Journal of Threatened
Taxa | www.threatenedtaxa.org | 26 November 2022 | 14(11): 22039–22057
ISSN 0974-7907
(Online) | ISSN 0974-7893 (Print)
https://doi.org/10.11609/jott.7640.14.11.22039-22057
#7640 | Received 01
September 2021 | Final received 20 September 2022 | Finally accepted 25 October
2022
New records of pteridophytes in
Mount Matutum Protected Landscape, South Central Mindanao, Philippines with
notes on its economic value and conservation status
Christine Dawn Galope-Obemio
1, Inocencio E. Buot Jr.
2 & Maria Celeste
Banaticla-Hilario 3
1 Science Department, College of
Natural Sciences and Mathematics, Mindanao State University-General Santos
City, Fatima, General Santos City 9500, Philippines.
2,3 Plant Biology Division, Institute
of Biological Sciences, University of the Philippines Los Baños College,
Laguna 4031, Philippines.
1 christinedawn.obemio@msugensan.edu.ph
(corresponding author), 2 iebuot@up.edu.ph, 3 mbhilario1@up.edu.ph
Editor: K.P.
Rajesh, The Zamorin’s Guruvayurappan College (affiliated to University of
Calicut), Kozhikode, Kerala, India. Date of publication: 26 November
2022 (online & print)
Citation: Galope-Obemio, C.D., I.E. Buot
Jr. & M.C. Banaticla-Hilario (2022). New records
of pteridophytes in Mount Matutum Protected Landscape, South Central Mindanao,
Philippines with notes on its economic value and conservation status. Journal of Threatened Taxa 14(11): 22039–22057. https://doi.org/10.11609/jott.7640.14.11.22039-22057
Copyright: © Galope-Obemio et al. 2022. 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) Department of Science and Technology-Philippine Council for Agriculture,
Aquatic and Natural Resources Research Division (DOST-PCAARRD) United States
Agency for International Development (USAID) Protect Wildlife Project.
Competing interests: The authors declare no competing
interests.
Author details: Christine Dawn
Galope-Obemio is an assistant
professor of Plant Biology at the Science Department, College of Natural
Sciences and Mathematics, Mindanao State University-General Santos City, Philippines.
She also serves as a coordinator for the graduate program in biology of the
university. She specializes in
floristics, fern systematics and ecology, biodiversity, and conservation. Inocencio
E. Buot Jr is a professor of botany, ecology and systematics at the
Plant Biology Division, Institute of Biological Sciences, University of the
Philippines Los Baños. He curates the Plant Biology Division Herbarium and
leads research on vegetation of Philippine mountains and on leaf architecture
studies of vascular plants, resolving taxonomic confusion of some controversial
taxa. Maria Celeste Banaticla-Hilario
is an assistant professor of systematics at the Plant Biology Division,
Institute of Biological Sciences, University of the Philippines-Los Baños. Her
research interest is on, plant systematics, biodiversity, conservation, crop
evolution and ecogeography. She mentors
students in the field of biosystematics, floristics, biodiversity, and
conservation
Author contributions: Christine Dawn Obemio lead author.
Assisted in the study conception and design, collected, analyzed data,
interpreted the results and drafted the manuscript. Inocencio E. Buot, Jr. led
the study conception and design. Assisted in the analysis of data and
interpretation of results. Reviewed the draft manuscript and added critically
important intellectual content. Maria Celeste Banaticla-Hilario assisted in
study conception and design, analysis of data and interpretation of results and
drafting the manuscript. Reviewed the draft manuscript and organized the flow
of the discussion.
Acknowledgements: The authors would like to thank
the Protected Area Superintendent (PASu) office of the Department of
Environment and Natural Resources (DENR), South Cotabato, the Protected Area
Management Board (PAMB) of Mount Matutum Protected Landscape, the Municipal
Environment and Natural Resources Officer of Tupi and Polomolok, South
Cotabato, the Municipal and Barangay Local Government Units (Barangay Glandang,
Tupi, South Cotabato, and Barangay Palkan, Polomolok, South Cotabato), for
their support in this study by granting the necessary permits, guiding the
researchers before and during the conduct of the study and providing personnel
assistance. This study will not also be possible without the help of the local
community guides who led in navigating the protected area and our field
assistants, Aljohn Jay Saavedra, and Henry Earl Tayco who aided in the
collection and storage of samples. Gratitude is also given to the Commission on
Higher Education (CHED), the Department of Science and Technology-Philippine
Council for Agriculture, Aquatic and Natural Resources Research and Development
(DOST-PCAARRD) and Protect Wildlife for providing grant assistance.
Abstract: New records on distribution of
pteridophytes in Mount Matutum Protected Landscape were documented. The species
list was accounted with reference to specimen collections from various herbaria
posted in digital databases and reliable literature on pteridophyte flora.
Results further showed 105 new records for MMPL and its vicinity-South
Cotabato, Sarangani province and General Santos City. From these, seven
were new records for South Central Mindanao Region (Region 12). About 19
families, 56 genera were represented – 41 were epiphytes, 10 lithophytes, and
45 soil inhabitants, the rest with dual habits – two (ground and lithophytic);
seven (epiphytic and lithophytic). Moreover, 11 species were found to be
threatened based on national list while local conservation assessment based on
relative frequency noted 91 threatened species. A conservation plan for
these valuable species in the protected landscape is also proposed to ensure
sound intervention and sustainable environment for this plant group.
Keywords: Ferns, General Santos,
lycophytes, Matutum, protected area, Sarangani, South Cotabato.
INTRODUCTION
A significant understory flora
growing in the forest reserves are the pteridophytes or the ferns and
lycophytes. These plants are widely distributed both in the tropical and
temperate regions especially at higher elevations, and they flourish in moist,
shaded habitats (Delos Angeles & Buot 2012). They are known to have high
economic value as ornaments, food, and medicine, and are noted for its high
ecological importance as indicators of environmental quality (Pouteau et al.
2016; Silva et al. 2018; Khine et al. 2019). Pteridophytes are also host to
diverse faunal species (Ellwood & Foster 2004; Beaulieu et al. 2010;
Scheffers et al. 2014). However, its richness and diversity are continuously
challenged by geogenic and anthropogenic factors that lead to fragmentation and
decrease in species over the years (Rodriguez et al. 2011; Silva et al. 2018).
It is then very important to know the floristics of pteridophytes in the
landscape to have a better understanding on appropriate conservation
interventions.
The majestic Mount Matutum
Protected Landscape (MMLP) in the South Cotabato, Sarangani and General Santos
(SOCSARGEN) region of southern Mindanao, is an important source of pteridophyte
diversity. In fact, the entire island of Mindanao has been explored for
pteridophyte diversity and about 186 species were identified (Hassler
2004----2022). Meanwhile, 11 species were described and named bearing the
epithets of mindanaoensis, mindanensis or mindanaense – Adiantum
mindanaense, Alsophila mindanensis, Cyclosorus mindanaensis, Thelypteris
mindanaensis, Microsorum mindanense, Polypodium mindanense, Polypodium
punctatum ssp. mindanense, Polypodium punctatum var. mindanense,
Selaginella mindanaoensis, Tectaria mindanaensis, and Aenigmopteris
mindanaensis (Hassler 2004-2022). Though all of these except A.
mindanaense were already considered synonyms, it still highlights the
significant flora in this southern part of the country.
Mount Matutum was declared as
protected area in 1995 through the Presidential Proclamation 552, and included
in the rooster of Key Biodiversity Areas (KBAs) (Conservation International -
Philippines, Haribon Foundation and the Department of Environment and Natural
Resources) and Important Bird Areas (IBAs) (Birdlife International 2018) making
it a priority site for conservation. It holds forest wealth of significant
flora, largely unexplored that could potentially be lost together with the
ecosystem services they provide, with influx of population in the surrounding
communities.
Scientific studies on Mt.
Matutum’s biodiversity have been scarce with only a handful published accounts
on trees (Obemio et al. 2016), and bryophytes (Azuelo et al. 2016). Similarly,
assessments on its faunal resource were limited to anurans (Nuñeza et al.
2017a), reptiles (Nuñeza et al. 2017b), avians (Nuñeza et al. 2019), and bats
(Nuñeza et al. 2015). Until this time, these remained the only published
accounts for Mt. Matutum.
Interestingly, the earliest
pteridophyte exploration in the protected area dates back to more than a
hundred years ago (1917) by Copeland where he observed about 99 species. Among
these, Gleichenia peltophora and Diplazium calliphyllum are known
in the Philippines from this site only. Also, three species, though currently treated as
synonyms, were named after the landscape, namely, Ctenopteris matutumensis,
Dryopteris matutumensis, and Selliguea matutumensis. However,
a concerted effort on documenting the Pteridophyte flora of the area remains
unfinished.
The present attempt is thus the
first of its kind in collating the details from various sources, including data
from various herbaria and on recent field studies. It also seeks to present the
economic uses associated with the pteridophytes and develop a local
conservation status for each as many were not yet assessed with reference to
the threatened list by the International Union for the Conservation of Nature
(IUCN). As this study is the first attempt to document a more comprehensive
account of the pteridophytes in the protected area, a lot of species then are
new records for Mount Matutum and its vicinity – south central Mindanao region.
The feature of these species is a remarkable milestone for MMPL and a
significant step towards strengthening conservation interventions in the
protected area. The authors seek to address the gap of an updated floristics
and new records of pteridophytes in MMPL that would be crucial in their
integration to conservation management as they are inevitably part of the
ecosystem and function to enhance stability, resiliency, and sustainability of
the landscape. This in turn cascade to the communities in form of ecosystem
services, highlighting its conservation value.
MATERIALS AND METHODS
Study Area
Mount Matutum Protected Landscape
(MMPL) is an important landmark and ecological watershed of South Cotabato and
Sarangani Provinces in Southern Mindanao. It is surrounded by four
municipalities (three in South Cotabato; one Sarangani Province) and 14
barangays (12 South Cotabato, two Sarangani Province). A stratovolcano, this landscape stands to
about 2,286 m, covering an approximate area of 14,000 ha of forestland, with
3,000 ha of a primary forest. A
community of vascular (trees, pines, ferns) and non-vascular (mosses, liverworts,
hornworts) plants thrive in this this primary forest.
The climate in the northwestern
and southwestern parts of this protected area is tropical with significant
rainfall throughout the year even in the driest months. It is classified as
Type IV with reference to Philippine-climate types and tropical wet (Af
category) based on the worldwide Köppen-Geiger. Monthly temperature variations
are no greater than three degrees Celsius characterized by intense surface
heating and high humidity resulting to daily formation of cumulus and
cumulonimbus. These conditions favor the growth of different kinds of ferns and
fern allies, which greatly prefer shaded and damp habitats. Moreover, the presence of rocky environments,
slopes, and host trees make this landscape a host to diverse species of
pteridophytes.
Field Methods
Assessment was done following the
method of Banaticla & Buot (2004) and Delos Angeles & Buot (2015). A
line transect of 10─20 m, depending on the heterogeneity of pteridophyte
patches, was established. At least one transect was assessed for every 100 m
elevation range. All fern and lycophytes along the transect were documented
including epiphytes observed below 2.5 m.
Two sites in MMPL were considered
as study areas to represent its northwestern slope (Image 1). Site 1 was in the
municipality of Tupi, South Cotabato, accessible through the Glandang Trail
(6.35050N, 125.05700E) while site 2 was in the
municipality of Polomolok, South Cotabato, around the Keumang-Alnamang trail
(6.33000N, 125.06050E).
A total 92 transects were
subjected for sampling, Site 1 with 52 and Site 2 with 40 transects.
Composition of ferns and fern allies were listed in every transect. Voucher
specimens were collected in duplicate to triplicate whenever possible.
Geographic location and elevation were determined using a geographic
positioning system (GPS) device.
Laboratory Methods
Voucher preparation and
identification
Collected specimens from MMPL
were pressed and mounted in herbarium sheets. The herbarium specimens were
stored, labeled, and prepared for distribution in Mindanao State
University-General Santos City and Plant Biology Division, Institute of
Biological Sciences, UPLB herbaria. Taxonomic identification and determination
of distribution records were done using relevant taxonomic literature - Copeland
(1958) and online databases (Pteridoportal:
https://www.pteridoportal.org/portal/index.php, Co’s Digital Flora:
https://www.philippineplants.org/, Ferns of the World:
https://www.fernsoftheworld.com/). Experts in the field – Barbara Parris (Fern
Research Foundation), Fulgent Coritico (Central Mindanao University, Bukidnon,
Northern Mindanao), Cherie Cano (University of Southern Mindanao, Kabacan,
North Cotabato), were also consulted to validate the specimen identification.
Based on these the new records, new distribution and rediscovered pteridophyte
species in Mount Matutum and its vicinity - surrounding provinces of South
Cotabato, Sarangani Province and city of General Santos were identified.
New records were evaluated and
described with reference to relevant literature and database information. Key
literature were the Fern Flora of the Philippines (Copeland 1958), and others
such as Ebihara et al. (2006), Lehtonen et al. (2013), Parris & Sundue
(2020). Database searches were also made through Cos Digital Flora of the
Philippines (Pelser et al. 2011 in www.philippineplants.org), Catalogue of Life
(Species 2020) (www.catalogueoflife.org), Flora of China (www.efloras.org) and
Pteridoportal (Pteridophyte Collections Consortium) (www.pteridoportal.org)
World Ferns (Hassler 2004─2022) and Flora Malesiana – www.floramalesiana.org
(accessed 27 April 2018).
The conservation status of new
records was determined from International Union for the Conservation of Nature
(IUCN) Threatened List version 2021 from www.iucn.org, and the Department of
Environment and Natural Resources (DENR) Administrative Orders (DAO) 2017─11
which features the Updated List of Threatened Philippine Plants and their
Categories.
Local Conservation Assessment
Local assessment of conservation
was done using the relative frequency of species distribution in MMPL with
reference to the work of Villanueva and Buot (2020). Relative frequency (RF)
was determined by the ratio of the number of transects where the species were
observed and the total number of transects. Frequency below < 0.1% was
considered critically endangered (CR), > 0.1 – 0.4% endangered (EN), >
0.4 – 0.7 vulnerable (VU), 0.7 -1 nearly threatened (NT), and > 1 least
concerned (LC). This local assessment highlighted the conservation status of
those species found in MMPL that were not yet assessed in IUCN nor identified
in DAO (2017─11).
RESULTS AND DISCUSSION
New Records in Mount Matutum
Protected Landscape (MMPL)
Earlier studies recorded about
160 pteridophytes in Mount Matutum (Copeland 1917; Gaerlan et al. 1992;
Gonzales 2001; Mindanao State University-General Santos City 2013), while this
present undertaking adds another 105 taxa, totaling to 265 species in the Matutum
area. Of these, 12 were lycophytes while
93 were monilophytes (ferns). As to habit, 45 were terrestrial, 41 epiphytes,
10 lithophytes and the rest showed dual habits such as terrestrial &
lithophytic (two species) and epiphytic & lithophytic (seven species)
(Table 1).
Copeland (1917) observed 57 ferns
which were highlighted in his work on Fern Flora of the Philippines.
Seventy-five years later, Gaerlan et al. (1992) collected 24 species as part of
the biodiversity inventory of Philippine National Musuem. The next assessment
was done in 2001 by Dr. Gonzales which showed 188 species and so far, the
largest collection prior to this study. Meanwhile, MSU-GSC did an assessment in
the lowland forest in 2013 and enlisted about 42 species. The works of Dr.
Gonzales and MSU-GSC were unpublished records.
On the opposite side of MMPL, in
Mount Busa, Kiamba, Sarangani Province, about 114 pteridophytes were observed
from the exploration by Barcelona & Busemeyer (1993) based on digitized
herbarium specimen collections from Miami University, Willard Sherman Turrell
Herbarium (MU) and National Museum of Natural History-US Botany published in
Pteridophyte Collections Consortium (www.pteridoportal.org). Meanwhile, in the
Allah Valley Protected Landscape, northern part of MMPL, no records of
pteridophytes have been known yet.
Interesting new records are the Athyrium
nakanoi, Athyrium puncticaule, Calymmodon gracillimus, Dicksonia
amorosoana, Diplazium geophilum, Dryopteris purpurascens, Oreogrammitis
jagoriana, Oreogrammitis reinwardtii, Prosaptia multicaudatum,
Prosaptia celebica, Sphaerostephanos ellipticus, as they are the
first or second occurrence report in the region or Mindanao. Mt. Matutum holds
the second record so far in the country for A. nakanoi and D.
amorosoana. A. nakanoi used to be documented in India, Nepal,
Bhutan, China, Taiwan, Japan, Indonesia, and Malaysia and was first seen in the
country in Mount Dulang-dulang Kitanglad Range, northern Mindanao (Coritico et
al. 2019). The tree fern D. amorosoana on the other hand, is a recently
described narrow endemic species of Dicksonia from the Philippines,
first observed in Mount Apo, Kidapawan, North Cotabato, Mindanao (Lehnert &
Coritico 2018). Its second distribution record is in MMPL and to date, occurrence
is confined to South Central Mindanao (Region 12). Abundance in MMPL of these
species is marked as rare with < 5 species and frequency data of < 10%.
The species C. gracillimus,
O. reinwardtii, and O. jagoriana are noteworthy records of
grammitid ferns as they are not only new observations in MMPL and surrounding
provinces, but also new for Region 12. They were last observed in 1904 &
1909 and 1904 & 1924, respectively, in Mount Apo and Davao Region (www.pteridoportal.org,
www.worldplants.de/worldferns). Similarly, S. ellipticus an endemic
fern, is a new record for the region with type specimens found in Mindanao –
Agusan & Zamboanga, from 1911─1912 collections (www.pteridoportal.org).
Also forming the new records for
South Central Mindanao are Asplenium laserpitiifolium, D. geophilum, P. multicaudatum and P. celebica which
were all observed in the montane forest of MMPL. There were also ferns
discovered by E. Copeland in 1917 which at that time were second occurrence
records in the entire Philippines ― Sphaerostephanos urdanetensis,
Cornopteris opaca, Cornopteris philippinensis. Meanwhile, based on
worldwide database for herbarium collections, two species in Mount Matutum recorded by Copeland
in 1917 remained to be the only record so far in the country namely G.
peltophora and Diplazium calliphyllum.
These new records in MMPL provide
significant contribution to the biodiversity heritage of Mindanao island. Prior
to this study, published accounts on pteridophyte diversity has largely been
from two regions ― 10 (Mt. Malindang & Mt. Kitanglad Range in Bukidnon) and
11 (Mt. Hamiguitan Range). The highest richness reported here was in Mt.
Kitanglad Range which totalled to 439 with a total account of 632 species for
the entire Mindanao island (Amoroso et al. 2011). It is expected then that the
account on species richness will change with the results from this study.
Several species were also
highlighted as useful either as medicine, food, or ornamental (Table 2). Tree ferns (Alsophila, Sphaeropteris)
have been used as source of starch in Hawaii (Ripperton 1924; May 1978; Leach
2003) while in India it is sought from stems of giant ferns Angiopteris
(Liu et al. 2012). Starch is an
important product worldwide used for different purposes – preservative, thickening
agent, food enhancer and stabilizer and key ingredients in pastas, soups,
sauces (Mason 2009; Egharevba 2019).
Fern starch has been used as additive along with rice, potato and corn
flour in the production of liquor and soft drinks (Liu et al. 2012). Meanwhile,
fats from rhizomes have been extracted from Dryopteris which contains
90% monoethenoid (unsaturated) acids (May 1978).
Medicinal ferns have been used
since ancient times for common diseases ― gastric, inflammatory, infections,
because of the ethnobotanical knowledge on their potential as antibacterial,
anti-inflammatory, diuretics and pain killers passed on to generations (Ho et
al. 2010). Medicinal value was identified in Lycopodium clavatum,
Selaginella involvens, Angiopteris evecta, Christella dentata, Asplenium
cuneatum, and Dryopteris species while ornamental uses were featured
in several Asplenium, Adiantum and, Drynaria species, and
in Odontosoria chinensis and Pseudodiphasium volubile (Table 2).
On the other hand, ornamental ferns have been sought to provide aesthetic value
for the enjoyment of the public and potentially for environmental protection
and management (Oloyede 2012) and interestingly, more money is spent for this
than for all other uses (May 1978).
Notable from the list of new
records is L. clavatum having been widely documented for medicinal
purposes. It has been known as emetic for stomach disorders (Srivastava 2007),
cure for kidney and lung diseases, analgesic, antioxidant, anti-cancer,
anti-inflammatory, neuroprotective, immunomodulatory, and hepatoprotective
(Bhardwaj & Misra 2018). It was also explored as potent treatment for
learning and memory impairment (Hanif et al. 2015). It is diuretic and
anti-spasmatic and also smoked with Selaginella rupestris to cure
headaches (Watt & Brandwijk 1962). In Sweden, L. clavatum is also
woven into mats (May 1978).
The checklist of new records for
MMPL highlights the significance of the landscape as biodiversity area in South
Central Mindanao. It confirms the favorable microenvironment brought about by
stable ecosystem processes in the landscape (MMPL), thereby able to house
unique plants, enhancing the natural heritage. The discovery of these new
records after more than 100 years, is a significant achievement, realizing that
there had been few explorations in between then and now. Moreover, knowledge of
species occurrence is crucial to biodiversity conservation as this provides
basis for scientific-based efforts to restore diversity at its different levels
(Pavlik 1995; Mehltreter 2010; Cutko 2009; Green et al. 2009; Weigelt et al.
2019). It is perceived that this study would jumpstart the continuous and
regular monitoring and inventory of pteridophytes in order to aid planning, management,
and policy development for the protected area. This would further lead to the
inclusion of MMPL pteridophyte flora in national and worldwide botanical data
and provide extensive compilation of geographic species at regional, national,
and global levels.
The discovery of many economic
uses of ferns and lycophytes is very instrumental to raising awareness and
appreciation on the utilitarian values of this plant group. Studies to
elucidate the bioactive products found in its various plant parts have led to
its integration in drug discovery and potential use for various chronic and
infectious diseases (Ho et al. 2010; Baskaran et al. 2018). Likewise, its
ornamental values serve a pivotal role in environmental protection and
management interventions and can be harnessed to improve environmental
landscapes (Oloyede 2012). As the country is among the richest in pteridophyte
diversity in Asia, avenues for expanding current knowledge on their utilitarian
as well as ecological values are numerous, waiting to be explored.
Conservation status of the new
records
With reference to IUCN Threatened
List 2021, it can be grasped that all new records in MMPL belong to the Not
Assessed (NA) category. The DAO-2017-11 of DENR is another reference which also
integrated the national red list of threatened species (in reference to IUCN)
developed in 2008 by Fernando et al. (2008). From this, a total of 11 species
from new records were in the threatened category. The rest belong to other wildlife species
(OWS) which refers to the native species in the landscape that were not
classified to any of the threatened category. Meanwhile, seven of these new
records were found to be endemic, confined only in the country.
Local assessment tool based on
the relative frequency values showed a different picture as many of the OWS in
DAO were placed in threatened category (Table 3). From the NA of IUCN, the OWS of DAO and
native species which is roughly the least-concerned at national, and global levels,
20 were classified under CR, 44 under EN, sixVU and nine NT. Only nine species were noted to be relatively the same
with least concerned status. Meanwhile, from the not threatened but endemic
species (NA in IUCN, OWS in DAO and Endemic), two were found to be CR, three EN
and one VU.
Under the threatened and native
species category (NA in IUCN, threatened in DAO, native), one was found as CR,
three were endangered, two vulnerable,
one NT and four were LC. Further, the threatened and endemic category enlisted
one VU and three LC species.
The local conservation status
developed in this study is a simple categorical classification intended to have
an immediate reference for conservation priority of pteridophyte species in
MMPL. It is a vital alternative in the absence of data from IUCN which
generally considers global distribution of high-valued plant species
(Langenberger 2006; Villanueva & Buot 2020). As can be drawn from this
study, the new records in MMPL were not yet assessed in IUCN except for one
species, Sphaeropteris glauca, which was classified as least concerned.
Some were also highlighted in the national list DAO 2017─11. The use of
relative frequency scores could serve as reliable representation of the
species’ adaptation, higher RF as widely-adapted while low RF values depict restricted-range
species. It is significant as in the case of MMPL which needs immediate
reference as scientific information is scarce. Moreover, it can be modified in
the future to include other factors that may influence their diversity and
distribution such as harvest use, economic uses, threats, and other ecological
factors similar to those highlighted in several works (Bacchetta et al. 2012;
Rana et al. 2020; Villanueva & Buot 2020).
High priority species based on
local assessment along with their endemicity and threatened status at the
national level (DAO 2017─11) would serve as basis for inclusion in management
plans and advocacy interventions for MMPL. Based on frequency records, these
species are not widely-adapted and their elevation range is limited. Alongside
that is the gradual increase of human-led activities that can potentially
threaten the health of the landscape. The rise of tourist sites, plantation
areas, and human settlements around MMPL, collection of wildlife species in
prohibited zones, and unauthorized trekking activities in MMPL would in the
long run cause degradation of the landscape. Moreover, majority of these
locally threatened flora are found along montane to upper montane forest
(1,600─2,000 m). As such, this study proposed for the recognition of this
altitudinal range as fern biodiversity hotspot. As such, conservation programs
can be focused towards the species in this zone as they could be the most
sensitive to environmental changes and may in the future vanish in the landscape.
CONCLUSION
The discovery of more than one
hundred new records for South Central Mindanao region and MMPL highlights its
rich natural heritage and confirms its significance as key biodiversity area
for pteridophytes. It is a significant addition to current botanical
information as it addressed gaps in knowledge of ferns and lycophytes. The determination of conservation priority
species and hotspot fern area (1,600─2,000 m) is hoped to serve as vital
reference for the integration of pteridophytes in local conservation plans for
MMPL.
Table 1. Composition of new
records in MMPL (with exsiccatae) and description of their spot characters and
habit.
|
Families and species
composition (Common Name) |
Description |
Habit |
Exsiccata |
|
I. Lycopodiopsida
(Fern Allies) |
|
|
|
|
1. Lycopodiaceae |
|
|
|
|
Huperzia javanica (Sw.) Fraser-Jenk. (Fir clubmosses) |
Stem ascending, dichotomously
branched, leaves whorled, narrowly elliptic, margin serrate, apex caudate,
spores trilete |
Epiphyte. |
OBEMIO453MSU |
|
Lycopodium clavatum L. (Common clubmoss) |
Stem creeping with erect tips,
dichotomously branched of unequal length, leaves small, moss-like, spirally
arranged, dimorphic strobili, adventitious roots present |
Ground. |
OBEMIO587MSU |
|
Phlegmariurus delbrueckii A.R. Field &
Bostock (Tassel fern) |
Pinnate, leaves alternate,
compact, ovate-obtuse, 3 mm wide x 5 mm long, apex rounded-cuspidate, base
cuneate, strobili dichotomous 20─35 mm, straight |
Epiphyte |
OBEMIO451MSU |
|
Phlegmariurus verticullatus (L.f) A.R. Field
(Tassel fern) |
Stems dichotomously branching,
leaves bristle-like, strobili terminal |
Epiphyte |
OBEMIO419MSU |
|
Pseudodiphasium volubile (G. Forst.) Holub |
Scrambling, horizontal stems,
spreading, numerous dichotomous branching, dimorphic, fertile stems with
short linear leaves, pendulous strobili at tip, sterile leaves widely spaced,
linear-peltate. |
Ground. |
OBEMIO555MSU |
|
2. Selaginellaceae |
|
|
|
|
Selaginella boninensis Baker (Spikemoss) |
Stems long, creeping, large
leaves oblong, alternate small leaves ovate, spiral, apex acute, base
rounded, rhizophore filiform |
Lithophyte |
OBEMIO485MSU |
|
Selaginella biformis A. Br. ex Kuhn (Spikemoss) |
Stems long, creeping, branched
on upper part, stramineous, primary leafy branches flattened, ovate, leaves
on stem ovate-lanceolate, apex acute, base rounded, rhizophore on rhizomes |
Lithophyte |
OBEMIO549MSU |
|
Selaginella engleri Hieron (Spikemoss) |
Stems erect, fronds bipinnate,
alternate, pinna ovate, sporangia at tips of fertile pinna, branched
microphylls contiguous |
Ground |
OBEMIO7396PBDH |
|
Selaginella gastrophylla Warb. (Spikemoss) |
Stems erect, fronds bipinnate,
alternate, pinna ovate, leaves on stems unappressed, widely spaced,
microphylls not contiguous, sporangia at tips of fertile pinna, cylindrical |
Ground |
OBEMIO488MSU |
|
Selaginella involvens (Sw.) Spring (Spikemoss) |
Stems erect, leaves on stems
scale-like, pale yellow, median stems branched, fronds pinnate,
ovate-triangular, ventral leaves contiguous, sporangia terminal |
Lithophyte |
OBEMIO486MSU |
|
Selaginella remotifolia Spring (Spikemoss) |
Stems branched from base; secondary
branches forked. Fronds pinnate, axillary leaves ovate, acute, leaves on
branches elliptic-lanceolate, not overlapping |
Ground |
OBEMIO489MSU |
|
II. Polypodiopsida
(Ferns) |
|
|
|
|
1. Aspleniaceae |
|
|
|
|
Asplenium affine Sw. |
Pinnatifid-bipinnatifid.alternate,
opposite at base, petiolulate, lobed, acuminate apex, pinnules aternate,
rounded apex, cuneate base, stalked, acroscopic pinnules smaller, lower
pinnules more lobed. Sori linear forming V shape over lamina veins |
Lithophyte |
OBEMIO052MSU |
|
Asplenium cuneatum Lam. |
Lamina ovate. Pinna triangular,
apex aristate, base convex, pinnules fan-shape, basal pinnules larger, lobed,
apex toothed, base convex-truncate, actinodromous. Sori linear 3─4
interspersed over veins |
Epiphyte |
OBEMIO053MSU |
|
Asplenium elmeri Christ |
Stipe clumped or solitary,
Lamina bipinnate, ovate, alternate, pinnules alternate, basal pinnule larger,
fan-shaped. Sori laminar, linear, single or paired at segments. |
Lithophyte |
OBEMIO056MSU |
|
Asplenium horridum Kaulf. (Lacy spleenwort) |
Stipe scaly, lamina pinnate,
alternate, lobes cut down halfway the costa, margin with deep
sinuses, pinna linear-lanceolate, apex attenuate, base convex. Sori
linear parallel and very near the costa |
Ground |
OBEMIO074MSU |
|
Asplenium laserpitiifolium Lam. |
Lamina tripinnate, alternate,
pinnae ovate, pinnules obovate, rachis dark brown, apex acute, base cuneate.
Sori linear incline over veinlets. |
Epiphyte |
OBEMIO7283PBDH |
|
Asplenium lobulatum Mett. |
Stipe clumped (2 or more),
Lamina pinnate, triangular, acuminate apex, truncate base, basiscopic pinna
opposite, acroscopic subopposite, reduced, pinnules lanceolate,
acuminate, truncate-cuneate-convex base, margin serrate. Some basal pinnules
forming prominent lobes on one side of the blade. Sori linear, inclined close
to midrib |
Epiphyte |
OBEMIO169MSU |
|
Asplenium longissimum Blume (Spleenwort) |
Pinnate, ovate, attenuate apex,
base, truncate, pinna alternate, stalked or sessile, apex attenuate, base
truncate-convex. Sori linear dark-brown inclined close to costa |
Ground |
OBEMIO7395PBDH |
|
Asplenium pellucidum Lam. |
Stipe clumped, Lamina elliptic,
pinna lanceolate-triangular, leaf base covering rachis on the ventral side,
margin lobed, apex acute, base truncate. Sori linear inclined with ends
touching the costa |
Epiphyte |
OBEMIO303MSU |
|
Hymenasplenium excisum (C. Presl) S.
Linds. |
Pinnate, thin, papyraceous,
wedge-shape, rounded apex, truncate base, toothed, unlobed, sori linear
over veinlets, 2 venation cladodromous, decurrent attachment, stele
haplostele, x-shape xylem. |
Epiphyte |
OBEMIO049MSU |
|
Hymenasplenium subnormale Copel. |
Pinnate, lamina
ovate-triangular, cordate base, attenuate apex, pinna ovate reduced at apex,
opposite-subopposite, rounded apex, truncate base., sori linear, inclined
halfway from costa |
Lithophyte |
OBEMIO7379PBDH |
|
2. Athyriaceae |
|
|
|
|
Athyrium puncticaule (Blume) T. Moore (Lady fern) |
Evergreen pinnatifid, Lamina
triangular-lanceolate, pinna stalked, margins serrate, apex acute, base
cuneate, basiscopic pinna strongly auriculate. Sori medial on the veins,
round |
Ground |
OBEMIO7252PBDH |
|
Athyrium nakanoi Makino (Lady fern) |
Evergreen, rhizome
creeping-ascending, erect, frond solitary or caespitose, bipinnate, lamina
papyraceous, pinnae linear-lanceolate,pinnules, pinnatifid, deltoid, apex
acuminate, base truncate, basal pinnules ovate-lanceolate.margin shallowly
lobed. Sori continuous, U-shape, over tertiary veins |
Ground |
OBEMIO7251PBDH |
|
Cornopteris banaohensis (C. Chr.) K.
Iwats. & M.G.Price |
Stipe clumped, frond
coriaceous, short, Lamina short, papyraceous, lower pinna bipinnatisect,
opposite, larger than acroscopic pinna. Pinna apex acuminate, pinnules
cuneate, base truncate, dissection almost to the midrib. Sori parallels the
midrib, bright orange |
Ground |
OBEMIO7253PBDH |
|
Diplazium dilatatum Blume (Twinsorus ferns) |
Fronds pinnate-bipinnatifid,
lamina dark green adaxially, pinna opposite-sub-opposite, sessile-subsessile,
acroscopic pinna smaller, less lobed, base of pinnule wider, apex acuminate,
base truncate. Sori linear inclined along costa forming v-shape |
Ground |
OBEMIO235MSU |
|
Diplazium geophilum Alderw. (Twinsorus ferns) |
Evergreen. pinnate, lamina
ovate, pinnae short-stalked, wide ovate, rounded-acute apex, base of the
pinna asymmetric, deeply-lobed. Sori linear grooved over craspedodromous
veinlets. |
Ground |
OBEMIO225MSU |
|
Diplazium sorzogonense (C. Presl.) C.
Presl. (Twinsorus ferns) |
Stipe clumped, fronds
pinnatifid, pinnae oblong-triangular, apex acuminate, base cuneate, basal and
apical segments reduced. Sori linear, on veinlets half-way to margin |
Ground |
OBEMIO602MSU |
|
3. Cyatheaceae |
|
|
|
|
Alsophila apoensis (Copel) R.M. Tryon (Tree fern) |
Tree fern. Tripinnatifid, Frond
glabrescent, coriaceous, pinnules sessile, oblong, short acuminate, segments
serrulate toward apex. Sori costal, globose |
Ground |
OBEMIO7255PBDH |
|
Alsophila hermannii R.M. Tryon (Tree fern) |
Tree fern. Tripinnatifid, Frond
glabrescent, coriaceous, pinnules sessile, triangular, caudate, truncate,
serrulate toward apex. Sori costal, globose |
Ground |
OBEMIO7256PBDH |
|
Alsophila heterochlamydea (Copel.) R.M.
Tryon (Tree fern) |
Tree fern. Tripinnatifid,
Pinnules sessile, pinnate at base, segments oblong, serrulate at apex. Sori
costal, obsolete. |
Ground |
OBEMIO016MSU |
|
Sphaeropteris elmeri (Copel) R.M. Tryon (Tree fern) |
Tree fern. Tripinnate. Pinnules
triangular, apex caudate, base truncate, segments, oblong, apex rounded,
thin, papyraceous. Sori costal, small, circular on sides of secondary veins |
Ground |
OBEMIO177MSU |
|
Sphaeropteris glauca (Blume) R.M. Tryon (Tree fern) |
Tree fern. Tripinnate. Pinnules
triangular, acuminate apex, truncate base, untoothed, segments oblong,
papyraceous, rounded apex, sessile, up to 14 veins on a side. Sori costal,
globose about 7 pairs |
Ground |
OBEMIO029MSU |
|
Sphaeropteris lepifera (J.Sm. ex Hook.)
Copel. (Tree fern) |
Tree ferns. Tripinnate,
Pinnules short-stalked, oblong, truncate base, segments pinnate, linear,
acute apex. Sori costal, globose |
Ground |
OBEMIO7257PBDH |
|
4. Dennstaedtiaceae |
|
|
|
|
Histiopteris incisa (Thunb.) J.Sm. (Bat’s wing fern) |
Rhizome robust, creeping,
fronds widely spaced, widely ovate slightly dimorphic with fertile lobes
slightly narrower, pinnae pale green, opposite, wide-angle with deep lobation
on margins, sori marginal continuous, linear and exindusiate surrounded
by reflexed leaf margin. |
Ground |
OBEMIO7258PBDH |
|
Miicrolepia strigosa (Thunb.) C. Presl (Lace Fern) |
Fronds wide-ovate,
bipinnatifid, pinnae alternate, attenuate apex, convex base, pinnules
subsessile, |
Ground |
OBEMIO7259PBDH |
|
Monachosorum henryi Christ |
Rhizome erect. Lamina
ovate-triangular, pinna oblong, pinnules ovate-lanceolate, base
truncate-round, thin, basal pinnules more lobed, apical pinnules more
lanceolate, sori circular at vein ends, petiole round, solenostele stele,
2-linear vascular bundles |
Ground. |
OBEMIO176MSU |
|
5. Dicksoniaceae |
|
|
|
|
Dicksonia amorosoana Lehnert &
Coritico (Amoroso’s wooly tree fern) |
Ground tree fern.
tripinnatifid, lamina dark green adaxially, light green abaxially, pinna
subsessile, lanceolate, base truncate, attentuate apex, basal segmentshorter,
sori circular, spores globose |
Ground. |
OBEMIO7260PBDH |
|
6. Dryopteridaceae |
|
|
|
|
Arachniodes amabilis (Blume)
Tindale |
Rhizome creeping, Fronds
oblong-ovate, bipinnate, coriaceous, acroscopic pinnules reduced, apex
caudate, base cuneate. Sori terminal on veinlets |
Ground, Lithophyte |
OBEMIO7325PBDH |
|
Bolbitis heteroclita (C. Presl) Ching |
Rhizome horizontal. Frond
odd-pinnate, opposite, apical lamina larger, elliptic, caudate apex, cuneate
base, margin crenose, dimorphic, secondary veins brochidodromous, tertiary
veins reticulate, opposite-subopposite, tertiary veins. Sori naked covering fertile
blades |
Epiphyte
|
OBEMIO7261PBDH |
|
Dryopteris hendersonii (Bedd.) C. Chr. (Wood fern). |
Tripinnatifid. Fronds wide
ovate, pinnae alternate, base pinnae larger, pinnules triangular-oblong,
acuminate apex, truncate-oblique base, lobe, apex toothed. Sori round,
indusiate |
Ground |
OBEMIO484MSU |
|
Dryopteris purpurascens (Blume) Christ (Wood fern). |
Frond
pinnatisect-bipinnatisect, alternate, pinnae triangular, apex acuminate with
alternate tooth along margins, pinnules triangular, acuminate apex, rounded
base, base pinnules of larger pinna pinnate, toothed, acroscopic pinnules
toothed. Sori costal, round, side by side the midvein. |
Ground |
OBEMIO502MSU |
|
Dryopteris permagna M. Price (Wood fern). |
Ground, bipinnatifid on
acroscopoc pinna tripinnatifid on lower pinna, alternate, triangular,
acuminate apex, base truncate, acroscopic segments pinnatisect, lower to
middle segments serrate. Sori round, parallel along midrib and secondary
veins |
Ground |
OBEMIO7262PBDH |
|
Polystichum moluccense T. Moore |
Tripinnate, alternate, dark
green adaxial, pinnae oblong, acuminate apex, rounded base, pinnules thick,
rough, ovate-triangular, base lobed, truncate-oblique, apex acute, toothed.
Sori round, laminar over veinlet tips |
Epiphyte |
OBEMIO393MSU |
|
Polystichum elmeri Copel. |
Bipinnate, alternate, light
green on adaxial, pinnae oblong, acuminate apex, convex base, pinnules thick,
rough, ovate, base truncate-oblique. |
Epiphyte |
OBEMIO5833MSU |
|
Teratophyllum aculeatum (Blume) Mett. ex
Kuhn |
Bathyphylls pinnate-bipinnate,
alternate, dichotomously branched, rhizome creeping. Lamina pinnate,
lanceolate. Fertile pinnae alternate, linear. Sori continuous covering entire
blade of fertile leaf. |
Epiphyte/ Climber |
OBEMIO7263PBDH |
|
7. Hymenophyllaceae |
|
|
|
|
Abrodictyum pluma (Hook.) Ebihara
& K. Iwats. |
Rhizome creeping. Fronds
tufted, alternate, oblong, opposite at base, pinna reduced, needle-like
middle pinna larger, segments clumped, dichotomous tips. Sori cup-shape at
vein ends of basal segments. |
Epiphyte |
OBEMIO468MSU |
|
Abdrodictyum obscurum (Blume) Ebihara
& K. Iwats. |
Rhizome creeping, stipe dark or
light brown, lamina tripinnate-quadripinnate, herbaceous, triangular-ovate,
pinnae oblong-ovate, apex obtuse-acute, widely-tooth, base cuneate. Sori
apical on some segments, involucres cylindrical. |
Lithophyte |
OBEMIO469MSU |
|
Crepidomanes minutum (Blume) K. Iwats. |
Rhizome branching, stipe dark
brown, lamina ovate, base cuneate, thin filmy, entire, segments linear, apex
obtuse, base rounded-cordate. Involucres funnelform |
Lithophyte |
OBEMIO7264PBDH |
|
Crepidomanes grande (Copel.) Ebihara
& K. Iwats. |
Rhizome short, erect, tufted
fronds, lamina quadipinnate, ovate-oblong, Sori tubular on distal part of
fronds |
Ground, Lithophyte |
OBEMIO735MSU |
|
Hymenophyllum ramosii Copel. (Filmy fern) |
Rhizomes long, creeping, lamina
pinnate-tripinnatifid, elliptic-triangular, alternate, pinna ovate, Sori
bud-shape on apical portion of lamina |
Epiphyte |
OBEMIO616MSU |
|
Hymenophyllum denticulatum Sw. (Filmy fern) |
Rhizomes long, creeping, rachis
narrowly-winged, toothed, lamina bipinnatifid, pinnae alternate, wide-ovate,
margins wide-serrate, veins prominent at abaxial portion. Sori cup-shape at
tips of acroscopic segments |
Epiphyte, Lithophyte |
OBEMIO546MSU |
|
Hymenophyllum fimbriatum J. Sm (Filmy fern) |
Rhizomes long, creeping, rachis
narrowly-winged entire nearly toward the base, alternate, elliptic, pinna
ovate pinnatisect, Sori at tip of acroscopic segments with slightly extruded
involucres |
Epiphyte, Lithophyte |
OBEMIO545MSU |
|
Hymenophyllum holochilum (Bosch) C. Chr.
(Filmy fern) |
Rhizome long, creeping, rachis
narrowly-winged almost inconspicuous, pinnatifid, alternate, margins toothed,
elliptic, pinnae deltoid, sparsely toothed, unequally cuneate-oblique. Sori
on acroscopic segments, involucres elongate-elliptic, receptacles exserted. |
Epiphyte, Lithophyte |
OBEMIO7266PBDH |
|
Hymenophyllum imbricatum Blume (Filmy fern) |
Rhizomes, long, creeping,
bipinnatifid, stipe and rachis winged, lamina bipinnatifid, alternate, wide
space between pinnae, pinnae wide-ovate, terminal segments filiform margin
entire, sori involucre wide, round. |
Epiphyte |
OBEMIO544MSU |
|
Hymenophyllum nitidulum (Bosch) Ebihara
& K. Iwats. (Filmy fern) |
Rhizomes long, creeping,
filiform, stipes almost wingless, lamina obovate, dichotomously lobed,
dissected at base, lobes linear or forked. Sori terminal on lobes, involucres
deltoid-like, sunken |
Epiphyte |
OBEMIO736MSU |
|
Hymenophyllum pallidum (Blume) Ebihara
& K. Iwats. (Filmy fern) |
Rhizomes long, creeping, stipes
hairy at base, lamina bipinnatifid, oblong, obtuse apex, cuneate base, pinnae
alternate, sessile, ovate. Sori terminal on acroscopic pinnae, enclosed |
Epiphyte, Lithophyte |
OBEMIO547MSU |
|
Hymenophyllum serrulatum (C. Presl) C. Chr.
(Filmy fern)
|
Rhizome, long, creeping, stipe
hairy, wingless, lamina translucent, ovate, bipinnatifid-tripinnatifid, pinna
alternate, oblong-ovate,stalked, apex round, lobed. Sori axillary on
acroscopic portion |
Epiphyte |
OBEMIO601MSU |
|
Hymenophyllum thiudium Harrington (Filmy fern) |
Rhizome, long, creeping, stipe
narrowly winged, lamina bipinnatifid-tripinnatifid, pinna alternate, ovate,
sori at terminal tips of ultimate segments, involucres capitate. |
Epiphyte |
OBEMIO7268PBDH |
|
Vandenboschia auriculata (Blume) Copel. |
Frond creeping, alternate,
oblong, petiolulate, basal pinnules wider, wide ovate. Sori apical on
acroscopic segments. |
Epiphyte |
OBEMIO7269PBDH |
|
8. Hypodematiaceae |
|
|
|
|
Leucostegia truncata (D. Don)
Fraser-Jenk. |
Fronds tripinnate, ovate,
coriaceous, pinna alternate, triangular, size increasing toward base,
pinnules ovate-triangular, apex acuminate, base convex, basal segments in
basal pinnae deeply lobed, widely ovate, rounded base, obtuse apex. Sori
kidney-shaped on veinlet ends. |
Ground |
OBEMIO347MSU |
|
9. Lindsaceae |
|
|
|
|
Odontosoria retusa (Cav.) J. Sm. |
Fronds tripinnate-pinnate,
pinnae alternate, ovate, stalked decurrent to rachis, acuminate apex, base
convex, pinnules fan-shape, stalked, truncate apex, cuneate base.Sori linear
on apex of pinnules in false indusium |
Ground |
OBEMIO737MSU |
|
Tapeinidium pinnatum (Cav.) C. Chr. |
Rhizome short, creeping, fronds
pinnate, elliptic-oblong, papyraceous, pinna linear, apex acuminate,
subsessile, rachis stramineous, margin shallowly crenate, apex acuminate,
base cuneate. Sori submarginal on vein ends, cup-shape indusia |
Ground |
OBEMIO7274PBDH |
|
Tapeinidium gracile (Blume) Alderw. |
Rhizome short, creeping, fronds
ovate, alternate, pinna elliptic-linear, acuminate apex, rounded base, upper
pinna pinnatifid, lower pinnules pinnatifid, linear. Sori round, marginal |
Ground |
OBEMIO738MSU |
|
Lindsaea pulchella (J. Sm.) Mett. ex
Kuhn |
Rhizome long, creeping, fronds
linear, acuminate apex, papyraceous, lower pinnae opposite, upper
sub-opposite, triangular, truncate apex, cuneate base. Sori submarginal on
vein ends. |
Epiphyte, Climber |
OBEMIO7270PBDH |
|
Osmolindsaea odorata (Roxb.) Lehtonen
& Lehtonen |
Rhizome short, creeping, fronds
pinnate, lamina wide, lanceolate, pinnae alternate, truncate apex, slightly
lobed convex base. Sori marginal, elongated, interrupted |
Lithophyte |
OBEMIO739MSU |
|
10. Marratiaceae |
|
|
|
|
Angiopteris evecta Sw. (Giant fern) |
Fronds tripinnate, alternate,
pinna elliptic-oblong, fleshy, pinnules stalked, apex acuminate, serrate,
rounded base, margin crenose, Sori submarginal, oval shape. |
Ground |
OBEMIO7275PBDH |
|
Ptisana pellucida (C. Presl) Murdock |
Fronds bipinnate, alternate,
fleshy, pinna ovate, pinnules lanceolate, apex acuminate, base rounded,
margins serrate. Sori oval, submarginal. |
Ground |
OBEMIO428MSU |
|
11. Oleandraceae |
|
|
|
|
Oleandra sibbaldi Grev. |
Rhizome long-creeping, fronds
elliptic, base cuneate, apex acuminate, membranous, with sparse catenate
hairs, costa, hairy, darker on lower surface. Sori inframedial, reniform. |
Epiphyte |
OBEMIO091MSU |
|
12. Ophioglossaceae |
|
|
|
|
Botrychium daucifolium Wall. ex Hook.
& Grev. (Moonwort) |
Rhizome erect, lamina
bipinnate, pinnate to bipinnate, herbaceous, pinnae alternate-subopposite,
short stalked or subsessile, triangular, pinnules ovate, apex
acute-acuminate, base rounded, serrate, basal pinnules lobed. Sori round on
separate fertile stalks |
Ground |
OBEMIO7276PBDH |
|
13. Plagiogyriaceae |
|
|
|
|
Plagiogyria glauca (Blume) Mett. |
Pinnate, Fronds ovate, pinna
linear, acuminate, base truncate, subsessile, glaucous ventral surface,
adaxial surface green, margin serrate. Sori tetrahedral |
Ground, Lithophyte |
OBEMIO473MSU |
|
14. Polypodiaceae |
|
|
|
|
Calymmodon gracillimus (Copel.) Nakai ex
H. Itô |
Small, caespitose, linear,
segments alternate, triangular, up to 2mm. Sori round numerous enclosed by
folds of margin. |
Epiphyte |
OBEMIO7277 PBDH |
|
Chrysogrammitis glandulosa (J.Sm.) Parris |
Pinnatisect. Lamina lanceolate,
apex acute, base cuneate. Segments triangular, larger at middle, decreasing
toward apex. Sori round, 1 in acroscopic segments, 2-3 along middle segments. |
Epiphyte |
OBEMIO033MSU |
|
Drynaria aglaomoprha Christenh (Oak leaf fern) |
Pinnatisect, dimorphic,
coriaceaous, margin crenose. Sori continuous, oval-square-shaped almost
filling the segment |
Epiphyte, Lithophyte |
OBEMIO7279 PBDH |
|
Drynaria descensa Copel. (Oak leaf fern) |
Pinnatisect, dimorphic,
coriaceous, margin crenose. Sori circular scattered on abaxial surface |
Epiphyte, Lithophyte |
OBEMIO7280PBDH |
|
Dasygrammitis malaccana (Baker) Parris (Shaggy fern) |
Stipe clumped, fronds pinnate,
lanceolate-oblong, aristate, base cuneate, pinna alternate-sub-opposite,
sessile, linear, apex rounded. Sori continuous on apical portion of pinna |
Epiphyte |
OBEMIO740MSU |
|
Goniophlebium subauriculatum (Blume) C. Presl
(Lacy Pine Fern) |
Pinnate, alternate, pinna
linear, light green, apex acuminate, base auriculate, short-stalked, margin
mildly serrate. Sori globose, parallel with midrib, within reticulate
veinlets |
Epiphyte |
OBEMIO467MSU
|
|
Goniophlebium persicifolium (Desv.) Bedd. |
Pinnate, alternate, stalked,
pinna lanceolate, apex narrowly acuminate, base oblique, margins crenose to
mildly serrate. Sori orbicular on both sides of midrib within reticulate
veinlets |
Epiphyte |
OBEMIO539MSU |
|
Goniophlebium pseudoconnatum Copel. |
Pinnate, alternate, pinna
linear, dark green, apex acuminate, base auriculate, short-stalked, margin
mildly serrate. Sori globose, parallel with midrib, within reticulate
veinlets. |
Epiphyte
|
OBEMIO540MSU |
|
Leptochilus insignis (Blume)
Fraser-Jenk. |
Pinnatisect. Pinna broadly
ovate, rounded base, acute apex, sinus increasing to the base, segments
elliptic, aristate. Sori oval randomly interspersed |
Epiphyte. |
OBEMIO115MSU |
|
Loxogramme avenia (Blume) C.
Presl |
Simple, lamina linear-obovate,
acute apex, base attenuate, midrib raised on abaxial side, symmetrical. Sori
tubular, parallel the midrib on acroscopic side. |
Epiphyte. |
OBEMIO741MSU |
|
Loxogramme paralella Copel. |
Simple lamina, obovate. dark
green abaxial, light green adaxial, Sori linear lining the veins spaced
increasingly to the middle of the blade. |
Epiphyte. |
OBEMIO742MSU |
|
Loxogramme scolopendriodes (Gaudich.)
C.V.Morton |
Simple lamina, lanceolate, Sori
linear inclined on the midrib at acroscopic side |
Epiphyte, Lithophyte |
OBEMIO035MSU |
|
Oreogrammitis jagoriana (Mett ex Kuhn)
Parris & Sundue |
Simple, leaf linear,
hirsute,apex obtuse, base attenuate, margin entire, Sori circular,
exindusiate, one on each side of costa. |
Epiphyte |
OBEMIO057MSU |
|
Oreogrammitis reindwarti (Blume) Parris |
Simple, small-leaf, apex
acuminate, base attenuate, margin crenate or non-crenate, hirsute. Sori
circular, exindusiate, one on each side of midrib. |
Epiphyte |
OBEMIO596MSU |
|
Prosaptia celebica (Blume) Tagawa
& K. Iwats. |
Stipe clumped, lamina elliptic,
pinnatisect, coriaceous, pinnae linear. Sori oval, submarginal |
Epiphyte |
OBEMIO743MSU |
|
Prosaptia multicaudata (Copel) Parris |
Stipe clumped, lamina widely
elliptic, pinnatisect, coriaceous, pinna linear, apex attenuate. Sori oval at
an angle toward the midrib, halfway from apex never reaching the base |
Epiphyte. |
OBEMIO370MSU |
|
Selliguea albidosquamata (Blume) Parris |
Odd-pinnate. Alternate,
Long-stalked. Pinna lanceolate, stalked, apex acumate, base cuneate,
symmetrical, margin entire, lined with bright white scales. Sori small, dot
shape between the midrib and margin |
Epiphyte |
OBEMIO7287PBDH |
|
Thylacopteris papillosa (Blume) Kunze ex
J.Sm. |
Pinnate-pinnatisect.
Lanceolate. Thin, papery. Pinna linear, round apex, lowest pinna pinnate,
sessile.Sori at tip of veinlets, appearing to be embedded on the adaxial
side. Tertiary veins cladodromous |
Epiphyte |
OBEMIO7288PBDH |
|
Tomophyllum macrum (Copel.) Parris |
Stipe clumped, pinnatisect,
subopposite, segments linear-elliptic, round apex, rachis and midrib
prominent, black, Sori round exindusiate, sub-marginal |
Epiphyte |
OBEMIO7289PBDH |
|
Tomophyllum millefolium (Blume) Parris |
Rhizome erect. Stipes in
whorls. Bipinnate-pinnatisect, Pinnules alternate, narrowly
linear. |
Epiphyte. |
OBEMIO7290PBDH |
|
15. Pteridaceae |
|
|
|
|
Adiantum hosei Baker (Maidenhair fern) |
Pinnate, trifoliate,
papyraceous, linear-lanceolate, pinnules alternate, sessile, oblong, stipe
thin, black, sori marginal, false indusium |
Ground. Lithophyte |
OBEMIO7291PBDH |
|
Antrophyum parvulum Blume |
Simple, thick, entire, obovate,
base attenuate, apex cuspidate-round. Sori linear over reticulate veins |
Ground |
OBEMIO577MSU |
|
Pteris oppositipinnata Fee (Brake fern) |
Ground. Broadleaved. pinnate,
Lamina thick, ovate, pinna opposite, pinnatisect, basal pinnae divergent,
ovate-oblong, acuminate apex, convex base, pinnules with rounded apex, sori
elongate, marginal, tertiary veins cladodromous |
Ground |
OBEMIO247MSU |
|
Vaginularia junghuhnii Mett. |
Rhizome short creeping, Stipe
clumped, pinna linear, coriaceous, apex acute, base cuneate. Sori continuous
at the abaxial side |
Epiphyte |
OBEMIO181MSU |
|
16. Tectariaceae |
|
|
|
|
Tectaria dissecta (G.Forst.)
Lellinger (Halberd fern) |
Rhizome ascending, Stipe
solitary, fronds pinnatifid-bipinnatifid, pinna subopposite, margin
deeply-lobed, apex acuminate, base obtuse, base segments pinnate, apex
rounded. Sori circular, marginal at acroscopic pinnae. |
Ground |
OBEMIO7298PBDH |
|
Tectaria melanocaulos (Blume) Copel. (Halberd fern) |
Stipe and rachis black,
innatifid-bipinnatifid large-leaf, wide-ovate, basal pinnae pinnate, margins
serrate and lobed, apex acuminate, base rounded. Sori interspersed over the
abaxial portion of the lamina |
Ground |
OBEMIO7297PBDH |
|
17. Thelypteridaceae |
|
|
|
|
Chingia ferox (Blume) Holttum |
Fronds pinnate, stipes to
rachis bristle-like, pinna alternate, short-stalked, acuminate, round base,
basal pinna oriented downwards, margin mildly lobed, Sori circular in
two adjacent rows within each lobe segment |
Ground |
OBEMIO7292PBDH |
|
Christella acuminata (Houtt.) Holttum |
Pinnatifid, lamina wide-ovate,
pinna opposite at base, sub-opposite towards acroscopic pinna, acuminate,
base sagittate with basal pinna oriented downwards, pinnae triangular,
acuminate, truncate. Sori circular submarginal terminating at ends of lobes |
Ground |
OBEMIO179MSU |
|
Christella dentata (Forssk.) Brownsey
& Jermy |
Pinnatifid, Lamina widely
elliptic, apical and basal pinna reduced, oblong, acuminate, basal pinna
oriented downwards, margins moderately lobed. Sori circular, submarginal |
Ground |
OBEMIO745MSU |
|
Pneumatopteris laevis (Mett.) Holttum |
Stipes clumped, frond pinnate,
widely-ovate, alternate, acuminate, pinnae lanceolate, |
Ground |
OBEMIO541MSU |
|
|
acuminate, obtuse. Sori
circular submarginal Stipes whorled, frond pinnate,
wide ovate, pinna linear-triangular, opposite-sub-opposite, lobed halfway to
costa. Sori circular at mid-portion of veinlets |
Ground |
OBEMIO7294PBDH |
|
Pronephrium nitidum Holttum |
Pinnatifid. Lamina wide ovate,
pinna opposite, deeply-lobed, 190 mm long x 130 mm wide, basal pinna pinnate
sessile, rachis black. Sori interspersed within tertiary veins forming
areoles. |
Lithophyte |
OBEMIO744MSU |
|
Sphaerostephanos ellipticus (Rosenst.) Holttum |
Stipes clumped, rachis pilose,
frond pinnate, wide-elliptic, pinna liner-triangular, acuminate, truncate,
margin moderately-lobed. Sori circular over lamina in lobe margins |
Ground |
OBEMIO7296PBDH |
Table 2. Economic uses from
several new records of ferns and lycophytes in MMPL.
|
Species |
Uses |
Reference |
|
Adiantum spp. |
Ornamental |
Oloyede 2012 |
|
Angiopteris evecta Sw. |
Medicinal. Leaf extract used to
treat dysentery, blood diseases and ulcers. Spores used to treat leprosy and
other skin diseases. Antiviral, antihyperglycemic and analgesic |
Benjamin 2011 |
|
Asplenium cuneatum Lam. |
Medicinal. Vermifuges
(anthelmintic) |
Burkill 1985 |
|
Asplenium spp. |
Ornamental |
Simpson 2019 |
|
Christella dentata (Forssk.) Brownsey
& Jermy |
Medicinal. Anti-bacterial.
Antihyperglycemic and analgesic activity of leaves |
Srivastava 2007; Manhas et al.
2018 |
|
Drynaria spp. |
Ornamental |
Simpson 2019 |
|
Dryopteris spp. |
Medicinal. Abortifacient,
anthelmintic. Food. Rhizomes source of fats (90% monoethenoid acids) |
May 1978; Srivastava 2007;
Mannan et al. 2008; |
|
Lycopodium clavatum L. |
Medicinal. Emetic for stomach
disorders, cure for kidney and lung diseases, analgesic, antioxidant,
anti-cancerm anti-inflammatory, neuroprotective, immunomodulatory and
hepatoprotectivel nosebleeding and heal wounds , treatment for learning and
memory impairment ,diuretic and anti-spasmatic , cure headaches . Household
Material (mats) |
May 1978; Srivastara 2007;
Benjamin 2011; Oloyede 2012;; Hanif et al. 2015; Bhardwaj & Misra 2018 |
|
Pseudodiphasium volubile (G. Forst.) Holub |
Ornamental. Table decoration |
Benjamin 2011 |
|
Odontosoria chinensis (L.) J. Sm. |
Medicinal. Cure for chronic
enteritis. Ornamental. landscape plant |
Ho et al. 2010; Oloyede 2012 |
|
Tree ferns (Alsophila,
Sphaeropteris) |
Food. Rhizomes as source of
starch |
Ripperton 1924; Leach 2003 |
Table 3. New records in MMPL
highlighting their category as to geographic distribution, international
(IUCN), national (DAO) and local assessment based on relative frequency (RF).
|
Families and Species
Composition |
Species category as regards
geographic distribution |
IUCN |
DAO 2017-11 |
Relative Frequency (RF) |
Local Assessment based on RF |
|
2021 |
|
||||
|
1. Lycopodiaceae |
|
|
|
|
|
|
Huperzia javanica (Sw.) Fraser-Jenk. |
Indigenous |
NA |
OWS |
0.403 |
VU |
|
Lycopodium clavatum L. |
Indigenous |
NA |
OWS |
0.109 |
EN |
|
Phlegmariurus delbrueckii A.R. Field &
Bostock |
Indigenous |
NA |
OWS |
0 |
CR |
|
Phlegmariurus verticullatus (L.f) A.R. Field |
Indigenous |
NA |
OWS |
0.019 |
CR |
|
Pseudodiphasium volubile (G. Forst.) Holub |
Indigenous |
NA |
OWS |
0 |
CR |
|
2. Selaginellaceae |
|
|
|
|
|
|
Selaginella boninensis Baker |
Indigenous |
NA |
OWS |
0.33 |
EN |
|
Selaginella biformis A. Br. ex Kuhn |
Indigenous |
NA |
OWS |
0.11 |
EN |
|
Selaginella cupressina (Willd.) Spring |
Indigenous |
NA |
OWS |
0.11 |
EN |
|
Selaginella engleri Hieron. |
Indigenous |
NA |
OWS |
0.22 |
EN |
|
Selaginella gastrophylla Warb. |
Indigenous |
NA |
OWS |
0.7 |
NT |
|
Selaginella involvens (Sw.) Spring |
Indigenous |
NA |
OWS |
0.44 |
VU |
|
Selaginella remotifolia Spring |
Indigenous |
NA |
OWS |
0.28 |
EN |
|
1. Aspleniaceae |
|
|
|
|
|
|
Asplenium affine Sw. |
Indigenous |
NA |
OWS |
0 |
CR |
|
Asplenium cuneatum Lam. |
Indigenous |
NA |
OWS |
0.14 |
EN |
|
Asplenium elmeri Christ |
Indigenous |
NA |
OWS |
0.31 |
EN |
|
Asplenium horridum Kaulf. Asplenium laserpitiifolium Lam. |
Indigenous Indigenous |
NA NA |
OWS OWS |
0.31 0.21 |
EN EN |
|
Asplenium lobulatum Mett. |
Indigenous |
NA |
OWS |
1.56 |
LC |
|
Asplenium longgisimum Blume |
Indigenous |
NA |
OWS |
0.7 |
NT |
|
Asplenium pellucidum Lam. |
Indigenous |
NA |
OWS |
0.44 |
VU |
|
Hymenasplenium excisum (C. Presl) S.
Linds. |
Indigenous |
NA |
OWS |
2.19 |
LC |
|
Hymenasplenium subnormale (Copel.) Nakaike |
Indigenous |
NA |
OWS |
0.22 |
EN |
|
2. Athyriaceae |
|
|
|
|
|
|
Athyrium nakanoi Makino |
Indigenous |
NA |
EN |
0.33 |
EN |
|
Athyrium puncticaule (Blume) T. Moore |
Indigenous |
NA |
OWS |
0.22 |
EN |
|
Cornopteris banaohensis (C. Chr.) K.
Iwats. & M.G. Price |
Indigenous |
NA |
OWS |
0 |
CR |
|
Diplazium dilatatum Blume |
Indigenous |
NA |
OWS |
1.44 |
LC |
|
Diplazium geophilum Alderw. |
Indigenous |
NA |
OWS |
0.38 |
EN |
|
Diplazium pseudocyatheifolium Rosenst. |
Indigenous |
NA |
EN |
0.22 |
EN |
|
3. Cyatheaceae |
|
|
|
|
|
|
Alsophila apoensis (Copel.) R.M.
Tryon |
Endemic |
NA |
EN |
0.42 |
VU |
|
Alsophila hermannii R.M. Tryon Sphaeropteris elmeri (Copel.) R.M.
Tryon |
Endemic Endemic |
NA NA |
EN VU |
1.56 0.28 |
LC EN |
|
Sphaeropteris glauca (Blume) R.M. Tryon |
Indigenous |
LC |
EN |
1.69 |
LC |
|
Alsophila heterochlamydea (Copel.) R.M.
Tryon |
Endemic |
NA |
VU |
1.56 |
LC |
|
Sphaeropteris lepifera (J.Sm. ex Hook.) R.M. Tryon |
Indigenous |
NA |
EN |
0.28 |
EN |
|
4. Dennstaedtiaceae |
|
|
|
|
|
|
Histiopteris incisa (Thunb.) J.Sm. |
Indigenous |
NA |
OWS |
0.88 |
NT |
|
Microlepia enulose (Thunb.) C. Presl |
Indigenous |
NA |
OWS |
0.22 |
EN |
|
Monachosorum henryi Christ |
Indigenous |
NA |
OWS |
2 |
LC |
|
5. Dicksoniaceae |
|
|
|
|
|
|
Dicksonia amorosoana Lehnert &
Coritico |
Endemic |
NA |
OWS |
0.42 |
VU |
|
6. Dryopteridaceae |
|
|
|
|
|
|
Bolbitis enulosete (C. Presl) Ching |
Indigenous |
NA |
OWS |
0.42 |
VU |
|
Dryopteris hendersonii (Bedd.) C. Chr. |
Indigenous |
NA |
OWS |
0.22 |
EN |
|
Dryopteris purpurascens (Blume) Christ |
Indigenous |
NA |
OWS |
0 |
CR |
|
Dryopteris permagna M. Price |
Indigenous |
NA |
EN |
0 |
CR |
|
Polystichum moluccense T. Moore |
Indigenous |
NA |
EN |
0.82 |
NT |
|
Polystichum elmeri Copel. |
Endemic |
NA |
OWS |
0.18 |
EN |
|
Teratophyllum aculeatum (Blume) Mett. ex
Kuhn |
Indigenous |
NA |
OWS |
0 |
CR |
|
7. Hymenophyllaceae |
|
|
|
|
|
|
Abrodictyum pluma (Hook.) Ebihara
& K.Iwats. |
Indigenous |
NA |
OWS |
0.56 |
VU |
|
Abdrodictyum obscurum (Blume) Ebihara
& K. Iwats. |
Indigenous |
NA |
OWS |
0.31 |
EN |
|
Crepidomanes minutum (Blume) K. Iwats. |
Indigenous |
NA |
OWS |
0 |
CR |
|
Crepidomanes grande (Copel.) Ebihara
& K. Iwats. |
Indigenous |
NA |
OWS |
0.14 |
EN |
|
Hymenophyllum ramosii Copel. |
Indigenous |
NA |
OWS |
0 |
CR |
|
Hymenophyllum denticulatum Sw. |
Indigenous |
NA |
OWS |
0.11 |
EN |
|
Hymenophyllum fimbriatum J. Sm. |
Indigenous |
NA |
OWS |
0.94 |
NT |
|
Hymenophyllum holochilum (Bosch) C. Chr. |
Indigenous |
NA |
OWS |
0 |
CR |
|
Hymenophyllum imbricatum Blume |
Indigenous |
NA |
OWS |
0.88 |
NT |
|
Hymenophyllum nitidulum (Bosch) Ebihara
& K. Iwats. |
Indigenous |
NA |
OWS |
0.14 |
EN |
|
Hymenophyllum pallidum (Blume) Ebihara
& K. Iwats. |
Indigenous |
NA |
OWS |
0.94 |
NT |
|
Hymenophyllum serrulatum (C. Presl) C. Chr. |
Indigenous |
NA |
OWS |
0.19 |
EN |
|
Hymenophyllum thiudium Harrington |
Indigenous |
NA |
OWS |
0.12 |
EN |
|
Vandenboschia auriculata (Blume) Copel. |
Indigenous |
NA |
OWS |
0.11 |
EN |
|
8. Hypodematiaceae |
|
|
|
|
|
|
Leucostegia truncata (D. Don)
Fraser-Jenk. |
Indigenous |
NA |
OWS |
0.88 |
NT |
|
9. Lindsaceae |
|
|
|
|
|
|
Lindsaea pulchella (J. Sm.) Mett. ex
Kuhn |
Indigenous |
NA |
OWS |
0.14 |
EN |
|
Odontosoria retusa (Cav.) J. Sm. |
Indigenous |
NA |
OWS |
0.14 |
EN |
|
Osmolindsaee odorata (Roxb.) Lehtonen
& Lehtonen |
Indigenous |
NA |
OWS |
0.14 |
EN |
|
Tapeinidium gracile (Blume) Alderw. |
Indigenous |
NA |
OWS |
0.14 |
EN |
|
Tapeinidium pinnatum (Cav.) C. Chr. |
Indigenous |
NA |
OWS |
0.28 |
EN |
|
10. Mariatiaceae |
|
|
|
|
|
|
Angiopteris evecta Sw. |
Indigenous |
NA |
OTS |
1.56 |
LC |
|
Ptisana pellucida (C. Presl) Murdock |
Indigenous |
NA |
OWS |
1.31 |
LC |
|
11. Oleandraceae |
|
|
|
|
|
|
Oleandra sibbaldi Grev. |
Indigenous |
NA |
OWS |
0.14 |
EN |
|
12. Ophioglossaceae |
|
|
|
|
|
|
Botrychium daucifolium Wall. ex Hook.
& Grev. |
Indigenous |
NA |
OWS |
0.75 |
NT |
|
13. Plagiogyriaceae |
|
|
|
|
|
|
Plagiogyria glauca (Blume) Mett. |
Indigenous |
NA |
OWS |
1.38 |
LC |
|
14. Polypodiaceae |
|
|
|
|
|
|
Calymmodon gracillimus (Copel.) Nakai ex
H. Itô |
Indigenous |
NA |
OWS |
0.13 |
EN |
|
Chrysogrammitis glandulosa (J.Sm.) Parris |
Indigenous |
NA |
OWS |
0.14 |
EN |
|
Dasygrammitis malaccana (Baker) Parris |
Indigenous |
NA |
OWS |
0.44 |
VU |
|
Drynaria aglaomorpha Christenh. |
Indigenous |
NA |
VU |
0.22 |
EN |
|
Drynaria descensa Copel. |
Endemic |
NA |
OWS |
0.11 |
EN |
|
Goniophlebium persicifolium (Desv.) Bedd. |
Indigenous |
NA |
OWS |
1 |
NT |
|
Goniophlebium pseudoconnatum (Copel.) Copel. |
Indigenous |
NA |
OWS |
1.44 |
LC |
|
Goniophlebium subauriculatum (Blume) C. Presl |
Indigenous |
NA |
OWS |
0 |
CR |
|
Leptochilus insignis (Blume)
Fraser-Jenk. |
Indigenous |
NA |
OWS |
0 |
CR |
|
Loxogramme avenia (Blume) C. Presl |
Indigenous |
NA |
OWS |
0.06 |
CR |
|
Loxogramme paralella Copel. |
Indigenous |
NA |
OWS |
0.06 |
CR |
|
Loxogramme scolopendriodes (Gaudich.)
C.V.Morton |
Indigenous Indigenous |
NA NA |
OWS OWS |
0 0.15 |
CR CR |
|
Oregrammitis beddomeana (Alderw) T.C. Hsu Oreogrammitis jagoriana (Mett. ex Kuhn)
Parris & Sundue |
Indigenous Indigenous |
NA NA |
OWS OWS |
0.19 0.15 |
EN CR |
|
Oreogrammitis reinwardtii (Blume) Parris |
Indigenous |
NA |
OWS |
0.14 |
EN |
|
Oreogrammitis torricelliana (Brause) Parris |
Indigenous |
NA |
OWS |
0.11 |
EN |
|
Prosaptia contigua (G. Forst.) C.
Presl Prosaptia celebica (Blume) Tagawa
& K. Iwats. |
Indigenous Indigenous |
NA NA |
OWS OWS |
0.14 0.15 |
EN CR |
|
Prosaptia multicaudatum (Blume) Tagawa
& K. Iwats. |
Indigenous |
NA |
OWS |
0 |
CR |
|
Prosaptia venulosa (Blume) M.G. Price |
Indigenous |
NA |
OWS |
0.14 |
EN |
|
Selliguea albidosquamata (Blume) Parris |
Indigenous |
NA |
OWS |
0.14 |
EN |
|
Thylacopteris papillosa (Blume) Kunze ex
J.Sm. |
Indigenous |
NA |
OWS |
0.33 |
EN |
|
Tomophyllum macrum (Copel.) Parris |
Endemic |
NA |
OWS |
0.14 |
EN |
|
Tomophyllum millefolium (Blume) Parris |
Indigenous |
NA |
OWS |
0.14 |
EN |
|
15. Pteridaceae |
|
|
|
|
|
|
Adiantum hosei Baker |
Indigenous |
NA |
OWS |
0.75 |
NT |
|
Antrophyum parvulum Blume |
Indigenous |
NA |
OWS |
0.14 |
EN |
|
Pteris oppositipinnata Fee |
Indigenous |
NA |
OWS |
1.25 |
LC |
|
Vaginularia junghunii Fee |
Indigenous |
NA |
OWS |
0.22 |
EN |
|
16. Thelypteridaceae |
|
|
|
|
|
|
Chingia ferox (Blume) Holttum |
Indigenous |
NA |
OWS |
0 |
CR |
|
Christella acuminata (Houtt.) Holttum |
Indigenous |
NA |
OWS |
0.89 |
NT |
|
Christella dentata (Forssk.)
Brownsey & Jermy |
Indigenous |
NA |
OWS |
0.11 |
EN |
|
Pneumatopteris laevis (Mett.) Holttum |
Indigenous |
NA |
OWS |
0.75 |
NT |
|
Pneumatopteris nitidula (C. Presl) Holttum |
Endemic |
NA |
OWS |
0 |
CR |
|
Pronephrium nitidum Holttum |
Indigenous |
NA |
OWS |
0 |
CR |
|
Sphaerostephanos ellipticus (Rosenst.) Holttum |
Endemic |
NA |
OWS |
0 |
CR |
|
17. Tectariaceae |
|
|
|
|
|
|
Tectaria melanocaulos (Blume) Copel. |
Indigenous |
NA |
OWS |
0 |
CR |
|
Tectaria dissecta (G. Forst.)
Lellinger
|
Indigenous |
NA |
OWS |
0 |
CR
|
For figure &
images - - click here for full PDF
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