The sizes of E. fuscoguttatus aggregating in Kenya conform to those of reproductively active E.fuscoguttatus on the Great Barrier Reef (GBR), Australia. Pears et al. (2006) report that this speciesis a long-lived protogynous hermaphrodite with males ranging in size from 68.3 to 92.5 cm TLand mature females from 32.0 to 85.5 cm TL. No fish smaller than 56-60 cm TL was observedat the Kenyan aggregations. The change in size frequency distribution at the aggregation sitesbetween the summer <strong>spawning</strong> and non-<strong>spawning</strong> winter period, with fish greater than 90 cm TLonly observed during November-January suggests that the largest males migrate to the aggregationsites to spawn. These may be the males that dominate gaining access to females, as seen in othergroupers (Samoilys and Squire 1994, Samoilys 1997b, Robinson et al. 2008b).Management implicationsE. fuscoguttatus demography of long life (40+ years), late onset of sexual maturity in females (at 9years), increasing female fecundity with age over a reproductive lifespan of more than 30 yr (Pearset al. 2006) do not confer resilience to fishing. In fact, such life history traits are all closely correlatedwith vulnerability to extinction (Mace and Hudson 1999; Reynolds et al. 2003; Dulvy et al 2003).These demographic factors, coupled with heavy fishing pressure and the many unmanaged fisheriesfor this grouper, led to its Near Threatened classification on the Red List (IUCN 2011). Thefact that E. fuscoguttatus also forms <strong>spawning</strong> aggregations that appear to be predictable in timeand place increases the vulnerability of this species (Sadovy de Mitcheson et al. 2008). This isparticularly so in Kenya where coastal fishing is not regulated by size class (both minimum andmaximum size class fishery restrictions would be beneficial for this species). Additionally, the fullyprotected marine areas (the nationally gazetted Marine Parks) are small, protecting only 8.6% of thecountry’s coral reef area (Spalding 2001; Wells 2006) in contrast with global recommendations inthe order of 30% (Fernandes et al. 2005). Recent reports of reproductive movement and estimatesof catchment area for this species suggest large-scale marine parks are needed to protect populationsof this species (Rhodes et al. 2012).Local artisanal catches of E. fuscoguttatus have dwindled in recent years (see Chapter 3; Samoilyset al. 2011b) to the extent that we were unable to collect adequate gonads for reproductiveassessment, or assess population abundance through catch rate analysis. Population abundancesurveys (on SCUBA to 30 m) on eastern African reefs also show that this species is rare (Samoilysunpubls. data), possibly in response to historical targeted fishing of aggregations of this species. Ourindicator-based vulnerability analysis of the <strong>spawning</strong> aggregations of this species also revealed thatthey have relatively high vulnerability (see Chapter 11).Given the combined factors of life history, small aggregation size and low cover of protected areasat a national scale, there is a need to institute additional management if this species is to persistalong the southern Kenyan coastline. The aggregation sites documented here are not managed orprotected, despite one occurring within the nationally gazetted Diani-Chale Reserve. This Reserveis not enforced due to strong local opposition from fishers. Low aggregation sizes may be theresult of past fishing at aggregation sites or on the population as a whole. Further, we know fromstudies in Australia (Pears et al. 2006, 2007) that E. fuscoguttatus females need to breed for 30+years to reach their full reproductive potential and our results suggest that <strong>spawning</strong> aggregationsare important sites for these females to spawn. We therefore recommend that management of thesesites be discussed as a matter of priority with all stakeholders, including local fishing communities,the hotel/dive tourism industry and the government’s Kenya Wildlife Service (KWS) with authorityover the Diani-Chale Reserve. Conflict between different users in this area has been ongoing formany years, but recent mitigation training and discussions have provided options for resolvingthese difficulties (Watson and Ater 2011). To protect this valuable and threatened grouper, it isimportant that management options, including permanent no-take zones, are discussed for the<strong>spawning</strong> aggregation sites within the Reserve.74
Chapter 8: Spawning aggregation dynamics ofbrown-marbled, Epinephelus fuscoguttatus (Forsskål,1775) and camouflage grouper, E. polyphekadion(Bleeker, 1849) at a mixed-species aggregation siteJude Bijoux, Jan Robinson and Laurent DagornIntroductionThe global catch of wild groupers is close to 200,000 tons (Tupper and Sheriff 2008) and marketdemand continues to increase, especially within the Southeast Asia-based Live Reef Food Fish Trade(LRFFT). Camouflage (Epinephelus polyphekadion) and brown-marbled grouper (E. fuscoguttatus)are two important high value food fishes that are targeted by large-scale commercial (LRFFT) andsmall-scale reef fisheries throughout much of the Indo-Pacific (Sadovy 2005). Found in coral richareas down to depths of 60 m, both species are voracious ambush predators that are slow growing,late maturing and occur at low densities throughout much of their range (Russell et al. 2006;Pears 2012) except during <strong>spawning</strong> aggregations (Sadovy 2005). Epinephelus fuscoguttatus has asexual pattern corresponding to protogynous hermaphrodism (Pears et al. 2006; 2007) while E.polyphekadion is gonochoristic with the potential for sexual transition (Rhodes et al. 2011). Bothspecies spawn in mixed-species transient <strong>spawning</strong> aggregations of <strong>10</strong>0s to <strong>10</strong>00s of individualsthat are ephemeral in nature and spatially and temporally predictable (Pears 2012; Rhodes et al.2012). These life history traits make both species highly susceptible to even low levels of fishing. Inmany places, the location and timing of these aggregations are known by fishers and they have beenheavily targeted, leading to stock decline (Sala et al. 2001), demographic changes (e.g. Beets andFriedlander 1998; Rhodes et al. 2011), and in extreme cases, the total disappearance or reproductivefailure of aggregating populations (Johannes et al. 1999; Mangubhai et al. 2011).Spawning aggregations of E. polyphekadion and E. fuscoguttatus have been verified at an atoll inthe southern Seychelles. At one of the atoll aggregation sites, marbled coral grouper, Plectropomuspunctatus, also forms <strong>spawning</strong> aggregations during the same period. Recent research hashighlighted an urgent need to assess management requirements at <strong>spawning</strong> aggregation sitesvulnerable to fishing in the WIO. At the study atoll in Seychelles, there is a basic understanding ofthe spatial and temporal dynamics of E. fuscoguttatus and E. polyphekadion aggregations at one oftheir known <strong>spawning</strong> sites (Robinson et al. 2008b). A stakeholder-driven process between 2003and 2006 recommended the establishment of closed seasons or fishery reserves to protect the coreaggregation sites at the atoll. Though formal management of the aggregation sites has yet to beadopted, stakeholders voluntarily ceased fishing the aggregation sites during the <strong>spawning</strong> periodfrom 2005. This informal approach requires both spatial and temporal information on aggregationdynamics. Critical gaps in knowledge are known to undermine the current management andinclude fidelity to the sites, precise estimates of aggregation duration and periodicity, and thelocation of migration routes and catchment area (the area from which reproductive individuals aredrawn). Major migration pathways in relation to the aggregation sites have not been identified, butare reported to exist in other locales for these species (Rhodes et al. 2012).In this study, we applied passive acoustic telemetry to provide information on key <strong>spawning</strong>aggregation parameters. The technology enabled detection of tagged fish at <strong>spawning</strong> sitesinstrumented with acoustic receivers for periods of over one year. We make use of the detectionsto study the dynamics of camouflage and brown-marbled grouper over two <strong>spawning</strong> seasons andseveral <strong>spawning</strong> months. We specifically looked at the seasonal, lunar and diel timing of arrivalsand departures at the fish <strong>spawning</strong> aggregation (FSA) site, <strong>spawning</strong> site residency times andfidelity, and the identification of catchment area for the sites.75
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The designation of geographical ent
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Chapter 1: IntroductionJan Robinson
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limited, subsistence levels of expl
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NTRs for spawning aggregations usin
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al. 2003). Verification may include
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a fraction of spawning sites are pr
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Chapter 3: Targeted fishing of the
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verifying spawning aggregations, we
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(a)(b)Fig. 3. Spatial patterns ofca
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during full moon periods. Siganus s
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model, many parameter estimates are
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ReferencesAbunge C (2011) Managing
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Cox DR (1972) Regression models and
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Grüss A, Kaplan DM, Hart DR (2011b
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Kaunda-Arara B, Rose GA (2004a) Eff
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Newcomer RT, Taylor DH, Guttman SI
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Sancho G, Petersen CW, Lobel PS (20
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Appendix 1. QuestionnaireMASMA SPAW
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8. Spawning aggregation knowledgeUs
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Example items KSh Furthest site Clo
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Appendix II. Experimental testing o
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Clove oil concentrationAt a concent
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Appendix III. Application of acoust
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