Global and regional importance of the direct dust-climate feedback.

Feedbacks between the global dust cycle and the climate system might have amplified past climate changes. Yet, it remains unclear what role the dust-climate feedback will play in future anthropogenic climate change. Here, we estimate the direct dust-climate feedback, arising from changes in the dust direct radiative effect (DRE), using a simple theoretical framework that combines constraints on the dust DRE with a series of climate model results. We find that the direct dust-climate feedback is likely in the range of -0.04 to +0.02 Wm -2 K-1, such that it could account for a substantial fraction of the total aerosol feedbacks in the climate system. On a regional scale, the direct dust-climate feedback is enhanced by approximately an order of magnitude close to major source regions. This suggests that it could play an important role in shaping the future climates of Northern Africa, the Sahel, the Mediterranean region, the Middle East, and Central Asia

Development of a 3-dimensional chemical transport model based on observed winds and use in inverse modeling of the sources of CCl₃F

Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Earth, Atmospheric, and Planetary Sciences, 1996.Includes bibliographical references (p. 193-199).Natalie Marie Mahowald.Ph.D

Equatorial Upwelling Enhances Nitrogen Fixation in the Atlantic Ocean

Surface waters in upwelling regions are thought to be nutrient rich and hence inhibit nitrogen fixation (diazotrophy) because diazotrophs can preferentially assimilate nitrate and ammonia instead of expending energy to fix dinitrogen. We found average nitrogen fixation rates to be two to seven times higher in the surface waters of the upwelling region of the eastern equatorial Atlantic than typically measured here during non-upwelling periods. We posit that in this region, low nitrate-phosphate ratio waters are upwelled, and an initial bloom of non-diazotrophic phytoplankton removes recently upwelled nitrate. Thereby, diazotrophy is fuelled by residual phosphate and by a combination of aeolian and upwelled sources of iron. Annually, we estimate that approximately 47 Gmol of new nitrogen is introduced by diazotrophy in upwelled waters alone and 195 Gmol N is fixed in the equatorial Atlantic region. Our findings challenge the paradigm that the highest nitrogen fixation rates occur in oligotrophic gyres and instead provide evidence of its importance in upwelling regimes where phosphate- and iron-rich waters rich are upwelled

Aerosol-Climate Interactions During the Last Glacial Maximum

International audience; Purpose of Review: Natural archives are imprinted with signs of the past variability of some aerosol species in connection to major climate changes. In certain cases, it is possible to use these paleo-observations as a quantitative tool for benchmarking climate model simulations. Where are we on the path to use observations and models in connection to define an envelope on aerosol feedback onto climate? Recent Findings: On glacial-interglacial time scales, the major advances in our understanding refer to mineral dust, in terms of quantifying its global mass budget, as well as in estimating its direct impacts on the atmospheric radiation budget and indirect impacts on the oceanic carbon cycle. Summary: Even in the case of dust, major uncertainties persist. More detailed observational studies and model intercomparison experiments such as in the Paleoclimate Modelling Intercomparison Project phase 4 will be critical in advancing the field. The inclusion of new processes such as cloud feedbacks and studies focusing on other aerosol species are also envisaged

Impact of variable air-sea O2 and CO2 fluxes on atmospheric potential oxygen (APO) and land-ocean carbon sink partitioning

© 2008 Author(s). This article is distributed under the terms of the Creative Commons Attribution 3.0 License. The definitive version was published in Biogeosciences 5 (2008): 875-899, doi:10.5194/bg-5-875-2008A three dimensional, time-evolving field of atmospheric potential oxygen (APO ~O2/N2+CO2) was estimated using surface O2, N2 and CO2 fluxes from the WHOI ocean ecosystem model to force the MATCH atmospheric transport model. Land and fossil carbon fluxes were also run in MATCH and translated into O2 tracers using assumed O2:CO2 stoichiometries. The modeled seasonal cycles in APO agree well with the observed cycles at 13 global monitoring stations, with agreement helped by including oceanic CO2 in the APO calculation. The modeled latitudinal gradient in APO is strongly influenced by seasonal rectifier effects in atmospheric transport. An analysis of the APO-vs.-CO2 mass-balance method for partitioning land and ocean carbon sinks was performed in the controlled context of the MATCH simulation, in which the true surface carbon and oxygen fluxes were known exactly. This analysis suggests uncertainty of up to ±0.2 PgC in the inferred sinks due to variability associated with sparse atmospheric sampling. It also shows that interannual variability in oceanic O2 fluxes can cause large errors in the sink partitioning when the method is applied over short timescales. However, when decadal or longer averages are used, the variability in the oceanic O2 flux is relatively small, allowing carbon sinks to be partitioned to within a standard deviation of 0.1 Pg C/yr of the true values, provided one has an accurate estimate of long-term mean O2 outgassing.We acknowledge the support of NASA grant NNG05GG30G and NSF grant ATM0628472

Are the impacts of land use on warming underestimated in climate policy?

© The Author(s), 2017. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Environmental Research Letters 12 (2017): 094016, doi:10.1088/1748-9326/aa836d.While carbon dioxide emissions from energy use must be the primary target of climate change mitigation efforts, land use and land cover change (LULCC) also represent an important source of climate forcing. In this study we compute time series of global surface temperature change separately for LULCC and non-LULCC sources (primarily fossil fuel burning), and show that because of the extra warming associated with the co-emission of methane and nitrous oxide with LULCC carbon dioxide emissions, and a co-emission of cooling aerosols with non-LULCC emissions of carbon dioxide, the linear relationship between cumulative carbon dioxide emissions and temperature has a two-fold higher slope for LULCC than for non-LULCC activities. Moreover, projections used in the Intergovernmental Panel on Climate Change (IPCC) for the rate of tropical land conversion in the future are relatively low compared to contemporary observations, suggesting that the future projections of land conversion used in the IPCC may underestimate potential impacts of LULCC. By including a ‘business as usual’ future LULCC scenario for tropical deforestation, we find that even if all non-LULCC emissions are switched off in 2015, it is likely that 1.5 ◦C of warming relative to the preindustrial era will occur by 2100. Thus, policies to reduce LULCC emissions must remain a high priority if we are to achieve the low to medium temperature change targets proposed as a part of the Paris Agreement. Future studies using integrated assessment models and other climate simulations should include more realistic deforestation rates and the integration of policy that would reduce LULCC emissions.We would like to acknowledge the support from grants NSF-ATM1049033, NSF-CCF-1522054, NSFAGS- 1048827 and DOE-SC0016362, DOE Office of Science Biogeochemical Cycles Feedbacks and ACME Science Focus Areas as well as assistance from the Atkinson Center for a Sustainable Futur

Exploring the sensitivity of interannual basin-scale air-sea CO2 fluxes to variability in atmospheric dust deposition using ocean carbon cycle models and atmospheric CO2 inversions

Author Posting. © American Geophysical Union, 2007. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research 112 (2007): G02012, doi:10.1029/2006JG000236.Estimates of sources/sinks of carbon dioxide (CO2) at the Earth's surface are commonly made using atmospheric CO2 inverse modeling, terrestrial and oceanic biogeochemical modeling, and inventory-based studies. In this study, we compare sea-air CO2 fluxes from the Time-Dependent Inverse (TDI) atmosphere model and the marine Biogeochemical Elemental Cycling (BEC) model to study the processes involved in ocean carbon cycling at subbasin scales. A dust generation and transport model, based on analyzed meteorology and terrestrial vegetation cover, is also used to estimate the interannual variability in dust and iron deposition to different ocean basins. Overall, a fairly good agreement is established between the TDI and BEC model results for the net annual patterns and seasonal cycle of sea-air CO2 exchange. Sensitivity studies with the ocean biogeochemical model using increased or reduced atmospheric iron inputs indicate the relative sensitivity of air-sea CO2 exchange. The simulated responses to changes in iron inputs are not instantaneous (peak response after ∼2−3 years). The TDI model derived seasonal cycles for the Southern Ocean (South Atlantic) are better matched by the BEC model by increasing (decreasing) iron inputs through atmospheric aerosols. Our results suggest that some of the interannual variability in TDI model air-sea CO2 fluxes during the past decade may be explainable by dust variability that relaxes/increases iron limitation in high-nitrate, low-chlorophyll (HNLC) ocean regions.S. C. Doney and N. Mahowald acknowledge support from NASA grant NNG05GG30G. J. K. Moore was funded by NSF grant OCE-0452972

Constraining the Atmospheric Limb of the Plastic Cycle

Plastic pollution is one of the most pressing environmental and social issues of the 21st century. Recent work has highlighted the atmosphere’s role in transporting microplastics to remote locations [S. Allen et al., Nat. Geosci. 12, 339 (2019) and J. Brahney, M. Hallerud, E. Heim, M. Hahnenberger, S. Sukumaran, Science 368, 1257–1260 (2020)]. Here, we use in situ observations of microplastic deposition combined with an atmospheric transport model and optimal estimation techniques to test hypotheses of the most likely sources of atmospheric plastic. Results suggest that atmospheric microplastics in the western United States are primarily derived from secondary re-emission sources including roads (84%), the ocean (11%), and agricultural soil dust (5%). Using our best estimate of plastic sources and modeled transport pathways, most continents were net importers of plastics from the marine environment, underscoring the cumulative role of legacy pollution in the atmospheric burden of plastic. This effort uses high-resolution spatial and temporal deposition data along with several hypothesized emission sources to constrain atmospheric plastic. Akin to global biogeochemical cycles, plastics now spiral around the globe with distinct atmospheric, oceanic, cryospheric, and terrestrial residence times. Though advancements have been made in the manufacture of biodegradable polymers, our data suggest that extant nonbiodegradable polymers will continue to cycle through the earth’s systems. Due to limited observations and understanding of the source processes, there remain large uncertainties in the transport, deposition, and source attribution of microplastics. Thus, we prioritize future research directions for understanding the plastic cycle