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Available online at www.worldscientificnews.com ( Received 26 October 2019; Accepted 18 November 2019; Date of Publication 20 November 2019 ) WSN 138(2) (2019) 192-224 EISSN 2392-2192 Temporal variation in species composition, diversity and regeneration status along altitudinal gradient and slope: The case of Chilimo dry Afromontane forest in the Central Highlands of Ethiopia Mehari A. Tesfaye 1,a , Oliver Gardi 2,b , Jűrgen Blaser 2,c 1 Central Ethiopia Environment and Forest Research Centre, Box 30708, Addis Ababa, Ethiopia 2 Bern University of Applied Sciences, School of Agriculture Forest and Food Sciences HAFL, CH - 3052, Zollikofen, Switzerland a-c E-mail address: [email protected] , [email protected] , [email protected] a Corresponding author: Mehari A. Tesfaye, Phone +251911356756, +251-0116-46044 ABSTRACT This study is aimed towards investigating the temporal variation in species composition, diversity and regeneration status of Chilimo dry Afromontane forest in the Central Highlands of Ethiopia. A total of 35 permanent sample plots of 20 m × 20 m (400 m 2 ) each were established in the natural forest, laid out on transects of altitudinal gradients, with a distance of 100m between plots. The plots were measured twice in 2012 and 2017. Three subplots, 5m × 5m, and 1 m 2 were laid out inside the main plots for sapling, shrub and seedling data collection. Species composition, diversity, important value index (IVI) and regeneration data were analyzed using appropriate formulas. Data analysis was made using R - studio software. A total of 31 trees and shrubs representing 25 families were recorded, 20 (64.52 %) were trees and 11 (35.48 %) were shrubs. Thereof, 28, 23 and 26 species under highest, middle and lowest altitudinal gradient were recorded. The most dominant tree species were: Juniperus procera, Podocarpus falcatus, Olea europea, Scolopia theifolia and Allophyllus abyssinicus. The species

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Page 1: Temporal variation in species composition, diversity and ...€¦ · mountains’ using a measuring tape, GPS and compass. The boundaries of the main plots were pegged and marked,

Available online at www.worldscientificnews.com

( Received 26 October 2019; Accepted 18 November 2019; Date of Publication 20 November 2019 )

WSN 138(2) (2019) 192-224 EISSN 2392-2192

Temporal variation in species composition, diversity and regeneration status along altitudinal gradient and slope: The case of Chilimo dry Afromontane

forest in the Central Highlands of Ethiopia

Mehari A. Tesfaye1,a, Oliver Gardi2,b, Jűrgen Blaser2,c

1Central Ethiopia Environment and Forest Research Centre, Box 30708, Addis Ababa, Ethiopia

2Bern University of Applied Sciences, School of Agriculture Forest and Food Sciences HAFL, CH - 3052, Zollikofen, Switzerland

a-cE-mail address: [email protected] , [email protected] , [email protected]

aCorresponding author: Mehari A. Tesfaye, Phone +251911356756, +251-0116-46044

ABSTRACT

This study is aimed towards investigating the temporal variation in species composition, diversity

and regeneration status of Chilimo dry Afromontane forest in the Central Highlands of Ethiopia. A total

of 35 permanent sample plots of 20 m × 20 m (400 m2) each were established in the natural forest, laid

out on transects of altitudinal gradients, with a distance of 100m between plots. The plots were measured

twice in 2012 and 2017. Three subplots, 5m × 5m, and 1 m2 were laid out inside the main plots for

sapling, shrub and seedling data collection. Species composition, diversity, important value index (IVI)

and regeneration data were analyzed using appropriate formulas. Data analysis was made using R -

studio software. A total of 31 trees and shrubs representing 25 families were recorded, 20 (64.52 %)

were trees and 11 (35.48 %) were shrubs. Thereof, 28, 23 and 26 species under highest, middle and

lowest altitudinal gradient were recorded. The most dominant tree species were: Juniperus procera,

Podocarpus falcatus, Olea europea, Scolopia theifolia and Allophyllus abyssinicus. The species

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composition, diversity, abundance, dominance and important value index significantly varied among

species, altitudinal gradient and slope. The diameter distribution was an inverted J - shaped distribution

pattern. The highest species richness and diversity index were found under middle altitudinal gradient,

while the lowest species richness and diversity index were found under the highest altitudinal gradient.

The mean annual volume increment ranged from 4.223 to 0.228 m3 ha-1 yr-1, while the basal area

increment varied from 0.85 to 0.020 m2 ha-1 yr-1. Among the sampled species, ten species had fair, 5 poor

and 14 species had no regeneration. In conclusion, the Chilimo dry Afromontane forest is suffering from

low recruitment and regeneration. Thus, appropriate forest management options should be implemented.

Keywords: Abundance, altitude gradient, Ethiopia, native species, population structure, saplings,

seedlings and shrubs

1. INTRODUCTION

The structure and function of the forest ecosystem are determined by the plant component

more than any other living component of the system [1]. The population structure is expressed

in terms of a number of individuals present in a particular diameter class and the distribution of

tree species. Understanding the growth status of forests is key for ecosystem stability [2].

Topography, soil, climate and geographical location influence the vegetation diversity of the

forest ecosystem [3].

Sustainable forest management requires forest inventories, in combination with modeling

tools, forest growth and sustainable harvesting or cutting plans [4]. Such systems are common

in many parts of the world [5]. However, they are scarce for Africa’s forest in general and

Ethiopian forests in particular.

The dry Afromontane forests are either mixed Juniperus - Podocarpus forests or

predominantly Podocarpus forests, both with an element of broad-leaved species. They occur

in both the northwestern and southeastern highlands, especially on the plateau of Oromia,

Tigray, Amhara and Southern Nations, Nationalities and Peoples Regional States (SNNP) at

altitudes from 1500 - 2700m [6].

Reports indicate that the deforestation rate amounts to 92,000 ha-1yr-1, while, new

plantation area change is about 18,000 ha-1yr-1 [7]. A majority of the high forests found in

Ethiopia are managed primarily for protection and conservation purpose, while, commercial

utilization is a secondary objective. The forestry administration at the Federal level has

classified 108 of the most important high forest areas totaling an estimated area of 2 million ha

as National Forest Priority Areas of the country. Over two thirds of these high forests are

heavily disturbed forest and need appropriate forest management. The estimated annual height

and diameter growth are very low [8].

Moreover, information on species diversity, population structure and regeneration are

scanty in the study area, except for a few studies by [9] and [10]. Sustainable forest management

is possible if adequate information is available in these regards [11] and [12].

Chilimo forest is one of the few remnants of dry afro-montane forest located in the Central

Highlands, Chilimo forest is composed of - Juniperus procera, Podocarpus falcatus, Olea

europaea, Scolopia theifolia, Rhus glutinosa, Olinia rochetiana and Allophylus abyssinicus [9],

[13] and [14]. In the last, [14] reported 33 different native species in 3 forest patches and [9]

reported 213 different plants species categorized into 83 families.

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Of these, 17 plant species are unique to the Chilimo forest. The forest is also found in the

nearby the capital city of Addis Ababa, easily accessible through all - weather road and having

old historical palaces inside it.

Due to continuous deforestation, the Chilimo forest cover has declined from 22,000 ha in

1982 to 6,000 ha in 1991 and 4,500 ha in 2016 [10] and [16]. As result, some plant species are

becoming endangered [9].

Thus, scientific knowledge on the regeneration of Chilimo forest is important for

conservation and restoration endeavors. However, this knowledge is scanty for most forests in

the country, except for a few works done for dry Afromontane forests, Acacia woodlands or

woodlands and exclosures in the country [16-20].

In the present study, the species composition, diversity, growth, yield and regeneration

status of Chilimo dry Afromontane forest is investigated. We hypothesized that there is

temporal variation in species composition, diversity, yield and regeneration status along

altitudinal gradient and slope. Growth and yield study were, therefore, done for the eleven most

common native species viz:- Allophyllus abyssinicus, Apodytes dimidiata, Juniperus procera,

Celtis africana, Ekebergia capensis,Olea europaea,Olinia rochetiana, Podocarpus falcatus,

Prunus africana, Rhus glutinosa and Scolopia theifolia, because these native tree species are

the most abundant and dominant tree species in the forest. Moreover, the study was socially

acceptable and economically important. Some of the species are under increased pressure due

to illegal cutting for fuelwood, construction wood, farm implements and charcoal [20].

Therefore, such studies had been conducted with the hypotheses that species composition,

diversity and the regeneration status of Chilimo dry Afromontane forest vary along altitudinal

gradient and slope factors. Thus, the intent of the study was: (i) To determine the relative

frequency, density, dominance and important value index of woody species in the study sites;

(ii) To investigate the growth and yield of 11 dominant and economically important native tree

species; (iii) To assess the natural regeneration status of seedlings, sapling and tree population

densities along altitudinal gradients, slope percent and forest patch.

2. MATERIALS AND METHODS

2. 1. Chilimo dry afro-montane forest

Chilimo dry afro - montane forest is geographically located at 38° 07′ E to 38° 10′ E

longitude and 9° 30′ to 9° 50’ N latitude at an altitude of 2,170 - 3,054 m asl (Figure 1) in Dendi

district, Western Shewa zone, Oromia Administrative Region, Central Highlands of Ethiopia.

The mean annual temperature of the area ranges between 15 – 20 ºC and receives mean annual

precipitation of 1000 - 1, 264 mm [10]. Köppen’s classification defines the climate of Chilimo

forest is classified as warm temperate climate I (CWB) type [21].

2. 2. Reconnaissance survey

A discussion forum held with Oromiya Wildlife and Forest Enterprise higher officials in

Addis Ababa for awareness creation and to get permission. Subsequently, a reconnaissance

survey was conducted through a field visit and physical observation across the Chilimo forest.

Then, 3 forest patches (Chilimo, Gaji and Gallessa) selected based on accessibility, species

composition and representativeness for further study. Inventory done starting from Chilimo

proceed to Gallessa and finally to Gaji forest patches.

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Figure 1. Sampling plots of Chilimo dry afromontane forest.

2. 3. Scheme of sample plot

A systematic sampling approach was implemented to conduct inventory. A total of thirty

- five, 20 × 20 m (20 in Chilimo, 11 in Gallessa and 4 in Gaji) squared sampled plots were

marked, based on Neyman optimal allocation formula in the natural forest [22]. The plots were

laid out along 100m ground distance, starting from the highest to the lowest ridges of the

mountains’ using a measuring tape, GPS and compass. The boundaries of the main plots were

pegged and marked, then altitude, slope, latitude and longitude data were recorded from the

center of each main plot. A total of ten transect lines (4 in Chilimo, 4 in Gallessa and 2 in Gaji)

were used along with an altitudinal gradient from top to bottom ridges of the mountain. The

distance between two consecutive transect lines was 300m to 1 km, depending on the

accessibility of the next transect. Sampling and data collection were done in the measured plots

of the mixed natural forest and plantation. Data collection was taken from October to

November 2012 and June to July 2017, respectively.

2. 4. Field data collection and sampling

Individual species were categorized into trees (≥ 5 cm diameter at breast height), shrubs

(dbh 5 to 2.5 cm), saplings (height ≥ 1.3 m and dbh 2.5 - 5 cm) and seedlings (height 0.30 - 1.3

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m and dbh ≤ 2.5 cm) following, Lamprecht classification [23]. Before actual measurements, all

bordering trees and shrubs were marked using red paints and numbered. Tree diameter (cm)

was measured using a metallic caliper for smaller and medium - sized trees, while, diameter

tape was used for bigger trees.

Total height (meter) was measured to the nearest two digits using Vertex III digital

electronics tree height measurement instruments. In cases, where trees branched at or below the

breast height, the diameter was measured separately for each branch and quadrado. Diameter at

each stem was measured separately for trees with multiple stems connecting near to the ground.

For irregularities and or buttresses on large trunks, measurement was taken at the nearest lower

point. In a similar way, each marked individual trees in 2012 was remeasured in 2017. Saplings

and shrubs were sampled inside each main plot on 3 subplots, 5m × 5m laid out diagonally.

Height and diameter were a measurement for saplings done using graduated wooden bars

and metallic caliper. While seedlings were sampled in 3 subplots, 1m x 1m, one at the center

and 2 in the edge of the diagonal, counting an average height measurement made using a

wooden ruler.

To study the growth and yield 11 trees species viz: - Allophyllus abyssinicus, Apodytes

dimidiata, Juniperus procera, Celtis africana, Ekebergia capensis, Olea europaea, Olinia

rochetiana, Podocarpus falcatus, Prunus africana, Rhus glutinosa and Scolopia theifolia were

selected based on their relative (frequency, density and dominance) and IVI. Moreover, visual

observation was done for some of the tree species based on their social acceptability and

economic importance.

2. 5. For growth and yield data

Basal area (BA) (m2 ha-1) and volume (Vt) (m3 ha-1) was calculated using inventoried data.

Total volume was calculated using the conventional volume equation because local volume

equations not available for these species:

V = 𝜋 (𝐷𝐵𝐻

4) 2 ∗ ℎ ∗ 𝑓 [24] ……………….. (eq.1)

where V: tree volume, DBH: diameter at breast height, h: total height, 𝑓: form factor (0.42) [24]

BA (Basal area) calculated using the formula:

BA = 𝜋𝐷𝐵𝐻2

4……………………………… (eq.2)

where BA: Basal area, DBH : Diameter at breast height, 𝜋: 3.142

Basal area and volume increment calculated as:

VtI = Vt2017- Vt2012…………………… (eq.3)

BAI = BA2017- BA2012……………… (eq.4)

where VtI: volume increment (m3 ha-1 yr-1 and BAI basal area increment (m2 ha-1 yr-1)

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3. DATA ANALYSIS

3. 1. Aboveground biomass

Aboveground biomass was calculated using [25] (eq. 5) because this equation is the most

recent and important predictive variables for estimation using diameter at breast height (DBH),

total height (H), basic wood density (ρ) and forest type.

AGBest = 0.0673(ρHD2)0.976…………………..… (eq.5)

where AGBest = above ground biomass (kg), D = DBH (cm), H = height (m), and ρ = basic

wood density (g·cm-3).

Accumulated above ground and below ground carbon density was calculated following

eq.6 and eq.7:

ACD = AGB ∗ 0.47 ……………………………… (eq.6) [26]

BCD = ACD ∗ 0.24 …………………………… (eq.7) [27, 28]

where ACD = Aboveground carbon density, BCD = Below ground carbon density.

The aboveground and below biomass for each tree was calculated separately in each plot,

then, the biomass of each tree was summed up to give plot biomass and converted into ha.

3. 2. Woody Speciesdiversity and structure analysis

The Species diversity was analyzed using the Shannon diversity index (H') [29] (eq.8):

Shannon-Wiener diversity index was calculated as

H'= - ∑ pi

s

i=1

lnpi ………………………........ (eq.8)

where; H' = Shannon - Wiener index of species diversity, pi = proportion of individual found

in the ith species and evenness were calculated using the following formula:

Equitablity (evennes) Equitability (evenness) J =H′

H′max

…….. (eq.9)

where H'max is ln (natural logarithm) of S (number of species).

Simpson's index of diversity was calculated as follow:

D = 1 − ∑ (pi)2si=1 …………………….. (eq.10)

where, D = Simpson's diversity index; pi=as described in equation 1

Simpson diversity index gives relatively little weight to the rare species and more weight

to the most abundant species [30]. The value ranges from 0 (low diversity) to a maximum of

(1-1/s), where S is the number of species. It is predominantly affected by sample size [30]:

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Simpson or dominance index (D) =-∑s [(Ni(Ni−1)]

i=1 N(N−1) ……………. (eq.11)

where, Ni is the number of individuals of speciesi; N is the total number of individuals of all

species. As index values increase, diversity decreases

3. 3. Important value index (IVI)

The importance value index (IVI) was calculated as follows to rank species contribution

to the forest community composition [29]:

IVI = RD + RF + RDO ……………………………………… (eq.12)

where, RD is relative dominance, RF s relative frequency, and RA is relative abundance.

RD = 𝑁𝑢𝑚𝑏𝑒𝑟𝑜𝑓𝑖𝑛𝑑𝑖𝑣𝑖𝑑𝑢𝑙𝑎𝑜𝑓𝑎𝑆𝑝𝑝

𝑇𝑜𝑡𝑎𝑙𝑛𝑢𝑚𝑏𝑒𝑟𝑜𝑓𝑖𝑛𝑑𝑖𝑣𝑖𝑑𝑢𝑎𝑙𝑜𝑓𝑆𝑝𝑝× 100 ……………………… (eq.13)

RF = 𝐹𝑟𝑒𝑞𝑢𝑒𝑛𝑐𝑦𝑜𝑓𝑎𝑆𝑝𝑝

𝐹𝑟𝑒𝑞𝑢𝑒𝑛𝑐𝑦𝑜𝑓𝑎𝑙𝑙𝑆𝑝𝑝× 100 …………………………………… (eq.14)

RDO = 𝐷𝑜𝑚𝑖𝑛𝑎𝑛𝑐𝑒𝑜𝑓𝑎𝑆𝑝𝑝

𝐷𝑜𝑚𝑖𝑛𝑎𝑛𝑐𝑒𝑜𝑓𝑎𝑙𝑙𝑆𝑝𝑝× 100 …………………………….… (eq.15)

Basal area (BA) (m2 ha-1) and volume (Vt) (m3 ha-1) for the natural forest was calculated

using inventoried data. Total volume was calculated using the conventional volume equation

because local volume equations not available for these species:

V =𝜋 (𝐷𝐵𝐻

4) 2 ∗ ℎ ∗ 𝑓 [24] ………………………………….….. (eq.17)

where V = tree volume, DBH= diameter at breast height, h = total height, 𝑓 = form factor (0.42)

[24].

BA (Basal area) calculated using the formula (eq.18):

BA = 𝜋𝐷𝐵𝐻2

4 …………………………………………… (eq.18)

where BA = Basal area, DBH = Diameter at breast height, 𝜋 = 3.142

3. 4. Regeneration status

Regeneration was analyzed based on the density of the seedlings, saplings, and stems

(matured individuals) ha-1 and categorized as :- (a), Good regeneration (GR) if the ratio of:-

“seedlings : saplings” and “saplings : stems‟ > 1 or seedlings >> saplings > mature individuals

(for shrub species if the ratio of seedlings : saplings (small trees)” > 1 or seedlings >> saplings)

: (b), Fair regeneration (FR) if the ratio of “seedling : sapling” ≥ 1 and/or “saplings: stem” ≥ or

≤ 1 or seedlings ≥ saplings ≥ or ≤ stem : (c), Poor regeneration (PR) if the ratio of “seedling :

sapling” < 1 and “sapling : stem” ≥ 1 or ≤ 1 or seedling < sapling ≥ or ≤ stem” : (d), No

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regeneration (NR) if a species is represented only by stem individuals and (e) New (N) if the

Species is represented only by seedling stage [31] and [10]. Further analysis of the regeneration

status of the species, forest patches, altitudinal gradient, and slope percent was made based on

these categories.

4. RESULTS

4. 1. Species composition and abundance of Chilimo forest

A total of 31 species of trees and shrubs, representing 25 families were recorded in all

study plots. Out of these, 20 (64.52 %) were trees and 11 (35.48 %) were shrubs. Sixteen

(51.61%) species were encountered in all forest patches, 6 (19.36 %) in two forest patches and

9 (29.03 %) in one forest patch. Thereof, 28, 23 and 26 species under highest, middle and lowest

altitudinal gradient were recorded. Moreover, 27, 29 and 25 species were recorded under gentle,

middle and steep slopes, respectively.

The total number of individuals in Chilimo forest patch was ranged from 2479.84 to19.05

N ha-1 for Podocarpus falcatus and Ilex mitis and 1919.55 to 19.05 N ha-1 for Maytenus

gracilipes and Rosa abyssinicus, in 2012 and 2017, respectively. The total number of

individuals in 2017 was ranged from 802.75 to 3.81 N ha-1 for Olea europea and Ilex mitis for

trees and 1854.6 to 3.81 N ha-1 for shrubs under the same forest patch. The number of

individuals trees sampled under Gallessa forest patch was ranged from 565.65 to28.31 N ha-1

for Juniperus procera and Ekebergia capensis and 263.49 to 29.85 N ha-1 for Juniperus procera

and Scolopia theifolia in 2012 and 2017, respectively and for Gaji forest patch in 2012 ranged

333.42 to 15.24 N ha-1 for Podocarpus falcatus and Buddleja polystacha and 297.47 to 3.81 for

Olea europea and the same species in 2012 and 2017, respectively. The number of individuals

for shrubs was also ranged from 1860.42 for Dovyalis abyssinicus to 50 N ha-1 for Osyris

quadripartita.

The 5 most abundant tree species under Chilimo forest patch was :- Podocarpus falcatus,

Olea europea, Allophyllus abyssinicus, Juniperus procera and Bersama abyssinicus, in

Gallessa were Juniperus procera, Allophyllus abyssinicus, Podocarpus falcatus, Bersama

abyssinicus and Scolopia theifolia and in Gaji:- Podocarpus falcatus, Olea europea, Allophyllus

abyssinicus, Juniperus procera and Scolopia theifolia. Moreover, the most abundant shrub

species under Chilimo forest patch were Maytenus gracilipes, Myrsine africana, Rhamnus

prenoides, Dovyalis abyssinicus and Carissa spinorrum in Gallessa Dovyalis abyssinicus,

Maytenus gracilipes and Maytenus addat and in Gaji were Dovyalis abyssinicus, Maytenus

gracilipes and Rhamnus prenoides.

4. 2. Species richness and diversity

Dendrometry and tree data measurements of diameter at breast height, diameter at stump

height and height were made for 2,379 trees. The most dominant tree species were: - Juniperus

procera, Podocarpus falcatus, Olea europea, Scolopia theifolia and Allophylus abyssinicus. In

contrast, Cassiopourea malosana, Carissa spinorram, Osyris quadripartita, Sideroxylon

oxycanthum and Erica arborea are rare species. The diameter at breast height (DBH) and

diameter at stump height (DSH) of the sampled species were ranged from 5 to 121.82 and 5 to

126.67 cm, respectively. Total height of the sampled trees was also ranged from 0.5 to 39.00m.

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The species richness was ranged from one to eleven, while, the Shannon Weiner diversity

index was ranged from 1 to 2.21 (Table 1). The highest species richness and diversity index

were found under middle altitudinal gradient, while, the lowest species richness and diversity

index were found under the highest altitudinal gradient.

Table 1. Shannon wiener and richness index of the sampled plots of Chilimo natural forest.

Plo

t

No

Pat

ch

Tra

nse

ct

Ric

hn

ess

20

17

Sh

ann

on

20

17

Plo

t N

o

Tra

nse

ct

Fo

rest

pat

ch

Ric

hn

ess

20

17

Sh

ann

on

20

17

01 Chilimo T1 4 0.59 18 T4 Chilimo 2 0.33

02 Chilimo T1 5 1.27 19 T4 Chilimo 8 1.99

03 Chilimo T1 8 1.70 20 T4 Chilimo 5 1.31

04 Chilimo T1 7 1.11 23 T2 Gallessa 1 0.00

05 Chilimo T1 8 1.43 24 T2 Gallessa 1 0.00

06 Chilimo T2 8 1.91 25 T2 Gallessa 9 1.99

07 Chilimo T2 8 1.79 26 T2 Gallessa 2 0.38

08 Chilimo T2 5 1.15 27 T3 Gallessa 0 0.00

09 Chilimo T2 7 1.74 28 T3 Gallessa 7 1.43

10 Chilimo T2 6 1.62 29 T3 Gallessa 5 1.44

11 Chilimo T2 7 1.75 30 T4 Gallessa 5 1.18

12 Chilimo T2 11 2.210 31 T4 Gallessa 8 1.53

13 Chilimo T2 5 1.14 32 T1 Gaji 9 1.86

14 Chilimo T3 1 0.00 33 T1 Gaji 10 1.92

15 Chilimo T3 4 1.27 34 T1 Gaji 9 1.91

16 Chilimo T3 6 1.54 35 T2 Gaji 7 1.53

17 Chilimo T3 7 1.47

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Table 2. Diameter distribution of most sampled tree and shrubs for the overall forest

in 2012 (area = 1.4 ha)

Patch Year

Sppdiameter distribution in Chilimo dryafro montane forest

No Local name Scientific

name

Diameter distribution (cm)

Sum

≤ 1

0

10

-20

20

-30

30

-40

40

-50

50

-60

60

-70

≥ 7

0

Overall 2012 1 Gatira habessha Juniperus

procera 54 52 36 32 11 10 10 4 209

Overall 2012 2 Berbersa Podocarpus

falcatus 129 24 4 4 - - 1 2 164

Overall 2012 3 Dalecho Olinia

rochetiana 41 54 16 5 2 2 1 - 121

Overall 2012 4 Ejerssa Olea

european 23 20 18 8 3 2 - 2 76

Overall 2012 5 Sarara Allophylus

abyssinicus 22 19 6 3 1 - - - 51

Overall 2012 6 Gaallee/Amotta Scolopia

theifolia 28 16 4 - - - - - 48

Overall 2012 7 Kertame Maytenus

gracilipes 32 2 - - 1 - - - 35

Overall 2012 8 Anfar Buddleja

polystacha 14 8 4 - - - - - 26

Overall 2012 9 Tatessa Rhus

glutinosa 3 12 6 - - 1 - - 22

Overall 2012 10 Kombolcha Maytenus

addat 9 9 - - - - - - 18

Overall 2012 11 Algae Celtis

africana 2 8 2 5 - - - - 17

Overall 2012 12 Gaachanfullaa Cassipourea

malosana 1 10 4 - - - - - 15

Overall 2012 13 Mieessa Ilex mitis 1 3 2 - - 1 1 2 10

Overall 2012 14 Sombo Ekebergia

capensis 5 1 - - 1 - - 1 8

Overall 2012 15 Watto Osyris

quadripartita 6 2 - - - - - - 8

Overall 2012 16 Tikure inchet Prunus

africana 2 4 1 - - - - 1 8

Overall 2012 17 Cheleleka Apodytes

dimidiata 3 3 - 1 - - - - 7

Overall 2012 18 Azamire Bersama

abyssinicus 3 2 - - - - - - 5

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Overall 2012 19 Asta Erica arborea 2 2 1 - - - - - 5

Overall 2012 20 Biitee Sideroxylon

oxycanthum 1 3 - - - - - - 4

Overall 2012 21 Ceeka Calpurina

aurea 3 - - - - - - - 3

Overall 2012 22 Barooddoo Myrica

salicifolia - 2 - 1 - - - - 3

Overall 2012 23 Kosso Hagenia

abyssinica - - - 1 - - - 1 2

Overall 2012 24 Cheleleka Apodytes

dimidiata 1 - - - - - - - 1

Overall 2012 25 Agam Carissa edulis 1 - - - - - - - 1

Total 386 256 104 60 19 16 13 13 867

4. 3. Population structure of Chilimo forest

The diameter distribution of the sampled trees under Chilimo forest in 2012 and 2017 is

presented in Table 3. The number of stems for Juniperus procera, Podocarpus falcatus, Olinia

rochetiana, Olea europea and Allophyllus abyssinicus was highest in 2012. However, Carissa

spinorrum followed by Apodytes dimidiate was the lowest (Table 2). Similarly, in 2017, the

highest number of stems were measured for Juniperus procera, Podocarpus falcatus, Olea

europea, Olinia rochetiana and Allophyllus abyssinicus (Table 3). The lowest number of

diameter measurement was made for Dovyalis abyssinicus, Carissa spinorrum and Hagenia

abyssinicus (Table 3). Graphical representation is presented for the most frequent tree species

in Figure 2a - 2n. Juniperus procera and Podocarpus falcatus had an inverted J shaped

distribution. Olea europea followed a normal distribution pattern, Allophyllus abyssinicus and

Scolopia theifolia were followed a similar fashion and showed a normal population pattern.

Table 3. Diameter distribution of most sampled tree and shrubs for the overall forest

in 2017 (area = 1.4 ha).

Patch Year No Local name Scientific name

Diameter class distribution (cm)

Sum

≤ 1

0

10

_20

20

-30

30

-40

40

-50

50

-60

60

-70

≥ 7

0

Overall 2017 1 Gatira habessha Juniperus

procera 50 58 22 31 12 12 9 4 198

Overall 2017 2 Berbersa Podocarpus

falcatus 144 38 2 2 1 - 2 1 190

Overall 2017 3 Ejerssa Olea european 23 19 19 8 3 2 - 2 76

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Overall 2017 4 Dalecho Olinia

rochetiana 21 34 10 5 1 1 3 - 75

Overall 2017 5 Sarara Allophylus

abyssinicus 20 19 6 3 1 - - - 49

Overall 2017 6 Gaallee/Amotta Scolopia

theifolia 23 18 3 - - - - - 44

Overall 2017 7 Kertame Maytenus

gracilipes 31 6 1 - 1 - - - 39

Overall 2017 8 Anfar Buddleja

polystacha 14 8 3 - - - - - 25

Overall 2017 9 Tatessa Rhus glutinosa 4 13 5 - - 1 - - 23

Overall 2017 10 Algae Celtis africana 2 6 6 3 - - - - 17

Overall 2017 11 Kombolcha Maytenus addat 10 7 - - - - - - 17

Overall 2017 12 Sombo Ekebergia

capensis 9 1 3 - - 1 - 1 15

Overall 2017 13 Gaachan fullaa Cassipourea

malosana 1 9 4 - - - - - 14

Overall 2017 14 Miessa Ilex mitis 1 2 2 1 2 1 1 2 12

Overall 2017 15 Watto Osyris

quadripartita 9 2 - - - - - - 11

Overall 2017 16 Tikure inchet Prunus africana 2 4 1 - - - - 1 8

Overall 2017 17 Cheleleka Apodytes

dimidiata 1 5 - 1 - - - - 7

Overall 2017 18 Azamire Bersama

abyssinicus 4 2 - - - - - - 6

Overall 2017 19 Biitee Sideroxylon

oxycanthum 2 3 - - - - - - 5

Overall 2017 20 Asta Erica arborea 2 1 1 - - - - - 4

Overall 2017 21 Barooddoo Myrica

salicifolia 0 4 - - - - - - 4

Overall 2017 22 Ceeka Calpurina aurea 3 0 - - - - - - 3

Overall 2017 23 Hetto Hagenia

abyssinica 0 0 - - - - - 1 1

Overall 2017 24 Agam Carissa edulis 1 0 - - - - - - 1

Overall 2017 25 Koshim Dovyalis

abyssinica 1 - - - - - - 1

Sum 377 260 88 54 21 18 15 12 845

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Figure 2a. Diameter distribution 2012 J. procera Figure 2b. Diameter distribution 2017 J. procera

Figure 2c. Diameter distribution 2012 P. falcatus Figure 2d. Diameter distribution 2017 P. falcatus

Figure 2e. Diameter distribution 2012 O. rochetiana Figure 2f. Diameter distribution 2017 O. rochetiana

54 52

3632

11 10 10

4

0

10

20

30

40

50

60

≤ 10 10_20 20 - 30 30 - 4040 - 50 50 - 60 60 - 70 ≥ 70

Nu

mb

er

of

ste

ms

Diameter class (cm)

Juniperus procera, 2012

50

58

22

31

12 12 94

0

10

20

30

40

50

60

70

≤ 10 10_20 20 -30

30 -40

40 -50

50 -60

60 -70

≥ 70

Nu

mb

er

of

ste

ms

Diameter class (cm)

Juniperus procera, 2017

129

24

4 4 0 0 1 20

20

40

60

80

100

120

140

≤ 10 10_20 20 -30

30 -40

40 -50

50 -60

60 -70

≥ 70

Nu

mb

er

of

ste

ms

Diameter class (cm)

Podocarpus falcatus, 2012

144

38

2 2 1 0 2 10

20

40

60

80

100

120

140

160N

um

be

r o

f st

em

s

Diameter class (cm)

Podocarpus falcatus, 2017

41

54

16

52 2 1 0

0

10

20

30

40

50

60

≤ 10 10_20 20 -30

30 -40

40 -50

50 -60

60 -70

≥ 70

Nu

mb

er

of

ste

ms

Diameter class (cm)

Olinia rochetiana, 2012

21

34

10

51 1

30

0

5

10

15

20

25

30

35

40

Nu

mb

er

of

ste

ms

Diameter class (cm)

Olinia rochetiana, 2017

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Figure 2g: Diameter distribution 2012 A. abyssinicus Figure 2h. DBH distribution 2017 A. abyssinicus

Figure 2i. Diameter distribution 2012 O. europea Figure 2j. Diameter distribution 2017 O. europea

Figure 2k. Diameter distribution 2012 S. theifolia Figure 2l. Diameter distribution 2017 S .theifolia

22

19

6

31 0 0 0

0

5

10

15

20

25

Nu

mb

er

of

ste

ms

Diameter class (cm)

Allophyllus abyssinicus, 2012

20 19

6

31 0 0 0

0

5

10

15

20

25

Nu

mb

er

of

ste

ms

Diameter class (cm)

Allophyllus abyssinicus, 2017

2320

18

8

3 20

2

0

5

10

15

20

25

Nu

mb

er

of

ste

ms

Diameter class (cm)

Olea europea, 2012

23

19 19

8

3 20

2

0

5

10

15

20

25

Nu

mb

er

of

ste

ms

Diameter class (cm)

Olea europea, 2017

28

16

4

0 0 0 0 00

5

10

15

20

25

30

Nu

mb

er

of

ste

ms

Diameter class (cm)

Scolopia theifolia, 2012

28

18

3

0 0 0 0 00

5

10

15

20

25

30

≤ 10 10_20 20 -30

30 -40

40 -50

50 -60

60 -70

≥ 70

Nu

mb

er

of

ste

ms

Diameter class (cm)

Scolopia theifolia, 2017

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Figure 2m. Diameter distribution 2012 R. glutinosa Figure 2n. Diameter distribution 2017 R. glutinosa

4. 4. Frequency, density, dominance and important values index of Chilimo dry

Afromontane forest

The relative (frequency, density, dominance and IVI) for 2012 and 2017 of the studied

natural forest is presented in Table 4. In 2012, the relative frequency was ranged from 18.01

(Juniperus procera) to 0.25 (Allophyllus abyssinicus). Juniperus procera, Podocarpus falcatus,

Olinia rochetiana, Rhus glutinosa and Maytenus gracilipes were most frequent tree species, on

the contrary, Carissa spinorrum and Calpuria aurea were less frequent species. The relative

density in 2012 also ranged from 17.65 for Juniperus procera to 0.31 N ha-1 for Carissa

spinorrum. The relative dominance ranged from 45.55 to 0.01 G ha-1 for Juniperus procera and

Carissa spinorram. The IVI in 2012 ranged from 27.14 (Juniperus procera) to 0.22 (Carissa

spinorrum). The relative frequency in 2017 ranged from 13.24 for Juniperus procera to 0.46

for Sideroxylon oxycanthum. The relative density also ranged from 23.55 to 0.12 % for Carissa

spinorrum and Hagenia abyssinica (Table 4). The relative dominance also ranged from 44.98

for Juniperus procera to 0.01 G m2 ha-1 for Carissa spinorrum.

Table 4. Relative (frequency, density,dominance) and IVI for Chilimo dry afromontane

forest DBH ≥ 5 cm

Species Habit

2012 2017

RF

(%) RD (%)

RDO

(%)

IVI

(%) RF %

RD

(%)

RDO

(%)

IVI

(%)

Juniperus procera Tree 18.01 24.61 45.55 27.14 13.24 23.55 44.98 26.51

Olinia rochetiana Tree 11.41 10.38 8.57 10.17 11.41 9.46 8.51 9.90

2

8

2

5

0 0 0 00

1

2

3

4

5

6

7

8

9

≤ 10 10_20 20 - 3030 - 4040 - 5050 - 6060 - 70 ≥ 70

Nu

mb

er

of

ste

ms

Diameter class (cm)

Rhus glutinosa, 2012

4

13

5

0 01

0 00

2

4

6

8

10

12

14

Nu

mb

er

of

ste

ms

Diameter class (cm)

Rhus glutinosa, 2017

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Podocarpus falcatus Tree 11.41 19.54 8.01 12.62 11.41 22.36 8.42 13.77

Olea europea Tree 10.05 9.16 12.36 10.56 10.05 9.11 12.68 10.61

Maytenus gracilipes Shrub 8.22 4.10 0.80 4.60 8.22 4.14 0.95 4.66

Buddleja polystacha Tree 5.94 3.14 1.13 3.55 5.94 3.19 1.13 3.56

Rhus glutinosa Tree 5.02 2.78 1.99 3.38 5.02 2.76 1.98 3.35

Scolopia theifolia Tree 5.02 5.79 1.65 4.14 5.02 5.21 1.51 3.95

Maytenus addat Shrub 3.20 2.18 0.61 2.05 3.20 2.25 0.55 2.06

Osyris quadripartita Shrub 3.20 0.96 0.15 1.55 3.20 1.30 0.20 1.66

Ekebergia capensis Tree 3.65 0.96 2.27 2.42 3.65 1.42 2.32 2.55

Cassiopourea

malosana Tree 2.28 1.69 0.96 1.68 2.28 1.65 1.00 1.69

Apodytes dimidiata Tree 1.82 0.85 0.39 1.07 1.82 0.83 0.45 1.09

Bersama abyssinicus Tree 1.82 0.60 0.09 0.90 1.82 0.59 0.10 0.90

Erica arborea Tree 1.37 0.60 0.19 0.76 1.37 0.47 0.16 0.71

Ilex mitis Tree 1.37 1.45 5.33 2.70 1.37 1.42 5.37 2.67

Myrica salicifolia Tree 1.37 0.49 0.18 0.73 1.37 0.47 0.22 0.73

Prunus africana Tree 1.37 0.96 2.16 1.51 1.37 0.95 2.22 1.52

Calpuria aurea Shrub 0.92 0.36 0.04 0.47 0.92 0.35 0.05 0.46

Celtis africana Tree 0.92 2.41 2.41 1.84 0.92 2.13 2.45 1.77

Carissa spinorram Shrub 0.46 0.13 0.01 0.22 0.46 0.12 0.01 0.21

Hagenia abyssinica Tree 0.46 0.24 1.57 0.76 0.46 0.12 1.31 0.63

Sideroxylon

oxycanthum Tree 0.46 0.49 0.17 0.37 0.46 0.47 0.18 0.39

Allophylus abyssinicus Tree 0.25 6.15 3.41 4.82 5.02 5.68 3.25 4.65

Sum 100 100 100 100 100 100 100 100

where: RF; Relative frequency: relative Density, RDO: relative dominance: IVI; Important

value index

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4. 5. Above-ground carbon, basal area, and number of stems

Figure 3a-d. Basal area (m2 ha-1) and number of stems (N ha-1) 2012 vs 2017 along alt

gradient, slope, forest patch and land use type

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Figure 3e-h. Number of stems (N ha-1) 2012 vs 2017 along alt gradient, slope, forest patch

and land use type

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The aboveground biomass for the sampled species in 2012 was ranged from 184.62 to

0.23 t C ha-1 for Juniperus procera and Carissa spinnorrum, respectively (Table 4). The basal

area was ranged from 16.15 to 0.06 m2 ha-1 in 2017 (Table 4). The number of stems was ranged

from 250 to 25. The highest number of stems was recorded for Juniperus procera followed by

Celtis africana. While, the lowest number of stems 25 N ha-1 was recorded for Ekebergia

capensis (Table 4).

The basal area and number of stems in the studied forest was significantly varied among

species, forest type and time of measurements. The basal area increased along with an increase

in time and ranged from 25 to 0.36 m2 ha-1 and 29.52 to 0.29 m2 ha-1 in 2012 and 2017,

respectively (Table 4). The 5 thickest trees were: - Juniperus procera, Ilex mitis, Olea europea,

Podocarpus falcatus, Olinia rochetiana and Rhus glutinosa. However, the thinnest trees were:

- Ekebergia capensis, Bersama abyssinicus, Osyris quadripartita and Mayrica salicifolia

(Table, 3). The basal area of Allophyllus abyssinicus, Celtis africana, Ekebergia capensis,

Juniperus procera, Maytenus addat, Olinia rochetiana and Rhus glutinosa decreased along

with increasing in time. On the contrary, the basal area of Apodytes dimidiata, Cassiopourea

malosana, Ilex mitis, Osyris quadripartita, Prunus Africana and Scolopia theifolia also

increased along with increasing in time. More trees belonging to a lower diameter class (Table

3). In addition, larger diameter class at breast height (DBH), low species diversity and density

recorded under higher altitudinal gradients (Figures 4(A,B), 5(A,B). The number of stems

ranged from 475 to 25. The highest number of stems recorded for Juniperus procera followed

by Celtis africana. While, the lowest number of stems 25 N ha-1 recorded for Ekebergia

capensis, Erica arborea and Myrica salicifolia.

4. 6. Growth and yield of eleven selected tree species of Chilimo natural forest

The height, diameter, basal area and volume of the sampled trees is presented in Table 5.

The ANOVA revealed that diameter, height, basal area and volume was significantly varied

among the species at P ≤ 0.05 (Table 6). The total height of the sampled trees varied among the

species. Juniperus procera had the highest height growth followed by Prunus africana.

However, Scolopia theifolia had the lowest height growth. The highest diameter growth

recorded for Juniperus procera followed by Olea europea. The mean annual volume and basal

area increment ranged from 0.330 to 2.338 m3 ha-1yr-1 and 0.007 to 0.47 m2 ha-1 yr-1. The mean

annual volume increment was highest for Podocarpus falcatus and lowest for Ekebergia

capensis. The mean annual diameter increment was highest for Juniperus procera and lowest

for Ruth glutinosa. In addition, the mean annual volume and basal area increment was highest

for Juniperus procera followed by Olea europea. However, the lowest mean annual, volume

and basal area increment observed for Ruth glutinosa followed by Scolopia theifolia.

Table 5. Analysis of variance for growth parameters.

Parameters Factor DF SS MS F - Value Pr> F

Volume 2012

Volume 2017

BA2012

BA2017

Species

Species

Species

Species

10

10

10

10

67.2

81

0.483

0.531

6.720

8.101

0.048

0.053

3.93

6.352

5.47

5.80

3.31e-05***

6.47e-06***

8.2e-08***

2.2e-08***

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Ht2012

Ht2017

Dbh2012

Dbh2017

HtI

DbhI

VtI

BAI

Annual DBHI

Annual HtI

Annual VtI

Annual BAI

Species

Species

Species

Species

Species

Species

Species

Species

Species

Species

Species

Species

10

10

10

10

10

10

10

10

10

10

10

10

7514

6830

26484

25614

95.8

102.5

0.710

0.0014

4.10

3.83

0.028

0.00006

751.4

683.0

2648.4

2561.4

9.581

10.249

0.07

1.42e-04

0.41

0.383

0.003

5.67e-06

14.73

14.67

11.54

11.45

3.35

7.458

7.70

7.77

7.46

3.35

7.70

7.77

2e-16***

<2e-16***

<2e-16***

<2e-16***

0.000288***

2.89e-11***

1.1e-11***

8.43e - 12***

2.89e - 11***

0.000288***

1.1e - 11***

8.43e - 12***

where: Ht: total height, Dbh: diameter at breast height, Vt; volume increment, BA; basal area

and I; increment, *** ; Highly significant at P < 0.01

Table 6. Mean ± standard deviation of the different growth parameters for eleven native

tree species.

Species

Mean Dbh

(cm)

Mean height

(m)

No

(N ha-1)

Basal area

(m2 ha-1)

Volume

(m3 ha-1)

2012 2017 2012 2017 2012 2017 2012 2017 2012 2017

Allophyllus abyssinicus 13.88 14.99 12.11 13.70 106.82 106.82 2.50 2.57 16.85 19.97

Apodytes dimidiata 13.44 15.47 12.48 15.11 43.75 43.75 0.839 0.997 5.761 7.199

Celtis africana 21.6 22.79 15.66 16.90 105 105 9.804 10.715 70.47 82.16

Ekebergia capensis 22.79 23.93 10.5 12.02 40 40 3.899 4.010 34.90 36.55

Juniperus procera 24.59 26.23 16.71 18.69 179.81 179.81 14.06 15.10 157.85 178.02

Olea europea 21.35 22.21 15.44 16.76 88.10 88.10 4.80 5.27 50.22 54.50

Olinia rochetiana 16.77 17.84 14.76 16.1 82.29 82.29 2.89 3.10 28.87 31.87

Prunus africana 26.50 27.98 18.72 20.82 43.75 43.75 0.662 0.695 9.031 9.688

Podocarpus falcatus 8.74 10.68 8.38 10.54 167.39 167.39 2.68 3.10 30.192 34.22

Rhus glutinosa 16.82 17.51 12.77 13.89 50 50 1.48 1.58 9.53 10.61

Scolopia theifolia 9.72 11.05 9.05 11.42 110 110 1.108 1.321 6.377 8.396

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Table 6(continue). Mean ± standard deviation of the different growth parameters

for eleven native tree species.

Species

Average

Diameter

increment

(cm)/yr-1

Average

Height

(m)/ yr-1

Vincrement

(m3ha-1yr-1)

G increment

(m2ha-1yr-1)

Vincrement

(m3tree yr)

BA increment

(m2 tree year)

Allophyllus abyssinicus 0.22 0.32 0.624 0.014 0.0058 0.0005

Apodytes dimidiata 0.405 0.525 0.288 0.0316 0.0066 0.00072

Celtis africana 0.238 0.248 2.338 0.182 0.0104 0.00081

Ekebergia capensis 0.228 0.3045 0.330 0.0222 0.0083 0.0006

Juniperus procera 0.33 0.40 4.034 0.21 0.02 0.0012

Olea europea 0.172 0.264 0.856 0.47 0.0092 0.0006

Olinia rochetiana 0.22 0.27 0.60 0.042 0.0073 0.0005

Prunus africana 0.296 0.418 0.131 0.0066 0.0209 0.0011

Podocarpus falcatus 0.38 0.43 0.81 0.084 0.0048 0.0005

Rhus glutinosa 0.138 0.224 0.216 0.02 0.0043 0.00037

Scolopia theifolia 0.266 0.474 0.404 0.043 0.0037 0.00039

where: Dbh; Diameter at breast height, N: number of stems, ha; hectare,

4. 7. Growth and yield along an altitudinal gradient

Diameter growth of the sampled trees under 3 altitudinal gradient ranged from 5 to 121.5

cm and non significant. Highest diameter growth recorded among the highest altitudinal

gradient, however, the lowest recorded under middle altitudinal gradients. The highest mean

weighted height increment also observed in the highest altitudinal gradient, however, the lowest

was observed in the middle altitudinal gradients.

The weighted mean diameter increment also showed a decreasing trend along with

increasing in altitudinal gradient. The mean annual diameter and height increment also highest

in the lower altitudinal gradient. The mean annual volume increment was showed a decreasing

trend along with increasing in altitudinal gradients.

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(A)

(B)

Figure 5(A,B). Diameter and height growth for the sampled trees along altitudinal

gradient in 2017

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(A)

(B)

Figure 6(A,B). Basal area and volume increment per tree per year along altitudinal gradient

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4. 8. The status of saplings, seedlings and shrubs synopsis

The shrubs, saplings and seedlings distribution under Chilimo dry Afromontane forest is

presented in Table 6. The 5 most commonly recorded shrub species were: - Myrsine africana,

Maytenus gracilipes, Dovyalis abyssinica, Carissa spinorrum and Osyris quadripartita. The

number of shrubs ranged from 1150.5 to 3.81 N ha-1 for Myrsine africana and Calpurea aurea,

respectively. The number of stems for Maytenus gracilipes, Dovyalis abyssinicus and Osyris

quadripartite decreased in 2017, while, Myrisen africana, Carissa spinorrum, Rosa abyssinicus

and Gnidia glauca remained constant. The number of stems for saplings ranged from 1230.48

for Podocarpus falcatus to 3.8 N ha-1 for Erica arborea. Podocarpus falcatus, Juniperus

procera, Scolopia theifolia, Bersama abyssinicus and Olea europea had good number of

saplings. While, Allophyllus abyssinicus and Olinia rochetiana had lower number of saplings

(Table 6). A total of 20 species of seedlings recorded into 2 measurement periods. Their number

ranged from 4059.70 to 119.40 N ha-1. In 2012, 3 species had good, 2 fair, 16 poor and 12 no

regeneration. Similarly, in 2012 10 had fair, 5 poor and 14 no regeneration. In 2017, 2 had good,

5 fair, 2 poor, 4new and 16 no regeneration. Allophyllus abyssinicus, Buddleja polystacha,

Cassiopourea malosana, Celtis africana had good regeneration.

4. 9. Seedlings, saplings, and shrubs of native tree species along altitudinal gradient and

slope

The ANOVA for saplings, seedlings and shrubs significantly varied among altitudinal

gradient and slope at P < 0.05. In 2012, the number of saplings for Podocarpus falcatus,

Bersama abyssinicus and Scolopia theifolia were better than others. Podocarpus falcatus and

Juniperus procera under lower and middle altitude, Ekebergia capensis under lower altitude

and Scolopia theifolia and Bersama abyssinicus under middle altitude had good number of

saplings. On the contrary, Rhus glutinosa, Prunus africana and Buddleja polystacha had very

poor number of saplings.

Among the 26 species under lower altitude, 1had fair, 10 poor, 6 new and 9 no

regeneration. In middle altitude, 1 good, 3 fair, 6 poor, 5 new - and 7 no regeneration and in

highest altitude, 5 fair, seven poor, 7 new and 9 no regeneration. Podocarpus falcatus under

lower and upper altitude had good regeneration, Allophyllus abyssinicus, Olea europea and

Scolopia theifolia under lower, middle and higher altitude had fair regeneration. Cassiopourea

malosana, Ekebergia capensis, Olinia rochetiana, Rhus glutinosa and Scolopia theifolia had

poor regeneration. Olea europea under lower, Allophyllus abyssinicus middle and Prunus

africana, Dombeya torrida and Sideroxylon oxycanthum highest altitudes had new

regeneration. On the contrary, Apodytes dimidiata, Buddleja polystacha, Prunus africana under

lower, Juniperus procera (2017), Erica arborea, Hagenia abyssinica highest altitude had no

regeneratiuon.

5. DISCUSSION

5. 1. Species composition, structure and regeneration status of the forest

The present study is investigated the species composition, diversity, growth and

regeneration status of Chilimo dry Afromontane forest along an altitudinal gradient, slope and

species. The total number of tree and shrub species (31) recorded in this study are more or less

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in line with the reports of [32] and [10]. However, the number of species recorded under

Chilimo dry afromontane forest is lower than (Kumto dry afromontane forest [33]; Berbere

forest [34] , (170 species), Denkoro forest (174 plant species [35], Dodola forest (113 plant

species [36], Belete forest (157 plant species) [37] and Kimphelafa forest (130 plant species)

[38], Mana Angeto forest (211 plant species [39], Bale mountain national park forest (230 plant

species) [40] and Nechisar national park forest (208 plant species [41], Achera forest (48 woody

species) [42]and Boda dry afromontane forest (95 species) [43], Kumuli dry afromontane forest

(133 woody species) [44] and Tara Gedam dry afromontane forest (143 woody species) [45].

The most dominant trees under Chilimo dry Afromontane forest are: - Juniperus procera,

Podocarpus falcatus, Olea europea, Scolopia theifolia and Allophyllus abyssinicus. In contrast,

Cassiopourea malosana, Carissa spinorrum, Osyris quadripartita, Sideroxylon oxycanthum

and Erica arborea are rare species. Podocarpus falcatus in Chilimo, Juniperus procera in

Gallessa and Gaji are dominant species. Similarly, [10] reported Juniperus procera in Gallessa

and Chilimo and Olea europea in Gaji as dominant species. Hagenia abyssinica and Dombeya

torrida in Gallessa; Ilex mitis in Chilimo are rare species [32]. In the current study, Hagenia

abyssinica is found to be rare and no regeneration, but, Buddleja polystacha and Ilex mitis are

showed some improvements.

The higher tree species diversity and richness in the middle elevation gradients might be

due to better microclimate condition and favorable temperature. The lower biomass, diversity

and dominance in the lower and higher altitudinal gradient is also related to anthropogenic

disturbance. In line with, similar reports is also reported by [10, 15, 46] and [47]. In addition,

[33] found high species diversity in the middle altitudinal gradient in Kumto dry Afromontane

moist forest of Eastern Wellega zone, West Ethiopia. The differences in species richness arises

from altitudinal differences, climatic conditions and anthropogenic effect. But, the diversity

index of Chilimo forest is higher than Boda forest with the overall, diversity and evenessof 1.79

and 0.09 [43].

The tree density and basal area of Chilimo forest is lower than other tropical forests (685

- 820 tree ha-1) and (18.9 to 19.58 m2 ha-1), tropical semi - evergreen forest (34 to 610

individuals ha-1) and (7.81 to 98.58 m2 ha-1) tropical wet evergreen forest [48]. The Shannon

diversity index of this study is 0.5 to 2.21 in line with 1.5 to 3.5 recommended by [49] but lower

than tropical semi evergeen forest of Mizoran [50] Achera forest ( H’ was 3.37) [42].

The diameter distribution of Chilimo forest is found to be an inverted J shaped

distribution. This is might be due to a big number of stems shrubs, small sized tree species and

younger individuals of big sized tree species, too. Regarding the forest profiles few tree species

in the tree layer has contributed to most of the total dbh of Chilimo forest. These are Juniperus

procera, Olinia rochetiana, Podocarpus falcatus, Olea europea and Maytenus gracilipes

(65.45 %). Similar results are also reported by Shambel Bantiwalo (51). According

toLamprecht [23] the normal basal area of virgin tropical forest in Africa is 23 - 37 m2 ha-1.

Tree height value is also higher in the lower class and decreased in the higher class.This is also

true for other forests too [42].

This revealed that the forest is also suffered from selective cutting, this result smaller to

medium sized individuals attributed to high rate of regeneration but low recruitment. Similar,

results are also reported in Koto forest [33]. The DBH distribution of Chilimo forest is in line

with Tara Gedam dry Afromontane forest [45], Kumli forest [44], Indian forest [52], forest of

North East India [53] and [54]. The reverse J - shaped population curve of trees suggests an

evolving or expanding population, climax or stable type of population in forest ecosystems

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indicating that the forest harbors a growing and healthy population [58], [56] and [59]

(Parthasarathy and Karthikeyan 1997; Mishra et al. 2005; Sahu et al. 2012). Among the most

dominant tree, species Juniperus procera and Podocapus falcatus showed an inverted J shaped

distribution, Juniperus procera represented in all the diameter class, while, Podocarpus

falcatus, in lower diameter class. Similar results are also reported by [43] for Boda forest of

western Shewa, but Chilimo forest has lower basal area than Boda forest 114.64 m2·ha-1

reported by [43]. The lower value of IVI of the Chilimo forest indicating that majority of species

are rare species. This attributed to different density dependent and density independent factors

such as competition for nutrients, poor seed dispersal and germination.

The regeneration potential of the species under Chilimo dry Afromontane forest varied

along altitudinal gradient, slope and species. This is might be due to differences in climatic

condition and disturbance level. Podocarpus falcatus had good regeneration potential under

lower altitude, while, Juniperus procera under highest altitude. Hagenia abyssinica and

Apodytes dimidiata represented by few individuals. In addition, among the endemic species

Rhus glutinosa is a threatened and vulnerable species as mentioned by [9] and [10]. Rhus

glutinosa showed a U shaped distribution pattern due to lack of trees in the upper and lower

diameter classes.

Podocarpus is represented by more number of seedlings an indicative of excellent

recruitment which also reflects the prevailing environmental conditions. This entails high biotic

potential of the species which may be supported by existing environmental conditions. Similar

trends are also reported for Gedho dry Afromontane forest of West Shewa zone [57] and Tara

Gedam forest at South Gondar Zone, NW Ethiopia [45]. Trees and saplings densities varied

significantly among species, Podocarpus, showed the highest tree and sapling density.

Podocarpus is also the dominant tree species in dry Afromontane forest in Ethiopia [6]. The

population density of Podocapus falcatus in Chilimo is higher than Herenna forest [58] and

Dindin [59] Wef - Washa [60] and Menagesha - Suba state forest [61].

In 2017, the number of saplings for Podocarpus falcatus, Juniperus procera, Scolopia

theifolia, Bersama abyssinicus, Olea africana, Allophyllus abyssinicus and Olinia rochetiana

decreased, due to higher disturbance. While, the number of saplings for Ilex mitis, Cassiopourea

malosana, Prunus africana, Sideroxylon oxycanthum and Erica arborea remained constant.

Among the thirty - one sampled species in 2012 (38.70 %) 45.11 % in 2012 no regeneration, so

these species either they produce non - viable seeds or there might be some problems of

regeneration.

The differences in density of seedlings and saplings among the three forest patches might

be due to difference in biotic and abiotic factors [62], i.e. variation in site conditions,

disturbance level, species colonization and ecological properties [63] and [31]. Maytenus

gracilipes, Olea europaea, Podocarpus falcatus, Scolopia theifolia, Allophyllus abyssinicus

and Bersama abyssinica are among shade - tolerant species [32] and [9]. Seventeen % of the

tree species had no regeneration, this is might be due to high anthropogenic disturbance, animal

trampling and poor biotic potential of tree species.

Moreover, 7 species contributing 22.58 % of tree species where new arrivals are very

poor and have been felled by locals but seed remains as seed - bank and germinate during the

favorable season. The ratio of the seedling to mature individuals is 2.85 : 1, the ratio of the

seedling to saplings is 16.04 : 1 and saplings to mature individuals is 0.35 : 1. Juniperus procera,

Olinia rochetiana, Podocarpus falcatus, Olea europea and Maytenus gracilipes (65.45 %) have

contributed to major portion of the total dbh of Chilimo forest. Juniperus had individuals almost

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in most dbh classes indicating both good regeneration and good recruitments. While, Apodytes

dimidiata, Juniperus procera and Olinia rochetiana had poor regeneration and good

recruitment. Prunus africana indicating both poor regeneration and poor recruitments.

The data analysis revealed that the density value for seedling and saplings of the

population structure of the forest are high compared to the structure of individuals and agrees

with the normal patterns of the population. This implies the need to develop and implement

forest management regimes in the area in order to promote healthy regeneration. The less

number of sapling individuals as compared to seedlings implying the death of most of the

seedlings before reaching the sapling stage due to human intervention, browsers, grazers and

nature of the seeds. [64] reported that seedling recruitment is a block in the population dynamics

of many species of trees.

It is one of the most important factors in determining the local abundance of adult trees

and this calls for an urgent conservation strategy. Hence, those species that don’t have seedling

and sapling and species represented by only seedlings are grouped under priority class I. Others

whose seedling density is between 1 and 10 are categorized under class II and the remaining

species under class III. The species under priority class I should get the first priority due to lack

of seedlings and then followed by class II that are represented by a few seedling individuals.

Subsequently, for the sake of conservation endeavors, the third group is also recommended to

be given the appropriate conservation priority.

5. 2. Growth and yield of the most common native tree species

The mean annual volume increment of Chilimo forest is better than reported for dry

evergreen Afromontane forest for lowland and dry forest estimated to 1m3 ha-1 yr-1 and volume

of about 100 m3 ha-1 [65] and [66]. Moreover, mean annual increment of Chilimo forest is also

higher than Acacia- Commiphora woodland (0.0015 m3ha-1yr-1) with the standing volume of

about 6.5 m3·ha-1 and desert and semi-desert scrub and evergeen scrubs [66]. The number of

stems for Chilimo forest reduced due to selective cutting is also true for other evergreen

Afromontane forests too [66-68]. The mean annual increment of Celtis africana and Olea

europea in the present study is 2.34 and 1.013 m3 ha-1 yr-1 is in line with the mean annual volume

increment of the native tree species under natural forest [69], [70] and [71]. The mean annual

volume increment of Chilimo forest is in line with other dry Afromontane forests found in

Ethiopia in different locations [72] and [73].

The low MAI for the other species is might be due to lower number of stocks as a result

of illegal logging [23] and [74]. Our results are also in line with the reports of other dry

Afromontane forest of North Western Ethiopia by Sisay et al.( 73) reported a volume increment

rate of 3.5 m3 ha-1 (Gelawdiwos dry Afromontane forest), 3.6 m3 ha-1 (Katassi dry Afromontane

forest) and 1.0 m3 ha-1 (Taragedam dry Afromontane forest) with volume growth.

Thus, the research finding is very important for sustainable management of the species.

Consider as a remediation measure to reduce illegal cutting and pressure on Chilimo dry

Afromontane forest, the mean annual increment of Juniperus procera in Chilimo area is also

found to be 4.223 m3 ha-1 yr-1 in line with the reports 0.5 to 5.65 m3ha-1 yr-1 for high forests

[70]. In general, the number of forest growth models for tropical rain forests is few due to the

complexity of these forests. While, such systems are common in many parts of the world [5].

Moreover, Ethiopia has no standardized forest inventory system in place and increment

rates of the limited remaining system areas available. This makes sustainable forest

management and harvesting difficult or even impossible.

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6. CONCLUSIONS

A total of 31 trees and shrubs representing 25 families were recorded, 20 (64.52 %) were

trees and 11 (35.48 %) were shrubs. There of 28, 23 and 26 species under highest, middle and

lowest altitudinal gradient were recorded.The most dominant tree species were: - Juniperus

procera, Podocarpus falcatus, Olea europea, Scolopia theifolia and Allophyllus abyssinicus.

The species composition, diversity, abundance, dominance and important value index

significantly varied among species, altitudinal gradient and slope. The diameter distribution

was an inverted J - shaped distribution pattern. The highest species richness and diversity index

were found under middle altitudinal gradient, while, the lowest species richness and diversity

index were found under the highest altitudinal gradient. Juniperus procera and Podocarpus

falcatus had an inverted J shaped distribution while Allophyllus abyssinicus and Scolopia

theifolia had U shaped population distribution pattern. The aboveground biomass was ranged

from184.62 to 0.23 t C ha-1 while the basal area was ranged from 16.15 to 0.06 m2 ha-1 and the

number of stems was ranged from 250 to 25. The structure and regeneration status of Chilimo

forest was deteriorated within the last 9 years. The MAI of the forest was ranged from 4.22 to

0.23 m3 ha-1yr-1 and the basal area increment was ranged from 0.85 to 0.020 m2 ha-1yr-1. In 2012,

3 had good, 2 fair, 16 poor and 12 no regeneration, while, in 2017, 10 species had fair, 5 poor

and 14 no regeneration. Allophyllus abyssinicus, Buddleja polystacha, Cassiopourea malosana,

Celtis africana had good regeneration, while, Hagenia abyssinica had no regeneration. There

is no forest management in the study forest either to increase productivity or yield, thus,

attention should be given in these regards. Awareness creation and training should be also given

for local people and integration of their indigenous knowledge to manage the forest. I suggest

implementation of sustainable forest management practices.

ACKNOWLEDGEMENTS

The authors' thanks Genene Tesfaye, Central Ethiopia Environment and Forest Research Centre, for assisting us

in field data collection and preparation of plant and soil samples, Mossissa Kebede from Oromiya Forest and

Wildlife Enterprise. The Swiss Government Excellent Scholarship programme is also highly acknowledged for

funding Mehari A. Tesfaye's fellowship and the Ethiopian Environment and Forest Research Institute (EEFRI),

headquarter, for covering the cost of fieldwork and laboratory analysis.

BIOGRAPHY

Mehari Alebachew Tesfaye born on 14 March 1978, Gojjam (Dangila), Ethiopia working as a senior researcher in

Ethiopian Environment and Forest Research Institute, Addis Ababa from 2002 to present. He awarded his Post

Doc International Forestry and Climate Change Bern University of Applided, Switzerlands (2018), PhD degree in

Sustainable Utilization and Conservation of Forest system, University of Valladolid, Spain (2015), MSC degree

in Environmnetal science, Addis Ababa University (2006), BSC degree in Forestry from Alemaya University

(1997). He published more 30 articles in local, regional and international peer reviwed journals.

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