Status of Near-Shore Reefs of the Great Barrier Reef 2004
Research Report
Hugh Sweatman, Angus Thompson, Steve Delean, Johnston Davidson
and Steve Neale
Australian Institute of Marine Science
CRC Reef Research Centre Project
C1.14 - Status of near-shore reefs of the Great Barrier Reef
2003-04
ISBN 9781921359019
Published June 2007
Executive Summary
Near-shore reefs of the Great Barrier Reef (GBR) cover only a
small part of the World Heritage Area, but they have
disproportionate significance as signals of the condition of the
ecosystem. These reefs are the most accessible to coastal
communities and they are the most at risk from runoff. While there
have been many studies of near-shore reefs, there has not been a
large-scale systematic assessment of their status. This study had
dual aims: (1) to assess the current status of a large sample of
near-shore reefs along the GBR coast; and (2) to assemble a list of
past studies and incorporate their findings as appropriate.
In 2004, we surveyed the benthic communities at 33 reefs in six
regions between Cape Tribulation (16°S) and Keppel Island
(23°S). Where topography allowed, two depths were surveyed at
replicate sites at each reef giving a total of 63 locations.
Surveys measured benthic cover, community composition, diversity of
coral species and size-structures of coral communities.
Principal findings were as follows:
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The near-shore reef communities were very variable in 2004.
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Coral cover was extremely high in some locations: shallow parts
of the reef slopes on the backs of Middle Island, Halfway Island
and Humpy Islan (Keppel region) had more than 80% cover of living
hard coral. Nearly a quarter of the locations had more than 50%
cover of hard corals. Coral cover was less than 10% at ten
locations. Over all, the average cover of living hard coral was
33%. This is slightly higher than the average cover of 30% from 36
reefs in middle and outer regions of the GBR lagoon that were
surveyed by the Australian Institute of Marine Science (AIMS) in
2004/2005.
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The number of species of hard corals ranged widely. There was an
average of 22 spp. per location on the shallow slopes of some reefs
in the Keppel region whereas there were more than 100 spp. in some
locations in the Whitsunday region. The overall average number of
species was 69.
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Densities of large coral colonies (definition of
“large” was species-specific) varied by a factor of
more than forty. Densities were lowest on the shallow slope of
Wentworth Reef (Cairns region) and the deeper slope on the front of
the Frankland Island (Innisfail region). The highest densities of
large colonies were found on shallow slopes of reefs at Cape
Tribulation (Cairns region) and Nelly Bay (Townsville region).
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Densities of small colonies (<10 cm maximum dimension,
density corrected for the area of suitable substrate) ranged from a
mean of less than one per square metre on the shallow reef slope on
the back of Keswick Island (Mackay region) to more than forty per
square metre in deeper parts of the reef slope of King Reef
(Innisfail region) and at the back of Dunk Island (Innisfail
region). The overall mean density was 15.6 small colonies per
square metre.
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Three broad community types were recognised: Acropora
dominated communities, Porites dominated communities and
mixed communities. Communities dominated by Acropora were
common in the Keppel region while Porites communities were
most common in the Innisfail region. Variation in community
structure was correlated with the grainsize of sediment at the
locations (an indicator of the resuspension/ deposition regime).
There was only a weak relationship with an estimate of risk of
exposure to runoff. The divergent communities in the Keppel and
Innisfail regions contributed substantially to both these
relationships.
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After correcting for differences in structure of coral
communities among regions, there were substantial differences in
community composition between shallow and deeper sites on reef
slopes. This difference was influenced by variation in either
settlement or early survival as the differences in abundance of a
number of coral genera between depths was due to variation in the
numbers of small colonies.
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Past studies giving information on status of near-shore reefs
are collated in an appendix. Examination of the few long-term data
sets on near-shore reefs showed that coral cover changed
dramatically in many of the sites. Most of the changes in
communities over time were due to changes in cover of Acroporidae
and, to a lesser extent, Pocilloporidae. Rates of recovery varied
widely, depending on the disturbance. After a cyclone, coral cover
on reefs at Cape Tribulation recovered quickly, increasing by more
than five percent a year, presumably through regrowth of damaged
colonies and the growth of fragments. In other instances, recovery
was minimal after several years, presumably because recovery
depended on recruitment of new individuals. It is clear that the
coral bleaching in 1998 had widespread and severe effects on coral
communities of near-shore reefs. Mortality associated with
bleaching has been partially responsible for the decline in
condition of some near-shore reefs in recent years. By killing
corals over a wide area, bleaching is also likely to have reduced
the regional supply of potential recruits on which recovery
depended. In 2004 many near-shore reefs had substantial densities
of small colonies that would have recruited after 1998. This
suggests that general recruitment failure, which is one of the
predicted results of excessive exposure to polluted runoff, was not
widespread.
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Surveys in 2004 provided a baseline for assessing future changes
in coral communities on near-shore reefs, but also raise many
questions about factors that determine the structure of the coral
communities, about their dynamics and their likelihood of
persistence in the long term. Accurate measurements of biophysical
variables at the survey sites, in combination with information on
disturbance history, could explain some of the fine-scale variation
in community structure. The few long-term data on coral communities
on near-shore reefs show strong effects of several kinds of
disturbance. For coral communities to persist they must recover
during intervals between disturbances. Rates of recovery will vary
with the kind of disturbance but there are few estimates of the
rates of recovery that can be expected under different conditions.
Recruitment of new colonies is essential for community resilience,
so the presence of numbers of small colonies of several genera in
many sites is a positive sign, but without information on survival
and growth rates under truly representative conditions it is
impossible to say whether even the highest densities of recruits
that were recorded will be sufficient to replace adults in the long
term. The Reef Water Quality Protection Plan provides an
opportunity to monitor near-shore reefs over several years so as to
relate community dynamics to local environmental conditions and to
disturbance in order to provide answers to these questions.
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