scholarly journals Carbon Dioxide and Methane in the China Sea Shelf Boundary Layer Observed by Cavity Ring-Down Spectroscopy

2017 ◽  
Vol 34 (10) ◽  
pp. 2233-2244 ◽  
Author(s):  
Kun-Peng Zang ◽  
Ling-Xi Zhou ◽  
Ju-Ying Wang

AbstractHigh-accuracy continuous ship-based cavity ring-down spectroscopy was used to simultaneously measure the mixing ratios of the carbon dioxide and methane in the China Sea shelf boundary layer for the first time, from 22 March to 2 April 2013. The mixing ratios of CO2 and CH4 ranged from 397.40 to 432.40 µmol mol−1 and from 1812.8 to 2068.7 nmol mol−1, respectively. Measurement data showed latitudinal distributions, with a slight fluctuation between 35.52° and 22.00°N but a sharp decline from 22.00° to 20.50°N. This distribution was not only the result of airmass transport from the Asian continent and Pacific Ocean induced by winter monsoon and trade winds but also by air–sea exchange and atmospheric chemical processes. Moreover, mixing ratios of CO2 and CH4 showed a temporal and spatial correlation that was possibly due to the effects of multisource air masses and their mixed status.

2021 ◽  
Author(s):  
Victor Lannuque ◽  
Bastien Sauvage ◽  
Brice Barret ◽  
Hannah Clark ◽  
Gilles Athier ◽  
...  

Abstract. Between December 2005 and 2013, the In-service Aircraft for a Global Observing System (IAGOS) program produced almost daily in situ measurements of CO and O3 between Europe and southern Africa. IAGOS data combined with measurements from the IASI instrument onboard the Metop-A satellite (2008–2013) are used to characterize meridional distributions and seasonality of CO and O3 in the African upper troposphere (UT). The FLEXPART particle dispersion model and the SOFT-IO model which combines the FLEXPART model with CO emission inventories are used to explore the sources and origins of the observed transects of CO and O3. We focus our analysis on two main seasons: December to March (DJFM) and June to October (JJASO). These seasons have been defined according to the position of Intertropical Convergence Zone (ITCZ), determined using in situ measurements from IAGOS. During both seasons, the UT CO meridional transects are characterized by maximum mixing ratios located 10° from the position of the ITCZ above the dry regions inside the hemisphere of the strongest Hadley cell (132 to 165 ppb at 0–5° N in DJFM and 128 to 149 ppb at 3–7° S in JJASO), and decreasing values south- and north-ward. The O3 meridional transects are characterized by mixing ratio minima of ~ 42–54 ppb at the ITCZ (10–16° S in DJFM and 5–8° N in JJASO) framed by local maxima (~ 53–71 ppb) coincident with the wind shear zones North and South of the ITCZ. O3 gradients are strongest in the hemisphere of the strongest Hadley cell. IASI UT O3 distributions in DJFM have revealed that the maxima are a part of a crescent-shaped O3 plume above the Atlantic Ocean around the Gulf of Guinea. CO emitted at the surface is transported towards the ITCZ by the trade winds and then convectively uplifted. Once in the upper troposphere, CO enriched air masses are transported away from the ITCZ by the upper branches of the Hadley cells and accumulate within the zonal wind shear zones where the maximum CO mixing ratios are found. Anthropogenic and fires both contribute, by the same order of magnitude, to the CO budget of the African upper troposphere. Local fires have the highest contribution, drive the location of the observed UT CO maxima, and are related to the following transport pathway: CO emitted at the surface is transported towards the ITCZ by the trade winds and further convectively uplifted. Then UT CO enriched air masses are transported away from the ITCZ by the upper branches of the Hadley cells and accumulate within the zonal wind shear zones where the maxima are located. Anthropogenic CO contribution is mostly from Africa during the entire year, with a low seasonal variability, and is related to similar transport circulation than fire air masses. There is also a large contribution from Asia in JJASO related to the fast convective uplift of polluted air masses in the Asian monsoon region which are further westward transported by the tropical easterly jet (TEJ) and the Asian monsoon anticyclone (AMA). O3 minima correspond to air masses that were recently uplifted from the surface where mixing ratios are low at the ITCZ. The O3 maxima correspond to old high altitude air masses uplifted from either local or long distance area of high O3 precursor emissions (Africa and South America during all the year, South Asia mainly in JJASO), and must be created during transport by photochemistry. This analysis of meridional transects contribute to a better understanding of distributions of CO and O3 in the intertropical African upper troposphere and the processes which drive these distributions. Therefore, it provides a solid basis for comparison and improvement of models and satellite products in order to get the good O3 for the good reasons.


2016 ◽  
Vol 55 (3) ◽  
pp. 507-529 ◽  
Author(s):  
B. Crawford ◽  
A. Christen ◽  
I. McKendry

AbstractObservations of carbon dioxide (CO2) mixing ratios in the urban boundary layer (UBL) are rare, even though there is potential for such measurements to be used to monitor city-scale net CO2 emissions. This work presents a unique dataset of CO2 mixing ratios observed in the UBL above Vancouver, British Columbia, Canada, by means of a tethered balloon system over a continuous 24-h summertime period. Vertical profiles of CO2 mixing ratios are found to vary according to UBL thermal structure and mechanical dynamics (development of convective and nocturnal boundary layers, vertical mixing from mechanical turbulence, horizontal advection from land–sea thermal breezes, and vertical entrainment). A box model is applied to quantify net city-scale surface emissions to the UBL volume using the measured rate of change of UBL CO2 mixing ratios and estimated CO2 advection and entrainment fluxes. The diurnal course of city-scale net emissions predicted by the model is similar to simultaneous local-scale eddy-covariance CO2 flux measurements, although there are relatively large uncertainties in hourly model calculations of horizontal advection and vertical entrainment fluxes due to inputs of regional background CO2 mixing ratios. Daily city-scale emissions totals predicted by the model (20.2 gC m−2 day−1) are 35% larger than those measured simultaneously on an urban local-scale eddy-covariance flux tower and are within 32% of a spatially scaled municipal greenhouse gas inventory. However, these methods are not expected to agree exactly because they represent different spatial source areas and include different CO2 source and sink processes.


Author(s):  
H. Pan ◽  
X.-F. Li ◽  
Y. Lu ◽  
A.-W. Liu ◽  
V.I. Perevalov ◽  
...  

2017 ◽  
Author(s):  
Brett Kuyper ◽  
Carl J. Palmer ◽  
Casper Labuschagne ◽  
Chris J. C. Reason

Abstract. Bromoform mixing ratios in marine air were measured at Cape Point Global Atmospheric Watch Station, South Africa. This represents the first ever bromoform data set recorded at this unique location. Manual daily measurements were made during a month long field campaign (austral spring 2011) using a GC-ECD with a custom built front end thermal desorption trap. The measured concentrations ranged between 2.3 ± 0.4 and 84.7 ± 10.8 ppt with a mean of 24.7 ± 3.1 ppt. Our analysis shows the concentration of bromform varies significantly according to wind direction and the trajectory of the air mass sampled. Air masses which had come into contact with multiple potential source of bromoform showed the highest average mixing ratios. The measurements reported here represent some of the highest recorded coastal bromoform concentrations globally. These high concentrations may be explained by the multiple local sources of bromoform around Cape Point.


2009 ◽  
Vol 9 (2) ◽  
pp. 6979-7032
Author(s):  
M. Saunois ◽  
C. E. Reeves ◽  
C. Mari ◽  
J. G. Murphy ◽  
D. J. Stewart ◽  
...  

Abstract. A bi-dimensional latitudinal-vertical meterological model coupled with O3-NOx-VOC chemistry is used to reproduce the distribution of ozone and precursors in the boundary layer over West Africa during the African Monsoon Multidisciplinary Analysis (AMMA) campaign as observed on board the Facility for Airborne Atmospheric Measurements (FAAM) BAe 146 Atmospheric Research Aircraft. The model reproduces the increase of ozone mixing ratios in the boundary layer observed between the forested region south of 13° N and the Sahelian area northward. Sensitivity and budget analysis reveals that the intertropical convergence zone is a moderate source of O3 rich-air in the boundary layer due to convective downdrafts. Dry deposition drives the ozone minimum over the vegetated area. The combination of high NOx emissions from soil north of 13° N and northward advection by the monsoon flux of VOC-enriched air masses contributes to the ozone maximum simulated at higher latitudes. Simulated OH exhibit a well marked latitudinal gradient with minimum concentrations over the vegetated region where the reactions with biogenic compounds predominate. The model underestimates the observed OH mixing ratios, however this model discrepancy has slight effect on ozone budget and does not alter the conclusions.


2002 ◽  
Vol 744 ◽  
Author(s):  
Susan Y. Lehman ◽  
Kris A. Bertness ◽  
Joseph T. Hodges

ABSTRACTWe are using cavity ring-down spectroscopy (CRDS) to measure concentrations of water in nitrogen and, for the first time to our knowledge, in phosphine. Water vapor concentrations have been measured in purified and unpurified phosphine, indicating a water mole fraction of (22.0 ± 1.0) x 10-6 in unpurified phosphine. After purification with an in-line, chemically-reactive purifier, the mole fraction of water in phosphine was less than 0.1 × 10-6. Mole fractions as high as (730 ± 60) × 10-6 have been measured in unpurified phosphine, suggesting that the H2O vapor concentration increases substantially with time as the gas is stored in a cylinder. The materials properties of AlInP grown by molecular beam epitaxy (MBE) with CRDS-characterized PH3 were found to be relatively insensitive to water contamination at the 22 mol/mol level.


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