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Reaction wood is a wood defect arising during the growth of the tree in the part of the trunk that is under tension (hardwood tree species) or compression (coniferous tree species). Beech (Fagus sylvatica L.) tension wood has different anatomical and chemical characteristics than normal (opposite) wood. The difference in density is conditioned by the percentage of the gelatinous layer (G-layer). Fibre cells in reaction beech wood have a different cell wall structure and a different chemical composition. Tension wood cannot be detected by the naked eye. It is only possible to assume its occurrence based on the macroscopic characteristics of the logs, such as a woolly surface, taper or eccentric pith, and so forth. However, these are imprecise and unreliable methods that have minimal effectiveness, especially when shortening the length of the log for cut-outs. This study aimed to create a unique chemical reagent for the detection of tension wood in logs and timber and wood products immediately. The present research can contribute to the mitigation of flaws resulting from the reaction of wood in timber production while addressing noticeable constraints in manufacturing, such as energy resources and the availability of wood raw materials. This can be achieved through the efficient identification of reaction wood in materials. The colour change is only temporary and will fade over time. After the chemical reagent has dried on the surface, the surface can be milled. The colour change extends to a depth of approx. of 3 to 5 mm.

Reaction wood is a wood defect arising during the growth of the tree in the part of the trunk that is under tension (hardwood tree species) or compression (coniferous tree species). Beech (Fagus sylvatica L.) tension wood has different anatomical and chemical characteristics than normal (opposite) wood. The difference in density is conditioned by the percentage of the gelatinous layer (G-layer). Fibre cells in reaction beech wood have a different cell wall structure and a different chemical composition. Tension wood cannot be detected by the naked eye. It is only possible to assume its occurrence based on the macroscopic characteristics of the logs, such as a woolly surface, taper or eccentric pith, and so forth. However, these are imprecise and unreliable methods that have minimal effectiveness, especially when shortening the length of the log for cut-outs. This study aimed to create a unique chemical reagent for the detection of tension wood in logs and timber and wood products immediately. The present research can contribute to the mitigation of flaws resulting from the reaction of wood in timber production while addressing noticeable constraints in manufacturing, such as energy resources and the availability of wood raw materials. This can be achieved through the efficient identification of reaction wood in materials. The colour change is only temporary and will fade over time. After the chemical reagent has dried on the surface, the surface can be milled. The colour change extends to a depth of approx. of 3 to 5 mm.

Reaction wood is characterized by having different anatomical and chemical features than normal wood. The different composition of cell walls, the higher quantitative proportion of thick-wall fiber cells, diameter, and the abundance of vessels have remarkable effects on reaction wood’s physical and mechanical properties. Reaction wood has fewer vascular cells. In addition, it has a smaller lumen diameter, which results in reduced permeability. Therefore, reaction wood is more difficult to dry at a certain moisture content. The differences in the drying times of the reaction wood and the normal wood were largest at a temperature of 60 °C and durations greater than 30 h, and the reaction wood dried more slowly. At a temperature of 120 °C, the differences in drying time were minimalized, and drying end times were almost identical. The expected negative effect of higher temperature on the morphology of reaction wood and opposition wood was not confirmed.

Background and AimsAngiosperm trees generally form tension wood on the upper sides of leaning stems. The formation of tension wood is an important response to gravitational stimulus. Gibberellin appears to be involved in the differentiation of secondary xylem, but it remains unclear whether gibberellin plays a key role in the formation of tension wood and plant gravitropism. Therefore, a study was designed to investigate the effects of gibberellin and of inhibitors of the synthesis of gibberellin, namely paclobutrazole and uniconazole-P, on the formation of tension wood and negative stem gravitropism in Acacia mangium seedlings.MethodsGibberellic acid (GA3), paclobutrazole and uniconazole-P were applied to seedlings via the soil in which they were growing. Distilled water was applied similarly as a control. Three days after such treatment, seedlings were tilted at an angle of 45° from the vertical, and samples of stems were collected for analysis 2 weeks, 2 months and 6 months after tilting. The effects of treatments on the stem recovery degree (Rº) were analysed as an index of the negative gravitropism of seedlings, together the width of the region of tension wood in the upper part of inclined stems.Key ResultsIt was found that GA3 stimulated the negative gravitropism of tilted seedling stems of A. mangium, while paclobutrazole and uniconazole-P inhibited recovery to vertical growth. Moreover, GA3 stimulated the formation of tension wood in tilted A. mangium seedlings, while paclobutrazole and uniconazole-P strongly suppressed the formation of tension wood, as assessed 2 weeks after tilting.ConclusionsThe results suggest that gibberellin plays an important role at the initial stages of formation of tension wood and in stem gravitropism in A. mangium seedlings in response to a gravitational stimulus.

The paper is focused on the comparison of selected properties of the tension and normal wood. Beech is wood with high frequency of defects such as red false heartwood, reaction wood (tension wood), dote and so forth. The quality of beech wood is determined according to the structure and properties. The tension wood is considered an important wood defect because it causes negative alterations in solid wood quality and limits an industrial utilization of the wood. Tension wood content in our research was evaluated by the initial longitudinal warping and the woolly appearance of surface. The wood turning blanks of normal and tension wood were selected with a thickness of approximately 50 mm, width of 55 mm, and length of 460 mm. Quantity of 32 woodturning blanks were determined for moisture content and 16 samples for density from two groups tension [TW] and normal wood [NW]. Fourier transform-infrared (FTIR) spectroscopy measurements were carried out using a Nicolet iS10 FTIR spectrometer equipped with Smart iTR attenuated total reflectance (ATR) sampling accessory with diamond crystal (Thermo Fisher Scientific). A resolution of 4 cm-1 and 32 scans per sample was used. Higher variations in average moisture content were in the samples of tension. No significant statistical differences were found between density of tension and normal wood samples measured in fresh state. The cellulose in tension wood has higher degree of crystallinity than in normal wood.

Bioenergy will be one of the most important renewable energy sources in the conversion from fossil fuels to bio‐based products. Short rotation coppice Salix could be a key player in this conversion since Salix has rapid growth, positive energy balance, easy to manage cultivation system with vegetative propagation of plant material and multiple harvests from the same plantation. The aim of the present paper is to provide an overview of the main challenges and key issues in willow genetic improvement toward sustainable biofuel value chains. Primarily based on results from the research project “Optimized Utilization of Salix” (OPTUS), the influence of Salix wood quality on the potential for biofuel use is discussed, followed by issues related to the conversion of Salix biomass into liquid and gaseous transportation fuels. Thereafter, the studies address genotypic influence on soil carbon sequestration in Salix plantations, as well as on soil carbon dynamics and climate change impacts. Finally, the opportunities for plant breeding are discussed using willow as a resource for sustainable biofuel production. Substantial phenotypic and genotypic variation was reported for different wood quality traits important in biological (i.e., enzymatic and anaerobic) and thermochemical conversion processes, which is a prerequisite for plant breeding. Furthermore, different Salix genotypes can affect soil carbon sequestration variably, and life cycle assessment illustrates that these differences can result in different climate mitigation potential depending on genotype. Thus, the potential of Salix plantations for sustainable biomass production and its conversion into biofuels is shown. Large genetic variation in various wood and biomass traits, important for different conversion processes and carbon sequestration, provides opportunities to enhance the sustainability of the production system via plant breeding. This includes new breeding targets in addition to traditional targets for high yield to improve biomass quality and carbon sequestration potential. Bioenergy will be one of the most important renewable energy sources in the conversion from fossil fuels to bio‐based products. Short‐rotation‐coppice Salix could be a key player in this conversion since Salix has rapid growth, positive energy balance, an easy to manage cultivation system with vegetative propagation of plant material and multiple harvests from the same plantation. The paper provides an overview of the main challenges and key issues in willow genetic improvement towards sustainable biofuel value chains.

Background Interest on the use of short rotation willow as a lignocellulose resource for liquid transport fuels has increased greatly over the last 10 years. Investigations have shown the advantages and potential of using Salix spp. for such fuels but have also emphasized the wide variations existing in the compositional structure between different species and genotypes in addition to their effects on overall yield. The present work studied the importance of tension wood (TW) as a readily available source of glucose in 2-year-old stems of four Salix clones (Tora, Björn, Jorr, Loden). Studies involved application of a novel approach whereby TW-glucose and residual sugars and lignin were quantified using stem cross sections with results correlated with HPLC analyses of milled wood. Compositional analyses were made for four points along stems and glucose derived from enzyme saccharification of TW gelatinous (G) layers (G-glucose), structural cell wall glucose (CW-glucose) remaining after saccharification and total glucose (T-glucose) determined both theoretically and from HPLC analyses. Comparisons were also made between presence of other characteristic sugars as well as acid-soluble and -insoluble lignin. Results Preliminary studies showed good agreement between using stem serial sections and milled powder from Salix stems for determining total sugar and lignin. Therefore, sections were used throughout the work. HPLC determination of T-glucose in Salix clones varied between 47.1 and 52.8%, showing a trend for higher T-glucose with increasing height (Björn, Tora and Jorr). Using histochemical/microscopy and image analysis, Tora (24.2%) and Björn (28.2%) showed greater volumes of % TW than Jorr (15.5%) and Loden (14.0%). Total G-glucose with enzyme saccharification of TW G-layers varied between 3.7 and 14.7% increasing as the total TW volume increased. CW-glucose measured after enzyme saccharification showed mean values of 41.9–49.1%. Total lignin between and within clones showed small differences with mean variations of 22.4–22.8% before and 22.4–24.3% after enzyme saccharification. Calculated theoretical and quantified values for CW-glucose at different heights for clones were similar with strong correlation: T-glucose = G-glucose + CW-glucose. Pearson’s correlation displayed a strong and positive correlation between T-glucose and G-glucose, % TW and stem height, and between G-glucose with % TW and stem height. Conclusions The use of stem cross sections to estimate TW together with enzyme saccharification represents a viable approach for determining freely available G-glucose from TW allowing comparisons between Salix clones. Using stem sections provides for discrete morphological/compositional tissue comparisons between clones with results consistent with traditional wet chemical analysis approaches where entire stems are milled and analyzed. The four clones showed variable TW and presence of total % G-glucose in the order Björn > Tora > Jorr > Loden. Calculated in terms of 1 m 3 , Salix stems Tora and Björn would contain ca. 0.24 and 0.28 m 3 of tension wood representing a significant amount of freely available glucose. Graphical Abstract

After gibberellin had been applied to the vertical stems of four species of angiosperm trees for approximately 2 months, we observed eccentric radial growth that was due to the enhanced growth rings on the sides of stems to which gibberellin had been applied. Moreover, the application of gibberellin resulted in the formation of wood fibers in which the thickness of inner layers of cell walls was enhanced. These thickened inner layers of cell walls were unlignified or only slightly lignified. In addition, cellulose microfibrils on the innermost surface of these thickened inner layers of cell walls were oriented parallel or nearly parallel to the longitudinal axis of the fibers. Such thickened inner layers of cell walls had features similar to those of gelatinous layers in the wood fibers of tension wood, which are referred to as gelatinous fibers. Our anatomical and histochemical investigations indicate that the application of gibberellin can induce the formation of tension wood on vertical stems of angiosperm trees in the absence of gravitational stimulus.

Tension wood formed in response to gravitational force is a striking example of the plasticity of angiosperm wood. In this study our goal was to characterize the early changes in gene expression during tension wood formation in Eucalyptus.Using cDNA array technology, transcript profiling of 231 genes preferentially expressed in differentiating Eucalyptus xylem was followed from 6 h to 1 wk of a tension time course of artificially bent Eucalyptus trees.196 genes were differentially regulated between control and bent trees, some exhibiting distinctive expression patterns related to changes in secondary cell wall structure and composition. For instance, expression of a cellulose synthase gene was well correlated with the appearance of the G-layers. Cluster correlation analysis revealed differential regulation of lignin biosynthetic genes and may also be used to help infer the function of unknown gene products.Eucalyptus wood transcriptome analysis during tension wood formation not only provided new clues into the transcriptional regulatory network of genes preferentially expressed in xylem, but also highlighted candidate genes responsible for the genetic and environmentally induced variation of wood quality traits.

• Brassinosteroids have been implicated in the differentiation of vascular cell types in herbaceous plants, but their roles during secondary growth and wood formation are not well defined. • Here we pharmacologically and genetically manipulated brassinosteroid levels in poplar trees and assayed the effects on secondary growth and wood formation, and on gene expression within stems. • Elevated brassinosteroid levels resulted in increases in secondary growth and tension wood formation, while inhibition of brassinosteroid synthesis resulted in decreased growth and secondary vascular differentiation. Analysis of gene expression showed that brassinosteroid action is positively associated with genes involved in cell differentiation and cell-wall biosynthesis. • The results presented here show that brassinosteroids play a foundational role in the regulation of secondary growth and wood formation, in part through the regulation of cell differentiation and secondary cell wall biosynthesis.