Joseph Gril

Effect of circumferential heterogeneity of wood maturation strain, modulus of elasticity and radial growth on the regulation of stem orientation in trees

Active mechanisms of re-orientation are necessary to maintain the verticality of tree stems. They are achieved through the production of reaction wood, associated with circumferential variations of three factors related to cambial activity: maturation strain, longitudinal modulus of elasticity (MOE) and eccentric growth. These factors were measured on 17 mature trees from different botanical families and geographical locations. Various patterns of circumferential variation of these factors were identified. A biomechanical analysis based on beam theory was performed to quantify the individual impact of each factor. The main factor of re-orientation is the circumferential variation of maturation strains. However, this factor alone explains only 57% of the re-orientations. Other factors also have an effect through their interaction with maturation strains. Eccentric growth is generally associated with heterogeneity of maturation strains, and has an important complementary role, by increasing the width of wood with high maturation strain. Without this factor, the efficiency of re-orientations would be reduced by 31% for angiosperms and 26% for gymnosperms. In the case of angiosperms, MOE is often larger in tension wood than in normal wood. Without these variations, the efficiency of re-orientations would be reduced by 13%. In the case of gymnosperm trees, MOE of compression wood is lower than that of normal wood, so that re-orientation efficiency would be increased by 24% without this factor of variations.

Mesoporosity as a new parameter for understanding tension stress generation in trees

The mechanism for tree orientation in angiosperms is based on the production of high tensile stress on the upper side of the inclined axis. In many species, the stress level is strongly related to the presence of a peculiar layer, called the G-layer, in the fibre cell wall. The structure of the G-layer has recently been described as a hydrogel thanks to N(2) adsorption-desorption isotherms of supercritically dried samples showing a high mesoporosity (pores size from 2-50 nm). This led us to revisit the concept of the G-layer that had been, until now, only described from anatomical observation. Adsorption isotherms of both normal wood and tension wood have been measured on six tropical species. Measurements show that mesoporosity is high in tension wood with a typical thick G-layer while it is much less with a thinner G-layer, sometimes no more than normal wood. The mesoporosity of tension wood species without a G-layer is as low as in normal wood. Not depending on the amount of pores, the pore size distribution is always centred around 6-12 nm. These results suggest that, among species producing fibres with a G-layer, large structural differences of the G-layer exist between species.

The effects of adsorbed water on dynamic mechanical properties of wood

Abstract The storage modulus and the loss tangent of Sitka spruce wood ( Picea Sitchensis ) in the longitudinal direction at various moisture contents were measured at 20°C, and the effect of adsorbed water was investigated by using a uniaxial rheological model to eliminate the contribution of matrix swelling. The largest value for Youngs modulus of matrix was obtained at around 8% moisture content. The rearrangement of matrix molecules accompanied by the adsorption of hydrated water increased the value of Youngs modulus up to about 8% moisture content, whereas the plasticization of matrix molecules by the adsorption of dissolved water decreased it at above 8% moisture content. The loss tangent of matrix had two peaks at ∼1% and 20% moisture contents. It was considered that the former was due to the motion of the adsorbed water itself and the latter to the relaxation related to the micro-Brownian motion of matrix substances, especially hemicelluloses.

Characterization of a gel in the cell wall to elucidate the paradoxical shrinkage of tension wood.

Wood behavior is characterized by high sensibility to humidity and strongly anisotropic properties. The drying shrinkage along the fibers, usually small due to the reinforcing action of cellulosic microfibrils, is surprisingly high in the so-called tension wood, produced by trees to respond to strong reorientation requirements. In this study, nitrogen adsorption-desorption isotherms of supercritically dried tension wood and normal wood show that the tension wood cell wall has a gel-like structure characterized by a pore surface more than 30 times higher than that in normal wood. Syneresis of the tension wood gel explains its paradoxical drying shrinkage. This result could help to reduce technological problems during drying. Potential applications in biomechanics and biomimetics are worth investigating, considering that, in living trees, tension wood produces tensile growth stresses 10 times higher than that of normal wood.

A model of anisotropic swelling and shrinking process of wood

Abstract To elucidate the origin of the shrinking anisotropy of wood during the drying process, as well as to begin to gain an understanding of the interaction between the moisture and the cell wall components, the shrinking process of a single wood fiber regarding water desorption was simulated by using an analytical model which was developed in the previous report (Part 1). Resulting data were compared with the experimental ones in this paper. The following conclusions were obtained: (1) The matrix substance, as a skeleton in the secondary wall, tends to shrink isotropically. However, the cellulose microfibrils, as a rigid framework of the cell wall, almost did not shrink at all due to the water desorption. As result, wood shrinks anisotropically during a drying process. The microfibril angle in the S2 layer is one of the most important factors related to the degree of shrinking anisotropy of the wood while drying. (2) According to the simulation, the expansive strain caused in the matrix skeleton by the water sorption increases by 15% (= 150,000 micro-strains) from the oven-dried condition to the green condition. Based on this value, the moisture content at the fiber saturation point is calculated to be about 35%, which is close to the experimentally obtained one. These results give quantitative evidences that the hygroexpansion of the wood cell wall is controlled by the mechanism of the reinforced matrix hypothesis.

GROWTH STRESSES ARE HIGHLY CONTROLLED BY THE AMOUNT OF G-LAYER IN POPLAR TENSION WOOD.

To determine how gelatinous fibres and gelatinous layers contribute to the magnitude of longitudinal growth stress in tension wood, anatomical measurements of gelatinous fibres were carried out on poplar tension wood (Populus I4551). It was found that (a) no gelatinous fibres were observed under a growth strain level of 0.06 to 0.08%; (b) almost 100% of the non-conductive tissues contained gelatinous fibres above a growth strain level of 0.15 to 0.19%; and (c) the area of fibres, the area of fibres with gelatinous layers per unit of tissue area, and the thickness of the gelatinous layers predominantly influenced the magnitude of growth stress

Precautions for the structural analysis of the gelatinous layer in tension wood

The gelatinous layer (G-layer) of tension wood fibres in hardwood contributes to the mechanical function of the living tree and has significant consequences on properties of solid wood. Its size, shape and structure observed by optical or electron microscopy exhibits characteristic anatomical features. However, we found that sectioning of non-embedded wood samples results in an uncontrolled swelling of the G-layer. In order to assess this artefact, the shape and thickness of the G-layer was monitored by serial sections from an embedded wood sample, from its trimmed transverse face to that located several hundreds of micrometres deep. The results revealed that the initial cutting before embedding produced a border effect responsible for the swollen nature, which is similar to sections from non-embedded material. After a conventional embedding technique was applied, a section of at least 30 micrometres below the trimming surface is required to observe an un-swollen G-layer.

Role of the Gelatinous Layer (G-Layer) on the Origin of the Physical Properties of the Tension Wood of Acer sieboldianum

The tension wood (TW) properties of a 70-year-old specimen of Acer sieboldianum Miq. were analyzed by using the G-fiber model that was proposed in our previous report. The roles of the G-layer on the origins of (1) a high tensile growth stress, (2) a large longitudinal Young’s modulus, and (3) a high longitudinal drying shrinkage in the TW xylem are discussed on the basis of the simulations using the G-fiber model. The results suggest that the G-layer generates a high tensile stress in the longitudinal direction during xylem maturation; the longitudinal Young’s modulus of the green G-layer becomes significantly higher than that of the lignified layer; furthermore, the G-layer tends to shrink extraordinarily more than that of the lignified layer during moisture desorption.

Aging of wood: Analysis of color changes during natural aging and heat treatment

Abstract The color properties of aging wood samples from historical buildings have been compared with those of recent wood samples that were heat treated at temperatures ranging from 90°C to 180°C. The results of kinetic analysis obtained by the time-temperature superposition method showed that the color change during natural aging was mainly due to a slow and mild oxidation process. In other words, heat treatment could accelerate the changes in wood color that occur during aging. In one sample, the color change (ΔE* ab ) after 921 years at ambient temperature was almost equivalent to that of heating (artificial aging) approximately for 6.7 h at 180°C. The results have been interpreted that the aging and the subsequent change in wood color begin at the time of tree harvesting.

Colorimetry of wood specimens from French Guiana

The color of 97 species of wood specimens from French Guiana was measured on their radial and tangential surfaces with a colorimeter. We obtained the tristimulus values of X, Y, and Z of the 10° standard observer under the illuminant of D65, and the values of the CIELAB color system, L*, a*, b*, C*, and h. When the lightness index (L*) was <54, b*, C*, and h showed positive correlations against L*. When L* was >54, a* and C* showed negative correlations against L*. These results imply that wood color should be discussed by separating wood specimens into the high and low-lightness groups. A good positive correlation was found between the L* and h throughout the whole range of L*. It is thought that the value of h can be an important index, as can L*, for comparing of wood color because h shows a simple relation with L*.