m.r.Life ι**=7/3ψ

Protozoa - the interacting self-replicating cell

Interacting self-replicating cells with advanced metabolic pathways (like protozoa) can be naturally selected by an incomplete population dynamic feed-back selection

Metabolism, net energy, interference and mass: The minimum self-replicator can evolve into larger self-replicating cells with more complete metabolic pathways by the gradual unfolding of an interactive competition that bias the resource access in favour of the individuals with a larger than average mass (Witting, 2017b).

With selection for interactive behaviour, the cost gradient (ψ) of interactive competition is increasing. This is generating a bias in the distribution of net energy [ ε (wi/w)ψι with ψι > 0 ] that reflects that the larger (wi) than average (w) individuals monopolise (ψ) the resource to some degree. This emergence of a resource bias selects for larger self-replicating cells with higher rates of mass specific metabolism; as defined by the β-dependent minimum mass that is required to sustain a pre-mass mass specific metabolism that increases sub-linearly with mass [ ββ = 1 - ψι* ]. This selection can continue with a maximal resource bias exponent that increases towards unity [ ψι* → 1 ], causing the evolution of a self-replicating cell with fully developed metabolic pathways and a ββ exponent of zero.

This partial unfolding of population dynamic feed-back selection is illustrated in Fig. 1, right. With a maximal resource bias exponent below unity, the interactive competition is not yet so strong that it can select mass independently of the dependence of mass specific metabolism on mass. The result is a mass that is still being selected as a β-dependent minimum. This implies maximal interference and an incomplete unidirectional feed-back; where interference is influencing the selection of mass, but where the level of interference is unaffected by the selection of mass.

Fig. 1 Left: Body mass (w) allometry for mass specific metabolism (β) in 52 species of protozoa. A least squares fitted third order polynomial estimates a b exponent that declines from 0.61 over zero to -0.20 with an increasing mass. From Witting (2017a), data from DeLong et al. (2010); 4 outliers removed. Right: An illustration of the partial feed-back selection that predicts a 3D b exponent that declines from 0.83 over zero to -0.17 for an asexual self-replicating cell. The selected β-dependent minimum mass (wβ), generates maximal population growth (r), and a density regulated (γ) abundance (n*) with a maximal resource bias below unity (0 < ψι** < 1). This maximum bias assists in the selection of mass, but it is too weak to generate a complete feed-back, where it is the interactive selection of mass that is determining the level of interference in the population.

Allometries: Having a pre-mass exponent (ββ) for mass specific metabolism that evolves from unity to zero, the predicted allometric exponent for mass specific metabolism b = ββ + βw is declining from 5/6 (≈0.83) over zero to -1/6 (≈-0.17), because βw=-1/6 for three dimensional interactions (Witting, 1995, 2017a). This coincides with an empirically estimated exponent that declines from 0.61 over zero to -0.20 across protozoa with an increasing mass (Fig. 1, left).

Life history: With a β-dependent minimum mass, these interacting protozoa-like self-replicators are selected to have a single cell only. And with a maximal resource bias below unity, they are, as prokaryotes, selected to have asexual reproduction (Witting, 1997, 2002). A difference is the more fully developed metabolic pathways in protozoa, and the evolution of a more active interactive behaviour, as well as a more active handling of their resources (Witting, 2017b).

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Ecology and Evolution 7:9098-9118 (2017)Download

The natural selection of metabolism and mass selects lifeforms from viruses to multicellular animals


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