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Journal Article
Published: 01 August 2014
European Journal of Mineralogy (2014) 26 (4): 517–522.
... attachment organ (byssus) of the marine bivalve Anomia simplex . We compare two approaches to studying the biomolecule-induced lattice deformation: X-ray diffraction of annealed samples and in situ heating X-ray diffraction. In the latter case, the lattice deformation is obtained by extrapolation...
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First thumbnail for: Lattice macro and microstrain fluctuations in the ...
Second thumbnail for: Lattice macro and microstrain fluctuations in the ...
Third thumbnail for: Lattice macro and microstrain fluctuations in the ...
Journal Article
Published: 01 September 1969
Journal of Paleontology (1969) 43 (5): 1125–1129.
... of trigonian ontogeny? There is no firm evidence for the existence of a byssus in Mesozoic adult trigonians. Gould favors the hypothesis that the trigonian byssus is functional in juveniles for two reasons: Most, and perhaps all, bivalves are byssally attached in the post-larva and several prolong this habit...
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 Figure1—Drawing of a Pinna nobilis individual as is usually found with the tapered anterior third of the shell buried in the sediment, attached to the substratum by byssus threads. Each rectangle delimits the portions of the shell shown in subsequent figures
Published: 01 May 2008
Figure 1 —Drawing of a Pinna nobilis individual as is usually found with the tapered anterior third of the shell buried in the sediment, attached to the substratum by byssus threads. Each rectangle delimits the portions of the shell shown in subsequent figures
Journal Article
Published: 01 January 2008
Journal of Paleontology (2008) 82 (1): 102–117.
... retractor muscles generally supported by myophores. Lamychaena evolved from Rocellaria during the Oligocene, extending its ctenidia far posterior into the siphonal part of the boring, and, in some species, uniting its anterior pedal retractor and protractor muscles as they approach the byssus apparatus...
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First thumbnail for: THE IDENTITY OF GASTROCHAENA CUNEIFORMIS SPENGLER,...
Second thumbnail for: THE IDENTITY OF GASTROCHAENA CUNEIFORMIS SPENGLER,...
Third thumbnail for: THE IDENTITY OF GASTROCHAENA CUNEIFORMIS SPENGLER,...
Series: Geological Society, London, Special Publications
Published: 01 January 2000
DOI: 10.1144/GSL.SP.2000.177.01.32
EISBN: 9781862394254
... Abstract The evolution of the heteromyarian form and neotenous retention of the byssus into the adult stage were central to the colonization of hard substrata and the subsequent evolutionary success of epibyssate mytilids. In addition, these mussels are supreme filter feeders and exhibit many...
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Experimental strategy and example powder diffractograms. (A) Byssi were powdered and used in three different experiments (marked A–C). (B) Comparison of excerpts of powder diffractograms from experiments A and B from non-annealed samples (RT) and samples annealed at 623 K (350°C). The star indicates a reflection from quartz that was connected to the byssus. (C) Excerpts of diffraction patterns from experiment C shown from 300–895 K in steps of 35 K. (Online version in color)
Published: 01 August 2014
indicates a reflection from quartz that was connected to the byssus. (C) Excerpts of diffraction patterns from experiment C shown from 300–895 K in steps of 35 K. (Online version in color)
Image
Figure 1. Ontogenetic changes in the life position of Mercenaria mercenaria that relate to the vulnerability of juveniles to predation. The postlarval form is attached to sand grains by a byssus (A). Relatively elongate siphons of an individual slightly more than 2 cm long (B) position its shell approximately as deep as that of an adult (D). Elongate siphons of a juvenile slightly more than 4 cm long (C) allow it to burrow much deeper than an adult. This kind of ontogenetic shift is typical of the bivalve family Veneridae (From Stanley 1972)
Published: 01 February 2008
Figure 1. Ontogenetic changes in the life position of Mercenaria mercenaria that relate to the vulnerability of juveniles to predation. The postlarval form is attached to sand grains by a byssus (A). Relatively elongate siphons of an individual slightly more than 2 cm long (B) position its shell
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Figure2—Sketch diagram showing possible life positions of N. trigonimimus n. gen. and sp. attached to rocks, shell fragments, or hard sediment. The case for mimicry must await evidence for attachment to the area or escutcheon of semi-infaunal Steinmanella transitoria (Steinmann, 1881). The convergent surface ornamentation of both species form mirror-image replicas of one another. 1, Possible attachment to S. transitoria, not observed; 2, attachment to a buried rock or pebble; 3, attachment to a surface elevated above the substrate; 4, anterior face showing lunule and curved commissure with narrow slit for byssus
Published: 01 November 2004
commissure with narrow slit for byssus
Image
 Figure5—Living specimens of two species of Lamychaena Freneix inFreneix and Roman, 1979, one from the Indian Ocean (1, 3), the other from the Western Atlantic (2). 1,3, Lamychaena weinkauffi (Sturany, 1899), Balaclava Bay, Mauritius; 1, posterior of siphons, incurrent on right, UNC 15855; 3, left side of animal with partially extended siphons, showing byssus (on red background) and extended, digitate toe on foot, UNC 15858. 2,Lamychaena hians (Gmelin, 1791), Butler Bay, St. Croix, U.S. Virgin Islands, West Indies, UNC 15248, posterior of siphons, incurrent on left. Bar scales = 1 mm in 1 and 2; 5 mm in 3
Published: 01 January 2008
, UNC 15855; 3 , left side of animal with partially extended siphons, showing byssus (on red background) and extended, digitate toe on foot, UNC 15858. 2, Lamychaena hians ( Gmelin, 1791 ), Butler Bay, St. Croix, U.S. Virgin Islands, West Indies, UNC 15248, posterior of siphons, incurrent on left
Journal Article
Journal: PALAIOS
Published: 01 December 2007
PALAIOS (2007) 22 (6): 612–622.
... life habits at sizes greater than 2 mm. A classic case is Mercenaria mercenaria (Veneridae), which is a shallow, unattached burrower as an adult. Juveniles alternate between byssal attachment and active crawling, with the byssus lost at an average shell length of 7 mm ( Carriker, 1961 , p. 184...
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First thumbnail for: POTENTIAL PALEOECOLOGIC BIASES FROM SIZE-FILTERING...
Second thumbnail for: POTENTIAL PALEOECOLOGIC BIASES FROM SIZE-FILTERING...
Third thumbnail for: POTENTIAL PALEOECOLOGIC BIASES FROM SIZE-FILTERING...
Journal Article
Published: 01 July 1996
Canadian Journal of Earth Sciences (1996) 33 (7): 993–1006.
... morphologie fonctionnelle de P. semiplicata suggère pour le stade ontogénique précoce un mode de vie fixée par un byssus, passant ensuite à la position couchée avec adaptation aux sédiments mous. On a observé souvent que l'espèce laissait un pavé de coquilles dans les pélites de couleur sombre avec absence...
Journal Article
Journal: Paleobiology
Published: 01 August 2021
Paleobiology (2021) 47 (3): 503–516.
... epifaunal mode of life. They are both frequently attached to hard substrates (e.g., stones, corals, mollusk shells) by a proteinaceus byssus emerging from the anterior-ventral margin. Most Carditinae species have a byssal gape (with a variable degree of development) for the passage of this byssus...
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First thumbnail for: The incubatory chamber of marsupial carditids (Biv...
Second thumbnail for: The incubatory chamber of marsupial carditids (Biv...
Third thumbnail for: The incubatory chamber of marsupial carditids (Biv...
Journal Article
Published: 01 November 2006
Journal of Micropalaeontology (2006) 25 (2): 187–188.
.... The surface of the sediment was covered by the byssus of the mussel Musculista senhousia ( Benson, 1842 ). Sanyuania cuneata is probably endemic to the East China Sea and the southwestern part of the Sea of Japan and is a potentially useful palaeoenvironmental indicator of brackish (steno-haline...
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First thumbnail for: Sanyuania cuneata Zhao & Whatley, 1992 (Ostrac...
Second thumbnail for: Sanyuania cuneata Zhao & Whatley, 1992 (Ostrac...
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Examples of colonization on hard substrata. A) Large oncoid (15 cm in diameter) intensely bored on all surfaces by Lithophaga lithophaga (which produced the bioerosion structure Gastrochaenolites torpedo), with borings of other endolithic bivalves (producing G. lapidicus). The surface was secondarily bored and grazed by sponges (producing Entobia isp.), even in the interior of the G. torpedo, and encrusted by ostreids, serpulids, and calcareous algae (Lithophyllum isp.); base of Pliocene, Crevillente B section. B) Polished section of a planar and LLH (lateral linked hemispheroidal) stromatolite topped by an initial colonization of G. lapidicus? and a second generation of Entobia isp.; base of Pliocene, Crevillente B section. C) Ostreid valve intensely bored by Entobia isp. and showing attachment of bivalve byssus (Centrichnus isp.); base of Pliocene, Elche section. D) Hardground with Trypanites isp. and secondary G. torpedo, truncated and crosscut by successive coastal erosion; Messinian–Pliocene boundary, Colmenar section. E) Free-lying aggregate of oyster balls (ostreolith, sensu Taylor and Wilson, 2003) intensely colonized by bryozoan, serpulid, and Lithophyllum isp.; base of Pliocene, CAM section. F) Coastal rolling stone with undifferentiated Gastrochaenolites, echinoid-grazing traces (probable Gnathichnus isp.), Maeandropolydora isp., and Caulostrepsis isp. (endolithic activity of polychaete annelids); base of Pliocene, CAM section.
Published: 01 December 2011
) stromatolite topped by an initial colonization of G. lapidicus? and a second generation of Entobia isp.; base of Pliocene, Crevillente B section. C) Ostreid valve intensely bored by Entobia isp. and showing attachment of bivalve byssus (Centrichnus isp.); base of Pliocene, Elche section. D) Hardground
Journal Article
Published: 01 May 2008
Journal of Paleontology (2008) 82 (3): 555–564.
.... orientalis Bittner, 1891 ), Bittner (1891) had only right valves at hand, only one of which showed hinge details. In this specimen ( Bittner, 1891 , pl. 2, fig. 10a), the anterior shell margin is inwardly folded below the beaks and thereby creates a gape for the passage of the byssus. The dorsal shell...
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First thumbnail for: Taxonomy and Phylogeny of the Triassic Bivalve Fam...
Second thumbnail for: Taxonomy and Phylogeny of the Triassic Bivalve Fam...
Third thumbnail for: Taxonomy and Phylogeny of the Triassic Bivalve Fam...
Journal Article
Published: 01 March 1998
Russ. Geol. Geophys. (1998) 39 (3): 415–418.
... and inocerams. This fact is evidence of the periodical oxygen saturation of the bottom waters even at the lowest sites of the bottom. Otherwise, the bivalve larvae could not have successfully developed in the water with a great deficit of oxygen. Buchia and inocerams belong to the seston-eating byssus epifaunal...
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First thumbnail for: FIRST OCCURRENCE OF TRACE FOSSILS IN HIGHLY CARBON...
Journal Article
Published: 01 November 2010
Journal of Paleontology (2010) 84 (6): 1152–1176.
... on the surfaces of the LVs supports this interpretation (e.g., Fig. 10.3 ), although it is possible that the association with epifauna might have occurred postmortem. The presence of a distinct posterior pedo-byssal retractor muscle scar suggests the presence of the byssus. Modern pterioideans that lack...
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First thumbnail for: Cassiavellia galtarae , New Species, New Genus: A ...
Second thumbnail for: Cassiavellia galtarae , New Species, New Genus: A ...
Third thumbnail for: Cassiavellia galtarae , New Species, New Genus: A ...
Journal Article
Published: 01 May 2018
Journal of Paleontology (2018) 92 (3): 388–397.
... on the variation of its morphology. The chosen landmarks, additionally, captured the position of auricles and byssus in relation to the shell body, adding information beyond the outline of the shell disk. ?1884 Actinopteria theta Hall , p. 125, pl. 84, figs. 18, 19. Skaneateles Formation: Pompey Road Cut...
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First thumbnail for: Ecophenotypic variability during times of evolutio...
Second thumbnail for: Ecophenotypic variability during times of evolutio...
Third thumbnail for: Ecophenotypic variability during times of evolutio...
Journal Article
Published: 01 May 2010
Journal of Paleontology (2010) 84 (3): 549–553.
... collagen in mussel byssus: a natural block copolymer : Science , 277 . 1830 – 1832 . Durham , J. W. , 1978 , A Lower Cambrian eocrinoid : Journal of Paleontology , 52 . 195 – 199 . Jaekel , O. , 1918 , Phylogenie und system der Pelmatozoen : Paläontologische Zeitschrift , 3...
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First thumbnail for: A NEW TURBAN-SHAPED GOGIID EOCRINOID FROM THE KAIL...
Second thumbnail for: A NEW TURBAN-SHAPED GOGIID EOCRINOID FROM THE KAIL...
Third thumbnail for: A NEW TURBAN-SHAPED GOGIID EOCRINOID FROM THE KAIL...
Journal Article
Published: 01 May 2008
Journal of Paleontology (2008) 82 (3): 621–627.
...Figure 1 —Drawing of a Pinna nobilis individual as is usually found with the tapered anterior third of the shell buried in the sediment, attached to the substratum by byssus threads. Each rectangle delimits the portions of the shell shown in subsequent figures ...
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First thumbnail for: The Duplivincular Ligament of Recent Pinna Nobilis...
Second thumbnail for: The Duplivincular Ligament of Recent Pinna Nobilis...
Third thumbnail for: The Duplivincular Ligament of Recent Pinna Nobilis...