Jin-Ming Zhao, Li-Zhi Zhou. 2018: Area, isolation, disturbance and age effects on species richness of summer waterbirds in post-mining subsidence lakes, Anhui, China. Avian Research, 9(1): 8. DOI: 10.1186/s40657-018-0101-1
Citation: Jin-Ming Zhao, Li-Zhi Zhou. 2018: Area, isolation, disturbance and age effects on species richness of summer waterbirds in post-mining subsidence lakes, Anhui, China. Avian Research, 9(1): 8. DOI: 10.1186/s40657-018-0101-1

Area, isolation, disturbance and age effects on species richness of summer waterbirds in post-mining subsidence lakes, Anhui, China

Funds: 

the National Natural Science Foundation of China 31472020

More Information
  • Corresponding author:

    Zhou Li-Zhi, zhoulz@ahu.edu.cn; zhoulz2009@qq.com

  • Received Date: 28 Sep 2017
  • Accepted Date: 06 Mar 2018
  • Available Online: 24 Apr 2022
  • Publish Date: 08 Mar 2018
  • Background 

    The species–area relationship is one of the best documented patterns in community ecology. Factors influencing species–area relationship are still not well understood. Since the proposal of the equilibrium theory of island biogeography, many studies have tested the effects of area and isolation, estimating effects of disturbance and patch age were scarce and should also be important bearing.

    Methods 

    We investigated summer waterbird species richness in 38 post-mining subsidence lakes in Huainan and Fuyang, Anhui, China, May 25–June 12, 2016. We examined the effects of lake area, isolation (distance to natural water bodies), aquaculture disturbance, lake age and lake state (still sinking or not sinking) on summer waterbird species richness with multivariable linear regression method and model selection method.

    Results 

    Our results from multivariable linear regression and model selection were consistent, which showed that species richness was positively related with lake area and negatively related with isolation. Aquaculture disturbance negatively influenced species richness. Highest species richness were found in lakes under intermediate intensity of aquaculture activities with area less than 100 ha and lakes under low intensity of aquaculture activities with area greater than 100 ha. Lake age and lake state had no significant effects on species richness.

    Conclusions 

    Species richness was most related with lake area, aquaculture disturbance, and isolation, with lake area had a positive effect, while aquaculture activities and isolation had a negative effect. What's more, aquaculture activities significantly changed the slope of species–area relationship and might impede us finding a relationship between species richness and lake age.

  • Birds have been widely considered as an important tool in biodiversity conservation planning and monitoring (Kremen 1992; Chettri et al. 2001; Bregman et al. 2014) and for identifying conservation actions. Birds and their diversity provide strong bio-indication signals (Vielliard 2000; Bhatt and Joshi 2011; Urfi 2011; Bregman et al. 2014), and stand as surrogates for the health of ecosystem and status of biodiversity overall (Chettri 2010; Pakkala et al. 2014; Pierson et al. 2015). Anthropogenic drivers of change have fomented large-scale habitat destruction, fragmentation and degradation, necessitating an assessment of the impacts of such change on birds (Wiens 1995; Chettri et al. 2001; McLaughlin 2011; Bregman et al. 2014). Understanding diversity of bird communities in different habitats is essential to understand the community structure and niche relationships, as well to delineate the importance of regional or local landscapes for avian conservation (Kattan and Franco 2004; Chettri 2010; Singh et al. 2013).

    The Eastern Himalaya is a meeting ground for the Indo-Malayan, Palaearctic, and Sino-Japanese biogeographical realms. The area is known for diverse ecological and altitudinal gradients (CEPF 2005, 2007) and provides habitat for rich diversity of flora and fauna, including birds of the Oriental region (Crosby 1996). The Eastern Himalaya has been identified as a Priority I Endemic Bird Area (Birdlife International 2001), supporting 22 restricted-range bird species of which 19 are endemic to the region (Stattersfield et al. 1998; Jathar and Rahmani 2006; Acharya and Vijayan 2010). The region also represents one of the largest concentrations of globally threatened birds in Asia (Acharya and Vijayan 2010).

    The Kangchenjunga Landscape (KL) is a transboundary landscape shared by Bhutan, India and Nepal, and one of the biologically richest landscapes in the Eastern Himalaya (Yonzon 2000; Chettri et al. 2008; ICIMOD et al. 2017). Located in the Himalayas, one of the 36 Global Biodiversity Hotspots, the landscape is one of the richest in terms of biodiversity, including birds. With about 43% of the total geographical area of Nepal and 54% of Bhutan, the landscape is reported to have almost equal number of birds as Bhutan and two-thirds of Nepal. In addition, with 22 Important Bird and Biodiversity Areas (IBAs) and 19 protected areas (ICIMOD et al. 2017), the landscape has the highest number of protected areas for biodiversity conservation and it is identified as one of the priority areas for biodiversity conservation in the Himalayan region (CEPF 2005). It encompasses a part of eastern Nepal; Sikkim and a part of West Bengal in India and the western and southwestern parts of Bhutan (Fig. 1). The KL, being designated through a consultative process (from 2012 to 2015) and endorsed by the governments of Bhutan, India and Nepal, includes an area over 25, 000 km2 that surrounds Mount Kangchenjunga, the third highest mountain in the world (ICIMOD et al. 2017). Shared area by country is presented in Table 1.

    Figure  1.  The Kangchenjunga Landscape
    Table  1.  The Kangchenjunga Landscape area by country and percentage of total area
    Country Area (km2)* Percentage of total KL area* (%) Total number of species Number of threatened species
    Bhutan 5834 23 210 4
    India 14, 062 56 585 39
    Nepal 5190 21 342 15
    Total 25, 086 100
    *Source ICIMOD et al. (2017), other data from this study
     | Show Table
    DownLoad: CSV

    The KL is situated between 26°21′40.49ʺ-28°7′51.25ʺN and 87°30′30.67ʺ-90°24′31.18ʺE. The KL's altitudinal range extends from 50 m a.s.l. in the south to 8586 m a.s.l.—the height of Mount Kangchenjunga. Based on its extreme altitudinal variation, the vegetation in the KL ranges widely: tropical, subtropical, warm temperate, cool temperate, subalpine, and alpine zones (Chaudhary et al. 2015; Uprety et al. 2016; ICIMOD et al. 2017). The different vegetation zones of the KL support a wide diversity of flora and fauna. More than 5000 species of flowering plants including more than 500 varieties of orchid and 40 varieties of rhododendron are recorded from the region (Kandel et al. 2016). Of the 160 recorded mammal species, four are endemic to this region (Chettri et al. 2008).

    The KL supports wide diversity of birds, many of them endemic to the region (Chettri et al. 2008). Of the 19 endemic bird species of the Eastern Himalaya, 10 are found in Sikkim (India) alone. The KL also represents a relatively high number of threatened bird species: Of the 78 threatened birds on the Indian Sub-continent, 17 (one endangered, three critically endangered and 13 vulnerable) occur in Sikkim (Acharya and Vijayan 2010). However, like many other landscapes worldwide, the KL is experiencing intense disturbances due to anthropogenic pressures such as logging, firewood collection, livestock grazing, development activities, and a growing tourism industry that may jeopardize its rich avifaunal diversity (Chettri et al. 2002, 2007a, b). These global changes also pose acute threats to biodiversity of the Himalayan landscape as they are rich in endemic species that have narrow and restricted ranges of distribution (Chettri 2010). Hence, documentation of bird communities, their patterns of distribution, habitat preferences, threats and conservation practices and policies are crucial for developing future conservation measures in the KL.

    Documentation of bird communities in the KL dates back to 19th century and many preliminary accounts on birds from the region are extant (Bulger 1869; Bulger 1869; Blandford 1871, 1872; Gammie 1877; Brooks 1880; Ludlow and Kinnear 1937a, b; Mills 1944; Maclaren 1947, 1948; Sen 1948, 1957; Law 1953). However, despite these excellent volumes, information on birds in the KL are still limited and skewed in many respects. For instance, some areas including Sikkim and some protected areas (e.g., Kanchenjunga Conservation Area and Buxa Tiger Reserve) have been intensively catalogued while some protected areas (e.g., Mahananda Wildlife Sanctuary and Maenam Wildlife Sanctuary) lack even basic information such as species checklists. Furthermore, many literature in KL birds is not easily accessible as they are distributed among wide variety of sources. For example, unpublished student's theses held in libraries of universities and unpublished reports prepared by organizations working in the KL. For these reasons, we attempt to consolidate the knowledge on birds reported and documented from the KL, understand their distribution, identify conservation and management challenges, and note directions for future research.

    We collected information using secondary sources run through a systematic review process. We reviewed published journals articles and books on the birds reported from the KL, and conducted several systematic web-based searches. Using 'Google Scholar, ' we searched literature using specific search terms including 'birds', 'avifauna', and 'Bhutan', 'Sikkim', 'Darjeeling', 'Jalpaiguri', 'India', 'Nepal' and 'Kangchenjunga Landscape'. Since the literature searches were done in 2017, we collected literature published till 2016. To account for publications that were not retrieved using these search terms, we searched literature using the name of protected areas found within the landscape. We also conducted additional searches for technical reports, student theses, government publications, agency reports, websites and databases of ongoing projects, and synthesis papers or book chapters. For practicality, we included only English language literature. A total of 119 literature related to the birds of the KL were collected and considered for the review. To enlist the birds of the KL, we referred 23 literature whose references are given against each bird species in the database of the birds. The list of literature and the database of birds from the KL are provided as Additional files 1 and 2.

    With the collated material, we prepared a database of bird species found in each country, noting each species by common name, Latin name, genus, species, order, family, distribution (by altitude in meters), habitat preferences, IUCN threat status, and country level protection. Oriental Bird Club codes as given by Inskipp et al. (1996) and reference of a literature for each species are also included in the database. The precision of our species identification is dependent on the clarity and presentation of the original sources. We verified nomenclature and conservation statuses from the International Union for the Conservation of Nature's (IUCN) online source (http://www.iucnredlist.org/) as well as in Inskipp et al. (1996). We used the altitudinal ranges and habitat preferences based on Grimmett et al. (1998). For some of the bird species that were not found in Grimmett et al. (1998), we searched in the IUCN's online source (http://www.iucnredlist.org/) to fill those gaps. For additional classification, we used five major altitudinal zones of the KL considering different zonation reported by Chaudhary et al. (2015), Uprety et al. (2016) and simplified to make distinct zones as also used by Ali (1962) namely (1) tropical (2) subtropical (3) temperate (4) subalpine and (5) alpine. To bring clarity, we combined warm temperate and cool temperate into one broad category as a temperate zone. Although it is difficult to confine altitudinal range of a bird due to its movement along large elevational gradient, we considered elevation range of individual species as reported in the literature for analysis. The habitat preference of each species has been sub-divided into eight categories: forest, wetland, scrub, cultivation, semi-desert, grassland, around habitation and open country (Grimmett et al. 1998). Finally, we analyzed the data to look into the patterns of distribution and identify habitat preferences of the general and threatened species.

    Our review resulted in 119 literature on birds of the KL. Of these, 92 are journal articles and rest are books, book chapters, government documents and institutional reports (Additional file 1). Majority of the bird studies in the KL are from India (83%) followed by studies from Nepal (9%) and Bhutan (8%). In India, 43% of the studies are carried out in Sikkim alone, while 57% are carried out in North Bengal, including Darjeeling, Jalpaiguri and Alipurduar districts. In Nepal, majority of the studies (71%) are carried out in the Kanchenjunga Conservation Area. This indicate that the bird studies in the KL skew to several specific areas or protected areas such as Sikkim and the Kanchenjunga Conservation Area.

    Of the 92 journal articles, 57% are checklists that have used observation as a methodology to enlist the bird species. Around 26% are focused on the ecological research of the specific bird species. Around 17% of the studies are systematic investigation on species richness that have used point count method.

    We collated a dataset of 618 bird species belonging to 19 orders and 77 families. This indicates that the KL is one of the richest areas in bird diversity in the Himalayan region. Passeriformes is the most dominant order, comprising 62% of the total records. Falconiformes is the second highest order, but only 8% of the total records. Figure 2 shows the taxonomic distribution of the dataset by order. Supporting the local, regional and global trends, the landscape showed higher proportion of passerine birds as also revealed by Ali (1962), Inskipp et al. (1996) and Fjeldså et al. (2012).

    Figure  2.  Taxonomic distribution of the birds in the KL by order

    Among families, Muscicapidae (26 genera and 71 species) emerges as the most diversely represented family, followed by Sylviidae (26 genera and 50 species), Accipitridae (19 genera and 36 species) and Fringillidae (11 genera and 30 species). Other species rich families include Corvidae (14 genera and 29 species), Timaliidae (11 genera and 26 species) and Picidae (14 genera and 23 species). The dataset includes 22 families representing only one genus and one species each (see Fig. 3 for those bird families with more than 10 species in the KL). Narwade et al. (2011) also found highest number of bird species from the family Muscicapidae in a study carried out in the birds of Northeast India.

    Figure  3.  Bird families with number of genera and species reported in the Kangchenjunga Landscape

    Out of 618 bird species in the KL, the region harbors 41 species (7%) that are globally threatened and are categorized according to the terms used on the IUCN Red List. Among these 41, five species are "critically endangered": Baer's Pochard (Aythya baeri), Bengal Florican (Houbaropsis bengalensis), Red-headed Vulture (Sarcogyps calvus), Slender-billed Vulture (Gyps tenuirostris) and White-rumped Vulture (Gyps bengalensis). Three species are "endangered": Lompobattang Flycatcher (Ficedula bonthaina), Saker Falcon (Falco cherrug) and Steppe Eagle (Aquila nipalensis). Nineteen species (0.81% of the total species listed) are considered 'vulnerable.' And fourteen (2.27%) are categorized as 'near threatened'. The remaining 577 species (93.37%) belong the category 'least concern' (Table 2).

    Table  2.  Threat status of birds of the Kangchenjunga Landscape
    Threat status Number of species Percentage (%)
    Critically endangered 5 0.81
    Endangered 3 0.49
    Vulnerable 19 3.07
    Near threatened 14 2.27
    Least concern 577 93.37
     | Show Table
    DownLoad: CSV

    The conservation policies of Bhutan, India, and Nepal, have provided protection to a number of bird species that reside in the KL. Among the nationally protected bird species of Bhutan, Common Raven (Corvus corax), Himalayan Monal (Lophophorus impejanus) and Rufous-necked Hornbill (Aceros nipalensis) are found in the landscape. There are 22 bird species in the KL that are protected by the government of India. Five species of birds, Satyr Tragopan (Tragopan satyra), Himalayan Monal, Great Hornbill (Buceros bicornis), Bengal Florican, and Black Stork (Ciconia nigra), are found in the KL that are protected by the government of Nepal.

    Of all the birds documented in the KL, 95% can be found in India, 55% in Nepal, and 34% in Bhutan. Similarly, of the total 41 threatened bird species present in the KL, 95% of these can be found in India, 37% in Nepal, and 10% in Bhutan (Table 1). The highest number of bird species in India followed by Nepal and Bhutan could be attributed to the largest part of the landscape area being covered by the KL-India (56.3%) followed by the KL-Nepal (23%) and the KL-Bhutan (21%).

    Most KL bird species (24%) can be found in the tropical zone below 1000 m a.s.l. (Fig. 4) and 19% are found in the altitudinal zones from tropical to subtropical (0-2000 m a.s.l.) (see Fig. 4 for a comprehensive representation of the birds in relation to elevation). The results are in line with the trend of having less species diversity as we move higher elevation as also revealed by Acharya et al. (2011), Chettri et al. (2001) and Chettri (2010).

    Figure  4.  Distribution of birds at different altitudinal zones in the Kangchenjunga Landscape

    Sixty-three percent of KL bird species inhabit forests, while 16% can be found in wetlands (Fig. 5). Approximately 11% of the species were found in scrub land and just 15 was found in open country. If we consider only threatened bird species, 34% inhabit forests and 34% inhabit wetlands, 12% live in grasslands. Three species each inhabit scrub land, open country, and around habitation areas.

    Figure  5.  Number of bird species occurring in different habitats. Figures are not cumulative because several species are found in more than one habitat types

    There are 22 IBAs in the KL (see Table 4 and Fig. 6 for a detailed description of the IBAs). Among them, three are in Nepal, five in Bhutan, and 14 in India (Ganguli-Lachungpa et al. 2007; Chaudhary et al. 2015; Birdlife International 2016). These IBAs provide shelter to a number of endemic bird species such as Chestnut-breasted Partridge (Arborophila mandellii), Rusty-bellied Shortwing (Brachypteryx hyperythra) and White-naped Yuhina (Yuhina bakeri), restricted range species like Hoary-throated Barwing (Actinodura nipalensis) and Ward's Trogon (Harpactes wardii) that are endemic to the KL. These IBAs also provide either permanent or temporary habitats for a number of threatened bird species including the critically endangered and globally threatened species. Globally significant bird species that are present in the IBAs of the KL are given in Table 3.

    Table  3.  Important Bird and Biodiversity Areas in the Kangchenjunga Landscape
    IBA* Country Protected area Significant bird species
    Jigme Khesar Strict Nature Reserve (BT002) (formerly known as Toorsa Strict Nature Reserve) Bhutan Chestnut-breasted Partridge
    Wood Snipe Rufous-necked Hornbill
    Samtse (BT003) Bhutan Rufous-necked Hornbill
    Chele La (BT004) Bhutan Wood Snipe
    Paro wetlands (BT005) Bhutan Wood Snipe
    Kamji (BT007) Bhutan Rufous-necked Hornbill
    Lava-Neora Valley National Park (IN322) India Eastern-imperial Eagle
    Pale-capped Pigeon
    Rufous-necked Hornbill
    Black-breasted Parrotbill Beautiful Nuthatch
    Mahananda Wildlife Sanctuary (IN323) India White rumped Vulture
    Slender-billed Vulture
    Bengal Florican
    Swamp Francolin
    Lesser Adjutant
    Rufous-necked Hornbill
    Black-breasted Parrotbill
    Singhalila National Park (IN325) India Chestnut-breasted Partridge
    Greater-spotted Eagle
    Wood Snipe
    Beautiful Nuthatch
    Barsey Rhododendron Sanctuary (IN327) India Pallas's Fish-eagle Black-breasted Parrotbill
    Dombang Valley-Lachung-Lema-Tsungthang (IN328) India Wood Snipe
    Beautiful Nuthatch
    FambongLho Wildlife Sanctuary-Himalayan Zoological Park-Ratey Chu Reserve Forest (IN329) India White rumped Vulture
    Slender-billed Vulture
    Chestnut-breasted Partridge
    Rufous-necked Hornbill
    Beautiful Nuthatch
    Khangchendzonga National Park and Biosphere Reserve (IN330) India Baer's pochard
    Pallas's Fish-eagle
    Black-breasted Parrotbill
    Kyongnosla Alpine Sanctuary-Tsomgo-Tamze-Chola Complex (IN331) India Greater-spotted Eagle
    Pallas's Fish-eagle
    Wood Snipe
    Lhonak Valley (IN332) India Wood Snipe
    Black-necked Crane
    Lowland forests of South Sikkim (IN333) India White rumped vulture
    Slender-billed Vulture
    Chestnut-breasted Partridge
    Rufous-necked Hornbill
    Grey-crowned Prinia
    Slender-billed Babbler
    Black-breasted Parrotbill
    Beautiful Nuthatch
    Maenam Wildlife Sanctuary-Tendong Reserve Forest (IN334) India Chestnut-breasted Partridge
    Blyth's Tragopan
    Greater-spotted Eagle
    Rufous-necked Hornbill
    Beautiful Nuthatch
    Pangolakha Wildlife Sanctuary-Zuluk-Bedang Tso-Natula Complex (IN335) India Chestnut-breasted Partridge
    Greater-spotted Eagle
    Pallas's Fish-eagle
    Wood Snipe
    Rufous-necked Hornbill
    Grey-crowned Prinia
    Slender-billed Babbler Black-breasted Parrotbill
    Tso Lhamo Plateau-Lashar-Sebu La-Yumesandong Complex (IN336) India Greater-spotted Eagle
    Wood Snipe
    Black-necked Crane
    Yumthang-Shingba Rhododendron Wildlife Sanctuary (IN337) India Wood Snipe
    Kangchenjunga Conservation Area (NP010) Nepal Wood Snipe
    Spiny Babbler
    Mai Valley Forests (NP015) Nepal White Rumped Vulture
    Slender-billed Vulture
    Red-headed Vulture
    Wood Snipe
    Greater-spotted Eagle
    Lesser Adjutant
    Spiny Babbler
    Tamur Valley and Watershed (NP026) Nepal Spiny Babbler
    *Numbers indicate IBA code numbers. The Latin names of all these species are in Additional file 2
     | Show Table
    DownLoad: CSV
    Figure  6.  Map showing IBAs within the Kangchenjunga Landscape
    Table  4.  A summary of national policies, laws and international conventions of the countries that share the Kangchenjunga Landscape (in chronological order)
    Bhutan India Nepal
    Some national policies National Forest Policy 1974 Forest Policy 1952 New Forest Policy 1978
    Master plan for forest development 1990 National conservation Strategy and Policy Statement, India 1992 National Conservation Strategy 1988 which is later revisited as Nature Conservation National Strategic Framework for Sustainable development (2015-2030)
    Biodiversity Action plan 1994 National Forest Policy 1998 Environment Policy and action Plan 1993
    National Environment Strategy ("The Middle Path") 1998 National Wildlife Action Plan (2002-2016) Tenth Plan (2002-2007)
    Biodiversity Action Plan 2002 National Action Plan on Climate Change 2008 Nepal Biodiversity Strategy 2002
    Revision of Forest Policy draft 2010 National Biodiversity Strategy and Action Plan 2009 Sustainable Development Agenda for Nepal 2003
    Nepal Biodiversity Strategy Implementation Plan 2006
    National Bio-safety framework 2006
    Three-year Interim Plan (2007-2010)
    National Agriculture Policy 2004
    Rangeland Policy 2012
    National Wetland Policy 2012
    Vulture Conservation Action Plan (2009-2013)
    National Biodiversity Strategy and Action Plan (2014-2020)
    Some national laws Bhutan Forest Act 1969 Indian Forest Act 1927 and its successive amendments 1980 Nepal Legal Code "the muliki ain" 1854
    Forest and Nature Conservation Act 1995 Wildlife (Protection) Act 1972 (last amended in 2013) Nepal Forest Nationalization Act 1957
    Environment Assessment Act 2002 Environment Protection Act 1986 Nepal Forest Act 1962 its amendments 1968
    Forest and Nature Conservation Rules Volumes I & II 2002 Panchayati Raj (Extension to Scheduled Areas) Act 1996 Forest Act 1993
    National Biodiversity Act 2003 Biological Diversity Act 2002 National Parks and Wildlife Conservation Act, Nepal 1972 and amendment 2002
    Land Act of Bhutan 2007
    National Environment Protection Act 2007
    International conventions Ramsar Convention 1971 Ramsar Convention 1971 Ramsar convention 1971
    United Nations Convention on International Trade in Endangered Species of Wild Flora and Fauna (CITES) 1975 UNESCO's Man and Biosphere Programme 1971 CITES
    Convention on Biological Diversity (CBD) 1992 CITES 1975 Bonn convention 1983
    United Nations Framework Convention on Climate Change (UNFCCC) 1992 Convention on the Conservation of Migratory Species of Wild Animals (Bonn Convention) 1983 CBD 1992
    United Nations Convention to Combat Desertification (UNCCD) 1994 CBD 1992 UNFCCC 1992
    UNFCCC 1992 UNCCD 1994
    UNCCD 1994 Kyoto Protocol to the UNFCCC
    IBAs 23 (8 within protected area network) 465 (279 with in protected areas network and 16 are listed as Ramsar sites) 27 (13 within protected areas network)
     | Show Table
    DownLoad: CSV

    Despite the global biological significance, the region faces numerous challenges for biodiversity conservation and sustainable development. While some of these issues are at the local and national levels, others occur at the transboundary level. Habitat loss and fragmentation pose major factors in the decline in population of threatened and endemic birds in the Himalaya and elsewhere (Crosby 1996; Chettri et al. 2001, 2005; Pandit et al. 2007). Various human activities common in the KL such as deforestation, forest encroachment for expansion of agricultural land and overgrazing affect the bird community structure in the landscape (Chettri et al. 2005). Many ethnic communities in the forested highlands of the KL continue to clear forested land and practice slash-and-burn agriculture (shifting cultivation), which drives habitat loss at higher altitudes, particularly in KL-Nepal where the practice is considered illegal (Inskipp et al. 2008; Aryal et al. 2010). Slash-and-burn agriculture with lesser annual cycle has a significant negative impact on bird diversity (Inskipp et al. 2008).

    Hunting plays a significant role in the culture, tradition and subsistence economies of the people living in the KL and is still commonly practiced in the region (Inskipp et al. 2008; Sathyakumar et al. 2010; Inskipp et al. 2013). It poses a serious threat to game birds (Galliformes), water birds, and large- bodied species such as hornbills (Keane et al. 2005; Velho et al. 2012). Hunting practices also imperil a number of threatened species, including Satyr Tragopan and Himalayan Monal. For instance, Himalayan Monal has been hunted in the Kanchenjunga Conservation Area for generations and in a survey conducted by Inskipp et al. (2008) only one individual species was located despite an extensive suitable habitat. Similarly, owls and pheasants are popular targets for hunters and trappers in some parts of the landscape (Sathyakumar et al. 2010; Inskipp et al. 2013).

    The majority of local people in the KL relies upon natural resources for meeting their essential requirements for fuel, livestock fodder, timber, and other basic materials (Chettri and Sharma 2006). The unsustainable, and often illegal, harvest of these resources is another major concern in the KL. Unsustainable harvesting of resources in the forests has caused thinning of woodlands, and affects vegetation structure and composition, which in turn influences occupancy and resource use patterns of birds (Chettri et al. 2005). Similarly, riverbed mining and the unsustainable extraction of sand, gravel and stones poses a serious threat to those bird species that breed in river areas (Acharya et al. 2010).

    Some invasive and alien species, including Water-hyacinth (Eichhornia crassipes), Bittervine (Mikania micrantha), Lantana (Lantana camara) and Crofton Weed (Ageratina adenophora) have invaded tropical and subtropical ecosystems in the landscape and pose serious threats to the bird diversity of the KL (Baral 2002; Dahal 2007).

    Unregulated tourism is another factor that poses immense pressure on local vegetation and birds of the Himalayan region, including the KL leading to increased fragmentation and deterioration of wildlife and their habitats (Chettri et al. 2001, 2002; Laiolo 2004).

    Global climate change also poses strong negative impacts on avifaunal populations of tropical mountains, including Himalayas, leading to bird species changing their nesting and migratory patterns, changing breeding seasonality and shifting their distribution range to obtain optimum food resources necessary for their survival (Ali 1962; Both et al. 2006; Acharya and Chettri 2012).

    The KL forms a part of the Eastern Himalaya which is identified as a part of the Himalayan biodiversity hotspot, one of 36 hotspots in the world (Conservation International 2017). The hotspot is home to the world's highest mountains including Mount Everest (highest) and Mount Kangchenjunga (third-highest), as well as important populations of numerous large birds and mammals including vultures, tigers, elephants, rhinos, and snow leopards. A rich variety of gene pools, species and ecosystems of global significance are found only in the region and most of them are under a high degree of threat (Mittermeier et al. 2004).

    Because of these multiple challenges to bird life and habitats in the KL, several conservation efforts have been devised and launched to protect vulnerable populations and environment. There are 19 protected areas in the KL of which nine are transboundary in nature (see Kandel et al. 2016 for details on the protected areas). These protected areas cover 30% of the total landscape area. All of these protected areas, except two, are located in KL-India—one in KL-Bhutan and one KL-Nepal. These protected areas provide habitat to many charismatic floral and faunal species, including more than 500 bird species (Chettri et al. 2008; Chaudhary et al. 2015).

    There is one Ramsar site—the Mai Pokhari Ramsar in the KL which is located in Ilam district in the eastern Nepal. Given its global significance as an important waterfowl habitat, it was declared as a Ramsar Site (No. 1850) during the 10th Conference of Parties to the Ramsar Convention (COP10) at Changwon, the Republic of Korea, on 28 October 2008. Located in Mai Pokhari VDC of Ilam district at an altitude of 2100 m, it has a catchment area of 12 hectares (WWF 2007). Mai Pokhari is a major habitat and breeding ground for more than 300 species of birds and some indigenous fauna such as the Tree Frog (Polypedates maculatus) and Himalayan Newt (Tylototriton verrucosus) (Chaudhary et al. 2015).

    A comparison of government policies of Bhutan, India and Nepal reveal that all three countries have supportive policies for bird conservation in place. Bhutan's national policy stipulates that 60% of the country maintain forests, many of which are large areas of pristine Himalayan forests and alpine habitats. These forests support threatened species such as Blyth's Tragopan and Chestnut-breasted Partridge. The forests on the lower slopes of the Bhutan are particularly important, as low-altitude forests have been extensively cleared in Nepal and parts of northeast India. This makes Bhutan a stronghold for birds such as Rufous-necked Hornbill.

    Similarly, the Government of India has an extensive body of constitutional provisions, laws and policies in place to protect biodiversity and their habitats. The Wildlife (Protection) Act 1972 (last amended in 2013) is an important statute that provides a powerful legal framework for protecting and managing wildlife habitats, and regulating and controlling trade in products derived from protected areas. In Nepal, the National Parks and Wildlife Conservation Act, 1973 (last amended in 1991) is the primary legislation that forms the basis for Nepal's biodiversity conservation programme. In Table 4, we provide a more comprehensive list and description of other government legislation and policies that support conservation of wildlife and their habitats in the KL.

    In this paper, we reviewed birds of the KL using 119 literature, and made a comprehensive documentation on species lists by taxonomy, threat status, distribution patterns at country levels, altitudinal zones and habitat preferences along with a list of IBAs. We found 618 bird species belonging to 19 orders, 77 families, and 41 species are identified as globally threatened species under IUCN red list status. We found the majority of bird species occupying the tropical zones and in forested areas.

    Despite the immense biological significance and continuous efforts of KL countries to conserve the rich biodiversity of the landscape, the region still faces numerous local, national, and transboundary challenges. Major constraints to long-term conservation in the region include habitat loss and fragmentation, hunting and trapping, unsustainable extraction of natural resources, invasive alien weeds, unregulated tourism, and global climate change. Protection and suitable management of IBAs could safeguard the survival of many threatened bird species in the landscape. Considering the cultural traditions for hunting and the low awareness level about wildlife conservation that prevail in the KL, conservation awareness programmes among students and community groups, as well as systematic and comprehensive bird surveys, particularly in the less explored areas of the KL that are identified as most intact and extensive habitat, are recommended. Long-term monitoring and assessment considering various drivers of change including climate change and their impacts on bird species could also fill existing knowledge gaps regarding Himalayan birds.

    Additional file 1. List of references.

    Additional file 2. Bird database.

    All authors contributed to developing the ideas and writing the manuscript. All authors have read and approved the final version of the manuscript.

    The authors would like to express their gratitude to Dr. David Molden, Director General of ICIMOD, for his inspiration and support. The authors would also like to thank Mr. Kabir Uddin, GIS and Remote Sensing Specialist, ICIMOD for providing the maps used in the article and Dr. Christopher Butler for English language editorial inputs. The views and interpretations in this publication are those of the authors and are not necessarily attributable to the affiliated organizations. The inputs provided by anonymous reviewers enabled us to bring this paper in its present form so we are really grateful.

    The authors declare that they have no competing interests.

    All data generated or analysed during this study are included in this article as supplementary information files.

    Not applicable.

    Not applicable.

  • Amato KR, Yeoman CJ, Kent A, Righini N, Carbonero F, Estrada A, Gaskins HR, Stumpf RM, Yildirim S, Torralba M. Habitat degradation impacts black howler monkey (Alouatta pigra) gastrointestinal microbiomes. ISME J. 2013;7:1344–53.
    Akaike H. Information theory and an extension of the maximum likelihood principle. In: Petrov BN, Csaki F, editors. Proceeding of the 2nd international symposium on information theory. Budapest: Akademiai Kiado; 1973. p. 267–81.
    Badano EI, Regidor HA, Núñez HA, Acosta R, Gianoli E. Species richness and structure of ant communities in a dynamic archipelago: effects of island area and age. J Biogeogr. 2005;32:221–7.
    Brown VK, Southwood TRE. Trophic diversity, niche breadth and generation times of exopterygote insects in a secondary succession. Oecologia. 1987;56:220–5.
    Burnham KP, Anderson DR. Model selection and multimodel inference: a practical information-theoretic approach. Berlin: Springer; 2002.
    Bush MB, Whittaker RJ. Krakatau: colonization patterns and hierarchies. J Biogeogr. 1991;18:341–56.
    Connel JH. Diversity in tropical rain forests and coral reefs—high diversity of trees and corals is maintained only in a non-equilibrium state. Science. 1978;199:1302–10.
    Connor EF, McCoy ED. The statistics and biology of the species–area relationship. Am Nat. 1979;113:791–833.
    Crowe TM. Lots of weeds: insular phytogeography of vacant urban lots. J Biogeogr. 1979;6:169–81.
    Durrett R, Levin S. Spatial models for species–area curves. J Theor Biol. 1996;179:119–27.
    Economo EP, Janda M, Guénard B, Sarnat E. Assembling a species–area curve through colonization, speciation and human-mediated introduction. J Biogeogr. 2016;44:1088–97.
    Feaga JS. Winter waterbird use and food resources of aquaculture lands in Mississippi. Mississippi State: Master of Science, Mississippi State University; 2014.
    Fox BJ, Fox MD. Factors determining mammal species richness on habitat islands and isolates: habitat diversity, disturbance, species interactions and guild assembly rules. Glob Ecol Biogeogr. 2000;9:19–37.
    Frey J, Bogan M, Yates T. Mountaintop island age determines species richness of boreal mammals in the American Southwest. Ecography. 2007;30:231–40.
    Graham MH. Confronting multicollinearity in ecological multiple regression. Ecology. 2003;84:2809–15.
    Hiddink JG, Jennings S, Kaiser MJ, Queirós AM, Duplisea DE, Piet GJ. Cumulative impacts of seabed trawl disturbance on benthic biomass, production, and species richness in different habitats. Can J Fish Aquat Sci. 2006;63:721–36.
    Horsák M, Hájek M, Spitale D, Hájková P, Dítě D, Nekola JC. The age of island-like habitats impacts habitat specialist species richness. Ecology. 2012;93:1106–14.
    Hosmer D, Lemeshow S. Applied logistic regression. 2nd ed. New York: Wiley; 2000.
    Hubbell SP. A unified theory of biogeography and relative species abundance and its application to tropical rain forests and coral reefs. Coral Reefs. 1997;16:S9–21.
    Krauss J, Alfert T, Steffan-Dewenter I. Habitat area but not habitat age determines wild bee richness in limestone quarries. J Appl Ecol. 2009;46:194–202.
    Kreft H, Jetz W, Mutke J, Kier G, Barthlott W. Global diversity of island floras from a macroecological perspective. Ecol Lett. 2008;11:116–27.
    Lantz SM, Gawlik DE, Cook MI. The effects of water depth and submerged aquatic vegetation on the selection of foraging habitat and foraging success of wading birds. Condor. 2010;112:460–9.
    Lomolino MV. The species–area relationship: new challenges for an old pattern. Prog Phys Geogr. 2001;25:1–21.
    Ma Z, Cai Y, Li B, Chen J. Managing wetland habitats for waterbirds: an international perspective. Wetlands. 2010;30:15–27.
    MacArthur RH, Wilson EO. An equilibrium theory of insular zoogeography. Evolution. 1963;17:373–87.
    MacArthur RH, Wilson EO. The theory of island biogeography. Princeton: Princeton University Press; 1967.
    Odum EP. The strategy of ecosystem development. Science. 1969;164:262.
    Palmer MW, White PS. Scale dependence and the species–area relationship. Am Nat. 1994;144:717–40.
    Power DM. Numbers of bird species on the California islands. Evolution. 1972;26:451–63.
    Rejmánek M, Rejmánková E. Biogeography of artificial islands: effects of age, area, elevation, and isolation on plant species richness. Preslia. 2002;74:307–14.
    Rosenzweig ML. Species diversity in space and time. Cambridge: Cambridge University Press; 1995.
    Ross KA, Fox BJ, Fox MD. Changes to plant species richness in forest fragments: fragment age, disturbance and fire history may be as important as area. J Biogeogr. 2002;29:749–65.
    Rybicki J, Hanski I. Species–area relationships and extinctions caused by habitat loss and fragmentation. Ecol Lett. 2013;16:27–38.
    Scheffer M, Van Geest G, Zimmer K, Jeppesen E, Søndergaard M, Butler M, Hanson M, Declerck S, De Meester L. Small habitat size and isolation can promote species richness: second-order effects on biodiversity in shallow lakes and ponds. Oikos. 2006;112:227–31.
    Scheiner SM. Six types of species–area curves. Glob Ecol Biogeogr. 2003;12:441–7.
    Simberloff D. Species turnover and equilibrium island biogeography. Science. 1976;194:572.
    Sousa WP. The role of disturbance in natural communities. Annu Rev Ecol Syst. 1984;15:353–91.
    Storch D, Izling AL, Gaston KJ. Geometry of the species–area relationship in central European birds: testing the mechanism. J Anim Ecol. 2003;72:509–19.
    Storch D, Keil P, Jetz W. Universal species–area and endemics–area relationships at continental scales. Nature. 2012;488:78–81.
    Tittensor DP, Micheli F, Nyström M, Worm B. Human impacts on the specie-area relationship in reef fish assemblages. Ecol Lett. 2007;10:760–72.
    Tischendorf L, Fahrig L. On the usage and measurement of landscape connectivity. Oikos. 2000;90:7–19.
    Tischendorf L, Fahrig L. On the use of connectivity measures in spatial ecology. A reply. Oikos. 2001;95:152–5.
    Valente LM, Etienne RS, Phillimore AB. The effects of island ontogeny on species diversity and phylogeny. Proc Biol Sci. 2014;281:20133227.
    Vera CF, Rocha CF. Habitat disturbance and small mammal richness and diversity in an Atlantic rainforest area in southeastern Brazil. Brazil J Biol. 2006;66:983–90.
    Wagner CE, Harmon LJ, Seehausen O. Cichlid species–area relationships are shaped by adaptive radiations that scale with area. Ecol Lett. 2014;17:583–92.
    Wan WJ, Zhou LZ, Ping L. Impact of coal mining subsidence on species composition and diversity of avian community. Sichuan J Zool. 2015;34:773–9 (in Chinese).
    Williamson M. Relationship of species number to area, distance and other variables. Dordrecht: Springer; 1988.
    Yuan Y, Zeng G, Liang J, Li X, Li Z, Zhang C, Huang L, Lai X, Lu L, Wu H. Effects of landscape structure, habitat and human disturbance on birds: a case study in East Dongting Lake wetland. Ecol Eng. 2014;67:67–75.
  • Related Articles

  • Cited by

    Periodical cited type(9)

    1. Vivek Chetry, Prasanta Kumar Saikia, Malabika Kakati Saikia, et al. Influence of heterogeneous habitats on the taxonomic and functional diversity of avifauna in an eastern Himalayan foothill landscape, India. Trees, Forests and People, 2024. DOI:10.1016/j.tfp.2024.100764
    2. Binod Bhattarai, Dipendra Adhikari, Jagan Nath Adhikari, et al. Effects of invasive alien plants and habitat structure on bird assemblages in a unique lowland forest in eastern Nepal. Ornis Hungarica, 2024, 32(2): 1. DOI:10.2478/orhu-2024-0019
    3. Jyoti Tirkey, K. R. Sahu, Pratibha Pandey. SEASONAL VARIATION AND ABUNDANCE, RESIDENTIAL AND IUCN STATUS OF AVIAN DIVERSITY IN FOREST COMMUNITY IN JASHPUR DISTRICT (C.G.). ShodhKosh: Journal of Visual and Performing Arts, 2024, 5(6) DOI:10.29121/shodhkosh.v5.i6.2024.2760
    4. Kiran Sharma, Anup Saikia, Pankaj Thapa, et al. Aboveground biomass and carbon stock assessment in the Eastern Himalaya foothills along the Indo-Bhutan border. Australian Geographer, 2022, 53(3): 241. DOI:10.1080/00049182.2022.2092992
    5. Kamal Joshi, Deepak Kumar. Avian species composition and distribution along elevational zone in forest habitat of Nainital district (Western Himalaya) of Uttarakhand, India. Trees, Forests and People, 2022, 7: 100177. DOI:10.1016/j.tfp.2021.100177
    6. Lam Norbu, Phuntsho Thinley, Tandin Wangchuck, et al. On the high bird diversity in the non-protected regions of Trashiyangtse District in Bhutan. Journal of Threatened Taxa, 2021, 13(9): 19274. DOI:10.11609/jott.6843.13.9.19274-19292
    7. Alexander R. O’Neill, Prem K. Chhetri, Bijoy Chhetri, et al. Establishing ecological baselines around a temperate Himalayan peatland. Wetlands Ecology and Management, 2020, 28(2): 375. DOI:10.1007/s11273-020-09710-7
    8. Janita Gurung, Nakul Chettri, Eklabya Sharma, et al. Evolution of a transboundary landscape approach in the Hindu Kush Himalaya: Key learnings from the Kangchenjunga Landscape. Global Ecology and Conservation, 2019, 17: e00599. DOI:10.1016/j.gecco.2019.e00599
    9. Nakul Chettri, Srijana Joshi, Bandana Shakya, et al. Mountain Landscapes in Transition. Sustainable Development Goals Series, DOI:10.1007/978-3-030-70238-0_31

    Other cited types(0)

Catalog

    Figures(4)  /  Tables(2)

    Article Metrics

    Article views (252) PDF downloads (8) Cited by(9)

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return