Increase In Redox Potential Research Articles

Characteristics and Causes of High-manganese Groundwater in Pearl River Delta During Urbanization

The high concentration of iron and manganese in groundwater is harmful to human health, and the sources of manganese in rapidly urbanization areas are complex. Based on more than 2500 sets of hydrochemical data in different historical periods, the spatial distribution characteristics, sources, and genesis of groundwater manganese in different aquifers and areas with different urbanization levels in the Pearl River Delta were studied by using mathematical statistics and principal component analysis. The results showed that the concentration of manganese in groundwater in the pore aquifer was obviously higher than that in the fissure and karst aquifer. The proportion of high-manganese groundwater in the pore aquifer was twice that in the fissure and karst aquifer. The proportion of high-manganese groundwater in urbanized and suburban areas was significantly higher than that in non-urbanized areas. On a regional scale, the decomposition of organic matter and the reductive dissolution of Fe-Mn (oxygen) hydroxide in sedimentary strata under reductive conditions may have been the main factors controlling the increase in manganese concentration in pore aquifers. High-manganese groundwater in fissured aquifers may have been affected by low-oxygen domestic sewage leakage accompanying urbanization and industrial wastewater leakage and infiltration accompanying industrialization. The pore high-manganese groundwater was controlled by reduction conditions, and the weakly acidic environment of fissure and karst high-manganese groundwater was the important influencing factor. In the past 10 years, the groundwater environment in the study area has been improving, and the increase in groundwater redox potential and pH was not conducive to the formation of high-manganese groundwater, which was also the main cause of the overall decrease in Mn2+ concentration in groundwater of different types of aquifers in the process of urbanization.

Electron acceptors determine the BTEX degradation capacity of anaerobic microbiota via regulating the microbial community

Anaerobic degradation is the major pathway for microbial degradation of benzene, toluene, ethylbenzene, and xylenes (BTEX) under electron acceptor lacking conditions. However, how exogenous electron acceptors modulate BTEX degradation through shaping the microbial community structure remains poorly understood. Here, we investigated the effect of various exogenous electron acceptors on BTEX degradation as well as methane production in anaerobic microbiota, which were enriched from the same contaminated soil. It was found that the BTEX degradation capacities of the anaerobic microbiota gradually increased along with the increasing redox potentials of the exogenous electron acceptors supplemented (WE: Without exogenous electron acceptors < SS: Sulfate supplement < FS: Ferric iron supplement < NS: Nitrate supplement), while the complexity of the co-occurring networks (e.g., avgK and links) of the microbiota gradually decreased, showing that microbiota supplemented with higher redox potential electron acceptors were less dependent on the formation of complex microbial interactions to perform BTEX degradation. Microbiota NS showed the highest degrading capacity and the broadest substrate-spectrum for BTEX, and it could metabolize BTEX through multiple modules which not only contained fewer species but also different key microbial taxa (eg. Petrimonas, Achromobacter and Comamonas). Microbiota WE and FS, with the highest methanogenic capacities, shared common core species such as Sedimentibacter, Acetobacterium, Methanobacterium and Smithella/Syntrophus, which cooperated with Geobacter (microbiota WE) or Desulfoprunum (microbiota FS) to perform BTEX degradation and methane production. This study demonstrates that electron acceptors may alter microbial function by reshaping microbial community structure and regulating microbial interactions and provides guidelines for electron acceptor selection for bioremediation of aromatic pollutant-contaminated anaerobic sites.

Control of redox potential in a novel continuous bioelectrochemical system led to remarkable metabolic and energetic responses of Clostridium pasteurianum grown on glycerol

BackgroundElectro-fermentation (EF) is an emerging tool for bioprocess intensification. Benefits are especially expected for bioprocesses in which the cells are enabled to exchange electrons with electrode surfaces directly. It has also been demonstrated that the use of electrical energy in BES can increase bioprocess performance by indirect secondary effects. In this case, the electricity is used to alter process parameters and indirectly activate desired pathways. In many bioprocesses, oxidation-reduction potential (ORP) is a crucial process parameter. While C. pasteurianum fermentation of glycerol has been shown to be significantly influenced electrochemically, the underlying mechanisms are not clear. To this end, we developed a system for the electrochemical control of ORP in continuous culture to quantitatively study the effects of ORP alteration on C. pasteurianum by metabolic flux analysis (MFA), targeted metabolomics, sensitivity and regulation analysis.ResultsIn the ORP range of −462 mV to −250 mV, the developed algorithm enabled a stable anodic electrochemical control of ORP at desired set-points and a fixed dilution rate of 0.1 h−1. An overall increase of 57% in the molar yield for 1,3-propanediol was observed by an ORP increase from −462 to −250 mV. MFA suggests that C. pasteurianum possesses and uses cellular energy generation mechanisms in addition to substrate-level phosphorylation. The sensitivity analysis showed that ORP exerted its strongest impact on the reaction of pyruvate-ferredoxin-oxidoreductase. The regulation analysis revealed that this influence is mainly of a direct nature. Hence, the observed metabolic shifts are primarily caused by direct inhibition of the enzyme upon electrochemical production of oxygen. A similar effect was observed for the enzyme pyruvate-formate-lyase at elevated ORP levels.ConclusionsThe results show that electrochemical ORP alteration is a suitable tool to steer the metabolism of C. pasteurianum and increase product yield for 1,3-propanediol in continuous culture. The approach might also be useful for application with further anaerobic or anoxic bioprocesses. However, to maximize the technique's efficiency, it is essential to understand the chemistry behind the ORP change and how the microbial system responds to it by transmitted or direct effects.

Attempts to Stimulate Leaching Activity of Acidithiobacillus ferrooxidans Strain TFBk

Autotrophic acidophilic bacteria Acidithiobacillus ferrooxidans is a model species for studying metal bioleaching from low-grade sulfide ores and concentrates. Arsenopyrite gold-bearing concentrates are refractory and often processed using biohydrometallurgical approaches; therefore, it is important to develop methods to improve arsenopyrite bioleaching. In the present work, we have studied the possibility of improving arsenopyrite concentrate bioleaching by the strain of A. ferrooxidans. For this purpose, we have analyzed the genome of the strain A. ferrooxidans TFBk to reveal the genes potentially important in the bioleaching process. Genes determining resistance to arsenic, as well genes involved in the utilization of C1-compounds and resistance to oxidative stress, were revealed. Therefore, the possibility of increasing the rate of arsenopyrite concentrate bioleaching using C1-compounds (methanol and formate) was studied. Formate was able to increase both the biomass yield of the strain A. ferrooxidans TFBk as well as the bioleaching rate. In addition, the effect of redox potential increase by means of the addition of sodium persulfate in the medium on arsenopyrite concentrate bioleaching was studied. It was shown that the addition of 0.1% sodium persulfate stimulated strain growth, while a higher concentration inhibited it. Despite this, the rate of concentrate bioleaching increased in the presence of 0.5–1.0% of persulfate, which may be explained by the interactions of added oxidizer with concentrate components.

L. monocytogens exhibited less cell membrane damage, lipid peroxidation, and intracellular reactive oxygen species accumulation after plasma-activated water treatment compared to E. coli O157:H7 and S. Typhimurium

This study investigated the bactericidal activity of plasma-activated water (PAW) generated with a remote discharge reactor against Escherichia coli O157:H7, Salmonella Typhimurium, and Listeria monocytogenes. PAW-40, -80, and −120, prepared by activating distilled water for 40, 80, and 120 min, respectively, showed inactivation activity against pathogenic bacteria, which increased as the activation time increased due to decrease in pH and increase in oxidation-reduction potential and reactive oxygen/nitrogen species (RONS) of PAW. In addition, Gram-positive bacteria L. monocytogenes showed superior resistance to PAW than Gram-negative bacteria E. coli O157:H7 and S. Typhimurium. Compared with E. coli O157:H7 and S. Typhimurium, L. monocytogens exhibited less cell membrane damage, lipid peroxidation, and intracellular ROS accumulation after PAW treatment, which indicated that L. monocytogenes exhibited greater resistance because the thick cell wall buffered RONS diffusion into the cell. PAW also showed a control effect on the pathogenic bacteria on cherry tomato, and the effect was maintained throughout five repeated applications; thus, proposing high reusability of PAW. The results of this study propose that PAW generated with a remote discharge reactor can be utilized for pathogen control and provides basic data for related research and practical industrial applications.

Sulfur-driven methylmercury production in paddies continues following soil oxidation

Methylmercury (MeHg) production in paddy soils and its accumulation in rice raise global concerns since rice consumption has been identified as an important pathway of human exposure to MeHg. Sulfur (S) amendment via fertilization has been reported to facilitate Hg methylation in paddy soils under anaerobic conditions, while the dynamic of S-amendment induced MeHg production in soils with increasing redox potential remains unclear. This critical gap hinders a comprehensive understanding of Hg biogeochemistry in rice paddy system which is characterized by the fluctuation of redox potential. Here, we conducted soil incubation experiments to explore MeHg production in slow-oxidizing paddy soils amended with different species of S and doses of sulfate. Results show that the elevated redox potential (1) increased MeHg concentrations by 10.9%−35.2%, which were mainly attributed to the re-oxidation of other S species to sulfate and thus the elevated abundance of sulfate-reducing bacteria, and (2) increased MeHg phytoavailability by up to 75% due to the reductions in acid volatile sulfide (AVS) that strongly binds MeHg in soils. Results obtained from this study call for attention to the increased MeHg production and phytoavailability in paddy soils under elevated redox potentials due to water management, which might aggravate the MeHg production induced by S fertilization and thus enhance MeHg accumulation in rice.

Separating selenium species by diffusion in Brazilian bentonite: a mathematical modeling approach

Bentonite was applied in diffusive studies for selenium, an emerging contaminant. The planar source method was used to determine the apparent and effective diffusion coefficients and assess the mobility of the selenium species. A double Gaussian function described the results. Different diffusion coefficients were associated with different mobilities, and consequently, to the coexistence of two selenium species: selenite and selenate. Apparent diffusion coefficients were higher for selenate, around 10- 10 m2 s- 1, than for selenite, around 10- 12 m2 s- 1. Results from sequential extraction and distribution coefficient justified selenate's greater mobility than selenite. Since the increase in redox potential from 448 to 511 mV may be associated with selenite oxidation in an interconversion process, the diffusion in bentonite demonstrates that applications in geological barriers deserve attention regarding the mobilization of selenium species. Interconversions can mobilize selenium, as reduced species can shift to more oxidized and mobile species, enhancing environmental contamination.

Comparison of continuous and pulse mode of operation of pilot biosand reactors treating winery effluent

In 2020 there was approximately 260 million hectolitres of wine produced across the world. Many winemaking and cellar cleaning activities generate winery wastewater. In vine growing areas which are water stressed, this wastewater is often used for irrigation and if it is inadequately treated it can be detrimental to land and aquatic environments. It has been shown at pilot scale that horizontal flow biosand filters are suitable for treating winery effluent to comply with irrigation standards. In this two-year study, vertical flow biosand reactors with novel design features were operated in both continuous and pulse modes of operation. It was envisaged that (i) the loading rates (organic and hydraulic) could be increased by changing the flow from horizontal to vertical flow, and that (ii) higher organic biodegradation rates could be achieved consequent to the increased redox potential from draw-down of atmospheric oxygen during system drainage in pulse mode in comparison to continuous mode. It was found that system performance was higher in continuous mode, attaining a hydraulic loading rate of 113 L.m−3 of sand a day−1, organic loading rate of 279 gCOD.m−3 of sand.day−1 and COD removal efficiency of 70% compared to pulse mode with 90 L.m−3 of sand a day−1, 192 gCOD.m−3 of sand.day−1 and 70%, respectively. In comparison to other passive winery wastewater treatment systems (constructed/treatment wetlands), these biosand filters are able to treat winery wastewater at higher loading rates with smaller spatial footprints.

Tetrahedral Keggin Core Tunes the Visible Light-Assisted Catalase-Like Activity of Icosahedral Keplerate Shell.

In this work, the effect of Keggin polyoxometalates encapsulated in Keplerate {Mo72Fe30} shell (K shell) on the visible light-assisted catalase-like activity (H2O2 dismutation) of the resulting core-shell clusters PMo12@K, SiMo12@K, and BW12@K was investigated. Superior photodismutation activity of PMo12@K compared to that of K shell and two other core-shell clusters was discovered. The homogeneity of PMo12@K and its improved oxidative stability, increased redox potential, and reduced band gap caused by a synergistic effect between the Keplerate shell and Keggin core seem reasonable to explain such a superiority. The light-dependent photocatalytic performance of PMo12@K evaluated by action spectra revealed a maximum apparent quantum efficiency (AQY) at 400 nm, demonstrating the visible light-driven photocatalytic reaction. A first-order rate constant of 2 × 10-4 s-1 and activation energy of 108.8 kJ mol-1 alongside a turnover frequency of 0.036 s-1 and a total turnover number of up to ∼3800 approved the effective photocatalytic activity and improved the oxidative stability of PMo12@K. A nonradical photocatalytic mechanism through a Fe-OOH intermediate was proposed. Thus, the structure, optical activity, and oxidative stability of a host Keplerate-type nanocluster can be tuned significantly by encapsulation of a guest, like "cluster-in-cluster" structures, which opens the scope for introducing new visible light-sensitive hierarchical nanostructures.

Oxygen Reduction Reaction with Manganese Oxide Nanospheres in Microbial Fuel Cells.

Operating microbial fuel cells (MFCs) under extreme pH conditions offers a substantial benefit. Acidic conditions suppress the growth of undesirable methanogens and increase redox potential for oxygen reduction reactions (ORRs), and alkaline conditions increase the electrocatalytic activity. However, operating any fuel cells, including MFCs, is difficult under such extreme pH conditions. Here, we demonstrate a pH-universal ORR ink based on hollow nanospheres of manganese oxide (h-Mn3O4) anchored with multiwalled carbon nanotubes (MWCNTs) on planar and porous forms of carbon electrodes in MFCs (pH = 3–11). Nanospheres of h-Mn3O4 (diameter ∼ 31 nm, shell thickness ∼ 7 nm) on a glassy carbon electrode yielded a highly reproducible ORR activity at pH 3 and 10, based on rotating disk electrode (RDE) tests. A phenomenal ORR performance and long-term stability (∼106 days) of the ink were also observed with four different porous cathodes (carbon cloth, carbon nanofoam paper, reticulated vitreous carbon, and graphite felt) in MFCs. The ink reduced the charge transfer resistance (Rct) to the ORR by 100-fold and 45-fold under the alkaline and acidic conditions, respectively. The current study promotes ORR activity and subsequently the MFC operations under a wide range of pH conditions, including acidic and basic conditions.

Interactions of Vallisneria natans and Iron-Oxidizing Bacteria Enhance Iron-Bound Phosphorus Formation in Eutrophic Lake Sediments.

Submerged macrophyte restoration and in situ phosphorus (P) passivation are effective methods for the control of internal P loading from sediments. This study explored the synergistic effects of Vallisneria natans and iron (Fe)-oxidizing bacteria (IOB) on internal P loading from eutrophic freshwater lake sediments by taking into account Fe-bound P (FeP) formation and associated bacterial community structures. Sediment samples were prepared in glass tanks under four treatments, namely no V. natans planting or IOB inoculation (control), planting V. natans without IOB inoculation (Va), planting V. natans with IOB inoculation (Va-IOB), and planting V. natans with autoclaved IOB inoculation (Va-IOB[A]). Compared with the control, all three treatments with V. natans (Va, Va-IOB, and Va-IOB[A]) had significantly decreased organic matter contents and increased redox potential in sediments (p < 0.05), at the rapid growth and mature stages of V. natans. Planting V. natans with and without IOB inoculation also decreased the total P (TP) and Fe–P concentrations in sediments. Conversely, Fe3+ concentrations, Fe3+/Fe2+ ratios, and the proportions of Fe–P in TP all increased in sediments planted with V. natans, especially under the Va-IOB treatment (p < 0.05). Furthermore, bacterial community diversity increased in sediments due to the presence of V. natans. The relative abundances of IOB (including Acidovorax and Chlorobium) increased from the transplanting to the rapid growth stage of V. natans and then decreased afterwards. In the later stages, the relative abundances of IOB and their ratios to Fe-reducing bacteria were the highest under the Va-IOB treatment. Accordingly, synergistic interactions between V. natans and IOB could enhance Fe–P formation and reduce TP concentrations in eutrophic lake sediments by altering sediment physicochemical properties and Fe oxidation-related bacterial community structures.

Tuning the Photocatalytic Activity of Tin Oxide Through Mechanical Surface Activation

Tin oxide (SnO2) nanoparticles were synthesized by the co-precipitation method and mechanically modified by high-energy ball milling. The experimental results demonstrate that the collision with zirconia balls produces slight changes in the crystalline, electronic, morphological, and surface properties of SnO2, which lead to an increase in the redox potential of the energy level and the formation of the hydroxyl group on the SnO2 surface. Moreover, these changes are intensified over the milling up to 90 min, directly affecting the photocatalytic performance, which was monitored by the rate of rhodamine B (RhB) degradation driven by ultraviolet (UV) irradiation. As a result, all ground samples showed better photocatalytic activity than pristine SnO2 (Sn-cop). The maximum degradation of rhodamine B was ca. 75%, achieved with 90 min-milled SnO2 nanoparticles (Sn-M90), compared to the Sn-cop sample induced a 1.67 times higher degradation rate. The reaction mechanism suggests that its better photocatalytic activity may be associated with the higher increased redox potential of the valence and conduction bands and the formation of hydroxyl active sites on the catalyst surface principal oxidizing agent generated. Therefore, we conclude that the ball milling process is an efficient way to induce stable activation of oxide metal for photocatalytic applications.

High performance Li-, Na-, and K-ion storage in electrically conducting coordination polymers.

Coordination polymers (CPs) made of redox-active organic moieties and metal ions emerge as an important class of electroactive materials for battery applications. However, the design and synthesis of high voltage alkali-cation reservoir anionic CPs remains challenging, hindering their practical applications. Herein, we report a family of electrically conducting alkali-cation reservoir CPs with the general formula of A2-TM-PTtSA (wherein A = Li+, Na+, or K+; TM = Fe2+, Co2+, or Mn2+; and PTtSA = benzene-1,2,4,5-tetra-methylsulfonamide). The incorporation of transition metal centers not only enables intrinsic high electrical conductivity, but also shows an impressive redox potential increase of as high as 1 V as compared to A4-PTtSA analogues, resulting in a class of organometallic cathode materials with a high average redox potential of 2.95–3.25 V for Li-, Na- and K-ion batteries. A detailed structure – composition – physicochemical properties – performance correlation study is provided relying on experimental and computational analysis. The best performing candidate shows excellent rate capability (86% of the nominal capacity retained at 10C rate), remarkable cycling stability (96.5% after 1000 cycles), outstanding tolerance to low carbon content (5 wt%), high mass loading (50 mg cm−2), and extreme utilisation conditions of low earth orbit space environment tests. The significance of the disclosed alkali-ion reservoir cathodes is further emphasized by utilizing conventional Li-host graphite anode for full cell assembly, attaining a record voltage of 3 V in an organic cathode Li-ion proof-of-concept cell.

Transport and partitioning of metals in river networks of a plain area with sedimentary resuspension and implications for downstream lakes

This study showed that metal transport and partitioning are primarily controlled by suspended solids with seasonal flow regimes in plain river networks with sedimentary resuspension. Eight metal species containing iron (Fe), manganese (Mn), cadmium (Cd), chrome (Cr), copper (Cu), nickel (Ni), lead (Pb), and zinc (Zn), in multiple phases of sediments, suspended solids (>0.7 μm), colloids (1 nm-0.7 μm) and dissolved phase (<1 nm) were analysed to characterize their temporal-spatial patterns, partitioning and transport on a watershed scale. Metal concentrations were associated with suspended solids in the water column and decreased from low flow to high flow. However, metal partitioning between particulate phase (suspended solids) and dissolvable phases (colloids and dissolved phase) was reversed and increased from low flow to high flow with decreased concentration of total suspended solids and median particle size. Partition coefficients (kp) showed differences among metal species, with higher values for Pb (354.3–649.0 L/g) and Cr (54.2–223.7 L/g) and lower values for Zn (2.5–25.2 L/g) and Cd (17.3–21.0 L/g). Metal concentrations in sediments increased by factors of 1.2–3.0 from upstream to downstream in watersheds impacted by urbanization. The behaviours of metals in rivers provide deeper insight into the ecological risks they pose for downstream lakes, where increased redox potential and organic matter may increase metal mobility due to algal blooms. Areas with heavy pollution of metals and the transport routines of metals in the river networks were also revealed in our research.

Plasma activated water prepared by different plasma sources: physicochemical properties and decontamination effect on lentils sprouts

The pulsed corona discharge (CD) generated in contact with water and directly in water, and high-power air plasma jet (APJ) were studied for production of plasma activated water (PAW). The changes of physical (pH, redox potential, conductivity, temperature) and chemical (peroxides, nitrites, nitrates concentrations) properties of treated water were investigated. The comparison of CD generated in gas/water interface and underwater configuration in the same system showed that the interaction of reactive oxygen and nitrogen species formed in ambient air in gas/water system induces different chemical processes, leading to lower pH, higher oxidation-reduction potential (ORP) and higher conductivity of PAW than in underwater discharge. High yield of peroxide was observed in both configurations. The PAW prepared by APJ exhibits high concentration of nitrites and nitrates according to supplied energy, and related significant decrease of pH and increase of ORP and conductivity after treatment. The antimicrobial effect of PAW prepared by CD and plasma jet on lentils sprouts was studied in different treatment and washing times. The APJ appears to have great efficacy on water activation resulted in strong decontamination effect. The PAW treated by APJ for 10 min led to bacterial reduction from initial 8.3 to 5.9 and 4.0 log10 CFU g−1 after 10 and 30 min of washing, respectively.

Divergent responses of wetland methane emissions to elevated atmospheric CO2 dependent on water table

Elevated atmospheric CO2 may have consequences for methane (CH4) emissions from wetlands, yet the magnitude and direction remain unpredictable, because the associated mechanisms have not been fully investigated. Here, we established an in situ macrocosm experiment to compare the effects of elevated CO2 (700 ppm) on the CH4 emissions from two wetlands: an intermittently inundated Calamagrostis angustifolia marsh and a permanently inundated Carex lasiocarpa marsh. The elevated CO2 increased CH4 emissions by 27.6–57.6% in the C. angustifolia marsh, compared to a reduction of 18.7–23.5% in the C. lasiocarpa marsh. The CO2-induced increase in CH4 emissions from the C. angustifolia marsh was paralleled with (1) increased dissolved organic carbon (DOC) released from plant photosynthesis and (2) reduced (rate of) CH4 oxidation due to a putative shift in methanotrophic community composition. In contrast, the CO2-induced decrease in CH4 emissions from the C. lasiocarpa marsh was associated with the increases in soil redox potential and pmoA gene abundance. We synthesized data from worldwide wetland ecosystems, and found that the responses of CH4 emissions to elevated CO2 was determined by the wetland water table levels and associated plant oxygen secretion capacity. In conditions with elevated CO2, plants with a high oxygen secretion capacity suppress CH4 emissions while plants with low oxygen secretion capacity stimulate CH4 emissions; both effects are mediated via a feedback loop involving shifts in activities of methanogens and methanotrophs.

Simultaneously Enhancing the Redox Potential and Stability of Multi-Redox Organic Catholytes by Incorporating Cyclopropenium Substituents.

High redox potential, two-electron organic catholytes for nonaqueous redox flow batteries were developed by appending diaminocyclopropenium (DAC) substituents to phenazine and phenothiazine cores. The parent heterocycles exhibit two partially reversible oxidations at moderate potentials [both at lower than 0.7 V vs ferrocene/ferrocenium (Fc/Fc+)]. The incorporation of DAC substituents has a dual effect on these systems. The DAC groups increase the redox potential of both couples by ∼300 mV while simultaneously rendering the second oxidation (which occurs at 1.20 V vs Fc/Fc+ in the phenothiazine derivative) reversible. The electron-withdrawing nature of the DAC unit is responsible for the increase in redox potential, while the DAC substituents stabilize oxidized forms of the molecules through resonance delocalization of charge and unpaired spin density. These new catholytes were deployed in two-electron redox flow batteries that exhibit voltages of up to 2.0 V and no detectable crossover over 250 cycles.

In situ electrochemical remediation of brackish river sediment rich in aromatic organic matter using steel-slag-combined sediment microbial fuel cells

Steel slag was employed as an additional substrate for power generation in sediment microbial fuel cells (SMFCs), and its role in the degradation of recalcitrant organic matter and sediment remediation was investigated. Steel slag improved the degradation of soil organic matter (SOM) in SMFC by 69 % compared to an individual SMFC with a 6.3-times higher charge production. Thermogravimetric and infrared spectroscopy analyses showed that steel slag humified SOM whereas the SMFC oxidatively degraded it. The humification by steel slag was attributed to the coordination with iron, it facilitated the accessibility of oxygen and stimulated oxidative degradation by the SMFC. As a result, aliphatic and aromatic compounds were degraded by 53 and 44 wt %, respectively, compared to the control. Additionally, ferrous ions eluted from the steel slag precipitated highly concentrated hydrogen sulfide as ferrous sulfide, leading to a noticeable increase in the voltage potential with respect to a standard hydrogen electrode (Eh) in the sediments. Overall, steel slag significantly enhances the efficiency of renewable energy production of SMFCs, and contributes to the remediation of benthic ecosystem by the development of aliphatic recalcitrant organic matter and increase in oxidation-reduction potential.

Weaning-associated feed deprivation stress causes microbiota disruptions in a novel mucin-containing in vitro model of the piglet colon (MPigut-IVM)

BackgroundRisk factors for the etiology of post-weaning diarrhea, a major problem in swine industry associated with enormous economic losses, remain to be fully elucidated. In concordance with the ethical concerns raised by animal experiments, we developed a new in vitro model of the weaning piglet colon (MPigut-IVM) including a mucin bead compartment to reproduce the mucus surface from the gut to which gut microbes can adhere.ResultsOur results indicated that the MPigut-IVM is able to establish a representative piglet archaeal and bacterial colon microbiota in terms of taxonomic composition and function. The MPigut-IVM was consequently used to investigate the potential effects of feed deprivation, a common consequence of weaning in piglets, on the microbiota. The lack of nutrients in the MPigut-IVM led to an increased abundance of Prevotellaceae and Escherichia-Shigella and a decrease in Bacteroidiaceae and confirms previous in vivo findings. On top of a strong increase in redox potential, the feed deprivation stress induced modifications of microbial metabolite production such as a decrease in acetate and an increase in proportional valerate, isovalerate and isobutyrate production.ConclusionsThe MPigut-IVM is able to simulate luminal and mucosal piglet microbiota and represent an innovative tool for comparative studies to investigate the impact of weaning stressors on piglet microbiota. Besides, weaning-associated feed deprivation in piglets provokes disruptions of MPigut-IVM microbiota composition and functionality and could be implicated in the onset of post-weaning dysbiosis in piglets.

Selenocompounds and Sepsis: Redox Bypass Hypothesis for Early Diagnosis and Treatment: Part A-Early Acute Phase of Sepsis: An Extraordinary Redox Situation (Leukocyte/Endothelium Interaction Leading to Endothelial Damage).

Significance: Sepsis is a health disaster. In sepsis, an initial, beneficial local immune response against infection evolves rapidly into a generalized, dysregulated response or a state of chaos, leading to multiple organ failure. Use of life-sustaining supportive therapies creates an unnatural condition, enabling the complex cascades of the sepsis response to develop in patients who would otherwise die. Multiple attempts to control sepsis at an early stage have been unsuccessful. Recent Advances: Major events in early sepsis include activation and binding of leukocytes and endothelial cells in the microcirculation, damage of the endothelial surface layer (ESL), and a decrease in the plasma concentration of the antioxidant enzyme, selenoprotein-P. These events induce an increase in intracellular redox potential and lymphocyte apoptosis, whereas apoptosis is delayed in monocytes and neutrophils. They also induce endothelial mitochondrial and cell damage. Critical Issues: Neutrophil production increases dramatically, and aggressive immature forms are released. Leukocyte cross talk with other leukocytes and with damaged endothelial cells amplifies the inflammatory response. The release of large quantities of reactive oxygen, halogen, and nitrogen species as a result of the leukocyte respiratory burst, endothelial mitochondrial damage, and ischemia/reperfusion processes, along with the marked decrease in selenoprotein-P concentrations, leads to peroxynitrite damage of the ESL, reducing flow and damaging the endothelial barrier. Future Directions: Endothelial barrier damage by activated leukocytes is a time-sensitive event in sepsis, occurring within hours and representing the first step toward organ failure and death. Reducing or stopping this event is necessary before irreversible damage occurs.