The Relationship between Radon and Geology: Sources, Transport and Indoor Accumulation
Abstract
:1. Introduction
2. The Origin of Radon
2.1. Radioactive Decay
2.2. Rocks and Soil Migration Factors
2.2.1. Permeability of Soil and Rocks
2.2.2. Diffusion
2.2.3. Pressure
2.2.4. Other Factors
- Groundwater: The presence of water in the soil can act as a barrier, slowing down the migration of radon through the soil and rocks [6]. This occurs because water molecules tend to adhere to soil particles and create a film around them, which reduces the space available for gas migration [59]. However, if water is flowing through the soil or rock, it can carry dissolved radon to other areas [60]. Radon can dissolve in groundwater and be transported along with the water flow, potentially spreading the gas to other areas and increasing the risk of human exposure [61]. The concentration of radon in groundwater can vary greatly depending on the local geology and other environmental factors, and it is important to monitor the radon concentration in both groundwater and indoor air to assess the potential risk to human health [62]. Additionally, water can contribute to the accumulation of radon in indoor environments through the use of water sources such as showers and faucets, which can release radon gas into the air [63]. This was demonstrated in a recent study conducted by Ibánhez et al. (2023), who undertook an extensive survey of the Ría de Vigo catchment, a region that constitutes the most radon-prone area in the Iberian Peninsula [64]. The researchers sought to elucidate the environmental factors contributing to human exposure risk to radon during domestic water use. Their results revealed that continental waters in the area were considerably enriched in radon, with groundwater displaying levels one to two orders of magnitude higher than rivers. This was especially evident in the deeper fractured rock aquifers, where radon activity was an order of magnitude higher than in the heavily worn top regolith. Intriguingly, radon levels in the majority of the investigated waters virtually doubled during the dry season compared with the rainy season. This occurrence was related to seasonal water use, recharge cycles, and thermal convection. The authors warn that because of the high radon activity, home use of untreated groundwater results in a cumulative effective dose of radiation that is higher than the advised limit of 0.1 mSv·y−1. They advise the installation of radon remediation and mitigation measures prior to the extraction of untreated groundwater into residences, particularly during the dry season, given that over 70% of this dosage is caused by indoor water degassing and subsequent radon inhalation.
- Climatic factors: Climatic conditions, such as temperature, humidity, and precipitation, also affect the transport of radon [65]. Temperature changes can affect the pressure in the soil, leading to variations in the mobility of radon [66]. Additionally, lower temperatures typically result in higher condensation, which can restrict the diffusion of radon. Soil moisture can affect the permeability and diffusion capacity of radon [67]. Wet soil can limit the mobility of radon, acting as a barrier to gas diffusion. Excessive precipitation can saturate the soil, making it difficult for radon to diffuse and increasing the likelihood that it will be transported by groundwater [7]. On the other hand, in drier climates, the diffusion of radon can be more efficient as soil moisture is lower. The research conducted by Sundal et al. (2008) investigated the influence of various meteorological parameters on soil radon levels in permeable glacial sediments in Kinsarvik (Norway), demonstrating the importance and influence of climatic and meteorological factors [68]. The authors continuously recorded soil radon concentrations, temperature, precipitation, wind speed and direction, air pressure, and soil moisture content throughout a ten-month period. The results showed that differences in air temperature had a significant seasonal and diurnal impact on soil radon concentrations. Due to temperature variations between soil air and atmospheric air, the investigation observed air movements between regions of the ice-marginal deposit at different elevations. Notably, immediate changes in air flow direction were seen when ambient air temperatures approached the average yearly air temperature. The second most significant factor influencing soil radon concentrations was found to be air pressure. Precipitation, wind speed and direction, or soil moisture, however, had no discernible influence. The research also investigated how indoor and soil radon levels varied seasonally in a glaciofluvial deposit 40 km southwest of Kinsarvik. The seasonal fluctuation patterns in the two places were correlated, which raises the possibility that the findings may also be applicable to other regions with highly permeable building ground and variations in terrain elevation.
- Topography: The topography of the terrain also influences the transport of radon [69]. The presence of slopes, hills, and depressions can affect air circulation and soil pressure, which in turn affects the mobility of radon [70]. In areas with rugged terrain, the drainage of groundwater and air circulation may be greater, resulting in lower accumulation of radon [57]. On the other hand, depressions and low-lying areas can act as traps for radon, leading to higher concentrations of the gas. Griffiths et al. (2014) highlighted the influence of atmospheric conditions and topography on radon concentration [69]. Specifically, the radon measurements at Jungfraujoch were intermittently affected by boundary-layer air brought to the station by processes including thermally driven (anabatic) mountain winds. These observations suggest the potential for topographical features and atmospheric dynamics to significantly impact radon distribution in the environment. This highlights the importance of considering the interplay of topography and atmospheric processes when assessing radon concentrations in various geographic locations.
2.3. Accumulation of Radon in Indoor Environments
2.3.1. Radon Diffusion from the Soil
2.3.2. Ventilation and Air Pressure
2.3.3. Building Materials
2.3.4. Groundwater and Water Supply Systems
2.3.5. Radon Solubility in Water
2.3.6. Rn Accumulation
3. Health Risks Associated with Radon Exposure
- The relationship between radon exposure and lung cancer is well established [145]. When radon is inhaled, its radioactive particles can deposit in the lining of the lungs [146]. As radon and its radioactive descendants, such as 218Po and 214Po, decay, they emit radiation that can damage the DNA of lung cells and lead to the formation of tumours [147]. Epidemiological studies have shown that radon exposure is the second leading cause of lung cancer, after smoking [148]. Smokers exposed to radon have an even greater risk of developing lung cancer [140]. The study by Pershagen et al. (1994) provides a comprehensive analysis of the risk of lung cancer associated with residential radon exposure [149]. This study was conducted in Sweden and included 586 women and 774 men, aged between 35 and 74 years, who were diagnosed with lung cancer between 1980 and 1984. For comparison purposes, 1380 female controls and 1467 male controls were studied. The levels of radon measured in the residences of the study participants followed a log-normal distribution, with geometric and arithmetic means of 1.6 and 2.9 pCi/L, respectively. The results showed that the risk of lung cancer increased in relation to both estimated cumulative and time-weighted radon exposure. Compared with time-weighted average radon concentrations of up to 1.4 pCi/L, the relative risk was 1.3 (95 percent confidence interval, 1.1 to 1.6) for average radon concentrations of 3.8 to 10.8 pCi/L, and it increased to 1.8 (95 percent confidence interval, 1.1 to 2.9) at concentrations exceeding 10.8 pCi/L. An important aspect of this study was the interaction between radon exposure and smoking in relation to lung cancer. The interaction exceeded additivity and approached a multiplicative effect, suggesting that smoking may increase the risk of lung cancer associated with radon exposure. The study by Darby et al. (2005) was a collaborative analysis of individual data from 13 case-control studies on residential radon and lung cancer, encompassing nine European countries [150]. The sample included 7148 cases of lung cancer and 14,208 controls. The findings showed that the average measured radon concentration in the residences of the control group was 97 Bq·m−3, with 11% measuring over 200 Bq·m−3 and 4% measuring over 400 Bq·m−3. For the lung cancer cases, the average concentration was 104 Bq·m−3. The research found a significant correlation between radon exposure and lung cancer risk. The risk of lung cancer increased by 8.4% (with a 95% confidence interval between 3.0% and 15.8%) for each 100 Bq·m−3 increase in measured radon concentration. This corresponds to an increase of 16% (5% to 31%) per 100 Bq·m−3 increase in usual radon, i.e., after correction for the dilution caused by random uncertainties in measuring radon concentrations. The dose–response relationship appeared to be linear, with no threshold, and remained significant in analyses limited to individuals from homes with measured radon less than 200 Bq·m−3. The proportional excess risk did not significantly differ with the study, age, sex, or smoking status. In the absence of other causes of death, the absolute risks of lung cancer by age 75 at usual radon concentrations of 0, 100, and 400 Bq·m−3 would be about 0.4%, 0.5%, and 0.7%, respectively, for lifelong non-smokers, and about 25 times higher (10%, 12%, and 16%) for cigarette smokers.
- The health risks associated with radon exposure increase with cumulative exposure over time [151]. This means that even low or moderate levels of radon exposure over a long period can increase the risk of lung cancer [152]. This is especially important for individuals who spend a significant amount of time indoors, such as those who work from home or the elderly [153]. Mitigation strategies, such as improving ventilation, sealing cracks and gaps in foundations, and installing radon reduction systems, can significantly reduce radon levels in indoor environments [154]. It is also important to note that individuals who smoke are at an even greater risk of developing lung cancer from radon exposure, and therefore, should take extra precautions to reduce exposure [140]. A study by Tomasek et al. (2008) focused on examining the relationship between radon exposure and lung cancer risk in uranium miners from France and the Czech Republic [151]. They studied a group of 10,100 miners who had long-term, low-level exposure with a mean exposure time of 10 years, averaging fewer than 60 working-level months (WLM). With a total of 574 lung cancer fatalities recorded, 187% more than what would be predicted based on national statistics, the study concluded that the risk of lung cancer was much greater in this demographic. Cumulative radon exposure was closely linked to the elevated risk. According to the observed exposures, the estimated total extra relative risk per WLM was determined to be 0.027 (95% CI: 0.017–0.043). The authors discovered that for people who were exposed at the age of 30 and with 20 years since exposure, the extra relative risk per WLM was 0.042. For each ten-year rise in age at exposure and time since exposure, this risk fell by almost 50%. The study discovered no inverse exposure rate impact below 4 WL in terms of exposure rates. The outcomes were in line with the BEIR VI report’s estimations based on the concentration model when the exposure rate was less than 0.5 WL. The researchers emphasised that an important element with a substantial impact on their findings was the accuracy of exposure estimations. The most significant impact modifiers were shown to be age at exposure and time since exposure. These findings offer important insights for creating efficient methods to control and lower radon-related health hazards since they imply that both the time and duration of radon exposure are key factors in lung cancer risk in uranium miners.
- Children are considered a vulnerable group regarding radon exposure as they have a higher respiratory rate than adults and their lungs are still developing [155]. This means that in a given amount of inhaled air, children may absorb a higher amount of radon than an adult [156]. Additionally, children spend more time at home than adults, especially at younger ages when they attend school less frequently and spend most of their time at home. These factors increase the potential for exposure to radon in indoor environments, showing therefore, the importance of implementing mitigation measures in homes and schools to reduce the risk of exposure for children [157]. The study by Hill et al. (2005) provides valuable insights into the perception of radon exposure risk among rural residents receiving public health services [158]. The study based on a cross-sectional methodology and including 31 rural families showed a serious lack of knowledge about the dangers of radon exposure. It was discovered that 32% of people were exposed to high airborne radon levels (defined as 4 pCi/l). However, 39% of participants disagreed that their children’s long-term health would improve if they were exposed to less radon, 52% were unsure, and more than a third of individuals overestimated the seriousness of the health impacts that radon exposure may have. Only 21% of participants accurately identified their risk level after correcting for chance. These findings point to a worrying discrepancy between the real danger of radon exposure and how rural communities perceive that risk. This shows that there is a need for increased radon risk education and awareness, especially in rural regions where exposure can be higher. The authors came to the conclusion that low-income rural residents are unaware of the danger of radon exposure or the harmful effects of exposure. This emphasises the significance of public health initiatives meant to raise radon awareness and encourage rural residents to test themselves voluntarily. Making decisions on radon testing and mitigation requires having a thorough awareness of the danger of radon exposure. Several studies have suggested that exposure to radon may be associated with other types of cancer, such as leukaemia and stomach cancer, in addition to lung cancer [159,160,161]. However, these associations are less clear and require further research to be confirmed. On the other hand, workers in mines, underground jobs, and construction industries may be exposed to higher levels of radon compared with the general population [151]. It is now recognized that the implementation of appropriate measures to monitor and reduce the exposure to radon in the workplace is of high relevance to reducing risk and improving public health. Further research is, however, necessary to better understand the relationship between radon exposure and different types of cancer, and to inform policies and practices aimed at reducing the risk of exposure to radon in various settings. The study by Kohli et al. (2000) conducted in Sweden aimed to evaluate the relationship between exposure to ground radon and leukaemia among children, utilising existing population and disease registers [162]. The study, which examined all infants born in the county of Stergötland between 1979 and 1992, was planned as an ecological correlation study. The approach involved cross-referencing addresses in the population and property records to map each child to the centroid coordinates of the property they resided in. Radon maps were superimposed over population maps, and levels of exposure to radon were classified as high, normal, low, or unknown. The 53,146 children who participated in the research were found to have 90 malignancies, according to the study’s findings. The standardised mortality ratios (SMRs) for children born in high-, normal-, and low-risk locations for acute lymphoblastic leukaemia (ALL) were 1.43, 1.17, and 0.25, respectively. In comparison with the low-risk group, the relative risk for the high-risk and normal-risk groups was 4.64 and 5.67, respectively. The connection between ALL and continuous residency in low- or high-risk locations showed a similar pattern. Radon risk levels, however, were not linked to any other malignancies. The study concluded that children who are born and raised in regions with low ground radon risk are less likely to develop ALL than children who are born and raised in places with normal or high risk. This research adds to the growing body of information pointing to a possible link between radon exposure and the prevalence of ALL in children. Because of the limitations imposed by the study’s ecological design, more research is required to confirm and comprehend this connection. Another study by Tong et al. (2012) represents a significant contribution to our understanding of the impact of radon exposure in domestic environments on the incidence of childhood leukaemia [163]. The relationship between radon exposure and other cancers, such as leukaemia, has not always been shown, despite evidence from animal and human epidemiological research that there is an elevated risk of lung cancer in the general population. Their review sought to clarify the relationship between home radon exposure and the prevalence of childhood leukaemia by synthesising the data from ecological and case-control studies conducted in populations exposed to radon, taking into account dose estimation and evidence of radon-induced genotoxicity. The analysis of 12 ecological studies revealed a positive correlation between heightened radon levels and a higher incidence of childhood leukaemia in 11 studies, with 8 of these correlations being significant. Several case-control studies on indoor radon exposure and childhood leukaemia were reviewed alongside ecological research, and the majority of studies found a modest connection, with only a few demonstrating significance. The report also notes that the radon dose estimate is a significant source of ambiguity in radon risk assessment. One of the variables influencing risk estimations in case-control research is the techniques used to measure radon exposure in children’s homes. Through the use of genetic endpoints such as chromosomal aberration, micronuclei formation, gene mutation, and deletions and insertions, the impacts of radon-induced genetic damage were examined both in vitro and in vivo. Applying a meta-analysis, it was shown that exposure to indoor radon increased the incidence of both acute lymphoblastic leukaemia (ALL) and generalised paediatric leukaemia.
4. Risk Assessment and Mitigation
4.1. Techniques Used to Measure Radon Concentration in Rocks and Soils
4.1.1. Solid State Nuclear Track Detectors (SSNTD)
4.1.2. Ionization Chambers
4.1.3. Liquid Scintillation
4.1.4. Gamma Spectroscopy
4.1.5. Soil Permeability Measurement and Modeling
4.1.6. Uranium and Thorium Concentration Measurement Methods in Soil
4.2. Geographical and Seasonal Variations in Radon Concentration
4.2.1. Geographic Variations
4.2.2. Seasonal Variations
4.2.3. Daily Variations
4.2.4. Influence of Climate and Topography
4.3. Radon Risks Mitigation
4.3.1. Assessment and Monitoring
4.3.2. Ventilation
4.3.3. Sealing Cracks and Openings
4.3.4. Sub-Slab Radon Mitigation (SSD) System
4.3.5. Passive Soil Depressurization (PSD) Systems
4.3.6. Construction and Design of Buildings
5. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
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Lithologies | Porosity (%) |
---|---|
Arenaceous marl | 24.54–31.74 |
Basalt | 3.06 |
Gneiss | 1.21 |
Granite | 2.70 |
Limestone | 2.00–12.09 |
Marlite | 15.45–19.03 |
Sandstones | 11.95–24.94 |
Rock Type | Concentration ± Standard Deviation (Bq·kg−3) | ||
---|---|---|---|
232Th | 238U | 40K | |
Ophiolitic origin | |||
Asbestos mine waste tip material | 1.5 ± 0.1 | 1.7 ± 0.1 | 20.0 ± 0.9 |
Dunite | 1.3 ± 0.1 | 1.3 ± 0.1 | 16.9 ± 0.9 |
Gabbro | 1.8 ± 0.1 | 1.5 ± 0.6 | 71.2 ± 2.9 |
Harzburgite | 1.7 ± 0.1 | 1.2 ± 0.1 | 16.2 ± 0.8 |
Mathiatis pyrite mine tippings | 2.5 ± 1.1 | 50.5 ± 0.6 | 31.9 ± 16.8 |
Plagiogranite | 2.8 ± 0.1 | 3.0 ± 0.1 | 128.4 ± 5.0 |
Pyroxenite | 1.8 ± 0.1 | 1.1 ± 0.1 | 14.9 ± 0.7 |
Sheeted dyke complex (diabase) | 2.7 ± 0.1 | 2.7 ± 0.1 | 106.6 ± 4.2 |
Troodos lower pillow lavas (oversaturated basalt) | 2.9 ± 0.2 | 5.2 ± 0.3 | 307.2 ± 11.8 |
Troodos upper pillow lavas (olivine basalt, picrite basalt) | 3.2 ± 0.2 | 2.8 ± 0.1 | 894.2 ± 34.0 |
Wehrlite | 1.4 ± 0.1 | 0.9 ± 0.1 | 13.0 ± 0.6 |
Sedimentary origin | |||
Calcareous sandstone | 8.7 ± 0.3 | 21.7 ± 0.6 | 53.5 ± 2.4 |
Celestite | 2.4 ± 0.2 | 56.0 ± 1.5 | 17.6 ± 1.0 |
Chalk | 9.6 ± 0.3 | 5.4 ± 0.2 | 87.0 ± 3.5 |
Gypsum | 2.8 ± 0.2 | 3.8 ± 0.1 | 20.9 ± 1.1 |
Klavdhia, raised marine terrace deposits | 21.3 ± 0.7 | 90.3 ± 2.5 | 240.3 ± 9.5 |
Larnaka beach deposits | 14.9 ± 0.5 | 13.2 ± 0.5 | 127.7 ± 5.2 |
Lemesos beach deposits | 3.9 ± 0.2 | 3.1 ± 0.1 | 76.1 ± 3.0 |
Limestone | 2.1 ± 0.1 | 8.3 ± 0.3 | 20.0 ± 1.0 |
Marl (Dhali area) | 10.5 ± 0.4 | 19.1 ± 0.6 | 329.6 ± 12.8 |
Marl (Lefkosia center) | 7.1 ± 0.3 | 8.9 ± 0.3 | 187.3 ± 7.3 |
Marl (Lefkosia suburbs) | 30.8 ± 0.9 | 41.2 ± 1.2 | 433.6 ± 16.7 |
Melange | 52.8 ± 1.5 | 16.0 ± 0.5 | 392.5 ± 15.0 |
Montmorilonite (Bentonitic clay) | 40.7 ± 1.1 | 18.3 ± 0.6 | 278.9 ± 10.8 |
Paphos beach deposits | 4.8 ± 0.2 | 6.3 ± 1.2 | 147.3 ± 1.6 |
Pediaios river alluvium | 13.4 ± 0.2 | 17.6 ± 1.4 | 261.3 ± 1.5 |
Red clay soil (terra rossa) | 38.3 ± 0.5 | 21.0 ± 0.5 | 438.5 ± 10.1 |
Stratified mamonia | 20.0 ± 0.6 | 7.9 ± 0.3 | 245.3 ± 9.5 |
Geological Classes | No. of Sites (%) | Mean (Bq·m−3) |
---|---|---|
Acid rocks | 183 (5%) | 192 |
Alluvial fan | 136 (4%) | 125 |
Alluvial plain | 833 (24%) | 66 |
Alluvial plain from mountain valley | 213 (6%) | 168 |
Basic rocks | 32 (1%) | 83 |
Debris | 246 (7%) | 207 |
Dolomite rocks | 246 (7%) | 198 |
Foothill deposit | 667 (19%) | 118 |
Limestone | 333 (10%) | 137 |
Metamorphic rocks | 174 (5%) | 148 |
Moraine | 437 (12%) | 92 |
Material | No. of Samples | 226Ra (Ba·kg−1) | 222Rn Mass Exhalation Rate (mBq·kg−1·h−1) | 222Rn Emanation Factor (%) |
---|---|---|---|---|
Black sand | 6 | 13 ± 5 | 18.8 ± 6.4 | 20.4 ± 8.2 |
Cement (PPC) | 5 | 29 ± 4 | 2.3 ± 1.6 | 1.0 ± 0.7 |
Cement (SRC) | 4 | 23 ± 6 | 2.2 ± 1.9 | 1.4 ± 0.8 |
Concrete | 6 | 21 ± 5 | 8.5 ± 3.6 | 5.4 ± 1.9 |
Fired clay brick | 7 | 16 ± 5 | 6.1 ± 3.4 | 7.8 ± 3.4 |
Flyash brick | 6 | 81 ± 11 | 72.8 ± 15.3 | 11.3 ± 4.6 |
Glazed tile | 5 | 68 ± 13 | 0.8 ± 0.7 | 0.2 ± 0.2 |
Lime | 5 | 9 ± 2 | 14.6 ± 4.9 | 20.8 ± 5.2 |
Marble | 5 | 12 ± 3 | 1.1 ± 1.0 | 1.2 ± 1.1 |
Silica fume | 5 | 33 ± 8 | 12.5 ± 4.4 | 5.0 ± 1.7 |
Soil | 8 | 16 ± 7 | 23.5 ± 11.8 | 19.2 ± 6.1 |
Vitrified tile | 5 | 33 ± 5 | 0.3 ± 0.3 | 0.1 ± 0.1 |
White cement | 4 | 38 ± 7 | 12.3 ± 5.6 | 4.3 ± 1.8 |
Yellow sand | 6 | 10 ± 4 | 6.5 ± 4.3 | 8.4 ± 4.7 |
Country | Rn in Air (Bq·m−3) | Reference |
---|---|---|
Australia | 141 ± 76 | Ralph et al. (2020) |
Brazil | 227 ± 59 | Salim and Bonotto (2019) |
600 ± 787 | Ayres de Silva et al. (2018) | |
China | 80 ± 106 | Shang et al. (2015, 2008) |
530 | Chen et al. (2006) | |
400 | Chen et al. (2008) | |
169 | Fan et al. (2016) | |
India | 230 ± 66 | Rao et al. (2001) |
Iran | 321 ± 109 | Ghiassi-Nejad et al. (2002) |
220 | Fathabadi et al. (2006) | |
Pakistan | 192 | Qureshi et al. (2000) |
89 ± 28 | Mahmood and Tufail (2011) | |
Poland | 609 | Skubacz and Michalik (2002) |
261 | Bonczyk et al. (2022) | |
148 ± 111 | Skubacz et al. (2016) | |
82 ± 6 | Skubacz et al. (2019) | |
67 ± 57 | Wysocka et al. (2021) | |
Turkey | 20 | Emirhan and Ozben (2009) |
239 | Çile et al. (2010) | |
679 ± 242 | Fisne et al. (2005) | |
117 | Baldik et al. (2006) |
Country | Cave | Equilibrium Factor |
---|---|---|
Hungary | Gellért-hill System | 0.94 |
Szemlö Hill Cave | 0.50 | |
Pál Valley Cave | 0.48 | |
Therapeutic Cave | 0.51 | |
Vass Imre Cave | 0.53 | |
USA | Carlsbad Caverns | 0.44 |
Crystal Cave | 0.90 | |
Jewel Cave | 0.19 | |
Lehman Cave | 0.81 | |
Oregon Cave | 0.66 | |
Round Spring Cave | 0.98 | |
Wind Cave | 0.46 | |
Howe Caverns | 0.67 | |
Italy | Grotta Grande Vento | 0.69 |
Grotta di Quinzano | 0.55 | |
Czech Republic | Katerinska Cave | 0.75 |
Punkvevni Caves | 0.86 | |
Sloupsko-sosuvske Caves | 0.87 | |
Balcarka Cave | 1.94 | |
Japan | Akiyoshi-do Cave | 0.70 |
Taisyo-do Cave | 0.71 | |
Kagejiyo-do Cave | 0.52 | |
Slovenia | Postojna Cave | 0.56 |
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Nunes, L.J.R.; Curado, A.; Lopes, S.I. The Relationship between Radon and Geology: Sources, Transport and Indoor Accumulation. Appl. Sci. 2023, 13, 7460. https://doi.org/10.3390/app13137460
Nunes LJR, Curado A, Lopes SI. The Relationship between Radon and Geology: Sources, Transport and Indoor Accumulation. Applied Sciences. 2023; 13(13):7460. https://doi.org/10.3390/app13137460
Chicago/Turabian StyleNunes, Leonel J. R., António Curado, and Sérgio I. Lopes. 2023. "The Relationship between Radon and Geology: Sources, Transport and Indoor Accumulation" Applied Sciences 13, no. 13: 7460. https://doi.org/10.3390/app13137460
APA StyleNunes, L. J. R., Curado, A., & Lopes, S. I. (2023). The Relationship between Radon and Geology: Sources, Transport and Indoor Accumulation. Applied Sciences, 13(13), 7460. https://doi.org/10.3390/app13137460