Tringa nebularia 


Taxonomy [top]

Kingdom Phylum Class Order Family
Animalia Chordata Aves Charadriiformes Scolopacidae

Scientific Name: Tringa nebularia
Species Authority: (Gunnerus, 1767)
Regional Assessments:
Common Name(s):
English Common Greenshank, Greenshank
French Chevalier aboyeur
Taxonomic Source(s): del Hoyo, J., Collar, N.J., Christie, D.A., Elliott, A. and Fishpool, L.D.C. 2014. HBW and BirdLife International Illustrated Checklist of the Birds of the World. Lynx Edicions BirdLife International.

Assessment Information [top]

Red List Category & Criteria: Least Concern ver 3.1
Year Published: 2015
Date Assessed: 2012-05-03
Assessor(s): BirdLife International
Reviewer(s): Butchart, S.
Facilitator/Compiler(s): Ekstrom, J., Butchart, S., Malpas, L. & Symes, A.
This species has an extremely large range, and hence does not approach the thresholds for Vulnerable under the range size criterion (extent of occurrence <20,000 km2 combined with a declining or fluctuating range size, habitat extent/quality, or population size and a small number of locations or severe fragmentation). The population trend appears to be stable, and hence the species does not approach the thresholds for Vulnerable under the population trend criterion (>30% decline over ten years or three generations). The population size is very large, and hence does not approach the thresholds for Vulnerable under the population size criterion (<10,000 mature individuals with a continuing decline estimated to be >10% in ten years or three generations, or with a specified population structure). For these reasons the species is evaluated as Least Concern.
Previously published Red List assessments:
2012 Least Concern (LC)
2009 Least Concern (LC)
2008 Least Concern (LC)
2004 Least Concern (LC)
2000 Lower Risk/least concern (LR/lc)
1994 Lower Risk/least concern (LR/lc)
1988 Lower Risk/least concern (LR/lc)

Geographic Range [top]

Range Description: There is evidence to suggest that the European population (200,000-510,000 pairs, occupying 50-74% of the global breeding range) has declined by up to 30% over ten years (three generations), but this may reflect shifts in breeding populations, populations in Asia are not thought to be declining and wintering populations in Africa appear to be increasing.

Countries occurrence:
Afghanistan; Albania; Algeria; Angola (Angola); Armenia (Armenia); Australia; Austria; Azerbaijan; Bahrain; Bangladesh; Belarus; Belgium; Benin; Bhutan; Bosnia and Herzegovina; Botswana; British Indian Ocean Territory; Brunei Darussalam; Bulgaria; Burkina Faso; Burundi; Cambodia; Cameroon; Cape Verde; Central African Republic; Chad; China; Christmas Island; Cocos (Keeling) Islands; Comoros; Congo; Congo, The Democratic Republic of the; Côte d'Ivoire; Croatia; Cyprus; Czech Republic; Denmark; Djibouti; Egypt; Equatorial Guinea; Eritrea; Estonia; Ethiopia; Finland; France; Gabon; Gambia; Georgia; Germany; Ghana; Greece; Guam; Guinea; Guinea-Bissau; Hong Kong; Hungary; India; Indonesia; Iran, Islamic Republic of; Iraq; Ireland; Israel; Italy; Japan; Jordan; Kazakhstan; Kenya; Korea, Democratic People's Republic of; Korea, Republic of; Kuwait; Kyrgyzstan; Lao People's Democratic Republic; Latvia; Lebanon; Lesotho; Liberia; Libya; Liechtenstein; Luxembourg; Macedonia, the former Yugoslav Republic of; Madagascar; Malawi; Malaysia; Maldives; Mali; Malta; Mauritania; Mauritius; Mayotte; Micronesia, Federated States of ; Moldova; Mongolia; Montenegro; Morocco; Mozambique; Myanmar; Namibia; Nepal; Netherlands; New Zealand; Niger; Nigeria; Northern Mariana Islands; Norway; Oman; Pakistan; Palau; Palestinian Territory, Occupied; Papua New Guinea; Philippines; Poland; Portugal; Qatar; Réunion; Romania; Russian Federation; Rwanda; Sao Tomé and Principe; Saudi Arabia; Senegal; Serbia (Serbia); Seychelles; Sierra Leone; Singapore; Slovakia; Slovenia; Solomon Islands; Somalia; South Africa; South Sudan; Spain; Sri Lanka; Sudan; Swaziland; Sweden; Switzerland; Syrian Arab Republic; Taiwan, Province of China; Tajikistan; Tanzania, United Republic of; Thailand; Timor-Leste; Togo; Tunisia; Turkey; Turkmenistan; Uganda; Ukraine; United Arab Emirates; United Kingdom; Uzbekistan; Viet Nam; Western Sahara; Yemen; Zambia; Zimbabwe
Barbados; Bermuda; Canada; Faroe Islands; French Southern Territories; Iceland; New Caledonia; Puerto Rico; United States (Georgia - Native)
Continuing decline in area of occupancy (AOO): Unknown
Extreme fluctuations in area of occupancy (AOO): No
Estimated extent of occurrence (EOO) - km2: 12100000
Continuing decline in extent of occurrence (EOO): Unknown
Extreme fluctuations in extent of occurrence (EOO): No
Continuing decline in number of locations: Unknown
Extreme fluctuations in the number of locations: No
Range Map: Click here to open the map viewer and explore range.

Population [top]

Population: The global population is estimated to number c.440,000-1,500,000 individuals (Wetlands International, 2006), while national population estimates include: < c.10,000 individuals on migration and c.1,000-10,000 wintering individuals in China; c.1,000-10,000 individuals on migration and c.1,000-10,000 wintering individuals in Taiwan; c.1,000-10,000 individuals on migration and < c.50 wintering individuals in Korea; c.1,000-10,000 individuals on migration and c.1,000-10,000 wintering individuals in Japan and c.10,000-100,000 breeding pairs and c.1,000-10,000 individuals on migration in Russia (Brazil 2009).

Trend Justification:  The overall population trend is stable, although some populations have unknown trends (Wetlands International 2006).
Current Population Trend: Stable
Additional data:
Continuing decline of mature individuals: Unknown
Extreme fluctuations: No Population severely fragmented: No
Continuing decline in subpopulations: Unknown
Extreme fluctuations in subpopulations: No All individuals in one subpopulation: No

Habitat and Ecology [top]

Habitat and Ecology: Behaviour This species is fully migratory and generally migrates overland on a broad front, although the majority of Western European birds passes through coastal and estuarine sites (del Hoyo et al. 1996, Snow and Perrins 1998). The Wadden Sea for example is used by many Fennoscandian birds as a stop-over and moulting site from late-April to mid-May (del Hoyo et al. 1996). Most palearctic birds are trans-Saharan migrants (del Hoyo et al. 1996), the main autumn passage through northern and temperate Europe occurring from the second week of July to late-October (Snow and Perrins 1998). One parent (usually the female) leaves the breeding territory first from late-June to early July (del Hoyo et al. 1996, Snow and Perrins 1998), with the other parent and juveniles following around 3-6 weeks later (Snow and Perrins 1998). Flocks arrive in southern Africa and Australia from August to September, and depart again in March for the northward return migration (del Hoyo et al. 1996). The species departs for its breeding grounds during the evening (Hockey et al. 2005) and once there it breeds between late-April and June (del Hoyo et al. 1996). Some non-breeding birds may also remain in the south throughout the summer (del Hoyo et al. 1996, Snow and Perrins 1998). The species normally breeds in very dispersed pairs (Johnsgard 1981), but on passage it can occur singly or in small flocks (flocks of 20-25 are common in southern Africa) (Snow and Perrins 1998), although congregations of 100 or more may very rarely occur at high tide or at roosting sites (Urban et al. 1986). This species feeds both diurnally and nocturnally (del Hoyo et al. 1996). Habitat Breeding This species breeds in the boreal forest zone from sea level to 1,200 m in Norway (Johnsgard 1981, Snow and Perrins 1998)(although predominantly up to 450 m) (Snow and Perrins 1998), in swampy forest clearings, woody moorland, open bogs and marshes (including raised and blanket bogs) (del Hoyo et al. 1996), and eutrophic lakes with margins of dead and decaying vegetation (Johnsgard 1981). It avoids bare or broken barren expanses, mountain escarpments, and closed forests with very dense, tall vegetation (Snow and Perrins 1998). Non-breeding In its wintering grounds this species frequents a variety of freshwater, marine and artificial wetlands, including swamps, open muddy or rocky shores of lakes and large rivers, sewage farms, saltworks, inundated rice-fields (del Hoyo et al. 1996), ponds, reservoirs (Snow and Perrins 1998), flooded grasslands (Hockey et al. 2005), saltmarshes, sandy or muddy coastal flats, mangroves, estuaries (del Hoyo et al. 1996), lagoonsand pools on tidal reefs (Snow and Perrins 1998) or exposed coral (Urban et al. 1986), although it generally avoids open coastline (del Hoyo et al. 1996). On migration this species occurs on inland flooded meadows, dried-up lakes, sandbars and marshes (del Hoyo et al. 1996). Diet This species is chiefly carnivorous, its diet consisting of insects and their larvae (especially beetles), crustaceans, annelids, molluscs, amphibians (del Hoyo et al. 1996), small fish (mullet Liza spp., clinids Clinus spp. and tilapia Oreochromis spp.) (Hockey et al. 2005) and occasionally rodents (del Hoyo et al. 1996). Breeding site The nest is a shallow scrape on open ground, often in clearings in woods (Snow and Perrins 1998), and is typically placed next to a piece of dead wood (del Hoyo et al. 1996), or beside rocks, trees (Johnsgard 1981), fences and sticks (for use as nest markers) (Snow and Perrins 1998).
Systems: Terrestrial; Freshwater; Marine
Continuing decline in area, extent and/or quality of habitat: Unknown
Generation Length (years): 6.3
Movement patterns: Full Migrant
Congregatory: Congregatory (and dispersive)

Threats [top]

Major Threat(s): In the Chinese, North Korean and South Korean regions of the Yellow Sea this species is threatened by the degradation and loss of its preferred wetland habitats through environmental pollution, reduced river flows and human disturbance (Kelin and Qiang 2006).

Citation: BirdLife International. 2015. Tringa nebularia. The IUCN Red List of Threatened Species 2015: e.T22693220A67222512. . Downloaded on 25 November 2015.
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