Hostname: page-component-669899f699-rg895 Total loading time: 0 Render date: 2025-05-01T18:16:57.416Z Has data issue: false hasContentIssue false

Morphological variation of the endemic reef-building genus Mussismilia in the Bahia State (Tropical northeastern Brazilian coast)

Published online by Cambridge University Press:  13 December 2024

A. H. Silva*
Affiliation:
LABIMAR (Laboratório de Invertebrados Marinhos: Crustacea, Cnidaria e Fauna Associada), Instituto de Biologia, Universidade Federal da Bahia (UFBA), Rua Barão de Jeremoabo, 147, Ondina, Salvador, BA CEP 40170115, Brazil
M. M. Nogueira
Affiliation:
LABIMAR (Laboratório de Invertebrados Marinhos: Crustacea, Cnidaria e Fauna Associada), Instituto de Biologia, Universidade Federal da Bahia (UFBA), Rua Barão de Jeremoabo, 147, Ondina, Salvador, BA CEP 40170115, Brazil
R. Johnsson
Affiliation:
LABIMAR (Laboratório de Invertebrados Marinhos: Crustacea, Cnidaria e Fauna Associada), Instituto de Biologia, Universidade Federal da Bahia (UFBA), Rua Barão de Jeremoabo, 147, Ondina, Salvador, BA CEP 40170115, Brazil
E. G. Neves
Affiliation:
LABIMAR (Laboratório de Invertebrados Marinhos: Crustacea, Cnidaria e Fauna Associada), Instituto de Biologia, Universidade Federal da Bahia (UFBA), Rua Barão de Jeremoabo, 147, Ondina, Salvador, BA CEP 40170115, Brazil
*
Corresponding author: A. H. Silva; Email: [email protected]

Abstract

Verrill's modern Mussismilia (the ‘brain corals’) were described in the 19th century, being hitherto considered endemic reef-building species to Brazil. Contrasting with the original diagnoses, highly variable morphological patterns have been observed among the congeners. Interspecific overlapping of major taxonomical characters has resulted in quite inconclusive use of the skeleton macromorphology for the genus. Intending to corroborate the Mussismilia taxonomy, a comparative morphological approach was developed, combining skeleton macro- and micromorphology. A total of 132 colonies was collected between 13°S and 17°S latitude (Mussismilia hispida = 53, Mussismilia harttii = 41, and Mussismilia braziliensis = 38). Qualitative (n = 9) and quantitative characters (n = 7) were selected (the latter was analysed with Kruskal–Wallis and a principal component analysis). A non-parametric test was adopted due to heteroscedasticity and the irregular sampling among populations. As a result, the corallite diameter and number of septa were significantly distinct among the species (α = 0.05). Micromorphology also differs interspecifically, being distribution and size of septal spines diagnostic for the congeners. Intraspecific variation and morphs are approached, ensuring the relevance of the skeleton for the interspecific delimitation and the species identities. Finally, field identification and/or methods based on image analyses from video transects should be adopted with caution. These practices may provide unreliable data, once the information is restricted to the view of the colony top, resulting in biased identification – majorly if the morphotypes of M. harttii and M. hispida share closely spaced corallites.

Type
Research Article
Copyright
Copyright © The Author(s), 2024. Published by Cambridge University Press on behalf of Marine Biological Association of the United Kingdom

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Article purchase

Temporarily unavailable

References

Amaral, FD (1992) Sobre Favia leptophylla Verrill, 1868 (Cnidaria, Sclaractinia). Iheringia Série Zoológica 73, 117118.Google Scholar
Amaral, FMS (1994) Morphological variation in the reef coral Montastrea cavernosa in Brazil. Coral Reefs 13, 113117.CrossRefGoogle Scholar
Amaral, FMS and Ramos, CAC (2007) Skeletal variability of the coral Favia gravida (Verrill, 1868) from Brazil. Biota Neotropica 7, 245251.CrossRefGoogle Scholar
Amaral, FMS, Ramos, CAC, Leão, ZMAN, Kikuchi, RKP, Lima, KKM, Longo, LL, Cordeiro, RTS, Lira, SMA and Vasconcelos, SL (2009) Checklist and morphometry of benthic cnidarians from the Fernando de Noronha Archipelago, Brazil. Cahiers de Biologie Marine 50, 277290.Google Scholar
Arrigoni, R, Stefani, F, Pichon, M, Galli, P and Benzoni, F (2012) Molecular phylogeny of the Robust clade (Faviidae, Mussidae, Merulinidae, and Pectiniidae): an Indian Ocean perspective. Molecular Phylogenetics and Evolution 65, 184193.CrossRefGoogle ScholarPubMed
Benzoni, F, Arrigoni, R, Stefani, F and Pichon, M (2011) Phylogeny of the coral genus Plesiastrea (Cnidaria, Scleractinia). Contributions to Zoology 80, 231249.CrossRefGoogle Scholar
Brown, D and Navin, KF (1992) An interactive knowledge base for the identification of scleractinian corals. Proceedings of the 7th International Coral Reefs Symposium 2, 661664.Google Scholar
Bruno, JF and Edmunds, PJ (1997) Clonal variation for phenotypic plasticity in the coral Madracis mirabilis. Ecology 78, 21772190.CrossRefGoogle Scholar
Budd, AF, Fukami, H, Smith, ND and Knowlton, N (2012a) Taxonomic classification of the reef coral family Mussidae (Cnidaria: Anthozoa: Scleractinia). Zoological Journal of the Linnean Society 166, 465529.CrossRefGoogle Scholar
Budd, AF, Romano, SL, Smith, ND and Barbeitos, MS (2012b) Rethinking the phylogeny of scleractinian corals: a review of morphological and molecular data. Integrative and Comparative Biology 3, 411427.Google Scholar
Budd, AF and Stolarski, J (2009) Searching for new morphological characters in the systematics of scleractinian reef corals: comparison of septal teeth and granules between Atlantic and Pacific Mussidae. Acta Zoologica 90, 142165.CrossRefGoogle Scholar
Castro, CB and Pires, DO (2001) Brazilian coral reefs: what we already know and what is still missing. Bulletin of Marine Science 69, 357371.Google Scholar
Dutra, LXC, Kikuchi, RKP and Leão, ZMAN (2006) Effects of sediment accumulation on reef corals from Abrolhos, Bahia, Brazil. Journal of Coastal Research 39, 633638.Google Scholar
Foster, AB (1977) Patterns of small-scale variation of skeletal morphology within the scleractinian corals, Montastraea annularis and Siderastrea siderea. Proceedings of the 3rd International Coral Reefs Symposium 2, 409415.Google Scholar
Foster, AB (1979) Phenotypic plasticity in the reef corals Montastrea annularis (Ellis & Solander) and Siderastrea siderea (Ellis & Solander). Journal of Experimental Marine Biology and Ecology 39, 2554.CrossRefGoogle Scholar
Foster, AB (1985) Variation within coral colonies and its importance for interpreting fossil species. Journal of Paleontology 59, 13591381.Google Scholar
Francini-Filho, RB, Moura, RL, Thompson, FL, Reis, RM, Kaufman, L, Kikuchi, RKP and Leão, ZMAN (2008) Diseases leading to accelerated decline of reef corals in the largest South Atlantic reef complex (Abrolhos Bank, eastern Brazil). Marine Pollution Bulletin 56, 10081014.CrossRefGoogle ScholarPubMed
Fukami, H, Budd, AF, Paulay, G, Solé-Cava, A, Chen, CA, Iwao, K and Knowlton, N (2004) Conventional taxonomy obscures deep divergence between Pacific and Atlantic corals. Nature 427, 832835.CrossRefGoogle ScholarPubMed
Fukami, H, Chen, CA, Budd, AF, Collins, A, Wallace, C, Chuang, Y-Y, Chen, C, Dai, C-F, Iwao, K, Sheppard, C, Knowlton, N and Ahmed, N (2008) Mitochondrial and nuclear genes suggest that stony corals are monophyletic but most families of stony corals are not (order Scleractinia, class Anthozoa, phylum Cnidaria). PLoS ONE 3(9), e2222.CrossRefGoogle Scholar
Jolliffe, IT (2002) Principal Component Analysis. Springer Series in Statistic, 2nd Edn. New York: Springer.Google Scholar
Kubicek, A, Breckling, B, Hoegh-Guldberg, O and Reuter, H (2019) Climate change drives trait-shifts in coral reef communities. Scientific Reports 9, 3721.CrossRefGoogle ScholarPubMed
Laborel, J (1969/70) Madreporaires et hidrocoralliaires récifaux dês cotes brésiliennes: systematique, écologie, réparttion verticale et géographique. Campagne de la Calypso au large dês cotes atlantiques de I'Amerique do Sud. Annales de l'Institut Océanographique 47, 15229.Google Scholar
Leão, ZMAN, Kikuchi, RKP, Ferreira, BP, Neves, EG, Sovierzoski, HH, Oliveira, MDM, Maida, M, Correia, MD and Jonhsson, R (2016) Brazilian coral reefs in a period of global changes: a synthesis. Brazilian Journal of Oceanography 64, 97116.CrossRefGoogle Scholar
Maida, M and Ferreira, BP (1997) Coral reefs of Brazil: an overview. Proceedings of the 8th International Coral Reefs Symposium 1, 263274.Google Scholar
Menezes, NM, Neves, EG, Barros, F, Kikuchi, RKP and Johnsson, R (2013) Intracolonial variation in Siderastrea de Blainville, 1830 (Anthozoa, Scleractinia): taxonomy under challenging morphological constraints. Biota Neotropica 13, 108116.CrossRefGoogle Scholar
Miranda, RJ, Cruz, ICS and Leão, ZMAN (2013) Coral bleaching in the Caramuanas reef (Todos os Santos Bay, Brazil) during the 2010 El Niño event. Latin American Journal of Aquatic Research 41, 351360.CrossRefGoogle Scholar
Neves, EG (2004) Complexo Siderastrea: espécies distintas? Significado da variabilidade do gênero Siderastrea de Blainville, 1830 (Anthozoa: Scleractinia) no Brasil (PhD thesis). Univerdidade de São Paulo, São Paulo, Brazil.Google Scholar
Neves, EG, Andrade, SCS, Lang, FS and Solferini, VN (2008) Genetic variation and population structuring in two brooding coral species (Siderastrea stellata and Siderastrea radians) from Brazil. Genetica 132, 243254.CrossRefGoogle ScholarPubMed
Neves, EG, Johnsson, R, Sampaio, C and Pichon, M (2006) The occurrence of Scolymia cubensis in Brazil: revising the problem of the Caribbean solitary mussids. Zootaxa 1366, 4554.CrossRefGoogle Scholar
Nogueira, MM, Neves, E and Johnsson, R (2015) Effects of habitat structure on the epifaunal community in Mussismilia corals: does coral morphology influence the richness and abundance of associated crustacean fauna? Helgoland Marine Research 69, 221229.CrossRefGoogle Scholar
Nunes, F, Fukami, H, Vollmer, SV, Norris, RD and Knowlton, N (2008) Re-evaluation of the systematics of the endemic corals of Brazil by molecular data. Coral Reefs 27, 423432.CrossRefGoogle Scholar
Oksanen, J, Blanchet, FG, Friendly, M, Kindt, R, Legendre, P, Mcglinn, D, Minchin, PR, O'hara, RB, Simpson, GL, Solymos, P, Stevens, MHH, Szoecs, E and Wagner, H (2017) Vegan: Community Ecology Package. R package version 2.4-0. Available at https://CRAN.R-project.org/package=veganGoogle Scholar
Riegl, B and Piller, WE (2000) Reefs and coral carpets in the Miocene Paratethys (Badenian, Leitha Limestone, Austria). Proceedings of the 9th International Coral Reefs Symposium 1, 211216.Google Scholar
Romano, SL and Cairns, SD (2000) Molecular phylogenetic hypotheses for the evolution of scleractinian corals. Bulletin of Marine Science 67, 10431068.Google Scholar
Santos, MG, Amaral, FD, Hernández, MIM, Knowlton, N and Jara, J (2004) Variação morfológica de Favia gravida Verrill, 1868 e Siderastrea stellata Verrill, 1868 (Cnidaria, Scleractinia): aspectos esqueléticos. Boletim do Museu Nacional Zoologia 517, 19.Google Scholar
Tessler, MG and Goya, SC (2005) Conditioning factors of coastal processes in the Brazilian coastal area. Revista do Departamento de Geografia 17, 1123.Google Scholar
Theodorsson-Norheim, E (1986) Kruskal–Wallis test: basic computer program to perform nonparametric one-way analysis of variance and multiple comparisons on ranks of several independent samples. Computer Methods and Programs in Biomedicine 23, 5762.CrossRefGoogle ScholarPubMed
Veron, JEN (1995) Corals in Space and Time: The Biogeography and Evolution of the Scleractinia, 1st Edn. Sydney: UNSW Press.Google Scholar
Veron, JEN (2000) Corals of the World. Townsville: Sea Challengers, Australian Institute of Marine Science.Google Scholar
Verrill, AE (1868) Notes on Radiata in the Museum of Yale College, with descriptions of new genera and species. No. 4 Notice of the corals and Echinoderms collected by Prof. C.F. Hartt, at the Abrolhos reefs, Province of Bahia, Brazil, 1867. Transactions of the Connecticut Academy of Arts and Sciences 1, 351613.Google Scholar
Verrill, AE (1901) Variations and nomenclature of Bermudas, West Indian and Brazilian reef corals, with notes on various Indo-Pacific corals. Transactions of the Connecticut Academy of Arts and Sciences 11, 128.Google Scholar
Verrill, AE (1902) Comparisons of the Bermudian, West Indian and Brazilian coral faune. Transactions of the Connecticut Academy of Arts and Sciences 11, 169206.Google Scholar
Wickham, H (2009) Ggplot2 Elegant Graphics for Data Analysis, 2nd Edn. New York: Springer.CrossRefGoogle Scholar