Abstract: Wood maturation strains can be estimated from the change in curvature that occurs when a stem grown staked in tilted position is released from the stake.
Trees have a motor system to enable upright growth in the field of gravity. This motor function is taken on by reaction wood, a special kind of wood that typically develops in leaning axes and generates mechanical force during its formation, curving up the stem and counteracting the effect of gravity or other mechanical disturbances. Quantifying the mechanical stress induced in wood during maturation is essential to many areas of research ranging from tree architecture to functional genomics. Here, we present a new method for quantifying wood maturation stress. It consists of tilting a tree, tying it to a stake, letting it grow in tilted position, and recording the change in stem curvature that occurs when the stem is released from the stake. A mechanical model is developed to make explicit the link between the change in curvature, maturation strain and morphological traits of the stem section. A parametric study is conducted to analyse how different parameters influence the change in curvature. This method is applied to the estimation of maturation strain in two different datasets. Results show that the method is able to detect genotypic variations in motor power expression. As predicted by the model, we observe that the change in stem curvature is correlated to stem diameter and diameter growth. In contrast, wood maturation strain is independent from these dimensional effects, and is suitable as an intrinsic parameter characterising the magnitude of the plant’s gravitropic reaction.

Abstract: Trees can modify their wood structure in response to changes in mechanical, hydraulic and storage demands during their life-cycles. Thus, examining radial variations in wood traits is important to expand our knowledge of tree functioning and species ecological strategies. Yet, several aspects of radial changes in wood functional traits are still poorly understood, especially in angiosperm trees from tropical humid forests. Here, we examined radial shifts in wood traits in trunks of tropical forest species and explored their potential ecological implications. We first examined radial variations in wood specific gravity (WSG). Then, we asked what anatomical traits drove radial variations in WSG, and whether WSG, vessel fraction and specific hydraulic conductivity vary independently from each other along the radius gradients. We measured WSG and eight wood anatomical traits, at different radial positions along the trunks, in 19 tree species with contrasting shade-tolerance from a lowland tropical forest in eastern Amazonia. Most species had significant radials shifts in WSG. Positive radial gradients in WSG (i.e., increments from pith to bark) were common among shade-intolerant species and were explained by different combinations of fiber and parenchyma traits, while negative radial shifts in WSG (e.g., decreases towards the bark) were present in shade-tolerants, but were generally weakly related to anatomical traits. We also found that, in general, WSG was unrelated to vessel fraction and specific hydraulic conductivity in any radial position. This study illustrates the contrasting radial variations in wood functional traits that occur in tree species from a humid lowland tropical forest. In particular, our results provide valuable insights into the anatomical traits driving WSG variations during tree development. These insights are important to expand our knowledge on tree ecological strategies by providing evidence on how wood allocation varies as trees grow, which in turn can be useful in studying trait-demography associations, and in estimating tree above-ground biomass.

Abstract: Plant tissues shrink and swell in response to changes in water pressure. These strains can be easily measured, e.g., at the surface of tree stems, to obtain indirect information about plant water status and other physiological parameters. We developed a mechanical model to clarify how water pressure is transmitted to cell walls and causes shrinkage of plant tissues, particularly in the case of thick-walled cells such as wood fibers. Our analysis shows that the stress inside the fiber cell walls is lower than the water tension. The difference is accounted for by a stress transmission factor that depends on two main effects. The first effect is the dilution of the stress through the cell wall, because water acts at the lumen border and is transmitted to the cuter border of the cell, which has a larger circumference. The second effect is the partial conversion of radial stress into tangential stress. Both effects are quantified as functions of parameters of the cell wall structure and its mechanical properties.

Abstract: The relationship between maintenance respiration (R.) of woody organs and their structural characteristics was explored in adult Pinus pinaster Ait. trees. We measured R-m on 75 stem and branch segments of different ages (from 3 to 24 years) and diameters (from 1 to 35 cm). The temperature response of R-m was derived from field measurements based on a classical exponential function with Q(10) = 2.13. Relationships between R-m and the dimensions of the woody organs were analyzed under controlled conditions in the laboratory. The surface area of a woody organ was a better predictor of R-m than volume, but surface area failed to account for the observed within-tree variability of R-m among stems, branches and twigs. Two simple models were proposed to predict the variability of R-m at 15 degreesC in an adult tree. Model 1, a linear function model based on the dry mass and nitrogen concentration of sapwood and phloem tissues, explained most of the variability of R-m in branches and stems (R-2 = 0.97). We concluded that the respective contributions of the phloem and sapwood depend on the location and diameter of the woody organ. Model 2, a power-law function model based on the length, diameter and age of the sample, explained the same variance of R-m as Model 1 and is appropriate for scaling R-m to the stand level. Models 1 and 2 appear to explain a larger variability of R-m than models based on stem area or sapwood mass.

Abstract: To recover verticality after disturbance, angiosperm trees produce 'tension wood' allowing them to bend actively. The driving force of the tension has been shown to take place in the G-layer, a specific unlignified layer of the cell wall observed in most temperate species. However, in tropical rain forests, the G-layer is often absent and the mechanism generating the forces to reorient trees remains unclear. A study was carried out on tilted seedlings, saplings and adult Simarouba amara Aubl. trees – a species known to not produce a G-layer. Microscopic observations were done on sections of normal and tension wood after staining or observed under UV light to assess the presence/absence of lignin. We showed that S. amara produces a cell-wall layer with all of the characteristics typical of G-layers, but that this G-layer can be observed only as a temporary stage of the cell-wall development because it is masked by a late lignification. Being thin and lignified, tension wood fibres cannot be distinguished from normal wood fibres in the mature wood of adult trees. These observations indicate that the mechanism generating the high tensile stress in tension wood is likely to be the same as that in species with a typical G-layer and also in species where the G-layer cannot be observed in mature cells. © 2015 The Author 2015. Published by Oxford University Press. All rights reserved.