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The optical properties of the laboratory tholin is considered, and an attempt is made to critically evaluate the analog between laboratory tholin and Titan tholin. The processes that form the solid haze material from the gaseous atmosphere are considered. It is suggested that the N/C ratio may be a useful signature of the processes that determine the haze production rate.
An analysis is conducted of spatially resolved Voyager 2 Photopolarimeter Subsystem (PPS) observations at 2650 and 7500 A. The continuum absorber that is tropospherically abundant, if confined to the region below the methane haze layer, indicates an optical depth for that layer no greater than 0.8; models in which this optical depth is as large as 3.0 yield too much limb darkening, in the case where the continuum absorber is mixed with both the methane haze and deeper clouds. Tropospheric aerosols are noted to have phase functions with shallow backward lobes.
The effect of carbonaceous Arctic haze on the surface energy balance was investigated using a specially developed one-dimensional three-component numerical model which accounts for the transfer of IR and solar radiation through the atmosphere, turbulent mixing within the boundary layer, and heat conduction through snow-capped sea ice. The results of calculations indicate that, when haze is present, the surface temperature increases, provided the relative humidity through the column does not change. The increase is due to an increase in the absorbed radiation at the surface.
An international cooperative project between the National Aeronautics and Space Administration (NASA) and the European Space Agency (ESA) is planning to send a probe into the atmosphere of Titan (a moon of Saturn) as part of the Cassini Mission to Saturn. This paper analyzes the feasibility of measuring the intensity of atomic carbon and hydrogen line emission in the shock layer during the high velocity portion of the entry to determine the number density and composition of the organic haze particles in the Titan atmosphere. Analysis indicates that the line radiation signal-to-noise ratios are high enough so that determination of the haze particle number density and composition appears to be feasible. The analysis may be applicable to other future planetary missions.
Earth's atmospheric composition at the time of the origin of life is not known, but it has often been suggested that chemical transformation of reactive species in the atmosphere was a significant source of pre biotic organic molecules. Experimental and theoretical studies over the past half century have shown that atmospheric synthesis can yield molecules such as amino acids and nucleobases, but these processes are very sensitive to gas composition and energy source. Abiotic synthesis of organic molecules is more productive in reduced atmospheres, yet the primitive Earth may not have been as reducing as earlier workers assumed, and recent research has reflected this shift in thinking. This work provides a survey of the range of chemical products that can be produced given a set of atmospheric conditions, with a particular focus on recent reports. Intertwined with the discussion of atmospheric synthesis is the consideration of an organic haze layer, which has been suggested as a possible ultraviolet shield on the anoxic early Earth. Since such a haze layer - if formed - would serve as a reservoir for organic molecules, the chemical composition of the aerosol should be closely examined. The results highlighted here show that a variety of products can be formed in mildly reducing or even neutral atmospheres, demonstrating that contributions of atmospheric synthesis to the organic inventory on early Earth should not be discounted. This review intends to bridge current knowledge of the range of possible atmospheric conditions in the prebiotic environment and pathways for synthesis under such conditions by examining the possible products of organic chemistry in the early atmosphere.
The first young giant planet to be discovered by the Gemini Planet Imager was the (is) approximately 2MJ planet 51 Eri b. This approximately 20 Myr old young Jupiter is the first directly imaged planet to show unmistakable methane in H band. To constrain the planet's mass, atmospheric temperature, and composition, the GPI J and H band spectra as well as some limited photometric points were compared to the predictions of substellar atmosphere models. The best fitting models reported in the discovery paper (Macintosh et al. 2015) relied upon a combination of clear and cloudy atmospheric columns to reproduce the data. However for an object as cool as 700 K, the origin of the cloud coverage is somewhat puzzling, as the global silicate and iron clouds would be expected to have sunk well below the photosphere by this effective temperature. While strong vertical mixing in these low gravity atmospheres remains a plausible explanation, we have explored whether atmospheric photochemistry, driven by the UV flux from the primary star, may yield hazes that also influence the observed spectrum of the planet. To explore this possibility we have modeled the atmospheric photochemistry of 51 Eri b using two state-of-the-art photochemical models, both capable of predicting yields of complex hydrocarbons under various atmospheric conditions. In our presentation we will summarize the modeling approach employed to characterize 51 Eri b, explaining constraints on the planet's effective temperature, gravity, and atmospheric composition and also present results of our studies of atmospheric photochemistry. We will discuss whether photochemical hazes could indeed be responsible for the particulate opacity that apparently sculpts the spectrum of the planet.
The TRAPPIST-1 system, consisting of an ultracool host star having seven known Earth-sized planets, will be a prime target for atmospheric characterization with the James Webb Space Telescope (JWST). However, the detectability of atmospheric molecular species may be severely impacted by the presence of clouds and/or hazes. In this work, we perform 3D general circulation model (GCM) simulations with the LMD-G model supplemented by 1D photochemistry simulations at the terminator with the Atmos model to simulate several possible atmospheres for TRAPPIST-1e, 1f, and 1g: (1) modern Earth, (2) Archean Earth, and (3) CO2-rich atmospheres. The JWST synthetic transit spectra were computed using the GSFC Planetary Spectrum Generator. We find that the TRAPPIST-1e, 1f, and 1g atmospheres, with clouds and/or hazes, could be detected using JWST's NIRSpec Prism from the CO2 absorption line at 4.3 μm in less than 15 transits at 3σ or less than 35 transits at 5σ. However, our analysis suggests that other gases would require hundreds (or thousands) of transits to be detectable. We also find that H2O, mostly confined in the lower atmosphere, is very challenging to detect for these planets or similar systems if the planets' atmospheres are not in a moist greenhouse state. This result demonstrates that the use of GCMs, self-consistently taking into account the effect of clouds and subsaturation, is crucial to evaluate the detectability of atmospheric molecules of interest, as well as for interpreting future detections in a more global (and thus robust and relevant) approach.
The chemistry of trace sulfur gases in planetary organic haze formation is poorly understood, though both are ubiquitous in planetary atmospheres. Here, we perform laboratory studies to explore how the addition of trace amounts of H2S (0.5–5 ppmv) affects organic aerosol produced from ultraviolet photochemistry of CH4 in N2. We analyze the aerosol product composition and size in real time. Inclusion of trace amounts of H2S in the precursor mixture significantly enhances the formation of organic aerosol mass and the particle effective density, both of which increase as a function of initial H2S concentration and in the absence of an additional carbon source. We further present evidence that the addition of trace H2S to the precursor mixtures leads to the formation of organosulfur compounds. Their inclusion in the aerosol-phase contributes to the organic aerosol mass enhancement. Thiyl-alkene chemistry is proposed as a possible organosulfur formation mechanism. In contrast to previous assumptions that sulfur and carbon chemistry occur largely independently of each other, these results suggest a coupling between the two chemistries. This coupling has potential impacts on organic haze and atmospheric sulfur chemistry in planetary atmospheres.
The 'blue haze' is an absorbing smoke, dark as soot in reflection, red in transmission. Its currently accepted explanation by pure scattering (omnidirectional or forward) is untenable, as it would either increase the surface brightness of fall to obscure the surface details. The limb darkening of Mars is mainly the results of absorption by the smoke. The opacity of the Martian atmosphere increases from the red toward the violet. The extinction by the Martian atmosphere is greater than that by the terrestrial at all wavelengths, but only about 20 per cent of the Martian extinction is due to scattering. Dollfus' polarimeteric estimate, corrected for self-absorption, corresponds to a martian atmospheric pressure of 87 mm Hg. The photochemical breakup of carbon dioxide and the escape of oxygen must lead to considerable concentrations of carbon monoxide in the martian atmosphere.
Martian blue haze properties correlated with interplanetary dust, meteor showers and solar flares
Radiance and polarization of multiple scattered light from haze and clouds calculated from Stokes vectors by Monte Carlo method
Most of our existing knowledge of cloud chemistry in regards to forming secondary organic aerosols (SOA) is based on measurements in bulk aqueous solutions. However, SOA reaction kinetics derived from bulk solution measurements might differ from the kinetics in actual cloud droplets, since turbulent mixing and ionic strengths, and ratio of surface area to volume in individual cloud droplets might vary substantially from bulk solutions in the real atmosphere. Three-dimensional models at various scales have been used to simulate aqueous chemistry. However, most of these models do not resolve turbulence down to the smallest length scales of 1 mm and do not simulate cloud chemistry in individual cloud droplets due to large computational costs. Here we incorporate the formation of isoprene epoxydiol SOA (IEPOX-SOA) in individual droplets within a one-dimensional explicit mixing parcel model (EMPM-Chem). We apply EMPM-Chem to simulate turbulence and droplet-resolved IEPOX-SOA formation using a configuration based on the Michigan Tech Pi chamber. We find that the dissolution of IEPOX gases is weighted more towards larger cloud droplets due to their large liquid water content (compared to smaller droplets), while the conversion of dissolved IEPOX to IEPOX-SOA is much greater within smaller deliquesced haze particles due to their higher acidity and ionic strengths compared to cloud droplets. We also find that as droplet residence times increase in the chamber, e.g., due to increasing ammonium bisulfate seed aerosol injection rates and/or increasing heights of the chamber, formation of IEPOX-SOA increases substantially. Thus, our EMPM-Chem model could be used to design future cloud chambers to maximize SOA production from cloud chemistry. We also apply the EMPM-Chem model to simulate how IEPOX-SOA formation evolves in individual cloud droplets within rising cloudy parcels in the atmosphere. We find that as subsaturated air is entrained into and turbulently mixed with the cloud parcel, evaporation causes a reduction in droplet sizes, which leads to corresponding increases in per droplet ionic strength and acidity. Increased droplet acidity in turn greatly accelerates the kinetics of IEPOX-SOA formation. In conclusion, our results provide key insights into single-cloud-droplet chemistry, suggesting that entrainment mixing may be an important process that increases SOA formation in the real atmosphere.
This study demonstrates the high-resolution profiling of cloud microphysics in a laboratory chamber using Time-Correlated Single Photon Counting (TCSPC) LiDAR. We present a novel retrieval method to derive vertical extinction (𝜎) profiles, constrained by in situ measurements, to diagnose responses to dry-air entrainment. In clean clouds, the LiDAR signals and retrieved 𝜎 remain relatively uniform, with entrainment effects confined to the upper layer. In contrast, polluted clouds exhibit strong vertical variability and a transition to a water-vapor-limited state. Entrainment significantly enhances the haze number concentration (𝑁ℎ), particularly near the bottom, creating highly height-dependent extinction profiles for polluted clouds. Our results highlight the capability of high-resolution LiDAR in capturing fine-scale vertical inhomogeneities. This approach provides a robust framework for quantifying how aerosol loading modulates entrainment sensitivity, offering new insights into the transition between buffered and water-vapor-limited regimes.
Radiance and polarization of multiple scattered light from haze and clouds
Radiance and polarization of multiple scattered light from haze and clouds calculated from Stokes vectors by Monte Carlo method
Photometric investigation of haze in Mars atmosphere revealed by Mariner 4 television data
Model explaining brightness and haze in Mars photographs obtained by Mariner 4 spacecraft
Mars surface features contrast reduction, discussing forward scattering haze as possible cause