Geology topics

M.E. Berndt

Publications and source records attributed to M.E. Berndt.

3 recordsLinked to original sources

USGS2016

Aeshnid dragonfly larvae as bioindicators of methylmercury contamination in aquatic systems impacted by elevated sulfate loading

Methylmercury (MeHg) levels in dragonfly larvae and water were measured over two years in aquatic systems impacted to varying degrees by sulfate releases related to iron mining activity. This study examined the impact of elevated sulfate loads on MeHg concentrations and tested the use of MeHg in dragonfly larvae as an indicator of MeHg levels in a range of aquatic systems including 16 river/stream sites and two lakes. MeHg concentrations in aeshnid dragonfly larvae were positively correlated ( R 2 = 0.46, p < 0.01) to peak MeHg concentrations in the dissolved phase for the combined years of 2012 and 2013. This relation was strong in 2012 ( R 2 = 0.85, p < 0.01), but showed no correlation in 2013 ( R 2 = 0.02, p > 0.05). MeHg in dragonfly larvae were not elevated at the highest sulfate sites, but rather the reverse was generally observed. Record rainfall events in 2012 and above average rainfall in 2013 likely delivered the majority of Hg and MeHg to these systems via interflow and activated groundwater flow through reduced sediments. As a result, the impacts of elevated sulfate releases due to mining activities were not apparent in these systems where little of the sulfate is reduced. Lower bioaccumulation factors for MeHg in aeshnid dragonfly larvae were observed with increasing dissolved organic carbon (DOC) concentrations. This finding is consistent with previous studies showing that MeHg in high DOC systems is less bioavailable; an equilibrium model shows that more MeHg being associated with DOC rather than algae at the base of the food chain readily explains the lower bioaccumulation factors.

Ecotoxicology↗

USGS2012

Mineralogy and geochemistry of a sediment‐hosted hydrothermal sulfide deposit from the Southern Trough of Guaymas Basin, Gulf of California

Samples dredged from a 15‐m‐high hydrothermal mound atop the flat turbidite pond in the Southern Trough of Guaymas Basin consist of pyrrhotite‐rich massive sulfide, barite, barite + calcite, talc, and opaline silica as well as substrate material composed of fossiliferous, clay‐rich ooze. An 11‐m‐long sediment core taken near the dredge site shows increasing hydrothermal alteration with depth; anhydrite‐filled fractures near the base of the core appear to be channels for hydrothermal discharge. Oxidation of the sulfide‐rich samples to an assemblage of geothite, lepidocrocite, and amorphous Fe oxyhydroxide is ubiquitous. Compared to other massive sulfide deposits on sediment‐starved oceanic ridges, the hydrothermal deposit dredged in Guaymas Basin has a high pyrrhotite/pyrite ratio, a low Zn sulfide and combined ore metal (Cu + Zn + Pb + Ag + Cd) content, and a greater abundance of sulfate, carbonate, and silicate phases. Venting hydrothermal solutions are alkaline with moderately high p H; high Ca, Ba, and SiO 2 content; low ƒS 2 and ƒo 2 ; and very low transition metal content. Disequilibrium assemblages of pyrrhotite and sulfate minerals form during rapid mixing of this evolved vent fluid with ambient bottom waters at the discharge site. Talc is formed at a temperature near 270°C by mixing or entrainment of Mg‐rich bottom water or pore fluid with upwelling hydrothermal fluid that is saturated with silica. Calcite may precipitate from the alkaline, Ca‐rich fluid during degassing of CO 2 . The minimum temperature range for sulfide and nonsulfide deposition is approximately 190°–326°C. The composition of hydrothermal deposits, vent solutions, and altered sediment requires that circulating fluids evolve during deep penetration into the basaltic basement complex, further interaction with the organic‐and carbonate‐rich sediment pile, and near‐surface mixing with ambient seawater. Although the stable assemblage albite‐epidote‐clinochlore present at depth in the sediment pile requires very low dissolved Mg and Fe in the altering fluid, the addition of Mg to deeply buried sediment indicates significant recharge of the system by Guaymas Basin bottom water.

Southern Trough of Guaymas Basin↗

USGS1996

Hydrogen isotope systematics of phase separation in submarine hydrothermal systems: Experimental calibration and theoretical models

Hydrogen isotope fractionation factors were measured for coexisting brines and vapors formed by phase separation of NaCl/H2O fluids at temperatures ranging from 399-450??C and pressures from 277-397 bars. It was found that brines are depleted in D compared to coexisting vapors at all conditions studied. The magnitude of hydrogen isotope fractionation is dependent on the relative amounts of Cl in the two phases and can be empirically correlated to pressure using the following relationship: 1000 ln ??(vap-brine) = 2.54(??0.83) + 2.87(??0.69) x log (??P), where ??(vap-brine) is the fractionation factor and ??P is a pressure term representing distance from the critical curve in the NaCl/H2O system. The effect of phase separation on hydrogen isotope distribution in subseafloor hydrothermal systems depends on a number of factors, including whether phase separation is induced by heating at depth or by decompression of hydrothermal fluids ascending to the seafloor. Phase separation in most subseafloor systems appears to be a simple process driven by heating of seawater to conditions within the two-phase region, followed by segregation and entrainment of brine or vapor into a seawater dominated system. Resulting vent fluids exhibit large ranges in Cl concentration with no measurable effect on ??D. Possible exceptions to this include hydrothermal fluids venting at Axial and 9??N on the East Pacific Rise. High ??D values of low Cl fluids venting at Axial are consistent with phase separation taking place at relatively shallow levels in the oceanic crust while negative ??D values in some low Cl fluids venting at 9??N suggest involvement of a magmatic fluid component or phase separation of D-depleted brines derived during previous hydrothermal activity.

Geochimica et Cosmochimica Acta↗