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-189-<br />

Production of halogenated methanes was found in these incuba-<br />

t ions. All of these compounds have been previously reported from a<br />

red alga, Asparagopsis taxiformis (Moore, 1976). Halogenation in<br />

the Rhodophyta has been extensively documented (see Fenical, 1975<br />

for review), but little work has been done on other algal classes.<br />

Members of every algal class showed production of bromoform<br />

(tribromomethane). The low levels of apparent production by the<br />

vascular plant, Zostera, were quite startling, however. Epiphytic<br />

algae or attached microorganisms may have been responsible. Also<br />

Zostera may have accumulated this compound from the surrounding<br />

seawater only to release it upon stripping. These sorts of "pro-<br />

duction" mechanisms may also be operating for some of the algae ex-<br />

amined and ex?lain the prevalence of this production.<br />

An examination of the Fucus data suggests that maximum release<br />

of bromoform occurs in the middle of the summer, at a time when the<br />

algae may have been dormant (Conover, 1958). If a tribromo-2-keto-<br />

compound were present in the essential oil of this brown alga and<br />

were released during this period into the seawater, decomposition to<br />

produce bromoform would occur (Burreson et al., 1976, quoted in Moore,<br />

1977) .<br />

Lesser amounts of chlorodibromomethane were also frequently<br />

produced with bromoform; however strong production of this com-<br />

pound was confined to the brown algae samples.<br />

Release rates of 20-40 ng haloform*/gm dry weight/day suggest<br />

that standing stocks of 1-2 ng*/liter s~awater would result in coastal<br />

seawater. Such levels of bromoform were observed in the year-round<br />

*Note that these weight values underestimate the true halo<br />

due to insensitivity of an FIb<br />

form levels<br />

relative to the l-cl-nC8 internal standard.

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