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Natural abundance δ13C constraints on the detection of microplastic-derived carbon in freshwater environments
Summary
Researchers evaluated whether stable carbon isotope measurements could be used to trace microplastic-derived carbon in freshwater food webs. They found that while one algae species showed significant isotopic shifts when exposed to microplastics, these changes reflected physiological stress rather than actual incorporation of plastic carbon. The study concludes that natural carbon isotope methods have limited practical utility for detecting microplastic signals in freshwater ecosystems under realistic conditions.
Microplastics (MPs) are increasingly recognized as emerging pollutants in freshwater systems. Detecting and tracing MP-derived carbon in aquatic food webs, however, remains unresolved, limiting our understanding of ecological impacts. Here, we evaluate the potential and limitations of natural abundance stable carbon isotope measurements (δ<sup>13</sup>C) as a tool to identify MP signals in freshwater ecosystems. For this purpose, two freshwater algae, Chlorella vulgaris and Chlamydomonas reinhardtii, were exposed under controlled laboratory conditions to one non-biodegradable polymer, low-density polyethylene (LDPE), and two biodegradable polymers, polylactic acid (PLA) and polybutylene adipate-co-terephthalate (PBAT), to assess isotope composition and growth. Laboratory data were complemented by particulate organic carbon (δ<sup>13</sup>C<sub>POC</sub>) measurements from seasonal Danube River campaigns (2023-2024) with modeled predictions based on dissolved organic carbon (δ<sup>13</sup>C<sub>DIC</sub>). MP exposure did not inhibit algae growth, but C. vulgaris exhibited significant (p <0.05) δ<sup>13</sup>C enrichment (+4 to +5 ‰), whereas C. reinhardtii showed no isotopic response. These shifts were unrelated to polymer isotope values and likely reflect indirect physiological stress rather than assimilation of polymer-derived carbon. Complementary binary mixing experiments further confirmed that measurable isotopic shifts occur only at unrealistically low algae-to-MP ratios (≤10:1), underscoring the limited sensitivity of isotope mass balances. Field surveys revealed pronounced seasonal δ<sup>13</sup>C<sub>POC</sub> variability in the Danube, spanning 7.4 ‰ annually. Yet deviations from modeled expectations were inconsistent with MP inputs and instead reflected natural drivers such as productivity and remineralization. Overall, while natural abundance δ<sup>13</sup>C can capture subtle algae responses to MP exposure under laboratory conditions, its diagnostic power for tracing MP-derived carbon in complex freshwater systems appears limited.
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