Primo Proietti

Salt stress is one of the preeminent abiotic stressors capable of strongly impacting crop productivity and quality. Within the array of strategies garnering interest in safeguarding crops against abiotic stresses, the use of plant biostimulants is emerging as a noteworthy avenue. For the above, there is an increasing interest in finding new plant extracts showing biostimulating effects in crops. In the present study, the efficacy of an aqueous extract from an aquatic species, the duckweed (Lemna minor L.), was assessed in olive plants (cv. Arbequina) grown in hydroponics and exposed to severe saline stress (150 mM NaCl). Salt stress caused considerable diminutions in biomass production, leaf net photosynthesis (Pn), leaf transpiration rate (E), and stomatal conductance (gs). The application of the duckweed extract resulted in a notable plant functionality recovery and counteracted the detrimental effects of the NaCl stress. Indeed, the plants stressed with NaCl and treated with the extract showed enhanced physiological and biometric traits compared to samples treated with NaCl alone. In particular, the duckweed extract improved photosynthetic activity and stomatal conductance, reduced the intercellular CO2 concentration, and ameliorated other physiological and morphological parameters. All these benefits influenced the whole plant growth, allowing samples treated with the extract to maintain a similar performance to that exhibited by the Control plants.

In vitro culture, ensuring rapid multiplication and production of plant material under aseptic conditions, represents an excellent tool for ex-situ conservation of tree species biodiversity and can be used for the conservation, among others, of endangered and rare crops. Among the Pyrus communis L. cultivars that have been abandoned over the years due to changed cultivation requirements, but which are still used today in breeding programs, there is the ‘Decana d’inverno’. Pear is generally considered a recalcitrant species for in vitro propagation due to weak multiplication rate, hyperhydricity, and susceptibility to phenolic oxidation. Therefore, the use of natural substances like neem oil (although little explored) represents one of the options to improve the in vitro plant’s tissue culture. In this context, the aim of the present work was to evaluate the effect of adding neem oil (0.1 and 0.5 m L L−1) to the growth substrate in order to optimise the in vitro culture of the ancient pear tree cultivar ‘Decana d’inverno’. The neem oil addition resulted in an increase in the number of shoots produced especially at both concentrations used. On the contrary, an increase in length of proliferated shoots was observed only with the addition of 0.1 mL L−1. The neem oil addition did not affect the explants viability, fresh and dry weights. Therefore, the present study demonstrated for the first time the possibility of using neem oil to optimise the in vitro culture of an ancient pear tree cultivar.