Short Communication
Print
Short Communication
First report of crested cusk-eel, Ophidion josephi (Actinopterygii: Ophidiiformes: Ophidiidae), in the southwestern Gulf of Mexico
expand article infoLuis Fernando Del Moral-Flores, Janeth Rodríguez-González, María de Lourdes Jiménez-Badillo§
‡ Universidad Nacional Autónoma de México, Mexico City, Mexico
§ Universidad Veracruzana, Boca del Río, Mexico
Open Access

Abstract

The crested cusk-eel, Ophidion josephi Girard, 1858, is a coastal marine species that is distributed in the northwestern Atlantic, from the northern Gulf of Mexico to Georgia, USA. Eighteen specimens (177–230 mm in standard length) were caught by beach purse seine at a depth of about 5 m, in Veracruz, in the southwestern Gulf of Mexico. This is the first documentation from Mexican marine waters and the southernmost confirmed records of this species, showing that its range extends further south than previously known and that it shares faunistic similarities with other species in the northwestern Atlantic.

Keywords

distribution, marine fish, morphometric, Mexico, new record, range extension

Introduction

The family Ophidiidae comprises four subfamilies and 280 valid species. The subfamily Ophidiinae contains 65 species (Fricke et al. 2022). Ophidiid fishes are characterized by having supramaxillary, dorsal fin rays usually equal to or longer than opposing anal-fin rays, scales present on body, pelvic fins rarely absent, when they are present with one or two soft rays (Cohen and Nielsen 1978; Nelson et al. 2016). Cusk eels have a wide distribution around the world in tropical, subtropical and temperate seas. The majority of species are coastal, mainly in the continental shelf, although many are found in deep waters, reaching 7965 m (Gerringer et al. 2021). In the western Atlantic, this family is represented by 26 genera and about 68 species (Nielsen and Robins 2002; Garrido-Linares and Acero-P. 2006). However, the limits of several species in both the southern and northern parts have not been clarified yet.

This genus Ophidion Linnaeus, 1758 is found nearly worldwide in warm-temperate and tropical coastal and shelf waters. The largest number of species is concentrated on both coasts of America (Matallanas and Casadevall 1999). A taxonomic revision of the genus Ophidion is necessary; there are several characters that are shared with other genera (Cohen and Nielsen 1978; Lea and Robins 2003). It is considered a paraphyletic group and its relation with other clades is unclear (Nielsen et al. 1999). This genus is diagnosed by the following combination of characters: scales absent from sides and top of head; scales on body elongated, arranged in a basketweave or anguilloid pattern; ethmoid spine absent, or, if present, slender and anteriorly directed at its tip; total vertebrae 63 to 79; abdominal vertebrae 15 to 18; rays of each pelvic fin unequal in length; dorsal fin rays 129 to 150; anal fin rays 104 to 127; developed rakers on first gill arch 4 to 7 (Cohen and Nielsen 1978; Nielsen et al. 1999; Carnevale and Johnson 2015). Within them, the systematic and biogeographic review of the Ophidion marginatumjosephi complex is suggested and needed (Lea and Robins 2003), to understand the delimitation of species in their distribution areas. This group is characterized by having similarities of characters in early life history stages, such as an elongate body that becomes laterally compressed with development, the proportion of two or three pterygiophores per interneural space, the fact that the preanal length is short, and that the vertebrae ossify from both the anterior and posterior ends toward the middle (Fahay 1992; Fahay and Hare 2003).

In some species, there have been taxonomic problems. For example, Robins and Ray (1986) considered Ophidion welshi (Nichols et Breder, 1922) as a valid species. Later, Nielsen et al. (1999) considered it as a probable synonym. Finally, Nielsen and Robins (2002) indicate that it is a synonym for the crested cusk-eel, Ophidion josephi Girard, 1858. The latter is a coastal benthic species that is distributed in the northwestern Atlantic, from Georgia to northeastern Florida through the northern Gulf of Mexico (coastal bays to 55 m depth) (Nielsen et al. 1999; Fahay and Hare 2003). However, its southern distribution limit is unknown. This work describes a new and thus far southernmost record of O. josephi based on morphometrics and meristic characters.

Materials and methods

During four fishing events (15 November 2018, 15 November 2019, 18 October 2020, and 27 September 2021), 18 specimens of Ophidion josephi were captured by an artisanal fisherman from Las Barrancas community (19°0′24″N, 095°57′52″W), in Veracruz, the southwestern Gulf of Mexico (Fig. 1). The specimens were captured by beach purse seine between about 3 to 5 m of depth. The specimens were identified following the keys of Hoese and Moore (1998) and McEachran and Fechhelm (1998). Morphometric measurements expressed in proportion to the standard (SL%) and cephalic lengths (HL %) were carried out on the fresh specimen with electronic calipers to the nearest 0.1 mm according to Nielsen et al (1999). Sex was determined by the presence of the typical supraoccipital crest in males and its absence in females (Courtenay 1971). The meristic count was conducted on five specimens, which were cleared and differentially stained with alizarin red S and Alcian blue (Kelly and Bryden 1983) and by X-ray. The samples were fixed in 10% buffered formaldehyde, preserved in 70% ethyl alcohol, and deposited in the Ichthyological Collection of the Facultad de Estudios Superiores Iztacala (CIFI).

Figure 1. 

Distribution of Ophidion josephi in the Western Atlantic, including previous records (circles) obtained from GBIF (2021), and new records (diamond).

Results

Systematic account

Order Ophidiiformes

Family Ophidiidae

Subfamily Ophidiinae

Genus Ophidion Linnaeus, 1758

Ophidion josephi Girard, 1858

Fig. 2; Table 1

New records

MEXICO • 7 specimens (177–212 mm SL); Las Barrancas, Alvarado, Veracruz; 19°00′24′′N, 095°57′52′′W; 15 Nov. 2018; Pedro Ramon Roman leg.; CIFI–222 • 5 specimens (198–213 mm SL); Las Barrancas, Alvarado, Veracruz; 19°00′24′′N, 095°57′52′′W; 15 Nov. 2019; Pedro Ramon Roman leg.; CIFI–1417 • 5 cleared specimens (182–230 mm SL); Las Barrancas, Alvarado, Veracruz; 19°00′24′′N, 095°57′52′′W; 18 Oct. 2020; Pedro Ramon Roman leg.; CIFI 1649 • 1 specimen (198 mm SL); Las Barrancas, Alvarado, Veracruz; 19°00′24′′N, 095°57′52′′W; 27 Sep. 2021; Pedro Ramon Roman leg.; CIFI–1907.

Identification

The Mexican specimens of Ophidion josephi measured 177–213 mm SL and weighed 40.0–67.5 g (Fig. 2). The morphometric and meristic data are reported in Tables 1 and 2, respectively.

Table 1.

Morphometrics measurements expressed as proportion to the standard length (SL) and head length (HL) of Ophidion josephi collected in the southwestern Gulf of Mexico.

Character CIFI–222 (n = 7) CIFI–1417 (n = 5) CIFI–1907 (n = 1)
Weight [g] 40.0–67.5 43.5–60.2 55.3
Total length [mm] 180–215 201–218 201
Standard length [mm] 177–212 198–213 198
In %SL
Body depth 13.3–16.3 12.7–15.9 13.5
Head depth 12.1–13.8 11.3–12.9 11.8
Head length 17.9–19.5 18.0–19.3 19.0
Depth at dorsal fin 13.6–16.1 13.0–15.7 13.0
Depth at anal fin 12.4–13.7 11.5–13.7 12.8
Preanal length 39.0–41.8 37.2–39.0 37.6
Predorsal length 24.7–27.4 25.7–27.0 26.4
Prepectoral length 15.4–17.8 15.4–17.1 16.0
Prepelvic length 5.0–6.9 4.7–6.0 5.5
Dorsal fin base 72.3–75.0 71.9–74.5 72.7
Anal fin base 57.6–61.3 59.1–62.1 62.1
Pectoral fin length 10.6–16.3 11.0–13.3 13.3
Pelvic fin length 6.6–15.4 13.9–16.1 16.1
Postorbital length 10.2–11.8 10.5–11.8 10.6
Eye length 3.3–4.3 3.2–4.0 3.5
In %HL
Snout length 18.3–21.0 20.0–23.3 20.5
Interorbital width 16.9–20.9 15.2–16.6 16.5
Eye length 18.4–24.1 16.7–21.1 18.6
Upper jaw length 40.3–44.7 39.6–43.0 39.6
Table 2.

Meristic counts of five specimens of Ophidion josephi (182–230 mm SL) collected in the southwestern Gulf of Mexico (CIFI–1649).

Character CIFI–1649 CIFI–1649 CIFI–1649 CIFI–1649 CIFI–1649
(1) female (2) female (3) male (4) male (5) female
Caudal fin 9 9 9 9 9
Pectoral fin 23 21 21 22 22
Pelvic fin 2 2 2 2 2
Dorsal fin 142 139 139 147 142
Anal fin 115 108 112 117 115
Branchiostegal rays 7 7 7 7 7
Gill rakers (upper–lower) 2 + 4 2 + 4 2 + 4 2 + 4 2 + 4
Vertebrae (thoracic–caudal) 16 + 50 16 + 51 15 + 52 15 + 51 16 + 52
Figure 2. 

The Mexican specimen of Ophidion josephi, CIFI–222. A) An adult female, 181 mm SL. B) An adult male, 212 mm SL, the arrow points to the typical supraoccipital ridge of males. C) Arrangements of scales in body side. D) Radiographs of three specimens, 182–230 mm SL (CIFI-1949).

Description

Dorsal fin rays: 139–147; anal fin rays: 108–117; pectoral fin rays: 21–23; pelvic fin rays: 2; caudal fin rays: 9; branchiostegal 7; gill rakers total: 7; and trunk vertebrae total 16, and caudal vertebrae number 50 to 52. Elongate body covered with diminutive elongated cycloid scales, except for cephalic region. Identified by following combination of characteristics: short blunt snout (3.3%–4.4% of SL), slightly subterminal mouth, maxilla ending behind orbital margin. Moderate eye size, its length approximating that of snout (3.3%–4.3% SL). Five to four gill rakers on lover limb. Head length 17.9%–19.5% SL, with straight dorsal profile or in males strong crest, in straight line over preopercular region. Strong supraopercular spine covered by dermal fold. Pectoral fins shorter than head (57.5%–70% HL), round in shape, its coloration intense yellow, and in some cases, black. Distal margin of dorsal and anal fin black; that of anal fin wider. Predorsal fin length 24.7% to 27.4% in SL and its origin on middle part of pectoral fin. Yellow body coloration, some brown regions. Ventral part slightly lighter that dorsal one. Base of dorsal fin black along its entire length, becoming fainter near caudal fin. Three rows of dark spots on sides, upper one continuous, remaining ones interrupted and blurred. Body covered with cycloid and elongate scales, having basket-shaped pattern.

Diagnosis

This species is distinguished from its congeners by having three to four rows of spots usually fused into a solid stripe, with a distinct crest on the spots; and a swollen nape or crest.

Discussion

Ophidion josephi is a common species found in shallow coastal waters, which inhabits soft bottoms. It is the second most abundant cusk-eel in the bycatch of shrimp fishing (Hoese and Moore 1998). It has a narrow depth range of 9–55 m (Fahay and Hare 2003); spawn in the fall, has a rapid growth rate, and lives at least 27 months (Retzer 1991; Kells and Carpenter 2011).

The lack of detailed taxonomic sampling and analysis of the ichthyofauna in Mexican littorals is a possible cause of the absence of valid records of the species in the study area. However, Bautista-Hernández et al. (2001) mentioned Ophidion welshi, a synonym of O. josephi, as a species that is usually caught as a part of the bycatch of the sardine fishery practiced in the community of Las Barrancas, Veracruz. Chávez-López and Morán-Silva (2019) mentioned O. josephi as part of the incidental bycatch in shrimp fishing in the Campeche and estuarine zone or the Papalopan River. However, there is no valid record deposited in any collection. The presently reported study describes the finding of Ophidion josephi from the coast of Veracruz, Mexico which constitutes the southernmost record of this fish in the western Atlantic.

Information about their biology is unknown, but, like other species of Ophidion, they can be organisms that tend to bury themselves in the area during the day and leave their shelter at night to feed (Matallanas and Riba 1980). As the work of the fishermen begins during the day, it is unlikely that the organisms are captured.

Despite the similarity with the Caribbean, the biogeographic affinity of coastal and reef fish in the central-southern region of Veracruz also has a temperate affinity for the Carolinian Province (Del Moral-Flores et al. 2013). The warm-temperate Carolina Province contains a biogeographic area that is delimited into two sections: within the Gulf of Mexico, its limits are between Cabo Romano, Florida and Cabo Rojo, Mexico; and in the Atlantic section it is found between Cape Hatteras, North Carolina, and Cape Canaveral, Florida (Briggs and Bowen 2012). Larval dispersion can be a factor that does not allow to delimit a clear biogeographic barrier between the North and South of the Gulf of Mexico. In the Veracruz Reef System, near the area of this record, the oceanographic conditions, such as the presence of “nortes” (north winds) and the Campeche gyre (Salas-Pérez and Granados-Barba 2008) have an influence on larval diversity and abundance (Ayala-Rodríguez et al. 2016). Besides, it allows the establishment and extension of the range of distribution of various species of marine fish. This finding is relevant to understanding the geographic ranges of the species, a component of the Mexicana fauna.

Acknowledgments

We thank Mr Roman Ramón, a local fisherman who provided some of the specimens in this contribution, SNI–CONACyT for economic support, and the PAPITT–UNAM IA207820 project for the finance provided. Also to the anonymous reviewers for their helpful suggestions.

References

  • Ayala-Rodríguez GA, Ordóñez-López U, Meiners-Mandujano C, Marin-Hernández M (2016) Listado taxonómico, aspectos ecológicos y biogeográficos de las larvas de peces del Sistema Arrecifal Veracruzano, Suroeste del Golfo de México (junio 2011–junio 2013). Revista de Biología Marina y Oceanografía 51(2): 255–264. https://doi.org/10.4067/S0718-19572016000200004
  • Bautista-Hernández J, Chávez-López R, Franco-López J, Montoya-Mendoza J, Bedia-Sánchez C (2001) Ecología de la ictiofauna acompañante de la pesca ribereña en las Barrancas, Municipio de Alvarado, Veracruz. Revista de Zoología, UNAM 12: 12–27.
  • Carnevale G, Johnson GD (2015) A cretaceous cusk-eel (Teleostei, Ophidiiformes) from Italy and the Mesozoic diversification of percomorph fishes. Copeia 103(4): 771–791. https://doi.org/10.1643/CI-15-236
  • Chávez-López R, Morán-Silva A (2019) Revisión de la composición de especies de peces capturadas incidentalmente en la pesquería de camarón en el Golfo de México. Ciencia Pesquera 27(1): 65–82.
  • Cohen DM, Nielsen JG (1978) Guide to the identification of genera of the fish order Ophidiiformes with a tentative classification of the order. NOAA Technical Reports 417: 1–72. https://doi.org/10.5962/bhl.title.63242
  • Courtenay Jr WR (1971) Sexual dimorphism of the sound producing mechanism of the striped cusk-eel, Rissola marginata (Pisces: Ophidiidae). Copeia 1971(2): 259–268. https://doi.org/10.2307/1442826
  • Del Moral-Flores LF, Tello-Musi JL, Reyes-Bonilla H, Pérez-España H, Martínez-Pérez JA, Horta-Puga G, Velazco-Mendoza LA, Álvarez del Castillo-Cárdenas PA (2013) Lista sistemática y afinidades zoogeográficas de la ictiofauna del Sistema Arrecifal Veracruzano, México. Revista Mexicana de Biodiversidad 84(3): 825–846. https://doi.org/10.7550/rmb.34912
  • Fahay MP (1992) Development and distribution of cusk eel eggs and larvae in the middle Atlantic bight with a description of Ophidion robinsi n. sp. (Teleostei: Ophidiidae). Copeia 1992(3): 799–819. https://doi.org/10.2307/1446157
  • Fahay MP, Hare JA (2003) Preliminary guide to the identification of the early life history stages of ophidiiform fishes of the Western Central North Atlantic. NOAA Technical Memorandum NMFS–SEFSC– 520: 1–98.
  • Garrido-Linares M, Acero-P A (2006) Peces Ophidiiformes del Atlántico occidental tropical con especial énfasis en el mar Caribe colombiano. Biota Colombiana 7(2): 283–299.
  • Gerringer ME, Linley TD, Nielsen JG (2021) Revision of the depth record of bony fishes with notes on hadal snailfishes (Liparidae, Scorpaeniformes) and cusk eels (Ophidiidae, Ophidiiformes). Marine Biology 168(11): 167. https://doi.org/10.1007/s00227-021-03950-8
  • Global Biodiversity Infomation Facility (GBIF), Secretariat (2021) GBIF Backbone Taxonomy. Checklist dataset Ophidion josephi Girard, 1858, updated 15 May 2022. https://doi.org/10.15468/39omei
  • Hoese HD, Moore RH (1998) Fishes of the Gulf of Mexico: Texas, Louisiana, and adjacent waters. Texas A&M University Press, College Station, Texas, 422 pp.
  • Kells V, Carpenter K (2011) A field guide to coastal fishes from Maine to Texas. Johns Hopkins University Press, Baltimore, MD, USA, 447 pp.
  • Kelly WL, Bryden MM (1983) A modified differential stain for cartilage and bone in whole mount preparations of mammalian fetuses and small vertebrates. Biotechnic and Histochemistry 58(3): 131–134. https://doi.org/10.3109/10520298309066773
  • Lea RN, Robins CR (2003) Four new species of the genus Ophidion (Pisces: Ophidiidae) from the western Atlantic Ocean. University of Kansas Museum of Natural History. Scientific Papers 31: 1–9. https://doi.org/10.5962/bhl.title.8466
  • Matallanas J, Casadevall M (1999) Present day distribution and historical biogeography of the tribe Ophidiini (Ophidiiformes, Ophidiida, Ophidiinae) from the East Tropical Atlantic (CLOFETA area) and North-East Atlantic and Mediterranean (CLOFNAM area). Cahiers de Biologie Marine 40: 135–140.
  • Matallanas J, Riba G (1980) Aspectos biológicos de Ophidion barbatum Linnaeus, 1758 y O. rochei Muller, 1845 (Pisces, Ophidiidae) de la costa catalana. Investigaciones Pesqueras 44(3): 389–406.
  • McEachran J, Fechhelm JD (1998) Fishes of the Gulf of Mexico, Vol. 1. Myxiniformes to Gasterosteiformes. University of Texas, Austin, TX, USA, 1112 pp. https://doi.org/10.7560/752061
  • Nielsen JG, Robins CR (2002) Ophidiidae. Pp. 965–972. In: Carpenter KE (Ed.) The living marine resources of the Western Central Atlantic. Volume 2. Bony fishes Part 1 (Acipenseridae to Grammatidae). FAO Species Identification Guide for Fishery Purposes and American Society of Ichthyologist and Herpetologist Special Publication 5.
  • Nielsen JG, Cohen DM, Markle DF, Robins CR (1999) FAO Species Catalogue. Volume 18. Ophidiiform fishes of the world (Order Ophidiiformes). An annotated and illustrated catalogue of pearlfishes, cusk-eels, brotulas and other ophidiiform fishes known to date. FAO, Rome. FAO Fisheries Synopsis 125(18): 1–178.
  • Retzer ME (1991) Life-history aspects of four species of cusk-eels (Ophidiidae: Ophidiiformes) from the northern Gulf of Mexico. Copeia 1991(3): 703–710. https://doi.org/10.2307/1446396
  • Robins CR, Ray GC (1986) A field guide to Atlantic coast fishes of North America. Houghton Mifflin, Boston, MS, USA, 354 pp.
  • Salas-Pérez J, Granados-Barba A (2008) Oceanographic characterization of the Veracruz Reefs System. Atmosfera 21(3): 281–301.