Estuarine modification of terrestrial and riverine/estuarine organic matter may strongly affect the eventual preservation of reduced carbon in world oceans and is also important in nutrient and contaminant cycling. In this study multiple size classes of organic matter (including particles and dissolved fractions, POM and DOM) from a transect down the Delaware River/Bay system were collected and analyzed. Variations in chemical characteristics were identified using direct temperature-resolved mass spectrometry (DT-MS) and wet chemical techniques coupled with discriminant analysis and canonical correlations analysis. These comparative measures illustrate the complementary nature of traditional versus more recent mass spectrometry approaches. Within the estuary system, organic matter size class, rather than sample location, is found to be the major source of molecular-level variation. POM is enriched in proteins, nucleic acids, fatty acids, chlorophyll, and sterols, whereas DOM is enriched in aminosugar, furfural, and alkylphenol moieties. In positive ammonia chemical ionization DT-MS studies, which focus on the sugar components in POM and DOM, riverine very high molecular weight DOM (>30 kDa, <0.2 μm) is found to be enriched in deoxysugars and methylsugars compared to all other estuarine and coastal samples.
|Original language||English (US)|
|Number of pages||16|
|Journal||Geochimica et Cosmochimica Acta|
|State||Published - 2001|
Bibliographical noteFunding Information:
The authors thank J. van der Horst for assistance with DT-MS analyses, S. A. Macko for stable isotope analyses, and G. Eijkel for programming assistance and helpful discussions concerning multivariate analyses. T. I. Eglinton is thanked for initial suggestions on the methodology and statistical approaches. This work was funded by the U.S. NSF (NSF-OCE-9617892) and by the Foundation of Fundamental Research on Matter (FOM) financed by the Dutch Organization of Scientific Research (NWO).
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