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Abstract. Antarctic meltwater is a significant source of iron that fertilizes present-day Southern Ocean ecosystems and may enhance marine carbon burial on geologic timescales. However, it remains uncertain how the nutrient flux from the subglacial system changes through time, particularly in response to climate, due to an absence of geologic records detailing element mobilization beneath ice sheets. In this study, we present a 25 kyr record of aqueous trace metal cycling in subglacial water beneath the David Glacier catchment measured in a subglacial chemical precipitate that formed across glacial termination III (TIII), from 259.5 to 225 ka. The deposition rate and texture of this sample describe a shift in subglacial meltwater flow following the termination. Alternating layers of opal and calcite deposited in the 10 kyr prior to TIII record centennial-scale subglacial flushing events, whereas reduced basal flushing resulted in slower deposition of a trace-metal-rich (Fe, Mn, Mo, Cu) calcite in the 15 kyr after TIII. This sharp increase in calcite metal concentrations following TIII indicates that restricted influx of oxygen from basal ice melt to precipitate-forming waters caused dissolution of redox-sensitive elements from the bedrock substrate. The link between metal concentrations and climate change in this single location across TIII suggests that ice motion may play an important role in subglacial metal mobilization and discharge, whereby heightened basal meltwater flow during terminations supplies oxygen to subglacial waters along the ice sheet periphery, reducing the solubility of redox-sensitive elements. As the climate cools, thinner ice and slower ice flow decrease subglacial meltwater production rates, limiting oxygen delivery and promoting more efficient mobilization of subglacial trace metals. Using a simple model to calculate the concentration of Fe in Antarctic basal water through time, we show that the rate of Antarctic iron discharge to the Southern Ocean is sensitive to this heightened mobility and may therefore increase significantly during cold climate periods. 

Abstract. Antarctic meltwater is a significant source of iron that fertilizes present-day Southern Ocean ecosystems and may enhance marine carbon burial on geologic timescales. However, it remains uncertain how this nutrient flux changes through time, particularly in response to climate, due to an absence of geologic records detailing trace metal mobilization beneath ice sheets. In this study, we present a 25 kyr record of aqueous trace metal cycling beneath the East Antarctic Ice Sheet measured in a subglacial chemical precipitate that formed across glacial termination III (TIII). The deposition rate and texture of this sample describe a shift in basal meltwater flow following the termination. Alternating layers of opal and calcite deposited in the 10 kyr prior to TIII record centennial-scale subglacial flushing events, whereas reduced basal flushing resulted in slower deposition of a trace metal-rich (Fe, Mn, Mo, Cu) calcite in the 15 kyr after TIII. This sharp increase in calcite metal concentrations following TIII indicates that diminished subglacial meltwater flow restricted the influx of oxygen from basal ice melt to precipitate-forming waters, causing dissolution of redox-sensitive trace metals from the bedrock substrate. These results are consistent with a possible feedback between orbital climate cycles and Antarctic subglacial iron discharge to the Southern Ocean, whereby heightened basal meltwater flow during terminations supplies oxygen to subglacial waters along the ice sheet periphery, which reduces the solubility of redox sensitive elements. As the climate cools, thinner ice and slower ice flow reduce basal meltwater production rates, limiting oxygen delivery and promoting more efficient mobilization of subglacial trace metals. Using a simple model to calculate the concentration of Fe in Antarctic basal water through time, we show that the rate of Antarctic iron discharge to the Southern Ocean is highly sensitive to this heightened mobility, and may therefore, increase significantly during cold climate periods. 

Abstract Magmatic gas exsolving during late-stage cooling of shallow magmas has been considered an important facilitator of low-pressure alteration and metal transport. However, the chemical properties of such gas, particularly its metal transport mechanisms and capacity, remain elusive. Trace elements in minerals produced by gas-mediated surface reaction or precipitation from gas capture details of gas composition and reaction pathways. However, interpretation of mineral trace element contents is dependent on understanding crystallographic controls on gas/mineral partitioning. This work investigates the structural accommodation of As, Mn, Ga, Ge, Fe, and Ti in vapor-deposited topaz of vesicular topaz rhyolite from the Thomas Range, Utah, through single-crystal synchrotron microbeam X-ray techniques on picogram quantities of those trace elements. X-ray absorption near edge structure (XANES) data indicates that these elements are incorporated into topaz as As5+, Fe3+, Mn3+, Ti4+, Ga3+, and Ge4+. Extended X-ray absorption fine structure (EXAFS) analysis for these trace elements, compared to EXAFS of structural Al and Si, reveals that As5+ and Ge4+ are incorporated directly into the tetrahedral site of the topaz structure, with the octahedral site accommodating Mn3+, Fe3+, Ga3+, and Ti4+. For As5+ and Fe3+, the structural impact of substitution extends to at least second neighbors (other elements were only resolvable to first neighbors). Further interpretation of the EXAFS results suggests that the substitution of Ti4+ results in increased distortion of the octahedral site, while the other trace elements induce more uniform expansion correlating in magnitude to their ionic radius. Comparison of quantified X-ray fluorescence (XRF) data for two topaz crystals from this rhyolite reveals variable trace element concentrations for As5+, Fe3+, Ga3+, and Ti4+, reflective of a source gas undersaturated in these trace elements changing in concentration over the period of topaz deposition. The identical Ge4+ content of the two topaz crystals suggests that Ge4+ in the gas was buffered by the growth of another Ge4+-bearing phase, such as quartz. The very low Mn3+ content in the topaz crystals does not reflect the abundance of Mn3+ in the gas (saturation of Mn is evidenced by coexisting bixbyite). Instead, it suggests a strong Jahn-Teller inhibitory effect to the substitution of Mn3+ for Al3+ in the distorted octahedral site of topaz. It is proposed that exsolution of an HF-enriched gas from cooling rhyolitic magma led to local scouring of Al, Si, and trace metals from the magma. Once topaz crystals nucleated, self-catalyzed reactions that recycle HF led to continued growth of topaz. 

Synchrotron instruments are useful for marine studies because they make nondestructive measurements of chemical composition and speciation on small sample volumes and at low concentrations. Synchrotron beamtime is available without cost using a peer-reviewed proposal system. New users do not have to be synchrotron radiation experts to design a good experiment, but some guidance is needed to design and propose appropriate experiments. Here we present some of that guidance to encourage and increase access to synchrotron facilities for marine science. We provide advice and examples from experts on how to access these instruments, choose the optimal sample preparation, and avoid common pitfalls. We then present some examples of successful marine studies that use these techniques. 

Abstract Ice cores and offshore sedimentary records demonstrate enhanced ice loss along Antarctic coastal margins during millennial-scale warm intervals within the last glacial termination. However, the distal location and short temporal coverage of these records leads to uncertainty in both the spatial footprint of ice loss, and whether millennial-scale ice response occurs outside of glacial terminations. Here we present a >100kyr archive of periodic transitions in subglacial precipitate mineralogy that are synchronous with Late Pleistocene millennial-scale climate cycles. Geochemical and geochronologic data provide evidence for opal formation during cold periods via cryoconcentration of subglacial brine, and calcite formation during warm periods through the addition of subglacial meltwater originating from the ice sheet interior. These freeze-flush cycles represent cyclic changes in subglacial hydrologic-connectivity driven by ice sheet velocity fluctuations. Our findings imply that oscillating Southern Ocean temperatures drive a dynamic response in the Antarctic ice sheet on millennial timescales, regardless of the background climate state. 

Abstract Numerous studies have documented rare-earth element (REE) mobility in hydrothermal and metamorphic fluids, but the processes and timing of REE mobility are rarely well constrained. The Round Top laccolith in the Trans-Pecos magmatic province of west Texas, a REE ore prospect, has crosscutting fractures filled with fluorite and calcite along with a variety of unusual minerals. Most notably among these is an yttrium and heavy rare-earth element (YHREE) carbonate mineral, which is hypothesized to be lokkaite based on elemental analyses. While the Round Top laccolith is dated to 36.2 ± 0.6 Ma based on K/Ar in biotite, U-Pb fluorite and nacrite ages presented here clearly show the mineralization in these veins is younger than 6.2 ± 0.4 Ma (the age of the oldest fluorite). This discrepancy in dates suggests that fluids interacted with the laccolith to mobilize REE more than 30 m.y. after igneous emplacement. The timing of observed REE mobilization overlaps with Rio Grande rift extension, and we suggest that F-bearing fluids associated with extension may be responsible for initial mobilization. A later generation of fluids was able to dissolve fluorite, and we hypothesize this later history involved sulfuric acid. Synchrotron spectroscopy and laser ablation–inductively coupled plasma–mass spectrometry (LA-ICP-MS) U-Pb dating of minerals that record these fluids offer tremendous potential for a more fundamental understanding of processes that are important not only for REE but other ore deposits as well.