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Gschwend%20thesis.pdf

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-70-<br />

Potential precursors for chemical oxidation to aldehydes are the<br />

unsaturated fatty acids. TWo of the most common fatty acids found in phyto-<br />

plankton are cis-9-hexadecenoic acid and cis-9-octadecenoic acid (Ackman et<br />

al., 1968; Chuecas and Riley, 1969). Oxidation by reactants such as ozone<br />

which add to the double bond would yield only heptanal and nonanal from<br />

these compounds. It is difficult to produce octanal and decanal from such<br />

reactions, given that the appropriate fatty acids are uncommon. A second<br />

mechanism which produces all the C6-C10 aldehydes is shown in figure 2-13.<br />

This mechanism does not have to be the dominant pathway of decomposition of<br />

the fatty acids, as these adds are found in l.g/kg quantities (Jeffrey, 1966;<br />

Kattner and Brockman, 1978) while the aldehydes are found at only ng/kg<br />

levels. Side products in this reaction are omega-carboxy-aldehydes which<br />

are not volatile. The 2 fatty acids mentioned above are also found at<br />

l.gs/kg in surface slicks (Kattner and Brockman, 1978), which may be the site<br />

,<br />

of (photo?) oxidation.<br />

SUMRY<br />

Individual volatile organic compounds appear at less than 40 ng/kg in<br />

open-ocean samples from diverse areas such as the Sargasso Sea, the western<br />

Equatorial Atlantic, and the Peru upwelling region. Total volatiles for<br />

the analytical window investigated range between 10 and ioa ng/kg. These<br />

low levels may indicate: (I) insignificant sources were present, (2) rapid<br />

turnover of these organic compounds occurred, or (3) degassing to the atmos-<br />

ph ere was important.<br />

Pentadecane is present in most surface seawater samples at about LO-40<br />

ng/kg, which is very near the calculated thermodynamic solubility (Schwarzenbach<br />

et al., 1978). This hydrocarbon may be produced from an abundant phytoplankton

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