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- Examining the Validity of Current Indoor Mold Sampling Techniques
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- Opinions based on observations of
- Field investigations 1978-2005
- Sample contents 1986-2005
- By same person making field investigation and lab analysis
- Influenced by academics in aerobiology, mycology, IH, engineering,
sciences
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- Air sampling
- counts (spores/M3 of air) are inaccurate
- causes of particle level variation
- Tape samples – surface selection errors
- Vacuum samples
- surface vs. cavity vs. insulation
- Cultures
- not so great for screening
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- Scan a whole trace at low X
- Count >= 25% of trace at 480x or 720x (ID & count important
particles)
- Calculate Spores/M3 of air for that trace (i.e. for that 6
minute interval)
- Spores/M3 = (raw count/%of trace)x(1000/trace vol)
- Example 17,840 Aspergillus niger spores/M3 of air – BUT how
accurate is this procedure?
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- Problem: extreme variation in airborne particle levels occur over very
short intervals
- Fallacy: interpreting specific “counts” i.e. “air tests,” as “exposure”
without other building diagnosis, may be unreliable
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- It depends …
- A precise count
- -- 11,543 spores/M3
- may be highly inaccurate, off by a factor of
- 10 -- 115,430 spores/M3
- 100 -- 1,154,300 spores/M3
- This means at least 1-2 orders of magnitude of error, misrepresenting
the actual longer term exposure level. Precise doesn’t mean accurate.
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11
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12
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- Building stack effects
- Building ventilation – passive (windows, temperatures)
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- Mechanicals operation Variation - A/C or heat on/off
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- Human/animal presence, even if “sitting still”
- Mechanical disturbance – walk on carpet
- Ceiling fans
- Local environment changes affect spore release (wind on bldg, rain, RH,
temp. season, etc.)
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- The absolute number is “wrong”
- The count interpretation based on building conditions is more important
than the absolute number.
- Cannot interpret a count if there was
- no diagnostic inspection
- no recording of test conditions
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18
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- High spore counts may not correlate with high physical activity
- A previous event may produce high levels of moldy dust in an apparently
clean area
- A large hidden mold reservoir may be present outside the remediation
area
- Relative counts were important
in this case
- Further investigation is needed
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- It Depends.
- High (>10k problem spores/M3) = contaminated (somewhere)
- Medium = ambiguous
- Low = ambiguous (look at species and chains)
- Zero = ambiguous (Was the basement door shut?)
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- Short duration indoor airborne particle counts of spores/M3
of air are
- Subject to extreme variation minute to minute for many reasons
- Not repeatable
- Precise does not mean accurate
- And
- Building conditions affecting the sample need to be documented
- Counts should be interpreted in light of a careful diagnostic
inspection
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- Collect visible mold
- Exposed surfaces or by cavity invasion
- Collect settled dust
- Collect HVAC inlet, supply, filter debris
- Inexpensive, rapid, often definitive
- Spores, Conidiophores, Fungal hyphae
- Other diagnostic particles
- Examine non-viable or culture (maybe)
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- Multiple surfaces – dust screening
- Carpet, furniture, soft-goods
- Support both viable and non-viable qualitative analysis
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- Building insulation – the under-estimated common large mold reservoir in
buildings can be pinpointed
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- Surface vacuums leave important mold structures on the surface (use
tape)
- Vacuums do not collect sticky and non-sticky spores with equal success (use
tape)
- Small-bore wall cavity vacuums are unreliable (compared with test cut)
- Not enough air movement in cavity
- Short Air-O-Cel™ easily overloaded
- Long MCE samples, too few or too costly
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- Settlement plates – “Home Test Kits”
- Rely on gravity, large spores fall faster
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- Settlement plates
- False negative results (Chaetom. & S. chart.)
- Possible false positive results
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- Only 10% of all molds will grow on any culture
- Cultures as screens may be 90% wrong
- What grows in the culture is what likes it
- What does not grow may be what was important
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- MEA grew Cladosporium
- DG-18 grew Aspergillus niger, A. flavus, A. glaucus and Penicillium sp.
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- Great to try to coax out and ID an unknown – if culturable
- Great for photographs – if culturable
- Great for detailed speciation studies – if culturable
- May identify a problem in a building, if culturable - else maybe not:
10% vs. 90%!
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- Works by amplification of nucleic acids (DNA cloning)
- Highly accurate identification to species
- Limited data base (being expanded)
- Ideal to look for a specific mold
- May not be useful as a broad screen –have to look for specific targets
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- Expertise at fungal spore identification PAACB - the only fungal spore
identification certification exam www.paacb.org
- EMLAP/Culture ID/Lab Procedures - AIHA
- Workload – who’s really examining the sample?
- Expertise in microscopy and slide preparation
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- Detect evidence of a hidden problem sufficient to …
- Justify (or not) invasive measures to …
- Find and Map Large Mold Reservoirs
- Permit writing a remediation plan
- And also Provide baseline comparison samples for follow-up
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- Air Samples: Spores/M3 of air may be precise but inaccurate
- Tape samples: collection points are critical
- Vacuums surfaces & insulation-yes, but wall vacs-doubtful
- Cultures: 10% chance (maybe more)
- Investigators should document building conditions affecting sample (simple
“air tests” are ???)
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- Fulltext version of this paper:
- InspectAPedia.com/mold/Mold_Test_Method_Validity.php
- Both full-text and this Power Point version (illustrated) are © 2005
Daniel Friedman all rights reserved
- Contact: Daniel Friedman at InspectAPedia.com/Contact.htm
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