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Green2009-herbivore monitoring

Green2009-herbivore monitoring.pdf

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Monitoring Functional Groups of Herbivorous Reef Fishes<br />

The majority of parrotfishes are scrapers, including most Hipposcarus and Scarus species (Bellwood<br />

and Choat 1990). They take non-excavating bites and remove algae, sediment and other material by<br />

closely cropping or scraping the reef surface, leaving shallow scrape marks on the reef substratum<br />

(Bellwood et al 2004, Hoey and Bellwood 2008).<br />

Excavating species include Bolbometapon muricatum, Cetoscarus bicolor and all species of the genus<br />

Chlorurus (Bellwood and Choat 1990). They differ from scrapers by taking deeper excavating bites<br />

and removing greater quantities of substrata with each bite (Bellwood and Choat 1990, Hoey and<br />

Bellwood 2008).<br />

Scrapers and small excavators (individuals 35cm SL) of excavating species:<br />

Bolbometapon muricatum, Cetoscarus bicolor and all species of the genus Chlorurus (Bellwood and<br />

Choat 1990). B. muricatum is the largest species of excavating parrotfish on coral reefs (up to 120cm<br />

total length: Bellwood et al 2003), and each individual ingests 5 tonnes of reef carbonate per year,<br />

almost half of which is live coral skeletons (Bellwood et al 2003). Due to the large volume of live and<br />

dead coral this species consumes, it is considered one of most important bioeroders on coral reefs<br />

(Bellwood et al 2003). Four other species of Indo-Pacific parrotfish have also been observed grazing<br />

on live coral skeletons (including Chlorurus microrhinos and C. bicolor), although live corals only<br />

account for a small proportion of their diet (see Key Families and Their Feeding Modes). Other reef<br />

fishes also feed on live corals and their skeletons, including puffers (Arothron species: Myers 1999),<br />

and occasionally porcupinefishes (Diodon species) and triggerfishes (Cole et al 2008). However, they<br />

are not included here because they are generally uncommon in the Asia Pacific Region, and are<br />

unlikely to play significant roles in coral reef resilience.<br />

Because B. muricatum is a coral predator, its role in coral reef resilience is complex. However, this<br />

species is a natural component of coral reefs in the Asia Pacific Region, and in the absence of other<br />

impacts, it is not a threat to coral reef resilience. Unlike other coral predators like crown-of-thorns<br />

starfish and the snail Drupella, B. muricatum does not undergo population outbreaks and cause<br />

serious degradation to coral communities. In fact on relatively unexploited oceanic<br />

reefs, total ingestion rates balance estimated rates of reef growth (Bellwood et al 2003). This species<br />

also tends to target fast growing corals such as Acropora and Pocillopora (Bellwood et al 2003), and<br />

can act as an important agent of intermediate disturbance (Connell 1978) on reefs, contributing to the<br />

maintenance of high biodiversity. While chronic predation by coral-eating fishes (including<br />

parrotfishes) may exacerbate the effects of climate induced bleaching on coral communities (Cole et al<br />

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