Hydraulic contacts controlling water flow across porous grains.

Water flow between porous grains varies widely depending on the water distribution in contacts between grains. The hydraulic behavior of contacts varies from highly conductive when water fills the contacts to a bottleneck to flow as water pressure drops and contact asperities rapidly drain. Such changes greatly impact the hydraulic conductivity of porous grain packs such as aggregated soil. The dominant driving force of water flow across contacts is capillarity, often quantified relative to gravity and viscous forces using the capillary and Bond numbers. For fast water infiltration, viscous forces dominate. For simplicity we modeled the water distribution between spherical porous grains whose surfaces are covered by spherical bumps of much smaller radii. We provide experimental evidence obtained by neutron radiography and synchrotron-based x-ray tomographic microscopy documenting transitions in the flow behavior across contacts.

Time-dependent distribution of surface-applied radionuclides and their recovery in maize during the growing season.

The spatial and temporal heterogeneity of field soils influences the fate and behavior of strongly sorbing pollutants and their entry into the food chain. We studied the redistribution of surface-applied 54Mn, 65Zn, 57Co, and 134Cs in the soil profile and their recovery in the aerial parts of maize grown on an untilled agricultural soil during the growing season. Radionuclides were more concentrated in the preferential flow paths (PFP) than in the soil matrix and their concentration decreased with time. The recovery of 54Mn in the aerial plant parts increased between pollen shed and maturity, while the recovery of 65Zn and 57Co did not show any significant difference, and the recovery of 134Cs decreased with time. The amount and distribution of rainfall, and the chemical, physical, and microbiological soil characteristics are the major factors influencing the variation of radionuclide recovery with time.

Is the transfer factor a relevant tool to assess the soil-to-plant transfer of radionuclides under field conditions?

The radiological impact of radionuclides released to the terrestrial environment is usually predicted with mathematical models in which the transfer of radionuclides from soil to the plant is described with the transfer factor (TF). This paper questions the validity of the protocols proposed by the International Atomic Energy Agency to measure TF in the field and in greenhouses conditions. We grew maize (Zea mays L.) both in the field after a surface application of radionuclides ((54)Mn, (57)Co, (65)Zn, and (134)Cs) and in a greenhouse with the same soil that has received the same fertilization and that had been previously sieved and homogeneously labeled with the same radionuclides before being repacked in pots. The analysis of the displacement of radionuclides in the field soil profile showed a higher concentration of the surface-applied radionuclides in the preferential flow path (PFP) in comparison to the soil matrix indicating that they infiltrated heterogeneously in the soil profile due to the structure-induced non-uniform water flow. A significantly higher recovery of (57)Co and (134)Cs was observed in the plants grown in the field soil, whereas no differences in the recovery of (54)Mn and (65)Zn between the two experiments were detected. These results suggest that (i) under field conditions the soil-to-plant transfer of radionuclides that co-exist as stable elements present at low concentrations in the soil and in the plant is higher than that measured under greenhouse conditions and (ii) the implicit assumption made when calculating the TF (that radionuclides are homogeneously distributed in the soil profile) is not valid, thereby preventing the calculation of an average concentration to obtain the TF parameter.

Behavior of a surface applied radionuclide and a dye tracer in structured and repacked soil monoliths.

There has been increasing evidence in recent years about the impact of soil structure on vadose zone hydrology and the distribution of surface applied chemical substances. We have carried out a combined dye and radionuclide tracer study on two monoliths from the same location, one structured and one repacked, as part of an ongoing study to investigate the link between preferential flow, leaching of surface applied substances and their distribution within the soil.A tracer solution containing 1300 Bq/L (58)Co and 0.31 micromol/L Sulforhodamine B (SB) was added with roughly constant irrigation during a period of three weeks. The dye served as a tracer for water movement within the soil and thus allowed linkage of the radiotracer ((58)Co) with the flow pattern. Both were monitored in the outflow and measured within profile sections after monolith disassembly. Preferential flow in the structured monolith promoted the bypass and transport of both tracers, although transport was impeded at depths greater than 30 cm by compacted soil and reduced hydraulic conductivity. Eighty four percent of radiocobalt and 8% of SB were found in the upper 4 cm of the structured monolith. The homogenized monolith, on the other hand, showed mostly chromatographic infiltration and a more efficient soil filtering capacity with 91% of radiocobalt and 20% SB residing in the upper 4 cm. Furthermore no tracer was found in the outflow of the homogenized monolith during normal to high irrigation or at greater depth within the monolith. We have related flow characteristics and sorption of radiotracers by quantifying dye distributions and radionuclide activities throughout the profiles. Activities within the flow paths are up to 20-times higher than those measured in the soil matrix, and a fraction of radiocobalt follows the dye tracer in spite of cobalt's low mobility. The dye can thus be used to trace radionuclide distribution within the soil block.

Fluorescence imaging of tracer distributions in soil profiles.

To evaluate and parametrize transport models for the vadose (partially water-unsaturated) zone, information about the spatial distributions of solutes is needed. We describe a technique for the simultaneous imaging of several fluorescent tracers in structured field soils. With this technique, we obtain information on local mixing under field conditions. Local dispersion is a decisive process that discriminates different flow regimes. The imaging device consists of a high-power xenon lamp and a sensitive charge coupled device (CCD) camera. The three fluorescent dyes Brilliant sulfaflavine (BF), Sulforhodamine B (SB), and Oxazine 170 (OX) were chosen as solute tracers for their spectroscopic properties and different sorption coefficients. We conducted a field experiment using these tracers and took images of their distribution in a vertical soil profile. The fluorescence images (1242 by 1152 pixels) were corrected for nonuniform lighting, changing surface roughness, and varying optical properties of the soil profile. The resulting two-dimensional relative concentration distributions were similar for BF and SB. The reason might be the fast transport regime, which prevents the establishment of sorption equilibria. According to its higher sorption coefficient, OX was more strongly retarded. In this paper, we show that the fluorescence imaging technique is a powerful tool for the in-situ investigation of transport processes of fluorescent solute tracers in soil profiles. Due to the high spatial resolution of the tracer concentration maps and the ability to detect the flow field characteristics of differently reactive tracers simultaneously under field conditions, this technique provides valuable experimental data for the test and development of theoretical models for heterogeneous solute transport in soils.

A two-stage procedure for bioequivalence studies.

A two-stage experimental procedure for bioequivalence studies is proposed. The procedure is based on the idea that information from a first-stage experiment can be used to form a predictive distribution for the outcome of a second-stage experiment, thus permitting an assessment of the probability of a successful overall outcome. A systematic numerical study of a variety of possible strategies results in the identification of procedures that lead to substantial increases in efficiency compared with single-stage studies.

Experiences in the application of NONMEM to pharmacokinetic data analysis.

Ethical issues arising from the use of patients in medical research have stimulated pharmacokinetic research in population kinetics, which requires only a few concentration samples of each individual. Using historical maprotiline data, the new approach of population kinetics was investigated and compared to individually estimated kinetics. Two different population kinetic methods were applied. The naive approach, a quick and dirty method, was compared to the nonlinear mixed-effects method, which was applied by the NONMEM package. Based on the results we obtained from actual maprotiline data as well as from simulated data, NONMEM is a reasonable tool for the estimation of population pharmacokinetic parameters. The main advantage of NONMEM over the naive approach lies in the possibility of obtaining standard deviations of random effects related to the variability between subjects.