Low Replicative Stress Triggers Cell-Type Specific Inheritable Advanced Replication Timing

DNA replication timing (RT), reflecting the temporal order of origin activation, is known as a robust and conserved cell-type specific process. Upon low replication stress, the slowing of replication forks induces well-documented RT delays associated to genetic instability, but it can also generate RT advances that are still uncharacterized. In order to characterize these advanced initiation events, we monitored the whole genome RT from six independent human cell lines treated with low doses of aphidicolin. We report that RT advances are cell-type-specific and involve large heterochromatin domains. Importantly, we found that some major late to early RT advances can be inherited by the unstressed next-cellular generation, which is a unique process that correlates with enhanced chromatin accessibility, as well as modified replication origin landscape and gene expression in daughter cells. Collectively, this work highlights how low replication stress may impact cellular identity by RT advances events at a subset of chromosomal domains.     

Effect of the structure of Pt-Ru/C particles on COad monolayer vibrational properties and electrooxidation kinetics

In this paper, we combined FTIR spectroscopy and CO_ad stripping voltammetry to investigate CO_ad adsorption and electrooxidation on Pt-Ru/C nanoparticles. The Pt:Ru elemental composition and the metal loading were determined by ICP-AES. The X-ray diffraction patterns of the Pt-Ru/C indicated formation of a Pt-Ru (fcc) alloy. HREM images revealed an increase in the fraction of agglomerated Pt-Ru/C particles with increasing the metal loading and showed that agglomerated Pt-Ru/C nanoparticles present structural defects such as twins or grain boundaries. In addition, isolated Pt-Ru/C nanoparticles have similar mean particle size (ca. 2.5 nm) and particle size distributions whatever the metal loading. Therefore, we could determine precisely the effect of particle agglomeration on the CO_ad vibrational properties and electrooxidation kinetics. FTIR measurements revealed a main CO_ad stretching band at ca. , which we ascribed to a-top CO_ad on Pt domains electronically modified by the presence of Ru. As the metal loading increased, the position of this band was blue shifted by ca. 5 cm⁻¹ and a shoulder around 2005 cm⁻¹ developed, which was ascribed to a-top CO_ad on Ru domains. The reason for this was suggested to be the increasing size of Ru domains on agglomerated Pt-Ru/C particles, which lifts dipole-dipole coupling and allows two vibrational features to be observed (CO_ad/Ru, CO_ad/Pt). This is evidence that FTIR spectroscopy can be used to probe small chemical fluctuations of the Pt-Ru/C surface. Finally, we comment on the CO_ad electrooxidation kinetics. We observed that CO_ad was converted more easily into CO₂ as the metal loading, i.e. the fraction of agglomerated Pt-Ru/C nanoparticles, increased.     

Fluidized bed chemical vapor deposition of silicon on carbon nanotubes for Li-ion batteries

Silicon was deposited on balls of entangled multi-walled carbon nanotubes (CNT) with a mean diameter of several hundreds of microns, by Fluidized Bed Chemical Vapor Deposition from silane (SiH4). The weight total percentage of deposited silicon was between 30 and 70%, to test their efficacy in Li-ion battery anodes. TEM and SEM imaging revealed that silicon deposits were of the form of nanoparticles uniformly dispersed on the whole CNT surface. The diameter of these nanoparticles increases with the deposited silicon percentage from 18 to 36 nm whereas their density remains constant at 5 10(22) nanoparticles/g of CNT. This indicates a low affinity of chemical species born from silane pyrolysis with the CNT surface for nucleation. The increase of the silicon nanoparticles diameter leads to the decrease of the specific surface area and the porous volume of the balls, probably due to the filling of the pores of the CNT network by silicon. A slight increase of the mean diameter of the balls was observed for the two highest silicon percentages, certainly due to the ability of the CNT network to be deformed under the mechanical stress induced by the silicon nanoparticles growth.     

法国的绿道概念,孰新孰旧?

首先列举了国际理论界对绿道概念进行的诠释,研究工作的重点包含生态、社会经济及综合意义等不同方面,但共同目标是给绿道规划寻找具有可参考性的建议.对法国的绿道概念"特拉梅韦尔特(trame verte)"的演变进行了综述,详细阐述了法国绿道概念从出生、衰落、概念的回归,到今天概念中融和可持续发展的理念.城市中的环境问题和生物多样性的退化是贯穿在整个概念演变过程中的主要因素,并直接促生了法国对绿道概念进行立法.对这项立法的原创件和有效性的评估认为,从前所未有地将绿道概念写入法律的角度,这项法律是一项创新,但是由于立法是在区域层面,而不是当地的执行层面,从而对这项法律能否真正有效提出质疑.     

Application of stochastic multiattribute analysis to assessment of single walled carbon nanotube synthesis processes

The unprecedented uncertainty associated with engineered nanomaterials greatly expands the need for research regarding their potential environmental consequences. However, decision-makers such as regulatory agencies, product developers, or other nanotechnology stakeholders may not find the results of such research directly informative of decisions intended to mitigate environmental risks. To help interpret research findings and prioritize new research needs, there is an acute need for structured decision-analytic aids that are operable in a context of extraordinary uncertainty. Whereas existing stochastic decision-analytic techniques explore uncertainty only in decision-maker preference information, this paper extends model uncertainty to technology performance. As an illustrative example, the framework is applied to the case of single-wall carbon nanotubes. Four different synthesis processes (arc, high pressure carbon monoxide, chemical vapor deposition, and laser) are compared based on five salient performance criteria. A probabilistic rank ordering of preferred processes is determined using outranking normalization and a linear-weighted sum for different weighting scenarios including completely unknown weights and four fixed-weight sets representing hypothetical stakeholder views. No single process pathway dominates under all weight scenarios, but it is likely that some inferior process technologies could be identified as low priorities for further research.     

Indirect urea electrooxidation by nickel(III) in alkaline medium: From kinetic and mechanism to reactor modeling

This study consists in the determination of two kinetic laws of urea oxidation (UO) and electrooxidation (UEO) in alkaline media on nickel(III). Two kinds of active sites were examined, the first one derived from a Ni(OH)₂ powder and the second from a massive nickel electrode. Partial orders of nickel(III) (two for UO and five UEO) enable to conclude about (i) the urea adsorption on two nickel(III) sites and (ii) that a multistep oxidation of urea occurs involving five nickel(III) site electroregenerations. A multipathway mechanism is also proposed to explain UEO facilitated by the nickel(III)/nickel(II) mediation system, and to predict the by-products' formation previously identified ($\mathrm{N}{\mathrm{O}}_2^{-},\mathrm{N}{\mathrm{H}}_3,\mathrm{OC}{\mathrm{N}}^{-},\mathrm{C}{\mathrm{O}}_3^{2-}$). At last, a model combining the UEO kinetic law previously established, with diffusive and convective transport phenomena was developed. A consistent correlation (maximum deviation of 6%) between laboratory electrolysis results with the model' predictions was obtained under different operating conditions, enabling the validation of this model.     

Strained Dehydrogenative Ring Closure of Phenylcarbazoles

What does it take to force a rigid and strained dehydrogenative ring closure, for example, in phenylcarbazoles? Since the works of Buchwald and Fagnou, palladium‐catalysed ring‐closing dehydrogenative reactions are legion, but will not operate when the strain at the reductive elimination stage becomes too large. We propose here a “muscled up” super‐oxidative palldium‐catalysed C H activation method for the ring closure of strained phenylcarbazoles.

     

Tensile and water barrier properties of cassava starch composite films reinforced by synthetic zeolite and beidellite

Composites films were prepared by the casting method using native cassava starch plasticized with glycerol and 3D or 2D synthetic fillers i.e. Beta zeolite and Na-beidellite type 2:1 phyllosilicate. Special attention was paid to the effect of the filler contents and type on the mechanical and barrier properties. It was shown that films reinforced with lyophilized Beta zeolite presented both high water solubility (WS) and water vapor permeability (WVP) values than the pristine starch whereas an improvement on the WVP was found for composites prepared from Na-beidellite or from non lyophilized Beta zeolite. For the two types of fillers, a drastic increase of the mechanical properties (especially in the Young’s modulus) was observed.     

η-Carbides (Co,Mo, or W) Nanoparticles from Octacyanometalates Precursors-Based Network

This paper describes a simple, two-steps chemical pathway to obtain bimetallic carbide nanoparticles (NPs) of general formula MxM″yC, also called η-carbides. This process allows for a control of the chemical composition of metals present in the carbides (M = Co and M″ = Mo or W). The first step involves the synthesis of a precursor consisting of a network of octacyanometalates. The second step consists in a thermal degradation of the previously obtained octacyanometalates networks under neutral atmosphere (Ar or N₂). It is shown that this process results in the formation of carbide NPs with diameter of ≈ 5nm, and the stoichiometries Co₃M’₃C, Co₆M’₆C, Co₂M’₄C for the Cs Co M’ systems.