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中国科学院昆明植物研究所知识管理系统
Knowledge Management System of Kunming Institute of Botany,CAS
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GST,p < 0.001) and low levels of seed-based gene flow. C. debaoensis (Cycadaceae) is an endangered species restricted to the border of Guangxi and Yunnan province in southwest China. This species has been classified into two types: sand and karst, according to the soil matrix they grow on. We examined chloroplast sequence variation of the cpDNA sequences from 11 populations of this species. Significant population genetic differentiation was detected (GST= 0.684 and FST = 0.74160). There was marked genetic differentiation between populations in the sand and karst regions and no expansion was detected. Climate changes during glacial periods have had significant effects on the current distribution of cycads. The molecular phylogenetic data, together with the geographic distribution of the haplotypes, suggest that C. debaoensis experienced range contraction during glacial periods, and that the current populations are still confined to the original refugia in southwest China which have favorable habitats in glacial period. These results imply that small refugia were maintained in both sand and karst regions during the LGM (last glacial maximum). This species had no postglacial recolonization and only stayed in these refugia up to now. The low within-population diversity of C. debaoensis suggests that there were strong bottleneck events or founder effects within each separate region during the Quaternary climatic oscillations. Relatively high genetic and haplotype diversities were detected in the newly discovered populations, which located at intermediate locality of sand regions and had morphological variation; this is probably the consequence of the admixture of different haplotypes colonizing the area from separate sources. C. micholitzii occurs in the Annan Highlands in central Vietnam near the Laos border. C. bifida occurs in North Vietnam; its distribution extends across the border into adjacent localities in Guangxi and Yunnan in China. For the comparability between them,theywere considered as the same species C. micholitzii by many academicians. The cpDNA sequences from 11 populations showed that these very controversial species, C. micholitzii and C. bifida, is paraphyletic and should belong to the same species C. micholitzii. AMOVA analysis showed that the component of among-population within region/species (76.46%) was unexpectedly larger than the among-species/region component (14.97%), which also indicates that there is no justification for recognizing two species as C. micholitzii and C. bifida. This hypothesis was also supported by the geological data, especially the neotectonic history of the indo-china block, which started to move south since Oligocene and cause the geographic isolation of these two groups. Therefore, the most likely explanation to the phenotypic similarities between these two groups may be the retention of ancestral polymorphisms in the paraphyletic group due to incomplete lineage sorting. Furthermore, the similarities may also be ascribed to pollen-mediated gene flow among geographically proximate populations and/or phenotypic convergence under similar selection schemes in the same region. C.micholitzi had the higest genetic diversity (HT = 0.980,) and genetic differentiation (GST = 0.830, NST = 0.915) among the C. micholitzii complex. The high genetic diversity might be attributed to its long evolutionary history, highly diverse habitats. The ineffective mode of seed dispersal and dramatic neotectonic movement in the distribution range of this species could result in the high genetic differentiation. 2. Phylogeographic analysis based on nuclear ribosomal sequences, We sequenced the nrDNA ITS in all 27 populations sampled, 7 haplotypes were identified, among which C. micholitzii had 6, while C. multipinnata, C. longipetiolula and C. debaoensis shared the remaining one. Compared to chloroplast genes, nuclear genes had higher correlation between genetic and geographical distance, but lower interspecies differentiation (54.42% vs 25.24%). Phylogeographical structure of C. micholitzii and C.bifida based on ITS Variation was consistent with the morphology differentiation. This similar in nuclear gene should be ascribed to pollen-mediated gene flow among geographically proximate populations.Long-distance gene flow over the two groups was clearly interrupted, which brought on the nrDNA genetic differenciation between the geographically isolated groups, to a certain extent affected the morphological variation. 3. Interspecies relationships among Cycas micholitzii complex, We analysed chloroplast sequence variation of the atpB-rbcL and psbA-trnH intergenic spacers in 27 populations sampled of C. micholitzii complex, AMOVA analysis showed that the component of among-species/region component (59.21%). However, phylogenic analysis showed that the haplotypes of C. micholitzii complex couldn`t grouped into four clusters closely corresponding to the narrowly defined C. micholitzi, C. multipinnata, C. debaoensis and C. longipetiolula. We concluded that the conflict may result from several factors: firstly incomplete lineage sorting of C. micholitzii; secondly hybridization/introgression of sympatrically cycads, which would be supported by evidence base on nrDNA ITS sequences; thirdly intramolecular recombination in cpDNA of cycads; eventually the neotectonic movement in the distribution range of this species.","jscount":"1","jsurl":"/simple-search?field1=all&rpp=10&accurate=false&advanced=false&sort_by=2&isNonaffiliated=false&search_type=-1&query1=Arctic-alpine%2BTaxa&order=desc&&fq=dc.project.title_filter%3ACycas%5C+micholitzii%5C+complex%5C+is%5C+composed%5C+of%5C+5%5C+species%5C%3A%5C+C.%5C+micholitzii%5C+Dyer%2C%5C+C.%5C+bifida%5C+%5C%28Dyer%5C%29%5C+K.%5C+D.%5C+Hill%2CC.%5C+longipetiolula%5C+D.%5C+Y.%5C+Wang%2C%5C+C.%5C+debaoensis%5C+Y.%5C+C.%5C+Zhong%5C+et%5C+C%5C+J.%5C+Chen%2C%5C+C.%5C+multipinnata%5C+C%5C+J.%5C+Chen%5C+et%5C+S.%5C+Y.%5C+Yang%EF%BC%8Cand%5C+distributed%5C+from%5C+southwest%5C+China%5C+to%5C+central%5C+Vietnam%5C+and%5C+eastern%5C+Laos.%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+nuclear%5C+DNA%5C+fragments%2C%5C+our%5C+study%5C+revealed%5C+the%5C+population%5C+genetic%5C+structure%5C+of%5C+C.%5C+micholitzii%5C+complex%5C+and%5C+explored%5C+the%5C+potential%5C+causes.%5C+The%5C+evolutionary%5C+and%5C+demographic%5C+histories%5C+were%5C+investigated.%5C+The%5C+genetic%5C+relationship%5C+among%5C+species%5C+in%5C+the%5C+complex%5C+was%5C+also%5C+clarified.The%5C+results%5C+were%5C+summarized%5C+as%5C+follows%5C%3A%5C+1.%5C+Phylogeographic%5C+analysis%5C+based%5C+on%5C+chloroplast%5C+sequences%EF%BC%8CWe%5C+examined%5C+chloroplast%5C+sequence%5C+variation%5C+of%5C+the%5C+atpB%5C-rbcLand%5C+psbA%5C-trnHintergenic%5C+spacers%5C+in%5C+27%5C+populations%5C+of%5C+C.%5C+micholitzii%5C+complex%2C%5C+recovering%5C+26%5C+haplotypes.%5C+The%5C+average%5C+within%5C-population%5C+diversity%5C+%5C%28HS%5C+%3D%5C+0.140%5C%29%5C+was%5C+low%5C+while%5C+total%5C+diversity%5C+%5C%28HT%5C+%3D%5C+0.911%5C%29%5C+was%5C+high.%5C+Population%5C+differentiation%5C+was%5C+also%5C+high%5C%28GST%5C+%3D%5C+0.846%2C%5C+NST%5C+%3D%5C+0.919%5C%29%2C%5C+indicating%5C+significant%5C+phylogeographical%5C+structure%5C+%5C%28NST%5C+%3E%5C+GST%2Cp%5C+%3C%5C+0.001%5C%29%5C+and%5C+low%5C+levels%5C+of%5C+seed%5C-based%5C+gene%5C+flow.%5C+C.%5C+debaoensis%5C+%5C%28Cycadaceae%5C%29%5C+is%5C+an%5C+endangered%5C+species%5C+restricted%5C+to%5C+the%5C+border%5C+of%5C+Guangxi%5C+and%5C+Yunnan%5C+province%5C+in%5C+southwest%5C+China.%5C+This%5C+species%5C+has%5C+been%5C+classified%5C+into%5C+two%5C+types%5C%3A%5C+sand%5C+and%5C+karst%2C%5C+according%5C+to%5C+the%5C+soil%5C+matrix%5C+they%5C+grow%5C+on.%5C+We%5C+examined%5C+chloroplast%5C+sequence%5C+variation%5C+of%5C+the%5C+cpDNA%5C+sequences%5C+from%5C+11%5C+populations%5C+of%5C+this%5C+species.%5C+Significant%5C+population%5C+genetic%5C+differentiation%5C+was%5C+detected%5C+%5C%28GST%3D%5C+0.684%5C+and%5C+FST%5C+%3D%5C+0.74160%5C%29.%5C+There%5C+was%5C+marked%5C+genetic%5C+differentiation%5C+between%5C+populations%5C+in%5C+the%5C+sand%5C+and%5C+karst%5C+regions%5C+and%5C+no%5C+expansion%5C+was%5C+detected.%5C+Climate%5C+changes%5C+during%5C+glacial%5C+periods%5C+have%5C+had%5C+significant%5C+effects%5C+on%5C+the%5C+current%5C+distribution%5C+of%5C+cycads.%5C+The%5C+molecular%5C+phylogenetic%5C+data%2C%5C+together%5C+with%5C+the%5C+geographic%5C+distribution%5C+of%5C+the%5C+haplotypes%2C%5C+suggest%5C+that%5C+C.%5C+debaoensis%5C+experienced%5C+range%5C+contraction%5C+during%5C+glacial%5C+periods%2C%5C+and%5C+that%5C+the%5C+current%5C+populations%5C+are%5C+still%5C+confined%5C+to%5C+the%5C+original%5C+refugia%5C+in%5C+southwest%5C+China%5C+which%5C+have%5C+favorable%5C+habitats%5C+in%5C+glacial%5C+period.%5C+These%5C+results%5C+imply%5C+that%5C+small%5C+refugia%5C+were%5C+maintained%5C+in%5C+both%5C+sand%5C+and%5C+karst%5C+regions%5C+during%5C+the%5C+LGM%5C+%5C%28last%5C+glacial%5C+maximum%5C%29.%5C+This%5C+species%5C+had%5C+no%5C+postglacial%5C+recolonization%5C+and%5C+only%5C+stayed%5C+in%5C+these%5C+refugia%5C+up%5C+to%5C+now.%5C+The%5C+low%5C+within%5C-population%5C+diversity%5C+of%5C+C.%5C+debaoensis%5C+suggests%5C+that%5C+there%5C+were%5C+strong%5C+bottleneck%5C+events%5C+or%5C+founder%5C+effects%5C+within%5C+each%5C+separate%5C+region%5C+during%5C+the%5C+Quaternary%5C+climatic%5C+oscillations.%5C+Relatively%5C+high%5C+genetic%5C+and%5C+haplotype%5C+diversities%5C+were%5C+detected%5C+in%5C+the%5C+newly%5C+discovered%5C+populations%2C%5C+which%5C+located%5C+at%5C+intermediate%5C+locality%5C+of%5C+sand%5C+regions%5C+and%5C+had%5C+morphological%5C+variation%5C%3B%5C+this%5C+is%5C+probably%5C+the%5C+consequence%5C+of%5C+the%5C+admixture%5C+of%5C+different%5C+haplotypes%5C+colonizing%5C+the%5C+area%5C+from%5C+separate%5C+sources.%5C+%5C+C.%5C+micholitzii%5C+occurs%5C+in%5C+the%5C+Annan%5C+Highlands%5C+in%5C+central%5C+Vietnam%5C+near%5C+the%5C+Laos%5C+border.%5C+C.%5C+bifida%5C+occurs%5C+in%5C+North%5C+Vietnam%5C%3B%5C+its%5C+distribution%5C+extends%5C+across%5C+the%5C+border%5C+into%5C+adjacent%5C+localities%5C+in%5C+Guangxi%5C+and%5C+Yunnan%5C+in%5C+China.%5C+For%5C+the%5C+comparability%5C+between%5C+them%2Ctheywere%5C+considered%5C+as%5C+the%5C+same%5C+species%5C+C.%5C+micholitzii%5C+by%5C+many%5C+acade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a field trip at a brule in Shangri-La, a mixed population of Ligularia Cass. was found, which including L. subspicata (Bur. et Franch.) Hand.-Mazz., L. nelumbifolia (Bur. et Franch.) Hand.-Mazz., L. tongolensis (Franch.) Hand.-Mazz., L. cymbulifera (W.W.Smith) Hand.-Mazz., L. lingiana S.W.Liu, and also some individuals morphologically intermediate between L. subspicata and L. nelumbifolia. Hence, these intermediate individuals were preliminarily assumed as natural hybrids of the two Ligularia. According to their morphology, they’re assumed to form hybrids A and B. Through careful comparison of specimens in herbarium and those we collected, the inflorescence of putative hybrid A is close to L. nelumbifolia, but the shape of laminae are intergradation of L. subspicata and L. nelumbifolia; overall morphology of putative hybrids B is similar to L. nelumbifolia, but inflorescence color is as same as L. subspicata. Compared to L. nelumbifolia (39%) and L. subspicata (36.8%), the germination rate of putative hybrid B (45.7%) slightly higher than the two; but that of hybrid A is extraordinarily low (0.3%). One possible interpretation of the low rate is hybridization. 60 individuals were collected, including putative parents, other 4 species of Ligularia nearby, putative hybrid A and B. They were all direct sequenced of four cpDNA fragments, and direct sequenced or cloning sequenced of nrDNA ITS4-5. The results support that L. nelumbifolia and L. subspicata are parents of putative hybrid A, and the majority female parent is L. subspicata, L. vellerea may also be involved in the hybridization in some degree; the nuclear sequences of putative hybrid B have no superposition, and its chloroplast DNA sequences are identical with L. nelumbifolia, so putative hybrid B could not be hybrid; and there are backcross individuals exist among the putative parent L. subspicata. NewHybrids analysis of ISSR markers indicated that, the individuals of putative hybrid A are almost L. nelumbifolia and L. subspicata F1 hybrid generation (10/11), only 1/11 possibly backcross or other forms; all individuals of hybrid B are L. nelumbifolia; except one individual of L. subspicata as backcrossed, the other parent individuals are 100% reliable. This study focused on molecular evidence, complemented by ecological, reproductive and other characteristics, we demonstrated that the morphologically intermediate individuals’ origin, and the probability of belonging to each parental or hybrid class. And concluded that L. nelumbifolia and L. subspicata are the parents of putative hybrid A, L. vellerea may also be involved in the hybridization in some degree, hybrids mainly are the first generation, a few individuals may be involved in backcross, and most probably backcross with L. subspicata according to the anthesis, while the assumption of hybrid B is not 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MSCA individual fellowship[705432]","jscount":"1","jsurl":"/simple-search?field1=all&rpp=10&accurate=false&advanced=false&sort_by=2&isNonaffiliated=false&search_type=-1&query1=Arctic-alpine%2BTaxa&order=desc&&fq=dc.project.title_filter%3AEU%5C+MSCA%5C+individual%5C+fellowship%5C%5B705432%5C%5D"},{"jsname":"EU MSCA individual fellowship[750252]","jscount":"1","jsurl":"/simple-search?field1=all&rpp=10&accurate=false&advanced=false&sort_by=2&isNonaffiliated=false&search_type=-1&query1=Arctic-alpine%2BTaxa&order=desc&&fq=dc.project.title_filter%3AEU%5C+MSCA%5C+individual%5C+fellowship%5C%5B750252%5C%5D"},{"jsname":"European Research Council through the Advanced Grant Project TREEPEACE[FP7-339728]","jscount":"1","jsurl":"/simple-search?field1=all&rpp=10&accurate=false&advanced=false&sort_by=2&isNonaffiliated=false&search_type=-1&query1=Arctic-alpine%2BTaxa&order=desc&&fq=dc.project.title_filter%3AEuropean%5C+Research%5C+Council%5C+through%5C+the%5C+Advanced%5C+Grant%5C+Project%5C+TREEPEACE%5C%5BFP7%5C-339728%5C%5D"},{"jsname":"Following the rapid uplift of the Himalaya, the reorganization of the major river drainages was primarily caused by river capture events，e.g. those of the Jinshajiang River (comprising the Upper, Middle and Lower Jinshajiang) and its tributaries (Yalongjiang, Daduhe, Jialingjiang), the Nujiang, the Lancangjiang, and the Honghe. We selected Terminalia franchetii var. franchetii and T. franchetii var. intricata in the Sino-Himalayan region to study the relationship with Honghe diversion events. The distribution of this species is predicted to have retained genetic signatures of past hydrological landscape structures. The major result as flowing:1. Chloroplast phylogeography of T. franchetii based on haplotype analysis，Based on a range-wide sampling comprising 28 populations and 258 individuals, and using chloroplast DNA sequences (trnL-trnF, petL-psbE), we detected 12 haplotypes. Terminalia franchetii was found to harbour high haplotype diversity (hT = 0.784) but low average within-population diversity (hS = 0.124). The analysis of genetic structure using SAMOVA showed that the number of population groups equaled five, and all the haplotypes can be divided into five groups. Group B and C identified exhibited a disjunctive distribution of dominant haplotypes between northern and southern valleys, corresponding to the geography of past rather than modern drainage systems.Mismatch distribution (multimodal curve) and neutral tests provided no evidence of recent demographic population growth. We suggest that the modern disjunctive distribution of T. franchetii, and associated patterns of cpDNA haplotype variation, result from vicariance caused by several historical river separation and capture events. By assuming a common mutation rate of the cpDNA-IGS regions, our inferred timings of these events (0.82-4.39 Mya) broadly agrees with both previous geological and molecular estimated time of drainage rearrangements in this region. So we conclude that there were several historical vicariance events play a major role for the distribution of T. franchetii in this region.2. Genetic diversity and structure of T. franchetii var. franchetii based on AFLP analysis，We determined the genotype of 251 individuals of T. franchetii var. franchetii from 21 populations using amplified fragment length polymorphism (AFLP), for our aim is only investigated the relationship between the modern distribution of T. franchetii and geological changes in drainage patterns. The overall estimate of genetic structure (Gst) was 0.249, indicating that clear genetic differentiation existed among the populations. Estimates of gene flow (Nm = 0.754) between populations based on the Gst value revealed that the number of migrants per generation is not frequently.Using Neighbor-Joining tree, Principal Coordinates Analysis, STRUCTURE and network methods, Analyses of AFLP markers identified two main population groups (I and II) and four subgroups (A – D) of T. franchetii. Genetic diversity was lower in Group I than in Group II. The results show that Groups I and II probably once occupied continuous areas respectively along ancient drainage systems and there were several historical separation and capture events that can account for the distribution of T. franchetii in this region. After all，these are good examples of the way in which historical events can change a species’ distribution from continuous to fragmented (Jinshajiang/ Yalongjiang and Honghe), and a disjunct distribution to a continuous one (Upper/Lower Jinshajiang and Yalongjiang). The results provide new insights into the phylogeographic pattern of plants in southwest China.3. Relationships between T. franchetii var. franchetii and T. franchetii var. intricata ，While T. franchetii var. Franchetii and var. intricata slightly differ in overall size and leaf hairiness, these taxa did not exhibit reciprocal monophyly. As results show, the genetic difference between the two varieties is much smaller than that within var. franchetii (Salween population vs. other populationsof this variety). It is also revealed in a phylogenetic analysis of ITS region of Combretoideae. The habitats of var. franchetii and var. intricata have obviously difference. Thus, the differences between the two varieties in overall size and leaf hairiness might reflect different phenotypic responses to environmental changes and the divergent environmental niche spaces they occupy. Based on the reasoning above, we agree with Flora of China that “T. intricata” represents a variety of T. franchetii rather than a separate 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Natural Science Foundation of China[41671280]","jscount":"1","jsurl":"/simple-search?field1=all&rpp=10&accurate=false&advanced=false&sort_by=2&isNonaffiliated=false&search_type=-1&query1=Arctic-alpine%2BTaxa&order=desc&&fq=dc.project.title_filter%3ANational%5C+Natural%5C+Science%5C+Foundation%5C+of%5C+China%5C%5B41671280%5C%5D"},{"jsname":"National Natural Science Foundation of China[41701317]","jscount":"1","jsurl":"/simple-search?field1=all&rpp=10&accurate=false&advanced=false&sort_by=2&isNonaffiliated=false&search_type=-1&query1=Arctic-alpine%2BTaxa&order=desc&&fq=dc.project.title_filter%3ANational%5C+Natural%5C+Science%5C+Foundation%5C+of%5C+China%5C%5B41701317%5C%5D"},{"jsname":"Northwestern Yunnan is one of the differentiation center of modern Rhododendron L.. Rhododendron species are the major composition of alpine and sub-alpine vegetation and the play vital roles in ecosystem in this region. Ericoid Mycorrhizas (ERM) is a specific mycorrhizal type between fungi and plants of three families in the Ericales: Ericaceae, Empetraceae and Epacridaceae. ERM play important roles in mediating stress and enhancing endurance of plants to survive in harsh wild condition. In order to find out the species diversity and function of ERM fungi in Rhododendron species in Yunnan, China, the multidisciplinary preliminary studies were performed: 1) The living environment of natural populations was investigated, and then roots of Rhododendron in natural populations were observed. 2) Three species of R. decorum, R. pachypodum and R. phaeochrysum were chosen to isolate and culture fungi from their toots. 3) Among them, species diversity and distribution of ERM fungi in R. decorum from three populations were identified and compared by morphological characteristics, molecular method and Simpson index. 4) The preliminary effect of ERM fungi on sterile seedlings of R. decorum was evaluated. The main results are summarized as follows.1. Living environment of Rhododendron,The result of field investigation showed that elevation altitude of Rhododendron distribution ranges from 2500m to 4650m. Some species such as R. telmateium and R. phaeochrysum grow in limestone and mine tailing areas with the pH of soil 7.0-7.1. Most plants grow in alpine coniferous, evergreen and deciduous broad-leaved mixed-wide forest, and the pH of soil is 5.4-6.9.2. Roots section observation, Roots section observation showed that ERM hyphal coils were present in epidermal cells of all hair roots of 17 Rhododendron species. In addition, we found clamp connections in the roots of 8 species in 19 populations. Dark septate endophytes were recognized in the hair roots under light microscope, too. It showed that ascomycetes and basidiomycetes might coexist in the roots. 3. Morphological characteristics of colonies,Nearly 400 slow-growing colonies were isolated and cultured in PDA medium from 500 roots of R. decorum, R. pachypodum and R. phaeochrysum. Their morphological characteristics were various. For example, the texture included fluffy, felty, floccose, and so on. The ridge shape is radialized, round or irregular. Some culture exudated white, brown or dark liquids during growth period. The shape of their conidiospore is round, spindly, bacilliform, and so on. Their growth rate ranges from 0.2-4mm/d (the growth of diameter of culture every day), while some are determinate growth. There were some isolations occurred many times while others occurred only one time in the culture. There were many different colonies among different Rhododendron and different populations especcially R. phaeochrysum. 4. Species diversity of ERM fungi in R. decorum,Twenty hundred and eighteen slow-growing colonies were isolated from R. decorum and 125 of them were ericoid mycorrhizal fungi. By observing morphological characteristics and using sequences of the nuclear ribosomal DNA ITS region, we identified them as 12 species. Except for 3 unidentified isolates, the other 9 belonged to 9 genera, 4 orders of Pezizomycotina. Four isolate morphotypes belong to Helotiales, so they are the dominant ERM species. Oidodendron maius (FJ999645) holds 18.4% of the whole cultured ERM fungi of R. decorum. However, its distribution was different among three populations. The ERM fungi isolated from R. decorum are rich and they are different from other reports in other regions. Some species were not reported as ERM fungi in other reportes such as Neonectria radicicola, Bionectria ochroleuca, and so on. There were 11，8 and 8 ERM fungi respectively in three populations with 7 occurred in three populations. It shows that total species diversity of mycorrhizal fungi isolated from R. decorm was high, with Simpson index 0.86 and Shannon-Weiner index 3.02. The species diversity of wild populations was higher than cultivated one. 5. Preliminary effect of ERM fungi on sterile seedlings of R. decorum,Thirty-eight representative isolates were chosen to test their ability of forming ERM with sterile seedlings of R. decorum and 28 were successful. The mycorrhizal seedlings are much higher and stronger than ordinary sterile seedlings. Their roots are much longer and intensive, too. The root tips and other region of mycorrhizal seedlings are brown with many hyphae around the root surface or penetrate the epidermal cells to form hyphal coils. But the sterile roots are white without any hyphae or hyphal coils in the 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is one of the largest families in angiosperm, but sadly they are among the most threatened of plants due to over collection and habitat loss. The conservation of orchids is more important and imminent under current climatic change scenarios. Orchids always have complex ecological interactions with pollinators, therefore it is critical to know their pollination strategies when apply conservation policy and techniques. The slipper orchids of Cypripedium Section Trigonopedia were thought to be pollinated by flies, yet no detailed experimental evidence was provided until now. The genus Calanthe comprises 150 species, only three of them have been observed their pollinators. In this dissertation, we investigated the pollination ecology of three orchids, Cypripedium fargesii Franch., Calanthe yaoshanensis Z. X. Ren et H. Wang and C. tricarinata Lindl. at the Yaoshan National Natural Reserve, Qiaojia, northeastern Yunnan, China. This study examined habitat, phenology, floral traits, pollinators, floral scent and reproductive success for each orchid. We dissected their pollination systems and deciphered attraction mechanisms involved. Finally we provided a conservation strategy for each orchid. 1. Breeding system, Cypripedium fargesii, Calanthe yaoshanensis and C. tricarinata are all self-compatible. However, there are no autogamy mechanisms under natural conditions; pollinators are needed for successful reproduction. The proportion of fully developed and viable embryos of cross-pollinated seeds is significantly higher than self-pollinated seeds. Post-zygotic fatality was the main cause for aborted embryo development of self-pollinated ovaries. 2. Pollination ecology of Cypripdium fargesii, Cypripedium fargesii is almost exclusively pollinated by mycophilous flat-footed flies in the genus Agathomyia (Platypezidae, Diptera). Our study is the first to report the flat-footed fly to be the pollinator of flowering plants. We suggest a novel deceptive pollination system that specifically targets flat-footed flies in C. fargesii. The orchid accomplishes its deception through morphology and offactory mimicry of ascomycete fungi infected leaves：(1) We found mycelia and conidia of Cladosporium sp. (Davidiellaceae) on the surface of mouthparts and tarsi of examined flies, this indicates that adult Agathomyia fly is feeding on fungal spores. Cladosporium always infects leaves and fruits of wild and cultivate plants and causes black mold spots on the surface of leaves and fruits. (2) The upper surface of orchid leaves are scattered with black or blackish maroon spots, also with a cluster of multicells chain-like trichome at the center of spots. These spots are similar to fungi infected mold spots on the surface of leaves. (3) The flower produce more than 50 scent molecules associated with a wide variety of flowers, leaves and fruits. 3-methyl-1-butanol, 2-ethyl-1-hexanol and 1-Hexanol are also detected from Cladosporium, and 3-methyl-1-butanol is a typical microbial organic compound. The leaves of orchids and scent molecules mimic of ascomycete fungi infected leaves to attract flat-footed flies to find fungal spores for food. The orchid utilizes the special food habit and feeding behaviours of flat-footed flies. 3. Pollination ecology of Calanthe yaoshanensis. Calanthe yaoshanensis Z. X. Ren et H. Wang is a new species published by author. The main pollinator is drone fly (Eristalis tenax). C. yaoshanensis provides no reward to insect visitors, its pollination strategy is generalized food deception. The pollinators of C. yaoshanensis are attracted to bright yellow-colored perianths and alcohol-related sweet scent of the flowers. 4. Pollination ecology of Calanthe tricarinata, The insect visitation to C. tricarinata is very scarce, and Bombus patagiatus, the primary pollinator, carries pollinaria on its head. The pollination strategy is generalized food deception. The bumble bees are probably attracted by the yellow-colored sepals and petals, and brick-red lip of the orchid flowers. The fruit set is very low, 1.20%, 2.96% and 2.74% for 2008 to 2010 years, significant difference among three years. Low fruit set is due to severe pollinator limitation in over-grazing habitat. 5. Conservation strategies, Cypripedium fargesii is suggested to be conserved in situ, and both in situ and ex situ are recommended for conservation of two Calanthe 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and Cypripedium are close relatives belonging to the subfamily Cypripedioideae. However, they undergo considerable divergence in the aspects of life forms, leaf traits and habitats. In present study, leaf morphologies and anatomical structures, leaf lifespans, leaf mass per area, photosynthetic capacities, nutrient use efficiencies, leaf construction costs, and maintenance costs were investigated to understand the relationship between leaf traits and ecophysiological adaptability of the two types of plants and explore the related ecological and evolutionary significances. The results suggest that:1. Compared with Cypripedium, Paphiopedilum was characterized by drought tolerance from its leaf anatomical structure including fleshy leaf, thicker surface cuticle, huge abaxial epidermis cells, differentiation of palisade and spongy mesophyll layers, the prominent of mucilaginous substances, supportable leaf main vein, lower total stoma area (%), sunken stomata and special stoma structure. Leaf morphologies and structures of Cypripedium were to the contrary of Paphiopedilum. Leaf morphologies and structures embodied the adaptation to the environment in both Paphiopedilum and Cypripedium. Our results also confirmed the previous observation that Paphiopedilum was the only genus that did not possess guard cell chloroplasts.2. The photosynthetic capacities of P. armeniacum leaves were different with different leaf ages. The highest photosynthetic capacity occurred in leaf age 1-2 years, followed by 1 year and 2-4 years. The highest photosynthetic capacity of C. flavum occurred in leaf age 60 days, followed by 30 days, 90 days and 120 days. 3. Photosynthetic capacities of different leaf positions were mainly affected by leaf ages in P. armeniacum. The four leaves lying on the top did the most accumulation of the assimilation products in the whole plant. The leaves of sequence number > 6 could use lots of photosynthates, but contributed little to the accumulation of biomass. 4. Photosynthetic rate of P. armeniacum decreased a little at the noon, and the highest photosynthetic rate was observed at 10:00h in the greenhouse. The variation of photosynthetic rate was in the same trend as stomatal conductance. Higher relative humidity seemed to be the key for higher photosynthetic rate in P. armeniacum. 5. The photosynthetic capacity of C. flavum was statistically larger than that of P. armeniacum. The lower leaf photosynthetic capacity of P. armeniacum was related to its lower leaf nitrogen concentration,leaf phosphorus concentration and enzyme activities. Meanwhile, the extremely lower stomatal conductance and internal mesophyll conductance might greatly limit the photosynthetic capacity of P. armeniacum. The lower stomatal conductance and photosynthetic rate of Paphiopedilum might partially caused by the lack of chloroplasts in the guard cell of Paphiopedilum. Compared with C. flavum, P. armeniacum was more fond of shade environment.6. The short longevity leaf of Cypripedium had bigger photosynthetic capacity and greater potential for fast growth. But the longer LL of Paphiopedilum enhanced nutrient conservation which could compensate its lower photosynthetic capacity. The short longevity leaf of Cypripedium usually had higher photosynthetic rate per unit leaf mass and dark respiration rate, and photosynthetic capacity decreased fast with leaf age. However, for Paphiopedilum, the situation was the opposite. 7. Compared with Cypripedium, Paphiopedilum had higher water use efficiency and lower photosynthetic nitrogen use efficiency. 8. The leaf of Paphiopedilum had higher leaf construction cost and longer repayment time than that of Cypripedium. The leaf structures and physiological functions of Paphiopedilum and Cypripedium reflected the adaptation to their habitats. The leaf morphological and physiological evolution of Paphiopedilum was related to water and resource-conserving traits in the karst habitat. The leaf traits of Cypripedium were the adaptation to the environment rich in water and nutrients but easy to change with seasons.Our results provided evidence of divergent evolution of congeneric orchids under natural selection.","jscount":"1","jsurl":"/simple-search?field1=all&rpp=10&accurate=false&advanced=false&sort_by=2&isNonaffiliated=false&search_type=-1&query1=Arctic-alpine%2BTaxa&order=desc&&fq=dc.project.title_filter%3APaphiopedilum%5C+and%5C+Cypripedium%5C+are%5C+close%5C+relatives%5C+belonging%5C+to%5C+the%5C+subfamily%5C+Cypripedioideae.%5C+However%2C%5C+they%5C+undergo%5C+considerable%5C+divergence%5C+in%5C+the%5C+aspects%5C+of%5C+life%5C+forms%2C%5C+leaf%5C+traits%5C+and%5C+habitats.%5C+In%5C+present%5C+study%2C%5C+leaf%5C+morphologies%5C+and%5C+anatomical%5C+structures%2C%5C+leaf%5C+lifespans%2C%5C+leaf%5C+mass%5C+per%5C+area%2C%5C+photosynthetic%5C+capacities%2C%5C+nutrient%5C+use%5C+efficiencies%2C%5C+leaf%5C+construction%5C+costs%2C%5C+and%5C+maintenance%5C+costs%5C+were%5C+investigated%5C+to%5C+understand%5C+the%5C+relationship%5C+between%5C+leaf%5C+traits%5C+and%5C+ecophysiological%5C+adaptability%5C+of%5C+the%5C+two%5C+types%5C+of%5C+plants%5C+and%5C+explore%5C+the%5C+related%5C+ecological%5C+and%5C+evolutionary%5C+significances.%5C+The%5C+results%5C+suggest%5C+that%5C%3A1.%5C+Compared%5C+with%5C+Cypripedium%2C%5C+Paphiopedilum%5C+was%5C+characterized%5C+by%5C+drought%5C+tolerance%5C+from%5C+its%5C+leaf%5C+anatomical%5C+structure%5C+including%5C+fleshy%5C+leaf%2C%5C+thicker%5C+surface%5C+cuticle%2C%5C+huge%5C+abaxial%5C+epidermis%5C+cells%2C%5C+differentiation%5C+of%5C+palisade%5C+and%5C+spongy%5C+mesophyll%5C+layers%2C%5C+the%5C+prominent%5C+of%5C+mucilaginous%5C+substances%2C%5C+supportable%5C+leaf%5C+main%5C+vein%2C%5C+lower%5C+total%5C+stoma%5C+area%5C+%5C%28%25%5C%29%2C%5C+sunken%5C+stomata%5C+and%5C+special%5C+stoma%5C+structure.%5C+Leaf%5C+morphologies%5C+and%5C+structures%5C+of%5C+Cypripedium%5C+were%5C+to%5C+the%5C+contrary%5C+of%5C+Paphiopedilum.%5C+Leaf%5C+morphologies%5C+and%5C+structures%5C+embodied%5C+the%5C+adaptation%5C+to%5C+the%5C+environment%5C+in%5C+both%5C+Paphiopedilum%5C+and%5C+Cypripedium.%5C+Our%5C+results%5C+also%5C+confirmed%5C+the%5C+previous%5C+observation%5C+that%5C+Paphiopedilum%5C+was%5C+the%5C+only%5C+genus%5C+that%5C+did%5C+not%5C+possess%5C+guard%5C+cell%5C+chloroplasts.2.%5C+The%5C+photosynthetic%5C+capacities%5C+of%5C+P.%5C+armeniacum%5C+leaves%5C+were%5C+different%5C+with%5C+different%5C+leaf%5C+ages.%5C+The%5C+highest%5C+photosynthetic%5C+capacity%5C+occurred%5C+in%5C+leaf%5C+age%5C+1%5C-2%5C+years%2C%5C+followed%5C+by%5C+1%5C+year%5C+and%5C+2%5C-4%5C+years.%5C+The%5C+highest%5C+photosynthetic%5C+capacity%5C+of%5C+C.%5C+flavum%5C+occurred%5C+in%5C+leaf%5C+age%5C+60%5C+days%2C%5C+followed%5C+by%5C+30%5C+days%2C%5C+90%5C+days%5C+and%5C+120%5C+days.%5C+3.%5C+Photosynthetic%5C+capacities%5C+of%5C+different%5C+leaf%5C+positions%5C+were%5C+mainly%5C+affected%5C+by%5C+leaf%5C+ages%5C+in%5C+P.%5C+armeniacum.%5C+The%5C+four%5C+leaves%5C+lying%5C+on%5C+the%5C+top%5C+did%5C+the%5C+most%5C+accumulation%5C+of%5C+the%5C+assimilation%5C+products%5C+in%5C+the%5C+whole%5C+plant.%5C+The%5C+leaves%5C+of%5C+sequence%5C+number%5C+%3E%5C+6%5C+could%5C+use%5C+lots%5C+of%5C+photosynthates%2C%5C+but%5C+contributed%5C+little%5C+to%5C+the%5C+accumulation%5C+of%5C+biomass.%5C+4.%5C+Photosynthetic%5C+rate%5C+of%5C+P.%5C+armeniacum%5C+decreased%5C+a%5C+little%5C+at%5C+the%5C+noon%2C%5C+and%5C+the%5C+highest%5C+photosynthetic%5C+rate%5C+was%5C+observed%5C+at%5C+10%5C%3A00h%5C+in%5C+the%5C+greenhouse.%5C+The%5C+variation%5C+of%5C+photosynthetic%5C+rate%5C+was%5C+in%5C+the%5C+same%5C+trend%5C+as%5C+stomatal%5C+conductance.%5C+Higher%5C+relative%5C+humidity%5C+seemed%5C+to%5C+be%5C+the%5C+key%5C+for%5C+higher%5C+photosynthetic%5C+rate%5C+in%5C+P.%5C+armeniacum.%5C+5.%5C+The%5C+photosynthetic%5C+capacity%5C+of%5C+C.%5C+flavum%5C+was%5C+statistically%5C+larger%5C+than%5C+that%5C+of%5C+P.%5C+armeniacum.%5C+The%5C+lower%5C+leaf%5C+photosynthetic%5C+capacity%5C+of%5C+P.%5C+armeniacum%5C+was%5C+related%5C+to%5C+its%5C+lower%5C+leaf%5C+nitrogen%5C+concentration%2Cleaf%5C+phosphorus%5C+concentration%5C+and%5C+enzyme%5C+activities.%5C+Meanwhile%2C%5C+the%5C+extremely%5C+lower%5C+stomatal%5C+conductance%5C+and%5C+internal%5C+mesophyll%5C+conductance%5C+might%5C+greatly%5C+limit%5C+the%5C+photosynthetic%5C+capacity%5C+of%5C+P.%5C+armeniacum.%5C+The%5C+lower%5C+stomatal%5C+conductance%5C+and%5C+photosynthetic%5C+rate%5C+of%5C+Paphiopedilum%5C+might%5C+partially%5C+caused%5C+by%5C+the%5C+lack%5C+of%5C+chloroplasts%5C+in%5C+the%5C+guard%5C+cell%5C+of%5C+Paphiopedilum.%5C+Compared%5C+with%5C+C.%5C+flavum%2C%5C+P.%5C+armeniacum%5C+was%5C+more%5C+fond%5C+of%5C+shade%5C+environment.6.%5C+The%5C+short%5C+longevity%5C+leaf%5C+of%5C+Cypripedium%5C+had%5C+bigger%5C+photosynthetic%5C+capacity%5C+and%5C+greater%5C+potential%5C+for%5C+fast%5C+growth.%5C+But%5C+the%5C+longer%5C+LL%5C+of%5C+Paphiopedilum%5C+enhanced%5C+nutrient%5C+conservation%5C+which%5C+could%5C+compensate%5C+its%5C+lower%5C+photosynthetic%5C+capacity.%5C+The%5C+short%5C+longevity%5C+leaf%5C+of%5C+Cypripedium%5C+usually%5C+had%5C+higher%5C+photosynthetic%5C+rate%5C+per%5C+unit%5C+leaf%5C+mass%5C+and%5C+dark%5C+respiration%5C+rate%2C%5C+and%5C+photosynthetic%5C+capacity%5C+decreased%5C+fast%5C+with%5C+leaf%5C+age.%5C+However%2C%5C+for%5C+Paphiopedilum%2C%5C+the%5C+situation%5C+was%5C+the%5C+opposite.%5C+7.%5C+Compared%5C+with%5C+Cypripedium%2C%5C+Paphiopedilum%5C+had%5C+higher%5C+water%5C+use%5C+efficiency%5C+and%5C+lower%5C+photosynthetic%5C+nitrogen%5C+use%5C+efficiency.%5C+8.%5C+The%5C+leaf%5C+of%5C+Paphiopedilum%5C+had%5C+higher%5C+leaf%5C+construction%5C+cost%5C+and%5C+longer%5C+repayment%5C+time%5C+than%5C+that%5C+of%5C+Cypripedium.%5C+The%5C+leaf%5C+structures%5C+and%5C+physiological%5C+functions%5C+of%5C+Paphiopedilum%5C+and%5C+Cypripedium%5C+reflected%5C+the%5C+adaptation%5C+to%5C+their%5C+habitats.%5C+The%5C+leaf%5C+morphological%5C+and%5C+physiological%5C+evolution%5C+of%5C+Paphiopedilum%5C+was%5C+related%5C+to%5C+water%5C+and%5C+resource%5C-conserving%5C+traits%5C+in%5C+the%5C+karst%5C+habitat.%5C+The%5C+leaf%5C+traits%5C+of%5C+Cypripedium%5C+were%5C+the%5C+adaptation%5C+to%5C+the%5C+environment%5C+rich%5C+in%5C+water%5C+and%5C+nutrients%5C+but%5C+easy%5C+to%5C+change%5C+with%5C+seasons.Our%5C+results%5C+provided%5C+evidence%5C+of%5C+divergent%5C+evolution%5C+of%5C+congeneric%5C+orchids%5C+under%5C+natural%5C+selection."},{"jsname":"Plants respond to unpredictable alpine environments by a high degree of specialization in the structural and functional aspects of their flowers and pollination. However, few original data about the reproductive biology of these plants has been documented, particularly in the species-rich Himalaya-Hengduan Mountain regions. Incarvillea Juss. is notable for being a temperate and herbaceous member in the primarily tropical and woody family Bignoniaceae. Most species of the genus occur in alpine areas of the Himalaya-Hengduan Mountain regions. We investigated the reproductive biology of two alpine species, I. mairei and I. lutea. Incarvillea mairei was highly self-compatible, but depended on pollinators for seed production. The main pollinators were Halictus sp and Apis sp. at low altitude, and bumblebee at high altitude. Seed production was severely limited by pollinators, as indicated by supplemental hand-pollination experiments. The extended floral longevity and stigma receptivity greatly compensated for pollinator limitation. Outcrossing rates were high from 0.834 to 0.988 with altitude and cumulative inbreeding depression was 0.088, indicating a predominant outcrossing mating system. The combination of floral traits (approach herkogamy, sensitive stigma, anther appendages) and pollinator activities ensure a remarkably efficient pollination mechanism, as well as make it possible to ensure reproduction success in alpine habitats. Incarvillea lutea is self-compatible, but depends on insects for seed production. Both the fruit and seed set were high under natural conditions. The main pollinator is Halictus sp. The larger floral displays of I. lutea received more visitations, but facilitated geitonogamous pollination simultaneously. The cumulative inbreeding depression was 0.373. The corolla tube changed color with age from yellow to red. Young yellow flowers had a significant greater pollen and nectar reward. The co-occurrence of the change in amount of reward and flower color enabled I. lutea to direct pollinators to visit reproductive, highly rewarding yellow flowers. We suggest floral color change in I. lutea may serve as a mechanism for reducing geitonogamous pollination and increasing the efficiency of pollen transfer to enhance plant fitness.","jscount":"1","jsurl":"/simple-search?field1=all&rpp=10&accurate=false&advanced=false&sort_by=2&isNonaffiliated=false&search_type=-1&query1=Arctic-alpine%2BTaxa&order=desc&&fq=dc.project.title_filter%3APlants%5C+respond%5C+to%5C+unpredictable%5C+alpine%5C+environments%5C+by%5C+a%5C+high%5C+degree%5C+of%5C+specialization%5C+in%5C+the%5C+structural%5C+and%5C+functional%5C+aspects%5C+of%5C+their%5C+flowers%5C+and%5C+pollination.%5C+However%2C%5C+few%5C+original%5C+data%5C+about%5C+the%5C+reproductive%5C+biology%5C+of%5C+these%5C+plants%5C+has%5C+been%5C+documented%2C%5C+particularly%5C+in%5C+the%5C+species%5C-rich%5C+Himalaya%5C-Hengduan%5C+Mountain%5C+regions.%5C+Incarvillea%5C+Juss.%5C+is%5C+notable%5C+for%5C+being%5C+a%5C+temperate%5C+and%5C+herbaceous%5C+member%5C+in%5C+the%5C+primarily%5C+tropical%5C+and%5C+woody%5C+family%5C+Bignoniaceae.%5C+Most%5C+species%5C+of%5C+the%5C+genus%5C+occur%5C+in%5C+alpine%5C+areas%5C+of%5C+the%5C+Himalaya%5C-Hengduan%5C+Mountain%5C+regions.%5C+We%5C+investigated%5C+the%5C+reproductive%5C+biology%5C+of%5C+two%5C+alpine%5C+species%2C%5C+I.%5C+mairei%5C+and%5C+I.%5C+lutea.%5C+Incarvillea%5C+mairei%5C+was%5C+highly%5C+self%5C-compatible%2C%5C+but%5C+depended%5C+on%5C+pollinators%5C+for%5C+seed%5C+production.%5C+The%5C+main%5C+pollinators%5C+were%5C+Halictus%5C+sp%5C+and%5C+Apis%5C+sp.%5C+at%5C+low%5C+altitude%2C%5C+and%5C+bumblebee%5C+at%5C+high%5C+altitude.%5C+Seed%5C+production%5C+was%5C+severely%5C+limited%5C+by%5C+pollinators%2C%5C+as%5C+indicated%5C+by%5C+supplemental%5C+hand%5C-pollination%5C+experiments.%5C+The%5C+extended%5C+floral%5C+longevity%5C+and%5C+stigma%5C+receptivity%5C+greatly%5C+compensated%5C+for%5C+pollinator%5C+limitation.%5C+Outcrossing%5C+rates%5C+were%5C+high%5C+from%5C+0.834%5C+to%5C+0.988%5C+with%5C+altitude%5C+and%5C+cumulative%5C+inbreeding%5C+depression%5C+was%5C+0.088%2C%5C+indicating%5C+a%5C+predominant%5C+outcrossing%5C+mating%5C+system.%5C+The%5C+combination%5C+of%5C+floral%5C+traits%5C+%5C%28approach%5C+herkogamy%2C%5C+sensitive%5C+stigma%2C%5C+anther%5C+appendages%5C%29%5C+and%5C+pollinator%5C+activities%5C+ensure%5C+a%5C+remarkably%5C+efficient%5C+pollination%5C+mechanism%2C%5C+as%5C+well%5C+as%5C+make%5C+it%5C+possible%5C+to%5C+ensure%5C+reproduction%5C+success%5C+in%5C+alpine%5C+habitats.%5C+Incarvillea%5C+lutea%5C+is%5C+self%5C-compatible%2C%5C+but%5C+depends%5C+on%5C+insects%5C+for%5C+seed%5C+production.%5C+Both%5C+the%5C+fruit%5C+and%5C+seed%5C+set%5C+were%5C+high%5C+under%5C+natural%5C+conditions.%5C+The%5C+main%5C+pollinator%5C+is%5C+Halictus%5C+sp.%5C+The%5C+larger%5C+floral%5C+displays%5C+of%5C+I.%5C+lutea%5C+received%5C+more%5C+visitations%2C%5C+but%5C+facilitated%5C+geitonogamous%5C+pollination%5C+simultaneously.%5C+The%5C+cumulative%5C+inbreeding%5C+depression%5C+was%5C+0.373.%5C+The%5C+corolla%5C+tube%5C+changed%5C+color%5C+with%5C+age%5C+from%5C+yellow%5C+to%5C+red.%5C+Young%5C+yellow%5C+flowers%5C+had%5C+a%5C+significant%5C+greater%5C+pollen%5C+and%5C+nectar%5C+reward.%5C+The%5C+co%5C-occurrence%5C+of%5C+the%5C+change%5C+in%5C+amount%5C+of%5C+reward%5C+and%5C+flower%5C+color%5C+enabled%5C+I.%5C+lutea%5C+to%5C+direct%5C+pollinators%5C+to%5C+visit%5C+reproductive%2C%5C+highly%5C+rewarding%5C+yellow%5C+flowers.%5C+We%5C+suggest%5C+floral%5C+color%5C+change%5C+in%5C+I.%5C+lutea%5C+may%5C+serve%5C+as%5C+a%5C+mechanism%5C+for%5C+reducing%5C+geitonogamous%5C+pollination%5C+and%5C+increasing%5C+the%5C+efficiency%5C+of%5C+pollen%5C+transfer%5C+to%5C+enhance%5C+plant%5C+fitness."},{"jsname":"lastIndexed","jscount":"2024-05-24"}],"资助项目","dc.project.title_filter")'>
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Reproductive Allocation in Plants
期刊论文
Reproductive Allocation in Plants, 3111, 页码: 1—30
作者:
Shuhei Tanaka
;
Shin-ichiro Kochi
;
Heigo Kunita
;
Shin-ichi Ito
;
Mitsuro Kameya-Iwaki
Adobe PDF(180Kb)
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浏览/下载：148/1
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提交时间：2017/07/19
A global phylogeny of Lycopodiaceae (Lycopodiales; lycophytes) with the description of a new genus, Brownseya, from Oceania
期刊论文
TAXON, 2022, 卷号: 71, 期号: 1, 页码: 25-51
作者:
Chen,De-Kui
;
Zhou,Xin-Mao
;
Rothfels,Carl J.
;
Shepherd,Lara D.
;
Knapp,Ralf
;
Zhang,Liang
;
Lu,Ngan Thi
;
Fan,Xue-Ping
;
Wan,Xia
;
Gao,Xin-Fen
;
He,Hai
;
Zhang,Li-Bing
Adobe PDF(8520Kb)
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浏览/下载：156/8
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提交时间：2022/04/02
Huperzia
Lycophyte Phylogeny
Lycopodiella Serpentina
Phlegmariurus
Phylloglossum
Vascular Plant Evolution
Complete Chloroplast Genome
Lycopodiopsida Lycopodiaceae
Generic Classification
Spore Morphology
Early Evolution
Land Plants
Rbcl Gene
Huperzia
Sequence
Likelihood
Spatiotemporal maintenance of flora in the Himalaya biodiversity hotspot: Current knowledge and future perspectives
期刊论文
ECOLOGY AND EVOLUTION, 2021, 卷号: 11, 期号: 16, 页码: 10794-10812
作者:
Wambulwa,Moses C.
;
Milne,Richard
;
Wu,Zeng-Yuan
;
Spicer,Robert A.
;
Provan,Jim
;
Luo,Ya-Huang
;
Zhu,Guang-Fu
;
Wang,Wan-Ting
;
Wang,Hong
;
Gao,Lian-Ming
;
Li,De-Zhu
;
Liu,Jie
Adobe PDF(2089Kb)
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浏览/下载：173/61
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提交时间：2022/04/02
biodiversity hotspot
climate change
elevational gradient
Himalayan flora
mountain ecosystem
spatiotemporal diversification
SPECIES RICHNESS PATTERNS
QINGHAI-TIBET PLATEAU
SOUTH ASIAN MONSOON
ELEVATIONAL GRADIENT
HENGDUAN MOUNTAINS
CLIMATE-CHANGE
BETA-DIVERSITY
QUATERNARY GLACIATION
GENETIC CONSEQUENCES
ARTIFICIAL DISPERSAL
Diversity of Flower Visiting Beetles at Higher Elevations on the Yulong Snow Mountain (Yunnan, China)
期刊论文
DIVERSITY-BASEL, 2021, 卷号: 13, 期号: 11, 页码: 604
作者:
Li,Kai-Qin
;
Ren,Zong-Xin
;
Li,Qiang
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提交时间：2022/04/02
alpine
diversity
Hengduan Mountain
modularity
plant-insect interaction
FLORAL BIOLOGY
RAIN-FOREST
POLLINATION
COLEOPTERA
COMMUNITY
SPECIALIZATION
NETWORKS
SARAWAK
ANDES
Obtusifoliaceae, a new family of leafy liverworts to accommodate Konstantinovia, newly described from the Hengduan Mts. (South China) and Obtusifolium (Cephaloziineae, Marchantiophyta)
期刊论文
PLANT SYSTEMATICS AND EVOLUTION, 2021, 卷号: 307, 期号: 6, 页码: 62
作者:
Bakalin,Vadim A.
;
Fedosov,Vladimir E.
;
Fedorova,Alina V.
;
Ma,Wen Zhang
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浏览/下载：110/8
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提交时间：2022/04/02
Anastrophyllaceae
Biodiversity
Liverworts
Lophoziaceae
Paraphyly
Taxonomy
PHYLOGENETIC INFERENCE
TAXONOMIC REVISION
GENUS
SCAPANIACEAE
EVOLUTION
HEPATICAE
BRYOPHYTES
DIVERSITY
INSIGHTS
NORTH
Hidden in plain view: an example from Ptilidium (Ptilidiaceae, Marchantiophyta)
期刊论文
PHYTOTAXA, 2021, 卷号: 510, 期号: 1, 页码: 29-42
作者:
Bakalin,Vadim
;
Vilnet,Anna
;
Klimova,Ksenia
;
Ma,Wen Zhang
;
Choi,Seung Se
;
Hentschel,Jorn
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浏览/下载：104/34
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提交时间：2022/04/02
Ptilidium
cryptic speciation
evolution
Sino-Himalaya
taxonomy
MAXIMUM-LIKELIHOOD
UNIVERSAL PRIMERS
LEAFY LIVERWORT
AMPLIFICATION
SCAPANIACEAE
SPECIATION
TAXA
New Eocene fossil fruits and leaves of Menispermaceae from the central Tibetan Plateau and their biogeographic implications
期刊论文
JOURNAL OF SYSTEMATICS AND EVOLUTION, 2021, 卷号: 59, 期号: 6, 页码: 1287-1306
作者:
Del Rio,Cedric
;
Huang,Jian
;
Liu,Ping
;
Deng,Wei-Yu-Dong
;
Spicer,Teresa E. V.
;
Wu,Fei-Xiang
;
Zhou,Zhe-Kun
;
Su,Tao
Adobe PDF(9246Kb)
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浏览/下载：106/10
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提交时间：2022/04/02
endocarp
fossil plant
leaf
paleobotany
Tibetan Plateau
GENUS MENISPERMITES
LEAF-LITTER
PHYLOGENY
PALEOCENE
ENDOCARPS
PALEOGENE
FOREST
CLASSIFICATION
TRANSITION
VEGETATION
Snapshot of the Pliocene environment of West Kunlun region, Northwest China
期刊论文
PALAEOBIODIVERSITY AND PALAEOENVIRONMENTS, 2021, 卷号: 101, 期号: 1, 页码: 163-176
作者:
Liu,Jia
;
Wang,Teng-Xiang
;
Zhang,Xin-Wen
;
Song,Ai
;
Li,Shu-Feng
;
Huang,Jian
;
Spicer,Teresa
;
Spicer,Robert A.
;
Wu,Fei-Xiang
;
Su,Tao
;
Zhou,Zhe-Kun
Adobe PDF(13959Kb)
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浏览/下载：73/17
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提交时间：2022/04/02
Palynology
Stratigraphy
Tibetan Plateau
Tarim Basin
Aridification
Bimodal activity of diurnal flower visitation at high elevation
期刊论文
ECOLOGY AND EVOLUTION, 2021, 卷号: 11, 期号: 19, 页码: 13487-13500
作者:
Xu,Xin
;
Ren,Zong-Xin
;
Trunschke,Judith
;
Kuppler,Jonas
;
Zhao,Yan-Hui
;
Knop,Eva
;
Wang,Hong
Adobe PDF(903Kb)
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浏览/下载：86/37
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提交时间：2022/04/02
Bombus
diurnal activity patterns
flower visitors
high elevation
solar radiation
FALSE DISCOVERY RATE
ACTIVITY PATTERNS
SPATIOTEMPORAL VARIATION
POLLINATOR ACTIVITY
HYMENOPTERA APIDAE
SOLAR-RADIATION
BUMBLE BEES
COMMUNITY
ABUNDANCE
CLOCK
Evolutionary assembly of flowering plants into sky islands
期刊论文
NATURE ECOLOGY & EVOLUTION, 2021, 卷号: 5, 期号: 5, 页码: 640-646
作者:
Qian,Hong
;
Ricklefs,Robert E.
;
Thuiller,Wilfried
Adobe PDF(4034Kb)
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浏览/下载：48/11
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提交时间：2022/04/02
