Yay fast-growing plants, floating and emergent espec. ! Tell me what shipping would be and if you PayPal and let's private message final arrangements.
Plants are so important in the freshwater DSB scheme I employ. They absorb all kinds of metals, including non-nutritive ones like lead, and not only eat up nitrates but many species preferentially absorb NH3, as I understand it because it crosses cell membranes very easily (NH4 is actually positively charged and repelled by cell membranes). Or perhaps it is just NHx, either 3 or 4, that is taken up easily. Nitrite is also somewhat preferentially absorbed by many species of aquatic plants. If you have good growth, you remove the nitrogenous waste that isn't liberated by denitrification simply by trimming your plants! Along with it go a bunch of toxic (as well as nutritive, nontoxic) metals.
Oh, the little aquariums! My picotopes!
Well, I must say I am learning a lot but am still sorting out useful conclusions from useless and even completely counterproductive ones. I am very excited to start the next batch of picos but must wait until I've got the first batch all cycled.
I have three, I call trapezoid, cylinder, and sphereoid. Can you guess how they got their names? Har har har! Ever the creative one am I. Anyhow, trapezoid cycled completely but has the most crap dumped in it. I even squeezed out the gunk from one of my Hagen Elites (wow do I love those li'l filters!). I wonder if it was the Elite's bacteria that got in there and got 'er done. Sphereoid stalled at zero nitrites and about 0.5ppm NHx. Cylinder at 0.25ppm NHx and nonzero nitrite (but barely, much closer to 0 than to 0.25 using the API test kit).
So, I put an Elite filter in cylinder for a while and put cylinder back under the lamp and I simply sunk sphereoid in the 10gal aquarium. The 10 gal has still been returning to equilibrium since that unfortunate misapplication of that algaecide which I realize now had been sitting around for over 20 years unused before I stupidly poured it into my little aquatic paradise. I figure that it and spereoid will find equilibrium together and sphereoid benefits from the temperature control, steady at 78F, of 10gal, and can cycle faster that way. Cylinder is, of course, an exploration of the hypothesis that some bug in the filter crud may be enough to cycle a pico.
Is it possible that the next generation may be boosted by a combination of my special sewage injections into the substrate and a generous dose of filter foam squeezin's?.
My plan is to start six picos of about 2-3 quarts' volume with 4" of that coarse-meshed sand (more than the usual 3" because it's so open I'm concerned an actually anoxic zone may not form without greater depth) and to use my sewage squirter to boost the sand in four, one to receive filter squeezin's and go under the lamp, one to get squeezin's and allow them to sink in a few days before submerging in a larger tank, one to be submerged without squeezin's, and one to go under the lamp without squeezins. Oh, and the other two will be un-supplemented with one going under the lamp and one in the tank. Oh, and there have to be two more - with squeezin's but no sewage, one to submerge and one under the lamp. Fortunately I have a five, a "five" which seems to be seven, and a ten (which doesn't seem to actually hold ten gallons), so each tank will hold a single pico and I can set them all to the same temperature.
I currently keep a log of each of my aquariums including the picos. I will try to discipline myself to be more consistent in terms of frequency of entries and detail of data.
The frameless "five gallon" tank I keep cycled very quickly and has the best water quality and least algae of all my aquariums, ever I think. I put about 4" coarse sand in it and fed it a couple of pinches of fish food about 3x week, plus I injected my anaerobically digested muck concoction one or two times a week. I started it about a month after the five gallon framed tank and the 10gal, and every few days put one of the Elites in it for a few hours. It cycled in under four weeks (at room temperature in an unheated San Francisco dwelling, which means around 65F to 70F) while the heated tanks still showed nitrites.
Like the picos, the frameless' nitrite level peaked and began falling prior to the ammonia level's peaking and falling. I notice that in common with trapezoid, it was exposed to one of the Elites.
So, I've tried injecting my gunk into the sand (all the way at the bottom) of the 5gal framed and the 10gal. I've been unsurprised to see the NO2 drop rapidly. I've notice that too much of it near rooted plants induces some blackening and rot typical of overwhelming levels of H2S. However it has to be a LOT of my magic sewage gunk and in a shallower (~3 inch deep) region of the sand. NHx levels continued to drop and were zero rapidly though nowhere near as rapidly as NO2 was. Now, ever since the great algaecide poisoning of twenty eleven, the NHx has been nonzero in those tanks though only once reaching nearly 0.5ppm and generally hanging out at or just below 0.25ppm. (I just keep the pH at 6.6 and moved out all the delicate fish and the shrimps to the frameless).
I got ahold of a 10x/60x/200x webcam microscope made by Intel as a toy, called the QX3, and I'm working on getting software together to use it. If I had Mac OS X, there is a great program to use it and if I had Windows XP there is also a program for it. But I use Linux and must do a successful build of the source code I found in order to produce an executable for my particular machine (emachines D620) and my particular Linux flavor which is the marvelous Jolicloud adaptation of the Ubuntu distribution.
Sadly, my skills with such marvelous and quirky computer operating systems, C programming, and suchlike lags far behind my linguistic and aquaristic skills. In short, I can't make the **** thing work! However, I can run Mac OS X and Windows XP in separate windows, like little computers within my real computer, if I only can get ahold of an XP Pro product key or purchase an OS X disk.
Important thing is, I'm gonna eventually get a look at and take digital pictures and even movies of whatever you can see in the substrate and filter material at 200x magnification.
Anyone able to tell me about where to get microscope slides, contrast stains, or getting software to work for me (or getting XP pro or Mac OS going?)? I promise I'll post what I find!