Animal testing and its alternatives - the most important omics is economics.

For a long time, the discussion about animal testing vs its alternatives centered on animal welfare. This was a static warfare, or at least a gridlock, where life scientists had to take a position and make their value choices and hardly anyone changed sides. Technical advances have changed the frontline somewhat, with in vitro and in silico methods gaining more ground. Only more recently has the economic view begun to have an impact: Many animal tests are simply too costly, take too long, and give misleading results. As an extension and update to previous articles in this series written a decade ago, we reanalyze the economic landscape of especially regulatory use of animal testing and this time also consider respective alternative tests. Despite some ambiguity and data gaps, which we have filled with crude estimates, a picture emerges of globally regulated industries that are subject to stark geographic and sectorial differences in regulation, which determine their corresponding animal use. Both animal testing and its alternatives are industries in their own right, offering remarkable business opportunities for biotech and IT companies as well as contract research organizations. In light of recent revelations as to the reproducibility and relevance issues of many animal tests, the economic consequences of incorrect results and the reasons for still maintaining often outdated animal test approaches are discussed.

Experimental visualization of solute transport and mass transfer processes in two-dimensional conductivity fields with connected regions of high conductivity.

Solute transport displaying mass transfer behavior (i.e., tailing) occurs in many aquifers and soils. Spatial patterns of hydraulic conductivity may play a role because of both advection and diffusion through isolated low conductivity areas. We demonstrated such processes in laboratory experiments designed to visualize solute transport through a thin chamber (40 cm x 20 cm x 0.64 cm thick) packed with glass beads and containing circular emplacements of smaller glass beads with lower conductivity. The experiments used three different contrasts of conductivity between the large-bead matrix and the emplacements, targeting three different regimes of solute transport: low contrast, targeting macrodispersion; intermediate contrast, targeting advection-dominated mass transfer between the high-conductivity regions and the emplacements; and high contrast, targeting diffusion-dominated mass transfer. Use of a strong light source, a high-resolution CCD camera, and a colorimetric dye produced images with a spatial resolution of about 400 microm and a concentration range of approximately 2 orders of magnitude. These images confirm the existence of the three different regimes, and we observed tailing driven by both advection and diffusion. Outflow concentration measured by spectrophotometer achieved 3 orders of magnitude in concentration range and showed good agreement with known models in the case of dispersion and diffusive mass transfer, with estimated parameters close to a priori predictions. Existing models for diffusive mass transfer did notfitthe breakthrough curves from the intermediate-contrast chamber, but a model of slow advection through cylinders did. Thus, both breakthrough curves and chamber images confirm that different contrasts in small-scale K lead to different regimes of solute transport and thus require different models of upscaled solute transport.

Reactive transport in porous media: a comparison of model prediction with laboratory visualization.

Groundwater transport models that accurately describe spreading of nonreactive solutes in an aquifer can poorly predict concentrations of reactive solutes. The dispersive term in the advection-dispersion equation can overpredict pore-scale mixing, and thereby overpredict homogeneous chemical reaction. We quantified this experimentally by imaging instantaneous colorimetric reactions between solutions of aqueous CuSO4 and EDTA4- within a 30-cm long translucent chamber packed with cryolite sand that closely matched the optical index of refraction of water. A charge-coupled device camera was used to quantify concentrations of blue CuEDTA2- within the chamber as it was produced by mixing of the two reactants at different flow rates. We compared these experimental results with a new analytic solution for instantaneous bimolecular reaction coupled with advection and dispersion of the product and reactants. For all flow rates, the concentrations of CuEDTA2- recorded in the experiments were about 20% less than predicted by the analytic solution, thereby demonstrating that models assuming complete mixing at the pore scale can overpredict reaction during transport.