Data Zone
Justification of Red List category
This species is listed as Critically Endangered because its population has undergone a very rapid reduction, for reasons that are poorly understood but are likely to be at least partly due to hunting along the migration flyway; this decline is projected to continue and increase in the future. Fieldwork in Kazakhstan (and counts in Turkey and the Middle East) has shown the population to be substantially larger than previously feared, but recent demographic studies have found low adult survival, possibly largely driven by hunting pressure along the migration routes and wintering grounds.
Population justification
Surveys in 2006 in Kazakhstan estimated 376 breeding pairs in an area of 145,000 km2. Extrapolating this population density across the breeding range yields a possible total population size of 5,600 breeding pairs, i.e. 11,200 mature individuals, roughly equivalent to 16,000-17,000 individuals in total; but work is continuing in order to refine this estimate. This total is consistent with record counts of 3,200 individuals in Turkey in October 2007 as well as more recent counts on the Uzbekistan/Turkmenistan border where it is estimated that 6,000-8,000 individuals were using the area (Donald et al. 2016). The European population is estimated at 0-10 pairs, which equates to 0-20 mature individuals (BirdLife International 2015).
Trend justification
It has suffered a very rapid decline and range contraction. In northern Kazakhstan, a decline of 40% during 1930-1960, was followed by a further halving of numbers during 1960-1987. However, recent fieldwork in central Kazakhstan (centred on Korgalzhyn), suggests that the population trend is now stable and possibly starting to increase (e.g. the number of nests in a constant survey area around Korgalzhyn increased from 85 in 2005 to 107 in 2006 and 113 in 2007 (Sheldon et al. 2005, M. A. Koshkin, J. Kamp and R. D. Sheldon in litt. 2007); similarly numbers of nests in a constant area of 10,000 km2 around Pavlodar, north-east Kazakhstan were 67 in 1985, 55 in 1991, and 140 in 2007 (J. Kamp in litt. 2007). It is not known if this is a consistent trend across the species's range however, and a global decline of >50% is still precautionarily suspected for the past 27 years (three generations), with an even steeper decline projected for the next three generations owing to potentially severe threats. Further fieldwork may provide data that leads to revision of these estimates. In Europe the population size is estimated to have decreased by 80% or more in 27 years (three generations) and by 25% or more in 9 years (one generation) (BirdLife International 2015).
The species breeds in northern and central Kazakhstan and south-central Russia (and, at least formerly, Xinjiang province, western China [Kamp et al. 2010]), dispersing through Kyrgyzstan, Tajikistan, Uzbekistan, Turkmenistan, Afghanistan, Armenia, Georgia, Azerbaijan, Iran, Iraq, Saudi Arabia, Syria, Turkey and Egypt, to key wintering sites in Sudan (see below), Pakistan (a flock of 28 birds was recorded near Ahmedabad village in Jaffarabad district in 2015 [I. Fisher in litt. 2016]) and north-west India (e.g. 45 birds in the Little Rann of Kutch in November 2007 [Deomurari 2007], 30 at Great Rann of Kutch in November 2008 [J. Tiwari in litt. 2008] and in 2012, a flock of 90 birds was observed [Sheldon 2013]). Small numbers of birds winter regularly in Saudi Arabia, Oman and UAE. There are regular vagrant records in Europe and it has been suggested that a small number of individuals may overwinter in Iberia (de Juana 2011). The species has suffered a very rapid decline and range contraction. In northern Kazakhstan a decline of 40% during 1930-1960 was followed by a further halving of numbers during 1960-1987.
More recent fieldwork has shown the population to be larger than once feared. Surveys in 2006 in Kazakhstan counted 376 breeding pairs in an area of 145,000 km2. Extrapolating this population density across the breeding range yields a possible total population size of 5,600 breeding pairs (Sheldon et al. 2006), i.e. 11,200 mature individuals. A satellite-tagged bird from central Kazakhstan was located in Turkey in October 2007 in a flock of 3,200 individuals (R. Sheldon in litt. 2007, 2008, Biricik 2009). Simultaneous counts made in March 2007 in northern Syria and south-eastern Turkey totalled 1,500-2,000 individuals respectively (Anon. 2007, Bozdogan et al. 2007, Hofland and Keijl 2008). Since then several birds have been tracked to wintering areas in Sudan (P. Donald in litt. 2016), indicating that the sites in the Middle East are used for stopping over en route to Africa. Surveys in September 2009 confirmed the importance of the Manych depression in south Russia as a stopover site with estimates of up to 2,000 individuals (Koshkin 2010). In autumn 2011, 2012 and 2013, 170, 50 and 72 individuals respectively were recorded in the Manych wetlands (Sheldon 2014). However few birds passed through the area in autumn 2015 (V. Fedosov pers. comm. to I. Fisher in litt. 2016), potentially as a result of cold, wet weather. Three satellite tagged birds flew directly across the Caspian Sea, a route previously only seen in the spring (I. Fisher in litt. 2016). Turkey has important stop-over sites at Muş Plain and Ceylanpınar Important Bird Area (1,300 birds were recorded at Ceylanpinar in October 2012 [Sheldon 2014]) (Sheldon et al. 2012). A record flock of more than 400 individuals at Lake Talimarzhan, Uzbekistan in September 2012 suggests that this area is an important staging site for the species (Fowlie 2012). In 2015, 4,225 individuals were recorded in Uzbekistan and 3,675 in Turkmenistan representing the highest numbers of the species recorded anywhere since the 19th century (Donald et al. 2016). The total number of birds using the area was estimated at 6,000-8,000, possibly representing the entirety of the species's eastern flyway population and potentially half of the global population (Donald et al. 2016). Despite survey work, no birds have been located so far in Iraq (Sheldon 2014).
Estimates of productivity and survival on core breeding grounds in central Kazakhstan between 2005-2012 suggest that the population is in slight to severe decline, with a mean annual estimate of population growth rate of 0.81 (95 % C.I. 0.64–0.98), while after five years of relative stability the number of nests in the same area declined rapidly after 2010 (Sheldon et al. 2013). In 2011, 105 nests were located but in 2012 only 44 were found (Sheldon 2013). These low numbers could be due to poor weather conditions during the breeding season (Sheldon 2014). Breeding site fidelity and natal philopatry were low and colonies fluctuated greatly in size between years, making estimation of population trends and survival difficult (Sheldon et al. 2013).
Behaviour This species is migratory (del Hoyo et al. 1996). It breeds semi-colonially in small groups of 3-20 pairs (del Hoyo et al. 1996) from mid-April until July, and begins the migration south in August or September (del Hoyo et al. 1996) (occasionally as late as October [R. Sheldon in litt. 2007, 2008]). Flocks of several thousand birds have been known to gather before migration in Siberia and Kazakhstan (Johnsgard 1981, R. Sheldon in litt. 2007, 2008), but migration itself usually occurs in small groups of 15-20 birds (Johnsgard 1981, del Hoyo et al. 1996). In Syria, it arrives yearly around mid-February to late March, and again in Autumn (Hofland and Keijl 2008). It arrives on its wintering grounds in India and Pakistan by September-October, and in Sudan by late October (del Hoyo et al. 1996). Small flocks of a few to tens of birds are usual on the wintering grounds (Johnsgard 1981), although very occasionally larger flocks of over 100 birds have been recorded (Johnsgard 1981). It departs the wintering grounds in March or early April, arriving on its breeding range from mid April (del Hoyo et al. 1996).
Habitat Breeding It breeds mainly in the transition zones between Stipa and Artemisia grassland steppes where bare saline areas occur near water-bodies. It uses dry wasteland, cultivated, ploughed and stubble fields (del Hoyo et al. 1996). Nests are preferentially placed in areas of Artemisia where there is a high dung abundance and vegetation is short (Watson et al. 2006). Steppes that are densely vegetated may be avoided (Johnsgard 1981), however areas with a low percentage of bare ground and high percentage of tall vegetation are preferred by chicks, and may be important for providing cover from predators (Watson et al. 2006). It has been postulated that it evolved to nest in habitats created by migratory Saiga Saiga tatarica (e.g. Watson et al. 2006), but this is unlikely given the timing of Saiga movements relative to Sociable Lapwing breeding, the speed with which they pass through areas, and the very short swards favoured by the birds; nevertheless Saiga grazing combined with fires may have promoted optimal habitat (Kamp 2007). Suitable habitat probably occurred naturally in sparsely vegetated solonchaks and areas recently burnt by steppe fires, but are now most abundant in the periphery of villages, at least in central Kazakhstan (M. A. Koshkin, J. Kamp and R. D. Sheldon in litt. 2007). Around such villages, there is a strong positive correlation between grazing intensity and the density of nests (Kamp et al. 2009). Non-breeding On migration it uses mainly sandy plains with short grass, dry meadows, fallow land and cultivated fields (del Hoyo et al. 1996). The wintering grounds are burnt steppe and savannah, dry plains, sandy wastes, harvested millet fields, damp pastures and short grass areas, often adjacent to water (del Hoyo et al. 1996). In Arabia it often occurs in the desert near the coast (del Hoyo et al. 1996). Nest survival in central Kazakhstan between 2005 and 2012 was higher closer to human settlements, despite higher trampling rates, and when there were more neighbouring nests, but distance to settlements and colony density both varied systematically between years (Sheldon et al. 2013).
Diet It feeds chiefly on insects including Orthoptera, Coleoptera, and moth larvae (del Hoyo et al. 1996). It also takes arachnids and frequently small amounts of plant matter including grains, leaves and flowers (del Hoyo et al. 1996). Small stones are often found in the stomach, occasionally along with the remains of small vertebrate bones and mollusc shells (del Hoyo et al. 1996). The diet is more varied during the breeding season, being limited mainly to orthopterans and other insects during the non-breeding season (del Hoyo et al. 1996).
Breeding site The nest is a scrape that is unlined or lined with plant material, pebbles and debris (del Hoyo et al. 1996). It is usually found on bare saline patches or in short vegetation near to water (del Hoyo et al. 1996). Nest survival during the egg stage varies between years, owing to varying levels of predation by fox Vulpes vulpes, polecat, long-eared hedgehog and souslik species, and trampling by cattle, and in particular, sheep and goats (M. A. Koshkin, J. Kamp and R. D. Sheldon in litt. 2007).
Illegal hunting during migration and on the wintering grounds may now be the primary threat (M. A. Koshkin, J. Kamp and R. D. Sheldon in litt. 2007, Biricik et al. 2008, Fisher unpublished 2016). Data from 2005-2012 suggest that low adult survival, perhaps resulting from known hunting pressure along the migration routes, appears to be the most critical demographic rate (Sheldon et al. 2013).
Other key factors explaining the magnitude of declines remain poorly understood, despite much recent research. On the breeding grounds, it was probably formerly threatened by the conversion of steppe to arable cultivation, plus, perhaps less likely, the reduction in grazing by large herds of native ungulates and, latterly, by the loss of the enormous herds of domestic grazing animals from state-sponsored collective farms (Eichhorn and Khrokov 2002, Watson et al. 2006). However, since the collapse of the Soviet Union, large areas of arable cultivation have been abandoned and are reverting to natural steppe habitat, herds of domestic livestock have become concentrated around villages (where their permanent presence leads to shorter swards than were created by the vast herds that grazed semi-nomadically under the Soviet system), while an increase in fires (owing to reduced control of fires) may also have contributed to an increase in suitable habitat. These factors may be behind the possible increase in numbers (at least in parts of Kazakhstan) in recent years (Watson et al. 2006, M. A. Koshkin, J. Kamp and R. D. Sheldon in litt. 2007).
Concentration of nests in heavily grazed areas in the vicinity of villages may have increased threats from human disturbance and trampling by sheep, goats and possibly other livestock (Watson et al. 2006, M. A. Koshkin, J. Kamp and R. D. Sheldon in litt. 2007). Low egg survival due to nesting in areas of high grazer density has been suggested as one of the causes for the species' decline (Watson et al. 2006). Nest predation by Rooks Corvus frugilegus - which have expanded widely into the breeding range with the plantation of networks of shelter-belts (Belik 2005) - was previously suggested as a cause of declines, but data from central Kazakhstan indicate this is unlikely (Watson et al. 2006, M. A. Koshkin, J. Kamp and R. D. Sheldon in litt. 2007). The species may be affected by the increasingly dry climate in its breeding and wintering range, but it is not clear if this benefits or threatens this semi-desert species (Watson et al. 2006). Agricultural expansion and intensification, overgrazing and loss of steppe habitats all pose threats to stopover sites used by the species (Ashoori et al. 2013, Sheldon 2013, Asswad 2014). An irrigation project distributing water from the Atatürk dam to fields around Ceylanpinar may have a negative impact on the species as the habitats change (Fisher unpublished 2016).
Conservation Actions Underway
CMS Appendix I and II. An international species action plan was published in 2004. An AEWA International Single Species Action Plan was adopted by the AEWA Meeting of the Parties in May 2012 (Sheldon 2013). It is legally protected in Armenia, Kazakhstan, Russia, Turkmenistan, Ukraine and Uzbekistan, but this is generally not enforced (Belik 2005).
An intensive research project at the breeding sites in central Kazakhstan began in 2004 (Cresswell et al. 2005, Watson et al. 2006), securing funding until 2009 (Anon. 2016). In 2005 the Sociable Lapwing research project was initiated in Kazakhstan by a team from the RSPB and the Association for the Biodiversity Protection in Kazakhstan (ACBK) in order to understand the causes of the species's decline. In 2006 the team secured funding through the UK Government's Darwin Initiative programme that will allow work to continue until 2009. The first co-ordinated count of breeding populations across Kazakhstan was undertaken in 2013, with analysis of the results in progress (Sheldon 2014). A survey of historical breeding sites in the South Urals was conducted in 2005 (Morozov and Kornev 2005) and another at passage sites in south-west Russia was carried out in 2006 (Field et al. 2006). Coordinated counts were undertaken at key passage/wintering sites in Syria and Turkey in March 2007 (Anon. 2007). Due to the current political situation in Syria, structured surveys have not been possible (Sheldon 2014). A project was initiated in Turkey in 2008 to gain a better understanding of stopover sites used by the species during migration (Biricik et al. 2008). Survey work in India was undertaken in 2012-2013 and a local language leaflet was distributed to raise awareness of the species (Sheldon 2013). Further surveys have recently been conducted in Sudan, Turkey (at Ceylanpinar), Iraq, Russia, Pakistan and Uzbekistan (Sheldon 2013). Fields surveys were conducted in Turkey in 2014/2015 and in Russia, Turkmenistan, Uzbekistan and Saudi Arabia in 2015/2016 (Fisher unpublished 2016), and surveys were planned for February 2016 in Pakistan. Surveys on breeding grounds are also planned for 2018 and 2019, using methodologies that would allow for direct comparison with previous surveys (I. Fisher in litt. 2017).
A satellite-tagging project in central Kazakhstan aims to provide information on the species’s migration. Nine birds were tagged in 2010 although their tags are no longer in operation. Three birds were fitted with tags in 2013. Two of the birds migrated via Turkey before wintering in Saudi Arabia and Sudan, the third bird moved eastwards via Turkmenistan/Uzbekistan and Afghanistan before wintering in Pakistan (Sheldon 2014). Three more birds were tagged in June 2014 (Anon. 2015a), a further three in June 2015 (Anon. 2015b) and five more tags were planned to be fitted in August 2015 (Anon. 2015c). Of the nine birds with tags migrating in autumn 2015, two flew via Talimarjan to winter in Pakistan, four flew directly across the Caspian Sea (three wintering in Sudan, one lost contact in Russia), and the remainder travelled across the top of the Caspian Sea, down through Turkey, and into the Middle East and North Africa (I. Fisher in litt. 2016). Updates on their movements are posted on the Amazing Journey website (http://www.birdlife.org/sociable-lapwing/).
Hunting in Syria has been identified as a major threat with measures being implemented to control it. Nature Iraq have been engaging with hunters and conducting awareness raising activities in Iraq (Sheldon 2013).
The inaugural meeting of the International Sociable Lapwing Working Group was held in Palmyra, Syria in March 2011. The group agreed on conservation measures required by each country, and planned cross-border actions to protect the species across its extensive range. A large area around Ceylanpinar was designated as a no hunting zone in 2015 (Fisher unpublished 2016).
Conservation Actions Proposed
Continue research in Kazakhstan (and initiate in Russia) on breeding biology, habitat requirements and migration, including colour-ringing and satellite tracking to determine movements. Continue surveys of breeding range in Kazakhstan, potential breeding range in Russia and western China, and wintering/passage sites in Middle East and Africa (including determining periods when birds are present). Continue to monitor trends on breeding grounds and at key passage/winter sites. Identify and evaluate key threats on breeding, passage and wintering grounds. Ensure that all Important Bird Areas where the species is a feature are legally protected (Sheldon 2013). Investigate the importance of hunting on passage/wintering grounds. Review International Species Action Plan in the light of recent research on the breeding grounds and identification of key passage/wintering sites. Develop national species action plans, at least for Kazakhstan and key passage/wintering countries. At breeding colonies sensitive to trampling by sheep during nesting period, work with local shepherds to minimise disturbance. Control hunting on wintering/passage sites.
27-30 cm. Strikingly patterned plover. Adult greyish with black and chestnut belly. White supercilium and black crown and eye-stripe. Winter adult brownish but retains supercilium and crown pattern. Juvenile brown, slightly scalloped above, and streaked black below with large white supercilium. Similar spp. White-tailed Lapwing V. leucurus lacks supercilium and crown patch, has longer legs and no black subterminal tail-band. Voice Harsh kretsch kretsch and a rapid chattering.
Text account compilers
Pople, R., Symes, A., Ashpole, J, Wheatley, H., Calvert, R., Butchart, S., Benstead, P., Ekstrom, J., Pilgrim, J.
Contributors
Al-Jbour, S., Balkiz, O., Donald, P., Hofland, R., Kamp, J., Khrokov, V., Koshkin, M., Morozov, V., Sheldon, R., Tavares, J. & Fisher, I.
Recommended citation
BirdLife International (2024) Species factsheet: Sociable Lapwing Vanellus gregarius. Downloaded from
https://datazone.birdlife.org/species/factsheet/sociable-lapwing-vanellus-gregarius on 25/12/2024.
Recommended citation for factsheets for more than one species: BirdLife International (2024) IUCN Red List for birds. Downloaded from
https://datazone.birdlife.org/species/search on 25/12/2024.