Cross sections of a 203‐mm diam. soil core taken from a site under Kentucky bluegrass (Poa pratensis L.) were scanned using x‐ray computed tomography (CT) to determine if macropores such as cracks, earthworm holes and root channels could be distinguished and characterized. The core was physically sectioned at the same locations as the CT scans to verify the size and location of pores seen on the CT images. Macropores 1 mm and larger could be easily and quickly distinguished by the method. By manipulation of the scanner images, air‐filled pores, roots and stones were identified within the soil matrix. A wet bulk density plus an air‐filled macroporosity were calculated for scans. Prior to sectioning, a dye solution was ponded on the surface of the core and allowed to infiltrate to assess the continuity of pores through the core.
Accurately determining the dose from low energy x rays is becoming increasingly important. This is especially so because of high doses in interventional radiology procedures and also because of the desire to model accurately the dose around low energy brachytherapy sources. Various methods to estimate the dose from specific procedures are available but they only give a general idea of the true dose to various organs. The use of sophisticated three-dimensional (3D) dose deposition algorithms designed originally for radiation therapy treatment planning can be extended to lower photon energy regions. The majority of modern 3D treatment planning systems use a variation of the convolution algorithm to calculate dose distributions. This could be extended into the diagnostic energy range with the availability of lower energy deposition kernels ( < 100 keV). We have used version four of the Electron Gamma Shower (EGS4) system of Monte Carlo codes to generate photon energy deposition kernels in the energy range of 20-110 keV and have implemented them in a commercial 3D treatment planning system (Pinnacle, ADAC Laboratories, Milpitas, CA). The kernels were generated using the "SCASPH" EGS4 user code by selecting the appropriate transport parameters suitable for the relative low energy of the incident photons. The planning system was subsequently used to model diagnostic quality beams and to calculate depth dose and cross profile curves. Comparisons of the calculated curves have been made with measurements performed in a homogeneous water phantom.
A phantom composed of 30% glandular tissue and 70% adipose tissue allows closer simulation of the phototimer response of the mammographic x-ray unit for the average breast. The phantom currently used contains 16% more glandular tissue than the average breast.
Several problems related to the true value of quantitative information from CT scanners in improving estimates of photon-beam isodose distribution remain unanswered. The authors conclude that two widely used correction factors provide satisfactory isodose corrections behind heterogeneities of simple geometry. Lateral perturbations were found to be small for megavoltage photon beams, indicating that complex computational schemes are uncalled for. It appears doubtful that the use of CT information in megavoltage photon-beam isodose curve generation requires (a) larger computers than those currently available either in existing therapy planning systems or on the scanner itself or (b) direct access to the CT numbers.
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