Characterization of dissolved organic matter fluorescence in the South Atlantic Bight with use of PARAFAC model: Interannual variability

Systematic water sampling for characterization of chromophoric dissolved organic matter (CDOM) in the coastal South Atlantic Bight, was conducted as part of the long term Coastal Ocean Research and Monitoring Program (CORMP). Water samples were collected during a 3.5 year period, from October 2001 until March 2005, in the vicinity of the Cape Fear River (CFR) outlet and in adjacent Onslow Bay (OB). During this study there were two divergent hydrological and meteorological conditions in the CFR drainage area: a severe drought in 2002, followed by the very wet year of 2003. CDOM was characterized optically by the absorption coefficient at 350 nm, the spectral slope coefficient (S), and by Excitation Emission Matrix (EEM) fluorescence. Parallel Factor Analysis (PARAFAC) was used to assess CDOM composition from EEM spectra and six components were identified: three terrestrial humic-like components, one marine humic-like component and two protein-like components. Terrestrial humic-like components contributed most to dissolved organic matter (DOM) fluorescence in the low salinity plume of the CFR. The contribution of terrestrial humic-like components to DOM fluorescence in OB was much smaller than in the CFR plume area. Protein-like components contributed significantly to DOM fluorescence in the coastal ocean of OB and they dominated DOM fluorescence in the Gulf Stream waters. Hydrological conditions during the observation period significantly impacted both concentration and composition of CDOM found in the estuary and coastal ocean. In the CFR plume, there was an order of magnitude difference in CDOM absorption and fluorescence intensity between samples collected during the drought compared to the wet period. During the drought, CDOM in the CFR plume was composed of equal proportions of terrestrial humic-like components (ca. 60% of the total fluorescence intensity) with a significant contribution of proteinaceous substances (ca. 20% of the total fluorescence). During high river flow, CDOM was composed mostly of humic substances (nearly 75% of total fluorescence) with minor contributions by proteinaceous substances. The impact of changes in fresh water discharge patterns on CDOM concentration and composition was also observed in OB, though to a lesser degree.     

Long-term ecosystem and biogeochemical research in Loch Vale watershed,Rocky Mountain National Park,Colorado

Loch Vale watershed was instrumented in 1983 with initial support from the National Acid Precipitation Assessment Program to ask whether ecosystems of Rocky Mountain National Park (RMNP) were affected by acidic atmospheric deposition. Research and monitoring activities were expanded in 1991 by the U.S. Geological Survey Water, Energy, and Biogeochemical Budgets program to understand the processes, and their interactions, controlling water, energy, and biogeochemical fluxes. With help from many collaborators we have characterized trends and patterns in atmospheric deposition, climate, and hydrology, including glaciers and other ice features. Instead of acidic deposition, we documented high atmospheric inputs of reactive nitrogen (Nr), and have studied the ecological consequences in soils, surface water, and vegetation. Using paleolimnology, we documented the onset of human-caused change to lake primary producers ca. 1950 in response to increased Nr deposition and warming. Our results provided the basis for the Colorado Nitrogen Deposition Reduction Plan, a state policy that aims to reduce Nr emissions to protect resources in RMNP by 2032. Carbon cycle research revealed mountain wetlands now release more carbon than they store, and respiration and methane flux occurs even during winter through deep snow packs. Trend analyses found export of Nr to be closely tied to atmospheric inputs, but can lag in response to drought. Current research explores consequences of the combination of warming, changes in precipitation dynamics, and atmospheric deposition of Nr and dust on stream and lake CO₂ dynamics, lake biology and trophic state, and soil carbon composition. Dramatic increases in park visitors have prompted studies on the effects of recreational use on water quality. New tools such as remote sensing and high frequency instream water quality sensors are being applied to lake and stream studies. Monitoring, combined with experiments, models, and spatial comparisons is an essential foundation for science-based resource management.     

Computational models of community resilience

Natural Hazards - Protecting civil infrastructure from natural and man-made hazards is vital. Understanding the impact of these hazards helps allocate resources efficiently. Researchers have...     

Geochemical evidence of microbial activity within ooids

Ooid formation remains elusive despite their importance as palaeoclimatic indicators and important contributors to global carbonate budget. Based on stable isotopes, nutrient and elemental analyses on solid components and ooidal leachates, this study supports the notion of microbial involvement in the development of ooids from Great Bahama Bank. Carbon and nitrogen isotopic analyses on organic fractions identified geochemical signatures of microbial activity. The δ¹³C values for organic carbon in the bulk (?11·9 to ?16·9‰); intercrystalline/intracrystalline (?11·9 to 16·7‰); and intracrystalline phases (?12·4 to ?17·7‰) were similar and, except for the more enriched values of ooids from Butterfly Beach, were within the range of photosynthesisers. The δ¹⁵N values for the bulk (+0·5 to ?0·2‰); intercrystalline/intracrystalline (?0·3‰ to ?0·7‰) and intracrystalline organic matter (?0·3 to ?1·7‰) showed a narrow range consistent with nitrogen fixation. While positive δ¹⁵N and δ¹⁸O values of the leached from the ooids provided evidence of denitrification, the carbonate associated sulphate δ³⁴S_CAS of the bulk sediments (+19·2 to +19·6‰) and δ³⁴S of the leachates (+16·6 to +18·3‰) provided weak indication of sulphate reduction, suggesting either that high concentrations of isotopically enriched S are overriding bio‐signatures of sulphate reduction or that microbes are preferentially using as an electron acceptor. In contrast, the elevated sulphate concentrations of the leachates suggest the occurrence of microbial sulphide oxidation within ooids. The high Mg/Ca of the leachates and scanning electron microscope analyses provide putative evidence of amorphous calcium carbonate and a formative role in CaCO₃ precipitation. Together, these findings indicate that a redox dependent microbial consortium may influence CaCO₃ precipitation in the form of ooid accretion, cementation and micritization. It is also inferred that ooid deposits are not suitable indicators of palaeoclimate because ooids are affected throughout their life by a complex chain of abiotic and biological processes which can lead to large geochemical offsets.     

Low stable carbon isotope fractionation by coccolithophore RubisCO

The ¹³C/¹²C ratio of carbon compounds is used to identify sources and sinks in the global carbon cycle. However, the relatively enriched ¹³C content observed for marine organic carbon remains enigmatic. The majority of oceanic carbon is fixed by algae and cyanobacteria via the Calvin-Benson-Bassham cycle, yet isotopic discrimination by the CO₂ fixation enzyme, RubisCO (ribulose 1,5-bisphosphate carboxylase/oxygenase), has only been measured for a single marine cyanobacterium. Different forms of RubisCO occur in different phytoplankton species (overall amino acid identity varying by as much as ∼75%) and thus may vary in the degree to which they fractionate carbon. Here we measured isotope discrimination by RubisCO from the coccolithophore Emiliania huxleyi, a cosmopolitan species used as a marine algal model.E. huxleyi RubisCO discriminated substantially less (ε = 11.1‰) against ¹³CO₂ than other RubisCO enzymes (18-29‰), despite having Michaelis-Menten kinetic parameters (K_CO2 = 72 μM; V_max = 0.66 μmol min⁻¹ mg⁻¹ protein) similar to those measured for RubisCO enzymes from different organisms. If widespread, decreased isotope discrimination of ¹³C by phytoplankton RubisCO may be a major factor influencing the enriched ¹³C content of marine organic carbon. This finding emphasizes the necessity of (a) determining ε values for RubisCOs of other marine phytoplankton and (b) re-evaluation of δ¹³C values from physiological, environmental, and geological studies.     

Models of maar volcanoes,Lunar Crater (Nevada,USA)

Maar volcanoes are generally understood to be the result of highly energetic, explosive interaction between magma and water (groundwater or surface water). Two end-member conceptual models have been proposed to explain the dimensions (diameter, depth) of maar craters: (1) an incremental growth model, where a crater grows due to subsidence and ejection of debris over the course of many explosions, and the final size is an integrated result of multiple explosive events; (2) a model in which the dimensions of a maar crater are the result of the largest single explosion during the lifetime of the maar (major-explosion dominated model). In the latter case, the maar size can be used to estimate the energy and depth of the largest explosion, which in turn allows estimation of the magma mass involved. This paper describes Lunar Crater maar (Nevada, USA) and tests the two models as explanations for the characteristics of the volcano, in particular the major-explosion dominated model. This model implies magma mass and supply rates that are unrealistic, and the tephra at the maar do not contain key features observed in the ejecta at large single-explosion craters. The incremental growth model seems most suitable based upon geological evidence.     

The ebb and flood of Silica: Quantifying dissolved and biogenic silica fluxes from a temperate salt marsh

Salt marshes are widely studied due to the broad range of ecosystem services they provide including serving as crucial wildlife habitat and as hotspots for biogeochemical cycling. Nutrients such as nitrogen (N), phosphorus (P), and carbon (C) are well studied in these systems. However, salt marshes may also be important environments for the cycling of another key nutrient, silica (Si). Found at the land–sea interface, these systems are silica replete with large stocks in plant biomass, sediments, and porewater, and therefore, have the potential to play a substantial role in the transformation and export of silica to coastal waters. In an effort to better understand this role, we measured the fluxes of dissolved (DSi) and biogenic (BSi) silica into and out of two tidal creeks in a temperate, North American (Rowley, Massachusetts, USA) salt marsh. One of the creeks has been fertilized from May to September for six years allowing us to examine the impacts of nutrient addition on silica dynamics within the marsh. High-resolution sampling in July 2010 showed no significant differences in Si concentrations between the fertilized and reference creeks with dissolved silica ranging from 0.5 to 108 μM and biogenic from 2.0 to 56 μM. Net fluxes indicated that the marsh is a point source of dissolved silica to the estuary in the summer with a net flux of approximately 169 mol h⁻¹, demonstrating that this system exports DSi on the same magnitude as some nearby, mid-sized rivers. If these findings hold true for all salt marshes, then these already valuable regions are contributing yet another ecosystem service that has been previously overlooked; by exporting DSi to coastal receiving waters, salt marshes are actively providing this important nutrient for coastal primary productivity.     

The development of the Space Environment Viability of Organics (SEVO) experiment aboard the Organism/Organic Exposure to Orbital Stresses (O/OREOS) satellite

The Space Environment Viability of Organics (SEVO) experiment is one of two scientific payloads aboard the triple-cube satellite Organism/ORganic Exposure to Orbital Stresses (O/OREOS). O/OREOS is the first technology demonstration mission of the NASA Astrobiology Small Payloads Program. The 1-kg, 1000-cm³ SEVO cube is investigating the chemical evolution of organic materials in interstellar space and planetary environments by exposing organic molecules under controlled conditions directly to the low-Earth orbit (LEO) particle and electromagnetic radiation environment. O/OREOS was launched on November 19, 2010 into a 650-km, 72°-inclination orbit and has a nominal operational lifetime of six months. Four classes of organic compounds, namely an amino acid, a quinone, a polycyclic aromatic hydrocarbon (PAH), and a metallo-porphyrin are being studied. Initial reaction conditions were established by hermetically sealing the thin-film organic samples in self-contained micro-environments. Chemical changes in the samples caused by direct exposure to LEO radiation and by interactions with the irradiated microenvironments are monitored in situ by ultraviolet/visible/near-infrared (UV/VIS/NIR) absorption spectroscopy using a novel compact fixed-grating CCD spectrometer with the Sun as its light source. The goals of the O/OREOS mission include: (1) demonstrating key small satellite technologies that can enable future low-cost astrobiology experiments, (2) deploying a miniature UV/VIS/NIR spectrometer suitable for in-situ astrobiology and other scientific investigations, (3) testing the capability to establish a variety of experimental reaction conditions to enable the study of astrobiological processes on small satellites, and (4) measuring the chemical evolution of organic molecules in LEO under conditions that can be extrapolated to interstellar and planetary environments. In this paper, the science and technology development of the SEVO instrument payload and its measurements are described.     

Influence of Hydraulic Conductivity and Wellbore Design in the Fate and Transport of Nitrate in Multi-aquifer Systems

Nitrate concentrations in multi-aquifer systems are heavily affected by the presence of wellbores (active or abandoned) that are screened in several aquifers. The spatial variability of hydraulic conductivity in the confining layers has also an important impact on the concentrations. A synthetic three-dimensional flow and transport exercise was carried in a multi-aquifer system consisting of two aquifers separated by an aquitard in which 100 vertical wellbores had been drilled. To model the wellbores and the flow and transport connection between aquifers that they may induce, we assign a high vertical hydraulic conductivity and a low effective porosity to the cell blocks including the wells. With these parameters, a solute will travel quickly from one aquifer to the other without being stored in the well itself. The wellbores will act as preferential pathways, and the solute will move quickly between aquifers according to the hydrodynamic conditions. Not considering these preferential pathways could induce erroneous interpretations of the solute distribution in an aquifer. We also noted that when there are vertical wellbores that connect aquifers in a multi-aquifer system, low conductivity in the aquitard enhances the flow of solute through the wellbores. Time-varying pumping rates induce important fluctuations in nitrate concentrations; therefore, any estimate of the water quality of the aquifer will depend on the moment when the data has been recorded. Consequently, concentration maps obtained by interpolation of point samples are seldom a good indicator of the chemical status of groundwater bodies; alternatively, we recommend complementing the usual interpolated maps with numerical models to gain a true understanding of the spatial distribution of the solute concentration.