Phosphate Concentration Research Articles

Environmental Impact of Choline Dihydrogenphosphate ([Chol][DHP]) on Seed Germination and Soil Microbial Activity

The applicability of ionic liquids has grown exponentially over the last few decades. This growth is due to the easy modification of these compounds formed by ions, through the proper choice of both moieties, and the possibility of introducing functional groups into their cations and anions. However, studies of their toxicity and effects on the environment remain scarce. This study analyses firstly the response to adding different concentrations of choline dihydrogen phosphate to the germination of seeds of eight plant species. It also examines the microbial population and the respiration of two soils with contrasting organic matter contents. Seeds were incubated in a Petri dish in a Phytotron with a photoperiod of 16 h under light at 24 °C and 8 h in darkness at 16 °C. The activity of microbial populations of untreated and treated soils was analysed by isothermal microcalorimetry at 25 °C. Basal soil respiration kinetics were measured at optimal moisture (80% of field water retention capacity) and temperature (25 °C) over 10 days. The results indicate that this compound has diverse effects on the different endpoints. Nevertheless, this compound can be classified as non-toxic considering its effects on seeds and on soil, at least in the medium- to long-term.

Distribution of nutrients and dissolved organic matter in a eutrophic equatorial estuary: the Johor River and the East Johor Strait

Abstract. Estuaries have strong physicochemical gradients that lead to complex variability and often high rates of biogeochemical processes, and they are also often impacted by humans. Yet, our understanding of estuarine biogeochemistry remains skewed towards temperate latitudes. We examined seasonal and spatial variability in dissolved organic matter (DOM) and nutrients along a partly eutrophic, agricultural–urban estuary system in Southeast Asia: the Johor River and the East Johor Strait. Dissolved organic carbon (DOC) and coloured DOM (CDOM) showed non-conservative mixing, indicating significant DOM inputs along the estuary. The CDOM spectral slopes and CDOM : DOC ratios suggest that terrigenous, soil-derived DOM dominates along the Johor River, while phytoplankton production and microbial recycling are important DOM sources in the Johor Strait. CDOM properties were not unambiguous source indicators in the eutrophic Johor Strait, which is likely due to heterotrophic CDOM production. Nitrate concentrations showed conservative mixing, while nitrite concentrations peaked at intermediate salinities of 10–25. Ammonium concentrations decreased with salinity in the Johor River but increased up to 50 µmol L−1 in the Johor Strait, often dominating the dissolved inorganic nitrogen (DIN) pool. Phosphate concentrations were low (<0.5 µmol L−1) throughout the Johor River but increased in the Johor Strait, where DIN : phosphate ratios were typically ≥ 16 : 1. This suggests that the Johor Strait may experience phosphorus limitation and that internal recycling is likely important for maintaining high nutrient concentrations in the Johor Strait. Overall, our results indicate that the Johor River and Johor Strait are clearly not part of the same estuarine mixing continuum and that nutrient recycling processes must be quantified to understand nutrient dynamics in the Johor Strait. Moreover, our results highlight the need for better techniques for DOM source tracing in eutrophic estuaries.

Preparation of a novel LC@MWCNTs membrane and its application for enhanced phosphate removal and fouling control

To control the eutrophication originating from phosphate discharge, a novel adsorptive membrane was prepared by vacuum filtrating lanthanum carbonate modified multi-walled carbon nanotubes (LC@MWCNTs) on the UF membrane. The LC@MWCNTs were firstly made using an in-situ method by adding MWCNTs to LaCl3·7H2O solution and forming lanthanum carbonate under alkaline conditions. The adsorption experiments exhibited that the maximum adsorption capacity of LC@MWCNTs was 77.58 mg P/g at pH 5. And the phosphate adsorption by LC@MWCNTs was not predominantly reliant on electrostatic interaction, but rather achieved through chemical interactions. Then, the prepared LC@MWCNTs membrane was systematically evaluated for its phosphate removal efficiency and anti-fouling performance during filtration. With the initial phosphate concentration of 1 mg P/L and membrane flux of 378 L·m−2 h−1, the phosphate removal by LC@MWCNTs membrane approached almost 100 %. Moreover, the LC@MWCNTs membrane exhibited higher permeability (281.6 L·m−2h−1bar−1) and effectiveness for humic acid (HA) removal (75 %), and LC@MWCNTs membrane mitigated the fouling caused by HA. XPS, FTIR and XRD elucidated that phosphate removal by LC@MWCNTs membrane primarily through the formation of La-O-P inner-sphere complexes via ligand exchange, resulting in the formation of adsorption product LaPO4·0.5H2O. Under strong alkaline conditions, the LC@MWCNTs membrane rapidly restored its phosphate removal performance (30 min) with no significant detachment of the LC@MWCNTs layer, indicating its good recovery and reusability performance. Additionally, the LC@MWCNTs membrane could continuously remove phosphate from actual water, confirming its potential for future practical applications.

Green solutions for antibiotic pollution: Assessing the phytoremediation potential of aquatic macrophytes in wastewater treatment plants

We compared the ability of one emergent (Sagittaria montevidensis), two floating (Salvinia minima and Lemna gibba), and one heterophyllous species (Myriophyllum aquaticum) to simultaneously remove sulfamethoxazole, sulfadiazine, ciprofloxacin, enrofloxacin, norfloxacin, levofloxacin, oxytetracycline, tetracycline, doxycycline, azithromycin, amoxicillin, and meropenem from wastewater in a mesocosm-scale constructed wetland over 28 days. Antibiotic concentrations in plants and effluent were analyzed using an LC-MS/MS to assess the removal rates and phytoremediation capacities. M. aquaticum did not effectively mitigate contamination due to poor tolerance and survival in effluent conditions. S. minima and L. gibba demonstrated superior efficiency, reducing the antibiotic concentrations to undetectable levels within 14 days, while S. montevidensis achieved this result by day 28. Floating macrophytes emerge as the preferable choice for remediation of antibiotics compared to emergent and heterophyllous species. Antibiotics were detected in plant tissues at concentrations ranging from 0.32 to 29.32 ng g−1 fresh weight, highlighting macrophytes' ability to uptake and accumulate these contaminants. Conversely, non-planted systems exhibited a maximum removal rate of 65%, underscoring the persistence of these molecules in natural environments, even after the entire experimental period. Additionally, macrophytes improved effluent quality regardless of species by reducing total soluble solids and phosphate concentrations and mitigating ecotoxicological effects. This study underscores the potential of using macrophytes in wastewater treatment plants to enhance overall efficiency and prevent environmental contamination by antibiotics, thereby mitigating the harmful impact on biota and antibiotic resistance. Selecting appropriate plant species is crucial for successful phytoremediation in constructed wetlands, and actual implementation is essential to validate their effectiveness and practical applicability.

Dimensions of muddy brown granular casts in patients with acute tubular injury

BackgroundThe presence of “muddy” brown granular casts (MBGC) in the urine sediment is pathognomonic for acute tubular injury (ATI). Although MBGC have been noted for years, there are no reports regarding their length nor width. The objective of this study was to measure MBGC using images obtained by light microscopy and investigate associations with clinically relevant parameters. MethodsPatients with diagnosis of ATI as evidenced by visualization of abundant MBGC (>30% low power fields) were sampled. Bright-field images were measured using ImageJ. Twenty-five patients were included: 44% women; median age 64 yrs; 52% white, 36% black. Mean MBGC width (n = 350) was 34.4 ± 13.1 µm (range: 9 to 110 µm). ResultsMean MBGC length was 98.7 ± 42.7 µm (range: 33 to 317 µm). Based on a previous report of cortical tubular diameters, MBGC width corresponded well with the median reported range. MBGC width was positively correlated with patient height (ρ=0.41, p=0.04), and length was positively correlated with fractional excretion of sodium (ρ=0.57. p=0.02) and urine chloride concentration (ρ=0.90, p=0.001). Mean MBGC length was negatively correlated with age (ρ=-0.47, p=0.02) and urine phosphate concentration (ρ=-0.72, p=0.03). There were no differences between cases that required renal replacement therapy (RRT, n =10) and those that did not require RRT (n=15). ConclusionThis is the first study reporting dimensions of MBGC from cases with ATI. Clinical implications of these observations require further study.

A clade of receptor-like cytoplasmic kinases and 14-3-3 proteins coordinate inositol hexaphosphate accumulation

Inositol hexaphosphate (InsP6) is the major storage form of phosphorus in seeds. Reducing seed InsP6 content is a breeding objective in agriculture, as InsP6 negatively impacts animal nutrition and the environment. Nevertheless, how InsP6 accumulation is regulated remains largely unknown. Here, we identify a clade of receptor-like cytoplasmic kinases (RLCKs), named Inositol Polyphosphate-related Cytoplasmic Kinases 1-6 (IPCK1-IPCK6), deeply involved in InsP6 accumulation. The InsP6 concentration is dramatically reduced in seeds of ipck quadruple (T-4m/C-4m) and quintuple (C-5m) mutants, accompanied with the obviously increase of phosphate (Pi) concentration. The plasma membrane-localized IPCKs recruit IPK1 involved in InsP6 synthesis, and facilitate its binding and activity via phosphorylation of GRF 14-3-3 proteins. IPCKs also recruit IPK2s and PI-PLCs required for InsP4/InsP5 and InsP3 biosynthesis respectively, to form a potential IPCK-GRF-PLC-IPK2-IPK1 complex. Our findings therefore uncover a regulatory mechanism of InsP6 accumulation governed by IPCKs, shedding light on the mechanisms of InsP biosynthesis in eukaryotes.

Phosphate-solubilizing rhizobacteria and their effects on the growth and phosphorus uptake by wheat plants

Wheat represents a fundamental component of the diet that contributes to ensuring global food security. However, its cultivation faces various abiotic and biotic constraints that result in fluctuating yields. The use of plant growth promoting rhizobacteria (PGPR) with the ability to solubilize phosphate presents itself as an environmentally friendly solution aimed to at enhancing sustainable agriculture practices. The objective of the present study is to assess the potential of PGPR in augmenting both yield and phosphorus (P) levels in wheat plants (Triticum durum L). under semi-controlled environmental conditions. Initially, the strains under investigation were screened for their capacity to dissolve different forms of mineral complex P, along with other plant growth promoting attributes such as iron chelation, Indole acetic acid (IAA) production, nitrogen fixation, and production of exopolysaccharides. Plant response to inoculation with PGPR was studied through an experiment conducted in a greenhouse involving four distinct treatments: (1) Control plants without any inoculation, (2) Inoculation with the PGP27 strain (Rahnella aquatilis), (3) Inoculation with the PGP25 strain (Erwinia persicina), and (4) Inoculation with the PGP374 strain (Raoultella terrigena). Results demonstrated that the studied strains exhibited significant promoting activities, including the solubilization of complex phosphate, the production of exopolysaccharides, IAA, siderophores, and atmospheric nitrogen fixation. Furthermore, the inoculation of plants with PGPR led to an increase in both biomass and plant phosphate concentrations, surpassing those observed in the control group. In conclusion, the findings propose that species like Raoultella and Erwinia have the potential to offer agronomic advantages as rhizobacteria that promote plant growth.

Isotherm, Kinetics, and Adsorption Mechanism Studies of Coal Gasification Coarse Slag as Highly Efficient Phosphate Adsorbents

This study investigates the efficacy of a novel low-cost phosphate adsorbent, denoted as SH-CGCS, derived from coal gasification coarse slag (CGCS) via an alkali activation method. SH-CGCS is a mesoporous material with a specific surface area (64 m2/g) approximately six times larger than CGCS (11 m2/g), which enhances its adsorption capacity compared with CGCS. Furthermore, SH-CGCS achieves a phosphate adsorption capacity of 38.5 mg/g in strongly acidic water (pH 3) and demonstrates robust acid resistance, which makes it particularly effective for phosphate removal from acidic wastewater. Results from coexisting anion experiments affirm the good adsorption selectivity of SH-CGCS for phosphate. Moreover, SH-CGCS exhibits proficiency in treating water containing low phosphate concentrations under flowing conditions. The maximum phosphate adsorption capacity of SH-CGCS calculated using the Langmuir model is 23.92 mg/g, surpassing that of other reported adsorbents. Importantly, saturated SH-CGCS can be regenerated and reused, which contributes to its practical applicability. The adsorption mechanisms of SH-CGCS for phosphate involve ligand exchange, inner-sphere complexation, surface precipitation, and electrostatic adsorption. Thus, this study not only enhances the overall utility of CGCS but also presents a simple and efficient method for removing phosphate. Our findings indicate that SH-CGCS holds considerable potential as a phosphate adsorbent, offering a promising solution for wastewater treatment.

Hybridized machine learning models for phosphate pollution modeling in water systems for multiple uses

Phosphate pollution in water bodies is a significant environmental concern, especially in regions with extensive agricultural practices. Hence, a tool for accurately assessing the phosphate concentration is essential. This research paper explores the effectiveness of machine learning (ML) models combined with nature-inspired optimization algorithms for predicting phosphate levels in water systems. The novelty consists of integrating the power of machine learning models, which have been presenting excellent performance at capturing complex relationships in environmental pollution data, with the Harris Hawks Optimizer (HHO) optimization capabilities inspired by hawks' hunting behavior. Four hybrid implementations combining the HHO were evaluated, and four feature subsets were assessed to identify the most influential variables in the modeling process. Using water quality data from Brazilian upstream watersheds, the hybrid models were trained and validated, enabling accurate and robust predictions of phosphate concentrations. The elastic net (EN) model optimized by Harris Hawk Optimizer (HHO-EN) produced the best-averaged performance among all experiments (R = 0.825, R2 = 0.670, Root Mean Square Error (RMSE) = 0.049 mg/L, Mean Absolute Error (MAE) = 0.037 mg/L). A parametric and feature importance analysis identified the most influential parameters in the contamination modeling process. Hybrid machine learning models represent a novel and efficient strategy for water quality monitoring and environmental management, supporting the preservation of aquatic ecosystems.

Unraveling marine phosphogenesis along the Miocene coast of Peru: Origin and sedimentological significance of the Pisco Formation phosphorites

Phosphorite deposits form through phosphogenesis, a mechanism of diffusion and concentration of interstitial phosphate in sediments leading to Ca-phosphate mineral precipitation in a favorable sedimentary regime at the seafloor. Stretching along the Peruvian coast, the East Pisco Basin is known to host phosphorite beds of Miocene age. In this study, we investigate the petrographic, mineralogical and chemical composition of the Miocene phosphorite layers of the East Pisco Basin, and discuss the phosphogenetic mechanism(s) and sedimentary dynamics that led to the genesis and accumulation of P-rich deposits. Phosphorite samples were collected from layers overlaying stratigraphic unconformities within the Pisco Formation and subsequently analyzed through multiple methods: optical microscopy, XRD, XRF, SEM-EDS, EPMA, ICP-MS and LA-ICP-MS. Our results indicate that these layers consist of phosphatic clasts and nodules along with dolomite clasts, basement boulders, shark teeth, mollusk molds and vertebrate bone fragments. The P-rich clasts are mainly composed of phosphatic intraclasts and small phosphatic nodules. They occur associated with minor amounts of dolomite clasts coated by Fe-oxyhydroxides and laminites. Clasts and nodules are cemented by both early and late diagenetic cements, such as dolomite, calcite, silica, gypsum/anhydrite and baryte. Our observations suggest that the Pisco phosphorite deposits are transgressive lags laying on ravinement surfaces. They formed just below the sediment-water boundary during the early transgression phases, when the porewaters were enriched in phosphorus due to the abundance of organic-rich sediments and the microbial activity, as typical of upwelling settings. These deposits formed in shallow marine conditions, characterized by high biological productivity and low net sedimentation rates, with suboxic conditions at and beneath the sediment-water interface. The concentration of phosphate-coated clasts was then favored by a sedimentary condensation mechanism of dynamic bypassing. Overall, this study provides new insights into the genesis of phosphorite layers in the East Pisco Basin and highlights the importance of understanding the complex interplay between authigenic and sedimentological processes in the formation of these economically and geologically relevant sedimentary rocks.

Simultaneous removal of ammonium, phosphate, and phenol via self-assembled biochar composites CBCZrOFe3O4 and its utilization as soil acidity amelioration

ABSTRACT High concentrations of ammonium, phosphate, and phenol are recognized as water pollutants that contribute to the degradation of soil acidity. In contrast, small quantities of these nutrients are essential for soil nutrient cycling and plant growth. Here, we reported composite materials comprising biochar, chitosan, ZrO, and Fe3O4, which were employed to mitigate ammonium, phosphate, and phenol contamination in water and to lessen soil acidity. Batch adsorption experiments were conducted to assess the efficacy of the adsorbents. Initially, comparative studies on the simultaneous removal of NH4, PO4, and phenol using CB (biochar), CBC (biochar + chitosan), CBCZrO (biochar + chitosan + ZrO), and CBCZrOFe3O4 (biochar + chitosan + ZrO + Fe3O4) were conducted. The results discovered that CBCZrOFe3O4 exhibited the highest removal percentage among the adsorbents (P < 0.05). Adsorption data for CBCZrOFe3O4 were well fitted to the second-order kinetic and Freundlich isotherm models, with maximum adsorption capacities of 112.65 mg/g for NH4, 94.68 mg/g for PO4 and 112.63 mg/g for phenol. Subsequently, the effect of CBCZrOFe3O4-loaded NH4, PO4, and phenol (CBCZrOFe3O4-APP) on soil acidity was studied over a 60-day incubation period. The findings showed no significant changes (P < 0.05) in soil exchangeable acidity, H+, Mg, K, and Na. However, there was a substantial increase in the soil pH, EC, available P, CEC, N-NH4, and N-NO3. A significant reduction was also observed in the available soil exchangeable Al and Fe (P < 0.05). This technique demonstrated multi-functionality in remediating water pollutants and enhancing soil acidity.

Phosphates on Mars and Their Importance as Igneous, Aqueous, and Astrobiological Indicators

This paper reviews the phosphate phases in meteorites and those measured by landed spacecraft, what they reveal about past igneous and aqueous conditions on Mars, and important implications for potential prebiotic chemistry, past habitability, and potential biosignatures that could be detected in samples returned from Mars. A review of the 378 martian meteorites as of 2023 indicate that of the two most common phosphate minerals in Mars meteorites, merrillite and apatites, the apatite composition is largely F- and Cl-rich, with shergottites containing more OH. The phosphate concentrations examined across multiple missions show a relatively narrow range of phosphate, with higher concentrations observed in the Mount Sharp Group in Gale crater and Wishstone at Gusev crater and lower concentrations observed at Jezero crater floor and Jezero fan. Possible secondary phosphates detected on Mars, including Fe phosphates at Jezero crater and Gusev crater and Ca- and Al-bearing secondary phosphates, temperatures of formation of secondary phases and their dissolution rates and solubilities are reviewed and summarized. Despite this wealth of information about phosphates on Mars, due to their fine scale and relatively low concentrations, Mars Sample Return is needed to better understand phosphate and its implications for the igneous, aqueous, and astrobiological history of Mars.

Spontaneous Tumor Regression and Reversion: Insights and Associations with Reduced Dietary Phosphate.

Tumors that spontaneously shrink from unknown causes in tumor regression, and that return to normal cells in tumor reversion, are phenomena with the potential to contribute new knowledge and novel therapies for cancer patient survival. Tumorigenesis is associated with dysregulated phosphate metabolism and an increased transport of phosphate into tumor cells, potentially mediated by phosphate overload from excessive dietary phosphate intake, a significant problem in Western societies. This paper proposes that reduced dietary phosphate overload and reregulated phosphate metabolism may reverse an imbalance of kinases and phosphatases in cell signaling and cellular proliferation, thereby activating autophagy in tumor regression and reversion. Dietary phosphate can also be reduced by sickness-associated anorexia, fasting-mimicking diets, and other diets low in phosphate, all of which have been associated with tumor regression. Tumor reversion has also been demonstrated by transplanting cancer cells into a healthy microenvironment, plausibly associated with normal cellular phosphate concentrations. Evidence also suggests that the sequestration and containment of excessive phosphate within encapsulated tumors is protective in cancer patients, preventing the release of potentially lethal amounts of phosphate into the general circulation. Reducing dietary phosphate overload has the potential to provide a novel, safe, and effective reversion therapy for cancer patients, and further research is warranted.

Assessment of phosphatemia at admission to the intensive care unit to predict mechanical ventilation among patients with acute exacerbation of chronic obstructive pulmonary disease: a retrospective cohort study.

Hypophosphatemia has been reported to impair diaphragmatic function in patients with chronic obstructive pulmonary disease (COPD). However, little is known about the role of dysphosphatemia at admission [plasmatic phosphate concentration at intensive care unit (ICU) admission (T0-Ph)] to the ICU and respiratory outcomes among patients with severe acute COPD exacerbation. We aimed to assess the value of T0-Ph as a predictive factor of invasive mechanical ventilation (MV) during ICU stay. We retrospectively included consecutive patients admitted to the ICU for a severe acute exacerbation of COPD between May 2015 and December 2018. Logistic multivariate regression analysis was performed to identify association between T0-Ph and the need for invasive MV during the ICU stay. We included 198 patients of whom 132 (67%) were male. The median age was 70 [interquartile range (IQR), 61-77] years. Nine (4.5%) patients died in the ICU. Median T0-Ph was significantly higher among patients requiring invasive MV as compared to non-intubated patients [1.23 (IQR, 1.07-1.41) and 1.09 (IQR, 0.91-1.27) mmol/L; P=0.005]. By multivariate analysis, pneumonia [odds ratio (OR) =6.42; 95% confidence interval (CI): 2.78-15.96; P<0.0001) and a history of intubation (OR =3.33; 95% CI: 0.97-11.19; P=0.05) were independently associated with the need for invasive MV, whereas T0-Ph was not (OR =1.75; 95% CI: 0.72-4.44; P=0.22). T0-Ph was significantly higher in patients requiring invasive MV. However, T0-Ph was not associated with the need for invasive MV in multivariate analysis.

Anthropogenically Driven Changes in the Carbon to Phosphorus Ratio of Marine Dissolved Organic Matter

AbstractMarine dissolved organic matter (DOM) cycles play a pivotal role in sustaining marine ecosystems and regulating the ocean's carbon sequestration from the atmosphere. However, the response of DOM cycles, including dissolved organic carbon (DOC) and dissolved organic phosphorus (DOP), to future climate change remains highly uncertain. Using the Community Earth System Model version 2 large ensemble simulations, we find that the C:P ratios in DOM are projected to increase by up to two‐fold in oligotrophic gyres by 2100. Increased upper ocean stratification reduces surface phosphate availability, thereby elevating phytoplankton C:P ratios and enhancing phytoplankton utilization of DOP, both acting to deprive DOM of P. Moreover, ocean stratification has a direct effect on exporting less DOC to the subsurface while accumulating more DOC at the sea surface. As a result of the strong sensitivity to ocean surface warming, the anthropogenically driven trends in upper ocean DOM concentration and its C:P ratios are estimated to emerge earlier from the simulated natural variability than upper ocean phosphate concentrations and net primary production—two key biogeochemical variables that are frequently monitored. This study suggests that changes in the C:P ratios of DOM could serve as a sensitive fingerprint of anthropogenic ocean warming, potentially exerting broad impacts on marine microbes. Our estimated 4% reduction in the globally integrated DOC export below 100 m is comparable to a 2% reduction in particulate organic carbon (POC) export by 2100, implying that global warming is likely to weaken the biological carbon pump through both DOC and POC.

Phosphaturia in HIV-Exposed Uninfected Neonates Associated with Maternal Use of Tenofovir Disoproxil Fumarate in Late Pregnancy.

Tenofovir disoproxil fumarate (TDF) is often used in treating pregnant women living with HIV. Third-trimester TDF exposure is associated with a 12% reduction in bone mineral content in HIV-exposed uninfected (HEU) neonates. The potential mechanisms underlying this observation are unknown. The TDF study enrolled newborns of gestational age ≥36 weeks from the Surveillance Monitoring for Antiretroviral Therapy and Toxicities study based on in utero TDF exposure (TDF use ≥8 weeks in the third trimester vs none). Blood and urine samples were collected cross-sectionally within 30 days of birth to assess renal function (serum creatinine, serum phosphate, eGFR, percent tubular reabsorption of phosphate [PTRP]), and bone turnover (serum parathyroid hormone, 25-OH vitamin D [25(OH)D], and urinary cross-linked N-telopeptide of type 1 collagen). For each biomarker, a LOESS plot was fit using values at age at specimen collection; regression lines over age were fit among samples collected from 4 to 30 days, to compare slopes by TDF exposure. Among 141 neonates, 77 were TDF-exposed and 64 TDF-unexposed. Between age 4 and 30 days, PTRP decreased more rapidly in the TDF-exposed compared to the unexposed group with slopes of -0.58 vs -0.08/day (difference -0.50/day [95% CI -0.88, -0.11]). Slopes for 25(OH)D were similar in both groups, but serum levels were lower in TDF-exposed neonates (median [IQR]: 22 [19, 29] vs 26 [22, 37] ng/mL). No differences were observed for other biomarkers. Third-trimester in utero exposure to TDF is associated with increased urinary loss of phosphate and lower serum concentrations of 25(OH)D in HEU neonates.

Effect of Phosphate Concentration on Anodizing Process Efficiency and Aluminium Surface Hardness in 16% Sulfuric Acid Solution

Effect of Phosphate Concentration on Anodizing Process Efficiency and Aluminium Surface Hardness in 16% Sulfuric Acid Solution

Boosting the visible-light-driven photocatalytic efficiency in porous Cu/TiO2 ceramic coatings

In this study, we examined how current density, sodium phosphate concentration, and the addition of copper sulfate to the supporting electrolyte affect PEO coatings on pure titanium. The chemical composition, morphology, and optical behavior of PEO coatings were extensively analyzed using scanning electron microscopy (SEM), X-ray diffraction (XRD), and UV–Vis diffuse reflectance spectroscopy (DRS). With an increase in current density from 6 to 18 A/dm2, the coating's pore size enlarges and the rutile phase content within the coatings increases. The coating created at 12 A/dm2 shows the highest photocatalytic activity and triggers a unique three-stage behavior in the voltage-time diagram. Adding 4 g/l of CuSO4 to the electrolyte resulted in the formation of an unwanted Cu-based precipitates, causing electrolyte instability. To stabilize it, potassium hydroxide was removed, and the base electrolyte concentration was adjusted. To address this issue, potassium hydroxide was eliminated from the supporting electrolyte. Subsequently, the concentration of the base electrolyte was optimized. Also, the synergistic influence of CuSO4 addition (4 g/l) to the supporting electrolyte at different concentrations of 5, 10, and, 15 g/l of trisodium phosphate on PA was investigated. The superior photocatalytic performance of the optimum coating created in the electrolyte containing 5 g/l trisodium phosphate and 4 g/l CuSO4 is attributed to its enhanced porous structure, along with the heterojunction between the anatase and rutile phases. These features significantly boost the available surface area and facilitate the efficient separation and transfer of photogenerated charge carriers. Ultimately, a mechanism for MB photodegradation was proposed based on the findings from Mott-Schottky analysis and DRS.

Cryosphere and land cover influence on stream water quality in Central Asia's glacierized catchments

This work helps address recent calls for systematic water quality assessment in Central Asia and considers how nutrient and salinity sources, and transport, affect water quality along the continuum from the cryosphere to the lowland plains. Spatial and, for the first time, temporal variations in stream water pH, temperature, electrical conductivity, and nitrate and phosphate concentrations are presented for four catchments (485–13,500 km2), all with glaciers and major urban areas. The catchments studied were: Kaskelen (Kazakhstan), Ala-Archa (Kyrgyzstan), Chirchik (Uzbekistan) and the Kofarnihon (Tajikistan). Measurements were made in cryosphere, stream water, groundwater, reservoir and lake samples over a 22-month period at fortnightly intervals from 35 sites. The results highlight that glacier, permafrost and rock glacier outflows were primary and secondary nitrate sources (>1 mg N L−1) to the headwaters, and there were major increases in salinity and nitrate concentrations where rivers receive inputs from agriculture and settlements. Overall, the water quality complied with national and World Health Organization standards, however there were pollution hot-spots with shallow urban groundwaters contaminated with nitrate (>11 mg N L−1) and stream electrical conductivity above 800 μS cm−1 in some agricultural areas indicative of high salinity. Phosphate concentrations were generally low (<0.06 mg P L−1) throughout the catchments, though elevated (>0.2 mg P L−1) in urban areas due to effluent contamination. A melt water dilution effect along the main river channels was discernible, in the electrical conductivity and nitrate concentration seasonal dynamics, 100 s of km from the headwaters. Thus, the input of relatively clean water from the cryosphere is an important regulator of main channel water quality in the urban and farmed lowland plains adjacent to the Tien Shan and Pamir. Improved sewage treatment is needed in urban areas.

High-efficiency lanthanum-modified zeolite adsorbents for phosphorus control and algal suppression: Preparation, characterization and mechanistic insights

The use of lanthanum (La)-based materials for phosphate removal from water has received increasing attention. However, challenges remain to enhance phosphate (P) sorption capacities and remove P at low concentrations. In this study, lanthanum modified zeolite materials loaded with different lanthanum types were synthesized by hydrothermal method. Based upon preliminary screening of synthesized La-modified zeolite materials in terms of phosphate sorption capacity and La content, lanthanum chloride-modified zeolite (LZ) is chosen for further study. Specifically, for these materials, phosphate sorption kinetics and isotherm behavior, and solution matrix effects (solution pH, and ionic strength) are reported. The developed LZ has a high sorption capacity of 124.38 mg/g, which exceeds that of most La-based adsorbents currently available. P uptake by LZ was pH-dependent with the highest sorption capacities observed over a pH range of 3 ∼ 9. The presence of coexisting ions (Cl-, SO42-, HCO3–) does not significantly affect the adsorption capacity of LZ. In a real treated wastewater effluent with phosphate concentration of 1.92 mg/L and 0.155 mg/L, 0.1 g/L and 0.01 g/L of LZ efficiently reduced the phosphate concentration to below 0.01 mg P/L. Electrostatic attraction and inner-sphere complexation were identified as the sorption mechanisms of phosphate by LZ. The acute toxicity test confirms that the addition of LZ has no acute toxicity effect on aquatic organisms. However, LZ shows indirect and direct inhibitory effects on algae growth, which is beneficial for the control of eutrophic water. Moreover, the exhausted LZ can be easily regenerated with over 70 % adsorption capacity remained during five recycles. Overall, LZ shows great application potential, and this work provides new insights into the molecular-level mechanism of phosphate sequestration by LZ.