Bureaucrats, emailconfirmed, Administrators
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| *[[:File:Instructions for DIY biorector.pdf]] | *[[:File:Instructions for DIY biorector.pdf]] | ||
| *[[:File:Microalgae Cultivation Workshop.pdf]] | *[[:File:Microalgae Cultivation Workshop.pdf]] | ||
| ==Experiments== | |||
| ===Experiment 1: Light impact=== | |||
| * Label the two vessels as "Light" and "Dark" using a marker or tape. | |||
| * Measure equal amounts of water (e.g., 100 ml) and pour it into each vessel. | |||
| * Add an equal volume of cyanobacteria culture (e.g., 5 ml) to each vessel, ensuring that the initial concentration is the same for both. Gently swirl the vessels to mix the water and cyanobacteria. | |||
| * Place the "Light" vessel under a bright lamp or in a sunny spot near a window, ensuring it receives consistent light exposure throughout the experiment. | |||
| * Place the "Dark" vessel in a dark area, such as a cupboard or a box, where it will not be exposed to any light. | |||
| * Observe the vessels for a period of 6-8 hours. Pay close attention to the "Light" vessel and look for tiny bubbles forming around the cyanobacteria. These bubbles are oxygen produced as a result of photosynthesis. | |||
| * Take notes on your observations, including the presence of bubbles in the "Light" vessel, and any differences in the appearance or behavior of the cyanobacteria between the two vessels. | |||
| * At the end of the observation period, compare your findings and discuss how light exposure influenced the cyanobacteria's ability to perform photosynthesis, as evidenced by the formation of oxygen bubbles. | |||
| ===Experiment 2: Building a simple bioreactor=== | |||
| * Clean glas containers | |||
| * Construct ports and making them air tight | |||
| * Add aluminum foil to protect ports after autoclaving | |||
| * Add tubing for bubbling | |||
| * Test the set-up regarding | |||
| * Bubbling | |||
| * Mixing | |||
| * Various | |||
| * Fill with destilled water | |||
| * Autoclave | |||
| ==Resources== | ==Resources== | ||