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Batat, D.

Publications and source records attributed to Batat, D..

2 recordsLinked to original sources

Adventitious roots facilitate surface water uptake but only partially sustain transpiration under waterlogging in tomato (Solanum lycopersicum)

waterlogging constrains terrestrial plants by limiting oxygen diffusion in the rhizosphere and altering root-zone physical and chemical properties. However, the extent to which whole-plant responses to waterlogging can be reproduced by oxygen deficiency alone remains unresolved. In tomato (Solanum lycopersicum), waterlogging is commonly associated with adventitious-root formation, yet the functional contribution of these roots to whole-plant water relations has rarely been quantified. Here, we experimentally separated root-zone hypoxia from waterlogging and quantified the contribution of surface-associated adventitious roots to whole-plant transpiration. Using high-resolution gravimetric lysimeters, we monitored transpiration dynamics under two conditions: (i) N2-driven displacement of root-zone O2 under near-field-capacity conditions and (ii) root-zone waterlogging. These measurements were complemented by analyses of soil redox potential and pH, mineral composition, stem anatomy, and genotypic variation among M82, IL11-4, and IL8-1. N2-driven oxygen depletion rapidly reduced rhizosphere O2 concentration and induced a moderate decline in redox potential, accompanied by changes in rhizosphere chemistry and mineral relations. Whole-plant transpiration, however, declined only progressively over several days. Under waterlogging, transpiration declined rapidly in all genotypes, with strong genotype dependence. A transient partial recovery coincided with the appearance of adventitious roots at the soil surface and was followed by renewed decline after drainage. Quantitative analysis indicated that adventitious roots contributed only a limited fraction of daily water uptake, approximately 15% to 20%, which was insufficient to restore pre-waterlogging transpiration or growth. Together, these results show that waterlogging responses were not reproduced by rapid oxygen deprivation alone and that adventitious roots provide limited hydraulic compensation.

plant biology↗

Whole-Plant Physiological Identification and Quantification of Disease Progression

Visual estimates of plant symptoms are traditionally used to quantify disease severity. Yet, the methodologies used to assess these phenotypes are often subjective and do not allow tracking of disease progression from very early stages. Here, we hypothesized that quantitative analysis of whole-plant physiological vital functions can be used to objectively determine plant health, providing a more sensitive way to detect disease. We studied the tomato wilt that is caused by Fusarium oxysporum f. sp. lycopersici. Physiological performance of infected and non-infected tomato plants was compared using a whole-plant pot-based lysimeter functional-phenotyping system in a semi-environmentally controlled greenhouse. Water-balance traits of the plants were measured continuously and simultaneously in a quantitative manner. Infected plants exhibited early reductions in transpiration and biomass gain, which preceded visual disease symptoms. These changes in transpiration proved to be effective quantitative indicators for assessing both plant susceptibility to infection and virulence of the fungus. Physiological changes linked to fungal outgrowth and toxin release contributed to reduced hydraulic conductance during initial infection stages. The functional-phenotyping method objectively captures early-stage disease progression, advancing plant disease research and management. This approach emphasizes the potential of quantitative whole-plant physiological analysis over traditional visual estimates for understanding and detecting plant diseases.

plant biology↗