Research Report

First Records of Saddleback Syndrome and Pughead Deformities in the Common Pandora Pagellus erythrinus (Linnaeus, 1758) (Teleostei: Sparidae) from Wild Population in the Northern Aegean Sea, Turkey  

Laith A. Jawad1 , Okan Akyol2 , İlker Aydin2
1 Flat Bush, Manukau, Auckland 2016, New Zealand
2 Ege University Faculty of Fisheries, 35440 Urla, Izmir, Turkey
Author    Correspondence author
International Journal of Marine Science, 2017, Vol. 7, No. 19   doi: 10.5376/ijms.2017.07.0019
Received: 25 Apr., 2017    Accepted: 23 May, 2017    Published: 01 Jun., 2017
© 2017 BioPublisher Publishing Platform
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Preferred citation for this article:

Jawad L.A., Akyol O., and Aydin İ., 2017, First records of saddleback syndrome and pughead deformities in the common pandora Pagellus erythrinus (Linnaeus, 1758) (Teleostei: Sparidae) from wild population in the northern Aegean Sea, Turkey, International Journal of Marine Science, 7(19): 183-187 (doi: 10.5376/ijms.2017.07.0019)

Abstract

The first record of the abnormalities, saddleback syndrome and pughead is reported from common pandora Pagellus erythrinus collected from the northern Aegean Sea, Turkey. Externally, the pughead specimen was with a short neurocranium, normal jaws and mouth was closed. There are a significant osteological damages have been revealed by the radiograph of this deformed specimen. The saddleback anomaly is located in the spinous part of the dorsal fin that showed a loss of 8 spines. In addition, few scales of the lateral line were deformed. The radiograph image showed that the whole 8 spines and their supporting pterygiophores were missing. These abnormalities have been considered as an important indicator of environmentally induced stress to the wild fishes. Hence, the present finding highlights the need for closer monitoring of the marine environment and for the identification of the specific factor that causes these abnormalities.

Keywords
Anomalies; Fin rays; Skull; Vertebral column; Environment

Introduction

Pughead deformity is an abnormal osteological condition that results in the aberration of the maxilla, premaxilla, or infraorbital bones, with variable degrees of severity (Hickey, 1977). Pughead anomaly is an infrequent occurrence in the wild, particularly in large estuarine systems (Berra and Au, 1981). Higher incidences of pughead cases of abnormality were revealed from more polluted waters (Slooff, 1982).

 

The term saddleback syndrome was first proposed by Tave et al. (1983) for an abnormality cases of different degrees of lack of dorsal fin in tilapia Sarotherodon aureus. Since then, this deformity has associated with severe anomaly of the dorsal profile of the fish resulted from deformed dorsal fin pterygiophores. It has been reported from fish species in the wild around the world (Jawad and Al-Mamry, 2012; Diggles, 2013; Boglione et al., 2013; Pollock, 2015).

 

Common pandora is a marine species living in benthopelagic habitat at depth down to 300 m (Bauchot and Hureau, 1986). It distributed in the eastern Atlantic Ocean and the Mediterranean Sea (Sanches, 1991). Individuals of this species prefer deep water during winter time. It is omnivorous, but mainly feed on benthic invertebrates and small fishes. Sex interchange is possible as females become males in their 3rd year of life (Bauchot and Hureau, 1986; Froese and Pauly, 2017).

 

As far as the authors are concerned, the pughead and saddleback syndrome anomalies have not reported for this species previously. Therefore, this report is the first to document the two cases of abnormalities in P. erythrinus and in the Turkish waters.

 

1 Materials and Methods

On 1st July 2016 one specimen of P. erythrinus showing pughead and saddleback syndrome deformities was caught by a bottom trawl (44 mm mesh size in cod-end) at depth of 60 m from Gerence Bay, off Çeşme, Izmir (38°25’N-26°16’E). A normal specimen was also obtained from the same fishing lot used for comparison (Figure 1A; Figure 1B). The specimens were fixed in 70% ethanol and deposited in the fish collection of the Ege University, Fisheries Faculty (ESFM-PIS/2016-10). The skeleton of both normal and abnormal specimens were examined by x-ray and measurements were recorded to the nearest millimetre.

 

 
Figure 1 Pagellus erythrinus; A: normal, 192 mm total length; B: abnormal, 246 mm total length

 

2 Results

2.1 Pughead case

The pug-headed specimen had a 192 mm total length, 153 mm standard length, 18 mm preorbital length, 33 mm postorbital length, 15 mm eye diameter, 47 mm head length and 94 mm predorsal fin length. This specimen is compared to normal fish having 246 mm total length, 202 mm standard length, 21 mm preorbital length, 24 mm postorbital length and 23 and 68 mm head length.

 

Externally, the abnormal specimen was shown to have only short neurocranium with normal jaws and mouth was closed, which means that the deformity has not affected the mechanism of opening and shutting the mouth (Figure 1A; Figure 1B).

 

The osteological deformity was compared with the normal specimen. Internally, the vomer and parasphenoid were shortened, and displacement and/or curvature of the nasals, frontals, vomer, and palatines were observed. Premaxilla is normal and maxilla is reduced in size. Teeth are present, but those located posteriorly on the upper jaw appeared to be deformed in comparison with those of the normal specimen. The forehead is retracted backward and the angle “A 2” between the line passing at the anterior edge of the eye and that passing between the nape and the tip of the mouth is 23°, while that of the normal specimen “A1” is 46°. In comparison with the vertebral column of the normal specimen, the contour of the 1st abdominal vertebra was changed in having concave and convex upper and lower sides respectively and curved and buldging outside anterior and posterior sides respectively (Figure 2A; Figure 2B).

 

 

Figure 2 Radiograph of Pagellus erythrinus; A: normal, 192 mm total length; B: abnormal, 246 mm total length

 

2.2 Saddleback syndrome case

The saddleback is located in the spinous part of the dorsal fin and there are 8 spines missing from the fin. The rays in the soft part look normal. The shape of the saddleback is in a form of a shallow and wide embayment about 2 scale’s lines above the lateral line, with 10 mm depth and 20 mm long. The anterior few scales of the lateral line shown to be deformed otherwise no other anomalies were detected on the fish body. The radiograph image showed that the whole 8 spines and their supporting pterygiophores were missing. The 3 supraneurals were the only bony parts of the dorsal fin were left (Figure 2A; Figure 2B). No other internal skeletal deformities were observed.
 

3 Discussion

Hickey et al. (1977) described 4 stages of pughead deformity in teleostean fishes: normal, primary, secondary and tertiary. The present case of pughead anomaly in P. erythrinus represents the secondary of Hickey et al. (1977) system. Unlike other cases of pughead reported from several fish species (AL-Hassan, 1988; Jawad and Hosie, 2007; Jawad et al., 2014), the present case looks mild as the mouth is closed and the fish can avoid several risks as this closure.

 

Although not much of bone elements were lost from the skull of P. erythrinus, but the deformation in the bones at the anterior part of the cranium could consider this a severe case. The distorted 1st abdominal vertebra shown in the x-ray might have been a result of the displacement of the posterior part of the skull, which in turn has a direct effect on the brain. Since the preorbital area was reduced very much and the nasal openings were affected in this specimen, the nasal organs and probably the olfactory nerve were lost too. Dissection of the skull to study the brain is required to reveal the damages that might occurred to the brain due to the pughead deformity. Similar postcranial skeletal deformity as a result of pughead was reported in the historical case observed by Yiung (1901) on small specimen of salmon species obtained from France.

 

Due to the natural closure of the mouth, the suggestions made by Hickey (1977) in that fishes with pughead deformity may fail the ability to breath and feed, which in turn became unable to compete for obtaining food are not apply to the present specimen. It is also seems that this deformity did not reduced survival potential and the body of the deformed fish is robust inferring the ability to have a quick move when potential predators appear.

 

The causes of the observed pughead anomaly in the specimen examined are unknown, but they probably arise during early development (Cobcroft et al., 2001). The survival rate of abnormal fish, especially during the early ontological stages in the wild, is unknown (Bueno et al., 2015). To determine the overall incidence and effect of these abnormalities, survival throughout development, larva through adult, must be considered.

 

In all cases reporting saddleback syndrome, the dorsal fin in its both parts, spinous and soft, is involved in deformity, where these elements showed missing at different levels (Cobcroft and Battaglene, 2013). In the present specimen, the saddleback is appeared to affect the anterior part, a case which agrees with the results obtained for other fish species (Tave et al., 1983).

 

Both the pughead and saddleback syndrome deformities might resulted from an unhealthy environment, with contaminants originated from anthropogenic activities that has an influence on early life history stages of fish directly (Browder et al., 1993; Gagnon and Rawson, 2009). On the other hand, and for saddleback syndrome, the predation by other fish species and injuries by sea birds on fish specimens in the studied area during early life history remains possible.

 

Future research is required to study the variability of both pughead and saddleback syndrome in both juvenile and adult commercial fish species in different locations and years, taking into consideration the mortalities that related to these two anomalies.

 

Authors’ contributions

All authors have contributed equally toward the publication of this paper.

 

Acknowledgments

We would like to thank the Ege University Faculty of Fisheries, Turkey for giving us the opportunity to examine and study the deformed fish specimens. Our thanks are also due to Sergey Bogorodsky of Station of Naturalists, Omsk, Russia and Ronald Fricke of Staatliches Museum für Naturkunde, Rosenstein, Germany, for identification of the species.

 

References

Al-Hassan L.A.J., 1988, A case of pugheadedness in the croaker Johnius aneus from Khor al-Zubair, northwest of the Arab Gulf, Basrah, Iraq. Indian Journal of Fisheries, 35: 68-69

 

Bauchot M.L., and Hureau J.C., 1986, Sparidae. p. 883-907. In P. J. P. Whitehead, M.-L. Bauchot, J.-C. Hureau, J. Nielsen and E. Tortonese (eds.) Fishes of the north-eastern Atlantic and the Mediterranean. volume 2. UNESCO, Paris

 

Berra T.M., and Au R.J., 1981, Incidence of teratological fishes from Cedar Fork Creek, Ohio. Ohio Journal of Science, 81: 225–229

 

Boglione C., Gisbert E., Gavaia P., Witten P., Moren M., Fontagné S., and Koumoundouros G., 2013, Skeletal anomalies in reared European fish larvae and juveniles. Part 2: main typologies, occurrences and causative factors. Reviews in Aquaculture, 5: S121-S167

https://doi.org/10.1111/raq.12015

https://doi.org/10.1111/raq.12016

 

Browder J., McClellan D., Harper D., and Kandrashoff W., 1993, A major developmental defect observed in several Biscayne Bay, Florida, fish species, Environmental Biology of Fishes, 37: 181-188

https://doi.org/10.1007/BF00000593

 

Bueno L.S., Koenig C.C., and Hostim-Silva M., 2015, First records of ‘pughead’ and ‘short-tail’ skeletal deformities in the Atlantic goliath grouper, Epinephelus itajara (Perciformes: Epinephelidae). Marine Biodiversity Records, 8, p.e72

https://doi.org/10.1017/S1755267215000421

 

Cobcroft J.M., Pankhursta P.M., Sadler J., and Hart P.R., 2001, Jaw development and malformation in cultured striped trumpeter, Latris lineata. Aquaculture, 199: 267–282

https://doi.org/10.1016/S0044-8486(01)00592-0

 

Diggles B.K., 2013, Saddleback deformities in yellowfin bream Acanthopagrus australis (Günther) from South-East Queensland. Journal of Fish Diseases, 36: 521–527

https://doi.org/10.1111/jfd.12021

PMid:23121304

 

Froese R., and Pauly D., (eds) 2017, FishBase. World Wide Web electronic publication. www. fishbase.org, version (01/2017)

 

Hickey C.R., Young B.H., and Bishop R.D., 1977, Skeletal abnormalities in Striped Bass. New York Fish and Game Journal, 24: 69–85

 

James P.S.B.R., and Badrudeen M., 1968, On certain anomalies in the fishes of the family Leiognathidae. Journal of the Marine Biological Association of India, 10: 107–113

 

Jawad L., and Hosie A., 2007, On the record of pug-headedness in snapper, Pagrus auratus (Forster, 1801)(Perciformes, Sparidae) from New Zealand, Acta Adriatica, 48: 205-210

 

Jawad L.A., Kousha A., Sambraus F., and Fjelldal P.G., 2014, On the record of pug-headedness in cultured Atlantic salmon, Salmo salar Linnaeus, 1758 (Salmoniformes, Salmonidae) from Norway, Journal of Applied Ichthyology, 30: 537-539

https://doi.org/10.1111/jai.12403

 

Pollock B.R., 2015, Saddleback syndrome in yellowfin bream (Acanthopagrus australis (Günther, 1859)) in Moreton Bay, Australia: its form, occurrence, association with other abnormalities and cause, Journal of Applied Ichthyology, 31: 487-493

https://doi.org/10.1111/jai.12437

 

Sanches J.G., 1991, Catálogo dos principais peixes marinhos da República de Guiné-Bissau, Publ. Avuls. Inst. Nac. Invest. Pescas, 16: 429

 

Shariff M., Zainuddin A.T., and Abdullah H., 1986, Pugheadedness in Bighead Carp, Aristichthys nobilis (Richardson), Journal of Fish Disease, 9: 457–460

https://doi.org/10.1111/j.1365-2761.1986.tb01039.x

 

Slooff W., 1982, Skeletal anomalies in fish from polluted surface waters. Aquatic Toxicology, 2: 157–173

https://doi.org/10.1016/0166-445X(82)90013-3

 

Tave D., Bartels J.E., and Smitherman R.O., 1983, Saddleback: a dominant, lethal gene in Sarotherodon aureus (Steindachner) (= Tilapia aurea). Journal of Fish Diseases, 6: 59-73

https://doi.org/10.1111/j.1365-2761.1983.tb00051.x

 

Yiung E., 1901, Note sur un Cas de Monstruosit 6 de la TMte chez une Truite. Revue Suisse Zoologie, 9: 307-313

https://doi.org/10.5962/bhl.part.75161
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