基于故事情景链语法的偶动画短片分析与建模

偶动画是动画领域一个重要的分支，与传统手绘动画同步出现，甚至更早。偶动画作品以其独特的拍摄方法和艺术魅力，为众多艺术家和观众所喜爱。偶动画影片设计周期长、工作量大、生产过程复杂、经济风险高，用传统手工工艺制作完成一部5 min的定格动画影片，通常需要数年。本文以丹麦知名动画导演克里多夫·皮拉丹的《柏树山上的风》及德国格里高利·祖坎导演的《龙焰火枪》为例，提出以故事情节(storyline(i)),?i∈1,2,…,n?与情景链（scenario?chain）语法有限集的形式语言表达式分解偶动画电影的故事元素，通过叙事空间（narrative?space）中镜头画面的组接逻辑，形成不同叙事结构，以分析定格动画电影的故事寓意（implied?meaning），从故事计算的角度将其转化为标准化设计流程，为构建偶动画电影故事建模理论以及辅助智能计算提供思路，方法提高了偶动画电影的设计与制作效率，为多学科协同创作提供了新模式，使普通偶动画爱好者也能参与创作。     

Study on backward-facing step flow and heat transfer characteristics of hybrid nanofluids

Journal of Thermal Analysis and Calorimetry - As high heat dissipation has increasingly become the primary factor restricting the capability of electronic elements, and the high temperature of the...     

Delay driven Hopf bifurcation and chaos in a diffusive toxin producing phytoplankton‐zooplankton model

This paper deals with a diffusive toxin producing phytoplankton‐zooplankton model with maturation delay. By analyzing eigenvalues of the characteristic equation associated with delay parameter, the stability of the positive equilibrium and the existence of Hopf bifurcation are studied. Explicit results are derived for the properties of bifurcating periodic solutions by means of the normal form theory and the center manifold reduction for partial functional differential equations. Numerical simulations not only agree with the theoretical analysis but also exhibit the complex behaviors such as the period‐3, 5, 6, 7, 8, 11, and 12 solutions, cascade of period‐doubling bifurcation in period‐2, 4, quasi‐periodic solutions, and chaos. The key observation is that time delay may control harmful algae blooms (HABs). Moreover, numerical simulations show that the chaotic states induced by the period‐doubling bifurcation are purely temporal, which is stationary in space and oscillatory in time. The investigations may provide some new insights on harmful phytoplankton blooms.     

Palladium‐catalyzed unstrained C(sp3)―N bond activation: the synthesis of N,N‐dimethylacetamide by carbonylation of trimethylamine

This work describes a highly efficient unstrained C(sp³)―N bond activation approach for synthesis of N,N‐dimethylacetamide (DMAc) via catalytic carbonylation of trimethylamine using a PdCl₂/bipy (bipy = 2,2′‐bipyridine)/Me₄NI catalyst system. A low Pd catalyst dosage (1.0 mol%) is sufficient for high selectivity (98.1%) and yield (90.8%), with a turnover number (TON) of 90.0 mmol of DMAc obtained per mmol of PdCl₂ employed under mild reaction conditions. The influence of reaction parameters such as catalyst precursor dosage, ligand type and promoter on activity is investigated. This work also discusses in detail the halide promoter's role in the reaction, and provides a plausible mechanism based on the intermediates methyl iodide and acetyl iodide. Analyses indicate that the carbonylation of trimethylamine may proceed through an active intermediate acetyl iodide formed by carbonylation of methyl iodide generated from the decomposition of the promoter Me₄NI under reaction conditions. The formation of acetyl iodide favors the cleaving efficiency of the inert unstrained C(sp³)―N bond of trimethylamine. Copyright © 2013 John Wiley & Sons, Ltd.     

Mode selectivity of multisegment composite-cavity semiconductor lasers

The single longitudinal mode (SLM) characteristics of narrow linewidth long-external-cavity semiconductor lasers has been improved significantly by using a multisegment composite-cavity configuration. In this paper, the mode selectivities of two-segment, three-segment and four-segment cavity semiconductor lasers have been analysed and compared. In experiments, a four-segment composite cavity laser exhibits SLM oscillation with side-mode suppression ratio of 30 dB even for total external cavity length of 75 cm. The oscillation linewidth is less than 200 kHz.     

Complexes of Li atoms with formaldehyde (LiOCH2) and formaldimine (LiNHCH2): stability via electrostatic and charge transfer interactions

The Li atom adducts of formaldehyde (LiOCH₂) and formaldimine (LiNHCH₂) are produced in the gas phase by neutralization of the corresponding cations. Subsequent reionization, ca. 0.3 μs later, shows that the nominally hypervalent complexes LiXCH₂ (X=O or NH) are stable, residing in potential energy minima. In the time span between the neutralization and reionization events, the LiXCH₂ molecules dissociate partly into their constituents, Li + XCH₂, the fragmentation extent of LiNHCH₂ being more extensive. Ab initio calculations reveal three bound states for both Li atom complexes. Two (states A and B) resemble C-centered radicals carrying an ion pair, Li⁺·⁻X---CH₂^·, and can be viewed as lithiated derivatives of the hydroxymethyl (HOCH₂^·) or aminomethyl (H₂NCH₂^·) radical; the third state (C) represents a conventional, electrostatically bonded Li---X=CH₂ complex with an essentially intact X=C double bond and the unpaired electron located at the metal atom. States A and B are bound more strongly than state C for LiOCH₂; the opposite is true for LiNHCH₂, where C is the most stable arrangement and B only marginally bound. The larger degree of dissociation observed for LiNHCH₂ vis à vis LiOCH₂ upon neutralization–reionization points out that the experiment samples a considerable amount of state B which is barely bound for LiNHCH₂.     

Additive–multiplicative hazards model with current status data

The additive–multiplicative hazards (AMH) regression model specifies an additive and multiplicative form on the hazard function for the counting process associated with a multidimensional covariate process, which contains the Cox proportional hazards model and the additive hazards model as its special cases. In this paper, we study the AMH model with current status data, where the cumulative hazard hazard function is assumed to be nonparametric and is estimated using B-splines with monotonicity constraint on the functional, while a simultaneous sieve maximum likelihood estimation is proposed to estimate regression parameters. The proposed estimator for the parameter vector is shown to be asymptotically normal and semiparametric efficient. The B-splines estimator of the functional of the cumulative hazard function is shown to achieve the optimal nonparametric rate of convergence. A simulation study is conducted to examine the finite sample performance of the proposed estimators and algorithm, and a real data example is presented for illustration.     

Dried polyacrylamide gel absorption: a method for efficient elimination of the interferences from SDS-solubilized protein samples in mass spectrometry-based proteome analysis

Sample preparation holds an important place in MS-based proteome analysis. For effective proteolysis and MS analysis, it is essential to eliminate the interferences while extracting the analytes of interest from complex mixtures. To address this, herein we describe a new dried polyacrylamide gel absorption method. In this method, the protein sample prepared using high concentration of SDS was directly and completely absorbed by vacuum-dried polyacrylamide gel, and then the interfering substances including SDS and some other salts were efficiently removed by in-gel washing steps while retaining the denatured proteins in the gel, thus offering a clean environment amenable to downstream buffer exchange, proteolytic digestion and digest recovery, etc. In combination with in-gel digestion and LC-MS/MS, the newly developed method was applied to the proteome analyses of membrane-enriched fraction and whole tissue homogenate. It was demonstrated that the method is suitable for the analysis of a complex biological sample and can be widely used for sample cleanup in shotgun proteome analyses.     

Effects of double substitution on the thermodynamic stabilities of nitrogen radicals

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Asymmetric synthesis of dihydro-1,3-dioxepines by Rh(ii)/Sm(iii) relay catalytic three-component tandem [4 + 3]-cycloaddition

Heterocycles have been widely used in organic synthesis, agrochemical, pharmaceutical and materials science industries. Catalytic three-component ylide formation/cycloaddition enables the assembly of complex heterocycles from simple starting materials in a highly efficient manner. However, asymmetric versions remain a yet-unsolved task. Here, we present a new bimetallic catalytic system for tackling this challenge. A combined system of Rh(ii) salt and chiral N,N′-dioxide–Sm(iii) complex was established for promoting the unprecedented tandem carbonyl ylide formation/asymmetric [4 + 3]-cycloaddition of aldehydes and α-diazoacetates with β,γ-unsaturated α-ketoesters smoothly, affording various chiral 4,5-dihydro-1,3-dioxepines in up to 97% yield, with 99% ee. The utility of the current method was demonstrated by conversion of products to optically active multi-substituted tetrahydrofuran derivatives. A possible reaction mechanism was provided to elucidate the origin of chiral induction based on experimental studies and X-ray structures of catalysts and products.

Catalytic asymmetric tandem carbonyl ylide formation/[4 + 3]-cycloaddition of β,γ-unsaturated α-ketoesters, aldehydes and α-diazoacetates was achieved by using a bimetallic rhodium(ii)/chiral N,N′-dioxide–Sm(iii) complex catalyst.