Katarzyna Janiszewska

A unique skeletal microstructure of the deep‐sea micrabaciid scleractinian corals

Micrabaciids are solitary, exclusively azooxanthellate deep‐sea corals belonging to one of the deepest‐living (up to 5,000 m) scleractinian representatives. All modern micrabaciid taxa (genera: Letepsammia, Rhombopsammia, Stephanophyllia, Leptopenus) have a porous and often very fragile skeleton consisting of two main microstructural components known also from other scleractinians: rapid accretion deposits and thickening deposits. However, at the microstructural level, the skeletal organization of the micrabaciids is distinctly different from that of other scleractinians. Rapid accretion deposits consist of alternations of superimposed “microcrystalline” (micrometer‐sized aggregates of nodular nanodomains) and fibrous zones. In contrast to all shallow‐water and sympatric deep‐water corals so far described, the thickening deposits of micrabaciids are composed of irregular meshwork of short (1–2 μm) and extremely thin (ca. 100–300 nm) fibers organized into small, chip‐like bundles (ca. 1–2 μm thick). Longer axes of fiber bundles are usually subparallel to the skeletal surfaces and oriented variably in this plane. The unique microstructural organization of the micrabaciid skeleton is consistent with their monophyletic status based on macromorphological and molecular data, and points to a diversity of organic matrix‐mediated biomineralization strategies in Scleractinia. J. Morphol.,2011.

Upper Permian Vertebrate Coprolites from Vyazniki and Gorokhovets, Vyatkian Regional Stage, Russian Platform

Abstract Numerous coprolites have been found in the Vyazniki and Gorokhovets localities of European Russia. Five identified coprolite-bearing horizons occur in the upper Permian deposits of the Vyatkian Regional Stage. Coprolites were collected from mudstone with a coprolite breccia-like layer and also from intraformational conglomerates that were deposited in a floodplain and overbank environment. Two coprolite morphotypes (A and B) are recognized from size and shape analysis of 32 specimens. Morphotype A has long, nonsegmented feces. Smaller, cylindrical or tubular-shaped coprolites of morphotype B are commonly segmented. SEM images of the coprolite matrix show spheres and thin-walled vesicles with diameters 0.5–4 µm. Electron Micro Probe (EMP) analyses of polished thin sections show microcrystalline carbonate-fluoride-bearing calcium phosphate with small amounts of calcium replaced in the crystal lattice. Optical microscopy and EMP investigations show that iron and manganese oxides are responsible for elevated iron and manganese concentrations in the bulk mass of coprolites. Other metals (V, Ni) can be associated with oxides forming spheroids with diameters 3–10 µm. REEs (rare earth elements, U, and other trace element concentrations suggest significant eolian sediment input to the burial environment of the coprolites. The scats contain fish scales and bones of tetrapods (amphibians or reptiles). In one large-sized coprolite, a small fragment of therapsid bone was also found. Both morphotypes are matched to carnivorous taxa within the Archosaurus rossicus zone of the Eastern Europe. The size and shape of the best-preserved specimens suggest that they were possibly produced by a large therapsid, anthracosaur, or early archosauromorph predator.

Simultaneous extension of both basic microstructural components in scleractinian coral skeleton during night and daytime, visualized by in situ 86Sr pulse labeling.

Using in situ (12h) pulse-labeling of scleractinian coral aragonitic skeleton with stable 86Sr isotope, the diel pattern of skeletal extension was investigated in the massive Porites lobata species, grown at 5 meters depth in the Gulf of Eilat. Several microstructural aspects of coral biomineralization were elucidated, among which the most significant is simultaneous extension of the two basic microstructural components Rapid Accretion Deposits (RAD; also called Centers of Calcification) and Thickening Deposits (TD; also called fibers), both at night and during daytime. Increased thickness of the 86Sr-labeled growth-front in the RADs compared to the adjacent TDs revealed that in this species RADs extend on average twice as fast as TDs. At the level of the individual corallite, skeletal extension is spatially highly heterogeneous, with sporadic slowing or cessation depending on growth directions and skeletal structure morphology. Daytime photosynthesis by symbiotic dinoflagellates is widely acknowledged to substantially increase calcification rates at the colony and the corallite level in reef-building corals. However, in our study, the average night-time extension rate (visualized in three successive 12h pulses) was similar to the average daytime extension (visualized in the initial 12h pulse), in all growth directions and skeletal structures. This research provides a platform for further investigations into the temporal calibration of coral skeletal extension via cyclic growth increment deposition, which is a hallmark of coral biomineralization.

Aragonitic scleractinian corals in the Cretaceous calcitic sea

Changes in seawater chemistry have affected the evolution of calcifying marine organisms, including their skeletal polymorph (calcite versus aragonite), which is believed to have been strongly influenced by the Mg/Ca ratio at the time these animals first emerged. However, we show that micrabaciids, a scleractinian coral clade that first appeared in the fossil record of the Cretaceous, when the ocean Mg/Ca ratio was near the lowest in the Phanerozoic (thus a priori favoring calcitic mineralogy), formed skeletons composed exclusively of aragonite. Exceptionally preserved aragonitic coralla of Micrabacia from the Late Cretaceous Ripley Formation (southeastern USA) have skeletal microstructures identical to their modern representatives. In addition, skeletons of Micrabacia from Cretaceous chalk deposits of eastern Poland are clearly diagenetically altered in a manner consistent with originally aragonitic mineralogy. These deposits have also preserved fossils of the scleractinian Coelosmilia, the skeleton of which is interpreted as originally calcitic. These findings show that if changes in seawater Mg/Ca ratio influenced the mineralogy of scleractinian corals, the outcome was taxon specific. The aragonitic mineralogy, unique skeletal microstructures and ultrastructures, and low Mg/Ca ratios in both fossil and living micrabaciids indicate that their biomineralization process is strongly controlled and has withstood major fluctuations in seawater chemistry during the past 70 m.y.

Skeletal Ontogeny in Basal Scleractinian Micrabaciid Corals

The skeletal ontogeny of the Micrabaciidae, one of two modern basal scleractinian lineages, is herein reconstructed based on serial micro‐computed tomography sections and scanning electron micrographs. Similar to other scleractinians, skeletal growth of micrabaciids starts from the simultaneous formation of six primary septa. New septa of consecutive cycles arise between septa of the preceding cycles from unique wedge‐shaped invaginations of the wall. The invagination of wall and formation of septa are accompanied by development of costae alternating in position with septa. During corallite growth, deepening invagination of the wall results in elevation of septa above the level of a horizontal base. The corallite wall is regularly perforated thus invaginated regions consist of pillars inclined downwardly and outwardly from the lower septal margins. Shortly after formation of septa (S2 and higher cycles) their upper margins bend and fuse with the neighboring members of a previous cycle, resulting in a unique septal pattern, formerly misinterpreted as “septal bifurcation.” Septa as in other Scleractinia are hexamerally arranged in cycles. However, starting from the quaternaries, septa within single cycles do not appear simultaneously but are inserted in pairs and successively flank the members of a preceding cycle, invariably starting from those in the outermost parts of the septal system. In each pair, the septum adjacent to older septa arises first (e.g., the quinaries between S2 and S4 before quinaries between S3 and S4). Unique features of micrabaciid skeletal ontogeny are congruent with their basal position in scleractinian phylogeny, which was previously supported by microstructural and molecular data. J. Morphol., 2013.

Two types of bone necrosis in the Middle Triassic Pistosaurus longaevus bones: the results of integrated studies

Avascular necrosis, diagnosed on the basis of either a specific pathological modification of the articular surfaces of bone or its radiologic appearance in vertebral centra, has been recognized in many Mesozoic marine reptiles as well as in present-day marine mammals. Its presence in the zoological and paleontologic record is usually associated with decompression syndrome, a disease that affects secondarily aquatic vertebrates that could dive. Bone necrosis can also be caused by infectious processes, but it differs in appearance from decompression syndrome-associated aseptic necrosis. Herein, we report evidence of septic necrosis in the proximal articular surface of the femur of a marine reptile, Pistosaurus longaevus, from the Middle Triassic of Poland and Germany. This is the oldest recognition of septic necrosis associated with septic arthritis in the fossil record so far, and the mineralogical composition of pathologically altered bone is described herein in detail. The occurrence of septic necrosis is contrasted with decompression syndrome-associated avascular necrosis, also described in Pistosaurus longaevus bone from Middle Triassic of Germany.

Tuberculosis-like respiratory infection in 245-million-year-old marine reptile suggested by bone pathologies

An absence of ancient archaeological and palaeontological evidence of pneumonia contrasts with its recognition in the more recent archaeological record. We document an apparent infection-mediated periosteal reaction affecting the dorsal ribs in a Middle Triassic eosauropterygian historically referred to as ‘Proneusticosaurus’ silesiacus. High-resolution X-ray microtomography and histological studies of the pathologically altered ribs revealed the presence of a continuous solid periosteal reaction with multiple superficial blebs (protrusions) on the visceral surfaces of several ribs. Increased vascularization and uneven lines of arrested growth document that the pathology was the result of a multi-seasonal disease. While visceral surface localization of this periosteal reaction represents the earliest identified evidence for pneumonia, the blebs may have an additional implication: they have only been previously recognized in humans with tuberculosis (TB). Along with this diagnosis is the presence of focal vertebral erosions, parsimoniously compared to vertebral manifestation of TB in humans.