Deciphering salt tolerance in tetraploid honeysuckle (Lonicera japonica Thunb.) from ion homeostasis, water balance and antioxidant defense.

Polyploid plants are usually salt tolerant, but the underlying mechanisms remain fragmental. This study aimed to dissect salt resistance of tetraploid honeysuckle (Lonicera japonica Thunb.) from ion balance, osmotic adjustment and antioxidant defense by contrasting with its autodiploid through pot experiments. Less salt-induced reduction in leaf and root biomass confirmed higher tolerance in tetraploid honeysuckle, and moreover, its greater stability of photosynthetic apparatus was verified by mild influence on delayed chlorophyll fluorescence transients. Compared with the diploid, greater root Na+ exclusion helped alleviate salt-induced decrease in leaf K+/Na+ for maintaining ion balance in tetraploid honeysuckle, and relied on Na+/H+ antiporter activity, because their difference of root Na+ exclusion disappeared after applying a specific inhibitor of Na+/H+ antiporter. Lower reduction in leaf relative water content suggested higher tolerance to osmotic pressure in tetraploid honeysuckle under salt stress, which hardly resulted from osmotic adjustment given the similar decrease extent of leaf osmotic potential with that in the diploid. In contrast to significant elevated leaf lipid peroxidation and superoxide dismutase and ascorbate peroxidase activities in the diploid, no obvious changes in them suggested that tetraploid honeysuckle never suffered salt-induced oxidative stress. According to more accumulated leaf chlorogenic acid and phenolics and greater elevated leaf phenylalanine ammonia-lyase activity and transcription, leaf phenolic synthesis was enhanced greater in tetraploid honeysuckle upon salt stress, which might serve to prevent oxidative threat by consuming reducing power. In conclusion, polyploidy enhanced salt tolerance in honeysuckle by maintaining ion homeostasis and water balance and preventing oxidative stress.

Partial substitution of chemical fertilizer by Trichoderma biofertilizer improved nitrogen use efficiency in wolfberry (Lycium chinense) in coastal saline land.

A two-year field trial was conducted to investigate the effects of partial substitution of chemical fertilizer (CF) by Trichoderma biofertilizer (TF) on nitrogen (N) use efficiency and associated mechanisms in wolfberry (Lycium chinense) in coastal saline land. As with plant biomass and fruit yield, apparent N use efficiency and plant N accumulation were also higher with TF plus 75% CF than 100% CF, indicating that TF substitution promoted plant growth and N uptake. As a reason, TF substitution stabilized soil N supply by mitigating steep deceases in soil NH4 +-N and NO3 -N concentrations in the second half of growing seasons. TF substitution also increased carbon (C) fixation according to higher photosynthetic rate (Pn) and stable 13C abundance with TF plus 75% CF than 100% CF. Importantly, leaf N accumulation significantly and positively related with Pn, biomass, and fruit yield, and structural equation modeling also confirmed the importance of the causal relation of N accumulation coupled with C fixation for biomass and yield formation. Consequently, physiological and agronomical N use efficiencies were significantly higher with TF plus 75% CF than 100% CF. Overall, partial substitution of CF by TF improved N use efficiency in wolfberry in coastal saline land by stabilizing soil N supply and coupling N accumulation with C fixation.

Self-luminescent europium based metal organic frameworks nanorods as a novel electrochemiluminescence chromophore for sensitive ulinastatin detection in biological samples.

In this work, we developed a novel electrochemiluminescence (ECL) biosensor for ulinastatin (UTI) detection based on self-luminescent metal-organic framework (L-MOF) nanomaterials. The L-MOFs could be simply prepared by one-pot methods using Eu3+ and 4,4',4″-s-triazine-1,3,5-triyltri-m-aminobenzoic acid (H3TATAB) as the metallic center and organic ligand, respectively. The Eu-TATAB exhibited high efficiency and stable ECL performance when using K2S2O8 as coreactant. For the established biosensor, Eu-TATAB was both used as the ECL chromophore and protein carrier due to its outstanding biocompatibility and large superficial area, which could load sufficient antibodies to link with antigen in the biosensor for subsequent detection. The established sandwich ECL biosensor showed a wide linear range of 0.1 ng mL-1 - 105 ng mL-1 and a low limit of detection of 9.7 pg mL-1 for UTI detection. In addition, the developed ECL biosensor could also be successfully applied to the real UTI sample determination in serum. The reported biosensor strategy could provide a guide for developing more other novel and promising high-performance ECL nanomaterials, and also be used as a potential method for ultrasensitive UTI detection in disease research.

Highly Efficient Silver Catalyst Supported by a Spherical Covalent Organic Framework for the Continuous Reduction of 4-Nitrophenol.

Developing new materials and novel technologies for the highly efficient treatment of toxic organic pollutants is highly desirable. Chemical reduction based on heterogeneous substrate/noble metal catalysts and the reducing agent NaBH4 has become an effective method in recent years. Here, a spherical covalent organic framework (SCOF) was designed to provide basic sites for Ag ions, by which small Ag NPs were immobilized on the SCOF to form Ag NPs@SCOF microspheres. The prepared microspheres exhibited a high catalytic reduction ability toward 4-nitrophenol (4-NP). An optimized permeation flux of 2000 L m-2 h-1 (LMH) and a more than 99% 4-NP reduction efficiency were obtained with flow-through experiments, which are far better than the reported results (below 200 LMH). Moreover, the microspheres could maintain stable catalytic performance under a continuous flow-through process. Our work provides an efficient material and technology that can be applied to easily treat toxic organic pollutants.

An Electrochemical Sensor Based on Gold and Bismuth Bimetallic Nanoparticles Decorated L-Cysteine Functionalized Graphene Oxide Nanocomposites for Sensitive Detection of Iron Ions in Water Samples.

In this work, gold and bismuth bimetallic nanoparticles decorated L-cysteine functionalized graphene oxide nanocomposites (Au-BiNPs/SH-GO) were prepared and applied to selective detection of Fe(III) in lake and seawater samples by modifying onto glassy carbon electrodes. Bimetallic nanoparticles have various excellent properties and better catalytic properties because of the unique synergistic effect between metals. The modified electrode was characterized by scanning electron microscopy, energy dispersive X-ray spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, and Raman spectroscopy. Under optimized conditions, current peak intensity increased linearly with increasing Fe(III) concentration over the range of 0.2-50 µM and a detection limit of 0.07 µM (S/N = 3). The Au-BiNPs/SH-GO/GCE was used for the determination of Fe(III) in lake and seawater samples with recoveries ranged from 90 to 103%. Those satisfactory results revealed the potential application of the Au-BiNPs/SH-GO electrochemical sensor for heavy metals detection in environmental monitoring.

Hybrid permeable metal-base transistor with large common-emitter current gain and low operational voltage.

We demonstrate the suitability of N,N'-diphenyl-N,N'-bis(1-naphthylphenyl)-1,1'-biphenyl-4,4'-diamine (NPB), an organic semiconductor widely used in organic light-emitting diodes (OLEDs), for high-gain, low operational voltage nanostructured vertical-architecture transistors, which operate as permeable-base transistors. By introducing vanadium oxide (V2O5) between the injecting metal and NPB layer at the transistor emitter, we reduced the emitter operational voltage. The addition of two Ca layers, leading to a Ca/Ag/Ca base, allowed to obtain a large value of common-emitter current gain, but still retaining the permeable-base transistor character. This kind of vertical devices produced by simple technologies offer attractive new possibilities due to the large variety of available molecular semiconductors, opening the possibility of incorporating new functionalities in silicon-based devices.

Improved potentiometric response of all-solid-state Pb(2+)-selective electrode.

Zero-current ion-flux has a great influence on the characteristics of the ion-selective electrodes. In this work the improvement of analytical performance of all-solid-state Pb(2+)-selective membrane electrodes was demonstrated by adjusting the transmembrane ion flux. The study is focused on the relationship between the conditioning solution and the linear working range of the obtained electrodes for different sample matrixes. Results show that the electrode with appropriate conditioning keeps good reproducibility within linear working range. The utility of the electrode has been tested by successfully determining Pb(2+) concentration in real water samples.

A solid-contact Pb(2+)-selective electrode using poly(2-methoxy-5-(2'-ethylhexyloxy)-p-phenylene vinylene) as ion-to-electron transducer.

In this work, a novel all-solid-state polymeric membrane Pb(2+)-selective electrode was developed by using for the first time poly(2-methoxy-5-(2'-ethylhexyloxy)-p-phenylene vinylene) (MEH-PPV) as solid contact. To demonstrate the ion-to-electron transducing ability of MEH-PPV, chronopotentiometry and electrochemical impedance spectroscopy measurements were carried out. The proposed electrodes showed a Nernstian response of 29.1 mV decade(-1) and a lower detection limit of subnanomolar level. No water film was observed with the conventional plasticized PVC membrane. This work demonstrates a new strategy for the fabrication of robust potentiometric ion sensors.

Synthesis and characterization of monoazathiacrown ethers as ionophores for polymeric membrane silver-selective electrodes.

Nine monoazathiacrown ethers have been synthesized and explored as ionophores for polymeric membrane Ag(+)-selective electrodes. Potentiometric responses reveal that the ion-selective electrodes (ISEs) based on 2,2'-thiodiethanethiol derivatives can exhibit excellent selectivities toward Ag(+). The plasticized poly(vinyl chloride) membrane electrode using 22-membered N(2)S(5)-ligand as ionophore has been characterized and its logarithmic selectivity coefficients for Ag(+) over most of the interfering cations have been determined as <-8.0. Under optimal conditions, a lower detection limit of 2.2x10(-10)M can be obtained for the membrane Ag(+)-ISE.