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- Feb 23, 2020
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I have been at about 101What temp have you been at? My method might be a little unorthodox, but I usually wait until they pip internally before I raise humidity.
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I have been at about 101What temp have you been at? My method might be a little unorthodox, but I usually wait until they pip internally before I raise humidity.
Ah, I see. Makes sense nowI set 30 and we have 21 so far. 7 were not fertilized and the others had blood rings. I marked them all as I was candling, the ones that were doing good. That's what those marks are from. A couple others I put question marks on because I couldn't tell if I liked what I seen or not. That way I could watch and make sure they were developing and know which ones I was unsure of.
What would you do in this situationRight, and some of those air sacs do look a little on the small side to me.
Just me over thinkingAh, I see. Makes sense now![]()
I would wait until I saw an internal pip. But let's ask a couple other members what they would. @WVduckchick, @Pyxis, what would you do?What would you do in this situation
should I wait to raise the humidity until I see internal piping and give the air sac a chance to grow a bit moreWhat temp have you been at? My method might be a little unorthodox, but I usually wait until they pip internally before I raise humidity.
Just seen your comment. I appreciate you tagging others for input!I would wait until I saw an internal pip. But let's ask a couple other members what they would. @WVduckchick, @Pyxis, what would you do?
I think they are gonna be just fine. I dont see anything wrong. Keep up the good work.I just need a little piece of mind and possibly some advice. I am scared my babies air sacs are to small and we are on evening of day 17th. I took these pictures just a couple of minutes ago. Are the air sacs okay or do I need to do something quick so they don't drown on hatch day? I have them in a homemade still air incubator and I had terrible terrible luck with thermometers and hygrometers. I did all the calibration stuff with the salt and they all were within a descent range and I took note of the differences but once they all went into the incubator they are all over the place as in 5-10 degrees difference and sometimes 10-20 percent difference. What do I do?