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This study was conducted to assess the floral composition of the Alno communal mixed forest in the Philippines. A quadrat method of vegetational analysis was used for the assessment of trees, shrubs, saplings, and seedlings. A total of 78 species belonging to 43 families were identified in this communal forest. For the assessment of grasses, herbs, ferns, and other low-lying vegetation, the line intercept method was used. A total of 31 species belonging to 20 families were found using this method. The diversity (Shannon–Wiener) indices of this communal forest are 3.2129 and 2.3870 for the quadrat method and line intercept method, respectively. The most dominant species in this area is Pinus kesiya Royle ex Gordon (Benguet pine) with an importance value of 64.19 %. Endemic species in the area also connote ecological importance, being considered a good indication of the status of habitats and ecosystems of this communal forest.
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1 23
Landscape and Ecological
Engineering
ISSN 1860-1871
Volume 10
Number 2
Landscape Ecol Eng (2014) 10:361-368
DOI 10.1007/s11355-012-0204-5
Floral diversity assessment in Alno
communal mixed forest in Benguet,
Philippines
Roscinto Ian C.Lumbres, Jennifer
A.Palaganas, Sheryll C.Micosa, Kenneth
A.Laruan, Elvira D.Besic, Chung-Weon
Yun, et al.
1 23
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REPORT
Floral diversity assessment in Alno communal mixed forest
in Benguet, Philippines
Roscinto Ian C. Lumbres Jennifer A. Palaganas
Sheryll C. Micosa Kenneth A. Laruan
Elvira D. Besic Chung-Weon Yun Young-Jin Lee
Received: 13 October 2011 / Revised: 13 September 2012 / Accepted: 9 October 2012 / Published online: 2 November 2012
ÓInternational Consortium of Landscape and Ecological Engineering and Springer Japan 2012
Abstract This study was conducted to assess the floral
composition of the Alno communal mixed forest in the
Philippines. A quadrat method of vegetational analysis was
used for the assessment of trees, shrubs, saplings, and
seedlings. A total of 78 species belonging to 43 families
were identified in this communal forest. For the assessment
of grasses, herbs, ferns, and other low-lying vegetation, the
line intercept method was used. A total of 31 species
belonging to 20 families were found using this method. The
diversity (Shannon–Wiener) indices of this communal
forest are 3.2129 and 2.3870 for the quadrat method and
line intercept method, respectively. The most dominant
species in this area is Pinus kesiya Royle ex Gordon
(Benguet pine) with an importance value of 64.19 %.
Endemic species in the area also connote ecological
importance, being considered a good indication of the
status of habitats and ecosystems of this communal forest.
Keywords Biodiversity Vegetational analysis
Diversity index Pinus kesiya
Introduction
The Forest Management Bureau (FMB) of the Philippines
reported in 2003 that the Benguet Province of the Cordil-
lera Administrative Region (CAR) has a total of 8634 ha of
mixed forest (FMB 2003). Furthermore, forests that can be
found in this province are dominated by Pinus kesiya,
being classified as tropical lower montane rainforest
(Fernando et al. 2008). It is also reported that other Pinus
kesiya forest developed after human disturbance such as
burning for cultivation of broadleaved montane forest
(Fernando et al. 2008).
According to the Department of Environment and Nat-
ural Resources–United Nations Environment Programme
(DENR-UNEP), the Philippines has 15 biogeographic
regions, one of which is the CAR where the Alno forest is
located, due to the richness in the biological resources,
most especially the flora (DENR-UNEP 1997). Oyama
et al. (2003) reported that tropical rainforests such as those
in the Philippines have high richness of plant species. It has
also been characterized that, in tropical places, species
distribution varies from one location to another because of
biogeography, disturbance, and habitat (Whitmore 1984).
These biological resources also provide many different
goods and services not only to other organisms but most
especially to humans (Nakashizuka 2004). However, the
diversity of this region’s resources seems not to be given
enough attention, and extinction of important species has
been going on unnoticed. In Asia, the rate of biodiversity
loss is higher and becoming serious (Nakashizuka 2004),
including in the Philippines, due to environmental
destruction (PCSD-IEMSDP 1998). Excessive logging,
clearing and burning, shifting cultivation, environmental
pollution, and expansion of agricultural areas and human
settlements are among the reasons for environmental
R. I. C. Lumbres C.-W. Yun Y.-J. Lee (&)
Department of Forest Resources,
Kongju National University, Yesan,
Chungnam 340-802, South Korea
e-mail: leeyj@kongju.ac.kr
R. I. C. Lumbres J. A. Palaganas S. C. Micosa
K. A. Laruan E. D. Besic
College of Forestry, Benguet State University,
2601 La Trinidad, Benguet, Philippines
123
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DOI 10.1007/s11355-012-0204-5
Author's personal copy
destruction resulting in biodiversity loss. Thus, there is a
dire need to address the growing and nonstop degradation
of the environment to prevent biodiversity loss. Prance
et al. (2000) reported that large areas of tropical flora are
still understudied and information is still insufficient. The
basic premise for protection, preservation, and manage-
ment of these biological resources and to prevent the
soaring loss of biodiversity is to perform an inventory of
flora that still exists. According to Phillips et al. (2003), it
is necessary to conduct a floristic inventory to determine
the species diversity and understand the species distribu-
tion. Killeen et al. (1998) reported that floristic inventories
at specific localities are a rapid and effective method to
obtain significant information such as the identification of
rare, native, or endemic species, which is significant for
conservation plans and programs. Moreover, this inventory
will serve as a basis for policy formulation concerning the
areas which focus on preservation and protection of forests
(Bacudo et al. 2006). Their status regarding scarcity,
abundance, and utilization must be known in concomitance
with the identification of their location through mapping.
Application of geographic information system (GIS) is a
very important tool for protecting and managing the bio-
diversity of an area. Locations of threatened species can be
easily mapped using this system, providing an effective
tool for forest managers. Hence, the main objectives of this
study are to assess the existing floral diversity and develop
a spatial map and database for Alno communal forest in the
Philippines.
Materials and methods
Study site
The study site is located in the communal forest of Alno
Village in the municipality of La Trinidad, Benguet
Province, the Philippines (Fig. 1). It is accessible through
the Camp Dangwa–Alapang–Alno provincial road. Based
on the DENR cadastral survey, this village has an esti-
mated land area of 958.35 ha. It is the third largest village
in this municipality. The existing land uses of Alno are
agricultural lands with 318.56 ha (33.24 %), water
resources with 37.76 ha (3.94 %), residential land with
18.98 ha (1.98 %), roads with 56.64 ha (5.91 %), and
forest and brushlands with 526.42 ha (54.93 %). An area of
30.8 ha of forest and brushlands is classified as the Alno
communal forest. Alno is hilly to mountainous with slopes
ranging from 19 to 30 %, followed by upland areas with
slopes of 9–18 %, and rough mountainous areas with
slopes of 31–50 %.
Alno has average maximum and minimum temperature
of 24 and 15.1 °C, whereas the mean annual temperature is
19.6 °C based on 1971–2001 data. This area has two pro-
nounced seasons, dry from November to April and rainy
during the rest of the year, based on the Coronas System of
Classification (Lantican 2001). This area has annual pre-
cipitation of 3879 mm, while the mean annual relative
humidity is 86 %. Two types of soil exist in the area,
namely Puguis gravelly loam and Bineng loam. Puguis
Fig. 1 Location map of the study site in La Trinidad, Benguet, Philippines
362 Landscape Ecol Eng (2014) 10:361–368
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gravelly loam has good to excessive drainage. Bineng loam
soil has excessive external drainage and fair internal
drainage; this soil type is susceptible to soil erosion
(La Trinidad Municipality Official website 2011).
Alno communal forest is a secondary forest. Though the
study site was not subjected to commercial logging, it
served as a source of raw materials for various forest
products needed by members of the Alno community such
as fuel wood, construction materials, pasture land, and even
as a hunting ground during its primeval stage.
Data collection
Qualitative and quantitative approaches were performed in
this study. The qualitative approach covered the identifi-
cation of flora present in the area, while the quantitative
part made use of vegetational analyses using mathematical
formulae for biodiversity indices, density, frequency, and
height (PCARRD 1987). A total of six 50 m 950 m
quadrats were established in the Alno communal forest. All
trees, shrubs, saplings, and seedlings that fell within the
established quadrats were identified, counted, and mea-
sured. Likewise, grasses, herbs, and ferns were assessed
using the line intercept method. This was done by the
establishment of a 50-m transect line in each established
quadrat, and a total of six 5-m vertical lines at an interval
of 10 m were also established in each quadrat (PCARRD
1987). Grasses, herbs, and ferns that touched the vertical
lines were identified and counted. Figure 2shows the
layout of the quadrat and the transect line established for
the floral diversity assessment of Alno communal forest.
The information gathered in the field included the common
name, diameter at breast height (DBH, cm), and total
height (m) of each individual tree. DBH was measured at
1.3 m from the ground using a diameter tape while the total
height of trees was measured from the surface of the
ground to the tip of the tree using an Abney hand level.
Specific locations of all trees were identified using a
global positioning system (GPS) receiver (GPS V; Garmin,
USA). Using ArcView 3.2 GIS software, maps were cre-
ated showing the location of the trees found in the plots in
Alno.
Data analysis
Indices on the vegetation structure were computed using
the following formulae:
Density ðD;trees=m2Þ¼No. of plants of a certain species
Total area sampled 100;
ð1Þ
Relative density ðRDÞ¼ Density of a species
Total density for all species 100;
ð2Þ
Frequency ðFÞ¼Number of plots in which a species occurs
Total number of plots sampled ;
ð3Þ
Relative frequency ðRFÞ¼Frequency value for a species
Total frequency of all species 100;
ð4Þ
Relative height ðRHÞ
¼Summed height of all individuals for a species
Summed height of all individuals for all species 100;
ð5Þ
Importance value ðIVÞ¼RD þRF þRH:ð6Þ
Diversity indices were also determined using the
Shannon–Wiener index (Ito et al. 2006; Kodani 2006;
Nagai and Yoshida Nagai 2006; Wen et al. 2010)
computed as
H0¼Xpiln pi;ð7Þ
where H0is the diversity index, p
i
is the proportion of
individual species i, and ln is natural logarithm.
This information will provide a better quantitative
description of this forest regarding species importance and
function in its habitat compared with the density alone. The
rank or order for a particular species within the forest
community can be determined and quantified using this
Legend:
50m x 50m quadrat
50m transect line
5m vertical lines with
an interval of 10m
Fig. 2 Layout of the quadrat, transect line, and vertical lines for floral
diversity assessment in La Trinidad, Benguet, Philippines
Landscape Ecol Eng (2014) 10:361–368 363
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analysis (Kent and Coker 1992; Mueller-Dombois and
Ellenberg 1974).
Results and discussion
Floral assessment
Using the quadrat method, 78 tree species belonging to 43
families were identified in Alno Communal Forest. Mora-
ceae had the highest number of species of these families,
with 8 species. This was followed by Lamiaceae with six
species. Caprifoliaceae, Phyllanthaceae, and Rubiaceae
were the other families with higher numbers of species in
this communal forest, having four species each. On the
other hand, Pinaceae was the family with the highest
importance value of 64.19 %. The next most dominant
family was Moraceae with 30.18 %. Betulaceae, Melas-
tomataceae, and Juglandaceae were the other families that
dominated the area, with 24.12, 18.23, and 16.04 %
importance value, respectively.
On the species level, Pinus kesiya was the most domi-
nant species with an importance value of 64.19 % and
having 551 individual species. This species was found in
all quadrats and had the highest number of individuals in
five plots (Table 1). It was followed by Alnus japonica,
with importance value of 24.12 %. This species had 158
individuals that were found in four quadrats. Other species
with higher importance value were Engelhardtia spicata
var. colebrookeana with 14.48 %, Melastoma malabathri-
cum with 14.31 %, and Ficus annulata with 12 %
(Table 2).
The calculated diversity index in Alno communal forest
employing the quadrat method for overstory vegetation
analysis was 3.2129. On the other hand, a total of 31
species belonging to 20 families were identified by the line
intercept method (for grasses, herbs, and ferns), and the
calculated diversity index of species using this method was
2.3870 (Table 3).
An example of species with ecological function is the
Ficus spp. (tropical figs), which appeared to be one of the
abundant families present in this forest. This species can be
designated as both an umbrella species and keystone spe-
cies (Catinbog-Sinha and Heaney 2006) because it provides
food to a wide variety of and numerous fruit-eating birds,
wild pigs, and native rodents, among others. Aside from
this, Ficus nota and Cyathea contaminans are usually
associated with abundance of water or moisture in an area
(Bacudo et al. 2006).
Species with threatened condition were found in this
forest. The species Guioa reticulata was found to be crit-
ically endangered based on the DENR national list of
threatened Philippine plants (DENR 2007) (Table 2).
Saplings and seedlings of this species were encountered
specifically in quadrat 1, which was established on the
eastern part of the forest. The other two species categorized
in the vulnerable list were Cyathea contaminans and
Saurauia bontocensis. For the understory vegetation,
Anamirta cocculus and Hyptis suaveolens are categorized
as vulnerable, while Rubus fraxinifolius is categorized as a
threatened species (Table 3). Because of the presence of
threatened species in the area, there is a need to conserve
and protect this communal forest to prevent extinction of
these species.
The study of Gascon (1998) reported that the total
diversity (Shannon–Wiener index) of Hanunuo Mangyan
Agroforestry Systems in Sitio Dangkalan, Bulalacao,
Oriental Mindoro, Philippines is 1.2990 and Antidesma
bunius (Bignai) has the highest importance value of
27.9 %. Gevan
˜a and Pampolina (2009) reported that the
Table 1 General floristic information of the six plots established in Alno communal forest
Plot Quadrat method Line intercept method
Number
of
species
Number
of
families
Total number of trees,
shrubs, saplings, and
seedlings
Species with highest
number of individuals
(count)
Number
of
species
Number
of
families
Total number of
grasses, herbs,
and ferns
Species with highest
number of individuals
(count)
12317357 Pinus kesiya (76) 12 9 98 Miscanthus sinensis
(24)
22015400 Pinus kesiya (168) 13 9 258 Eupatorium sp. (131)
33222357 Alnus japonica (93) 14 8 251 Ageratina
adenophora (83)
43623639 Pinus kesiya (129) 18 12 293 Eupatorium sp. (105)
53425330 Pinus kesiya (59) 15 9 299 Eupatorium sp. (74)
63119470 Pinus kesiya (101) 17 9 484 Paspalum
conjugatum (223)
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Table 2 Overstory vegetation analysis and importance value of species present in Alno communal forest using quadrat method
Scientific name Family name Local name RD RH RF IV Status/endemism
Acer laurinum Aceraceae Philippine maple 0.16 0.16 0.58 0.89 Relatively rare/
indigenous
Agave sisalana Agavaceae Sisal hemp 0.39 0.09 0.58 1.06 Indigenous
Aglaia rimosa Meliaceae Balubar 0.16 0.08 1.16 1.40 Threatened/indigenous
Alnus japonica Betulaceae Japanese alnus 6.19 15.60 2.33 24.12 Exotic
Alphitonia philippinensis Rhamnaceae Tulo 6.04 2.09 2.33 10.45 Endemic
Archidendron merrillii Fabaceae Anagap-bangin 0.31 0.15 0.58 1.04 Endemic
Astronia benguetensis Melastomataceae Benguet dungao 0.24 0.29 1.74 2.27 Endemic
Astronia glauca Melastomataceae Dungau-puti 0.27 0.21 1.16 1.64 Endemic
Beilschmiedia purpurea Lauraceae Magansira 0.12 0.09 0.58 0.79 Indigenous
Breynia cernua Phyllanthaceae Matang-katang 1.14 0.77 1.74 3.65 Indigenous
Breynia racemosa Phyllanthaceae Karmai-bugkau 1.49 0.46 0.58 2.53 Endemic
Breynia rhamnoides Phyllanthaceae Matang-hipon 1.06 0.36 2.33 3.75 Indigenous
Callicarpa magnifolia Lamiaceae Agnai 0.16 0.10 1.16 1.42 Endemic
Callicarpa subintegra var. parva Lamiaceae Taringau-liitan 3.02 1.40 2.91 7.33 Indigenous
Clerodendrum klemmei Lamiaceae Luag 0.04 0.03 0.58 0.65 Endemic
Clerodendrum pubifolium Lamiaceae Bagauak-mabolo 0.04 0.06 0.58 0.68 Indigenous
Clethra canescens var. luzonica Clethraceae Apiit 0.20 0.15 0.58 0.93 Endemic
Cyathea contaminans Cyatheaceae Tree fern/pakong
buwaya
0.94 1.05 0.58 2.57 Vulnerable
Dacryodes incurvata Burseraceae Kamingi 0.16 0.10 0.58 0.84 Indigenous
Dacryodes rostrata Burseraceae Lunai 0.31 0.17 1.16 1.65 Indigenous
Ehretia acuminata Boraginaceae Tanaua 0.31 0.54 1.16 2.02 Indigenous
Elaeocarpus bontocensis Elaeocarpaceae Kalumbaya 0.04 0.01 0.58 0.63 Endemic
Elaeocarpus multiflorus Elaeocarpaceae Tigalot 0.16 0.03 0.58 0.77 Indigenous
Engelhardtia spicata var.
colebrookeana
Juglandaceae Pedped 8.08 2.91 3.49 14.48 Indigenous
Engelhardtia spicata var. spicata Juglandaceae Lupisan 0.20 0.20 1.16 1.56 Indigenous
Eucalyptus pellita Myrtaceae Red mahogany 0.43 1.23 0.58 2.24 Indigenous
Eurya buxifolia Theaceae Basbasit 3.25 3.04 2.91 9.20 Indigenous
Evodia dubia Rutaceae Sidi-sidi 1.10 0.79 0.58 2.47 Endemic
Fagraea auriculata Loganiaceae Curran urung 0.24 0.21 1.16 1.61 Endemic
Ficus annulata Moraceae Siningsing 5.61 2.91 3.49 12.00 Indigenous
Ficus heteropoda Moraceae Alangas 0.16 0.30 1.16 1.61 Endemic
Ficus nota Moraceae Tibig 0.08 0.13 0.58 0.79 Indigenous
Ficus pseudopalma Moraceae Niog-niogan 0.20 0.14 1.16 1.50 Endemic
Ficus pungens Moraceae Isis-tilos 0.31 0.13 2.33 2.77 Indigenous
Ficus ruficaulis Moraceae Tabgun 0.39 0.12 0.58 1.09 Indigenous
Ficus satterthwaitei Moraceae Malatibig 0.39 0.25 1.16 1.80 Indigenous
Ficus septica Moraceae Hauili 2.43 2.70 3.49 8.62 Endemic
Glochidion urophylloides Phyllanthaceae Halakan 0.43 0.21 1.74 2.38 Endemic
Gmelina arborea Lamiaceae Gmelina 1.29 2.60 1.16 5.06 Exotic
Grewia setacea Tiliaceae Alinau 0.74 0.22 1.16 2.13 Uncertain
Guioa reticulata Sapindaceae Alahan-sinima 0.35 0.10 0.58 1.03 Critically endangered/
Endemic
Helicia graciliflora Proteaceae Salimai-liitan 0.04 0.06 0.58 0.68 Endemic
Heptis sp. Lamiaceae 0.04 0.01 0.58 0.63
Homalanthus alpinus Euphorbiaceae Buta 0.35 0.09 0.58 1.03 Endemic
Homalanthus populneus var.
populneus
Euphorbiaceae Balanti 0.94 1.43 1.74 4.12 Indigenous
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diversity index (Shannon–Wiener index) of a Rhizophora
stand in Verde Passage in San Juan, Batangas, Philippines
is 0.8165–1.4185, with a total of nine species identified.
Bacudo et al. (2006) identified 86 floral species belonging
to 43 families in four quadrats established in Mindoro State
College of Agriculture and Technology (MinSCAT) forest
reservation, Mindoro Province, Philippines. The most
dominant species was Pometia pinnata, a member of the
family Santalaceae, with importance value of 5.41 %,
while Donax cannaeformis was the most dominant herb
plant species, with 4.86 % importance value. The diversity
index (Shannon–Wiener index) ranged from 2.8113 to
3.2715. The Alno communal forest is still diverse, as
indicated by the high diversity index of 3.2129 and 2.3870
for the overstory and understory vegetation, respectively.
Spatial mapping and database
All trees found inside the established quadrats were map-
ped, and a database was also created (Fig. 3). Each tree
corresponds to one point and bears complete information
on its common name, family name, scientific name, height,
and DBH. In this way, forest managers can easily view and
evaluate the existing condition of the communal forest.
Table 2 continued
Scientific name Family name Local name RD RH RF IV Status/endemism
Lantana camara Verbenaceae Coronitas 0.31 0.14 1.16 1.61 Exotic
Leea congesta Leeaceae Kahig-inulo 0.63 0.58 0.58 1.79 Endemic
Leptosolena haenkei Zingiberaceae Panawil 0.12 0.06 0.58 0.76 Endemic
Lithocarpus luzoniensis Oleaceae Kilog 0.12 0.14 0.58 0.84 Endemic
Litsea ampla Lauraceae Marang-laparan 0.08 0.02 0.58 0.68 Endemic
Lygodium flexuosum Lygodiaceae Nito 0.04 0.02 0.58 0.64 Endemic
Maesa sp. Myrsinaceae 2.74 0.91 2.33 5.98 Indigenous
Melastoma malabathricum Melastomataceae Malatungaw 8.15 3.25 2.91 14.31 Indigenous
Melicope triphylla Rutaceae Matang-araw 0.31 0.17 1.74 2.23 Endemic
Pinanga philippinensis Arecaceae Bungang-dakigan 0.04 0.02 0.58 0.64 Endemic
Pinus kesiya Pinaceae Benguet pine 21.60 39.10 3.49 64.19 Indigenous
Pittosporum ramosii Pittosporaceae Albon/tungtunga 1.92 0.66 2.33 4.90 Endemic
Praravinia loheri Rubiaceae Loher-siganog 1.88 1.77 2.33 5.98 Endemic
Psidium guajava Myrtaceae Guava 4.12 1.90 2.91 8.92 Endemic
Saurauia bontocensis Actinidiaceae Deguai 0.74 0.48 1.16 2.39 Vulnerable
Saurauia elegans Actinidiaceae Uyok 0.20 0.20 1.16 1.56 Indigenous
Saurauia papillulosa Actinidiaceae Papayang 0.04 0.07 0.58 0.69 Endemic
Schefflera elliptica Araliaceae Galamay-amo 0.20 0.06 0.58 0.84 Uncertain
Scurrula atropurpurea Loranthaceae Dapong kahoy 0.12 0.09 0.58 0.79 Indigenous
Spiraeopsis celebica Cunoniaceae Bognag 0.47 0.12 0.58 1.17 Indigenous
Symplocus ophirensis Symplocaceae Sotsa 0.20 0.05 0.58 0.82 Indigenous
Tristiropsis acutangula Sapindaceae Gasi-gasi 0.59 0.65 1.16 2.40 Indigenous
Vaccinium sp. Ericaceae 0.39 0.27 2.33 2.99 Indigenous
Vernonia acrophylla Asteraceae Adasay 0.12 0.06 0.58 0.76 Endemic
Viburnum cornutidens Caprifoliaceae Tilba 0.51 1.05 0.58 2.14 Indigenous
Viburnum glaberrimum Caprifoliaceae Apit 0.04 0.01 0.58 0.63 Endemic
Viburnum odoratissimum Caprifoliaceae Idog 0.43 0.37 1.16 1.97 Indigenous
Viburnum platyphyllum Caprifoliaceae Apit-laparan 0.63 0.81 1.74 3.18 Endemic
Weinmannia luzoniensis Cunoniaceae Itangan 1.06 1.56 1.16 3.78 Endemic
Wendlandia philippinensis Rubiaceae Mamboi 0.04 0.02 0.58 0.64 Endemic
Wendlandia uvariifolia Rubiaceae Karimbabui 0.08 0.01 0.58 0.67 Indigenous
Wendlandia warburgii Rubiaceae Rado 1.88 1.59 2.91 6.38 Endemic
Zanthoxylum avicennae Rutaceae Kangai 0.24 0.04 0.58 0.85 Indigenous
Total 100.00 100.00 100.00 300.00
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Table 3 Diversity index of
grass, herbs, and ferns in Alno
communal forest using the line
intercept method
Scientific name Family name Local name No. of individuals Status/endemism
Ageratina adenophora Asteraceae Bebengtet 94 Common
Anamirta cocculus Menispermaceae Lagtang/libtang 3 Vulnerable
Centella asiatica Apiaceae Takip-kuhol 4 Common
Chromolaena odorata Asteraceae Hagonoy 80 Uncertain/exotic
Christella dentata Thelypteridaceae Pako 12 Indigenous
Curculigo capitulata Hypoxidaceae Abang-abang 1 Common
Davallia sp. Davalliaceae 7 Indigenous
Desmodium trifolum Papilionaceae Pakpak langaw 10 Indigenous
Dicranopteris linearis Gleicheniaceae Kilob 11 Not threatened
Digitaria sanguinalis Poaceae Hairy crab grass 40 Indigenous
Digitaria velutina Poaceae Velvet crabgrass 44 Common
Elephantopus tomentosus Asteraceae Tabtabako 106 Endemic
Embella philippinensis Myrsinaceae Dekay/lando 4 Endemic
Eupatorium sp. Asteraceae Sipa-sipa 469 Common
Fimbristylis sp. Poaceae 2 Common
Globba campsophylla Zingiberaceae Luya-luyahan 6 Endemic
Hyptis suaveolens Lamiaceae/Labiatae Bangbangsit 3 Vulnerable
Imperata cylindrica Poaceae Cogon 99 Common
Lantana camara Verbenaceae Coronitas 10 Exotic
Leptosalena haenkei Zingiberaceae Panawil 1
Lygodium flexuosum Lygodiaceae Nito 1 Endemic
Mikania cordata Asteraceae Uoko 79 Common
Miscanthus sinensis Poaceae Rono 65 Common
Paspalum conjugatum Poaceae Kulape 386 Common
Passiflora edulis Passifloraceae Pasionaria/masaplora 1 Exotic
Pteridium aquilinum Dennstaedtiaceae Bracken fern 29 Common
Pteris tripartita Pteridaceae Giant bracken fern 15 Common
Rubus fraxinifolius Rosaceae Sapinit 15 Threatened/endemic
Scleria scrobiculata Cyperaceae Sarat 7 Indigenous
Urena lobata Malvaceae Kollo-kollot 16 Common
Asteraceae Inangel 63
Total 1,683
Diversity index, H02.387
Fig. 3 Map showing the trees
identified in quadrat 1 and
its database
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Acknowledgments The authors gratefully acknowledge the Jaime
V. Ongpin Foundation Inc. for funding this study. Special thanks are
also given to the College of Forestry-Benguet State University for
allowing us to conduct this research. This study was also carried out
with the support of Forest Science and Technology Projects (project
no. S211012L020410) provided by the Korea Forest Service.
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... According to the national list of threatened Philippine plants, S. bontocensis is a vulnerable species (DAO 2017-11), which could be due to a high rate of deforestation in its distribution range, the Cordillera Region (Daipan and Franco 2022). It is most commonly found in the provinces of Abra, Benguet, Mountain Province, Kalinga, and Ifugao (Pelser et al. 2011;Malabrigo 2013;Lumbres et al. 2014;Subilla and Baoanan 2021). Saurauia polysperma, on the other hand, is mostly found in the provinces of Ilocos Norte, Benguet, La Union, Nueva Viscaya, Pampanga, and Bataan (Pelser et al. 2011). ...
... and Gordonia polysperma Blanco (Pelser et al. 2011;Govaerts et al. 2021; Kew Royal Botanic Gardens Plant of the World Online (POWO)). Malabrigo (2013), Taguiling (2013) and Lumbres et al. (2014), mentioned the occurrence of S. bontocensis in their floristic assessment studies and they were all referring to the deguia / dagwey tree, the commonly used name of the species. This was also observed in the papers of Subilla and Baoanan (2021) and Tacloy et al. (2022) wherein they referred to deguia as the common name of S. bontocensis. ...
... This was also observed in the papers of Subilla and Baoanan (2021) and Tacloy et al. (2022) wherein they referred to deguia as the common name of S. bontocensis. Other local names for this species include dogdoguay in 3870 Abra; deguay in Bontoc (Merrill 1914); dagway, deguia, dogwe in Ifugao (Balangcod and Balangcod 2009;Taguiling 2013); deguai in Benguet (Lumbres et al. 2014;Tacloy et al. 2022); dagwey (in Ikalahan) Nueva Viscaya (Rice 2002); and dagwey in Kalinga (Malabrigo 2013). However, in the paper of Fabelico (2020) on the phytochemical, antioxidant, cytotoxic, and antimicrobial properties of the endemic dagwey, he used the taxon S. subglabra, which is a synonym for S. polysperma, to refer to the dagwey tree. ...
Article
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Major confusion still exists among several authors concerning the taxonomy of the dagwey plant. This species is economically significant to the Ikalahan tribe of Luzon, Philippines. Several papers claimed that the plant is Saurauia bontocensis, while others stated that it is Saurauia subglabra. Many botanical websites claimed that S. subglabra is synonymous with S. polysperma, while another article distinguished S. subglabra from S. polysperma. Thus, to help resolve the taxonomic ambiguities, this paper performed a comparative analysis of the leaf architectural characters of S. bontocensis and S. polysperma with the aid of digital image analysis software and cluster analysis. Results revealed that the blade characters alone, delineate the two species, particularly, in terms of the laminar size, shape, symmetry, leaf L:W ratio, base and apex angle, and base shape. Additionally, the leaf venation characters delineate the two species, specifically, on the 2º to 5º vein categories, 2º vein angle, 3º vein course, 3º vein angle to 1º, areolation, freely ending ultimate veins, marginal ultimate venation, and leaf rank. Generally, S. bontocensis have larger, longer, and wider leaves compared with the S. polysperma. The leaf architecture analysis performed in this paper produced a very promising result in differentiating the two Saurauia species and could be used to address some of the taxonomic confusion of these species. The study indicated that S. bontocensis and S. polysperma are two distinct species. Moreover, the use of digital image analysis software was very helpful in the computations of the various blade characters, particularly the digital herbarium exsiccate in the absence of actual leaf samples.
... The ecological, social and climate change aspects of tropical communal forests have been studied by some authors (eg. Lumbres et al., 2014;Chechina et al., 2018;Hugé et al., 2022) but often, these were tackled singly and not collectively. Rader et al. (2024) stressed the data gap on the interplay of ecology and biodiversity conservation, considering social and economic aspects, and recommended more studies on these for sustainable future. ...
... The difference could be attributed to sampling intensity and focus since the previous inventory only involved three plots and focused on trees while the current inventory placed equal focus on trees, shrubs and herbs. Our result is also much higher compared to results of Lumbres et al. (2014) in the nearby Alno Communal Forest with 78 species under 43 families. Compared to other recent floral inventories in CCR, our result was also higher than the 68 species under 63 genera and 40 families documented by Guron et al. (2019) in Talinguroy Research Station, La Trinidad; the 61 species under 25 families by Batani et al. (2023) in Palina River, Kibungan; and the 52 species under 40 genera and 31 families by Rabena et al. (2015) in a muyong forest in Ifugao. ...
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Communal forests are recognized to be of critical importance for the attainment of sustainable development goals (SDGs) but these are often understudied. Such is the case in Cordillera Central Range with its unique biodiversity and urban biodiversity sites requiring protection like the Alapang Communal Forest in Benguet, Northern Philippines. This study documented the floral diversity, carbon stock and the community perspectives as baseline for conservation. A total of 187 plant species belonging to 145 genera and 70 families were recorded with Pinus kesiya as the most dominant species. The forest exhibited high species richness, evenness, and diversity including indigenous, endemic species and some conservation important species. The total forest carbon was estimated at 6,931.44 t with an average of 192.54 t/ha. An interesting trade off was documented in the study with the pine dominated ridge stations having lower diversity but higher carbon stock while broad-leaf dominated depressed stations have higher diversity but lower carbon stock. Community surveys revealed the willingness to protect the forest due to its crucial role as a water source, highlighting its value and the importance of preservation. These findings offer empirical evidences on the role of communal forest on biodiversity conservation, carbon stock as well as forest goods and services. Locally, these findings offer insights for conservation and sustainable management of the Alapang Communal Forest and other local urban forests.
... This could be directly attributed to the more extensive inventory or sampling conducted in the former studies compared to the later studies. Also, equal attention to the understory and overstory (tree) inventory was performed unlike the inventory of Lumbres et al. (2012) and Rabena et al. (2015) that focused primarily on trees. In this study, we found that the species richness in the understory (herb and shrub combined) is much higher than the tree species. ...
... The biodiversity indices of Kennon Road summarized in Table 3 is comparable with those recorded by Dulnuan and Napaldet (2023) in Amburayan River with Shannon index of 4.48, an evenness index of 0.57, Simpson's index at 0.97, and a Margalef's index of 31.32; and by Balangen et al. (2023) in Tadiangan, Tuba with 3.73 -4.24 Shannon index. Our results are also comparable with the results of Guron et al. (2019) in Talinguroy Research Station and Lumbres et al., (2012) in Alno Communal Forest. Consistently, the herb diversity values are much higher than the shrub and tree diversity in all sampling stations. ...
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Mountain roads are constructed to spur economic development and alleviate poverty but they are also major drivers of biodiversity loss in mountain areas. In the Philippines, road biodiversity is poorly understood. This study aims to contribute to this gap by presenting the plant diversity along Kennon Road, a national highway in Benguet, Philippines through population counts, biodiversity indices and floristic elements. A total of 338 species belonging to 280 genera and 99 families were inventoried in five sampling stations. Majority of the plant species were indigenous (186) with 35 endemic, 29 naturalized, 88 exotic species and with 18 threatened species (5.33% of the total species). Understory plants have the highest biodiversity indices, particularly Shannon index ranging from 3.49 to 3.93 (very high diversity). On the other hand, Shannon values for shrub ranges from 2.97 (moderate) to 3.51(very high) and least Shannon values were derived from tree diversity at 2.54 (moderate) to 3.31 (high). The floristic elements along Kennon Road are dominated by native (76.33%) but a significant part (23.675) of the vegetation are either naturalized or exotic with mostly Central American and Neotropical elements. Our results show the fragmentation of the secondary forest along the road with human built-up areas and the colonization by ruderal species including non-native species.The intermingling of these colonizers with resident species results in the formation of forest road ecosystems with high species richness in Kennon Road.
... This could be directly attributed to the more extensive inventory or sampling conducted in the study compared to these studies. Also, we also focused equal attention to the understory and overstory (tree) inventory unlike the inventory of Lumbres et al. (2014) and Rabena et al. (2015) that focused primarily on trees. In this study, we found that the species richness in the understory (herb and shrub combined) is much higher than the tree species. ...
Article
This study inventoried the floral diversity of a secondary forest in Tuba, Benguet, Philippines as affected by different intensities of human disturbance. This study is unique from other land use studies in Southeast Asia in having conventional farms as the most disturbed land use while other sites have oil palm plantations. A total of 267 species belonging to 222 genera and 78 families was documented. Results showed that the level of human disturbance is the major factor affecting the floral diversity while the effect of elevation is secondary. The level of human disturbance is significantly associated with species richness, species composition, dominant species and biodiversity indices. Greater human disturbance, as in the case of conventional farms, results in lower species richness, predominantly weed composition, dominant weed species and lower biodiversity indices. On the other hand, lesser human disturbance (as in the case of secondary forest) leads to higher species richness, greater native species composition, dominance of indigenous species, and higher diversity indices. The most disturbed land use experienced the greatest loss of species richness, change in floristic composition and vegetation structure, as well as a shift from native to alien-dominated plant communities. These results showed that the effect of land use change is not limited to species richness but also to species composition, dominant species and biodiversity indices. Locally, the study is an important baseline data for biodiversity conservation of the Marcos Highway Watershed Forest Reserve.
... Our results are more comparable but still higher than the results of Batani et al. (2019) in Palina River, Kibungan, which recorded Shannon-Wiener's of 3.39, evenness of 0.60, Simpson's of 0.94 and Margalef's index of 10.59. Furthermore, the study's findings are comparable to those of Guron et al. (2019) in Talinguroy Research Station and Lumbres et al. (2012) in Alno Communal Forest. ...
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Agricultural activities are known to have significant implications on floral diversity and edaphic condition of riparian ecosystems but the data base to elucidate this phenomenon in the tropical semi-subsistence agriculture setting is insufficient. This study documented the floral diversity and edaphic conditions in the riparian zones of Amburayan River, Northern Philippines as exposed to varying intensities of agricultural activities. A total of 249 vascular plant species belonging to 200 genera and 74 families were documented. Greater agricultural disturbance resulted to lower indigenous and endemic species, lower overall species diversity, lower shrub and tree diversity, but higher herb diversity. In terms of edaphic factors, the soil pH ranges from moderately to slightly acidic (5.37–6.43) while soil texture ranges from loamy sand and sandy loam. The soil organic carbon is lowest in the intensely disturbed stations and highest in less disturbed stations while soil moisture content is significantly higher in the less disturbed stations than in intensely and moderately disturbed stations. Lastly, the soil nutrients, N, P and K range from 0.04–0.36 mg/kg, 4.13–64.90 mg/kg and 86.67 to 253.33 cmol/kg, respectively. The study found significant correlations between the soil condition, agricultural disturbances and floral diversity of Amburayan River. These findings illustrate for the first time in available literature the mosaic interplay of intensity of disturbance, elevation and soil properties with floral diversity in riparian ecosystem under a tropical semi-subsistence agriculture setting.
... The high number of individuals of Benguet Pine was expected, given that this species is restricted in the northern part of Luzon, mainly in Benguet, Philippines. Other research studies, such as the study in Benguet, also found P. kesiya as the most dominant species in the forest ecosystem surveyed (Lumbres et al., 2014). ...
Article
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The paper shows the floristic species composition, structure, and diversity, including the ecological importance of the portion of Lower Agno Watershed Forest Reserve. Through quadrat and transect surveys, this study assessed six forest ecosystems, three grassland ecosystems, and five riparian sites. There were 41 tree species, 91 understorey species, 87 ground cover species, and 69 riparian species. Dominant species include Pinus kesiya Royle ex. Gordon, Chromolaena odorata (L.) King, Miscanthus sp., Wikstroemia ovata C.A. Mey ex Meisn, Ayapana triplinervis (Vahl) R.M. King & H. Rob, Leucaena leucocephala (Lam.) de Wit, Saccharum spontaneum L., and Lantana camara L. Forest ecosystems had secondary growth trees with a mean diameter ranging from 17 to 43 cm and mean height of 10 to 18 m. Results showed that the area was moderately diverse, with H' ranging from 2.26 to 2.90 and having a similarity index ranging from 0 to 50%. The site was ecologically important, home to 47 natives, nine endemic, nine internationally threatened, and four nationally threatened species. Regarding soil and plant nutrients, the values obtained were within the normal range for N, P, and K except for Alnus japonica (Thunb.) Steud. which acted as an accumulator with very high Cu content (53 ppm), making it an essential species in rehabilitating areas dominated by highly mineralized soil. Results could serve as baseline information vital in devising conservation and protection strategies to manage better and preserve the site.
... Total Stand Basal Area (m 2 /ha) = Sum of basal area for each tree 0.04 = Sum of basal area × 25 (6) where 0.04 is plot size in hectare and 25 is a constant used to extrapolate the measurement of the basal area from per plot (m 2 /plot) to per hectare (m 2 /ha). The Species Diversity index, determined in this study using the Shannon-Wiener's Index [25], indicated a quantitative description of mangrove habitat in terms of species distribution and evenness; this species diversity index was used in several studies [26][27][28] and was calculated using the following form: ...
Article
Full-text available
Mangrove ecosystems sequester and store large amounts of carbon in both biomass and soil. In this study, species diversity, the above and below-ground biomass as well as carbon stock by the mangroves in Kanhlyashay natural mangrove forest were estimated. Six true mangrove species from four families were recorded in the sample plots of the study area. Among them, Avicennia officinalis L. from the Acanthaceae family was the abundance of species with an importance value of 218.69%. Shannon–Wiener’s diversity index value (H0 = 0.71) of the mangrove community was very low compared to other natural mangrove forests since the mangrove stands in the study site possessed a low number of mangrove species and were dominated by a few species. Estimated mean biomass was 335.55 ± 181.41 Mg ha−1 (AGB = 241.37 ± 132.73 Mg ha−1, BGB = 94.17 ± 48.73 Mg ha−1).The mean overall C-stock of the mangrove stand was 150.25 ± 81.35 Mg C ha−1 and is equivalent to 551.10 ± 298.64 Mg CO2 eq. The role of forests in climate change is two-fold as a cause and a solution for greenhouse gas emissions. The result of the study demonstrated that the mangroves in Letkhutkon village have high carbon storage potential, therefore it is necessary to be sustainably managed to maintain and increase carbon storage. Climate change mitigation may be achieved not only by reducing the carbon emission levels but also by maintaining the mangrove ecosystem services as carbon sinks and sequestration.
... vegetation assessed in Alno communal mixed forest in Benguet (Lumbres et al. 2014) and in Balbalasang-Balbalan National Park in Kalinga (Malabrigo Jr. 2013 ...
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Understanding the species distribution patterns of endemic and threatened species is very useful for conservation planning and actions. However, research on the distribution of many important and often overlooked species in the country, such as the Saurauia, is extremely limited. This paper provided an overview of the distribution patterns of Saurauia species across the Philippine archipelago based solely on the existing digital checklist of vascular plants. Specifically, the study produced distribution maps of the 56 endemic Saurauia species and determined their climatic distribution ranges. The methods involved geospatial and geoprocessing analysis in a geographic information system (GIS) environment. The findings showed that 29 Saurauia species are currently distributed in a single province, whereas seven (7) species have only been recorded in a certain region. Furthermore, 35 species was found to have a single type of climate. The Saurauia species identified in this paper that have only a single provincial or regional distribution record and are restricted to a single type of climate are recommended for conservation because they are mostly likely to be affected by environmental and climatic changes. Finally, the information and data derived in this paper could serve as a baseline for assessing conservation status, habitat modelling studies, species-level conservation planning, and understanding climate change impacts.
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Mangrove ecosystems play crucial roles in promoting biodiversity and mitigating climate change impacts by serving as habitat for marine life and sinks of atmospheric carbons. The Verde Passage Corridor which fringes the province of Batangas, Philippines has a huge potential for both biodiversity conservation and carbon sink development because of its extensive coastal areas that can be developed into mangrove forest. This opportunity is exemplified in the case of rhizoporas, locally known as bakcnvan, in San Juan, Batangas where this study was conducted. Using the nested plot sampling method developed by Hairiah et al. (2001), the study assessed the diversity (H') and carbon density of the stand Diversity index (H'= 0.8165 to 1.4185) is very low with a total of nine species recorded Despite of lean diversity, bakawan stand was still regarded healthy and vigorous in mitigating the impacts of climate change because of its huge carbon density estimates. Carbon density was estimated to be around 115.45 t ha(-1).
Book
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The standard textbook of Vegetation Ecology. A reprint (2002) is available from The Blackburn Press, Caldwell, New Jersey.
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Recent fieldwork of the Royal Botanic Gardens, Kew, in many parts of the tropics reveals the extent to which they are still undercollected and poorly studied. Recent studies of palms in Madagascar, Cameroon, Lao P.D.R., and Brunei Darussalam have produced many novelties, for example, in Madagascar, 3 new genera and 85 new species. Recent examples from Atlantic coastal Brazil, central Amazonia, and New Guinea are given. Even in apparently well collected areas such as the Ducke Forest Reserve near Manaus, Brazil, and in Brunei where detailed studies of small areas are made, many novelties are found. It is recommended that more such intensive studies of restricted areas are made. The rate of new species that are being described, an average of 2350 over the past nine years, and the rate of additions to Flora Neotropica suggest that the total number of angiosperms is currently being underestimated and that there are in fact between 300,000 and 320,000 species. In order to develop conservation and sustainable use of tropical ecosystems, it is essential that we continue to intensify the rate of collection before it is too late.
Article
An exhaustive floristic inventory was conducted in a 400-ha block of tropical semideciduous forest in the Chiquitanía region of Santa Cruz, Bolivia. A total of 501 species were collected using both quantitative and traditional plant collecting methods. Trees represented the most diverse life form (124 spp), followed by herbs (101 spp), lianas (85), shrubs (66), herbaceous climbers epiphytes (15) and parasites (two). Floristic diversity was greatest for the forest floor community, when compared to either the understorey or canopy tree communities. Quantitative data were obtained for 336 species in 100 plots which contained a series of nested subplots to sample smaller-stature plants. Stem density for trees (dbh[greater-than-or-equal]5 cm) was 914 trees ha[minus sign]1, with a total density for all life forms estimated to be 135,000 plants ha[minus sign]1; the total basal area for the forest was estimated to be 27.6 m2 ha[minus sign]1. Species richness when measured by standard methods was found to be one of the highest for a dry forest region reported for the Neotropics with a mean of 70.8 spp 0.1 ha[minus sign]1 (dbh [greater-than-or-equal] 2.5 cm) and 50 spp ha[minus sign]1 (dbh [greater-than-or-equal] 10 cm). Comparison of life forms and vertical strata showed that the flora on the forest floor was more diverse than all other vertical strata combined. Habitat heterogeneity was studied using ordination procedures based on floristic data and to identify the characteristic species of three plant communities: granite outcrops, valley forest and upland forest. The most abundant tree species in the study area were Acosmium cardenasii, Neea hermaphrodita, Aspidosperma tomentosa and Galipea trifoliata, while the species with the greatest basal area were Anadenanthera colubrina, Acosmium cardenasii, Caesalpinia floribunda, Aspidosperma tomentosa, Piptadenia viridiflora, Chorisia speciosa, Tabebuia impetiginosa, Centrolobium microchaete, and Machaerium scleroxylon. Most canopy and understorey tree species had a population structure characterized by numerous juveniles and relatively few large trees, while emergent species tended to have a size-class distribution with relatively few juvenile individuals. Lianas and canopy trees were predominantly anemochorous, while understorey trees and shrubs were predominantly zoochorous; herbaceous species were largely autochorous, with only fern species relying on wind dispersal (sporochory). A comparison of structural attributes with other dry forest areas in the Neotropics, demonstrates the heterogeneous nature of vegetation types that are commonly assigned to this ecosystem. The Chiquitano dry forest shares many floristic elements with the semideciduous forests of the Andean piedmont of northwestern Argentina, the Misiones region of eastern Paraguay and northeastern Argentina, as well as the Caatinga region of northeastern Brazil.
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The species diversity of broad-leaved trees in relation to the distance from a broad-leaved forest was investigated in Cryptomeria japonica plantations with crown snow damage near the Japan Sea in central Japan. The number and diversity of species and stem density decreased with distance from the broad-leaved forest in maturing gap stands (51–58 years old; >10 years after crown snow damage), but not in recent gap stands (34–42 years old; <10 years after crown snow damage), and increased with improved light conditions in the interior of recent gap stands, but not in that of maturing gap stands. The stem densities of tall and small tree species and woody lianas were greater in the interior of recent gap stands than in maturing gap stands. Woody lianas, which are characteristically shade intolerant, had a high stem density in the interior of recent gap stands. In contrast, the stem density of shrubs was greater in maturing gap stands than in recent gap stands, irrespective of distance. Shade-tolerant shrubs had a high stem density in maturing gap stands. Wind-dispersed and frugivore-dispersed species were concentrated at the edges of maturing gap stands, but some frugivore-dispersed species, which may persist in soil seed banks, occurred in the interior of recent gap stands. Gravity-dispersed species tended to occur both at the plantation edge and in the interior. The differences in the occurrence patterns of broad-leaved trees in the two types of stands reflected the difference in the effect of both the distance from the adjacent broad-leaved forest and the light conditions related to canopy gaps, with the time since gap formation in a region where crown snow damage often occurs.
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We investigated effects of silvicultural treatments (planting and subsequent treatments) on understory structure and plant species diversity in managed Picea glehnii plantations (21–26 years old) in northern Japan. We evaluated the importance of each treatment (machinery site preparation, planting, weeding, and thinning) in 19 plantations, with considerable variation among treatments overall. The understory had 98 vascular plant species; the most dominant species was a dwarf bamboo Sasa senanensis, followed by tree species Abies sachalinensis and Betula ermanii. Multiple regression analyses showed that thinning negatively influenced plant species diversity. Planting density showed a strong positive correlation with density of seedlings (height <20 cm), but few independent variables were correlated with density of saplings (height ≥20 cm and diameter at breast height <1 cm). The negative effect of thinning and the positive effect of planting density seem to be related to the existence or reinitiation of dense cover of Sasa senanensis. We present possible mechanisms of response to treatments to generalize the results. We then suggest ways to improve current treatments to meet the goals of wood production and biodiversity conservation in the region.
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Biodiversity in Asia is reviewed here from both scientific and socio-economic perspectives. Biodiversity in Asia has been very high, for historical and climatic reasons; however, this situation has been changing rapidly, due to population growth and economic development. The forest biodiversity in this region has both global and local value, yet it is seriously threatened. As natural capital, biodiversity functions in a variety of ways: production and regulation functions have global value, while habitat and information functions have social and cultural value, as well as local importance. Sustainable forest management is dependent on the regulatory functions of the ecosystem and biodiversity. Sometimes the functions of forests or biodiversity make conflict. Moreover, biodiversity has an information function related to sustainability via local knowledge and culture. Levin’s (1999) proposals are helpful as a conceptual framework for developing sustainable management for Asian forests.
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The assessment of biodiversity in managed plantations has become an important issue for long-term sustainability of the ecosystem. The continuous cropping system (CCS) is common practice in Eucalyptus plantations in southern China. In order to clarify the effects of such a practice on species compositions, species diversity, and functional type compositions of understory vegetation, a field trial was installed in the first and second rotations of Eucalyptus plantations. The treatments were replicated three times and arranged in a simple completely randomized design. Vegetation surveys were performed in 1998–2005 following the treatments. Although the CCS had no significant effect on the composition structures in terms of life-form, growth-form, seed dispersal strategies and breeding strategies, there were significant differences in percent coverages of shrub (SLC) and herbaceous layer (HLC) between two types of stand. The CCS reduced the species richness and species diversity remarkably, and was also particularly favorable for r-strategy herbaceous species at the expense of k-strategy woody species in understory vegetation. The repeated disturbances to soil and vegetation including clear-cutting followed by prescribed burning and mechanical plowing maybe the main factor which results in the negative change of understory plant diversity. Although more comprehensive studies on disturbance and a long-term monitoring of a broad-scale project will be required, we suggest that alternative silviculture, consisting of practices other than clear-cutting and prescribed burning, should be introduced to conserve species composition and diversity of Eucalyptus plantations. KeywordsContinuous cropping system- Eucalyptus plantation-Functional types-Species diversity-Vegetation structure