Search Results (29)

Nitrogen (N) is a key nutrient for grapevine development, influencing from biomass formation to photosynthetic efficiency and grape quality. However, despite the widespread adoption of grafted plants in modern viticulture, understanding of how different scion–rootstock combinations modulate the uptake of different forms of N present in the soil remains limited. In this context, assessing the nutrient uptake efficiency of grapevines can be a strategy for selecting efficient cultivars, especially in nutritionally poor environments. This study aimed to assess the uptake efficiency of N forms by ‘Chardonnay’ and ‘Cabernet Sauvignon’ grafted onto rootstocks ‘IAC 572’, ‘Paulsen 1103’ and ‘SO4’. Vines were subjected to Hoagland’s nutrient solution at 50% total strength for 21 days, followed by nutrient depletion and a 72 h kinetic uptake assay. Morphological, physiological, biochemical and uptake-related parameters—V_max, K_m, C_min and influx (I)—were assessed. ‘Chardonnay’ grafted onto the ‘IAC 572’ rootstock was the most efficient in the uptake of both NO₃⁻ and NH₄⁺, as it showed the lowest K_m and C_min values and a high influx in relation to the other grapevines evaluated. In general, the ‘Cabernet Sauvignon’ grafted onto the ‘Paulsen 1103’ and ‘IAC 572’ exhibited the highest affinity (i.e., lower K_m) for N forms, indicating that these combinations are more adaptable to environments with low N availability or require lower N inputs. These findings highlight the importance of using kinetic parameters in plant selection, because they can point out the efficient use of and ability to uptake different N forms, in addition to selecting plants that are efficient at uptaking nutrients in nutritionally depleted soils, or even physiologically efficient with low fertilization rates. Full article

Excess phosphorus (P) and nitrogen (N) in wastewater contribute to eutrophication, driving the need for low–cost and sustainable recovery technologies. This study presents a novel adsorbent synthesized from spent coffee grounds biochar (CB) chemically modified with Mn²⁺/Zn²⁺/Fe³⁺ (oxy)hydroxide nanoparticles (CB–M) for simultaneous removal of phosphate and ammonium. Batch adsorption experiments using both synthetic solution and municipal wastewater were conducted to evaluate the material’s adsorption performance and practical applicability. Kinetic, isotherm, thermodynamic, and sequential extraction analyses revealed that CB–M achieved maximum phosphate adsorption capacities ranging from 42.6 to 72.0 mg PO₄³⁻·g⁻¹ across temperatures of 20–33 °C, reducing effluent phosphate concentrations to below 0.01 mg·L⁻¹. Ammonium removal was moderate, with capacities ranging between 2.8 and 2.95 mg NH₄⁺·g⁻¹. Thermodynamic analysis indicated that phosphate adsorption was spontaneous and endothermic, dominated by inner–sphere complexation, while ammonium uptake occurred primarily through weaker, reversible ion exchange mechanisms. Sequential extraction showed over 70% of adsorbed phosphate was associated with Fe-Mn-Zn phases, indicating the potential for use as a slow–release fertilizer. The CB–M retained structural integrity and exhibited partial desorption, supporting its reusability for nutrient recovery. Compared to other biochars, CB–M demonstrated superior phosphate selectivity at a neutral–pH, avoided the use of hazardous metals, and transformed coffee waste into a multifunctional material for wastewater treatment and soil amendment. These findings underscore the potential of CB–M as a circular economy solution for nutrient recovery without introducing secondary contamination. Full article

Chitosan (CS) and polyvinyl alcohol (PVA) nanofiber membranes were synthesized via electrospinning and used as supporting materials for powdered porous organic polymer (POP). These membranes were then crosslinked with glutaraldehyde, resulting in nanofiber membranes (CS/PVA/POP) as an efficient adsorbent for Hg(II) ions. Characterization using Fourier transform infrared spectroscopy, X-ray diffraction, and scanning electron microscopy showed that the membranes effectively removed up to 92.9% of mercury ions at optimal conditions, with an adsorption capacity of 116.1 mg/g. The adsorption data fit well with the Langmuir isotherm and pseudo-second-order kinetic models. The efficient uptake of mercury ions was attributed to chemisorption involving active groups (C=S, -NH₂, -OH), facilitated by mechanisms such as chelation, complexation, or electron exchange. The CS/PVA/POP nanofiber membranes demonstrated significant advantages in adsorption capacity, economic viability, and recyclability, providing an effective solution to mercury pollution in water. Full article

Intensified human activities such as urbanization, agricultural production, industrialization, mining, and fish farming have led to high concentrations of nutrients in water bodies, resulting in eutrophication. Eutrophication has become a global problem that threatens water ecosystems globally. The present study examines the efficiency of applying a novel modified material as an adsorbent for phosphate and ammonium uptake from natural eutrophic freshwater, called ‘ZeoPhos’. The novel material consists of natural zeolite and the addition of iron, calcium, and humic ions, which have been reported for their high adsorption capacity and nutrient-binding properties. Morphological and chemical composition analysis by SEM/EDS and TEM microscopic analysis results are included for natural and modified zeolite. Ammonium and orthophosphate kinetic adsorption results are aligned with pseudo-second kinetic models and reveal 78% and 70% adsorption removal efficiency for solutions of 1 mg NH₄⁺-N/L and 1 mg PO₄³⁻-P/L, respectively. Finally, ‘ZeoPhos’ ammonium and orthophosphate ions adsorption capacity reached up to 28.61 mg/g ± 0.32 and 27.13 mg/g ± 0.57, respectively, after Langmuir fitting isotherm experiments. Full article

Due to the increasing fluoride concentrations in water bodies, significant environmental concerns have arisen. This study focuses on aluminum-based materials with a high affinity for fluorine, specifically enhancing metal–organic frameworks (MOFs) with amino groups to improve their adsorption and defluorination performance. We systematically investigate the factors influencing and mechanisms governing the adsorption and defluorination behavior of amino-functionalized aluminum-based MOF materials in aqueous environments. An SEM, XRD, and FT-IR characterization confirms the successful preparation of NH₂-MIL-101 (Al). In a 10 mg/L fluoride ion solution at pH 7.0, fluoride ion removal efficiency increases with the dosage of NH₂-MIL-101 (Al), although the marginal improvement decreases beyond 0.015 g/L. Under identical conditions, the fluoride adsorption capacity of NH₂-MIL-101 (Al) is seven times greater than that of NH₂-MIL-101 (Fe). NH₂-MIL-101 (Al) demonstrates effective fluoride ion adsorption across a broad pH range, with superior fluoride uptake in acidic conditions. At a fluoride ion concentration of 7 mg/L, with 0.015 g of NH₂-MIL-101 (Al) at pH 3.0, adsorption equilibrium is achieved within 60 min, with a capacity of 31.2 mg/g. An analysis using adsorption isotherm models reveals that the fluoride ion adsorption on NH₂-MIL-101 (Al) follows a monolayer adsorption model, while kinetic studies indicate that the predominant adsorption mechanism is chemical adsorption. This research provides a scientific basis for the advanced treatment of fluoride-containing wastewater, offering significant theoretical and practical contributions. Full article

The uptake of four liposomal formulations was tested with the murine endothelial cell line bEnd.3 and the human glioblastoma cell line U-87 MG. All formulations were composed of DPPC, cholesterol, 5 mol% of mPEG (2000 Da, conjugated to DSPE), and the dye DiD. Three of the formulations had an additional PEG chain (nominally 5000 Da, conjugated to DSPE) with either succinimide (NHS), glucose (PEG-bound at C-6), or 4-aminophenyl β-D-glucopyranoside (bound at C-1) as ligands at the distal end. Measuring the uptake kinetics at 1 h and 3 h for liposomal incubation concentrations of 100 µM, 500 µM, and 1000 µM, we calculated the liposomal uptake saturation S and the saturation half-time t_1/2. We show that only succinimide has an elevated uptake in bEnd.3 cells, which makes it a very promising and so far largely unexplored candidate for BBB transfer and brain cancer therapies. Half-times are uniform at low concentrations but diversify for high concentrations for bEnd.3 cells. Contrary, U-87 MG cells show almost identical saturations for all three ligands, making a uniform uptake mechanism likely. Only mPEG liposomes stay at 60% of the saturation for ligand-coated liposomes. Half-times are diverse at low concentrations but unify at high concentrations for U-87 MG cells. Full article

Using an endogenous carrier is the best method to address the biocompatibility of carriers in the drug delivery field. Herein, we prepared a glutathione-responsive paclitaxel prodrug micelle based on an endogenous molecule of L-glutathione oxidized (GSSG) for cancer therapy using one-pot synthesis. The carboxyl groups in L-glutathione oxidized were reacted with the hydroxyl group in paclitaxel (PTX) using the catalysts dicyclohexylcarbodiimide (DCC) and 4-dimethylaminopyridine (DMAP). Then, the amino-polyethylene glycol monomethyl ether (mPEG-NH₂) was conjugated with GSSG to prepare PTX-GSSG-PEG. The structure of PTX-GSSG-PEG was characterized using infrared spectroscopy (FT-IR), nuclear magnetic resonance spectroscopy (NMR), and mass spectrometry (MS). The drug release kinetics of PTX within PTX-GSSG-PEG were quantified using ultraviolet spectroscopy (UV-Vis). The size of the PTX-GSSG-PEG micelles was 83 nm, as evaluated using dynamic light scattering (DLS), and their particle size remained stable in a pH 7.4 PBS for 7 days. Moreover, the micelles could responsively degrade and release PTX in a reduced glutathione environment. The drug loading of PTX in PTX-GSSG-PEG was 13%, as determined using NMR. Furthermore, the cumulative drug release rate of PTX from the micelles reached 72.1% in a reduced glutathione environment of 5 mg/mL at 120 h. Cell viability experiments demonstrated that the PTX-GSSG-PEG micelles could induce the apoptosis of MCF-7 cells. Additionally, cell uptake showed that the micelles could distribute to the cell nuclei within 7 h. To sum up, with this glutathione-responsive paclitaxel prodrug micelle based on the endogenous molecule GSSG, it may be possible to develop novel nanomedicines in the future. Full article

Ammonium sulfate (AS) has been utilized in agriculture; however, there is a dearth of research on its application in maize cultivation subsequent to the implementation of nitrification inhibitors or coating treatments. This study aimed to analyze the impacts of various combinations of AS fertilizers on soil nutrients, plant nutrient uptake, yield, and fertilizer utilization efficiency in maize cultivation to establish an optimal and stabilized disposal method for AS. A completely randomized design was employed with five treatments (AU, the control using urea; AS, treatment using ammonium sulfate; ASN, treatment using ammonium sulfate with a nitrification inhibitor; ASG, treatment using oil-coated ammonium sulfate; and ASD, treatment using oil–humic acid-coated ammonium sulfate). The results show the following: (1) Compared with AU and AS, ASN, ASG, and ASD decreased the leaching rates of total nitrogen (TN), ammonium nitrogen (NH₄⁺-N), and nitrate nitrogen (NO₃⁻-N), and more residual N had accumulated in the soil. The first-order kinetic equation N_t = N₀(1 − e^−kt) could better fit the process of N accumulation and release, and the N-release rate constant was in the order of AU > CK > AS > ASG > ASN > ASD. (2) Compared with the AU and AS treatments, the plant dry weight, grain dry weight, spike width, spike length, and yields of maize increased by 8.85–11.08%, 12.98–14.15%, 2.95–3.52%, 5.50–5.65%, and 43.21–51.10%, respectively, under the ASG treatment. A path analysis revealed the main decision coefficient of the effective spike number on the maize yield. Furthermore, the accumulation levels of N, P, and K within above-ground plants significantly increased under the ASG treatment compared with those under the AU and AS treatments. N, P, and K partial factor productivity under the ASG treatment increased by 47.12%, 47.15%, and 73.40% on average, while grain N, P, and K balance increased by 50.45%, 47.10%, 55.61% on average, compared with the AU and AS treatments. Therefore, the ASG treatment exhibited the optimal slow-release effect on nutrients and achieved excellent performance in enhancing the production and efficiency of maize. Full article

In coastal lagoons, marine benthic macrophyte meadows can be an important element in the resistance to eutrophication of the ecosystem, as they can function as temporary nitrogen sinks, limiting the availability of this nutrient for opportunistic organisms. The role of nitrogen sinks for two dominant macrophyte species of Mediterranean coastal lagoons, the seagrass Cymodocea nodosa and the seaweed Caulerpa prolifera, was analysed by two different approaches: (i) studying nitrate (NO₃^-) and ammonium (NH₄⁺) uptake kinetics of aboveground tissues in a laboratory and (ii) estimating nitrogen stocks and demands of meadows under natural conditions. The studies were carried out in the coastal lagoon of the Mar Menor, which has been subjected to high anthropogenic nitrogen inputs for decades. While both macrophytes were efficient in exploiting NH₄⁺ from the water column, only C. prolifera showed a high NO₃^- uptake capacity. Large N pools in the C. nodosa and C. prolifera meadows of the Mar Menor were detected, suggesting that these habitats may have the potential to be essential reservoirs for this nutrient. However, the major role of belowground tissues of the seagrasses in nitrogen accumulation may determine important differences between the two species in temporary N storage and sequestration. The data on N demands for the meadows of both macrophytes in the Mar Menor suggest an important contribution of these habitats in controlling the inputs of this nutrient into the lagoon. We conclude that C. nodosa and C. prolifera meadows can play a key role as a sink for dissolved inorganic nitrogen in temperate coastal lagoons, being an important mechanism of resistance to eutrophication. Full article

This study investigated the effects of nitrogen form on root activity and nitrogen uptake kinetics of Camellia oleifera Abel. seedlings, providing a scientific basis for improving nitrogen use efficiency and scientific fertilization in C. oleifera production. Taking one-year-old C. oleifera cultivar ‘Xianglin 27’ seedlings as subjects, 8 mmol·L⁻¹ of nitrogen in varied forms (${\mathrm{NO}}_3^{-}$:${\mathrm{NH}}_4^{+}$ = 0:0, 10:0, 7:3, 5:5, 3:7, 0:10) was applied in this study as the treatment conditions to investigate the effects of different nitrogen forms on root activity and nitrogen uptake kinetics in C. oleifera seedlings. Comparing the performance of nutrient solutions with different ${\mathrm{NO}}_3^{-}$:${\mathrm{NH}}_4^{+}$ ratios, the results showed that a mixed nitrogen source improved the root activity of C. oleifera seedlings based on total absorption area, active absorption area, active absorption area ratio, specific surface area, and active specific surface area. When ${\mathrm{NO}}_3^{-}$:${\mathrm{NH}}_4^{+}$ = 5:5, the total absorption area and active absorption area of the seedling roots reached the maximum. The results of uptake kinetic parameters showed that Vmax ${\mathrm{NH}}_4^{+}$ > Vmax ${\mathrm{NO}}_3^{-}$ and Km ${\mathrm{NO}}_3^{-}$ > Km ${\mathrm{NH}}_4^{+}$, indicating that the uptake potential of ammonium–nitrogen by C. oleifera seedlings is greater than that of nitrate–nitrogen. The conclusion was that compared to either ammonium– or nitrate–nitrogen, the mixed nitrogen source was better for promoting the root activity of C. oleifera seedlings, and the best nitrate/ammonium ratio was 5:5. Full article

Chitosan, a natural organic polymer, has shown bifunctional characteristics in the removal of cationic and anionic contaminants from water and wastewater treatment. In particular, cationic Cu(II) and anionic phosphate can simultaneously interact with chitosan owing to the presence of the amino group in the form of NH₂ and NH₃⁺ in chitosan. To gain greater insight into the bifunctional adsorption characteristics of chitosan, its adsorption capacity for Cu(II) and phosphate was tested under single and mixed (co-ion) conditions to investigate the interactions between four types of chitosan beads and NH₂ and NH₃⁺. In the single condition, Cu(II) uptake was reduced from 0.243 to 0.0197 mmol/g due to the crosslinking and drying processes, whereas no significant reduction in phosphate uptake was observed, indicating that the crosslinking agent only interacted with NH₂ to decrease the number of available adsorption sites for Cu(II). Under the mixed condition, the simultaneous presence of the two ions clearly increased the uptake of each other, with the adsorption of phosphate being more influenced than that of Cu(II). The comparison of the rate constant, k₁ or k₂, using pseudo-first- and pseudo-second-order models confirmed that phosphate reached equilibrium faster than Cu(II), suggesting that electrostatic interaction was preferred over coordination. In addition, under mixed conditions, co-ion competition slowed down the adsorption kinetics for both Cu(II) and phosphate. Full article

Five alkali-activated analcime (ANA) sorbents (ANA-MK 1, ANA 2, ANA 3, ANA-MK 4, and ANA-MK 5) were developed for ammonium (NH₄⁺) ion removal. Acid treatment and calcination were used as pre-treatments for analcime, and metakaolin (MK) was used as a blending agent in three sorbents. Sorption experiments were performed to evaluate the effects of sorbent dosage (1–20 g L⁻¹), initial NH₄⁺ ion concentration (5–1000 g L⁻¹), and contact time (1 min–24 h). ANA-MK 1, ANA 2, and ANA-MK 4 were the most efficient sorbents for NH₄⁺ ion removal, with a maximum experimental sorption uptake of 29.79, 26.00, and 22.24 mg g⁻¹, respectively. ANA 3 and ANA-MK 5 demonstrated lower sorption capacities at 7.18 and 12.65 mg g⁻¹, respectively. The results for the sorption of NH₄⁺ ions onto the alkali-activated analcime surfaces were modeled using several isotherms. The Langmuir, Freundlich, Sips, and Bi-Langmuir isotherms were the best isotherm models to represent the studied systems. The results of the kinetic studies showed the maximum NH₄⁺ ion removal percentage of the sorbents was ~80%, except for ANA-MK 5, which had a ~70% removal. Moreover, the pseudo-first-order, pseudo-second-order, and Elovich models were applied to the experimental data. The results showed that the sorption process for ANA-MK 1, ANA 2, ANA 3, and ANA-MK 4 followed the Elovich model, whereas the pseudo-second-order model provided the best correlation for ANA-MK 5. Full article

Analyzing the molecular and physiological processes that govern the uptake and transport of nitrogen (N) in plants is central to efforts to fully understand the optimization of plant N use and the changes in the N-use efficiency in relation to changes in atmospheric N deposition changes. Here, a field experiment was conducted using the ectomycorrhizal fungi (EMF), Pisolithus tinctorius (Pt) and Suillus grevillei (Sg). The effects of N deposition were investigated using concentrations of 0 kg·N·hm⁻²a⁻¹ (N0), a normal N deposition of 30 kg·N·hm⁻²a⁻¹ (N30), a moderate N deposition of 60 kg·N·hm⁻²a⁻¹ (N60), and a severe N deposition of 90 kg·N·hm⁻²a⁻¹ (N90), with the goal of examining how these factors impacted root activity, root absorbing area, NH₄⁺ and NO₃⁻ uptake kinetics, and the expression of ammonium and nitrate transporter genes in Pinus massoniana seedlings under different levels of N deposition. These data revealed that EMF inoculation led to increased root dry weight, activity, and absorbing area. The NH₄⁺ and NO₃⁻ uptake kinetics in seedlings conformed to the Michaelis–Menten equation, and uptake rates declined with increasing levels of N addition, with NH₄⁺ uptake rates remaining higher than NO₃⁻ uptake rates for all tested concentrations. EMF inoculation was associated with higher V_max values than were observed for non-mycorrhizal plants. Nitrogen addition resulted in the upregulation of genes in the AMT1 family and the downregulation of genes in the NRT family. EMF inoculation under the N60 and N90 treatment conditions resulted in the increased expression of each of both these gene families. NH₄⁺ and NO₃⁻ uptake kinetics were also positively correlated with associated transporter gene expression in P. massoniana roots. Together, these data offer a theoretical foundation for EMF inoculation under conditions of increased N deposition associated with climate change in an effort to improve N absorption and transport rates through the regulation of key nitrogen transporter genes, thereby enhancing N utilization efficiency and promoting plant growth. Synopsis: EMF could enhance the efficiency of N utilization and promote the growth of Pinus massoniana under conditions of increased N deposition. Full article

Ammonium (NH₄⁺), as a major inorganic source of nitrogen (N) for tea plant growth, is transported and distributed across membranes by the proteins of ammonium transporters (AMTs). However, the AMT2-type AMTs from tea plants remain poorly understood. In this study, five CsAMT2 subfamily genes were identified in tea plant genomes, and their full-length coding sequences (CDS) were isolated from roots. Then, a NH₄⁺ uptake kinetic comparison of Fudingdabaicha (FD), Huangdan (HD), and Maoxie (MX) showed that FD was a high N efficiency (HNE) cultivar that had a wide range of adaptability to NH₄⁺, HD was a high N efficiency under high N conditions (HNEH) cultivar, in which it was easy to obtain higher yield in a high N environment, and MX was a high N efficiency under low N conditions (HNEL) cultivar, which had a higher affinity for NH₄⁺ than the other two. Tissue-specific expression analysis suggested that CsAMT2.2 and CsAMT2.3 were highly expressed in the roots, indicating that these two members may be unique in the CsAMT2 subfamily. This is further supported by our findings from the temporal expression profiles in the roots among these three different N adaptation cultivars. Expression levels of CsAMT2.2 and CsAMT2.3 in FD and HD were upregulated by a short time (2 h) under high NH₄⁺ treatment, while under low NH₄⁺ treatment, CsAMT2.2 and CsAMT2.3 were highly expressed at 0 h and 2 h in the HNEL-type cultivar—MX. Furthermore, the functional analysis illustrated that CsAMT2.2 and CsAMT2.3 could make a functional complementation of NH₄⁺-defective mutant yeast cells at low NH₄⁺ levels, and the transport efficiency of CsAMT2.3 was higher than that of CsAMT2.2. Thus, we concluded that CsAMT2.2 and CsAMT2.3 might play roles in controlling the NH₄⁺ uptake from the soil to the roots. These results will further the understanding of the NH₄⁺ signal networks of AMT2-type proteins in tea plants. Full article

This work successfully created a polypyrrole-polyethyleneimine (PPy-PEI) nano adsorbent for the elimination of the lead ion Pb²⁺ from an aqueous solution. An efficient conducting polymer-based adsorbent called as was created using ammonium persulfate (NH4)₂S₂O₈ as an oxidant (PPy-PEI). The PEI hyper-branched polymer with terminal amino groups was added to the PPy adsorbent to offer heavy metals more effective chelating sites. Pb²⁺ removal from aqueous solution using polyethyleneimine micro adsorbent was successfully accomplished using a batch equilibrium technique (PPy-PEI). The generated water-insoluble polymer nanoadsorbent had enough nitrogen atoms; therefore, an effort was made to link PEI, a water-soluble PPy, with PPy, a conjugated polymer, for lead ion adsorption from an aqueous solution. The generated PPy-PEI nanoadsorbents were discovered to have average particle sizes of 18–34 nm and a Brunauer-Emmet-Teller surface area of 17 m²/g, respectively. The thermal behavior of the composites was investigated using thermo gravimetric and differential scanning calorimetric methods. The lead ion adsorption efficacy of pure polypyrrole was found to be 38%; however, a batch equilibrium technique employing nanoadsorbent revealed with the maximum adsorption capacity of 75.60 mg g⁻¹. At pH 10 and 30 min of contact time at 50 °C, 0.2 g of adsorption was shown to be the ideal dosage. X-ray diffraction analysis, energy-dispersive ray spectroscopy, and Fourier transform infrared ray spectrum support the lead ion adsorption by PPy-PEI nanoadsorbents. The cauli-like structure was visible using field emission scanning electron microscopy. Studying the thermodynamic showed that the adsorption was endothermic as illustrated from the positive value of value of ΔH° is 1.439 kJ/mol which indicates that the uptake of Pb²⁺ onto nanoadsorbent PPy-PEI could be attributed to a physical adsorption process. According to the values of ΔG°, the adsorption process was spontaneous at all selected temperatures. The positive value of ΔS° value (43.52 j/mol) suggested an increase in the randomness at the solid/solution interface during the adsorption process. The adsorption data meet the pseudo-second-order kinetic model and suited the Langumuir isothermal model effectively. Full article