DATA REPORT article

Front. Mar. Sci., 16 February 2024

Sec. Marine Biology

Volume 11 - 2024 | https://doi.org/10.3389/fmars.2024.1327438

Fish biodiversity of Courtown Cays, seaflower biosphere reserve (Colombian Caribbean): new records and an annotated checklist

  • 1. Instituto de Estudios en Ciencias del Mar, CECIMAR, Universidad Nacional de Colombia, Santa Marta, Colombia

  • 2. Laboratorio de Ictiología, Departamento de Biología, Universidad del Valle, Cali, Colombia

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Introduction

The Seaflower Biosphere Reserve (SFBR) is renowned for its remarkably diverse marine life, particularly its rich fish fauna. Several species inhabiting the reserve are under some threat category and there is no exclusive fish species inventory for Courtown Cays (Isla Cayo Bolívar), an atoll located in the southern part of this marine protected area where intense artisanal fishing activities are carried out and illegal fishing has increased since 2006. To address this situation and enhance our scientific understanding of the region’s marine life, a dataset is presented with information about the marine fish species found in this oceanic reef complex during the Seaflower Scientific Expedition 2022. A total of 223 species were registered, distributed in 31 orders and 57 families, with Serranidae (25 spp.) and Labridae (24 spp.) showing the highest species richness. Forty-three species are recorded for the first time in this locality and one of them is recorded for the first time in the SFBR. These results highlights the critical importance of safeguarding vulnerable ecosystems, particularly oceanic coral reefs, which harbor hundreds of species of ecological and economic value and provide numerous ecological and economic benefits. This emphasizes the need of protection and prompt sustainable use of these resources.

Methods

Study area and data collection

The Seaflower Biosphere Reserve (SFBR), created in 2000, is a protected marine area of great importance for the conservation of the natural and cultural heritage of the Archipelago of San Andres, Providencia, and Santa Catalina, covering approximately 180,000 km2. This reserve is home to around a quarter of the Caribbean ichthyofauna (Bolaños-Cubillos et al., 2015; Acero et al., 2019), constituting one of the main reasons for the protection and proper management of its natural richness. Courtown Cays (Isla Cayo Bolívar) are located in the southern part of the reserve, at 12° 22’ – 28’ N and 81° 25’ – 31’ W, has a total area of 50.3 km2 (Díaz et al., 2000) and is part of the complex of 10 islands, keys, banks, and shoals that give the archipelago its name.

Scientific research in this area began at the end of the 20th century (Mejía et al., 1998; Mejía and Garzón-Ferreira, 2000); Bolaños-Cubillos et al. (2015) synthesized the existing knowledge about the ichthyofauna up to that date, providing a list of species for the so-called “southern keys”, Albuquerque and Courtown Cays, based on a compilation of information obtained in previous expeditions, explorations and studies that used different methodologies. The National Plan for Scientific Expeditions carried out by the government of Colombia marked the starting point in the monitoring of these remote areas and the expedition carried out during 2022 allowed the generation of an exclusive list for Cayo Bolivar due to the lack of this information.

During the Seaflower Scientific Expedition between the 9th and the 21st September, 2022, data was collected through visual censuses in coral reef formations and seagrass beds. The diversity of environments and formations (shallow peripheral reef, lagoon terrace, consolidated reefs, seagrass meadows and continental slope) made of this island an interesting site to study. Explorations were made by four divers through SCUBA diving using a 30 min timed swim method at different depths (0-35 m) in different sites of the key (Figure 1A). Occurrences and counts were conducted for all the species observed along the reef complex. Some specimens were collected to verify their identity and later deposited in the ichthyology collection of the Universidad del Valle (CIRUV). To verify new records, the works of Bolaños-Cubillos et al. (2015); Acero et al. (2019) and Robertson and Van Tassell (2019) were used as a reference.

Figure 1

Figure 1

(A) Distribution of the sampling locations in Courtown Cays reef complex, Seaflower Biosphere Reserve. (AA). Geographical location of the study area. The solid line demarcates the marine protected area. (AB). Bottom characteristics and distribution of benthic categories in Courtown Cays (Allen Coral Atlas, 2022). (B) Families that contributed the most to new records in the study area. White numbers within the circle indicate the number of species recorded per family and the legend denote the percentages that each family contributes to the new records. (C) Families with the highest species richness in Courtown Cays reef complex. In green cryptic fishes and in blue families with fishes of commercial interest.

Data availability

The dataset “Fish biodiversity of Courtown Cays, Seaflower Biosphere Reserve (Colombian Caribbean): new records and an annotated checklist” was assembled using the Darwin Core standard (DwC) and is available through the Integrated Publishing Tool of the Ocean Biogeographic Imation System (OBIS) and the Global Biodiversity Information Facility (GBIF) Colombian nodes (SIBM-SIB Colombia). Links (Acero et al., 2023):

SiB Colombia: https://biodiversidad.co/data?datasetKey=75301af4-c7b0-4b93-818f-bdf5d7cdabe0

GBIF: https://www.gbif.org/dataset/75301af4-c7b0-4b93-818f-bdf5d7cdabe0

OBIS: https://obis.org/dataset/097332d5-d8af-4e83-9f02-4750c1e439c4

DOI: https://doi.org/10.15472/4a8ygj

Outcomes and discussion

A total of 223 species were recorded for Courtown Cays (Isla Cayo Bolivar) (Table 1). Exploring this atoll allowed us to observe one of the highest fish richness in the SFBR [Roncador: 140 spp.; Serrana: 155 spp.; Serranilla: 166 spp.; Providencia: 248 spp.; Albuquerque: 207 spp.; Courtown Cays (present study): 223 spp.], although we noticed low abundances of large bony predators, which are in turn of high commercial interest such as snappers, groupers and some parrotfishes. Yet, 48 (22%) of the recorded species are of commercial interest to local communities. Twenty-seven of the species observed (12%) have been assigned with some threat category by the International Union for Conservation of Nature (IUCN) and/or the regional assessment included in the Red Book of Marine Fishes of Colombia (Chasqui et al., 2017), and 43 (20%) species were new records for this location.

Table 1

Order and family Specie TC CI NR NRSF
CARCHARHINIFORMES
Carcharhinidae Carcharhinus perezii x x
Galeocerdo cuvier x x
Negaprion brevirostris x x
Rhizoprionodon sp. x x x
Sphyrnidae Sphyrna mokarran x x x
ORECTOLOBIFORMES
Ginglymostomatidae Ginglymostoma cirratum x
MYLIOBATIFORMES
Dasyatidae Hypanus americanus x x
Myliobatidae Aetobatus narinari x x
ANGUILIFORMES
Muraenidae Enchelycore nigricans
Gymnothorax funebris
Gymnothorax miliaris
Gymnothorax moringa
Congridae Heteroconger longissimus
Ophichthidae Myrichthys breviceps
CLUPEIFORMES
Clupeidae Jenkinsia sp
AULOPIFORMES
Synodontidae Synodus intermedius
Synodus synodus
HOLOCENTRIFORMES
Holocentridae Holocentrus adscensionis
Holocentrus rufus
Myripristis jacobus
Neoniphon marianus
Sargocentron vexillarium
SCOMBRIFORMES
Scombridae Thunnus atlanticus x
SYNGNATHIFORMES
Aulostomidae Aulostomus maculatus
Dactylopteridae Dactylopterus volitans
Mullidae Mulloidichthys martinicus
Pseudupeneus maculatus
Syngnathidae Cosmocampus elucens x
GOBIIFORMES
Gobiidae Coryphopterus dicrus
Coryphopterus eidolon x
Coryphopterus glaucofraenum
Coryphopterus personatus x
Coryphopterus thrix x x
Coryphopterus tortugae x x
Ctenogobius saepepallens x
Gnatholepis thompsoni
Elacatinus evelynae
Elacatinus horsti
Elacatinus lori x
Elacatinus louisae x
Elacatinus prochilos x x
Priolepis hipoliti
Ptereleotris helenae x
Risor ruber x
KURTIFORMES
Apogonidae Apogon conklini
Apogon maculatus
Apogon robbyi x
Astrapogon puncticulatus x
Phaeoptyx sp.
INCERTAE SEDIS – CARANGARIA
Sphyraenidae Sphyraena barracuda x
Sphyraena borealis x x
CARANGIFORMES
Carangidae Alectis ciliaris x
Caranx bartholomaei x
Caranx crysos x
Caranx latus x
Caranx lugubris x
Caranx ruber x
Decapterus tabl x x x
Elagatis bipinnulata x
Selar crumenophthalmus x
Seriola rivoliana x
Trachinotus goodei x
Trachinotus falcatus x
Coryphaenidae Coryphaena hippurus x
Echeneidae Echeneis naucrates
Echeneis neucratoides x
PLEURONECTIFORMES
Bothidae Bothus lunatus
INCERTAE SEDIS – OVALENTARIA
Grammatidae Gramma loreto
Gramma melacara
Opistognathidae Opistognathus aurifrons
Opistognathus maxillosus
Opistognathus whitehursti x
Pomacentridae Abudefduf saxatilis
Azurina cyanea
Azurina multilineata
Chromis insolata
Microspathodon chrysurus
Stegastes adustus
Stegastes diencaeus
Stegastes leucostictus
Stegastes partitus
Stegastes planifrons
Stegastes xanthurus
BELONIFORMES
Belonidae Strongylura timucu x
Tylosurus crocodrilus x
Exocoetidae Exocoetus sp.
Hemiramphidae Hemiramphus balao
BLENNIIFORMES
Blenniidae Entomacrodus nigricans
Ophioblennius macclurei
Chaenopsidae Acanthemblemaria aspera x
Acanthemblemaria maria x
Acanthemblemaria spinosa
Chaenopsis sp. x
Emblemaria pandionis x
Emblemariopsis sp.
Lucayablennius zingaro
Labrisomidae Gobioclinus bucciferus
Gobioclinus kalisherae x
Malacoctenus aurolineatus x
Malacoctenus boehlkei
Malacoctenus erdmani
Malacoctenus gilli
Malacoctenus macropus
Malacoctenus triangulatus
Tripterygiidae Enneanectes boehlkei
INCERTAE SEDIS – EUPERCARIA
Malacanthidae Malacanthus plumierii
Pomacanthidae Centropyge argi x
Holacanthus ciliaris
Holacanthus tricolor
Pomacanthus arcuatus
Pomacanthus paru
Sciaenidae Eques punctatus
GERREIFORMES
Gerreidae Eucinostomus sp. x
LABRIFORMES
Labridae Bodianus rufus
Clepticus parrae
Halichoeres bivittatus
Halichoeres cyanocephalus x
Halichoeres garnoti
Halichoeres maculipinna
Halichoeres pictus x
Halichoeres poeyi x
Halichoeres radiatus
Lachnolaimus maximus x x
Scarus coelestinus x
Scarus guacamaia x
Scarus iseri
Scarus taeniopterus
Scarus vetula x
Sparisoma atomarium
Sparisoma aurofrenatum
Sparisoma chrysopterum
Sparisoma radians
Sparisoma rubripinne
Sparisoma viride x
Thalassoma bifasciatum
Xyrichtys martinicensis x
Xyrichtys splendens
CHAETODONTIFORMES
Chaetodontidae Chaetodon capistratus
Chaetodon ocellatus
Chaetodon sedentarius
Chaetodon striatus
Prognathodes aculeatus
ACANTHURIFORMES
Acanthuridae Acanthurus chirurgus
Acanthurus coeruleus
Acanthurus tractus
LUTJANIFORMES
Haemulidae Anisotremus surinamensis
Anisotremus virginicus
Brachygenys chrysargyreum
Haemulon album x
Haemulon aurolineatum
Haemulon carbonarium
Haemulon flavolineatum
Haemulon macrostomum x
Haemulon melanurum x
Haemulon parra x
Haemulon plumierii x
Haemulon sciurus x
Haemulon vittatum
Lutjanidae Apsilus dentatus x
Lutjanus analis x x
Lutjanus apodus x
Lutjanus buccanella x x
Lutjanus griseus x
Lutjanus jocu x x
Lutjanus mahogoni x
Lutjanus synagris x x
Lutjanus chrysurus x x
LOBOTIFORMES
Lobotidae Lobotes surinamensis
SPARIFORMES
Sparidae Calamus bajonado
Calamus calamus
PRIACANTHIFORMES
Priacanthidae Heteropriacanthus cruentatus
LOPHIIFORMES
Antennariidae Antennarius pauciradiatus x
TETRAODONTIFORMES
Balistidae Balistes capriscus
Balistes vetula x x x
Canthidermis maculata
Canthidermis sufflamen x
Melichthys niger
Diodontidae Diodon holocanthus
Diodon hystrix
Xanthichtys ringens x
Monacanthidae Aluterus scriptus
Cantherines macrocerus
Cantherines pullus
Monacanthus tuckeri
Ostraciidae Acanthostracion polygonius
Acanthostracion quadricornis
Lactophrys bicaudalis
Lactophrys trigonus
Lactophrys triqueter
Tetraodontidae Canthigaster rostrata
Sphoeroides spengleri
PEMPHERIFORMES
Pempheridae Pempheris schomburgkii
CENTRARCHIFORMES
Cirrhitidae Amblycirrhitus pinos
Kyphosidae Kyphosus cinerascens x
Kyphosus vaigiensis
PERCIFORMES
Serranidae Cephalopholis cruentata x
Cephalopholis fulva x
Diplectrum bivittatum
Epinephelus guttatus x
Hypoplectrus aberrans
Hypoplectrus affinis x
Hypoplectrus guttavarius
Hypoplectrus indigo
Hypoplectrus maculiferus x
Hypoplectrus nigricans
Hypoplectrus providencianus x
Hypoplectrus puella
Hypoplectrus randallorum x
Hypoplectrus unicolor
Liopropoma rubre
Mycteroperca bonaci x x
Mycteroperca interstitialis x x
Mycteroperca tigris x x
Mycteroperca venenosa x x
Serranus baldwini x
Serranus tabacarius
Serranus tigrinus
Serranus tortugarum x
Rypticus saponaceus
Schultzea beta x
Scorpaenidae Pterois volitans
Scorpaena cf. albifimbria
Scorpaena plumieri

Inventory of the species observed in Cayo Bolivar during the Seaflower Scientific Expedition 2022.

Species under some threat category: TC; species of commercial interest: CI; new record for the locality: NR; new record for the SFBR: NRSF.

The most abundant families were Serranidae (11%), Labridae (11%), Gobiidae (7%), Haemulidae (6%), Carangidae (5%), and Pomacentridae (5%), with other families representing less than 5% of the total fish richness (Figure 1B). Families Serranidae, Labridae, Haemulidae and Carangidae have species of commercial interest, which therefore highlights the crucial role and potential of these areas in the conservation of fish stocks.

Pomacentridae is one of the most abundant families that can be found in the Caribbean Sea assemblages and are characterized by its numerical dominance of small bodied species and broader distribution (Seeman et al., 2018). Other studies carried out in the Caribbean have found similar results, with this being one of the most recorded fish families (Dominici-Arosemena and Wolff, 2005; Alemu, 2014; Andradi-Brown et al., 2016).

Gobiidae was the third richest family in the study and contributed with 16 species. Other families of cryptic fishes, such as Chaenopsidae and Labrisomidae, were also significant as they represent 33% of the new records of this study (Figure 1C). A large proportion of tropical reef fish diversity is composed of cryptobenthic fishes: bottom-dwelling, morphologically or behaviorally cryptic species typically less than 50 mm in length (Depczynski and Bellwood, 2003). Their small body size allowed them to diversify at high rates exploiting small microhabitats and develop a wide range of life-history adaptations. However, despite their diversity and abundance, these fishes are poorly studied, overlooked and an underestimated component due to their small size, difficult identification, and cryptic habits (Herler et al., 2011). Since the information about the geographic coverage of cryptobenthic fishes is poor, this emphasizes the remarkable reservoir of biodiversity that is yet to be discovered (Brandl et al., 2018). On the other hand, the crucial ecological role of this community of fishes in coral reef trophodynamics is of great value (Bellwood et al., 2012; Goatley et al., 2016; Brandl et al., 2019) and makes necessary to apply greater efforts to study this “hidden half” of the vertebrate biodiversity on coral reefs (Brandl et al., 2018).

The high number of new records calls upon the need to continue the exploration and monitoring on remote localities and join research efforts to expand knowledge about the ecology, systematics, and conservation of understudied groups. Most of the new records may be due to reduced methodologies, limitations in sampling and few studies previously carried out in this location. The two new records of sharks were provided by Diego Cardeñosa, who carried out a study using baited remote underwater videos BRUVS. The use of this methodology different from the classic visual censuses has been found to be especially effective at observing predatory and mobile species, such as elasmobranchs, since the behaviour of many fish changes in the presence of divers (Watson and Harvey, 2007).

In the case of the cherubfish Centropyge argi, the yellowcheek wrasse Halichoeres cyanocephalus, the sargassum triggerfish, Xanthichthys ringens, the school bass Schultzea beta and the chalk bass Serranus tortugarum it has been found that they are only present at depths greater than 30 m or are more abundant in deep environments (Randall, 1963; Colin, 1974; Moyer et al., 1983; Weaver et al. 2006; Robertson and Van Tassell, 2019) so they appear to be indicator species of mesophotic habitats (García-Sais, 2010) and are difficult species to census since depth becomes a limitation when carrying out studies through autonomous diving. Other species such as the rosy razorfish Xyrichtys martinicensis may have gone unnoticed previously since they do not actually live in coral reefs, but rather in sandy bottoms or near seagrass meadows.

These results place these small key as a strategic point in the conservation of the ichthyic fauna of the SFBR, as well as of the Greater Caribbean. However, despite the species richness found, the observed abundances indicated the presence of only a few representatives of fish families of high-body sizes and of commercial interest mainly because they are targeted by artisanal fishermen and illegal fishing. Therefore, it is imperative to direct efforts for the protection, monitoring, control and surveillance of these localities that are little studied but intensively exploited.

Statements

Data availability statement

The dataset “Fish biodiversity of Courtown Cays, Seaflower Biosphere Reserve (Colombian Caribbean): new records and an annotated checklist” was assembled using the Darwin Core standard (DwC) and is available through the Integrated Publishing Tool of the Ocean Biogeographic Imation System (OBIS) and the Global Biodiversity Information Facility (GBIF) Colombian nodes (SIBM-SIB Colombia). Links (Acero et al., 2023):

SiB Colombia: https://biodiversidad.co/data?datasetKey=75301af4-c7b0-4b93-818f-bdf5d7cdabe0

GBIF: https://www.gbif.org/dataset/75301af4-c7b0-4b93-818f-bdf5d7cdabe0

OBIS: https://obis.org/dataset/097332d5-d8af-4e83-9f02-4750c1e439c4

DOI: https://doi.org/10.15472/4a8ygj

Ethics statement

The animal study was approved by Ministerio de Ambiente y Desarrollo Sostenible. The study was conducted in accordance with the local legislation and institutional requirements.

Author contributions

AP-S: Conceptualization, Data curation, Formal analysis, Investigation, Validation, Writing – original draft. NO: Investigation, Methodology, Validation, Writing – review & editing. NR: Validation, Writing – review & editing. JT: Data curation, Investigation, Methodology, Validation, Writing – review & editing. AA: Conceptualization, Data curation, Funding acquisition, Investigation, Methodology, Project administration, Supervision, Validation, Writing – original draft.

Funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This workwas supported by Universidad Nacional de Colombia – Sede Caribe, Universidad del Valle and the Colombian Ocean Commission –CCO [for its Spanish initials]. The publication of this manuscript was financially supported by the Ministry of Science, Technology and Innovation through the Colombia Bio Program, the Corporation Center of Excellence in Marine Sciences – CEMarin and the Colombian Ocean Commission through the special cooperation agreement No. 80740-026-2022.

Acknowledgments

The Colombian Ocean Commission who lead the National Plan for Scientific Expeditions, the Instituto de Estudios en Ciencias del Mar (CECIMAR), Universidad Nacional de Colombia - Sede Caribe and Universidad del Valle for their contribution to the logistics and development of this project. To Diego Cardeñosa for the records provided from his project and to Edgardo Londoño for its support in taking photographs of the specimens

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmars.2024.1327438/full#supplementary-material

Supplementary Figure 1

Fishes observed and/or collected during the Seaflower Scientific Expedition 2022. (A)Acanthemblemaria spinosa. (B)Acanthemblemaria maria. (C)Emblemaria pandionis female. (D)Elacatinus louisae. (E)Coryphopterus tortugae.(F)Gobioclinus kalisherae.(G)Canthidermis maculata and Lobotes surinamensis.

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Summary

Keywords

fish species, inventory, new records, seaflower biosphere reserve, Courtown Cays

Citation

Puentes-Sayo A, Ossa N, Rivas N, Tavera J and Acero P A (2024) Fish biodiversity of Courtown Cays, seaflower biosphere reserve (Colombian Caribbean): new records and an annotated checklist. Front. Mar. Sci. 11:1327438. doi: 10.3389/fmars.2024.1327438

Received

25 October 2023

Accepted

29 January 2024

Published

16 February 2024

Volume

11 - 2024

Edited by

Sabrina Lo Brutto, University of Palermo, Italy

Reviewed by

Randa Mejri, University of Sfax, Tunisia

Branko Dragičević, Institute of Oceanography and Fisheries (IZOR), Croatia

Updates

Copyright

*Correspondence: Alejandra Puentes-Sayo,

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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