Global nitrogen fixation contributes 413 Tg of reactive nitrogen (N r ) to terrestrial and marine ecosystems annually of which anthropogenic activities are responsible for half, 210 Tg N. The majority of the transformations of anthropogenic N r are on land (240 Tg N yr −1 ) within soils and vegetation where reduced N r contributes most of the input through the use of fertilizer nitrogen in agriculture. Leakages from the use of fertilizer N r contribute to nitrate (NO 3 − ) in drainage waters from agricultural land and emissions of trace N r compounds to the atmosphere. Emissions, mainly of ammonia (NH 3 ) from land together with combustion related emissions of nitrogen oxides (NO x ), contribute 100 Tg N yr −1 to the atmosphere, which are transported between countries and processed within the atmosphere, generating secondary pollutants, including ozone and other photochemical oxidants and aerosols, especially ammonium nitrate (NH 4 NO 3 ) and ammonium sulfate (NH 4 ) 2 SO 4 . Leaching and riverine transport of NO 3 contribute 40–70 Tg N yr −1 to coastal waters and the open ocean, which together with the 30 Tg input to oceans from atmospheric deposition combine with marine biological nitrogen fixation (140 Tg N yr −1 ) to double the ocean processing of N r . Some of the marine N r is buried in sediments, the remainder being denitrified back to the atmosphere as N 2 or N 2 O. The marine processing is of a similar magnitude to that in terrestrial soils and vegetation, but has a larger fraction of natural origin. The lifetime of N r in the atmosphere, with the exception of N 2 O, is only a few weeks, while in terrestrial ecosystems, with the exception of peatlands (where it can be 10 2 –10 3 years), the lifetime is a few decades. In the ocean, the lifetime of N r is less well known but seems to be longer than in terrestrial ecosystems and may represent an important long-term source of N 2 O that will respond very slowly to control measures on the sources of N r from which it is produced.

Abstract. Ozone holds a certain fascination in atmospheric science. It is ubiquitous in the atmosphere, central to tropospheric oxidation chemistry, yet harmful to human and ecosystem health as well as being an important greenhouse gas. It is not emitted into the atmosphere but is a byproduct of the very oxidation chemistry it largely initiates. Much effort is focused on the reduction of surface levels of ozone owing to its health and vegetation impacts, but recent efforts to achieve reductions in exposure at a country scale have proved difficult to achieve owing to increases in background ozone at the zonal hemispheric scale. There is also a growing realisation that the role of ozone as a short-lived climate pollutant could be important in integrated air quality climate change mitigation. This review examines current understanding of the processes regulating tropospheric ozone at global to local scales from both measurements and models. It takes the view that knowledge across the scales is important for dealing with air quality and climate change in a synergistic manner. The review shows that there remain a number of clear challenges for ozone such as explaining surface trends, incorporating new chemical understanding, ozone-climate coupling, and a better assessment of impacts. There is a clear and present need to treat ozone across the range of scales, a transboundary issue, but with an emphasis on the hemispheric scales. New observational opportunities are offered both by satellites and small sensors that bridge the scales.

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