scholarly journals Seasonal variations in pore water and sediment geochemistry of littoral lake sediments (Asylum Lake, MI, USA)

2006 ◽  
Vol 7 (1) ◽  
Author(s):  
Carla M Koretsky ◽  
Johnson R Haas ◽  
Douglas Miller ◽  
Noah T Ndenga
1985 ◽  
Vol 20 (1) ◽  
pp. 106-117 ◽  
Author(s):  
E. Nagy ◽  
D.S. Painter

Abstract A five month survey of 2,4-D in Buckhorn Lake water and sediment, combined with streamflow data, produced estimates of the chemical in the lake. The peak concentrations in the water alone were significantly higher than the documented uses would permit. Two distinct concentration peaks were shown by the chemical: one during the June milfoil control season, and one in late August, indicating a release of 2,4-D from the collapsed and decaying milfoil beds. The observed rates of disappearance of the chemical agreed with reported values, showing a limited persistence in the lake. The presence of 2,4-D in the spring sediments was attributed to land runoff.


Geology ◽  
2020 ◽  
Author(s):  
Netta Shalev ◽  
Tomaso R.R. Bontognali ◽  
Derek Vance

Recent studies have uncovered the potential of Mg isotopes (δ26Mg) for studying past ocean chemistry, but records of such data are still scarce. Dolomite has been suggested as a promising archive for δ26Mg of seawater. However, its enigmatic formation mechanism and the difficulty in precipitating dolomite in the laboratory at surface temperatures decrease confidence in the interpretation of δ26Mg values from the rock record. To evaluate factors determining the δ26Mg of dolomite, we studied pore water and sediment from Dohat Faishakh Sabkha, Qatar—one of the rare environments where dolomite is currently forming. The δ26Mg values of the dolomite (–2.56‰ to –1.46‰) are lower than that of seawater (–0.83‰), whereas δ26Mg values of pore water (–0.71‰ to –0.14‰) are higher. The isotope fractionation accompanying dolomite formation is generally in accordance with an empirical fractionation from the literature, extrapolated to the sabkha’s temperature (–1.84‰ to –1.51‰). The results suggest that evaporated seawater is the sole source of Mg, and isotopically light dolomite is the major sink, so that the δ26Mg of the dolomite-forming pore water is equal to or greater than that of seawater. Thus, provided that the lowest δ26Mg value among several dolomite samples is used, and the formation temperature is known, similar sabkha-type dolomites can be utilized as an archive for δ26Mg values of ancient seawater.


2016 ◽  
Author(s):  
Matthias Egger ◽  
Peter Kraal ◽  
Tom Jilbert ◽  
Fatimah Sulu-Gambari ◽  
Célia J. Sapart ◽  
...  

Abstract. The surface sediments in the Black Sea are underlain by extensive deposits of iron (Fe) oxide-rich lake sediments that were deposited prior to the inflow of marine Mediterranean Sea waters ca. 9000 years ago. The subsequent downward diffusion of marine sulfate into the methane-bearing lake sediments has led to a multitude of diagenetic reactions in the sulfate-methane transition zone (SMTZ), including anaerobic oxidation of methane (AOM) with sulfate. While the sedimentary cycles of sulfur (S), methane and Fe in the SMTZ have been extensively studied, relatively little is known about the diagenetic alterations of the sediment record occurring below the SMTZ. Here we combine detailed geochemical analyses of the sediment and pore water with multicomponent diagenetic modeling to study the diagenetic alterations below the SMTZ at two sites in the western Black Sea. We focus on the dynamics of Fe, S and phosphorus (P) and demonstrate that diagenesis has strongly overprinted the sedimentary burial records of these elements. Our results show that sulfate-mediated AOM substantially enhances the downward diffusive flux of sulfide into the deep limnic deposits. During this downward sulfidization, Fe oxides, Fe carbonates and Fe phosphates (e.g. vivianite) are converted to sulfide phases, leading to an enrichment in solid phase S and the release of phosphate to the pore water. Below the sulfidization front, high concentrations of dissolved ferrous Fe (Fe2+) lead to sequestration of downward diffusing phosphate as authigenic vivianite, resulting in a transient accumulation of total P directly below the sulfidization front. Our model results further demonstrate that downward migrating sulfide becomes partly re-oxidized to sulfate due to reactions with oxidized Fe minerals, fueling a cryptic S cycle and thus stimulating slow rates of sulfate-driven AOM (~ 1–100 pmol cm−3 d−1) in the sulfate-depleted limnic deposits. However, this process is unlikely to explain the observed release of dissolved Fe2+ below the SMTZ. Instead, we suggest that besides organoclastic Fe oxide reduction, AOM coupled to the reduction of Fe oxides may also provide a possible mechanism for the high concentrations of Fe2+ in the pore water at depth. Our results reveal that methane plays a key role in the diagenetic alterations of Fe, S and P records in Black Sea sediments. The downward sulfidization into the limnic deposits is enhanced through sulfate-driven AOM with sulfate and AOM with Fe oxides may provide a deep source of dissolved Fe2+ that drives the sequestration of P in vivianite below the sulfidization front.


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