Separation of soil macropore types in three-dimensional X-ray computed tomography images based on pore geometry characteristics

In structured soils, earthworm burrows, root channels, shrinkage cracks, and interaggregate spaces form complex macropore networks. Depending on the type and morphological properties, each macropore surface type is coated with specific organo-mineral compounds, differently affecting sorption and mass exchange during preferential flow and turnover processes. For a quantitative, macropore type-specific analysis using X-ray computed tomography (XRCT) with subsequent three-dimensional (3D) image analysis, a discrimination of biopores from cracks and interaggregate spaces is necessary. We developed a method that allows separating biopores from other larger macropores in 3D images from XRCT of intact soil cores. An image-processing workflow using the MAVI (Modular Algorithms for Volume Images) software framework ToolIP (Tool for Image Processing) was created to handle XRCT 3D images. Masking steps enabled to retain the surface roughness in the resulting two images of separated biopores and cracks. As a key point, the sizes of the structuring elements used in the spherical opening and dilation were objectively determined. For this purpose, maximum differences in the pore shapes between the 3D images of cylindrical biopores vs. more flat cracks and unregularly interaggregate spaces were focused. At the given resolution of 231-mm voxel edge length, an optimum size of 2.5 voxels was found for both processing steps. The voxel-based approach is applicable to XRCT 3D images of different spatial resolution and appears useful for the quantification of physicochemical surface properties of different macropore types for soil volumes, enabling a more precise description of preferential flow and transport

Repetitive recombinant human bone morphogenetic protein 2 injections improve the callus microarchitecture and mechanical stiffness in a sheep model of distraction osteogenesis

Evidence suggests that recombinant human bone morphogenetic protein 2 (rhBMP-2) increases the mechanical integrity of callus tissue during bone healing. This effect may be either explained by an increase of callus formation or a modification of the trabecular microarchitecture. Therefore the purpose of the study was to evaluate the potential benefit of rhBMP-2 on the trabecular microarchitecture and on multidirectional callus stiffness. Further we asked, whether microarchitecture changes correlate with optimized callus stiffness. In this study a tibial distraction osteogenesis (DO) model in 12 sheep was used to determine, whether percutaneous injection of rhBMP-2 into the distraction zone influences the microarchitecture of the bone regenerate. After a latency period of 4 days, the tibiae were distracted at a rate of 1.25 mm/day over a period of 20 days, resulting in total lengthening of 25 mm. The operated limbs were randomly assigned to one treatment groups and one control group: (A) triple injection of rhBMP-2 (4 mg rhBMP-2/injection) and (B) no injection. The tibiae were harvested after 74 days and scanned by µCT (90 µm/voxel). In addition, we conducted a multidirectional mechanical testing of the tibiae by using a material testing system to assess the multidirectional strength. The distraction zones were tested for torsional stiffness and bending stiffness antero-posterior (AP) and medio-lateral (ML) direction, compression strength and maximum axial torsion. Statistical analysis was performed using multivariate analysis of variance (ANOVA) followed by student's t-test and Regression analysis using power functions with a significance level of P<0.05. Triple injections of rhBMP-2 induced significant changes in the trabecular architecture of the regenerate compared with the control: increased trabecular number (Tb.N.) (treatment group 1.73 mm/1 vs. control group 1.2 mm/1), increased cortical bone volume fraction (BV/TV) (treatment group 0.68 vs. control group 0.47), and decreased trabecular separation (Tb.Sp.) (treatment group 0.18 mm vs. control group 0.43 mm)

ERRATUM: Repetitive recombinant human bone morphogenetic protein 2 injections improve the callus microarchitecture and mechanical stiffness in a sheep model of distraction osteogenesis

Due to a technical error, Dr. Marc-Frederic Pastor was omitted from the author list of this article. The correct author details appear above.<br /