International Journal of Animal and Veterinary Advances 1(2): 66-72, 2009 ISSN: 2041-2908 © M axwell Scientific Organization, 2009 Submitted Date: August 17, 2009 Accepted Date: September 24, 2009 Published Date: October 30, 2009 A Study of the Length -Weight Relationship and Condition Factor of Callinectes amicola (De Rochebrune, 1883) from Okpoka Creek, Niger Delta, Nigeria 1 1 J.F.N. Abowei and 2 A.D.I. George Department of Biological Sciences, Faculty of Science, Niger Delta University, Wilberforce Island, Amassoma, Bayelsa State, Nigeria. 2 Departm ent of Fisheries and A quatic Environment, Faculty of Agriculture, Riv ers State University of Science and Technology, Port Harcourt, Rivers State, Nigeria. Abstract: The length - weight relationship and condition factor of Callinectes amicola from O kpoka C reek in the Niger Delta area of Nigeria was studied for a period of one year. The exponent ‘b’ values for all the sexes ranged from 2.336 and 2.56 (males), 2.367 and 2.536 (females) and 2.352 and 2.548 (combined sexes) respectively. Growth generally exhibited a negative allometry in all the sexes as shown by the mean exp onents (b=2.448) for male, female (b=2.451), combined sex (b=2.449). Generally, the regression equations revealed high correlation in all the sexes as the correlation coefficient (r) values for male (0.951), female (0.971) and combined sexes (0.961) are very close to r = 1. The monthly K values of the males ranged from 0.0984 and 0.1503 (mean = 0.1214). The estimated K value for both sexes combined was 0.1260. Similarly, estimated K values for the females ranged from 0.0889 – 0.1524.The overall mean K value for the females was 0.1229. The minimum K value (0.098 4) for the male was observed in February. The female C. am nicola minimum K value (0.0889) an d Kmax (0.158 0) valu es w ere ob tained in No vem ber. Key w ords: Callinectes amicola, length -weight relationship, cond ition facto r, Okpoka Cre ek an d Nigeria INTRODUCTION The blue crab Callinectes amnicola belongs to the family Poruntidae. It is famous and one of the most important economic swimming crabs present in the brackish wetland and lag oons in Nigeria (Abbey-Kalio, 1982; Solarin, 1988). These crabs inhabit muddy bottoms in mangrove areas and River mouths (Defelice et al., 2001). This crustacean in the most important food organism caught in the coastal (inshore) fishery and lagoons in west Africa (Lawal-Are et al., 2000). The species is generally cherished source of protein and minerals in human diet and animal feeds (Chindah et al., 2000; Em man uel (20 08). These crabs are gonochoristic and physiological maturity in males in reached when the carapace attains a length of between 90 and 110 mm . The male and female usua lly begins their mating process wh en a female is in a premolting condition. The crabs remain paired for 3 to 4 days until the female molts and the n they copu late (Knuckey, 1996). The fem ale then migrates offshore with the fertilized eggs, where they hatch in a couple of weeks. They can deliver an extremely painful pinch and are noted for being particularly aggressive and difficult to handle safely. Even when out of the water, they will lunge towards m ovemen t they consider a threat. Blue crabs are blue because their she ll contains a number of pigments, including Alpha-crustacyanin, which interacts with a red pigment, astaxanthin, to form a greenish-blue coloration. When the crab is cooked, the Alpha-cru stacyanin breaks down, leaving only the astaxanthin, which turns the crab red-orange. Length-weight relationship (LW R) and its parameters ‘a’ and ‘b’ are of great impo rtance in fishery biology and practical assessment of stocks of aquatic species (Gulland, 1983; Enin, 199 4; Stergiou and M outopou los, 2001). Pauly (1993) suggested the following situations when length-weight relationship may be needed . C C C C The conv ersion of length of individual fish to we ight. Estimating the mean weight of fish of a given length. Conversion of growth equation for length into a growth equation for weight, and Morphological comparisons between populations of the sam e species or b etween species. L W R can also be useful in studies of gonad de velop men t, rate of feeding, metamorphosis, maturity and well being of the fish p opulation (L e Cre n, 1951; Bolger and Connolly, 1989). Length-weight relationship data may be incorporated into a database such as fish base (Froese, 1990; Pauly and Froese, 1991) for easy access, retrieval and use for any assessmen t work. The growth exponent ‘b’ in the LWR has values between 2 and 5 (Bagenal and Tesch, 1978). They observed that when the expon ent ‘b’ is 3, it indicates Corresponding Author: J.F.N. Abowei, Department of Biological Sciences, Faculty of Science, Niger Delta University, Wilberforce Island, Amassoma, Bayelsa State, Nigeria. 66 Int. J. Anim. Veter. Adv., 1(2): 66-72, 2009 area of 206Km 2 and extends 7Km offshore to a depth of about 7.5 metres (Irving, 19 62, Scott, 1966 and Alalibo, 1988). The Bonny River is a major shipping route for crude oil and other cargoes, and leads to the Port Harco urt quays, Federal Ocean Terminal, Onne, and Port Harcourt Refinery company terminal jetty, Okirika. Specifically, the Okpoka creek lies between Longitudes 7 ° 03! and 7 ° 05! East and Latitudes 4° 06! and 4°24! and it is about 6 kilom eters lon g. Characteristically, the area is a typical estuarine tidal water zone with little fresh water input but with extensive mangrove swamps, inter-tidal mud flats, and influenced by semi-diurnal tidal regime. In the Bonny River estuary, the salinity fluctuates with the sea son and tide regime is influenced by the Atlan tic ocean (D angana, 1985). Tidal range in the area is about 0.8m at neap tides and 2.20m during spring tides (N ED EC O, 1961). It is strategically located southwestern flanks of Port Harco urt and O kirika of Rive rs State. The creek is bounded by thick mangrove forest dominated by Rhizophora species interspersed by White mangrove (Avecinia sp.) and Nypa palm. Along the shores of the creek are located the Port Harcourt Trans- Amadi Industrial layout, several establishments, markets, the main Port Harcourt Zoological garden and several commu nities. The communities are Oginigba, Woji New layout, Azuabie, Okujagu- Ama, Ojimba- Ama, Abuloma, Okuru- Ama, Oba-Ama and Kalio- Ama. Artisanal fishers mainly exploit the fisheries. The fishers use wooden/dug-out canoes ranging in size from 3 to 8m long. T he canoes are either pad dled or powered by small outboard engines, and manned by an average of two men. From these boats, the fishers operate their cast nets, hook and lines, gillnets, crab pots, etc. isometric growth (without changing body shape) but when below or abo ve 3, growth is allometric (i.e., fish changes shape as it grows larger). How ever, Pauly (1993) while lam enting on the lack of adeq uate theory to guide research w ork an d form ulate testable hypothesis on the LWR of fish and aq uatic invertebrates, stated that “there is no theory tha t tells us in which case estimated b value can be expe cted to be below 3 (negative allom etry) or above 3 (positive allometry). The condition factor is an estimation of the general well being of fish and crustaceans (Oni et al., 1985; Jones et al., 1999). It is based on the hypothe sis that heavier individuals of a given length are in better condition than less weightier ones (Bagenal and Tesch, 1978). Condition factor has been used as an index of growth and feeding intensity. W eatherly and Rogers (1978) posited that condition factor of different populations of same species is indicative of food supply and timing and duration of breed ing. Consequently, several studies have been carried out in this regard for finfish species and crustaceans. Notable among these are the reports of Stickney, (1972) on fishes and invertebrates in Georgia Coastal water, Georgia. Olm i and Bishop , (1983) on the blue crab Callinectes sapidus Rathbun from the Ashley River, South Carolina; Prasad, et al., (1989 ) on three Portunid crab species; Enin, (1994) on two W est African prawns (Nematopalaemon hastatus and Macrobrach ium macrobrachion) from the C ross River estuary, Nigeria; Enin, et al., (1996) on estuarine prawn Nematopalaemon hastatus off the South East coast of Nigeria; Sukumaran and Neelakantan (1997) on two marine Portunid crabs (Portunus sanguinolentus and Portunus pelagicus) from the Kamalaka coast, India. Villasm il et al., (1997) on the blue crab Callinectes sapidus in Lake M aracalbo, C lencia (Ma racalbo); Tabash (2001) on the blue crab Callinectes arcuatus in the Gulf of Nicoya, Costa Rica; Atar and Secer (2003) on the blue crab (Callinectes sapidus in Beymelek Lagoon lake, Antalya, Turkey and Yakub and Ansa (2007) on the pink Shrimp Penaeus notialis and Giant tiger shrim p, Penaeus monodon of Buguma creek in the N iger D elta, Nigeria. There is a dearth of information on length-weight relationships on the swimming crabs (Genus Callinectes) from Nigerian waters pa rticularly fro m the Niger Delta estuarine waters for the evaluation of its ecology with a view to effectively m anag e the resourc es for su stainable supply to the citizenry. Sampling stations: Six samp ling stations were established along a spatial grid of the Okpoka creek covering a distan ce of about six kilometers. The sampling stations were established based on ecological settings, vegetation and h uma n activities in the area. The sampling station is about one kilometer apart from each other. Station 1: Located upstream of the Po rt Harc ourt m ain abattoir at Oginigba waterfront with living houses on the left flank of the shoreline. Vegeta tion is sparse w ith mainly red mangrove (Rhizophora sp.,) white mangrove, Avicenia sp. and Nypa palm (Nypa fructicans). Station 2: Situated at Az uabie / Port H arcourt m ain abattoir waterfront. It is located downstream of Station 1. The bank fringing the Azuabie/abattoir is bare with no visible plants except toilet houses, residential houses, animal pens, boats and badges, while at the opposite side there are few mangrove and Nypa palm. Human activities here include slaughtering of animals, marketing, fishing and boat building. It is located downstream of station 1 and it is main collection point of abattoir wastes and other human and market wastes. MATERIALS AND METHODS Study Area: The study was carried out in Okpoka creek, which is one of the several adjoining creeks off the Upper Bonny Rive r estuary in the Niger Delta (Fig. 1). The Bonny River Estuary lies on the Southeastern edge of the Niger Delta, between longitudes 6°58! and 7°14!! East, and latitudes 4°19!! and 4°34! North. It has an estimated 67 Int. J. Anim. Veter. Adv., 1(2): 66-72, 2009 Fig. 1: Map of Niger Delta showing Rivers State and the Study Area. Station 3: It is dow nstream from the Port Ha rcourt abattoir at the Woji sand-Crete. It is about one kilometer away from Station 2. The major activities here included sand mining and loading. Station 5: Is situated at Ojimba cum Abuloma waterfronts. There are no commercial activities apart from ferryboats operations. The shoreline fringes have mainly Nypa palm. The area is shallow and at low tide, the greater part of the bottom mud flat is exposed. Station 4: This station is located at Okujagu-Ama area. There are no industrial activities here. Mainly fishers occupy the area. Nypa palm dominates the marginal vegetation while the op posite side is thickly populated with red mangrove forest. Rhizophora racem osa and Rhizophora mangle. The main activity is fishing, boat ferrying and occasional sand moving. Station 6: Is located in front of Kalio-ama directly between Okpoka and Amadi creeks. The human activities here include jetty operations, oil and non-oil industrial activities, boat traffic and fishing. Vegetation is few dominated by red man grove interspersed with wh ite mangrove Avicenia africana. 68 Int. J. Anim. Veter. Adv., 1(2): 66-72, 2009 Table 1: Least squ are reg ressio n eq uatio n, ex pon ent (b ), interce pt (a), c orrela tion c oeff icien t (r) and rang es o f Ca llinecte s am nico la Sex Regression r b Equation M ale W = - 2.356L 2 . 4 4 8 (0.935-0.963) 0.951 (2.336-2.561) 2.448 Fem ale W = - 2.392L 2 . 4 5 1 (0.962-0.978) 0.971 (2.367-2.536) 2.451 Comb ined sex W = - 2.373L 2 . 4 4 9 (0.948-0.970) 0.961 (2.352-2.548) 2.449 () = Range values the Length-W eigh t relatio nsh ip in a (-2.156 to -2.688) -2.356 (-2.215 to – 2.496) -2.392 (-2.215 to -2.592) -2.373 millimeter (mm) while weight measurement was done using a 0.001g precision Adam (PGW series) weighing balance to the nearest gram s (g). The length-weight relationships of all samples collected were determined for the various sexes by the expression: W = aL b (Le Cren, 1951; Pauly, 1983) (1) W here: W = the derived weight (a) L = th e carapace length (mm ) or width a = the intercept of the regression curve b = the regression coefficient (slope) The parameters ‘a’ (intercept) and ‘b’ (slope) are easily estimated by the linear regression based on Logarithms as Plate 1: Crab traps and other fishing materials LogW = Log a + blogL (Lagler, 1968) Sample collection: The crabs for study were collected fortnigh tly for twe lve (12 ) calendar m onths (January to Decembe r, 2007) using the square lift ne t trap (Plate 1) at each of the sa mpling stations along the Okpoka creek. The lift net trap has a sq uare structure made of wooden stick of about 4cm thick and an area of 4.9m 2 . The mesh sizes of the bag-like net were 1.2cm to 2.0cm multifilament nylon. The length of the bag is 40 to 60 cm. Strong nylon cords were woven in a net-like fashion from the centre to the middle of each of the four edges. A twine of about 6m long w as attached to the centre and the other free end of the twine was tied to a floater, which served as a marker on the water surface to show the position of the gear. The lift net trap was baited at the centre with animal offal and fish. The trap was operated from a hand-paddled canoe manned by two persons; one rowing while the other sets and hulls the trap into and from the water. The crabs were caught trapped and most of them were observed feasting on the bait until they were hulled into the boat. Sampling lasted for 4 hours on every sampling day and samples were collected between low ebbing and low flooding tide periods. The catches were taken to the laboratory in a cooler and stored in a deep freezer for further analysis. Crabs were identified to species level carried out using photo cards and availab le identification keys (Fischer, 1978; Williams, 1974; Schneider, 1990). Therefore each crab was sorted into species, sex and the required metric measurements were taken. The carapace w idth and length w ere measured w ith a 0.5mm precision vernier caliper to the nearest (2) The pattern of grow th (isom etric or allometric) in C.amnicola was determined from the value of ‘b’ in the equation W = aL b . The linear regression routine option 3 in FiSAT (FAO – ICLA RM Stock Assessm ent Tool) software (Gayanilo et al., 1995) using Plll 950 MHZ computer for the analysis. In the analysis, only the midLengths and mean weights of the classes are required by FiSA T (Gayanilo and Pauly, 199 7). The Fulton’s condition factor (K) was estimated from mean length and mean weight in the sample using the relationship K = 100 W (Gayanilo et al.,1997) L3 W here: K = Condition factor W = mean weight of crab (g) L = mean length of crab (mm) (3) RESULTS The results of length-weight relationship (L W R) study using the log-log transformation an d linear square regression analysis meth od are presented in Table 1. The exponent ‘b’ values for all the sexes ranged from 2.336 and 2.56 (males), 2.367 and 2.536 (females) and 2.352 and 2.548 (combined sexes) respectively (Table 1). The grow th gen erally exhibited a negative allometry in all the sexes as shown by the mean exponents (b = 2.448) for male, female (b = 2.451), combined sex (b = 2.449). The scatter diagrams for the length weight relationship for 69 Int. J. Anim. Veter. Adv., 1(2): 66-72, 2009 Table 2: M onth ly Condition factor for male C alline ctes a mn icola in Okpoka C reek M onth Co ndition f actor Jan. 0.1115 Feb. 0.984 March 0.1247 Ap ril 0.1294 May 0.1453 June 0.1503 July 0.1236 Aug. 0.108 Sep t. 0.1214 Oc t. 0.1238 Nov. 0.1055 Dec. 0.1144 Tab le 3: Mon thly Condition factor for female Ca llinecte s am nico la in Okpoka Creek. M onth Condition factor Jan. 0.0966 Feb. 0.1099 March 0.1289 Ap ril 0.1524 May 0.1041 June 0.1416 July 0.1256 Aug. 0.0989 Sep t. 0.1351 Oc t. 0.1339 Nov. 0.0889 Dec. 0.1006 Fig. 3: Length-Weight relationship of female C. amnicola Fig. 4: Length-Weight relationship of Combined sexes of C. amnicola the minimum K value (0.0889) and Kmax (0.1580) values were obtained in Novem ber. DISCUSSION The observed values of the regression coefficient (b) for the males, females and combined sexes (male = 2.448, Fem ale = 2.451 and com bined sexes = 2.499) less than 3 are indication of negative allom etric growth. This is in agreement with the results from Badagry, Lagos and Lekki lagoons for the same species by (Law al-Are, 2003). The b values obtained in this study also agreed with values obtained for C. sapidus from G eorgia (Stickney, 1972) and Beymelek Lagoon Lake, Turkey (Atar and Secer, 2003). How ever, these results are contrary to what was observed in Lag os lagoon and it ad jacent creeks on the same species by Emmanuel, (2008), who reported a positive allometric grow th for C. amnicola. Akin-Oriola et al (2005) also reported b>3 (positive allometric growth) for Callinectes pallidus from Ojo Creek in Badagry, Lagos state. Generally, the regression lines revealed a high correlation in all the sexes since the correlation coefficient (r) values are very close to unity. This observation is indicative of a very positive correlation between carapace length and total weight in this species. This agree d with Fig. 2: Length-Weight relationship of male C. amnicola male, female and combined sexes are illustrated in Fig. 2, 3 and 4 respectively. Generally, the regression equations revealed high correlation in all the sexes as the correlation coefficient (r) values for male (0.951 ), female (0.971) and combined sexes (0.961) are very close to r = 1. The results of the monthly mean condition factor (K) for the males an d fem ales, C. am nicola are shown in Tables 2 and 3 respectively. The monthly K values of the males ranged from 0.0984 and 0.150 3 (mean = 0.12 14). The estimated K value for both sexes combined was 0.1260. Similarly, estimated K v alues for the females ranged from 0.0889 – 0.1524. The overall mean K value for the females was 0.1229. The minimum K value (0.0984) for the male was observed in February In respect of the female C. am nicola 70 Int. J. Anim. Veter. Adv., 1(2): 66-72, 2009 the report on the same species from Badagry, Lagos and Lekki Lagoons by (Lawal-Are, 2003) and the results on the species from Lagos lagoon and adjacent creeks by Emmanuel (2008). Similar trend was also observed on two Macrobrachium macrobrachium by (Enin, 19 94) in the Cross River estuary of Niger Delta. The results of the condition factor were neither sex nor season dependent. There was no significant variations (#0.05) between sexes. The similarity of the condition factors in the male and female crabs may be attributed probably to the absence of ov igerou s females. Branco and Masunari (2000) reported difference in condition factor of male and female Callinectes danae from Conceicao Lagoon sy stem, Santa Catarina, Brazil. They observed that it was probably due to higher weight of the female gonads of the crabs. However, in contrast to this result, Lawa l-Are and Kuse miju (2000 ) and Emmanuel (2008) observed differences in the co ndition factor of the different sexes of Callinectes amnicola in Badagry Lagoon and Lagos Lagoon and its adjacent creek . Law al-Are and K usem iju, (2000) reported higher condition factor in male than females crab s in Bada gry Lagoon Nigeria. Also while Emmanuel, (2008) observed in his study at Lagos Lagoon and its adjacent creek higher condition factor in the males than the female crabs. H e also observed that condition factor was lower in the smaller crabs. In fact, Warner (1977) reported that in true crabs, the males showed a higher condition factor than the females. This supports the slightly higher mea n K value (0.1260) of the male than that of the female (K = 0.1229) observed in this study. The non-seasonality, non significant variations between sexes may be related to food regime of the crab species utilizing food resources and accumulating a large quantity of flesh as was also observed by Ikomi and Sikoki, (2001) for fish in their study. Bagenal, T.B. and F .W . Tesch, 1978. Age and Growth. In: Method s for A ssessing of F ish Pro duction in Freshwaters. Bagenal, T.B. (Ed.). 3rd Edn. No. 3, Blackwell Scientific Publication Ltd., pp: 101-136. Bolger, J. and P.I. Connolly, 1989. The selection of suitable indices for measurement and analysis of fisheries cond ition. J. Fish Biol., 34(2): 17 1-182. Branco, J.O. and S. Masunari, 2000. Reproductive ecology of the blue crab, Callinectes danae, Smith, 1869 in the conceicao Lagoon system, Santa Catarina Isle, Brazil. Rev. Brasil. Zool., 17(3): 51-70. Chindah, A.C., C.C.B. Tawari and K.A. Ifechukwude, 2000. The food and feeding habits of the swimming crab, Callinectes amnicola (Portunidae) of the New Calabar River, Nigeria. J. 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