Richness and Distribution of Orchids (Orchidaceae) in The Forests of Mount Busa, Sarangani, Southern Mindanao, Philippines

You might also like

Download as pdf or txt
Download as pdf or txt
You are on page 1of 13

Philippine Journal of Science

150 (S1): 151-163, Special Issue on Biodiversity


ISSN 0031 - 7683
Date Received: 21 Sep 2020

Richness and Distribution of Orchids (Orchidaceae)


in the Forests of Mount Busa, Sarangani,
Southern Mindanao, Philippines

Aljohn Jay L. Saavedra1,2 and Kier Mitchel E. Pitogo2

1PhilippineTaxonomic Initiative, Inc.


El Nido, Palawan 5313 Philippines
2Departmentof Environment and Natural Resources
Provincial Environment and Natural Resources Office South Cotabato
Block 1, Martinez Subdivision, Koronadal City 9506 Philippines

Orchids are one of the most diverse yet threatened plant families in the world and the Philippines.
Despite the new species discoveries of orchids in the country in recent years, diversity and
distribution studies are still severely lacking. Here, we provide a list of orchid species found
among different forest types in Mount Busa and provide information on the species’ altitudinal
and vertical distributions and ornamental use. We recorded 108 species of orchids from 51
genera, of which 53 species are endemic to the Philippines and 15 species are known only to
occur on Mindanao island. Species composition differed among forest types, with the MASLEF
(mixed advanced secondary lowland evergreen forest) hosting the highest number of orchid
species recorded, followed by the UMF (upper montane forest), LMF (lower montane forest),
and MESLEF (mixed early secondary lowland evergreen forest). Our results suggest a relatively
rich and distinct orchid diversity among different forest types in Mount Busa that reinforces
the high conservation value of the mountain range.

Keywords: Mindanao biodiversity, Oberonia serrulata, orchid conservation, orchid distribution,


orchid inventory, Philippine orchids

INTRODUCTION orchids are the most threatened group of plants globally


(Gale et al. 2018) and in the Philippines (Fernando et
Orchids are one of the largest and most diverse groups al. 2008a). It is estimated that 56.5% of the 948 orchid
among the Philippine flowering plants harboring over species assessed in the Global IUCN Red List in 2017
1200 species, varieties, and forms (Cootes 2011), with are threatened with extinction (Gale et al. 2018). In
more new species and genera being discovered and the Philippines, 97 species are already threatened that
recorded yearly (e.g. de Leon et al. 2017; Naive and represents ~ 8.1% of the orchid species recorded in the
Martyr 2018; Meneses and Cootes 2019; Naive et al. country (DENR 2017).
2019; Tamayo et al. 2020; Tandang et al. 2020). This
group of plants is mostly habitat specialists owing to Habitat destruction and unsustainable harvesting are the
their specialized reproductive strategies and mycorrhizal major global threats to orchids (Fay 2018; Gale et al. 2018).
specificity (Gravendeel et al. 2004). Unfortunately, Habitat fragmentation negatively impacts species richness
of orchids (Hundera et al. 2013; Parra Sánchez et al. 2016),
*Corresponding Authors: pitogo.kiermitchel@gmail.com

151
Philippine Journal of Science Saavedra and Pitogo: Orchids of Mt. Busa
Vol. 150 No. S1, Special Issue on Biodiversity

and their highly specialized habit makes orchids more ecology and addresses the gaps in our knowledge and
vulnerable to global environmental changes (Fay 2018). distribution of Philippine orchids. Our results would be
Orchids are also highly traded mainly for horticulture, helpful not only in elucidating the level of biodiversity in
medicine, and food (Hinsley et al. 2017). Despite being southern Mindanao but also in inferring patterns of plant
regulated under the Convention on International Trade in diversity and biogeography in the Philippines.
Endangered Species, many of the species are still being
collected and traded undocumented negatively affecting
wild populations around the world (Fay 2015).
MATERIALS AND METHODS
The increasing pressure on wild orchid populations
put orchids as a group of urgent conservation concern.
Despite the new orchid species discoveries in recent years, Study Area
diversity and distribution studies are still severely lacking We surveyed orchid species richness along the southern
(Buenavista 2017; Betanio and Buenavista 2018). This gap slope of Mount Busa, Kiamba Municipality, Sarangani
may pose conservation challenges for this highly threatened Province between July 2019 and August 2020. Mount
plant family, as assemblage-level studies may serve as Busa, known as “Bulul Tembob” among the local Tboli,
baselines for future monitoring programs in Philippine is located at N 06°06.537’ E 124°41.026’ and reaches
montane ecosystems, particularly for the highly collected 2046 m in elevation, which makes it the highest point in
and traded orchids. Distribution studies also help inform Sarangani. It houses one of the last remaining primary
species conservation assessments (e.g. IUCN Red List forests in southern Mindanao. On 10 Mar 2020, the
of Threatened Species and Philippine Red List), as these Provincial Government of Sarangani formally declared
provide information on the species’ extent of occurrence the southern slope of Mount Busa a local conservation
and geographic range. area by resolution 2020-10-042.

One of the major mountains in southern Mindanao with Mount Busa was stratified into forest types based on the
relatively intact lowland and montane forests is Mount classification of Fernando and colleagues (2008b). We
Busa. It is a key biodiversity area (KBA) and one of the further classified the lowland evergreen forest into two:
extremely high conservation priority sites in the Philippines the forest ranging in elevation from 400–600 m is the
(Ong et al. 2002). Portions of Mount Busa may have formed MESLEF and the forest from 700–1100 m elevation is the
part of the older landmass of the Zamboanga Peninsula– MASLEF. The lower elevation of Mount Busa (400–1000
Daguma Range block, which collided with the more recent m) was hardly hit during the logging concession in the
central and eastern Mindanao blocks in the Middle Miocene, early 1990s, hence the dominance of secondary-growth
thus forming the present-day Mindanao island (Sajona et trees at this elevation (see Brown 2015).
al. 1997; Hall 2002; Yumul et al. 2004). The accreted The forest from 1200–1600 m elevation is the LMF and
Mindanao island was intermittently connected directly to from 1700–2046 m elevation is the UMF (Figure 1). Five
Borneo and the rest of the Sundaland through land bridges sampling points with more than 200-m distance in between
due to repeated sea-level oscillations during the Pleistocene were randomly chosen in each forest type to maximize the
glacial cycle (Brown et al. 2013). These events may have diversity of other habitat types surveyed, although we did
shaped the present-day patterns of diversity in southern not limit our search to pre-defined plots. Habitats surveyed
Mindanao, which necessitates more field-based biodiversity include agricultural plots of abaca, riparian areas, moist
studies in Mount Busa. This is relevant for orchids, as the ravines, grasslands, shrublands, leaf litter, and forest trails.
diversity of some orchid genera in the Philippines were
shaped by this complex geological history (Guo et al. 2015;
Tsai et al. 2015, 2020). In addition, biodiversity studies in Field Sampling
southern Mindanao remain scanty, especially for orchids in Opportunistic sampling was done in each sampling site by
the region that do not have empirical field data yet available four to five experienced individuals, which entailed careful
in published literature. and extensive examinations of understory and midstory
layers of the forest for ground and epiphytic orchids. This
Here, we provide an inventory of orchid species found in was done with the caveat that orchid species beyond 4 m
Mount Busa with information on altitudinal and vertical above the ground might have not been recorded due to
distributions and their ornamental uses. Since orchid inaccessibility or observer bias. Encountered fallen trees
distribution is influenced by elevation and species’ traits and branches, however, were thoroughly searched for
(Jacquemyn et al. 2005; Zhang et al. 2015; Ding et al. 2016), canopy-dwelling orchids.
we also examined the pattern of orchid species richness
among different forest types in the area. This information The altitudinal range and vertical distribution were noted
helps improve our understanding of orchid diversity and for each orchid species observed in the wild. The altitude

152
Philippine Journal of Science Saavedra and Pitogo: Orchids of Mt. Busa
Vol. 150 No. S1, Special Issue on Biodiversity

Figure 1. A contour map of the southern slope of Mount Busa, Sarangani Province showing the sampling sites in different forest types.
MESLEF – mixed early secondary lowland evergreen forest, MASLEF – mixed advanced secondary lowland evergreen forest,
LMF – lower montane forest, UMF – upper montane forest.

was recorded using a Global Positioning System (Garmin et al. 2020), and the species’ conservation status was
64sc, USA), and the height at which the orchid was based on the DAO 2017-11 of the Philippine Department
observed (vertical distribution) was visually estimated of Environment and Natural Resources (DENR 2017).
using the height of AJS as reference. Only flowering The Philippine Department of Environment and Natural
orchid species were included in the list. We also surveyed Resources (DENR) issued the fieldwork and collection
houses in four villages, locally called as “sitios,” around permit for this study (Gratuitous Permit No. 2020-09).
the vicinity of Mount Busa (Tulad, Datal Bong, Banate,
and Green Valley) to check for orchids collected by the
Statistical Analysis
local people for ornamental use that we missed in the wild.
We examined sampling adequacy using sample-size-
All orchid species encountered were photographed in situ based and coverage-based rarefaction and extrapolation
whenever possible. We did not collect voucher specimens for (R/E) curves and a sample completeness curve for species
conservation reasons. Only one or a few individuals of most richness (data type= incidence; Chao1). These were
species of orchids recorded were observed, and many of these computed and plotted with 95% confidence intervals
species are already being collected for ornamental use. All in the R package iNEXT (Hsieh et al. 2016). A similar
species were identified based on photographic guides (Cootes analysis was used to check for orchid species richness
2001, 2011; Pelser et al. 2011 onwards), expert consultations among forest types in Mount Busa. The R/E curves allow
(e.g. through the online plant identification platform of the us to evaluate sampling completeness and facilitate a
Co’s Digital Flora of the Philippines; Barcelona et al. 2013), conservative comparison of species richness among the
and taxonomic papers in orchids (Clements and Cootes 2009; forest types despite the differences in the sampling effort.
Cabactulan et al. 2018). Only those species observed in the wild were included in
the analysis. We performed the analysis in the R statistical
We also checked the distribution of each identified species software Version 1.1.463 (R Core Team 2020).
using the aforementioned resources. Nomenclature
follows the World Checklist of Orchidaceae (Govaerts

153
Philippine Journal of Science Saavedra and Pitogo: Orchids of Mt. Busa
Vol. 150 No. S1, Special Issue on Biodiversity

RESULTS ornamental plants by the local people, 11 species were


not observed in the wild. Only five species are threatened
We recorded 108 species of orchids from 51 genera under the DAO 2017-11, one of which is listed as
(Table 1), at least four of which were putatively new critically endangered (Grammatophyllum wallisii), three
and undescribed species – namely, Bulbophyllum sp. 3, as endangered (Phalaenopsis sanderiana, Phalaenopsis
Calanthe sp., Coelogyne sp., and Dendrochilum sp. 2. reichenbachiana, Renanthera monachica), and one as
The sampling completeness curve shows that almost 50% vulnerable (Phalaenopsis mariae).
coverage was attained for all sites (Figure 2B), suggesting
that additional fieldwork would still increase the species We report range extensions of at least nine species which
richness of orchids, as shown in extrapolated curves are also new island records for Mindanao – namely,
(Figures 2A and 2C). Thrixspermum elmeri, which was previously recorded in
Negros; Cylindrolobus longissimus, Erythrodes latifolia,
The most speciose genera were Appendicula (11.1%), Rhomboda lanceolata, Blepharoglossum grossum, and
Dendrobium (9.3%), and Bulbophyllum (6.5%). Fifty- Odontochilus marivelensis in Luzon; Dendrobium boosii in
three (53) species are endemic to the Philippines, of Luzon, Mindoro, Negros, and Leyte; Agrostophyllum loheri
which 15 species are known only to occur in mainland in Cebu, Luzon, and Samar; and Paraphaius flavus in Luzon,
Mindanao. Of the 32 orchid species that were utilized as

Table 1. Initial list of orchid species in Mount Busa, Sarangani, Philippines.


Altitudinal distribution Vertical Local Endemism
No. Species Distributionc
(masl)a distribution useb
1 Acanthophippium mantinianum L.Linden & Cogn. 550 Ground Orn. Yes Philippines
2 Acriopsis liliifolia var. lilifolia (J.Koenig) Seidenf. 400–500 4m – No Widespread
3 Agrostophyllum elongatum (Ridl.) Schuit. 500 1.5–4 m – No Widespread
4 Agrostophyllum loheri Ormerod 600–700 2.5 m Orn. Yes Philippines
5 Anoectochilus sp. 800–900 Ground – – –
6 Appendicula crotalina (Ames) Schltr. 500–600 2–5 m Orn. Yes Mindanao
7 Appendicula elmeri (Ames) Ames 800 2m – Yes Mindanao
8 Appendicula leytensis Ames house – Orn. Yes Sam-Ley
9 Appendicula malindangensis (Ames) Schltr. 1800–2000 1.5–4 m – Yes Philippines
10 Appendicula cf. pendula Blume 800–900 1.7 m – No Widespread
11 Appendicula undulata var. longicalcarata 650-900 2m Orn. No Widespread
(Rolfe) Ames
12 Appendicula weberi Ames 1150 1.6 m – Yes Philippines
13 Appendicula sp. 1 600–700 1.5 m – – –
14 Appendicula sp. 2 600–700 1.5 m – – –
15 Appendicula sp. 3 800 3–6 m – – –
16 Appendicula sp. 4 800 2m – – –
17 Appendicula sp. 5 1500–1600 1.5 m – – –
18 Blepharoglossum condylobulbon (Rchb.f.) L.Li 800 2.5 m – No Widespread
19 Blepharoglossum grossum (Rchb.f.) L.Li 1600–1800 4m – No Luzon
20 Brachypeza unguiculata (Lindl.) Kocyan & Schuit. 800 2m Orn. No Widespread
21 Bryobium senile (Ames) Schuit. 1600 0.3 m – Yes Philippines
22 Bulbophyllum antenniferum (Lindl.) Rchb.f. 650 2.5 m Orn. No Widespread
23 Bulbophyllum colubrimodum Ames 1370 2m – Yes Philippines
24 Bulbophyllum mucronatum subsp. alagense (Ames) 1400–1600 1.5 m – Nod Philippines
J.J.Verm. & P.O’Byrne
25 Bulbophyllum odoratum (Blume) Lindl. 600–700 2m – No Widespread
26 Bulbophyllum sp. 1 1600–1700 1.7 m – – –
27 Bulbophyllum sp. 2 Sect. Stachysanthes 1300–1400 1.5–2 m – – –
28 Bulbophyllum sp. 3 Sect. Polymeres 1700–1800 5–10 m – – –
29 Calanthe davaensis Ames 1600–1800 Ground – Yes Mindanao

154
Philippine Journal of Science Saavedra and Pitogo: Orchids of Mt. Busa
Vol. 150 No. S1, Special Issue on Biodiversity

Altitudinal distribution Vertical Local Endemism


No. Species Distributionc
(masl)a distribution useb
30 Calanthe cf. furcata Bateman ex. Lindl. 450 Ground Orn. Yes Philippines
31 Calanthe sp. “cf. kinabaluensis” 1500–1600 Ground – – –
32 Cephalantheropsis aff. halconensis (Ames) S.S.Ying 1700–2000 Ground – Yes Philippines
33 Cheirostylis octodactyla Ames 2040 Ground – No Widespread
34 Coelogyne rochussenii de Vriese 400–700 Lithophyte – No Widespread
2m
35 Coelogyne sp. 600–900 2–6 m Orn. – –
36 Corymborkis veratrifolia (Reinw.) Blume 400 Ground – No Widespread
37 Cryptostylis acutata J.J.Sm. 1400–1500 Ground – No Widespread
38 Cryptostylis taiwaniana Masam. 700–800 Ground – No Widespread
39 Cylindrolobus longissimus (Ames & Quisumb.) House – Orn. Yes Luzon
J.J.Wood
40 Cymboglossum cymbidiifolium (Ridl.) Ormerod & 800–1000 2m – No Widespread
Cootes
41 Cystorchis sp. 550 Ground – – –
42 Dendrobium boosii Cootes & W.Suarez 700–1000 2–3 m Orn. Yes Philippines
43 Dendrobium cf. chloranthum Schuit. & Peter House – Orn. Yes Luzon
B.Adams
44 Dendrobium orbilobulatum Fessel & Lückel 1100 4–5 m Orn. Yes Philippines
45 Dendrobium planum J.J.Sm. 500–600 5m – Yes Philippines
46 Dendrobium plicatile Lindl. 1200 1.8 m – No Widespread
47 Dendrobium pterocarpum Ames 1800 7m – Yes Mindanao
48 Dendrobium rhombeum Lindl. 700–1000 10–15 m Orn. Yes Philippines
49 Dendrobium setigerum Ames ex. M.A.Clem 850 10 m – Yes Philippines
50 Dendrobium tiongii Cootes 600–800 2–10 m Orn. Yes Philippines
51 Dendrobium uniflorum Griff. 500–600 2m Orn. No Widespread
52 Dendrochilum coccineum H.A.Pedersen & Gravend. 1700–1800 1.5 m Orn. Yes Mindanao
53 Dendrochilum aff. elmeri Ames 1900–2000 1.5–3 m – Yes Mindanao
54 Dendrochilum glumaceum Lindl. 800 1.6 m – No Widespread
55 Dendrochilum migueldavidii Cootes & Cabactulan 900–1300 1.5–2 m – Yes Mindanao
56 Dendrochilum sp. 1 2000 2m – – –
57 Dendrochilum sp. 2 800 1.7 m – – –
58 Dienia carinata Rchb.f. 1950 Ground – No Widespread
59 Epiblastus merrillii L.O.Williams 1150 3.5 m – Yes Mindanao
60 Epipogium roseum (D.Don) Lindl. 600–700 Ground – Yes Philippines
61 Erythrodes latifolia Blume 700 Ground – Yes Luzon
62 Grammatophyllum wallisii Rchb.f. 400–600 15–20 m Orn. Yes Philippines
63 Lepidogyne longifolia (Blume) Blume 1100-1200 Ground Orn. No Widespread
64 Mycaranthes candoonensis (Ames) Cootes & 1800–2000 2–5 m – Yes Mindanao
W.Suarez
65 Mycaranthes mindanaensis (Ames) Cootes & 1600–1800 2–5 m – Yes Philippines
W.Suarez
66 Oberonia serrulata Schltr. 500–700 2m Orn. No Widespread
67 Octarrhena elmeri (Ames) Ames 550–650 2m – Yes Mindanao
68 Odontochilus marivelensis Ormerod & Cootes 1600–1700 Ground – Yes Philippines
69 Odontochilus yakushimensis (Yamam.) T.Yukawa 2000 2.5 m – No Widespread
70 Oxystophyllum elmeri (Ames) M.A.Clem 800–900 3m – Yes Philippines
71 Paraphaius flavus (Blume) J.W.Zhai, Z.J.Liu & 1700–1800 Ground – Yes Philippines
F.W.Xing

155
Philippine Journal of Science Saavedra and Pitogo: Orchids of Mt. Busa
Vol. 150 No. S1, Special Issue on Biodiversity

Altitudinal distribution Vertical Local Endemism


No. Species Distributionc
(masl)a distribution useb
72 Peristylus goodyeroides (D.Don.) Lindl. 700–900 Ground – No Widespread
73 Phaius tankervilleae (Bank) Blume 600 0.3 m – No Widespread
74 Phalaenopsis mariae Burb.ex R.Warner & House – Orn. Yes Philippines
H.Williams
75 Phalaenopsis reichenbachiana Rchb.f. & Sander 450 4.5 m – Yes Mindanao
76 Phalaenopsis sanderiana Rchb.f. House – Orn. Yes Mindanao
77 Pholidota imbricata Lindl. 400–600 4m Orn. No Widespread
78 Phreatia amesii Kraenzl. 1700 1.5 m – No Widespread
79 Phreatia sulcata (Blume) J.J.Sm. 1800 1.5 m Orn. No Widespread
80 Phreatia sp. 1 1700 1m – – –
81 Phreatia sp. 2 1800–1900 1.5 m – – –
82 Pinalia floribunda (Lindl.) Kuntze 700–1500 1.5–3 m – No Widespread
83 Pinalia nielsenii 1900 1.7 m – Yes Mindanao
Cootes, Cabactulan, & M.Leon
84 Podochilus lucescens Blume House – Orn. No Widespread
85 Podochilus plumosus Ames 1000–1100 2–3 m – Yes Philippines
86 Podochilus sp. 1000–1100 2–3 m – – –
87 Pteroceras longicalcareum (Ames & Rolfe) Garay House – Orn. Yes Philippines
88 Renanthera monachica Ames House – Orn. Yes Philippines
89 Rhomboda lanceolata (Lindl.) Ormerod 1800–2000 0–2 m – No Widespread
90 Robiquetia bifidus (Lindl.) Kocyan & Schuit. House – Orn. Yes Philippines
91 Robiquetia compressa (Lindl.) Schltr. 1400–1600 4m – Yes Philippines
92 Spathoglottis plicata Blume 400–1000 Ground Orn. No Widespread
93 Stichorkis cf. compressa (Blume) J.J.Wood 2000 1.5 m – No Widespread
94 Stichorkis gracilis (Ames) Naive & Ormerod 1600–1700 1.5 m – Yes Philippines
95 Stichorkis leytensis (Ames) Cootes 800–900 2.5 m – Yes Philippines
96 Stichorkis philippinensis (Ames) Naive & Ormerod 1500 1.7 m – Yes Philippines
97 Taeniophyllum philippinense Rchb.f. 2000 1.7 m – Yes Philippines
98 Taeniophyllum sp. 580 1.9 m – – –
99 Thelasis carinata Blume 500–1300 1.5 m – No Widespread
100 Thrixspermum bellamabantae Cabactulan, Cootes & 480 2.5 m – Yes Mindanao
R.B.Pimentel
101 Thrixspermum elmeri L.O.Williams 1950 2m – Yes Negros
102 Thrixspermum merguense (Hook.f.) Kuntze 500 2–2.5 m – No Widespread
103 Thrixspermum rostratum Ames 500 2.5 m Orn. Yes Philippines
104 Thrixspermum sp. 600–700 3m – No –
105 Trichotosia odorifera (Leav.) Kraenzl. House – Orn. Yes Philippines
106 Trichotosia aff. ramosii (Leav.) Kraenzl. 1500–1700 15–20 m – Yes Philippines
107 Vanda cootesii Motes House – Orn. Yes Mindanao
108 Vrydagzynea sp. 1650–1725 Ground – No –
aSpecies that were solely recorded in the villages were denoted as house
bOrn. – species used as ornamental plants
cWidespread – species that are native but not endemic in the Philippines; Philippines – Philippine endemic species that were found in two or more major islands; Luzon

– endemic species that were recorded only in Luzon island; Negros – endemic species that were recorded only in Negros island; Sam-Ley – endemic species that were
recorded only in Samar and Leyte islands; Mindanao – endemic species that are known only to occur in mainland Mindanao.
dThe subspecies is the Philippine endemic

156
Philippine Journal of Science Saavedra and Pitogo: Orchids of Mt. Busa
Vol. 150 No. S1, Special Issue on Biodiversity

Mindoro, and Panay. We also recorded Oberonia serrulata, and 1100 m, although we expect an increase in species
which is a new locality record for the species and the first richness in LMF and UMF (+ 1100 m elevation) with
record for the Philippines (previously known to be endemic in subsequent fieldwork. Several plants we observed in the
New Guinea; confirmed by Ronny Boos and Daniel Geiger). montane forests did not have inflorescence or were past
the flowering stage, making species identification difficult
Most species of orchids were found in the MASLEF (700– or impossible (e.g. species in the genera Ceratostylis,
1100 m elevation) with 39 recorded species, followed by Crepidium, Cylindrolobus, Dendrobium, Trichoglottis,
the UMF (1700–2046 m elevation), LMF (1200–1600 Vanda). Thus, we recommend that fieldwork should cover
m elevation), and MESLEF (400–600 m elevation) with the flowering seasons of various genera to maximize the
28, 20, and 17 recorded species, respectively (Figure 2). species inventory. On the other hand, MESLEF had the
Orchids showed distinct species composition among lowest number of orchid species recorded, but this estimate
forest types, as most species were narrowly distributed. may increase with the addition of new sampling areas.
Only four species occurred in more than two forest The larger area in MASLEF, and the associated environmental
types – namely, Dendrochilum migueldavidii, Pinalia variables that are optimum for many species to survive, could
floribunda, Spathoglottis plicata, and Thelasis carinata. explain the high species richness estimate in this forest
The lowland evergreen forest (MESLEF and MASLEF) type (species-area relationships in mountains; McCain
was mostly composed of species under the genera and Grytness 2010). Our results, although inconclusive at
Appendicula, Dendrobium, and Thrixspermum (each present, suggest a mid-peak in species richness which is
genus had more than two species in this forest type); commonly reported in the literature (Acharya et al. 2011;
the LMF was dominated mainly by Bulbophyllum (four Salas-Morales and Meave 2012; Zhang et al. 2015; Betanio
species) and Calanthe (two species but quite common and Buenavista 2018). However, the elevation at which the
along forest trails in LMF); and the UMF by the genera diversity peaks differs across regions. Orchid diversity in
Dendrochilum, Phreatia, Mycaranthes, Stichorkis, and the mountains in China peak between an elevation of 1300
Appendicula (only A. malindangensis was found in UMF and 1800 m (Acharya et al. 2011; Zhang et al. 2015; Ding
but it was the most abundant). et al. 2016) while mountains in tropical areas peak between
400 and 1000 m (Jacquemyn et al. 2005; Salas-Morales
and Meave 2012; this study). In the Philippines, the forest
between 400 and 1000 m elevation is mostly the tropical
DISCUSSION lowland evergreen, which is the typical rainforest formation
The biodiversity of southern Mindanao has long been in the country (Fernando et al. 2008b).
underrepresented in the scientific literature, as evinced
Species composition also differed among forest types,
by the lack of published studies on biodiversity in the
which may be due to certain traits that allow the species to
region. Our study augments this gap and highlights the
persist at certain elevations (Jacquemyn et al. 2005). This
substantial level of biodiversity in southern Mindanao,
distribution pattern suggests the distinctiveness of each
particularly of the orchidaceous species which are among
forest type in terms of orchid composition highlighting
the most diverse yet threatened groups of plants globally
the importance of encompassing all forest types in
and in the Philippines.
management interventions, as threats differ in kind and
Mount Busa hosts ~ 9% of the country’s estimated number degree across elevation. For instance, the low-elevation
of orchid species and harbors 53+ Philippine endemic forests are hardly hit by habitat degradation (Soh et al.
species. This estimate is higher than other surveyed 2019) and montane organisms at all elevations are affected
montane localities in the Philippines, with twice the by climatic changes as shown in the upward migration of
number of recorded species in previous studies (18–60 mountain plants, causing range contractions of narrowly
species; Panal et al. 2015; Buenavista 2017; Betanio and distributed species (Pauli et al. 1996; Lenoir et al. 2008;
Buenavista 2018). It is even at par with the well-surveyed Bentley et al. 2019).
Samar island that has at least 90 recorded orchid species
Habitat degradation and climatic changes are exacerbated
(Meneses et al. 2018). However, we acknowledge that
by the poaching and harvesting of orchid species, which
differences in species richness estimates could be due to
remain a global threat to orchid populations (Fay 2018;
observer bias and differences in the sampling coverage
Gale et al. 2018). Local collections have been observed in
and effort. Nevertheless, our results foreshadow the high
the villages around Mount Busa for ornamental purposes,
diversity of orchids in southern Mindanao, which is
but we found no evidence yet of trade with outside plant
worthy of conservation attention and further study.
hobbyists and collectors. However, steps to regulate
We recorded the highest orchid species richness in the collection from the wild should be undertaken because all
MASLEF of Mount Busa between an elevation of 700 identified threatened orchids species in Mount Busa have

157
Philippine Journal of Science Saavedra and Pitogo: Orchids of Mt. Busa
Vol. 150 No. S1, Special Issue on Biodiversity

Figure 2. (A) Sample-size-based and (C) coverage-based rarefaction (solid line) and extrapolation (dotted line)
curves for species richness with 95% confidence intervals (shaded areas) for the orchid species recorded in
Mount Busa. The solid triangle represents the reference samples. (B) Sample completeness curve linking
curves in (A) and (C). The curves denote that additional field samplings would still yield more species.

Figure 3. Sample-size-based rarefaction (solid line) and extrapolation (dotted line) curves for species richness with
95% confidence intervals (shaded areas) for the orchid species recorded among different forest types in
Mount Busa. The solid shapes represent the reference samples. LMF – lower montane forest, MASLEF –
mixed advanced secondary lowland evergreen forest, MESLEF – mixed early secondary lowland evergreen
forest, UMF – upper montane forest.

been collected for ornamental use, three of which were diverse orchids in Mount Busa, particularly in the highly
solely observed in the villages (e.g. Phalaenopsis mariae, diverse lowland evergreen forest where access is easier.
Phalaenopsis sanderiana, and Renanthera monachica). It is Species that are range-restricted, endemic, and threatened
for this reason why, as a precaution, we opted not to collect are likewise become vulnerable to poaching.
species for voucher specimens since it might contribute to
the reduction of orchid populations in the wild. Based on Our findings reinforce the Busa Mountain Range as a KBA
our experiences, some locals have the tendency to collect and a high conservation priority site in the Philippines (Ong
any plants that are identified as orchids, so we tried to be et al. 2002). The southern slope of the Busa Mountain
discreet in documenting any orchid species. If poachers Range, where our study sites are situated, has been recently
can penetrate the area then this could threaten the many declared as a local conservation area. Our findings and those

158
Philippine Journal of Science Saavedra and Pitogo: Orchids of Mt. Busa
Vol. 150 No. S1, Special Issue on Biodiversity

Figure 4. Some of the orchid species recorded in Mount Busa: (A) Acanthophippium mantinianum; (B)
Agrostophyllum elongatum; (C) Agrostophyllum loheri; (D) Anoectochilus sp.; (E) Appendicula crotalina;
(F) Appendicula elmeri; (G) Appendicula leytensis; (H) Appendicula malindangensis; (I) Appendicula
cf. pendula; (J) Appendicula undulata var. longicalcarata; (K) Appendicula weberi; (L) Appendicula
sp. 1; (M) Appendicula sp. 2; (N) Appendicula sp. 3; (O) Appendicula sp. 4; (P) Appendicula sp. 5
(Q) Bryobium senile; (R) Bulbophyllum colubrimodum; (S) Bulbophyllum sp. 1; (T) Bulbophyllum
sp. 2; (U) Bulbophyllum sp. 3; (V) Calanthe davaensis; (W) Calanthe sp. “cf. kinabaluensis”; (X)
Cephalantheropsis aff. halconensis; (Y) Cheirostylis octodactyla.

of other studies (Brown 2015; Pitogo 2020) justify this legal southern Mindanao by providing an initial list of orchids
protection, but a designation as a protected area under the in Mount Busa, noting certain ecological traits (i.e.
NIPAS (National Integrated Protected Areas System) may altitudinal and vertical distributions) that are relevant
be required to instigate more conservation and scientific to their conservation and to future studies on orchid
attention given the high level of diversity, endemism, and ecology. We recommend more distribution studies
undescribed species in the area. Many of the KBAs in the of orchids in the Philippines, particularly in montane
Philippines remain unprotected (Mallari et al. 2016), which localities, since the data are needed in many conservation
makes these areas vulnerable to illegal and unsustainable interventions (e.g. monitoring, conservation planning,
activities. Empirical field data offer strong evidence to and species conservation assessments) and help infer
justify protection and facilitate systematic conservation phytogeographical patterns in the country. Ecological
planning (Margules and Pressey 2000). Field-based covariates that influence orchid distribution along
biodiversity studies are particularly relevant in southern environmental gradients should be also explored because
Mindanao, where threats of land conversion, mining, and this information remains scarce for Philippine species.
illegal wildlife trade are becoming rampant. The difficulty of identifying orchid species could hinder
such studies, but the availability of an online platform that
This study provides a step towards strengthening the could connect early-career researchers (ECRs) and experts
protection of one of the last remaining intact forests in

159
Philippine Journal of Science Saavedra and Pitogo: Orchids of Mt. Busa
Vol. 150 No. S1, Special Issue on Biodiversity

Figure 5. Some of the orchid species recorded in Mount Busa: (A) Coelogyne rochussenii; (B) Coelogyne sp.;
(C) Cryptostylis acutata; (D) Cymboglossum cymbidiifolium; (E) Cystorchis sp.; (F) Dendrobium
boosii; (G) Dendrobium cf. chloranthum; (H) Dendrobium orbilobulatum; (I) Dendrobium plicatile; (J)
Dendrobium pterocarpum; (K) Dendrobium rhombeum; (L) Dendrobium setigerum; (M) Dendrobium
tiongii; (N) Dendrochilum coccineum; (O) Dendrochilum migueldavidii; (P) Dendrochilum sp. 1; (Q)
Dendrochilum aff. elmeri; (R) Dendrochilum sp. 2; (S) Dienia carinata; (T) Epiblastus merilii; (U)
Epipogium roseum; (V) Blepharoglossum grossum; (W) Mycaranthes candoonensis; (X) Mycaranthes
mindanaensis; (Y) Oberonia serrulata.

in the field help ameliorate this challenge (see Barcelona and Dan Sulan for their significant contributions to data
et al. 2013). With enough technical support to ECRs, we collection. Tristan Luap Senarillos assisted us in the
may be able to address many long-overdue questions in literature review and John Carlo Redeña Santos created the
Philippine orchidology. map we used in this paper. We appreciate Rene Alfred Anton
Bustamante, Wally Suarez, Ronny Boos, Daniel Geiger,
Jim Cootes, and the many people in the Co’s Digital Flora
of the Philippines Facebook page (and the platform itself)
ACKNOWLEDGMENTS for helping us in the identification. Lastly, we thank the two
anonymous reviewers who have helped in improving the
We recorded the orchid species listed here in the course of
early version of this manuscript.
the Amphibians and Reptiles of Mount Busa project with
financial support from The Rufford Foundation (Project
No. 26752-1), USAID Protect Wildlife, and Idea Wild to
KMP. DENR Region XII provided the permit for fieldwork
(Gratuitous Permit No. 2020-09). We are immensely
REFERENCES
grateful to Lorenzo Sinandon, tribal chieftain of the Tulad ACHARYA KP, VETAAS OR, BIRKS HJB. 2011. Or-
village, for sheltering us and ensuring our safety while chid species richness along Himalayan elevational
on the field. We thank Nestor Gayan, John Timbangan, gradients. Journal of Biogeography 38(9): 1821–1833.

160
Philippine Journal of Science Saavedra and Pitogo: Orchids of Mt. Busa
Vol. 150 No. S1, Special Issue on Biodiversity

Figure 6. Some of the orchid species recorded in Mount Busa: (A) Octarrhena elmeri; (B) Odontochilus marivelensis;
(C) Phalaenopsis mariae; (D) Phalaenopsis reichenbachiana; (E) Phalaenopsis sanderiana; (F) Phreatia
sp. 1; (G) Phreatia sp. 2; (H) Podochilus plumosus; (I) Podochilus sp.; (J) Renanthera monachica; (K)
Rhomboda lanceolata; (L) Robiquetia bifidus; (M) Stichorkis cf. compressa; (N) Stichorkis gracilis; (O)
Stichorkis philippinensis; (P) Taeniophyllum philippinense; (Q) Taeniophyllum sp.; (R) Thelasis carinata;
(S) Thrixspermum elmeri; (T) Thrixspermum merguense; (U) Thrixspermum rostratum; (V) Thrixspermum
sp.; (W) Trichotosia aff. ramosii; (X) Vanda cootesii; (Y) Vrydagzynea sp.

BARCELONA JF, NICKRENT DL, LAFRANKIE JV, BROWN RM, SILER CD, OLIVEROS CH, ESSELTSYN
CALLADO JRC, PELSER PB. 2013. Co’s Digital JA, DIESMOS AC, HOSNER PA, LINKEM CW,
Flora of the Philippines: plant identification and con- BARLEY AJ, OAKS JR, SANGUILA MB, WELTON
servation through cybertaxonomy. Philippine Journal LJ, BLACKBURN DC, MOYLE RG, TOWNSEND
of Science 142: 57–67. PA, ALCALA AC. 2013. Evolutionary processes of
diversification in a model island archipelago. Annual
BENTLEY LK, ROBERTSON MP, BARKER NP. 2019.
Review of Ecology, Evolution, and Systematics 44(1):
Range contraction to a higher elevation: the likely
411–435.
future of the montane vegetation in South Africa and
Lesotho. Biodiversity and Conservation 28: 131–153. BUENAVISTA DP. 2017. Contributions to the orchid flora
of Mindanao Long-term Ecological Research Sites,
BETANIO JMG, BUENAVISTA DP. 2018. Elevational
Philippines. Biologica Nyssana 8(1): 31–38.
pattern of orchid rarity and endemism in Mount Ka-
latungan, Mindanao island, Philippines. Journal of CABACTULAN DD, COOTES J, DE LEON MD, PI-
Tropical Life Science 8(2): 108–115. MENTEL RB, AURIGUE FB, BINAYAO III NK.
2018. Nineteen new orchid species from northern
BROWN RM. 2015. A new species of stream frog of the
Mindanao, Philippines. Orchideen Journal 6: 1–21.
genus Hylarana from the mountains of southern Mind-
anao island, Philippines. Herpetologica 71(3): 223–233.

161
Philippine Journal of Science Saavedra and Pitogo: Orchids of Mt. Busa
Vol. 150 No. S1, Special Issue on Biodiversity

CLEMENTS M, COOTES J. 2009. The systematics of GRAVENDEEL B, SMITHSON A, SLIK FJ, SCHUITE-
the Orchidaceae for flora Malesiana II: Miscellaneous MAN A. 2004. Epiphytism and pollinator special-
Dendrobieae from the Philippines. Orchideen Journal ization: drivers for orchid diversity? Philosophical
16:19–27. Transactions of the Royal Society of London. Series
B: Biological Sciences 359(1450): 1523–1535.
COOTES JE. 2001. A Selection of Orchids from the
Philippines. Portland: Timber Press, Inc. HALL R. 2002. Cenozoic geological and plate tectonic
evolution of SE Asia and the SW Pacific: computer-
COOTES JE. 2011. Philippine Native Orchid Species. Que-
based reconstructions, model and animations. Journal
zon City, Philippines: Katha Publishing Co., Inc. 289p.
of Asian Earth Sciences 20(4): 353–431.
DE LEON MD, NAIVE MA, COOTES J. 2017. A new
HINSLEY A, DE BOER HJ, FAY MF, GALE SW, GAR-
Ceratostylis (Orchidaceae) species from Bukidnon,
DINER LM, GUNASEKARA RS, KUMAR P, MAS-
Philippines. Phytotaxa 305(4): 299–300.
TERS S, METUSALA D, ROBERTS DL, VELDMA-
[DENR] Department of Environment and Natural Re- NS, WONG S, PHELPS J. 2017. A review of the trade in
sources. 2017. Updated national list of threatened orchids and its implications for conservation. Botanical
Philippine plants and their categories. DENR Admin- Journal of the Linnean Society 186(4): 435–455.
istrative Order No. 2017-11. 30p.
HUNDERA K, AERTS R, DE BEENHOUWER M, VAN
DING Y, LIU G, ZANG R, ZHANG J, LU X, HUANG OVERTVELD K, HELSEN K, MUYS B, HONNAY
J. 2016. Distribution of vascular epiphytes along a O. 2013. Both forest fragmentation and coffee cul-
tropical elevational gradient: disentangling abiotic tivation negatively affect epiphytic orchid diversity
and biotic determinants. Scientific Reports 6: 19706. in Ethiopian moist evergreen Afromontane forests.
Biological Conservation 159: 285–291.
FAY MF. 2015. Undocumented trade in species of Orchida-
ceae. Retrieved on 09 Aug 2020 from https://cites.org/ HSIEH TC, MA KH, CHAO A. 2016. iNEXT: an R
sites/default/files/eng/com/pc/22/Inf/E-PC22-Inf-06.pdf package for rarefaction and extrapolation of species
diversity (Hill numbers). Methods in Ecology and
FAY MF. 2018. Orchid conservation: how can we meet
Evolution 7: 1451–1456.
the challenges in the twenty-first century? Botanical
Studies 59: 16. JACQUEMYN H, MICHENEAU C, ROBERTS DL,
PAILLER T. 2005. Elevational gradients of species
FERNANDO ES, CO D, LAGUNZAD D, GRUEZO W,
diversity, breeding system and floral traits of orchid
BARCELONA J, MADULID D, LAPIS A, TEXON
species on Reunion Island. Journal of Biogeography
G, MANILA A, ZAMORA P. 2008a. Threatened plants
32(10): 1751–1761.
of the Philippines: a preliminary assessment. Asia Life
Sciences Supplement 3: 1–52. LENOIR J, GEGOUT JC, MARQUET PA, DE RUF-
FRAY P, BRISSE H. 2008. A significant upward shift
FERNANDO ES, SUH MN, LEE J, LEE DK. 2008b.
in plant species optimum elevation during the 20th
Forest formation of the Philippines. ASEAN – Korea
century. Science 320: 1768–1771.
Environmental Cooperation Unit (AKECU). Seoul:
GeoBook Publishing Co. 192p. MALLARI NAD, COLLAR NJ, MCGOWAN PJ,
MARSDEN SJ. 2016. Philippine protected areas are
GALE SW, FISCHER GA, CRIBB PJ, FAY MF. 2018.
not meeting the biodiversity coverage and management
Orchid conservation: bridging the gap between science
effectiveness requirements of Aichi Target 11. Ambio
and practice. Biological Journal of Linnean Society
45(3): 313–322.
186(4): 425–434.
MARGULES CR, PRESSEY RL. 2000. Systematic
GOVAERTS R, BERNET P, KRATOCHVIL K, GER-
conservation planning. Nature 405(6783): 243–253.
LACH G, CARR G, ALRICH P, PRIDGEON AM,
PFAHL J, CAMPACCI MA, HOLLAND BAPTISTA D, MCCAIN CM, GRYTNESS JA. 2010. Elevational gradi-
TIGGES H, SHAW J, CRIBB P, GEORGE A, KREUZ ents in species richness. Encyclopedia of Life Sciences
K, WOOD J. 2020. World Checklist of Orchidaceae. Fa- (ELS). Chichester: John Wiley & Sons, Ltd. 10p.
cilitated by the Royal Botanic Gardens, Kew. Retrieved
MENESES ZD, COOTES JE. 2019. Pseuderia samarana
on 21 Aug 2020 from http://wcsp.science.kew.org/
(Orchidaceae), a new species and genus record from
GUO YY, LUO YB, LIU ZJ, WANG XQ. 2015. Reticulate the Philippines. Taiwania 64(4): 353–356.
evolution and sea‐level fluctuations together drove spe-
cies diversification of slipper orchids (Paphiopedilum) in
South-East Asia. Molecular Ecology 24(11): 2838–2855.

162
Philippine Journal of Science Saavedra and Pitogo: Orchids of Mt. Busa
Vol. 150 No. S1, Special Issue on Biodiversity

MENESES ZD, MALABRIGO PL JR., BUOT IE JR., SALAS-MORALES SH, MEAVE JA. 2012. Elevational
TINIO CE. 2018. New distribution records of orchids patterns in the vascular flora of a highly diverse region
(Orchidaceae) in Samar island, Philippines. Journal of in southern Mexico. Plant Ecology 213(8): 1209–1220.
Nature Studies 17(2): 1–9.
SOH MCK, MITCHELL NJ, RIDLEY AR, BUTLER CW,
NAIVE MAK, MARTYR JC. 2018. Trichoglottis cora- PUAN CL, PEH KS, ADAMS MA. 2019. Impacts of
zoniae (Orchidaceae: Vandeae: Aeridinae), a new spe- habitat degradation on tropical montane biodiversity
cies from the Philippines. Lankesteriana 18(2): 81–84. and ecosystem services: a systematic map for identify-
ing future research priorities. Frontiers in Forest and
NAIVE MAK, COOTES J, ORMEROD P. 2019. Stichorkis
Global Change 2(83): 1–18.
davidlohmanii (Orchidaceae; Malaxideae), a new species
from the southern Philippines. Taiwania 64(1): 65–68. TAMAYO MN, MC ANDREW KP, BUSTAMANTE
RAA. 2020. Dendrochilum ignisiflorum (Coelogy-
ONG PS, AFUANG LE, ROSELL-AMBAL RG. 2002.
ninae, Arethuseae, Orchidaceae), a new species from
Philippine Biodiversity Conservation Priorities: A
Luzon Island, Philippines. Phytotaxa 455(4): 240–244.
Second Iteration of the National Biodiversity Strategy
and Action Plan. Quezon City, Philippines: Department TANDANG DN, GALINDON JMM, TADIOSA ER,
of Environment and Natural Resources- Protected CORITICO FP, AMOROSO VB, LAGUNDAY NE,
Areas and Wildlife Bureau, Conservation International BUSTAMANTE RAA., PENNEYS DS, FRITSCH
Philippines, Biodiversity Conservation Program-Uni- PW. 2020. Dilochia deleoniae (Orchidaceae), a new
versity of the Philippines Center for Integrative and species from Mindanao, Philippines. PhytoKeys 139:
Development Studies, and Foundation for the Philip- 91.
pine Environment. 113p.
TSAI CC, CHOU CH, WANG HV, KO YZ, CHIANG TY,
PANAL CLT, OPISO JG, OPISO G. 2015. Conservation CHIANG YC. 2015. Biogeography of the Phalaenop-
status of the Family Orchidaceae in Mount Sinaka, sis amabilis species complex inferred from nuclear and
Arakan, North Cotabato, Philippines. Biodiversitas plastid DNAs. BMC Plant Biology 15: 202.
16(2): 213–324.
TSAI CC, LIAO PC, KO YZ, CHEN CH, CHIANG
PARRA SANCHEZ E, ARMENTERAS D, RETANA J. YC. 2020. Phylogeny and historical biogeography of
2016. Edge influence on diversity of orchids in Andean Paphiopedilum Pfitzer (Orchidaceae) based on nuclear
cloud forests. Forests 7(3): 63. and plastid DNA. Frontiers in Plant Science 11: 126.
PAULI H., GOTTFRIED M, GRABHERR G. 1996. YUMUL GP, DIMALANTA CB, TAMAYO RA, MAURY
Effects of climate change on mountain ecosystems– RC, BELLON H, POLVE M, MAGLAMBAYAN VB,
upward shifting of alpine plants. World Resource QUERUBIN CL, COTTEN J. 2004. Geology of the
Review 8(3). Zamboanga Peninsula, Mindanao, Philippines: an enig-
matic South China continental fragment? Geological
PELSER PB, BARCELONA JF, NICKRENT DL. 2011
Society, London, Special Publications 226: 289–312.
onwards. Co's Digital Flora of the Philippines. Re-
trieved on May 2020 from www.philippineplants.org ZHANG SB, CHEN WY, HUANG JL, BI YF, YANG
XF. 2015. Orchid species richness along elevational
PITOGO KME. 2020. Amphibians and reptiles in Mount
and environmental gradients in Yunnan, China. PLoS
Busa, Sarangani, Philippines: species distribution in
One 10(11): e0142621.
a tropical forest gradient [MS Thesis]. University of
the Philippines Los Baños. 139p. (Available at the
UPLB Library)
R CORE TEAM. 2020. R: A language and environment
for statistical computing. R Foundation for Statistical
Computing, Vienna, Austria. Retrieved on 05 Sep 2020
from https://www.R-project.org/
SAJONA FG, BELLON H, MAURY RC, PUBELLIER
M, QUEBRAL RD, COTTEN J, BAYON FE, PAGA-
DO E, PAMATIAN P. 1997. Tertiary and quaternary
magmatism in Mindanao and Leyte (Philippines):
geochronology, geochemistry and tectonic setting.
Journal of Asian Earth Sciences 15(2–3): 121–153.

163

You might also like