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Brazilian Archives of Biology and Technology

Print version ISSN 1516-8913On-line version ISSN 1678-4324

Braz. arch. biol. technol. vol.48 no.3 Curitiba May 2005

http://dx.doi.org/10.1590/S1516-89132005000300013 

BIOLOGICAL AND APPLIED SCIENCES

 

Biology of Chirocentrodon bleekerianus (Poey, 1867) (Clupeiformes: Pristigasteridae) in a continental shelf region of southern Brazil

 

 

Carlos Eduardo CorrêaI; Paulo de Tarso ChavesII, *; Paulo Ricardo Bittencourt GuimarãesIII

IDepartamento de Engenharia Florestal; UNICENTRO; Irati - PR - Brazil
IIDepartamento de Zoologia; Universidade Federal do Paraná; Centro Politécnico; Jardim das Américas; C. P. 19020; .ptchaves@ufpr.br 81531-980; Curitiba - PR - Brazil
IIIDepartamento de Estatística; Universidade Federal do Paraná; Curitiba - PR - Brazil

 

 


ABSTRACT

This study provides information on the biology of C. bleekerianus from Paraná State coast, Brazil, assembling data about its abundance, size structure, diet and reproduction. Monthly collections were accomplished in 1999 and 2000 in the internal continental shelf, with trawl net. The catch-per-unit-effort did not vary significantly among the seasons. In the summer, the individuals were larger, followed by autumn, spring and winter. C. bleekerianus was predominantly planktivorous and the most frequent items in its diet were copepods followed by diatomaceous algae. Seasonal variation in the frequency values of the gonad maturation stages, gonadossomatic index and gonadal condition factor indicated that the reproductive period encompassed spring and summer. The mean total length at first maturity of females was estimated to be 76 mm.

Key words: Abundance, Brazil, Chirocentrodon, Clupeiforms, feeding, reproduction


RESUMO

Este trabalho fornece dados sobre a biologia de C. bleekerianus do litoral do Estado do Paraná, reunindo dados sobre sua abundância, estrutura em tamanho, dieta e reprodução. Coletas mensais foram realizadas em 1999 e 2000 na plataforma continental interna, com rede de arrasto de fundo com portas. A captura por unidade de esforço não variou significativamente entre as estações do ano. No verão os indivíduos eram maiores, seguido do outono, primavera e inverno. C. bleekerianus é predominantemente planctívora, sendo copépodos seguidos de algas diatomáceas os itens alimentares mais freqüentes em sua dieta. As variações sazonais de valores da freqüência de estádios de maturação gonadal, do índice gonadossomático e do fator de condição gonadal indicam que o período reprodutivo compreende primavera e verão. O comprimento total médio de primeira maturação das fêmeas é estimado em 76 mm.


 

 

INTRODUCTION

In a survey carried out by Chaves et al. (2001) it was observed that in the region of the internal continental shelf of Paraná State during the years 1999 to 2000, Chirocentrodon bleekerianus was one of the most abundant species (16.5% in number and 4.5% in biomass). This species is also common in the region of Paranaguá Bay and the adjacent beaches of Shangri-lá and Leste, and areas that are further away from the coast (close to the Currais islands) (Corrêa, 1987).

With the exception of the genus Ilisha, the individuals of which reach 70 cm in length, the family Pristigasteridae is made up of small sized fish, and consequently show little economic value as fishing resources (Whitehead, 1985; Cérvigon et al., 1992). The Pristigasteridae form schools and inhabit coastal waters, commonly entering bays and estuaries (Figueiredo and Menezes, 1978; Whitehead, 1985). It is known that they represent a wide portion of the diet of many pelagic species of commercial importance, as well as birds and marine mammals (Crawford et al., 1992; Friedlander and Beets, 1997). C. bleekerianus reaches 12 cm in total length, has a silverish stripe on its side, distributed range from Panama to off Rio Grande do Sul State, Brazil (Figueiredo and Menezes, 1978), and is found at depths of up to 40 m (Cérvigon et al., 1992).

In spite of the extensive literature on taxonomy, fishing and biology regarding the Clupeiformes (Whitehead, 1985), many genera are still not very well known, mainly the tropical and subtropical ones (Blaber et al., 1998), as is the case of Chirocentrodon. This study aims to supply data about abundance, size structure, feeding and reproduction of C. bleekerianus in a region of the internal continental shelf of southern Brazil.

 

MATERIAL AND METHODS

The study area is located on the Paraná coast, South of Brazil (25º45'S;48º20'W). Its climate is humid subtropical; the mean temperature oscillating from 17ºC in the coldest month to 24ºC in the warmest month (Bigarella, 1978). The water, however, usually shows lower temperatures, due to the influence of sub-Antarctic currents, rich in nutrients (Brandini, 1990).

The collections were carried out monthly, between March 1999 and January 2000 (except in September), at depths of 10 and 15 meters, using trawl net (mesh size 20 mm). Three bottom-trawls of 10 minutes each were used at each depth, totalizing six trawls per month, always in the morning. Individuals from an area close to the experimental collections were acquired in the fish market of Guaratuba, in January 2002, in order to obtain additional material for the accomplishment of the study on the length at first maturity.

The fishes were identified, counted and measured for total length (LT) and total weight (WT). Stomachs were removed and preserved in 4% formaline for content identification. The sex and maturation stage were recognized macroscopically according to the Vazzoler (1996) scale, and gonads were weighed (WG).

The monthly catch-per-unit-effort was calculated, in number of individuals - CPUEn and in biomass - CPUEg, being the unit effort the trawl time, in minutes. The data were log transformed and the mean values compared among seasons (spring: October, November and December, and so forth). For evaluating the seasonal differences, the tests of analysis of variance (one-way ANOVA) with µ=0.05 and Tukey-Kramer were used. Barlett's test was used to verify data homocedasticity.

Seasonal distribution in size of the individuals was evaluated using the non-parametric statistical test of Kolmogorov-Smirnov, with µ=0.05.

The diet was characterized based on the stomach content, using the Frequency of Occurrence (F.O.) method of Hynes (1950). To evaluate the similarities in the diet throughout the seasons, a cluster analysis was made based on a similarity matrix, built with the use of the Jaccard coefficient. To evaluate differences in F.O. of the main food items between young and adults, the c2 test of independence was used, with µ=0.05, where all the individuals that had gonads in stages B - in maturation or C - mature, were considered to be adults.

To detect seasonal differences in the sex ratio, the test c2 of independence was used, with µ=0.05. As the amount of males obtained was small, the indicators of spawning periods and size of first maturation were only calculated for females. Seasonal averages of: Gonadossomatic Index, GSI=WG/WT x 100 (i); Gonadal Condition Factor (ii), DK=WG/LTb, being "b" the angular coefficient of length/weight relationship; and seasonal frequency of gonadal maturation stages (iii) were calculated (Vazzoler, 1996). The c2 test of independence was used, with µ=0.05, to estimate the frequencies of gonadal maturation stages dependence according to season. The reproductive period was estimated by analyzing the mean seasonal variation of the values of (i), (ii) and (iii). The length at first maturity was determined through the curve that relates the mean point of the TL classes to the relative frequency of the adult individuals (with gonads from the B stage). For the adjustment of this curve, the following equation was used:

Fr=1-e-aLt exp b; where: Fr= relative frequency of adult females, e= base of the neperian logarithm, a and b= coefficients linear and angular of length/weight relationship and Lt= medium point of the total length classes.

 

RESULTS

The largest values of CPUEn and CPUEg were detected in the spring, while the smallest ones occurred in the summer (Fig. 1). However, in terms of mean values, there were no significant differences between seasons either in number of individuals (F=0.95; DF=3; p>0.05), or in biomass (F=0.68; DF=3; p>0.05).

 

 

The non-parametric test of Kolmogorov-Smirnov showed that size distributions were different among seasons: there were larger individuals in summer, followed by autumn, spring and winter (Fig. 2). In spring, most of the captured individuals belonged to the intermediary length classes (80-99 mm) and in summer, to intermediary and large length classes (85-109 mm) (Fig. 2). In autumn and winter most of the captured individuals belonged to the small and intermediary length classes (70-99 mm) (Fig. 2).

 

 

Copepoda, followed by Diatomacea algae, were the more frequent food items in the diet of the species, followed by fish, Amphipoda, Crustacea larvae, non-Brachyura Decapoda and Mysidacea. Except for the former, these items occurred in all the seasons (Table 1). Three items reached the largest frequency values: Copepoda throughout the year, fish in summer and autumn, and Diatomacea algae in autumn (Table 1). The diet of the individuals collected in spring, winter and autumn presented a similarity of 85.7%, whilst that of the individuals collected in spring and winter had a similarity of 100%. Between summer and the other seasons, the similarity was of 52% (Fig. 3).

 

 

 

 

The occurrence frequency of the non-identified Crustacea and Copepoda items was significantly larger in the young individuals than in adults; on the other hand, the F.O. of the fish item was significantly larger in the adult individuals (Fig. 4).

 

 

With the exception of autumn, significant differences in the sex ratio occurred in all other seasons, being that in spring and summer a larger proportion of females was observed and in winter the opposite occurred (Fig. 5). The frequencies of gonadal maturation stages were dependent on the season (c2=94.01; DF=6; p<0.05). Mature individuals (stage C) occurred with a larger frequency in spring and summer and immature individuals (stage A) occurred with a larger frequency in autumn and winter (Fig. 6). In the present study, individuals with emptied gonads were not found.

 

 

 

 

Both the GSI and the DK presented larger values in spring and in summer (Fig. 7 and 8).

 

 

 

 

Based on the frequencies of gonadal maturation stages, GSI and DK, the reproductive period of the species in that region can be estimated to extend from spring to summer. The length at first maturity (L50) estimated for the females, was 76 mm. The mathematical equation of the linear transformation of the maturation curve is Y=5.81X - 25.77 (n= 364; R2= 0.80), being the curve of first maturation adjusted by the equation Fr = 1 - e -10EXP -11. 76 Lt EXP 5.81.

 

DISCUSSION

The Clupeiformes are pelagic fish, therefore, it would be unlikely that large numbers would be captured using bottom-trawl nets. However, there are records of abundant occurrence of Chirocentrodon bleekerianus in other regions with similar fishing modalities (Manickchand-Heileman and Julien-Flus, 1990). In the internal continental shelf of Paraná State, the high capture of this species is possibly being favored by low depth of the area, an adverse condition for a stratified distribution.

The largest capture in the study area occurred in spring and the smallest in summer. Other studies (Maravelias and Reid, 1995; Power et al., 2000; Corten, 2001) stated that in certain regions, Clupeiformes were more abundant during periods of high temperatures. Nevertheless, in the internal continental shelf of Paraná State, the smallest capture values occurred in summer. As the decrease in capture coincides with the progress of gonadal maturation, the low numbers could suggest a probable migration of the species from the area in order to spawn elsewhere.

With regard to the distribution of size classes, the capture of bigger individuals in summer could be associated to the largest concentration of adults close to spawning. This has been reported for another Clupeiformes in Mexico (García-Abad et al., 1998) and in Chile (Cubillos et al., 2001).

Based on the items found in the stomach content of C. bleekerianus, the species could be classified as predominantly planktivorous, which is common amongst Clupeiformes (James, 1988). Seasonal changes in the diet are generally a consequence of the actual availability of food (Zavala-Camin, 1996).

The values of the Jaccard coefficient indicated high similarity in the diet of C. bleekerianus between autumn, winter and spring. However, the coefficient was qualitative, which meant that it only evaluates the presence and absence of food items in common between the seasons, without considering the relative abundance of the items in the stomach content.

A variation of the food items according to size was observed and, whereas copepods were significantly more frequent in the diet of juveniles, fishes were significantly more frequent in the diet of adults. Changes in the diet relative to size are common in fish, being that the main change is in the actual size of the items eaten, which may or may not influence a change in the nature of the food (Zavala-Camin, 1996). Changes in the diet according to size have been related to ontogenetic changes that occur in the digestive tract of the fish (Kaiser and Hughes, 1993).

C. bleekerianus presented a larger proportion of females in the spring in relation to males, a fact that, according to García-Abad et al. (1998), could represent an adaptive strategy of the species to have a larger stock of eggs and therefore a larger recruitment of young. In another species of tropical Clupeiformes, a larger proportion of females was also observed (García-Abad et al., 1998; García-Abad et al., 1999).

The high frequencies of mature females in the spring and summer and the high values of the Gonadossomatic index and of the Gonadal Condition factor in these seasons, indicated that the reproductive period of the species occured at this time. As females with emptied ovaries were not found in the present study, and because the species was not found in shallower areas than those of the present study (Godefroid, 1997, 2002; Corrêa, 1987; Chaves and Corrêa, 1998; Chaves and Vendel, 2001), it was possible that spawning occured at depths more than 15 meters.

More studies on the biology of C. bleekerianus, as well as of other species of Clupeiformes, are necessary for a better understanding of the ecosystems where they occur, since they are, as a rule, abundant species. Such studies could contribute to the elaboration of more complete management plans for these environments.

 

REFERENCES

Bigarella, J. J. (1978), A Serra do Mar e a Porção Oriental do Estado do Paraná. Secretaria de Estado do Planejamento/Associação de Defesa e Educação Ambiental, Paraná. 248 pp.        [ Links ]

Blaber, S. J. M.; Staunton-Smith, J.; Milton, D. A.; Fry, G.; Van Der Veld, T.; Pang, J.; Wong, P. and Boon-Teck, A. (1998), The biology and life-history strategies of Ilisha (Teleostei: Pristigasteridae) in coastal waters and estuaries of Sarawak. Estuarine, Coastal and Shelf Science, 47, 499-511.        [ Links ]

Brandini, F. P. (1990), Hidrogeography and characteristics of the phytoplankton in shelf and oceanic waters off southeastern Brazil during winter (July/August 1982) and summer (February/March 1984). Hydrobiologia, 196, 111-148.        [ Links ]

Cérvigon, F.; Cipriani, R.; Fischer, W.; Garibaldi, L.; Hendrickx, M.; Lemus, A. J.; Márques, R.; Poutiers, J. M.; Robaina, G. and Rodriguez, B. (1992), Guia de Campo de las Especies Comerciales Marinas y de Aguas Salobres de la Costa Septrentional de Sur America, Roma. 513 pp.        [ Links ]

Chaves, P. T. C. and Corrêa, M. F. M. (1998), Composição ictiofaunística da área de manguezal da Baía de Guaratuba, Estado do Paraná, Brasil (25°52'S; 48°39'W). Revista Brasileira de Zoologia, 15 : (1), 195-202.        [ Links ]

Chaves, P. T. C.; Grando, G. C. and Calluf, C. C. (2001), Ictiofauna demersal de um trecho de plataforma interna no Paraná: variações temporais e aspectos reprodutivos. In: Semana Nacional de Oceanografia, 14., Rio Grande : Centro Acadêmico Livre de Oceanologia. CD-ROM.        [ Links ]

Chaves, P. T. C. and Vendel, A. L. (2001), Nota complementar sobre a composição ictiofaunística da Baía de Guaratuba, PR, Brasil. Revista Brasileira de Zoologia, 18 : (Supl. 1), 349-352.        [ Links ]

Corrêa, M. F. M. (1987), Ictiofauna da Baía de Paranaguá e adjacências (litoral do Estado do Paraná - Brasil). Levantamento e produtividade. Dissertação de Mestrado, Universidade Federal do Paraná. 406 pp.        [ Links ]

Corten, A. (2001), Northern distribution of North Sea herring as a response to high water temperatures and/or low food abundance. Fisheries Research, 50: 189-204.        [ Links ]

Crawford, R. J. M.; Undrhill, L. G.; Raubenheimer, C. M.; Dyer, B. M. and Martin, J. (1992), Top predators in the Benguela ecosystem - implications of their trophic position. South African Journal of Marine Science, 11, 675-687.        [ Links ]

Cubillos, L. A.; Arcos, D. F.; Bucarey, D. A. and Canales, M. T. (2001), Seasonal growth of small pelagic fish off Talcahuano, Chile (37º S, 73º W): a consequence of their reproductive strategy to seasonal upwelling? Aquatic Living Resources, 14, 115-124.        [ Links ]

Figueiredo, J. L. and Menezes, N. A. (1978), Manual de Peixes Marinhos do Sudeste do Brasil. II. Teleostei (1). São Paulo : Museu de Zoologia-USP. 110 pp.        [ Links ]

Friedlander, A. M. and Beets, J. P. (1997), Fisheries and life history characteristics of dwarf herring (Jenkinsia lamprotaenia) in the US Virgin Islands. Fisheries Research, 31, 61-72.        [ Links ]

García-Abad, M. C.; Tapia-García, M.; Yáñez-Arancibia, A. and Sánches-Gil, P. (1999), Distribuición, abundancia y reprodución de Harengula jaguana Goode y Bean, 1879, en la plataforma continental del sur del Golfo de México (Pisces: Clupeidae). Biotropica, 31(3): 494-501.        [ Links ]

García-Abad, M. C.; Yáñez-Arancibia, A.; Sánches-Gil, P. and Tapia-García, M. (1998), Distribuición, abundancia y reprodución de Opistonema oglinum (Pisces: Clupeidae) en la plataforma continental del sur del Golfo de México. Revista de Biologia Tropical, 46 : (2), 257-266.        [ Links ]

Godefroid, R. S. (1997), Estrutura da comunidade de peixes da zona de arrebentação da praia de Pontal do Sul, Paraná, Brasil. Dissertação de Mestrado, Universidade Federal do Paraná, 130 pp.        [ Links ]

Godefroid, R. S. (2002), A composição e a estrutura de peixes em ambientes rasos. Tese de Doutorado, Universidade Federal do Paraná, UFPR. 144 pp.        [ Links ]

Hynes, H. B. N. (1950), The food of freshwater sticklebacks (Gasterosteus aculeatus and Pygosteus pungiatus), with a review of methods used in studies of the food of fishes. Journal of Animal Ecology, 19 : (1), 36-58.        [ Links ]

James, A. G. (1988), Are clupeid microphagists, herbivorous or omnivorous? A review of the diets of some commercially important clupeids. South African Journal of Marine Science, (7), 161-177.        [ Links ]

Kaiser, M. J. and Hughes, R. N. (1993), Factors affecting the behavioural mechanisms of diet selection in fishes, pp. 105-118. In: Huntingford, F. A. and Torricelli, P. (Eds.). Behavioural Ecology of Fishes. Proceedings of a conference held at Ettore Majorana Centre for Scientific Culture, Italy.        [ Links ]

Manickchand-Heileman, S. and Julien-Flus, M. (1990), Species composition and seasonality of a coastal demersal fish stock in Trinidad, West Indies. Caribbean Marine Studies, 1 : (1), 11-21.        [ Links ]

Maravelias, C. D. and Reid, D. G. (1995), Relationship between herring (Clupea harengs, L.) distribution and sea surface salinity and temperature in the northern North Sea. Scientia Marina, 59 : (3-4), 427-438.        [ Links ]

Power, M.; Attrill, M. J. and Thomas, R. M. (2000), Temporal abundance patterns and growth of juvenile herring and sprat from the Thames estuary 1977-1992. Journal of Fish Biology, 56, 1408-1426.        [ Links ]

Vazzoler, A. E. A. de M. (1996), Biologia da Reprodução de Peixes Teleósteos: Teoria e Prática. Maringá : EDUEM - SBI. 169 pp.        [ Links ]

Whitehead, P. J. P. (1985), FAO Species Catalogue 7, Clupeoid Fishes of the World. Part I - Chirocentridae, Clupeidae and Pristigasteridae. vol. 7, Part 1, FAO Fisheries Synopsis 125. 303 pp.

Zavala-Camin, L. A. (1996), Introdução aos Estudos Sobre Alimentação Natural em Peixes. Maringá : EDUEM - SBI. 129 pp.        [ Links ]

 

 

Received: November 17, 2003;
Revised: April 01, 2004;
Accepted: September 17, 2004.

 

 

* Author for correspondende

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