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Hydrodynamic Escape of Hot Protoatmospheres During a Star’s X-ray and Extreme Ultraviolet Saturation May Limit Rocky Exoplanets to ~1.8 Earth Radii

ABSTRACT: Recent observations and analysis of low mass (<10 M?), exoplanets have found that rocky planets only have radii up to 1.5–2 R?. Two general hypotheses exist for the cause of the dichotomy between rocky and gas-enveloped planets (or possible water worlds): either low mass planets do not necessarily form thick atmospheres of a few wt. %, or the thick atmospheres on these planets easily escape driven by x-ray and extreme ultraviolet (XUV) emissions from young parent stars. Here we show that a cutoff between rocky and gas-enveloped planets due to hydrodynamic escape is most likely to occur at a mean radius of 1.76±0.38 (2?) R? around Sun-like stars. We examine the limit in rocky planet radii predicted by hydrodynamic escape across a wide range of possible model inputs using 10,000 parameter combinations drawn randomly from plausible parameter ranges. We find a cutoff between rocky and gas-enveloped planets that agrees with the observed cutoff. The large cross-section available for XUV absorption in the extremely distended primitive atmospheres of low mass planets results in complete loss of atmospheres during the ~100 Myr phase of stellar XUV saturation. In contrast, more massive planets have less distended atmospheres and less escape, and so retain thick atmospheres through XUV saturation and then indefinitely as the XUV and escape fluxes drop over time. The agreement between our model and exoplanet data leads us to conclude that hydrodynamic escape plausibly explains the observed upper limit on rocky planet size and few planets (a “valley”) in the 1.5–2 R? range.

SUBMITTER: Lehmer O

PROVIDER: S-EPMC7545495 | biostudies-literature | 2017 Aug

REPOSITORIES: biostudies-literature

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Project description:There is no generally accepted value for the lower temperature limit for life on Earth. We present empirical evidence that free-living microbial cells cooling in the presence of external ice will undergo freeze-induced desiccation and a glass transition (vitrification) at a temperature between -10°C and -26°C. In contrast to intracellular freezing, vitrification does not result in death and cells may survive very low temperatures once vitrified. The high internal viscosity following vitrification means that diffusion of oxygen and metabolites is slowed to such an extent that cellular metabolism ceases. The temperature range for intracellular vitrification makes this a process of fundamental ecological significance for free-living microbes. It is only where extracellular ice is not present that cells can continue to metabolise below these temperatures, and water droplets in clouds provide an important example of such a habitat. In multicellular organisms the cells are isolated from ice in the environment, and the major factor dictating how they respond to low temperature is the physical state of the extracellular fluid. Where this fluid freezes, then the cells will dehydrate and vitrify in a manner analogous to free-living microbes. Where the extracellular fluid undercools then cells can continue to metabolise, albeit slowly, to temperatures below the vitrification temperature of free-living microbes. Evidence suggests that these cells do also eventually vitrify, but at lower temperatures that may be below -50°C. Since cells must return to a fluid state to resume metabolism and complete their life cycle, and ice is almost universally present in environments at sub-zero temperatures, we propose that the vitrification temperature represents a general lower thermal limit to life on Earth, though its precise value differs between unicellular (typically above -20°C) and multicellular organisms (typically below -20°C). Few multicellular organisms can, however, complete their life cycle at temperatures below ?-2°C.

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Hydrodynamic Escape of Hot Protoatmospheres During a Star’s X-ray and Extreme Ultraviolet Saturation May Limit Rocky Exoplanets to ~1.8 Earth Radii

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