Plant Diversity ›› 2020, Vol. 42 ›› Issue (01): 33-43.DOI: 10.1016/j.pld.2019.10.002
• Articles • Previous Articles Next Articles
Anuj Choudhary, Antul Kumar, Nirmaljit Kaur
Received:
2019-04-25
Revised:
2019-09-02
Online:
2020-02-29
Published:
2020-02-25
Contact:
Anuj Choudhary
Anuj Choudhary, Antul Kumar, Nirmaljit Kaur
通讯作者:
Anuj Choudhary
Anuj Choudhary, Antul Kumar, Nirmaljit Kaur. ROS and oxidative burst: Roots in plant development[J]. Plant Diversity, 2020, 42(01): 33-43.
Anuj Choudhary, Antul Kumar, Nirmaljit Kaur. ROS and oxidative burst: Roots in plant development[J]. Plant Diversity, 2020, 42(01): 33-43.
Aken, O.V., Van Breusegem, F., 2015. Licensed to kill:mitochondria, chloroplasts, and cell death. Trends Plant Sci. 20, 754-766. https://doi.org/10.1016/j.tplants.2015.08.002. Arc, E., Sechet, J., Corbineau, F., Rajjou, L., Marion-Poll, A., 2013. ABA crosstalk with ethylene and nitric oxide in seed dormancy and germination. Front. Plant Sci. 4, 63. Bahin, E., Bailly, C., Sotta, B., Kranner, I., Corbineau, F., Leymarie, J., 2011. Crosstalk between reactive oxygen species and hormonal signaling pathways regulates grain dormancy in barley. Plant Cell Environ. 34, 980-993. Bailly, C., 2004. Active oxygen species and antioxidants in seed biology. Seed Sci.Res. 14, 93-107. Bailly, C., El-Maarouf-Bouteau, H., Corbineau, F., 2008. From intracellular signaling networks to cell death:the dual role of reactive oxygen species in seed physiology. C. R. Biol. 331, 806-814. Basbouss-Serhal, I., Pateyron, S., Cochet, F., Leymarie, J., Bailly, C., 2017. 5' to 3' mRNA decay contributes to the regulation of Arabidopsis seed germination by dormancy. Plant Physiol. 173, 1709-1723. Beemster, G.T.S., Veylder, L.D., Vercruysse, S., West, S., Rombaut, D., Hummelen, P.V., Galichet, A., Gruissem, W., Inzé, D., Vuylsteke, M., 2005. Genome-wide analysis of gene expression profiles associated with cell cycle transitions in growing organs of Arabidopsis. Plant Physiol. 138, 734-743. Benitez-Alfonso, Y., Cilia, M., San Roman, A., Thomas, C., Maule, A., Hearn, S., Jackson, D., 2009. Control of Arabidopsis meristem development by thioredoxin-dependent regulation of intercellular transport. Proc. Natl. Acad. Sci. 106, 3615-3620. Bhattacharjee, S., 2012. The language of Reactive oxygen species signaling in plant. J. Bot., Le 2012, 1-22. Bussell, J.D., Reichelt, M., Wiszniewski, A.A., Gershenzon, J., Smith, S.M., 2014. Peroxisomal ATP-binding cassette transporter COMATOSE and the multifunctional protein abnormal INFLORESCENCE MERISTEM are required for the production of benzoylated metabolites in Arabidopsis seeds. Plant Physiol. 164, 48-54. Camejo, D., Guzmán-Cedeño, A., Moreno, A., 2016. Reactive oxygen species, essential molecules, during plant-pathogen interactions. Plant Physiol. Biochem. 103, 10-23. Cha, J.-Y., Kim, W.-Y., Kang, S.B., Kim, J.I., Baek, D., Jung, I.J., Kim, M.R., Li, N., Kim, H.-J., Nakajima, M., 2015. A novel thiol-reductase activity of Arabidopsis YUC6 confers drought tolerance independently of auxin biosynthesis. Nat. Commun. 6, 8041. Chang, C.C.C., Ślesak, I., Jordá, L., Sotnikov, A., Melzer, M., Miszalski, Z.,Mullineaux, P.M., Parker, J.E., Karpińska, B., Karpiński, S., 2009. Arabidopsis chloroplastic glutathione peroxidases play a role in cross talk between photooxidative stress and immune responses. Plant Physiol. 150, 670-683. Cheng, N.H., Liu, J.Z., Liu, X., Wu, Q., Thompson, S.M., Lin, J., Chang, J., Whitham, S.A., Park, S., Cohen, J.D., Hirschi, K.D., 2011. Arabidopsis monothiol-glutaredoxin, AtGRXS17, is critical for temperature-dependent postembryonic growth and development via modulating auxin response. J. Biol. Chem. 286, 20398-20406. Corpas, F.J., Barroso, J.B., Palma, J.M., Rodriguez-Ruiz, M., 2017. Plant peroxisomes:a nitro-oxidative cocktail. Redox Biol. 11, 535-542. Corpas, F.J., Gupta, D.K., Palma, J.M., 2015. Production sites of reactive oxygen species (ROS) in organelles from plant cells. In:React Oxyg Species Oxidative Damage W. Plants Stress Springer Cham, pp. 1-22. Cosio, C., Vuillemin, L., DeMeyer, M., Kevers, C., Penel, C., Dunand, C., 2008. An anionic classIII peroxidase from zucchini may regulate hypocotyl elongation through its auxin oxidase activity. Planta 229, 823-836. Cvetkovska, M., Alber, N.A., Vanlerberghe, G.C., 2013. The signaling role of a mitochondrial superoxide burst during stress. Plant Signal. Behav. 8, e22749. Czarnocka, W., Karpiński, S., 2018. Friend or foe? Reactive oxygen species production, scavenging and signaling in plant response to environmental stresses. Free Radic. Biol. Med. 122, 4-20. Das, K., Roychoudhury, A., 2014. Reactive oxygen species (ROS) and response of antioxidants as ROS-scavengers during environmental stress in plants. Front. Environ. Sci. 2, 53. Diaz-Vivancos, P., Barba-Espin, G., Hernandez, J.A., 2013. Elucidating hormonal/ROS networks during seed germination:insights and perspectives. Plant Cell Rep. 32, 1491-1502. Duan, Q., Kita, D., Johnson, E.A., Aggarwal, M., Gates, L., Wu, H.M., Cheung, A.Y., 2014. Reactive oxygen species mediate pollen tube rupture to release sperm for fertilization in Arabidopsis. Nat. Commun. 5, 3129. Dunand, C., Crevecoeur, M., Penel, C., 2007. Distribution of superoxide and hydrogen peroxide in Arabidopsis root and their influence on root development:possible interaction with peroxidases. New Phytol. 174, 332-341. Durme, M.V., Nowack, M.K., 2016. Mechanisms of developmentally controlled cell death in plants. Curr. Opin. Plant Biol. 29, 29-37. El-Maarouf-Bouteau, H., Bailly, C., 2008. Oxidative signaling in seed germination and dormancy. Plant Signal. Behav. 3, 175-182. El-Maarouf-Bouteau, H., Meimoun, P., Job, C., Job, D., Bailly, C., 2013. Role of protein and mRNA oxidation in seed dormancy and germination. Front. Plant Sci. 4, 77. Evans, M.D., Dizdaroglu, M., Cooke, M.S., 2004. Oxidative DNA damage and disease:induction, repair and significance. Mutat. Res. Rev. Mutat. Res. 567, 1-61. Finkelstein, R., Reeves, W., Ariizumi, T., Steber, C., 2008. Molecular aspects of seeddormancy. Ann. Rev. Plant Biol. 59, 387-415. https://doi.org/10.1146/annurev.arplant.59.032607.092740. Foreman, J., Demidchik, V., Bothwell, J.H., Mylona, P., Miedema, H., Torres, M.A., Linstead, P., Costa, S., Brownlee, C., Jones, J.D., Davies, J.M., Dolan, L., 2003. Reactive oxygen species produced by NADPH oxidase regulate plant cell growth. Nature 422, 442-446. Foyer, C.H., Noctor, G., 2013. Redox signaling in plants. Antioxidants Redox Signal. 18, 2087-2090. Graeber, K., Linkies, A., Müller, K., Wunchova, A., Rott, A., Leubner-Metzger, G., 2010. Cross-species approaches to seed dormancy and germination:conservation and biodiversity of ABA-regulated mechanisms and the Brassicaceae DOG1 genes. Plant Mol. Biol. 73, 67-87. Halliwell, B., 2006. Reactive species and antioxidants. redox biology is a fundamental theme of aerobic life. Plant Physiol. 141, 312-322. Halliwell, B., Gutteridge, J.M.C., 1989. Free Radicals in Biology and Medicine. Clarendon Press, Oxford, pp. 450-499. Hossain, M.A., Bhattacharjee, S., Armin, S.M., Qian, P., Xin, W., Li, H.Y., Burritt, D.J., Fujita, M., Tran, L.S., 2015. Hydrogen peroxide priming modulates abiotic oxidative stress tolerance:insights from ROS detoxification and scavenging. Front. Plant Sci. 6, 420. Hulskamp, M., 2004. Plant trichomes:a model for cell differentiation. Nat. Rev. Mol. Cell Biol. 5, 471-480. Ishibashi, Y., Koda, Y., Zheng, S.H., Yuasa, T., Iwaya-Inoue, M., 2013. Regulation of soybean seed germination through ethylene production in response to reactive oxygen species. Ann. Bot. 111, 95-102. Ishibashi, Y., Yamamoto, K., Tawaratsumida, T., Yuasa, T., Iwaya-Inoue, M., 2008. Hydrogen peroxide scavenging regulates germination ability during wheat(Triticum aestivum L.) seed maturation. Plant Signal. Behav. 3, 183-188. Ishibashi, Y., Tawaratsumida, T., Kondo, K., Kasa, S., Sakamoto, M., Aoki, N., Zheng, S.H., Yuasa, T., Iwaya-Inoue, M., 2012. Reactive oxygen species are involved in gibberellin/abscisic acid signaling in barley aleurone cells. Plant Physiol. 158, 1705-1714. Laloi, C., Apel, K., Danon, A., 2004. Reactive oxygen signalling:the latest news. Curr. Opin. Plant Biol. 7, 323-328. Lassig, R., Gutermuth, T., Bey, T.D., Konrad, K.R., Romeis, T., 2014. Pollen tube NAD(P)H oxidases act as a speed control to dampen growth rate oscillations during polarized cell growth. Plant J. 78, 94-106. Lavenus, J., Goh, T., Roberts, I., Guyomarch, S., Lucas, M., De Smet, I., Fukaki, H., Beeckman, T., Bennett, M., Laplaze, L., 2013. Lateral root development in Arabidopsis:fifty shades of auxin. Trends Plant Sci. 18, 450-458. Lee, Y., Rubio, M.C., Alassimone, J., Geldner, N., 2013. A mechanism for localized lignin deposition in the endodermis. Cell 153, 402-412. Leymarie, J., Vitkauskaite, G., Hoang, H.H., Gendreau, E., Chazoule, V., Meimoun, P., Corbineau, F., El-Maarouf-Bouteau, H., Bailly, C., 2012. Role of reactive oxygen species in the regulation of Arabidopsis seed dormancy. Plant Cell Physiol. 53, 96-106. Libik-Konieczny, M., Kozieradzka-Kiszkurno, M., Desel, C., Michalec-Warzecha, Z., Miszalski, Z., Konieczny, R., 2015. The localization of NADPH oxidase and reactive oxygen species in in vitro-cultured Mesembryanthemum crystallinum L. hypocotyls discloses their differing roles in rhizogenesis. Protoplasma 252, 477-487. Lovy-Wheeler, A., Kunkel, J.G., Allwood, E.G., Hussey, P.J., Hepler, P.K., 2006. Oscillatory increases in alkalinity anticipate growth and may regulate actin dynamics in pollen tubes of lily. Plant Cell 18, 2182-2193. Lu, D., Wang, T., Persson, S., Mueller-Roeber, B., Schippers, J.H.M., 2014. Transcriptional control of ROS homeostasis by KUODA1 regulates cell expansion during leaf development. Nat. Commun. 5, 3767. Macpherson, N., Takeda, S., Shang, Z., Dark, A., Mortimer, J.C., Brownlee, C., 2008. NADPH oxidase involvement in cellular integrity. Planta 227, 1415-1418. Mangano, S., Denita Juárez, S., Estevez, J.M., 2016. ROS regulation of polar growth in plant cells. Plant Physiol. 171, 1593-1605. Manzano, C., Pallero-Baena, M., Casimiro, I., DeRybel, B., Orman-Ligeza, B., VanIsterdael, G., Beeckman, T., Draye, X., Casero, P., Del Pozo, J.C., 2014. The emerging role of reactive oxygen species signaling during lateral root development. Plant Physiol. 165, 1105-1119. Marino, D., Dunand, C., Puppo, A., Pauly, N., 2012. A burst of plant NADPH oxidases. Trends Plant Sci. 17, 9-15. McDonald, M.B., 1999. Seed deterioration:physiology, repair and assessment. Seed Sci. Technol. 27, 177-237. Mignolet-Spruyt, L., Xu, E., Idänheimo, N., Hoeberichts, F.A., Mühlenbock, P., Brosché, M., Van Breusegem, F., Kangasjärvi, J., 2016. Spreading the news:subcellular and organellar reactive oxygen species production and signalling. J. Exp. Bot. 67, 3831-3844. Mittler, R., 2017. ROS are good. Trends Plant Sci. 22, 11-19. Monshausen, G.B., Bibikova, T.N., Messerli, M.A., Shi, C., Gilroy, S., 2007. Oscillations in extracellular pH and reactive oxygen species modulate tip growth of Arabidopsis root hairs. Proc. Natl. Acad. Sci. U.S.A. 104, 20996-21001. Monshausen, G.B., Bibikova, T.N., Weisenseel, M.H., Gilroy, S., 2009. Ca2+ regulates reactive oxygen species production and pH during mechano-sensing in Arabidopsis roots. Plant Cell 21, 2341-2356. Moriwaki, T., Miyazawa, Y., Kobayashi, A., Uchida, M., Watanabe, C., Fujii, N., Takahashi, H., 2011. Hormonal regulation of lateral root development in Arabidopsis modulated by MIZ1 and requirement of GNOM activity for MIZ1 function. Plant Physiol. 157, 1209-1220. Müller, K., Linkies, A., Vreeburg, R.A.M., Fry, S.C., Krieger-Liszkay, A., LuebnerMetzger, G., 2009. In vivo cell wall loosening by hydroxyl radicals during cress seed germination and elongation growth. Plant Physiol. 150, 1855-1865. Murmu, J., Bush, M.J., DeLong, C., Li, S., Xu, M., Khan, M., Malcolmson, C., Fobert, P.R., Zachgo, S., Hepworth, S.R., 2010. Arabidopsis basic leucine zipper transcription factors TGA9 and TGA10 interact with floral glutaredoxins ROXY1 and ROXY2 and are redundantly required for anther development. Plant Physiol. 154, 1492-1504. Navrot, N., Rouhier, N., Gelhaye, E., Jacquot, J.-P., 2007. Reactive oxygen species generation and antioxidant systems in plant mitochondria. Physiol. Plant. 129, 185-195. Noctor, G., Reichheld, J.-P., Foyer, C.H., 2018. ROS-related redox regulation and signaling in plants. Semin. Cell Dev. Biol. 80, 3-12. Oracz, K., El-Maarouf-Bouteau, H., Farrant, J.M., Copper, K., Belghazi, M., Job, C., Job, D., Corbineau, F., Bailly, C., 2007. ROS production and protein oxidation as novel mechanism of seed dormancy alleviation. Plant J. 50, 452-465. Oracz, K., Karpiński, S., 2016. Phytohormones signaling pathways and ROS involvement in seed germination. Front. Plant Sci. 7, 864. Passaia, G., Queval, G., Bai, J., Margis-Pinheiro, M., Foyer, C.H., 2014. The effects of redox controls mediated by glutathione peroxidases on root architecture in Arabidopsis thaliana. J. Exp. Bot. 65, 1403-1413. Pautler, M., Eveland, A.L., LaRue, T., Yang, F., Weeks, R., Lunde, C., Je, B.I., Meeley, R., Komatsu, M., Vollbrecht, E., Sakai, H., Jackson, D., 2015. FASCIATED EAR4 encodes a bZIP transcription factor that regulates shoot meristem size in maize. Plant Cell 27, 104-120. Petrov, V.D., Van Breusegem, F., 2012. Hydrogen peroxideea central hub for information flow in plant cells. AoB Plants 2012, ls014. Pierson, E.S., Miller, D.D., Callaham, D.A., Shipley, A.M., Rivers, B.A., Cresti, M., Hepler, P.K., 1994. Pollen tube growth is coupled to the extracellular calcium ion flux and the intracellular calcium gradient:effect of BAPTA type buffers and hypertonic media. Plant Cell 6, 1815-1828. Pospí sil, P., 2016. Production of reactive oxygen species by photosystem II as a response to light and temperature stress. Front. Plant Sci. 7, 1950. Pottosin, I., Velarde-Buendía, A.M., Bose, J., Zepeda-Jazo, I., Shabala, S., Dobrovinskaya, O., 2014. Cross-talk between reactive oxygen species and polyamines in regulation of ion transport across the plasma membrane:implications for plant adaptive responses. J. Exp. Bot. 65, 1271-1283. Rentel, M.C., Knight, M.R., 2004. Oxidative stress-induced calcium signaling in Arabidopsis. Plant Physiol. 135, 1471-1479. Robson, C.A., Vanlerberghe, G.C., 2002. Transgenic plant cells lacking mitochondrial alternative oxidase have increased susceptibility to mitochondria-dependent and independent pathways of programmed cell death. Plant Physiol. 129, 1908-1920. Ros Barceló, A., 2005. Xylem parenchyma cells deliver the H2O2 necessary for lignifications in differentiating xylem vessels. Planta 220, 747-756. Rubio-Diaz, S., Perez-Perez, J.M., Gonzalez-Bayon, R., Munoz-Viana, R., Borrega, N., Mouille, G., Hernández-Romero, D., Robles, P., Höfte, H., Ponce, M.R., Micol, J.L., 2012. Cell expansion-mediated organ growth is affected by mutations in three EXIGUA genes. PLoS One 7, e36500. Schippers, J.H.M., Foyer, C.H., Van Dongen, J.T., 2016. Redox regulation in shoot growth, SAM maintenance and flowering. Curr. Opin. Plant Biol. 29, 121-128. Sharma, P., Jha, A.B., Dubey, R.S., Pessarakli, M., 2012. Reactive oxygen species, oxidative damage, and antioxidative defense mechanism in plants under stressful conditions. J. Bot., Le 2012, 1-26. Singh, R., Singh, S., Parihar, P., Mishra, R.K., Tripathi, D.K., Singh, V.P., Chauhan, D., Prasad, S.M., 2016. Reactive oxygen species (ROS):beneficial companions of plants' developmental processes. Front. Plant Sci. 7, 1299. Steffens, B., Geske, T., Sauter, M., 2011. Aerenchyma formation in the rice stem and its promotion by H2O2. New Phytol. 190, 369-378. Steinhorst, L., Kudla, J., 2013. Calciumda central regulator of pollen germination and tube growth. Biochim. Biophys. Acta 1833, 1573-1581. Stern, R., Kogan, G., Jedrzejas, M.J., Soltés, L., 2007. The many ways to cleave hyaluronan. Biotechnol. Adv. 25, 537-557. Tognetti, V.B., Bielach, A., Hrtyan, M., 2017. Redox regulation at the site of primary growth:auxin, cytokinin and ROS crosstalk. Plant Cell Environ. 40, 2586-2605. Tripathi, S.K., Tuteja, N., 2007. Integrated signaling in flower senescence. Plant Signal. Behav. 2, 437-445. Tripathy, B.C., Oelmüller, R., 2012. Reactive oxygen species generation and signaling in plants. Plant Signal. Behav. 7, 1621-1633. Tsukagoshi, H., 2016. Control of root growth and development by reactive oxygen species. Curr. Opin. Plant Biol. 29, 57-63. Tsukagoshi, H., Busch, W., Benfey, P.N., 2010. Transcriptional regulationof ROS controls transition from proliferation to differentiation in the root. Cell 143, 606-616. Wang, F., Chen, Z.-H., Liu, X., Colmer, T.D., Shabala, L., Salih, A., Zhou, M., Shabala, S., 2017. Revealing the roles of GORK channels and NADPH oxidase in acclimation to hypoxia in Arabidopsis. J. Exp. Bot. 68, 3191-3204. Waszczak, C., Akter, S., Jacques, S., Huang, J., Messens, J., Van Breusegem, F., 2015. Oxidative post-translational modifications of cysteine residues in plant signal transduction. J. Exp. Bot. 66, 2923-2934. Wilkins, K.A., Bancroft, J., Bosch, M., Ings, J., Smirnoff, N., Franklin-Tong, V.E., 2011. Reactive oxygen species and nitric oxide mediate actin reorganization and programmed cell death in the self incompatibility response of Papaver. Plant Physiol. 156, 404-416. Wituszyńska, W., Karpiński, S., 2013. Programmed Cell Death as a Response to High Light, UV and Drought Stress in Plants, pp. 207-245. Xu, L., Zhao, H., Ruan, W., Deng, M., Wang, F., Peng, J., Luo, J., Chen, Z., Yi, K., 2017. ABNORMAL INFLORESCENCE MERISTEM1 functions in salicylic acid biosynthesis to maintain proper reactive oxygen species levels for root meristem activity in rice. Plant Cell 29, 560-574. Xu, R., Li, Y., 2011. Control of final organ size by mediator complex subunit 25 in Arabidopsis thaliana. Development 138, 4545-4554. Yadegari, R., Drews, G.N., 2004. Female gametophyte development. Plant Cell 16, S133-S141. Yamauchi, Y., Furutera, A., Seki, K., Toyoda, Y., Tanaka, K., Sugimoto, Y., 2008. Malondialdehyde generated from peroxidized linolenic acid causes protein modification in heat-stressed plants. Plant Physiol. Biochem. 46, 786-793. Yang, F., Bui, H.T., Pautler, M., Llaca, V., Johnston, R., Lee, B.-H., Kolbe, A., Sakai, H., Jackson, D., 2015. A maize glutaredoxin gene, Abphyl2, regulates shoot meristem size and phyllotaxy. Plant Cell 27, 121-131. Zeng, J., Dong, Z., Wu, H., Tian, Z., Zhao, Z., 2017. Redox regulation of plant stem cell fate. EMBO J. 36, 2844-2855. Zhang, L., Ren, F., Zhang, Q., Chen, Y., Wang, B., Jiang, J., 2008. The TEAD/TEF family of transcription factor Scalloped mediates Hippo signaling in organ size control. Dev. Cell 14, 377-387. |
[1] | Maryam Kazempour Larsary, Hassan Pourbabaei, Ali Salehi, Rasoul Yousefpour, Arshad Ali. Tree-based attributes of large trees more effectively regulate aboveground carbon stock than trait-based ones in temperate deciduous forests [J]. Plant Diversity, 2025, 47(04): 653-665. |
[2] | Fei-Fei Li, Qiang Hao, Xia Cui, Ruo-Zhu Lin, Bin-Sheng Luo, Jin-Shuang Ma. Global invasive alien plant management lists: Assessing current practices and adapting to new demands [J]. Plant Diversity, 2025, 47(04): 666-680. |
[3] | Xiu-Rong Lu, Ming-Chao Liu, Wei-Wei Feng, Bo Qu, Jing-Kuan Wang, Yu-Long Feng. The effects of the invasive plants on soil nematodes vary with the duration of elevated CO2 treatment [J]. Plant Diversity, 2025, 47(04): 681-689. |
[4] | Xinyuan Kuai, Quansheng Fu, Hang Sun, Tao Deng. Expeditionplus: The application of a gridded system in the integration of multidimensional environmental factors [J]. Plant Diversity, 2025, 47(04): 702-708. |
[5] | Jingyang He, Wenjing Yang, Qinghui You, Qiwu Hu, Mingyang Cong, Chao Tian, Keping Ma. Impacts of road networks on the geography of floristic collections in China [J]. Plant Diversity, 2025, 47(03): 403-414. |
[6] | Jing Chen, Jingjing Cao, Binglin Guo, Meixu Han, Zhipei Feng, Jinqi Tang, Xiaohan Mo, Junjian Wang, Qingpei Yang, Yuxin Pei, Yakov Kuzyakov, Junxiang Ding, Naoki Makita, Xitian Yang, Haiyang Zhang, Yong Zhao, Deliang Kong. Increased dependence on mycorrhizal fungi for nutrient acquisition under carbon limitation by tree girdling [J]. Plant Diversity, 2025, 47(03): 466-478. |
[7] | Tao Zhang, Qiang Fang. Consistent spatial-temporal variations of stigmatic pollen load among co-flowering species across six sub-alpine meadows [J]. Plant Diversity, 2025, 47(03): 489-498. |
[8] | Zhi-Li Zhou (周知里), Tial C. Ling, Jian-Li Zhao (赵建立), Xin-Zhi Wang (王欣之), Lin-Lin Wang (王林林), Li Li (李莉), Wen-Jing Wang (王雯婧), Dong-Rui Jia (贾东瑞), Zhi-Kun Wu (吴之坤), Xu-Dong Sun (孙旭东), Yong-Ping Yang (杨永平), Yuan-Wen Duan (段元文). Parallel loss of anthocyanins triggers the incipient sympatric speciation in an alpine ginger [J]. Plant Diversity, 2025, 47(03): 429-439. |
[9] | Shuran Yao, Weigang Hu, Mingfei Ji, Abraham Allan Degen, Qiajun Du, Muhammad Adnan Akram, Yuan Sun, Ying Sun, Yan Deng, Longwei Dong, Haiyang Gong, Qingqing Hou, Shubin Xie, Xiaoting Wang, Jinzhi Ran, Bernhard Schmid, Qinfeng Guo, Karl J. Niklas, Jianming Deng. Distribution, species richness, and relative importance of different plant life forms across drylands in China [J]. Plant Diversity, 2025, 47(02): 273-281. |
[10] | Xian Chen, Pyae Phyo Hein, Mengxue Shi, Fen Yang, Jun Yang, Yao Fu, Xuefei Yang. Diversity and traditional knowledge concerning fodder plants are invaluable assets for enhancing the sustainable management of crop-livestock system of Zhaotong City in the mountainous southwest China [J]. Plant Diversity, 2025, 47(02): 311-322. |
[11] | Jiagang Zhao, Shufeng Li, Jian Huang, Wenna Ding, Mengxiao Wu, Tao Su, Alexander Farnsworth, Paul J. Valdes, Linlin Chen, Yaowu Xing, Zhekun Zhou. Heterogeneous occurrence of evergreen broad-leaved forests in East Asia: Evidence from plant fossils [J]. Plant Diversity, 2025, 47(01): 1-12. |
[12] | Jin-Ru Zhong, Xiao-Fang Jin, Michael C. Orr, Xiao-Qing Li, Yong-Deng He, Sheng-Wei Wang, Qing-Feng Wang, Chun-Feng Yang, Zhong-Ming Ye. The ethics of theft: Reevaluating the impacts of floral larceny on plant reproductive success [J]. Plant Diversity, 2025, 47(01): 148-158. |
[13] | Yuan Wang, Ji Suonan, Kun Liu, Yanni Gao, Sihao Zhu, Qian Liu, Ning Zhao. The third dimension of alpine plant leaf traits is related to cold-tolerance [J]. Plant Diversity, 2025, 47(01): 159-165. |
[14] | Liang Zhang, Zhen-Long Liang, Xue-Ping Fan, Ngan Thi Lu, Xin-Mao Zhou, Hong-Jin Wei, Li-Bing Zhang. The Indo-Burma biodiversity hotspot for ferns: Updated phylogeny, hidden diversity, and biogeography of the java fern genus Leptochilus (Polypodiaceae) [J]. Plant Diversity, 2024, 46(06): 698-712. |
[15] | Hong Qian, Jian Wang, Shenhua Qian, Michael Kessler. Geographic patterns and climatic drivers of the mean genus age of liverworts in North America [J]. Plant Diversity, 2024, 46(06): 723-731. |
Viewed | ||||||
Full text |
|
|||||
Abstract |
|
|||||