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-57-<br />

approaches to the study of organic matter in the sea have previously<br />

suggested the importance of this phenomenom. Menzel (1975), in his<br />

review of organic matter in the sea, has speculated that DOC is<br />

rapidly decomposed after pulse inputs since only poor correlation with<br />

measured primary productivity and DOC values could be found. Obser-<br />

vations on specific organic metabolites such as amino acids (Lee and<br />

Bada, 1975) have also led investigators to conclude that these<br />

compounds are quickly removed af ter release in to seawater. Thus, it<br />

appears that the concentrations of some biochemically labile materials<br />

may be controlled in seawater by heterotrophic activity.<br />

Volatile compounds, whose principal source is production in<br />

surface seawater, have an additional sink from seawater in transport<br />

into the atmosphere. The mixed layer of the open ocean is degassed<br />

with a residence time of about i month (Broecker and Peng, 1974).<br />

Therefore, unless sources in the mixed layer continually produce a<br />

volatile organic compound, this atmospheric sink will rapidly deplete<br />

the individual volatile organic compound concentrations to values in<br />

equilibrium with the atmosphere.<br />

The total volatile fraction found in the Sargasso Sea and the<br />

Peru upwelling region samples comprises less than O. OL% of the DOC.<br />

Specific Volatiles: ,Pentadecane<br />

Pentadecane was the best-studied volatile compound. It was<br />

ubiquitous in surface seawater samples at a concentration near its<br />

calculated thermodynamic<br />

solubility (Schwarzenbach et aL., 1978).<br />

The lack of other homologues (e. g., tetradecane and hexadecane)<br />

indicates that this compound was not derived from a fossil fuel<br />

source. Land derived dust, for example, from the region of the

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