Ammonium and nitrate uptake, nitrogen productivity and biomass allocation in interior spruce families with contrasting growth rates and mineral nutrient preconditioning.

Four full-sib families of interior spruce (Picea glauca (Moench) Voss) x Picea engelmanii Parry ex Engelm.) with contrasting growth rates (two fast-growing and two slow-growing families) were grown aeroponically with either a 2% relative nitrogen addition rate or free access to nitrogen. Fast-growing families showed greater plasticity in allocating biomass to shoots at high nitrogen supply and to roots at low nitrogen supply than slow-growing families. Compared with the slow-growing families, short-term net ammonium uptake rate measured with an ion selective electrode was significantly greater in fast-growing families at high ammonium supply, but not at low supply. Net nitrate uptake showed the same trend, but differences among families were not significant. Results indicate that differences in seedling growth rate are partly a result of physiological differences in net nitrogen uptake efficiency and nitrogen productivity.

Rapid quantitative pharmacodynamic imaging by a novel method: theory, simulation testing and proof of principle.

Pharmacological challenge imaging has mapped, but rarely quantified, the sensitivity of a biological system to a given drug. We describe a novel method called rapid quantitative pharmacodynamic imaging. This method combines pharmacokinetic-pharmacodynamic modeling, repeated small doses of a challenge drug over a short time scale, and functional imaging to rapidly provide quantitative estimates of drug sensitivity including EC 50 (the concentration of drug that produces half the maximum possible effect). We first test the method with simulated data, assuming a typical sigmoidal dose-response curve and assuming imperfect imaging that includes artifactual baseline signal drift and random error. With these few assumptions, rapid quantitative pharmacodynamic imaging reliably estimates EC 50 from the simulated data, except when noise overwhelms the drug effect or when the effect occurs only at high doses. In preliminary fMRI studies of primate brain using a dopamine agonist, the observed noise level is modest compared with observed drug effects, and a quantitative EC 50 can be obtained from some regional time-signal curves. Taken together, these results suggest that research and clinical applications for rapid quantitative pharmacodynamic imaging are realistic.