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The forecasts at that time of a population explosion had an adverse impact on the programme.
To determine the mean generation time of a population, the age of the individuals (x) is multiplied by the proportion of females surviving to that age (lx) and the average number of offspring left by females at that age (mx).
In S. cerevisiae two different paradigms are used to measure longevity: the replicative life span, which is defined as the total number of daughter cells generated by a mother cell; and the chronological life span which is measured by monitoring the mean/maximum survival time of a population of non-dividing yeast.
The fall germination time of a population cohort can also affect flowering time under basic greenhouse conditions with only minimal temperature augmentation (Botto and Coluccio 2007).
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Demographers or sociologists of population study the size, composition and change over time of a given population.
For the analysis of temporal changes in allele frequencies for Ne estimation, the program NeESTIMATOR requires the user to define a reference time point of a population (generation 0) and at least one subsequent generation (in our case generation 1).
We then developed models to predict the developmental time of a cell population given its transcriptional profile.
The mean of the ten vials was taken as an estimate of the developmental time of a given population at a given temperature.
Chronological life span (CLS) is a measure of the length of time a population of yeast cells can remain in stationary phase before they lose the ability to restart growth following re-inoculation into fresh media.
Our main interest is in describing the large-time behavior of a population provided that we know its initial distribution and transient vital rates.
Decreasing the population size allows the simulation of a greater number of generations in a reasonable amount of time: a population size of 10 000 takes ∼3 s/100 generations (without selection, with a slight increase with selection).
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