Journal of Threatened Taxa |
www.threatenedtaxa.org | 26 April 2021 | 13(5): 18247–18256
ISSN 0974-7907 (Online) | ISSN 0974-7893
(Print)
https://doi.org/10.11609/jott.6278.13.5.18247-18256
#6278 | Received 07 June 2020 | Final
received 20 July 2020 | Finally accepted 13 March 2021
Diversity of understory flowering plants in the forest patches of Marilog District, Philippines
Florfe M. Acma 1, Noe P. Mendez 2, Noel E. Lagunday 3 & Victor B. Amoroso 4
1–4 Center for Biodiversity Research and
Extension in Mindanao (CEBREM), Central Mindanao University, University Town, Musuan, 8710 Bukidnon, Philippines.
1,4 Department of
Biology, College of Arts and Sciences, Central Mindanao University, University
Town, Musuan, 8710 Bukidnon, Philippines.
1 flmacma@gmail.com
(corresponding author), 2 npolomendez@gmail.com, 3 lagundaynoel@gmail.com,
4 victorbamoroso@gmail.com
Editor: Anonymity requested. Date of publication: 26 April 2021
(online & print)
Citation: Acma,
F.M., N.P. Mendez, N.E. Lagunday & V.B. Amoroso (2021). Diversity of
understory flowering plants in the forest patches of Marilog
District, Philippines. Journal of Threatened Taxa 13(5): 18247–18256. https://doi.org/10.11609/jott.6278.13.5.18247-18256
Copyright: © Acma et al. 2021. Creative Commons Attribution
4.0 International License. JoTT allows unrestricted use, reproduction, and
distribution of this article in any medium by providing adequate credit to the
author(s) and the source of publication.
Funding: Commission on Higher Education
(CHED); Central Mindanao University (CMU).
Competing interests: The authors
declare no competing interests.
Author details: Florfe M. Acma
is a Professor of the Department of Biology, College of Arts and Sciences, and
currently the Director of the Center for Biodiversity Research and Extension in
Mindanao , Central Mindanao University, Philippines. She earned her Ph D Botany
from the University of the Philippines Los Banos and
is conducting researches on floristic studies, biodiversity and conservation
studies and on Philippine Zingiberaceae. Noe P.
Mendez currently works as an Instructor at the Biology Department of Central
Mindanao University. He was previously the program assistant of the CHED-DARE
TO-Funded research program implemented by the Center for Biodiversity Research
and Extension in Mindanao (CEBREM). Noe is also currently studying Zingiberaceae species of the Philippines. Noel E. Lagunday is working on the systematics of carnivorous
pitcher plants of Mindanao Island as his dissertation. He is also working at
the Center for Biodiversity Research and Extension in Mindanao (CEBREM),
Central Mindanao University as project assistant IV capacity for the DOST
funded research project. Victor B. Amoroso is a Professor Emeritus of Central
Mindanao University and is also an Academician of the National Academy of
Science and Technology (NAST) of the Philippines. Dr. Amoroso is a famous pteridologist and has worked on other groups of plants like
Nepenthaceae and other families of plants. He has
played significant role in the establishment of the Center for Biodiversity
Research and Extension in Mindanao and has led many biodiversity researches
which encompass mountain ecosystems of
Mindanao. His research interest is on biodiversity, conservation and
development of food products and biopesticides from indigenous plants.
Author contribution: VBA has conceptualized and proposed the research and
is the program leader of the research. FMA is the Research Project Leader who
helped the Program Leader in the implementation of the research. FMA, NPM, NEL and VBA collected, processed
and identified specimens and likewise analyzed the data. FMA and NPM drafted
the manuscript while VBA and NEL improved the manuscript.
Acknowledgements: We thank the
Commission on Higher Education (CHED) for funding this study under the
Discovery-Applied Research and Extension for Trans/Inter-disciplinary
Opportunities (DARE-TO) Program. The
Department of Environment and Natural Resources (DENR) for the issuance of
gratuitous permit; Matigsalug-Manobo Tribal People
Council of Elders Davao, Inc. (MAMATRIPCEDI) and Local Government Units (LGUs)
of Brgy. Baganihan, Brgy. Datu Salumay,
and Marahan Proper for allowing and supporting the
researchers to conduct this study; and to our local researchers for
accompanying us during the botanical fieldworks.
Abstract: The forest patches of
Marilog District, Davao are the remnants of various
anthropogenic activities including logging, conversion of land for agriculture,
ecotourism and human settlements. Floristic
study was carried out in 2018–2019 from 100 established plots measuring 20 x 20
m, with repeated transect walks and opportunistic sampling along forest
trails. One-hundred-and-four species of
understory flowering plants were identified from 102 genera and 40 families. Species diversity mean values across study
sites using Simpson’s (D) and Shannon-Wiener index (H’) were 0.97
and 3.9, respectively. Species diversity
was highest in sites 2 and 4 (D = 0.98; H’ = 4.0 each) and lowest
in site 5 (D = 0.96; H’ = 3.7).
At family level, the most abundant taxa include Zingiberaceae
(26 species) (15%), Orchidaceae (19 species) (11%), Gesneriaceae (14 species) (8%), and Rubiaceae
and Arecaceae (13 species each) (7%). Conservation status assessment using
International Union for Conservation of Nature (IUCN) revealed 10 threatened
species, while listing from the Philippines’ administrative order has
categorized 13 threatened species. A
total of 54 species (ca. 1.14% of the total Philippine endemic vascular flora)
of understory flowering plants were Philippine endemics. Findings of this study were used as
additional data for the proclamation of Mt. Malambo
as Local Conservation Area, which was formalized through a barangay resolution.
Keywords: Epiphytes, herbs,
lianas, southern Philippines, threatened species, vines.
INTRODUCTION
The Philippine
vascular flora has at least 10,158 species which are distributed to 1,942
genera in 279 families. Of these, 9,038
species are angiosperms (Pelser et al. 2011 onwards),
which include understory plants.
Understory species contribute to erosion control and nutrient capture
(Gilliam 2007). The understory plant
communities are considered good ecological indicators of forest health
(Tremblay & Larocque 2001; Kerns & Ohmann 2004), biodiversity, habitat potential, umbrella
species sustainability, global change impact, and disturbance risk assessment (Suchar & Crookston 2010).
Tropical montane
forests are important for the provision of ecosystem services (Martínez et al.,
2009). The forest patches of Marilog District, Davao City, Philippines can be classified
as tropical lower montane rainforests owing to its elevation and as “Baguio de
Mindanao” due to its relatively cool temperature. Twenty-five years ago, Amoroso et al. (1996)
reported that Marilog forest has a clay loam soil
type with elevations ranging 1,150–1,290 m.
It is also home to numerous vascular flora with at least two plant
species recently recorded in this country for the first time (see Amoroso et
al. 2018a; Acma et al. 2019); however, humans are
altering the composition of biological communities through a variety of
activities, which endanger some of the plant species in the area. Some of these anthropogenic activities
include plant trading and over-collection from the wild, and conversion of the
forests into rest houses, restaurants, mountain resorts and farmlands. Hence, these scenarios prompted the authors
to conduct an inventory and assessment of understory plants in the forest
patches of Marilog District, specifically the
understory flowering plants which were not yet documented.
METHODS
Permit Statement
This study was
conducted from February 2018 to September 2019 after necessary permits were
obtained from respective agencies, such as Barangay resolutions from Brgy. Baganihan, Brgy. Datu Salumay,
and Marahan Proper; prior informed consents (PIC’s);
memorandum of agreement (MOA) between Central Mindanao University and the Matigsalug-Manobo Tribal People Council of Elders Davao,
Inc. (MAMATRIPCEDI); and wildlife gratuitous permit from the Department of
Environment and Natural Resources (DENR) - Region XI.
Study area and study
sites
Floristic inventory
was conducted in the five forest patches of Marilog
District, which are geopolitically part of Brgy. Baganihan and Brgy. Datu Salumay situated in the
northern part and Marahan Proper in the south (Fig.
1). The established sites were found
within the forest patches of Marilog District and the
sites are: Purok-5, Sitio New Calinan and Sitio Maharlika, Brgy. Baganihan (site 1); Mt. Malambo, Brgy. Datu Salumay
(site 2); Lola Mommy’s Rainforest, Sitio Epol, Brgy. Baganihan (site 3); Mt. Ulahingan, Sitio Tagumpay, Brgy. Datu Salumay
(site 4); and Sitio Matigsalug, Marahan
Proper (site 5).
Sites 1–4 are
tropical lower montane rainforests, while site 5 is mixed to agro forest ecosystems with elevations ranging 1,000–1,345
m. Among the sites, site 2 had the
highest elevation range (1,197–1,345 m).
Soil substrates are clay & limestone (sites 1, 3 & 4) and clay
& loam (sites 2 & 5) (Table 1).
The explored forest patches in these sites were dominated by Lithocarpus spp. (Fagaceae),
Canarium spp. (Burseraceae),
Palaquium philippense
(Perr.) C.B. Rob. (Sapotaceae),
Ficus spp. (Moraceae),
Syzygium spp. (Myrtaceae),
Astronia ferruginea
Elmer (Melastomataceae), and Cinnamomum
spp. (Lauraceae).
Establishment of
Sampling Plots and Field Sampling
Establishment of the
sampling sites was based on Google Earth maps and in consultation with the
barangay officials, council of elders, and tribal leaders. The presence of forests or forest patches was
the primary consideration in the selection of the sites to capture the
naturally growing plants in the area.
The understory flowering plants were inventoried and assessed through
repeated transect walks, opportunistic sampling, and documentation from the 100
established 20 x 20 m quadrats in the five sampling sites.
Collection and
Processing of Specimens
The collection of
plants was done by uprooting the whole plant or by cutting branches preferably
with reproductive parts. The specimens
were pressed in newspapers, labeled with collection
number, collectors, field identification (with local names if available), site
of collection, coordinates and elevations. Cardboards were placed in between
sheets and tied using a twine. The
herbarium specimens were then placed inside the transparent cellophane bags,
processed following the wet method, and dried using a mechanical dryer. The dried herbarium specimens were deposited
at the Central Mindanao University Herbarium (CMUH) for accessioning. Herbarium specimens were limited to three
individuals of plant or plant parts per species per site as stipulated in the
wildlife gratuitous permit.
Identification of
Specimens and Assessment
Field guides, online
database (e.g., JSTOR, Co’s Digital Flora of the Philippines of Pelser et al. 2011 onwards), and literature (Aribal 2013; Amoroso et al. 2018b) were used to identify
the voucher specimens.
Conservation status
of the species were determined based on Department of Environment and Natural
Resources (DENR) Administrative Order (DAO 2017–11), International Union for
Conservation of Nomenclature (IUCN) (IUCN 2020) and publications. The ecological status of plants were assessed
using Co’s Digital Flora of the Philippines (Pelser
et al. 2011 onwards) and DAO (2017–11).
Data Treatment and
Analysis
The biodiversity
index values were calculated using Simpson (1948), Shannon and Wiener (1963),
and Magurran (2004).
The Shannon-Wiener index (H’) was applied as measure of both
species abundance and richness to quantify diversity of the understory
flowering plants, while Simpson’s index of diversity gives the probability that
any two individuals drawn at random from infinitely large community belonging
to the same species. Calculation for
frequency, relative frequency, density, relative density and Importance Value
Index (IVI) were derived from (Nguyen et al. 2015). The following formulae were used:
s
Shannon-Wiener index
(H') = -Σ Pi ln Pi
i=1
where pi = ni/N, where ni is the number of
individuals in species i and N is the total number of
individuals in the community and ln is the natural logarithm.
s ni (ni-1)
Simpson’s index = -Σ ––––––––– i=1 N(N-1)
where ni is the number of individuals in species i and N is the total number of individuals in the
community.
H’ Σ Pi ln Pi
Species eveness =
––––––––– = –––––––––
H’max
ln s
where s = number of
species; pi = proportion of individuals or abundance of the ith
species expressed as a proportion
of total cover.
Number
of a species
Density = –––––––––––––––––––
Total area sampled
Area of plots in which species occurs
Frequency =
––––––––––––––––––––––––––––––––
Total area sampled
Density of a species
Relative density (RD)
=––––––––––––––––––––x 100
Total density of all species
Frequency of a species
Relative frequency
(RF) =––––––––––––––––––x 100
Total frequency of
all species
and Species
importance value index (IVI) = RD + RF.
RESULTS AND DISCUSSION
Species richness and
composition across study sites
The study documented
a total of 174 species of understory flowering plants, which belong to 102
genera and 40 families. Site 1 had the
highest number of species (109 species), followed by site 4 (92 species), site
2 (89 species), site 3 (88 species), and site 5 (83 species) (Fig. 2). These understory flowering plants include
herbs, vines, lianas, epiphytes, palms, and rattans. The relatively high species richness in site
1 can be attributed to the environmental and ecological conditions, ample
sunlight and a variety of microhabitats present in the area where the
understory flowering plants can favorably grow. The species which dominated in site 1 is Freycinetia sp. 2 (Pandanaceae)
(10%), Pandanus sp. (Pandanaceae) (6%) in site
2 (6%), Curculigo sp. (Hypoxidaceae) (9%) in site 3, Dendrochilum
sp. (Orchidaceae) (4%) in site 4, and Pandanus
sp. 2 (12%) in site 5 (Table 2).
The total understory
plants documented in this study is relatively high compared to the studies
conducted at the expansion sites of Mt. Hamiguitan
Range Wildlife Sanctuary (MHRWS) by Amoroso et al. (2018b) with 30 species
(referred as herbs and vines) and Amoroso et al. (2018c) with 29 species
(termed as other plants). Since the
study area is a tropical lower montane rainforest, current findings support the
report of Kessler et al. (2010) that several factors may affect local montane
species richness in the Philippines, such as the size of the area sampled,
climate conditions, soil type, and geographic location.
Furthermore, it is
noteworthy that the species richness reported herein is relatively high
compared to the previous studies (Alava 2001; Agduma
et al. 2011; Aribal 2013) which included the trees,
shrubs, ferns, and lycophytes in their reports.
The current study reported only the flowering understory plants
excluding the trees, shrubs, pteridophytes and lycophytes, but has higher
number of species compared to Alava (2001) who recorded 161 species in Mt. Mayapay; Agduma et al. (2011)
with 101 species in Plantinum Rubber Plantation, Makilala, North Cotabato; and Aribal (2013) with 92 species in Caimpugan
Peat Swamp Forest.
At family level, the
most abundant taxa include Zingiberaceae (26 species)
(15%), Orchidaceae (19 species) (11%), Gesneriaceae (14 species) (8%), and Arecaceae
and Rubiaceae (13 species) (7%) (Fig. 2). The
significant number of Zingiberaceae in the area,
especially in Brgy.
Baganihan (sites 1 and 3) can be attributed to
the presence of water bodies, environmental, and ecological conditions. The number of Zingiberaceae
species collected is the highest number in a certain geographical area in the
country as of to date (Acma et al. submitted).
In Mt. Malambo (site 2), two species of understory plants were
recently reported as new family record and new species record, viz., Mitrastemon yamamotoi
Makino (Mitrastemonaceae) (Amoroso et al. 2018) and Plagiostachys albiflora
Ridl. (Zingiberaceae) (Acma et al. 2019), respectively.
Rasingam & Parthasarathy
(2009), recorded a total density of understory plants of 851 ha-1 (6,812 individuals) and a species
richness of 108 species (104 genera and 50 families) in forests of Little
Andaman Island, India. In comparison,
the present study recorded a greater species richness (174 species); however, the study of Xiao-Tau et al. (2011)
reported the presence of 3068 individuals of understory plants belonging to 309
species in 192 genera and 89 families in the tropical seasonal forests of Xishuangbanna, southern China in a 100m2 area.
Further, Swamy et al. (2000)
reported a total of 244 species (183 genera and 76 families) in their study on
the vegetation structure and species composition of tropical ecosystems in
reserve forests in the Western Ghats of Tamil Nadu, India. It was also noted that greater diversity was
recorded in mid-elevation forests.
Species Diversity
Species diversity
values (mean) across study sites using Simpson’s (D) and Shannon-Wiener
index (H’) are 0.97 and 3.9, respectively.
Species diversity is highest in site 2 (D = 0.98; H’ =
4.0) and site 4 (D = 0.98; H’ = 4.0), followed by sites 3 (D
= 97; H’ = 3.9), site 1 (D = 0.96; H’ = 3.8) and lowest in
site 5 (D = 0.96; H’ = 3.7) (Fig. 3). Shannon-Wiener diversity values in the study
sites are greater than typical values (1.5 – 3.5) in most ecological studies (Maguran, 1988; Maguran
2004). The results suggest that site 2
(Mt. Malambo) and site 4 (Mt. Ulahingan)
are equally the most diverse in understory flowering plants. The low diversity value in Site 5 (Sitio Matigsalug) is attributed to its secondary grown and
fragmented forest with dry substrates making the forest not suitable for plants
to survive.
Species evenness is
highest in site 4 (0.89), followed by site 2 (0.88), site 3 (0.86), site 5
(0.83) and was lowest in site 1 (0.80) (Fig. 3). The species evenness implies how equal the
community is numerically.
Species Importance
Value Index (IVI)
The inventory of
flowering understory plants revealed that Freycinetia
sp. 2 (IVI =13.3) obtained the highest importance value index (IVI) in site 1, Pandanus
sp. (IVI = 11) in site 2, Curculigo sp.
(IVI = 13) in site 3, Rubus sp. (IVI =
7) in site 4, and Pandanus sp. 2 (IVI = 16.4) in site 5 (Table
3).
Marilog District is home to
five species of Tetrastigma, with Tetrastigma sp. 1 as the most observed in all
sampling sites; however, identification up to the species level was not
possible, since flowering and fruiting materials of the species were not
available at the time of sampling. Calamus
mollis Blanco, C. filispadix
Becc., Pandanus sp. 1, and Pandanus sp.
2 were the most common rattans and pandans in the
area. This implies that these species
play important roles in the ecosystem and elimination of these species would
result to changes in plant community structure.
Conservation Status
and Endemism
Conservation status
assessment revealed one Critically Endangered (CR), one Endangered (EN), seven
Least Concern (LC), and two Data Deficient (DD) species following the IUCN
(2020). The DAO (2017–11) listed three
EN species, two Vulnerable (VU), and eight other threatened species (OTS). Mitrastemon
yamamotoi Makino proposed as CR by Amoroso et al.
(2018) was only observed in site 2 (Table 4; Image 1). Among these species, Monophyllaea
merilliana Kraenzl.
(OTS) was observed in sites 1–4 in limestone karst habitat. On the other hand, a total of 54 species of
understory flowering plants were Philippine endemics. This number constitutes ca. 1.14% of
the total Philippine endemic vascular flora.
Threats observed in
the sampling sites
Ongoing habitat
degradation through land conversion for agriculture and human settlements, and
rampant small-scale harvesting of wild plants from the forests, are documented
biodiversity threats in Marilog District. If these activities are not mitigated, the
number of species will likely decline and economically-important species will
be depleted in the areas.
CONCLUSIONS AND RECOMMENDATIONS
This study concludes
that the Marilog District forests harbor
a rich understory plant community (174 species) which is distributed in 102
genera and 40 families. The sites having
high elevation and with intact forest had the highest diversity: Site 2, Mt . Malambo and site 4, Mt. Ulahingan
(D = 0.98; H’ = 4.0). Each
site is unique as evidenced by the species which obtained the highest
importance value index of the site. Freycinetia sp. 2 (IVI = 13.3) for site 1, Pandanus
sp. (IVI = 11) for site 2, Curculigo sp.
(IVI = 13) for site 3, Rubus sp. (IVI =
7) for site 4, and Pandanus sp. 2 (IVI = 16.4) for site 5. Conservation efforts should be done since the
13 threatened species recorded and 54 species overall are Philippine endemics,
which represent ca. 1.14% of the total Philippine endemic vascular
flora.
It is therefore
imperative that the results gathered from this study be cascaded to the local
government units (LGU’s) and stakeholders to create more awareness of the
richness of the understory flora in their locality and formulate additional
policies and strategies for the protection and conservation of these important
biological resources. Ex situ and in
situ conservation are also recommended to properly protect and conserve the
species and their habitats.
Table 1. Elevation,
soil substrates and number of established plots in the study sites.
Study site |
Elevation (masl) |
Soil substrate |
No. of plots (20x20 m) |
Site 1 (Sitio New Calinan and Maharlika) |
1220–1240 |
clay & limestone |
20 |
Site 2 (Mt. Malambo) |
1197–1345 |
clay & loam |
20 |
Site 3 (Sitio Epol) |
1151–1178 |
clay &
limestone |
20 |
Site 4 (Mt. Ulahingan) |
1280–1320 |
clay &
limestone |
20 |
Site 5 (Sitio Matigsalug) |
1,000–1,200 |
clay & loam |
20 |
Table 2. Dominant
species across the study sites.
Study site |
No. of species |
No. of individuals |
Dominant species |
Dominance (%) |
Site 1 |
109 |
2523 |
Freycinetia sp. 2 |
10 |
Site 2 |
89 |
903 |
Pandanus sp. |
6 |
Site 3 |
88 |
1217 |
Curculigo sp. |
9 |
Site 4 |
92 |
1184 |
Dendrochilum sp. |
4 |
Site 5 |
83 |
947 |
Pandanus sp. 2 |
12 |
Table 3. Top three
species of understory flowering plants with high Importance Value Index (IVI).
Study site |
Species |
IVI |
Site 1 |
Freycinetia sp. 2 |
13.3 |
|
Tetrastigma sp. 1 |
12.3 |
|
Calamus mollis Blanco |
11 |
Site 2 |
Pandanus sp. 1 |
11 |
|
Tetrastigma sp. 1 |
7.4 |
|
Musa textilis Nées |
7.1 |
Site 3 |
Curculigo sp. |
13 |
|
Sarcandra glabra (Thunb.) Nakai |
9 |
|
Mackinlaya celebica (Harms) Philipson |
8 |
Site 4 |
Rubus sp. |
7 |
|
Plagiostachys escritorii Elmer |
7 |
|
Pandanus sp. 1 |
6.2 |
Site 5 |
Pandanus sp. 2 |
16.4 |
|
Calamus mollis Blanco |
14 |
|
Calamus filispadix Becc. |
11 |
Table 4. Conservation
status of understory flowering plants in Marilog
Forest Reserve.
Family |
Taxon |
Conservation
status |
||
|
|
IUCN (2020) |
DENR (2017) |
Endemicity Pelser et al. (2011
onwards) |
Apocynaceae |
Hoya apoensis Kloppenb.
& Siar. |
|
|
PE |
Araceae |
Alocasia heterophylla (C.Presl) Merr. |
|
|
PE |
|
Alocasia sanderiana W.Bull |
CR |
EN |
PE |
Araliaceae |
Schefflera simplicifolia Merr. |
|
|
PE |
Arecaceae |
Calamus bicolor Becc. |
|
|
PE |
|
C. cumingianus Becc. |
|
|
PE |
|
C. filispadix Becc. |
|
|
PE |
|
C. microcarpus Becc. |
|
|
PE |
|
C. mollis Blanco |
|
OTS |
PE |
|
C. spinifolius C.Mart. |
|
|
PE |
|
Heterospathe philippinensis (Becc.) Becc. |
|
|
PE |
|
Pinanga copelandii Becc. |
|
|
PE |
|
P. philippinensis Becc. |
|
|
PE |
|
P. speciosa Becc. |
|
|
PE |
|
P. woodiana Becc. |
|
|
PE |
Begoniaceae |
Begonia mindanaensis Warb. |
|
|
PE |
|
B. pseudolateralis Warb. |
LC |
|
|
Fabaceae |
Strongylodon pulcher C.B.Rob. |
|
|
PE |
Gesneriaceae |
Aeschynanthus asclepioides (Elmer) B.L.Burtt & P.Woods |
|
|
PE |
|
A. cardinalis (Copel. ex Merr.) Schltr. |
|
|
PE |
|
Agalmyla chorisepala (C.B.Clarke)
Hilliard & Burtt |
|
|
PE |
|
A. clarkei (Elmer) B.L.Burtt |
|
|
PE |
|
A. persimilis Hilliard & B.L.Burtt |
|
VU |
PE |
|
Cyrtandra tagaleurium Kraenzl. |
|
|
PE |
|
Monophyllaea merilliana Kraenzl. |
|
OTS |
|
Melastomataceae |
Medinilla clementis Merr. |
|
OTS |
PE |
|
M. copelandii Merr. |
|
|
PE |
Mitrastemonaceae |
Mitrastemon yamamotoi Makino |
|
CR |
|
Nepenthaceae |
Nepenthes mindanaoensis Sh.Kurata |
LC |
VU |
PE |
|
N. truncata Macfarl. |
EN |
EN |
PE |
Orchidaceae |
Ceratostylis retisquama Rchb.f. |
|
|
PE |
|
Coelogyne candoonensis Ames |
|
|
PE |
|
C. cloroptera Rchb.f. |
|
|
PE |
|
Phaius philippinensis N.E.Br. |
|
|
PE |
|
Trichotosia odorifera (Leav.)
Kraenzl |
|
|
PE |
Pandanaceae |
Freycinetia jagorii Warb. |
|
|
PE |
|
F. negrosensis Merr. |
|
|
PE |
|
F. sphaerocephala Gaudich. |
|
|
PE |
Piperaceae |
Piper ensifolium Quisumb. |
|
|
PE |
Rubiaceae |
Oldenlandia apoensis Elmer |
|
|
PE |
|
Psychotria cuernosensis Elmer |
|
|
PE |
Urticaceae |
Procris brunnea Merr. |
|
|
PE |
|
P. urdanetensis Elmer |
|
|
PE |
Zingiberaceae |
Adelmeria alpina Elmer |
LC |
|
PE |
|
Alpinia haenkei C.Presl |
LC |
|
PE |
|
A. rufa C.Presl |
|
|
PE |
|
Amomum dealbatum Roxb. |
DD |
|
|
|
Etlingera elatior (Jack.) R.M.Sm. |
DD |
|
|
|
E. fimbriobracteata (K.Schum.) R.M.Sm. |
DD |
|
|
|
E. philippinensis (Ridl.) R.M.Sm. |
|
|
PE |
|
E. pubimarginata (Elmer) A.D.Poulsen |
|
|
PE |
|
Globba campsophylla K.Schum. |
LC |
|
PE |
|
Hedychium philippinense K.Schum. |
|
EN |
PE |
|
Hornstedtia conoidea Ridl. |
|
|
PE |
|
H. lophophora Ridl. |
|
|
PE |
|
Meistera muricarpa (Elmer) Škorničk.
& M.F.Newman |
|
|
PE |
|
Plagiostachys albiflora Ridl. |
LC |
|
|
|
P. escritorii Elmer |
|
|
PE |
|
Wurfbainia hedyosma (I.M.Turner)
Škorničk. & A.D.Poulsen |
|
|
PE |
|
W. mindanaensis (Elmer) Škorničk. & A.D.Poulsen |
|
|
PE |
|
Zingiber banahaoense Mood & Theilade |
|
|
PE |
Legends:
CR-—Critically Endangered | EN—Endangered | VU—Vulnerable | OTS—Other
Threatened Species | LC—Least Concern | DD—Data Deficient | PE—Philippine
endemic
For
figures & images - - click here
REFERENCES
Acma, F.M., N.P. Mendez,
N.E. Lagunday & V.B. Amoroso (2019). New record of Plagiostachys albiflora
Ridl. (Zingiberaceae) in
the Philippines. Modern Phytomorphology 13:
5–8. https://doi.org/10.5281/zenodo.190102
Agduma, A.R., M.J.M.M. Achondo, B.L.P. Bretana, V.P.
Bello, L.L. Remollo, L.S. Mancao,
J.P. Supremo, J.G.C. Salem & F.R.P. Salvana
(2011). Diversity of vascular plant species in an agroforest:
the case of a rubber (Hevea brasiliensis) plantation in Makilala,
North Cotabato. Philippine Journal of Crop Science
36(3): 57–64.
Alava C. (2001). Ecosystematics
Studies of Trees and Pteridophytes in Two Forests in Mindanao. PhD
Dissertation. Department of Biology, Central Mindanao University, Musuan, Bukidnon, Philippines.
Amoroso, V.B., F. Acma &
H. Pava. (1996). Diversity, status and
ecology of Pteridophytes in three forests in Mindanao. Pteridology in
Perspective. Royal Botanic Gardens, Kew, London, UK. 55-60.
Amoroso, V.B., N.P. Mendez & N.E. Lagunday (2018a). Mitrastemonaceae:
A New Family Record for the Philippines. Philippine Journal of Science
147(4): 775–779.
Amoroso, V.B., F.M. Acma,
F.P. Coritico, F.S. Gorme,
N.E. Lagunday, M.C.S. Salolog
& R.D. Colong (2018b). Floral diversity
assessment of the buffer zones and vicinity of the Mt. Hamiguitan
Range Wildlife Sanctuary (MHRWS), Davao Oriental: basis for inclusion to
protected area zone. Philippine Journal of Systematic Biology 12(2):
36–51.
Amoroso, V.B., A.B. Mohagan,
F.P. Coritico, A.G. Ponce, D.O. Amper,
S.S. Zamora, F.S. Gorme, R.D. Colong
& R.G. Ponce (2018c). Biodiversity Assessment in the Buffer Zone of
Mt. Hamiguitan Range Wildlife Sanctuary. CHED
Terminal Report.
Aribal, L.G. (2013). Plant Diversity and
Structure of the Caimpugan Peat Swamp Forest on Mindanao
Island, Philippines. PhD Dissertation. Department of Forest Biological
Sciences. University of the Philippines, Los Baños,
College, Laguna.
Gilliam, F.S. (2007). The ecological
significance of the herbaceous layer in temperate forest ecosystems. Bioscience
57: 845–858.
IUCN (2020). The IUCN Red List of
Threatened Species. Accessed at: https://www.iucnredlist.org/. Accessed on 30
April 2020.
Kerns, B.K. & J.L. Ohmann
(2004). Evaluation and prediction of shrub cover in coastal
Oregon forests (USA). Ecological Indicators 4: 83–98.
Kessler, M., J. Kluge, A. Hemp & R. Ohlemüller (2011). A global comparative
analysis of elevational species richness patterns of ferns. Global Ecology
and Biogeography 20: 868–880.
Martínez, M.L., O. Pérez-Maqueo,
G. Vázquez, G. Castillo-Campos, J. García-Franco, K. Mehltreter,
M. Equihua & R. Landgrave (2009). Effects of land use
change on biodiversity and ecosystem services in tropical montane cloud forests
of Mexico. Forest Ecology Management 258: 1856–1863.
Magurran, A.E. (1988). Ecological
Diversity and its Measurement. Princeton University Press, Princeton, NJ.
Magurran, A.E. (2004). Measuring
Biological Diversity. Blackwell.
Nguyen, H., D. Lamb, J. Herbohn
& J. Firn (2015). Equations to
calculate Important value index (IVI) of species. PLOS ONE. Dataset.
https://doi.org/10.1371/journal.pone.0095267.t00
Pelser, P.B., J.F.
Barcelona, D.L. Nickrent (eds.) (2011 onwards). Co’s Digital Flora
of the Philippines. Accessed from: www.philippineplants.org. Accessed on 03
April 2020.
Rasingam, L. & N.
Parthasarathy (2009). Diversity of understory plants in undisturbed and
disturbed tropical lowland forests of Little Andaman Island, India. Biodiversity
and Conservation 18: 1045–1065.
Shannon, C.E. & W. Wiener (1963). The Mathematical
Theory of Communication. University of Illinois Press, Urbana, 117pp.
Suchar, V.A. & N.L.
Crookston (2010). Understory cover and biomass indices predictions
for forest ecosystems of the Northwestern United
States. Ecological Indicators 10: 602–609.
Swamy, P.S.,
S.M. Sundarapandian, P. Chandrasekar & S.
Chandrasekaran (2000). Plant species diversity and tree population
structure of a humid tropical forest in Tamil Nadu, India. Biodiversity and Conservation 9:
1643–1669.
Tremblay, N.O. & G.R. Larocque
(2001). Seasonal dynamics of understory Vegetation in four
eastern Canadian forest types. International Journal of Plant Sciences
162: 271–286.
Xiao-Tau L., Y. Jiang-Xia & T. Jian-Wei (2011). Diversity and
Composition of Understory Vegetation in the tropical seasonal rainforest of Xishuangbanna, SW China. Revista
de Biología Tropical 59(1): 455–463.