Journal of Threatened
Taxa | www.threatenedtaxa.org | 26 February 2022 | 14(2): 20539–20549
ISSN 0974-7907
(Online) | ISSN 0974-7893 (Print)
https://doi.org/10.11609/jott.6786.14.2.20539-20549
#6786 | Received 07
October 2020 | Final received 13 September 2021 | Finally accepted 24 January
2022
Distribution, diet, and trophic
level of Arvicanthis abyssinicus
and Tachyoryctes splendens
around the area of recently extinct Ethiopian Wolf Canis
simiensis on Mount Guna,
northwestern Ethiopia
Hirpasa Teressa 1, Wondimu Ersino 2 & Tadele Alemayo 3
1 College of Natural and
Computational Sciences, Department of Biology, Wolkite
University, P.O. Box 07, Ethiopia.
2 Department of Biology, Wachemo University, HV3M+368, Hosaena,
Ethiopia.
3 Department of Wildlife and
Ecotourism Management, Mekelle University, Mekelle, Ethiopia.
1 hirpaifet100@gmail.com
(corresponding author), 2 wondimuersino5@gmail.com, 3 tadelealemayo@gmail.com
Editor: Giovanni Amori,
CNR - Institute of Research on Terrestrial Ecosystems, Roma, Italy. Date
of publication: 26 February 2022 (online & print)
Citation: Teressa, H., W. Ersino & T. Alemayo (2022). Distribution, diet, and trophic
level of Arvicanthis abyssinicus
and Tachyoryctes splendens
around the area of recently extinct Ethiopian Wolf Canis
simiensis on Mount Guna,
northwestern Ethiopia. Journal of Threatened Taxa 14(2): 20539–20549. https://doi.org/10.11609/jott.6786.14.2.20539-20549
Copyright: © Teressa et al. 2022. Creative Commons Attribution
4.0 International License. JoTT allows unrestricted use, reproduction, and
distribution of this article in any medium by providing adequate credit to the
author(s) and the source of publication.
Funding: Debre Tabor
University.
Competing interests: The authors
declare no competing interests.
Author details: Hirpasa Teressa is lecturer at Wolkite University, Department of Biology. He received a
bachelor’s degree in Applied Biology from Hawassa University and a master’s
degree in zoology from Mekelle University, Ethiopia. For the last 10 years, he
has been teaching different zoological courses, and conducting various
researches on animal ecology and conservation as well as on importance of
animal kingdom. Wondimu Ersino, a former lecturer at Wachamo University, is PhD students at Department of
Evolutionary Zoology and Human Biology, University of Debrecen, Hungary. He
received bachelor’s degree in Applied Biology from Ambo University and master’s
degree in Zoology from Mekelle University, Ethiopia. For the last 10 years, he
has thought different zoological courses, and conducted researches on Animal
Ecology. Tadele Alemayo, a former lecturer at
Department of Wildlife and Ecotourism Management, is PhD students at Mekelle
University, Ethiopia. He received bachelor’s degree in Applied Biology from
Mekelle University and master’s degree in Ecological and Systematic Zoology
from Jima University, Ethiopia.
Author contributions: All authors equally contributed
to proposal development, data collection, and write up of this study. However,
the corresponding author has prepared the manuscript for publication and
carried out activities during publication process.
Acknowledgements: We would like to thank Debre
Tabor University for supporting this work through financial grant. We would
also thank farmers around Mt. Guna for their valuable
help during data collection.
Abstract: Abyssinian Grass Rats Arvicanthis abyssinicus
and Common Mole Rats Tachyoryctes splendens are preyed upon by the Ethiopian Wolf Canis simiensis.
The aim of this study was to assess distribution, diet and trophic level of Arvicanthis abyssinicus
and Tachyoryctes splendens
on Mount Guna, where wolves have recently become
extinct. Rodents were captured with Sherman trap and identified, and samples
were taken to Debre Tabor University for dissection and diet analysis via
microscopy examination of stomach contents. 110 A. abyssinicus
and 52 T. splendens were captured from the
study area, and the estimated population sizes of A. abyssinicus
and T. splendens in Mt. Guna
computed by Peterson-Lincoln Index were 1,364 and 416, respectively. In
addition, 379 burrows (203 of A. abyssinicus
and 176 of T. splendens) were counted.
Both species were observed to consume plants and arthropods, with plants
predominant. We recommend that intensive studies should be carried out to
determine the effects of rodent communities upon Mt. Guna
afroalpine and subafroalpine
ecosystems.
Keywords: Afroalpine, diets, Mt. Guna, stomach analysis, subafroalpine.
Afan Oromo abstract: Guduunfaa: Gosoota
hantuutaa keessaa tuqaa (Tachyoryctes splendens) fi hantuutni huuraa (Arvicanthis abyssinicus) soorata jeedala diimtuu (Canis simiensis) keessaa isaan tokko.
Kaayyoon qo’annoo kanaa bakka duraan
jeedalli diimtuu irra jiraachaa turte keessatti iddoowwan hantuutotni armaan olii kun
qubatan, nyaata isaanii fi sadarkaa saaphaphuu nyaataa isaan irratti argaman adda baasuu ture.
Hantuutotni kunneen erga kiyyeeffamanii booda nyaata garaacha
isaanii keessatti argamu adda baasuuf
gara Yuunivarsiitii Dabra Taaboritti geeffaman. Bu’aan qo’annichaa akka mul’isutti hantuuta huuraa lakkoofsaan 110 ta’anii fi tuqaa lakkoofsaan 52 ta’antu bakka qo’annoon kun itti gaggeeffame
sanaa qabame. Lakkoofsi hantuutota sanaa yaroo ‘Peterson-Lincoln Index’n shallagamu kan hantuuta huuraa
1,364 fi kan tuqaa 416’tti tilmaamama. Dabalataanis, boolla hantuutaa gara 379 (kan hantuuta
huuraa 203 fi kan tuqaa 176) ta’antu bakkichaa adda ba’e. Caalatti biqiltoota kan sooratan ta’anis, gosootni hantuutotaa kun mukootaa fi ilbiisotaa garaagaraa akka nyaatantu qo’annoo kanaan mirkanaa’e. Bu’aa qo’annoo kanaarratti hundaa’uun dhiibbaan gosootni hantuutaa kun Gaara Gunaa
irraan ga’aa jiran gadi fageenyaan
akka qoratamu yaada dhiyeessina.
INTRODUCTION
Rodents exploit a wide range of
habitats throughout the world (Lange et al. 2004). Their distribution and
abundance is influenced by vegetation structure and composition (Gebresilassie et al. 2004; Kannan & James 2009),
which influence micro-climate and provide food and cover against predators
(Hansson 1999).
Ethiopia is a physically and biologically diverse
country in Africa, where differences in climate and topography have resulted in
a wide diversity of habitats and species (Tedla 1995;
Abunie 2000). Of 284 mammals identified from
Ethiopia, rodents comprise 25% and contribute about 84% of the total endemic
species (Yalden & Largen 1992; Bekele et al.
1993; Bekele & Leris 1997; Laverenchenko
et al. 1997). Ecological knowledge about these rodent, including their
distribution and abundance, is limited (Habtamu &
Bekele 2008).
Distribution and abundance of rodents can be estimated
by trapping and recording of animals signs, holes, or related elements that
infer the presence of animals (Krebs 1978; Rabinovich
1980). The best techniques are those based on the use of capture traps and
recording of signs, due to the crepuscular habits of rodents (Aplin et al. 2003).
Rodents are omnivorous, mainly consuming plant parts
such as fruits and seeds, as well as small arthropods (Best et al. 1993).
Techniques commonly used to assess the diets of rodents include field
observations of partially consumed organisms (Meyer & Shiels
2009), captive-feeding trials (Shiels 2011), and
stomach content analysis (Ruffino et al. 2011). While effective, stomach
content analysis has in a relatively small number of studies (Hope &
Parmenter 2007).
The Ethiopian Wolf Canis
simensis is a Critically Endangered medium-sized
canid highly adapted to live in Ethiopian afroalpine
and subafroalpine ecosystems above altitudes of 3,000
m, and it is the almost exclusive predator of high altitude rodents (Marino et
al. 2010; Yihune & Bekele 2012). The Ethiopian
Wolf Conservation Program (EWCP) team confirmed the extinction of this species
from Mt. Guna in 2011, after several years of serious
decline (IUCN/SSC 2011). A preliminary survey by Debre Tabor University staff
in 2014 confirmed that the Ethiopian Wolf had not been seen for the last four
years in Mt. Guna (Sillero-Zubiri
& Macdonald 1997). As a result, rodent numbers were observed to have
increased on Mt. Guna, possibly resulting in
ecosystem disturbance.
Fluctuations in rodent population density can have
major impacts on the dynamics of their food (arthropods and plants) and
predators (Ims & Fuglei
2005). If the population density of rodents in an ecosystem exceeds the
carrying capacity, prey can be affected by overconsumption and the ecosystem
can collapse unless control measures are taken. Conversely, if the population
density of rodents is too low to sustain predators, they can become locally extinct.
The aim of the present study was to assess distribution, diet and trophic level
of two rodent species on Mt. Guna known to be prey of
the now-extinct Ethiopian Wolf population.
MATERIALS & METHODS
Study area
Mt. Guna is located in South
Gondar Zone at 11.7500N, 38.2500E, with a peak rises to
4,231 m (Figure 1). Mt. Guna has afroalpine
(3,500–4,231 m) and subafroalpine (3,200–3,500 m)
ecosystems suitable to Ethiopian Wolf Canis
simensis and mountain rodents. The area coverage
is 210 km2 of land above 3,200 m, and 110 km2 above 3,400
m, but no more than 40 km2 above 3,800 m which is good habitat for
Ethiopian Wolf (Sillero-Zubiri & Macdonald 1997; Belste et al. 2012)
Mt. Guna is surrounded by
six districts of South Gondar Zone namely Lay and Tach Gayint,
Farta, East Este, Simada,
and Dera. The economy of the people living in those
districts is mainly dependent on subsistence Agriculture. They cultivate crops
like barley, wheat, bean, potato, and own livestock including cattle, sheep,
donkey, and horse. The vegetation of Mt. Guna
includes different grass species like ‘guassa’ and
tree species with many animal lives including rodents, jackals, gelada baboons,
hyenas, and rock hyraxes. The area is also inhabited by giant lobelia tree
which is known to be the unique characteristic to afroalpine
and subafroalpine ecosystems (ALZR 2006; Belste et al. 2012).
Data collection
Before starting the field work, permission for rodent
collection and habitat observation was acquired from South Gondar Zone Wildlife
Conservation Authority Office, Ethiopia. A quantitative cross-sectional
study was conducted in the dry season of 2015 on Mt. Guna,
northwestern Ethiopia. Samples were collected at
three localities: bottom, middle and top of Mt. Guna.
Three 60 X 60 m trapping grids (1.08 ha) were set at each site, and 36 Sherman
traps were placed: 12 at top of afroalpine, 12 at
middle, and 12 at bottom of subafroalpine ecosystem
in the sampling period. Traps were baited with a mixture of rolled oats and peanut
butter. The traps were set in the late afternoon (1500–1600 h) and left in the
sampling sites for three consecutive days and nights. They were checked during
the morning (0600–1200 h) and afternoon (1600–1800 h). Capture terms consisted
of two sampling periods (February and March) separated by a month interval
without trapping. All captured rodents were used for species identification,
distribution, as well as stomach contents analysis according to the standard
(Hope & Parmenter 2007). After identification done through morphological
characteristics including differences in body size, shape, fur texture and
colour (Aplin et al. 2003; Jonathan 2004), only two
species of rodent namely Abyssinian Grass Rat A. abyssinicus,
and Common Mole Rat T. splendens were counted,
marked and released to their respective habitats with other trapped rodents
when encountered. In addition, active burrows (fresh burrows that have marks of
rodents and freshly excavated soil and cut parts of various plants) of the
above rodents were identified and counted from the same grids for further
determination of distribution and abundances. Percentage of active burrows in
the area was estimated as:
Population of active burrows %= (Number of active
burrows/Total burrows examined all over) * 100 (Feliciano et al. 2002; Desoky 2007).
Eight rodents (four for each species) were taken to
Debre Tabor University, laboratory of Department of Biology, for dissection to
remove the gastro-intestinal contents. Diet analysis was carried out using the method
of DeBlasé & Martin (1981). Accordingly, contents
of the stomach were placed in a petri dish and thoroughly mixed to loosen
material to give all constituents a uniform distribution. Then the contents
were examined under a light microscope at 20x magnification to identify food
items. Four fields of observation were examined. The diagram of food web was
also drawn and trophic level of rodents was shown for Mt. Guna
based on current result and the literature.
Since Belste et al. (2012)
reported the presence of Ethiopian Wolf in Mt. Guna
after the report of species extinction (IUCN/SSC 2011), interview questions
were administered to check the presence-absence of the species. Fifty local
people were purposively selected and interviewed to know when the wolf was
observed for the last time in the study area and the reason for extinction. The
local people were purposively selected based on the knowledge of the wolf,
distance from the study area (nearby) and residence in the adjacent villages.
Data analysis
Distribution of A. abyssinicus
and T. splendens was calculated with
descriptive statistics. Number of rodents and their burrows collected from the
three sites was shown on table and graph. Absolute number of the rodents in a
population was calculated by Peterson-Lincoln index (Seber
1982) as follows. , where N= population size estimate, M=
marked individuals released, S= size of second sample captured, and R= marked
animals recaptured.
Food web for the overall study area was shown by table
and diagram. Independent two-sample t-test on Minitab software was used to
compare food items eaten by both species. In addition, Independent two-sample
t-test on R-software was used to compare distribution of both species among the
three sites. Statistical value of 0.05 was taken as significance level.
RESULTS
Rodent species identification and distribution
In the present study, two species of rodent namely
Abyssinian Grass Rat and Common Mole Rat were collected from afroalpine and subafroalpine
ecosystems of Mt. Guna (Image 1). From all sites, a
total of 162 rodents were captured during the first session of study period.
From these, 110 (52.73% from the top, and 47.27% from the middle) were A. abyssinicus and 52 (23.08% from the top, 26.92% from
the middle, and 50% from the bottom) were T. splendens.
Regarding to the distribution, high number of A. abyssinicus
(52.73%) was collected from the peak of the mountain following the
middle (47.27%); however, low number of T. splendens
(23.08%) was collected from the top, even though there was no significant
differences among the three sites (p= 0.41, df=
2.22). On the other hand, high number of T. splendens
(50%) was sampled from the bottom of Mt. Guna from
where no single A. abyssinicus was collected
as indicated on Table 1. In addition, 124 A. abyssinicus
and 48 T. splendens were captured in the
second session of the study period with almost similar distribution as of first
session (Table 2). The overall estimated population number of A. abyssinicus and T. splendens
in the study area computed by Peterson-Lincoln Index was 1,364 and 416,
respectively.
A total of 379 burrows, of which 179 were active, were
counted from the same grids laid in total of 3.24 ha to sample rodents. As
shown on Table 1, there was no A. abyssinicus burrow
counted from the bottom of the study area whereas 104 (59.09 %) T. splendens burrows were counted from the same site.
However, there was high population of A. abyssinicus
at the top (n= 107, 52.63 %) followed by the middle (n= 96, 47.37 %) of the
mountain. These distribution differences of burrows among the three sites were
also not significant (p= 0.84, df= 2). Out of the
total burrows of each rodent, 51.14 % of them were active for T. splendens, whereas 43.84 % were active for A. abyssinicus. Such high percentage of active burrows
supports the existence of significant numbers of both rodents in the study
area.
Stomach content analysis
Eight rodents: four T. splendens
and four A. abyssinicus were dissected and stomach
contents were taken. Diets of each rodent were identified into plant and
arthropod types under the light microscope. Accordingly, T. splendens and A. abyssinicus
have been identified to consume both plants and arthropods (Table 3). In
contrast, there was no significant difference on the consumption of arthropods
between both species (p= 0.466, df= 4). In addition
to the stomach content analysis, the remains of leftover of plant parts and
arthropod parts after their feeding were observed on the way to their burrows
during field work.
Habitat observation
During data collection, the authors have repeatedly
observed Mt. Guna afroalpine
and subafroalpine ecosystems. Destruction of grasses
and other vegetation due to high population of rodents, rock hyraxes and
livestock at the bottom and middle of the ecosystems was observed (Figure 2).
Furthermore, the same condition was seen at the top of afroalpine
due to high populations of rodents and some groups of Gelada Theropithecus gelada, endemic to Mt. Guna, foraging in the same habitat. Moreover, rodents
living adjacent to agricultural lands were observed to migrate to agricultural
fields and damage farmers’ crops.
Assessment on the extinction of Ethiopian wolf
Side by side with data collection of rodents in Mt. Guna, 50 respondents were interviewed to check whether
Ethiopian Wolf is present or locally extinct. All interviewees assured the
local extinction of the wolf by habitat destruction in spite of other factors
such as human killing, rabies virus and climate change they were asked. Most of
the respondents had observed the wolf between 6–8 years followed by before 10
years. All of them responded that they have never seen the wolf since four
years (Figure 2). They said that a single wolf has been observed for years
until total disappearance from the study area in 2011.
DISCUSSIONS
In the present study, distribution, diets and trophic
level of two species of rodents, the Abyssinian Grass Rat and Common Mole Rat,
were assessed. Both species were identified in afroalpine
and subafroalpine ecosystems of Mt. Guna. Mark-recapture method indicated that there was high
population of T. splendens at the bottom,
while A. abyssinicus was abundant at the peak
of Mt. Guna. In agreement to the current study, Belste et al. (2012) identified Abyssinian Grass Rat and
Common Mole Rat along with common home rat Arvicanthis
spp., Harrington’s Rat Desmomys harringtoni, Harsh-furred Rat Lophuromys
flavopunctatus, and White-footed Rat Stenocephalemys albipes
from the study area.
Since active burrows give an idea of the number of
rodents living in the study area (Desoky 2007),
burrow count was also carried out to support the mark-recapture method. The
result of burrow counts confirmed the existence of high population of A. abyssinicus and T. splendens
in the study area. Like trap method, burrow count method also indicated that
there was high population of T. splendens at
the bottom, but A. abyssinicus was totally
absent from the bottom grids though field observation depicted the existence of
it in smaller number. However, there was high distribution of A. abyssinicus at the top and middle of the ecosystems.
Study conducted by Yihune & Bekele (2012) in afroalpine habitat of Simien Mountains National Park (SMNP)
also identified significant number of A. abyssinicus
and T. splendens.
Environmental degradation due to high population of
rodents as a result of the extinction of wolf predator from Mt. Guna was clearly seen through field observation. In support
to this, study shows that cyclic fluctuations in population density of rodents
have major impacts on the dynamics of their food and vertebrate predators (Ims & Fuglei 2005). In
addition, high population of livestock was observed in the ecosystems. Such
pressures can lead to massive destruction, depletion and degradation of
wildlife habitats as well as severe reduction in wildlife population (Hillman
1993). Furthermore, field observation and interviews of local farmers showed
that those rodents living in the study area migrated to nearby agricultural
fields for searching of additional foods. Such migration observed to cause crop
damage in agricultural fields even though it was not quantified by the present
study.
Out of the total diets consumed by both species, there
was high frequency of plant parts (not identified into species level) in their
stomach contents which assures the fact that the majority of their diet is
plant. However, more plant parts were consumed by Common Mole Rats than by
Abyssinian Grass Rats. Even though both species consume arthropods (not
identified into species level), it was significantly less when compared to
plant parts. In agreement to the current study, Best et al. (1993) identified
that rodents are omnivorous animals mainly consuming large quantities of plant
parts. This might be due to the availability, selectivity, and palatability of
plant diets in afroalpine and subafroalpine
habitat as already stated by Beyene (1986) for other
species of the Tachyoryctes genera.
Based on the current result of stomach content
analysis and other published literatures, trophic levels and food web have been
diagrammatically shown for the study area. Besides to the stomach content
analysis, diets of animals existing in Mt. Guna were
reviewed and summarized in Table 4. Based on the summary, a diagram of food web
was drawn (Figure 3).
As shown on Figure 4, T. splendens
and A. abyssinicus consume both plants and
arthropods, hence grouped under omnivorous animals (2nd, 3rd
and even more trophic levels). However, it is difficult to determine specific
position of omnivores’ trophic level since they consume materials from
different trophic levels of the food web (Williams & Martinez 2004).
Ethiopian Wolf Canis
simensis, which is endemic to Ethiopia, is the
rarest canid in the world with a total global population of 500 individuals and
classified as ‘Endangered’ on the IUCN Red List of Threatened Species (Marino
& Sillero-Zubiri 2013; Marino et al. 2017). The
wolf highly adapted to live in afroalpine and subafroalpine ecosystems above altitudes of 3,000 m, and is
almost exclusively the predator of high altitude rodents (Marino et al. 2010; Yihune & Bekele 2012). Study shows that Ethiopian Wolf
is an important flagship species for conservation of the afroalpine
biodiversity (IUCN/SSC 2011), but faces serious threats to its survival in its
ecosystem. In the present study, all the interviewees agreed the local
extinction of Ethiopian Wolf Canis simensis due to habitat degradation. According to the
respondents the single wolf was seen in 2011 for the last time. This agrees
with the report by IUCN/SSC (2011) on its extinction from Mt. Guna although Belste et al.
(2012) claimed to identify the wolf from the same study area referring to the
local community. For long, the ecosystems of Ethiopian highlands had been
threatened by overpopulation, overgrazing, and crop cultivation (Leipzig 1996).
Similarly, Mt. Guna is currently under human induced
threats from agricultural expansion, livestock overstocking, overharvesting of
natural resources and settlements (Belste et al.
2012) that might mainly resulted in the local extinction of Ethiopian
Wolf.
CONCLUSION
In the current study, the distribution, diets and
trophic level of two rodent species namely Abyssinian Grass Rat and Common Mole
Rat was assessed from Mt. Guna afroalpine
and subafroalpine ecosystems. The results from
Sherman traps and burrows count showed that both species were identified to be
highly populated in the study area. Stomach content analysis revealed that both
species consume both plants and arthropods, hence grouped under omnivorous
animals (2nd, 3rd and even more trophic levels).
Furthermore, Ethiopian Wolf was also confirmed to be locally extinct from Mt. Guna due to habitat degradation.
Based on the current study, we recommend that
intensive studies should be carried out to analyse the effect of rodent
community on Mt. Guna ecosystems due to the
extinction of Ethiopian Wolf. To reduce effects of rodent pests and
environmental degradation in the present study area, the long run rodent prey
control by their predator, and habitats conservation should also be taken into
consideration. Further study that include different seasons and impact of pest
rodents on agricultural lands should also be carried out in Mt. Guna.
Table 1. Number of rodents collected in first session
and total burrows counted from the three sites of Mt. Guna.
|
No. of
rodent
No. of burrows |
||||
|
Grids |
A. abyssinicus
|
T. splendens |
A. abyssinicus |
T. splendens |
|
Top |
58 (52.73%)
|
12 (23.08%) |
107 (52.63%) |
12 (6.82%) |
|
Middle |
52 (47.27%) |
14 (26.92%) |
96 (47.37%) |
60 (34.09%) |
|
Bottom |
--- |
26 (50%) |
--- |
104 (59.09%) |
|
Total |
110 (100%) |
52 (100%) |
203 (100%) |
176 (100%) |
|
|
df= 2.22
p= 0.41 |
df= 2 p= 0.84 |
||
Table 2. Number of first captures and recaptures of A.
abyssinicus and T. splendens
by Sherman traps from three sites (three grids from each site= S1, S2 and S3)
of Mt. Guna
|
Species
|
Site |
First capture (marked individuals and released) |
Second capture |
Marked animals recaptured |
|
A. abyssinicus |
Top |
|
|
|
|
|
S1 |
23 |
27 |
2 |
|
|
S2 |
20 |
19 |
1 |
|
|
S3 |
15 |
21 |
1 |
|
|
Total |
58 |
67 |
4 |
|
|
Middle |
|
|
|
|
|
S1 |
15 |
20 |
2 |
|
|
S2 |
20 |
19 |
2 |
|
|
S3 |
17 |
18 |
2 |
|
|
Total |
52 |
57 |
6 |
|
|
Overall total |
110 |
124 |
10 |
|
T. splendens |
Top |
|
|
|
|
|
S1 |
4 |
5 |
-- |
|
|
S2 |
5 |
2 |
-- |
|
|
S3 |
3 |
4 |
1 |
|
|
Total |
12 |
11 |
1 |
|
|
Middle |
|
|
|
|
|
S1 |
6 |
8 |
1 |
|
|
S2 |
3 |
5 |
1 |
|
|
S3 |
5 |
4 |
-- |
|
|
Total |
14 |
17 |
2 |
|
|
Bottom |
|
|
|
|
|
S1 |
7 |
5 |
-- |
|
|
S2 |
9 |
7 |
1 |
|
|
S3 |
10 |
8 |
-- |
|
|
Total |
26 |
20 |
1 |
|
|
Overall total |
52 |
48 |
4 |
Table 3. Frequency of plants and arthropods diet
identified from the stomach of four T. splendens and
four A. abyssinicus collected from Mt. Guna.
|
Rodent species |
|
Frequency of plant parts |
Frequency of arthropod parts |
|
T. splendens (T) |
T1 |
38 (73.08%) |
14 (26.92%) |
|
|
T2 |
53 (79.10%) |
14 (20.90%) |
|
|
T3 |
41 (82%) |
9 (18%) |
|
|
T4 |
48 (90.56%) |
5 (9.44%) |
|
Average |
45 (81.08%)** |
10.5 (18.92%)* |
|
|
A. abyssinicus (A) |
A1 |
31 (75.61%) |
10 (24.39%) |
|
|
A2 |
28 (71.79%) |
11 (28.21%) |
|
|
A3 |
25 (64.10%) |
14 (35.90%) |
|
|
A4 |
34 (69.38%) |
15 (30.62%) |
|
Average |
29.50 (70.24%)** |
12.5 (29.76%)* |
|
** Significant at 0.05 significance level (P= 0.017, df= 3)
* Not significant at 0.05 significance level (P=
0.466, df= 3)
Table 4. Major animals identified from Mt. Guna and their food items.
|
Animal species (Belste et
al. 2012) |
Food items |
Identification of food items |
|
Rodents |
|
|
|
Common Mole Rat Tachyoryctes
splendens |
Plant parts, arthropods |
Current Lab work |
|
Abyssinian Grass Rat Arvicanthis
abyssinicus |
Plant parts, arthropods |
Current Lab work |
|
Harrington's Rat Desmomys
harringtoni |
--- |
xx |
|
Harsh-furred Rat Lophuromys
flavopunctatus |
Arthropods, small vertebrates, plant matter |
Dieterlen 1976 |
|
White-footed Rat Stenocephalemys
albipes |
--- |
xx |
|
Carnivores |
|
|
|
Common Jackal Canis
aureus |
Rodents,
ungulates, livestock |
Bošković et al. 2013 |
|
Black-backed Jackal Canis
mesomelas |
Rodents, ungulates, birds, Reptiles, insects, grass |
Humphries et al. 2015 |
|
Ethiopian Wolf Canis
simensis* |
Rodents, sheep (rare) |
Ashanafi et al. 2005 |
|
Caracal Caracal caracal |
Rodents, birds, ungulates |
Braczkowski et al. 2012 |
|
Wildcat Felis silvestris lybica |
Shrews, rabbits, birds, reptiles, rodents, insects |
Moleón & Gil-Sánchez 2003 |
|
Serval Leptailurus
serval |
Rodents, antelopes, insects, reptiles |
Ramesh & Downs 2014 |
|
Leopard Panther pardus |
Livestock, monkey, rodents, birds, hares |
Kshettry et al. 2018 |
|
Spotted Hyena Crocuta
crocuta |
Livestock, human, porcupine, hare, bushbuck, kudu,
waterbuck, common duiker |
Yirga et al. 2015 |
|
Striped Hyena Hyaena hyaena |
mammals, rodents, insects, livestock |
Alam & Khan 2015 |
|
Common Dwarf Mongoose Helogale
parvula |
Insects,
spiders, scorpion, lizards, snakes, small birds and rodents |
Ramulondi & Zengeya 2014 |
|
African civet Civettictis
civetta |
mammals, birds, reptiles, insects, plant parts |
Tadesse et al. 2017 |
|
Primates |
|
|
|
Gelada baboon Theropithecus
gelada |
Grasses, herbs, other plant parts |
Kelil et al. 2018 |
|
Vervet Monkey Cercopithecus aethiops |
Invertebrates, plant parts |
Tournier et al. 2014 |
|
Olive baboon Papio
anubis |
Plant parts, insects, birds, mushrooms |
Okecha & Newton-Fisher 2006 |
|
Herbivores |
|
|
|
Common Duiker Sylvicapra
grimmia |
Herbivores feed on vegetation such as grasses,
fruits, leaves, roots, bulbs, etc. |
Karmiris et al. 2011 |
|
Klipspringer Oreotragus
oreotragus |
||
|
Rock Hyrax Heterohyrax
brucei |
||
|
Birds |
|
|
|
Hooded Vulture Necrosyrtes
monachus |
A review by Lopes et al. (2016) identified all diet
types and food categories for tropical birds. The study revealed 23 food
types frequently eaten by birds and proposed standard names for birds (e.g., granivore, frugivore, and insectivore). Accordingly, plant
diet consumed by birds mainly are fruits, seeds, grains, plant fluids,
leaves, buds, grasses, nectar, pollen, etc. In addition, birds also consume
insects including ants, cockroaches, termites, locusts, bugs, beetles, flies,
butterflies, dragonflies, bees, wasps, stoneflies, and mayflies. Birds of
prey eat animal flesh including fish, reptiles,mammals,
birds, insects, and molluscs. |
|
|
Greater Spotted Eagle Aquila clanga |
||
|
Red-throated Bee-eater Merops
bullocki |
||
|
Blue-winged Goose Cyanochen
cyanopterus |
||
|
Wattled Ibis Bostrychia
carunculata |
||
|
Black-winged Lovebird Agapornis
taranta |
||
|
White-collared Pigeon Columba albitorques |
||
|
Ring-necked Dove Streptopelia
capicola |
||
|
Red-eyed Dove Streptopelia
semitoquata |
||
|
Thick-billed Raven Corvus
crassirostris |
||
|
Fan-tailed Raven Corvus
rhipidurus |
||
|
Abyssinian Long Claw Macronyx
flavicollis |
||
|
Abyssinian Catbird Parophasma
galinieri |
||
|
Ankober Serin Serinus
ankoberensis |
||
|
White-cheeked Turaco Tauraco
leucotis |
||
|
Moorland Francolin Francolinus
psilolaemus |
||
|
Red-fronted Parrot Poicephalus
gulielmi |
||
|
African Firefinch Lagonosticta
rubricate |
||
|
Ethiopian Swallow Hirundo
aethiopica |
||
|
Widowbird Euplectes
orix |
||
*—Locally extinct | **—No published work on the diets
of the animals.
For
figures & images - - click here
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