Public exposure to significantly elevated levels of particulate matter (PM) as a result of major fires at industrial sites is a worldwide problem. Our paper describes how the United Kingdom developed its Air Quality in Major Incidents (AQinMI) service to provide fire emission plume concentration data for use by managers at the time of the incident and to allow an informed public health response. It is one of the first civilian services of its type anywhere in the world. Based on the involvement of several of the authors in the AQinMI service, we describe the service's function, detail the nature of fires covered by the service, and report for the first time on the concentration ranges of PM to which populations may be exposed in major incident fires. We also consider the human health impacts of short-term exposure to significantly elevated PM concentrations and reflect on the appropriateness of current short-term guideline values in providing public health advice. We have analysed monitoring data for airborne PM (≤ 10 μm, PM10; ≤ 2.5 μm, PM2.5 and ≤ 1.0 μm, PM1) collected by AQinMI teams using an Osiris laser light scattering monitor, the UK Environment Agency's 'indicative standard' equipment, during deployment to 23 major incident industrial fires. In this context, 'indicative' is applied to monitoring equipment that provides confirmation of the presence of particulates and indicates a measured mass concentration value. Incident-averaged concentrations ranged from 38 to 1450 μg m− 3 for PM10 and 7 to 258 μg m− 3 for PM2.5. Of concern was that, for several incidents, 15-min averaged concentrations reached > 6500 μg m− 3 for PM10 and 650 μg m− 3 for PM2.5, though such excursions tended to be of relatively short duration. In the absence of accepted very short-term (15-min to 1-h) guideline values for PM10 and PM2.5, we have analysed the relationship between the 1-h and 24-h threshold values and whether the former can be used as a predictor of longer-term exposure. Based on this analysis, for PM10, our tentative 1-h threshold value for use in deciding whether to close public buildings or to evacuate areas is 510 μg m− 3. For PM2.5, 1-h concentrations exceeding 350 μg m− 3 might indicate longer-term exposure problems. We conclude that whilst services such as AQinMI are a positive development, there is a need to consider further the accuracy of the data provided and for the development of very short-term guideline values (i.e. minutes to hours) that responders can use to determine the appropriate public health response.
Abstract Contamination of land by persistent organic pollutants has significant implications for human health and for future development potential. Bioremediation is an effective method for reducing the concentrations of such contaminants to below harmful levels, but the presence of co‐contaminants may hinder this process. Here, we present the results of a 40‐week microcosm study in which the biodegradation of 16 United States Environmental Protection Agency (USEPA) polycyclic aromatic hydrocarbons (PAHs; total: 2,166 mg kg −1 ) was followed in the presence of 3 different concentrations of cadmium (up to 620 mg kg −1 ) and lead (up to 782 mg kg −1 ) in a high organic matter soil. In the absence of metal treatment, 82% of PAHs were removed during the study period. Lead exerts a greater negative effect on total PAH removal than cadmium at low concentrations (approximately 100 mg kg −1 ) whilst cadmium exerts the greatest effect at higher concentrations (up to −27.7% reduction). Mercury, intended as the abiotic control (approximately 1,150 mg kg −1 ), exerts the greatest effect overall (−37%). Principal Component Analysis showed that PAH degradation was strongly associated with soil respiration rate, biomass content, and Ecoplate Average Well Colour Development. During the initial phase of the experiment, reduced microbial diversity was associated with increased PAH removal, consistent with literature observations for other organic contaminants, though this association was reversed after Week 12. Degradation of higher molecular weight PAHs showed the greatest sensitivity to the health of the microbial community. The effect of metal treatments on biotic parameters in microcosms without PAH amendment is also presented.
We report on the concentration ranges and combustion source-related emission profiles of organic and inorganic species released during 34 major industrial fires in the UK. These episodic events tend to be acute in nature and demand a rapid public health risk assessment to indicate the likely impact on exposed populations. The objective of this paper is to improve our understanding of the nature, composition and potential health impacts of emissions from major incident fires and so support the risk assessment process. Real world monitoring data was obtained from portable Fourier Transform Infrared (FTIR) monitoring (Gasmet DX-4030/40) carried out as part of the UK's Air Quality in Major Incidents service. The measured substances include carbon monoxide, sulphur dioxide, nitrogen dioxide, ammonia, hydrogen chloride, hydrogen bromide, hydrogen fluoride, hydrogen cyanide, formaldehyde, 1,3-butadiene, benzene, toluene, xylenes, ethyl benzene, acrolein, phosgene, arsine, phosphine and methyl isocyanate. We evaluate the reported concentrations against Acute Exposure Guideline Values (AEGLs) and Emergency Response Planning Guidelines (ERPGs), as well as against UK, EU and WHO short-term ambient guideline values. Most exceedances of AEGL or ERPG guideline values were at levels likely only to cause discomfort to exposed populations (hydrogen cyanide, hydrogen chloride, hydrogen fluoride and formaldehyde), though for several substances the exceedances could have potentially given rise to more serious health effects (acrolein, phosphine, phosgene and methyl isocyanate). In the latter cases, the observed high concentrations are likely to be due to cross-interference from other substances that absorb in the mid-range of the infrared spectrum, particularly when the ground level plume is very concentrated.
Ponds may hold significant stocks of organic carbon in their sediments and pond creation may offer a practical application for land managers to increase carbon storage. However, ponds are overlooked in global carbon budgets. Their potential significance is suggested by the abundance of ponds throughout terrestrial biomes and their high carbon burial rates, but we lack measures of sediment carbon stocks from typical ponds. We sampled sediment from lowland temperate ponds in north east England comparing carbon stocks from ponds categorised by surrounding land use, or dominant vegetation, or drying regime, along with measures of variation within ponds. Sediment carbon varied considerably between ponds. This variation was more important than any systematic variation between pond types grouped by land use, vegetation or drying, or any variation within an individual pond. Our estimates of pond sediment organic carbon give measures that are higher than from soils in widespread habitats such as temperate grassland and woodland, suggesting that ponds are significant for carbon budgets in their own right. Ponds are relatively easy to create, are ubiquitous throughout temperate biomes and can be fitted in amongst other land uses; our results show that pond creation would be a useful and practical application to boost carbon sequestration in temperate landscapes.
Abstract Many towns and cities use passive samplers (diffusion tubes) to monitor nitrogen dioxide (NO 2 ) concentration. However, literature studies have shown large horizontal and vertical concentration gradients for diffusion tubes placed over short distances, raising concerns over the representativeness of monitoring locations. This study examines variations in NO 2 concentrations with height at two roadside locations along a busy urban road in Newcastle upon Tyne (UK) over an 8-month period. NO 2 concentrations were passively monitored at building facades (approximately 7.0 m from the roadside) at heights of 0.7 m, 1.7 m and 2.7 m to replicate child breathing height in prams and buggies, adult breathing height and the Newcastle City Council sampling height (for 2017), respectively. Paired t tests indicated that NO 2 concentrations were significantly lower at 2.7 m (4.7% lower, n = 16, p = 0.001) and 1.7 m (7.1% lower, n = 14, p = 0.007) compared with those at 0.7 m. There was no statistically significant difference between NO 2 concentrations measured at 2.7 m and 1.7 m, indicating that UK local authority practice of placing diffusion tubes at higher than adult breathing height does not result in underreporting of NO 2 concentrations for regulatory purposes. The results have clear public health implications as they provide evidence that young children, in an urban setting and close to busy roadways, may be exposed to higher NO 2 concentrations compared with adults in the same location. We have shown that such differences might not be adequately reflected in the monitoring data from municipal authorities.
Small ponds comprise a substantial portion of the total area of the Earth's inland waters. They can be powerful carbon sinks or sources, potentially significant processors of organic carbon. Our understanding of their role is constrained by the absence of information regarding their CO2 fluxes (F CO2) and how these change with wet or dry phases and across distinct pond plant communities. We monitored the F CO2 from 26 neighbouring small ponds over a 2-week drying period in late summer in 2014. The mean F CO2 on day 1 (−641 ± 1490 mg m−2 day−1) represented a net intake across the site. As ponds dried they switched to becoming CO2 sources resulting in a net site emission of CO2 by day 12 (3792 ± 2755 mg m−2 day−1) although flux rates did not vary systematically between plant communities. Significant variability in the F CO2 was observed amongst adjacent ponds on individual sampling days, resulting in marked spatial heterogeneity in CO2 processing. This large degree of temporal and spatial heterogeneity across short time periods and small distances highlights the variability in the F CO2 from temporary systems, making it hard to generalize their role in carbon cycle models.
We report on the results of a 40 week study in which the biodegradation of 16 US EPA polycyclic aromatic hydrocarbons (PAHs) was followed in microcosms containing soil of high organic carbon content (11%) in the presence and absence of lead and cadmium co-contaminants. The total spiked PAH concentration was 2166mg/kg. Mercury amendment was also made to give an abiotic control. A novel kinetic model has been developed to explain the observed biphasic nature of PAH degradation. The model assumes that PAHs are distributed across soil phases of varying degrees of bioaccessibility. The results of the analysis suggest that overall percentage PAH loss is dependent on the respective rates at which the PAHs (a) are biodegraded by soil microorganisms in pore water and bioaccessible soil phases and (b) migrate from bioaccessible to non-bioaccessible soil phases. In addition, migration of PAHs to non-bioaccessible and non-Soxhlet-extractable soil phases associated with the humin pores gives rise to an apparent removal process. The presence of metal co-contaminants shows a concentration dependent inhibition of the biological degradation processes that results in a reduction in overall degradation. Lead appears to have a marginally greater inhibitory effect than cadmium.
Episodic air pollution events that occur because of wildfires, dust storms and industrial incidents can expose populations to particulate matter (PM) concentrations in the thousands of µg m-3. Such events have increased in frequency and duration over recent years, with this trend predicted to continue in the short to medium term because of climate warming. The human health cost of episodic PM events can be significant, and inflammatory responses are measurable even after only a few hours of exposure. Consequently, advice for the protection of public health should be available as quickly as possible, yet the shortest averaging period for which PM exposure guideline values (GVs) are available is 24-h. To address this problem, we have developed a novel approach, based on Receiver Operating Characteristic (ROC) statistical analysis, that derives 1-h threshold concentrations that have a probabilistic relationship with 24-h GVs. The ROC analysis was carried out on PM10 and PM2.5 monitoring data from across the US for the period 2014–2019. Validation of the model against US Air Quality Index (AQI) 24-h breakpoint concentrations for PM showed that the maximum-observed 1-h PM concentration in any rolling 24-h averaging period is an excellent predictor of exceedances of 24-h GVs.
Fine particulate matter is considered to be the most significant ambient air pollutant in terms of potential health impacts. Therefore, it is important that regulators are able to accurately assess the exposure of populations to PM10 and PM2.5 across municipal areas. We report on the practicalities of using a laser light scattering portable particulate monitor (Turnkey Instruments DustMate), in combination with a GPS, to map PM10 and PM2.5 concentrations on city-wide scales in Newcastle upon Tyne/Gateshead (UK), during a series of walking surveys. A heated inlet is necessary to remove moisture droplets from the sampled air prior to analysis by the instrument, though this also results in the loss of volatile particulate components, particularly from the PM2.5 fraction. A co-location calibration study was carried out with a reference urban background Tapered Element Oscillating Micro-Balance/Filter Dynamics Measuring System (TEOM-FDMS) system in Newcastle that is part of the UK's Automatic Urban and Rural Network (AURN) of air quality monitoring stations. For PM10, orthogonal regression of the DustMate against TEOM-FDMS data gave a slope and intercept of 1.02 ± 0.06 and -3.7 ± 1.2, respectively (R2 = 0.73), whereas for PM2.5, the respective values were 0.78 ± 0.06 and -0.63 ± 0.55 (R2 = 0.79). These parameters are comparable to literature calibration studies using this technology. There was good agreement between simultaneous samples taken using two DustMate instruments: for PM10, a slope and intercept of 1.05 ± 0.03 and 0.36 ± 0.5, respectively (R2 = 0.73), were obtained, whereas for the PM2.5, the respective values were 0.79 ± 0.01 and 0.19 ± 0.06 (R2 = 0.86). Correction factors based on the slope and intercepts obtained from the calibration exercise were applied to raw data collected from the DustMate. An annually-normalised correction procedure was then used to account for different background particulate concentrations on different sampling days. These corrected PM10 and PM2.5 concentrations and corresponding GPS coordinates were displayed on a base map using Google Fusion Tables and Google Earth Professional. Almost all areas surveyed in Newcastle/Gateshead were well below the EU Air Quality Standards for PM10 and PM2.5.
'%3e%3cpath fill='%23012169' d='M0 0v30h60V0z'/%3e%3cpath stroke='%23fff' stroke-width='6' d='m0 0 60 30m0-30L0 30'/%3e%3cpath stroke='%23C8102E' stroke-width='4' d='m0 0 60 30m0-30L0 30' clip-path='url(%23b)'/%3e%3cpath stroke='%23fff' stroke-width='10' d='M30 0v30M0 15h60'/%3e%3cpath stroke='%23C8102E' stroke-width='6' d='M30 0v30M0 15h60'/%3e%3c/g%3e%3c/svg%3e)
