Biomedical subjects

Yaorong Qian

Publications and source records attributed to Yaorong Qian.

4 recordsLinked to original sources

PubMed2006

Sorption of organic pollutants by marine sediments: implication for the role of particulate organic matter.

The objective of this study was to quantify sorption properties for kerogen/black carbon (BC)-bearing sediments. Single-solute sorption isotherms were measured for five pristine marine sediments using phenanthrene, naphthalene, 1,3,5-trichlorobenzene, and 1,4-dichlorobenzene as the sorbates. The results showed that the sorption isotherms were nonlinear and that the organic carbon normalized single point K(OC) values were comparable to those reported in the literature for the purified kerogen and BC, but are much higher than the data reported for HA and kerogen/BC-containing terrestrial soils and sediments. It is likely that kerogen and BC associated with these pristine marine sediments may not be encapsulated with humic acids or Fe and Mn oxides and hydroxides as often do in terrestrial soils and sediments. As a result, they may be fully accessible to sorbing molecules, exhibiting higher sorption capacities. The study suggests that competition from background HOCs and reduced accessibility when kerogen and BC are associated with terrestrial sediments may dramatically increase variability of sorption reactivities of geosorbents. Such variability may lead to large uncertainties in the prediction of sorption from the contents of kerogen and/or BC along with TOC.

Geologic Sediments↗

PubMed2006

Molecular and stable carbon isotopic characterization of PAH contaminants at McMurdo Station, Antarctica.

The molecular and stable carbon isotopic compositions of contaminant polycyclic aromatic hydrocarbons (PAHs) at McMurdo Station, Antarctica were analyzed in samples collected from land and sub-tidal area. PAHs in the study areas were characterized by high amounts of naphthalene and alkylated naphthalenes from petroleum products introduced by human activities in the area. Principal component analysis (PCA) of PAH composition data identified multiple sources of PAH contamination in the study area. Compositional assignments of origins were confirmed using compound specific stable carbon isotopic analysis.

Antarctic Regions↗

PubMed2005

Polycyclic aromatic hydrocarbon purification procedures for compound specific isotope analysis.

Purification and isotope analysis methods were developed to accurately measure the stable carbon isotope ratio of individual PAHs in environmental samples. Sample extracts were separated into several fractions by column chromatography and were purified by high-performance liquid chromatographic and thin-layer chromatographic techniques. The mean recovery of the purification method for all compounds was approximately 80%. The purity of isolates was verified by GC/MS in the full scan mode. The accuracy and precision of the method were verified using authentic standards of known isotopic compositions. The standard deviation for multiple analyses ranged between 0.1 and 0.4%o for standard material and between 0.1 and 0.7%o for environmental extracts after purification. The purification and isotope analysis methods were used to discern the sources of PAHs in environmental samples using variations in stable carbon isotopic compositions of individual compounds. Itwas confirmed thatthe purification method effectively purifies environmental samples while retaining original isotopic signatures so that PAH content and stable isotopic compositions can be used to infer contaminant sources in complex environmental settings.

Carbon Isotopes↗

PubMed2004

Degradation of picric acid and 2,6-DNT in marine sediments and waters: the role of microbial activity and ultra-violet exposure.

Bio- and photo-transformation of two munitions and explosives of concern, 2,6-dinitrotoluene (2,6-DNT) and 2,4,6-trinitrophenol (picric acid) were assessed in spiked marine sediments and water. A sandy and a fine-grained sediment, with 0.25% and 1.1% total organic carbon, respectively, were used for biotransformation assessments at 10 and 20 degrees C. Sterilized sediments were used as controls for biotic vs. abiotic transformation. Transformation products were analyzed by HPLC, GC/MS and LC/MS. Biotransformation in sediments started soon after the initial contact of the chemicals with the sediments and proceeded for several months, with rates in the following sequence: fine-grain at 20 degrees C > fine-grain at 10 degrees C > sand at 20 degrees C > sand at 10 degrees C. The biotransformation paths seemed to be similar for all conditions. The major biotransformation product of 2,6-DNT was 2-amino-6-nitrotoluene (2-A-6-NT). 2-Nitrotoluene (2-NT) and other minor components, including N,N-dimethyl-3-nitroaniline, benzene nitrile, methylamino-2-nitrosophenol and diaminophenol, were also identified. After more prolonged incubation these chemicals were replaced by high molecular weight polymers. Several breakdown products of picric acid were identified by GC/MS, including 2,4-dinitrophenol, amino dinitrophenols, 3,4-diamino phenol, amino nitrophenol and nitro diaminophenol. Photo-transformation of 2,6-DNT and picric acid in seawater was assessed under simulated solar radiation (SSR). No significant photolysis of picric acid in seawater was observed for up to 47 days, but photo-transformation of 2,6-DNT began soon after the initial exposure to SSR, with 89% being photo-transformed in 24 h and none remaining after 72 h. High molecular weight chemicals were generated, with mass spectra ranging from molecular weight 200-500 compared to 182 for DNT, and the color of the stock solution changed from clear to orange. Complexity of the mass spectra and mass differences among fragments suggest that multiple polymers were produced and were co-eluting during the LC/MS analyses.

Bacteria↗