Large volcanic eruptions drive significant climate perturbations through major anomalies in radiative fluxes and the resulting widespread cooling of the surface and upper ocean. Recent studies suggest that these eruptions also drive important variability in air‐sea carbon and oxygen fluxes. By simulating the Earth system using two initial‐condition large ensembles, with and without the aerosol forcing associated with the Mt. Pinatubo eruption in June 1991, we isolate the impact of this volcanic event on physical and biogeochemical properties of the ocean. The Mt. Pinatubo eruption forced significant anomalies in surface fluxes and the ocean interior inventories of heat, oxygen, and carbon. Pinatubo‐driven changes persist for multiple years in the upper ocean and permanently modify the ocean's heat, oxygen, and carbon inventories. Positive anomalies in oxygen concentrations emerge immediately post‐eruption and penetrate into the deep ocean. In contrast, carbon anomalies intensify in the upper ocean over several years post‐eruption, and are largely confined to the upper 150 m. In the tropics and northern high latitudes, the change in oxygen is dominated by surface cooling and subsequent ventilation to mid‐depths, while the carbon anomaly is associated with solubility changes and eruption‐generated El Niño—Southern Oscillation variability. We do not find significant impact of Pinatubo on oxygen or carbon fluxes in the Southern Ocean; but this may be due to Southern Hemisphere aerosol forcing being underestimated in Community Earth System Model 1 simulations.
Decreases in stratospheric NOxassociated with enhanced aerosol have been observed after large volcanic eruptions, for example, after the eruption of Mount Pinatubo in 1991. While the 1991 Mount Pinatubo eruption was the last large explosive eruption, recent studies have shed light on the impacts of moderate‐sized eruptions since the year 2000 on the global stratospheric aerosol budget. We use an ensemble of simulations from a coupled climate‐chemistry model to quantify and analyze changes in NO and NO2(NOx), N2O5, HNO3, ClO, and ClONO2during periods of increased stratospheric volcanic aerosol concentrations since 2000. By using an ensemble approach, we are able to distinguish forced responses from internal variability. We also compare the model ensemble results to satellite measurements of these changes in atmospheric composition, including measurements from the Optical Spectrograph and Infrared Imaging Spectrometer on the Odin satellite and the Aura Microwave Limb Sounder. We find decreases in stratospheric NOxconcentrations up to 20 hPa, consistent with increases in stratospheric HNO3concentrations. The HNO3perturbations also extend higher, up to 5 hPa, associated with periods of increased volcanic aerosol concentrations in both model simulations and observations, though correlations with volcanic aerosol are considerably higher in the model simulations. The model simulates increases in ClO at altitudes and magnitudes similar to the NOxreductions, but this response is below the detectable limit in the available observations (100 pptv). We also demonstrate the value of accounting for transport‐related anomalies of atmospheric trace gases by regression onto N2O anomalies.
more » « less- NSF-PAR ID:
- 10445729
- Publisher / Repository:
- DOI PREFIX: 10.1029
- Date Published:
- Journal Name:
- Journal of Geophysical Research: Atmospheres
- Volume:
- 124
- Issue:
- 17-18
- ISSN:
- 2169-897X
- Page Range / eLocation ID:
- p. 10283-10303
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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