Vol 50, No 14 (2016)

The turtle shell is characterized by a high degree of conservatism of the fundamental model and, at the same time, a high variability at the individual level. The components of the bony shell vary in origin. The costal and neural plates of the carapace are modified elements of the axial skeleton (ribs and neural arches) and the plastral plates are transformed dermal ossifications of the shoulder girdle and gastralia, peripheral, pygal, and suprapygal plates are similar to osteoderms of other reptiles. The variability of the structure of particular parts of the turtle shell is manifested differently. Most anomalies have been recorded in the caudal part of the carapace. The plastron is relatively stable in morphology. Variations in the bony shell structure are observed in (1) unusual shape and size of plates combined with normal number of plates, (2) presence of additional plates, and (3) absence of regular plates. Based on the morphogenetic characteris-tics, anomalies are subdivided into (1) variations caused by changes in the number of elements of the axial skeleton or their contacts with the dermis (neurals and costals); (2) variations due to changes in the number of horny scutes (peripherals); (3) variations connected with irregular osteogeny or disturbed growth of bones

Hair follicles (HF) are skin appendages that develop as a result of the epithelial-mesenchymal interactions. The HF mesenchymal component—dermal papilla (DP)—has an ability to induce HF growth after transplantation in afollicular epidermis; this ability is retained through several passages in culture. In the present study, early regeneration events of a human HF are designed in vitro, using DP cells and skin kerati-nocytes. An artificial hair germ model is developed to study the primary steps of the stem cell self-organiza-tion during HF regeneration.

The principal features of the morphogenesis in the individual and historical development of marine post-Paleozoic bryozoans of the order Tubuliporida (=Cyclostomata, part.) are discussed. Throughout their history (Ordovician–Recent), Tubuliporida retained the morphological type of the tubu-lar zooid with a terminal aperture. This may suggest similarities not only between the zooidal anatomy of fossil and living Tubuliporida but also between the ontogenetic processes in their ancestrulae and zooids and similarities in astogeny in general. After the two types of reproduction, sexual and vegetative, which lead to the formation of new colonies that could only grow by budding, had been developed, the develop-ment of different types of colonial organization was of special importance in the evolution of the post-Pale-ozoic Tubuliporida.

Convergence is observed in groups, which are phylogenetically remote. A flat test is typical for some representatives of the order Cassiduloida, such as Jurassic and Early Cretaceous species of the genera Pygurus and Clypeus, and also many Cenozoic «sand dollars,» i.e., echinoids of the order Clypeasteroida. Both usually inhabit coarse sandy grounds of shallow areas. The superorder Spatangacea includes the so-called Echinocorys life form, which is characterized by an oval test with superficial nonpetaloid or subpetaloid ambulacra, marginal or inframarginal periproct, and absence of fascioles. These are the following genera: Early Cretaceous Corthya (family Collyritidae), Late CretaceousLate Paleocene Echinocorys (family Holas-teridae), Paleocene Isaster, Recent Isopatagus (family Isasteridae), Recent Scrippsechinus (family Palaeotro-pidae), and Recent Urechinus (family Urechinidae). In contrast to the majority of spatangaceans with the burrowing mode of life, these genera dwell on the substrate surface. In the Cenozoic, the monobasal apical system appears in some genera of the order Spatangoida, most genera of the order Cassiduloida, all groups of the orders Clypeasteroida and Oligopygoida, and in the genus Echinoneus (order Holectypoida). The paral-lelism is revealed in groups connected by remote relationships. At the end of the Middle Jurassic (Callovian) and, especially, Late Jurassic, the so-called disasterid echinoids (superorder Spatangacea) show a distinct trend to the loss of contact between ocular plates I and V and apices of the posterior ambulacra with the periproct, which are shifted to the anterior part of the apical system (genera Collyrites, Collyropsis, Cyclolam-pas). At the same time, the peristome of some genera was displaced to the anterior margin of the test, which became bilaterally symmetrical in outline. However, in the Jurassic, all spatangaceans remained disasterid echinoids, i.e., had a disjunct apical system, which can be interpreted as a somewhat “abnormal” state. This trend disappeared only at the beginning of the Cretaceous, when “normal” forms with a joint apical system appeared, that is, the families Holasteridae (genera Eoholaster and Holaster, order Holasteroida) and Toxas-teridae (genus Toxaster, order Spatangoida). Interesting examples of synchronous parallelism are provided by the appearance of meridosternous (diasternal) plastron in two collyritid genera (Tetraromania and Corthya) in the Barremian, whereas in the holasterid genus Holaster, this type of plastron apparently appeared in the Valanginian (heterochronous parallelism). The ethmolitic type of the apical system appeared at the end of the Cretaceous and Paleocene at least in five families: Schizasteridae, Paleopneustidae, Brissidae, Spatangidae, and Loveniidae.

The importance of taking into account parallelisms in the evolution of morphological characters is analyzed for the taxonomy of the class Holothuroidea. The establishment of the order Dactylochirotida and classification of the order Elasipodida serve as examples to illustrate insufficient appreciation of parallelisms in Holothuroidea. The following characters, evolving independently in different groups of sea cucumbers, are considered: a stout skeleton, reduction of the calcareous ring and the body wall sclerites; similarity of body shape; similarity in the shape of tentacles; reduction in the number of tentacles from 12 to 10 in different fam-ilies and subfamilies of the order Synaptida. Based on the analysis of morphological and molecular data, the family Deimatidae is transferred from the order Elasipodida to the order Aspidochirotida. It is hypothesized that the concave cup-shaped sclerites with three to five rays occurring in the family Laetmogonidae (order Elasipodida) are of paedomorphic origin and correspond to the early growth stages of the laetmogonid wheels; the concave cross-shaped sclerites of the families Elpidiidae and Psychropotidae may have originated from laetmogonid concave cup-shaped sclerites. Emended diagnosis of the order Elasipodida is proposed. The family Vaneyellidae previously synonymized by the author with the family Cucumariidae is reestablished, and its emended diagnosis is also proposed.