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J. Bio. Env. Sci. 2016
265 | Barcelete Jr et al.
RESEARCH PAPER OPEN ACCESS
Species diversity and above-ground carbon stock assessments in
selected mangrove forests of Malapatan and Glan, Sarangani
Province, Philippines
Ricky C. Barcelete Jr*
, Eva Mae F. Palmero1
, Bhegie May G. Buay1
, Cyril B. Apares1
,
Lanny R. Dominoto1
, Harold Lipae1
, Ma. Luisa N. Cabrera1
, Mark Anthony J. Torres2
,
Elani A. Requieron1
1
Science Department, Mindanao State University, General Santos, Philippines
2
Department of Biological Sciences, Mindanao State University, Iligan, Philippines
Article published on February 28, 2016
Key words: Sonneratia alba, Rhizophora apiculata, C-stocks.
Abstract
Mangrove ecosystems are known for being the rainforest of the sea. Philippines is bestowed with this naturally
rich mangrove ecosystem with diverse floral and faunal species. Despite this natural abundance, mangrove
ecosystems are subjected to natural and human induced degradations specifically conversion to fish shrimp
ponds that resulted in diminution aside from its effect on terrestrial and oceanic carbon cycling and could also
affect its important role in terms of terrestrial and oceanic carbon cycling. This study is conducted to determine
the mangrove diversity, distribution and the above-ground biomass and C-stocks in Glan and Malapatan,
Sarangani Province. Purposive sampling is implemented in establishing the plots on both sites. Results show
eight (8) mangrove species belonging to four (4) families are observed in both areas. Data also reveal that the
mangrove ecosystem in Glan Padidu, Glan is undisturbed. Rhizophora apiculata and Sonneratia alba are found
to be dominant on the two sites. Because of the large tree girths and high density of species observed on the
studied areas, both forests have the potential to sequester and store large amount of atmospheric carbon. Thus,
this study quantifies mangrove tree biomass in view of carbon trading as significant in lessening the effects of
global warming.
*Corresponding Author: Ricky C. Barcelete Jr.  ricky_barcelete@yahoo.com
Journal of Biodiversity and Environmental Sciences (JBES)
ISSN: 2220-6663 (Print) 2222-3045 (Online)
Vol. 8, No. 2, p. 265-274, 2016
http://www.innspub.net
J. Bio. Env. Sci. 2016
266 | Barcelete Jr et al.
Introduction
Mangrove forest is also known as the “rainforest of
the sea”. It grows well on mudflats and banks of
tropical and subtropical rivers and coastlines, existing
at the boundary of land and water and receiving
nutrients from both environments (Ramos, 2013).
Mangroves are salt tolerant trees (halophytes)
because they contain a complex salt filtration system
and complex root system to cope with salt water
immersion and wave action. They are also anoxic,
adapted to the low oxygen conditions of waterlogged
mud. They have these highly developed
morphological, biological, ecological and
physiological adaptations to extreme conditions that
no other group of plants would possess (Kathiresan et
al., 2001).
Mangroves are distributed circumtropically. They are
confined in saline coastal sediment habitats in the
tropics and subtropics mainly between
latitudes 30° N and 30° S (Ramos, 2013). Within this
range, temperature, moisture and large currents
strongly affect their distribution (Kathiresan et al.,
2001). Rainfall also influences mangrove distribution,
largely by its effect on salinity (Ramos, 2013). Human
intervention, too, plays a role on mangrove
distribution.
Mangroves have massive ecological value (Kathiresan
et al., 2001). They unveil protection for coastal
erosion, securing coastal communities from storm
surges, waves, tides and currents. Above and beyond,
it exhibits facility of protected nursery area for marine
life and support for fisheries production and
aquaculture and functions as recreational grounds for
wildlife enthusiasts. Moreover, mangrove forests
provide important ecosystem services, and play
important roles in terrestrial and oceanic carbon
cycling (Liu et al., 2013).
Because climate change is progressively and globally
concerned, the potential of the mangrove forestry to
stock carbon is recently highlighted. This ecosystem is
made up of carbon-based life forms in plant biomass
and soil through litter fall. It significantly helps in
concentrating carbon dioxide in the atmosphere.
Although carbon sequestration has been assessed
frequently in terrestrial ecosystems, the carbon stocks
in mangrove forests have often been disregarded
especially here in the Philippines (Abino et al., 2014).
Philippines is bestowed with naturally rich mangrove
ecosystem with diverse floral and faunal species. The
Philippines alone hold 37 mangrove species out of
estimated 73 species recognized throughout the world
(Ramos, 2013). The province of Sarangani is one of
the places in the Philippines observed with coastal
resources including mangrove community. Using
combined data of municipal profiles and Provincial
Environment and Natural Resources Office (PENRO),
the mangrove forestlands were estimated at 267.6 ha
(De Jesus et al., 2001).
Despite this natural abundance, mangroves are
subjected to natural and human-induced
degradations specifically conversion to fish and
shrimp ponds that resulted to diminution (Abino et
al., 2014). Therefore, this study aims to assess species
diversity as well as to estimate above-ground
biomass, and C-stocks in one of the coastal zones in
Philippine archipelago.
Materials and methods
Study area
This study was carried out in Sarangani Province
located in southeastern Mindanao, geographically lies
between 05°56'24.255"- 05° 50’24.204"N and
125°16'51.154"-125°12’24.297"E (Fig. 1). The
researchers identified two areas as the study sites in
the municipalities of Malapatan and Glan. The precise
locations of each plot (Fig. 2) were determined
through the Global Positioning System (GPS).
Data collection
A total of 32 plots were established to determine the
species composition and the structure of the area.
Sixteen (16) plots were done in Glan Padidu, Glan
Sarangani Province and another 16 plots in
Malapatan, Sarangani Province. The plots were
J. Bio. Env. Sci. 2016
267 | Barcelete Jr et al.
randomly selected covering the different zones
including the landward, middle ward and seaward
mangroves. The plot dimension of 10 m × 10 m
constitutes the main plot, wherein mangroves within
the plot were measured and named. Purposive
sampling was implemented in establishing the plots
where mangroves are sufficient. Inside each plot,
girth size was measured from its breast height. In
terms of multiple branches aligning the breast height,
with the exception of family Rhizophoraceae, the
measure of the girth size of one branch will be added
to another branch to come up with a measurement.
Species located inside the sampling quadrates were
only considered for species inventory (Jumawan et
al., 2015).
Fig. 1. (A) Map of the Philippines, showing Malapatan and Glan, Sarangani Province in Mindanao area, (B and
C) Map showing the locations of the sampling sites in Malapatan and Glan, Sarangani Province respectively.
Species inventory
Mangrove species inside the plots were determined
and measured for further data analyses. Species and
some associated mangroves located outside the plot
but can be found in the area were also recorded.
Reliable identification guides were used to identify
mangrove species (Primavera et al., 2008;
Calumpong, 2007).
Identifying saplings and seedlings
Saplings are identified as young trees with girths of
less than 10 cm and a height of at least 1.3 cm.
Seedlings are young plants with a height of less than
1.3 m and are not branching. Saplings and seedlings
present inside the plot were counted, measured, and
identified.
Biodiversity measurements
Biodiversity index is the list of all the species found
within the area of interest and consists of Dominance,
Shannon, Evenness, Species Richness and Number of
individuals. Paleontological Statistics (PAST)
Software was used in measuring biodiversity indices.
Species diversity is described according to the
Shannon Index (H) as per the following equation:
In the formula given above, S is the total number of
species, N is the total number of individuals, and ni is
the number of individuals of the i-th species. ni/N is
equivalent to pi, the probability of finding the i-th
species (Magurran, 2004).
J. Bio. Env. Sci. 2016
268 | Barcelete Jr et al.
Data analysis
Mangrove forests are complex ecosystems that can be
found along intertidal zones and play a very
significant role in marine ecological balance.
Vegetation analysis provides a comprehensive species
list, definition of plant communities and the
identification of successional processes (Steinfield et
al., 2007).
Fig. 2. Sampling plots in Malapatan and Glan, Sarangani Province, Mindanao Island, Philippines.
These are the formulas used for the analysis:
Population Density = Number of Individuals/Total
area sampled.
Frequency = Number of plots in which a species
occurs/Total number of plots sampled.
Dominance = Total of basal area of each tree of a
species from all plots/Total area of all measured plots
Relative Density = (Number of individuals of a
species/Total number of individuals of all species) ×
100.
Relative Dominance = (Total basal area of a
species/Basal area of all species) × 100.
Relative Frequency = (Frequency of species/Total
frequency of all species in different plots) × 100.
Importance Value = Relative Density + Relative
Frequency + Relative Dominance solve.
The importance value index (IVI) which indicates the
structural importance of each species in the
community was obtained by adding the percentage
values of relative frequency (RF), relative dominance
(RDom) and relative density (Abino et al., 2014).
Carbon stored in mangroves ecosystem is measured
through the carbon present in the biomass.
Assessment of above ground biomass were calculated
using the allometric equation for mangroves, where
only parameters of diameter and wood density were
used. The maximum diameter of trees included in the
derivation of this equation was 49 cm with a total
number of 104 trees (Abino et al., 2014). Its
coefficient of determination (R2) is 0.98 which is,
comparably reliable with allometric equations derived
for natural stands (Chave et al., 2005; Hossain et al.,
2008; Kauffman and Cole, 2010). It was developed by
Komiyama et al. (2005) for Southeast Asian
mangroves. The following general equation was used:
were B stands for above-ground biomass (kg), ρ is
the wood density of the species (g/cm3), and D is the
diameter at breast height or dbh (cm) . The total
above-ground biomass of individual mangrove
J. Bio. Env. Sci. 2016
269 | Barcelete Jr et al.
species per plot in both sites was solved. The values
unraveled per plot were summed for all plots in each
site and averaged to get the mean biomass which was
then converted to tons per hectare (Abino et al.,
2014). Carbon pools of aboveground biomass were
then determined by multiplying the biomass carbon
concentration (percentage). Since the carbon
concentration of wood is usually a little less than 50%,
it is also common practice to convert biomass to
carbon by multiplying by 0.46–0.5 (Kauffman and
Donato, 2012). In this case, an average of 47% was
used to estimate carbon stock as based on published
carbon concentrations of dominant mangrove species
available on both sites.
Results and discussion
Species inventory
A total of ten (10) mangrove species belonging to five
(5) families were observed in both sites during the
sampling period. Eight (8) species were observed in
all plots established namely: Avicennia marina, A.
rumphiana, Bruguiera gymnorrhiza, B. sexangula,
Ceriops tagal, Rhizophora apiculata, R. mucronata
and Sonneratia alba (Table 1).
Table 1. List of mangrove species observed inside the plots of each sites.
Species Family Common name
Avicennia marina Avicenniaceae Bungalon, apiapi, miapi
Avicennina rumphiana Avicenniaceae Bungalon, apiapi, miapi
Bruguiera gymnorrhiza Rhizophoraceae Pototan, busain
Bruguiera sexangula Rhizophoraceae Pototan
Sonneratia alba Lythraceae Pagatpat
Ceriops tagal Rhizophoraceae Tungog, tangal
Rhizophora apiculata Rhizphoraceae Bakhaw lalaki
Rhizophora mucronata Rhizophoraceae Bakhaw babae
Nypa fruticans and Terminalia catappa were
associated mangrove species found outside the plots
(Tables 1 and 2). Family Rhizophoraceae got the
highest number of extant species with 5 mangrove
species. The recorded mangroves normally thrive
along the coastal municipalities of Sarangani Bay
based on the previous studies conducted by Mullet et
al, (2014) and Natividad et al, (2015) on vegetation
analyses, soil characteristics and community
structures in the area.
Table 2. List of associative mangrove species observed outside the plots of each sites.
Species Family Common name
Nypa fruticans Arecaceae Nipa, sasa
Terminalia Catappa Combretaceae Talisay
Only six (6) true mangrove species were found in
Malapatan together with the other two associated
mangroves. This number is quite lower compared to
the previous study conducted in 2015 by Mullet et al
where they listed 7 species. Xylocarpus granatum
and B. cylindrica were not found during the sampling
time however, three (3) new records were included
namely A. rumphiana, C. tagal and R. mucronata.
The establishment of plots could have affected the
number of recorded species which caused the
difference in the species.
Moreover, the mangroves found in Malapatan were
less copious having a total of 275 individuals
observed. S. alba dominated the mangrove forest in
the area with 122 individuals followed by R. apiculata
and R. mucronata with 122 and 28 individuals,
respectively (Table 3). It was also noted that the
J. Bio. Env. Sci. 2016
270 | Barcelete Jr et al.
vegetation in the area was not as dense compared to
the other site due to its close proximity to the
residential areas. The mangrove cover in the area is
only 53 hectares and is primarily composed of
secondary and primary growth trees (Mullet et al.,
2015). The mangrove forests in this municipality is
also frequently flooded and other man-made
disturbances are evident which conclude the limited
number of mangrove species observed.
Table 3. Species Composition and abundance of Mangrove species in Glan and Malapatan.
Species Glan Malapatan Total
Avicennia marina 22 21 43
Avicennia rumphiana 24 1 24
Bruguiera gymnorrhiza 1 0 1
Bruguiera sexangula 6 0 6
Sonneratia alba 45 122 164
Ceriops tagal 2 1 3
Rhizophora apiculata 299 102 401
Rhizophora mucronata 0 28 28
Total Number of Species found 399 275 674
On the other hand, seven (7) true mangrove species
were listed in Glan (Table 3). B. gymnorrhiza and B.
sexangula were present in the area and were not
found in the other site. The other species recorded in
Malapatan were also found in the site. R. mucronata
was also found in the area however, the number of
individuals were not counted because this species was
found outside the established plots.
Table 4. Mangrove seedlings and saplings observed in Glan, Sarangani Province.
Mangrove Species Seedlings Saplings Total
A. marina 7 2 9
A. rumphiana 16 0 16
B. sexangula 0 1 1
R. apiculata 18 112 130
S. alba 23 6 24
There were a total of 399 individuals observed in the
area dominated by R. apiculata with a count of 299
individuals (Table 3). Mangroves found in Glan were
of high abundance due to the absence of man-made
activities thus having vast number of mangroves
observed in each plot. Some plots however contained
fewer individuals but it can be explained by the huge
diameter at breast height of some of the species. The
mangrove forest in the site is primarily composed of
primary, secondary and tertiary growth trees from
seaward to landward due to its undisturbed nature
that means it is not influenced by man-made
activities as compared to the other site. Also,
rehabilitation is done in the area and the locals are
well-informed of the importance of the mangal
community within the vicinity.
Regeneration of saplings and seedlings
A total of 6 species regenerated on both sites
including A. marina, A. rumphiana, B. sexangula, R.
apiculata, R. mucronata and S. alba (Tables 4 and 5).
Regeneration in Glan was relatively higher with a
total of 185 individuals of which 64 are seedlings and
121 are saplings. This was dominated by R. apiculata
which had the highest regeneration count of 130
individuals. Meanwhile, Malapatan seedlings and
J. Bio. Env. Sci. 2016
271 | Barcelete Jr et al.
saplings were lower in number with only 85
individuals from three species namely R. apiculata,
R. mucronata and S. alba. Of the total count, 49 were
seedlings while 36 were saplings the seedlings mainly
from R. apiculata and S. alba. The presence of
regeneration indicates that the both mangrove forests
are thriving despite the relatively low counts.
Table 5. Mangrove Seedlings and saplings observed in Malapatan, Sarangani Province.
Mangrove Species Seedlings Saplings Total
R. apiculata 42 12 54
R. murcronata 5 3 8
S.alba 2 21 23
49 36 85
Biodiversity measurements
Table 6 shows the results on the biodiversity indices
in both of the mangrove forests. The mangroves in
Glan were found to be higher in terms of species
richness (2.4375), no. of individuals (23.5625) and
dominance (0.678113) which concludes that the
mangroves found in the said area is undisturbed and
is growing naturally. On the other hand, the
mangroves found in Malapatan were found to be
higher in terms of Shannon (0.780331) and evenness
(0.925631) which concludes that the mangroves
found in the said area has been influenced by man-
made activities that also resulted in the distribution of
mangroves were uniform throughout the area. Data
findings showed that the results in Malapatan were
quite different with the former study by Mullet et al
(2015). However, the difference must be verified
further to have definite assumptions regarding
biodiversity measurements on the area.
Table 6. Biodiversity Indices of Mangrove Species found in Glan and Malapatan.
Biodiversity Indices Glan Malapatan
Species Richness 2.25 2.4375
No. of individuals 23.5625 16.4375
Evenness 0.0810881 0.925631
Shannon 0.522669 0.780331
Dominance 0.678113 0.492769
Table 7. Vegetation Analysis of Mangroves on Glan Padidu, Glan, Sarangani Province
Species RPD(%) RF(%) RDOM(%) SIV Ranking
R.apiculata 74.27 41.67 4.38 1
S.alba 11.14 36.11 4.30 2
A.marina 5.84 11.11 0.64 3
A.rumphiana 6.37 2.78 0.35 4
B.sexangula 1.59 2.78 0.03 5
C.tagal 0.53 2.78 0.08 6
B.gymnorrhiza 0.27 2.78 0.23 7
Vegetation analysis
The vegetation analysis of mangroves in Glan as
shown in Table 7 revealed that the species R.
apiculata ranked highest in terms of Relative
Population Density (RPD), Relative Frequency (RF)
and Relative Dominance (RDOM) with values of
74.27%, 41.67% and 4.38%, respectively. This is then
followed by S. alba with RPD, RF and RDOM values
of 11.14%, 36.11% and 4.30%, respectively. R.
apiculata was present in high abundance in the site
and dominated the entire mangrove forest.
J. Bio. Env. Sci. 2016
272 | Barcelete Jr et al.
Table 8. Vegetation Analysis of Mangroves on Malapatan, Sarangani Province.
Species RPD(%) RF(%) RDOM(%) SIV Ranking
S.alba 46.39 40 81.24 1
R.apiculata 35.36 40 13 2
R.mucronata 9.89 10 0.78 3
A.marina 7.89 7.59 4.87 4
C.tagal 0.38 2.50 0.11 5
Consequently, results on the vegetation analysis of
mangroves in Malapatan coincides with the former
study especially on the species with high values. S.
alba had an RPD value of 46.39%, RF value of 40%
and RDOM value of 81% (Table 8). This species were
found in high numbers with sizes (based on the dbh
measurements) relatively bigger than the other
species. On the other hand, C. tagal obtained the
lowest values having RPD, RF and RDOM values of
0.38%, 2.50% and 0.11%, respectively as marked by
its less abundance in the area (Table 8).
Above-ground biomass and carbon stock analysis
The above-ground biomass of the mangrove trees was
determined through establishing relationship
between biomass of the trees and the readily
measured main stem diameter. Main stem diameter
was expressed as the diameter at 1.37 m above the
ground (dbh), or in the case of Rhizophora, the
diameter above the highest stilt root (Kauffman and
Donato, 2012).
Fig 4. Bar chart showing the results of Carbon Stocks in (A) Glan Padidu, (B) Malapatan, Sarangani Province.
On the stand level, the mangrove forest of Glan has an
average above-ground biomass of 901.17 t ha- ranging
from 194.07 t ha- to 4567.93 t ha- while Malapatan
mangal has a total biomass of 366.70 t ha- covering
from 4.08 t ha- to 1306.02 t ha-. The total carbon pool
on the first site varied from 91.21 t C ha- to as high as
2146.93 t C ha- with a mean value of 423.55 t C ha-.
The second site on the other hand has an average
carbon stock of 172.35 t C ha- extending from 1.92 t C
ha- to 613.83 t C ha- based on the carbon
concentration used. These carbon density values have
carbon dioxide equivalents that were sequestered and
stored in the above-ground biomass. In detail, the
above-ground biomass in Glan with its total carbon
pool is equivalent to 1554.43 t CO2 ha- reaching from
334.75 t.
J. Bio. Env. Sci. 2016
273 | Barcelete Jr et al.
CO2 ha- to as much as 7879.22 t CO2 ha- . On the other
hand, Malapatan with its carbon stock component
sequestered an equivalent of 632.51 t CO2 ha- ranging
from 7.03 t CO2 ha- to 2252.75 t CO2 ha-.
The two sites were comparably significant for their
high carbon stock potential and the ability of the
mangroves flourishing in these mangals show
promising results in sequestering carbon. These
mangrove forests contribute extensively in mitigating
climate change due to the continuous increase of
carbon levels in the atmosphere which is a global
concern.
Conclusion
Figure 4 shows that a higher diversity index was
perceived in the natural mangrove stand in Glan
Padidu, Glan compared to Lun Padidu, Malapatan
due to natural and human made disturbance.
Attributed to the dominance of some species located
on the two sites were R. apiculata and S. alba,
respectively. Moreover, Glan Padidu mangrove forest
also has a greater carbon pool value. The large tree
girths and high density of species observed in these
forests show a great potential to sequester and store
large amount of atmospheric carbon. It is also note
worthy that this study quantifies mangrove tree
biomass in view of carbon trading as significant in
mitigating the effects of global warming.
Acknowledgement
The researchers would like to thank the people of
Brgy. Glan Padidu, Glan Sarangani, especially to the
barangay officials for lending us their assistance in
guiding us through the mangrove fields and giving us
basic information regarding the mangroves. The
researchers would also like to give thanks to Rabor
Family for lending us their aid in terms of sheltering
our needs in Brgy. Lun Padidu, Malapatan Glan
Sarangani. Lastly, the researchers would like to
extend our gratitude to Prof. Ron Bigsang for giving
us help on analyzing carbon pool present in the
mangrove stand.
References
Abino C, Castillo Jose Alan A, Lee, Young Jin.
2014. Species Diversity, Biomass, and Carbon Stock
Assessments of a Natural Mangrove Forest in
Palawan, Philippines. Pakistan Journal of Botany,
46(6), 1955-1962.
Calumpong, Hilconida P. 2007. Field Guide to the
Common Mangroves, Seagrasses and Algae of the
Philippines
Chave J, Andalo C, Brown C, Cairns MA,
Chambers JQ, Eamus D, Folster D, Fromard
F, Higuchi N, Kira T, Lescure JP, Nelson BW,
Ogawa H, Puig H, Riera B, Yamakura T. 2005.
Tree allometry and improved estimation of carbon
stocks and balance in tropical forests. Oecologia 145,
87-99.
De Jesus Edgar A, Diamante-Fabunan,
Dolores Ariadne D, Nañola Cleto L, White,
Alan T, Cabangon Hermenegildo J. 2001.
Mangrove Community. Coastal Environmental Profile
of the Sarangani Bay Area Mindanao, Philippines.
Coastal Resource Management Project of the
Department of Environment and Natural Resources
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Hossain M, Othman S, Bujang JS, Kusnan JS.
2008. Net primary productivity of Bruguiera
parviflora (Wight & Arn.) dominated mangrove forest
at Kuala Selangor, Malaysia. For. Ecol. Manage 255,
179-182.
Liu, Hongxiao, Hai Ren, Dafeng Hui, Wenqing
Wang, Baowen Liao, Qingxian Cao. 2014.
Carbon stocks and potential carbon storage in the
mangrove forests of China. Journal of Environmental
Management 133, 86–93.
Kathiresan K, Bingham BL. 2001. Biology of
Mangroves and Mangrove Ecosystems. Advances in
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Kauffman JB, Cole TG. 2010. Micronesian
mangrove forest structure and tree response to a
severe typhoon. Wetlands 30, 1077-1084.
Kauffman JB, Donato DC. 2012. Protocols for the
measurement, monitoring and reporting of structure,
biomass and carbon stocks in mangrove forests.
Working Paper 86, 1-33.
Mullet Earl Kevin C, Haydn Lacorte Giuseppe,
Hamiladan Rea Mae A. 2014 Assessment of
Mangrove Species and its relation to soil substrates in
Malapatan, Sarangani Province, Philippines. Journal
of Biodiversity and Environmental Sciences 5(4),
100-107.
Nipithwittaya, Sureeporn and Bualert, Surat.
2012. Above Ground Carbon Sequestration in
Mangrove Forest Filtration System. Journal of
Applied Sciences 12, 1537-1546.
Natividad. 2015. Vegetation Analysis and
Community Structure of Mangrove in Alabel and
Maasim Sarangani. Journal Agricultural and
Biological science 10(3), 97-102
Primavera JH. Ph. D. 2009. Field Guide to
Philippine Mangroves.
Ramos Ma, Junemie Hazel L. 2013. Field Guide
to Mangrove Identification and Community Structure
Analysis.
Rath Anthony B. 2015. Mangrove Importance.
World Wild Fund for Nature.

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Species Diversity and Above-ground Carbon Stock Assessments in Selected Mangrove Forests of Malapatan and Glan, Sarangani Province, Philippines - JBES

  • 1. J. Bio. Env. Sci. 2016 265 | Barcelete Jr et al. RESEARCH PAPER OPEN ACCESS Species diversity and above-ground carbon stock assessments in selected mangrove forests of Malapatan and Glan, Sarangani Province, Philippines Ricky C. Barcelete Jr* , Eva Mae F. Palmero1 , Bhegie May G. Buay1 , Cyril B. Apares1 , Lanny R. Dominoto1 , Harold Lipae1 , Ma. Luisa N. Cabrera1 , Mark Anthony J. Torres2 , Elani A. Requieron1 1 Science Department, Mindanao State University, General Santos, Philippines 2 Department of Biological Sciences, Mindanao State University, Iligan, Philippines Article published on February 28, 2016 Key words: Sonneratia alba, Rhizophora apiculata, C-stocks. Abstract Mangrove ecosystems are known for being the rainforest of the sea. Philippines is bestowed with this naturally rich mangrove ecosystem with diverse floral and faunal species. Despite this natural abundance, mangrove ecosystems are subjected to natural and human induced degradations specifically conversion to fish shrimp ponds that resulted in diminution aside from its effect on terrestrial and oceanic carbon cycling and could also affect its important role in terms of terrestrial and oceanic carbon cycling. This study is conducted to determine the mangrove diversity, distribution and the above-ground biomass and C-stocks in Glan and Malapatan, Sarangani Province. Purposive sampling is implemented in establishing the plots on both sites. Results show eight (8) mangrove species belonging to four (4) families are observed in both areas. Data also reveal that the mangrove ecosystem in Glan Padidu, Glan is undisturbed. Rhizophora apiculata and Sonneratia alba are found to be dominant on the two sites. Because of the large tree girths and high density of species observed on the studied areas, both forests have the potential to sequester and store large amount of atmospheric carbon. Thus, this study quantifies mangrove tree biomass in view of carbon trading as significant in lessening the effects of global warming. *Corresponding Author: Ricky C. Barcelete Jr.  ricky_barcelete@yahoo.com Journal of Biodiversity and Environmental Sciences (JBES) ISSN: 2220-6663 (Print) 2222-3045 (Online) Vol. 8, No. 2, p. 265-274, 2016 http://www.innspub.net
  • 2. J. Bio. Env. Sci. 2016 266 | Barcelete Jr et al. Introduction Mangrove forest is also known as the “rainforest of the sea”. It grows well on mudflats and banks of tropical and subtropical rivers and coastlines, existing at the boundary of land and water and receiving nutrients from both environments (Ramos, 2013). Mangroves are salt tolerant trees (halophytes) because they contain a complex salt filtration system and complex root system to cope with salt water immersion and wave action. They are also anoxic, adapted to the low oxygen conditions of waterlogged mud. They have these highly developed morphological, biological, ecological and physiological adaptations to extreme conditions that no other group of plants would possess (Kathiresan et al., 2001). Mangroves are distributed circumtropically. They are confined in saline coastal sediment habitats in the tropics and subtropics mainly between latitudes 30° N and 30° S (Ramos, 2013). Within this range, temperature, moisture and large currents strongly affect their distribution (Kathiresan et al., 2001). Rainfall also influences mangrove distribution, largely by its effect on salinity (Ramos, 2013). Human intervention, too, plays a role on mangrove distribution. Mangroves have massive ecological value (Kathiresan et al., 2001). They unveil protection for coastal erosion, securing coastal communities from storm surges, waves, tides and currents. Above and beyond, it exhibits facility of protected nursery area for marine life and support for fisheries production and aquaculture and functions as recreational grounds for wildlife enthusiasts. Moreover, mangrove forests provide important ecosystem services, and play important roles in terrestrial and oceanic carbon cycling (Liu et al., 2013). Because climate change is progressively and globally concerned, the potential of the mangrove forestry to stock carbon is recently highlighted. This ecosystem is made up of carbon-based life forms in plant biomass and soil through litter fall. It significantly helps in concentrating carbon dioxide in the atmosphere. Although carbon sequestration has been assessed frequently in terrestrial ecosystems, the carbon stocks in mangrove forests have often been disregarded especially here in the Philippines (Abino et al., 2014). Philippines is bestowed with naturally rich mangrove ecosystem with diverse floral and faunal species. The Philippines alone hold 37 mangrove species out of estimated 73 species recognized throughout the world (Ramos, 2013). The province of Sarangani is one of the places in the Philippines observed with coastal resources including mangrove community. Using combined data of municipal profiles and Provincial Environment and Natural Resources Office (PENRO), the mangrove forestlands were estimated at 267.6 ha (De Jesus et al., 2001). Despite this natural abundance, mangroves are subjected to natural and human-induced degradations specifically conversion to fish and shrimp ponds that resulted to diminution (Abino et al., 2014). Therefore, this study aims to assess species diversity as well as to estimate above-ground biomass, and C-stocks in one of the coastal zones in Philippine archipelago. Materials and methods Study area This study was carried out in Sarangani Province located in southeastern Mindanao, geographically lies between 05°56'24.255"- 05° 50’24.204"N and 125°16'51.154"-125°12’24.297"E (Fig. 1). The researchers identified two areas as the study sites in the municipalities of Malapatan and Glan. The precise locations of each plot (Fig. 2) were determined through the Global Positioning System (GPS). Data collection A total of 32 plots were established to determine the species composition and the structure of the area. Sixteen (16) plots were done in Glan Padidu, Glan Sarangani Province and another 16 plots in Malapatan, Sarangani Province. The plots were
  • 3. J. Bio. Env. Sci. 2016 267 | Barcelete Jr et al. randomly selected covering the different zones including the landward, middle ward and seaward mangroves. The plot dimension of 10 m × 10 m constitutes the main plot, wherein mangroves within the plot were measured and named. Purposive sampling was implemented in establishing the plots where mangroves are sufficient. Inside each plot, girth size was measured from its breast height. In terms of multiple branches aligning the breast height, with the exception of family Rhizophoraceae, the measure of the girth size of one branch will be added to another branch to come up with a measurement. Species located inside the sampling quadrates were only considered for species inventory (Jumawan et al., 2015). Fig. 1. (A) Map of the Philippines, showing Malapatan and Glan, Sarangani Province in Mindanao area, (B and C) Map showing the locations of the sampling sites in Malapatan and Glan, Sarangani Province respectively. Species inventory Mangrove species inside the plots were determined and measured for further data analyses. Species and some associated mangroves located outside the plot but can be found in the area were also recorded. Reliable identification guides were used to identify mangrove species (Primavera et al., 2008; Calumpong, 2007). Identifying saplings and seedlings Saplings are identified as young trees with girths of less than 10 cm and a height of at least 1.3 cm. Seedlings are young plants with a height of less than 1.3 m and are not branching. Saplings and seedlings present inside the plot were counted, measured, and identified. Biodiversity measurements Biodiversity index is the list of all the species found within the area of interest and consists of Dominance, Shannon, Evenness, Species Richness and Number of individuals. Paleontological Statistics (PAST) Software was used in measuring biodiversity indices. Species diversity is described according to the Shannon Index (H) as per the following equation: In the formula given above, S is the total number of species, N is the total number of individuals, and ni is the number of individuals of the i-th species. ni/N is equivalent to pi, the probability of finding the i-th species (Magurran, 2004).
  • 4. J. Bio. Env. Sci. 2016 268 | Barcelete Jr et al. Data analysis Mangrove forests are complex ecosystems that can be found along intertidal zones and play a very significant role in marine ecological balance. Vegetation analysis provides a comprehensive species list, definition of plant communities and the identification of successional processes (Steinfield et al., 2007). Fig. 2. Sampling plots in Malapatan and Glan, Sarangani Province, Mindanao Island, Philippines. These are the formulas used for the analysis: Population Density = Number of Individuals/Total area sampled. Frequency = Number of plots in which a species occurs/Total number of plots sampled. Dominance = Total of basal area of each tree of a species from all plots/Total area of all measured plots Relative Density = (Number of individuals of a species/Total number of individuals of all species) × 100. Relative Dominance = (Total basal area of a species/Basal area of all species) × 100. Relative Frequency = (Frequency of species/Total frequency of all species in different plots) × 100. Importance Value = Relative Density + Relative Frequency + Relative Dominance solve. The importance value index (IVI) which indicates the structural importance of each species in the community was obtained by adding the percentage values of relative frequency (RF), relative dominance (RDom) and relative density (Abino et al., 2014). Carbon stored in mangroves ecosystem is measured through the carbon present in the biomass. Assessment of above ground biomass were calculated using the allometric equation for mangroves, where only parameters of diameter and wood density were used. The maximum diameter of trees included in the derivation of this equation was 49 cm with a total number of 104 trees (Abino et al., 2014). Its coefficient of determination (R2) is 0.98 which is, comparably reliable with allometric equations derived for natural stands (Chave et al., 2005; Hossain et al., 2008; Kauffman and Cole, 2010). It was developed by Komiyama et al. (2005) for Southeast Asian mangroves. The following general equation was used: were B stands for above-ground biomass (kg), ρ is the wood density of the species (g/cm3), and D is the diameter at breast height or dbh (cm) . The total above-ground biomass of individual mangrove
  • 5. J. Bio. Env. Sci. 2016 269 | Barcelete Jr et al. species per plot in both sites was solved. The values unraveled per plot were summed for all plots in each site and averaged to get the mean biomass which was then converted to tons per hectare (Abino et al., 2014). Carbon pools of aboveground biomass were then determined by multiplying the biomass carbon concentration (percentage). Since the carbon concentration of wood is usually a little less than 50%, it is also common practice to convert biomass to carbon by multiplying by 0.46–0.5 (Kauffman and Donato, 2012). In this case, an average of 47% was used to estimate carbon stock as based on published carbon concentrations of dominant mangrove species available on both sites. Results and discussion Species inventory A total of ten (10) mangrove species belonging to five (5) families were observed in both sites during the sampling period. Eight (8) species were observed in all plots established namely: Avicennia marina, A. rumphiana, Bruguiera gymnorrhiza, B. sexangula, Ceriops tagal, Rhizophora apiculata, R. mucronata and Sonneratia alba (Table 1). Table 1. List of mangrove species observed inside the plots of each sites. Species Family Common name Avicennia marina Avicenniaceae Bungalon, apiapi, miapi Avicennina rumphiana Avicenniaceae Bungalon, apiapi, miapi Bruguiera gymnorrhiza Rhizophoraceae Pototan, busain Bruguiera sexangula Rhizophoraceae Pototan Sonneratia alba Lythraceae Pagatpat Ceriops tagal Rhizophoraceae Tungog, tangal Rhizophora apiculata Rhizphoraceae Bakhaw lalaki Rhizophora mucronata Rhizophoraceae Bakhaw babae Nypa fruticans and Terminalia catappa were associated mangrove species found outside the plots (Tables 1 and 2). Family Rhizophoraceae got the highest number of extant species with 5 mangrove species. The recorded mangroves normally thrive along the coastal municipalities of Sarangani Bay based on the previous studies conducted by Mullet et al, (2014) and Natividad et al, (2015) on vegetation analyses, soil characteristics and community structures in the area. Table 2. List of associative mangrove species observed outside the plots of each sites. Species Family Common name Nypa fruticans Arecaceae Nipa, sasa Terminalia Catappa Combretaceae Talisay Only six (6) true mangrove species were found in Malapatan together with the other two associated mangroves. This number is quite lower compared to the previous study conducted in 2015 by Mullet et al where they listed 7 species. Xylocarpus granatum and B. cylindrica were not found during the sampling time however, three (3) new records were included namely A. rumphiana, C. tagal and R. mucronata. The establishment of plots could have affected the number of recorded species which caused the difference in the species. Moreover, the mangroves found in Malapatan were less copious having a total of 275 individuals observed. S. alba dominated the mangrove forest in the area with 122 individuals followed by R. apiculata and R. mucronata with 122 and 28 individuals, respectively (Table 3). It was also noted that the
  • 6. J. Bio. Env. Sci. 2016 270 | Barcelete Jr et al. vegetation in the area was not as dense compared to the other site due to its close proximity to the residential areas. The mangrove cover in the area is only 53 hectares and is primarily composed of secondary and primary growth trees (Mullet et al., 2015). The mangrove forests in this municipality is also frequently flooded and other man-made disturbances are evident which conclude the limited number of mangrove species observed. Table 3. Species Composition and abundance of Mangrove species in Glan and Malapatan. Species Glan Malapatan Total Avicennia marina 22 21 43 Avicennia rumphiana 24 1 24 Bruguiera gymnorrhiza 1 0 1 Bruguiera sexangula 6 0 6 Sonneratia alba 45 122 164 Ceriops tagal 2 1 3 Rhizophora apiculata 299 102 401 Rhizophora mucronata 0 28 28 Total Number of Species found 399 275 674 On the other hand, seven (7) true mangrove species were listed in Glan (Table 3). B. gymnorrhiza and B. sexangula were present in the area and were not found in the other site. The other species recorded in Malapatan were also found in the site. R. mucronata was also found in the area however, the number of individuals were not counted because this species was found outside the established plots. Table 4. Mangrove seedlings and saplings observed in Glan, Sarangani Province. Mangrove Species Seedlings Saplings Total A. marina 7 2 9 A. rumphiana 16 0 16 B. sexangula 0 1 1 R. apiculata 18 112 130 S. alba 23 6 24 There were a total of 399 individuals observed in the area dominated by R. apiculata with a count of 299 individuals (Table 3). Mangroves found in Glan were of high abundance due to the absence of man-made activities thus having vast number of mangroves observed in each plot. Some plots however contained fewer individuals but it can be explained by the huge diameter at breast height of some of the species. The mangrove forest in the site is primarily composed of primary, secondary and tertiary growth trees from seaward to landward due to its undisturbed nature that means it is not influenced by man-made activities as compared to the other site. Also, rehabilitation is done in the area and the locals are well-informed of the importance of the mangal community within the vicinity. Regeneration of saplings and seedlings A total of 6 species regenerated on both sites including A. marina, A. rumphiana, B. sexangula, R. apiculata, R. mucronata and S. alba (Tables 4 and 5). Regeneration in Glan was relatively higher with a total of 185 individuals of which 64 are seedlings and 121 are saplings. This was dominated by R. apiculata which had the highest regeneration count of 130 individuals. Meanwhile, Malapatan seedlings and
  • 7. J. Bio. Env. Sci. 2016 271 | Barcelete Jr et al. saplings were lower in number with only 85 individuals from three species namely R. apiculata, R. mucronata and S. alba. Of the total count, 49 were seedlings while 36 were saplings the seedlings mainly from R. apiculata and S. alba. The presence of regeneration indicates that the both mangrove forests are thriving despite the relatively low counts. Table 5. Mangrove Seedlings and saplings observed in Malapatan, Sarangani Province. Mangrove Species Seedlings Saplings Total R. apiculata 42 12 54 R. murcronata 5 3 8 S.alba 2 21 23 49 36 85 Biodiversity measurements Table 6 shows the results on the biodiversity indices in both of the mangrove forests. The mangroves in Glan were found to be higher in terms of species richness (2.4375), no. of individuals (23.5625) and dominance (0.678113) which concludes that the mangroves found in the said area is undisturbed and is growing naturally. On the other hand, the mangroves found in Malapatan were found to be higher in terms of Shannon (0.780331) and evenness (0.925631) which concludes that the mangroves found in the said area has been influenced by man- made activities that also resulted in the distribution of mangroves were uniform throughout the area. Data findings showed that the results in Malapatan were quite different with the former study by Mullet et al (2015). However, the difference must be verified further to have definite assumptions regarding biodiversity measurements on the area. Table 6. Biodiversity Indices of Mangrove Species found in Glan and Malapatan. Biodiversity Indices Glan Malapatan Species Richness 2.25 2.4375 No. of individuals 23.5625 16.4375 Evenness 0.0810881 0.925631 Shannon 0.522669 0.780331 Dominance 0.678113 0.492769 Table 7. Vegetation Analysis of Mangroves on Glan Padidu, Glan, Sarangani Province Species RPD(%) RF(%) RDOM(%) SIV Ranking R.apiculata 74.27 41.67 4.38 1 S.alba 11.14 36.11 4.30 2 A.marina 5.84 11.11 0.64 3 A.rumphiana 6.37 2.78 0.35 4 B.sexangula 1.59 2.78 0.03 5 C.tagal 0.53 2.78 0.08 6 B.gymnorrhiza 0.27 2.78 0.23 7 Vegetation analysis The vegetation analysis of mangroves in Glan as shown in Table 7 revealed that the species R. apiculata ranked highest in terms of Relative Population Density (RPD), Relative Frequency (RF) and Relative Dominance (RDOM) with values of 74.27%, 41.67% and 4.38%, respectively. This is then followed by S. alba with RPD, RF and RDOM values of 11.14%, 36.11% and 4.30%, respectively. R. apiculata was present in high abundance in the site and dominated the entire mangrove forest.
  • 8. J. Bio. Env. Sci. 2016 272 | Barcelete Jr et al. Table 8. Vegetation Analysis of Mangroves on Malapatan, Sarangani Province. Species RPD(%) RF(%) RDOM(%) SIV Ranking S.alba 46.39 40 81.24 1 R.apiculata 35.36 40 13 2 R.mucronata 9.89 10 0.78 3 A.marina 7.89 7.59 4.87 4 C.tagal 0.38 2.50 0.11 5 Consequently, results on the vegetation analysis of mangroves in Malapatan coincides with the former study especially on the species with high values. S. alba had an RPD value of 46.39%, RF value of 40% and RDOM value of 81% (Table 8). This species were found in high numbers with sizes (based on the dbh measurements) relatively bigger than the other species. On the other hand, C. tagal obtained the lowest values having RPD, RF and RDOM values of 0.38%, 2.50% and 0.11%, respectively as marked by its less abundance in the area (Table 8). Above-ground biomass and carbon stock analysis The above-ground biomass of the mangrove trees was determined through establishing relationship between biomass of the trees and the readily measured main stem diameter. Main stem diameter was expressed as the diameter at 1.37 m above the ground (dbh), or in the case of Rhizophora, the diameter above the highest stilt root (Kauffman and Donato, 2012). Fig 4. Bar chart showing the results of Carbon Stocks in (A) Glan Padidu, (B) Malapatan, Sarangani Province. On the stand level, the mangrove forest of Glan has an average above-ground biomass of 901.17 t ha- ranging from 194.07 t ha- to 4567.93 t ha- while Malapatan mangal has a total biomass of 366.70 t ha- covering from 4.08 t ha- to 1306.02 t ha-. The total carbon pool on the first site varied from 91.21 t C ha- to as high as 2146.93 t C ha- with a mean value of 423.55 t C ha-. The second site on the other hand has an average carbon stock of 172.35 t C ha- extending from 1.92 t C ha- to 613.83 t C ha- based on the carbon concentration used. These carbon density values have carbon dioxide equivalents that were sequestered and stored in the above-ground biomass. In detail, the above-ground biomass in Glan with its total carbon pool is equivalent to 1554.43 t CO2 ha- reaching from 334.75 t.
  • 9. J. Bio. Env. Sci. 2016 273 | Barcelete Jr et al. CO2 ha- to as much as 7879.22 t CO2 ha- . On the other hand, Malapatan with its carbon stock component sequestered an equivalent of 632.51 t CO2 ha- ranging from 7.03 t CO2 ha- to 2252.75 t CO2 ha-. The two sites were comparably significant for their high carbon stock potential and the ability of the mangroves flourishing in these mangals show promising results in sequestering carbon. These mangrove forests contribute extensively in mitigating climate change due to the continuous increase of carbon levels in the atmosphere which is a global concern. Conclusion Figure 4 shows that a higher diversity index was perceived in the natural mangrove stand in Glan Padidu, Glan compared to Lun Padidu, Malapatan due to natural and human made disturbance. Attributed to the dominance of some species located on the two sites were R. apiculata and S. alba, respectively. Moreover, Glan Padidu mangrove forest also has a greater carbon pool value. The large tree girths and high density of species observed in these forests show a great potential to sequester and store large amount of atmospheric carbon. It is also note worthy that this study quantifies mangrove tree biomass in view of carbon trading as significant in mitigating the effects of global warming. Acknowledgement The researchers would like to thank the people of Brgy. Glan Padidu, Glan Sarangani, especially to the barangay officials for lending us their assistance in guiding us through the mangrove fields and giving us basic information regarding the mangroves. The researchers would also like to give thanks to Rabor Family for lending us their aid in terms of sheltering our needs in Brgy. Lun Padidu, Malapatan Glan Sarangani. Lastly, the researchers would like to extend our gratitude to Prof. Ron Bigsang for giving us help on analyzing carbon pool present in the mangrove stand. References Abino C, Castillo Jose Alan A, Lee, Young Jin. 2014. Species Diversity, Biomass, and Carbon Stock Assessments of a Natural Mangrove Forest in Palawan, Philippines. Pakistan Journal of Botany, 46(6), 1955-1962. Calumpong, Hilconida P. 2007. Field Guide to the Common Mangroves, Seagrasses and Algae of the Philippines Chave J, Andalo C, Brown C, Cairns MA, Chambers JQ, Eamus D, Folster D, Fromard F, Higuchi N, Kira T, Lescure JP, Nelson BW, Ogawa H, Puig H, Riera B, Yamakura T. 2005. Tree allometry and improved estimation of carbon stocks and balance in tropical forests. Oecologia 145, 87-99. De Jesus Edgar A, Diamante-Fabunan, Dolores Ariadne D, Nañola Cleto L, White, Alan T, Cabangon Hermenegildo J. 2001. Mangrove Community. Coastal Environmental Profile of the Sarangani Bay Area Mindanao, Philippines. Coastal Resource Management Project of the Department of Environment and Natural Resources supported by the United States Agency for International Development, 22-37. Hossain M, Othman S, Bujang JS, Kusnan JS. 2008. Net primary productivity of Bruguiera parviflora (Wight & Arn.) dominated mangrove forest at Kuala Selangor, Malaysia. For. Ecol. Manage 255, 179-182. Liu, Hongxiao, Hai Ren, Dafeng Hui, Wenqing Wang, Baowen Liao, Qingxian Cao. 2014. Carbon stocks and potential carbon storage in the mangrove forests of China. Journal of Environmental Management 133, 86–93. Kathiresan K, Bingham BL. 2001. Biology of Mangroves and Mangrove Ecosystems. Advances in Marine Biology 40, 81-251.
  • 10. J. Bio. Env. Sci. 2016 274 | Barcelete Jr et al. Kauffman JB, Cole TG. 2010. Micronesian mangrove forest structure and tree response to a severe typhoon. Wetlands 30, 1077-1084. Kauffman JB, Donato DC. 2012. Protocols for the measurement, monitoring and reporting of structure, biomass and carbon stocks in mangrove forests. Working Paper 86, 1-33. Mullet Earl Kevin C, Haydn Lacorte Giuseppe, Hamiladan Rea Mae A. 2014 Assessment of Mangrove Species and its relation to soil substrates in Malapatan, Sarangani Province, Philippines. Journal of Biodiversity and Environmental Sciences 5(4), 100-107. Nipithwittaya, Sureeporn and Bualert, Surat. 2012. Above Ground Carbon Sequestration in Mangrove Forest Filtration System. Journal of Applied Sciences 12, 1537-1546. Natividad. 2015. Vegetation Analysis and Community Structure of Mangrove in Alabel and Maasim Sarangani. Journal Agricultural and Biological science 10(3), 97-102 Primavera JH. Ph. D. 2009. Field Guide to Philippine Mangroves. Ramos Ma, Junemie Hazel L. 2013. Field Guide to Mangrove Identification and Community Structure Analysis. Rath Anthony B. 2015. Mangrove Importance. World Wild Fund for Nature.