Abstract:Ippolitov, A.P., Vinn, O., Kupriyanova, E.K. and Jäger, M. 2014. Written in stone: history of serpulid polychaetes through time. Memoirs of Museum Victoria 71: 123-159.Although the fossil record of annelids in general is poor, calcareous tube-building Serpulidae are a notable exception. The "stumbling block" of understanding the serpulid fossil record is obtaining reliable taxonomic interpretations of fossil tubes based on morphology. Luckily, serpulid tubes demonstrate high variety of ultrastructures and nonu… Show more
“…While there has been some confusion as to whether chaetopterid tubes contain chitin (Barnes 1964;Ippolitov et al 2014;Parry et al 2014), our FTIR (Fig. 24) and py-GC-MS (Supplementary File 1, Table S7) results from four chaetopterid genera suggest that they do not, as three major chitin marker pyrolysis products that were commonly observed in siboglinid tubes were absent from the tubes of chaetopterids.…”
Section: Discussionmentioning
confidence: 78%
“…As annelid dwelling tubes are not joined to the annelid body and the adaptive evolution of tubes is considered independent to that of soft tissues (Ippolitov et al 2014), tubes have generally been considered to have limited utility in taxonomy. However, there are recognized characters of fossil tubes, such as tube wall structure in fossil serpulid tubes from seeps (Vinn et al 2012), that can enable taxonomic designation.…”
Section: Tube Morphologymentioning
confidence: 99%
“…sediment grains), and tubes comprised purely of an organic secretion. Calcareous tubes are almost exclusively confined to the family Serpulidae, but single extant sabellid and cirratulid genera also produce calcareous tubes (Ippolitov et al 2014). Calcareous tubes can be formed of either calcite or aragonite, or of both minerals, and may also exhibit distinct crystal microstructures (Vinn et al 2008).…”
Section: Introductionmentioning
confidence: 99%
“…However, the dwelling tubes that many annelids create are often more robust structures that have a greater likelihood of becoming preserved as fossils (Ippolitov et al 2014;Georgieva et al 2015a), and especially so within vents and seeps where rapid mineral precipitation often favours fossilization.…”
One of the main limitations to understanding the evolutionary history of hydrothermal vent and cold seep communities is the identification of tube fossils from ancient deposits. Tube-dwelling annelids are some of the most conspicuous inhabitants of modern vent and seep ecosystems, and ancient vent and seep tubular fossils are usually considered to have been made by annelids. However, the taxonomic affinities of many tube fossils from vents and seeps are contentious, or have remained largely undetermined due to difficulties in identification. In this study, we make a detailed chemical (Fourier-transform infrared spectroscopy and pyrolysis gas-chromatography mass-spectrometry) and morphological assessment of modern annelid tubes from six families, and fossil tubes (seven tube types from the Cenozoic, 12 Mesozoic and four Palaeozoic) from hydrothermal vent and cold seep environments. Characters identified from these investigations were used to explore for the first time the systematics of ancient vent and seep tubes within a cladistic framework. Results reveal details of the compositions and ultrastructures of modern tubes, and also suggest that two types of tubes from ancient vent localities were made by the annelid family Siboglinidae, which often dominates modern vents and seeps. Our results also highlight that several vent and seep tube fossils formerly thought to have been made by annelids cannot be assigned an annelid affiliation with any certainty. The findings overall improve the level of quality control with regard to interpretations of fossil tubes, and, most importantly, suggest that siboglinids likely occupied Mesozoic vents and seeps, greatly increasing the minimum age of the clade relative to earlier molecular estimates.
“…While there has been some confusion as to whether chaetopterid tubes contain chitin (Barnes 1964;Ippolitov et al 2014;Parry et al 2014), our FTIR (Fig. 24) and py-GC-MS (Supplementary File 1, Table S7) results from four chaetopterid genera suggest that they do not, as three major chitin marker pyrolysis products that were commonly observed in siboglinid tubes were absent from the tubes of chaetopterids.…”
Section: Discussionmentioning
confidence: 78%
“…As annelid dwelling tubes are not joined to the annelid body and the adaptive evolution of tubes is considered independent to that of soft tissues (Ippolitov et al 2014), tubes have generally been considered to have limited utility in taxonomy. However, there are recognized characters of fossil tubes, such as tube wall structure in fossil serpulid tubes from seeps (Vinn et al 2012), that can enable taxonomic designation.…”
Section: Tube Morphologymentioning
confidence: 99%
“…sediment grains), and tubes comprised purely of an organic secretion. Calcareous tubes are almost exclusively confined to the family Serpulidae, but single extant sabellid and cirratulid genera also produce calcareous tubes (Ippolitov et al 2014). Calcareous tubes can be formed of either calcite or aragonite, or of both minerals, and may also exhibit distinct crystal microstructures (Vinn et al 2008).…”
Section: Introductionmentioning
confidence: 99%
“…However, the dwelling tubes that many annelids create are often more robust structures that have a greater likelihood of becoming preserved as fossils (Ippolitov et al 2014;Georgieva et al 2015a), and especially so within vents and seeps where rapid mineral precipitation often favours fossilization.…”
One of the main limitations to understanding the evolutionary history of hydrothermal vent and cold seep communities is the identification of tube fossils from ancient deposits. Tube-dwelling annelids are some of the most conspicuous inhabitants of modern vent and seep ecosystems, and ancient vent and seep tubular fossils are usually considered to have been made by annelids. However, the taxonomic affinities of many tube fossils from vents and seeps are contentious, or have remained largely undetermined due to difficulties in identification. In this study, we make a detailed chemical (Fourier-transform infrared spectroscopy and pyrolysis gas-chromatography mass-spectrometry) and morphological assessment of modern annelid tubes from six families, and fossil tubes (seven tube types from the Cenozoic, 12 Mesozoic and four Palaeozoic) from hydrothermal vent and cold seep environments. Characters identified from these investigations were used to explore for the first time the systematics of ancient vent and seep tubes within a cladistic framework. Results reveal details of the compositions and ultrastructures of modern tubes, and also suggest that two types of tubes from ancient vent localities were made by the annelid family Siboglinidae, which often dominates modern vents and seeps. Our results also highlight that several vent and seep tube fossils formerly thought to have been made by annelids cannot be assigned an annelid affiliation with any certainty. The findings overall improve the level of quality control with regard to interpretations of fossil tubes, and, most importantly, suggest that siboglinids likely occupied Mesozoic vents and seeps, greatly increasing the minimum age of the clade relative to earlier molecular estimates.
“…These are superficially similar to those produced by serpulid (polychaete annelid) worms in modern marine environments. However, true serpulid structures are restricted to younger deposits (Vinn and Mutvei 2009;Ippolitov et al 2014). Crinoid ossicles vary from being relatively densely encrusted-close to 10% of surface area covered; Fig.…”
The cladid crinoid Diphuicrinus ohioensis Burke, 1976, was originally described from shallow marine facies of the Middle Pennsylvanian Putnam Hill Limestone of southeastern Ohio. One of the type localities for this taxon is an abandoned quarry in Vinton County, where a small number of articulated cups used in erection of this species was collected. Prior to formal description of this species, multiple isolated calyx ossicles were collected from this locality, but were not analyzed in detail or included in the description of D. ohioensis. The previously unidentified material, described herein, contributes to a more complete record of this taxon. Further, heavily sculptured (nodose) basal and radial plates are nearly ubiquitously encrusted by calcareous tubes, a paleoecological detail not otherwise noted in the description of D. ohioensis or the lithofacies from which material was collected. Encrusters, which consist of at least 2 varieties, are present primarily in depressed areas in between raised nodes. This may reflect post-mortem removal via abrading currents but may alternatively represent preferential encrustation of portions of hard bioclasts characterized by larger, smoother, protected surfaces. This study reinforces the value of isolated crinoid ossicles in paleoecology, paleobiology, and paleoenvironmental analysis.
Serpulids are marine filter-feeding annelids that live in calcareous tubes. Their distribution, colonization, and proliferation are dependent on physical environmental variables, including energy conditions. This article documents the occurrences of serpulid colonies over opportunistic colonizing trace fossil of Ophiomorpha-rich sedimentary unit in the Lower Maastrichtian Kallankurichchi Formation of the Ariyalur Group, Cauvery Basin, South India and links them with ecosystem dynamics, as a function of changes in eustatic and other relative sea-level changes and attendant variations in environmental parameters. Present observations indicate episodic changes in faunal composition, diversity, and population, across the boundary between Kattupiringiyam Inoceramus limestone Member and Tancem biostromal Member of the Kallankurichchi Formation. The boundary marked a significant change from lowmoderate energy, to high-energy waters, thus replacing a filter-feeding community by an opportunistic community. The opportunistic colonizers/trace makers of Ophiomorpha irregulaire occupied the ecospaces vacated by the sea-level changes.Systematic studies of faunal association across the boundary indicate a sudden appearance of significant populations of Serpula colonies above the surface (i.e., after the changes in ecosystem conditions) and enhancement of intensity of sponge boring in benthic organisms. This means that the changes brought about by the newer environmental conditions were supportive for opportunistic colonizers followed by parasitic and commensalic organisms. Significant reduction of Gryphaea population that was increasingly replaced by Alectryonia, Exogyra, and Terebratula is also documented. These changes, collectively, indicate prevalent environmental stress due to relative sea-level variations and attendant ecological conditions, to which, the opportunistic colonizers and parasitic organisms responded positively, while the native organisms dwindled in population and were forced to parasitic invasions.
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