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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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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 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Research Fund (TRF)[RSA5980068]","jscount":"1","jsurl":"/simple-search?field1=all&rpp=10&accurate=false&advanced=false&sort_by=2&isNonaffiliated=false&search_type=-1&query1=QUERCUS-ROBUR&order=desc&&fq=dc.project.title_filter%3AThailand%5C+Research%5C+Fund%5C+%5C%28TRF%5C%29%5C%5BRSA5980068%5C%5D"},{"jsname":"The genus Quercus consists of subgenera Quercus and Cyclobalanopsis and has approximately 531 species, making this the largest and most widely distributed genus within the Fagaceae family, occurring throughout temperate and subtropical montane areas of the Northern Hemisphere. The occurrence of recalcitrant (desiccation-sensitive) seeded plants is common in the genus Quercus, making it one of the key genera for understanding the physiology and the ecology of recalcitrant seeds. Due to habitat loss and poor regeneration, some populations of the genus Quercus are now declining. Moreover, the limited availability of good-quality seed may lead to its natural regeneration problems. To understand the cause of the population decline and to conserve iteffectively, knowledge on the seed/fruit biology of Quercus is necessary. Despite this, the seed/fruit biology of the Asian Quercus species is largely overlooked and the seed/fruit biology of Quercus subgenus Cyclobalanopsis,which is predominately distributed across tropical and subtropical Asia, is less well documented. To provide new data on the fruit biology of subgenus Cyclobalanopsis and to understand the fruit physiology and ecology of the genus Quercus comprehensively for a conservation aim, the germination and desiccation response of 11 species of subgenus Cyclobalanopsis (from S and SW China) and 11 species of subgenus Quercus (from both SW China and Europe) were investigated. The anatomic characteristics of the fruit coats was analysed on 9 of these species and the oil contents were quantified from 18 of these species. In addition, a study was carried out over 4 years on the fruit production of Q. schottkyana (subgenus Cyclobalanopsis) to fill the gap in knowledge. The data demonstrate that: 1. All 22 species of subgenus Cyclobalanopsis and subgenus Quercus had desiccation-sensitive (recalcitrant) fruits. For these 22 species which had fruit dry masses spanning 0.57 to 6.41 g and seed coat ratios spanning 0.15 to 0.48, there were wide differences in drying rates (0.26-4.10 %d-1). These differences were independent of fruit mass and seed coat ratio, but were related to the morphology of the fruit coat.2. The scar, composing 4% to 37% (surface area) of the whole fruit coat, was found to be the main water passage for most species. Water transferred directly and quickly through the scar. From the scar through to the pericarp and ending at the apex, there was a longitudinal passage of water flow. The anatomic characteristics of the fruit coats controlled the water flux, which furthermore introduced the wide differences in drying rates between the Quercus species.3. In comparison to species of Quercus subgenus Quercus, fruits in subgenus Cyclobalanopsis germinated faster and most had maximum germination at the highest temperature of 25°C. At lower temperatures (15°C, 20°C), germination of subgenus Cyclobalanopsis was slower and the germination percentage of most species was decreased, but germination of species in subgenus Quercus was not affected at these low temperatures. The thermal requirements for the germination of these two subgenera suggested an adaptability of these fruits to their habitats.4. Fruit oil content of subgenus Cyclobalanopsis (0.70% to 3.77%) was significantly lower than that of subgenus Quercus (1.48 to 18.01%) and across the 18 species studied, moisture content of the storage tissue (cotyledons) was negatively related to fruit oil content. These data were combined with that from the literature, resulting in a total of 57 species, and mapped against the current phylogeny for Quercus to reveal the highest fruit oil contents associated with sect. Lobatae. 5. The fruit production of Q. schottkyana varied markedly between years. Each square meter of Q. schottkyana pure forest produced 245-854 fruits but 14%-48% of them were infected by weevils (Curculio sp.). The annual production of Q. schottkyana was most likely affected by the average monthly rainfall during May and June, but the time of fruit dispersal was related to the rainfall of September and November. The infestation rates of weevils were density-dependent on the fruit production of Q. schottkyana that furthermore regulated the populations of these two 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doichangensis is an endangered plant. In this paper, the megasporogenesis and development of female gametophyte, seed morphological traits and seed germination, seed conservation, micropropagation and acclimatization of this species were studied. Combined with the published results of cytology, molecular genetics and other researches,the mechanisms of extinction, basic biology and technology of germplasm conservation and acclimatization of T. doichangensis were discussed. The main results are summarized as follows:1. Megasporogenesis and development of female gametophyte，Stamens exist under the stigma of T. doichangensis, and the pollen is aborted on the later development stage of pistil, therefore, the pistillate flower in function is hermaphrodite flower in morphology. The ovule is anatropous, bitegmic and crassinucellate. The primary archesporium is hypodermal and single-celled and the sporogenous cell of the nucellus functions directly as a megaspore mother cell which goes meiosis to form a linear tetrad. The chalazal megaspore of the tetrad is functional. The development of embryo sac conforms to the polygonum type. There are six ovules in the ovary of T. doichangensis, and only one develops into a seed in normal fruits. In the process of megasporogenesis and development of female gametophyte, there are several links of abortion, and 93.3% of mature embryo sacs is aborted.2. Morphological characters and germination of seeds，Most of the variation occurred among individual trees within populations in seed morphological traits (length, width and 1000-seed weight) and germination-related indices (germination percentage, germination index and vigor index). In addition, the variation in percentage of well-developed seeds among populations and among individual trees within populations is equal, each accounting for 48%. Each of seed morphological traits has significantly positive correlation with each other (p < 0.01), but they have no significant correlation with percentage of well-developed seeds and germination-related indices. In the same batch of seeds of T. doichangensis, there are light-colored and dark-colored seed coats, and development of light-colored seeds is significantly poorer than that of dark-colored seeds.The sensitivity of seeds to high temperature varys in different stages of seed imbibition. In each stage, heat acclimatization don’t increase germination percentage, germination index and fresh weight of seedlings. If the distilled water is substituted by solution of SA during seed imbibition, seed germination and germination index after heat shock are not significantly different from control, but they are significantly higher than that of other treatments. Moreover, when the seeds are treatmented with SA, the fresh weight of seedlings is significantly higher than that of control and other treatments.3. Seed conservation，Seeds of T. doichangensis belong to orthodox seeds which can tolerate certain level of dehydration. The condition of low temperature and low water content of seeds is conducive to seed conservation.Germination of fresh seeds shows significant variation among populations, howerer, germination of the seeds after storage for one year in room temperature shows no significant variation among populations.High temperature and high relative humidity damages the seeds more severely than high temperature does. In addition, low water content of seeds enable the seeds to be more tolerant to high temperature.The electrical conductivity, dehydrogenase activity and germination percentage have no significant correlation with each other.4. Micropropagation and in vitro conservation，Cotyledonary nodes are a kind of efficient explants. Low salt media are conducive to shoot propagation and root induction.The maximum multiplication rate (20-25 shoots/explant within 4 months) is achieved on quarter-strength Murashige and Skoog (1/4 MS) medium supplemented with 1 mg·L-1 6-benzyladenine (6-BA) and 0.05 mg·L-1 α-naphthaleneacetic acid (NAA).Rooting is promoted by auxins, however, IBA alone or low concentrations of NAA are preferable due to small amount of callus induced. The research has established an efficient protocol for micropropagation of T. doichangensis, and it provides technology support for in vitro conservation of special germplasm of the species.5. Acclimatization，Quercus variabilis, Cyclobalanopsis glaucoides and T. doichangensis belong to the family of Fagaceae, and the natural distribution ranges of the 3 species are decreasing in turn. The research suggests that the ranges of temperature tolerance of the 3 species are decreasing corresponding to their distribution ranges.The high and low semi-lethal temperature of one-year old T. doichangensis is 49.5℃ and -5℃ respectively. It suggests that T. doichangensis has a wide range of basic temperature tolerance. Short-term heat and cold acclimatization cannot expand the range of temperature tolerance. It can be inferred that T. doichangensis may lack induced tolerance to temperature. Under proper conditions, ABA can increase the cold tolerance, and SA can increase the heat tolerance of leaf discs of T. doichangensis.","jscount":"1","jsurl":"/simple-search?field1=all&rpp=10&accurate=false&advanced=false&sort_by=2&isNonaffiliated=false&search_type=-1&query1=QUERCUS-ROBUR&order=desc&&fq=dc.project.title_filter%3ATrigonobalanus%5C+doichangensis%5C+is%5C+an%5C+endangered%5C+plant.%5C+In%5C+this%5C+paper%2C%5C+the%5C+megasporogenesis%5C+and%5C+development%5C+of%5C+female%5C+gametophyte%2C%5C+seed%5C+morphological%5C+traits%5C+and%5C+seed%5C+germination%2C%5C+seed%5C+conservation%2C%5C+micropropagation%5C+and%5C+acclimatization%5C+of%5C+this%5C+species%5C+were%5C+studied.%5C+Combined%5C+with%5C+the%5C+published%5C+results%5C+of%5C+cytology%2C%5C+molecular%5C+genetics%5C+and%5C+other%5C+researches%2Cthe%5C+mechanisms%5C+of%5C+extinction%2C%5C+basic%5C+biology%5C+and%5C+technology%5C+of%5C+germplasm%5C+conservation%5C+and%5C+acclimatization%5C+of%5C+T.%5C+doichangensis%5C+were%5C+discussed.%5C+The%5C+main%5C+results%5C+are%5C+summarized%5C+as%5C+follows%5C%3A1.%5C+Megasporogenesis%5C+and%5C+development%5C+of%5C+female%5C+gametophyte%EF%BC%8CStamens%5C+exist%5C+under%5C+the%5C+stigma%5C+of%5C+T.%5C+doichangensis%2C%5C+and%5C+the%5C+pollen%5C+is%5C+aborted%5C+on%5C+the%5C+later%5C+development%5C+stage%5C+of%5C+pistil%2C%5C+therefore%2C%5C+the%5C+pistillate%5C+flower%5C+in%5C+function%5C+is%5C+hermaphrodite%5C+flower%5C+in%5C+morphology.%5C+The%5C+ovule%5C+is%5C+anatropous%2C%5C+bitegmic%5C+and%5C+crassinucellate.%5C+The%5C+primary%5C+archesporium%5C+is%5C+hypodermal%5C+and%5C+single%5C-celled%5C+and%5C+the%5C+sporogenous%5C+cell%5C+of%5C+the%5C+nucellus%5C+functions%5C+directly%5C+as%5C+a%5C+megaspore%5C+mother%5C+cell%5C+which%5C+goes%5C+meiosis%5C+to%5C+form%5C+a%5C+linear%5C+tetrad.%5C+The%5C+chalazal%5C+megaspore%5C+of%5C+the%5C+tetrad%5C+is%5C+functional.%5C+The%5C+development%5C+of%5C+embryo%5C+sac%5C+conforms%5C+to%5C+the%5C+polygonum%5C+type.%5C+There%5C+are%5C+six%5C+ovules%5C+in%5C+the%5C+ovary%5C+of%5C+T.%5C+doichangensis%2C%5C+and%5C+only%5C+one%5C+develops%5C+into%5C+a%5C+seed%5C+in%5C+normal%5C+fruits.%5C+In%5C+the%5C+process%5C+of%5C+megasporogenesis%5C+and%5C+development%5C+of%5C+female%5C+gametophyte%2C%5C+there%5C+are%5C+several%5C+links%5C+of%5C+abortion%2C%5C+and%5C+93.3%25%5C+of%5C+mature%5C+embryo%5C+sacs%5C+is%5C+aborted.2.%5C+Morphological%5C+characters%5C+and%5C+germination%5C+of%5C+seeds%EF%BC%8CMost%5C+of%5C+the%5C+variation%5C+occurred%5C+among%5C+individual%5C+trees%5C+within%5C+populations%5C+in%5C+seed%5C+morphological%5C+traits%5C+%5C%28length%2C%5C+width%5C+and%5C+1000%5C-seed%5C+weight%5C%29%5C+and%5C+germination%5C-related%5C+indices%5C+%5C%28germination%5C+percentage%2C%5C+germination%5C+index%5C+and%5C+vigor%5C+index%5C%29.%5C+In%5C+addition%2C%5C+the%5C+variation%5C+in%5C+percentage%5C+of%5C+well%5C-developed%5C+seeds%5C+among%5C+populations%5C+and%5C+among%5C+individual%5C+trees%5C+within%5C+populations%5C+is%5C+equal%2C%5C+each%5C+accounting%5C+for%5C+48%25.%5C+Each%5C+of%5C+seed%5C+morphological%5C+traits%5C+has%5C+significantly%5C+positive%5C+correlation%5C+with%5C+each%5C+other%5C+%5C%28p%5C+%3C%5C+0.01%5C%29%2C%5C+but%5C+they%5C+have%5C+no%5C+significant%5C+correlation%5C+with%5C+percentage%5C+of%5C+well%5C-developed%5C+seeds%5C+and%5C+germination%5C-related%5C+indices.%5C+In%5C+the%5C+same%5C+batch%5C+of%5C+seeds%5C+of%5C+T.%5C+doichangensis%2C%5C+there%5C+are%5C+light%5C-colored%5C+and%5C+dark%5C-colored%5C+seed%5C+coats%2C%5C+and%5C+development%5C+of%5C+light%5C-colored%5C+seeds%5C+is%5C+significantly%5C+poorer%5C+than%5C+that%5C+of%5C+dark%5C-colored%5C+seeds.The%5C+sensitivity%5C+of%5C+seeds%5C+to%5C+high%5C+temperature%5C+varys%5C+in%5C+different%5C+stages%5C+of%5C+seed%5C+imbibition.%5C+In%5C+each%5C+stage%2C%5C+heat%5C+acclimatization%5C+don%E2%80%99t%5C+increase%5C+germination%5C+percentage%2C%5C+germination%5C+index%5C+and%5C+fresh%5C+weight%5C+of%5C+seedlings.%5C+If%5C+the%5C+distilled%5C+water%5C+is%5C+substituted%5C+by%5C+solution%5C+of%5C+SA%5C+during%5C+seed%5C+imbibition%2C%5C+seed%5C+germination%5C+and%5C+germination%5C+index%5C+after%5C+heat%5C+shock%5C+are%5C+not%5C+significantly%5C+different%5C+from%5C+control%2C%5C+but%5C+they%5C+are%5C+significantly%5C+higher%5C+than%5C+that%5C+of%5C+other%5C+treatments.%5C+Moreover%2C%5C+when%5C+the%5C+seeds%5C+are%5C+treatmented%5C+with%5C+SA%2C%5C+the%5C+fresh%5C+weight%5C+of%5C+seedlings%5C+is%5C+significantly%5C+higher%5C+than%5C+that%5C+of%5C+control%5C+and%5C+other%5C+treatments.3.%5C+Seed%5C+conservation%EF%BC%8CSeeds%5C+of%5C+T.%5C+doichangensis%5C+belong%5C+to%5C+orthodox%5C+seeds%5C+which%5C+can%5C+tolerate%5C+certain%5C+level%5C+of%5C+dehydration.%5C+The%5C+condition%5C+of%5C+low%5C+temperature%5C+and%5C+low%5C+water%5C+content%5C+of%5C+seeds%5C+is%5C+conducive%5C+to%5C+seed%5C+conservation.Germination%5C+of%5C+fresh%5C+seeds%5C+shows%5C+significant%5C+variation%5C+among%5C+populations%2C%5C+howerer%2C%5C+germination%5C+of%5C+the%5C+seeds%5C+after%5C+storage%5C+for%5C+one%5C+year%5C+in%5C+room%5C+temperatu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Data Analysisin Vegetation Ecology
期刊论文
出版物, 3111, 期号: 0, 页码: 1-297
作者:
Otto Wildi
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浏览/下载：142/2
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提交时间：2017/07/24
Ectomycorrhizal synthesis between two Tuber species and six tree species: are different host-fungus combinations having dissimilar impacts on host plant growth?
期刊论文
MYCORRHIZA, 2022, 卷号: 32, 期号: 3-4, 页码: 341-351
作者:
Huang, Lan-Lan
;
Wang, Yan-Liang
;
Guerin-Laguette, Alexis
;
Wang, Ran
;
Zhang, Peng
;
Li, Yong-Mei
;
Yu, Fu-Qiang
Adobe PDF(1425Kb)
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浏览/下载：59/2
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提交时间：2024/04/30
Ascomycetes
Tuber formosanum
T. pseudohimalayense
Broad-leaved tree
Pinus armandii
Truffle cultivation
LACTARIUS-DELICIOSUS
NEW-ZEALAND
MYCORRHIZAL
TRUFFLES
SOIL
ASSOCIATIONS
CULTIVATION
FORMOSANUM
EFFICIENCY
SEEDLINGS
Plastid phylogenomic analyses of Fagales reveal signatures of conflict and ancient chloroplast capture
期刊论文
MOLECULAR PHYLOGENETICS AND EVOLUTION, 2021, 卷号: 163, 页码: 107232
作者:
Yang,Ying-Ying
;
Qu,Xiao-Jian
;
Zhang,Rong
;
Stull,Gregory W.
;
Yi,Ting-Shuang
Adobe PDF(2469Kb)
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浏览/下载：89/15
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提交时间：2022/04/02
Betulaceae
Juglandaceae
Myricaceae
Quercus
Phylogenetics
Chloroplast capture
RESTRICTION SITE VARIATION
INTERSPECIFIC GENE FLOW
DNA-SEQUENCES
EVOLUTIONARY HISTORY
MOLECULAR PHYLOGENY
CLADISTIC-ANALYSIS
SEED PLANTS
NUCLEAR
BETULACEAE
DIVERSIFICATION
Composition of woody plant communities drives macrofungal community composition in three climatic regions
期刊论文
JOURNAL OF VEGETATION SCIENCE, 2021, 卷号: 32, 期号: 2, 页码: e13001
作者:
Li,Huili
;
Guo,Jiayu
;
Ye,Lei
;
Gui,Heng
;
Hyde,Kevin David
;
Xu,Jianchu
;
Mortimer,Peter Edward
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Adobe PDF(1613Kb)
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浏览/下载：120/14
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提交时间：2022/04/02
alpha diversity
beta diversity
climatic factors
community congruence
ecological distribution pattern
epigeous macrofungi
SPECIES RICHNESS
FUNGAL DIVERSITY
VASCULAR PLANTS
ECTOMYCORRHIZAL FUNGI
SITKA SPRUCE
FOREST
BIODIVERSITY
ABUNDANCE
MUSHROOMS
PATTERNS
Elevation-specific responses of phenology in evergreen oaks from their low-dry to their extreme high-cold range limits in the SE Himalaya
期刊论文
ALPINE BOTANY, 2021, 卷号: 131, 期号: 1, 页码: 89-102
作者:
Wang,Song-Wei
;
He,Xiao-Fang
;
Chen,Jian-Guo
;
Sun,Hang
;
Koerner,Christian
;
Yang,Yang
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|
Adobe PDF(3532Kb)
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浏览/下载：83/8
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提交时间：2022/04/02
Drought
Low temperature
Leaf traits
Growth
Mountain
Niche boundary
Quercus
BUD-BURST
LOW-TEMPERATURE
TREE PHENOLOGY
LEAF PHENOLOGY
SPRING FROST
SESSILE OAK
GROWTH
QUERCUS
POPULATIONS
DROUGHT
Higher Elevations Tend to Have Higher Proportion of Plant Species With Glandular Trichomes
期刊论文
FRONTIERS IN PLANT SCIENCE, 2021, 卷号: 12, 页码: 632464
作者:
Wu,Rui
;
Lev-Yadun,Simcha
;
Sun,Lu
;
Sun,Hang
;
Song,Bo
Adobe PDF(4500Kb)
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浏览/下载：73/26
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提交时间：2022/04/02
biotic interaction
elevation
glandular trichome
growth form
herbivorous insect
water availability
temperature
HIRSUTUM F GLABRATUM
LATITUDINAL VARIATION
RESOURCE AVAILABILITY
CONDENSED TANNINS
GROWTH FORM
HERBIVORY
RESISTANCE
RICHNESS
PATTERNS
TRAITS
Water relations of trailing-edge evergreen oaks in the semi-arid upper Yangtze region, SE Himalaya
期刊论文
JOURNAL OF SYSTEMATICS AND EVOLUTION, 2021, 卷号: 59, 期号: 6, 页码: 1256-1265
作者:
He,Xiao-Fang
;
Wang,Song-Wei
;
Sun,Hang
;
Koerner,Christian
;
Yang,Yang
Adobe PDF(917Kb)
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浏览/下载：105/45
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提交时间：2022/04/02
adaptation
Himalaya
monsoon climate
Quercus
species distribution
water stress
CARBON ISOTOPE DISCRIMINATION
SOUTHERN RANGE-EDGE
QUERCUS-ROBUR
GROWTH DECLINE
USE EFFICIENCY
FOREST TREES
RESPONSES
DROUGHT
PHOTOSYNTHESIS
ILEX
基于转录组数据的蔷薇类和天南星科系统发育基因组学研究
学位论文
, 2020
作者:
赵磊
Adobe PDF(7010Kb)
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浏览/下载：36/0
|
提交时间：2023/11/02
金沙江干热河谷长穗高山栎适应策略及其生态恢复应用初探
学位论文
, 2020
作者:
何小芳
Adobe PDF(2872Kb)
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浏览/下载：20/1
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提交时间：2023/11/02
Refined families of Dothideomycetes: Dothideomycetidae and Pleosporomycetidae
期刊论文
MYCOSPHERE, 2020
作者:
Hongsanan, S.
;
Hyde, K. D.
;
Phookamsak, R.
;
Wanasinghe, D. N.
;
McKenzie, E. H. C.
;
Sarma, V. V.
;
Boonmee, S.
;
Luecking, R.
;
Bhat, D. J.
;
Liu, N. G.
;
Tennakoon, D. S.
;
Pem, D. S.
;
Karunarathna, A.
;
Jiang, S. H.
;
Jones, E. B. G.
;
Phillips, A. J. L.
;
Manawasinghe, I. S.
;
Tibpromma, S.
;
Jayasiri, S. C.
;
Sandamali, D. S.
;
Jayawardena, R. S.
;
Wijayawardene, N. N.
;
Ekanayaka, A. H.
;
Jeewon, R.
;
Lu, Y. Z.
;
Dissanayake, A. J.
;
Zeng, X. Y.
;
Luo, Z. L.
;
Tian, Q.
;
Phukhamsakda, C.
;
Thambugala, K. M.
;
Dai, D. Q.
;
Chethana, K. W. T.
;
Samarakoon, M. C.
;
Ertz, D.
;
Bao, D. F.
;
Doilom, M.
;
Liu, J. K.
;
Perez-Ortega, S.
;
Suija, A.
;
Senwanna, C.
;
Wijesinghe, S. N.
;
Konta, S.
;
Niranjan, M.
;
Zhang, S. N.
;
Ariyawansa, H. A.
;
Jiang, H. B.
;
Zhang, J. F.
;
Norphanphoun, C.
;
de Silva, N., I
;
Thiyagaraja, V
;
Zhang, H.
;
Bezerra, J. D. P.
;
Miranda-Gonzalez, R.
;
Aptroot, A.
;
Kashiwadani, H.
;
Harishchandra, D.
;
Serusiaux, E.
;
Aluthmuhandiram, J. V. S.
;
Abeywickrama, P. D.
;
Devadatha, B.
;
Wu, H. X.
;
Moon, K. H.
;
Gueidan, C.
;
Schumm, F.
;
Bundhun, D.
;
Mapook, A.
;
Monkai, J.
;
Chomnunti, P.
;
Suetrong, S.
;
Chaiwan, N.
;
Dayarathne, M. C.
;
Yang, J.
;
Rathnayaka, A. R.
;
Bhunjun, C. S.
;
Xu, J. C.
;
Zheng, J. S.
;
Liu, G. L.
;
Feng, Y.
;
Xie, N.
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提交时间：2021/01/05
