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alancooper
02-07-2014, 09:38 AM
Using the Ben Hardin method, I recently grafted 15 larvae into cell cups. Eleven of the grafts formed good looking queen cells that were transferred to hair curler cages and kept in an incubator. Of the three queens that hatched, two died after a couple of hours and one survived. grafting was straightforward from healthy bees and incubation conditions were good. Can anyone suggest likely reasons for the failure?
Alan.

Jon
02-07-2014, 10:12 AM
A virgin queen which emerges in an incubator need to feed immediately or it will be dead in a few hours.
Put a little food in the bottom of the roller, a fondant honey mix will do.
You could also put a couple of nurse bees in the roller if she is going to be in there for a few days.
The critical period for development is the 4 days after the cell is sealed when the larva is pupating.
If there is chilling or rough handling during this period you will lose queens.
Transporting from the Cell raiser to the incubator needs to be done quickly and carefully if you move cells just after sealing.
I usually move mine to the incubator 2-3 days before emergence when the cell contents are much more resilient.
The other thing you should do is flatten the queen cell she has emerged from so she cannot go back in.
A hungry queen goes back into the cell head first looking for remnants of royal jelly and dies of starvation inside.
You should be getting 13or 14 queens emerge from 15 cells so the problem is with chilling, transport or humidity level in the incubator.
You need to make sure the water trays are kept topped up.

PS Alan. I presume you are one of the queen rearing group Willy Blakely is advising in Fermanagh.

alancooper
02-07-2014, 12:41 PM
Jon,
Yes I am part of the queen rearing group. Willie gave us excellent advice (he covered most of your points) which we have followed for the last six weeks or more but I have not recently contacted Willie. We have raised some fertile queens already but our success rate is low - we have put this down to our "learning process". From the grafting to the emergence stage our success rate has been around the 20-50% mark. Your advice has highlighted "transport" as a possible cause (your other points are OK) - ie., we have been taking our incubator home from the apiary by car (20-40 min or more of careful driving). We will now probably leave the incubator in the apiary to test if transport might be the cause.
Thanks for your advice.
Alan.

Jon
02-07-2014, 01:27 PM
Why not leave the cells to day 10 from grafting before moving them?
Hi Alan
The queens are fully formed at that stage and will not be harmed by jolting or chilling unless it is excessive.
I move cells from colony all the time at this stage. I put the rollers on them and put them in my rucksack and cycle home from the apiary.
An hour out of the colony does them little or no harm at this point.
Humidity in the incubator is also important. If the humidity is too low the cell wall dries out and the queens fail to emerge.

Willy B will keep you straight. I work with him a lot through the NIHBS stuff.

alancooper
03-07-2014, 09:09 AM
Jon,
Last night we opened the unhatched queen cells. Most had dead, late-stage (dark) but small Qs inside. Some cell lids showed signs of chewing. We speculated that that there not been enough royal jelly - and will be grafting again.
Say hello to Willie for me.
Alan.

Jon
03-07-2014, 08:00 PM
You sure the humidity level in the incubator is high enough?

fatshark
03-07-2014, 09:31 PM
I have no means to measure the humidity but suspect it would be difficult - particularly in a homemade Heath-Robinson setup like I use - to make it too high. I have an ice cream container containing a litre or so of water adjacent to the caged cells and usually get an acceptable proportion emerging. However, I have less success with introducing (or keeping alive*) virgins, so prefer to use them as cells.

* and pretty much abject failure keeping virgins alive, caged, in a queenless colony.

alancooper
04-07-2014, 06:40 AM
You sure the humidity level in the incubator is high enough?

Jon,
Yes - water was always in the bottom of the incubator (a new one) and the electronics gave high humidity and optimum temp readings. Plus a small amount of honey in the bottom of the curler cage.
Thanks for you comments.
Alan

Jon
04-07-2014, 10:56 AM
fatshark, the virgins seem to be fine in a roller cage in the incubator for a few days as long as they have food.
Even better if you put in a few attendants.

Jon
04-07-2014, 10:59 AM
Alan, are you using the Brinsea Octagon Incubator? Most of the queen rearers have that one.
I have one of those and have been getting good emergence rates but I always move the cells to the incubator late on in development.

alancooper
05-07-2014, 08:58 AM
Alan, are you using the Brinsea Octagon Incubator?

Jon,
It is a Brinsea incubator. In our apiary, we put grafts into a cell raiser colony (Wed evenings), then a week later transfer sealed cells to curler cages (with a drop of honey in the bottom) which are put into the incubator and taken home by one of us. Hatching is usually the following Monday. The Qs stay in the incubator until Wed evening, then they are transferred to Apideas in our apiary. Maybe with time our success rate will improve.
Alan.

Jon
05-07-2014, 08:31 PM
If you transfer the cells to the incubator after ten days rather than a week you will get a far better emergence rate. I try and put the cells into the apideas on day 11, ie 24 hours before expected emergence of the queen. Moving cells between day 5 (when cell is sealed) and day 9 from grafting has to be done really carefully as this in when pupation is taking place.
There is no advantage gained by moving cells early to the incubator.

alancooper
06-07-2014, 08:05 AM
Jon,
We work on a weekly schedule because we are a group and find the routine convenient. I take your point about cells moving to the incubator at a late development stage - thanks.
Alan.

prakel
06-07-2014, 09:06 AM
Apologies for trying to hijack this thread but...

I've been thinking of getting an incubator for some time now but have held off due to an inability (so far) to justify it financially -our bees are on a very tight budget. What strikes me, the more I read from different sources, is the very small amount of time which people keep cells in the machine for. What I'm wondering is whether those of you with experience would buy one again if you were starting over.

madasafish
06-07-2014, 02:12 PM
Apologies for trying to hijack this thread but...

I've been thinking of getting an incubator for some time now but have held off due to an inability (so far) to justify it financially -our bees are on a very tight budget. What strikes me, the more I read from different sources, is the very small amount of time which people keep cells in the machine for. What I'm wondering is whether those of you with experience would buy one again if you were starting over.

I made my own: a cardboard box. insulation and a heated floor thermostat switching on/off a (sprayed red) 25 watt lamp.. Cost (the thermostat on ebay) £15.

Hatched turkey eggs, quail eggs and bee queens.. Manual egg turning for birds.. Could not justify buying one.

But now I use cell protectors and don't use it...

My meanness has nothing to do with being brought up in Banffshire and being a student in Aberdeen. Err...

fatshark
06-07-2014, 07:33 PM
I use my honey warming cabinet … it has accurate temperature control. I increase the humidity with a pan of water. Works fine, though I prefer to use cells rather than emerged virgins.

greengumbo
08-07-2014, 09:43 AM
I use my honey warming cabinet … it has accurate temperature control. I increase the humidity with a pan of water. Works fine, though I prefer to use cells rather than emerged virgins.

Do you go for a specific humidity fatshark ? At work we use different saturated salt solutions to control the humidity.

fatshark
08-07-2014, 06:44 PM
Nope … I simply have a litre or so of water adjacent to the cells. Low tech, that's me ;)

Beefever
09-07-2014, 07:55 AM
Why bother complicating things with an incubator? I don’t raise continuous batches of virgin queens (or cells) for introduction but if I did, I’d cage the cells and rear the next batch a few frames away. Is that plausible?

Jon
09-07-2014, 02:05 PM
I got an incubator for the first time this year and am finding it really useful.
I move the cells to it about 3 days before emergence and transfer them to apideas a day before emergence.
You can hold the cell up to the light to see if it has a viable queen in it.
You can also usually see if it is a runt or normal size.
One advantage is that you have the cells at hand when you need them and don't have to go rooting through a colony to get them out in ones and twos.
Having said that, I reared loads of queens without the use of an incubator this past 4 or 5 years.