Earth Systems

In recent years Southeast Asia has seen a significant increase in the intensity and frequency of haze events, or days in which visibility falls below 10 kilometers. Caused by airborne particulates known as aerosols, such low-visibility days reduce air quality and endanger human health. The main sources of the pollution are human activities that produce fires—biomass burning chief among them—and those that do not, such as fossil fuel combustion, construction and road dust.

A coordinated set of Arctic modelling experiments, which explore how the Arctic responds to changes in external forcing, is proposed. Our goal is to compute and compare climate response functions (CRFs) – the transient response of key observable indicators such as sea-ice extent, freshwater content of the Beaufort Gyre, etc. – to abrupt step changes in forcing fields across a number of Arctic models. Changes in wind, freshwater sources, and inflows to the Arctic basin are considered. Convolutions of known or postulated time series of these forcing fields with their respective CRFs then yield the (linear) response of these observables. This allows the project to inform, and interface directly with, Arctic observations and observers and the climate change community. Here we outline the rationale behind such experiments and illustrate our approach in the context of a coarse-resolution model of the Arctic based on the MITgcm. We conclude by summarizing the expected benefits of such an activity and encourage other modelling groups to compute CRFs with their own models so that we might begin to document their robustness to model formulation, resolution, and parameterization.

Atmospheric greenhouse gas (GHG) concentrations are at unprecedented, record-high levels compared to the last 800 000 years. Those elevated GHG concentrations warm the planet and – partially offset by net cooling effects by aerosols – are largely responsible for the observed warming over the past 150 years. An accurate representation of GHG concentrations is hence important to understand and model recent climate change. So far, community efforts to create composite datasets of GHG concentrations with seasonal and latitudinal information have focused on marine boundary layer conditions and recent trends since the 1980s. Here, we provide consolidated datasets of historical atmospheric concentrations (mole fractions) of 43 GHGs to be used in the Climate Model Intercomparison Project – Phase 6 (CMIP6) experiments. The presented datasets are based on AGAGE and NOAA networks, firn and ice core data, and archived air data, and a large set of published studies. In contrast to previous intercomparisons, the new datasets are latitudinally resolved and include seasonality. We focus on the period 1850–2014 for historical CMIP6 runs, but data are also provided for the last 2000 years. We provide consolidated datasets in various spatiotemporal resolutions for carbon dioxide (CO2), methane (CH4) and nitrous oxide (N2O), as well as 40 other GHGs, namely 17 ozone-depleting substances, 11 hydrofluorocarbons (HFCs), 9 perfluorocarbons (PFCs), sulfur hexafluoride (SF6), nitrogen trifluoride (NF3) and sulfuryl fluoride (SO2F2). In addition, we provide three equivalence species that aggregate concentrations of GHGs other than CO2, CH4 and N2O, weighted by their radiative forcing efficiencies. For the year 1850, which is used for pre-industrial control runs, we estimate annual global-mean surface concentrations of CO2 at 284.3 ppm, CH4 at 808.2 ppb and N2O at 273.0 ppb. The data are available at https://esgf-node.llnl.gov/search/input4mips/ and http://www.climatecollege.unimelb.edu.au/cmip6. While the minimum CMIP6 recommendation is to use the global- and annual-mean time series, modelling groups can also choose our monthly and latitudinally resolved concentrations, which imply a stronger radiative forcing in the Northern Hemisphere winter (due to the latitudinal gradient and seasonality).

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