in

Medical facemask waste alters detritus decomposition and fungal communities in a freshwater pond


Abstract

Plastic pollution is an ongoing issue in freshwater ecosystems, including that generated from the spike in disposable facemask use during the COVID-19 pandemic. The degradation products of such plastic waste, including plastic leachate compounds and generation of microplastics, have the potential to affect freshwater ecosystem structure and function. We investigated the effects of facemask-derived polypropylene particles of different sizes and their leachates on fungal communities and detritus decomposition in a pond. We further investigated effects of the presence of wood shavings, used to represent a naturally-occurring, highly refractory, organic reference material. Over five weeks, leaf litter mass loss and cotton cellulose tensile strength loss were quantified weekly, and fungal biomass, community composition, and functional gene abundance at two time points. Wood shavings reduced leaf decomposition (-4.4%) relative to controls, while plastics increased decomposition of labile cotton cellulose (+ 6.6%), with the strongest effect from unleached microplastics (+ 22.7%). After 21 days, litter-associated fungal biomass was reduced by the presence of wood shavings (-20.1%) and plastics (-8.6%). Fungal communities differed between wood- and control treatments, and varied widely under plastic exposure. Our findings highlight size- and leachate-dependent effects of facemask-derived plastic particles on freshwater fungal communities and ecosystem functions, which largely contrasted with those of wood.

Data availability

Raw sequencing data is deposited in ENA repository with study accession PRJEB101937 for short read raw sequences ([https://www.ebi.ac.uk/ena/browser/view/PRJEB101937](https:/www.ebi.ac.uk/ena/browser/view/PRJEB101937)) and PRJEB101937 for long read raw sequences ([https://www.ebi.ac.uk/ena/browser/view/PRJEB101937](https:/www.ebi.ac.uk/ena/browser/view/PRJEB101937)). Other data generated and analysed during the current study are available from the corresponding author on reasonable request.

Code availability

Detailed bioinformatics workflows or commands, scripts and parameters can be found in the GitHub repository: (https://github.com/abu85/shotgun_metagenomic_data_analysis).

References

  1. Lebreton, L. & Andrady, A. Future scenarios of global plastic waste generation and disposal. Palgrave Commun. 5, 1–11 (2019).

    Google Scholar 

  2. Yan, H., Cordier, M. & Uehara, T. Future projections of global plastic pollution: Scenario analyses and policy implications. Sustainability 16, 643 (2024).

    Google Scholar 

  3. Benson, N. U., Bassey, D. E. & Palanisami, T. COVID pollution: Impact of COVID-19 pandemic on global plastic waste footprint. Heliyon https://doi.org/10.1016/j.heliyon.2021.e06343 (2021).

    Google Scholar 

  4. Kalantary, R. R. et al. Effect of COVID-19 pandemic on medical waste management: A case study. J. Environ. Health. Sci. Eng. 19, 831–836 (2021).

    Google Scholar 

  5. Roberts, K. P. et al. Increased personal protective equipment litter as a result of COVID-19 measures. Nat. Sustain. 5, 272–279 (2022).

    Google Scholar 

  6. Cordova, M. R., Nurhati, I. S., Riani, E., Iswari, M. Y. & Nurhasanah & Unprecedented plastic-made personal protective equipment (PPE) debris in river outlets into Jakarta Bay during COVID-19 pandemic. Chemosphere 268, 129360 (2021).

    Google Scholar 

  7. Wang, F. et al. Microfiber releasing into urban rivers from face masks during COVID-19. J. Environ. Manage. 319, 115741 (2022).

    Google Scholar 

  8. Worby, C. J. & Chang, H. H. Face mask use in the general population and optimal resource allocation during the COVID-19 pandemic. Nat. Commun. 11, 4049 (2020).

    Google Scholar 

  9. Liu, C., Liu, C., Hotta, Y. & Appleby, D. Comparative analysis of face mask usage and environmental impact in Asian cities during and after the COVID-19 pandemic. Sustainability https://doi.org/10.3390/su16156683 (2024).

    Google Scholar 

  10. Horii, M. Why do the Japanese wear masks? Electronic J. Contemp. Japanese studies (2014).

  11. Andrady, A. L. Persistence of Plastic Litter in the Oceans. In Marine Anthropogenic Litter (eds Bergmann, M. et al.) 57–72 (Springer International Publishing, 2015). https://doi.org/10.1007/978-3-319-16510-3_3.

    Google Scholar 

  12. Zhang, K. et al. Understanding plastic degradation and microplastic formation in the environment: A review. Environ. Pollut. 274, 116554 (2021).

    Google Scholar 

  13. Anene, D. I. et al. Microplastics and chemical additives from disposable face masks: Environmental, human health and behavioural impacts. Sci. Total Environ. 973, 179079 (2025).

    Google Scholar 

  14. Bogush, A. A. & Kourtchev, I. Disposable surgical/medical face masks and filtering face pieces: Source of microplastics and chemical additives in the environment. Environ. Pollut. 348, 123792 (2024).

    Google Scholar 

  15. Azevedo-Santos, V. M. et al. Plastic pollution: A focus on freshwater biodiversity. Ambio 50, 1313–1324 (2021).

    Google Scholar 

  16. López-Rojo, N., Pérez, J., Alonso, A., Correa-Araneda, F. & Boyero, L. Microplastics have lethal and sublethal effects on stream invertebrates and affect stream ecosystem functioning. Environ. Pollut. 259, 113898 (2020).

    Google Scholar 

  17. Huang, Y. et al. Effect of microplastics on ecosystem functioning: Microbial nitrogen removal mediated by benthic invertebrates. Sci. Total Environ. 754, 142133 (2021).

    Google Scholar 

  18. Silva, C. J. M. et al. Microplastics in freshwater sediments: Effects on benthic invertebrate communities and ecosystem functioning assessed in artificial streams. Sci. Total Environ. 804, 467–488 (2022).

    Google Scholar 

  19. Marchant, D. J., Martínez Rodríguez, A., Francelle, P., Jones, J. I. & Kratina, P. Contrasting the effects of microplastic types, concentrations and nutrient enrichment on freshwater communities and ecosystem functioning. Ecotoxicol. Environ. Saf. 255, 114834 (2023).

    Google Scholar 

  20. Wazne, M. et al. Microplastics in freshwater sediments impact the role of a main bioturbator in ecosystem functioning. Environ. Sci. Technol. 57, 3042–3052 (2023).

    Google Scholar 

  21. Kong, Z. H. et al. Microplastics in freshwaters: Comparing effects of particle properties and an invertebrate consumer on microbial communities and ecosystem functions. Ecotoxicol. Environ. Saf. 289, 117697 (2025).

    Google Scholar 

  22. Mora-Teddy, A. K., Closs, G. P. & Matthaei, C. D. Microplastics and riverine macroinvertebrate communities in a multiple-stressor context: A mesocosm approach. Sci. Total Environ. 951, 175456 (2024).

    Google Scholar 

  23. Norhayati, A. M., Matthaei, C. D. & Ingram, T. The impact of microplastics on lake communities: A mesocosm study. Chemosphere 367, 143600 (2024).

    Google Scholar 

  24. Yıldız, D. et al. Effects of a microplastic mixture differ across trophic levels and taxa in a freshwater food web: In situ mesocosm experiment. Sci. Total Environ. 836, 155407 (2022).

    Google Scholar 

  25. Blettler, M. C. M., Abrial, E., Khan, F. R., Sivri, N. & Espinola, L. A. Freshwater plastic pollution: Recognizing research biases and identifying knowledge gaps. Water Res. 143, 416–424 (2018).

    Google Scholar 

  26. Earn, A., Bucci, K. & Rochman, C. M. A systematic review of the literature on plastic pollution in the Laurentian Great Lakes and its effects on freshwater biota. J. Great Lakes Res. 47, 120–133 (2021).

    Google Scholar 

  27. Cera, A. et al. Macroplastics Lakes: Underrepresented Ecol. Problem? Water 15, (2022).

  28. Burns, E. E. & Boxall, A. B. A. Microplastics in the aquatic environment: Evidence for or against adverse impacts and major knowledge gaps. Environ. Toxicol. Chem. 37, 2776–2796 (2018).

    Google Scholar 

  29. Kukkola, A., Krause, S., Lynch, I., Sambrook Smith, G. H. & Nel, H. Nano and microplastic interactions with freshwater biota – Current knowledge, challenges and future solutions. Environ. Int. 152, 106504 (2021).

    Google Scholar 

  30. Webster, J. R. & Benfield, E. F. Vascular plant breakdown in freshwater ecosystems. Ann. Rev. Ecol. Syst. https://doi.org/10.1146/annurev.es.17.110186.003031 (1986).

    Google Scholar 

  31. Gessner, M. O. & Chauvet, E. A case for using litter breakdown to assess functional stream integrity. Ecol. Appl. 12, 498–510 (2002).

    Google Scholar 

  32. Rasmussen, J. B. Estimating terrestrial contribution to stream invertebrates and periphyton using a gradient-based mixing model for δ13C. J. Anim. Ecol. 79, 393–402 (2010).

    Google Scholar 

  33. Benfield, E. F., Fritz, K. M. & Tiegs, S. D. Chapter 27 – Leaf-Litter Breakdown. In Methods in Stream Ecology (Third Edition) (eds Lamberti, G. A. & Hauer, F. R.) 71–82 https://doi.org/10.1016/B978-0-12-813047-6.00005-X (Academic Press, 2017).

  34. Hieber, M. & Gessner, M. O. Contribution of stream detrivores, fungi, and bacteria to leaf breakdown based on biomass estimates. Ecology 83, 1026–1038 (2002).

    Google Scholar 

  35. Kuehn, K. A. Lentic and lotic habitats as templets for fungal communities: Traits, adaptations, and their significance to litter decomposition within freshwater ecosystems. Fungal Ecol. 19, 135–154 (2016).

    Google Scholar 

  36. Suberkropp, K., Arsuffi, T. L. & Anderson, J. P. Comparison of degradative ability, enzymatic activity, and palatability of aquatic hyphomycetes grown on leaf litter. Appl. Environ. Microbiol. 46, 237–244 (1983).

    Google Scholar 

  37. Gessner, M. O., Gulis, V., Kuehn, K. A., Chauvet, E. & Suberkropp, K. Fungal decomposers of plant litter in aquatic ecosystems. Environ. Microb. Relationships https://doi.org/10.1007/978-3-540-71840-6_17 (2007).

    Google Scholar 

  38. Zare-Maivan, H. & Shearer, C. A. Wood decay activity and cellulase production by freshwater lignicolous fungi. International Biodeterioration 24, 459–474 (1988).

    Google Scholar 

  39. Schneider, T. et al. Proteome analysis of fungal and bacterial involvement in leaf litter decomposition. Proteomics 10, 1819–1830 (2010).

    Google Scholar 

  40. Schneider, T. et al. Who is who in litter decomposition? Metaproteomics reveals major microbial players and their biogeochemical functions. ISME J. 6, 1749–1762 (2012).

    Google Scholar 

  41. Baudy, P. et al. Fungal–fungal and fungal–bacterial interactions in aquatic decomposer communities: Bacteria promote fungal diversity. Ecology 102, e03471 (2021).

    Google Scholar 

  42. Pascoal, C. & Cássio, F. Contribution of fungi and bacteria to leaf litter decomposition in a polluted river. Appl. Environ. Microbiol. 70, 5266–5273 (2004).

    Google Scholar 

  43. Tant, C. J., Rosemond, A. D., Helton, A. M. & First, M. R. Nutrient enrichment alters the magnitude and timing of fungal, bacterial, and detritivore contributions to litter breakdown. Freshw. Sci. 34, 1259–1271 (2015).

    Google Scholar 

  44. Suberkropp, K. & Arsuffi, T. L. Degradation, growth, and changes in palatability of leaves colonized by six aquatic hyphomycete species. Mycologia 76, 398–407 (1984).

    Google Scholar 

  45. Jabiol, J. et al. Trophic complexity enhances ecosystem functioning in an aquatic detritus-based model system. J. Anim. Ecol. 82, 1042–1051 (2013).

    Google Scholar 

  46. Wallace, J. B., Webster, J. R. & Cuffney, T. F. Stream detritus dynamics: Regulation by invertebrate consumers. Oecologia 53, 197–200 (1982).

    Google Scholar 

  47. Bundschuh, M., Hahn, T., Gessner, M. O. & Schulz, R. Antibiotic mixture effects on growth of the leaf-shredding stream detritivore Gammarus fossarum. Ecotoxicology 26, 547–554 (2017).

    Google Scholar 

  48. King, J. M., Henshall-Howard, M.-P., Day, J. A. & Davies, B. R. Leaf-pack dynamics in a southern African mountain stream. Freshw. Biol. 18, 325–340 (1987).

    Google Scholar 

  49. Hoffmann, A. Dynamics of fine particulate organic matter (FPOM) and macroinvertebratesin natural and artificial leaf packs. Hydrobiologia 549, 167–178 (2005).

    Google Scholar 

  50. Bertoli, M. et al. Microplastics and leaf litter decomposition dynamics: New insights from a lotic ecosystem (Northeastern Italy). Ecol. Ind. 147, 109995 (2023).

    Google Scholar 

  51. Canhoto, C. & Graça, M. A. S. Leaf barriers to fungal colonization and shredders (Tipula lateralis) consumption of decomposing Eucalyptus globulus. Microb. Ecol. 37, 163–172 (1999).

    Google Scholar 

  52. Teste, F. P., Karst, J., Jones, M. D., Simard, S. W. & Durall, D. M. Methods to control ectomycorrhizal colonization: Effectiveness of chemical and physical barriers. Mycorrhiza 17, 51–65 (2006).

    Google Scholar 

  53. Anttila, A. K. et al. Condensed conifer tannins as antifungal agents in liquid culture. Holzforschung 67, 825–832 (2013).

    Google Scholar 

  54. Capolupo, M., Sørensen, L., Jayasena, K. D. R., Booth, A. M. & Fabbri, E. Chemical composition and ecotoxicity of plastic and car tire rubber leachates to aquatic organisms. Water Res. 169, 115270 (2020).

    Google Scholar 

  55. Sullivan, G. L., Delgado-Gallardo, J., Watson, T. M. & Sarp, S. An investigation into the leaching of micro and nano particles and chemical pollutants from disposable face masks – Linked to the COVID-19 pandemic. Water Res. 196, 117033 (2021).

    Google Scholar 

  56. Li, Z. et al. Plastic leachates lead to long-term toxicity in fungi and promote biodegradation of heterocyclic dye. Sci. Total Environ. 806, 150538 (2022).

    Google Scholar 

  57. Miao, L. et al. Distinct community structure and microbial functions of biofilms colonizing microplastics. Sci. Total Environ. 650, 2395–2402 (2019).

    Google Scholar 

  58. Yang, Y., Liu, W., Zhang, Z., Grossart, H. P. & Gadd, G. M. Microplastics provide new microbial niches in aquatic environments. Appl. Microbiol. Biotechnol. 104, 6501–6511 (2020).

    Google Scholar 

  59. Kettner, M. T., Rojas-Jimenez, K., Oberbeckmann, S., Labrenz, M. & Grossart, H. P. Microplastics alter composition of fungal communities in aquatic ecosystems. Environ. Microbiol. 19, 4447–4459 (2017).

    Google Scholar 

  60. Seeley, M. E., Song, B., Passie, R. & Hale, R. C. Microplastics affect sedimentary microbial communities and nitrogen cycling. Nat. Commun. 11, 1–10 (2020).

    Google Scholar 

  61. Tiegs, S. D., Langhans, S. D., Tockner, K. & Gessner, M. O. Cotton strips as a leaf surrogate to measure decomposition in river floodplain habitats. J. N. Am. Benthol. Soc. 26, 70–77 (2007).

    Google Scholar 

  62. Colas, F. et al. Towards a simple global-standard bioassay for a key ecosystem process: organic-matter decomposition using cotton strips. Ecol. Ind. 106, 105466 (2019).

    Google Scholar 

  63. Frainer, A., Bruder, A., Colas, F., Ferreira, V. & McKie, B. G. Plant litter decomposition as a tool for stream ecosystem assessment. In The Ecology of Plant Litter Decomposition in Stream Ecosystems (eds Swan, C. M. et al.) 483–509 (Springer International Publishing, 2021). https://doi.org/10.1007/978-3-030-72854-0_21.

    Google Scholar 

  64.  Nylund, J.-E. & Wallander, H. 5 Ergosterol Analysis as a Means of Quantifying Mycorrhizal Biomass. in Methods in Microbiology (eds Norris, J. R., Read, D. J. & Varma, A. K.) 24 77–88 (Academic Press, 1992).

  65. Handa, I. T. et al. Consequences of biodiversity loss for litter decomposition across biomes. Nature 509, 218–221 (2014).

    Google Scholar 

  66. Baldy, V., Gessner, M. O. & Chauvet, E. Bacteria, fungi and the breakdown of leaf litter in a large river. Oikos 74, 93–102 (1995).

    Google Scholar 

  67. Newell, S. Y., Moran, M. A., Wicks, R. & Hodson, R. E. Productivities of microbial decomposers during early stages of decomposition of leaves of a freshwater sedge. Freshw. Biol. 34, 135–148 (1995).

    Google Scholar 

  68. Singh, P., Saengerlaub, S., Abas Wani, A. & Langowski, H. Role of plastics additives for food packaging. Pigm. Resin Technol. 41, 368–379 (2012).

    Google Scholar 

  69. Getachew, P. et al. The slip agents oleamide and erucamide reduce biofouling by marine benthic organisms (diatoms, biofilms and abalones). Toxicol. Environ. Health Sci. 8, 341–348 (2016).

    Google Scholar 

  70. Rombouts, J. L., Mos, G., Weissbrodt, D. G., Kleerebezem, R. & Van Loosdrecht, M. C. M. The impact of mixtures of xylose and glucose on the microbial diversity and fermentative metabolism of sequencing-batch or continuous enrichment cultures. FEMS Microbiol. Ecol. 95, fiz112 (2019).

    Google Scholar 

  71. Schaerer, L. et al. Coexistence of specialist and generalist species within mixed plastic derivative-utilizing microbial communities. Microbiome 11, 224 (2023).

    Google Scholar 

  72. Gulis, V. & Suberkropp, K. Interactions between stream fungi and bacteria associated with decomposing leaf litter at different levels of nutrient availability. Aquat. Microb. Ecol. 30, 149–157 (2003).

    Google Scholar 

  73. Romera-Castillo, C., Pinto, M., Langer, T. M., Álvarez-Salgado, X. A. & Herndl, G. J. Dissolved organic carbon leaching from plastics stimulates microbial activity in the ocean. Nat. Commun. 9, 1–7 (2018).

    Google Scholar 

  74. Romera-Castillo, C., Mallenco-Fornies, R. & Saá-Yánez, M. Álvarez-Salgado, X. A. Leaching and bioavailability of dissolved organic matter from petrol-based and biodegradable plastics. Mar. Environ. Res. 176, 105607 (2022).

    Google Scholar 

  75. Sheridan, E. A. et al. Plastic pollution fosters more microbial growth in lakes than natural organic matter. Nat. Commun. 13, 4175 (2022).

    Google Scholar 

  76. Chen, B. et al. Effect of lauric diethanolamide on biodegradability and performance characteristics of mineral hydraulic oil. Int. J. Mater. Prod. Technol. https://doi.org/10.1504/IJMPT.2016.079189 (2016). https://www.inderscienceonline.com/doi/

    Google Scholar 

  77. Do, A. T. N., Ha, Y. & Kwon, J. H. Leaching of microplastic-associated additives in aquatic environments: A critical review. Environ. Pollut. 305, 119258 (2022).

    Google Scholar 

  78. Gulizia, A. M. et al. Understanding plasticiser leaching from polystyrene microplastics. Sci. Total Environ. 857, 159099 (2023).

    Google Scholar 

  79. Wang, K. et al. New Insights into the Long-Term Leaching Process of Dissolved Organic Matter from Microplastics: Dynamic Formation and Transformation Mechanism. Environ. Sci. Technol. 59, 22180–22191 (2025).

    Google Scholar 

  80. Harrison, A. F. The inhibitory effect of oak leaf litter tannins on the growth of fungi, in relation to litter decomposition. Soil Biol. Biochem. 3, 167–172 (1971).

    Google Scholar 

  81. Scalbert, A. Antimicrobial properties of tannins. Phytochemistry 30, 3875–3883 (1991).

    Google Scholar 

  82. Aleklett, K., Ohlsson, P., Bengtsson, M. & Hammer, E. C. Fungal foraging behaviour and hyphal space exploration in micro-structured soil chips. ISME J. 15, 1782–1793 (2021).

    Google Scholar 

  83. Shearer, C. A. & Zare-Maivan, H. In vitro hyphal interactions among wood- and leaf-inhabiting ascomycetes and fungi imperfecti from freshwater habitats. Mycologia https://doi.org/10.2307/3807490 (1988).

    Google Scholar 

  84. Martínez, A., Barros, J., Gonçalves, A. L. & Canhoto, C. Salinisation effects on leaf litter decomposition in fresh waters: Does the ionic composition of salt matter?. Freshw. Biol. 65, 1475–1483 (2020).

    Google Scholar 

  85. Englert, D., Zubrod, J. P., Schulz, R. & Bundschuh, M. Effects of municipal wastewater on aquatic ecosystem structure and function in the receiving stream. Sci. Total Environ. 454–455, 401–410 (2013).

    Google Scholar 

  86. Ferreira, V. et al. A meta-analysis of the effects of nutrient enrichment on litter decomposition in streams. Biol. Rev. 90, 669–688 (2015).

    Google Scholar 

  87. Martínez, A., Larrañaga, A., Pérez, J., Descals, E. & Pozo, J. Temperature affects leaf litter decomposition in low-order forest streams: Field and microcosm approaches. FEMS Microbiol. Ecol. 87, 257–267 (2014).

    Google Scholar 

  88. Kayranli, B., Scholz, M., Mustafa, A. & Hedmark, Å. Carbon storage and fluxes within freshwater wetlands: A critical review. Wetlands 30, 111–124 (2010).

    Google Scholar 

  89. Luo, H. et al. Leaching behavior of fluorescent additives from microplastics and the toxicity of leachate to Chlorella vulgaris. Sci. Total Environ. 678, 1–9 (2019).

    Google Scholar 

  90. Gessner, M. O. Ergosterol as a Measure of Fungal Biomass. In Methods to Study Litter Decomposition: A Practical Guide (eds Bärlocher, F. et al.) 247–255 (Springer International Publishing, 2020). https://doi.org/10.1007/978-3-030-30515-4_27.

    Google Scholar 

  91. Wood, D. E., Lu, J. & Langmead, B. Improved metagenomic analysis with Kraken 2. Genome Biol. 20, 257 (2019).

    Google Scholar 

  92. Põlme, S. et al. FungalTraits: a user-friendly traits database of fungi and fungus-like stramenopiles. Fungal Divers. 105, 1–16 (2020).

    Google Scholar 

  93. Sanyal, A. et al. Aquatic fungal diversity assessment through metagenomics is still limited to current databases. Limnology and Oceanography (2025).

  94. Bates, D., Mächler, M., Bolker, B. M. & Walker, S. C. Fitting linear mixed-effects models using lme4. Journal Stat. Software 67, (2015).

  95. Kuznetsova, A., Brockhoff, P. B. & Christensen, R. H. B. lmerTest package: Tests in linear mixed effects models. J. Stat. Softw. 82, 1–26 (2017).

    Google Scholar 

  96. Oksanen, J. et al. Vegan: Community Ecology Package. (2018).

  97. Valero-Mora, P. M. ggplot2: Elegant graphics for data analysis. J. Stat. Softw. 35212. (2010).

    Google Scholar 

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Acknowledgements

The authors would like to acknowledge support of the National Genomics Infrastructure (NGI)/Uppsala Genome Centre and UPPMAX for providing assistance in massive parallel sequencing and computational infrastructure. Work performed at NGI/Uppsala Genome Centre has been funded by RFI/VR and Science for Life Laboratory, Sweden. The authors also would like to acknowledge SLUBI (SLUs bioinformatics infrastructure) for Bioinformatic support.

Funding

Open access funding provided by Swedish University of Agricultural Sciences. This research was funded by grant NV-03728–17 (awarded to BGM, MB, MNF), from the Swedish Environmental Protection Agency (Naturvårdsverket).

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Z.H.K., B.G.M., M.F., M.B. designed the project. B.G.M., M.F. and M.B. provided funding. M.S. and Z.H.K. collected the samples. M.S. performed measurement of leaf litter decomposition and cotton tensile strength loss. Z.H.K. performed procedures related to DNA metagenomics. R.O. performed ergosterol analyses. S.R. performed chemical screening of leachates. A.B.S. performed bioinformatic analyses. Z.H.K. performed statistical analysis with inputs from B.G.M. Z.H.K. and M.S. wrote the first draft of the manuscript, and all co-authors edited and approved the final version.

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Ze Hui Kong.

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No live plant material was involved in leaf litter collection. No protected or endangered species were involved. This study complied with relevant institutional and national guidelines and regulations, as well as the IUCN Policy Statement on Research Involving Species at Risk of Extinction and the Convention on the Trade in Endangered Species of Wild Fauna and Flora (CITES).

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Kong, Z.H., Stangl, M., Oester, R. et al. Medical facemask waste alters detritus decomposition and fungal communities in a freshwater pond.
Sci Rep (2026). https://doi.org/10.1038/s41598-026-45795-5

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  • DOI: https://doi.org/10.1038/s41598-026-45795-5

Keywords

  • Leaf litter decomposition
  • Cotton tensile strength loss
  • Aquatic fungi
  • Macroplastic
  • Microplastic
  • Plastic leachates


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