Bivalve borings in Lower Jurassic Lithiotis fauna from northeastern Italy and its palaeoecological interpretation

Random shell sections of the Pliensbachian (Early Jurassic) larger bivalve Opisoma from columns within the Main Post Office building of Ferrara, northern Italy, have been discovered to bear neat clavate-shape boreholes. These boreholes belong to the ichnogenus Gastrochaenolites Leymerie and represent bivalve borings. Opisoma is a subordinate component of the Lithiotis fauna characterised by aberrant shells thriving in tropical lagoonal settings which were widespread throughout the Tethyan and Panthalassa coasts. Although the Lithiotis fauna is well known in the palaeontological literature, no bivalve boring have been so far been formally described. The uniqueness of the morphology, size and substrate of these borings merits the designation of the new species Gastrochaenolites messisbugi ichnosp. nov. which thereby represents the first ichnospecies described from this fauna. The morphology of the boreholes and the included bivalves allows the boring activity to be ascribed to a mytilid bivalve. Palaeoecological and taphonomic analyses allowed the presence of the boreholes to be correlated to the Opisoma mode of life (epifaunal, free-living form) as well as to generally low sedimentation rates and seasonal mesotrophic conditions during an overall oligotrophic regime.

http://zoobank.org/urn:lsid:zoobank.org:act:CCF77B32-D459-4305-BC86-93F228852E50     

Borings in mobile clasts from Eocene conglomerates of Northern Dalmatia (Coastal Dinarides, Croatia)

Summary Bored clasts occur in Eocene conglomerates deposited in the upper shoreface and beachface settings of the Dinaric foreland basin. The trace fossil assemblage consists ofGastrochaenolites, Trypanites, and possibly some other ichnotaxa and may be compared to theTrypanites Ichnofacies. The preservation characteristics of the borings reflect many stages of colonisation/boring and abrasion. The removal of shells of the boring bivalves, the different depths of the abrasional truncation of borings, and the predominant preservation of the largest excavations (Gastrochaenolites) in the ichnocoenosis are related to repeated phases of abrasion, caused by the mobility of clasts. Coastal gravel is a specific variant of hard substrates, whose mobility controls the colonisation of borers, the type of assemblage and its preservation potential.     

Bioerosion in the Miocene Reefs of the northwest Red Sea,Egypt

Macroborings provide detailed information on the bioerosion, accretion and palaeoenvironment of both modern and fossil reefs. Dolomitized reefal carbonates in the Um Mahara Formation exhibit an outstanding example of spatially distributed, well‐preserved bioerosion structures in tropical to subtropical syn‐rift Miocene reefs. Ten ichnospecies belonging to five ichnogenera are identified; three belonging to the bivalve‐boring ichnogenus Gastrochaenolites, three attributed to the sponge‐boring ichnogenus Entobia, and four ichnospecies assigned to three worm‐boring ichnogenera Trypanites, Maeandropolydora and Caulostrepsis. The distribution of the reported borings is strongly linked to the palaeo‐reef zones. Two distinctive ichnological boring assemblages are recognized. The Gastrochaenolites‐dominated assemblage reflects shallower‐marine conditions, under water depths of a few metres, mostly in back‐reef to patch‐reef zones of a back‐reef lagoon. The Entobia‐dominated assemblage signifies relatively deeper marine conditions, mostly in reef core of the fringing Miocene reefs. These ichnological assemblages are attributed herein to the Entobia sub‐ichnofacies of the Trypanites ichnofacies. This ichnofacies indicates boring in hard carbonate substrates (such as corals, rhodoliths, carbonate cements and hardgrounds) during periods of non‐sedimentation or reduced sediment input.     

Ichnofacies and microbial build-ups on Late Miocene rocky shores from Menorca (Balearic Islands), Spain

Angular unconformites between Jurassic and Miocene strata are exposed in the sea cliffs of Cala Cigonya on the northwest coast of Menorca in the Balearic Islands of Spain. The geological discontinuities represent rocky shores on opposite sides of a former headland with 15 m of topographic relief. On the east flank, Jurassic dolomite is overlain by Upper Miocene (Tortonian to Messinian) breccia and laminated limestone. Here, a partially exhumed dolomite surface records Miocene bivalve borings of the ichnospecies Gastrochaenolites torpedo and G. lapidicus that achieved a density of >1,000 borings/m². Other associated traces include sponge borings (Entobia isp.) and polychaete borings (Caulostrepsis isp.). A breccia deposit 0.8 m thick was derived from the underlying dolomite and angular clasts still retain evidence of bivalve borings. Above follows a succession of laminated limestone beds more than 5 m thick, including some levels with dome-shaped stromatolites and other horizons with reworked dolomite clasts. Thin-section analysis of the laminated limestone reveals dark and light couplets 0.2 mm thick consistent with microbial origins. In contrast, the west flank was buried by coarse sandstone and laminated sediments. Here, dwelling structures of regular echinoids (Circolites kotoncensis) are the dominant traces preserved on the dolomite surface, reaching a maximum density of 66 borings/m². Associated borings include Entobia geometrica as well as rare traces of Gastrochaenolites isp. and Trypanites isp. Notable for the absence of a basal Miocene breccia, the west flank is interpreted as a sheltered rocky shore coeval with an exposed rocky shore on the east flank. Today, heavy surf on the north coast of Menorca is related to the Tramontana winds that blow out of Spain during winter months. Similar atmospheric circulation patterns must have prevailed during the Late Miocene, but the replacement of ichnofacies by microbial build-ups resulted from increased salinity during the Messinian crisis.     

Recent borings in limestone cobbles from Marloes Bay, southwest Wales

Limestone clasts from the beach at Marloes Sands, southwest Wales, contain slender, straight to sinuous borings cross-cut by younger, clavate borings. The former were probably produced by sipunculids or polychaetes; the latter preserve shells of the boring bivalve Gastrochaena dubia (Pennant). Unusually, the calcareous linings of the clavate bivalve borings extend into many of the slender worm borings. Such linings are considered part of the hard parts of the producing bivalve, but the chance association of the two morphologies of borings has led to the lining becoming intimately associated with both of them. The modified linings of the bivalve borings have a similar morphology to the crypt of certain clavagellid bivalves, perhaps presenting an analogue for the morphology of a pre-clavagellid, boring ancestor.     

Site selection and behavior of sponge and bivalve borers in shells of the cretaceous oysters exogyra cancellata and pycnodonte mutabilis from delaware,U.S.A

In shells of the oysters Exogyra cancellata and Pycnodonte mutabilis from the Mount Laurel and Marshalltown Formations (Campanian‐Maestrichtian), three‐quarters of all valves bear sponge borings (Entobia isp.) borings and 30% have borings of a lithophagid bivalve (Gastrochaenolites isp.). Non‐random distributions of these euendoliths, documented in this paper, may in part be accounted for by differential survival of sponge and lithophagid larvae and spat in varying circumstances. In addition, exterior shell architectures and post‐mortem orientations of shells are inferred to have prompted active geophobic (antigravity), rugophilic (groove‐seeking), and rheophilic (current‐seeking) behavior that enhanced survivorship of the settling larvae.     

Rocky-shore unconformities marking the base of Badenian (Middle Miocene) transgressions on Mt. Medvednica basement (North Croatian Basin,Central Paratethys)

Badenian (Middle Miocene) transgressive deepening-upward successions located in the NE part of Mt. Medvednica (North Croatian Basin, Pannonian Basin System) unconformably overlie Mesozoic basement. Triassic and Upper Cretaceous limestone pebbles, cobbles, and boulders of the Badenian basal conglomerates display abundant in situ bivalve borings of Gastrochaenolites and sponge borings of Entobia. This Gastrochaenolites-Entobia ichnoassemblage is related to the Entobia subichnofacies of the Trypanites ichnofacies, characterizing littoral rocky-shore environments (wave-cut platforms and marine transgressive surfaces with a low or null rate of sedimentation). Gastrochaenolites torpedo, Gastrochaenolites lapidicus, and Entobia recorded in Badenian basal conglomerates (compared with modern Northern Adriatic rocky-shore environments), enabled more precise palaeoenvironmental interpretations. The occurrence of G. torpedo (produced by lithophaginid bivalves) on all sides of individual limestone lithoclasts in the Gornje Ore?je basal conglomerate, coupled with truncation of the formation (possibly indicating multiphase colonization), reflect gravel transport, roll-over, overturning and erosion by wave action in high-energy rocky-shore settings. Gornje Psarjevo-2 basal conglomerate boulders were probably not subjected to significant movement and abrasion, as suggested by good preservation of both G. lapidicus (potentially produced by gastrochaenid bivalves), associated G. torpedo, as well as abundant shallow Entobia borings. The Badenian Gastrochaenolites-Entobia ichnoassemblage also could be the result of a composite development. However, direct cross-cutting relationships between G. torpedo and G. lapidicus and/or Entobia were rarely observed. In addition, Badenian boring tracemakers might have coexisted at the same water depth. Northeast Mt. Medvednica Badenian successions probably formed during different Central Paratethys transgressive pulses (NN5 and NN6 Zones). However, exact timing of Badenian transgressions, stratigraphic correlations and tectono-eustatic implications are unresolved, due to sparsely integrated biostratigraphic and high-precision geochronological studies of Early–Middle Miocene North Croatian Basin deposits and due to the absence of a uniform biostratigraphic zonation and regional chronostratigraphic division of Central Paratethys.     

Determination of a Late Miocene rocky palaeoshore by bioerosion trace fossils from the Bozcaada Island, Çanakkale,Turkey

Bioerosion is a common process in hard substrates. This study introduces an example from the rocky palaeoshore cropping out at a sea cliff on the Bozcaada Island. It includes bioerosion trace fossils preserved in limestone boulders of the shallow marine and lacustrine Alcitepe Formation of Late Miocene age. The ichnotaxa include borings produced by duraphagous drillers (Oichnus isp.), phonorids (cf. Conchotrema isp.), clionid sponges (Entobia cf. goniodes, Entobia geometrica, Entobia laquea, Entobia ovula, E. cf. solaris, Entobia isp.), endolithic bivalves (Gastrochaenolites torpedo, Gastrochaenolites lapidicus, Gastrochaenolites isp., Phrixichnus isp.), polychaete annelids (Maeandropolydora isp., Maeandropolydora sulcans, Maeandropolydora decipiens, Caulostrepsis taeniola, Caulostrepsis isp.), echinoids (cf. Circolites isp.) and spinculid worms (cf. Trypanites isp.). Barnacles are also common as encrusters. The borings can be ascribed to the Gastrochaenolites-Entobia assemblage, which is typical of Neogene rocky-shores. They belong to the Entobia ichnofacies indicating various conditions of light, energy, and depth. Therefore they can reveal environmental changes and play an important role in forming palaeo-rocky shores and wave-cut platforms during marine trangressive events.     

Epi- and endobiontic organisms on Late Jurassic crinoid columns from the Negev Desert, Israel: Implications for co-evolution

Columns of the articulate crinoids Millericrinus and Apiocrinites from the Upper Jurassic (Upper Callovian) Zohar and Matmor formations of the Negev Desert of Israel display abundant encrusting organisms of about ten species, as well as diverse trace fossils produced by endobionts. Pluricolumnals were colonized by epi- and endobiontic organisms both during life and post-mortem. Skeletonized encrusting organisms include abundant ostreid bivalves (which evidently colonized both live and dead crinoid columnals), two types of serpulid worms, encrusting foraminifera, three species of bryozoans, and small encrusting sclerosponges. Several types of borings are present: Trypanites (possibly produced by sipunculids), Gastrochaenolites (crypts of boring lithophagid bivalves), elliptical barnacle? borings, and channel-like annelid? borings. In addition, approximately 16% of the pluricolumnals display circular parabolic embedment pits assignable to the ichnogenus Tremichnus. They are associated with substantial deformation of the containing columnals and were probably the work of host-specific ectoparasitic organisms. Discovery of Tremichnus on Jurassic crinoids extends the range of this trace by almost 100 million years, providing evidence for one of the longest-ranging host-parasite interactions documented thus far (over 200 million years). The relationship of epibionts to the Jurassic crinoids thus ranged from simple utilization of dead hard substrate to probable opportunistic commensalism in forms that colonized the live upright stems, as in some oysters, through host-specific parasitism in the case of Tremichnus.     

Bioerosional structures and pseudoborings from Late Jurassic and Late Cretaceous-Paleocene shallow-water carbonates (Northern Calcareous Alps, Austria and SE France) with special reference to cryptobiotic foraminifera

Examples of bioerosional processes (boring patterns) are described from shallow-water limestones of the Late Jurassic Plassen Carbonate Platform (PCP) and the Late Cretaceous to Paleocene Gosau Group of the Northern Calcareous Alps, Austria. Some micro-/macro-borings can be related to distinct ichnotaxa, others are classified in open nomenclature. In the Alpine Late Jurassic, bioerosional structures recorded from clasts in mass-flows allow palaeogeographical conclusions concerning the source areas. In particular, these are borings of the Trypanites-ichnofacies detected from clasts (Barmstein limestones) of the PCP or special type of bored ooids of unknown source areas or restricted autochthonous occurrences. In the Lower Gosau Subgroup, Gastrochaenolites macroborings occur in mobile carbonate clast substrates of shore zone deposits (“Untersberg Marmor”). Different types of borings are recorded from rudist shells and coral skeleton, some of which are referable to the ichnotaxon Entobia produced by endolithic sponges. In the present study, special attention is paid to the occurrences of the cryptobiotic foraminifera Troglotella incrustans Wernli and Fookes in the Late Jurassic and Tauchella endolithica Cherchi and Schroeder in the Late Cretaceous. The latter is so far only known to be from the Early Cenomanian of France and is reported here for the first time from the Late Turonian-Early Coniacian stratigraphic interval where it was found in turbulent carbonate deposits within borings penetrating bivalve shells or coralline algae. The records of cryptobiotic foraminifera from the Northern Calcareous Alps are supplemented by a single finding from the Middle Cenomanian of SE France. A palaeoenvironmental interpretation of the occurrences of the cryptobiotic foraminifera is provided.     

Bioerosive structures from Miocene marine mobile‐substrate communities in southern Spain,and description of a new sponge boring

Abstract: Neogene palaeoshore sediments are abundantly represented along the Mediterranean coast of Iberia. An outcrop north of the Sierra Tejeda, named La Resinera, exposes concentrations of pebbles and boulders of marble, comprising an upper Miocene marine beach deposit. The high diversity of bioerosion trace fossils present in these boulders includes structures produced by polychaete annelids, demosponges, echinoids and endolithic bivalves, which indicate a shallow shoreface environment. The ichnotaxa represented are Maeandropolydora sulcans, Caulostrepsis taeniola, Entobia geometrica, Entobia ovula, Circolites kotoncensis, Gastrochaenolites torpedo, Gastrochaenolites lapidicus, Gastrochaenolites ornatus and Gastrochaenolites turbinatus. The borings are Tortonian (late Miocene) in age. Also present, and particularly abundant, are large sponge borings that have a single chamber from which radiating canals emerge. This trace fossil is designated as Entobia resinensis isp. nov.     

A Distinctive Bioglyph and its Producer: Recent Gastrochaenolites Leymerie in a Peat Pebble,North Sea Coast of The Netherlands

A pebble of Quaternary peat collected from the Dutch coast north-northeast of Zandvoort, Noord Holland, preserves a recent boring, Gastrochaenolites isp. cf. G. lapidicus. This is geniculated and retains a distinctive, corrugated bioglyph. The probable producing bivalve was the pholad Barnea candida (Linné), known as the white piddock, or Petricola pholadiformis Lamarck, known as the American piddock, identified by beachcombing for boring shells. But these form a minute numerical fraction of a modern shelly death assemblage dominated by burrowing bivalves; an analogous approach with the fossil record is less likely to succeed.     

An Intersection in Time and Space: Significance of Modern Invertebrate Borings in Upper Cretaceous Echinoids

Reworked fossils may contribute unique data to ichnology, stratigraphy, and paleoecology. Reworked Upper Cretaceous echinoids are found on Ocean Isle Beach, North Carolina, United States. Tests of Hardouinia sp. cf. H. mortonis were intensely bored by clionaid sponges (Entobia) and bivalves (Gastrochaenolites), with rare polychaete annelids (Caulostrepsis). Evidence for a high-energy environment in the Late Cretaceous is provided by the sandstone infill and a geopetal infill. Hardouinia were bored on all surfaces, largely lack surface detail and have been corraded, exposing the internal structure of some borings, indicating that these specimens were tumbled in a modern, high energy marine environment. Borers showed substrate preferences: Entobia is largely limited to the test, but do penetrate the sandstone infill in some specimens; Caulostrepsis mainly infested the crystalline calcite of the echinoid test; and Gastrochaenolites penetrated both tests and lithified sandstone infill. This Entobia-Gastrochaenolites assemblage in these echinoids differs from the Entobia-Caulostrepsis assemblage recognized from the approximately coeval, but spatially distant, tests of Upper Cretaceous Echinocorys ex gr. scutata found reworked on the North Sea coast of Norfolk, England. Unlike the Entobia-Gastrochaenolites association of North Carolina, the boring association in Norfolk is between Entobia and Caulostrepsis, which are found in both tests and chalk infill. Thus, the lithology of the infill is an important factor in determining these differences.     

Holes in Bones: Ichnotaxonomy of Bone Borings

Bone is a substrate for bioerosion at equal rank with xylic and lithic substrates. Accordingly, borings in bone have to be identified in an analogous way to other ichnogenera coined for one type of substrate. In due course, the new ichnogenera Osteichnus n. igen. and Clavichnus n. igen. are established within the new ichnofamily Osteichnidae. Gastrochaenolites and Trypanites are here restricted to lithic substrates, and Asthenopodichnium only occurs in xylic substrates. Only with this approach, ichnotaxobases of trace fossils in bone are identical to those in other hard substrates. Cuniculichnus variabilis n. igen. n. isp. is introduced for variably shaped pits to tunnels bored into bone by beetle (arguably dermestid) larvae; its ethological character is close to a pupichnion.     

Paleontological evidence of a brief global sea-level event during the last interglacial

A gently undulating to flat erosion surface with shallow-water borings and burrows is present in the midst of a Sangamonian (Eemian; marine oxygen isotope substage 5e) reefal facies on the islands of San Salvador and Great Inagua, Bahamas. Precise U/Th dating of corals above and below this surface show that it formed around 125-124 ka, and that the sea-level regressive-transgressive cycle which produced it lasted for 1500 years or less. The surface occurs on entirely carbonate rocks and has a low relief punctuated by erosional channels and karstic caves formed during the sea-level lowstand. A terra rossa paleosol, developed during that lowstand, partially fills a set of large lithophagid bivalve borings ( Gastrochaenolites torpedo ), showing that they were excavated during the regression. Rhizomorphs formed by plant roots occur on the erosion surface at Great Inagua. Extensive boring of the upward-facing surfaces occurred during the ensuing transgression, including a smaller G. torpedo and a clionid sponge boring ( Entobia ovula ). The bored surface is encrusted by a variety of shallow-water corals and, eventually, the re-established bank-barrier coral reefs. A sparse assemblage of serpulid worm and vermicularid gastropod tubes encrusted the channel and cave walls. Robust Ophiomorpha burrow systems occur within pockets of sediment in the coral facies both below and above the erosion surface. The channels and caves are filled with transgressive calcarenitic sediments in which occur numerous Ophiomorpha and Skolithos burrows. The ichnofossils on, below, and above this erosion surface are prominent indicators of a short-lived but significant global sea-level event.     

Bivalve Wood Borings of the Ichnogenus Teredolites Leymerie from the Bohemian Cretaceous Basin (Upper Cretaceous,Czech Republic)

Finds of fossil wood with bivalve wood borings (Teredolites clavatus and T. longissimus) occur in various facies and presumed sedimentary settings of the platform, shallow-marine Bohemian Crectaceous Basin. The basin comprises areas with sandy-dominated sediments, with marl and clay-dominated sediments, areas with predominat sandy-marly rocks, and finally areas dominated by calcareous nearshore sediments. Teredolites clavatus is common in fossil wood of sandstones, originating in beach or deltaic settings; marl and clay-dominated rock frequently bear wood fragments densely bored by Teredolites longissimus. When accompanied by evidence of marine environments as body fossils, glauconite or typical trace fossils, most of the wood fragments are bored. The presence/absence of borings in wood fragments can be considered the most reliable and easily useable criterion of distinction of marine settings in sandy sediments of the margin of the Bohemian Cretaceous Basin.     

Microboring in a Freshwater Fluvial Unionid Bivalve Substrate

Samples of the unionid bivalve Elliptio complanata were collected from the channel of the freshwater Saint John River, from Fredericton, New Brunswick, Canada. Scanning electron microscopy imaging of prepared shell samples revealed an assemblage of microborings. No borings are noted on the periostracum or prismatic shell layers. Boring structures are instead confined to the underlying nacreous aragonitic shell material, together with its associated organic conchiolin layers. Three main styles of boring are encountered, encompassing both predominantly surficial structures and penetrative tubular borings. Surficial structures are represented by a polygonal network on an exposed conchiolin shell layer. The penetrative borings take two forms, one being simple unbranched tubes, steeply aligned (perpendicular to the shell surface) and traversing the full thickness of the nacreous shell layer. The other penetrative boring style, again occurring within the nacreous layer, comprises a complex irregular network of randomly oriented rarely branching tubular borings. Borings generally display diameters of micron scale. Biofilm and extracellular polymeric substances, with bacterial, diatomaceous and filamentous components are also observed, often displaying a close association with both the borings and the conchiolin layers within the shell. The formation of the borings may be attributed to cyanobacteria, cyanophyte or fungal progenitors.     

Bored Bivalves in Upper Triassic (Norian) Event Beds,Northeastern British Columbia,Canada

Skeletobionts are important components of most shallow marine ecosystems. Prior to the fossils reported herein, evidence of skeletobionts was absent from Upper Triassic successions on the northwestern margin of Pangaea. The boring Talpina ramosa is reported from bivalve body fossils from the Upper Triassic (Lower Norian) lower Pardonet Formation at Pink Mountain in northeastern British Columbia. This Ichnotaxon penetrates through both the outer and inner surface of articulated and disarticulated bivalve shells preserved within sharp-based event beds. The occurrence of these trace fossils underscores the paucity of borings, bioerosional structures, and encrusting taxa from Triassic successions in the western Pangaean realm. Due to erosional removal of shallow water strata by a post-Triassic unconformity, these event beds provide the only available information regarding the ecological health of Late Triassic depositional systems in the study area.     

Bioerosion of gastropod shells: with emphasis on effects of coralline algal cover and shell microstructure

Organisms boring into fifty nine species of gastropod shells on reefs around Guam were the bryozoan Penetrantia clionoides; the acrothoracian barnacles Cryptophialus coronorphorus, Cryptophialus zulloi and Lithoglyptis mitis; the foraminifer Cymbaloporella tabellaeformis, the polydorid Polydora sp. and seven species of clionid sponge. Evidence that crustose coralline algae interfere with settlement of larvae of acrothoracian barnacles, clionid sponges, and boring polychaetes came from two sources: (1) low intensity of boring in limpet shells, a potentially penetrable substrate that remains largely free of borings by virtue of becoming fully covered with coralline algae at a young age and (2) the extremely low levels of boring in the algal ridge, a massive area of carbonate almost entirely covered by a layer of living crustose corallines. There was a strong negative correlation between microstructural hardness and infestation by acrothoracian barnacles and no correlation in the case of the other borers. It is suggested that this points to a mechanical rather than a chemical method of boring by the barnacles. The periostracum, a layer of organic material reputedly a natural inhibitor of boring organisms, was bored by acrothoracican barnacles and by the bryozoan. The intensity of acrothoracican borings is shown to have no correlation with the length of the gastropod shell.