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Periodic Lateral Root Priming: What Makes It Tick? 周期性侧根引物:是什么让它熠熠生辉?
IF 11.6 Pub Date : 2017-03-01 Epub Date: 2017-02-21 DOI: 10.1105/tpc.16.00638
Marta Laskowski, Kirsten H Ten Tusscher

Conditioning small groups of root pericycle cells for future lateral root formation has a major impact on overall plant root architecture. This priming of lateral roots occurs rhythmically, involving temporal oscillations in auxin response in the root tip. During growth, this process generates a spatial pattern of prebranch sites, an early stage in lateral root formation characterized by a stably maintained high auxin response. To date, the molecular mechanism behind this rhythmicity has remained elusive. Some data implicate a cell-autonomous oscillation in gene expression, while others strongly support the importance of tissue-level modulations in auxin fluxes. Here, we summarize the experimental data on periodic lateral root priming. We present a theoretical framework that distinguishes between a priming signal and its subsequent memorization and show how major roles for auxin fluxes and gene expression naturally emerge from this framework. We then discuss three mechanisms that could potentially induce oscillations of auxin response: cell-autonomous oscillations, Turing-type patterning, and tissue-level oscillations in auxin fluxes, along with specific properties of lateral root priming that may be used to discern which type of mechanism is most likely to drive lateral root patterning. We conclude with suggestions for future experiments and modeling studies.

为未来侧根的形成调节小群根周细胞对整个植物根系结构有重大影响。侧根的这种启动是有节律地发生的,涉及根尖中辅助素反应的时间振荡。在生长过程中,这一过程会产生前分枝点的空间模式,这是侧根形成的早期阶段,其特点是稳定地维持高辅素反应。迄今为止,这种节律性背后的分子机制仍然难以捉摸。一些数据表明基因表达中存在细胞自主振荡,而另一些数据则有力地证明了组织水平调节在辅助素通量中的重要性。在此,我们总结了有关周期性侧根启动的实验数据。我们提出了一个理论框架,该框架区分了启动信号及其随后的记忆,并说明了从这个框架中自然产生的辅助素通量和基因表达的主要作用。然后,我们讨论了可能诱导辅素反应振荡的三种机制:细胞自主振荡、图灵型模式化和组织级辅素通量振荡,以及侧根启动的具体特性,这些特性可用来判别哪种机制最有可能驱动侧根模式化。最后,我们对未来的实验和建模研究提出了建议。
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引用次数: 0
Structural Effects of Magnesium Dialkoxides as Precursors for Magnesium-Ion Electrolytes 氧化镁作为镁离子电解质前驱体的结构效应
Pub Date : 2015-01-01 DOI: 10.1149/2.0031506EEL
J. Herb, Carl Nist-Lund, J. Schwartz, C. Arnold
A challenge for magnesium ion battery research is the development of electrolytes that are capable of reversible magnesium electrodeposition through multiple cycles. Magnesium alkoxide chlorides and aryloxide chlorides are known magnesium ion electrolytes when used in conjunction with aluminum chloride. Herein we report the effects of structural variation in several dialkoxy and diaryloxy magnesium complex aggregates with aluminum chloride, Mg(OR)2:AlCl3 (R = iPr, t-Bu, phenyl), on electrochemical characteristics of their solutions and on compositions of the magnesium-containing deposits they yield. We also report the synthesis of a magnesium phenoxide-based electrolyte directly from magnesium metal. © The Author(s) 2015. Published by ECS. This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 License (CC BY, http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse of the work in any medium, provided the original work is properly cited. [DOI: 10.1149/2.0031506eel] All rights reserved.
镁离子电池研究面临的一个挑战是开发能够通过多次循环可逆镁电沉积的电解质。当与氯化铝结合使用时,烷氧镁氯化物和芳酰氯化物是已知的镁离子电解质。本文报道了几种二氧基和二氧基镁与氯化铝、Mg(OR)2:AlCl3 (R = iPr, t-Bu, phenyl)络合聚集体的结构变化对其溶液的电化学特性及其产生的含镁沉积物组成的影响。我们还报道了直接以金属镁为原料合成了一种基于苯氧化镁的电解质。©作者2015。由ECS出版。这是一篇基于知识共享署名4.0许可(CC BY, http://creativecommons.org/licenses/by/4.0/)的开放获取文章,该许可允许在任何媒体上不受限制地重复使用该作品,前提是正确引用原始作品。[DOI: 10.1149/2.0031506]版权所有。
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引用次数: 7
Non-Equilibrium Li Insertion Paths in LiMn0.75Fe0.25PO4 Observed during the Relaxation Process LiMn0.75Fe0.25PO4弛豫过程中非平衡Li插入路径的观察
Pub Date : 2015-01-01 DOI: 10.1149/2.0031503EEL
Yoshinori Satou, S. Komine, S. Takai, T. Yao
We observed in detail the XRD profiles of LiMn0.75Fe0.25PO4 taken during the relaxation time. We founded the peak position of the Li-rich phase shifted to lower angles during the relaxation process. We also founded that the intensity around the midpoint between the peak positions of the Li-rich phase and that of the Li-lean phase decreased immediately after the lithium insertion and the delay of the decrease in the intensity around the Li-rich phase. We consider that these happened due to the crystal structure peculiar to the lithium manganese iron phosphate.
详细观察了弛豫时间内LiMn0.75Fe0.25PO4的XRD谱图。我们发现在弛豫过程中富锂的峰位置向低角度移动。我们还发现,在插入锂后,富锂相和贫锂相峰位中点附近的强度立即下降,富锂相周围强度下降的延迟。我们认为这是由于磷酸锰铁锂特有的晶体结构造成的。
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引用次数: 8
The Use of a Sintered Ag/AgCl Electrode as Both Reference and Counter Electrode for Electrochemical Measurements in Thin Film Electrolytes 烧结Ag/AgCl电极作为参考电极和反电极用于薄膜电解质的电化学测量
Pub Date : 2015-01-01 DOI: 10.1149/2.0051510EEL
P. Khullar, J. V. Badilla, R. Kelly
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引用次数: 15
Functional Nanostructure Engineering of SOFC Cathode by Solution Infiltration 溶液浸润SOFC阴极的功能纳米结构工程
Pub Date : 2015-01-01 DOI: 10.1149/2.0051503EEL
Shiwoo Lee, K. Gerdes
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引用次数: 5
Redox Behavior of Dopamine in the Presence of Ferritin 铁蛋白存在下多巴胺的氧化还原行为
Pub Date : 2015-01-01 DOI: 10.1149/2.0011506EEL
Jaroslav Vatrál, R. Boča
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引用次数: 0
Discharge/Charge Characteristics of Li-O2 Batteries Using Noble Metal Catalyst Supported on a Carbon-Free Al-Doped ZnO Cathode 无碳铝掺杂ZnO阴极负载贵金属催化剂对锂氧电池放电/充电特性的影响
Pub Date : 2015-01-01 DOI: 10.1149/2.0011510EEL
J. Jo, Mihye Wu, S. Nahm, Yongku Kang, Ha-Kyun Jung
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引用次数: 1
Suppression of CO Adsorption on PtRu/C and Pt/C with RuO2 Nanosheets RuO2纳米片抑制PtRu/C和Pt/C对CO的吸附
Pub Date : 2015-01-01 DOI: 10.1149/2.0011505EEL
Daisuke Takimoto, T. Ohnishi, W. Sugimoto
RuO2 nanosheets were studied as a promotor for the hydrogen oxidation reaction in the presence of 300 ppm CO/H2. The hydrogen oxidation current in 300 ppm CO/H2 for RuO2 nanosheet modified PtRu/C catalyst (RuO2:Pt:Ru = 0.5:1:1 (molar ratio)) exhibited higher CO tolerance than Pt1Ru1/C and Pt2Ru3/C. Based on hydrodynamic voltammetry, chronoamperometry and CO stripping voltammetry, the addition of RuO2 nanosheets is suggested to suppress CO adsorption on the catalyst surface, resulting in an improvement in CO tolerance. © The Author(s) 2015. Published by ECS. This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 License (CC BY, http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse of the work in any medium, provided the original work is properly cited. [DOI: 10.1149/2.0011505eel] All rights reserved.
在CO/H2浓度为300 ppm的条件下,研究了RuO2纳米片作为氢氧化反应的促进剂。在300 ppm CO/H2条件下,RuO2纳米片改性PtRu/C催化剂(RuO2:Pt:Ru = 0.5:1:1(摩尔比))的氢氧化电流比Pt1Ru1/C和Pt2Ru3/C表现出更高的CO耐受性。基于流体动力伏安法、计时伏安法和CO溶出伏安法,建议添加RuO2纳米片抑制CO在催化剂表面的吸附,从而提高CO耐受性。©作者2015。由ECS出版。这是一篇基于知识共享署名4.0许可(CC BY, http://creativecommons.org/licenses/by/4.0/)的开放获取文章,该许可允许在任何媒体上不受限制地重复使用该作品,前提是正确引用原始作品。[DOI: 10.1149/2.0011505]版权所有。
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引用次数: 12
A Critical Assessment of as a Figure of Merit for Oxygen Reduction Electrocatalysts in Aqueous Electrolytes 水电解质中氧还原电催化剂性能指标的关键评价
Pub Date : 2015-01-01 DOI: 10.1149/2.0021506EEL
N. Georgescu, Adriel Jebin Jacob Jebaraj, D. Scherson
Certain aspects of the interpretation of rotating ring-disk electrode, RRDE, data for the oxygen reduction reaction, ORR, in aqueous electrolytes have been examined. In particular, the classical mechanism proposed by Damjanovic et al. [J. Chem. Phys. 45, 4057 (1966)] predicts that at a fixed potential, a plot of the ratio of the disk to the ring currents for the ORR vs ω−1/2, where ω is the rotation rate of the disk, should be linear. According to this analysis, the slope of this line is proportional to k3/XH2O2 , where k3 is the rate constant for the reduction of solution phase hydrogen peroxide, H2O2(aq), and XH2O2 is the fraction of the disk current that generates H2O2(aq), the magnitude of which can be determined from the line intercept. Illustrations of this theoretical framework are provided for ORR data reported in the literature for experiments involving Pt-based electrodes and collected in our laboratories for Pt in aqueous acidic solutions. Critically emphasized is the need to perform ring-disk measurements at multiple rotations rates in order to determine reliable values of XH2O2 , which can be used as figures of merit for ranking the efficacy of ORR electrocatalysts. © The Author(s) 2015. Published by ECS. This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 License (CC BY, http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse of the work in any medium, provided the original work is properly cited. [DOI: 10.1149/2.0021506eel] All rights reserved.
对旋转环盘电极的某些方面的解释,RRDE,氧还原反应的数据,ORR,在水电解质中进行了检查。特别是Damjanovic等人提出的经典机制[J]。化学。物理学[Phys. 45,4057](1966)预测,在一个固定的电位下,圆盘与环电流的比值对于ORR vs ω−1/2的图,其中ω是圆盘的旋转速率,应该是线性的。根据这个分析,这条线的斜率与k3/XH2O2成正比,其中k3是液相过氧化氢H2O2的还原速率常数(aq), XH2O2是产生H2O2的磁碟电流的分数(aq),其大小可以从线截距确定。这一理论框架的插图提供了文献中涉及Pt基电极的实验报告的ORR数据,并在我们的实验室中收集了酸性水溶液中的Pt。需要强调的是,需要在多个旋转速率下进行环盘测量,以确定可靠的XH2O2值,该值可作为评价ORR电催化剂效率的指标。©作者2015。由ECS出版。这是一篇基于知识共享署名4.0许可(CC BY, http://creativecommons.org/licenses/by/4.0/)的开放获取文章,该许可允许在任何媒体上不受限制地重复使用该作品,前提是正确引用原始作品。[DOI: 10.1149/2.0021506]版权所有。
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引用次数: 9
Potential Oscillation Associated Galvanostatic Deposition of Periodic Al Wires from a Chloroaluminate Ionic Liquid 氯铝酸盐离子液体中周期性铝丝的电位振荡相关恒流沉积
Pub Date : 2015-01-01 DOI: 10.1149/2.0021507EEL
C. Su, I. Sun
Experimental All the electrochemical experiments were carried out in the quiescent AlCl3/TMHC (58/42 mol%) in a N2-filled glove box at 38 ◦ C using a conventional three-electrode cell. An Al spiral wire (Alfa Aesar, 99.95%) immersed in the bulk IL was used as the counter electrode, the reference electrode was an Al wire in a fritted glass tube filled with the same IL. The working electrode was a W wire (diameter =0.5 mm). The electrochemical experiments were performed with an EG&G PARC Model 263A potentiostat/galvanostat controlled with EG&G Model 270 software. High-resolution scanning electron microscopy (HITACHI, SU8000) was used to examine the morphology of the deposits.
所有电化学实验均在38◦C的氮气填充手套箱中使用传统的三电极电池,在静止的AlCl3/TMHC (58/42 mol%)中进行。用Al螺旋丝(Alfa Aesar, 99.95%)浸泡在大量IL中作为对电极,参比电极为Al丝,在填充相同IL的熔融玻璃管中,工作电极为W丝(直径=0.5 mm)。电化学实验采用EG&G PARC Model 263A恒电位器/恒电位器,由EG&G Model 270软件控制。采用高分辨率扫描电子显微镜(HITACHI, SU8000)检查沉积物的形貌。
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引用次数: 6
期刊
ECS Electrochemistry Letters
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