Humans continue to transform the global nitrogen cycle at a record pace, reflecting an increased combustion of fossil fuels, growing demand for nitrogen in agriculture and industry, and pervasive inefficiencies in its use. Much anthropogenic nitrogen is lost to air, water, and land to cause a cascade of environmental and human health problems. Simultaneously, food production in some parts of the world is nitrogen-deficient, highlighting inequities in the distribution of nitrogencontaining fertilizers. Optimizing the need for a key human resource while minimizing its negative consequences requires an integrated interdisciplinary approach and the development of strategies to decrease nitrogen-containing waste.

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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.

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International audienceExisting descriptions of bi-directional ammonia (NH3) land-atmosphere exchange incorporate temperature and moisture controls, and are beginning to be used in regional chemical transport models. However, such models have typically applied simpler emission factors to upscale the main NH3 emission terms. While this approach has successfully simulated the main spatial patterns on local to global scales, it fails to address the environment- and climate-dependence of emissions. To handle these issues, we outline the basis for a new modelling paradigm where both NH3 emissions and deposition are calculated online according to diurnal, seasonal and spatial differences in meteorology. We show how measurements reveal a strong, but complex pattern of climatic dependence, which is increasingly being characterized using ground-based NH3 monitoring and satellite observations, while advances in process-based modelling are illustrated for agricultural and natural sources, including a global application for seabird colonies. A future architecture for NH3 emission-deposition modelling is proposed that integrates the spatio-temporal interactions, and provides the necessary foundation to assess the consequences of climate change. Based on available measurements, a first empirical estimate suggests that 5°C warming would increase emissions by 42 per cent (28-67%). Together with increased anthropogenic activity, global NH3 emissions may increase from 65 (45-85) Tg N in 2008 to reach 132 (89-179) Tg by 2100

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