No Arabic abstract
The Cassini mission to the Saturn system discovered a plume of ice grains and water vapor erupting from cracks on the icy surface of the satellite Enceladus. This moon has a global ocean in contact with a rocky core beneath its icy exterior, making it a promising location to search for evidence of extraterrestrial life in the solar system. The previous detection of H$_2$ in the plume indicates that there is free energy available for methanogenesis, the metabolic reaction of H$_2$ with CO$_2$ to form methane and water. Additional metabolic pathways could provide sources of energy in Enceladus ocean, but require the use of other oxidants that have not been detected in the plume. Here, we perform chemical modeling to determine how the production of radiolytic O$_2$ and H$_2$O$_2$, and abiotic redox chemistry in the ocean and rocky core, contribute to chemical disequilibria that could support metabolic processes in Enceladus ocean. We consider three possible cases for ocean redox chemistry: Case I in which reductants are not present in appreciable amounts and oxidants accumulate over time, and Cases II and III in which aqueous reductants or seafloor minerals, respectively, convert O$_2$ and H$_2$O$_2$ to SO$_4^{2-}$ and ferric oxyhydroxides. We calculate the upper limits on the concentrations of oxidants and chemical energy available for metabolic reactions in all three cases, neglecting additional abiotic reactions. For all three cases, we find that many aerobic and anaerobic metabolic reactions used by microbes on Earth could meet the minimum free energy threshold required for terrestrial life to convert ADP to ATP, as well as sustain positive cell density values within the Enceladus seafloor and/or ocean. These findings indicate that oxidant production and oxidation chemistry could contribute to supporting possible life and a metabolically diverse microbial community on Enceladus.
In the preceding paper (Efroimsky 2017), we derived an expression for the tidal dissipation rate in a homogeneous near-spherical Maxwell body librating in longitude. Now, by equating this expression to the outgoing energy flux due to the vapour plumes, we estimate the mean tidal viscosity of Enceladus, under the assumption that the Enceladean mantle behaviour is Maxwell. This method yields a value of $,0.24times 10^{14};mbox{Pa~s},$ for the mean tidal viscosity, which is very close to the viscosity of ice near the melting point.
Of profound astrobiological interest is that not only does Enceladus have a water ocean, but it also appears to be salty, important for its likely habitability. Here, we investigate how salinity affects ocean dynamics and equilibrium ice shell geometry and use knowledge of ice shell geometry and tidal heating rates to help constrain ocean salinity. We show that the vertical overturning circulation of the ocean, driven from above by melting and freezing and the temperature dependence of the freezing point of water on pressure, has opposing signs at very low and very high salinities. In both cases, heat and freshwater converges toward the equator, where the ice is thick, acting to homogenize thickness variations. In order to maintain observed ice thickness variations, ocean heat convergence should not overwhelm heat loss rates through the equatorial ice sheet. This can only happen when the oceans salinity has intermediate values, order $20$~psu. In this case polar-sinking driven by meridional temperature variations is largely canceled by equatorial-sinking circulation driven by salinity variations and a consistent ocean circulation, ice shell geometry and tidal heating rate can be achieved.
The metabolic processes complexity is at the heart of energy conversion in living organisms and forms a huge obstacle to develop tractable thermodynamic metabolism models. By raising our analysis to a higher level of abstraction, we develop a compact -- i.e. relying on a reduced set of parameters -- thermodynamic model of metabolism, in order to analyze the chemical-to-mechanical energy conversion under muscle load, and give a thermodynamic ground to Hills seminal muscular operational response model. Living organisms are viewed as dynamical systems experiencing a feedback loop in the sense that they can be considered as thermodynamic systems subjected to mixed boundary conditions, coupling both potentials and fluxes. Starting from a rigorous derivation of generalized thermoelastic and transport coefficients, leading to the definition of a metabolic figure of merit, we establish the expression of the chemical-mechanical coupling, and specify the nature of the dissipative mechanism and the so called figure of merit. The particular nature of the boundary conditions of such a system reveals the presence of a feedback resistance, representing an active parameter, which is crucial for the proper interpretation of the muscle response under effort in the framework of Hills model. We also develop an exergy analysis of the so-called maximum power principle, here understood as a particular configuration of an out-of-equilibrium system, with no supplemental extremal principle involved.
The ice shell on Enceladus, an icy moon of Saturn, exhibits strong asymmetry between the northern and southern hemispheres, with all known geysers concentrated over the south pole, even though the expected pattern of tidal-rotational deformation should be symmetric between the north and south poles. Using an idealized ice evolution model, we demonstrate that this asymmetry may form spontaneously, without any noticeable a priori asymmetry (such as a giant impact or a monopole structure of geological activity), in contrast to previous studies. Infinitesimal asymmetry in the ice shell thickness due to random perturbations are found to be able to grow indefinitely, ending up significantly thinning the ice shell at one of the poles, thereby allowing fracture formation there. Necessary conditions to trigger this hemispheric symmetry breaking mechanism are found analytically. A rule of thumb we find is that, for Galilean and Saturnian icy moons, the ice shell can undergo hemispheric symmetry breaking only if the mean shell thickness is around 10-30~km.
Quantitative scaling relationships among body mass, temperature and metabolic rate of organisms are still controversial, while resolution may be further complicated through the use of different and possibly inappropriate approaches to statistical analysis. We propose the application of a modelling strategy based on Akaikes information criteria and non-linear model fitting (nlm). Accordingly, we collated and modelled available data at intraspecific level on the individual standard metabolic rate of Antarctic microarthropods as a function of body mass (M), temperature (T), species identity (S) and high rank taxa to which species belong (G) and tested predictions from Metabolic Scaling Theory. We also performed allometric analysis based on logarithmic transformations (lm). Conclusions from lm and nlm approaches were different. Best-supported models from lm incorporated T, M and S. The estimates of the allometric scaling exponent b linking body mass and metabolic rate indicated no interspecific difference and resulted in a value of 0.696 +/- 0.105 (mean +/- 95% CI). In contrast, the four best-supported nlm models suggested that both the scaling exponent and activation energy significantly vary across the high rank taxa to which species belong, with mean values of b ranging from about 0.6 to 0.8. We therefore reached two conclusions: 1) published analyses of arthropod metabolism based on logarithmic data may be biased by data transformation; 2) non-linear models applied to Antarctic microarthropod metabolic rate suggest that intraspecific scaling of standard metabolic rate in Antarctic microarthropods is highly variable and can be characterised by scaling exponents that greatly vary within taxa, which may have biased previous interspecific comparisons that neglected intraspecific variability.