Summary
Red and white muscle in the two Antarctic notothenioid fishes Dissostichus mawsoni and Pagothenia borchgrevinki show a rate of postmortem fall of 0.2 pH units per hour, which is close to the rate reported for mammalian muscle at 30°C, but the plateau value is reached several hours earlier in the Antarctic fish, indicating significantly lower stores of initial glycogen. A few particles, most likely representing glycogen, were seen in P. borchgrevinki white muscle and D. mawsoni red muscle, whereas predictably fewer glycogen still was evident in D. mawsoni white muscle. When large numbers of mitochondria and lipid stores were encountered in combination with a small amount of glycogen, we concluded that aerobic metabolism is dominant and that the two species examined would not use white trunk muscle for sustained or slow swimming. Rapid contractions of white trunk muscle as in prey capture or predator evasion are more likely.
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References
Black EC, Robertson CA, Lam KC, Chu WG (1962) Changes in glycogen, pyruvate and lactate in the rainbow trout (Salmo gairdneri) during and following muscular activity. J Fish Res Board Can 19:409–436
Chrystall BB, Devine CE (1978) Electrical stimulation, muscle tension and glycolysis in bovine sternomandibularis. Meat Sci 2:49–58
Davison W (1983) The lateral musculature of the common bully, Gobiomorphus cotidianus, a freshwater fish from New Zealand. J Fish Biol 23:143–151
Davison W, Macdonald JA (1985) A histochemical study of the swimming musculature of Antarctic fish. NZ J Zool (in press)
Devine CE, Ellery S, Averill S (1984) Responses of different types of ox muscle to electrical stimulation. Meat Sci 10:35–51
De Vries AL, Eastman JR (1981) Physiology and ecology of the notothenioid fishes of the Ross Sea. J R Soc NZ 11:329–340
De Witt HH (1971) Coastal and deepwater benthic fishes of the Antarctic In: Bushnell VC (ed) Antarctic map folio, vol 15. American Geographical Society, New York, pp 1–10
Eastman JT, De Vries AL (1982) Buoyancy studies of notothenioid fishes in McMurdo Sound, Antarctica. Copeia 1982:385–393
Eastman JT, De Vries AL (1985) Adaptations for cryopelagic life in the antarctic notothenioid fish Pagothenia borchgrevinki. Polar Biol 4:45–52
Franzini-Armstrong C, Porter KR (1964) Sarcolemnal invaginations constituting the T-system in fish muscle fibres. J Cell Biol 22:675–696
Hulbert WC, Guppy M, Murphy B (1979) Metabolic sources of heat and power in tuna muscles. 1. Muscle fine structure. J Exp Biol 82:289–301
Johnston IA, Harrison P (1985) Contractile and metabolic characteristics of muscle fibres from Antartic fish. J Exp Biol 116:223–236
Kalarski W, Smialowska E, Freidhuber A (1982) Histological analysis of fibres in myotomes of Antarctic fish. 2. Morphometry of muscle fibres and capillaries. Z Mikrosk-Anat Forsch 96:791–801
Lin Y, Dobbs GH, De Vries AL (1974) Oxygen consumption and lipid content in red and white muscles of antarctic fishes. J Exp Zool 189:379–385
Littlepage JL (1965) Oceanographic investigations in McMurdo Sound, Antarctica. In: Lliano GA (ed) Biology of the Antarctic seas vol II. Antarct Res, Ser 5. American Geophysical Union, Washington pp 1–37
Macdonald JA (1981) Temperature compensation in the peripheral nervous system: antarctic vs temperate poikilotherms. J Comp Physiol 142:411–418
Macdonald JA (1983) Neuromuscular cold adaptation in an antarctic fish. NZ Antarct Rec 5:1–10
Meyer-Rochow VB, Klyne MA (1982) Retinal organization of the eyes of three, notothenioid fishes from the Ross Sea (Antarctica). Gegenbaurs Morph Jahrb 128:762–777
Meyer-Rochow VB, Pyle CA (1980) Fatty acid analysis of lens and retina of two antarctic fish and of the head and body of the antarctic amphipod Orchomene plebs. Comp Biochem Physiol B 65:395–398
Murphy JA, Weberg A (1979) Routine use for various types of tissues of osmium ferrocyanide fixative after initial aldehyde fixation without need of further poststaining: comparison of its use with Epon, Epon replacements Poly/bed 812 and LX 112, Epon-Araldite, Spurr and ultralow viscosity resins. In: Bailey GN (ed) Proc 37th Elect Microsc Soc Claitor's Publishing Di, Baton Rouge, pp 344–345
Nag AC (1972) Ultrastructure and adenosine triphosphatase activity of red and white muscle fibres of the caudal region of a fish Salmo gairdneri. J Cell Biol 55:42–57
Smith MAK, Haschemeyer AEV (1980) Protein metabolism and cold adaptation in antarctic fishes. Physiol Zool 53:373–382
Walesby NJ, Johnston IA (1980) Fibre types in the locomotory muscles of an antarctic teleost Notothenia rossii. Cell Tissue Res 208: 143–164
Walesby NJ, Nicol CJM, Johnston IA (1982) Metabolic differentiation of muscle fibres from a haemoglobinless (Champsocephalus gunnari Lonnberg) and a red blooded (Notothenia rossii Fisher) antarctic fish. Br Antarct Surv Bull 51:201–214
Wells RMG, Tetens V, De Vries AL (1984) Recovery from stress following capture and anaesthesia of antarctic fish: haemotology and blood chemistry. J Fish Biol 25:567–576
Willemse JJ, Markus-Silvis L (1984) Prevention of fixation artefacts in microscopical investigations on muscle growth in cultured eels, Anguilla anguilla (L). Aquaculture 37:369–376
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Meyer-Rochow, V.B., Devine, C.E. Ultrastructural observations and pH-measurements on red and white muscle from Antarctic fish. Polar Biol 6, 241–246 (1986). https://doi.org/10.1007/BF00443402
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DOI: https://doi.org/10.1007/BF00443402