Total column O 3 trends are used to identify ozone layer recovery and assess the Montreal Protocol's impact, but attributing their cause can be difficult because many processes affect O 3 and the process balance changes with altitude. Below 28 km, O 3 is predominantly controlled by transport because of its relatively long photochemical lifetime, but above, chemistry becomes increasingly important (Chipperfield et al., 1994). Gas phase stratospheric O 3 loss from 50 to 2 hPa (20-44 km) is predominantly controlled by the chemically reactive chlorine and nitrogen families, ClO x (Cl, Cl 2 , ClO, (ClO) 2 , OClO, and HOCl) and NO x (NO, NO 2 , NO 3 , and N 2 O 5 ) (Brasseur et al., 1999). NO x is responsible for 50%-80% of O 3 loss from ∼30 to 5 hPa but decreases in importance above as loss by ClO x increases to 30%-40% near 2 hPa; loss by HO x dominates above 2 hPa. Nitrous oxide (N 2 O), emitted at the surface, reacts with O 1 D in the tropical middle and upper stratosphere and is the primary source of NO x . NO y is the sum of reactive (NO x ) and reservoir nitrogen species (HNO 3 and ClONO 2 ); it behaves like a long-lived trace gas. Chlorofluorocarbons (CFCs), emitted at the surface and photolyzed in the stratosphere, are the primary sources of ClO x . Most of the chlorine released forms the relatively unreactive reservoir species, HCl and ClONO 2 , which then become sources for ClO x radicals involved in ozone loss cycles.Tropospheric trends in long-lived source gases cause trends in O 3 through changes in their reactive product gases. Stratospheric O 3 is expected to increase because chlorine from manmade chlorocarbons has been declining at ∼5%/decade since 2000 due to the Montreal Protocol (Engel et al., 2018), but the 3.0%/decade increase in tropospheric N 2 O (Lan et al., 2020) offsets some of that increase; stratospheric cooling reduces O 3 loss by NO x,