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Retained colour pattern on the shells of Plectodonta sp. from the earliest Devonian of Podolia (Ukraine) is the first finding for strophomenide brachiopods and the oldest among articulate brachiopods. The colour pattern in Plectodonta sp. is composed of small, round, brownish spots scattered rather irregularly on the ventral valve only. This may suggest that the described pattern probably performed a protective function through disruptive camouflage against visual systems of potential predators. The occurrence of the colour pattern in Plectodonta sp. exclusively on the ventral valve strongly suggests that these brachiopods lived with the patterned (and convex) ventral valve upwards and the patternless concave dorsal valve facing to the underlying substrate. It thus contradicts a general assumption that concavo−convex brachiopods lived with their convex valves resting on the sediment.
In the Podolian Dniester Basin (southwestern Ukraine) the Lower Devonian marine deposits are represented by about 530 m thick continuous sequence of interlaminated carbonate and schale outcrops at several localities. Conodonts occur in most of the carbonate layers of the whole Lochkovian but are not abundant and their ramiform elements are mostly broken or lacking. Therefore, only the pectiniform, Pa elements of twenty five stratigraphically important conodont species occurring in the region are discussed and two new species, Caudicriodus schoenlaubi and Pandorinellina? parva are proposed. The hypothetical phyletic relationships within the main representatives of the icriodontid and spathognathodontid genera, Caudicriodus, Zieglerodina, and Pandorinellina? are traced. Comparison of the previously published and newly obtained data revealed discrepancies in the hitherto used interpretation of some of the conodont taxa and their stratigraphic ranges. Contrary to the earlier reports, Caudicriodus postwoschmidti does not occur in the lower Lochkovian but only in the middle part of the Chortkiv Formation, high above the Monograptus uniformis Zone. Based on new material and verification of the previous determinations, a modified scheme of the Lochkovian conodont zonation in Podolia is proposed. Conodont zones: Caudicriodus hesperius, C. transiens, C. postwoschmidti, C. serus, and ?Caudicriodus steinachensis are distinguished. The zones are correlated with conodont zonations in other regions—Barrandian, Cantabrian Mountains, Pyrenees, and Nevada. Biostratigraphy of the Siluro−Devonian transition and Lochkovian is integrated with the carbon isotope stratigraphy.
Ischnacanthiform acanthodian dentigerous jaw bones from the Lower Devonian (Late Lochkovian) of Podolia are described for the first time. One new genus and one new species are established. Podoliacanthus gen. nov. is diagnosed as having small−sized jaw bones, the presence of specific accessory cusps/denticles on the medial side of teeth of the lateral tooth row, and groups of denticles forming the lingual tooth row. Podoliacanthus zychisp. nov. is distinguished in having elongated slender jaw bones and lateral teeth with one medial side denticle. Besides, three species are described in open nomenclature: Podoliacanthus sp. 1, while similar to Podoliacanthus zychi sp. nov., differs in having stronger posterior inclination of the teeth tips and presence of well developed flanges of the teeth, P. sp. 2 has quite robust jaw bones and teeth with two medial side denticles, and Podoliacanthus sp. 3 has small narrow jaw bones and teeth with three medial side denticles. Morphology of the lingual tooth row is considered to be a diagnostic feature of generic and higher taxonomic levels, while accessory medial cusps/denticles of the teeth are regarded as diagnostic features at species level. The new genus also occurs in Upper Silurian or Lower Devonian deposits of North Greenland. Preservation of the jaw bones possibly depends on their secondary mineralization.
Investigation of mixed carbonate−siliciclastic Lower Devonian deposits have been carried out in the Ivanye Zolote and Ustechko sections in Podolia, Ukraine. Based on palynomorph evidence, the age of the samples studied is late Lochkovian, not older than the NM Oppel Miospore Zone, specifically the Si Lineage Zone. The presence of acritarchs and chitinozoans points to dominantly marine depositional conditions. However, a regressive environmental change toward more brackish conditions is indicated by a decrease in the taxonomic diversity of acritarchs in the topmost samples, the simultaneous disappearance of chitinozoans, and an increase in leiosphaerid frequency. Furthermore, evolution of limestone microfacies demonstrates a progressive transition from a shrinking marine basin toward a brackish, storm−affected muddy lagoon, manifested by recurrent profusion of impoverished, mostly opportunistic and euryhaline shelly benthos (nuculanid bivalves, leperditicopids and other ostracods, terebratulid brachiopods), chaetetid demosponges and diverse ichthyofauna. The association of plant (mainly nematophytes and some tracheids) and animal (eurypterid, ?scorpion, and possibly other arthropod) remains points to the presence of nearby Early Devonian wetland vegetation, providing food and shelter for various semi−aquatic and other terrestrial arthropods.
In the classic section across the Silurian–Devonian boundary at Dnistrove (Podolia, Ukraine) the brachiopod fauna has never been studied in detail. This paper presents results of research on brachiopods from this important locality and time interval. Bed−by−bed collecting has enabled the detailed distribution of brachiopod taxa through the boundary beds to be revealed. Generally, the reference section at Dnistrove yields rather scarce but often well preserved brachiopods. Dayia bohemica and Dnestrina gutta can be regarded as characteristic species for the uppermost Silurian. A relatively high−diversity but low−abundance brachiopod fauna occurs in the lowest 1.8 m of the earliest Devonian. Only three forms have been found to cross the Silurian–Devonian boundary: the strophomenide Plectodonta (Plectodonta) mariae pantherae subsp. nov., the atrypide Gracianella (Sublepida) paulula sp. nov., and the spiriferide Howellella (Howellella) latisinuata. A relatively narrow brachiopod−rich interval at 5.5 m above the Silurian–Devonian boundary yields 16 brachiopod species which probably indicate a setting near the lower limit of the photic zone equivalent to the Benthic Assemblage 3–4 boundary. Two new species and one new subspecies are described: Skenidioides tatyanae, Plectodonta (Plectodonta) mariae pantherae, and Gracianella (Sublepida) paulula.
Colonies of boring ctenostome bryozoans and microborings of “fungi” that occur in the Early Devonian (Lochkovian, ~416 Ma) of Podolia, western Ukraine, have soft−tissue preserved by phosphatization. These comprise exceptional three−dimensional body walls of feeding zooids with probable parietal muscles inserted on the cystid wall, and setigerous collars twisted within the vestibulum. The presence of collars in this Early Devonian ctenostomes proves the existence of this feature for more than 416 Ma of ctenostome evolution. Phosphatized remains of the zooid walls are interpreted as relicts of the originally chitinous cystid walls. This is the first record of soft−tissue fossilization in a boring bryozoan. The presence of cavities (specialized heterozooids), empty or filled with laminated calcium phosphate, is also documented in bryozoans for the first time. These cavities are interpreted as “store−rooms” in which the bryozoans accumulated nutrients. The new taxon, Podoliapora doroshevi gen. et sp. nov. is described. In additional, phosphatised fungi−like endoliths co−occur with bryozoans.
Two global isotopic events, the early Sheinwoodian (early Wenlock) and that at the Silurian–Devonian transition, have been comprehensively studied in representative carbonate successions at Kytayhorod and Dnistrove, respectively, in Podolia, Ukraine, to compare geochemistry and biotic changes related correspondingly to the Ireviken and Klonk events. These two large−scale isotope excursions reveal different regional ecosystem tendencies. The well−defined increasing trend across the Llandovery–Wenlock boundary in siliciclastic input, redox states and, supposedly, bioproductivity, was without strict correlative relations to the major ¹³C enrichment event. The environmental and biotic evolution was forced by eustatic sea−level fluctuations and two−step climate change toward a glaciation episode, but strongly modified by regional epeirogeny movements due to location near the mobile Teisseyre−Törnquist Fault Zone. Thus, the global early Sheinwoodian biogeochemical perturbation was of minor depositional significance in this epeiric sea, as in many other Laurussian domains. Conversely, the Podolian sedimentary record of the Klonk Event exhibits temporal links to the abrupt δ¹³C anomaly, overprinted by a tectonically driven deepening pulse in the crucial S–D boundary interval. This carbon cycling turnover was reflected in the regional carbonate crisis and cooling episodes, paired with a tendency towards eutrophication and recurrent oxygen deficiency, but also with major storms and possible upwelling. Faunal responses in both Podolian sections follow some characters of the Silurian pattern worldwide, as manifested by conodont changeover prior to the major early Sheinwoodian isotopic/climatic anomaly. This contrasts with the relative brachiopod and chitinozoan resistances in the course of the Ireviken Event. Also, during the Klonk Event, a moderate faunal turnover, both in benthic and pelagic groups, occurred only near the very beginning of the prolonged ¹³C−enriched timespan across the system boundary, possibly due to progressive dysoxia and temperature drop. The characters point to a peculiarity of the Klonk Event by comparison with the Silurian global events, and some similarity already to the succeeding Devonian transgressive/anoxic episodes.
New osteostracans (Agnatha, Osteostraci) Zenaspis dzieduszyckii sp. nov. and Wladysagitta janvieri gen. et sp. nov., as well as new form of Diademaspis are described from the Lower Devonian of Podolia (Ukraine). Among them Zenaspis dzieduszyckiisp. nov. differs from all other representatives of the genus by its smaller overall size and relatively larger orbits. Wladysagitta janvieri is remarkable by having a rostral process. This new species together with “Cephalaspis” acutirostris Stensiö, 1932 from Old Red deposits of Shropshire (Great Britain) are proposed to be united under common generic name Wladysagitta. Since Diademaspis sp. is completely unknown in outline of its shield, it could not be named as new species, although it should be a really new form. New diagnostic features, such as relative width of the orbits, relative width of the dorsal field, and the position of the posterior end of the lateral fields relatively to the margins of the headshield, are proposed to differentiate genera within the Zenaspididae. Probably, the rostral process of osteostracans should be considered as a multifunctional device having at least a sensory function for food−search, possibly hydrodynamic functions, or may play a role in scaring predators.
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