A checklist of the winter bird community in different habitat types of Rosekandy Tea Estate of Assam, India

 

Aftab Ahmed 1 & Mithra Dey 2

 

1,2 Department of Ecology and Environmental Science, Assam University, Silchar, Assam 788011, India

1 aftabahmed372002@yahoo.co.in, 2 mithradey@gmail.com (corresponding author)

 

 

 

Abstract: This study was aimed at preparing an inventory of the avifauna and to document the species composition of birds during winter in different habitat types of RosekandyTea Estate of Cachar District of Assam.  Four habitat types, viz., tea plantation, ecotone zone, secondary growth forest and water bodies were selected within the tea estate and surveyed from mid-December 2010 (early winter) to mid-April 2011 (late winter) covering four months of survey.  A total of 88 species were recorded during the survey period with the highest number of species in ecotone zone (n=63), followed by secondary forest (n=60), tea plantation (n=48) and water bodies (n=17).  The species were further categorized into different feeding and habitat guilds to study the distribution of bird species in different habitat types according to various guilds.

 

Keyword: Avifauna, ecotone, habitat, secondary growth forest, tea plantation.

 

 

 

doi: http://dx.doi.org/10.11609/JoTT.o3246.5478-84  | ZooBank:urn:lsid:zoobank.org:pub:97FA1B39-32BD-4F6C-9329-FDB3DD4D962C

 

Editor: Rajiv Kalsi, M.L.N. College, Yamuna Nagar, Haryana, India.          Date of publication: 26 February 2014 (online & print)

 

Manuscript details: Ms # o3246 | Received 04 July 2012 | Final received 12 February 2014 | Finally accepted 13 February 2014

 

Citation: Ahmed, A. & M. Dey (2014).A checklist of the winter bird community in different habitat types of RosekandyTea Estate of Assam, India. Journal of Threatened Taxa6(2): 5478–5484; http://dx.doi.org/10.11609/JoTT.o3246.5478-84

 

Copyright: © Ahmed & Dey 2014. Creative Commons Attribution 3.0 UnportedLicense. JoTT allows unrestricted use of this article in any medium, reproduction and distribution by providing adequate credit to the authors and the source of publication.

 

Funding: None.

 

Competing Interest: The authors declare no competing interests.

 

Acknowledgements: Authors are thankful to the authorities and staffs of Rosekandy Tea Estate, Cachar, Assam for their co-operation and help during the study. The authors are grateful to the Department of Ecology and Environmental Science, AUS. We also sincerely express our thanks to the Subject Editor and anonymous referees for their valuable comments on the manuscript.

 

 

 

For image, table -- click here

 

 

Habitat destruction in the tropics in the late 20th century was characterized by high rates of conversion of natural landscapes to agricultural landscapes (Stotz et al. 1996).  Often overlooked, however, is the fact that the conversion of tropical forests for agricultural use is rarely complete, and often not permanent. Within the agricultural landscape, one can find a significant amount of forested area in the form of managed multistoreyagroforestry systems, or agroecosystems, whose features of structural complexity, microclimate buffering, and diversity of canopy food plants retain high biodiversity and contribute to the protection of forest biota (Beer 1987; Alcorn 1990; Perfecto et al. 1996).

In the past decade, a growing number of studies have focused on biodiversity in shaded agroforestry systems using birds as indicators of biodiversity (Parrish & Petit 1996; Wunderle& Latta 1996; Greenberg et al. 1997).  Bird species diversity in shaded plantations is nearly always reported to be considerably higher than in other types of monoculture cultivation (Wunderle & Latta 1996; Petit et al. 1999; Tejeda-Cruz & Sutherland 2004).  Most pieces of research found shaded plantations to support only a few particular guilds of the bird population.  Generally, more omnivorous, frugivorous and nectivorous, but fewer insectivorous species occupy plantations than natural forests (Canaday 1996; Shahabuddin 1997; Petit et al. 1999); generalist and open-grassland species are abundant in plantations than forest species (Hughes et al. 2002; Naidoo2004).

As for tea plantations, very little research has been conducted regarding biodiversity assemblage in the tea gardens.  Shaded tea plantations strictly follow monoculture cultivation of the tea plant supported by very few species of deciduous shade trees.  The sensitivity of tea plants to water, shade and pest also further complicate the functioning of the tea gardens and are thus to a large extent dependent on human intervention.  However, tea plantations accompanied by neighboring patches of forest and water bodies greatly contribute in maintaining a high diversity of animal species in the tea gardens. The variety of forest areas, water bodies and other vegetation cover along with the tea plantation thus forms the actual driving factor for biodiversity of the tea estates. The ‘hard’ edges of tea plantation, which are formed by abrupt changes from tea shrubs to other vegetation cover such as forest or agricultural crop may also effect the movement and distribution of wildlife.

NortheasternIndia supports some of the rarest, least known and most sought-after birds of the oriental region.  The numerous tea estates in northeastern India thus provide a potential habitat to the diverse bird community of the region. Barak Valley in Assam, which has very few pristine forestland but a large number of tea estates has an opportunity to sustain its avifaunal diversity within these tea plantations. A proper management of shade trees, forest patches and water reservoirs in the tea estates, keeping in view the needs of the bird community as well as human needs can form an effective strategy to secure the avian diversity of the region.

 

Material and Methods

Study site: The Rosekandy Tea Estate is situated at Barjalenga in Cachar District of Assam.  It is geographically located within 24042’29”–24041’31”N and 92041’52”–92042’39”E (Image 1).  The maximum temperature in the study area ranged from 23–34.4 0C; minimum temperature from 11.4–26 0C; and relative humidity from 60.4–96 %.  The total area under the tea estate is about 1702.01ha out of which, 562.80ha is used at present for tea plantation while the remaining 1309.78ha consists of uncultivated lands, secondary forest growth and water reservoirs.  The different vegetation types and plantation patterns result in the formation of various microhabitats in the tea gardens where different species of birds reside according to their habitat preferences.  Therefore, the study area was classified according to their physiognomic and floristic composition into four different habitat types:

Tea Plantation (TP): The plantation areas contains tea shrubs (Camelliasinensis) that reaches a height of 0.5–1 m with uniformly interspaced shade trees which generally consists of species of Albizzia odoratissima, Albizzia lebbec, Deris robusta, Dalbergia sisu, Albizzia chinensis etc.  This habitat type has an open canopy and two storied vegetation structures.

Secondary Growth Forest (SF): The areas that are not cultivated are covered with secondary semi ever-green forest and marsh lands.  The prominent species consists of Dysoxylum sp., Saprosma ternatum, Vitex sp.,Vatica lancaefolia, Castanopsis sp., Mesua floribuanda, Pterygota alata, Vatica lancaefolia,Glochidion sp., Knema linifolia, Ficus sp.,Artocarpus chama, Cynometra polyandra, Mangifera indica, Bombax ceiba, Xerospermum glabratum, Macaranga peltata, Litsea monopetala etc. Bamboo patches and reed growth near the edges of the forest are also common.

Ecotone Zone (EZ): The third habitat type is the ecotone zone between the secondary forest and tea plantation.  This zone is formed at the areas where the tea plantation abruptly ends and the forest cover begins.  Contrasting to conventionalecotone, this area does not show a gradient in floral community but displays an abrupt switch from one habitat type to another.

Water Body (WB): The tea estate contains many large water reservoirs and ponds which store water during the rainy seasons.  This stored water is used during the dry season to irrigate the tea gardens.  These water bodies form an ideal habitat for aquatic fauna and aquatic birds and hence are selected as the fourth type of habitat.  Along with this, the natural streams and tea gardens irrigation canals also form other sources of water bodies.

 

Methods

The sampling was carried out during the winter months starting from mid-December 2010 (early winter) to mid-April 2011 (late winter) covering four months of survey.  Birds were sampled using the line transects method (Buckland et al. 1993) and identification was done using standard field guides (Grimmettet al. 2001; Ali 2002).  Three fixed transects of 700m in each habitat type were surveyed every 15 days during the morning hours between 0600–1000 hr. The opportunistic counts during other times of the day are also included in the checklist.  We followed the nomenclature and taxonomic sequence of Manakadan& Pittie (2001).  To explore species composition in terms of the feeding guilds and habitat guilds, bird species are classified accordingly to various feeding and habitat categories based on observations and scientific literature (Grimmett et al. 2001; Ali 2002).

 

Results

A total of 88 species belonging to 38 families (Table 1) were recorded in the Rosekandy Tea Estate during the four-month survey.  The highest number of species were recorded in the ecotonezone (n=63), followed by secondary forest (n=60), tea plantation (n=48) and water bodies (n=17).  According to the various feeding guilds, out of the 88 species, the highest number of species were omnivores (n=32), followed by insectivores (n=26), phytophage (n=16), piscivores (n=9) and carnivores (n=5).  Habitat wise, most of the species were generalist (n=30) and forest inhabitants (n=24).  Aquatic (n=17) and openlandinhabitants (n=17) form the rest of the surveyed population.

 

Discussion

The Rosekandy tea estate consists of different habitat types which are capable of sustaining a diverse population of avifauna.  The study demonstrated a rich diversity by the presence of a total of 88 species within the different habitat types of the tea estate.  A similar study by Deb & Gupta (2010) recorded a total of 76 species in four different landscape types of Cachar District.

The study presented signifies the potential of tea agroforestry systems along with their adjoining forest patches in conserving the bird population of the region.  The study shows similar trends of species richness as studied in other tea plantations (Githiru et al. 2009) and different agroforestry systems (Greenberg et al. 1997; Tejeda-Cruz & Sutherland 2004) around the world.  This study recorded similar species of birds from the tea plantation as has been observed in other bird surveys in this area (Deb & Gupta 2010; Devet al. 2010).

The variation in species richness in different habitat types within the tea estate contrasted with results from previous studies.  In this study, species richness was higher in secondary forest growth as compared to tea plantation while earlier studies (Deb & Gupta 2010) reported higher species richness in tea plantations than the adjutant secondary forest. However, the results coincide with studies in most of the coffee plantation where neighboring forest patches contained more species than plantation areas (Wunderle & Latta 1996; Greenberg et al. 1997; Petit et al. 1999).  The ecotonezone with the highest species richness denoted an edge effect of this zone.

Feeding guilds in all four habitats were largely composed of insectivore and omnivore species with a small number of phytophagous, carnivore and piscivore species.  Similar studies in coffee (Greenberg et al. 1997; Tejeda-Cruz & Sutherland 2004) and cocoa (Reitsma et al. 2001; Harvey et al. 2007) plantations showed a higher abundance of omnivore species than insectivore species.  However, studies in other tea plantations revealed a higher proportion of insectivore and less omnivore guilds as they were able to adapt to different habitat types and food resources (Githiru et al. 2009).

The habitat guild in the studied site showed a similar pattern with the studies in other agroforestry systems (Greenberg et al. 1997; Reitsma et al. 2001; Tejeda-Cruz & Sutherland 2004) which recorded the higher number of generalist species.  Open-habitat species are more abundant in tea plantation coinciding with studies in cocoa and banana plantation (Harvey et al. 2007).

Further studies and monitoring of bird populations in different tea estates can reveal a more complete description of patterns of bird assemblage and species composition in the tea agroforestry systems and hence contribute to the conservation effort for birds in tea gardens.

           

References

 

Alcorn, J. (1990). Indigenous agroforestry systems in the Latin American tropic, Agroecologyand Small Farm Development. CRC Press, Boca Raton, Fl., 203–218pp.

Ali, S. (2002). The Book of Indian Bird - 13th Edition. Oxford University Press, 345pp.   

Beer, J. (1987). Advantages, disadvantages and desirable characteristics of shade trees for coffee, cacao and tea. Agroforestry Systems 5: 3–13.

Buckland, S.T., D.R Anderson, K.P. Burnham, J.L. Laake, D.L. Borchers & L. Thomas (1993). Introduction to Distance Sampling-Estimating Abundance of Biological Population. Oxford University Press. 104–140pp

Canaday, C. (1996). Loss of insectivorous birds along a gradient of human impact in Amazonia. Biological Conservation 136: 212–231.

Deb, N. & A. Gupta (2010). Avian community analysis in fragmented landscapes of CacharDistrict, Assam. Assam University Journal of Science & Technology, Biological and Environmental Sciences5(1): 75–84.

Dev, B., A. Gupta & P.C. Bhattarcharjee (2010). Avifaunal Composition and diversity in Barak Valley, Assam. National Seminar on Biodiversity Conservation, Assam University, Silchar, Assam 102–112pp.

Githiru, M., S. Karimi& T. Imboma (2009). Unilever Kenya Ltd. (Kericho): Avifaunal Assessment Report. Unilever Tea Kenya Ltd., Nairobi 15–27pp

Greenberg, R., P. Bichier & J. Sterling (1997). Bird populations in rustic and planted shade coffee plantations of eastern Chiapas, Mexico. Biotropica 29(4): 501–514.

Grimmett, R., C Inskipp & T. Inskipp(2001). Pocket Guide to The Birds of The Indian Subcontinent. Oxford University Press, 338pp.

Harvey, C.A. & J.A.G Villalobos (2007).Agroforestry systems conserve species-rich but modified assemblages of tropical birds and bats. Biodiversity Conservation 16: 2257–2292.

Hughes, J.B., G.C. Daily & P.R. Ehrlich (2002). Conservation of tropical forest birds in countryside habitats. Ecological Letters 5: 121–129.

Manakadan, R. & A. Pittie(2001). Standardized common and scientific names of the birds of the Indian subcontinent. Buceros 6(1): 1–37.

Naidoo, R. (2004). Species richness and community composition of songbirds in tropical forest-agricultural landscape. Animal Conservation 7: 93–105.

Parrish, J.D. & L.J. Petit (1996). Value of shade coffee plantation for tropical birds: landscape and vegetation effects. Proceedings of Environmental Enhancement through Agriculture Conference, Boston, MA.Tufts University 113–121pp.

Perfecto, I., R.A. Rice, R. Greenberg & M.E. van der Voort (1996). shadecoffee: a disappearing refuge for biodiversity; shade coffee plantations can contain as much biodiversity as forest habitats. Bioscience46: 598–608.

Petit, L.J., D.R. Petit, D.G. Christian & H.D.W. Powell (1999). Bird communities of natural and modified habitats in Panama. Ecography 22: 292–304.

Reitsma, R., J.D. Parrish & W. McLarney (2001). The role of cacao plantations in maintaining forest avian diversity in southeastern Costa Rica. Agroforestry System 53(2): 185–193.

Shahabuddin, G. (1997). Preliminary observations on the role of coffee plantations as avifaunal refuges in the Palni Hills of the Western Ghats. Journal of the Bombay Natural History Society94: 10–21.

Stotz, D.F., J.W. Fitzpatrick, T.A. Parker & D.K. Moskovitz(1996). Neotropical birds - Ecology and conservation. University of Chicago Press, Chicago, 520pp.

Tejeda-Cruz, C. & W.J. Sutherland (2004). Bird responses to shade coffee production. Animal Conservation 7: 169–179.

Wunderle, J.M. Jr. & S.C. Latta(1996). Avian abundance in sun and shade coffee plantations and remnant pine forest in the Cordillera Central, Dominican Republic. Ornitologia Neotropical 7: 19–34.