In a report, FERA (the UK government Food and Environment Research Agency) examined the issue of 'guttation' following the release of an independent paper by Girolami et al. There was also an experiment conducted by a group of German Beekeepers.
the report, and the Girolami study along with others, it is my opinion
that Fera's assessment of the issue and the Girolami study is misleading,
and in particular, in my view uses flawed studies to deliberately cast
doubt over Girolami's independent, peer reviewed work.
their analysis in relation to guttation and in particular, the Girolami study,
This is misleading, because it is made to sound that the addition of sucrose to all of the guttation fluid combined with the direct feeding to bees, is reason to be suspicious of Girolami’s study – almost giving the impression the bees are deliberately tricked into consuming pesticide.
In actual fact, Girolami added sucrose to only some of the samples, and other bees were fed plain guttation drops. This made no difference to the toxic effects - this significant point is not mentioned.
In addition to which, and following on from the point above, in
regulatory tests for oral toxicity, the 'test pesticides' are mixed with a
sucrose solution anyway!
FERA know this, and they know all about regulatory test methodologies and indeed, Helen Thompson of FERA certainly knows this – she conducted the oral toxicity tests on behalf of Bayer CropScience to support the DAR for imidacloprid.
In these test, Helen Thompson fed bees test solution mixed with sucrose, as described, via feeders.
However, Girolami, was, I believe,
more scientific than the regulatory EPPO guidelines demand.
He discarded bees that did not drink the substance – thus 100% of the test groups had definitely consumed the neonicotinoid being tested. With regulatory tests, the bees get to ‘share among themselves’ the test substance. In other words, for all we know, in regulatory tests, some bees may have taken the substance, some may not (take into account there may be any number of reasons for this, for example, they are anaesthetised first).
Here is an analogy:
Imagine a pharmaceutical drug being tested on humans, who were in a ward and having gained consciousness again following anaesthetic, they can then (voluntarily) help themselves to a drink (or not) from a dispenser (which happens to contain the medicine).
If the same principles were in action for regulating human medicines that are in place for insecticides, then if just one person died, this would this give the pharmaceutical company the right to claim that in the regulatory trial, only 1 person out of 10 had actually died from taking the medicine.
However, this neglects a very crucial question: how many of those 10 people actually took the medicine in this 'voluntary' situation? If only one person took it - the one who died, suddenly the regulatory test does not look so reassuring. Would you want to take a medicine that ad been tested using such methodology?
The point being, that unless we know for sure
all 10 of the patients definitely took the medicine, it would not be correct
for a pharmaceutical company to state 'no negative effects in 90% of
This is why I believe Girolami's methodolgy is more robust, whereas the regulatory methodology is a farce.
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