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Salinity Intrusion and Seasonal Water Quality Variations in the Tidal ...

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ocearnc ongm, But Phosphate level recovers from <strong>the</strong> <strong>in</strong>itial slump <strong>and</strong> rises <strong>in</strong> l<strong>in</strong>e<br />

with chloride <strong>and</strong> peaks along with chloride, <strong>and</strong> <strong>the</strong>n curiously enough, falls <strong>in</strong> phase<br />

with chloride. Phosphate level rises because <strong>the</strong> sewage <strong>in</strong>put is not flushed out as<br />

residual flow becomes too weak to take care of <strong>the</strong> nutrient load. Anoxic or near<br />

anoxic conditions prevail<strong>in</strong>g dur<strong>in</strong>g <strong>the</strong> dry months corroborate this fact. But P<br />

should fall when Cl rises. It does not happen so because <strong>the</strong> expected nse In<br />

alkal<strong>in</strong>ity <strong>and</strong> pH does not happen <strong>and</strong> also because of <strong>the</strong> accumulation of sewage.<br />

Thus phosphate rema<strong>in</strong>s <strong>in</strong> suspension all along <strong>the</strong> dry months. The reason why<br />

alkal<strong>in</strong>ity does not rise with <strong>the</strong> <strong>in</strong>trusion of cations is to be expla<strong>in</strong>ed <strong>in</strong> terms of<br />

carbonate-bicarbonate balance.<br />

The govern<strong>in</strong>g equation is CO2+H 20 H2CO 3 H+ +HC03<br />

When H+ ions are added to <strong>the</strong> system bicarbonates <strong>and</strong> protons are consumed to keep<br />

<strong>the</strong> proton concentration constant produc<strong>in</strong>g H 2C03. When OH ions are added to <strong>the</strong><br />

system, H+ ions are consumed form<strong>in</strong>g water more H+ ions are produced by <strong>the</strong><br />

dissociation of carbonic acid to form protons <strong>and</strong> bicarbonate. Insoluble calcium<br />

carbonate molecules play a crucial role <strong>in</strong> this reversible buffer<strong>in</strong>g reaction.<br />

But it is to be assumed that <strong>in</strong>trusion of mar<strong>in</strong>e cations does not reach<br />

significant levels to <strong>in</strong>itiate a perceptible change <strong>in</strong> <strong>the</strong> local aquatic chemistry. It is<br />

<strong>in</strong>terest<strong>in</strong>g that total hardness <strong>and</strong> sulfate ephemerally fall sharply <strong>in</strong> February after<br />

<strong>the</strong> <strong>in</strong>itial rise, which co<strong>in</strong>cides with <strong>the</strong> fall <strong>in</strong> phosphate; <strong>and</strong> alkal<strong>in</strong>ity temporarily<br />

rises at this stage. The plant nutrients N03-N <strong>and</strong> P04 -P are never above <strong>the</strong><br />

dangerous levels <strong>in</strong> <strong>the</strong> water bodies. Total iron, for one, is <strong>in</strong> most cases above <strong>the</strong><br />

recommended levels. But iron is not a grave aquatic pollutant; it is more of an<br />

87

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