Apportioning sources of natural and anthropogenic organic matter in sediment from Lake Shihwa: An integrated approach using molecular ratios and compound-specific stable-isotope analysis.

We tested an integrated multi-isotopic analysis framework to quantitatively estimate anthropogenic organic matter (OM) loads in different land-use types of a watershed (Lake Shihwa, South Korea). The isotopic signatures of increased bulk-element abundances in urban areas and industrial complexes may reflect the mixed contributions of natural and anthropogenic sources. Together with the predominant abundance of n-alkanes and polycyclic aromatic hydrocarbons at both boundaries, specific indices derived from their abundance may be indicative of mixed contributions from terrestrial plants, petroleum, and combustion deposited through various pathways (e.

Utilizing fluorescence indicators to apportion organic sources in estuarine/coastal sediments: A comparison with a stable isotopic model.

Coastal sediments accumulate organic matter (OM) from diverse sources, including local anthropogenic pollution. Effective source tracking of sediment OM is crucial for pollution source management. This study compares fluorescence proxies and stable isotopic ratios as tracers for sediment OM in Gangu Port, Korea.

Stable Isotope Analysis of Residual Pesticides via High Performance Liquid Chromatography and Elemental Analyzer-Isotope Ratio Mass Spectrometry.

To broaden the range of measurable pesticides for stable isotope analysis (SIA), we tested whether SIA of the anthranilic diamides cyantraniliprole (CYN) and chlorantraniliprole (CHL) can be achieved under elemental analyzer/isotope ratio mass spectrometry with compound purification in high-performance liquid chromatography (HPLC). Using this method, carbon isotope compositions were measured in pesticide residues extracted from plants (lettuce) grown indoors in potting soil that were treated with 500 mg/kg CHL and 250 mg/kg CYN and were followed up for 45 days. Our results show that the CYN and CHL standard materials did not have significant isotope differences before and after clean-up processing in HPLC.