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Journal articles on the topic 'Latimeria chalumnae'

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Published: 4 June 2021
Last updated: 1 February 2022

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1

Forey, Peter L. "Latimeria chalumnae and its pedigree." Environmental Biology of Fishes 32, no. 1-4 (September 1991): 75–97. http://dx.doi.org/10.1007/bf00007446.

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2

Cupello, Camila, François J. Meunier, Marc Herbin, Gaël Clément, and Paulo M. Brito. "Lung anatomy and histology of the extant coelacanth shed light on the loss of air-breathing during deep-water adaptation in actinistians." Royal Society Open Science 4, no. 3 (March 2017): 161030. http://dx.doi.org/10.1098/rsos.161030.

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Lungs are specialized organs originated from the posterior pharyngeal cavity and considered as plesiomorphic for osteichthyans, as they are found in extant basal actinopterygians (i.e. Polypterus ) and in all major groups of extant sarcopterygians. The presence of a vestigial lung in adult stages of the extant coelacanth Latimeria chalumnae is the result of allometric growth during ontogeny, in relation with long-time adaptation to deep water. Here, we present the first detailed histological and anatomical description of the lung of Latimeria chalumnae , providing new insights into its arrested differentiation in an air-breathing complex, mainly represented by the absence of pneumocytes and of compartmentalization in the latest ontogenetic stages.
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3

FRITZSCH, B. "CommentaryThe ear of Latimeria chalumnae revisited." Zoology 106, no. 3 (2003): 243–48. http://dx.doi.org/10.1016/s0944-2006(04)70099-9.

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4

Forey, Peter L. "Golden jubilee for the coelacanth Latimeria chalumnae." Nature 336, no. 6201 (December 1988): 727–32. http://dx.doi.org/10.1038/336727a0.

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5

Hissmann, Karen, Hans Fricke, and Jürgen Schauer. "Population Monitoring of the Coelacanth (Latimeria chalumnae)." Conservation Biology 12, no. 4 (July 7, 2008): 759–65. http://dx.doi.org/10.1111/j.1523-1739.1998.97060.x.

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6

Hissmann, Karen, Hans Fricke, and Jurgen Schauer. "Population Monitoring of the Coelacanth (Latimeria chalumnae)." Conservation Biology 12, no. 4 (August 24, 1998): 759–65. http://dx.doi.org/10.1046/j.1523-1739.1998.97060.x.

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7

Bruton, Michael N., and Michael J. Armstrong. "The demography of the coelacanth Latimeria chalumnae." Environmental Biology of Fishes 32, no. 1-4 (September 1991): 301–11. http://dx.doi.org/10.1007/bf00007463.

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8

Smith, Moya Meredith, M. H. Hobdell, and W. A. Miller. "The structure of the scales of Latimeria chalumnae." Journal of Zoology 167, no. 4 (August 20, 2009): 501–9. http://dx.doi.org/10.1111/j.1469-7998.1972.tb01741.x.

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9

Bemis, William E., and R. Glenn Northcutt. "Innervation of the basicranial muscle of Latimeria chalumnae." Environmental Biology of Fishes 32, no. 1-4 (September 1991): 147–58. http://dx.doi.org/10.1007/bf00007450.

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10

Thoney, Dennis A., and William J. Hargis. "Juvenile anisakine parasites from the coelacanth Latimeria chalumnae." Environmental Biology of Fishes 32, no. 1-4 (September 1991): 281–83. http://dx.doi.org/10.1007/bf00007461.

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11

Mattei, Xavier, Yves Siau, and Bernard Seret. "Etude ultrastructurale du spermatozoïde du coelacanthe: Latimeria chalumnae." Journal of Ultrastructure and Molecular Structure Research 101, no. 2-3 (November 1988): 243–51. http://dx.doi.org/10.1016/0889-1605(88)90015-8.

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12

Maisey, John G., John A. Musick, Michael K. Bruton, and Eugene K. Balon. "The Biology of Latimeria Chalumnae and Evolution of Coelacanths." Copeia 1992, no. 3 (August 18, 1992): 926. http://dx.doi.org/10.2307/1446177.

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13

Bruton, Michael N., and Robin E. Stobbs. "The ecology and conservation of the coelacanth Latimeria chalumnae." Environmental Biology of Fishes 32, no. 1-4 (September 1991): 313–39. http://dx.doi.org/10.1007/bf00007464.

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14

Anderson, Roy C. "LarvalAnisakis sp. (Ascaridoidea, Anisakidae) from the coelacanth,Latimeria chalumnae." Environmental Biology of Fishes 38, no. 4 (December 1993): 411–13. http://dx.doi.org/10.1007/bf00007537.

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15

Sasaki, Takeshi, Tetsu Sato, Seiko Miura, Philip O. J. Bwathondi, Benjamin P. Ngatunga, and Norihiro Okada. "Mitogenomic analysis for coelacanths (Latimeria chalumnae) caught in Tanzania." Gene 389, no. 1 (March 2007): 73–79. http://dx.doi.org/10.1016/j.gene.2006.09.021.

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16

Cloutier, Richard, Hans-Peter Schultze, Edward O. Wiley, John A. Musick, John C. Daimler, Mark A. Brown, Samuel J. Dwyer, Larry T. Cook, and Richard L. Laws. "Recent radiologic imaging techniques for morphological studies in Latimeria chalumnae." Environmental Biology of Fishes 23, no. 4 (December 1988): 281–82. http://dx.doi.org/10.1007/bf00005239.

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17

Schultze, Hans-Peter, and Richard Cloutier. "Computed tomography and magnetic resonance imaging studies of Latimeria chalumnae." Environmental Biology of Fishes 32, no. 1-4 (September 1991): 159–81. http://dx.doi.org/10.1007/bf00007451.

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18

Schultze, Hans-Peter. "CT scan reconstruction of the palate region of Latimeria chalumnae." Environmental Biology of Fishes 32, no. 1-4 (September 1991): 183–92. http://dx.doi.org/10.1007/bf00007452.

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19

Uyeno, Teruya. "Observations on locomotion and feeding of released coelacanths, Latimeria chalumnae." Environmental Biology of Fishes 32, no. 1-4 (September 1991): 267–73. http://dx.doi.org/10.1007/bf00007459.

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20

Thornycroft, Rosanne E., and Anthony J. Booth. "Computer-aided identification of coelacanths,Latimeria chalumnae, using scale patterns." Marine Biology Research 8, no. 3 (April 2012): 300–306. http://dx.doi.org/10.1080/17451000.2011.628679.

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21

Bernstein, Peter. "The ear region of Latimeria chalumnae: functional and evolutionary implications." Zoology 106, no. 3 (January 2003): 233–42. http://dx.doi.org/10.1078/0944-2006-00119.

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22

Fricke, Hans, Olaf Reinicke, Heribert Hofer, and Werner Nachtigall. "Locomotion of the coelacanth Latimeria chalumnae in its natural environment." Nature 329, no. 6137 (September 1987): 331–33. http://dx.doi.org/10.1038/329331a0.

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23

Fricke, H., and K. Hissmann. "Home range and migrations of the living coelacanth Latimeria chalumnae." Marine Biology 120, no. 2 (September 1994): 171–80. http://dx.doi.org/10.1007/bf00349676.

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24

Tamai, Yoichi, Hisako Kojima, and Kumiko Abe. "Chemical characterization of the brain of a coelacanth, Latimeria chalumnae." Comparative Biochemistry and Physiology Part B: Comparative Biochemistry 83, no. 2 (January 1986): 295–99. http://dx.doi.org/10.1016/0305-0491(86)90369-x.

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25

Yokoyama, S., H. Zhang, F. B. Radlwimmer, and N. S. Blow. "Adaptive evolution of color vision of the Comoran coelacanth (Latimeria chalumnae)." Proceedings of the National Academy of Sciences 96, no. 11 (May 25, 1999): 6279–84. http://dx.doi.org/10.1073/pnas.96.11.6279.

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26

Setter, Ann L., and George W. Brown. "Enzymes of the coelacanth Latimeria chalumnae evidenced by starch gel electrophoresis." Environmental Biology of Fishes 32, no. 1-4 (September 1991): 193–98. http://dx.doi.org/10.1007/bf00007453.

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27

Wourms, John P., James W. Atz, and M. Dean Stribling. "Viviparity and the maternal-embryonic relationship in the coelacanth Latimeria chalumnae." Environmental Biology of Fishes 32, no. 1-4 (September 1991): 225–48. http://dx.doi.org/10.1007/bf00007456.

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28

Hale, Robert C., John Greaves, Jennifer L. Gundersen, and Robert F. Mothershead. "Occurrence of organochlorine contaminants in tissues of the coelacanth Latimeria chalumnae." Environmental Biology of Fishes 32, no. 1-4 (September 1991): 361–67. http://dx.doi.org/10.1007/bf00007466.

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29

Betz, U. A., W. E. Mayer, and J. Klein. "Major histocompatibility complex class I genes of the coelacanth Latimeria chalumnae." Proceedings of the National Academy of Sciences 91, no. 23 (November 8, 1994): 11065–69. http://dx.doi.org/10.1073/pnas.91.23.11065.

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30

Fricke, H., and K. Hissmann. "Feeding ecology and evolutionary survival of the living coelacanth Latimeria chalumnae." Marine Biology 136, no. 2 (March 28, 2000): 379–86. http://dx.doi.org/10.1007/s002270050697.

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31

Challands, T. J., Jason D. Pardo, and Alice M. Clement. "Mandibular musculature constrains brain–endocast disparity between sarcopterygians." Royal Society Open Science 7, no. 9 (September 2020): 200933. http://dx.doi.org/10.1098/rsos.200933.

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The transition from water to land by the earliest tetrapods in the Devonian Period is seen as one of the greatest steps in evolution. However, little is understood concerning changes in brain morphology over this transition. Here, we determine the brain–braincase relationship in fishes and basal lissamphibians as a proxy to elucidate the changes that occurred over the fish–tetrapod transition. We investigate six basal extant sarcopterygians spanning coelacanths to salamanders ( Latimeria chalumnae, Neoceratodus, Protopterus aethiopicus, P. dolloi, Cynops, Ambystoma mexicanum ) using micro-CT and MRI and quantify the brain–braincase relationship in these extant taxa. Our results show that regions of lowest brain–endocast disparity are associated with regions of bony reinforcement directly adjacent to masticatory musculature for the mandible except in Neoceratodus and Latimeria . In Latimeria this deviation from the trend can be accounted for by the possession of an intracranial joint and basicranial muscles, whereas in Neoceratodus difference is attributed to dermal bones contributing to the overall neurocranial reinforcement. Besides Neoceratodus and Latimeria, regions of low brain–endocast disparity occur where there is less reinforcement away from high mandibular muscle mass, where the trigeminal nerve complex exits the braincase and where endolymphatic sacs occupy space between the brain and braincase wall. Despite basal tetrapods possessing reduced adductor muscle mass and a different biting mechanism to piscine sarcopterygians, regions of the neurocranium lacking osteological reinforcement in the basal tetrapods Lethiscus and Brachydectes broadly correspond to regions of high brain–endocast disparity seen in extant taxa.
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32

Fricke, Hans, and Karen Hissmann. "Locomotion, fin coordination and body form of the living coelacanth Latimeria chalumnae." Environmental Biology of Fishes 34, no. 4 (August 1992): 329–56. http://dx.doi.org/10.1007/bf00004739.

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33

Waehneldt, Thomas V., Joachim Malotka, Gunnar Jeserich, and Jean-Marie Matthieu. "Central nervous system myelin proteins of the coelacanth Latimeria chalumnae: phylogenetic implications." Environmental Biology of Fishes 32, no. 1-4 (September 1991): 131–43. http://dx.doi.org/10.1007/bf00007449.

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34

Uyeno, Teruya, and Toshio Tsutsumi. "Stomach contents of Latimeria chalumnae and further notes on its feeding habits." Environmental Biology of Fishes 32, no. 1-4 (September 1991): 275–79. http://dx.doi.org/10.1007/bf00007460.

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35

Fricke, Hans, Karen Hissmann, J�rgen Schauer, Olaf Reinicke, Lutz Kasang, and Raphael Plante. "Habitat and population size of the coelacanth Latimeria chalumnae at Grand Comoro." Environmental Biology of Fishes 32, no. 1-4 (September 1991): 287–300. http://dx.doi.org/10.1007/bf00007462.

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36

Bruton, Michael N., Sheila E. Coutouvidis, and Jean Pote. "Bibliography of the living coelacanth Latimeria chalumnae, with comments on publication trends." Environmental Biology of Fishes 32, no. 1-4 (September 1991): 403–33. http://dx.doi.org/10.1007/bf00007469.

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37

Hughes, George M. "The gills of the coelacanth,Latimeria chalumnae Latimeriidae.What can they teach us?" Italian Journal of Zoology 65, sup1 (January 1998): 425–29. http://dx.doi.org/10.1080/11250009809386859.

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38

Huby, Alessia, Rohan Mansuit, Marc Herbin, and Anthony Herrel. "Revision of the muscular anatomy of the paired fins of the living coelacanth Latimeria chalumnae (Sarcopterygii: Actinistia)." Biological Journal of the Linnean Society 133, no. 4 (April 30, 2021): 949–89. http://dx.doi.org/10.1093/biolinnean/blab047.

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Abstract As a sarcopterygian fish, the extant coelacanth Latimeria has muscular paired fins, different in their skeletal and muscular anatomy from the paired fins of actinopterygians. Although the muscular anatomy of the pectoral and pelvic fins of Latimeria has been described by several studies, a detailed functional description of the muscles and their architecture has never been performed. Our detailed functional description of the muscles of the paired fins shows a more complex organization than previously described. The pectoral and pelvic fins have a different organization of their muscular anatomy, and the pelvic fin shows a more plesiomorphic configuration of the muscles since most of them are poly-articular and run from the pelvic girdle to the fin rays, an organization typical of actinopterygians. We found that the pectoral fins are stronger than the pelvic fins which is likely to be associated with the greater contribution of the pectoral fins to locomotion and manoeuvring. Finally, the study of the joint mobility of the paired fins showed that the pectoral fins show greater mobility than the pelvic fins. The reduced mobility of the pelvic fin is possibly a consequence of the morphology of the mesomeres and the large pre-axial radials.
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39

Amemiya, C. T., Y. Ohta, R. T. Litman, J. P. Rast, R. N. Haire, and G. W. Litman. "VH gene organization in a relict species, the coelacanth Latimeria chalumnae: evolutionary implications." Proceedings of the National Academy of Sciences 90, no. 14 (July 15, 1993): 6661–65. http://dx.doi.org/10.1073/pnas.90.14.6661.

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40

Fricke, H., and R. Plante. "Habitat requirements of the living coelacanth Latimeria chalumnae at grande comore, Indian Ocean." Naturwissenschaften 75, no. 3 (March 1988): 149–51. http://dx.doi.org/10.1007/bf00405310.

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41

Stock, David W., Kirk D. Moberg, Linda R. Maxson, and Gregory S. Whitt. "A phylogenetic analysis of the 18S ribosomal RNA sequence of the coelacanth Latimeria chalumnae." Environmental Biology of Fishes 32, no. 1-4 (September 1991): 99–117. http://dx.doi.org/10.1007/bf00007447.

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42

Hissmann, K., H. Fricke, and J. Schauer. "Patterns of time and space utilisation in coelacanths ( Latimeria chalumnae ), determined by ultrasonic telemetry." Marine Biology 136, no. 5 (June 16, 2000): 943–52. http://dx.doi.org/10.1007/s002270000294.

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43

Yabumoto, Yoshitaka, Masamitu Iwata, Yoshitaka Abe, and Teruya Uyeno. "Function of the pseudomaxillary fold in the mouth opening of the coelacanth, Latimeria chalumnae." Ichthyological Research 59, no. 2 (January 27, 2012): 164–68. http://dx.doi.org/10.1007/s10228-011-0267-6.

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44

Yellan, Isaac, Ally W. H. Yang, and Timothy R. Hughes. "Diverse Eukaryotic CGG-Binding Proteins Produced by Independent Domestications of hAT Transposons." Molecular Biology and Evolution 38, no. 5 (February 9, 2021): 2070–75. http://dx.doi.org/10.1093/molbev/msab007.

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Abstract The human transcription factor (TF) CGGBP1 (CGG-binding protein) is conserved only in amniotes and is believed to derive from the zf-BED and Hermes transposase DNA-binding domains (DBDs) of a hAT DNA transposon. Here, we show that sequence-specific DNA-binding proteins with this bipartite domain structure have resulted from dozens of independent hAT domestications in different eukaryotic lineages. CGGBPs display a wide range of sequence specificity, usually including preferences for CGG or CGC trinucleotides, whereas some bind AT-rich motifs. The CGGBPs are almost entirely nonsyntenic, and their protein sequences, DNA-binding motifs, and patterns of presence or absence in genomes are uncharacteristic of ancestry via speciation. At least eight CGGBPs in the coelacanth Latimeria chalumnae bind distinct motifs, and the expression of the corresponding genes varies considerably across tissues, suggesting tissue-restricted function.
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45

Boord, R. L., R. Glenn Northcutt, and William E. Bemis. "Cranial Nerves of the Coelacanth Latimeria Chalumnae (Osteichthyes: Sarcopterygii: Actinistia) and Comparisons with Other Craniata." Copeia 1994, no. 3 (August 17, 1994): 828. http://dx.doi.org/10.2307/1447206.

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46

Smith, Moya M. "Enamel in the oral teeth of Latimeria chalumnae (Pisces: Actinistia): a scanning electron microscope study." Journal of Zoology 185, no. 3 (August 20, 2009): 355–69. http://dx.doi.org/10.1111/j.1469-7998.1978.tb03338.x.

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47

Gao, Bo, Yatong Sang, Wencheng Zong, Mohamed Diaby, Dan Shen, Saisai Wang, Yali Wang, Cai Chen, and Chengyi Song. "Evolution and domestication of Tc1/mariner transposons in the genome of African coelacanth (Latimeria chalumnae)." Genome 63, no. 8 (August 2020): 375–86. http://dx.doi.org/10.1139/gen-2019-0216.

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Here, we comprehensively analysed the abundance, diversity, and activity of Tc1/mariner transposons in African coelacanth (Latimeria chalumnae). Fifteen Tc1/mariner autonomous transposons were identified and grouped into six clades: DD34E/Tc1, DD34D/mariner, DD35D/Fot, DD31D/pogo, DD30-31D/pogo-like, and DD32–36D/Tigger, belonging to three known families: DD34E/Tc1, DD34D/mariner, and DD×D/pogo (DD35D/Fot, DD31D/pogo, DD30-31D/pogo-like, and DD32-36D/Tigger). Thirty-one miniature inverted-repeat transposable element (MITE) transposons of Tc1/mariner were also identified, and 20 of them display similarity to the identified autonomous transposons. The structural organization of these full Tc1/mariner elements includes a transposase gene flanked by terminal inverted repeats (TIRs) with TA dinucleotides. The transposases contain N-terminal DNA binding domain and a C-terminal catalytic domain characterized by the presence of a conservative D(Asp)DE(Glu)/D triad that is essential for transposase activity. The Tc1/mariner superfamily in coelacanth exhibited very low genome coverage (0.3%), but it experienced an extraordinary difference of proliferation dynamics among the six clades identified; moreover, most of them exhibited a very recent and current proliferation, suggesting that some copies of these transposons are putatively active. Additionally, at least four functional genes derived from Tc1/mariner transposons were found. We provide an up-to-date overview of Tc1/mariner in coelacanth, which may be helpful in determining genome and gene evolution in this living fossil.
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48

Coro, Gianpaolo, Pasquale Pagano, and Anton Ellenbroek. "Combining simulated expert knowledge with Neural Networks to produce Ecological Niche Models for Latimeria chalumnae." Ecological Modelling 268 (October 2013): 55–63. http://dx.doi.org/10.1016/j.ecolmodel.2013.08.005.

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49

Meunier, F. J., J. Mondéjar-Fernández, F. Goussard, G. Clément, and M. Herbin. "Presence of plicidentine in the oral teeth of the coelacanth Latimeria chalumnae Smith 1939 (Sarcopterygii; Actinistia)." Journal of Structural Biology 190, no. 1 (April 2015): 31–37. http://dx.doi.org/10.1016/j.jsb.2015.02.005.

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50

Hillis, David M., Michael T. Dixon, and Loren K. Ammerman. "The relationships of the coelacanth Latimeria chalumnae: evidence from sequences of vertebrate 28S ribosomal RNA genes." Environmental Biology of Fishes 32, no. 1-4 (September 1991): 119–30. http://dx.doi.org/10.1007/bf00007448.

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