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94 records · Page 6Linked to original sources

USGS2018

Environmental controls, emergent scaling, and predictions of greenhouse gas (GHG) fluxes in coastal salt marshes

Coastal salt marshes play an important role in mitigating global warming by removing atmospheric carbon at a high rate. We investigated the environmental controls and emergent scaling of major greenhouse gas (GHG) fluxes such as carbon dioxide (CO 2 ) and methane (CH 4 ) in coastal salt marshes by conducting data analytics and empirical modeling. The underlying hypothesis is that the salt marsh GHG fluxes follow emergent scaling relationships with their environmental drivers, leading to parsimonious predictive models. CO 2 and CH 4 fluxes, photosynthetically active radiation (PAR), air and soil temperatures, well water level, soil moisture, and porewater pH and salinity were measured during May–October 2013 from four marshes in Waquoit Bay and adjacent estuaries, MA, USA. The salt marshes exhibited high CO 2 uptake and low CH 4 emission, which did not significantly vary with the nitrogen loading gradient (5–126 kg · ha −1 · year −1 ) among the salt marshes. Soil temperature was the strongest driver of both fluxes, representing 2 and 4–5 times higher influence than PAR and salinity, respectively. Well water level, soil moisture, and pH did not have a predictive control on the GHG fluxes, although both fluxes were significantly higher during high tides than low tides. The results were leveraged to develop emergent power law‐based parsimonious scaling models to accurately predict the salt marsh GHG fluxes from PAR, soil temperature, and salinity (Nash‐Sutcliffe Efficiency = 0.80–0.91). The scaling models are available as a user‐friendly Excel spreadsheet named Coastal Wetland GHG Model to explore scenarios of GHG fluxes in tidal marshes under a changing climate and environment.

Massachusetts↗

USGS2010

Detection and mapping of hydrocarbon deposits on Titan

We report the identification of compounds on Titan's surface by spatially resolved imaging spectroscopy methods through Titan's atmosphere, and set upper limits to other organic compounds. We present evidence for surface deposits of solid benzene (C 6 H 6 ), solid and/or liquid ethane (C 2 H 6 ), or methane (CH 4 ), and clouds of hydrogen cyanide (HCN) aerosols using diagnostic spectral features in data from the Cassini Visual and Infrared Mapping Spectrometer (VIMS). Cyanoacetylene (2-propynenitrile, IUPAC nomenclature, HC 3 N) is indicated in spectra of some bright regions, but the spectral resolution of VIMS is insufficient to make a unique identification although it is a closer match to the feature previously attributed to CO 2 . We identify benzene, an aromatic hydrocarbon, in larger abundances than expected by some models. Acetylene (C 2 H 2 ), expected to be more abundant on Titan according to some models than benzene, is not detected. Solid acetonitrile (CH 3 CN) or other nitriles might be candidates for matching other spectral features in some Titan spectra. An as yet unidentified absorption at 5.01- μ m indicates that yet another compound exists on Titan's surface. We place upper limits for liquid methane and ethane in some locations on Titan and find local areas consistent with millimeter path lengths. Except for potential lakes in the southern and northern polar regions, most of Titan appears “dry.” Finally, we find there is little evidence for exposed water ice on the surface. Water ice, if present, must be covered with organic compounds to the depth probed by 1–5- μ m photons: a few millimeters to centimeters.

Journal of Geophysical Research - Planets↗

USGS2000

Identification of a basaltic component on the Martian surface from Thermal Emission Spectrometer data

The Mars Global Surveyor Thermal Emission Spectrometer (TES) instrument collected 4.8×10 6 spectra of Mars during the initial aerobraking and science‐phasing periods of the mission (September 14, 1997, through April 29, 1998). Two previously developed atmosphere‐removal models were applied to data from Cimmeria Terra (25°S, 213°W). The surface spectra derived for these two models agree well, indicating that the surface and atmosphere emission can be separated and that the exact atmosphere‐removal model used has little effect on the derived surface composition. The Cimmeria spectra do not match terrestrial high‐silica igneous rocks (granite and rhyolite), ultramafic igneous rocks, limestone, or quartz‐ and clay‐rich sandstone and siltstone. A particulate (sand‐sized) sample of terrestrial flood basalt does provide an excellent match in both spectral shape and band depth to the Cimmeria spectrum over the entire TES spectral range. No unusual particle size effects are required to account for the observed spectral shape and depth. The implied grain size is consistent with the thermal inertia and albedo of this region, which indicate a sand‐sized surface with little dust. The identification of basalt is consistent with previous indications of pyroxene and basalt‐like compositions from visible/near‐infrared and thermal‐infrared spectral measurements. A linear spectral deconvolution model was applied to both surface‐only Cimmeria spectra using a library of 60 minerals to determine the composition and abundance of the component minerals. Plagioclase feldspar (45%; 53%) and clinopyroxene (26%; 19%) were positively identified above an estimated detection threshold of 10–15% for these minerals. The TES observations provide the first identification of feldspars on Mars. The best fit to the Mars data includes only clinopyroxene compositions; no orthopyroxene compositions are required to match the Cimmeria spectra. Olivine (12%; 12%) and sheet silicate (15%; 11%) were identified with lower confidence. Carbonates, quartz, and sulfates were not identified in Cimmeria at detection limits of ∼5, 5, and 10%, respectively. Their presence elsewhere, however, remains open. The Cimmeria spectra are not well matched by any one SNC meteorite spectrum, indicating that this region is not characterized by a single SNC lithology. The occurrence of unweathered feldspar and pyroxene in Cimmeria, together with the inferred presence of pyroxene and unweathered basalts in other dark regions and at the Viking and Pathfinder landing sites, provides evidence that extensive global chemical weathering of materials currently exposed on the Martian surface has not occurred.

Journal of Geophysical Research: Planets↗

USGS2000

Detection of crystalline hematite mineralization on Mars by the Thermal Emission Spectrometer: evidence for near-surface water

The Thermal Emission Spectrometer (TES) instrument on the Mars Global Surveyor (MGS) mission has discovered a remarkable accumulation of crystalline hematite (α-Fe 2 O 3 ) that covers an area with very sharp boundaries approximately 350 by 350–750 km in size centered near 2°S latitude between 0° and 5°W longitude (Sinus Meridiani). Crystalline hematite is uniquely identified by the presence of fundamental vibrational absorption features centered near 300, 450, and >525 cm −1 and by the absence of silicate fundamentals in the 1000 cm −1 region. Spectral features resulting from atmospheric CO 2 , dust, and water ice were removed using a radiative transfer model. The spectral properties unique to Sinus Meridiani were emphasized by removing the average spectrum of the surrounding region. The depth and shape of the hematite fundamental bands show that the hematite is crystalline and relatively coarse grained (>5–10 μm). Diameters up to and greater than hundreds of micrometers are permitted within the instrumental noise and natural variability of hematite spectra. Hematite particles <5–10 μm in diameter (as either unpacked or hard-packed powders) fail to match the TES spectra. The spectrally derived areal abundance of hematite varies with particle size from ∼10% (>30 μm diameter) to 40–60% (10 μm diameter). The hematite in Sinus Meridiani is thus distinct from the fine-grained (diameter <5–10 μm), red, crystalline hematite considered, on the basis of visible, near-IR data, to be a minor spectral component in Martian bright regions like Olympus-Amazonis. Sinus Meridiani hematite is closely associated with a smooth, layered, friable surface that is interpreted to be sedimentary in origin. This material may be the uppermost surface in the region, indicating that it might be a late stage sedimentary unit or a layered portion of the heavily cratered plains units. We consider five possible mechanisms for the formation of coarse-grained, crystalline hematite. These processes fall into two classes depending on whether they require a significant amount of near-surface water: the first is chemical precipitation that includes origin by (1) precipitation from standing, oxygenated, Fe-rich water (oxide iron formations), (2) precipitation from Fe-rich hydrothermal fluids, (3) low-temperature dissolution and precipitation through mobile ground water leaching, and (4) formation of surface coatings, and the second is thermal oxidation of magnetite-rich lavas. Weathering and alteration processes, which produce nanophase and red hematite, are not consistent with the coarse, crystalline hematite observed in Sinus Meridiani. We prefer chemical precipitation models and favor precipitation from Fe-rich water on the basis of the probable association with sedimentary materials, large geographic size, distance from a regional heat source, and lack of evidence for extensive groundwater processes elsewhere on Mars. The TES results thus provide mineralogic evidence for probable large-scale water interactions. The Sinus Meridiani region may be an ideal candidate for future landed missions searching for biotic and prebiotic environments, and the physical characteristics of this site satisfy all of the engineering requirements for the missions currently planned.

Journal of Geophysical Research E: Planets↗