02885nas a2200241 4500008004100000245006300041210006200104260004100166300001200207520209300219653003102312653003602343653002402379653001902403653002402422100001602446700001702462700002302479700001702502700002402519700002502543856007502568 2021 eng d00aChemical weathering in the McMurdo Dry Valleys, Antarctica0 aChemical weathering in the McMurdo Dry Valleys Antarctica aHoboken, NJbJohn Wiley & Sons, Inc. a205-2163 a

While chemical weathering has not always been considered an active process in the McMurdo Dry Valleys (MDV), Antarctica, long‐term geochemical and hydrological investigations have provided an overall better understanding of chemical weathering in this polar desert environment. Liquid water on the landscape is limited to stream channels as well as shallow subsurface melt features, as there is no overland flow. Stream total suspended sediment loads are low, with the sources of sediment from stream channels, aeolian input, and/or from the surfaces of glaciers. MDV soils contain high concentrations of soluble salts with little clay material, but since absent of water, these soils are a minimal location of chemical weathering. Hyporheic zones exchange water during streamflow, and these areas control the stream geochemistry over various temporal scales. Hyporheic zones promote rapid aluminosilicate weathering by moving dilute glacial meltwater into intimate contact with sediment surfaces. Rapid weathering of the aluminosilicates in the streambed and hyporheic zones is the most plausible explanation for chemostasis observed in these streams, indicating that little to no catchment processes are necessary to explain the observed chemostasis in the MDV. Shallow subsurface waters with distinct geochemical signatures have much higher dissolved Si concentrations than the stream waters and indicate that they are responsible for enhanced aluminosilicate weathering in this polar desert environment. The dissolution of CaCO3 is also a major process in the hyporheic zones as generally the streams are unsaturated with respect to calcite. Cation‐exchange reactions are also important in the evolution from Na‐Cl brines to Ca‐Cl brines within the soil column, while authigenic CaCO3 can both dissolve and precipitate depending on the condition of the system. Recently, stream channel landscapes are changing due to the melting of buried ice, creating thermokarst and water track features, resulting in a sediment and solute influx to the stream.

10aaluminosilicate weathering10aCaCO3 dissolution/precipitation10achemical weathering10ahyporheic zone10aMcMurdo Dry Valleys1 aHunt, Allen1 aEgli, Markus1 aFaybishenko, Boris1 aLyons, Berry1 aLeslie, Deborah, L.1 aGooseff, Michael, N. uhttps://agupubs.onlinelibrary.wiley.com/doi/10.1002/9781119563952.ch1102509nas a2200205 4500008004100000245012600041210006900167260005300236490000900289520180200298653002502100653001502125653001702140653002402157653002002181653002302201100002502224700001702249856003702266 2020 eng d00aAnalysis of acid-leachable barium, copper, iron, lead, & zinc concentrations in Taylor Valley, Antarctic stream sediments0 aAnalysis of acidleachable barium copper iron lead zinc concentra aColumbus, OHbThe Ohio State Universityc05/20200 vB.S.3 a

The purpose of this study is to assess the concentrations of Barium (Ba), Copper (Cu), Iron (Fe), Lead (Pb), and Zinc (Zn) in sediment samples obtained from the Wales and Commonwealth streams located in Taylor Valley, Antarctica. These samples were collected at seven sample sites (three in Wales Glacier and four in Commonwealth Glacier) in 0 to 2 cm, 2 to 4 cm, 4 to 6 cm, and 6 to 8 cm depth increments which resulted in 28 total samples. After the collection process, these samples underwent a volumetric 1:5 sediment: 10% HCl leach for 48 hours, filtration through 4-µm pore-size, cellulose acetate membrane filters, and inductively coupled plasma mass spectrometry (ICP-MS) analyses in the Trace Element Research Laboratory at The Ohio State University. Upon completion of the analyses, results showed that the Wales samples had a higher average concentration of every metal element overall and at each depth increment when compared to the Commonwealth samples. In addition to the weak-acid leachate metal analyses, a second aliquot of one sediment profile from each stream was analyzed at Villanova University for the 210Pb activity via gamma spectroscopy. This was done to estimate the sedimentation rates at each of these sites. From the sedimentation rates, sedimentation fluxes were calculated for each element for each sediment profile at each of these sites. The data demonstrated that Fe is the most abundant element while Pb is the least abundant. Lastly, upon examination of results, it was found that the concentrations of these metals are often higher in samples collected closer to the surface. These findings suggest these streams, and their sources, have had little, if any, impact by anthropogenic input of metals, and that metal fluxes to the sediments are low.

10aacid-leachable metal10aAntarctica10ageochemistry10aMcMurdo Dry Valleys10apolar sediments10asedimentation rate1 aPiergallini, Brianna1 aLyons, Berry uhttp://hdl.handle.net/1811/9177202094nas a2200241 4500008004100000245014400041210006900185260001200254490000600266520131100272653002001583653001401603653001701617653001501634653001501649653002401664653001301688653002201701100001701723700002201740700002401762856006601786 2018 eng d00aThe impact of fossil fuel burning related to scientific activities in the McMurdo Dry Valleys, Antarctica: Revisited0 aimpact of fossil fuel burning related to scientific activities i c04/20180 v63 a

 

Fossil fuel use associated with scienti c activities in the Taylor Valley, Antarctic has been examined to determine the fluxes of particulate organic and elemental carbon and nitrogen as well as NOx for the 2015–2016 austral summer field season. These carbon and nitrogen fluxes are compared to our previously published calculations for the 1997–1998 austral summer. In addition, we compile fossil fuel usage and resulting C and N fluxes from the major field camp in Taylor Valley, Lake Hoare Camp (LHC) from the late 1990’s through 2017. In general, the annual fluxes do vary from year to year, but there is no significant trend, at least during the primary summer field season. There is indication that increasing the length of scientific operations does increase the C and N inputs via fossil fuel burning. This works supports our original results demonstrating that over long periods of time the anthropogenic flux of N from local fossil fuel burning could become quantitatively important in the region. Although the particulate C fluxes remain very low, the recent finding of black carbon in the Taylor Valley landscape indicates more on-going monitoring of the source of this material is merited.

 

10acarbon dynamics10aemissions10afossil fuels10ahelicopter10amanagement10aMcMurdo Dry Valleys10anitrogen10ascience activites1 aLyons, Berry1 aSaelens, Elsa, D.1 aWelch, Kathleen, A. uhttps://www.elementascience.org/article/10.1525/elementa.288/03970nas a2200217 4500008004100000245011000041210007200151260004000223490001000263520322300273653001503496653001903511653001903530653002403549653003003573653003703603653001603640100001703656700001703673856006203690 2013 eng d00aThe application of stable isotopes, δ11B, δ18O, and δD, in geochemical and hydrological investigations0 aapplication of stable isotopes δ11B δ18O and δD in geochemical a aColumbus, OHbOhio State University0 vPh.D.3 a

My dissertation research utilizes stable isotopes as tracers of water and solute sources to study specific geochemical (solute origin) and hydrological (glacier meltwater source across a season comparing water contributions from hyporheic zone and/or glacier melt and residence time of precipitation within a managed water supply) problems within McMurdo Dry Valleys (MCM), Antarctica, and Central Ohio, USA. In Chapter II, δ11B isotopic and dissolved B measurements are used to infer the origin of B within MCM aquatic system. Boron stable isotopic values span the range of +12.3‰ to +51.4‰, varying from glacier meltwater streams to the hypolimnion of a highly evaporated hypersaline lake. These data demonstrate that the major sources of B are chemical weathering of alumniosilicates within the stream channels, and a marine source, either currently introduced by marine-derived aerosols or from ancient seawater. In-lake processes create a more positive δ11B through adsorption or mineral precipitation. The glacier meltwater streams, Lakes Fryxell, Hoare, and upper waters of Lake Joyce display a mixture of these two sources, with Lake Joyce bottom waters primarily of marine origin. Lakes Bonney and Vanda and Blood Falls brine are interpreted as having a marine-like source changed by in-lake processes to result in a more positive δ11B, while Don Juan Pond displays a more terrestrial influence. In Chapter III, δ18O and δD are used to trace water source variation via hyporheic zone or glacier melt within two MCM streams over an entire melt season. The isotopic variation of these streams was more negative at the beginning of the season and more positive later. D-excess measurements were used to infer mixing between hyporheic storage and glacier meltwater. It was supported that Von Guerard Stream has a large, widespread hyporheic zone that changes with time and discharge amounts. The chemistry of Andersen Creek also displayed hyporheic zone influence at certain times of the year. This work adds important new information on the role of hyperheic zone-stream interactions, and supports the short term, more physically based, descriptions of hyporheic dynamics explained in the past decade. Chapter IV describes water flow and travel time within a human managed watershed-reservoir system by measuring the δ18O and δD of the precipitation source to the reservoirs and finally to the distribution system, the tap. Generally, the tap waters experienced little lag time in the managed system, having a residence time of about two months. Tap and reservoir waters preserved the precipitation signal with the reservoir morphology acting as an important control. These water supply reservoirs functioned more like a river system with a faster throughput of water and larger variations in chemical parameters. Other water supply reservoirs have a greater capacity with a larger amount of water supply usage through a more lacustrine environment, which displays more constant solute concentrations and longer flow-through times. This work provides a basic understanding of a regional water supply system in central Ohio, reservoir isotopic dynamics, and Ohio precipitation sources.

10aAntarctica10aboron isotopes10ahyporheic zone10aMcMurdo Dry Valleys10aOhio precipitation source10aoxygen-18 and deuterium isotopes10asaline lake1 aLeslie, D.L.1 aLyons, Berry u http://rave.ohiolink.edu/etdc/view?acc_num=osu138600003705611nas a2200229 4500008004100000245006100041210006000102260004000162490000900202520491500211653002205126653001505148653000905163653002605172653001705198653002405215653002405239653001505263100002505278700001705303856006105320 2010 eng d00aAeolian sediments of the McMurdo Dry Valleys, Antarctica0 aAeolian sediments of the McMurdo Dry Valleys Antarctica aColumbus, OHbOhio State University0 vM.S.3 a

The role of dust has become a topic of increasing interest in the interface between climate and geological/ecological sciences. Dust emitted from major sources, the majority of which are desert regions in the Northern Hemisphere, is transported via suspension in global wind systems and incorporated into the biogeochemical cycles of the ecosystems where it is ultimately deposited. While emissions within the McMurdo Dry Valleys (MDV) region of Antarctica are small compared to other source regions, the redistribution of new, reactive material by wind may be important to sustaining life in the ecosystem.


The interaction of the dry, warm foehn winds and the cool, moist coastal breezes “recycles” soil particles throughout the landscape. The bulk of sediment movement occurs during foehn events in the winter that redistribute material throughout the MDV. To understand the source and transfer of this material samples were collected early in the austral summer (November 2008) prior to the initiation of extensive ice melt from glacial and lake surfaces, aeolian landforms, and elevated sediment traps. These were preserved and processed for grain size distribution and major element composition at the sand and silt particle sizes. Major elemental oxide analysis indicated that the silt and sand size particles are of different composition: SiO2 values for silt range from 50 to 59% by weight and for sand range from 59 to 74%. When compared to the elemental oxide composition four rock types present in the MDV, the composition of the silt indicates a mixing influenced mostly by the igneous rock types (Ferrar Dolerite and McMurdo Volcanic basanite) and sand a mixing influenced largely by the sedimentary rocks (Beacon Sandstone and the metasedimentary Basement Complex). This could imply a local source of the aeolian material that is corroborated by low CIA values at both particle sizes (44-57%) indicating low degrees of chemical weathering. In addition, comparison of 87Sr/86Sr and 143Nd/144Nd to values published for the major MDV rock types and ice core dust to values analyzed in 3 silt size glacier sample and one bulk glacier sample also indicates a local source of sediments and that it is not likely to be transferred inland.


During the melt season, the aeolian material is actively solubilized where it interacts with water, releasing solutes and vital bioavailable nutrients throughout the aquatic system. Differences in the chemistry of supra- and proglacial streams as well as lake surface waters may be derived from the deposition and dissolution of these aeolian sediments. To simulate these conditions, a two-step leaching method using deionized water to represent glacial melt in field conditions was employed and leachates analyzed for major ion and nutrient constituents. Leachates represent a small degree (<0.7%) of dissolution of major elements, and are solubilized to a greater extent from samples closer to the coast or with increased silt content. The composition of the leachates reflects the dissolution of the major salts found in the MDV. Leach 1 (cold water) indicates that Na- and Cl-bearing salt phases are dissolved to a greater extent than seen in Leach 2 (freeze-thaw). Conversely, Leach 2 compositions indicate that carbonate mineral dissolution and Mg-bearing silicate weathering are proceeding to a greater extent than in Leach 1.


Inorganic N:P ratios follow the same patterns of nutrient limitations based on the Redfield Ratio found by Priscu (1995) in the terminal lakes of the Taylor Valley: N-limited in the Fryxell and Hoare basins (east) and P-limited in the Bonney basin (west). This is also consistent with the age of the tills in the area, as found by Gudding (2003). The concentration of soluble Fe in the leachates is about the same as soluble inorganic P, and thus is not a limiting nutrient in the leachates. Comparison of total dissolved N and P to their inorganic counterparts reveals increased organic nutrients in the glacier and lake leachates that may indicate the influence of biota. Nutrient fluxes based on known sediment fluxes from elevated sediment traps deployed throughout the MDV and the composition of these leachates range from 0.34-330 g a-1 for N, 0.02-8.3 g a-1 for P, and 0.03-8.6 g a-1 for Fe. These are at least two orders of magnitude less than calculated loads from streams to the lakes in the Taylor Valley and, thus, should be considered underestimations or minima.


This work provides the first investigation into the composition and source of aeolian transported materials in the MDV, as well of what is potentially solubilized from it during the austral summer melt season. In addition, it will contribute to the understanding of the interplay between aeolian and aquatic processes in the MDV and further the understanding of this unique ecosystem.

10aaeolian transport10aAntarctica10adust10aexperimental leaching10ageochemistry10aMcMurdo Dry Valleys10asediment provenance10aweathering1 aDeuerling, Kelly, M.1 aLyons, Berry uhttp://rave.ohiolink.edu/etdc/view?acc_num=osu1290524862