Acessibilidade / Reportar erro

Oxygen consumption and ammonia excretion of the searobin Prionotus punctatus (Scorpaeniformes, Triglidae) at two different temperatures

Abstracts

Routine oxygen consumption and ammonia excretion were measured at 20ºC and 25ºC in the searobin Prionotus punctatus collected in Ubatuba region (22º30'S), SP, Brazil, in western South Atlantic, to investigate energy expenditure and losses through metabolic processes. IndividuaIs ranging from 1.00g to 88.47g and from 1.79g to 56.50g were used in experiments at 20ºC and 25ºC, respectively. At 20ºC and 25ºC, the averages of weight-specific oxygen consumption for the weight class of 1.00 - 10.00g, common to both temperatures, were 162.46µ 39.51 µ.10z/g/h and 200.47µ 92.46 µ.10z/g/h, respectively; for the weight class of 50.01 - 60.00g these values were 112.30 µ 22.84 µ.10z/g/h and 114.60 µ 20.36 µ.10zlg/h. At 20ºC and 25ºC, the averages of weight-specific ammonia excretion for the weight class of 1.00 to 1O.00g were 1.03 µ 0.37 fJ.M/g/h and 1.21 µ 0.65 µ.M/g/h, respectively; for the weight class of 50.01 -60.00g these values were 0.68 µ 0.13 fJ.M/g/h and 0.60 µ 0.22 µ.M/g/h. The energy budget for the species was calculated at both temperatures using the experimental data and a model for marine teleosts proposed in the literature.

Marine fish; Bioenergetics; Animal metabolism; Energy budget; Excretory products; Oxygen consumption; Prionotus punctatus; Ubatuba; São Paulo; Brazil


O consumo de oxigênio de rotina e a excreção de amônia de Prionotus punctatus coletados na região de Ubatuba (22º30'S), SP, Brasil, foram medidos a 20ºC e 25ºC, para avaliar os gastos e perdas de energia com os processos metabólicos. Foram utilizados indivíduos variando de 1,00g a 88,47g e de 1,79g a 56,50g, em experimentos a 20ºC e 25ºC, respectivamente. As médias de consumo específico de oxigênio a 20ºC e 25ºC para a classe de peso de 1,00 - 10,00g, comum a ambas as temperaturas, foram 162,46µ 39,51 µ.10z/g/h e 200,47 µ 92,46 µ.10z/g/h, respectivamente; para a classe de peso de 50,01 - 60,00g esses valores foram 112,30 µ 22,84 µ.10z/g/h e 114,60 µ 20,36 µ.10z/g/h. A 20ºC e 25ºC, as médias de excreção específica de amônia para a classe de peso de 1,00 a 10,00g foram 1,03 µ 0,37 e 1,21 µ 0,65 µ.M/g/h, respectivamente; para a classe de peso de 50,01 - 60,00g esses valores foram 0,68 µ 0,13 µ.M/g/h e 0,60 µ 0,22 µ.M/g/h. O orçamento energético para a espécie foi calculado para cada temperatura utilizando-se os da.dos experimentais e modelo proposto na literatura.

Peixes marinhos; Bioenergética; Metabolismo animal; Orçamento energético; Produtos de excreção; Consumo de oxigênio; Prionotus punctatus; Ubatuba; São Paulo; Brasil


RESEARCH ARTICLES

Oxygen consumption and ammonia excretion of the searobin Prionotus punctatus (Scorpaeniformes, Triglidae) at two different temperatures

Vicente Gomes; Phan Van Ngan; Maria José de Arruda Campos Rocha Passos; Liliana Lucia Christina Forneris

Instituto Oceanográfico da Universidade de São Paulo (Caixa Postal 66149, 05315-970 São Paulo, SP, Brasil)

ABSTRACT

Routine oxygen consumption and ammonia excretion were measured at 20ºC and 25ºC in the searobin Prionotus punctatus collected in Ubatuba region (22º30'S), SP, Brazil, in western South Atlantic, to investigate energy expenditure and losses through metabolic processes. IndividuaIs ranging from 1.00g to 88.47g and from 1.79g to 56.50g were used in experiments at 20ºC and 25ºC, respectively. At 20ºC and 25ºC, the averages of weight-specific oxygen consumption for the weight class of 1.00 - 10.00g, common to both temperatures, were 162.46µ 39.51 µ.10z/g/h and 200.47µ 92.46 µ.10z/g/h, respectively; for the weight class of 50.01 - 60.00g these values were 112.30 µ 22.84 µ.10z/g/h and 114.60 µ 20.36 µ.10zlg/h. At 20ºC and 25ºC, the averages of weight-specific ammonia excretion for the weight class of 1.00 to 1O.00g were 1.03 µ 0.37 fJ.M/g/h and 1.21 µ 0.65 µ.M/g/h, respectively; for the weight class of 50.01 -60.00g these values were 0.68 µ 0.13 fJ.M/g/h and 0.60 µ 0.22 µ.M/g/h. The energy budget for the species was calculated at both temperatures using the experimental data and a model for marine teleosts proposed in the literature.

Descriptors: Marine fish, Bioenergetics, Animal metabolism, Energy budget, Excretory products, Oxygen consumption, Prionotus punctatus, Ubatuba, São Paulo, Brazil.

RESUMO

O consumo de oxigênio de rotina e a excreção de amônia de Prionotus punctatus coletados na região de Ubatuba (22º30'S), SP, Brasil, foram medidos a 20ºC e 25ºC, para avaliar os gastos e perdas de energia com os processos metabólicos. Foram utilizados indivíduos variando de 1,00g a 88,47g e de 1,79g a 56,50g, em experimentos a 20ºC e 25ºC, respectivamente. As médias de consumo específico de oxigênio a 20ºC e 25ºC para a classe de peso de 1,00 - 10,00g, comum a ambas as temperaturas, foram 162,46µ 39,51 µ.10z/g/h e 200,47 µ 92,46 µ.10z/g/h, respectivamente; para a classe de peso de 50,01 - 60,00g esses valores foram 112,30 µ 22,84 µ.10z/g/h e 114,60 µ 20,36 µ.10z/g/h. A 20ºC e 25ºC, as médias de excreção específica de amônia para a classe de peso de 1,00 a 10,00g foram 1,03 µ 0,37 e 1,21 µ 0,65 µ.M/g/h, respectivamente; para a classe de peso de 50,01 - 60,00g esses valores foram 0,68 µ 0,13 µ.M/g/h e 0,60 µ 0,22 µ.M/g/h. O orçamento energético para a espécie foi calculado para cada temperatura utilizando-se os da.dos experimentais e modelo proposto na literatura.

Descritores: Peixes marinhos, Bioenergética, Metabolismo animal, Orçamento energético, Produtos de excreção, Consumo de oxigênio, Prionotus punctatus, Ubatuba, São Paulo, Brasil.

Full text available only in PDF format.

Texto completo disponível apenas em PDF.

Acknowledgements

We are grateful to the Oceanographie Institute of São Paulo University (IOUSP), to the Interministerial Commission of Brazilian Sea Resources (SECIRM) for financial support and to the Brazilian Researeh Couneil (CNPq) for the reaseareh and productivity grants (Procs 301480/91-0 RN and 300299/77-0 RN). We also thank the staff of our laboratory for their help throughout this project, as also the anonymous referees for their careful readings and valuable suggestions.

(Manuscript received 03 November 1998; revised 30 April1998; accepted 08 November 1999)

  • Aarset, A. V. & Aunaas,T. 1990. Metabolie responses of the sympagie amphipods Gammarus wilkitzkii and Onisimus glacialis to aeute temperature variations. Mar. Biol., 107(3):433-438.
  • Aristizabal Abud, E. O.; Prenski, L. B. & Daleo, G. R. 1992. Growth and energy budget in juvenile croaker (Micropogonias fumieri (Desmarest 1823)). ICES J. mar. Sei., 49(1):65-68.
  • Brandt, S. B. & Hartman, K. 1. 1993. Innovative approaehes with bioenergetie models: future applications to fish ecology and management. Trans. Amer. Fish. Soc., 122(5):731-735.
  • Brett, J. R. 1985. Correction in use of oxyealorifie equivalent. Cano J. Fish. aquat. Sei., 42(7): 13261327.
  • Brown, L. R. 1989. Temperature preferences and oxygen consumption of three species of seulpin (Cottus) ftom the Pit River drainage, California. Environ. Biol. Fishes, 26(3):223-236.
  • Castro Filho, B. M. de; Miranda, L. B. de & Miyao, S. Y. 1987. Condições hidrográficas na plataforma continental ao largo de Ubatuba: variações sazonais e em média escala. Bolm. Inst. oceanogr., S Paulo, 35(2):135-151.
  • Cockcroft, A C. & DuPreez, H. H 1989. Nitrogen and energy loss via nonfaecal and faecal excretion in the marine teleost Lithognathus lithognathus. Mar. Biol., 101(3):419-425.
  • Cockcroft, A C. & DuPreez, H. H 1990. Nitrogen and energy loss in the marine teleost Lithognathus mormyrus (Linnaeus). 1. expl mar. Biol. Ecol., 140(3):159-171.
  • DuPreez, H. H.; MeLaehlan, A & Marais, J. F. K. 1986. Oxygen consumption of a shallow water teleost, the spotted grunter, Pomadasys commersoni (Lacépéde, 1802). Comp. Biochem. Physiol.,84A(I):61-70.
  • DuPreez, H H; MeLaehlan, A; Marais, J. F. K. & Cockcroft, A C. 1990. Bioenergeties of fishes in a high-energy surf-zone. Mar. Biol., 106(1):1-12.
  • Elliot, J. M. & Davidson, W. 1975. Energy equivalents of oxygen consumption in animal energeties. Oecology, 19: 195-201.
  • Figueiredo, J. L. & Menezes, N. A 1980. Manual de peixes marinhos do sudeste do Brasil. III. Teleostei (2). São Paulo, MZ-USP. 9Op.
  • Fox, H. M. & Wingfield, C. A. 1938. A portable apparatus for the determination of oxygen dissolved in a small volume of water. 1. expl Biol., 15:437-445.
  • Gilman, L. S. 1994. Ao energy budget for northern sand lace, Ammodytes dubius, on Georges Bank, 1977-1986. Fish. Bull., 92(3):647-654.
  • Hoss, D. E. 1967. Rates of respiration of estuarine fish. In: ANNUAL CONFERENCE OF THE SOUTHERN ASSOCIA TION OF GAME AND FISH COMMISSIONERS, 21 si. New Orleans, 1967. Proceedings. New Orleans, SAGFC. p. 416-423.
  • Karas, P. & Thoresson, G. 1992. An application of a bioenergetic model to Eurasian perch (Perca fluviatilis L.). J. Fish. Biol., 41(2):217-230.
  • Kleiber, M. 1947. Body size and metabolic rate. Physiol. Rev., 27:511-541.
  • Koroleff, F. 1970. Direct determination of ammonia in natural waters as indophenol blue. Cons. Int. Explor. Mer, (3):122-124.
  • Lesser, M. P.; Martini, F. H. & Heiser, J. B. 1996. Ecology of the hagfish, Myxine glutinosa L. in the Gulf of Maine. I. Metabolic rates and energetics. J. expl mar. Biol. Ecol., 208(1/2):215-225.
  • MacIsaac, P. F.; Golf, G. P. & Speare, D. J. 1997. Comparison of routine oxygen consumption rates of three species of pleuronectids at three temperatures. J. Appl. Ichthyol., 13(4):171-176.
  • Marques, N. & Barreto, L. M. 1997. Cronobiologia: princípios e aplicações. São Paulo, EDUSP. 321p.
  • Meyer, J. L. & Schultz, E. T. 1985. Migrating haemulid fishes as a source of nutrients and organic matter on coral reefs. Limnol. Oceanogr., 30(1): 146-156.
  • Musatov, A. P. 1994. The van't-Hoff temperature coefficient of energy metabolism in lower vertebrates. Hydrobiol. J., 30(5):96-99.
  • Phan, V. N.; Gomes, V.; Carvalho, P. S.. M. & Passos, M. J. A. C. R. 1997. Effect of body size, temperature and starvation on oxygen consumption of Antarctic krill Euphaus;a superba. Rev. bras. oceanogr., 45(1/2):1-10
  • Phan, V. N.; Gomes, V.; Morais, D. M. & Passos, M. J. A. C. R. 1993. Estudo bioenergético de animais marinhos costeiros. I. Paralonchurus brasiliensis(Perciformes, Sciaenidae). PUblção esp. Inst. oceanogr., S Paulo, (10): 199-21.5.
  • Phan, V. N.; Gomes, V. & Passos, M. J. A. C. R. 1998. Routine metabolism and ammonia excretion of the Antarctic amphipod Bovallia gigantea (Pfetfer, 1988) (Crustacea, Amphipoda) in two. distinct temperatures. Pesq. antárt. bras., 3(1): 77-85.
  • Ricker, W. E. 1968. Methods for assessment of fish production in tTesh waters. London, IBP. 313p.
  • Rocha, G. R. A. & Rossi-Wongtschowski, C. L. D. B. 1998. Demersal fish community on the inner shelf of Ubatuba, southeastem Brazil. Rev. bras. oceanogr.,46(2):93-109.
  • Schmidt-Nielsen, K. . 1990. Animal physiology: adaptation and environment. 4th ed. Cambridgel New York, Cambridge University Press. 602p.
  • Soares, L. S. H. & Apelbaum, R. 1994. Atividade alimentar diária da cabrinha Prionotus punctatus (Teleostei, Triglidae) do' litoral de Ubatuba, Brasil. Bolm Inst. oceanogr., S Paulo, 42(1/2):85-98.
  • Soares, L. S. H.; Jarre- Teichmann, A. & Rossi-Wongtschowski, C. L. D. B. 1998. Field estimates of food consumption of the searobin Prionotus pünctatus (Bloch, 1797) on the continental shelf off Ubatuba, southeastem Brazil. Rev. bras. oceanogr., 46(1):45-60.
  • Opalinski, W. K. 1991. Respiratory metabolism and metabolic adaptations of Antarctic krill Euphausia superba. Pol. Archs Hydrobiol., 38(2): 183-263.
  • Paul, A. J. 1997. The use of bioenergetic measurements to estimate prey consumption, nutritional status and thermal habitat requirements for marine organisms reared in the sea. Buli. nato. Res. Inst. Aquuicult., Suppl. 3: 59-68.
  • Teixeira, R. L. & Haimovici, M. 1989. Distribuição, reprodução e hábitos alimentares de Prionotus punatatus e P. nudigula (Pisces: Triglidae) no litoral do Rio Grande do Sul. Atlântica, 11(1):13-45.
  • Thetmeyer, H. 1997. Diel rhythms of swimming activity and oxygen consumption in Gobiusculus Jlavescens (Fabricius) and Pomatoschistus minutus (Palias) (Teleostei: Gobiidae). J. expl mar. Biol. Ecol., 218(2): 187-198.
  • Winberg, G. G. 1956. Rate of metabolism and food requirements of fishes. (Transl. ftom Russian). Fish. Res. Bd Cano Transl. ser., (194):1-253.
  • Xie, X. J. & Sun, R. 1993. Pattem of energy allocation in the southern catfish (Silurus meridionalis). J. Fish. Biol., 42(2): 197-207.
  • Zar, J. H. 1984. Biostatistical analysis 2nd 00. EngleWood Cliffs, Prentice Hall. 718p.

Publication Dates

  • Publication in this collection
    22 Apr 2013
  • Date of issue
    1999

History

  • Reviewed
    30 Apr 1998
  • Received
    03 Nov 1998
  • Accepted
    08 Nov 1999
Instituto Oceanográfico da Universidade de São Paulo Praça do Oceanográfico, 191, 05508-120 São Paulo SP Brasil, Tel: (55 11) 3091-6513, Fax: (55 11) 3032-3092 - São Paulo - SP - Brazil
E-mail: amspires@usp.br