A. Hadj Taieb *, A. Derbali, M. Ghorbel, N. Ben Hadj Hamida, O. Jarboui

Similar documents
Feeding Habits of the Bogue, Boops boops (Linnaeus, 1758) (Teleostei: Sparidae) in Benghazi Coast, Eastern Libya

Mullus surmuletus Family Mulliadae

INTERNATIONAL JOURNAL OF BIOASSAYS ISSN: X CODEN: IJBNHY

Update of the fisheries catch reconstruction of Corsica (France), Frédéric Le Manach and Daniel Pauly

Size and spatial distribution of the blue shark, Prionace glauca, caught by Taiwanese large-scale. longline fishery in the North Pacific Ocean

Feeding Habits of Black Scorpionfish Scorpaena porcus, in the South- Eastern Black Sea

Protect Our Reefs Grant Interim Report (October 1, 2008 March 31, 2009) Principal investigators: Donald C. Behringer and Mark J.

Southern Gulf of St. Lawrence Sea Scallop

Atlantic croaker, Micropogonias undulatus (Linnaeus, 1766)

Ecological Interactions in Coastal Marine Ecosystems: Rock Lobster

Preliminary study on feeding habits and condition factor of Salmo trutta macrostigma (Dumeril, 1858) in Karasu River

West Africa Journal of Applied Ecology (WAJAE) ISSN: Volume 9 (Jan Jun 2006)

Rome, 20 February Working Group (WG1) LO. Main Outputs on Landing Obligation and Joint Recommendations by STECF

STATUS OF EXPLOITED MARINE FISHERY RESOURCES OF INDIA

Small pelagic fishery and research in Albania

Methodology for the stock assessments in the Mediterranean Sea 5-9 June 2017, (venue tbc)

V. Bukvic 2, J. Pavlicˇ evic 3, By J. Dulcˇ ic 1, P. Tutman 1, R. Grgicˇ evic 1, N. Staglicˇ ic 1, A. Pallaoro 1, S. Matic -Skoko 1, B.

FOOD OF SOME DEMERSAL FISHES FROM THE TRAWL GROUNDS OFF COCHIN. Central Marine Fisheries Research Institute,

HOW BENTHIC HABITATS AND BOTTOM TRAWLING AFFECT TRAIT COMPOSITION IN THE DIET OF EUROPEAN PLAICE (PLEURONECTES PLATESSA) IN THE NORTH SEA

Distribution and abundance of demersal fish and invertebrate fauna around the

Merlangius merlangus Family Gadidae

Diet spectrum and preference of the invasive round goby (Neogobius melanostomus) in Flanders (North Belgium)

Blue Jack mackerel (Trachurus picturatus) in Subdivision Xa2 (Azores): jaa-10_sa. June 2015 (edits made to the main text) REPLACED

Atsuko YAMAGUCHI. Since the catches of these fish decrease as the waters, including those around western Kyushu and

Last Fall I was fishing for striped bass using green crabs and sand fleas for bait but without any luck. In this presentation I will look into the

WP4 Ecosystem modelling workshop Ecopath with Ecosim

SMOOTH HAMMERHEAD SHARK (HHS)

Dietary Items and Feeding Habits of Sompat Grunt Pomadasys jubelini (Cuvier, 1830) Fatimat Adenike Adebiyi *

Assessment of feeding is an important

First occurrence of Serranus hepatus in the Bulgarian Black Sea coast

Analyse des interactions entre distributions spatiales des communautés de poisson et des flottilles de pêche

Kingfishes (whitings), Menticirrhus spp.

Abstract. The aim of this study was to determine the size and age compositions, growth

Key words: community similarity; coral patch reef; Enewetak; reeffish; species diversity; Virgin Islands.

STUDY PERFORMANCE REPORT

Relation between coral reef degradation and the Overexploitation of coral reef fishes in El-Tur region, Egyptian Red Sea Coast

Southern Gulf of St. Lawrence (4T) Herring

COUNTRY NOTE ON NATIONAL FISHERIES MANAGEMENT SYSTEMS -- SPAIN

DIET SEASONALITY AND OVERLAP OF CHRYSICHTHYS SPECIES ON LAKE KAINJI, NIGERIA

Map Showing NAFO Management Units

YELLOWFIN TUNA (Thunnus albacares)

Forage indicators and consumption profiles for Chesapeake Bay fishes

Southern Gulf of St. Lawrence (4T) Herring

AGE ESTIMATION AND GROWTH PATTERN OF THE GILTHEAD SEABREAM SPARUS AURATA (PISCES: SPARIDAE) OF THE GULF OF GABES, TUNISIA

Fishing down the marine food webs in the Hellenic seas

ASSESSMENT OF THE WEST COAST OF NEWFOUNDLAND (DIVISION 4R) HERRING STOCKS IN 2011

Small landings in small harbours

Advice June 2014

Maturity and Spawning of the Small Yellow Croaker, Larimichthys polyactis

SCHOOLING BEHAVIOR OF HAEMULON SPP. IN BERMUDA REEFS AND SEAGRASS BEDS

A study on Diet Composition and Feeding Habits of Barracuda fish (Sphyraena chrysotaenia and S. flavicauda) in the Gulf of Suez

STATUS OF EXPLOITED MARINE FISHERY RESOURCES OF INDIA

Life Beyond the Spawning Grounds: Distribution & Food Web Relations of Herring & Forage Fishes in Puget Sound

Status and trend of four commercially important coastal cephalopods in China Seas: an overview with implications for climate change

Length-Weight Relationship and Condition Factor (K constant) of Dentex maroccanus, Valenciennes 1830 (Family Sparidae) at Malindi, Kenya

AMBLYGASTER SIRM (WALBAUM) OFF THE NEGOMBO COAST

Red Sea bream in Subareas VI, VII and VIII

IOTC 2013 WPNT03 18 ABSTRACT

IOTC 2015 SC18 ES06[E]

Analysis on stomach content of bigeye tuna ( Thunnus obesus) in the eastern-central Pacific Ocean

A Combined Recruitment Index for Demersal Juvenile Cod in NAFO Divisions 3K and 3L

Current Status of Crab Fishery in the Artisanal Sector along Gulf of Mannar and Palk bay Coasts

Coastal fish nurseries: the need for a wide vision at habitat and ecological function scales

State of California The Resources.Cigency

Mackerel and Herring - Competition or Coexistence?

¹Laboratory of Vegetal Biology and Environment, University of Annaba BP 12, Annaba 2300, Algeria; hotmail.

6- Food Habits of Surf Zone Fishes

N.H. Sea Grant Research Project Post Completion Report For time period 2/1/15 1/31/16

Catch per unit effort of coastal prawn trammel net fishery in Izmir Bay, Aegean Sea

The Changes Observed in Atlantic Bonito (Sarda sarda) Populations During the Autumn-Winter Migration in the Suthern Black Sea Coast

Final report on fish diet and stomach analyses

The impact of environmental factors on fish food security in West Africa

ISSN Original Article Food and feeding habits in Leiognathus berbis (Valenciennes) from Turicorin, Southeast coast of India.

Commercial Yellowfin Tuna Fishing in the Gulf of Mexico States

Tuna [211] 86587_p211_220.indd 86587_p211_220.indd /30/04 12/30/04 4:53:37 4:53:37 PM PM

STATISTICS OF THE FRENCH PURSE SEINE FISHING FLEET TARGETING TROPICAL TUNAS IN THE INDIAN OCEAN ( )

Minute on Bangkok Meeting 3 April 2006,

North East Atlantic Fisheries Baltic Sprat Whitepaper March 2011

Predator diet as an indicator of comb jellyfish (Ctenophora) abundance dynamics in the Barents Sea

Abondance et diversité acoustique des populations de poissons dans la baie de Calvi.

Interpretation on the food and feeding habits of Dascyllus trimaculatus (Ruppell, 1829) from Gulf of Mannar, South East coast of India

.Conservation of the Fisheries of Lakes Victoria, Kyoga and Nabugabo

SC China s Annual report Part II: The Squid Jigging Fishery Gang Li, Xinjun Chen and Bilin Liu

Food habits and feeding intensity of finlet scad Atule mate (Te1eostei) off Gulf of Mannar, southeast coast of India

Co-Principal Investigators Stephen C. Jewett, Ph.D. Paul C. Rusanowski, Ph.D.

Applied policy in the Mediterranean lagoons

ASSESSMENT OF THE WEST COAST OF NEWFOUNDLAND (DIVISION 4R) HERRING STOCKS IN 2013

The fishery for jack mackerel in the Eastern Central Pacific by European trawlers in 2008 and 2009

BACHA Mahmoud 1, JEYID Ahmed 1,2, VANTREPOTTE vincent 1, DESSAILLY David 1, AMARA Rachid 1

Countermeasures against Alien Fishes (Largemouth Bass and Bluegill) in Lake Biwa

Pelagic food webs in the tropical Pacific

ADDITIONAL RECORDS AND CONFIRMED OCCURRENCE OF MEDITERRANEAN FLYINGFISH CHEILOPOGON HETERURUS (OSTEICHTHYES: EXOCETIDAE) FROM THE COAST OF TUNISIA

Prey-predator interactions between the myctophid Bentosema glaciale and calanoid copepods in the Labrador Sea

Tropical Scombrid Feeding Habits in the Central Pacific Kevin McLean S-199 June 9, 2005

Socioeconomic Characteristics of Payang Seine (Lampara) and Driftnet Fisheries in West Sumatra, Indonesia

Impacts of climate change on marine fisheries

Lionfish Dissection: Gut Content Analysis

NATIONAL BIORESOURCE DEVELOPMENT BOARD Dept. of Biotechnology Government of India, New Delhi

and found that there exist a significant overlap between the billfish resources and the exploitation activities targeting tunas and mahi mahi.

Cedar Lake Comprehensive Survey Report Steve Hogler and Steve Surendonk WDNR-Mishicot

Transcription:

Vie et milieu - Life and environment, 2013, 63 (1): 53-58 Variation of diet composition of Diplodus vulgaris (Sparidae) from the Gulf of Gabes (central Mediterranean) A. Hadj Taieb *, A. Derbali, M. Ghorbel, N. Ben Hadj Hamida, O. Jarboui Institut National des Sciences et Technologies de la Mer (Centre de Sfax) BP 1035, 3018 Sfax, Tunisie * Corresponding author: aymen.haj.82@gmail.com TROPHIC ECOLOGY TWO BANDED SEA BREAM SOUTHERN TUNISIA ABSTRACT. From March 2008 to February 2010, 2,013 two banded sea bream Diplodus vulgaris (Sparidae) ranging from 5.5 to 25.8 cm in total length (TL), fished in the Gulf of Gabes (south Tunisia, central Mediterranean Sea), were used to investigate feeding habits of the species. This study was based mainly on the variation of the index of relative importance (IRI) with respect to sex, fish size and season. Among 2,013 stomachs examined, 1,374 were empty (vacuity index: %VI = 68.26). This index (% VI) differed significantly across months and declined slightly among the seasons. A total of 22 species representing eight different families belonging to three major groups: molluscs, crustaceans, and echinoderms, were identified in stomach contents of Diplodus vulgaris. This species is primarily a generalist carnivorous fish with a diet consisting of a wide range of species. Molluscs were found in the majority of stomachs, with a total relative importance (% IRI) of 59.06 %. The Pectinids were the most important bivalve family (% IRI = 8.49), while crustaceans were the second most important food category consumed (19.07 %). There were significant differences in the diet between males and females through the seasons and between juveniles and adults. INTRODUCTION MATERIALS AND METHODS The two banded sea bream Diplodus vulgaris (Geoffroy Saint-Hiliaire, 1817) is a demersal species distributed in the Mediterranean and along the eastern Atlantic coast from France to Senegal, including the Madeira, the Azores and the Canaries Archipelagos (Bauchot & Hureau 1986, 1990). It can be found close to rocky and sandy bottoms to a maximum depth of 160 m. Juveniles often live in coastal lagoons and estuaries (Monteiro 1989) and it is considered a resident species in artificial reefs (Santos 1997). There are no reliable statistics on D. vulgaris landings on the Tunisian coasts. The entire genus Diplodus is mixed in one statistical category. Currently, this species is still abundant in the Gulf of Gabes (south of Tunisia) and it is an economically important demersal species. However, despite its abundance, very little is known about the trophic ecology of this species in the Gulf of Gabes. In the Atlantic Ocean, off the south-west coast of Portugal, Gonçalves & Erzini (1998) studied the diet of D. vulgaris. Ara (1937), Rosecchi (1987), Rosecchi & Nouaze (1987), Sala & Ballesteros (1997), Pallaoro et al. (2006) and Osman & Mahmoud (2009) studied the feeding habits of D. vulgaris in the Mediterranean Sea and Bradai et al. (1998), mainly along the Tunisian coasts, provided qualitative descriptions of the diet of D. vulgaris. The purpose of the present study was to investigate the diet and feeding habits of D. vulgaris in the Gulf of Gabes, including the effects of predator sex, size and season on stomach contents. In the Gulf of Gabes, from the parallel 35 N to the Tunisian- Libyan border (Fig. 1), Diplodus vulgaris is caught mainly by different types of artisan fishing gears (seine nets, gill nets, fyke nets); 2,013 specimens collected monthly between March 2008 and February 2010 ranging in size from 5.8 to 25.6 cm were examined fresh (1,012 males, 777 females, 40 intersexual individuals and 184 fish could not be determined macroscopically) (Table I). Immediately after capture, the total length (TL) of each fish was measured to the nearest 0.1 cm and weighed to the nearest 0.1 g. The analysis of stomach contents was made after storage in 4 % formalin. Prey were identified to the lowest possible taxon Fig. 1. Geographical position of the Gulf of Gabes (Tunisia).

54 A. HADJ TAIEB, A. DERBALI, M. GHORBEL, N. BEN HADJ HAMIDA, O. JARBOUI Table I. Sampling data of two banded sea bream Diplodus vulgaris caught from Gulf of Gabes (Tunisia), size range and % of empty stomachs (March 2008-February 2010). Month N Average Females Size range % Empty stomachs N Average Males Size range % Empty stomachs March 71 15.14 11.2-24.6 70.4 79 14.66 10.3-24 70.9 April 80 14.97 10.8-22.9 61.3 99 14.09 10.2-22.8 54.5 May 63 15.2 11.4-24.5 63.5 55 13.78 11.1-25.2 56.4 June 81 13.18 11.5-16.4 82.7 86 12.69 5.8-16.9 74.4 July 56 14.68 10-24.5 71.4 52 12.69 8.9-17.4 84.6 August 65 12.8 9.9-17.2 74.4 102 10.6 8.1-15.2 73.5 September 52 13.88 10.1-20.3 78.8 59 11.45 8.3-16.2 61 October 55 13.71 11.4-22.9 65.5 96 12.34 8.8-21.3 53.1 November 67 14.58 10-22.1 73.1 107 13 9.2-19.3 72.9 December 48 16.43 9.2-25.6 60.4 97 14.47 8.7-25.4 79.4 January 65 15.42 11.1-24.7 55.4 81 14.68 10.9-25.2 54.3 February 74 14.73 11-21.2 56.8 99 13.67 9.7-20.7 62.6 N: number of fish collected and weighed (wet) to the nearest 0.001 g. Numerous indices have been calculated to quantify the importance of different prey items in the diet of fish. Dietary descriptions of fish and other aquatic vertebrates are greatly influenced by the choice of method used to quantify the relative importance or contribution of each prey type to the diet. This is because the most commonly used methods (frequency of occurrence (% O), numerical abundance (% N) and weight estimations (% W)) convey different types of information on feeding habits (e.g., MacDonald & Green 1983, Bigg & Perez 1985, Cortés 1997). This limitation of single indices led Pinkas et al. (1971) to propose the index of relative importance (IRI) a compound index that describes the relative contribution of stomach contents to the diet. Cortés (1997) proposed to include the IRI standardized to 100% (% IRI), in addition to reporting the three single measures (% O, % N and % W), to facilitate comparisons between dietary studies. The percentage index of relative importance puts results into a common metric, more amenable for use in diet comparisons and calculation of other trophic indices. In the present study, the following indices were used: Vacuity index (% VI) = number of empty stomachs 100/total number of examined stomachs; Percentage frequency of occurrence (% O) = number of stomachs in which a food item was found 100/the total number of full stomachs; Percentage numerical abundance (% N) = number of each prey item 100/the total number of prey in all stomachs; Percentage gravimetric composition (% W) = wet weight of each prey item 100/the total wet weight of stomach contents. The main food items were determined using the index of relative importance (IRI): IRI = % O (% N + % W). This index was expressed in percentage as follows: % IRI = (IRI/ IRI 100). Prey species were sorted in decreasing order according to IRI and the cumulative %IRI was calculated and recorded for the major forage categories (Hyslop 1980) and compared among different groups according to size, season and sex. This index was examined for four size-groups that corresponded to juveniles ( 10 cm TL), sub-adults (10 < TL cm 15) and adults (15 < TL cm 20 and > 20 cm TL) of Diplodus vulgaris (Hadj Taieb et al. 2012). Statistical differences (P < 0.05) in diet composition with respect to length-class and season were assessed by the Chisquare test of the frequencies of a given prey (Sokal & Rohlf 1981). The variation in vacuity index (% VI) was also tested using the Chi-square test over a contingency table of the number of empty stomachs. RESULTS Feeding intensity Among 2,013 stomachs of Diplodus vulgaris examined, 1,374 were empty (VI% = 68.26). The proportion of empty stomachs varied significantly over the year (χ² = 40.43, P < 0.05). The highest percent of empty stomachs was found in June (82.78 %) and July (77.97 %), while the lowest was observed in January (55.56 %) (Table I). The proportion of empty stomachs was not significantly different among the two size-classes (χ² = 0.31, P > 0.05), and corresponded to juveniles (VI % = 69.73 %) and adults (VI % = 66.14 %), respectively.

FEEDING HABITS OF DIPLODUS VULGARIS 55 Diet composition Five major prey groups: molluscs, crustaceans, echinoderms, annelids and teleosts were identified in the stomach contents of Diplodus vulgaris. A total of 22 species representing 8 different families were identified. Molluscs constitute the most frequently observed group, with 59.1 % of the total % IRI, followed by crustaceans (%IRI = 19.1), while the other taxa, i.e. Spongia and Plantae were scarcely found (%IRI < 1) (Table II) and for this reason are not indicated in all figures. At the family level, Pectinidae was the major prey consumed by D. vulgaris (% IRI = 8.5), followed by Nereidae (Nereis sp.) (% IRI = 4.3) and Sepiidae (% IRI = 3.6) (Table II). Diet composition in relation to sex Overall, molluscs had a higher percentage of IRI than crustaceans. The % IRI of molluscs and crustaceans in female two banded sea bream (67.3 % and 15.4 %, respec- Table II. Diet composition of Diplodus vulgaris of the Gulf of Gabes (Tunisia). Group Family Item (species) O% N% W% IRI IRI% Crustaceans Isopoda Cymodoce truncata 1.88 2.67 1.23 7.32 0.2 Sphaeroma sp. 2.5 3.74 1.94 14.21 0.3 Gammaridae Ampelisca diadema 1.1 0.8 0.97 1.94 0.04 Panaeidae Metapenaeus monoceros 0.47 0.36 0.31 0.31 0.007 Trachysalambria curvirostris 1.1 0.89 1.19 2.28 0.05 Processidae Processa edulis 1.41 1.25 1.02 3.19 0.07 Non-identified shrimps 2.66 2.05 2.55 12.23 0.3 Carididae Carcinus maenas 3.6 3.02 3.57 23.73 0.5 Majidae Macropodia longirostris 1.41 1.16 1.71 4.04 0.09 Amphipoda Gen. Sp. 3.29 3.56 2.98 21.5 0.5 Non-identified crustaceans 1.72 0.98 0.6 2.72 0.06 Total crustaceans 21.6 20.91 18.34 847.66 19.1 Molluscs Pectinidae Pecten jacobaeus 4.85 7.3 3.72 53.45 1.2 Flexopecten glaber 1.72 2.49 2.26 8.18 0.2 Chlamys sp. 5.32 9.79 5.48 81.21 1.8 Cardiidae Cerastoderma glaucum 1.56 2.05 2.14 6.55 0.1 Non-identified Bivalvia 10.33 6.85 5.23 124.81 2.8 Cerithiidae Cerithium scabridium 1.41 2.4 0.74 4.42 0.1 Bullidae Bulla striata 1.1 0.89 0.71 1.75 0.04 Non-identified Gastropoda 0.94 0.53 1.55 1.95 0.04 Sepiidae Sepia officinalis 8.45 5.25 13.65 159.75 3.6 Total molluscs 35.37 38.43 35.81 2625.92 59.1 Echinoderms Echinoidea 2.35 1.87 1.88 8.79 0.2 Hotoloroidea 1.72 1.07 0.9 3.39 0.08 Ophiuroidea 8.29 6.32 6.17 103.59 2.3 Total echinoderms 12.52 9.43 9.03 231.1 5.2 Teleosts Clupeidae Sardinella aurita, Sardina pilchardus 2.35 1.96 7.04 21.12 0.5 Engraulidae Engraulis encrasicolus 1.41 1.07 3.92 7.03 0.2 Gobiidae Gobius niger 1.1 0.71 2.45 3.47 0.08 Mullidae Mullus surmuletus 1.25 0.89 1.72 3.27 0.07 Non-identified Teleosts 0.78 0.44 0.34 0.62 0.01 Total teleosts 7.2 5.34 17.21 162.32 3.7 Annelids Nereidae Nereis sp. 9.86 11.3 8.31 193.36 4.3 Spongia 5.01 2.94 1.58 22.62 0.5 Tunicate Ascidiacea 1.72 1.07 0.92 3.42 0.08 Plantae 4.07 2.49 1.63 16.79 0.4 Non-identified 9.23 5.25 3.37 79.62 1.8

56 A. HADJ TAIEB, A. DERBALI, M. GHORBEL, N. BEN HADJ HAMIDA, O. JARBOUI Fig. 2. Diet composition of Diplodus vulgaris in the Gulf of Gabes for males and females, based on the percentage index of relative importance values of the major prey groups: n = number of non-empty stomachs analysed in each sex. crustaceans was comparatively low (% IRI = 2.5). The frequency of crustaceans significantly decreased with increasing size (χ² = 8.2, P < 0.05). Annelids occurred in stomachs of specimens belonging to medium size-class (sub-adults, 10 < TL cm 15). In the large size-class (adults, > 20 cm TL) molluscs represented more than 78 % of the total IRI. Significant differences among size-classes were found for molluscs (χ² = 16.2, P < 0.05), crustaceans (χ² = 8.2, P < 0.05), echinoderms (χ² = 11.7, P < 0.05) and annelids (χ² = 40.2, P < 0.05). Diet composition in relation to season There were some seasonal variations in food habits of D. vulgaris (Fig. 4). Molluscs were the dominant prey group during the seasons. Crustaceans were also present in the stomachs throughout the year, with a peak value recorded in autumn (% IRI = 29.7). Echinoderms were found in winter, autumn and spring. Significant differences among seasons were found for the major prey groups (molluscs: χ² = 29.1, P < 0.05; crustaceans: χ² = 14.9, P < 0.05; echinoderms: χ² = 9.3, P < 0.05; annelids: χ² = 10.5, P < 0.05 and fishes: χ² = 13.6, P < 0.05). Fig. 3. Diet composition of Diplodus vulgaris in the Gulf of Gabes among size-classes, based on the percentage index of the relative importance values of the major prey groups: n = number of non-empty stomachs analysed in each size-class. Fig. 4. Diet composition of Diplodus vulgaris in the Gulf of Gabes throughout the year based on the percentage index of relative importance values of the major prey group: n = number of non-empty stomachs analysed in each season. tively) were similar to that observed in males (63.4 % and 15.1 %, respectively). There were appreciable dietary differences between males and females in prey categories of annelids (χ² = 13.5, P < 0.05) (Fig. 2). Diet composition in relation to fish size Molluscs and crustaceans were the major prey groups present in the diet of all size-classes (Fig. 3). Molluscs were the most important prey group in the large size-class (> 20 cm TL) (% IRI = 78.6), while the contribution of DISCUSSION Dietary studies of Diplodus vulgaris in the Gulf of Gabes, central Mediterranean, show a high proportion of empty stomachs and few prey items per stomach, most of them in advanced stages of digestion. Bradai et al. (1998) reported that the percentage was higher than 88 % on the Tunisian coasts, but it was less than 19 % in the eastern Adriatic Sea (Pallaoro et al. 2006). The high %VI may be related to the fact that captures occurred at night, which is when the fish are most active generally because they are feeding. The individuals caught were hauled onboard the following morning, so some of them may have remained in the net for several hours, and their capture may have occurred before the ingestion of prey or after digestion. As a result, many specimens had an empty stomach at the moment they were collected. Our study indicates that Diplodus vulgaris is a generalist predator that consumes a wide range of prey items. It is mainly a mollusc-based carnivorous species, as are most of the species of the genus Diplodus (Rosecchi 1987, Bradai 2000, Osman & Mahmoud 2009). Its most common prey groups, which represent 59.1 % or more of the total IRI, can be considered as the main food. The other prey groups (i.e. echinoderms, teleosts and annelids) were of minor importance and may be considered as occasional food. The common cuttlefish Sepia officinalis and the Pectinid Pecten jacobeus have the highest index of relative importance in the diet of D. vulgaris. Penaeidae (i.e.

FEEDING HABITS OF DIPLODUS VULGARIS 57 Metapenaeus monoceros and Trachypenaeus curvurostris), Isopoda (i.e. Cymodoce truncata) and Clupeidae (Sardinella aurita and Sardina pilchardus) were of secondary importance. Nevertheless in the east Adriatic, D. vulgaris is an opportunistic predator species and feeds primarily on echinoids (Pallaoro et al. 2006). The feeding patterns of Diplodus vulgaris observed in the present study agree well with field distribution patterns of several mollusc species. For example, the Pectinid Pecten jacobaeus, commonly present in Tunisian waters (Zamouri Langar et al. 2011, El Lakhrach et al. 2012), especially in the Gulf of Gabes, was frequently found in the stomachs of this species, whereas, the other molluscs: Cerastoderma glaucum, Pinctada radiata and Cerithium scabridium were less frequently encountered. Diet often changes with geographical area and this was observed for D. vulgaris as well. In the Gulf of Gabes, D. vulgaris seems to have a diet different from that of other areas, with few similarities. In the Atlantic Ocean (Gonçalves & Erzini 1998), the primary food of this species consists mainly of a wide range of small prey which are often very frequent (polychaetes, ophiuroids, amphipods) with large prey being rare (cephalopods). Bradai et al. (1998) also reported that molluscs, crustaceans and echinoderms were present in the stomach contents in the same area. Taken together, the results of these studies confirm the importance of molluscs and crustaceans in the diet of D. vulgaris. Rosecchi (1987) reported that D. vulgaris from the Gulf of Lions is mainly a carnivorous fish. The observed variations suggest that the diet composition of D. vulgaris may be greatly modified in response to the availability of prey and/or different benthic faunal communities in the two areas. Ara (1937) in Naples (Italy) and Quéro (1984) in France reported that the two banded sea bream was a generalist feeder, with crustaceans and molluscs forming the basis of the diet. Bauchot & Hureau (1986) considered this a carnivorous species, feeding mainly on crustaceans, molluscs, and worms. These authors did not attribute much importance to echinoderms and polychaetes, which may be due to regional differences in faunal composition, given the lack of information on feeding selectivity in these studies. In comparison to other Sparidae, the diet of Diplodus vulgaris in the Gulf of Gabes most closely resembles that of Spondyliosoma cantharus (Bradai et al. 1998), both species feeding on molluscs and crustaceans. However, the diet of the Sharpsnout sea bream, Diplodus puntazzo, from the Tunisian coasts (Bradai et al. 1998) and the eastern central Adriatic Sea (Dulčić et al. 2006) were mainly zooplanktonic crustaceans, while Spongids were of minor importance. In this study, the obtained results show that food habits considerably change as fish grow. While the juveniles had a higher proportion of crustaceans in their diet than adults, molluscs were still the dominant prey group for all size classes. Juveniles tended to consume a less diverse range of prey species, comprising mostly zooplanktonic crustaceans (larvae of shrimps, Isopoda and Gammaridae), Annelids and small pelagic fish and fish larvae. Larger specimens appear to become more piscivorous and therefore capable of capturing large teleosts that have a high percentage of stomach content weight. These differences could be attributed to the size of the specimens. Adults of D. vulgaris have diets comprising mostly molluscs, teleosts and crustaceans. In our study, the stomach contents of D. vulgaris showed seasonal variations, but molluscs were the dominant prey group during all seasons. Crustaceans were also present in the stomachs throughout the year, with a peak value recorded in autumn. Echinoderms were found in winter, autumn and spring. In conclusion, D. vulgaris is mainly a carnivorous fish. The diet in the Gulf of Gabes as well as in the north-east Atlantic waters consists mainly of molluscs and crustaceans. The importance of molluscs differed significantly among seasons as well as between small and large sizeclasses. The feeding activity of this species throughout the year was probably related to fish abundance and seawater temperature and spawning period. Future monitoring of the Gulf of Gabes feeding ecology of D. vulgaris could help us better understand the inter- and intra-specific interactions that occur in this region, and how climate change, overexploitation and pollution affect these interactions. Ack n o w l e d g e m e n t s. Special thanks to the technical and supporting staff of INSTM (Centre de Sfax) for their practical assistance in laboratory analysis. We thank N Kallel, an English teacher at the Faculty of Sciences (Sfax), for proof-reading our manuscript. The authors are also grateful to the anonymous referees whose suggestions and comments improved the submitted manuscript. REFERENCES Ara L 1937. Contributo allo studio dell alimentazione dei pesci: Sargus vulgaris Geoffr, - Sargus annularis L. Sargus sargus L. Boll Pesca Piscicolt Idrobiol 13(4): 371-381. Bauchot ML, Hureau JC 1986. Sparidae. In Whitehead PJP, Bauchot, ML, Hureau JC, Nielsen J, Tortonese E (eds), Fishes of the North-Eastern Atlantic and the Mediterranean II. UNESCO, Paris: 883-907. Bauchot ML, Hureau JC 1990. Sparidae. In Quero JC, Hureau JC, Karrer C, Post A, Saldanha L (eds), Checklist of the fishes of the eastern tropical Atlantic (CLOFETA). JNICT, Lisbon; SEI, Paris, and UNESCO, Paris, 2: 790-812. Bigg MA, Perez MA 1985. Modified volume: a frequency-volume method to assess marine mammal food habits. In Beddington JR et al. (eds), Marine mammals and fisheries. London: George Allen & Unwin: 277-283.

58 A. HADJ TAIEB, A. DERBALI, M. GHORBEL, N. BEN HADJ HAMIDA, O. JARBOUI Bradai MN 2000. Diversité du peuplement ichtyque et contribution à la connaissance des sparidés du golfe de Gabès. Thèse Doctorat d État. Faculté des Sciences de Sfax, 595 p. Bradai MN, Ghorbel M, Jarboui O, Bouain A 1998. Régime alimentaire de Spondyliosoma cantharus, Diplodus puntazzo, et D. vulgaris (Teleostei, Sparidae) dans le golfe de Gabès, Tunisie. Rapp Comm Int Mer Médit 35: 380-381. Cortés E 1997. A critical review of methods of studying fish feeding based on analysis of stomach contents: application to elasmobranch fishes. Can J Fish Aquat Sci 54: 726-738. Dulčić J, Lipej L, Glamuzina B, Bartulović V 2006. Diet of Spondyliosoma cantharus and Diplodus puntazzo (Sparidae) in the Eastern Central Adriatic. Cybium 30(2): 115-122. El Lakhrach H, Hattour A, Jarboui O, Elhasni K, Ramos-Espla AA 2012. Spatial distribution and abundance of the megabenthic fauna community in Gabes Gulf (Tunisia, eastern Mediterranean Sea). Medit Mar Sci 13(1): 12-29. Gonçalves JMS, Erzini K 1998. Feeding habits of the two-banded sea bream (Diplodus vulgaris) and the black sea bream (Spondyliosoma cantharus) (Sparidae) from the south-west coast of Portugal. Cybium 22(3): 245-254. Hadj Taieb A, Ghorbel M, Hadj Hamida N, Jarboui O 2012. Reproductive biology of Diplodus vulgaris (Teleostei, Sparidae) in Southern Tunisian waters (Central Mediterranean). Acta Adriat 53(3): 437-446. Hyslop EJ 1980. Stomach contents analysis - a review of methods and their application. J Fish Biol 17: 411-429. MacDonald JS, Green RH 1983. Redundancy of variables used to describe importance of prey species in fish diets. Can J Fish Aquat Sci 40: 635-637. Monteiro P 1989. La faune ichtyologique de la lagune Ria Formosa (Sud Portugal). Répartition et organisation spatio-temporelle des communautés : application à l aménagement des ressources. Thèse Doctorat, Univ Sciences et Techniques du Languedoc, Montpellier: 219 p. Osman AM, Mahmoud HH 2009. Feeding Biology of Diplodus sargus and Diplodus vulgaris (Teleostei, Sparidae) in Egyptian Mediterranean Waters. World J Fish Mar Sci 1(4): 290-296. Pallaoro A, Santic M, Jardas I 2006. Feeding habits of the common two-banded sea bream, Diplodus vulgaris (Sparidae), in the eastern Adriatic Sea. Cybium 30(1): 19-25. Pinkas L, Oliphant MS, Iverson ILK 1971. Food habits of albacore, bluefin tuna and bonito in California waters. Fish Bull 152: 1-105. Quéro J C 1984. Les Poissons de mer des pêches françaises. Jacques Grancher, Paris: 394 p. Rosecchi E 1987. L alimentation de Diplodus annularis, Diplodus sargus, Diplodus vulgaris et Sparus aurata (Pisces, Sparidae) dans le golfe du Lion et les lagunes littorales. Rev Inst Pêches Marit 49(3-4): 125-141. Rosecchi E, Nouaze Y 1987. Comparaison de cinq indices alimentaires utilisés dans l analyse des contenus stomacaux. Rev Inst Pêches Marit 49(3-4): 111-123. Sala E, Ballesteros E, 1997. Partitioning of space and food resources by three fish of the genus Diplodus (Sparidae) in a Mediterranean rocky infralittoral ecosystem. Mar Ecol Prog Ser 152: 273-283. Santos MN 1997. Ichthyofauna of the artificial reefs of the Algarve coast. Exploitation strategies and management of local fisheries. PhD Thesis, Univ Algarve, UCTRA, Faro: 223. Sokal RR, Rohlf FJ 1981. Biometry. San Francisco. WH Freeman, USA: 859. Zamouri Langar N, Chouba L, Ajjabi Chebil L, Mrabet R, El Abed A 2011. Les coquillages bivalves des côtes tunisiennes. Institut national des sciences et technologies de la mer, Tunisie d imprimerie Papeterie (TIP): 128. Received August 2, 2012 Accepted April 30, 2013 Associate Editor: T Changeux