Comparisons of surface flux measurement systems used in FIFE 1989

1992 ◽  
Vol 97 (D17) ◽  
pp. 18697 ◽  
Author(s):  
L. J. Fritschen ◽  
P. Qian ◽  
E. T. Kanemasu ◽  
D. Nie ◽  
E. A. Smith ◽  
...  
2012 ◽  
Vol 12 (17) ◽  
pp. 8285-8296 ◽  
Author(s):  
N. Zhang ◽  
X. Zhou ◽  
S. Bertman ◽  
D. Tang ◽  
M. Alaghmand ◽  
...  

Abstract. Systems have been developed and deployed at a North Michigan forested site to measure ambient HONO and vertical HONO flux. The modified HONO measurement technique is based on aqueous scrubbing of HONO using a coil sampler, followed by azo dye derivatization and detection using a long-path absorption photometer (LPAP). A Na2CO3-coated denuder is used to generate "zero HONO" air for background correction. The lower detection limit of the method, defined by 3 times of the standard deviation of the signal, is 1 pptv for 1-min averages, with an overall uncertainty of ±(1 + 0.05 [HONO]) pptv. The HONO flux measurement technique has been developed based on the relaxed eddy accumulation approach, deploying a 3-D sonic anemometer and two HONO measurement systems. The overall uncertainty is estimated to be within ±(8 × 10−8 + 0.15 FHONO) mol m−2 h−1, with a 20-min averaged data point per 30 min. Ambient HONO and vertical HONO flux were measured simultaneously at the PROPHET site from 17 July to 7 August 2008. The forest canopy was found to be a net HONO source, with a mean upward flux of 0.37 × 10−6 moles m−2 h−1. The HONO flux reached a maximal mean of ~0.7 × 10−6 moles m−2 h−1 around solar noon, contributing a major fraction to the HONO source strength required to sustain the observed ambient concentration of ~70 pptv. There were no significant correlations between [NOx] and daytime HONO flux and between JNO2 × [NO2] and HONO flux, suggesting that NOx was not an important precursor responsible for HONO daytime production on the forest canopy surface in this low-NOx rural environment. Evidence supports the hypothesis that photolysis of HNO3 deposited on the forest canopy surface is a major daytime HONO source.


2012 ◽  
Vol 12 (3) ◽  
pp. 7273-7304 ◽  
Author(s):  
N. Zhang ◽  
X. Zhou ◽  
S. Bertman ◽  
D. Tang ◽  
M. Alaghmand ◽  
...  

Abstract. Systems have been developed and deployed at a North Michigan forested site to measure ambient HONO and vertical HONO flux. The modified HONO measurement technique is based on aqueous scrubbing of HONO using a coil sampler, followed by azo dye derivatization and detection using an optical fiber spectrometer with a 1-m long path flow cell. A Na2CO3-coated denuder is used to generate "zero HONO" air for background correction. The lower detection limit of the method, defined by 3 times of the standard deviation of the signal, is 1 pptv for 2-min averages, with an overall uncertainty of ±(1 + 0.05 [HONO]) pptv. The HONO flux measurement technique has been developed based on the relaxed eddy accumulation approach, deploying a 3-D sonic anemometer and two HONO measurement systems. The overall uncertainty is estimated to be within ±(8 × 10−8 + 0.15 FHONO) mol m−2 h−1, with a 20-min averaged data point per 30 min. Ambient HONO and vertical HONO flux were measured simultaneously at the PROPHET site from 17 July to 7 August 2008. The forest canopy was found to be a net HONO source, with a mean upward flux of 0.37 × 10−6 moles m−2 h−1. The HONO flux reached a maximum mean of ~0.7 × 10−6 moles m−2 h−1 around solar noon, contributing a major fraction (~60%) to the HONO source strength required to sustain the observed ambient concentration of ~70 pptv. There was no significant correlation between NOx and daytime HONO flux, suggesting that NOx was not an important precursor responsible for HONO daytime production on the forest canopy surface in the low-NOx rural environment. Evidence suggests that photolysis of HNO3 deposited on the forest canopy surface is a major daytime HONO source.


1996 ◽  
Vol 82 (1-4) ◽  
pp. 119-153 ◽  
Author(s):  
Helene E. Unland ◽  
Paul R. Houser ◽  
William J. Shuttleworth ◽  
Zong-L. Yang

2004 ◽  
Author(s):  
Cale N Boriack ◽  
S.C. Capareda ◽  
R.E. Lacey ◽  
A Mutlu ◽  
S Mukhtar ◽  
...  

2009 ◽  
Vol 2 (4) ◽  
pp. 1973-2025 ◽  
Author(s):  
B. W. Blomquist ◽  
B. J. Huebert ◽  
C. W. Fairall

Abstract. Mass spectrometric measurement of DMS by atmospheric pressure ionization with an isotopically labeled standard (APIMS-ILS) is a sensitive method with sufficient bandpass for direct flux measurements by eddy correlation. Use of an isotopically labeled internal standard greatly reduces instrumental drift, improving accuracy and precision. APIMS-ILS has been used in several recent campaigns to study ocean-atmosphere gas transfer and the chemical budget of DMS in the marine boundary layer. This paper provides a comprehensive description of the method and errors associated with DMS flux measurement from ship platforms. The APIMS-ILS instrument used by most groups today has a sensitivity of 100–200 counts s−1 pptv−1, which is shown to be more than sufficient for flux measurement by eddy covariance. Mass spectral backgrounds (blanks) are determined by stripping DMS from ambient air with gold. The instrument is found to exhibit some signal loss, with a half-power frequency of ≈1 Hz, but a correction based on an empirically determined instrument response function is presented. Standard micrometeorological assumptions of steady state and horizontal uniformity are found to be appropriate for DMS flux measurement, but rapid changes in mean DMS mixing ratio serve as a warning that measured flux may not represent the true surface flux. In addition, bias in surface flux estimates arising from the flux gradient are not generally significant, but conditions of lowered inversion and high surface flux may lead to a significant difference between measured flux and true surface flux. The effects of error in motion corrections and of vertical motion within the surface layer concentration gradient are discussed and the estimated maximum error from these effects is ≤18%.


2017 ◽  
Vol 14 (12) ◽  
pp. 3027-3050 ◽  
Author(s):  
Ian D. McHugh ◽  
Jason Beringer ◽  
Shaun C. Cunningham ◽  
Patrick J. Baker ◽  
Timothy R. Cavagnaro ◽  
...  

Abstract. While the eddy covariance technique has become an important technique for estimating long-term ecosystem carbon balance, under certain conditions the measured turbulent flux of CO2 at a given height above an ecosystem does not represent the true surface flux. Profile systems have been deployed to measure periodic storage of CO2 below the measurement height, but have not been widely adopted. This is most likely due to the additional expense and complexity and possibly also the perception, given that net storage over intervals exceeding 24 h is generally negligible, that these measurements are not particularly important. In this study, we used a 3-year record of net ecosystem exchange of CO2 and simultaneous measurements of CO2 storage to ascertain the relative contributions of turbulent CO2 flux, storage, and advection (calculated as a residual quantity) to the nocturnal CO2 balance and to quantify the effect of neglecting storage. The conditions at the site are in relative terms highly favourable for eddy covariance measurements, yet we found a substantial contribution (∼ 40 %) of advection to nocturnal turbulent flux underestimation. The most likely mechanism for advection is cooling-induced drainage flows, the effects of which were observed in the storage measurements. The remaining ∼ 60 % of flux underestimation was due to storage of CO2. We also showed that substantial underestimation of carbon uptake (approximately 80 gC m−2 a−1, or 25 % of annual carbon uptake) arose when standard methods (u∗ filtering) of nocturnal flux correction were implemented in the absence of storage estimates. These biases were reduced to approximately 40–45 gC m−2 a−1 when the filter was applied over the entire diel period, but they were nonetheless large relative to quantifiable uncertainties in the data. Neglect of storage also distorted the relationships between the CO2 exchange processes (respiration and photosynthesis) and their key controls (light and temperature respectively). We conclude that the addition of storage measurements to eddy covariance sites with all but the lowest measurement heights should be a high priority for the flux measurement community.


2010 ◽  
Vol 3 (1) ◽  
pp. 1-20 ◽  
Author(s):  
B. W. Blomquist ◽  
B. J. Huebert ◽  
C. W. Fairall ◽  
I. C. Faloona

Abstract. Mass spectrometric measurement of DMS by atmospheric pressure ionization with an isotopically labeled standard (APIMS-ILS) is a sensitive method with sufficient bandpass for direct flux measurements by eddy correlation. Use of an isotopically labeled internal standard greatly reduces instrumental drift, improving accuracy and precision. APIMS-ILS has been used in several recent campaigns to study ocean-atmosphere gas transfer and the chemical budget of DMS in the marine boundary layer. This paper provides a comprehensive description of the method and errors associated with DMS flux measurement from ship platforms. The APIMS-ILS instrument used by most groups today has a sensitivity of 100–200 counts s−1 pptv−1, which is shown to be more than sufficient for flux measurement by eddy covariance. Mass spectral backgrounds (blanks) are determined by stripping DMS from ambient air with gold. The instrument is found to exhibit some high frequency signal loss, with a half-power frequency of ≈1 Hz, but a correction based on an empirically determined instrument response function is presented. Standard micrometeorological assumptions of steady state and horizontal uniformity are found to be appropriate for DMS flux measurement, but rapid changes in mean DMS mixing ratio may serve as a warning that measured flux does not represent the true surface flux. In addition, bias in surface flux estimates arising from the flux divergence is not generally significant in the surface layer, but under conditions of lowered inversion and high flux may become so. The effects of error in motion corrections and of vertical motion within the surface layer concentration gradient are discussed and the estimated maximum error from these effects is ≤18%.


2018 ◽  
Vol 58 (6) ◽  
pp. 998
Author(s):  
M. J. Harvey ◽  
S. E. Nichol ◽  
A. M. S. McMillan ◽  
R. J. Martin ◽  
M. J. Evans ◽  
...  

We have developed a high-precision micrometeorological system capable of measuring emissions of nitrous oxide (N2O) from up to four adjacent pasture plots. The system can be used to compare the influence of environmental factors and management practice on N2O emissions at the paddock scale. The system is capable of determining a minimum detectable N2O difference of the order of 40 pmol/mol, with an ability to resolve flux differences among plots of ~26 µg (N2O-N)/m2.h. So as to independently verify the emission estimates of the micrometeorological system, we developed a calibrated N2O-release system and compared known release rates with the micrometeorological flux estimates. Adjustable release rates up to the equivalent average surface flux of ~500 µg (N2O-N)/m2.h were achieved using mass flow-controlled input of pure N2O in a compressed air stream over two 1.5-ha plots upwind of flux-measurement masts. The comparison of network release rate with measured emission rate was quite variable and complicated by a significant and varying background emissions of N2O from the soil. For optimal steady-wind cases, the ratio of uncorrected measured flux to known release, including the estimated background, was of the order of 0.4–0.5; this ratio is likely to be influenced by the turbulent Schmidt number. Flux estimates for uncorrected flux gradient and WindTrax backward Lagrangian Stochastic method (which includes Schmidt correction) agreed well with a ratio of 0.54. The experiment highlighted the need for accurate estimates of gas eddy diffusivity in the micrometeorological gradient or difference-based flux measurement of N2O.


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