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Journal articles on the topic 'Butterflyfishes'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

Noonan, Kara R., and Michael J. Childress. "Association of butterflyfishes and stony coral tissue loss disease in the Florida Keys." Coral Reefs 39, no. 6 (2020): 1581–90. http://dx.doi.org/10.1007/s00338-020-01986-8.

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AbstractSince 2014, stony coral tissue loss disease (SCTLD) has rapidly spread throughout the Florida reef tract infecting and killing dozens of coral species. Previous studies have found that corallivorous fishes, such as butterflyfishes, are positively correlated with coral disease prevalence at both local and regional scales. This study investigates the association of SCTLD infection and butterflyfish abundance and behaviors on ten reefs in the middle Florida Keys. Divers conducted video surveys of reef fish abundance and disease prevalence in June 2017, 2018, and 2019; before, during, and

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2

Leahy, Susannah M., Garry R. Russ, and Rene A. Abesamis. "Primacy of bottom-up effects on a butterflyfish assemblage." Marine and Freshwater Research 67, no. 8 (2016): 1175. http://dx.doi.org/10.1071/mf15012.

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The question of whether biological systems are maintained by top-down versus bottom-up drivers is a recurring one in ecology. It is a particularly important question to address in the management of coral reefs, which are at risk from a variety of anthropogenic stressors. Here, we explicitly test whether the abundance of different feeding guilds of coral-associated Chaetodon butterflyfishes are controlled by top-down or bottom-up drivers, and we assess the relative influence of all statistically significant drivers. We find that the abundance and species richness of Chaetodon butterflyfishes ar

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3

REVERTER, MIRIAM, SCOTT C. CUTMORE, RODNEY BRAY, THOMAS H. CRIBB, and PIERRE SASAL. "Gill monogenean communities (Platyhelminthes, Monogenea, Dactylogyridae) of butterflyfishes from tropical Indo-West Pacific Islands." Parasitology 143, no. 12 (2016): 1580–91. http://dx.doi.org/10.1017/s0031182016001463.

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SUMMARYWe studied the monogenean communities of 34 species of butterflyfish from the tropical Indo-West Pacific, identifying 13 dactylogyrid species (including two species that are presently undescribed). Monogenean assemblages differed significantly between host species in terms of taxonomic structure, intensity and prevalence. Parasite richness ranged from 0 (Chaetodon lunulatus) to 11 (C. auriga, C. citrinellus and C. lunula). Host specificity varied between the dactylogyrids species, being found on 2–29 of the 34 chaetodontid species examined. Sympatric butterflyfish species were typically

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4

Righton, David, Jeremy Kemp, and Rupert Ormond. "Biogeography, Community Structure and Diversity of Red Sea and Western Indian Ocean Butterflyfishes." Journal of the Marine Biological Association of the United Kingdom 76, no. 1 (1996): 223–28. http://dx.doi.org/10.1017/s0025315400029167.

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Patterns of variation in the assemblage structure of butterflyfishes (Chaetodontidae) of the Red Sea and western Indian Ocean have been compared. There is a lower number of species in the Red Sea, a high proportion of which are endemic to the region, both features that have been attributed to the relatively recent origin of the Red Sea. In the Red Sea overall mean abundance of butterflyfish is greatest in the central part, decreasing both to north and south. Several species present in the southern Red Sea are absent from the north. By contrast, most western Indian Ocean species are widely dist

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5

Faricha, Ana, Isa N. Edrus, Sasanti R. Suharti, et al. "Relationship Between Species Composition of Butterflyfishes and Coral Cover (Study case: Taka Bonerate National Park)." ILMU KELAUTAN: Indonesian Journal of Marine Sciences 25, no. 3 (2020): 121–26. http://dx.doi.org/10.14710/ik.ijms.25.3.121-126.

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The coral reef environment has a strong influence on associated organisms such as fishes, mollusks, and others. Wherein, the butterflyfishes are marine fishes which closely associated with the tropic group as dietary specialization i.e. obligate coral feeder, facultative, and generalist. The obligate may respond only to change in preferred corals and not indicate others. However, generalist show in different response in habitat deteriorates and may allow switching feeding to a less preferred one. Many questions remain about food specific at the species level which may potentially as bio-indica

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6

Cole, A. J., R. J. Lawton, M. S. Pratchett, and S. K. Wilson. "Chronic coral consumption by butterflyfishes." Coral Reefs 30, no. 1 (2010): 85–93. http://dx.doi.org/10.1007/s00338-010-0674-6.

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7

Bauchot, Roland, Jean-Marc Ridet, and Marie-Louise Bauchot. "The brain organization of butterflyfishes." Environmental Biology of Fishes 25, no. 1-3 (1989): 205–19. http://dx.doi.org/10.1007/bf00002213.

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8

Nowicki, Jessica P., Morgan S. Pratchett, Stefan P. W. Walker, Darren J. Coker, and Lauren A. O'Connell. "Gene expression correlates of social evolution in coral reef butterflyfishes." Proceedings of the Royal Society B: Biological Sciences 287, no. 1929 (2020): 20200239. http://dx.doi.org/10.1098/rspb.2020.0239.

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Animals display remarkable variation in social behaviour. However, outside of rodents, little is known about the neural mechanisms of social variation, and whether they are shared across species and sexes, limiting our understanding of how sociality evolves. Using coral reef butterflyfishes, we examined gene expression correlates of social variation (i.e. pair bonding versus solitary living) within and between species and sexes. In several brain regions, we quantified gene expression of receptors important for social variation in mammals: oxytocin ( OTR ), arginine vasopressin ( V1aR ), dopami

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9

Gürsoy, Derya. "Taxonomic Update on Coral Reef Butterflyfishes: Implications for Conservation." FishTaxa 32 (April 22, 2024): 11–20. https://doi.org/10.5281/zenodo.14706193.

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10

Pratchett, M. S., M. L. Berumen, M. J. Marnane, J. V. Eagle, and D. J. Pratchett. "Habitat associations of juvenile versus adult butterflyfishes." Coral Reefs 27, no. 3 (2008): 541–51. http://dx.doi.org/10.1007/s00338-008-0357-8.

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11

Tricas, Timothy C., and Kelly S. Boyle. "Acoustico‐lateralis communication in coral reef butterflyfishes." Journal of the Acoustical Society of America 120, no. 5 (2006): 3104. http://dx.doi.org/10.1121/1.4787561.

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12

Driscoll, Janis Wiley, and John L. Driscoll. "Pair behavior and spacing in butterflyfishes (Chaetodontidae)." Environmental Biology of Fishes 22, no. 1 (1988): 29–37. http://dx.doi.org/10.1007/bf00000542.

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13

Alfaro, Michael E., Elizabeth A. Karan, Shawn T. Schwartz, and Allison J. Shultz. "The Evolution of Color Pattern in Butterflyfishes (Chaetodontidae)." Integrative and Comparative Biology 59, no. 3 (2019): 604–15. http://dx.doi.org/10.1093/icb/icz119.

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Abstract Coral reef fishes constitute one of the most diverse assemblages of vertebrates on the planet. Color patterns are known to serve a number of functions including intra- and inter-specific signaling, camouflage, mimicry, and defense. However, the relative importance of these and other factors in shaping color pattern evolution is poorly understood. Here we conduct a comparative phylogenetic analysis of color pattern evolution in the butterflyfishes (Chaetodontidae). Using recently developed tools for quantifying color pattern geometry as well as machine learning approaches, we investiga

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14

Climaco, Russell, Geofrey Aludia, Niño Jess Mar Mecha, et al. "Status of coral reefs, butterflyfishes, and benthic macro-invertebrates in Araceli and Dumaran, Palawan, Philippines." Palawan Scientist 14, no. 2 (2022): 54–64. http://dx.doi.org/10.69721/tps.j.2022.14.2.07.

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As a major fishing ground in Palawan, the reefs in the municipal waters of Araceli and Dumaran are continuously facing anthropogenic and climate-related threats. Hence, to provide information about the reef conditions, surveys were undertaken in three sites of each municipality as the basis for management. Data collection used the C30 method where a 75 m x 25 m sampling area was established at the upper reef slope (2-5 m deep) of each site. Substrates were photo-documented at predetermined random positions and the photos were processed using Coral Point Count with excel extension software (CPC

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15

Tricas, Timothy C., and Kelly Boyle. "Sound production and hearing in coral reef butterflyfishes." Journal of the Acoustical Society of America 125, no. 4 (2009): 2487. http://dx.doi.org/10.1121/1.4783295.

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16

Righton, D. "Territorial and foraging behaviour of two corallivorous butterflyfishes." Journal of Fish Biology 63 (December 2003): 239–40. http://dx.doi.org/10.1111/j.1095-8649.2003.216ae.x.

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17

Montanari, Stefano R., Lynne van Herwerden, Morgan S. Pratchett, Jean-Paul A. Hobbs, and Anneli Fugedi. "Reef fish hybridization: lessons learnt from butterflyfishes (genusChaetodon)." Ecology and Evolution 2, no. 2 (2011): 310–28. http://dx.doi.org/10.1002/ece3.83.

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18

Nanami, Atsushi. "Spatial distribution and feeding substrate of butterflyfishes (family Chaetodontidae) on an Okinawan coral reef." PeerJ 8 (August 4, 2020): e9666. http://dx.doi.org/10.7717/peerj.9666.

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Coral reefs support diverse communities, and relationships among organisms within these communities are quite complex. Among the relationships, clarifying the habitat association and foraging substrate selection relative to habitat characteristics is of central importance to ecology since these two aspects are the fundamentals for survival and growth of organisms. The aims of the present study were to investigate the spatial distribution and feeding substrate selection of 14 species of butterflyfishes on an Okinawan coral reef in Japan. Species-specific spatial distributions varied with habita

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19

Cole, A. J., and M. S. Pratchett. "Effects of juvenile coral-feeding butterflyfishes on host corals." Coral Reefs 30, no. 3 (2011): 623–30. http://dx.doi.org/10.1007/s00338-011-0746-2.

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20

Berumen, M. L., M. S. Pratchett, and B. A. Goodman. "Relative gut lengths of coral reef butterflyfishes (Pisces: Chaetodontidae)." Coral Reefs 30, no. 4 (2011): 1005–10. http://dx.doi.org/10.1007/s00338-011-0791-x.

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21

Hobbs, Jean-Paul A., and Maya Srinivasan. "Structure of Reef Fish Families (Butterflyfishes and Angelfishes) at Isolated Oceanic Reefs in the Indian Ocean: Christmas Island and the Cocos (Keeling) Islands." Diversity 16, no. 9 (2024): 569. http://dx.doi.org/10.3390/d16090569.

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There has been substantial research on the factors that structure reef fish assemblages, but this has mostly focused on nearshore or continental reefs. This study examines patterns of abundance and species composition for two iconic groups of coral reef fishes, angelfishes (family Pomacanthidae) and butterflyfishes (family Chaetodontidae) at two isolated, oceanic reefs in the Indian Ocean: Christmas Island and the Cocos (Keeling) Islands. Six explanatory variables were investigated to determine whether large-scale physical factors are more important than fine-scale biotic factors in structurin

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22

Nanami, Atsushi. "Nocturnal substrate association of four coral reef fish groups (parrotfishes, surgeonfishes, groupers and butterflyfishes) in relation to substrate architectural characteristics." PeerJ 12 (July 19, 2024): e17772. http://dx.doi.org/10.7717/peerj.17772.

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Although numerous coral reef fish species utilize substrates with high structural complexities as habitats and refuge spaces, quantitative analysis of nocturnal fish substrate associations has not been sufficiently examined yet. The aims of the present study were to clarify the nocturnal substrate associations of 17 coral reef fish species (nine parrotfish, two surgeonfish, two grouper and four butterflyfish) in relation to substrate architectural characteristics. Substrate architectural characteristics were categorized into seven types: (1) eave-like space, (2) large inter-branch space, (3) o

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23

Nagelkerken, I., G. van der Velde, S. L. J. Wartenbergh, M. M. Nugues, and M. S. Pratchett. "Cryptic dietary components reduce dietary overlap among sympatric butterflyfishes (Chaetodontidae)." Journal of Fish Biology 75, no. 6 (2009): 1123–43. http://dx.doi.org/10.1111/j.1095-8649.2009.02303.x.

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24

Kelley, Jennifer L., John L. Fitzpatrick, and Sami Merilaita. "Spots and stripes: ecology and colour pattern evolution in butterflyfishes." Proceedings of the Royal Society B: Biological Sciences 280, no. 1757 (2013): 20122730. http://dx.doi.org/10.1098/rspb.2012.2730.

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25

Lawton, Rebecca J., Andrew J. Cole, Michael L. Berumen, and Morgan S. Pratchett. "Geographic variation in resource use by specialist versus generalist butterflyfishes." Ecography 35, no. 6 (2011): 566–76. http://dx.doi.org/10.1111/j.1600-0587.2011.07326.x.

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26

McMillan, W. Owen, and Stephen R. Palumbi. "Rapid Rate of Control-Region Evolution in Pacific Butterflyfishes (Chaetodontidae)." Journal of Molecular Evolution 45, no. 5 (1997): 473–84. http://dx.doi.org/10.1007/pl00006252.

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27

Pratchett, M. S., S. A. Blowes, D. Coker, E. Kubacki, J. Nowicki, and A. S. Hoey. "Indirect benefits of high coral cover for non-corallivorous butterflyfishes." Coral Reefs 34, no. 2 (2014): 665–72. http://dx.doi.org/10.1007/s00338-014-1254-y.

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28

Lecchini, David, Suzanne C. Mills, Christophe Brié, Cedrik M. Lo, and Bernard Banaigs. "Chemical stimuli in coral reefs: how butterflyfishes find their food." Environmental Biology of Fishes 91, no. 3 (2011): 303–9. http://dx.doi.org/10.1007/s10641-011-9785-3.

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29

Clark, Nicholas J., and Garry R. Russ. "Ontogenetic shifts in the habitat associations of butterflyfishes (F. Chaetodontidae)." Environmental Biology of Fishes 94, no. 4 (2012): 579–90. http://dx.doi.org/10.1007/s10641-011-9964-2.

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30

Colin, Patrick L. "Aspects of the spawning of western Atlantic butterflyfishes (Pisces: Chaetodontidae)." Environmental Biology of Fishes 25, no. 1-3 (1989): 131–41. http://dx.doi.org/10.1007/bf00002207.

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31

Blowes, Shane A., Morgan S. Pratchett, and Sean R. Connolly. "Aggression, interference, and the functional response of coral-feeding butterflyfishes." Oecologia 184, no. 3 (2017): 675–84. http://dx.doi.org/10.1007/s00442-017-3902-8.

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32

Ferry-Graham, Lara A., Peter C. Wainwright, C. Darrin Hulsey, and David R. Bellwood. "Evolution and mechanics of long jaws in butterflyfishes (Family Chaetodontidae)." Journal of Morphology 248, no. 2 (2001): 120–43. http://dx.doi.org/10.1002/jmor.1024.

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33

Mendoza-Franco, Edgar F., Nuno Simões, Víctor M. Vidal-Martínez, and María L. Aguirre-Macedo. "Rediscovering Monogenoids (Platyhelminthes) Parasitizing Pomacentrid and Chaetodontid Fishes from Cayo Arcas Reef, Gulf of Mexico." Diversity 14, no. 11 (2022): 985. http://dx.doi.org/10.3390/d14110985.

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During a research of gill ectoparasites on damselfishes (Pomacentridae) and butterflyfishes (Chaetodontidae) from the Cayo Arcas reef in the Campeche Bank (Gulf of Mexico), the following monogenoids (Platyhelminthes) were found: Paraeuryhaliotrema pomacentris n. gen., n. sp. (Dactylogyridae) on beaugregory Stegastes xanthurus (Poey, 1860) (Pomacentridae) that is characterized, in part, by possessing a haptor armed with a dorsal, ventral anchor-bar complexes, seven pairs of similar hooks; two pairs of eyespots; overlapping gonads; a copulatory complex composed of a male copulatory organ (MCO) a

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34

Konow, Nicolai, Samantha Price, Richard Abom, David Bellwood, and Peter Wainwright. "Decoupled diversification dynamics of feeding morphology following a major functional innovation in marine butterflyfishes." Proceedings of the Royal Society B: Biological Sciences 284, no. 1860 (2017): 20170906. http://dx.doi.org/10.1098/rspb.2017.0906.

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The diversity of fishes on coral reefs is influenced by the evolution of feeding innovations. For instance, the evolution of an intramandibular jaw joint has aided shifts to corallivory in Chaetodon butterflyfishes following their Miocene colonization of coral reefs. Today, over half of all Chaetodon species consume coral, easily the largest concentration of corallivores in any reef fish family. In contrast with Chaetodon , other chaetodontids, including the long-jawed bannerfishes, remain less intimately associated with coral and mainly consume other invertebrate prey. Here, we test (i) if in

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35

Alwany, Magdy A., Salah G. El-Etreby, and Mahmoud H. Hanafy. "Distribution and Abundance of Butterflyfishes Along the Gulf of Aqaba, Egypt." Journal of Fisheries and Aquatic Science 2, no. 6 (2007): 395–402. http://dx.doi.org/10.3923/jfas.2007.395.402.

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36

Webb, J. F., J. L. Herman, C. F. Woods, and D. R. Ketten. "The ears of butterflyfishes (Chaetodontidae): ‘hearing generalists' on noisy coral reefs?" Journal of Fish Biology 77, no. 6 (2010): 1406–23. http://dx.doi.org/10.1111/j.1095-8649.2010.02765.x.

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37

Leis, Jeffrey M., and Michelle N. Yerman. "Behavior of Larval Butterflyfishes (Teleostei: Chaetodontidae) at Settlement on Coral Reefs." Copeia 2012, no. 2 (2012): 211–21. http://dx.doi.org/10.1643/ce-10-185.

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38

Woods, Christopher, Jacqueline Webb, and Darlene Ketten. "The physoclistous swim bladder of chaetodontid butterflyfishes: Implications for acoustic function." Journal of the Acoustical Society of America 120, no. 5 (2006): 3326. http://dx.doi.org/10.1121/1.4781233.

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39

Berumen, Michael L., and Morgan S. Pratchett. "Trade-offs associated with dietary specialization in corallivorous butterflyfishes (Chaetodontidae: Chaetodon)." Behavioral Ecology and Sociobiology 62, no. 6 (2007): 989–94. http://dx.doi.org/10.1007/s00265-007-0526-8.

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40

Pratchett*†, M. S., S. K. Wilson‡§, and A. H. Baird. "Declines in the abundance of Chaetodon butterflyfishes following extensive coral depletion." Journal of Fish Biology 69, no. 5 (2006): 1269–80. http://dx.doi.org/10.1111/j.1095-8649.2006.01161.x.

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41

Leis, Jeffrey M. "Larval biology of butterflyfishes (Pisces, Chaetodontidae): what do we really know?" Environmental Biology of Fishes 25, no. 1-3 (1989): 87–100. http://dx.doi.org/10.1007/bf00002203.

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42

Tricas, Timothy C. "Prey selection by coral-feeding butterflyfishes: strategies to maximize the profit." Environmental Biology of Fishes 25, no. 1-3 (1989): 171–85. http://dx.doi.org/10.1007/bf00002210.

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43

Findley, James S., and Muriel T. Findley. "GLOBAL, REGIONAL, AND LOCAL PATTERNS IN SPECIES RICHNESS AND ABUNDANCE OF BUTTERFLYFISHES." Ecological Monographs 71, no. 1 (2001): 69–91. http://dx.doi.org/10.1890/0012-9615(2001)071[0069:gralpi]2.0.co;2.

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44

Roberts, Callum M., Alexander R. Dawson Shepherd, and Rupert F. G. Ormond. "Large-Scale Variation in Assemblage Structure of Red Sea Butterflyfishes and Angelfishes." Journal of Biogeography 19, no. 3 (1992): 239. http://dx.doi.org/10.2307/2845449.

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45

Villanueva, R. D., and A. J. Edwards. "Butterflyfishes feed on externally brooded larvae of the blue coral, Heliopora coerulea." Coral Reefs 29, no. 1 (2009): 105. http://dx.doi.org/10.1007/s00338-009-0553-1.

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46

Thompson, Cassandra A., Samuel Matthews, Andrew S. Hoey, and Morgan S. Pratchett. "Changes in sociality of butterflyfishes linked to population declines and coral loss." Coral Reefs 38, no. 3 (2019): 527–37. http://dx.doi.org/10.1007/s00338-019-01792-x.

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47

Ferry-Graham, L. A., P. C. Wainwright, and D. R. Bellwood. "Novel morphologies & prey capture consequence: long vs. short-jawed butterflyfishes (chaetodontidae)." Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology 126 (July 2000): 49. http://dx.doi.org/10.1016/s1095-6433(00)80096-3.

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48

Righton, David. "Modelling the effect of resource renewal on the social dynamics of butterflyfishes." Marine and Freshwater Behaviour and Physiology 31, no. 4 (1998): 215–29. http://dx.doi.org/10.1080/10236249809387074.

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49

Pratchett, M. S., and M. L. Berumen. "Interspecific variation in distributions and diets of coral reef butterflyfishes (Teleostei: Chaetodontidae)." Journal of Fish Biology 73, no. 7 (2008): 1730–47. http://dx.doi.org/10.1111/j.1095-8649.2008.02062.x.

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50

Khalaf, Maroof A., and Mohamed Abdallah. "Community structure of butterflyfishes in the Red Sea and Gulf of Aden." Aquatic Conservation: Marine and Freshwater Ecosystems 15, S1 (2005): S77—S89. http://dx.doi.org/10.1002/aqc.708.

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