TL;DR: The adults of the different species differ from each other in their dependence on water movement, their preference for open or cryptic sites such as crevices or caves for resting, their size and their methods of feeding.
Abstract: Five species of abalone occur along the southern Australian coastline; of these three species, Haliotis laevigata Donovan, Haliotis roei Gray, and Haliotis ruber Leach, are of commercial importance; the other two species are Haliotis cyclobates Peron and Haliotis scalaris Leach. The habitat, movement, feeding behaviour, food, and ecological relationships with predators were studied for each species at three study sites. Each species of abalone occupies a distinctive microhabitat. H. cyclobates lives in calm-water places associated with communities of the seagrass Posidonia australis and the razor shell Pinna dolobrata; H. laevigata lives on open rock adjacent to sand in moderate to rough water localities; H. ruber prefers caves in calm- to rough-water localities; H. roei occurs in narrow crevices in the upper sublittoral on rough-water coasts ; H. scalaris is an under-boulder or crevice-living species. All species are sedentary, but may make local movements in search of food. Several species may occur in a given habitat but there is little microhabitat overlap. The seasonal variation in food eaten by each species is described. All species show preference for red algae and reject most species of brown algae, subsisting predominantly on red algae and seagrasses according to the possibilities of the habitat. H. laevigata feeds mainly on algal drift and H. roei is substantially a grazing species. The other species feed on algal drift or graze opportunistically. Water movement is an important environmental factor affecting the feeding of those species which feed on algal drift. H. laevigata and H. ruber feed best in conditions of moderate water movement but poorly if the water is too calm or too rough. Water movement elicits a characteristic feeding response in these species. The predators of abalone include fish, crabs, molluscs, and starfish; their interaction with abalone is discussed. Crevices, caves, and cavities under boulders provide a refuge in space from predators for H. roei, H. ruber, and H. scalaris and juveniles of other species, which appear to be confined to these places, except for nocturnal feeding excursions, by the activity of their predators. The adults of the different species differ from each other in their dependence on water movement, their preference for open or cryptic sites such as crevices or caves for resting, their size and their methods of feeding. These differences between the species, taken together, ensure that there will be very little overlap between them in the sorts of places that they seek to live in or their behaviour in seeking food; in those cases where food-seeking behaviour is similar, interspecific competition would seem to be negligible because food is abundant. Predation would seem to have been more important than interspecific competition as the selective pressure that established and maintains these differences between the species.
TL;DR: It is shown that fertilization may be a limiting factor in some exploited populations when distances separating spawning individuals are too large and recruitment failures reported for South Australian populations of H. laevigata have occurred when densities fell below ca.0.3 animals·m-2.
Abstract: A combination of laboratory and field experiments with the commercial abalone species Haliotis laevigata showed that fertilization may be a limiting factor in some exploited populations when distan...
TL;DR: A recent outbreak of mortality in Australian abalone was associated with neurotropic lesions, which have not previously been described in this country.
Abstract: Objective To investigate an outbreak of sudden severe mortality in farmed abalone from coastal Victoria.
Results The outbreaks occurred almost simultaneously in three farms following abalone movements from the wild and between farms. The initial on farm investigation identified a number of features that when considered together were highly suggestive of an infectious aetiology. In many cases, dead abalone had no significant gross lesions. Others had swollen mouths and some had prolapse and eversion of the radula. Histologically, the lesions centred on the nerves innervating the labial apparatus, primarily the cerebral and buccal ganglia, cerebral commissure and peripheral nerve branches arising from these. Nervous tissue necrosis and haemocyte infiltration were the dominant lesions seen microscopically in affected nerves.
Conclusions A recent outbreak of mortality in Australian abalone was associated with neurotropic lesions, which have not previously been described in this country. The on farm and between farm pattern of spread of the outbreak, a history of abalone movements linking farms, clinical observation of moribund and dead abalone were all highly suggestive of a virulent infectious agent.
TL;DR: A difference in the settlement response of two temperate commercial abalone species, Haliotis rubra and H. laevigata, is demonstrated, which was reflected in subsequent growth and survival during the early days of post-larval life.
TL;DR: The sizes at sexual maturity, sex ratios and the annual reproductive cycles of five sympatric species of abalone were studied and a gonad index and a stage frequency method based on measurement of oocyte diameters were used to determine the occurrence of spawning in each species.
Abstract: The sizes at sexual maturity, sex ratios and the annual reproductive cycles of five sympatric species of abalone (Haliotis cyclobates Peron, Haliotis laevigata Donovan, Haliotis roei Gray, Haliotis ruber Leach and Haliotis scalaris Leach) were studied at several sites in South Australia. The two species of commercial importance H. laevigata and H. ruber become sexually mature at about 3 years of age and between 75 and 120 mm long, according to growth rate. The other species are sexually mature at smaller sizes. In H. roei and H. cyclobates sex ratios were equal, but in the other species one sex tended to predominate; males were more numerous in younger populations and females in older populations of H. laevigata and H. scalaris, whereas males were more numerous in older populations of H. ruber. Possible explanations are advanced for these disparities. A gonad index and a stage frequency method based on measurement of oocyte diameters were used to determine the occurrence of spawning in each species. H. cyclobates and H. laevigata spawn synchronously during spring and summer at West I. and Tipara Reef; H. ruber spawns during autumn and winter at Tipara Reef and during spring and autumn at West I. ; H. roei and H. scalaris spawn throughout the year. The importance of the supply and availability of food and changes in sea temperatures as factors which can seasonally restrict the spawning periodicity of abalone are discussed.