and K+ stressed Arabidopsis thaliana and Brassica napus, Li+ stress induced the most free proline and MDA production, and the ion radius of which is the smallest; and after the same concentration of Na+, Mg2+ and Al3+ stress Arabidopsis thaliana and Brassica napus, Al3+ stress induced the most free proline and MDA production, and the ion charge of which was the most; and after the same concentration of Ca2+, Al3+and Fe3+ stress Arabidopsis thaliana and Brassica napus, Fe3+ stress induced the most free proline and MDA production. The evidence above suggested that the relationship between the capacity of proline accumulation and MDA and its radius was inverse, and the charge of metal ions was positive, respectively. Above all, the the relationship between the stress capacity of metal ions and their ionic potential (ionic charge/radius) was positive. Besides, the relationship between the production of MDA and metal ion was similar. 3. Detached leaves of plants with the metal ion treatment also accumulated proline. However, we found that the proline accumulation in the detached leaves had no relationship with the radius and the ionic charge of metal. This showed that the plants response to metal ions was conducted through the root system, rather than a direct result of cells responsed to osmotic stress. 4. To further verify the plant''s root system could sense the metal ions stress, we damaged the root of the plant to observe that metal ions had effects on the proline accumulation in the case of the injury. And we found that root with heat stress had no effect on the relationship between the metal ions and proline accumulation. However, mechanically cutting the root even part of the root of the plants, then exposured to hydroponic culture with the metal ions 5 day, we found that there was no significant diffierence between them. The evidence above suggested that the plants responsed to metal ions conducted through roots are complex, and how to quantify this effect required our futher experiment. 5. P5CS is the key enzyme in proline biothesis in plants. We compared wild-type and P5CS deficient mutants of Arabidopsis responsed to metal ion stress, and found that compared to Columbia ecotype of Arabidopsis thaliana, knockout mutations of P5CS1 resulted in less free proline production under the same stress condition. This suggested that metal ions induced proline production by increasing its synthesis rather than reducing degradation. The main results of the second part are as below: The main organs sensing the environment is cell membrane, and cells can respond to changes through the changes of membrane lipids composition in the environment. It is a common phenomenon that environmental metal ions have effects on the plants, and how to impact the changes of the lipids is a significant question, and so far, we have no idea about this. In the same stress intensity (the value of 50% relative leakage), we use of lipid genomics approaches, and comparedthe effects of 7 metal ions (Li+,Pb2+,Cu2+,Zn2+,Co2+,Fe3+ and Cd2+) with different ionic radius, charge and the electron shell structure on the cell membrane lipids of aboveground and underground parts of plants. Because of the limited time, we did preliminary analysis from the mass of lipid data. We found that effects of the metal ions on the membrane lipid molecules have a variety of performances. And data analysis is working, two examples were as follows: 1. After Li+,Pb2+,Cu2+,Zn2+ and Co2+stressed Arabidopsis thaliana for 5days, there was no significant changes in Lysophosphlipids of roots, however, the lysophospholipid molecules of leaves increased in different degrees.The evidence above indicated that the mechanisms of roots and leaves responsed to metal ions maybe different, they were direct and indirect process, respectively. 2. Fe3+ and Cd2+ are two metal ions with lager ionic potential. We found that after Fe3+ and Cd2+ stressed Arabidopsis thaliana for 12 hours, the LysoPC in roots increased more than houdred times, but Cd2+ with the same stress intensity (the value of 50% relative leakage) had no effect on the LysoPC, almostly. The evidence above suggested that the mechanisms of membrane lipids responsed to different metal ions different, and this mainly had relationship with the characters of metal ions and so on.","jscount":"1","jsurl":"/simple-search?field1=all&field=dc.citation.source_filter&advanced=false&fq=dc.language.iso_filter%3A%E4%B8%AD%E6%96%87&query1=Thaliana&&fq=dc.project.title_filter%3AWith%5C+the%5C+industrial%5C+production%5C+of%5C+human%5C+development%2C%5C+environmental%5C+pollution%5C+problems%5C+have%5C+become%5C+more%5C+serious.%5C+Metal%5C+ion%5C+pollution%2C%5C+especially%5C+pollution%5C+of%5C+heavy%5C+metal%5C+ions%2C%5C+through%5C+the%5C+biological%5C+processes%5C+of%5C+crop%5C+uptaking%5C+and%5C+accumulation%2C%5C+causing%5C+a%5C+serious%5C+threat%5C+to%5C+food%5C+security%5C%3B%5C+by%5C+affecting%5C+plant%5C+growth%2C%5C+resulting%5C+in%5C+ecological%5C+problems.%5C+Plants%5C+response%5C+to%5C+metal%5C+ion%5C+stress%5C+has%5C+an%5C+important%5C+scientific%5C+significance%5C+and%5C+application%5C+value.%5C+In%5C+this%5C+study%2C%5C+we%5C+used%5C+Columbia%5C+ecotype%2C%5C+mutants%5C+of%5C+Arabidopsis%5C+thaliana%5C+and%5C+Brassica%5C+napus%5C+as%5C+materials%2C%5C+the%5C+first%5C+part%2C%5C+by%5C+detecting%5C+the%5C+relationship%5C+between%5C+the%5C+changes%5C+of%5C+osmotic%5C+adjustment%5C+and%5C+the%5C+charge%5C+%5C%28or%5C+the%5C+radius%5C%29%5C+of%5C+metal%5C+ions%5C+in%5C+leaves%2C%5C+we%5C+explored%5C+the%5C+mechanisms%5C+of%5C+plant%5C+roots%5C+response%5C+to%5C+metal%5C+ion%5C+stress%2C%5C+in%5C+order%5C+to%5C+research%5C+the%5C+plants%5C+response%5C+to%5C+metal%5C+ion%5C+stress%5C+at%5C+the%5C+plant%5C+level%5C%3B%5C+the%5C+second%5C+part%2C%5C+by%5C+detecting%5C+the%5C+changes%5C+of%5C+membrane%5C+lipid%5C+molecules%5C+in%5C+leaves%5C+and%5C+roots%2C%5C+we%5C+studyed%5C+the%5C+mechanism%5C+of%5C+plant%5C+cell%5C+membrane%5C+response%5C+to%5C+metal%5C+ion%5C+stress%2C%5C+so%5C+as%5C+to%5C+explore%5C+the%5C+plants%5C+response%5C+to%5C+metal%5C+ion%5C+stress%5C+at%5C+the%5C+cell%5C+level.The%5C+main%5C+results%5C+of%5C+the%5C+first%5C+part%5C+are%5C+as%5C+below%5C%3A%5C+1.%5C+Metal%5C+ion%5C+has%5C+effects%5C+on%5C+the%5C+surrounding%5C+molecules%5C+depends%5C+on%5C+its%5C+radius%2C%5C+the%5C+charge%5C+and%5C+the%5C+structure%5C+of%5C+electron%5C+shell.%5C+According%5C+to%5C+the%5C+periodic%5C+table%2C%5C+we%5C+selected%5C+16%5C+kinds%5C+of%5C+metal%5C+ions%5C+with%5C+different%5C+ionic%5C+charge%2C%5C+radius%5C+and%5C+electron%5C+shell%5C+structure%5C+in%5C+research.%5C+The%5C+setting%5C+of%5C+the%5C+metal%5C+ion%5C+stress%5C+was%5C+water%5C+culture%5C+system%5C+with%5C+adding%5C+metal%5C+ions%2C%5C+and%5C+we%5C+studyed%5C+the%5C+plants%5C+response%5C+to%5C+metal%5C+ions%5C+through%5C+the%5C+roots%5C+of%5C+and%5C+Arabidopsis%5C+thaliana%5C+and%5C+Brassica%5C+napus.We%5C+found%5C+that%5C+as%5C+the%5C+concentration%5C+of%5C+metal%5C+ion%5C+increased%2C%5C+the%5C+relative%5C+leakage%5C+of%5C+the%5C+leaves%5C+also%5C+increased%5C%3B%5C+and%5C+the%5C+metal%5C+ion%5C+which%5C+had%5C+bigger%5C+radius%5C+resulted%5C+in%5C+bigger%5C+50%25%5C+relative%5C+leakage%2C%5C+such%5C+as%5C+Ca2%5C%2B%5C+stresses%5C+resulted%5C+in%5C+the%5C+biggest%5C+50%25%5C+relative%5C+leakage%2C%5C+K%5C%2B%2C%5C+Na%5C%2B%5C+and%5C+Mg2%5C%2B%5C+as%5C+follows%5C%3B%5C+and%5C+heavy%5C+metal%5C+ions%5C+such%5C+as%5C+Cu2%5C%2B%2C%5C+Cd2%5C%2B%2C%5C+Zn2%5C%2B%5C+and%5C+Hg2%5C%2B%5C+resulted%5C+in%5C+the%5C+smallest%5C+50%25%5C+relative%5C+leakage%5C+of%5C+all%5C%3B%5C+and%5C+the%5C+50%25%5C+relative%5C+leakage%5C+of%5C+scarce%5C+metals%5C+Ce3%5C%2B%5C+was%5C+between%5C+them.%5C+The%5C+evidence%5C+above%5C+suggested%5C+that%5C+the%5C+relationship%5C+between%5C+the%5C+stress%5C+capacity%5C+of%5C+metal%5C+ions%5C+and%5C+its%5C+radius%5C+was%5C+inverse%2C%5C+and%5C+the%5C+charge%5C+of%5C+metal%5C+ions%5C+was%5C+positive%2C%5C+respectively.%5C+Above%5C+all%2C%5C+the%5C+relationship%5C+between%5C+the%5C+stress%5C+capacity%5C+of%5C+metal%5C+ions%5C+and%5C+their%5C+ionic%5C+potential%5C+%5C%28ionic%5C+charge%5C+%5C%2F%5C+radius%5C%29%5C+was%5C+positive.%5C+2.%5C+Plants%5C+could%5C+accumulate%5C+Osmo%5C+regulation%5C+substances%5C+and%5C+produce%5C+lipid%5C+peroxidation%5C+product%5C+malondialdehyde%5C+after%5C+stress%5C+condition.%5C+We%5C+found%5C+that%5C+after%5C+the%5C+same%5C+concentration%5C+of%5C+alkali%5C+metal%5C+Li%5C%2B%2C%5C+Na%5C%2B%5C+and%5C+K%5C%2B%5C+stressed%5C+Arabidopsis%5C+thaliana%5C+and%5C+Brassica%5C+napus%2C%5C+Li%5C%2B%5C+stress%5C+induced%5C+the%5C+most%5C+free%5C+proline%5C+and%5C+MDA%5C+production%2C%5C+and%5C+the%5C+ion%5C+radius%5C+of%5C+which%5C+is%5C+the%5C+smallest%5C%3B%5C+and%5C+after%5C+the%5C+same%5C+concentration%5C+of%5C+Na%5C%2B%2C%5C+Mg2%5C%2B%5C+and%5C+Al3%5C%2B%5C+stress%5C+Arabidopsis%5C+thaliana%5C+and%5C+Brassica%5C+napus%2C%5C+Al3%5C%2B%5C+stress%5C+induced%5C+the%5C+most%5C+free%5C+proline%5C+and%5C+MDA%5C+production%2C%5C+and%5C+the%5C+ion%5C+charge%5C+of%5C+which%5C+was%5C+the%5C+most%5C%3B%5C+and%5C+after%5C+the%5C+same%5C+concentration%5C+of%5C+Ca2%5C%2B%2C%5C+Al3%5C%2Band%5C+Fe3%5C%2B%5C+stress%5C+Arabidopsis%5C+thaliana%5C+and%5C+Brassica%5C+napus%2C%5C+Fe3%5C%2B%5C+stress%5C+induced%5C+the%5C+most%5C+free%5C+proline%5C+and%5C+MDA%5C+production.%5C+The%5C+evidence%5C+above%5C+suggested%5C+that%5C+the%5C+relationship%5C+between%5C+the%5C+capacity%5C+of%5C+proline%5C+accumulation%5C+and%5C+MDA%5C+and%5C+its%5C+radius%5C+was%5C+inverse%2C%5C+and%5C+the%5C+charge%5C+of%5C+metal%5C+ions%5C+was%5C+positive%2C%5C+respectively.%5C+Above%5C+all%2C%5C+the%5C+the%5C+relationship%5C+between%5C+the%5C+stress%5C+capacity%5C+of%5C+metal%5C+ions%5C+and%5C+their%5C+ionic%5C+potential%5C+%5C%28ionic%5C+charge%5C%2Fradius%5C%29%5C+was%5C+positive.%5C+Besides%2C%5C+the%5C+relationship%5C+between%5C+the%5C+production%5C+of%5C+MDA%5C+and%5C+metal%5C+ion%5C+was%5C+similar.%5C+3.%5C+Detached%5C+leaves%5C+of%5C+plants%5C+with%5C+the%5C+metal%5C+ion%5C+treatment%5C+also%5C+accumulated%5C+proline.%5C+However%2C%5C+we%5C+found%5C+that%5C+the%5C+proline%5C+accumulation%5C+in%5C+the%5C+detached%5C+leaves%5C+had%5C+no%5C+relationship%5C+with%5C+the%5C+radius%5C+and%5C+the%5C+ionic%5C+charge%5C+of%5C+metal.%5C+This%5C+showed%5C+that%5C+the%5C+plants%5C+response%5C+to%5C+metal%5C+ions%5C+was%5C+conducted%5C+through%5C+the%5C+root%5C+system%2C%5C+rather%5C+than%5C+a%5C+direct%5C+result%5C+of%5C+cells%5C+responsed%5C+to%5C+osmotic%5C+stress.%5C+4.%5C+To%5C+further%5C+verify%5C+the%5C+plant%27%27s%5C+root%5C+system%5C+could%5C+sense%5C+the%5C+metal%5C+ions%5C+stress%2C%5C+we%5C+damaged%5C+the%5C+root%5C+of%5C+the%5C+plant%5C+to%5C+observe%5C+that%5C+metal%5C+ions%5C+had%5C+effects%5C+on%5C+the%5C+proline%5C+accumulation%5C+in%5C+the%5C+case%5C+of%5C+the%5C+injury.%5C+And%5C+we%5C+found%5C+that%5C+root%5C+with%5C+heat%5C+stress%5C+had%5C+no%5C+effect%5C+on%5C+the%5C+relationship%5C+between%5C+the%5C+metal%5C+ions%5C+and%5C+proline%5C+accumulation.%5C+However%2C%5C+mechanically%5C+cutting%5C+the%5C+root%5C+even%5C+part%5C+of%5C+the%5C+root%5C+of%5C+the%5C+plants%2C%5C+then%5C+exposured%5C+to%5C+hydroponic%5C+culture%5C+with%5C+the%5C+metal%5C+ions%5C+5%5C+day%2C%5C+we%5C+found%5C+that%5C+there%5C+was%5C+no%5C+significant%5C+diffierence%5C+between%5C+them.%5C+The%5C+evidence%5C+above%5C+suggested%5C+that%5C+the%5C+plants%5C+responsed%5C+to%5C+metal%5C+ions%5C+conducted%5C+through%5C+roots%5C+are%5C+complex%2C%5C+and%5C+how%5C+to%5C+quantify%5C+this%5C+effect%5C+required%5C+our%5C+futher%5C+experiment.%5C+5.%5C+P5CS%5C+is%5C+the%5C+key%5C+enzyme%5C+in%5C+proline%5C+biothesis%5C+in%5C+plants.%5C+We%5C+compared%5C+wild%5C-type%5C+and%5C+P5CS%5C+deficient%5C+mutants%5C+of%5C+Arabidopsis%5C+responsed%5C+to%5C+metal%5C+ion%5C+stress%2C%5C+and%5C+found%5C+that%5C+compared%5C+to%5C+Columbia%5C+ecotype%5C+of%5C+Arabidopsis%5C+thaliana%2C%5C+knockout%5C+mutations%5C+of%5C+P5CS1%5C+resulted%5C+in%5C+less%5C+free%5C+proline%5C+production%5C+under%5C+the%5C+same%5C+stress%5C+condition.%5C+This%5C+suggested%5C+that%5C+metal%5C+ions%5C+induced%5C+proline%5C+production%5C+by%5C+increasing%5C+its%5C+synthesis%5C+rather%5C+than%5C+reducing%5C+degradation.%5C+The%5C+main%5C+results%5C+of%5C+the%5C+second%5C+part%5C+are%5C+as%5C+below%5C%3A%5C+The%5C+main%5C+organs%5C+sensing%5C+the%5C+environment%5C+is%5C+cell%5C+membrane%2C%5C+and%5C+cells%5C+can%5C+respond%5C+to%5C+changes%5C+through%5C+the%5C+changes%5C+of%5C+membrane%5C+lipids%5C+composition%5C+in%5C+the%5C+environment.%5C+It%5C+is%5C+a%5C+common%5C+phenomenon%5C+that%5C+environmental%5C+metal%5C+ions%5C+have%5C+effects%5C+on%5C+the%5C+plants%2C%5C+and%5C+how%5C+to%5C+impact%5C+the%5C+changes%5C+of%5C+the%5C+lipids%5C+is%5C+a%5C+significant%5C+question%2C%5C+and%5C+so%5C+far%2C%5C+we%5C+have%5C+no%5C+idea%5C+about%5C+this.%5C+In%5C+the%5C+same%5C+stress%5C+intensity%5C+%5C%28the%5C+value%5C+of%5C+50%25%5C+relative%5C+leakage%5C%29%2C%5C+we%5C+use%5C+of%5C+lipid%5C+genomics%5C+approaches%2C%5C+and%5C+comparedthe%5C+effects%5C+of%5C+7%5C+metal%5C+ions%5C+%5C%28Li%5C%2B%2CPb2%5C%2B%2CCu2%5C%2B%2CZn2%5C%2B%2CCo2%5C%2B%2CFe3%5C%2B%5C+and%5C+Cd2%5C%2B%5C%29%5C+with%5C+different%5C+ionic%5C+radius%2C%5C+charge%5C+and%5C+the%5C+electron%5C+shell%5C+structure%5C+on%5C+the%5C+cell%5C+membrane%5C+lipids%5C+of%5C+aboveground%5C+and%5C+underground%5C+parts%5C+of%5C+plants.%5C+Because%5C+of%5C+the%5C+limited%5C+time%2C%5C+we%5C+did%5C+preliminary%5C+analysis%5C+from%5C+the%5C+mass%5C+of%5C+lipid%5C+data.%5C+We%5C+found%5C+that%5C+effects%5C+of%5C+the%5C+metal%5C+ions%5C+on%5C+the%5C+membrane%5C+lipid%5C+molecules%5C+have%5C+a%5C+variety%5C+of%5C+performances.%5C+And%5C+data%5C+analysis%5C+is%5C+working%2C%5C+two%5C+examples%5C+were%5C+as%5C+follows%5C%3A%5C+1.%5C+After%5C+Li%5C%2B%2CPb2%5C%2B%2CCu2%5C%2B%2CZn2%5C%2B%5C+and%5C+Co2%5C%2Bstressed%5C+Arabidopsis%5C+thaliana%5C+for%5C+5days%2C%5C+there%5C+was%5C+no%5C+significant%5C+changes%5C+in%5C+Lysophosphlipids%5C+of%5C+roots%2C%5C+however%2C%5C+the%5C+lysophospholipid%5C+molecules%5C+of%5C+leaves%5C+increased%5C+in%5C+different%5C+degrees.The%5C+evidence%5C+above%5C+indicated%5C+that%5C+the%5C+mechanisms%5C+of%5C+roots%5C+and%5C+leaves%5C+responsed%5C+to%5C+metal%5C+ions%5C+maybe%5C+different%2C%5C+they%5C+were%5C+direct%5C+and%5C+indirect%5C+process%2C%5C+respectively.%5C+2.%5C+Fe3%5C%2B%5C+and%5C+Cd2%5C%2B%5C+are%5C+two%5C+metal%5C+ions%5C+with%5C+lager%5C+ionic%5C+potential.%5C+We%5C+found%5C+that%5C+after%5C+Fe3%5C%2B%5C+and%5C+Cd2%5C%2B%5C+stressed%5C+Arabidopsis%5C+thaliana%5C+for%5C+12%5C+hours%2C%5C+the%5C+LysoPC%5C+in%5C+roots%5C+increased%5C+more%5C+than%5C+houdred%5C+times%2C%5C+but%5C+Cd2%5C%2B%5C+with%5C+the%5C+same%5C+stress%5C+intensity%5C+%5C%28the%5C+value%5C+of%5C+50%25%5C+relative%5C+leakage%5C%29%5C+had%5C+no%5C+effect%5C+on%5C+the%5C+LysoPC%2C%5C+almostly.%5C+The%5C+evidence%5C+above%5C+suggested%5C+that%5C+the%5C+mechanisms%5C+of%5C+membrane%5C+lipids%5C+responsed%5C+to%5C+different%5C+metal%5C+ions%5C+different%2C%5C+and%5C+this%5C+mainly%5C+had%5C+relationship%5C+with%5C+the%5C+characters%5C+of%5C+metal%5C+ions%5C+and%5C+so%5C+on."},{"jsname":"项目2","jscount":"1","jsurl":"/simple-search?field1=all&field=dc.citation.source_filter&advanced=false&fq=dc.language.iso_filter%3A%E4%B8%AD%E6%96%87&query1=Thaliana&&fq=dc.project.title_filter%3A%E9%A1%B9%E7%9B%AE2"},{"jsname":"lastIndexed","jscount":"2024-09-19"}],"资助项目","dc.project.title_filter")'>
|
|
|
|
|
