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Food of Cobia, Rachycentron canadum, from the Northcentral Gulf of Mexico PDF

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Preview Food of Cobia, Rachycentron canadum, from the Northcentral Gulf of Mexico

GulfRescaichReports,Vol.9.No.3,161-167,1996 ManuscriptreceivedAugust23.1995;acceptedSeptember18,1S>95 FOOD OF COBIA,RACHYCENTRONCANADUM, FROM THE NORTHCENTRAL GULF OF MEXICO GabrieleH.Meyer*andJamesS.Franks^ ^UniversityofSouthernMississippi.DepartmentofBiologicalSciences, Box5018,Hattiesburg,MS39406-5018,USA ^GuifCoa^ResearchLaboratory,P.O.Box7000,Oceanbrings,Mississippi39566-7000,USA AB^RACT Thestomachcontentsof403cobLa,Rachycentroncanadum,caughtinthenorthcentralGulfof Mexicorecreational fishery from April throughOctoberof1987-1990wereexamined. Cobiaranged from 373-1,530mminforklength. Ofthe403stomachs,287(71.2%)containedatleastoneidentifiableprey taxon. Crustaceans,consisting{uimarilyofpoTtunidcrabs,werethepredominantfood. Crustaceansoccurredin 79.1%ofthestomachsandcomprised77.6%ofthetotalnumberofidentifiableprey. Thesecondmostimportant preycategorywasfishwhichwasdominatedbyhardheadcatfish,Ariasfelis,andeels. Fishoccurredin58.5% ofthestomachsbutonlyaccountedfor20.3%ofthetotalnumberofprey.Theimportanceoffishaspreyincreased withincreasingsize(length)ofcobia,withthelargestsizeclassofcobia(1,150-1,530mmFL)showingthehighest percentfrequencyoccurrenceoffishprey(84.4%).Therewerenosignificantdifferencesbetweenthedietsofmale andfemalecobia. Speciescompositionofthedietindicatedthatcobiaexaminedinthisstudyweregeneralist carnivoresintheirfeedinghabitsandfedprimarilyonbenthic/epibenthiccrustaceansandfishes. However,the occurrenceofpelagicpreyprovidedevidenceofdiversityintheforagingbehaviorofcobia. Feedingincobia indicatedtheirdependenceuponpreyavailabilityratherthanuponafewspecificfoodorganisms. Introduction Theseresearchersfoundthatcrustaceansandfishmadeupthe dietofR.canadum,althoughtheirconclusionsvariedonthe Rachycentron canadum,commonlyknownascobia relativeimportanceofeachpreytype. orling,isawidelydistributed,pelagicfishwhichoccurs Knowledgeofthefoodhabitsofcobiaisnecessaryfor worldwideintropical,subtropical,andwarm temperate understandingtheroleofdietintheirgrowthandsurvival seas, except in the central and eastern Pacific Ocean andforcomprehendingthedynamicsofthefishery. The (ShafferandNakamura1989),InthewesternAtlantic,the purposeofthisstudywastodescribethedietofcobiafrom cobia occurs from Massachusetts to Argentina (Briggs thenorthcentralGulfofMexico. 1958),butismostcommonin!heGulfofMexico(Migdalski and Fichter 1983), where it supports an important MaterialsandMethods recreationalfishery. IntheGulfofMexico(Gulf)cobia rangefromKeyWest,FloridaalongthecoasttoCampeche, Mexico(Dawson 1971). Cobiatypicallymigrateduring Cobiaexaminedinthisstudywerecaughtbyhook-and-line spring and summer from their wintering grounds off inthenorthcentralGulfrecreationalfisheryfromAprilihrou^ southern Florida to spawning/feeding grounds in the Octoberof1987-1990.CobiaweretakenoffsoulheastLouisiana, northernGulfandreturntotheirwinteringgroundsinlate Mississippi,Alabama,andnorthwestFloridabetween fallandearlywinter(BiesiotetaL1994,Franksetal,1991). lat. 30^.0'-29’^.(yN and long. 86^-89^0.0^, The The diet ofR. canadum from the GulfofMexico, majorityofspecimensweretakenoffcoastalMississii^i.Some particularlythenorthernGulf,ispoorlyknown. Mostof fishwereprovidedbystateandfederalfisheriesagencies. thepreviousresearchonthefeedinghabitsofcobiawas Fish were well-iced from the time of capture until limitedtosimpledescriptionsofpreyitemsfoundinafew Stomachswereremovedatfishingdocksorcoastalfishing mm stomachs. Miles(1949)reportedthestomachcontentsof tournaments. Forklength(FL)wasmeasuredin and 11 cobia from Aransas Bay, Texas, and Knapp (1949, the sex was recorded. Most stomachs were placed in 1951)notedthepreyfoundin24cobiatakenfromthesame sealableplasticbagsandstoredinaniceslurryforshort- area. Reid(1954),Boschung(1957),andChristmasetal, term storage, usually 4-6h. Stomachs were then either (1974)commentedonfeedinginasmallnumberofcobia frozen or placed in 10% buffered formalin for later fromCedarKey,Florida(onefish),coastalAlabama(four examination.Occasioiudly,whentimepermitted,stomachs fish)andoffshoreMississippi(elevenfish),respectively. wereremovedfromfish,opened,andprocessedinthefield. 161 MeyerANDFranks Stomachs were thawed or removed &om fornialin, compared. Acontingencytableanalysisandpost-hoctest opened, and scored as either containing foodorempty. (Freeman-Tukeytransformation)forproportionaldatawere Stomachcontentsweregentlyrinsedwithfreshwaterinto usedtodeterminesignificantdifferences(«=fi.05)between a0.5mmmeshsieve.I^yitemswereseparated,identified classesforeachmajorpreycategory(Zar 1984). to the lowest possible taxon, and counted. Accurate Major prey of male and female cobia were also identificationandcountscouldbemadeinmostcasessince compared. Sincemalestendedtobesmallerthanfemales, foodsweregenerallyswallowedwhole. Somepreyitems onlycobiawithinthesizerange590-1,045mmFLwere were in advanced stages ofdigestion and could not be selected. TTiisrangecontainedmostofthemalessampled identified to species; however, those prey were often and reduced the confounding effect of size. Tests for identifiabletothefamilyororderlevel. significantdifferences(«=0.05)weremadeusingaFisher exacttestcorrectedforcontinuity. Analyses All analyses were based on stomachs containing at Results least one identifiable taxon. Prey loo far digested for identification were not used in any computations. The stomach contents of403R. canadum, ranging Additionally,someitemsfoundinstomachswereexcluded from373-1,530mmFL,wereexamined.Ofthesestomachs, becausetheywereprobaWyingestedincidentaUy.Examples 287(71.2%)containedatleastoneidentifiablepreytaxon. oftheseweretubesofChaetopteruswonns,fragmentsof Prey consisted of crustaceans, fishes, and cephalopods bivalveandgastropodshells,Sarga&sumweed,andpieces (Table 1). Another 35 (8.7%) stomachs containedonly of coral, wood, and leather. Parasitic nematodes and badlydecomposed,unidentifiableremains.Theremaining acanthocephalonswhichoccurredinsomeofthestomachs 81 stomachs(20.1%)wereempty. werealsonotconsideredinthedietanalyses. Numeric abundance, frequency of occurrence and Invertebrates percentfrequencyofoccurrence(%F)weretabulatedforall identifiable prey. In addition, major prey categories Crustaceans were the iMiraary food of cobia and, (crustaceans, fish, and cephalopods) were analyzed for essentially,dominatedthediet. Crustaceansoccurredin percentnumericabundance(%N)andpercentfrequencyof 79.1%ofthestomachsandrankedfirst(77.6%)innumeric occurrence. importance among prey (Figure 1). Crustaceans were Threedifferentforklengthsizeclassesofcobia,small representedbyeightfamiliesofdecapodsandtwofamilies (373-945 mm), medium (950-1,145 mm), and large ofstomatopods(Table1). (1,150-1,530mm), wereselectedbased onnaturalbreaks Portunid crabs werenotonly the predominant taxa within the size frequency distribution, and the percent among invertebrates consumed (Table 1) but also firequency ofoccurrence ofmajorprey within each was represented 60.7%N oftotal food items in the diet and occurredin72.8%ofthestomachs. Thelesserbluecrab, Callinectessimilii, was themostabundantprey species foundin the diet, comprising 36.5%N andoccurring in 48.8% ofthe stomachs. The iridescentswimmingcrab, Portunusgibbesih (12.5%N,26.5%F) and the ladycrab, Ovalipesfloridanus,(9.0%N,23.3%F)werethenextmost importantfoodsinthediet. Following the portunids in importance were the sicyoniids and penaeids (combmed=9.6%N). Other decqxxls, ).e.,calllanassids. calappids,majids,pagurids andxanthids,occunedinfiequeittly(Table1).Stomatopods, predominantlySquUlidae,comprised6.9%Nofthediet. Cephalopodscomprisedtheotherprimaryinvertebrate CfU3taco«na Fish Cephatopods prey group and were represented by two families, Figure 1, Percentnumericabundance(%N)andpercent LoUginidae, the predominant group, and Octopodidae. frequencyofoccurrence(%F)ofmajorpreycategoriesof Cephalopodswerefoundin13.2%ofthestomachsbutonly RachycenirancanadumtromthenorthcentralGulfofMexico. madeup2.2%Nofpreyconsumed(Figure 1). 162 FoodofCobiafromNorthcentralGulfofMexico TABLE 1 Preyitemsoccurringinstomachsofcobia,Rachycentroncanadum^ffomthenorthcentralGulfofMexico,1987-90. PercentfrequencyofoccurrencebasedonN=2S7, Totalnumb^ Frequencyof Percentfrequency Prey ofindividual occurrence ofoccurrence preyitems INVERTEBRATES Crustaceans Decapoda Pcnaeidae Penaeusaztecus 3 1 0.3 Penaeussetiferus 1 1 0.3 Penaeussp- 34 8 2.8 Trachypenaeussp. 37 9 3.1 Sicyoniidae Sicyoniabrevirostris 62 15 5.2 Sicyoniasp. 102 18 6.3 Callianassidae Callichirusislagrande 1 1 0.3 Paguridaesp. 2 2 0.7 Calappidae Calappaflammea 2 1 0.3 Hepatusepheliticus 2 2 0.7 Majidae Libiniaemarginata 1 1 0.3 Portunidac Arenaeuscribrarius 16 8 2.8 Callinectessapidus 5 5 1.7 Callinectessimilis 909 140 48.8 Ovalipesfloridanus 224 67 23.3 Portunusgibbesii 312 76 26.5 Portunussayi 1 1 0.3 Portunusspinicarpus 16 3 1.0 Portunusspinimanus 30 17 5.9 Xanthidae Menippeadina 1 1 0.3 Stomatopoda Lysiosquillidae Lysiosquillascabricauda 2 2 0.7 Squillidae Squillachydaea 2 2 0.7 Squillaempusa 78 21 7.3 Squitlaneglecta 1 1 0.3 Squillasp. 88 40 13.9 Cephalopods Loliginidae Lotigopealei 1 1 0.3 Unid.loUginids 47 33 11.5 Octopodidae Octopussp. 6 4 1.4 FISH Squatinidae Squatinadumeril 1 1 0.3 Dasyaddae Dasyatissp. 7 7 2.4 Torpedinidae t^arcinebrasiliensis 4 3 1.0 Anguillifonnes 133 52 18.1 163 MeyerANDFranks Totalnumber Fi^equencyof Percentfrequency Prey ofmdividual occurrence ofoccurrence preyitems Clupeidae Brevoortiapatronus 19 3 1.0 Brevoortiasp. 2 2 0.7 Unid.clupeids 4 4 1.4 EngrauUdae Anchoasp. 2 1 0.3 Unid.engraulid 1 1 0.3 Axiidae Ariasfelis 138 70 24.4 Ophidiidae 5 4 1.4 Ogcocephalidae Halieuiichthysaculeatus 1 1 0.3 Syngnatliidae 2 2 0.7 Triglidae Prionotussp. 48 7 2.4 Serranidae Diplectrumbivitatum 33 2 0.7 Unid.serranids 2 1 0.3 Carangidae Decapteruspunctatus 26 18 6.3 Serioladumerili 1 1 0.3 Unid.carangid 1 1 0.3 Lutjanidae Latjanuscampechanus 3 3 1.0 Sparidae Lagodonrhomboides 10 10 3.5 Unid.sparid 1 1 0.3 Sciaenidae Menticirrhussp. 3 3 1.0 Micropogoniasundulatus 9 3 1.0 Cynoscionsp. 1 1 0.3 Lehstomusxamhurus 1 1 0.3 Mugilidae Mugilsp. 5 3 1.0 Uranoscopidae Astroscopusy-graecum 5 5 1.7 Trichiuridae Trichiuruslepturus 3 1 0.3 Stromateidae Peprilusburti 1 1 0.3 Peprilussp. 3 1 0.3 Bothidae Citharichthyssp. 12 3 1.0 Etropuscrossotus 1 1 0.3 Etropussp. 2 1 0.3 Soleidae Symphurusplagiusa 1 1 0.3 Symphurussp. 1 1 0.3 Balistidae Batistescapriscus 1 1 0.3 Unid.balistids 4 3 1.0 Tetiaodontidae Chilomycterusschoepfi 2 2 0.7 Unid.tctraodontids 6 3 1.0 Total 2,491 Numberofstomachsexamined 403 Number(and%)ofstomachscontainingidentifiableprey 287 (71.2) Number(and%)ofstomachscontainingonlydecomposed,unidentifiableremains 35 (8.7) Number(and%)ofemptystomachs 81 (20.1) 164 FoodofCobiafromNorthcentralGulfofMexico Fish Incontrast,theimportanceoffishaspreyincreased withincreasingsizeofcobia.thelargestsizeclassshowing AlthoughcontributingsubstantiaUytothediversityof thehighestpercentfrequencyofoccurrence (84.4%) thediet,fishwerenotasimportantascrustaceans. Fish occurred in 58.5% of the stomachs and accounted for (Figure2). Theincreaseinfishoccuirencewasattributable 20.3%Nofallpreyconsumed(Figure1). Awidevariety tothehard-headcatfish,Ariusfelis,whichincreasedfrom offisheswasconsumed,includingtwentyfamiliesofbony 7.0%Finthesmallsizeclassto43.8%Finthelargecobia fishesandthreefamiliesofcartilaginousfishes(Table1). (Table2). Again,con^gency table analysis(x^27.77, The hardhead catfish. Ariusfelis, and eels (Order df=2,/kO.001)andpost-hoctests indicated that all size Anguilliformes)werebyfarthepredominantfishesinthe classesweresignificantlydifferentfromeachother. diet.Ariusfetis^foundin24.4%ofstomachs,exhibitedthe Thepercentageofcephalopods(predominantlysquid) highest numeric percentage (273%) among fish and remained consistently low across the three size classes contributed5.5%NtothetotaldietEelsoccurredin18,1% (Figure2,Table2). Nosignificantdifferenceswerefound. ofstomachs, comprised 26.3%N offish inthe diet,and accountedfor5.3%Noftotalitemsinthediet. Comparisonofthedietsofmaleandfemalecobia Fishlessfrequentlyencounteredinthedietincluded roundscad,£>ecupre/‘U5puncraruj(Carangidae)andpmfish, Ihedietofmaleandfemalecobiawithinthesizerangeof Lagodon rhomboides (Sparidae). Other identified fish 59()-l,045inmFLappearedtobesimilar(Table3).Crustaceans occurredonlyrarely(Table 1). were the dominantprey in both sexes. Althoughfemales showedahigherpercentfrequencyofoccurrence(86.8%)of Comparisonofdietamongsizeclassesofcobia crustaceansihandidmales(79.2%),thesedifferenceswerenot Crustaceansdominatedthedietofthesmall(77.2%F) significant, Portunid crabs were themajor componentof andmedium(84.8%F)sizeclassesofcobia,andmadeup crustaceansingestedbybothsexes. aprimaryportion(65.6%F)ofthelargesizeclass(Figure2). Fish occurred with greater frequency in the dietof Despitethesehighfrequencies,contingencytableanalysis males (60.4%F) than in the diet of females (46.2%F), (x^10.25,df=2,p<0.05)andthecorrespondingpost-hoc partiallyduetoagreateroccurrenceofeelsinthemalediet tests indicated all three size classes were significantly (Table3). Males,however,fedlessfrequentlyoncatfish. different from each other. Portunid crabs, particularly Aswiththecrustaceanprey,nosignificantdifferenceswere CalUnectessiwi/is,werethemostimportantpreyconsumed found betweenthediets ofmale and female cobia with inallsizeclassesofcobia(Table2). respecttofishorcephalopodprey. TABLE! TABLES Percentfrequencyofoccurrenceofmajortaxainthestomachs IN^rcentft^uencyofoccurrenceofm^jortaxafromthestomachs of three size classes ofRachycentron canadum from the ofmaleandfrmaleRorhycenl^oncanadumfromthenorthcentral northcentralGulfofMexico. GulfofMexico. Sizerangefrom590-1045mmFL. Male Female Forklength(mm) 373-945 950-1145 1150-1530 iV=48 N=106 N==57 N=164 N=64 Crustaceans Crustaceans (AllCrustaceans) (79.2) (86.8) (Portunidcrabs) (63.2) (80.5) (64.1) (Portunidcrabs) (70.8) (80.2) CalUnectessimilis 35.1 53.0 51.6 CalUnectessimilis 33.3 52.8 Portunusgibbesii 17.5 31.1 23.4 Portunusgibbesii 20.8 32.1 Ovalipesfloridanus 16.7 30.2 Ovalipesfloridanus 19,3 28.0 15.6 Stomatopods 14.6 19.8 Stomatopods 24.6 19.5 25.0 Fish Fish (AllFish) (60.4) (46.2) Anguilliformes 14.0 19.5 18.8 Anguilliformes 27.1 17.9 Ariusfelis 7.0 22.0 43.8 Ariusfelis 6.3 17.0 Cephalopods Cephalopods Loliginidae 17.5 9.1 14.1 Loliginidae 10.4 14.2 165 , MeyerANDFranks Discussion Wefoundcrustaceans,primarilyportunidcrabs,tobe the dominant foods ofcobiaboth in terms ofnumeric abundanceandpercentfrequencyofoccurrence. Fishes weresecondinorderofimportance. Theseresultsvary somewhatfromthefindingsofotherresearchers. Miles (1949)reportedcrabs,shrimps,andfishesinnearequal numbersinthestomachsofcobiatakenfromAransasBay Texas,and,similarly,diristmasetal,(1974)foundthe numbersoffishesandcrustaceanstobeapproximatelythe same in their samples from northern Gulf waters off Mississippi. Insharpcontrast,Knapp(1951)observeda Forkler\gth(mm) predominanceoffishes(83.3%F),followedbystomatopods (58%F),penaeidshrimps(46%F)andcrabs(42%F)inthe Figure 2. Percent frequency ofoccurrence ofmajor prey categories for three size classes ofRachycentron canadum diet of cobia caught near Aransas Bay. Texas. The fromthenorthcentralGulfofMexico. conclusions reached in previous studies werebasedon examinationsofalimitednumber(24orless)ofstomachs. Althoughcobiaexaminedinourstudywerecollectedby epibenthic crustaceans and fishes, although some hook-and-lineand,therefore,didnotrepresentarandom feedingdidoccurinthewatercolumnandnearsurface. sample,webelieveourfindingsrepresentamorcdefinitive Additionally,ourresultsindicate thatthecobiaisan descriptionofthedietofcobiainthenorthernGulfof opportunistic carnivore and that feeding appears to Mexico,due,inpart,toourhighsamplenumber(7V=287) depend more on prey availability rather than upon a andextensivegeographicalrange. few specific food organisms. Althoughcrustaceans were thedominant food, our resultsalsoindicatedthatlargercobia,malesandfemales Acknowledgments alike,consumedfishwithsignificantlygreaterfrequency thandidsmallercobia.Thismayreflectanontogenetic shifttoward fish as prey in largercobia. Our results, WethankTomMcllwainforhisadvocacyofthiswork. however,showednosignificantdifferencesinthedietof We would also like to thank coastal sportfishermen maleandfemalecobiawithinarangeofcomparablesizes and the directors of coastal fishing tournaments in whichmaybeattributabletotherelativelylowsamplesize MississippiandFloridafortheirspiritofcooperation of males. Although not statistically different, we did in helping us obtain samples. We are grateful to encounterfishmorefrequentlyinthestomachsofmales RichardHeardandBruceComynsfortheirhelpinidentifying than females which also may be an indication of an the invertebrates and the fishes, respectively. The field ontogeneticshifttowardfishpreysincemostofthelarge assistance providedby Carol Cleveland, Mike Buchanan males, and not the large females, were includedin the andT.J.Beckerwasgreatlyappreciated.Wegiveourthanks male>femalecomparativeanalysis. toTerryMcBeeforhishelpinthefieldandforhisvaluable The species composition of the diet revealed that assistancewithdataanalysis. Ourgratitudeisextendedto cobiafedprimarilyonorneartheseafloor.Theportunids, BarbaraVLskupandDavidAbomforreviewinganearlier sicyoniids,penaeids,andstomatopods,thoughcapableof versionofthemanuscript.JefleryLotzalsoprovidedhelpful swimming,areprimarilybenthicorcpibenthicinhabitants. suggestions which improved the manuscript. The Octopi,as wellas many ofthe fishprey (e.g., bothids, constructivecommentsoftwoanonymousreviewerswere uranoscopids,airids,triglids,dasyatids,eels),alsoreside alsoappreciated. Wethankmarineenforcementpersonnel on or near the bottom. However, other prey such as oftheMississippiDept, ofWihllife,FisheriesandParksfor carangids,clupeids,andsquidarepelagicorganisms,and providinguswithsomespecimensofcobia.Fundingforthis their presence in the diet indicated flexibility in the studywasprovidedbytheU.S,Dept,oftheInterior,U.S. foragingbehaviorofcobia. Fish and Wildlife Service, Federal Aid in Sportfish Insummary,wefoundthattheprimaryfoodsofcobia RestorationProjectF-91, throughtheMississippi Dept,of from the northcentral Gulfof Mexico were benthic or MarineResources. 166 FoodofCobiafromNorthcentralGulfofMexico LiteratureCited Biesiot,P.M.,R.M.Caylor,andJ.S.Franks.1994.Biochemical Knapp, F.T. 1949. Menhaden utilizationinrelation to the and histological changes during ovarian developmentof conservationoffood and game fishes oftheTexasGulf cobia,Rachycentroncanadum,fromthenorthernGulfof Coast. TransAmFishSoc79:137-144. Mexico.FishBuU92:686*696. . 1951. Foodhabitsofthesergeantfrsh,/{ocAyc^nTro/i Boschung,H.T.,Jr. 1957. ThefishesofMobUeBayandtheGulf canadus. Copeia1951:101-102. coast of Alabama. Ph.D. Dissertation, Univ. Alabama, Migdalski,EC.,andG.S.Hchter.1983.Thefreshandsahwaterfishes Tuscaloosa,AL,626p. oflheworid. CrownPublisheis,Inc.,NewYcdc,pp.225-226. Briggs,J.C. 1958.AlistofFloridafrshesandtheirdistribution. Miles,D.W. 1949. Astudyofthefoodhabitsofthefishesofthe BullFlaStateMusBiolSci2:221-318. AransasBayarea. M.S.Thesis,Univ,Houston,TX,70p, Christmas,J.Y.,A.Perry,andR.S.Waller. 1974.Investigations Reid,G.K.,Jr. 1954, AnecologicalstudyoftheGulfofMexico ofcoastalpelagicfishes. CompRepBurCommFish fishes,inthevicinityofCedarKey,Florida. BullMarSci ProjNo.2-128-R. 105p. GulfCaribb4:1-94. Dawson,C.E. 1971. Occurrenceanddescriptionofprejuvenile Shaffer, R. V., and E. L. Nakamura. 1989. Synopsis of and earlyjuvenile GulfofMexico cobia, Rachycentron biological data on cobia Rachycentron canadurn canadurn, Copeia1971:65-71. (Pisces:Rachycentridae). NOAA Tech Rep, NMFS 82 Franks,J.S.,M.H.Zubear,andT.D.McIIwain.1991.Ttetidsinseasonal (FAOFishSynop153],21p. movementsofcobia, taggedandreleased Zar,J.H. 1984. Biostadsticalanalysis. 2nded. Prentice-Hall, inthenorthernGulfofMexico. JMissAcadSci36(1);55. Inc.,EnglewoodCliffs,N.J.,718p. 167

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