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M J Whelan

Publications and source records attributed to M J Whelan.

3 recordsLinked to original sources

Stochastic modelling of phosphorus transfers from agricultural land to aquatic ecosystems.

This paper describes a simple model of phosphorus (P) transfer from agricultural land to surface waters which incorporates the effects of spatial variability in catchment properties and uncertainty in model parameter values. TOPMODEL concepts are used to estimate water, solute and sediment fluxes to water bodies. The model predicts the spatial distribution of water table depth and saturation-excess overland flow based on topography. Dissolved P (DP) transfer is assumed to occur vertically in the unsaturated zone and laterally in the saturated zone. Readily soluble P is assumed to decrease exponentially with soil depth. Particulate P (PP) transfers are modelled by estimating overland flow discharge and associated sediment transport capacity. Uncertainty in the distribution of soil surface P concentrations and model parameters controlling the mobility of soil P are incorporated using Monte Carlo simulation. Predicted losses of DP are well correlated with discharge and those of PP are episodic. Highest losses of P tended to be predicted near to the stream where the water table is close to the surface. The combination of a deterministic model core with a stochastic generation of model parameters or state variables provides an attractive way of embracing variability and uncertainty in models of this kind.

Agriculture↗

The influence of polyvinylpyrrolidone on the solution and bioavailability of hydrochlorothiazide.

The dissolution properties of hydrochlorothiazide-PVP 10 000 mechanical mix and coprecipitate systems were qualitatively similar to those previously reported using hydroflumethiazide. Quantitative differences were dependent on the proportion of PVP present, its molecular weight and method of incorporation. Cumulative urinary excretion data from test capsule preparations showed that bioavailability was enhanced by the presence of PVP. However, the degree of enhancement was less than that expected from constant surface area disc rate studies. Dissolution tests on the capsule formulations, using the U.S.P. basket stirrer assembly, did not correlate with in vivo results. Using the Levy beaker method and a stirring speed of 40 rev min-1, good correlation between amount dissolved in 30 min and amount excreted in urine after 24 h was obtained. The dissolution tests revealed that PVP retards the initial dissolution from capsule dosage forms, probably by retarding deaggregation and dispersion of drug particles.

Adult↗