Tag Archives: oxalic acid

2017 in retrospect

The end of the year is a good time to look back at the highs and lows of the season. What worked … what didn’t work … what on earth happened to our weather in June?

Early June 2017 ...

Early June 2017 …

June is an important month here in Fife. Early season colony buildup should be pretty much complete, most colonies will have had some sort of swarm control measures in late May, virgin queens may well be present in many hives, the OSR is over and colonies need to consolidate for the main summer flows.

But instead it just rained.

Rainfall in Fife was 225% the 40 year average, access to apiaries was problematic due to flooding and queens could only get out to mate if they were wearing ‘water wings‘.

Big mistake

Many colonies needed to be, or should have been fed, during June. Mine had reasonable levels of stores as I’d not taken much early season honey. I therefore chose not to feed them. In retrospect I think this was a big mistake.

Although not monitored carefully, I suspect brood rearing slowed, so reducing the colony size to effectively exploit the July/August flows. It was my worst summer honey crop in years.

Lesson one … If this happens next season I’ll continuously feed thin syrup to keep the queen laying strongly.

Doing the splits

Notwithstanding the incessant rain, swarm control – and the inevitable associated queen mating – went pretty well. I generally use splits of one form or another and most queens got out to mate, albeit a little slower than I’d have liked. If swarm control is needed for colonies in the bee shed we can’t do vertical splits (because of the way entrances are organised) and instead just take a nucleus colony away and let them rear a new queen.

Only ‘pretty well’ though because I suspect I lost a cast from a vertical split that went calamitously wrong. I’d left the queenless half far too strong and inadvertently also left multiple developing queen cells.


This wasn’t going to end well  🙁

I did manage to capture and hive another cast from the same colony, but the first virgin queen and well over half the workers were long gone.

So, lesson two (which I’ve been taught many times before 😥 ) is to be decisive when there are multiple queen cells in a split. Either knock them back appropriately (which I’ll explain next year) or split the box up into multiple nucs. Don’t dither. Don’t prevaricate and don’t – as I think I did this year – simply forget to check.

All the gear, some idea

I blatantly poached how to build foundationless frames with bamboo skewers from the internet. I claim zero originality here. It isn’t my idea. However, I’m pleased to say it was a great success. Simple wooden starter strips were also a roaring success. It’s very satisfying when you realise you don’t need to spend £1 per frame on foundation.

Nearly completed ...

Nearly completed …

I’ve used quite a few Abelo poly hives this season. They’re a strident colour – blue and yellow – but reasonably well made. Colonies checked this winter are doing well in them, with bees right up to the side walls on sub-zero days. This suggests to me that they are well insulated.

An Abelo/Swienty hybrid hive ...

An Abelo/Swienty hybrid hive …

There are some aspects of these hives I have yet to be fully convinced by; upper entrances, the crownboard, high condensation levels and a small Varroa tray. I’ll review them more fully when I’ve been using them for at least a full year.

Old invasives …

The bête noire of most beekeepers, the Varroa mite, has featured heavily throughout the year. In print, though thankfully not in my colonies. I’ve tried to emphasise the need to treat appropriately, using the right miticide at the right time. Since most approved (and even some unapproved 😉 ) miticides are all pretty effective, the timing of treatment is probably the most important point.

2016 temperature data and OA treatment ...

2016 temperature data and OA treatment …

In three recent posts I presented the importance of midwinter treatment, how to prepare the oxalic acid-containing miticide and how to administer it. These should probably be read in conjunction with an earlier article on when to treat, which I’ll come back to in a minute. Finally, as far as Varroa is concerned, I discussed potential ways to optimise the timing of the winter treatment by watching the weather. I suspect that most beekeepers treat too late in the winter.

If you have yet to treat this winter … get a move on!

… and new ones

The new invasive that got some coverage was, inevitably, the Asian hornet. Having first arrived in 2016 I think we’ll be subjected to annual incursions until it gets established here. Constant vigilance is going to be needed to help postpone what might be inevitable. Just because it is inevitable doesn’t mean we shouldn’t try and delay it’s permanent arrival.

Devon beekeepers got some first-hand experience of how vigilant you need to be to both spot and photograph Asian hornets in September. Martin Hocking has written about his experience in the Devon Beekeeper (pp172 and also in November’s Bee Craft)  which should be required reading for beekeepers, with a follow up article about his experience in December (see pp196). There’s an open meeting on the 20th of January at Harberton Parish Hall, TQ9 7SD where the threat posed by the Asian hornet – and how to mitigate it – will be discussed.

Although rarely mentioned this year, Small Hive Beetle now appears to be established in the Calabria region of Southern Italy. Data updated in late September and November indicates that positive wild colonies and sentinel nucleus colonies are still being found, indicating that attempts to eradicate the beetle have failed. Infested colony numbers are perhaps a bit lower than previous years, but since there’s no readily-available data on the level of surveillance, it’s not clear whether this shows that control is having an effect, or if people are just not looking as hard.


Posts have been made every Friday of the year, with a few additional ones when something important happened (Asian hornets or I was ‘advertising’ a Convention I was speaking at … OK, my talk wasn’t important, but the Welsh Beekeepers Convention was 😉 ).

Regular as clockwork ...

Regular as clockwork …

The Friday posts are intentional. It’s when most of us have time to read stuff. The regularity was not and, frankly, it’s a bit of a surprise I’ve achieved it. However, there it is. No promises it’ll continue like that. You can register to receive email notification of new posts in the right hand panel.

Visitor numbers to the site are markedly increased from last year. Page views per visit are down fractionally, but not significantly. It’s clear that more are finding the site as it becomes better indexed by the search engines, and as pages are referenced by other sites.

24 months on www.theapiarist.org ...

24 months on www.theapiarist.org …

My attempts at generating a presence on Facebook was an abject failure. I simply don’t have time to do anything other than automagically post updates from here on Facebook (as I do on Twitter, which I’m a bit more familiar and competent with … follow me on @The_Apiarist). Apologies if you tried to ‘Friend’ me (or whatever) on Facebook. I’ve cancelled all the email updates as I simply couldn’t keep up. Or, when I tried, I didn’t know how to! I belong to the pre-FB generation, or the one before that.

Beekeeping is international, with different problems – but many shared ones – globally. I’m grateful to the visitors from 161 different countries and the European Union 🙂 Less than 50% of the readers are from the UK, despite the UK-centric bias I inevitably exhibit (°C, colour, no mention of queen castles or slatted racks, precious little discussion of Langstroth hives etc.). Southern hemisphere beekeepers don’t even do things at the same time of the year, so many of the posts aren’t even topical for readers in Australia, New Zealand and South America. Whatever, I’m grateful people took the time to visit and read stuff.

And the winner is …

I don’t publish visitor numbers, but I do comment on the popularity of particular pages. For several years a post on my honey warming cabinet has been the most popular. It was originally posted ‘way back’ in 2014. Frankly, it was useful, but not particularly challenging or exciting.

But it’s all change this year. Aside from the homepage, the archive and blog pages, all of which people arrive at to to get the most recent posts, the honey warming cabinet post was a distant fourth in the 2017 rankings.

Above it were posts on vertical splits and making increase, feeding fondant and – particularly pleasingly and top this year – when to treat colonies with miticides against Varroa. I say particularly pleasingly as the When to treat? post is a serious article on an important subject, underpinned by scientific arguments. The timing of the late summer treatment is probably one of the most important events in influencing the health and overwintering success of the colony. This post was almost twice as popular as any other post this year which – because it originally appeared in early 2016 – suggests it is finally being widely cited and accessed by beekeepers.

When to treat?

When to treat? Finally getting read when it should be.

And what does the future offer?

Frankly, as I write this in mid-December with a streaming cold, a box of tissues and slathered in Vicks VapoRub (really, it’s not a pretty sight) I don’t know. I have two priorities at the moment; getting the new bee shed properly setup and (with my researcher hat and lab coat on)  starting studies of Chronic Bee Paralysis Virus. Both will get coverage here.

Bee Shed 2 ... the windows still need some work.

Bee Shed 2 … the windows still need some work …

In terms of the website I’m acutely aware there’s no proper indexing or rational list of articles on particular subjects, perhaps other than Varroa. I hope to bring some order to the chaos, allowing me to not repeat myself, to develop some themes more fully and to not repeat myself 😉 . I also know I have a load of unwritten stuff on queen rearing.

Winter time is also DIY time … dabbling with wood, perspex, Correx and Elastoplasts. Something will surely result from this, in addition to the blood loss and bad language.

If there are things you’d particularly like to read drop me a note. I’m interested in the science underlying beekeeping and have little patience with some of the dogma and That’s the way we’ve always done it stories. I’ve already written about the importance of training and the responsibilities of beekeepers. I’ve got some more on these areas planned as I think they’re too often ignored by beekeepers in the UK.

With Best Wishes for 2018. May your colonies be docile, your supers unliftable, your queens well-mated and your swarms (again) in my bait hives 😉

Happy New Year



If Carlsberg did vaporisers …

… they’d make the Sublimox sublimator.

I wonder how many beekeepers have one of these on their wish list for Santa?

Sublimox vaporiser

Sublimox vaporiser …

From being a bit of an imported oddity (I had to import mine from Icko Apiculture in France three years ago) they’re now becoming mainstream … over the last year or so they’ve been sold by an independent importer, then Abelo and – just this month – the ‘Big Daddy’ of UK beekeeping suppliers, E. M. Thorne (Rebecca at Thorne’s kindly asked if they could include links in their December newsletter to previous posts here on the Sublimox and vaporising Api-Bioxal).

The Sublimox is also now being discussed more widely on the online forums, with much of this discussion emphasising the price (they are expensive). Aside from this disadvantage, I think there are a number of significant advantages of this design of sublimator (vaporiser) which are worth emphasising.

The general principle of active and passive sublimators

Sublimators (vaporisers) are designed to heat oxalic acid (OA) crystals sufficiently that they sublimate i.e. go through a phase transition from a solid into a gas without an intervening liquid phase. As readers of this site should know, oxalic acid is highly effective against the Varroa mite – both by sublimation and trickling in solution, which has recently been covered in excruciating detail so won’t be elaborated on here.



Many sublimators (vaporisers) are passive. You add the OA to a pan, slide it into the hive entrance, apply a current to heat the pan, allow the OA to sublimate, withdraw the pan and start again. You usually need to cool the pan in water before addition of the next dose. This heat, rinse and repeat cycle takes time, but is very effective and the pan-type vaporisers are relatively inexpensive (£35-£100).

The Varrox vaporiser is one of the original and best known models, though there are any number of much less expensive copies sold by beekeeping suppliers and on eBay. Most require a 12V supply of some kind.

In contrast to these, the Sublimox is ‘active’, as is the US equivalent machine, the ProVap 110. In these the pan is pre-heated, the OA is ‘dropped’ into the pan in such a way that the vapour is generated in an enclosed space which it then escapes under pressure through a nozzle.

Probably the best sublimator in the world …

In terms of speed, convenience and ease of use I’d argue that the Sublimox is hard to beat.


Delivery of a single dose takes no more than 45 seconds from inserting the Sublimox nozzle into the hive. It’s appreciably faster than the pan-type passive sublimators. There’s a preliminary warming up period before use, as the machine reaches operating temperature. After that it’s simply treat, refill, treat, refill ad infinitum. The rate-limiting step is sealing the hive and refilling the small plastic ‘cartridge’ with OA.

For one person, a hive-a-minute is just about possible – if you have 10-20 closely spaced hives, sufficient entrance blocks and buy additional white plastic cartridges. But, to achieve this you’ll be rushing about like a mad thing and it’s not realistically achievable1.

But speed isn’t the major benefit.


Sublimox vaporiser

Sublimox vaporiser

It’s convenient because you can ‘squirt’ the gas through a small hole in hive. You don’t need to open the hive and so it works with any hive type or entrance. My favoured kewl floors cannot be used with a sublimator that needs to be pushed through the entrance. Instead, all my hives have a neat 6mm hole drilled through the sidewall of the floor which is usually plugged with a small foam bung or twist of grass2. Vapour quickly permeates throughout the hive, ensuring all surfaces are reached.

The only exception are the all-poly hives, such as the garishly coloured Abelo’s I’ve been using for work this season. The nozzle of the Sublimox gets hot and melts polystyrene (been there, done that 🙁 ). With poly hives I usually use a simple shallow eke with a Sublimox nozzle-sized hole in one side. In this case you do need to remove the roof and crownboard, add the eke, replace the roof (upside down), treat and then close up the hive.

Foam bung ...

Foam bung …

The alternative is to simply squirt the gas through the open entrance. This isn’t ideal as some of the gas will escape, potentially exposing the beekeeper and definitely not exposing the bees/mites. One way to avoid this loss of gas is to use a wooden block with a small hole through the middle held over the poly hive entrance.

It’s important to have a clear space into which the gas is ‘squirted’. If you don’t the OA tends to not permeate through the hive properly.

The Abelo hives have a hole in one face of the brood box. This is usually plugged. I think it’s intended as an upper entrance. I’ve yet to try poking the Sublimox nozzle through this hole to deliver the OA … this might not work as it may be too close to the frame, so impeding the spread of gas through the box. Time will tell.

Safety considerations

There’s an additional benefit of the way the Sublimox is used. Operator exposure to OA should be minimised. The gas isn’t generated until the machine is inserted and inverted and takes no more than ~45s to deliver. If the hive is sealed properly there’s very little exposure to the gas.

… but all this comes at a cost

The Sublimox is three-times the price of a Varrox vaporiserIs it worth it? That’s up to the purchaser to decide, based on the number of hives to be treated, the depth of their pockets, the perceived benefits of the speed, ease of use, convenience and safety etc.

Many will baulk at the cost. Some build their own. Others don’t bother vaporising, but solely dribble OA solution in midwinter. This is the cheapest and fastest way to treat colonies. I estimate it costs about 0.5p/hive to trickle treat if you buy OA in 25kg bags. Dribbling is probably even faster than using the Sublimox. However, dribbling is really only practical for broodless colonies – swarms and for midwinter use – and should only be done once per season. In contrast, repeated sublimation is tolerated well by colonies.

Would I buy another one?

Almost certainly.

Before you splash the cash


Generator …

Be aware … the Sublimox requires a 240V supply. One of my apiaries has mains power which is the best solution, but unlikely in the corner of a farmers field. You can use an inverter from a car battery which is fine if you can get your car close enough to the hives. Alternatively – and this is what I do – you can use a portable generator. I’ve got an 700W Impax one from Screwfix which works perfectly.

But that’s another £190  🙁

You’ll also need to periodically buy replacement sealing rings for the OA “cassette”. These wear out or perish rather fast. Icko sell them for a daft price, but they’re now available in the UK.

Single use ...

Single use …

You should also be aware that Api-Bioxal, the VMD-approved oxalic acid-containing miticide, has glucose in it which caramelises in the pan of the Sublimox (and other vaporisers) and is a bit of a nightmare to clean out properly. I’d go further and suggest that Api-Bioxal is unsuitable to use with a Sublimox. If the nozzle is blocked the gas has to escape and there could be inadvertent exposure of the operator.

Safety first

I’ve touched on safety above. However, just because OA vapour is generated for a very short and well defined time doesn’t make it safe. There are still exposure risks which must be taken seriously.

You’ll need PPE – personal protection equipment – to prevent exposure to the OA vapour when treating colonies. This includes eye protection and a suitable vapour mask. Don’t skimp on this and assume you’ll just stand downwind. If the hive is poorly sealed, swirling gusts of wind will expose you to vapour and it’s – at best – very, very unpleasant.

Entrance block

Entrance block …

Unlike passive vaporisers, the Sublimox generates a very large volume of gas immediately the OA is added. There’s no opportunity to ‘stand well back’ as the pan warms up as you can with the passive machines. You have to be holding the Sublimox to invert it and drop the OA into the pan. You’ll be bent over the hive and unable to avoid the swirling fog of acidic vapour if it escapes. To help minimise this seal the hive thoroughly. I use a full-width entrance block and tightly fitting Varroa tray. Even then, particularly on ageing cedar hives, there are all sorts of little gaps from which the OA vapour can be seen escaping.

Entrance block in use

Entrance block in use …

Finally, as if gassing yourself with an evil smelling acidic cloud of OA wasn’t enough, remember you’re using a 240V supply outside, probably on damp grass … or possibly even in the rain. Don’t get electrocuted. Make sure you use an RCD (residual current device) that’s been tested and you know works.

Take care.

Share the costs

At the time of writing the Sublimox costs over £300. Perhaps competition will force the price down a bit? When you consider that these machines are used relatively infrequently during the season it makes sense to consider purchasing them as an Association item (or with a group of friends), in the same way that some associations have extraction equipment available.

When compared to a reasonable extractor the Sublimox doesn’t seem so outrageously priced.

Of course, like an extractor, everyone needs it at about the same time of the season (at least in midwinter). However, unlike an extractor, it’s generally needed for a relatively short period, is easy to transport and easy clean after use. There should be no reason it couldn’t be shared by association members.

I appreciate that many associations don’t have shared equipment, or many beekeepers don’t belong to their local association. All I’m doing is suggesting a way in which a good quality and highly effective piece of equipment could be purchased so that many can benefit.

Whether you’ve got one of these on your list for Santa or not …

… Happy Christmas!

1 The rate-limiting step is probably having enough entrance blocks. If removed too soon you’ll lose lots of vaporised OA goodness. Leave it a good 5 minutes if at all possible, which is easily enough time to treat another 5 hives. See what I mean?

When treating a hive for the first time I’ve even drilled this hole through an occupied hive.

† Actually, this hole isn’t suitable. It opens onto the face (rather than end) of a frame, and the vapour is therefore restricting from spreading. Don’t bother.

‡ I’ve regularly treated colonies in the dark. Sometimes the only time I can get to the apiary is after work. The bees are all ‘at home’ but you can easily seal the hive up and treat them. Use a headtorch with a red bulb. Since bees can’t see red, any that escape won’t directly target your head and you can probably work safely without a veil.


If Carlsberg did … is one of the most recognisable advertising campaigns of all time. Originally created in 1973 it has achieved near-universal recognition and remains in daily use, though predominantly these days as internet memes. The opening three words of the adverts were as recognisable as the closing seven … probably the best lager in the world.

There are any number of comedic If Carlsberg did ‘advertising’ campaigns, including some from Carlsberg itself … Probably the best poster in the world, featured the distinctive swirly underscore, colour scheme and font, together with a real tap dispensing lager installed in Londons Brick Lane.

If Carlsberg did ...

If Carlsberg did …

Carlsberg revamped the advertising campaign in 2015 (the poster above was part of this), over 40 years after it was first used. You can view these adverts on the Carlsberg website.

I’ve used a variant of the If Carlsberg did … phrase previously, when describing the large Dadant smoker. It’s still a great smoker.

Weather to treat

Not Whether to treat? … to which the answer is yes. Instead, a poor pun on the choice of how I use temperature as an indication of when to treat colonies in midwinter …

Midwinter OA-based treatments

Oxalic acid-based treatments for midwinter Varroa control are most effective when colonies are broodless. This is because oxalic acid (OA) treatments only kill phoretic mites and are ineffective against mites in sealed cells. They are therefore ideal for use on swarms, packages and broodless colonies in midwinter.

These OA treatments include Api-Bioxal, the VMD-approved treatment, and unmodified oxalic acid, it’s active ingredient. The importance of midwinter treatments, the preparation of the OA solution and how to trickle treat have recently been covered. I’ve previously discussed sublimation and will do so again in a longer article in the future.

The beekeepers winter dilemma

How can you tell whether your colonies are broodless in midwinter?

On a warm, sunny, Spring afternoon this takes just a couple of minutes … remove the roof, crack off the crownboard, gently lift out the dummy board and the adjacent frame, look carefully at the mass of bees covering the top bars, aim for about the middle and gently prise apart those two frames, lift out a frame from one side of the ‘gap’ and – Hey presto – brood.

Just writing that in early December makes me hanker for much warmer days …

Memories of midseason

Memories of midseason

Actually, you can do exactly the same in midwinter. There are videos on the internet showing an experienced and (in)famous Finnish beekeeper opening his colonies at -10ºC.

I’ve opened and briefly inspected colonies at low temperatures (though not sub-zero). The bees are usually pretty torpid, reluctant to fly – or simply too cold to – and you can be in and out in just a minute or so. Bees cope pretty well with this. It undoubtedly disturbs them a bit and it breaks the propolis seal on the crownboard, but – done carefully and quickly – it’s the only foolproof way to determine whether a colony is broodless in midwinter.

But what if they’ve got brood and it’s therefore not the optimal time to treat? Do you go back and repeat the entire process in 1-2 weeks? What if it’s snowing next time, or there’s a howling gale blowing?

An alternative approach is needed.

The annual brood rearing cycle

As the colony moves from summer to autumn the egg laying rate of the queen drops. It goes on dropping, although not necessarily smoothly, as the days shorten further, the temperature drops and the sources of pollen and nectar disappear. If the queen stops laying altogether then the colony will become broodless about 21 days later.

At some point, perhaps early in the New Year, the queen starts laying again. Slowly at first, but at increasing levels as the season starts. Once foraging starts in earnest the egg laying rate increases markedly and peaks sometime in June.

The precise timing of all these changes cannot be predicted. It’s likely to be dependent on a range of factors – nectar and pollen availability, the strain of bee, day length (and whether it’s increasing or decreasing) and temperature.

Of these, temperature probably has the greatest influence.


Generalised annual brood and worker numbers ...

Generalised annual brood and worker numbers …

Here’s a quick’n’dirty graph put together with BEEHAVE showing a generalised annual cycle of total brood (blue) and adult bee (red) numbers. Under the conditions in this model the colony is broodless for ~30 days at the end if the year.


Part of the problem with being definitive about the annual brood cycle is the temperature variation with latitude. Temperate regions stretch – in Europe – from Northern Finland to Southern Spain. Bees are kept throughout this range, but obviously experience wildly different climates.

And then there’s the year to year variation.

So if you can’t predict when the colony is going to be broodless, perhaps you can observe the weather – and in particular the temperature – and make an educated guess.

Watch the weather

Over the last few years I’ve applied my midwinter treatment soon (<6 days) after the end of the first extended cold period of the season. This is generally earlier than most beekeepers, who often treat between Christmas and New Year, or early in January.

So, how do we reasonably accurately monitor the weather for a suitable time to treat?

Ho ho ho

Ho ho ho

Most of us live in centrally-heated splendour, protected from the day-to-variation of temperature by heated car seats, air conditioning, hot water bottles, Thinsulate and wood-burning stoves. Do you know what the temperature was today? Rather than trust the wildly-variable (in accuracy) national weather reports for the actual temperature near my apiaries, I instead use very much more local data from Weather Underground.

There are hundreds of ‘amateur’ weather stations across the country that upload data to wunderground.com. Most of these provide current and historic data, including temperature (max, min and average). Here’s one for Auchtermuchty in Fife (on wunderground.com) and directly from the weather station.

Once the weather cools I keep an eye on the average temperature over an extended period of a fortnight or so. If it remains low I wait a bit more … but I then treat as soon as practical after it warms up to 8-10°C or so.

The proof of the pudding

Here’s a graph of the temperature data for 2016§. As indicated on the graph, I treated colonies on the 7th of December.

2016 temperature data and OA treatment ...

2016 temperature data and OA treatment …

I didn’t open my colonies, but others opened on the same day nearby were all broodless. The 7th was chosen as it was the first warm (relatively!) day after a 19 day window in which the average temperature had barely climbed above 5°C.

These treated colonies went into the New Year with vanishingly low Varroa levels.

And again …

This year appears to be repeating a very similar pattern. We’ve had frosts most nights since the 10th of November. It started to warm up significantly in early December as storm Caroline bore down on Scotland and I treated most of my colonies on the 6th 

… by the light of a head torch, in light rain and strengthening wing at 7pm after work.

No, I didn’t open any of the hives to check if they were broodless  😉

It was over 11°C in the apiary when I treated, the barometer was plummeting and the forecast was for near-zero temperatures within 24 hours and remaining that way for another 10 days.

Some of my hives have perspex crownboards. These allow me to check both the state of the colony and if the vapour from my Sublimox has permeated to every corner of the hive. All the colonies were very loosely clustered, with a few bees even wandering out briefly onto the landing board in the dark as I bumbled around preparing things.

The Varroa trays will now be checked in a week or so to work out the mite infestation levels. In the meantime, I can start planning for the coming season knowing I’ve done the best I can to reduce virus levels in the colonies, so giving them a good start to the year.

A Hi tech solution?

Colonies rearing brood maintain a higher, and stable, broodnest temperature (32-35°C) than colonies without brood. It is therefore possible to determine whether a colony has brood by monitoring the temperature directly, rather than trying to infer it from the ambient temperature.

Brood rearing starts ...

Brood rearing starts …

Arnia make hive monitors that allow this sort of thing to be measured. It would be interesting to relate the brood temperature to the ambient temperature (described above) to determine how accurate or otherwise simply ‘watching the weather’ is. Of course … what you’d really want to do is monitor when brood rearing stops and treat soon after that.

Stop press

I treated colonies in our research apiary the following day – the 7th – with dribbled Api-Bioxal. The temperature had dropped almost 7°C since the previous evening and colonies were again beginning to cluster tightly. Under these conditions I’m never confident that the OA vapour penetrates fully, so prefer to trickle treat.

I briefly checked one strong colony in a poly hive for brood.

It was broodless, as I’d hoped  🙂

Of course, this doesn’t guarantee all the others are also broodless, but it does give me some confidence that I’d chosen the correct weather to treat.

† This article, like most on this site, discuss beekeeping issues relevant to temperate climates. It’s important to make this clear now as most of what follows is irrelevant to readers from warmer regions.

∞ Even if there is brood in midwinter, it’s going to be in pretty small amounts. The rate at which this brood emerges is going to be low. The chances of determining what’s going in the colony by ‘reading the tea leaves’ from the debris falling through the mesh floor of the hive is therefore not great. It would probably also require repeated visits to the apiary.

ß This needs qualifying … in midseason, when the temperature varies but it’s not generally cold, the nectar flow is probably the rate-limiting step for brood rearing. The June gap is regularly associated with the queen shutting up shop for a while. However, in late autumn and early winter I’m sure the plummeting temperatures is a major influence on egg laying by the queen.

‡ National … Ha! Most are only national if you live within the M25. Anywhere else and you’re usually much better off accessing some data from closer to home. It’s worth noting that the sort of ‘amateur’ weather stations I discuss do vary in data quality. For example, they’re a bit dodgy recording temperatures in full sun (they tend to over-read). However, if you find a local one, check the temperature in comparison to a thermometer in your apiary, you’ll find it’s a useful way to monitor what might be happening in the hives.

§ I don’t routinely generate these graphs – I have a life (!) – but did specifically to illustrate this post. It’s sufficient to simply monitor the average temperature.


Whether the weather be fine
Or whether the weather be not,
Whether the weather be cold
Or whether the weather be hot,
We’ll weather the weather
Whatever the weather,
Whether we like it or not.

















Trick(le) and treat

Tools of the trade

Tools of the trade

This is the third and final post on why, with what, when and how to minimise mite levels in colonies in midwinter.

In the first post I explained why midwinter mite treatment makes sense. In the second I described how oxalic acid-containing solutions should be prepared and stored.

Oxalic acid-containing” solutions includes both Api-Bioxal, the VMD approved treatment, and the unadulterated chemical. All three posts focus on trickling or dribbling – I’ve covered sublimation previously and both are essentially equally effective. Sublimation or vaporisation is currently very fashionable … but trickling is simplicity-itself and requires almost no special equipment.

In this post I’ll discuss how to administer the oxalic acid-containing solution.

For readability I’ll use the term OA solution to mean any oxalic acid-containing solution. About 50% of the readers of this site are from outside the UK; local rules may determine what you are or are not allowed to administer to your bees.

Trickling or dribbling

You’ll hear both terms used interchangeably1. The general principle is that you directly administer 5ml of a 3.2% w/v solution of oxalic acid in thin (1:1) syrup per seam of bees in the colony.

Directly‘ because you administer the OA solution to the seam of bees. You don’t count the seams and then simply pour it into the hive. You don’t spread it across the top bars. The idea is that the bees at the top of the seam get coated in the solution and that it dribbles down through the colony, being passed from bee to bee as they feed and groom and move about.

Two seams of bees

Two seams of bees …

During this process any phoretic mites will also get exposed to the oxalic acid. Since mites are readily damaged by the OA solution they fall off and gradually drop out of the bottom of the cluster. Gradually, as it takes a few days for gravity to deliver all the corpses.

You can therefore determine whether mites were present and killed by placing a Varroa tray underneath the open mesh floor of the hive. Note that this doesn’t tell you how effective the treatment has been … for that you’d need to know the mite infestation level before treatment as well.

When to treat

In many ways this is the critical decision. As described previously, maximal benefit occurs when the colony is broodless. Ideally you want an extended cold period late in the calendar year. The colony will cluster tightly and brood rearing will slow down or stop completely.

If the cold period has lasted 2-3 weeks, even better. This will mean that some or all of the brood present will have emerged. The more sealed brood present, the less effective trickling OA solution is as a means of controlling mites.

Choose a calm, cool or cold day. I usually wait for a day with temperatures between 0 and 5°C. Much warmer than that and the cluster starts to break up or the bees are more likely to fly about as the crownboard is lifted. Windy or wet days disturb the bees (at least when you prise the crownboard off), so it’s best to avoid those.

I prefer to treat before the year end, rather than after, if I can. From a few irregular midwinter peeks into the cluster I think queens start laying earlier than most beekeepers think.

It pays to be prepared …

Trickle 2 - £1

Trickle 2 – £1

… Aesop (~620-560BC) was right, though he wasn’t talking about beekeeping. Before treating your colonies there is some preparation needed. Do this properly and it’s a doddle.

Purchase a Trickle 2 container from Thorne’s. These are a measly quid each. You’ll only need one.

Practice with the Trickle 2 container (see below).

Gently warm your pre-prepared OA solution to about 25°C. If you made it up in advance and stored it at 4°C in the fridge this will take an hour or two. The easiest way is to stand the container (preferably thin-walled … I use a well-rinsed milk carton) in a basin of warm water.

Pour the pre-warmed OA solution into a well-labelled vacuum flask. You can buy these from Tesco for £2.50 with a capacity of 1 litre. The aim here is to take everything you need ready-prepared to the apiary so the treatments take the minimum time possible.

Remember that OA is toxic. Label everything carefully, make sure children can’t get near it and don’t use it again for food/drink purposes.

That’s it … you’re ready. You’ll need a hive tool, a bee suit, thin gloves (to protect you from the OA, not the bees), your vacuum flask of OA solution and the Trickle 2 bottle. By all means take your smoker, but you shouldn’t need it.

I’ve got a 5 ml (or 25 ml) syringe … won’t that do?

Yes … but no.

A Trickle 2 bottle holds 100ml of prepared OA solution. It takes two hands to fill the bottle, but only one hand to use it. That 100ml is sufficient for 20 seams of bees i.e. two completely full colonies (assuming an 11 frame National box). In midwinter the colony is unlikely to occupy 10 seams. A Trickle 2 bottle is also pretty accurate, reproducibly dispensing about 4.6-4.8ml of liquid. That’s close enough to 5ml.

In contrast, a syringe also takes two hands to fill (and refill). However, unless it’s a 5ml syringe, it’s difficult to accurately and reproducibly dispense liquid without using two hands. A 5ml syringe gives you the necessary accuracy, but needs refilling for every seam of bees. This takes time … during which the crownboard is off and the colony is getting chilled.

I’ve done both and can assure you that the Trickle 2 bottle is much better. Just buy one. It’s only £1 and it’ll last ages if one of your association members doesn’t borrow it … or doesn’t return it.

How to use a Trickle 2 bottle

  • Remove the cap and fill to the top of the lower chamber with liquid (practice with water).
  • Replace the cap.
  • Hold the bottle with your thumb and fingers on opposite sides of the lower chamber, with the external ‘pipe’ to the upper chamber next to your palm.
  • Undo the spout about a turn.
  • Gently squeeze the lower chamber. Liquid is forced up the pipe into the upper chamber. Hold it against the light to observe this.
  • Once the upper chamber is full, stop squeezing. Excess liquid drains back into the lower chamber.
  • If you are right handed turn the Trickle 2 bottle anti-clockwise2 using your wrist and gently squeeze the bottle to dispense the liquid in the upper chamber from the spout. If you’re left handed you need to turn the bottle clockwise.

And in practice

The single-handed operation for the Trickle 2 container really pays dividends when treating a colony. You can gently prize up one side of the crownboard, hold it in one hand, administer the OA solution to each seam with the other hand and gently lower the crownboard back down … all in less time than it took me to write that.

Like this:

This is a reasonably sized colony being treated in the second week of January 3 years ago. The video is 1’45” long, but the crownboard is only open for about 50 seconds. And I was chatting with Mick Smith off camera, so could have perhaps gone a bit faster if I’d concentrated … 😉

Here’s a more detailed view of treating a small colony:

33 seconds of warmed, acidic goodness to slaughter the mites and give the colony the best possible start to the upcoming season.

Cautions and considerations

Discard any OA solution that’s not been used. Warming it will have raised the HMF levels and this may be toxic for your bees. However, read footnote 3 for another way to avoid HMF buildup3.

Wash everything carefully – the Trickle 2 bottle, the vacuum flask, gloves etc. Since the OA solution was in syrup everything gets sticky and gummed up. Clean stuff up, make sure it’s labelled and not going to be used in the kitchen and put it away until next year.

Oxalic acid kills mites, but it’s also toxic for unsealed brood. This is perhaps unsurprising considering it has a pH of 1 (i.e. very acidic) and ‘naked’ larvae aren’t protected by the tough exoskeleton that adult bees have. This is another reason to treat during a broodless period in midwinter.

In summer, swarms can also be treated with trickled oxalic acid-containing solutions before they have sealed brood. If a swarm arrives in bait hive, let it settle and start drawing comb on the foundationless frames. A day or so later treat it with oxalic acid by trickling. When I’ve done this I usually wait until late afternoon or early evening, so most of the bees are in the box. The colony obviously won’t be clustered, but the principle is the same – 5ml of syrup down each seam. Easy peasy. Effective.

Swarms have a significant mite load, so it’s well worth treating them before they rear brood and give the phoretic mites somewhere to breed.

Finally, it’s often recommended that a colony is only treated once per year with oxalic acid by trickling or dribbling. I’m not sure where this advice originates, but it’s probably wise.

‘Vaping’ vs. trickling

The discussion forums are awash with recommendations to ‘vape’ the colony, rather than trickle. Vaporisation, or more correctly sublimation, is a widely used method and has been in use for two decades. It’s currently very fashionable. I’ll write a more substantial comparison sometime in the future, but the following brief notes might be of interest.

Sublimation can be done repeatedly with brood present (though there’s no peer-reviewed evidence of efficacy) and is both well-tolerated by the colony and is not toxic to unsealed brood. It requires specialised and potentially expensive equipment, both for delivery and personal protection. You can build your own vaporiser, but shouldn’t skimp on protection for the operator. With a well designed vaporiser and hive there’s no need to open the colony to administer treatment.

In contrast, trickling requires only the Trickle 2 bottle and vacuum flask described here. Personal protection is a pair of latex gloves. It should only be conducted when the colony is broodless, should probably only be conducted once and does require the hive to be opened (albeit briefly).

You’ll be told that vaporisation is faster. It isn’t. Watch the videos above. Even my Sublimox – probably the fastest ‘active’ vaporiser on the market – takes well over a minute per colony if you take into account sealing the box, moving the generator about, unsealing the hive etc.

There are reports that sublimation is more effective, but the difference is marginal, and possibly not statistically significant. There is also a report that colonies are stronger in the Spring after sublimation, though this may be due to toxicity to open brood by trickled OA solution. If the colony is broodless this shouldn’t be an issue.

I’ve used both many, many times without a problem. Across the UK I suspect more beekeepers trickle OA, rather than ‘vape’ (a word I dislike), though the vocal ones on the discussion forums currently favour vaporisation.

What’s more important than how you deliver the oxalic acid, is that you do treat. Trickling OA solution is so easy and inexpensive that there’s no reason not to … and your colonies will be much healthier for it.

Get dribbling 😉

If the beekeeper is of a certain age you’ll hear these terms used in a different context. We’re restricting discussions here to delivering OA 😉

If you are left handed you need to turn the Trickle 2 bottle clockwise. Actually, to be pedantic, if you are left handed and holding the bottle in your left hand, turn it clockwise. It’ll make sense once you try.

3 In the previous article on preparing oxalic acid solutions Calum posted a comment on preparing the OA in water and only adding and dissolving the required amount of sugar just before use. This has the advantage that there will be no HMF buildup. OA solution in water should be perfectly stable. I’ve not done it this way, but it makes sense and might be worth trying.


The title of this article is a twist on the term Trick or treat. This is not entirely inappropriate as Trick or treating is a Halloween (31st October … just a few days away) custom dating back – in various forms – centuries.

The modern usage, essentially North American, dates back to the 1920’s and refers to children in costumes going house to house threatening to play a trick unless the homeowner provides a treat, usually sweets or toys. In Britain these traditions date back to the 16th Century, both of children going house-to-house asking for food and of dressing up in costumes at Halloween.

Closer to home, ‘guising‘ – children in Scotland going from door to door in disguise asking for food, coins or chocolate  – dates back at least a century.

The term Trick or treat only entered common usage in the UK in the 1980’s.



Oxalic acid preparation

This is the second of three articles on midwinter treatment of colonies with oxalic acid to minimise Varroa levels. In a recent post I explained why a midwinter treatment was necessary, even if you’d treated three months earlier. Essentially this is because:

  • there will still be some residual Varroa, particularly if you treated in late summer rather than early autumn (and this post explains why early treatment is preferable)
  • midwinter is the time when brood levels are at a minimum, so most mites will be phoretic and readily accessible to the miticide treatment

Midwinter is the time to use oxalic acid-containing treatments. It can be delivered in a variety of ways; by sublimation (vaporisation), spraying or trickling (dribbling).

Trickling or dribbling

This post is about the preparation and storage of oxalic acid-containing solutions for trickling. Sublimation is covered elsewhere and spraying is not approved or widely used in the UK.

The process for trickling is very straightforward. You simply trickle a specific strength oxalic acid solution in thin syrup over the bees in the hive. The oxalic acid kills the mites. How isn’t entirely clear – it’s thought to corrode the mouthparts and soft tissue. It’s more than 90% effective in killing phoretic mites when used like this.

Beekeepers have used oxalic acid for years as a ‘hive cleaner’, as recommended by the BBKA and a range of other official and semi-official organisations. All that changed when Api-Bioxal was licensed for use by the Veterinary Medicines Directorate (VMD).

Oxalic acid and Api-Bioxal, the same but different

Spot the difference ...

Spot the difference …

Api-Bioxal is the VMD-approved oxalic acid-containing miticide. It is widely available, relatively inexpensive (when compared to other VMD-approved miticides) and very easy to use.

It’s very expensive when compared to oxalic acid purchased in bulk.

Both work equally well as both contain exactly the same active ingredient. Oxalic acid.

Api-Bioxal has other stuff in it (meaning the oxalic acid content is a fraction below 90% by weight) which actually makes it much less suitable for sublimation.

How much and how strong?

To trickle or dribble oxalic acid-containing solutions you’ll need to prepare it at home, store it appropriately and administer it correctly.

I’ll deal with how it is administered next time. This is all about preparation.

The how much is easy. You’ll need 5ml of oxalic acid-containing solution per seam of bees. In midwinter the colony will be reasonably well clustered and its likely there will be a maximum of only 8 or 9 seams of bees, even in a very strong colony.

Hold on … what’s a seam of bees?

Two seams of bees

Two seams of bees …

Looking down on the colony from above, a seam of bees is the row visible between the top bars of the frames.

Remember to prepare ~10% more than you think you need. You’ll inevitably spill some when using the Trickle 2 bottle to administer it to the colony. It’s not that expensive, so don’t risk running out.

And the how strong? The recommended concentration to use oxalic acid at in the UK has – for many years – been 3.2% w/v (weight per volume) in 1:1 syrup. This is less concentrated than is recommended in continental Europe (see comments below on Api-Bioxal).

My advice – as it’s the only concentration I’ve used – is to stick to 3.2%.

Listen very carefully, I shall say zis only once

A bit of basic chemistry coming up. Skip to the warning in red below and then the recipes if you want, but this explains some important things about working out how much to use.

The molecular formula of oxalic acid is C2H2O4. The molecular weight of oxalic acid is 90.03 g/mol. However, the oxalic acid you purchase – including Api-Bioxal – is the dihydrated form of oxalic acid.

Di as in two, hydrated as in water.

The molecular formula of oxalic acid dihydrate is C2H2O4.2H2O and oxalic acid dihydrate has a molecular weight of 126.07 g/mol.

Therefore the weight of oxalic acid in 1 g of oxalic acid dihydrate is 90.03/126.07 = 0.714 g.


Oxalic acid is toxic

  • The lethal dose for humans is reported to be between 15 and 30 g. It causes kidney failure due to precipitation of solid calcium oxalate.
  • Clean up spills of powder or solution immediately.
  • Take care not to inhale the powder.
  • Store in a clearly labelled container out of reach of children.
  • Wear gloves.
  • Do not use containers or utensils you use for food preparation. A carefully rinsed plastic milk bottle, very clearly labelled, is a good way to store the solution prior to use.

Recipes : oxalic acid

The standard recipe is 100 g water plus 100 g white granulated sugar. Mix well and then add 7.5 g of oxalic acid. The final volume will be 167ml i.e. sufficient to treat over 30 seams of bees, or between 3 and 4 strong colonies (including the 10% ‘just in case’).

This final concentration is 3.2% w/v oxalic acid … (7.5 * 0.714)/167 * 100 = 3.2. Check my maths.

0.01 g to 500 g

0.01 g to 500 g

If you have more colonies to treat, or have trouble weighing 7.5g, scale everything up ten-fold. Or buy a small, accurate set of digital scales – like these for £9 which work very well. 1 kg of sugar plus 1 kg (1 litre) of water requires 75 g of oxalic acid and makes 1.67 litres … enough to treat all the colonies in the association apiary.

Which is not such a bad idea. Make it up carefully once and share it with your fellow beekeepers. Storage details are provided below.

Recipes : Api-Bioxal

Warning – the recipe on the side of a packet of Api-Bioxal makes up a much stronger solution (4.4% w/v) of oxalic acid than has historically been used in the UK. Stronger isn’t necessarily better. The recipe provided is 35 g Api-Bioxal to 500 ml of 1:1 syrup. By my calculations this recipe makes sufficient solution at a concentration of 4.4% w/v to treat 11 hives. 

To make a 3.2% Api-Bioxal-based oxalic acid-containing solution using the 35 g pack of Api-Bioxal you need to mix the entire contents of the pack with 691 ml of 1:1 syrup.

Here’s the maths:

  • 35 g of Api-Bioxal contains only 22.14 g of oxalic acid. 88.6% of the 35 g is oxalic acid dihydrate (the remainder is cutting agents like glucose and powdered silica) and so the oxalic acid content is ((35 * 0.886) * 0.714) = 22.14 g.
  • To calculate the volume of syrup you need to divide it by the final percentage required i.e. (22.14 / (3.2/100)) = 691 ml. I don’t know the exact amount of sugar and water needed to make this amount … it’ll be about 430 g of each (I think).

A 35 g packet of Api-Bioxal is therefore sufficient to treat about 15 colonies (assuming 5 ml per seam, 8 seams per hive and 10% ‘just in case’) at the recommended concentration of 3.2% w/v.

Api-Bioxal is sold in three pack sizes (35 g, 175 g and 350 g). If you are wealthy enough to be able to purchase the larger pack sizes you’ve probably got your own beekeeper (or mathematician). Relax on your yacht while they do the calculations for you 😉

On the other hand … if you have a smaller number of colonies either make a full 35 g packet up and share it, or use accurate scales and the following table:

Api-Bioxal recipes for 3.2% OA trickling

Api-Bioxal recipes for 3.2% OA trickling


Storage of oxalic acid syrup at ambient temperatures rapidly results in the acid-mediated breakdown of sugars (particularly fructose) to generate hydroxymethylfurfural (HMF). As this happens the colour of the oxalic acid-containing solution darkens significantly.

This breakdown happens whether you use oxalic acid or Api-Bioxal.

Stored OA solution and colour change

Stored OA solution and colour change …

HMF is toxic to honey bees at high concentrations. Studies from ~40 years ago showed that HMF concentrations below 30 mg/l were safe, but above 150 mg/l were toxic1. HMF buildup is one way overheated honey is detected.

At 15°C HMF levels in OA solution can reach 150 mg/l in a little over a week. At room temperature this happens much faster, with HMF levels exceeding 150 mg/l in only 2-3 days. In the dark HMF levels build up slightly less quickly … but only slightly 2,3.

Only make up OA solutions when you need them.

If you must store your oxalic acid-containing syrup for any length of time it should be in the fridge (4°C). Under these conditions HMF levels remain well below toxic levels for at least one year. However, don’t store it for this long … use it and discard the excess. Don’t use discoloured oxalic acid solutions as they’ve been stored incorrectly and may well harm your bees.

Please re-read the comments above about the toxicity of oxalic acid. If you are going to store it in the fridge it must be very clearly labelled and there must be no chance that children can reach or open the container.


Api-Bioxal is the least expensive VMD-approved miticide and powdered oxalic acid is much, much cheaper. Both contain the same active ingredient, oxalic acid, which is highly effective against phoretic mites.

In midwinter, with very low levels (or no) of brood, a single oxalic acid-containing treatment minimises mite levels for the coming season.

Oxalic acid-containing solutions are easy to prepare. I recommend you make sufficient for your own colonies and those of your beekeeping friends and association members. My previous BKA used to distribute litres of the stuff for use in midwinter. Use this solution in midwinter and then discard any that is unused.

Oxalic acid-containing solutions are inexpensive and easy to administer by trickling. As I shall demonstrate next time.

Please re-read the safety instructions highlighted in red above.

Michelle Dubois

Michelle Dubois

† Listen very carefully, I shall say zis only once was a catchphrase used by “Michelle of the Resistance” in the 1980’s comedy ‘Allo ‘Allo! Michelle (Dubois) was rarely seen without a trench coat and beret, had a corny French accent and was played by Kirsten Cooke.

‘Allo ‘Allo! ran for 85 episodes in the decade from 1982 on BBC one. It was about a café in Nazi-occupied France and the French Resistance, just about. It mixed bawdy humour with gross stereotypes (posh British twits, sex-obsessed French) and was a parody of ITV’s series Secret Army (’77-’79).

Early episodes had obvious and rather dull titles. In the later series the individual episodes had some quite good puns like Awful Wedded Wife.

Michelle – Listen very carefully, I shall say zis only once

René – Well, in that case, could you please speak slowly?

You had to be there … 😉

‡ Oh alright then, since you insist. The 175 g pack of Api-Bioxal (~£39) needs to be made up in 3.459 litres of 1:1 syrup and the 350 g pack (~£65) 6.919 litres of 1:1 syrup. Determining how much water and sugar to mix to make these amount is, as they say, an exercise for the reader. Assuming a 3.2% solution and 8 seams of bees per colony Api-Bioxal costs between 63p and 41p per hive (see note below), depending upon the pack size you purchase. I know that beekeepers moan on and on about the outrageous cost of Api-Bioxal (as do I), but is 63p per colony really an unreasonable amount to spend on VMD-approved medicines to keep your colony as clear of Varroa as possible? I don’t think so.

Note – the costs in the paragraph were calculated using the lowest prices I could currently find for Api-Bioxal. C Wynne Jones has the 35g packets for £9.50 and Maisemores have the 350g packets for £64.79. Prices correct on 9/10/17.

1 Jachimowich T., El Sherbiny G., Zur Problematik der verwendung von Invertzucker für die Bienenfüttering, Apidologie 6 (1975) 121-143.

2 Bogdanov S., Kilchenman V., Chamere J.D.. Imdorf A. (2001) available online.

3 Prandin, L., Dainese, N. , Girardi, B., Damolin, O., Piro, R., Mutinelli, F. A scientific note on long- term stability of a home-made oxalic acid water sugar solution for controlling varroosis Apidologie, 32:) 451-452


Kick ’em when they’re down

Out, damn'd mite ...

Out, damn’d mite …

Why bother treating colonies in midwinter to reduce Varroa infestation? After all, you probably treated them with Apiguard or Apivar (or possibly even Apistan) in late summer or early autumn.

Is there any need to treat again in midwinter?

Yes. To cut a long story short, there are basically two reasons why a midwinter mite treatment almost always makes sense:

  1. Mites will be present. In addition, they’ll be present at a level higher than the minimum level achievable, particularly if you last treated your colonies in late summer, rather than early autumn.
  2. The majority of mites will be phoretic, rather than hiding away in sealed brood. They’re therefore easy to target.

I’ll deal with these in reverse order …

Know your enemy

DWV symptoms

DWV symptoms

The ectoparasite Varroa feeds on honey bee pupae and, while doing so, transmits viruses (in particular DWV) that can completely mess up the development of the adult bee. Varroa cannot replicate anywhere other than on developing pupae. It’s replication cycle, and the resulting mite levels in the colony, are therefore tightly linked to the numbers and availability of hosts … honey bee pupae.

If developing brood is available the mite can replicate. Under these conditions, newly emerged adult, mated, female Varroa spend a few days as phoretic mites, riding around the colony on young bees. They then select a cell with a late-stage larvae in, enter the cell and wait until pupation occurs. If developing worker brood is available each infested cell produces 1 – 2 new mites (drone cells produce 3+) and mite numbers increase very rapidly in the colony.

In contrast, if there’s no developing brood available, the mites have to hang around waiting for brood to become available. They do this as phoretic mites and can remain like this for weeks or months if necessary.

Therefore, when brood is in abundance and the queen in laying freely mites can replicate to very high levels. In contrast, when brood is limiting and the queen has reduced her egg laying to a   v  e  r  y     s  l  o  w     r  a  t  e     the mite cannot replicate and must be predominantly phoretic.

When does this happen?

Lay Lady Lay … or don’t

Ambient temperature, day length and the availability of nectar and pollen likely influence whether the queen lays eggs. When it’s cold, dark and there’s little or no pollen or nectar coming into the hive the queen slows down, or even stops, laying eggs.

About 8 days after she stops laying there will be no more unsealed brood in the colony. About 13 days after that all the sealed brood will have emerged (along with any Varroa). Therefore, after an extended cold period in midwinter, the colony will have the lowest level of sealed brood … and the highest proportion of the mite population will be phoretic.

Under normal (midsummer) circumstances about 10% of the mite population is phoretic. It’s probably unnecessary to state that, if there’s no brood available, 100% of the mites must be phoretic.

All licensed miticides work extremely well against phoretic mites.

Caveats, guesstimates, global warming and the Gulf Stream

Global warming

Global warming …

Whatever the cause, the globe is warming (irrespective of what Donald Trump tweets). Long, hard winters are getting less common (or perhaps even rarer, as they were never particularly common in the UK). In Central, Southern or Eastern Britain it’s possible that the colony will have some brood present all year. In parts of the West, warmed by the Gulf Stream, I’d be surprised if a colony was ever broodless. Only in the North is it likely that there will be a brood break in midwinter.

Most of the paragraph above is semi-informed guesswork. I don’t think anyone has systematically analysed colonies in the winter for the presence of sealed brood. Sure, many (including me) have opened colonies for a quick peek. Others will have peered intently at the Varroa board to search for shredded wax cappings that indicate emerging brood. The presence of brood will vary according to environmental conditions and the genetics of the bees, so it’s not possible to be dogmatic about these things.

However, it’s safe to say that in midwinter, sealed brood – within which the mites can escape decimation by miticides – is at a minimal level.

Reducing mite levels and minimal mite levels

Within reason, the earlier you apply late summer miticides, the better you protect the all-important overwintering bees from the ravages of viruses, particularly deformed wing virus. This is explained in excruciating detail in a previous post, so I won’t repeat the text here.

However, I will re-present the graph that illustrates the modelled (using BEEHAVE) mite levels.

Time of treatment and mite numbers

Time of treatment and mite numbers

The gold arrow (days 240-300 i.e. September and October) indicates when the winter bees are being reared. These are the bees that need to be protected from mites (and their viruses). Mite numbers (starting with just 20 in the hive on day zero) are indicated by the solid coloured lines. The blue, black, red, cyan and green lines indicate modelled mite numbers when the colony is treated with a miticide (95% effective) in mid-July, August, September, October or November respectively.

The earlier you treat, the lower the mite levels are when the winter bees are being reared. Study the blue and black lines.

This is a good thing.

In contrast, by treating very late (the cyan and green lines) the highest mite numbers of the season occur at the same time as the winter bees are being reared. A bad thing.

But … look also at mite numbers after treatment

Look carefully at the mite numbers predicted to remain at the end of the year. Early treatment leaves higher mite levels at the start of the following year.

This is simply because mites escaping the treatment at the end of summer have had an opportunity to reproduce during the late autumn.

This is why the additional midwinter treatment is beneficial … it kills residual mites and gives the colony the best start to the new calendar year§.

Kick ’em when they’re down

Early treatment protects winter bees but risks exposing bees the following season to unnecessarily high mite numbers. However, in midwinter, these residual mites are much more likely to be phoretic due to a lack of brood in the colony. As I stated earlier, phoretic mites are relatively easy to target with miticides.

So, give the mites a hammering in late summer with an appropriate and effective miticide and then give those that remain another dose of the medicine in midwinter.

But not another dose of the same medicine

Since the majority of mites in a colony with little or no brood will be phoretic, you can easily reduce their numbers using a single treatment containing oxalic acid. This can be administered by sublimation (vaporisation) or by trickling (dribbling).

There’s no need to use any treatment that needs to applied for a month. Indeed, many (Apiguard etc.) are not recommended for use in winter because they work far less well on a largely inactive colony.

Trickle 2 - £1

Trickle 2 – £1

I’ve discussed sublimation previously. However, since this requires relatively expensive (£30 – £300) specialised delivery and personal protection equipment it may be inappropriate for the two hive owner. In contrast, trickling requires almost no expensive or special equipment and – reassuringly – has been successfully practised by UK beekeepers for many years. I did it for years before I bought my Sublimox vaporiser.

Therefore, in two further articles this autumn (well before you’ll need to treat your own colonies) I’ll describe the preparation and storage of oxalic acid solutions and its use.

Be prepared

If you want to be prepared you’ll need to beg, borrow or steal the following – sufficient oxalic acid (or Api-Bioxal), a Trickle 2 bottle sold by Thorne’s, a cheap vacuum flask (Tesco £2.50), granulated sugar and a pair of thin disposable gloves.

Do this soon. Don’t leave it until midwinter. You need to be ready to treat as soon as there’s a protracted cold spell (when brood will be at a minimum). Over the last few years my records show that this has been anywhere between the third week in November and the third week in January.

More soon …

† Only MAQS is effective against mites sealed in cells. This is why most miticides are used for extended periods in the late summer or early autumn … the miticide must be present as Varroa emerge from sealed cells.

‡ I’ll repeat the caveat that this is an in silico simulation of what happens in a beehive. Undoubtedly it’s not perfect, but it serves to illustrate the point well. It’s freely available, runs on PC and Mac computers, and is reasonably well-documented. In the simulations shown here the virtual colony was ‘primed’ with 20 mites at the beginning of the year. BEEHAVE was run using all the default settings – climate, forage etc. – with the additional application of a miticide (95% effective) in the middle of the months indicated. Full details of the modelling have already been posted.

§ The National Bee Unit recommend Varroa levels are maintained below 1000 throughout the season. Without treatment, 20 mites at the start of the season can easily replicate to ~750 in the autumn. If you start the season with 200 mites then levels are predicted to reach ~5000 in the following summer. The colony will almost certainly die that season or the next. There’s a more detailed account of the consequence of winter brood rearing and the level of mite infestation written by Eric McArthur and reproduced on the Montgomeryshire BKA website that’s worth reading.

¶ The cumulative (year upon year) effect of late summer treatment with no midwinter treatment has been discussed previously. I’ll simply re-post the relevant figure here – 5 years of bee (in blue, left axis) and mite (in red, right axis) numbers with only one treatment per season applied in late September. Within two years the higher mite numbers that are present at the start of the year reproduce to dangerously high levels.

Mid September

Mid September

Size matters

Anyone reading the beekeepingforum.co.uk will be aware that there are a number of contributors there that enthusiastically recommend the treatment of colonies with vaporised (or, perhaps more accurately, sublimated) oxalic acid to reduce Varroa levels.

There goes a few pence ...

There goes a few pence …

Although vaporised oxalic acid (OA) has been used by some for many years, the speed with which it has recently been embraced by many UK beekeepers (at least those that contribute to discussion forums and, perhaps to a lesser extent, those I speak to in associations over the winter) probably reflects two or three things:

  • an awareness of just how effective oxalic acid is as a treatment
  • the increased availability of commercial oxalic acid vaporisers (or Heath Robinson-like plans to build-your-own)
  • the huge price-differential between oxalic acid and most other treatments

There are almost as many homegrown or imported vaporisers as there are treatment regimes to hammer down the mite levels. Of course, there’s the contentious point that oxalic acid is not approved by the VMD (Veterinary Medicines Directorate), despite having been in routine use for decades. Api-Bioxal is, but is probably unsuitable for sublimation due to the inert (as far as Varroa are concerned) additives it contains. Api-Bioxal can be vaporised but leaves a caramelised residue in the vaporiser pan that is hard to clean.

Out, damn'd mite ...

Out, damn’d mite …

‘Vaping’ is also popular in the US. Randy Oliver has covered it extensively on his scientificbeekeeping.com site and it’s also regularly discussed on Beesource. OxaVap make/supply a vaporiser that appears very similar to the Sublimox I use. The OxaVap model has a useful temperature display that I would find much easier to read than the red/green diodes on the Sublimox … I’m red/green colourblind.

Active and passive vaporisers

The Sublimox and OxaVap vaporisers are ‘active’ … they blow out a dense cloud of OA-containing vapour through a relatively narrow diameter nozzle (the video below uses water to demonstrate this process). This provides advantages both in terms of ease and speed of delivery. These vaporisers simply need a 7mm hole drilled through the sidewall of the floor (see photo at the top of the page), or through an eke placed over the colony. The OA-containing vapour is ‘squirted’ in, permeates all corners of the hive within seconds and you can then move on to the next hive. The vaporiser doesn’t need cooling between treatments and the dose administered is tightly controlled.

Big Daddy

However, OA dosage isn’t critical. It has been shown to be well-tolerated by bees in studies from groups in the UK and Germany. If the dose isn’t critical and speed really is important then perhaps consider the vmVaporizer. At $3600 it’s about ten times the price of a Sublimox.

vmVaporizer ...

vmVaporizer …

The manufacturers claim you can treat 300 hives an hour with one of these … one every 12 seconds. For comparison, the Sublimox takes 20-30 seconds per hive. However, what takes the time is sealing the hive, moving the generator about, unsealing the hive etc. so you’d need a team of (well protected) helpers and some closely spaced hives to achieve a similar rate. The vmVaporizer is mains (110V) powered so would also need a generator or inverter.

The video above demonstrates the vmVaporizer in action. It produces copious amounts of oxalic acid vapour, albeit less ‘forcefully’ than the Sublimox. It seems the only way to control how much is delivered is by changing the duration the hive is exposed for.

Undoubtedly this is overkill for the majority of readers of this site, but it’s interesting to see what the commercial beekeeping community are using (much like browsing the decapping or bottling machines in the Swienty catalogue). There’s at least one satisfied UK-based beekeeper quoted on the vmVaporizer site so … Mark, if you happen to read this I’d be interested in how well the machine works and whether you can achieve the quoted hive treatment every 12 seconds?

And, does it work with Api-Bioxal?



Get dribbling

There has been a prolonged spell of cold weather in Eastern Scotland. Temperatures have rarely risen above 5°C, with hard frosts overnight. However, a warm front moved in on Tuesday night and the last few days have been significantly warmer. The lack of activity at the hive entrances and a quick peek under the insulation through the perspex crownboards (where fitted) indicated the bees were all tightly clustered during the cold spell. Furthermore, the absence of debris on the removable Varroa monitoring trays fitted to many of the open mesh floors, suggested that little or no brood was being reared.

Ridiculous to the sublime

Ridiculous to the sublime

Varroa counts

Varroa trays ...

Varroa trays …

There was another clue that the colonies are likely broodless. I had been recording the natural Varroa drop of a few colonies over the last month. I did this by simply counting Varroa at each visit, calculated on a mites/day basis. Although generally low (and very low in a few colonies), it had been steadily increasing. This is a good indication there were more phoretic mites in the colony … again, presumably due to the absence of suitable brood for them to parasitise.

It’s worth noting that the natural mite drop is a notoriously unreliable method of accurately determining mite levels in a colony. For example, it’s dependent upon the amount of sealed brood in the colony. With no sealed brood all mites must be phoretic. In contrast, with limitless sealed brood 80-90% of the mites are within cells. However, although estimates from mite drop are not hugely accurate, they are a lot better than doing nothing. The National Bee Unit has published a Varroa calculator. This allows you to use a combination of the mite drop per day, the time of year, length of season and level of drone brood to predict the total numbers of mites in the colony. For some inexplicable reason this asks for the level of drone brood in December … with 0% not being an available option  🙁

Time to treat

With little or no brood in the colonies, now is a perfect time to treat with an oxalic acid-containing preparation to hammer down the remaining mite population. I’ve previously discussed the importance of this midwinter treatment (see Two treatments … a double whammy). In many ways it’s preparation for the season ahead, rather than for the protection of the bees already present in the colony. The lower the mite levels are at the beginning of the season, the longer it will take for the mite population to reach dangerously high levels.



You can model these events using BEEHAVE. This is an interesting in silico model of a beehive. With mite numbers of ~10 at the beginning of the year, maximum levels reached are low to mid-hundreds by late summer, reducing to a couple of hundred the following winter. This assumes no intervening treatment and runs the model using all the default settings. In contrast, using the same parameters but starting the year with ~100 mites, levels peak at between 3000 and 4000 mites, returning to about 1800 in December.

Remember that the National Bee Unit recommends mite levels should not exceed 1000 or there is a risk of “significant adverse effects on the colony”. Therefore, the midwinter treatment is an important preparation for the year ahead, delaying the point at which these dangerously high mite levels are achieved.

Have your hives got less than 100 mites in them now?

Remember also that, with no sealed brood, midwinter is also the ideal time to expose as many mites as possible to the treatment. With the exception of prolonged treatment with hard chemicals like Apistan or Apivar, it’s probably the only time you’ll achieve greater than 95% reduction in mite numbers. With little or no brood present there’s nowhere for the mites to hide.

Dribbling or vaporisation?

An oxalic acid-containing treatment is recommended in midwinter. This can be delivered by dribbling or sublimation (vaporisation). Under optimal conditions, efficacy of the two methods is broadly similar (90%+) though there is some evidence that dribbled oxalic acid is slightly detrimental to colonies (when compared with sublimation, but not when compared to doing nothing).

Sublimox in use

Sublimox in use …

Api-Bioxal is the VMD-approved oxalic acid-containing treatment. If used for dribbling be aware that the suggested concentration on the side of the packet is higher than conventionally used in the UK. It’s also worth noting that it’s not available pre-mixed so has to be made up from powder. In this regard it’s a less useful product than the pre-mixed oxalic acid solution that Thorne’s (and possibly other suppliers) sold each winter. The one- or two-hive beekeeper needs to weigh out very small amounts accurately, or get together with others to make a large batch. Hardly what I’d call progress. Furthermore, the inclusion of glucose and powdered silica (as an anti-caking agent) in Api-Bioxal means it leaves a caramelised mess if used for vaporisation. Although a scouring pad and elbow grease will get rid of this mess, it’s another example of how the “approved” commercial product is actually less good – and no more effective – than the oxalic acid dihydrate that beekeepers have been using for 20 years or more.

Notwithstanding these negative comments, Api-Bioxal works well and is less expensive (per treatment) than most of the other VMD-approved Varroa treatments.

Don’t delay, get out and get dribbling …

The forecast for the next 7-10 days is for significantly warmer temperatures. This means that the queen – if she was having a break from egg-laying – will start laying again. There will be open brood by this weekend and sealed brood in your colonies by about the 15th of December. Dribbled oxalic acid is detrimental to – and may kill – open brood so if this is your preferred method of treatment then don’t delay. If you sublimate you’ve got a few days leeway, but don’t delay any longer than that.

Here are a couple of old videos showing trickling (dribbling) oxalic acid onto a large and small colony in the middle of winter. The Trickle bottle from Thorne’s makes administering the treatment very quick and easy.

Of course, sublimation using an active vaporiser like a Sublimox is even faster and doesn’t involve opening the colony. Here’s an example showing treatment of a recently hived swarm in midsummer … I could have removed the Sublimox after about 30 seconds.

The Daily Mail may be predicting the coldest winter since the last ice age (so perhaps there will be another broodless period§) but I wouldn’t rely on them to influence something as important as the midwinter treatment for reducing Varroa levels.

Here’s a perfect example of the problems encountered by the ‘topical blogger’. I wanted to write about midwinter Varroa treatment in the middle of winter, at a time when others – particular new beekeepers – should be treating their own colonies. Typically these treatments are made in late December or early January. However, the long-range (10 day) forecast in late November suggested the second week of December might be suitable. Some of this was therefore written in very late November, the Varroa drop comments added once I’d completed counting around the 4th to the 6th, and the post finished off the following day once I’d treated my own colonies.

This assumes that the queen started laying on the 7th, the first full day with elevated temperatures.

§ I didn’t open any colonies to confirm they were broodless. I was happy enough to take the clues from the increased mite drop on the Varroa trays and the absence of debris indicating uncapping of brood cells. However, I was told by friends that other colonies they opened on the 7th were broodless.


Out, damned mites

Sublimox vaporiser

Sublimox vaporiser …

Today was very mild, slightly damp and breezy after a prolonged cold spell (at least here in Scotland). The long, cold spell means that colonies are broodless. Now is an ideal time to apply your midwinter Varroa treatment. Don’t wait until the Christmas holidays, don’t wait until the weekend after next … colonies will probably have sealed brood again by then. For maximum effect treat while the colony is broodless and decimate the phoretic mite population.

I treated all my colonies late this afternoon and evening. I finished the last using a headtorch for illumination and tidied up under bright moonlight. The bees looked good and it was great to be doing some beekeeping again, if only briefly.

 A longer post justifying why the colonies were considered broodless and why it is so important to treat when they are broodless will appear this Friday.

The rather weak title is a variant of Shakespeare’s “Out, damned spot” from the play Macbeth. The words are spoken by the sleepwalking Lady Macbeth who is going insane with guilt after her husband killed Duncan (the King of Scotland). The spot refers to Duncan’s blood. Mites on the Varroa tray look like tiny spots of blood …


Those pesky mites

DWV symptoms

DWV symptoms

If you haven’t yet treated your colonies to reduce Varroa levels before the winter arrives it may well be too late. High Varroa levels are known to result in the transmission of virulent strains of deformed wing virus (DWV). These replicate to very high levels and reduce the lifespan of bees. If this happens to the ‘winter bees’ raised in late summer/early autumn there’s a significant chance that the colony will die during the winter.

Mite levels in most of my colonies have been very low this year. Partly due to thorough Varroa management in the 2015/16 winter (the only thing I can take credit for), partly due to the relative sparsity of beekeepers in Fife, partly due to the late Spring and consequent slow build-up of colonies and partly due to an extended mid-season brood break when requeening. Most colonies yielded only a small number of mites (<50) during and after a 3 x 5 day treatment regime (to be discussed in detail in a later post) by sublimation.

Infested arrivals

The low mite drop definitely wasn’t due to operator error or vaporiser malfunction. At the same time I treated a swarm that had moved into a bait hive in early June …

Out, damn'd mite ...

Out, damn’d mite …

This is ~20% of the Varroa tray. Have a guess at the number of mites in this view only. Click on the image to read the full legend which includes the mite count.

The image above was taken on the 18th of September, a day or two after starting the second round of 3 x 5 day treatments. The colony really was riddled. When a colony swarms 35% of the mites in the colony leave with the swarm (or, in this case, arrives with it). For this reason the swarm was treated for mites shortly after it arrived in June. It did have a reasonably high mite load but subsequently built up very quickly and didn’t experience the mid-season brood break my other colonies benefitted from.

The colony now has an acceptable mite drop (<1 per day). Similar colonies are still rearing brood – I’ve not checked this one, but they are bringing in some pollen from somewhere – so there’s a possibility the majority of the remaining mites are tucked away in sealed cells. I’ll keep a close eye on this colony through the next few weeks and will be treating again midwinter to further reduce the parasite burden.

Treat ’em right

If you are treating this late in the season make sure you use a miticide that is appropriate for the conditions. Apiguard (a thymol-containing treatment) is almost certainly unsuitable unless you’re living in southern France as it needs a temperature of 15°C to be effective. MAQS has a recommended temperature minimum of 10°C which may be achievable.

Hard chemicals such as Apivar and Apistan can be used at lower temperatures but there’s little point in treating with Apistan unless you’re certain all your mites are sensitive. They almost certainly are not as Apistan/Bayvarol resistance is very widespread in the UK mite population. Just because you get an increased mite drop in the presence of Apistan does not mean treatment has been effective. Perhaps all you’ve done is killed the sensitive mites in the population, leaving the remainder untroubled. This is what’s known as a bad idea … both for your bees next season and for your neighbours.

 I’m posting this now due to the large number of searches for, and visits to, pages on use of Apiguard or other Varroa treatments. These are currently running second to ‘fondant‘ in one form or another.