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P26 | Using Histology to Detect and Quantify Microplastics in the Coanocytes of the Sponge Paraleucilla Magna Kalutau Et Al., 2004 (porifera, Calcarea)
Summary
Scientists developed a new lab technique to actually see and count microplastic particles inside the cells of sea sponges, which filter huge amounts of ocean water for food. Using this method, they confirmed that sponges exposed to microplastics absorbed significantly more plastic particles than unexposed ones—making these sponges a useful early-warning tool for tracking how microplastics build up in marine life. Since these tiny plastics move up the food chain and end up in seafood, better ways to detect them in ocean organisms could help researchers understand how much plastic exposure eventually reaches humans.
The ingestion of microplastics (MPs) by marine invertebrates can disrupt essential biological processes, including growth, feeding, reproduction, respiration, and immune responses (Stephanie et al., 2013). Although environmental MP concentrations often exceeded those found in sponge tissues, filter-feeding sponges may possess resistance mechanisms and/or active expulsion pathways, enabling survival in polluted habitats and making them valuable models for assessing particle-related impacts on marine life (Aguilo-Arce et al., 2025). Detecting MPs within biological tissues remains challenging, as standard histological procedures are largely incompatible with MP visualization (Aguilo-Arce et al., 2025). In this study, we validated a novel histological approach based on Technovit 8100 embedding to localize and quantify fluorescent MPs within the body plan and choanocytes of the calcareous sponge Paraleucilla magna. This method allowed reliable detection of MPs at both tissue and cellular levels, overcoming limitations of conventional paraffin-based protocols. Quantitative image analysis revealed a significant increase in MP-occupied area in exposed sponges compared to controls. Statistical evaluation using both parametric and non-parametric tests confirmed highly significant differences in the internalized particle load between control and MP-treated groups (p˂0.001). Overall, this validated histological tool provides a robust, reproducible tool for detecting and quantifying MPs in sponges, enabling high-resolution assessment of particle internalization dynamics and supporting the use of the calcareous sponge P. magna as a sensitive model for evaluating microplastic impacts in marine filter-feeders.