Building Blocks Research Articles

Aiming, Pointing, Steering: A Core Task Analysis Framework for Gameplay

Underneath their compelling audiovisual surface, games require players to carry out mundane interaction work, such as pointing, typing, or steering. However, many of these underlying building blocks are not defined rigorously, hampering synthesis and analysis. We elaborate on the origin of tasks within human-computer interaction (HCI) and define tasks' relationship to game terminology (game mechanics, goals, and actions). Our proposed framework draws on systemic-structural theory of activity to aid systematic analysis and exploration of game design by mapping gameplay to abstract core tasks. The framework contains four task tools, applicable when 1) uncovering design properties, 2) designing experimental manipulation, 3) creating behavioral measurements, and 4) describing gameplay in literature reviews of game genres and design techniques. We evaluated our framework as a lens to design purposeful games in three case studies within a scientific education. We invite researchers and practitioners to employ the framework as a microscope, to describe and design games rigorously.

Isolable Si=B Analogue of a Vinyl Halide: A Building Block for Facile Access toward Silicon‐Boron Multiple Bonded Species

AbstractCompared to the outstanding development in the synthesis of Si−B single bonded species, borylsilanes and their application to organic synthesis, the chemistry of Si=B double bonded species, borasilenes and boratasilenes have only made little progress, first of all, due to the difficulties in accessing such double bonds. Herein we report the synthesis of the first Si=B analogue of a vinyl halide, a bromoboratasilene, via formal borylene insertion to the coordination sphere of a monoatomic Si(0) complex, using a dihaloborane as the borylene source. The treatment of bromoboratasilene toward neutral or anionic Lewis bases gives access to new boratasilenes, all of which were proved to possess significant Si=B double bond character by XRD analysis and DFT calculations. These results demonstrate exciting strategies to synthesize new types of Si=B double bonded species which should further progress the chemistry of boron, silicon‐containing molecules.

Interactive Segmentation for Medical Images Using Spatial Modeling Mamba

Interactive segmentation methods utilize user-provided positive and negative clicks to guide the model in accurately segmenting target objects. Compared to fully automatic medical image segmentation, these methods can achieve higher segmentation accuracy with limited image data, demonstrating significant potential in clinical applications. Typically, for each new click provided by the user, conventional interactive segmentation methods reprocess the entire network by re-inputting the click into the segmentation model, which greatly increases the user’s interaction burden and deviates from the intended goal of interactive segmentation tasks. To address this issue, we propose an efficient segmentation network, ESM-Net, for interactive medical image segmentation. It obtains high-quality segmentation masks based on the user’s initial clicks, reducing the complexity of subsequent refinement steps. Recent studies have demonstrated the strong performance of the Mamba model in various vision tasks; however, its application in interactive segmentation remains unexplored. In our study, we incorporate the Mamba module into our framework for the first time and enhance its spatial representation capabilities by developing a Spatial Augmented Convolution (SAC) module. These components are combined as the fundamental building blocks of our network. Furthermore, we designed a novel and efficient segmentation head to fuse multi-scale features extracted from the encoder, optimizing the generation of the predicted segmentation masks. Through comprehensive experiments, our method achieved state-of-the-art performance on three medical image datasets. Specifically, we achieved 1.43 NoC@90 on the Kvasir-SEG dataset, 1.57 NoC@90 on the CVC-ClinicDB polyp segmentation dataset, and 1.03 NoC@90 on the ADAM retinal disk segmentation dataset. The assessments on these three medical image datasets highlight the effectiveness of our approach in interactive medical image segmentation.

An Improved Synthesis of 2,3-Diamino-5,6-dichloropyrazine: A Useful Heterocyclic Scaffold

Abstract2,3-Diamino-5,6-dichloropyrazine represents a valuable but underexplored heterocyclic building block. Due to the use of harsh conditions and lack of selectivity surrounding the known literature synthesis, we developed a more accessible and selective three-step route from 2-aminopyrazine. Challenging conditions are avoided by using a high-yielding dichlorination with N-chlorosuccinimide (NCS), which is followed by a regioselective amination. The installation of the last chlorine atom using 1-chloro-1,2-benziodoxol-3(1H)-one is rapid, enabling access to 2,3-diamino-5,6-dichloropyrazine in an improved overall yield (41%).

Step-by-Step Towards Biological Homochirality - from Prebiotic Randomness To Perfect Asymmetry.

The history of life's formation and the origin of its stereochemistry are nearly as multifaceted as the life itself. In this review, we focus on analyzing the step-by-step path leading to what we can define as "life" in parallel to what we know about the emergence of enantiomeric imbalance and subsequent transition to full homochirality. We start at the level of assembly of the building blocks of life from inorganic molecules and build up to the polymerization and formation of nucleic acids and peptides. We report and analyze different theories at various stages of this development and try to elucidate the most plausible theory.

Deconstructing the geography of human impacts on species’ natural distribution

It remains unknown how species’ populations across their geographic range are constrained by multiple coincident natural and anthropogenic environmental gradients. Conservation actions are likely undermined without this knowledge because the relative importance of the multiple anthropogenic threats is not set within the context of the natural determinants of species’ distributions. We introduce the concept of a species ‘shadow distribution’ to address this knowledge gap, using explainable artificial intelligence to deconstruct the environmental building blocks of current species distributions. We assess shadow distributions for multiple threatened freshwater fishes in Switzerland which indicated how and where species respond negatively to threats — with negative threat impacts covering 88% of locations inside species’ environmental niches leading to a 25% reduction in environmental suitability. Our findings highlight that conservation of species’ geographic distributions is likely insufficient when biodiversity mapping is based on species distribution models, or threat mapping, without also quantifying species’ expected or shadow distributions. Overall, we show how priority actions for nature’s recovery can be identified and contextualised within the multiple natural constraints on biodiversity to better meet national and international biodiversity targets.

Standards for Data Space Building Blocks

Data spaces are conceptualised as a trusted and secure distributed data ecosystem through which to exchange resources in the Web. Several efforts define guidance toward data space implementation, such as reference architectures and frameworks. As yet, the proposed data space solutions do not provide common and mature implementation options yet, and this gap between concept and implementation risks confusing users and developers. However, well-recognised organisations have been developing solutions and standards that address interoperability and good data exchange practices for decades, especially in the domain of geospatial information and remote sensing. Therefore, this paper compares the available solutions, providing the mapping and integration of the proposed blueprints to available interoperable standards. This concrete mapping, followed by a discussion with experts, results in a proposal of integrated reference data space building blocks, and an overview of the related standards and solutions. It is designed to support the effective practical implementation of data spaces and to guide future solution developments. This work can form the base for effective collaboration among different organisations, clearly identifying their scopes. A key role is apparent for standards and use cases from the remote sensing and geospatial domains, which have achieved wide adoption and maturity over the past years.

The Anti-Cancer Stem Cell Properties of Copper(II)-Terpyridine Complexes with Attached Salicylaldehyde Moieties.

We report the synthesis, characterisation, and anti-breast cancer stem cell (CSC) properties of two copper(II)-terpyridine complexes with bidentate salicylaldehyde moieties (2-hydroxybenzaldehyde for 1 and 2-hydroxy-1-naphthaldehyde for 2). The copper(II)-terpyridine complexes 1 and 2 are stable in biologically relevant aqueous solutions and display micromolar potency towards breast CSCs. The most effective complex 1 is 5-fold and 6.6-fold more potent towards breast CSCs than salinomycin and cisplatin, respectively. The copper(II)-terpyridine complexes 1 and 2 also decrease the formation and viability of three-dimensionally cultured mammospheres within the micromolar range. Notably complex 1 is up to 7-fold more potent towards mammospheres than salinomycin or cisplatin. Mechanistic studies suggest that the copper(II)-terpyridine complexes 1 and 2 are able to readily enter breast CSCs, elevate intracellular reactive oxygen species levels, induce DNA damage (presumably by oxidative DNA cleavage), and evoke apoptosis that is independent of caspases. This study shows that the copper(II)-terpyridine motif is a useful building block for the design of anti-breast CSC agents and reinforces the therapeutic potential of copper coordination complexes.

Regioselective Oxidative Phenol Coupling by a Mushroom Unspecific Peroxygenase.

Bioactive dimeric (pre-)anthraquinones are ubiquitous in nature and are found in bacteria, fungi, insects, and plants. Their biosynthesis via oxidative phenol coupling (OPC) is catalyzed by cytochrome P450 enzymes, peroxidases, or laccases. While the biocatalysis of OPC in molds (Ascomycota) is well-known, the respective enzymes in mushroom-forming fungi (Basidiomycota) are unknown. Here, we report on the biosynthesis of the atropisomers phlegmacin A1 and B1 of the mushroom Cortinarius odorifer. The biosynthesis of these unsymmetrically 7,10'-homo-coupled dihydroanthracenones was heterologously reconstituted in the mold Aspergillus niger. Methylation of the parental monomer atrochrysone to its 6-O-methyl ether torosachrysone by the O-methyltransferase CoOMT1 precedes the regioselective homocoupling to phlegmacin, catalyzed by the enzyme CoUPO1 annotated as an "unspecific peroxygenase" (UPO). Our results reveal an unprecedented UPO reaction, thereby expanding the biocatalytic portfolio of oxidative phenol coupling beyond the commonly reported enzymes. The results show that Basidiomycota use peroxygenases to selectively couple aryls independently of and convergently to any other group of organisms, emphasizing the central role of OPC in natural processes.

2-Cyano-N-(2,5-dioxopyrrolidin-1-yl) acetamide as a building block for developing new azole and azine derivatives and assessing their biological properties

2-Cyano-N-(2,5-dioxopyrrolidin-1-yl) acetamide as a building block for developing new azole and azine derivatives and assessing their biological properties

Bond-centric modular design of protein assemblies.

We describe a modular bond-centric approach to protein nanomaterial design inspired by the rich diversity of chemical structures that can be generated from the small number of atomic valencies and bonding interactions. We design protein building blocks with regular coordination geometries and bonding interactions that enable the assembly of a wide variety of closed and opened nanomaterials using simple geometrical principles. Experimental characterization confirms successful formation of more than twenty multi-component polyhedral protein cages, 2D arrays, and 3D protein lattices, with a high (10-50 %) success rate and electron microscopy data closely matching the corresponding design models. Because of the modularity, individual building blocks can assemble with different partners to generate distinct regular assemblies, resulting in an economy of parts and enabling the construction of reconfigurable systems.

Efficient quantum-dot adder optimisation and analysis for future circuits

ABSTRACT In recent years, the rapid scaling of transistors has necessitated the exploration of advanced alternatives to Complementary metal oxide semiconductor(CMOS) technology for future progress. Quantum-dot cellular automata(QCA) technology has emerged as a promising solution, offering highly dense, high-speed, and low-power circuits. Among the critical digital building blocks, adder circuits play a crucial role in arithmetic and logic units. Consequently, optimising these circuits in terms of area, delay, and quantum cost is essential for the development of efficient designs. This paper presents effective multi-layer n-bit ripple carry adder(RCA) circuits, utilising full adder(FA) circuit. The outputs are generated in distinct layers and verified using the QCADesigner-Ev2.2 tool with bi-stable and coherence vector energy setups, employing Euler and Runge-Kutta methods.Additionally, the proposed designs are evaluated for various design metrics at three different scale factors(1,0.8889,and 0.7778), corresponding to cell sizes of 18 × 18 nm , 16 × 16 nm , and 14 × 14 nm respectively. The temperature’s impact on the average output polarisation of the FA is explored. The research demonstrates an n-bit-RCA surpassing existing designs with cost optimisations of 89.5%, 86%, and 90.3% for 4-bit,8-bit and 16-bit circuits, respectively. The paper also provides a thorough energy dissipation analysis for the proposed adder design.

Production of 1,4-butanediol through Clostridia C4 pathways

1,4-butanediol (1,4-BDO) is an important building block in the chemical industry that has been mainly produced from fossil fuels, but now biosynthesis of 1,4-BDO has received more and more attention due to environmental issues. The Clostridia C4 pathway produces an intermediate crotonyl-CoA which could be diverted to 1,4-BDO by 4-hydroxybutyryl-CoA dehydratase (4HBD). Here, we compared this pathway with other 1,4-BDO biosynthesis pathways and illustrated its potential advantages regarding cellular energy conservation and theoretical yield. Then, the feasibility of 1,4-BDO production in this way was tested by introducing a single 4HBD in Clostridium acetobutylicum that natively produced the C4 intermediate and a variety of aldehyde/alcohol dehydrogenases (AdhE). Five different 4HBD genes were screened and the Cbei-2100 gene from Clostridium beijerinckii was the most effective, producing 0.066 mg/mL of 1,4-BDO. To block the metabolic flux towards the main product butanol, disruption of butyryl-CoA dehydrogenase (Bcd) was tried but failed, while inactivation of its homologue (FAD/FMN-containing dehydrogenase, Fcd) obtained little effect. Alternatively, the electron-transferring flavoprotein EtfA coupled with Bcd was inactivated, and 1,4-BDO production was greatly increased to 0.182 mg/mL. In conclusion, this study demonstrated the feasibility of 1,4-BDO production through the Clostridia C4 pathway. Further blocking of the competing flux towards butanol would be effective to improve the production of in the future.

High-Data-Rate Modulators Based on Graphene Transistors: Device Circuit Co-Design Proposals

The multifunctionality feature of graphene field-effect transistors (GFETs) is exploited here to design circuit building blocks of high-data-rate modulators by using a physics-based compact model. Educated device performance projections are obtained with the experimentally calibrated model and used to choose an appropriate improved feasible GFET for these applications. Phase-shift and frequency-shift keying (PSK and FSK) modulation schemes are obtained with 0.6 GHz GFET-based multifunctional circuits used alternatively in different operation modes: inverting and in-phase amplification and frequency multiplication. An adequate baseband signal applied to the transistors’ input also serves to enhance the device and circuit performance reproducibility since the impact of traps is diminished. Quadrature PSK is also achieved by combining two GFET-based multifunctional circuits. This device circuit co-design proposal intends to boost the heterogeneous implementation of graphene devices with incumbent technologies into a single chip: the baseband pulses can be generated with CMOS technology as a front end of line and the multifunctional GFET-based circuits as a back end of line.

Primitive asteroids as a major source of terrestrial volatiles.

The origins of Earth's volatiles are debated. Recent studies showed that meteorites display unique mass-independent isotopic signatures of the volatile element Zn, suggesting that Earth's Zn originated from materials derived from different regions of the Solar System. However, these studies largely omitted meteorites from the differentiated planetesimals thought to represent the Earth's building blocks, which underwent melting and substantial volatile loss. Here, we characterize the mass-independent Zn isotope compositions of meteorites from such planetesimals. We incorporate these results in mixing models that aim to reproduce Earth's abundance and isotope compositions of Zn and other elements. Our results suggest that, while differentiated planetesimals supplied ~70% of Earth's mass, they provided only ~10% of its Zn. The remaining Zn was supplied by primitive materials that did not experience melting and associated volatile loss. Combined with other findings, our results imply that an unmelted primitive material is likely required to establish the volatile budgets of the terrestrial planets.

Cover Feature: From Meteorite to Life's Building Blocks: A possible Electrochemical Pathway to Amino Acids and Peptide Bonds (Chem. Eur. J. 57/2024)

Cover Feature: From Meteorite to Life's Building Blocks: A possible Electrochemical Pathway to Amino Acids and Peptide Bonds (Chem. Eur. J. 57/2024)

Recent Advances in Transition Metal-Catalyzed Ring-Opening Reaction of Aziridine

The smallest strained, saturated N-heterocycles, such as aziridine, can be a valuable building block in synthetic organic chemistry. Ring-opening reactions with various nucleophiles could be the most important strategy to synthesize various value-added molecular entities. Therefore, regioselective ring-opening reactions of aziridines with various heteroatomic nucleophiles and carbon nucleophiles establish a useful synthetic methodology to synthesize biologically relevant β-functionalized alkylamines. The regio-selective ring-opening of aziridines is highly dependent on the substrate combination, and stereochemical control is challenging for Lewis acid-promoted reactions. Therefore, the development of a robust, catalytic ring-opening process that assists in the accurate prediction of regioselectivity and stereochemistry is highly desirable. Consequently, a large number of publications detailing distinct methods for aziridine ring-opening reactions can be found in the literature. In this review, we discuss several transition metal catalyzed cross-coupling reaction protocols for the ring opening of substituted aziridines with various carbon nucleophiles.

Predictive Representations: Building Blocks of Intelligence.

Adaptive behavior often requires predicting future events. The theory of reinforcement learning prescribes what kinds of predictive representations are useful and how to compute them. This review integrates these theoretical ideas with work on cognition and neuroscience. We pay special attention to the successor representation and its generalizations, which have been widely applied as both engineering tools and models of brain function. This convergence suggests that particular kinds of predictive representations may function as versatile building blocks of intelligence.

Thermal Conductivity Measurement System for Functional and Structural Products

An automated system for measuring the thermal conductivity of functional and structural materials was developed. The main building blocks of the setup are the following: heating unit and cooling unit creating a heat flux gradient in the test sample; thermal resistances for temperature registration and control; and thermal pads for better contact between parts of the setup and the sample. The effect of the thermal conductivity of thermal pads and thermal resistances on the distribution of thermal fields in the developed setup was studied by computer modelling. A control software for the measuring setup was developed based on the hardware implementation of the steady-state Fourier’s law-based method for the determination of thermal conductivity. The stopping criterion for the setup control software is the equality of heat fluxes in the heating and cooling units, as well as the stability of the thermal conductivity coefficient readings. The testing and calibration of the device were carried out using a sample of pure aluminum (99.999 wt.% Al). It was found that the experimental value of the thermal conductivity coefficient of the aluminum sample at room temperature (T = 22 °C) is <λ> = 243 ± 3 W/m·K. This value of the thermal conductivity coefficient is consistent with the literature data and experimental values obtained by the laser flash method, which ranges within λ = 210–260 W/m·K.

Controllable 1,4-Palladium Aryl to Aryl Migration in Fused Systems─Application to the Synthesis of Azaborole Multihelicenes.

Herein, we report the first 1,4-Pd aryl to aryl migration/Miyaura borylation tandem reaction in fused systems. The Pd shift occurred in the bay region of the dibenzo[g,p]chrysene building blocks, giving rise to a thermodynamically controlled mixture of 1,8- and 1,9-borylated compounds that allowed the preparation of regioisomeric azaborole multihelicenes from the same starting material. The outcome of this synthesis can be controlled by the choice of reaction conditions, allowing the migration process to be turned off in the absence of an acetate additive and the target multiheterohelicenes to be prepared in a regioselective manner. The target compounds show bright green fluorescence in dichloromethane with emission quantum yields (Φ) of up to 0.29, |glum| values up to 2.7 × 10-3, and green or green-yellow emission in the solid state, reaching Φ of 0.22. Single crystal X-ray diffraction analyses gave insight into their molecular structures and the packing arrangement. Evaluation of aromaticity in these multihelicenes revealed a nonaromatic character of the 2H-1,2-azaborole constituent rings.