Survival of crinoid stems following decapitation: evidence from the Ordovician and palaeobiological implications

It was recently discovered that the stems of extant crinoids may survive after detachment of the crown, presumably feeding by the absorption of nutrients through the ectoderm. Previously, only one analogous, albeit morphologically dissimilar, pattern of crownless survival has been recognized from the fossil record. Certain Upper Ordovician (Cincinnatian) crinoid pluricolumnals from Kentucky, Ohio and Indiana, derived from the disparids Cincinnaticrinus spp., have rounded terminations reminiscent of some modern bourgueticrinid overgrowths. Such specimens have hitherto been interpreted as distal terminations of mature individuals that have become detached from their attachment structures and taken to an eleutherozoic existence. However, it is considered more probable that they represent overgrowths of the column following predatory decapitation. If this new interpretation is correct, then post-decapitation survival of crinoid stems is now recognized for most of the history of the crinoids, 'lethal' predation on crinoid crowns occurred at least as early as the Late Ordovician and ancient crinoid populations can no longer be determined merely by counting crowns.     

Cyrtocrinids (Cyrtocrinida,Crinoidea) and other associated crinoids from the Jurassic (Kimmeridgian–Tithonian)–Cretaceous (Berriasian–Barremian) of the Carpathian Foredeep basement (western Ukraine)

Upper Jurassic (Kimmeridgian–Tithonian) and Cretaceous (Berriasian–Barremian) strata of the Ukrainian part of the Carpathian Foredeep basement are rich, at least locally, in crinoid remains. Crinoids belonging to cyrtocrinids (Cyrtocrinida) are represented by whole cups, isolated remains of disarticulated cups, brachial plates and columnals. They are assigned to the following taxa: Cyrtocrinida indet., Eugeniacrinites cf. cariophilites (von Schlotheim), Lonchocrinus sp., Phyllocrinus stellaris Zaręczny, Ascidicrinus pentagonus (Jaekel), Gammarocrinites sp., Psalidocrinus armatus (Zittel), Psalidocrinus sp., and Hemibrachiocrinidae gen. indet. Cyrtocrinids are associated with other stalked (isocrinids, Isocrinida and millericrinids, Millericrinida) and stemless (saccocomids, Roveacrinida) crinoids. Columnals, pluricolumnals, brachial plates, and cirrals of isocrinids are assigned to Balanocrinus sp., Isocrinina fam. et subfam. indet., and columnals of millericrinids to Millericrinida indet. Free-living roveacrinids are assigned to Saccocoma sp. and Crassicoma sp. Knowledge on Jurassic and Cretaceous crinoids formerly described from Ukraine is discussed. Although majority of crinoids described herein seems to be allochthonous, autochthonous forms were also found with certainty in some intervals. These include some cyrtocrinids, which dominate in shallow-water environments of the Ukrainian Carpathian Foredeep basement. Isocrinids are also common in this shallow marine environment, whereas sessile saccocomids are assigned to low-energy, mud-supported bottom, open marine, outer-platform/upper slope, and relatively deep environments.     

Visceral regeneration in the crinoid Antedon mediterranea: basic mechanisms, tissues and cells involved in gut regrowth

Crinoids are able to regenerate completely many body parts, namely arms, pinnules, cirri, and also viscera, including the whole gut, lost after self-induced or traumatic mutilations. In contrast to the regenerative processes related to external appendages, those related to internal organs have been poorly investigated. In order to provide a comprehensive view of these processes, and of their main events, timing and mechanisms, the present work is exploring visceral regeneration in the feather star Antedon meditteranea. The histological and cellular aspects of visceral regeneration were monitored at predetermined times (from 24 hours to 3 weeks post evisceration) using microscopy and immunocytochemistry. The overall regeneration process can be divided into three main phases, leading in 3 weeks to the reconstruction of a complete functional gut. After a brief wound healing phase, new tissues and organs develop as a result of extensive cell migration and transdifferentiation. The cells involved in these processes are mainly coelothelial cells, which after trans-differentiating into progenitor cells form clusters of enterocytic precursors. The advanced phase is then characterized by the growth and differentiation of the gut rudiment. In general, our results confirm the striking potential for repair (wound healing) and regeneration displayed by crinoids at the organ, tissue and cellular levels.     

Pseudoplanktonic lifestyle of the Triassic crinoid Traumatocrinus from Southwest China

Colonies of Traumatocrinus (Echinodermata, Crinoidea) attached to driftwood from the lower Upper Triassic (Carnian) Xiaowa Formation of the Guanling area (Guizhou, Southwest China) document a pseudoplanktonic lifestyle for this specialized offshoot of the otherwise benthic Middle Triassic Encrinidae. After the end-Carnian decline of Traumatocrinus, its ecological niche was subsumed in Norian by genera derived from another benthic family (Holocrinidae) with convergent morphological modifications. After the Toarcian (Lower Jurassic), this niche disappeared, possibly due to the emergence of wood-boring bivalves.     

Cyrtocrinids (Crinoidea) and associated stalked crinoids from the Lower/Middle Oxfordian (Upper Jurassic) shelfal deposits of southern Poland

Five cyrtocrinid crinoid taxa previously unknown from the epicratonic deposits of Poland, as well as associated millericrinids and isocrinids, are described. The studied materials were derived mainly from the Lower and Middle Oxfordian, but crinoids are also from uppermost Callovian and/or lowermost Oxfordian sediments of the Polish Jura Chain (southern Poland). The crinoids, preserved as more or less complete (e.g., basal circlets) cups, include Lonchocrinus dumortieri, Phyllocrinus belbekensis, Remisovicrinus polonicus, Remisovicrinus aff. polonicus, Tetracrinus moniliformis and Sclerocrinus sp. The occurrence of Remisovicrinus polonicus in the late Middle Oxfordian of the southern Poland is confirmed. Moreover, the present study extends the geographic range of all cyrtocrinid species studied and discusses their unusual environmental adaptations.     

New multiarmed crinoids of the family Catillocrinidae from the Lower Permian of the Fore-Urals

New Catillocrinidae Allocatillocrinus rarus sp. nov., with a previously unknown tegmenal structure, Paracatillocrinus shamovi sp. nov., and P. shakhtauensis sp. nov., with an unusual relative position of the crown and stem are described from the Artinskian Stage (Lower Permian) of the western slope of the Middle and Southern Ural Mountains (Boets, Krasnoufimsk, and Shakh-Tau localities). The genus Allocatillocrinus has not previously been recorded from the Permian, while Paracatillocrinus has only previously been reported from the Upper Permian of Timor Island.     

Late Jurassic (Kimmeridgian) sea lilies (Crinoidea) from central Poland (Łódź Depression)

Upper Jurassic (Kimmeridgian) limestones of central Poland (southern border of the ?ód? Depression) are in places extremely rich in crinoid remains. These latter are represented by very well preserved columnals/pluri-columnals, isolated brachials and cirrals/pluri-cirrals, assignable to the following species: Isocrinus amblyscalaris (Thurmann, in Thurmann and Éttalon), Isocrinus cf. pendulus (von Meyer), Balanocrinus brachiospina Hess, Balanocrinus pentagonalis (Goldfuss), Balanocrinus subteres (Münster, in Goldfuss), Balanocrinus sp., and Millericrinida indet. The commonest species, Balanocrinus brachiospina, is recorded for the first time from Poland. Critical revision of Polish occurrence of balanocrinids is provided. It is suggested that some of the previous balanocrinid finds from Poland assigned to Balanocrinus subteres should be now addressed as B. brachiospina. Furthermore, it is probable that the Callovian B. hessi Salamon and Zatoń should be synonymized with B. pentagonalis. Crinoid material at hand is also associated with asteroid and echinoid remains. Among this material, a complete test of Pleurodiadema nudum Cotteau is illustrated for the first time from Poland. Taphonomic observations of echinoderms from the Kimmeridgian limestones of the ?ód? Depression suggest that they did not undergo a long post-mortem transport. The high degree of disarticulation, however, supports their prolonged post-mortem seafloor exposure.     

Unusual tabulate‐crinoid biocoenosis from the Lower Devonian of Morocco

The Early Devonian (Pragian: sulcatus to pireneae conodont zones) crinoid–coral biocoenosis from Hamar Laghdad, Morocco contains fragments of crinoid stalks of various taxa encrusted by spherical and ellipsoidal coralla of the tabulate coral Hamarilopora minima. These corals were encrusting host crinoids syn vivo, and this is evidenced by pluricolumnals exceeding 30 elements overgrown from all sides. Most known to date crinoid–epibiont associations display various types of reaction to the epibiont, such as swellings and deformations. In the case discussed here, no clear interaction is visible; therefore, this association can be classified as paroecia. It can be inferred, however, that due to a change in mechanical properties of the crinoid stalk (losing flexibility), the epizoan influence on the host was negative, while the coral was profiting from the elevated position over the seafloor and nutrient‐bearing water currents. It can be supposed that this interaction was close to parasitism. No strict species‐specific relationship between the epizoan and the host was observed.     

Infestation of Middle Devonian (Givetian) camerate crinoids by platyceratid gastropods and its implications for the nature of their biotic interaction

One of the classic examples of biotic interactions preserved in the fossil record is that between crinoids and infesting platyceratid gastropods. This relationship, spanning an interval from the Middle Ordovician to the end of the Permian, is recognized by the firm attachment and positioning of platyceratids over the anal vent of their hosts. Several hypotheses have been proposed to explain this interaction; the most widely accepted is that the gastropods were coprophagous commensals, feeding on crinoid excrement without any significant detriment to their hosts. The purpose of this investigation was to test this hypothesis. Two species of Middle Devonian camerate (Monobathrida, Compsocrinina) crinoids, Gennaeocrinus variabilis Kesling & Smith 1962 and Corocrinus calypso (Hall 1862), were used in this investigation. The data consisted of 426 individuals of G. variabilis collected near Rockport, Michigan, 30 of which were infested, and 188 individuals of C. calypso collected near Arkona, Ontario, Canada, of which 25 were infested. Length and volume were measured for each crinoid to determine whether a significant difference existed in the size of infested versus uninfested individuals. The results indicated that for both species of crinoids individuals infested by snails were significantly smaller than uninfested individuals (p < 0.05). We explored a variety of scenarios to explain this pattern and conclude that they falsify the null hypothesis that the crinoid-gastropod relationship was strictly commensal. The smaller size of the infested crinoids is interpreted as a consequence of nutrient-stealing by the parasitic gastropods, a strategy that finds analogs in modern seas. Moreover, the absence of platyceratids on the largest crinoids suggests that large size may have inferred immunity from lasting infestation.     

NEW CLADID AND FLEXIBLE CRINOIDS FROM THE MISSISSIPPIAN (TOURNAISIAN, IVORIAN) OF ENGLAND AND WALES

Abstract:  The modern study of fossil crinoids began with J. S. Miller who, in 1821, described specimens from southern England, nearby Wales and other regions, and named several common Early Carboniferous genera. Later, in 1950–60, James Wright monographed all known Early Carboniferous crinoids from the British Isles. In spite of such previous scrutiny, we recognize here two new genera among species already described: Glamorganocrinus gen. nov. (type species: Ophiurocrinus gowerensis Wright, 1960) from South Wales and Mendipocrinus gen. nov. (type species: Poteriocrinus latifrons Austin and Austin, 1847) from southern England. These new genera increase the number of advanced cladid genera in the Ivorian Substage of the Tournaisian in western Europe to 18, and the total number of crinoid genera to 36. A review of species assigned to Mespilocrinus has led to the recognition of M. granulifer De Koninck and LeHon, 1854 as a nomen dubium. A new species of Mespilocrinus , M. wrighti sp. nov., is described from the Ivorian of South Wales; this is the most highly derived species of the genus, as based on a phylogenetic analysis including ten species and 13 characters, with Pycnosaccus as the outgroup. A single, well-ordered tree resulted from this analysis. Interpretation of this tree suggests that the centre of evolution for Mespilocrinus was North America, where three species appeared during the Kinderhookian (early Tournaisian), rapidly achieving morphological disparity within the genus. This radiation event was part of the overall explosive radiation of crinoids following the Late Devonian mass extinction event when crinoid diversity was at a global minimum during the Frasnian. Recovery began during the Famennian, followed by an explosive radiation in the Tournaisian.