Guest guest Posted January 10, 2011 Report Share Posted January 10, 2011 My experience, if just a thumbnail, these are very low colony counts. Similar to a " clean " house, even some that have been intentionally cleaned for mold contamination (dust/debris). However, there are too many unknown factors to state a conclusion. See other posts by Grimes, Thrasher, myself, for more info on interpreting and sampling for mold -- and how and why and when. So, if you supply more data, like how, when, what, then we might be able to let you know what we really think. For now, stick to the history and current condition of the building to make any decisions, not this single sample. It is probably both invalid and unreliable (these are sampling methods terms, see also more about statistics and sampling). > > Spore Identification Results in Colonies > Bipolaris/Drechslera 1 > Cladosporium 3 > Curvularia 1 > Nigrospora 2 > Penicillium 1 > Non-sporulating fungi 4 > Chlamydospores 1 > Total Result: 13 > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2011 Report Share Posted January 10, 2011 If this is a single air sample. The answer is not necessarily so. Have you had water intrusion? Did they test for moisture content of interior and exterior walls, did they inspect and test wall cavities as well as the attics? I am sure Carl will produce additional questions. [] Are these " ok " levels for a home??? Spore Identification Results in Colonies Bipolaris/Drechslera 1 Cladosporium 3 Curvularia 1 Nigrospora 2 Penicillium 1 Non-sporulating fungi 4 Chlamydospores 1 Total Result: 13 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2011 Report Share Posted January 10, 2011 Levels and types by themselves do not determine is a home is " Okay. " Much more information is needed. Are these air samples or surface samples? Collection method and length of sampling time or area of collection. Cultured or microscopy? If cultured what type of agar? Which lab? Type of building. Where in building. History of water damage, if any. Geographic location and climate. Are you sick while in the house? Feel better when you leave only to feel worse upon return? What are your known allergies, respiratory conditions, and other reactions and symptoms? All these and more are critical to any meaningful interpretation of any lab results. These are spore results only. There can be massive mold growth present without detectable spores. All sampling methods tend to see only select items. Bacteria often plays a larger role than mold. And these are but some of the reasons why there are no established levels like there are for radon or asbestos or carbon monoxide, for example. I'd you could send me the lab report several of the questions will be answered. Carl Grimes Healthy Habitats LLC (fm my Blackberry) [] Are these " ok " levels for a home??? Spore Identification Results in Colonies Bipolaris/Drechslera 1 Cladosporium 3 Curvularia 1 Nigrospora 2 Penicillium 1 Non-sporulating fungi 4 Chlamydospores 1 Total Result: 13 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2011 Report Share Posted January 10, 2011 From: Carl Grimes Sent: Monday, January 10, 2011 1:00 PM Sick Buildings Subject: Re: [] Are these " ok " levels for a home??? Levels and types by themselves do not determine is a home is " Okay. " Much more information is needed. Are these air samples or surface samples? yes they are air samples. “Settling†samples is what it was called. Purchased a kit at Home Depot and mailed the petri dish in to a lab called ProLabs. Collection method and length of sampling time or area of collection. You place the petri dish and leave it open for one hour where you want to test the air. After one hour is complete, you then replace the lid and allow to incubate for 48 hours. Cultured or microscopy? If cultured what type of agar? Microscopy, I believe. Not sure about what type of agar. Which lab? ProLab/SSPTM Inc. in FL Type of building. Where in building.- Residential. Fort Worth, TX History of water damage, if any.- Yes home apparently got drenched during the building process and since had numerous leaks due to plumbing issues. Geographic location and climate- Southwest Region and it’s a dry climate. Are you sick while in the house? Always!! Feel better when you leave only to feel worse upon return? Yes What are your known allergies, respiratory conditions, and other reactions and symptoms? Prior to living in this home, we had no known allergies or respiratory conditions expect for my son (who has had allergies since he was three but know has chronic asthma and horrible allergies). We now all suffer from constant respiratory complications, nose bleeds, constant headaches, swollen, itchy eyes, dermatitis, extreme fatigue, and symptoms similar to the common cold. All these and more are critical to any meaningful interpretation of any lab results. These are spore results only. There can be massive mold growth present without detectable spores. All sampling methods tend to see only select items. Bacteria often plays a larger role than mold. And these are but some of the reasons why there are no established levels like there are for radon or asbestos or carbon monoxide, for example. I'd you could send me the lab report several of the questions will be answered. Carl Grimes Healthy Habitats LLC (fm my Blackberry) [] Are these " ok " levels for a home??? Spore Identification Results in Colonies Bipolaris/Drechslera 1 Cladosporium 3 Curvularia 1 Nigrospora 2 Penicillium 1 Non-sporulating fungi 4 Chlamydospores 1 Total Result: 13 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2011 Report Share Posted January 10, 2011 While searching on " Chlamydospores, " because I wasn't familiar with it, I found the following: First, Chlamydospores are developed by the fungi commonly known as the " fairy ring mushroom " because it grows in a circle on the ground. It's a mushroom, not usually associated with WDB, or health effects unless perhaps if you eat it. More telling, it illustrates how the food (agar) in a culture plate changes not just what grows, but how it grows, giving different identifications and names. 2.0% malt agar produces different results than 0.2%. " In Marasmius oreades germination of a basidiospore on 2.0 % malt agar gives a relatively long, narrow germ-tube that soon branches to produce a mycelium. However, on 0.2 % malt agar either the basidiospore gives a short, fat germ-tube which soon ceases to grow and in which a single chlamydospore is formed, or a chlamydospore is formed within the basidiospore without any germ-tube being produced. " In the original post, all of the identified organisms can (or are) typical in outside air not indicating a " problem. " However, if the Chlamydospore is from a mushroom growing inside the home then that most likely is a problem. One of long term dampness. It takes a very long time for mushrooms to grow on building materials. I wouldn't expect the Chlamydospore to be a health risk but because the long term dampness will most certainly have bacteria, biofilm, and the associated filth there may well be a " problem. " If there are health effects then they certainly are showing up with these results, demonstrating once again we need more than numbers. Carl Grimes Healthy Habitats LLC ----- I think it will help if we all have a clearer understanding of what mold is and what it isn't. Google has some really good photos which can be accessed by searching for " mold growth " and then clicking on " Images. " What you see is often like the first image (and most of the others). This iconic image by Terry Brennan shows colonies of a variety of types of mold resulting from airborne moisture flow through the top of the door and across the ceiling. It is not growing on the walls. Where you sample will make a huge difference in the lab results. The image 3rd to the right is much different. Mold is growing on the walls but not the ceiling because the water source soaked up the drywall from the floor. Also, notice how the color changes right near the top of the growth. Different mold because of slightly different moisture levels at the edge of the dampness. If this area were to be sampled you would get drastically different results based on the exact location of the sample. If any of the above mold growth were sporulating then their spores, along with others having nothing to do with the situation, might show up depending on the type of sample, where collected, etc etc. BTW, I've seen air samples from rooms like many in these images with the conclusion that " there is no mold problem. " Because of the assinine and discredited methods of interpreting results, plus the bias of who collected the samples. But that is for another time. Scrolling down you will see " Page 2 " and the first image is a culture plate with mold growth. It looks much different than the previous images for obvious reasons and because it is from a settling plate. Only the spores in the air which are alive and which are heavy enough to settle from the air and happen by chance to land on the plate which has the right kind of food (agar) will grow. They may or may not be from the " growth " in the previous images. What none of these show is bacteria, actinomycetes, and anything other then mold *growth.* The growth, or colony, is what is visible. Spores are the seeds and are too small to see with the naked eye. Got to Page 4 and the first image shows spores flowing from a single stalk of the mold growth colony. All of which is too small to see with the naked eye. Page 5, second down, left side. This identifies some of the many parts of a mold growth colony. The illustration below it is a diagram of mold growth. BTW, the MC (moisture content of the surface) will determine whether or not mold spores will germinate and form colonies. Of all the different types of spores always in the air only some will grow. Change the MC slightly and different ones will grow. BTW, the surface with MC where the mold is growing is where the " biofilm " will form. It is not automatic and is not part of the mold " plant. " It is a film of dampness along with dust, old mold, bacteria and other " filth " which accumulates on the surface over time. As it develops other molds and bacteria previously unable to grow may now start to " make babies " and further populate their little " city " called a " biofilm. " Go back to the culture plate on Page 2. What you see is mold growth which will have some spores. But the massive amount of substance is " biomass " and not spores. Which is part of what Dr Thrasher means when he says about mold, " It's more than just spores. " But it means much more. With dampness there will also be growth of bacteria. It just doesn't grow in a way we can see it and few test for it. General samples for bacteria is limited to the shape (rod, cone, spiral) and whether it changes color with a stain (gram positive) or doesn't (gram negative). Carl Grimes Healthy Habitats LLC Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2011 Report Share Posted January 10, 2011 As the late great Dr Marinkovich told me, you can't get better with 4 or more colony's From: Carl Grimes <grimes@...> Subject: Re: [] Are these " ok " levels for a home??? " Sick Buildings " < > Date: Monday, January 10, 2011, 10:00 AM Levels and types by themselves do not determine is a home is " Okay. " Much more information is needed. Are these air samples or surface samples? Collection method and length of sampling time or area of collection. Cultured or microscopy? If cultured what type of agar? Which lab? Type of building. Where in building. History of water damage, if any. Geographic location and climate. Are you sick while in the house? Feel better when you leave only to feel worse upon return? What are your known allergies, respiratory conditions, and other reactions and symptoms? All these and more are critical to any meaningful interpretation of any lab results. These are spore results only. There can be massive mold growth present without detectable spores. All sampling methods tend to see only select items. Bacteria often plays a larger role than mold. And these are but some of the reasons why there are no established levels like there are for radon or asbestos or carbon monoxide, for example. I'd you could send me the lab report several of the questions will be answered. Carl Grimes Healthy Habitats LLC (fm my Blackberry) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2011 Report Share Posted January 10, 2011 a, Did Dr. Marinkovich say if those were 4 colonies per sq inch, or per cubic meter, or some other measure? I'm not familiar with his method of interpretation or sampling but I'd guess he was talking about 4 colonies on a settling plate. One study I'm familiar with correlated settling plate numbers to Andersen sampler numbers. One colony on a plate was equavalent to 700-1200 on an Andersen sampler. If my guess is he used settling plates then I'd agree with the 4 colonies being too much but qualify it to say something like, " Four colonies on a sampling plate is too much because each colony may represent from 700-1200 others which were not detected. Including spores which settled but didn't grow plus fragments of spores and hyphae containing allergens, irritants, and toxins could increase the equivalent numbers by as much as 1000 times more. " 4 times 1200 is 4800, times 1000 is 4,800,000. The problem is these are extremely rough guesses and estimations of what might be. To fine tune it find out if the 4 spores actually represent 4.8M or if there were only 4 spores present and the plate captured them all requires additional methods and techniques. Even then, absolute or definitive conclusions are tough to come by. BTW, I'm not commenting on Dr Marinkovich or his treatment. Only on how mold spores are measured by various methods. Neither am I discounting the effects of mold. What I am saying is there are no methods which can quantify " mold " and its effects on people in general with anything even approaching accuracy. Which is but one reason why mold data is so easy to shoot down in court. Carl Grimes Healthy Habitats LLC ----- As the late great Dr Marinkovich told me, you can't get better with 4 or more colony's From: Carl Grimes <grimes@...> Subject: Re: [] Are these " ok " levels for a home??? " Sick Buildings " < > Date: Monday, January 10, 2011, 10:00 AM Levels and types by themselves do not determine is a home is " Okay. " Much more information is needed. Are these air samples or surface samples? Collection method and length of sampling time or area of collection. Cultured or microscopy? If cultured what type of agar? Which lab? Type of building. Where in building. History of water damage, if any. Geographic location and climate. Are you sick while in the house? Feel better when you leave only to feel worse upon return? What are your known allergies, respiratory conditions, and other reactions and symptoms? All these and more are critical to any meaningful interpretation of any lab results. These are spore results only. There can be massive mold growth present without detectable spores. All sampling methods tend to see only select items. Bacteria often plays a larger role than mold. And these are but some of the reasons why there are no established levels like there are for radon or asbestos or carbon monoxide, for example. I'd you could send me the lab report several of the questions will be answered. Carl Grimes Healthy Habitats LLC (fm my Blackberry) ---------- The following section of this message contains a file attachment prepared for transmission using the Internet MIME message format. If you are using Pegasus Mail, or any other MIME-compliant system, you should be able to save it or view it from within your mailer. If you cannot, please ask your system administrator for assistance. ---- File information ----------- File: DEFAULT.BMP Date: 15 Jun 2009, 23:10 Size: 358 bytes. Type: Unknown Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2011 Report Share Posted January 10, 2011 Thanks Carl He would suggest a plate in room open for only 20 min where you thought you had concerns.  If you were colonized he wanted to make sure you were not getting re-exposed.   He said anything over 4 colonies was not good.   a From: Carl E. Grimes <grimes@...> Subject: Re: [] Are these " ok " levels for a home??? Date: Monday, January 10, 2011, 3:50 PM a, Did Dr. Marinkovich say if those were 4 colonies per sq inch, or per cubic meter, or some other measure? I'm not familiar with his method of interpretation or sampling but I'd guess he was talking about 4 colonies on a settling plate. One study I'm familiar with correlated settling plate numbers to Andersen sampler numbers. One colony on a plate was equavalent to 700-1200 on an Andersen sampler. If my guess is he used settling plates then I'd agree with the 4 colonies being too much but qualify it to say something like, " Four colonies on a sampling plate is too much because each colony may represent from 700-1200 others which were not detected. Including spores which settled but didn't grow plus fragments of spores and hyphae containing allergens, irritants, and toxins could increase the equivalent numbers by as much as 1000 times more. " 4 times 1200 is 4800, times 1000 is 4,800,000. The problem is these are extremely rough guesses and estimations of what might be. To fine tune it find out if the 4 spores actually represent 4.8M or if there were only 4 spores present and the plate captured them all requires additional methods and techniques. Even then, absolute or definitive conclusions are tough to come by. BTW, I'm not commenting on Dr Marinkovich or his treatment. Only on how mold spores are measured by various methods. Neither am I discounting the effects of mold. What I am saying is there are no methods which can quantify " mold " and its effects on people in general with anything even approaching accuracy. Which is but one reason why mold data is so easy to shoot down in court. Carl Grimes Healthy Habitats LLC ----- As the late great Dr Marinkovich told me, you can't get better with 4 or more colony's Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2011 Report Share Posted January 10, 2011 Thanks, a. That's a decent screening method for potential exposure of the occupied environment within the context of his medical practice rather then just numbers by themselves. However, they would be of no help (actually a hinderance) in litigation or for medical diagnosis of a specific disease. Carl Grimes Healthy Habitats LLC ----- Thanks Carl He would suggest a plate in room open for only 20 min where you thought you had concerns. If you were colonized he wanted to make sure you were not getting re-exposed. He said anything over 4 colonies was not good. a From: Carl E. Grimes <grimes@...> Subject: Re: [] Are these " ok " levels for a home??? Date: Monday, January 10, 2011, 3:50 PM a, Did Dr. Marinkovich say if those were 4 colonies per sq inch, or per cubic meter, or some other measure? I'm not familiar with his method of interpretation or sampling but I'd guess he was talking about 4 colonies on a settling plate. One study I'm familiar with correlated settling plate numbers to Andersen sampler numbers. One colony on a plate was equavalent to 700-1200 on an Andersen sampler. If my guess is he used settling plates then I'd agree with the 4 colonies being too much but qualify it to say something like, " Four colonies on a sampling plate is too much because each colony may represent from 700-1200 others which were not detected. Including spores which settled but didn't grow plus fragments of spores and hyphae containing allergens, irritants, and toxins could increase the equivalent numbers by as much as 1000 times more. " 4 times 1200 is 4800, times 1000 is 4,800,000. The problem is these are extremely rough guesses and estimations of what might be. To fine tune it find out if the 4 spores actually represent 4.8M or if there were only 4 spores present and the plate captured them all requires additional methods and techniques. Even then, absolute or definitive conclusions are tough to come by. BTW, I'm not commenting on Dr Marinkovich or his treatment. Only on how mold spores are measured by various methods. Neither am I discounting the effects of mold. What I am saying is there are no methods which can quantify " mold " and its effects on people in general with anything even approaching accuracy. Which is but one reason why mold data is so easy to shoot down in court. Carl Grimes Healthy Habitats LLC ----- As the late great Dr Marinkovich told me, you can't get better with 4 or more colony's ---------- The following section of this message contains a file attachment prepared for transmission using the Internet MIME message format. If you are using Pegasus Mail, or any other MIME-compliant system, you should be able to save it or view it from within your mailer. If you cannot, please ask your system administrator for assistance. ---- File information ----------- File: DEFAULT.BMP Date: 15 Jun 2009, 23:10 Size: 358 bytes. Type: Unknown Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 11, 2011 Report Share Posted January 11, 2011 Wow. Is all I can say. Well, and this: The whole settling plate method is full of validity and reliability issues. I'm certain that " one hour " in the middle of a room would in no way be representative of the potential exposure. Just someone (or somedog) walking by could invalidate the results. The point of 4 colonies too much, only if they are species that matter. In other words, the Dr. was saying he was looking for pathogenic species in roomos where " infected " patients were going to live. Hence, he was concerned about those relatively few that actually can infect a person. I am very uncomfortable with the website lab that accompanies the cleaner website; it has no info at all, only an order form for " gravity plates " , $64.00. All other is signup/signin. Why is it not public? The cleaner website is typical product marketing website. Nothing special. Like Carl said, this gets very confusing with different agencies (EPA or FDA) and the ability of a manufacturer to keep some ingredients secret (i.e., proprietary) from the user. Again, the product should not only be careully reveiwed, it should be tested by any user who is concerned with effects because of known or suspect sensitivities to specific or generic chemicals. I am always uncomfortable with fogging unless for very specific purpsoses. It is really best at " knocking down " airborne particulates, and second for an immediate surface kill in large growth situations where we want to put people in place for cleanup. But, then you can use just about any cleaner solution to achieve the effect. And you must go in asap to clean (remove) and dry. > > Thanks Carl > He would suggest a plate in room open for only 20 min where you thought you had concerns.  If you were colonized he wanted to make sure you were not getting re-exposed.   He said anything over 4 colonies was not good.   > > a > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 11, 2011 Report Share Posted January 11, 2011 Am I missing something? The CFU counts you reported were not only single digit, some were only 1. That is nearly nothing. The ability to find under 10 CFU's is not hard. I would be generally not concerned if I could trust the methodology of the collection (see Carls description, and many others). but I don't. If there is a good inspection, you can put these in perspective. (Remeber, all comparisons must be relative to other things) Again, if there was visible mold growth, these concentrations are very small and indicate little sporulation or disturbance of the growth. If there is no known growth in the space, then these indicate very little outside air infiltration. It'd be interesting for you to repeat this but add another plate outdoors. It might lead to interesting analyses of the indoors and your exposures. Then, if you have the money, repeat this another time under different weather conditions. > > Thanks, a. That's a decent screening method for potential > exposure of the occupied environment within the context of his > medical practice rather then just numbers by themselves. > However, they would be of no help (actually a hinderance) in > litigation or for medical diagnosis of a specific disease. > > Carl Grimes > Healthy Habitats LLC > > ----- > Thanks Carl > He would suggest a plate in room open for only 20 min where you > thought you had concerns. If you were colonized he wanted to make > sure you were not getting re-exposed. He said anything over 4 colonies > was not good. > > a > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 11, 2011 Report Share Posted January 11, 2011 I have a question, the counts seemed to me to be very good and very low, say those results were taken with air testing in a room were there was carpet and traffic , what about accummalation of " filth " spores fragments,ect. in a WDB situation? how would you get that low of a count inless there wasn't a mold problem? I know discusion was on plates but aridginal post from plates or air testing? with plates would there also be a difference in say one tiny spot of growth vs. the plate being full of multiple growths? > > Am I missing something? The CFU counts you reported were not only single digit, some were only 1. That is nearly nothing. The ability to find under 10 CFU's is not hard. > I would be generally not concerned if I could trust the methodology of the collection (see Carls description, and many others). but I don't. > If there is a good inspection, you can put these in perspective. > (Remeber, all comparisons must be relative to other things) > Again, if there was visible mold growth, these concentrations are very small and indicate little sporulation or disturbance of the growth. If there is no known growth in the space, then these indicate very little outside air infiltration. > It'd be interesting for you to repeat this but add another plate outdoors. It might lead to interesting analyses of the indoors and your exposures. > Then, if you have the money, repeat this another time under different weather conditions. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 11, 2011 Report Share Posted January 11, 2011 , The original post only had numbers. We don't know if those were colony forming units (CFUs from culturing) or spore counts (microscopy). Carl Grimes Healthy Habitats LLC ----- Am I missing something? The CFU counts you reported were not only single digit, some were only 1. That is nearly nothing. The ability to find under 10 CFU's is not hard. I would be generally not concerned if I could trust the methodology of the collection (see Carls description, and many others). but I don't. If there is a good inspection, you can put these in perspective. (Remeber, all comparisons must be relative to other things) Again, if there was visible mold growth, these concentrations are very small and indicate little sporulation or disturbance of the growth. If there is no known growth in the space, then these indicate very little outside air infiltration. It'd be interesting for you to repeat this but add another plate outdoors. It might lead to interesting analyses of the indoors and your exposures. Then, if you have the money, repeat this another time under different weather conditions. > > Thanks, a. That's a decent screening method for potential > exposure of the occupied environment within the context of his > medical practice rather then just numbers by themselves. > However, they would be of no help (actually a hinderance) in > litigation or for medical diagnosis of a specific disease. > > Carl Grimes > Healthy Habitats LLC > > ----- > Thanks Carl > He would suggest a plate in room open for only 20 min where you > thought you had concerns. If you were colonized he wanted to make > sure you were not getting re-exposed. He said anything over 4 colonies > was not good. > > a > > ---------- The following section of this message contains a file attachment prepared for transmission using the Internet MIME message format. If you are using Pegasus Mail, or any other MIME-compliant system, you should be able to save it or view it from within your mailer. If you cannot, please ask your system administrator for assistance. ---- File information ----------- File: DEFAULT.BMP Date: 15 Jun 2009, 23:10 Size: 358 bytes. Type: Unknown Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 11, 2011 Report Share Posted January 11, 2011 OK, I thought it was from plates, hence CFU's. Either way, CFU's or Spore counts (would have to be raw count i.e., actual, not concentration based on sampling rate, to get that low, right?) It's still very very low, nearly impossible to get that low without very good air scrubbing/cleaning, or lots of snow! > > , > > The original post only had numbers. We don't know if those were > colony forming units (CFUs from culturing) or spore counts > (microscopy). > > Carl Grimes > Healthy Habitats LLC > Quote Link to comment Share on other sites More sharing options...
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