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Thematische Bibliographien / Pagrus auratus / Zeitschriftenartikel

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Zeitschriftenartikel zum Thema „Pagrus auratus“

Autor: Grafiati

Veröffentlicht am 4. Juni 2021

Zuletzt aktualisiert am 20. Februar 2023

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1

Francis, Malcolm P. „Growth of juvenile snapper,Pagrus auratus“. New Zealand Journal of Marine and Freshwater Research 28, Nr. 2 (Juni 1994): 201–18. http://dx.doi.org/10.1080/00288330.1994.9516608.

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2

Francis, M. P. „Condition cycles in juvenile Pagrus auratus“. Journal of Fish Biology 51, Nr. 3 (September 1997): 583–600. http://dx.doi.org/10.1111/j.1095-8649.1997.tb01514.x.

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3

Tabata, Kazuo, und Nobuhiko Taniguchi. „Differences between Pagrus major and Pagrus auratus through mainly mtDNA control region analysis“. Fisheries Science 66, Nr. 1 (Februar 2000): 9–18. http://dx.doi.org/10.1046/j.1444-2906.2000.00032.x.

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4

Robinson, Esme, Alistair Jerrett, Suzanne Black und William Davison. „Hypoxia impairs visual acuity in snapper (Pagrus auratus)“. Journal of Comparative Physiology A 199, Nr. 7 (17.03.2013): 611–17. http://dx.doi.org/10.1007/s00359-013-0809-7.

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5

Otway, N. M., J. R. Craig und J. M. Upston. „Gear-dependent size selection of snapper, Pagrus auratus“. Fisheries Research 28, Nr. 2 (September 1996): 119–32. http://dx.doi.org/10.1016/0165-7836(96)00500-0.

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6

Radford, C. A., C. J. Sim-Smith und A. G. Jeffs. „Can larval snapper, Pagrus auratus, smell their new home?“ Marine and Freshwater Research 63, Nr. 10 (2012): 898. http://dx.doi.org/10.1071/mf12118.

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The ability to find a suitable settlement habitat after a pelagic larval period represents a significant challenge to marine settlement-stage larvae, and the mechanisms by which they achieve this are poorly understood. There is good evidence that olfactory cues are used by some coral reef fish larvae to locate suitable settlement habitats; however, the same understanding is lacking for marine temperate fish. Here we show for the first time that the larvae of an important commercial and recreational marine temperate fish, Pagrus auratus, can use olfactory cues to orient to appropriate settlement habitat. Using pairwise choice experiments, naive hatchery reared fish were offered water collected from a range of habitats in the Kaipara Harbour, an important nursery area for P. auratus. Larvae selected to swim towards water taken from over seagrass beds, their preferred settlement habitat, than water taken from the harbour entrance, Asian date mussel habitat, artificial seawater or artificial seawater in which seagrass had been soaked. The preference by the fish for water from the seagrass habitat over artificial seawater in which seagrass had been soaked strongly suggests that chemical cues from sources other than seagrass, such as from prey or conspecifics present in the seagrass habitat, may also be involved.

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7

Terauchi, Kumiko, Takashi Matsumoto und Nozomu Hirota. „Purification of AMP Deaminase from Muscle of Snapper Pagrus auratus.“ NIPPON SUISAN GAKKAISHI 58, Nr. 11 (1992): 2069–73. http://dx.doi.org/10.2331/suisan.58.2069.

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8

Meggs, L. B., C. M. Austin und P. C. Coutin. „Low allozyme variation in snapper, Pagrus auratus , in Victoria, Australia“. Fisheries Management and Ecology 10, Nr. 3 (19.05.2003): 155–62. http://dx.doi.org/10.1046/j.1365-2400.2003.00332.x.

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9

Francis, MP, MW Williams, AC Pryce, S. Pollard und SG Scott. „Daily incuremtns in Otoliths of juvenile Snapper, Pagrus auratus (Sparidae)“. Marine and Freshwater Research 43, Nr. 5 (1992): 1015. http://dx.doi.org/10.1071/mf9921015.

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Sagitta microstructure was investigated in juvenile New Zealand snapper, Pagrus auratus, to provide a basis for daily ageing in population dynamics studies. Transverse sections produced the clearest daily increments and were the easiest to prepare. Daily increment formation was validated up to an age of 100 days by using increment counts from reared juveniles and up to about 160 days by using changes in mean increment counts from juveniles sampled from a wild population at different times. A prominent metamorphic mark was visible in transverse and frontal sections, providing a means for determining the duration of the larval period, and juvenile postmetamorphic ages. Postmetamorphic increment width varied with the age of the snapper and with season. Increment width dropped below 0.5 μm in winter and increments could not be resolved with a light microscope.

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10

Morrison, Richard N., John D. Hayball, Mathew T. Cook und Barbara F. Nowak. „Anti-immunoglobulin binding and activation of snapper (Pagrus auratus) leucocytes“. Developmental & Comparative Immunology 26, Nr. 3 (April 2002): 247–55. http://dx.doi.org/10.1016/s0145-305x(01)00070-2.

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11

Hobby, A. C., und N. W. Pankhurst. „Post-ovulatory egg viability in the snapper Pagrus auratus (Sparidae)“. Marine and Freshwater Research 48, Nr. 5 (1997): 385. http://dx.doi.org/10.1071/mf96120.

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The role of gonadal steroids in maintaining post-ovulatory egg viability was investigated in the snapper (Pagrus auratus), a daily-repeat-spawning teleost. Ovulated eggs were held in vitro in L15 medium, or in L15 medium supplemented with gonadal steroids or gonadotrophin, to investigate any direct effects of reproductive hormones on post-ovulatory egg viability. The viability of eggs retained in the oviduct decreased with increasing time after ovulation, to give fertilization of below 50% after 6 h. The viability of eggs held in L15 medium was at least as good at that of eggs held in vivo. Storage of eggs in L15 medium supplemented with the reproductive hormones testosterone, 17α-hydroxyprogesterone, 17α,20β-dihydroxy-4-pregnen-3-one and human chorionic gonadotrophin did not improve or reduce viability relative to controls, suggesting that the hormones investigated have no direct effect on post-ovulatory egg viability.

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12

Francis, M. P., und M. W. Williams. „Diel variation in trawl catch rates of Pagrus auratus (Sparidae)“. Fisheries Research 24, Nr. 4 (November 1995): 301–10. http://dx.doi.org/10.1016/0165-7836(95)00384-5.

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13

Nowak, BF, und SC Battaglene. „Incidence and Composition of Calculi in the Urinary Bladder of Intensively Reared Marine Fish Larvae“. Marine and Freshwater Research 47, Nr. 2 (1996): 255. http://dx.doi.org/10.1071/mf9960255.

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Calculi were observed in the urinary tracts of a wide range of intensively reared marine fish larvae at the Port Stephens Research Centre. Data are presented for three species: snapper Pagrus auratus, mulloway Argyrosomus hololepidotus, and Australian bass Macquaria novemaculeata. Calculi first appeared in P. auratus on Day 5 after hatching, in M. novemaculeata on Day 11, and in A. hololepidotus on Day 12. Around 80% of larvae typically had calculi after two weeks of intensive rearing. No relationship could be found between the absence of the functional swim bladder and the presence of calculi in all species studied. The presence of calculi did not stop the larvae of any species from actively feeding on live prey. Calculi from M. novemaculeata and P. auratus were analysed with an electron probe microanalyser. Phosphorus and calcium were detected in all calculi, usually accompanied by magnesium. Potential causes for the formation of calculi are discussed.

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14

Broadhurst, M. K., P. A. Butcher, K. C. Hall, B. R. Cullis und S. P. McGrath. „Resilience of inshore, juvenile snapper Pagrus auratus to angling and release“. Journal of Fish Biology 80, Nr. 3 (März 2012): 638–50. http://dx.doi.org/10.1111/j.1095-8649.2011.03202.x.

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15

Bell, J. D., N. Quartararo und G. W. Henry. „Growth of snapper,Pagrus auratus, from south‐eastern Australia in captivity“. New Zealand Journal of Marine and Freshwater Research 25, Nr. 2 (Juni 1991): 117–21. http://dx.doi.org/10.1080/00288330.1991.9516461.

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16

Canfield, P. J., N. Quartararo, D. L. Griffin, G. N. Tsoukalas und S. E. Cocaro. „Haematological and biochemical reference values for captive Australian snapper, Pagrus auratus“. Journal of Fish Biology 44, Nr. 5 (Mai 1994): 849–56. http://dx.doi.org/10.1111/j.1095-8649.1994.tb01259.x.

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17

DURHAM, PJK, MJ ALLANSON und WG HUTCHINSON. „Lymphocystis disease in snapper (Pagrus auratus) from Spencer Gulf, South Australia“. Australian Veterinary Journal 74, Nr. 4 (Oktober 1996): 312–13. http://dx.doi.org/10.1111/j.1751-0813.1996.tb13787.x.

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18

Quartararo, N., G. L. Allan und J. D. Bell. „Replacement of fish meal in diets for Australian snapper, Pagrus auratus“. Aquaculture 166, Nr. 3-4 (Juli 1998): 279–95. http://dx.doi.org/10.1016/s0044-8486(98)00289-0.

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19

Leach, Foss, und Janet Davidson. „Pre-European Catches of Snapper (Pagrus auratus) in Northern New Zealand“. Journal of Archaeological Science 27, Nr. 6 (Juni 2000): 509–22. http://dx.doi.org/10.1006/jasc.1999.0474.

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20

Kingsford, MJ, und MH Atkinson. „Increments in otoliths and scales: How they relate to the age and early development of reared and wild larval and juvenile Pagrus auratus (Sparidae)“. Marine and Freshwater Research 45, Nr. 6 (1994): 1007. http://dx.doi.org/10.1071/mf9941007.

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The utility of otoliths and scales for age and growth studies on Northern and Southern Hemisphere forms of Pagrus auratus (<I00 days old) was investigated. A series of illustrations shows the developmental morphology of wild southern larvae at ages ranging from 0 to 40 days. Reared P. Auratus (of both forms) deposited daily increments in otoliths from or within 1 day of the time of hatching until the age of 40 days. Age-length relationships of wild P auratus (2.4-8.5 mm standard length, SL) from northern New Zealand (1985-86) were not significantly different among times and there was little variation in length at age among fish. In contrast, great variation in age-length relationships was found for reared larvae (5-30 days old). The data suggest that slow-growing fish may suffer high mortality rates in the wild. On the basis of age-length relationships of wild P. auratus, recommendations are made for appropriate sampling frequency in studies of larval abundance. Ctenoid scales formed at 8-9 mm SL in both forms of P. auratus. The number of increments in newly settled P. auratus (<60 days old) closely approximated the number of days since scale formation (i.e. t 2 5 circuli). This may provide a new method for estimation of the timing of a concurrent change in the behaviour of some fish larvae (e.g. a change in vertical distribution). Importantly, the number of circuli was correlated with the growth of juveniles, just as the spacing of circuli is in other species. Thus, circuli in scales potentially provide a history of individual growth in small fish after the formation of scales (to 100 days old) and an indication of the time since scales appeared.

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21

Lam, Ho Son, und Huynh Minh Sang. „TỔNG QUAN VỀ VIỆC SỬ DỤNG SELEN (Se) TRONG NUÔI TRỒNG THỦY SẢN“. Tạp chí Khoa học và Công nghệ Biển 18, Nr. 2 (30.06.2018): 214–21. http://dx.doi.org/10.15625/1859-3097/18/2/8949.

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Effects of antibiotics usage in aquaculture on environment and human health has prompted the search for alternative products. Recently, the microelements in organic form have been used as alternative to antibiotics in aquaculture. Se is one of the microelements that have received heightened attention. This report reviews the role of Se in the culture of fishes (cobia Rachycentron canadum L., red sea bream Pagrus major, fingerling channel catfish Ictalurus punctatus, seabass Lates calcarifer, snubnose dart Trachinotus blochii, rainbow trout Oncorhynchus mykiss, common carp Cyprinus carpio L., Atlantic salmon parr Salmo salar, nile tilapia Oreochromis niloticus, african catfish Clarias gariepinus, Senegalese sole Solea senegalensis, grouper Epinephelus malabaricus, gilthead seabream Sparus aurata, Chinook salmon Oncorhynchus tshawytscha, fathead minnow Pimephales promelas, striped bass Morone saxatilis, bluegill Lepomis macrochirus, crucian carp Carassius auratus gibelio) and crustacean (giant freshwater prawn Macrobrachium rosenbergii, white shrimp Penaeus vannamei, marron Cherax cainii, crayfish Procambarus clarkii). Suggestion for further research on the application of Se in aquaculture is also included.

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22

Otway, NM, und JR Craig. „Effects of hook size on the catches of undersized snapper Pagrus auratus“. Marine Ecology Progress Series 93 (1993): 9–15. http://dx.doi.org/10.3354/meps093009.

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23

Le Port, A., JC Montgomery und AE Croucher. „Biophysical modelling of snapper Pagrus auratus larval dispersal from a temperate MPA“. Marine Ecology Progress Series 515 (18.11.2014): 203–15. http://dx.doi.org/10.3354/meps10973.

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24

Robinson, E., A. R. Jerrett, S. E. Black und W. Davison. „Visual acuity of snapper Pagrus auratus: effect of size and spectral composition“. Journal of Fish Biology 79, Nr. 7 (15.11.2011): 1883–94. http://dx.doi.org/10.1111/j.1095-8649.2011.03130.x.

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25

Thurstan, Ruth H., Alexander B. Campbell und John M. Pandolfi. „Nineteenth century narratives reveal historic catch rates for Australian snapper (Pagrus auratus)“. Fish and Fisheries 17, Nr. 1 (24.10.2014): 210–25. http://dx.doi.org/10.1111/faf.12103.

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26

Majed, S. A., R. M. G. Wells und B. H. Mcardle. „Seasonal effect on lactate dehydrogenase and citrate synthase in snapper (Pagrus auratus)“. New Zealand Journal of Marine and Freshwater Research 36, Nr. 1 (März 2002): 233–39. http://dx.doi.org/10.1080/00288330.2002.9517082.

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27

Millar, Russell B., Brian H. McArdle und Shelton J. Harley. „Modeling the size of snapper (Pagrus auratus) using temperature-modified growth curves“. Canadian Journal of Fisheries and Aquatic Sciences 56, Nr. 7 (01.07.1999): 1278–84. http://dx.doi.org/10.1139/f99-057.

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Age-length keys from RV Kaharoa trawl surveys in the years 1984-1990 and 1992-1994 were used to estimate mean lengths-at-age of snapper (Pagrus auratus) in the Hauraki Gulf of New Zealand. A von Bertalanffy growth curve fitted to these lengths-at-age exhibited poor fit, and when the fit was restricted to only cohorts since 1968 (those for which sea surface temperature data were available) the estimated maximum length parameter dropped 5 cm. A power curve provided a better fit without an increase in the number of parameters and was not sensitive to the restriction to younger cohorts. When water temperature was added to the power curve model the residual plots indicated unexplained year effects and temporal correlation. These features were included using a mixed-effects model for repeated-measures data, and temperature was found to be statistically significant (p < 0.0001). This conclusion was corroborated via a simple randomization test. The model predicts growth over a year to change by the equivalent of 8 weeks if the average annual water temperature changes by 1°C. This is sufficient to predict a 4-year-old snapper from the 1986 cohort as having the equivalent of 6 months more growth (at the growth rate corresponding to average water temperature) than a 4-year-old fish from the 1990 cohort.

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28

Fielder, D. Stewart, William J. Bardsley, Geoff L. Allan und Patricia M. Pankhurst. „Effect of photoperiod on growth and survival of snapper Pagrus auratus larvae“. Aquaculture 211, Nr. 1-4 (August 2002): 135–50. http://dx.doi.org/10.1016/s0044-8486(02)00006-6.

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29

West, A. P., und F. R. Roubal. „Population dynamics of the monogenean Anoplodiscus cirrusspiralis on the snapper, Pagrus auratus“. International Journal for Parasitology 28, Nr. 4 (April 1998): 571–77. http://dx.doi.org/10.1016/s0020-7519(98)00014-9.

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30

Gagnon, Marthe Monique, und Christopher Allan Rawson. „Diuron increases spinal deformity in early-life-stage pink snapper Pagrus auratus“. Marine Pollution Bulletin 58, Nr. 7 (Juli 2009): 1083–85. http://dx.doi.org/10.1016/j.marpolbul.2009.04.011.

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31

Parsons, Darren M., Mark A. Morrison und Matthew J. Slater. „Responses to marine reserves: Decreased dispersion of the sparid Pagrus auratus (snapper)“. Biological Conservation 143, Nr. 9 (September 2010): 2039–48. http://dx.doi.org/10.1016/j.biocon.2010.05.009.

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32

Ferrell, DJ, GW Henry, JD Bell und N. Quartararo. „Validation of annual marks in the Otoliths of young Snapper, Pagrus auratus (Sparidae)“. Marine and Freshwater Research 43, Nr. 5 (1992): 1051. http://dx.doi.org/10.1071/mf9921051.

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In April 1989, young-of-the-year snapper (Pagrus auratus) were captured from the wild and injected with tetracycline. The fish were reared on natural food in a large pool with flowing sea water under ambient marine conditions. Two fish were removed every two months for two years, and the growth of their otoliths, relative to the tetracycline mark, was measured. Growth of the otoliths was greatest in spring and summer and least during winter. Opaque marks appeared in the otoliths of fish during both winters of the study. Our results confirm that the opaque marks in otoliths of young snapper can be used to determine the age of the fish in years.

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33

Thrush, SF, D. Schultz, JE Hewitt und D. Talley. „Habitat structure in soft-sediment environments and abundance of juvenile snapper Pagrus auratus“. Marine Ecology Progress Series 245 (2002): 273–80. http://dx.doi.org/10.3354/meps245273.

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34

Usmar, NR. „Ontogenetic diet shifts in snapper (Pagrus auratus: Sparidae) within a New Zealand estuary“. New Zealand Journal of Marine and Freshwater Research 46, Nr. 1 (März 2012): 31–46. http://dx.doi.org/10.1080/00288330.2011.587824.

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35

Dyer, A. R., P. de la M Hall und G. I. Matsumoto. „Needle biopsy of liver in a marine teleost, Pagrus auratus (Bloch & Schneider)“. Journal of Fish Diseases 20, Nr. 6 (November 1997): 463–66. http://dx.doi.org/10.1046/j.1365-2761.1997.00317.x.

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36

Morison, A. K. „Is rigor mortis the cause of post-mortem shrinkage in juvenile Pagrus auratus?“ Journal of Fish Biology 65, Nr. 3 (September 2004): 883–88. http://dx.doi.org/10.1111/j.0022-1112.2004.00485.x.

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37

Maunder, Mark N., und Paul J. Starr. „Industry participation in stock assessment: the New Zealand SNA1 snapper (Pagrus auratus) fishery“. Marine Policy 26, Nr. 6 (November 2002): 481–92. http://dx.doi.org/10.1016/s0308-597x(02)00046-5.

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38

Francis, RICC. „Otolith radius is a poor predictor of age in Adult Snapper (Pagrus auratus)“. Marine and Freshwater Research 43, Nr. 5 (1992): 1199. http://dx.doi.org/10.1071/mf9921199.

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39

Hartill, B. W., M. A. Morrison, M. D. Smith, J. Boubée und D. M. Parsons. „Diurnal and tidal movements of snapper (Pagrus auratus, Sparidae) in an estuarine environment“. Marine and Freshwater Research 54, Nr. 8 (2003): 931. http://dx.doi.org/10.1071/mf02095.

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Using individually coded acoustic transponders and an array of 15 moored receivers (detection range ~300 m), the temporal and spatial movements of the temperate snapper Pagrus auratus (Sparidae) were studied within an estuary. Of the 28 fish initially tagged, 20 were subsequently detected within the study area for up to 70 days. The spatial scale of daily movements was in the order of hundreds of metres for most fish, suggesting relatively restricted home ranges over the period monitored (November–January). The detectability of fish remaining in the estuary was lower at night, probably because of fish moving out of the main channel and onto surrounding shallow banks during darkness. Temporal movement patterns detected using spectral analyses (Fast Fourier Transforms) were predominantly diurnal, with subordinate tidal behaviour also evident in some fish. These results demonstrate that in this system, snapper occupy relatively small (hundreds of metres) and discrete areas of soft sediment seafloor, within which repeated, predictable movements are made. Variability among fish has highlighted the need for a better understanding of the relationship between fish behaviour and fine-scale habitat features (metres).

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40

Sumpton, Wayne D., Bill Sawynok und Neil Carstens. „Localised movement of snapper (Pagrus auratus, Sparidae) in a large subtropical marine embayment“. Marine and Freshwater Research 54, Nr. 8 (2003): 923. http://dx.doi.org/10.1071/mf02119.

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Snapper were tagged with dart and anchor tags in order to determine movement and the contribution of juveniles inhabiting estuarine areas to the offshore adult population. Laboratory experiments showed that loss of anchor tags was greater than dart tags, although this was not reflected in the results of field trials. A total of 6572 individuals were tagged in field experiments, of which 509 (7.7%) were recaptured. Only four of over 2500 fish tagged and released in Moreton Bay were recaptured in waters outside the bay, suggesting the bay is not an important source of recruits to the offshore fishery. However, problems associated with tag loss and mortality meant that the actual contribution of juveniles to the offshore fisheries remained unclear. Most snapper movements were localised; only ~1% of movements exceeded 100 km. Movements of snapper were mainly directed northward against the prevailing direction of the East Australian Current. Snapper were considered to be a suitable species for marine reserve protection owing to their relatively localised movement patterns.

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41

REDDACLIFF, GL, und N. QUARTARARO. „Lymphocystis in cultured snapper (Pagrus auratus) and wild kingfish (Seriola lalandi) in Australia“. Australian Veterinary Journal 69, Nr. 5 (Mai 1992): 116–17. http://dx.doi.org/10.1111/j.1751-0813.1992.tb07467.x.

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42

Morrison, R. N., und B. F. Nowak. „Affinity purification and partial characterisation of systemic immunoglobulin of the snapper (Pagrus auratus)“. Aquaculture 201, Nr. 1-2 (September 2001): 1–17. http://dx.doi.org/10.1016/s0044-8486(01)00566-x.

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43

Morrison, Richard N., A. Bruce Lyons, Barbara F. Nowak und John D. Hayball. „Assessment of snapper (Pagrus auratus) natural IgM binding to bromelain treated sheep erythrocytes“. Fish & Shellfish Immunology 18, Nr. 1 (Januar 2005): 91–99. http://dx.doi.org/10.1016/j.fsi.2004.06.006.

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44

Ryan, Stuart. „The dynamics of MS-222 anaesthesia in a marine teleost (Pagrus auratus: Sparidae)“. Comparative Biochemistry and Physiology Part C: Comparative Pharmacology 101, Nr. 3 (April 1992): 593–600. http://dx.doi.org/10.1016/0742-8413(92)90092-l.

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45

Stewart, John. „Capture depth related mortality of discarded snapper (Pagrus auratus) and implications for management“. Fisheries Research 90, Nr. 1-3 (April 2008): 289–95. http://dx.doi.org/10.1016/j.fishres.2007.11.003.

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46

Butcher, Paul A., Matt K. Broadhurst, Karina C. Hall, Brian R. Cullis und Shane R. Raidal. „Assessing barotrauma among angled snapper (Pagrus auratus) and the utility of release methods“. Fisheries Research 127-128 (September 2012): 49–55. http://dx.doi.org/10.1016/j.fishres.2012.04.013.

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Kohli, Gurjeet S., G. Giménez Papiol, Lesley L. Rhodes, D. Tim Harwood, Andrew Selwood, Alistair Jerrett, Shauna A. Murray und Brett A. Neilan. „A feeding study to probe the uptake of Maitotoxin by snapper (Pagrus auratus)“. Harmful Algae 37 (Juli 2014): 125–32. http://dx.doi.org/10.1016/j.hal.2014.05.018.

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Parsons, DM, RC Babcock, RKS Hankin, TJ Willis, JP Aitken, RK O'Dor und GD Jackson. „Snapper Pagrus auratus (Sparidae) home range dynamics: acoustic tagging studies in a marine reserve“. Marine Ecology Progress Series 262 (2003): 253–65. http://dx.doi.org/10.3354/meps262253.

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Battaglene, S. C., und R. B. Talbot. „Induced spawning and larval rearing of snapper,Pagrus auratus(Pisces: Sparidae), from Australian waters“. New Zealand Journal of Marine and Freshwater Research 26, Nr. 2 (Juni 1992): 179–85. http://dx.doi.org/10.1080/00288330.1992.9516513.

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Willis, Trevor J., Darren M. Parsons und Russ C. Babcock. „Evidence for long‐term site fidelity of snapper(Pagrus auratus)within a marine reserve“. New Zealand Journal of Marine and Freshwater Research 35, Nr. 3 (September 2001): 581–90. http://dx.doi.org/10.1080/00288330.2001.9517024.

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