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“I chose LSSU expecting a very good engineering education. What I didn’t expect was faculty with real-world engineering experience and abilities, labs with real-world equipment, projects with real-world outcomes, and an entire campus staff with real interest in my success, as a student and yet today. My LSSU engineering education has created or supported every desired career opportunity. LSSU was absolutely the right place for me.”

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Mechanical Engineering 1999,
Vehicle Test & Development,
Electronic Brake Systems Group

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Learn more about our Engineering Living Learning Community by contacting Dr. Joseph Moening.
Engineering House 2015-2016
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Incoming Student Deadline: April 10, 2015
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Investigat- ing the Use of QPCR: An Early Detection Method for Toxic Cyano- bacterial Bloom

Garrett Aderman

Harmful algal blooms (HABs), including cyanobacterial harmful algal blooms (CHABs), are a global phenomenon. In the US, annual economic loss due to HABs was recently estimated at $82 million. Furthermore, the consensus amongst the scientific community is that the frequency and duration of CHABs in freshwater systems will increase as a result of climate change and anthropogenic nutrient enrichment. Due to the ability of some strains of CHAB genera to produce toxic compounds, larger and more sustained CHAB events will become an even greater threat to drinking water. Of all the known cyantoxoins, one of the most ubiquitous is microcystin (MCY). Humans are primarily exposed to cyantoxins through drinking water consumption and accidental ingestion of recreational water. The increasing risk presented by these toxins requires health officials and utilities to improve their ability to track the occurrence and relative toxicity. Current tracking methods do not distinguish between toxic and non-toxic strains. Biochemical techniques for analyzing the toxins are showing considerable potential as they are relatively simple to run and low cost. My goal was to develop a quantitative polymerase chain reaction (qPCR) method to measure the amount of mcyE gene in a Lake Erie drinking water and compare the levels of the mcyE to toxin produced. This is the first step to determining if the presence of mcyE of the mycrocystin synthestase gene cluster in Microcystits, Planktothrix and Anabaena cells can be used as the quantitative measurement in an early detection warning system for recreational and drinking waters.

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