Cell Wall Regions Research Articles

Elucidating β-1,3-Glucanase and Peroxidase Physicochemical Properties of Wheat Cell Wall Defense Mechanism against Diuraphis noxia Infestation.

Wheat plants infested by Russian wheat aphids (RWA) induce a cascade of defense responses, including the hypersensitive responses (HR) and induction of pathogenesis-related (PR) proteins, such as β-1,3-glucanase and peroxidase (POD). This study aims to characterize the physicochemical properties of cell wall-associated POD and β-1,3-glucanase and determine their synergism on the cell wall modification during RWASA2-wheat interaction. The susceptible Tugela, moderately resistant Tugela-Dn1, and resistant Tugela-Dn5 cultivars were pregerminated and planted under greenhouse conditions, fertilized 14 days after planting, and irrigated every 3 days. The plants were infested with 20 parthenogenetic individuals of the same RWASA2 clone at the 3-leaf stage, and leaves were harvested at 1 to 14 days post-infestation. The Intercellular wash fluid (IWF) was extracted using vacuum filtration and stored at -20 °C. Leaf residues were crushed into powder and used for cell wall components. POD activity and characterization were determined using 5 mM guaiacol substrate and H2O2, monitoring change in absorbance at 470 nm. β-1,3-glucanase activity, pH, and temperature optimum conditions were demonstrated by measuring the total reducing sugars in the hydrolysate with DNS reagent using β-1,3-glucan and β-1,3-1,4-glucan substrates, measuring the absorbance at 540 nm, and using glucose standard curve. The pH optimum was determined between pH 4 to 9, temperature optimum between 25 and 50 °C, and thermal stability between 30 °C and 70 °C. β-1,3-glucanase substrate specificity was determined at 25 °C and 40 °C using curdlan and barley β-1,3-1,4-glucan substrates. Additionally, the β-1,3-glucanase mode of action was determined using laminaribiose to laminaripentaose. The oligosaccharide hydrolysis product patterns were qualitatively analyzed with thin-layer chromatography (TLC) and quantitatively analyzed with HPLC. The method presented in this study demonstrates a robust approach for infesting wheat with RWA, extracting peroxidase and β-1,3-glucanase from the cell wall region and their comprehensive biochemical characterization.

The Pivotal Role of Microscopy in Unravelling the Nature of Microbial Deterioration of Waterlogged Wood: A Review

This review focuses on the pivotal role microscopy has played in diagnosing the type(s) of microbial attacks present in waterlogged ancient wooden objects, and to understand the nature and extent of deterioration of such objects. The microscopic journey began with the application of light microscopy (LM) to examine the deterioration of waterlogged woods, notably foundation piles supporting historic buildings, progressing into the use of high-resolution imaging tools (SEM and TEM) and techniques. Although bacteria were implicated in the deterioration of foundation piles, confirmation that bacteria can indeed degrade wood in its native state came when decaying wood from natural environments was examined using electron microscopy, particularly TEM, which enabled bacterial association with cell wall regions undergoing degradation to be clearly resolved. The information base has been a catalyst, stimulating numerous studies in the past three decades or so to understand the nature of microbial degradation of waterlogged archaeological wood more precisely, combining LM, SEM, and TEM with high-resolution chemical analytical methods, including chemical microscopy. The emerging information is aiding targeted developments towards a more effective conservation of ancient wooden objects as they begin to be uncovered from burial and waterlogging environments.

NKS1/ELMO4 is an integral protein of a pectin synthesis protein complex and maintains Golgi morphology and cell adhesion in Arabidopsis

Adjacent plant cells are connected by specialized cell wall regions, called middle lamellae, which influence critical agricultural characteristics, including fruit ripening and organ abscission. Middle lamellae are enriched in pectin polysaccharides, specifically homogalacturonan (HG). Here, we identify a plant-specific Arabidopsis DUF1068 protein, called NKS1/ELMO4, that is required for middle lamellae integrity and cell adhesion. NKS1 localizes to the Golgi apparatus and loss of NKS1 results in changes to Golgi structure and function. The nks1 mutants also display HG deficient phenotypes, including reduced seedling growth, changes to cell wall composition, and tissue integrity defects. These phenotypes are comparable to qua1 and qua2 mutants, which are defective in HG biosynthesis. Notably, genetic interactions indicate that NKS1 and the QUAs work in a common pathway. Protein interaction analyses and modeling corroborate that they work together in a stable protein complex with other pectin-related proteins. We propose that NKS1 is an integral part of a large pectin synthesis protein complex and that proper function of this complex is important to support Golgi structure and function.

Super-stable modified wood for enhanced autonomous indoor humidity regulation

The crucial development of materials that automatically adjust indoor humidity, a significant factor in human health and daily life, has gained importance due to the emphasis on energy conservation. Wood, with its natural hygroscopic properties, is effective in this regard but faces challenges of deformation and cracking due to moisture content changes. Herein, we introduced an innovative in-situ wood modification strategy, which integrated deep eutectic solvent (DES) impregnation with heat treatment, producing dimensionally super-stable modified wood for enhanced autonomous indoor humidity regulation. This modification process focused on creating more robust cross-linking structures within the amorphous regions of the wood cell wall. As a result, water-induced deformation of natural wood was significantly reduced, as evidenced by an anti-swelling efficiency exceeding 80%, ensuring the long-term reliability of DES-modified wood in varying humidity environments. Additionally, the introduction of additional pores and hygroscopic sites in the cell wall enhanced the natural wood’s moisture buffering value by 2.5 times, showcasing the superior ability of DES-modified wood to control indoor humidity effectively. Moreover, the DES-modified wood also exhibited commendable flame retardancy and antibacterial properties. Consequently, this novel modified wood emerges as a reliable material for indoor humidity regulation, promoting healthier indoor conditions and offering a sustainable alternative for energy-efficient construction practices.

Chromosome-level genome assemblies of Musa ornata and Musa velutina provide insights into pericarp dehiscence and anthocyanin biosynthesis in banana.

Musa ornata and Musa velutina are members of the Musaceae family and are indigenous to the South and Southeast Asia. They are very popular in the horticultural market, but the lack of genomic sequencing data and genetic studies has hampered efforts to improve their ornamental value. In this study, we generated the first chromosome-level genome assemblies for both species by utilizing Oxford Nanopore long reads and Hi-C reads. The genomes of M. ornata and M. velutina were assembled into 11 pseudochromosomes with genome sizes of 427.85Mb and 478.10Mb, respectively. Repetitive sequences comprised 46.70% and 50.91% of the total genomes for M. ornata and M. velutina, respectively. Differentially expressed gene (DEG) and Gene Ontology (GO) enrichment analyses indicated that upregulated genes in the mature pericarps of M. velutina were mainly associated with the saccharide metabolic processes, particularly at the cell wall and extracellular region. Furthermore, we identified polygalacturonase (PG) genes that exhibited higher expression level in mature pericarps of M. velutina compared to other tissues, potentially being accountable for pericarp dehiscence. This study also identified genes associated with anthocyanin biosynthesis pathway. Taken together, the chromosomal-level genome assemblies of M. ornata and M. velutina provide valuable insights into the mechanism of pericarp dehiscence and anthocyanin biosynthesis in banana, which will significantly contribute to future genetic and molecular breeding efforts.

Bottom-up multiscale modelling of guard cell walls reveals molecular mechanisms of stomatal biomechanics

Abstract Stomata are dynamic pores on plant surfaces that regulate photosynthesis and are thus of critical importance for understanding and leveraging the carbon-capturing and food-producing capabilities of plants. However, our understanding of the molecular underpinnings of stomatal kinetics and the biomechanical properties of the cell walls of stomatal guard cells that enable their dynamic responses to environmental and intrinsic stimuli is limited. Here, we built multiscale models that simulate regions of the guard cell wall, representing cellulose fibrils and matrix polysaccharides as discrete, interacting units, and used these models to help explain how molecular changes in wall composition and underlying architecture alter guard wall biomechanics that gives rise to stomatal responses in mutants with altered wall synthesis and modification. These results point to strategies for engineering guard cell walls to enhance stomatal response times and efficiency.

Subgrain microstructural features in directed energy deposited stainless steel 316L: The influence of morphology on mechanical properties

Recent studies have established that the exceptional combination of strength and ductility of directed energy deposited stainless steel 316 L is primarily due to the barrier effect against mobile dislocations introduced by cellular subgrain feature boundaries. Interestingly, the morphology of the feature, and therefore its boundaries, exhibits a significant variation with process parameters. This article presents an experimental study to determine the mechanism responsible for the formation of cellular subgrain feature with different morphologies and the influence of morphology on mechanical properties. Two builds with cellular subgrain features of different morphologies, tubular and vermicular, are manufactured using different process parameters and scanning strategies. The microstructural analysis of the specimens shows very different element segregation and secondary phase distribution. The mechanism responsible for the formation of different morphologies is the differences in the solidification modes. The barrier effect has two contributions; a hard barrier effect introduced by delta ferrite secondary phases and a soft barrier effect introduced by austenite cell wall regions. Irrespective of different morphologies, the two builds exhibited similar macroscopic mechanical behavior. This indicates that the total barrier effect exerted by the cellular subgrain feature determines the mechanical properties of directed energy deposited stainless steel 316 L, not necessarily its morphology.

Revealing the structure and distribution changes of corn stalk lignin during the Organosolv Pretreatment

During the pretreatment of biomass, the research on the migration process of lignin in the cell wall and the change of chemical structure is very important for improving pretreatment and subsequent lignin upgrading. Hence, corn stalk lignin was extracted by 1, 4-dioxane organosolv system under mild conditions with varying pretreatment time and 0.1 M hydrochloric acid as catalyst. The heterogeneity of lignin removal in the different morphological areas of the cell wall was revealed by advanced imaging techniques. Results indicated that during the pretreatment with dioxane organosolv, the removal of lignin started from the secondary wall of the cell wall, and gradually developed outward to the compound middle lamella. Meanwhile, the resulting lignin obtained through different pretreatment times was characterized by two-dimensional heteronuclear single quantum coherence spectroscopy (2D-HSQC) and gel permeation chromatography (GPC). These characterization results indicated that there were more syringyl (S) units in the lignin that were removed first, and the proportion of guaiacyl (G) units was increased as the pretreatment continued. All the evidence supports the idea that the main reason for the significant differences in lignin structures at various periods of the lignin removal process is that the lignin come from different cell wall regions.

Molecular Cloning, Subcellular Localization, and Abiotic Stress Induction Analysis of a Polyamine Oxidase Gene from Oryza sativa

Abiotic stress is a major bottleneck for crop productivity. To counter abiotic stresses, plants have developed several strategies, and the accumulation of polyamine (PA) serving as an osmolyte is one of them. The cellular pool of PAs is primarily regulated by polyamine oxidases (PAOs) either by terminal catabolism or by back conversion (BC) of polyamines. The role of PAO in abiotic stress tolerance has also been reported. Polyamine oxidases are primarily localized in the cytosol, cell wall, and apoplastic regions; however, lately, their peroxisomal localization has also been demonstrated. In this study, we reported the detection of polyamine oxidase isoform 3 from Oryza sativa (OsPAO3) in peroxisome as early as 12 h post-transformation under in vitro conditions using fluorescent microscopy. The gene was also found to be significantly upregulated by salinity, dehydration, cold, and heat stress. We have also demonstrated that the expression of OsPAO3 gene was mediated by a second messenger, calcium. The upregulation of OsPAO3 by salinity, dehydration, cold, and heat stresses suggests that it could be a suitable candidate for providing tolerance to plants against abiotic stress combination or stress matrix, which is a common feature in agricultural field conditions. Furthermore, the data provided here would be valuable in understanding the abiotic stress-mediated signal transduction network of PAOs.

Cell corner middle lamella in hydroids of dendroid moss Hypnodendron menziesii gametophyte is prominently thickened: a proposed role in the mechanical support function.

Significantly thickened corner middle lamella of the hydroid cell wall in the stipe of dendroid moss Hypnodendron menziesii has a mechanical support function. The hydroid cell walls of the erect stipe of Hypnodendron menziesii were investigated using light microscopy (LM), transmission electron microscopy (TEM), and TEM-immunogold labeling in support of the proposed biomechanical function for the highly thickened cell corner middle lamellae. The statistical analyses of dimensions of hydroid cell and wall parameters revealed a strong positive correlation between the area of hydroid cell and (i) the hydroid cell walls adhering to thick corner middle lamella, (ii) the area of the thick cell wall at hydroid corners, and (iii) the maximum thickness of cell wall at hydroid corners. The total area of the thick cell wall at the hydroid corners concomitantly increased with the area of the hydroid cell wall adhering to the middle lamella, and with the increased number of hydroids surrounding a reference hydroid. The results suggest that markedly thickened middle lamellae of the hydroid cell wall in Hypnodendron likely function by preventing hydroid cells from collapsing under the tensile forces generated from the transpirational pull on the water column. The specific localization of (1→4)- β-D-galactan and (1,5)-α-L-arabinan in the interface region of the hydroid cell wall and the thick middle lamella is consistent with these cell wall components being involved in the mechanical strengthening of the interface through firm adhesion as well as elasticity, ensuring the structural stability of this cell wall region, which may be prone to delamination/fracturing from the various internal and external pressures imposed. The copious presence of homogalacturonan in the thick middle lamella may further enhance the strength and flexibility of hydroid cell walls.

Chemical and morphological modification of softwood and hardwood surfaces by an oxygen glow discharge plasma

High-energy radiation preferentially degrades cellulose and enriches lignin content at wood surfaces particularly in hardwoods. Accordingly, we hypothesize that a similar effect will occur at surfaces exposed to plasma. We test this hypothesis by plasma-treating pine and poplar veneers and assessing changes in the lignin and holocellulose-derived sugar-content of veneers; quantifying etching of pellets containing lignin and cellulose, and observing etching of different cell wall layers in pine and Homalium. The majority but not all of our results support our hypothesis. Lignin-rich regions of wood cell walls were easier to see after plasma treatment. We discuss the potential uses of plasma-etching for the study of wood ultrastructure and the creation of wood surfaces with self-bonding properties, and conclude that plasma-etching can be used as an alternative to chemical pretreatments for ultrastructural studies of the distribution of lignin in wood cell walls.

Exploration of deep eutectic solvent-based biphasic system for furfural production and enhancing enzymatic hydrolysis: Chemical, topochemical, and morphological changes

Developing a biorefinery process for a highly integrated valorization and fractionation of lignocellulose is crucial for its utilization. Herein, a biphasic system comprising choline chloride/lactic acid and 2-methyltetrahydrofuran with Al2(SO4)3 and H2SO4 as catalysts was applied to pretreat Eucalyptus. Results showed that under the optimized conditions (150 °C, 30 min, 0.2 M Al2(SO4)3, 0.075 M H2SO4), the furfural yield and enzymatic hydrolysis efficiency could reach 54.7% and 97.0%, respectively. The efficient cellulose conversion was attributed to remarkable removal of lignin (91.0%) and hemicelluloses (100.0%), thereby causing the disruption of cell wall structure and enhancement of cellulose accessibility. Meanwhile, confocal Raman microscope and atomic force microscope displayed that the pretreatment resulted in the decreasing intensities of carbohydrates and lignin different regions of cell walls, and exposing of the embedded microfibers from noncellulosic polymers. Overall, the deep eutectic solvent-based biphasic system displayed high performance for effective utilization of carbohydrate components in lignocellulose.

Comparative study of the effects of thermal blanching pretreatments and puffing temperature levels on the microstructure and qualities of crisp banana slices

AbstractApplying a high‐temperature and short‐time (HTST) puffing techniques is one way to produce fat‐free crisp snacks. However, the crisp snack products obtained via HTST tend to be browner with some scorching on their surface but several thermal blanching pretreatments can be used to limit such surface browning. Therefore, in this study, the effects of thermal blanching pretreatments and puffing temperature levels on the microstructure, drying time, and the qualities of crisp banana were investigated. Banana slices (2.5 mm thickness) were blanched by hot water, steam, and microwave pretreatments as well as dried by hot air at temperature of 90°C combined with hot air puffing in temperature ranges 150–190°C. The blanching pretreatments significantly limited browning and improved the uniformity of crisp product color. The hot water or steam pretreatments caused pronounced cells damage and swelling of the cell wall region, whereas the microwave pretreatment may have increased the cell wall strength of banana. Such differences in morphological structure resulted in a larger volume ratio and more crisp texture for the hot water‐ or steam‐pretreated bananas, yet different results were also observed for the microwave‐pretreated banana. The longest processing time of 367.0 min was observed on the microwave‐pretreated sample coupled with the lowest puffing temperature, 150°C. Therefore, appropriate either a pretreatment with hot water or steam together with puffing temperature of 170°C is recommended for banana processing to make crisps.Practical ApplicationsThe Namwa banana is commonly consumed as a fresh banana but it also rapidly deteriorates after harvesting. Therefore, it has been processed using several drying techniques to extend its shelf life and increase its market value. Novel drying techniques such as high‐temperature and short‐time (HTST) puffing could produce fat‐free crisp snack, especially given that this economical drying process and simple drying equipment required are well suited to small‐ and medium‐manufacturing enterprises. Nevertheless, via HTST, the crisp banana product undergoes more intensive browning and becomes nonuniform in color. Thermal blanching pretreatments are also required for banana processing because these could limit the browning and improved the uniformity of crisp banana color. The information gained in this study should be useful for the development of thermal blanching‐assisted drying of crisp banana at the small‐ and medium‐enterprise scale of production.

Variations in bacterial decay between cell types and between cell wall regions in waterlogged archaeological wood excavated in the intertidal zone

Abstract The bacterial decay of waterlogged archeological wood (WAW, hard pine spp.) taken from Daebudo shipwreck No. 2, which was buried in the intertidal zone in the mid-west coast (Yellow sea) of South Korea approximately 800 years ago, was investigated. The maximum moisture content of the outer parts (approx. 3 cm of depth) of WAW was approximately 4.2 times higher than that of undegraded reference pine wood. ATR-FTIR and solid-state 13C-NMR analysis indicated a relative increase of the lignin concentration in WAW caused by the degradation of cellulose and hemicelluloses across the board studied (31-cm-wide and 14.5-cm-thick board). Micromorphological studies also revealed that bacterial degradation was progressed to a depth of 15 cm (vertically 7.3 cm) from the surface, which is the innermost part of the board. Erosion bacteria (EB) were identified as the main degraders of WAW. Degradation by tunneling bacteria (TB) was occasionally detected. Decay resistance to bacterial attacks in WAW varied between cell types and between cell wall regions. Axial tracheids showed less resistance than ray tracheids, ray parenchyma cells, and axial intercellular canal cells, including strand tracheids, subsidiary parenchyma cells, and epithelial cells. Decay resistance was higher in ray tracheids and strand tracheids than in ray parenchyma cells and subsidiary parenchyma-/epithelial cells, respectively. Bordered- and cross-field pit membranes and the initial pit borders showed higher decay resistance than the tracheid cell walls. Overall, the S2 layer of the axial tracheids showed the weakest resistance to bacterial attacks.

Correlative Super-Resolution Optical and Atomic Force Microscopy Reveals Relationships Between Bacterial Cell Wall Architecture and Synthesis in Bacillus subtilis.

Understanding how bacteria grow and divide requires insight into both the molecular-level dynamics of ultrastructure and the chemistry of the constituent components. Atomic force microscopy (AFM) can provide near molecular resolution images of biological systems but typically provides limited chemical information. Conversely, while super-resolution optical microscopy allows localization of particular molecules and chemistries, information on the molecular context is difficult to obtain. Here, we combine these approaches into STORMForce (stochastic optical reconstruction with atomic force microscopy) and the complementary SIMForce (structured illumination with atomic force microscopy), to map the synthesis of the bacterial cell wall structural macromolecule, peptidoglycan, during growth and division in the rod-shaped bacterium Bacillus subtilis. Using “clickable” d-amino acid incorporation, we fluorescently label and spatially localize a short and controlled period of peptidoglycan synthesis and correlate this information with high-resolution AFM of the resulting architecture. During division, septal synthesis occurs across its developing surface, suggesting a two-stage process with incorporation at the leading edge and with considerable in-filling behind. During growth, the elongation of the rod occurs through bands of synthesis, spaced by ∼300 nm, and corresponds to denser regions of the internal cell wall as revealed by AFM. Combining super-resolution optics and AFM can provide insights into the synthesis processes that produce the complex architectures of bacterial structural biopolymers.

Cuticular wax composition contributes to different strategies of foliar water uptake in six plant species from foggy rupestrian grassland in tropical mountains

The cuticle is the outermost region of the epidermal cell wall of plant aerial organs. The cuticle acts as a two-way lipid barrier for water diffusion; therefore, it plays a vital role in foliar water uptake (FWU). We hypothesised that the chemical composition of the cuticular waxes influences the FWU strategy that plants adopt in a foggy tropical ecosystem. We analysed the leaf cuticular waxes of six plant species known by their different FWU strategies, in both qualitative and quantitative approaches, to test this hypothesis. We also investigated the fine structure of the plant cuticle by scanning electron microscopy. Neither the total wax loads nor the amounts of single wax compound classes correlated to the FWU. In contrast, the qualitative chemical composition of the cuticular waxes was related to the water absorption speed but not to the maximum water absorbed. The presence of wax crystals might interfere with the FWU. Our findings suggest that a complex three-dimensional network of the cuticular compounds contributes to different strategies of FWU in six plant species from foggy tropical mountaintops.

Raman imaging of Micrasterias: new insights into shape formation

The algae Micrasterias with its star-shaped cell pattern is a perfect unicellular model system to study morphogenesis. How the indentations are formed in the primary cell wall at exactly defined areas puzzled scientists for decades, and they searched for chemical differences in the primary wall of the extending tips compared to the resting indents. We now tackled the question by Raman imaging and scanned in situ Micrasterias cells at different stages of development. Thousands of Raman spectra were acquired from the mother cell and the developing semicell to calculate chemical images based on an algorithm finding the most different Raman spectra. Each of those spectra had characteristic Raman bands, which were assigned to molecular vibrations of BaSO4, proteins, lipids, starch, and plant cell wall carbohydrates. Visualizing the cell wall carbohydrates revealed a cell wall thickening at the indentations of the primary cell wall of the growing semicell and uniplanar orientation of the cellulose microfibrils to the cell surface in the secondary cell wall. Crystalline cellulose dominated in the secondary cell wall spectra, while in the primary cell wall spectra, also xyloglucan and pectin were reflected. Spectral differences between the indent and tip region of the primary cell wall were scarce, but a spectral mixing approach pointed to more cellulose fibrils deposited in the indent region. Therefore, we suggest that cell wall thickening together with a denser network of cellulose microfibrils stiffens the cell wall at the indent and induces different cell wall extensibility to shape the lobes.

Characterization of the structural and dynamic changes of cell wall obtained by ultrasound-water and ultrasound-alkali treatments

It is well-known that ultrasound has been studied for its cavitation, mechanical and thermal effects. As a pretreatment technology, ultrasonic alkali treatment has attracted much attention in the field of biomass biochemical transformation. In this study, the structural and dynamic changes of wood cell walls during ultrasound-water, alkali, and ultrasound-alkali treatments were investigated by stereoscopic microscopy, confocal Raman microscopy, Fourier-transform infrared spectroscopy, and X-ray diffraction. The results indicated that the ultrasound-water, alkali, and ultrasound-alkali treatments had the effect of removing extractives from conduits. The uniform self-shrinking samples with shrinkage conduits were obtained by the alkali and ultrasound-alkali treatments. All of the treatments affected the relative content, structure and distribution of the chemical components in the wood cell walls. Compared with water-immersion samples, the relative content of hemicellulose of the treated samples reduced from 32.31% to 7.02% for ultrasound-8% NaOH treated samples. For the signal intensity of lignin, ultrasound-water treated and ultrasound-alkali treated samples displayed a more significant reductions than the alkali treated samples in the cell wall region. The crystal zone and amorphous zone of cellulose coexisted before and after the treatment, for all of the treated samples, and particularly for the ultrasound-assisted treated samples, the crystallinity increased from 38.15% for water-immersion samples to 57.42% for ultrasound-8% NaOH treated samples.

Effect of particle shape on microstructure and compressive response of 316L SS foam by space holder technique

316 L stainless steel (SS) foams with varying porosities have been developed through PM route using irregular and spherical particles shaped SS powder using urea as space holder. The effect of SS particle shape on microstructure and compressive deformation behaviour of SS foams with varied relative density were studied. The cell size and the cell wall thickness in the foam produced by both types of shapes are comparable. The yield stress, elastic modulus, plateau stress, plastic modulus, micro-hardness and energy absorption values are higher in the foam made through irregular particle shape as compared to spherical one inspite of slightly lesser relative densities. This is due to presence of higher micro-porosities in the cell wall in the foam produced by spherical particles. Therefore, the densification strain is slightly higher in SS foam made with spherical particles. The presence of fewer contacts between spherical powders led to lesser densification in the cell wall region and thus higher micro-porosity evolved. The yield stress, elastic modulus, plateau stress (σpl), plastic modulus and energy absorption (Eab) follow power-law relationship irrespective of SS powder particle shapes. However densification strain follows linear relationship.

How does ultrasound influence the thermal stability of wood?

This study elucidates the mechanism of the influence of ultrasonic treatment on wood pyrolysis and the details of the thermal stability changes of samples treated with ultrasonic alkali are explained. Four groups of samples were designed to clarify this scientific question, including the control group, the ultrasonic water-treated group, the alkali-treated group and the ultrasonic alkali-treated group. The extractives contents (organic extractives and hot water extractives) were determined, the crystal region, the functional groups of chemical components, the distribution of chemical components, and the thermal stability of wood were investigated using X-ray diffraction, Fourier-transform infrared spectroscopy, confocal Raman microscopy, and thermogravimetric analysis, respectively. The results suggested that all the treatments reduced the extractives contents, increased the relative crystallinity, destroyed the structure of hemicellulose and lignin, and affected the thermal stability of wood, to different degrees. Ultrasonic time and alkali concentration were shown to be two important indexes. Ultrasound can enhance the treatment effects of low concentration alkali (0.1 %), but in a highly concentrated alkali environment, the auxiliary effect is not obvious. Ultrasonic treatment reduced the intensity of lignin in the whole cell wall region, while alkali treatment followed a more systematic process as the solvent permeated from the S layer to CCML. The initial degradation temperature T0 was not only related to the extractives content but also to the concentrations of hemicellulose and lignin in the sample. The hemicellulose degradation temperature T1 and cellulose degradation temperature T2 changed with changes in T0. A detailed understanding of the spatial and temporal variations of the major components in the rigid cell wall during the pretreatment process will help to develop more effective pretreatment strategies, which is crucial for the efficient optimization of the process.