The method for determination of parameters of the phenomenological continual model of soil organic matter transformation

A possible method for experimental determination of parameters of the previously proposed continual mathematical model of soil organic matter transformation is theoretically considered in this paper. The previously proposed by the authors continual model of soil organic matter transformation, based on using the rate of matter transformation as a continual scale of its recalcitrance, describes the transformation process phenomenologically without going into detail of microbiological mechanisms of transformation. Thereby simplicity of the model is achieved. The model is represented in form of one differential equation in first­order partial derivatives, which has an analytical solution in elementary functions. The model equation contains a small number of empirical parameters which generally characterize environmental conditions where the matter transformation process occurs and initial properties of the plant litter. Given the values of these parameters, it is possible to calculate dynamics of soil organic matter stocks and its distribution over transformation rate. In the present study, possible approaches for determination of the model parameters are considered and a simple method of their experimental measurement is proposed. An experiment of an incubation of chemically homogeneous samples in soil and multiple sequential measurement of the sample mass loss with time is proposed. An equation of time dynamics of mass loss of incubated homogeneous sample is derived from the basic assumption of the presented soil organic matter transformation model. Thus, fitting by the least squares method the parameters of sample mass loss curve calculated according the proposed mass loss dynamics equation allows to determine the parameters of the general equation of soil organic transformation model

Unanimous Model for Describing the Fast Bioluminescence Kinetics of Ca²⁺-regulated Photoproteins of Different Organisms

Upon binding their metal ion cofactors, Ca2+-regulated photoproteins display a rapid increase of light signal, which reaches its peak within milliseconds. In the present study, we investigate bioluminescence kinetics of the entire photoprotein family. All five recombinant hydromedusan Ca2+-regulated photoproteins-aequorin from Aequorea victoria, clytin from Clytia gregaria, mitrocomin from Mitrocoma cellularia and obelins from Obelia longissima and Obelia geniculata-demonstrate the same bioluminescent kinetics pattern. Based on these findings, for the first time we propose a unanimous kinetic model describing the bioluminescence mechanism of Ca2+-regulated photoproteins