Abstract
We present a model for the internal structure of Saturn’s moon Enceladus. This model allows us to estimate the physical conditions at the bottom of the satellite’s potential subsurface water reservoir and to determine the radial distribution of pressure and gravity. This leads to a better understanding of the physical and chemical conditions at the water/rock boundary. This boundary is the most promising area on icy moons for astrobiological studies as it could serve as a potential habitat for extraterrestrial life similar to terrestrial microbes that inhabit rocky mounds on Earth’s sea floors.
Similar content being viewed by others
Introduction
From the astrobiological point of view, icy moons are among the most interesting objects in the Solar System. Some of these moons could have subsurface oceans which may host extraterrestrial life. In this study we present a model for the interior structure of the icy moon Enceladus and discuss its potential habitability. Enceladus provides a unique insight into its interior through its active plumes which may originate in a potential subsurface sea (Postberg et al. 2009). The small mean radius of only 252.1 km (Thomas 2010) (for further parameters, see Table 1) indicates that the uncompressed density (see, e.g., Faure and Mensing 2007) of the satellite is almost equal to its bulk density, so a simplified model of Enceladus’ interior is reasonable.
Previous studies of Enceladus’ interior (e.g., Barr and McKinnon 2007; Hussmann et al. 2006; McKinnon 2015; Roberts 2015; Schubert et al. 2007) assumed a two-layer structure with a rocky core (core density ρ c between 2500 and 3527.5 kg m −3) and an icy outer shell (shell density ρ s ≈ 1000 kg m −3). These estimations led to an ice shell thickness of approximately 100 km and a moment of inertia factor (MoI) of around 0.31. On the other hand, Rappaport et al. assumed a hydrated silicate core with ρ c ≈ 2500 kg m −3 which results in an ice shell thickness of just 60 km (Rappaport et al. 2007). According to the latest gravity measurements performed by the NASA spacecraft Cassini, Enceladus has a high MoI of 0.335 (Iess et al. 2014), which leads to the conclusion that this satellite is not in a fully relaxed shape, but is differentiated with a low-density core.
Model
2-Layer-Model
The MoI of Enceladus can be estimated using the Radau-Darwin approximation (see, e.g., Schubert et al. 2004):
where \(k_{2} = \frac {4 C_{22} GM}{\omega ^{2} R^{3}}=0.9896 \pm 0.0103\) is the fluid potential Love number. Therefore, Enceladus has a MoI of 0.3386 ± 0.0826. This is in agreement with the study by Iess et al. where the moment of inertia factor was estimated to be around 0.335 (Iess et al. 2014). Because this value is less than 0.4, it also falls under the maximum MoI for a differentiated body (de Pater and Lissauer 2010).
Enceladus’ mean radius R, its mean density \(\bar {\rho }\), and the calculated MoI serve as the starting points for our model. Because of the low mass of Enceladus and the resulting low radial pressure values, the density can be assumed to be constant within a certain layer. To calculate the core mean density ρ c and core radius R c , we use a 2-layer-model (see, e.g., Hussmann et al. 2006):
We varied the composition, and therefore the density ρ s of the overlying water/ice shell between 917 kg m −3 (pure ice I) and 1 080 kg m −3 (water with some other constituents such as NH 3 and tholins (Hendrix et al. 2010)). To illustrate our results we selected three different cases (C m i n , C m e a n , and C m a x ; see Table 2).
Local Southern Subsurface Sea
According to previous studies, either a local subsurface water reservoir beneath the South Polar Terrain (SPT) of Enceladus (e.g., Iess et al. 2014) or a global ocean with a thinned out ice shell at the southern region (Thomas et al. 2015) seems likely. Therefore, the second aim of our model is to estimate the pressure at the water/rock-boundary of this potential aquifer beneath Encealdus’ southern region. We assume the sea or the depletion, respectively, to have the shape of a rotational paraboloid. For each of the cases C m i n , C m e a n , and C m a x (Table 2) we calculated the pressure at the water/rock boundary depending on the longitude and the maximum depth of the subsurface aquifer. As seen in Fig. 1 for C m e a n and in Table 3 for all three cases, the pressure value at the sea floor of the potential subsurface water reservoir lies between 28 and 45 bar.
Radial Pressure Gradient
We also calculated the radial distributions of pressure (d p = ρ⋅g(r)d r) and gravitational acceleration (\(g(r) =\frac {G M(r)}{r^{2}}\)) for case C m e a n with a subsurface water aquifer 10 km thick (see Fig. 2). Under these assumptions we obtained a pressure at the core/water-boundary of 32.9 ⋅105Pa and a gravitational acceleration of 0.128 ms −2.
To validate this model we applied it to the different layers of Earth. Gravitational acceleration as well as the pressure gradient in the outer layers obtained by our model agree well with the Preliminary Reference Earth Model (PREM, Dziewonski and Anderson1981), but the pressure values for Earth’s inner core are too small. This deviation is due to the exclusion of compression or phase transition effects from our model, as these effects are negligible for small bodies like Enceladus where the uncompressed density is equal to the bulk density.
Conclusion
The most promising area on Enceladus where life may exist is at the sea floor of the potential subsurface water reservoir. Geochemical low-temperature interactions between these layers seem reasonable (see, e.g., Zolotov 2007). One of these processes may be serpentinization of ultramafic rocks which is accompanied by the production of H 2 (Schrenk et al. 2013). Furthermore, in such an environment dissolution of minerals could provide nutrients for possible lifeforms.
The organisms would have to be able to live without photosynthesis or its by-products such as oxygen. According to McKay et al., there are three known terrestrial microbial ecosystems that would fit into such a habitat (McKay et al. 2008): two are based on methanogens and the third is built on sulphur-reducing bacteria. However, the existence of sulphur-reducing bacteria is questionable because oxidized sulphur may not exist on Enceladus, which limits/excludes the process of sulphur (sulphate) reduction.
In further experimental studies, we will investigate the habitability of the subsurface water aquifer. In accordance with our model, microorganisms would have to resist a pressure of approximately 28 to 45 bar (equivalent to 2.8 to 4.5 MPa, see Table 3), which is roughly equivalent to the pressure at a depth of 290 to 460 m below sea level on Earth. Microorganisms tolerant to such pressures (and higher) are well known on Earth, e.g., the barotolerant bacteria S. hanedai IAM12641 (optimal growth at 0.1 MPa, (MacDonell and Colwell 1985)) or even obligate barophilic microbes such as M. yayanosii DB21MT-5 which was isolated from the Mariana Trench and for which no growth was detected at pressures of less than 50 MPa (Kato et al. 1998). Even multicellular organisms like deep-sea fish and worms can easily resist the pressure at this depth in the terrestrial seas, e.g., the hadal snailfish Pseudoliparis amblystomopsis which was even found at a depth of 8145 m in the Mariana Trench (Morelle 2014).
To conclude, pressure should not be a limiting parameter for life in Enceladus’ subsurface sea.
References
Barr AC, McKinnon WB (2007) Convection in Enceladus’ ice shell: conditions for initiation. Geophys Res Lett 34:9
de Pater I, Lissauer JJ (2010) Planetary sciences, vol 33. Cambridge University Press, Cambridge
Dziewonski AM, Anderson DL (1981) Preliminary reference Earth model. Phys Earth Planet In 25:297–356
Faure G, Mensing TM (2007) Introduction to planetary science: the geological perspective, vol 28-32. Springer, Netherlands
Hussmann H, Sohl F, Spohn T (2006) Subsurface oceans and deep interiors of medium-sized outer planet satellites and large trans-neptunian objects. Icarus 185:258–273
Hendrix A et al. (2010) The ultraviolet reflectance of Enceladus: implications for surface composition. Icarus 206:608–617
Iess L et al. (2014) The gravity field and interior structure of Enceladus. Science 344:78–80
Jacobson RA (2010) SAT339 - JPL satellite ephemeris
Kato C et al. (1998) Extremely barophilic bacteria isolated from the Mariana Trench, challenger deep, at a depth of 11000 meters. Appl Environ Microbiol 64:1510–1513
MacDonell MT, Colwell RR (1985) Phylogeny of the Vibrionaceae and recommendation for two new genera Listonella and Shewanella. Syst Appl Microbiol 6:171–182
McKay CP et al. (2008) The possible origin and persistence of life on Enceladus and detection of biomarkers in the Plume. Astrobiology 8:909–919
Roberts JH (2015) The fluffy core of Enceladus. Icarus 258:54–66
Morelle R (2014) New record for deepest fish, BBC News, 19/12/2014. http://www.bbc.com/news/science-environment-30541065
Postberg F et al. (2009) Sodium salts in E-ring ice grains from an ocean below the surface of Enceladus. Nature 459:1098–1101
Rappaport NJ et al. (2007) Mass and interior of Enceladus from Cassini data analysis. Icarus 190:175–178
McKinnon WB (2015) Effect of Enceladus’s rapid synchronous spin on interpretation of Cassini gravity. Geophys Res Lett 42:2137–2143
Schrenk MO et al. (2013) Serpentinization, carbon, and deep life. Rev Mineral Geochem 75:575–606
Schubert G et al. (2004) Jupiter: the planet, satellites and magnetosphere, 281-306. Cambridge planetary science, vol 1. Cambridge University Press, Cambridge
Schubert G et al. (2007) Enceladus: present internal structure and differentiation by early and long-term radiogenic heating. Icarus 188:345–355
Taubner R-S (2012) The possibility of the existence of a nitrogen cycle within Enceladus. Master Thesis, University of Vienna
Thomas PC (2010) Sizes, shapes, and derived properties of the saturnian satellites after the Cassini nominal mission. Icarus 208:395–401
Thomas PC et al. (2015) Enceladus’s measured physical libration requires a global subsurface ocean. Icarus 264:37–47
Zolotov MY (2007) An oceanic composition on early and today’s Enceladus. Geophys Res Lett 34:L23203
Acknowledgments
We acknowledge financial support of this study by the University of Vienna in the framework of Research Platform ExoLife (FPF-234).
Author information
Authors and Affiliations
Corresponding author
Additional information
This paper is part of the Special Collection of Papers from EANA 2013: The 13th European Workshop on Astrobiology, 22-25 July 2013, Szczecin, Poland (Franco Ferrari and Ewa Szuszkiewicz Guest Editors)
Rights and permissions
About this article
Cite this article
Taubner, RS., Leitner, J.J., Firneis, M.G. et al. Modelling the Interior Structure of Enceladus Based on the 2014’s Cassini Gravity Data. Orig Life Evol Biosph 46, 283–288 (2016). https://doi.org/10.1007/s11084-015-9475-9
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11084-015-9475-9