Formation of Zn and Pb sulfides in a redox-sensitive modern system due to high atmospheric fallout
Beata Smieja-Kr\'ol, Miros{\l}awa Pawlyta, Mariola, K\k{a}dzio{\l}ka-Gawe{\l}, Barbara Fia{\l}kiewicz-Kozie{\l}

TL;DR
This study investigates the formation of zinc and lead sulfides in a modern peat system influenced by atmospheric fallout, revealing complex mineral structures and organic interactions that inform both pollution impact and ancient ore deposit formation.
Contribution
It provides detailed microscopic and chemical analysis of metal sulfide formation in a modern environment, highlighting human impact on mineralization processes.
Findings
Zn and Pb sulfides form within 15 cm of peat surface
Complex polycrystalline sphalerite structures develop in decades
Pb sulfides are crystalline and defect-free, influenced by organic matter
Abstract
The study shows that the air-derived metal enrichment (up to 2.3 g Zn kg-1, 1.1 g Pb kg-1, and 62 mg Cd kg-1) is retained in a thin layer (~30 cm) around 10-15 cm below the peat surface. A combination of focused ion beam (FIB) technology and scanning (SEM) and transmission (TEM) electron microscopy reveals that micrometric spheroids are most characteristic for ZnS and (Zn,Cd)S, although the sulfides readily form pseudomorphs after different plant tissues resulting in much larger aggregates. The aggregates have a complex polycrystalline sphalerite structure much more advanced than typically obtained during low-temperature synthesis or observed in other modern occurrences. Platy highly-disordered radially-aggregated submicrometre crystals develop within the time constraints of several decades in the cold (~15{\deg}C) and acid (pH 3.4-4.4) peat. The less abundant Pb sulfides occur as…
Peer Reviews
No public reviews on file for this paper yet. If you reviewed it on a platform where reviews are public (OpenReview, ICLR, NeurIPS, ICML), you can paste yours below so the community can read it here.
Videos
No videos yet. Explain this paper in a talk, walkthrough, or lecture? Add one.
