SciELO - Scientific Electronic Library Online

 
vol.52 issue3Screening for WSSV in crustacean from marine areas of Buenos Aires, Argentina author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

  • On index processCited by Google
  • Have no similar articlesSimilars in SciELO
  • On index processSimilars in Google

Share


Revista de biología marina y oceanografía

On-line version ISSN 0718-1957

Rev. biol. mar. oceanogr. vol.52 no.3 Valparaíso Dec. 2017

http://dx.doi.org/10.4067/S0718-19572017000300021 

 

NOTA CIENTÍFICA

 

A first experience of Patagonian sprat Sprattus fuegensis spawning in captivity: Adult acclimation, egg and larval measurements

Una primera experiencia de desove de sardina austral Sprattus fuegensis en cautiverio: Aclimatación de adultos, mediciones de huevos y larvas

 

Elson Leal1*, Carlos Muñoz1, Guillermo Moyano1, Claudio Bernal1 and Antonio Aranis1

1Instituto de Fomento Pesquero, Blanco 839, Valparaíso, Chile.*elson.leal@ifop.cl


ABSTRACT

Relevant traits of eggs and larvae of Patagonian sprat (Sprattus fuegensis), obtained from adult reproduction in captivity conditions, were studied. Temperature for adult acclimation and for incubation of eggs and larvae was not controlled; however it ranged with a mean of 13 ± 2 °C. Adult sprat maintained in cylindrical ponds of 2000-L spawned spontaneously at the first night after catch, probably due to catch stress. The eggs were spherical with a diameter ranging between 0.89 and 1.06 mm (mean 1.00 ± 0.05 mm, n= 54). The larvae hatched between the fourth and fifth day after spawning and their size varied between 2.83 and 4.11 mm long (mean 3.56 ± 0.34 mm, n= 39). The yolk sac reached a volume of between 0.11 and 0.22 mm3 (mean 0.18 ± 0.033 mm3, n= 32) and was exhausted by the third day post hatching (dph). Larval growth only occurred during the endogenous feeding period (efp) and survival did not exceed 6 dph, probably due to inappropriate conditions for feeding and growth.

Key words: Sprattus fuegensis, captivity, egg, larvae


INTRODUCTION

In the small pelagic fish dynamic, egg and larval survival is a key factor to annual individual recruitment for the population. Its variability is modulated by environmental (Houde 2010) and biological factors such as the broodstock condition, initial egg size, yolk sac absorption (first exogenous feeding), or larval growing rate (Chambers et al. 1989, Pepin 1991, Houde 1994, Castro et al. 2009, Teletchea & Fontaine 2010).

Patagonian sprat Sprattus fuegensis (Jenyns, 1842) is an important commercial and ecological species of small pelagic fish in the fjord ecosystem of southern Chile. This sprat appears to play an important trophodynamics role since it provides a base for upper levels in the food marine web (Landaeta et al. 2011).

Studies of S. fuegensis and its biological features have focused on adult specimens. Aranis et al. (2007) confirm the presence of S. fuegensis in the inner sea of Chiloé, Chile. In this area, Leal et al. (2011) described its reproduction, reporting higher reproductive activity in spring and female maturation with an average fork length of 13.5 cm. Cerna et al. (2013) studied growth and mortality of S. fuegensis larvae based on otolith age analysis. On egg and larval traits, De Ciechomski (1971) used plankton samples taken from the Argentinian coast to describe embryonic development in Patagonian sprat. Studies carried out in Chile have only considered the distribution and egg and larva size in the fjords of the southern Chilean region (41.5°-53°S) (Bustos et al. 2008, Landaeta et al. 2011, Contreras et al. 2014). Thus, little is known about the basic features of early developmental stages. The few available studies have been done using samples taken from natural environment. Therefore, data regarding certain relevant traits, remain unclear.

To date, published studies have neither dealt with the maintenance of this species in captivity nor have they dealt with egg and larval collection in this condition. Thus, the objective of these first experiments was to describe the procedure for catching and maintaining adult specimens as well as to present our findings on relevant traits of the first developmental stages of S. fuegensis. This study examined the egg size, endogenous feeding period (efp) and larvae growing rate, among others aspects, under laboratory conditions.

 

MATERIALS AND METHODS

Adult catches and acclimation

In two catch events (October 13 and 26, 2016), adult living specimens of Patagonian sprat were collected from the inner sea of Chiloé, (Fig. 1) using purse seine boats. Specimens were collected with a 25-L bucket and kept in two 250-L tanks with recirculating sea water during transport to the hatchery. Approximately 550 and 1,100 specimens from the first and second catch, respectively began the acclimation process in 2 cylindrical ponds (2000-L each), with a density of 225 and 550 ind m-3 for each case. In both experiments, the fish were kept in filtered sea water (37 µm), with open flow and no additional oxygen. This was monitored 3 times a day and ranged mostly between 8 and 12 mg l-1. Water temperature was not regulated, but it ranged between 11 and 15 °C depending on the time of day. From the third day on, adults were fed ad libitum with a diet of pellets (Golden Rc 5220, Biomar Chile S.A.). Daily mortality counts were done and the dead fish were removed from the ponds. Only in the second experiment, a circular current (vortex) was fixed inside the ponds to stimulate swimming in the specimens.

 

Figure 1. Approximate position of catch event (black dots)
of patagonian sprat, collected from the inner sea of Chiloé
Figura 1. Posición aproximada de los eventos de captura (círculos
negros) de sardina austral colectada en la zona del mar
interior de Chiloé

Experiment design for egg and larval rearing

After spawning, the eggs were collected immediately using a 200-µm sieve placed outside the spawning tanks and then incubated in an 80-L container with filtered sea water, open flow, and temperatures of 13 ± 2 °C. Living zooplankton food was not added to the setting which was enriched with microalgae (Chaetoceros, Isochrysis, Nannochloropsis) and a protein complex (Mcrovit Hi Protein) before the larvae completely absorbed the yolk sacs.

Among 12 and 15 eggs and larvae were measured daily in vivo and preserved in 90% ethanol and 5% formalin, respectively. Eggs, larvae, and yolk sacs were all photographed with a built-in camera of a stereo microscope (10X magnification). Measurements were done with Image-Pro Plus software version 5.1 (©Media Cybernetics, Inc.). Yolk sac volume (mm3) was calculated according to the equation of a spheroid (De Ciechomski 1971), 4/3 π (a*b2), where a is half the maximum yolk sac length and b is half the maximum width of the yolk sac. The daily larval growth rate was estimated through a linear model: length (mm)= a+b*age (days).

 

RESULTS AND DISCUSSION

During transport to the hatchery, adult mortality was low, less than 2%. Nevertheless, it was high during the first 5 days of acclimation, reaching 90% and 77% in the first and second experiments, respectively. Mortality stabilized after day 6. In experiment one, all the fish had died by day 18. In experiment two, mortality stopped on day 28 of acclimation, and some 210 fully acclimated specimens (19%) remained in the ponds by day 40, until they were sacrificed for other analyses. In both experiments, the first adult fish began to accept food after day 5, while all individuals in the ponds were eating around day 15.

The 2 experiments differed in terms of adult acclimation. Experiment 2 procedures were more successful. These included recirculating seawater (without additional oxygen), circular currents in the ponds, and an initial number of around 1,000 specimens (500 per ponds).

Reproduction occurred only the first night after the catch in both experiments close to 23:30 h. Specimens spawned spontaneously, probably due to the catch stress. Previous experiences with other species indicate that, given suitable reproductive conditions, the stress of being caught may trigger spontaneous spawning in adults within 24 h of capture (Cleary et al. 2002, Plaza & Cerna 2015). Because the catches occurred during the reproductive period peak for Patagonian sprat (Leal et al. 2011), it was expected that the specimens would have spawned spontaneously within the first day in captivity.

The Figure 2 shows Patagonian sprat eggs and larvae in different developmental stages. In experiment 2, high incidence of unviable eggs and malformed larvae was observed. Thus, results for egg and larval measurements were referred to only in experiment one.

 

Figure 2. Patagonian sprat eggs and larvae in different stages of
development. a) Newly fertilized egg (day 0); b) advanced
embryo shortly before hatching (day 4); c) larva with yolk sac,
3 dph (lateral view); d) larva with completely
absorbed yolk sac, 6 dph (dorsal view)
Figura 2. Huevos y larvas de sardina austral en diferentes estados de
desarrollo. a) Huevo recién fecundado (día 0), b) embrión avanzado
poco antes de la eclosión (día 4), c) larva con saco vitelino,
3 dpe (vista lateral), d) larva con saco vitelino completamente
reabsorbido, 6 dpe (vista dorsal)

Eggs were spherical, between 0.89 and 1.06 mm in diameter (mean 1.00 ± 0.05 mm, n= 54). Despite some overlap, eggs in this study were smaller than those reported for Patagonian sprat by Landaeta et al. (2011) (0.922-1.361 mm), which included samples taken from the natural environment. These authors reported larger eggs in the colder waters (9 °C average) of southern Chile (50°-53°S). Our results differ even more regarding the range (1.035-1.175 mm) reported by De Ciechomsky (1971) for S. fuegensis eggs captured off the coast of southern Argentina (50°43'S). Those eggs were also collected from colder waters (6°C average) than the temperature registered in our experiment (13 ± 2°C). Several reports have indicated this inverse relationship between egg size and water temperature for fish populations (Funamoto & Aoki 2002, Castro et al. 2009). For S. sprattus in the Baltic Sea, Nissling (2004) reported egg size ranging from 1.21 to 1.51 mm in different times during the spawning season in temperatures reaching from 3.9 to 6.3 °C. In addition to environmental factors (e.g., temperature), maternal effect is also known to determine egg and larva size and/or quality (Chambers & Laggett 1996, Castro et al. 2009, Mark et al. 2014). Accordingly, possible differences in the physiological condition of the broodstock between the two experiments could have influenced the low hatching percentage, malformed larvae, and high mortality in experiment two.

Larval hatching occurred between days 4 and 5 after spawning measuring between 2.83 and 4.11 mm long (mean 3.56 ± 0.34 mm, n= 39). These results fully correspond with Garrido et al. (2015) for Sardina pilchardus. The authors used laboratory studies to show that the larvae averaged 3.6 ± 0.34 mm on hatching, which occurred 72 h after spawning at constant temperature of 15 °C.

The efp or yolk sac absorption occurred during 3 days post-hatch (dph) (Fig. 3A). The yolk sac reached a volume of between 0.11 and 0.22 mm3 (mean 0.18 ± 0.033 mm3, n= 32). Larvae with the fully absorbed yolk sac measured 5.91 ± 0.47 mm long on average.

 

Figure 3. Patagonian sprat yolk sac absorption (A) and larval
growth (B), under laboratory conditions
Figura 3. Absorción del saco vitelino (A) y crecimiento de las
larvas (A) de sardina austral bajo condiciones de laboratorio

 

During the first 5 days, the larvae grew according to the linear model (Fig. 3B), following the equation (n= 66): Longitude (mm) = 3.85 + 0.42 × age (days) (R2= 0.64, P= < 0.001). Larvae of day 6 was not considered in the lineal model, since some of the measurements were made on dead larvae.

Previous reports on S. fuegensis larval growth rates are unknown. Nevertheless, reports about the S. sprattus phalericus in the Adriatic Sea (Dulcic 1998) estimated larvae growth rates between 0.40 and 0.42 mm·day-1 with an average temperature of 10.8 °C. Also, Valenzuela & Vargas (2003), using otolith analyses, estimated growth rates for S. sprattus larvae, which ranged from 0.36 to 0.40 mm·day-1 at temperatures ranging between 11 and 13.5 °C in the North Sea. For S. pilchardus under laboratory conditions, Garrido et al. (2015) indicated larval rate growth of 0.25 mm·day-1 but for a larger incubation period (75 dph). The same authors claimed that in the lack of optimal feeding conditions, larval growth of S. pilchardus only occurred during the efp and survival did not exceed 11 dph. In our experiment, larvae survived only 6 dph (3 days after efp) In this case, starvation effected growth and massive larval mortality occurred due to the fact that the water was enriched only with microalgae and a protein complex. Living food supply (zooplankton) has been described as an essential requirement for larval fish survival in laboratory studies by several authors (Garrido et al. 2012, Peck et al. 2013, Caldeira et al. 2014).

Although we obtained relevant egg and larval measurements, we failed to achieve satisfactory larval survival rates over time. Thus, future experiments will require a better acclimation setting through greater control of temperature, along with sterilization and trials with different living food types (zooplankton). This will allow improving the larva growth rate estimation, including the exogenous feeding times.

 

ACKNOWLEDGMENTS

Adult specimens were collected as part of two research projects carried out by the IFOP and funded by ASIPA 2016-2017. We thank Mr. Sergio Lillo for his logistic support and Mrs. Javier Legua and Mr. Felipe Sánchez who caught specimens for experiment two. We are also grateful to the IFOP staff working in the Hueihue hatchery (Chiloé, Chile).

 

LITERATURE CITED

Aranis A, R Meléndez, G Pequeño & F Cerna. 2007. Sprattus fuegensis en aguas interiores de Chiloé, Chile (Osteichthyes: Clupeiformes. Clupeidae). Gayana 71(1): 102-113.         [ Links ]

Bustos CA, MF Landaeta & F Balbontín. 2008. Efectos ambientales sobre la variabilidad espacial del ictioplancton de Chile austral durante noviembre de 2005. Revista Chilena de Historia Natural 81: 205-219.         [ Links ]

Caldeira C, A Santos, P Ré, M Peck, E Zais & S Garrido. 2014. Effect of prey concentration on the Ingestion rates of Sardine (Sardina pilchardus) larvae reared in laboratory conditions. Marine Ecology Progress Series 517: 217-228.         [ Links ]

Moreno. 2009. Egg trait variations in anchoveta Engraulis ringens: a maternal effect to changing environmental conditions in contrasting spawning habitats. Marine Ecology Progress Series 381: 237-248.

Cerna F, E Leal, A Lopez & G Plaza. 2013. Age, growth and natural mortality of the Patagonian sprat Sprattus fuegensis (Jenyns, 1842) in Chiloé inland sea, southern Chile. Latin American Journal of Aquatic Research 42(3): 580-587.         [ Links ]

Chambers R & W Leggett. 1996. Maternal influences on variation in egg sizes in temperate marine fishes. American Zoologist 36: 180-196.         [ Links ]

Chambers R, C Leggett & W Brown. 1989. Egg size, female effects, and the correlations between early life history traits of capelin, Mallotus villosus: an appraisal at the individual level. Fishery Bulletin 87: 515-523.         [ Links ]

Cleary J, S Battaglene & N Pankhurst. 2002. Capture and handling stress affects the endocrine and ovulatory response to exogenous hormone treatment in snapper, Pagrus auratus (Bloch & Schneider). Aquaculture Research 33: 829-838.         [ Links ]

Contreras T, L Castro, S Montecinos, H Gonzalez, S Soto, M Muñoz & S Palma. 2014. Environmental conditions, early life stages distributions and larval feeding of patagonian sprat Sprattus fuegensis and common sardine Strangomera bentincki in fjords and channels of the northern Chilean Patagonia. Progress in Oceanography 129: 136-148.         [ Links ]

De Ciechomski J. 1971. Estudio sobre los huevos y larvas de sardina fueguina Sprattus fuegensis, y de Maurolicus muelleri, hallados en aguas adyacentes al sector patagónico argentino. Physis 30: 557-567.         [ Links ]

Dulcic J. 1998. Larval growth of sprat, Sprattus sprattus phalericus, larvae in the northern Adriatic. Fisheries Research 36 (2-3): 117-126.         [ Links ]

Funamoto T & I Aoki. 2002. Reproductive ecology of Japanese anchovy off the Pacific coast of eastern Hounshu, Japan. Journal of Fish Biology 60: 154-169.         [ Links ]

Garrido S, E Saiz, J Peters, P Ré, P Alvarez, U Cotano, D Herrero, A Murguía & X Irigoien. 2012. Effect of food type and concentration on growth and fatty acid composition of early larvae of the anchovy (Engraulis encrasicolus) reared under laboratory conditions. Journal of Experimental Marine Biology and Ecology 434/435: 16-24.         [ Links ]

Garrido S, R Ben-Hamadou, A Santos, S Ferreira, M Teodósio, U Cotano, X Irigoien, M Peck, E Saiz & P Ré. 2015. Born small, die young: Intrinsic, size-selective mortality in marine larval fish. Nature. Scientific Reports 5: 17065. <doi: 10.1038/srep17065>         [ Links ].

Houde E. 1994. Differences between marine and freshwater fish larvae: implications for recruitment. ICES Journal of Marine Sciences 51: 91-97.         [ Links ]

Houde E. 2010. Recruitment variability. In: Jakobsen T, M Fogarty, B Megrey & E Moksness (eds). Fish reproductive biology. Implication for assessment and management, pp. 91-171. Wiley-Blackwell, Oxford/Iowa.         [ Links ]

Landaeta MF, CA Bustos, P Palacios, P Rojas & F Balbontín. 2011. Distribución del ictioplancton en la Patagonia austral de Chile: potenciales efectos del deshielo de Campos de Hielo Sur. Latin American Journal of Aquatic Research 39: 236-249.         [ Links ]

Leal E, TM Canales, A Aranis & M González. 2011. Actividad reproductiva y longitud de madurez de sardina austral Sprattus fuegensis, en el mar interior de Chiloé, Chile. Revista de Biología Marina y Oceanografía 46: 43-51. Full text via SciELO         [ Links ]

Mark A, D Johnson & S Sogard. 2014. BOFFFFs: on the importance of conserving old-growth age structure in fishery populations. ICES Journal of Marine Science 71: 2171-2185.         [ Links ]

Nissling A. 2004. Effects of temperature on egg and larval survival of cod (Gadus morhua) and sprat (Sprattus sprattus) in the Baltic Sea - implications for stock development. Hydrobiologia 514: 115-123.         [ Links ]

Peck M, P Reglero, M Takahashi & IA Catalán. 2013. Life cycle ecophysiology of small pelagic fish and climate driven changes in populations. Progress in Oceanography 116: 220-245.         [ Links ]

Pepin P. 1991. Effect of temperature and size on development, mortality, and survival rates of the pelagic early life history stages of marine fish. Canadian Journal of Fisheries and Aquatic Sciences 48: 503-518.         [ Links ]

Plaza G & F Cerna. 2015. Validation of daily microincrement deposition in otoliths of juvenile and adult Peruvian anchovy Engraulis ringens. Journal of Fish Biology 86: 203-216.         [ Links ]

Teletchea F & P Fontaine. 2010. Comparison of early life-stage strategies in temperate freshwater fish species: trade-offs are directed towards first feeding of larvae in spring and early summer. Journal of Fish Biology 77: 257-278.         [ Links ]

Valenzuela G & C Vargas. 2002. Comparative larval growth rate of Sprattus sprattus in relation to physical and biological oceanographic features in the North Sea. Archive of Fishery and Marine Research 49(3): 213-230.         [ Links ]

Received 26 July 2017 and accepted 5 December 2017
Associate Editor: Mauricio Landaeta D.

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