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Dive into the research topics where Stefan Reis is active.

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Featured researches published by Stefan Reis.


Philosophical Transactions of the Royal Society B | 2013

The global nitrogen cycle in the twenty- first century

D. Fowler; Mhairi Coyle; U. Skiba; Mark A. Sutton; J. Neil Cape; Stefan Reis; Lucy J. Sheppard; Alan Jenkins; Bruna Grizzetti; James N. Galloway; Peter M. Vitousek; Allison M. Leach; A. F. Bouwman; Klaus Butterbach-Bahl; Frank Dentener; David K. Stevenson; Marcus Amann; Maren Voss

Global nitrogen fixation contributes 413 Tg of reactive nitrogen (Nr) to terrestrial and marine ecosystems annually of which anthropogenic activities are responsible for half, 210 Tg N. The majority of the transformations of anthropogenic Nr are on land (240 Tg N yr−1) within soils and vegetation where reduced Nr contributes most of the input through the use of fertilizer nitrogen in agriculture. Leakages from the use of fertilizer Nr contribute to nitrate (NO3−) in drainage waters from agricultural land and emissions of trace Nr compounds to the atmosphere. Emissions, mainly of ammonia (NH3) from land together with combustion related emissions of nitrogen oxides (NOx), 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 (NH4NO3) and ammonium sulfate (NH4)2SO4. Leaching and riverine transport of NO3 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 Nr. Some of the marine Nr is buried in sediments, the remainder being denitrified back to the atmosphere as N2 or N2O. 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 Nr in the atmosphere, with the exception of N2O, is only a few weeks, while in terrestrial ecosystems, with the exception of peatlands (where it can be 102–103 years), the lifetime is a few decades. In the ocean, the lifetime of Nr is less well known but seems to be longer than in terrestrial ecosystems and may represent an important long-term source of N2O that will respond very slowly to control measures on the sources of Nr from which it is produced.


Science of The Total Environment | 2013

Quantifying human exposure to air pollution - moving from static monitoring to spatio-temporally resolved personal exposure assessment

Susanne Steinle; Stefan Reis; Clive E. Sabel

Quantifying human exposure to air pollutants is a challenging task. Ambient concentrations of air pollutants at potentially harmful levels are ubiquitous in urban areas and subject to high spatial and temporal variability. At the same time, every individual has unique activity-patterns. Exposure results from multifaceted relationships and interactions between environmental and human systems, adding complexity to the assessment process. Traditionally, approaches to quantify human exposure have relied on pollutant concentrations from fixed air quality network sites and static population distributions. New developments in sensor technology now enable us to monitor personal exposure to air pollutants directly while people are moving through their activity spaces and varying concentration fields. The literature review on which this paper is based on reflects recent developments in the assessment of human exposure to air pollution. This includes the discussion of methodologies and concepts, and the elaboration of approaches and study designs applied in the field. We identify shortcomings of current approaches and discuss future research needs. We close by proposing a novel conceptual model for the integrated assessment of human exposure to air pollutants taking into account latest technological capabilities and contextual information.


Philosophical Transactions of the Royal Society B | 2013

Towards a climate-dependent paradigm of ammonia emission and deposition

Mark A. Sutton; Stefan Reis; Stuart N. Riddick; U. Dragosits; E. Nemitz; Mark R. Theobald; Y. Sim Tang; Christine F. Braban; Massimo Vieno; Anthony J. Dore; Sarah Wanless; Francis Daunt; D. Fowler; Trevor D. Blackall; C. Milford; Chris Flechard; Benjamin Loubet; Raia Silvia Massad; Pierre Cellier; Erwan Personne; Pierre-François Coheur; Lieven Clarisse; Martin Van Damme; Yasmine Ngadi; Cathy Clerbaux; Carsten Ambelas Skjøth; Camilla Geels; Ole Hertel; Roy Wichink Kruit; Robert W. Pinder

Existing 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.


Science of The Total Environment | 2015

Personal exposure monitoring of PM2.5 in indoor and outdoor microenvironments

Susanne Steinle; Stefan Reis; Clive E. Sabel; Sean Semple; Marsailidh Twigg; Christine F. Braban; Sarah R. Leeson; Mathew R. Heal; David Harrison; Chun Lin; Hao Wu

Adverse health effects from exposure to air pollution are a global challenge and of widespread concern. Recent high ambient concentration episodes of air pollutants in European cities highlighted the dynamic nature of human exposure and the gaps in data and knowledge about exposure patterns. In order to support health impact assessment it is essential to develop a better understanding of individual exposure pathways in peoples everyday lives by taking account of all environments in which people spend time. Here we describe the development, validation and results of an exposure method applied in a study conducted in Scotland. A low-cost particle counter based on light-scattering technology - the Dylos 1700 was used. Its performance was validated in comparison with equivalent instruments (TEOM-FDMS) at two national monitoring network sites (R(2)=0.9 at a rural background site, R(2)=0.7 at an urban background site). This validation also provided two functions to convert measured PNCs into calculated particle mass concentrations for direct comparison of concentrations with equivalent monitoring instruments and air quality limit values. This study also used contextual and time-based activity data to define six microenvironments (MEs) to assess everyday exposure of individuals to short-term PM2.5 concentrations. The Dylos was combined with a GPS receiver to track movement and exposure of individuals across the MEs. Seventeen volunteers collected 35 profiles. Profiles may have a different overall duration and structure with respect to times spent in different MEs and activities undertaken. Results indicate that due to the substantial variability across and between MEs, it is essential to measure near-complete exposure pathways to allow for a comprehensive assessment of the exposure risk a person encounters on a daily basis. Taking into account the information gained through personal exposure measurements, this work demonstrates the added value of data generated by the application of low-cost monitors.


Science | 2012

From acid rain to climate change

Stefan Reis; Peringe Grennfelt; Z. Klimont; M. Amann; Helen ApSimon; J.P. Hettelingh; M. Holland; A.-C. LeGall; Rob Maas; Maximilian Posch; Till Spranger; Mark A. Sutton; Martin L. Williams

Updated air pollution science and policies address human health, ecosystem effects, and climate change in Europe. The Convention on Long-Range Transboundary Air Pollution (CLRTAP) under the United Nations Economic Commission for Europe (UNECE) was established in 1979 to control damage to ecosystems and cultural heritage from acid rain, initially in Europe (1). Extended by eight protocols, most recently the Gothenburg Protocol (GP) signed in 1999, it has been key for developing cross-border air pollution control strategies over the UNECE region, which includes the United States and Canada. We describe how recent amendments to the GP reflect improved scientific knowledge on pollution, environmental relations, and links between regional air pollution and global climate change.


Physics and Chemistry of The Earth | 2002

Assessment of the atmospheric nitrogen and sulphur inputs into the North Sea using a Lagrangian model

O. Hertel; C.Ambelas Skjøth; Lise Marie Frohn; E. Vignati; J. Frydendall; G. de Leeuw; Uwe Schwarz; Stefan Reis

The atmospheric chemistry and deposition model has been applied for calculation of nitrogen and sulphur depositions to the entire North Sea area for the year 1999. The total atmospheric nitrogen and sulphur depositions to the North Sea area were determined to 709 kton (kt) N and 551 kt S, respectively. Since the North Sea area was calculated to be 747,988 km2, this is equivalent to an average deposition of 0.9 ton N km-2 and 0.7 ton S km-2, respectively. The depositions decrease strongly from the south end (about 2-3 kt N km-2) to the north end (about 0.2 kt N km-2) of the North Sea, due to increasing distance to the large source areas in the northern part of the European continent. The territorial waters of Belgium, the Netherlands and Germany receive about 50% higher deposition densities than the average value for the entire North Sea area. For the remaining territorial waters of the North Sea the depositions follow more or less the fraction of the area. The results furthermore show that about 60% of the total nitrogen deposition is related to emissions from combustion sources (nitrogen oxides) and about 40% from emissions related to agricultural activities (ammonia).


Archive | 2004

Emissions of Air Pollutants

Rainer Friedrich; Stefan Reis

Well founded and reliable emission data are necessary to implement strategies to investigate and control air pollution caused by the transport and chemical transformation of air pollutants. This book contains a wealth of new information that enables environmental scientists and authorities dealing with air pollution to design methods for measuring and modelling emission rates related to specific pollution sources, and thus to generate improved emission inventories and reduction strategies. Furthermore, it provides information for policy makers and environmental stakeholders concerning the main sources of emissions and the uncertainties of emission data. Scientists will obtain the know-how to carry out experiments to verify emission data, including tunnel and open motorway studies, comprehensive city experiments and tracer experiments. Readers interested in policy applications have access here to valuable information about the sources of air pollutants.


Environmental Research Letters | 2015

Impacts of European livestock production: nitrogen, sulphur, phosphorus and greenhouse gas emissions, land-use, water eutrophication and biodiversity

Adrian Leip; Gilles Billen; Josette Garnier; Bruna Grizzetti; Luis Lassaletta; Stefan Reis; David Simpson; Mark A. Sutton; Wim de Vries; Franz Weiss; Henk Westhoek

Livestock production systems currently occupy around 28% of the land surface of the European Union (equivalent to 65% of the agricultural land). In conjunction with other human activities, livestock production systems affect water, air and soil quality, global climate and biodiversity, altering the biogeochemical cycles of nitrogen, phosphorus and carbon. Here, we quantify the contribution of European livestock production to these major impacts. For each environmental effect, the contribution of livestock is expressed as shares of the emitted compounds and land used, as compared to the whole agricultural sector. The results show that the livestock sector contributes significantly to agricultural environmental impacts. This contribution is 78% for terrestrial biodiversity loss, 80% for soil acidification and air pollution (ammonia and nitrogen oxides emissions), 81% for global warming, and 73% for water pollution (both N and P). The agriculture sector itself is one of the major contributors to these environmental impacts, ranging between 12% for global warming and 59% for N water quality impact. Significant progress in mitigating these environmental impacts in Europe will only be possible through a combination of technological measures reducing livestock emissions, improved food choices and reduced food waste of European citizens.


The European Nitrogen Assessment. Sources, Effects and Policy Perspectives | 2011

Nitrogen as a threat to the European greenhouse balance

Klaus Butterbach-Bahl; E. Nemitz; Sönke Zaehle; Gilles Billen; Pascal Boeckx; Jan Willem Erisman; Josette Garnier; Robert C. Upstill-Goddard; Michael Kreuzer; O. Oenema; Stefan Reis; Martijn Schaap; David Simpson; Wim de Vries; Wilfried Winiwarter; Mark A. Sutton

Reactive nitrogen (N_r) is of fundamental importance in biological and chemical processes in the atmosphere-biosphere system, altering the Earths climate balance in many ways. These include the direct and indirect emissions of nitrous oxide (N2O), atmospheric N_r deposition and tropospheric ozone formation (O3), both of which alter the biospheric CO2 sink, N_r supply effects on CH4 emissions, and the formation of secondary atmospheric aerosols resulting from the emissions of nitrogen oxides (NOx) and ammonia (NH3). Human production and release of N_r into the environment is thus expected to have been an important driver of European greenhouse balance. Until now, no assessment has been made of how much of an effect European N_r emissions are having on net warming or cooling.


Archive | 2011

The European Nitrogen Problem in a Global Perspective

Jan Willem Erisman; Hans van Grinsven; Bruna Grizzetti; Fayçal Bouraoui; David S. Powlson; Mark A. Sutton; Albert Bleeker; Stefan Reis

Nature of the problem Reactive nitrogen has both positive and negative eff ects on ecosystems and human health. Reactive nitrogen is formed through the • use of fossil fuels releasing large amounts of nitrogen oxides into the atmosphere and through the production of ammonia by the Haber–Bosch process and using it in agriculture to increase our food, feed and fuel production. While the use of nitrogen as a fertilizer and chemical product has brought enormous benefi ts, losses of fertilizer nitrogen and combustion nitrogen to the environment lead to many side eff ects on human health, ecosystem health, biodiversity and climate.

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Mark A. Sutton

Natural Environment Research Council

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E. Nemitz

Natural Environment Research Council

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U. Skiba

University of Sheffield

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David Simpson

Norwegian Meteorological Institute

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D. Fowler

Natural Environment Research Council

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