Detection and Quantification of Dysprosium in Plant Tissues

) as a fluorescence enhancer, we achieved robust emission intensities at 480 and 580 nm, facilitating Dy quantification in complex plant matrices. Additionally, the use of time-resolved fluorescence techniques reduces background autofluorescence from plant tissues, enhancing signal specificity. Validation of the fluorescence method with inductively coupled plasma mass spectrometry (ICP-MS) demonstrated a strong correlation in Dy levels. Greenhouse trials confirmed the method's utility for screening Dy accumulation in living plants and highlighted the potential for rapid stand-off detection. This fluorescence-based approach offers a scalable, efficient tool for identifying Dy-accumulating plants and advances phytomining as a sustainable strategy for REE recovery.