Eutrophication In Aquatic Systems Research Articles

A sustainable approach for efficient ammonium recovery, and simultaneous TOC removal from aqueous solutions by vesicle-like iron phosphate-based carbon nanomaterials

NH4+ is an ion with versatile potential; however, the release of wastewater containing this component, regardless of its high or low concentration, causes severe eutrophication in aquatic systems and contaminates numerous manufacturing processes. Thus, this study developed a sustainable method that can simultaneously remove, recover NH4+, polish water, oxidize organic matter, and yet release a material that can still be used as fertilizer. Regarding NH4+ removal, FeP400 rapidly exhibited an exceptional NH4+ uptake capacity (343.5 mg g-1) within 8 min, even in dairy processing wastewater with high NH4+ concentrations and diverse co-existing components. FeP400 could oxidize organic compounds spontaneously to remove TOC, indirectly enhancing its NH4+ uptake up to 33.5 % through charge balance mechanisms. The adsorption process involved both chemical (i.e., double-salt precipitation) and physical mechanisms (i.e., H-bonding and electrostatic interaction), as confirmed by thermodynamics, FT-IR, and XPS analyses. Regarding recovery, FeP400 can be reused for over 10 cycles with high removal (81 %) and NH4+ recovery (88 %), a significant improvement over conventional options. FeP400 also performed efficiently under flowing conditions using low-range NH4+ and TOC samples over 10 cycles, polishing not only 34.1 L of water with undetected NH4+, neutral pH, and extremely low TOC but also effectively recovering the NH4+ uptake at an economical cost. Lastly, its environmentally friendly nature, which contains essential nutrients for plant growth, further enhances its recyclability after release. Thus, FeP400 is believed to offer a transformative, sustainable, and highly efficacious solution to the NH4+contamination and critical ultrapure water issues that industries urgently address.

Using oxygen isotopes in phosphate to assess biological phosphorus cycling in a small and shallow freshwater lake system

AbstractReducing excess phosphorus (P) loads that cause eutrophication in aquatic systems is essential for meeting water quality standards. The oxygen isotopic composition of phosphate (δ18Op) is a powerful tool for tracking P sources and cycling in diverse natural ecosystems. Here, we use δ18Op distribution in a small freshwater body (a lagoon–lake system) with high biological activity. We report δ18Op values seasonally along the water flow path in lagoon–lake system adjacent to Lake Biwa, Japan. The δ18Op values of inflowing water originating as agricultural runoff were constant throughout the study period at +16.3‰ ± 0.2‰. The δ18Op values in the system were generally offset from temperature‐dependent isotopic equilibrium with the surrounding water, ranging from +11.1‰ to +17.8‰. The δ18Op values of the lake water approached equilibrium values in July and October, when dissolved inorganic P (DIP) retention rates were high, consistent with extensive biologically mediated phosphate cycling. A δ18Op two end‐member mixing model, involving inflowing P and biologically recycled P, suggests that P turnover rates in the lagoon–lake system were high during the productive seasons. In contrast, the longer lake water residence time in the non‐irrigation season (winter) allowed δ18Op values to deviate toward lower values relative to both equilibrium and agricultural source δ18Op values, suggesting that P metabolism was dominated by extracellular/ecto‐enzymatic hydrolysis of dissolved organic P under low DIP concentrations. This work highlighted the utility of δ18Op for understanding P dynamics in shallow lake ecosystems.

Phytoplankton Community Dynamics in Ponds with Diverse Biomanipulation Approaches

The rising challenge of eutrophication in aquatic systems globally necessitates an understanding of phytoplankton community dynamics under diverse biomanipulation approaches. This study, conducted from June 2022 to July 2023 in the Yuqiao Reservoir’s ponds in China, explored phytoplankton dynamics across ponds under different biomanipulation strategies. The study included a pond (BL) without fish stocking, a pond (CH) stocked with carnivorous and herbivorous fish, and another pond (CFD) incorporating a mix of carnivorous, filter-feeding, and detritus-feeding fish. Substantial seasonal variations in phytoplankton density and biomass were observed. In the BL pond, phytoplankton density ranged from 0.23 × 107 to 3.21 × 107 ind/L and biomass from 0.71 to 7.10 mg/L, with cyanobacteria predominantly in warmer seasons and a shift to cryptophytes and chrysophytes in winter. The CH pond exhibited a density range from 0.61 × 107 to 8.04 × 107 ind/L and biomass of 1.11 to 7.58 mg/L. Remarkably, the CFD pond demonstrated a significant reduction in both density (0.11 × 107 to 2.36 × 107 ind/L) and biomass (0.27 to 5.95 mg/L), indicating the effective implementation of its biomanipulation strategy. Key environmental factors including total nitrogen, water temperature, pH, chlorophyll-a, and total phosphorus played a significant role in shaping phytoplankton communities. The study highlights the importance of tailored biomanipulation strategies in aquatic ecosystem management, emphasizing long-term monitoring for sustainable management of eutrophication.

Urea–Lignin/Chitosan Nanocomposite as Slow-Release Nanofertilizer

Urea is a universal fertilizer, but its use efficiency hardly exceeds 30–35%, and more than 70% is lost to the environment, causing eutrophication in aquatic systems. This research focuses on encapsulating urea molecules using a lignin-chitosan composite. The nanocomposite was developed as a suitable carrier for entrapping nitrogenous fertilizer. Coconut coir contains plenty of lignin, which was extracted using the organosolv process by using ethanol as a solvent. Organosolv lignin (OSL) yielded spherical lignin nanoparticles (LNPs) via the solvent displacement method. Finally, a nitrogen source was loaded into the chitosan/lignin nanocomposite fertilizer (lignorea), which consists of LNPs, chitosan, and a cross-linker. The nanocomposite was characterized using PSA, SEM, TEM, UV–vis, FTIR, and XRD. The morphology of the OSL and LNPs was examined under SEM (626 ± 40 nm) and TEM (26 ± 9 nm). The noncrystallinity of both lignin and crystallinity after entrapment in nanocomposite was validated by XRD. The specific functional group pertaining to the lignin backbone had aromatic vibrations at 1511 cm–1 (OSL) and 1507 cm–1 (LNPs), and the presence of an amide peak after loading N was observed in FTIR. The lignin samples have their corresponding spectral absorbance at 281 and 288 nm wavelengths obtained in UV–vis. The size and stability of the extracted OSL and LNPs were verified by a particle size analyzer and zeta potential, respectively. The compatibility and interactions of the developed nanofertilizer were confirmed with molecular modeling and simulation. The developed nanofertilizer has total nitrogen of 30–35% which slowly releases up to 15 days in the soil. The study clearly suggests that lignin with chitosan served as a perfect template to hold and release N in a regulated pattern that collectively contributes to improved N use efficiency.

Modeling Topsoil Phosphorus—From Observation-Based Statistical Approach to Land-Use and Soil-Based High-Resolution Mapping

Phosphorus (P) is a macronutrient that often limits the productivity and growth of terrestrial ecosystems, but it is also one of the main causes of eutrophication in aquatic systems at both local and global levels. P content in soils can vary largely, but usually, only a small fraction is plant-available or in an organic form for biological utilization because it is bound in incompletely weathered mineral particles or adsorbed on mineral surfaces. Furthermore, in agricultural ecosystems, plant-available P content in topsoil is mainly controlled by fertilization and land management. To understand, model, and predict P dynamics at the landscape level, the availability of detailed observation-based P data is extremely valuable. We used more than 388,000 topsoil plant-available P samples from the period 2005 to 2021 to study spatial and temporal variability and land-use effect on soil P. We developed a mapping approach based on existing databases of soil, land-use, and fragmentary soil P measurements by land-use classes to provide spatially explicit high-resolution estimates of topsoil P at the national level. The modeled spatially detailed (1:10,000 scale) GIS dataset of topsoil P is useful for precision farming to optimize nutrient application and to increase productivity; it can also be used as input for biogeochemical models and to assess P load in inland waters and sea.

Effect of Iron Availability on the Growth and Microcystin Content of Natural Populations of Microcystis spp. from Reservoirs in Central Argentina: A Microcosm Experiment Approach

The eutrophication of aquatic systems is a problem related to the contribution of excess nutrients—phosphorus (P) and nitrogen (N)—to water bodies, which produces an increase in cyanobacterial blooms. Under eutrophic conditions, P and N concentrations are sufficient for cyanobacteria growth, and some micronutrients are considered to become limiting for population growth. This work aimed to assess the effect of iron on cyanobacteria growth and the content of MCs in natural populations of Microcystis spp. Microcosm setting experiments were carried out with natural samples collected during two bloom events of Microcystis spp., kept under controlled light, temperature and pH conditions. The first bloom sample was exposed to different iron concentrations (400, 700 and 1100 µg Fe·L−1) to determine the optimum concentration for growth. The second was exposed to different iron addition modes (one: T1P, and two pulses: T2P) to imitate the iron increase produced by the downward migration of Microcystis spp. colonies. Our results show that iron is a growth-promoting factor and that its optimal range of concentrations for the growth of Microcystis spp. under the experimental setting conditions is between 700 and 1100 µg Fe·L−1. On the other hand, growth rates were not significantly different between T1P and T2P; thus, different addition modes did not have an effect on growth. Regarding microcystin content, the MC quota in natural populations of Microcystis spp. did not show a clear relationship with the iron supply. This work contributes to the understanding of the underlying factors affecting cyanobacteria bloom formation and the production of MCs, which in turn would impact the development of management strategies to control cyanobacteria blooms.

Effects of filtration timing and pore size on measured nutrient concentrations in environmental water samples

AbstractNutrient monitoring is important for informing management decisions to mitigate eutrophication in aquatic systems. Many nutrient monitoring programs use filter pore sizes that allow microorganisms to pass into samples and/or wait extended times between sample collection and filtration/preservation, allowing microbial processes to alter nutrient concentrations. Here, 34 sites were sampled to determine how filter pore size and filtration timing affected measured ammonium (NH4+) and orthophosphate (ortho‐P) concentrations. Three filter pore sizes (0.22, 0.45, and 0.70 μm) were used to filter water immediately upon collection and after 5 and 22 h in a bottle. NH4+ and ortho‐P concentrations varied relative to “baseline” measurements (i.e., 0.22 μm, field‐filtered samples), both over time and with different filter pore sizes, and showed no predictable direction of change based on ambient nutrient concentration or trophic status. As expected, larger relative changes occurred with lower ambient concentrations; however, for the entire dataset, samples with > 1 μmol L−1 ortho‐P and > 3 μmol L−1 NH4+ were lower by 11 and 33%, respectively, which would result in reported nutrient concentrations that were not representative of in situ conditions. Whole‐water samples filtered after 22 h varied up to 3070% for NH4+ and 480% for ortho‐P from baseline concentrations. Filtering water samples with a 0.22 filter (or 0.45 μm, at worst), immediately upon collection, should be adopted as standard practice to ensure that reported nutrient concentrations represent the most accurate measurement possible. Inconsistent and/or insufficient sampling and sample handling procedures can lead to poorly calibrated models and misinformed management and legislative decisions.

Nitrogen and Phosphorous Retention in Tropical Eutrophic Reservoirs with Water Level Fluctuations: A Case Study Using Mass Balances on a Long-Term Series

Nitrogen and phosphorous loading drives eutrophication of aquatic systems. Lakes and reservoirs are often effective N and P sinks, but the variability of their biogeochemical dynamics is still poorly documented, particularly in tropical systems. To contribute to the extending of information on tropical reservoirs and to increase the insight on the factors affecting N and P cycling in aquatic ecosystems, we here report on a long-term N and P mass balance (2003–2018) in Valle de Bravo, Mexico, which showed that this tropical eutrophic reservoir lake acts as a net sink of N (−41.7 g N m−2 y−1) and P (−2.7 g P m−2 y−1), mainly occurring through net sedimentation, equivalent to 181% and 68% of their respective loading (23.0 g N m−2 y−1 and 4.2 g P m−2 y−1). The N mass balance also showed that the Valle de Bravo reservoir has a high net N atmospheric influx (31.6 g N m−2 y−1), which was 1.3 times the external load and likely dominated by N2 fixation. P flux was driven mainly by external load, while in the case of N, net fixation also contributed. During a period of high water level fluctuations, the net N atmospheric flux decreased by 50% compared to high level years. Our results outlining water regulation can be used as a useful management tool of water bodies, by decreasing anoxic conditions and net atmospheric fluxes, either through decreasing nitrogen fixation and/or promoting denitrification and other microbial processes that alleviate the N load. These findings also sustain the usefulness of long-term mass balances to assess biogeochemical dynamics and its variability.

Production of agrocommodities and consumption of agrochemicals in Uruguay: its repercussions for aquatic systems / Produção de agrocommodities e consumo de agroquímicos no Uruguai: suas repercussões para os sistemas aquáticos

The objective of this study is to relate the amount of phosphorus (P) provided by agrochemicals (herbicides and phosphate fertilizers) to soil sown with genetically modified (GM) crops (soybeans and maize) with total phosphorus (TP) in waters of agricultural basins in Uruguay, South America. With this aim, the number of soybean and maize events resistant to glyphosate and glufosinate-ammonium, the total area sown with these GM crops, herbicides and phosphate fertilizers consumption, and TP in the main river of the country in the 2010-2019 period were considered. We found out that the relationship of the annual average of TP with P via herbicides is robust and statically significant, and the relationship with P contribution via fertilizers is strong but no statically significant. Therefore, herbicides must be taken into account as a probable cause of eutrophication of aquatic systems in order to achieve environmental standards.

Highly Efficient Removal of Nitrate and Phosphate to Control Eutrophication by the Dielectrophoresis-Assisted Adsorption Method.

The removal of excessive amounts of nitrate and phosphate from water sources, especially agricultural wastewater, has been of high significance to control eutrophication in aquatic systems. Here, a new method is reported for the removal of nitrate and phosphate simultaneously from wastewater based on the combination of the solution-phased adsorption (ADS) and dielectrophoresis (DEP) techniques. The plant ash was first selected as the adsorbent by screening tests, followed by a systematic investigation of using the adsorbent to remove nitrate and phosphate from wastewater under various experimental conditions, including the testing of adsorbent dosage, pretreatment time, water flow rate, and electrode voltage. The analysis of the adsorbent particles was also performed by scanning electron microscope (SEM) analysis, the energy dispersive X-ray spectroscopy (EDX) test, and the measurement of Zeta potentials. Compared with the ADS method alone, the introduction of DEP into the purification process has greatly increased the removal rate by 66.06% for nitrate and 43.04% for phosphate, respectively. In the meantime, it is observed that the processing time has been greatly reduced by 92% with the assistance of DEP.

Bioavailability of Various Phosphorus Fractions and Their Seasonality in a Eutrophic Estuary in the Southern Baltic Sea – A Laboratory Approach

Phosphorus (P) is a major driver of eutrophication, especially in anthropogenically impacted coastal waters, and determining its bioavailability is important for providing a good estimation of the eutrophication potential in aquatic systems. Therefore, we observed the bioavailability of P in four laboratory experiments on water samples collected in March, June, September, and December 2018. In the experiments, all P fractions of the sampled water were investigated in three treatments (“unfiltered” and “10 μm”- and “1.2 μm”-filtered). The bioavailability (utilization by organisms within several days) ranged from 9 to 100% for dissolved P, and 34 to 100% for particulate P. However, one of the particulate P fractions was bound in biomass and therefore was not directly bioavailable. The conditions in the March experiment represented a natural spring bloom with a residual potential for planktonic growth. In June and September, the nutrients needed for growth were depleted in the different treatments. In December, a spring bloom was simulated by the laboratory conditions. Preferential P uptake by a specific group of organisms could not be observed directly, although a trend of higher utilization of dissolved P by heterotrophic bacteria was observed. In conclusion, the bioavailable P (sum of dissolved P fractions and one particulate P fraction) accounted for between 20 and 94% of the total P. Consequently, our experiments demonstrated that the commonly monitored P fractions lead to an underestimation of the bioavailable P and thus of potential for eutrophication in aquatic systems, too.

Experimental Study of the Adsorption of Nitrogen and Phosphorus by Natural Clay Minerals

Nitrogen and phosphorus are commonly recognized as causing eutrophication in aquatic systems, and their transport in subsurface environments has also aroused great public attention. This research presented four natural clay minerals (NCMs) evaluated for their effectiveness of NH4 + and PO4 3- adsorption from wastewater. All the NCMs were fully characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), BET analysis, and adsorption kinetics and isotherms to better understand the adsorption mechanism-property relationship. The results show that the adsorption efficiency of the four NCMs for phosphate was better than that for ammonia nitrogen. The removal rate of phosphate was higher than 65%, generally in the range of 80%-90%, while the removal rate of ammonia nitrogen was less than 50%. The adsorption kinetic behavior followed the pseudo-second-order kinetic model. The ammonia nitrogen adsorption isotherm was in good agreement with the Freundlich isotherm equilibrium model, and the phosphate adsorption isotherm matched the Langmuir model. Among all the NCMs studied, bentonite (7.13 mg/g) and kaolinite (5.37 mg/g) showed higher adsorption capacities for ammonia nitrogen, while zeolite (0.21 mg/g) and attapulgite (0.17 mg/g) showed higher adsorption capacities for phosphate. This study provides crucial baseline knowledge for the adsorption of nitrogen and phosphate by different kinds of NCMs.

Co-composting invasive aquatic macrophytes and pond sediment holds the potential for environmental amelioration: Selecting the right shade of grey

Co-composting of invasive aquatic weeds with pond sediment can be a cost-effective way to manage the problem of invasion and eutrophication in aquatic systems and improvement of soil fertility in agricultural systems. Nevertheless, preparation of good quality compost is a challenge because of the variations in the physico-chemical properties of the plant material and the bulking agent. Mixing the plant biomass and the bulking agent in an appropriate proportion is crucial to make good quality compost, which requires a systematic empirical study. We standardized a protocol for composting Eichhornia crassipes and Ipomoea carnea biomass using pond sediment as a bulking agent. For each species, we used a randomized block design with 3 treatments × 3 replicates. The study revealed that mixing pond sediment and the weed biomass in 1:5 ratio yielded better quality compost in both the species compared to other treatments. The study emphasizes that composting aquatic weeds with pond sediment should help in managing the problem of weed invasion, sedimentation, eutrophication, and loss of soil fertility in agricultural fields.

Copper and Gold Nanoparticles Increase Nutrient Excretion Rates of Primary Consumers.

Freshwater ecosystems are exposed to engineered nanoparticles through municipal and industrial wastewater-effluent discharges and agricultural nonpoint source runoff. Because previous work has shown that engineered nanoparticles from these sources can accumulate in freshwater algal assemblages, we hypothesized that nanoparticles may affect the biology of primary consumers by altering the processing of two critical nutrients associated with growth and survivorship, nitrogen and phosphorus. We tested this hypothesis by measuring the excretion rates of nitrogen and phosphorus of Physella acuta, a ubiquitous pulmonate snail that grazes heavily on periphyton, exposed to either copper or gold engineered nanoparticles for 6 months in an outdoor wetland mesocosm experiment. Chronic nanoparticle exposure doubled nutrient excretion when compared to the control. Gold nanoparticles increased nitrogen and phosphorus excretion rates more than copper nanoparticles, but overall, both nanoparticles led to higher consumer excretion, despite contrasting particle stability and physiochemical properties. Snails in mesocosms enriched with nitrogen and phosphorus had overall higher excretion rates than ones in ambient (no nutrients added) mesocosms. Stimulation patterns were different between nitrogen and phosphorus excretion, which could have implications for the resulting nutrient ratio in the water column. These results suggest that low concentrations of engineered nanoparticles could alter the metabolism of consumers and increase consumer-mediated nutrient recycling rates, potentially intensifying eutrophication in aquatic systems, for example, the increased persistence of algal blooms as observed in our mesocosm experiment.

Molecular-level investigations of effective biogenic phosphorus adsorption by a lanthanum/aluminum-hydroxide composite

Biogenic phosphorus (P), such as organic P and inorganic pyrophosphates, could substantially contribute towards eutrophication in aquatic systems by internal loading of P from sediment through P species transformation. Previous eutrophication management studies mainly focus on the removal of orthophosphate (Ortho-P), however, an effective approach for biogenic P control from water sources, prior to incorporation in sediment, is still lacking. In this study, a lanthanum/aluminum-hydroxide (LAH) composite was demonstrated to provide both superior removal of Ortho-P and biogenic P, employing myo-inositol hexakisphosphate (IHP) and pyrophosphate (Pyro-P) as model compounds. The maximum IHP and Pyro-P adsorption capacities by LAH attained 36.4 and 21.8 mg P g−1, respectively. In order to understand the mechanisms of adsorption, zeta potential, 31P solid-state nuclear magnetic resonance (NMR) spectroscopy and P K-edge X-ray absorption near edge structure (XANES) techniques were used to characterize the LAH after adsorption. The results supported the hypothesis that the interaction between LAH and P species was through surface adsorption, by the formation of inner-sphere complexes. Linear combination fitting results of XANES data indicated that IHP and Pyro-P preferentially bonded with La-hydroxide in LAH. This study elucidates the adsorption properties and binding mechanisms of IHP and Pyro-P on lanthanum-bearing compounds at the molecular level, indicating that LAH is a promising material for the control of eutrophication.

Determination of Chemical Oxygen Demand in Water Samples Using Gas-phase Molecular Absorption Spectrometry.

Chemical oxygen demand (COD) is important for water quality assessment as it represents the level of reductive organic pollution from eutrophication in aquatic systems. For surface water quality monitoring, permanganate is usually applied as an oxidizing reagent, and the routine CODMn determination is mostly achieved by titration method. However, this titration method is tedious and time consuming, and the results suffer from environmental temperature fluctuations and complicated operation techniques. In this study, a novel CODMn determination method was developed using gas-phase molecular absorption spectrometry equipped with an online automated digestion device for the first time. The effects of digestion temperature, digestion time and sulfuric acid content were thoroughly studied. This method exhibited good linearity (0.35 to 12 mg/L), a low detection limit (0.12 mg/L), and good RSD from various water samples (0.71 - 2.37%). When used for CODMn determination in routine water quality monitoring, this automated GPMAS can considerably improve analysis speed, efficiency, accuracy and stability compared to the traditional titration method.

Spatial and seasonal phosphorus dynamics in a eutrophic estuary of the southern Baltic Sea

Phosphorus (P) is one of the major drivers of eutrophication in aquatic systems. Thus, knowledge of riverine P inputs into the Baltic Sea is essential to evaluate the eutrophication level. In eutrophic estuaries such as the Warnow Estuary, the traditionally monitored parameters of total P (TP) and dissolved molybdate-reactive P (DRP) are not adequate for such an evaluation. Over two years (September 2016 to August 2018), an extended monitoring programme was applied in the Warnow Estuary, determining dissolved non-molybdate-reactive P (DNP), particulate molybdate-reactive P (PRP), and particulate non-molybdate-reactive P (PNP) in addition to TP and DRP. Within the estuary, the concentrations of the P fractions varied on both spatial and seasonal scales. While a gradient in the surface water's PNP was found towards the Baltic Sea, in the bottom water the DRP was distinctive. Particulate P fractions dominated the productive phases (>50% of TP), whereas during regenerative periods dissolved P forms were dominant (>50% of TP). Even though diffusive pore water flux estimates showed a release of dissolved P from the sediment, the calculated TP loads (44 t TP a−1 in 2017) revealed a P retention of 12% within the Warnow Estuary. Although the reduction targets of the Baltic Sea Action Plan are presumably able to reach, further reductions are necessary to achieve the aims (good status according to eutrophication) of the Marine Strategy Framework Directive and the Water Framework Directive in the highly anthropogenically impacted Warnow Estuary.

Synthesis of a novel Fe-Mn binary oxide-modified lava adsorbent and its effect on ammonium removal from aqueous solutions.

Ammonium is strongly related to eutrophication and a key control of eutrophication in aquatic systems, especially in agricultural runoff. In this study, a novel Fe-Mn binary oxide-modified lava (FMML) granular adsorbent was synthesized for ammonium removal from aqueous solutions by co-precipitation method. The kinetic data were described by pseudo-second-order kinetic model well and intraparticle diffusion had effects on ammonium adsorption. For pH between 4.0 and 10.0, the adsorption efficiency was >80%, and its optimum was recorded at pH 7.0. FMML exhibited strong ammonium adsorption selectivity under the single presence of cations like Na+ , K+ , Ca2+ , and Mg2+ . The optimum adsorbent dose and particle size were 4g/L and 3-5mm, respectively, for an aqueous solution containing 10mg/L of ammonium under normal conditions (298K and pH 7.0). Furthermore, the adsorption process was endothermic, following both the Langmuir (R2 >0.98) and Freundlich (R2 >0.96) models. Compared with other adsorbents, the FMML can be prepared following a simpler protocol. After 30 times of adsorption-regeneration cycle, the FMML also had a relatively high ammonium adsorption capacity; hence, we see it as a prospective adsorbent for ammonium adsorption from aqueous solutions. PRACTITIONER POINTS: Fe-Mn binary oxide-modified lava with Fe/Mn ratio 3:1 was prepared using co-precipitation method. Adsorption maximum of modified lava was 20.8mg/g (298K and pH 7.0). Adsorption was sensitive to changes in adsorbent dose, particle size, and pH. Inorganic cations decreased ammonium adsorption in order of Na+ >K+ >Ca2+ >Mg2+ . Mechanisms for ammonium removal by FMML include diffusion, electrostatic attraction, oxidation, and complexation reaction.

Feedbacks between nitrogen fixation and soil organic matter increase ecosystem functions in diversified agroecosystems.

Nitrogen (N) losses from intensified agriculture are a major cause of global change, due to nitrate (NO3- ) export and the eutrophication of aquatic systems as well as emissions of nitrous oxide (N2 O) into the atmosphere. Diversified agroecosystems with legume cover crops couple N and carbon (C) inputs to soil and reduce N pollution, but there is a need to identify controls on legume N2 fixation across ecosystems with variable soil conditions. Here, I tested the hypothesis that N mineralization from turnover of soil organic matter (SOM) regulates legume N2 fixation across 10 farms that spanned a gradient of SOM levels. I separated soil samples into two SOM fractions, based on size and density, which are indicators of soil nutrient cycling and N availability (free particulate organic matter and intra-aggregate particulate organic matter [POM]). This study indicates downregulation of legume N2 fixation in diversified agroecosystems with increasing N availability in intra-aggregate POM and increasing N mineralization. Intercropping the legume with a grass weakened the relationship between N in POM and N2 fixation due to N assimilation by the grass. Further, mean rates of N and C mineralization across sites increased with two seasons of a legume-grass cover crop mixture, which could enhance this stabilizing feedback between soil N availability and N2 fixation over time. These results suggest a potential mechanism for the diversity-ecosystem-function relationships measured in long-term studies of agroecosystems, in which regular use of legume cover crops increases total soil organic C and N and reduces negative environmental impacts of crop production.

Using models of farmer behavior to inform eutrophication policy in the Great Lakes

To address the management of eutrophication in aquatic systems, the behavioral mechanisms that drive change at the individual level must be considered when designing policy interventions. This analysis identifies the beliefs that are critical to behavioral change, and explores the likelihood that farmers will adopt two management practices believed to be critical to reducing nutrient loading to recommended levels in Lake Erie. We find that there is potential for farmers to adopt key infield practices needed to reduce nutrient inputs. And further, that increased adoption of such practices is possible by increasing the perceived efficacy of the majority of farmers who are motivated to take action. Integrating these findings with physical models of nutrient movement indicates that adoption of these practices in combination with edge of field practices can attain phosphorus reduction targets for the lake. Future research should focus on measuring the effectiveness of education and outreach programs aimed at engaging farmers and promoting adoption of recommended practices. Such programs may only be effective if they are successfully building farmer confidence in their ability to implement the practices (i.e., perceived self efficacy) and increasing farmer's belief in the effectiveness of the practices at reducing nutrient loss and improving local water quality (i.e., perceived response efficacy).