Academic literature on the topic 'Sepia apama'

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Journal articles on the topic "Sepia apama"

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Sangster, C. R., and R. M. Smolowitz. "Description of Vibrio alginolyticus Infection in Cultured Sepia officinalis, Sepia apama, and Sepia pharaonis." Biological Bulletin 205, no. 2 (October 2003): 233–34. http://dx.doi.org/10.2307/1543270.

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Prowse, Thomas A. A., Bronwyn M. Gillanders, Barry W. Brook, Anthony J. Fowler, Karina C. Hall, Michael A. Steer, Camille Mellin, et al. "Evidence for a broad-scale decline in giant Australian cuttlefish (Sepia apama) abundance from non-targeted survey data." Marine and Freshwater Research 66, no. 8 (2015): 692. http://dx.doi.org/10.1071/mf14081.

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Little is known about the population trajectory and dynamics of many marine invertebrates because of a lack of robust observational data. The giant Australian cuttlefish (Sepia apama) is IUCN-listed as Near Threatened because the largest known breeding aggregation of this species in northern Spencer Gulf, South Australia, has declined markedly since the turn of the century. We used by-catch records from long-term trawl surveys to derive abundance data for S. apama and commercial cuttlefish harvest data as a measure of exploitation. Using Bayesian hierarchical models to account for zero-inflation and spatial dependence in these abundance counts, we demonstrated a high probability of broad-scale declines in the density of S. apama, particularly surrounding the primary aggregation site, which supports the recent closure of the entire S. apama fishery in northern Spencer Gulf. Historical harvest data were positively correlated with S. apama density estimated from the trawl surveys, suggesting that the commercial cuttlefish catch tracks the species abundance. Our results also indicated the possibility that the known S. apama breeding grounds might be supplemented by individuals that were spawned elsewhere in northern Spencer Gulf.
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Payne, Nicholas L., Edward P. Snelling, Jayson M. Semmens, and Bronwyn M. Gillanders. "Mechanisms of Population Structuring in Giant Australian Cuttlefish Sepia apama." PLoS ONE 8, no. 3 (March 11, 2013): e58694. http://dx.doi.org/10.1371/journal.pone.0058694.

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Cronin, E. R., and R. S. Seymour. "Respiration of the eggs of the giant cuttlefish Sepia apama." Marine Biology 136, no. 5 (June 16, 2000): 863–70. http://dx.doi.org/10.1007/s002270000274.

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Grist, Eric P. M., and George D. Jackson. "Energy balance as a determinant of two-phase growth in cephalopods." Marine and Freshwater Research 55, no. 4 (2004): 395. http://dx.doi.org/10.1071/mf03154.

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Many cephalopods exhibit early exponential growth, which abruptly shifts to a much slower rate. Using a simple model of the energy balance between intake from food and expenditure in growth plus metabolism, we consider how the two-phase growth pattern may be explained in terms of energy conservation. We determine the post-hatch size and age at which exponential growth would be expected to terminate. The model is tested with laboratory hatchling data obtained for the giant Australian cuttlefish Sepia apama. Together with growth data obtained for a related species, Sepia officinalis, model projections for critical transition size and age interestingly suggest that the metabolism of S. apama in the natural habitat may be three to four times higher than in captivity. A sensitivity analysis indicates that the critical transition size is in general more sensitive than critical transition time to any invoked changes in metabolic rate.
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Smith, H. C., and K. R. Sprogis. "Seasonal feeding on giant cuttlefish (Sepia apama) by Indo-Pacific bottlenose dolphins (Tursiops aduncus) in south-western Australia." Australian Journal of Zoology 64, no. 1 (2016): 8. http://dx.doi.org/10.1071/zo15075.

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We report on observations of Indo-Pacific bottlenose dolphins (Tursiops aduncus) feeding on giant cuttlefish (Sepia apama) from March 2007 to April 2013 in the temperate waters off Bunbury, south-western Australia. Seventeen feeding events were observed during the cooler months between July and September in relatively shallow coastal waters, with 12 dolphins identified as adult females. We observed behavioural sequences of complex prey-handling of cuttlefish where dolphins’ used multiple steps to remove the cuttlefish head, ink and cuttlebone before consuming the flesh of the cuttlefish mantle. Our study provides valuable information to the limited knowledge on the complex prey-handling by T. aduncus on cuttlefish in Australia, and is complementary to other known specialised foraging behaviours of bottlenose dolphins. This study also details a different behavioural sequence of cuttlefish prey-handling to that of the bottlenose dolphins in the Sado estuary, Portugal, where only the head is consumed, and to the Spencer Gulf, Australia, in that the dolphins in Bunbury carry the cuttlefish mantle over their rostrum before removing the cuttlebone. Information on S. apama in Bunbury is scarce, therefore studies on abundance, distribution and egg-laying sites are recommended in order to enable informed decision making and to understand the importance of S. apama to the diet of T. aduncus.
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Naud, Marie-José, and Jonathan N. Havenhand. "Sperm motility and longevity in the giant cuttlefish, Sepia apama (Mollusca: Cephalopoda)." Marine Biology 148, no. 3 (September 28, 2005): 559–66. http://dx.doi.org/10.1007/s00227-005-0109-z.

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Payne, Nicholas L., Bronwyn M. Gillanders, Roger S. Seymour, Dale M. Webber, Edward P. Snelling, and Jayson M. Semmens. "Accelerometry estimates field metabolic rate in giant Australian cuttlefish Sepia apama during breeding." Journal of Animal Ecology 80, no. 2 (September 28, 2010): 422–30. http://dx.doi.org/10.1111/j.1365-2656.2010.01758.x.

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Aitken, J. P., and R. K. O'Dor. "Respirometry and swimming dynamics of the giant australian cuttlefish,sepia apama(mollusca, cephalopoda)." Marine and Freshwater Behaviour and Physiology 37, no. 4 (December 2004): 217–34. http://dx.doi.org/10.1080/10236240400016579.

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Naud, Marie-José, Paul W. Shaw, Roger T. Hanlon, and Jon N. Havenhand. "Evidence for biased use of sperm sources in wild female giant cuttlefish ( Sepia apama )." Proceedings of the Royal Society B: Biological Sciences 272, no. 1567 (May 22, 2005): 1047–51. http://dx.doi.org/10.1098/rspb.2004.3031.

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Dissertations / Theses on the topic "Sepia apama"

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Cronin, Emma R. "Morphology, respiration and energetics of the eggs of the giant cuttlefish, Sepia apama /." Title page, contents and abstract only, 2000. http://web4.library.adelaide.edu.au/theses/09PH/09phc947.pdf.

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Hall, Karina Christine. "Life history and fishery of a spawning aggregation of the giant Australian cuttlefish Sepia apama." Thesis, 2003. http://hdl.handle.net/2440/65471.

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Every austral winter, thousands of giant Australian cuttlefish, Sepia apama Gray, 1849, aggregate to spawn over a small area of subtidal rocky reef in northern Spencer Gulf, South Australia, constituting the only known spawning aggregation of cuttlefish in the world. Rapid expansion of commercial fishing operations on the aggregation between 1994 and 1997 caused considerable concern for the sustainability of the population. However, determining an appropriate management strategy for the fishery was hampered by a paucity of biological information. Despite its large size and common occurrence, S. apama had previously attracted little scientific interest. Therefore, the general aim of this study was to provide some understanding of the life history of S. apama in the wider northern Spencer Gulf region and to relate this to the popUlation dynamics at the aggregation area. The dynamics of the spawning population were investigated using underwater visual transect methods from 1998 to 2001. Different time and area closures were implemented over this four-year period, allowing for comparisons between fished and unfished sites. Temporal trends in density indicated a distinct annual spawning season between May and August, with a consistent peak in early June. During the season densities as high as 85 cuttlefish.1OOm'2 were recorded, whereas at other times they were less than I cuttlefish.lOOm'2. Tagging work verified that individual cuttlefish remained at the aggregation area for a large part of the spawning season, such that it was valid to estimate total abundance and biomass at the time of peak numbers. In non-fished years total abundances reached over 170,000 individuals. Although biomass estimates indicated a decline in the total population size from 222 t in 1999 to 184 t in 2001, no long-term effects due to previous fishing could be concluded. Cuttlefish were not evenly distributed amongst habitats or sites within the aggregation area, although the pattern of distribution was consistent between years. To this effect, the original closed area in 1998 represented 43% of the estimated hard substrate but only accounted for 19 to 28% of the total estimated biomass in each year. Therefore, the spatial distribution and movement patterns of cuttlefish within the aggregation area have important implications for the implementation of future area closures. At non-spawning times, cuttlefish were widely distributed throughout the northern Spencer Gulf at much lower densities than those recorded at the aggregation area. One cuttlefish tagged 65 km south of the aggregation area was later recaptured at the spawning site, suggesting that the aggregated population is drawn from that of the broader region. There were multiple size classes within both the spawning and non-spawning populations of the Gulf, which suggested the presence of multiple year classes. The cuttlebones and other hard structures were examined as potential indicators of age. The width of growth increments in the cuttlebones varied seasonally over the length of the bone. The analysis of many bones indicated the existence of two year classes for each sex. They also suggested there were two alternative life cycle types in northern Spencer Gulf. The first was characterised by rapidly growing juveniles that attained maturity within 7 to 8 months, and which then returned to spawn as small adults in the first spawning season following hatching. The second life cycle type was characterised by slower growing juveniles that ultimately did not return to the aggregation area until the second year after hatching, and thus lived for nearly two years. Individuals conforming to the first life cycle type vastly outnumbered those of the second. Aquarium experiments using juveniles hatched and reared in captivity under different temperature and feeding regimes supported the above interpretation of the adult cuttlebone microstructures. Juveniles fed double rations achieved higher growth rates and had wider and more numerous growth increments in their bones than those fed half rations. The effect of temperature was confounded by the use of equal rations across temperature treatments rather than ad libitum feeding. Reproductive indices confirmed that all individuals at the aggregation area, irrespective of size or age, were mature and spawning, whilst those in the wider Gulf population were immature and feeding. Gonad weight and gamete size were positively correlated with body size in both sexes; suggesting a difference in the reproductive potential of the two different year classes. There was a decline in condition during spawning, supporting the hypothesis of a semel parous spawning strategy. The sex composition of the spawning population was highly biased toward males, with 3 to 6 males per female, whilst the sex ratio of the northern Spencer Gulf population tended toward unity. No single explanation for this disparity could be determined. The mating system was described through analysis of the reproductive behaviours of spawning individuals from video recordings. Many behaviours related to sexual selection were displayed by individuals of both sexes, which were consistent with expectations that relate to the biased operational sex ratio. Large and small males, representing the different year classes, used different behavioural tactics to compete for females, but there was no assortative mating with respect to size. Therefore, the two year classes were not reproductively isolated. Various mechanisms for the determination of life cycle type were discussed with the most likely a cut-off conditional mechanism.
Thesis (Ph.D.) -- University of Adelaide, Dept. of Environmental Biology, 2003
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Cronin, Emma R. (Emma Rachel). "Morphology, respiration and energetics of the eggs of the giant cuttlefish, Sepia apama / Emma R. Cronin." 2000. http://hdl.handle.net/2440/19641.

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Bibliography: leaves 126-144.
144 leaves : ill., maps ; 30 cm.
Title page, contents and abstract only. The complete thesis in print form is available from the University Library.
Thesis (Ph.D.)--University of Adelaide, Dept. of Environmental Biology, 2000
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Cronin, Emma R. (Emma Rachel). "Morphology, respiration and energetics of the eggs of the giant cuttlefish, Sepia apama / Emma R. Cronin." Thesis, 2000. http://hdl.handle.net/2440/19641.

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