Institution
Climate Monitoring and Diagnostics Laboratory
About: Climate Monitoring and Diagnostics Laboratory is a based out in . It is known for research contribution in the topics: Aerosol & Stratosphere. The organization has 107 authors who have published 263 publications receiving 26434 citations.
Topics: Aerosol, Stratosphere, Ozone depletion, Ozone layer, Polar vortex
Papers published on a yearly basis
Papers
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TL;DR: In this paper, a 3-D transport model was used to predict a decrease in CH4 emissions of ∼10 Tg CH4 from north of 50°N in the early 1990s, which may have accelerated the global methane budget towards steady state.
Abstract: [1] The globally-averaged atmospheric methane abundance determined from an extensive network of surface air sampling sites was constant at ∼1751 ppb from 1999 through 2002. Assuming that the methane lifetime has been constant, this implies that during this 4-year period the global methane budget has been at steady state. We also observed a significant decrease in the difference between northern and southern polar zonal annual averages of CH4 from 1991 to 1992. Using a 3-D transport model, we show that this change is consistent with a decrease in CH4 emissions of ∼10 Tg CH4 from north of 50°N in the early-1990s. This decrease in emissions may have accelerated the global methane budget towards steady state. Based on current knowledge of the global methane budget and how it has changed with time, it is not possible to tell if the atmospheric methane burden has peaked, or if we are only observing a persistent, but temporary pause in its increase.
455 citations
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TL;DR: In this article, the authors present an analysis of methane measurements from a global air sampling network that suggests that, assuming constant OH concentration, global annual methane emissions have remained nearly constant during the period 1984-96, and that the decreasing growth rate in atmospheric methane reflects the approach to a steady state on a timescale comparable to methane's atmospheric lifetime.
Abstract: The global atmospheric methane burden has more than doubled since pre-industrial times1,2, and this increase is responsible for about 20% of the estimated change in direct radiative forcing due to anthropogenic greenhouse-gas emissions. Research into future climate change and the development of remedial environmental policies therefore require a reliable assessment of the long-term growth rate in the atmospheric methane load. Measurements have revealed that although the global atmospheric methane burden continues to increase2 with significant interannual variability3,4, the overall rate of increase has slowed2,5. Here we present an analysis of methane measurements from a global air sampling network that suggests that, assuming constant OH concentration, global annual methane emissions have remained nearly constant during the period 1984–96, and that the decreasing growth rate in atmospheric methane reflects the approach to a steady state on a timescale comparable to methane's atmospheric lifetime. If the global methane sources and OH concentration continue to remain constant, we expect average methane mixing ratios to increase slowly from today's 1,730 nmol mol−1 to ∼1,800 nmol mol−1, with little change in the contribution of methane to the greenhouse effect.
419 citations
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State University of New York System1, Langley Research Center2, Lawrence Livermore National Laboratory3, Climate Monitoring and Diagnostics Laboratory4, Bureau of Meteorology5, National Center for Atmospheric Research6, Pennsylvania State University7, European Centre for Medium-Range Weather Forecasts8, University of California, San Diego9
TL;DR: Collocated satellite and surface measurements of solar radiation at five geographically diverse locations showed significant solar absorption by clouds, resulting in about 25 watts per square meter more global-mean absorption by the cloudy atmosphere than predicted by theoretical models.
Abstract: There has been a long history of unexplained anomalous absorption of solar radiation by clouds. Collocated satellite and surface measurements of solar radiation at five geographically diverse locations showed significant solar absorption by clouds, resulting in about 25 watts per square meter more global-mean absorption by the cloudy atmosphere than predicted by theoretical models. It has often been suggested that tropospheric aerosols could increase cloud absorption. But these aerosols are temporally and spatially heterogeneous, whereas the observed cloud absorption is remarkably invariant with respect to season and location. Although its physical cause is unknown, enhanced cloud absorption substantially alters our understanding of the atmosphere's energy budget.
406 citations
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TL;DR: The Southern Hemisphere Additional Ozonesondes (SHADOZ) project as mentioned in this paper collected ozone profiles from 10 southern hemisphere tropical and subtropical stations and compared column-integrated total ozone from sondes with the Earth-Probe/Total Ozone Mapping Spectrometer (TOMS) satellite and ground-based instruments.
Abstract: [1] A network of 10 southern hemisphere tropical and subtropical stations, designated the Southern Hemisphere Additional Ozonesondes (SHADOZ) project and established from operational sites, provided over 1000 ozone profiles during the period 1998–2000. Balloon-borne electrochemical concentration cell (ECC) ozonesondes, combined with standard radiosondes for pressure, temperature, and relative humidity measurements, collected profiles in the troposphere and lower to midstratosphere at: Ascension Island; Nairobi, Kenya; Irene, South Africa; Reunion Island; Watukosek, Java; Fiji; Tahiti; American Samoa; San Cristobal, Galapagos; and Natal, Brazil. The archived data are available at: 〈http://croc.gsfc.nasa.gov/shadoz〉.1 In this paper, uncertainties and accuracies within the SHADOZ ozone data set are evaluated by analyzing: (1) imprecisions in profiles and in methods of extrapolating ozone above balloon burst; (2) comparisons of column-integrated total ozone from sondes with total ozone from the Earth-Probe/Total Ozone Mapping Spectrometer (TOMS) satellite and ground-based instruments; and (3) possible biases from station to station due to variations in ozonesonde characteristics. The key results are the following: (1) Ozonesonde precision is 5%. (2) Integrated total ozone column amounts from the sondes are usually to within 5% of independent measurements from ground-based instruments at five SHADOZ sites and overpass measurements from the TOMS satellite (version 7 data). (3) Systematic variations in TOMS-sonde offsets and in ground-based-sonde offsets from station to station reflect biases in sonde technique as well as in satellite retrieval. Discrepancies are present in both stratospheric and tropospheric ozone. (4) There is evidence for a zonal wave-one pattern in total and tropospheric ozone, but not in stratospheric ozone.
401 citations
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TL;DR: Aerosol data consisting of condensation nuclei (CN) counts, black carbon (BC) mass, aerosol light scattering (SC), and aerosol optical depth (AOD) measured at Barrow, Alaska from 1977 to 1994 have been analyzed by three-way positive matrix factorization (PMF3) by pooling all of the different data into one large threeway array.
346 citations
Authors
Showing all 107 results
Name | H-index | Papers | Citations |
---|---|---|---|
Edward J. Dlugokencky | 72 | 207 | 27280 |
Samuel J. Oltmans | 70 | 192 | 16132 |
Stephen A. Montzka | 69 | 219 | 19055 |
John A. Ogren | 68 | 197 | 16355 |
Pieter P. Tans | 63 | 163 | 19286 |
John B. Miller | 54 | 168 | 13703 |
Anna M. Michalak | 50 | 188 | 9646 |
Arlyn E. Andrews | 49 | 143 | 8024 |
Holger Vömel | 48 | 166 | 7707 |
Michael H. Bergin | 47 | 141 | 7749 |
Terry Deshler | 46 | 182 | 7438 |
Joyce M. Harris | 45 | 92 | 6285 |
Wouter Peters | 44 | 141 | 11055 |
Anne Jefferson | 44 | 82 | 4932 |
Bryan J. Johnson | 44 | 94 | 5840 |