Journal of Threatened Taxa | www.threatenedtaxa.org | 26 August 2022 | 14(8): 21561–21578

 

ISSN 0974-7907 (Online) | ISSN 0974-7893 (Print) 

https://doi.org/10.11609/jott.7067.14.8.21561-21578

#7067 | Received 11 January 2021 | Final received 09 August 2022 | Finally accepted 12 August 2022

 

 

Avifaunal diversity in unprotected wetlands of Ayodhya District, Uttar Pradesh, India

 

Yashmita-Ulman 1  & Manoj Singh 2

 

1 Department of Silviculture and Agroforestry, Acharya Narendra Deva University of Agriculture and Technology, Ayodhya, Uttar Pradesh 224229, India.

2 Department of Zoology, Kalinga University, Naya Raipur, Chhattisgarh 492101, India.

1 yashmita2018@gmail.com, 2 msingh.zooku@gmail.com (corresponding author)

 

 

 

Editor: Hem S. Baral, Charles Sturt University, Aldbury, Australia.     Date of publication: 26 August 2022 (online & print)

 

Citation: Yashmita-Ulman & M. Singh (2022). Avifaunal diversity in unprotected wetlands of Ayodhya district, Uttar Pradesh, India. Journal of Threatened Taxa 14(8): 21561–21578. https://doi.org/10.11609/jott.7067.14.8.21561-21578

 

Copyright: © Yashmita-Ulman & Singh 2022. Creative Commons Attribution 4.0 International License.  JoTT allows unrestricted use, reproduction, and distribution of this article in any medium by providing adequate credit to the author(s) and the source of publication.

 

Funding: Self-funded.

 

Competing interests: The authors declare no competing interests.

 

Author details: Dr. Yashmita-Ulman, is an Assistant Professor at Department of Silviculture & Agroforestry, ANDUAT, Ayodhya. She has been involved in research on wildlife. Her current interests include plant-animal interactions in agroforestry systems and forests. Dr. Manoj Singh is an Assistant Professor at Department of Zoology, Kalinga University, Chhattisgarh. He is working on bird acoustics and wildlife conservation using GIS.

 

Author contributions: Y-U was involved in data collection. Both the authors were involved in data compilation, analysis, manuscript writing, editing and finalizing the manuscript.

 

Acknowledgements: The authors are thankful to the Dean, College of Horticulture and Forestry, ANDUAT, for permitting to carry out this field research. Our special thanks to Mr. Abhishek Kumar Pandey for translating the abstract in Hindi.

 

 

 

Abstract: Nine unprotected wetlands of Ayodhya district, Uttar Pradesh, India were studied to assess the bird species composition and richness from March 2019 to February 2020 using point count method. A total of 105 species of birds belonging to 79 genera, distributed among 35 families and 12 orders were recorded. Passeriformes had the highest diversity with 25 species and 12 families. Anatidae was the most dominant family with 15 species, constituting 14.29% of the wetland bird community in the study area. These wetlands provided habitat for 62 residential species, 42 winter migrants and one vagrant. The carnivore guild was the most dominant with 46 species. The wetland sites under study were continuously used by humans mainly for land encroachment, fishing activities and livestock grazing apart from other minor uses. Out of the nine selected wetlands, three wetlands (˂2 ha) had very few bird species (≤3), therefore were excluded from further calculations. But the rest of the six selected wetlands (˃5 ha) provided habitat for 12 bird species of conservation importance (one Endangered species, five Vulnerable species, and six Near Threatened species) according to the IUCN Red list. These wetlands also supported 39 species of birds having a declining population trend globally. These findings highlight the role of medium and large-sized unprotected wetlands in providing critical habitat to the birds throughout the year in Ayodhya district. Future research must concentrate on understanding the key factors influencing the presence and absence of birds in such unprotected wetlands so that these wetlands can be managed effectively to secure the potential habitat of birds.

 

Keywords: Birds, conservation importance, feeding guild, relative diversity index, species richness.

 

 

INTRODUCTION

 

Wetlands are transitional zones between terrestrial and aquatic ecosystems, which can be permanently or seasonally flooded but retain saturated soils throughout the unflooded period (TWI 2020). Wetlands occupy about 6% of the earth’s surface, comprising bogs (30%), fens (26%), swamps (20%), and flood plains (15%) (Shine & Klemm 1999). Wetlands are highly diverse and biologically rich, providing habitats to many groups of species like waterbirds, fish, amphibians, reptiles, invertebrates, mammals, and plants. Wetlands play an important role in maintaining the hydrological cycle. The other services provided by wetlands include flood protection, water purification and recreational opportunities (Woodward & Wui 2001). Birds are an inseparable entity in wetland ecosystems as they play an important role in nutrient recycling and occupy different trophic levels in the food web (Custer & Osborn 1977; Rajashekara & Venkatesha 2010). Birds also act as useful bio-indicators reflecting the ecological health of the wetland ecosystems (Custer & Osborn 1977).  Wetlands are important for resident as well as migratory birds as they provide them with foraging, breeding, & nesting habitats and sometimes also serve as stopover sites (Kumar et al. 2016). India has around 4.7% of the total geographical area of the country under wetlands (Bassi et al. 2014). Nearly 310 bird species are reported to be wetland dependent in India (Kumar et al. 2005). Uttar Pradesh has 12,42,530 ha of area under wetlands, i.e., 5.16% of the total geographical area, whereas Ayodhya district has 23,050 ha, i.e., 1.86% of land under wetlands (NWA 2010). Many wetlands in this region are under threat due to anthropogenic pressure like conversion of wetlands into agricultural lands or for commercial fishing purposes, fertilizers run-offs from surrounding agricultural lands, hunting, unsustainable harvest of wetland resources, invasion of alien species, eutrophication, extraction of edible nuts of Trapa natans, pumping out water for agricultural purposes (Yashmita-Ulman pers. Comm. February 2020) thus, threatening the very existence of the resident and migratory wetland birds. Unprotected wetlands defined as those wetlands which have no official protection or conservation status and are also open for public use (Blanckenberg et al. 2020), are usually ignored, but such wetlands too provide the required habitat to the birds. So, to understand the anthropogenic impacts on wetland birds and their habitat in the future, it is necessary to have a baseline information on the species occurrences and habitat choices. Such information will also help in long term monitoring of the habitat and preparing conservation and management strategies for the species as well as their habitat. This exercise will also highlight the ecological health of the wetlands. The bird species checklist thus generated will provide a base for further research.    

The state of Uttar Pradesh has been reported to host 528 bird species (eBird 2021). It has eight wetlands listed under Ramsar Sites, which is the highest in India as compared to any other state. In addition to this, the state has many unprotected wetlands. But most of the studies on biodiversity in wetlands of Uttar Pradesh are concentrated on Ramsar and protected wetland sites. Studies have been conducted on plant diversity (Reddy et al. 2009), land-use changes (Behera et al. 2012) in Samaspur Bird Sanctuary, Rae Bareli, on plant diversity (Jha 2013) in Sandi Bird Sanctuary, Hardoi, and on butterfly diversity (Sharma 2007), medicinal plant diversity (Rani et al. 2009) & water quality monitoring (Gopal et al. 2015) in Sur Sarovar wetlands. There has been a study on bird diversity in agricultural landscapes of Ayodhya district (Yashmita-Ulman & Singh 2021), but there are no studies on wetlands of this district. As most of the wetlands present in Ayodhya district are either isolated, disturbed, unprotected or not designated as Ramsar sites, the inventories of these wetlands have not been done so far. So, this study is the first attempt to prepare a checklist of birds present in some selected unprotected wetlands of Ayodhya district.

 

 

MATERIALS AND METHODS

 

Study Area

Depending upon factors like easy accessibility and financial feasibility, three tehsils namely, Milkipur, Sohawal and Sadar of Ayodhya district (Figure 1) were chosen for the survey. Regular monitoring of the selected wetlands in these tehsils was possible as these tehsils fell in the daily commute route of the authors, i.e., from Rikabganj (Sadar tehsil) to Acharya Narendra Deva University of Agriculture and Technology (Milkipur tehsil) via NH 330A. The areas under these three tehsils were thoroughly searched for the presence of wetlands through google maps. Once the wetlands were identified, the areas were visited for ground truthing and preliminary bird survey. Depending on the presence of motorable roads, preliminary bird surveys and information from local people, a total of nine wetlands, three from each tehsil were selected for monthly bird surveys. Out of these nine wetlands, three wetlands (˂2 ha) supported very few bird species (≤3) and that too on an irregular basis (Table 1). So, data from these wetlands was not included in further analysis to avoid discrepancies in results. Therefore, this study reports the analyzed results only from six unprotected wetlands, three from Milkipur tehsil (Udaila Talab (Figure 1 & Image 1a), Sirsa Jheel (Figure 1 & Image 1b), & Barunshahganj Talab (Figure 1 & Image 1c); two from Sohawal tehsil (Jagdishpur Talab (Figure 1 & Image 1d) & Samda Jheel (Figure 1 & Image 1e); and one from Sadar tehsil (Kosiparikrama Nallah (Figure 1,2f) of Ayodhya district, Uttar Pradesh.

Ayodhya district is situated between 26.7730 °N and 82.1458 °E, and has an elevation of 93 m (KVK 2021). This district has an area of around 2,764 km2 (KVK 2021). Ayodhya city is situated on the banks of the river Ghagra locally known as ‘Saryu’. The climate is humid (Kumar 2018) and experiences summer season from March to June, rainy season from July to October and winter season from November to February (Sundar & Kittur 2012). The annual rainfall of the district is around 1,067 mm. The average temperature is 32 0C during summer season and 16 0C during winter season (KVK 2021). Oryza sativa – Triticum aestivum is the main cropping system. Saccharum officinarum and Brassica juncea are also grown in the area along with horticultural crops (Mangifera indica, Psidium guajava, Phyllanthus emblica, and Musa sp.) (KVK 2021). The detailed description of the selected unprotected wetlands is given in Table 1.

 

Methods

Bird surveys were conducted monthly using point-count method (Bibby et al. 2000) in the selected study sites from March 2019 to February 2020. Two point counts were fixed on the perimeter of each wetland making a total of 18 point counts in the whole district. In the same wetland the distance between the two point counts was at least 250 m. Each point count was surveyed 24 times during the entire study duration. After arriving at each point count, the observations of the initial 5 mins were not recorded giving time for the birds to settle down. After the initial 5 mins, bird species were recorded for the next 15 mins at the same point. During winters, fog conditions affected visibility early in the morning, so the observations were made whenever visibility was good (usually between 1000 to 1230 h) and for the rest of the seasons survey was conducted between 0600 to 0830 h. Birds were recorded directly with the help of field binoculars (Nikon 7x35). On each sighting, the details such as, species name, number of individuals and habitat were recorded. Birds flying across were not counted. The opportunistic counts were also recorded during other times of the day by scanning the periphery or banks of the wetlands. Grimmett et al. (2011) was used for bird identification and for knowing the residential status of birds (residents, winter visitor, summer visitor). Praveen et al. (2020) was followed for the taxonomic position and names. The classification of birds into major feeding guilds was done using Ali & Ripley (1987) and field observations. The IWPA (1972) and CITES (2012) were followed for assigning the conservation status of species. The Red List of IUCN (2021) was followed to compile the conservation status and the global population trend (decreasing, increasing, stable, unknown) of the recorded species.

Species richness was calculated as total number of bird species recorded in the study area.

The following community parameters were calculated using the below given formulae:

 [i] Relative diversity of bird families (RDi) (Torre-Cuadros et al. 2007)

            Number of bird species in a family

RDi = ––––––––––––––––––––––––––––––––– x 100

                    Total number of species

[ii] Shannon Weiner index (Shannon & Weiner 1963)

        

 

where, pi is often the proportion of individuals belonging to the ‘i’th species in the dataset and ‘s’ is the species richness. The values usually lies between 1 and 4 where 1 shows less diversity and 4 shows high diversity.

[iii] Margalef Richness Index (Margalef 1958)

                                                         S–1

Margalef Richness Index (D) = –––––––

                                                       Log (n)

where, ‘S’ is the total number of species and ‘n’ is the total number of individuals in the sample.

[iv] Simpson’s index (Simpson 1949)

This was calculated according to Simpson (1949) to measure the concentration of dominance (CD) of bird species.

 

 

where pi is the proportion of the Importance Value Index (IVI) of the ‘i’th species and IVI of all the species (ni/N). The values of Simpson’s index is limited to 1 where 1 shows dominance by a single species.

[v] Pielou’s evenness index (Pielou 1966) = H’/log10N(S)

where H’ is the Shanon Weiner Index of diversity and S is the total number of species.

This index ranges from 0 (no evenness) to 1 (complete evenness).

[vi] Sorenson’s similarity coefficient (Sorenson 1948)

                                              2C

Sorenson similarity coefficient = ––––

                                             A+B

where C is the number of species common to both sites, A is the total number of species in site A, and B is the total number of species in site B. Sorenson’s coefficient gives a value between 0 and 1, the closer the value is to 1, the more the communities have in common.

 

 

RESULTS

 

Out of nine wetlands, three wetlands (˂2 ha) had very few bird species (≤3) and that too on an irregular basis and were not considered in calculations to avoid discrepancies in results (Table 1). A total of 105 species of birds belonging to 79 genera, distributed among 35 families and 12 orders were recorded from the six unprotected wetlands of Ayodhya district, Uttar Pradesh during the study period (Table 2). Out of 105 species found, 73 species were wetland-associated and 32 species were terrestrial. Among the recorded bird species, 45 species (42.85%) were found commonly at all the six unprotected wetlands and 60 species (57.14%) were found at specific unprotected wetlands sites (Table 2). Passeriformes had the highest diversity with 25 species and 12 families, followed by Charadriiformes with 22 species from eight families (Figure 3). Anatidae was the most dominant family with 15 species and the highest RDi value (14.29) (Table 3). This was followed by Accipitridae with 10 species (Figure 2). Acrocephalidae, Alaudidae, Anhingidae, Columbidae, Dicruridae, Falconidae, Glareolidae, Gruidae, Laridae, Leiothrichidae, Pandionidae, Passeridae, Phylloscopidae, Recurvirostridae, Rostratulidae were represented by just a single genus and were the least represented (Figure 2).

Of all the bird species recorded, 62 species (59.05%) were resident, 42 species (40.00%) were winter visitors and one species (0.95%) was vagrant. As far as the foraging habit of the bird community in the selected wetland sites were concerned, five major feeding guilds were identified (Figure 3). The carnivore guild was the most dominant with 46 species (43.81%), followed by omnivore 42 species (40.00%), insectivore 15 species (14.29%) and frugivore and granivore with one species each (0.95%) (Figure 3). The maximum number of bird species were recorded in the months of January and February (89 each) and the least was recorded in the month of August (Figure 4). The unprotected wetland sites of Ayodhya district supported one Endangered species—Aquila nipalensis, five Vulnerable species—Antigone antigone, Aquila rapax, Aythya ferina, Clanga hastata, & Sterna aurantia, and six Near Threatened species—Anhinga melanogaster, Ciconia episcopus, Mycteria leucocephala, Vanellus duvaucelii, Esacus recurvirostris, & Threskiornis melanocephalus (Table 2). Moreover, these wetlands supported 39 species (37.14%) of birds having a declining population trend globally (Table 2).

The Shannon-Weiner index and Margalef richness index across the six unprotected wetland sites revealed that Udaila Talab was the most diverse and species rich wetland (3.86, 26.94) with 92 species (Table 4). This was followed by Samda Jheel (3.82, 25.41), Sirsa Jheel (3.80, 24.52), Jagdishpur Jheel (3.63, 23.66), Kosiparikrama Nallah (3.62, 23.82).  Barunshahganj Talab (3.55, 22.59) was found to be the least diverse of all (Table 4). All the wetlands showed diverse species and no single species showed dominancy (Table 4). The similarity in species composition of birds was measured using Sorenson’s similarity index (Table 5), the results of which highlighted that Udaila Talab and Samda Jheel showed the highest similarity (0.91) in bird communities, followed by Udaila Talab and Sirsa Jheel (0.89) and Samda Jheel and Sirsa Jheel (0.88) (Table 5). The least bird species similarity was shown between Jagdishpur Jheel and Kosiparikrama Nallah (0.76) (Table 5).

 

DISCUSSION

 

In this survey, the Passeriformes was the dominant order which conforms to the studies of Kumar & Sharma (2018). Family Anatidae was the most dominant of all families of bird species found in the selected unprotected wetlands of Ayodhya district. Similar results were found by Kumar & Gupta (2009), Tak et al. (2010), Chopra & Sharma (2012), and Kumar et al. (2016). Nearly 60% of the bird species found were resident. This result conforms to the studies of Mazumdar (2019) who also recorded the majority of birds to be resident in nature. In the present study, it was found that the birds belonged to five feeding guilds, the dominant guild being carnivores, followed by omnivores. This finding implies that the wetlands catered to the needs of the birds providing them with diverse food items like fish, crustaceans, invertebrates, water plants and plankton (Basavarajappa 2006).

The highest species richness was recorded in the months of January and February (89 species each) which conforms to the observations of Mazumdar (2019) in Okhla Bird Sanctuary, Uttar Pradesh. It was found that the bird species starts to increase from October and reaches the maximum in the months of January and February (Figure 4). This is due to the migrating waterfowls which arrive in the wetlands during this season as Uttar Pradesh is a part of the Central Asian Flyway serving as a wintering ground for these species. This is also one of the reasons for recording a high number of winter visitors (42 species) in this study. The wetlands along with the agricultural landscapes in Ayodhya district prove to be a good habitat for these migratory birds and therefore support a high diversity, especially in winters (Yashmita-Ulman & Singh 2021). These migratory species gradually start flying back to their breeding grounds from March so, the species richness declines slowly from March and reaches the lowest in the monsoon months (Figure 4). 

The wetland avian diversity and composition are influenced by factors like wetland size, location, vegetation (Sundar & Kittur 2013), type and level of anthropogenic activities, presence of additional and diverse foraging ground (Yashmita-Ulman & Singh 2021), water depth and quality (Saygili et al. 2011). Moreover, water birds usually prefer shallow water bodies with variations in depth (Helmers 1992; Colwell & Taft 2000). The Udaila Talab was surrounded by agricultural fields and had diverse vegetation like floating hydrophytes (Azolla pinnata, Eichhornia cracipes, Jussiaea repens, Ipomoea aquatica) and submerged hydrophytes (Najas graminea, Potamogeton nodosus). Trees like Eucalyptus tereticornis, Phyllanthus emblica, and Mangifera indica were found on the edge of the water body. It was a large sized water body with shallow water. Moreover, the undulating topography of the wetland gave rise to natural mounds and small isolated islands which served as resting places for the various bird species. As, Udaila Talab might have met all the requirements of bird species like alternative and diverse food supply, water depth variations, diverse microhabitats, it has registered as the wetland with the highest species richness and diversity. As far as both Sirsa and Samda Jheel were concerned, they both were surrounded with agricultural fields and trees, haboured rooted and emergent plants and had large areas under shallow water and marshy lands. Artificial mounds had been built in Samda Jheel by the Forest department to provide resting places to the water birds. All these factors might have attracted birds towards these jheels. So, both the wetlands supported a high avian diversity after Udaila Talab.

Deep waters are less preferred by waterbirds as they reduce the availability and accessibility of invertebrates (Murkin & Kadlec 1986). The Jagdishpur Jheel and Kosiparikrama Nallah therefore, had less to offer to the birds as they had higher water depths. Most of the birds found in these sites were restricted to the edge of the water bodies where the water was shallow. Only some ducks were found foraging in deep water. Moreover, the sewage water of the city of Ayodhya is drained into the Kosiparikrama Nallah and later this nallah merges with the Saryu river. So, mainly the birds like Himantopus himantopus which prefer feeding in polluted waters were found abundantly in this wetland. Both these wetlands were also smaller in size as compared to the other six wetlands in the study area. All these factors might be the reason for lower bird diversity in these wetlands as compared to Udaila Talab. On the other hand, though the Barunshahganj Talab has shallow water depth, it is a highly disturbed site as it lies next to the state highway NH 330A and has increasing land encroachment problems and is, therefore, shrinking in size and thus might have resulted in the lowest avian diversity as compared to the other wetlands in the study area.

It can be clearly understood from this study that all the wetlands in the study area have a great potential for conservation of avian communities. Though all the six wetlands under study were unprotected and had tremendous anthropogenic pressure, they were still capable of fulfilling the feeding, nesting and breeding requirements of the birds, and thus proved to be an optimum habitat. All the six wetlands in the study area had highly heterogeneous and mosaic of microhabitats as they were surrounded either by agricultural fields, orchards or plantations. The various tree species on the banks of wetlands provided the sites for perching, roosting and nesting of kingfishers, egrets, raptors, herons, cormorants and storks. The wading birds like storks, herons, ibises, snipe, redshank were found in shallow water and marshes. The wagtails, swamphens, waterhens and kingfishers were found in the adjoining agricultural fields as also reported by Urfi (2003). The plovers and sandpipers were found in the marshes. The waders like jacanas, egrets, herons, storks, ibises were found mostly feeding on Nymphea sp. The swimming and diving birds like coots, swamphens, ducks, cormorants, teal feasted on submerged vegetation (Vallisneria sp., Ceratophylum sp.) and emergent hydrophytes (Oryza rufipogon, Polygonum barbatum). So, all these might be the reasons for registering a high avian community composition even though these sites are unprotected and highly disturbed.

This survey shows 12 bird species (11.42%) of conservation importance in six unprotected and disturbed wetlands of Ayodhya district, Uttar Pradesh. In addition to this, species like Sarkidiornis melanotos and other raptor species listed in Appendix II of CITES are also found in these wetlands. All the species recorded in these wetlands are also listed under Schedule of Indian Wildlife (Protection) Act, 1972. Moreover, the global population trend of 39 bird species recorded from these wetlands is declining. So, from a global bird conservation point of view, the protection of these species and their habitat is of utmost importance.

On the other hand, three wetlands surveyed in this district yielded very few bird species (≤3) (Table 1) due to which they were removed from further analysis. The size of all three wetlands was less than 2 ha which was very less as compared to the other wetlands currently under study. So, the size of the wetlands might have influenced the bird diversity. This finding is well supported by Sarkar et al. (2013) who found similar results. This study also brings to the notice that though the medium and large sized wetlands in this area support sensitive species, the existence of the wetlands is itself in peril due to invasion of species like Eichhornia crassipes and anthropogenic activities such as fishing, land encroachment for fishing and agriculture, cattle grazing, fertilizer run-off, harvesting of Trapa natans, and urban development. Thus, endangering the habitat and survival of these bird species.

 

 

CONCLUSION

 

The sighting of 12 bird species of conservation importance and 39 species of birds having a declining population trend globally, highlights the significance of the medium and large sized unprotected and highly disturbed wetlands from the bird conservation point of view. The wetlands intermingled with the adjacent agricultural landscapes, orchards, plantations which created a congenial environment for resident as well as migratory birds as both of them have been reported in high numbers in the study area. But at the same time, small sized wetlands have reported very few bird species (≤3). This finding puts emphasis on the need for further research and replication of management activities like the ones taken up by the Forest Department in Samda Jheel in other potential medium and large sized unprotected wetlands of the district. So, this study acts as a reminder that medium and large sized wetlands, though isolated, disturbed and not designated as Ramsar sites, have the potential to be critical habitats for the most endangered species. Therefore, such wetlands should be given conservation and research priorities or else there is a possibility of losing these valuable water bird habitats forever as is evident from the three wetlands which yielded just three bird species.

 

 

Table 1. Brief description about the surveyed unprotected wetlands of Ayodhya district, Uttar Pradesh, India.

 

Name of wetland

Name of tehsil

Co-ordinates

Size

(ha)

Features

Species (No. of individuals) observed

Remark

1

Udaila Talab

Milkipur

26.598220 N 81.89370 E

62

This wetland is surrounded by main road on one side and agricultural land on the other side. There are aquatic plants and trees surrounding the wetland. The undulating topography has created many natural bunds in this wetland which are used as resting sites by the birds. Fishing and cattle grazing activities are carried out in this wetland. This is a stagnant water body.

92 (2381)

Data included in analysis

2

Sirsa Jheel

Milkipur

26.61740 N 81.860630 E

90

This wetland is surrounded by agricultural land and human habitation. The wetland is also surrounded by trees and bushes in its vicinity and has abundant aquatic weeds supporting aquatic zooplankton. This is a stagnant water body.

81 (1828)

Data included in analysis

3

Barun-shahganj Talab

Milkipur

26.681020 N 82.030810 E

13.3

This wetland is surrounded by human habitations on one side and agricultural land on other side and lies adjacent to state highway NH 330A. The wetland is also surrounded by trees and bushes and has abundant aquatic weeds supporting aquatic zooplankton. This wetland is used for fishing and irrigation purposes. This is a stagnant water body.

72 (1387)

Data included in analysis

4

Samda Jheel

Sohawal

26.7890 N 82.1850 E

78

This wetland is surrounded by agricultural land and is bisected by a road. The bisecting road on both the sides is lined with trees and the wetland is also surrounded with trees and bushes and has plenty of aquatic weeds. The forest department has recently developed raised platforms or bunds to provide artificial resting and nesting sites for the wetland birds. This is a stagnant water body.  

85 (2019)

Data included in analysis

5

Jagdishpur Talab

Sohawal

26.7320 N 82.0180 E

12.6

This wetland is surrounded by agricultural land on one side and human habitation on the other side. This wetland has trees planted on its periphery and has abundant aquatic weeds. The water from this wetland is used for irrigation purposes. This wetland is being encroached upon for paddy cultivation. It is used for extraction of edible nuts of Trapa natans. This is a stagnant water body. 

78 (1796)

Data included in analysis

6

Kharagpur Talab

Sohawal

26.733240 N 82.079410 E

1.10

This wetland is surrounded by agricultural fields from three sides and a village road on one side. Fishing and cattle grazing activities are carried out in this wetland. This is a stagnant water body.  

 Bubulcus ibis (8)

Vanellus indicus (4)

Data excluded from analysis

7

Kosipari-krama Nallah

Sadar

26.748530 N 82.091770 E

6.38

This wetland is surrounded by main road (Kosi-Parikrama road) on one side and Psidium guajava orchard on the other side. This wetland in some parts has high abundance of aquatic weeds and reeds, but in some areas is devoid of aquatic vegetation as it has been cleared for fishing purposes. This wetland is also used for cattle grazing and some area is being encroached upon for conversion into agricultural land. The Nallah primarily is used to dump the sewage of the city and finally meets with the Saryu river. This is a flowing water body.  

76 (1404)

Data included in analysis

8

Central Jail Talab

Sadar

26.771130 N 82.138010 E

0.69

This wetland is surrounded by the District Jail on one side, plantation on two sides. A railway track is also present on one side of this wetland creating high noise levels. This wetland is used by the locals for fishing activities. This wetland has abundant aquatic weeds. This is a stagnant water body.  

Bubulcus ibis (8)

Microcarbo niger (5)

Data excluded from analysis

9

Civil Line Talab

Sadar

26.775860 N 82.134210 E

1.75

This wetland is surrounded by human settlements (residential and commercial) on all sides creating high noise levels. This is a stagnant water body.

Bubulcus ibis (6)

Microcarbo niger (7)

Data excluded from analysis

 

Table 2. Checklist and status of avifauna recorded in unprotected wetlands of Ayodhya district, Uttar Pradesh, India

 

Order/Family/

Common name

Scientific name

Residential status

Feeding guild

Conservation status

Global status

Wetland sites

Plate No.

IUCN (2021)

CITES (2012)

IWPA (1972)

UDT

SDJ

SSJ

JDJ

KPN

BST

Accipitriformes

Accipitridae (10)

1

Black Kite

Milvus migrans (Boddaert, 1783)

R

C

LC

II

I

 

2

Black-winged Kite

Elanus caeruleus (Desfontaines, 1789)

R

C

LC

II

I

 

3

Indian Spotted Eagle

Clanga hastata (Lesson, 1831)

R

C

VU

II

I

×

×

×

 

4

Long-legged Buzzard

Buteo rufinus (Cretzschmar, 1829)

WV

C

LC

II

I

×

×

×

 

5

Oriental Honey Buzzard

Pernis ptilorhynchus (Temminck, 1821)

R

C

LC

II

I

×

 

6

Shikra

Accipiter badius (Gmelin, 1788)

R

C

LC

II

I

 

7

Steppe Eagle

Aquila nipalensis (Hodgson, 1833)

WV

C

EN

II

I

×

×

 

8

Tawny Eagle

Aquila rapax (Temminck, 1828)

R

C

VU

II

I

×

×

×

×

×

 

9

Western Marsh Harrier

Circus aeruginosus (Linnaeus, 1758)

WV

C

LC

II

I

×

×

×

 

10

White-eyed Buzzard

Butastur teesa (Franklin, 1831)

R

C

LC

II

I

×

 

Pandionidae (1)

 

11

Osprey

Pandion haliaetus (Linnaeus, 1758)

WV

C

LC

II

I

×

×

 

Anseriformes

Anatidae (15)

 

12

Bar-headed Goose

Anser indicus (Latham, 1790)

WV

O

LC

-

IV

×

×

 

13

Common Pochard

Aythya ferina (Linnaeus, 1758)

WV

O

VU

-

IV

×

×

×

×

 

14

Common Teal

Anas crecca (Linnaeus, 1758)

WV

O

LC

-

IV

?

×

×

×

×

 

15

Cotton Pygmy-goose

Nettapus coromandelianus (Gmelin, 1789)

R

O

LC

-

IV

 

16

Gadwall

Mareca strepera (Linnaeus, 1758)

WV

O

LC

-

IV

×

×

×

 

17

Garganey

Spatula querquedula (Linnaeus, 1758)

WV

O

LC

-

IV

×

×

×

 

18

Graylag Goose

Anser anser (Linnaeus, 1758)

WV

O

LC

-

IV

×

×

×

×

 

19

Indian Spot-billed Duck

Anas poecilorhyncha (Forster, 1781)

R

O

LC

-

IV

 

20

Knob-billed Duck

Sarkidiornis melanotos (Pennant, 1769)

R

O

LC

II

IV

×

×

 

21

Lesser Whistling Duck

Dendrocygna javanica (Horsfield, 1821)

R

O

LC

-

IV

 

22

Mallard

Anas platyrhynchos (Linnaeus, 1758)

WV

O

LC

-

IV

×

×

×

×

×

 

23

Northern Pintail

Anas acuta (Linnaeus, 1758)

WV

O

LC

-

IV

×

 

24

Northern Shoveler

Spatula clypeata (Linnaeus, 1758)

WV

O

LC

-

IV

×

×

 

25

Ruddy Shelduck

Tadorna ferruginea (Pallas, 1764)

WV

O

LC

-

IV

?

×

×

 

26

Tufted Duck

Aythya fuligula (Linnaeus, 1758)

WV

O

LC

-

IV

×

×

×

×

×

 

Charadriiformes

Burhinidae (2)

 

27

Eurasian Thick-knee

Burhinus oedicnemus (Linnaeus, 1758)

R

O

LC

-

IV

 

28

Great Thick-knee

Esacus recurvirostris (Cuvier, 1829)

R

C

NT

-

IV

×

×

 

Charadriidae (6)

 

29

Grey-headed Lapwing

Vanellus cinereus (Blyth, 1842)

WV

C

LC

-

IV

×

×

×

×

 

30

Kentish Plover

Charadrius alexandrinus (Linnaeus, 1758)

WV

C

LC

-

IV

×

×

×

 

31

Little Ringed Plover

Charadrius dubius (Scopoli, 1786)

R

O

LC

-

IV

 

32

Red-wattled Lapwing

Vanellus indicus (Boddaert, 1783)

R

O

LC

-

IV

?

1a

33

River Lapwing

Vanellus duvaucelii (Lesson, 1826)

R

C

NT

-

IV

 

34

Yellow-wattled Lapwing

Vanellus malabaricus (Boddaert, 1783)

R

C

LC

-

IV

 

Glareolidae (1)

 

35

Small Pratincole

Glareola lactea (Temminck, 1820)

R

I

LC

-

IV

?

×

×

×

×

 

Jacanidae (2)

 

36

Bronze-winged Jacana

Metopidius indicus (Latham, 1790)

R

O

LC

-

IV

?

1b

37

Pheasant-tailed Jacana

Hydrophasianus chirurgus (Scopoli, 1786)

R

O

LC

-

IV

 

 

 

 

 

 

Laridae (1)

 

38

River Tern

Sterna aurantia (Gray, 1831)

R

C

VU

-

IV

×

×

 

Recurvirostridae (1)

 

39

Black-winged Stilt

Himantopus himantopus (Linnaeus, 1758)

WV

C

LC

-

IV

1c

Rostratulidae (1)

 

40

Greater Painted-snipe

Rostratula benghalensis (Linnaeus, 1758)

R

O

LC

-

IV

 

Scolopacidae (8)

 

41

Common Greenshank

Tringa nebularia (Gunnerus, 1767)

WV

C

LC

-

IV

 

42

Common Redshank

Tringa totanus (Linnaeus, 1758)

WV

C

LC

-

IV

?

 

43

Common Sandpiper

Actitis hypoleucos (Linnaeus, 1758)

WV

C

LC

-

IV

 

44

Common Snipe

Gallinago gallinago (Linnaeus, 1758)

WV

O

LC

-

IV

×

×

×

×

 

45

Green Sandpiper

Tringa ochropus (Linnaeus, 1758)

WV

O

LC

-

IV

×

 

46

Little Stint

Calidris minuta (Leisler, 1812)

WV

O

LC

-

IV

×

×

×

×

×

 

47

Temminck's Stint

Calidris temminckii (Leisler, 1812)

WV

O

LC

-

IV

?

 

48

Wood Sandpiper

Tringa glareola (Linnaeus, 1758)

WV

O

LC

-

IV

×

 

Columbiformes

Columbidae (1)

 

49

Yellow-footed Green-pigeon

Treron phoenicopterus (Latham, 1790)

R

F

LC

-

IV

×

 

Coraciiformes

Alcedinidae (4)

50

Common Kingfisher

Alcedo atthis (Linnaeus, 1758)

R

C

LC

-

IV

?

 

51

Pied Kingfisher

Ceryle rudis (Linnaeus, 1758)

R

C

LC

-

IV

?

 

52

Stork-billed Kingfisher

Pelargopsis capensis (Linnaeus, 1766)

R

C

LC

-

IV

 

 

 

 

 

 

53

White-throated Kingfisher

Halcyon smyrnensis (Linnaeus, 1758)

R

C

LC

-

IV

 

Falconiformes

Falconidae (1)

 

54

Common Kestrel

Falco tinnunculus (Linnaeus, 1758)

WV

C

LC

II

IV

×

×

1g

Gruiformes

Gruidae (1)

 

55

Sarus Crane

Antigone antigone (Linnaeus, 1758)

R

O

VU

-

IV

×

1h

Rallidae (5)

 

56

Common Coot

Fulica atra (Linnaeus, 1758)

R

O

LC

-

IV

 

57

Common Moorhen

Gallinula chloropus (Linnaeus, 1758)

R

O

LC

-

IV

 

58

Purple Swamphen

Porphyrio porphyrio (Linnaeus, 1758)

R

O

LC

-

IV

?

2a

59

Watercock

Gallicrex cinerea (Gmelin, 1789)

R

C

LC

-

IV

×

 

60

White-breasted Waterhen

Amaurornis phoenicurus (Pennant, 1769)

R

O

LC

-

IV

?

2b

Passeriformes

Acrocephalidae (1)

 

61

Blyth's Reed Warbler

Acrocephalus dumetorum (Blyth, 1849)

WV

O

LC

-

IV

×

 

Alaudidae (1)

 

62

Sand Lark

Alaudala raytal (Blyth, 1845)

R

O

LC

-

IV

 

Cisticolidae (2)

 

63

Ashy Prinia

Prinia socialis (Sykes, 1832)

R

I

LC

-

IV

×

2c

64

Plain Prinia

Prinia inornata (Sykes, 1832)

R

I

LC

-

IV

×

×

2d

Dicruridae (1)

 

65

Black Drongo

Dicrurus macrocercus (Vieillot, 1817)

R

C

LC

-

IV

?

 

Estrildidae (2)

 

66

Indian Silverbill

Euodice malabarica (Linnaeus, 1758)

R

G

LC

-

IV

×

 

67

Scaly-breasted Munia

Lonchura punctulata (Linaeus, 1758)

R

O

LC

-

IV

×

 

Hirundinidae (4)

 

68

Barn Swallow

Hirundo rustica (Linnaeus, 1758)

WV

I

LC

-

IV

×

×

×

 

69

Plain Martin

Riparia paludicola (Vieillot, 1817)

R

I

LC

-

IV

×

 

70

Streak-throated Swallow

Petrochelidon fluvicola (Blyth, 1855)

R

I

LC

-

IV

 

71

Wire-tailed Swallow

Hirundo smithii (Leach, 1818)

R

I

LC

-

IV

 

Leiothrichidae (1)

 

72

Common Babbler

Argya caudata (Dumont, 1823)

R

O

LC

-

IV

×

 

Motacillidae (5)

 

73

Citrine Wagtail

Motacilla citreola (Pallas, 1776)

WV

I

LC

-

IV

×

 

74

Grey Wagtail

Motacilla cinerea (Tunstall, 1771)

WV

I

LC

-

IV

×

×

×

×

 

75

Western Yellow Wagtail

Motacilla flava (Linnaeus, 1758)

WV

I

LC

-

IV

×

 

76

White Wagtail

Motacilla alba (Linnaeus, 1758)

WV

I

LC

-

IV

×

 

77

White-browed Wagtail

Motacilla maderaspatensis (Gmelin, 1789)

R

I

LC

-

IV

 

Muscicapidae (2)

 

78

Black Redstart

Phoenicurus ochruros (Gmelin, 1774)

WV

I

LC

-

IV

×

×

 

79

Bluethroat

Luscinia svecica (Linnaeus, 1758)

WV

I

LC

-

IV

×

×

×

×

2f

Passeridae (1)

 

80

House Sparrow

Passer domesticus (Linnaeus, 1758)

R

O

LC

-

IV

×

 

Phylloscopidae (1)

 

81

Hume's Warbler

Phylloscopus humei (Brooks, 1878)

WV

I

LC

-

IV

×

×

×

×

×

 

Sturnidae (4)

 

82

Asian Pied Starling

Gracupica contra (Linnaeus, 1758)

R

O

LC

-

IV

 

83

Bank Myna

Acridotheres ginginianus (Latham, 1790)

R

O

LC

-

IV

 

84

Brahminy Starling

Sturnia pagodarum (Gmelin, 1789)

R

O

LC

-

IV

?

×

×

 

85

Common Myna

Acridotheres tristis (Linnaeus, 1766)

R

O

LC

-

IV

 

Pelecaniformes

Anhingidae (1)

 

86

Oriental Darter

Anhinga melanogaster (Pennant, 1769)

WV

O

NT

-

IV

×

 

Ardeidae (8)

87

Black-crowned Night Heron

Nycticorax nycticorax (Linnaeus, 1758)

R

O

LC

-

IV

 

88

Cattle Egret

Bubulcus ibis (Linnaeus, 1758)

R

C

LC

-

IV

 

89

Great Egret

Ardea alba (Linnaeus, 1758)

R

C

LC

-

IV

?

 

90

Grey Heron

Ardea cinerea (Linnaeus, 1758)

WV

C

LC

-

IV

?

×

×

×

2f

91

Indian Pond Heron

Ardeola grayii (Sykes, 1832)

R

C

LC

-

IV

?

 

92

Intermediate Egret

Ardea intermedia (Wagler, 1829)

R

C

LC

-

IV

×

 

93

Little Egret

Egretta garzetta (Linnaeus, 1766)

R

C

LC

-

IV

 

94

Purple Heron

Ardea purpurea (Linnaeus, 1766)

R

C

LC

-

IV

2g

Ciconiidae (3)

95

Asian Openbill

Anastomus oscitans (Boddaert, 1783)

R

C

LC

-

IV

?

1d

96

Painted Stork

Mycteria leucocephala (Pennant, 1769)

WV

C

NT

-

IV

×

×

×

1f

97

Woolly-necked Stork

Ciconia episcopus (Boddaert, 1783)

R

C

NT

-

IV

×

1e

Phalacrocoracidae (2)

98

Indian Cormorant

Phalacrocorax fuscicollis (Stephens, 1826)

WV

C

LC

-

IV

?

×

 

99

Little Cormorant

Microcarbo niger (Vieillot, 1817)

R

C

LC

-

IV

?

 

Threskiornithidae (2)

 

100

Black-headed Ibis

Threskiornis melanocephalus (Latham, 1790)

V

C

NT

-

IV

×

×

2h

101

Red-naped Ibis

Pseudibis papillosa (Temminck, 1824)

WV

C

LC

-

IV

 

Phoenicopteriformes

Podicipedidae (2)

102

Great Crested Grebe

Podiceps cristatus (Linnaeus, 1758)

WV

C

LC

-

IV

?

×

×

×

×

 

103

Little Grebe

Tachybaptus ruficollis (Pallas, 1764)

R

C

LC

-

IV

 

Strigiformes

Strigidae (2)

 

104

Jungle Owlet

Glaucidium radiatum (Tickell, 1833)

R

C

LC

-

IV

 

105

Spotted Owlet

Athene brama (Temminck, 1821)

R

C

LC

II

IV

 

IUCN: International Union for Conservation of Nature and Natural Resources; CITES: Convention on International Trade in Endangered Species of Wild Fauna and Flora; IWPA: Indian Wildlife Protection Act; R: Resident, WV: Winter Visitor, V: Vagrant; C: Carnivorous; O: Omnivorous; I: Insectivorous; F: Frugivorous; G: Granivorous; LC: Least Concern; EN: Endangered; VU: Vulnerable; NT: Near Threatened; CITES II: Appendix-II species of CITES are the ones that are not necessarily threatened now with extinction but may become so unless trade is closely controlled; IWPA I: Schedule - I species of IWPA (high priority species); IV: Schedule - IV species of IWPA (relatively low priority species); ?: Unknown; →: Stable; ↑: Increasing; ↓: Decreasing; UDT: Udaila Talab; SDJ: Samda Jheel; SSJ: Sirsa Jheel; JDJ: Jagdishpur Jheel; KPN: Kosiparikrama Nallah; BST: Barunshahganj Talab; √: Species recorded in the site; ×: Species not recorded in the site.

 

 

Table 3. Relative diversity (Rdi) of various avian families in unprotected wetlands of Ayodhya district, Uttar Pradesh, India

Avian family

Number of species recorded

Rdi value

Anatidae

15

14.29

Accipitridae

10

9.52

Ardeidae

9

8.57

Scolopacidae

8

7.62

Charadriidae

6

5.71

Rallidae

5

4.76

Motacillidae

5

4.76

Alcedinidae

4

3.81

Hirundinidae

4

3.81

Sturnidae

4

3.81

Ciconiidae

3

2.86

Burhinidae

2

1.90

Jacanidae

2

1.90

Cisticolidae

2

1.90

Estrildidae

2

1.90

Muscicapidae

2

1.90

Phalacrocoracidae

2

1.90

Threskiornithidae

2

1.90

Podicipedidae

2

1.90

Strigidae

2

1.90

Pandionidae

1

0.95

Glareolidae

1

0.95

Laridae

1

0.95

Recurvirostridae

1

0.95

Rostratulidae

1

0.95

Columbidae

1

0.95

Falconidae

1

0.95

Gruidae

1

0.95

Acrocephalidae

1

0.95

Alaudidae

1

0.95

Dicruridae

1

0.95

Leiothrichidae

1

0.95

Passeridae

1

0.95

Phylloscopidae

1

0.95

Anhingidae

1

0.95

 

 

Table 4. Measurements of avian diversity and richness at unprotected wetland sites of Ayodhya district, Uttar Pradesh, India.

Wetland sites

Species richness

Shannon-Weiner Diversity Index (SDI)

Margalef's Richness Index (MRI)

Simpson's Dominance Index

Pielou's Evenness Index (PEI)

Udaila Talab

92

3.86

26.94

0.03

0.85

Samda Jheel

85

3.82

25.41

0.03

0.86

Sirsa Jheel

81

3.80

24.52

0.03

0.86

Jagdishpur Jheel

78

3.63

23.66

0.05

0.83

Kosiparikrama Nallah

76

3.62

23.82

0.03

0.83

Barunshahganj Talab

72

3.55

22.59

0.04

0.83

 

 

Table 5. Sorenson’s Similarity Index of avian species between selected unprotected wetland sites of Ayodhya district, Uttar Pradesh, India.

Wetland sites

Udaila talab

Samda Jheel

Sirsa Jheel

Jagdishpur Jheel

Kosiparikrama Nallah

Barunshahganj Talab

Udaila talab

0.000

 

 

 

 

 

Samda Jheel

0.915

0.000

 

 

 

 

Sirsa Jheel

0.890

0.880

0.000

 

 

 

Jagdishpur Jheel

0.847

0.798

0.830

0.000

 

 

Kosiparikrama Nallah

0.810

0.795

0.803

0.766

0.000

 

Barunshahganj Talab

0.817

0.803

0.850

0.853

0.824

0.000

 

For figures & images - - click here for full PDF

 

REFERENCES

 

Ali, S. & S.D. Ripley (1987). Compact handbook of the birds of India and Pakistan together with those of Bangladesh, Nepal, Bhutan and Sri Lanka. Oxford University Press, Delhi, 737 pp.

Basavarajappa, S. (2006). Avifauna of agro-ecosystems of Maidan area of Karnataka. Zoos’ Print Journal 21(4): 2217–2219. https://doi.org/0.11609/JoTT.ZPJ.1277.2217-9

Bassi, N., M.D. Kumar, A. Sharma & P. Pardha-Saradhi (2014). Status of wetlands in India: a review of extent, ecosystem benefits, threats and management strategies. Journal of Hydrology: Regional Studies 2: 1–19. https://doi.org/10.1016/j.ejrh.2014.07.001

Behera, M.D., V.S. Chitale, A. Shaw, P.S. Roy & M.S.R. Murthy (2012). Wetland monitoring, serving as an index of Land use change – a study in Samaspur Wetlands, Uttar Pradesh. Journal of Indian society of Remote Sensing 40(2): 287–297. https://doi.org/10.1007/s12524-011-0139-6

Bibby, C.J., D.A. Hill, N.D. Burgess & S. Mustoe (2000). Bird census techniques. Academic Press, London, 302 pp.

Blackenberg, M., M.C. Mlambo, D. Parker, S.N. Motitsoe & C. Reed (2020). Protected and un-protected urban wetlands have similar aquatic macroinvertebrate communities: A case study from the Cape Flats Sand Fynbos region of southern Africa. PloS One 15(5): e0233889. https://doi.org/10.1371/journal.pone.0233889

 Chopra, G. & S.K. Sharma (2012). Avian biodiversity in and around major wetlands of ‘‘lower shivalik foothills’’, India. Nature and Science 10(7): 86–93.

CITES (Convention on International Trade in Endangered Species of Wild Fauna and Flora) (2012). Checklist of Convention on International Trade in Endangered Species of Wild Fauna and Flora. CITES, Geneva, Switzerland. http://www.cites.org. Accessed on 02 January 2021.

Colwell, M.A. & O.W. Taft (2000). Waterbird Communities in Managed Wetlands of Varying Water Depth. Waterbirds 23(1): 45–55. https://www.jstor.org/stable/4641109

Custer, T.W. & R.G. Osborn (1977). Wading birds as biological indicators: 1975 Colony Survey. US Fish and Wildlife Service, Washington D.C.

eBird (2021). eBird Uttar Pradesh, India. https://ebird.org/region/IN-UP?yr=all Accessed on 06 March 2021.

Gopal, K., H.O. Verma & S. Tripathi (2015). Water quality monitoring of Sur Sarovar (Keetham) Lake, Agra (Uttar Pradesh). Journal of Ecophysiology and Occupational Health 15(3&4): 95–103.

Grimmett, R., C. Inskipp & T. Inskipp (2011). Birds of the Indian Subcontinent. Oxford University Press & Christopher Helm, London, 480 pp.

Helmers, D.L. (1992). Western Hemisphere Shorebird Reserve Network. Manomet, MA, 58 pp.

IUCN (2021). The IUCN Red List of Threatened Species. Version 2021-3. http://www.iucnredlist.org.

IWPA (1972). The Indian Wildlife (Protection) Act, 1972 (as amended up to 1993). Ministry of Environment, Forest and Climate Change, Govt. of India, Delhi. http://www.envfor.nic.in/legis/wildlife/wildlife1.html. Accessed on 02nd January 2021.

Jha, K.K. (2013). Aquatic food plants and their consumer birds at
Sandi Bird Sanctuary, Hardoi, Northern India. Asian Journal of Conservation Biology 2(1): 30–43.

Kumar, A., J.P. Sati, P.C. Tak & J.R.B. Alfred (2005). Handbook on Indian Wetland Birds and their Conservation. Zoological Survey of India, Kolkata, India, 468 pp.

Kumar, P. & A. Sharma (2018). Diversity and status of avifauna in man-made sacred ponds of Kurukshetra, India. Journal of Threatened Taxa 10(9): 12173–12193. https://doi.org/10.11609/jott.3729.10.9.12173-12193

Kumar, P. & S.K. Gupta (2009). Diversity and abundance of wetland birds around Kurukshetra, India. Our Nature 7: 212–217.

Kumar, P., D. Rai & S.K. Gupta (2016). Wetland bird assemblage in rural ponds of Kurukshetra, India. Waterbirds 39(1): 86–98. https://doi.org/10.1675/063.039.0111  

Kumar, S. (2018). Cultural landscape and heritage of Ayodhya-Faizabad: A geographical analysis. Ph.D. Thesis submitted to Department of Geography, Banaras Hindu University, Varanasi, Uttar Pradesh.

KVK (2021). Krishi Vigyan Kendra, Ayodhya. https://ayodhya.kvk4.in/district-profile.html Accessed on 02 January 2021.

Margalef, R. (1958). Temporal succession and spatial heterogeneity in phytoplankton, pp. 323–347. In: Buzzati-Traverso, A.A. (ed.). Perspectives in Marine Biology. University of California Press, Berkeley, 621 pp.

Mazumdar, S. (2019). Composition of avian communities in a human-modified wetland Okhla Bird Sanctuary, India: with notes on conservation initiatives. Proceedings of Zoological Society 72: 319–333. https://doi.org/10.1007/s12595-017-0239-6

Murkin, H.R. & J.A. Kadlec (1986). Relationships between waterfowl and macroinvertebrate densities in a northern prairie marsh. Journal of Wildlife Management 50(2): 212–217. https://doi.org/10.2307/3801899

NWA (2010).  Uttar Pradesh, SAC/RESA/AFEG/NWIA/ATLAS/12/2010, National Wetland Atlas. Space Applications Centre, ISRO, Ahmedabad, India, 372 pp.

Pielou, E.C. (1966). The measurement of diversity in different types of biological collections. Journal of Theoretical Biology 13: 131-144. https://doi.org/10.1016/0022-5193(66)90013-0

Praveen, J., R. Jayapal & A. Pittie (2020). Taxonomic updates to the checklists of birds of India, and the South Asian region – 2020. Indian Birds 16(1): 12–19.

Rajashekara, S. & M.G. Venkatesha (2010). The diversity and abundance of waterbirds in lakes of Bangalore city, Karnataka, India. Biosystematica 4(2): 63–73.

Rani, R., R. Gautam & R.K. Gautam (2009). Floristic survey of medicinal plants in Sur Sarovar wetland, Kheetam, Agra, India. Journal of Applied and Natural Science 1(2): 196–200.

Reddy, C.S., M. Rangaswamy, C. Pattanaik & C.S. Jha (2009). Invasion of alien species in wetlands of Samaspur Bird Sanctuary, Uttar Pradesh, India. Asian Journal of Water, Environment and Pollution 6(3): 43–50.

Sarkar, B., P. Hazra, S.P. Kumar, P. Ghosh, A. Banerjee & T.N. Khan (2013). Habitat attributes and waterbird-use of four wetlands in Manas National Park, Assam, India. Proceedings of Zoological Society. https://doi.org/10.1007/s12595-013-0074-3

Saygili, F., N. Yigit & S. Bulut (2011). The spatial and temporal distributions of waterbirds in Lakes Aksehir-Eber and Lake Koycegiz in western Anatolia, Turkey - a comparative analysis. Turkish Journal of Zoology 35(4): 467–480.

Shannon C.E. & W.W. Wiener (1963). The Mathematical Theory of Communications. University of Illinois, Urbana, USA.

Sharma, N. (2007). Butterflies of Sur Sarovar Bird Sanctuary, Keetham, Agra (Uttar Pradesh, India). Records of Zoological Survey of India 107(2): 103–112.

Shine, C. & C. Klemm (1999). Wetlands, Water and the Law. Using law to advance wetland conservation and wise use. IUCN, Gland, Switzerland, Cambridge, UK and Bonn, Germany, 330 pp.

Simpson, E.H. (1949). Measurement of diversity. Nature 163: 688.

Sorenson, T. (1948). A method of establishing groups of equal amplitude in plant sociology based on similarity of species and its application to analyses of the vegetation on Danish commons. Biologiske Skrifter/ Kongellege Danske Videnskabernes Selskab 5

Sundar, K.S.G. & S. Kittur (2012). Methodological, temporal and spatial factors affecting modeled occupancy of resident birds in the perennially cultivated landscape of Uttar Pradesh, India. Landscape Ecology 27: 59–71. https://doi.org/10.1007/s10980-011-9666-3

Sundar, K.S.G. & S. Kittur (2013). Can wetlands maintained for human use also help conserve biodiversity? Landscape-scale patterns of bird use of wetlands in an agricultural landscape in north India. Biological Conservation 168: 49–56. https://doi.org/10.1016/j.biocon.2013.09.016

Tak, P.C., J.P. Sati & A.N. Rizvi (2010). Status of waterbirds at Hathnikund Barrage wetland, Yamunanagar District, Haryana, India. Journal of Threatened Taxa 2(4): 841–844. https://doi.org/10.11609/JoTT. o2200.841-4   

Torre-Cuadros, M.D.L.A.L., S. Herrando-Perez & K.R. Young (2007). Diversity and structure patterns for tropical montane and premontane forests of central Peru, with an assessment of the use of higher-taxon surrogacy. Biodiversity and Conservation 16: 2965– 2988. https://doi.org/10.1007/s10531-007-9155-9

TWI (2020). The Wetlands Initiative. What is a Wetland? http://www.wetlands-initiative.org/what-is-a-wetland. Downloaded on 17 December 2020.

Urfi, A.J. (2003). The birds of Okhla barrage bird sanctuary, Delhi, India. Forktail 19: 39–50.

Woodward, R.T. & Y-S. Wui (2001). The economic value of wetland services: a meta-analysis. Ecological Economics 37: 257–270. https://doi.org/10.1016/S0921-8009(00)00276-7

Yashmita-Ulman & M. Singh (2021). Bird composition, diversity and foraging guilds in agricultural landscapes: A case study from eastern Uttar Pradesh, India. Journal of Threatened Taxa 13(8): 19011–19028. https://doi.org/10.11609/jott.7089.13.8.19011-19028