OK, thanks. 

Lights
Each ATS unit was operated under its own set of two 400W metal halide lights. For all trials, the height of the lights above the ATS bed (typically around 50 cm) was adjusted to yield a light intensity of approximately equivalent intensity at the center of the ATS bed. Incident light averaged 390 (range 240–633) μmol photons m-2 s-1 over the entire ATS bed measured with a quantum flux meter and probe (LI-250 Light Meter and LI-190 Quantum Sensor, LI-COR Biosciences, Lincoln, Nebraska). All units were operated under nearly continuous light (23:1 h light-dark cycle) to maximize production. Water temperature was controlled and maintained within 2°C of ambient (23–26 °C) by activating cooling fans when high.
Thanks for keeping me in check![]()
ABSTRACT
The aspects relating molecular control of the biological clocks to the cellular toxicity and the generation of reactive oxygen species (ROS) in marine algae are presented here in the following topics: (i) quantification data of the major antioxidant enzyme activities, such as superoxide dismutase, catalase and ascorbate peroxidation, aiming to gain a better understanding of the oscillatory levels of oxidative modifications in algal cells, (ii) correlation is made of the biosynthesis of low molecular weight antioxidants, such as carotenoids, melatonin, reduced gluthatione, and (iii) damage to the ROS targets, such as polyunsaturated fatty acids in membranes, proteins and nucleic acids.
The effect of ROS in photosynthetic organisms is exacerbated by excessive illumination. Excessive light energy input may, for instance, increase the levels of excited molecules such as triplet chlorophyll and singlet state O2 (1g), the latter being highly electrophylic and capable of oxidizing many other molecules.
Although the endogenous circadian and exogenously driven daily rhythms of antioxidative enzyme activities and of low molecular weight antioxidants are described in different organisms, the rhythmicity of the antioxidant system in micro and macroalgae has only recently received any significant attention (Figure 1). The activity of SOD in cell- free extracts of L. polyedrum monitored at different times of the day and night was found to be three to fourfold higher during the day. This rhythm continued in cells kept in constant light, indicating that the regulation is attributable to the cellular circadian clock (Colepicolo et al., 1992). Using Western blot techniques we decribed that the extractable levels of SOD protein change in parallel with its activity (Okamoto and Colepicolo, 2001). These experiments thus show that the protein is actually synthesized and destroyed each day, as opposed to what might seem a more economical alternative to the same end, such as inhibition and activation, by phosphorylation, for example.
In summary, the regulation and induction of antioxidants takes place in response to different kinds of environmental stress, such as changes in daylight intensity, nitrate pulses and UV radiation. Levels of antioxidant enzymes and other compounds may vary over the course of a 24 h light-dark cycle. Cellular prediction, orchestrated by the biological clock, of a higher level of oxidative status and, therefore, prompt induction of antioxidant enzymes expression must be critical to control the steady-state levels of ROS, thereby preventing the ensuing oxidative/nitrosative damage. This type of defense mechanism is especially important within subcellular sites highly prone to oxidative stress such as chloroplasts and mitochondria. Consequently, the biological clock mechanisms that control the production of ROS are conceivably of importance in understanding several aspects of susceptibility and temporal cell behavior.
When algae gets more than about 20 mm thick, it creates it's own darkness (self shading), so this probably contributes to the ability to do well in 24 hour light.
I'll have to take pics tomorrow as I'm about to go to bed, have to get up for work at 5am. The size and flow are according to the revised method starting on post 3251. IIRC 14 inches by 6.5-7 inches. ~490 gph measured. Lit on one side for 12 hours, 10pm to 10am, 26 actual watts of compact fluorescent (2 13w bulbs to cover the 14" better). 5100k or 6500k, can't recall off hand. Sized for 4 cubes/day as per your recommendation, now I feed the equivalent of 2-3/day.
What kind of pics of the display tank are you looking for?
Like I said it was working great for about 3 months. Now the exact same setup, hasn't been working since month 4, which was before the bulbs should have been changed IIRC. Thanks Floyd, I'll get the pics up tomorrow afternoon.
Sounds like a lot of the growth particles let go and floated around the tank, and are slowly dying and putting nutrients into the water.
Just a full tank shot, just to give me an idea of what is in your system. It might not matter, but you never know what I might see. But letting it go that long probably allowed the lower layers to die off and everything detached. When I let a screen go past 16-18 days, when I clean it, it's pretty much all detaches and the screen starts over, partially at least. So you might be seeing this, and cleaning every 7 days is not allowing it to restart. But I wanted to see pics in case there is something else.
Also your lamp temp is not ideal, you want 3000K or 2700K if you can get it, 5000K-6000K will work but is not the best spectrum for algae scrubbers.