Jelle Dhaene

Assessment of wood microstructural changes after one-stage thermo-hydro treatment (THT) by micro X-ray computed tomography

Abstract The microstructural changes in a selection of softwoods and hardwoods resulting from thermo-hydro treatment (THT) at 160°C were examined by means of a state-of-the-art micro X-ray computed tomography. A dedicated X-ray scanning and volumetric processing protocol was developed. All reconstructed volumes had an approximate voxel pitch between 0.8 and 1.2 μm3. The microstructures of the same needle-shaped specimens before and after THT were visualized, and the individual parameters (maximum opening and lumen volume) for various cell types were quantified and compared. The highest values of substance volume were recorded for the ash sapwood (81%) and spruce specimens (72%). After THT, a significant correlation was found between the mass loss determined by gravimetry and the X-ray volume loss. The largest change occurred in the lumen volume of several tissue components, such as libriform fibers, tracheids, and ray parenchyma. The average aspen fiber volume reduction after THT was 31%, a value 2.6 times higher than the volume reduction of the average vessels. The porosity of ash sapwood increased from 41 to 56%, whereas the porosity of birch decreased from 34 to 29%.

The effect of craniokinesis on the middle ear of domestic chickens (Gallus gallus domesticus)

The avian middle ear differs from that of mammalians and contains a tympanic membrane, one ossicle (bony columella and cartilaginous extra‐columella), some ligaments and one muscle. The rim of the eardrum (closing the middle ear cavity) is connected to the neurocranium and, by means of a broad ligament, to the otic process of the quadrate. Due to the limited number of components in the avian middle ear, the possibilities of attenuating the conduction of sound seem to be limited to activity of the stapedius muscle. We investigate to what extent craniokinesis may impact the components of the middle ear because of the connection of the eardrum to the movable quadrate. The quadrate is a part of the beak suspension and plays an important role in craniokinesis. Micro‐computed tomography was used to visualize morphology and the effect of craniokinesis on the middle ear in the domestic chicken (Gallus gallus domesticus). Both hens and roosters are considered because of their difference in vocalization capacity. It is hypothesized that effects, if present, of craniokinesis on the middle ear will be greater in roosters because of their louder vocalization. Maximal lower jaw depression was comparable for hens and roosters (respectively 34.1 ± 2.6° and 32.7 ± 2.5°). There is no overlap in ranges of maximal upper jaw elevation between the sexes (respectively 12.7 ± 2.5° and 18.5 ± 3.8°). Frontal rotation about the transversal quadrato‐squamosal, and inward rotation about the squamosal‐mandibular axes of the quadrate were both considered to be greater in roosters (respectively 15.4 ± 2.8° and 11.1 ± 2.5°). These quadrate rotations did not affect the columellar position or orientation. In hens, an influence of the quadrate movements on the shape of the eardrum could not be detected either; however, craniokinesis caused slight stretching of the eardrum towards the caudal rim of the otic process of the quadrate. In roosters, an inward displacement of the conical tip of the tympanic membrane of 0.378 ± 0.21 mm, as a result of craniokinesis, was observed. This is linked to a flattening and slackening of the eardrum. These changes most likely go along with a deformation of the extra‐columella. Generally, in birds, larger beak opening is related to the intensity of vocalization. The coupling between larger maximal upper jaw lifting in roosters and the slackening of the eardrum suggest the presence of a passive sound attenuation mechanism during self‐vocalization.

Investigating the interaction between internal structural changes and water sorption of MDF and OSB using X-ray computed tomography

Both medium density fiberboard (MDF) and oriented strand board (OSB) are increasingly used in construction, yet when exposed, water sorption can cause internal structural changes, as such decreasing mechanical strength and increasing decay risk. It is, therefore, essential to understand the interaction between structural changes and water sorption of MDF and OSB. Detailed water sorption behavior and related structural changes in two types of MDF and two types of OSB were periodically monitored using a gantry-based X-ray CT scanner. Water sorption causes local swelling in MDF, resulting in reduced swelling or even shrinkage in neighboring regions. Then again, local shrinkage can increase water resistance and possibly decrease water content locally. Obviously, local swelling results in structural changes. Such structural changes predominantly seem to appear in the transition area between high and low porosity regions. Structural changes, such as glue bonding detachment and cracking, could facilitate water intake in both MDF and OSB. For the studied T-MDF and OSB-A, the relative position of wood fibers/strands and the volume of the voids hardly changed during water sorption, which probably contributes to the decrease in water sorption along newly formed cracks and voids induced by structural changes.

Built to bite? Differences in cranial morphology and bite performance between narrow‐ and broad‐headed European glass eels

The presence of two phenotypes in a single species is a widespread phenomenon, also observed in European eel (Anguilla anguilla). This dimorphism has been related to dietary differences in the subadult elver and yellow eel stages, with broad‐heads generally feeding on harder and/or larger‐bodied prey items than narrow‐heads. Nevertheless, both broad‐ and narrow‐headed phenotypes can already be found among glass eels, the stage preceding the elver eel stage. As these glass eels are considered nonfeeding, we investigate here to what degree the observed variation in head width is reflected in variation in the musculoskeletal feeding system, as well as whether this reflects the same variation observed in the older, dimorphic yellow eels. Additionally, we investigate whether musculoskeletal differences between broad‐ and narrow‐headed glass eels have implications on their feeding performance and could thus impact prey preference when eels start feeding. Therefore, we compared the cranial musculoskeletal system of five broad‐ and narrow‐headed glass eels using 3D‐reconstructions and simulated the glass eels bite force using the data of the muscle reconstructions. We found that the variation in the musculoskeletal system of glass eels indeed reflects that of the yellow eels. Broader heads were related to larger jaw muscles, responsible for mouth closure. Accordingly, broad‐heads could generate higher bite forces than narrow‐headed glass eels. In addition, broader heads were associated with higher coronoid processes and shorter hyomandibulae, beneficial for dealing with higher mechanical loadings and consequently, harder prey. We, thus, show that head width variation in glass eels is related to musculoskeletal differences which, in turn, can affect feeding performance. As such, differences in prey preference can already take place the moment the eels start feeding, potentially leading to the dimorphism observed in the elver and yellow eel stage.

Cranial vault thickness variation and inner structural organization in the StW 578 hominin cranium from Jacovec Cavern, South Africa

The Sterkfontein Caves site is one of the richest early hominin fossil localities in Africa. More specifically, the fossiliferous deposits within the lower-lying Jacovec Cavern have yielded valuable hominin remains; prominent among them is the Australopithecus partial cranium StW 578. Due to the fragmentary nature of the braincase, the specimen has not yet been formally assigned to a species. In this context, we employ microtomography to quantify cranial thickness and composition of StW 578 in order to assess its taxonomic affinity. As comparative material, we investigate 10 South African hominin cranial specimens from Sterkfontein (StW 505, Sts 5, Sts 25, Sts 71), Swartkrans (SK 46, SK 48, SK 49) and Makapansgat (MLD 1, MLD 10, MLD 37/38), attributed to either Australopithecus or Paranthropus, as well as 10 extant human and 10 extant chimpanzee crania. Thickness variation in and structural arrangement of the inner and outer cortical tables and the diploë are automatically assessed at regular intervals along one parasagittal and one coronal section. Additionally, topographic cranial vault thickness distribution is visualized using color maps. Comparisons highlight an absolutely and relatively thickened condition of the StW 578 cranial vault versus those of other South African Plio-Pleistocene hominins. Moreover, in StW 578, as well as in the Australopithecus specimens Sts 5 and Sts 71 from Sterkfontein, the diploic layer contributes substantially to cumulative vault thickness (i.e., >60%). Within the comparative sample investigated here, StW 505 and Sts 71 from Sterkfontein Member 4, both attributed to Australopithecus, most closely resemble StW 578 in terms of cranial vault thickness values, tissue proportions, and two- and three-dimensional distributions. Including additional Plio-Pleistocene Australopithecus and Paranthropus crania from South and East Africa in future studies would further help establish morphological variability in these hominin taxa.

Dimorphism throughout the European eel's life cycle: are ontogenetic changes in head shape related to dietary differences?

A well‐known link exists between an organisms ecology and morphology. In the European eel, a dimorphic head has been linked to differences in feeding ecology, with broad‐headed eels consuming harder prey items than narrow‐headed ones. Consequently, we hypothesized that broad‐heads should exhibit a cranial musculoskeletal system that increases bite force and facilitates the consumption of harder prey. Using 3D‐reconstructions and a bite model, we tested this hypothesis in two life stages: the sub‐adult yellow eel stage and its predecessor, the elver eel stage. This allowed us to test whether broad‐ and narrow‐headed phenotypes show similar trait differences in both life stages and whether the dimorphism becomes more pronounced during ontogeny. We show that broad‐headed eels in both stages have larger jaw muscles and a taller coronoid, which are associated with higher bite forces. This increased bite force together with the elongated upper and lower jaws in broad‐headed eels can also improve grip during spinning behavior, which is used to manipulate hard prey. Head shape variation in European eel is therefore associated with musculoskeletal variation that can be linked to feeding ecology. However, although differences in muscle volume become more pronounced during ontogeny, this was not the case for skeletal features.

Investigating plywood behaviour in outdoor conditions

Moisture behaviour of plywood is investigated in combination with detailed structural analysis. In the lab, neutron radiography and X-ray computed tomography (X-ray CT) were used to map the moisture distribution and internal structure of plywood respectively. In an outdoor natural weathering test, the average moisture content (MC) and moisture distribution of plywood were monitored using a continuous moisture measurement set-up and an adapted electrical method, respectively. The structural changes of the specimens during weathering were recorded by using X-ray CT. Based on the interrelationship of moisture behaviour and structure, suggestions are given for improving the water resistance of plywood by optimising structure.