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[The role of biosphere in the formation of the Earth climate. A greenhouse catastrophe].

The role of processes in organic and inorganic nature that determine the formation of the atmosphere chemical composition and Earth temperature balance was analyzed. It was concluded that the biological mechanisms of CO2 removal from the atmosphere are insufficient, and there exist potentially hazardous CO2 sources in inorganic nature that can be activated upon elevation of the mean Earth temperature. It was shown that the stability of natural systems of maintaining the constant chemical composition of the atmosphere is destroyed due to the disturbance by man of climate-forming biocenoses, which may lead to irreversible changes in Earth's climate with the result that the mean planetary temperature would be elevated to 100-150 degrees C and above. This would make impossible the existence of life on our planet, at least in its present form. A radiation-adiabatic model of the greenhouse effect was constructed in the framework of which asymptotic estimates of the increase in mean planet temperatures for a wide range of changes in the concentration of greenhouse gases were obtained. On the basis of the model, an integral model of changes in Earth's climate was constructed, which takes into account the heat inertia of the ocean and aerosol contaminations of the upper layers of the atmosphere. It was shown that irreversible (catastrophic) changes in Earth's climate (greenhouse catastrophe) may occur in a relatively near future (200-300 years).

Algorithms↗

Exobiology: a critical review.

The quest for life beyond the Earth can be implemented in three ways. First, we may study contemporary terrestrial biology and organic chemistry to approach the problem of the origin of life on Earth. If it appears relatively easy for life to have emerged in the primitive terrestrial environment, it may follow that the origin of life is a fairly general planetary phenomenon. Second, we can investigate the physical environments of the planets, and determine whether the conditions there are so severe that living processes are entirely excluded, even allowing for the adaptability of life. Third, the planets may be studied for direct evidence of indigenous life forms. All three approaches are beset with uncertainties, and it is important to state at the outset that no completely convincing evidence exists for extraterrestrial life. The problem often reduces to probability considerations, and to estimates of observational reliability. At convenient places in the marshalling of evidence, I shall try to pause and give brief expression to alternative interpretations. In almost all cases, an optimistic view can be found which holds that the evidence is strongly suggestive of, or at the worst, not inconsistent with, the existence of extraterrestrial life; and a pessimistic view can be found, which holds that the evidence adduced in favor of extraterrestrial life is unconvincing, irrelevant, or has an alternative, non-biological explanation. I leave it to the reader to pick his own way among the factions.

Atmosphere↗

New statements on the Gaia theory.

Gaia is the name the ancient Greeks gave to their goddess of the Earth and is the root of words like geography and geology. Gaia is also a straightforward scientific theory about the Earth and the organisms that inhabit it. Gaia theory is testable and has a proper mathematical basis in a set of closely coupled differential equations. We do not yet know if it is a good explanation of the way our planet works; the evidence is only partially gathered. Its main value at this stage is to provide a different way to look at the Earth. In science, Gaia theory has already led to significant discoveries but just as important it forces us to question whether the good of humankind is the only thing that matters. The true value of the journeys into space was to reveal the Earth as a live planet. They made us realise for the first time that humanism is not enough. The view from space teaches that we are part of a greater entity, the Earth, and that our survival and its good health are inextricably entwined. Perhaps in time we can expand our view to encompass the larger systems of the galaxy and the Universe. Now the Earth needs our full attention.

Earth, Planet↗

Genomic potential hypothesis of evolution: a concept of biogenesis in habitable spaces of the universe.

The new hypothesis of evolution establishes a contiguity of life sciences with cosmology, physics, and chemistry, and provides a basis for the search for life on other planets. Chemistry is the sole driving force of the assembly of life, under the subtle guidance exerted by bonding orbital geometry. That phenomenon leads to multiple origins that function on the same principles but are different to the extent that their nucleic acid core varies. Thus, thoughts about the origins of life and the development of complexity have been transferred from the chance orientation of the past to the realm of atomic structures, which are subject to the laws of thermodynamics and kinetics. Evolution is a legitimate subject of basic science, and the complexity of life will submit to the laws of chemistry and physics as the problem is viewed from a new perspective. The paradigm connects life to the big events that formed every sphere of our living space and that keeps conditions fine-tuned for life to persist, perhaps a billion years or more. The "genomic potential" hypothesis leads to the prediction that life like ours is likely to exist in galaxies that are as distant from the origin of the universe as the Milky Way, and that the habitable zone of our galaxy harbors other living planets as well.

Biological Evolution↗

Cometary deuterium.

Deuterium fractionations in cometary ices provide important clues to the origin and evolution of comets. Mass spectrometers aboard spaceprobe Giotto revealed the first accurate D/H ratios in the water of Comet 1P/Halley. Ground-based observations of HDO in Comets C/1996 B2 (Hyakutake) and C/1995 O1 (Hale-Bopp), the detection of DCN in Comet Hale-Bopp, and upper limits for several other D-bearing molecules complement our limited sample of D/H measurements. On the basis of this data set all Oort cloud comets seem to exhibit a similar (D/H)H2O ratio in H2O, enriched by about a factor of two relative to terrestrial water and approximately one order of magnitude relative to the protosolar value. Oort cloud comets, and by inference also classical short-period comets derived from the Kuiper Belt cannot be the only source for the Earth's oceans. The cometary O/C ratio and dynamical reasons make it difficult to defend an early influx of icy planetesimals from the Jupiter zone to the early Earth. D/H measurements of OH groups in phyllosilicate rich meteorites suggest a mixture of cometary water and water adsorbed from the nebula by the rocky grains that formed the bulk of the Earth may be responsible for the terrestrial D/H. The D/H ratio in cometary HCN is 7 times higher than the value in cometary H2O. Species-dependent D-fractionations occur at low temperatures and low gas densities via ion-molecule or grain-surface reactions and cannot be explained by a pure solar nebula chemistry. It is plausible that cometary volatiles preserved the interstellar D fractionation. The observed D abundances set a lower limit to the formation temperature of (30 +/- 10) K. Similar numbers can he derived from the ortho-to-para ratio in cometary water, from the absence of neon in cometary ices and the presence of S2. Noble gases on Earth and Mars, and the relative abundance of cometary hydrocarbons place the comet formation temperature near 50 K. So far all cometary D/H measurements refer to bulk compositions, and it is conceivable that significant departures from the mean value could occur at the grain-size level. Strong isotope effects as a result of coma chemistry can be excluded for molecules H2O and HCN. A comparison of the cometary (D/H)H2O ratio with values found in the atmospheres of the outer planets is consistent with the long-held idea that the gas planets formed around icy cores with a high cometary D/H ratio and subsequently accumulated significant amounts of H2 from the solar nebula with a low protosolar D/H.

Deuterium↗

Molten earth and the origin of prebiological molecules.

Evidence for the molten Earth at its accretion time has been accumulated through the geochemical investigations and the observations of the surfaces of planets by space probes such as Venera 8, Mariner 9, Surveyor, Luna, and Apollo. The primitive terrestrial atmosphere might have been derived from the volcanic gases, as suggested by Rubey, but of a higher temperature than so far assumed. A thermochemical calculation of the composition of the volcanic gas suggests the following possibilities: (1) Large amounts of H2 and CO were present in the primitive atmosphere. This gives a theoretical basis for the HCN-production experiment by Abelson. (2) HCHO and NH3 existed in the primitive oceans, of the amount comparable with the weight of the present biosphere. (3) Plenty of NO3-, SO4, and PO4 were expected in the primitive oceans. The NO3- ions might have been useful for the nitrate respiration advocated by Egami. In an appendix, it is argued, on ;he basis of the observational evidence of the exospheric temperatures of planets by space probes, that a highly reducing atmosphere would (if it existed on the primitive Earth) have disappeared very quickly due to the thermal escape of hydrogen from its exosphere.

Atmosphere↗

The Viking Mission: implications for life on Mars.

The results of the Viking Biology experiments are best explained by non-biological phenomena: The interaction of the reagents with the materials comprising the regolith. Conditions of water activity, temperature, availability of carbon sources and others in most regions of the planet are too extreme for survival and growth of any known Earth microorganisms. Although the possibility persists that some very unusual form of life is somewhere on that planet the evidence is best interpreted as negative. Even though there is no evidence for current life on Mars, whether or not life ever originated there is not known.

Carbon↗

Arthropods and Multispecies Habitat Conservation Plans: Are We Missing Something?

Arthropods constitute well over one-half of the species of higher life on the planet and are the dominant terrestrial life form on the planet. Unfortunately, very little is known about most arthropod species. There are an estimated 163,487 species of insects in North America, of which only 66% are taxonomically known. Similarly, there are an estimated 35,514 species of North American arachnids, of which only 9316 are described; over 73% have yet to be discovered and described. Without the basic taxonomic and life history knowledge for most of the terrestrial species (i.e., arthropods) of North American ecosystems, land managers are faced with the challenge of developing, selecting, and managing biotic reserves and habitat conservation plans for which they know very little about the majority of organisms found within such reserves or covered by such plans. With respect to arthropods, this challenge includes taking into account poorly described species being used as political tools to stop development (as opposed to actually protecting a truly endangered species), thus confounding the habitat conservation planning process and ensuring that "surprises" in the form of new listings will occur within any multispecies habitat plan. Finally, using various scenarios and assumptions, estimates of the true number of endangered insects and arachnids are provided to illustrate the fact that the suspected number of threatened, endangered, and extinct species is probably low by at least an order of magnitude.

Journal Article↗

Studies of biominerals relevant to the search for life on Mars.

The evidence of the water erosion on Mars is particularly interesting since present climatic conditions are such that liquid water cannot exist at the surface. But, if water was present on the planet in the past, there may have been life, too. Since the discovery of carbonates on Mars also may have very important implications on the possibility that life developed there, we are studying minerals that can have biotic or abiotic origin: calcite (CaCO(3)) and aragonite, a metastable state of calcite.We have analysed biomineral aragonite, in the form of recent sea shells, as well as crystals of mineral aragonite. Infrared spectroscopy in the 2-25 mum wavelength range reveals that, after thermal processing, the biotic samples have a different spectral behaviour from the abiotic ones. As a result, it is possible to distinguish abiotic mineral aragonite from aragonite of recent biological origin.Obviously, if life existed in the past on the Red Planet, we could expect to find "ancient" biotic carbonates, which should therefore be investigated, in order to search for a way of discriminating them from abiotic minerals. For this reason, at the beginning we have considered samples of crushed fossil shells of aragonite composition. Afterwards, in order to take into account that fossilization processes almost always produce a transformation of metastable form (aragonite) into more stable form (calcite), we also studied samples of mineral calcite and different types of fossils completely transformed into calcite. All these biotic fossil samples show the same spectral behaviour as the fresh biotic material after thermal annealing at 485 degrees C. Instead, the calcite behaves like abiotic aragonite.Furthermore, it is known that seashells and other biominerals are formed through an intimate association of inorganic materials with organic macromolecules. The macromolecules control the nucleation, structure, morphology, crystal orientation and spatial confinement of the inorganic phase: this differentiates biominerals from minerals. Analysing the aragonite or calcite fossils with a Scanning Electron Microscope, we found that the fossilization process did not modify the structure of the biominerals which maintain their microscopic characteristics. Looking at the morphology of fossil biominerals, it is evident that the crystals are arranged in complex architectures compared with the compact structure of the mineral crystals. In conclusion, the properties and structure of the biominerals are different from those of the minerals. The rapid increase of the crystalline structure developed under biotic conditions makes these minerals less resistant to thermal treatments, compared with samples of abiotic origin. This result holds both for recent shells as well as all fossil samples. The spectroscopic behaviour of all analysed calcium carbonates of biotic origin is different from that of the abiotic one. Therefore, the infrared spectroscopy is a valid technique to discern the origin of the samples and a powerful tool for analysing in-situ and "sample-return" Mars missions specimens. Also Optical and Scanning Electron Microscopy can be useful to support this type of studies.

Calcium Carbonate↗

Water loss on Venus: the role of carbon monoxide.

The abundance of water on Venus is four to five orders of magnitude lower than on the Earth. This difference may reflect initial differences in the bulk volatile contents of the two planets, or may be the result of processes for massive water loss on Venus. A series of thermodynamic calculations are performed on the heterogeneous system C-O-H-N-S, varying C/H upward from its terrestrial value of 0.033 in order to evaluate the extent to which either of these two possibilities may account for the low water content on Venus. Relative abundances of 84 molecular gaseous species are computed as functions of temperature, total pressure, oxygen fugacity, and bulk C/H. As bulk C/H increases, the complement of atmospheric H2O decreases, but C/H would have to be raised to an improbably high value to account for the low water abundance on Venus by initial deficiency alone. Increasing C/H also results in a rapid increase in CO/H2O, however, and enhances water loss by the reaction CO + H2O = CO2 + H2 or by reaction of carbon monoxide with the free oxygen liberated by photodissociation of water. Other water loss mechanisms have relied on crustal FeO as an oxygen sink. Such mechanisms, however, should have operated on both Venus and the Earth and may be insufficient to account for the major differences in present H2O abundance between the two planets. Calculations performed in this study suggest that if the outgassed C/H on Venus was higher than on Earth by even less than a factor of 5, it would have been sufficient to make carbon monoxide competitive with FeO as a sink for oxygen. Together with the lower initial water abundance that follows from a higher C/H, water loss involving CO may have been a major factor in determining the present low abundance of water on Venus.

Atmosphere↗

The case for a wet, warm climate on early Mars.

Theoretical arguments are presented in support of the idea that Mars possessed a dense CO2 atmosphere and a wet, warm climate early in its history. Calculations with a one-dimensional radiative-convective climate model indicate that CO2 pressures between 1 and 5 bars would have been required to keep the surface temperature above the freezing point of water early in the planet's history. The higher value corresponds to globally and orbitally averaged conditions and a 30% reduction in solar luminosity; the lower value corresponds to conditions at the equator during perihelion at times of high orbital eccentricity and the same reduced solar luminosity. The plausibility of such a CO2 greenhouse is tested by formulating a simple model of the CO2 geochemical cycle on early Mars. By appropriately scaling the rate of silicate weathering on present Earth, we estimate a weathering time constant of the order of several times 10(7) years for early Mars. Thus, a dense atmosphere could have persisted for a geologically significant time period (approximately 10(9) years) only if atmospheric CO2 was being continuously resupplied. The most likely mechanism by which this might have been accomplished is the thermal decomposition of carbonate rocks induced directly and indirectly (through burial) by intense, global-scale volcanism. For plausible values of the early heat flux, the recycling time constant is also of the order of several times 10(7) years. The amount of CO2 dissolved in standing bodies of water was probably small; thus, the total surficial CO2 inventory required to maintain these conditions was approximately 2 to 10 bars. The amount of CO2 in Mars' atmosphere would eventually have dwindled, and the climate cooled, as the planet's internal heat engine ran down. A test for this theory will be provided by spectroscopic searches for carbonates in Mars' crust.

Atmosphere↗

Microbial metabolism of tholin.

In this paper, we show that a wide variety of common soil bacteria are able to obtain their carbon and energy needs from tholin (a class of complex organic heteropolymers thought to be widely distributed through the solar system; in this case tholin was produced by passage of electrical discharge through a mixture of methane, ammonia, and water vapor). We have isolated aerobic, anaerobic, and facultatively anaerobic bacteria which are able to use tholin as a sole carbon source. Organisms which metabolize tholin represent a variety of bacterial genera including Clostridium, Pseudomonas, Bacillus, Acinetobacter, Paracoccus, Alcaligenes, Micrococcus, Corynebacterium, Aerobacter, Arthrobacter, Flavobacterium, and Actinomyces. Aerobic tholin-using bacteria were first isolated from soils containing unusual or sparse carbon sources. Some of these organisms were found to be facultatively anaerobic. Strictly anaerobic tholin-using bacteria were isolated from both carbon-rich and carbon-poor anaerobic lake muds. In addition, both aerobic and anaerobic tholin-using bacteria were isolated from common soil collected outside the laboratory building. Some, but not all, of the strains that were able to obtain carbon from tholin were also able to obtain their nitrogen requirements from tholin. Bacteria isolated from common soils were tested for their ability to obtain carbon from the water-soluble fraction, the ethanol-soluble fraction, and the water/ethanol-insoluble fraction of the tholin. Of the 3.5 x 10(7) bacteria isolated per gram of common soils, 1.7, 0.5, and 0.2%, respectively, were able to obtain their carbon requirements from the water-soluble fraction, the ethanol-soluble fraction and the water/ethanol-insoluble fraction of the tholin. The palatability of tholins to modern microbes may have implications for the early evolution of microbial life on Earth. Tholins may have formed the base of the food chain for an early heterotrophic biosphere before the evolution of autotrophy on the early Earth. Where tholins are present on other planets, they could possibly be metabolized by contaminant microorganisms transported to these bodies via spacecraft. Thus, the presence of tholins should be taken into account when evaluating the planetary quarantine requirements for probes to other planets.

Amino Acids↗

On the possibility of chemosynthetic ecosystems in subsurface habitats on Mars.

We have reexamined the question of extant microbial life on Mars in light of the most recent information about the planet and recently discovered nonphotosynthetic microbial ecosystems on Earth--deep sea hydrothermal vent communities and deep subsurface aquifer communities. On Mars, protected subsurface niches associated with hydrothermal activity could have continued to support life even after surface conditions became inhospitable. Geochemical evidence from the SNC meteorites and geomorphological evidence for recent volcanism suggest that such habitats could persist to the present time. There are also extensive geological features that attest to the ubiquitous nature of volcano-ground ice interactions on Mars. We suggest a possible deep subsurface microbial ecology similar to those discovered to depths of several kilometers below the surface of the Earth. We focus on anaerobic systems utilizing CO2 as the primary source of carbon. Liquid water could be provided by the heat of geothermal or volcanic activity melting permafrost or other subsurface water sources. Gases from volcanic activity deep in the planet could provide reducing power (as CH4, H2, or H2S) percolating up from below and enabling the development of a microbial community based upon chemolithoautotrophy. We suggest a methanogen (or acetogen) and sulfur-based microbial ecology as one possible basis for microbial primary production. Our hypothetical ecosystem is neither supported, nor excluded, by current observations of Mars. Tests for such a subsurface system involve locating active geothermal areas associated with ground ice or detecting trace quantities of reduced atmospheric gases that would leak from such a system.

Carbon Dioxide↗

Separation and purification of peptides by high-speed counter-current chromatography.

Preparative separations of peptides have been accomplished using high-speed counter-current chromatography. This has been made possible by the use of a particular solvent system that does not exhibit solvent carryover at high speed flow and centrifugation conditions. The solvent system composed of tert.-butyl methyl ether, n-butanol, acetonitrile and aqueous trifluoroacetic acid which can be adjusted in volume ratios and percent acid is employed in two instruments for counter-current chromatography. The cross-axis coil planet centrifuge was used for separation of various dipeptides. Superior resolution was obtained with the multi-layer coil planet centrifuge in the separation of six dipeptides and in the preparative purification of two synthetic peptides.

Amino Acid Sequence↗

A study of chemical systems using signal flow graph theory: application to Neptune.

Photochemistry of giant planets and their satellites is characterized by numerous reactions involving many chemical species. In the present paper, chemical systems are modeled by signal flow graphs. Such a technique evaluates the transmission of any input into the system (solar flux, electrons...) and gives access to the identification of the most important mechanisms in the chemical system. For a given chemical system, we first evaluate rate coefficients. Then, in order to obtain concentrations of each compound, we integrate the set of continuity equations by Gear's method. Gear's method is chosen rather than another classical method because it is recommended for a system of stiff equations due to the existence of greatly differing time constants. Finally, the technique of signal flow graphs is used. This method is applied to the production of hydrocarbons in the atmospheres of giant planets. In particular, the production of C2H6 in the atmosphere of Neptune from the photodissociation of CH4 is investigated. Different paths of dissociation of CH4 are possible from L alpha radiations. A chemical system containing 14 species and 30 reactions including these different paths of dissociation is integrated. The main mechanism of production of C2H6 is identified and evaluated for each model of dissociation. The importance of various reaction paths as a function of time is discussed.

Atmosphere↗

Oxygenic photosynthesis and the oxidation state of Mars.

The oxidation state of the Earth's surface is one of the most obvious indications of the effect of life on this planet. The surface of Mars is highly oxidized, as evidenced by its red color, but the connection to life is less apparent. Two possibilities can be considered. First, the oxidant may be photochemically produced in the atmosphere. In this case the fundamental source of O2 is the loss of H2 to space and the oxidant produced is H2O2. This oxidant would accumulate on the surface and thereby destroy any organic material and other reductants to some depth. Recent models suggest that diffusion limits this depth to a few meters. An alternative source of oxgyen is biological oxygen production followed by sequestration of organic material in sediments--as on the Earth. In this case, the net oxidation of the surface was determined billions of years ago when Mars was a more habitable planet and oxidative conditions could persist to great depths, over 100 m. Below this must be a compensating layer of biogenic organic material. Insight into the nature of past sources of oxidation on Mars will require searching for organics in the Martian subsurface and sediments.

Atmosphere↗

Review of methodology and technology available for the detection of extrasolar planetary systems.

Anyone undertaking an interstellar voyage might wish to be assured of the existence of a safe planetary harbor at the other end! Aside from the obvious interest of the participants in this Symposium, astronomers and astrophysicists are also eager to detect and study other planetary systems in order to better understand the formation of our own Solar System. Scientists involved in the search for extraterrestrial intelligence argue that planets suitable for the evolution of life may abound elsewhere within our own Milky Way Galaxy. On theoretical grounds, they are probably correct, but they lack any observational support. For in spite of decades of claimed astrometric detections of planetary companions and the recent exciting and tantalizing observations from the IRAS satellite and the IR speckle observations of Van Biesbroeck 8 and other cool stars, there is no unambiguous proof for the existence of another planetary system beyond our own. In this paper we review the various methods for detecting extrasolar planets and briefly describe the Earth and space based technology currently available and discuss the near-term plans to implement these different search techniques. In each case an attempt is made to identify the limiting source of systematic error inherent to the methodology and to assess the potential for technological improvements.

Astronomical Phenomena↗

Biological nitrogen fixation under primordial Martian partial pressures of dinitrogen.

Early Earth and early Mars were similar enough such that past geochemical and climatic conditions on Mars may have also been favorable for the origin of life. However, one of the most striking differences between the two planets was the low partial pressure of dinitrogen (pN2) on early Mars (18 mb). On Earth, nitrogen is a key biological element and in many ecosystems the low availability of fixed nitrogen compounds is the main factor limiting growth. Biological fixation of dinitrogen on Earth is a crucial source of fixed nitrogen. Could the low availability of dinitrogen in the primordial Martian atmosphere have prevented the existence, or evolution of Martian microbiota? Azotobacter vinelandii and Azomonas agilis were grown in nitrogen free synthetic medium under various partial pressures of dinitrogen ranging from 780-0 mb (total atmosphere=1 bar). Below 400 mb the biomass, cell number, and growth rate decreased with decreasing pN2. Both microorganisms were capable of growth at a pN2 as low as 5 mb, but no growth was observed at a pN2 < or = 1 mb. The data appear to indicate that biological nitrogen fixation could have occurred on primordial Mars (pN2=18 mb) making it possible for a biotic system to have played a role in the Martian nitrogen cycle. It is possible that nitrogen may have played a key role in the early evolution of life on Mars, and that later a lack of available nitrogen on that planet (currently, pN2=0.2 mb) may have been involved in its subsequent extinction.

Atmosphere↗