
TOP > 生物多様性センターの国際協力 > ESABII > Database > Migrant Birds Database > Caspian Plover
Common Name | Caspian PloverBirdlife International | |||||||||||||||||||||||||||||||||||||||||||||
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Species name | Charadrius asiaticusBirdlife International | |||||||||||||||||||||||||||||||||||||||||||||
Family | Charadriidae | |||||||||||||||||||||||||||||||||||||||||||||
Genus | ||||||||||||||||||||||||||||||||||||||||||||||
Local Name |
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No descriptions
No descriptions
This species is fully migratory1. It migrates to winter in African between August and October, and once within Africa moves south in a nomadic fashion following the dry season1. The species departs from southern Africa in late-February to early March, and from East and south-east Africa in late-March to early-April, frequenting stop-over sites in Iran, Iraq, the Arabian Peninsula and the Red Sea (it over-flies this Middle Eastern region during the Autumn migration), arriving in the breeding grounds again from late-March to early-May1. On migration the species usually moves in flocks of 5-12 (and sometimes up to 30) individuals, and whilst over-wintering in Africa it moves in Nomadic flocks of 5-20 individuals1. When breeding this species may nest singly or in small loose colonies of 10-25 pairs spaced at least 50-60 m apart1.
<Breeding> This species breeds in desert and desert steppe near water amongst sparse shrub vegetation1 up to about 800 m7. It is primarily associated with saline habitats such as salt-pans, saline soils subject to seasonal flooding1, inland saltmarshes5 and alkali flats6. The species concentrates in flocks after breeding but whilst still in its breeding range on the banks of lakes, rivers, water-holes trampled by cattle1, and cultivated land4.
<Non-breeding> In its non-breeding range (Africa) the species is often found far from water on recently burnt or heavily grazed grassland, dry floodplains, ploughed cultivated land, coastal dunes (Somalia)1, 2, 3, the dried mud of lake shores4, salt-pans, saltmarshes,3 airfields and golf courses (where it is attracted by insects on animal droppings)1. During migration the species has been recorded on damp sandbanks and pebble beds along the Zambezi River, Zimbabwe3.
The species is primarily carnivorous throughout both the breeding and non-breeding seasons.
<Breeding> Whilst breeding the species takes mainly adult and larval insects1, 5 such as beetles, ants, grasshoppers, bugs, caterpillars and flies, although it will occasionally take plant material (e.g. grass seeds)1.
<Non-breeding> During the non-breeding season beetles, termites, grasshoppers and small snails are the main contributors to this species diet, and it is often observed hunting for insects in town refuse heaps and cattle dung1.
The nest of this species is a shallow scrape on open ground or amongst low vegetation1.
1. del Hoyo et al. (1996). 2. Urban et al. (1986). 3. Hockey et al. (2005). 4. Hayman et al. (1986). 5. Johnsgard (1981). 6. Flint et al. (1984). 7. Snow and Perrins (1998).
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). 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 may be moderately small to large, but it is not believed to 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 population is suspected to be in decline owing to ongoing habitat destruction (del Hoyo et al. 1996).
Country | Category | Reference |
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Brunei Darussalam | ||
Cambodia | ||
China | ||
Indonesia | ||
Japan | ||
Korea | ||
Lao PDR | ||
Malaysia | ||
Mongolia | ||
Myanmar | ||
Philippines | ||
Singapore | ||
Thailand | ||
Vietnam |
The main threat to this species is the destruction of natural steppe and grassland though overgrazing and conversion to intensive agricultural practices, especially within the European (breeding) part of its range1.
No descriptions
No descriptions
No descriptions
Country | Status | Reference |
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Brunei Darussalam | ||
Cambodia | ||
China | ||
Indonesia | ||
Japan | ||
Korea | ||
Lao PDR | ||
Malaysia | ||
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 | ||||||||||||||||||||||
The number of observed sites(not all count sites) | ||||||||||||||||||||||
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 | ||||||||||||||||||||||
The number of observed sites(not all count sites) | ||||||||||||||||||||||
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 | ||||||||||||||||||||||
The number of observed sites(not all count sites) | ||||||||||||||||||||||
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 | ||||||||||||||||||||||
The number of observed sites(not all count sites) | ||||||||||||||||||||||
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 | ||||||||||||||||||||||
The number of observed sites(not all count sites) | ||||||||||||||||||||||
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 | ||||||||||||||||||||||
The number of observed sites(not all count sites) | ||||||||||||||||||||||
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 | ||||||||||||||||||||||
The number of observed sites(not all count sites) | ||||||||||||||||||||||
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 | ||||||||||||||||||||||
The number of observed sites(not all count sites) | ||||||||||||||||||||||
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 | ||||||||||||||||||||||
The number of observed sites(not all count sites) | ||||||||||||||||||||||
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 | ||||||||||||||||||||||
The number of observed sites(not all count sites) | ||||||||||||||||||||||
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 |