Does Product Diversity Signal Bargains in Australian Wine?

The residuals from a set of linear regression equations built to explain the quality of a bottle of Australian wine via eight quality signals are examined to determine whether there is any relationship between their signs for individual producers and the diversity of their offerings. Product diversity is found to be a fault-ridden signal of a quality-bargain, which we define as a bottle of wine whose quality rating exceeds its regression-based expectation. Indeed, to the extent that the signal does impart useful information, the message would be that consumers are less likely to get their money's worth the greater is the diversity of the producer's offerings.wine marketing, product diversity, wine quality, predicted quality, quality-bargain, Agribusiness, Marketing,

Projecting policy – relevant metrics for high summertime ozone pollution events over the 1 Eastern United States due to climate and emission changes during the 21st century

Over the eastern United States (EUS), nitrogen oxides (NOx) emission controls have led to improved air quality over the past two decades, but concerns have been raised that climate warming may offset some of these gains. Here we analyze the effect of changing emissions and climate, in isolation and combination, on EUS summertime surface ozone (O3) over the recent past and the 21st century in an ensemble of simulations performed with the Geophysical Fluid Dynamics Laboratory CM3 chemistry-climate model. The simulated summertime EUS O3 is biased high but captures the structure of observed changes in regional O3 distributions following NOx emission reductions. We introduce a statistical bias correction, which allows derivation of policy-relevant statistics by assuming a stationary mean state bias in the model, but accurate simulation of changes at each quantile of the distribution. We contrast two different 21st century scenarios: (i) representative concentration pathway (RCP) 4.5 and (ii) simulations with well-mixed greenhouse gases (WMGG) following RCP4.5 but with emissions of air pollutants and precursors held fixed at 2005 levels (RCP4.5_WMGG). We find under RCP4.5 no exceedance of maximum daily 8 hour average ozone above 75 ppb by mid-21st century, reflecting the U.S. NOx emissions reductions projected in RCP4.5, while more than half of the EUS exceeds this level by the end of the 21st century under RCP4.5_WMGG. Further, we find a simple relationship between the changes in estimated 1 year return levels and regional NOx emission changes, implying that our results can be generalized to estimate changes in the frequency of EUS pollution events under different regional NOx emission scenarios

Effect of regional precursor emission controls on long-range ozone transport – Part 1: Short-term changes in ozone air quality

Observations and models demonstrate that ozone and its precursors can be transported between continents and across oceans. We model the influences of 10% reductions in anthropogenic nitrogen oxide (NOx) emissions from each of nine world regions on surface ozone air quality in that region and all other regions. In doing so, we quantify the relative importance of long-range transport between all source-receptor pairs, for direct short-term ozone changes. We find that for population-weighted concentrations during the three-month "ozone-season", the strongest inter-regional influences are from Europe to the Former Soviet Union, East Asia to Southeast Asia, and Europe to Africa. The largest influences per unit of NOx reduced, however, are seen for source regions in the tropics and Southern Hemisphere, which we attribute mainly to greater sensitivity to changes in NOx in the lower troposphere, and secondarily to increased vertical convection to the free troposphere in tropical regions, allowing pollutants to be transported further. Results show, for example, that NOx reductions in North America are ~20% as effective per unit NOx in reducing ozone in Europe during summer, as NOx reductions from Europe itself. Reducing anthropogenic emissions of non-methane volatile organic compounds (NMVOCs) and carbon monoxide (CO) by 10% in selected regions, can have as large an impact on long-range ozone transport as NOx reductions, depending on the source region. We find that for many source-receptor pairs, the season of greatest long-range influence does not coincide with the season when ozone is highest in the receptor region. Reducing NOx emissions in most source regions causes a larger decrease in export of ozone from the source region than in ozone production outside of the source region

Effect of regional precursor emission controls on long-range ozone transport – Part 2: Steady-state changes in ozone air quality and impacts on human mortality

Large-scale changes in ozone precursor emissions affect ozone directly in the short term, and also affect methane, which in turn causes long-term changes in ozone that affect surface ozone air quality. Here we assess the effects of changes in ozone precursor emissions on the long-term change in surface ozone via methane, as a function of the emission region, by modeling 10% reductions in anthropogenic nitrogen oxide (NOx) emissions from each of nine world regions. Reductions in NOx emissions from all world regions increase methane and long-term surface ozone. While this long-term increase is small compared to the intra-regional short-term ozone decrease, it is comparable to or larger than the short-term inter-continental ozone decrease for some source-receptor pairs. The increase in methane and long-term surface ozone per ton of NOx reduced is greatest in tropical and Southern Hemisphere regions, exceeding that from temperate Northern Hemisphere regions by roughly a factor of ten. We also assess changes in premature ozone-related human mortality associated with regional precursor reductions and long-range transport, showing that for 10% regional NOx reductions, the strongest inter-regional influence is for emissions from Europe affecting mortalities in Africa. Reductions of NOx in North America, Europe, the Former Soviet Union, and Australia are shown to reduce more mortalities outside of the source regions than within. Among world regions, NOx reductions in India cause the greatest number of avoided mortalities per ton, mainly in India itself. Finally, by increasing global methane, NOx reductions in one hemisphere tend to cause long-term increases in ozone concentration and mortalities in the opposite hemisphere. Reducing emissions of methane, and to a lesser extent carbon monoxide and non-methane volatile organic compounds, alongside NOx reductions would avoid this disbenefit

Summertime cyclones over the Great Lakes Storm Track from 1860–2100: variability, trends, and association with ozone pollution

Prior work indicates that the frequency of summertime mid-latitude cyclones tracking across the Great Lakes Storm Track (GLST, bounded by: 70° W, 90° W, 40° N, and 50° N) are strongly anticorrelated with ozone (O₃) pollution episodes over the Northeastern United States (US). We apply the MAP Climatology of Mid-latitude Storminess (MCMS) algorithm to 6-hourly sea level pressure fields from over 2500 yr of simulations with the GFDL CM3 global coupled chemistry-climate model. These simulations include (1) 875 yr with constant 1860 emissions and forcings (Pre-industrial Control), (2) five ensemble members for 1860–2005 emissions and forcings (Historical), and (3) future (2006–2100) scenarios following the Representative Concentration Pathways (RCP 4.5 and RCP 8.5) and a sensitivity simulation to isolate the role of climate warming from changes in O₃ precursor emissions (RCP 4.5*). The GFDL CM3 Historical simulations capture the mean and variability of summertime cyclones traversing the GLST within the range determined from four reanalysis datasets. Over the 21st century (2006–2100), the frequency of summertime mid-latitude cyclones in the GLST decreases under the RCP 8.5 scenario and in the RCP 4.5 ensemble mean. These trends are significant when assessed relative to the variability in the Pre-industrial Control simulation. In addition, the RCP 4.5* scenario enables us to determine the relationship between summertime GLST cyclones and high-O₃ events (> 95th percentile) in the absence of emission changes. The summertime GLST cyclone frequency explains less than 10% of the variability in high-O₃ events over the Northeastern US in the model, implying that other factors play an equally important role in determining high-O₃ events

Impact of meteorology and emissions on methane trends, 1990–2004

Over the past century, atmospheric methane (CH4) rose dramatically before leveling off in the late 1990s. The processes controlling this trend are poorly understood, limiting confidence in projections of future CH4. The MOZART-2 global tropospheric chemistry model qualitatively captures the observed CH4 trend (increasing in the early 1990s and then leveling off) with constant emissions. From 1991–1995 to 2000–2004, the CH4 lifetime versus tropospheric OH decreases by 1.6%, reflecting increases in OH and temperature. The rise in OH stems from an increase in lightning NOx as parameterized in the model. A simulation including annually varying anthropogenic and wetland CH4 emissions, as well as the changes in meteorology, best reproduces the observed CH4 distribution, trend, and seasonal cycles. Projections of future CH4 abundances should consider climate-driven changes in CH4 sources and sinks

Using synthetic tracers as a proxy for summertime PM2.5 air quality over the Northeastern United States in physical climate models

Fine particulate matter (PM2.5) is a criteria pollutant. Its sensitivity to meteorology implies its distribution will likely change with climate shifts. Limited availability of global climate models with full chemistry complicates efforts to assess rigorously the uncertainties in the PM2.5 response to a warming climate. We evaluate the potential for PM2.5 distributions in a chemistry-climate model under current-day and warmer climate conditions over the Northeastern United States to be represented by a Synthetic Aerosol tracer (SAt). The SAt implemented into the Geophysical Fluid Dynamics Laboratory chemistry-climate model (AM3) follows the protocol of a recent multimodel community effort (HTAP), with CO emissions, 25-day chemical lifetime, and wet deposition rate of sulfate. Over the Northeastern United States, the summer daily time series of SAt correlates strongly with that of PM2.5, with similar cumulative density functions under both present and future climate conditions. With a linear regression model derived from PM2.5 and SAt in the current-day simulation, we reconstruct both the current-day and future PM2.5 daily time series from the simulated SAt. This reconstruction captures the summer mean PM2.5, the incidence of days above the 24-h mean PM2.5 NAAQS, and PM2.5 responses to climate change. This reconstruction also works over other polluted Northern Hemispheric regions and in spring. Our proof-of-concept study demonstrates that simple tracers can be developed to mimic PM2.5, including its response to climate change, as an easy-to-implement and low-cost addition to physical climate models that should help air quality managers to reap the benefits of climate models that have no chemistry

Effect of sulfate aerosol on tropospheric NOx and ozone budgets: Model simulations and TOPSE evidence

The distributions of NOx and O3 are analyzed during TOPSE (Tropospheric Ozone Production about the Spring Equinox). In this study these data are compared with the calculations of a global chemical/transport model (Model for OZone And Related chemical Tracers (MOZART)). Specifically, the effect that hydrolysis of N2O5 on sulfate aerosols has on tropospheric NOx and O3 budgets is studied. The results show that without this heterogeneous reaction, the model significantly overestimates NOx concentrations at high latitudes of the Northern Hemisphere (NH) in winter and spring in comparison to the observations during TOPSE; with this reaction, modeled NOx concentrations are close to the measured values. This comparison provides evidence that the hydrolysis of N2O5 on sulfate aerosol plays an important role in controlling the tropospheric NOx and O3 budgets. The calculated reduction of NOx attributed to this reaction is 80 to 90% in winter at high latitudes over North America. Because of the reduction of NOx, O3 concentrations are also decreased. The maximum O3reduction occurs in spring although the maximum NOx reduction occurs in winter when photochemical O3 production is relatively low. The uncertainties related to uptake coefficient and aerosol loading in the model is analyzed. The analysis indicates that the changes in NOxdue to these uncertainties are much smaller than the impact of hydrolysis of N2O5 on sulfate aerosol. The effect that hydrolysis of N2O5 on global NOx and O3 budgets are also assessed by the model. The results suggest that in the Northern Hemisphere, the average NOx budget decreases 50% due to this reaction in winter and 5% in summer. The average O3 budget is reduced by 8% in winter and 6% in summer. In the Southern Hemisphere (SH), the sulfate aerosol loading is significantly smaller than in the Northern Hemisphere. As a result, sulfate aerosol has little impact on NOx and O3 budgets of the Southern Hemisphere

Sensitivity of tropospheric oxidants to biomass burning emissions: implications for radiative forcing

Biomass burning is one of the largest sources of trace gases and aerosols to the atmosphere and has profound influence on tropospheric oxidants and radiative forcing. Using a fully coupled chemistry-climate model (GFDL AM3), we find that co-emission of trace gases and aerosol from present-day biomass burning increases the global tropospheric ozone burden by 5.1% and decreases global mean OH by 6.3%. Gas and aerosol emissions combine to increase CH4 lifetime nonlinearly. Heterogeneous processes are shown to contribute partly to the observed lower ΔO3/ΔCO ratios in northern high latitudes versus tropical regions. The radiative forcing from biomass burning is shown to vary nonlinearly with biomass burning strength. At present-day emission levels, biomass burning produces a net radiative forcing of −0.19 W/m2 (−0.29 from short-lived species, mostly aerosol direct and indirect effects, +0.10 from CH4- and CH4-induced changes in O3 and stratospheric H2O) but increases emissions to over 5 times present levels would result in a positive net forcing