Different methods available for size measurements of fungal and actinomycet
e spores were compared for four fungal species (Penicillium brevicompactum,
Penicillium melinii, Cladosporium cladosporioides, and Aspergillus versico
lor) and two actinomycete species (Streptomyces albus and Thermoactinomyces
vulgaris). The physical size of spores was measured with three microscopic
methods: with an optical microscope from stained (wet) slides, with an opt
ical microscope from unstained (dry) slides and with an environmental scann
ing electron microscope (SEM) directly from the microbial culture. The aero
dynamic diameter, d(a), of airborne spores was measured with an aerodynamic
particle sizer. The respiratory deposition of spores was calculated with a
computer-based model. The environmental SEM measurements indicated larger
size for fungal spores than the optical microscope, whereas for actinomycet
e spores, both microscopes gave comparable results. Optical microscopic mea
surements showed that the stained fungal spores were 1.1-1.2 times larger t
han the unstained ones, which was attributed to the different hydration sta
tus of spores. There was no clear trend in the relationship between the d(a
) and the physical diameter measured with any of three tested microscopic m
ethods. For example, the physical diameter of Cladosporium cladosporioides
spores was larger than the d(a) by a factor ranging from 2.0 to 2.2, wherea
s the d(a) of Streptomyces albus spores was larger than the physical diamet
er by a factor of 1.3 1.5. Thus, the aerodynamic diameter of microbial spor
es cannot be accurately estimated solely based on the physical diameter but
needs information on the density of the spores that may vary considerably.
The results on the spore size were utilized to calculate respiratory depos
ition of spores. The errors in the size measurement were found to result in
overestimation of the respiratory deposition of C cladosporioides spores b
y a factor of 1.2-1.8, and underestimation of the respiratory deposition of
S. albus spores by a factor of 0.6-0.7. These errors in the size measureme
nt cause bias in the exposure assessment and in the estimation of the effic
iency of control devices. More research is needed to standardize the method
for particle diameter estimates applicable for airborne spores.