Disjunct Eddy Covariance Method Research Articles

InnFLUX – an open-source code for conventional and disjunct eddy covariance analysis of trace gas measurements: an urban test case

Abstract. We describe and test a new versatile software tool for processing eddy covariance and disjunct eddy covariance flux data. We present an evaluation based on urban non-methane volatile organic compound (NMVOC) measurements using a proton transfer reaction quadrupole interface time-of-flight mass spectrometer (PTR-QiTOF-MS) at the Innsbruck Atmospheric Observatory. The code is based on MATLAB® and can be easily configured to process high-frequency, low-frequency and disjunct data. It can be applied to a wide range of analytical setups for NMVOC and other trace gas measurements, and is tailored towards the application of noisy data, where lag time corrections become challenging. Several corrections and quality control routines are implemented to obtain the most reliable results. The software is open source, so it can be extended and adjusted to specific purposes. We demonstrate the capabilities of the code based on a large urban dataset collected in Innsbruck, Austria, where three-dimensional winds and ambient concentrations of NMVOCs and auxiliary trace gases were sampled with high temporal resolution above an urban canopy. Concomitant measurements of 12C and 13C isotopic NMVOC fluxes allow testing algorithms used for determination of flux limits of detection (LOD) and lag time analysis. We use the high-frequency NMVOC dataset to generate a set of disjunct data and compare these results with the true eddy covariance method. The presented analysis allows testing the theory of disjunct eddy covariance (DEC) in an urban environment. Our findings confirm that the disjunct eddy covariance method can be a reliable tool, even in complex urban environments when fast sensors are not available, but that the increase in random error impedes the ability to detect small fluxes due to higher flux LODs.

Biogenic volatile organic compound emissions during BEARPEX 2009 measured by eddy covariance and flux–gradient similarity methods

Abstract. The Biosphere Effects on AeRosols and Photochemistry EXperiment (BEARPEX) took place in Blodgett Forest, a Ponderosa pine forest in the Sierra Nevada of California, USA, during summer 2009. We deployed a proton transfer reaction–quadrupole mass spectrometer (PTR-QMS) to measure fluxes and concentrations of biogenic volatile organic compounds (BVOCs). Eighteen ion species, including the major BVOC expected at the site, were measured sequentially at 5 heights to observe their vertical gradient from the forest floor to above the canopy. Fluxes of the 3 dominant BVOCs methanol, 2-Methyl-3-butene-2-ol (MBO), and monoterpenes were measured above the canopy by the disjunct eddy covariance (EC) method. Canopy-scale fluxes were also determined by the flux–gradient similarity method (K-theory). A universal K (Kuniv) was determined as the mean of individual K's calculated from the measured fluxes divided by vertical gradients for methanol, MBO, and monoterpenes. This Kuniv was then multiplied by the gradients of each observed ion species to compute their fluxes. The flux–gradient similarity method showed very good agreement with the disjunct EC method. Fluxes are presented for all measured species and compared to historical measurements from the same site, and used to test emission algorithms used to model fluxes at the regional scale. MBO was the dominant emission observed, followed by methanol, monoterpenes, acetone, and acetaldehyde. The flux–gradient similarity method is shown to be tenable, and we recommend its use, especially in experimental conditions when fast measurement of BVOC species is not available.

Role of de novo biosynthesis in ecosystem scale monoterpene emissions from a boreal Scots pine forest

Abstract. Monoterpene emissions from Scots pine have traditionally been assumed to originate as evaporation from specialized storage pools. More recently, the significance of de novo emissions, originating directly from monoterpene biosynthesis, has been recognized. To study the role of biosynthesis at the ecosystem scale, we measured monoterpene emissions from a Scots pine dominated forest in southern Finland using the disjunct eddy covariance method combined with proton transfer reaction mass spectrometry. The interpretation of the measurements was based on a correlation analysis and a hybrid emission algorithm describing both de novo and pool emissions. During the measurement period May–August 2007, the monthly medians of daytime emissions were 200, 290, 180, and 200 μg m−2 h−1. The emissions were partly light dependent, probably due to de novo biosynthesis. The emission potential for both de novo and pool emissions exhibited a decreasing summertime trend. The ratio of the de novo emission potential to the total emission potential varied between 30 % and 46 %. Although the monthly changes were not significant, the ratio always differed statistically from zero, suggesting that the role of de novo biosynthesis was observable. Given the uncertainties in this study, we conclude that more accurate estimates of the contribution of de novo emissions are required for improving monoterpene emission algorithms for Scots pine dominated forests.

BVOC fluxes above mountain grassland

Grasslands comprise natural tropical savannah over managed temperate fields to tundra and cover one quarter of the Earth's land surface. Plant growth, maintenance and decay result in volatile organic compound (VOCs) emissions to the atmosphere. Furthermore, biogenic VOCs (BVOCs) are emitted as a consequence of various environmental stresses including cutting and drying during harvesting. Fluxes of BVOCs were measured with a proton-transfer-reaction-mass-spectrometer (PTR-MS) over temperate mountain grassland in Stubai Valley (Tyrol, Austria) over one growing season (2008). VOC fluxes were calculated from the disjunct PTR-MS data using the virtual disjunct eddy covariance method and the gap filling method. Methanol fluxes obtained with the two independent flux calculation methods were highly correlated (y = 0.95×-0.12, R2 = 0.92). Methanol showed strong daytime emissions throughout the growing season - with maximal values of 9.7 nmol m-2 s-1, methanol fluxes from the growing grassland were considerably higher at the beginning of the growing season in June compared to those measured during October (2.5 nmol m-2 s-1). Methanol was the only component that exhibited consistent fluxes during the entire growing periods of the grass. The cutting and drying of the grass increased the emissions of methanol to up to 78.4 nmol m-2 s-1. In addition, emissions of acetaldehyde (up to 11.0 nmol m-2 s-1), and hexenal (leaf aldehyde, up to 8.6 nmol m-2 s-1) were detected during/after harvesting.

Direct determination of highly size-resolved turbulent particle fluxes with the disjunct eddy covariance method and a 12 – stage electrical low pressure impactor

Abstract. During summer 2007, turbulent vertical particle mass and number fluxes were measured for a period of 98 days near the city centre of Münster in north-west Germany. For this purpose, a valve controlled disjunct eddy covariance system was mounted at 65 m a.g.l. on a military radio tower. The concentration values for 11 size bins with aerodynamic diameters (D50) from 0.03 to 10 μm were measured with an electrical low pressure impactor. After comparison with other fluxes obtained from 10 Hz measurements with the classical eddy covariance method, the loss of information concerning high frequent parts of the flux could be stated as negligible. The results offer an extended insight in the turbulent atmospheric exchange of aerosol particles by highly size-resolved particle fluxes covering 11 size bins and show that the city of Münster acts as a relevant source for aerosol particles. Significant differences occur between the fluxes of the various particle size classes. While the total particle number flux shows a pattern which is strictly correlated to the diurnal course of the turbulence regime and the traffic intensity, the total mass flux exhibits a single minimum in the evening hours when coarse particles start to deposit. As a result, a mean mass deposition of about 10 mg m−2 per day was found above the urban test site, covering the aerosol size range from 40 nm to 2.0 μm. By contrast, the half-hourly total number fluxes accumulated over the lower ELPI stages range from −4.29×107 to +1.44×108 particles m−2 s−1 and are clearly dominated by the sub-micron particle fraction of the impactor stages with diameters between 40 nm and 320 nm. The averaged number fluxes of particles with diameters between 2.0 and 6.4 μm show lower turbulent dynamics during daytime and partially remarkably high negative fluxes with mean deposition velocities of 2×10−3 m s−1 that appear temporary during noontime and in the evening hours.