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.

Validation of AERONET estimates of atmospheric solar fluxes and aerosol radiative forcing by ground-based broadband measurements

Abstract: [1] The AErosol RObotic NETwork (AERONET) estimates of instantaneous solar broadband fluxes (F) at surface have been validated through comparison with ground-based measurements of broadband fluxes at Mauna Loa Observatory (MLO) and by the Baseline Surface Radiation (BSRN) and the Solar Radiation Networks (SolRad-Net) during the period 1999–2005 and 1999–2006, respectively. The uncertainties in the calculated aerosol radiative forcing (ΔF) and radiative forcing efficiency (ΔFeff) at the bottom of the atmosphere were also assessed. The stations have been selected attempting to cover different aerosols influences and hence radiative properties: urban-industrial, biomass burning, mineral dust, background continental, maritime aerosols and free troposphere. The AERONET solar downward fluxes at surface agree with ground-based measurements in all situations, with a correlation higher than 99% whereas the relation of observed to modeled fluxes ranges from 0.98 to 1.02. Globally an overestimation of 9 ± 12 Wm−2 of solar measurements was found, whereas for MLO (clear atmosphere) the differences decrease noticeably up to 2 ± 10 Wm−2. The highest dispersion between AERONET estimates and measurements was observed in locations dominated by mineral dust and mixed aerosols types. In these locations, the F and ΔF uncertainties have shown a modest increase of the differences for high aerosol load, contrary to ΔFeff which are strongly affected by low aerosol load. Overall the discrepancies clustered within 9 ± 12 Wm−2 for ΔF and 28 ± 30 Wm−2 per unit of aerosol optical depth, τ, at 0.55 μm for ΔFeff, where the latter is given for τ(0.44 μm) ≥ 0.4. The error distributions have not shown any significant tendency with other aerosol radiative properties as well as size and shape particles.

Top-down estimate of a large source of atmospheric carbon monoxide associated with fuel combustion in Asia

Abstract: [1] Deriving robust regional estimates of the sources of chemically and radiatively important gases and aerosols to the atmosphere is challenging. Here, we focus on carbon monoxide. Using an inverse modeling methodology, we find that the source of carbon monoxide from fossil-fuel and biofuel combustion in Asia during 1994 was 350–380 Tg yr−1, which is 110–140 Tg yr−1 higher than bottom-up estimates derived using traditional inventory-based approaches. This discrepancy points to an important gap in our understanding of the human impact on atmospheric chemical composition.

Characteristics of biomass burning emission sources, transport, and chemical speciation in enhanced springtime tropospheric ozone profile over Hong Kong

Abstract: [1] Tropospheric ozone (O3) enhancements have been continuously observed over Hong Kong. We studied the O3 enhancement events and assessed their relation to the springtime O3 maximum in the lower troposphere over Hong Kong using a 6-year (1993 to 1999) ozonesonde data set. We identified the source regions of biomass burning emission, and established the chemical and transport characteristics of O3-rich air masses in the enhanced O3 profiles using satellite imagery, air trajectory and trace gas data measured on board the DC-8 aircraft during the PEM-West-B experiment. We identified a total of 39 O3 enhancement events, among which 35 events (90%) occurred from late February to May and 30 events (77%) had O3 enhancement within the 2.0–6.0 km altitude. The excess O3 in the O3-rich layers adds an additional 12% of O3 into the tropospheric O3 column and results in an overall springtime O3 maximum in the lower troposphere. Forward trajectory analysis suggests that the O3-rich air masses over Hong Kong can reach central Pacific and the western coast of North America within 10 days. Back air trajectories show that the O3-rich air masses in the enhanced profiles pass over the Southeast (SE) Asia subcontinent, where active biomass burning occurs in the O3 enhancement period. We identified the Indo-Burma region containing Burma, Laos and northern Thailand, and the Indian-Nepal region containing northern India and Nepal as the two most active regions of biomass burning emissions in the SE Asia subcontinent. Ozone and trace gas measurement on board the DC-8 aircraft revealed that O3-rich air masses are found over many parts of the tropical SE Asia and subtropical western Pacific regions and they have similar chemical characteristics. The accompanying trace gas measurements suggest that the O3-rich air masses are rich in biomass burning tracer, CH3Cl, but not the general urban emission tracers. We thus believe that the springtime O3 enhancement over Hong Kong is as a result of transport of photochemical O3 produced from biomass burning emissions from the upwind SE Asian continent. The large-scale enhancements of O3 in tropical SE Asia and the subtropical western Pacific rim that result from SE Asian biomass burning activities such as presented here thus are of atmospheric importance and deserve further research efforts.