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Paul O. Wennberg

Researcher at California Institute of Technology

Publications -  421
Citations -  35598

Paul O. Wennberg is an academic researcher from California Institute of Technology. The author has contributed to research in topics: Total Carbon Column Observing Network & Isoprene. The author has an hindex of 96, co-authored 398 publications receiving 30122 citations. Previous affiliations of Paul O. Wennberg include National Oceanic and Atmospheric Administration & Harvard University.

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Sources of variations in total column carbon dioxide

TL;DR: In this paper, the authors use a general circulation model with a variety of prescribed carbon fluxes to investigate how variations in (CO 2 ) arise on diurnal and seasonal scales.
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Space‐based near‐infrared CO2 measurements: Testing the Orbiting Carbon Observatory retrieval algorithm and validation concept using SCIAMACHY observations over Park Falls, Wisconsin

Abstract: Space-based measurements of reflected sunlight in the near-infrared (NIR) region promise to yield accurate and precise observations of the global distribution of atmospheric CO_2. The Orbiting Carbon Observatory (OCO) is a future NASA mission, which will use this technique to measure the column-averaged dry air mole fraction of CO_2 (X_(CO)_2) with the precision and accuracy needed to quantify CO_2 sources and sinks on regional scales (∼1000 × 1000 km^2) and to characterize their variability on seasonal timescales. Here, we have used the OCO retrieval algorithm to retrieve (X_(CO)_2) and surface pressure from space-based Scanning Imaging Absorption Spectrometer for Atmospheric Chartography (SCIAMACHY) measurements and from coincident ground-based Fourier transform spectrometer (FTS) measurements of the O_2 A band at 0.76 μm and the 1.58 μm CO_2 band for Park Falls, Wisconsin. Even after accounting for a systematic error in our representation of the O_2 absorption cross sections, we still obtained a positive bias between SCIAMACHY and FTS (X_(CO)_2) retrievals of ∼3.5%. Additionally, the retrieved surface pressures from SCIAMACHY systematically underestimate measurements of a calibrated pressure sensor at the FTS site. These findings lead us to speculate about inadequacies in the forward model of our retrieval algorithm. By assuming a 1% intensity offset in the O_2 A band region for the SCIAMACHY (X_(CO)_2) retrieval, we significantly improved the spectral fit and achieved better consistency between SCIAMACHY and FTS (X_(CO)_2) retrievals. We compared the seasonal cycle of (X_(CO)_2)at Park Falls from SCIAMACHY and FTS retrievals with calculations of the Model of Atmospheric Transport and Chemistry/Carnegie-Ames-Stanford Approach (MATCH/CASA) and found a good qualitative agreement but with MATCH/CASA underestimating the measured seasonal amplitude. Furthermore, since SCIAMACHY observations are similar in viewing geometry and spectral range to those of OCO, this study represents an important test of the OCO retrieval algorithm and validation concept using NIR spectra measured from space. Finally, we argue that significant improvements in precision and accuracy could be obtained from a dedicated CO_2 instrument such as OCO, which has much higher spectral and spatial resolutions than SCIAMACHY. These measurements would then provide critical data for improving our understanding of the carbon cycle and carbon sources and sinks.
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New constraints on Northern Hemisphere growing season net flux

TL;DR: The authors used the column-averaged dry molar mixing ratio of CO 2 above both Park Falls, Wisconsin and Kitt Peak, Arizona, together with partial columns derived from aircraft profiles over Eurasia and North America to estimate the seasonal integral of net ecosystem exchange (NEE) between the atmosphere and the terrestrial biosphere in the Northern Hemisphere.
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On the Sources of Methane to the Los Angeles Atmosphere

TL;DR: Emissions from natural gas seeps as well as those associated with petroleum production, both of which are poorly known, will reduce the inferred contribution of the natural gas infrastructure to the total CH(4) emissions, potentially significantly.