Summary
The concentration of fungal spores, the main constituents of respirable dust in stables, is determined by rates of release from fodder and bedding and rate of clearance, principally by ventilation. This paper outlines the principles that govern the application of natural ventilation to the control of air hygiene in barns and individual boxes for horses. When release rates are low, ventilation rates over four air changes per hour are satisfactory. Ventilation was satisfactory in individual boxes but usually unsatisfactory in barns and specific recommendations are made for improvement. Preliminary observations in stables with clean, well‐managed bedding revealed only small differences between straw, wood shavings and paper. In these circumstances hay tended to be the major source of respirable spores.
An aerodynamic particle sizer (APS) that uses laser Doppler velocimetry was used to determine aerodynamic diameters of spores of fungal and thermophilic actinomycete species common in mouldy hay, aerosolized at different humidities and temperatures. Results were compared with those obtained from inertial impaction in a cascade impactor. The APS gave slightly smaller measurements than the cascade impactor. Both methods gave aerodynamic diameters generally slightly smaller than the average spore dimensions observed on cascade impactor slides with a microscope. The latter measurements were less than axial dimensions given in the literature. Brief passage of spores through air at 95% relative humidity (RH) and 38 degrees C, compared with 40% RH and 20 degrees C, caused an immediate increase in their aerodynamic diameter and the breaking of chains of spores. Cultures maintained at 75% RH and aerosolized at 98% RH similarly produced larger spore particles than those passed through dry air. These findings have implications for mould-induced asthma and allergic alveolitis since they relate to physical behaviour of airborne spores and particle deposition sites in the lung.
1. Deep litter and raised netting flooring systems in broiler houses were compared for their effects on air quality and bird health during an 8-week growing period. 2. Weekly measurements were taken of respirable dust, numbers of airborne microorganisms and concentrations of gaseous pollutants. Airborne fungi and bacteria were identified to species. 3. At the end of the experimental period, randomly sampled bird lungs were examined for the presence of viable microorganisms and for pathological changes. Bird health and performance were monitored throughout the 8 weeks. 4. Respirable dust concentrations and numbers of airborne microorganisms were significantly higher in the litter rooms. The type of floor had no effect on concentrations of gaseous ammonia. 5. Floor type had no significant effect on bird mortality but birds on litter had a slightly better gain:food ratio. However, birds on litter were observed to have a higher incidence of lung damage and more of the birds on litter had viable microorganisms present in the lungs at necropsy.
Summary
This paper describes and compares three techniques of categorisation of hay, straw and other feeds and beddings collected from stables. A hand‐held sampler was used to categorise samples according to the presence of plant material, fungal spores and dust mites. An Andersen sampler was used to categorise samples according to the thermotolerances of fungi and actinomycetes. An aerodynamic particle sizer was used to categorise samples according to respirable particle release rates. The highest burden of respirable particles was associated with the presence of thermophilic and thermotolerant actinomycetes and fungi. The portable slit sampler proved to be an accurate, quick and simple semiquantitative method of assessing the mould contamination of source materials. This latter technique requires only a microscope and the sampler, and is thus ideal for veterinary practices and small diagnostic laboratories.
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