gill_za
Never Knows Best
Hello,
I have recently came into possession of some cephalotus seeds and after searching on the forum, came up with a plan to sow them. Some one else on this forum used seed-starter sponge to propogate pullings, maybe RSS or Jcal, can't remember. But I got inspiration for this from them.
Some time ago I saved the styrofoam vial holders motivated by some vague idea of their usefulness in the future. The holders are about 1.25" deep and have cavities which are 5/8" in diameter and about 1" deep.
The plan was to have them sit in a tray with water so after experimenting with the diameter of the drain, each was stuffed with washed and trichoderma inoculated LFS.
Each cavity would hold 1 seed placed directly in the middle (or as close as possible). Each seed packet contained 3-4 seeds, so I filled three rows and left the ones in between empty.
I poured some flowable trichoderma solution onto each cavity as well, stuffed the whole thing into a ziploc bag and placed onto my southwest facing window. After reading the threads here and on other forums it looked like the stratification was not a guarantee to success so these were not stuffed into a refrigerator.
The tray might not be getting enough light so I might put it under fluorescent lights instead.
Questions? Comments? Suggestions?
I have recently came into possession of some cephalotus seeds and after searching on the forum, came up with a plan to sow them. Some one else on this forum used seed-starter sponge to propogate pullings, maybe RSS or Jcal, can't remember. But I got inspiration for this from them.
Some time ago I saved the styrofoam vial holders motivated by some vague idea of their usefulness in the future. The holders are about 1.25" deep and have cavities which are 5/8" in diameter and about 1" deep.
The plan was to have them sit in a tray with water so after experimenting with the diameter of the drain, each was stuffed with washed and trichoderma inoculated LFS.
Each cavity would hold 1 seed placed directly in the middle (or as close as possible). Each seed packet contained 3-4 seeds, so I filled three rows and left the ones in between empty.
I poured some flowable trichoderma solution onto each cavity as well, stuffed the whole thing into a ziploc bag and placed onto my southwest facing window. After reading the threads here and on other forums it looked like the stratification was not a guarantee to success so these were not stuffed into a refrigerator.
The tray might not be getting enough light so I might put it under fluorescent lights instead.
Questions? Comments? Suggestions?
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I bring home all the trash from the lab I think might be slightly useful. I am a hoarder.
