Journal of Marine and Island Cultures

Open Access Journal — ISSN 2212-6821

Composition and diversity of Mangrove species in Camotes Island, Cebu, Philippines

Edgardo P. Lillo Cebu Technological University, Cebu, Philippines. Forest Biological Sciences, College of Forestry and Natural Resources, University of the Philippines Los Baños, Philippines.

Archiebald B. Malaki Cebu Technological University, Cebu, Philippines. Forest Biological Sciences, College of Forestry and Natural Resources, University of the Philippines Los Baños, Philippines. School of Environmental Science and Management.

Steve Michael T. Alcazar Cebu Technological University, Cebu, Philippines. Forest Biological Sciences, College of Forestry and Natural Resources, University of the Philippines Los Baños, Philippines. School of Environmental Science and Management.

Raamah Rosales Cebu Technological University, Cebu, Philippines.

Bernardo R. Redoblado Cebu Technological University, Cebu, Philippines.

John Lou B. Diaz Cebu Technological University, Cebu, Philippines.

Erwin M. Pantinople Cebu Technological University, Cebu, Philippines.

Ritche U. Nuevo Cebu Technological University, Cebu, Philippines.

Received 27 February 2022, Accepted 14 March 2022, Available online 30 June 2022 10.21463/jmic.2022.11.1.11

Abstract

Mangrove forests are one of the world’s most threatened tropical ecosystems. The study aimed of assessing the composition and diversity of Mangrove species in Camotes Island, Philippines, as basis for its conservation and protection. A Belt in line transect method was used, with a minimum length of 1000m and maximum of 2000m along landward, middle, and seaward at an interval of 100m. Quadrat of 10 x 10m were established within the transect line at an interval of 250m. All the plant species within the quadrats were identified and measured.

A total of 42 mangrove species were recorded in the island, representing 31 true mangrove species, and 11 mangrove associates. Two species were identified as Endangered Pemphis acidula J.R.Forst. & G.Forst and Camptostemon philippinense (S.Vidal) Becc, with a relative value of high species diversity (H’ = 3.0107). Camotes Island were dominated by the species of Sonneratia alba Sm, Avicennia marina (Forssk.) Vierh Avicennia rumphiana Hallier f, Rhizophora apiculata Blume, and Rhizophora stylosa Griff. Jaccard’s and Sorensen dissimilarity matrix prove that the mangrove species of Camotes Island were forming three cluster.

Conservation effort and Information Education Campaign were needed by the Local Government Units, to protect the high mangrove species diversity of Camotes Island.

Keywords

Composition, diversity, Pilar, Poro, San Francisco, Tudela

Introduction

Mangrove forests are one of the world’s most threatened tropical ecosystems, and in fact 11 true mangrove species are already in the IUCN Red List (Polidoro et al., 2010). As reiterated by Giri et al. (2010), Mangrove forest throughout the world has declined from 18.8 million hectares in 1980 to 15.2 million hectares in 2005. Based on the record of the Food and Agricultural Organization of the United Nations (FAO-UN, 2015) Asia has the most extensive mangrove forest cover, but with the most serious deforestation rates. In Thailand, mangrove forest is already fragmented due to the combined effect of natural disasters and anthropogenic disturbances (Doydee and Buot, 2010).

In the Philippines the rate of losing mangroves is up to 50% (Maritime Review, 2017). As a result, more number of mangrove forest are on the brink of complete collapse (Gevaña, Pulhin, & Tapia, 2019). Based on the record of IUCN, mangrove species in the Philippines are in danger of extinction due to coastal development, climate change, logging, industry, settlements, and agriculture (Maritime Review, 2017). In Cebu Island, anthropogenic activities were also the culprit of mangrove destruction. Coastal inhabitant uses mangrove tree species for crafting poles, fencing, forage, and house construction, as well as for fuel wood (Lillo and Buot, 2016). Mangrove forest also serve as potential sources of livelihood that can provide incentives to coastal communities (Camacho et al., 2011).

The Camotes Island Mangrove Swamp Forest Reserve is declared as protected area under Proclamation No. 2152, s. 1981. The declaration as protected area cover the coastlines of Camotes Island, which serve as a vital defense against the impacts of climate change.  Mangroves are important and valuable, especially on their buffering capacity against storm surge, tsunami, and flooding (Macintosh, 2010; Garcia, Malabrigo & Gevaña, 2014; Gevaña, Camacho, & Pulhin, 2018). Majority of the inhabitants of Camotes Island are residing within 60 km from the coastal zones, making them exposed to natural disasters (PSA, 2017).

Camacho et al. (2011) emphasizing also that mangrove forest plays an important role in Carbon sequestration. Based on the study of Aksornkoae & Kato (2011), a 40-year-old mangrove plantation sequesters 370.7 tons of Carbon per hectare, then a 15-year-old plantation sequesters 208.5 tons of Carbon per hectare. While a 20-year-old plantation sequesters 149.5 tons of Carbon per hectare, and a natural stand sequesters 145.6 tons of Carbon per hectare, lower as compared to established plantation. In addition, mangrove plantation establishment was also driven by the increasing demand for fuelwood, poles, charcoal and woodchips, as well as on their ecological ecosystem functions (Aksornkoae & Kato, 2011).

In the Philippines the target area for reforestation totals to 1.5 million hectares including mangroves to be planted by 1.5 billion trees of combined forest species and fruit trees, with a total budget of 5 billion pesos for a period of six years (DENR-NGP Website). However, despite this reforestation and afforestation effort of the government, still forest ecosystems experience a poor ratio between forest loss to forest gain (3.6:1 from 2000–2010 period) (Hansen et al., 2013). Planting efforts implemented were unsuccessful due to the lack of science-based approach guidelines (López-Portillo et al., 2017). In this situation, there is an urgent need for enhancing our silvicultural knowledge about mangroves, as the key to increase the effectiveness and efficiency of rehabilitation (Thompson, Clubbe, Primavera, Curnick, and Koldewey, 2014).

Philippines serve as habitat to 39 true mangrove species (Sinfuego and Bout, 2014). In Palawan Island almost all Mangrove ecosystems in each Municipalities were documented. Palawan Island has 23 true mangrove species, with species richness ranges from 8 to 17 per Municipality (Dangan-Galon et al., 2016). In Cebu Island information on mangrove species in terms of its composition and diversity were still in adequate. The latest available reference was in Argao, Cebu with 22 species of true mangrove (Lillo and Buot, 2016), and nothing in Camotes Island in any scientific journals.

Knowing the exact composition of mangroves species in Camotes Island was an important prerequisite in understanding its ecology and ecosystem functioning. The information of the mangrove species serve as an important input to the conservation of all marine biodiversity in the island (Lillo and Buot, 2016). Sustainability of natural resources was always intimately linked to ecology. The study aimed of assessing the composition and diversity of Mangrove species in Camotes Island, Philippines, as basis for its conservation and protection.

Methodology

Study area

Camotes Island is found off the north eastern coast of the Island of Cebu, and lies at a coordinates of 10˚37′ to 10º43′10″N, and 124º24′40″ to 124º29′4″E (Figure 1). Camotes Island comprises three major Islands namely; Pacijan, Poro and Ponson. Pacijan Island is entirely within the political jurisdictions of the Municipality of San Francisco (Figure 1). While the whole Island of Ponson belong to the Municipality of Pilar. Then the Municipalities of Poro and Tudela are located on Poro Island (Figure 1; Tanduyan et al., 2013).

Pacijan Island is characterized as grassy with muddy substrates, dominated by Rhizophora, Avicennia, and Sonneratia species. Poro Island is characterized as muddy with rocky substrates, dominated also by Rhizophora, Avicennia, and Sonneratia species. While Ponson Island is characterized as sandy with muddy substrates, dominated by Avicennia, and Sonneratia species (Figure 2; Tanduyan et al., 2013). Mangrove forest is found intact in the coastal areas of Camotes Island.

Location of the different study sites in Camotes Island. A: Location of the different sampling sites. B: Map showing the study site in Cebu Island. C: Map showing the study site in the Philippines (GIS generated, Google Earth map).
Mangrove vegetation type of the four sampling sites in Camotes Island. A,B: Tudela sampling site. C,D,E: San Francisco sampling site. F,G,J,K: Poro sampling site. H,I: Pilar sampling site. Photo by John Lou B. Diaz.

Methods of Gathering the data

A Belt in line transect method was used in the assessment of mangrove species in the site. Three line transects with a minimum length of 1000m and a maximum of 2000m were established (landward, middle, and seaward) in each sampling sites at an interval of 100m. Quadrats of 10 x 10m dimension were then established within the line transect, at an interval of 250m, to a total of 108 plots/quadrats covering all sampling sites.

All the plant species within the quadrats were recorded and identified following the nomenclature of Primavera and Sadaba (2012). The sample specimens was verified also from manuals, herbarium, Co-digital flora of the Philippines, and online literature for accurate identification of the species. Conservation status of the species were based on Department of Environment and Natural Resources Red list of threatened species (DENR-DAO, 2017-11), as well as on IUCN red list (IUCN, 2021-2).

Trees with diameter of 10cm and above were measured in terms of their diameter breast height (DBH) in centimeter (cm), and total height in meter (m). The measurement of DBH was done with the use of diameter tape for larger trees, and tree caliper for smaller trees. For the total height of the trees, the measurement was made by using an Abney hand level. Basal area (m2) computation for the relative dominance computation was based on DENR formula (Basal Area = 0.7854 D2).

Human-related disturbances to mangrove forest were assessed through actual observation by the researchers. Disturbances observed were verified using the Focused Group Discussion (FGD), and the Key Informant Interview (KII) to the coastal residents in the area.

Data Analysis

Diversity of species. Species diversity were computed and interpreted by using the Shannon, and Simpson Diversity Index. The Multi-Variant Statistical Package (MVSP) software was used to compute the Shannon (H’) and Simpson Diversity Index.

Species Density, Dominance, Frequency, and Importance Value Index (IVI). All recorded data was stored in a Microsoft Excel database and analyzed quantitatively by using Microsoft Excel statistics. Vegetation analysis was performed using the formula of Density, Relative Density, Dominance based on Basal Area, Relative Dominance, Frequency, Relative Frequency, and Importance Value Index (IVI). The ecological importance of each species in relation to the total forest community was calculated by summing its Relative Density, Relative Dominance, and Relative Frequency.

Clustering of native tree species community. Differences in mangrove species composition between sites were assessed with floristic dissimilarity matrices in terms of presence/absence (PRAB) and species abundance (ABU) data criteria. Clustering analysis of mangrove species community and composition were determined using the Jaccard’s matrix, and Sorensen dissimilarity matrix through the MVSP software.

Result and Discussion

Species composition

A total of 42 mangrove species recorded in Camotes Island. Out of 42 species, 31 were categorized as true mangrove, and 11 were mangrove associates (Table 1; Figure 3, 4, and 5). The 31 true mangrove species were classified into 13 families and 17 genera (Table 1; Figure 3, 4, and 5). Of the 31 true mangrove species, 27 were recorded in Poro, 26 in Pilar, and 25 for both Tudela and San Francisco sampling sites (Table 1). Camptostemon philippinense (S.Vidal) Becc species was one of the identified threatened species in the island, recorded only in Poro and Pilar sampling sites,  together with Scyphiphora hydrophylacea C.F.Gaertn and Avicennia alba Blume making them more diverse as compared to other sampling sites. The 11 mangrove associate species were recorded in all sampling sites. Rhizopohoraceae was the most recorded Family, and Rhizophora was the most dominant genus.  The dominant species was Sonneratia alba Sm and recorded in almost all sampling sites. Sonneratia alba Sm species was recorded in the seaward side of all the sampling sites. The result of the study compliment to the findings of Reef and Lovelock (2014), that Sonneratia alba Sm together with Rhizophora apiculata and Avicennia marina are the species that grow in ecotypes with medium to higher salinities such as in estuarine and seaward zones.

Mangrove biologists and experts classify mangrove plants into true mangrove and mangrove associates species. True mangrove limited only to the species that thrive in mangrove habitat, while mangrove associates species distributed in a terrestrial habitat, but found also occurring in the mangrove ecosystem (Polidoro et al., 2010).

The recorded 31 true mangrove species in Camotes Island constituted to 79.5% of the 39 true mangrove species recorded in the Philippines (Sinfuego and Bout, 2014). The result was also higher as compared to both Palawan Island with 23 true mangrove species (Dangan-Galon, et al. 2016), and Dinagat Island with 10 species,  8 families and 9 genera (Lillo and Fernando, 2017). The result implies that Camotes Island serve as a home or habitat to a diverse mangrove species.

Composition and Distribution of Mangrove species in different sampling sites of Camotes Island
Scientific name Family name Sampling sites
San Francisco Poro Tudela Pilar
True Mangrove Species
Acanthus ebracteatus Vahl Acanthaceae / / /
Acanthus volubilis Wall Acanthaceae /
Aegiceras corniculatum (L.) Blanco Primulaceae / / /
Aegiceras floridum Roem. & Schult Primulaceae / / / /
Avicennia alba Blume Acanthaceae / /
Avicennia marina (Forssk.) Vierh Acanthaceae / / / /
Avicennia officinalis L. Acanthaceae / / / /
Avicennia rumphiana Hallier f. Acanthaceae / / / /
Bruguiera cylindrica (L.) Blume Rhizophoraceae / / / /
Bruguiera gymnorhiza (L.) Savigny in Lam Rhizophoraceae / / / /
Bruguiera parviflora (Roxb.) Wight & Arn. ex Griff Rhizophoraceae / /
Bruguiera sexangula (Lour.) Poir Rhizophoraceae / /
Camptostemon philippinense (S.Vidal) Becc Bombacaceae / /
Ceriops tagal (Perr.) C.B.Rob Rhizophoraceae / / / /
Ceriops zippeliana Blume Rhizophoraceae / / / /
Excoecaria agallocha L., Syst Euphorbiaceae / / / /
Heritiera littoralisDryand. inAiton Sterculiaceae / / / /
Lumnitzera littorea (Jack) Voigt Combretaceae / /
Lumnitzera racemosa Willd Combretaceae / / / /
Nypa fruticans Wurmb Arecaceae / / / /
Osbornia octodonta F. Muell. Myrtaceae / / / /
Pemphis acidula J.R.Forst. & G.Forst Lythraceae / / /
Rhizophora apiculata Blume Rhizophoraceae / / / /
Rhizophora lamarckii Montrouz Rhizophoraceae / / / /
Rhizophora mucronata Poir. Rhizophoraceae / / / /
Rhizophora stylosa Griff. Rhizophoraceae / / / /
Scyphiphora hydrophylacea C.F.Gaertn Rubiaceae / /
Sonneratia alba Sm. Lythraceae / / / /
Xylocarpus granatum Koen Meliaceae / / / /
Xylocarpus moluccensis (Lam.) M.Roem Meliaceae / / / /
Acrostichum speciosum Willd Pteridaceae /
Sub-Total 25 27 25 26
Mangrove associate species
Hoya sp. Apocynaceae / / / /
Terminalia catappa Linn Combretaceae / / / /
Glochidion littorale Blume Phyllanthaceae / / / /
Breynia vitis-idaea (Burm.f.) C.E.C..Fischer Phyllanthaceae / / / /
Abrus precatorius Linn. Fabaceae / / / /
Albizia retusa Benth. Fabaceae / / / /
Caesalpinia crista Linn. Fabaceae / / / /
Derris trifoliate Lour. Fabaceae / / / /
Flagellaria indica Linn. Flagellariaceae / / / /
Talipariti tiliaceum (Linn.) Fryxell Malvaceae / / / /
Morinda citrifolia Linn Rubiaceae / / / /
Sub-Total 11 11 11 11
Grand total 36 38 36 37
Mangrove species found in Camotes Island. A, B: Acanthus ebracteatus Vahl. C,D: Acanthus volubilis Wall. E: Aegiceras corniculatum (L.) Blanco. F: Aegiceras floridum Roem. & Schult. G: Acrostichum speciosum Willd. H: Avicennia alba Blume. I,J: Avicennia marina (Forssk.) Vierh. K: Avicennia officinalis L. L, M: Avicennia rumphiana Hallier f. Photo by John Lou B. Diaz.
Mangrove species found in Camotes Island. A: Bruguiera cylindrica (L.) Blume. B: Bruguiera gymnorhiza (L.) Savigny in Lam. C: Bruguiera parviflora (Roxb.) Wight & Am. ex Griff. D: Bruguiera sexangula (Lour.) Poir. E: Camptostemon philippinense (S.Vidal) Becc. F: Ceriops tagal (Perr.) C.B.Rob. G: Ceriops zippeliana Blume. H: Excoecaria agallocha L., Syst. I: Lumnitzera littorea (Jack) Voigt. J: Lumnitzera racemosa Willd. K: Nypa fruticans Wurmb. L: Osbornia octodonta F. Muell. Photo by John Lou B. Diaz.
Mangrove species found in Camotes Island. A: Pemphis acidula J.R.Forst. & G.Forst. B: Heritiera littoralis Dryand in Aiton. C: Sonneratia alba Sm. D: Rhizophora lamarckii Montrouz. E: Rhizophora apiculata Blume. F: Rhizophora mucronata Poir. G: Rhizophora stylosa Griff. H: Scyphiphora hydrophylacea C.F.Gaertn. I: Xylocarpus granatum Koen. J: Xylocarpus moluccensis (Lam.) M.Roem. Photo by John Lou B. Diaz.

Diversity of species

Based from the computed diversity index by Shannon, Camotes Island has a species diversity of H’=3.0107 (Figure 6), with a relative value of high species diversity (MacDonald 2003). The result of the study compliment with the total number of true mangrove species identified in the island with 31 (Table 1).

Among the sampling sites Poro has the highest in terms of computed diversity value of H’=3.111, followed by Pilar with a computed diversity value of H’=3.027 (Figure 6).  Both Poro and Pilar sampling sites have a relative value of high species diversity (MacDonald, 2003).  The result compliment to the number of identified true mangrove species in both sampling site (Table 1).

San Francisco and Tudela sampling sites both have a computed diversity value of H’=2.9 (Figure 6).  The sampling sites have a relative value of moderately high species diversity (MacDonald, 2003). The result compliment to the number of identified true mangrove species in both sampling sites with lower in number as compared to Poro and Pilar (Table 1).

In Simpson’s diversity index, all the sampling sites have a relative value of high species diversity (Figure 6). The result of the study implies that the mangrove forest of Camotes Island was still stable and productive. Lillo et al. (2019) emphasized that Species diversity of a certain community attributed to its stability, productivity, and trophic structure. An area with high species diversity results to a more stable and productive ecosystem.

However, as observed in the different sampling sites, anthropogenic activities were existing, and causing damage to mangrove forest, as well as threaten the mangrove species. This anthropogenic activities include illegal cutting, and according to the coastal communities interviewed, they used it for fuel wood production and for charcoal making. Other activities include gathering of leaves and branches for forage, improper disposal of garbage, and debarking of mangrove trees for tan bark production, as well as reclamation of the coastal areas for community and industrial development.

The uncontrolled anthropogenic activities threaten the stability and productivity of the whole Camotes Island mangrove forest. The different Local Government Units in the area must strictly implement the policy of protecting the mangrove species, since the whole Camotes Island was declared as protected area under Proclamation No. 2152, s. 1981.

Diversity indices of Mangrove species in different sampling sites of Camotes Island

Species Density, Dominance, Frequency and Importance value Index (IVI)

The mangrove species with higher in Importance Value Index (IVI) in Camotes Island was Sonneratia alba Sm. (39.17%) (Table 2). The species was the most dominant in terms of diameter, richness, and density in all sampling sites. Based on actual measurement the species reached a maximum diameter of 80cm and total height of 15m. Saplings and wildlings of the species were also abundant in the forest floor in all sampling sites. Identification of the most dominant mangrove species in a particular ecotype provide insights as to what species could be used for the future rehabilitation programs in a certain mangrove ecosystems (Raganas and Magcale-Macandog, 2020).

Other mangrove species with higher Importance Value Index were Avicennia marina (Forssk.) Vierh (26.13%), Avicennia rumphiana Hallier f, ( 24.57%), Rhizophora apiculata Blume, (23.05%),  Rhizophora stylosa Griff., (15.82%),  Avicennia officinalis L. (12.93%), Ceriops zippeliana Blume, (11.48%), and Xylocarpus granatum Koen. (10.15%). The species were dominant in terms of frequency. However, they have a smaller in diameter as compared to Sonneratia alba Sm. The diameter of the trees ranges from 10–40cm, and total height ranges from 8–15m.

In Tudela, Poro, and San Francisco sampling sites Sonneratia alba Sm was also considered as the species with higher Importance Value Index (Table 2; Figure 2). The species was also dominant in terms of diameter, frequency, and density. Other dominant species were Avicennia marina (Forssk.) Vierh, Rhizophora apiculata Blume, Rhizophora stylosa Griff,  Ceriops zippeliana Blume, Xylocarpus granatum Koen, and Avicennia rumphiana Hallier f. (Table 2).

However, in Pilar sampling site, Rhizophora apiculata Blume was considered as the species with higher Importance Value Index (Table 2). The species was dominant in terms of frequency in all sampling plots. The species has a diameter ranges from 10–40 cm, smaller as compared to Sonneratia alba Sm. The total height ranges from 10–15m, similar to Sonneratia alba Sm. Other dominant species were Avicennia marina (Forssk.) Vierh, Sonneratia alba Sm., Rhizophora stylosa Griff, Ceriops zippeliana Blume, Avicennia rumphiana Hallier f, and Rhizophora mucronata Poir. (Table 2). The forest floor of the mangrove forest was also dominated by the seedlings and saplings of the species of Rhizophora apiculata Blume, Rhizophora mucronata Lam, Rhizophora stylosa Griff., Sonneratia alba Sm, and Avicennia marina (Forssk.) Vierh. Rhizophora mucronata Poir was also dominant in Poro and San Francisco sampling sites. But the species was not dominant in Tudela sampling site.

The result of the study is similar with Palawan Island mangrove forest which are dominated by the species of Lumnitzera littorea, Rhizophora apiculata, Rhizophora mucronata, Rhizophora stylosa, Scyphiphora hydrophyllacea, and Sonneratia alba (Dangan-Galon et al., 2016). Similar species are also found dominant in Dinagat Island mangrove forest (Lillo and Fernando, 2017). Das et al. (2019) emphasizing that the distribution pattern of the species have been linked with the Salinity, sulfides, nutrients, sedimentation, soil texture, and nutrients of a certain mangrove  ecosystem.

Relative Density, Relative Dominance, Relative Frequency, and Importance Value Index (IVI) of Mangrove species in different sampling sites
Species Sampling sites Rel. Den. Rel. Dom. Rel. Freq. IVI
Pilar Poro San Fran Tudela
Sonneratia alba Sm. 183 193 138 161 26.29 8.29 4.60 39.17
Avicennia marina (Forssk.) Vierh 186 105 77 96 18.07 3.46 4.60 26.13
Avicennia rumphiana Hallier f 39 17 12 17 3.31 16.67 4.60 24.57
Rhizophora apiculata Blume 207 77 107 45 16.98 1.48 4.60 23.05
Rhizophora stylosa Griff. 99 31 55 83 10.44 0.78 4.60 15.82
Avicennia officinalis L. 13 4 0 0 0.66 9.97 2.30 12.93
Ceriops zippeliana Blume 65 47 20 30 6.31 0.57 4.60 11.48
Xylocarpus granatum Koen 3 15 1 21 1.56 4.00 4.60 10.15
Avicennia alba Blume 2 0 0 0 0.08 5.11 4.60 9.79
Heritiera littoralis Aiton 0 2 0 0 0.08 5.11 4.60 9.79
Rhizophora mucronata Poir. 37 13 11 4 2.53 0.97 4.60 8.10
Excoecaria agallocha L. 5 5 3 16 1.13 2.36 4.60 8.08
Bruguiera cylindrica (L.) Blume 7 6 7 18 1.48 1.99 4.60 8.06
Xylocarpus rumphii (Kostel.) Mabb 4 13 6 10 1.29 2.16 4.60 8.05
Bruguiera sexangula (Lour.) Poir 0 0 0 17 0.66 6.14 1.15 7.95
Ceriops tagal (Perr.) C.B.Rob 7 19 18 6 1.95 0.93 4.60 7.48
Rhizophora lamarckii Montrouz 15 13 7 5 1.56 0.91 4.60 7.07
Bruguiera gymnorhiza (L.) Savigny in Lam 4 7 3 1 0.58 1.28 4.60 6.46
Lumnitzera racemosa Willd 1 3 7 8 0.74 0.81 4.60 6.15
Osbornia octodonta F. Muell. 1 17 0 10 1.09 1.05 3.45 5.59
Aegiceras floridum Roem. & Schult 12 9 0 6 1.05 0.99 3.45 5.49
Aegiceras corniculatum (L.) Blanco 0 7 1 2 0.39 1.60 3.45 5.44
Camptostemon philippinense (S.Vidal) Becc 5 3 0 0 0.31 1.84 2.30 4.45
Pemphis acidula J.R.Forst. & G.Forst 0 10 0 3 0.51 1.63 2.30 4.43
Bruguiera parviflora (Roxb.) Wight & Arn. ex Griff 1 0 1 0 0.08 1.34 2.30 3.71
Scyphiphora hydrophylacea C.F.Gaertn 1 3 0 0 0.16 1.22 2.30 3.68
Lumnitzera littorea (Jack) Voigt 0 0 0 18 0.70 1.63 1.15 3.49
Prosopis juliflora (Sw.) DC 0 0 1 0 0.04 1.71 1.15 2.90

Clustering of Mangrove species (Jaccard’s, and Sorensen Dissimilarity Matrix)

Clustering analysis of the Mangrove species in Camotes Island by Jaccard’s dissimilarity matrix shows that all the plots sampled were forming into three clusters/groups correspondingly (Figure 7). The four sampling sites from Camotes Island proved to have distinctive mangrove species association, hence grouping them together into three distinct clusters. Tudela and Poro sampling sites formed as one group, while San Francisco sampling site formed as one cluster distinct from other sampling sites. Pilar sampling site also formed as one cluster similar to San Francisco. The species composition of the site was distinct from other sampling sites.

The Sorensen dissimilarity matrix shows that all the plots sampled were forming into three clusters/groups similar result in Jaccard’s (Figure 7 and 8). Both the Jaccard’s and Sorensen dissimilarity matrix prove that the mangrove species of Camotes Island were forming three cluster. Wherein the species in San Francisco form as one cluster, similar with Pilar sampling site. While Poro and Tudela mangrove species found to be similar from each other, together forming as one cluster (Figure 7 and 8).

The mangrove species in San Francisco sampling site formed as one cluster because it differ in environmental condition particularly on its substrate from the other sampling sites. Similar situation with Pilar sampling sites. The mangrove species in Poro and Tudela sampling sites was more likely similar from each other, forming as one cluster together because they have similar substrate (Tanduyan et al., 2013).

The result of the study compliment with the geographical location of the different major islands of Camotes Island (Figure 1). The results were also supported by Raganas and Magcale-Macandog (2020) that the differences in the mangrove environmental conditions can result in the dominance of a particular species leading to their habitat differentiation.

Dendrogram of the four sites per Jaccard similarity coefficient and clustering using the Unweighted Pair Group Method with Arithmetic mean (UPGMA) showing three cluster of mangrove species in Camotes Island.
Dendrogram of the four sites per Sorensen similarity coefficient and clustering using the Unweighted Pair Group Method with Arithmetic mean (UPGMA) showing three cluster of mangrove species in Camotes Island.

Conservation Status of the species

Of the 31 true mangrove species, two were identified as threatened and categorized as Endangered species under DENR national listing (DAO, 2017-11).  The species include Pemphis acidula J.R.Forst. & G.Forst, and Camptostemon philippinense (S.Vidal) Becc which were also considered as native species to the Philippines. In IUCN red list (IUCN, 2021-2), three species were found to be threatened, and categorized as Endangered (Camptostemon philippinense (S.Vidal) Becc), Vulnerable (Avicennia rumphiana Hallier f.), and Near Threatened (Aegiceras floridum Roem. & Schult). Pemphis acidula J.R.Forst. & G.Forst species was categorized as Endangered by DENR (DAO, 2017-11), but in IUCN (IUCN, 2021-2) the species was still in Least Concern category (Table 3). Then Avicennia rumphiana Hallier f. and Aegiceras floridum Roem species were categorized as threatened in IUCN (IUCN, 2021-2), but in DENR (DAO, 2017-11) the species were now categorized as not yet assessed. As observed in the sampling sites, the two species were still dominant in the wild.

Villanueva and Buot (2015) reiterating that in updating the conservation status of an individual species are actually based on the area and species priority of an accrediting institution. Accrediting institution with larger area of coverage could hardly update its record regularly, as compared to a local accrediting institution.

Conservation status of Mangrove species in Camotes Island using DENR-DAO and IUCN category
Species Family name Conservation Status
Scientific name Common name DAO 2017-11 IUCN 2021-2
Acanthus ebracteatus Vahl Lagiwliw Acanthaceae Not yet assessed Least concern
Acanthus volubilis Wall Lagiwliw Acanthaceae Not yet assessed Least concern
Aegiceras corniculatum (L.) Blanco Saging2x Primulaceae Not yet assessed Least concern
Aegiceras floridum Roem. & Schult Saging2x pula Primulaceae Not yet assessed Near Threatened
Avicennia alba Blume Api-api Acanthaceae Not yet assessed Least concern
Avicennia marina (Forssk.) Vierh Miapi Acanthaceae Not yet assessed Least concern
Avicennia officinalis L. Bungalon Acanthaceae Not yet assessed Least concern
Avicennia rumphiana Hallier f. Bungalon Acanthaceae Not yet assessed Vulnerable
Bruguiera cylindrica (L.) Blume Pototan Rhizophoraceae Not yet assessed Least concern
Bruguiera gymnorhiza (L.) Savigny in Lam Busain Rhizophoraceae Not yet assessed Least concern
Bruguiera parviflora (Roxb.) Wight & Arn. ex Griff Langarai Rhizophoraceae Not yet assessed Least concern
Bruguiera sexangula (Lour.) Poir Malatalong Rhizophoraceae Not yet assessed Least concern
Camptostemon philippinense (S.Vidal) Becc Gapas2x Bombacaceae Endangered Endangered
Ceriops tagal (Perr.) C.B.Rob Tungog Rhizophoraceae Not yet assessed Least concern
Ceriops zippeliana Blume Lapis2x Rhizophoraceae Not yet assessed Least concern
Excoecaria agallocha L., Syst Buta2x Euphorbiaceae Not yet assessed Least concern
Lumnitzera littorea (Jack) Voigt Tabao pula Combretaceae Not yet assessed Least concern
Lumnitzera racemosa Willd Culase Combretaceae Not yet assessed Least concern
Nypa fruticans Wurmb Nipa Arecaceae Not yet assessed Least concern
Osbornia octodonta F. Muell. Tawalis Myrtaceae Not yet assessed Least concern
Pemphis acidula J.R.Forst. & G.Forst Bantigi Lythraceae Endangered Least concern
Rhizophora apiculata Blume Bakhaw lalaki Rhizophoraceae Not yet assessed Least concern
Rhizophora lamarckii Montrouz Bakhaw hybrid Rhizophoraceae Not yet assessed Not evaluate
Rhizophora mucronata Poir. Bakhaw babae Rhizophoraceae Not yet assessed Least concern
Rhizophora stylosa Griff. Bakhaw bato Rhizophoraceae Not yet assessed Least concern
Scyphiphora hydrophylacea C.F.Gaertn Nilad Rubiaceae Not yet assessed Least concern
Sonneratia alba Sm. Pagatpat Lythraceae Not yet assessed Least concern
Xylocarpus granatum Koen Tabigi Meliaceae Not yet assessed Least concern
Xylocarpus moluccensis (Lam.) M.Roem Lagutlot Meliaceae Not yet assessed Least concern
Acrostichum speciosum Willd Palaypay Pteridaceae Not yet assessed Least concern

Conclusion

Conservation effort and Information Education Campaign (IEC) are needed by the Local Government Units to protect the high mangrove species diversity of Camotes Island.  The Local Government Unit concerned must strictly implement the policy of protecting the mangrove species, since the whole Camotes Island was declared as protected area under Proclamation No. 2152, s. 1981. Empowerment of the local communities by legitimizing their resource use rights, as well as management responsibilities is the key factor in driving successful mangrove restoration (Camacho et al., 2020).

Acknowledgements

The authors would like to acknowledge the Department of Science and Technology (DOST) for considering and approving their research proposal.  The Philippine Consortium for Agriculture and Resource Research Development (PCAARRD) for recommending their proposal to DOST and guiding them in the implementation of the study. The CTU System and CTU Camotes Campus for supporting the research team, and allowing the research staff to conduct the study in Camotes Island. The DENR Region 7 for giving them the Gratuitous permit (GP). The Municipalities of San Francisco, Poro, Pilar, and Tudela for allowing them to conduct the study in their area of responsibilities. The first author (EPL) would like to thanks his wife (Mary Jane) and son (CJ) for their moral support, during the conduct of the study.

References