# Xylem Parenchyma Anatomy and Gene Expression Patterns Indicate Mechanisms of Cavitation Resistance in Eucalyptus grandis During Drought

## TL;DR

This study explores how Eucalyptus trees resist drought by changing xylem cell structure and gene activity to prevent water transport failure.

## Contribution

The study identifies anatomical and gene expression changes in xylem parenchyma that enhance drought resistance in Eucalyptus grandis.

## Key findings

- Smaller ray parenchyma cells increase ray-vessel contacts, reducing isolated vessels.
- Upregulated genes include aquaporins, lipid transfer proteins, and triacylglycerol biosynthesis enzymes.
- Osmotic regulation genes suggest solute-mediated mechanisms for refilling embolized vessels.

## Abstract

Tree survival under drought conditions depends on the ability to maintain functional xylem and avoid hydraulic failure due to cavitation. Although xylem parenchyma are key sites of metabolic activity in angiosperm wood, the anatomical and gene expression responses of this cell type to drought stress remain poorly characterized. This study investigated how
Eucalyptus grandis
W. Hill ex Maiden modifies parenchyma anatomy and gene expression under water deficit to enhance cavitation resistance. Under controlled drought conditions, plants produced significantly smaller ray parenchyma cells with increased frequency. This arrangement reduced the proportion of isolated vessels through elevated ray‐vessel contacts, likely enhancing solute delivery to stressed conduits. Transcriptomic analysis revealed upregulation of aquaporins, lipid transfer proteins, and enzymes involved in triacylglycerol biosynthesis, supporting roles in water transport and nanobubble stabilization under negative pressure. In parallel, genes associated with osmotic regulation, including various sugars, myo‐inositol, and metal ion transporters, were also induced, indicating putative solute‐mediated mechanisms for refilling embolized vessels. This transcriptomic response appears to be primarily triggered by oxidative and hypoxic stress signals. Collectively, these results indicate that xylem parenchyma contribute to embolism resistance by actively redistributing water and supporting hydraulic stability during drought. This work provides mechanistic insights into tree drought adaptation, with implications for forest management and climate resilience strategies.