JOURNAL OF PLANT GROWTH REGULATION
·
2017
·Vol. 37
·期 3
·745-754
·
IF 2.073
Zhang Qi,Li Li,Li Jiayu,Wang Haibin,Fang Changxun,Yang Xiaoyan,He Haibin
An allelopathic rice PI312777 and a non-allelopathic rice Lemont were hydroponically cultured and treated with extracts of seeds and tissues and root exudates of barnyard grass ( Echinochloa crus-galli , BYG) to induce an allelopathic response. The results of bioassays showed that the % inhibition of two rice leaf extracts was significantly ( p < 0.05) increased by treatment with BYG root exudates. This induced trait was dosage- and time-dependent. The highest % inhibition for both PI312777 and Lemont was obtained following treatment with 15 mL of BYG root exudates for 2 days. Under these conditions, total allelopathy (TA) values of PI312777 on root length, plant height, and plant dry weight of BYG were 73.39, 68.01, and 70.42%, respectively, and induced allelopathy (IA) values were 21.53, 17.04, and 16.62%, respectively, accounting for 24–29% of TA. Correspondingly, TA values of Lemont were 28.38, 21.38, and 23.38%, respectively, and IA values were 14.49, 11.37, and 12.11%, respectively, accounting for 51–53% of TA. The % inhibition of two rice culture solutions was in agreement with the results of their leaf extracts. The total contents of 7 phenolic acids in the culture solutions of PI312777 and Lemont were 2.18 and 1.47 times, respectively, as much as those in the control solutions. The phenylalanine ammonia-lyase ( PAL ) gene in PI312777 leaves was significantly up-regulated after induction treatments. The results indicated that rice allelopathy is a chemical induction mechanism, and confirmed that chemical induction to raise rice allelopathy is a practical and feasible method.
研究领域:
植物学
·
农业科学
·
分子生物学
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产品关联
DOI
高影响因子
eLife
·
2020
·
IF 7.08
Xiaoyun Hu,Shuangli Su,Qingsong Liu,Yaoyu Jiao,Yufa Peng,Yunhe Li,Ted CJ Turlings
Plants typically release large quantities of volatiles in response to herbivory by insects. This benefits the plants by, for instance, attracting the natural enemies of the herbivores. We show that the brown planthopper (BPH) has cleverly turned this around by exploiting herbivore-induced plant volatiles (HIPVs) that provide safe havens for its offspring. BPH females preferentially oviposit on rice plants already infested by the rice striped stem borer (SSB), which are avoided by the egg parasitoid Anagrus nilaparvatae, the most important natural enemy of BPH. Using synthetic versions of volatiles identified from plants infested by BPH and/or SSB, we demonstrate the role of HIPVs in these interactions. Moreover, greenhouse and field cage experiments confirm the adaptiveness of the BPH oviposition strategy, resulting in 80% lower parasitism rates of its eggs. Besides revealing a novel exploitation of HIPVs, these findings may lead to novel control strategies against an exceedingly important rice pest.
研究领域:
生态学
·
昆虫学
·
植物保护
✓ 已验证
DOI
高影响因子
JOURNAL OF PEST SCIENCE
·
2024
·
IF 4.3
Liu Yu-Xiao,Han Wen-Hao,Wang Jun-Xia,Zhang Feng-Bin,Ji Shun-Xia,Zhong Yu-Wei,Liu Shu-Sheng,Wang Xiao-Wei
Plants face an array of insect herbivores and have evolved complex defense approaches against various insect feeding strategies. However, little is known about how plants respond to successive attacks by herbivores with different feeding modes and coordinate their diverse defense mechanisms. In this study, we unveil that inducible jasmonic acid (JA) accumulation in response to leaf-chewing insects augments plant resistance and repellence to sequential leaf-chewing insect (caterpillar) and phloem-feeding insect (whitefly) infestations. Conversely, constitutive and whitefly inducible salicylic acid (SA) accumulation exclusively bolsters defense against later-stage whitefly invasion. Through assessments of herbivore performance and preferences on wild-type, JA-deficient, and SA-deficient plants, we show that JA/SA levels regulate plant resistance to both initial and sequential herbivores. Notably, JA or SA accumulation due to caterpillar or whitefly attacks does not substantially affect constitutive levels of the other compound, despite their antagonistic crosstalk. Furthermore, exogenous JA application in tobacco elicits efficient defense against successive caterpillar and whitefly assaults, surpassing SA's efficacy, albeit with associated growth penalties. Our discoveries demonstrate that plants can tailor their defense strategies against initial and sequential insects with different feeding modes. This customized defense is facilitated by JA/SA responses and their intricate cross-talk while taking account of the growth-defense trade-off.
研究领域:
植物学
·
生态学
✓ 已验证
产品关联
DOI
高影响因子
FUEL
·
2022
·
IF 8.035
Yi Liu,Ying Chen,Shuang Ma,Xianlong Liu,Xiangwen Zhang,Ji-Jun Zou,Lun Pan
High-energy–density (HED) fuels have attracted extensive attention for volume-fixed aerospace vehicles because they can provide more propulsion energy to increase the payload and range of aerospace vehicles. Herein, we report a route for synthesis of HED fuel, pentacyclo[8.2.1.1 4,7 .0 2,9 .0 3,8 ]tetradecane (PCTD) with strained structure, by photoinduced intermolecular [2 + 2] cycloaddition of norbornene (NBE). The triplet quenching and phosphorescence quenching results indicate that NBE cycloaddition is conducted through the photosensitized processes containing triplet–triplet energy transfer, cyclization and relaxation. The reaction conditions are optimized to obtain the high photocatalytic activity, with the NBE conversion and PCTD selectivity reaching 78.7% and 94.4%, respectively. Moreover, a kinetic model is proposed with the reaction rate equation being correlated with the incident light flux, with the pseudo reaction kinetics parameters and reaction rate equations obtained. Importantly, PCTD shows high density of 1.024 g/mL and high volumetric net heat of combustion of 42.98 MJ/L, much higher than those of JP-10. In addition, blending with JP-10 or QC can significantly improve cryogenic properties of blended fuels, which is very promising for the practical application.
研究领域:
化学工程
·
能源科学
✓ 已验证
产品关联
DOI
高影响因子
CHINESE JOURNAL OF CHEMICAL ENGINEERING
·
2023
·
IF 3.8
Jinxiu Hu,Xianlong Liu,Yi Liu,Kang Xue,Chengxiang Shi,Xiangwen Zhang,Li Wang,Ji-Jun Zou,Lun Pan
High-energy-density fuels are important for volume-limited aerospace vehicles, but the increase of the fuel energy density always leads to poor cryogenic performance. Herein, we investigated the transposed Paternò-Büchi reaction of biomass cyclic ketone and cyclic alkene to synthesize the new kind of alkyl-substituted polycyclic hydrocarbon fuels with high energy density and good cryogenic performance. The triplet-energy-quenching results and phosphorescent emission spectra reveal the sensitization mechanism of the reaction, including photosensitizer excitation, triplet-triplet energy transfer, cyclization and relaxation, and the possible reaction path was revealed by the DFT calculations. The reaction conditions of photosensitizer type and addition, molar ratio of substrates, reaction temperature and incident light intensity were optimized, with the target product yield achieving 65.5%. Moreover, the reaction dynamics of the reaction rate versus the light intensity is established. After hydrogenation deoxygenation reaction, three fuels with high density of 0.864-0.938 g·ml −1 and low freezing point of <−55 °C are obtained. This work provides a benign and effective approach to synthesize high-performance fuels.
研究领域:
化学工程
·
能源科学
·
合成化学
✓ 已验证
产品关联
DOI
高影响因子
ACS Applied Materials & Interfaces
·
2024
·
IF 8.3
Xiaohui Liu,Chudong Chen,Yonghong Xiao,Xianli Li,Ke Xu,Xin Lian,Jin Z. Zhang,Binbin Luo
In this work, two zero-dimensional (0D) metal halide hybrids L2ZnBr4 [1, L = (E)-4-(2-(1H-pyrrol-3-yl)vinyl)-1-methylpyridin-1-ium] and L6Pb3Br12 (2) were prepared, which demonstrated photochromism and photoinduced cracking. Upon irradiation at 450 nm, a single crystal-to-single crystal transformation occurred as a result of the [2 + 2] photocycloaddition of L. Interestingly, compared to the complete photocycloaddition of L in 1, only two-thirds of L monomers could be photodimerized in 2 because of the difference in L orientation. 1 shows reversible photochromic behavior including rapid response time, few cracks, high conversion rate, and good reaction reversibility, while 2 exhibits no significant color change but distinct photoinduced cracking because of the large local lattice strain induced by inhomogeneous and anisotropic deformation. Moreover, the photocycloaddition of L results in the distinct shift of photoluminescence of 1 and 2, attributed to the variation in conjugation of π electrons and distortion of metal halide clusters. As a proof-of-concept, reversible optical writing is demonstrated for 1. These findings provide new insights into the design of stimuli-responsive multifunctional materials.
研究领域:
材料科学
·
化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
BIOMACROMOLECULES
·
2017
·
IF 5.246
Wen-Jian Zhang,Chun-Yan Hong,Cai-Yuan Pan
An ingenious formulation of RAFT dispersion polymerization based on photosensitive monomers of 2-nitrobenzyl methacrylate (NBMA) and 7-(2-methacryloyloxy-ethoxy)-4-methyl-coumarin (CMA) is reported herein. Various morphologies, such as spherical micelle, nanoworm, lamella, and vesicle, are fabricated at up to 20% solids content. Photoinduced cleavage of the NBMA moieties and dimerization of the coumarin moieties are simultaneously triggered upon UV (365 nm) irradiation. The former endows the cores of the nano-objects with abundant carboxyl groups, resulting in the transformation of the hydrophobic cores to hydrophilic ones. The latter induces the core-cross-linking of the nano-objects, which endows the nano-objects with enhanced structural stability and prevents the nanoparticle-to-unimer disassembly. The resultant nano-objects exhibit superior structural stability and excellent performances for drug delivery, including high drug loadings, pH-stimuli release, and high-efficient endosomal escape.
研究领域:
材料科学
·
药学
·
生物医学工程
✓ 已验证
产品关联
DOI
PubMed
高影响因子
ENVIRONMENTAL SCIENCE & TECHNOLOGY
·
2021
·
IF 9.028
Jingyi Lin,Qin Dai,He Zhao,Hongbin Cao,Tianyu Wang,Guangwei Wang,Chuncheng Chen
Photoinduced interfacial release of volatile organic compounds (VOCs) from surfactants receives emerging concerns. Here, we investigate the photoreaction of 1-nonanol (NOL) as a model surfactant at the air–water interface, especially for the important role of 1O2 in the formation of VOCs. The production of VOCs is real-time quantitated. The results indicate that the oxygen content apparently affects the total yields of VOCs during the photoreaction of interfacial NOL. The photoactivity of NOL is about 8 times higher under air than that under nitrogen, which is mainly attributed to the generation of 1O2. Additionally, the production of VOCs increased by about 4 times with the existence of the air–water interface. Quenching experiments of 1O2 also illustrate the contribution of 1O2 to VOC formation, which could reach more than 95% during photoirradiation of NOL. Furthermore, density functional theory calculations show that 1O2 generated via energy transfer of photosensitizers can abstract two hydrogen atoms from a fatty alcohol molecule. The energy barrier of this reaction is 72.3 kJ/mol, and its reaction rate coefficient is about 2.742 s–1 M–1. 1O2 significantly promotes photoinduced oxidation of fatty alcohols and VOC formation through hydrogen abstraction, which provides a new insight into the interfacial photoreaction.
研究领域:
环境科学
·
物理化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Journal of the American Chemical Society
·
2024
·
IF 14.4
Kai-Yuan Huang,Zhi-Qiang Yang,Ming-Rui Yang,Tian-Shui Chen,Shurong Tang,Wei-Ming Sun,Qiaofeng Yao,Hao-Hua Deng,Wei Chen,Jianping Xie
Metal nanoclusters (MNCs) represent a promising class of materials for catalytic carbon dioxide and proton reduction as well as dihydrogen oxidation. In such reactions, multiple proton-coupled electron transfer (PCET) processes are typically involved, and the current understanding of PCET mechanisms in MNCs has primarily focused on the sequential transfer mode. However, a concerted transfer pathway, i.e., concerted electron–proton transfer (CEPT), despite its potential for a higher catalytic rate and lower reaction barrier, still lacks comprehensive elucidation. Herein, we introduce an experimental paradigm to test the feasibility of the CEPT process in MNCs, by employing Au18(SR)14 (SR denotes thiolate ligand), Au22(SR)18, and Au25(SR)18– as model clusters. Detailed investigations indicate that the photoinduced PCET reactions in the designed system proceed via an CEPT pathway. Furthermore, the rate constants of gold nanoclusters (AuNCs) have been found to be correlated with both the size of the cluster and the flexibility of the Au–S framework. This newly identified PCET behavior in AuNCs is prominently different from that observed in semiconductor quantum dots and plasmonic metal nanoparticles. Our findings are of crucial importance for unveiling the catalytic mechanisms of quantum-confined metal nanomaterials and for the future rational design of more efficient catalysts.
研究领域:
材料科学
·
化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Biosensors-Basel
·
2022
·Vol. 12
·期 11
·988
·
IF 5.743
Linmin Chen,Meihuang Zeng,Jingwen Jin,Qiuhong Yao,Tingxiu Ye,Longjie You,Xi Chen,Xiaomei Chen,Zhiyong Guo
Nanoenzyme reactors based on shell-isolated colloidal plasmonic nanomaterials are well-established and widely applied in catalysis and surface-enhanced Raman scattering (SERS) sensing. In this study, a “double wing with one body” strategy was developed to establish a reduced food antiseptic sensing method using shell-isolated colloidal plasmonic nanomaterials. Gold nano particles (Au NPs) were used to synthesize the colloidal plasmonic nanomaterials, which was achieved by attaching ferrous ions (Fe2+), ferric ions (Fe3+), nitroso (NO−) group, cyanogen (CN−) group, and dopamine (DA) via coordinative interactions. The oxidation-induced reaction was utilized to generate •OH following the Fe2+-mediated Fenton reaction with the shell-isolated colloidal plasmonic nanomaterials. The •OH generated in the cascade reactor had a high oxidative capacity toward acid preservatives. Importantly, with the introduction of the signal molecule DA, the cascade reactor exhibited also induced a Raman signal change by reaction with the oxidation product (malondialdehyde) which improved the sensitivity of the analysis. In addition, the stable shell-isolated structure was effective in realizing a reproducible and quantitative SERS analysis method, which overcomes previous limitations and could extend the use of nanoenzymes to various complex sensing applications.
研究领域:
分析化学
·
纳米生物学
·
食品科学
✓ 已验证
DOI
高影响因子
ACS Applied Materials & Interfaces
·
2014
·
IF 5.9
Shaoyan Wang,Chunyu Liu,Hailong Wang,Gang Chen,Ming Cong,Wei Song,Qiong Jia,Shuping Xu,Weiqing Xu
A surface-enhanced Raman scattering (SERS)-active optical fiber sensor combining the optical fiber waveguide with various SERS substrates has been a powerful analytical tool for in situ and long-distance SERS detection with high sensitivity. The design and modification of a high-quality SERS-active sensing layer are important topics in the development of novel SERS-active optical fiber sensors. Here, we prepared a highly sensitive SERS-active optrode by in situ fabrication of a three-dimensional porous structure on the optical fiber end via a photoinduced polymerization reaction, followed by the growth of photochemical silver nanoparticles above the porous polymer material. The fabrication process is rapid (finished within 1 h) and can be on line under light control. The porous structure supports vast silver nanoparticles, which allows for strong electromagnetic enhancement of SERS. Interestingly, the preparation of this SERS optrode and its utilization for SERS detection can all be conducted in a microfluidic chip. The qualitative and quantitative on-chip SERS sensing of organic pollutants and pesticides has been achieved by this SERS optrode-integrated microfluidic chip, and its high detection sensitivity makes it a promising factor in the analysis of liquid systems.
研究领域:
分析化学
·
光学传感
·
环境监测
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Nature Communications
·
2024
·Vol. 15
·期 1
·1-12
·
IF 14.7
Cai Zhengwei,Liang Jie,Li Zixiao,Yan Tingyu,Yang Chaoxin,Sun Shengjun,Yue Meng,Liu Xuwei,Xie Ting,Wang Yan,Li Tingshuai,Luo Yongsong,Zheng Dongdong,Liu Qian,Zhao Jingxiang,Sun Xuping,Tang Bo
Electrocatalytic H 2 production from seawater, recognized as a promising technology utilizing offshore renewables, faces challenges from chloride-induced reactions and corrosion. Here, We introduce a catalytic surface where OH – dominates over Cl – in adsorption and activation, which is crucial for O 2 production. Our NiFe-based anode, enhanced by nearby Cr sites, achieves low overpotentials and selective alkaline seawater oxidation. It outperforms the RuO 2 counterpart in terms of lifespan in scaled-up stacks, maintaining stability for over 2500 h in three-electrode tests. Ex situ / in situ analyses reveal that Cr(III) sites enrich OH – , while Cl – is repelled by Cr(VI) sites, both of which are well-dispersed and close to NiFe, enhancing charge transfer and overall electrode performance. Such multiple effects fundamentally boost the activity, selectively, and chemical stability of the NiFe-based electrode. This development marks a significant advance in creating durable, noble-metal-free electrodes for alkaline seawater electrolysis, highlighting the importance of well-distributed catalytic sites.
研究领域:
电化学
·
材料科学
·
可再生能源
✓ 已验证
产品关联
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）