First record of characterization, concentration and distribution of microplastics in coastal sediments of an urban fjord in south west Norway using a thermal degradation method

Plastic waste is of increasing concern in the aquatic environment. A large proportion of plastic waste is generated onshore from where it eventually reaches the marine environment, which is considered the main sink of plastic debris To date there is a substantial lack of knowledge on the composition of these accumulated polymers, their environmental levels and distribution in marine and coastal areas. Current efforts are underway to develop standardized methods to characterize and quantify the occurrence of microplastic in different environmental matrices using microscopy-oriented methods using Fourier Transformed Infra-Red (FTIR) or Raman techniques. However, time-consuming sample preparation, processing and interpretation of complex data limits their use within monitoring programs. As an alternative, a thermal degradation method based on a gas chromatographic mass spectrometer coupled with pyrolysis represents a validated method for qualitative and quantitative polymer analyses. A technique has been developed that combines sample preparation and thermo-analysis for identifying microplastics in samples of marine sediment. Quantification and polymeric composition of plastic particles found in sediment samples taken from ten sites located in Boknafjorden subjected to diverse sources of pollution and anthropogenic pressure were investigated. Plastic microparticles were extracted from 8 kg of wet sediments per site, purified, size-fractionated thorough a set of stainless-steel certified sieves covering the range of 10–250 μm mesh size, pre-concentrated on fiberglass filters and whole filters analyzed by thermal desorption pyrolysis gas chromatography/mass spectrometry. Most of the detected polymers were identified as polypropylene, polyethylene, polyethylene terephthalate, polyvinylchloride, polystyrene or polyamide. In most of the sites, the largest fraction of the extracted micro debris fell in the size range 10–40 μm. Some shifts in size distribution were also observed in some sites and were likely related to the marine sea bottom currents and the influence of specific anthropogenic activities. The adopted thermal degradation method showed good sensitivity, reliability and rapidity and therefore represents a promising technique for microplastic analysis within monitoring activities.