Abstract:Abundant Skolithos burrows are here described from a possible regressive event bed at Ohesaare cliff (Pridoli), Saaremaa, Estonia. The vertical, cylindrical burrows are identified as Skolithos rather than Trypanites because they intercept and bypass rather than cut bioclasts in the limestone matrix. The absence of encrustation on the upper bedding surface also is evidence that these traces are soft-sediment burrows rather than hardground borings. We interpret this intensive bioturbation by Skolithos-producing … Show more
“…Similarly, a taxonomic polarity of epibionts has been reported from the reef stromatoporoids from the Ludlow of Gotland (SEGARS & LIDDELL, 1988). Anticalyptraea has previously been reported from cryptic surfaces under the late Silurian hardground from Ohesaare, Saaremaa (VINN & WILSON, 2010a). Cryptic surfaces in the Silurian were similar to the Ordovician, being mostly populated by the bryozoans, and cornulitids may also have been locally important (KERSHAW, 1980;TAYLOR & WIL-SON, 2003).…”
Section: Discussionmentioning
confidence: 60%
“…Encrustation patterns and bioerosion is relatively well known for western Baltica, especially for Gotland, Sweden (KERSHAW, 1980;NIELD, 1984;BEUCK et al, 2008). However, little published data on sclerobionts are available from the Silurian of eastern Baltica (KALJO, 1970;VINN & WILSON, 2010a, 2010b.…”
A shallow shelf carbonate platform (pelletal limestone facies) stromatoporoid association from the late Sheinwoodian of Saaremaa (Baltica) contains a diverse assemblage of sclerobionts (both epi-and endobionts). The studied stromatoporoids vary from low domical to extended domical shapes. Cornulites sp. aff. C. stromatoporoides, Conchicolites sp., Anticalyptraea calyptrata, microconchids, tabulate (Aulopora sp., Catenipora sp. and favositids) and rugose corals, sheet-like trepostome bryozoans, and discoidal crinoid holdfasts encrust the stromatoporoids. The dominant sclerozoans were tabulate and rugose corals, which is significantly different from several analogous Silurian sclerobiont communities. There may have been taxonomic polarity between an upper surface and a cryptic sclerozoan community. Bioerosion occurs as macroborings in 45.5 % of studied (N=22)
“…Similarly, a taxonomic polarity of epibionts has been reported from the reef stromatoporoids from the Ludlow of Gotland (SEGARS & LIDDELL, 1988). Anticalyptraea has previously been reported from cryptic surfaces under the late Silurian hardground from Ohesaare, Saaremaa (VINN & WILSON, 2010a). Cryptic surfaces in the Silurian were similar to the Ordovician, being mostly populated by the bryozoans, and cornulitids may also have been locally important (KERSHAW, 1980;TAYLOR & WIL-SON, 2003).…”
Section: Discussionmentioning
confidence: 60%
“…Encrustation patterns and bioerosion is relatively well known for western Baltica, especially for Gotland, Sweden (KERSHAW, 1980;NIELD, 1984;BEUCK et al, 2008). However, little published data on sclerobionts are available from the Silurian of eastern Baltica (KALJO, 1970;VINN & WILSON, 2010a, 2010b.…”
A shallow shelf carbonate platform (pelletal limestone facies) stromatoporoid association from the late Sheinwoodian of Saaremaa (Baltica) contains a diverse assemblage of sclerobionts (both epi-and endobionts). The studied stromatoporoids vary from low domical to extended domical shapes. Cornulites sp. aff. C. stromatoporoides, Conchicolites sp., Anticalyptraea calyptrata, microconchids, tabulate (Aulopora sp., Catenipora sp. and favositids) and rugose corals, sheet-like trepostome bryozoans, and discoidal crinoid holdfasts encrust the stromatoporoids. The dominant sclerozoans were tabulate and rugose corals, which is significantly different from several analogous Silurian sclerobiont communities. There may have been taxonomic polarity between an upper surface and a cryptic sclerozoan community. Bioerosion occurs as macroborings in 45.5 % of studied (N=22)
“…Thus, the vesicular shell structure of Anticalyptraea could be a protective morphology. In addition to thick vesicular walls, Anticalyptraea has reported to have some preference for the cryptic surfaces when associated with the hardgrounds in Pridoli of Saaremaa that can indicate predation pressure (VINN & WILSON, 2010b). The latest known Anticalyptraea-like fossils belong to Streptindytes (Middle Devonian to Carboniferous), which lived embedded in the host coral skeleton.…”
Section: Discussionmentioning
confidence: 99%
“…It belongs to encrusting tentaculitoid tubeworms and is closely related to cornulitids, microconchids and tentaculitids (VINN & ISAKAR, 2007;VINN, 2010). Anticalyptraea occurs as an encruster on various shelly fossils, such as brachiopods, stromatoporids, corals, but also on hardgrounds (VINN & WILSON, 2010b). The aims of this paper are: 1) to describe in detail the shell repairs in the encrusting tentaculitoid tubeworm Anticalyptraea for the first time; 2) to assess how often Anticalyptraea was attacked by predators in the late Silurian; 3) to describe shell repair mechanisms in Anticalyptraea; 4) to find correlations between shell repair rate and size of Anticalyptraea specimens; and 5) to discuss possible antipredatory adaptations in Anticalyptraea morphology and behavior.…”
Shell repair is common in the late Silurian (Pridoli) encrusting tentaculitoid tubeworm Anticalyptraea calyptrata from Saaremaa, Estonia (Baltica), and is interpreted here as a result of failed predation. A. calyptrata has a shell repair frequency of 29 % (individuals with scars) with 17 specimens. There is probably an antipredatory adaptation, i.e. extremely thick vesicular walls, in the morphology of Silurian Anticalyptraea. The morphological and ecological evolution of Anticalyptraea could thus have been partially driven by predation.Key Words: Predation; shell repair; Tentaculita; Anticalyptraea; Pridoli; Silurian; Estonia. Résumé : Réparation de la coquille chez Anticalyptraea (Tentaculita) dans le Silurien supé-rieur (Pridoli) du bouclier balte (Baltica).-La réparation de coquilles est habituelle chez Anticalyptraea calyptrata, un vers tentaculitoïde encroûtant du Silurien supérieur (Pridoli) à Saaremaa, Estonie (bouclier balte), et est interprétée ici comme la conséquence d'une prédation qui aurait échoué. A. calyptrata a une fréquence de réparation de la coquille de 29% (individus présentant des cicatrices) pour 17 spécimens. Ceci est probablement une adaptation contre la prédation, c'est-à-dire la présence de parois vésiculaires et très épaisses, présentes dans la morphologie de l'Anticalyptraea du Silurien. L'évolution morphologique et écologique d'Anticalyptraea pourrait donc pour partie avoir été provoquée par la prédation.
“…Diverse and rich benthic fauna and intense bioturbations in the Ohesaare section indicate shallow nearshore environments. The presence of such trace fossils as Cruziana and Skolithos has led to interpretations that this part of the basin presumably had high hydrodynamic energy (Vinn & Wilson 2013;Vinn 2014). In this work we present results of the first REE analyses from fish microremains of this important early vertebrate site and the first quantitative interpretations of the REE data record as a proxy to palaeoredox conditions and palaeoenvironment.…”
Rare earth element (REE) compositions of Nostolepis sp. scales, spines, plates and tesserae from Ohesaare bone beds were measured by in situ microsampling using laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). The obtained REE concentrations, normalized to Post-Archean Australian Shale concentrations, were evaluated using basic geochemical calculations and quantifications. The REE compositions were nearly identical across all the morphotypes and histologies of Nostolepis microremains, showing flat REE patterns with slight depletion in heavy REEs. There was no visible enrichment in middle REEs, indicating good geochemical preservation of bioapatite and absence of any pronounced fractionated REE incorporation during later stages of diagenesis. The shale-normalized (La/Yb) SN and (La/Sm) SN REE ratio compilations indicated adsorption as the dominating REE uptake mechanism across all datapoints. The absence of well-defined Ce anomaly suggested oxic palaeoseawater conditions, which agrees with the existing interpretations of the Ohesaare sequence as high-energy shoal and regressive open ocean sedimentary environments.
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