Magnetotactic bacteria (MTB) synthesize magnetite and greigite crystals under low oxygen conditions in the water column or uppermost sediment (greigite‐producing bacteria are found below the oxic‐anoxic transition). Dissolved iron and oxygen contents in local environments are known to be limiting factors for the production and preservation of biogenic magnetite. Understanding the processes that link MTB to their living environments is fundamental to reconstructing past chemical variations in the water column and sediment, and for using the magnetic properties of biogenic magnetite as environmental proxy indicators. Previous studies have suggested that the frequently identified biogenic soft (BS) and biogenic hard (BH) magnetite types are associated with equant and more elongated morphologies, respectively, and that their abundance varies in accordance with sedimentary oxygen content, where MTB that produce the BH component live in less oxygenated environments. We test this hypothesis in a high‐resolution integrated environmental magnetic and geochemical study of surface sediments from Mamanguá Ría, SE Brazil. Based on magnetic and pore water profiles, we demonstrate that both the BS and BH components occur within microaerobic environments and that as sediment oxygen content decreases with depth, the BS component disappears before the BH component. With continued burial into the sulfidic diagenetic zone, both components undergo progressive dissolution, but the BH component is more resistant to dissolution than the BS component. Our observations confirm previous inferences about the relative stability of these phases and provide a firmer basis for use of these two types of biogenic magnetite as paleoenvironmental proxies.

We performed laboratory experiments to investigate the sensitivity of the Spectral Induced Polarization (SIP) method to toluene contamination in clayey soils. We used mixtures of quartzitic sand and montmorillonite as soil samples, artificially contaminated with varying amounts of toluene. Care was taken to quantify the experimental uncertainty resulting from packing since such effects must be quantified if variations in SIP signatures between samples are to be reliably interpreted in terms of the effects of hydrocarbon concentration. The SIP response of all samples following addition of toluene was monitored for a period of 40 days following sample preparation. Stepwise regression was used to examine the statistical significance of correlations between (i) clay content and (ii) toluene concentration and SIP parameters. Both single‐frequency real and imaginary conductivity measurements, along with the integral chargeability, normalized chargeability, DC conductivity and time constant obtained from a Debye decomposition fitting, were examined in this regression analysis. The SIP measurements show a clear time dependence following sample preparation, indicating that samples containing toluene may take significant time to reach an equilibrium electrical response. SIP measurements are significantly related to toluene content shortly after sample preparation, when the expected dependence of SIP on clay concentration is apparently suppressed. However, for the state of electrical equilibrium after 40 days (interpreted to indicate surface chemistry at equilibrium) there is no significant relation between SIP measurements and toluene content; instead SIP measurements are then significantly correlated with clay concentration. The total chargeability, normalized chargeability and relaxation time obtained from the Debye decomposition show no correlation with toluene content, indicating that this procedure, which likely integrates over multiple mechanisms, may not be suitable for understanding relationships between SIP and hydrocarbon contamination. We find only small low‐frequency polarization signals observed in relation to toluene concentration (2 mrad at 0.01 Hz), which initially decreases the interfacial polarization. Unlike earlier works, our results do not support the use of the SIP method as a tool for monitoring toluene contamination in clay soils.

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Natural attenuation is very often the remediation method of necessity, rather than choice, for beach environments impacted by offshore exploration/drilling accidents. Robust methods that can be efficiently utilized in difficult to access and ecologically sensitive areas are needed for the long-term monitoring of such degradation processes. A prime candidate for such a monitoring tool is the spectral induced polarization (SIP) method, a geophysical technique successfully used for characterization and monitoring of hydrocarbon degradation in freshwater environments. In this laboratory experiment the SIP method successfully monitored the natural degradation of beach sediments impacted by the Deepwater Horizon oil spill. Using the SIP, we were able to differentiate between biotic (e.g., microbial driven) and abiotic (e.g., dilution) degradation processes and infer degradation rates. To our knowledge this is the first effort to use the SIP method as a monitoring aid in high salinity environments.Plain Language Summary Offshore drilling/exploration accidents can result in the contamination of remote and ecologically sensitive areas. In most cases the only realistic remediation choice is natural degradation. In this paper we discuss the use of a noninvasive geophysical method, termed spectral induced polarization, as a monitoring tool of oil contamination degradation in brackish environments. The presented laboratory works supports the suitability of the method for monitoring not only the progress of degradation but also any microbial related degradation processes.

Soil stabilization involves methods used to turn unconsolidated and unstable soil into a stiffer, consolidated medium that could support engineered structures, alter permeability, change subsurface flow, or immobilize contamination through mineral precipitation. Among the variety of available methods carbonate precipitation is a very promising one, especially when it is being induced through common soil borne microbes (MICP - microbial induced carbonate precipitation). Such microbial mediated precipitation has the added benefit of not harming the environment as other methods can be environmentally detrimental. Carbonate precipitation, typically in the form of calcite, is a naturally occurring process that can be manipulated to deliver the expected soil strengthening results or permeability changes. This study investigates the ability of spectral induced polarization and shear-wave velocity for monitoring calcite driven soil strengthening processes. The results support the use of these geophysical methods as soil strengthening characterization and long term monitoring tools, which is a requirement for viable soil stabilization projects. Both tested methods are sensitive to calcite precipitation, with SIP offering additional information related to long term stability of precipitated carbonate. Carbonate precipitation has been confirmed with direct methods, such as direct sampling and scanning electron microscopy (SEM). This study advances our understanding of soil strengthening processes and permeability alterations, and is a crucial step for the use of geophysical methods as monitoring tools in microbial induced soil alterations through carbonate precipitation.