I'm back. Hope to fill in some of the missed days when I have a moment. On my trip, I was amazed at the number of people who read these pages regularly and came over to mention them. I had observed that I get only about six thousand visits a month (at least that show on the log) and assumed that only a few read this diary regularly. Seems that is not the case. so maybe I'll be inspired to stick to it a bit more than I have lately. We're also discovering that BEE-L has many more readers than just those on the mailing list. Many read via the web interface. I've been working on the curriculum for the Green Certificate program for Lakeland College and Alberta Agriculture, and I'm afraid that has drawn away a lot of my writing effort from this site. That job should be done soon, so I'll be writing here more when that is done. Joe, Oene, and I visited Biosphere II today. The experiments are done, and Columbia University is no longer affiliated, so it looks as if not much is happening. Nonetheless, the place is pretty impressive. To my mind, one of the most interesting bits of info I gleaned at the AHPA meeting is that the Carl Hayden lab has been testing 2-Heptanone as a potential bee repellent. It seems that 2-Heptanone kills varroa without affecting the bees noticeably. 2-Heptanone is a food additive (blue cheese flavour/smell ingredient) and so should be acceptable in beehives. The problem is that it is very volatile and would be "gone in 60 seconds". Therefore the ARS is working on a micro-encapsulation process to form time-release strips that can be laid on a top bar. The strips are being designed to last the duration of treatment period, but be fully consumed by the bees by the end of that time, thus eliminating the need to go back to remove anything. Several herbal products are being tested and formulated for use against AFB as well. They were testing 2-Heptanone as a bee repellent to mix with insecticides to keep bees from visiting freshly sprayed areas, when they discovered 2-Heptanone was killing varroa. The liquid protein diet is still under development at the Carl Hayden lab. It required a reformulation after the first tests, but is now stable and able to stay fresh for long periods. Hopefully this product will reach market in volume before too long. It will be marketed under the name, "MegaBee". We're hoping to see a patty formulation, too. Patties are more flexible, but beekeepers can see the potential for drum feeding bees on pollination before taking them home. Pollination runs the bees down badly, and this may help. I am told by the researcher that this feed, unlike protein feeds currently on the market, will raise the nitrogen levels in the haemolymph of bees in a manner comparable to pollen. Current commercial feeds tested have a beneficial, but temporary effect in comparison. Today : Sunny. High minus 17. / Tonight : Clear. Low minus 28.
Joe, Oene and I drove to the bee lab to see Gordy in the morning, then I drove to Phoenix and caught my plane to Reno. I was there, and at John Ascuaga’s Nugget Casino Resort Hotel in Sparks by 8 PM. Meijers decided to forgo the drive, due to the snow reports, and plan to stay longer in Tucson, then drive up to Vancouver. When I arrived at Reno, I saw little snow. I had expected to see a lot, but the runway was bare and the streets had only small swaths here and there along the route. At the casino, beekeepers were straggling in, but many of the hotel restaurants were closed, and the place seemed half-closed. Apparently, the snow storms had discouraged travellers, and the place was nearly empty. I took a room and found the place quite comfortable, but also noticed that there was no coffee in the room. Strike one. Tuesday : Sunny. Increasing cloudiness late in the day. High minus 16.
In the morning, I wasted a lot of time trying to get an Internet connection. The high speed did not work, and the phone line -- in spite of the information in the book on my desk -- was not Internet compatible. I phoned and enquired and was told that nobody in the hotel had any responsibility or knowledge about this and was passed off onto a toll-free number that connected me to Toledo, Ohio. They were no help, either. Strike two! The meeting began, and, although much of the program duplicated the AHPA material, there was a different, and larger crowd, and additional presentations as well. I skipped most of the general session in the morning and spent time in the trade show and hallways, then took in a few of the topics in the commercial and queen breeders' SIGs in the afternoon. I skipped the evening reception and spent time with friends instead. Wednesday : Periods of snow. Windy. Low minus 26. High minus 24.
Breeding Bees Resistant to Varroa -
Real World - Success outside the SMR/Russian Box” — John Keefus,
France Thursday : Sunny. Low minus 32. High minus 20.
Friday : Sunny. Low minus 28. High minus 22.
Word is, in a nutshell, that SMR bees are actually hygienic bees, but with an important difference. SMR bees perform right up there with the HYG strains in standard HYG tests, however, hygienic abilities observed in bees selected for SMR extend beyond simply detecting and removing dead brood. In addition to doing equally well as HYG in detecting and removing dead brood, SMR bees are able to detect, uncap, and remove foundress varroa mites that are laying eggs and reproducing in cells. This uncapping and removal liberates the foundress, interrupts her reproductive work, and prematurely exposes the undeveloped offspring, resulting in the death of the daughters. The foundress may then enter another cell, but, if she tries to reproduce there, the cycle repeats. Thus SMR greatly reduces mite reproduction, and mites die of old age or accidents without replacing themselves. The wrinkle is that these bees seem to be much less inclined to uncap and remove foundress mites in sealed brood that are -- for whatever reason -- not laying eggs, and in any hive with varroa, there will be a considerable percentage of mites that non-reproductive, but which are just sitting out the dance in sealed in cells with the pupae. These non-reproductive mites enter the cell, stay the duration of the capping period, then emerge with the bee. This subtle fact -- that SMR bees quickly and efficiently remove reproducing mites in brood, but ignore non-reproductive mites in sealed brood --initially escaped researchers, and obscured the strong similarity between SMR and HYG. Researchers finding and observing the varroa in the sealed brood of such colonies concluded (understandably) that the bees were causing mite non-reproduction, rather than realising that the bees had already located, uncapped and pulled out most of the reproducing foundresses, leaving only the non-reproducing mites. After all, they would pull a frame of brood, brush off the bees, then go to the lab and look at the brood and mites in cells under magnification. Sure there were a few empty cells, but there always are. They observed that a high percentage of foundress mites discovered in sealed brood were non-reproducing, and that there were fewer mites -- as a percentage of total mite load --in brood than expected. They bred for this characteristic, and actually wound up with an hygienic bee, but one with special abilities -- the ability to sniff out and eject reproducing varroa mites in sealed brood. Current work -- if I understand correctly -- seems to indicate that SMR and existing HYG cross well, and that the SMR characteristic can be transmitted relatively easily to current HYG stock, so we may see some interesting things in the near future. A name change for SMR may be in the offing as well. FWIW, preliminary DNA work _seems_ to indicate that just two genes are associated with SMR, but when asked if they are the same genes that are associated with HYG, the answer from those working hard on this problem, seems to be that no one knows yet, and that there is likely more to the whole picture it than just two genes. I might mention that Dee has been saying for a long time that Lusbys' bees remove varroa foundresses, and that this is a major mechanism in the Lusby success. I think -- correct me if I am wrong -- that she also believes that using small cells (4.9) encourages that trait. I have heard others, here and there, some with small cell and some with ordinary cells, observing varroa removal, too. This new(?) information is especially interesting for those of us who think we can breed bees by looking at natural drop boards and rejecting hives with big drops. It is not that simple. We could be rejecting the best varroa fighters, using that criterion, if they are, at that moment, combating an infestation originating outside the hive. Observations over a longer period are necessary to get an understanding. (Again, credit to Dee for that). Interesting!
Here I am sitting in SLC, waiting for my flight to YYC and home. Twelve days on the road, and I'm heading home. The weather there has been chilly -- down to minus 37, I heard, and I'm not sorry I missed it. Tucson was nice, and I got outside a lot, but Reno was cool and I only left the hotel/casino to cross to the next one for several meals. I had good and free-high speed Internet connections in both hotels in Tucson, but none in Reno. The hotel claims to have wireless high speed throughout, but the signal was low in my room. I wasted an hour or two trying to use it, then discovered that it was very high priced. I tried the phone line, but it was digital and any connections I managed were very slow and error rates were almost 100%. Oh, well. That and the lack of a coffee maker in room made the place rate pretty low fore me. And that is not considering that the airport shuttle does not start service until 4:30 AM and my plane was scheduled for 5:20. I had to take a cab.
Going through my mail, I see that I have a ballot for the Alberta Beekeepers' Commission vote. The deadline is the end of the month, and eligibility is based on date of receipt by the returning officer, not mailing date. I marked my 'X' and sent it out. Wondering how I voted? Click here. I'm digging out from under a pile of email and paper today. It may be the end of the week before I get caught up. Today : A mix of sun and cloud. Wind becoming southwest 20 km/h this morning. High 4. / Tonight : Cloudy periods. Wind southwest 20 km/h increasing to 30 gusting to 50 this evening. Low minus 9. / Normals for the period : Low minus 16. High minus 5.
Although th4e weather here has been bitterly cold while I was away - down to almost minus forty -- it has warmed now and is just above freezing. That is a huge relief for us, since such extremely cold weather makes going for a walk very unpleasant, and consumes a lot of coal. Today, I'll be working, flat out, on the curriculum. I'm past the deadline and have a few days to get it done. When I've had a few minutes in the past few days, I've been working through the past several weeks of diary entries. I still have a ways to go, but that will have to take a back seat for now and happen when I have a few personal moments. Suffering diary deprivation? Don't forget to look back to previous years - 2004 2003 2002 2001 2000 1999 - or read the Selected Topics. I spent the day writing, and mostly wresting with MS Word. I keep thinking that I can get it to do what i want, but syles and tables keep acting up. I suppose that, after a time, these things become more obvious, but simply placing an object somewhere on a page an keeping it there can be very frustrating. Meijers are back from Arizona and they came for supper. Today : A mix of sun and cloud. 30 percent chance of showers or freezing rain this morning. High 3. / Tonight : Cloudy. Low minus 3. / Normals for the period : Low minus 16. High minus 5.
Another day of curriculum editing.
Today : Fog dissipating near noon then cloudy. High 9. / Tonight : Cloudy. 30 percent chance of showers overnight. Low zero. / Normals for the period : Low minus 16. High minus 5 << Previous Page Next Page >>
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