Scholarly Work - Land Resources & Environmental Sciences
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Item Geomicrobiology of Blood Falls: An iron-rich saline discharge at terminus of the Taylor Glacier, Antarctica(2004-09) Mikucki, Jill A.; Foreman, Christine M.; Sattler, Birgit; Lyons, W. Berry; Priscu, John C.Blood Falls, a saline subglacial discharge from the Taylor Glacier, Antarctica provides an example of the diverse physical and chemical niches available for life in the polar desert of the McMurdo Dry Valleys. Geochemical analysis of Blood Falls outflow resembles concentrated seawater remnant from the Pliocene intrusion of marine waters combined with products of weathering. The result is an iron-rich, salty seep at the terminus of Taylor Glacier, which is subject to episodic releases into permanently ice-covered Lake Bonney. Blood Falls influences the geochemistry of Lake Bonney, and provides organic carbon and viable microbes to the lakesystem. Here we present the first data on the geobiology of Blood Falls and relate it to the evolutionary history of this unique environment. The novel geological evolution of this subglacial environment makes Blood Falls an important site for the study of metabolic strategies in subglacial environments and the impact of subglacial efflux on associated lake ecosystems.Item Impact of episodic warming events(2004-09) Foreman, Christine M.; Wolf, Craig F.; Priscu, John C.Lakes in the Taylor Valley, Antarctica, were investigated to determine the impact of a significant air temperature warming event that occurred during the austral summer of 2001–2002. The warming in the valleys caused an increase in glacial run-off, record stream discharge, an increase in lake levels, and thinning of the permanent ice covers. These changes in the physical environment drove subsequent changes in the biogeochemistry of the lakes. Primary production in West Lake Bonney during the flood was reduced 23% as a consequence of stream induced water column turbidity. Increased nutrient levels within the lakes occurred in the year following the temperature induced high flow year. For example, soluble reactive phosphorus loading to Lake Fryxell was four-fold greater than the long-term average loading rates. These high nutrient levels corresponded to an increase in primary production in the upper water columns of Lakes Bonney and Fryxell. Depth integrated chlorophyll-a values increased 149% in East Lake Bonney, 48% in West Lake Bonney, and showed little change in Lake Fryxell; chlorophyll-a in Lake Hoare decreased 18% compared to long-term averages recorded as part of our ten year monitoring program, presumably from a reduction in under-ice PAR caused by increased sediment loads on the ice cover. Overall the warming event served to recharge the ecosystem with liquid water and associated nutrients. Such floods may play an important role in the long-term maintenance of liquid water in these dry valley lakes.Item Glacial ice cores: A model system for developing extraterrestrial decontamination protocols(2005-04) Christner, Brent C.; Mikucki, Jill A.; Foreman, Christine M.; Denson, Jackie; Priscu, John C.Evidence gathered from spacecraft orbiting Mars has shown that water ice exists at both poles and may form a large subsurface reservoir at lower latitudes. The recent exploration of the martian surface by unmanned landers and surface rovers, and the planned missions to eventually return samples to Earth have raised concerns regarding both forward and back contamination. Methods to search for life in these icy environments and adequate protocols to prevent contamination can be tested with earthly analogues. Studies of ice cores on Earth have established past climate changes and geological events, both globally and regionally, but only recently have these results been correlated with the biological materials (i.e., plant fragments, seeds, pollen grains, fungal spores, and microorganisms) that are entrapped and preserved within the ice. The inclusion of biology into ice coring research brings with it a whole new approach towards decontamination. Our investigations on ice from the Vostok core (Antarctica) have shown that the outer portion of the cores have up to 3 and 2 orders of magnitude higher bacterial density and dissolved organic carbon (DOC) than the inner portion of the cores, respectively, as a result of drilling and handling. The extreme gradients that exist between the outer and inner portion of these samples make contamination a very relevant aspect of geomicrobiological investigations with ice cores, particularly when the actual numbers of ambient bacterial cells are low. To address this issue and the inherent concern it raises for the integrity of future investigations with ice core materials from terrestrial and extraterrestrial environments, we employed a procedure to monitor the decontamination process in which ice core surfaces are painted with a solution containing a tracer microorganism, plasmid DNA, and fluorescent dye before sampling. Using this approach, a simple and direct method is proposed to verify the authenticity of geomicrobiological results obtained from ice core materials. Our protocol has important implications for the design of life detection experiments on Mars and the decontamination of samples that will eventually be returned to Earth.Item Biological materials in ice cores(2006) Priscu, John C.; Christner, Brent C.; Foreman, Christine M.; Royston-Bishop, GeorgeItem Limnological conditions in subglacial Lake Vostok, Antarctica(2006-11) Christner, Brent C.; Royston-Bishop, George; Foreman, Christine M.; Arnold, Brianna R.; Tranter, Martyn; Welch, Kathleen A.; Lyons, W. Berry; Tsapin, Alexandre I.; Studinger, Michael; Priscu, John C.Subglacial Lake Vostok is located ~4 km beneath the surface of the East Antarctic Ice Sheet and has been isolated from the atmosphere for >15 million yr. Concerns for environmental protection have prevented direct sampling of the lake water thus far. However, an ice core has been retrieved from above the lake in which the bottom ~85 m represents lake water that has accreted (i.e., frozen) to the bottom of the ice sheet. We measured selected constituents within the accretion ice core to predict geomicrobiological conditions within the surface waters of the lake. Bacterial density is two- to sevenfold higher in accretion ice than the overlying glacial ice, implying that Lake Vostok is a source of bacterial carbon beneath the ice sheet. Phylogenetic analysis of amplified small subunit ribosomal ribonucleic acid (rRNA) gene sequences in accretion ice formed over a deep portion of the lake revealed phylotypes that classify within the β-, y-, and δ-Proteobacteria. Cellular, major ion, and dissolved organic carbon levels all decreased with depth in the accretion ice (depth is a proxy for increasing distance from the shoreline), implying a greater potential for biological activity in the shallow shoreline waters of the lake. Although the exact nature of the biology within Lake Vostok awaits direct sampling of the lake water, our data from the accretion ice support the working hypothesis that a sustained microbial ecosystem is present in this subglacial lake environment, despite high pressure, constant cold, low nutrient input, potentially high oxygen concentrations, and an absence of sunlight.Item Metabolic activity and diversity of cyoconites in the Taylor Valley, Antarctica(2007-12) Foreman, Christine M.; Sattler, Birgit; Mikucki, Jill A.; Porazinska, D. L.; Priscu, John C.Metabolic activity and biogeochemical diversity within cryoconites from the Canada,Commonwealth, Howard, and Hughes glaciers in the McMurdo Dry Valleys revealed the presence of a productive microbial refuge in this polar desert ecosystem. Fluorescent in situ hybridization showed a high percentage of Cytophaga-Flavobacteria cells in cryoconite sediments (87.2%), while β-Proteobacterial cells dominated the ice overlying the sediment layer (54.2%). The biomass of bacterial cells in the sediments was also greater (4.82 µgC ml-1) than that in the overlying ice (0.18 mgC ml-1) and was related to bacterial productivity (on the basis of thymidine incorporation), which ranged from 36 ng C l-1 d-1 in the overlying ice to 3329 ng C l-1 d -1 in the sediment-containing layers. Bacteria within both the sediments and overlying ice were able to actively incorporate and respire radio-labeled glucose, as well as 17 other dissolved organic carbon compounds. The cryoconites in the Taylor Valley support an active, diverse assemblage of organisms despite the fact that they may remain sealed from the atmosphere for decades. Given the density of the cryoconites in the dry valleys ( ~4–6% of ablation zone surfaces), flushing of the cryoconites during warm years could provide a vital nutrient and organic carbon source to the surrounding polar desert.Item Lakes of Antarctica(2009) Priscu, John C.; Foreman, Christine M.Introduction:The evolutionary history of Antarctic lakes reflects the history of the continent itself. More than 170 Mya, Antarctica was part of the supercontinent Gondwana. Over time Gondwana broke apart and Antarctica, as we know it today, was formed around 25 Mya. During its evolution, the continent underwent numerous climate shifts. Around 65 Mya, Antarctica still had a tropical to subtropical climate, complete with an Australasian flora and fauna. Ice first began to appear around 40 Mya. The opening of the Drake Passage between Antarctica and South America around 23 Mya resulted in the Antarctic Circumpolar Current, which effectively isolated the advection of lower latitude warm water to the region, leading to continent-scale glaciations that now typify Antarctica. The period between 14.8 and 13.6 Mya (mid Miocene) saw an important change in the landscape evolution. During this time, the linked climate and-glacial system changed from one dominated by intermittent fluvial erosion and wet-based glaciation, to one featuring a largely cold-based ice sheet, with cold-based alpine glaciers in the hyperarid, cold desert conditions of the Transantarctic Mountains. The last Antarctic glaciation reached a maximum around 18 000 years ago, a period when the present ice sheet was much thicker and extended out to the edge of the continental shelf. The icecaps of offshore islands were similarly more extensive. These extensive ice sheets retreated during the late Pleistocene and have remained relatively stable during the current Holocene epoch. As a result of this temporal evolution, we now see lakes distributed on maritime islands, along the margins of the continent in ablation regions, and subglacially, beneath the thick ice sheet. All these lakes reflect, to varying degrees, the legacy left by past geological and climatological conditions. This article describes the formation, distribution, and diversity of lakes in selected regions in Antarctica where focused research efforts have occurred. Although no subglacial lakes have been sampled directly, we present an overview of what is known about them,with a focus on Lake Vostok, the largest of these lakes.Item Bacteria in subglacial environments(2008) Christner, Brent C.; Skidmore, Mark L.; Priscu, John C.; Tranter, Martyn; Foreman, Christine M.Glaciers exist where the annual temperature remains cold enough to allow snowfall to accumulate for an extended period of time and where conditions allow subsequent metamorphosis to ice. Glacial ice forms expansive continental ice sheets in the polar regions, (e.g., in Antarctica and Greenland), and at lower latitudes, ice fields (valley or alpine glaciers) and ice caps (if a volcano or mountain range is completely glaciated) exist globally at high altitude. Temperate glaciers comprise <4% of the glacial ice on the planet, but are important freshwater reservoirs and are often the sources for major rivers vital for irrigation, industry, and providing millions of people with drinking water. The Greenland and Antarctic ice sheets currently cover ~10% of the terrestrial surface (>1.5×107 km2) and contain ~75% of the freshwater on Earth (Paterson 1994). The Antarctic ice sheet alone contains ~90% of the planet's ice and, if melted, would result in a sea level rise of ~65 m (The National Snow and Ice Data Center; http://nsidc.org/).Item Antarctic subglacial water: Origin, evolution and ecology(2008-09) Priscu, John C.; Tulaczyk, Slawek; Studinger, Michael; Kennicutt II, Mahlon C.; Christner, Brent C.; Foreman, Christine M.Recent discoveries in the polar regions have revealed that subglacial environments provide a habitat for life in a setting that was previously thought to be inhospitable. These habitats consist of large lakes, intermittently flowing rivers, wetlands, and subglacial aquifers. This chapter presents an overview of the geophysical, chemical, and biological properties of selected subglacial environments. The focus is on the large subglacial systems lying beneath Antarctic ice sheets where most of the subglacial water on our planet is thought to exist. Specifically, this chapter addresses the following topics: (1) the distribution, origin, and hydrology of Antarctic subglacial lakes; (2) Antarctic ice streams as regions of dynamic liquid-water movement that influence ice-sheet dynamics; and (3) subglacial environments as habitats for life and reservoirs of organic carbon.Item Redefinition and global estimation of basal ecosystem respiration rate(2001-10-13) Yuan, Wenping; Luo, Yiqi; Li, Shuguang; Yu, Guirui; Zhou, Tao; Bahn, Michael; Black, Andy T.; Desai, Ankur R.; Cescatti, Alessandro; Marcolla, Barbara; Jacobs, Cor; Chen, Jiquan; Aurela, Mika; Bernhofer, Christian; Gielen, Bert; Bohrer, Gil; Cook, David R.; Dragoni, Danilo; Dunn, Allison L.; Gianelle, Damiano; Grünwald, Thomas; Ibrom, Andreas; Leclerc, Monique Y.; Lindroth, Anders; Liu, Heping; Marchesini, Luca Belelli; Montagnani, Leonardo; Pita, Gabriel; Rodeghiero, Mirco; Rodrigues, Abel; Starr, Gregory; Stoy, Paul C.Basal ecosystem respiration rate (BR), the ecosystem respiration rate at a given temperature, is a common and important parameter in empirical models for quantifying ecosystem respiration (ER) globally. Numerous studies have indicated that BR varies in space. However, many empirical ER models still use a global constant BR largely due to the lack of a functional description for BR. In this study, we redefined BR to be ecosystem respiration rate at the mean annual temperature. To test the validity of this concept, we conducted a synthesis analysis using 276 site-years of eddy covariance data, from 79 research sites located at latitudes ranging from ∼3°S to ∼70°N. Results showed that mean annual ER rate closely matches ER rate at mean annual temperature. Incorporation of site-specific BR into global ER model substantially improved simulated ER compared to an invariant BR at all sites. These results confirm that ER at the mean annual temperature can be considered as BR in empirical models. A strong correlation was found between the mean annual ER and mean annual gross primary production (GPP). Consequently, GPP, which is typically more accurately modeled, can be used to estimate BR. A light use efficiency GPP model (i.e., EC-LUE) was applied to estimate global GPP, BR and ER with input data from MERRA (Modern Era Retrospective-Analysis for Research and Applications) and MODIS (Moderate resolution Imaging Spectroradiometer). The global ER was 103 Pg C yr −1, with the highest respiration rate over tropical forests and the lowest value in dry and high-latitude areas.