We find that variations in the UV emissions of cool M-dwarf stars have a potentially large impact upon atmospheric biosignatures in simulations of Earth-like exoplanets i.e. planets with Earths development, and biomass and a molecular nitrogen-oxygen
dominated atmosphere. Starting with an assumed black-body stellar emission for an M7 class dwarf star, the stellar UV irradiation was increased stepwise and the resulting climate-photochemical response of the planetary atmosphere was calculated. Results suggest a Goldilocks effect with respect to the spectral detection of ozone. At weak UV levels, the ozone column was weak (due to weaker production from the Chapman mechanism) hence its spectral detection was challenging. At strong UV levels, ozone formation is stronger but its associated stratospheric heating leads to a weakening in temperature gradients between the stratosphere and troposphere, which results in weakened spectral bands. Also, increased UV levels can lead to enhanced abundances of hydrogen oxides which oppose the ozone formation effect. At intermediate UV (i.e. with x10 the stellar UV radiative flux of black body Planck curves corresponding to spectral class M7) the conditions are just right for spectral detection. Results suggest that the planetary O3 profile is sensitive to the UV output of the star from about(200-350) nm. We also investigated the effect of increasing the top-of-atmosphere incoming Lyman-alpha radiation but this had only a minimal effect on the biosignatures since it was efficiently absorbed in the uppermost planetary atmospheric layer, mainly by abundant methane. Earlier studies have suggested that the planetary methane is an important stratospheric heater which critically affects the vertical temperature gradient, hence the strength of spectral emission bands.
Understanding whether M-dwarf stars may host habitable planets with Earth-like atmospheres and biospheres is a major goal in exoplanet research. If such planets exist, the question remains as to whether they could be identified via spectral signature
s of biomarkers. Such planets may be exposed to extreme intensities of cosmic rays that could perturb their atmospheric photochemistry. Here, we consider stellar activity of M-dwarfs ranging from quiet up to strong flaring conditions and investigate one particular effect upon biomarkers, namely, the ability of secondary electrons caused by stellar cosmic rays to break up atmospheric molecular nitrogen (N2), which leads to production of nitrogen oxides in the planetary atmosphere, hence affecting biomarkers such as ozone. We apply a stationary model, that is, without a time-dependence, hence we are calculating the limiting case where the atmospheric chemistry response time of the biomarkers is assumed to be slow and remains constant compared with rapid forcing by the impinging stellar flares. This point should be further explored in future work with time-dependent models. For the flaring case O3 is mainly destroyed via direct titration with nitrogen oxides and not via the familiar catalytic cycle photochemistry, which occurs on Earth. For scenarios with low O3, Rayleigh scattering by the main atmospheric gases became more important for shielding the planetary surface from ultra-violet radiation. A major result of this work is that the biomarker O3 survived all the stellar-activity scenarios considered except for the strong case, whereas the biomarker nitrous oxide could survive in the planetary atmosphere under all conditions of stellar activity considered here, which clearly has important implications for missions that aim to detect spectroscopic biomarkers.
The search for life beyond the Solar System is a major activity in exoplanet science. However, even if an Earth-like planet were to be found, it is unlikely to be at a similar stage of evolution as the modern Earth. It is therefore of interest to inv
estigate the sensitivity of biomarker signals for life as we know it for an Earth-like planet but at earlier stages of evolution. Here, we assess biomarkers i.e. species almost exclusively associated with life, in present-day and in 10% present atmospheric level oxygen atmospheres corresponding to the Earths Proterozoic period. We investigate the impact of proposed enhanced microbial emissions of the biomarker nitrous oxide, which photolyses to form nitrogen oxides which can destroy the biomarker ozone. A major result of our work is regardless of the microbial activity producing nitrous oxide in the early anoxic ocean, a certain minimum ozone column can be expected to persist in Proterozoic-type atmospheres due to a stabilising feedback loop between ozone, nitrous oxide and the ultraviolet radiation field. Atmospheric nitrous oxide columns were enhanced by a factor of 51 for the Proterozoic Canfield ocean scenario with 100 times increased nitrous oxide surface emissions. In such a scenario nitrous oxide displays prominent spectral features, so may be more important as a biomarker than previously considered in such cases. The run with Canfield ocean nitrous oxide emissions enhanced by a factor of 100 also featured additional surface warming of 3.5K. Our results suggest that the Proterozoic ozone layer mostly survives the changes in composition which implies that it is indeed a good atmospheric biomarker.
After Earths origin, our host star, the Sun, was shining 20 to 25 percent less brightly than today. Without greenhouse-like conditions to warm the atmosphere, our early planet would have been an ice ball and life may never have evolved. But life did
evolve, which indicates that greenhouse gases must have been present on early Earth to warm the planet. Evidence from the geologic record indicates an abundance of the greenhouse gas CO2. CH4 was probably present as well, and in this regard methanogenic bacteria, which belong to a diverse group of anaerobic procaryotes that ferment CO 2 plus H2 to CH4, may have contributed to modification of the early atmosphere. Molecular oxygen was not present, as is indicated by the study of rocks from that era, which contain iron carbonate rather than iron oxide. Multicellular organisms originated as cells within colonies that became increasingly specialized. The development of photosynthesis allowed the Suns energy to be harvested directly by life forms. The resultant oxygen accumulated in the atmosphere and formed the ozone layer in the upper atmosphere. Aided by the absorption of harmful UV radiation in the ozone layer, life colonized Earths surface. Our own planet is a very good example of how life forms modified the atmosphere over the planets life time. We show that these facts have to be taken into account when we discover and characterize atmospheres of Earth-like exoplanets. If life has originated and evolved on a planet, then it should be expected that a strong co-evolution occurred between life and the atmosphere, the result of which is the planets climate.
