Search

Ancient Venus and Earth may have been similar in crucial ways for the development of life, such as liquid water oceans, land-ocean interfaces, favorable chemical ingredients and energy pathways. If life ever developed on, or was transported to, early Venus from elsewhere, it might have thrived, expanded and then survived the changes that have led to an inhospitable surface on Venus today. The Venus cloud layer may provide a refugium for extant life that persisted from an earlier more habitable surface environment. We introduce the Venus Life Equation - a theory and evidence-based approach to calculate the probability of extant life on Venus, L, using three primary factors of life: Origination, Robustness, and Continuity, or L = O x R x C. We evaluate each of these factors using our current understanding of Earth and Venus environmental conditions from the Archaean to the present. We find that the probability of origination of life on Venus would be similar to that of the Earth and argue that the other factors should be nonzero, comparable to other promising astrobiological targets in the solar system. The Venus Life Equation also identifies poorly understood aspects of Venus that can be addressed by direct observations with future exploration missions., Revision resubmitted after review to Astrobiology for Venus Special issue. 37 pages, 4 figures. Shorter version submitted as white paper in shortened form to Planetary and Astrobiology Decadal Survey

The interest in the possibility of life on Venus is driven not just by curiosity about life originating in another Earth-like environment, but because of the possibility that life may be playing a critical role in the planet’s present, and possibly its past, atmospheric state. The brilliance of Venus in the night sky (as viewed from Earth) is due to its highly reflective cloud cover, about 28 km thick at the equator. Its spectral albedo is about 90% at wavelengths > 500 nm, but it drops gradually to about 40% around 370 nm before rising slightly at shorter wavelengths. This albedo drop is due to the presence of several absorbers in the atmosphere and the cloud cover. A very large fraction of the energy absorbed by Venus is at ultraviolet wavelengths with sulfur dioxide above the clouds contributing to the absorption below 330 nm; however, the identities of the other absorbers remain unknown. The inability to identify the absorbers that are responsible for determining the radiative energy balance of Venus over the last century is a major impediment to understanding how the planet “works”, a major component of NASA’s efforts in planetary exploration. Limaye et al. (Astrobiology 18, 1181-1198, 2018) presented a hypothesis suggesting that cloud-based microbial life could be contributors to the spectral signatures of Venus’ clouds, building upon previous suggestions of the possibility of life in the clouds of Venus.Four interconnected themes for the exploration of Venus as an astrobiology target are: – (i) investigations focused on the likelihood that liquid water existed on the surface in the past leading to the potential for the origin and evolution of life, (ii) investigations into the potential for habitable zones within Venus’ clouds and Venus-like atmospheres, (iii) theoretical investigations into how active aerobiology may impact the radiative energy balance of Venus’ clouds and Venus-like atmospheres, and (iv) application of these investigative themes towards better understanding the atmospheric dynamics and habitability of exoplanets. These themes can serve as a basis for proposed Venus Astrobiology Objectives and suggestions for measurements for future missions, as per the goals and objectives developed by the Venus Exploration Analysis Group (VEXAG), which is sponsored by NASA to plan for the future exploration of Venus. A Venus Collection to be published in Astrobiology journal in 2021 will include papers from the “Habitability of the Venus Cloud Layer”, Moscow (October 2019) workshop.

International audience; More than 85% of the 23 investigations developed by VEXAG are largely accomplished via a NF mission centered on a variable-altitude balloon (aerobot) supported by a science/comm orbiter. Circling Venus >15 times over ~90 days, the aerobot repeatedly visits 52-62 km alts as it semi-continuously samples a host of environmental & surface parameters.

Understanding Venus will benefit from a dedicated effort through an international program of missions that are coordinated and offering opportunities for coooperation. The recent discovery of phosphene in the Venus clouds and possibility of life will increase the exploration missions and cooperation and coordination will be very benefical.

We present a case for the exploration of Venus as an astrobiology target—(1) investigations focused on the likelihood that liquid water existed on the surface in the past, leading to the potential for the origin and evolution of life, (2) investigations into the potential for habitable zones within Venus’ present-day clouds and Venus-like exo atmospheres, (3) theoretical investigations into how active aerobiology may impact the radiative energy balance of Venus’ clouds and Venus-like atmospheres, and (4) application of these investigative approaches toward better understanding the atmospheric dynamics and habitability of exoplanets. The proximity of Venus to Earth, guidance for exoplanet habitability investigations, and access to the potential cloud habitable layer and surface for prolonged in situ extended measurements together make the planet a very attractive target for near term astrobiological exploration.

We show that a spacecraft launched from Earth towards Mars following a Hohmann minimum energy transfer trajectory has a strong tendency to remain well-connected magnetically to Earth, in the early phase of the transfer, or to Mars in the late phase, via the Parker spiral magnetic field. On the return trip, the spacecraft would remain reasonably well-connected magnetically first to Mars and later to Earth. Moreover, good magnetic connectivity occurs on all Hohmann transfers between neighboring planets in the inner solar system out to Mars. We call this hitherto unnamed circumstance the Hohmann–Parker effect. We show consequences of the effect by means of simultaneous cosmic radiation proxy observations made near Earth, near Mars, and at the Mars Science Laboratory on the transfer from Earth to Mars in 2011/2012. We support the observations with simulations of the large-scale magnetic field of the inner heliosphere during this period and compare the results with our predictions. The implications of the Hohmann–Parker effect are discussed. & 2013 Published by Elsevier Ltd.

The equilibrium suggested as a buffer for CO2 in the Venus atmosphere, CaCO3 + SiO2 = CaSiO3 + CO2, cannot act as a buffer at the Venus surface/troposphere – the pressure–temperature slope of the equilibrium and that of the atmosphere (dry adiabat with significant greenhouse heating) do not provide buffering capacity (if indeed CaCO3 were present). Instead, perturbations to T or P(CO2) can produce catastrophic expansion or collapse of the atmosphere. This instability can be generalized to all devolatilization reactions that produce a radiatively active gas in a planetary atmosphere dominated by such gases, and gives a simple thermochemical criterion for whether a reaction could buffer such an atmosphere. Simple decarbonation reactions fail this criterion, suggesting that the abundance of CO2 in a CO2-dominated atmosphere cannot be buffered by chemical reactions with the surface; a similar conclusion holds for the abundance of H2O in an H2O-dominated (steam) atmosphere. Buffering of minor gases is more likely; a mineral buffer equilibrium for SO2 proposed for Venus, FeS2 + CO2 = Fe3O4 + SO2 + CO, passes the thermochemical criterion, as does a reaction involving Ca sulfate. These inferences can be generalized to atmospheres in ‘moist’ adiabatic equilibria, and to extrasolar Venus-like planets, and will help in interpreting the compositions of their atmospheres.

Several observations indicate that the cloud deck of the venusian atmosphere may provide a plausible refuge for microbial life. Having originated in a hot proto-ocean or been brought in by meteorites from Earth (or Mars), early life on Venus could have adapted to a dry, acidic atmospheric niche as the warming planet lost its oceans. The greatest obstacle for the survival of any organism in this niche may be high doses of ultraviolet (UV) radiation. Here we make the argument that such an organism may utilize sulfur allotropes present in the venusian atmosphere, particularly S(8), as a UV sunscreen, as an energy-converting pigment, or as a means for converting UV light to lower frequencies that can be used for photosynthesis. Thus, life could exist today in the clouds of Venus.

International audience; The Radiation Assessment Detector (RAD) on the Mars Science Laboratory's Curiosity rover began making detailed measurements of the cosmic ray and energetic particle radiation environment on the surface of Mars on 7 August 2012. We report and discuss measurements of the absorbed dose and dose equivalent from galactic cosmic rays and solar energetic particles on the martian surface for similar to 300 days of observations during the current solar maximum. These measurements provide insight into the radiation hazards associated with a human mission to the surface of Mars and provide an anchor point with which to model the subsurface radiation environment, with implications for microbial survival times of any possible extant or past life, as well as for the preservation of potential organic biosignatures of the ancient martian environment.

The early development of life, a fundamental question for humankind, requires the presence of a suitable planetary climate. Our understanding of how habitable planets come to be begins with the worlds closest to home. Venus, Earth, and Mars differ only modestly in their mass and distance from the Sun, yet their current climates could scarcely be more divergent. Only Earth has abundant liquid water, Venus has a runaway greenhouse, and evidence for life-supporting conditions on Mars points to a bygone era. In addition, an Earth-like hydrologic cycle has been revealed in a surprising place: Saturn's cloud-covered satellite Titan has liquid hydrocarbon rain, lakes, and river networks. Deducing the initial conditions for these diverse worlds and unravelling how and why they diverged to their current climates is a challenge at the forefront of planetary science. Through the contributions of more than sixty leading experts in the field, Comparative Climatology of Terrestrial Planets sets forth the foundations for this emerging new science and brings the reader to the forefront of our current understanding of atmospheric formation and climate evolution. Particular emphasis is given to surface-atmosphere interactions, evolving stellar flux, mantle processes, photochemistry, and interactions with the interplanetary environment, all of which influence the climatology of terrestrial planets. From this cornerstone, both current professionals and most especially new students are brought to the threshold, enabling the next generation of new advances in our own solar system and beyond.

The range of surface ages on Venus and the rate of recent volcanism are two major questions that can be addressed through an analysis of Magellan images. We report on a 3-D Monte Carlo resurfacing model that seeks to explain the resurfacing history of Venus by simulating the evolving surface under the competing processes of impact cratering and volcanism. By incorporating the observed size distribution of volcanic forms on Venus, and the assumptions of constant volcanic and impactor fluxes, we seek a solution that is consistent with the observed impact crater population. In the Monte Carlo simulations, a volcanic flux of 0.37 km3/yr, operating for 550 m.y. on initially craterless surfaces, yields surfaces that are statistically similar to Venus'. It is shown that the statistics of the impact cratering record are inconsistent with an equilibrium resurfacing model.

For hundreds of years prior to the space age, Venus was considered among the most likely homes for extraterrestrial life. Since planetary exploration began, Venus has not been considered a promising target for Astrobiological exploration. However, Venus should be central to such an exploration program for several reasons. At present Venus is the only other Earth-sized terrestrial planet that we know of, and certainly the only one we will have the opportunity to explore in the foreseeable future. Understanding the divergence of Earth and Venus is central to understanding the limits of habitability in the inner regions of habitable zones around solar-type stars. Thus Venus presents us with a unique opportunity for putting the bulk properties, evolution and ongoing geochemical processes of Earth in a wider context. Many geological and meteorological processes otherwise active only on Earth at present are currently active on Venus. Active volcanism most likely affects the climate and chemical equilibrium state of the atmosphere and surface, and maintains the global cloud cover. Further, if we think beyond the specifics of a particular chemical system required to build complexity and heredity, we can ask what general properties a planet must possess in order to be considered a possible candidate for life. The answers might include an atmosphere with signs of flagrant chemical disequilibrium and active, internally driven cycling of volatile elements between the surface, atmosphere and interior. At present, the two planets we know of which possess these characteristics are Earth and Venus. Venus almost surely once had warm, habitable oceans. The evaporation of these oceans, and subsequent escape of hydrogen, most likely resulted in an oxygenated atmosphere. The duration of this phase is poorly understood, but during this time the terrestrial planets were not isolated. Rather, due to frequent impact transport, they represented a continuous environment for early microbial life. Life, once established in the early oceans of Venus, may have migrated to the clouds which, on present day Venus, may represent a habitable niche. Though highly acidic, this aqueous environment enjoys moderate temperatures, surroundings far from chemical equilibrium, and potentially useful radiation fluxes. Observations of unusual chemistry in the clouds, and particle-populations that are not well characterized, suggest that this environment must be explored much more fully before biology can be ruled out. A sulfur-based metabolism for cloud-based life on Venus has recently been proposed (Schulze-Makuch et al., 2004). While speculative, these arguments, along with the discovery of terrestrial extremophile organisms that point toward the plausibility of survival in the Venusian clouds, establish the credibility of astrobiological exploration of Venus. Arguments for the possible existence of life on Mars or Europa are, by convention and repetition, seen as more mainstream than arguments for life elsewhere, but their logical status is similar to plausibility arguments for life on Venus. With the launch of COROT in 2006 and Kepler in 2008 the demographics of Earth-sized planets in our galaxy should finally become known. Future plans for a Terrestrial Planet Finder or Darwin-type space-based spectrograph should provide the capability of studying the atmospheric composition and other properties of terrestrial planets. One of the prime rationales for building such instruments is the possibility of identifying habitable planets or providing more generalized observational constraints on the habitable zones of stellar systems. Given the prevalence of CO 2 dominated atmospheres in our own solar system, it is quite likely that a large fraction of these will be Venus-like in composition and evolutionary history. We will be observing these planets at random times in their evolution. In analogy with our own solar system, it is just as likely that we will find representatives of early Venus and early Earth type planets from the first 2 billion years of their evolution as it is that we will find "mature Venus" and "mature Earth" type planets that are roughly 4.5 billion years old. Therefore, in order to be poised to use the results of these future observations of extrasolar planets to make valid, generalized inferences about the size, shape and evolution of stellar habitable zones it is vital that we obtain a much deeper understanding of the evolutionary histories and divergence of Earth and Venus. The Mars Exploration Rover findings of evidence for aqueous conditions on early Mars have intensified interest in the possible origin and evolution of life on early Mars. Yet the evidence suggests that these deposits were formed in a highly acidic and sulfur-rich environment. During this phase, Mars may well have had sulfuric acid clouds sustained by vigorous, sulfur-rich volcanism. This suggests that a greater understanding of the chemistry of the Venusian atmosphere and clouds, and surface/atmosphere interactions, may help to characterize the environment of Mars when life may have formed there. In turn, if signs of early life are found on Mars during the upcoming decades of intensive astrobiological exploration planned for that planet, it will strengthen arguments for the plausibility of life in an early and gradually acidifying Venusian environment. Of our two neighboring planets, Venus and Mars, it is not yet known which held on to its surface oceans, and early habitable conditions, for longer.

We report on laboratory experiments which simulate the breakdown of organic compounds under Martian surface conditions. Chambers containing Mars-analog soil mixed with the amino acid glycine were evacuated and filled to 100 mbar pressure with a Martian atmosphere gas mixture and then irradiated with a broad spectrum Xe lamp. Headspace gases were periodically withdrawn and analyzed via gas chromatography for the presence of organic gases expected to be decomposition products of the glycine. The quantum efficiency for the decomposition of glycine by light at wavelengths from 2000 to 2400 angstroms was measured to be 1.46 +/- 1.0 x 10(-6) molecules/photon. Scaled to Mars, this represents an organic destruction rate of 2.24 +/- 1.2 x 10(-4) g of C m-2 yr-1. We compare this degradation rate with the rate that organic compounds are brought to Mars as a result of meteoritic infall to show that organic compounds are destroyed on Mars at rates far exceeding the rate that they are deposited by meteorites. Thus the fact that no organic compounds were found on Mars by the Viking Lander Gas Chromatograph Mass Spectrometer experiment can be explained without invoking the presence of strong oxidants in the surface soils. The organic destruction rate may be considered as an upper bound for the globally averaged biomass production rate of extant organisms at the surface of Mars. This upper bound is comparable to the slow growing cryptoendolithic microbial communities found in dry Antarctica deserts. Finally, comparing these organic destruction rates to recently reported experiments on the stability of carbonate on the surface of Mars, we find that organic compounds may currently be more stable than calcite.

Information is pouring in about Mars. These are thrilling times for those who are proposing — and challenging — ideas about the chemical evolution of the planet and its potential for having harboured life.

The Viking Gas Chromatograph Mass Spectrometer failed to detect organic compounds on Mars, and both the Viking Labeled Release and the Viking Gas Exchange experiments indicated a reactive soil surface. These results have led to the widespread belief that there are oxidants in the martian soil. Since H2O2 is produced by photochemical processes in the atmosphere of Mars, and has been shown in the laboratory to reproduce closely the Viking LR results, it is a likely candidate for a martian soil oxidant. Here, we report on the results of a coupled soil/atmosphere transport model for H2O2 on Mars. Upon diffusing into the soil, its concentration is determined by the extent to which it is adsorbed and by the rate at which it is catalytically destroyed. An analytical model for calculating the distribution of H2O2 in the martian atmosphere and soil is developed. The concentration of H2O2 in the soil is shown to go to zero at a finite depth, a consequence of the nonlinear soil diffusion equation. The model is parameterized in terms of an unknown quantity, the lifetime of H2O2 against heterogeneous catalytic destruction in the soil. Calculated concentrations are compared with a H2O2 concentration of 30 nmoles/cm3, inferred from the Viking Labeled Release experiment. A significant result of this model is that for a wide range of H2O2 lifetimes (up to 10(5) years), the extinction depth was found to be less than 3 m. The maximum possible concentration in the top 4 cm is calculated to be approximately 240 nmoles/cm3, achieved with lifetimes of greater than 1000 years. Concentrations higher than 30 nmoles/cm3 require lifetimes of greater than 4.3 terrestrial years. For a wide range of H2O2 lifetimes, it was found that the atmospheric concentration is only weakly coupled with soil loss processes. Losses to the soil become significant only when lifetimes are less than a few hours. If there are depths below which H2O2 is not transported, it is plausible that organic compounds, protected from an oxidizing environment, may still exist. They would have been deposited by meteors, or be the organic remains of past life.