J. Bio. & Env. Sci. 2023
76 | Dapar et al.
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Diversity, distribution and conservation status of mangrove
species in the Municipality of Biliran, Biliran Island, Philippines
Litlen P. Dapar*1
, Romel Quinte2
, Ma Opelia M. Moreno3
, Melanie P. Moncada4
,
Florante P. Sabejon5
1
Department of Forest Science, School of Agribusiness and Forest Resource Management,
Biliran Province State University, Biliran Campus, Biliran, Philippines
2
Department of Agriculture, School of Agri-Fisheries, Biliran Province State University,
Biliran Campus, Biliran, Philippines
3
Department of Forest Science, School of Agribusiness and Forest Resource Management,
Biliran Province State University, Biliran Campus, Biliran, Philippines
4
Department of Forest Science, School of Agribusiness and Forest Resource Management,
Biliran Province State University, Biliran Campus, Biliran, Philippines
5
Department of Forest Science, School of Agribusiness and Forest Resource Management,
Biliran Province State University, Biliran Campus, Biliran, Philippines
Article published on May 16, 2023
Key words: Biodiversity, Mangroves, IUCN, Biliran Island
Abstract
We determined the diversity of mangrove species and their conservation status in the municipality of Biliran to serve as
baseline for conservation and protection of mangal ecosystems in the island. Thirty-two quadrats with a size of 10×10 m
were established and each mangrove tree inside the plots was identified. The numbers of individuals per species were
counted and diversity indices were computed. Results revealed 13 mangrove species belonging to 7 families including
Avicennia rumphiana, A. marina, A. alba, Rhizophora apiculata, R. stylosa, R. mucronata, Ceriops tagal, Bruguiera
sp., Sonneratia alba, Exoecaria agallocha, Scyphiphora hydrophyllacea, Xylocarpus granatum, and Brownlowia tersa.
Majority of the mangrove species belonged to Rhizophoraceae family. R. apiculata was the most abundant while B. tersa
was the least abundant species. Mangroves like C. tagal, R. apiculata, and A. marina were generalist species because they
were found in all of the study sites, whereas A. rumphiana, A. alba, S. hydrophyllacea, B. tersa, R. mucronata, and
Bruguiera sp. were specialist because they were only found in 1 study site. A. rumphiana was the only mangrove listed as
Vulnerable (VU) based on IUCN Red List of Threatened Species. The mean values of the following indices were obtained:
H’= 1.1984, DMn= 0.7124, J= 0.6877 and D= 0.3877. Mangrove diversity in Biliran municipality was very low with a highly
even distribution of species and uniform distribution of individuals. Since mangal ecosystems in the municipality of
Biliran are facing natural and anthropogenic disturbances, the local government unit should prioritize mangrove forest
conservation and rehabilitation.
*Corresponding Author: Litlen P. Dapar  litlenphils_84@yahoo.com
Journal of Biodiversity and Environmental Sciences (JBES)
ISSN: 2220-6663 (Print) 2222-3045 (Online)
Vol. 22, No. 5, p. 76-86, 2023
http://www.innspub.net
J. Bio. & Env. Sci. 2023
77 | Dapar et al.
Introduction
Mangroves ecosystems are mostly composed of
halophytic tree and shrub species that are regularly
expose to fluctuations in water level, hydrodynamic
energy, salinity, nutrient availability, and anoxia
(Friess, 2016). Despite thriving in a dynamic and
physiologically stressful location, a plethora of coastal
and terrestrial fauna are associated with this
vegetation including fish, crustaceans, snakes and
mammals. In addition to their unique biodiversity
value, mangroves are largely important habitats due
to some tangible provisioning ecosystem services they
provide to the local coastal populations such as
timber, charcoal, non-timber forest products and
fish/shellfish. The United Nations Environment
Programme (2014) further cited that mangrove
ecosystem provides millions of people with food,
clean water, raw materials and resilience against
future climate change impacts including increasing
storm intensity and sea level rise. For instance, when
super typhoon Haiyan struck the central Philippines,
areas with mangrove forests suffered significantly less
damage as the trees acted as shield from the strong
winds and waves (Ranada, 2014).
Faustino et al. (2020) noted that mangrove forests in
the Philippines have been continuously dwindling in
terms of forest cover and diversity due to
anthropogenic activities which include cutting of trees
for the production of firewood, charcoal, and building
materials, and residential, urban and industrial
development, and conversion to agriculture (Maneja,
2006; Bitantos et al., 2017) as well as natural
disturbances. In view of these challenges, it is
important to conduct baseline studies to give not only
a benchmark of an area’s biodiversity but a picture of
its overall importance in the landscape (Flora and
Fauna International, 2014). A baseline study can
highlight areas of importance for biodiversity
conservation, identify threats to species and habitats,
and help understand how local communities use and
value resources.
Fortes and Salmo (2017) cited that mangrove studies
in the Philippines are initially categorized under
seven topics including taxonomy, physiology,
economic uses, biogeography, ecology, biodiversity,
and conservation and management. However,
information on species composition and diversity
studies of mangroves from the different parts of the
country remains limited and scarce (Baleta and
Casalamitao, 2016). Recent local biodiversity studies
and vegetational analysis on mangroves have been
carried out in Surigao del Norte (Goloran et al.,
2020), Camarines Sur (Faustino et al., 2020),
Oriental Mindoro (Raganas et al., 2020), Palawan
(Dangan-Galon et al., 2016), Camotes island (Lillo et
al., 2022), Timaco Mangrove Swamp in Cotabato City
(Cano-Mangaoang et al., 2022), Samar island
(Mendoza and Alura, 2001), Zamboanga Sibugay
(Bitantos et al., 2017), Pangasinan (Rosario et al.,
2021), Aurora (Rotaquio et al., 2017), Cagayan Valley
(Calicdan et al., 2017), Isabela (Baleta and
Casalamitao, 2016), Aklan (Barrientos and Apolonio,
2017), Quezon province (Abantao et al., 2015), and
Leyte island (Bobon-Carnice et al., 2021). To date,
mangrove studies on the island of Biliran is not
documented, particularly in the municipality of
Biliran where a large portion of mangrove forest in
the village of Sangalang became a wasteland when
many mangrove trees and associated species died
during the onslaught of tropical depression (TD)
Urduja in 2017. Thus, this study was conducted to
gather scientific-based data that can serve as a
baseline in determining the diversity and
conservation status of mangrove species based on the
International Union for the Conservation of Nature
(IUCN) Red List of Threatened Species. Such baseline
can be used in prioritizing areas for conservation and
protection of mangal ecosystems in the island,
especially with the ongoing threats of both
anthropogenic and natural disturbances.
Material and methods
Establishment of Sampling Plots and Identification
of Mangrove Species
Five coastal villages with mangrove areas in the
municipality of Biliran, namely: Burabod, Busali,
Sangalang, Julita, and Villa Enage were selected as
study sites based on the preliminary survey (Fig. 1).
J. Bio. & Env. Sci. 2023
78 | Dapar et al.
The village of Bato was excluded due to the
dominance of Nypa fruticans Wurmb. in its
mangrove area. The methodology followed by
Faustino et al. (2020) was modified based on the field
conditions. Thus, only a total of 32 quadrats or plots
with a size of 10×10 m were established.
Inside the plots, each mangrove tree was identified
down to the species level using a field guide
(Primavera, 2009). The number of individuals per
species were counted and recorded on a field
notebook. Presence of anthropogenic disturbances
whether inside or outside the plots were also noted.
Fig. 1. Map of the location of study sites in the municipality of Biliran showing: A) Busali and Burabod; and B)
Villa Enage, Sangalang, and Julita.
Sources: DENR 8-FLUP Team and Biliran LGU MTWG; Google Maps.
Analysis of Data
Using the data on the number of individuals for each
species, the following indices were computed:
1. Species Richness (Menhinick Index)
(DMn) 

√
where:
S = total no. of species observed
N = total number of individuals in the sample
DMn = Menhinick Index
2. Species Diversity (Shannon-Wiener Index)
H’ = ∑ Pi

ln Pi
where:
H’ = Shannon-Wiener Index
S = no. of species
pi = proportion of individuals of the abundance of the
ith species expressed as proportion of total abundance
(ni/N)
ln= natural logarithm
3. Equitability (Pielou’s Evenness Index)
J = H’/ln(S)
where:
H’ = Shannon-Wiener Index of Diversity
S = total number of species
ln = natural logarithm
J = Pielou’s Evenness Index
4. Species Dominance (Simpson Index)
D =
∑ 
 
where:
n= number of individuals of the ith species
N = total number of individuals
∑ = the sum of the calculations
D = Simpson Index
J. Bio.  Env. Sci. 2023
79 | Dapar et al.
Result and discussion
Species Composition of Mangroves
A total of 13 mangrove species belonging to 7 families
could be found thriving in the coastal villages of
Biliran municipality (Table 1). The identified species
were Avicennia rumphiana Hallier f., Avicennia
marina (Forssk.) Vierh., and Avicennia alba Blume
from Avicenniaceae family; Rhizophora apiculata
Blume, Rhizophora stylosa Griff., Rhizophora
mucronata Lam., Ceriops tagal (Perr.) C. B. Rob.,
and Bruguiera sp. from Rhizophoraceae family;
Sonneratia alba Sm. from Sonneratiaceae family;
Exoecaria agallocha L. from Euphorbiaceae family;
Scyphiphora hydrophyllacea C. F. Gaertn. from
Rubiaceae; Xylocarpus granatum J. Koenig from
Meliaceae family; and Brownlowia tersa (L.)
Kosterm. from Tiliaceae family. Majority of the
mangrove species found in the study sites belonged to
Rhizophoraceae family (57.31%), followed by
Avicenniaceae family (29.68%) (Fig. 2). Only 0.23%
of the mangroves belonged to Meliaceae family.
Table 1. Mangrove species that can be found in the
municipality of Biliran.
Family Name Species Name Local Name
Avicenniaceae Avicennia rumphiana Miapi
Avicenniaceae Avicennia marina Miapi
Avicenniaceae Avicennia alba Miapi
Rhizophoraceae Rhizophora apiculata
Bakhaw
lalaki
Rhizophoraceae Rhizophora stylosa Bakhaw bato
Rhizophoraceae
Rhizophora
mucronata
Bakhaw
babae
Rhizophoraceae Ceriops tagal Tangal
Rhizophoraceae Bruguiera sp. Pototan
Sonneratiaceae Sonneratia alba Pagatpat
Euphorbiaceae Exoecaria agallocha Lipata
Rubiaceae
Scyphiphora
hydrophyllacea
Nilad
Meliaceae Xylocarpus granatum Tabigi
Tiliaceae Brownlowia tersa Magaromon
Fig. 2. Composition of mangroves based on families.
Abundance, Occurrence, and Distribution of
Mangrove Species
The abundance, occurrence, and distribution of
mangrove species in the municipality of Biliran
differed based on the study sites (Table 2).
A total of 438 individuals of mangrove species were
counted in the study sites, in which, R. apiculata
Blume was the most abundant (165 individuals) while
B. tersa (L.) Kosterm. was the least abundant species
(1 individual).
The 3 mangrove species, C. tagal (Perr.) C.B. Rob.,
R. apiculata Blume, and A. marina (Forssk.) Vierh.
were found in all of the study sites whereas S. alba
Sm. Were also found in 4 study sites, except in
Busali. R. stylosa Griff. and X. granatum J. Koenig
were seen thriving in Sangalang and Villa Enage
while E. agallocha L. were found in both Sangalang
and Busali.
On the other hand, 4 species including A. rumphiana
Hallier f., A. alba Blume, S. hydrophyllacea C. F.
Gaertn., and B. tersa (L.) Kosterm. seemed to be
limited to Sangalang while R. mucronata Lam. and
Bruguiera sp. were seemingly restricted to Julita and
Villa Enage, respectively.
Table 2. Abundance, occurrence, and distribution of
mangroves per study site in the municipality of Biliran.
Species
Study Site Total
Number of
Individuals
Burabod Busali SangalangJulita
Villa
Enage
A. alba X X 71 X X 73
A. rumphiana X X 10 X X 10
A. marina 20 9 1 6 11 47
R. stylosa X X 1 X 8 9
R. mucronata X X X 2 X 2
R. apiculata 16 6 21 61 61 165
C. tagal 1 9 58 2 2 72
Bruguiera sp. X X X X 3 3
S. alba 3 X 8 13 23 47
E. agallocha X 1 3 X X 4
S. hydrophyllacea X X 3 X X 3
X. granatum X X 1 X 1 2
B. tersa X X 1 X X 1
Total 40 25 178 84 111 438
Note: X= Not present
J. Bio.  Env. Sci. 2023
80 | Dapar et al.
Fig. 3. Both natural and anthropogenic disturbances are threatening the existence of A. rumphiana in Sangalang.
Diversity of Mangrove Species
The species richness (DMn), dominance (D), evenness
(J) and diversity (H’) of mangrove species per study
site in the municipality of Biliran is shown in Fig. 4.
The mean species richness obtained was DMn= 0.7124
and mean species diversity was H’= 1.1984, in which
Sangalang recorded both the highest species richness
value of DMn = 0.8245 and species diversity value of
H’= 1.5390. However, this mean H’ index value could
be considered as very low in terms of diversity. On the
other hand, the mean equitability index obtained was
J’= 0.6877, in which Busali had the highest
equitability value of J= 0.8706. This J value indicated
a highly even distribution of the mangrove species in
the study sites. In terms of dominance, the mean
species dominance value obtained was D=0.3877, in
which Julita had the highest dominance value of
D=0.5575. This D value suggested a uniform
distribution of individuals among the mangrove
species in the study area.
Table 3. Species richness (DMn), dominance (D), equitability (J) and diversity (H’) index of mangrove species per
study site in the municipality of Biliran.
Index
Study Site
Total Mean
Burabod Busali Sangalang Julita Villa Enage
Species Richness 0.6325 0.8000 0.8245 0.5455 0.7593 3.5618 0.7124
Species Diversity 0.9996 1.2070 1.5390 0.8876 1.3590 5.9922 1.1984
Equitability 0.7210 0.8706 0.6420 0.5515 0.6533 3.4384 0.6877
Dominance 0.4163 0.3184 0.2851 0.5575 0.3614 1.9387 0.3877
Conservation Status of Mangrove Species
Among the 13 identified mangrove species, A.
rumphiana Hallier f. is the only mangrove species
listed as Vulnerable (VU) based on IUCN Red List of
Threatened Species of 2022 while the rest of the
species were either listed as Least Concern (LC) or
Not Evaluated (NE) (Table 4). This mangrove species
could only be found in Sangalang where both natural
and anthropogenic disturbances are threatening the
existence of this species (Fig. 4). Large tracts of
mangrove areas in this village were decimated due to
mudslide and flooding events caused by tropical
depression Urduja in 2017. Insect infestation of the
mangroves is highly likely because of the presence of
many caterpillars. Indications of anthropogenic
disturbances were also evident in the site including
J. Bio.  Env. Sci. 2023
81 | Dapar et al.
presence of cutting marks in 2 mangrove trees and
degrading pieces of metallic fishing net.
Table 4. Mangrove species and their ecological
status based on IUCN Red List of Threatened Species
in the municipality of Biliran.
Family Name Species Name Ecological Status
Avicenniaceae Avicennia rumphiana Vulnerable (VU)
Avicenniaceae Avicennia marina Least concern (LC)
Avicenniaceae Avicennia alba Least concern (LC)
RhizophoraceaeRhizophora apiculata Least concern (LC)
RhizophoraceaeCeriops tagal Least concern (LC)
RhizophoraceaeRhizophora stylosa Least concern (LC)
RhizophoraceaeRhizophora mucronata Least concern (LC)
RhizophoraceaeBruguiera sp. -
Sonneratiaceae Sonneratia alba Least concern (LC)
Euphorbiaceae Exoecaria agallocha Not evaluated ()
Rubiaceae
Scyphiphora
hydrophyllacea
Least concern (LC)
Meliaceae Xylocarpus granatum Least concern (LC)
Tiliaceae Brownlowia tersa Not evaluated (NE)
Note: The symbol - means that ecological status could
not be determined since it was not identified down to
the species level.
Discussion
Species Composition of Mangroves
Noor et al. (2012) cited that species within
Rhizophoraceae family are among the most
significant and most widely distributed mangal
species. Species dominance of Rhizophoraceae family
could even reach 90% of the total vegetation, in which
optimal growth usually occurs in deeply inundated
land and humus-rich soil. Families of Avicenniaceae
and Rhizophoraceae often dominate the mangal
population in terms of number of species and
abundance (Hogarth, 2013). In Indonesia, the
Rhizophoraceae family primarily consisting of
Bruguiera gymnorrhiza (L.) Lam., R. mucronata
Lam., R. apiculata Blume, R. stylosa Griff., and C.
tagal (Perr.) C.B. Rob. was found more often than the
other families of mangroves (Utina et al., 2019). They
have highly developed morphological and
physiological adaptations to extreme intertidal
environments, and are predisposed with genes which
are crucial for increased capability of stress tolerance
including defense against salt and oxidative stress,
and development of adaptive traits like vivipary (Guo
et al., 2017). All Rhizophora taxa are also
characterized by large water-buoyant propagules with
a remarkable ability for long-distance
dispersal (Rabinowitz, 1978). The strong enclosure of
its young shoots by conspicuous rounded or flattened
stipules and colleter exudates offer structural and
mechanical protection, shielding the young shoots of
these mangrove plants from their harsh environments
(Sheue et al., 2012).
Along with Rhizophoraceae family, species from
Avicenniaceae family also form the dominant plant
communities of mangrove forests (Duke, 1991). As an
important member of the mangal formation, all
species of this family exhibit adaptations convergent
with those of other mangroves such as tolerance of
high salt concentrations, excretion of hypersaline
solutions on both leaf surfaces via subsessile
glandular hairs, xerophytic specializations of leaves,
sea-water dispersed viviparous fruits, and soft mud
catching hypocotyl of the embryo that allows
immediate growth of the seedling (Sanders, 1997).
Abundance, Occurrence, and Distribution of
Mangrove Species
Mangrove species including C. tagal (Perr.) C. B.
Rob., R. apiculata Blume, and A. marina (Forssk.)
Vierh. were generalist species because they were
found in all of the study sites, whereas A. rumphiana
Hallier f., A. alba Blume, S. hydrophyllacea C. F.
Gaertn., B. tersa (L.) Kosterm., R. mucronata Lam.,
and Bruguiera sp. were specialist species because
they were only found in one study site. Kirsch (2021)
cited that generalist species have a wider range of
environmental tolerance and utilize a variety of
resources by possessing widely applicable features
that are not constricted to a narrow function. On the
contrary, ecological specialist species have narrowly
evolved characteristics that optimize their fitness in
their local environment at the cost of vulnerability to
disturbance and a high level of dependence on their
available niche. It has been shown that habitat
heterogeneity tends to favor generalist species
temporally and spatially, while specialists benefit
from homogeneous habitat conditions (Büchi and
Vuilleumier, 2014; Marvier et al., 2004; Devictor et
al., 2008; Verberk et al., 2010). Büchi and
Vuilleumier (2014) further explained that life-history
J. Bio.  Env. Sci. 2023
82 | Dapar et al.
traits such as niche breadth and dispersal ability, and
environmental factors like disturbance, spatial
heterogeneity, and autocorrelation could influence
the coexistence of specialist and generalist species.
Diversity of Mangrove Species
Rosario et al. (2021) interpreted H’ index of diversity
as very low (1.999), low (2.000-2.499), moderate
(2.500-2.999), high (3.000-3.499), or very high
(3.500). The very low diversity of mangroves in the
municipality of Biliran was comparable to the
mangrove forests in Tacloban City, Leyte (Patindol
and Casas, 2019), Binmaley, Pangasinan (Rosario et
al., 2021), Dumanquillas Bay, Zamboanga Sibugay
((Bitantos et al., 2017), Cancabato Bay, Leyte (Bobon-
Carnice et al., 2021), and Mabini, Davao de Oro
(Manual et al., 2022). Morris et al. (2014) after
Shannon (1948) explained that in a highly diverse
system, an unknown individual could belong to any
species which often leads to a high uncertainty in
predicting its identity. In a less diverse system
dominated by one or a few species, it is easier to
predict the identity of unknown individuals and there
is less uncertainty in the system.
Fatonah et al. (2021) emphasized that species
evenness values equal to or close to 1 means the
species are evenly distributed. It is also categorized as
uneven (0.00-0.40), moderately even (0.41-0.60),
and highly even (0.61-1.00). Equitability represents
the degree to which individuals are split among
species with low values indicating that one or a few
species dominate, and high values indicating that
relatively equal numbers of individuals belong to each
species (Morris et al., 2014). Meanwhile, dominance
values close to one (1) imply a clumping of individuals
in a few species whereas values close to zero (0) mean
a more uniform distribution of individuals among the
species (Doherty et al., 2011). The dominance has a
range value of 0 where all taxa are equally distributed
to 1 where one taxon dominates the community
completely (Manual et al., 2002).
A variety of both biotic and abiotic factors play a role
in influencing the diversity of mangrove species and
their distributional patterns. Mangroves are forest
types consisting of all plants along the coast or river
estuary which are affected by tides and interacting
with their environment (Irsadi et al., 2019). Duke et
al. (1998) stated that numerous factors affect the
distribution of mangrove plants including direction of
sea currents, presence of land barriers, and species-
specific characteristics such as their water-buoyant
propagules, establishment success and growth
development rate, and tolerance limits and growth
responses. Ellison (2021) further explained that
mangrove ecosystem diversity and dynamics are
influenced by physical factors of temperature, coastal
typology, ocean currents and land barriers, wave
action and sediment supply, river catchment
discharge and sediment yield, and tidal range and
inundation frequencies. Factors of gradients and tidal
ranges control the lateral extent of mangroves
through inundation frequency, and factors
influencing accretion rates in the context of relative
sea level change can shift or eliminate mangrove
extents over time.
Conservation Status of Mangrove Species
Triest et al. (2021) reported that the IUCN Red List of
Threatened Species considered A. rumphiana Hallier
f. is a species with vulnerable status because of its
patchy distribution, being uncommon in some areas,
and declining population. It also thrives in the upper
part of the intertidal zone where it is most vulnerable
to human activities and habitat destruction. Chan et
al. (2022) explained that population trend of this
species is decreasing and the mangrove habitat within
this species range has declined at least 30% from
1980 to 2005. However, there are no available data to
estimate the decline of population as well as no
measures have been in placed for the conservation
and protection of this species.
Conclusion
Results revealed 13 mangroves belonging to 7 families
including A. rumphiana, A. marina, A. alba, R.
apiculata, R. stylosa, R. mucronata, C. tagal,
Bruguiera sp., S. alba, E. agallocha, S.
hydrophyllacea, X. granatum, and B. tersa. Majority
of the mangroves belonged to Rhizophoraceae family.
J. Bio.  Env. Sci. 2023
83 | Dapar et al.
R. apiculata was the most abundant while B. tersa
was the least abundant species. C. tagal, R. apiculata,
and A. marina were found in all of the study sites
whereas S. alba. was found in 4 study sites. R. stylosa
and X. granatum thrived in Sangalang and Villa
Enage while E. agallocha inhabited Sangalang and
Busali. A. rumphiana, A. alba, S. hydrophyllacea,
and B. tersa were limited to Sangalang while R.
mucronata and Bruguiera sp. were restricted to
Julita and Villa Enage, respectively.
The mean values of the following indices were
obtained: H’= 1.1984, DMn= 0.7124, J= 0.6877 and D=
0.3877. Mangrove diversity in Biliran municipality
was very low with a highly even distribution of species
and uniform distribution of individuals. A.
rumphiana was the only mangrove species listed as
Vulnerable (VU) based on IUCN Red List of
Threatened Species while rests of the species were
either listed as Least Concern (LC) or Not Evaluated
(NE).
Recommendation(S)
The mangal forests of Biliran municipality are facing
both natural and anthropogenic disturbances. To
protect these fragile ecosystems, a multi-sectoral and
science-based conservation and rehabilitation
programs must be formulated and undertaken. The
local government unit of Biliran, Biliran Province
State University-Biliran Campus, and People’s
Organizations in the municipality of Biliran must
work hand-in hand to ensure the sustainability of the
programs. Since the diversity of mangrove species in
the municipality of Biliran was very low, tree planting
activities that take into account zonation patterns of
mangrove species and site-species matching
principles are also recommended.
To capture on-ground status and conditions of
mangroves in the entire Biliran island, similar
baseline studies must be conducted in the other
municipalities, particularly in the island
municipality of Maripipi due to the known effects of
island biogeography on distributional patterns and
diversity of species.
Acknowledgements
Our heartfelt thanks to Dr. Randy A. Villarin, Dean of
the School of Agribusiness and Forest Resource
Management, faculty and students of the Department
of Forest Science, and the Farmers and Fisherfolks
Association (FFA) of Sangalang for their support and
assistance in the conduct of this study.
References
Abantao SC, Apacible TC, Cortez SP, Pereda
LT, Yllano OB. 2015. Mangrove species diversity
and on-site impact assessment of mangal coastal
areas. Expert Opinion on Environmental Biology
4(3), 100-105. DOI:10.4172/2325-9655.1000122.
Baleta FN, Casalamitao RSJ. 2016. Species
composition, diversity and abundance of mangroves
along the estuarine Area of Maligaya, Palanan,
Isabela, Philippines. International Journal of
Fisheries and Aquatic Studies 4(2), 303-307.
Barrientos K, Apolonio JW. 2017. Species
diversity and soil carbon sequestration potential of
mangrove species at Katunggan It Ibajay (KII) Eco-
Park in Aklan, Philippines. PRISM: The Official
Research Publication of Negros Oriental State
University, Negros Oriental. ISSN: 0119-4607/EISSN:
2546-0390. Available at: https://ssrn.com /abstract=
Biliran Provincial MDG Team. 2010. Status
Report on the Millennium Development Goals Using
CBMS Data. Province of Biliran - National Economic
and Development Authority. Available at: http://
www. neda.gov.ph /econreports... /MDGs /... /PR.
Bitantos BL, Abucay MD, Dacula JA, Recafort
RD. 2017. Mangrove in the grove: diversity, species
composition, and habitat in Pamintayan,
Dumanquillas Bay, Philippines. Advances in
Environmental Science Bioflux 9(3), 183-192.
Bobon-Carnice PA, Magayes MR, Gacus EE,
Operario EC, Martija MAA. 2021. Aboveground
carbon storage and species diversity of mangrove
stand in Leyte Island, Philippines. ARADMAN: A
Multidisciplinary Research Journal 1(1), 50-69.
J. Bio.  Env. Sci. 2023
84 | Dapar et al.
Büchi L, Vuilleumier S. 2014. Coexistence of
specialist and generalist species is shaped by dispersal
and environmental factors. The American Naturalist
183(5), 612-624.
Calicdan MA, Rebancos C, Ancog R, Baguinon
N. 2015. Assessment of mangrove flora of Palaui
Island Protected Landscape and Seascape (PIPLS)
San Vicente, Sta. Ana Cagayan Valley, Philippines.
Asian Journal of Conservation Biology 4(1), 15-19.
ISSN 2278-7666.
Cano-Mangaoang C, Amino ZC, Mastur BB.
2022. Status of mangrove forest in Timaco Mangrove
Swamp, Cotabato City, Philippines. Journal of
Threatened Taxa 14(11), 22080-22085.
DOI: 10.11609 /jott.7826.14.11.22080-22085.
Chan EWC, Tangah J, Kezuka M, Chan HT.
2022. Botany, distribution, phytochemistry and
bioactivities of mangrove plants VI: Avicennia
rumphiana. ISME/GLOMIS Electronic Journal
20(2), 13-16.
Dangan-Galon F, Dolorosa RG, Sespeñe JS,
Mendoza NI. 2016. Diversity and structural
complexity of mangrove forest along Puerto Princesa
Bay, Palawan Island, Philippines. Journal of Marine
and Island Cultures 5(2), 118-125.
Devictor V, Julliard R, Jiguet F. 2008.
Distribution of specialist and generalist species along
spatial gradients of habitat disturbance and
fragmentation. Oikos 117, 507-514.
Doherty JH, Harris C, Hartley L. 2011.
Calculating Biological Diversity: Teaching Issues and
Experiments in Ecology. Ecological Society of
America. Available at: https://tiee.esa.org/vol/v7/
experiments /doherty/resources/diversity.doc.
Duke N, Duke C, Ball MC, Ellison JC. 1998.
Factors Influencing Biodiversity and Distributional
Gradients in Mangroves. Global Ecology and
Biogeography Letters 7(1), 27-47.
Duke NC. 1991. A systematic revision of the
mangrove genus Avicennia (Avicenniaceae)
Australasia. Australian Systematic Botany 4, 299-
324. DOI: 10.1071/SB9910299.
Ellison JC. 2021. Factors Influencing Mangrove
Ecosystems. In: Rastogi RP, Phulwaria M, Gupta
DK, Ed. Mangroves: Ecology, Biodiversity and
Management. New Delhi, India: Springer p. 97-115.
Fatona S, Hamidy R, Mulyadi A, Friyeldi E.
2021. Floristic composition and stand structure of
mangrove forests with varying vegetation conditions
in Sungai Apit, Siak, Riau, Indonesia. Biodiversitas
22, 3972-3983. DOI: 10.13057/biodiv /d220945.
Faustino AZ, Madela HL, Castor RG, Muroda
AP, Chavez MNP. 2020. Community mapping and
vegetational analysis of the mangrove forest in
Calabanga, San Miguel Bay, Philippines. E3S Web of
Conferences 147(2), 02017.
Flora and Fauna International. 2017.
Biodiversity Baselines for Development and
Conservation. Available at: https://www.faunaflora.
org/app/uploads/2017/12/FFI2014_Biodiversity-
baselines -for-development-and-conservation.pdf.
Fortes MD, Salmo S III. 2017. Technical
presentations. Status of mangrove research and
management in the Philippines: Challenges and
opportunities. Ateneo Journals Online 2(2), 50-60.
Friess DA. 2016. Quick guide to mangrove forests.
Current Biology 26, R739-R755.
Goloran AB, Demetillo MT, Betco GL. 2020.
Mangrove assessment and diversity in coastal area of
Barangay Cagdianao, Claver, Surigao del Norte,
Philippines. International Journal of Environmental
Sciences and Natural Resources 26(3), 556-188.
Gregorio N, Herbohn J, Tripoli R, Pasa A.
2020. A Local Initiative to Achieve Global Forest and
Landscape Restoration Challenge—Lessons Learned
from a Community-Based Forest Restoration Project
in Biliran Province, Philippines. Forests 11(4), 475.
J. Bio.  Env. Sci. 2023
85 | Dapar et al.
Guo W, Wu H, Zhang Z, Yang C, Hu L, Shi X,
Jian S, Shi S, Huang Y. 2017. Comparative
analysis of transcriptomes in Rhizophoraceae
provides insights into the origin and adaptive
evolution of mangrove plants in intertidal
environments. Frontiers in Plant Science Section
Evolutionary and Population Genetics 8, 00795.
Hogarth PJ. 2013. Mangrove Ecosystems:
Rhizophoraceae. In: Levin Sa, 2nd Ed. Encyclopedia of
Biodiversity: Academic Press, p: 10-22.
Irsadi A, Anggoro S, Soeprobowati TR. 2019.
Environmental Factors Supporting Mangrove
Ecosystem in Semarang-Demak Coastal Area. E3S
Web of Conferences 125, 01021.
IUCN. 2022. IUCN Red List of Threatened Species.
Available at https://www.iucnredlist.org.
Kirsch AN. 2021. Defining plant ecological
specialists and generalists: Building a framework for
identification and classification [Master’s thesis,
Minnesota State University, Mankato]. Cornerstone:
A Collection of Scholarly and Creative Works for
Minnesota State University, Mankato. Available at:
https://cornerstone.lib. mnsu.edu/etds/1175.
Lillo EP, Malaki AB, Alcazar SMT, Rosales R,
Redoblado BR, Diaz JLB, Pantinople EM,
Nuevo RU. 2022. Composition and diversity of
Mangrove species in Camotes Island, Cebu,
Philippines. Journal of Marine and Island Cultures
11(1), 2212-6821. DOI: 10.21463/jmic. 2022.11.1.11.
Maneja RH. 2006. Analysis of the responses of
mangrove ecosystems in the Philippines to climate
change. Agusan River Basin Mangrove Wildlife
Conservation Network Website. Available at:
http://www.freewebs.com/arbm wcnetwork/.
Manual AMB, Gabato NAS, Jetuya QB,
Alimbon JA. 2022. Floristic composition, structure,
and diversity of mangroves in the coastal areas of
Mabini, Davao de Oro, Philippines. Biodiversitas
23(9), 4887-4893. DOI: 10.13057/biodiv/d230958.
Marvier M, Kareiva P, Neubert MG. 2004. Habitat
destruction, fragmentation, and disturbance promote
invasion by habitat generalists in a multispecies
metapopulation. Risk Analysis 24, 869- 878.
Mendoza AB, Alura DP. 2001. Mangrove
Structure on the Eastern Coast of Samar Island,
Philippines. In: Stott DE, Mohtar RH, Steinhardt GC,
Ed. Sustaining the Global Farm. Indiana USA: Purdue
University p. 423-425.
Morris EK, Caruso T, Buscot F, Fischer M,
Hancock C, Maier TS, Meiners T, Muller C,
Obermaier E, Prati D, Socher SA, Sonnemann
I, Waschke N, Wubet T, Wurst S, Rillig MC.
2014. Choosing and using diversity indices: insights
for ecological applications from the German
Biodiversity Exploratories. Ecology and Evolution
4(18), 3514- 3524. DOI: 10.1002/ece3.1155.
Noor YR, Khazali M, Suryadiputra INN. 2012.
The Third Printing Guide for Mangrove Indonesia in
2012. Wetlands International Indonesia Programme.
Bogor, Indonesia.
Patindol T, Casas JE. 2019. Species diversity and
composition of mangroves in Tacloban City
Philippines. Annals of Tropical Research 41, 67-75.
DOI:10.32945/atr4126.2019.
PhilAtlas. 2023. Biliran, Biliran Profile - PhilAtlas.
Available at: https://www.philatlas.com/visayas/
r08/biliran/biliran.html
Primavera JH. 2009. Field Guide to Philippine
Mangroves. Philippine Tropical Forest Conservation
Foundation, Inc. and Zoological Society of London.
Rabinowitz D. 1978. Dispersal properties of
mangrove propagules. Biotropica 10, 47-57.
Raganas AFM, Magcale-Macandog DB. 2020.
Physicochemical factors influencing zonation
patterns, niche width and tolerances of dominant
mangroves in southern Oriental Mindoro,
Philippines. Ocean Life 4(2), 51-62.
J. Bio.  Env. Sci. 2023
86 | Dapar et al.
Ranada P. 2014. The importance of mangrove
forests. The Manila Times. Available at:
https://www./manilatimes.net/importance-
mangrove-forests/14404 5/.
Rosario GR, dela Peña RV, de Guzman R,
Abalos RS, Tamayo E. 2021. Species composition
and diversity of mangroves in the riverbanks of
Barangay Basing, Binmaley, Pangasinan. Journal of
Natural and Allied Sciences 5(1), 51-59.
Rotaquio EL, Nakagoshi N, Rotaquio RL. 2007.
Species composition of mangrove forests in Aurora,
Philippines: A special reference to Kandelia candel
(L.) Druce. Journal of International Development and
Cooperation 13(1), 61-78.
Sanders RW. 1997. The Avicenniaceae in the
Southeastern United States. Harvard Papers in
Botany 1(10), 81-92.
Sheue CR, Chen Y, Yang Y. 2012. Stipules and
colleters of the mangrove Rhizophoraceae:
morphology, structure and comparative significance.
Botanical Studies 53, 243-254.
Triest L, Del Socorro A, Gado VJ, Mazo AM,
Sierens T. 2021. Avicennia genetic diversity
andfine-scaled structure influenced by coastal
proximity of mangrove fragments. Frontiers in
Marine Science Section Global Change and the Future
Ocean 8, 643982. DOI: 10.3389/fmars.2021.643982.
United Nations Environment Programme.
2014. The Importance of Mangroves to People: A Call
to Action. In: van Bochove J, Sullivan E, Nakamura T,
Ed. United Nations Environment Programme World
Conservation Monitoring Centre, Cambridge.
Utina R, Katili AS, Lapolo N, Dangkua T. 2019.
Short Communication: The composition of mangrove
species in coastal area of Banggai District, Central
Sulawesi, Indonesia. Biodiversitas 20(3), 840-846.
DOI: 10.13057/biodiv/d200 330.
Verberk W, van der Velde G, Esselin H. 2010.
Explaining abundance-occupancy relationships in
specialists and generalists: a case study on aquatic
macroinvertebrates in standing waters. Journal of
Animal Ecology 79, 589-601.

Diversity, distribution and conservation status of mangrove species in the Municipality of Biliran, Biliran Island, Philippines

  • 1.
    J. Bio. &Env. Sci. 2023 76 | Dapar et al. RE RE RE RESEARCH SEARCH SEARCH SEARCH PAPER PAPER PAPER PAPER OPEN ACCESS OPEN ACCESS OPEN ACCESS OPEN ACCESS Diversity, distribution and conservation status of mangrove species in the Municipality of Biliran, Biliran Island, Philippines Litlen P. Dapar*1 , Romel Quinte2 , Ma Opelia M. Moreno3 , Melanie P. Moncada4 , Florante P. Sabejon5 1 Department of Forest Science, School of Agribusiness and Forest Resource Management, Biliran Province State University, Biliran Campus, Biliran, Philippines 2 Department of Agriculture, School of Agri-Fisheries, Biliran Province State University, Biliran Campus, Biliran, Philippines 3 Department of Forest Science, School of Agribusiness and Forest Resource Management, Biliran Province State University, Biliran Campus, Biliran, Philippines 4 Department of Forest Science, School of Agribusiness and Forest Resource Management, Biliran Province State University, Biliran Campus, Biliran, Philippines 5 Department of Forest Science, School of Agribusiness and Forest Resource Management, Biliran Province State University, Biliran Campus, Biliran, Philippines Article published on May 16, 2023 Key words: Biodiversity, Mangroves, IUCN, Biliran Island Abstract We determined the diversity of mangrove species and their conservation status in the municipality of Biliran to serve as baseline for conservation and protection of mangal ecosystems in the island. Thirty-two quadrats with a size of 10×10 m were established and each mangrove tree inside the plots was identified. The numbers of individuals per species were counted and diversity indices were computed. Results revealed 13 mangrove species belonging to 7 families including Avicennia rumphiana, A. marina, A. alba, Rhizophora apiculata, R. stylosa, R. mucronata, Ceriops tagal, Bruguiera sp., Sonneratia alba, Exoecaria agallocha, Scyphiphora hydrophyllacea, Xylocarpus granatum, and Brownlowia tersa. Majority of the mangrove species belonged to Rhizophoraceae family. R. apiculata was the most abundant while B. tersa was the least abundant species. Mangroves like C. tagal, R. apiculata, and A. marina were generalist species because they were found in all of the study sites, whereas A. rumphiana, A. alba, S. hydrophyllacea, B. tersa, R. mucronata, and Bruguiera sp. were specialist because they were only found in 1 study site. A. rumphiana was the only mangrove listed as Vulnerable (VU) based on IUCN Red List of Threatened Species. The mean values of the following indices were obtained: H’= 1.1984, DMn= 0.7124, J= 0.6877 and D= 0.3877. Mangrove diversity in Biliran municipality was very low with a highly even distribution of species and uniform distribution of individuals. Since mangal ecosystems in the municipality of Biliran are facing natural and anthropogenic disturbances, the local government unit should prioritize mangrove forest conservation and rehabilitation. *Corresponding Author: Litlen P. Dapar  [email protected] Journal of Biodiversity and Environmental Sciences (JBES) ISSN: 2220-6663 (Print) 2222-3045 (Online) Vol. 22, No. 5, p. 76-86, 2023 http://www.innspub.net
  • 2.
    J. Bio. &Env. Sci. 2023 77 | Dapar et al. Introduction Mangroves ecosystems are mostly composed of halophytic tree and shrub species that are regularly expose to fluctuations in water level, hydrodynamic energy, salinity, nutrient availability, and anoxia (Friess, 2016). Despite thriving in a dynamic and physiologically stressful location, a plethora of coastal and terrestrial fauna are associated with this vegetation including fish, crustaceans, snakes and mammals. In addition to their unique biodiversity value, mangroves are largely important habitats due to some tangible provisioning ecosystem services they provide to the local coastal populations such as timber, charcoal, non-timber forest products and fish/shellfish. The United Nations Environment Programme (2014) further cited that mangrove ecosystem provides millions of people with food, clean water, raw materials and resilience against future climate change impacts including increasing storm intensity and sea level rise. For instance, when super typhoon Haiyan struck the central Philippines, areas with mangrove forests suffered significantly less damage as the trees acted as shield from the strong winds and waves (Ranada, 2014). Faustino et al. (2020) noted that mangrove forests in the Philippines have been continuously dwindling in terms of forest cover and diversity due to anthropogenic activities which include cutting of trees for the production of firewood, charcoal, and building materials, and residential, urban and industrial development, and conversion to agriculture (Maneja, 2006; Bitantos et al., 2017) as well as natural disturbances. In view of these challenges, it is important to conduct baseline studies to give not only a benchmark of an area’s biodiversity but a picture of its overall importance in the landscape (Flora and Fauna International, 2014). A baseline study can highlight areas of importance for biodiversity conservation, identify threats to species and habitats, and help understand how local communities use and value resources. Fortes and Salmo (2017) cited that mangrove studies in the Philippines are initially categorized under seven topics including taxonomy, physiology, economic uses, biogeography, ecology, biodiversity, and conservation and management. However, information on species composition and diversity studies of mangroves from the different parts of the country remains limited and scarce (Baleta and Casalamitao, 2016). Recent local biodiversity studies and vegetational analysis on mangroves have been carried out in Surigao del Norte (Goloran et al., 2020), Camarines Sur (Faustino et al., 2020), Oriental Mindoro (Raganas et al., 2020), Palawan (Dangan-Galon et al., 2016), Camotes island (Lillo et al., 2022), Timaco Mangrove Swamp in Cotabato City (Cano-Mangaoang et al., 2022), Samar island (Mendoza and Alura, 2001), Zamboanga Sibugay (Bitantos et al., 2017), Pangasinan (Rosario et al., 2021), Aurora (Rotaquio et al., 2017), Cagayan Valley (Calicdan et al., 2017), Isabela (Baleta and Casalamitao, 2016), Aklan (Barrientos and Apolonio, 2017), Quezon province (Abantao et al., 2015), and Leyte island (Bobon-Carnice et al., 2021). To date, mangrove studies on the island of Biliran is not documented, particularly in the municipality of Biliran where a large portion of mangrove forest in the village of Sangalang became a wasteland when many mangrove trees and associated species died during the onslaught of tropical depression (TD) Urduja in 2017. Thus, this study was conducted to gather scientific-based data that can serve as a baseline in determining the diversity and conservation status of mangrove species based on the International Union for the Conservation of Nature (IUCN) Red List of Threatened Species. Such baseline can be used in prioritizing areas for conservation and protection of mangal ecosystems in the island, especially with the ongoing threats of both anthropogenic and natural disturbances. Material and methods Establishment of Sampling Plots and Identification of Mangrove Species Five coastal villages with mangrove areas in the municipality of Biliran, namely: Burabod, Busali, Sangalang, Julita, and Villa Enage were selected as study sites based on the preliminary survey (Fig. 1).
  • 3.
    J. Bio. &Env. Sci. 2023 78 | Dapar et al. The village of Bato was excluded due to the dominance of Nypa fruticans Wurmb. in its mangrove area. The methodology followed by Faustino et al. (2020) was modified based on the field conditions. Thus, only a total of 32 quadrats or plots with a size of 10×10 m were established. Inside the plots, each mangrove tree was identified down to the species level using a field guide (Primavera, 2009). The number of individuals per species were counted and recorded on a field notebook. Presence of anthropogenic disturbances whether inside or outside the plots were also noted. Fig. 1. Map of the location of study sites in the municipality of Biliran showing: A) Busali and Burabod; and B) Villa Enage, Sangalang, and Julita. Sources: DENR 8-FLUP Team and Biliran LGU MTWG; Google Maps. Analysis of Data Using the data on the number of individuals for each species, the following indices were computed: 1. Species Richness (Menhinick Index) (DMn) √ where: S = total no. of species observed N = total number of individuals in the sample DMn = Menhinick Index 2. Species Diversity (Shannon-Wiener Index) H’ = ∑ Pi ln Pi where: H’ = Shannon-Wiener Index S = no. of species pi = proportion of individuals of the abundance of the ith species expressed as proportion of total abundance (ni/N) ln= natural logarithm 3. Equitability (Pielou’s Evenness Index) J = H’/ln(S) where: H’ = Shannon-Wiener Index of Diversity S = total number of species ln = natural logarithm J = Pielou’s Evenness Index 4. Species Dominance (Simpson Index) D = ∑ where: n= number of individuals of the ith species N = total number of individuals ∑ = the sum of the calculations D = Simpson Index
  • 4.
    J. Bio. Env. Sci. 2023 79 | Dapar et al. Result and discussion Species Composition of Mangroves A total of 13 mangrove species belonging to 7 families could be found thriving in the coastal villages of Biliran municipality (Table 1). The identified species were Avicennia rumphiana Hallier f., Avicennia marina (Forssk.) Vierh., and Avicennia alba Blume from Avicenniaceae family; Rhizophora apiculata Blume, Rhizophora stylosa Griff., Rhizophora mucronata Lam., Ceriops tagal (Perr.) C. B. Rob., and Bruguiera sp. from Rhizophoraceae family; Sonneratia alba Sm. from Sonneratiaceae family; Exoecaria agallocha L. from Euphorbiaceae family; Scyphiphora hydrophyllacea C. F. Gaertn. from Rubiaceae; Xylocarpus granatum J. Koenig from Meliaceae family; and Brownlowia tersa (L.) Kosterm. from Tiliaceae family. Majority of the mangrove species found in the study sites belonged to Rhizophoraceae family (57.31%), followed by Avicenniaceae family (29.68%) (Fig. 2). Only 0.23% of the mangroves belonged to Meliaceae family. Table 1. Mangrove species that can be found in the municipality of Biliran. Family Name Species Name Local Name Avicenniaceae Avicennia rumphiana Miapi Avicenniaceae Avicennia marina Miapi Avicenniaceae Avicennia alba Miapi Rhizophoraceae Rhizophora apiculata Bakhaw lalaki Rhizophoraceae Rhizophora stylosa Bakhaw bato Rhizophoraceae Rhizophora mucronata Bakhaw babae Rhizophoraceae Ceriops tagal Tangal Rhizophoraceae Bruguiera sp. Pototan Sonneratiaceae Sonneratia alba Pagatpat Euphorbiaceae Exoecaria agallocha Lipata Rubiaceae Scyphiphora hydrophyllacea Nilad Meliaceae Xylocarpus granatum Tabigi Tiliaceae Brownlowia tersa Magaromon Fig. 2. Composition of mangroves based on families. Abundance, Occurrence, and Distribution of Mangrove Species The abundance, occurrence, and distribution of mangrove species in the municipality of Biliran differed based on the study sites (Table 2). A total of 438 individuals of mangrove species were counted in the study sites, in which, R. apiculata Blume was the most abundant (165 individuals) while B. tersa (L.) Kosterm. was the least abundant species (1 individual). The 3 mangrove species, C. tagal (Perr.) C.B. Rob., R. apiculata Blume, and A. marina (Forssk.) Vierh. were found in all of the study sites whereas S. alba Sm. Were also found in 4 study sites, except in Busali. R. stylosa Griff. and X. granatum J. Koenig were seen thriving in Sangalang and Villa Enage while E. agallocha L. were found in both Sangalang and Busali. On the other hand, 4 species including A. rumphiana Hallier f., A. alba Blume, S. hydrophyllacea C. F. Gaertn., and B. tersa (L.) Kosterm. seemed to be limited to Sangalang while R. mucronata Lam. and Bruguiera sp. were seemingly restricted to Julita and Villa Enage, respectively. Table 2. Abundance, occurrence, and distribution of mangroves per study site in the municipality of Biliran. Species Study Site Total Number of Individuals Burabod Busali SangalangJulita Villa Enage A. alba X X 71 X X 73 A. rumphiana X X 10 X X 10 A. marina 20 9 1 6 11 47 R. stylosa X X 1 X 8 9 R. mucronata X X X 2 X 2 R. apiculata 16 6 21 61 61 165 C. tagal 1 9 58 2 2 72 Bruguiera sp. X X X X 3 3 S. alba 3 X 8 13 23 47 E. agallocha X 1 3 X X 4 S. hydrophyllacea X X 3 X X 3 X. granatum X X 1 X 1 2 B. tersa X X 1 X X 1 Total 40 25 178 84 111 438 Note: X= Not present
  • 5.
    J. Bio. Env. Sci. 2023 80 | Dapar et al. Fig. 3. Both natural and anthropogenic disturbances are threatening the existence of A. rumphiana in Sangalang. Diversity of Mangrove Species The species richness (DMn), dominance (D), evenness (J) and diversity (H’) of mangrove species per study site in the municipality of Biliran is shown in Fig. 4. The mean species richness obtained was DMn= 0.7124 and mean species diversity was H’= 1.1984, in which Sangalang recorded both the highest species richness value of DMn = 0.8245 and species diversity value of H’= 1.5390. However, this mean H’ index value could be considered as very low in terms of diversity. On the other hand, the mean equitability index obtained was J’= 0.6877, in which Busali had the highest equitability value of J= 0.8706. This J value indicated a highly even distribution of the mangrove species in the study sites. In terms of dominance, the mean species dominance value obtained was D=0.3877, in which Julita had the highest dominance value of D=0.5575. This D value suggested a uniform distribution of individuals among the mangrove species in the study area. Table 3. Species richness (DMn), dominance (D), equitability (J) and diversity (H’) index of mangrove species per study site in the municipality of Biliran. Index Study Site Total Mean Burabod Busali Sangalang Julita Villa Enage Species Richness 0.6325 0.8000 0.8245 0.5455 0.7593 3.5618 0.7124 Species Diversity 0.9996 1.2070 1.5390 0.8876 1.3590 5.9922 1.1984 Equitability 0.7210 0.8706 0.6420 0.5515 0.6533 3.4384 0.6877 Dominance 0.4163 0.3184 0.2851 0.5575 0.3614 1.9387 0.3877 Conservation Status of Mangrove Species Among the 13 identified mangrove species, A. rumphiana Hallier f. is the only mangrove species listed as Vulnerable (VU) based on IUCN Red List of Threatened Species of 2022 while the rest of the species were either listed as Least Concern (LC) or Not Evaluated (NE) (Table 4). This mangrove species could only be found in Sangalang where both natural and anthropogenic disturbances are threatening the existence of this species (Fig. 4). Large tracts of mangrove areas in this village were decimated due to mudslide and flooding events caused by tropical depression Urduja in 2017. Insect infestation of the mangroves is highly likely because of the presence of many caterpillars. Indications of anthropogenic disturbances were also evident in the site including
  • 6.
    J. Bio. Env. Sci. 2023 81 | Dapar et al. presence of cutting marks in 2 mangrove trees and degrading pieces of metallic fishing net. Table 4. Mangrove species and their ecological status based on IUCN Red List of Threatened Species in the municipality of Biliran. Family Name Species Name Ecological Status Avicenniaceae Avicennia rumphiana Vulnerable (VU) Avicenniaceae Avicennia marina Least concern (LC) Avicenniaceae Avicennia alba Least concern (LC) RhizophoraceaeRhizophora apiculata Least concern (LC) RhizophoraceaeCeriops tagal Least concern (LC) RhizophoraceaeRhizophora stylosa Least concern (LC) RhizophoraceaeRhizophora mucronata Least concern (LC) RhizophoraceaeBruguiera sp. - Sonneratiaceae Sonneratia alba Least concern (LC) Euphorbiaceae Exoecaria agallocha Not evaluated () Rubiaceae Scyphiphora hydrophyllacea Least concern (LC) Meliaceae Xylocarpus granatum Least concern (LC) Tiliaceae Brownlowia tersa Not evaluated (NE) Note: The symbol - means that ecological status could not be determined since it was not identified down to the species level. Discussion Species Composition of Mangroves Noor et al. (2012) cited that species within Rhizophoraceae family are among the most significant and most widely distributed mangal species. Species dominance of Rhizophoraceae family could even reach 90% of the total vegetation, in which optimal growth usually occurs in deeply inundated land and humus-rich soil. Families of Avicenniaceae and Rhizophoraceae often dominate the mangal population in terms of number of species and abundance (Hogarth, 2013). In Indonesia, the Rhizophoraceae family primarily consisting of Bruguiera gymnorrhiza (L.) Lam., R. mucronata Lam., R. apiculata Blume, R. stylosa Griff., and C. tagal (Perr.) C.B. Rob. was found more often than the other families of mangroves (Utina et al., 2019). They have highly developed morphological and physiological adaptations to extreme intertidal environments, and are predisposed with genes which are crucial for increased capability of stress tolerance including defense against salt and oxidative stress, and development of adaptive traits like vivipary (Guo et al., 2017). All Rhizophora taxa are also characterized by large water-buoyant propagules with a remarkable ability for long-distance dispersal (Rabinowitz, 1978). The strong enclosure of its young shoots by conspicuous rounded or flattened stipules and colleter exudates offer structural and mechanical protection, shielding the young shoots of these mangrove plants from their harsh environments (Sheue et al., 2012). Along with Rhizophoraceae family, species from Avicenniaceae family also form the dominant plant communities of mangrove forests (Duke, 1991). As an important member of the mangal formation, all species of this family exhibit adaptations convergent with those of other mangroves such as tolerance of high salt concentrations, excretion of hypersaline solutions on both leaf surfaces via subsessile glandular hairs, xerophytic specializations of leaves, sea-water dispersed viviparous fruits, and soft mud catching hypocotyl of the embryo that allows immediate growth of the seedling (Sanders, 1997). Abundance, Occurrence, and Distribution of Mangrove Species Mangrove species including C. tagal (Perr.) C. B. Rob., R. apiculata Blume, and A. marina (Forssk.) Vierh. were generalist species because they were found in all of the study sites, whereas A. rumphiana Hallier f., A. alba Blume, S. hydrophyllacea C. F. Gaertn., B. tersa (L.) Kosterm., R. mucronata Lam., and Bruguiera sp. were specialist species because they were only found in one study site. Kirsch (2021) cited that generalist species have a wider range of environmental tolerance and utilize a variety of resources by possessing widely applicable features that are not constricted to a narrow function. On the contrary, ecological specialist species have narrowly evolved characteristics that optimize their fitness in their local environment at the cost of vulnerability to disturbance and a high level of dependence on their available niche. It has been shown that habitat heterogeneity tends to favor generalist species temporally and spatially, while specialists benefit from homogeneous habitat conditions (Büchi and Vuilleumier, 2014; Marvier et al., 2004; Devictor et al., 2008; Verberk et al., 2010). Büchi and Vuilleumier (2014) further explained that life-history
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    J. Bio. Env. Sci. 2023 82 | Dapar et al. traits such as niche breadth and dispersal ability, and environmental factors like disturbance, spatial heterogeneity, and autocorrelation could influence the coexistence of specialist and generalist species. Diversity of Mangrove Species Rosario et al. (2021) interpreted H’ index of diversity as very low (1.999), low (2.000-2.499), moderate (2.500-2.999), high (3.000-3.499), or very high (3.500). The very low diversity of mangroves in the municipality of Biliran was comparable to the mangrove forests in Tacloban City, Leyte (Patindol and Casas, 2019), Binmaley, Pangasinan (Rosario et al., 2021), Dumanquillas Bay, Zamboanga Sibugay ((Bitantos et al., 2017), Cancabato Bay, Leyte (Bobon- Carnice et al., 2021), and Mabini, Davao de Oro (Manual et al., 2022). Morris et al. (2014) after Shannon (1948) explained that in a highly diverse system, an unknown individual could belong to any species which often leads to a high uncertainty in predicting its identity. In a less diverse system dominated by one or a few species, it is easier to predict the identity of unknown individuals and there is less uncertainty in the system. Fatonah et al. (2021) emphasized that species evenness values equal to or close to 1 means the species are evenly distributed. It is also categorized as uneven (0.00-0.40), moderately even (0.41-0.60), and highly even (0.61-1.00). Equitability represents the degree to which individuals are split among species with low values indicating that one or a few species dominate, and high values indicating that relatively equal numbers of individuals belong to each species (Morris et al., 2014). Meanwhile, dominance values close to one (1) imply a clumping of individuals in a few species whereas values close to zero (0) mean a more uniform distribution of individuals among the species (Doherty et al., 2011). The dominance has a range value of 0 where all taxa are equally distributed to 1 where one taxon dominates the community completely (Manual et al., 2002). A variety of both biotic and abiotic factors play a role in influencing the diversity of mangrove species and their distributional patterns. Mangroves are forest types consisting of all plants along the coast or river estuary which are affected by tides and interacting with their environment (Irsadi et al., 2019). Duke et al. (1998) stated that numerous factors affect the distribution of mangrove plants including direction of sea currents, presence of land barriers, and species- specific characteristics such as their water-buoyant propagules, establishment success and growth development rate, and tolerance limits and growth responses. Ellison (2021) further explained that mangrove ecosystem diversity and dynamics are influenced by physical factors of temperature, coastal typology, ocean currents and land barriers, wave action and sediment supply, river catchment discharge and sediment yield, and tidal range and inundation frequencies. Factors of gradients and tidal ranges control the lateral extent of mangroves through inundation frequency, and factors influencing accretion rates in the context of relative sea level change can shift or eliminate mangrove extents over time. Conservation Status of Mangrove Species Triest et al. (2021) reported that the IUCN Red List of Threatened Species considered A. rumphiana Hallier f. is a species with vulnerable status because of its patchy distribution, being uncommon in some areas, and declining population. It also thrives in the upper part of the intertidal zone where it is most vulnerable to human activities and habitat destruction. Chan et al. (2022) explained that population trend of this species is decreasing and the mangrove habitat within this species range has declined at least 30% from 1980 to 2005. However, there are no available data to estimate the decline of population as well as no measures have been in placed for the conservation and protection of this species. Conclusion Results revealed 13 mangroves belonging to 7 families including A. rumphiana, A. marina, A. alba, R. apiculata, R. stylosa, R. mucronata, C. tagal, Bruguiera sp., S. alba, E. agallocha, S. hydrophyllacea, X. granatum, and B. tersa. Majority of the mangroves belonged to Rhizophoraceae family.
  • 8.
    J. Bio. Env. Sci. 2023 83 | Dapar et al. R. apiculata was the most abundant while B. tersa was the least abundant species. C. tagal, R. apiculata, and A. marina were found in all of the study sites whereas S. alba. was found in 4 study sites. R. stylosa and X. granatum thrived in Sangalang and Villa Enage while E. agallocha inhabited Sangalang and Busali. A. rumphiana, A. alba, S. hydrophyllacea, and B. tersa were limited to Sangalang while R. mucronata and Bruguiera sp. were restricted to Julita and Villa Enage, respectively. The mean values of the following indices were obtained: H’= 1.1984, DMn= 0.7124, J= 0.6877 and D= 0.3877. Mangrove diversity in Biliran municipality was very low with a highly even distribution of species and uniform distribution of individuals. A. rumphiana was the only mangrove species listed as Vulnerable (VU) based on IUCN Red List of Threatened Species while rests of the species were either listed as Least Concern (LC) or Not Evaluated (NE). Recommendation(S) The mangal forests of Biliran municipality are facing both natural and anthropogenic disturbances. To protect these fragile ecosystems, a multi-sectoral and science-based conservation and rehabilitation programs must be formulated and undertaken. The local government unit of Biliran, Biliran Province State University-Biliran Campus, and People’s Organizations in the municipality of Biliran must work hand-in hand to ensure the sustainability of the programs. Since the diversity of mangrove species in the municipality of Biliran was very low, tree planting activities that take into account zonation patterns of mangrove species and site-species matching principles are also recommended. To capture on-ground status and conditions of mangroves in the entire Biliran island, similar baseline studies must be conducted in the other municipalities, particularly in the island municipality of Maripipi due to the known effects of island biogeography on distributional patterns and diversity of species. Acknowledgements Our heartfelt thanks to Dr. Randy A. Villarin, Dean of the School of Agribusiness and Forest Resource Management, faculty and students of the Department of Forest Science, and the Farmers and Fisherfolks Association (FFA) of Sangalang for their support and assistance in the conduct of this study. References Abantao SC, Apacible TC, Cortez SP, Pereda LT, Yllano OB. 2015. Mangrove species diversity and on-site impact assessment of mangal coastal areas. Expert Opinion on Environmental Biology 4(3), 100-105. DOI:10.4172/2325-9655.1000122. Baleta FN, Casalamitao RSJ. 2016. Species composition, diversity and abundance of mangroves along the estuarine Area of Maligaya, Palanan, Isabela, Philippines. International Journal of Fisheries and Aquatic Studies 4(2), 303-307. Barrientos K, Apolonio JW. 2017. Species diversity and soil carbon sequestration potential of mangrove species at Katunggan It Ibajay (KII) Eco- Park in Aklan, Philippines. PRISM: The Official Research Publication of Negros Oriental State University, Negros Oriental. ISSN: 0119-4607/EISSN: 2546-0390. Available at: https://ssrn.com /abstract= Biliran Provincial MDG Team. 2010. Status Report on the Millennium Development Goals Using CBMS Data. Province of Biliran - National Economic and Development Authority. Available at: http:// www. neda.gov.ph /econreports... /MDGs /... /PR. Bitantos BL, Abucay MD, Dacula JA, Recafort RD. 2017. Mangrove in the grove: diversity, species composition, and habitat in Pamintayan, Dumanquillas Bay, Philippines. Advances in Environmental Science Bioflux 9(3), 183-192. Bobon-Carnice PA, Magayes MR, Gacus EE, Operario EC, Martija MAA. 2021. Aboveground carbon storage and species diversity of mangrove stand in Leyte Island, Philippines. ARADMAN: A Multidisciplinary Research Journal 1(1), 50-69.
  • 9.
    J. Bio. Env. Sci. 2023 84 | Dapar et al. Büchi L, Vuilleumier S. 2014. Coexistence of specialist and generalist species is shaped by dispersal and environmental factors. The American Naturalist 183(5), 612-624. Calicdan MA, Rebancos C, Ancog R, Baguinon N. 2015. Assessment of mangrove flora of Palaui Island Protected Landscape and Seascape (PIPLS) San Vicente, Sta. Ana Cagayan Valley, Philippines. Asian Journal of Conservation Biology 4(1), 15-19. ISSN 2278-7666. Cano-Mangaoang C, Amino ZC, Mastur BB. 2022. Status of mangrove forest in Timaco Mangrove Swamp, Cotabato City, Philippines. Journal of Threatened Taxa 14(11), 22080-22085. DOI: 10.11609 /jott.7826.14.11.22080-22085. Chan EWC, Tangah J, Kezuka M, Chan HT. 2022. Botany, distribution, phytochemistry and bioactivities of mangrove plants VI: Avicennia rumphiana. ISME/GLOMIS Electronic Journal 20(2), 13-16. Dangan-Galon F, Dolorosa RG, Sespeñe JS, Mendoza NI. 2016. Diversity and structural complexity of mangrove forest along Puerto Princesa Bay, Palawan Island, Philippines. Journal of Marine and Island Cultures 5(2), 118-125. Devictor V, Julliard R, Jiguet F. 2008. Distribution of specialist and generalist species along spatial gradients of habitat disturbance and fragmentation. Oikos 117, 507-514. Doherty JH, Harris C, Hartley L. 2011. Calculating Biological Diversity: Teaching Issues and Experiments in Ecology. Ecological Society of America. Available at: https://tiee.esa.org/vol/v7/ experiments /doherty/resources/diversity.doc. Duke N, Duke C, Ball MC, Ellison JC. 1998. Factors Influencing Biodiversity and Distributional Gradients in Mangroves. Global Ecology and Biogeography Letters 7(1), 27-47. Duke NC. 1991. A systematic revision of the mangrove genus Avicennia (Avicenniaceae) Australasia. Australian Systematic Botany 4, 299- 324. DOI: 10.1071/SB9910299. Ellison JC. 2021. Factors Influencing Mangrove Ecosystems. In: Rastogi RP, Phulwaria M, Gupta DK, Ed. Mangroves: Ecology, Biodiversity and Management. New Delhi, India: Springer p. 97-115. Fatona S, Hamidy R, Mulyadi A, Friyeldi E. 2021. Floristic composition and stand structure of mangrove forests with varying vegetation conditions in Sungai Apit, Siak, Riau, Indonesia. Biodiversitas 22, 3972-3983. DOI: 10.13057/biodiv /d220945. Faustino AZ, Madela HL, Castor RG, Muroda AP, Chavez MNP. 2020. Community mapping and vegetational analysis of the mangrove forest in Calabanga, San Miguel Bay, Philippines. E3S Web of Conferences 147(2), 02017. Flora and Fauna International. 2017. Biodiversity Baselines for Development and Conservation. Available at: https://www.faunaflora. org/app/uploads/2017/12/FFI2014_Biodiversity- baselines -for-development-and-conservation.pdf. Fortes MD, Salmo S III. 2017. Technical presentations. Status of mangrove research and management in the Philippines: Challenges and opportunities. Ateneo Journals Online 2(2), 50-60. Friess DA. 2016. Quick guide to mangrove forests. Current Biology 26, R739-R755. Goloran AB, Demetillo MT, Betco GL. 2020. Mangrove assessment and diversity in coastal area of Barangay Cagdianao, Claver, Surigao del Norte, Philippines. International Journal of Environmental Sciences and Natural Resources 26(3), 556-188. Gregorio N, Herbohn J, Tripoli R, Pasa A. 2020. A Local Initiative to Achieve Global Forest and Landscape Restoration Challenge—Lessons Learned from a Community-Based Forest Restoration Project in Biliran Province, Philippines. Forests 11(4), 475.
  • 10.
    J. Bio. Env. Sci. 2023 85 | Dapar et al. Guo W, Wu H, Zhang Z, Yang C, Hu L, Shi X, Jian S, Shi S, Huang Y. 2017. Comparative analysis of transcriptomes in Rhizophoraceae provides insights into the origin and adaptive evolution of mangrove plants in intertidal environments. Frontiers in Plant Science Section Evolutionary and Population Genetics 8, 00795. Hogarth PJ. 2013. Mangrove Ecosystems: Rhizophoraceae. In: Levin Sa, 2nd Ed. Encyclopedia of Biodiversity: Academic Press, p: 10-22. Irsadi A, Anggoro S, Soeprobowati TR. 2019. Environmental Factors Supporting Mangrove Ecosystem in Semarang-Demak Coastal Area. E3S Web of Conferences 125, 01021. IUCN. 2022. IUCN Red List of Threatened Species. Available at https://www.iucnredlist.org. Kirsch AN. 2021. Defining plant ecological specialists and generalists: Building a framework for identification and classification [Master’s thesis, Minnesota State University, Mankato]. Cornerstone: A Collection of Scholarly and Creative Works for Minnesota State University, Mankato. Available at: https://cornerstone.lib. mnsu.edu/etds/1175. Lillo EP, Malaki AB, Alcazar SMT, Rosales R, Redoblado BR, Diaz JLB, Pantinople EM, Nuevo RU. 2022. Composition and diversity of Mangrove species in Camotes Island, Cebu, Philippines. Journal of Marine and Island Cultures 11(1), 2212-6821. DOI: 10.21463/jmic. 2022.11.1.11. Maneja RH. 2006. Analysis of the responses of mangrove ecosystems in the Philippines to climate change. Agusan River Basin Mangrove Wildlife Conservation Network Website. Available at: http://www.freewebs.com/arbm wcnetwork/. Manual AMB, Gabato NAS, Jetuya QB, Alimbon JA. 2022. Floristic composition, structure, and diversity of mangroves in the coastal areas of Mabini, Davao de Oro, Philippines. Biodiversitas 23(9), 4887-4893. DOI: 10.13057/biodiv/d230958. Marvier M, Kareiva P, Neubert MG. 2004. Habitat destruction, fragmentation, and disturbance promote invasion by habitat generalists in a multispecies metapopulation. Risk Analysis 24, 869- 878. Mendoza AB, Alura DP. 2001. Mangrove Structure on the Eastern Coast of Samar Island, Philippines. In: Stott DE, Mohtar RH, Steinhardt GC, Ed. Sustaining the Global Farm. Indiana USA: Purdue University p. 423-425. Morris EK, Caruso T, Buscot F, Fischer M, Hancock C, Maier TS, Meiners T, Muller C, Obermaier E, Prati D, Socher SA, Sonnemann I, Waschke N, Wubet T, Wurst S, Rillig MC. 2014. Choosing and using diversity indices: insights for ecological applications from the German Biodiversity Exploratories. Ecology and Evolution 4(18), 3514- 3524. DOI: 10.1002/ece3.1155. Noor YR, Khazali M, Suryadiputra INN. 2012. The Third Printing Guide for Mangrove Indonesia in 2012. Wetlands International Indonesia Programme. Bogor, Indonesia. Patindol T, Casas JE. 2019. Species diversity and composition of mangroves in Tacloban City Philippines. Annals of Tropical Research 41, 67-75. DOI:10.32945/atr4126.2019. PhilAtlas. 2023. Biliran, Biliran Profile - PhilAtlas. Available at: https://www.philatlas.com/visayas/ r08/biliran/biliran.html Primavera JH. 2009. Field Guide to Philippine Mangroves. Philippine Tropical Forest Conservation Foundation, Inc. and Zoological Society of London. Rabinowitz D. 1978. Dispersal properties of mangrove propagules. Biotropica 10, 47-57. Raganas AFM, Magcale-Macandog DB. 2020. Physicochemical factors influencing zonation patterns, niche width and tolerances of dominant mangroves in southern Oriental Mindoro, Philippines. Ocean Life 4(2), 51-62.
  • 11.
    J. Bio. Env. Sci. 2023 86 | Dapar et al. Ranada P. 2014. The importance of mangrove forests. The Manila Times. Available at: https://www./manilatimes.net/importance- mangrove-forests/14404 5/. Rosario GR, dela Peña RV, de Guzman R, Abalos RS, Tamayo E. 2021. Species composition and diversity of mangroves in the riverbanks of Barangay Basing, Binmaley, Pangasinan. Journal of Natural and Allied Sciences 5(1), 51-59. Rotaquio EL, Nakagoshi N, Rotaquio RL. 2007. Species composition of mangrove forests in Aurora, Philippines: A special reference to Kandelia candel (L.) Druce. Journal of International Development and Cooperation 13(1), 61-78. Sanders RW. 1997. The Avicenniaceae in the Southeastern United States. Harvard Papers in Botany 1(10), 81-92. Sheue CR, Chen Y, Yang Y. 2012. Stipules and colleters of the mangrove Rhizophoraceae: morphology, structure and comparative significance. Botanical Studies 53, 243-254. Triest L, Del Socorro A, Gado VJ, Mazo AM, Sierens T. 2021. Avicennia genetic diversity andfine-scaled structure influenced by coastal proximity of mangrove fragments. Frontiers in Marine Science Section Global Change and the Future Ocean 8, 643982. DOI: 10.3389/fmars.2021.643982. United Nations Environment Programme. 2014. The Importance of Mangroves to People: A Call to Action. In: van Bochove J, Sullivan E, Nakamura T, Ed. United Nations Environment Programme World Conservation Monitoring Centre, Cambridge. Utina R, Katili AS, Lapolo N, Dangkua T. 2019. Short Communication: The composition of mangrove species in coastal area of Banggai District, Central Sulawesi, Indonesia. Biodiversitas 20(3), 840-846. DOI: 10.13057/biodiv/d200 330. Verberk W, van der Velde G, Esselin H. 2010. Explaining abundance-occupancy relationships in specialists and generalists: a case study on aquatic macroinvertebrates in standing waters. Journal of Animal Ecology 79, 589-601.