Environmental factors contributing to variations in CO2 flux over a barley-rice double-cropping paddy field in the Korean Peninsula.

Understanding the CO2 flux over agricultural crop fields is critical because the temporal cycle is driven by both ecological environment and anthropogenic change. We analyzed the net ecosystem exchange of CO2 measured over a barley-rice double-cropping field using the eddy covariance method for 5 years. We conducted gap-filling based on u*-threshold criteria and partitioned the net ecosystem exchange into gross primary production and respiration. The relative importance analysis of solar radiation, temperature, soil heat flux, soil water content, and vapor deficit revealed that solar radiation and temperature were the dominant contributors to net ecosystem exchange. The annual variation in the net ecosystem exchange followed a bimodal pattern driven by CO2 uptake by both barley and rice, displaying two negative peaks in late April and mid-August. The elongation stages of the crops exhibited the highest flux. Gross primary production and respiration were closely related to solar radiation and nighttime temperature, respectively. The relative importance of the other environmental variables was affected by the cultivation season and irrigation water. In the period of rice cultivation, respiration was approximately 3 µmol m-2 s-1 higher during rice drainage than during the flooded period. The accumulated net ecosystem production was estimated to be 315 gC m-2 and 349 gC m-2 for the barley and rice growing periods, respectively, and 649 gC m-2 for the annual total. These values are comparable with the results of other studies on barley-rice double-cropping fields.

Anthropogenic and Biogenic Features of Long-Term Measured CO Flux in North Downtown Houston, Texas.

Long-term urban carbon cycle studies remain rare despite the importance of carbon for energy, air quality, and climate change. To study spatial and temporal variations of energy and carbon fluxes in a subtropical urban environment, eddy covariance flux measurements were conducted north of downtown Houston, TX, using a tall radio-tower installation. The results of the first 2 yr of measurements show that both concentrations and fluxes of CO display typical seasonal and diurnal variations in urban areas. The seasonal variation of net CO flux is driven by steady anthropogenic emissions dominated by car traffic and human respiration, moderated by the local deciduous tree foliage. Weekday-weekend differences were observed in carbon fluxes, but not concentrations, while diurnal changes were dominated by rush-hour peaks from traffic and vegetation influences. Interestingly, CO and CO concentrations, but not CO flux, exhibited long-term declines, especially comparing pre- and post-Hurricane Ike periods. A directional analysis of CO fluxes revealed that the highest fluxes typically occurred from northwest directions, most likely due to emissions from small industrial sources. Car traffic as carbon source was revealed via correlations of CO with CO during the morning rush hours, and of CO flux with traffic counts during winter time. The influence of urban vegetation on net CO fluxes was identified via correlations with daytime photosynthetically active radiation due to photosynthesis, and with nighttime temperatures due to ecosystem respiration. The study site is a net source of CO throughout all seasons.

Observational insights into aerosol formation from isoprene.

Atmospheric photooxidation of isoprene is an important source of secondary organic aerosol (SOA) and there is increasing evidence that anthropogenic oxidant emissions can enhance this SOA formation. In this work, we use ambient observations of organosulfates formed from isoprene epoxydiols (IEPOX) and methacrylic acid epoxide (MAE) and a broad suite of chemical measurements to investigate the relative importance of nitrogen oxide (NO/NO2) and hydroperoxyl (HO2) SOA formation pathways from isoprene at a forested site in California. In contrast to IEPOX, the calculated production rate of MAE was observed to be independent of temperature. This is the result of the very fast thermolysis of MPAN at high temperatures that affects the distribution of the MPAN reservoir (MPAN / MPA radical) reducing the fraction that can react with OH to form MAE and subsequently SOA (F(MAE formation)). The strong temperature dependence of F(MAE formation) helps to explain our observations of similar concentrations of IEPOX-derived organosulfates (IEPOX-OS; ~1 ng m(-3)) and MAE-derived organosulfates (MAE-OS; ~1 ng m(-3)) under cooler conditions (lower isoprene concentrations) and much higher IEPOX-OS (~20 ng m(-3)) relative to MAE-OS (<0.0005 ng m(-3)) at higher temperatures (higher isoprene concentrations). A kinetic model of IEPOX and MAE loss showed that MAE forms 10-100 times more ring-opening products than IEPOX and that both are strongly dependent on aerosol water content when aerosol pH is constant. However, the higher fraction of MAE ring opening products does not compensate for the lower MAE production under warmer conditions (higher isoprene concentrations) resulting in lower formation of MAE-derived products relative to IEPOX at the surface. In regions of high NOx, high isoprene emissions and strong vertical mixing the slower MPAN thermolysis rate aloft could increase the fraction of MPAN that forms MAE resulting in a vertically varying isoprene SOA source.

Organosulfates as tracers for secondary organic aerosol (SOA) formation from 2-methyl-3-buten-2-ol (MBO) in the atmosphere.

2-Methyl-3-buten-2-ol (MBO) is an important biogenic volatile organic compound (BVOC) emitted by pine trees and a potential precursor of atmospheric secondary organic aerosol (SOA) in forested regions. In the present study, hydroxyl radical (OH)-initiated oxidation of MBO was examined in smog chambers under varied initial nitric oxide (NO) and aerosol acidity levels. Results indicate measurable SOA from MBO under low-NO conditions. Moreover, increasing aerosol acidity was found to enhance MBO SOA. Chemical characterization of laboratory-generated MBO SOA reveals that an organosulfate species (C(5)H(12)O(6)S, MW 200) formed and was substantially enhanced with elevated aerosol acidity. Ambient fine aerosol (PM(2.5)) samples collected from the BEARPEX campaign during 2007 and 2009, as well as from the BEACHON-RoMBAS campaign during 2011, were also analyzed. The MBO-derived organosulfate characterized from laboratory-generated aerosol was observed in PM(2.5) collected from these campaigns, demonstrating that it is a molecular tracer for MBO-initiated SOA in the atmosphere. Furthermore, mass concentrations of the MBO-derived organosulfate are well correlated with MBO mixing ratio, temperature, and acidity in the field campaigns. Importantly, this compound accounted for an average of 0.25% and as high as 1% of the total organic aerosol mass during BEARPEX 2009. An epoxide intermediate generated under low-NO conditions is tentatively proposed to produce MBO SOA.

Rural southeast Texas air quality measurements during the 2006 Texas Air Quality Study.

The authors conducted air quality measurements of the criteria pollutants carbon monoxide, nitrogen oxides, and ozone together with meteorological measurements at a park site southeast of College Station, TX, during the 2006 Texas Air Quality Study II (TexAQS). Ozone, a primary focus of the measurements, was above 80 ppb during 3 days and above 75 ppb during additional 8 days in summer 2006, suggestive of possible violations of the ozone National Ambient Air Quality Standard (NAAQS) in this area. In concordance with other air quality measurements during the TexAQS II, elevated ozone mixing ratios coincided with northerly flows during days after cold front passages. Ozone background during these days was as high as 80 ppb, whereas southerly air flows generally provided for an ozone background lower than 40 ppb. Back trajectory analysis shows that local ozone mixing ratios can also be strongly affected by the Houston urban pollution plume, leading to late afternoon ozone increases of as high as 50 ppb above background under favorable transport conditions. The trajectory analysis also shows that ozone background increases steadily the longer a southern air mass resides over Texas after entering from the Gulf of Mexico. In light of these and other TexAQS findings, it appears that ozone air quality is affected throughout east Texas by both long-range and regional ozone transport, and that improvements therefore will require at least a regionally oriented instead of the current locally oriented ozone precursor reduction policies.

Numerical simulation of atmospheric CO2 concentration and flux over the Korean Peninsula using WRF-VPRM model during Korus-AQ 2016 campaign.

We conducted regional scale CO2 simulations using the Weather Research and Forecasting model (WRF) coupled with the Vegetation Photosynthesis and Respiration Model (VPRM). We contrasted simulated concentrations with column, ground and aircraft observations during the Korea-United States Air Quality (KORUS-AQ) 2016 field campaign. Overall, WRF-VPRM slightly underestimates CO2 concentrations at ground and column monitoring sites, but it significantly underestimates at an inland tower measurement site, especially within the stable (nocturnal) boundary layer in nighttime. The model successfully captures the airborne vertical profiles but showed a large offset within the planetary boundary layer (PBL) in the areas surrounding Seoul and around the Taeahn point source emissions in the west coastal area of the Korean Peninsula. A case study flight intended to capture Chinese influence observed no clear signals of long-range transport of CO2, due mainly to the much larger magnitude of background CO2 concentrations. The calculated Net Ecosystem Exchange (NEE) with flux measurements at a tower site in the South Korean Peninsula has also been evaluated comparing with CO2 flux measurements at a flux tower site, resulting in the underestimation by less than a factor of 1.