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Trace fossils Lockeia siliquaria James, Ophiomorpha nodosa Lundgren, Para- taenidium seymourensis isp. n., Protovirgularia rugosa (Miller and Dyer) and Rhizo- corallium jenense Zenker have been described for the first time from the Eocene La Meseta Formation of Seymour (Marambio) Island, Antarctic Peninsula. Determinations of some trace fossils formerly described from this formation have been revised. The whole trace fossils association from the La Meseta Formation points to foreshore-offshore environment as indicated by presence of the Skolithos and Cruziana ichnofacies, and to at least temporal normal salinity.
Y−shaped trace fossil (U−shaped upper part with a basal shaft), Parmaichnus stironensis igen. nov. et isp. nov. penetrates from a discontinuity surface cut in Early Quaternary mudstones in the Stirone Valley, Northern Italy. It is attributed to upogebiid decapod crustaceans. Parmaichnus differs from Psilonichnus by the presence of turning chambers in the upper part of the burrow. The turning chambers are considered to be an important taxonomic feature of upogebiid burrows. P. stironensis occurs together with Thalassinoides cf. paradoxicus (produced probably by callianassid crustaceans) and wide U−shaped pyritised cylinders (supposedly produced by balanoglossid hemichordates).
We describe and interpret Undichna septemsulcata isp. nov., from the fluvial Old Red Sandstone deposits of the Early Devonian Wood Bay Formation, of Northern Spitsbergen (Svalbard). Its delicate scratch pattern, comprising one unpaired median groove and three pairs of lateral grooves, all with a regular in−phase sinusoidal wave pattern of equal wavelength, allow the reconstruction of the number, position and relative spacing of the fins. The comparatively high−amplitude median groove is attributed to the main propelling action of the tail or caudal fin, the inner pair of the lateral grooves to the action of the pelvic fins, and the low−amplitude outer set of duplicate grooves to bifurcated pectoral fins, respectively. The in−phase geometric pattern is explained by a distance between the unpaired fin (caudal or anal fin) to the pectoral fins corresponding to one wavelength and a position of the pelvic fins half way in between. The direction of movement and the mode of locomotion of the trace maker (a carangiform to ostraciiform type) are deduced. This analysis is leading to an acanthodian (possibly Diplacanthus) as the most probable trace maker. By being Pragian or early Emsian (Early Devonian) in age, according to vertebrate and palynomorph biostratigraphy, these specimens are among the world’s oldest trace fossils made by a vertebrate.
Several specimens of trace fossil Bichordites monastiriensis were discovered in two shallow water Oligocene sandstone beds from Valsugana (Trentino, NE Italy) representing the oldest documented occurrence for this ichnospecies. They are grazing−crawling (pascichnion−repichnion) structures and are occasionally associated with enlarged structures that can be interpreted as resting traces (cubichnia) and assigned to the ichnogenus Cardioichnus. The resulting Bichordites–Cardioichnus compound trace fossil is here described for the first time. In the basal part of some specimens, skeletal remains of Eupatagus ornatus were found in life position. This founding enables to widen the spectrum of known Bichordites tracemakers. Exceptional conditions of preservation of one specimen extending in two beds recording different environmental conditions gave an opportunity to document the effects of various taphonomical histories on the preservation of this traces.
From the Early Maastrichtian white chalk of Rügen Island (N Germany), a specimen of the echinoid Echinocorys ovata featuring 27 boring traces of the ichnogenus Caulostrepsis is described. Individual traces are shallow to moderately deep U−shaped depressions and show distinct regeneration textures evidencing a syn−vivo infestation. All traces are located on the plastron between the peristome and periproct of the host echinoid, indicating an adaptation of the trace maker by choosing the most advantageous position of the specific host. The traces are attributed to the work of boring spionid polychaetes (Polydora complex), grounded on the close morphological resemblance with initial borings of Recent polydorids. This is the first evidence for a possible association of a boring polychaete not only with an echinoid but with an echinoderm in general. The symbiotic relationship was commensalistic in nature with the spionid probably taking advantage of organic matter resuspended by the echinoids locomotion and feeding activity and benefiting from effective shelter. For the host echinoid, the association was moderately harmful. The soft bottom environment of the chalk sea provided very limited hard substrate ecospace for settlers and bioeroders, available only in form of biogenic structures. Echinocorys was a dominant component of this benthic community and can be considered as a suitable host for symbiotic interactions because of its size and assumed longevity.
The radial trace fossil Dactyloidites peniculus occurs in a deep tier in totally bioturbated shoreface sediments of Pliocene age in the Stirone Valley, N Italy, together with Thalassinoides isp. and Ophiomorpha nodosa. Long, narrow shafts running from centre of the radiating structure and abundant faecal pellets in the radial structure were discovered. The trace maker of D. peniculus, probably a polychaete, deposited the pellets deeply in the sediment, probably for reinforcement of the tubes and a gardening of microbes for feeding. This trace fossil exclusively occurs within a narrow horizon at the top of a shallowing−up section interpreted as a high−stand system tract, below a discontinuity surface capped by finer sediments. D. peniculus was formed in soft sandy sediments under stable conditions related to the latest phases of the highstand system tract. Therefore, it is a candidate for indication of similar environmental situations having a soft sandy, but stable sea floor.
The marine Pliocene at the locality of Nefiach (Roussillon Basin, SE France) includes several shell beds constituted by oysters and scallops that bear a diverse and abundant bioerosion trace fossil assemblage. The most abundant trace fossils are Gnathichnus pentax and Radulichnus inopinatus, produced by the grazing activity of echinoids and polyplacophorans upon algae and other microorganisms coating shell surfaces. Other bioerosion traces include polychaete dwellings (Caulostrepsis taeniola and Maeandropolydora sulcans), sponge boring systems (Entobia isp.), and rare bryozoan borings (Pinaceocladichnus isp.), predation structures (Oichnus simplex and repaired durophagous scars), and foraminiferal fixation pits (Centrichnus cf. eccentricus). The trace fossil assemblage records short−term bioerosion in shellgrounds in a moderate energy setting as evinced by the dominance of epigenic or shallow endogenic structures produced in most cases by “instantaneous” behaviors. The assemblage can be assigned to the Gnathichnus ichnofacies, and it contrasts with that found in Pliocene rocky shores in the same geographic area, which are examples of the Entobia ichnofacies. The Gnathichnusichnofacies is validated as an archetypal one and its recurrency demonstrated since the Jurassic. Entobia and Gnathichnus ichnofacies have to be used in the Mesozoic and Cenozoic as substitutes of the previously existing Trypanites ichnofacies, which is still valid in the Palaeozoic.
The trace fossil Spongeliomorpha iberica locally occurs in the Tortonian (Upper Miocene) marine strata of the Fortuna basin in southeastern Spain, and its excellent preservation state allows a reliable reconstruction of its main morphologic features. The burrow systems are branched (but not anastomosing), and they include numerous, short, blind tunnels. The burrow walls are strongly ornamented with bioglyphs displaying a rhomboidal pattern, consisting mostly of individual “Y”−shaped scratches. Smaller, secondary bioglyphs consist of sets of less incised transverse scratches. These features allow us to assign the ichnospecies to a decapod crustacean, most likely an alpheid or thalassinidean shrimp. The burrow apparently served as a refuge for the inhabitant, which fed upon microorganisms growing on the walls of the burrow by means of scraping the interior surfaces with the maxillipeds or other mouth parts. It is also likely that the shrimp used the multiple blind tunnels to store organic material (probably plant detritus) to be used for later consumption. The crustaceans colonized mud firmgrounds, which were formed by erosion during a rapid sea−level fall. Thus, the burrows occur in direct association with erosional regressive surfaces and therefore are good stratigraphic indicators of abrupt paleoenvironmental change.
This study describes the largest known Palaeozoic boring trace, Osprioneides kampto igen. et isp. nov., found within a stromatoporoid Densastroma pexisum from the Upper Visby Formation (lower Wenlock, Silurian) on the island of Gotland, Sweden. Differences between the physical properties of the stromatoporoid and the dense micritic infilling of the borings allowed the application of the CT−scan technology for the 2D and 3D−visualisation of this rare trace. The additional application of a stereoscopic technique on these CT images and movies enhances its value for unravelling spatial orientations. This non−destructive method has a great potential for future macroas well as microboring analyses. The trace maker, most likely a worm, infested the hosting colony post−mortem with up to 120 mm long borings measuring 5–17 mm in diameter. Smaller forms of Trypanites and Palaeosabella within the same stromatoporoid preferentially occur in the outer coenosteum and occasionally in abandoned borings of O. kampto. The stratigraphic position of O. kampto follows the “Great Ordovician Biodiversification Event” in time, and reflects the increase in diversity of boring species. Borings with penetration depths of 120 mm are, however, unique findings for the Palaeozoic and were not exceeded until some 260 million years later (Bajocian, Middle Jurassic) when the “Mesozoic Marine Revolution” led to convergent reinventions as a result of enhanced predation, grazing pressure, and ecospace competition.
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