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In this hypothesis article, we discuss the basic requirements of planetary environments where aerobe organisms can grow and survive, including atmospheric limitations of millimeter-to-meter-sized biological animal life based on physical limits and O 2 , N 2 , and CO 2 toxicity levels. By assuming that animal-like extraterrestrial organisms adhere to similar limits, we define Earth-like habitats (EH) as rocky exoplanets in the habitable zone for complex life that host N 2 -O 2 -dominated atmospheres with minor amounts of CO 2 , at which advanced animal-like life or potentially even extraterrestrial intelligent life can in principle evolve and exist. We then derive a new formula that can be used to estimate the maximum occurrence rate of such Earth-like habitats in the Galaxy. This contains realistic probabilistic arguments that can be fine-tuned and constrained by atmospheric characterization with future space and ground-based telescopes. As an example, we briefly discuss two specific requirements feeding into our new formula that, although not quantifiable at present, will become scientifically quantifiable in the upcoming decades due to future observations of exoplanets and their atmospheres. Key Words: Eta-Earth-Earth-like habitats-oxygenation time-nitrogen atmospheres-carbon dioxide-animal-like life. Astrobiology 24, 897-915.

In Lammer et al. (2024), we defined Earth-like habitats (EHs) as rocky exoplanets within the habitable zone of complex life (HZCL) on which Earth-like N 2 -O 2 -dominated atmospheres with minor amounts of CO 2 can exist, and derived a formulation for estimating the maximum number of EHs in the galaxy given realistic probabilistic requirements that have to be met for an EH to evolve. In this study, we apply this formulation to the galactic disk by considering only requirements that are already scientifically quantifiable. By implementing literature models for star formation rate, initial mass function, and the mass distribution of the Milky Way, we calculate the spatial distribution of disk stars as functions of stellar mass and birth age. For the stellar part of our formulation, we apply existing models for the galactic habitable zone and evaluate the thermal stability of nitrogen-dominated atmospheres with different CO 2 mixing ratios inside the HZCL by implementing the newest stellar evolution and upper atmosphere models. For the planetary part, we include the frequency of rocky exoplanets, the availability of surface water and subaerial land, and the potential requirement of hosting a large moon by evaluating their importance and implementing these criteria from minima to maxima values as found in the scientific literature. We also discuss further factors that are not yet scientifically quantifiable but may be requirements for EHs to evolve. Based on such an approach, we find that EHs are relatively rare by obtaining plausible maximum numbers of 2.5 - 2.4 + 71.6 × 10 5 and 0.6 - 0.59 + 27.1 × 10 5 planets that can potentially host N 2 -O 2 -dominated atmospheres with maximum CO 2 mixing ratios of 10% and 1%, respectively, implying that, on average, a minimum of ∼ 10 3 - 10 6 rocky exoplanets in the HZCL are needed for 1 EH to evolve. The actual number of EHs, however, may be substantially lower than our maximum ranges since several requirements with unknown occurrence rates are not included in our model ( e.g. , the origin of life, working carbon-silicate and nitrogen cycles); this also implies extraterrestrial intelligence (ETI) to be significantly rarer still. Our results illustrate that not every star can host EHs nor can each rocky exoplanet within the HZCL evolve such that it might be able to host complex animal-like life or even ETIs. The Copernican Principle of Mediocrity therefore cannot be applied to infer that such life will be common in the galaxy.

The amount of nitrogen (N 2 ) present in the atmosphere when life evolved on our planet is central for understanding the production of prebiotic molecules and, hence, is a fundamental quantity to constrain. Estimates of atmospheric molecular nitrogen partial surface pressures during the Archean, however, widely vary in the literature. In this study, we apply a model that combines newly gained insights into atmospheric escape, magma ocean duration, and outgassing evolution. Results suggest <420 mbar surface molecular nitrogen at the time when life originated, which is much lower compared with estimates in previous works and hence could impact our understanding of the production rate of prebiotic molecules such as hydrogen cyanide. Our revised values provide new input for atmospheric chamber experiments that simulate prebiotic chemistry on the early Earth. Our results that assume negligible nitrogen escape rates are in agreement with research based on solidified gas bubbles and the oxidation of iron in micrometeorites at 2.7 Gyr ago, which suggest that the atmospheric pressure was probably less than half the present-day value. Our results contradict previous studies that assume N 2 partial surface pressures during the Archean were higher than those observed today and suggest that, if the N 2 partial pressure were low in the Archean, it would likely be low in the Hadean as well. Furthermore, our results imply a biogenic nitrogen fixation rate from 9 to 14 Teragram N 2 per year (Tg N 2 /year), which is consistent with modern marine biofixation rates and, hence, indicate an oceanic origin of this fixation process.

Since the Archean, N 2 has been a major atmospheric constituent in Earth's atmosphere. Nitrogen is an essential element in the building blocks of life; therefore, the geobiological nitrogen cycle is a fundamental factor in the long-term evolution of both Earth and Earth-like exoplanets. We discuss the development of Earth's N 2 atmosphere since the planet's formation and its relation with the geobiological cycle. Then we suggest atmospheric evolution scenarios and their possible interaction with life-forms: first for a stagnant-lid anoxic world, second for a tectonically active anoxic world, and third for an oxidized tectonically active world. Furthermore, we discuss a possible demise of present Earth's biosphere and its effects on the atmosphere. Since life-forms are the most efficient means for recycling deposited nitrogen back into the atmosphere at present, they sustain its surface partial pressure at high levels. Also, the simultaneous presence of significant N 2 and O 2 is chemically incompatible in an atmosphere over geological timescales. Thus, we argue that an N 2 -dominated atmosphere in combination with O 2 on Earth-like planets within circumstellar habitable zones can be considered as a geo-biosignature. Terrestrial planets with such atmospheres will have an operating tectonic regime connected with an aerobic biosphere, whereas other scenarios in most cases end up with a CO 2 -dominated atmosphere. We conclude with implications for the search for life on Earth-like exoplanets inside the habitable zones of M to K stars.