Abstract

The identification of the key components in the response to drought stress is fundamental to upgrading drought tolerance of plants. In this study, biochemical responses and leaf gas exchange characteristics of fig (Ficus carica L.) to water stress, short-term elevated CO2 levels and brassinolide application were evaluated. The ‘Improved Brown Turkey’ cultivar of fig was propagated from mature two- to three-year-old plants using cuttings, and transferred into a substrate containing 3:2:1 mixed soil (top soil: organic matters: sand). The experiment was arranged as a nested design with eight replications. To assess changes in leaf gas exchange and biochemical responses, these plants were subjected to two levels of water stress (well-watered and drought-stressed) and grown under ambient CO2 and 800 ppm CO2. Water deficits led to effects on photosynthetic rate, stomatal conductance, transpiration rate, vapour pressure deficit, water use efficiency (WUE), intercellular CO2, and intrinsic WUE, though often with effects only at ambient or elevated CO2. Some changes in content of chlorophyll, proline, starch, protein, malondialdehyde, soluble sugars, and activities of peroxidase and catalase were also noted but were dependent on CO2 level. Overall, fewer differences between well-watered and drought-stressed plants were evident at elevated CO2 than at ambient CO2. Under drought stress, elevated CO2 may have boosted physiological and metabolic activities through improved protein synthesis enabling maintenance of tissue water potential and activities of antioxidant enzymes, which reduced lipid peroxidation.

Highlights

  • Water stress and excessively high temperature are two of the most common yieldlimiting factors for crops in the world

  • Drought stress led to a decline in photosynthesis (A) and intercellular

  • CO2 in ambient conditions, and stomatal conductance at high CO2, and increased stomatal conductance and vapour pressure deficit (VPD) at ambient conditions compared to well-watered conditions

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Summary

Introduction

Water stress and excessively high temperature are two of the most common yieldlimiting factors for crops in the world. The recognition of the key components to water stress is fundamental for upgrading plant drought tolerance [1,2,3]. To maintain their growth, plants have developed multiple tolerance tactics at the molecular, physio-biochemical, and morphological levels to react and adjust in water deficit conditions [2]. Gases do not pass through the leaf cuticle but rather flow into and out of leaves via stomatal pores in the cuticle and epidermis, which are abundant on the lower surface of a leaf in most species. Physiological changes in the guard cells surrounding the stomatal pores account for their opening and closing [5].

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