Abstract

Nonmethane hydrocarbons (NMHCs) and selected halocarbons were measured in whole air samples collected over the remote Pacific Ocean during NASA's Global Tropospheric Experiment (GTE) Pacific Exploratory Mission‐Tropics B (PEM‐Tropics B) in March and early April 1999. The large‐scale spatial distributions of NMHCs and C2Cl4 reveal a much more pronounced north‐south interhemispheric gradient, with higher concentrations in the north and lower levels in the south, than for the late August to early October 1996 PEM‐Tropics A experiment. Strong continental outflow and winter‐long accumulation of pollutants led to seasonally high Northern Hemisphere trace gas levels during PEM‐Tropics B. Observations of enhanced levels of Halon 1211 (from developing Asian nations such as the PRC) and CH3Cl (from SE Asian biomass burning) support a significant southern Asian influence at altitudes above 1 km and north of 10°N. By contrast, at low altitude over the North Pacific the dominance of urban/industrial tracers, combined with low levels of Halon 1211 and CH3Cl, indicate a greater influence from developed nations such as Japan, Europe, and North America. Penetration of air exhibiting aged northern hemisphere characteristics was frequently observed at low altitudes over the equatorial central and western Pacific south to ∼5°S. The relative lack of southern hemisphere biomass burning sources and the westerly position of the South Pacific convergence zone contributed to significantly lower PEM‐Tropics B mixing ratios of the NMHCs and CH3Cl south of 10°S compared to PEM‐Tropics A. Therefore the trace gas composition of the South Pacific troposphere was considerably more representative of minimally polluted tropospheric conditions during PEM‐Tropics B.

Highlights

  • Trace gas distributionsprovide information crucial to establishingthe extent of continentalinfluence on the Nonmethanehydrocarbons(NMHCs) have diversenatural chemical environment of the remote troposphere

  • This paper focuses on results from the nonmethane comprehensivesuite of trace gas measurements.The first hydrocarbonand halocarbonanalysisof samplescollected column-detector combination

  • NMHCs for each halocarbon,the halocarbonsthat we report are are emittedfrom liquefiedpetroleumgas leakage,oil usuallypresentat mixing ratios well above their detection drilling and naturalgas fields [Blake and Rowland, 1995; limits

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Summary

Introduction

Trace gas distributionsprovide information crucial to establishingthe extent of continentalinfluence on the Nonmethanehydrocarbons(NMHCs) have diversenatural chemical environment of the remote troposphere. The reverseis true for the urban/industrial suggeststhat emissionsfrom the US were likely to tracers ethane, ethyne, propane, C2C14,and HCFC-141B, contributeto North Pacific trace gas levels, althoughtheir which displayhigher slopesversusCO for the low altitudes relativeimportanceis unknown. These low altitude air northeasterlyw, hich may allow direct mixing of emissions masseslikely represenct ombinedemissionsfrom the many from North America. Such a contribution from North developednationslocatedat mid to high northernlatitudes, American air masses is supported by the trace gas includingJapanN, orthernEurope,andNorthAmerica. Ceasedproductionof Halon 1211,buttheybumlargeamounts Averagemixing ratiosin the mid altituderange(2-8 km) of fossil fuels and use significantquantitiesof C2C14as a near the coastof CentralAmerica were significantly solventandchemicalintermediate.In addition,theseregions elevatedfor gasescharacteristicof biomassburning(e.g., tend to have a relatively low frequency of biomass ethane,ethyne,and CH3C1).

North of 10øN
Latitudinal Gradients
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