Microplastics are emerging pollutants that have recently aroused considerable concern but most toxicological studies have focused on marine biota, with little investigation of the influence of ...microplastics on terrestrial ecosystems. Here, we fed the soil oligochaete Enchytraeus crypticus with oatmeal containing 0, 0.025, 0.5, and 10% (dry weight basis) nano-polystyrene (0.05–0.1 μm particle size) to elucidate the impact of microplastics on the growth and gut microbiome of Enchytraeus crypticus. We observed a significant reduction of weight in the animals fed 10% polystyrene and an increase in the reproduction of those fed 0.025%. More importantly, using 16S rRNA amplification and high-throughput sequencing we found a significant shift in the microbiome of those fed 10% microplastics with significant decreases in the relative abundance of the families Rhizobiaceae, Xanthobacteraceae and Isosphaeraceae. These families contain key microbes that contribute to nitrogen cycling and organic matter decomposition.
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•Exposure to nano-polystyrene disrupted the Enchytraeus crypticus microbiome.•Nano-polystyrene led to a decrease in bacterial diversity and a structural shift.•Exposure to nano-polystyrene altered the weight and reproduction of E. crypticus.
Nano-polystyrene exposure disrupted the microbiome of Enchytraeus crypticus, leading to a decrease in microbial diversity and a structural shift in bacterial composition.
Aims. The nonthermal radiative properties of 18 pulsar wind nebulae (PWNe) are studied in the 1D leptonic model. Methods. The dynamical and radiative evolution of a PWN in a nonradiative supernova ...remnant are self-consistently investigated in this model. The leptons (electrons/positrons) are injected with a broken power-law form, and nonthermal emission from a PWN is mainly produced by time-dependent relativistic leptons through synchrotron radiation and inverse Compton process. Results. Observed spectral energy distributions (SEDs) of all 18 PWNe are reproduced well, where the indexes of low-energy electron components lie in the range of 1.0–1.8 and those of high-energy electron components in the range of 2.1–3.1. Our results show that FX/Fγ > 10 for young PWNe; 1 <FX/Fγ ≤ 10 for evolved PWNe, except for G292.0+1.8; and FX/Fγ ≤ 1 for mature/old PWNe, except for CTA 1. Moreover, most PWNe are particle-dominated. Statistical analysis for the sample of 14 PWNe further indicate that (1) not all pulsar parameters have correlations with electron injection parameters, but electron maximum energy and PWN magnetic field correlate with the magnetic field at the light cylinder, the potential difference at the polar cap, and the spin-down power; (2) the spin-down power positively correlates with radio, X-ray, bolometric, and synchrotron luminosities, but does not correlate with gamma-ray luminosity; (3) the spin-down power positively correlates with radio, X-ray, and γ-band surface brightness; and (4) the PWN radius and the PWN age negatively correlate with X-ray luminosity, the ratio of X-ray to gamma-ray luminosities, and the synchrotron luminosity.
The development of chemically recyclable polymers offers a solution to the end-of-use issue of polymeric materials and provides a closed-loop approach toward a circular materials economy. However, ...polymers that can be easily and selectively depolymerized back to monomers typically require low-temperature polymerization methods and also lack physical properties and mechanical strengths required for practical uses. We introduce a polymer system based on γ-butyrolactone (GBL) with a trans-ring fusion at the α and β positions. Such trans-ring fusion renders the commonly considered as nonpolymerizable GBL ring readily polymerizable at room temperature under solvent-free conditions to yield a high-molecular weight polymer. The polymer has enhanced thermostability and can be repeatedly and quantitatively recycled back to its monomer by thermolysis or chemolysis. Mixing of the two enantiomers of the polymer generates a highly crystalline supramolecular stereocomplex.
Purpose
Demonstrate a novel fast method for reconstruction of multi‐dimensional MR fingerprinting (MRF) data using deep learning methods.
Methods
A neural network (NN) is defined using the TensorFlow ...framework and trained on simulated MRF data computed with the extended phase graph formalism. The NN reconstruction accuracy for noiseless and noisy data is compared to conventional MRF template matching as a function of training data size and is quantified in simulated numerical brain phantom data and International Society for Magnetic Resonance in Medicine/National Institute of Standards and Technology phantom data measured on 1.5T and 3T scanners with an optimized MRF EPI and MRF fast imaging with steady state precession (FISP) sequences with spiral readout. The utility of the method is demonstrated in a healthy subject in vivo at 1.5T.
Results
Network training required 10 to 74 minutes; once trained, data reconstruction required approximately 10 ms for the MRF EPI and 76 ms for the MRF FISP sequence. Reconstruction of simulated, noiseless brain data using the NN resulted in a RMS error (RMSE) of 2.6 ms for T1 and 1.9 ms for T2. The reconstruction error in the presence of noise was less than 10% for both T1 and T2 for SNR greater than 25 dB. Phantom measurements yielded good agreement (R2 = 0.99/0.99 for MRF EPI T1/T2 and 0.94/0.98 for MRF FISP T1/T2) between the T1 and T2 estimated by the NN and reference values from the International Society for Magnetic Resonance in Medicine/National Institute of Standards and Technology phantom.
Conclusion
Reconstruction of MRF data with a NN is accurate, 300‐ to 5000‐fold faster, and more robust to noise and dictionary undersampling than conventional MRF dictionary‐matching.
The development of chemically recyclable polymers promises a closed‐loop approach towards a circular plastic economy but still faces challenges in structure/property diversity and depolymerization ...selectivity. Here we report the first successful coordination ring‐opening polymerization of 4,5‐trans‐cyclohexyl‐fused γ‐butyrolactone (M1) with lanthanide catalysts at room temperature, producing P(M1) with Mn up to 89 kg mol−1, high thermal stability, and a linear or cyclic topology. The same catalyst also catalyses selective depolymerization of P(M1) back to M1 exclusively at 120 °C. This coordination polymerization is also living, enabling the synthesis of well‐defined block copolymer.
Living and reborn: Metal‐mediated coordination polymerization of a trans‐fused six‐five bicyclic lactone is living or catalytic, creating linear or cyclic polymers with high thermal stability and complete chemical recyclability.
Integrating thermodynamically favorable ethanol reforming reactions with hybrid water electrolysis will allow room‐temperature production of high‐value organic products and decoupled hydrogen ...evolution. However, electrochemical reforming of ethanol has not received adequate attention due to its low catalytic efficiency and poor selectivity, which are caused by the multiple groups and chemical bonds of ethanol. In addition to the thermodynamic properties affected by the electronic structure of the catalyst, the dynamics of molecule/ion dynamics in electrolytes also play a significant role in the efficiency of a catalyst. The relatively large size and viscosity of the ethanol molecule necessitates large channels for molecule/ion transport through catalysts. Perforated CoNi hydroxide nanosheets are proposed as a model catalyst to synergistically regulate the dynamics of molecules and electronic structures. Molecular dynamics simulations directly reveal that these nanosheets can act as a “dam” to enrich ethanol molecules and facilitate permeation through the nanopores. Additionally, the charge transfer behavior of heteroatoms modifies the local charge density to promote molecular chemisorption. As expected, the perforated nanosheets exhibit a small potential (1.39 V) and high Faradaic efficiency for the conversion of ethanol into acetic acid. Moreover, the concept in this work provides new perspectives for exploring other molecular catalysts.
Nanoporous ultrathin bimetallic compound sheets are used as a model catalyst to realize synergistic optimization of ethanol molecular spatial distribution and chemisorption. They exhibit a small potential (1.39 V) and high Faradaic efficiency for acetic acid.
G‐quadruplex DNA show structural polymorphism, leading to challenges in the use of selective recognition probes for the accurate detection of G‐quadruplexes in vivo. Herein, we present a tripodal ...cationic fluorescent probe, NBTE, which showed distinguishable fluorescence lifetime responses between G‐quadruplexes and other DNA topologies, and fluorescence quantum yield (Φf) enhancement upon G‐quadruplex binding. We determined two NBTE‐G‐quadruplex complex structures with high Φf values by NMR spectroscopy. The structures indicated NBTE interacted with G‐quadruplexes using three arms through π–π stacking, differing from that with duplex DNA using two arms, which rationalized the higher Φf values and lifetime response of NBTE upon G‐quadruplex binding. Based on photon counts of FLIM, we detected the percentage of G‐quadruplex DNA in live cells with NBTE and found G‐quadruplex DNA content in cancer cells is 4‐fold that in normal cells, suggesting the potential applications of this probe in cancer cell detection.
G4 imaging: A tripodal cationic fluorescence probe, NBTE, was used for the visualization (based on fluorescence lifetime) and quantification (based on photon counts) of G‐quadruplex DNA in live cells by fluorescence lifetime imaging microscopy (FLIM). Structural studies provided a structural basis for the DNA‐topology‐based fluorescence response of NBTE.
Animal manure application as organic fertilizer does not only sustain agricultural productivity and increase soil organic carbon (SOC) stocks, but also affects soil nitrogen cycling and nitrous oxide ...(N2O) emissions. However, given that the sign and magnitude of manure effects on soil N2O emissions is uncertain, the net climatic impact of manure application in arable land is unknown. Here, we performed a global meta‐analysis using field experimental data published in peer‐reviewed journals prior to December 2015. In this meta‐analysis, we quantified the responses of N2O emissions to manure application relative to synthetic N fertilizer application from individual studies and analyzed manure characteristics, experimental duration, climate, and soil properties as explanatory factors. Manure application significantly increased N2O emissions by an average 32.7% (95% confidence interval: 5.1–58.2%) compared to application of synthetic N fertilizer alone. The significant stimulation of N2O emissions occurred following cattle and poultry manure applications, subsurface manure application, and raw manure application. Furthermore, the significant stimulatory effects on N2O emissions were also observed for warm temperate climate, acid soils (pH < 6.5), and soil texture classes of sandy loam and clay loam. Average direct N2O emission factors (EFs) of 1.87% and 0.24% were estimated for upland soils and rice paddy soils receiving manure application, respectively. Although manure application increased SOC stocks, our study suggested that the benefit of increasing SOC stocks as GHG sinks could be largely offset by stimulation of soil N2O emissions and aggravated by CH4 emissions if, particularly for rice paddy soils, the stimulation of CH4 emissions by manure application was taken into account.
The uncertain manure effects on N2O emissions constrain evaluation of the net climatic impact of manure application in arable lands. A global meta‐analysis was performed to quantify the overall responses of N2O emissions to manure application relative to synthetic N fertilizer in agricultural soils. Manure application on average significantly increased N2O emissions by 32.7% as compared to synthetic N fertilizer alone, and the sign and magnitude of N2O emissions were dependent on manure characteristics, climate, and soil properties. The benefit of C sequestration could be largely offset by stimulation of soil N2O emissions and aggravated by CH4 emissions if, particularly for rice paddy soils, the stimulation of CH4 emissions by manure application was taken into account.
Superelastic carbon aerogels have been widely explored by graphitic carbons and soft carbons. These soft aerogels usually have delicate microstructures with good fatigue resistance but ultralow ...strength. Hard carbon aerogels show great advantages in mechanical strength and structural stability due to the sp3‐C‐induced turbostratic “house‐of‐cards” structure. However, it is still a challenge to fabricate superelastic hard carbon‐based aerogels. Through rational nanofibrous structural design, the traditional rigid phenolic resin can be converted into superelastic hard carbon aerogels. The hard carbon nanofibers and abundant welded junctions endow the hard carbon aerogels with robust and stable mechanical performance, including superelasticity, high strength, extremely fast recovery speed (860 mm s−1), low energy‐loss coefficient (<0.16), long cycle lifespan, and heat/cold‐endurance. These emerging hard carbon nanofiber aerogels hold a great promise in the application of piezoresistive stress sensors with high stability and wide detection range (50 kPa), as well as stretchable or bendable conductors.
A family of hard carbon aerogels with nanofibrous structure templated by various nanofibers is fabricated, displaying robust and stable mechanical performances, including high strength, extremely fast recovery speed (860 mm s−1), and ultralow energy loss coefficient (<0.16). After being compressed for 104 cycles (50% strain), they show only ≈2% plastic deformation and retain ≈93% stress.
Construction of robust, stereocomplexed (sc) crystalline material, based on a recently discovered infinitely recyclable polymer system, requires blending of enantiomeric polymer chains produced from ...respective enantiopure, fused six‐five bicyclic lactones. Herein, the stereoselective polymerization of the racemic monomer by yttrium catalysts bearing tetradentate ligands is reported, where the tethered donor sidearm switches the heteroselectivity of the catalyst to isoselectivity when it is changed from the β‐OMe to β‐NMe2 sidearm. The latter catalyst produces an isotactic stereoblock polymer (Pm up to 0.95) that forms the crystalline sc‐material with a Tm of up to 171 °C. This sc‐material can be fully depolymerized back to rac‐monomer in a quantitative yield and purity, thus establishing its circular life cycle.
The circle of life: The stereoselective polymerization of the racemic monomer by yttrium catalysts bearing tetradentate ligands is reported, where the tethered donor sidearm switches the heteroselectivity of the catalyst to isoselectivity when it is changed from the β‐OMe to β‐NMe2 sidearm. The latter produces an isotactic stereoblock polymer that forms the crystalline stereocomplexed material, which can be fully depolymerized.
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