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Article

The Indo-Pacific Sergeant Abudefduf vaigiensis (Quoy & Gaimard, 1825) (Perciformes: Pomacentridae) in Libya, South-Central Mediterranean Sea

by
David Osca
1,
Valentina Tanduo
1,
Francesco Tiralongo
2,3,
Ioannis Giovos
4,
Sara A. A. Almabruk
5,
Fabio Crocetta
1,* and
Jamila Rizgalla
6
1
Department of Integrative Marine Ecology, Stazione Zoologica Anton Dohrn, Villa Comunale, I-80121 Napoli, Italy
2
Ente Fauna Marina Mediterranean, Scientific Organization for Research and Conservation of Marine Biodiversity, I-96012 Avola, Italy
3
Department of Biological, Geological and Environmental Science, University of Catania, I-95131 Catania, Italy
4
iSea, Environmental Organization for the Preservation of the Aquatic Ecosystems, GR-55438 Thessaloniki, Greece
5
Zoology Department, Faculty of Science, Omar Al-Mokhtar University, P.O. Box 919 El Bayda, Libya
6
Department of Aquaculture, Faculty of Agriculture, University of Tripoli, P.O. Box 13275 Tripoli, Libya
*
Author to whom correspondence should be addressed.
J. Mar. Sci. Eng. 2020, 8(1), 14; https://doi.org/10.3390/jmse8010014
Submission received: 29 November 2019 / Revised: 20 December 2019 / Accepted: 21 December 2019 / Published: 24 December 2019
(This article belongs to the Special Issue Marine Biodiversity in the Anthropocene)
Browse Figures
Versions Notes

Abstract

:
The Indo-Pacific Sergeant Abudefduf vaigiensis (Quoy & Gaimard, 1825) (Chordata: Pisces: Actinopterygii: Perciformes: Pomacentridae) is first recorded in the south-central Mediterranean Sea (Libya), based on the external morphology and the barcoding of a fragment of the cytochrome c oxidase subunit I gene. Present sightings from field surveys and social media include juveniles, sub-adults, and a single adult specimen, suggesting that the species is now established in Libyan waters. No certainties occur regarding timing and possible pathway of arrival of this species in the area, and it may have simply gone undetected for years. The joint effort of field studies and citizen science projects in collaboration with international organizations continues shedding light on bioinvasions in Libya, with valuable outcomes for the Mediterranean marine biology as a whole.

1. Introduction

Biological pollution is a common phenomenon worldwide. Although marine invasions have been widely documented all over the world [1], they are very relevant in the Mediterranean Sea, where native species are often even outnumbered by congeneric or confamilial taxa [2]. The family Pomacentridae Bonaparte, 1831 in the Mediterranean Sea, as an example, includes a single native species, Chromis chromis (Linnaeus, 1758), and seven additional alien or cryptogenic taxa, namely Abudefduf hoefleri (Steindachner, 1881), Abudefduf saxatilis (Linnaeus, 1758), Abudefduf sexfasciatus (Lacepède, 1801), Abudefduf vaigiensis (Quoy & Gaimard, 1825), Chrysiptera cyanea (Quoy & Gaimard, 1825), Chrysiptera hemicyanea (Weber, 1913), and Stegastes variabilis (Castelnau, 1855) (Table 1, Figure 1).
The majority of these species are known from the Mediterranean basin based on single records, some of which were obtained through social media and citizen scientist projects [4,9]. However, the Sergeant-major (A. saxatilis) and the Indo-Pacific Sergeant (A. vaigiensis) were recorded from larger parts of the Mediterranean Sea for decades, with A. vaigiensis being first recorded in Italy more than 60 years ago [4,5,6,7,10,11,12,13]. In addition, despite putative distinct colour-pattern features should allow their easy visual identification (according to the literature, in A. saxatilis the fifth vertical dark bar extends without gap on the posterior margin of the dorsal fin, whereas in A. vaigiensis it has a gap between it and the dorsal fin; in A. saxatilis, two black spots are present on the caudal peduncle, whereas they are absent in A. vaigiensis [6,7,17,18]), the local distribution and state of these two species still remain ambiguous due to misidentifications between the two congeners, with some researchers even doubting the presence of consistent meristic or morphometric differences (Gerald R. Allen, Western Australian Museum, Perth, Australia; pers. comm. [5]). In this light, recent confirmed records from the Mediterranean Sea only relied on barcoding of selected specimens [6,7,13].
The introduction pathway in the Mediterranean Sea of both A. saxatilis and A. vaigiensis also remains unclear, an uncertainty which is partly due to the patchy distribution with long distances between the observation points (Table 1 and Figure 1). Several pathways were proposed for A. saxatilis, including aquarium release, ship transport, or even natural range expansion through the Gibraltar Strait [4,5,19], and the same holds for A. vaigiensis, whose proposed pathways included aquarium release, ship transport, or Lessepsian invasion through the Suez Canal [11,13,19,20,21].
The aim of the present paper is to first report the presence of A. vaigiensis in south-central Mediterranean Sea (Libya) based on external morphology and barcoding of a fragment of the cytochrome c oxidase subunit I (COI) gene. In addition, we here highlight the additional observation of an Abudefduf specimen matching the morphological characters of A. saxatilis, thus suggesting that also the occurrence of A. saxatilis in Libya may be possible.

2. Materials and Methods

The data reported in the present paper fall within the framework of an ongoing project that aims at monitoring the marine biodiversity in Libya by integrating information gained from field surveys and social media (citizen science projects and mining Facebook™ posts).
Field surveys were conducted in two stages, from 14th June to 7th November 2018 and from 5th May to 29th October 2019, in an area of approximately 90 hectares with a 2.2 km long coastline in a natural shallow water bay, situated 12 km west of Tripoli Harbour and known as “Regatta” or “Magribi Arabic Touristic Village”. Along this coastline, there is a shallow water natural bay (32.8539° N, 13.0543° E) formed between two islands subjected to tidal movements. The natural bay consists of sandy and rocky substrates. Snorkel surveys were undertaken, weather permitting, at several locations within the bay and along the island margins, and consisted of a consecutive series of 2–6-h-long snorkel dives up to 2 m depth. Pictures and short pieces of footage were taken in situ using Tough TG-3 and TG-4 Olympus underwater cameras. A single Abudefduf specimen was taken with the help of a hand net, and then placed in 90–96% ethanol for preservation and further study.
Six Facebook™ groups with an interest in both recreational and professional fishing were monitored daily for recent postings from January 2018 to September 2019. Furthermore, relevant posts prior to these dates and extending back to 2012 were also screened. Owners of relevant posts were contacted to obtain information on posted material, and permission was sought from the owners of the Facebook™ post.
Genomic DNA of the single Abudefduf specimen sampled was extracted from the caudal fin by using the NucleoSpin® Tissue (Macherey-Nagel) kit, following the manufacturer’s protocol. Partial sequence of the COI gene was amplified using the primers developed by Baldwin et al. [22]: forward - FISH-BCL: 5′-TCAACYAATCAYAAAGATATYGGCAC-3′; reverse - FISH-BCH: 5′-TAAACTTCAGGGTGACCAAAAAATCA-3′. The polymerase chain reaction (PCR) was conducted in 25 μL volume reaction, containing 2.5 μL of Roche buffer (10×), 2.5 μL (2 mM) of dNTPack Mixture (Roche), 2 μL each of forward and reverse primers, 0.25 μL (5 U/μL) of Roche Taq DNA polymerase, 1 μL of DNA (15 ng/μL) and sterilized distilled water up to 25 μL. Amplification was performed with an initial denaturation for 5 min at 95 °C, followed by 39 cycles of 1 min at 95 °C, 1 min annealing at 47 °C and 1 min at 72 °C, with a final extension of 5 min at 72 °C. The successful PCR product was purified and Sanger sequenced through an automated DNA sequencer (ABI PRISM 3730) at the Molecular Biology and Sequencing Service of SZN (Naples, Italy). Forward and reverse sequences obtained were assembled using Sequencher v. 5.0.1 (GeneCodes Co.) and compared with reference sequences from the entire NCBI nucleotide (NT) database using BLASTn [23] as to confirm the morphological identification and further verify the diagnostic nucleotide positions reported by Tsadok et al. [6].

3. Results

The field surveys held in Regatta yielded 6 different records, for a total of 9 specimens belonging to the genus Abudefduf (Table 2, Figure 2). However, some of these records may be based on the same individuals; in fact, from a cautious point of view, the records reported comprise at least 4 different specimens. The majority of the sightings (6) regarded specimens with an oval-shaped body, silvery-white belly in color with a yellow part around the base of the dorsal fin and five vertical conspicuous black bars, four on the trunk and the fifth located on the caudal peduncle, thus coinciding with morphological characters of A. vaigiensis. Among specimens showing such characters, a single juvenile individual (TL ~2.2 cm) was sampled on the 25th August 2019. All remaining individuals were only photographed, and these comprise at least a pair of larger individuals (TL ~5 cm) observed on the 18th September 2019. On the other hand, among the observed fishes, an individual showing morphological traits characteristic of A. saxatilis (and in particular two black spots on the caudal peduncle) was seen in three different days during October 2019 (Table 2, Figure 2).
Mining of Facebook™ posts backdated the presence of the genus Abudefduf in Libya to as early as the 10th July 2018, when a single adult specimen (TL ~10 cm) of A. vaigiensis was sampled at shallow depths in Janzur, a locality 5 km west of Regatta, by a professional fisherman with a trammel net (Table 2, Figure 2).
A 663 bp partial sequence of the COI gene was obtained. BLASTn queries generated sequences with a 100% identical score to A. vaigiensis, although high similarities (until 99.85%) were also obtained with A. sexfasciatus. Our analysis on the diagnostic nucleotide positions revealed: i) two sequences identical to our (AP006016 with an unknown sampling locality, and MF123716 from the Gulf of Aqaba, Red Sea) [24,25]; ii) four sequences (MF123711, MF123713, MF123717, KF186627) from the Gulf of Aqaba and generally the Red Sea with a difference in position 346 [6,25]; iii) one sequence (FJ237571) from India with a difference in position 2 [26]; iv) two sequences (MF123715 and MF123714) from the Gulf of Aqaba with differences in positions 328 and 346 [25]; and v) one sequence (MF123712) from the Gulf of Aqaba with six differences in positions 58, 81, 105, 322, 346, and 484 [25].

4. Discussion

Molecular results obtained here are in agreement with data reported by Bertrand et al. [27], who noticed that an A. vaigiensis lineage was found to be nested within A. sexfasciatus in the mitochondrial gene tree, whereas both species were only found to be distinct based on nuclear information. Alternatively, another possibility is that some misidentifications may be at the basis of the sequences deposited in GenBank. However, A. vaigiensis and A. sexfasciatus clearly differ with regards morphology and color pattern, which definitively excludes A. sexfasciatus and confirms that the sequenced specimen from Libya belongs to A. vaigiensis. In addition, the 25 diagnostic positions reported by Tsadok et al. [6] to differentiate between A. vaigiensis and A. saxatilis are lowered here to 22 due to the presence of three A. saxatilis diagnostic nucleotide positions (105, 322, and 484) in the MF123712 sequence of A. vaigiensis.
To date, records of A. vaigiensis and of A. saxatilis were still unknown from the Mediterranean coastline of Africa, despite A. vaigiensis being first found in the central Mediterranean more than half a century ago [10], whereas A. saxatilis has become a commonly encountered taxon along the easternmost coastline of the Mediterranean Sea [6]. The present record of A. vaigiensis therefore fills a gap in the distribution of this taxon in the newly invaded area, and suggests that the species is now established in Libyan waters. With respect to its congeneric species A. saxatilis, records based only on morphology were published in Spain [4] and Malta [5,7]. If these records are true, then the sighting of an Atlantic species in the easternmost Mediterranean Sea [6] could be due to the presence of populations even in the western and central Mediterranean. In this light, its potential occurrence in Libya may also be possible; however, further field work and molecular analysis is needed to confirm that.
The new records reported here immediately raise the question of the origin of these specimens. Indeed, the most plausible hypothesis is that these fishes may have recently spread from nearby detected or yet-undetected populations. However, another plausible hypothesis is also that these and additional central Mediterranean populations may have simply gone undetected since years. In this light, the finding of a larger individual showing morphological features associated with reproductive activity, as well as the discovery of juveniles in two consecutive years, also strongly suggests the presence of this fish in the area well before the dates recorded here, and the possible presence of an undetected population in the area. Alternatively, these specimens may have been locally introduced through ship transport, and the findings in Janzur and Regatta may be the result of different intrusion attempts.
Alien invasion in the Mediterranean Sea is an increasing phenomenon, with reports of fishes held from various countries in the recent years (e.g., [28,29,30,31,32]). Libya, due to its geographic position, situated in the south-central Mediterranean Sea and possessing a coastline of ~1770 km, would constitute a key country to study the spreading of alien, cryptogenic, and newcomer species from the western Atlantic to the eastern Mediterranean and from the Red Sea to the western Mediterranean. However, it still lacks intensive systematic efforts for monitoring invasive marine species [33], a situation which is amplified by the wide political unrest in the region. Despite that, the number of alien species recorded in recent years is increasing thanks to field surveys, citizen-science projects, and international collaborations [33,34,35,36,37,38,39,40,41,42,43,44]. Therefore, if these joint efforts continue, the outcomes obtained will be valuable and useful for the Mediterranean marine biology as a whole.

Author Contributions

Conceptualization, D.O., F.C. and J.R.; methodology, D.O., F.C. and J.R.; lab work, D.O. and V.T.; field work, J.R.; bibliographic researches, D.O., V.T., F.T. and I.G.; social media data mining, J.R. and S.A.A.A.; writing—original draft preparation, D.O., F.C. and J.R.; writing—review and editing, D.O., V.T., F.T., I.G., S.A.A.A., F.C. and J.R.; funding acquisition, F.C. and J.R. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Acknowledgments

The fisherman Rabee Ahmad Sulatan provided information on the record in Janzur and allowed publication of the photo. The administration of Regatta granted free pass to conduct field surveys in 2019 and the security personnel provided a safe environment. Fedai provided assistance and an anonymous child helped catching the fish. Leticia Latanzy transported the Abudefduf specimen to Italy. We are grateful to all of them.

Conflicts of Interest

The authors declare no conflict of interest.

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Jmse 08 00014 g001 550
Figure 1. Sightings of alien and cryptogenic taxa belonging to the family Pomacentridae Bonaparte, 1831 from the Mediterranean Sea. Numbers refer to literature records (see also Table 1). Black pentagon refers to present record.
Figure 1. Sightings of alien and cryptogenic taxa belonging to the family Pomacentridae Bonaparte, 1831 from the Mediterranean Sea. Numbers refer to literature records (see also Table 1). Black pentagon refers to present record.
Jmse 08 00014 g001
Jmse 08 00014 g002 550
Figure 2. Specimens belonging to the genus Abudefduf Forsskål, 1775 reported in the present study from Libya. (A–F) Abudefduf vaigiensis. (G,H). Abudefduf cf. saxatilis. White arrows highlighting the two black spots on the caudal peduncle.
Figure 2. Specimens belonging to the genus Abudefduf Forsskål, 1775 reported in the present study from Libya. (A–F) Abudefduf vaigiensis. (G,H). Abudefduf cf. saxatilis. White arrows highlighting the two black spots on the caudal peduncle.
Jmse 08 00014 g002
Table
Table 1. Records of alien and cryptogenic taxa belonging to the family Pomacentridae Bonaparte, 1831 from the Mediterranean Sea, with origin, country and locality with coordinates, year of first sighting, number of specimens (N), environment, method of observation, and references (R) as listed in literature (see also Figure 1). Abbreviations used: AO—Eastern and Western Atlantic Ocean; EA—Eastern Atlantic; IP—Indo-Pacific; IWP—Indo-West Pacific; WA—Western Atlantic.
Table 1. Records of alien and cryptogenic taxa belonging to the family Pomacentridae Bonaparte, 1831 from the Mediterranean Sea, with origin, country and locality with coordinates, year of first sighting, number of specimens (N), environment, method of observation, and references (R) as listed in literature (see also Figure 1). Abbreviations used: AO—Eastern and Western Atlantic Ocean; EA—Eastern Atlantic; IP—Indo-Pacific; IWP—Indo-West Pacific; WA—Western Atlantic.
TaxonOriginCountry and LocalityYearNEnvironmentMethodR
Abudefduf hoefleri
(Steindachner, 1881)		EAMalta, Delimara
35.8352° N, 14.5626° E		20141shallow coastal waterssampled[3]
Abudefduf saxatilis
(Linnaeus, 1758)		AOSpain, Tarragona
41.1310° N, 1.3704° E		200912 mobserved[4]
Malta, Valletta Grand Harbour
35.5337° N, 14.3052° E		20136-7close to the cruise-ship passenger terminalobserved[5]
Israel, Sdot-Yam
32.2932° N, 34.5315° E		201310shallow rocky reef
1.5–2 m		sampled[6]
Malta, Valletta Grand Harbour
35.8982° N, 14.5206° E		2013–20143-observed[7]
Turkey, Çandarlı Bay
38.5144° N, 26.5251° E		201611–3 mobserved[8]
Abudefduf sexfasciatus
(Lacepède, 1801)		IPGreece, Sounio
37.6773° N, 24.0554° E		201712 mobserved[9]
Abudefduf vaigiensis
(Quoy & Gaimard, 1825)		IPItaly, Gulf of Naples
40.4754° N, 14.1230° E		19571100 m from seashoresampled[10]
Israel, Rosh Ha’Nikra
33.0885° N, 35.1053° E		19971littoral platform
1–2 m		sampled[11]
Italy, Gulf of Genoa
44.1510° N, 9.2541° E		19981vertical rocky wall
2 m		observed[12]
Malta, Valletta Grand Harbour
35.8982° N, 14.5206° E		20132-sampled[7]
Malta, Valletta Grand Harbour and nearby
35.9029° N, 14.5205° E		20156-sampled[7]
Lebanon
~34.0085° N, 35.0211° E		≤20151-sampled[13]
Chrysiptera cyanea
(Quoy & Gaimard, 1825)		IWPSlovenia, Portoroz
45.3048° N, 13.3459° E		20131salt storehouseobserved[14]
Chrysiptera hemicyanea
(Weber, 1913)		IWPMalta, Marsaxmett Harbour
35.5445° N, 14.3011° E		20171large rocks and boulders
2 m		observed[15]
Stegastes variabilis
(Castelnau, 1855)		WAMalta, Senglea
35.8910° N, 14.5142° E		20131waterfront
2 m		sampled[16]
Table
Table 2. Records of specimens belonging to the genus Abudefduf Forsskål, 1775 from Libya, with locality, coordinates, date, method of observation, morphological identification, number of specimens (N), GenBank accession number, and figures (see Figure 2).
Table 2. Records of specimens belonging to the genus Abudefduf Forsskål, 1775 from Libya, with locality, coordinates, date, method of observation, morphological identification, number of specimens (N), GenBank accession number, and figures (see Figure 2).
LocalityCoordinatesDateMethodMorphological IdentificationNGenBankFigure
Janzur32.5028° N, 13.0106° E10.07.2018FacebookA. vaigiensis1-Figure 2A
Regatta32.8539° N, 13.0543° E7.09.2018field surveyA. vaigiensis1-Figure 2B
Regatta32.8539° N, 13.0543° E25.08.2019field surveyA. vaigiensis1MN852855Figure 2C–D
Regatta32.8539° N, 13.0543° E18.09.2019field surveyA. vaigiensis2-Figure 2E–F
Regatta32.8539° N, 13.0543° E1.10.2019field surveyA. cf. saxatilis1-Figure 2G
Regatta32.8539° N, 13.0543° E19.10.2019field surveyA. cf. saxatilis and A. vaigiensis2--
Regatta32.8539° N, 13.0543° E29.10.2019field surveyA. cf. saxatilis and A. vaigiensis2-Figure 2H

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MDPI and ACS Style

Osca, D.; Tanduo, V.; Tiralongo, F.; Giovos, I.; Almabruk, S.A.A.; Crocetta, F.; Rizgalla, J. The Indo-Pacific Sergeant Abudefduf vaigiensis (Quoy & Gaimard, 1825) (Perciformes: Pomacentridae) in Libya, South-Central Mediterranean Sea. J. Mar. Sci. Eng. 2020, 8, 14. https://doi.org/10.3390/jmse8010014

AMA Style

Osca D, Tanduo V, Tiralongo F, Giovos I, Almabruk SAA, Crocetta F, Rizgalla J. The Indo-Pacific Sergeant Abudefduf vaigiensis (Quoy & Gaimard, 1825) (Perciformes: Pomacentridae) in Libya, South-Central Mediterranean Sea. Journal of Marine Science and Engineering. 2020; 8(1):14. https://doi.org/10.3390/jmse8010014

Chicago/Turabian Style

Osca, David, Valentina Tanduo, Francesco Tiralongo, Ioannis Giovos, Sara A. A. Almabruk, Fabio Crocetta, and Jamila Rizgalla. 2020. "The Indo-Pacific Sergeant Abudefduf vaigiensis (Quoy & Gaimard, 1825) (Perciformes: Pomacentridae) in Libya, South-Central Mediterranean Sea" Journal of Marine Science and Engineering 8, no. 1: 14. https://doi.org/10.3390/jmse8010014

APA Style

Osca, D., Tanduo, V., Tiralongo, F., Giovos, I., Almabruk, S. A. A., Crocetta, F., & Rizgalla, J. (2020). The Indo-Pacific Sergeant Abudefduf vaigiensis (Quoy & Gaimard, 1825) (Perciformes: Pomacentridae) in Libya, South-Central Mediterranean Sea. Journal of Marine Science and Engineering, 8(1), 14. https://doi.org/10.3390/jmse8010014

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