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Gschwend%20thesis.pdf

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-103-<br />

These data suggest the source of these alkylated benzenes may be related<br />

to the activities of tourists and summer residents on Cape Cod. A plot<br />

of the o-xylene data according to the day of the week in which the<br />

samples were taken clearly shows higher levels earlier in the week<br />

(figure 3-11). Separating the summer data from those of the "off season"<br />

further emphasizes this trend in the summer. Thus one may reasonably<br />

hypothesize that gasoline use by automobiles or motorboats has introduced<br />

these pollutant hydrocarbons into coastal seawater, especially during<br />

periods of intense tourism. Levels climb to about 3 times those seen<br />

during the rest of the year. Based on the plot of o-xylene concentration<br />

versus day of the week, it appears that this anthropogenic input is<br />

removed from the coastal seawater with a halflife of about l-2 days.<br />

This is consistent with the observed decline of the o-xylene levels after<br />

the Memorial Day weekend, 1978. A combination of air-sea exchange and<br />

tidal flushing may be sufficient to lower the o-xylene levels this quickly.<br />

It is also apparent from this information that the time scale of interest<br />

for these volatiles is on the order of days and not weeks.<br />

Ethyl benzene concentrations do not always appear to covary with<br />

the other alkylated benzene isomers because ethyl benzene was unresolved from<br />

another compound in the chromatograms. CI-CH4 mass spectral examination<br />

of this mixed peak in a sample acquired in February, 1978 revealed the<br />

simultaneous presence of a compound of molecular weight I08 (figure 3-12).<br />

This molecular weight assignment is assured due to presence of M + l, M<br />

+ 29, and M + 41 peaks in the CI-CH4 spectrum. The m/ e 95 fragment<br />

suggests that the compound contains a terminal ethenyl group (Field, 1968),<br />

while the m/ e 93 fragment indicates the presence of a terminal. methyl<br />

substituent. It is known that the brown alga~ Fucus spp.~ utilizes<br />

-<br />

trans, cis-l,3,5-octatriene (mw 108) as its sexual chemotactic agent

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