red dwarf stars
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Author(s):  
Vera G. Sinitsyna ◽  
Vera Yu. Sinitsyna ◽  
Yurii I. Stozhkov

Astrophysics ◽  
2019 ◽  
Vol 62 (2) ◽  
pp. 234-250 ◽  
Author(s):  
O. M. Belova ◽  
K. V. Bychkov

2018 ◽  
Vol 155 (5) ◽  
pp. 215 ◽  
Author(s):  
Brian D. Mason ◽  
William I. Hartkopf ◽  
Korie N. Miles ◽  
John P. Subasavage ◽  
Deepak Raghavan ◽  
...  

2016 ◽  
Vol 16 (1) ◽  
pp. 1-9 ◽  
Author(s):  
Joseph Gale ◽  
Amri Wandel

AbstractWe review the latest findings on extra-solar planets and their potential of having environmental conditions that could support Earth-like life. Focusing on planets orbiting red dwarf (RD) stars, the most abundant stellar type in the Milky Way, we show that including RDs as potential life supporting host stars could increase the probability of finding biotic planets by a factor of up to a thousand, and reduce the estimate of the distance to our nearest biotic neighbour by up to 10. We argue that binary and multiple star systems need to be taken into account when discussing habitability and the abundance of biotic exoplanets, in particular RDs in such systems. Early considerations indicated that conditions on RD planets would be inimical to life, as their habitable zones would be so close to the host star as to make planets tidally locked. This was thought to cause an erratic climate and expose life forms to flares of ionizing radiation. Recent calculations show that these negative factors are less severe than originally thought. It has also been argued that the lesser photon energy of the radiation of the relatively cool RDs would not suffice for oxygenic photosynthesis (OP) and other related energy expending reactions. Numerous authors suggest that OP on RD planets may evolve to utilize photons in the infrared. We however argue, by analogy to the evolution of OP and the environmental physiology and distribution of land-based vegetation on Earth, that the evolutionary pressure to utilize infrared radiation would be small. This is because vegetation on RD planets could enjoy continuous illumination of moderate intensity, containing a significant component of photosynthetic 400–700 nm radiation. We conclude that conditions for OP could exist on RD planets and consequently the evolution of complex life might be possible. Furthermore, the huge number and the long lifetime of RDs make it more likely to find planets with photosynthesis and life around RDs than around Solar type stars.


2015 ◽  
Vol 357 (2) ◽  
Author(s):  
E. Morchenko ◽  
K. Bychkov ◽  
M. Livshits

Author(s):  
Ignas Snellen

Ground-based high-dispersion spectroscopy could reveal molecular oxygen as a biomarker gas in the atmospheres of twin-Earths transiting red dwarf stars within the next 25 years. The required contrasts are only a factor of 3 lower than that already achieved for carbon monoxide in hot Jupiter atmospheres today but will need much larger telescopes because the target stars will be orders of magnitude fainter. If extraterrestrial life is very common and can therefore be found on planets around the most nearby red dwarf stars, it may be detectable via transmission spectroscopy with the next-generation extremely large telescopes. However, it is likely that significantly more collecting area is required for this. This can be achieved through the development of low-cost flux collector technology, which combines a large collecting area with a low but sufficient image quality for high-dispersion spectroscopy of bright stars.


2014 ◽  
Vol 83 (4) ◽  
pp. 449-464
Author(s):  
Michael N. Mautner

Astroecology concerns the relations between life and space resources, and cosmo-ecology extrapolates these relations to cosmological scales. Experimental astroecology can quantify the amounts of life that can be derived from space resources. For this purpose, soluble carbon and electrolyte nutrients were measured in asteroid/meteorite materials. Microorganisms and plant cultures were observed to grow on these materials, whose fertilities are similar to productive agricultural soils. Based on measured nutrient contents, the 10<sup>22</sup> kg carbonaceous asteroids can yield 10<sup>18</sup> kg biomass with N and P as limiting nutrients (compared with the estimated 10<sup>15</sup> kg biomass on Earth). These data quantify the amounts of life that can be derived from asteroids in terms of time-integrated biomass [<em>BIOTA</em><sub>int</sub> = biomass (kg) × lifetime (years)], as 10<sup>27</sup> kg-years during the next billion years of the Solar System (a thousand times the 10<sup>24</sup> kg-years to date). The 10<sup>26</sup> kg cometary materials can yield biota 10 000 times still larger. In the galaxy, potential future life can be estimated based on stellar luminosities. For example, the Sun will develop into a white dwarf star whose 10<sup>15</sup> W luminosity can sustain a <em>BIOTA</em><sub>int</sub> of 10<sup>34</sup> kg-years over 10<sup>20</sup> years. The 10<sup>12</sup> main sequence and white and red dwarf stars can sustain 10<sup>46</sup> kg-years of <em>BIOTA</em><sub>int</sub> in the galaxy and 10<sup>57</sup> kg-years in the universe. Life has great potentials in space, but the probability of present extraterrestrial life may be incomputable because of biological and ecological complexities. However, we can establish and expand life in space with present technology, by seeding new young solar systems. Microbial representatives of our life-form can be launched by solar sails to new planetary systems, including extremophiles suited to diverse new environments, autotrophs and heterotrophs to continually form and recycle biomolecules, and simple multicellulars to jump-start higher evolution. These programs can be motivated by life-centered biotic ethics that seek to secure and propagate life. In space, life can develop immense populations and diverse new branches. Some may develop into intelligent species that can expand life further in the galaxy, giving our human endeavors a cosmic purpose.


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