The encrustation of fossil and recent sea-urchin tests: ecological and taphonomic significance

A comparison of fossil ( Echitwlampas sp. from the Lower Miocene Zogelsdorf Formation, Austria) and Recent ( Schizaster canaliferus from the northern Adriatic Sea) irregular sea-urchin tests shows that, upon their death, burrowing echinoids can serve as a substrate for a dense epigrowth. Size, shape, stable orientation, and surface residence-time were identified as key factors governing encrustation. The encrusters on fossil Echinolampas were bryozoans, serpulid polychaetes, barnacles, and coralline algae, while the recent material was initially encrusted by serpulids and hydrozoan colonies, and ultimately covered by the full range of sessile, hemi-sessile, and vagile species characterizing the benthic community in the Adriatic. In Echinolampas , epigrowth was more abundant on the lower (oral) surface; this specific distribution was echoed in S. canaliferus , where epigrowth started on the bottom side and grew upward. This indicates that the tests have a stable orientation and a surface residence-time long enough to allow intense encrustation. A taphonomic model is developed, and the role of encrustation on such special substrates for overall community structure is discussed. The Recent/fossil comparison provides new insights for both fields of study: the recent material indicates the role of soft-bodied faunas as well as the complexity of small-scaled ecological processes; the fossil material reflects many of the above phenomena and adds important taphonomic details on the fate of encrusted biogenic structures and on encruster growth patterns and distributions.     

Microbial encrustations from the Middle Oxfordian-earliest Kimmeridgian lithofacies in the Prebetic Zone (Betic Cordillera, southern Spain): characterization, distribution and controlling factors

Two main types of microbial encrustation were identified in Middle Oxfordian to lowermost Kimmeridgian deposits in the Prebetic Zone (southern Spain), showing existing relationships between skeletal content, fabric and morphology of these organosedimentary structures. Laminated planar and concentric encrustations relate to peloidal fabrics (mainly constituted of microbes = microbial laminated fabrics s. str. and microbial oncoids s. str.), as well as to dense microbial fabrics periodically colonized by encrusting foraminifera (microbial laminated fabrics with nubeculariids and microbial oncoids with nubeculariids). Sedimentation rates, substrate stability and grain size, as well as illumination, influenced microbial growth pattern as major controlling factors in low-energy conditions, and forced palaeogeographic and stratigraphic patterns of distribution. Significant encrustation was identified in terrigenous-poor lithofacies from the middle (Transversarium-Bifurcatus zones) to the outer (Transversarium-Bimammatum zones) shelf in the Prebetic Zone. Rare-to-absent encrustation characterized terrigenous-rich deposits (Bimammatum and Planula zones) in the area.     

Epizoan encrustation on Marsupites testudinarius – additional argument favoring an epifaunal mode of life of uintacrinoids?

Uintacrinoids (Uintacrinoidea Zittel) are among the best-known Late Cretaceous crinoids, but owing to their unusual morphology and widespread distribution their mode of life has become a subject of much discussion. Of several competing hypotheses, nektonic, pseudoplanktonic, hemipelagic, semi-infaunal and epibenthic lifestyles have been suggested. Recent study synthesizing and extending previous data has shown that these crinoids were epibenthic, holding their arms vertically for feeding. However, evidence supporting a rheophilic epibenthic model over an alternative rheophobic semi-infaunal model is still limited. Here we report epizoans, mostly represented by serpulids and bryozoans, encrusting thecal plates of Marsupites testudinarius from the Lägerdorf in Germany. Although a definitive interpretation whether recorded infestations occurred syn vivo or post mortem is not certain, it is remarkable that all epizoans (or their traces) are attached to the convex side (latera) of well-preserved isolated plates displaying no signs of reworking. Furthermore, a bryozoan colony crossing plate boundaries has been also found on the surface of a sub-articulated theca suggesting that it may have been colonised syn vivo. Recorded epibiotic associations, whether syn vivo or post-mortem, must have developed prior to burial of the specimens, above the surface of sea floor, and thus provide another argument against rheophobic semi-infaunal mode of life of uintacrinoids.     

Colonization by barnacles on fossil Clypeaster: an exceptional example of larval settlement

The presence of c. 1450 individuals of the balanid barnacle Balanus crenatus Bruguière encrusting the test of a clypeasteroid sea urchin from the Late Miocene of the Guadalquivir Basin (southwestern Spain) allows proposing a settlement pattern linked to the growth of the encrusting organism. The possible influence of dip angle was controlled by dividing the test into four concentric zones ranging from lowest margin to apex (0–15°, 15–30°, 30–50° and 0°). Contour diagrams were prepared to identify areas of highest barnacle density as well as size categories distribution in relationship to the pitch of the sea urchin test. The orientation of balanid tests was recorded and plotted on rose diagrams from 0° to 180°. Four size categories of barnacles were distinguished: (1) < 1 mm, (2) 1–2 mm, (3) 2–3 mm and (4) 3–4 mm; these correspond to a growth sequence ranging from post‐larval forms to juveniles. Two areas of maximum settlement density are situated on the posterior margin of the test, on aboral as well as oral surfaces. The aboral surface shows the maximum number of barnacles. Two groups of individuals are defined on the basis of their location, that is, those encrusting the posterior medium part of the urchin, and those located on the anterior half. The results suggest that larval settlement was initially controlled by the availability of free space and afterwards by an intensification effect. Orientation and dip of the test may have played a secondary role in the settlement of the larvae. Substrate colonization seems to have been closely related to the biostratinomic history of the sea urchin test and although several scenarios are possible, our data are congruent with a synchronous settlement of both surfaces (aboral and oral) by one spat or several.     

Taphonomic signatures on modern molluscs and corals from Red Sea coast,southern Saudi Arabia

Bioeroded gastropod, bivalve and coral specimens (n = 570) were collected from the Jazan area, Saudi Red Sea coast, from which 22 ichnospecies of 8 ichnogenera were identified and illustrated. These traces were produced by clionid sponges (Entobia geometrica, E. ovula, E. cf. goniodes, E. cretacea, E. laquea, E. cf. paradoxa and E. isp.), duraphagous drillers (Oichnus ovalis, O. paraboloides, O. simplex and O. isp.), endolithic bivalves (Gastrochaenolites cf. dijugus, G. lapidicus, G. torpedo and G. isp.), polychaete annelids (Caulostrepsis taeniola, C. isp., Maeandropolydora sulcans, M. isp. and ?Trypanites isp.), acorn barnacles (Rogerella isp.), and vermetid gastropods (Renichnus isp.). The seashells act as hard substrate for colonization by serpulid worm, bivalves, bryozoans, and barnacles. Ichnogenus Entobia was most abundant (56.1%), followed by Gastrochaenolites (25.4%), Caulostrepsis (5.3%), Trypanites (4.2%), Maeandropolydora (3.2%), Oichnus (2.8%), Renichnus (1.9%), and Rogerella (1.0%). Oichnus occurred on the thin-shelled and smooth molluscs, while most Gastrochaenolites borings were found in the larger and thicker seashells as a suitable substrate for the settlement of polychaetes, lithophages, naticids, mytilids, and vermetids. Presence of annelid traces among radial ribs and at the siphonal areas of bivalves is indicative of nutrient capturing from water flow during the lifetime of these bivalves, within a shallow, high energy marine environment, where disarticulation, fragmentation, and abrasion of the seashells were abundantly observed.     

Modelling crystal aggregation and deposition in the catheterised lower urinary tract

Urethral catheters often become encrusted with crystals of magnesium struvite and calcium phosphate. The encrustation can block the catheter, which can cause urine retention in the bladder and reflux into the kidneys. We develop a mathematical model to investigate crystal deposition on the catheter surface, modelling the bladder as a reservoir of fluid and the urethral catheter as a rigid channel. At a constant rate, fluid containing crystal particles of unit size enters the reservoir, and flows from the reservoir through the channel and out of the system. The crystal particles aggregate, which we model using Becker–Döring coagulation theory, and are advected through the channel, where they continue to aggregate and are deposited on the channel’s walls. Inhibitor particles also enter the reservoir, and can bind to the crystals, preventing further aggregation and deposition. The crystal concentrations are spatially homogeneous in the reservoir, whereas the channel concentrations vary spatially as a result of advection, diffusion and deposition. We investigate the effect of inhibitor particles on the amount of deposition. For all parameter values, we find that crystals deposit along the full length of the channel, with maximum deposition close to the channel’s entrance.     

Large gryphaeid oysters as habitats for numerous sclerobionts: a case study from the northern Red Sea

The shell of a living specimen of the Indo-Pacific gryphaeid giant oyster Hyotissa hyotis was colonized by numerous encrusting, boring, nestling and baffling taxa which show characteristic distribution patterns. On the upper valve, sponge-induced bioerosion predominates. On the lower valve intergrowth of chamid bivalves and thick encrusting associations—consisting mostly of squamariacean and corallinacean red algae, acervulinid foraminifera, and scleractinian corals—provides numerous microhabitats for nestling arcid and mytilid bivalves as well as for encrusting bryozoans and serpulids. Such differences between exposed and cryptic surfaces are typical for many marine hard substrata and result from the long-term stable position of the oyster on the seafloor. The cryptic habitats support a species assemblage of crustose algae and foraminifera that, on exposed surfaces, would occur in much deeper water.