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Updated: Jul 15, 2026

Protocol for Microplastics Sampling on the Sea Surface and Sample Analysis
Published on: December 16, 2016
Elucidating microplastic's seasonal occurrence in urban indoor and outdoor aerosol
J Cárdenas-Escudero1, S Deylami2, M López Ochoa2
1Laser Chemistry Research Group, Department of Analytical Chemistry, Faculty of Chemistry, Complutense University of Madrid, Plaza de Ciencias 1, 28040 Madrid, Spain; Analytical Chemistry Department, FCNET, Universidad de Panamá, Ciudad Universitaria, Estafeta Universitaria, 3366, Panamá 4, Panama City, Panama.
Abstract:
This study investigates the seasonal presence of microplastics (MPs) in indoor and outdoor urban aerosols in Madrid, Spain, for the first time ever. Compared with the research conducted in the hydrosphere and lithosphere, atmospheric MPs pollution is considered relatively unexplored. To address this gap, PM10 aerosol samples were collected over one year using the standard EN 12341:2014 method. Two rapid quantification methods based on UV-assisted optical microscopy were used, with and without prior extraction. MPs were characterized morphologically using field-enhanced scanning electron microscopy with energy-dispersive X-ray detection (FE-SEM-EDX) and identified through μRaman spectroscopy and pyrolysis coupled with gas chromatography-mass spectrometry (PyGC-MS). The hybrid single-particle lagrangian integrated trajectory (HYSPLIT) modelling software was used to link MPs potential sources. The study found that indoor MPs exposure (124 ± 25 particles m3/day) were higher than outdoors levels (29 ± 7 particles m3/day). Indoors exposure was 88 ± 32 MPs m3/day during the warm season (April-September) and 122 ± 14 MPs m3/day in the cold season (October-March). Outdoors, exposure was relatively consistent year-round (29 ± 8 and 31 ± 6 particles m3/day, warm and cold respectively). MPs composition in indoor samples and outdoor samples during the warm season was similar, mainly polystyrene (45.8 %), polyethylene (22.8 %), polyethylene terephthalate (20.0 %), and polymethylmethacrylate (11.4 %). However, outdoor MPs during the cold season showed notable differences. Fibres dominated over fragments, mostly smaller than 100 μm. The highest fibre-to-fragment ratios occurred in December outdoors (0.76) and February indoors (0.88). Atmospheric back-trajectory analysis indicated that many MPs likely originated from distant, especially oceanic, sources, confirming their long-range transport. Overall, the findings highlight significant indoor MPs exposure, especially in colder months, and suggest a general increase in MPs exposure over time across both environments.

