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CORDIO Status Report 2000

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Figure 2. Three strategies for bleaching and mortality obtained from<br />

cluster analysis of 17 species of corals, showing tendency for normal,<br />

pale, bleached or dead condition during, 6 months after, and 1 year after<br />

the El Niño. Membership in the groups is: Group A - Acropora eurystoma,<br />

Galaxea astreata, Pocillopora damicornis, Porites nigrescens, Pocillopora<br />

verrucosa. Group B: Favites pentagona, Favia favus, Galaxea fascicularis,<br />

Platygyra daedelea, Porites lutea, Echinopora gemmifera, Hydnophora exesa.<br />

Group C: Favia pallida, Pavona varians, Sinularia spp., Montipora informis,<br />

Montipora tuberculosa. Source. Obura (<strong>2000</strong>).<br />

100<br />

75<br />

Normal<br />

Pale<br />

Relative abundance (%)<br />

20<br />

15<br />

10<br />

5<br />

Nov-99 (n=194) (n=194)<br />

Mar-99 Mar-00 (n=194) (n=251)<br />

Percent<br />

50<br />

Bleached<br />

0<br />

25<br />

0<br />

0 6 12<br />

Months<br />

Dead<br />

group C. The divisions among the groups are somewhat<br />

consistent with differences in coral species resistance to<br />

other stresses, such as sedimentation (Obura, 1995) and<br />

in studies of coral life history strategies (Hughes & Jackson,<br />

1985; Kojis & Quinn, 1991). These patterns offer<br />

hypotheses for attempts to understand the ecological<br />

and evolutionary effects of El Niño-related and other<br />

stresses on the long-term prospects for coral reef survival.<br />

It also offers the possibility of using a suite of species<br />

with known responses as indicators for reef status either<br />

through observation of natural corals, as analysed here,<br />

or observation of transplants as bioassays (Obura, <strong>2000</strong>;<br />

this volume).<br />

Coral recruitment in 1999 was low at almost all sites<br />

surveyed, with few or no recruits less than 2 cm to 3 cm<br />

in diameter seen at most reefs (Obura, personal observation).<br />

One exception is an extremely shallow back reef<br />

coral area at Kanamai, approximately 20 km north of<br />

Mombasa, where recruitment of Poillopora damicornis,<br />

one of the species that ‘disappeared’ for more than a<br />

year following the El Niño, and other opportunistic species<br />

such as Porites nigrescens and Pavona spp. was high.<br />

5<br />

15<br />

25<br />

35<br />

45<br />

55<br />

65<br />

75<br />

85<br />

95<br />

105<br />

115<br />

125<br />

135<br />

145<br />

155<br />

165<br />

175<br />

185<br />

195<br />

500<br />

Size classes, upper boundary (mm)<br />

Figure 3. Pocillopora damicornis size class structure, Kanamai, November<br />

1999 and March <strong>2000</strong>. The number of colonies sampled is shown<br />

in brackets.<br />

The population of P. damicornis at this site was sampled<br />

in November 1999 and March <strong>2000</strong> (Figure 3) and<br />

showed a higher peak of smaller classes in November<br />

suggestive of recruitment since the El Niño. While this<br />

species suffered 100% mortality at all reefs surveyed,<br />

there is clearly a source population somewhere that<br />

seeded the Kanamai reef. The size and distribution of<br />

these remnant populations is likely to have a great impact<br />

on the recovery of coral communities throughout<br />

Kenya.<br />

ZOOXANTHELLAE AND CHLOROPHYLL IN<br />

CORALS<br />

Research on zooxanthellae and chlorophyll concentrations<br />

in Kenyan corals started in late 1997 just prior to<br />

the El Niño (Mdodo, 1999; Mdodo & Obura, 1999), and<br />

sampling has continued almost continuously since then.<br />

Five coral species were selected for monitoring (Figure<br />

4), with ‘normal’ zooxanthellae and chlorophyll concentrations<br />

of 1-5 million/cm 2 and 1.5-8.0 µg/cm 2 respec-<br />

– 29 –

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