Martin G
New Bee
- Joined
- Apr 16, 2012
- Messages
- 75
- Reaction score
- 0
- Location
- Wales
- Hive Type
- National
- Number of Hives
- 6
Yesterdays inspection revealed a supersedure cell (90% sure) It’s got royal jelly but I couldn’t quite see how developed the lave/egg was. There were a couple of other empty cups but nothing which seemed well developed.
The existing queen seems to be laying fine with good brood pattern, so the plan is to use the supersedure cell to make increase. Then if the queen does fail in a few weeks time I will, hopefully be in a position to replace her.
The last inspection before this was only 2 days previous when I originally saw the cell with nothing in it, hence rechecking yesterday, so I assume there is an egg in the cell, with that in mind do the nurse bees start filling the cell with royal jelly before the egg hatches? I suppose on the first inspection there could have been an egg which I missed.
I thought of taking the frame with the cell on, once it’s sealed, with a mix of capped/uncapped brood and some stores and moving them to a nuc.
Alternative was to move the existing queen with the mix of frames to the nuc and leave the supersedure cell in the existing hive.
Any ideas on which would work best.
I estimate that the cell should be capped at the earliest in 3 days alternatively 4
The existing queen seems to be laying fine with good brood pattern, so the plan is to use the supersedure cell to make increase. Then if the queen does fail in a few weeks time I will, hopefully be in a position to replace her.
The last inspection before this was only 2 days previous when I originally saw the cell with nothing in it, hence rechecking yesterday, so I assume there is an egg in the cell, with that in mind do the nurse bees start filling the cell with royal jelly before the egg hatches? I suppose on the first inspection there could have been an egg which I missed.
I thought of taking the frame with the cell on, once it’s sealed, with a mix of capped/uncapped brood and some stores and moving them to a nuc.
Alternative was to move the existing queen with the mix of frames to the nuc and leave the supersedure cell in the existing hive.
Any ideas on which would work best.
I estimate that the cell should be capped at the earliest in 3 days alternatively 4