
TOP > 生物多様性センターの国際協力 > ESABII > Database > Migrant Birds Database > Terek Sandpiper
Common Name | Terek SandpiperBirdlife International | |||||||||||||||||||||||||||||||||||||||||||||
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Species name | Xenus cinereusBirdlife International | |||||||||||||||||||||||||||||||||||||||||||||
Family | Scolopacidae | |||||||||||||||||||||||||||||||||||||||||||||
Genus | ||||||||||||||||||||||||||||||||||||||||||||||
Local Name |
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No descriptions
No descriptions
This species is a full migrant1. The East Asian population migrates along the eastern coast of the continent, whereas the populations in western Asia pass south overland through the Caspian region, the Middle East1 or between the Ural and Volga rivers2. The Finnish population flies across Eastern Europe and crosses the Mediterranean and Sahara non-stop1. Breeding occurs between May and June1, after which the adults depart in early-July (the juveniles departing mainly in August)2, to arrive in their wintering grounds between August and October3. The return movement northward from Africa begins in late-March and continues throughout April2. Many one-year-old3 and other non-breeding birds remain in the wintering grounds throughout the northern summer1. This species is known to breed semi-collonially1 (as many as 10 nests have been found within a square kilometer)4, but is mainly solitary outside of the breeding season2. Occasionally it occurs in small flocks of 5-25 individuals1, or up to 300 at tidal roosting sites3. The species is both a diurnal and nocturnal forager, but its nocturnal activities may by restricted to moonlit nights8.
<Breeding> This species breeds in lowland valleys in northern boreal forest and tundra, especially on floodplains with flooded meadows and marshes, and where overgrown moist grasslands alternate with willow scrub1, 2. It also frequents lakesides and marshy banks of streams, and extends to the coasts of sheltered seas in the Baltic2. The species avoids mountains, fast rocky streams, steep or broken terrain, extensive open spaces and tall dense forest2.
<Non-breeding> Outside of the breeding season the species inhabits tropical coasts, especially open intertidal estuaries and mudflats, as well as coral reefs, sandy and pebbly beaches, sandbars and mudlfats at river mouths, coastal swamps, saltpans1, coastal lagoons and saltmarsh creeks4. It can occasionally also be found up to 10 km inland around brackish pools and riverbeds, and often forms communal roosts in the branches of mangroves1. During migration the species may stop-over at inland freshwater wetlands1, such as muddy lakes or river edges3.
<Breeding> On its breeding grounds the diet of this species consists mainly of adult and larval midges (Diptera) as well as seeds1.
<Non-breeding> In its wintering grounds and on migration the diet of this species is more varied, consisting of a variety of insects, small molluscs, crustaceans (including crabs), spiders and annelid worms1.
The nest is a shallow depression close to water either in the open, or sheltered by short grasses3.
1. del Hoyo et al. (1996). 2. Snow and Perrins (1998). 3. Urban et al. (1986). 4. Johnsgard (1981). 5. Barter (2002). 6. Barter (2006). 7. Tanabe et al. (1998). 8. Rohweder and Baverstock (1996).
LC
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.
<Trend justification> The overall population trend is stable, although some populations have unknown trends (Wetlands International 2006).
Country | Category | Reference |
---|---|---|
Brunei Darussalam | ||
Cambodia | ||
China | ||
Indonesia | ||
Japan | ||
Korea | ||
Lao PDR | ||
Malaysia | ||
Mongolia | ||
Myanmar | ||
Philippines | ||
Singapore | ||
Thailand | ||
Vietnam |
In China and South Korea important migrational staging areas of this species around the coast of the Yellow Sea are being lost through land reclamation, and degraded as a result of declining river flows (from water abstraction), increased pollution, unsustainable harvesting of benthic fauna and a reduction in the amount of sediment being carried into the area by the Yellow and Yangtze Rivers5, 6. This species is also potentially at risk from exposure to DDT's in southern India7.
No descriptions
No descriptions
No descriptions
Country | Status | Reference |
---|---|---|
Brunei Darussalam | ||
Cambodia | ||
China | ||
Indonesia | ||
Japan | ||
Korea | ||
Lao PDR | ||
Malaysia | Protected Wild Birds Part I: Game Birds(as Tringa terek) | Law of Malaysia Act 76, Protection of Wild Life Act 1972 (Amend. 2006) |
Mongolia | ||
Myanmar | ||
Philippines | ||
Singapore | ||
Thailand | ||
Vietnam |
The Asian Waterbird Census (AWC) was initiated in 1987 and runs in parallel with other waterbird censuses carried out in Africa, Europe, Central and West Asia and Latin America under the umbrella of the International Waterbird Census (IWC), which is organised by Wetlands International.
The AWC takes place annually, during the second and third weeks of January, and is carried out by volunteers interested in collecting information on waterbirds and wetlands as a basis for contributing to their conservation.
Reference: Li, Z.W.D., Bloem, A., Delany S., Martakis G. and Quintero J. O. 2009. Status of Waterbirds in Asia - Results of the Asian Waterbird Census: 1987-2007. Wetlands International, Kuala Lumpur, Malaysia
BRUNEI DARUSSALAM | 1986 | 1987 | 1988 | 1989 | 1990 | 1991 | 1992 | 1993 | 1994 | 1995 | 1996 | 1997 | 1998 | 1999 | 2000 | 2001 | 2002 | 2003 | 2004 | 2005 | 2006 | 2007 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
The number of observed individual | ||||||||||||||||||||||
The number of observed sites(not all count sites) | ||||||||||||||||||||||
The total number of count sites | 2 | 3 | 3 | 2 | 4 | 4 | 0 | 4 | 4 | 4 | 4 | 5 | 5 | 0 | 0 | 0 | 9 | 0 | 0 | 1 | 0 | 9 |
CAMBODIA | 1986 | 1987 | 1988 | 1989 | 1990 | 1991 | 1992 | 1993 | 1994 | 1995 | 1996 | 1997 | 1998 | 1999 | 2000 | 2001 | 2002 | 2003 | 2004 | 2005 | 2006 | 2007 |
The number of observed individual | 136 | |||||||||||||||||||||
The number of observed sites(not all count sites) | 1 | |||||||||||||||||||||
The total number of count sites | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 4 | 0 | 0 | 11 | 0 | 0 | 12 | 12 | 11 | 5 | 1 | 6 | 9 | 6 | 6 |
CHINA | 1986 | 1987 | 1988 | 1989 | 1990 | 1991 | 1992 | 1993 | 1994 | 1995 | 1996 | 1997 | 1998 | 1999 | 2000 | 2001 | 2002 | 2003 | 2004 | 2005 | 2006 | 2007 |
The number of observed individual | 115 | 16 | 10 | 10 | 3 | 2 | ||||||||||||||||
The number of observed sites(not all count sites) | 1 | 1 | 1 | 1 | 1 | 1 | ||||||||||||||||
The total number of count sites | 0 | 1 | 34 | 12 | 50 | 60 | 67 | 29 | 6 | 14 | 6 | 15 | 21 | 20 | 14 | 10 | 22 | 45 | 80 | 81 | 59 | 72 |
INDONESIA | 1986 | 1987 | 1988 | 1989 | 1990 | 1991 | 1992 | 1993 | 1994 | 1995 | 1996 | 1997 | 1998 | 1999 | 2000 | 2001 | 2002 | 2003 | 2004 | 2005 | 2006 | 2007 |
The number of observed individual | 1050 | 167 | 33 | 226 | 47 | 401 | 13 | 397 | 50 | 39 | 91 | |||||||||||
The number of observed sites(not all count sites) | 1 | 4 | 1 | 2 | 3 | 3 | 1 | 3 | 1 | 2 | 1 | |||||||||||
The total number of count sites | 0 | 0 | 0 | 1 | 19 | 8 | 17 | 17 | 15 | 19 | 16 | 0 | 0 | 47 | 12 | 10 | 40 | 34 | 14 | 16 | 15 | 23 |
JAPAN | 1986 | 1987 | 1988 | 1989 | 1990 | 1991 | 1992 | 1993 | 1994 | 1995 | 1996 | 1997 | 1998 | 1999 | 2000 | 2001 | 2002 | 2003 | 2004 | 2005 | 2006 | 2007 |
The number of observed individual | 1 | 1 | 8 | 12 | 16 | 70 | ||||||||||||||||
The number of observed sites(not all count sites) | 1 | 1 | 4 | 2 | 2 | 3 | ||||||||||||||||
The total number of count sites | 0 | 0 | 0 | 53 | 39 | 52 | 47 | 20 | 50 | 40 | 47 | 37 | 41 | 37 | 107 | 112 | 103 | 109 | 97 | 159 | 142 | 137 |
LAO PDR | 1986 | 1987 | 1988 | 1989 | 1990 | 1991 | 1992 | 1993 | 1994 | 1995 | 1996 | 1997 | 1998 | 1999 | 2000 | 2001 | 2002 | 2003 | 2004 | 2005 | 2006 | 2007 |
The number of observed individual | ||||||||||||||||||||||
The number of observed sites(not all count sites) | ||||||||||||||||||||||
The total number of count sites | 0 | 0 | 0 | 2 | 4 | 5 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | 0 | 14 | 1 | 0 | 0 | 0 | 1 | 0 | 0 |
MALAYSIA | 1986 | 1987 | 1988 | 1989 | 1990 | 1991 | 1992 | 1993 | 1994 | 1995 | 1996 | 1997 | 1998 | 1999 | 2000 | 2001 | 2002 | 2003 | 2004 | 2005 | 2006 | 2007 |
The number of observed individual | 2692 | 3217 | 4611 | 4120 | 466 | 860 | 110 | 203 | 313 | 277 | 226 | 660 | 287 | 375 | 1478 | 5649 | 1330 | |||||
The number of observed sites(not all count sites) | 25 | 23 | 27 | 31 | 9 | 3 | 3 | 3 | 4 | 7 | 3 | 6 | 11 | 11 | 27 | 26 | 10 | |||||
The total number of count sites | 0 | 0 | 0 | 59 | 68 | 93 | 85 | 17 | 10 | 7 | 10 | 0 | 0 | 20 | 25 | 25 | 25 | 43 | 43 | 82 | 82 | 40 |
MYANMAR | 1986 | 1987 | 1988 | 1989 | 1990 | 1991 | 1992 | 1993 | 1994 | 1995 | 1996 | 1997 | 1998 | 1999 | 2000 | 2001 | 2002 | 2003 | 2004 | 2005 | 2006 | 2007 |
The number of observed individual | 5 | 16 | 3 | 40 | 227 | |||||||||||||||||
The number of observed sites(not all count sites) | 1 | 1 | 1 | 1 | 9 | |||||||||||||||||
The total number of count sites | 0 | 5 | 3 | 12 | 17 | 15 | 21 | 20 | 13 | 12 | 2 | 4 | 2 | 0 | 7 | 32 | 47 | 73 | 24 | 31 | 32 | 19 |
PHILIPPINES | 1986 | 1987 | 1988 | 1989 | 1990 | 1991 | 1992 | 1993 | 1994 | 1995 | 1996 | 1997 | 1998 | 1999 | 2000 | 2001 | 2002 | 2003 | 2004 | 2005 | 2006 | 2007 |
The number of observed individual | 191 | 79 | 318 | 274 | 350 | 213 | 108 | 212 | 154 | 218 | 495 | 273 | 96 | 233 | 300 | 473 | 343 | 366 | ||||
The number of observed sites(not all count sites) | 9 | 5 | 15 | 13 | 20 | 12 | 13 | 5 | 12 | 15 | 22 | 11 | 10 | 16 | 12 | 12 | 15 | 24 | ||||
The total number of count sites | 0 | 0 | 0 | 0 | 19 | 21 | 34 | 39 | 46 | 47 | 39 | 28 | 29 | 32 | 43 | 38 | 50 | 47 | 56 | 54 | 65 | 108 |
SINGAPORE | 1986 | 1987 | 1988 | 1989 | 1990 | 1991 | 1992 | 1993 | 1994 | 1995 | 1996 | 1997 | 1998 | 1999 | 2000 | 2001 | 2002 | 2003 | 2004 | 2005 | 2006 | 2007 |
The number of observed individual | 44 | 43 | 16 | 99 | 25 | 15 | 49 | 14 | 55 | 17 | 10 | 70 | 23 | 2 | 5 | 20 | 8 | |||||
The number of observed sites(not all count sites) | 1 | 4 | 4 | 3 | 3 | 3 | 4 | 2 | 5 | 4 | 2 | 3 | 2 | 1 | 1 | 1 | 3 | |||||
The total number of count sites | 0 | 0 | 0 | 0 | 4 | 12 | 17 | 15 | 13 | 14 | 10 | 10 | 6 | 11 | 10 | 10 | 8 | 9 | 9 | 8 | 8 | 7 |
REPUBLIC OF KOREA | 1986 | 1987 | 1988 | 1989 | 1990 | 1991 | 1992 | 1993 | 1994 | 1995 | 1996 | 1997 | 1998 | 1999 | 2000 | 2001 | 2002 | 2003 | 2004 | 2005 | 2006 | 2007 |
The number of observed individual | ||||||||||||||||||||||
The number of observed sites(not all count sites) | ||||||||||||||||||||||
The total number of count sites | 0 | 0 | 10 | 12 | 22 | 20 | 20 | 15 | 10 | 22 | 25 | 22 | 14 | 68 | 99 | 112 | 118 | 116 | 117 | 123 | 127 | 127 |
THAILAND | 1986 | 1987 | 1988 | 1989 | 1990 | 1991 | 1992 | 1993 | 1994 | 1995 | 1996 | 1997 | 1998 | 1999 | 2000 | 2001 | 2002 | 2003 | 2004 | 2005 | 2006 | 2007 |
The number of observed individual | 123 | 1 | 300 | 166 | 154 | 2 | 5 | 202 | 3 | 36 | 127 | 178 | ||||||||||
The number of observed sites(not all count sites) | 2 | 1 | 1 | 5 | 3 | 1 | 1 | 2 | 1 | 3 | 4 | 4 | ||||||||||
The total number of count sites | 10 | 8 | 3 | 20 | 26 | 12 | 23 | 16 | 17 | 5 | 9 | 3 | 1 | 1 | 7 | 3 | 9 | 26 | 20 | 82 | 99 | 33 |
VIETNAM | 1986 | 1987 | 1988 | 1989 | 1990 | 1991 | 1992 | 1993 | 1994 | 1995 | 1996 | 1997 | 1998 | 1999 | 2000 | 2001 | 2002 | 2003 | 2004 | 2005 | 2006 | 2007 |
The number of observed individual | 1 | 1 | 2 | |||||||||||||||||||
The number of observed sites(not all count sites) | 1 | 1 | 2 | |||||||||||||||||||
The total number of count sites | 0 | 0 | 0 | 1 | 2 | 0 | 1 | 4 | 0 | 1 | 1 | 0 | 1 | 8 | 2 | 2 | 16 | 4 | 4 | 9 | 6 | 11 |