AI Article Synopsis

  • Commercial production of polystyrene (PS) has led to significant environmental pollution, as it is a non-biodegradable plastic that accumulates in various ecosystems.
  • Recent research discovered that the larval gut of yellow mealworms (Tenebrio molitor) can rapidly biodegrade PS, with up to 65% removal of plastic over a few weeks, especially when fed a mix of PS and bran.
  • Experiments demonstrated high survival rates of mealworms fed PS and revealed that different types of PS degrade at varying rates, particularly foams, paving the way for future work on selective breeding for enhanced PS degradation.

Article Abstract

Commercial production of polystyrene (PS) -a persistent plastic that is not biodegradable at appreciable rates in most environments-has led to its accumulation as a major contaminant of land, rivers, lakes, and oceans. Recently, however, an environment was identified in which PS is susceptible to rapid biodegradation: the larval gut of Tenebrio molitor Linnaeus (yellow mealworms). In this study, we evaluate PS degradation capabilities of a previously untested strain of T. molitor and assess its survival and PS biodegradation rates for a range of conditions (two simulated food wastes, three temperatures, seven PS waste types). For larvae fed PS alone, the %PS removed in the short (12-15 h) residence time of the mealworm gut gradually increased for 2-3 weeks then stabilized at values up to 65%. Thirty two-day survival rates were >85% versus 54% for unfed larvae. For mealworms fed ∼10% w/w PS and ∼90% bran, an agricultural byproduct, rates of PS degradation at 25 °C nearly doubled compared to mealworms fed PS alone. Polymer residues in the frass showed evidence of partial depolymerization and oxidation. All of the tested PS wastes degraded, with the less dense foams degrading most rapidly. Mealworms fed bran and PS completed all life cycle stages (larvae, pupae, beetles, egg), and the second generation had favorable PS degradation, opening the door for selective breeding.

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Source
http://dx.doi.org/10.1016/j.chemosphere.2017.10.117DOI Listing

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