159 research outputs found

    Methane observations from the Greenhouse Gases Observing SATellite: Comparison to ground‐based TCCON data and model calculations

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    We report new short-wave infrared (SWIR) column retrievals of atmospheric methane (X_(CH4)) from the Japanese Greenhouse Gases Observing SATellite (GOSAT) and compare observed spatial and temporal variations with correlative ground-based measurements from the Total Carbon Column Observing Network (TCCON) and with the global 3-D GEOS-Chem chemistry transport model. GOSAT X_(CH4) retrievals are compared with daily TCCON observations at six sites between April 2009 and July 2010 (Bialystok, Park Falls, Lamont, Orleans, Darwin and Wollongong). GOSAT reproduces the site-dependent seasonal cycles as observed by TCCON with correlations typically between 0.5 and 0.7 with an estimated single-sounding precision between 0.4–0.8%. We find a latitudinal-dependent difference between the X_(CH4) retrievals from GOSAT and TCCON which ranges from 17.9 ppb at the most northerly site (Bialystok) to −14.6 ppb at the site with the lowest latitude (Darwin). We estimate that the mean smoothing error difference included in the GOSAT to TCCON comparisons can account for 15.7 to 17.4 ppb for the northerly sites and for 1.1 ppb at the lowest latitude site. The GOSAT X_(CH4) retrievals agree well with the GEOS-Chem model on annual (August 2009 – July 2010) and monthly timescales, capturing over 80% of the zonal variability. Differences between model and observed X_(CH4) are found over key source regions such as Southeast Asia and central Africa which will be further investigated using a formal inverse model analysis

    Spatial resolution of tropical terrestrial CO2 fluxes inferred using space-borne column CO2 sampled in different earth orbits: the role of spatial error correlations

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    We use realistic numerical experiments to assess the sensitivity of 8-day CO<sub>2</sub> flux estimates, inferred from space-borne short-wave infrared measurements of column-averaged CO<sub>2</sub> dry air mixing ratio <i>X</i><sub>CO<sub>2</sub></sub>, to the choice of Earth observing orbit. We focus on three orbits: (1) a low-inclination circular orbit used by the NASA Tropical Rainfall Measuring Mission (TRMM); (2) a sun-synchronous orbit used by the Japanese Greenhouse Gases Observing SATellite (GOSAT) and proposed for the NASA Orbiting Carbon Observatory (OCO-2) instrument; and (3) a precessing orbit used by the International Space Station (ISS). For each orbit, we assume an instrument based on the specification of the OCO-2; for GOSAT we use the relevant instrument specification. Sun-synchronous orbits offer near global coverage within a few days but have implications for the density of clear-sky measurements. The TRMM and ISS orbits intensively sample tropical latitudes, with sun-lit clear-sky measurements evenly distributed between a.m./p.m. For a specified spatial resolution for inferred fluxes, we show there is a critical number of measurements beyond which there is a disproportionately small decrease in flux uncertainty. We also show that including spatial correlations for measurements and model errors (of length 300 km) reduces the effectiveness of high measurement density for flux estimation, as expected, and so should be considered when deciding sampling strategies. We show that cloud-free data from the TRMM orbit generally can improve the spatial resolution of CO<sub>2</sub> fluxes achieved by OCO-2 over tropical South America, for example, from 950 km to 630 km, and that combining data from these low-inclination and sun-synchronous orbits have the potential to reduce this spatial length further. Decreasing the length of the error correlations to 50 km, reflecting anticipated future improvements to transport models, results in CO<sub>2</sub> flux estimates on spatial scales that approach those observed by regional aircraft

    Environmental effects of James River sewage treatment plant outfall construction

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    In the spring of 1975 the Institute began a program to determine whether significant environmental changes would occur in the area of the new James River Plant outfall that might be related to its construction and/or initial operation. Parameters measured in the study were benthic animal and oyster populations, coliform levels and chlorine residuals. The primary emphasis of the study centered on the estimation of the impact of the construction activity on shellfish beds in the area. The results of the investigation are presented in three segments, the first dealing with shellfish populations, the second with other benthic animals and the third with coliforms and chlorine. Section I. Environmental Effects of James River Sewage Treatment Plant Outfall Construction on Oyster Beds in the James River by Dexter S. Haven and Paul C . Kendall Section II. Environmental Effects of the James River Sewage Treatment Plant Outfall Construction: Soft Bottom Macrobenthos by Robert J. Diaz and Donald F. Boesch Section III. Water Quality in the Vicinity of James River Sewage Treatment Plant Outfall by Michael E. Bende

    An increase in methane emissions from tropical Africa between 2010 and 2016 inferred from satellite data

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    Emissions of methane (CH4) from tropical ecosystems, and how they respond to changes in climate, represent one of the biggest uncertainties associated with the global CH4 budget. Historically, this has been due to the dearth of pan-tropical in situ measurements, which is particularly acute in Africa. By virtue of their superior spatial coverage, satellite observations of atmospheric CH4 columns can help to narrow down some of the uncertainties in the tropical CH4 emission budget. We use proxy column retrievals of atmospheric CH4 (XCH4) from the Japanese Greenhouse gases Observing Satellite (GOSAT) and the nested version of the GEOS-Chem atmospheric chemistry and transport model (0.5 ∘ ×0.625 ∘ ) to infer emissions from tropical Africa between 2010 and 2016. Proxy retrievals of XCH4 are less sensitive to scattering due to clouds and aerosol than full physics retrievals, but the method assumes that the global distribution of carbon dioxide (CO2) is known. We explore the sensitivity of inferred a posteriori emissions to this source of systematic error by using two different XCH4 data products that are determined using different model CO2 fields. We infer monthly emissions from GOSAT XCH4 data using a hierarchical Bayesian framework, allowing us to report seasonal cycles and trends in annual mean values. We find mean tropical African emissions between 2010 and 2016 range from 76 (74–78) to 80 (78–82) Tg yr−1, depending on the proxy XCH4 data used, with larger differences in Northern Hemisphere Africa than Southern Hemisphere Africa. We find a robust positive linear trend in tropical African CH4 emissions for our 7-year study period, with values of 1.5 (1.1–1.9) Tg yr−1 or 2.1 (1.7–2.5) Tg yr−1, depending on the CO2 data product used in the proxy retrieval. This linear emissions trend accounts for around a third of the global emissions growth rate during this period. A substantial portion of this increase is due to a short-term increase in emissions of 3 Tg yr−1 between 2011 and 2015 from the Sudd in South Sudan. Using satellite land surface temperature anomalies and altimetry data, we find this increase in CH4 emissions is consistent with an increase in wetland extent due to increased inflow from the White Nile, although the data indicate that the Sudd was anomalously dry at the start of our inversion period. We find a strong seasonality in emissions across Northern Hemisphere Africa, with the timing of the seasonal emissions peak coincident with the seasonal peak in ground water storage. In contrast, we find that a posteriori CH4 emissions from the wetland area of the Congo Basin are approximately constant throughout the year, consistent with less temporal variability in wetland extent, and significantly smaller than a priori estimates

    Estimating surface CO2 fluxes from space-borne CO2 dry air mole fraction observations using an ensemble Kalman Filter

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    We have developed an ensemble Kalman Filter (EnKF) to estimate 8-day regional surface fluxes of CO<sub>2</sub> from space-borne CO<sub>2</sub> dry-air mole fraction observations (X<sub>CO<sub>2</sub></sub>) and evaluate the approach using a series of synthetic experiments, in preparation for data from the NASA Orbiting Carbon Observatory (OCO). The 32-day duty cycle of OCO alternates every 16 days between nadir and glint measurements of backscattered solar radiation at short-wave infrared wavelengths. The EnKF uses an ensemble of states to represent the error covariances to estimate 8-day CO<sub>2</sub> surface fluxes over 144 geographical regions. We use a 12&times;8-day lag window, recognising that X<sub>CO<sub>2</sub></sub> measurements include surface flux information from prior time windows. The observation operator that relates surface CO<sub>2</sub> fluxes to atmospheric distributions of X<sub>CO<sub>2</sub></sub> includes: a) the GEOS-Chem transport model that relates surface fluxes to global 3-D distributions of CO<sub>2</sub> concentrations, which are sampled at the time and location of OCO measurements that are cloud-free and have aerosol optical depths <0.3; and b) scene-dependent averaging kernels that relate the CO<sub>2</sub> profiles to X<sub>CO<sub>2</sub></sub>, accounting for differences between nadir and glint measurements, and the associated scene-dependent observation errors. We show that OCO X<sub>CO<sub>2</sub></sub> measurements significantly reduce the uncertainties of surface CO<sub>2</sub> flux estimates. Glint measurements are generally better at constraining ocean CO<sub>2</sub> flux estimates. Nadir X<sub>CO<sub>2</sub></sub> measurements over the terrestrial tropics are sparse throughout the year because of either clouds or smoke. Glint measurements provide the most effective constraint for estimating tropical terrestrial CO<sub>2</sub> fluxes by accurately sampling fresh continental outflow over neighbouring oceans. We also present results from sensitivity experiments that investigate how flux estimates change with 1) bias and unbiased errors, 2) alternative duty cycles, 3) measurement density and correlations, 4) the spatial resolution of estimated flux estimates, and 5) reducing the length of the lag window and the size of the ensemble. At the revision stage of this manuscript, the OCO instrument failed to reach its orbit after it was launched on 24 February 2009. The EnKF formulation presented here is also applicable to GOSAT measurements of CO<sub>2</sub> and CH<sub>4</sub>

    Evaluation of wetland CH4 in the Joint UK Land Environment Simulator (JULES) land surface model using satellite observations

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    Wetlands are the largest natural source of methane. The ability to model the emissions of methane from natural wetlands accurately is critical to our understanding of the global methane budget and how it may change under future climate scenarios. The simulation of wetland methane emissions involves a complicated system of meteorological drivers coupled to hydrological and biogeochemical processes. The Joint UK Land Environment Simulator (JULES) is a process-based land surface model that underpins the UK Earth System Model (UKESM) and is capable of generating estimates of wetland methane emissions. In this study, we use GOSAT satellite observations of atmospheric methane along with the TOMCAT global 3-D chemistry transport model to evaluate the performance of JULES in reproducing the seasonal cycle of methane over a wide range of tropical wetlands. By using an ensemble of JULES simulations with differing input data and process configurations, we investigate the relative importance of the meteorological driving data, the vegetation, the temperature dependency of wetland methane production and the wetland extent. We find that JULES typically performs well in replicating the observed methane seasonal cycle. We calculate correlation coefficients to the observed seasonal cycle of between 0.58 and 0.88 for most regions; however, the seasonal cycle amplitude is typically underestimated (by between 1.8 and 19.5 ppb). This level of performance is comparable to that typically provided by state-of-the-art data-driven wetland CH4 emission inventories. The meteorological driving data are found to be the most significant factor in determining the ensemble performance, with temperature dependency and vegetation having moderate effects. We find that neither wetland extent configuration outperforms the other, but this does lead to poor performance in some regions. We focus in detail on three African wetland regions (Sudd, Southern Africa and Congo) where we find the performance of JULES to be poor and explore the reasons for this in detail. We find that neither wetland extent configuration used is sufficient in representing the wetland distribution in these regions (underestimating the wetland seasonal cycle amplitude by 11.1, 19.5 and 10.1 ppb respectively, with correlation coefficients of 0.23, 0.01 and 0.31). We employ the Catchment-based Macro-scale Floodplain (CaMa-Flood) model to explicitly represent river and floodplain water dynamics and find that these JULES-CaMa-Flood simulations are capable of providing a wetland extent that is more consistent with observations in this regions, highlighting this as an important area for future model development.</p

    Estimating global and North American methane emissions with high spatial resolution using GOSAT satellite data

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    We use 2009-2011 space-borne methane observations from the Greenhouse Gases Observing SATellite (GOSAT) to estimate global and North American methane emissions with 4° x 5° and up to 50 km x 50 km spatial resolution, respectively. GEOS-Chem and GOSAT data are first evaluated with atmospheric methane observations from surface and tower networks (NOAA/ESRL, TCCON) and aircraft (NOAA/ESRL, HIPPO), using the GEOS-Chem chemical transport model as a platform to facilitate comparison of GOSAT with in situ data. This identifies a high-latitude bias between the GOSAT data and GEOS-Chem that we correct via quadratic regression. Our global adjoint-based inversion yields a total methane source of 539 Tg a−1 with some important regional corrections to the EDGARv4.2 inventory used as a prior. Results serve as dynamic boundary conditions for an analytical inversion of North American methane emissions using radial basis functions to achieve high resolution of large sources and provide error characterization. We infer a US anthropogenic methane source of 40.2-42.7 Tg a−1, as compared to 24.9-27.0 Tg a−1 in the EDGAR and EPA bottom-up inventories, and 30.0-44.5 Tg a−1 in recent inverse studies. Our estimate is supported by independent surface and aircraft data and by previous inverse studies for California. We find that the emissions are highest in the southern-central US, the Central Valley of California, and Florida wetlands; large isolated point sources such as the US Four Corners also contribute. Using prior information on source locations, we attribute 29-44 % of US anthropogenic methane emissions to livestock, 22-31 % to oil/gas, 20 % to landfills/wastewater, and 11-15 % to coal. Wetlands contribute an additional 9.0-10.1 Tg a−1
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