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Plate showing distinct colour phases of (a) footballer, (b) transitional and (c) blue-spot Plectropomus laevis. Scale bars = 5 cm.  

Plate showing distinct colour phases of (a) footballer, (b) transitional and (c) blue-spot Plectropomus laevis. Scale bars = 5 cm.  

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Article
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Species in the coral trout complex Plectropomus spp. are some of the most desired and exploited in the Indo-Pacific, although data are limited for most species. Demographic parameters of blue-spot coral trout, Plectropomus laevis, were estimated on the basis of specimens collected from five regions of the Great Barrier Reef and Torres Strait, Austr...

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... colour phases M. R. are related to size at sexual maturity. Smaller individuals typi- cally have the 'footballer' form characterised by a white body with black saddles, yellow fin markings and few blue spots, whereas larger individuals generally display the 'blue-spot' form with a dark brown or red body covered with distinctive large blue spots (Fig. 2). The two colour phases generally are distinct, but transitional individuals have been observed (Davies et al. 2006). This colour dimorphism is peculiar to P. laevis within the coral trout complex. Other members of the coral trout complex dis- play depth-related colour variation, from dark olive in shallow water to crimson red in deeper ...

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... The spawning patterns found in this study indicate P. maculatus contrasts with other reef fishes with restricted summer recruitment periods [1,10,22,56]. They also contrast with courtship and aggregating behaviours, spawning observations, recruitment observations and histological studies of other Plectropomus spp. on the GBR, which have been documented around new moon phases in spring and summer [36,[57][58][59][60][61][62]. However, all studies except those of Samoilys [36] and Heupel et al. [62] were restricted to spring and summer months (September to February), suggesting winter spawning events may have been missed. ...
... They also contrast with courtship and aggregating behaviours, spawning observations, recruitment observations and histological studies of other Plectropomus spp. on the GBR, which have been documented around new moon phases in spring and summer [36,[57][58][59][60][61][62]. However, all studies except those of Samoilys [36] and Heupel et al. [62] were restricted to spring and summer months (September to February), suggesting winter spawning events may have been missed. While P. leopardus and P. laevis both exhibit clear seasonal spawning in late spring and early summer on the central and northern GBR [36,62], both studies also indicate some spawning activity during other times of year, which support our findings. ...
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... Our results also show that P. laevis have slower growth rates, are longer lived and have lower total mortality rates than any other species of coral grouper, consistent with previous studies where growth has been characterized (Frisch et al., 2016;Grandcourt, 2002;Heupel et al., 2010). These life history traits are likely to translate to slower population turnover rates and make P. laevis inherently more vulnerable to fishing and slower to recover relative to other species of coral grouper. ...
... given that historical collections were made on hook and line (Heupel et al., 2010;Mapstone et al., 2004) and contemporary collections were largely made using spear guns. It is possible that the 80 lbs hand-lines used may not have been capable of landing exceptionally large fish, thereby underestimating mean maximum lengths of P. laevis in the GBRMP. ...
... Contrasting patterns of growth have also been measured for populations of coral grouper in other locations, including P. leopardus from the GBR (Ferreira & Russ, 1994) and Japan (Ebisawa, 2013), P. laevis from the Seychelles (Grandcourt, 2002) and P. laevis from the GBR (Heupel et al., 2010), with estimates of growth rate and asymptotic length being larger than our estimates in all cases. However, we emphasize caution when comparing growth parameters among models when sizes at settlement were not constrained to a common value. ...
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... length) than the more abundant and widespread P. leopardus (matures at 2 to 3 yr; ~60 cm max. length) (Ferreira 1995, Heupel et al. 2010. Additionally, P. laevis undergoes a dramatic colour transition from footballer (white/yellow/ black) to blue-spot (dark with large blue spots) phase upon reaching ~30 cm (~1:1 footballer:blue-spot at 50 cm; Heupel et al. 2010). ...
... length) (Ferreira 1995, Heupel et al. 2010. Additionally, P. laevis undergoes a dramatic colour transition from footballer (white/yellow/ black) to blue-spot (dark with large blue spots) phase upon reaching ~30 cm (~1:1 footballer:blue-spot at 50 cm; Heupel et al. 2010). Both species overlap in distribution, but little is known about resource and habitat selection, particularly for P. laevis, which remains poorly studied. ...
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Prey selection can influence interactions among species, the composition and abundance of prey, and ultimately the movement of energy within the ecosystem. Different species of the exploited coral trout (Plectropomus spp.) often co-occur in reef environments, but their foraging behaviour and ecological niches are largely unknown. To explore niche overlap and resource use of sympatric adult coral trout, stable isotopes (δ13C and δ15N) were quantified for three tissues (muscle, red blood cells, plasma) collected between August 2013 and February 2014 from P. leopardus (n = 117) and P. laevis (n = 36) at four reefs in eastern Australia. Bayesian standard ellipses were used to show that prey selection of P. leopardus varied considerably from P. laevis, particularly the blue-spot colour phase. Size of adult individuals had little influence on δ13C and δ15N values for P. leopardus and both footballer and blue-spot colour phases of P. laevis. Spatio-temporal comparisons of P. leopardus trophic positions, made by adjusting baseline algae and planktonic δ15N at each reef and sampling period, demonstrated that trophic positions varied in time and space, and warrants further investigations. This study highlights that sympatric species of coral trout have distinct ecological roles and will likely react differently to environmental disturbances and/or changes in habitat/prey composition.
... Due to its widespread abundance and value overseas, scientific research, stock assessments, and commercial logbooks have concentrated on P. leopardus or grouped all species together for simplicity despite biological differences. For example, P. laevis, the second most abundant 'coral trout' species at mid-shelf and offshore reefs (Ayling and Choat 2008), grows larger (~100 cm max length) and matures earlier (~1 year) than P. leopardus (matures at 2-3 years; ~60 cm max length) (Ferreira 1995;Heupel et al. 2010), yet no prior study has specifically investigated resource use or movement patterns of P. laevis. ...
... Although P. leopardus stocks appear to be healthy (Leigh et al. 2014), there is growing concern that over-exploitation (Little et al. 2005;McLean et al. 2011), climate change (Johansen et al. 2015), and extreme weather events (Tobin et al. 2010) will adversely affect sustainability. Similarly, P. laevis is currently listed as 'Vulnerable' on the IUCN Red List and without sufficient data, effective management strategies are not possible (Heupel et al. 2010). Considering the relative importance of the 'coral trout' fishery and concerns about its future, there is a large gap in knowledge relating to interactions between sympatric species and potential ecological and humanassociated impacts. ...
... depth sensors followed tidal influences alone), the affected portion of data was removed. Logistic regression (binomial family with logit function) tested whether the inclusion Table 1 Sampling summary of P. laevis and P. leopardus including mean (±SE) size, days at liberty, and the number of days detected (numbers in brackets the range) for those individuals that were analysed Only individuals that were detected ≥25 times and for ≥15 days were analysed a Of the three individuals not analysed here, one was not included because it was mainly detected on the reef flat b These two individuals were not used in inter-reef comparisons or presence measurements c Of the 22 individuals not analysed here, two were not included because they were mainly detected on the reef flat d Lodestone individuals were not included in inter-reef comparisons e The size of maturity of P. leopardus and P. laevis is ~300 mm (Ferreira 1995;Heupel et al. 2010 (presence) or removal (absence) of individuals from data analysis was influenced by release distance from a receiver, the size of fish, reef, or release location (i.e. each reef divided into four sections, each containing two receivers: north-east, south-east, north-west, south-west). Validated detections were grouped into 2-h intervals to reduce effects of autocorrelation between consecutive time periods and to estimate individual locations using a position averaging algorithm (see below). ...
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Understanding spatial distribution and temporal variation in movement patterns of closely related species is relevant for deciphering how resources are selected and whether interactions between species affect resource use patterns. The horizontal space use and vertical space use of two exploited reef fish, Plectropomus leopardus and P. laevis (all adults), were compared at mid-shelf Helix Reef and Lodestone Reef in the Great Barrier Reef over ~3 years using passive acoustic telemetry. Both species were detected throughout the 12-month duration of transmitters (mean detection period: ~270 days) and often made deep movements to ~40 m possibly related to reproductive behaviour (spawning). Differences in space use were apparent between species, with P. laevis consistently using greater area around reefs throughout the year. Overall, depth use patterns were similar between species; however, when daily detections were grouped in 2-h periods, P. laevis remained shallower and had greater variation in depth
... A total of 11 publications on 4 plectropomids were used (Currey et al., 2010, Ebisawa, 2013Ferreira and Russ, 1992;Grandcourt, 2005;Heupel et al., 2010b;Loubens, 1978Loubens, , 1980aRuss et al., 1998;Rhodes et al., 2013;Williams et al., 2008) to develop 8 estimates of L m /L ∞ and 14 estimates of M/k (Table A4). Five published studies on 2 Variola species (V. ...
... However for both sectors coral trout made up 66% of the total harvest by weight probably due to the TIB sector taking significantly more blue spot coral trout (Plectropomus laevis) than the TVH sector (Williams et al. 2008a). P. laevis are the largest of the coral trout species (Heupel et al. 2010). For both sectors P. leopardus is the major species harvested at around 80% of all coral trout. ...
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Full-text available
The squaretail coralgrouper Plectropomus areolatus was identified as a fast-growing, early maturing and relatively short-lived aggregation-spawning epinephelid. Examinations of sectioned otoliths found females and males first maturing at 2 and 3 years, respectively, suggesting protogynous hermaphroditism; however, no transitionals were observed in samples. Age distribution for the two sexes was similar and both were represented in the oldest age class; however, significant sex-specific differences in size-at-age were identified. Both sexes fully recruit into the fishery at age 4 years and reach 90% of asymptotic length by age 3 years. Underwater visual assessments, combined with the gonado-somatic indices, revealed a 5 month reproductive season, with interannual variability observed in the month of highest density within the spawning aggregation. Catch restrictions on adults during spawning times and at reproductive sites, combined with gear-based management and enhanced enforcement, are recommended to maintain spawning stocks. Based on the available evidence, the sexual pattern for this species is unresolved.
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Article
Full-text available
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