Douglas S. Hamilton

Bio: Douglas S. Hamilton is an academic researcher from Cornell University. The author has contributed to research in topics: Aerosol & Mineral dust. The author has an hindex of 20, co-authored 35 publications receiving 1016 citations. Previous affiliations of Douglas S. Hamilton include University of Leeds & Ithaca College.

Aerosol trace metal leaching and impacts on marine microorganisms

Abstract: Metal dissolution from atmospheric aerosol deposition to the oceans is important in enhancing and inhibiting phytoplankton growth rates and modifying plankton community structure, thus impacting marine biogeochemistry. Here we review the current state of knowledge on the causes and effects of the leaching of multiple trace metals from natural and anthropogenic aerosols. Aerosol deposition is considered both on short timescales over which phytoplankton respond directly to aerosol metal inputs, as well as longer timescales over which biogeochemical cycles are affected by aerosols.

Pyrogenic iron: the missing link to high iron solubility in aerosols

Abstract: Atmospheric deposition is a source of potentially bioavailable iron (Fe) and thus can partially control biological productivity in large parts of the ocean. However, the explanation of observed high aerosol Fe solubility compared to that in soil particles is still controversial, as several hypotheses have been proposed to explain this observation. Here, a statistical analysis of aerosol Fe solubility estimated from four models and observations compiled from multiple field campaigns suggests that pyrogenic aerosols are the main sources of aerosols with high Fe solubility at low concentration. Additionally, we find that field data over the Southern Ocean display a much wider range in aerosol Fe solubility compared to the models, which indicate an underestimation of labile Fe concentrations by a factor of 15. These findings suggest that pyrogenic Fe-containing aerosols are important sources of atmospheric bioavailable Fe to the open ocean and crucial for predicting anthropogenic perturbations to marine productivity.

Contribution of the world's main dust source regions to the global cycle of desert dust

Abstract: . Even though desert dust is the most abundant aerosol by mass in Earth's atmosphere, the relative contributions of the world's major source regions to the global dust cycle remain poorly constrained. This problem hinders accounting for the potentially large impact of regional differences in dust properties on clouds, the Earth's energy balance, and terrestrial and marine biogeochemical cycles. Here, we constrain the contribution of each of the world's main dust source regions to the global dust cycle. We use an analytical framework that integrates an ensemble of global aerosol model simulations with observationally informed constraints on the dust size distribution, extinction efficiency, and regional dust aerosol optical depth (DAOD). We obtain a dataset that constrains the relative contribution of nine major source regions to size-resolved dust emission, atmospheric loading, DAOD, concentration, and deposition flux. We find that the 22–29 Tg (1 standard error range) global loading of dust with a geometric diameter up to 20 µm is partitioned as follows: North African source regions contribute ∼ 50 % (11–15 Tg), Asian source regions contribute ∼ 40 % (8–13 Tg), and North American and Southern Hemisphere regions contribute ∼ 10 % (1.8–3.2 Tg). These results suggest that current models on average overestimate the contribution of North African sources to atmospheric dust loading at ∼ 65 %, while underestimating the contribution of Asian dust at ∼ 30 %. Our results further show that each source region's dust loading peaks in local spring and summer, which is partially driven by increased dust lifetime in those seasons. We also quantify the dust deposition flux to the Amazon rainforest to be ∼ 10 Tg yr−1, which is a factor of 2–3 less than inferred from satellite data by previous work that likely overestimated dust deposition by underestimating the dust mass extinction efficiency. The data obtained in this paper can be used to obtain improved constraints on dust impacts on clouds, climate, biogeochemical cycles, and other parts of the Earth system.

Occurrence of pristine aerosol environments on a polluted planet

Abstract: Natural aerosols define a preindustrial baseline state from which the magnitude of anthropogenic aerosol effects on climate are calculated and are a major component of the large uncertainty in anthropogenic aerosol−cloud radiative forcing. This uncertainty would be reduced if aerosol environments unperturbed by air pollution could be studied in the present-day atmosphere, but the pervasiveness of air pollution makes identification of unperturbed regions difficult. Here, we use global model simulations to define unperturbed aerosol regions in terms of two measures that compare 1750 and 2000 conditions—the number of days with similar aerosol concentrations and the similarity of the aerosol response to perturbations in model processes and emissions. The analysis shows that the aerosol system in many present-day environments looks and behaves like it did in the preindustrial era. On a global annual mean, unperturbed aerosol regions cover 12% of the Earth (16% of the ocean surface and 2% of the land surface). There is a strong seasonal variation in unperturbed regions of between 4% in August and 27% in January, with the most persistent conditions occurring over the equatorial Pacific. About 90% of unperturbed regions occur in the Southern Hemisphere, but in the Northern Hemisphere, unperturbed conditions are transient and spatially patchy. In cloudy regions with a radiative forcing relative to 1750, model results suggest that unperturbed aerosol conditions could still occur on a small number of days per month. However, these environments are mostly in the Southern Hemisphere, potentially limiting the usefulness in reducing Northern Hemisphere forcing uncertainty.

Glacially sourced dust as a potentially significant source of ice nucleating particles

Abstract: Aeolian dusts serve as ice nucleating particles in mixed-phase clouds, and thereby alter the cloud properties and lifetime. Glacial outwash plains are thought to be a major dust source in cold, high latitudes. Due to the recent rapid and widespread retreat of glaciers, high-latitude dust emissions are projected to increase, especially in the Arctic region, which is highly sensitive to climate change. However, the potential contribution of high-latitude dusts to ice nucleation in Arctic low-level clouds is not well acknowledged. Here we show that glacial outwash sediments in Svalbard (a proxy for glacially sourced dusts) have a remarkably high ice nucleating ability under conditions relevant for mixed-phase cloud formation, as compared with typical mineral dusts. The high ice nucleating ability of the sediments is probably governed by the presence of small amounts of organic matter (<1 wt% organic carbon) rather than mineral components. In addition, our results from intensive field measurements and model simulations indicate that the concentrations of atmospheric ice nucleating particles over the Svalbard region are expected to be enhanced in the summertime under the influence of dust emissions from Svalbard and its surroundings. We suggest that high-latitude dust sources have the potential to significantly influence glaciation of Arctic low-level clouds. Dusts from glaciers may contribute significantly to ice nucleation in Arctic low-level clouds, according to analyses of glacial outwash sediments in Svalbard.

More Evidence Linking Arctic Amplification to Extreme Weather in Mid-Latitudes

Abstract: [1] Arctic amplification (AA) – the observed enhanced warming in high northern latitudes relative to the northern hemisphere – is evident in lower-tropospheric temperatures and in 1000-to-500 hPa thicknesses. Daily fields of 500 hPa heights from the National Centers for Environmental Prediction Reanalysis are analyzed over N. America and the N. Atlantic to assess changes in north-south (Rossby) wave characteristics associated with AA and the relaxation of poleward thickness gradients. Two effects are identified that each contribute to a slower eastward progression of Rossby waves in the upper-level flow: 1) weakened zonal winds, and 2) increased wave amplitude. These effects are particularly evident in autumn and winter consistent with sea-ice loss, but are also apparent in summer, possibly related to earlier snow melt on high-latitude land. Slower progression of upper-level waves would cause associated weather patterns in mid-latitudes to be more persistent, which may lead to an increased probability of extreme weather events that result from prolonged conditions, such as drought, flooding, cold spells, and heat waves.

Anthropogenic aerosols and the weakening of the South Asian summer monsoon

Abstract: Changes in monsoon rainfall are caused by human-produced aerosols slowing the tropical atmospheric circulation. Observations show that South Asia underwent a widespread summertime drying during the second half of the 20th century, but it is unclear whether this trend was due to natural variations or human activities. We used a series of climate model experiments to investigate the South Asian monsoon response to natural and anthropogenic forcings. We find that the observed precipitation decrease can be attributed mainly to human-influenced aerosol emissions. The drying is a robust outcome of a slowdown of the tropical meridional overturning circulation, which compensates for the aerosol-induced energy imbalance between the Northern and Southern Hemispheres. These results provide compelling evidence of the prominent role of aerosols in shaping regional climate change over South Asia.

Improving our fundamental understanding of the role of aerosol−cloud interactions in the climate system

Abstract: The effect of an increase in atmospheric aerosol concentrations on the distribution and radiative properties of Earth’s clouds is the most uncertain component of the overall global radiative forcing from preindustrial time. General circulation models (GCMs) are the tool for predicting future climate, but the treatment of aerosols, clouds, and aerosol−cloud radiative effects carries large uncertainties that directly affect GCM predictions, such as climate sensitivity. Predictions are hampered by the large range of scales of interaction between various components that need to be captured. Observation systems (remote sensing, in situ) are increasingly being used to constrain predictions, but significant challenges exist, to some extent because of the large range of scales and the fact that the various measuring systems tend to address different scales. Fine-scale models represent clouds, aerosols, and aerosol−cloud interactions with high fidelity but do not include interactions with the larger scale and are therefore limited from a climatic point of view. We suggest strategies for improving estimates of aerosol−cloud relationships in climate models, for new remote sensing and in situ measurements, and for quantifying and reducing model uncertainty.

Evaluation of CMIP6 DECK Experiments With CNRM-CM6-1

Abstract: This paper describes the main characteristics of CNRM-CM6-1, the fully coupled atmosphere-ocean general circulation model of sixth generation jointly developed by Centre National de Recherches Meteorologiques (CNRM) and Cerfacs for the sixth phase of the Coupled Model Intercomparison Project 6 (CMIP6). The paper provides a description of each component of CNRM-CM6-1, including the coupling method and the new online output software. We emphasize where model's components have been updated with respect to the former model version, CNRM-CM5.1. In particular, we highlight major improvements in the representation of atmospheric and land processes. A particular attention has also been devoted to mass and energy conservation in the simulated climate system to limit long-term drifts. The climate simulated by CNRM-CM6-1 is then evaluated using CMIP6 historical and Diagnostic, Evaluation and Characterization of Klima (DECK) experiments in comparison with CMIP5 CNRM-CM5.1 equivalent experiments. Overall, the mean surface biases are of similar magnitude but with different spatial patterns. Deep ocean biases are generally reduced, whereas sea ice is too thin in the Arctic. Although the simulated climate variability remains roughly consistent with CNRM-CM5.1, its sensitivity to rising CO 2 has increased: the equilibrium climate sensitivity is 4.9 K, which is now close to the upper bound of the range estimated from CMIP5 models.