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Nassariidae

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Journal Article
Published: 01 January 2011
Journal of Paleontology (2011) 85 (1): 178.
... sense (restricted to the marine Indo-West Pacific region) a global phylogenetic analysis of Nassariidae is needed before its proper allocation can be determined, as already noted by Vermeij and Wesselingh (2002) . We here rename the Peruvian fossil as Nassarius (s.l.) wesselinghi in honor of Frank...
Journal Article
Published: 01 September 2000
Journal of Paleontology (2000) 74 (5): 839–852.
...D. M. HAASL Abstract Phylogenetic relationships within the neogastropod family Nassariidae are poorly understood as are relationships between the Nassariidae and other fossil and extant buccinid taxa. The poor resolution of nassariid and buccinoidean relationships is due to: 1) the complex...
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First thumbnail for: PHYLOGENETIC RELATIONSHIPS AMONG NASSARIID GASTROP...
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Journal Article
Published: 01 February 2023
Journal of Paleontology (2023) 97 (S91): 1–42.
...Warren D. Allmon; Dana S. Friend Abstract Numerous species of “oliviform” gastropods have been recognized in the Paleogene of the U.S. Gulf Coastal Plain, many of which have previously been allied to the “ Bullia group” in the family Nassariidae, and placed in a variety of poorly defined genera. We...
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First thumbnail for: Review and revision of the Olivoidea (Neogastropod...
Second thumbnail for: Review and revision of the Olivoidea (Neogastropod...
Third thumbnail for: Review and revision of the Olivoidea (Neogastropod...
Journal Article
Published: 01 March 2002
Journal of Paleontology (2002) 76 (2): 265–270.
...), and ? Nassarius reductus (Nassariidae) is recognized as a new species. These gastropods are among the very few marine invaders in the otherwise freshwater Pebas fauna. The small number of marine to freshwater transitions among South American molluscs contrasts with the situation among South American fishes...
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First thumbnail for: NEOGASTROPOD MOLLUSCS FROM THE MIOCENE OF WESTERN ...
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Published: 01 September 2000
Table 1 —Taxa names and classification used in the phylogenetic analysis. Taxonomic classification is largely after Cernorhorsky (1984). Cylleninae, the third nassariine subfamily, was not included in the analyses and so is omitted from this table. In all analyses, the Nassariidae comprised
Journal Article
Journal: Paleobiology
Published: 01 May 2021
Paleobiology (2021) 47 (2): 337–362.
... ), and Friend ( 2020 ). A single representative in Kantor et al. ( 2017 ) places Volutidae outside Nassariidae. Either position does not impact our interpretation. CL, crossed-lamellar. Table 1. Synopsis of the microstructures employed in the construction of callus, extreme parietal callus (EPC...
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First thumbnail for: Convergence, parallelism, and function of extreme ...
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Journal Article
Published: 01 November 2004
Journal of Paleontology (2004) 78 (6): 1123–1127.
.... These same sculptural features are consistent with placement of Mexfusus in Buccinoidea in the sense of F. Riedel (2000) and Harasewych and Kantor (2002) , a clade that contains such families as Buccinidae, Fasciolariidae, Melongenidae, and Nassariidae. Axial sculpture that diminishes on or disappears...
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First thumbnail for: MEXFUSUS ROTUNDICOSTATUS , A NEW GENUS AND SPECIES...
Second thumbnail for: MEXFUSUS ROTUNDICOSTATUS , A NEW GENUS AND SPECIES...
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Phylogeny of Caenogastropoda showing occurrence of extreme parietal callusing. Families where the extreme parietal callus (EPC) is known to occur in at least one species are in bold font. The microstructures employed in the construction of the callus are indicated by colored cross bars (For reference to colors indicated in the key, the reader is directed to the online version.) Filled circles indicate the EPC is present in the species, open circles indicate no EPC, and a partially filled circle was used to indicate enlarged (but not extreme) callus. †Indicates extinct species. The EPC is uncommon in all families examined (see Supplementary Table 1); however, only calloused and control (examined non-EPC) species are shown. Therefore, this figure should not be interpreted as indicating the EPC is primitive for any clade. Phylogeny modified from the strict consensus morphological tree of Ponder et al. (2008), using the phylogenies of Simone (2005), Kantor et al. (2017), Strong et al. (2019), and Friend (2020). A single representative in Kantor et al. (2017) places Volutidae outside Nassariidae. Either position does not impact our interpretation. CL, crossed-lamellar.
Published: 01 May 2021
of Ponder et al. ( 2008 ), using the phylogenies of Simone ( 2005 ), Kantor et al. ( 2017 ), Strong et al. ( 2019 ), and Friend ( 2020 ). A single representative in Kantor et al. ( 2017 ) places Volutidae outside Nassariidae. Either position does not impact our interpretation. CL, crossed-lamellar.
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Phylogenetic distribution of septa in caenogastropods. Supertree phylogeny of caeonogastropods based on the strict-consensus tree obtained from Bayesian analysis of the combined molecular and morphological data set performed by Ponder et al. (2008), with modification to cerithioidean relationships based on Strong et al. (2011), and the positions of Pomatiidae, Caecidae, and Buccinidae inferred based on the superfamilial relationships in Bouchet et al. (2005). Data for Siliquariidae (Bieler 2004), Planorbidae (Brown et al. 1984), Subulinidae (Rumininae) (Hochpöchler and Kothbauer 1975), Clausiliidae (Pall-Gergely and Nemeth 2008), Campanilidae (Houbrick 1981), Thiaridae (Fretter and Graham 1962), Caecidae (Fretter and Graham 1962), Ranellidae (Bandel 1979), Nassariidae (Fortey 2009), Volutidae (Ford 2006), and Muricidae (Bandel 1979) were obtained from the literature. Septa were detected in all other taxa using CT scans, SEM, or visual observation. Ancestral states inferred through parsimony. Green colors indicate that septa are present. Light green indicates taxa in which the septum is thin and apically convex. Dark green indicates taxa in which septa are thick. Yellow-green indicates taxa that possess septa of ambiguous morphology. Red indicates taxa that were examined and found not to possess septa. Brown indicates unknown ancestral states. Consult Supplementary Fig. S6 for enlarged images.
Published: 30 May 2018
1975 ), Clausiliidae (Pall-Gergely and Nemeth 2008 ), Campanilidae (Houbrick 1981 ), Thiaridae (Fretter and Graham 1962 ), Caecidae (Fretter and Graham 1962 ), Ranellidae (Bandel 1979 ), Nassariidae (Fortey 2009 ), Volutidae (Ford 2006 ), and Muricidae (Bandel 1979 ) were obtained from
Journal Article
Published: 01 September 2007
South African Journal of Geology (2007) 110 (2-3): 327–338.
... of the gastropod Nassarius vinctu s (<15 mm), retrieved by multicorer, were observed living on the sediment surface, with shells often coated by algae. These members of the family Nassariidae are active scavengers on muddy substrates and may live in large colonies ( Kilburn and Rippey, 1982 ). Nassariidae...
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First thumbnail for: Geochronology of Holocene sediments on the western...
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Journal Article
Journal: Paleobiology
Published: 30 May 2018
Paleobiology (2018) 44 (3): 444–459.
... 1975 ), Clausiliidae (Pall-Gergely and Nemeth 2008 ), Campanilidae (Houbrick 1981 ), Thiaridae (Fretter and Graham 1962 ), Caecidae (Fretter and Graham 1962 ), Ranellidae (Bandel 1979 ), Nassariidae (Fortey 2009 ), Volutidae (Ford 2006 ), and Muricidae (Bandel 1979 ) were obtained from...
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First thumbnail for: When domes are spandrels: on septation in turritel...
Second thumbnail for: When domes are spandrels: on septation in turritel...
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Journal Article
Published: 01 October 2016
Italian Journal of Geosciences (2016) 135 (3): 540–547.
... . Manganelli G. Spadini V. Martini I. ( 2010 ) - Rediscovery of an enigmatic Euro-Mediterranean Pliocene nassariid species: Nassarius crassiusculus Bellardi, 1882 (Gastropoda: Nassariidae) . Boll. Soc. Paleont. It. , 49 , 195 – 202 . Marinelli G . ( 1975 ) - Magma evolution in Italy...
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First thumbnail for: Calcareous plankton bio-chronostratigraphy and sed...
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Journal Article
Published: 01 October 2015
Journal of Paleontology (2015) 89 (3): 487–493.
.... , da Silva C.M. , and Gili C ., 2009 , The early Pliocene Gastropoda (Mollusca) of Estepona, southern Spain, part 8, Nassariidae : Palaeontos , v. 17 , p. 35 – 102...
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First thumbnail for: First record of buccinid genus Chauvetia (Mollusca...
Second thumbnail for: First record of buccinid genus Chauvetia (Mollusca...
Journal Article
Journal: PALAIOS
Published: 01 January 2015
PALAIOS (2015) 30 (1): 116–127.
... al. 1998 ; Bouchet et al. 2011 ). Nassariidae are also common, represented by four species (123 specimens; Fig. 3N–P ), two of which are among the ten most abundant taxa. Members of the family largely feed on carrion, although they may shift facultatively to plant matter ( Brown 1969 ). Suspension...
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First thumbnail for: DIVERSITY AND PALEOECOLOGY OF MIOCENE CORAL-ASSOCI...
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Journal Article
Journal: PALAIOS
Published: 01 November 2009
PALAIOS (2009) 24 (11): 772–779.
... of shell-boring predation by a representative of the Nassariidae (Gastropoda) : Journal of Molluscan Studies , 63 . 480 – 482 . Nebelsick , J. H. , and Kowalewski , M. , 1999 , Drilling predation on recent clypeasteroid echinoids from the Red Sea : PALAIOS , 14 . 127 – 144...
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First thumbnail for: TAPHONOMIC BIAS ON DRILL-HOLE PREDATION INTENSITIE...
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Journal Article
Published: 01 January 2022
Journal of Paleontology (2022) 96 (1): 143–151.
... of univalve shells, for the reception of certain species of Bruguière's genus Cassis : The Annals and Magazine of Natural History (n.s.) , v. 1 , p. 214 – 217 . Van Dingenen , F. , Ceulemans , L. , Landau , B.M. , and Silva , C.M., da , 2015 , The family Nassariidae (Gastropoda...
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First thumbnail for: The genus Sveltia (Gastropoda, Cancellariidae) in ...
Second thumbnail for: The genus Sveltia (Gastropoda, Cancellariidae) in ...
Third thumbnail for: The genus Sveltia (Gastropoda, Cancellariidae) in ...
Journal Article
Published: 01 July 2007
Journal of Foraminiferal Research (2007) 37 (3): 204–212.
... neritea (Nassariidae) in France: evidence from mitochondrial sequence data : Molecular Ecology , v. 15 , p. 1699 – 1711 . Smith , L. D. , Wonham , M. J. , McCann , L. D. , Ruiz , G. M. , Hines , A. H. , and Carlton , J. T. , 1999 , Invasion pressure to a ballast...
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First thumbnail for: FIRST REPORT OF QUINQUELOCULINA CARINATASTRIATA ()...
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Journal Article
Journal: Paleobiology
Published: 01 August 2022
Paleobiology (2022) 48 (3): 462–479.
..., and predatory families per systems tract at the four stations. Station Systems tract Number of samples Prey Abundance (n > 20)* mollusks bivalves gastropods scaphopods Veneridae Cardiidae Rissoidae Cerithiidae Corbulidae Nassariidae Noetiidae Tellinidae...
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First thumbnail for: Scale dependence of drilling predation in the Holo...
Second thumbnail for: Scale dependence of drilling predation in the Holo...
Third thumbnail for: Scale dependence of drilling predation in the Holo...
Journal Article
Journal: PALAIOS
Published: 01 May 2011
PALAIOS (2011) 26 (5): 284–297.
.... In contrast, Neritidae (along with Naticidae) had the lowest PE in the Badenian, while Nassariidae had the highest, although their PE was very low at 0.8% ( Fig. 6 ). Drilling frequencies could fluctuate drastically within similar environments at single localities in the Central Paratethys ( Fig. 7...
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First thumbnail for: DRILLING PREDATION IN MOLLUSKS FROM THE LOWER AND ...
Second thumbnail for: DRILLING PREDATION IN MOLLUSKS FROM THE LOWER AND ...
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Published: 01 August 2022
gastropods scaphopods Veneridae Cardiidae Rissoidae Cerithiidae Corbulidae Nassariidae Noetiidae Tellinidae Brijuni lHST 5 905 509 393 3 90 112 117 115 38 7 19 1 eHST 14 7442 3883 3539 20 1160 702 900 780 210 72 407 18 MFZ 6 4834 2521 2310 3 941 307