Journal of Threatened Taxa | www.threatenedtaxa.org | 26 May 2019 | 11(7): 13850–13867

 

First assessment of bird diversity in the UNESCO Sheka Forest Biosphere Reserve, southwestern Ethiopia: species richness, distribution and potential for avian conservation

 

Mattias Van Opstal 1, Bernard Oosterlynck 2, Million Belay 3, Jesse Erens 4  & Matthias De Beenhouwer 5

 

1,2,4,5Biodiversity Inventory for Conservation (BINCO) vzw, Walmersumstraat 44, 3380 Glabbeek, Belgium.

3MELCA-Ethiopa, P.O. Box: 1519 Code 1250 Addis Ababa, Ethiopia.

55Plant Conservation and Population Biology, Department of Biology, KU Leuven, Kasteelpark Arenberg 31, B-3001 Heverlee, Belgium.

1vanopstalmattias@gmail.com (corresponding author), 2oosterlynckbernard@gmail.com, 3millionbelay@gmail.com, 4esse.erens@outlook.com,
5m.debeenhouwer@gmail.com

 

Abstract: The Sheka Zone in southwestern Ethiopia is covered by some of the largest remaining forests in the Eastern Afromontane biodiversity hotspot.  Owing to the rich biodiversity and a high degree of endemism, it was declared as a biosphere reserve by UNESCO in 2012 and is considered a Key Biodiversity Area.  Detailed knowledge on species diversity and distribution in the reserve is, however, severely limited.  From February to April 2016, an assessment of the bird diversity and distribution in the reserve was made for the first time through point count transects, camera-trap recordings and opportunistic observations.  In total, 244 bird species were identified, of which 19% was only found within the reserve’s designated protected zones.  Our study indicates a remarkable bird species richness across the different habitats in Sheka Forest Biosphere Reserve and can be used as a baseline for future monitoring studies and conservation planning.

 

Keywords: Avifauna, Eastern Afromontane Biodiversity Hotspot, habitat occupation, Horn of Africa, inventory, IUCN.

 

doi: https://doi.org/10.11609/jott.4726.11.7.13850-13867  |  ZooBank: urn:lsid:zoobank.org:pub:A3A5AE48-AC9B-4173-B63F-87D2921E2791

 

Editor: Reuven Yosef, Ben Gurion University of the Negev, Eilat, Israel.             Date of publication: 26 May 2019 (online & print)

 

Manuscript details: #4726 | Received 25 November 2018 | Finally accepted 04 May 2019

 

Citation: Van Opstal, M., B. Oosterlynck, M. Belay, J. Erens & M. De Beenhouwer (2019). First assessment of bird diversity in the UNESCO Sheka Forest Biosphere Reserve, southwestern Ethiopia: species richness, distribution and potential for avian conservation. Journal of Threatened Taxa 11(7): 13850–13867. https://doi.org/10.11609/jott.4726.11.7.13850-13867

 

Copyright: © Van Opstal et al. 2019. Creative Commons Attribution 4.0 International License.  JoTT allows unrestricted use, reproduction, and distribution of this article in any medium by adequate credit to the author(s) and the source of publication.

 

Funding: CEPF (Critical Ecosystem Partnership Fund).

 

Competing interests: The authors declare no competing interests.

 

Author Details: Mattias Van Opstal is an ornitologist and holds a master in Bio-Science engineering. He is an active member of BINCO. He currently works as research associate at ILVO (Institute for agriculture and fisheries) where he leads different marine research projects.  Bernard Oosterlynck is Biologist, active as biodiversity survey coordinator for BINCO during fieldwork in Ethiopia. Specialised in agricultural impact on biodiversity of avifauna and big mammals in Africa.   Jesse Erens is a herpetologist and currently a PhD fellow at Ghent University working on amphibian conservation.  Million Belay is the founder of MELCA-Ethiopia and the Alliance for Food Sovereignty in Africa (AFSA). He is an expert and advocate for forestry conservation, resilience, indigenous livelihoods and food and seed sovereignty.  Dr. Matthias De Beenhouwer is a forest ecologist, working as a project manager on reforestation projects for the ngo WeForest. He holds a PhD on Afromontane coffee forestry from the Catholic University of Leuven, Belgium. He is specialized in forestry systems and has 7 years of experience working in Ethiopia and Southern Africa. He also has experience with standardized biodiversity assessment, mostly of plant and vertebrate taxa.

 

Author Contribution: MDB and MB designed the study, MVO, BO, JE and MDB collected the data, BO and MDB analysed the data. MVO, JE and MDB wrote the manuscript.

 

Acknowledgements: We greatly acknowledge the CEPF (Critical Ecosystem Partnership Fund, Grant No. S14-272) and the KNBV (Royal Botanical Society of The Netherlands) for financially supporting this project.  BirdLife International, IUCN and EWNHS are acknowledged for logistic support, and we are grateful to the EWCA for research permission.  We thank A. Shaweno and all staff of MELCA-Ethiopia for their continued support, hospitality and invaluable help during the fieldwork, as well as all trainees who helped us collecting data: W. Adinew, M. Chegito, B. Ayasho, B. Kidane and G. Kassahun.  Furthermore, we would like to express our gratitude to all clan leaders and local guides for welcoming us on their lands and providing guidance in the field.  We also thank Y. Dellelegn and S. Jones for their valuable comments on bird identifications.

 

Introduction

Ethiopia is recognized among the 35 most biodiverse regions in the world and its biodiversity is renowned for its high percentage of endemism.  The highlands in the southwest, where most of the larger forest tracts remain, are part of the Eastern Afromontane Biodiversity Hotspot (Mittermeier et al. 2011).  Natural habitats are highly diverse in this region, where the forest structure changes along a large elevation gradient (Friis 1992), with moist evergreen Afromontane rainforests presenting the dominant vegetation type, but also including bamboo forests and transitional rainforests leading down to semi-deciduous forests at lower altitudes.  In most areas, the forests are interspersed with wetlands or, at higher altitude, moorlands. Ethiopian natural forests are however rapidly disappearing (Dessie & Kleman 2007; Reusing 2000), with approximately 11.4% or 12,499,000ha of total forest cover left (FAO 2015).

The Sheka Zone in southwestern Ethiopia still harbors some of the largest remaining Afromontane forests in the country (>100,000ha).  Nevertheless, the combination of a rising population, ongoing land-allocation to agricultural investors and a lack of land-use planning are increasing pressure on the remaining natural habitats.  As such, the deforestation rate within Sheka is one of the highest in Ethiopia, with severe impacts on local economy, culture and environment (Woldemariam & Fetene 2007).  Sheka forest is considered a Key Biodiversity Area (Birdlife International 2017) and, in 2012, it was recognized by UNESCO as the Sheka Forest Biosphere Reserve.  This recognition has led to the zonation of the area into core-, buffer- and transition zones (Fig. 1).  These are, respectively, devoted to long-term protection of intact forests (core zones), participatory forest management and low-intensity production (buffer zones), and sustainable human settlement and agriculture (transition zones) (Gole & Getaneh 2011).  The forest furthermore provides an important refuge for the native genetic diversity of wild crop relatives with significant agricultural value.  The most prominent example is the indigenous wild coffee Coffea arabica, which can still be found in reasonable densities in the broadleaf forest of Sheka, but also other wild crop relatives that are imperative for local food provisioning such as Enset or ‘False Banana’ Ensete ventricosum and Ethiopian Cardamom Aframomum corrorima.  All combined, there are strong incentives to safeguard this forest also from an economic and agricultural perspective (De Beenhouwer et al. 2013; Aerts et al. 2015).

Biodiversity and conservation research has seen a recent increase in southwestern Ethiopia, mainly in relation to agroforestry (e.g., Hundera et al. 2013; Tadesse et al. 2014); however, biodiversity studies in remote forest regions such as Sheka have been very limited thus far, despite the recognition as a UNESCO biosphere reserve and strong ongoing habitat degradation.  Detailed insights in the diversity, distribution and abundance of species in the area are hardly available.  Likewise, information on the bird diversity in Sheka forest is very scarce, but limited research done in the broader region (e.g., Woldegeorgis & Wube 2012) provides clear indications for a large bird species diversity in remaining forest tracts of southwestern Ethiopia.  Here, we present a first comprehensive inventory of the bird diversity in Sheka Forest Biosphere Reserve, discuss our observations in relation to the delineated management zones, and highlight the biosphere reserve as an understudied yet highly valuable area for bird conservation and continued biodiversity studies.

 

Materials and Methods

From Masha (around 7.7490N & 35.4710E; ca. 2,250m), the largest village in the area and capital of the Sheka Zone, we surveyed a variety of core-, buffer- and transition zones across the three districts, or ‘woredas’, situated in the biosphere reserve (Masha, Anderacha and Yeki).  Our field expeditions took place from 2 February 2016 until 30 April 2016, and nine different ‘kebeles’ (the smallest administrative division) were visited across the three woredas(Table 1).  The humid highlands of southwestern Ethiopia are characterized by a short rainy season from March to April and a long rainy season from June to October, with an average temperature of 18.4°C and yearly precipitation of 1,783mm.  Hence, our expeditions were carried out immediately prior to and during the short rainy season.  Permission for the field work was granted by the Ethiopian Wildlife Conservation Authority (EWCA) at the national level, the head office of the Sheka Zone and by kebele leaders on the local administrative level.  The study was part of a larger expedition to assess the biodiversity in the reserve.

Birds were identified using visual, vocal and camera trap observations. Photo and audio recordings were made to support identification.  When recordings of certain species were lacking, only those with double observations were listed.  Visual and vocal assessments were done during early morning point transect surveys and on an ad hoc basis in all locations visited throughout the expedition.  Because the delineation between core and buffer zones was not always clear in the field, observations herein were collectively assigned to the ‘protected zones’ within the reserve.  Assessments were carried out covering a wide variety of habitats.  These were divided into seven categories for a provisional overview of species’ habitat occupation throughout the reserve (Table 2).  Early morning point transect surveys consisted of six counts of 10 minutes, interspersed by five minutes of walking in a predetermined direction.  All birds seen and/or heard within a perimeter of 25 meters around the observer were noted.  In this way, a total of 74 point transect surveys were carried out, with one survey always restricted to the same habitat.  Species identification was done using the Helm field guide ‘Birds of the Horn of Africa’ (Redman et al. 2011) as a main reference.  Occasional unknown sounds were recorded and identified afterwards using the xeno-canto database (http://www.xeno-canto.org).

Camera trap monitoring was done with 16 camera traps in 28 different locations (see Fig. 1) for a total of approximately 510 camera trap days.  Camera trap locations were selected based on their potential to monitor mammal diversity, but additional bird observations were made of crepuscular species and analysed as part of the present study.

 

Results

We recorded a total of 244 bird species from 55 different families in the Sheka Forest Biosphere Reserve (Table 3; Images 1–4).  Of the species recorded in the reserve during our fieldwork, 47 species or 19% were only found in the designated protected zones.  All other species were found across a variety of management zones.  Of the 155 species identified during the point transect surveys, 16 species were observed across all studied habitats, of which Bradypterus cinnamomeus (89.2% of surveys), Turdus (olivaceus) abyssinicus (83.8%),and Zosterops poliogastrus kaffensis (78.4%) were the most common bird species identified during the surveys.  Riverine forest was the most species-rich habitat sampled with on average 24.3 species sampled per survey, while bamboo forest was the least species rich habitat with an average of 13.4 species recorded per survey (Table 2).  Based on our observations, the main habitat types used by each species are noted, except for the species encountered on migration, for which no habitats could be determined (Table 3).

Eleven bird species that were recorded during the surveys are considered threatened based on the IUCN Red List.  With the notable exception of the recorded vultures, these observations largely stem from within the designated protected zones of the reserve.  Details on these species and their identification are discussed below:

Necrosyrtes monachus (Critically Endangered) (Image 1C)

A smaller brown vulture, identified based on its naked pink head and whitish-grey ‘hooded’ hindneck and nape.  It is common and still very abundant around settlements in the region, but rather rare in a variety of other habitats.  Like the other African vultures listed below, it is severely threatened by a combination of factors, including land conversion, active persecution as well as secondary poisoning.

 

Trigonoceps occipitalis (Critically Endangered)

A rather large blackish vulture with contrasting white belly and large red-colored bill.  Singles and pairs are uncommon but found to be widespread in a variety of habitats including settlements.

 

Gyps africanus (Critically Endangered) (Image 1D)

A typical vulture with a bright brown back, dark brown plumage, dark bill and down feathers on the neck.  Seen in groups of up to 20 birds but also often in the presence of other vulture species. Common and widespread in a variety of habitats, most numerous around settlements.

 

Gyps rueppellii (Critically Endangered)

This vulture is similar to Gyps africanus but easily distinguished based on its yellow bill and scaled appearance in adult birds caused by bright edges on dark feathers.  Rather uncommon, but widespread and present in a variety of habitats including settlements.

 

Torgos tracheliotus (Endangered)

A very large, dark brown vulture with a pink head that shows distinctive skin folds.  Pairs and solitary birds were encountered only a limited number of times around smaller settlements and agricultural areas.

 

Aquila nipalensis (Endangered)

A large eagle with brown upper parts and blackish flight feathers, larger and darker than Aquila rapax.  Observed and photographed on only one occasion while on migration northwards on 18 April 2016 above a highland moorland at Gandochi. 

 

Polemaetus bellicosus (Vulnerable)

A very large brown eagle with white body underparts.  Only one sighting in a wetland in the protected zone of Shato where a territorial pair was seen and heard in flight on 24 April 2016.

 

Balearica pavonina (Vulnerable)

An unmistakable crane with predominantly black body plumage and a crown of golden feathers. Limited number of sightings on a single day during a wetland inventory around the town of Masha.

 

Terathopius ecaudatus (Near Threatened)

Easily recognised in flight from below, based on the black body plumage, black and white wings and chestnut tail.  Observed only one time at Shato forest (south) and two times in highland moorland at  Gandochi, where a male was photographed on 30 March 2016.

 

Stephanoaetus coronatus (Near Threatened) (Image 1F)

Large eagle with crest, giving the head a rather triangular appearance. Barred black and white from below, with chestnut underwing coverts.  Widespread and common in the core forested areas, very rare elsewhere.  Both juveniles and adults were seen and photographed on several occasions throughout the study.

 

Rougetius rougetii (Near Threatened) (Image 1H)

A brown rail with white undertail coverts.  Very common in highland wetlands, also common in Moorlands and along the Gebba river.

 

Several species that were found in the reserve during the monitoring occur only in a very restricted range in Ethiopia.  Although these species are not considered threatened on the IUCN red list nor are endemic, their isolated distribution within Ethiopia and/or occurrence at the extremes of their distribution ranges deserves special conservation attention.  Except for Cinnyris chloropygius, these species were exclusively found within the protected zones of the reserve. 

 

Sarothrura elegans

Most common in forest interior, but also more open woodland types.  Never seen, but regularly heard at night or early morning during the short rainy season.  Sometimes, several males could be heard and were recorded giving a long and low hooting “whoooooooo” lasting approximately three seconds and repeated at intervals of approximately five seconds.

 

Sarothrura rufa

Adult males have a chestnut red head and chest with otherwise black plumage with narrow but striking white streaks.  Adult males were observed two times during an inventory in a wetland around Shato when flushed from about 5m from the observers in a wet grassland.

 

Bradypterus alfredi

Sound recorded at two different locations in highland bamboo forest were uncommon and localized.  A rapid series of short notes all at the same pitch “chit-it chit-it chit-it”.

 

Halcyon malimbica (Image 2E)

A striking blue kingfisher, distinguished from Halcyon senegalensis based on its blue breast-band and more extensive amount of black on its wings.  Rare and secretive, but present around the largest rivers in the area.  Often heard in wetland and riverine forest habitat in Shato forest, and one individual was photographed in lowland riverine forest near Tepi.

 

Anomalospiza imberbis

A small finch-like species.  Males were recognised based on their black bill and yellow head and underparts.  Only observed once in the largest wetland at the side of the Gebba River.  A male was seen on 28 February 2018 for approximately 30 seconds sitting on top of a shrub at 15m from the observers during a wetland survey.

 

Cinnyris chloropygius

Males showed a metallic green head, breast and upper parts, a red breast-band and olive belly. Uncommon in open riverine woodland in the lowlands of Tepi, where one territorial male was seen actively foraging during a riverine forest survey by several observers.

Twelve of the bird species observed inside the reserve are considered endemic to the Horn of Africa.  All of these endemic species were encountered regularly within suitable habitat.  Details on species identification are listed below (except for Rougetius rougetii, already discussed above):

 

Bostrychia carunculata

A dark ibis with white shoulder patches and a small wattle hanging from its throat.  Common and abundant around highland wetlands and grasslands.

 

Pternistis castaneicollis

A large francolin with black forehead and creamy white belly.  Uncommon but widespread in a variety of open woodland and forest edges, where often identified by its early morning call.  On one occasion a large group (six birds) was seen in a tea plantation near the Gebba River. 

 

Poicephalus flavifrons (Image 2C)

A medium-sized green parrot, identified by the presence of yellow colouring on the head. Common in a wide variety of forest and woodland, rare around farmland.

 

Agapornis taranta (Image 2D)

A bright green lovebird with green rump and red forehead.  Common in highland woodland, rather rare in a variety of other habitats.

 

Lybius undatus

A barbet with red forecrown and barred plumage.  Rare in open highland forest but common in lowland forest areas near Tepi.

 

Dendropicos abyssinicus

Small woodpecker with green back, heavily barred wings and bright red rump.  Common in a variety of highland forest where identified and photographed on several occasions during the study.

 

Melaenornis chocolatinus

A large, dark grey-brown highland flycatcher with conspicuous yellow eye.  Very common around settlements and a wide variety of other highland habitats.

 

Cisticola (galactotes) lugubris

A cisticola with black and grey streaked mantle and rufous crown.  Extremely common and abundant around wetland, highland moorland and big rivers.

 

Parophasma galinieri

A distinctive grey bird with whitish forehead and orange-red undertail coverts.  Common in highland bamboo forest, where recorded in high densities in forest edges around moorlands, very rare elsewhere.

 

Oriolus monacha (Image 4B)

A large black-headed oriole with grey wing panel.  Very common in a wide variety of highland habitats, not restricted to forests.

 

Corvus crassirostris

A large raven with white patch on nape and very large bill.  Common and abundant around settlements and farmland, rare around wetlands and open forest and not recorded from the core zones.

 

Discussion

This study highlights the importance of the Sheka Forest Biosphere Reserve for globally threatened and Ethiopian endemic bird species, and in particular raptors and vultures.  The results not only emphasize a high species richness in the reserve, but also indicate the importance of the proposed zonation, with increased control and protection, for bird conservation.  Our findings are comparable to other recent ornithological studies in Ethiopia (e.g., Engelen et al. 2017; Rodrigues et al. 2018), showing a structurally diverse landscape, mostly in traditional low-intensity use, supporting a diverse range of bird species, and with undisturbed forest habitats and wetlands presenting a central refuge for vulnerable range-restricted and specialist bird species.

Our inventories were nevertheless confined to the short Ethiopian rainy season, as well as a subset of kebelesand transition-, buffer-, and core zones.  Additional bird species, including seasonally present migrants, can undoubtedly be recorded during future studies in different periods and subregions.  For instance, two endemic red-listed species, expected to occur in the reserve based on distribution maps, were not found (Macronyx flavicollis and Cyanochen cyanoptera).  More extensive surveys, specifically during the long rainy season and in the vast moorlands in the eastern highlands of Anderacha woreda might still indicate their continued presence.  In addition, point transect surveys were mainly conducted to map species diversity and distributions across habitats, but were inadequate to accurately characterize the relative abundance of species in the reserve.  Thus, our study provides a first indication of bird species richness in Sheka forest, and is a baseline that needs complementary monitoring studies to provide more detailed insights in its species composition, population sizes and dynamics.  Our study also showed the added value of camera trapping to record crepuscular species, with Pternistis squamatus and Zoothera piaggiae only being visually observed through camera trap observations.

The large elevation and climatic differences that are present in the reserve add up to a large habitat variation and exceptionally rich bird diversity, underlining the protected status assigned to Sheka forest and the urge to safeguard its habitats from ongoing degradation.  Our observations furthermore emphasize the understudied nature of this remote biosphere reserve and the importance of continued biodiversity studies to inform conservation planning.  The forests of Sheka provide innumerable services to local communities and many people are directly relying on forest resources for their subsistence.  As a result, the forests have been sustained through a long tradition of natural resource management (Woldemariam & Fetene 2007), making Sheka Forest Biosphere Reserve an ideal subject for directed long-term and community-based initiatives to conserve some of the largest remaining Afromontane rainforests.

 

Table 1. An overview of the locations visited in Sheka Forest Biosphere Reserve
during the inventory, highlighting the central areas and field camps around
which search efforts were concentrated and their altitude as approximated by GPS readings.

 

Woreda

Location/kebele

GPS

Altitude (m)

Masha

Masha

7.7490N & 35.4710E

2293

 

Ateso

7.7110N & 35.4500E

2332

 

Shato forest (north)

7.8560N & 35.5060E

1681

 

Shato forest (south)

7.8030N & 35.5510E

1712

 

Karina

7.8590N & 35.3390E

2176

 

Atele

7.7070N & 35.4070E

2385

Anderacha

Gecha

7.5620N & 35.4040E

2231

 

Gandochi

7.4170N & 35.4250E

2576

Yeki

Tepi (and Gilo River)

7.1980N & 35.4250E

1097

 

 

Table 2.The studied habitat categories, including the number of point transect surveys conducted per habitat
and the average number of bird species recorded per survey.  Surveys were not focussed on settlements (Se)
and grazing lands (Gr), which instead were assessed through opportunistic search efforts and camera trapping.

 

Habitat

Description

Surveys

No. of species, survey

Riverine forest (Rf)

Broadleaf forest and woodland along waterways.

9

24, 3

Wetland (We)

Open habitat, either permanently or seasonally saturated with water.

23

22, 3

Moorland (Mo)

Open habitat, characterised by low-growing vegetation on acidic soils.

8

16, 1

Broadleaf forest (Br)

Broadleaf forest and woodland.

22

22, 6

Bamboo forest (Bf)

Evergreen forest with bamboo as main vegetation type.

12

13, 4

Settlement (Se)

Villages and surroundings.

-

-

Grazing Land (Gr)

Grazing land and all other open areas except for wetland and moorland.

-

-

 

 

Table 3.Bird species identified within Sheka Forest Biosphere Reserve, with IUCN conservation status (LC: Least Concern, NT: Near Threatened, VU: Vulnerable, EN: Endangered, CR: Critically Endangered), predominant habitat occupation (see Table 2, Mi: Migration), the identification method leading to species detection (OO: opportunistic observation; PT: point count transect observation; CT: camera trap observation), and main verification method (PH: photographic recording; AU: audio recording; DO: double observation).  Species endemic to the Horn of Africa (Redman et al. 2011) are indicated with †.  Species that were only observed in the protected zones are indicated with ‡.  IUCN status according to https://www.iucnredlist.org, accessed on 29 September 2018.

 

 

Species/family

Common name

IUCN

Habitat

Identification

Verification

 

Podicipedidae (1)

 

 

 

 

 

1

Tachybaptus ruficollis

Little Grebe

LC

Rf, We

CT, OO, PT

PH

 

Phalacrocoracidae (1)

 

 

 

 

 

2

Phalacrocorax africanus

Long-tailed Cormorant

LC

Rf

OO, PT

DO

 

Anhingidae (1)

 

 

 

 

 

3

Anhinga rufa

African Darter

LC

Rf

OO, PT

PH

 

Heliornithidae (1)

 

 

 

 

 

4

Podica senegalensis

African Finfoot

LC

Rf

OO, PT

DO

 

Ardeidae (6)

 

 

 

 

 

5

Nycticorax nycticorax

Black-crowned Night Heron

LC

Rf

OO

DO

6

Bubulcus ibis

Cattle Egret

LC

Gr

OO, PT

DO

7

Ardeola ralloides

Squacco Heron

LC

Mi

OO

PH

8

Butorides striata

Striated Heron

LC

Rf

OO

DO

9

Ardea purpurea

Purple Heron

LC

Rf

OO, PT

DO

10

Ardea melanocephala

Black-headed Heron

LC

Rf, We

OO, PT

DO

 

Ciconiidae (5)

 

 

 

 

 

11

Ciconia ciconia

White Stork

LC

Mi

OO

DO

12

Ciconia microscelis

African Woollyneck

LC

Rf, We, Gr

OO, PT

PH

13

Ciconia abdimii

Abdim's Stork

LC

Gr, Se

OO

PH

14

Anastomus lamelligerus

African Openbill

LC

Mi

OO

PH

15

Leptoptilos crumeniferus

Marabou Stork

LC

We, Se

OO

PH

 

Threskiornithidae (2)

 

 

 

 

 

16

Bostrychia hagedash

Hadada Ibis

LC

We, Gr, Se

CT, OO, PT

PH

17

Bostrychia carunculata†

Wattled Ibis

LC

We, Gr

CT, OO, PT

PH

 

Anatidae (5)

 

 

 

 

 

18

Plectropterus gambensis‡

Spur-winged Goose

LC

We

OO

DO

19

Alopochen aegyptiaca

Egyptian Goose

LC

We, Rf

OO, PT

DO

20

Anas undulata

Yellow-billed Duck

LC

Rf

PT

PH

21

Anas sparsa

African Black Duck

LC

Rf

OO

PH

22

Anas crecca‡

Eurasian Teal

LC

Mi

OO

DO

 

Accipitridae (28)

 

 

 

 

 

23

Milvus migrans

Black Kite

LC

Gr, Se

OO, PT

PH

24

Milvus (migrans) aegyptius

Yellow-billed Kite

LC

Gr, Se

CT, OO, PT

PH

25

Haliaeetus vocifer

African Fish-Eagle

LC

Rf

OO, PT

PH

26

Necrosyrtes monachus

Hooded Vulture

CR

Gr, Se

CT, PT

PH

27

Trigonoceps occipitalis

White-headed Vulture

CR

Gr, Se

PT

PH

28

Torgos tracheliotus

Lappet-faced Vulture

EN

Gr, Se

OO

PH

29

Gyps africanus

White-backed Vulture

CR

Gr, Se

OO

PH

30

Gyps rueppellii

Rüppell’s Vulture

CR

Gr, Se

OO

PH

31

Circaetus cinereus‡

Brown Snake-Eagle

LC

Br

OO

PH

32

Circaetus pectoralis‡

Black-chested Snake-eagle

LC

Br

OO

PH

33

Accipiter tachiro

African Goshawk

LC

Br

OO, PT

PH

34

Accipiter rufiventris

Rufous-breasted Sparrowhawk

LC

Br

OO

PH

35

Accipiter minullus‡

Little Sparrowhawk

LC

Rf

OO

DO

36

Accipiter melanoleucus

Great Sparrowhawk

LC

Br

OO

PH

37

Aviceda cuculoides‡

African Cuckoo-Hawk

LC

Br

OO

PH

38

Polyboroides typus

African Harrier-Hawk

LC

Br, Gr, Se

OO, PT

PH

39

Pernis apivorus

European Honey-Buzzard

LC

Mi

OO

PH

40

Buteo augur

Augur Buzzard

LC

Gr, Br

OO, PT

PH

41

Buteo buteo

Common Buzzard

LC

Mi

OO, PT

PH

42

Buteo rufinus‡

Long-legged Buzzard

LC

Mi

OO

DO

43

Clanga pomarina‡

Lesser Spotted Eagle

LC

Mi

OO

PH

44

Aquila rapax

Tawny Eagle

LC

Gr

OO, PT

PH

45

Aquila nipalensis‡

Steppe Eagle

EN

Mi

OO

PH

46

Hieraaetus pennatus‡

Booted Eagle

LC

Mi

OO

DO

47

Hieraaetus ayresii

Ayres's Hawk-Eagle

LC

Br

OO

PH

48

Terathopius ecaudatus‡

Bateleur

NT

Gr

OO

PH

49

Lophaetus occipitalis

Long-crested Eagle

LC

Br, Gr

OO, PT

PH

50

Polemaetus bellicosus‡

Martial Eagle

VU

We

OO

PH

51

Stephanoaetus coronatus

African Crowned Eagle

NT

Br

OO

PH

 

Falconidae (3)

 

 

 

 

 

52

Falco ardosiaceus‡

Grey Kestrel

LC

Gr

OO

PH

53

Falco cuvierii‡

African Hobby

LC

Rf

OO

PH

54

Falco subbuteo‡

Eurasian Hobby

LC

Mi

OO

DO

 

Phasianidae (2)

 

 

 

 

 

55

Pternistis squamatus‡

Scaly Francolin

LC

Br

CT

PH

56

Pternistis castaneicollis†

Chestnut-naped Francolin

LC

Br, Gr

OO

AU

 

Sarothruridae (2)

 

 

 

 

 

57

Sarothrura elegans‡

Buff-spotted Flufftail

LC

Br

OO

AU

58

Sarothrura rufa‡

Red-chested Flufftail

LC

We

OO, PT

DO

 

Rallidae (4)

 

 

 

 

 

59

Amaurornis flavirostra

Black Crake

LC

Rf, We

OO, PT

PH

60

Rougetius rougetii†

Rouget’s Rail

NT

Rf, We, Mo

CT, OO, PT

PH

61

Rallus caerulescens

African Rail

LC

Rf, We

OO, PT

PH

62

Gallinula chloropus

Common Moorhen

LC

Rf

OO

DO

 

Gruidae (1)

 

 

 

 

 

63

Balearica pavonina

Black Crowned Crane

VU

We

OO

DO

 

Jacanidae (1)

 

 

 

 

 

64

Actophilornis africanus‡

African Jacana

LC

Rf

CT, OO

PH

 

Scolopacidae (4)

 

 

 

 

 

65

Actitis hypoleucos

Common Sandpiper

LC

Rf, We

OO

DO

66

Tringa glareola‡

Wood Sandpiper

LC

We

OO

DO

67

Tringa ochropus

Green Sandpiper

LC

We

OO

DO

68

Gallinago nigripennis‡

African Snipe

LC

We

PT

DO

 

Columbidae (10)

 

 

 

 

 

69

Treron calvus

African Green Pigeon

LC

Br

OO, PT

PH

70

Treron waalia

Bruce’s Pigeon

LC

Br

OO, PT

DO

71

Columba guinea

Speckled Pigeon

LC

Se

OO

DO

72

Columba arquatrix

African Olive Pigeon

LC

Br, Mo, Bf

OO, PT

PH

73

Turtur afer‡

Blue-spotted Wood Dove

LC

Br

OO, PT

DO

74

Turtur tympanistria

Tambourine Dove

LC

Br, Gr, Se

CT, PT

PH

75

Streptopelia vinacea

Vinaceous Dove

LC

Br, Gr

PT

DO

76

Streptopelia semitorquata

Red-eyed Dove

LC

Br, Gr, Se

OO, PT

PH

77

Streptopelia lugens ‡

Dusky Turtle Dove

LC

Br

PT

DO

78

Aplopelia larvata‡

Lemon Dove

LC

Br

CT, OO

PH

 

Psittacidae (2)

 

 

 

 

 

79

Poicephalus flavifrons†

Yellow-fronted Parrot

LC

Br

PT

PH

80

Agapornis taranta†

Black-winged Lovebird

LC

Br

PT

PH

 

Musophagidae (1)

 

 

 

 

 

81

Tauraco leucotis

White-cheeked Turaco

LC

Br, Bf

OO, PT

AU

 

Cuculidae (7)

 

 

 

 

 

82

Cuculus canorus

Common Cuckoo

LC

Mi

OO

DO

83

Cuculus solitarius

Red-chested Cuckoo

LC

Br, Se

OO, PT

PH

84

Cuculus clamosus

Black Cuckoo

LC

Br

PT

AU

85

Chrysococcyx klaas

Klaas’s Cuckoo

LC

Br, Se

OO, PT

AU

86

Chrysococcyx cupreus

African Emerald Cuckoo

LC

Br, Se

PT

PH

87

Centropus senegalensis

Senegal Coucal

LC

Br

CT, OO, PT

PH

88

Centropus monachus

Blue-headed Coucal

LC

Rf, We, Mo

OO, PT

PH

 

Strigidae (2)

 

 

 

 

 

89

Strix woodfordii

African Wood Owl

LC

Br

OO

AU

90

Bubo cinerascens

Greyish Eagle-Owl

LC

Br, Se

OO

DO

 

Apodidae (3)

 

 

 

 

 

91

Tachymarptis melba

Alpine Swift

LC

Mi

OO, PT

DO

92

Apus apus

Common Swift

LC

Gr, Se

OO, PT

DO

93

Apus niansae

Nyanza Swift

LC

Gr, Se

OO, PT

DO

 

Coliidae (1)

 

 

 

 

 

94

Colius striatus

Speckled Mousebird

LC

Se

CT, OO, PT

PH

 

Trogonidae (1)

 

 

 

 

 

95

Apaloderma narina

Narina Trogon

LC

Br

PT

AU

 

Alcedinidae (8)

 

 

 

 

 

96

Ceryle rudis

Pied Kingfisher

LC

Rf

OO, PT

PH

97

Megaceryle maxima

Giant Kingfisher

LC

Rf

PT

PH

98

Halcyon senegalensis

Woodland Kingfisher

LC

Rf, Br

PT

PH

99

Halcyon malimbica‡

Blue-breasted Kingfisher

LC

Rf

PT

PH

100

Halcyon chelicuti

Striped Kingfisher

LC

Br

OO

PH

101

Alcedo semitorquata‡

Half-collared Kingfisher

LC

Rf

OO, PT

PH

102

Corythornis cristatus

Malachite Kingfisher

LC

Rf

OO, PT

PH

103

Ispidina picta

Pygmy Kingfisher

LC

Rf, We

OO

PH

 

Meropidae (4)

 

 

 

 

 

104

Merops pusillus

Little Bee-eater

LC

Gr

OO

DO

105

Merops (variegatus) lafresnayii

Blue-breasted Bee-eater

LC

Br, Gr

OO

PH

106

Merops apiaster

European Bee-eater

LC

Gr

PT

DO

107

Merops albicollis

White-throated Bee-eater

LC

Rf, Br

PT

PH

 

Coraciidae (1)

 

 

 

 

 

108

Eurystomus glaucurus

Broad-billed Roller

LC

Rf

OO, PT

DO

 

Bucerotidae (1)

 

 

 

 

 

109

Tockus alboterminatus

Crowned Hornbill

LC

Br

OO, PT

AU

 

Bucorvidae (2)

 

 

 

 

 

110

Bycanistes brevis

Silvery-cheeked Hornbill

LC

Br

OO, PT

PH

111

Bucorvus abyssinicus

Abyssinian Ground-hornbill

LC

We, Gr

OO, PT

DO

 

Lybiidae (4)

 

 

 

 

 

112

Pogoniulus chrysoconus

Yellow-fronted Tinkerbird

LC

Br

OO, PT

PH

113

Pogoniulus pusillus

Red-fronted Tinkerbird

LC

Br

PT

AU

114

Lybius bidentatus

Double-toothed Barbet

LC

Br

OO

PH

115

Lybius undatus†

Banded Barbet

LC

Br

OO

DO

 

Indicatoridae (4)

 

 

 

 

 

116

Indicator indicator‡

Greater Honeyguide

LC

Rf

PT

PH

117

Indicator variegatus‡

Scaly-throated Honeyguide

LC

Rf

PT

AU

118

Indicator minor

Lesser Honeyguide

LC

Rf, Br

OO

AU

119

Prodotiscus zambesiae‡

Green-backed Honeybird

LC

Rf

OO

DO

 

Picidae (5)

 

 

 

 

 

120

Jynx torquilla

Eurasian Wryneck

LC

Mi

OO

DO

121

Campethera nubica

Nubian Woodpecker

LC

Br

PT

DO

122

Dendropicos fuscescens

Cardinal Woodpecker

LC

Br

OO, PT

PH

123

Dendropicos abyssinicus†

Abyssinian Woodpecker

LC

Br

PT

PH

124

Dendropicos spodocephalus

Grey-headed Woodpecker

LC

Gr

OO

DO

 

Hirundinidae (12)

 

 

 

 

 

125

Ptyonoprogne fuligula

Rock Martin

LC

Se

OO, PT

DO

126

Riparia paludicola schoensis

Plain Martin

LC

Gr

OO

DO

127

Delichon urbicum

Common House Martin

LC

Gr, Se

OO, PT

DO

128

Cecropis daurica

Red-rumped Swallow

LC

Gr, Se

OO, PT

DO

129

Cecropis senegalensis

Mosque Swallow

LC

Gr, Se

OO, PT

PH

130

Cecropis abyssinica

Lesser Striped Swallow

LC

Gr

OO

DO

131

Pseudhirundo griseopyga

Grey-rumped Swallow

LC

Mi

OO

DO

132

Hirundo rustica

Barn Swallow

LC

Gr, Se

OO, PT

DO

133

Hirundo lucida

Red-chested Swallow

LC

Gr

OO, PT

DO

134

Hirundo smithii

Wire-tailed Swallow

LC

Gr, Se

PT

PH

135

Hirundo aethiopica

Ethiopian Swallow

LC

Se

OO

DO

136

Psalidoprocne pristoptera

Black Saw-wing

LC

We, Gr, Se

OO, PT

PH

 

Motacillidae (9)

 

 

 

 

 

137

Motacilla flava (flava)

Yellow Wagtail

LC

Gr, Se

OO, PT

DO

138

Motacilla aguimp

African Pied Wagtail

LC

Rf

CT, OO, PT

PH

139

Motacilla clara

Mountain Wagtail

LC

Rf

OO, PT

PH

140

Motacilla alba

White Wagtail

LC

Mi

OO

DO

141

Anthus cinnamomeus

Grassland Pipit

LC

We, Gr

CT, OO

PH

142

Anthus leucophrys omoensis

Plain-backed Pipit

LC

Gr

OO

PH

143

Anthus similis

Long-billed Pipit

LC

Gr

OO

PH

144

Anthus cervinus

Red-throated Pipit

LC

Mi

PT

PH

145

Anthus trivialis

Tree Pipit

LC

Mi

OO

DO

 

Campephagidae (2)

 

 

 

 

 

146

Campephaga phoenicea

Red-shouldered Cuckooshrike

LC

Br

PT

PH

147

Coracina caesia

Grey Cuckooshrike

LC

Rf, Br

OO

DO

 

Pycnonotidae (2)

 

 

 

 

 

148

Pycnonotus barbatus schoanus

Common Bulbul

LC

Br, Mo, Gr, Se

CT, OO, PT

PH

149

Atimastillas flavicollis

Yellow-throated Leaflove

LC

Br

PT

DO

 

Muscicapidae (20)

 

 

 

 

 

150

Cossypha semirufa

Rüppell's Robin-Chat

LC

Br, Bf, Gr, Se

CT, OO, PT

PH

151

Cossypha heuglini

White-browed Robin-Chat

LC

Rf

OO

DO

152

Phoenicurus phoenicurus

Common Redstart

LC

Mi

OO, PT

DO

153

Saxicola (torquatus) albofasciatus

African Stonechat

LC

We, Gr

OO, PT

PH

154

Saxicola rubetra

Whinchat

LC

We, Gr

OO, PT

DO

155

Oenanthe oenanthe

Northern Wheatear

LC

Mi

OO

PH

156

Cercomela sordida

Moorland Chat

LC

We, Mo, Se

OO, PT

PH

157

Psophocichla litsitsirupa

Groundscraper Thrush

LC

Se

OO, PT

PH

158

Monticola saxatilis

Common Rock Thrush

LC

Mi

OO, PT

DO

159

Turdus (olivaceus) abyssinicus

African Mountain Thrush

LC

Br, Bf, Gr, Se

CT, PT

PH

160

Turdus pelios

African Thrush

LC

Gr, Se

OO

DO

161

Zoothera piaggiae

Abyssinian Ground Thrush

LC

Br

CT, PT

PH

162

Melaenornis chocolatinus†

Abyssinian Slaty Flycatcher

LC

Br, Gr, Se

OO, PT

PH

163

Melaenornis edolioides

Northern Black Flycatcher

LC

Gr, Se

OO

PH

164

Bradornis microrhynchus

African Grey Flycatcher

LC

Br

OO

DO

165

Bradornis pallidus

Pale Flycatcher

LC

Se

OO

DO

166

Muscicapa adusta

African Dusky Flycatcher

LC

Br, Mo, Bf, Se

PT

PH

167

Muscicapa striata

Spotted Flycatcher

LC

Mi

OO

DO

168

Terpsiphone viridis

African Paradise Flycatcher

LC

Br, Gr, Se

CT, OO, PT

PH

169

Myioparus plumbeus

Lead-coloured Flycatcher

LC

Br

PT

PH

 

Locustellidae (6)

 

 

 

 

 

170

Bradypterus baboecala

Little Rush Warbler

LC

Rf, We

OO, PT

AU

171

Bradypterus cinnamomeus

Cinnamon Bracken Warbler

LC

Br, Mo, Bf

PT

PH

172

Bradypterus alfredi‡

Bamboo Warbler

LC

Bf

OO, PT

AU

173

Acrocephalus baeticatus‡

African Reed Warbler

LC

Rf

OO, PT

AU

174

Acrocephalus schoenobaenus‡

Sedge Warbler

LC

Mi

OO

DO

175

Chloropeta natalensis

African Yellow Warbler

LC

We, Gr

PT

PH

 

Cisticolidae (8)

 

 

 

 

 

176

Camaroptera brevicaudata

Grey-backed Camaroptera

LC

Br, Mo

OO, PT

AU

177

Eremomela canescens‡

Green-backed Eremomela

LC

Br

OO

DO

178

Cisticola (galactotes) lugubris†

Ethiopian Cisticola

LC

Rf, We, Mo

OO, PT

PH

179

Cisticola erythrops

Red-faced Cisticola

LC

Rf

OO

DO

180

Cisticola cantans

Singing Cisticola

LC

Gr, Se

PT

DO

181

Prinia subflava

Tawny-flanked Prinia

LC

Gr, Se

PT

PH

182

Apalis flavida

Yellow-breasted Apalis

LC

Br, Gr, Se

PT

DO

 

Phylloscopidae (3)

 

 

 

 

 

183

Phylloscopus trochilus

Willow Warbler

LC

Br, Gr, Se

OO, PT

DO

184

Phylloscopus collybita

Common Chiffchaff

LC

Br, Gr, Se

OO, PT

AU

185

Phylloscopus umbrovirens

Brown Woodland Warbler

LC

Br, Mo, Bf

OO, PT

PH

 

Sylviidae (5)

 

 

 

 

 

186

Sylvia atricapilla

Blackcap

LC

Br, Gr, Se

OO, PT

PH

187

Sylvia borin‡

Garden Warbler

LC

Mi

OO, PT

AU

188

Sylvia abyssinica

African Hill Babbler

LC

Br, Mo

OO, PT

PH

189

Turdoides leucopygia

White-rumped Babbler

LC

Br

OO, PT

PH

190

Parophasma galinieri†‡

Abyssinian Catbird

LC

Mo, Bf

OO, PT

AU

 

Platysteiridae (2)

 

 

 

 

 

191

Batis erlangeri

Western Black-headed Batis

LC

Br

PT

AU

192

Platysteira cyanea

Brown-throated Wattle-eye

LC

Br

OO, PT

AU

 

Zosteropidae (2)

 

 

 

 

 

193

Zosterops poliogastrus kaffensis

Montane White-eye

LC

Br, Bf

OO, PT

DO

194

Zosterops abyssinicus

Abyssinian White-eye

LC

Br

OO, PT

DO

 

Nectariniidae (6)

 

 

 

 

 

195

Nectarinia tacazze

Tacazze Sunbird

LC

Br, Mo, Gr, Se

OO, PT

PH

196

Cinnyris cupreus

Copper Sunbird

LC

Br, Gr, Se

OO, PT

DO

197

Cinnyris venustus fazoqlensis

Variable Sunbird

LC

Br, Gr, Se

PT

PH

198

Cinnyris chloropygius

Olive-bellied sunbird

LC

Rf

OO

DO

199

Chalcomitra senegalensis

Scarlet-chested Sunbird

LC

Br

PT

AU

200

Cyanomitra olivacea ragazzii

Olive Sunbird

LC

We, Br, Gr

PT

PH

 

Laniidae (3)

 

 

 

 

 

201

Lanius humeralis

Northern Fiscal

LC

We, Gr, Se

PT

PH

202

Lanius excubitor leucopygos

Great Grey Shrike

LC

Mi

OO

DO

203

Lanius collurio/isabellinus‡

Red-backed/Isabelline Shrike

LC

Mi

PT

DO

 

Malaconotidae (3)

 

 

 

 

 

204

Laniarius aethiopicus

Ethiopian Boubou

LC

Br, Gr, Se

CT, OO, PT

PH

205

Dryoscopus cubla

Northern Puffback

LC

Br, Gr, Se

OO, PT

AU

206

Tchagra senegalus

Black-crowned Tchagra

LC

Br

OO

DO

 

Oriolidae (3)

 

 

 

 

 

207

Oriolus oriolus‡

Eurasian Oriole

LC

Mi

OO, PT

PH

208

Oriolus larvatus rolleti

Black-headed Oriole

LC

Br

OO, PT

DO

209

Oriolus monacha†

Abyssinian Oriole

LC

Br, Bf

OO, PT

PH

 

Corvidae (3)

 

 

 

 

 

210

Corvus capensis

Cape Crow

LC

Se

OO, PT

PH

211

Corvus rhipidurus

Fan-tailed Raven

LC

Se

OO

PH

212

Corvus crassirostris†

Thick-billed Raven

LC

Gr, Se

CT, OO, PT

PH

 

Buphagidae (1)

 

 

 

 

 

213

Buphagus erythrorynchus

Red-billed Oxpecker

LC

Gr

OO

PH

 

Sturnidae (8)

 

 

 

 

 

214

Poeoptera stuhlmanni

Stuhlmann's Starling

LC

Br

OO, PT

PH

215

Onychognathus morio

Red-winged Starling

LC

Br

OO

DO

216

Onychognathus tenuirostris

Slender-billed Starling

LC

Br, Gr

PT

DO

217

Lamprotornis chalybaeus

Greater Blue-eared Starling

LC

Br, Gr, Se

OO, PT

PH

218

Lamprotornis splendidus‡

Splendid Starling

LC

Rf, Br

OO, PT

DO

219

Lamprotornis purpuroptera

Rüppell's Starling

LC

Rf

OO, PT

AU

220

Pholia sharpii

Sharpe's Starling

LC

Br, Bf

OO, PT

PH

 

Passeridae (1)

 

 

 

 

 

221

Passer swainsonii

Swainson's Sparrow

LC

Gr, Se

OO, PT

PH

 

Ploceidae (7)

 

 

 

 

 

222

Ploceus cucullatus abyssinicus

Village Weaver

LC

Se

OO, PT

DO

223

Ploceus ocularis

Spectacled Weaver

LC

Br, Gr, Se

OO, PT

DO

224

Ploceus nigricollis

Black-necked Weaver

LC

Br

OO

PH

225

Ploceus baglafecht

Baglafecht Weaver

LC

Br, Gr, Se

OO, PT

DO

226

Amblyospiza albifrons‡

Grosbeak Weaver

LC

Rf, We

PT

PH

227

Anaplectes rubriceps

Red-headed Weaver

LC

Br

OO

DO

 

Viduidae (5)

 

 

 

 

 

228

Anomalospiza imberbis‡

Cuckoo Finch

LC

Rf, We

OO

DO

229

Euplectes axillaris‡

Fan-tailed Widowbird

LC

Rf, We

PT

DO

230

Euplectes albonotatus‡

White-winged Widowbird

LC

Rf, We

PT

DO

231

Vidua macroura

Pin-tailed Whydah

LC

Gr, Se

OO

DO

232

Vidua chalybeata

Village Indigobird

LC

Gr, Se

OO

PH

 

Estrildidae (8)

 

 

 

 

 

233

Mandingoa nitidula

Green Twinspot

LC

Br

OO

DO

234

Cryptospiza salvadorii

Abyssinian Crimsonwing

LC

Br, Bf

PT

AU

235

Lagonosticta senegala

Red-billed Firefinch

LC

Gr, Se

OO, PT

PH

236

Coccopygia quartinia

Yellow-bellied Waxbill

LC

Br, Gr, Se

OO, PT

PH

237

Estrilda astrild peasei

Common Waxbill

LC

Gr, Se

CT, OO, PT

PH

238

Estrilda (Paludicola) ochrogaster

Abyssinian Waxbill

LC

Gr, Se

OO, PT

DO

239

Lonchura cucullata

Bronze Mannikin

LC

Gr, Se

OO

DO

240

Spermestes bicolor poensis

Black-and-white Mannikin

LC

Br, Gr

PT

PH

 

Fringillidae (4)

 

 

 

 

 

241

Serinus mozambicus

Yellow-fronted Canary

LC

Gr

OO

DO

242

Serinus citrinelloides

African Citril

LC

Gr, Se

OO, PT

PH

243

Serinus tristriatus

Brown-rumped Seedeater

LC

Gr, Se

OO, PT

PH

244

Serinus striolatus

Streaky Seedeater

LC

Gr, Se

PT

PH

 

 

For figure & images – click here

 

 

References

 

Aerts, R., G. Berecha & O. Honnay (2015). Protecting coffee from intensification. Science 347: 139.

BirdLife International (2017). The World Database of Key Biodiversity Areas. Key Biodiversity Areas Partnership: BirdLife International, IUCN, Amphibian Survival Alliance, Conservation International, Critical Ecosystem Partnership Fund, Global Environment Facility, Global Wildlife Conservation, NatureServe, Royal Society for the Protection of Birds, World Wildlife Fund and Wildlife Conservation Society. Downloaded from http://www.keybiodiversityareas.org on 02 November 2017.

De Beenhouwer, M., R. Aerts & O. Honnay (2013). A global meta-analysis of the biodiversity and ecosystem service benefits of coffee and cacao agroforestry. Agriculture, Ecosystems & Environment 175: 1–7.

Dessie, G. & J. Kleman (2007). Pattern and magnitude of deforestation in the South Central Rift Valley Region of Ethiopia. Mountain Research and Development 27: 162–168.

Engelen, D., D. Lemessa, Ç.H. Şekercio Ğlu & K. Hylander (2017). Similar bird communities in homegardens at different distances from Afromontane forests. Bird Conservation International 27: 83–95.

FAO (2015). Global Forest Resources Assessment 2015. Food and Agriculture Organization of the United Nations, Rome, 244pp.

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