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materials. To cause lung cancer, the radioactive material must enter the lungs as a gas. It then causes progressive damage to the bronchial epithelium or lining of the lungs. What is the gas and how does it originate? Table 3.2 shows the many radioactive isotopes that are produced by the decay of the common isotope of uranium (238U). Uranium miners would be exposed to all of these, but which one would they inhale into their lungs? Because radon possesses a stable electron configuration, it tends not to combine with other elements. Like most noble elements, under normal near surface conditions, it tends to exist as separate atoms in the form of a gas. In the confined space of poorly ventilated underground mines, radioactive decay in the uranium series produces sufficient concentrations of radon to significantly increase the incidence of lung cancer. The other property that makes radon‐222 so dangerous is its short half‐life (3.825 days). Within days, most of the radon inhaled by miners decays into polonium‐218 with the emission of alpha particles (4He nuclei). Subsequently, most of the radioactive218Po decays within hours into lead‐210 with the release of more alpha particles. Lung damage leading to lung cancer largely results from continued rapid release of alpha particles over long periods of exposure. Scientific studies on radon exposure have been complicated by the fact that many miners were also smokers. It turns out that smoking and radon exposure act synergistically to multiply the risk of developing lung cancer.

      Is the general public at risk of radon exposure? Uranium is ubiquitous in the rocks of Earth's crust, and so therefore is radon production. Potassium feldspar‐bearing rocks such as granites and gneisses, black shales, and phosphates contain higher uranium concentrations (>100 ppm) than average crustal rocks (<5 ppm). They therefore pose a greater threat. Radon gas occurs in air spaces and is quite soluble in water; think of the dissolved oxygen that aqueous organisms use to respire or the carbon dioxide dissolved in carbonate beverages. Groundwater circulating through uranium‐rich rocks can dissolve substantial amounts of radon gas and concentrate radium, another carcinogenic isotope. Ordinarily, this is not a problem. The gas rises and is released to the atmosphere, where it is dispersed and diluted to very low levels. But if radon gas is released into a confined space such as a home, especially one that is well insulated and not well ventilated, radon gas concentrations can reach hazardous levels. Most radon gas enters the home through cracks in the walls and foundations, either as gas or in water from which the gas is released. Most of the remainder is released when water from radon‐contaminated wells is used, again releasing radon into the home atmosphere. The problem is especially bad in winter and spring months when homes are heated, basements flooded, and ventilation poor. As warm air in the home rises, air is drawn from the soil into the home, increasing radon concentrations. The insulation that increases heat efficiency also increases radon concentrations. What can be done to reduce the risk? Making sure that basements and foundation walls are well sealed and improving ventilation can reduce radon concentrations to acceptable levels, even in homes built on soils with high concentrations of uranium. Radon test kits can be purchased from hardware stores. If indoor radon levels exceed 4 pCi/l, remediation is recommended by the installation of indoor air pumps and ventilation pipes to remove gases from beneath basement floors. Radon remediation typically costs $1500 and is highly recommended as a health measure.

      In the following sections we have chosen a few examples, among the many that exist, to illustrate the importance of radioactive isotopes and decay series in the study of Earth materials.

       Age determinations using radioactive decay series

Decay series Decay process Decay constant (λ) Half‐life Applicable dating range
14C → 14N Beta decay 1.29 × 10−4/year 5.37 Ka <60 Ka
40K → 40Ar Electron capture 4.69 × 10−10/year 1.25 Ga 25 Ka to >4.5 Ga
87Rb → 87Sr Beta decay 1.42 × 10−11/year 48.8 Ga 10 Ma to >4.5 Ga
147Sm → 143Nd Alpha decay 6.54 × 10−12/year 106 Ga 200 Ma to >4.15 Ga
232Th → 208Pb Beta and alpha decays 4.95 × 10−11/year 14.0 Ga 10 Ma to >4.5 Ga
235U → 207Pb Beta and alpha decays 9.85 × 10−10/year 704 Ma 10 Ma to >4.5 Ga
238U → 206Pb Beta and alpha decays 1.55 × 10−10/year 4.47 Ga 10 Ma to >4.5 Ga
normal upper N equals normal upper N 0 normal e Superscript minus lamda t Schematic illustration of progressive change in the proportions of radioactive parent (N) and 
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