RESEARCH NOTE

First record of humpback anglerfish (Melanocetus johnsonii) (Melanocetidae) in Antarctic waters

Alexei M. Orlov,^1,2 Svetlana Y. Orlova,³ Alexander A. Volkov³ & Dmitry V. Pelenev⁴

¹ Laboratory of Sea Fishes of the Russian Far East, Russian Federal Research Institute of Fisheries and Oceanography, 17, V. Krasnoselskaya St., Moscow 107140, Russia
² Laboratory for Ecology of Lower Vertebrates, A.N. Severtsov Institute of Ecology and Evolution of the Russian Academy of Sciences, 33, Leninsky Prospekt, Moscow 119071, Russia
³ Laboratory of Molecular Genetics, Russian Federal Research Institute of Fisheries and Oceanography, 17, V. Krasnoselskaya Sr., Moscow 107140, Russia
⁴ Laboratory of the Pacific Ocean Basin, Center of International Fisheries Cooperation, Russian Federal Research Institute of Fisheries and Oceanography, 17, V. Krasnoselskaya St., Moscow 107140, Russia

Abstract

The first record of the humpback anglerfish (Melanocetus johnsonii) in Antarctic waters (Ross Sea) is documented. Species identification is confirmed by the structure of the escal bulb and analysis of the mitochondrial cytochrome oxidase subunit I (COI) gene. This record extends the known range of M. johnsonii by more than 1000 nm to the south. The taxonomic status of Melanocetus species in Antarctic waters is discussed.

Keywords
Melanocetus sp.; new record; taxonomy; distribution; Ross Sea; Antarctic.

Correspondence
Alexei M. Orlov, 17, V. Krasnoselskaya St., Moscow, 107140, Russia. E-mail: orlov@vniro.ru

(Published: 6 March 2015)

Polar Research 2015. © 2015 A.M. Orlov et al. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Citation: Polar Research 2015, 34, 25356, http://dx.doi.org/10.3402/polar.v34.25356

According to modern concepts (Pietsch & Orr 2007; Pietsch 2009; Mia et al. 2010), the family of black seadevils (Melanocetidae) is represented by the single genus Melanocetus with six valid species: M. eustalis, M. johnsonii, M. murrayi, M. niger, M. polyactis and M. rossi. Two species—M. johnsoni and M. murrayi—are widely distributed in the Atlantic, Pacific and Indian oceans. Three other species—M. eustalis, M. niger and M. polyactis—are known only in the eastern tropical Pacific. It is believed that Antarctic waters of the Ross Sea are inhabited by the sixth representative of the genus—M. rossi (Pietsch 1990; Miller 1993; Balushkin & Fedorov 2002; Hanchet et al. 2013)—that was described from a single specimen in poor condition (Pietsch 2009). It had a standard length (SL) of 118 mm and had been caught by otter trawl at a depth of 390 m (Balushkin & Fedorov 1981). Morphological features suggest that M. rossi is very close to M. johnsonii and M. murrayi (Balushkin & Fedorov 2002). However, Pietsch (2009) suggests that M. rossi appears to be very similar to M. johnsonii and may well prove to be a synonym of this species.

This communication documents the first valid record of Melanocetus johnsonii Günther, 1864 in the Ross Sea and discusses the taxonomic status of Melanocetus species in Antarctic waters.

Materials and methods

A single specimen of the anglerfish genus Melanocetus with a total length (TL) of 157 mm (SL 133 mm) and body weight of 290 g (Fig. 1) was found in the stomach of an Antarctic toothfish (Dissostichus mawsoni) with a TL of 138 cm and a body weight of 28 kg, caught on 6 January 2014 by bottom longline (set no. 25) from the fishing vessel Ugulan at 1243–1355 m depth in the area with coordinates 75° 13.9′–75° 14.4′ S and 175° 05.2′–175° 20.4′ W (Fig. 2).

Fig. 1  Anglerfish of the Melanocetus genus from the stomach of an Antarctic toothfish captured in the Ross Sea, on 6 January 2014, from the FV Ugulan.

Fig. 2  The capture locations in the Ross Sea of the holotype of Melanocetus rossi (Balushkin & Fedorov 1981), the two specimens of M. rossi from the stomachs of Antarctic toothfish collected in 2013 (Hanchet et al. 2013) and our specimen from the stomach of an Antarctic toothfish collected in 2014.

For technical reasons, there was no opportunity to save and bring the angerfish to the laboratory. It was measured and photographed on board. A pectoral fin clip was cut for subsequent genetic analysis and the illicium was cut off for further morphological study (both fin clip and illicium were preserved in 96% ethanol at a ratio of 1:5). All measurements of illicium and escal bulb were taken according to previously published methods (Bertelsen 1951; Pietsch & Van Duzer 1980; Anderson & Leslie 2001; Pietsch 2009).

The preserved pectoral fin and illicium are registered and deposited in the Russian National Collection of Genetic Reference Materials in the Russian Federal Research Institute of Fisheries and Oceanography (Moscow) under a number MEL 0313.06.01. All molecular genetic studies—DNA extraction, polymerase chain reaction (PCR), PCR product purification and nucleotide sequencing—were performed using standard molecular genetic techniques (Ivanova et al. 2007). For the sequencing reaction, 0.3 pmol of the PCR product and 3.2 pmol of the appropriate primer were taken. Each PCR product was sequenced from both forward (F) and reverse (R) primers. DNA sequencing was performed on ABI Prism 3130xl device (Life Technologies, Carlsbad, CA, USA) according to the manufacturer's protocol. A set of universal primers was used for mitochondrial cytochrome oxidase subunit I (COI) gene amplification (Ivanova et al.2007). Data processing was performed, and a molecular genetic tree was constructed by using Geneious 6.0.5 software based on the neighbour joining method, Kimura 2-parameter model and 1000 bootstrap replicates (Kimura 1980). Analysis of genetic distances was conducted using the maximum composite likelihood model (Tamura et al. 2004) that involved nine nucleotide sequences. All positions containing gaps and missing data were eliminated. There were a total of 649 positions in the final data set. Evolutionary analyses were conducted in the MEGA6 software package (Tamura et al. 2013). Data on COI sequences of congeneric species were taken from the open BOLD database (http://www.boldsystems.org). Ceratias holboelli (Ceratiidae) was selected as an outgroup (Pietsch & Orr 2007; Mia et al. 2010).

Results and discussion

Morphometry

The study of the illicium of the Melanocetus specimen (Fig. 3) and comparison with those of other Melanocetus species verifies that the former belongs to the species M. johnsonii, whose esca is characterized by the existence of crests and a black pigmented area on the top (Fig. 4). Among other species of the genus, the esca of M. rossi bears a medial crest, but its top is not pigmented (Fig. 5). Pietsch (2009) pointed out that the esca of M. johnsonii bears anterior and posterior crests (see Fig. 4). However, there is a single crest in our specimen located in the central part of the escal top with the black pigmented area. Escas of M. polyactis and M. niger (Fig. 6) are also characterized by a black pigmented area on the top but there are no crests on the escae (Pietsch 2009).

Fig. 3  Two lateral views of the esca of an anglerfish of the genus Melanocetus from the stomach of an Antarctic toothfish collected in 2014 in the Ross Sea.

Fig. 4  Variations of escal form in Melanocetus johnsonii (after Pietsch & Van Duzer 1980).

Fig. 5  Esca of Melanocetus rossi (after Balushkin & Fedorov 1981).

Fig. 6  Variations of escal form in different Melanocetus species, from left to right: M. johnsonii, M. polyactis, M. niger and M. murrayi. (From Pietsch, Theodore W., Oceanic anglerfishes: extraordinary diversity in the deep sea. © 2009 by the Regents of the University of California. Published by the University of California Press.)

Relative sizes of illicium and esca are considered the main taxonomic features of anglerfishes (Bertelsen 1951; Pietsch & Van Duzer 1980; Pietsch 2009). The relative length of the illicium in our specimen (25.8% SL) is slightly smaller as compared with literature data (Table 1) for M. johnsonii (26.0–60.8%) and M. rossi (29.2%). The width of the escal bulb (2.7% SL) in our specimen falls outside of the range of known values for the species mentioned above: 4.3–9.2% and 3.6–3.7% SL, respectively. According to the relative sizes of the illicium and esca, our specimen is closest to M. murrayi, from which (apart from the shape of the vomer) it is differentiated by the existence of a crest and a black pigmented area of the top of the esca. Some of the difference of the escal size in our specimen is probably related to the preservation of the illicium in ethanol. The data provided here on the width of the esca suggest greater variability of this feature in M. johnsonii as compared to previously known information.

Genetic analysis

To reveal the species identity using genetic markers, the analysis of the COI gene was performed. Results of genetic analysis definitively confirm that our specimen (GenBank accession number is KM593294) is Melanocetus johnsonii. On the molecular genetic tree (Fig. 7), it forms a separate cluster (bootstrap within the cluster varies 62.7–99.9%) with other M. johnsonii specimens that differentiates well from congeneric species M. murrayi (bootstrap 100%). Genetic distance (Table 2) between our specimen and M. johnsonii (mean value for four specimens) is extremely low (unit of the number of base substitutions per site is 0.0015), which confirms its affiliation to Melanocetus johnsonii.

Fig. 7  Molecular genetic tree of selected anglerfish species based on the neighbour joining method, Kimura 2-parameter model and 1000 bootstrap replicates for mitochondrial cytochrome oxidase subunit I (COI) genes. Numbers beside each branch indicate bootstrap values above 50%. The scale bar is according to the Kimura 2-parameter model. Codes besides species names represent the GenBank accession numbers. Our specimen is indicated as Melanocetus sp.

Taxonomic and zoogeographic notes

As for the taxonomic status of M. rossi, we suggest that it would be premature to synonymize this species with M. johnsonii due to the need to examine additional materials (seven preserved specimens and tissue samples of four specimens from the Ross Sea) that are available at the Museum of New Zealand (A. Stewart, pers. comm.). Among all morphological features that differentiate M. rossi from M. johnsonii the colouration of the esca (lack of black pigment on the top) remains the most important since relative sizes of illicium and esca in M. rossi lie within the range of M. johnsonii, taking into account the measurements of the specimen reported here (see Table 1). Co-occurrence of two congeneric species (M. johnsonii and M. rossi) in the same area is quite feasible since there are records of four different Melanocetus species in the eastern tropical Pacific (Pietsch & Van Duzer 1980), and M. johnsonii and M. murrayi are commonly taken in the same trawls in the Gulf of Mexico (T. Sutton, pers. comm.).

On the subject of distribution, it should be noted that 52°S was considered as the southern limit of M. johnsonii range to date (Pietsch 2009). Our record significantly extends the species range to the south—23° latitude, or more than 1000 nautical miles—assuming that the toothfish from which our specimen was extracted did not cover this distance after consuming the anglerfish and before being captured. The M. johnsonii specimen was in almost fresh condition and did not show signs of advanced digestion.

Acknowledgements

The authors are grateful to Theodore Pietsch (School of Aquatic and Fishery Sciences, University of Washington, Seattle, USA), Ofer Gon (South African Institute for Aquatic Biodiversity, Grahamstown) and Stewart Hanchet (National Institute of Waters and Atmospheric Research, Nelson, New Zealand) for selected papers provided, Andrew Stewart (Museum of New Zealand Te Papa Tongarewa, Wellington) for information about specimens of M. rossi deposited at the Museum of New Zealand. Special thanks to Theodore Pietsch for reading an early draft and his valuable comments. The authors also appreciate the assistance of Tracey Sutton (Oceanographic Center, Nova Southeastern University, Dania Beach, USA), who improved the English of the manuscript and made some helpful comments.

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