I prefer to call it magic, but whatever.Got it, witchcraft!
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I prefer to call it magic, but whatever.Got it, witchcraft!
No, the second chart is the same information shown in the first, but in 10nm bandwidths. You astutely see where I'm headed with this - I'm preparing an Excel chart on wavelength/Seneye PUR for comparative purposes.I'm assuming absorbency also rolls off gradually below 400nm rather than straight to nothing?
Edit: I guess that is what the first image shows vs what the Seneye can read?
Hey there in Duluth Georgia. I shipped the fluorescent lamps and fixtures but haven't gotten around to unpacking them yet. So many lights, so little time.Hey Dana, any plan to add T5 to the tests? Maybe just with the common ATI Blue+
Yes. I've got a chlorophyll chart showing UV absorption. Somewhere. It trails off gradually more or less.I'm assuming absorbency also rolls off gradually below 400nm rather than straight to nothing?
Edit: I guess that is what the first image shows vs what the Seneye can read?
Hey there in Duluth Georgia. I shipped the fluorescent lamps and fixtures but haven't gotten around to unpacking them yet. So many lights, so little time.
Yes, of course. Excuse my poor memory. I've got MACNA and the Europe presentations behind me. PM me about ARC.Yea Duluth vs Dallas. So close yet so far... in Atl traffic.
I'm Adam for ARC. We meet at Shac's a couple years ago and had a few emails back and forth...
Here you go. From Shirley Jeffrey's works. I discussed things with her from time to time, and was saddened when she passed away. She did some cutting edge work, but male peers would not let her indicate she was female (by using her first name.) Instead, she had to publish as S. Jeffrey. OK, got that off my chest.I'm assuming absorbency also rolls off gradually below 400nm rather than straight to nothing?
Edit: I guess that is what the first image shows vs what the Seneye can read?
I failed to note that absorbance was calculated using a polished Porites skeleton as the reference (instead of a Lambertian surface such as commercially available products.) Hence, we're seeing the true absorbance of corals tissue and zooxanthellae. This coral displayed zero fluorescence so that would not affect the result. I almost sold the PAM fluorometer using a red LED as the actinic source, glad I didn't as it is one of the few ways to examine absorbance without the interference of fluorescence. Sorry.I wasnt able to see the images until I quoted you for some reason.
In case anyone else had the same issue:
What candles did you use, and what are their PAR readings?Same here, and I've been around reefing since we used candles to grow sps. Kids these days wouldn't believe it ! ;-)