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Mangroves have evolved at least 27 times across ~20 plant families to survive coastal. To environments characterized by high salinity, inundation, intense light, and strong winds survive these extreme conditions, mangroves exhibit a variety of physiological strategies to tolerate the low osmotic potentials associated with saltwater inundation. Because low osmotic potentials are counterbalanced by high turgor pressure, saltwater exposure exerts mechanical demands on cells. Analyzing 34 mangrove species and 33 closely related inland taxa from 17 plant families, we show that compared to their inland relatives, mangroves have unusually small leaf epidermal pavement cells and thicker cell walls, which together confer greater mechanical strength and tolerance to low osmotic potentials. However, mangroves do not exhibit smaller, more numerous stomata that enable higher photosynthetic rates , suggesting selection on biomechanical integrity rather than on gas exchange capacity. Notably, mangroves break the allometric scaling between the sizes of epidermal pavement cells and stomata typically seen in land plants, highlighting that strong selection in saline habitats can override genome size–mediated scaling rules. Phylogenetic comparative analyses revealed repeated convergent evolution of cell traits across independent transitions from inland to coastal habitats. These anatomical changes constitute a simple but effective adaptation to salt stress. Our findings underscore the role of biomechanics in driving convergent evolution of cell traits and suggest that manipulating cell size and wall properties could be a promising strategy to engineering salt-tolerant plants. 

• Drought-induced xylem embolism is a primary cause of plant mortality. Although ~70% of cycads are threatened by extinction and extant cycads diversified during a period of increasing aridification, the vulnerability of cycads to embolism spread has been overlooked. • We quantified the vulnerability to drought-induced embolism, pressure-volume curves, in situ water potentials, and a suite of xylem anatomical traits of leaf pinnae and rachises for 20 cycad species. We tested whether anatomical traits were linked to hydraulic safety in cycads. • Compared to other major vascular plant clades, cycads exhibited similar embolism resistance to angiosperms and pteridophytes but were more vulnerable to embolism than non-cycad gymnosperms. All 20 cycads had both tracheids and vessels, the proportions of which were unrelated to embolism resistance. Only vessel pit membrane fraction was positively correlated to embolism resistance, contrary to angiosperms. Water potential at turgor loss was significantly correlated to embolism resistance among cycads. • Our results show that cycads exhibit low resistance to xylem embolism and that xylem anatomical traits–particularly vessels–may influence embolism resistance together with tracheids. This study highlights the importance of understanding the mechanisms of drought resistance in evolutionarily unique and threatened lineages like the cycads.