A New Microscopy Toolbox Reveals How Microplastics Meet the Guts of Freshwater Animals
Tiny plastic particles may be accumulating in the mud beneath rivers and lakes, but scientists still have limited ability to see exactly what happens after bottom-dwelling animals swallow them. A new study from researchers at the University of Bayreuth in Germany has developed a set of laboratory techniques designed to preserve both animal tissues and microplastic particles during microscopic analysis. The toolbox allows researchers to examine ingested polystyrene particles in two important freshwater invertebrates: the blackworm, Lumbriculus variegatus, and larvae of the harlequin fly, Chironomus riparius. The methods combine conventional histology, frozen tissue sectioning and scanning electron microscopy, creating a detailed way to investigate whether plastic simply passes through the gut, presses against intestinal tissues or moves into the body.
Microplastics are generally defined as plastic particles smaller than 5 millimeters, although the particles used in this study were far smaller. They were spherical polystyrene particles with a size distribution reaching a 90th-percentile diameter of 10.4 micrometers—roughly comparable to the width of some human cells. Such particles can enter freshwater environments as fragments of larger plastic waste or through other routes, and sediments can act as a long-term sink. Organisms that live in or feed directly from sediment are consequently exposed at the point where particles settle. Both L. variegatus, an oligochaete worm, and C. riparius, a nonbiting midge whose larvae inhabit sediments, are widely used in ecotoxicology. Previous studies have linked microplastic exposure in these animals to effects including oxidative stress, inflammation, intestinal damage and depletion of energy reserves. Yet the biological mechanisms behind those effects remain uncertain because researchers have struggled to locate the particles precisely in relation to gut tissues.
The central technical problem is that many standard tissue-processing methods can destroy the evidence scientists are trying to observe. To prepare tissue for paraffin histology, laboratories commonly use xylene as a clearing agent, allowing alcohol-dehydrated tissue to become compatible with molten paraffin. But xylene can dissolve or damage some polymers, including polystyrene. Standard protocols for scanning electron microscopy may also use acetone during dehydration, which can alter the surface or shape of microplastic particles. If a particle disappears or changes before it reaches the microscope, researchers can no longer tell whether it was absent from the animal or lost during preparation. The Bayreuth team therefore adapted the protocols to avoid plastic-damaging reagents. Isopropanol replaced xylene during paraffin processing and deparaffinization, while ethanol was used for dehydration before scanning electron microscopy.
The researchers first reared the two organisms under controlled laboratory conditions and then exposed them to fluorescently labeled polystyrene particles for 48 hours. The experimental concentration was 1 gram per liter, deliberately much higher than typical environmental concentrations. This was not intended as a realistic toxicity test but as a method-development experiment in which particles needed to be easy to locate. The particles carried rhodamine B, a fluorescent dye, so that they could be distinguished from food and sediment under a fluorescence microscope. The authors caution that fluorescent particles are useful for tracking uptake and distribution but should not automatically be used in toxicity experiments, because dyes can potentially leach from particles and contribute to biological effects. In future studies, the particles could instead be identified with chemical techniques such as Raman spectroscopy or Fourier-transform infrared imaging.
For paraffin sections, the team fixed the animals, dehydrated them through alcohol solutions and used isopropanol as the transition medium before embedding them in paraffin. They cut sections only 5 micrometers thick, thin enough to resolve major anatomical structures while retaining information about the digestive tract. The tissue was stained with hematoxylin and eosin, a classic combination in which hematoxylin highlights nuclei and other acidic structures while eosin stains much of the cytoplasm and connective tissue. The resulting sections were comparable in quality to those produced with conventional xylene-based protocols. In the midge larvae, researchers could identify the salivary glands, fat body, gut epithelium and nervous system. In the worms, the sections preserved gut epithelial cells, muscle tissue, blood vessels and parts of the nervous system. The work therefore provides a general tissue map against which the location of ingested particles can be compared.
An unexpected obstacle came from the sediment itself. Quartz sand, routinely used in cultures and toxicity tests, was often swallowed by the sediment-dwelling animals. During microtome sectioning, those hard grains damaged disposable blades and disrupted the tissue, particularly in the gut. The researchers found that animals reared with wood chips instead of quartz sand produced much cleaner sections. This change was not a biological treatment intended to mimic a natural habitat; it was a practical measure to prevent physical damage during sample preparation. The team also identified a separate artifact caused by slide drying. If sections of C. riparius remained too long on a heated plate or were exposed to excessive heat, the midgut could balloon and the gut epithelium could rupture. Without careful control, such damage might be mistaken for an effect of microplastic exposure. The finding emphasizes that preparation artifacts can imitate pathology and must be controlled before biological conclusions are drawn.
The fluorescent particles were visible in unstained paraffin sections from exposed animals of both species and were absent from controls. After the full hematoxylin-and-eosin procedure, however, the fluorescent signal disappeared, even though bright-field images still revealed spherical particles in the digestive tract. The result suggests that the staining sequence reduced or removed the rhodamine signal rather than relocating the particles. In cryosections, the particles remained fluorescent after staining, although their signal was weaker. For this approach, the animals were rapidly frozen, embedded in 6 percent gelatin and cut into 20-micrometer sections at approximately minus 20 degrees Celsius. Cryosections generally preserve tissue structure less effectively than paraffin sections, but they can be produced quickly and have an important analytical advantage: they can be used for methods that depend on retaining chemical information. Because the samples were not fixed, they could potentially support matrix-assisted laser desorption/ionization mass spectrometry imaging, Raman imaging and Fourier-transform infrared analysis.
The third component of the toolbox used scanning electron microscopy to examine the gut at much higher magnification. Instead of acetone, the specimens were dehydrated through ethanol and then dried using critical point drying, a process that replaces liquid within the specimen with carbon dioxide before carefully removing it. This reduces the surface tension forces that can collapse delicate biological structures during ordinary drying. After drying, the animals were dissected, mounted on conductive stubs and coated with thin layers of carbon and platinum. The resulting images showed the digestive systems of both species without major drying artifacts. In C. riparius, the researchers could see particles embedded in a food bolus and enclosed by the peritrophic membrane, a protective, semipermeable structure that separates gut contents from epithelial cells. At higher magnification, microvilli and the interface between the particles and gut lining remained visible. In L. variegatus, the method also revealed particle-filled regions and the zone where ingested polystyrene contacted the gut epithelium. No particles were detected in control animals, indicating that the preparation process did not introduce obvious cross-contamination.
The study does not establish that the particles crossed the gut wall or caused a particular toxic effect. Instead, it supplies the missing technical foundation needed to answer those questions more reliably. A particle inside the digestive tract is not necessarily a particle inside the tissue, and fluorescence alone can be misleading if dye separates from the plastic. The researchers therefore envision combining the toolbox with chemical imaging, immunohistochemistry and elemental analysis. Paraffin sections provide strong tissue preservation and can support conventional staining or investigations of stress-related markers. Cryosections offer access to molecular and chemical mapping, including the detection of unlabeled particles under more environmentally realistic conditions. Scanning electron microscopy adds three-dimensional, ultrastructural information about particle-contact zones. Together, these approaches could help distinguish simple gut passage from persistent attachment, cellular injury or true translocation into tissues. By replacing plastic-damaging solvents with compatible alternatives, the work makes it possible to inspect both sides of the interaction—the animal’s biology and the particle’s physical integrity—without sacrificing one to study the other.
Subject of Research: Microplastic–tissue interactions in benthic freshwater invertebrates
Subject of Research: Technology and Engineering
Article Title: Development of a toolbox for the analysis of microplastic-tissue interactions in two benthic freshwater organisms
Article References: Schmitt, J., Ritschar, S., Schott, M., Römpp, A., & Laforsch, C. (2026). Development of a toolbox for the analysis of microplastic-tissue interactions in two benthic freshwater organisms. Microplastics and Nanoplastics, 6(1), Article 8. https://doi.org/10.1186/s43591-025-00171-4
Image Credits: AI Generated
DOI: 10.1186/s43591-025-00171-4
Keywords: microplastics, freshwater invertebrates, histology, paraffin sectioning, cryosectioning, scanning electron microscopy, polystyrene, tissue interactions
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SCIENMAG. (August 27, 2026). New toolbox analyzes microplastic-tissue interactions in two freshwater benthic organisms. https://scienmag.com/new-toolbox-analyzes-microplastic-tissue-interactions-in-two-freshwater-benthic-organisms/
SCIENMAG. “New toolbox analyzes microplastic-tissue interactions in two freshwater benthic organisms.” Scienmag, 27 August 2026, https://scienmag.com/new-toolbox-analyzes-microplastic-tissue-interactions-in-two-freshwater-benthic-organisms/. Accessed 27 August 2026.
SCIENMAG. “New toolbox analyzes microplastic-tissue interactions in two freshwater benthic organisms.” Scienmag. August 27, 2026. https://scienmag.com/new-toolbox-analyzes-microplastic-tissue-interactions-in-two-freshwater-benthic-organisms/
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