Ovarian development and spawning of Serra Spanish mackerel in coastal waters of Northeastern Brazil

Desenvolvimento ovariano e desova da Serra nas águas costeiras do nordeste do Brasil

Ovarian development and spawning of Serra Spanish mackerel in coastal waters of Northeastern Brazil

Desenvolvimento ovariano e desova da Serra nas águas costeiras do nordeste do Brasil

Chellappa, S.^I,*; Lima, JTAX.^II; Araújo, A.^II; Chellappa, NT.^I

^IPrograma de Pós-Graduação em Ecologia, Departamento de Oceanografia e Limnologia, Centro de Biociências, Universidade Federal do Rio Grande do Norte – UFRN, CEP 59072-970, Natal, RN, Brazil

^IIPrograma de Pós-Graduação em Psicobiologia, Departamento de Fisiologia, Centro de Biociências, Universidade Federal do Rio Grande do Norte – UFRN, Av. Salgado Filho, 3000, Lagoa Nova, CEP 59072-970, Natal, RN, Brazil

ABSTRACT

The Serra Spanish mackerel, Scomberomorus brasiliensis is an important fishery resource of the Atlantic Ocean and is a major component of artisanal fisheries in northern and northeastern Brazil. Ovarian development and spawning period of S. brasiliensis were investigated using both macroscopic and histological techniques. Mean monthly values of GSI and ovarian maturation indicate that the main spawning period occurs during the rainy season.

Keywords: Serra Spanish mackerel, spawning period, ovarian development, histology, GSI.

RESUMO

A Serra, Scomberomorus brasiliensis, é uma espécie marinha de valor comercial do oceano Atlântico sendo um maior componente de pesca artesanal no norte e nordeste brasileiros. Desenvolvimento ovariano e época de desova de S. brasiliensis foram investigados utilizando-se técnicas macroscópicas e histológicas. Valores mensais médios de IGS e maturação gonadal indicam que a época de desova ocorre durante o período de chuva.

Palavras-chave: Serra, época de desova, desenvolvimento ovariano, histologia, IGS.

1. Introduction

The Serra Spanish mackerel, Scomberomorus brasiliensis (Collette, Russo and Zavala-Camin) (Osteichthyes: Scombridae) occurs in the Western Atlantic, along the Caribbean in Central Atlantic coasts and Southwest Atlantic from Belize to Rio Grande do Sul, Brazil (Collette et al., 1978). It is an important fishery resource of the Atlantic Ocean and is a major component of artisanal fisheries in northern and northeastern Brazil, with high commercial value. Although the importance of S. brasiliensis throughout most of its distributional range is considered vital, limited details are available regarding the gonadal development of this species. Some aspects of the reproductive biology of S. brasiliensis have been studied throughout its geographical range. Information on ovarian maturity required for stock assessments, is insufficiently described in the available literature which is mostly restricted to Ceará state in northeastern Brazil (Gesteira and Ivo, 1973; Ximenes, 1981; Fonteles-Filho, 1988; Lucena et al., 2004).

Estimates of absolute and relative fecundity have been made (Gesteira, 1972; Gesteira and Mesquita, 1976; Lima et al., 2007). Studies conducted in the western coast of Maranhão, Brazil, indicate that the reproductive period of S. brasiliensis extends from June to November, with the participation of 3 year old females which attain sexual maturity at 411 mm and 4 year old males at 443 mm (Lima, 2004). In coastal waters of Rio Grande do Norte, females of S. brasiliensis attain gonad maturity at 280 mm and males at 345 mm of total body length (Lima et al., 2007).

However, understanding of the reproductive biology in Serra Spanish mackerel is complicated by the distribution of the population and most information has been gathered from spatially and temporally restricted periods. A complete description of the reproductive cycle of S. brasiliensis including oogenesis and spawning strategy has not been documented. Thus, a number of basic questions could be asked about the Serra Spanish mackerel population in the coastal waters of northeastern Brazil. For example, do they exhibit an annual variation in the gonadosomatic index? Do they exhibit synchronous or asynchronous spawning? Is their spawning season modulated by environmental factors?

The objective of this study was to provide a comprehensive description of the macroscopic and histological aspects of ovarian maturation of Serra Spanish mackerel, S. brasiliensis of the Atlantic Ocean coastal waters of northeastern Brazil. This study also examines the annual variation in the gonadosomatic index focusing on spawning season. Investigation was made to correlate the spawning season of this species with rainfall, one of the environmental factors known to modulate the duration and timing of the spawning period of tropical fish.

2. Material and Methods

2.1. Study area and sample collection

During the period of September 2005 to August 2006, monthly samples of Serra Spanish mackerel, S. brasiliensis were collected from artisanal fisheries at various locations in the coastal waters of Rio Grande do Norte, Brazil, situated between latitudes 56° 44' and 5° 52' S, longitudes 35° 09' and 35° 12' W. The samples were randomly collected from catch landed by fisherman. Fish were caught by local fishermen using beach-seines from the coastal waters of approximately <10 m depth. The beach-seines were 110 m in length, 3 m in height, with a mesh size of 1 cm in the central part and 7 cm in the extremities. Fish collected from the beach-seine were numbered, measured, weighed and samples of whole fish were used for morphometric analysis to confirm the taxonomical identification of the species (Carpenter, 2002). Rainfall data of the region was obtained from the Meteorological Department of Natal, Brazil.

2.2. Measurements

A total of 826 fish was collected during the study period. The total body length (Lt) of fish were measured to the nearest 1 mm and body mass (Wt) recorded (±1 g). Fish were dissected within a few hours of capture, and gonads were removed, weighed (Wg ± 0.1 mg) and examined to separate the sex. A total of 402 females collected were separated for detailed studies.

2.3. Macroscopic and histological examinations of ovaries

The location and general aspects of the ovaries were noted and stage of reproductive maturity determined using a macroscopic staging system. The ovaries were classified as Immature (small ovaries without visible oocytes), Maturing (ovaries occupying ¼ to ¾ of body cavity, with visible opaque oocytes), Mature (large ovaries almost occupying the entire body cavity with blood capillaries), Spent (flaccid ovaries and purple in colour) (Mackie and Lewis, 2001). Turgidity, colour and presence of blood vessels of the ovaries were also observed. In order to avoid possible variation in the developmental stage of oocytes due to their position in the ovaries, histological examinations were carried out on sections from the anterior (cephalic), middle (central), and posterior (caudal) regions of 20 ovaries in different developmental stages (Yoshida, 1964).

These data were later compared in order to determine whether samples taken from mid-section of the ovary of either lobe were representative of oocyte development. The gonads were preserved in Bouin's solution, later embedded in paraffin, sectioned at 3-5 mm thickness, and stained with Harris Hematoxylin and Eosin (H&E).

Ovarian developmental stages were assessed microscopically with the help of light microscope (Taimin, model TM 800), coupled with a video camera (Kodo Digital). The terminology used for stages of oogenesis followed that of West (1990) and Palmer et al. (1995).

2.4. Estimation of gonadosomatic index and spawning period

The gonadosomatic index (GSI) was calculated using the formula of Wootton et al. (1978): GSI = weight of ovary (g) / body weight of fish (g) - weight of gonads (g) × 100. Period of breeding was determined by the temporal relative frequency distribution of the different stages of ovarian maturation (De Martini and Fountain 1981).

2.5. Statistical analyses

Distributions of raw data were checked for normality and were normal log transformed when necessary. Length-weight relationships were determined using logarithmically transformed data. Pearson's correlation tests were performed to determine the correlation between the variables weight and length. Gonadosomatic indices of females during rainy and dry periods were compared at 5% level using Mann-Whitney U test. The software package SPSS for Windows 13.0 was used for all statistical analyses.

3. Results

3.1. Rainfall

During the study period rainfall varied from a minimum of 1.2 mm in November, 2005 to a maximum of 427.9 mm in April, 2006 (138.9 ± 135.9). Northeastern Brazil experienced 5 months of drought from September to January (21.3 ± 17.4), and 7 months of rain from February to August (206.7 ± 128.1).

3.2. Total body length and weight

Amplitude of total body length (Lt) of sampled females over the whole year varied from 93 to 805 mm (289.2 ± 153.4). During the drought period, their total body length ranged from 107 to 805 (312.2 ± 176.5), and during the rainy season from 93 to 565 mm (275.0 ± 135.9). A higher frequency of occurrence of females in the class intervals 100 to 200 mm. of total body length was registered throughout the year. The amplitude of total body weight (Wt) of the females varied from 8.1 to 3385 g (265.6 ± 430.9) over the year. During the drought period, total body weight of females varied from 8.1 to 4390 g (382.4 ± 692.5) and during the rainy season from 11 to 1015.8 g (206.5 ± 250.9). A higher frequency of occurrence of females in the class intervals 8 to 500 g of body weight was observed throughout the year.

The amplitude of gonad weight (Wg) varied from 0.005 to 119.99 g (2.97 ± 0.72) over the year. Figure 1 shows the positive correlations between body mass and length (r² = 0.959; P < 0.0001), and between gonad weight and body mass (r² = 0.836; P < 0.0001) of females S. brasiliensis.

3.3. Macroscopic and histological aspects of ovaries

The ovaries were bi-lobed, elongated, and joined posteriorly to form a short gonoduct leading to the urogenital pore. The macroscopic staging of ovaries based on the external appearance showed four stages: immature, maturing, mature and spent, conforming with the literature used for the methodology (Figure 2). Classification and description of the macroscopic aspects of ovarian development stages are given in Table I.

Figure 3 shows the monthly frequency of ovarian maturity stages in S. brasiliensis during the study period.

Microscopic examination of ovarian sections showed that the oocyte development was consistent along the whole length of the ovary depending on the degree of maturation. Ovaries revealed five stages of oocyte development: immature, early stage of maturing, late stage of maturing, mature and spent (Table 1, Figure 4).

3.4. Gonadosomatic Index (GSI)

GSI of females varied from 0.02 to 7.14 (0.34 ± 0.91). Monthly values of GSI of maturing, mature and spent females showed reproductive activity from March to June. In April adult females (n = 4) had GSI varying from 0.14 to 3.24 (1.69 ± 1.78) and in June (n = 16) from 0.08 to 4.14 (1.10 ± 1.81) (Figure 5). Reproductive activity occurred during the rainy season which lasted from February to August. During the rainy period, GSI of females varied from 0.02 to 4.14 (0.27 ± 0.67) and during the dry season, GSI ranged from 0.02 to 7.14 (0.46 ± 1.19). The highest GSI (7.14) of females in November was due to one mature individual. The differences in the mean values of GSI in drought and rainy periods showed significant difference (P < 0.001) (Figure 5).

3.5. Spawning period

Large mature females had on an average a total body length of 712.7 mm (± 117.3) and weight of 2476.9 g (±1043.82), with ovaries on an average weighing 71.3 g (±36.8). Mature ovaries showed the reserve stock of perinucleolar stage oocytes (phase II) with diameter size <120 mm and mature oocytes with diameters ranging from 600 to 750 µm. Evidence of spawning was found in the histologically processed ovaries. The peak reproductive activity occurred during March to June, coinciding with the rainy season which lasted from February to August.

4. Discussion

The present study documents the changes in the ovarian activity and spawning in Serra Spanish mackerel occurring in the coastal waters of Rio Grande do Norte in northeastern Brazil. Growth of females in weight reflects the reproductive cycle, as the ovaries mature they increase in weight which adds to the total weight of fish. Differences in growth patterns of females can thus provide a mechanism for an adaptive phenotypic response to changes in tropical coastal environments.

The onset of sexual maturity represents a critical transition in the life history, since resource allocation is related mainly to growth before and to reproduction after sexual maturity (Potts and Wootton, 1984; Chellappa et al., 1995). The present study establishes four macroscopic stages and five stages of ovarian oocyte development for females of Serra Spanish mackerel. The macroscopic classification and histological analyses of the ovaries suggest that there is a regular pattern of gonadal development for each maturity stage, such as the immature, developing, mature and spent stages. An earlier study has revealed the ovarian developmental stages for the narrow-barred Spanish mackerel, Scomberomorus commerson, in Western Australia (Mackie and Lewis, 2001) and a similar pattern was observed in the present study.

The reproductive process, such as gonad maturation, in tropical fishes is influenced by various environmental changes induced by the onset of rains. Drought is a natural climatic situation which is characteristic of northeastern Brazil, with an irregular pattern of distribution of rain in the region. The spawning characteristics of females of Serra Spanish mackerel showed that the peak period of reproductive activity was during March-June coinciding with the rainy season and very few spawning fish were found outside these months. The macroscopic and histological analysis of ovaries equally confirmed that breeding season commenced with the onset of rains.

In tropical regions the rainfall plays an important role in determining the reproductive cycles of fishes and collective reproduction occurs during the time when environmental conditions are favourable for the survival of juvenile forms and when adequate food is available, besides protection from predators. Monthly variations of GSI of Serra Spanish mackerel showed that peak breeding coincides with rainy season and possibly better environmental conditions.

It is interesting to observe that the peak breeding season of Serra Spanish mackerel in northeastern Brazil takes place in a sequential manner. In the coastal areas of Natal the spawning season is from March-June whereas in the Maranhão coastal waters of Brazil spawning occurs in October (Batista and Fabré, 2001), and from June to November (Lima, 2004). A similar trend was observed in Australia for Spanish mackerel S. commerson Lacepède (Mackie et al., 2005). These probably reflect their migratory route for feeding and reproductive purposes.

Conservation of fish stocks in their natural habitat are usually endangered by abusive fishing of immature fishes which have not yet completed their reproductive cycle, as recruitment via reproduction is the means by which the resource is renewed. The REVIZEE SCORE-NE Program has carried out various extensive surveys to determine the conservation status of the of the fish stocks in their natural habitats. This report emphasises the importance of Serra S. brasiliensis as an important fishery resource in northeastern Brazil, based on the surveys carried out in the northeastern continental shelf waters (Lessa, 2006). These reports indicate that the annual rate of exploration of the Serra stock is around 25% to 29% in the northeastern coastal region, which is close to its maximum sustainable exploratory limit. This stock shows a declining tendency of its population (Nóbrega, 2002).

The traditional fishing communities depend on small scale artisanal fishery, which reflects their way of making a living and sustains their lifestyle. Though it is important to preserve this traditional fishery, it is also vital to programme the sustainability and conservation of coastal fisheries resources. The predatory fishing technique of beach seine nets, in which small mesh sizes are used in order to catch marine shrimps, accounts for a large by-catch of small sized immature Serra Spanish mackerel. The artisanal fishery beach-seines are operated in the shallow coastal waters, which captures the immature individuals of the pelagic stock. Measures should be taken to regulate this fishery in order to conserve this valuable fishery resource by increasing the size of capture.

Acknowledgements — The authors wish to thank the National Council for Scientific and Technological Development of Brazil (CNPq) for the financial support awarded during the study period (J. T. A. Ximenes de Lima, Grant nº. 141651/2005-9) and for the Research grants awarded (S. Chellappa, Grant nº. 307497/2006-2, A. Araújo, Grant nº. 302012/2006-0 and N. T. Chellappa, Grant nº. 306274/2003-5). The authors thank the REVIZEE SCORE-NE Program for the valuable data made available to the public through the extensive fishery resource surveys carried out in the northeastern continental shelf waters.

Received April 6, 2009

Accepted May 26, 2009

Distributed XXX XX, XXXX (With 5 figures)

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Publication Dates

• Publication in this collection
  02 Apr 2010
• Date of issue
  May 2010

History

• Received
  06 Apr 2009
• Accepted
  26 Mar 2009