Utecht Steve, Krause Stefan, Schuetz Tobias
Spatial and Environmental Sciences, Trier University, Campus II, 54286, Trier, Germany.
School of Geography, Earth and Environmental Sciences, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.
Environ Monit Assess. 2025 Jul 21;197(8):934. doi: 10.1007/s10661-025-14317-7.
Microplastics (MPs) are pervasive and widespread pollutants penetrating ecosystems worldwide, including aquatic environments and sediments. The lack of standardised evaluation procedures and limited sample throughput hampers accurate assessment of global MP pollution. High-throughput analytical methods are crucial for advancing our understanding of MP cycling in the environment. This study compares MP observations by confocal micro-Raman spectroscopy and Nile Red-assisted fluorescence microscopy to evaluate their effectiveness for high-throughput MP analysis using the percentage differences (%DIF) between the results of the two methods. The results show the influence of particle size on the detected percentage differences and demonstrate that both methods deliver better matching results at smaller particle sizes. The overall percentage difference in the number of detected MP counts between the two methods is 421%, with variations ranging over three orders of magnitude depending on morphological characteristics (particles and fibres) and particle size, whereas the analysis of the distribution of the detected polymers across the particle size fractions does not indicate that specific polymer types influence the observed %DIF between the two methods in this study. The combination of the Fenton reagent's limited organic matter removal and the resulting increased risk of false-positive MP detection, along with Raman spectroscopy's ability to reliably distinguish MPs from organic components, offers opportunities for data validation and correction to enhance accuracy and reliability of the results. This study contributes to the development of robust methods for high-throughput MP analysis, enabling improved spatial and temporal monitoring of its fate and transport in natural fluxes.
微塑料(MPs)是普遍存在且广泛分布的污染物,已渗透到全球生态系统中,包括水生环境和沉积物。缺乏标准化的评估程序以及有限的样品通量阻碍了对全球微塑料污染的准确评估。高通量分析方法对于深化我们对微塑料在环境中循环的理解至关重要。本研究比较了共聚焦显微拉曼光谱法和尼罗红辅助荧光显微镜法对微塑料的观测结果,以使用两种方法结果之间的百分比差异(%DIF)来评估它们在高通量微塑料分析中的有效性。结果显示了粒径对检测到的百分比差异的影响,并表明两种方法在较小粒径下能提供更好的匹配结果。两种方法检测到的微塑料数量的总体百分比差异为421%,其变化范围跨越三个数量级,具体取决于形态特征(颗粒和纤维)以及粒径,而对检测到的聚合物在粒径分级中的分布分析表明,在本研究中特定的聚合物类型并未影响两种方法之间观测到的%DIF。芬顿试剂去除有机物能力有限以及由此导致的微塑料假阳性检测风险增加,再加上拉曼光谱能够可靠地区分微塑料与有机成分,为数据验证和校正提供了机会,以提高结果的准确性和可靠性。本研究有助于开发用于高通量微塑料分析的可靠方法,从而改进对其在自然通量中归宿和迁移的时空监测。