Revista de Biologia e Ciências da Terra ISSN: 1519-5228 [email protected] Universidade Estadual da Paraíba Brasil Araújo Montenegro, Ana Karla; Crispim, Maria Cristina; Torelli, Jane; Araújo Marinho, Randolpho Sávio The influence of the methodology in the results of food diet analysis of Steindachnerina notonota (MIRANDA RIBEIRO, 1937), in Taperoá II Dam, Paraiba State Revista de Biologia e Ciências da Terra, vol. Supl., núm. 1, 2006, pp. 180-191 Universidade Estadual da Paraíba Paraíba, Brasil Disponível em: http://www.redalyc.org/articulo.oa?id=50009917 Como citar este artigo Número completo Mais artigos Home da revista no Redalyc Sistema de Informação Científica Rede de Revistas Científicas da América Latina, Caribe , Espanha e Portugal Projeto acadêmico sem fins lucrativos desenvolvido no âmbito da iniciativa Acesso Aberto REVISTA DE BIOLOGIA E CIÊNCIAS DA TERRA ISSN 1519-5228 Suplemento Especial - Número 1 - 2º Semestre 2006 The influence of the methodology in the results of food diet analysis of Steindachnerina notonota (MIRANDA RIBEIRO, 1937), in Taperoá II Dam, Paraiba State Ana Karla Araújo Montenegro1; Maria Cristina Crispim2; Jane Torelli3; Randolpho Sávio Araújo Marinho4 ABSTRACT Several studies related with fish food diet, showed different methods of fish gut contents analysis.. Nevertheless, few works have been proposed to compare the fixation methods to preserve the feeding contents in fish gut. This work aimed to verify the influence of the methodology in the food diet analysis of Steindachnerina notonota (Miranda Ribeiro, 1937), in Taperoá II Dam in paraiban semiarid. The fishes used in this study had similar size. This region exhibit the lowest precipitation values of Brazil, with two seasonal periods the rainy and dry one, the later lasting longer than 8 months. The sampling was realized in March 2006, during day and night periods, using hand nets, trap nets and drag nets. In the field part of the sampling was preserved in 10% formalin and the other part in ice. In the laboratory the ice sample was preserved in formalin also. Test t (p<0.05) was applied to verify if there were siginifficant differences between the tested methodologies. Food diet based in both methodologies registered 71 food items, being 53.6% common to both samples, 83.1% were exclusive from formalin samples and 69.0% were exclusive from the ice samples, However the opposite items of the formalin food components that were abundant in these samples were scarce. The mean frequence of food items by stomach in the formalin sample was superior comparing with the ice sample 22.1±6.7 and 13.6±5.3, respectively, presenting significant differences among food diet analyzed (t = 3.82; p<0.01). The feed items from the ice sample showed a bad preservation, making the identification difficult. We can conclude that the species showed a food diet based in detritus, associated with vegetable remains and microalgae, independent of the methodology used. The formalin sample presented a better methodology, with more diverse food items and a better preservation making the identification of the contents in the gut easier, so we recommend this kind of method for diet content analysis in fish guts. Keyords: methodology, food diet, Steindachnerina notonota, Caatinga aquatic environments RESUMO Vários estudos relacionados com a dieta alimentar de peixes, têm apresentado diversos métodos de análises do conteúdo, revisão de técnicas que têm sido mais empregadas, dentre outros. Entretanto, poucos trabalhos têm sido propostos com a finalidade de comparar as formas de fixação do conteúdo estomacal. Este trabalho tem por objetivo, verificar a influência da metodologia na análise da dieta alimentar de Steindachnerina notonota (Miranda Ribeiro, 1937), do açude Taperoá II no semi-árido paraibano. A região apresenta os menores índices pluviométricos do Brasil com duas estações climáticas bem definidas, a chuvosa e a de estiagem que é superior a 8 meses. A coleta foi realizada no mês de março de 2006, nos períodos diurno e noturno, fazendo uso de tarrafas, redes de espera e 180 arrasto. Uma parte da amostra coletada foi fixada com formalina a 10% no próprio local da coleta e a outra acondicionada numa caixa térmica com gelo e posteriormente fixada no laboratório. Aplicou-se o teste t (p < 0,05), para verificar se houve diferença significativa entre as duas metodologias. A dieta alimentar de S. notonota, com base nas duas metodologias empregadas, registrou um total de 71 itens alimentares, sendo que 53,6% destes são comuns as duas, sendo 83,1% registrados para a amostra formolizada no campo e 69,0% para a previamente congelada. A freqüência média dos itens alimentares por estômago na amostra formolizada diretamente no campo foi superior à previamente congelada, 22,1±6,7 e 13,6±5,3, respectivamente, apresentando diferenças significativas entre as dietas (t = 3,82; p<0,01). Os itens alimentares provenientes da amostra previamente congelada apresentaramse mal conservados e das muitas vezes de difícil identificação. Concluiu-se que, a espécie apresentou uma dieta à base de detritos associada principalmente, a restos vegetais e microalgas, independente da metodologia empregada. A dieta alimentar da amostra previamente formolizada apresentou uma variedade de itens superior à congelada, sendo portanto, a mais indicada para uma determinação precisa. Palavras-chave: metodologia, dieta alimentar, Steindachnerina notonota, ambientes aquáticos da Caatinga 1 INTRODUÇÃO The trophic ecology of fishes give us great information about the relationships among fishes, the rest of aquatic organisms and quality of the water body, acknowledging the need to support for the management of conservation programs to improve the environment. Nevertheless, the majority of studies about fish trophic ecology in Brazil are only with commercial interesting species and some studies about the environment impact caused by hidrelectrical constructions (FERREIRA, 2004). Although a great number of fish species are not of commercial importance, research about the feeding of this group are important to provide information about fish stocks because they can be protential competitors or predators of commercial species, interfering in their death rates (HOFLING et al. 2000). Following Rodrigues (1987), in the northeast region of Brazil, studies about feeding have been developed in order to give support to the commercial exploration, estuarine and marine cultivation and reintroduction in reservoirs. This region shows the more changed aquatic environments in the country, especially due to the deforestation and the introduction of exotic species in dams by the Departamento Nacional de Obras Contra as Secas (DNOCS) (GURGEL, 1998; GURGEL et al., 2002). Several studies related with the trophic ecology of fishes have presented different methods to analyse the food diet, (HYNES, 1950; HELLAWELL & ABEL, 1971; KAWAKAMI & VAZZOLER, 1980), revisons of the more frequent methodologies (HAHN & DELARIVA, 2003), as well the elaboration of new methods for this kind of study (ARANHA, 1993). Some studies show the advantage or disadvantage of the different methods of fixation of gut contents, Prejs (1981) e Zavala-Camin (1996), but none compared the efficacy of different preservation methods in the same study. Among the studies related with food diet, some used formalin as a mean of conservation of gut contents, in the local of fishing, Santos (1981; 1982), Perrone & Vieira (1991), Vitule (2002), Giora & Fialho (2003), Kone (2003), Hermes-Silva et al. (2004), Alvim & Peret (2004), Ferreira (2004), Melo et al. (2004), Mérona & Rankin-De-Merona (2004), Moraes et al. (2004), Novakowski et al. (2004), Pelicice & Agostinho (2005), while 181 others used the freezing and later in laboratory used the formalin, Soares et al. (1998), Hofling et al. (2000), Dias et al. (2001), Gurgel et al. (2002), Cardoso et al. (2003), Chaves et al. (2003); Hajisamae et al. (2003), Mazzoni & Resende (2003), Torelli et al. (2003), Cardoso et al. (2004a; 2004b), Chaves (2004), Marinho et al. (2004a; 2004b), Teixeira & Gurgel (2004), Torelli (2004), Araújo et al. (2005), Montenegro et al. (2005). Nevertherless few studies have been focused in the comparison of the different gut content fixation methods. It is important to know which is the best way, because the results of a study about feeding habits depends on the accuracy to observe the different items, and the fixation of them. When not well preserved, the food items can not be identified, because they suffer a decomposition process, specially the animal ones, they decompose faster then vegetal or algal ones, because they present a cellular wall that delayed the digestion process. The aim of this work is to verify the influence of the preservation methodology on the food items analysis in Steindachnerina notonota (Miranda Ribeiro, 1937) gut contents, in the Taperoá II dam in Caatinga region of Paraíba state. 2 METHODOLOGY This work was developed with material from Taperoá II dam which is located in central region of Paraíba state (Fig. 1) between 07°11’44”S e 07°13’44”S and 36°52’03” W e 36°50’09” W coordinates is part of Taperoá River Basin, being used for human and animal water supply (PARAÍBA, 2000). The region show the lower pluviometric indices of Brazil (DANTAS, 2003), between 350 e 600 mm/year, besides high evaporation indices with two well defined seasons the rainy from 3 a 4 months and the dry one the rest of the year (BARBOSA, 2002). Fig. 1 – Map showing colecting places (from 1 to 4) in Taperoá II dam, paraiban semi-arid. Source: (BARBOSA, 2002). The study species Steindachnerina notonota, usually known as “sagüiru”, belongs to Curimatidae Family, is constituted by small indivuduals, completely lack of iliophag teeth, feeding on the bottom detrits of the environments (BRITSKI, 1970). Its endemic of the ecoregion of Maranhão-Piauí and Middle Northeast and has their phylogenetic relations not well defined (ROSA et al., 2005). These organisms migrate for reproduction. This species was selected specifically for its high capture frequence, and its importance in the food net among grazing species. Although it is not important commercially, it is used by population as a protein source. Nevertheless there are few studies about the eed habits of this species. Sampling took place in March 2006, during day and night periods, using hand nets of 15 mm, drag nets de 0,2 mm of mesh and with 10 meters of length, hand nets of 0,2 mm 182 and trap nets of 15, 20 e 25 mm, among together knots. In the field the separation, identification and biometry of specimens was developed. 10 animals were fixed in a 10% formalin, injected by a syringe in order to optimize the preservation, another 10 were kept cold in ice and transported in thermos boxes to the laboratory of Aquatic Ecology/DSE/UFPB, where they were kept frozen and only 24 or 48 hours the guts were preserved in formalin. We had the care of work with animals similar in length, in order not to allow differences dependent of the age. Afterwards, the guts of both groups of animals were taken off and transfered to a 70% alcohol flasks, where they remained untill be analyzed. The taxonomic identification of the fishes was based in Vari (1991). Some individuals were separated and sent to the Ictiological Collection of UFPB. For the knowledge of the food diet, the gut contents were analyzed in the individuals from both samples (formalized and frosty). The gut contents were analyzed macro and microscopically. The diet items were classified to lowest taxonomic category possible. For the determination of diet habits the frequency of occurrence method was applied (ZAVALACAMIM, 1996). T test was used (p < 0,05), to verify if there was significantly differences among the frequency mean of food item between the both methodologies. 3 RESULTS AND DISCUSSION The specimens analyzed presented maximum length of 10.7 cm and minimum of 7.2 cm, with a mean of 9.2 cm, and maximum weight of 33.6 g and minimum of 11.2, with mean of 23.0 g. The results of the food diet of S. notonota, based in both methodologies registered 71 food item being 50.70 % common to both samples, 83.09% observed in formalized sample and 69.01 in the frosty sample (Table I). Table I - Frequency of occurrence of item present in the food diet of S. notonota, applying both methodologies. Food Item Formolizada X Congelada X Superior vegetable remains X X Seeds X X Eggs X X Detritus Microalgae Bacyllariophyceae Acnanthes sp X Caloneis bacillum (Grunow) Cleve (1894) X X Cocconeis sp Cyclotella meneghiniana F.T. Kützing(1844) X Cymbella sp X X Diploneis sp X Ephitemia sp X Eunotia sp X Fragilaria sp X X Gomphoneis sp X X Gyrosigma sp X X Mastogloia smithii Thwaites ex W. Smith 1856 X X Melosira granulata (Ehrenberg) Ralfs in Pritchard 1861 X X Navícula sp X X Neidium sp X 183 Nitzschia sp X Pinnularia sp X X X X Rhopalodia sp Surirella sp X X Synedra ulna (Nitzsch) Ehrenberg 1832 X X Alga filamentosa X X Ankistrodesmus falcatus (Corda) Ralfs 1848 X X Ankistrodesmus spiralis (W.B. Turner) Lemmermann 1908 X X Chlorella vulgaris Beijerinck 1890 X X Closterium sp X Chlorophyceae Cosmarium sp X Crucigenia tetrapedia (Kirchner) W. West & G.S. West 1902 Eudorina sp X Kirchneriella contorta (Stearn 1973) X Oocystis sp X Scenedesmus acuminatus (Lagerheim) Chodat 1902 X Scenedesmus quadricauda (Turpin) Brébisson sensu Chodat, 1913 X X X X Schroederia setigera (Schröder) Lemmermann 1898 X Selenastrum sp X Cianophyceae Anabaena sp X X Calothrix sp X X Chroococcus turgidus (Kützing) Nägeli 1849 X X Cylindrospermopsis raciborskii (Woloszynska) Seenayya and Subba Raju X X Gloetrichia sp X Lyngbya sp X X X Mycrocistis sp Oscillatoria sp X X Planctothrix sp X X Euglena sp X X Phacus sp X Strombomonas sp X Trachelomonas sp X Euglenophyceae X Zooplâncton Rotifera Bdelloidea sp X X Brachionus falcatus (Zacharias, 1898) Lecane sp X Lecane stenroosi (Meissner, 1908) X Não identificado X Ceriodaphnia cornuta (Sars, 1886) X Diaphanosoma spinulosum (Herbst, 1967) X Moina minuta (Hansen, 1899) X Náuplio X X Cladocera X Copepoda Não identificado Conchostraca X X X X 184 Ostracoda X Nematoda X Oligochaeta X X Família Glossiphoniidae X Insect remains X X Família Athericidae Família Chiromidae (pupa) Família Chironomidae (larva) X X X X Scales TOTAL A Food diet of S. notonota preserved with formalin in the field This sample showed a diet composed by 59 item, being 35.6 % exclusive of it: Chironomidae, Cymbella sp, Diploneis sp, Ephitemia sp, Eunotia sp, Neidium sp, Eudorina sp, Kirchneriella contorta, Scenedesmus acuminatus, Scenedesmus quadricauda, Gloetrichia sp, Phacus sp, Strombomonas sp, Bdelloidea sp, Lecane 59 49 setenroosi, Diaphanosoma spinulosum, Copepoda (Náuplio), Moina minuta, Oligochaeta, fish scale and Ostracoda. The more frequent food item in the studied species were: detritus, vegetable rests, Bacyllariophyceae, Chlorophyceae, being present in 100% of the guts, followed by zooplankton (Cladocera and Copepoda, 90% each), eggs and Cyanophyceae (both 80%), Nematoda, Conchostraca, Ostracoda and Rotifera 60% each. (Fig.2). 100 Frequência de ocorrência (%) 90 80 70 60 50 40 30 20 10 Re De s t Re tos r ito ve s st os ge de tai in s s Se etos m en te Ba s cy lla O rio vo Ch p hy s c lo ro eae Ci p hy an ce Eu op ae h gl en yc e a op hy e ce a Ro e tif e Cl a d ra oc Co era pe p Ne o d m a at od E a Co sc a nc ma ho s st ra O s t ca ra c O lig o da oc ha et a 0 Fig. 2 – Frequency of occurrence of food diet of S. notonota from the sample preserved in field with formalin 10% In different species of Steindachnerina, Giora & Fialho (2003) and Melo et al. (2004), observed similar food diets as the present species with the preferential food item being detritus. But on first study, analyzing S. brevipinna, the authors identified other associated item like Diatomaceae, Desmidiacea and other Chlorophyceae and Protozoa, and on the second study analyzing S. aff. Elegans, the authors identified only vegetable remains 185 associated with detritus. Nevertheless, detailed studies about food diet of S. notonota are scarce, making difficult other comparisons about this subject. Food diet of S. notonota preserved in ice in the field The guts analyzed by this method revealed a less varied diet, being composed by 49 item, from these 24.5 % occurred only in this sample: Athericidae (Diptera), Glossiphoniidae (Hirudínea); microalgas: Cocconeis sp, Rhopalodia sp, Cosmarium sp, Acnanthes sp, Caloneis bacillum, Crucigenia tetrapedia, Schroederia setigera, Selenastrum sp, Mycrocistis sp; e zooplâncton: Brachionus falcatus. The more frequent food item preserved by this method were: Bacyllariophyceae, Chlorophyceae, being these present in 100 % of the guts, followed by vegetable remains 90 %, eggs and Cianophyceae 80% each. The zooplankton food , represented by Cladocera and Copepoda presented a low frequency of occurrence, comparing with the other sample preserved with formalin in the field (Fig. 3). The mean frequency of the food item in guts in the sample preserved with formalin in the field was superior to the sample frosty in the field, 22.1±6.7 and 13.6±5.3, respectively, showing statistic significant differences among diets (t = 3,82; p < 0,01). 100 Frequência de ocorrência (%) 90 80 70 60 50 40 30 20 10 R es D e R tos trit es ve os to ge s de ta i in s se to s S em en B te ac s yl la rio O ph vo C yc s hl ea or e op hy C c ia ea no e E ug ph yc le no e ph ae yc ea e R o tif er C a la do ce C op ra C e o nc po ho da st ra ca 0 Fig. 3 – Freqüência de ocorrência dos itens alimentares na dieta de S. notonota da amostra cujos estômagos foram previamente congelados. Comparing our results with others found by Teixeira & Gurgel (2004), about the nutrition dynamics of S. notonota in Riacho da Cruz (RN) Dam, which sample was frosty in the field, we can observe that its diet is similar of this work in many item as: detritus, algae (Chlorophycea, Cianophyceas, Diatoms and Euglenophycea) and rotífers, excepting tecamebas, Desmidiacea and inorganic sediment. Following the same author, sediment, diatoms and detritus were frequent in 100 % of the analyzed guts, being followed by rotifers and Chlorophycea in frequency of occurrence of 81.82% e 78.79%, respectively. 186 Considerations about the food diet of S. notonota According with Luz (2001), the great trophic plasticity presented by tropical water fishes is the reflection between quality and quantity of available food in the environment, and the restriction morphological-behavior degree exhibited by species, being the latter subordinated to ontogenetic variations. This plasticity following the same author make easy the establishment of this species in closed lagoons, where great environmental fluctuations are expected, affecting the availability of food, as we can observe in paraiban semi arid aquatic environments. The food diet of the study species, who has the habit of feed on detritus, independent of the methods applied, presented few recognized items in a macroscopic observation, as observed in the gut contents of detritus feeder species analyzed by Mérona & Rankin-DeMerona (2004), showing the importance of the microscopic analyzes in the food diet studies in detritivorous fishes. The item food coming from samples frosty presented a bad conservation and mostly of the difficult identification, confirming what was found for Zavala-Camin (1996), that the frozen, decrease, but do not stop the digestive process. The reverse was observed in formalin samples which presented a better preservation, allowing the identification of a higher number of the food item. The analyzes of the food diet of S. notonota following the two methodologies, in the present study, demonstrated that detritus has an important part in the species diet as observed earlier by Hahn et al. (1997), this item was important in the diet of 18.7 % of the analyzed species in the Segredo – Paraná Reservoir. The same was observed in the detritivorous fishes of the Paraná River floodplain, which ingest great quantity of thin and thick particles together with microorganisms and unicellular algae (HAHN et al. 2003). Independent of the applied methodology detritus, vegetable remains Bacyllariophyceae and Clorophyceae in all analyzed fishes. CONCLUSIONS This species presented a diet specially detritivorous associated with vegetable remains, Bacyllariophyceae and Chlorophyceae. 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