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The distribution and metabolism of hexabromocyclododecane isomers varies in the tissues of Nibea albiflora
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This paper is not about microplastics — it investigates how hexabromocyclododecane (HBCD), a brominated flame retardant, accumulates in different tissues of a marine fish species, and how it transfers from parent fish to offspring, including the finding that beta and gamma isomers convert to the more persistent alpha-HBCD within fish tissues.
Hexabromocyclododecanes (HBCDs), as brominated flame retardants, have increasingly drawn concern due to their detection in various marine organisms in recent years. The present test investigated the selective accumulation, depuration, and bioisomerization of HBCDs in different tissues and organs of Nibea albiflora , as well as the genetic metabolic behavior of HBCDs between parents and offspring. In a semi-static water environment, N. albiflora were exposed to individual HBCD diastereoisomers ( α -HBCD, β -HBCD, or γ -HBCD) at a concentration of 0.4 μg/L for bioaccumulation, followed by clean food for depuration. During the exposure period, the highest concentrations of these HBCDs were observed in the intestine and gill of N. albiflora . α -HBCD was detected in all exposure groups, suggesting that both β -HBCD and γ -HBCD could be bioisomerized to α -HBCD in N. albiflora . In addition, there was no bioisomerization of α -HBCD to either β -HBCD or γ -HBCD, and there was no bioisomerization between β -HBCD and γ -HBCD. The half-lives ( t 1/2 ) were variable among different diastereoisomers, following an order of α -HBCD > γ -HBCD > β -HBCD. The most rapid depuration rate of HBCDs was discovered in the liver while muscle showed the least. Additionally, prior to spawning, the parent fish were exposed to contaminated feed (silkworms sprayed with 200 μL of a 30 μg/mL HBCD solution) for 6 days. By comparing the HBCDs concentrations in the maternal gonad, fertilized eggs, hatching eggs, larvae, and juveniles, it was determined that the maternal transfer coefficients for HBCDs were approximately 1, indicating dynamic equilibrium of HBCDs throughout the process from maternal tissue to progeny development. Differences in HBCDs pattern between organs observed in the experiment support a proposal of an organ-specific diastereomer accumulation.
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