Human activity is changing air quality and climate in the US Pacific Northwest. In a first application of non-metric multidimensional scaling to a large-scale, framework dataset, we modeled lichen community response to air quality and climate gradients at 1416 forested 0.4 ha plots. Model development balanced polluted plots across elevation, forest type and precipitation ranges to isolate pollution response. Air and climate scores were fitted for remaining plots, classed by lichen bioeffects, and mapped. Projected 2040 temperatures would create climate zones with no current analogue. Worst air scores occurred in urban-industrial and agricultural valleys and represented 24% of the landscape. They were correlated with: absence of sensitive lichens, enhancement of nitrophilous lichens, mean wet deposition of ammonium >0.06 mg l-1, lichen nitrogen and sulfur concentrations >0.6% and 0.07%, and SO2 levels harmful to sensitive lichens. The model can detect changes in air quality and climate by scoring re-measurements. Lichen-based air quality and climate gradients in western Oregon and Washington are responsive to regionally increasing nitrogen availability and to temperature changes predicted by climate models.

Since the beginning of the 19th century humans have increasingly fixed atmospheric nitrogen as ammonia to be used as fertilizer. The fertilizers are necessary to create amino acids and carbohydrates in plants to feed animals and humans. The efficiency with which the fertilizers eventually reach humans is very small: 5-15%, with much of the remainder lost to the environment. The global industrial production of ammonia amounts to 117 Mton NH3-N year-1 (for 2004). By comparison, we calculate that anthropogenic emissions of NH3 to the atmosphere over the lifecycle of industrial NH3 in agriculture are 45.3 Mton NH3-N year-1, about half the industrial production. Once emitted ammonia has a central role in many environmental issues. We expect an increase in fertilizer use through increasing demands for food and biofuels as population increases. Therefore, management of ammonia or abatement is necessary. Half of industrial ammonia production is eventually lost to the global environment with significant effects.

Buffer capacity analysis of open atmospheric gas-liquid systems containing main acidic and basic atmospheric pollutants was carried out. Usually the buffer capacity is considered as a function of pH as an independent variable. In this work the buffer capacity is analysed including the dependence of pH on the composition of a system. Such an approach allows finding an important, from the viewpoint of atmospheric water acidification, relationship between the gas phase composition and the buffer capacity. It was found that buffer capacity of the open gas-liquid systems may be very high and it may cause the liquid phase pH to remain at low levels. The buffer capacity of the analysed systems is most strongly affected by the simultaneous presence of ammonia and strong acids in the gas phase. The higher concentrations of strong acid gases the lower NH₃ concentration is sufficient to achieve high buffer capacity. In the presence of strong acid gases, calcium ions affect both the buffer capacity and the liquid phase pH only at low NH₃ concentrations. High buffer capacity of open gas-liquid systems may be one of the reasons why the reduction in emissions of acidic gas pollutants has little effect on decrease in atmospheric water acidity.

Ammonia fluxes from application of anaerobically-digested slurry (ADS) and chemical fertilizer (CF) to flooded forage rice (Oryza sativa L.) in Japan were measured using a dynamic flow-through chamber method in lysimeters. The CF was applied at a rate of 300 N ha-¹ (three times) as ammoniacal-N fertilizer, and the ADS was applied to the lysimeters at total rates equivalent to 75, 100 and 150 kg N ha-¹, by broadcasting uniformly into the floodwater at three or six times (equal splits) between 17th June and 17th November, 2005. The emission fluxes for the first 2 days after application were very high from ADS, the highest values being 679 compared with a maximum of 156 mg N m-² d-¹ from CF. Most (61-93%) of the ammonia loss occurred during the first 5 days after each application of fertilizer. The total N loss as ammonia from ADS (29.6-51.7%) was much higher than from CF (12.2%). The highest fluxes were observed in August (2005) when air temperature was highest. More ammonia was lost from the ADS applied at the early stages (i.e. root taking, tiller stages) than at later stages (i.e. elongation, fruiting stages) of rice growth.

Extensive measurements were made using an Aerodyne quantum cascade laser absorption spectrometer (QCLAS) to study the diurnal and seasonal cycles of NH₃ concentrations in Manchester city centre. Measurements made at rooftop levels showed traffic to be a significant source of NH₃ concentrations in the winter. This was illustrated by a bimodal diurnal cycle of NH₃ concentrations that was synchronized with traffic, and also by a correlation with NOx, a traffic related pollutant. These patterns were not observed during the summer, suggesting other sources become more important. Measurements were also made at street level during winter and summer, close to the traffic source. This time the contribution from traffic was also observed in the summer, albeit weaker. Enhanced NH₃ concentrations were often seen in winds from the southwest that could not be related to local sources, suggesting that ambient concentrations in the city are strongly influenced by sources outside the city. It is estimated that the total NH₃ emission from the city centre is between 0.7 and 2.3 t km-² year-¹.

Ammonia (NH₃) emission from nitrogen (N) fertilizers used in agriculture decreases N uptake by the crop and negatively impacts air quality. In order to better understand the factors influencing NH₃ emission from agriculture, this research was conducted with four major soils used for potato production: Biscayne Marl Soil (BMS, pH 7.27), and Krome Gravelly Loam (KGL, pH 7.69) from Florida; and Quincy Fine Sand (QFS, pH 6.65), and Warden Silt Loam (WSL, pH 6.46) from Washington. Potassium nitrate (KNO₃), ammonium nitrate (NH₄NO₃), ammonium sulfate ((NH₄)₂SO₄) or urea ((NH)₂CO) sources were evaluated for ammonia volatilization at 75 kg N ha-¹ rate. The soil water regime was maintained at either 20 or 80% of field capacity (FC), and incubated at 11, 20 or 29°C. Results indicated that NH₃ volatilization rate at 20% FC was 2 to 3-fold greater than that at 80% FC. The cumulative volatilization loss over 28 days ranged from 0.21% of N applied as NH₄NO₃ to 25.7% as (NH₄)₂SO₄. Results of this study demonstrate that NH₃ volatilization was accelerated at the low soil water regime. Moisture quotient (Q) is defined as a ratio of NH₃ emission rate at 20% FC to that at 80% FC both at the same temperature. The peak Q values of NH₃ volatilization were up to 20.8 for the BMS soil at 20°C, 112.9 for the KGL soil at 29°C, 19.0 for the QFS soil at 20°C, and 74.1 for the WSL soil at 29°C, respectively. Thus, maintaining a suitable soil water regime is important to minimize N-loss via NH₃ volatilization and to improve N uptake efficiency and air quality.