×
验证码:
换一张
忘记密码？
记住我
×
登录
中文版
|
English
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
登录
注册
ALL
ORCID
题名
作者
学科领域
关键词
资助项目
文献类型
出处
收录类别
出版者
发表日期
存缴日期
学科门类
学习讨论厅
图片搜索
粘贴图片网址
首页
研究单元&专题
作者
文献类型
学科分类
知识图谱
新闻&公告
研究单元&专题
共享文献 [60]
中国科学院东亚植物... [36]
昆明植物所硕博研究... [23]
资源植物与生物技术... [17]
中国西南野生生物种质... [8]
云南省植物学会 [2]
更多...
作者
李德铢 [16]
许建初 [16]
孙航 [7]
赵琪 [5]
王红 [5]
yang jing [5]
更多...
文献类型
期刊论文 [129]
学位论文 [23]
专著 [16]
会议录 [1]
会议论文 [1]
发表日期
2021 [5]
2020 [14]
2019 [12]
2018 [9]
2017 [15]
2016 [10]
更多...
语种
英语 [98]
中文 [21]
出处
FUNGAL DI... [21]
Annals of ... [8]
TAXON [6]
Systematic... [5]
ANNALS OF ... [4]
MYCOSPHERE [4]
更多...
资助项目
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&field=eperson.unique.id&advanced=false&query1=herbaceous%2Bversus%2Bwoody%2Bspecies&&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":"Paphiopedilum and Cypripedium，known as slipper orchids in horticulture, belong to the subfamily Cypripedioideae of the Orchidaceae. Although they are closely related phylogenetically, there are significant differences in leaf traits and geographical distributions between two genera. This dissertation includes the following sections: (1) the leaf functional traits were compared in six species of the two genera; (2) the physiological responses of P. armeniacum to different water regimes, light regimes and low temperature; (3) the leaf phenotypic plastics of C. flavum in response to the different light condition and the photosynthetic characteristics of three Cypripedium species during sexual reproduction. The aims are to understand the convergent and divergent evolution between the two genera in leaf traits and their adaptive significances, and the leaf plastic responses to different levels of resources. Such information could provide scientific basis for conservation and domestication of Paphiopedilum and Cypripedium. The results are given below:1. Compared with Paphiopedilum, Cypripedium showed significantly higher photosynthetic rate (Pmax), leaf nitrogen content (Na), photosynthetic nitrogen utilization (PNUE), the fractions of leaf nitrogen partitioning in carboxylation (PC) and bioenergetics (PB), specific leaf area (SLA), ratio of leaf chlorophyll a and b (Chla/b), but significantly lower leaf construction cost (CC) and the ratio of leaf carbon content to leaf nitrogen (C/N). These leaf traits of Cypripedium are considered as the adaptation to short growing period and rich soil nutrients in the alpine habitats. Conversely, the long life span, low Pmax and mesophyll conductance (gm) but high SLA, CC and C/N in Paphiopedilum indicated that the adaptation to low-light, limited-nutrient habitat in the limestone area. As a sympatric species of Paphiopedilum, C. lentiginosum not only kept phylogenetically leaf traits of Cypripedium, suchas stomatal conductance (gs), Pmax, PNUE and dormant in winter, but also possessed many leaf traits which is similar to that in Paphiopedilum, such as relative stomatal limitations (RSL), gm, the ratio of leaf chlorophyll a and b (Chl a/b), fraction of leaf nitrogen allocated to light-harvesting components (PL). These results indicated the convergent and divergent evolution of Paphiopedilum and Cypripedium in leaf traits.2. Paphiopedilum. armeniacum exhibited a high plasticity of leaf photosynthetic function in response to different light regimes, but the responses changes with the time. Due to grow under low light habitat, P. armeniacum grown under 50% shade (HL) had the significantly lowest Pmax than the plants grown under 75% shade (ML) and 95% shade (LL) after six months. However, after twelve months, the Pmax of the plants grown under HL increased significantly and then became the highest one among three levels of light. It is also found that leaf dry mass per unit area (LMA), leaf stomatal conductance (gS), internal mesophyll conductance (gm), the fraction of leaf nitrogen partitioning in photosynthetic carboxylation (PC), bioeneretics (PB) were greatly influenced by irradiance. The plants grown under HL increased gS, gm, PC, PB to increase Pmax. In addition, the plants grown under HL had the highest ratio of total chlorophyll content to total Carotenoid content (Car/Chl) while the plants grown under LL had the lowest ratio of leaf chlorophyll a and b (Chl a/b). As a result, plasticity of leaf photosynthetic physiology of P. armeniacum in response to different light regimes depended largely on leaf nitrogen partitioning and leaf structure. As for the numbers of flowering and fruiting, ML was the best light level.3. The responses of P. armeniacum to different water regimes were not significantly different. But the Pmax and the maximum photochemical efficiency of PSⅡ (Fv/Fm) decreased with the increased frequency of watering. The reasons were that the plants have high respiration rate (Rd) and make more use of light energy to oxidation cycle. The plants watered every eight days (MW) and every twenty days (LW) had higher Pmax than the plant watered every four days (HW) mainly because of the higher PC and PB. Besides, the leaves of P. armeniacum had excellent property for holding water also contributed to the high photosynthetic capacity.4. Paphiopedilum. armeniacum was very sensitive to the low temperature. The plants significantly decreased photosynthetic capacity after grown under 4℃ for three days and the photosynthetic machinery was destroyed after fifteen days. The photosynthetic capacity of P. armeniacum exhibited no change at 10℃ and 15℃.5. Cypripedium flavum of four habitats (DB, XRD, XZD and TSQ) with different light intensity exhibited different photosynthetic characteristics after transplanted to the same environment in Kunming. Among the habitats, the light intensity of DB was the highest while XRD was the lowest. The light intensity of XZD and TSQ were not significantly difference. Among all the plants in Kunming, the plants of DB had the significantly highest Pmax but the plants of XRD had the lowest Pmax. The light saturation point (LSP) and photosynthetic nitrogen use efficiency (PNUE) agreed well with the light intensity of four habitats and contributed to the high Pmax of DB. The LMA, Chl and leaf nitrogen content were not different among all the plants. C. flavum exhibited sensitively response to the change of light in leaf construction while kept the plasticity of leaf photosynthetic characteristics which developed from its own habitat.6. The photosynthetic capacity of C. tibeticum and C. flavum were significantly increased at the flowering stage. For these two species, the significantly increased Amax were closely related to the maximum carboxylation rate by ribulose-1, 5-bisphosphate carboxylase/oxygenase (Vcmax), photon saturated rate of electron transport (Jmax), the rate of triose phosphate utilization (TPU) and actual quantum efficiency of the photosystem II photochemistry (ΦPSII) respectively. However, flowering almost did not affect the photosynthetic capacity of C. guttatum. C. guttatum had the smallest plant size, the leaf area, the volume of labellum and the volume of fruit, but the biggest fruit volume per leaf area among three species. These results indicated that for C. flavum and C. tibeticum there were a physiological mechanism in photosynthesis to compensate the cost of flowering as well as increased resource acquisitions, which would be beneficial to the survival or future flowering of the plant. C. gutattum could keep a steady photosynthetic capacity during life history. This kind of pattern could decrease the effect of the reproductive costs as much as possible. In contrast to C. flavum and C. tibeticum, C. gutattum possessed a more economical and effective reproductive pattern which maybe related to its wider distribution.In conclusion, Paphiopedilum and Cypripedium have significantly different leaf traits which agree well with their habitats and there is a divergent and convergent evolution between the two genera. P. armeniacum is much tolerant and responsive to varying water and light availability but very sensitivity to the low temperature. Confronting the suddenly change of light environment, C. flavum can respond sensitively to the change of light in leaf construction but the plasticity of leaf photosynthetic characteristics which developed from its own habitat can hold for the next growing season. In contrast to C. flavum and C. tibeticum, C. gutattum possesses a more economical and effective reproductive pattern which maybe related to its wider distribution. The study of the relationship between the two genera, the response and tolerance to the environmental factors of the two genera are important for understanding the adaptation and evolution of the Cypripedioideae.","jscount":"1","jsurl":"/simple-search?field1=all&field=eperson.unique.id&advanced=false&query1=herbaceous%2Bversus%2Bwoody%2Bspecies&&fq=dc.project.title_filter%3APaphiopedilum%5C+and%5C+Cypripedium%EF%BC%8Cknown%5C+as%5C+slipper%5C+orchids%5C+in%5C+horticulture%2C%5C+belong%5C+to%5C+the%5C+subfamily%5C+Cypripedioideae%5C+of%5C+the%5C+Orchidaceae.%5C+Although%5C+they%5C+are%5C+closely%5C+related%5C+phylogenetically%2C%5C+there%5C+are%5C+significant%5C+differences%5C+in%5C+leaf%5C+traits%5C+and%5C+geographical%5C+distributions%5C+between%5C+two%5C+genera.%5C+This%5C+dissertation%5C+includes%5C+the%5C+following%5C+sections%5C%3A%5C+%5C%281%5C%29%5C+the%5C+leaf%5C+functional%5C+traits%5C+were%5C+compared%5C+in%5C+six%5C+species%5C+of%5C+the%5C+two%5C+genera%5C%3B%5C+%5C%282%5C%29%5C+the%5C+physiological%5C+responses%5C+of%5C+P.%5C+armeniacum%5C+to%5C+different%5C+water%5C+regimes%2C%5C+light%5C+regimes%5C+and%5C+low%5C+temperature%5C%3B%5C+%5C%283%5C%29%5C+the%5C+leaf%5C+phenotypic%5C+plastics%5C+of%5C+C.%5C+flavum%5C+in%5C+response%5C+to%5C+the%5C+different%5C+light%5C+condition%5C+and%5C+the%5C+photosynthetic%5C+characteristics%5C+of%5C+three%5C+Cypripedium%5C+species%5C+during%5C+sexual%5C+reproduction.%5C+The%5C+aims%5C+are%5C+to%5C+understand%5C+the%5C+convergent%5C+and%5C+divergent%5C+evolution%5C+between%5C+the%5C+two%5C+genera%5C+in%5C+leaf%5C+traits%5C+and%5C+their%5C+adaptive%5C+significances%2C%5C+and%5C+the%5C+leaf%5C+plastic%5C+responses%5C+to%5C+different%5C+levels%5C+of%5C+resources.%5C+Such%5C+information%5C+could%5C+provide%5C+scientific%5C+basis%5C+for%5C+conservation%5C+and%5C+domestication%5C+of%5C+Paphiopedilum%5C+and%5C+Cypripedium.%5C+The%5C+results%5C+are%5C+given%5C+below%5C%3A1.%5C+Compared%5C+with%5C+Paphiopedilum%2C%5C+Cypripedium%5C+showed%5C+significantly%5C+higher%5C+photosynthetic%5C+rate%5C+%5C%28Pmax%5C%29%2C%5C+leaf%5C+nitrogen%5C+content%5C+%5C%28Na%5C%29%2C%5C+photosynthetic%5C+nitrogen%5C+utilization%5C+%5C%28PNUE%5C%29%2C%5C+the%5C+fractions%5C+of%5C+leaf%5C+nitrogen%5C+partitioning%5C+in%5C+carboxylation%5C+%5C%28PC%5C%29%5C+and%5C+bioenergetics%5C+%5C%28PB%5C%29%2C%5C+specific%5C+leaf%5C+area%5C+%5C%28SLA%5C%29%2C%5C+ratio%5C+of%5C+leaf%5C+chlorophyll%5C+a%5C+and%5C+b%5C+%5C%28Chla%5C%2Fb%5C%29%2C%5C+but%5C+significantly%5C+lower%5C+leaf%5C+construction%5C+cost%5C+%5C%28CC%5C%29%5C+and%5C+the%5C+ratio%5C+of%5C+leaf%5C+carbon%5C+content%5C+to%5C+leaf%5C+nitrogen%5C+%5C%28C%5C%2FN%5C%29.%5C+These%5C+leaf%5C+traits%5C+of%5C+Cypripedium%5C+are%5C+considered%5C+as%5C+the%5C+adaptation%5C+to%5C+short%5C+growing%5C+period%5C+and%5C+rich%5C+soil%5C+nutrients%5C+in%5C+the%5C+alpine%5C+habitats.%5C+Conversely%2C%5C+the%5C+long%5C+life%5C+span%2C%5C+low%5C+Pmax%5C+and%5C+mesophyll%5C+conductance%5C+%5C%28gm%5C%29%5C+but%5C+high%5C+SLA%2C%5C+CC%5C+and%5C+C%5C%2FN%5C+in%5C+Paphiopedilum%5C+indicated%5C+that%5C+the%5C+adaptation%5C+to%5C+low%5C-light%2C%5C+limited%5C-nutrient%5C+habitat%5C+in%5C+the%5C+limestone%5C+area.%5C+As%5C+a%5C+sympatric%5C+species%5C+of%5C+Paphiopedilum%2C%5C+C.%5C+lentiginosum%5C+not%5C+only%5C+kept%5C+phylogenetically%5C+leaf%5C+traits%5C+of%5C+Cypripedium%2C%5C+suchas%5C+stomatal%5C+conductance%5C+%5C%28gs%5C%29%2C%5C+Pmax%2C%5C+PNUE%5C+and%5C+dormant%5C+in%5C+winter%2C%5C+but%5C+also%5C+possessed%5C+many%5C+leaf%5C+traits%5C+which%5C+is%5C+similar%5C+to%5C+that%5C+in%5C+Paphiopedilum%2C%5C+such%5C+as%5C+relative%5C+stomatal%5C+limitations%5C+%5C%28RSL%5C%29%2C%5C+gm%2C%5C+the%5C+ratio%5C+of%5C+leaf%5C+chlorophyll%5C+a%5C+and%5C+b%5C+%5C%28Chl%5C+a%5C%2Fb%5C%29%2C%5C+fraction%5C+of%5C+leaf%5C+nitrogen%5C+allocated%5C+to%5C+light%5C-harvesting%5C+components%5C+%5C%28PL%5C%29.%5C+These%5C+results%5C+indicated%5C+the%5C+convergent%5C+and%5C+divergent%5C+evolution%5C+of%5C+Paphiopedilum%5C+and%5C+Cypripedium%5C+in%5C+leaf%5C+traits.2.%5C+Paphiopedilum.%5C+armeniacum%5C+exhibited%5C+a%5C+high%5C+plasticity%5C+of%5C+leaf%5C+photosynthetic%5C+function%5C+in%5C+response%5C+to%5C+different%5C+light%5C+regimes%2C%5C+but%5C+the%5C+responses%5C+changes%5C+with%5C+the%5C+time.%5C+Due%5C+to%5C+grow%5C+under%5C+low%5C+light%5C+habitat%2C%5C+P.%5C+armeniacum%5C+grown%5C+under%5C+50%25%5C+shade%5C+%5C%28HL%5C%29%5C+had%5C+the%5C+significantly%5C+lowest%5C+Pmax%5C+than%5C+the%5C+plants%5C+grown%5C+under%5C+75%25%5C+shade%5C+%5C%28ML%5C%29%5C+and%5C+95%25%5C+shade%5C+%5C%28LL%5C%29%5C+after%5C+six%5C+months.%5C+However%2C%5C+after%5C+twelve%5C+months%2C%5C+the%5C+Pmax%5C+of%5C+the%5C+plants%5C+grown%5C+under%5C+HL%5C+increased%5C+significantly%5C+and%5C+then%5C+became%5C+the%5C+highest%5C+one%5C+among%5C+three%5C+levels%5C+of%5C+light.%5C+It%5C+is%5C+also%5C+found%5C+that%5C+leaf%5C+dry%5C+mass%5C+per%5C+unit%5C+area%5C+%5C%28LMA%5C%29%2C%5C+leaf%5C+stomatal%5C+conductance%5C+%5C%28gS%5C%29%2C%5C+internal%5C+mesophyll%5C+conductance%5C+%5C%28gm%5C%29%2C%5C+the%5C+fraction%5C+of%5C+leaf%5C+nitrogen%5C+partitioning%5C+in%5C+photosynthetic%5C+carboxylation%5C+%5C%28PC%5C%29%2C%5C+bioeneretics%5C+%5C%28PB%5C%29%5C+were%5C+greatly%5C+influenced%5C+by%5C+irradiance.%5C+The%5C+plants%5C+grown%5C+under%5C+HL%5C+increased%5C+gS%2C%5C+gm%2C%5C+PC%2C%5C+PB%5C+to%5C+increase%5C+Pmax.%5C+In%5C+addition%2C%5C+the%5C+plants%5C+grown%5C+under%5C+HL%5C+had%5C+the%5C+highest%5C+ratio%5C+of%5C+total%5C+chlorophyll%5C+content%5C+to%5C+total%5C+Carotenoid%5C+content%5C+%5C%28Car%5C%2FChl%5C%29%5C+while%5C+the%5C+plants%5C+grown%5C+under%5C+LL%5C+had%5C+the%5C+lowest%5C+ratio%5C+of%5C+leaf%5C+chlorophyll%5C+a%5C+and%5C+b%5C+%5C%28Chl%5C+a%5C%2Fb%5C%29.%5C+As%5C+a%5C+result%2C%5C+plasticity%5C+of%5C+leaf%5C+photosynthetic%5C+physiology%5C+of%5C+P.%5C+armeniacum%5C+in%5C+response%5C+to%5C+different%5C+light%5C+regimes%5C+depended%5C+largely%5C+on%5C+leaf%5C+nitrogen%5C+partitioning%5C+and%5C+leaf%5C+structure.%5C+As%5C+for%5C+the%5C+numbers%5C+of%5C+flowering%5C+and%5C+fruiting%2C%5C+ML%5C+was%5C+the%5C+best%5C+light%5C+level.3.%5C+The%5C+responses%5C+of%5C+P.%5C+armeniacum%5C+to%5C+different%5C+water%5C+regimes%5C+were%5C+not%5C+significantly%5C+different.%5C+But%5C+the%5C+Pmax%5C+and%5C+the%5C+maximum%5C+photochemical%5C+efficiency%5C+of%5C+PS%E2%85%A1%5C+%5C%28Fv%5C%2FFm%5C%29%5C+decreased%5C+with%5C+the%5C+increased%5C+frequency%5C+of%5C+watering.%5C+The%5C+reasons%5C+were%5C+that%5C+the%5C+plants%5C+have%5C+high%5C+respiration%5C+rate%5C+%5C%28Rd%5C%29%5C+and%5C+make%5C+more%5C+use%5C+of%5C+light%5C+energy%5C+to%5C+oxidation%5C+cycle.%5C+The%5C+plants%5C+watered%5C+every%5C+eight%5C+days%5C+%5C%28MW%5C%29%5C+and%5C+every%5C+twenty%5C+days%5C+%5C%28LW%5C%29%5C+had%5C+higher%5C+Pmax%5C+than%5C+the%5C+plant%5C+watered%5C+every%5C+four%5C+days%5C+%5C%28HW%5C%29%5C+mainly%5C+because%5C+of%5C+the%5C+higher%5C+PC%5C+and%5C+PB.%5C+Besides%2C%5C+the%5C+leaves%5C+of%5C+P.%5C+armeniacum%5C+had%5C+excellent%5C+property%5C+for%5C+holding%5C+water%5C+also%5C+contributed%5C+to%5C+the%5C+high%5C+photosynthetic%5C+capacity.4.%5C+Paphiopedilum.%5C+armeniacum%5C+was%5C+very%5C+sensitive%5C+to%5C+the%5C+low%5C+temperature.%5C+The%5C+plants%5C+significantly%5C+decreased%5C+photosynthetic%5C+capacity%5C+after%5C+grown%5C+under%5C+4%E2%84%83%5C+for%5C+three%5C+days%5C+and%5C+the%5C+photosynthetic%5C+machinery%5C+was%5C+destroyed%5C+after%5C+fifteen%5C+days.%5C+The%5C+photosynthetic%5C+capacity%5C+of%5C+P.%5C+armeniacum%5C+exhibited%5C+no%5C+change%5C+at%5C+10%E2%84%83%5C+and%5C+15%E2%84%83.5.%5C+Cypripedium%5C+flavum%5C+of%5C+four%5C+habitats%5C+%5C%28DB%2C%5C+XRD%2C%5C+XZD%5C+and%5C+TSQ%5C%29%5C+with%5C+different%5C+light%5C+intensity%5C+exhibited%5C+different%5C+photosynthetic%5C+characteristics%5C+after%5C+transplanted%5C+to%5C+the%5C+same%5C+environment%5C+in%5C+Kunming.%5C+Among%5C+the%5C+habitats%2C%5C+the%5C+light%5C+intensity%5C+of%5C+DB%5C+was%5C+the%5C+highest%5C+while%5C+XRD%5C+was%5C+the%5C+lowest.%5C+The%5C+light%5C+intensity%5C+of%5C+XZD%5C+and%5C+TSQ%5C+were%5C+not%5C+significantly%5C+difference.%5C+Among%5C+all%5C+the%5C+plants%5C+in%5C+Kunming%2C%5C+the%5C+plants%5C+of%5C+DB%5C+had%5C+the%5C+significantly%5C+highest%5C+Pmax%5C+but%5C+the%5C+plants%5C+of%5C+XRD%5C+had%5C+the%5C+lowest%5C+Pmax.%5C+The%5C+light%5C+saturation%5C+point%5C+%5C%28LSP%5C%29%5C+and%5C+photosynthetic%5C+nitrogen%5C+use%5C+efficiency%5C+%5C%28PNUE%5C%29%5C+agreed%5C+well%5C+with%5C+the%5C+light%5C+intensity%5C+of%5C+four%5C+habitats%5C+and%5C+contributed%5C+to%5C+the%5C+high%5C+Pmax%5C+of%5C+DB.%5C+The%5C+LMA%2C%5C+Chl%5C+and%5C+leaf%5C+nitrogen%5C+content%5C+were%5C+not%5C+different%5C+among%5C+all%5C+the%5C+plants.%5C+C.%5C+flavum%5C+exhibited%5C+sensitively%5C+response%5C+to%5C+the%5C+change%5C+of%5C+light%5C+in%5C+leaf%5C+construction%5C+while%5C+kept%5C+the%5C+plasticity%5C+of%5C+leaf%5C+photosynthetic%5C+characteristics%5C+which%5C+developed%5C+from%5C+its%5C+own%5C+habitat.6.%5C+The%5C+photosynthetic%5C+capacity%5C+of%5C+C.%5C+tibeticum%5C+and%5C+C.%5C+flavum%5C+were%5C+significantly%5C+increased%5C+at%5C+the%5C+flowering%5C+stage.%5C+For%5C+these%5C+two%5C+species%2C%5C+the%5C+significantly%5C+increased%5C+Amax%5C+were%5C+closely%5C+related%5C+to%5C+the%5C+maximum%5C+carboxylation%5C+rate%5C+by%5C+ribulose%5C-1%2C%5C+5%5C-bisphosphate%5C+carboxylase%5C%2Foxygenase%5C+%5C%28Vcmax%5C%29%2C%5C+photon%5C+saturated%5C+rate%5C+of%5C+electron%5C+transport%5C+%5C%28Jmax%5C%29%2C%5C+the%5C+rate%5C+of%5C+triose%5C+phosphate%5C+utilization%5C+%5C%28TPU%5C%29%5C+and%5C+actual%5C+quantum%5C+efficiency%5C+of%5C+the%5C+photosystem%5C+II%5C+photochemistry%5C+%5C%28%CE%A6PSII%5C%29%5C+respectively.%5C+However%2C%5C+flowering%5C+almost%5C+did%5C+not%5C+affect%5C+the%5C+photosynthetic%5C+capacity%5C+of%5C+C.%5C+guttatum.%5C+C.%5C+guttatum%5C+had%5C+the%5C+smallest%5C+plant%5C+size%2C%5C+the%5C+leaf%5C+area%2C%5C+the%5C+volume%5C+of%5C+labellum%5C+and%5C+the%5C+volume%5C+of%5C+fruit%2C%5C+but%5C+the%5C+biggest%5C+fruit%5C+volume%5C+per%5C+leaf%5C+area%5C+among%5C+three%5C+species.%5C+These%5C+results%5C+indicated%5C+that%5C+for%5C+C.%5C+flavum%5C+and%5C+C.%5C+tibeticum%5C+there%5C+were%5C+a%5C+physiological%5C+mechanism%5C+in%5C+photosynthesis%5C+to%5C+compensate%5C+the%5C+cost%5C+of%5C+flowering%5C+as%5C+well%5C+as%5C+increased%5C+resource%5C+acquisitions%2C%5C+which%5C+would%5C+be%5C+beneficial%5C+to%5C+the%5C+survival%5C+or%5C+future%5C+flowering%5C+of%5C+the%5C+plant.%5C+C.%5C+gutattum%5C+could%5C+keep%5C+a%5C+steady%5C+photosynthetic%5C+capacity%5C+during%5C+life%5C+history.%5C+This%5C+kind%5C+of%5C+pattern%5C+could%5C+decrease%5C+the%5C+effect%5C+of%5C+the%5C+reproductive%5C+costs%5C+as%5C+much%5C+as%5C+possible.%5C+In%5C+contrast%5C+to%5C+C.%5C+flavum%5C+and%5C+C.%5C+tibeticum%2C%5C+C.%5C+gutattum%5C+possessed%5C+a%5C+more%5C+economical%5C+and%5C+effective%5C+reproductive%5C+pattern%5C+which%5C+maybe%5C+related%5C+to%5C+its%5C+wider%5C+distribution.In%5C+conclusion%2C%5C+Paphiopedilum%5C+and%5C+Cypripedium%5C+have%5C+significantly%5C+different%5C+leaf%5C+traits%5C+which%5C+agree%5C+well%5C+with%5C+their%5C+habitats%5C+and%5C+there%5C+is%5C+a%5C+divergent%5C+and%5C+convergent%5C+evolution%5C+between%5C+the%5C+two%5C+genera.%5C+P.%5C+armeniacum%5C+is%5C+much%5C+tolerant%5C+and%5C+responsive%5C+to%5C+varying%5C+water%5C+and%5C+light%5C+availability%5C+but%5C+very%5C+sensitivity%5C+to%5C+the%5C+low%5C+temperature.%5C+Confronting%5C+the%5C+suddenly%5C+change%5C+of%5C+light%5C+environment%2C%5C+C.%5C+flavum%5C+can%5C+respond%5C+sensitively%5C+to%5C+the%5C+change%5C+of%5C+light%5C+in%5C+leaf%5C+construction%5C+but%5C+the%5C+plasticity%5C+of%5C+leaf%5C+photosynthetic%5C+characteristics%5C+which%5C+developed%5C+from%5C+its%5C+own%5C+habitat%5C+can%5C+hold%5C+for%5C+the%5C+next%5C+growing%5C+season.%5C+In%5C+contrast%5C+to%5C+C.%5C+flavum%5C+and%5C+C.%5C+tibeticum%2C%5C+C.%5C+gutattum%5C+possesses%5C+a%5C+more%5C+economical%5C+and%5C+effective%5C+reproductive%5C+pattern%5C+which%5C+maybe%5C+related%5C+to%5C+its%5C+wider%5C+distribution.%5C+The%5C+study%5C+of%5C+the%5C+relationship%5C+between%5C+the%5C+two%5C+genera%2C%5C+the%5C+response%5C+and%5C+tolerance%5C+to%5C+the%5C+environmental%5C+factors%5C+of%5C+the%5C+two%5C+genera%5C+are%5C+important%5C+for%5C+understanding%5C+the%5C+adaptation%5C+and%5C+evolution%5C+of%5C+the%5C+Cypripedioideae."},{"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&field=eperson.unique.id&advanced=false&query1=herbaceous%2Bversus%2Bwoody%2Bspecies&&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":"Program of Science and Technology Talents Training of Yunnan Province[2017HA014]","jscount":"1","jsurl":"/simple-search?field1=all&field=eperson.unique.id&advanced=false&query1=herbaceous%2Bversus%2Bwoody%2Bspecies&&fq=dc.project.title_filter%3AProgram%5C+of%5C+Science%5C+and%5C+Technology%5C+Talents%5C+Training%5C+of%5C+Yunnan%5C+Province%5C%5B2017HA014%5C%5D"},{"jsname":"Projects of International Cooperation and Exchanges, NSFC[41661144001]","jscount":"1","jsurl":"/simple-search?field1=all&field=eperson.unique.id&advanced=false&query1=herbaceous%2Bversus%2Bwoody%2Bspecies&&fq=dc.project.title_filter%3AProjects%5C+of%5C+International%5C+Cooperation%5C+and%5C+Exchanges%2C%5C+NSFC%5C%5B41661144001%5C%5D"},{"jsname":"Provincial Innovation Group for Farmland Non-pollution Production, Yunnan Agricultural University[2017HC015]","jscount":"1","jsurl":"/simple-search?field1=all&field=eperson.unique.id&advanced=false&query1=herbaceous%2Bversus%2Bwoody%2Bspecies&&fq=dc.project.title_filter%3AProvincial%5C+Innovation%5C+Group%5C+for%5C+Farmland%5C+Non%5C-pollution%5C+Production%2C%5C+Yunnan%5C+Agricultural%5C+University%5C%5B2017HC015%5C%5D"},{"jsname":"Scottish Government''s Rural and Environmental Science and Analytical Services Division","jscount":"1","jsurl":"/simple-search?field1=all&field=eperson.unique.id&advanced=false&query1=herbaceous%2Bversus%2Bwoody%2Bspecies&&fq=dc.project.title_filter%3AScottish%5C+Government%27%27s%5C+Rural%5C+and%5C+Environmental%5C+Science%5C+and%5C+Analytical%5C+Services%5C+Division"},{"jsname":"The temperate woody bamboos are a morphologically diverse group with a complicated taxonomy. The Arundinaria group has an East Asia-North America disjunct distribution, which is one of those with complex taxonomy in the temperate woody bamboos. In this study, the phylogeny of the temperate woody bamboos was reconstructed based on eight non-coding regions of the chloroplast genome and nuclear gene GBSSI using large sample set (124 species in 24 genera) with an emphasis on the Arundinaria group. The monophyly of the temperate woody bamboos was resolved in all phylogenies. Ten major lineages were obtained in the chloroplast phylogeny with unresolved relationships among them; the recovered phylogeny is strongly incongruent with the classifications based on morphology at both subtribal and generic ranks; some subclades that are related to the geographic distribution were obtained in those lineages. Five lineages in the GBSSI gene phylogeny were recovered as the same in the chloroplast phylogeny, and the other lineages were incongruent with chloroplast phylogeny in some ways. The reticulate evolution caused by hybridization, introgression and lineage sorting may be an explanation for the molecular phylogenetic incongruence. Based on the facts of diverse morphology, broad distribution and molecular phylogeny, we inferred that the major clades and species within most of the clades of the temperate woody bamboos were originated during several rapid adaptive radiations. Ten putative hybrids were discussed based on molecular phylogenies, morphology and distribution. The micromorphology of the leaf epidermis under SEM (scanning electron microscope) was observed and divided into nine types; the micromorphology can provide some evidence for the bamboo taxonomy and inference of putative hybrids. Additionally, taxonomic revisions were presented for some species based on field observation and herbarium work.","jscount":"1","jsurl":"/simple-search?field1=all&field=eperson.unique.id&advanced=false&query1=herbaceous%2Bversus%2Bwoody%2Bspecies&&fq=dc.project.title_filter%3AThe%5C+temperate%5C+woody%5C+bamboos%5C+are%5C+a%5C+morphologically%5C+diverse%5C+group%5C+with%5C+a%5C+complicated%5C+taxonomy.%5C+The%5C+Arundinaria%5C+group%5C+has%5C+an%5C+East%5C+Asia%5C-North%5C+America%5C+disjunct%5C+distribution%2C%5C+which%5C+is%5C+one%5C+of%5C+those%5C+with%5C+complex%5C+taxonomy%5C+in%5C+the%5C+temperate%5C+woody%5C+bamboos.%5C+In%5C+this%5C+study%2C%5C+the%5C+phylogeny%5C+of%5C+the%5C+temperate%5C+woody%5C+bamboos%5C+was%5C+reconstructed%5C+based%5C+on%5C+eight%5C+non%5C-coding%5C+regions%5C+of%5C+the%5C+chloroplast%5C+genome%5C+and%5C+nuclear%5C+gene%5C+GBSSI%5C+using%5C+large%5C+sample%5C+set%5C+%5C%28124%5C+species%5C+in%5C+24%5C+genera%5C%29%5C+with%5C+an%5C+emphasis%5C+on%5C+the%5C+Arundinaria%5C+group.%5C+The%5C+monophyly%5C+of%5C+the%5C+temperate%5C+woody%5C+bamboos%5C+was%5C+resolved%5C+in%5C+all%5C+phylogenies.%5C+Ten%5C+major%5C+lineages%5C+were%5C+obtained%5C+in%5C+the%5C+chloroplast%5C+phylogeny%5C+with%5C+unresolved%5C+relationships%5C+among%5C+them%5C%3B%5C+the%5C+recovered%5C+phylogeny%5C+is%5C+strongly%5C+incongruent%5C+with%5C+the%5C+classifications%5C+based%5C+on%5C+morphology%5C+at%5C+both%5C+subtribal%5C+and%5C+generic%5C+ranks%5C%3B%5C+some%5C+subclades%5C+that%5C+are%5C+related%5C+to%5C+the%5C+geographic%5C+distribution%5C+were%5C+obtained%5C+in%5C+those%5C+lineages.%5C+Five%5C+lineages%5C+in%5C+the%5C+GBSSI%5C+gene%5C+phylogeny%5C+were%5C+recovered%5C+as%5C+the%5C+same%5C+in%5C+the%5C+chloroplast%5C+phylogeny%2C%5C+and%5C+the%5C+other%5C+lineages%5C+were%5C+incongruent%5C+with%5C+chloroplast%5C+phylogeny%5C+in%5C+some%5C+ways.%5C+The%5C+reticulate%5C+evolution%5C+caused%5C+by%5C+hybridization%2C%5C+introgression%5C+and%5C+lineage%5C+sorting%5C+may%5C+be%5C+an%5C+explanation%5C+for%5C+the%5C+molecular%5C+phylogenetic%5C+incongruence.%5C+Based%5C+on%5C+the%5C+facts%5C+of%5C+diverse%5C+morphology%2C%5C+broad%5C+distribution%5C+and%5C+molecular%5C+phylogeny%2C%5C+we%5C+inferred%5C+that%5C+the%5C+major%5C+clades%5C+and%5C+species%5C+within%5C+most%5C+of%5C+the%5C+clades%5C+of%5C+the%5C+temperate%5C+woody%5C+bamboos%5C+were%5C+originated%5C+during%5C+several%5C+rapid%5C+adaptive%5C+radiations.%5C+Ten%5C+putative%5C+hybrids%5C+were%5C+discussed%5C+based%5C+on%5C+molecular%5C+phylogenies%2C%5C+morphology%5C+and%5C+distribution.%5C+The%5C+micromorphology%5C+of%5C+the%5C+leaf%5C+epidermis%5C+under%5C+SEM%5C+%5C%28scanning%5C+electron%5C+microscope%5C%29%5C+was%5C+observed%5C+and%5C+divided%5C+into%5C+nine%5C+types%5C%3B%5C+the%5C+micromorphology%5C+can%5C+provide%5C+some%5C+evidence%5C+for%5C+the%5C+bamboo%5C+taxonomy%5C+and%5C+inference%5C+of%5C+putative%5C+hybrids.%5C+Additionally%2C%5C+taxonomic%5C+revisions%5C+were%5C+presented%5C+for%5C+some%5C+species%5C+based%5C+on%5C+field%5C+observation%5C+and%5C+herbarium%5C+work."},{"jsname":"Yunnan Postdoctoral Science Foundation[Y732081261]","jscount":"1","jsurl":"/simple-search?field1=all&field=eperson.unique.id&advanced=false&query1=herbaceous%2Bversus%2Bwoody%2Bspecies&&fq=dc.project.title_filter%3AYunnan%5C+Postdoctoral%5C+Science%5C+Foundation%5C%5BY732081261%5C%5D"},{"jsname":"lastIndexed","jscount":"2024-04-15"}],"资助项目","dc.project.title_filter")'>
National K... [2]
Bambusoide... [1]
Federal Mi... [1]
Fundamenta... [1]
Keynote Pr... [1]
Large-scal... [1]
更多...
收录类别
SCI [63]
CSCD [2]
SSCI [1]
资助机构
Chinese Ac... [5]
Deanship o... [3]
Biosystems... [2]
CAS/SAFEA ... [2]
John D. an... [2]
MFLU(56101... [2]
更多...
×
知识图谱
KIB OpenIR
开始提交
已提交作品
待认领作品
已认领作品
未提交全文
收藏管理
QQ客服
官方微博
反馈留言
分面浏览：作者
当前检索式
((ALL：herbaceous versus woody species))
限定条件
无
共44条，第1-20条
李德铢
16
许建初
16
孙航
7
赵琪
5
王红
5
yang jing
5
郭振华
4
高连明
4
刘杰
3
周浙昆
3
邓涛
3
张宪智
2
杨杨
2
伊廷双
2
杨祝良
2
胡虹
2
张石宝
2
张韵洁
2
向春雷
2
张建文
1
