Abstract
Oxygen consumption and ATP content are reported for the planktonic marine copepod Pontella mediterranea during normal and diapause embryonic development. In subitaneous embryos that hatched without delay within 48 h, O2 uptake increased linearly after spawning to reach maximum levels about 25 h later. By contrast, ATP levels were initially very high but decreased rapidly within the next 5 h to reach stable values thereafter. In diapause embryos, O2 consumption followed the typical U-shaped curve described for insect diapause. An initial period of prediapause, which lasted for about 25 days, was characterized by elevated O2 uptake. This was followed by a period of diapause in which O2 consumption dropped to 25% of the values recorded during prediapause. This protracted period of dormancy, which lasted about 4 to 5 months, was followed by a period of high O2 consumption possibly due to the breaking of diapause and resumption in development. ATP content during the pre-diapause period showed a similar trend as in subitaneous embryos with high initial levels that decreased with time for the first 20 days and remained stable afterwards.
Similar content being viewed by others
Abbreviations
- E :
-
embryo
- EDTA :
-
ethylenediamine-tetraacetic acid
- PCA :
-
perchloric acid
- SW:
-
sea water
- TEM :
-
transmission electron microscopy
References
Bartolucci S, Lancieri M, Di Jeso F, De Vincentiis M (1973) On the regulation of O2 consumption in sea urchin embryos in the presence of actinomycin D. Acta Embryol Exp 1: 105–113
Braune HJ (1976) Effects of temperature on the rates of oxygen consumption during morphogenesis and diapause in the egg stage of Leptoptera dolobrata (Heteroptera, Miridae). Oecologia 25: 77–87
Brewer RH (1964) The phenology of Diaptomus stagnalis (Copepoda, Calanoida): The development and the hatching of the egg stage. Physiol Zool 37: 1–20
Burkholder JR (1934) A quantitative study of respiratory metabolism in single developing egg (Orthoptera). Physiol Zool 7: 247–270
Carpenter JF, Hand SC (1986) Arrestment of carbohydrate metabolism during anaerobic dormancy and aerobic acidosis in Artemia embryos: determination of pH-sensitive control points. J Comp Physiol B 156: 451–459
Clegg JS, Cavagnaro J (1975) Interrelationship between water and metabolism in Artemia cysts IV-ATP and cyst hydratation. J Cell Physiol 88: 153–166
Clegg JS, Conte FP (1980) A review of the cellular and developmental biology of Artemia. In: Persoone G et al (eds) The brine shrimp Artemia, vol 2. Physiology, biochemistry, molecular biology. Universa Press, Wetteren, Belgium, pp 11–54
Yanagisawa T (1975) Respiration and energy metabolism. In: Czihak G (ed) The sea urchin embryo — biochemistry and morphogenesis. Springer Berlin Heidelberg New York, pp 510–538
Dutrieu J (1960) Observations biochimiques et physiologiques sur le developement d'Artemia salina. Arch Zool Exp Gen 99: 1–134
Elgmork K, Nilssen JP (1978) Equivalence of copepod and insect diapause. Verh Int Verein Limnol 20: 2511–2517
Grice GD, Gibson VR (1981) Hatching of eggs of Pontella mediterranea Claus (Copepoda, Calanoida). Vie et Milieu 31: 49–51
Grice GD, Marcus NH (1981) Dormant eggs of marine copepods.. Oceanogr Mar Biol Ann Rev 19: 125–140
Hofmann GE, Hand SC (1990) Subcellular differentiation arrested in Artemia embryos under anoxia: evidence supporting a regulatory role for intracellular pH. J Exp Zool 253: 287–302
Hofmann GE, Hand SC (1994) Global arrest of translation during invertebrate quiescence. PNAS 91: 8492–8496
Ianora A, Santella L (1991) Diapause embryos in the neustonic copepod Anomalocera patersoni. Mar Biol 108: 387–394
Mansingh A (1971) Physiological classification of dormancies in insects. Can Ent 103: 983–1009
Marcus NH (1979) On the population biology and the nature of diapause of Labidocera aestiva (Copepoda, Calanoida). Biol Bull 157: 297–305
Marcus NH (1980) Photoperiodic control of diapause in the marine calanoid copepod Labidocera aestiva. Biol Bull 159: 311–318
Marcus NH (1982a) The reversibility of simultaneous and diapause egg production by individual females of Labidocera aestiva (Copepoda, Calanoida). Biol Bull 162: 39–44
Marcus NH (1982b) Photoperiodic and temperature regulation of diapause in Labidocera aestiva. Biol Bull 162: 45–52
Marcus NH (1984) Variation in the diapause response of Labidocera aestiva (Copepoda, Calanoida) from different latitudes and its importance in the evolutionary process. Biol Bull 166: 127–139
Marcus NH (1986) Population dynamics of marine copepods: the importance of photoperiodism. Am Zool 26: 469–477
Marcus NH, Lutz R, Burnett W, Cable P (1994) Age, viability and vertical distribution of zooplankton resting eggs from an anoxic basin: evidence of an egg bank. Limnol Oceanogr 39: 154–158
Monroy A (1965a) Chemistry and physiology of fertilization. New York Holt, Renehart and Wiston
Monroy A (1965b) Biochemical aspects of fertilization. In: Weber R (ed) Descriptive biochemistry of animal development, vol. 1, New York, London, pp 73–135
Muramatsu S (1960) Studies on the physiology of Artemia embryos I. Respiration and its main substrates during early development of the encysted embryo. Embryologia 5: 95–106
Okada M (1971) Role of the chorion as a barrier to oxygen in the diapause silkworm, Bombyx mori L. Experientia 27: 658–660
Paterson GP (1977) A simplification of the protein assay method of Lowry et al. which is more generally applicable. Anal Biochem 83: 346–356
Perona R, Vallejo CG (1989) Mechanism of yolk degradation in Artemia: a morphological study. Comp Biochem Physiol 94A: 231–242
Rakshpal R (1962a) Respiratory metabolism during embryogenesis of Gryllus veletis (Alexander and Bigelow) (Orthoptera: Gryllidae). Physiol Zool: 47–51
Rakshpal R (1962b) Respiratory metabolism during embryogenesis of a diapause species of field cricket, Gryllus pennsylvanicus Burmeister (Ortoptera, Gryllidae). J Insect Physiol 8: 217–221
Rakshpal R (1962c) Diapause in the eggs of Gryllus pennsylvanicus Burmeister (Orthoptera: Gryllidae). Can J Zool 40: 179–194
Roemhild G (1965) Respiration of the eggs and part of eggs of Aulocara elliotti. Physiol Zool 38: 213–218
Santella L, Ianora A (1990) Subitaneous and diapause eggs in Mediterranean populations of Pontella mediterranea (Copepoda, Calanoida). Mar Biol 105: 83–90
Santella L, Ianora A (1992) Fertilization envelope in diapause eggs of Pontella mediterranea. Mol Repr Dev 33: 463–469
Strehler BL (1965) Adenosine-5′-triphosphate and creatine phosphate determination with luciferase. In: Bergmeyer HV (ed) Methods of enzymatic analysis. Academic Press, New York, pp 559–572
Tauber CA, Tauber JM (1981) Insect seasonal cycle: genetics and evolution. Annu Rev Ecol Syst 12: 281–308
Van der Linden A, Blust R, Van Laere AJ, Decleir W (1988) Light-induced release of Artemia dried embryos from diapause: analysis of metabolic status. J Exp Zool 247: 131–138
Watson NHF, Smallman BN (1971) The physiology of diapause in Diacyclops navus Herrick (Crustacea, Copepoda). Can J Zool 49: 1449–1454
Zoppini AM (1990) Adenosintrifosfato cellulare (ATP). Nova Thalassia 11: 225–230
Author information
Authors and Affiliations
Additional information
Communicated by H. Langer
Rights and permissions
About this article
Cite this article
Romano, G., Ianora, A., Santella, L. et al. Respiratory metabolism during embryonic subitaneous and diapause development in Pontella mediterranea (Crustacea, Copepoda). J Comp Physiol B 166, 157–163 (1996). https://doi.org/10.1007/BF00263978
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF00263978