https://orcid.org/0000-0002-3967-0285
References
- Burgerstein A. Materialien zu einer Monographie betreffend die Erscheinungen der Transpiration der Pflanzen. Verh Zool Ges Wien. 1887;37:1–5.
- Takeda F, Wisniewski ME, Glenn DM. Occlusion of water pores prevents guttation in older strawberry leaves. J Am Soc Hortic Sci. 1991;116:1122–1125. doi:https://doi.org/10.21273/JASHS.116.6.1122.
- Cantamessa S, D’agostino G, Berta G. Hydathode structure and localization in Pteris vittata fronds and evidence for their involvement in arsenic leaching. Plant Biosyst. 2016;150:1208–1215. doi:https://doi.org/10.1080/11263504.2015.1012135.
- Jauneau A, Cerutti A, Auriac M-C, Noël LD. Anatomy of leaf apical hydathodes in four monocotyledon plants of economic and academic relevance. PLoS One. 2020;15:e0232566. doi:https://doi.org/10.1371/journal.pone.0232566.
- Yagi HJ, Nagano A, Kim J, Tamura K, Mochizuki N, Nagatani A, Matsushita T, Shimada T. Fluorescent protein-based imaging and tissue-specific RNA-seq analysis of Arabidopsis hydathodes. J Exp Bot. 2021;72:1260–1270. doi:https://doi.org/10.1093/jxb/eraa519.
- Haberlandt G. Physiological plant anatomy. London: Macmillan and Co; 1914.
- Lepeschkin WW. Über active und passive Wassedrusen und Wasserspalten. Ber Dtsch Bot Ges. 1923;41:298–300.
- Chen C-C, Chen Y-R. Study on laminar hydathodes of Ficus formosana (Moraceae) II. Morphogenesis of hydathodes. Bot Stud. 2006;47:279–292.
- Aloni R. Foliar and axial aspects of vascular differentiation: hypotheses and evidence. J Plant Growth Regul. 2001;20:22–34. doi:https://doi.org/10.1007/s003440010001.
- Aloni R, Schwalm K, Langhans M, Ullrich CI. Gradual shifts in sites of free-auxin production during leaf-primordium development and their role in vascular differentiation and leaf morphogenesis in Arabidopsis. Planta. 2003;216:841–853. doi:https://doi.org/10.1007/s00425-002-0937-8.
- Wang W, Xu B, Wang H, Li J, Huang H, Xu L. YUCCA genes are expressed in response to leaf adaxial-abaxial juxtaposition and are required for leaf margin development. Plant Physiol. 2011;157:1805–1819. doi:https://doi.org/10.1104/pp.111.186395.
- Baylis T, Gierlik I, Sundberg E, Mattsson J. Short internodes/stylish genes, regulators of auxin biosynthesis, are involved in leaf vein development in Arabidopsis thaliana. New Phytol. 2013;197:737–750. doi:https://doi.org/10.1111/nph.12084.
- Robert HS, Grones P, Stepanova AN, Robles LM, Lokerse AS, Alonso JM, Weijers D, Friml J. Local auxin sources orient the apical-basal axis in Arabidopsis embryos. Curr Biol. 2013;23:2506–2512. doi:https://doi.org/10.1016/j.cub.2013.09.039.
- Marin E, Jouannet V, Herz A, Lokerse AS, Weijers D, Vaucheret H, Nussaume L, Crespi MD, Maizel A. miR390, Arabidopsis TAS3 tasiRNAs, and their auxin response factor targets define an autoregulatory network quantitatively regulating lateral root growth. Plant Cell. 2010;22:1104–1117. doi:https://doi.org/10.1105/tpc.109.072553.
- Nakazaki A, Yamada K, Kunieda T, Sugiyama R, Hirai MY, Tamura K, Hara-Nishimura I, Shimada T. Leaf endoplasmic reticulum bodies identified in Arabidopsis rosette leaves are involved in defense against herbivory. Plant Physiol. 2019;179:1515–1524. doi:https://doi.org/10.1104/pp.18.00984.
- Nakazaki A, Yamada K, Kunieda T, Tamura K, Shimada T. Biogenesis of leaf endoplasmic reticulum body is regulated by both jasmonate-dependent and independent pathways. Plant Signal Behav. 2019;14:e1622982. doi:https://doi.org/10.1080/15592324.2019.1622982.
- Pierre-Jerome E, Drapek C, Benfey PN. Regulation of division and differentiation of plant stem cells. Annu Rev Cell Dev Biol. 2018;34:289–310. doi:https://doi.org/10.1146/annurev-cellbio-100617-062459.
- Aloni R. Vascular differentiation and plant hormones. Cham (Switzerland): Springer Nature; 2021.