Generating age estimates for long-lived fish requires particular attention to validation because they are usually difficult to age owing to narrow increment structure. A robust validation of the accuracy and precision of banded morwong, Cheilodactylus spectabilis, sampled from Tasmanian waters, was undertaken. Age at the first enumerated increment was established from analysis of juvenile cohorts, and the timing and periodicity of increment formation was established using a quantitative model from oxytetracycline (OTC) mark-recaptures at liberty for periods of up to 8 years. The accuracy of age estimates was examined independently by comparing radiocarbon values in the otolith region corresponding to the first year of growth against the south-western Pacific calibration curve. C. spectabilis is very long-lived, with males and females living to over 90 years of age. Growth modelling revealed a fast initial growth phase, terminating in an abrupt plateau near the asymptotic length. This species displays substantial sexual dimorphism in growth, with males growing to larger sizes than females.

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The age of Notolabrus fucicola from the east and southeast coasts of Tasmania was estimated from counts of opaque (transmitted light) growth zones in thin transverse sections of sagittal otoliths. The position of the first annulus was validated through the otolith radii of known-age juveniles. Marginal increment analysis was performed by examining the growing edge of otoliths over 2 years. This showed that opaque zones were formed annually and were consistently deposited from late September to early December (spring season), which is coincident with annual increases in somatic growth and water temperature during this season. A criterion was developed to ensure accurate age estimation for individuals sampled during the time of year when deposition of opaque material was incomplete or not apparent. The maximum age estimated was 20 years and the relationship between fork length and age was described by the von Bertalanffy growth function (L∞ = 368 mm, K = 0.116 and t0 = –1.87 for males and L∞ = 385.7 mm, K = 0.109 and t0 = –1.96 for females). The clarity of increment structure and rigorous validation protocol that was adopted minimised the risks associated with using marginal increment analysis to validate the periodicity of increment formation and it provided robust age and growth estimates for N. fucicola in Tasmanian waters.

Banded morwong, Cheilodactylus spectabilis, a long-lived sedentary temperate reef fish, has undergone rapid changes in its growth and maturity characteristics along the east coast of Tasmania, Australia. Over a period of 10 years, growth of young males and females has consistently accelerated, such that in 2005, 3-year-old fish were up to 40 mm or 13% longer compared with 1996, and age at 50% maturity for females had declined from 4 to 3 years. The magnitude and speed of the observed changes were unexpected given the species’ longevity (maximum age of over 95 years). The underlying mechanisms for the changes remain unclear but density-dependent responses to changes in population size and age composition, possibly mediated through reduced competition for shelter and intra-specific interactions, may have been contributing factors. Increasing sea surface temperatures over part of the period of change does not appear to have been a major driver and a genetic response to fishing seems unlikely. Notwithstanding any uncertainty, C. spectabilis populations have become more productive in recent years, challenging the general approach towards stock assessment where life-history characteristics are assumed to remain stable across contrasting levels of stock abundance and environmental conditions.

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