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International
Workshop Asia- Pacific Cooperation
Research for Conservation of Mangroves
26 -30 March, 2000; Okinawa, Japan
Below-ground
Carbon Sequestration of Mangrove Forests in the Asia-Pacific Region
Kiyoshi
Fujimoto
Forest
Environment Division, Forestry and Forest Products Research Institute,
Tsukuba
Abstract
The
belowground carbon storage and burial rate were examined for the
mangrove forests on Pohnpei Island in Micronesia, the southwestern
coast of Thailand, Iriomote Island in Japan and the Mekong Delta
in Vietnam. Stored carbon in a coral reef-type mangrove habitat
of Pohnpei Island consisting of a 2-m thick mangrove peat layer,
which is a type of mangrove habitat found in tropical Pacific islands,
was estimated to be 130 kg C m-2 (=1300 t C m-2).
In the southwestern coast of Thailand, stored carbon up to 1 m in
depth was estimated to be 50 kg C m-2 for R. apiculata
forest, 39 kg C m-2 for R. apiculata - Bruguiera
spp. or Xylocarpus spp. forest and 27 kg C m-2
for Ceriops tagal forest. In Iriomote Island, it was estimated
to be 50 kg C m-2 for Rhizophora stylosa forest.
In the Mekong Delta, it was estimated to be 33 kg C m-2
for R. apiculata forest on a flood deposit of ca. 100 years
ago and 27 kg C m-2 for a 20-year-old R. apiculata
plantation on the former Sonneratia - Avicennia habitat.
Carbon burial rates of these young forests were estimated to be
298 g C m-2 yr-1 during the last 100 years
and 580 g C m-2 yr-1 during the last 20 years,
respectively, which were faster than those estimated using the long-term
Rhizophora deposits formed during several hundred or several
thousand years, which were 25 to 93 g C m-2 yr-1.
Carbon burial rate of Rhizophora forest was faster than those
of other types of mangrove forest. These results suggest that Rhizophora
forest has higher belowground carbon sequestration ability than
other types of mangrove forest and displays its greatest ability
during the early stage of the forest.
Introduction
Mangrove
forests usually create thick, organically rich sediments as their
substrata. Most of the substrata in the tropics except under deltaic
environments consist of mangrove peat which mainly derives from
mangrove roots (Scholl, 1964ab; Woodroffe, 1981; Fujimoto &
Miyagi, 1993; Fujimoto et al., 1995b; Fujimoto et al.,
1996). This shows that mangrove forests have great belowground productivity
and play a significant role in carbon sequestration not only above
ground but also below ground.
There
have been many studies on aboveground biomass and productivity of
mangrove forests (e.g., Golley et al., 1962; Lugo
& Snedaker, 1974; Briggs, 1977; Christensen, 1978; Suzuki &
Tagawa, 1983; Tamai et al., 1986; Day et al., 1987;
Lee, 1990; Kusmana et al., 1992; Saintilan, 1997ab), but
few on the belowground biomass (Golley et al., 1962; Lugo
& Snedaker, 1974; Briggs, 1977; Komiyama et al., 1987;
Saintilan, 1997ab). Twilley et al. (1992) estimated the belowground
carbon storage based on restricted data about the belowground biomass,
excluding the sediments. This paper discusses carbon storage in
the sediments of various types of mangrove habitat in the Asia-Pacific
region and the burial rates using the data obtained from Pohnpei
Island in Micronesia (Fujimoto et al., 1999a), the southwestern
coast of the Malay Peninsula in Thailand, Iriomote Island in southwestern
Japan and the Mekong Delta in Vietnam.
Study
areas
Pohnpei
Island is situated in the humid tropics without a clear dry season
(lat. 6oo 45' to 7oo 00'N and long. 158oo 05' to 20' E) and mangrove
forests grow on the coral reef fringing the island though some of
them are situated in estuaries. The former is referred to as coral
reef type and the latter as estuary type. The typical mangrove habitat
of the coral reef type consists of a 2-m thick mangrove peat layer
(Fujimoto & Miyagi, 1993) and is usually covered by Rhizophora
apiculata dominant forest with Bruguiera gymnorrhiza,
Sonneratia alba and sometimes Xylocarpus granatum (Fujimoto
et al., 1995b, Kikuchi et al., 1999).
Field
research in Thailand was conducted in the Khlong Thom lowland (lat.
around 7oo 50' N and long. around 99oo 05' E) and the Satun lowland
(lat. around 6oo 35' N and long. around 100oo 05' E), which are
mainly situated in estuarine environments in the humid tropics with
a weak dry season. The mangrove forests in these areas were divided
into six communities, i.e. Sonneratia alba - Avicennia alba
community, Rhizophora apiculata community, R. apiculata
- Bruguiera spp. community, Ceriops tagal - Xylocarpus spp.
community, Lumnitzera littorea community and Excoecaria
agallocha community. These six communities distributed from
the middle part to the upper part of the tidal zone and corresponded
to the sediments (Mochida et al., 1999).
Iriomote
Island is situated in the subtropics (lat. 24oo 15' to 26' N and
long. 123oo 40' to 56' E) and the mangrove forests are valuable
as the most northerly in the world. Data for this study were collected
from the Rhizophora stylosa community and the B. gymnorrhiza
community on the small deltas at the mouth of the Nakama River and
the Shiira River, respectively.
Field
research in Vietnam was conducted at Tam Giang III in the Ca Mau
Peninsula, southern tip of the Mekong Delta (lat. around 8oo 50'
N and long. around 105oo 15' E) and the Can Gio Forest Park in eastern
Ho Chi Minh City (lat. around 10oo 25' N and long. around 106oo
52' E) in the humid tropics with a clear dry season. Data for this
study were collected from the R. apiculata pure forest converted
from the mixed forest with R. apiculata that developed about
50 years ago on the flood deposit of ca. 100 years ago at Tam Giang
III and the 20-year-old R. apiculata plantation on the former
Sonneratia ovata - Avicenia spp. habitat in Can Gio that
was destroyed by the herbicides and defoliants used by the United
States during the Vietnam war.
Methods
A
hand-operated, piston-type, thin-wall sampler 7.5 cm in diameter
was used for sampling non-disturbed cores, which cannot penetrate
coarse live roots and undecomposed large organic debris. Two-centimeter
thick samples for estimating carbon content were collected at intervals
of 10 to 30 cm. The remains were used for analyzing coarse organic
matter content. The coarse organic matter including live roots was
isolated by wet sieving using 0.5 mm meshed sieves. Total carbon
and nitrogen contents were analyzed using a CN corder (YANACO MT-600).
Samples collected in Vietnam were analyzed by the oxidation-reduction
titration method for carbon content in the laboratory of the Ho
Chi Minh City Agriculture & Rural Development Service.
Results
and discussion
Belowground
carbon storage
Table
1 shows the stored carbon in the four areas researched in the Asia-Pacific
region. The stored carbon in a coral reef-type mangrove habitat
covered by R. apiculata dominant forest consisting of a 2-m
thick mangrove peat layer in Pohnpei Island, which is a type of
mangrove habitat found in tropical Pacific islands, was estimated
at 130 kg C m-2 (=1300 t C ha-1) and that
in an estuary-type habitat reached around 200 kg C m-2
up to 3.5m in depth (Fujimoto et al., 1999a). In southwestern
Thailand, the stored carbon up to 1 m in depth in the R. apiculata,
R. apiculata - Bruguiera spp. or Xylocarpus spp.,
C. tagal forests were estimated to be about 50 kg C m-2,
39 kg C m-2 and 27 kg C m-2, respectively.
In Iriomote Island, it was estimated to be 50 kg C m-2
for the R. stylosa forest at the mouth of the Nakama River
and 22 kg C m-2 for the B. gymnorrhiza forest
at the mouth of the Shiira River. In the Mekong Delta, it was estimated
to be 33 kg C m-2 for the R. apiculata forest
on the flood deposit of ca. 100 years ago in the Ca Mau Peninsula
and 27 kg C m-2 for the 20-year-old R. apiculata
plantation on the former Sonneratia - Avicennia habitat in
Can Gio.
Table
1
Belowground
carbon storage of mangrove habitats in the
Asia-Pacific region
|
Habitat
type
|
Place
|
Forest
type
|
Sediments
|
No.
plots
|
Depth
(cm)
|
Stored
carbon (kg m-2)
|
Reference
|
|
Coral
reef
|
Pohnpei
Is., Micronesia
|
Ra
|
peat
|
3
|
200
|
130
|
Fujimoto
et al. (1999a)
|
|
Small
delta
or
estuary
|
South-western
Thailand
|
Ra
|
peat
|
2
|
100
|
50.16}1.88
|
unpublished
|
|
Ra-B
or X
|
organic
clay
|
4
|
100
|
39.00}5.67
|
ibid.
|
|
Ct
|
inorganic
clay
|
2
|
100
|
27.42}2.25
|
ibid.
|
|
Iriomote
Is.,
Japan
|
Rs
|
peaty
loam
|
3
|
100
|
49.71}6.96
|
ibid.
|
|
Bg
|
organic
loam
|
2
|
100
|
22.00}3.68
|
ibid.
|
|
Mega-delta
|
Ca
Mau,
Southern
Vietnam
|
Ra
on the flood deposit
of
ca. 100 years ago
|
clay
with peat
|
6
|
100
|
33.47}9.17
|
ibid.
|
|
Can
Gio,
Southern
Vietnam
|
20-year-old
Ra plantation
on
former So-A habitat
|
clay
|
3
|
100
|
27.05}3.51
|
ibid.
|
Ra:
Rhizophora apiculata, Rs: Rhizophora stylosa, Bg:
Bruguiera gymnorrhiza, B: Bruguiera spp., X: Xylocarpus
spp., Ct: Ceriops tagal, So: Sonneratia ovata, A:
Avicennia spp.
Carbon
burial rate
Table
2 shows the carbon burial rates of mangrove habitats in the Asia-Pacific
region. Fujimoto et al. (1999a) reported that the carbon
burial rates of the mangrove peat layer formed under the R. apiculata
dominant forest in Pohnpei Island were 55 g C m-2 yr-1
between 2620 and 1800 years BP in the falling sea-level phase, 93
g C m-2 yr-1 between 1800 and 1380 years BP
in the rising sea-level phase and 53 g C m-2 yr-1
during the last 1380 radiocarbon years in the stable sea-level phase.
These results suggest that Rhizophora forests display their
greatest belowground carbon sequestration ability during the rising
sea-level phase within the possible peat accumulation rate.
In
the southwestern coast of Thailand, relatively high carbon burial
rates were obtained from the R. apiculata - Bruguiera spp.
or Xylocarpus spp. communities, i.e. 70 g C m-2 yr-1
during the last 610 radiocarbon years and 105 g C m-2
yr-1 during the last 710 radiocarbon years, where sedimentation
rates, about 2 mm yr-1, were also relatively high (Fujimoto
et al. 1999b).
Table
2
Carbon
burial rates of mangrove habitats in the Asia-Pacific region
|
Place
|
Forest
type
|
Burial
period
(14C
years BP)
|
Stored
C
(kg
m-2)
|
C
burial rate
(g
m-2 yr-1)
|
Remarks
|
|
Pohnpei
Island1)
|
Ra
|
2620
to 1800
|
45.1
|
55
|
Falling
sea-level phase
|
|
Ra
|
1800
to 1380
|
39.0
|
93
|
Rising
sea-level phase
|
|
Ra
|
last
1380
|
75.0
|
53
|
Stable
sea-level phase
|
|
|
|
|
|
|
|
South-western
|
Ra-X
|
last
7102)
|
79.5
|
105
|
The
Khlong Thom lowland
|
|
Thailand
|
Ra-Bc
|
last
6102)
|
46.1
|
70
|
The
Satun lowland
|
|
Ra
|
last
13102)
|
43.9
|
32
|
The
Khlong Thom lowland
|
|
Ra
|
last
29202)
|
73.4
|
25
|
ibid.
|
|
Ct
|
last
16702)
|
23.8
|
14
|
The
Satun lowland
|
|
|
|
|
|
|
|
Iriomote
Island
|
Rs
|
last
10003)
|
49.7
|
50
|
The
Nakama River
|
|
Bg
|
last
10003)
|
22.0
|
22
|
The
Shiira River
|
|
|
|
|
|
|
|
South
Vietnam
|
Ra
|
last
1004)
|
29.8
|
298
|
On
the flood deposit
|
|
Ra
|
last
204)
|
11.6
|
580
|
20-year-old
plantation
|
1)
after Fujimoto
et al. (1999a), 2) using the radiocarbon ages
published by Fujimoto et al. (1999b), 3) general
period of mangrove habitat formation clarified by Fujimoto &
Ohnuki (1995), 4) calendar year. Ra: Rhizophora apiculata,
Rs: Rhizophora stylosa, Bc: Bruguiera cylindrica,
Bg: Bruguiera gymnorrhiza, Ct: Ceriops tagal, X: Xylocarpus
spp.
The
high sedimentation rate and high carbon burial rate seemed to have
been caused by the input of both inorganic and organic matters from
the upper stream. In the R. apiculata community, the carbon
burial rates were calculated at 25 g C m-2 yr-1
during the last 2920 radiocarbon years and 32 g C m-2
yr-1 during the last 1310 radiocarbon years. The lowest
value was obtained from the C. tagal community, which was
14 g C m-2 yr-1 during the last 1670 radiocarbon
years.
The
mangrove habitat on Iriomote Island usually has a 1-m thick mangrove
organic layer formed during the last 1000 years (Fujimoto &
Ohnuki, 1995). The carbon burial rates estimated using the general
period of formation and thickness of the mangrove organic layer
were about 50 g C m-2 yr-1 for the R. stylosa
forest at the mouth of the Nakama River and about 22 g C m-2
yr-1 for the B. gymnorrhiza forest at the mouth
of the Shiira River.
The
carbon burial rate of the R. apiculata forest in the Ca Mau
Peninsula developed on the flood deposit was estimated to be about
298 g C m-2 yr-1 during the last 100 years,
assuming that the carbon content of the lower part of the flood
deposit with few mangrove roots was the initial value of the flood
deposit. At Can Gio, the carbon burial rate during the last 20 years
after planting the R. apiculata was estimated to be 580 g
C m-2 yr-1, assuming that the carbon content
of the lower layer with few mangrove roots was the initial value
at the time of plantation.
These
results suggest that Rhizophora forest has higher carbon
sequestration ability than other types of mangrove forest and displays
its greatest belowground carbon sequestration ability during the
early stage of the forest.
References
Briggs,
S.V. (1977) Estimates of biomass in a temperate mangrove community.
Australian Journal of Ecology, 2, 369-373.
Christensen,
B. (1978) Biomass and primary production of Rhizophora apiculata
Bl. in a mangrove in Southern Thailand. Aquatic Botany,
4, 43-52.
Day,
J., Conner, W., Ley-Lou, F., Day, R. & Machado, A. (1987)
The productivity and composition of mangrove forests, Laguna
de Terminos, Mexico. Aquatic Botany, 27, 267-284.
Fujimoto,
K. & Miyagi, T. (1993) Development process of tidal-flat
type mangrove habitats and their zonation in the Pacific Ocean
: A geomorphological study. Vegetatio, 106, 137-146.
Fujimoto,
K. & Ohnuki, Y. (1995a) Developmental processes of mangrove
habitat related to relative sea-level changes at the mouth of
the Urauchi River, Iriomote Island, Southwestern Japan. Quarterly
Journal of Geography, 47, 1-12.
Fujimoto,
K., Tabuchi, R., Mori, T. & Murofushi, T. (1995b) Site environments
and stand structure of the mangrove forests on Pohnpei Island,
Micronesia. Japan Agriculture Research Quarterly,
29, 275-284.
Fujimoto,
K., Miyagi, T., Kikuchi, T. & Kawana, T. (1996) Mangrove
habitat formation and response to Holocene sea-level changes
on Kosrae Island, Micronesia. Mangroves and Salt Marshes,
1, 47-57.
Fujimoto,
K., et al (1999a) Below-ground carbon storage of Micronesian
mangrove forests. Ecological Res. 14, 409-413.
Fujimoto,
K., et al (1999b) Mangrove habitat dynamics and Holocene sea-level
changes in the southwestern coast of Thailand. TROPICS,
8, 239-255.
Golley,
F.B., Odum, H.T. & Wilson, A.F. (1962) The structure and
metabolism of a Puerto Rico mangrove forest in May. Ecology,
43, 9-19.
Kikuchi,
T., Mochida, Y., Miyagi, T., Fujimoto, K. and Tsuda S. (1999)
Mangrove forests supported peaty habitats on several islands
in the Northwestern Pacific. TROPICS, 8, 197-205.
Komiyama,
A., Ogino, K., Aksornkoae, S. & Sabhasri, S. (1987) Root
biomass of a mangrove forest in southern Thailand. 1. Estimation
by the trench method and the zonal structure of root biomass.
Journal of Tropical Ecology, 3, 97-108.
Kusmana,
C., Sabiham, S., Abe, K. & Watanabe, H. (1992) An estimation
of above ground tree biomass of a mangrove forest in East Sumatra,
Indonesia. TROPICS, 4, 243-257.
Lee,
S.Y. (1990) Primary productivity and particulate organic matter
flow in an estuarine mangrove wetland in Hong Kong. Marine
Biology, 106, 453-463.
Lugo,
A.E. & Snedaker, S.C. (1974) The ecology of mangroves. Annual
Review of Ecology and Systematics, 5, 39-65.
Mochida,
Y., Fujimoto, K., Miyagi, T., Ishihara, S., Murofushi, T., Kikuchi,
T. and Pramojanee, P. (1999) A phytosociological study of the
mangrove vegetation in the Malay Peninsula - special reference
to the micro-topography and mangrove deposit -. TROPICS,
8, 207-220.
Saintilan,
N. (1997a) Above- and below-ground biomass of two species of
mangrove on the Hawkesbury River estuary, New South Wales. Marine
and Freshwater Research, 48, 147-152.
Saintilan,
N. (1997b) Above- and below-ground biomass of mangroves in a
sub-tropical estuary. Marine and Freshwater Research,
48, 601-604.
Scholl,
D.W. (1964a) Recent sedimentary record in mangrove swamps and
rise in sea level over the southwestern coast of Florida: Part
1. Marine Geology, 1, 344-366.
Scholl,
D.W. (1964b) Recent sedimentary record in mangrove swamps and
rise in sea level over the southwestern coast of Florida: Part
2. Marine Geology, 2, 343-364.
Suzuki,
E. & Tagawa, H. (1983) Biomass of a mangrove forest and
a sedge marsh on Ishigaki Island, South Japan. Japanese Journal
of Ecology, 33, 231-234.
Tamai,
S., Nakasuga, T., Tabuchi, R. & Ogino, K. (1986) Standing
biomass of mangrove forests in Southern Thailand. Journal
of the Japanese Forestry Society, 68, 384-388.
Twilley,
R.R., Chen, R.H. & Hargis, T. (1992) Carbon sinks in mangrove
and their implications to carbon budget of tropical coastal
ecosystems. Water, Air, and Soil Pollution, 64,
265-288.
Woodroffe,
C.D. (1981) Mangrove swamp stratigraphy and Holocene transgression,
Grand Cayman Island, West Indies. Marine Geology, 41,
271-294.
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