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Journal articles on the topic 'Nautilus macromphalus'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Marie, Benjamin, Isabelle Zanella-Cléon, Marion Corneillat, Michel Becchi, Gérard Alcaraz, Laurent Plasseraud, Gilles Luquet, and Frédéric Marin. "Nautilin-63, a novel acidic glycoprotein from the shell nacre of Nautilus macromphalus." FEBS Journal 278, no. 12 (May 17, 2011): 2117–30. http://dx.doi.org/10.1111/j.1742-4658.2011.08129.x.

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2

Boucher-Rodoni, R., and G. Boucher. "Respiratory quotient and calcification of Nautilus macromphalus (Cephalopoda: Nautiloidea)." Marine Biology 117, no. 4 (December 1993): 629–33. http://dx.doi.org/10.1007/bf00349775.

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3

Ward, Peter Douglas. "Periodicity of chamber formation in chambered cephalopods: evidence from Nautilus macromphalus and Nautilus pompilius." Paleobiology 11, no. 4 (1985): 438–50. http://dx.doi.org/10.1017/s0094837300011726.

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The growth rates of ammonites and extinct nautiloids have been estimated in two ways: through analyses of shell growth lines and by analyzing the patterns of oxygen isotopic values from successive septa. In both types of studies, it has been assumed that the amount of time between successive chamber formation events is approximately constant. This assumption has never been tested with living cephalopods, however. To examine this, 10 immature Nautilus pompilius and two immature N. macromphalus were maintained in a surface aquarium for a period of 1 yr and periodically radiographed. The radiographs allowed direct observation of chamber formation events and apertural shell growth. During this observational period 61 separate chamber formation events were observed in the nautiluses. The time between separate chamber formation events increased in successively produced chambers, and varied from a minimum of 2–3 wk in a specimen of 45-mm shell diameter to a maximum of 13–15 wk in a specimen of 132-mm shell diameter. Unlike interval of chamber formation, which increased during ontogeny, rate of apertural shell growth showed no observable rate increase or decrease during ontogeny prior to maturity. With the onset of maturity, as marked by the shell characteristics defined by Collins et al. (1980), apertural shell growth rates dropped markedly, and ceased coincident with the removal of the last volumes of cameral liquid in the last formed, approximated chamber. Both rate of apertural shell growth and septal spacing were affected by degree of shell breakage.

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4

Pernice, Mathieu, Silke Wetzel, Olivier Gros, Renata Boucher-Rodoni, and Nicole Dubilier. "Enigmatic dual symbiosis in the excretory organ of Nautilus macromphalus (Cephalopoda: Nautiloidea)." Proceedings of the Royal Society B: Biological Sciences 274, no. 1614 (February 20, 2007): 1143–52. http://dx.doi.org/10.1098/rspb.2006.0353.

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Symbiosis is an important driving force in metazoan evolution and the study of ancient lineages can provide an insight into the influence of symbiotic associations on morphological and physiological adaptations. In the ‘living fossil’ Nautilus , bacterial associations are found in the highly specialized pericardial appendage. This organ is responsible for most of the excretory processes (ultrafiltration, reabsorption and secretion) and secretes an acidic ammonia-rich excretory fluid. In this study, we show that Nautilus macromphalus pericardial appendages harbour a high density of a β-proteobacterium and a coccoid spirochaete using transmission electron microscopy, comparative 16S rRNA sequence analysis and fluorescence in situ hybridization (FISH). These two bacterial phylotypes are phylogenetically distant from any known bacteria, with ammonia-oxidizing bacteria as the closest relatives of the β-proteobacterium (above or equal to 87.5% sequence similarity) and marine Spirochaeta species as the closest relatives of the spirochaete (above or equal to 89.8% sequence similarity), and appear to be specific to Nautilus . FISH analyses showed that the symbionts occur in the baso-medial region of the pericardial villi where ultrafiltration and reabsorption processes take place, suggesting a symbiotic contribution to the excretory metabolism.

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5

Westermann, B., and R. Schipp. "Morphology and histology of the digestive tract of Nautilus pompilius and Nautilus macromphalus (Cephalopoda, Tetrabranchiata)." Zoomorphology 117, no. 4 (February 4, 1998): 237–45. http://dx.doi.org/10.1007/s004350050048.

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6

Bustamante, P., S. Grigioni, R. Boucher-Rodoni, F. Caurant, and P. Miramand. "Bioaccumulation of 12 Trace Elements in the Tissues of the Nautilus Nautilus macromphalus from New Caledonia." Marine Pollution Bulletin 40, no. 8 (August 2000): 688–96. http://dx.doi.org/10.1016/s0025-326x(00)00005-9.

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7

SEUSS, BARBARA, DANIEL I. HEMBREE, MAX WISSHAK, ROYAL H. MAPES, and NEIL H. LANDMAN. "TAPHONOMY OF BACKSHORE VERSUS DEEP-MARINE COLLECTED NAUTILUS MACROMPHALUS CONCHS (NEW CALEDONIA)." PALAIOS 30, no. 7 (July 2015): 503–13. http://dx.doi.org/10.2110/palo.2014.057.

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8

Pernice, Mathieu, Julien Boucher, Renata Boucher-Rodoni, Pascale Joannot, and Paco Bustamante. "Comparative bioaccumulation of trace elements between Nautilus pompilius and Nautilus macromphalus (Cephalopoda: Nautiloidea) from Vanuatu and New Caledonia." Ecotoxicology and Environmental Safety 72, no. 2 (February 2009): 365–71. http://dx.doi.org/10.1016/j.ecoenv.2008.04.019.

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9

Dauphin, Yannicke. "Structure and composition of the septal nacreous layer of Nautilus macromphalus L. (Mollusca, Cephalopoda)." Zoology 109, no. 2 (May 2006): 85–95. http://dx.doi.org/10.1016/j.zool.2005.08.005.

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10

BUCKERIDGE, John, Tomáš KOČÍ, Ján SCHLÖGL, Adam TOMAŠOVÝCH, and Martina KOČOVÁ VESELSKÁ. "Deep‐water cirripedes colonizing dead shells of the cephalopod Nautilus macromphalus from New Caledonian waters." Integrative Zoology 14, no. 6 (November 2019): 561–75. http://dx.doi.org/10.1111/1749-4877.12389.

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11

Landman, Neil H., Royal H. Mapes, J. Kirk Cochran, Vincent Lignier, Daniel I. Hembree, Claire Goiran, Eric Folcher, and Philippe Brunet. "An Unusual Occurrence of Nautilus macromphalus in a Cenote in the Loyalty Islands (New Caledonia)." PLoS ONE 9, no. 12 (December 3, 2014): e113372. http://dx.doi.org/10.1371/journal.pone.0113372.

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12

Auclair, Anne-Cécile, Christophe Lecuyer, Hugo Bucher, and Simon M. F. Sheppard. "Carbon and oxygen isotope composition of Nautilus macromphalus: a record of thermocline waters off New Caledonia." Chemical Geology 207, no. 1-2 (June 2004): 91–100. http://dx.doi.org/10.1016/j.chemgeo.2004.02.006.

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13

Pernice, Mathieu, Delphine Pichon, Isabelle Domart-Coulon, Jocelyne Favet, and Renata Boucher-Rodoni. "Primary co-culture as a complementary approach to explore the diversity of bacterial associations in marine invertebrates: the example of Nautilus macromphalus (Cephalopoda: Nautiloidea)." Marine Biology 150, no. 5 (July 25, 2006): 749–57. http://dx.doi.org/10.1007/s00227-006-0413-2.

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14

Lafont, Anne-Gaëlle, Sylvie Dufour, and Martine Fouchereau-Peron. "Evidence for the Presence of Molecules Related to the Neuropeptide CGRP in Two Cephalopods, Sepia officinalis and Nautilus macromphalus: Comparison with Its Target Organ Distribution." Neuroendocrinology 84, no. 2 (2006): 138–50. http://dx.doi.org/10.1159/000097492.

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15

Boore, Jeffrey L. "The complete sequence of the mitochondrial genome of Nautilus macromphalus (Mollusca: Cephalopoda)." BMC Genomics 7, no. 1 (July 19, 2006). http://dx.doi.org/10.1186/1471-2164-7-182.

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16

"Correction: An Unusual Occurrence of Nautilus macromphalus in a Cenote in the Loyalty Islands (New Caledonia)." PLOS ONE 10, no. 3 (March 5, 2015): e0118532. http://dx.doi.org/10.1371/journal.pone.0118532.

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17

Marie, Benjamin, Nathalie Le Roy, Arul Marie, Lionel Dubost, Christian Milet, Laurent Bedouet, Michel Becchi, et al. "Nacre Evolution : A Proteomic Approach." MRS Proceedings 1187 (2009). http://dx.doi.org/10.1557/proc-1187-kk01-03.

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AbstractFrom an evolutionary viewpoint, the molluscan nacre constitutes a fascinating object. This microstructure appeared early, in the Lower Cambrian period, about 530 million years ago, and since then, has been kept unchanged until today. Nacre is restricted to the conchiferan mollusks, where it occurs in t least three main classes, bivalves, gastropods and cephalopods. The aim of the present study is to investigate whether all nacres are built from the same “macromolecular tools”, proteins of the nacre matrix. To this end, we studied three new nacre models, the freshwater bivalve Unio pictorum, the cephalopod Nautilus macromphalus, and the gastropod Haliotis asinina, to which we applied a combined biochemical and proteomic characterization of their respective nacre matrices. The results of our approach, that can be defined as “shellomics” (proteomics applied to shell proteins) shed a new light on the macroevolution of nacre matrix proteins and on the in vitro design of nacre-like biomaterials.

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