Regulatory Compliance 245 Albany Avenue Thornwood, New York (914) Indoor Air Quality Screening At. Scarsdale UFSD

Transcription

1 Regulatory Compliance 245 Albany Avenue Thornwood, New York (914) Indoor Air Quality Screening At Scarsdale UFSD Greenacres School 41 Huntington Avenue Scarsdale, NY RegCom s Project Numbers SUFSD IAQ SUFSD IAQ Date of Survey: October 11, 2017 October 28, 2017 Field Work Performed by: Ernest Coon, MS, RPIH, HEM Nicholas Coon, BS Stephen Coon, BS Report Written by: Ernest Coon, MS, RPIH, HEM November 21, 2017 i

2 ABSTRACT The Scarsdale UFSD retained Regulatory Compliance to conduct an indoor air quality (IAQ) at the Greenacres School, due to staff complaints about a possible indoor air quality concern, the District has decided to take a proactive approach and conduct an indoor air quality to determine the health status of the affected areas. An IAQ involves the use of detector tubes/grab samples to determine if further investigation is warranted. The detector tubes are accurate enough to determine the hazards in the workplace. Detector tube pump systems are very effective way to conduct on-the-spot air monitoring and meet the OSHA requirement of 25% error. Samples were collected in pre-identified areas in the building. The organisms identified in the majority of the indoor air samples collected are typically those found in the air from the exterior of the building and no action is required. The non-classroom side of the basement had a MoldSCORE that ranged from A MoldSCORE rating greater than 150 indicates a moderate probability that the spores originated from inside the building and greater than 250 indicates a high probability. The MoldSCORE along with visual observations have concluded that fungal growth has occurred in the basement boiler room. The organisms identified in the indoor air samples collected in the Psychologist Office, classroom 7A and room 9, had a MoldSCORE range from , consisting of Smuts, Periconia and Myxomycetes, which are typically outdoor organism/plant pathogens. The MoldSCORE for these classrooms is an artificiality and can occur when specific spore types are high outdoors and infiltrate into a building on a certain day (as does pollen) but remain indoors and then exceed outdoor levels that have subsequently decreased. This can be and is commonly seen with obligate plant parasites, such as rust fungi or tree pathogens that never colonize indoor spaces, yet can occur indoors in excess of outdoor levels on given days. Therefore, the organisms identified in the indoor air samples are those found in the air from the exterior of the building and no action is required. The organism identified in classroom 2B, classroom 22, classroom 35 and the Teacher s Lounge had a MoldScore range from , which indicates that there is a moderate probability that the spores originated inside the classrooms. Mold growth was visually identified in the Teacher s Lounge, beneath the contact paper in the cabinet beneath the sink. Bioaerosol sampling only represents a snap shot in time and the true average concentration of microorganisms may differ. ii

3 Molds are part of the natural environment, and can be found everywhere, indoors and outdoors. They are found in schools, homes, hospitals, industry etc. Outdoors, molds play a part in nature by breaking down dead organic matter such as fallen leaves and dead trees. It is impossible to get rid of all mold and mold spores indoors; some mold spores will be found floating through the air and in house/school dust. However, mold is not usually a problem, unless it begins growing indoors and not appropriately corrected. Mold exposure can irritate the eyes, skin, nose, throat, and lungs of both mold-allergic and non-allergic people. Symptoms other than the allergic and irritant types are not commonly reported as a result of inhaling mold. The bioaerosol results for Greenacres School are typical of findings that RegCom has identified in other public schools, hospitals etc. over the past 20 years. Greenacres school has a few isolated areas that need attention or further investigation if recommended actions fail to correct the situation. The average concentration for nuisance dust, formaldehyde, ozone, nitrogen dioxide carbon monoxide, carbon dioxide and total petroleum hydrocarbons were below or equal to the outside sample. It is recommended for the basement (non-classroom areas) that the school inspect, discard suspected moldy contaminated material, clean and disinfect the area, clean the courtyard basement stairwell, install dehumidifiers (if humidity levels remain elevated), and ventilate the basement. For the four (4) areas, classroom 2B, 35, 22 and the Teacher s Lounge had a MoldScore above 150 and it is recommended that the school clean and disinfect all surfaces, clean and disinfect the areas beneath the sinks and remove any contact paper, replace any damaged/stained ceiling tiles, clean and disinfect window air conditioning units. Inspect and ensure that the unit ventilators are clean and that filters changed periodically. There are other recommendations included in the report. None of the information contained herein should be construed as medical advice. Only a qualified physician should make any decision relative to medical significance. iii

4 TABLE OF CONTENTS ABSTRACT TABLE OF CONTENTS ii iii 1.0 INTRODUCTION Reason for Choosing the Sampling Parameters Sampling Methodology RESULTS OBSERVATIONS AND DISCUSSION Carbon dioxide (CO 2 ) Carbon monoxide (CO) Nitrogen dioxide (NO 2 ) Ozone (O 3 ) Formaldehyde (HCHO) Total petroleum hydrocarbons (TPH) Total nuisance dust Temperature and Humidity Biological sampling Carpets, throw rugs and upholstery (throw cushions) Asthma Building Inspection CONCLUSION RECOMMENDATIONS 11 Appendix Appendix A Microbiological Sample Results iv

5 1.0 INTRODUCTION The Scarsdale UFSD retained Regulatory Compliance to conduct an indoor air quality (IAQ) at the Greenacres School, due to staff complaints about a possible indoor air quality concern, the District has decided to take a proactive approach and conduct an indoor air quality to determine the health status of the affected areas. An IAQ involves the use of detector tubes/grab samples to determine if further investigation is warranted. The detector tubes are accurate enough to determine the hazards in the workplace. Detector tube pump systems are very effective way to conduct on-the-spot air monitoring and meet the OSHA requirement of 25% error. Environmental Conditions (10/11/17): 71 0 F and 63% RH. Precipitation event: None Environmental Conditions (10/28/17): 58 0 F and 51% RH. Precipitation event: Rain A baseline IAQ was conducted to determine if the concerns were related to the environment of the building. The investigation consisted of the following: Carbon monoxide (CO) Carbon dioxide (CO 2 ) Nitrogen dioxide (NO 2 ) Ozone (O 3 ) Formaldehyde (CHO) Total Petroleum Hydrocarbons (TPH) Biological sampling Temperature (T) Total nuisance dust Relative humidity (RH) 1.1 REASON FOR CHOOSING THE SAMPLING PARAMETERS Carbon monoxide (CO): is an odorless, colorless gas that interferes with the delivery of oxygen in the blood to the rest of the body. It is produced by the incomplete combustion of fuels. The major sources of CO are cigarettes, motor vehicles, and defective combustion equipment such as furnaces, boilers and hot water heaters. Problems can arise from improper installation, maintenance and inadequate ventilation. 1

6 1.1.2 Carbon dioxide (CO 2 ): in the ranges encountered in the indoor environment does not constitute a health hazard. Carbon dioxide is a normal constituent of exhaled breath and, if monitored, can be used as a screening technique to evaluate whether adequate quantities of outside air (OA) is being introduced into the building. As carbon dioxide levels rise, it indicates that the ventilating system is malfunctioning or the design occupancy of the room is being exceeded. When this happens, a buildup up of common indoor air pollutants can occur, leading to discomfort or health complaints. Inadequate ventilation is a major cause of health complaints such as, respiratory, eye, nose, and throat irritation, lethargy and headaches Nitrogen Dioxide (NO 2 ) is a combustion product from furnaces, motor vehicles, welding and combustion equipment. NO 2 is a colorless, gas that can cause headaches, nausea, dizziness, vomiting, coughing and irritation of the respiratory tract, shortness of breath, and increased incidences of respiratory illness. Children and individuals with asthma and other respiratory illness are at greater risk from exposure to nitrogen oxides Ozone (O 3 ) is a pollutant from automobile pollutant and sunlight, lighting, electronic equipment, electrostatic air cleaners and copy machines. Ozone can be irritating to the eyes, mucous membranes and cause upper respiratory tract irritation Formaldehyde (HCHO) is a colorless, organic compound of carbon, hydrogen and oxygen having the formula HCHO. It is used extensively in industry in the production of synthetic urea and urea-formaldehyde resins, which themselves are widely used as adhesives in making particle board, laminates, plywood and other wood products. Many adhesives and glues also contain this compound, including some used for carpets and wallpaper coverings, and other widely used product-containing formaldehyde is ureaformaldehyde foam insulation. Formaldehyde is also used as a flame retardant for fabrics. Other sources include bulked stored paper products, some cosmetic products, combustion processes including smoking, and atmospheric photochemical smog. The potential for formaldehyde products to be present in the building air is considerable. The main concern is the potential for out-gassing. Airborne formaldehyde can cause irritation to the eyes nose, throat, and the respiratory tract. Prolonged exposure can cause sanitization and/or allergic reactions Total Petroleum Hydrocarbons (TPH) is a term used to describe a large family of several hundred chemical compounds that originally come from crude oil. Crude oil is used to make petroleum products, which can contaminate the environment. Because there are so many different chemicals in crude oil and in other petroleum products (Tar from roofing compounds), it is not practical to measure each one separately. However, it is useful to measure the total amount of TPH at a site. Most people can withstand short exposures to fuel oil vapors without any problems. However, breathing fuel oil vapors overtime can affect a person's ability to smell and taste. High levels can cause headaches, nausea, light-headedness, poor coordination, increased blood pressure and difficulty concentrating. Most people can smell oil vapors at levels as low as 0.1 parts per million (ppm) in air. 2

7 1.1.7 Total Nuisance Dust is the amount of dust found in the air and the health hazards include itching and irritation to the skin and upper respiratory system, respiratory infection, and aggravation of existing respiratory or cardiovascular disease in elevated levels Temperature (T) and Relative Humidity (RH) are considered thermal comfort variables and should not be overlooked. The majority of indoor air quality (IAQ) complaints are related to these 2 parameters. Furthermore, temperature and humidity are variables that affect other indoor air contaminates. American Society of Heating, Refrigeration, and Air Conditioning Engineers (ASHRAE) has published guidelines describing thermal environmental conditions (ASHRAE Standard , Thermal Environmental Conditions for Human Occupancy). These guidelines are intended to achieve thermal conditions in a given environment that at least 80% of the persons who occupy that environment will find acceptable or comfortable. Temperature and humidity are comfort parameters that have been cited as the source of over 35% of indoor air quality complaints. Dry air can affect the human body by causing respiratory ailments such as asthma, bronchitis, sinusitis, and nosebleeds, or general dehydration since the body fluids are depleted during respiration. Skin moisture evaporation can cause skin irritations and eye itching and the apparent temperature of the air is lower than what the thermometer indicates and the body feels colder Bioaerosols are airborne particles, large molecules, or volatile compounds that are living or were released from a living organism. The concern regarding the indoor environments is centered on fungi. Fungi are ubiquitous organisms that can be found in indoor environments wherever food and moisture conditions are conducive to their growth. The microorganisms found in outdoor air grow on moist surfaces of leaves and soils; these organisms infiltrate into the indoor environment or may be transported into the building by people. Thus, fungi and bacteria are commonly found in indoor air and on the surfaces of floor, wall, and ceiling systems or on surfaces in air-handling equipment. When mold spores are present in large numbers, they can cause allergic reactions, asthma episodes, infections and other respiratory problems. Although proof of the connection between specific exposures and symptoms is often impossible to obtain, it is possible to demonstrate bioaerosol reservoirs, amplifiers, and disseminators during the inspection Individual susceptibility, the aforementioned factors do not affect all people equally: susceptibility varies with a range of factors such as atopy (predisposition to allergic sensitization), prior exposure, stress and gender. In some cases, the basis of the relationship is not clear. 1.2 SAMPLING METHODOLOGY Temperature and humidity were measured using the EXTECH Thermo-Hygrometer. Carbon dioxide was measured using a Telaire Carbon monoxide was measured using a MSA MiniCO Detector. Nitrogen dioxide, formaldehyde and ozone were measured using an MSA Kwik-Draw Pump detector tube. Total Petroleum Hydrocarbons 3

8 was measured using an Accuro Pump detector tube. Total nuisance dust was collected with a MIE personal DataRam (a real-time aerosol monitor). Biological, non-viable, total spore count samples were collected on Air-O-Cell cassettes at a flow rate of 10 liters per minute for approximately 10 minutes. The samples were sent to Environmental Laboratory Services (EM Lab) for identification. 2.0 RESULTS Table 2.1: The temperature and humidity and the CO, CO 2, formaldehyde, nitrogen oxides, ozone, total petroleum hydrocarbons and total dust sample results are listed below for the Non-Classroom Side Basement (10/11/17): CO CO 2 Total Dust TPH CHO NO 2 O 3 T/H Location (ppm) (ppm) (mg/m 3 ) (mg/m 3 ) (ppm) (ppm) (ppm) 0 f/% Mech Space/PTA BDL BDL BDL BDL 71/69 PTA Storage Room BDL BDL BDL BDL 71/69 Custodial Office BDL BDL BDL BDL 73/71 Outside # BDL BDL BDL BDL 71/63 Custodial Storage Rm BDL BDL BDL BDL 71/71 Outside # BDL BDL BDL BDL 71/63 Boiler Room BDL BDL BDL BDL 71/70 Note: BDL = below detectable limit; PPM = parts per million, F/CC = fibers per cubic meter, N/A = not applicable, pci = PicoCuries, NO 2 = nitrogen dioxide, CHO = formaldehyde, mg/m 2 = milligrams per cubic meter, TPH = total petroleum hydrocarbons Overall Uncertainty of detector tubes: NO 2 +/- 15%; O 3 +/- 25%; formaldehyde +/- 25%; TPH +/- 10%; Outside Sample #1 collected at basement entrance; Outside Sample #2 collected in the courtyard Table 2.2 Bioaerosol Samples (for details see the attached report dated 10/11/17 for the Non-Classroom Side Basement): MoldSCORE MoldSCORE Sample Conc. Compared to Compared to Location (spores/m 3 ) Outside Sample #1 Outside Sample #2 Mechanical Rm/PTA Storage PTA Storage Room Custodial Office Custodial Storage Room Boiler Room Outside #1 351,390 NA NA Outside # NA NA Note: CFU/M 3 = Colony-forming units per cubic meter; NA = not applicable; BDL = below detectable limit; Spores/M3 = spores per cubic meter; Outside Sample #1 collected at basement entrance; Outside Sample #2 collected in the courtyard 4

9 Table 2.3: The temperature and humidity and the CO, CO 2, formaldehyde, nitrogen oxides, ozone, total petroleum hydrocarbons and total dust sample results are listed below (10/28/17): CO CO 2 Total Dust TPH CHO NO 2 O 3 T/H Location (ppm) (ppm) (mg/m 3 ) (mg/m 3 ) (ppm) (ppm) (ppm) 0 f/% Main Office BDL BDL BDL BDL 56/51 Classroom BDL BDL BDL BDL 51/44 Classroom 2B BDL BDL BDL BDL 59/46 Cafeteria BDL BDL BDL BDL 55/43 Music Room BDL BDL BDL BDL 52/43 Classroom BDL BDL BDL BDL 57/48 Classroom BDL BDL BDL BDL 56/47 Classroom BDL BDL BDL BDL 57/46 Library BDL BDL BDL BDL 53/41 Computer Room BDL BDL BDL BDL 55/43 Classroom BDL BDL BDL BDL 55/47 Classroom BDL BDL BDL BDL 55/49 Classroom BDL BDL BDL BDL 55/43 Classroom BDL BDL BDL BDL 54/43 Classroom 9A BDL BDL BDL BDL 56/47 Classroom 8A BDL BDL BDL BDL 56/46 Nurse s Office BDL BDL BDL BDL 58/51 Classroom BDL BDL BDL BDL 56/47 Marker Space BDL BDL BDL BDL 58/52 Psychologist Office BDL BDL BDL BDL 58/50 Classroom 7A BDL BDL BDL BDL 58/53 Classroom BDL BDL BDL BDL 57/48 Classroom BDL BDL BDL BDL 57/49 Classroom BDL BDL BDL BDL 58/47 Gym # BDL BDL BDL BDL 59/65 Gym # BDL BDL BDL BDL 59/65 Classroom BDL BDL BDL BDL 54/43 Classroom BDL BDL BDL BDL 58/48 Classroom BDL BDL BDL BDL 56/45 Teacher s Lounge BDL BDL BDL BDL 56/48 Classroom 2A BDL BDL BDL BDL 59/46 Classroom BDL BDL BDL BDL 54/46 Classroom BDL BDL BDL BDL 54/52 Classroom BDL BDL BDL BDL 56/45 Classroom BDL BDL BDL BDL 58/53 Classroom BDL BDL BDL BDL 56/48 Art Room BDL BDL BDL BDL 57/48 Classroom BDL BDL BDL BDL 56/44 Outdoor # BDL BDL BDL BDL 56/46 Outdoor # BDL BDL BDL BDL 58/51 5

10 Note: BDL = below detectable limit; PPM = parts per million, F/CC = fibers per cubic meter, N/A = not applicable, pci = PicoCuries, NO 2 = nitrogen dioxide, CHO = formaldehyde, mg/m 2 = milligrams per cubic meter, TPH = total petroleum hydrocarbons Overall Uncertainty of detector tubes: NO 2 +/- 15%; O 3 +/- 25%; formaldehyde +/- 25%; TPH +/- 10% Table /28/17): Bioaerosol Samples (for details see the attached report dated MoldSCORE MoldSCORE Sample Conc. Compared to Compared to Location (spores/m 3 ) Outside Sample #1 Outside Sample #2 Main Office Classroom Classroom 2B Cafeteria Music Room Classroom Classroom Classroom Library Computer Room Classroom Classroom Classroom Classroom Classroom 9A Classroom 8A Nurse s Office Classroom Marker Space 50 Psychologist Office Classroom 7A Classroom Classroom Classroom Gym # Gym # Classroom Classroom Classroom Teacher s Lounge Classroom 2A Classroom Classroom Classroom Classroom Classroom MoldSCORE MoldSCORE 6

11 Sample Conc. Compared to Compared to Location (spores/m 3 ) Outside Sample #1 Outside Sample #2 Art Room Classroom Outdoor # NA NA Outdoor # NA NA Note: CFU/M 3 = Colony-forming units per cubic meter; NA = not applicable; BDL = below detectable limit; Spores/M3 = spores per cubic meter 3.0 OBSERVATIONS AND DISCUSSION 3.1 Carbon dioxide: The average indoor CO 2 concentration was greater than the outdoor concentration as is expected from occupied/previously occupied enclosed spaces and is not a health concern. The CO 2 levels were below the ASHRAE guidelines of 0 ppm. 3.2 Carbon monoxide: The average indoor CO concentration is equal to the outdoor concentration. 3.3 Nitrogen dioxide: The average indoor NO 2 concentration is below or equal to the comparison sample and the outdoor concentration. No standards have been agreed upon for nitrogen dioxides in indoor air. ASHRAE and the EPA National Ambient Air Quality Standards list ppm as the average 24-hour limit for NO 2 in outdoor air. 3.4 Ozone: The average indoor O 3 concentration is below or equal to the comparison sample and the outdoor concentration. Maximum allowable ozone concentration recommended by ASHRAE in an air conditioned and ventilated space to ppm. 3.5 Formaldehyde: The average indoor formaldehyde concentration is below or equal to the comparison sample and the outdoor concentration. 3.6 Total Petroleum Hydrocarbons: The average indoor total petroleum hydrocarbons concentration is equal to the non-compliant area and the outdoor concentration. There is no OSHA standard for the amount of petroleum oil vapors allowed in homes or workplaces. Most people can smell oil vapors at levels as low as 0.1 parts per million (ppm) in air. 3.7 Total nuisance dust: The average indoor total dust concentration is below or equal to the comparison sample and the outdoor concentration. 3.8 Temperature and Humidity: Humidity, like temperature exerts a powerful effect on building inhabitants. The direct consequence of high humidity is discomfort. Highly saturated warm air reduces the body s ability to lose heat and can increase levels of body odors. The chief problem with high indoor humidity from a health standpoint is the 7

12 potential for mold growth. Humidity levels greater than 30% increase the potential for mold growth and high humidity, 60% or greater can cause biological contamination. Dry air can affect the human body by causing respiratory ailments such as asthma, bronchitis, sinusitis, and nosebleeds, or general dehydration since the body fluids are depleted during respiration. Skin moisture evaporation can cause skin irritations and eye itching and the apparent temperature of the air is lower than what the thermometer indicates and the body feels colder. The humidity level in the building is typical of building without mechanical ventilation during the autumn months. Recommended Ranges of Temperature and Relative Humidity Relative Winter Summer Humidity Temperature Temperature 30% 68.5 o F 75.5 o F 74.0 o F 80.0 o F 40% 68.0 o F 75.0 o F 73.5 o F 80.0 o F 50% 68.0 o F 74.5 o F 73.0 o F 79.0 o F 60% 67.5 o F 74.0 o F 73.0 o F 78.5 o F 3.9 Bioaerosols: Samples were collected from selected areas in the building and an outside sample was collected to determine the organisms that occupy the ambient air (mycoflora) at the time of the investigation. Because there can be such variation in spore trap samples the statistical significance from collecting few samples is very limited and no single particulate sample is representative of any environment (the particles are never randomly distributed in the space, especially when the particles are bioaerosols), therefore, two (2) outdoor air samples were collected. Two outdoor air samples will help provide a more complete picture of what is in the air that may be entering the building through windows and doors at times when they are open. Samples were collected in pre-identified areas in the building. The organisms identified in the majority of the indoor air samples collected are typically those found in the air from the exterior of the building and no action is required. The non-classroom side of the basement had a MoldSCORE that ranged from Outside sample #1 was collected in the outside stairwell from the courtyard to the basement. The stairwell is littered with leaves and the floor drain is clogged. The MoldSCORE is higher in the stairwell then the courtyard where outside sample #2 was collected, and it is assumed that there is mold growth occurring in the leaf litter on the stairwell floor. The custodial staff routinely open the door to allow outside air to enter the basement where their office is located. There was visual evidence of mold growth in the basement boiler room. The MoldSCORE along with visual observations have concluded that fungal growth has occurred in the basement boiler room. A MoldSCORE rating greater than 150 indicates a moderate probability that the spores originated from inside the building and greater than 250 indicates a high probability. 8

13 The organisms identified in the indoor air samples collected in the Psychologist Office, classroom 7A and room 9, had a MoldSCORE range from , consisting of Smuts, Periconia and Myxomycetes, which are typically outdoor organism/plant pathogens. The MoldSCORE for these classrooms is an artificiality and can occur when specific spore types are high outdoors and infiltrate into a building on a certain day (as does pollen) but remain indoors and then exceed outdoor levels that have subsequently decreased. This can be and is commonly seen with obligate plant parasites, such as rust fungi or tree pathogens that never colonize indoor spaces, yet can occur indoors in excess of outdoor levels on given days. Therefore, the organisms identified in the indoor air samples are those found in the air from the exterior of the building and no action is required. The organism identified in classroom 2B, classroom 22, classroom 35 and the Teacher s Lounge had a MoldScore range from , which indicates that there is a moderate probability that the spores originated inside the rooms. Mold growth was visually identified in the Teacher s Lounge, beneath the contact paper in the cabinet beneath the sink. Bioaerosol sampling only represents a snap shot in time and the true average concentration of microorganisms may differ. Molds are part of the natural environment, and can be found everywhere, indoors and outdoors. They are found in schools, homes, hospitals, industry etc. Outdoors, molds play a part in nature by breaking down dead organic matter such as fallen leaves and dead trees. It is impossible to get rid of all mold and mold spores indoors; some mold spores will be found floating through the air and in house/school dust. However, mold is not usually a problem, unless it begins growing indoors and not appropriately corrected. Mold exposure can irritate the eyes, skin, nose, throat, and lungs of both mold-allergic and non-allergic people. Symptoms other than the allergic and irritant types are not commonly reported as a result of inhaling mold. The bioaerosol results for Greenacres School are typical of findings that RegCom has identified in other public schools, hospitals etc. over the past 20 years. Greenacres school has a few isolated areas that need attention or further investigation if recommended actions fail to correct the situation. The presence of fungi in the air does not necessitate that people will be or exhibit health effects. In order for humans to be exposed indoors, fungal spores, fragments, or metabolites must be released into the air and inhaled, physically contacted (dermal exposure), or ingested. Whether or not symptoms develop in people exposed to fungi depends on the nature of the fungal material (e.g., allergenic, toxic, or infectious), the amount of exposure, and the susceptibility of exposed persons. Susceptibility varies with the genetic predisposition (e.g., allergic reactions do not always occur in all individuals), age, state of health, and concurrent exposures. For this reason and because measurements are not standardized and biological markers of exposures to fungi are largely unknown, it is not possible to determine a safe or unsafe levels of exposure for people in general. Science there is no biological concentration standards or permissible exposure limits (PELs) against which to compare a particular bioaerosol result, we are forced to use several tools to assist in the interpretation of the bioaerosol results. 9

14 The current approach relies on the comparisons of indoor vs. outdoor results and complaint vs. non-complaint area results. 1. Indoor levels that are below outdoor levels are usually not a concern, unless the speciazation identifies an opportunistic pathogen. 2. Compare the total concentrations form indoor, outdoor, complaint and noncomplaint areas. Indoor levels may be greater than the exterior sample concentration (a concentration effect might be occurring or the outdoor environmental conditions may be prohibiting reproduction or removing the spores from the air). 3. Compare fungal genera and species, similar genera and species should be present in the exterior and interior samples, complaint and non-complaint samples. Another tool that was developed by EM Laboratory Inc, is a proprietary statistical calculation called a MoldSCORE TM. The MoldSCORE TM is a specliazed method for examining air-sampling spore data only data. The statistical valves lay between and 300, the lower the score the greater the likihood that the indoor spores originated from the outdoors. The organisms identified in the indoor air samples are typically those found in the air from the exterior of the building. The MoldSCORE TM. suggest that the mold identified in the areas surveyed is from an exterior source. It must be noted that these numerical values are only an assumption based on experience and scientific literature. The numbers are artificial and should not be used as a health and safety standard. It should also be noted, that rather than focusing on specific kinds of fungi or on quantitative measurements of fungal prevalence, the ACGIH approach has been to emphasize that actual fungal growth in indoor environments is inappropriate and may lead to exposure and adverse health affect Carpets, throw rugs and upholstery (throw cushions): Carpets are generally used in the classroom or hallways to reduce the noise levels or to create a softer walking surface and throw rugs are commonly used in classrooms to crate a soft-sitting surface for younger students. However, carpets and throw rugs require maintenance and they do not clean as well as hard non-porus surfaces (floor tile). These fleecy materials become sinks or reservoirs where microorganisms accumulate (dust mites, bacteria and mold). If this material becomes wet and does not dry within 48 hours or if an object is placed on a wet carpet, preventing it from drying, fungus and bacterial will grow. Cleaning a carpet with fungal growth is difficult to accomplish and therefore, removal is usually the best option. Therefore, it is important that the throw carpet and pillows be periodically removed and cleaned. If occupants of the classroom develop an allergy the practice of using carpet and/or cushions should be discontinued Asthma: A number of occupants openly indicted that they were either asthmatic or suffered from allergies or other respiratory illness. Americans spend up to 90% of their time indoors. Therefore, indoor allergens and irritants can play a significant role in triggering asthma attacks. Some of the most common indoor asthma triggers include 10

15 secondhand smoke, dust mites, mold, cockroaches and other pests, household pets, and combustion byproducts Building Inspection: Internal Building Inspection: The affected rooms were inspected and appeared to be dry, with the exception of minor water intrusion in the boiler room area. The mechanical room next to the PTA storage room has an active sump pump. Overall, the basement is used as a storage and shop area, custodial office space and the boiler room. The basement is below grade and isolated from the remainder of the basement. The is a portion of the basement that is student occupied (classrooms) was found to be clean and dry. The other areas of the building that were inspected also found to be clean and dry with the exception of water damaged cabinet floor beneath the sink in rooms 2B and 35. There is communication between the crawl space, the kiln room and the art room through the hatch way door opening. Air was moving from the crawl space into the classroom. 4.0 CONCLUSION The MoldSCORE along with visual observations have concluded that fungal growth was occurring in the boiler room in the basement and in the Teacher s Lounge. There are a number of areas where the MoldSCORE indicate that there is a moderate probability that the spore originated interior to the building. The average concentration for nuisance dust, formaldehyde, ozone, nitrogen dioxide carbon monoxide, carbon dioxide and total petroleum hydrocarbons were below or equal to the outside sample. None of the information contained herein should be construed as medical advice. Only a qualified physician should make any decision relative to medical significance. 5.0 RECOMMENDATIONS Basement (non-classroom areas): 1. Inspect and remove material that appears moldy, this includes wood, paper products etc. 2. Clean and disinfect the areas. 3. Remove debris an ensure floor drain is working properly in the courtyard basement stairwell. 4. Install dehumidifiers, if humidity can t be controlled. 5. Ensure areas where sump pumps are located are ventilated to the outside. 11

16 6. Ventilate the basement (non-classroom areas). 7. Seal penetrations between the basement and the first floor. 8. Inspect the area for water intrusion and correct if identified. Classroom 35, 22, 2B and the Teacher s Lounge: 1. Inspect and remove material that appears moldy, this includes wood, paper products etc. 2. Clean and disinfect the areas. 3. Install dehumidifiers, if humidity can t be controlled. 4. Inspect the area for water intrusion and correct if identified. 5. Inspect and clean window AC units. 6. Clean and disinfect the cabinets beneath the sink and replace cabinet floors beneath the sinks as needed. 7. Clean and disinfect the ventilation grills. 8. Inspect and clean unit ventilators/replace filters as needed. 9. Seal the penetration (floor hatch) to the crawl space in the Art room/kiln room. 12

17 Microbiological Sample Results 13

18 Report for: Mr. Ernest Coon Regulatory Compliance 245 Albany Ave Thornwood, NY Regarding: Project: SCAR IAQ EML ID: Approved by: Dates of Analysis: Spore trap analysis: Technical Manager Francina Thadigiri Service SOPs: Spore trap analysis (EM-MY-S-1038) AIHA-LAP, LLC accredited service, Lab ID # All samples were received in acceptable condition unless noted in the Report Comments portion in the body of the report. Due to the nature of the analyses performed, field blank correction of results is not applied. The results relate only to the items tested. ("the Company") shall have no liability to the client or the client's customer with respect to decisions or recommendations made, actions taken or courses of conduct implemented by either the client or the client's customer as a result of or based upon the Test Results. In no event shall the Company be liable to the client with respect to the Test Results except for the Company's own willful misconduct or gross negligence nor shall the Company be liable for incidental or consequential damages or lost profits or revenues to the fullest extent such liability may be disclaimed by law, even if the Company has been advised of the possibility of such damages, lost profits or lost revenues. In no event shall the Company's liability with respect to the Test Results exceed the amount paid to the Company by the client therefor. 's LabServe reporting system includes automated fail-safes to ensure that all AIHA-LAP, LLC quality requirements are met and notifications are added to reports when any quality steps remain pending. EMLab ID: , Page 1 of 21

19 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Main office : Room 4 Comments (see below) None None Lab ID-Version : Analysis Date: 11/01/ /01/2017 raw ct. % read spores/m3 raw ct. % read spores/m3 Alternaria Ascospores Basidiospores Bipolaris/Drechslera group 1 10 Botrytis Cercospora Chaetomium Cladosporium Curvularia 1 10 Epicoccum Fusarium Other brown 1 10 Penicillium/Aspergillus types Pestalotiopsis Pithomyces Polythrincium Rusts Smuts, Periconia, Myxomycetes 1 10 Stachybotrys 1 10 Tetraploa Background debris (1-4+) Hyphal fragments/m Pollen/m3 < Skin cells (1-4+) < Sample volume (liters) TOTAL SPORES/m Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 2 of 21

20 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Room 2b : Cafeteria Comments (see below) A None Lab ID-Version : Analysis Date: 11/01/ /01/2017 raw ct. % read spores/m3 raw ct. % read spores/m3 Alternaria Ascospores Basidiospores Bipolaris/Drechslera group Botrytis Cercospora Chaetomium Cladosporium Curvularia Epicoccum 1 10 Fusarium Other brown Penicillium/Aspergillus types 27/12 25/ 1, Pestalotiopsis Pithomyces 1 10 Polythrincium Rusts 1 10 Smuts, Periconia, Myxomycetes Stachybotrys Tetraploa Background debris (1-4+) Hyphal fragments/m Pollen/m3 < 10 < 10 Skin cells (1-4+) 1+ < 1+ Sample volume (liters) TOTAL SPORES/m3 1, Comments:A) 12 of the raw count Penicillium/Aspergillus type spores were present as a single clump. Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 3 of 21

21 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Music Room : Room 20 Comments (see below) None None Lab ID-Version : Analysis Date: 11/01/ /01/2017 raw ct. % read spores/m3 raw ct. % read spores/m3 Alternaria 1 10 Ascospores Basidiospores Bipolaris/Drechslera group Botrytis 2 20 Cercospora Chaetomium Cladosporium Curvularia 1 10 Epicoccum 1 10 Fusarium Other brown 2 20 Penicillium/Aspergillus types Pestalotiopsis Pithomyces Polythrincium Rusts Smuts, Periconia, Myxomycetes Stachybotrys Tetraploa Background debris (1-4+) Hyphal fragments/m3 < Pollen/m3 < 10 < 10 Skin cells (1-4+) < 1+ < 1+ Sample volume (liters) TOTAL SPORES/m Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 4 of 21

22 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Room : Room 18 Comments (see below) None None Lab ID-Version : Analysis Date: 11/01/ /01/2017 raw ct. % read spores/m3 raw ct. % read spores/m3 Alternaria Ascospores Basidiospores Bipolaris/Drechslera group Botrytis Cercospora Chaetomium Cladosporium Curvularia Epicoccum Fusarium Other brown Penicillium/Aspergillus types Pestalotiopsis Pithomyces Polythrincium Rusts Smuts, Periconia, Myxomycetes 5 50 Stachybotrys Tetraploa Background debris (1-4+) Hyphal fragments/m Pollen/m3 < 10 < 10 Skin cells (1-4+) < 1+ < 1+ Sample volume (liters) TOTAL SPORES/m Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 5 of 21

23 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Library : Computer room Comments (see below) None None Lab ID-Version : Analysis Date: 11/01/ /01/2017 raw ct. % read spores/m3 raw ct. % read spores/m3 Alternaria Ascospores Basidiospores Bipolaris/Drechslera group Botrytis Cercospora Chaetomium Cladosporium Curvularia Epicoccum Fusarium Other brown 1 10 Penicillium/Aspergillus types Pestalotiopsis 1 10 Pithomyces 1 10 Polythrincium Rusts 1 10 Smuts, Periconia, Myxomycetes Stachybotrys Tetraploa Background debris (1-4+) Hyphal fragments/m3 < 10 < 10 Pollen/m3 < 10 < 10 Skin cells (1-4+) < Sample volume (liters) TOTAL SPORES/m Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 6 of 21

24 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Room : Room 12 Comments (see below) None None Lab ID-Version : Analysis Date: 11/01/ /01/2017 raw ct. % read spores/m3 raw ct. % read spores/m3 Alternaria 1 10 Ascospores Basidiospores Bipolaris/Drechslera group Botrytis Cercospora Chaetomium Cladosporium Curvularia 1 10 Epicoccum Fusarium Other brown 1 10 Penicillium/Aspergillus types Pestalotiopsis 1 10 Pithomyces Polythrincium Rusts 1 10 Smuts, Periconia, Myxomycetes Stachybotrys Tetraploa 1 10 Background debris (1-4+) Hyphal fragments/m Pollen/m3 < 10 < 10 Skin cells (1-4+) < 1+ < 1+ Sample volume (liters) TOTAL SPORES/m Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 7 of 21

25 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Room : Room 10 Comments (see below) None None Lab ID-Version : Analysis Date: 11/01/ /01/2017 raw ct. % read spores/m3 raw ct. % read spores/m3 Alternaria Ascospores Basidiospores Bipolaris/Drechslera group Botrytis Cercospora Chaetomium Cladosporium Curvularia 1 10 Epicoccum 1 10 Fusarium Other brown Penicillium/Aspergillus types Pestalotiopsis Pithomyces 2 20 Polythrincium Rusts Smuts, Periconia, Myxomycetes Stachybotrys Tetraploa Background debris (1-4+) Hyphal fragments/m Pollen/m3 < 10 < 10 Skin cells (1-4+) < 1+ < 1+ Sample volume (liters) TOTAL SPORES/m Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 8 of 21

26 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Room 9A : Room 8A Comments (see below) None B Lab ID-Version : Analysis Date: 11/01/ /01/2017 raw ct. % read spores/m3 raw ct. % read spores/m3 Alternaria 1 10 Ascospores Basidiospores Bipolaris/Drechslera group Botrytis Cercospora Chaetomium Cladosporium /6 25/ Curvularia Epicoccum Fusarium Other brown Penicillium/Aspergillus types Pestalotiopsis 1 10 Pithomyces Polythrincium Rusts 1 10 Smuts, Periconia, Myxomycetes 1 10 Stachybotrys Tetraploa Background debris (1-4+) Hyphal fragments/m Pollen/m3 < 10 < 10 Skin cells (1-4+) < 1+ < 1+ Sample volume (liters) TOTAL SPORES/m Comments:B) 6 of the raw count Cladosporium spores were present as a single clump. Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 9 of 21

27 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Nurses office : Room 35 Comments (see below) None None Lab ID-Version : Analysis Date: 11/01/ /01/2017 raw ct. % read spores/m3 raw ct. % read spores/m3 Alternaria 2 20 Ascospores Basidiospores Bipolaris/Drechslera group Botrytis Cercospora Chaetomium Cladosporium Curvularia 1 10 Epicoccum Fusarium Other brown 3 30 Penicillium/Aspergillus types Pestalotiopsis 1 10 Pithomyces 3 30 Polythrincium Rusts 1 10 Smuts, Periconia, Myxomycetes Stachybotrys Tetraploa Background debris (1-4+) Hyphal fragments/m Pollen/m3 < 10 < 10 Skin cells (1-4+) < 1+ < 1+ Sample volume (liters) TOTAL SPORES/m ,000 Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 10 of 21

28 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Outdoor sample # : Outdoor sample #2 Comments (see below) None None Lab ID-Version : Analysis Date: 11/01/ /01/2017 raw ct. % read spores/m3 raw ct. % read spores/m3 Alternaria Ascospores Basidiospores , ,700 Bipolaris/Drechslera group Botrytis Cercospora 1 10 Chaetomium Cladosporium ,700 Curvularia Epicoccum 2 20 Fusarium 1 10 Other brown Penicillium/Aspergillus types Pestalotiopsis 3 30 Pithomyces Polythrincium 2 20 Rusts Smuts, Periconia, Myxomycetes Stachybotrys Tetraploa Background debris (1-4+) Hyphal fragments/m3 110 < 10 Pollen/m3 < 10 < 10 Skin cells (1-4+) < 1+ < 1+ Sample volume (liters) TOTAL SPORES/m3 3,000 11,000 Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 11 of 21

29 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Maker space : Psych office Comments (see below) None None Lab ID-Version : Analysis Date: 11/01/ /01/2017 raw ct. % read spores/m3 raw ct. % read spores/m3 Alternaria 1 10 Ascospores Basidiospores Bipolaris/Drechslera group 1 10 Botrytis Cercospora Chaetomium Cladosporium Curvularia Epicoccum Fusarium Other brown Penicillium/Aspergillus types Pestalotiopsis Pithomyces 5 50 Polythrincium Rusts 2 20 Smuts, Periconia, Myxomycetes Stachybotrys Tetraploa Background debris (1-4+) Hyphal fragments/m3 < 10 Pollen/m3 < 10 < 10 Skin cells (1-4+) < 1+ < 1+ Sample volume (liters) TOTAL SPORES/m Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 12 of 21

30 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Room 7A : Room 8 Comments (see below) None None Lab ID-Version : Analysis Date: 11/01/ /01/2017 raw ct. % read spores/m3 raw ct. % read spores/m3 Alternaria Ascospores Basidiospores Bipolaris/Drechslera group Botrytis Cercospora Chaetomium Cladosporium Curvularia 5 50 Epicoccum 2 20 Fusarium Other brown 2 20 Penicillium/Aspergillus types Pestalotiopsis Pithomyces Polythrincium Rusts Smuts, Periconia, Myxomycetes Stachybotrys Torula 1 10 Background debris (1-4+) Hyphal fragments/m Pollen/m3 30 < 10 Skin cells (1-4+) 1+ < 1+ Sample volume (liters) TOTAL SPORES/m Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 13 of 21

31 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Room : Room 25 Comments (see below) None None Lab ID-Version : Analysis Date: 11/01/ /01/2017 raw ct. % read spores/m3 raw ct. % read spores/m3 Alternaria 1 10 Ascospores Basidiospores Bipolaris/Drechslera group Botrytis Cercospora Chaetomium Cladosporium Curvularia 2 20 Epicoccum 1 10 Fusarium Other brown 1 10 Penicillium/Aspergillus types Pestalotiopsis 1 10 Pithomyces 1 10 Polythrincium Rusts 2 20 Smuts, Periconia, Myxomycetes Stachybotrys Tetraploa Background debris (1-4+) Hyphal fragments/m Pollen/m Skin cells (1-4+) < 1+ < 1+ Sample volume (liters) TOTAL SPORES/m Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 14 of 21

32 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Gym : Gym sample 2 Comments (see below) None None Lab ID-Version : Analysis Date: 11/01/ /01/2017 raw ct. % read spores/m3 raw ct. % read spores/m3 Alternaria Ascospores Basidiospores Bipolaris/Drechslera group Botrytis Cercospora Chaetomium Cladosporium Curvularia Epicoccum Fusarium Other brown 1 10 Penicillium/Aspergillus types Pestalotiopsis Pithomyces 1 10 Polythrincium Rusts 1 10 Smuts, Periconia, Myxomycetes Stachybotrys 2 20 Tetraploa Background debris (1-4+) Hyphal fragments/m Pollen/m3 < 10 < 10 Skin cells (1-4+) < 1+ < 1+ Sample volume (liters) TOTAL SPORES/m Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 15 of 21

33 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Room : Room 22 Comments (see below) None None Lab ID-Version : Analysis Date: 11/01/ /01/2017 raw ct. % read spores/m3 raw ct. % read spores/m3 Alternaria 2 20 Ascospores Basidiospores Bipolaris/Drechslera group Botrytis Cercospora Chaetomium Cladosporium Curvularia Epicoccum Fusarium Other brown 1 10 Penicillium/Aspergillus types Pestalotiopsis Pithomyces 4 40 Polythrincium Rusts Smuts, Periconia, Myxomycetes Stachybotrys 1 10 Tetraploa Background debris (1-4+) Hyphal fragments/m Pollen/m3 < Skin cells (1-4+) < Sample volume (liters) TOTAL SPORES/m Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 16 of 21

34 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Room : Teachers lounge Comments (see below) None C Lab ID-Version : Analysis Date: 11/01/ /01/2017 raw ct. % read spores/m3 raw ct. % read spores/m3 Alternaria 1 10 Ascospores Basidiospores Bipolaris/Drechslera group Botrytis Cercospora Chaetomium Cladosporium Curvularia Epicoccum Fusarium Other brown Penicillium/Aspergillus types /120 25/ 1,200 Pestalotiopsis Pithomyces 1 10 Polythrincium 1 10 Rusts 1 10 Smuts, Periconia, Myxomycetes 2 20 Stachybotrys Tetraploa Background debris (1-4+) Hyphal fragments/m3 < Pollen/m Skin cells (1-4+) < Sample volume (liters) TOTAL SPORES/m ,400 Comments:C) 120 of the raw count Penicillium/Aspergillus type spores were present as a single clump. Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 17 of 21

35 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Room 2A : Room 5 Comments (see below) None None Lab ID-Version : Analysis Date: 11/01/ /01/2017 raw ct. % read spores/m3 raw ct. % read spores/m3 Alternaria Ascospores Basidiospores Bipolaris/Drechslera group Botrytis Cercospora Chaetomium Cladosporium Curvularia Epicoccum 1 10 Fusarium Other brown 1 10 Penicillium/Aspergillus types Pestalotiopsis Pithomyces 1 10 Polythrincium Rusts Smuts, Periconia, Myxomycetes 2 20 Stachybotrys Tetraploa Background debris (1-4+) Hyphal fragments/m3 < 10 < 10 Pollen/m3 < 10 < 10 Skin cells (1-4+) < 1+ < 1+ Sample volume (liters) TOTAL SPORES/m Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 18 of 21

36 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Room : Room 9 Comments (see below) None None Lab ID-Version : Analysis Date: 11/01/ /01/2017 raw ct. % read spores/m3 raw ct. % read spores/m3 Alternaria Ascospores Basidiospores Bipolaris/Drechslera group Botrytis Cercospora Chaetomium Cladosporium Curvularia 1 10 Epicoccum 2 20 Fusarium Other brown Penicillium/Aspergillus types Pestalotiopsis Pithomyces 2 20 Polythrincium Rusts 3 30 Smuts, Periconia, Myxomycetes Stachybotrys 1 10 Tetraploa Background debris (1-4+) Hyphal fragments/m3 < 10 < 10 Pollen/m3 < 10 < 10 Skin cells (1-4+) < Sample volume (liters) TOTAL SPORES/m Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 19 of 21

37 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Room : Room 23 Comments (see below) None None Lab ID-Version : Analysis Date: 11/01/ /01/2017 raw ct. % read spores/m3 raw ct. % read spores/m3 Alternaria 1 10 Ascospores Basidiospores Bipolaris/Drechslera group Botrytis Cercospora Chaetomium Cladosporium Curvularia 1 10 Epicoccum Fusarium Other brown 2 20 Penicillium/Aspergillus types Pestalotiopsis Pithomyces Polythrincium Rusts 1 10 Smuts, Periconia, Myxomycetes Stachybotrys Tetraploa Background debris (1-4+) Hyphal fragments/m3 < 10 < 10 Pollen/m Skin cells (1-4+) < Sample volume (liters) TOTAL SPORES/m Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 20 of 21

38 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Art Room : Room 34 Comments (see below) None None Lab ID-Version : Analysis Date: 11/01/ /01/2017 raw ct. % read spores/m3 raw ct. % read spores/m3 Alternaria 1 10 Ascospores Basidiospores Bipolaris/Drechslera group Botrytis Cercospora Chaetomium Cladosporium Curvularia Epicoccum Fusarium Other brown Penicillium/Aspergillus types Pestalotiopsis Pithomyces 1 10 Polythrincium Rusts 1 10 Smuts, Periconia, Myxomycetes Stachybotrys Tetraploa Background debris (1-4+) Hyphal fragments/m3 10 < 10 Pollen/m3 10 < 10 Skin cells (1-4+) < 1+ < 1+ Sample volume (liters) TOTAL SPORES/m Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 21 of 21

39 Report for: Mr. Ernest Coon Regulatory Compliance 245 Albany Ave Thornwood, NY Regarding: Project: SCAR IAQ EML ID: Approved by: Dates of Analysis: Spore trap analysis: Technical Manager Francina Thadigiri Service SOPs: Spore trap analysis (EM-MY-S-1038) AIHA-LAP, LLC accredited service, Lab ID # All samples were received in acceptable condition unless noted in the Report Comments portion in the body of the report. Due to the nature of the analyses performed, field blank correction of results is not applied. The results relate only to the items tested. ("the Company") shall have no liability to the client or the client's customer with respect to decisions or recommendations made, actions taken or courses of conduct implemented by either the client or the client's customer as a result of or based upon the Test Results. In no event shall the Company be liable to the client with respect to the Test Results except for the Company's own willful misconduct or gross negligence nor shall the Company be liable for incidental or consequential damages or lost profits or revenues to the fullest extent such liability may be disclaimed by law, even if the Company has been advised of the possibility of such damages, lost profits or lost revenues. In no event shall the Company's liability with respect to the Test Results exceed the amount paid to the Company by the client therefor. 's LabServe reporting system includes automated fail-safes to ensure that all AIHA-LAP, LLC quality requirements are met and notifications are added to reports when any quality steps remain pending. EMLab ID: , Page 1 of 11

40 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Main office : Room : Room 2b : Cafeteria Comments (see below) None None A None Lab ID-Version : Analysis Date: 11/01/ /01/ /01/ /01/2017 raw ct. spores/m3 raw ct. spores/m3 raw ct. spores/m3 raw ct. spores/m3 Alternaria Ascospores Basidiospores Bipolaris/Drechslera group 1 10 Botrytis Cercospora Chaetomium Cladosporium Curvularia 1 10 Epicoccum 1 10 Fusarium Other brown Penicillium/Aspergillus types , Pestalotiopsis Pithomyces Polythrincium Rusts 1 10 Smuts, Periconia, Myxomycetes Stachybotrys 1 10 Tetraploa Torula Background debris (1-4+) Hyphal fragments/m Pollen/m3 < < 10 < 10 Skin cells (1-4+) < < 1+ Sample volume (liters) TOTAL SPORES/m , Comments:A) 12 of the raw count Penicillium/Aspergillus type spores were present as a single clump. Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 2 of 11

41 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Music Room : Room : Room : Room 18 Comments (see below) None None None None Lab ID-Version : Analysis Date: 11/01/ /01/ /01/ /01/2017 raw ct. spores/m3 raw ct. spores/m3 raw ct. spores/m3 raw ct. spores/m3 Alternaria 1 10 Ascospores Basidiospores Bipolaris/Drechslera group Botrytis 2 20 Cercospora Chaetomium Cladosporium Curvularia 1 10 Epicoccum 1 10 Fusarium Other brown 2 20 Penicillium/Aspergillus types Pestalotiopsis Pithomyces Polythrincium Rusts Smuts, Periconia, Myxomycetes Stachybotrys Tetraploa Torula Background debris (1-4+) Hyphal fragments/m3 < Pollen/m3 < 10 < 10 < 10 < 10 Skin cells (1-4+) < 1+ < 1+ < 1+ < 1+ Sample volume (liters) TOTAL SPORES/m Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 3 of 11

42 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Library : Computer room : Room : Room 12 Comments (see below) None None None None Lab ID-Version : Analysis Date: 11/01/ /01/ /01/ /01/2017 raw ct. spores/m3 raw ct. spores/m3 raw ct. spores/m3 raw ct. spores/m3 Alternaria 1 10 Ascospores Basidiospores Bipolaris/Drechslera group Botrytis Cercospora Chaetomium Cladosporium Curvularia 1 10 Epicoccum Fusarium Other brown Penicillium/Aspergillus types Pestalotiopsis Pithomyces Polythrincium Rusts Smuts, Periconia, Myxomycetes Stachybotrys Tetraploa 1 10 Torula Background debris (1-4+) Hyphal fragments/m3 < 10 < Pollen/m3 < 10 < 10 < 10 < 10 Skin cells (1-4+) < < 1+ < 1+ Sample volume (liters) TOTAL SPORES/m Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 4 of 11

43 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Room : Room : Room 9A : Room 8A Comments (see below) None None None B Lab ID-Version : Analysis Date: 11/01/ /01/ /01/ /01/2017 raw ct. spores/m3 raw ct. spores/m3 raw ct. spores/m3 raw ct. spores/m3 Alternaria 1 10 Ascospores Basidiospores Bipolaris/Drechslera group Botrytis Cercospora Chaetomium Cladosporium Curvularia 1 10 Epicoccum 1 10 Fusarium Other brown Penicillium/Aspergillus types Pestalotiopsis 1 10 Pithomyces 2 20 Polythrincium Rusts 1 10 Smuts, Periconia, Myxomycetes Stachybotrys Tetraploa Torula Background debris (1-4+) Hyphal fragments/m Pollen/m3 < 10 < 10 < 10 < 10 Skin cells (1-4+) < 1+ < 1+ < 1+ < 1+ Sample volume (liters) TOTAL SPORES/m Comments:B) 6 of the raw count Cladosporium spores were present as a single clump. Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 5 of 11

44 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Nurses office : Room : Outdoor sample # : Outdoor sample #2 Comments (see below) None None None None Lab ID-Version : Analysis Date: 11/01/ /01/ /01/ /01/2017 raw ct. spores/m3 raw ct. spores/m3 raw ct. spores/m3 raw ct. spores/m3 Alternaria Ascospores Basidiospores , ,700 Bipolaris/Drechslera group Botrytis Cercospora 1 10 Chaetomium Cladosporium ,700 Curvularia Epicoccum 2 20 Fusarium 1 10 Other brown Penicillium/Aspergillus types Pestalotiopsis Pithomyces Polythrincium 2 20 Rusts Smuts, Periconia, Myxomycetes Stachybotrys Tetraploa Torula Background debris (1-4+) Hyphal fragments/m < 10 Pollen/m3 < 10 < 10 < 10 < 10 Skin cells (1-4+) < 1+ < 1+ < 1+ < 1+ Sample volume (liters) TOTAL SPORES/m ,000 3,000 11,000 Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 6 of 11

45 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Maker space : Psych office : Room 7A : Room 8 Comments (see below) None None None None Lab ID-Version : Analysis Date: 11/01/ /01/ /01/ /01/2017 raw ct. spores/m3 raw ct. spores/m3 raw ct. spores/m3 raw ct. spores/m3 Alternaria 1 10 Ascospores 1 40 Basidiospores 2 80 Bipolaris/Drechslera group 1 10 Botrytis Cercospora Chaetomium Cladosporium Curvularia 5 50 Epicoccum 2 20 Fusarium Other brown Penicillium/Aspergillus types Pestalotiopsis Pithomyces Polythrincium Rusts Smuts, Periconia, Myxomycetes Stachybotrys Tetraploa Torula 1 10 Background debris (1-4+) Hyphal fragments/m3 < Pollen/m3 < 10 < < 10 Skin cells (1-4+) < 1+ < < 1+ Sample volume (liters) TOTAL SPORES/m Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 7 of 11

46 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Room : Room : Gym : Gym sample 2 Comments (see below) None None None None Lab ID-Version : Analysis Date: 11/01/ /01/ /01/ /01/2017 raw ct. spores/m3 raw ct. spores/m3 raw ct. spores/m3 raw ct. spores/m3 Alternaria 1 10 Ascospores 1 40 Basidiospores Bipolaris/Drechslera group Botrytis Cercospora Chaetomium Cladosporium Curvularia 2 20 Epicoccum 1 10 Fusarium Other brown Penicillium/Aspergillus types Pestalotiopsis 1 10 Pithomyces Polythrincium Rusts Smuts, Periconia, Myxomycetes Stachybotrys 2 20 Tetraploa Torula Background debris (1-4+) Hyphal fragments/m Pollen/m < 10 < 10 Skin cells (1-4+) < 1+ < 1+ < 1+ < 1+ Sample volume (liters) TOTAL SPORES/m Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 8 of 11

47 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Room : Room : Room : Teachers lounge Comments (see below) None None None C Lab ID-Version : Analysis Date: 11/01/ /01/ /01/ /01/2017 raw ct. spores/m3 raw ct. spores/m3 raw ct. spores/m3 raw ct. spores/m3 Alternaria Ascospores Basidiospores Bipolaris/Drechslera group Botrytis Cercospora Chaetomium Cladosporium Curvularia Epicoccum Fusarium Other brown 1 10 Penicillium/Aspergillus types ,200 Pestalotiopsis Pithomyces Polythrincium 1 10 Rusts 1 10 Smuts, Periconia, Myxomycetes Stachybotrys 1 10 Tetraploa Torula Background debris (1-4+) Hyphal fragments/m < Pollen/m3 < Skin cells (1-4+) < < Sample volume (liters) TOTAL SPORES/m ,400 Comments:C) 120 of the raw count Penicillium/Aspergillus type spores were present as a single clump. Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 9 of 11

48 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Room 2A : Room : Room : Room 9 Comments (see below) None None None None Lab ID-Version : Analysis Date: 11/01/ /01/ /01/ /01/2017 raw ct. spores/m3 raw ct. spores/m3 raw ct. spores/m3 raw ct. spores/m3 Alternaria Ascospores 1 40 Basidiospores Bipolaris/Drechslera group Botrytis Cercospora Chaetomium Cladosporium Curvularia 1 10 Epicoccum Fusarium Other brown Penicillium/Aspergillus types Pestalotiopsis Pithomyces Polythrincium Rusts Smuts, Periconia, Myxomycetes Stachybotrys 1 10 Tetraploa Torula Background debris (1-4+) Hyphal fragments/m3 < 10 < 10 < 10 < 10 Pollen/m3 < 10 < 10 < 10 < 10 Skin cells (1-4+) < 1+ < 1+ < Sample volume (liters) TOTAL SPORES/m Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 10 of 11

49 SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Room : Room : Art Room : Room 34 Comments (see below) None None None None Lab ID-Version : Analysis Date: 11/01/ /01/ /01/ /01/2017 raw ct. spores/m3 raw ct. spores/m3 raw ct. spores/m3 raw ct. spores/m3 Alternaria Ascospores 1 40 Basidiospores Bipolaris/Drechslera group Botrytis Cercospora Chaetomium Cladosporium Curvularia 1 10 Epicoccum Fusarium Other brown 2 20 Penicillium/Aspergillus types Pestalotiopsis Pithomyces Polythrincium Rusts Smuts, Periconia, Myxomycetes Stachybotrys Tetraploa Torula Background debris (1-4+) Hyphal fragments/m3 < 10 < < 10 Pollen/m < 10 Skin cells (1-4+) < < 1+ < 1+ Sample volume (liters) TOTAL SPORES/m Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 11 of 11

50 MoldRANGE : Extended Outdoor Comparison Outdoor Location: , Outdoor sample #1 Fungi Identified Outdoor Typical Outdoor Data for: Typical Outdoor Data for: data October in New York (n =1892) The entire year in New York (n =17440) spores/m3 very low low med high very high freq % very low low med high very high freq % Alternaria Bipolaris/Drechslera group Chaetomium Cladosporium ,500 2, ,200 2, Curvularia Epicoccum Fusarium < Nigrospora Other brown Penicillium/Aspergillus types Pestalotiopsis < 1 Pithomyces Polythrincium Stachybotrys Torula Ascospores , , 2, Basidiospores 1, ,400 7,400 14,000 > ,600 9, Botrytis Cercospora Rusts Smuts, Periconia, Myxomycetes Tetraploa < < 1 TOTAL SPORES/m3 3,000 EMLab ID: , Page 1 of 3

51 MoldRANGE : Extended Outdoor Comparison Outdoor Location: , Outdoor sample #2 Fungi Identified Outdoor Typical Outdoor Data for: Typical Outdoor Data for: data October in New York (n =1892) The entire year in New York (n =17440) spores/m3 very low low med high very high freq % very low low med high very high freq % Alternaria Bipolaris/Drechslera group Chaetomium Cladosporium 8, ,500 2, ,200 2, Curvularia Epicoccum Fusarium < Nigrospora Other brown Penicillium/Aspergillus types Pestalotiopsis < 1 Pithomyces Polythrincium Stachybotrys Torula Ascospores , , 2, Basidiospores 1, ,400 7,400 14,000 > ,600 9, Botrytis Cercospora Rusts Smuts, Periconia, Myxomycetes Tetraploa < < 1 TOTAL SPORES/m3 11,000 EMLab ID: , Page 2 of 3

52 MoldRANGE : Extended Outdoor Comparison The 'Typical Outdoor Data' represents the typical outdoor spore levels for the location and time frame indicated. The last column represents the frequency of occurrence. The very low, low, med, high, and very high values represent the 10, 20, 50, 80, and 90 percentile values of the spore type when it is detected. For example, if the frequency of occurrence is 63% and the low value is 53, it would mean that the given spore type is detected 63% of the time and, when detected, 20% of the time it is present in levels above the detection limit and below 53 spores/m3. These values are updated periodically, and if enough data is not available to make a statistically meaningful assessment, it is indicated with a dash. Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. * The spores in this category are generally capable of growing on wet building materials in addition to growing outdoors. Building related growth is dependent upon the fungal type, moisture level, type of material, and other factors. Cladosporium is one of the predominant spore types worldwide and is frequently present in high numbers. Penicillium/Aspergillus species colonize both outdoor and indoor wet surfaces rapidly and are very easily dispersed. Other genera are usually present in lesser numbers. ** These fungi are generally not found growing on wet building materials. For example, the rusts and smuts are obligate plant pathogens. However, in each group there are notable exceptions. For example, agents of wood decay are members of the basidiomycetes and high counts of a single morphological type of basidiospore on an inside sample should be considered significant. n = number of samples used to calculate data. Interpretation of the data contained in this report is left to the client or the persons who conducted the field work. This report is provided for informational and comparative purposes only and should not be relied upon for any other purpose. "Typical outdoor data" are based on the results of the analysis of samples delivered to and analyzed by and assumptions regarding the origins of those samples. Sampling techniques, contaminants infecting samples, unrepresentative samples and other similar or dissimilar factors may affect these results. In addition, may not have received and tested a representative number of samples for every region or time period. hereby disclaims any liability for any and all direct, indirect, punitive, incidental, special or consequential damages arising out of the use or interpretation of the data contained in, or any actions taken or omitted in reliance upon, this report. EMLab ID: , Page 3 of 3

53 MoldSCORE : Spore Trap Report Outdoor Sample: Outdoor sample #1 Fungi Identified Outdoor sample spores/m3 Raw Spores/ < 1K 10K >K count m3 Alternaria 4 40 Cladosporium Curvularia 3 30 Other brown 1 10 Penicillium/Aspergillus types Pithomyces 5 50 Polythrincium 2 20 Ascospores Basidiospores 38 1,500 Cercospora 1 10 Rusts 3 30 Smuts, Periconia, Myxomycetes Total 3,030 Location: Main office < 1K 10K >K count m3 Alternaria 1 10 Cladosporium 1 40 Penicillium/Aspergillus types ND < 10 Pithomyces 2 20 Stachybotrys 1 10 Ascospores 1 40 Basidiospores 1 40 Rusts ND < 10 Smuts, Periconia, Myxomycetes ND < 10 Total Score Final MoldSCORE 116 EMLab ID: , Page 1 of 20

54 MoldSCORE : Spore Trap Report Location: Room 4 < 1K 10K >K count m3 Alternaria 1 10 Bipolaris/Drechslera group 1 10 Cladosporium Curvularia 1 10 Other brown 1 10 Penicillium/Aspergillus types 1 40 Pithomyces 1 10 Basidiospores Rusts ND < 10 Smuts, Periconia, Myxomycetes 1 10 Total Score Final MoldSCORE 111 Location: Room 2b < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium Epicoccum 1 10 Other brown 1 10 Penicillium/Aspergillus types 39 1,200 Pithomyces 1 10 Ascospores 1 40 Basidiospores Rusts ND < 10 Smuts, Periconia, Myxomycetes 3 30 Total 1, Score Final MoldSCORE 237 EMLab ID: , Page 2 of 20

55 MoldSCORE : Spore Trap Report Location: Cafeteria < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium Other brown 1 10 Penicillium/Aspergillus types Basidiospores Rusts 1 10 Smuts, Periconia, Myxomycetes 1 10 Total Score Final MoldSCORE 121 Location: Music Room < 1K 10K >K count m3 Alternaria 1 10 Cladosporium Epicoccum 1 10 Penicillium/Aspergillus types 2 80 Basidiospores Rusts ND < 10 Smuts, Periconia, Myxomycetes 1 10 Total Score Final MoldSCORE 105 EMLab ID: , Page 3 of 20

56 MoldSCORE : Spore Trap Report Location: Room 20 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium 2 80 Curvularia 1 10 Other brown 2 20 Penicillium/Aspergillus types Basidiospores 1 40 Botrytis 2 20 Rusts ND < 10 Smuts, Periconia, Myxomycetes 4 40 Total Score Final MoldSCORE 136 Location: Room 19 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium 1 40 Penicillium/Aspergillus types ND < 10 Pithomyces 1 10 Basidiospores 1 40 Rusts ND < 10 Smuts, Periconia, Myxomycetes 5 50 Total Score Final MoldSCORE 112 EMLab ID: , Page 4 of 20

57 MoldSCORE : Spore Trap Report Location: Room 18 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium Penicillium/Aspergillus types 1 40 Pithomyces 1 10 Basidiospores Rusts ND < 10 Smuts, Periconia, Myxomycetes ND < 10 Total Score Final MoldSCORE Location: Library < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium Penicillium/Aspergillus types 1 40 Pestalotiopsis 1 10 Pithomyces 1 10 Basidiospores 2 80 Rusts 1 10 Smuts, Periconia, Myxomycetes 4 40 Total Score Final MoldSCORE 111 EMLab ID: , Page 5 of 20

58 MoldSCORE : Spore Trap Report Location: Computer room < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium 2 80 Other brown 1 10 Penicillium/Aspergillus types ND < 10 Basidiospores ND < 10 Rusts ND < 10 Smuts, Periconia, Myxomycetes 7 70 Total Score Final MoldSCORE 116 Location: Room 13 < 1K 10K >K count m3 Alternaria 1 10 Cladosporium Other brown 1 10 Penicillium/Aspergillus types 1 40 Pestalotiopsis 1 10 Pithomyces 1 10 Basidiospores ND < 10 Rusts ND < 10 Smuts, Periconia, Myxomycetes 8 80 Tetraploa 1 10 Total Score Final MoldSCORE 125 EMLab ID: , Page 6 of 20

59 MoldSCORE : Spore Trap Report Location: Room 12 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium 1 40 Curvularia 1 10 Penicillium/Aspergillus types 1 40 Pithomyces 1 10 Basidiospores 2 80 Rusts 1 10 Smuts, Periconia, Myxomycetes 1 10 Total Score Final MoldSCORE 106 Location: Room 11 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium Other brown 2 20 Penicillium/Aspergillus types 1 40 Pithomyces 2 20 Basidiospores 1 40 Rusts ND < 10 Smuts, Periconia, Myxomycetes 2 20 Total Score Final MoldSCORE 116 EMLab ID: , Page 7 of 20

60 MoldSCORE : Spore Trap Report Location: Room 10 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium 2 80 Curvularia 1 10 Epicoccum 1 10 Other brown 2 20 Penicillium/Aspergillus types Basidiospores 1 40 Rusts ND < 10 Smuts, Periconia, Myxomycetes 5 50 Total Score Final MoldSCORE 121 Location: Room 9A < 1K 10K >K count m3 Alternaria 1 10 Cladosporium 2 80 Other brown 3 30 Penicillium/Aspergillus types ND < 10 Pestalotiopsis 1 10 Basidiospores ND < 10 Rusts 1 10 Smuts, Periconia, Myxomycetes ND < 10 Total Score Final MoldSCORE 119 EMLab ID: , Page 8 of 20

61 MoldSCORE : Spore Trap Report Location: Room 8A < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium 7 Other brown 1 10 Penicillium/Aspergillus types ND < 10 Basidiospores 1 40 Rusts ND < 10 Smuts, Periconia, Myxomycetes 1 10 Total Score 101 Final MoldSCORE Location: Nurses office < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium Penicillium/Aspergillus types 1 40 Basidiospores ND < 10 Rusts ND < 10 Smuts, Periconia, Myxomycetes 2 20 Total Score Final MoldSCORE 107 EMLab ID: , Page 9 of 20

62 MoldSCORE : Spore Trap Report Location: Room 35 < 1K 10K >K count m3 Alternaria 2 20 Cladosporium 2 80 Curvularia 1 10 Other brown 3 30 Penicillium/Aspergillus types Pestalotiopsis 1 10 Pithomyces 3 30 Basidiospores 1 40 Rusts 1 10 Smuts, Periconia, Myxomycetes Total 1, Score Final MoldSCORE 181 Location: Maker space < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium 1 40 Other brown 1 10 Penicillium/Aspergillus types ND < 10 Basidiospores ND < 10 Rusts ND < 10 Smuts, Periconia, Myxomycetes ND < 10 Total Score 102 Final MoldSCORE EMLab ID: , Page 10 of 20

63 MoldSCORE : Spore Trap Report Location: Psych office < 1K 10K >K count m3 Alternaria 1 10 Bipolaris/Drechslera group 1 10 Cladosporium Other brown 2 20 Penicillium/Aspergillus types 2 80 Pithomyces 5 50 Ascospores 1 40 Basidiospores ND < 10 Rusts 2 20 Smuts, Periconia, Myxomycetes Total Score Final MoldSCORE 157 Location: Room 7A < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium ND < 10 Curvularia 5 50 Epicoccum 2 20 Other brown 2 20 Penicillium/Aspergillus types Pithomyces 5 50 Torula 1 10 Basidiospores ND < 10 Rusts 3 30 Smuts, Periconia, Myxomycetes Total Score Final MoldSCORE 199 EMLab ID: , Page 11 of 20

64 MoldSCORE : Spore Trap Report Location: Room 8 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium 1 40 Penicillium/Aspergillus types 1 40 Pithomyces 5 50 Basidiospores 2 80 Rusts 1 10 Smuts, Periconia, Myxomycetes Total Score Final MoldSCORE 137 Location: Room 24 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium ND < 10 Epicoccum 1 10 Penicillium/Aspergillus types ND < 10 Basidiospores 1 40 Rusts ND < 10 Smuts, Periconia, Myxomycetes 3 30 Total Score 105 Final MoldSCORE 109 EMLab ID: , Page 12 of 20

65 MoldSCORE : Spore Trap Report Location: Room 25 < 1K 10K >K count m3 Alternaria 1 10 Cladosporium 1 40 Curvularia 2 20 Other brown 1 10 Penicillium/Aspergillus types 1 40 Pestalotiopsis 1 10 Pithomyces 1 10 Ascospores 1 40 Basidiospores 1 40 Rusts 2 20 Smuts, Periconia, Myxomycetes 10 Total Score Final MoldSCORE 134 Location: Gym < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium 2 80 Other brown 1 10 Penicillium/Aspergillus types 2 80 Basidiospores 1 40 Rusts 1 10 Smuts, Periconia, Myxomycetes 1 10 Total Score Final MoldSCORE 109 EMLab ID: , Page 13 of 20

66 MoldSCORE : Spore Trap Report Location: Gym sample 2 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium ND < 10 Penicillium/Aspergillus types 1 40 Pithomyces 1 10 Stachybotrys 2 20 Basidiospores 1 40 Rusts ND < 10 Smuts, Periconia, Myxomycetes 1 10 Total Score Final MoldSCORE 132 Location: Room 14 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium 1 40 Curvularia 2 20 Penicillium/Aspergillus types ND < 10 Basidiospores ND < 10 Rusts ND < 10 Smuts, Periconia, Myxomycetes 2 20 Total Score Final MoldSCORE 111 EMLab ID: , Page 14 of 20

67 MoldSCORE : Spore Trap Report Location: Room 22 < 1K 10K >K count m3 Alternaria 2 20 Cladosporium 2 80 Curvularia 1 10 Other brown 1 10 Penicillium/Aspergillus types Pithomyces 4 40 Stachybotrys 1 10 Basidiospores 1 40 Rusts ND < 10 Smuts, Periconia, Myxomycetes Total Score Final MoldSCORE 145 Location: Room 21 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium Penicillium/Aspergillus types 2 80 Basidiospores 1 40 Rusts 1 10 Smuts, Periconia, Myxomycetes ND < 10 Total Score Final MoldSCORE 108 EMLab ID: , Page 15 of 20

68 MoldSCORE : Spore Trap Report Location: Teachers lounge < 1K 10K >K count m3 Alternaria 1 10 Cladosporium 1 40 Penicillium/Aspergillus types 121 1,200 Pithomyces 1 10 Polythrincium 1 10 Basidiospores 1 40 Rusts ND < 10 Smuts, Periconia, Myxomycetes 2 20 Total 1, Score 242 Final MoldSCORE 242 Location: Room 2A < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium ND < 10 Other brown 1 10 Penicillium/Aspergillus types ND < 10 Ascospores 1 40 Basidiospores 2 80 Rusts 1 10 Smuts, Periconia, Myxomycetes ND < 10 Total Score Final MoldSCORE EMLab ID: , Page 16 of 20

69 MoldSCORE : Spore Trap Report Location: Room 5 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium Epicoccum 1 10 Penicillium/Aspergillus types Pithomyces 1 10 Basidiospores 1 40 Rusts 1 10 Smuts, Periconia, Myxomycetes 2 20 Total Score Final MoldSCORE 141 Location: Room 6 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium 1 40 Other brown 1 10 Penicillium/Aspergillus types ND < 10 Stachybotrys 1 10 Basidiospores 1 40 Rusts ND < 10 Smuts, Periconia, Myxomycetes 3 30 Total Score Final MoldSCORE 116 EMLab ID: , Page 17 of 20

70 MoldSCORE : Spore Trap Report Location: Room 9 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium Curvularia 1 10 Epicoccum 2 20 Other brown 1 10 Penicillium/Aspergillus types 2 80 Pithomyces 2 20 Basidiospores ND < 10 Rusts 3 30 Smuts, Periconia, Myxomycetes Total Score Final MoldSCORE 165 Location: Room 7 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium ND < 10 Penicillium/Aspergillus types ND < 10 Pithomyces 1 10 Basidiospores 1 40 Rusts ND < 10 Smuts, Periconia, Myxomycetes 1 10 Total Score Final MoldSCORE 105 EMLab ID: , Page 18 of 20

71 MoldSCORE : Spore Trap Report Location: Room 23 < 1K 10K >K count m3 Alternaria 1 10 Cladosporium 2 80 Curvularia 1 10 Other brown 2 20 Penicillium/Aspergillus types 1 40 Pithomyces 2 20 Ascospores 1 40 Basidiospores 2 80 Rusts 1 10 Smuts, Periconia, Myxomycetes 8 80 Total Score Final MoldSCORE 129 Location: Art Room < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium Penicillium/Aspergillus types ND < 10 Pithomyces 1 10 Basidiospores 2 80 Rusts 1 10 Smuts, Periconia, Myxomycetes 2 20 Total Score Final MoldSCORE 110 EMLab ID: , Page 19 of 20

72 MoldSCORE : Spore Trap Report Location: Room 34 < 1K 10K >K count m3 Alternaria 1 10 Cladosporium 1 40 Penicillium/Aspergillus types 1 40 Basidiospores 1 40 Rusts ND < 10 Smuts, Periconia, Myxomycetes 1 10 Total Score Final MoldSCORE * The spores in this category are generally capable of growing on wet building materials in addition to growing outdoors. Building related growth is dependent upon the fungal type, moisture level, type of material, and other factors. Cladosporium is one of the predominant spore types worldwide and is frequently present in high numbers. Penicillium/Aspergillus species colonize both outdoor and indoor wet surfaces rapidly and are very easily dispersed. Other genera are usually present in lesser numbers. ** These fungi are generally not found growing on wet building materials. For example, the rusts and smuts are obligate plant pathogens. However, in each group there are notable exceptions. For example, agents of wood decay are members of the basidiomycetes and high counts of a single morphological type of basidiospore on an inside sample should be considered significant. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Rated on a scale from to 300. A rating less than 150 is low and indicates a low probability of spores originating inside. A rating greater than 250 is high and indicates a high probability that the spores originated from inside, presumably from indoor mold growth. A rating between 150 and 250 indicates a moderate likelihood of indoor fungal growth. MoldSCORE is NOT intended for wall cavity samples. It is intended for ambient air samples in residences. Using the analysis on other samples (like wall cavity samples) will lead to misleading results. EMLab ID: , Page 20 of 20

73 MoldSCORE : Spore Trap Report Outdoor Sample: Outdoor sample #2 Fungi Identified Outdoor sample spores/m3 Raw Spores/ < 1K 10K >K count m3 Alternaria 6 60 Cladosporium 217 8,700 Curvularia 6 60 Epicoccum 2 20 Fusarium 1 10 Other brown 3 30 Penicillium/Aspergillus types Pestalotiopsis 3 30 Pithomyces 5 50 Ascospores Basidiospores 42 1,700 Rusts 1 10 Smuts, Periconia, Myxomycetes 9 90 Total 11,320 Location: Main office < 1K 10K >K count m3 Alternaria 1 10 Cladosporium 1 40 Penicillium/Aspergillus types ND < 10 Pithomyces 2 20 Stachybotrys 1 10 Ascospores 1 40 Basidiospores 1 40 Rusts ND < 10 Smuts, Periconia, Myxomycetes ND < 10 Total Score Final MoldSCORE 116 EMLab ID: , Page 1 of 20

74 MoldSCORE : Spore Trap Report Location: Room 4 < 1K 10K >K count m3 Alternaria 1 10 Bipolaris/Drechslera group 1 10 Cladosporium Curvularia 1 10 Other brown 1 10 Penicillium/Aspergillus types 1 40 Pithomyces 1 10 Basidiospores Rusts ND < 10 Smuts, Periconia, Myxomycetes 1 10 Total Score Final MoldSCORE 118 Location: Room 2b < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium Epicoccum 1 10 Other brown 1 10 Penicillium/Aspergillus types 39 1,200 Pithomyces 1 10 Ascospores 1 40 Basidiospores Rusts ND < 10 Smuts, Periconia, Myxomycetes 3 30 Total 1, Score Final MoldSCORE 249 EMLab ID: , Page 2 of 20

75 MoldSCORE : Spore Trap Report Location: Cafeteria < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium Other brown 1 10 Penicillium/Aspergillus types Basidiospores Rusts 1 10 Smuts, Periconia, Myxomycetes 1 10 Total Score Final MoldSCORE 129 Location: Music Room < 1K 10K >K count m3 Alternaria 1 10 Cladosporium Epicoccum 1 10 Penicillium/Aspergillus types 2 80 Basidiospores Rusts ND < 10 Smuts, Periconia, Myxomycetes 1 10 Total Score Final MoldSCORE 124 EMLab ID: , Page 3 of 20

76 MoldSCORE : Spore Trap Report Location: Room 20 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium 2 80 Curvularia 1 10 Other brown 2 20 Penicillium/Aspergillus types Basidiospores 1 40 Botrytis 2 20 Rusts ND < 10 Smuts, Periconia, Myxomycetes 4 40 Total Score Final MoldSCORE 142 Location: Room 19 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium 1 40 Penicillium/Aspergillus types ND < 10 Pithomyces 1 10 Basidiospores 1 40 Rusts ND < 10 Smuts, Periconia, Myxomycetes 5 50 Total Score Final MoldSCORE 113 EMLab ID: , Page 4 of 20

77 MoldSCORE : Spore Trap Report Location: Room 18 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium Penicillium/Aspergillus types 1 40 Pithomyces 1 10 Basidiospores Rusts ND < 10 Smuts, Periconia, Myxomycetes ND < 10 Total Score Final MoldSCORE 108 Location: Library < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium Penicillium/Aspergillus types 1 40 Pestalotiopsis 1 10 Pithomyces 1 10 Basidiospores 2 80 Rusts 1 10 Smuts, Periconia, Myxomycetes 4 40 Total Score Final MoldSCORE 114 EMLab ID: , Page 5 of 20

78 MoldSCORE : Spore Trap Report Location: Computer room < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium 2 80 Other brown 1 10 Penicillium/Aspergillus types ND < 10 Basidiospores ND < 10 Rusts ND < 10 Smuts, Periconia, Myxomycetes 7 70 Total Score 114 Final MoldSCORE 117 Location: Room 13 < 1K 10K >K count m3 Alternaria 1 10 Cladosporium Other brown 1 10 Penicillium/Aspergillus types 1 40 Pestalotiopsis 1 10 Pithomyces 1 10 Basidiospores ND < 10 Rusts ND < 10 Smuts, Periconia, Myxomycetes 8 80 Tetraploa 1 10 Total Score Final MoldSCORE 128 EMLab ID: , Page 6 of 20

79 MoldSCORE : Spore Trap Report Location: Room 12 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium 1 40 Curvularia 1 10 Penicillium/Aspergillus types 1 40 Pithomyces 1 10 Basidiospores 2 80 Rusts 1 10 Smuts, Periconia, Myxomycetes 1 10 Total Score Final MoldSCORE 109 Location: Room 11 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium Other brown 2 20 Penicillium/Aspergillus types 1 40 Pithomyces 2 20 Basidiospores 1 40 Rusts ND < 10 Smuts, Periconia, Myxomycetes 2 20 Total Score Final MoldSCORE 118 EMLab ID: , Page 7 of 20

80 MoldSCORE : Spore Trap Report Location: Room 10 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium 2 80 Curvularia 1 10 Epicoccum 1 10 Other brown 2 20 Penicillium/Aspergillus types Basidiospores 1 40 Rusts ND < 10 Smuts, Periconia, Myxomycetes 5 50 Total Score Final MoldSCORE 123 Location: Room 9A < 1K 10K >K count m3 Alternaria 1 10 Cladosporium 2 80 Other brown 3 30 Penicillium/Aspergillus types ND < 10 Pestalotiopsis 1 10 Basidiospores ND < 10 Rusts 1 10 Smuts, Periconia, Myxomycetes ND < 10 Total Score 112 Final MoldSCORE 119 EMLab ID: , Page 8 of 20

81 MoldSCORE : Spore Trap Report Location: Room 8A < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium 7 Other brown 1 10 Penicillium/Aspergillus types ND < 10 Basidiospores 1 40 Rusts ND < 10 Smuts, Periconia, Myxomycetes 1 10 Total Score Final MoldSCORE 106 Location: Nurses office < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium Penicillium/Aspergillus types 1 40 Basidiospores ND < 10 Rusts ND < 10 Smuts, Periconia, Myxomycetes 2 20 Total Score 105 Final MoldSCORE 105 EMLab ID: , Page 9 of 20

82 MoldSCORE : Spore Trap Report Location: Room 35 < 1K 10K >K count m3 Alternaria 2 20 Cladosporium 2 80 Curvularia 1 10 Other brown 3 30 Penicillium/Aspergillus types Pestalotiopsis 1 10 Pithomyces 3 30 Basidiospores 1 40 Rusts 1 10 Smuts, Periconia, Myxomycetes Total 1, Score Final MoldSCORE 191 Location: Maker space < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium 1 40 Other brown 1 10 Penicillium/Aspergillus types ND < 10 Basidiospores ND < 10 Rusts ND < 10 Smuts, Periconia, Myxomycetes ND < 10 Total Score Final MoldSCORE EMLab ID: , Page 10 of 20

83 MoldSCORE : Spore Trap Report Location: Psych office < 1K 10K >K count m3 Alternaria 1 10 Bipolaris/Drechslera group 1 10 Cladosporium Other brown 2 20 Penicillium/Aspergillus types 2 80 Pithomyces 5 50 Ascospores 1 40 Basidiospores ND < 10 Rusts 2 20 Smuts, Periconia, Myxomycetes Total Score Final MoldSCORE 164 Location: Room 7A < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium ND < 10 Curvularia 5 50 Epicoccum 2 20 Other brown 2 20 Penicillium/Aspergillus types Pithomyces 5 50 Torula 1 10 Basidiospores ND < 10 Rusts 3 30 Smuts, Periconia, Myxomycetes Total Score Final MoldSCORE 204 EMLab ID: , Page 11 of 20

84 MoldSCORE : Spore Trap Report Location: Room 8 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium 1 40 Penicillium/Aspergillus types 1 40 Pithomyces 5 50 Basidiospores 2 80 Rusts 1 10 Smuts, Periconia, Myxomycetes Total Score Final MoldSCORE 140 Location: Room 24 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium ND < 10 Epicoccum 1 10 Penicillium/Aspergillus types ND < 10 Basidiospores 1 40 Rusts ND < 10 Smuts, Periconia, Myxomycetes 3 30 Total Score Final MoldSCORE 110 EMLab ID: , Page 12 of 20

85 MoldSCORE : Spore Trap Report Location: Room 25 < 1K 10K >K count m3 Alternaria 1 10 Cladosporium 1 40 Curvularia 2 20 Other brown 1 10 Penicillium/Aspergillus types 1 40 Pestalotiopsis 1 10 Pithomyces 1 10 Ascospores 1 40 Basidiospores 1 40 Rusts 2 20 Smuts, Periconia, Myxomycetes 10 Total Score Final MoldSCORE 137 Location: Gym < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium 2 80 Other brown 1 10 Penicillium/Aspergillus types 2 80 Basidiospores 1 40 Rusts 1 10 Smuts, Periconia, Myxomycetes 1 10 Total Score Final MoldSCORE 112 EMLab ID: , Page 13 of 20

86 MoldSCORE : Spore Trap Report Location: Gym sample 2 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium ND < 10 Penicillium/Aspergillus types 1 40 Pithomyces 1 10 Stachybotrys 2 20 Basidiospores 1 40 Rusts ND < 10 Smuts, Periconia, Myxomycetes 1 10 Total Score Final MoldSCORE 132 Location: Room 14 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium 1 40 Curvularia 2 20 Penicillium/Aspergillus types ND < 10 Basidiospores ND < 10 Rusts ND < 10 Smuts, Periconia, Myxomycetes 2 20 Total Score 108 Final MoldSCORE 112 EMLab ID: , Page 14 of 20

87 MoldSCORE : Spore Trap Report Location: Room 22 < 1K 10K >K count m3 Alternaria 2 20 Cladosporium 2 80 Curvularia 1 10 Other brown 1 10 Penicillium/Aspergillus types Pithomyces 4 40 Stachybotrys 1 10 Basidiospores 1 40 Rusts ND < 10 Smuts, Periconia, Myxomycetes Total Score Final MoldSCORE 153 Location: Room 21 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium Penicillium/Aspergillus types 2 80 Basidiospores 1 40 Rusts 1 10 Smuts, Periconia, Myxomycetes ND < 10 Total Score 111 Final MoldSCORE 111 EMLab ID: , Page 15 of 20

88 MoldSCORE : Spore Trap Report Location: Teachers lounge < 1K 10K >K count m3 Alternaria 1 10 Cladosporium 1 40 Penicillium/Aspergillus types 121 1,200 Pithomyces 1 10 Polythrincium 1 10 Basidiospores 1 40 Rusts ND < 10 Smuts, Periconia, Myxomycetes 2 20 Total 1, Score Final MoldSCORE 250 Location: Room 2A < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium ND < 10 Other brown 1 10 Penicillium/Aspergillus types ND < 10 Ascospores 1 40 Basidiospores 2 80 Rusts 1 10 Smuts, Periconia, Myxomycetes ND < 10 Total Score Final MoldSCORE 106 EMLab ID: , Page 16 of 20

89 MoldSCORE : Spore Trap Report Location: Room 5 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium Epicoccum 1 10 Penicillium/Aspergillus types Pithomyces 1 10 Basidiospores 1 40 Rusts 1 10 Smuts, Periconia, Myxomycetes 2 20 Total Score Final MoldSCORE 147 Location: Room 6 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium 1 40 Other brown 1 10 Penicillium/Aspergillus types ND < 10 Stachybotrys 1 10 Basidiospores 1 40 Rusts ND < 10 Smuts, Periconia, Myxomycetes 3 30 Total Score Final MoldSCORE 116 EMLab ID: , Page 17 of 20

90 MoldSCORE : Spore Trap Report Location: Room 9 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium Curvularia 1 10 Epicoccum 2 20 Other brown 1 10 Penicillium/Aspergillus types 2 80 Pithomyces 2 20 Basidiospores ND < 10 Rusts 3 30 Smuts, Periconia, Myxomycetes Total Score Final MoldSCORE 173 Location: Room 7 < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium ND < 10 Penicillium/Aspergillus types ND < 10 Pithomyces 1 10 Basidiospores 1 40 Rusts ND < 10 Smuts, Periconia, Myxomycetes 1 10 Total Score Final MoldSCORE 106 EMLab ID: , Page 18 of 20

91 MoldSCORE : Spore Trap Report Location: Room 23 < 1K 10K >K count m3 Alternaria 1 10 Cladosporium 2 80 Curvularia 1 10 Other brown 2 20 Penicillium/Aspergillus types 1 40 Pithomyces 2 20 Ascospores 1 40 Basidiospores 2 80 Rusts 1 10 Smuts, Periconia, Myxomycetes 8 80 Total Score Final MoldSCORE 134 Location: Art Room < 1K 10K >K count m3 Alternaria ND < 10 Cladosporium Penicillium/Aspergillus types ND < 10 Pithomyces 1 10 Basidiospores 2 80 Rusts 1 10 Smuts, Periconia, Myxomycetes 2 20 Total Score Final MoldSCORE 107 EMLab ID: , Page 19 of 20

92 MoldSCORE : Spore Trap Report Location: Room 34 < 1K 10K >K count m3 Alternaria 1 10 Cladosporium 1 40 Penicillium/Aspergillus types 1 40 Basidiospores 1 40 Rusts ND < 10 Smuts, Periconia, Myxomycetes 1 10 Total Score Final MoldSCORE 106 * The spores in this category are generally capable of growing on wet building materials in addition to growing outdoors. Building related growth is dependent upon the fungal type, moisture level, type of material, and other factors. Cladosporium is one of the predominant spore types worldwide and is frequently present in high numbers. Penicillium/Aspergillus species colonize both outdoor and indoor wet surfaces rapidly and are very easily dispersed. Other genera are usually present in lesser numbers. ** These fungi are generally not found growing on wet building materials. For example, the rusts and smuts are obligate plant pathogens. However, in each group there are notable exceptions. For example, agents of wood decay are members of the basidiomycetes and high counts of a single morphological type of basidiospore on an inside sample should be considered significant. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Rated on a scale from to 300. A rating less than 150 is low and indicates a low probability of spores originating inside. A rating greater than 250 is high and indicates a high probability that the spores originated from inside, presumably from indoor mold growth. A rating between 150 and 250 indicates a moderate likelihood of indoor fungal growth. MoldSCORE is NOT intended for wall cavity samples. It is intended for ambient air samples in residences. Using the analysis on other samples (like wall cavity samples) will lead to misleading results. EMLab ID: , Page 20 of 20

93 Report for: Mr. Ernest Coon Regulatory Compliance 245 Albany Ave Thornwood, NY Regarding: Project: SCAR IAQ; Scarsdale UFSD- Greenacres EML ID: Approved by: Dates of Analysis: Spore trap analysis: Technical Manager Francina Thadigiri Service SOPs: Spore trap analysis (EM-MY-S-1038) AIHA-LAP, LLC accredited service, Lab ID # All samples were received in acceptable condition unless noted in the Report Comments portion in the body of the report. Due to the nature of the analyses performed, field blank correction of results is not applied. The results relate only to the items tested. ("the Company") shall have no liability to the client or the client's customer with respect to decisions or recommendations made, actions taken or courses of conduct implemented by either the client or the client's customer as a result of or based upon the Test Results. In no event shall the Company be liable to the client with respect to the Test Results except for the Company's own willful misconduct or gross negligence nor shall the Company be liable for incidental or consequential damages or lost profits or revenues to the fullest extent such liability may be disclaimed by law, even if the Company has been advised of the possibility of such damages, lost profits or lost revenues. In no event shall the Company's liability with respect to the Test Results exceed the amount paid to the Company by the client therefor. 's LabServe reporting system includes automated fail-safes to ensure that all AIHA-LAP, LLC quality requirements are met and notifications are added to reports when any quality steps remain pending. EMLab ID: , Page 1 of 5

94 Re: SCAR IAQ; Scarsdale UFSD- Greenacres SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Mechanic space nxt to PTA Date of Sampling: Date of Receipt: Date of Report: : PTA closet storage Comments (see below) None None Lab ID-Version : Analysis Date: 10/16/ /16/2017 raw ct. % read spores/m3 raw ct. % read spores/m3 Alternaria 2 20 Ascospores Basidiospores , Bipolaris/Drechslera group Cercospora Chaetomium Cladosporium , ,600 Curvularia 1 10 Epicoccum Nigrospora Penicillium/Aspergillus types , , Pithomyces Polythrincium 1 10 Rusts Smuts, Periconia, Myxomycetes Stachybotrys Ulocladium Zygomycetes Background debris (1-4+) Hyphal fragments/m Pollen/m3 < Skin cells (1-4+) Sample volume (liters) TOTAL SPORES/m3 14,000 13,000 Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 2 of 5

95 Re: SCAR IAQ; Scarsdale UFSD- Greenacres SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Custodial office Date of Sampling: Date of Receipt: Date of Report: : Outdoor sample 1 Basement ent. Comments (see below) None None Lab ID-Version : Analysis Date: 10/16/ /16/2017 raw ct. % read spores/m3 raw ct. % read spores/m3 Alternaria Ascospores Basidiospores Bipolaris/Drechslera group 1 10 Cercospora 1 10 Chaetomium Cladosporium , ,000 Curvularia Epicoccum 4 40 Nigrospora 1 10 Penicillium/Aspergillus types , ,000 Pithomyces Polythrincium 1 10 Rusts 1 10 Smuts, Periconia, Myxomycetes Stachybotrys Ulocladium Zygomycetes Background debris (1-4+) Hyphal fragments/m Pollen/m3 < Skin cells (1-4+) 2+ < 1+ Sample volume (liters) TOTAL SPORES/m3 15, ,000 Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 3 of 5

96 Re: SCAR IAQ; Scarsdale UFSD- Greenacres SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Outdoor sample 2 courtyard Date of Sampling: Date of Receipt: Date of Report: : Custodian storage room Comments (see below) None None Lab ID-Version : Analysis Date: 10/16/ /16/2017 raw ct. % read spores/m3 raw ct. % read spores/m3 Alternaria Ascospores , Basidiospores ,700 Bipolaris/Drechslera group Cercospora 2 20 Chaetomium 1 10 Cladosporium , ,200 Curvularia 2 20 Epicoccum 5 50 Nigrospora 1 10 Penicillium/Aspergillus types ,800 Pithomyces Polythrincium Rusts 2 20 Smuts, Periconia, Myxomycetes Stachybotrys 1 10 Ulocladium Zygomycetes Background debris (1-4+) Hyphal fragments/m Pollen/m3 10 < 10 Skin cells (1-4+) < Sample volume (liters) TOTAL SPORES/m3 12,000 9, Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 4 of 5

97 Re: SCAR IAQ; Scarsdale UFSD- Greenacres Date of Sampling: Date of Receipt: Date of Report: SPORE TRAP REPORT: NON-VIABLE METHODOLOGY Location: : Boiler room Comments (see below) None Lab ID-Version : Analysis Date: 10/16/2017 raw ct. % read spores/m3 Alternaria 1 10 Ascospores Basidiospores ,700 Bipolaris/Drechslera group Cercospora Chaetomium 7 70 Cladosporium ,600 Curvularia 2 20 Epicoccum Nigrospora Penicillium/Aspergillus types ,000 Pithomyces 2 20 Polythrincium Rusts Smuts, Periconia, Myxomycetes Stachybotrys Ulocladium Zygomycetes Background debris (1-4+) 2+ Hyphal fragments/m3 50 Pollen/m3 < 10 Skin cells (1-4+) 1+ Sample volume (liters) TOTAL SPORES/m3 17,000 Comments: Spore types listed without a count or data entry were not detected during the course of the analysis for the respective sample, indicating a raw count of <1 spore. The spores of Aspergillus and Penicillium (and others such as Acremonium, Paecilomyces) are small and round with very few distinguishing characteristics. They cannot be differentiated by non-viable sampling methods. Also, some species with very small spores are easily missed, and may be undercounted. Background debris indicates the amount of non-biological particulate matter present on the trace (dust in the air) and the resulting visibility for the analyst. It is rated from 1+ (low) to 4+ (high). Counts from areas with 4+ background debris should be regarded as minimal counts and may be higher than reported. It is important to account for samples volumes when evaluating dust levels. The analytical sensitivity is the spores/m^3 divided by the raw count, expressed in spores/m^3. The limit of detection is the analytical sensitivity (in spores/m^3) multiplied by the sample volume (in liters) divided by 0 liters. For more information regarding analytical sensitivity, please contact QA by calling the laboratory. A "Version" indicated by -"x" after the Lab ID# with a value greater than 1 indicates a sample with amended data. The revision number is reflected by the value of "x". Total Spores/m3 has been rounded to two significant figures to reflect analytical precision. EMLab ID: , Page 5 of 5

98 Report for: Mr. Ernest Coon Regulatory Compliance 245 Albany Ave Thornwood, NY Regarding: Project: SCAR IAQ; Scarsdale UFSD- Greenacres EML ID: Approved by: Dates of Analysis: Spore trap analysis: Technical Manager Francina Thadigiri Service SOPs: Spore trap analysis (EM-MY-S-1038) AIHA-LAP, LLC accredited service, Lab ID # All samples were received in acceptable condition unless noted in the Report Comments portion in the body of the report. Due to the nature of the analyses performed, field blank correction of results is not applied. The results relate only to the items tested. ("the Company") shall have no liability to the client or the client's customer with respect to decisions or recommendations made, actions taken or courses of conduct implemented by either the client or the client's customer as a result of or based upon the Test Results. In no event shall the Company be liable to the client with respect to the Test Results except for the Company's own willful misconduct or gross negligence nor shall the Company be liable for incidental or consequential damages or lost profits or revenues to the fullest extent such liability may be disclaimed by law, even if the Company has been advised of the possibility of such damages, lost profits or lost revenues. In no event shall the Company's liability with respect to the Test Results exceed the amount paid to the Company by the client therefor. 's LabServe reporting system includes automated fail-safes to ensure that all AIHA-LAP, LLC quality requirements are met and notifications are added to reports when any quality steps remain pending. EMLab ID: , Page 1 of 3