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ReefSYN | Standardized datasets of Brazilian reef diversity in space and time - Dataset I: Fish communities from the Brazilian province

Citation

Morais R, Ferreira C E L, Floeter S R, Quimbayo J P, Mendes T C, Longo G O, Cordeiro C A M M, Luza A L (2024). ReefSYN | Standardized datasets of Brazilian reef diversity in space and time - Dataset I: Fish communities from the Brazilian province. Version 3.3. Tropical and Subtropical Western South Atlantic OBIS. Sampling event dataset https://doi.org/10.25607/7nxv5v accessed via GBIF.org on 2025-05-22.

Description

This dataset is part of a broader compilation named 'Standardized datasets of Brazilian reef diversity in space and time' created from a research network of reef scientists within several projects and collaborations and finally gathered and published by the ReefSYN group. This dataset, an updated, filtered and curated version of the one used by Morais et al. (2017), includes fish counts and size estimates in 4,570 transects distributed over 137 localities in 20 different locations, spanning from 0° to 27°S (including oceanic islands). This dataset is the foundation of a large network of reef scientists in Brazil, which started as the project SISBIOTAMar and derived into the PELD ILOC and ReefSYN networks.

Sampling Description

Study Extent

Sampling ranged from the Brazilian northernmost continental shelf reefs of Parcel de Manuel Luís at 0∘ 52′ S; 44∘ 15′ W to the southernmost coastal rocky reefs of Santa Catarina’s coastal islands at 27∘ 50′ S; 48∘ 26′ W. This also included the four oceanic island groups (Saint Paul’s Rocks, 0∘ 54′ N; 29∘ 20′ W; Rocas Atoll, 3∘ 52′ S; 33∘ 48′ W; Fernando de Noronha Archipelago, 3∘ 51′ S; 32∘ 25′ W; and Trindade and Martin Vaz Island group, 20∘ 29′ S; 29∘ 19′ W). In total, over 137 sites in 20 localities were sampled.

Sampling

Fish assemblages along the Brazilian biogeographic province were counted in 4570 transects (20 × 2 m belt transects, underwater visual census - UVC). Samples were obtained in the austral summer from 2001 to 2015. Strip transects performed by snorkeling or scuba diving, during which the diver unwound a tape while identifying, tallying and visually estimating the total length (TL, cm) of non-cryptic fishes >10 cm. While retracting the tape, the diver followed the same procedure for benthic-associated non-cryptic fishes <10 cm and cryptic species (see Morais et al. 2017 for more details). Morais, R.A., Ferreira, C.E.L. & Floeter, S.R. 2017. Spatial patterns of fish standing biomass across Brazilian reefs, Southwestern Atlantic. Journal of Fish Biology, 91: 1642–1667.

Quality Control

The name of all taxa was checked against the WoRMS database (World Register of Marine Species (WoRMS, 2022)), using the R package “worrms” (Chamberlain 2020). Thus, valid scientific names were called “scientificNameAccepted” following the DCS standard. The last checking was done on 23 October 2023, using the version 0.4.2 of ‘worrms’ R package. Some taxonomic updates were made by hand (Hypanus berthalutzae (previously Dasyatis americana), Bathytoshia centroura (Dasyatis centroura), Azurina multilineata (Chromis multilineata), Caranx bartholomaei (Carangoides bartholomaei), Choranthias salmopunctatus (Antias salmopunctatus), Goblioclinus kalisherae (Labrisomus kalisherae), Sphoeroides camila (Sphoeroides spengleri), Serranus flaviventris (Serranus atricauda). We decided to include Menephorus (hybrid between Cephalopholis fulva and Paranthias furcifer) in the dataset so that the record is maintained even with future taxonomic updates of this organism. Also, Scaridae was considered as part of the Labridae family.

Method steps

  1. The number of transects varied considerably among sites (i.e. from five to 242, mean± s.d.=33·4±34·0). To avoid overrepresentation of highly sampled sites, the mean biomass values from all transects of a site were used as the independent observations. The median total fish biomass of coastal localities was used as a reference value with which to contrast individual site values.

Taxonomic Coverages

  1. Ablennes hians
  2. Abudefduf saxatilis
  3. Acanthistius brasilianus
  4. Acanthostracion
  5. Acanthostracion polygonium
  6. Acanthostracion quadricornis
  7. Acanthurus bahianus
  8. Acanthurus chirurgus
  9. Acanthurus coeruleus
  10. Acanthurus monroviae
  11. Aetobatus narinari
  12. Albula vulpes
  13. Alectis ciliaris
  14. Alphestes afer
  15. Aluterus monoceros
  16. Aluterus scriptus
  17. Amblycirrhitus pinos
  18. Amphichthys cryptocentrus
  19. Anisotremus moricandi
  20. Anisotremus surinamensis
  21. Anisotremus virginicus
  22. Antennarius multiocellatus
  23. Apogon
  24. Apogon americanus
  25. Apogon pseudomaculatus
  26. Archosargus rhomboidalis
  27. Aulostomus maculatus
  28. Aulostomus strigosus
  29. Azurina multilineata
  30. Balistes vetula
  31. Bathygobius soporator
  32. Belone belone
  33. Bodianus insularis
  34. Bodianus pulchellus
  35. Bodianus rufus
  36. Bothus lunatus
  37. Bothus ocellatus
  38. Calamus calamus
  39. Calamus penna
  40. Callionymus bairdi
  41. Cantherhines pullus
  42. Canthidermis maculata
  43. Canthidermis sufflamen
  44. Canthigaster figueiredoi
  45. Caranx bartholomaei
  46. Caranx crysos
  47. Caranx hippos
  48. Caranx latus
  49. Caranx lugubris
  50. Caranx ruber
  51. Carcharhinus perezii
  52. Centropomus undecimalis
  53. Centropyge aurantonotus
  54. Cephalopholis fulva
  55. Chaetodipterus faber
  56. Chaetodon ocellatus
  57. Chaetodon sedentarius
  58. Chaetodon striatus
  59. Chilomycterus reticulatus
  60. Chilomycterus spinosus
  61. Chloroscombrus chrysurus
  62. Choranthias salmopunctatus
  63. Chromis flavicauda
  64. Chromis jubauna
  65. Chromis limbata
  66. Chromis scotti
  67. Clepticus brasiliensis
  68. Coryphopterus
  69. Coryphopterus dicrus
  70. Coryphopterus glaucofraenum
  71. Coryphopterus thrix
  72. Cosmocampus albirostris
  73. Cryptotomus roseus
  74. Ctenogobius saepepallens
  75. Dactylopterus volitans
  76. Decapterus macarellus
  77. Dermatolepis inermis
  78. Diapterus auratus
  79. Diodon holocanthus
  80. Diodon hystrix
  81. Diplectrum formosum
  82. Diplectrum radiale
  83. Diplodus argenteus
  84. Doratonotus megalepis
  85. Dules auriga
  86. Echeneis naucrates
  87. Echidna catenata
  88. Elacatinus figaro
  89. Elacatinus phthirophagus
  90. Elacatinus pridisi
  91. Emblemariopsis
  92. Emblemariopsis signifer
  93. Enchelycore anatina
  94. Enchelycore nigricans
  95. Engraulis anchoita
  96. Epinephelus adscensionis
  97. Epinephelus itajara
  98. Epinephelus marginatus
  99. Epinephelus morio
  100. Equetus lanceolatus
  101. Eucinostomus
  102. Eucinostomus argenteus
  103. Eucinostomus melanopterus
  104. Eugerres
  105. Euthynnus alletteratus
  106. Fistularia petimba
  107. Fistularia tabacaria
  108. Gerres cinereus
  109. Ginglymostoma cirratum
  110. Gnatholepis thompsoni
  111. Gobioclinus kalisherae
  112. Gramma brasiliensis
  113. Gymnothorax funebris
  114. Gymnothorax miliaris
  115. Gymnothorax moringa
  116. Gymnothorax vicinus
  117. Haemulon atlanticus
  118. Haemulon aurolineatum
  119. Haemulon chrysargyreum
  120. Haemulon melanurum
  121. Haemulon parra
  122. Haemulon plumierii
  123. Haemulon squamipinna
  124. Halichoeres bivittatus
  125. Halichoeres brasiliensis
  126. Halichoeres dimidiatus
  127. Halichoeres penrosei
  128. Halichoeres poeyi
  129. Halichoeres radiatus
  130. Halichoeres rubrovirens
  131. Halichoeres sazimai
  132. Harengula clupeola
  133. Harengula jaguana
  134. Hemiramphus brasiliensis
  135. Heteropriacanthus cruentatus
  136. Hippocampus reidi
  137. Holacanthus ciliaris
  138. Holacanthus tricolor
  139. Holocentrus adscensionis
  140. Hypanus berthalutzae
  141. Hypleurochilus
  142. Hypleurochilus fissicornis
  143. Hypleurochilus pseudoaequipinnis
  144. Hyporthodus niveatus
  145. Hypsoblennius invemar
  146. Kyphosus
  147. Kyphosus cinerascens
  148. Kyphosus sectatrix
  149. Kyphosus vaigiensis
  150. Labrisomus cricota
  151. Labrisomus nuchipinnis
  152. Lactophrys trigonus
  153. Lutjanus alexandrei
  154. Lutjanus analis
  155. Lutjanus cyanopterus
  156. Lutjanus griseus
  157. Lutjanus jocu
  158. Lutjanus synagris
  159. Malacanthus plumieri
  160. Malacoctenus brunoi
  161. Malacoctenus delalandii
  162. Malacoctenus lianae
  163. Melichthys niger
  164. Microgobius carri
  165. Microspathodon chrysurus
  166. Mugil
  167. Mugil curema
  168. Mulloidichthys martinicus
  169. Muraena
  170. Muraena melanotis
  171. Muraena pavonina
  172. Mycteroperca
  173. Mycteroperca acutirostris
  174. Mycteroperca bonaci
  175. Mycteroperca interstitialis
  176. Mycteroperca microlepis
  177. Mycteroperca venenosa
  178. Myrichthys breviceps
  179. Myrichthys ocellatus
  180. Myripristis jacobus
  181. NA
  182. Narcine brasiliensis
  183. Negaprion brevirostris
  184. Nicholsina usta
  185. Ocyurus chrysurus
  186. Odontoscion dentex
  187. Ogcocephalus vespertilio
  188. Ophioblennius trinitatis
  189. Opistognathus aurifrons
  190. Orthopristis ruber
  191. Pagrus pagrus
  192. Parablennius
  193. Parablennius marmoreus
  194. Parablennius pilicornis
  195. Paraclinus spectator
  196. Paranthias furcifer
  197. Pareques acuminatus
  198. Pempheris schomburgkii
  199. Pinguipes brasilianus
  200. Platybelone argalus
  201. Pomacanthus arcuatus
  202. Pomacanthus paru
  203. Porichthys porosissimus
  204. Priacanthus arenatus
  205. Prognathodes brasiliensis
  206. Prognathodes guyanensis
  207. Prognathodes obliquus
  208. Pronotogrammus martinicensis
  209. Pseudocaranx dentex
  210. Pseudupeneus maculatus
  211. Ptereleotris randalli
  212. Rachycentron canadum
  213. Rhinobatos
  214. Rhomboplites aurorubens
  215. Rypticus bistrispinus
  216. Rypticus saponaceus
  217. Sardinella brasiliensis
  218. Sargocentron bullisi
  219. Scartella cristata
  220. Scarus trispinosus
  221. Scarus zelindae
  222. Scomberomorus maculatus
  223. Scorpaena
  224. Scorpaena brachyptera
  225. Scorpaena isthmensis
  226. Scorpaena plumieri
  227. Scorpaenodes caribbaeus
  228. Selene vomer
  229. Seriola dumerili
  230. Seriola lalandi
  231. Seriola rivoliana
  232. Serranus
  233. Serranus atricauda
  234. Serranus baldwini
  235. Serranus flaviventris
  236. Serranus phoebe
  237. Sparisoma
  238. Sparisoma amplum
  239. Sparisoma axillare
  240. Sparisoma frondosum
  241. Sparisoma radians
  242. Sparisoma rocha
  243. Sparisoma tuiupiranga
  244. Sphoeroides camila
  245. Sphoeroides greeleyi
  246. Sphoeroides testudineus
  247. Sphyraena
  248. Sphyraena barracuda
  249. Sphyraena borealis
  250. Sphyraena guachancho
  251. Sphyraena picudilla
  252. Starksia
  253. Starksia brasiliensis
  254. Stegastes fuscus
  255. Stegastes pictus
  256. Stegastes rocasensis

Geographic Coverages

Sampling ranged from the Brazilian northernmost continental shelf reefs of Parcel de Manuel Luís at 0∘ 52′ S; 44∘ 15′ W (Castro & Pires, 2001) to the southernmost coastal rocky reefs of Santa Catarina’s coastal islands at 27∘ 50′ S; 48∘ 26′ W (Anderson et al., 2015; Fig. 1). This also included the four oceanic island groups (Saint Paul’s Rocks, 0∘ 54′ N; 29∘ 20′ W; Rocas Atoll, 3∘ 52′ S; 33∘ 48′ W; Fernando de Noronha Archipelago, 3∘ 51′ S; 32∘ 25′ W; and Trindade and Martin Vaz Island group, 20∘ 29′ S; 29∘ 19′ W).

Bibliographic Citations

Contacts

Renato Morais
originator
position: Post-doctoral fellow
IRD
FR
Carlos E. L. Ferreira
originator
position: Professor
Universidade Federal Fluminense
Sergio R. Floeter
originator
position: Professor
Universidade Federal de Santa Catarina
Juan P. Quimbayo
originator
position: Post-doctoral fellow
Universidade de São Paulo
Thiago C. Mendes
originator
position: Post-doctoral fellow
Universidade Federal Fluminense
BR
Guilherme O. Longo
originator
position: Post-doctoral fellow
Universidade Federal do Rio Grande do Norte
Cesar Augusto Marcelino Mendes Cordeiro
originator
position: Professor
Universidade Estadual do Norte Fluminense
Campos dos Goytacazes
Rio de Janeiro
BR
email: cesarcordeiro@uenf.br
userId: https://orcid.org/0000-0003-4960-4502
Renato Morais
metadata author
position: Post-doctoral fellow
IRD
FR
Cesar Augusto Marcelino Mendes Cordeiro
metadata author
position: Professor
Universidade Estadual do Norte Fluminense
Campos dos Goytacazes
Rio de Janeiro
BR
email: cesarcordeiro@uenf.br
userId: https://orcid.org/0000-0003-4960-4502
André L. Luza
metadata author
position: Post-doctoral fellow
Universidade Federal de Santa Maria
BR
Cesar Augusto Marcelino Mendes Cordeiro
user
position: Professor
Universidade Estadual do Norte Fluminense
Campos dos Goytacazes
Rio de Janeiro
BR
email: cesarcordeiro@uenf.br
userId: https://orcid.org/0000-0003-4960-4502
Sérgio R. Floeter
principal investigator
position: Professor
Universidade Federal de Santa Catarina
Florianópolis
Santa Catarina
BR
email: sergiofloeter@gmail.com
userId: http://scholar.google.com/citations?user=l756o04AAAAJ
Carlos E. L. Ferreira
principal investigator
position: Professor
Universidade Federal Fluminense
Niterói
Rio de Janeiro
BR
email: carlosferreira@id.uff.br
userId: http://www.researcherid.com/rid/J-2571-2012
Cesar Augusto Marcelino Mendes Cordeiro
administrative point of contact
position: Professor
Universidade Estadual do Norte Fluminense
Campos dos Goytacazes
Rio de Janeiro
BR
email: cesarcordeiro@uenf.br
userId: https://orcid.org/0000-0003-4960-4502
Carlos E. L. Ferreira
administrative point of contact
position: Professor
Universidade Federal Fluminense
BR
email: carlosferreira@id.uff.br
Sérgio R. Floeter
administrative point of contact
position: Professor
Universidade Federal de Santa Catarina
BR
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