Sequential Separation of Uranium, Hafnium and Neodymium from Natural Waters Concentrated by Iron Coprecipitation

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/111909/1/ggr12049-sup-0002-TableS1.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/111909/2/ggr12049-sup-0003-TableS2.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/111909/3/ggr12049-sup-0008-TableS7.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/111909/4/ggr12049-sup-0001-FigS1.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/111909/5/ggr12049.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/111909/6/ggr12049-sup-0004-TableS3.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/111909/7/ggr12049-sup-0005-TableS4.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/111909/8/ggr12049-sup-0006-TableS5.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/111909/9/ggr12049-sup-0007-TableS6.pd

Noble gas signatures in Greenland : tracing glacial meltwater sources

Author Posting. © American Geophysical Union, 2015. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geophysical Research Letters 42 (2015): 9311–9318, doi:10.1002/2015GL065778.This study represents the first comprehensive noble gas study in glacial meltwater from the Greenland Ice Sheet. It shows that most samples are in disequilibrium with surface collection conditions. A preliminary Ne and Xe analysis suggests that about half of the samples equilibrated at a temperature of ~0°C and altitudes between 1000 m and 2000 m, with a few samples pointing to lower equilibration altitudes and temperatures between 2°C and 5°C. Two samples suggest an origin as melted ice and complete lack of equilibration with surface conditions. A helium component analysis suggests that this glacial meltwater was isolated from the atmosphere prior to the 1950s, with most samples yielding residence times ≤ 420 years. Most samples represent a mixture between a dominant atmospheric component originating as precipitation and basal meltwater or groundwater, which has accumulated crustal 4He over time.University of Michigan; Packard Foundation; Department of Earth and Environmental Sciences Turner fellowship2016-05-0

Microbial communities of the Lemon Creek Glacier show subtle structural variation yet stable phylogenetic composition over space and time

Glaciers are geologically important yet transient ecosystems that support diverse, biogeochemically significant microbial communities. During the melt season glaciers undergo dramatic physical, geochemical and biological changes that exert great influence on downstream biogeochemical cycles. Thus, we sought to understand the temporal melt-season dynamics of microbial communities and associated geochemistry at the terminus of Lemon Creek Glacier (LCG) in coastal southern Alaska. Due to late season snowfall, sampling of LCG occurred in three interconnected areas: proglacial Lake Thomas, the lower glacial outflow stream and the glacier’s terminus. LCG associated microbial communities were phylogenetically diverse and varied by sampling location. However, Betaproteobacteria, Alphaproteobacteria and Bacteroidetes dominated communities at all sampling locations. Strict anaerobic groups such as methanogens, SR1, and OP11 were also recovered from glacier outflows, indicating anoxic conditions in at least some portions of the LCG subglacial environment. Microbial community structure was significantly correlated with sampling location and sodium concentrations. Microbial communities sampled from terminus outflow waters exhibited day-to-day fluctuation in taxonomy and phylogenetic similarity. However, these communities were not significantly different from randomly constructed communities from all three sites. These results indicate that glacial outflows share a large proportion of phylogenetic overlap with downstream environments and that the observed significant shifts in community structure are driven by changes in relative abundance of different taxa, and not complete restructuring of communities. We conclude that LCG glacial discharge hosts a diverse and relatively stable microbiome that shifts at fine taxonomic scales in response to geochemistry and likely water residence time

An open source Bayesian Monte Carlo isotope mixing model with applications in Earth surface processes

The implementation of isotopic tracers as constraints on source contributions has become increasingly relevant to understanding Earth surface processes. Interpretation of these isotopic tracers has become more accessible with the development of Bayesian Monte Carlo (BMC) mixing models, which allow uncertainty in mixing end‐members and provide methodology for systems with multicomponent mixing. This study presents an open source multiple isotope BMC mixing model that is applicable to Earth surface environments with sources exhibiting distinct end‐member isotopic signatures. Our model is first applied to new δ18O and δD measurements from the Athabasca Glacier, which showed expected seasonal melt evolution trends and vigorously assessed the statistical relevance of the resulting fraction estimations. To highlight the broad applicability of our model to a variety of Earth surface environments and relevant isotopic systems, we expand our model to two additional case studies: deriving melt sources from δ18O, δD, and 222Rn measurements of Greenland Ice Sheet bulk water samples and assessing nutrient sources from ɛNd and 87Sr/86Sr measurements of Hawaiian soil cores. The model produces results for the Greenland Ice Sheet and Hawaiian soil data sets that are consistent with the originally published fractional contribution estimates. The advantage of this method is that it quantifies the error induced by variability in the end‐member compositions, unrealized by the models previously applied to the above case studies. Results from all three case studies demonstrate the broad applicability of this statistical BMC isotopic mixing model for estimating source contribution fractions in a variety of Earth surface systems.Key Points:Open source BMC model determines source contributions in Earth surface systemsEffectively applied to stable and radiogenic isotope systems in various settingsModel able to encompass end‐member uncertainties and multiple isotopic systemsPeer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/111937/1/ggge20708.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/111937/2/ggge20708-sup-0001-2014GC005683-ts01.pd

Increased Arctic NO3− Availability as a Hydrogeomorphic Consequence of Permafrost Degradation and Landscape Drying

Climate-driven permafrost thaw alters the strongly coupled carbon and nitrogen cycles within the Arctic tundra, influencing the availability of limiting nutrients including nitrate (NO3−). Researchers have identified two primary mechanisms that increase nitrogen and NO3− availability within permafrost soils: (1) the ‘frozen feast’, where previously frozen organic material becomes available as it thaws, and (2) ‘shrubification’, where expansion of nitrogen-fixing shrubs promotes increased soil nitrogen. Through the synthesis of original and previously published observational data, and the application of multiple geospatial approaches, this study investigates and highlights a third mechanism that increases NO3− availability: the hydrogeomorphic evolution of polygonal permafrost landscapes. Permafrost thaw drives changes in microtopography, increasing the drainage of topographic highs, thus increasing oxic conditions that promote NO3− production and accumulation. We extrapolate relationships between NO3− and soil moisture in elevated topographic features within our study area and the broader Alaskan Coastal Plain and investigate potential changes in NO3− availability in response to possible hydrogeomorphic evolution scenarios of permafrost landscapes. These approximations indicate that such changes could increase Arctic tundra NO3− availability by ~250–1000%. Thus, hydrogeomorphic changes that accompany continued permafrost degradation in polygonal permafrost landscapes will substantially increase soil pore water NO3− availability and boost future fertilization and productivity in the Arctic

Dust composition changes from Taylor Glacier (East Antarctica) during the last glacial-interglacial transition: A multi-proxy approach

Mineral dust is transported in the atmosphere and deposited in oceans, ice sheets and the terrestrial biosphere. Temporal changes in locations of dust source areas and transport pathways have implications for global climate and biogeochemical cycles. The chemical and physical characterization of the dust record preserved in ice cores is useful for identifying of dust source regions, dust transport, dominant wind direction and storm trajectories. Here, we present a 50,000-year geochemical characterization of mineral dust entrapped in a horizontal ice core from the Taylor Glacier in East Antarctica. Strontium (Sr) and neodymium (Nd) isotopes, grain size distribution, trace and rare earth element (REE) concentrations, and inorganic ion (Cl− and Na+) concentrations were measured in 38 samples, corresponding to a time interval from 46 kyr before present (BP) to present. The Sr and Nd isotope compositions of insoluble dust in the Taylor Glacier ice shows distinct changes between the Last Glacial Period (LGP in this study ranging from ∼46.7–15.3 kyr BP) the early Holocene (in this study ranging from ∼14.5–8.7 kyr BP), and zero-age samples. The 87Sr/86Sr isotopic composition of dust in the Taylor Glacier ice ranged from 0.708 to 0.711 during the LGP, while the variability during the early Holocene is higher ranging from 0.707 to 0.714. The εNd composition ranges from 0.1 to −3.9 during the LGP, and is more variable from 1.9 to −8.2 during the early Holocene. The increased isotopic variability during the early Holocene suggests a shift in dust provenance coinciding with the major climate transition from the LGP to the Holocene. The isotopic composition and multiple physical and chemical constraints support previous work attributing Southern South America (SSA) as the main dust source to East Antarctica during the LGP, and a combination of both local Ross Sea Sector dust sources and SSA after the transition into the Holocene. This study provides the first high time resolution data showing variations in dust provenance to East Antarctic ice during a major climate regime shift, and we provide evidence of changes in the atmospheric transport pathways of dust following the last deglaciation