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Impact of carbon dioxide level, water velocity, and feeding regimen on growth and fillet attributes of cultured rainbow trout (Oncorhynchus mykiss)

Production and management variables such as carbon dioxide (CO 2 ) level, water velocity, and feeding frequency influence the growth and fillet attributes of rainbow trout ( Oncorhynchus mykiss ), as well as cost of production. More information is needed to determine the contributions of these variables to growth and fillet attributes to find the right balance between input costs and fish performance. Two studies, of 84 and 90 days duration, were conducted to determine the effects of CO 2 level, water velocity, and feed frequency on rainbow trout growth, fillet yield, and fillet quality. In the first study, two CO 2 levels (30 and 49 mg/L) and two velocity levels (0.5 and 2.0 body lengths/s) were tested. In the second study two CO 2 levels (30 and 49 mg/L) and two feeding regimens (fed once daily to satiation or three times daily to satiation) were tested. In the first study, after 84 days, fillet weight from high CO 2 tanks was 13.5% lower than the fillet weights of fish from low CO 2 tanks. Percent fat of fillets was higher in low CO 2 fish ( P = 0.05) after 84 days and, fish from the low CO 2 treatment were larger ( P < 0.01). Both studies had similar results in regards to fat content and weight of fillets in response to elevated CO 2 levels. Velocity had little affect on either whole wet weight or fillet attributes of rainbow trout in this study. Muscle tissue contained more ( P < 0.01) fat when fish were fed three times daily (7.3%; day 90) compared to once daily (5.4%; day 90). Also, fish were larger (P < 0.05) when fed 3 times per day (1079 g; day 90) in comparison to only one daily feeding (792 g; day 90). Fish in high feed/high CO 2 tanks were larger and had more fillet fat than fish from low feed/low CO 2 tanks. To maximize rainbow trout growth at aquaculture facilities, management strategies should attempt to keep CO 2 levels below 30 mg/L when cost efficient. However, feeding 2–3 times daily should reduce production losses if CO 2 cannot be minimized. The effect of strain and velocity were minimal over the range we tested in comparison to the effects of CO 2 and feeding regimen.

Book chapter↗

Use of avoidance response by rainbow trout to carbon dioxide for fish self-transfer between tanks

Convenient, economical, and reduced labor fish harvest and transfer systems are required to realize operating cost savings that can be achieved with the use of much larger and deeper circular culture tanks. To achieve these goals, we developed a new technology for transferring fish based on their avoidance behavior to elevated concentrations of dissolved carbon dioxide (CO2). We observed this behavioral response during controlled, replicated experiments that showed dissolved CO2 concentrations of 60-120 mg/L induced rainbow trout (Oncorhynchus mykiss) to swim out of their 11 m3 "growout" tank, through a transfer pipe carrying a flow with ???23 mg/L dissolved CO2, into a second 11 m3 "harvest" tank. The research was conducted using separate groups of rainbow trout held at commercially relevant densities (40-60 kg/m3). The average weight of fish ranged from 0.15 to 1.3 kg during the various trials. In all trials that used a constant flow of low CO2 water (???23 mg/L) entering the growout tank from the harvest tank, approximately 80-90% of the fish swam from the growout tank, through the transfer pipe, and into the harvest tank after the CO2 concentration in the growout tank had exceeded 60 mg/L. The fish that remained in the growout tank stayed within the area of relatively low CO2 water at the entrance of the transfer pipe. However, the rate of fish transfer from the growout tank to the harvest tank was more than doubled when the diameter of the transfer pipe was increased from 203 to 406 mm. To consistently achieve fish transfer efficiencies of 99%, water flow rate through the fish transfer pipe had to be reduced to 10-20% of the original flow just before the conclusion of each trial. Reducing the flow of relatively low CO2 water near the end of each fish transfer event, restricted the zone of relatively low CO2 water about the entrance of the fish transfer pipe, and provided the stimulus for all but a few remaining fish to swim out of the growout tank. Results indicate that the CO2 avoidance technique can provide a convenient, efficient, more economical, and reduced labor approach for fish transfer, especially in applications using large and well mixed circular culture tanks. ?? 2007 Elsevier B.V. All rights reserved.

Aquacultural Engineering↗

Carbon dioxide stripping in aquaculture -- part III: model verification

Based on conventional mass transfer models developed for oxygen, the use of the non-linear ASCE method, 2-point method, and one parameter linear-regression method were evaluated for carbon dioxide stripping data. For values of K L a CO 2 < approximately 1.5/h, the 2-point or ASCE method are a good fit to experimental data, but the fit breaks down at higher values of K L a CO 2 . How to correct K L a CO 2 for gas phase enrichment remains to be determined. The one-parameter linear regression model was used to vary the C* CO 2 over the test, but it did not result in a better fit to the experimental data when compared to the ASCE or fixed C* CO 2 assumptions.

Aquacultural Engineering↗

Application of a fluidized bed reactor charged with aragonite for control of alkalinity, pH and carbon dioxide in marine recirculating aquaculture systems

Control of alkalinity, dissolved carbon dioxide (dCO 2 ), and pH are critical in marine recirculating aquaculture systems (RAS) in order to maintain health and maximize growth. A small-scale prototype aragonite sand filled fluidized bed reactor was tested under varying conditions of alkalinity and dCO 2 to develop and model the response of dCO 2 across the reactor. A large-scale reactor was then incorporated into an operating marine recirculating aquaculture system to observe the reactor as the system moved toward equilibrium. The relationship between alkalinity dCO 2 , and pH across the reactor are described by multiple regression equations. The change in dCO 2 across the small-scale reactor indicated a strong likelihood that an equilibrium alkalinity would be maintained by using a fluidized bed aragonite reactor. The large-scale reactor verified this observation and established equilibrium at an alkalinity of approximately 135 mg/L as CaCO 3 , dCO 2 of 9 mg/L, and a pH of 7.0 within 4 days that was stable during a 14 day test period. The fluidized bed aragonite reactor has the potential to simplify alkalinity and pH control, and aid in dCO 2 control in RAS design and operation. Aragonite sand, purchased in bulk, is less expensive than sodium bicarbonate and could reduce overall operating production costs.

Aquacultural Engineering↗

Vertical distribution of total carbon, nitrogen and phosphorus in riparian soils of Walnut Creek, southern Iowa

Subsurface lithology plays an important role in many riparian zone processes, but few studies have examined how sediment nutrient concentrations vary with depth. In this study, we evaluated concentrations of nutrients (N, C and P) with depth in a riparian zone of the glaciated Midwest. A total of 146 sediment samples were collected from 24 cores that extended to a maximum depth of 3.6??m at eight sites in the riparian zone of Walnut Creek. Subsurface deposits were predominantly silt loam, becoming coarser and more variable with depth. Nitrogen and carbon content ranged from < 0.01 to 0.42% and < 0.01 to 7.08%, respectively, and exhibited a strong trend of decreasing nutrient content with depth. In contrast, P concentrations averaged 574??mg/kg and did not vary systematically. Systematic variations in texture and nutrient content with depth largely corresponded to stratigraphic differentiation among the Camp Creek, Roberts Creek and Gunder members of the regionally recognized Holocene-age DeForest Formation. Variations in subsurface nutrient content were not found to be significantly related to present land cover, but land cover may have influenced nutrient content at the time of original sediment accumulation. Subsurface lithology and stratigraphy should be considered an important component in riparian zone studies where nutrient losses to streams via streambank erosion or groundwater discharge are assessed. ?? 2009 Elsevier B.V. All rights reserved.

Catena↗

Volatile fluxes through the Big Bend section of the San Andreas Fault, California: helium and carbon-dioxide systematics

To investigate the source of volatiles and their relationship to the San Andreas Fault System (SAFS), 18 groundwater samples were collected from wells near the Big Bend section of the SAFS in southern California and analyzed for helium and carbon abundance and isotopes. Concentrations of 4 He, corrected for air-bubble entrainment, vary from 4.15 to 62.7 (× 10 − 8 ) cm 3 STP g − 1 H 2 O. 3 He/ 4 He ratios vary from 0.09 to 3.52 R A (where R A = air 3 He/ 4 He), consistent with up to 44% mantle helium in samples. A subset of 10 samples was analyzed for the major volatile phase (CO 2 ) — the hypothesized carrier phase of the helium in the mantle–crust system: CO 2 / 3 He ratios vary from 0.614 to 142 (× 10 11 ), and δ 13 C (CO 2 ) values vary from − 21.5 to − 11.9‰ (vs. PDB). 3 He/ 4 He ratios and CO 2 concentrations are highest in the wells located in the Mil Potrero and Cuddy valleys adjacent to the SAFS. The elevated 3 He/ 4 He ratios are interpreted to be a consequence of a mantle volatile flux though the SAFS diluted by radiogenic He produced in the crust. Samples with the highest 3 He/ 4 He ratios also had the lowest CO 2 / 3 He ratios. The combined helium isotope, He–CO 2 elemental relationships, and δ 13 C (CO 2 ) values of the groundwater volatiles reveal a mixture of mantle and deep crustal (metamorphic) fluid origins. The flux of fluids into the seismogenic zone at high hydrostatic pressure may cause fault rupture, and transfer volatiles into the shallow crust. We calculate an upward fluid flow rate of 147 mm a − 1 along the SAFS, up to 37 times higher than previous estimates (Kennedy et al., 1997). However, using newly identified characteristics of the SAFS, we calculate a total flux of 3 He along the SAFS of 7.4 × 103 cm 3 STP a − 1 (0.33 mol 3 He a − 1 ), and a CO 2 flux of 1.5 × 10 13 cm 3 STP a − 1 (6.6 × 10 8 mol a − 1 ), ~ 1% of previous estimates. Lower fluxes along the Big Bend section of the SAFS suggest that the flux of mantle volatiles alone is insufficient to cause the super hydrostatic pressure in the seismogenic zone; however, results identify crustal (metamorphic) fluids as a major component of the CO 2 volatile budget, which may represent the additional flux necessary for fault weakening pressure in the SAFS.

California↗

Characterizing sedimentary organic carbon in a hydrothermal spreading center, the Escanaba Trough

Sediments in critical marine mineral environments are of wide importance due to their preservation of both marine minerals and organic carbon (OC) stocks. However, OC storage and cycling is often overlooked in mineral system studies. This work characterizes sedimentary OC within the Escanaba Trough, a hydrothermal sulfide system off the coast of northern California. By utilizing ROV-based push coring, we collected sediments near and far from high temperature, low temperature, and inactive vents. We applied a multipronged organic geochemical approach, measuring bulk sediment, OC fractions of varying labilities, and biomarkers to tease apart the storage, source, and cycling of OC within this complex system. In contrast to past work indicating a primarily terrestrial source to deeper, Pleistocene sediments, our results suggest a primarily marine source in surface sediments at least 50 m away from active venting. Near active venting, we see evidence of locally produced chemosynthetic OC in addition to the background marine source. This chemosynthetic OC appears to be rapidly remineralized and supports more complex deep-sea food webs compared to hemipelagic sites. Still, the greatest contribution of labile OC was observed at inactive vent sites, which we suggest is due to hydrothermal fluid alteration of more labile OC at actively venting sites. Depending on fluid temperature, hydrothermally altered OC is either preserved in the sediments as petroleum or migrated with fluid flow. Considering inactive sites are those most likely to be targeted by potential mining, we suggest additional studies could verify if these results apply at other sedimented seafloor massive sulfide systems.

California↗

Enhanced coal-dependent methanogenesis coupled with algal biofuels: Potential water recycle and carbon capture

Many coal beds contain microbial communities that can convert coal to natural gas (coalbed methane). Native microorganisms were obtained from Powder River Basin (PRB) coal seams with a diffusive microbial sampler placed downhole and used as an inoculum for enrichments with different nutrients to investigate microbially-enhanced coalbed methane production (MECoM). Coal-dependent methanogenesis more than doubled when yeast extract (YE) and several less complex components (proteins and amino acids) were added to the laboratory microcosms. Stimulated coal-dependent methanogenesis with peptone was 86% of that with YE while glutamate-stimulated activity was 65% of that with YE, and a vitamin mix had only 33% of the YE stimulated activity. For field application of MECoM, there is interest in identifying cost-effective alternatives to YE and other expensive nutrients. In laboratory studies, adding algal extract (AE) with lipids removed stimulated coal-dependent methanogenesis and the activity was 60% of that with YE at 27 d and almost 90% of YE activity at 1406 d. Analysis of British Thermal Unit (BTU) content of coal (a measure of potential energy yield) from long-term incubations indicated > 99.5% of BTU content remained after coalbed methane (CBM) stimulation with either AE or YE. Thus, the coal resource remains largely unchanged following stimulated microbial methane production. Algal CBM stimulation could lead to technologies that utilize coupled biological systems (photosynthesis and methane production) that sustainably enhance CBM production and generate algal biofuels while also sequestering carbon dioxide (CO 2 ).

International Journal of Coal Geology↗

Aluminum- and iron-based coagulation for in-situ removal of dissolved organic carbon, disinfection byproducts, mercury and other constituents from agricultural drain water

Agricultural production on wetland soils can be significant sources of dissolved organic carbon (DOC), disinfection byproduct precursors, mercury and nutrients to downstream water bodies and accelerate land subsidence. Presented as a potential solution for in-situ water quality improvement and land subsidence mitigation, chemically enhanced treatment wetlands (CETWs) were used to leverage both coagulation and wetland processes. In this study, we evaluated the performance of coagulants ferric sulfate (Fe dosing) and polyaluminum chloride (Al dosing) to remove pollutants from agricultural drain water using the coagulation system designed for CETWs. Both coagulation treatments removed over 70% DOC from source waters, resulting in removal efficiencies (mg-DOC removed per mg-metal dosed) of 1 under Al dosing and 0.5 under Fe dosing. Coagulation by both treatments preferentially removed UV254 active compounds compared to the bulk DOC concentration, suggesting coagulation targeted aromatics more effectively. Phosphates and haloacetic acids were also removed more readily, whereas trihalomethanes, dissolved organic nitrogen and filtered mercury species were removed at similar or lower rates than DOC. Dissolved inorganic nitrogen was not amenable to coagulation and removal was not observed. Freundlich, Langmuir and Monod models explained 33% of the variance for Al dosing and 78 – 89% of the variance for Fe dosing. All three models indicated Al dosing had higher removal efficiency and affinity for DOC than Fe dosing under study conditions, but when used to predict maximum removal efficiency there was no cohesiveness between the three models due to different model assumptions. Consideration of fluorescence dissolved organic matter and UV254 as surrogates for DOC concentration showed both were equally suitable before coagulant application, but as surrogates after coagulant application, neither could be deemed more fit as a surrogate since both were shown suitable for different treatment scenarios.

Ecological Engineering↗

The Importance of Uncertainty and Sensitivity Analysis in Process-based Models of Carbon and Nitrogen Cycling in Terrestrial Ecosystems with Particular Emphasis on Forest Ecosystems — Selected Papers from a Workshop Organized by the International Society for Ecological Modelling (ISEM) at the Third Biennal Meeting of the International Environmental Modelling and Software Society (IEMSS) in Burlington, Vermont, USA, August 9-13, 2006

Many process-based models of carbon (C) and nitrogen (N) cycles have been developed for terrestrial ecosystems, including forest ecosystems. They address many basic issues of ecosystems structure and functioning, such as the role of internal feedback in ecosystem dynamics. The critical factor in these phenomena is scale, as these processes operate at scales from the minute (e.g. particulate pollution impacts on trees and other organisms) to the global (e.g. climate change). Research efforts remain important to improve the capability of such models to better represent the dynamics of terrestrial ecosystems, including the C, nutrient, (e.g. N) and water cycles. Existing models are sufficiently well advanced to help decision makers develop sustainable management policies and planning of terrestrial ecosystems, as they make realistic predictions when used appropriately. However, decision makers must be aware of their limitations by having the opportunity to evaluate the uncertainty associated with process-based models ( Smith and Heath, 2001 and Allen et al., 2004 ). The variation in scale of issues currently being addressed by modelling efforts makes the evaluation of uncertainty a daunting task.

Ecological Modelling↗

Simulating the effects of management practices on cropland soil organic carbon changes in the Temperate Prairies Ecoregion of the United States from 1980 to 2012

Understanding the effects of management practices on soil organic carbon (SOC) is important for designing effective policies to mitigate greenhouse gas emissions in agriculture. In the Midwest United States, management practices in the croplands have been improved to increase crop production and reduce SOC loss since the 1980s. Many studies of SOC dynamics in croplands have been performed to understand the effects of management, but the results are still not conclusive. This study quantified SOC dynamics in the Midwest croplands from 1980 to 2012 with the General Ensemble Biogeochemical Modelling System (GEMS) and available management data. Our results showed that the total SOC in the croplands decreased from 1190 Tg C in 1980 to 1107 TgC in 1995, and then increased to 1176 TgC in 2012. Continuous cropping and intensive tillage may have driven SOC loss in the early period. The increase of crop production and adoption of conservation tillage increased the total SOC so that the decrease in the total SOC stock after 32 years was only 1%. The small change in average SOC did not reflect the large spatial variations of SOC change in the region. Major SOC losses occurred in the north and south of the region, where SOC baseline values were high and cropland production was low. The SOC gains took place in the central part of the region where SOC baseline values were moderate and cropland production was higher than the other areas. We simulated multiple land-use land-cover (LULC) change scenarios and analyzed the results. The analysis showed that among all the LULC changes, agricultural technology that increased cropland production had the greatest impact on SOC changes, followed by the tillage practices, changes in crop species, and the conversions of cropland to other land use. Information on management practice induced spatial variation in SOC can be useful for policy makers and farm managers to develop long-term management strategies for increasing SOC sequestration in different areas.

Ecological Modelling↗

Changes in organic carbon source and storage with sea level rise-induced transgression in a Chesapeake Bay marsh

Organic matter (OM) accumulation in marsh soils affects marsh survival under rapid sea-level rise (SLR). This work describes the changing organic geochemistry of a salt marsh located in the Blackwater National Wildlife Refuge on the eastern shore of Chesapeake Bay that has transgressed inland with SLR over the past 35–75 years. Marsh soils and vegetation were sampled along an elevation gradient from the intertidal zone to the adjacent forest, representing a space-for-time substitution of the process of marsh transgression. Stable carbon isotope analysis of bulk OM gives evidence for a transition from C3 upland-sourced OM to C4-dominated marsh vegetation over time. The vegetative source of the OM changes along a marsh-upland mixing line from herbaceous angiosperm-sourced lignin in the lower elevation marsh to a woody gymnosperm signature at the upper border of the marsh. The results of stable isotope and lignin analyses illustrate that landward encroachment of marsh grasses results in deposition of herbaceous tissues exhibiting relatively little decay. This presents a possible mechanism for OM stabilization as marshes migrate inland.

Maryland↗

Geochemical Modeling of Carbon Sequestration, MMV, and EOR in the Illinois Basin

The Illinois State Geologic Survey is conducting several ongoing CO 2 sequestration projects that require geochemical models to gain an understanding of the processes occurring in the subsurface. The ISGS has collected brine and freshwater samples associated with an enhanced oil recovery project in the Loudon oil field. Geochemical modeling allows us to understand reactions with carbonate and silicate minerals in the reservoir, and the effects they have had on brine composition. For the Illinois Basin Decatur project, geochemical models should allow predictions of the reactions that will take place before CO 2 injection begins. ?? 2009 Elsevier Ltd. All rights reserved.

Conference Paper↗

The U. S. Geological Survey carbon dioxide storage efficiency value methodology: Results and observations

In order to complete the 2013 U.S. Geological Survey (USGS) assessment of carbon dioxide (CO 2 ) storage resources , a methodology was needed to determine the CO 2 storage efficiency of individual rock strata . The method that was used involved a storage efficiency approximation by MacMinn et al. , combined with a brine viscosity model by Mao and Duan, and thermal and pressure data from petroleum fields across basins . The resulting efficiencies indicated that both salinity of the pore fluid and the thermal gradient have a strong effect on the amount of CO 2 that strata could store.

Energy Procedia↗

Significance of carbon dioxide density estimates for basin-scale storage resource assessments

The geologic carbon dioxide (CO 2 ) storage resource size is a function of the density of CO 2 in the subsurface. The pressure and temperature of the storage reservoir at depth affect the CO 2 density. Therefore, knowing these subsurface conditions allows for improved resource estimates of potential geologic CO 2 storage capacity. In 2012, the U.S. Geological Survey (USGS) completed an assessment of geologic CO 2 storage resources for large sedimentary basins in onshore and State waters areas of the U.S. Evaluating the subsurface conditions and CO 2 density in these basins was integral to the assessment. To better understand these conditions, investigations of pressure and temperature gradients, typically derived from borehole data and analog studies, were assembled at the basin scale. Based on the USGS assessment results and findings here, changes in subsurface pressure and temperature may yield density changes up to 40 percent, which may translate into significant changes in storage resource estimates.

Energy Procedia↗

Influence of natural dissolved organic carbon on the bioavailability of mercury to a freshwater alga

Bioavailability of mercury (Hg) to Selenastrum capricornutum was assessed in bioassays containing field-collected freshwater of varying dissolved organic carbon (DOC) concentrations. Bioconcentration factor (BCF) was measured using stable isotopes of methylmercury (MeHg) and inorganic Hg(II). BCFs for MeHg in low-DOC lake water were significantly larger than those in mixtures of lake water and high-DOC river water. The BCF for MeHg in rainwater (lowest DOC) was the largest of any treatment. Rainwater and lake water also had larger BCFs for Hg(II) than river water. Moreover, in freshwater collected from several US and Canadian field sites, BCFs for Hg(II) and MeHg were low when DOC concentrations were >5 mg L-1. These results suggest high concentrations of DOC inhibit bioavailability, while low concentrations may provide optimal conditions for algal uptake of Hg. However, variability of BCFs at low DOC indicates that DOC composition or other ligands may determine site-specific bioavailability of Hg.

Environmental Pollution↗

Mercury remediation in wetland sediment using zero-valent iron and granular activated carbon

Wetlands are hotspots for production of toxic methylmercury (MeHg) that can bioaccumulate in the food web. The objective of this study was to determine whether the application of zero-valent iron (ZVI) or granular activated carbon (GAC) to wetland sediment could reduce MeHg production and bioavailability to benthic organisms. Field mesocosms were installed in a wetland fringing Hodgdon Pond (Maine, USA), and ZVI and GAC were applied. Pore-water MeHg concentrations were lower in treated compared with untreated mesocosms; however, sediment MeHg, as well as total Hg (THg), concentrations were not significantly different between treated and untreated mesocosms, suggesting that smaller pore-water MeHg concentrations in treated sediment were likely due to adsorption to ZVI and GAC, rather than inhibition of MeHg production. In laboratory experiments with intact vegetated sediment clumps, amendments did not significantly change sediment THg and MeHg concentrations; however, the mean pore-water MeHg and MeHg:THg ratios were lower in the amended sediment than the control. In the laboratory microcosms, snails ( Lymnaea stagnalis ) accumulated less MeHg in sediment treated with ZVI or GAC. The study results suggest that both GAC and ZVI have potential for reducing MeHg bioaccumulation in wetland sediment.

Environmental Pollution↗

Thallium isotope evidence for a permanent increase in marine organic carbon export in the early Eocene

The first high resolution thallium (Tl) isotope records in two ferromanganese crusts (Fe-Mn crusts), CD29 and D11 from the Pacific Ocean are presented. The crusts record pronounced but systematic changes in 205Tl/203Tl that are unlikely to reflect diagenetic overprinting or changes in isotope fractionation between seawater and Fe-Mn crusts. It appears more likely that the Fe-Mn crusts track the Tl isotope composition of seawater over time. The present-day oceanic residence time of Tl is estimated to be about 20,000??yr, such that the isotopic composition should reflect ocean-wide events. New and published Os isotope data are used to construct age models for these crusts that are consistent with each other and significantly different from previous age models. Application of these age models reveals that the Tl isotope composition of seawater changed systematically between ~ 55??Ma and ~ 45??Ma. Using a simple box model it is shown that the present day Tl isotope composition of seawater depends almost exclusively on the ratio between the two principal output fluxes of marine Tl. These fluxes are the rate of removal of Tl from seawater via scavenging by authigenic Fe-Mn oxyhydroxide precipitation and the uptake rate of Tl during low temperature alteration of oceanic crust. It is highly unlikely that the latter has changed greatly. Therefore, assuming that the marine Tl budget has also not changed significantly during the Cenozoic, the low 205Tl/203Tl during the Paleocene is best explained by a more than four-fold higher sequestration of Tl by Fe-Mn oxyhydroxides compared with at the present day. The calculated Cenozoic Tl isotopic seawater curve displays a striking similarity to that of S, providing evidence that both systems may have responded to the same change in the marine environment. A plausible explanation is a marked and permanent increase in organic carbon export from ~ 55??Ma to ~ 45??Ma, which led to higher pyrite burial rates and a significantly reduced flux of Fe-Mn oxide removal as a result of increased biological uptake of Fe and Mn. ?? 2008 Elsevier B.V. All rights reserved.

Earth and Planetary Science Letters↗