The relationship between atmospheric particulate matter, leaf surface microstructure, and the phyllosphere microbial diversity of Ulmus L.
Atmospheric pollution
Elm
Foliar microstructures
PM-borne microorganisms
Phyllosphere microbiome
Journal
BMC plant biology
ISSN: 1471-2229
Titre abrégé: BMC Plant Biol
Pays: England
ID NLM: 100967807
Informations de publication
Date de publication:
17 Jun 2024
17 Jun 2024
Historique:
received:
03
03
2024
accepted:
31
05
2024
medline:
17
6
2024
pubmed:
17
6
2024
entrez:
16
6
2024
Statut:
epublish
Résumé
Plants can retain atmospheric particulate matter (PM) through their unique foliar microstructures, which has a profound impact on the phyllosphere microbial communities. Yet, the underlying mechanisms linking atmospheric particulate matter (PM) retention by foliar microstructures to variations in the phyllosphere microbial communities remain a mystery. In this study, we conducted a field experiment with ten Ulmus lines. A series of analytical techniques, including scanning electron microscopy, atomic force microscopy, and high-throughput amplicon sequencing, were applied to examine the relationship between foliar surface microstructures, PM retention, and phyllosphere microbial diversity of Ulmus L. We characterized the leaf microstructures across the ten Ulmus lines. Chun exhibited a highly undulated abaxial surface and dense stomatal distribution. Langya and Xingshan possessed dense abaxial trichomes, while Lieye, Zuiweng, and Daguo had sparsely distributed, short abaxial trichomes. Duomai, Qingyun, and Lang were characterized by sparse stomata and flat abaxial surfaces, whereas Jinye had sparsely distributed but extensive stomata. The mean leaf retention values for total suspended particulate (TSP), PM Based on our findings, a three-factor network profile was constructed, which provides a foundation for further exploration into how different plants retain PM through foliar microstructures, thereby impacting phyllosphere microbial communities.
Sections du résumé
BACKGROUND
BACKGROUND
Plants can retain atmospheric particulate matter (PM) through their unique foliar microstructures, which has a profound impact on the phyllosphere microbial communities. Yet, the underlying mechanisms linking atmospheric particulate matter (PM) retention by foliar microstructures to variations in the phyllosphere microbial communities remain a mystery. In this study, we conducted a field experiment with ten Ulmus lines. A series of analytical techniques, including scanning electron microscopy, atomic force microscopy, and high-throughput amplicon sequencing, were applied to examine the relationship between foliar surface microstructures, PM retention, and phyllosphere microbial diversity of Ulmus L.
RESULTS
RESULTS
We characterized the leaf microstructures across the ten Ulmus lines. Chun exhibited a highly undulated abaxial surface and dense stomatal distribution. Langya and Xingshan possessed dense abaxial trichomes, while Lieye, Zuiweng, and Daguo had sparsely distributed, short abaxial trichomes. Duomai, Qingyun, and Lang were characterized by sparse stomata and flat abaxial surfaces, whereas Jinye had sparsely distributed but extensive stomata. The mean leaf retention values for total suspended particulate (TSP), PM
CONCLUSIONS
CONCLUSIONS
Based on our findings, a three-factor network profile was constructed, which provides a foundation for further exploration into how different plants retain PM through foliar microstructures, thereby impacting phyllosphere microbial communities.
Identifiants
pubmed: 38880875
doi: 10.1186/s12870-024-05232-z
pii: 10.1186/s12870-024-05232-z
doi:
Substances chimiques
Particulate Matter
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
566Subventions
Organisme : Science and Technology Development Fund of Central Guidance on Local, China
ID : 216Z6301G
Organisme : Science and Technology Development Fund of Central Guidance on Local, China
ID : 216Z6301G
Organisme : Science and Technology Development Fund of Central Guidance on Local, China
ID : 216Z6301G
Organisme : Science and Technology Development Fund of Central Guidance on Local, China
ID : 216Z6301G
Organisme : Science and Technology Development Fund of Central Guidance on Local, China
ID : 216Z6301G
Organisme : Science and Technology Development Fund of Central Guidance on Local, China
ID : 216Z6301G
Organisme : Science and Technology Development Fund of Central Guidance on Local, China
ID : 216Z6301G
Organisme : Science and Technology Development Fund of Central Guidance on Local, China
ID : 216Z6301G
Organisme : Science and Technology Development Fund of Central Guidance on Local, China
ID : 216Z6301G
Organisme : Key Research and Development Program of Hebei Province, China
ID : 21326301D
Organisme : Key Research and Development Program of Hebei Province, China
ID : 21326301D
Organisme : Key Research and Development Program of Hebei Province, China
ID : 21326301D
Organisme : Key Research and Development Program of Hebei Province, China
ID : 21326301D
Organisme : Key Research and Development Program of Hebei Province, China
ID : 21326301D
Organisme : Key Research and Development Program of Hebei Province, China
ID : 21326301D
Organisme : Key Research and Development Program of Hebei Province, China
ID : 21326301D
Organisme : Key Research and Development Program of Hebei Province, China
ID : 21326301D
Organisme : Key Research and Development Program of Hebei Province, China
ID : 21326301D
Informations de copyright
© 2024. The Author(s).
Références
Meng G, Guo Z, Li J. The dynamic linkage among urbanisation, industrialisation and carbon emissions in China: insights from spatiotemporal effect. Sci Total Environ. 2021;760:144042. https://doi.org/10.1016/j.scitotenv.2020.144042 .
doi: 10.1016/j.scitotenv.2020.144042
pubmed: 33341621
Huang R, Zhang Y, Bozzetti C, Ho K, Cao J, Han Y, et al. High secondary aerosol contribution to particulate pollution during haze events in China. Nature. 2014;514(7521):218–22. https://doi.org/10.1038/nature13774 .
doi: 10.1038/nature13774
pubmed: 25231863
Hu D, Jiang J. A study of smog issues and PM
doi: 10.4236/jep.2013.47086
Chi NNH, Oanh NTK. Photochemical smog modeling of PM
doi: 10.1016/j.eti.2020.101241
Wang Q, Feng J, Huang Y, Wang P, Xie M, Wan Y, et al. Dust retention capability and leaf surface micromorphology of 15 broad-leaved tree species in Wuhan. Acta Ecol Sin. 2020;40(1):213–22. https://doi.org/10.5846/stxb201808241808 .
doi: 10.5846/stxb201808241808
Tan X, Liu L, Wu D. Relationship between leaf dust retention capacity and leaf microstructure of six common tree species for campus greening. Int J Phytoremediat. 2022;1–9. https://doi.org/10.1080/15226514.2021.2024135 .
Corada K, Woodward H, Alaraj H, Collins CM, de Nazelle A. A systematic review of the leaf traits considered to contribute to removal of airborne particulate matter pollution in urban areas. Environ Pollut. 2021;269:116104. https://doi.org/10.1016/j.envpol.2020.116104 .
doi: 10.1016/j.envpol.2020.116104
pubmed: 33339707
Łukowski A, Popek R, Karolewski P. Particulate matter on foliage of Betula pendula, Quercus robur, and Tilia cordata: deposition and ecophysiology. Environ Sci Pollut Res. 2020;27:10296–307. https://doi.org/10.1007/s11356-020-07672-0 .
doi: 10.1007/s11356-020-07672-0
Deng L, Qian J, Liao R, Tong H. Pollution characteristics of atmospheric particulates in Chengdu from August to September in 2009 and their relationship with meteorological conditions. China Environ Sci. 2012;32(8):1433–8.
Vorholt JA. Microbial life in the phyllosphere. Nat Rev Microbiol. 2012;10(12):828–40. https://doi.org/10.1038/nrmicro2910 .
doi: 10.1038/nrmicro2910
pubmed: 23154261
De Mandal S, Jeon J. Phyllosphere Microbiome in Plant Health and Disease. Plants. 2023;12(19):3481. https://doi.org/10.3390/plants12193481 .
doi: 10.3390/plants12193481
pubmed: 37836221
pmcid: 10575124
Mandal M, Das S, Roy A, Rakwal R, Jones OA, Popek R, et al. Interactive relations between plants, phyllosphere microbial community, and particulate matter pollution. Sci Total Environ. 2023;164352. https://doi.org/10.1016/j.scitotenv.2023.164352 .
Andrews JH, Harris RF. The ecology and biogeography of microorganisms on plant surfaces. Annu Rev Phytopathol. 2000;38(1):145–80. https://doi.org/10.1146/annurev.phyto.38.1.145 .
doi: 10.1146/annurev.phyto.38.1.145
pubmed: 11701840
Bashir I, War AF, Rafiq I, Reshi ZA, Rashid I, Shouche YS. Phyllosphere microbiome: diversity and functions. Microbiol Res. 2022;254:126888. https://doi.org/10.1016/j.micres.2021.126888 .
doi: 10.1016/j.micres.2021.126888
pubmed: 34700185
Morris C. Phyllosphere. Encycl Life Sci. 2002. https://doi.org/10.1038/npg.els.0000400Citat .
doi: 10.1038/npg.els.0000400Citat
Osono T. Diversity and ecology of endophytic and epiphytic fungi of tree leaves in Japan: a review. Adv Endophyt Res. 2013;3–26. https://doi.org/10.1007/978-81-322-1575-2_1 .
Bulgarelli D, Schlaeppi K, Spaepen S, Van Themaat EVL, Schulze-Lefert P. Structure and functions of the bacterial microbiota of plants. Annu Rev Plant Biol. 2013;64:807–38. https://doi.org/10.1146/annurev-arplant-050312-120106 .
doi: 10.1146/annurev-arplant-050312-120106
pubmed: 23373698
Espenshade J, Thijs S, Gawronski S, Bové H, Weyens N, Vangronsveld J. Influence of urbanization on epiphytic bacterial communities of the platanus× hispanica tree leaves in a biennial study. Front Microbiol. 2019;10:675. https://doi.org/10.3389/fmicb.2019.00675 .
doi: 10.3389/fmicb.2019.00675
pubmed: 31024477
pmcid: 6460055
Pollegioni P, Mattioni C, Ristorini M, Occhiuto D, Canepari S, Korneykova MV, et al. Diversity and source of airborne microbial communities at differential polluted sites of Rome. Atmos. 2022;13(2):224. https://doi.org/10.3390/atmos13020224 .
doi: 10.3390/atmos13020224
Wu Z, Raven PH, Hong D. Flora of China. Volume 5. Ulmaceae through Basellaceae. Science; 2003.
Chen P, Liu P, Zhang Q, Bu C, Lu C, Srivastava S, et al. Gene coexpression network analysis indicates that hub genes related to photosynthesis and starch synthesis modulate salt stress tolerance in Ulmus pumila. Int J Mol Sci. 2021;22(9):4410. https://doi.org/10.3390/ijms22094410 .
doi: 10.3390/ijms22094410
pubmed: 33922506
pmcid: 8122946
Mikolajewski D, D’Amico IIIV, Sonti NF, Pinchot CC, Flower CE, Roman LA, et al. Restoring the iconic Ulmus americana to urban landscapes: early tree growth responds to aboveground conditions. Urban Urban Green. 2022;74:127675. https://doi.org/10.1016/j.ufug.2022.127675 .
doi: 10.1016/j.ufug.2022.127675
Yan S, Huang Y, Zhang J, Liu Y, Yang H. A new Ulmus pumila Cultivar‘Yangguang Nühai’. Acta Hortic Sin. 2015;42(5):1017–8. https://doi.org/10.16420/j.issn.0513-353x.2014-0491 .
doi: 10.16420/j.issn.0513-353x.2014-0491
Zuo L, Zhang S, Liu Y, Huang Y, Yang M, Wang J. The reason for growth inhibition of Ulmus pumila ‘Jinye’: lower resistance and abnormal development of chloroplasts slow down the accumulation of energy. Int J Mol Sci. 2019;20(17):4227. https://doi.org/10.3390/ijms20174227 .
doi: 10.3390/ijms20174227
pubmed: 31470529
pmcid: 6747506
Song B, Zhang H, Jiao L, Jing Z, Li H, Wu S. Effect of high-level fine particulate matter and its interaction with meteorological factors on AECOPD in Shijiazhuang, China. Sci Rep. 2022;12(1):1–9. https://doi.org/10.1038/s41598-022-12791-4 .
doi: 10.1038/s41598-022-12791-4
Ministry of Environmental Protection of China. Ambient Air Quality Standards (GB 3095 – 2012). 2012. https://www.mee.gov.cn/ywgz/fgbz/bz/bzwb/dqhjbh/dqhjzlbz/201203/t20120302_224165.shtml .
Guo M, Wu F, Hao G, Qi Q, Li R, Li N, et al. Bacillus subtilis improves immunity and disease resistance in rabbits. Front Immunol. 2017;8:354. https://doi.org/10.3389/fimmu.2017.00354 .
doi: 10.3389/fimmu.2017.00354
pubmed: 28424690
pmcid: 5372816
Scibetta S, Schena L, Abdelfattah A, Pangallo S, Cacciola SO. Selection and experimental evaluation of universal primers to study the fungal microbiome of higher plants. Phytobiomes J. 2018;2(4):225–36. https://doi.org/10.1094/PBIOMES-02-18-0009-R .
doi: 10.1094/PBIOMES-02-18-0009-R
Chen S, Zhou Y, Chen Y, Gu J. Fastp: an ultra-fast all-in-one FASTQ preprocessor. Bioinformatics. 2018;34(17):i884–90. https://doi.org/10.1093/bioinformatics/bty560 .
doi: 10.1093/bioinformatics/bty560
pubmed: 30423086
pmcid: 6129281
Magoč T, Salzberg SL. FLASH: fast length adjustment of short reads to improve genome assemblies. Bioinformatics. 2011;27(21):2957–63. https://doi.org/10.1093/bioinformatics/btr507 .
doi: 10.1093/bioinformatics/btr507
pubmed: 21903629
pmcid: 3198573
Bokulich NA, Subramanian S, Faith JJ, Gevers D, Gordon JI, Knight R, et al. Quality-filtering vastly improves diversity estimates from Illumina amplicon sequencing. Nat Methods. 2013;10(1):57–9. https://doi.org/10.1038/nmeth.2276 .
doi: 10.1038/nmeth.2276
pubmed: 23202435
Chiarello M, McCauley M, Villéger S, Jackson CR. Ranking the biases: the choice of OTUs vs. ASVs in 16S rRNA amplicon data analysis has stronger effects on diversity measures than rarefaction and OTU identity threshold. PLoS ONE. 2022;17(2):e0264443. https://doi.org/10.1371/journal.pone.0264443 .
doi: 10.1371/journal.pone.0264443
pubmed: 35202411
pmcid: 8870492
Edgar RC. Search and clustering orders of magnitude faster than BLAST. Bioinformatics. 2010;26(19):2460–1. https://doi.org/10.1093/bioinformatics/btq461 .
doi: 10.1093/bioinformatics/btq461
pubmed: 20709691
Nilsson RH, Larsson K-H, Taylor AFS, Bengtsson-Palme J, Jeppesen TS, Schigel D, et al. The UNITE database for molecular identification of fungi: handling dark taxa and parallel taxonomic classifications. Nucleic Acids Res. 2019;47(D1):D259–64. https://doi.org/10.1093/nar/gky1022 .
doi: 10.1093/nar/gky1022
pubmed: 30371820
Caporaso JG, Kuczynski J, Stombaugh J, Bittinger K, Bushman FD, Costello EK, et al. QIIME allows analysis of high-throughput community sequencing data. Nat Methods. 2010;7(5):335–6. https://doi.org/10.1038/nmeth.f.303 .
doi: 10.1038/nmeth.f.303
pubmed: 20383131
pmcid: 3156573
Oksanen J. vegan: Community Ecology Package-R package version 1.17-8. http://CRAN R-project org/package = vegan. 2011.
Douglas GM, Maffei VJ, Zaneveld J, Yurgel SN, Brown JR, Taylor CM, et al. PICRUSt2: an improved and extensible approach for metagenome inference. BioRxiv. 2019;672295. https://doi.org/10.1101/672295 .
Nguyen NH, Song Z, Bates ST, Branco S, Tedersoo L, Menke J, et al. FUNGuild: an open annotation tool for parsing fungal community datasets by ecological guild. Fungal Ecol. 2016;20:241–8. https://doi.org/10.1016/j.funeco.2015.06.006 .
doi: 10.1016/j.funeco.2015.06.006
Rokhbakhsh-Zamin F, Sachdev D, Kazemi-Pour N, Engineer A, Pardesi KR, Zinjarde S, et al. Characterization of plant-growth-promoting traits of Acinetobacter species isolated from rhizosphere of Pennisetum glaucum. J Microbiol Biotechnol. 2011;21(6):556–66. https://doi.org/10.4014/jmb.1012.12006 .
doi: 10.4014/jmb.1012.12006
pubmed: 21715961
Preston GM. Plant perceptions of plant growth-promoting Pseudomonas. Philos Trans R Soc Lond B Biol Sci. 2004;359(1446):907–18. https://doi.org/10.1098/rstb.2003.1384 .
doi: 10.1098/rstb.2003.1384
pubmed: 15306406
pmcid: 1693381
Jha CK, Aeron A, Patel BV, Maheshwari DK, Saraf M. Enterobacter: role in plant growth promotion. Bact Agrobiol Plant Growth Responses. 2011:159–82. https://doi.org/10.1007/978-3-642-20332-9_8 .
De Vleesschauwer D, Höfte M. Using Serratia plymuthica to control fungal pathogens of plants. CAB Reviews. 2003;2(046). https://doi.org/10.1079/PAVSNNR20072046 .
Smullen J, Koutsou G, Foster H, Zumbé A, Storey D. The antibacterial activity of plant extracts containing polyphenols against Streptococcus mutans. Caries Res. 2007;41(5):342–9. https://doi.org/10.1159/000104791 .
doi: 10.1159/000104791
pubmed: 17713333
De Gusseme B, Vanhaecke L, Verstraete W, Boon N. Degradation of acetaminophen by Delftia tsuruhatensis and Pseudomonas aeruginosa in a membrane bioreactor. Water Res. 2011;45(4):1829–37. https://doi.org/10.1016/j.watres.2010.11.040 .
doi: 10.1016/j.watres.2010.11.040
pubmed: 21167545
Ryan RP, Monchy S, Cardinale M, Taghavi S, Crossman L, Avison MB, et al. The versatility and adaptation of bacteria from the genus Stenotrophomonas. Nat Rev Microbiol. 2009;7(7):514–25. https://doi.org/10.1038/nrmicro2163 .
doi: 10.1038/nrmicro2163
pubmed: 19528958
Al-Quwaie DA. The role of Streptomyces species in controlling plant diseases: a comprehensive review. Australas Plant Pathol. 2024;53(1):1–14. https://doi.org/10.1007/s13313-023-00959-z .
doi: 10.1007/s13313-023-00959-z
Walterson AM, Stavrinides J. Pantoea: insights into a highly versatile and diverse genus within the Enterobacteriaceae. FEMS Microbiol Rev. 2015;39(6):968–84. https://doi.org/10.1093/femsre/fuv027 .
doi: 10.1093/femsre/fuv027
pubmed: 26109597
Chhetri G, Kim I, Kang M, So Y, Kim J, Seo T. An isolated Arthrobacter sp. enhances rice (Oryza sativa L.) plant growth. Microorganisms. 2022;10(6):1187. https://doi.org/10.3390/microorganisms10061187 .
doi: 10.3390/microorganisms10061187
pubmed: 35744704
pmcid: 9228311
Wang Z, Luo W, Cheng S, Zhang H, Zong J, Zhang Z. Ralstonia solanacearum–a soil borne hidden enemy of plants: research development in management strategies, their action mechanism and challenges. Front Plant Sci. 2023;14:1141902. https://doi.org/10.3389/fpls.2023.1141902 .
doi: 10.3389/fpls.2023.1141902
pubmed: 36909396
pmcid: 9998985
Naher UA, Othman R, Shamsuddin ZH, Saud HM, Ismail MR. Growth enhancement and root colonization of rice seedlings by Rhizobium and Corynebacterium spp. Int J Agric Biol. 2009;11:586–90.
Răut I, Călin M, Capră L, Gurban A-M, Doni M, Radu N, et al. Cladosporium sp. isolate as fungal plant growth promoting agent. Agron. 2021;11(2):392. https://doi.org/10.3390/agronomy11020392 .
doi: 10.3390/agronomy11020392
Mauricio-Castillo JA, Salas-Muñoz S, Reveles-Torres LR, Salas-Luevano MA, Salazar-Badillo FB. Could Alternaria solani IA300 be a plant growth-promoting fungus? Eur J Plant Pathol. 2020;157:413–9. https://doi.org/10.1007/s10658-020-01984-0 .
doi: 10.1007/s10658-020-01984-0
Hung R, Rutgers SL. Applications of aspergillus in plant growth promotion. New and future developments in microbial biotechnology and bioengineering. Elsevier; 2016. pp. 223–7. https://doi.org/10.1016/B978-0-444-63505-1.00018-X .
Silambarasan S, Vangnai AS. Plant-growth promoting Candida sp. AVGB4 with capability of 4-nitroaniline biodegradation under drought stress. Ecotoxicol Environ Saf. 2017;139:472–80. https://doi.org/10.1016/j.ecoenv.2017.02.018 .
doi: 10.1016/j.ecoenv.2017.02.018
pubmed: 28214644
Radhakrishnan R, Kang S-M, Baek I-Y, Lee I-J. Characterization of plant growth-promoting traits of Penicillium species against the effects of high soil salinity and root disease. J Plant Interact. 2014;9(1):754–62. https://doi.org/10.1080/17429145.2014.930524 .
doi: 10.1080/17429145.2014.930524
Takamatsu S, Ito H, Shiroya Y, Kiss L, Heluta V. First comprehensive phylogenetic analysis of the genus Erysiphe (Erysiphales, Erysiphaceae) I. The Microsphaera lineage. Mycol. 2015;107(3):475–89. https://doi.org/10.3852/15-007 .
doi: 10.3852/15-007
Summerell B, Burgess L, Backhouse D, Bullock S, Swan L. Natural occurrence of perithecia of Gibberella coronicola on wheat plants with crown rot in Australia. Australas Plant Pathol. 2001;30:353–6. https://doi.org/10.1071/AP01045 .
doi: 10.1071/AP01045
Vollmeister E, Schipper K, Baumann S, Haag C, Pohlmann T, Stock J, et al. Fungal development of the plant pathogen Ustilago maydis. FEMS Microbiol Rev. 2012;36(1):59–77. https://doi.org/10.1111/j.1574-6976.2011.00296.x .
doi: 10.1111/j.1574-6976.2011.00296.x
pubmed: 21729109
Arie T. Fusarium diseases of cultivated plants, control, diagnosis, and molecular and genetic studies. J Pestic Sci. 2019;44(4):275–81. https://doi.org/10.1584/jpestics.J19-03 .
doi: 10.1584/jpestics.J19-03
pubmed: 31777447
pmcid: 6861427
De Silva DD, Crous PW, Ades PK, Hyde KD, Taylor PW. Life styles of Colletotrichum species and implications for plant biosecurity. Fungal Biol Rev. 2017;31(3):155–68. https://doi.org/10.1016/j.fbr.2017.05.001 .
doi: 10.1016/j.fbr.2017.05.001
Khan SA, Hamayun M, Yoon H, Kim H-Y, Suh S-J, Hwang S-K, et al. Plant growth promotion and Penicillium Citrinum. BMC Microbiol. 2008;8:1–10.
doi: 10.1186/1471-2180-8-231
Guo X, Reddy GV, He J, Li J, Shi P. Mean-variance relationships of leaf bilateral asymmetry for 35 species of plants and their implications. Glob Ecol Conserv. 2020;23:e01152. https://doi.org/10.1016/j.gecco.2020.e01152 .
doi: 10.1016/j.gecco.2020.e01152
De Lopez U, Duro-García MJ, Soto A. Leaf morphology of progenies in Q. Suber, Q. ilex, and their hybrids using multivariate and geometric morphometric analysis. iForest-Biogeosci for. 2018;11(1):90. https://doi.org/10.3832/ifor2577-010 .
doi: 10.3832/ifor2577-010
Yang K, Wu J, Li X, Pang X, Yuan Y, Qi G, et al. Intraspecific leaf morphological variation in Quercus dentata Thunb.: a comparison of traditional and geometric morphometric methods, a pilot study. J Res. 2022;33(6):1751–64. https://doi.org/10.1007/s11676-022-01452-x .
doi: 10.1007/s11676-022-01452-x
Yang Q, Yang X, Wang L, Zheng B, Cai Y, Ogutu CO, et al. Two R2R3-MYB genes cooperatively control trichome development and cuticular wax biosynthesis in Prunus persica. New Phytol. 2022;234(1):179–96. https://doi.org/10.1111/NPH.17965 .
doi: 10.1111/NPH.17965
pubmed: 35023174
Yang S, Wang Y, Zhu H, Zhang M, Wang D, Xie K, et al. A novel HD-Zip I/C2H2‐ZFP/WD‐repeat complex regulates the size of spine base in cucumber. New Phytol. 2022;233(6):2643–58. https://doi.org/10.1111/nph.17967 .
doi: 10.1111/nph.17967
pubmed: 35037268
Gudesblat GE, Schneider-Pizoń J, Betti C, Mayerhofer J, Vanhoutte I, Van Dongen W, et al. SPEECHLESS integrates brassinosteroid and stomata signalling pathways. Nat Cell Biol. 2012;14(5):548–54. https://doi.org/10.1038/ncb2471 .
doi: 10.1038/ncb2471
pubmed: 22466366
Kanaoka MM, Pillitteri LJ, Fujii H, Yoshida Y, Bogenschutz NL, Takabayashi J, et al. SCREAM/ICE1 and SCREAM2 specify three cell-state transitional steps leading to Arabidopsis stomatal differentiation. Plant Cell. 2008;20(7):1775–85. https://doi.org/10.1105/tpc.108.060848 .
doi: 10.1105/tpc.108.060848
pubmed: 18641265
pmcid: 2518248
Zuch DT, Doyle SM, Majda M, Smith RS, Robert S, Torii KU. Cell biology of the leaf epidermis: fate specification, morphogenesis, and coordination. Plant Cell. 2022;34(1):209–27. https://doi.org/10.1093/plcell/koab250 .
doi: 10.1093/plcell/koab250
pubmed: 34623438
Shao F, Wang L, Sun F, Li G, Yu L, Wang Y, et al. Study on different particulate matter retention capacities of the leaf surfaces of eight common garden plants in Hangzhou, China. Sci Total Environ. 2019;652:939–51. https://doi.org/10.1016/j.scitotenv.2018.10.182 .
doi: 10.1016/j.scitotenv.2018.10.182
pubmed: 30380499
Yue C, Cui K, Duan J, Wu X, Yan P, Rodriguez C, et al. The retention characteristics for water-soluble and water-insoluble particulate matter of five tree species along an air pollution gradient in Beijing, China. Sci Total Environ. 2021;767:145497. https://doi.org/10.1016/j.scitotenv.2021.145497 .
doi: 10.1016/j.scitotenv.2021.145497
pubmed: 33579558
Yu J, Xu L, Liu C, Li Y, Pang X, Liu Z, et al. Comparative analysis of the dust retention capacity and leaf microstructure of 11 Sophora japonica clones. PLoS ONE. 2021;16(9):e0254627. https://doi.org/10.1371/journal.pone.0254627 .
doi: 10.1371/journal.pone.0254627
pubmed: 34492027
pmcid: 8423301
Dzierżanowski K, Popek R, Gawrońska H, Sæbø A, Gawroński SW. Deposition of particulate matter of different size fractions on leaf surfaces and in waxes of urban forest species. Int J Phytoremediat. 2011;13(10):1037–46. https://doi.org/10.1080/15226514.2011.552929 .
doi: 10.1080/15226514.2011.552929
Hermann J, Tkatchenko A. Density functional model for Van Der Waals interactions: Unifying many-body atomic approaches with nonlocal functionals. Phys Rev Lett. 2020;124(14):146401. https://doi.org/10.1103/PhysRevLett.124.146401 .
doi: 10.1103/PhysRevLett.124.146401
pubmed: 32338971
Wróblewska K, Jeong BR. Effectiveness of plants and green infrastructure utilization in ambient particulate matter removal. Environ Sci Eur. 2021;33(1):110. https://doi.org/10.1186/s12302-021-00547-2 .
doi: 10.1186/s12302-021-00547-2
pubmed: 34603905
pmcid: 8475335
Park S, Lee JK, Kwak MJ, Lim YJ, Kim H, Jeong SG, et al. Relationship between leaf traits and PM-capturing capacity of major urban-greening species. Horticulturae. 2022;8(11):1046. https://doi.org/10.3390/horticulturae8111046 .
doi: 10.3390/horticulturae8111046
Xu L, Yan Q, He P, Zhen Z, Jing Y, Duan Y et al. Combined effects of different leaf traits on foliage dust-retention capacity and stability. Air Qual Atmos Health. 2022:1–12. https://doi.org/10.1007/s11869-021-01141-4 .
Lawson T, Blatt MR. Stomatal size, speed, and responsiveness impact on photosynthesis and water use efficiency. Plant Physiol. 2014;164(4):1556–70. https://doi.org/10.1104/pp.114.237107 .
doi: 10.1104/pp.114.237107
pubmed: 24578506
pmcid: 3982722
Haworth M, Marino G, Loreto F, Centritto M. Integrating stomatal physiology and morphology: evolution of stomatal control and development of future crops. Oecologia. 2021;197(4):867–83. https://doi.org/10.1007/s00442-021-04857-3 .
doi: 10.1007/s00442-021-04857-3
pubmed: 33515295
pmcid: 8591009
Yuan Z, Ye J, Lin F, Wang X, Yang T, Bi B, et al. Relationships between Phyllosphere Bacterial communities and Leaf Functional traits in a Temperate Forest. Plants. 2023;12(22):3854. https://doi.org/10.3390/plants12223854 .
doi: 10.3390/plants12223854
pubmed: 38005751
pmcid: 10674237
Li Y, Li Z, Arafat Y, Lin W. Studies on fungal communities and functional guilds shift in tea continuous cropping soils by high-throughput sequencing. Ann Microbiol. 2020;70:1–12. https://doi.org/10.1186/s13213-020-01555-y .
doi: 10.1186/s13213-020-01555-y
Hashem AH, Attia MS, Kandil EK, Fawzi MM, Abdelrahman AS, Khader MS, et al. Bioactive compounds and biomedical applications of endophytic fungi: a recent review. Microb Cell Fact. 2023;22(1):107. https://doi.org/10.1186/s12934-023-02118-x .
doi: 10.1186/s12934-023-02118-x
pubmed: 37280587
pmcid: 10243280
Jha P, Kaur T, Chhabra I, Panja A, Paul S, Kumar V, et al. Endophytic fungi: hidden treasure chest of antimicrobial metabolites interrelationship of endophytes and metabolites. Front Microbiol. 2023;14:1227830. https://doi.org/10.3389/fmicb.2023.1227830 .
doi: 10.3389/fmicb.2023.1227830
pubmed: 37497538
pmcid: 10366620
Rodriguez RJ, Henson J, Van Volkenburgh E, Hoy M, Wright L, Beckwith F, et al. Stress tolerance in plants via habitat-adapted symbiosis. ISME J. 2008;2(4):404–16. https://doi.org/10.1038/ismej.2007.106 .
doi: 10.1038/ismej.2007.106
pubmed: 18256707
Brighigna L, Gori A, Gonnelli S, Favilli F. The influence of air pollution on the phyllosphere microflora composition of Tillandsia leaves (Bromeliaceae). Rev Biol Trop. 2000;48(2–3):511–7.
pubmed: 11354959
Gostinčar C, Zajc J, Lenassi M, Plemenitaš A, De Hoog S, Al-Hatmi AM, et al. Fungi between extremotolerance and opportunistic pathogenicity on humans. Fungal Divers. 2018;93:195–213. https://doi.org/10.1007/s13225-018-0414-8 .
doi: 10.1007/s13225-018-0414-8