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Green2009-herbivore monitoring

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Monitoring Functional Groups of Herbivorous Reef Fishes<br />

Assigning Species to Functional Groups<br />

The practical application of <strong>monitoring</strong> key functional groups of <strong>herbivore</strong>s requires assigning each<br />

species to a functional group in each geographic area. The following is an example of how to assign<br />

species to functional groups, based on a case study for the Asia Pacific Region.<br />

This study focuses on six families of herbivorous reef fishes that each play important roles in coral reef<br />

resilience: Acanthuridae, Ephippidae, Kyphosidae, Pomacanthidae, Labridae (Tribe Scarini) and<br />

Siganidae (see Key Families and Their Feeding Modes). Other herbivorous reef fishes are not<br />

included because:<br />

• Small, cryptic families (blennies and gobies) are not amenable to visual census techniques,<br />

and are unlikely to make a significant contribution in terms of ecosystem resilience.<br />

• Damselfishes are small, and hard to identify. They also comprise a wide variety of diets<br />

(<strong>herbivore</strong>s, detritivores, algae grazers and planktivores), and it is a complex and difficult task<br />

to assign them to functional groups. Species that are herbivorous also tend to be small and<br />

contribute less in terms of ecosystem resilience, because they are territorial and farm algae<br />

for their own consumption (see Territorial Behaviour).<br />

• While some filefishes, triggerfishes and a wrasse (Pseudodax mollucanus: Cowman et al in<br />

press) may be <strong>herbivore</strong>s, their trophic status has not been confirmed (Myers 1999, Randall et<br />

al 1996, G.P Jones unpubl. data).<br />

A species list for each family in the Asia Pacific Region was provided by Dr. Gerry Allen (Allen et al<br />

2003). Each species was assigned to a functional group (see Functional Groups above) based on the<br />

best available literature, and expert opinion (Table 1). Species that did not belong to one of these<br />

functional groups were deleted, including species that feed exclusively on detritus (Ctenochaetus<br />

species) or plankton (some Acanthurus and Naso species: see Key Families and Their Feeding<br />

Modes).<br />

Ontogenetic changes in diet were taken into account for some species (see Ontogenetic Changes in<br />

Feeding Modes). For example, only juveniles of some species of unicornfishes were included,<br />

because they undergo an ontogenetic change from browsers to planktivores at around 20cm SL.<br />

However, ontogenetic changes in parrotfishes from carnivory to herbivory were not considered,<br />

because this change occurs at such a small size (32mm SL: Bellwood 1988) that juvenile parrotfishes<br />

that are still carnivores would not be counted using underwater visual census methods (see Monitoring<br />

Methods below).<br />

These species will provide the basis of a <strong>monitoring</strong> program for key functional groups of <strong>herbivore</strong>s<br />

on reefs in the Asia Pacific Region.<br />

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