Coral Reefs (2010) 29:361–367
DOI 10.1007/s00338-010-0596-3
REPORT
Mesophotic coral ecosystems in the Hawaiian Archipelago
J. Rooney • E. Donham • A. Montgomery
H. Spalding • F. Parrish • R. Boland •
D. Fenner • J. Gove • O. Vetter
•
Received: 30 March 2009 / Accepted: 2 February 2010 / Published online: 27 February 2010
Ó Springer-Verlag 2010
Abstract Efforts to map coral reef ecosystems in the
Hawaiian Archipelago using optical imagery have revealed
the presence of numerous scleractinian, zoothanthellate
coral reefs at depths of 30–130? m, most of which were
previously undiscovered. Such coral reefs and their associated communities have been recently defined as mesophotic
coral ecosystems (MCEs). Several types of MCEs are found
in Hawai‘i, each of which dominates a different depth range
and is characterized by a unique pattern of coral community
structure and colony morphology. Although MCEs are
documented near both ends of the archipelago and on many
of the islands in between, the maximum depth and prevalence of MCEs in Hawai‘i were found to decline with
Keywords Mesophotic coral ecosystem Hawai‘i
Main Hawaiian Islands Northwestern Hawaiian Islands
Coral morphology Coral distribution
Communicated by Guest Editor Dr. John Marr
Introduction
J. Rooney (&) E. Donham J. Gove O. Vetter
Pacific Islands Fisheries Science Center, Joint Institute
for Marine and Atmospheric Research, University Hawai‘i
and NOAA, NMFS, 1125-B Ala Moana Blvd., Honolulu,
HI 96814, USA
e-mail:
[email protected]
A. Montgomery
Division of Aquatic Resources, Department of Land
and Natural Resources, 1151 Punchbowl St.
Room 330, Honolulu, HI 96813, USA
H. Spalding
Botany Department, University of Hawai‘i Manoa,
3190 Maile Way, Honolulu, HI 96822, USA
F. Parrish R. Boland
Pacific Islands Fisheries Science Center, NOAA, NMFS,
2570 Dole St., Honolulu, HI 96822, USA
D. Fenner
Department of Marine and Wildlife Resources, PO Box 3730,
Pago Pago 96799, American Samoa
increasing latitude. The Main Hawaiian Islands (MHI) had
significantly deeper and greater percentages of scleractinian
coral, and peaks in cover of both scleractinian corals and
macroalgae occurred within depth bins 20 m deeper than in
the Northwestern Hawaiian Islands (NWHI). Across the
archipelago, as depth increased the combined percentage of
living cover of mega benthic taxa declined sharply with
increasing depth below 70 m, despite the widespread
availability of hard substrate.
Scleractinian coral reefs have been the subject of formal
scientific inquiry since at least 1842, when Darwin published his ‘‘Structure and Distribution of Coral Reefs’’.
However, the vast majority of research, monitoring, and
resource management has been focused on reefs and corals
within the depth range of traditional SCUBA diving. Little
attention has been focused on scleractinian coral reefs and
other associated benthic organisms below depths of ca.
30 m (Bak et al. 2005; Kahng and Maragos 2006; Kahng
and Kelley 2007; Menza et al. 2007). The term ‘‘mesophotic coral ecosystem’’ (MCE) has been designated to
describe light-dependant communities of corals and other
organisms found at these depths (Hinderstein 2010).
The scarcity of studies of MCEs relative to those
focused on shallow reefs is particularly acute in areas
outside the Caribbean region, including the insular Pacific
(Kahng et al. 2010). However, recent efforts to map coral
reef ecosystems (PIFSC 2008) have revealed the presence
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of a number of scleractinian zoothanthellate coral reefs at
depths of 30–130? m. This study characterizes the distribution and community structure of these MCEs and compares and contrasts those found in the Main Hawaiian
Islands (MHI) with those found in The Main Hawaiian
Islands (MHI). The results are based on an analysis of more
than 400 linear kilometers of seafloor video imagery collected at 19 islands, banks, and atolls within the Hawaiian
Archipelago, supplemented by data collected during submersible and technical SCUBA dives.
Materials and methods
Data collection
Most of the data discussed here are seafloor videos, plus a
limited number of still photographs, collected by several
different underwater camera sleds (PIFSC 2008). Additional
imagery and a limited number of coral samples were collected in the Au‘au Channel between the islands of Maui and
Lāna‘i using Pisces submersibles and a RCV-150 remotely
operated vehicle (ROV) operated by the Hawai‘i Undersea
Research Laboratory (HURL). Direct observations in the
Main Hawaiian Islands (MHI) were also made during
HURL submersible dives and technical SCUBA dives.
Coral samples were identified using published guides
(Veron 2000; Fenner 2005), and identification was confirmed by invertebrate taxonomists at the Bishop Museum.
The camera sleds have all utilized a stainless steel frame
approximately 1 9 0.6 9 0.6 m in size and have been
deployed from small boats and NOAA ships to depths of
approximately 150 m. They have been equipped with a
color video camera including a Deep Sea Power and Light
(DSP&L) Multi SeaCam 2050 or 2060, or a Remote Ocean
Systems model MC055HR. These cameras had resolutions
of 460 (H) 9 400 (V) pixels for the Multi SeaCam 2050,
and 768 (H) 9 494 (V) pixels for the other two. The video
feed from a sled was sent via an umbilical cable to a video
monitor in the topside control unit, which an operator
watched to adjust the altitude of the sled to keep it 1–3 m
above the seafloor. The towing vessel drifted at speeds of
approximately 0.8 m s-1 (1.6 knots) or less. Camera sleds
were also equipped with two 500 W or 250 W DSP&L
Multi-SeaLite underwater lights, a depth sensor, a sonar
altimeter, and a set of parallel scaling lasers.
Primary cameras on the Pisces submersibles were Sony
3-chip PDX-10 digital video cameras with two 400 W
DSP&L HMI lights. Submersible pilots also used an
Olympus SP-550UZ camera with 7.1 megapixel resolution
to shoot still images through the viewports. The RCV-150
had a color analog video camera, two parallel lasers for
scale, and six 250 W lamps.
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Coral Reefs (2010) 29:361–367
Data processing
Video data from camera sleds and ROV dives were classified at 5 points spaced equidistantly in a horizontal line
across the monitor screen, at 30 s intervals, with a mean
distance between intervals of 10.3 m ±3.7 (mean ± SD).
Substrate type, living cover (scleractinian coral, crustose
coralline algae, macroalgae, non-scleractinian corals), and
other benthic characteristics were recorded in the classification process. The non-scleractinian corals category
includes black and soft corals, sea fans, sea whips, etc. A
small percentage of living cover (2.8%) was labeled as
unclassified when it was not possible to distinguish
between different types of benthic organisms. Substrates
types were classified as either hard (solid rock, boulders,
rubble) or soft (sand, mud). All classification points fell
into one of these categories, except for a small subset
(0.96%), labeled as ‘‘unclassified,’’ for which the substrate
type could not be identified. Unclassified points were
excluded from further analyses.
Methodological limitations
Video cameras on the camera sleds typically produce
imagery that is not of sufficient resolution to identify corals
or other organisms to species level. Frame grabs extracted
from the videos yield a still image less than 0.4 megapixels
in size. The image quality is further degraded by the video
interlacing process, which gives them half the resolution of
the source video. To minimize loss of resolution and enable
video analysts to see objects at different angles as they
move through the camera’s field of view, analysis was done
using the video itself rather than on frame grabs. The speed
of the camera sled, especially when it was very close to the
seafloor, was occasionally too fast to allow the camera to
fully focus. Turbid water conditions, insufficient lighting,
and excessively high camera altitudes also occasionally
degraded image quality. Less visually obvious organisms
were hard to distinguish and are probably underrepresented.
Most often deployed from large research ships with
limited maneuverability, the camera sleds have collected
optical data with positional uncertainties that range
between ca. ±15 to ±100 m. Data collection is often
precluded on windward sides of islands, off coastlines with
steep nearshore bathymetry, and other areas where it is
unsafe for large vessels to operate. Imagery from the sleds
is effective for identifying features such as mesophotic
reefs at spatial scales from several tens of meters to a few
kilometers, but rare organisms are under-represented, or
missed altogether. These scales are adequate for identifying broad distribution patterns, for supporting some
spatially based resource management actions, and for the
Coral Reefs (2010) 29:361–367
363
identification of sites for more localized and detailed
studies requiring other methods.
Results
A total of 334 seafloor videos and 3,733 still photographs
collected by underwater camera sled and ROV dives,
covering 407 linear km of seafloor, were analyzed and
mapped (Table 1). Still and video imagery and direct
observations from 18 submersible dives in the Au‘au
Channel and several dozen technical SCUBA dives at
several of the MHI were used to collect samples and to help
develop a better understanding of MCEs.
Imagery was collected around 6 of the 8 islands in the
MHI, but 76% of the data are from the Au‘au Channel.
Likewise in the NWHI, a majority of the data came from a
single location, French Frigate Shoals, with 56% of the
imagery. Percentages of the seafloor composed of different
substrates and colonized by different types of benthic
organisms were recorded from seafloor imagery collected
in the MHI (Fig. 1a) and NWHI (Fig. 1b) and binned by
depth interval.
Discussion
Mesophotic corals have been found from near the southern
end of the Hawaiian Archipelago off the southwestern
corner of the island of Maui to the northern end, off Kure
Atoll (Fig. 2). Thus, all Hawaiian Islands and atolls appear
to have the potential to host MCEs. The level of survey
effort at different islands has not been evenly distributed
either geographically or vertically, and most islands need
significantly more data collected before their distribution,
Table 1 Optical data collection statistics and coral reef ecosystem
areas
MHI
NWHI
Seafloor transect total length (km)
154
Number of videos
108
226
334
0
3,733
3,733
Shallow coral ecosystem area
(km2 \ 30 m depths)
1,538
6,241
7,779
Mesophotic ecosystem area
(km2 30–100 m depths)
7,987
4,396
12,383
Number of still photos
253
Total
407
The size of the shallow coral reef ecosystem, calculated as the area of
seafloor between the 0- and 30-m isobaths, shown for the different
parts of the archipelago discussed in this study. Although they often
extend deeper, the total size of MCE habitat in Hawai‘i is conservatively calculated as the area of seafloor between the 30-m and
100-m isobaths
and other characteristics of MCEs can be definitively
described. However, the existing data suggest that several
types of MCEs are found in the Hawaiian Archipelago.
Each type dominates a different depth range, is characterized by a unique pattern of coral community structure and
coral colony morphology (Fig. 3), and is hypothesized to
be controlled by a suite of physical factors unique to that
type.
Upper mesophotic MCEs
Upper Mesophotic MCEs are found at depths from ca. 30–
50 m. They are often found off coastlines exposed to
winter season long period swell and appear to be sheltered
by depth from the damage due to seasonal high wave
events that preclude coral reef accretion at shallower
depths (Dollar 1982; Dollar and Tribble 1993; Fletcher and
Sherman 1995; Grigg 1998; Rooney et al. 2004). Conditions including relatively clear water in summer months
and higher than average current velocities during the winter
are hypothesized to provide optimal conditions for coral
reefs in this zone. Upper Mesophotic MCEs are dominated
by a few of the coral species found in shallow reefs
including Pocillopora meandrina, P. damicornis, Montipora capitata, and Porites lobata. Other species including
Leptastrea purpurea, Leptoseris hawaiiensis, L. mycetoseroides, Pocillopora eydouxi, and Porites compressa have
also been occasionally observed. High densities of a species of Pocillopora (probably P. meandrina) are found in
the Upper Mesophotic as far north as Kure Atoll. In the
NWHI, large numbers of rare species of fish, such as
the Hawaiian Morwong, Cheilodactylus vittatus, and the
Masked Angelfish, Genicanthus personatus, are seen in
abundance on Upper Mesophotic MCEs. Thick mats of the
green alga Microdictyon setchellienum and a brown alga
(Dictyopteris sp. or Sargassum sp.) are also common there
(Parrish and Boland 2004).
Branching/plate coral MCEs
Branching/Plate Coral MCEs are typically found at depths
between ca. 50–80 m. Some of these reefs were dominated
by thick stands of low-relief branching corals that may
stand as high as ca. 30 cm (Fig. 4a). A few samples of
these corals have been tentatively identified as a species of
Montipora or Anacropora. Work is on-going, including
both skeletal structure and genetic analyses to positively
identify this species (S. Coles, pers. comm.). Other reefs in
this depth range were dominated by Montipora capitata
with a plate-like morphology (Fig. 4b). Colonies of Leptoseris species including: L. hawaiiensis, L. incrustans,
L. mycetoseroides, L. papyracea, and L. tubulifera were
occasionally encountered, particularly near the deeper end
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Coral Reefs (2010) 29:361–367
b
a
80%
a
80%
60%
60%
40%
40%
20%
20%
30-40
60-70
30-40
60-70
De
De
90-100
pt
h
(m
)
90-100
pt
120-130
h
120-130
(m
)
150-160
150-160
170+
170+
Scleractinian Coral
Macroalgae
Non-scleractinian Coral
Hard Substrate
Coralline Algae
Sand Substrate
Fig. 1 The percent cover (shown on the vertical axis) of substrate type, scleractinian corals, and other megabenthic taxa from mesophotic depths
binned into 10-m depth intervals, for: a Main Hawaiian Islands, b Northwestern Hawaiian Islands
170°W
165°W
160°W
155°W
20.8
- Branching/Plate Coral MCEs
Pearl and
Hermes
Atoll
- Leptoseris MCEs
19.9
Midway
Atoll 14.6
27.3
Lisianski
Island
- No MCEs
Pioneer
Bank
26 - km of seafloor imagery
Maro
Reef
Laysan
Island
5.0
Brooks
Banks
25°N
Kure
At ll
30°N
Legend
- Upper Mesophotic MCEs
Necker
Island
6.9
Gardner
Pinnacles
French Frigate
Shoals 144.2
13.2
Twin Nihoa
Banks
5.3 Moloka‘i
Maui
13.4
117.0
O‘ahu
20°N
4.7
20°N
30°N
175°W
25°N
Fig. 2 Known mesophotic
coral ecosystems (MCEs) in the
Hawaiian Islands. Locations of
different types of MCEs are
shown with color coded stars.
Areas where imagery from
multiple camera sled
deployments has been collected
and no MCEs have been found
are shown within the green
circles
Kaho‘olawe
15°N
Kilometers
0
175°W
of this depth range and were often interspersed with
branching corals. It has been demonstrated that Montipora
capitata is able to meet all of its metabolic energy
requirements through heterotrotropic feeding (Grottoli
et al. 2006), and optimal conditions for these reefs are
hypothesized to include direct exposure to strong currents
with high concentrations of zooplankton.
123
170°W
165°W
200
400
160°W
600
800
1,000
15°N
Hawai‘i
("Big Island")
155°W
Leptoseris coral MCEs
Leptoseris coral MCEs were the dominant reef type found
at depths from ca. 80 m to at least 130 m (Fig. 4c). In the
Hawaiian Archipelago, Leptoseris MCEs are dominated by
large thin-walled colonies with plate-like to foliaceous
morphologies. Believed to be a compromise between
Percentage of Total
Coral Cover
Coral Reefs (2010) 29:361–367
365
100
80
Massive
Plate-like
Encrusting
Branching
60
40
20
0
0
12
011
00
-1
90
0
-8
70
0
-6
50
0
-4
30
Depth Bins (m)
Fig. 3 Mean percentages of coral colony morphologies versus depth.
Vertical red-dashed lines indicate divisions between different types of
MCEs, based on morphological considerations
optimal light interception and reduced skeletal carbonate
deposition (Fricke et al. 1987), they create a myriad of
small crevices and holes on the seafloor. Species richness
of some fishes has been found to correlate strongly with
live coral cover, while the abundance of other fish species
is thought to be enhanced by habitat with crevices and
escarpments (Colin 1974). Thus, it is hypothesized that
Leptoseris MCEs, in particular, provide desirable habitat
for some fish species. The most common coral species
observed was Leptoseris hawaiiensis, but colonies of
L. papyracea, L. scabra, L. tubulifera, and L. yabei have
also been found. No shallow water coral species were
observed on Leptoseris coral MCEs and, consistent with
other studies (Goreau and Goreau 1973; Reaka et al. 2010),
they appear to have the lowest species diversity of the
different types of MCEs discussed in this study.
Vertical zonation
Scleractinian coral cover at mesophotic depths in the MHI
(Fig. 1a) peaked between depths of 50–60 m with a value
of 22% and gradually declined with increasing depth.
Macroalgal cover peaked deeper (60–70 m) at a value of
36% before declining to near zero below 130 m. Nonscleractinian coral remained at low levels at all mesophotic
depths in both the MHI and NWHI. Data density is quite
low below 140 m in the MHI and covers less than 200 m of
seafloor. Thus, the high percentages of coralline algae
recorded below 140 m (Fig. 1a) must be considered to be
more representative of the limited areas where data were
collected than of the entire MHI at those depths.
Vertical distribution patterns for benthic communities in
the NWHI (Fig. 1b) were markedly different than those
from the MHI. Mean scleractinian coral cover peaked at
17% in the 30–40 m depth bin and declined to near zero
below 50 m. Peak abundance of macroalgae was found at
Fig. 4 Types of mesophotic coral ecosystems found in the Hawaiian
Archipelago, including: a Branching coral MCE found off Kauai, at a
depth of 56 m. The coral colonies on the left-hand side of the image
are approximately 10 cm in diameter. Photograph credit: Jason
Leonard. b Plate coral MCE, dominated by colonies of Montipora
capitata, at a depth of 55 m off Oahu. Photo credit: Tony
Montgomery. c Leptoseris MCE, dominated by colonies of Leptoseris
hawaiiensis, at a depth of 90 m in the Au‘au Channel off Maui. Note
the cluster of fish in the background. Photo credit: Hawai‘i Undersea
Research Laboratory
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Coral Reefs (2010) 29:361–367
Archipelago-wide observations
70
% Hard Substrate
% Total Live Cover
50
40
30
20
10
0
15
13
0-
0-
16
14
12
00
0-
-1
0
0
0
Fig. 5 Total percentages of living cover of megabenthic taxa
(scleractinian and non-scleractinian corals, macroalgae, and crustose
coralline algae), and hard substrate, plotted against depth, for the
Hawaiian Archipelago
43% in the 40–50 m depth range and then declined more
rapidly than in the MHI. Coralline algae peaked at 8% in
the 30–40 m depths and declined gradually.
Peaks in cover of both scleractinian corals and macroalgae occurred within depth bins 20 m shallower in the
NWHI than in the MHI. Overall, the MHI had markedly
deeper and greater percentages of scleractinian coral.
Within the archipelago as a whole, the total mean percentage of all types of living cover hovered between 40 and
50% between depths of 30–70 m and then abruptly
declined to levels slightly above 10% at depths of 90 m
(Fig. 5). The percentage of hard substrate uncolonized by
megabenthic taxa hovered between 0 and 20% between
depths of 30–100 m. Consistent with other studies (Lang
1974; Avery and Liddell 1997; Kahng and Kelley 2007),
the uncolonized percentage then jumped to an average of
25% below 100 m, suggesting that competitive exclusion
has less influence on community structure and diversity at
deeper depths throughout the archipelago.
September 2006
20
19
−250
18
17
16
18
17
18
17
16
16
16
15
20
19
21
20
19
18
17
20
15
16
18
16
16
16
14
15
14
15
14
es
erm
dH
an
arl
Pe
ski
ian
Lis n
ysa
La
ro
Ma
r
ne
rdi
Ga
ate
rig
hF
nc
Fre
r
cke
Ne
re
Ku
es
ay Herm
dw
Mi and
arl
Pe
ski
ian
Lis n
ysa
La
ro
Ma
oa
Nih
ate
rig
hF
nc
Fre
r
cke
Ne
−300
22
17
18
19
18
17
16
18
20
14
15
26
24
22
18
21
21
−200
22
21
20
19
21
20
19
22
−150
26
25
24
23
Temperature (°C)
23
22
23
22
27
22
26
25
24
−100
Depth (m)
26
25
24
19
28
27
−50
15
123
March 2005
23
Fig. 6 Typical thermal
structure of the upper water
column of the Northwestern
Hawaiian Islands during near
peak winter and summer
seasonal conditions
21
0
0
0
-6
-4
-8
11
90
70
50
30
Depth Bins (m)
Growth rates of shallow water corals in fore reef zones
across the Hawaiian Archipelago decrease linearly with
increasing latitude due to reduced sea surface temperatures
and light (Grigg 1981; Siciliano 2005). Likewise, MCEs
were found to be generally better developed and found at
deeper depths closer to the southern end of the archipelago.
Isotherms become shallower moving to the northwest along
the Hawaiian Ridge (Fig. 6), particularly during the winter
season, and are likely to limit reef growth at deeper depths
(Grigg 1981). The annual range in seawater temperature at
mesophotic depths becomes larger toward the northern end
of the NWHI and is hypothesized to be another factor
inhibiting reef growth.
This study documents the presence of MCEs on many
islands and near both ends of the Hawaiian Archipelago,
suggesting that the potential exists for many, if not most,
islands to host them. Although individual MCEs have been
found to have high densities and cover of scleractinian
corals, mean cover at island or archipelago scales is generally low, reflecting the patchy distribution of MCEs.
Moreover, the potential habitat for MCEs in the Hawaiian
Islands, conservatively estimated as the area of seafloor
between the 30- and 100-m isobaths, is quite large.
Encompassing 13,180 km2, it is 62% larger than the
potential habitat of shallow reefs, or the area of seafloor
between the shoreline and the 30-m isobath (Table 1).
These factors and the challenges of working at mesophotic
depths (e.g., Menza et al. 2007) have prevented the discovery of many of the MCEs analyzed here until recently
and suggest that additional surveying is likely to discover
new MCEs. In addition, information regarding the species
composition of MCEs, their ecological roles in wider coral
reef ecosystems, how these change along gradients of depth
and latitude, and many other questions remain unanswered.
17
Percent Cover
60
Coral Reefs (2010) 29:361–367
Effective ecosystem-based management requires that all
of the significant components of the ecosystem be explicitly considered and included in management efforts. Programs that ignore the mesophotic realm are systematically
neglecting a major component, at least in Hawai‘i, of the
overall coral reef ecosystem. Given the collective magnitude of threats facing coral reefs today (e.g., Jackson et al.
2001; Hughes et al. 2003; Pandolfi et al. 2005; HoeghGuldberg et al. 2007; Stone 2007), it is important to
improve our understanding of MCEs and to explicitly
include them in studies, monitoring programs, and management strategies.
Acknowledgments This research was made possible by grants from
the National Oceanic and Atmospheric Administration (NOAA) Coral
Reef Conservation Program to the Coral Reef Ecosystem Division of
the NOAA Pacific Islands Fisheries Science Center. Additional support was provided by the NOAA Coastal Ocean Program to the
NOAA Pacific Islands Fisheries Science Center. Submersible support
was provided by NOAA Undersea Research Program’s Hawai‘i
Undersea Research Laboratory under award NA05OAR4301108. The
assistance of Scott Ferguson, Rusty Brainard and the staff of the Coral
Reef Ecosystem Division and the officers and crew of the NOAA
ships O.E. Sette and Hi‘ialakai are gratefully acknowledged. Steve
Coles of Bishop Museum provided taxonomic identification of coral
samples. Frances Lichowski assisted with the preparation of Figures.
Several anonymous reviewers made numerous suggestions to improve
this manuscript.
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