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Abstract Several cloud retrieval algorithms based on satellite observations in the infrared have been developed in the last decades. However, these observations only cover the midinfrared (MIR, λ < 15 μm) part of the spectrum, and none are available in the far‐infrared (FIR, λ ≥ 15 μm). Using the optimal estimation method, we show that adding a few FIR channels to existing spaceborne radiometers would significantly improve their ability to retrieve ice cloud radiative properties. For clouds encountered in the polar regions and the upper troposphere, where the atmosphere is sufficiently transparent in the FIR, using FIR channels would reduce by more than 50% the uncertainties on retrieved values of optical thickness, effective particle diameter, and cloud top altitude. Notably, this would extend the range of applicability of current retrieval methods to the polar regions and to clouds with large optical thickness, where MIR algorithms perform poorly. The high performance of solar reflection‐based algorithms would thus be reached in nighttime conditions. Since the sensitivity of ice cloud thermal emission to effective particle diameter is approximately 5 times larger in the FIR than in the MIR, using FIR observations is a promising venue for studying ice cloud microphysics and precipitation processes. This is highly relevant for cirrus clouds and convective towers. This is also essential to study precipitation in the driest regions of the atmosphere, where strong feedbacks are at play between clouds and water vapor. The deployment in the near future of a FIR spaceborne radiometer is technologically feasible and should be strongly supported. , Plain Language Summary The size of ice cloud particles can be estimated from space by measuring the infrared emission of ice clouds. However, this method no longer works when clouds are too thick or when particles are too large, although such clouds are encountered in many regions of the Earth and are critical for the Earth's climate. Using new sensors that measure cloud emission at longer wavelengths, in the so‐called far‐infrared region, would extend the potential of satellite observations to thick clouds, to clouds made of larger particles, and to clouds found in the polar regions which are very poorly known. These new sensors have become available in the last years, but none is deployed in space so far. We show that a satellite equipped with a few channels in the far‐infrared would greatly increase our capacity to observe ice clouds. This is promising for our understanding of cloud microphysics and precipitation in general, and for studying the water cycle in the polar regions in particular. For these reasons, it is highly recommended to deploy a far‐infrared radiometer in space. , Key Points Ice cloud remote sensing would be greatly improved by adding far‐infrared channels to existing midinfrared spaceborne radiometers Far‐infrared radiometry is well suited to study ice clouds in the polar regions and upper troposphere Using far‐infrared radiometry extends current infrared capabilities to large optical thickness and large cloud particles

The hypothesis according to which higher sulphate concentrations favor ice clouds made of larger ice crystals is tested using data sets from the CloudSat and Cloud‐Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) satellites. This is a potential consequence of the sulphate‐induced freezing inhibition (SIFI) effect, namely, the hypothesis that sulphates contribute to inhibit the onset of ice crystal formation by deactivating ice‐forming nuclei during Arctic winter. A simple index based on the backscattering at 532 nm and the color ratio from the CALIPSO lidar measurements is compared against in situ sulphate concentration time series and used as a proxy for this variable. An algorithm using the lidar data and the CloudSat radar microphysical retrievals is also developed for identifying cloud types, focusing on those supposedly favored by the SIFI effect. The analysis includes the effect of the lidar off‐nadir angle on the sulphate index and the cloud classification, the validation of the index, as well as the production of circum‐Arctic maps of the sulphate index and of the SIFI‐favored clouds fraction. The increase of the lidar off‐nadir angle is shown to cause an increase in the measured depolarization ratio and hence in the ability to detect ice crystals. The index correlates positively with both sulphates and sea salt concentrations, with a Pearson correlation coefficient ( ) varying from 0.10 to 0.42 for the different comparisons performed. Ultimate findings are the results of two correlation tests of the SIFI effect, which allow for a new outlook on its possible role in the Arctic troposphere during winter.

Abstract Several far‐infrared (FIR) satellite missions are planned for the next decade, with a special interest for the Arctic region. A theoretical study is performed to help with the design of an FIR radiometer, whose configuration in terms of channels number and frequencies is optimized based on information content analysis. The problem is cast in a context of vertical column experiments (1D) to determine the optimal configuration of a FIR radiometer to study the Arctic polar night. If only observations of the FIR radiometer were assimilated, the results show that for humidity, 90% of the total information content is obtained with four bands, whereas for temperature, 10 bands are needed. When the FIR measurements are assimilated on top of those from the advanced infrared sounder (AIRS), the former bring in additional information between the surface and 850 hPa and from 550 to 250 hPa for humidity. Moreover, between 400 and 200 hPa, the FIR radiometer is better than AIRS at reducing the analysis error variance for humidity. This indicates the potential of FIR observations for improving water vapor analysis in the Arctic. , Key Points FIR channels add information for UTLS water vapor compared to standard MIR channels IC is used to optimize the channels frequencies and widths of a FIR radiometer A high DFS is reached with only a few channels of an optimized FIR radiometer

Data sets from CloudSat radar reflectivity and CALIPSO lidar backscattering measurements provide a new regard on Arctic and Antarctic winter cloud systems, as well as on the way aerosols determine their formation and evolution. Especially, links between the cloud ice crystal size and the surrounding aerosol field may be further investigated. In this study, the satellite observations are used to heuristically separate polar thin ice clouds into two crystal size categories, and an aerosol index based on the attenuated backscattering and color ratio of the sampled volumes is used for identifying haze in cloud‐free regions. Statistics from 386 Arctic satellite overpasses during January 2007 and from 379 overpasses over Antarctica during July 2007 reveal that sectors with the highest proportion of thin ice clouds having large ice crystals at their top are those for which the aerosol index is highest. Moreover, a weak but significant correlation between the cloud top ice effective radius and the above‐cloud aerosol index suggests that more polluted clouds tend to have higher ice effective radius, in 10 of the 11 sectors investigated. These results are interpreted in terms of a sulphate‐induced freezing inhibition effect.

Polar clouds are, as a consequence of the paucity of in situ observations, poorly understood compared to their lower latitude analogs, yet highly climate-sensitive through thermal radiation emission. The prevalence of Thin Ice Clouds (TIC) dominates in cold Polar Regions and the Upper Troposphere Lower Stratosphere (UTLS) altitudes. They can be grouped into 2 broad categories. The first thin ice cloud type (TIC1) is made up of high concentrations of small, non-precipitating ice crystals. The second type (TIC2) is composed of relatively small concentrations of larger, precipitating ice crystals. In this study, we investigate the ability of a developmental version of the Canadian Regional Climate Model (CRCM6) in simulating cold polar-night clouds over the Arctic Ocean, a remote region that is critical to atmospheric circulation reaching out to the mid-latitudes. The results show that, relative to CloudSat-CALIPSO vertical profile products, CRCM6 simulates high-latitude and low spatial frequency variations of Ice Water Content (IWC), effective radius (re) and cooling rates reasonably well with only small to moderate wet and dry biases. The model can also simulate cloud type, location, and temporal occurrence effectively. As well, it successfully simulated higher altitude TIC1 clouds whose small size evaded CloudSat detection while being visible to CALIPSO.

Two Types of Ice Clouds (TICs) have been characterized in the Arctic during the polar night and early spring. TIC-1 are composed by non-precipitating small ice crystals of less than 30 µm in diameter. The second type, TIC-2, are characterized by a low concentration of large precipitating ice crystals (>30 µm). Here, we evaluate the Weather Research and Forecasting (WRF) model performance both in space and time after implementing a parameterization based on a stochastic approach dedicated to the simulation of ice clouds in the Arctic. Well documented reference cases provided us in situ data from the spring of 2008 Indirect and Semi-Direct Aerosol Campaign (ISDAC) campaign over Alaska. Simulations of the microphysical properties of the TIC-2 clouds on 15 and 25 April 2008 (polluted or acidic cases) and TIC-1 clouds on non-polluted cases are compared to DARDAR (raDAR/liDAR) satellite products. Our results show that the stochastic approach based on the classical nucleation theory, with the appropriate contact angle, is better than the original scheme in WRF model to represent TIC-1 and TIC-2 properties (ice crystal concentration and size) in response to the IN acidification.

Abstract. Starphotometry, the night-time counterpart of sunphotometry, has not yet achieved the commonly sought observational error level of 1 %: a spectral optical depth (OD) error level of 0.01. In order to address this issue, we investigate a large variety of systematic (absolute) uncertainty sources. The bright-star catalogue of extraterrestrial references is noted as a major source of errors with an attendant recommendation that its accuracy, particularly its spectral photometric variability, be significantly improved. The small field of view (FOV) employed in starphotometry ensures that it, unlike sun- or moonphotometry, is only weakly dependent on the intrinsic and artificial OD reduction induced by scattering into the FOV by optically thin clouds. A FOV of 45 arcsec (arcseconds) was found to be the best trade-off for minimizing such forward-scattering errors concurrently with flux loss through vignetting. The importance of monitoring the sky background and using interpolation techniques to avoid spikes and to compensate for measurement delay was underscored. A set of 20 channels was identified to mitigate contamination errors associated with stellar and terrestrial atmospheric gas absorptions, as well as aurora and airglow emissions. We also note that observations made with starphotometers similar to our High Arctic instrument should be made at high angular elevations (i.e. at air masses less than 5). We noted the significant effects of snow crystal deposition on the starphotometer optics, how pseudo OD increases associated with this type of contamination could be detected, and how proactive techniques could be employed to avoid their occurrence in the first place. If all of these recommendations are followed, one may aspire to achieve component errors that are well below 0.01: in the process, one may attain a total 0.01 OD target error.

Abstract. In the Arctic, during polar night and early spring, ice clouds are separated into two leading types of ice clouds (TICs): (1) TIC1 clouds characterized by a large concentration of very small crystals and TIC2 clouds characterized by a low concentration of large ice crystals. Using a suitable parameterization of heterogeneous ice nucleation is essential for properly representing ice clouds in meteorological and climate models and subsequently understanding their interactions with aerosols and radiation. Here, we describe a new parameterization for ice crystal formation by heterogeneous nucleation in water-subsaturated conditions coupled to aerosol chemistry in the Weather Research and Forecasting model coupled with chemistry (WRF-Chem). The parameterization is implemented in the Milbrandt and Yau (2005a, b) two-moment cloud microphysics scheme, and we assess how the WRF-Chem model responds to the run-time interaction between chemistry and the new parameterization. Well-documented reference cases provided us with in situ data from the spring 2008 Indirect and Semi-Direct Aerosol Campaign (ISDAC) over Alaska. Our analysis reveals that the new parameterization clearly improves the representation of the ice water content (IWC) in polluted or unpolluted air masses and shows the poor performance of the reference parameterization in representing ice clouds with low IWC. The new parameterization is able to represent TIC1 and TIC2 microphysical characteristics at the top of the clouds, where heterogenous ice nucleation is most likely occurring, even with the known bias of simulated aerosols by WRF-Chem over the Arctic.

Aerosol–cloud interactions present a large source of uncertainties in atmospheric and climate models. One of the main challenges to simulate ice clouds is to reproduce the right ice nucleating particle concentration. In this study, we derive a parameterization for immersion freezing according to the classical nucleation theory. Our objective was to constrain this parameterization with observations taken over the Canadian Arctic during the Amundsen summer 2014 and 2016 campaigns. We found a linear dependence of contact angle and temperature. Using this approach, we were able to reproduce the scatter in ice nucleated particle concentrations within a factor 5 of observed values with a small negative bias. This parameterization would be easy to implement in climate and atmospheric models, but its representativeness has to first be validated against other datasets.

Abstract The increasing atmospheric nitrous oxide (N 2 O) concentration stems from the development of agriculture. However, N 2 O emissions from global rice‐based ecosystems have not been explicitly and systematically quantified. Therefore, this study aims to estimate the spatiotemporal magnitudes of the N 2 O emissions from global rice‐based ecosystems and determine different contribution factors by improving a process‐based biogeochemical model, TRIPLEX‐GHG v2.0. Model validation suggested that the modeled N 2 O agreed well with field observations under varying management practices at daily, seasonal, and annual steps. Simulated N 2 O emissions from global rice‐based ecosystems exhibited significant increasing trends from 0.026 ± 0.0013 to 0.18 ± 0.003 TgN yr −1 from 1910 to 2020, with ∼69.5% emissions attributed to the rice‐growing seasons. Irrigated rice ecosystems accounted for a majority of global rice N 2 O emissions (∼76.9%) because of their higher N 2 O emission rates than rainfed systems. Regarding spatial analysis, Southern China, Northeast India, and Southeast Asia are hotspots for rice‐based N 2 O emissions. Experimental scenarios revealed that N fertilizer is the largest global rice‐N 2 O source, especially since the 1960s (0.047 ± 0.010 TgN yr −1 , 35.24%), while the impact of expanded irrigation plays a minor role. Overall, this study provides a better understanding of the rice‐based ecosystem in the global agricultural N 2 O budget; further, it quantitively demonstrated the central role of N fertilizer in rice‐based N 2 O emissions by including rice crop calendars, covering non‐rice growing seasons, and differentiating the effects of various water regimes and input N forms. Our findings emphasize the significance of co‐management of N fertilizer and water regimes in reducing the net climate impact of global rice cultivation. , Plain Language Summary Nitrous oxide (N 2 O) is a greenhouse gas with ∼300 times greater effect on climate warming than carbon dioxide. Global croplands represent the largest source of anthropogenic N 2 O emissions. However, the contribution of global rice‐based cropping ecosystems to the N 2 O budget remains largely uncertain because of inconsistent observed results. Inspired by the increasing availability of reliable global data sets, we improved and applied a process‐based biogeochemical model by describing the dynamics of various microbial activities to simulate N 2 O emissions from rice‐based ecosystems on a global scale. Model simulations showed that 0.18 million tons of N 2 O‐N were emitted from global rice‐based N 2 O emissions in the 2010s, which was five times larger than that in the 1910s. In the context of regional contribution, southern China, northern India, and Southeast Asia are responsible for more than 80% of the total emissions during 1910–2020. Results suggest that N fertilizer is the most important rice‐N 2 O source quantitively and that increasing irrigation exerts a buffering effect. This study confirmed the potential mitigating effect of co‐managing N fertilizer and irrigation on mitigating rice‐based N 2 O emissions globally. , Key Points N 2 O emissions from global rice‐based ecosystem increased from 0.026 to 0.18 TgN yr −1 between 1910 and 2020 Irrigated rice‐based ecosystems showed larger N 2 O fluxes than rainfed rice globally due to higher N fertilizer use and frequent aerations N fertilizer represents the largest N 2 O source, and co‐management of N fertilizer and flooding regimes is important for mitigation

Abstract. The changing Arctic climate is creating increased economic, transportation, and recreational activities requiring reliable and relevant weather information. However, the Canadian Arctic is sparsely observed, and processes governing weather systems in the Arctic are not well understood. There is a recognized lack of meteorological data to characterize the Arctic atmosphere for operational forecasting and to support process studies, satellite calibration/validation, search and rescue operations (which are increasing in the region), high-impact weather (HIW) detection and prediction, and numerical weather prediction (NWP) model verification and evaluation. To address this need, Environment and Climate Change Canada commissioned two supersites, one in Iqaluit (63.74∘ N, 68.51∘ W) in September 2015 and the other in Whitehorse (60.71∘ N, 135.07∘ W) in November 2017 as part of the Canadian Arctic Weather Science (CAWS) project. The primary goals of CAWS are to provide enhanced meteorological observations in the Canadian Arctic for HIW nowcasting (short-range forecast) and NWP model verification, evaluation, and process studies and to provide recommendations on the optimal cost-effective observing system for the Canadian Arctic. Both sites are in provincial/territorial capitals and are economic hubs for the region; they also act as transportation gateways to the north and are in the path of several common Arctic storm tracks. The supersites are located at or next to major airports and existing Meteorological Service of Canada ground-based weather stations that provide standard meteorological surface observations and upper-air radiosonde observations; they are also uniquely situated in close proximity to frequent overpasses by polar-orbiting satellites. The suite of in situ and remote sensing instruments at each site is completely automated (no on-site operator) and operates continuously in all weather conditions, providing near-real-time data to operational weather forecasters, the public, and researchers via obrs.ca. The two sites have similar instruments, including mobile Doppler weather radars, multiple vertically profiling and/or scanning lidars (Doppler, ceilometer, water vapour), optical disdrometers, precipitation gauges in different shielded configurations, present weather sensors, fog monitoring devices, radiation flux sensors, and other meteorological instruments. Details on the two supersites, the suites of instruments deployed, the data collection methods, and example case studies of HIW events are discussed. CAWS data are publicly accessible via the Canadian Government Open Data Portal (https://doi.org/10.18164/ff771396-b22c-4bc3-844d-38fc697049e9, Mariani et al., 2022a, and https://doi.org/10.18164/d92ed3cf-4ba0-4473-beec-357ec45b0e78, Mariani et al., 2022b); this dataset is being used to improve our understanding of synoptic and fine-scale meteorological processes in the Arctic and sub-Arctic, including HIW detection and prediction and NWP verification, assimilation, and processes.

Abstract. A far infrared radiometer (FIRR) dedicated to measuring radiation emitted by clear and cloudy atmospheres was developed in the framework of the Thin Ice Clouds in Far InfraRed Experiment (TICFIRE) technology demonstration satellite project. The FIRR detector is an array of 80 × 60 uncooled microbolometers coated with gold black to enhance the absorptivity and responsivity. A filter wheel is used to select atmospheric radiation in nine spectral bands ranging from 8 to 50 µm. Calibrated radiances are obtained using two well-calibrated blackbodies. Images are acquired at a frame rate of 120 Hz, and temporally averaged to reduce electronic noise. A complete measurement sequence takes about 120 s. With a field of view of 6°, the FIRR is not intended to be an imager. Hence spatial average is computed over 193 illuminated pixels to increase the signal-to-noise ratio and consequently the detector resolution. This results in an improvement by a factor of 5 compared to individual pixel measurements. Another threefold increase in resolution is obtained using 193 non-illuminated pixels to remove correlated electronic noise, leading an overall resolution of approximately 0.015 W m−2 sr−1. Laboratory measurements performed on well-known targets suggest an absolute accuracy close to 0.02 W m−2 sr−1, which ensures atmospheric radiance is retrieved with an accuracy better than 1 %. Preliminary in situ experiments performed from the ground in winter and in summer on clear and cloudy atmospheres are compared to radiative transfer simulations. They point out the FIRR ability to detect clouds and changes in relative humidity of a few percent in various atmospheric conditions, paving the way for the development of new algorithms dedicated to ice cloud characterization and water vapor retrieval.

Abstract. The first airborne measurements of the Far-InfraRed Radiometer (FIRR) were performed in April 2015 during the panarctic NETCARE campaign. Vertical profiles of spectral upwelling radiance in the range 8–50 µm were measured in clear and cloudy conditions from the surface up to 6 km. The clear sky profiles highlight the strong dependence of radiative fluxes to the temperature inversion typical of the Arctic. Measurements acquired for total column water vapour from 1.5 to 10.5 mm also underline the sensitivity of the far-infrared greenhouse effect to specific humidity. The cloudy cases show that optically thin ice clouds increase the cooling rate of the atmosphere, making them important pieces of the Arctic energy balance. One such cloud exhibited a very complex spatial structure, characterized by large horizontal heterogeneities at the kilometre scale. This emphasizes the difficulty of obtaining representative cloud observations with airborne measurements but also points out how challenging it is to model polar clouds radiative effects. These radiance measurements were successfully compared to simulations, suggesting that state-of-the-art radiative transfer models are suited to study the cold and dry Arctic atmosphere. Although FIRR in situ performances compare well to its laboratory performances, complementary simulations show that upgrading the FIRR radiometric resolution would greatly increase its sensitivity to atmospheric and cloud properties. Improved instrument temperature stability in flight and expected technological progress should help meet this objective. The campaign overall highlights the potential for airborne far-infrared radiometry and constitutes a relevant reference for future similar studies dedicated to the Arctic and for the development of spaceborne instruments.

Abstract. Motivated by the need to predict how the Arctic atmosphere will change in a warming world, this article summarizes recent advances made by the research consortium NETCARE (Network on Climate and Aerosols: Addressing Key Uncertainties in Remote Canadian Environments) that contribute to our fundamental understanding of Arctic aerosol particles as they relate to climate forcing. The overall goal of NETCARE research has been to use an interdisciplinary approach encompassing extensive field observations and a range of chemical transport, earth system, and biogeochemical models. Several major findings and advances have emerged from NETCARE since its formation in 2013. (1) Unexpectedly high summertime dimethyl sulfide (DMS) levels were identified in ocean water (up to 75 nM) and the overlying atmosphere (up to 1 ppbv) in the Canadian Arctic Archipelago (CAA). Furthermore, melt ponds, which are widely prevalent, were identified as an important DMS source (with DMS concentrations of up to 6 nM and a potential contribution to atmospheric DMS of 20 % in the study area). (2) Evidence of widespread particle nucleation and growth in the marine boundary layer was found in the CAA in the summertime, with these events observed on 41 % of days in a 2016 cruise. As well, at Alert, Nunavut, particles that are newly formed and grown under conditions of minimal anthropogenic influence during the months of July and August are estimated to contribute 20 % to 80 % of the 30–50 nm particle number density. DMS-oxidation-driven nucleation is facilitated by the presence of atmospheric ammonia arising from seabird-colony emissions, and potentially also from coastal regions, tundra, and biomass burning. Via accumulation of secondary organic aerosol (SOA), a significant fraction of the new particles grow to sizes that are active in cloud droplet formation. Although the gaseous precursors to Arctic marine SOA remain poorly defined, the measured levels of common continental SOA precursors (isoprene and monoterpenes) were low, whereas elevated mixing ratios of oxygenated volatile organic compounds (OVOCs) were inferred to arise via processes involving the sea surface microlayer. (3) The variability in the vertical distribution of black carbon (BC) under both springtime Arctic haze and more pristine summertime aerosol conditions was observed. Measured particle size distributions and mixing states were used to constrain, for the first time, calculations of aerosol–climate interactions under Arctic conditions. Aircraft- and ground-based measurements were used to better establish the BC source regions that supply the Arctic via long-range transport mechanisms, with evidence for a dominant springtime contribution from eastern and southern Asia to the middle troposphere, and a major contribution from northern Asia to the surface. (4) Measurements of ice nucleating particles (INPs) in the Arctic indicate that a major source of these particles is mineral dust, likely derived from local sources in the summer and long-range transport in the spring. In addition, INPs are abundant in the sea surface microlayer in the Arctic, and possibly play a role in ice nucleation in the atmosphere when mineral dust concentrations are low. (5) Amongst multiple aerosol components, BC was observed to have the smallest effective deposition velocities to high Arctic snow (0.03 cm s−1).