|Scientific Name:||Numenius phaeopus|
|Species Authority:||(Linnaeus, 1758)|
|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.|
|Red List Category & Criteria:||Least Concern ver 3.1|
|Reviewer(s):||Butchart, S. & Symes, A.|
|Facilitator/Compiler(s):||Butchart, S., Malpas, L., Ekstrom, J.|
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). Despite the fact that the population trend appears to be decreasing, the decline is not believed to be sufficiently rapid to approach the thresholds for Vulnerable under the population trend criterion (>30% decline over ten years or three generations). The population size is extremely 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:||
Native:Albania; Algeria; American Samoa (American Samoa); Angola (Angola); Anguilla; Antigua and Barbuda; Argentina; Armenia (Armenia); Aruba; Australia; Austria; Azerbaijan; Bahamas; Bahrain; Bangladesh; Barbados; Belarus; Belgium; Belize; Benin; Bermuda; Bhutan; Bolivia, Plurinational States of; Bonaire, Sint Eustatius and Saba; Bosnia and Herzegovina; Botswana; Brazil; British Indian Ocean Territory; Brunei Darussalam; Bulgaria; Burundi; Cambodia; Cameroon; Canada; Cape Verde; Cayman Islands; Chile; China; Christmas Island; Cocos (Keeling) Islands; Colombia; Comoros; Congo; Congo, The Democratic Republic of the; Costa Rica; Côte d'Ivoire; Croatia; Cuba; Curaçao; Cyprus; Czech Republic; Denmark; Djibouti; Dominica; Dominican Republic; Ecuador; Egypt; El Salvador; Equatorial Guinea; Eritrea; Estonia; Ethiopia; Falkland Islands (Malvinas); Faroe Islands; Fiji; Finland; France; French Guiana; Gabon; Gambia; Georgia; Germany; Ghana; Gibraltar; Greece; Greenland; Guadeloupe; Guam; Guatemala; Guinea; Guinea-Bissau; Guyana; Haiti; Honduras; Hong Kong; Hungary; Iceland; India; Indonesia; Iran, Islamic Republic of; Iraq; Israel; Italy; Jamaica; Japan; Kazakhstan; Kenya; Kiribati; Korea, Democratic People's Republic of; Korea, Republic of; Kuwait; Kyrgyzstan; Latvia; Lebanon; Liberia; Libya; Luxembourg; Macao; Macedonia, the former Yugoslav Republic of; Madagascar; Malawi; Malaysia; Maldives; Mali; Malta; Marshall Islands; Martinique; Mauritania; Mauritius; Mayotte; Mexico; Micronesia, Federated States of ; Moldova; Mongolia; Montenegro; Montserrat; Morocco; Mozambique; Myanmar; Namibia; Nauru; Nepal; Netherlands; New Caledonia; New Zealand; Nicaragua; Nigeria; Norfolk Island; Northern Mariana Islands; Norway; Oman; Pakistan; Palau; Palestinian Territory, Occupied; Panama; Papua New Guinea; Peru; Philippines; Poland; Portugal; Puerto Rico; Qatar; Réunion; Romania; Russian Federation; Rwanda; Saint Kitts and Nevis; Saint Lucia; Saint Pierre and Miquelon; Saint Vincent and the Grenadines; Samoa; Sao Tomé and Principe; Saudi Arabia; Senegal; Serbia (Serbia); Seychelles; Sierra Leone; Singapore; Slovakia; Solomon Islands; Somalia; South Africa; South Georgia and the South Sandwich Islands; Spain; Sri Lanka; Sudan; Suriname; Svalbard and Jan Mayen; Sweden; Switzerland; Syrian Arab Republic; Taiwan, Province of China; Tanzania, United Republic of; Thailand; Timor-Leste; Togo; Trinidad and Tobago; Tunisia; Turkey; Turkmenistan; Turks and Caicos Islands; Tuvalu; Uganda; Ukraine; United Arab Emirates; United Kingdom; United States (Georgia); Uruguay; Uzbekistan; Vanuatu; Venezuela, Bolivarian Republic of; Viet Nam; Western Sahara; Yemen; Zambia; Zimbabwe
Vagrant:Afghanistan; Burkina Faso; French Southern Territories; Grenada; Jordan; Liechtenstein; Slovenia; Tajikistan; Virgin Islands, British; Virgin Islands, U.S.
|Continuing decline in area of occupancy (AOO):||Unknown|
|Extreme fluctuations in area of occupancy (AOO):||No|
|Estimated extent of occurrence (EOO) - km2:||4790000|
|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:||The global population is estimated to number c.1,000,000-2,300,000 individuals (Wetlands International 2006), while national population estimates include: c.1,000-10,000 individuals on migration and c.50-1,000 wintering individuals in China; c.1,000-10,000 individuals on migration and c.50-1,000 wintering individuals in Taiwan; c.1,000-10,000 individuals on migration and c.50-1,000 wintering individuals in Japan and c.10,000-100,000 breeding pairs and > c.10,000 individuals on migration in Russia (Brazil 2009).
Trend Justification: The overall population trend is decreasing, although some populations may be stable and others have unknown trends (Wetlands International 2006). This species has undergone a large and statistically significant decrease over the last 40 years in North America (-84.7% decline over 40 years, equating to a -37.5% decline per decade; data from Breeding Bird Survey and/or Christmas Bird Count: Butcher and Niven 2007) Note, however, that these surveys cover less than 50% of the species's range in North America.
|Current Population Trend:||Decreasing|
|Habitat and Ecology:||Behaviour This species is fully migratory and travels over land on a broad front utilising few staging areas on route (in autumn no known concentrated staging occurs) (del Hoyo et al. 1996, Snow and Perrins 1998). It breeds from May to August (Hayman et al. 1986) either in well-dispersed (Johnsgard 1981) solitary pairs (del Hoyo et al. 1996) or in loose groups depending on the topography of the land (Snow and Perrins 1998). The autumn migration occurs from July onwards (Hayman et al. 1986) with the return passage to the breeding grounds occurring chiefly between March and May (Hayman et al. 1986) (non-breeders may also remain on the wintering grounds all year round) (del Hoyo et al. 1996). When not breeding the species usually forages singly or in small groups (del Hoyo et al. 1996), flying in small parties (Johnsgard 1981) or larger flocks on migration (Flint et al. 1984, Snow and Perrins 1998)and roosting communally at night in mangrove trees or in shallow water (del Hoyo et al. 1996). Habitat Breeding The species breeds on dry scrub heathland (Snow and Perrins 1998), moss and lichen tundra with stunted bushes (Johnsgard 1981), sedge meadows (Johnsgard 1981), wet moorland (del Hoyo et al. 1996, Snow and Perrins 1998) and mossy hummock bogs (Johnsgard 1981, Flint et al. 1984) in open areas, river valleys (del Hoyo et al. 1996), along the shores of tundra lakes (Flint et al. 1984), in birch forest near the Arctic treeline (del Hoyo et al. 1996), burned areas of forest (Flint et al. 1984) and open montane forest (del Hoyo et al. 1996) in the boreal, subarctic and subalpine zones (Johnsgard 1981, del Hoyo et al. 1996). It generally avoids extremes of cold and wet, steep slopes, bare rock and gravel expanses or tall dense vegetation (e.g. dense forest) (Snow and Perrins 1998). Non-breeding On passage in the autumn and spring the species frequents wetlands, tidal flats (del Hoyo et al. 1996), short-sward wet and dry grasslands (Hayman et al. 1986, del Hoyo et al. 1996), farmland (Hayman et al. 1986) and heathland with Empetrum spp., generally occupying coastal habitats in the winter such as muddy, rocky or sandy beaches (del Hoyo et al. 1996), coral shores (Urban et al. 1986), exposed reefs, tidal mudflats (del Hoyo et al. 1996), sandflats (Urban et al. 1986), mangrove swamps (del Hoyo et al. 1996), tidal marshes (Johnsgard 1981) and lagoons (Urban et al. 1986). Diet When inland on migration and during the breeding season its diet consists of adult and larval insects (Johnsgard 1981, del Hoyo et al. 1996) (e.g. Coleoptera, Orthoptera and cranefly larvae), spiders, millipedes, earthworms, snails, slugs, seeds, leaves and berries (del Hoyo et al. 1996) (e.g. of ericaceous plants) (Johnsgard 1981). On the coast during the winter the species takes crustaceans (e.g. crabs), molluscs, large polychaete worms and occasionally fish, reptiles or young birds (del Hoyo et al. 1996). Breeding site The nest is a shallow depression (del Hoyo et al. 1996, Snow and Perrins 1998) often positioned on hummocks or in short heather or grass (Johnsgard 1981, Flint et al. 1984) in dry exposed locations (Johnsgard 1981, Flint et al. 1984, del Hoyo et al. 1996) sometimes far from water (Johnsgard 1981, Flint et al. 1984). When the breeding habitat (e.g. tundra or heathland) is flat and open the species nests in solitary pairs, but where irregular features such as hummocks and tall vegetation patches give more visual isolation the species may nest in loose groups (Snow and Perrins 1998). Management information A study in the Shetland Islands, UK found that when trying to enhance the grazing quality of heathlands by re-seeding (e.g. with high quality grass-seed mixtures) it is better to apply lime, grass-seed and inorganic fertiliser directly to the surface of the ground rather than ploughing and harrowing the ground first, as the latter maintains more natural vegetation hummocks and heather used by the species for nesting (Grant 1992). Re-seeding of heathland with prior ploughing and harrowing may improve feeding conditions for pre-breeding adults however (Grant et al. 1992).|
|Systems:||Terrestrial; Freshwater; Marine|
|Continuing decline in area, extent and/or quality of habitat:||Unknown|
|Generation Length (years):||9.1|
|Movement patterns:||Full Migrant|
|Congregatory:||Congregatory (and dispersive)|
|Major Threat(s):||The species is susceptible to avian influenza so may be threatened by future outbreaks of the virus (Melville and Shortridge 2006).|
|Citation:||BirdLife International. 2012. Numenius phaeopus. The IUCN Red List of Threatened Species 2012: e.T22693178A38790708. http://dx.doi.org/10.2305/IUCN.UK.2012-1.RLTS.T22693178A38790708.en . Downloaded on 09 October 2015.|
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