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C. Sah<strong>in</strong> et al. / Turk. J. Fish. Aquat. Sci. 6: 155-163 (2006) 15725Temperature (C) (ºC)201510508Mar. Apr. May Jun. Jul. Aug. Sep. Oct. Nov. Dec. Jan. Feb.DO (mg/L)DO (mgl -1 )7620519Mar. Apr. May Jun. Jul. Aug. Sep. Oct. Nov. Dec. Jan. Feb.Sal<strong>in</strong>ity (ppt)181716151,2Mar. Apr. May Jun. Jul. Aug. Sep. Oct. Nov. Dec. Jan. Feb.1Cholorphyll-aa0,80,60,40,20Mar. Apr. May Jun. Jul. Aug. Sep. Oct. Nov. Dec. Jan. Feb.Figure 2. Monthly variations <strong>in</strong> temperature, dissolved oxygen, sal<strong>in</strong>ity, <strong>and</strong> chlorophyll of the study area.1211<strong>Condition</strong> <strong>Index</strong> <strong>in</strong>dex10987654Mar Apr May Jun Jul Aug Sep Oct Nov Dec Jan FebK1K2Figure 3. Monthly variations <strong>in</strong> two condition <strong>in</strong>dexes.


160 C. Sah<strong>in</strong> et al. / Turk. J. Fish. Aquat. Sci. 6: 155-163 (2006)Table 2. <strong>Gonadal</strong> development phases of males <strong>and</strong> percentage distributionMonths Male Uncerta<strong>in</strong> I II III IV V VIN % N % N % N % N % N %March - 20 20 100 - - - - - - - - - -April - 20 20 100 - - - - - - - - - -May 25 - - - 16 64 6 24 3 12 - - - -June 24 - - - 3 13 7 28 10 42 4 17 - -July 27 - - - - - 3 11 8 30 18 67 - -August 28 - - - - - - - 4 14 13 46 11 40September 15 14 14 48 - - - - - - 6 21 9 31October 2 28 28 93 - - - - - - - 2 7November - 20 20 100 - - - - - - - - - -December - 20 20 100 - - - - - - - - - -January - 20 20 100 - - - - - - - - - -February - 20 20 100 - - - - - - - - - -100100a) Beg<strong>in</strong>n<strong>in</strong>g (primordial) Phase: Follicule walls are develop<strong>in</strong>g<strong>and</strong> oocyts are formed.b) Develop<strong>in</strong>g (immature) phase. Folliculs diameter <strong>in</strong>creased <strong>and</strong>oocytes are gett<strong>in</strong>g filled.4040c) Matur<strong>in</strong>g (mature) stage. Follicules are filled with completelymature oocyts.d) Spent (spawn) phase: Follicules are start<strong>in</strong>g to loose theirtypical structure.40e) Full spent phase: Follicules are gett<strong>in</strong>g smaller, connectivetissue re-formed <strong>and</strong> oocytes <strong>in</strong> some follicules absorbed40f) Rest<strong>in</strong>g phase: Gonad <strong>and</strong> <strong>in</strong>terfolliculer areas are fully coveredby connective tissue.Figure 6. Gonad development phases <strong>in</strong> females.


C. Sah<strong>in</strong> et al. / Turk. J. Fish. Aquat. Sci. 6: 155-163 (2006) 16110040a) Beg<strong>in</strong>n<strong>in</strong>g (primordial) phase: Follicle form<strong>in</strong>g stage <strong>in</strong> theconnect<strong>in</strong>g tissue <strong>and</strong> <strong>in</strong>tensive spermatozoid carry<strong>in</strong>g stage <strong>in</strong> thefollicles.b) Develop<strong>in</strong>g (immature) phase: Spermatozoid b<strong>and</strong>s are formed<strong>and</strong> connect<strong>in</strong>g tissue dim<strong>in</strong>ishes <strong>in</strong> this stage.4040c) Matur<strong>in</strong>g (mature) phase: nter follicles connect<strong>in</strong>g tissuedisappeared <strong>and</strong> follicles reach to maximum size.d) Spent (Spawn) phase: Follicle walls are gett<strong>in</strong>g th<strong>in</strong>ner, structuredeformities start <strong>and</strong> spermatozoid amount <strong>in</strong>creases10040e) Full spent phase: Complete destruction of the follicle walls <strong>and</strong>gonad volume fast covered by the connect<strong>in</strong>g tissuef) Rest<strong>in</strong>g phase: Gonad area is fully covered by the connect<strong>in</strong>gtissue.Figure 7. Gonad development phases <strong>in</strong> males.competition) variables. All the environmentalvariables may affect the growth <strong>and</strong> reproduction aswell as the distribution of Anadara <strong>in</strong>aequivalvis.Among the biotic variables the chlorophyll-a, an<strong>in</strong>dicator of phytoplankton biomass <strong>and</strong> a very wellknown source of food for bivalve molluscs, washighly correlated with condition <strong>in</strong>dex dur<strong>in</strong>g thepresent study. Highest levels of chlorophyll-a content<strong>and</strong> condition <strong>in</strong>dex matched very well dur<strong>in</strong>g April –May. It is known that good condition values are the<strong>in</strong>dicators of accumulat<strong>in</strong>g nutrient reserves,particularly glycogen <strong>and</strong> prote<strong>in</strong>, <strong>and</strong> gonadaldevelopment (Dare <strong>and</strong> Edwards, 1975; Bligh <strong>and</strong>Dyar, 1984; Aldrich <strong>and</strong> Crowley, 1986) . In presentstudy, two peaks <strong>in</strong> condition <strong>in</strong>dex were observeddur<strong>in</strong>g annual cycle (Figure 3); major one <strong>in</strong> May <strong>and</strong>second one <strong>in</strong> November. Gradually decreas<strong>in</strong>gcondition <strong>in</strong>dex from May to August <strong>in</strong>dicatedsignificant loses <strong>in</strong> tissue weight or reserves due torelease of gametes. After August condition <strong>in</strong>dexstarted to rise gradually reach<strong>in</strong>g second peak <strong>in</strong>November when autumn blooms occurs <strong>in</strong> the area.This is a typical seasonal cycle observed <strong>in</strong> bivalves<strong>in</strong> subtropical <strong>and</strong> temperate regions (Iglesias <strong>and</strong>


162 C. Sah<strong>in</strong> et al. / Turk. J. Fish. Aquat. Sci. 6: 155-163 (2006)Navarro, 1991).It is reported that there have been importantchanges <strong>in</strong> the metabolic activities <strong>in</strong> pre/postreproduction period of the bivalve molluscs (Okumu,1993; Moscose et al., 1992; Narasimham, 1988b).Significant decl<strong>in</strong>es <strong>in</strong> prote<strong>in</strong> <strong>and</strong> lipid levels are<strong>in</strong>evitable dur<strong>in</strong>g spawn<strong>in</strong>g season. In contrastreserves such as glycogen <strong>and</strong> lipid are utilized dur<strong>in</strong>gthe w<strong>in</strong>ter when available food is limited. <strong>Seasonal</strong>variation <strong>in</strong> condition <strong>in</strong>dex also reflects this fact(Figure 4) (Aldrich <strong>and</strong> Crowley, 1986; Devenport<strong>and</strong> Chen, 1987; Okumu, 1993). The results of thepresent study also exhibited similar pattern. The lipidcontent reached maximum levels dur<strong>in</strong>g autumn <strong>and</strong>was used as energy reserve dur<strong>in</strong>g w<strong>in</strong>ter. Dur<strong>in</strong>g thespr<strong>in</strong>g gonadal development caused slight <strong>in</strong>crement<strong>in</strong> prote<strong>in</strong> content but not <strong>in</strong> lipid. That is becauselipid was used as energy source for accelerat<strong>in</strong>gmetabolism due to <strong>in</strong>creas<strong>in</strong>g temperature <strong>and</strong>gametogenesis (Figure 4).Observation of histological samples of gonads<strong>in</strong>dicated that spawn<strong>in</strong>g <strong>in</strong> the Black Sea populationof A. <strong>in</strong>aequivalvis took place dur<strong>in</strong>g summer period.Native bivalve species <strong>in</strong> the Black Sea spawn earlierthan A. <strong>in</strong>aequivalvis. It is most likely that A.<strong>in</strong>aequivalvis as a tropical species needs highertemperatures for spawn<strong>in</strong>g <strong>and</strong> larval development.<strong>Gonadal</strong> development stages for other species ofAnadara (i.e., A. granosa <strong>and</strong> A. rehombea) fromvarious localities have been described as rest<strong>in</strong>g,beg<strong>in</strong>n<strong>in</strong>g, develop<strong>in</strong>g, matur<strong>in</strong>g <strong>and</strong> spent <strong>and</strong>differentiations between these phases seem to quitesimilar (Dzyuba, 1982). Studies on A. subcrenata, A.broughtoni <strong>and</strong> A. ursi <strong>in</strong> sub-tropics showed thatspawn<strong>in</strong>g took place from June to September(Morton, 1990; Moscose et al., 1992; Dzyuba <strong>and</strong>Maslennikova, 1982; Cruz, 1984; Yankson, 1982;Hadfield, <strong>and</strong> Anderson, 1988; Cruz, 1987; Trol <strong>and</strong>Gomez, 1985). Dur<strong>in</strong>g the present study females withmature gametes were found until September <strong>and</strong>October, but their ratios decl<strong>in</strong>ed rapidly after August(Table 1, Table 2).Sex ratios of the specimens sampled weredeterm<strong>in</strong>ed monthly from the histological slides(Figure 5) as 1.04:1 (F/M) <strong>and</strong> 2 has shown that thereis no significant difference between sex ratio. The sexratio for other Anadara populations is given <strong>in</strong> Table3. It can be clearly seen that there is good agreementwith f<strong>in</strong>d<strong>in</strong>g of present study (Table 3).Determ<strong>in</strong>ation of first maturity length <strong>and</strong>spawn<strong>in</strong>g period are the basic requirements for theprotection <strong>and</strong> susta<strong>in</strong>able exploitation of the stocks.There are several methods used for study<strong>in</strong>g thesevariables, however the most precise results haveobta<strong>in</strong>ed through histological exam<strong>in</strong>ations. It isalmost impossible to determ<strong>in</strong>e the beg<strong>in</strong>n<strong>in</strong>g (II)period of the gonadal development us<strong>in</strong>g otherapproaches. In conclusion, the <strong>in</strong>troduced bivalvespecies has been adapted <strong>in</strong>to new environmentexhibit<strong>in</strong>g similar seasonal cycles <strong>in</strong> condition <strong>in</strong>dex<strong>and</strong> gametogenesis with other species of the genusAnadara <strong>in</strong>habit<strong>in</strong>g sub-tropic <strong>and</strong> temperate waters<strong>and</strong> other bivalve species <strong>in</strong> the Black Sea.ReferencesAldrich, J.C. <strong>and</strong> Crowley, M. 1986. <strong>Condition</strong> <strong>and</strong>Variability <strong>in</strong> Mytilus edulis (L.) From DifferentHabitats <strong>in</strong> Irel<strong>and</strong>, Aquaculture, 52: 273-286.Alpbaz, G.A. <strong>and</strong> Önen, M. 1991. Türkiye’de hraç EdilenKum Midyesi (Venus gall<strong>in</strong>a) Üzer<strong>in</strong>e Aratırma,E.Ü. Su Ürünleri Dergisi, 7: 78-86.AOAC. 1990. Official Methods of Analysis. In: K. Heldrich(Ed.), Association of Analytical Chemists. 15 thedition. AOAC: Arl<strong>in</strong>gton, Virg<strong>in</strong>ia, USA, 1289 pp.Bligh, E.G. <strong>and</strong> Dyar, W.J. 1984. Rapid Method of TotalLipid Extraction <strong>and</strong> purification, Canadian Journal ofBiochemistry Physiology, 37: 911-917.Broom, M.J. 1985. The Biology <strong>and</strong> Culture of Mar<strong>in</strong>eBivalve Molluscs of the Genus Anadara, ICLARMStudies <strong>and</strong> Rewiews, 209: 1-37.Cruz, R.A. 1984. Some Aspect of the Reproduction ofAnadara tuberculosa (Plecypoda: Arcidae) FromPunta Morales, Punterenas, Costa Rica, Rev. Biol.Trop., 32: 45-50.Cruz, R.A. 1987. The reproductive Cycle of the MangroveCockle Anadara gr<strong>and</strong>is (Bivalvia: Arcidae) <strong>in</strong> CostaRica, Brenesia, 27: 1-8.Dare, PJ. <strong>and</strong> Edwards, D.B. 1975. <strong>Seasonal</strong> Changes <strong>in</strong>Flesh <strong>and</strong> Weight <strong>and</strong> Biochemical Composition ofMussels (Mytilus edulis L.) <strong>in</strong> the Conwy Estuary,North Wales, J. Exp. Mar. Biol. Ecol., 18: 89-97Devenport, J. <strong>and</strong> Chen, X. 1987. A Comparison ofMethods For the Assessment of <strong>Condition</strong> <strong>in</strong> theMussel (Mytilus edulis L.), J. Moll. Stud., 53: 293-297.Dzyuba, S.M. <strong>and</strong> Maslennikova, L.A. 1982. Reproductivecycle of the Bivalve Mollusc Anadara broughtoniFrom the Southern Peter the Great Bay of the SeaJapan, Biol Morya., 3: 34-40.Table 3. Sex ratios <strong>in</strong> some Anadara speciesCountry Species Sex Ratio (F/M) ResearchersIndia A. granosa 1:1 Narasimham, 1988Costa Rica A. tuberculosa 1:1 Cruz, 1984Philipp<strong>in</strong>es A. antiquata 1.03:1 Toral, 1985East Africa A. senilis 1.2:1 Yankson, 1982Australia A. trabezia 1:1 Hadfield, 1988Costa Rica A. gr<strong>and</strong>is 1.2:1 Cruz, 1987Turkey A. <strong>in</strong>aequivalvis 1.04:1 This research


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