SciELO - Scientific Electronic Library Online

 
vol.67 issue3Influence of temperature on microsporidia infections in a natural population of Simulium pertinax Kollar, 1832 (Diptera; Simuliidae)Blood parasites, total plasma protein and packed cell volume of small wild mammals trapped in three mountain ranges of the Atlantic Forest in Southeastern Brazil author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

Share


Brazilian Journal of Biology

Print version ISSN 1519-6984On-line version ISSN 1678-4375

Braz. J. Biol. vol.67 no.3 São Carlos Aug. 2007

http://dx.doi.org/10.1590/S1519-69842007000300018 

BIOLOGY

 

Hatching rates of resting eggs of 'Cladocera' (Crustacea; Branchiopoda) at a tropical bay, Brazil

 

Taxas de eclosão de ovos de resistência de 'Cladocera' (Crustacea; Branchiopoda) em uma baía tropical, Brasil

 

 

Mugrabe, G*; Barros, S.; Marazzo, A.; Valentin, JL.

Laboratório de Zooplâncton, Departamento de Biologia Marinha, Instituto de Biologia, Universidade Federal do Rio de Janeiro – UFRJ, Ilha do Fundão, Cidade Universitária, CEP 21949-900, Rio de Janeiro, RJ, Brazil

 

 


ABSTRACT

The aim of this study was to determine the development time of embryos and to estimate the hatching rates of resting eggs of cladocerans found in the sediment of Guanabara Bay, Rio de Janeiro, Brazil, under experimental conditions. Eggs were sorted by species (Penilia avirostris – Sididae; Pleopis polyphemoides and Pseudevadne tergestina – Podonidae) and incubated at a temperature of 25 °C, salinity 35 and photoperiod 12 hours light/ 12 hours dark. Hatching rates were about 38% for Pseudevadne tergestina and 28% for Pleopis polyphemoides. Embryos of resting eggs of Penilia avirostris developed comparatively slowly (hatching after 86 days of incubation), with a hatching rate of only 5%. It was observed that development and hatching of resting eggs of marine cladocerans suggest that pulses of recruitment may exist, thus contributing to the rapid appearance and maintenance of planktonic populations of these crustaceans in Guanabara Bay.

Keywords: Cladocera, resting eggs, hatching, Guanabara Bay, Brazil.


RESUMO

O objetivo do presente estudo foi determinar o tempo de desenvolvimento de embriões e estimar as taxas de eclosão de ovos de resistência de cladóceros encontrados no sedimento da baía de Guanabara, Rio de Janeiro, Brasil, sob condições experimentais. Os ovos foram separados por espécie (Penilia avirostris – Sididae; Pleopis polyphemoides e Pseudevadne tergestina – Podonidae) e incubados a 25 °C, salinidade 35 e fotoperíodo 12 horas claro 12 horas escuro. As taxas de eclosão foram de aproximadamente 38% para Pseudevadne tergestina e de 28% para Pleopis -polyphemoides. Os embriões dos ovos de resistência de Penilia avirostris desenvolveram-se de forma relativamente lenta (eclodindo apenas 86 dias após o início da incubação), com uma taxa de eclosão de apenas 5%. Foi observado que o desenvolvimento e a eclosão dos ovos de resistência de cladóceros marinhos sugerem que podem ocorrer em pulsos, contribuindo assim para o rápido aparecimento e manutenção destes crustáceos na baía de Guanabara.

Palavras-chave: Cladocera, ovos de resistência, eclosão, baía de Guanabara, Brasil.


 

 

1. Introduction

Marine cladocerans are seasonally abundant microcrustaceans, widely distributed in estuarine and continental shelf waters and the open sea, where they comprise a significant portion of the mesozooplankton community. Some authors (e.g., Egloff et al., 1997; Onbé, 1999) have suggested that gamogenesis (or sexual reproduction) is initiated under unfavorable environmental conditions. Females produce eggs that give rise to male and female individuals. After copula and fertilization, the female produces, in general, a single, larger egg, with a resistant outer membrane and full of vitellus, which is called a resting egg. After releasing, the egg sinks towards the sea bottom until environmental conditions become favorable again. When the egg hatches, a female individual is born to restart parthenogenic reproduction. Normally, a sharp decrease of the planktonic population is observed, as well as increased production of resting eggs (Onbé, 1978a, 1985; Egloff et al., 1997).

The benthic phase of cladocerans, in which they remain in the environment as resting eggs, is considered critical for the perpetuation of the species in the plankton. These eggs can remain viable for several years on the sea bottom. Hatching success depends on many factors: for example, a rise in temperature is considered a key factor for egg hatching (Barros et al., 2002).

Resting eggs of cladocerans occur in the sediment of Guanabara Bay (Barros et al., 2000). The viability of these eggs has not yet been tested. In this tropical bay, located in Rio de Janeiro State, intense eutrophication from high inputs of organic matter (Paranhos et al., 1995) may have become a determinant factor in the development and hatching of these eggs.

We followed the development of embryos and estimated hatching rates of resting eggs of marine cladocerans in the sediment of Guanabara Bay in order to estimate whether these may serve as a recruitment resource for planktonic populations in this highly impacted tropical bay.

 

2. Material and Methods

Sediment samples were taken by means of an Ekman grab at a fixed 15 m depth station in Guanabara Bay, where muddy sediment predominates. In the laboratory, resting eggs were sorted from sediment samples, adapting the method proposed by Onbé (1978b) which consists of washing the samples through a 100 µm mesh. The residue remaining on the mesh was transferred to centrifuge tubes with a dense solution composed of 1 kg sucrose in 1 liter of water. Samples were centrifuged 3 times at 3500 rpm for 3 minutes. The supernatant was collected after each centrifugation, and then analyzed under stereoscopic microscopy to sort resting eggs. The eggs were identified following the descriptions by Onbé (1991).

The resting eggs belonged to the genera Penilia (Penilia avirostris Dana, 1852), Pleopis (Pleopis -polyphemoides Leuckart, 1859) and Pseudevadne (Pseudevadne tergestina (Claus, 1877)). Immediately after sorting, 20 eggs of P. avirostris, 72 P. polyphemoides and 8 P. -tergestina were placed separately in 25 ml flasks containing filtered water collected from the bay. The eggs were incubated under constant temperature (25 °C) and salinity (35) conditions, similar to the water of the bay at the collecting point. The water in the flasks was changed daily in order to maintain constant salinity. Dissolved oxygen was at a saturated level (5-6 ml.L-1) and photoperiod was 12 hours light 12 hours dark. Since the main objective of this first study was not to test the influence of water conditions, but just to observe the viability of the resting eggs in the Guanabara Bay and due to the small volume of the flasks, we did not measure other indicator parameters of water quality, such as ammonia. However, it is known (Paranhos, 2002) that this nutrient is lower (<5.0 µM) at the entrance o f the bay when salinity is high (35), due to the coastal water input under the influence of the tide. Eggs from each flask were transferred by pipette to a Petri dish, and observed in a stereoscopic microscope to follow the embryo development.

 

3. Results

Resting eggs of Podonidae are spherical, with a mean diameter of 200 µm, and may have ornamentation on the outer membrane (Pleopis), or be smooth (Pseudevadne). The first signs of embryonic development in resting eggs of P. polyphemoides occurred after 11 days of incubation. The vitelline content, which occupied the entire inner space of the egg, formed a concentrated mass, creating a space between the vitellus and the outer membrane (Figure 1a). One side of the vitelline mass curved inwards (Figure 1b). After about two days it was possible to see the whole formation of the embryo. The presence of red pigment in the eye corresponds to the final phase of embryonic development, when the egg is about to hatch. Before hatching, it was possible to observe that the egg was divided into two distinct parts. The outer membrane was then broken at the line site (Figure 1c), followed by a rupture of the inner membrane and hatching of the embryo (Figure 1d).

The development of resting eggs of P. tergestina is similar to P. polyphemoides. The only difference is the eye pigment, which is black (Figure 2b).

Resting eggs of P. avirostris are ovoid and flattened dorsal-ventrally, with a mean length of 250 µm and width of 192 µm (Figure 3). Their development follows a similar pattern to Pleopis polyphemoides. The black eye pigment appears only at the end of development.

 

 

3.1. Hatching rate and frequency

About 38% of the resting eggs of P. tergestina from Guanabara Bay hatched between day 20 and 31 after incubation, whereas for P. polyphemoides, hatching rates were about 28% (Figures 4 and 5). The embryonic development of such eggs was completed only 2 days after observation of the first signs of development.

 

 

 

 

Penilia avirostris had a single hatching egg (5%), after 86 days of incubation (Figure 5).

 

4. Discussion

Hatching synchronism may be a rule among marine cladocerans, as related by Madhupratap et al. (1996), who reported the same behavior. Observations of the embryonic developments of resting eggs made during this study agree with those of Onbé (1991), who observed that 50% of the eggs collected in the Inland Sea of Japan hatched in 15-17 days; while Madhupratap et al. (1996) observed a maximum hatching rate during days 20-30 at 15 °C.

Onbé (1991), on the other hand, observed hatching resting eggs at lower temperatures (20 °C) after about 4 days following the first noticeable signs of embryonic development. New experiments are necessary to explain these differences and elucidate the environmental factors which may influence embryonic development time and induce the hatching of resting eggs of Penilia avirostris in Guanabara Bay.

Various hypotheses could be suggested to explain the non-hatching of the majority of the resting eggs collected during this study. The unknown date of when the eggs were released into the water column is the main obstacle for such an attempt. We do not know if they became unviable because of a long time spent in the sea bottom, or if they have a longer period of latency, which can vary with environmental conditions. According to Onbé (1985), resting eggs can lose their viability because of environmental deterioration in the sediment, such as deoxygenation, as well as a production of ammonia, sulfide gas and other toxic substances. Onbé (1985) suggested that in polluted locations these eggs can be buried in deeper layers in the sediment, due to increased sedimentation rates, and this burial can eventually cause the death of the embryos because of the toxic conditions in the sediment.

This preliminary investigation allowed us to reach certain conclusions about the viability of cladoceran resting eggs in Guanabara Bay. Embryonic development phases and egg hatching follow the same pattern as other areas in the world. Resting eggs of P. -tergestina and P. polyphemoides from Guanabara Bay hatched earlier under incubation conditions and had a higher cumulative hatching success than the eggs of P. avirostris. A better understanding of the ideal conditions for the incubation and maintenance of P. avirostris, as well as the environmental factors favorable to its embryonic development is needed. The development and hatching synchronism of resting eggs of marine cladocerans suggest that pulses of recruitment may exist, thus contributing to the rapid appearance and maintenance of planktonic populations of these crustaceans in Guanabara Bay.

Acknowledgments — We would like to thank Francisco Matos for his help during field trips in Guanabara Bay and Yocie Yoneshigue-Valentin and Inácio Domingos for their contribution to this work. Financial support was provided by the Fundação de Amparo à Pesquisa no Estado do Rio de Janeiro, the Conselho Nacional de Desenvolvimento Científico e Tecnológico and the 'Programa de Apoio a Núcleos de Excelência'.

 

References

BARROS, S., ALECRIM, VP., MARAZZO A. and VALENTIN, JL., 2000. Resting eggs of cladocerans in the Guanabara Bay – RJ, Brazil: horizontal, vertical and temporal distribution. Nauplius, vol. 8, no 2, p. 237-244.        [ Links ]

BARROS, S., MARAZZO, A. and VALENTIN, JL, 2002. Comparing the efficiency of two sampling devices for collecting resting eggs of marine cladocerans. Nauplius, vol. 10, no. 1, p. 73-76.        [ Links ]

EGLOFF, DA., FOFONOFF, PW. and ONBÉ, T., 1997. Reproductive biology of marine cladocerans. In Advances in Marine Biology. Academic Press, vol. 31, p. 79-167.        [ Links ]

MADHUPRATAP, M., NEHRING, S. and LENZ, J., 1996. Resting eggs of zooplankton (Copepoda and Cladocera) from the Kiel Bay and adjacent waters (southwestern Baltic). Marine Biology, vol. 125, no 1, p. 77-87.        [ Links ]

ONBÉ, T., 1978a, The life cycle of the marine cladocerans. Bulletin of the Plankton Society of Japan, vol. 25, no 1, p. 41-54 (in Japanese with abstract in English).        [ Links ]

-, 1978b. Sugar flotation method for sorting the resting eggs of marine cladocerans and copepods from sea-bottom sediment. Bulletin of the Japanese Society of Scientific Fisheries, vol. 44, no 12, 1411p.        [ Links ]

-, 1985. Seasonal fluctuations in the abundance of populations of marine cladocerans and their resting eggs in the Inland Sea of Japan. Marine Biology, vol. 87, no 1, p. 83-88.        [ Links ]

-, 1991. Some aspects of the biology of resting eggs of marine cladocerans. In Crustacean Egg Production. Crustacean Issues 7. A. A. Balkema, Rotterdam, p. 41-55.        [ Links ]

-, 1999. Ctenopoda and Onychopoda (= Cladocera). In South Atlantic Zooplankton, Backhuys Publishers, Leiden, p. 797811.        [ Links ]

PARANHOS, R., NASCIMENTO, SM., and MAYR, LM., 1995. On the faecal pollution in Guanabara Bay, Brazil. Fresenius Environmental Bulletin: The International Journal for Rapid Communication and Updating in the Field of Biotic and Antibiotic Systems, vol. 4, no 6, p. 352-357.        [ Links ]

PARANHOS, R., 2002. Densidade e atividade de bactérias heterotróficas na Baia de Guanabara. Tese de Doutorado em Ciências, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, p. 116.        [ Links ]

 

 

Received July 20, 2005
Accepted March 23, 2006
Distributed August 31, 2007

 

 

* e-mail: glenda@biologia.ufrj.br

Creative Commons License All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License