PurposeCalcium (Ca 2+ ) is a major structural plant nutrient whose low mobility in the phloem causes deleterious nutritional disorders in non-transpiring organs. Since strontium (Sr 2+ ) and Ca 2+ share many chemical properties, Sr 2+ is frequently used as a tracer to study Ca 2+ cycles in ecosystems. However, the level of agreement between Sr 2+ and Ca 2+ distribution pattern in plants is debatable, and several studies have reported toxic effects of Sr 2+ . Therefore, we investigated Sr 2+ and Ca 2+ uptake rates and distribution pattern to determine how reliably Sr 2+ can be used as a tracer of Ca 2+ in tomato plants (Solanum lycopersicum L.).
MethodsWe conducted six independent experiments of various duration: from a few hours to several weeks, in hydroponic and perlite substrate. We treated plants with either Ca 2+ or Sr 2+ at equivalent concentrations and monitored their accumulation in shoot and fruits.
ResultsUnder short-term exposure (hours), Ca 2+ and Sr 2+ uptake and distribution within the plant were comparable, while the long-term exposure (days and weeks) to 4 mM Sr 2+ reduced transpiration and biomass accumulation. The toxic effect of Sr 2+ was more prominent when growth conditions were favourable. Nonetheless, Sr 2+ accumulated similarly to Ca 2+ in shoot and fruit. Surprisingly, Sr 2+ deposition in tomato fruit cell walls prevented blossom end rot (BER) to the same degree as Ca 2+ .
ConclusionSr 2+ can credibly be used as a tracer of Ca 2+ uptake and allocation in the short-term, making Sr 2+ a powerful tool to study the factors governing Ca 2+ allocation to plant organs, primarily fruit Ca 2+ delivery.