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Calcium overload can lead to tumor cell death. However, because of the powerful calcium channel excretory system within tumor cells, simplistic calcium overloads do not allow for an effective antitumor therapy. Hence, the nanoparticles are created with polyethylene glycol (PEG) donor-modified calcium phosphate (CaP)-coated, manganese-doped hollow mesopores Prussian blue (MMPB) encapsulating glucose oxidase (GOx), called GOx@MMPB@CaP-PEG (GMCP). GMCP with a three-mode enhancement of intratumor reactive oxygen species (ROS) levels is designed to increase the efficiency of the intracellular calcium overload in tumor cells to enhance its anticancer efficacy. The released exogenous Ca 2+ and the production of cytotoxic ROS resulting from the perfect circulation of the three-mode ROS outbreak generation that Fenton/Fenton-like reaction and consumption of glutathione from Fe 2+ /Fe 3+ and Mn 2+ /Mn 3+ circle, and amelioration of hypoxia from MMPB-guided and GOx-mediated starvation therapy. Photothermal efficacy-induced heat generation owing to MMPB accelerates the above reactions. Furthermore, abundant ROS contribute to damage to mitochondria, and the calcium channels of efflux Ca 2+ are inhibited, resulting in a calcium overload. Calcium overload further increases ROS levels and promotes apoptosis of tumor cells to achieve excellent therapy., (© 2024 Wiley‐VCH GmbH.)

The widespread environmental contamination resulting from the misuse of tetracycline antibiotics (TCs) has garnered significant attention and study by scholars. Photocatalytic technology is one of the environmentally friendly advanced oxidation processes (AOPs) that can effectively solve the problem of residue of TCs in the water environment. This study involved the synthesis of the heterogeneous magnetic photocatalytic material of CoFe 2 O 4 /NaBiO 3 via the solvothermal method, and it was characterized using different characterization techniques. Then, the photocatalytic system under visible light (Vis) was coupled with peroxymonosulfate (PMS) to explore the performance and mechanism of degradation of tetracycline hydrochloride (TCH) in the wastewater. The characterization results revealed that CoFe 2 O 4 /NaBiO 3 effectively alleviated the agglomeration phenomenon of CoFe 2 O 4 particles, increased the specific surface area, effectively narrowed the band gap, expanded the visible light absorption spectrum, and inhibited recombination of photogenerated electron-hole pairs. In the Vis+CoFe 2 O 4 /NaBiO 3 +PMS system, CoFe 2 O 4 /NaBiO 3 effectively activated PMS to produce hydroxyl radicals (·OH) and sulfate radicals (SO 4 - ). Under the conditions of a TCH concentration of 10 mg/L -1 , a catalyst concentration of 1 g/L -1 and a PMS concentration of 100 mg/L -1 , the degradation efficiency of TCH reached 94% after 100 min illumination. The degradation of TCH was enhanced with the increase in the CoFe 2 O 4 /NaBiO 3 and PMS dosage. The solution pH and organic matter had a significant impact on TCH degradation. Notably, the TCH degradation efficiency decreased inversely with increasing values of these parameters. The quenching experiments indicated that the free radicals contributing to the Vis+CoFe 2 O 4 /NaBiO 3 +PMS system were ·OH followed by SO 4 - , hole (h + ), and the superoxide radical (O 2 - ). The main mechanism of PMS was based on the cycle of Co 3+ and Co 2+ , as well as Fe 3+ and Fe 2+ . The cyclic tests and characterization by XRD and FT-IR revealed that CoFe 2 O 4 /NaBiO 3 had good degradation stability. The experimental findings can serve as a reference for the complete removal of antibiotics from wastewater.

Reducing phosphorus (P) loss from agricultural drainage water is challenging. In this study, we aimed to remove P from agricultural drainage water by developing an integrated sediment interceptor with adsorbent modules filled with Zr/Zn nanocomposite-modified ceramsite (ZMC-interceptor). The results of sequential chemical extraction and 31 P NMR showed that the contents of H 2 O-P (1.15 % of total P), NaHCO 3 -P i (10.48 % of total P), and ortho-P (orthophosphate, 90.6 % of total P) in the sediments of the ZMC-interceptors were higher than those in nearby field soils. The average enrichment ratios of particulate P (PP, >450 nm), medium-colloidal P (MCP, 220-450 nm), fine-colloidal P (FCP, 1-220 nm), and truly dissolved P (Truly DP, <1 nm) in the sediment over the field soil were 1.37, 1.21, 1.70, and 3.01, respectively. No significant differences were found in the sediment P-trapping function with and without ZMC integrated sediment interceptors. However, the ZMC-interceptors remarkably reduced total P (39.7 % for influent concentrations of 0.19-0.68 mg L -1 ) from agricultural drainage water compared to those unmodified ceramsite-interceptors (21.7 % for influent concentrations of 0.17-0.66 mg L -1 ) during the drainage 'window period' (June-August 2022). This was mainly due to the higher removal efficacies of MCP (19.7 %), FCP (23.3 %), and Truly DP (34.8 %) of the ZMC-interceptors. This study highlighted that the ZMC-interceptor not only trapped P in the sediment but also facilitated the removal of different-sized P fractionated from agricultural drainage water., Competing Interests: Declaration of competing interest The authors declare that they have no competing financial interests that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Background: Chemodynamic therapy (CDT) is a new treatment approach that is triggered by endogenous stimuli in specific intracellular conditions for generating hydroxyl radicals. However, the efficiency of CDT is severely limited by Fenton reaction agents and harsh reaction conditions., Methods: Bimetallic PtMn nanocubes were rationally designed and simply synthesized through a one-step high-temperature pyrolysis process by controlling both the nucleation process and the subsequent crystal growth stage. The polyethylene glycol was modified to enhance biocompatibility., Results: Benefiting from the alloying of Pt nanocubes with Mn doping, the structure of the electron cloud has changed, resulting in different degrees of the shift in electron binding energy, resulting in the increasing of Fenton reaction activity. The PtMn nanocubes could catalyze endogenous hydrogen peroxide to toxic hydroxyl radicals in mild acid. Meanwhile, the intrinsic glutathione (GSH) depletion activity of PtMn nanocubes consumed GSH with the assistance of Mn 3+ /Mn 2+ . Upon 808 nm laser irradiation, mild temperature due to the surface plasmon resonance effect of Pt metal can also enhance the Fenton reaction., Conclusion: PtMn nanocubes can not only destroy the antioxidant system via efficient reactive oxygen species generation and continuous GSH consumption but also propose the photothermal effect of noble metal for enhanced Fenton reaction activity., Competing Interests: The authors report no conflicts of interest in this work., (© 2024 Wang et al.)

Understanding the behavior of colloidal phosphorus (P coll ) under anoxic conditions is pivotal for addressing soil phosphorus (P) mobilization and transport and its impact on nutrient cycling. Our study investigated P coll dynamics in acidic floodplain soil during a 30-day flooding event. The sudden oxic-to-anoxic shift led to a significant rise in pore-water P coll levels, which exceeded soluble P levels by more than 2.7-fold. Colloidal fractions transitioned from dispersed forms (<220 nm) to colloid-associated microaggregates (>220 nm), as confirmed by electron microscopy. The observed increase in colloidal sizes was paralleled by their heightened ability to form aggregates. Compared to sterile control conditions, anoxia prompted the transformation of initially dispersed colloids into larger particles through microbial activity. Curiously, the 16S rRNA and ITS microbial diversity analysis indicated that fungi were more strongly associated with anoxia-induced colloidal release than bacteria. These microbially induced shifts in P coll lead to its higher mobility and transport, with direct implications for P release from soil into floodwaters.

Colloidal phosphorus (P) is an important P form in agricultural runoff and can threaten water quality. However, up to date, there are few effective approaches to mitigate colloidal P pollution. This study investigated the effect of ultraviolet (UV) irradiation on medium-colloidal (MC; 220 nm-450 nm) and fine-colloidal (FC; 3 kDa-220 nm) P in agricultural runoff. Under 24 h of UV irradiation, as the most abundant colloidal P fraction, concentration of total P (TP) in FC consistently decreased by 81.0%, while TP concentration in MC first increased by 74.4% after 3 h and then decreased with irradiation time. At the same time, particulate TP (>450 nm) concentration was found to be increased from 0 to 14.7 μM. However, there were no obvious variations in TP concentrations in FC and MC fractions under dark conditions. In FC fraction, with the decrease of TP, the corresponding concentrations of iron (Fe), aluminum (Al), silicon (Si) declined synchronously, and ferric iron/ferrous iron (Fe(III)/Fe(II)) ratio and organic matter (OM) concentration were reduced as well. These results suggested that P in FC fraction was gradually transformed into particulate P during photoreduction of Fe(III) and photodegradation of OM under UV irradiation. Our study helps to understand the mechanism of the phototransformation of colloidal P, and propose an UV irradiation-based approach to remove colloidal P in agricultural runoff., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Biodegradable silicate nanoconstructs have aroused tremendous interest in cancer therapeutics due to their variable framework composition and versatile functions. Nevertheless, low intratumoral retention still limits their practical application. In this study, oxygen vacancy (OV)-enriched bimetallic silicate nanozymes with Fe-Ca dual active sites via modification of oxidized sodium alginate and gallic acid (GA) loading (OFeCa SA -V@GA) were developed for targeted aggregation-potentiated therapy. The band gap of silica markedly decreased from 2.76 to 1.81 eV by codoping of Fe 3+ and Ca 2+ , enabling its excitation by a 650 nm laser to generate reactive oxygen species. The OV that occurred in the hydrothermal synthetic stage of OFeCa SA -V@GA can anchor the metal ions to form an atomic phase, offering a massive fabrication method of single-atom nanozymes. Density functional theory results reveal that the Ca sites can promote the adsorption of H 2 O 2, and Fe sites can accelerate the dissociation of H 2 O 2 , thereby realizing a synergetic catalytic effect. More importantly, the targeted delivery of metal ions can induce a morphological transformation at tumor sites, leading to high retention (the highest retention rate is 36.3%) of theranostic components in tumor cells. Thus, this finding may offer an ingenious protocol for designing and engineering highly efficient and long-retention nanodrugs.

The impact of drying-rewetting (DRW) cycles on soil phosphorus (P) behavior is well-established; however, its impact on the different-sized colloidal P (CP) in agricultural soils is still unclear. To investigate the effect of DRW events on the mobilization of CP in agricultural soils, and to understand how this impact varies with different DRW cycles and drought intensities, the study explored the role of soil type, CP fractions, and compositions. The concentration of CP was measured in paddy soil and vegetable soil after 3, 6, and 9 DRW cycles of varying intensities. The CP was then fractionated into fine-sized colloids (FC-P; 1-220 nm), medium-sized colloids (MC-P; 220-450 nm), and coarse-sized colloids (CC-P; 450-1000 nm) through soil supernatant filtration. CP accounted for 71.1 % and 55.6 % of water-dispersible colloidal P (<1000 nm) in paddy and vegetable soils, with FC-P constituting the greatest proportion at 50 % and 44 % of CP respectively. The colloidal fraction correlated with organic carbon, aluminum, and iron. DRW cycles did not change the overall distribution of the three CP size fractions. However, they affected the concentration and composition of CP. This study concluded that DRW can have significant implications for nutrient release and water quality in agricultural soils and that maintaining soil moisture at 50 % to 70 % of water-holding capacity could alleviate CP accumulation resulting from DRW cycles., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

In the context of aquatic environmental issues, dynamic analysis of nano-sized inorganic water pollutants has been one of the key topics concerning their seriously amplified threat to natural ecosystems and life health. Its ultimate challenge is to reach a single-entity level of identification especially towards substantial amount of inorganic pollutants formed as natural or manufactured nanoparticles (NPs), which enter the water environments along with the potential release of constituents or other contaminating species that may have coprecipitated or adsorbed on the particles' surface. Here, we introduced a 'nano-impacts' approach-single entity collision electrochemistry (SECE) promising for in-situ characterization and quantification of nano-sized inorganic pollutants at single-entity level based on confinement-controlled electrochemistry. In comparison with ensemble analytical tools, advantages and features of SECE point at understanding 'individual' specific fate and effect under its free-motion condition, contributing to obtain more precise information for 'ensemble' nano-sized pollutants on assessing their mixture exposure and toxicity in the environment. This review gives a unique insight about the single-entity collision measurements of various inorganic water pollutants based on recent trends and directions of state-of-the-art single entity electrochemistry, the prospects for exploring nano-impacts in the field of inorganic water pollutants measurements were also put forward., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023. Published by Elsevier Ltd.)

Colloidal phosphorus (CP) has high mobility and great loss risk; their biogeochemical processes are influenced by agricultural management such as redox oscillation and biochar-amendment application. This study monitored CP concentration in pore-water, soil P species and P adsorption capacity, to investigate CP release from paddy soils as affected by the interactive effects of oxygen status (continuous anoxic/oxic for 12 days, CA/CO; intermittent anoxic for 2, 4, 6, 8, 10 days during the 12-day cycle, IA 2 - 10 ) and management (soil only, CK; bulk/micro/nano-sized biochar with various properties: SB Bulk , SB Micro , and SB Nano ). Compared to the control (0.25-0.84 mg L -1 , CK-CA), the single intermittent anoxic treatment (CK-IA) reduced CP concentrations by 45 %, due to the rise of Eh and pH and the decline of the degree of P saturation along with the increased soil Fe/Al-P and organic-P. Longer anoxic duration under the CK-IA reduced CP release, probably donated from massive production of redox-stable amorphous Fe/Al-bound P. The single biochar treatment (SB-CA: SB Bulk -CA > SB Micro -CA > SB Nano -CA) decreased CP release by 37 % as compared to the CK-CA, ascribed to the increased soil pH, Eh, and P adsorption capacity. The combined treatment (SB-IA: SB Bulk -IA 2  > SB Nano -IA 10 ) synergistically reduced CP release by 68 % in comparison with the CK-CA, due to the increase of adsorption through interactions of soil Fe/Al/Ca- and organic-P. Therefore, nano-sized biochar and long intermittent anoxic duration are recommended for reducing CP release from paddy soils., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

The clinical application of reactive oxygen species (ROS)-mediated tumor treatment has been critically limited by inefficient ROS generation. Herein, we rationally synthesized and constructed the three-dimensional PdMo nanoflowers through a one-pot solvothermal reduction method for elaborately regulated peroxidase-like enzymatic activity and glutathione peroxidase-like enzymatic activity, to promote oxidation ROS evolvement and antioxidation glutathione depletion for achieving intensive ROS-mediated tumor therapy. The three-dimensional superstructure composed of two-dimensional nanosheet subunits can solve the issues by avoiding the appearance of tightly stacked crystalline nanostructures. Significantly, Mo is chosen as a second metal to alloy with Pd because of its more chemical valence and negative ionization energy than Pd for improved electron transfer efficiencies and enhanced enzyme-like activities. In addition, the photothermal effect generated by PdMo nanoflowers could also enhance its enzymatic activities. Thus, this work provides a promising paradigm for achieving highly ROS-mediated tumor therapeutic efficacy by regulating the multi-enzymatic activities of Pd-based nanoalloys., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2023 Liang, Tang, Kurboniyon, Luo, Tu, Xia, Ning, Zhang and Wang.)

Developing metal-based nanocomposites as adsorbent for phosphorus (P) removal is a simple and effective strategy, while the separation of nanoscale adsorbents from water after adsorption is a tedious job. In this work, a novel Zr/Zn nanocomposite (Zr/Zn NCs) modified ceramsite (ZZMC) was synthesized to enhance P removal from agricultural drainage water. Characterization results showed that Zr/Zn NCs with fusiform nanostructures were uniformly loaded on the ceramsite, hence depending on the high mechanical strength and large size of ceramsite, the Zr/Zn NCs can be conveniently handled and separated after adsorption with P. The common issues of weak adsorption capacity and short using life related to ceramsite for P removal in wastewater were also significantly improved in complementarity combination with Zr/Zn NCs. The ZZMC exhibited higher P removal efficiency (>90%) at 5 mg-P L -1 in a wide pH range (5-9) than bulk ceramsite (<10%) and performed well when other ions were co-existed. For two real agricultural drainage water samples with total phosphorus (TP) of 0.526 mg-P L -1 and 0.865 mg-P L -1 , the ZZMC demonstrated desirable adsorption performance not only for truly dissolved P (<3 kDa; >85%), but also for fine colloidal P (3 kDa-220 nm; 76.1%-79.1%) and medium colloidal P (220-450 nm; 80.7%-82.2%) within 30 adsorption cycles that included two-time regeneration treatments towards this material. Moreover, the adsorption capacity of TP by ZZMC after two regenerated treatments was more than 90% of that of fresh ZZMC. The results revealed the feasibility to remove different-sized P at low concentration for agricultural drainage water by ZZMC., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

The bioavailability for varied-size phosphorus (P)-binding colloids (P coll ) especially from external P sources in soil terrestrial ecosystems remains unclear. This study evaluated the differential contribution of various-sized biogas slurry (BS)-derived colloids to plant available P uptake in the rhizosphere and the corresponding patterns of phosphatase response. Keeping the same content of total P input (15 mg kg -1 ), we applied different size-fractioned BS-derived colloids including nanosized colloids (NCs, 1-20 nm), fine-sized colloids (FCs, 20-220 nm), and medium-sized colloids (MCs, 220-450 nm) respectively to conduct a 45-day rice ( Oryza sativa L. ) rhizotron experiment. During the whole cultivation period, the dynamics of chemical characteristics and P fractions in each experimental rhizosphere soil solution were analyzed. The spatial and temporal dynamics examination of P-transforming enzymes (acid phosphatases) in the rice rhizosphere was visualized by a soil zymography technique after 5, 25, and 45 days of rice transplantation. The results indicated that the acid phosphatase activities and its hot spot areas were significantly 1) correlated with the relative bioavailability of colloidal P (RBA coll ), 2) increased with the colloid-free (truly dissolved P) and BS-derived NC addition, and 3) affected by the plant growth stage. With the nanosized BS colloid addition, the RBA coll and plant biomass were respectively found to be the highest (64% and 1.22 g plant -1 ), in which the acid phosphatase-catalyzed hydrolysis of organic P coll played an important role. All of the above suggested that nanosized BS-derived colloids are an effective alternative to conventional phosphorus fertilizer for promoting plant P uptake and P bioavailability.

Traditional treatment methods for tumors are inefficient and have severe side effects. At present, new therapeutic methods such as phototherapy, chemodynamic therapy, and gasodynamic therapy have been innovatively developed. High concentrations of hydrogen sulfide (H 2 S) gas exhibit cancer-suppressive effects. Herein, a Prussian blue-loaded tetra-sulfide modified dendritic mesoporous organosilica (PB@DMOS) was rationally constructed with glutathione (GSH)-triggered/photothermal-enhanced H 2 S signaling molecule release properties for gas therapy. The as-synthesized nanoplatform confined PB nanoparticles in the mesoporous structure of organosilica silica due to electrostatic adsorption. In the case of a GSH overexpressed tumor microenvironment, H 2 S gas was controllably released. And the temperature increases due to the photothermal effects of PB nanoparticles, further enhancing H 2 S release. At the same time, PB nanoparticles with excellent hydrogen peroxide catalytic performance also amplified the efficiency of tumor therapy. Thus, a collective nanoplatform with gas therapy/photothermal therapy/catalytic therapy functionalities shows potential promise in terms of efficient tumor therapy.

Soil water-dispersible colloidal phosphorus (WCP) presents high mobility, however, the regulatory effect of biochar-coupled organic fertilizer is rarely known, especially under different cropping patterns. This study investigated the P adsorption, soil aggregate stability, and WCP in three paddy and three vegetable fields. These soils were amended with different fertilizers (chemical fertilizer, CF; substitution of solid-sheep manure or liquid-biogas slurry organic fertilizer, SOF/LOF; substitution of biochar-coupled organic fertilizers, BSOF/BLOF). Results presented that the LOF averagely increased the WCP contents by 50.2% across the sites, but the SOF and BSOF/BLOF averagely decreased their contents by 38.5% and 50.7% in comparison with the CF. The WCP decline in the BSOF/BLOF-amended soils was mainly attributed to the intensive P adsorption capacity and soil aggregate stability. The BSOF/BLOF increased the amorphous Fe and Al contents in the fields in comparison with the CF, which improved the adsorption capacity of soil particles, further improving the maximum absorbed P (Q max ) and reducing the dissolved organic matter (DOC), leading to the improvement of > 2 mm water-stable aggregate (WSA >2mm ) and subsequent WCP decrease. This was proved by the remarkable negative associations between the WCP and Q max (R 2  = 0.78, p < 0.01) and WSA >2mm (R 2  = 0.74, p < 0.01). This study manifests that biochar-coupled organic fertilizer could effectively reduce soil WCP content via the improvement of P adsorption and aggregate stability., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Hyperthermia therapy is a hotspot because of its minimally invasive treatment process and strong targeting effect. Herein, a synergistic magnetic and photothermal therapeutic nanoplatform is rationally constructed. The well-dispersive mSiO 2 -SmCo x nanoparticles (NPs) were synthesized through a one-step procedure with the regulated theoretical molar ratio of Sm/Co among 1:1, 1:2, and 1:4 for controlling the dispersion and magnetism properties of SmCo x NPs in situ growth in the pore structure of mesoporous SiO 2 (mSiO 2 ), where mSiO 2 with diverse porous structures and high specific surface areas serving for locating the permanent magnetic SmCo x NPs. The mSiO 2 -SmCo x (Sm/Co = 1:2) NPs with highly dispersed and uniform morphology has an average diameter of ∼73.08 nm. The photothermal conversion efficiency of mSiO 2 -SmCo x (Sm/Co = 1:2) NPs was determined to be nearly 41%. The further in vitro and in vivo anti-tumor evaluation of mSiO 2 -SmCo x (Sm/Co = 1:2) NPs present promising potentials for hyperthermia-induced tumor therapy due to magnetic and photothermal effects., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2023 Liang, Xu, Li, Kurboniyon, Huang, Xu, Wei, Ning, Zhang and Wang.)

Introduction: Reactive oxygen species (ROS)-mediated therapies have typically been considered as noninvasive tumor treatments owing to their high selectivity and efficiency. However, the harsh tumor microenvironment severely impairs their efficiency. Methods: Herein, the biodegradable Cu-doped zeolitic imidazolate framework-8 (ZIF-8) was synthesized for loading photosensitizer Chlorin e6 (Ce6) and CaO 2 nanoparticles, followed by surface decoration by hyaluronic acid (HA), obtaining HA/CaO 2 -Ce6@Cu-ZIF nano platform. Results and Discussion: Once HA/CaO 2 -Ce6@Cu-ZIF targets tumor sites, the degradation of Ce6 and CaO 2 release from the HA/CaO 2 -Ce6@Cu-ZIF in response to the acid environment, while the Cu 2+ active sites on Cu-ZIF are exposed. The released CaO 2 decompose to generate hydrogen peroxide (H 2 O 2 ) and oxygen (O 2 ), which alleviate the insufficiency of intracellular H 2 O 2 and hypoxia in tumor microenvironment (TME), effectively enhancing the production of hydroxyl radical (•OH) and singlet oxygen ( 1 O 2 ) in Cu 2+ -mediated chemodynamic therapy (CDT) and Ce6-induced photodynamic therapy (PDT), respectively. Importantly, Ca 2+ originating from CaO 2 could further enhance oxidative stress and result in mitochondrial dysfunction induced by Ca 2+ overloading. Conclusion: Thus, the H 2 O 2 /O 2 self-supplying and Ca 2+ overloading ZIF-based nanoplatform for cascade-amplified CDT/PDT synergistic strategy is promising for highly efficient anticancer therapy., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2023 Liang, Cai, Tang, Su, Xie, Li and Liang.)

Combined application of biochar and organic fertilizer improves soil structure and crop yield but may lead to increased loss of phosphorus (P). To reduce the P loss risk in this case, rice straw biochar (BC) and sheep manure (SM) were modified using polyacrylamide (PAM). The effects of using organic amendments (BC, SM, and PAM-modified organic mixtures) and no amendments (CK) on soil total and colloidal P leaching loss from paddy soils were evaluated through soil column leaching experiments. The soil leachate volume was increased by 8.91% with BC treatment and reduced by 15.3% with SM treatment. The total P leaching loss (973.9 μg kg -1 ) from the BC-treated soil was higher than that from other treatments (541.4-963.5 μg kg -1 ). However, there was much more colloidal P loss (480.0 μg kg -1 ) from SM treatment. The optimal conditions for the preparation of BC and SM modified using polyacrylamide (PSB) for reducing P leaching loss were SM/BC = 4:1, 1% PAM, and 100 °C. Molybdate-unreactive P accounts for 58.61-86.89% of the colloidal P in the soil leachate with organic amendments. PSB reduced colloidal P loss (particularly in 10-220 nm range) by ~ 50% compared with BC and SM treatments. The colloidal P concentration in the leaching solutions was significantly correlated with TOC and susceptible to Fe and Al concentrations. Using PAM-modified mixture instead of manure and biochar as a soil amendment can effectively control P leaching from fields., (© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

Phosphorus (P) availability and loss risk are linked to P species; however, their alternations in the soil amended with biochar-blended organic fertilizer is not well known, particularly under contrasting soil properties and land management. In this study, the variance of soil P species extracted by sequential chemical extraction (SCE) and 31 P NMR techniques, as well as the degree of P saturation (DPS), were investigated throughout three paddy and three vegetable fields. These fields were amended with three different fertilizers at the same P application rate: chemical fertilizer (CF), organic fertilizer substitution (sheep manure/biogas slurry, SM/BS), and biochar-blended organic fertilizer substitution (BSM/BBS). Results showed that the BSM/BBS and SM increased the total P contents by 7.5% and 5.9% (TP) and available P contents by 30.1% and 19.2% (AP), but decreased the DPS values by 19.4% and 11.7%, compared to the CF treatment. Yet, the BS decreased the TP and AP contents but increased the DPS values across the experimental sites. In the BSM/BBS amended soils, high AP contents were due to the increased inorganic P (NaHCO 3 -P i ), while the increased organic P (monoester and DNA) induced low DPS values and reduced soil P loss risk. Our study highlights that biochar-blended organic fertilizer is an effective agronomic way for improving P availability and decreasing P loss risk via the alteration of soil P species., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Soil colloids have been shown to play a critical role in soil phosphorus (P) mobility and transport. However, identifying the potential mechanisms behind colloidal P (P coll ) release and the key influencing factors remains a blind spot. Herein, a machine learning approach (random forest (RF) coupled with partial dependence plot analyses) was applied to determine the effects of different soil physicochemical parameters on P coll content in three colloidal subfractions (i.e., nano- (NC): 1-20 nm, fine- (FC): 20-220 nm and medium-sized colloids (MC): 220-450 nm) based on a regional dataset of 12 farmlands in Zhejiang Province, China. RF successfully predicted P coll content (R 2  = 0.98). Results showed that colloidal- organic carbon (OC coll ) and minerals were the major determinants of total P coll content (1-450 nm); their critical values for increasing P coll release were 87.0 mg L -1 for OC coll , 11.0 mg L -1 for iron (Fe coll ) or aluminium (Al coll ), 2.6 mg L -1 for calcium (Ca coll ), 9.0 mg L -1 for magnesium (Mg coll ), 2.5 mg L -1 for silicon (Si coll ), and 1.4 mg L -1 for manganese (Mn coll ). Among three colloidal subfractions, the major factors determining P coll were soil Olsen-P (P Olsen ; 125.0 mg kg -1 ), Ca coll (2.5 mg L -1 ), and colloidal P saturation (21.0%) in NC; Mn coll (1.5 mg L -1 ), Mg coll (6.8 mg L -1 ), and P Olsen (135.0 mg kg -1 ) in FC; while Mn coll (1.5 mg L -1 ), Al coll (2.5 mg L -1 ), and Fe coll (3.8 mg L -1 ) in MC, respectively. OC coll had a considerable effect in the three fractions, with critical values of 80.0 mg L -1 in NC or FC, and 50.0 mg L -1 in MC. Our study concluded that the information gleaned using the RF model can be used as crucial evidence to identify the key determinants of different size fractionated P coll contents. However, we still need to discover one or more easy-to-measure parameters that can help us better predict P coll ., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

Mobile colloids impact phosphorus (P) binding and transport in agroecosystems. However, their relationship to P-lability and their relative importance to P-bioavailability is unclear. In soils amended with organic fertilisers, we investigated the effects of nano (NC; 1-20 nm), fine (FC; 20-220 nm), and medium (MC; 220-450 nm) colloids suspended in soil solution on soil P-desorption and lability. The underlying hypothesis is that mobile colloids of different sizes, i.e., NC, FC, and MC, may contribute differently to P-lability in soils enriched with organic fertiliser. NC- and FC-bound P coll were positively correlated with P-lability parameters from diffusive gradient in thin films (DGT A -labile P concentration, r ≥ 0.88; and DGT A -effective P concentration, r ≥ 0.87). The corresponding relations with MC-bound P coll are weaker (r values of 0.50 and 0.51). NC- and FC-bound P coll were also strongly correlated with soil P-resupply (r ≥ 0.64) and desorption (r ≥ 0.79) parameters during DGT A deployment, and the mobility of these colloids was corroborated by electron microscopy of DGT A gels. MC-bound P coll was negatively correlated with the solid-to-solution distribution coefficient (r = -0.42), indicating this fraction is unlikely to be the source of P-release from the solid phase after P-depletion from the soil solution. We conclude that NC and FC mainly contribute to regulating soil desorbable-P supply to the soil solution in the DGT A depletion zone (in vitro proxy for plant rhizosphere), and consequently may act as critical conditioners of P-bioavailability, whereas MC tends to form complexes that lead to P-occlusion rather than lability., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Colloidal phosphorus (P coll ) in paddy soils can pose a serious threat to the water environment. Biochar amendment not only directly absorb P coll to reduce the runoff loss, but also create hotspots for microbial communities which simultaneously affects soil P coll . However, despite the crucial role of microorganisms, it remains elusive regarding how biochar and its feedstock types affect the relationships of soil microbial communities and P coll in soil matrix (such as at soil aggregate level). To address the knowledge gap, we explored the (in)direct effects of biochar on the soil P coll in physically separated fractions including micro- (53-250 μm) and macroaggregates (250-2000 μm). Results showed that straw and manure biochars decreased the soil P coll content by 55.2-56.7% in microaggregates and 41.2-48.4% in macroaggregates after 120 days of incubation, compared to the respective control. The fungal communities showed a significantly correlation (0.34, p < 0.05) with P coll content in the macroaggregates, whereas the bacterial communities were extremely significantly correlated (0.66, p < 0.001) with P coll content in the microaggregates. Furthermore, the partial least squares path model analysis indicated that biochar amendments directly increased P coll content (0.76 and 0.61) in micro- and macroaggregates, but the reduced P coll content by biochar was mainly derived from indirect effects, such as changed soil biological characteristics carbon (C)/P (-0.69), microbial biomass C (-0.63), microbial biomass P (-0.68), keystone taxa Proteobacteria (-0.63), and Ascomycota (-0.59), particularly for the macroaggregates. This study highlights that to some extent, biochar addition can reduce soil P coll content by affecting microbial communities (some keystone taxa), and soil biological characteristics at soil aggregate level., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

The manure fertilizer increases the phosphorus (P) saturation of soils and the colloidal P release to water bodies. Manure of different particle-sizes may have different effects on colloidal P release by soil, and to date there is limited knowledge on colloidal P release from soils amended with different size manures. We produced sheep micro- (S Micro ) and nano-manure (S Nano ), and poultry micro- (P Micro ), nano-manure (P Nano ) from bulk samples by wet fractionation method. The fractionation reduced the P contents of micro- and nano-manures, and enriched them in ash and calcium, iron (Fe), magnesium, and aluminum (Al) phosphate minerals compared with the bulk manures. The degree of P saturation (DPS) in Anthorsol and Cambisol was decreased (S Micro , 17.6 and 17.2 %; S Nano , 14.5 and 13.3 % and P Micro , 19.0 and 19.7 mg kg -1 ; P Nano , 17.0 and 14.3 mg kg -1 ) and released less colloidal P (S Micro , 3.12 and 3.78 mg kg -1 ; S Nano , 3.01 and 3.56 mg kg -1 and P Micro , 3.34 and 3.92 mg kg -1 ; P Nano , 3.21 and 3.65 mg kg -1 ) than the soils receiving the bulk manures. The decrease in colloidal P was correlated with less DPS in both soils amended with micro and nano manures. That is, the only measurable effect of manure particle size on colloidal P release from the amended soils was due to chemical fractionation during separation of the size fractions. It was suggested that nano and micro manures were the effective approach to reduce colloidal P release from manure amended soils., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Aberrant expression of genes contributes to the chemoresistance of colorectal cancer (CRC) treatment. This study aimed to identify genes associated with the chemoresistance of oxaliplatin-based chemotherapy in CRC patients and to construct a signature. Oxaliplatin resistance-related genes were screened by analyzing the gene profiles of cell lines and tissue samples that underwent oxaliplatin-based treatment. Oxaliplatin resistance-related genes were used to establish a signature. The association of the signature had clinical significance, so the prognostic value of the signature was analyzed. Independent cohorts and CRC cell lines were used to validate the value of the gene signature and the oxaliplatin-resistant genes. There were 64 oxaliplatin resistance-related genes identified after overlapping the genes from the dataset of oxaliplatin-treated CRC cells and the dataset of patients treated with oxaliplatin-based chemotherapy. A gene signature based on five oxaliplatin resistance-related genes was established. This gene signature effectively predicted the prognosis of CRC patients who underwent chemotherapy. No significant associations were found between the gene mutations and survival of the patients; however, two genes were associated with microsatellite instability status. Two external independent cohorts and CRC cell line experiments validated the prognostic values of the signature and expression of the genes after oxaliplatin treatment. In conclusion, the oxaliplatin resistance-related gene signature involving five genes was a novel biomarker for the prediction of the chemotherapy response and prognosis of CRC patients who underwent oxaliplatin-based chemotherapy.

Developing effective modification methods and obtaining a comprehensive understanding of adsorption mechanisms are essential for the practical application of biochars for the removal of heavy metals from solutions. In this study, rice straw was impregnated with sodium phytate and pyrolyzed at 350 °C, 450 °C, and 550 °C to synthesize modified biochars (i.e., MBC350, MBC450, and MBC550). The Cd(II) adsorption capacities and contributions of different mechanisms, including the effects of biochar-derived dissolved organic matter (BDOM), were investigated using batch sorption experiments and characterization analyses. The modification of sodium phytate promoted the pyrolysis of biomass, thereby increasing the BDOM content and aromatic structures at low and high pyrolysis temperatures, respectively. Moreover, the modification also increased the exchangeable Na + and carbonate contents in the modified biochars. Compared with the raw biochars, the Cd(II) adsorption capacities of modified biochars increased by 3.3-4.3 times, and MBC550 had the highest Cd(II) adsorption capacity (126.5 mg/g), of which precipitation with minerals and interaction with π-electrons contributed 41.7% and 45.8%, respectively. However, at a lower pyrolysis temperature, the Cd(II) adsorption attributed to ion exchange and co-deposition with BDOM significantly increased, especially on MBC350 (33.9 and 12.6 mg/g, respectively). These results indicate that modification by sodium phytate effectively enhanced various adsorption mechanisms, thereby increasing the Cd(II) adsorption capacity. In addition, the contribution of co-deposition with BDOM to adsorption was unneglectable for the biochars pyrolyzed at low temperatures., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Nutrient fertilization plays a major role in improving crop productivity and maintaining soil fertility. In the last few decades, the productivity of current agricultural practices highly depends on the use of chemical fertilizers. Major drawback of traditional fertilizers is their low crop nutrient use efficiency and high loss into water. Nanomaterial in agriculture is a multipurpose tool for increasing growth, development, and yield of plants. Nanotechnology facilitates the amplifying of agriculture production by reducing relevant losses and improving the input efficiency. Nanotechnology has emerged as an attractive field of research and has various agriculture applications, especially the use of nano-agrochemicals to increase nutrient use efficiency and agricultural yield. Nanofertilizers are more effective as compared to chemical fertilizers due to their cost-efficient, eco-friendly, non-toxic, and more stable in nature. Overall, this chapter focuses on synthesis of nanofertilizers through physical, chemical, and biological methods. This chapter will also explore the use of nano-enabled fertilizers to enhance the nutrient use efficiency for sustainable crop production, and global food safety., (© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

The agricultural use of manure fertilizer increases the phosphorus (P) saturation of soils and the risk of colloidal P (P coll ) release to aquatic ecosystems. Two experiments were conducted to identify whether Pteris vittata plantation can decrease P coll contents in two soils (Cambisol and Anthrosol) amended with various manure P rates (0, 10, 25, and 50 mg P kg -1 of soil). The total P coll contents in manured soil without P. vittata were 1.14-3.37 mg kg -1 (Cambisol), and 0.01-2.83 mg kg -1 (Anthrosol) across manure-P rates. The corresponding values with P. vittata were 0.97-2.33 mg kg -1 (Cambisol) and 0.005-1.6 mg kg -1 (Anthrosol). Experimentally determined colloidal minerals (Fe, Al, Ca), colloidal total organic carbon, Mehlich-3 nutrients (Fe, Al, and Ca), and the degree of P saturation were good predictors of P coll concentrations in both soils with and without P. vittata plantation. In unplanted soils, P adsorption decreased and the degree of P saturation increased which released more P coll . However, P. vittata plantation decreased the P coll release and P loss risk due to the increase of P adsorption and reduced DPS in both soils. The P fractions (NaOH, NH 4 F, and HCl-P) contributed to increase the P pool in planted soils which enhanced the bioavailability of P coll and increased the P. vittata biomass. It suggested that P. vittata plantation was an effective approach to reduce P coll release from manure amended soils., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Phosphorus (P) is limiting nutrient in many soils, and P availability may often depend on iron (Fe) speciation. Colloidal iron phosphate (FePO 4coll ) is potentially present in soils, and we tested the hypothesis that phytate exudation by Pteris vittata might dissolve FePO 4coll by growing the plant in nutrient solution to which FePO 4coll was added. The omission of P and Fe increased phytate exudation by P. vittata from 434 to 2136 mg kg -1 as the FePO 4coll concentration increased from 0 to 300 mM. The total P in P. vittata tissue increased from 2880 to 8280 mg kg -1 , and the corresponding increases in the trichloroacetic acid (TCA) extractable P fractions were inorganic P (860-5100 mg kg -1 ), soluble organic P (250-870 mg kg -1 ), and insoluble organic P (160-2030 mg kg -1 ). That is, FePO 4 -solubilizing activity was positive correlated with TP, TCA P fractions in P. vittata, TP in growth media, and root exudates. This study shows that phytate exudation dissolved FePO 4coll due to the chelation effect of phytic acid on Fe; however, the wider question of whether phytic acid excretion was prompted by deprivation of P, Fe, or both remains to be answered., (© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

Phosphate as one of the most essential components of living systems, robust analytical techniques available for phosphate sensing in natural waters and soils are essential for monitoring and predicting water quality and agronomic evaluation of phosphate. Using cyclic voltammetry, a point-of-use electrochemical sensor zirconium dioxide/zinc oxide/multiple-wall carbon nanotubes/ammonium molybdate tetrahydrate/screen printed electrode (ZrO 2 /ZnO/MWCNTs/AMT/SPE) was applied to explore the electro-redox reaction of phosphomolybdate complexes on the surface of electrode, which produced a quantitative electrochemical response of phosphate anions. The modification of the electrode surface with ZrO 2 /ZnO/MWCNTs nanocomposites is able to generate the electroactive species via chemical reaction between molybdenum (Mo(VI)) and the targeted phosphate anions, leading to a sensitive detection technique for trace phosphate with a lower detection limit (LOD = 2.0 × 10 -8 mol L -1 ), higher reproducibility, anti-interference, and precision in different soil sources. This system will be of great potential to advance the trace-level understanding of phosphate especially in field environmental analysis.

Aim: We aimed to develop and validate a comprehensive nomogram containing pre-treatment plasma HSP90AA1 to predict the risk of breast cancer onset and metastasis., Methods: We assessed the expression of HSP90s in breast cancer patients using an online database. To verify the results, 677 patients diagnosed with breast cancer and 146 patients with benign breast disease between 2014 and 2019 were selected from our hospital and were divided into cancer risk and metastasis risk cohorts. We focused on HSP90AA1 to elucidate the risks of onset and metastasis in the cohorts., Results: Expression levels of HSP90AA1 , HSP90AA2 , HSP90AB1 , HSP90B1 , and TRAP1 were linked to disease progression. Survival analysis using the GEPIA and OncoLnc databases indicated that the upregulation of HSP90AA1 and HSP90AB1 was related to poor overall survival. In the cancer risk cohort, carcinoembryonic antigen (CEA), carbohydrate antigen 153 (CA153), HSP90AA1, T cells%, natural killer cells%, B cells%, neutrophil count, monocyte count, and d-dimer were incorporated into the nomogram. A high Harrell's concordance index (C-index) value of 0.771 [95% confidence interval (CI), 0.725-0.817] could still be reached in the interval validation. In the metastasis risk cohort, predictors contained in the prediction nomogram included the use of CEA, CA153, HSP90AA1, carbohydrate antigen 125 (CA125), natural killer cells%, B cells%, platelet count, monocyte count, and d-dimer. The C-index was 0.844 (95% CI, 0.801-0.887) and it was well-calibrated. HSP90AA1 raised net clinical benefit of breast cancer onset and metastasis risk prediction nomogram in a range of risk thresholds (5-92%) and (1-90%)., Conclusion: Our study revealed that pretreatment plasma HSP90AA1 combined with other markers could conveniently predict the risk of breast cancer onset and metastasis., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2021 Liu, Zhang, Huang, Wei, Ning, Li, Liang, Liu and Zhang.)

Nano and colloidal particles (1-1000 nm) play important roles in phosphorus (P) migration and loss from agricultural soils; however, little is known about their relative distribution in arable crop soils under varying agricultural geolandscapes at the regional scale. Surface soils (0-20 cm depth) were collected from 15 agricultural fields, including two sites with different carbon input strategies, in Zhejiang Province, China, and water-dispersible nanocolloids (0.6-25 nm), fine colloids (25-160 nm), and medium colloids (160-500 nm) were separated and analyzed using the asymmetrical flow field flow fractionation technique. Three levels of fine-colloidal P content (3583-6142, 859-2612, and 514-653 μg kg -1 ) were identified at the regional scale. The nanocolloidal fraction correlated with organic carbon (C org ) and calcium (Ca), and the fine colloidal fraction with C org , silicon (Si), aluminum (Al), and iron (Fe). Significant linear relationships existed between colloidal P and C org , Si, Al, Fe, and Ca and for nanocolloidal P with Ca. The organic carbon controlled colloidal P saturation, which in turn affected the P carrier ability of colloids. Field-scale organic carbon inputs did not change the overall morphological trends in size fractions of water-dispersible colloids. However, they significantly affected the peak concentration in each of the nano-, fine-, and medium-colloidal P fractions. Application of chemical fertilizer with carbon-based solid manure and/or modified biochar reduced the soil nano-, fine-, and medium-colloidal P content by 30-40%; however,the application of chemical fertilizer with biogas slurry boosted colloidal P formation. This study provides a deep and novel understanding of the forms and composition of colloidal P in agricultural soils and highlights their spatial regulation by soil characteristics and carbon inputs.

Anthropogenic activities, such as mining, influence soil bacterial community composition and microbial distributions. In the current study, the patterns in microbial distribution and the environmental drivers shaping the soil bacterial community composition in the alpine mining area of the Tianshan Mountain region, China, were investigated, and the bacterial communities were analyzed using 16S rDNA pyrosequencing. The environmental factors and their relationships with the microbial community composition, structure, and diversity were also assessed. The soil organic carbon (SOC) concentration increased along the elevation gradient, with the highest concentration in the mining area, which increased microbial abundance and species richness. Some metals, like Ca, Cu, Pb, and Zn, accumulated significantly in the tailing area and were negatively correlated with the microbial community structure. Proteobacteria, Acidobacteria, Actinobacteria, and Verrucomicrobia were the dominant phyla; these dominant phyla were more abundant in the areas without mining than in the areas with mining at the same altitude. The relative abundance of Proteobacteria and Verrucomicrobia significantly increased along the elevation gradient, while that of Actinobacteria in the mining camp area was more than twice those in the other areas due to higher soil pH. Soil biomass was the highest in the valley. Collectively, these results elucidate the influence of anthropogenic mining activities on soil microbial communities in alpine mining soils and provide a basis for the future management of heavy metal-contaminated areas using the indigenous dominant bacterial phyla.

Objective: This paper summarizes the MRI imaging findings of primary central nervous system lymphoma (PCNSL) in the posterior cranial fossa to improve the accuracy of PCNSL diagnosis in the posterior cranial fossa., Methods: This study retrospectively analyzed the MRI imaging manifestations of 15 PCNSL posterior cranial fossa cases confirmed by puncture or surgical pathology from June 2017 to May 2018, including their occurrence sites, the number of lesions, MRI plain and enhanced manifestations, and diffusion-weighted imaging (DWI) and magnetic resonance spectroscopy. Imaging (MRS) performance., Results: A total of 15 cases were enrolled, including 10 cases of single lesion and five cases of multiple lesions. The total number of lesions was 25, which were in the cerebellar hemisphere and cerebellar vermis, midbrain, fourth ventricle, and pontine cerebellum. The lesions were round, irregular, nodular, patchy, with low or medium signals on T1WI, equal or slightly higher signals on T2WI, and enhanced with 25 meningiomas-like gray matter signals. All of them were significantly strengthened. "Acupoint sign" and "umbilical depression sign" were seen in eight lesions. There were 17 massive and nodular enhancements, four striped enhancements, three patchy enhancements, and one circular enhancement. five cases of DWI showed homogeneous high signal, two cases showed uneven high signal, and 3 cases showed medium signal. The ADC value of tumor parenchyma in 10 patients was (0.62±0.095)×10 -3 mm 2 /s. MRS examination showed obvious Lip peak in two cases., Conclusion: PCNSL in posterior cranial fossa has certain characteristics. DWI, ADC value and MRS are helpful to improve the correct diagnosis rate of PCNSL., (Copyright: © Pakistan Journal of Medical Sciences.)

Blending waste biomass for co-pyrolysis is generally regarded as a promising method for reduced-volume, value-added, and hazard-free treatment of sewage sludge. Hence, a comparison was made of the co-pyrolysis of sewage sludge with rice husk and with bamboo sawdust (1:1, w/w) at 400 and 700 °C and the properties and behaviors of selected metals in the corresponding biochars. Biochar produced by co-pyrolysis with both biomass wastes had larger (5 × 5 rectangle) aromatic clusters than did the sewage sludge biochar (4 × 4 rectangle) using the rectangle-like model on the basis of biochar molar H/C ratio, indicating increased aromaticity of the co-pyrolyzed biochars. Moreover, the molar O/C ratio of the sewage sludge-bamboo biochar was much lower than that of the sewage sludge-husk biochar, especially after pyrolysis at 700 °C (0.02 vs 0.27), suggesting greater recalcitrance to ageing. Co-pyrolysis of sewage sludge with husk invariably resulted in a higher percentage of metals studied in the residual fraction than co-pyrolysis with sawdust at the same temperature, leading to a lower risk index (14.2) because of the maximum metal encapsulation in the sewage sludge-husk biochar at 700 °C. Overall, co-pyrolysis of sewage sludge with husk provided higher metal immobilization but apparently lower biochar stability than co-pyrolysis with sawdust. These results provide an alternatively practical strategy for the safe disposal of sewage sludge and biomass wastes., (Copyright © 2020 Elsevier Inc. All rights reserved.)

Glyphosate, which has been widely reported to be a toxic pollutant, is often present at trace amounts in the environment. In this study, a novel copper-aluminum metal hydroxide doped graphene nanoprobe (labeled as CuAl-LDH/Gr NC) was first developed to construct a non-enzymatic electrochemical sensor for detection trace glyphosate. The characterization results showed that the synthesized CuAl-LDH had a high-crystallinity flowered structure, abundant metallic bands and an intercalated functional group. After mixed with Gr, the nanocomposites provided a larger surface area and better conductivity. The as-prepared CuAl-LDH/Gr NC dramatically improved the enrichment capability for glyphosate to realize the stripping voltammetry detection. The logarithmic linear detection range of the sensor was found to be 2.96 × 10 -9 -1.18 × 10 -6 mol L -1 with the detection limit of 1 × 10 -9 mol L -1 with excellent repeatability, good stability and anti-interference ability. Further, the sensor achieved satisfactory recovery rates in spiked surface water, ranging from 97.64% to 108.08%, demonstrating great accuracy and practicality.

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 + , Ca 2+ , and Mg 2+ . The optimum adsorbent dose and particle size were 4 g/L and 3-5 mm, respectively, for an aqueous solution containing 10 mg/L of ammonium under normal conditions (298 K and pH 7.0). Furthermore, the adsorption process was endothermic, following both the Langmuir (R 2  > 0.98) and Freundlich (R 2  > 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 20.8 mg/g (298 K 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 +  > Ca 2+  > Mg 2+ . Mechanisms for ammonium removal by FMML include diffusion, electrostatic attraction, oxidation, and complexation reaction., (© 2019 Water Environment Federation.)

Colloidal phosphorus (CP) as an additional route of P mobilization in soil solution has gained much attention. A batch experiment was conducted to investigate the effect of sheep manure-derived biochar (SMB) on CP release from various land uses (paddy, vegetable, tea, and citrus) at a rate of 0% as a control treatment (CK), 1% as a low (L) level, 2% as a middle (M) level, and 4% as a high (H) level of SMB application. The CP and MRP coll in the solution increased from 30.58 to 88.97% and from 2.45 to 55.54% of total P (TP), respectively. The SMB enhanced CP release in all the soils and all the treatments (except CK and L levels in tea soil; CK, L, and M levels in vegetable soil; and L and M levels in citrus soil). Multiple linear regression revealed a significant correlation between CP and MRP coll and between colloidal iron, aluminum, calcium, and total organic carbon (Fe coll , Al coll , Ca coll , and TOC coll ) and pH, which may play an important role as CP carriers that could depend on the pH. This study suggests that the application of SMB in the soil at an appropriate rate of 1 and 2% for tea and vegetable soils, respectively, could be beneficial to avoid the risk of CP release in water bodies.

Excessive application of phosphorus (P) fertilizer to the agriculture soil can lead to the P loss to the aquatic ecosystem. Three soils from different land use (tea, paddy, and vegetable soils) were treated with biogas slurry (BS) at rate of 79.8 kg ha -1 , anionic polyacrylamide (PAM) at rate of 12.5, 25 and 50 kg ha -1 , Gypsum (Gy) at rate of 5t ha -1 , and the control (Ck) without treatment, to control P losses in a laboratory batch experiment. The soil solution was analyzed for total P (TP), dissolved reactive P (DRP) and total dissolved P (TDP). Particulate P (PP) and dissolved unreactive P (DURP) were calculated by subtracting DRP from TP and TDP, respectively. The DRP was within a range of 68-98% of TP whereas PP varied in a range of 2-32% of TP and DURP was within a range of 0.1-19% of TP, depending on soil types and different treatments. The addition of PAM at a high rate and Gy together on the soil after BS application reduced the release of TP by 54, 46, and 51% and that of DRP by 61, 49, and 53% for tea, paddy and vegetable soils, respectively. However, the application of BS with PAM alone promoted the release of DRP by 77, 86, 70% for tea, paddy, and vegetable soils, respectively. This study suggests that the synergic application of PAM and Gy on soils after BS addition can be a good strategy to reduce P losses., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

The reuse of water in agriculture has become more common in water management worldwide. However, there is very limited information about nutrient retention in water reclamation management. In this study, an improved low impact development (LID) practice was constructed to investigate the synergistic effects of three substrates amendment on nitrogen (N) and phosphorus (P) retention under two irrigation modules: spray and drip irrigation. The orthogonal combination of the three substrates was controlled during four leaching events, with polyacrylamide (PAM), peat soil, and straw biochar application rates of 1, 2, and 4 g kg -1 ; 5, 10, and 20 g kg -1 ; and 10, 20, and 40 g kg -1 , respectively. Results showed that the optimum treatments for N and P were 2 g kg -1 of PAM; 2 g kg -1 of PAM, 10 g kg -1 of peat soil, and 40 g kg -1 of straw biochar, respectively. The highest amounts of N and P retention under spray and drip irrigation were 83.12 mg N kg -1 and 50.09 mg N·kg -1 , and 11.88 mg P·kg -1 and 7.47 mg P·kg -1 , respectively. The analysis of variance indicated that PAM, biochar, and peat soil affected the retention of leachate, N, and P differently. PAM application could not only improve the water, N, P retention capacity of soil, but also significantly increase the content of ＞2 mm water-stable soil aggregate (WSA) (p＜0.05), and there is an advisable linear relation between N, P retention and the content of ＞2 mm WSA (R 2  = 0.79, 0.67, respectively). Overall, this study concludes that a combined application of PAM and biochar could reduce P loss and increase the ＞2 mm WSA under leaching condition., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

The analytical techniques and instrumentation used to assess agricultural and rural nonpoint-source organic pollution loading are usually complex and expensive. There has been a strong demand for alternative methodologies to determine the presence and composition of organic pollutants and to predict their levels. In the current work, we investigated a simple and inexpensive approach combining excitation-emission matrix and support vector machine that measures pollution and predicts the levels of precursors to disinfection by-products, which are organic pollutants derived from agricultural and rural nonpoint sources in small watersheds. Through parallel factor analysis, a four-component model was developed to explain the composition of dissolved organic matter in water impacted by nonpoint-source pollution. Support vector classification and support vector regression with model components can use fluorescence properties as proxy indicators for nonpoint-source pollution. When the model components are used as input variables, formation potential of disinfection by-products can be predicted. This method provides water utilities managers with tools to control pollution, supervise aquatic environments, and ensure the safety of drinking water., (Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.)

Converting swine manure to biochar is an effective way to recycle valuable nutrients, but there are few reports on its feasibility as a phosphorus (P) source. The objective of this study was to clarify the unique nature, including P speciation, of manure biochar products under various pyrolysis temperatures. We used solution 31 P nuclear magnetic resonance and P K-edge X-ray adsorption near-edge spectroscopy (P XANES) to characterize P species in swine manure biochar. For every 100 °C increment starting from 300 °C, the P content in manure biochar increased by 2.16 to 3.37 g kg -1 . However, above 400 °C, organic P species did not appear anymore, and only inorganic P, including orthophosphate and pyrophosphate, existed. P K-edge XANES spectra further showed all biochar samples had higher percentages of Ca 3 (PO 4 ) 2 and NaP 2 O 7 , and lower percentages of FePO 4 , AlPO 4 , and inositol hexaphosphate compared to manure. Interestingly, percentages of Ca 3 (PO 4 ) 2 , FePO 4 , and AlPO 4 in MB400 (indicating manure pyrolysed at 400 °C) were comparable with those in MB700 while the percentage of NaP 2 O 7 was higher in MB400. Phosphorus release from MB400 maintained a relatively high level at 0.33 g kg -1 during the whole 300-h observation period. These results suggest that with a suitable pyrolysis temperature, it was feasible for manure biochar to be a P source alternative. Graphical abstract ᅟ.

Nonpoint sources are difficult to control because their nutrient contribution from different parts of a watershed can vary substantially. Identifying critical source areas of nutrient loss is an important step in watershed pollution mitigation programs. This study sought to use an integrated index model to differentiate between subbasins that serve as critical source areas of N and P nonpoint sources of pollution in China's Tiaoxi watershed. In contrast with previous N and P indices, multiple sources of pollution (i.e., agronomic activity, domestic wastewater, livestock farming, and aquaculture) were considered. Nitrogen and P source factors (i.e., N and P annual export loads) and transport factors were multiplied to determine the overall risk of nutrient loss in the integrated index model. Critical source areas were identified by a higher nutrient loss index. Of the 92 subbasins within the Tiaoxi watershed, 13 were determined to be critical sources for N, 10 for P, and seven for both N and P. Critical source area identification corresponds well with water quality data from the subbasins. The results show the potential use of the integrated index model for prioritizing and targeting watershed pollution mitigation activities at the subbasin level., (Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.)

Arsenic (As) and lead (Pb) commonly co-exist with high concentrations in paddy soil mainly due to human activities in south of China. This study investigates the effect of ferrous sulfate (FeSO 4 ) amendment and water management on rice growth and arsenic (As) and lead (Pb) accumulation in rice plants. A paddy soil co-contaminated with As and Pb was chosen for the pot experiment with three FeSO 4 levels (0, 0.25, and 1%, on a dry weight basis) and two water managements (flooded, non-flooded). The concentrations of As and Pb in iron plaques and rice plants were determined. Application of FeSO 4 and non-flooded conditions significantly accelerated the growth of rice plants. With the addition of FeSO 4 , iron plaques were significantly promoted and most of the As and Pb were sequestered in the iron plaques. The addition of 0.25% FeSO 4 and non-flooded conditions did not significantly change the accumulation of As and Pb in rice grains. The practice also significantly decreased the translocation factor (TF) of As and Pb from roots to above-ground parts which might have been aided by the reduction of As and Pb availability in soil, the preventing effect of rice roots, and the formation of more reduced glutathione (GSH). Flooded conditions decreased the Pb concentration in rice plants, but increased As accumulation. Moreover, rice grew thin and weak and even died under flooded conditions. Overall, an appropriate FeSO 4 dose and non-flooded conditions might be feasible for rice cultivation, especially addressing the As issue in the co-contaminated soil. However, further detailed studies to decrease the accumulation of Pb in edible parts and the field application in As and Pb co-contaminated soil are recommended.

Currently, environmental pollution by heavy metals is a global problem. Therefore, it is crucial to develop effective detection techniques to determine the levels of heavy metal contamination in various mediums. Voltammetry is a highly sensitive electrochemical method used for the in situ detection of heavy metal ions. This study investigates the current trends related to electrode modification, developments in materials, and optimization of the experimental parameters. We discuss the sensing performance of four kinds of nanomaterials capable of inorganic modification (metal nanoparticles, metal oxides, carbonaceous nanomaterials, and their nanocomposites). The impact of several important factors, such as the deposition potential and time, buffer solution types, and pH on the sensitivity, reproducibility, stability, and anti-interference ability of the detection process, especially with regard to the co-detection of several heavy metal ions, was reviewed. We noted that in addition to the application of voltammetry to water-related issues, it is suitable for rapid and simple identification and analyses of heavy metals in polluted soil and other mediums. Thus, it is important to conduct additional research on the application of voltammetry to this area., (Copyright © 2017 Elsevier B.V. All rights reserved.)

Aurora kinase A (AURKA) is a serine threonine kinase which affects chromosomal separation and mitotic spindle stability through interaction with the centrosome during mitosis. Two functional nonsynonymous polymorphisms of the AURKA gene (Ile31Phe and Val57Ile) have been reported recently. We analyzed the association between the two polymorphisms and risk of the occurrence of hepatitis B virus (HBV)-related hepatocellular carcinoma (HCC) in the Guangxi population consisting of 348 patients with HCC and 359 control subjects, and then validated the significant association in the Guangdong population consisting of 440 cases and 456 controls. All of the participants were of Chinese origin and HBV carriers. The two polymorphisms were genotyped by polymerase chain reaction-restriction fragment length polymorphism assay or Sequenom MassARRAY iPLEX platform. In the Guangxi population, carriers of the AURKA 31Phe allele (Ile/Phe + Phe/Phe) were significantly associated with decreased susceptibility to HBV-related HCC when compared with noncarriers (Ile/Ile) (odds ratio [OR] = 0.63, 95% confidence interval [CI] = 0.46-0.86, P = 3.4 × 10 -3 ). On the contrary, no significant association was found between Val57Ile and HBV-related HCC occurrence. The association of Ile31Phe with HBV-related HCC occurrence was confirmed in the Guangdong population (OR = 0.64, 95% CI = 0.49-0.83, P = 8.0 × 10 -4 ). The pooled analysis gave a joint P value of 5.5 × 10 -6 (joint OR = 0.63, 95% CI = 0.52-0.77). Our findings suggest that AURKA Ile31Phe may play a role in mediating the susceptibility to HBV-related HCC among Chinese., Competing Interests: CONFLICTS OF INTERESTS The authors have declared that no competing interests exist.

The effect of no-tillage (NT) on rice yield and nitrogen (N) behavior often varies considerably from individual studies. A meta-analysis was performed to assess quantitatively the effect of NT on rice yield and N uptake by rice, N use efficiency (NUE, i.e., fertilizer N recovery efficiency), and nutrient runoff losses. We obtained data from 74 rice-field experiments reported during the last three decades (1983-2013). Results showed the NT system brought a reduction of 3.8 % in the rice yield compared with conventional tillage (CT). Soil pH of 6.5-7.5 was favorable for the improvement of rice yield with the NT system, while a significant negative NT effect on rice yield was observed in sandy soils (p < 0.05). N rate, ranging from 120 to 180 kg N ha -1 , for at least 3 years was necessary for NT to enable rice yield comparable with that of CT. Furthermore, the observations indicated NT reduced N uptake and NUE of the rice by 5.4 and 16.9 %, while increased the N and P exports via runoff by 15.4 and 40.1 % compared with CT, respectively. Seedling cast transplantation, N rate within the range 120-180 kg N ha -1 , and employing NT for longer than 3 years should be encouraged to compromise between productivity and environmental effects of NT implementation in rice fields.

Nutrient runoff losses from cropping fields can lead to nonpoint source pollution; however, the level of nutrient export is difficult to evaluate, particularly at the regional scale. This study aimed to establish a novel yet simple approach for estimating total nitrogen (TN) and total phosphorus (TP) runoff losses from regional paddy fields. In this approach, temporal changes of nutrient concentrations in floodwater were coupled with runoff-processing functions in rice ( L.) fields to calculate nutrient runoff losses for three site-specific field experiments. Validation experiments verified the accuracy of this method. The geographic information system technique was used to upscale and visualize the TN and TP runoff losses from field to regional scales. The results indicated that nutrient runoff losses had significant spatio-temporal variation characteristics during rice seasons, which were positively related to fertilizer rate and precipitation. The average runoff losses over five study seasons were 20.21 kg N ha for TN and 0.76 kg P ha for TP. Scenario analysis showed that TN and TP losses dropped by 7.64 and 3.0%, respectively, for each 10% reduction of fertilizer input. For alternate wetting and drying water management, the corresponding reduction ratio was 24.7 and 14.0% respectively. Our results suggest that, although both water and fertilizer management can mitigate nutrient runoff losses, the former is significantly more effective., (Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.)

Nitrogen removal with different organic carbon effect was investigated using anaerobic baffled reactor (ABR) anammox reactor. Results indicated that organic carbon exert an important effect on nitrogen removal through anammox process. When the feeding COD concentration was lower than 99.7mgL(-1), nitrogen removal could be enhanced via the coexistence of denitrification and anammox. Elevated COD could further deteriorate the anammox activity with almost complete inhibition at the COD concentration of 284.1mgL(-1). The nitrogen removal contribution rate of anammox was varied from 92.7% to 6.9%. However, the anammox activity was recovered when the COD/TN was decreased from 2.33 to 1.25 with influent nitrite addition. And, the anammox process was again intensified from 27.0 to 51.2%. High-throughput Miseq sequencing analyses revealed that the predominant phylum changed from Chloroflexi to Proteobacteria with the elevated COD addition, which indicated COD concentration was the most important factor regulating the bacterial community structure., (Copyright © 2016 Elsevier Ltd. All rights reserved.)

Hepatitis B virus (HBV) infection is a common infectious disease. Here we perform a genome-wide association study (GWAS) among Chinese populations to identify novel genetic loci involved in persistent HBV infection. GWAS scan is performed in 1,251 persistently HBV infected subjects (PIs, cases) and 1,057 spontaneously recovered subjects (SRs, controls), followed by replications in four independent populations totally consisting of 3,905 PIs and 3,356 SRs. We identify a novel locus at 8p21.3 (index rs7000921, odds ratio=0.78, P=3.2 × 10(-12)). Furthermore, we identify significant expression quantitative trait locus associations for INTS10 gene at 8p21.3. We demonstrate that INST10 suppresses HBV replication via IRF3 in liver cells. In clinical plasma samples, we confirm that INST10 levels are significantly decreased in PIs compared with SRs, and negatively correlated with the HBV load. These findings highlight a novel antiviral gene INTS10 at 8p21.3 in the clearance of HBV infection.