Biological and granulometric controls on sedimentary organic matter of an intertidal mudflat

A variety of measures of organic matter concentration and quality were made on samples collected from the top few mm of intertidal mudflat sediment over the course of a year, in order to assess the relative importance of biological and sedimentological influences on sedimentary organic matter. Winter and summer were times of relatively fine-grained sediment accumulation, caused by biological deposition or stabilization processes and resulting in higher organic matter concentrations. Stable carbon isotope and Br:C ratios indicated a planktonic source of bulk organic matter. Ratios of organic carbon to specific surface area of the sediments were consistent with an organic monolayer coverage of sediment grains. Correction for changing grain size during the year showed no change in the organic concentration per unit surface area, in spite of organic matter inputs by in situ primary production, buildup of heterotroph biomass and mucus coatings, and biodeposition of organic-rich seston. There were also no indications of changes in bulk organic quality, measured as hydrolyzable carbohydrates and amino acids, in response to these biological processes. It is concluded that biological processes on a seasonal time scale affect the bulk organic matter of these sediments via a modulation of grain size rather than creation or decay of organic matter.     

Amino acid analyses of Antarctic CM2 meteorites using liquid chromatography‐time of flight‐mass spectrometry

Abstract— Amino acid analyses of the Antarctic CM2 chondrites Allan Hills (ALH) 83100 and Lewis Cliff (LEW) 90500 using liquid chromatography‐time of flight‐mass spectrometry (LC‐ToF‐MS) coupled with UV fluorescence detection revealed that these carbonaceous meteorites contain a suite of indigenous amino acids not present in Antarctic ice. Several amino acids were detected in ALH 83100, including glycine, alanine, β‐alanine, γ‐amino‐n‐butyric acid (γ‐ABA), and α‐aminoisobutyric acid (AIB) with concentrations ranging from 250 to 340 parts per billion (ppb). In contrast to ALH 83100, the CM2 meteorites LEW 90500 and Murchison had a much higher total abundance of these amino acids (440–3200 ppb). In addition, ALH 83100 was found to have lower abundances of the α‐dialkyl amino acids AIB and isovaline than LEW 90500 and Murchison. There are three possible explanations for the depleted amino acid content in ALH 83100: 1) amino acid leaching from ALH 83100 during exposure to Antarctic ice meltwater, 2) a higher degree of aqueous alteration on the ALH 83100 parent body, or 3) ALH 83100 originated on a chemically distinct parent body from the other two CM2 meteorites. The high relative abundance of ?‐amino‐n‐caproic acid (EACA) in the ALH 83100 meteorite as well as the Antarctic ice indicates that Nylon‐6 contamination from the Antarctic sample storage bags may have occurred during collection.     

Outflow channel sources, reactivation, and chaos formation, Xanthe Terra, Mars

The undulating, warped, and densely fractured surfaces of highland regions east of Valles Marineris (located north of the eastern Aureum Chaos, east of the Hydraotes Chaos, and south of the Hydaspis Chaos) resulted from extensional surface warping related to ground subsidence, caused when pressurized water confined in subterranean caverns was released to the surface. Water emanations formed crater lakes and resulted in channeling episodes involved in the excavation of Ares, Tiu, and Simud Valles of the eastern part of the circum-Chryse outflow channel system. Progressive surface subsidence and associated reduction of the subsurface cavernous volume, and/or episodes of magmatic-driven activity, led to increases of the hydrostatic pressure, resulting in reactivation of both catastrophic and non-catastrophic outflow activity. Ancient cratered highland and basin materials that underwent large-scale subsidence grade into densely fractured terrains. Collapse of rock materials in these regions resulted in the formation of chaotic terrains, which occur in and near the headwaters of the eastern circum-Chryse outflow channels. The deepest chaotic terrain in the Hydaspis Chaos region resulted from the collapse of pre-existing outflow channel floors. The release of volatiles and related collapse may have included water emanations not necessarily linked to catastrophic outflow. Basal warming related to dike intrusions, thermokarst activity involving wet sediments and/or dissected ice-enriched country rock, permafrost exposed to the atmosphere by extensional tectonism and channel incision, and/or the injection of water into porous floor material, may have enhanced outflow channel floor instability and subsequent collapse. In addition to the possible genetic linkage to outflow channel development dating back to at least the Late Noachian, clear disruption of impact craters with pristine ejecta blankets and rims, as well as preservation of fine tectonic fabrics, suggest that plateau subsidence and chaos formation may have continued well into the Amazonian Period. The geologic and paleohydrologic histories presented here have important implications, as new mechanisms for outflow channel formation and other fluvial activity are described, and new reactivation mechanisms are proposed for the origin of chaotic terrain as contributors to flooding. Detailed geomorphic analysis indicates that subterranean caverns may have been exposed during chaos formation, and thus chaotic terrains mark prime locations for future geologic, hydrologic, and possible astrobiologic exploration.     

Planetary atmosphere evolution:Do other habitable planets exist and can we detect them?

The goal of this conference is to consider whether it is possible within the next few decades to detect Earth-like planets around other stars using telescopes or interferometers on the ground or in space. Implicit in the term “Earth-like” is the idea that such planets might be habitable by Earth-like organisms, or that they might actually be inhabited. Here, I shall address two questions from the standpoint of planetary atmosphere evolution. First, what are the chances that habitable planets exist around other stars? And, second, if inhabited planets exist, what would be the best way to detect them?     

Damage due to ultraviolet and ionizing radiation during the ejection of shielded micro-organisms from the vicinity of 1M ⊙ main sequence and red giant stars

We present the astrophysical conditions necessary for the ejection of shielded microorganisms from a solar system and the biological conditions involving ultraviolet and ionizing radiations to which they are subjected in space. The radiation dose for both UV and ionizing radiation from the host star, the destination star and interstellar space is calculated for three different micro-organisms. The time of transport and the survival of the micro-organisms are strongly dependent on the composition and thickness of any mantle encasing the micro-organism and on the mass/luminosity ratio of the two stars. The maximum size of grains that can be ejected from the vicinity of one solar mass main sequence and red giant stars ranges from 0.65-0.35µm and 2.1-1.2µm respectively, for a reasonable range of densities. We conclude that unshielded known micro-organisms are immediately killed by ultraviolet radiation, and that an ice mantle does not provide sufficient shielding for either type of star. However, micro-organisms shielded by a carbonaceous thin-film mantle can be ejected from the vicinity of a one solar-mass red-giant star, and such micro-organisms have a high probability of surviving damage from the ultraviolet and ionizing radiations to which they are exposed.     

Analysis of mapping coverage obtained from spacecraft

An exact analysis of the coverage obtained by spacecraft using cross-track scanning and nadir-centered conical imaging, under imposed viewing obliqueness and resolution requirements, is presented. In addition to exact expressions for the area acquired and the area acquisition rate, envelope theory is introduced to obtain the boundary of the imaged area. These expressions are relatively compact, allowing rapid machine computation. The effects of the sun phase angle, and of imaging system limitations are also examined. The Galileo mission encounter with Callisto is used as a numerical example, from which certain general conclusions are drawn regarding optimal imaging trajectories.