No Arabic abstract
In an effort to derive temperature based criteria of habitability for multicellular life, we investigated the thermal limits of terrestrial poikilotherms, i.e. organisms whose body temperature and the functioning of all vital processes is directly affected by the ambient temperature. Multicellular poikilotherms are the most common and evolutionarily ancient form of complex life on earth. The thermal limits for their active metabolism and reproduction are bracketed by the temperature interval 0C<T<50C. The same interval applies to the photosynthetic production of oxygen, an essential ingredient of complex life, and for the generation of atmospheric biosignatures. Analysis of the main mechanisms responsible for the thermal thresholds of terrestrial life suggests that the same mechanisms would apply to other forms of chemical life. We propose a habitability index for complex life, h050, representing the mean orbital fraction of planetary surface that satisfies the temperature limits 0C<T<50C. With the aid of a climate model tailored for the calculation of the surface temperature of Earth-like planets, we calculated h050 as a function of planet insolation S, and atmospheric columnar mass Natm, for a few earth-like atmospheric compositions. By displaying h050 as a function of S and Natm, we built up an atmospheric mass habitable zone (AMHZ) for complex life. At variance with the classic habitable zone, the inner edge of the complex life HZ is not affected by the uncertainties inherent to the calculation of the runaway greenhouse limit. The complex life HZ is significantly narrower than the HZ of dry planets. Our calculations illustrate how changes in ambient conditions dependent on S and Natm, such as temperature excursions and surface dose of secondary particles of cosmic rays, may influence the type of life potentially present at different epochs of planetary evolution inside the AMHZ.
Habitability has been generally defined as the capability of an environment to support life. Ecologists have been using Habitat Suitability Models (HSMs) for more than four decades to study the habitability of Earth from local to global scales. Astrobiologists have been proposing different habitability models for some time, with little integration and consistency between them and different in function to those used by ecologists. In this white paper, we suggest a mass-energy habitability model as an example of how to adapt and expand the models used by ecologists to the astrobiology field. We propose to implement these models into a NASA Habitability Standard (NHS) to standardize the habitability objectives of planetary missions. These standards will help to compare and characterize potentially habitable environments, prioritize target selections, and study correlations between habitability and biosignatures. Habitability models are the foundation of planetary habitability science. The synergy between the methods used by ecologists and astrobiologists will help to integrate and expand our understanding of the habitability of Earth, the Solar System, and exoplanets.
With the discovery of hundreds of exoplanets and a potentially huge number of Earth-like planets waiting to be discovered, the conditions for their habitability have become a focal point in exoplanetary research. The classical picture of habitable zones primarily relies on the stellar flux allowing liquid water to exist on the surface of an Earth-like planet with a suitable atmosphere. However, numerous further stellar and planetary properties constrain habitability. Apart from geophysical processes depending on the internal structure and composition of a planet, a complex array of astrophysical factors additionally determine habitability. Among these, variable stellar UV, EUV, and X-ray radiation, stellar and interplanetary magnetic fields, ionized winds, and energetic particles control the constitution of upper planetary atmospheres and their physical and chemical evolution. Short- and long-term stellar variability necessitates full time-dependent studies to understand planetary habitability at any point in time. Furthermore, dynamical effects in planetary systems and transport of water to Earth-like planets set fundamentally important constraints. We will review these astrophysical conditions for habitability under the crucial aspects of the long-term evolution of stellar properties, the consequent extreme conditions in the early evolutionary phase of planetary systems, and the important interplay between properties of the host star and its planets.
Dozens of habitable zone, approximately earth-sized exoplanets are known today. An emerging frontier of exoplanet studies is identifying which of these habitable zone, small planets are actually habitable (have all necessary conditions for life) and, of those, which are earth-like. Many parameters and processes influence habitability, ranging from the orbit through detailed composition including volatiles and organics, to the presence of geological activity and plate tectonics. While some properties will soon be directly observable, others cannot be probed by remote sensing for the foreseeable future. Thus, statistical understanding of planetary systems formation and evolution is a key supplement to the direct measurements of planet properties. Probabilistically assessing parameters we cannot directly measure is essential to reliably assess habitability, to prioritizing habitable-zone planets for follow-up, and for interpreting possible biosignatures.
Habitability has been generally defined as the capability of an environment to support life. Ecologists have been using Habitat Suitability Models (HSMs) for more than four decades to study the habitability of Earth from local to global scales. Astrobiologists have been proposing different habitability models for some time, with little integration and consistency among them, being different in function to those used by ecologists. Habitability models are not only used to determine if environments are habitable or not, but they also are used to characterize what key factors are responsible for the gradual transition from low to high habitability states. Here we review and compare some of the different models used by ecologists and astrobiologists and suggest how they could be integrated into new habitability standards. Such standards will help to improve the comparison and characterization of potentially habitable environments, prioritize target selections, and study correlations between habitability and biosignatures. Habitability models are the foundation of planetary habitability science and the synergy between ecologists and astrobiologists is necessary to expand our understanding of the habitability of Earth, the Solar System, and extrasolar planets.
The nearby ultracool dwarf TRAPPIST-1 possesses several Earth-sized terrestrial planets, three of which have equilibrium temperatures that may support liquid surface water, making it a compelling target for exoplanet characterization. TRAPPIST-1 is an active star with frequent flaring, with implications for the habitability of its planets. Superflares (stellar flares whose energy exceeds 10^33 erg) can completely destroy the atmospheres of a cool stars planets, allowing ultraviolet radiation and high-energy particles to bombard their surfaces. However, ultracool dwarfs emit little ultraviolet flux when quiescent, raising the possibility of frequent flares being necessary for prebiotic chemistry that requires ultraviolet light. We combine Evryscope and Kepler observations to characterize the high-energy flare rate of TRAPPIST-1. The Evryscope is an array of 22 small telescopes imaging the entire Southern sky in g every two minutes. Evryscope observations, spanning 170 nights over 2 years, complement the 80-day continuous short-cadence K2 observations by sampling TRAPPIST-1s long-term flare activity. We update TRAPPIST-1s superflare rate, finding a cumulative rate of 4.2 (+1.9 -0.2) superflares per year. We calculate the flare rate necessary to deplete ozone in the habitable-zone planets atmospheres, and find that TRAPPIST-1s flare rate is insufficient to deplete ozone if present on its planets. In addition, we calculate the flare rate needed to provide enough ultraviolet flux to power prebiotic chemistry. We find TRAPPIST-1s flare rate is likely insufficient to catalyze some of the Earthlike chemical pathways thought to lead to RNA synthesis, and flux due to flares in the biologically relevant UV-B band is orders of magnitude less for any TRAPPIST-1 planet than has been experienced by Earth at any time in its history.