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Jackson2013-Status and Trendsof Caribbean Coral Reefs

Jackson2013-Status and Trendsof Caribbean Coral Reefs.pdf

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2b. ECOLOGICAL EXTINCTION OF<br />

FORMERLY DOMINANT SPECIES<br />

Three taxa of formerly very great ecological<br />

significance on <strong>Caribbean</strong> reefs suffered<br />

massive declines up to several decades<br />

before the first quantitative surveys at the<br />

vast majority of the 90 locations in Table<br />

2. Underst<strong>and</strong>ing the subsequent decline<br />

of <strong>Caribbean</strong> reefs hinges upon a clear<br />

underst<strong>and</strong>ing of the magnitude of these<br />

early changes that in most places have hardly<br />

left a trace.<br />

Decline of Acropora palmata <strong>and</strong> A. cervicornis<br />

Acropora palmata <strong>and</strong> A. cervicornis were<br />

among the most abundant <strong>and</strong> ecologically<br />

dominant corals on <strong>Caribbean</strong> reefs in depths<br />

down to 20 m for the last one million years<br />

until the 1970s <strong>and</strong> 1980s (Goreau 1959;<br />

Geister 1977; Lewis 1984; Jackson 1992,<br />

1994; Aronson <strong>and</strong> Precht 2001; P<strong>and</strong>olfi<br />

<strong>and</strong> Jackson 2006; Johnson et al. 2008).<br />

Both species experienced intense mortality<br />

due to White B<strong>and</strong> Disease (WBD) since<br />

the mid to late 1970s until today (Gladfelter<br />

1982; Porter <strong>and</strong> Meier 1992, Aronson <strong>and</strong><br />

Precht 2001, Porter et al. 2001, Patterson et<br />

al. 2002, Weil <strong>and</strong> Rogers 2011). Hurricanes<br />

<strong>and</strong> outbreaks of predators also devastated<br />

acroporids in Jamaica <strong>and</strong> the USVI in the<br />

1980s (Knowlton et al. 1981, 1990; Woodley<br />

et al. 1981; Rogers et al. 1991; Rogers <strong>and</strong><br />

Miller 2006), <strong>and</strong> there is paleontological<br />

evidence for die-offs several decades earlier<br />

in Barbados (Lewis 1984), Bocas del Toro<br />

Panama (Cramer et al. 2012), <strong>and</strong> more<br />

broadly throughout the region (Jackson et al.<br />

2001).<br />

Unfortunately there are remarkably few<br />

quantitative data on the abundance of<br />

either species until they were already greatly<br />

diminished by disease, a spate of hurricanes<br />

in close succession, <strong>and</strong> degrading water<br />

quality to be reviewed in the next section.<br />

To address this, we compiled a very large<br />

qualitative database on the occurrences of<br />

both species back into the 19 th century to<br />

supplement the quantitative data (Appendix<br />

3). The proportion of reef sites with presence<br />

<strong>and</strong> dominance of Acropora palmata <strong>and</strong> A.<br />

cervicornis was computed for the time period<br />

from 1851-2012. Data include qualitative<br />

<strong>and</strong> quantitative information from the primary<br />

peer-reviewed scientific literature, government<br />

reports, <strong>and</strong> less commonly historical<br />

literature as well as quantitative data received<br />

directly from contributors to this study <strong>and</strong><br />

compiled in the larger GCRMN database.<br />

Quantitative data include percent cover for<br />

either Acropora species, while qualitative<br />

data include presence/absence <strong>and</strong> relative<br />

abundance data, as well as descriptions of<br />

relative abundance categories (Appendix<br />

3). Data are primarily from underwater field<br />

surveys, although a small number are from<br />

boat-based observations <strong>and</strong> high-resolution<br />

aerial photographs. Data from the literature<br />

were extracted from texts, tables, figures, <strong>and</strong><br />

maps.<br />

Only data from “reef crest” <strong>and</strong> “midslope”<br />

reef zones were included in the analysis.<br />

Generally, reef crest data spanned 0-6m<br />

water depth <strong>and</strong> midslope data spanned<br />

between 6-20m, as 6m was the depth at<br />

which dominance typically shifted from A.<br />

palmata to A. cervicornis in the quantitative<br />

data. However, the distinction between reef<br />

crest <strong>and</strong> midslope was made on a reef siteby-site<br />

basis, taking into account additional<br />

information on reef zone or reef morphology,<br />

if available. For some locations, the cutoff<br />

was closer to 10m, the same value used in<br />

Jackson et al. (2001). Data were not included<br />

if determination of the reef zone could not be<br />

made. Data were recorded at the reef site level<br />

<strong>and</strong> computed by averaging over replicates<br />

within the same reef site <strong>and</strong> reef zone. In<br />

total, 1,863 reef sites from 79 locations were<br />

compiled for the reef crest zone <strong>and</strong> 4,569<br />

reef sites from 83 locations for the midslope<br />

zone. These included locations that were not<br />

represented in the master GCRMN quantitative<br />

database (Table 2).<br />

Results are presented in Figs. 20 <strong>and</strong> 21 for<br />

A. palmata <strong>and</strong> A. cervicornis respectively.<br />

Sample size is small before 1950, <strong>and</strong> the<br />

locations represented in various time bins are<br />

not consistent. Nevertheless, the data confirm<br />

the remarkably great abundance of both<br />

species before the 1970s. Acropora palmata<br />

was present at more than 80% of all areas<br />

surveyed in depths less than 10 m throughout<br />

the wider <strong>Caribbean</strong> region <strong>and</strong> was recorded<br />

as “dominant” at 60% of these localities.<br />

42 STATUS AND TRENDS OF CARIBBEAN CORAL REEFS: 1969-2012

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