Geology topics

T. Barkay

Publications and source records attributed to T. Barkay.

5 recordsLinked to original sources

USGS2011

Environmental conditions constrain the distribution and diversity of archaeal merA in Yellowstone National Park, Wyoming, U.S.A.

The distribution and phylogeny of extant protein-encoding genes recovered from geochemically diverse environments can provide insight into the physical and chemical parameters that led to the origin and which constrained the evolution of a functional process. Mercuric reductase (MerA) plays an integral role in mercury (Hg) biogeochemistry by catalyzing the transformation of Hg(II) to Hg(0). Putative merA sequences were amplified from DNA extracts of microbial communities associated with mats and sulfur precipitates from physicochemically diverse Hg-containing springs in Yellowstone National Park, Wyoming, using four PCR primer sets that were designed to capture the known diversity of merA. The recovery of novel and deeply rooted MerA lineages from these habitats supports previous evidence that indicates merA originated in a thermophilic environment. Generalized linear models indicate that the distribution of putative archaeal merA lineages was constrained by a combination of pH, dissolved organic carbon, dissolved total mercury and sulfide. The models failed to identify statistically well supported trends for the distribution of putative bacterial merA lineages as a function of these or other measured environmental variables, suggesting that these lineages were either influenced by environmental parameters not considered in the present study, or the bacterial primer sets were designed to target too broad of a class of genes which may have responded differently to environmental stimuli. The widespread occurrence of merA in the geothermal environments implies a prominent role for Hg detoxification in these environments. Moreover, the differences in the distribution of the merA genes amplified with the four merA primer sets suggests that the organisms putatively engaged in this activity have evolved to occupy different ecological niches within the geothermal gradient.

Yellowstone National Park↗

USGS2009

Mercury isotopic composition of hydrothermal systems in the Yellowstone Plateau volcanic field and Guaymas Basin sea-floor rift

To characterize mercury (Hg) isotopes and isotopic fractionation in hydrothermal systems we analyzed fluid and precipitate samples from hot springs in the Yellowstone Plateau volcanic field and vent chimney samples from the Guaymas Basin sea-floor rift. These samples provide an initial indication of the variability in Hg isotopic composition among marine and continental hydrothermal systems that are controlled predominantly by mantle-derived magmas. Fluid samples from Ojo Caliente hot spring in Yellowstone range in δ 202 Hg from - 1.02&permil; to 0.58&permil; (± 0.11&permil;, 2SD) and solid precipitate samples from Guaymas Basin range in δ 202 Hg from - 0.37&permil; to - 0.01&permil; (± 0.14&permil;, 2SD). Fluid samples from Ojo Caliente display mass-dependent fractionation (MDF) of Hg from the vent (δ 202 Hg = 0.10&permil; ± 0.11&permil;, 2SD) to the end of the outflow channel (&delta 202 Hg = 0.58&permil; ± 0.11&permil;, 2SD) in conjunction with a decrease in Hg concentration from 46.6pg/g to 20.0pg/g. Although a small amount of Hg is lost from the fluids due to co-precipitation with siliceous sinter, we infer that the majority of the observed MDF and Hg loss from waters in Ojo Caliente is due to volatilization of Hg 0 (aq) to Hg 0 (g) and the preferential loss of Hg with a lower δ 202 Hg value to the atmosphere. A small amount of mass-independent fractionation (MIF) was observed in all samples from Ojo Caliente (Δ 199 Hg = 0.13&permil; ±1 0.06&permil;, 2SD) but no significant MIF was measured in the sea-floor rift samples from Guaymas Basin. This study demonstrates that several different hydrothermal processes fractionate Hg isotopes and that Hg isotopes may be used to better understand these processes.

Wyoming↗

USGS2009

Methylmercury enters an aquatic food web through acidophilic microbial mats in Yellowstone National Park, Wyoming

Microbial mats are a visible and abundant life form inhabiting the extreme environments in Yellowstone National Park (YNP), WY, USA. Little is known of their role in food webs that exist in the Park's geothermal habitats. Eukaryotic green algae associated with a phototrophic green/purple Zygogonium microbial mat community that inhabits low-temperature regions of acidic (pH ∼ 3.0) thermal springs were found to serve as a food source for stratiomyid (Diptera: Stratiomyidae) larvae. Mercury in spring source water was taken up and concentrated by the mat biomass. Monomethylmercury compounds (MeHg + ), while undetectable or near the detection limit (0.025 ng l −1 ) in the source water of the springs, was present at concentrations of 4–7 ng g −1 dry weight of mat biomass. Detection of MeHg + in tracheal tissue of larvae grazing the mat suggests that MeHg + enters this geothermal food web through the phototrophic microbial mat community. The concentration of MeHg + was two to five times higher in larval tissue than mat biomass indicating MeHg + biomagnification occurred between primary producer and primary consumer trophic levels. The Zygogonium mat community and stratiomyid larvae may also play a role in the transfer of MeHg + to species in the food web whose range extends beyond a particular geothermal feature of YNP.

Wyoming↗

USGS2000

Mercury biogeochemistry in the Idrija River, Slovenia, from above the mine into the Gulf of Trieste

The Idrija Mine is the second largest Hg mine in the world which operated for 500 years. Mercury (Hg)-laden tailings still line the banks, and the system is a threat to the Idrija River and water bodies downstream including the Soca/Isonzo River and the Gulf of Trieste in the northern Adriatic Sea. A multidisciplinary study was conducted in June 1998 on water samples collected throughout the Idrija and Soca River systems and waters and sediments in the Gulf. Total Hg in the Idrija River increased >20-fold downstream of the mine from <3 to >60 ng liter-1 with methyl mercury (MeHg) accounting for ~0.5%. Concentrations increased again downstream and into the estuary with MeHg accounting for nearly 1.5% of the total. While bacteria upstream of the mine did not contain mercury detoxification genes (mer), such genes were detected in bacteria collected downstream. Benthic macroinvertebrate diversity decreased downstream of the mine. Gulf waters near the river mouth contained up to 65 ng liter-1 total Hg with ~0.05 ng liter-1 MeHg. Gulf sediments near the river mouth contained 40 ??g g-1 total Hg with MeHg concentrations of about 3 ng g-1. Hg in sediment pore waters varied between 1 and 8 ng liter-1, with MeHg accounting for up to 85%. Hg methylation and MeHg demethylation were active in Gulf sediments with highest activities near the surface. MeHg was degraded by an oxidative pathway with >97% C released from MeHg as CO2. Hg methylation depth profiles resembled profiles of dissolved MeHg. Hg-laden waters still strongly impact the riverine, estuarine, and marine systems. Macroinvertebrates and bacteria in the Idrija River responded to Hg stress, and high Hg levels persist into the Gulf. Increases in total Hg and MeHg in the estuary demonstrate the remobilization of Hg, presumably as HgS dissolution and recycling. Gulf sediments actively produce MeHg, which enters bottom waters and presumably the marine food chain. (C) 2000 Academic Press.

Conference Paper↗

USGS1995

Methylmercury oxidative degradation potentials in contaminated and pristine sediments of the Carson River, Nevada

Sediments from mercury-contaminated and uncontaminated reaches of the Carson River, Nevada, were assayed for sulfate reduction, methanogenesis, denitrification, and monomethylmercury (MeHg) degradation. Demethylation of [ 14 C]MeHg was detected at all sites as indicated by the formation of 14 CO 2 and 14 CH 4 . Oxidative demethylation was indicated by the formation of 14 CO 2 and was present at significant levels in all samples. Oxidized/reduced demethylation product ratios (i.e., 14 CO 2 / 14 CH 4 ratios) generally ranged from 4.0 in surface layers to as low as 0.5 at depth. Production of 14 CO 2 was most pronounced at sediment surfaces which were zones of active denitrification and sulfate reduction but was also significant within zones of methanogenesis. In a core taken from an uncontaminated site having a high proportion of oxidized, coarse-grain sediments, sulfate reduction and methanogenic activity levels were very low and 14 CO 2 accounted for 98% of the product formed from [ 14 C]MeHg. There was no apparent relationship between the degree of mercury contamination of the sediments and the occurrence of oxidative demethylation. However, sediments from Fort Churchill, the most contaminated site, were most active in terms of demethylation potentials. Inhibition of sulfate reduction with molybdate resulted in significantly depressed oxidized/reduced demethylation product ratios, but overall demethylation rates of inhibited and uninhibited samples were comparable. Addition of sulfate to sediment slurries stimulated production of 14 CO 2 from [ 14 C]MeHg, while 2-bromoethanesulfonic acid blocked production of 14 CH 4 . These results reveal the importance of sulfate-reducing and methanogenic bacteria in oxidative demethylation of MeHg in anoxic environments.

Nevada↗