
==== Front
BMC Zool
BMC Zool
BMC Zoology
2056-3132
BioMed Central London

215
10.1186/s40850-024-00215-x
Research
Assessment of bird diversity and abundance in Mai-Nigus artificial reservoir and surrounding semi-forest in Tigray Region, Northern Ethiopia
Assefa Alembrhan assefaw12@gmail.com

1
Mesfin Kalayu 1
Tesfahunegny Weldemariam 2
Fitsum Birkti 3
Gaim Amleset 1
Meles Teklay 1
1 https://ror.org/003659f07 grid.448640.a 0000 0004 0514 3385 Department of Biology, College of Natural and Computational Science, Aksum University, P.O. Box, 1010, Axum, Tigray Ethiopia
2 https://ror.org/05rvzq326 grid.512246.6 0000 0004 9474 6304 Ethiopian Biodiversity Institute, Mekelle Biodiversity Center, P. O. Box, 30726, Mekelle, Tigray Ethiopia
3 https://ror.org/003659f07 grid.448640.a 0000 0004 0514 3385 Department of Geography and Environmental Studies, College of Social Science and Languages, Aksum University, P.O. Box, 1010, Axum, Tigray Ethiopia
14 9 2024
14 9 2024
2024
9 2423 4 2024
4 9 2024
© The Author(s) 2024
2024
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Background

Artificial reservoirs are alternative habitats for bird diversity, and knowledge of the diversity and abundance of bird species contribute to the management of the ecosystem. This study was conducted to investigate the species diversity and abundance of birds in Mai-Nigus reservoir and its surrounding semi-forest from July 2022 to March 2023. Point count method with a total of fifteen count stations at an interval of 50 m radius was used to study the diversity and abundance of bird species in the semi-forest habitat while total count employed on the reservoir.

Results

A total of 123 bird species comprising endemic and globally threatened species were identified. Order Passeriformes had the highest number of species followed by Charadriiformes and Pelecaniformes. Family Scolopacidae was the most abundant followed by Ardeidae, Ploceidae and Anatidae. Bird species richness and abundance were not significantly varied across seasons and habitats (P > 0.05). The highest species diversity (H´=3.96) were recorded in the Semi-forest during the wet season, whereas the least was recorded from reservoir during the dry season (H´=2.66). The highest and lowest species evenness of birds was recorded in Semi-forest (E = 0.725) and reservoir (E = 0.448) during the dry season, respectively. Most birds that inhabited the area had frequent relative abundance followed by uncommon and common species.

Conclusion

Mai-Nigus reservoir and surrounding habitat host high bird diversity and this requires critical conservation concerns for the long-term survival of birds.

Supplementary Information

The online version contains supplementary material available at 10.1186/s40850-024-00215-x.

Keywords

Anthropogenic threat
Artificial reservoir
Diversity
Indicator bird
Waterbirds
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pmcBackground

Ethiopia is one of the African countries comprising the highest diversity of living organisms with high level of endemism [1–3]. The diverse habitat types, altitudinal ranges, climatic conditions and soil types contribute the country hosting enormously diverse bird species [3, 4]. About 881 species of birds have been enumerated from Ethiopia, of which 18 species are endemic to the country and 10 species are shared with Eritrea [4–6]. The government of Ethiopia has identified 73 important bird areas to conserve various terrestrial and aquatic birds as well as other organisms [7, 8].

Birds are critical components of the ecosystem due to their roles in various ecological functions, including pollination, seed dispersal, pest control, energy flow and nutrient cycling [9–11]. Avian diversity is often used as an indicator of overall biodiversity and ecosystem health [10]. Besides, they are used as source of food, sources of spiritual and artistic inspirations and source of tourist attractions due to their distinctive body structure, colour, calls, songs and other activities such as courtship display [12–14]. Birds are among the best studies elements of the earth’s biodiversity; however quantified information of birds in Ethiopia is still in its infancy due to lack of trained professionals and this leads to an obstacle in conservation [15–17]. Patterns of distribution and abundance of birds are strongly related to environmental factors, which determine their occurrence and activity [15]. Bird species diversity, abundance and distribution are highly influenced by seasonality as season affects the availability of food and cover of birds, which in turn affects their breeding success and survival [18, 19]. Globally, biodiversity has been changed due to habitat destruction and modification and these factors are identified as major causes of large-scale declines in several species of wildlife including bird fauna [15, 20, 21].

Despite the rich bird assemblages in Ethiopia, survivals of endangered bird species is lying on thin line due to various threats such as habitat fragmentation, degradation and loss [15, 22]. Mostly, agricultural land expansion, livestock encroachment, deforestation, indiscriminate fire and others have been identified as the major cause of birds’ habitat degradation, fragmentation and loss in Ethiopia ultimately affecting the survival of birds [20, 23]. Now a day, high numbers of bird species inhabit newly formed unprotected habitat types such as reservoirs and urban areas out of their natural habitats [24–26]. In Ethiopia many reservoirs have been constructed for irrigation, fishing, hydropower, livestock drinking, washing and other human uses [24, 27]. In addition, artificial reservoirs are also considered as alternative promising sites for the breeding, feeding and nesting of several aquatic birds [27, 28]. Most of the previous studies on birds of the country were focused on the forest birds [8, 14]. However, studies conducted on aquatic birds in artificial reservoirs are few in number, which are sporadic and disjointed in nature [28–30]. Hence, this shows that in Ethiopia’s bird diversity in artificial reservoirs has been mistreated compared to the protected areas and the reason for this could be the lack of scientific data on the diversity and abundance of waterbirds therein.

Particularly, above 80 reservoirs have been made since 1990s to combat drought in Ethiopia’s Tigray region. Studies by Kiros et al. [15] and Tsehaye et al. [27] revealed that artificial reservoirs of the region exhibit a peculiar biodiversity in waterbirds. However, this exploration was not extended to all artificial reservoirs of the region [15]. Bird diversity of the reservoirs located in central and northwestern zones has not yet been explored and this is true for the Mai-Nigus reservoir which is found in the central zone of Tigray. Hence, in newly created habitats like the Mai-Nigus artificial reservoir, studying avian diversity can provide valuable insights into the ecological processes of colonization, adaptation, and community structure development. It also helps to test the diversity and complexity of habitats around the Mai-Nigus artificial reservoir significantly contribute to higher avian species richness and abundance compared to surrounding terrestrial areas. Therefore, the study was aimed to assess information on the bird diversity and abundance of the Mai-Nigus artificial reservoir and its adjoining habitat for better understanding of the habitat suitability for birds and subsequently for future protection and management of such vital area.

Materials and methods

Description of the study area

This particular study was conducted in Mai-Nigus reservoir and its adjoining habitat found in the central zone at Laelay-maychew district particularly in Dura village of Tigray region, northern Ethiopia. The reservoir is located at 14° 11’ 76” N latitude and 39° 16’ 01” E longitude (Fig. 1). It is found nearby (~ 6 km west) to the ancient historical town of Axum, and at 251 km and 1006 km far away from Mekelle city, the capital city of Tigray region and Addis Ababa, the capital city of Ethiopia, respectively. The average altitude of the reservoir is 2,056 m above sea level (m.a.s.l) with an average temperature of 20.6 °C [31]. Its mean annual rainfall is 663 mm, and the pattern of its rainfall distribution is uni-modal, which mostly occurs from June to September. Mai-Nigus reservoir is an engineered aquatic habitat designed primarily for water storage and irrigation purposes with a total area of 40 hectares [27]. Constructed to address water scarcity issues and enhance agricultural productivity, the reservoir has inadvertently created a new ecosystem that supports a diverse range of flora and fauna such as phytoplankton, zooplankton, fish and fish-eating avian species [27]. The surrounding habitats, comprising a mix of semi-forest including church forest, human settlement, and agricultural fields, further contribute to the ecological complexity of the area. The reservoir is highly interfered with human activities like irrigation and livestock drinking mainly during the dry season.

Fig. 1 Map of the study area

Bird survey

A preliminary survey was carried out in the first week of July 2022 in the study area, to gather baseline information like topographic features, habitat types and bird status. This led to the selection of two habitat types – the reservoir and the adjoining semi-forest for the study (Fig. 2). Based on the habitat type and suitability, total count and point transect techniques were employed to study birds [15, 32, 33]. In the semi-forest habitat type point count method, which is a systematic exploration in a fixed area and time interval was used [34]. During the point count method, fifteen point count stations or observation points were established systematically and birds were identified and counted from a fixed position within a 50 m radius for a specific period of 15 min at every point [35]. All birds seen or heard within this 50 m radius were recorded [34]. To minimize the double counting problem, point stations were intentionally set at a distance of 50 m intervals [20]. Due to the inaccessibility of implementing the point count technique, a total count technique was employed to study birds in the reservoir [15]. Total count was used wherever possible by walking around the proximate areas or from specific vantage points to count birds. Birds on the open water were counted by moving to all directions of the reservoir. However, birds crossing the middle of the reservoir were identified and counted on their destination sides. In both habitats, a waiting period of five minutes was made to reduce disturbance and then identification and counting was carried out for 15 min [28].Fig. 2 Habitat types selected for the present study: reservoir (left) and semi-forest (right) photo by Alembrhan A

Field data collection was conducted from July to October 2022 (wet season) and from January to March 2023 (dry season). Birds were identified and counted three days per month twice a day in the early morning (6:00–10:00 AM) and in the late afternoon (4:00–6:00 PM) when the bird activity was peak [20] using binocular (10 × 50). Appropriate coloured field guides were used to identify birds to their species level [36, 37]. Moreover, photographs were also taken to identify the birds that were not easily identified in the field by checking with the field guides. GPS reading were employed to locate the bird counting points and record the locations of the study area.

Data analysis

Data were analyzed using the PAST software, version 3.26 and Microsoft Excel program. PAST software [38] was used to calculate Shannon-Wiener diversity index (H’). Evenness index (E) was used to calculate the species evenness of birds [39]. Simpson’s similarity index (SI) was used to evaluate the similarity between habitat types in terms of their species composition and its was calculated using this formula; SI=2CA+B where, A is the number of bird species that found in site A, B is the number of species in site B, and C is the number of common species in sites A and B [40]. Relative abundance (RA) of bird species was determined as the ratio between the number of individuals counted for a species and the total number of individuals of all species counted in percentage. R\%=nN x 100, where n is the number of individuals counted for a species and N is the total number of individuals of all species counted during the study period [25]. The relative abundance rank of bird species was computed using the number of individual birds of a species counted in a given area per day. For instance a species numbering 201 to 1000 individuals per day is categorized under abundant, 51 to 200 is very common, 21 to 50 is common, 7 to 20 is Frequent, 1 to 6 is uncommon and a species with 1 to 6 individuals per season is rare [41, 42]. Kolmogorov-Smirnov test was used to test the data normality and then Two-way ANOVA was used to test the significant variation of bird species richness and abundance between habitat types and seasons.

Results

Species composition of birds

A total of 123 bird species belonging to 15 orders, 42 families and 84 genera were recorded during the study period (Appendix 1). From all the identified bird species, Order Passeriformes (35%) had the highest number of species followed by order Charadriiformes (17.1%) and order Pelecaniformes (11.4%), respectively. The majority of bird species are of the family Scolopacidae (12 species) followed by Ardeidae (9 species) and Ploceidae and Anatidae (8 species for each). Of the bird species recorded 3 species were endemic to Ethiopia; Wattled Ibis (Bostrychia carunculata), Abyssinian Catbird (Parophasma galinieri) and Abyssinian Woodpecker (Dendropicos abyssinicus) and three species were near-endemic (endemic to Ethiopia and Eritrea) include Rouget’s Rail (Rougetius rougetii), White-winged Cliff-chat (Thamnolaeasemirufa) and Black-winged Lovebird (Agapornis taranta) (Appendix 1). In addition, one vulnerable species, the Abyssinian Ground-Hornbill (Bucorvus abyssinicus) and three near-threatened species such as Rouget’s Rail (Rougetius rougetii), Eurasian Curlew (Numenius arquata) and Great Snipe (Gallinago media) were also recorded. Out of the total 123 bird species recorded, 87 species were recorded during the wet season and 58 species were recorded during the dry season. Among these 22 species were observed during both seasons, 65 species only during the wet season and 36 species were recorded only during dry the season.

Distribution and abundance of birds

In this study, species distribution was varied between habitat types during the wet and dry seasons (Table 2). From the total bird species recorded, 70 species were recorded in the reservoir and 113 species in the semi-forest. Of these, 10 species were recorded in the reservoir and 53 species were recorded in the semi-forest. Sixty bird species were recorded in both habitat types. Moreover, 51 and 32 species were recorded in the reservoir, and 72 and 51 species were recorded in the semi-forest during the wet and dry season, respectively. During the study period, a total of 3,572 individual birds were counted, of which 1,921 individuals were recorded during the wet season and 1,651 individuals were recorded during the dry season. The higher number of bird abundance was recorded in the reservoir habitat of 1,852 individuals, while the lower was recorded in the semi-forest habitat of 1,720 individuals. Based on the ANOVA analysis, there was no significant difference in number of bird species and abundance across seasons and habitat types (P > 0.05). Abundance score and ordinal scale of birds estimated by encounter rate showed that most bird species, 22 species were found within the ordinal rank of “frequent” during the wet season on the reservoir and 34 species within “uncommon” during the wet season on the semi-forest habitat. Least number of birds was recorded as “very common” and “abundant” (n = 1 species for each) during the wet and dry seasons from reservoir habitat (Table 1). From the total 123 species recorded, Egyptian goose (Alopochen aegyptiaca) accounted the highest relative abundance (12.7%) followed by Spur-winged lapwing (Vanellus spinosus) (4.54%) and Ruff (Calidris pugnax) (4.34%), whereas Greater spotted eagle (Clanga clanga) and Double-toothed barbet (Lybius bidentatus) were with the least relative abundance (Appendix 1).

Table 1 Relative abundance rank of birds in Mai-Nigus reservoir during the wet and dry seasons

Habitat type	Season	Rank	
		Rare	Uncommon	Frequent	Common	Very Common	Abundant	
Reservoir	Wet	7	15	22	6	1	–	
	Dry	3	6	14	8	–	1	
Semi-forest	Wet	6	34	32	7	–	–	
	Dry	7	14	27	3	–	–	

Bird species diversity and evenness

Bird species diversity was higher during the wet season in both habitats compared to the dry season. The highest diversity of bird species was recorded in the semi-forest habitat (H’ = 3.96) during the wet season while the lowest diversity of species was found in the reservoir (H’ = 2.66) during the dry season (Table 2). Across both seasons, higher values of Shannon’s diversity index was recorded in the semi-forest (H’ = 4.28) than in the reservoir (H’ = 3.40). The highest species evenness was found in the semi-forest habitat during the dry season (E = 0.725) and wet season (E = 0.665). Between both seasons, the higher species evenness was recorded from the semi-forest (E = 0.637) than reservoir (E = 0.427) (Table 2).

Table 2 Bird species diversity between two habitats during wet and dry seasons

Habitat type	Season	No. of species	Abundance	H´	E	
Reservoir	Wet	51	887	3.46	0.625	
	Dry	32	965	2.66	0.448	
	Both	70	1,852	3.40	0.427	
Semi-forest	Wet	79	1,034	3.96	0.665	
	Dry	51	686	3.61	0.725	
	Both	113	1,720	4.28	0.637	
Where H´ Shannon-Wiener diversity Index, E Evenness

Bird species similarity index

Among 87 species which were recorded during the wet season, 79 and 51 species were recorded in the semi-forest and reservoir habitats, respectively. Forty three species were common to both habitats. A total 58 species were also recorded during the dry season. Among them 51 species were found in the semi-forest, 32 species on the reservoir and 25 species were common to both habitats. The similarity index of bird species between two habitats showed variations between wet and dry seasons. Accordingly, more species similarly was observed during the wet season in the reservoir and semi-forest (SI = 0.662) while the least similarity was observed between the two habitats during the dry season (SI = 0.602) (Table 3). The overall bird community similarity of the reservoir and semi-forest habitats was SI = 0.656, which is > 50%, and this indicated that there is high similarity of bird species between these two habitats.

Table 3 Bird species similarity between two habitat types during wet and dry seasons

Habitat type	Simpson’s similarity index (SI)	
Season	Reservoir	Semi-forest	
Reservoir	Wet	-	0.662	
	Dry	-	0.602	
	Both	-	0.656	
Semi-forest	Wet	0.662	-	
	Dry	0.602	-	
	Both	0.656		

Discussion

High avian species (123) consisting endemic and globally threatened species were recorded in the study area. This proved that the Mai-Nigus reservoir and its adjoining habitat are very crucial for bird conservation. An area with sufficient food sources and diverse vegetation structure or the presence of diverse habitats supports variety of bird species [43, 44]. The observed richness of birds in the area might be due to the availability of numerous aquatic organisms such as fishes, snails, amphibians, aquatic insects and vegetation structures in and around the reservoir that provide wide range of foraging, roosting and nesting sites for the birds. However, the number of bird species of the area might be above the recorded ones this might due to different limitations of the present study such as survey duration, anthropogenic factors and ecological data gaps.

Out of the total bird species recorded six species; Wattled Ibis (Bostrychia carunculata), Rouget’s Rail (Rougetius rougetii), Abyssinian Catbird (Parophasma galinieri), Black-winged Lovebird (Agapornis taranta), Abyssinian Woodpecker (Dendropicos abyssinicus) and White-winged Cliff-chat (Thamnolaea semirufa) are endemic to Ethiopia and shared with the neighbor country Eritrea. This is accordance with findings of several authors who reported many endemic and near-endemic species in different areas of Ethiopia [45–47]. The presence of high number of near-endemic bird species in the area might be due to its proximity to Eritrea (~ 60 km) and similarity in ecological and climatic conditions.

In the present study higher bird species richness and abundance were recorded during the wet season than during the dry season. This variation could be the availability of various food sources, habitat conditions and birds breeding season. For example in relation to heavy rainfall aids in production of insects and fishes that are used as food sources for birds which mainly happen during the wet season [48]. The finding of this study is in accordance with the idea that bird species richness and abundance are influenced by local resources and vegetation composition [45]. Besides, during the wet season the productivity and yield of habitats increase as many of the invertebrates and fishes breed and the herbs become more productive on which the birds depend; as a result, the richness and abundance of birds increase [47]. However, this is in contrast to the findings of various authors who reported that the species richness and abundance of bird species was higher during the dry season due to availability high food items such as fruits and flowering plants in the area [29, 30, 46].

The semi-forest habitat had high bird species richness. This might be due to the presence of wide array of vegetation types that provide different habitat types for many bird species as well as its wide area might contribute to inhabit by diverse bird species. In contrast, the reservoir had high bird abundance. This could be related with high productivity of the reservoir habitat and associated characteristics. The availability of food materials, high productivity level, adequate shelter and breeding habitats are important factors that determine the bird species richness and abundance of an area [49].

Abundance score and ordinal scale of birds revealed that most bird species of the study area found within the ordinal rank of “frequent”. The possible reasons for this could be the availability of food sources, visibility of birds in the reservoir, quality of the reservoir and the surrounding habitat to harbor high number of individuals of a species. This finding agrees to Ayalew et al. [33] and Yenew and Dessalegn [46] who reported more frequent bird species. However, this finding is contrary to other authors who reported more rare species [28], common species [30] and uncommon species [47, 50]. Based on their reasons, the occurrence of more rare and uncommon species of birds may be related with their behavior and habitat condition. Breeding habitat, wide home range, niche of a species and habitat degradation are the main factors which lead to the presence of uncommon birds in a given area [51]. From the total bird species recorded, Egyptian Goose (Alopochen aegyptiaca) was the most abundant species. This might be related with its ability to inhabit and feed in both terrestrial and aquatic habitats. This finding concurs with many authors who reported high abundance of the species from localities of the country [15, 24, 28]. The occurrence of relatively high number of Pink-backed Pelican (Pelecanus rufescens) and Great White Pelican (Pelecanus onocrotalus) in this study indicates the presence of fishes in the reservoir and it can also be due to their piscivore diet.

The diversity index result indicated that the highest diversity and evenness of bird species were recorded in the semi-forest habitat during both wet and dry seasons. The species diversity increased during the wet season in both habitats that the dry season. This could be due to the presence of large number of individuals of Egyptian goose during the dry season which affects the Shannon-Weiner diversity index calculation. In addition, complex habitat types may support high number of species compared to habitat types with simple structure, since there are more niches delivering various types of nesting and feeding resources. This finding contradicts to Alemayehu and Dereje [28] who reported that bird species diversity and species evenness were higher in dam than its surrounding habitat. Moreover, Amare and Girma [21] also reported the highest birds’ species diversity and species evenness in Lake Hawasa unlike to adjoining habitats. Bird species similarity analysis between the reservoir and semi-forest habitat types showed that more species similarity was observed during the wet season while the least similarity was observed between the two habitats during the dry season. This is in accordance with authors who recorded that higher similarity of bird species observed between two habitats during the wet season than during the dry season [33, 47]. In this study, the overall bird species similarity between reservoir and semi-forest was high. This high similarity of bird species between the two habitats could be attributed to the existence of the semi-forest habitat close to the reservoir. Closed habitats can share similar species since they are geographically close which allows individuals to move from one habitat to another easily.

Although the reservoir and its surrounding harbor high bird species, it is highly threatened by various anthropogenic factors include irrigation, overgrazing, agricultural encroachment, unregulated use of agrochemicals, human settlement and land degradation. The regional government constructed the reservoir mainly for irrigation purpose; as a result, farmers extensively use water for irrigation and livestock drinking during the dry season. This leads in the reservoir, specifically to late March, water level falls and most of the birds move from the reservoir to elsewhere and this may be the possible reason for less species richness during the dry season.

Conclusion

The research result confirmed that there are 123 species of birds in the area among which 6 are endemic and near endemic to Ethiopia and 4 are globally threatened species. The presence of high number of species suggests that Mai-Nigus artificial reservoir and its adjoining semi-forest habitat are important conservation areas of birds. The highest species richness was recorded in semi-forest habitat while the highest abundance in reservoir. This indicates that both habitats provide the necessary requirements such as food, water, nesting and breeding sites to birds. Despite the fact that the reservoir and its surrounding habitat are home to numerous bird populations, high human pressure from the surrounding area with intensive irrigation, agricultural expansion, livestock grazing and settlement are putting pressure and becoming major threats of the birds and their habitat. Therefore, implementing long-term monitoring plans by engaging local communities to mitigate the human impacts, and restoring such habitats for the protection of bird species are crucial steps for the effective conservation of avian diversity in this important ecological area.

Supplementary Information

Supplementary Material 1.

Appendix

Table 4 Bird species and their abundance in Mai-Nigus reservoir during wet and dry seasons

Order	Family	Common name	Scientific name	Season	RA	
Wet	Dry	Total	
Anseriformes	Anatidae	Egyptian Goose	Alopochen aegyptiaca	87	365	452	12.7	
		African Pygmy-Goose	Nettapus auratus	0	43	43	1.2	
		Tufted Duck	Aythya fuligula	56	0	56	1.6	
		White-backed Duck	Thalassornis leuconotus	0	39	39	1.1	
		Knob-billed Duck	Sarkidiornis melanotos	0	32	32	0.9	
		Hottentot Teal	Spatula hottentota	0	12	12	0.33	
		Southern Pochard	Netta erythrophthalma	0	53	53	1.5	
		Green-winged Teal	Anas crecca	0	11	11	0.31	
Charadriiformes	Charadriidae	Three-banded Plover	Charadrius tricollaris	16	0	16	0.45	
		Kittlitz’s Plover	Charadrius pecuarius	13	0	13	0.4	
		Ringed Plover	Charadrius hiaticula	21	0	21	0.59	
		Little Ringed Plover	Charadrius dubius	10	0	10	0.28	
		Spur-winged Lapwing	Vanellus spinosus	46	116	162	4.54	
	Burhinidae	Spotted Thick-knee	Burhinus capensis	35	0	35	0.98	
	Scolopacidae	Common Sandpiper	Actitis hypoleucos	21	0	21	0.59	
		Marsh Sandpiper	Tringa stagnatilis	9	0	9	0.25	
		Green Sandpiper	Tringa ochropus	0	20	20	0.56	
		Common Snipe	Gallinago gallinago	62	0	62	1.74	
		African Snipe	Gallinago nigripennis	72	0	72	2.01	
		Jack Snipe	Lymnocryptes minimus	60	0	60	1.68	
		Great Sniped	Gallinago media	29	0	29	0.08	
		Eurasian Curlewd	Numenius arquata	41	0	41	1.15	
		Whimbrel	Numenius phaeopus	9	1	10	0.28	
		Stone Curlew	Burhinus oedicnemus	15	21	36	1.01	
		Ruff	Calidris pugnax	56	99	155	4.34	
		Temminck’s Stint	Calidris temmincki	0	36	36	1.01	
	Rostratulidae	Greater Painted-Snipe	Rostratula benghalensis	0	14	14	0.39	
	Recurvirostridae	Black-winged Stilt	Himantopus himantopus	6	0	6	0.17	
		Pied Avocet	Recurvirostra avosetta	10	0	10	0.28	
Pelecaniformes	Ardeidae	Cattle Egret	Bubulcus ibis	74	51	125	3.5	
		Little Egret	Egretta garzetta	37	23	60	1.68	
		Greater White Egret	Egretta alba	8	6	14	0.39	
		Gray Heron	Ardea cinerea	17	26	43	1.2	
		Goliath Heron	Ardea goliath	68	43	111	3.11	
		Purple Heron	Ardea purpurea	3	0	3	0.08	
		White-backed Night-Heron	Gorsachius leuconotus	0	56	56	1.57	
		Squacco Heron	Ardeola ralloides	0	8	8	0.22	
		Dwarf Bittern	Ixobrychus sturmii	0	22	22	0.62	
	Scopidae	Hamerkop	Scopus umbretta	2	4	6	0.17	
	Threskiorithidae	African Sacred Ibis	Threskiornis aethiopicus	59	0	59	1.65	
		Wattled Ibisa	Bostrychia carunculata	40	0	40	1.11	
	Pelecanidae	Pink-backed Pelican	Pelecanus rufescens	54	37	91	2.55	
		Great White Pelican	Pelecanus onocrotalus	35	48	83	2.32	
Suliformes	Anhingidae	African Darter	Anhinga rufa	4	23	27	0.76	
Passeriformes	Sturnidae	Greater Blue-eared Glossy-Starling	Lamprotornis chalybeus	37	18	55	1.54	
	Pycnonotidae	Common Bulbul	Pycnonotus barbatus	16	9	25	0.7	
	Turdidae	Groundscraper Thrush	Psophocicchla Litsitsirupa	14	0	14	0.39	
		Song Thrush	Turdus philomelos	8	0	8	0.22	
	Fringillidae	White-rumped Seedeater	Serinus leucopygius	9	0	9	0.25	
	Estrildidae	Common Waxbill	Estrilda astrild	11	0	11	0.31	
		Red-cheeked Cordon-Bleu	Uraeginthus bengalus	34	0	34	0.95	
		Blue-cheeked Cordon-Bleu	Uraeginthus angolensis	23	0	23	0.64	
	Muscicapidae	Mocking Cliff-chat	Thamnolaea cinnamomeiventris	18	0	18	0.5	
		White-winged Cliff-chatb	Thamnolaea semirufa	0	15	15	0.42	
		Spotted flycatcher	Muscicapa striata	16	0	16	0.46	
		Abyssinian Slaty Flycatcher	Melaenornis chocolatinus	0	21	21	0.59	
		African Dusky Flycatcher	Muscicapa adusta	0	9	90	0.25	
		Spotted Morning-Thrush	Cichladusa guttata	25	0	25	0.7	
		African Stonechat	Saxicola torquatus	0	3	3	0.08	
	Malaconotidae	Black-crowned Tchagra	Tchagra senegala	6	0	6	0.17	
	Laniidae	Greater Gray Shrike	Lanius excubitor	7	0	7	0.2	
		Common Fiscal	Lanius collaris	32	27	59	1.65	
		Gray-backed Fiscal	Lanius excubitoroides	14	0	14	0.39	
	Buphagidae	Yellow-billed Oxpecker	Buphagus africanus	8	0	8	0.22	
	Alaudidae	Singing Bushlark	Mirafra cantillans	17	0	17	0.48	
		Crested Lark	Galerida cristata	10	0	10	0.28	
		Flappet Lark	Mirafra rufocinnamomea	12	0	12	0.34	
		Thekla Lark	Galerida theklae	6	0	6	0.17	
	Motacillidae	Plain-backed Pipit	Anthus leucophrys	7	0	7	0.2	
		Mountain Wagtail	Motacilla clara	0	16	16	0.45	
	Sylviidae	Abyssinian Catbirda	Parophasma galinieri	5	0	5	0.14	
	Nectariniidae	Malachite Sunbird	Nectarinia famosa	7	0	7	0.2	
		Beautiful Sunbird	Nectarinia pulchella	13	0	13	0.36	
		Variable Sunbird	Cinnyris venustus	7	0	7	0.2	
		Scarlet-chested Sunbird	Chalcomitra senegalensis	0	7	7	0.2	
	Ploceidae	Black-headed Weaver	Ploceus cucullatus	19	22	41	1.15	
		Spectacled Weaver	Ploceus ocularis	0	27	27	0.76	
		Parasitic Weaver	Anomalospiza imberbis	0	19	19	0.53	
		Baglafecht Weaver	Ploceus baglafecht	0	16	16	0.45	
		Yellow-mantled Widowbird	Euplectes macrocercu	105	0	105	2.94	
		Red-collared Widowbird	Euplectes ardens	41	0	41	1.15	
		Black Bishop	Euplectes gierowii	37	0	37	1.04	
		Black-winged Red Bishop	Euplectes hordeaceus	20	0	20	0.56	
	Corvidae	Pied Crow	Carvus albus	10	0	10	0.28	
	Cisticolidae	Green-backed Camaroptera	Camaroptera brachyura	9	0	9	0.25	
		Red-faced Cisticola	Cisticola erythrops	0	12	12	0.34	
		Singing Cisticola	Cisticola cantans	0	9	9	0.25	
Gruiformes	Rallidae	Eurasian Coot	Fulica atra	61	0	61	1.71	
		Red-knobbed Coot	Fulica cristata	0	15	15	0.42	
		Rouget’s Raila,d	Rougetius rougetii	5	0	5	0.14	
Acipitroformes	Accipitiridae	Black Goshawk	Accipiter melanoleucus	11	0	11	0.31	
		Lizard Buzzard	Kaupifalco monogramicus	4	0	4	0.11	
		Common Buzzard	Buteo buteo	0	9	9	0.25	
		Black Kite	Milvus migrans	0	22	22	0.62	
		Yellow-billed Kite	Milvus aegyptius	0	6	6	0.17	
		Montagu’s Harrier	Circus pygargus	0	10	10	0.28	
		Greater Spotted Eagle	Clanga clanga	0	2	2	0.06	
Bucerotiformes	Bucerotidae	Hemprich’s Hornbill	Tockus hemprichii	6	0	6	0.17	
		African Gray Hornbill	Lophoceros nasutus	0	12	12	0.34	
	Phoeniculidae	Black-billed Wood-hoopoe	Phoeniculus somaliensis	0	25	25	0.7	
	Bucorvidae	Abyssinian Ground- Hornbillc	Bucorvus abyssinicus	4	0	4	0.11	
Coraciiformes	Alcedinidae	Pied Kingfisher	Ceryle rudis	16	13	29	0.81	
	Meropidae	White-throated Bee-eater	Merops albicollis	7	0	7	0.2	
		Blue-breasted Bee-eater	Merops variegatus	7	0	7	0.2	
	Coraciidae	European Roller	Coracias garrulus	3	0	3	0.08	
		Rufous-crowned Roller	Coracia naevius	8	0	8	0.22	
Ciconiiformes	Ciconiidae	Yellow-billed Stork	Mycteria ibis	4	0	4	0.11	
		Abdim’s Stork	Ciconia abdimii	5	0	5	0.14	
		Black Stork	Ciconia nigra	0	7	7	0.2	
		White Stork	Ciconia ciconia	6	0	6	0.17	
Coliiformes	Coliidae	Speckled Mousebird	Colius stariatus	12	7	19	0.53	
Columbiformes	Columbidae	Mourning Collared-Dove	Streptopelia decipiens	16	0	16	0.45	
		Ring-necked Dove	Streptopelia capicola	23	26	49	1.37	
		Dusky Turtle-Dove	Streptopelia lugens	9	0	9	0.25	
		Tambourine Dove	Turtur tympanistria	0	6	6	0.17	
		Speckled Pigeon	Columba guinea	12	15	27	0.76	
		Bruce’s Green-Pigeon	Treron waalia	6	0	6	0.17	
		Namaqua Dove	Oena capensis	0	13	13	0.36	
Piciformes	Picidae	Abyssinian Woodpeckera	Dendropicos abyssinicus	5	0	5	0.14	
	Lybiidae	Double-toothed Barbet	Lybius bidentatus	0	2	2	0.06	
Galliformes	Phasianidae	Scaly Francolin	Pternistis squamatus	3	0	3	0.08	
		Erckel’s Francolin	Pternistis erckelii	0	22	22	0.62	
Psittaciformes	Psittaculidae	Black-winged Lovebirdb	Agapornis taranta	10	0	10	0.28	
Where, aEndemic species, bNear-endemic, cVulnerable, dNear-threatened, RA relative abundance

Abbreviations

ANOVA Analysis of variance

GPS Global Positioning System

P Probability

PAST Paleontological Statistics

Acknowledgements

We would like to express our thanks to Aksum University and Ethiopian Biodiversity Institute, Mekelle Biodiversity Center for the facilities and financial support. Authors also sincerely thank to the local communities around Mai-Nigus reservoir for their delivery necessary information and hospitality during data collection such as giving orange, guava and roasted maize.

Authors’ contributions

A.A proposed the research idea. A.A, K.M and W.T collected the data and identified birds; A.A, K.M and B.F generated and analyzed the results; A.A, A.G and T.M interpreted the results and wrote the paper. All authors contribute, read and approved the final manuscript.

Funding

The study did not receive any specific financial support but performed by the willingness of authors using the perdiem from Aksum University and Mekelle Biodiversity Center.

Availability of data and materials

All the data generated and analyzed during this manuscript preparation are available on the hands of the corresponding author.

Data availability

No datasets were generated or analysed during the current study.

Declarations

Ethics approval and consent to participate

The study was approved by Research and Publication Directorate office of Aksum University and permission was obtained from the local government. Consent to participation is not applicable since no respondents were participated in this research work. All methods used in this study were performed in accordance with the relevant guidelines and regulations.

Consent for publication

Not applicable.

Competing interests

The authors declare no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
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References

1. Yalden D Largen M Endemic mammals of Ethiopia Mammal Rev 1992 22 115 150 10.1111/j.1365-2907.1992.tb00128.x
Yalden D, Largen M. Endemic mammals of Ethiopia. Mammal Rev. 1992;22:115–50.10.1111/j.1365-2907.1992.tb00128.x
2. Ash JS Atkins J Birds of Ethiopia and Eritrea: an atlas of distribution 2009 London, UK Christopher Helm
Ash JS, Atkins J. Birds of Ethiopia and Eritrea: an atlas of distribution. London, UK: Christopher Helm; 2009.
3. Lavrenchenko L Afework B Diversity and conservation of Ethiopian mammals: what have we learned in 30 years? Ethiop J Biol Sci 2017 16 1 20
Lavrenchenko L, Afework B. Diversity and conservation of Ethiopian mammals: what have we learned in 30 years? Ethiop J Biol Sci. 2017;16:1–20.
4. Weldemariam T A catalogue for endemic birds of Ethiopia J Zool 2016 3 4 109 133
Weldemariam T. A catalogue for endemic birds of Ethiopia. J Zool. 2016;3(4):109–33.
5. Lepage D. Checklist of the birds of Ethiopia: Avibase, the world bird database; 2020. http://www.bsceoc.org/avibase, Accessed 9 July 2023.
6. Lepage D. Checklist of the birds of Ethiopia: avibase, the world bird database. 2024. https://avibase.bsc-eoc.org/checklist.jsp?lang=EN®ion=et&list=clements&ref=l_afr_et. Accessed 15 June 2024.
7. EWNHS. Important bird areas of Ethiopia. A first inventory. Addis Ababa: Ethiopian Wildlife and Natural History Society (EWNHS); 1996.
8. Teklay G Zeyede T Tesfay T Bird diversity and community composition in Kafta Sheraro National Park, Tigray, Northern Ethiopia Int J Zool 2020 10.1155/2020/5016804
Teklay G, Zeyede T, Tesfay T. Bird diversity and community composition in Kafta Sheraro National Park, Tigray, Northern Ethiopia. Int J Zool. 2020. 10.1155/2020/5016804.10.1155/2020/5016804
9. Sekerciog C Gretchen H Daily C Ehrlich RP Ecosystem consequences of bird declines PANS 2004 101 52 18042 18047 10.1073/pnas.0408049101
Sekerciog C, Gretchen H, Daily C, Ehrlich RP. Ecosystem consequences of bird declines. PANS. 2004;101(52):18042–7.10.1073/pnas.0408049101
10. Rajashekara S Venkatesha MG The diversity and abundance of water birds in lakes of Bangalore city, Karnataka, India Biosystematica 2010 4 2 63 73
Rajashekara S, Venkatesha MG. The diversity and abundance of water birds in lakes of Bangalore city, Karnataka, India. Biosystematica. 2010;4(2):63–73.
11. Ramchandra AM Diversity and richness of bird species in newly formed habitats of Chandoli National Park in Western Ghats, Maharashtra State, India Biodivers J 2013 4 1 235 242
Ramchandra AM. Diversity and richness of bird species in newly formed habitats of Chandoli National Park in Western Ghats, Maharashtra State, India. Biodivers J. 2013;4(1):235–42.
12. Hailemariam A Meheretu Y Tsegazeabe H Community composition and abundance of residential birds in selected church forests, Tigray Region, Northern Ethiopia Sci Res Essays 2013 8 2 1038 1047
Hailemariam A, Meheretu Y, Tsegazeabe H. Community composition and abundance of residential birds in selected church forests, Tigray Region, Northern Ethiopia. Sci Res Essays. 2013;8(2):1038–47.
13. Whelan CJ Sekercioglu CH Wenny DG Why birds matter: from economic ornithology to ecosystem services J Ornithol 2015 156 1 1 13
Whelan CJ, Sekercioglu CH, Wenny DG. Why birds matter: from economic ornithology to ecosystem services. J Ornithol. 2015;156(1):1–13.
14. Zerihun G Girma M Tsyon A Diversity, relative abundance and distribution of avian fauna in and around Wondogenet forest, South-central Ethiopia Res J for 2017 11 1 1 12
Zerihun G, Girma M, Tsyon A. Diversity, relative abundance and distribution of avian fauna in and around Wondogenet forest, South-central Ethiopia. Res J for. 2017;11(1):1–12.
15. Kiros W Tsegazeab H Solomon K Mokonen T Kibrom F Meheretu Y Assessment of birds of the arid water bodies in Tigray, Northern Ethiopia Int J Biodivers Conserv 2014 6 4 333 341 10.5897/IJBC2014.0695
Kiros W, Tsegazeab H, Solomon K, Mokonen T, Kibrom F, Meheretu Y. Assessment of birds of the arid water bodies in Tigray, Northern Ethiopia. Int J Biodivers Conserv. 2014;6(4):333–41.10.5897/IJBC2014.0695
16. Mason NW Mouillot D Lee WG Wilson JB Functional richness, functional evenness and functional divergence: the primary components of functional diversity Oikos 2005 111 112 118 10.1111/j.0030-1299.2005.13886.x
Mason NW, Mouillot D, Lee WG, Wilson JB. Functional richness, functional evenness and functional divergence: the primary components of functional diversity. Oikos. 2005;111:112–8.10.1111/j.0030-1299.2005.13886.x
17. Aerts R Lerouge F November E Land rehabilitation and the conservation of birds in a degraded afromontane landscape in northern Ethiopia Biodivers Conserv 2008 17 53 69 10.1007/s10531-007-9230-2
Aerts R, Lerouge F, November E, et al. Land rehabilitation and the conservation of birds in a degraded afromontane landscape in northern Ethiopia. Biodivers Conserv. 2008;17:53–69.10.1007/s10531-007-9230-2
18. Mengesha G Bekele A Diversity and relative abundance of birds of Alatish National Park, North Gondar, Ethiopia Int J Ecol Environ Sci 2008 34 215 222
Mengesha G, Bekele A. Diversity and relative abundance of birds of Alatish National Park, North Gondar, Ethiopia. Int J Ecol Environ Sci. 2008;34:215–22.
19. Mengesha G Mamo Y Bekele A A comparison of terrestrial bird community structure in the undisturbed and disturbed areas of the Abijata Shalla lakes national park, Ethiopia Int J Biodivers Conserv 2011 3 389 404
Mengesha G, Mamo Y, Bekele A. A comparison of terrestrial bird community structure in the undisturbed and disturbed areas of the Abijata Shalla lakes national park, Ethiopia. Int J Biodivers Conserv. 2011;3:389–404.
20. Shimelis A Afework B Species composition, relative abundance and distribution of bird fauna of riverine and wetland habitats of Infranz and Yiganda at Southern Tip of Lake Tana, Ethiopia Trop Ecol 2008 49 2 199 209
Shimelis A, Afework B. Species composition, relative abundance and distribution of bird fauna of riverine and wetland habitats of Infranz and Yiganda at Southern Tip of Lake Tana, Ethiopia. Trop Ecol. 2008;49(2):199–209.
21. Donald PE Sanderson FJ Burfield IJ Further evidence of continent-wide impacts of agricultural intensification on European farmland birds, 1990–2000 Agric Ecosyst Environ 2006 116 189 196 10.1016/j.agee.2006.02.007
Donald PE, Sanderson FJ, Burfield IJ, et al. Further evidence of continent-wide impacts of agricultural intensification on European farmland birds, 1990–2000. Agric Ecosyst Environ. 2006;116:189–96.10.1016/j.agee.2006.02.007
22. Amare G Zelalem T Diversity and threats of avifauna in Cheleleka Wetland, Central Rift Valley of Ethiopia Res Ecol 2020 2 3 53 60
Amare G, Zelalem T. Diversity and threats of avifauna in Cheleleka Wetland, Central Rift Valley of Ethiopia. Res Ecol. 2020;2(3):53–60.
23. Selamawit N Seid T Peter LM Goethals L Pieter B Effect of human-Induced Environmental changes on bird diversity and abundance in Natural wetlands of Southwest Ethiopia Waterbirds 2017 40 2 129 143 10.1675/063.040.0205
Selamawit N, Seid T, Peter LM, Goethals L, Pieter B. Effect of human-Induced Environmental changes on bird diversity and abundance in Natural wetlands of Southwest Ethiopia. Waterbirds. 2017;40(2):129–43.10.1675/063.040.0205
24. Hadis T Afework B Simeneh A Significance of Gefersa Artificial Reservoir and its surrounding habitat for the conservation of avifauna, Northwestern Addis Ababa, Ethiopia Species 2020 21 67 53 61
Hadis T, Afework B, Simeneh A. Significance of Gefersa Artificial Reservoir and its surrounding habitat for the conservation of avifauna, Northwestern Addis Ababa, Ethiopia. Species. 2020;21(67):53–61.
25. Weldemariam T Alembrhan A Diversity and abundance of birds in dumpsites of Afar region, Ethiopia: implication for conservation BMC Zool 2023 8 16 10.1186/s40850-023-00177-6 37653462
Weldemariam T, Alembrhan A. Diversity and abundance of birds in dumpsites of Afar region, Ethiopia: implication for conservation. BMC Zool. 2023;8:16.37653462 10.1186/s40850-023-00177-6
26. Abeba A Nega T Dessalegn E Seasonal diversity of urban birds: the case of Bahir Dar city, Ethiopia Ethiop J Biol Sci 2020 19 2 181 207
Abeba A, Nega T, Dessalegn E. Seasonal diversity of urban birds: the case of Bahir Dar city, Ethiopia. Ethiop J Biol Sci. 2020;19(2):181–207.
27. Tsehaye A, Tadesse D, Declerck S, Nyssen J, Van der Gucht K, Risch S, Rousseaux S, De Wit J, Afework M, Nigussie H, Abreha G, Poesen J, Deckers J, Vyverman W, De Meester L. Ecological atlas of reservoirs in Tigray, Northern Ethiopia. Tigray Livelihood Papers No. 4, VLIR - Mekelle University IUC Programme, Ethiopia; 2007.
28. Alemayehu S Dereje Y Diversity, distribution and relative abundance of avifauna at Ansas Dam and surrounding farmland site Debre Birhan Town, Ethiopia Avian Biol Res 2021 14 1 8 17 10.1177/1758155920963200
Alemayehu S, Dereje Y. Diversity, distribution and relative abundance of avifauna at Ansas Dam and surrounding farmland site Debre Birhan Town, Ethiopia. Avian Biol Res. 2021;14(1):8–17.10.1177/1758155920963200
29. Dessalegn T Melaku W Diversity, abundance and threats of avian species in Koga dam and its surroundings, North-western Ethiopia SINET: Ethiop J Sci 2017 40 2 60 73
Dessalegn T, Melaku W. Diversity, abundance and threats of avian species in Koga dam and its surroundings, North-western Ethiopia. SINET: Ethiop J Sci. 2017;40(2):60–73.
30. Amare G Girma M Species diversity and relative abundance of Avifauna in Lake Hawasa and its adjoining areas, Ethiopia J Biodivers Endanger Species 2019 7 3 234
Amare G, Girma M. Species diversity and relative abundance of Avifauna in Lake Hawasa and its adjoining areas, Ethiopia. J Biodivers Endanger Species. 2019;7(3):234.
31. Climate-Data.org. Axum - Climate graph, Temperature graph, Climate table. https://en.climate-data.org. Retrieved 10 June 2024.
32. Buckland ST Anderson DR Burnham KP Laake JL Borchers DL Introduction to Distance Sampling: estimating abundance of Biological populations 2001 Oxford, UK Oxford University Press
Buckland ST, Anderson DR, Burnham KP, Laake JL, Borchers DL. Introduction to Distance Sampling: estimating abundance of Biological populations. Oxford, UK: Oxford University Press; 2001.
33. Ayalew D Sintayehu T Ermias K Girma M Diversity and relative abundance of birds in Loka Abaya National Park, Sidama Zone, Southern Ethiopia Int J Biodivers Conserv 2019 11 8 230 240 10.5897/IJBC2019.1306
Ayalew D, Sintayehu T, Ermias K, Girma M. Diversity and relative abundance of birds in Loka Abaya National Park, Sidama Zone, Southern Ethiopia. Int J Biodivers Conserv. 2019;11(8):230–40.10.5897/IJBC2019.1306
34. Vergara MP Jim´enez EJ Schlatter PR Effective point-count duration for estimating bird species’ richness in Chilean forests Zool Stud 2010 49 381 91
Vergara MP, Jim´enez EJ, Schlatter PR. Effective point-count duration for estimating bird species’ richness in Chilean forests. Zool Stud. 2010;49:381–91.
35. Bibby C Jones M Marsden S Bird surveys. Expedition field techniques 1998 London, UK The Expedition Advisory Center Royal Geographic Society
Bibby C, Jones M, Marsden S. Bird surveys. Expedition field techniques. London, UK: The Expedition Advisory Center Royal Geographic Society; 1998.
36. Perlo BV Birds of Eastern Africa 2009 Hong Kong, China Collis Field Guide Harper Collins
Perlo BV. Birds of Eastern Africa. Hong Kong, China: Collis Field Guide Harper Collins; 2009.
37. Redman R Stevenson T Fanshawe J Birds of the Horn of Africa: Ethiopia, Eritrea, Djibouti, Somalia, and Socotra 2009 NJ, USA Princeton University Press. Princeton
Redman R, Stevenson T, Fanshawe J. Birds of the Horn of Africa: Ethiopia, Eritrea, Djibouti, Somalia, and Socotra. NJ, USA: Princeton University Press. Princeton; 2009.
38. Hammer O Harper D Ryan P PAST: Paleontological Statistics Software Package for Education and Data Analysis Palaeontol Electron 2001 4 1 1 9
Hammer O, Harper D, Ryan P. PAST: Paleontological Statistics Software Package for Education and Data Analysis. Palaeontol Electron. 2001;4(1):1–9.
39. Kathleen A Nolan K Callahan JE The Shannon-Weiner species diversity index Beachcomber Biology 2005 27 334 338
Kathleen A, Nolan K, Callahan JE. The Shannon-Weiner species diversity index. Beachcomber Biology. 2005;27:334–8.
40. Jeffery C Diane M Debinsi O Jakubausk S Aelly K Beyond species richness, community similarity as a measure of cross taxon congruence for coarse filter conservation Conserv Biol 2004 18 167 173 10.1111/j.1523-1739.2004.00337.x
Jeffery C, Diane M, Debinsi O, Jakubausk S, Aelly K. Beyond species richness, community similarity as a measure of cross taxon congruence for coarse filter conservation. Conserv Biol. 2004;18:167–73.10.1111/j.1523-1739.2004.00337.x
41. McCaskie G Shorebirds and waterbirds use of Salton Sea Calif Fish Game 1970 66 2 87 95
McCaskie G. Shorebirds and waterbirds use of Salton Sea. Calif Fish Game. 1970;66(2):87–95.
42. Bull G Birds of New York State 1974 London, UK Cornell University Press
Bull G. Birds of New York State. London, UK: Cornell University Press; 1974.
43. Ali AMS Kumar SR Arun PR Waterbirds assemblage in rural ponds of Samakhiali region, Kutch district, Gujarat, India Bird Populations 2013 12 12 18
Ali AMS, Kumar SR, Arun PR. Waterbirds assemblage in rural ponds of Samakhiali region, Kutch district, Gujarat, India. Bird Populations. 2013;12:12–8.
44. Batary P Fronczek S Normann C Scherber C Tscharntke T How do edge effect and tree species diversity change bird diversity and avian nest survival in Germany’s largest deciduous forest? Ecol Mana 2014 319 44 50 10.1016/j.foreco.2014.02.004
Batary P, Fronczek S, Normann C, Scherber C, Tscharntke T. How do edge effect and tree species diversity change bird diversity and avian nest survival in Germany’s largest deciduous forest? Ecol Mana. 2014;319:44–50.10.1016/j.foreco.2014.02.004
45. Ziyad J Zerihun G Girma M Bird Diversity in Nensebo Moist Afromontane Forest Fragment, South Eastern Ethiopia Open Ornithol J 2020 13 1 9 10.2174/1874453202013010001
Ziyad J, Zerihun G, Girma M. Bird Diversity in Nensebo Moist Afromontane Forest Fragment, South Eastern Ethiopia. Open Ornithol J. 2020;13:1–9.10.2174/1874453202013010001
46. Yenew G Dessalegn E Community composition, relative abundance and habitat association of avian species in Apini and Dikuma forest patches, Awi Administrative Zone, Ethiopia Ethiop J Sci Technol 2017 10 1 33 50 10.4314/ejst.v10i1.3
Yenew G, Dessalegn E. Community composition, relative abundance and habitat association of avian species in Apini and Dikuma forest patches, Awi Administrative Zone, Ethiopia. Ethiop J Sci Technol. 2017;10(1):33–50.10.4314/ejst.v10i1.3
47. Tamenut D Shimelis A Nega T Diversity, abundance and habitat association of avifauna in Menagesha Amba Mariam and Gara Medhanialem forest in Oromia Region, Ethiopia Int J Avian Wildl Biol 2021 6 1 1 10
Tamenut D, Shimelis A, Nega T. Diversity, abundance and habitat association of avifauna in Menagesha Amba Mariam and Gara Medhanialem forest in Oromia Region, Ethiopia. Int J Avian Wildl Biol. 2021;6(1):1–10.
48. Gaston KJ Blackburn TM Greenwood JB Greroryx RD Rachel MQ Lawton JH Abundance-occupancy relationships J Appl Ecol 2000 37 39 59 10.1046/j.1365-2664.2000.00485.x
Gaston KJ, Blackburn TM, Greenwood JB, Greroryx RD, Rachel MQ, Lawton JH. Abundance-occupancy relationships. J Appl Ecol. 2000;37:39–59.10.1046/j.1365-2664.2000.00485.x
49. Froneman AJ Mangnall RM Crowe TM Water bird assemblages and associated habitat characteristics of farm ponds in the Western Cape, South Africa Biodivers Conserv 2001 10 251 270 10.1023/A:1008904421948
Froneman AJ, Mangnall RM, Crowe TM. Water bird assemblages and associated habitat characteristics of farm ponds in the Western Cape, South Africa. Biodivers Conserv. 2001;10:251–70.10.1023/A:1008904421948
50. Seyoum K Bezawork A Kebeta L A preliminary study on bird diversity and abundance from Wabe fragmented forests around Gubre subcity and Wolkite town, Southwestern Ethiopia Int J Avian Wildl Biol 2018 3 5 333 340
Seyoum K, Bezawork A, Kebeta L. A preliminary study on bird diversity and abundance from Wabe fragmented forests around Gubre subcity and Wolkite town, Southwestern Ethiopia. Int J Avian Wildl Biol. 2018;3(5):333–40.
51. Ryan PG Owino OA Habitat association of papyrus specialist birds at three papyrus swamps in western Kenya Afr J Ecol 2006 44 438 443 10.1111/j.1365-2028.2006.00652.x
Ryan PG, Owino OA. Habitat association of papyrus specialist birds at three papyrus swamps in western Kenya. Afr J Ecol. 2006;44:438–43.10.1111/j.1365-2028.2006.00652.x
