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Urban air pollution is a crucial global challenge, mainly originating from urbanization and industrial activities, which are continuously increasing. Vegetation serves as a natural air filter for air pollution, but adverse effects on plant health, photosynthesis, and metabolism can occur. Recent omics technologies have revolutionized the study of molecular plant responses to air pollution, overcoming previous limitations. This review synthesizes the latest advancements in molecular plant responses to major air pollutants, emphasizing ozone (O3), nitrogen oxides (NOX), and particulate matter (PM) research. These pollutants induce stress responses common to other abiotic and biotic stresses, including the activation of reactive oxygen species (ROSs)-scavenging enzymes and hormone signaling pathways. New evidence has shown the central role of antioxidant phenolic compound biosynthesis, via the phenylpropanoid pathway, in air pollution stress responses. Transcription factors like WRKY, AP2/ERF, and MYB, which connect hormone signaling to antioxidant biosynthesis, were also affected. To date, research has predominantly focused on laboratory studies analyzing individual pollutants. This review highlights the need for comprehensive field studies and the identification of molecular tolerance traits, which are crucial for the identification of tolerant plant species, aimed at the development of sustainable nature-based solutions (NBSs) to mitigate urban air pollution.

This greenhouse study evaluated the effects of soil enrichment with Pteris vittata rhizosphere bacteria on the growth and accumulation of arsenic in P. vittata grown on a naturally As-rich soil. Inoculations were performed with a consortium of six bacteria resistant to 100 mM arsenate and effects were compared to those obtained on the sterilized soil. Selected bacteria from the consortium were also utilized individually: PVr_9 homologous to Agrobacterium radiobacter that produces IAA and siderophores and shows ACC deaminase activity, PVr_15 homologous to Acinetobacter schindleri that contains the arsenate reductase gene, and PVr_5 homologous to Paenarthrobacter ureafaciens that possesses all traits from both PVr_9 and PVr_15. Frond and root biomass significantly increased in ferns inoculated with the consortium only on non-sterilized soil. A greater increase was obtained with PVr_9 alone, while only an increased root length was found in those inoculated with either PVr_5 or PVr_15. Arsenic content significantly decreased only in ferns inoculated with PVr_9 while it increased in those inoculated with PVr_5 and PVr_15. In conclusion, inoculations with the consortium and PVr_9 alone increase plant biomass, but no increase in As phytoextraction occurs with the consortium and even a reduction is seen with PVr_9 alone. Conversely, inoculations with PVr_5 and PVr_15 have the capacity of increasing As phytoextraction.

The aim of this study was the development of a new multi-analytical approach to evaluate chemical alterations and differences in the element content in relation to arsenic (As) in the As hyperaccumulator fern P. vittata. P. vittata plants were grown on two natural As-rich soils with either high or moderate As (750 and 58 mg/kg). Dried samples from plant tissues were then analysed by means of micro-energy dispersive X-ray fluorescence spectrometry (μ-XRF), attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) and hyperspectral imaging (HSI) with a multivariate approach. The As and micro- and macronutrients content was evaluated by μ-XRF and a significant correlation between As, potassium (K), iron (Fe), calcium (Ca) and manganese (Mn) contents were found at both moderate and high As levels. The same samples were then analysed by ATR-FTIR spectroscopy and HSI (SWIR range, 1000–2500 nm). Interestingly, by FTIR analysis it was found that the main differences between the control and the As-contaminated samples are due to the intensity of the absorption band related to polysaccharides (i.e., cellulose, hemicellulose and pectin), lignin, lipid and amide groups. The same chemical alterations were detected by an HSI analysis and all the FTIR and HSI data were validated by a PCA analysis. These results suggest a possible complexation of As ions with the amide group. Moreover, the proposed μ-XRF, HSI and ATR-FTIR combining approach could be a promising strategy to monitor in-field phytoremediation approaches by directly controlling the As content in plants.

In this study, benchtop micro-X-ray fluorescence spectrometry (µXRF) was evaluated as a green and cost-effective multielemental analytical technique for P. vittata. Here, we compare the arsenic (As) content values obtained from the same samples by µXRF and inductively coupled plasma-optical emissions spectrometry (ICP–OES). To obtain samples with different As concentrations, fronds at different growth time points were collected from P. vittata plants grown on two natural As-rich soils with either high or moderate As (750 and 58 mg/kg). Dried samples were evaluated using multielement-µXRF analysis and processed by PCA. The same samples were then analysed for multielement concentrations by ICP–OES. We show that As concentrations detected by ICP–OES, ranging from 0 to 3300 mg/kg, were comparable to those obtained by µXRF. Similar reliability was obtained for micro- and macronutrient concentrations. A positive correlation between As and potassium (K) contents and a negative correlation between As and iron (Fe), calcium (Ca) and manganese (Mn) contents were found at both high and moderate As. In conclusion, we demonstrate that this methodological approach based on μXRF analysis is suitable for monitoring the As and element contents in dried plant tissues without any chemical treatment of samples and that changes in most nutrient concentrations can be strictly related to the As content in plant tissue.

The reuse of Pteris vittata plants for multiple phytofiltration cycles is a main issue to allow an efficient phytoremediation of arsenic (As)-contaminated groundwater. Here, we assessed the capacity of phytofiltration of P. vittata plants grown for two cycles on naturally As-contaminated drinking water (collected in Central Italy), spaced by a growth cycle on non-contaminated water (N cycle). P. vittata young plants, with extensive frond and root development, were suspended individually in 15 L of water with initial As of 59 µg/L, without any additional treatment or water refilling. During cycle 1, in 45 days P. vittata plants reduced As concentration below 10 µg/L, the allowed EU limits for drinking water. During the subsequent 30 day-N cycle on non-contaminated water, no leaching of As from the roots was observed, while the water pH increased 0.9 Units, but is within the allowed limits. During cycle 2, under the same conditions as cycle 1, As concentration decreased below 10 µg/L in less than seven days. These results show that P. vittata young plants, previously used for the phytofiltration of As, do not extrude As and, when reused, remove As much more rapidly. No additional treatments were required during phytofiltration and thus this represents a sustainable, efficient, and scalable strategy.