ANTİCOAGULANT AND ANTİLİPAEMİC ACTİVİTİES OF POLYSACCHARİDES FROM MARİNE ALGAE

Anticoagulant and antilipaemic activities of polysaccharides from marine algae

Kasım Cemal Güven, Burak Coban, Ekrem Sezik

Turkish Marine Research Foundation (TUDAV), PK 10, Beykoz, Istanbul, TURKEY
Department of Chemistry, Bulent Ecevit University, Incivez, 67100 Zonguldak, TURKEY
Institute of Health Sciences, Yeditepe University, 34755, Istanbul, TURKEY

Abstract

In this review the research on the anticoagulant and antilipaemic activity of sulfated and synthetically modified polysaccharides extracted from marine macro algae between 1913 and 2018 was summarized and the results were compared with a long known natural polysaccharide from animal sources, heparin which contain N-sulfate group. The highest anticoagulant activity of algal sulfated polysaccharide was obtained from Dictiyota menstrualis, red alga, found to be 4.8 times more active than heparin. Antilipaemic activity of some algal sulfated polysaccharides showed similar activity as heparin.

Keywords: Anticoagulant, antilipaemic, polysaccharides

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References

Abdel-Fattah, A.F., Hussein, M.M.-E., Salem, H.M. (1973) Sargassan: A sulphated heteropolysaccharide from Sargassum linifolium. Phytochem 12(8): 1995-1998.

Abdel-Fattah, A.F., Hussein, M.M.-D., Salem, H.M. (1974) Studies of the purification and some properties of sargassan, a sulphated heteropolysaccharide from Sargassum linifolium. Carbohydr Res 33(1): 9-17.

Abou-Zeid, A.H., Aboutabl, E.A., Sleem, A.A., El-Rafie, H.M. (2014) Water soluble polysaccharides extracted from Pterocladia capillacea and Dictyopteris membranacea and their biological activities. Carbohydr Polym 113: 62-66.

Adams, S.S., Heathcote, B.V., Walker, D. (1962) Sulphated degraded laminarin: an antilipaemic agent. J Atheroscler Res 2: 314-316.

Adams, S.S., Thorpe, H.M. (1957) The anticoagulant activity and toxicity of laminarine sulphate K. J Pharm Pharmacol 9(1): 459-463.

Aktin, E., Güven, K.C. (1965) Studies on antilipemic properties of the algae collected from Turkish coasts – III. Sargassum vulgare Ag., Polysiphonia subulifera (C. Agardh) Harvey. Qual Plant Mater Veget 12(2): 210-215.

Aktin, E., Güven, K.C. (1969) Studies on the lipase released by the substances obtained from Gracilaria verrucosa (Hunds.) and Gelidium latifolium (Greville). Arzneimittel-Forsch 19(2): 190-193.

Alban, S., Kraus, J., Franz, G. (1992) Synthesis of laminarin sulfates with anticoagulant activity. Arzneimittel-Forsch 42(8): 1005-1008.

Albuquerque, I.R., Queiroz, K.C., Alves, L.G., Santos, E.A., Leite, E.L., Rocha, H.A. (2004) Heterofucans from Dictyota menstrualis have anticoagulant activity. Braz J Med Biol Res 37(2): 167-171.

Almeida-Lima, J., Costa, L.S., Silva, N.B., Melo-Silveira, R.F., Silva, F.V., Felipe, M.B., Medeiros, S.R., Leite, E.L., Rocha, H.A. (2010) Evaluating the possible genotoxic, mutagenic and tumor cell proliferation-inhibition effects of a non-anticoagulant, but antithrombotic algal heterofucan. J Appl Toxicol 30(7): 708-715.

Almeida-Lima, J., Dantas-Santos, N.L., Gomes, D., Cordeiro, S.L., Sabry, D.A., Costa, L.S., Freitas, M.D.L., Silva, N.B., Moura, C.E.B., Lemos, T.M.A.M., Leite, E.L., Rocha, H.A.O. (2011) Evaluation of acute and subchronic toxicity of a non-anticoagulant, but antithrombotic algal heterofucan from the Spatoglossum schröederi in Wistar rats. Rev Bras Farmacogn 21: 674-679.

Anderson, W., Duncan, J.G.C., Harthill, J. E. (1965) The anticoagulant activity of carrageenan. J Pharm Pharmacol 17(10): 647-654.

Arenajo, A.R., Ybanez, A.P., Ababan, M.M.P., Villajuan, C. E., Lasam, M.R.M., Young, C.P., Reyes, J.L.A. (2017) The potential anticoagulant property of Caulerpa lentillifera crude extract. Int J Health Sci 11(3): 29-32.

Astrup, T., Mullertz, S. (1952) The fibrin plate method for estimating fibrinolytic activity. Arch Biochem Biophys 40(2): 346-351.

Athukorala, Y., Jung, W.-K., Vasanthan, T., Jeon, Y.-J. (2006) An anticoagulative polysaccharide from an enzymatic hydrolysate of Ecklonia cava. Carbohydr Polym 66(2): 184-191.

Athukorala, Y., Lee, K., Kim, S., Jeon, Y. (2007) Anticoagulant activity of marine green and brown algae collected from Jeju Island in Korea. Bioresour Technol 98(9): 1711-1716.

Baker, S.P. (1957) Heparin-activated clearing factor; standardized test, agewise application, and clinical observations. Circulation 15(6): 889-896.

Ben Gara, A., Ben Abdallah Kolsi, R., Chaaben, R., Hammami, N., Kammoun, M., Paolo Patti, F., El Feki, A., Fki, L., Belghith, H., Belghith, K. (2017) Inhibition of key digestive enzymes related to hyperlipidemia and protection of liver-kidney functions by Cystoseira crinita sulphated polysaccharide in highfat diet-fed rats. Biomed Pharmacother 85: 517-526.

Bergström, S. (1935) Über die wirkungsgruppe des heparins. Naturwissenschaften 23(41): 706-706.

Bergström, S. (1936) Über polysaccharides terschwefelsäuren mit heparin wirkung. H-S Z Physiol Chem 238(4-5): 163-168.

Bernardi, G., Springer, G.F. (1962) Properties of highly purified fucan. J Biol Chem 237: 75-80.

Besterman, E.M.M., Evans, J. (1957) Antilipaemic agent without anticoagulant action. Brit Med J 1: 310-312.

Bilan, M.I., Klochkova, N.G., Ustyuzhanina, N.E., Chizhov, A.O., Shashkov, A.S., Nifantiev, N.E., Usov, A.I. (2016) Polysaccharides of algae 68. Sulfated polysaccharides from the Kamchatka brown alga Laminaria bongardiana. Russ Chem Bull 65(11): 2729-2736.

Camara, R.B.G., Costa, L.S., Fidelis, G.P., Nobre, L.T.D.B., Dantas-Santos, N., Cordeiro, S.L., Costa, M.S.S.P., Alves, L.G., Rocha, H.A.O. (2011) Heterofucans from the brown seaweed Canistrocarpus cervicornis with anticoagulant and antioxidant activities. Mar Drugs 9(1): 124.

Cao, J., Wang, S.C., Yao, C.W., Xu, Z., Xu, X.M. (2016) Hypolipidemic effect of porphyran extracted from Pyropia yezoensis in ICR mice with high fatty diet. J Appl Phycol 28: 1315-1322.

Carlucci, M.J., Pujol, C.A., Ciancia, M., Noseda, M.D., Matulewicz, M.C., Damonte, E.B., Cerezo, A.S. (1997) Antiherpetic and anticoagulant properties of carrageenans from the red seaweed Gigartina skottsbergii and their cyclized derivatives: correlation between structure and biological activity. Int J Biol Macromol 20(2): 97-105.

Chandía, N.P., Matsuhiro, B. (2008) Characterization of a fucoidan from Lessonia vadosa (Phaeophyta) and its anticoagulant and elicitor properties. Int J Biol Macromol 42(3): 235-240.

Chargaff, E., Bancroft, F.W., Brown, M.S. (1936) Studies on the chemistry of blood coagulation: II. On the inhibition of blood clotting by substances of high molecular weight. J Biol Chem 115: 155-161.

Chen, X., Yang, S., Wang, J., Song, L., Xing, R., Liu, S., Yu, H., Li, P. (2015) Sulfated polysaccharides isolated from cloned Grateloupia filicina and their anticoagulant activity. BioMed Res Int. doi: 10.1155/2015/612352.

Cheng, Z., Wang, S. (2003) Study on anticoagulant activities in vitro of fucoidan and fucoidan / collagen blends. J Funct Polym 2003(4): 557-560.

Chevolot, L., Foucault, A., Chaubet, F., Kervarec, N., Sinquin, C., Fisher, A.M., Boisson-Vidal, C. (1999) Further data on the structure of brown seaweed fucans: relationships with anticoagulant activity. Carbohydr Res 319(1-4): 154-165.

Chevolot, L., Mulloy, B., Ratiskol, J., Foucault, A., Colliec-Jouault, S. (2001) A disaccharide repeat unit is the major structure in fucoidans from two species of brown algae. Carbohydr Res 330(4): 529-535.

Ciancia, M., Quintana, I., Vizcarguenaga, M.I., Kasulin, L., DeDios, A., Estevez, J.M., Cerezo, A.S. (2007) Polysaccharides from the green seaweeds Codium fragile and C. vermilara with controversial effects on hemostasis. Int J Biol Macromol 41(5): 641-649.

Colliec, S., Fischer, A.M., Tapon-Bretaudiere, J., Boisson, C., Durand, P., Jozefonvicz, J. (1991) Anticoagulant properties of a fucoidan fraction. Thromb Res 64(2): 143-154.

Colliec-Jouault, S., Millet, J., Helley, D., Sinquin, C., Fischer, A.M. (2003) Effect of low-molecular-weight fucoidan on experimental arterial thrombosis in the rabbit and rat. J Thromb Haemost 1(5): 1114-1115.

Constantinides, P., Cairns, A., Werner, A. (1954) Antilipemic activity of sulfated polysaccharides. Arch Int Pharmacodyn Ther 99(3-4): 334-345.

Constantinides, P., Johnson, C., Fahrni, B.M., Nakashima, R., Mc, I.H. (1960) Human hyperlipaemia and hypercholesterolaemia: rapid correction with a sulphated polymannuronide. Brit Med J 1(5172): 535-540.

Costa, L.S., Fidelis, G.P., Cordeiro, S.L., Oliveira, R.M., Sabry, D.A., Camara, R.B., Nobre, L.T., Costa, M.S., Almeida-Lima, J., Farias, E.H., Leite, E.L., Rocha, H.A. (2010) Biological activities of sulfated polysaccharides from tropical seaweeds. Biomed Pharmacother 64(1): 21-28.

Cumashi, A., Ushakova, N.A., Preobrazhenskaya, M.E., D’Incecco, A., Piccoli, A., Totani, L., Tinari, N., Morozevich, G.E., Berman, A.E., Bilan, M.I., Usov, A.I., Ustyuzhanina, N.E., Grachev, A.A., Sanderson, C.J., Kelly, M., Rabinovich, G.A., Iacobelli, S., Nifantiev, N.E. (2007) A comparative study of the anti-inflammatory, anticoagulant, antiangiogenic, and antiadhesive activities of nine different fucoidans from brown seaweeds. Glycobiology 17(5): 541-552.

de Lara-Isassi, G., Alvarez-Hernandez, S., Quintana-Pimentel, A. (2004) Screening for anticoagulant substances in some marine macroalgae. Hydrobiologia 14(1): 47-54.

de Zoysa, M., Nikapitiya, C., Jeon, Y.-J., Jee, Y., Lee, J. (2008) Anticoagulant activity of sulfated polysaccharide isolated from fermented brown seaweed Sargassum fulvellum. J Appl Phycol 20(1): 67-74.

Deacon-Smith, R.A., Lee-Potter, J.P., Rogers, D.J. (1985a) Anticoagulant activity in extracts of British marine algae. Bot Mar 28(8): 333.

Deacon-Smith, R.A., Lee-Potter, J.P., Rogers, D.J. (1985b) Platelet aggregation in the presence of extracts of British marine algae. Med Lab Sci 42(4): 404-405.

Deacon-Smith, R.A., Rogers, D.J. (1982) Antihaemostatic activities of British marine algae. Brit Phycol J 17: 231.

Demole, V., Reinert, M. (1930) Polyanetholsulfosaures Natrium, ein neues synthetisches Mittel zur Hemmung der Blutgerinnung. N-S Arch Exp Pathol Pharmakol 158(1): 211-218.

Dewar, E.T. (1956) Sodium laminarin sulphate as a blood anticoagulant. Paper read at 2nd Int. Seaweed Symposium, Trondheim.

Dobashi, K., Nishino, T., Fujihara, M., Nagumo, T. (1989) Isolation and preliminary characterization of fucose-containing sulfated polysaccharides with blood-anticoagulant activity from the brown seaweed Hizikia fusiforme. Carbohydr Res 194: 315-320.

Doctor, V.M., Lewis, D., Coleman, M., Kemp, M.T., Marbley, E., Sauls, V. (1991) Anticoagulant properties of semisynthetic polysaccharide sulfates. Thromb Res 64(4): 413-425.

Dodgson, K., Price, R. (1962) A note on the determination of the ester sulphate content of sulphated polysaccharides. Biochem J 84(1): 106-110.

Dore, C.M.P.G., Faustino Alves, M.G.D.C., Pofírio Will, L.S.E., Costa, T.G., Sabry, D.A., de Souza-Rêgo, L.A.R., Accardo, C.M., Rocha, H.A.O., Filgueira, L.G.A., Leite, E.L. (2013) A sulfated polysaccharide, fucans, isolated from brown algae Sargassum vulgare with anticoagulant, antithrombotic, antioxidant and anti-inflammatory effects. Carbohydr Polym 91(1): 467-475.

Duncombe, W.G. (1963) The colorimetric micro-determination of long-chain fatty acids. Biochem J 88(1): 7-10.

Duncombe, W.G. (1964) The colorimetric micro-determination of non-esterified fatty acids in plasma. Clin Chim Acta 9: 122-125.

Durand, E., Helley, D., Zen, A.A.H., Dujols, C., Bruneval, P., Colliec-Jouault, S., Fischer, A.M., Lafont, A. (2008) Effect of low molecular weight fucoidan and low molecular weight heparin in a rabbit model of arterial thrombosis. J Vasc Res 45(6): 529-537.

Durig, J., Bruhn, T., Zurborn, K.H., Gutensohn, K., Bruhn, H.D., Beress, L. (1997) Anticoagulant fucoidan fractions from Fucus vesiculosus induce platelet activation in vitro. Thromb Res 85(6): 479-491.

Ehrlich, P. (1877) Beitrage zur kenntniss der anilinfarbungen und ihrer verwendung in der mikroskopischen technik. Arch Mikrosk Anat 13: 263-277.

Elmegeed, D.F.A., Ghareeb, D.A., Elsayed, M., El-Saadani, M. (2014) Phytochemical constituents and bioscreening activities of green algae (Ulva Lactuca). IJAPR 2(11): 373-378.

Elsner, H. (1938) Über das Vorkommen von hochwirksamen, die Blutgerinnung hemmenden Stoffen in Meeresalgen. II. Hoppe-Seylers Z Physiol Chem 252(3-4): 196-200.

Elsner, H., Broser, W. Bürgel, E. (1937) Über das Vorkommen von hochwirksamen, die Blutgerinnung hemmenden Stoffen in Rotalgen. HoppeSeylers Z Physiol Chem 246(5-6): 244-247.

Faggio, C., Morabito, M., Minicante, S.A., Piano, G.L., Pagano, M., Genovese, G. (2015) Potential use of polysaccharides from the brown alga Undaria pinnatifida as anticoagulants. Braz Arch Biol Technol 58: 798-804.

Faggio, C., Pagano, M., Dottore, A., Genovese G., Morabito M. (2016) Evaluation of anticoagulant activity of two algal polysaccharides. Nat Prod Res 30: 1934-1937.

Fan, L., Jiang, L., Xu, Y., Zhou, Y., Shen, Y., Xie, W., Long, Z., Zhou, J. (2011) Synthesis and anticoagulant activity of sodium alginate sulfates. Carbohydr Polym 83(4): 1797-1803.

Farias, W.R., Nazareth, R.A., Mourao, P.A.S.(2001) Dual effects of sulfated Dgalactans from the red algae Botryocladia occidentalis preventing thrombosis and inducing platelet aggregation. Thromb Haemost 86(6): 1540-1546.

Farias, W.R., Valente, A.P., Pereira, M.S., Mourao, P.A.S. (2000) Structure and anticoagulant activity of sulfated galactans: Isolation of a unique sulfated galactan from the red algae Botryocladia occidentalis and comparison of its anticoagulant action with that of sulfated galactans from invertebrates. J Biol Chem 275(38): 29299-29307.

Fernández, P.V., Quintana, I., Cerezo, A.S., Caramelo, J.J., Pol-Fachin, L., Verli, H., Estevez, J.M., Ciancia, M. (2013) Anticoagulant activity of a unique sulfated pyranosic (1→3)-β-l-arabinan through direct interaction with thrombin. J Biol Chem 288(1): 223-233.

Fischer, A. (1931) Inhibition of blood coagulation. Biochem Z 240: 364-380.

Gollin, R.A., Michaclis, R., Waker, D., Adams, S.S. (1965) Process for the preparation of laminarin sulfates. US PATENT 3, 200, 110 A.

Güven, K.C., Aktin, E. (1962) A study on the antilipemic and anticoagulant activities of Phyllophora nervosa (D. C.) Grev. Eczacılık Bülteni 4: 199-206.

Güven, K.C., Aktin, E. (1964) Studies on antilipaemic and anticoagulant properties of the algae collected from Turkish coasts. Bot Mar 7(1-4): 1-3.

Güven, K.C., Aktin, E., Koyuncuoglu, H., Bergisadi, N. (1974a) Lipolytic and hypoglycemic compounds obtained from Cystoseira barbata. J Ag ArzneimittelForsch 24(2): 144-147.

Güven, K.C., Bora, A., Aktin, E., Öker, C., Hatemi, H., Çetin, E.T. (1972) Investigations on Phyllophora nervosa (D. C.) Grev. Bot Mar 15(1): 46-51.

Güven, K.C., Bergişadi, N., Güler, E. (1979a) A modification of Duncombe’s Method and its application to the lipolytic activity assay of heparin. Fett Wiss Technol 81(4): 152-154.

Güven, K.C., Güler, E., Aktin, E., Koyuncuoğlu, H. (1979b) Studies on Pterocladia capillacea (Gmel.) Born et Thur. Part II. In: Marine Algae in Pharmaceutical Science (eds. Hoppe, H. A., Levring, T., Tanaka, Y.) Walter de Gruyter, Berlin, New York, pp 693-710.

Güven, K.C., Güvener, B. (1985a) Metachromatic identification of (iota-,Kappa-, lambda-) carragenans. Bot Mar 28: 221-222.

Güven, K.C., Güvener, B. (1985b) A metachromatic method for identification of alginic acid, agar and carragenan. Fett Wiss Technol 87: 172-176.

Güven, K.C., Kızıl, Z. (1986) Pharmacological studies of Halopytys incurvus (Huds.) Batters (Rhodophyceae). Acta Pharm Turc 28: 47-50.

Güven, K.C., Mutluay, E., Aktin, E., Koyuncuoglu, H. (1975) Chemical and pharmacological investigations on Corallina rubens. Planta Med 27(1): 5-13.

Güven, K.C., Ozsoy, Y., Ulutin, O.N. (1991) Anticoagulant, fibrinolytic and antiaggregant activity of carregeenans and alginic acid. Bot Mar 34(5): 429-432.

Güven, K.C., Ulutin, S.B., Mutluay, E., Ulutin, O.N. (1973) Anticoagulantantithrombin and fibrinolytic actions of extract of marine alga Corallina rubens L. Pathophysiol. Haemost Thromb 2(6): 260-268.

Güven, K. C., Ulutin, S. B., Mutluay, E., Ulutin, O. N. (1974b) Anticoagulant antithrombin and fibrinolytic actions of extract of marine alga Corallina rubens L. Haemostasis 2(6): 260-268.

Haroun-Bouhedja, F., Ellouali, M., Sinquin, C., Boisson-Vidal, C. (2000) Relationship between sulfate groups and biological activities of fucans. Thromb Res 100(5): 453-459.

Hassid, W.Z. (1933) The isolation of a sodium sulfuric acid ester of galactan from Irideae Laminarioides (Rhodophyceae). J Am Chem Soc 55(10): 4163-4167.

Hawkins, W.W., Leonard, V.G. (1958) The physiological activity of laminarin sulphate. Can J Biochem Physiol 36(1): 161-170.

Hawkins, W.W., Leonard, V.G. (1962) Antipeptic and antithrombic properties of carrageenin. J Lab Clin Med 60: 641-648.

Hawkins, W.W., Leonard, V.G. (1963) The antithrombic activity of carrageenin in human blood. Can J Biochem Physiol 41: 1325-1327.

Hawkins, W.W., O’Neill, A.N. (1955) The anticoagulant action in blood of sulphated derivatives of laminarin. Can J Biochem Physiol 33(4): 545-552.

Hayakawa, Y., Hayashi, T., Lee, J.-B., Srisomporn, P., Maeda, M., Ozawa, T., Sakuragawa, N. (2000) Inhibition of thrombin by sulfated polysaccharides isolated from green algae. Biochim Biophys Acta – Prot Struct Mol Enzymol 1543(1): 86-94.

Houck, J.C., Morris, R.K., Lazaro, E.J. (1957) Anticoagulant, lipemia clearing and other effects of anionic polysaccharides extracted from seaweed. Exp Biol Med 96(2): 528-530.

Howell, W.H., Holt, L.E. (1918) Two new factors in blood coagulation-heparin and pro-antithrombin. Am J Physiol 47: 328-341.

Ibrahim, E.A., Aly, H.F., and El-Baz, F.K. (2016) Anticoagulant and antiinflammatory potentials of some Egyptian marine algae. Int J Pharma Bio Sci Blood Coagul Fibrinolysis 7(2): 89-94.

Irhimeh, M.R., Fitton, J.H., Lowenthal, R.M. (2009) Pilot clinical study to evaluate the anticoagulant activity of fucoidan. Blood Coagulation & Fibrinolysis 20(7): 607-610.

Jung, W.-K., Athukorala, Y., Lee, Y.-J., Cha, S. H., Lee, C.-H., Vasanthan, T., Choi, K.-S., Yoo, S.-H., Kim, S.-K., Jeon, Y.-J. (2007) Sulfated polysaccharide purified from Ecklonia cava accelerates antithrombin III-mediated plasma proteinase inhibition. J Appl Phycol 19(5): 425-430.

Jurd, K.M., Rogers, D.J., Blunden, G., McLellan, D.S. (1995) Anticoagulant properties of sulphated polysaccharides and a proteoglycan from Codium fragile ssp. atlanticum. J Appl Phycol 7(4): 339.

Kang, S.-R., Choi, J.-H., Kim, D.-W., Park, S.-E., Sapkota, K., Kim, S., Kim, S.-J. (2016) A bifunctional protease from green alga Ulva pertussa with anticoagulant properties: partial purification and characterization. J Appl Phycol 28(1): 599-607.

Karaki, N., Sebaaly, C., Chahine, N., Faour, T., Zinchenko, A., Rachid, S., Kanaan, H. (2013) The antioxidant and anticoagulant activities of polysaccharides isolated from the brown algae Dictyopteris polypodioides growing on the Lebanese coast. J Appl Pharm Sci 3(2): 43-51.

Kim, K.J., Lee, O.H., Lee, H.H., Lee, B.Y. (2010) A 4-week repeated oral dose toxicity study of fucoidan from the sporophyll of Undaria pinnatifida in Sprague-Dawley rats. Toxicol 267(1-3): 154-158.

Kindness, G., Long, W.F., Williamson, F.B. (1979a) Enhancement of antithrombin III activity by carrageenans. Thromb Res 15(1): 49-60.

Kindness, G., Long, W.F., Williamson, F.B., Boyd, J. (1979b) Effects of carrageenans on the aggregation of human blood platelets. Thromb Res 15(1-2): 3-15.

Kitamura, K., Matsuo, M., Yasui, T. (1991) Fucoidan from brown seaweed Laminaria angustata var. longissima. Agric Biol Chem 55(2): 615-616.

Kolender, A.A., Pujol, C.A., Damonte, E.B., Matulewicz, M.C., Cerezo, A.S. (1997) The system of sulfated alpha-(1–>3)-linked D-mannans from the red seaweed Nothogenia fastigiata: structures, antiherpetic and anticoagulant properties. Carbohydr Res 304(1): 53-60.

Kraan, S. (2012) Algal polysaccharides, novel applications and outlook. In: Carbohydrates –Comprehensive Studies on Glycobiology and Glycotechnology, (ed. Chang, C-F.), InTech, Rijeka, pp. 489-532.

Kuznetsova, T.A., Besednova, N.N., Mamaev, A.N., Momot, A.P., Shevchenko, N.M., Zvyagintseva, T.N. (2003) Anticoagulant activity of fucoidan from brown algae Fucus evanescens of the Okhotsk Sea. Bull Exp Biol Med 136(5): 471-473.

Kylin, H. (1913) Zur biochemie der meeresalgen. H-S. Z. Physiol. Chem. 83(3): 171-197.

Lee, S.-H., Athukorala, Y., Lee, J.-S., Jeon, Y.-J. (2008) Simple separation of anticoagulant sulfated galactan from marine red algae. J Appl Phycol 20(6): 1053-1059.

Li, N., Mao, W., Yan, M., Liu, X., Xia, Z., Wang, S., Xiao, B., Chen, C., Zhang, L., Cao, S. (2015) Structural characterization and anticoagulant activity of a sulfated polysaccharide from the green alga Codium divaricatum. Carbohydr Polym 121: 175-182.

Li, B., Zhao, R.-X., Wei, X.-J. (2008) Anticoagulant activity of fucoidan from Hizikia fusiforme. Agro Food Industry Hi-Tech 19(1): 22-24.

Lison, L. (1935) Etudes sur la metachromasie colorants metachromatiques et substances chromotropes. Arch Biol 46: 599-668.

Liu, J., Zhan, X., Wan, J., Wang, Y., Wang, C. (2015) Review for carrageenanbased pharmaceutical biomaterials: favourable physical features versus adverse biological effects. Carbohydr Polym 121: 27-36.

Maeda, M., Uehara, T., Harada, N., Sekiguchi, M., Hiraoka, A. (1991) Heparinoid-active sulphated polysaccharides from Monostroma nitidum and their distribution in the Chlorophyta. Phytochem 30(11): 3611-3614.

Majdoub, H., Mansour, M.B., Chaubet, F., Roudesli, M.S., Maaroufi, R.M. (2009) Anticoagulant activity of a sulfated polysaccharide from the green alga Arthrospira platensis. Biochim Biophys Acta 1790(10): 1377-1381.

Mao, W.-J., Fang, F., Li, H.-Y., Qi, X.-H., Sun, H.-H., Chen, Y., Guo, S.-D. (2008) Heparinoid-active two sulfated polysaccharides isolated from marine green algae Monostroma nitidum. Carbohydr Polym 74(4): 834-839.

Mao, W., Li, H., Li, Y., Zhang, H., Qi, X., Sun, H., Chen, Y., Guo, S. (2009) Chemical characteristic and anticoagulant activity of the sulfated polysaccharide isolated from Monostroma latissimum (Chlorophyta). Int J Biol Macromol 44(1): 70-74.

Mao, W., Zang, X., Li, Y., Zhang, H. (2006) Sulfated polysaccharides from marine green algae Ulva conglobata and their anticoagulant activity. J Appl Phycol 18(1): 9-14.

Margolis, J. (1958) The kaolin clotting time a rapid one-stage method for diagnosis of coagulation defects. J Clin Pathol 11(5): 406-409.

Matsubara, K., Matsuura, Y., Bacic, A., Liao, M., Hori, K., Miyazawa, K. (2001) Anticoagulant properties of a sulfated galactan preparation from a marine green alga, Codium cylindricum. Int J Biol Macromol 28(5): 395-399.

Matsubara, K., Matsuura, Y., Hori, K., Miyazawa, K. (2000) An anticoagulant proteoglycan from the marine green alga, Codium pugniformis. J Appl Phycol 12(1): 9.

Mauray, S., Sternberg, C., Theveniaux, J., Millet, J., Sinquin, C., TaponBretaudiere, J., Fischer, A. M. (1995) Venous antithrombotic and anticoagulant activities of a fucoidan fraction. Thromb Haemost 74(5): 1280-1285.

McLean, J. (1916) The tromboplastic action of cephalin. Am J Physiol 41: 250-257.

McMillan, R.M., MacIntyre, D.E., Gordon, J.L. (1979) Stimulation of human platelets by carrageenans. J Pharm Pharmacol 31(3): 148-152.

Melo, F.R., Pereira, M.S., Foguel, D., Mourao, P.A.S. (2004) Antithrombinmediated anticoagulant activity of sulfated polysaccharides: different mechanisms for heparin and sulfated galactans. J Biol Chem 279(20): 20824-20835.

Millet, J., Jouault, S.C., Mauray, S., Theveniaux, J., Sternberg, C., Boisson Vidal, C., Fischer, A.M. (1999) Antithrombotic and anticoagulant activities of a low molecular weight fucoidan by the subcutaneous route. Thromb Haemost 81(3): 391-395.

Molho, D., Cotte, J. (1951) Blood coagulation and anticoagulants. II. Sulfuric esters of alginates: preparation and action in vitro on the factors involved in coagulation. Bull Soc Chim Biol 33(3-4): 312-320.

Mookerjea, S., Hawkins, W.W. (1958) The antilipaemic activity of laminarin sulphate. Can J Biochem Physiol 36(3): 261-268.

Mourao, P.A. (2004) Use of sulfated fucans as anticoagulant and antithrombotic agents: future perspectives. Curr Pharm Des 10(9): 967-981.

Murata, K. (1961) Effects of carrageenin on serum lipids and atherosclerosis in rabbits. Nature 191: 189-190.

Murata, K. (1962) The effects of sulfated polysaccharides obtained from seaweeds on experimental atherosclerosis. J Gerontol 17: 30-36.

Nardella, A., Chaubet, F., Boisson-Vidal, C., Blondin, C., Durand, P., Jozefonvicz, J. (1996) Anticoagulant low molecular weight fucans produced by radical process and ion exchange chromatography of high molecular weight fucans extracted from the brown seaweed Ascophyllum nodosum. Carbohydr Res 289: 201-208.

Nishino, T., Fukuda, A., Nagumo, T., Fujihara, M., Kaji, E. (1999) Inhibition of the generation of thrombin and factor xa by a fucoidan from the brown seaweed Ecklonia kurome. Thromb Res 96(1): 37-49.

Nishino, T., Nishioka, C., Ura, H., Nagumo, T. (1994) Isolation and partial characterization of a noval amino sugar-containing fucan sulfate from commercial Fucus vesiculosus fucoidan. Carbohydr Res 255: 213-224.

Nishino, T., Yokoyama, G., Dobashi, K., Fujihara, M., Nagumo, T. (1989) Isolation, purification, and characterization of fucose-containing sulfated polysaccharides from the brown seaweed Ecklonia kurome and their bloodanticoagulant activities. Carbohydr Res 186(1): 119-129.

O’Neill, A.N. (1955) Sulphated derivatives of laminarin. Can J Chem 33(6): 1097-1101.

Pengzhan, Y., Ning, L., Xiguang, L., Gefei, Z., Quanbin, Z., Pengcheng, L. (2003) Antihyperlipidemic effects of different molecular weight sulfated polysaccharides from Ulva pertusa (Chlorophyta). Pharmacol Res 48(6): 543-549.

Percival, E., McDowell, R. (1967) Chemistry and Enzymology of Marine Algal Polysaccharides. Academic Press London, New York.

Pereira, M.G., Benevides, N.M., Melo, M.R., Valente, A.P., Melo, F.R., Mourao, P.A. (2005) Structure and anticoagulant activity of a sulfated galactan from the red alga, Gelidium crinale. Is there a specific structural requirement for the anticoagulant action? Carbohydr Res 340(12): 2015-2023.

Pereira, M.S., Mulloy, B., Mourao, P.A. (1999) Structure and anticoagulant activity of sulfated fucans. Comparison between the regular, repetitive, and linear fucans from echinoderms with the more heterogeneous and branched polymers from brown algae. J Biol Chem 274(12): 7656-7667.

Pereira, M.S., Melo, F.R., Mourão, P.A.S. (2002a) Is there a correlation between structure and anticoagulant action of sulfated galactans and sulfated fucans? Glycobiology 12(10): 573-580.

Pereira, M.S., Vilela-Silva, A.-C.E.S., Valente, A.-P., Mourão, P.A.S. (2002b) A 2-sulfated, 3-linked α-l-galactan is an anticoagulant polysaccharide. Carbohydr Res 337(21-23): 2231-2238.

Pitney, W.R., Dacie, J.V. (1953) A simple method of studying the generation of thrombin in recalcified plasma: Application in the investigation of haemophilia. J Clin Pathol 6(1): 9-14.

Pulsawat, W., Tongmalee, S. (2014) Synthesis and Anticoagulant activity of Sulfated alginate. KKU Res J 19(Suppl): 60-66.

Pushpamali, W.A., Nikapitiya, C., Zoysa, M.D., Whang, I., Kim, S. J., Lee, J. (2008) Isolation and purification of an anticoagulant from fermented red seaweed Lomentaria catenata. Carbohydr Polym 73(2): 274-279.

Qi, X., Mao, W., Chen, Y., Chen, Y., Zhao, C., Li, N., Wang, C. (2013) Chemical characteristics and anticoagulant activities of two sulfated polysaccharides from Enteromorpha linza (Chlorophyta). J Ocean Uni China 12(1): 175-182.

Qi, X., Mao, W., Gao, Y., Chen, Y., Chen, Y., Zhao, C., Li, N., Wang, C., Yan, M., Lin, C., Shan, J. (2012) Chemical characteristic of an anticoagulant-active sulfated polysaccharide from Enteromorpha clathrata. Carbohydr Polym 90(4): 1804-1810.

Quick, A.J. (1945) On the quantitative estimation of prothrombin. Am J Clin Pathol 15(12): 560-566.

Ren, D.L., Noda, H., Amano, H., Nishino, T., Nishizawa, K. (1994) Study on antihypertensive and antihyperlipidemic effects of marine-algae. Fish Sci 60(1): 83-88.

Rocha, H.A., Moraes, F.A., Trindade, E.S., Franco, C.R., Torquato, R.J., Veiga, S.S., Valente, A.P., Mourao, P.A., Leite, E.L., Nader, H.B., Dietrich, C.P. (2005) Structural and hemostatic activities of a sulfated galactofucan from the brown alga Spatoglossum schroederi. An ideal antithrombotic agent? J Biol Chem 280(50): 41278-41288.

Rodrigues, J.A.G., Vanderlei, E.D.S.O., Bessa, É.F., Magalhães, F.D.A., Paula, R.C.M.D., Lima, V., Benevides, N.M.B. (2011) Anticoagulant activity of a sulfated polysaccharide isolated from the green seaweed Caulerpa cupressoides. Braz Arch Biol Techn 54: 691-700.

Rogers, D.J., Jurd, K.M., Blunden, G., Paoletti, S., Zanetti, F. (1990) Anticoagulant activity of a proteoglycan in extracts of Codium fragile ssp. atlanticum. J Appl Phycol 2(4): 357-361.

Schimpf, K., Lenhard, J., Schaaf, G. (1969) The influence of the polysaccharide carrageenin on the clotting mechanism of the blood in the rabbit in vitro and in vivo. Thromb Diath Haemorrh 21(3): 524-33.

Schuler, W., Springer, G.F. (1957) Experimentelle antilipämiewirkung von fucoidin. Naturwissenschaften 44(8): 265-265.

Schwartz, H.J., Kellermeyer, R.W. (1969) Carrageenan and delayed hypersensitivity. II. Activation of Hageman factor by carrageenan and its possible significance. Proc Soc Exp Biol Med 132(3): 1021-1024.

Selim, S., Amin, A., Hassan, S., Hagazey, M. (2015) Antibacterial, cytotoxicity and anticoagulant activities from Hypnea esperi and Caulerpa prolifera marine algae. Pak J Pharm Sci 28(2): 525-530.

Sen, A.K., Das, A.K., Banerji, N., Siddhanta, A.K., Mody, K.H., Ramavat, B. K., Chauhan, V. D., Vedasiromoni, J. R., Ganguly, D. K. (1994) A new sulfated polysaccharide with potent blood anti-coagulant activity from the red seaweed Grateloupia indica. Int J Biol Macromol 16(5): 279-280.

Shanmugam, M., Mody, K.H., Oza, R.M., Ramavat, B.K. (2001a) Blood anticoagulant activity of a green marine alga Codium dwarkense (Codiaceae, Chlorophyta) in relation to its growth stages. Ind J Geo-Mar Sci 30(1): 49-52.

Shanmugam, M., Mody, K. H., Ramavat, B. K., Murthy, A. S. K., Siddhanta, A. K. (2002) Screening of Codiacean algae (Chlorophyta) of the Indian coasts for blood anticoagulant activity. Ind J Geo-Mar Sci 31(1): 33-38.

Shanmugam, M., Mody, K.H., Siddhanta, A.K. (2001b) Blood anticoagulant sulphated polysaccharides of the marine green algae Codium dwarkense (Boergs.) and C. tomentosum (Huds.) Stackh. Ind J Exp Biol 39: 365-370.

Shanmugam, M., Ramavat, B. K., Mody, K. H., Oza, R. M., Tewari, A. (2001c) Distribution of heparinoid-active sulphated polysaccharides in some Indian marine green algae. Ind J Geo-Mar Sci 30(4): 222-227.

Shonima, G. M., Jiji, T., Pratheesh, P. T., Kurup, G. M. (2012) Ex vivo anticoagulant activity of the polysaccharide isolated form Ulva fasciata. Int J LifeSc Bt and Pharm Res 1(2): 194-197.

Shore, B., Nichols, A.V., Freeman, N.K. (1953) Evidence for lipolytic action by human plasma obtained after intravenous administration of heparin. Proc Soc Exp Biol Med 83(2): 216-220.

Siddhanta, A.K., Shanmugam, M., Mody, K.H., Goswami, A.M., Ramavat, B.K. (1999) Sulphated polysaccharides of Codium dwarkense Boergs. from the west coast of India: chemical composition and blood anticoagulant activity. Int J Biol Macromol 26(2-3): 151-154.

Silva, T.M., Alves, L.G., de Queiroz, K.C., Santos, M.G., Marques, C.T., Chavante, S.F., Rocha, H.A., Leite, E.L. (2005) Partial characterization and anticoagulant activity of a heterofucan from the brown seaweed Padina gymnospora. Braz J Med Biol Res 38(4): 523-533.

Soeda, S., Sakaguchi, S., Shimeno, H., Nagamatsu, A. (1992) Fibrinolytic and anticoagulant activities of highly sulfated fucoidan. Biochem Pharmacol 43(8): 1853-1858.

Springer, G.F., Wurzel, H.A., McNeal, G.M., Ansell, N. J., Doughty, M.F. (1957) Isolation of anticoagulant fractions from crude fucoidin. Exp Biol Med 94(2): 404-409.

Sun, Y., Chen, X., Liu, S., Yu, H., Li, R., Wang, X., Qin, Y., Li, P. (2018) Preparation of low molecular weight Sargassum fusiforme polysaccharide and its anticoagulant activity. Chin J Oceanol Limn 36(3): 882-891.

Takemori, S. (1957a) Isolation and composition of some seaweed polysaccharide sulfates and their anticoagulant activity I. Hirasaki Igaku 8: 749-759.

Takemori, S. (1957b) Isolation and composition of some seaweed polysaccharide sulfates and their anticoagulant activity II. Hirasaki Igaku 8: 760-769.

Trento, F., Cattaneo, F., Pescador, R., Porta, R., Ferro, L. (2001) Antithrombin activity of an algal polysaccharide. Thromb Res 102(5): 457-465.

Uehara, T., Takeshita, M., Maeda, M. (1992) Studies on anticoagulant-active arabinan sulfates from the green alga, Codium latum. Carbohydr Res 235: 309-311.

Ushakova, N.A., Morozevich, G.E., Ustyuzhanina, N.E., Bilan, M.I., Usov, A.I., Nifantiev, N.E., Preobrazhenskaya, M.E. (2009) Anticoagulant activity of fucoidans from brown algae. Biochem (Moscow) 3(1): 77-83.

Ustyuzhanina, N.E., Bilan, M.I., Gerbst, A.G., Ushakova, N.A., Tsvetkova, E.A., Dmitrenok, A.S., Usov, A.I., Nifantiev, N.E. (2016) Anticoagulant and antithrombotic activities of modified xylofucan sulfate from the brown alga Punctaria plantaginea. Carbohydr Polym 136: 826-833.

Usui, T., Asari, K., Mizuno, T. (1980) Isolation of highly purified “fucoidan” from Eisenia bicyclis and its anticoagulant and antitumor activities. Agric Biol Chem 44(8): 1965-1966.

Wang, X., Zhang, Z., Yao, Z., Zhao, M., Qi, H. (2013) Sulfation, anticoagulant and antioxidant activities of polysaccharide from green algae Enteromorpha linza. Int J Biol Macromol 58: 225-230.

Wang, J., Zhang, Q., Zhang, Z., Song, H., Li, P. (2010) Potential antioxidant and anticoagulant capacity of low molecular weight fucoidan fractions extracted from Laminaria japonica. Int J Biol Macromol 46(1): 6-12.

Wijesinghe, W.A.J.P., Athukorala, Y., Jeon, Y.J. (2011) Effect of anticoagulative sulfated polysaccharide purified from enzyme-assistant extract of a brown seaweed Ecklonia cava on Wistar rats. Carbohydr Res 86(2): 917- 921.

Winter, C.A., Risley, E.A., Nuss, G.W. (1962) Carrageenin-induced edema in hind paw of the rat as an assay for antiinflammatory drugs. Exp Biol Med 111(3): 544-547.

Yoon, S. J., Pyun, Y.R., Hwang, J.K., Mourao, P.A. (2007) A sulfated fucan from the brown alga Laminaria cichorioides has mainly heparin cofactor IIdependent anticoagulant activity. Carbohydr Res 342(15): 2326-2330.

Yu, Y., Li, Y.P., Du, C.Y., Mou, H.J., Wang, P. (2017) Compositional and structural characteristics of sulfated polysaccharide from Enteromorpha prolifera. Carbohydr Polym 165: 221-228.

Yuan, Y., Xu, X., Jing, C., Zou, P., Zhang, C., Li, Y. (2018) Microwave assisted hydrothermal extraction of polysaccharides from Ulva prolifera: Functional properties and bioactivities. Carbohydr Polym 181: 902-910.

Zha, X.Q., Xiao, J.J., Zhang, H.N., Wang, J.H., Pan, L.H., Yang, X.F., Luo, J.P. (2012) Polysaccharides in Laminaria japonica (LP): Extraction, physicochemical properties and their hypolipidemic activities in diet-induced mouse model of atherosclerosis. Food Chem 134: 244-252.

Zhang, H., Mao, W., Fang, F., Li, H., Sun, H., Chen, Y., Qi, X. (2008) Chemical characteristics and anticoagulant activities of a sulfated polysaccharide and its fragments from Monostroma latissimum. Carbohydr Res 71(3): 428-434.

Zhang, Z., Till, S., Jiang, C., Knappe, S., Reutterer, S., Scheiflinger, F., Szabo, C.M., Dockal, M. (2014) Structure-activity relationship of the pro- and anticoagulant effects of Fucus vesiculosus fucoidan. Thromb Haemost 111(3): 429-437.

Zhang, Z., Zhang, Q., Wang, J., Song, H., Zhang, H., Niu, X. (2010) Regioselective syntheses of sulfated porphyrans from Porphyra haitanensis and their antioxidant and anticoagulant activities in vitro. Carbohydr Res 79(4): 1124-1129.

Zhao, T., Zhang, Q., Qi, H., Zhang, H., Niu, X., Xu, Z., Li, Z. (2006) Degradation of porphyran from Porphyra haitanensis and the antioxidant activities of the degraded porphyrans with different molecular weight. Int J Biol Macromol 38(1): 45-50.

Zúñiga, E.A., Matsuhiro, B., Mejías, E. (2006) Preparation of a low-molecular weight fraction by free radical depolymerization of the sulfated galactan from Schizymenia binderi (Gigartinales, Rhodophyta) and its anticoagulant activity. Carbohydr Polym 66(2): 208-215.

EUROPEN UNİON (EU) RİSK ASSESSMENT OF PLOTOSUS LİNEATUS (THUNBERG, 1787); A SUMMARY AND İNFORMATİON UPDATE

Europen Union (EU) Risk Assessment of Plotosus lineatus (Thunberg, 1787); a summary and information update

Marika Galanidi, Cemal Turan, Bayram Öztürk, Argyro Zenetos

Institute of Marine Sciences and Technology, Dokuz Eylül University, Izmir, TURKEY
Marine Science and Technology Faculty, Iskenderun Technical University, Iskenderun, TURKEY
Faculty of Aquatic Sciences, Istanbul University, Istanbul, TURKEY
Turkish Marine Research Foundation (TUDAV), P.O. Box: 10, Beykoz, Istanbul, TURKEY
Hellenic Centre for Marine Research, Attiki, GREECE

Abstract

Plotosus lineatus is a venomous Lessepsian fish species present in the south-eastern Mediterranean since 2002. It has been identified as one of the priority marine invasive alien species (IAS) likely to threaten native ecosystems and human well-being throughout the Mediterranean and within EU marine waters. It was thus selected as one of the species to be risk assessed and considered for management under the EU IAS Regulation. This work describes the main findings of the Risk Assessment (RA) of P. lineatus and discusses possible management measures. The species has a high likelihood to enter the RA area through natural dispersal and the possibility of “facilitated” or accidental escapes from domestic or public/private aquaria, has been established in some parts of the Mediterranean and is very likely to establish throughout the Mediterranean and possibly the Black Sea. Potential population explosions can instigate major environmental impacts on native community structure and ecosystem functions through competition, predation and habitat use; additionally, its painful and potentially dangerous sting poses a serious health risk. The risk assessment identified a moderate rate of spread due to depth limitations to dispersal, which can facilitate population control and containment efforts, should they be needed. Commercialization of the species for consumption and biomedical research can be an option for long-term management.

Keywords: Plotosus lineatus, striped eel catfish, invasive, risk assessment, management measures, EU IAS Regulation

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References

Adriaens, T., Vandegehuchte, M., Casaer, J. (2018) Guidance for Drafting Best Management Practices for Invasive Alien Species. Reports of the Research Institute for Nature and Forest 2018 (68). Research Institute for Nature and Forest, Brussels.

Ali, M., Saad, A., Soliman, A. (2015) Expansion confirmation of the IndoPacific catfish, Plotosus lineatus (Thunberg, 1787), (Siluriformes : Plotosidae) into Syrian marine waters. American Journal of Biology and Life Sciences 3: 7- 11.

Ali, M., Saad, A., Ali, A. L., Capapé, C. (2017) Additional records of striped eel catfish Plotosus lineatus (Osteichthyes: Plotosidae) from the Syrian Coast (Eastern Mediterranean). Thalassia Salentina 39: 3-8.

Andaloro, F., Castriota, L., Falautano, M., Azzurro, E., Deidun, A., FenechFarrugia, A. (2016) Public feedback on early warning initiatives undertaken for hazardous non-indigenous species: the case of Lagocephalus sceleratus from Italian and Maltese waters. Management of Biological Invasions 7(4): 313-319.

Arndt, E., Givan, O., Edelist, D., Sonin, O., Belmaker, J. (2018) Shifts in eastern Mediterranean fish communities: Abundance changes, trait overlap, and possible ompetition between native and non-native species. Fishes 19: 3-15.

Azzurro, E., Stancanelli, B., Di Martino, V., Bariche, M. (2017) Range expansion of the common lionfish Pterois miles (Bennett, 1828) in the Mediterranean Sea: an unwanted new guest for Italian waters. BioInvasions Records 6 (2): 95-98.

Bacher, S., Blackburn, T. M., Essl, F., Genovesi, P., Heikkilä, J. Jeschke, J.M., Jones, G., Keller, R., Kenis, M., Kueffer, C., Martinou, A.F., Nentwig, W., Pergl, J., Pyšek, P., Rabitsch, W., Richardson, D.M., Roy, H.E., Saul, W.C., Scalera, R., Vilà, M., Wilson, J.R.U., Kumschick, S. (2018) Socio-economic impact classification of alien taxa (SEICAT). Methods in Ecology and Evolution 9: 159-168.

Barbour, A.B., Allen, M.S., Frazer, T.K., Sherman, K.D. (2011) Evaluating the potential efficacy of invasive lionfish (Pterois volitans) removals. PLoS ONE 6(5): e19666.

Bentur, Y., Altunin, S., Levdov, I., Golani, D., Spanier, E., Edelist, D., Lurie, Y. (2018) The clinical effects of the venomous Lessepsian migrant fish Plotosus lineatus (Thunberg, 1787) in the southeastern Mediterranean Sea. Clinical Toxicology 56(5): 327-331.

Biondo, M.V. (2017) Quantifying the trade in marine ornamental fishes into Switzerland and an estimation of imports from the European Union. Global Ecology and Conservation 11: 95-105.

Bitar, G. (2013) Sur la presence des poissons exotiques nouveaux de la cote Libanaise (Mediterranee orientale). Rapport Commission Internationale Mer Méditerranée 40: 592.

Blackburn, T. M., Essl, F., Evans, T., Hulme, P. E., Jeschke, J. M. et al. (2014) A unified classification of alien species based on the magnitude of their environmental impacts. PLoS Biology 12(5): e1001850.

Booy, O., Mill, A.C., Roy, H.E., Hiley, A., Moore, N., Robertson, P., Baker, S., Brazier, M., Bue, M., Bullock, R., Campbell, S., Eyre, D., Foster, J., HattonEllis, M., Long, J., Macadam, C., Morrison-Bell,C., Mumford, J., Newman, J., Parrott, D., Payne, R., Renals, T., Rodgers, E., Spencer, M., Stebbing, P., Sutton-Croft, M., Walker, K.J., Ward, A., Whittaker, S., Wyn, G. (2017) Risk management to prioritise the eradication of new and emerging invasive nonnative species. Biological Invasions 19(8): 2401-2417.

CBD (2014) Pathways of Introduction of Invasive Species, Their Prioritization and Management. UNEP/CBD/ SBSTTA/ 18/9/Add.1. Secretariat of the Convention on Biological Diversity, Montréal.

Chan, T., Sadovy, Y. (2000) Profile of the marine aquarium fish trade in Hong Kong. Aquarium Sciences and Conservation 2: 197-213.

Clark, E., Nelson, D. R., Stoll, M. J., Kobayashi, Y., Park, C., Minato-ku, K. (2011) Swarming, diel movements, feeding and cleaning behavior of juvenile venomous eel tail catfishes, Plotosus lineatus and P. japonicus (Siluriformes: Plotosidae). Aqua, International Journal of Ichthyology 17(4): 211-239.

Cline, J. M., East, T. L., Threlkeld, S. T. (1994) Fish interactions with the sediment-water interface. Hydrobiologia 275: 301-311.

DEH-Australian Government (2005) Assessment of the Western Australian Marine Aquarium Fish Fishery.

Doğdu, S., Uyan, A., Uygur, N., Gürlek, M., Ergüden, D., Turan, C. (2016) First record of the Indo-Pacific striped eel catfish, Plotosus lineatus (Thunberg, 1787), from Turkish marine waters. Natural and Engineering Sciences 1(2): 25- 32.

EC (2011) Our Life Insurance, Our Natural Capital: an EU Biodiversity Strategy to 2020. COM/2011/244, European Commission, Brussels.

EC (2018) Study on Invasive Alien Species. Development of Risk Assessments to Tackle Priority Species and Enhance Prevention: Final Report. Publications Office of the European Union, Brussels.

Edelist, D., Golani, D., Rilov, G., Spanier, E. (2012) The invasive venomous striped eel catfish Plotosus lineatus in the Levant: Possible mechanisms facilitating its rapid invasional success. Marine Biology 159: 283-290.

EU (2014) Regulation (EU) No 1143/2014 of the European Parliament and of the Council of 22 October 2014 on the prevention and management of the introduction and spread of invasive alien species. Official Journal of the European Union 317: 35-55.

Fahim, F. A., Mady, E. A., Ahmed, S. M., Zaki, M. A. (1996) Biochemical studies on the effect of Plotosus lineatus crude venom (in vivo) and its effect on eac-cells (in vitro). In: Natural Toxins 2: Structure, Mechanism of Action, and Detection, (eds. Singh, B. R. and Tu, A. T.) Springer US, Boston,pp.343-355.

FAO (2016) The State of the Mediterranean and Black Sea Fisheries 2016. General Fisheries Commission for the Mediterranean, Rome, Italy.

Fischer, W., Sousa, I., Silva, C., de Freitas, A., Poutiers, J.M., Schneider, W., Borges, T.P., Feral, J.P., Massinga, A. (1990) Fichas FAO de identificaçao de espècies para actividades de pesca. Guia de campo das espècies comerciais marinhas e de águas salobras de Moçambique. Roma, FAO.

Froese, R., Pauly, D. (Eds). (2019) FishBase. World Wide Web electronic publication. www.fishbase.org

Galanidi, M., Zenetos, A., Bacher, S. (2018) Assessing the socio-economic impacts of priority marine invasive fishes in the Mediterranean with the newly proposed SEICAT methodology. Mediterranean Marine Science 19(1): 107-123.

GFCM-UNEP/MAP (2017) Sub-Regional Pilot Study for the Eastern Mediterranean on Non-Indigenous Species in Relation to Fisheries Background Paper. UNEP (DEPI)/MED WG.445/3.

GFCM-UNEP/MAP (2018) Report of the Joint GFCM-UN Environment/MAP Subregional Pilot Study for the Eastern Mediterranean on Non-indigenous Species in Relation to Fisheries.

Goh, N. K. C., Goh, B. P. L. (1989) A study of the hydrobiological conditions of Sungei Serangoon. In: Coastal Living Resources of Singapore: Proceedings of a Symposium on the Assessment of Living Resources in the Coastal Areas of Singapore, pp.45-51.

Golani, D. (2002) The Indo-Pacific striped eel catfish, Plotosus lineatus (Thunberg, 1787), (Osteichthyes: Siluriformes) a new record from the Mediterranean. Scientia Marina 66: 321-323.

Gweta, S., Spanier, E., Bentur, Y. (2008) Venomous fish injuries along the Israeli Mediterranean coast: Scope and characterization. Israel Medical Association Journal 10 (11): 783-788.

Haddad Jr., V. (2016) Medical Emergencies Caused by Aquatic Animals. A Zoological and Clinical Guide. Springer.

Heo, S.I., Ryu, Y.W., Rho, S., Lee, C. H., Lee, Y.D. (2007) Reproductive cycle of the striped eel catfish Plotosus lineatus (Thunberg). Journal of the Korean Fisheries Society 40: 141-146 (in Korean with English abstract).

IPCC (2013) Climate Change 2013: The Physical Science Basis. Contribution of Working Group I to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change (eds., Stocker, T.F., Qin, D. Plattner, G.-K. Tignor, M. Allen, S.K. Boschung, J. Nauels, A. Xia, Y. Bex, V. Midgley, P.M.), Cambridge University Press, Cambridge and New York.

IUCN (2017) Guidance for Interpretation of CBD Categories on Introduction Pathways. Technical note prepared by IUCN for the European Commission.

Job, S.V. (1959) The metabolism of Plotosus anguillaris (Bloch) in various concentrations of salt and oxygen in the medium. Proceedings of the Indian Academy of Sciences – Section B 50: 267.

Karachle, P.K., Corsini-Foka, M., Crocetta, F., Dulcic, J., Djhembekova, N. et al. (2017) Setting up a billboard of marine invasive species in the ESENIAS area: current situation and future expectancies. Acta Adriatica 58 (3): 429-458.

Kolbadinezhad, S., Coimbra, J., Wilson, J.M. (2018) Osmoregulation in the Plotosidae catfish: role of the salt secreting dendritic organ. Frontiers in Physiology 9: 761.

Leal, M.C., Vaz, M.C., Puga, J., Rocha, R.J., Brown, C., Rosa, R., Calado, R. (2016) Marine ornamental fish imports in the European Union: an economic perspective. Fish and Fisheries 17: 459-468.

Leis, J. M. (1991) The pelagic stage of reef fishes: the larval biology of coral reef fishes. In: The Ecology of Fishes on Coral Reefs, (ed. P. F. Sale), Academic Press, Inc., pp. 183-230.

Leis, J. M. (1993) Larval fish assemblages near Indo-Pacific coral reefs. Bulletin of Marine Science 53: 362-392.

Levin, L. A. (2006) Recent progress in understanding larval dispersal: New directions and digressions. Integrative and Comparative Biology 46 (3): 282–297.

Manikandarajan, T., Eswar, A., Anbarasu, R., Ramamoorthy, K., Sankar, G. (2014) Proximate, Amino Acid, Fatty Acid, Vitamins and Mineral analysis of Catfish, Arius maculatus and Plotosus lineatus from Parangipettai South East Coast of India. IOSR Journal of Environmental Science, Toxicology and Food Technology 8 (5): 32-40.

Moriuchi, S., Dotsu, Y. (1973) The spawning and the larva rearing of the sea catfish Plotosus anguillaris. Bulletin of the Faculty of Fisheries Nagasaki University 36: 7-12 (in Japanese with English abstract).

Murray, J.M., Watson, G.J. (2014) A critical assessment of marine aquarist biodiversity data and commercial aquaculture: Identifying gaps in culture initiatives to inform local fisheries managers. PLoS One 9(9): e105982.

OBIS (2017) Distribution records of Plotosus lineatus (Thunberg, 1787) Available: Ocean Biogeographic Information System. Intergovernmental Oceanographic Commission of UNESCO. www.iobis.org. (Accessed 15 Jun 2017)

Otero, M., Cebrian, E., Francour, P., Galil, B., Savini, D. (2013) Monitoring Marine Invasive Species in Mediterranean Marine Protected Areas (MPAs): A Strategy and Practical Guide for Managers. IUCN, Malaga, Spain.

Ounifi-Ben Amor, K., Rifi, M., Ghanem, R., Draief, I., Zaouali, J., Souissi, J. B. E. N. (2016) Update of alien fauna and new records from Tunisian marine waters. Mediterranean Marine Science 17: 124-143.

Rhyne, A. L., Tlusty, M. F., Schofield, P. J., Kaufman, L., Morris, J. A., Bruckner, A. W. (2012) Revealing the appetite of the marine aquarium fish trade: The volume and biodiversity of fish imported into the united states. PLoS One 7(5): e35808.

Roy, H.E., Rabitsch, W., Scalera, R., Stewart, A., Gallardo, B., Genovesi, P., Essl, F., Adriaens, T., Bacher, S., Booy, O., Branquart, E., Brunel, S., Copp, G.H., Dean, H., D’hondt, B., Josefsson, M., Kenis, M., Kettunen, M., Linnamagi, M., Lucy, F., Martinou, A., Moore, N., Nentwig, W., Nieto, A., Pergl, J., Peyton, J., Roques, A., Schindler, S., Schönrogge, K., Solarz, W., Stebbing, P.D., Trichkova, T., Vanderhoeven, S., Valkenburg, J.v., Zenetos, A. (2017) Developing a framework of minimum standards for the risk assessment of alien species. Journal of Applied Ecology 55: 526-538.

Roy, H.E., Adriaens, T., Aldridge, D.C., Bacher, S., Bishop, J.D.D., Blackburn, T.M., Branquart, E., Brodie, J., Carboneras, C., Cook, E.J., Copp, G.H., Dean, H., Eilenberg, J., Essl, F., Gallardo, B., Garcia, M., García-Berthou, E., Genovesi, P., Hulme, P.E., Kenis, M., Kerckhof, F., Kettunen, M., Minchin, D., Nentwig, W., Nieto, A., Pergl, J., Pescott, O., Peyton, J., Preda, C., Rabitsch, W., Roques, A., Rorke, S., Scalera, R., Schindler, S., Schönrogge, K., Solarz, W., Stewart, A., Tricarico, E., Vanderhoeven, S., Velde, G.v.d., Vilà, M., Wood, C., Zenetos, A.(2015) Invasive Alien Species – Prioritising prevention efforts through horizon scanning. ENV.B.2/ETU/2014/0016. European Commission.

Roy, H.E., Bacher, S., Essl, F., Adriaens, T., Aldridge, D.C., Bishop, J.D.D., Blackburn, T. M., Branquart, E., Brodie, J., Carboneras, C., Cottier-Cook, E.J., Copp, G.H., Dean, H., Eilenberg, J., Gallardo, B., Garcia, M., García-Berthou, E., Genovesi, P., Hulme, P.E., Kenis, M., Kerckhof, F., Kettunen, M., Minchin, D., Nentwig, W., Nieto, A., Pergl, J., Pescott, O., Peyton, J., Preda, C., Roques, A., Rorke, S.L., Scalera, R., Schindler, S., Schönrogge, K., Sewell, J., Solarz, W., Stewart, A.J.A., Tricarico, E., Vanderhoeven, S., Velde, G.v.d., Vilà, M., Wood, C.A., Zenetos, A., Rabitsch, W. (2018) Developing a list of invasive alien species likely to threaten biodiversity and ecosystems in the European Union. Global Change Biology 25: 1032-1048.

Sambrook, K., Holt, R.H.F., Sharp, R., Griffith, K., Roche, R.C., Newstead, R.G., Wyn, G., Jenkins, S.R. (2014) Capacity, capability and cross-border challenges associated with marine eradication programmes in Europe: the attempted eradication of an invasive non-native ascidian, Didemnum vexillum in Wales, United Kingdom. Marine Policy 48: 51-58.

Shiomi, K., Takamiya, M., Yamanaka, H., Kikuchi, T., Suzuki, Y. (1988) Toxins in the skin secretion of the oriental catfish (Plotosus lineatus): immunological properties and immunocytochemical identification of producing cells. Toxicon 26: 353-361.

Sin, Y. M., Wong, M. K., Chou, L. M., Alias, N. B. (1991) A study of the heavy metal concentrations of the Singapore River. Environmental Monitoring and Assessment 19: 481-494.

Temraz, T., Ben Souissi, J. (2013) First record of striped eel catfish Plotosus lineatus (Thunberg, 1787) from Egyptian waters of the Mediterranean. Rapport Commission Internationale Mer Méditerranée 40: 604.

Thresher, R. (1984) Reproduction in Reef Fishes. Neptune City: T.F.H. Publications, USA.

Turan, C., Gürlek, M., Dağhan, H., Demirhan, S.A., Karan, S. (2019) First clinical case of the venomous Lessepsian migrant fish Plotosus lineatus in Iskenderun Bay, the Northeastern Mediterranean Sea. Natural and Engineering Sciences, in progress.

UNEP/MAP (2017a) Action Plan concerning Species Introductions and Invasive Species in the Mediterranean Sea. UNEP/MAP Athens, Greece.

UNEP/MAP (2017b) 2017 Mediterranean Quality Status Report. UNEP/MAP Athens, Greece.

Vijayakumaran, K. (1997) Growth and mortality parameters and some aspects of biology of striped eel catfish Plotosus lineatus (Thunberg) from north Andhra Pradesh coast. Journal of the Marine Biological Association of India 39: 108-112.

Williams, S.L., Grosholz, E.D. (2008) The invasive species challenge in estuarine and coastal environments: Marrying management and science. Estuaries and Coasts 31: 3-20.

Yahel, R., Yahel, G., Genin, A., Steinitz, H. (2002) Daily cycles of suspended sand at coral reefs: A biological control. Limnology and Oceanography 47: 1071-1083.

STATUS OF MARINE ALIEN SPECIES ALONG THE LIBYAN COAST

Status of marine alien species along the Libyan coast

Esmail Shakman, Khaled Eteayb, Ibrhim Taboni, Abdallha Ben Abdalha

Department of Zoology, Faculty of Science, Tripoli University, LIBYA

Abstract

The number of marine alien species in Libyan waters has increased from 63 (known until the end of 2013) to 73 in the present study. This work deals with the present status, distribution and characteristics of marine alien species and their impacts along the coast of Libya, almost 2000 km long. The highest percentage was fishes (32.88%), followed by macrophytes (21.92%), molluscs (16.44%), crustaceans (13.70%), and parasites (9.59%). Some of these species have successfully adapted themselves to various topographies and habitats in the Libyan coasts, which resulted in the change in biodiversity in the area. Some fish were accompanied by parasites and others have become hosts for native parasites; seven alien parasite species (Nybelinia africana, Neoallolepidapedon hawaiins, Allolepidapedon petimba, Glyphidohaptor plectocirra, Tetrancistrum polymorphum, Apounurs sigani and Hatschekia siganicola) were recorded in three lessepsian fish species. Moreover, the toxic effect of poisonous fish (Lagocephalus sceleratus) was investigated as it caused fatalities and severe intoxication for some fishermen. Its population has dramatically increased, with high numbers of juveniles and adults reported in some bays especially in the eastern part of Libya. Alien Siganus spp. have competed with the native herbivore fish Sarpa salpa. Furthermore, some alien fishes have become commercially valuable in Libya. This paper highlights the biological invasion in the Libyan coasts in an attempt to fill the gap of knowledge on the alien species in the southeastern Mediterranean coast.

Keywords: Bioinvasion, migrant species, South Mediterranean, Libya

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References

Abdelnor, Z., Niver, L., Bauselw, W., AL-Sharief, R., Ben zegalam S., Shakman, E. (2019) Parasite fauna of the herbivorous fish Siganus luridus (Ruppell, 1829), Siganus rivulatus (Forsskal, 1775) and Sarpa salpa (Linnaeus, 1758) in the western coast of Libya. 1st Mediterranean Symposium on the NonIndigenous Species (Antalya, Turkey, 17-18 January 2019).

Al-Hassan, L., El-Silini, O. (1999) Check-list of bony fishes collected from the Mediterranean coast of Benghazi, Libya. Revista de Biologia Marina y Oceanografia 34: 291-301.

Al-Mabruk, S., Rizgalla J. (2019) First record of lionfish (Scorpaenidae: Pterois) from Libyan waters. J Black Sea/Medit Environ 25(1): 108-114.

Al-Mabruk, S., Stoilas, V., Kleitou, P., Giovos, L. (2018) The first record of Torquigener flavimaculosus (Tetraodontiformes: Tetraodontidae) from Libya. International Journal of Fisheries and Aquatic Studies 6(4): 449-450.

Al-Razagi, S. (2017) Biological Aspects of Alien Fishes Siganus luridus (Rüppell, 1829) and Siganus rivulatus (Forsskål, 1775) and Native Fish Sarpa salpa (Linnaeus, 1758) in the Western Coast of Libya. MSc. Thesis (Unpublished) Tripoli University, Libya.

Anderekis, N., Procaccini, G., Kooistra, W. (2004) Asparagopsis taxiformis and Asparagopsis armata (Bonnemaisoniales, Rhodophyta): genetic and morphological identification of Mediterranean populations. Eur J Phycol 39: 273-283.

Arndt, E., Schembri, P. (2015) Common traits associated with establishment and spread of Lessepsian fishes in the Mediterranean Sea. Mar Biol 162(10): 2141-2153.

Aydin, M. (2011) Growth, reproduction and diet of puffer fish (Lagocephalus sceleratus Gmelin, 1789) from Turkey’s Mediterranean Sea Coast. Turkish Journal of Fisheries and Aquatic Sciences 11: 589-596.

Azzurro, E., Ben Souissi, J., Boughedir, W., Cast Riota, L., Deidun, A. (2014) The Sicily Strait: A transnational observatory for monitoring the advance of non-indigenous species. Biologia Marina Mediterranea 21(1): 105-106.

Azzurro, E., Stancanelli, B., Di Martino, V., Bariche, M. (2017) Range expansion of the common lionfish Pterois miles (Bennett, 1828) in the Mediterranean Sea: an unwanted new guest for Italian waters. BioInvasions Records (6)2: 95-98.

Bazairi, H., Sghaier, Y., Benamer, I., Langarh, H., Pergent, G., Borass, E., Verlaque, M., Ben Souissi, J., Zenetos, A. (2013) Alien marine species of Libya: first inventory and new records in El-Kouf National Park (Cyrenaica) and the neighboring areas. Mediterranean Marine Science 14(2): 451-462.

Belmaker, J., Brokovich, E., China, V., Golani, D., Kiflawi, M. (2009) Estimating the rate of biological introductions: Lessepsian fishes in the Mediterranean. Ecology 90: 1134-1141.

Ben Abdallah, A., Al-Turky A., Fituri, A. (2003) Commercially exploited exotic fishes in Libya. Bulletin de l’Institut National des Sciences et Technologies de la Mer (Salammbô) n°spécial 8: 53-55.

Ben Abdallah, A., Al Turky A., Fituri, A. (2004) New records of invasive fishes in the western Libyan coast. Bulletin de l’Institut National des Sciences et Technologies de la Mer (Salammbô) n°spécial 9: 117-118.

Ben Abdalha, A., Al Turky, A., Fituri, A. (2005) Exotic fishes along the coast of Libya. Libyan Journal of Marine Science 10: 48-56. (in Arabic with English abstract)

Ben Amor K., Rifi M., Ghanem R., Draief I., Zaouali J., Ben Souissi J. (2016) Update of alien fauna and new records from Tunisian marine waters. Medit Mar Sci (17)1: 124-143.

Ben Souissi, J., Goani, D., Meiri, H., Ben Salem, M., Capape, C. (2007) First confirmed record of the Halave’s guitarfish, Rhinobatos halavi (Forsskäl, 1775) (Chondrichthyes: Rhi-nobatidae) in the Mediterranean Sea with a description of a case of albinisim in elasmobranches. Cahiers de Biologie Marine 48: 67-75.

Ben Tuvia, A. (1966) Red Sea fishes recently found in the Mediterranean. Copeia 2: 254-275.

Ben Tuvia, A. (1978) Immigration of fishes through the Suez Canal. Fishery Bulletin 76(1): 249-255.

Bernardi, G., Golani, D., Azzurro, E. (2010) The genetics of Lessepsian bioinvasions. In: Fish Invasions of the Mediterranean Sea: Change and Renewal, (eds., Golani, D., Applebaum-Golani, B.), Pensoft Publishers, SofiaMoscow, Russia, pp. 71-84.

Bilecenoglu, M., Taskavak, E. (2002) Characterization of Lessepsian migrant fish at Turkish sea. In: Workshop on Lessepsian Migration 20-21, July 2002 Gökceada, Turkey (eds., Öztürk, B., Basusta, N.), Turkish Marine Research Foundation, İstanbul, Turkey, pp. 87-91.

Blanc-Vernet, L., Clairefond, P., Orsolini, P. (1979) Les Foraminifères. Annales de l’Université de Provence 6: 171-209.

Boussellaa, W., Neifar, L., Goedknegt, A., Thieltges, D. (2018) Lessepsian migration and parasitism: richness, prevalence and intensity of parasites in the invasive fish Sphyraena chrysotaenia compared to its native congener Sphyraena sphyraena in Tunisian coastal waters. Peer J 6: e5558.

Bulleri, F., Bruno, J.F., Benedetti-Cecchi, L. (2008) Beyond competition: incorporating positive interactions between species to predict ecosystem invasibility. PLoS Biology 6 (e162). doi: 10.1371/journal. pbio.0060162.

Carlton, J. (1996) Biological invasions and cryptogenic species. Ecology 77: 1653-1655.

Colautti, R., Ricciardi, A., Grigorovitch, A. (2004) Is invasion success explained by the enemy release hypothesis? Ecol Lett 7(8): 721-733.

Corrales, X., Ofir, E,. Coll, M., Goren, M., Edelist D., Heymans J., Gal, G. (2017) Modeling the role and impact of alien species and fisheries on the Israeli marine continental shelf ecosystem. Journal of Marine Systems 170: 88-102.

Crise, A., Kaberi, H., Ruiz, J. (2015) A MSFD complementary approach for the assessment of pressures, knowledge and data gaps in Southern European Seas: The PERSEUS experience. Marine Pollution Bulletin doi: 10.1016/j.mar polbul.2015.03.024.

Crocetta, F., Agius, D., Balistreri, P., Bariche, M., Bayhan, Y., Çakir, M., Ciriaco, S., Corsini-Foka, M., Deidun, A., Zrelli, R., Ergüden, D., Evans, J., Ghelia, M., Giavasi, M., Kleitou, P., Kondylatos, G., Lipej, L., Mifsud, C., Özvarol, Y., Pagano, A., Portelli, P., Poursanidis, D., Rabaoui, L., Schembri, P., Taşkin, E., Tiralongo, F., Zenetos, A. (2015) New Mediterranean Biodiversity Records (October 2015). Mediterranean Marine Science 16: 682-702.

Davidson, A., Campbell, M., Hewitt, C., Schaffelke, B. (2014) Assessing the impacts of non-indigenous marine macroalgae: an update of current knowledge. Botanica Marina 58 (2): 55-79.

De Toni, G., Levi, D. (1888) Pugillo di alghe tripolitane. Rendiconti della Reale Accademia Nazionale dei Lincei, Roma, Serie 4, 4, 240-250.

Edelist, D., Rilov, G., Golani, D., Carlton, J. T., Spanier, E. (2013) Restructuring the sea: profound shifts in the world’s most invaded marine ecosystem. Diversity and Distributions 19(1): 69-77.

Elkrwe, H., Elhawaj, H., Galil, B., Ben Abdallah, A. (2008) The first record of Percnon gibbesi (H. Milne-Edwards, 1853) (Crustacea: Decapoda: Plagusiidae) from the southern rim of the Mediterranean. Aquatic Invasions 3: 243-245.

Fricke, R., Golani, D., Appelbaum-Golani, B. (2017) Arnoglossus nigrofilamentosus n. sp., a new species of flounder (Teleostei: Bothidae) from off the Mediterranean coast of Israel, probably a new case of Lessepsian migration. Scientia Marina 81: 1-9.

Giannuzzi-Savelli, R., Pusateri, F., Palmeri A., Ebreo, C. (1994) Atlante delle Conchiglie marine del mediterraneo (1). La Conchiglia, Roma.

Giannuzzi-Savelli, R., Pusateri, F., Palmeri A., Ebreo, C. (1997) Atlante delle Conchiglie marine del mediterraneo. (2) Caenogastropoda. La Conchiglia, Roma.

Giannuzzi-Savelli, R., Pusateri, F., Palmeri, A., Ebreo, C., Coppini, M. et al. (2001) Atlante delle conchiglie marine del Mediterraneo. Vol. 7: Bivalvia Protobranchia- Pteromorphia. Evolver, Roma.

Godeh, M., Nizamuddin, M., Elmenifi, F. (1992) Marine algae from eastern coast of Libya (Cyrenaica). Pakistan Journal of Botany 24(1): 11-21.

Golani, D. (2002) Lessepsian fish migration-characterization and impact on the Eastern Mediterranean. In: Workshop on Lessepsian Migration 20-21 July 2002 Gökceada, Turkey, (eds., Öztürk, B., Basusta, N.), Turkish Marine Research Foundation, İstanbul, Turkey, pp. 1-9.

Golani, D. (2010) Colonization of the Mediterranean by Red Sea fishes via the Suez Canal – Lessepsian migration. In: Fish Invasions of the Mediterranean Sea: Change and Reneval, (eds., Golani, D., Appelbaum-Golani, B.) Pensoft Publishers, Sofia-Moscow, Russia, pp. 145-188.

Golani, D., Ors-relini, L., Massuti, E., Quignard, P. (2002) CIESM Atlas of Exotic Species in the Mediterranean. (ed., Briand, F.), Vol 1. Fishes, CIESM, Monaco.

Halim, Y. (1990) On the potential migration of Indo-Pacific plankton through the Suez Canal. Bulletin de l’Institut Océanographique de Monaco, n° special (7): 11-27.

Halim, Y., Rizkalla, S. (2011) Aliens in Egyptian Mediterranean waters. A check-list of Erythrean fish with new records. Mediterranean Marine Science 12: 479-490.

Jackson, A., Tenggardjaja, K., Perez, G., Azzurro, E., Golani, D., Bernardi, G. (2015) Phylogeography of the bluespotted cornetfish, Fistularia commersonii: a predictor of bioinvasion success? Mar Ecol 36 (4): 887-896.

Kacem-Snoussi, A., Ben Abdallah, A., El Turky, A., Ben Moussa, N. (2009) Guide to Bony fishes in Libyan waters. Marine Research Center (in Arabic).

Katsanevakis, S., Wallentinus, I., Zenetos, A., Leppakoski, E., Çinar, E. (2014) Impacts of invasive alien marine species on ecosystem services and biodiversity: a pan-European review. Aquatic Invasions 9(4): 391-423.

Katsanevakis, S., Zenetos, A., Belchior, C., Cardoso, C. (2013) Invading European Seas: assessing pathways of introduction of marine aliens. Ocean and Coastal Management 76: 64-74.

Lacerda, C., Takemoto, R, Poulin, R., Pavanelli, G. (2013) Parasites of the fish Cichla piquiti (Cichlidae) in native and invaded Brazilian basins: release not from the enemy, but from its effects. Parasitol Res 112(1): 279-288.

Langer, R. (2008) Foraminifera from the Mediterranean and the Red Sea. Aqaba-Eilat, the improbable Gulf. In: Environment Biodiversity and Preservation, (ed., Por, F.D.), Magnes Press, Jerusalem, pp. 399-417.

Lehtiniemi, M., Ojaveer, H., David, M., Galil, B., Gollasch, S. (2015) Dose of truth monitoring marine non-indigenous species to serve legislative requirements. Marine Policy 54: 26-35.

Lockwood, L., Hoopes, F., Marchetti, P. (2007) Invasion Ecology. Blackwell Publishing Ltd., Malden, USA.

MacColl, D., Chapman, S. (2010) Parasites can cause selection against migrants following dispersal between environments. Funct Ecol 24(4): 847-856.

Mannino, A., Balistreri, P., Deidun, A. (2017) The Marine Biodiversity of the Mediterranean Sea in a Changing Climate: The Impact of Biological Invasions. Mediterranean Identities — Environment, Society, Culture, Borna Fuerst-Bjelis, IntechOpen, doi: 10.5772/intechopen.69214.

Milazzo, M., Azzurro, E., Badalamenti, F. (2012) On the occurrence of the silverstripe blaasop Lagocephalus sceleratus (Gmelin, 1789) along the Libyan coast. BioInvasions Records 1(2): 135-137.

Monterosato, A. (1917) Molluschi viventi e quaternari raccolti lungo le coste della Tripolitania dall’Ing. Camillo Crema. Bollettino Zoologico Italiano Ser. (3)4: 1-28.

Negoescu, I. (1981) Contribution à l’étude des Isopodes Anthuridés (Isopoda, Anthuridae) de la Mer Méditerranée. Rapports de la Commission Internationale pour l’Exploration Scientifique de la Mer Méditerranée 27(2): 219-220.

Nizamuddin, M. (1981) Contribution to the marine algae of Libya. Dictyotales. Bibliotheca Phycologica 54: 1-122.

Nizamuddin, M. (1988) Cladophoropsis gerloffii, a new siphonocladaceous alga from the coast of Libya. Willdenowia 17: 229-234.

Nizamuddin, M. (1991) The green marine algae of Libya. Elga Publishers, Bern.

Nizamuddin, M., West, A., Meñez, G. (1979) A list of marine algae from Libya. Botanica Marina 24: 465-476.

Norman, J. (1929) Notes on fishes of the Suez Canal. Proceedings of the Zoological Society of London (2): 615-616

Nunes, L., Katsanevakis, S., Zenetos, A., Cardoso, C. (2014) Gateways to lien invasions in the European Seas. Aquatic Invasions 9(2): 133-144.

Ojaveer, H., Galil, B., Campbell, L., Carlton, T., Canning-Clode, J. (2015) Classification of non-indigenous species based on their impacts: considerations for application in marine management. PLoS Biol 13(4): e1002130.

Ortiz, M., Petrescu, Ι. (2007) The marine Amphipoda (Crustacea: Gammaridea) of the Republic of Libya, SE Mediterranean. Travaux du Muséum National d’Histoire Naturelle “Grigore Antipa” 1: 11-23.

Petersen, H. (1918) AIgae (excl. Calcareous algae). Report 01 the Danish Oeeanographie Expedition, 1908-1910, to Medit.and adjae. Seas, JI, Biol., K3, 1-20.

Por, D. (1978) Lessepsian Migration. Ecological Studies. Springer Verlag, Berlin.

RAC/SPA. (2009) Report of the MedPosidonia Project-Libya (Project to Develop the Inventorying, Mapping and Monitoring of Posidonia Meadows in Four Mediterranean Countries: Algeria, Libya, Tunisia and Turkey). RAC/SPA edition, Tunis, pp. 29.

Ramdane, Z., Trilles, P. (2007) Parasitic Copepods (Crustacea: Copepoda) from Algerian marine fishes. Zootaxa 1574: 49-68.

Rilov, G., Galil, B. (2009) Marine Bioinvasions in the Mediterranean Sea – History, Distribution and Ecology. In: Biological Invasions in Marine Ecosystems: Ecological, Management, and Geographic Perspectives (eds., Rilov, G., Crooks, J.A.), Berlin Heidelberg: Springer. pp. 549-575.

Rizgalla, J., Fridman, S., Ben Abdallah, A., Bron, J., Shinn, A. (2018) First record of the non-native sea snail Haminoea cyanomarginata Heller and Thompson, 1983 (Gastropoda: Haminoeidae) in the Southern Mediterranean Sea. BioInvasions Records (7)4: 411-414.

Röckel, D. (1986) Sensational find in the Mediterranean. La Conchiglia 18(210-211): 12.

Sala, E., Kizilkaya, Z., Yildirim, D., Ballesteros E. (2011) Alien marine fishes deplete algal biomass in the eastern Mediterranean. PLoS ONE 6(2): e17356.

Salem, O. (2017) Parasites of Invasive Fishes and Their Impact on the Western Coast of Libya. MSc. Thesis, Tripoli University, Libya.

Sax, F., Brown, H., White, P., Gaines D. (2005) Dynamics of Species Invasions. Sinauer Associates, Sunderland, MA.

Schembri P., Bodilis P., Evans J., Francour P. (2010). Occurrence of barred knifejaw, Oplegnathus fasciatus (Actinopterygii: Perciformes: Oplegnathidae), in Malta (Central Mediterranean) with a discussion on possible modes of entry. Acta Ichthyologica et Piscatoria 40(2): 101-104.

Shakman, E. (2008) Lessepsian Migrant Fish Species of the Coastal Waters of Libya: Status, Biology, Ecology. PhD Thesis, Universitat Rostock, Rostock.

Shakman, E., Ben Abdalha, A., Talha, F., Faturi, A., Bariche, M. (2017) First records of seven marine organisms of different origins from Libya (Mediterranean Sea). BioInvasions Records 6(4): 377-382.

Shakman, E., Kinzelbach, R. (2006). Halfbeak fish Hemiramphus far (Forsskål,1775) in coastal waters of Libya. Zoology in the Middle East (Heidelberg) 39: 111-112.

Shakman, E., Kinzelbach, R. (2007a) First record of the Sweeper fish Pempheris vanicolensis Cuvier, 1821 in the eastern part of the Libyan coast. Rostocker Meereskundliche Beiträge 18: 1-3.

Shakman, E., Kinzelbach, R. (2007b) Commercial fishery and fish species composition in coastal waters of Libya. Rostocker Meeresbiologische Beiträge 18: 63-78.

Shakman, E., Kinzelbach, R. (2007c) Distribution and characterization of Lessepsian migrant fishes along the coast of Libya. Acta Ichthyologica et Piscatoria 37(1): 7-15.

Shakman, E., Kinzelbach, R., Trilles, J., Bariche, M. (2009) First occurrence of native cymothoids parasites on introduced rabbitfishes in the Mediterranean Sea. Acta Parasitologica 54(4): 380-384.

Stirn, J. (1970) Some notes on western trends of Lessepsian migration. Journées Ichthyologiques, Rome, CIESM, Monaco, pp. 187-190.

Streftaris, N., Zenetos, A. (2006) Alien marine species in the Mediterranean – the 100 ‘worst invasives’ and their impact. Mediterranean Marine Science 7(1): 87-118.

Tsiamis, K., Zenetos, A., Deriu, I., Gervasini, E., Cardoso, A. (2018) The native distribution range of the European marine non-indigenous species. Aquatic Invasions 13: 187-198.

Verlaque, M., Langar, H., Hmida, A., Pergent, C., Pergent, G. (2017) Introduction of a New Potential Invader into the Mediterranean Sea: The IndoPacific Avrainvillea amadelpha (Montagne) A. Gepp & ES Gepp (Dichotomosiphonaceae, Ulvophyceae). Cryptogamie Algol 38(3): 267-281.

Verlaque, M., Ruitton, S., Mineur, F., Boudouresque, C. (2015) CIESM Atlas of Exotic Species in the Mediterranean, Vol. 4. Macrophytes. CIESM, Monaco.

Whitehead, P., Bauchot, M., Hureau, J., Nielson, J., Tortonese, E. (eds.) (1984-1986) Fishes of the north-eastern Atlantic and the Mediterranean. Vols. I, II, III, UNESCO, Paris.

WoRMS Editorial Board (2019) World Register of Marine Species. http://www.marinespecies.org (Accessed March 2019).

Zaouali, J., Ben Souissi, J., Galil, B., D’Udekem D’Acoz, C., Ben Abdellah, A. (2007a) Grapsoid crabs (Crustacea: Decapoda: Brachyura) new to the Sirte Basin, southern Mediterranean Sea – the roles of vessel traffic and climate change. JMBA2 Biodiversity Records 5770.

Zaouali, J., Ben Souissi, J., Galil, B., D’Udekem D’Acoz, C., Ben Abdellah, A. (2007b) Contribution à l’étude des peuplements actuels des substrats solides de l’étage médiolittoral de la Méditerranée méridionale. Rapports de la Commission Internationale pour l’Exploration Scientifique de la Mer Méditerranée 38: 639.

Zenetos, A. (2019) Mediterranean Sea: 30 years of biological invasions (1988 –2017). 1st Mediterranean Symposium on the Non-Indigenous Species, (17-18 January 2019 Antalya, Turkey).

Zenetos, A., Çinar, M., Crocetta, F., Golani, D., Rosso, A., Servello, G., Shenkar, N., Turon, X., Verlaque, M. (2017) Uncertainties and validation of alien species catalogues: The Mediterranean as an example. Estuar Coast Shelf Sci 191: 171-187.

Zenetos, A., Gofas, S., Morri, C., Rosso, A., Violanti, D., Garcia, Raso, J. E., Çinar, M. E., Almogi, Labin, A., Ates, A. S., Azzuro, E., Ballestros, E., Bianchi, C. N., Bilecenoglu, M., Gambi, M. C., Giangrande, A., Gravili, C., Hyamskaphzan, O., Karachle, V., Katsanevakis, S., Lipei, L., Mastrototaro, F., Mineur, F., Pancucci-Papadopoulou, M. A., Ramos, Espla, A., Salas, C., San Martin, G., Sfriso, A., Streftanris, N., Verlaque, M. (2012) Alien species in the Mediterranean Sea by 2012. A contribution to the application of European Union’s Marine trategy Framework Directive (MSFD). Part 2. Introduction trends and pathways. Mediterranean Marine Science 13(2): 328-352.

Zenetos, A., Gofas, S., Verlaque, M., Çinar, M.E., Garcia Raso, J.E., Bianchi, C. N., Morri, C., Azzuro, E., Bilecenoglu, M., Froglia, C., Siokou, I., Violanti, D., Sfriso, A., San Martin, G., Giangrande, A., Katağan, T., Ballestros, E., Ramos-Espla, A., Mastrototaro, F., Ocana, O., Zingone, A., Gambi, M.C., Streftaris, N., (2010) Alien species in the Mediterranean Sea by 2010. A contribution to the application of European Union’s Marine Strategy Framework Directive (MSFD). Part I. Spatial distribution. Mediterranean Marine Science 11(2): 381-493.

Zgozi, S., Haddoud, D., Rough, A. (2002) Influence of environmental factors on distribution and abundance of macrobenthic organisms at Al Gazala lagoon (Libya) (in Arabic) Technical Report of Marine Research Center of Tajura 23-27.

Zupanovic, S., EL-Buni, A. (1982) A contribution to demersal fish studies off the Libyan coast. Bulletin of Marine Research Centre (Tripoli-Libya) 3: 77-122.

FİRST RECORD OF AETOMYLAEUS BOVİNUS (GEOFFROY ST. HİLAİRE, 1817) (ELASMOBRANCHİİ: MYLİOBATİDAE), FROM THE SEA OF MARMARA

First record of Aetomylaeus bovinus (Geoffroy St. Hilaire, 1817) (Elasmobranchii: Myliobatidae), from the Sea of Marmara

Murat Bilecenoğlu

Department of Biology, Faculty of Arts & Sciences, Aydın Adnan Menderes University, 09010 Aydın, TURKEY

Abstract

A single female individual of Aetomylaeus bovinus (Geoffroy St. Hilaire, 1817) was observed and photographed off Soğanlıdere (Çanakkale Strait) on 15 May 2019, which represents a first record for the Sea of Marmara ichthyofauna.

Keywords: Aetomylaeus bovinus, Myliobatidae, Sea of Marmara

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References

Abdul Malak, D., Livingstone, S.R., Pollard, D., Polidoro, B.A., Cuttelod, A., Bariche, M., Bilecenoglu, M., Carpenter, K.E., Collette, B.B., Francour, P., Goren, M., Kara, M.H., Massutí, E., Papaconstantinou, C., Leonardo Tunesi, L. (2011) Overview of the Conservation Status of the Marine Fishes of the Mediterranean Sea. Gland, Switzerland and Malaga, Spain, IUCN.

Akyol, O., Aydın, İ., El Kamel, M.O., Capapé, C. (2017) Bull ray, Aetomylaeus bovinus (Geoffroy Saint‐Hilaire, 1817) (Myliobatidae) in the Mediterranean Sea and captures of juveniles from Izmir Bay (Aegean Sea, Turkey). Journal of Applied Ichthyology 33: 1200-1203.

Başusta, N., Aslan, E. (2018) Age and growth of bull ray Aetomylaeus bovinus (Chondrichthyes: Myliobatidae) from the northeastern Mediterranean coast of Turkey. Cahiers de Biologie Marine 59(1): 107-114.

Bradai, M.N., Saidi, B., Enajjar, S. (2012) Elasmobranchs off the Mediterranean and Black Sea: Status, Ecology and Biology. Bibliographic analysis. Studies and Reviews. General Fisheries Commission for the Mediterranean. No. 91. Rome, FAO.

Capapé, C. (1977) Etude du régime alimentaire de la Mourine vachette, Pteromylaeus bovinus (Geoffroy Saint-Hilaire, 1817), (Pisces, Myliobatidae) des côtes tunisiennes. Journal du Conseil Permanent international pour l’Exploration de la Mer 37(3): 214-220.

Cengiz, Ö., İşmen, A., Özekinci, U., Öztekin, A. (2011) An investigation on fish fauna of Saros Bay (Northern Aegean Sea). Afyon Kocatepe Journal of Sciences 11: 31-37 (in Turkish).

Dulčić, J., Lipej, L., Bonaca, M.O., Jenko, R., Grbec, B., Guélorget, O., Capapé, C. (2008) The bull ray, Pteromylaeus bovinus (Myliobatidae), in the northern Adriatic Sea. Cybium 32: 119-123.

Fischer, W., Bauchot, M.-L., Schneider, M. (1987) Fiches FAO d’identification des espèces pour les besoins de la pêche. (Révision 1). Méditerranée et mer Noire. Zone de pêche 37. Volume II, Vertébrés, FAO, Rome, pp. 862-864.

Froese, R., Pauly, D. (2019) Aetomylaeus bovinus (Geoffroy, 1817). Available at https://www.fishbase.org/summary/ 5011 (Accessed on 23 June 2019)

Lipej, L., Mavrič, B., Dulčić, J. (2009) Size of the bull ray, Pteromylaeus bovinus (Geoffroy Saint‐Hilaire, 1817), from the northern Adriatic. Journal of Applied Ichthyology 25(suppl.1): 103-105.

McEachran, J.D., Capapé, C. (1984) Myliobatidae. In: Fishes of the Northeastern Atlantic and the Mediterranean, (eds. Whitehead, P.J.P., Bauchot, M.-L., Hureau, J.-C., Nielsen, J., Tortonese, E.), Vol.I, UNESCO, Paris, pp. 205-207.

Mejri, H., Ben Souissi, J., Zaouali, J., El Abed, A., Guilorget, O., Capapé, C., (2004) On the recent occurrence of elasmobranch species in a perimediterranean lagoon: the Tunis Southern Lagoon (Northern Tunisia). Annales, Series Historia Naturalis 14(2): 143-158.

Walls, R.H.L., Buscher, E. (2016) Aetomylaeus bovinus. The IUCN Red List of Threatened Species 2016: e.T60127A81163810, https://www.iucnredlist.org/species/60127/81163810 (Accessed on 23 June 2019)

Weigmann, S. (2016) Annotated checklist of the living sharks, batoids and chimaeras (Chondrichthyes) of the world, with a focus on biogeographical diversity. Journal of Fish Biology 88: 837-1037.

Zogaris, S., Dussling, U. (2010) On the occurrence of the bull ray Pteromylaeus bovinus (Chondrichthyes: Myliobatidae) in the Amvrakikos Gulf, Greece. Mediterranean Marine Science 11(1): 177-184.

FİRST RECORD OF HETEROPRİACANTHUS CRUENTATUS (LACEPÈDE, 1801) (CHORDATA: PRİACANTHİDAE) İN THE MEDİTERRANEAN SEA FROM THE LEBANESE WATERS

First record of Heteropriacanthus cruentatus (Lacepède, 1801) (Chordata: Priacanthidae) in the Mediterranean Sea from the Lebanese waters

Ali Badreddine, Ghazi Bitar

Department of Marine Biology, Faculty of Sciences, Lebanese University, Hadath, Beirut, LEBANON

Abstract

Heteropriacanthus cruentatus (Lacepède, 1801) was reported for the first time in the Mediterranean Sea from the Lebanese deep sea. A photograph of the glasseye fish was posted on the social media network FacebookTM. The specimen was caught from the deep sea of Lebanon on 29 April 2019 by a recreational longline fishermen.

Keywords: Heteropriacanthus cruentatus, glasseye fish, Lebanese deep sea

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References

Al Mabruk, S.A.A., Rizgalla, J. (2019) First record of lionfish (Scorpaenidae: Pterois) from Libyan waters. J Black Sea/Medit Environ 25(1): 108-114.

Azzurro, E., Broglio, E., Maynou, F., Bariche, M. (2013) Citizen science detects the undetected: the case of Abudefduf saxatilis from the Mediterranean Sea. Management of Biological Invasions 4(2): 167-170.

Calado, R. (2006) Marine ornamental species from European waters: a valuable overlooked resource or a future threat for the conservation of marine ecosystems? Scientia Marina 70(3): 389-398.

Dooley, J., Collette, B., Aiken, K.A., Marechal, J., Pina Amargos, F., SinghRenton, S. (2015) Heteropriacanthus cruentatus (errata version published in 2017). The IUCN Red List of Threatened Species 2015: e.T16749737A115363 551.

Fernandez-Silva, I., Ho, H. C. (2017) Revision of the circumtropical glasseye fish Heteropriacanthus cruentatus (Perciformes: Priacanthidae), with resurrection of two species. Zootaxa 4273(3): 341-361.

Froese, R., Pauly D. (2019) Fish Base World Wide Web electronic publication. www.fishbase.org. (Accessed 02/2019)

Gaither, M.R., Bernal, M.A., Fernandez-Silva, I., Mwale, M., Jones, S.A., Rocha, C., Rocha, L.A. (2015) Two deep evolutionary lineages in the circumtropical glasseye Heteropriacanthus cruentatus (Teleostei, Priacanthidae) with admixture in the south-western Indian Ocean. Journal of Fish Biology 87: 715-727.

Zenetos, A., Apostolopoulos, G., Crocetta, F. (2016) Aquaria kept marine fish species possibly released in the Mediterranean Sea: first confirmation of intentional release in the wild. Acta Ichthyologica & Piscatoria 46(3): 255-262.

FİRST RECORD OF MARİVAGİA STELLATA GALİL AND GERSHWİN, 2010 (SCYPHOZOA: RHİZOSTOMEAE: CEPHEİDAE) FROM THE LEBANESE WATERS İN THE EASTERN MEDİTERRANEAN SEA

First record of Marivagia stellata Galil and Gershwin, 2010 (Scyphozoa: Rhizostomeae: Cepheidae) from the Lebanese waters in the eastern Mediterranean Sea

Ghazi Bitar, Ali Badreddine

Department of Marine Biology, Faculty of Sciences, Lebanese University, Hadath, Beirut, LEBANON

Abstract

Marivagia stellata Galil and Gershwin, 2010 was reported for the first time from the Lebanese waters in the eastern Mediterranean Sea. This Indo-Pacific jellyfish was observed in 2015 during a field work. The present note reports its details in the Lebanese waters.

Keywords: Indo-Pacific jellyfish, Marivagia stellata, Lebanese waters

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References

Abboud-Abi Saab, M., Fakhri, M., Hassoun, A. (2013) Inter-annual Variations of Water and Air Temperatures in Lebanese Coastal Waters (2000-2012). Oceanography & Sustainable Marine Production: A Challenge of Managing Marine Resources in a Changing Climate, ICOSMaP.

Abboud-Abi Saab, M., Fakhri, M., Kassab, M.-T., Mattar, N. (2005) Les sels nutritifs et le phytoplankton sur la côte sud du Liban: évaluation d’indices écologiques. Leb Sci J 6 (2): 27-43.

Abboud-Abi Saab, M., Fakhri, M., Sadek, E., Matar, N. (2008) An estimate of the environmental status of Lebanese littoral waters using nutrients and chlorophyll-a as indicators. Leb Sci J 9: 43.

Bitar, G., Ramos-Espla, A., Ocana, O., Sghaier, Y., Forcada, A., Valle, C., El Shaer, H., Verlaque, M. (2017) Introduced marine macroflora of Lebanon and its distribution on the Levantine coast. Med Mar Sci 18: 138-155.

Boero, F. (2013) Review of Jellyfish Blooms in the Mediterranean and Black Sea. Studies and Reviews No.92. FAO/GFCM, Rome.

Boero, F. (2014) Review of jellyfish blooms in the Mediterranean and Black Sea. Marine Biology Research 10(10): 1038-1039.

Brotz, L., Pauly, D. (2012) Jellyfish populations in the Mediterranean Sea. Acta Adriat 53(2): 213-232.

Galil, B.S., Gershwin, L.A., Douek, J., Rinkevich, B. (2010) Marivagia stellata gen. et sp. nov. (Scyphozoa: Rhizostomeae:  Cepheidae), another alien jellyfish from the Mediterranean coast of Israel. Aquatic Invasions 5: 331-340.

Galil, B.S., Kumar, B.A., Tiyas, A.J. (2013) Marivagia stellata Galil and Gershwin, 2010 (Scyphozoa: Rhizostomeae: Cepheidae), found off the coast of Kerala, India. BioInvasions Records 2(4): 317-318.

Gul, S., Moazzam, M., Galil, B.S. (2014) Occurrence of Marivagia stellata (Scyphozoa: Rhizostomeae: Cepheidae) along the coast of Pakistan, northern Arabian Sea. Marine Biodiversity Records 7(e112): 1-2.

Harmelin, J.G., Bitar, G., Zibrowius, H. (2016) High xenodiversity versus low native diversity in the south-eastern Mediterranean: bryozoans from the coastal zone of Lebanon. Medit Mar Sci 17: 417-439.

Lakkis, S. (2013) Le zooplancton marin du Liban (Méditerranée orientale). Biologie, Biodiversité, Biogéographie. Roma (Aracne).

Lteif, M. (2015) Biology, Distribution and Diversity of Cartilaginous Fish Species along the Lebanese Coast, Eastern Mediterranean. PhD Thesis. University of Perpignan.

Mamish, S., Durgham, H., Al-Masri, M. S. (2016) First record of the new alien sea jelly species Marivagia stellata Galil and Gershwin, 2010 off the Syrian coast. Marine Biodiversity Records 9: 23.

Mamish, S., Durgham, H., Ikhtiyar, S. (2019) First record of Porpita porpita Linnaeus, 1758 (Cnidaria, Hydrozoa) on the Syrian coast of the eastern Mediterranean Sea. SSRG International Journal of Agriculture & Environmental Science (SSRG – IJAES) 6(2).

Mariottini, G.L., Giacco, E., Pane, L. (2008) The Mauve Stinger Pelagia noctiluca (Forsskål, 1775). Distribution, ecology, toxicity and epidemiology of stings. A review. Mar Drugs 6: 496-513.

Mariottini, G.L., Pane, L., (2010) Mediterranean jellyfish venoms: a review on Scyphomedusae. Mar Drugs 8: 1122-1152.

Mizrahi, G.A., Shemesh, E., Ofwegen, L., Tchernov, D. (2015) First record of Aequorea macrodactyla (Cnidaria, Hydrozoa) from the Israeli coast of the eastern Mediterranean Sea, an alien species indicating invasive pathways. NeoBiota 26: 55-70.

MOE/UNDP/ECODIT (2011) State and Trends of the Lebanese Environment. (Ministry of the Environment; United Nations Development Program; ECODIT: Beirut).

Öztürk, B., Topaloglu, B., Sümen, S.G., Turan, C., Isinibilir, M., Aktas, S., Ozen, S. (2018) Jellyfish of the Black Sea and Eastern Mediterranean Waters. Turkish Marine Research Foundation (TUDAV), Istanbul, Turkey.

Zaatari M. (2010) Odd marine changes strike coast of Sidon. The Daily Star Lebanon. Retrieved October 17, 2010. http://www1.dailystar.com.lb/News/Lebanon-News/2010/Oct-07/59848-odd-marine-changes-strike-Coast-of sidon.ashx. (Accessed 17 Oct 2010).

Zenetos, A., Gofas, S., Morri, C., Rosso, A., Violanti, D. (2012) Alien species in the Mediterranean Sea by 2012. A contribution to the application of European Union’s Marine Strategy Framework Directive (MSFD). Part 2. Introduction trends and pathways. Medit Mar Sci 13: 328-352.

Zenetos, A., Gofas, S., Verlaque, M., Çinar, M.E., Garcia Raso, J.E. (2010) Alien species in the Mediterranean Sea by 2010. A contribution to the application of European Union’s Marine Strategy Framework Directive (MSFD). Part I. Spatial distribution. Medit Mar Sci 11(2): 318-493.

NOTES ON THE OCCURRENCE OF SMALLTOOTH SANDTİGER SHARK, ODONTASPİS FEROX (LAMNİFORMES: ODONTASPİDİDAE) FROM ANTALYA BAY, EASTERN MEDİTERRANEAN, TURKEY

Notes on the occurrence of smalltooth sandtiger shark, Odontaspis ferox (Lamniformes: Odontaspididae) from Antalya Bay, eastern Mediterranean, Turkey

Hakan Kabasakal, Erdi Bayrı

Ichthyological Research Society, Tantavi mah., Menteşoğlu cad., İdil apt., No: 30, D: 4, 34764 Ümraniye, İstanbul, TURKEY

Abstract

On 11 March 2019, a female specimen of Odontaspis ferox, was incidentally caught by a commercial bottom trawler, towed at the depths between 100 to 120 m, in Antalya Bay. Total length of the specimen was 400 cm. Based on the recent Red List assessment of Mediterranean elasmobranchs, O. ferox is a rare and endangered shark species. Capture of the mature females creates a significant threat to the survival of the species. Therefore, promoting fishermen to release live specimens, appears to be an urgent, feasible first step in the protection of this rare shark in Turkish waters.

Keywords: Smalltooth sandtiger shark, endangered, incidental catch, Levantine Basin

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References

Bilecenoğlu, M., Kaya, M., Cihangir, B., Çiçek, E. (2014) An updated checklist of the marine fishes of Turkey. Turkish Journal of Zoology 38: 901-929.

Cavanagh, R. D., Gibson, C. (2007) Overview of the Conservation Status of Cartilaginous Fishes (Chondrichthyans) in the Mediterranean Sea. IUCN, Gland, Switzerland and Malaga, Spain.

Compagno, L.J.V. (2001) Sharks of the World. An Annotated and Illustrated Catalogue of Shark Species Known to Date. Volume 2. Bullhead, mackerel and carpet sharks (Heterodontiformes, Lamniformes and Orectolobiformes). FAO Species Catalogue for Fishery Purposes. No. 1, Vol. 2. Rome, FAO.

Corsini-Foka, M. (2009) Uncommon fishes from Rhodes and nearby marine region (SE Aegean Sea, Greece). Journal of Biological Research-Thessaloniki 12: 125-133.

Damalas, D., Megalofonou, P. (2012) Occurrences of large sharks in the open waters of the southeastern Mediterranean Sea. Journal of Natural History 46: 2701-2723.

Fergusson, I.K., Graham, K.J., Compagno, L.J.V. (2008) Distribution, abundance and biology of the smalltooth sandtiger shark Odontaspis ferox (Risso, 1810) (Lamniformes: Odontaspididae). Environmental Biology of Fishes 81: 207-228.

Golani, D., Öztürk, B., Başusta, N. (2006) The Fishes of the Eastern Mediterranean. Turkish Marine Research Foundation, Istanbul, Turkey.

Graham, K.J., Pollard, D.A., Gordon, I., Williams, S., Flaherty, A.A., Fergusson, I., Dicken, M. (2016) Odontaspis ferox (errata version published in 2016). The IUCN Red List of Threatened Species: e.T41876A103433002. Available at: http://dx.doi.org/10.2305/IUCN.UK.2016-1.RLTS.T41876A2957320.en

Kabasakal, H. (2002) Elasmobranch species of the seas of Turkey. Annales Series Historia Naturalis 12: 15-22.

Lipej, L., De Maddalena, A., Soldo, A. (2004) Sharks of the Adriatic Sea. Knjižnica Annales Majora, Koper, Slovenia.

Serena, F. (2005) Field Identification Guide to the Sharks and Rays of the Mediterranean and Black Sea. FAO Species Identification Guide for Fishery Purposes, FAO, Rome.

Sperone, E., Parise, G., Leone, A., Milazzo, C., Circosta, V., Santoro, G., Paolillo, G., Micarelli, P., Tripepi, S. (2012) Spatiotemporal patterns of distribution of large predatory sharks in Calabria (central Mediterranean, southern Italy). Acta Adriatica 53: 13-24.

Storai, T., Cristo, B., Zuffa, M., Zinzula, L., Floris A., Campanile, A.T. (2006) The Sardinian large elasmobranch database. Cybium 30: 141-144.

FIRST RECORD OF PHYSOPHORA HYDROSTATICA FORSKÅL, 1775 (CNIDARIA, HYDROZOA) FOR THE TURKISH SEAS

First record of Physophora hydrostatica Forskål, 1775 (Cnidaria, Hydrozoa) for the Turkish seas

Melek İşinibilir, Kamuran Ulucam, Esin Yüksel

Department of Marine Biology, Faculty of Aquatic Sciences, Istanbul University, Istanbul, TURKEY
Cengiz Topel Cad., Serender Evleri, 103/12, Istanbul, TURKEY
Institute of Graduate Studies in Sciences, Istanbul University, Istanbul, TURKEY

Abstract

A siphonophore species Physophora hydrostatica Forskål, 1775 was observed in July 2006 in Saros Bay, the North-eastern Aegean Sea coast of Turkey. Although this species is found in the Mediterranean, it is the first record from the Turkish coastal areas.

Keywords: Physophora hydrostatica, Siphonophora, jellyfish, Aegean Sea

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References

Bouillon, J., Medel, M.D., Pagès, F., Gili, J.M., Boero, F., Gravili, C. (2004) Fauna of the Mediterranean Hydrozoa. Scientia Marina 68: 5-438.

Clark, M., A., Douglas, M., Choi, J. (2018) Biology 2e. OpenStax, Rice University, Teksas, USA.

Çınar, M.E., Yokeş, M.B., Açık, Ş., Bakır, A.K. (2014) Check-list of Cnidaria and Ctenophora from the coasts of Turkey. Turkish Journal of Zoology 38: 677-697.

Çoker, T., Akyol, O. (2018) An evaluation on the fish diversity of Saroz Bay and Gökçeada Island (Northern Aegean Sea). Turkish Journal of Maritime and Marine Sciences 4(1): 81-92.

Deidun, A., Sciberras, A. (2017) Unearthing marine biodiversity through citizen science-the spot the jellyfish and the spot the alien fish campaign case studies from the Maltese Islands (Central Mediterranean). Bulletin of the Entomological Society of Malta 9: 87.

Dunn, C.W., Wagner, G.P. (2006) The evolution of colony-level development in the Siphonophora (Cnidaria: Hydrozoa). Development Genes and Evolution 216: 743-754.

Güçlüsoy, H. (2015) Marine and coastal protected areas of Turkish Aegean Coasts. In: The Aegean Sea Marine Biodiversity, Fisheries, Conservation and Governance (eds., Katağan, T., Tokaç, A., Beşiktepe, Ş., Öztürk, B.) Turkish Marine Research Foundation (TUDAV), Istanbul, Turkey, pp. 669-684.

Haddock, S. H. D., Dunn, C. W. (2005) The complex world of siphonophores. JMBA Global Marine Environment 2: 24-25.

iNaturalist (2013) Image of hula skirt siphonophore Physophora hydrostatica https://www.inaturalist.org /observations /307989 (Accessed 13 Jun 2019).

Isinibilir, M., Yılmaz, İ.N. (2017) Jellyfish dynamics and their socioeconomic and ecological consequences in Turkish Seas. In: Jellyfish: Ecology, Distribution Patterns and Human Interactions (ed. G.L. Mariottini), Nova Publishers, New York, pp. 51-70.

Jeal, F., West, A. (1970) A check list of siphonophora from Irish waters, with a record of Physophora hydrostatica (Forskal) from the Irish coast. The Irish Naturalists’ Journal 16(11): 338-342.

Pagès, F., González, H. E., Ramón, M., Sobarzo, M., Gili, J. M. (2001) Gelatinous zooplankton assemblages associated with water masses in the Humboldt Current System, and potential predatory impact by Bassia bassensis (Siphonophora: Calycophorae). Marine Ecology Progress Series 210: 13-24.

Pugh, P.R. (1984) The diel migrations and distributions within a mesopelagic community in the north east Atlantic. 7. Siphonophores. Progress in Oceanography 13: 461-489.

Purcell, J. E. (1981) Dietary composition and diel feeding patterns of epipelagic siphonophores. Marine Biology 65(1): 83-90.

Purcell, J.E., Arai, M. N. (2001) Interactions of pelagic cnidarians and ctenophores with fish: a review. Hydrobiologia 451(1-3): 27-44.

Robison, B.H. (1995) Light in the ocean’s midwaters. Scientific American 273: 60-64.

Sari, E., Çagatay, M.N. (2001) Distribution of heavy metals in the surface sediments of the Gulf of Saros, NE Aegean Sea. Environ International 26: 169-173.

The Marine Flora & Fauna of Norway (2019) Siphonophore – Physophora hydrostatica. Available at http://www.sea water.no/fauna/cnidaria/hydrostatica.html (Accessed 11 Jun 2019).

Topçu, E.N., Martell, L., Isinibilir, M. (2017) A multispecific accumulation of gelatinous organisms in the central Aegean Sea as a case of biological evidence for unnoticed offshore events. Cahiers De Biologie Marine 58: 269-277.

Yılmaz, İ.N., Isinibilir, M., Vardar, D., Dursun, F. (2017) First record of Aequorea vitrina Gosse, 1853 (Hydrozoa) from the Sea of Marmara: a potential invader for the Mediterranean Sea. Zoology in the Middle East 63: 178-180.

OCCURRENCE OF THE SQUAT LOBSTER MUNİDA CURVİMANA A. MİLNE EDWARDS & BOUVİER, 1894 AND COLOMBUS CRAB PLANES MİNUTUS (LİNNAEUS, 1758) İN TURKEY

Occurrence of the squat lobster Munida curvimana A. Milne Edwards & Bouvier, 1894 and Colombus crab Planes minutus (Linnaeus, 1758) in Turkey

Erhan Irmak, Fikret Öndes

Faculty of Fisheries, Izmir Katip Çelebi University, Izmir, Çiğli, 35620, TURKEY

Abstract

The present study reports the first record of Munida curvimana and second record of Planes minutus in Turkish waters. A male specimen of M. curvimana was collected by a commercial set net in Antalya Bay, Turkey in 2007. A male specimen of P. minutus was found on the loggerhead sea turtle that was captured by driftnet as a bycatch in Fethiye Bay in 2005. The morphometric characteristics and the updated distribution of squat lobster and Columbus crab in the Mediterranean Sea are presented.

Keywords: Decapoda, Munida curvimana, Planes minutus, Caretta caretta, symbiosis, Eastern Mediterranean

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References

Araújo, R., Calado R. (2003) Crustáceos decápodes do Arquipélago da Madeira. Funchal (Direcção Regional do Ambiente).

Bakır, A.K., Katağan, T., Aker, H.V., Özcan, T., Sezgin, M., Ateş, A.S., Kırkım, F. (2014) The marine arthropods of Turkey. Turkish Journal of Zoology 38: 765-831.

Boudreau, S.A., Worm, B. (2012) Ecological role of large benthic decapods in marine ecosystems: a review. Marine Ecology Progress Series 469: 195-213.

Chace, F.A. (1951) The oceanic crabs of the genera Planes and Pachygrapsus. Proc US Natl Mus 101: 65-103.

Chartosia, N., Anastasiadis, D., Bazairi, H., Crocetta, F., Deidun, A., Despalatović, M., Di Martino, V., Dimitriou, N., Dragičević, B., Dulčić, J., Durucan, F., Hasbek, D., Ketsilis-Rinis, V., Kleitou, P., Lipej, L., Macali, A., Marchini, A., Ousselam, M., Piraino, S., Stancanelli, B., Theodosiou, M., Tiralongo, F., Todorova, V., Trkov, D., Yapici, S. (2018) New Mediterranean biodiversity records (July 2018). Mediterranean Marine Science 19: 398-415.

Corsini-Foka, M., Pancucci-Papadopoulou, M.A. (2012) Inventory of Crustacea Decapoda and Stomatopoda from Rhodes Island (Eastern Mediterranean Sea), with emphasis on rare and newly recorded species. Journal of Biological Research Thessaloniki 19: 359-371.

Davenport, J. (1992) Observations on the ecology, behaviour, swimming mechanism and energetics of the of the neustonic grapsid crab, P. minutus. Journal of Marine Biological Association of the United Kingdom 72: 611-620.

Davenport, J. (1994) A cleaning association between the oceanic crab Planes minutus and the loggerhead sea turtle Caretta caretta. Journal of the Marine Biological Association of the United Kingdom 74: 735-737.

Dellinger, T., Davenport, J., Wirtz, P. (1997) Comparisons of social structure of Columbus crabs living on loggerhead sea turtles and inanimate flotsam. Journal of the Marine Biological Association of the United Kingdom 77: 185-194.

Enzenross, R., Enzenross, L. (1987) Studie über das Vorkommen von Mollusca und Crustacea an der türkischen Küste (Mittelmeer und Agäis). Ravensburg, Germany.

Frick, M.G., Kopitsky, K., Bolten, A.B., Bjorndal, K.A., Martins, H.R. (2011) Sympatry in grapsoid crabs (genera Planes and Plagusia) from olive ridley sea turtles (Lepidochelys olivacea), with descriptions of crab diets and masticatory structures. Marine Biology 158: 1699-1708.

Frick, M.G., Williams, K.L., Bolten A.B., Bjorndal K.A., Martins H. (2004) Diet and fecundity of Columbus crabs, P. minutus, associated with oceanicstage loggerhead sea turtles, Caretta caretta, and inanimate flotsam. Journal of Crustacean Biology 24: 350-355.

Holthuis, L.B., Gottlieb, E. (1958) An annotated list of the decapod Crustacea of the Mediterranean coast of Israel, with an appendix listing the Decapoda of the eastern Mediterranean. Bulletin of the Research Council of Israel 7: 1-126.

Koukouras, A., Kallianiotis, A., Vafidis, D. (1998) The decapod crustacean genera Plesionika Bate (Natantia) and Munida Leach (Anomura) in the Aegean Sea. Crustaceana 71: 714-720.

Maiorano, P., Capezzuto, F., D’onghia, G., Tursi A. (2013) Spatio-temporal changes of Munida Rutllanti Zariquiey-Alvarez, 1952 (Decapoda: Galatheidae) in the North-Western Ionian Sea (Central Mediterranean). Mediterranean Marine Science 14: 42-48.

Marco-Herrero, E., Abelló, P., Drake, P., García-Raso, J.E., González-Gordillo J.I., Guerao G., Palero F., Cuesta J.A. (2015) Annotated checklist of brachyuran crabs (Crustacea: Decapoda) of the Iberian Peninsula (SW Europe). Scientia Marina 79: 1-14.

Margaritoulis, D., Touliatou, S. (2011) Μediterranean monk seals present an ongoing threat for loggerhead sea turtles in Ζakynthos. Marine Turtle Newsletter 131: 18-23.

Melo, G.A.S. (1996) Manual de Identificação dos Brachyura (Caranguejos e Siris) do Litoral Brasileiro. São Paulo, Plêiade/ FAPESP.

Mota-Vargas, C., Rojas-Soto, O. (2012) The importance of defining the geographic distribution of species for conservation: the case of the Bearded Wood-Partridge. Journal for Nature Conservation 20: 10-17.

OBIS (2018) Ocean Biogeographic Information System. Available at: http://iobis.org (Accessed 14 Sept 2018).

Pastore, M. (1972) Decapoda Crustacea in the Gulf of Taranto and the Gulf of Catania with a discussion of a new species of Dromiidae (Decapoda Brachyoura) in the Mediterranean Sea. Thalassia Jugoslavica 8: 105-117.

Pfaller, J.B., Alfaro-Shigueto, J., Giffoni B., Ishihara, T., Mangel, J.C., Peckham, S.H., Bjorndal, K.A., Baeza, J. (2014) Social monogamy in the crab Planes major, a facultative symbiont of loggerhead sea turtles. Journal of Experimental Marine Biology and Ecology 461: 124-132.

Pfaller, J.B., Gil, M.A. (2016) Sea turtle symbiosis facilitates social monogamy in oceanic crabs via refuge size. Biology Letters 12: 20160607. DOI: 10.1098/rsbl.2016.0607.

Pollock, L.W. (1998) A Practical Guide to the Marine Animals of Northeastern North America. Rutgers University Press, New Brunswick, New Jersey & London.

Pons, M., Verdi, A., Domingo, A. (2011) The pelagic crab Planes cyaneus (Dana, 1851) (Decapoda, Brachyura, Grapsidae) in the southwestern Atlantic Ocean in association with loggerhead sea turtles buoys. Crustaceana 84: 425-434.

Rodríguez-Flores, P.C., Machordom, A., Abelló, P., Cuesta, J.A., Macpherson, E. (2019) Species delimitation and multi-locus species tree solve an old taxonomic problem for European squat lobsters of the genus Munida Leach, 1820. Marine Biodiversity DOI: 10.1007/s12526-019-00941-3.

Sainte-Marie, B. (2007) Sperm demand and allocation in decapod crustaceans. In: Evolutionary Ecology of Social and Sexual Systems: Crustaceans as Model Organisms (eds., Duffy, J.E., Thiel, M.), Oxford University Press, New York, pp. 191-210.

Spivak, E. D., Bas, C.C. (1999) First finding of the pelagic crab Planes marinus (Decapoda: Grapsidae) in the southwestern Atlantic. Journal of Crustacean Biology 19: 72-76.

Tutman, P., Kapiris, K., Kirinčić, M., Pallaoro, A. (2017) Floating marine litter as a raft for drifting voyages for Planes minutus (Crustacea: Decapoda: Grapsidae) and Liocarcinus navigator (Crustacea: Decapoda: Polybiidae). Marine Pollution Bulletin 120: 217-221.

Zariquiey-Alvarez, R. (1968) Crustáceos Decápodos Ibéricos. Investigaciòn Pesquera, Barcelona.