TY - JOUR

T1 - Seasonality of isoprene emissions and oxidation products above the remote Amazon

AU - Langford, Ben

AU - House, Emily

AU - Valach, Alex

AU - Hewitt, C N

AU - Artaxo, Paulo

AU - Barkley, Michael P.

AU - Brito, Joel

AU - Carnell, Edward J.

AU - Davison, Brian

AU - Mackenzie, A. Robert

AU - Marais, Eloise

AU - Newland, M.J.

AU - Rickard, Andrew R.

AU - Shaw, Marvin

AU - Yáñez-Serrano, A. M.

AU - Nemitz, Eiko

PY - 2022/3/31

Y1 - 2022/3/31

N2 - The Amazon rainforest is the largest source of isoprene emissions to the atmosphere globally. Under low nitric oxide (NO) conditions (i.e. at NO mixing ratios less than about 40 pptv), isoprene reacts rapidly with hydroxyl (OH) to form isoprene-derived peroxy radicals (ISOPOO), which subsequently react with the hydroperoxyl radical (HO2) to form isoprene epoxydiols (IEPOX). IEPOX compounds are efficient precursors to the formation of secondary organic aerosols (SOA). Natural isoprene emissions, therefore, have the potential to influence cloudiness, rainfall, radiation balance and climate. Here, we present the first seasonal analysis of isoprene emissions and concentrations above the Amazon based on eddy covariance flux measurements made at a remote forest location. We reveal the forest to maintain a constant emission potential of isoprene throughout the year (6.9 mg m 2 h 1). The emission potential of isoprene is calculated by normalising the measured fluxes to a set of standard conditions (303 K and 1500 mmol m 2 s 1). During the wet season a factor of two reduction in absolute emissions was observed but this is explained entirely on the basis of meteorology and leaf area index, not by a change in isoprene emissions potential. Using an innovative analysis of the isoprene fluxes, in combination with measurements of its oxidation products and detailed chemical box-modelling, we explore whether concentrations of IEPOX follow the same seasonal cycle as the isoprene precursor. Our analysis implies that during the dry season (Sep–Jan) air pollution from regional biomass burning provides a modest increase in NO concentrations (indirectly inferred from a combination of other anthropogenic tracermeasurements and box-modelling) which creates a competing oxidation pathway for ISOPOO; rather than forming IEPOX, alternative products are formed with less propensity to produce aerosol. This competition decreases IEPOX formation rates by a factor of two in the dry season compared with a scenario with no anthropogenic NO pollution, and by 30% throughout the year. The abundance of biogenic SOA precursors in the Amazon appears not to be dictated by the seasonality of natural isoprene emissions as previously thought, but is instead driven by regional anthropogenic pollution which modifies the atmospheric chemistry of isoprene.

AB - The Amazon rainforest is the largest source of isoprene emissions to the atmosphere globally. Under low nitric oxide (NO) conditions (i.e. at NO mixing ratios less than about 40 pptv), isoprene reacts rapidly with hydroxyl (OH) to form isoprene-derived peroxy radicals (ISOPOO), which subsequently react with the hydroperoxyl radical (HO2) to form isoprene epoxydiols (IEPOX). IEPOX compounds are efficient precursors to the formation of secondary organic aerosols (SOA). Natural isoprene emissions, therefore, have the potential to influence cloudiness, rainfall, radiation balance and climate. Here, we present the first seasonal analysis of isoprene emissions and concentrations above the Amazon based on eddy covariance flux measurements made at a remote forest location. We reveal the forest to maintain a constant emission potential of isoprene throughout the year (6.9 mg m 2 h 1). The emission potential of isoprene is calculated by normalising the measured fluxes to a set of standard conditions (303 K and 1500 mmol m 2 s 1). During the wet season a factor of two reduction in absolute emissions was observed but this is explained entirely on the basis of meteorology and leaf area index, not by a change in isoprene emissions potential. Using an innovative analysis of the isoprene fluxes, in combination with measurements of its oxidation products and detailed chemical box-modelling, we explore whether concentrations of IEPOX follow the same seasonal cycle as the isoprene precursor. Our analysis implies that during the dry season (Sep–Jan) air pollution from regional biomass burning provides a modest increase in NO concentrations (indirectly inferred from a combination of other anthropogenic tracermeasurements and box-modelling) which creates a competing oxidation pathway for ISOPOO; rather than forming IEPOX, alternative products are formed with less propensity to produce aerosol. This competition decreases IEPOX formation rates by a factor of two in the dry season compared with a scenario with no anthropogenic NO pollution, and by 30% throughout the year. The abundance of biogenic SOA precursors in the Amazon appears not to be dictated by the seasonality of natural isoprene emissions as previously thought, but is instead driven by regional anthropogenic pollution which modifies the atmospheric chemistry of isoprene.

U2 - 10.1039/d1ea00057h

DO - 10.1039/d1ea00057h

M3 - Journal article

VL - 2

SP - 230

EP - 240

JO - Environmental Science: Atmospheres

JF - Environmental Science: Atmospheres

IS - 2

ER -