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MESOPHOTIC CORAL ECOSYSTEMS – A LIFEBOAT FOR CORAL REEFS?

73

environments exposed to large temperature fluctuations on

daily or even hourly scales due to local-scale oceanographic

factors such as internal waves. In these cases, the local

oceanography could reduce the vulnerability of mesophotic

corals to bleaching both through mitigating maximum

temperatures and exposing corals to large fluctuations in

temperature to which they have become adapted (e.g. Buerger

et al. 2015). Water temperatures on MCEs may vary with

changes in the depth of the thermocline, particularly due to the

El Niño Southern Oscillation, upwelling and internal waves.

Thermocline depth appears to exert a significant influence on

MCEs, and a deepening of the thermocline associated with El

Niño events has been implicated in bleaching of corals in Palau

(Colin pers. obs.).

6.3.2.

Impact of highly variable temperature

regimes on mesophotic coral ecosystems

The El Niño Southern Oscillation is a naturally occurring

phenomenon that produces varying ocean temperatures

in the equatorial Pacific. It generally involves fluctuations

between two phases (El Niño and La Niña) that can last for

several seasons. For equatorial reefs in the Western Pacific,

El Niño events are associated with cool surface waters, and

shallow thermoclines and nutriclines. La Niña events cause

the opposite effect, with warm surface waters, and deep

thermoclines and nutriclines. This is in contrast to conditions

in the Central and Eastern Pacific, where warmer than normal

ocean temperatures are associated with El Niño and cooler

than normal temperatures are associated with La Niña events.

The oscillation between El Niño and La Niña conditions can

lead to rapidly fluctuating conditions that may pose a serious

threat to MCEs (Glynn and D’Croz 1990).

During a bleaching event in Palau in August 2010, constantly

high temperatures to a depth of 90 m were observed for periods

of hours to days (Figure 6.5). Overall, the 2010 bleaching event

was moderate and limited in duration, so coral mortality was low

(unlike the sustained bleaching event in 1998; Bruno et al. 2001).

6.3.3.

Disease

Disease in corals and other organisms has increased in

shallow coral reef ecosystems in the past decade along with

increasing seawater temperatures (Burge et al. 2014). Such

temperatures render organisms more susceptible to disease

outbreaks, as well as bleaching events. Recent surveys of

MCEs in Puerto Rico and the U.S. Virgin Islands indicate

that mesophotic coral communities are indeed susceptible

to biotic diseases (Smith et al. 2010, Weil unpubl. data — see

Puerto Rico Case Study in Chapter 3) down to at least 100 m

in depth. Coral bleaching and disease were observed in at

least six of the 23 mesophotic scleractinian coral species in

Puerto Rico (Figure 6.6) —

Agaricia undata

,

A. lamarcki

,

Undaria agaricites

,

Mycetophyllia aliciae

,

Montastraea

cavernosa

and

Stephanocoenia intersepta

. Most of the

“disease signs” observed fall into a general category known

as “white syndromes” due to their characteristic white area

of recent tissue-cleared skeletal material (Raymundo et al.

2008, Weil and Hooten 2008), with some signs resembling

typical white plague disease (Figure 6.6). In 2014 at Pulley

Ridge, an MCE in the eastern Gulf of Mexico, from a total

of 7,329 individual plate corals (

Agaricia

spp. and

Helioseris

cucullata

) counted from transect photos, 247 were noted to

be bleached, partially bleached, totally bleached, partly dead,

recently dead or diseased, resulting in 4 per cent morbidity

of the total population measured (Reed et al. 2015).

A good example of white plague disease-like signs was

observed in a single medium-sized (832 cm

2

) coral colony

of

Mycetophyllia aliciae

at 55 m off La Parguera, Puerto

Rico. This colony was healthy in October 2009, but showed

white plague disease-like signs in December 2009, and was

dead by March 2010 (Figure 6.7). Rate of tissue mortality

varied approximately between 6–10 cm/month, one-third

slower than the maximum tissue rate mortality reported

for this disease type in shallower waters, but still faster than

all other shallow coral diseases except black band disease

(Weil 2004).

Figure 6.7.

A time-series showing a colony of

Mycetophyllia aliciae

at 50 m off La Parguera, Puerto Rico that was (a) healthy in October

2009, (b) developed signs of white-plague-like disease and suffered rapid tissue mortality (white skeleton without tissue and secondary

macroalgae colonization) and (c) was dead by March of 2010 (photos Héctor Ruiz).

October 2009

December 2009

March 2010

October 2009

December 2009

March 2010

October 2009

Decemb r 2009

March 2010

(a)

(b)

(c)