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Murray cod, Maccullochella peeli, spawned naturally in earthen ponds in four consecutive breeding seasons. Spawning was induced by a rise in water temperature up to or above 20°C during spring, however, an associated rise in water level was not required. Response to the temperature rise was more rapid later in the season and increasing daylength may have also been involved. Eggs were deposited on firm substrates at depths between 0·5 and 2·3 m, and hollow pipes, logs or similar structures were not necessary to provide suitable sites for egg deposition. At two spawning sites, mud had been removed from the pond banks by the broodfish and the eggs attached to the exposed clay. At one spawning site, a male cod was observed protecting the eggs during incubation. It is suggested that high survival of cod larvae will only occur when a significant rise in water level coincides with the breeding season and as a consequence the control of water levels for irrigation and flood mitigation purposes during spring and summer has affected Murray cod to a greater extent than golden perch, Macauaria ambigua, which spawns only after a substantial rise in water level, when conditions are more favourable for larval survival.

The eastern freshwater cod, Maccullochella ikei, from the Clarence River system, NSW, is described and M. peelii mariensis is described as a new subspecies from the Mary River system, Qld. The Murray cod, M. p. peelii and the trout cod, M. macquariensis, are indigenous to the Murray-Darling River system. Using electrophoretic data for 19 presumed loci, the coefficient of genetic identity between M. p. peelii and M. ikei was 0.72 and the banding-patterns of the muscle general protein, liver esterases and five other enzymes, were species-specific. A high proportion of abnormal and inviable hybrid larvae in a cross-breeding experiment indicate that post-zygotic isolating mechanisms have evolved between M. p. peelii and M. ikei. The coefficient of genetic identity between M. p. peelii and M. p. mariensis was 0.85 and banding patterns of muscle general protein were diagnostic. Canonical variates analysis using 18 morphological and nine meristic characters, clearly separated both spccies and the subspecies. Maccullochella ikei is distinguished from M. p. peelii by having longer pelvic fins, larger orbit length, and larger and morphologically distinct sagittalotoliths. Maccullochella p. mariensis differs from M. p. pee/ii by the combination of a deeper and shorter caudal peduncle, longer pelvic fins, larger sagittal otoliths and lesser extension of the first anal pterygiophore towards the first caudal vertebra, and from M. ikei by the combination of a deeper caudal peduncle, greater postorbital head length, smaller orbit, larger interorbital width, fewer scale rows below the lateral line, shorter fifth-sixth dorsal spine and lesser extension of the first anal pterygiophore. Although each species has distinctive colouration and mottling, there is some intra-specific variation. Maccullochella macquariensis is distinct from the other species by having a straight head profile, jaws of similar length, 14 precaudal vertebrae and distinctive colouration. There was a dramatic reduction in the distribution and abundance of cod in the eastern drainage during the early 1900s and cod were probably extinct in the Richmond and Brisbane River systems by the end of the 1930s. Maccullochella ikei and M. p. mariensis are each represented by one, small population. Possible causes of the decline, and the management strategies taken to conserve the endangered M. ikei are discussed.

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