Skip to main content

Advertisement

Log in

Puddingwife wrasse: an important trophic link of an isolated oceanic island in Brazil

  • Published:
Environmental Biology of Fishes Aims and scope Submit manuscript

Abstract

Invertivorous fish species such as Halichoeres radiatus feed on benthic active prey and need to spend most of their time foraging. Even though the Labridae family is one of the most speciose in reef environments, the knowledge on feeding habits and behavior of this group continues being a major topic on trophic ecology. The present work aimed to evaluate the feeding behavior, diet, and the substrate selectivity of H. radiatus in the remote Saint Peter and Saint Paul Archipelago (SPSPA), where this is the only species of this trophic group, and adds understanding about the role of this species in this singular system. Individuals of H. radiatus were captured and had their diet analyzed in the laboratory to identify and quantify their food items. Direct observations using scuba diving were also performed to describe the daily foraging frequency. Photoquadrats were taken to estimate the substrate relative cover, as a proxy of resource availability. The diet of H. radiatus in SPSPA was mainly composed of damselfish eggs and crustaceans in addition to gastropods, mollusks, and sponges, which reinforces its generalist feeding habits. Individuals of H. radiatus foraged mainly on substrates composed by epilithic algal matrix, which was the most abundant substrate in the study area, but preferred bare rocks and sediment. The foraging activity was constant throughout the daytime, decreasing at sunset. Our results suggest that H. radiatus has a generalist habit, supporting the idea that it is a versatile species, foraging all day long, and constituting an important link in the trophic chain of the archipelago.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

Data availability

The datasets generated during and analyzed during the current study are available from the corresponding author on reasonable request.

References

  • Amundsen P-A, Gabler H-M, Staldvik FJ (1996) A new approach to graphical analysis of feeding strategy from stomach contents data—modification of the Costello (1990) method. J Fish Biol 48(4):607–614. https://doi.org/10.1111/j.1095-8649.1996.tb01455.x

  • Azevedo G (2009) Atividade alimentar e uso do ha bitat por diferentes fases ontogenéticas de Halichoeres poeyi (Pisces: Labridae) em Arraial do Cabo, Rio de Janeiro. Dissertation, Universidade Federal Fluminense.

  • Barrett NS (1995) Short- and long-term movement patterns of six temperate reef fishes (Families Labridae and Monacanthidae). Mar Freshw Res 46:853–860

    Article  Google Scholar 

  • Bell T, Kramer DL (2000) Territoriality and habitat use by juvenile blue tangs, Acanthurus coeruleus. Environ Biol Fishes 58:401–409

    Article  Google Scholar 

  • Bellwood DR, Wainwright PC (2001) Locomotion in labrid fishes: implications for habitat use and cross-shelf biogeography on the Great Barrier Reef. Coral Reefs 20:139–150. https://doi.org/10.1007/s003380100156

    Article  Google Scholar 

  • Bellwood DR (1996) The Eocene fishes of Monte Bolca: the earliest coral reef fish assemblage. Coral Reefs 15:11–19

    Article  Google Scholar 

  • Bonaldo RM, Krajewski JP, Sazima I (2005) Meals for two: foraging activity of the butterflyfish Chaetodon striatus (Perciformes) in Southeast Brazil. Braz J Biol 65:1–6

    Article  Google Scholar 

  • Bonaldo RM, Bellwood DR (2008) Fish size and functional role on coral reefs. Mar Ecol Prog Ser 360:237–244

    Article  Google Scholar 

  • Carvalho-Filho A (1999) Peixes: Costa Brasileira. 3a edição. Editora Melro, São Paulo

  • Chaves LCT, Monteiro-Neto C (2009) Comparative analysis of rocky reef fish community structure in coastal islands of south-eastern Brazil. J Mar Bio Assoc UK 89(3):609–619

    Article  Google Scholar 

  • Coni EOC, Nunes JACC, Ferreira CM, Maia-Nogueira R, Medeiros DV, Sampaio CLS (2010) The Spanish hogfish Bodianus rufus (Labridae) acting as cleaner of nocturnal fish in the north-east of Brazil. JMBA2 Mar Biodivers Rec 3:e23 https://doi.org/10.1017/S1755267210000187

  • Coni EOC, Nunes JACC, Sampaio CLS (2007) Halichoeres penrosei (Labridae), a sporadic cleaner wrasse. JMBA2 Mar Biodivers Rec 1:e82 https://doi.org/10.1017/S1755267207008494

  • Costello MJ (1990) Predator feeding strategy and prey importance: a new graphical analysis. J Fish Biol 36:261–263

    Article  Google Scholar 

  • Covich AP (1976) Analyzing shapes of foraging areas: some ecological and economic theories. Annu Rev Ecol Syst 7:235–257

    Article  Google Scholar 

  • Cowen RK (1986) Site-specific differences in the feeding ecology of the California sheephead, Semicossyphus pulcher (Labridae). Environ Biol Fish 16:193–203

    Article  Google Scholar 

  • Cowman PF, Bellwood DR, Herwerden LV (2009) Dating the evolutionary origins of wrasse lineages (Labridae) and the rise of trophic novelty on coral reefs. Mol Phylogenet Evol 52:621–631

    Article  CAS  PubMed  Google Scholar 

  • Coyer JA (1995) Use of a rock as an anvil for breaking scallops by the yellowhead wrasse, Halichoeres garnoti (Labridae). Bull Mar Sci 57:548–549

    Google Scholar 

  • Cronk QCB (1997) Islands: stability, diversity, conservation. Biodiv Conserv 6:477–493

    Article  Google Scholar 

  • Crossman DJ, Choat JH, Clements KD (2005) Detritus as food for grazing fishes on coral reefs. Limnol Oceanogr 46:1596–1605

    Article  Google Scholar 

  • Curley BG, Kingsford MJ, Gillanders BM (2002) Spatial and habitat- related patterns of temperate reef fish assemblages: implications for the design of marine protected areas. Mar Freshw Res 53:1197–1210. https://doi.org/10.1071/MF01199

    Article  Google Scholar 

  • Darwin C (1859) The origin of species by means of natural selection, 460 pp. Penguin Classics, Harmondsworth

  • Davies NB, Houston AI (1984) Territory economics. In: Krebs JR, Davies NB (eds) Behavioural ecology. Blackwell Scientific, Oxford, UK

  • Dawson MN (2016) Island and island-like marine environments. Glob Ecol Biogeogr 25(7):831–846

    Article  Google Scholar 

  • DeLoach N, Humann P (1999) Reef fish behavior: Florida. New World Publications Inc., Jacksonville Caribbean, Bahamas, p 359

    Google Scholar 

  • Denny CM, Schiel DR (2001) Feeding ecology of the banded wrasse Notolabrus fucicola (Labridae) in southern New Zealand: prey items, seasonal differences, and ontogenetic variation. N Z J Mar Freshw Res 35:925–933. https://doi.org/10.1080/00288330.2001.9517054

    Article  Google Scholar 

  • Edwards A, Lubbock R (1983) The ecology of Saint Paul's Rocks (Equatorial Atlantic). J Zool 200(1):51–69. https://doi.org/10.1111/j.1469-7998.1983.tb06108.x

  • Eristhee N, Oxenford HA (2001) Home range size and use of space by Bermuda chub Kyphosus sectatrix (L.) in 2 marine reserves in the Soufriere Marine Management Area, St. Lucia, West Indies. J Fish Biol 59(Suppl. A):129–151 https://doi.org/10.1006/jfbi.2001.1754

  • Ferreira CEL, Gonçalves JEA, Coutinho R (2001) Fish community structure and habitat complexity in a tropical rocky shore. Environ Biol Fish 61:353–369

    Article  Google Scholar 

  • Floeter SR, Krohling W, Gasparini JL, Ferreira CEL, Zalmon IL (2007) Reef fish community structure on coastal island of south-eastern Brazil: the influence of exposure and benthic cover. Environ Biol Fish 78:147–160

    Article  Google Scholar 

  • Francini-Filho RB, Moura RL, Sazima I (2000) Cleaning by the wrasse Thalassoma noronhanum, with two records of predation by its grouper client Cephalopholis fulva. J Fish Biol 56:802–809

    Google Scholar 

  • Froese R, Pauly D (eds) (2010) World wide web electronic publication. http://www.fishbase.org (Accessed 23 September 2010)

  • Fulton CJ, Bellwood DR, Wainwright PC (2001) The relationship between swimming ability and habitat use in wrasses (Labridae). Mar Biol 139:25–33

    Article  Google Scholar 

  • Fulton CJ, Bellwood DR (2002) Ontogenetic habitat use in labrid fshes: an ecomorphological perspective. Mar Ecol Prog Ser 236:255–262

    Article  Google Scholar 

  • Fulton CJ, Bellwood DR (2002) Patterns of foraging in labrid fishes. Mar Ecol Prog Ser 226:135–142

    Article  Google Scholar 

  • Fuiman LA, Connelly TL, Lowerre-Barbieri SK, McClelland JW (2015) Egg boons: central components of marine fatty acid food webs. Ecology 96(2):362–372

    Article  PubMed  Google Scholar 

  • Gerking SD (1994) Feeding ecology of fish. Academic Press, California, USA

    Google Scholar 

  • Gillanders BM, Kingsford MJ (1998) Influence of habitat on abundance and size structure of a large temperate-reef fish, Achoerodus viridis (Pisces: Labridae). Mar Biol 132:503–514. https://doi.org/10.1007/S002270050416

    Article  Google Scholar 

  • Gronell A (1980) Space utilization by the cocoa damselfish, Eupomacentrus variabilis (Pisces: Pomacentridae). Bull Mar Sci 30:237–251

    Google Scholar 

  • Grossman GD (1986) Food resource partitioning in a rocky intertidal fish assemblage. J Zool (Lond) 1:317–355

    Article  Google Scholar 

  • Hahn NS, Agostinho AA, Goitein R (1997) Feeding ecology of curvina Plagioscion squamossissimus (Hechel, 1840) (Osteichthyes, Perciformes) in the Itaipu Reservoir and Porto Rico floodplain. Acta Limn Bras 9:11–22

    Google Scholar 

  • Helfman GS, Collette BB, Facey DE (1997) The diversity of fishes. Blackwell Science, Inc., Massachusetts, United States, p 528

    Google Scholar 

  • Hews DK (1993) Food resources affect female distribution and male mating opportunities in the iguanian lizard Uta palmeri. Anim Behav 46:279–291

    Article  Google Scholar 

  • Hobbs JP, Jones GP, Munday PL, Connoly SR, Srinivasan M (2012) Biogeography and the structure of coral reef fish communities on isolated islands. J Biogeog 39(1):130–13

    Article  Google Scholar 

  • Hobson ES (1974) Feeding patterns among tropical fishes. Am Sci 63:382–392

    Google Scholar 

  • Hobson ES (1974) Feeding relationships of teleostean fishes on coral reefs in Kona, Hawaii. Fish Bull (Wash DC) 72(915–103):1

    Google Scholar 

  • Hobson ES (1975) Feeding patterns among tropical reef fishes. Am Sci 63:382–392

    Google Scholar 

  • Hooker JD (1847) On the vegetation of the Galapagos Archipelago as compared with that of some other tropical islands and of the continent of America. Trans Linnean Soc Lond 20:235–262

    Article  Google Scholar 

  • Humann P, Deloach N (2002) Reef fish identification, 3rd edn. New World Publication, Florida, p 481p

    Google Scholar 

  • Hyslop EJ (1980) Stomach content analysis: a review of methods and their application. J Fish Biol 17:411–429

    Article  Google Scholar 

  • Itzkowitz M (1979) The feeding strategies of a facultative cleanerfish, Thalassoma bifasciatum (Pisces: Labridae). J Zool (Lond) 187:403–413

    Article  Google Scholar 

  • Ivlev VS (1961) Experimental ecology of the feeding of fishes. Yale University Press, New Haven, Connecticut, USA

    Google Scholar 

  • Jones GP (1984) Population ecology of the temperate reef fish Pseudolabrus celidotus Bloch & Schneider (Pisces: Labridae). I. Factors influencing recruitment. J Exp Mar Biol Ecol 75:257–276. https://doi.org/10.1016/0022-0981(84)90170-9

    Article  Google Scholar 

  • Jones GP, Syms G (1998) Disturbance, habitat structure and the ecology of reef fish on coral reefs. Aust J Ecol 23:287–297

    Article  Google Scholar 

  • Jones KMM (2002) Behavioural overlap in six Caribbean labrid species: intra- and interspecific similarities. Environ Biol Fish 65:71–81

    Article  Google Scholar 

  • Jones KMM (2005) Home range areas and activity centres in six species of Caribbean wrasses (Family Labridae). J Fish Biol 66:150–166

    Article  Google Scholar 

  • Jones KMM (2006) Distribution of behaviours and species interactions within home range areas contours in five Caribbean reef fish species (Family Labridae). Environ Biol Fish 80(1):35–49. https://doi.org/10.1007/s10641-006-9104-6

    Article  Google Scholar 

  • Jones KMM (2002) Behavioural overlap in six Caribbean labrid species: intra- and interspecific similarities. Environ Biol Fishes 65:71–81

    Article  Google Scholar 

  • Jones KMM (2007) Distribution of behaviours and species interactions within home range contours in five Caribbean reef fish species (Family Labridae). Environ Biol Fishes 80:35–49. https://doi.org/10.1007/s10641-006-9104-6

    Article  Google Scholar 

  • Kawakami E, Vazzoler G (1980) Método gráfico e estimativa de índice alimentar aplicado no estudo de alimentação de peixes. Bol Inst Oceanogr 29:205–207

    Article  Google Scholar 

  • Keenleyside MHA (1972) The behaviour of Abudefduf zonatus (Pisces, Pomacentridae) at Heron Island, Great Barrier Reef. Anim Behav 20:763–774

    Article  Google Scholar 

  • Kohler KE, Gill SM (2006) Coral Point Count with Excel extensions (CPCe): a Visual Basic program for the determination of coral and substrate coverage using random point count methodology. Comput Geosci 32(9):1259–1269

    Article  Google Scholar 

  • Krajewski JP, Bonaldo RM, Sazima C, Sazima I (2006) Foraging activity and behaviour of two goatfish species (Perciformes: Mullidae) at Fernando de Noronha Archipelago, tropical West Atlantic. Environ Biol Fishes 77:1–8

    Article  Google Scholar 

  • Krajewski JP, Floeter SR, Jones G, Leite F (2010) Patterns of variation in behavior within and among reef fish species on an isolated tropical island: influence of exposure and substratum. J Mar Biol Assoc UK 91(6):1359–1368. https://doi.org/10.1017/S0025315410000111

    Article  Google Scholar 

  • Krajewski JP, Floeter SR (2011) Reef fish community structure of the Fernando de Noronha Archipelago (Equatorial Western Atlantic): the influence of exposure and benthic composition. Environ Biol Fishes 92:25–40. https://doi.org/10.1007/s10641-011-9813-3

    Article  Google Scholar 

  • Kramer MJ, Bellwood O, Bellwood DR (2016) Foraging and microhabitat use by crustacean-feeding wrasses on coral reefs. Mar Ecol Prog Ser 548:277–282

    Article  Google Scholar 

  • Krebs CJ (1989) Ecological methodology. Harper Collin Publishers, New York

    Google Scholar 

  • Lehner PN (1998) Handbook of ethological methods. Cambridge University Press, Cambridge

    Google Scholar 

  • Liem KF, Sanderson SL (1986) The pharyngeal jaw apparatus of labrid fishes: a functional morphological perspective. J Morphol 187:143–158

    Article  PubMed  Google Scholar 

  • Low RM (1971) Interspecific territoriality in a pomacentrid reef fish, Pomacentrus flavicauda Whitley. Ecology 52:649–654

    Article  Google Scholar 

  • Luckhurst BE, Luckhurst K (1978) Diurnal space utilization in coral reef fish communities. Mar Biol 49:325–332

    Article  Google Scholar 

  • Luiz OJ, Mendes TC, Barneche DR, Ferreira CGW, Noguchi R, Villaça RC, … Ferreira CEL (2015) Community structure of reef fishes on a remote oceanic island (St Peter and St Paul’s Archipelago, equatorial Atlantic): the relative influence of abiotic and biotic variables. Mar Freshw Res 66(8):739–749https://doi.org/10.1071/MF14150

  • MacAarthur RH, Pianka ER (1966) On optimal use of a patchy environment. Am Nat 100(916):603–609

    Article  Google Scholar 

  • Manly BFJ, Thomas DL, Mcdonald TL (2002) Resource selection by animals: statistical design an analisys for field studies, 2nd edn. Springer-Verlag, New York, LLC, p 240

    Google Scholar 

  • McArthur RH, Wilson EO (1967) The theory of island biogeography. Princeton University Press, US, p 203

    Google Scholar 

  • Meyer CG, Holland KN, Wetherbee BM, Lowe CG (2000) Movement patterns, habitat utilization, home range size and site fidelity of whitesaddle goat fish, Parupeneus porphyreus, in a marine reserve. Enviro Biol Fishes 59:235–242

    Article  Google Scholar 

  • Morton JK, Platell ME, Gladstone W (2008) Differences in feeding ecology among three co-occurring species of wrasse (Teleostei: Labridae) on rocky reefs of temperate Australia. Mar Biol 154:577–592. https://doi.org/10.1007/S00227-008-0951-X

    Article  Google Scholar 

  • Mumby PJ, Wabnitz CCC (2002) Spatial patterns of aggression, territory size, and harem size in five sympatric Caribbean parrotfish species. Environ Biol Fishes 63:265–279

    Article  Google Scholar 

  • Nemtzov SC (1997) Intraspecific variation in home range exclusivity by female green razorfish, Xyrichtys splendens (family Labridae), in different habitats. Environ Biol Fishes 50:371–381

    Article  Google Scholar 

  • Norberg RA (1977) An ecological theory on foraging time and energetics and choice of optimal food searching method. J Anim Ecol 46:511

    Article  Google Scholar 

  • Norman MD, Jones GP (1984) Determinants of territory size in the pomacentrid reef fish, Parma victoriae. Oecologia 61:60–69

    Article  CAS  PubMed  Google Scholar 

  • Nunes JdACC, Sampaio CLS, Barros F (2013) How wave exposure, group size and habitat complexity influence foraging and population densities in fishes of the genus Halichoeres (Perciformes: Labridae) on tropical rocky shores. Mar Biol 160(9):2383–94

    Article  Google Scholar 

  • Nursall JR (1977) Territoriality in the red lip blennies (Ophioblennius atlanticus – Pisces: Blenniidae). J Zool, London 182:205–223

    Article  Google Scholar 

  • Oliveira AK, Alvim MCC, Peret AC, Alves CBM (2004) Diet shifts related to body size of the pirambeba Serrasalmus brandtii Lütken, 1875 (Osteichthyes, Serrasalminae) in the Cajuru Reservoir, São Francisco River basin, Brazil. Braz J Biol 64:117–124

    Article  CAS  PubMed  Google Scholar 

  • Luiz OJ, Madin JSD, Robertson R, Rocha LA, Wirtz P, Floeter SR (2012) Ecological traits influencing range expansion across large oceanic dispersal barriers: insights from tropical Atlantic reef fishes. Proc R Soc B 279:1033–1040. https://doi.org/10.1098/rspb.2011.1525

    Article  PubMed  Google Scholar 

  • Parenti P, Randall JE (2000) An annotated checklist of the species of the Labroid Wsh families Labridae and Scaridae. Ichth Bull 68:1–97

    Google Scholar 

  • Preskitt LB, Vroom PS, Smith CM (2004) A rapid ecological assessment (REA) quantitative survey method for benthic algae using photoquadrats with scuba. Pac Sci 58:201–209

    Article  Google Scholar 

  • Randall JE (1967) Food habits of reef fishes of the West Indies. Stud Trop Oceanogr 5:665–847

    Google Scholar 

  • Reinboth R (1973) Dualistic reproductive behavior in the protogynous wrasse, Thalassoma bifasciatum and some observations on its day-night changeover. Helgolander Meeresun 24:174–191

    Article  Google Scholar 

  • Robertson DR (1981) The social and mating systems of two labrid fishes, Halichoeres maculipinna and H. garnoti, off the Caribbean Coast of Panama. Mar Biol 64:327–340

    Article  Google Scholar 

  • Rocha LA, Pinheiro TH, Gasparini JL (2010) Description of Halichoeres rubrovirens, a new species of wrasse (Labridae: Perciformes) from the Trindade and Martin Vaz Island group, southeastern Brazil, with a preliminary mtDNA molecular phylogeny of New World Halichoeres. Zootaxa 2422:22–30

    Article  Google Scholar 

  • Vitousek PM (1988) Diversity and biological invasions of oceanic islands. In: Biodiversity, Wilson EO (ed). National Academy Press. Washington, D.C. 538pp

  • Roede MJ (1972) Color as related to size, sex, and behavior in seven Caribbean Labrid Fish Species (Genera Thalassoma, Halichoeres, Hemipteronotus). Stud Fauna Curacao Other Caribb Isl 138:1–264

    Google Scholar 

  • Sale PF (1971) Extremely limited home range in a coral reef fish, Dascyllus aruanus (Pisces: Pomacentridae). Copeia 1971:324–327

    Article  Google Scholar 

  • Samoilys MA (1997) Movement in a large predatory fish: coral trout, Plectropomus leopardus (Pisces: Serranidae), on Heron Reef, Australia. Coral Reefs 16:151–158

    Article  Google Scholar 

  • Samoylis MA, Carlos G (2000) Determining methods of underwater visual census for estimating the abundance of coral reef fishes. Environ Biol Fish 57:289–304

    Article  Google Scholar 

  • Sazima C, Bonaldo RM, Krajewski JP, Sazima I (2005) The Noronha wrasse: a “jack-of-all-trades” follower. Aqua 9:97–108

    Google Scholar 

  • Sazima I, Krajewski JP, Bonaldo RM, Sazima C (2005) Wolf in a sheep’s clothes: juvenile coney (Cephalopholis fulva) as an aggressive mimic of the brown chromis (Chromis multilineata). Neotrop Ichthyol 3:315–318

    Article  Google Scholar 

  • Sazima I, Moura RL, Gasparini JL (1998) The wrasse Halichoeres cyanocephalus (Labridae) as a specialized cleaner fish. Bull Mar Sci 63:605–610

    Google Scholar 

  • Schoener TW (1971) Theory of feeding strategies. Annu Ver Ecol Syst 11:369–404

    Article  Google Scholar 

  • Shapiro DY, Garcia-Moliner G, Sadovy Y (1994) Social system of an inshore stock of the red hind grouper, Epinephelus guttatus (Pisces: Serranidae). Environ Biol Fishes 41:415–422

    Article  Google Scholar 

  • Shepherd SA, Clarkson PS (2001) Diet, feeding behaviour, activity and predation of the temperate blue-throated wrasse, Notolabrus tetricus. Mar Freshw Res 52:311–322. https://doi.org/10.1071/MF99040

    Article  Google Scholar 

  • Stamps JA, Buechner M, Krishnan VV (1987) The effects of habitat geometry on territorial defense costs: intruder pressure in bounded habitats. Am Zool 27:307–325

    Article  Google Scholar 

  • Thresher RE (1979) Social behavior and ecology of two sympatric wrasses (Labridae: Halichoeres spp.) off the coast of Florida. Mar Biol 53:161–172

    Article  Google Scholar 

  • Underwood AJ (1997) Experiments in ecology: their logical design and interpretation using analysis of variance. Cambridge Univ. Press, Cambridge

    Google Scholar 

  • van Rooij JM, Kroon FJ, Videler JJ (1996) The social and mating system of the herbivorous reef fish Sparisoma viride: one-male versus multi-male groups. Environ Biol Fishes 47:353–378

    Article  Google Scholar 

  • Wainwright PC, Bellwood DR, Westneat MW, Grubrich JR, Hoey AS (2004) A functional morphospace for the skull of labrid fishes: patterns of diversity in a complex biomechanical system. Biol J Linn Soc 82:1–25

    Article  Google Scholar 

  • Wainwright PC (1987) Biomechanical limits to ecological performance: mollusc crushing by the Caribbean Hogfish, Lachnolaimus maximus (Labridae). J Zool, London 213:283–297

    Article  Google Scholar 

  • Wainwright PC (1988) Morphology and ecology: functional basis of feeding constraints in Caribbean labrid fishes. Ecology 69(3):635–645

    Article  Google Scholar 

  • Walter HS (2004) The mismeasure of islands: implications for biogeographical theory and the conservation of nature. J Biogeogr 31(2):177–197

    Article  Google Scholar 

  • Warner RR, Robertson DR (1978) Sexual patterns in the labroid fishes of the Western Caribbean, I: The wrasses (Labridae). Smithson Contrib Zool 254:1–27

    Article  Google Scholar 

  • Whittaker RJ, Fernández-Palacios JM, Matthews TJ, Borregaard MK, Triantis KA (2017) Island biogeography: taking the long view of nature’s laboratories. Science 357:885

    Article  CAS  Google Scholar 

  • Whittaker RJ, Triantis KA, Ladle RJ (2010) A general dynamic theory of oceanic Island Biogeography: extending the MacArthur-Wilson theory to accommodate the rise and fall of volcanic islands. In: Losos JB, Ricklefs RE. The theory of Island Biogeography revisited. Princeton University Press, USA. 476pp.

  • Wilson SK, Belwood DR, Choat JH, Furnas MJ (2003) Detritus in the epilithic algal matrix and its use by coral reef fishes. Oceanogr Mar Biol Annu Rev 41:279–309

    Google Scholar 

  • Yamaoka K (1978) Pharyngealjaw structure in labrid fishes. Publ Seto Mar Biol Lab 24:409–426

    Article  Google Scholar 

  • Zar JH (1999) Biostatistical analysis, 4th edn. Prentice Hall, Upper Saddle River, New Jersey

    Google Scholar 

  • Zeller DC (1997) Home range and activity patterns of the coral trout Plectropomus leopardus (Serranidae). Mar Ecol Prog Ser 154:65–77

    Article  Google Scholar 

Download references

Acknowledgements

We thank M Sissini and H Burnier for language review of the manuscript, A Dalben and Olga for field assistance, besides V Giglio and other reviewers for helpful comments.

Funding

This work was supported by the Conselho Nacional de Desenvolvimento Científico e Tecnológico — CNPQ (Programa Pro-Arquipélago) and Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro — FAPERJ (MBL scholarship). CAMMC is also grateful to FAPERJ for the post-doctoral scholarship (grant E-26/202.310/2019).

Author information

Authors and Affiliations

Authors

Contributions

All authors have read, revised, and approved the submitted version of the manuscript.

Corresponding author

Correspondence to Cesar A. M. M. Cordeiro.

Ethics declarations

Ethical approval

All sampling have been conducted as per the guidelines of the federal environmental authority (Instituto Chico Mendes de Conservação da Biodiversidade — ICMBio) which provided the proper permit and consent (ICMBio permit #25678-1) before sampling activities. No approval of research ethics committees was required to accomplish the goals of this study because it was considered as a fishing activity by competent authorities. However, all animals involved were captured following strict practices causing instant death to avoid and minimize animal suffering.

Competing interests

The authors declare no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Appendix

Appendix

Table

Table 2 Substrate availability (%) at St Peter and St Paul Archipelago, percentage bites per substrate invested by Halichoeres radiatus

2

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

de Lucena, M.B., Cordeiro, C.A.M.M., Valentin, J.L. et al. Puddingwife wrasse: an important trophic link of an isolated oceanic island in Brazil. Environ Biol Fish 105, 561–573 (2022). https://doi.org/10.1007/s10641-022-01265-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10641-022-01265-1

Keywords

Navigation