Weikun Xu, Qi Wang, Shengchao Yao, Naiyu Xie, Linjie Jin, Yetong Shao, Lu Zhang, Mengyang Liu, Anqi Xie, Wei Gao, Xuguang Chen, Kenneth M Y Leung, Yuefei Ruan
Chlorinated paraffins (CPs) are high-production-volume industrial chemicals, yet their occurrence and distribution in deep-ocean basins remain poorly understood. Here, this study investigated 771 homologues of CPs with various carbon chain lengths (i.e., C6-C40), including very short-chain (vSCCPs, C6-C9; semi-quantified), short-chain (SCCPs, C10-C13), medium-chain (MCCPs, C14-C17), long-chain (LCCPs, C18-C20), and very long-chain CPs (vLCCPs, C21-C40; semi-quantified) in surface sediment samples collected from 17 sites in the Indian Ocean basins using high-resolution mass spectrometry. CPs were detected in 65% of the samples, with total concentrations of 15-100 ng/g dry weight (dw) (mean: 40 ± 27 ng/g dw). MCCPs (51%) and SCCPs (43%) predominated the homologue profiles, while vSCCPs, LCCPs, and vLCCPs were also frequently semi-quantitatively detected, indicating the widespread dispersion of lesser-monitored CP classes into deep-sea sediments. A clear spatial fractionation was observed: Western sediments (Arabian Sea) were enriched in heavier CP groups (MCCPs, 64%; C14-C15 homologues), whereas eastern sediments showed higher proportions of lighter CP groups (SCCPs, 53%; C10-C11 homologues). The positive correlation between concentrations of CPs and total organic carbon suggests that organic matter and particle-associated transport play an important role in CP accumulation, whereas the lack of a depth trend indicates that overlying water depth alone is not a primary predictor of sedimentary CP burdens. This study provides first-hand baseline data on C6-C40 CPs in deep-sea sediments, revealing the previously unrecognized presence of vSCCPs and vLCCPs in remote basins, and highlighting the need to include homologue-specific transport and deep-sea sequestration in future CP monitoring and risk assessment frameworks.