You have
previously commented that mold sample analysis reports are difficult
to interpret by homeowners, and even by some professionals. Can you
provide a guide for when the “counts” of the most common indoor
fungi (such as Penicillium and Aspergillis) are sufficiently high to
require remediation efforts?-Tim
, California
This is probably one of the most
difficult questions to answer, with the answer being actually useful
to those concerned about what their test results mean.
The mold spore category described
as Aspergillus/Penicillium by commercial laboratories may
include spores of Aspergillus and Penicillium. Also,
depending on the analyst, it may include any spore that is round or
ovoid and in a certain size range. It may include cells/spores such
as those of yeast species, Aureobasidium, Trichoderma,
Paecilomyces, Mucor, Verticillium, Acremonium, and even young
spores of Cladosporium. As such, in some cases, a high count
of Aspergillus/Penicillium may not mean a high count of these
two very important (from a health a health perspective) mold genera.
When I do counts of outdoor mold,
they are typically dominated by Cladosporium and yeast with
lesser concentrations of typical Aspergillus and
Penicillium-type spores. No commercial laboratory to my
knowledge reports yeast concentrations save for the genus Torula.
Yeast are easily recognized by shape, their thin cell walls and
propensity to take up aniline blue stain. These features can only
be seen clearly under 1000X magnification.
Magnification used by
the analyst is also a significant factor in conducting so-called
Aspergillus/Penicillium-type counts. There are many
Aspergillus and Penicillium spores mas well as yeast and
Acremonium, that cannot be seen clearly at the two most
commonly used magnifications of 400 and 600X. Those magnifications
are too low and do not have the resolving power to adequately
detect, identify and count many of the smaller Aspergillus
and Penicillium-type spores. Since most laboratories use
either 400 or 600X magnifications concentrations of Aspergillus/Penicillium
are likely to be significantly under reported. When I compare my
counts to those conducted concurrently in the same environment or in
the same building but at different times it is striking how
commercial laboratory counts under- report actual concentrations
compared to 1000X magnification counts. The lower magnifications
are simply not good enough for the task of counting spores in the
2-3 µm range.
Aspergillus/Penicillium
counting is further confounded by the fact that these two genera
often release their spores in strings. This changes their
aerodynamics and collection on sample media. They often bounce and
then deposited up to several millimeters away from the
deposition trace. Most if not all commercial laboratories count the
deposition trace and no more. As such, particle bounce with
subsequent deposition is not taken into consideration. In some
cases (particularly when Penicillium chrysogenum is
abundant) two thirds of my count at 1000X is spores not found on the
deposition trace.
So what does an Aspergillus/Penicillium
count mean? How much is too much? If the laboratory does not
conduct counts at 1000X and take particle bounce into consideration
reported Aspergillus/ Penicillium concentrations in most
cases are not reliable enough to make important mold-related
decisions.
September 2, 2005