Vol 50, No 13 (2016)

Macroevolutionary gains and losses in Bilateria are to a large extent controlled by the architecture of the gene regulatory network, including Hox- and other regulatory genes and also posttranscriptional regulation of microRNA. The concepts of evolutionary biology and reproduction strategy allow the recognition of different evolutionary strategy in Ecdysozoa and Deuterostomia. The emergence of numerous new populations of stem cells was a key evolutionary acquisition in Metazoa, especially in the evolutionary lineage of deuterostomes–chordates–vertebrates. The emergence of the neural plate interpreted as the fourth germ layer (neuroectoderm), with subsequent development of a hollow neural tube, was an aromorphic evolutionary innovation of vertebrates that provided the excess of neuroblasts and rapid evolution of the brain.

Referring the developmental canalization to stabilizing selection may be a bias that results from the ignorance of developmental mechanisms. Considering the morphological evolution of one-cell trichomes in Draba plants makes it clear that the transition from continuous variation in morphological traits to developmental creods occurs in the evolution of remote lineages of the genus irrespective of contribution to the net fitness. Morphological diversification of trichome branching is not under selection control, being a physical consequence of the trichome cell volume growth equilibrated by complication of the cell surface shape. At the start of evolution, the trichome development refers not to an individual trichome, but rather to repetitive trichome modules (branches), whose spatiotemporal order is arbitrary, except that some variants of branching depend on events that occur at earlier developmental stages more than others. Under selection fluctuating at random, or with no selection at all, fixing of these variants leads to the formation of trichome ontogeny, in which earlier developmental stages correspond to later stages of developmental evolution.

Pseudocyclic (P) integration was very important in the evolution of modular organisms. Its wide distribution was possible because of their morphogenesis, ontogeny, and systemic specifics. P-transformations are often related to changes around the boundaries of subsystems and structures, with a relatively low integrity of modular biosystems.

Deviations in the skeleton structure of radiolarians are extremely rare in the fossil record. They are known from the Devonian to Recent. This is a very ancient and periodically repeated phenomenon, which should be regarded as a regularity or “lost chance” rather than exotic or accident. Emergence of deviant “mutants” in radiolarians is probably connected with two main causes, i.e., disturbance during reproduction and mutations in particular modules. From the point of view of the morphogenesis of skeletal structures, deviancy facilitates the recognition of relatively “weak” modules–blocks in the general skeleton pattern, which are subject to structural changes. Nonheritable deviant variants have been revealed in skeletons of 61 radiolarian in all of three subphyla of the phylum Radiolaria: Polycystina, Phaeodaria, and Collodaria. Three deviant types are recognized: multiplicative, posterioric and supplemental.

A previously published sectional model of the system of tree branches (spruce) was expanded in the range (0,1) of the fractal model parameter μ, which links the value of green biomass of a “tree” to its size. The presence of branches in this range indicates the realization of green biomass in the form of photosynthe-sizing “points”, and is interpreted as endosymbiosis of cyanobacteria with protists. Using the method of box dimensionality, the parameter μ was estimated for the sets of points within an interval. The properties of the uniform and group distributions are shown to be different. For the group distribution, the trajectories of parameter μ are fundamentally different, depending on the method of point grouping, i.e., they decrease with an increase in the total number of points for a fixed number of points n_g in the groups and increase for a fixed number N_g groups. The initial endosymbiosis of cyanobacteria and “protists” is characterized by a lack of the necessary infrastructure in protists for feeding cyanobacteria and distributing their products and, thus, by a fixed number of “points” in the group. As the infrastructure of protists developed in the course of evolution, endosymbiosis tended to move towards an increased number of points in the group and, accordingly, increased μ. A special form of the dependence of parameter μ(N_g*n_g) provides the inherent nature of the initial growth deceleration and modularity of architecture, which are occasionally observed in extant plants.