EN
Milky Stork Mycteria cinerea



Taxonomy

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. Volume 1: Non-passerines. Lynx Edicions BirdLife International, Barcelona, Spain and Cambridge, UK.

IUCN Red List criteria met and history
Red List criteria met
Critically Endangered Endangered Vulnerable
A2bcd+4bcd A2bcd+3bcd+4bcd; C2a(ii) A2bcd+3bcd+4bcd; C2a(i); D1

Red List history
Year Category Criteria
2023 Endangered A2bcd+3bcd+4bcd; C2a(ii)
2016 Endangered A2cd+3cd+4cd
2013 Endangered A2cd+3cd+4cd
2012 Vulnerable A2cd+3cd+4cd
2008 Vulnerable A2c,d; A3c,d; A4c,d
2006 Vulnerable
2004 Vulnerable
2000 Vulnerable
1996 Vulnerable
1994 Vulnerable
1988 Threatened
Species attributes

Migratory status not a migrant Forest dependency medium
Land-mass type continent
shelf island
Average mass -
Range

Estimate Data quality
Extent of Occurrence (breeding/resident) 3,200,000 km2 medium
Extent of Occurrence (non-breeding) 3,500,000 km2 medium
Severely fragmented? no -
Population
Estimate Data quality Derivation Year of estimate
Population size 600-1850, 1200-1850 mature individuals medium estimated 2023
Population trend decreasing poor inferred 1995-2025
Rate of change over the past 10 years/3 generations (longer of the two periods) 40-86,50-79% - - -
Rate of change over the future 10 years/3 generations (longer of the two periods) 25-70% - - -
Rate of change over the past & future 10 years/3 generations (longer of the two periods) 40-86,50-79% - - -
Generation length 9.87 years - - -
Number of subpopulations 3 - - -
Percentage of mature individuals in largest subpopulation 84-96% - - -

Population justification:

The population size of this species is considered to be immensely depleted. Countries of occurrence are discussed (approximately) north to south: In Cambodia, it is considered a very rare resident (Goes 2013, CBGA 2019) with most birds at the Prek Toal colony (17 pairs in 2010, 4-5 more recently but stable: Goes 2013, S. Mahood in litt. 2023). In Thailand, small numbers of non-breeding individuals occur in the Pak Thale area (western side of the Bay of Bangkok) and Huai Chorakhe Mak Reservoir Non-hunting Area (eBird 2023), but these likely sum to fewer than 10 individuals, none of which are known to breed in the country and probably originate from the Prek Toal colony in neighbouring Cambodia. In Malaysia, the current situation is opaque. The species is thought to have been extirpated (MNS Conservation Council 2021) or declined to '<5 individuals' (Ismail and Rahman 2016, Puan et al. 2020), but has been subject to various and sporadic reintroduction attempts since 1998. After March 2007, this captive-breeding attempt increased in intensity (Ismail and Rahman 2016) with recent records from Kuala Gula Bird Sanctuary and Kuala Selangor (eBird 2023). However, there is no indication that there is yet a self-sustaining population in Malaysia, despite best efforts, and the population size here (in any instance unlikely to comprise more than 20-30 mature individuals) is not considered part of the wild population. Some birds visiting the west coast of Peninsula Malaysia, however, might be wanderers from neighbouring Sumatra (wild) or Singapore (feral). In the latter, there is a small but frequently-reported population that comprises at least 50 birds (eBird 2023), which sometimes cross over into neighbouring Malaysia. A high percentage of this population are known to be hybrids (with M. leucucephala) (Baveja et al. 2019) and the population is believed to have originated from escapes rather than a deliberate introduction for conservation; they are consequently not considered in the number of wild mature individuals.

The species' stronghold remains in Indonesia, particularly the eastern mangroves of Sumatra, which may now constitute the only viable population (Baveja et al. 2019). In 2009, the first and only comprehensive population estimate of the species in Sumatra since the 1990s (see BirdLife International 2001) was made, recording c.1,600 birds as follows: c.75 individuals in Aceh province, c.500 North Sumatra province, c.350 Riau province, c.100 Jambi province, c.500 South Sumatra province and c.75 Lampung province. Not all of these are likely to have been mature individuals, and there is evidence that the species has continued to decline since then, although perhaps at a rate slower than since the 1990s (M. Iqbal in litt. 2023); the current population is probably somewhere between 800 and 1,600 birds. The population on Java is assumed to be small, with only two breeding sites confirmed in recent years: (1) Pulau Dua, Banten, which has only recently been re-occupied and from which only a handful of birds are known (Noor et al. 2020); and (2) Pulau Rambut Wildlife Sanctuary, which between 2017-2020 hosted 11-70 birds (Y. R. Noor pers. obs., in Noor et al. 2020). In 2017, 73 Mycteria cinerea were also observed at a colony of 20 nests in Indramayu, West Java, although no chicks were observed (Noor et al. 2020). During the ‘Big Month’ citizen science event (conducted in January 2020 comprising 22,054 checklists) across Java and Bali moreover, the species was recorded in only 21 (0.26%) of the 7,935 tetrads (2 × 2 km2 squares) visited, amounting to an estimated 131 individuals based on maximum counts for nine coastal locations on Java and Madura (T. Squires and S. Marsden in litt. 2020). Compiling data, it is considered unlikely that Java hosts more than 50 breeding pairs, although numbers at key sites may be augmented by non-breeding individuals. Finally, on Sulawesi, c.100-150 birds have been observed in Rawa Aopa Watumohai National Park (M. Iqbal pers. obs., 2014) but here too recent data are lacking except for a flock of 10 observed in February 2016 (eBird 2023); there are no records on Sulawesi away from this area, or from Sumbawa, despite historic observations (BirdLife International 2001, eBird 2023).

Adding these total is difficult owing to uncertainty between the ratio of individuals to mature individuals. Overall, the population outside Indonesia is now negligible. On Sumatra, the current number of mature individuals is suspected to lie somewhere between c. 500-1,600 (with scenarios ranging from population stability since censuses in 2009, to continued population reductions). On Java and Sulawesi, the combined total is unlikely to be more than 100-200 mature individuals, thus the global population is assumed to number 600-1,850 mature individuals, with a best estimate of 1,200-1,850 on the basis that declines may recently have slowed (M. Iqbal in litt. 2023).

Trend justification:

This species’ population is suspected to have declined rapidly over the past three generations (30 years: 1993-2023) and while rates of decline may have slowed, there is no sign of population recovery, and the species' (now relatively small) population continues to decrease. The trend in each range state is discussed, broadly from north to south: In Cambodia, has evidently always been scarce and confined to a single site, Tonle Sap, which hosts the only inland breeding colony of this species in the world (BirdLife International 2001, Goes 2013). Apparently 15 known pairs in 1996 (Parr et al. 1996), and numbers varied 2002-2012 between two and 17 visible pairs (Goes 2013). Numbers are apparently still stable at 4-5 pairs with a similar number of birds in hybridising pairs with M. leucocephala (S. Mahood in litt. 2023). Over the last three generations there may therefore have been a slight reduction, although numbers now seem stable, and Cambodia has always hosted only a small percentage of this species' global population. In Thailand, there is no evidence it ever bred (BirdLife International 2001) and the number of non-breeding visitors each year is very small, with no plausible hope of elucidating trends; it is consequently not discussed further.  In Peninsular Malaysia, numbers fell from counts of over 100 individuals in 1984, to fewer than 10 birds in 2005, and only a single wild bird in 2010 (Malaysian Nature Society 2005, Li et al. 2006, DWNP 2010). No wild birds remain, and contemporary sightings of this species in Malaysia originate from zoo escapes (either from Kuala Lumpur, or neighbouring Singapore) and (apparently failed) reintroduction attempts (see Ismail and Rahman 2016 for summary; also Puan et al. 2020, eBird 2023).

The majority of the global population now exists in Indonesia, where trends are undoubtedly the most significant in a global context. Here rapid declines are well evidenced in response to intense hunting pressure at nesting colonies and the rapid loss and conversion of coastal habitat. Numbers on Sumatra, which holds more a large majority of the global population, fell from 5,000 birds in 1986 (Silvius 1988, Silvius and Verheugt 1989) to 1,600 in 2009, a 68% decrease (Iqbal et al. 2008, Iqbal et al. 2012). In Java, a wintering flock in east Madura of 170+ birds observed in 1996 had diminished to c.70 birds in 2006, which may be representative of an island-wide decline (B. van Balen in litt. 2013); there are very few recent records from here, except for two birds in February 2021 and seven in January 2023 (eBird 2023), potentially suggesting declines here have continued, but coverage has been very poor. Elsewhere in Java, historic data are too poor to speculate on past and future trends. Trends on Sulawesi are similarly unknown. Since 2009, population declines on Sumatra may have slowed. Data to confirm this are poor, but the population in south Sumatra province, for example, is suspected to have fallen to 300-400 in 2023, down from an estimate of c. 500 in 2009 (M. Iqbal in litt. 2023).

In the early- to mid-1990s, Perennou et al. (1994) and Rose and Scott (1997) estimated a global population of 6,100 birds (not all of which will have referred to mature individuals, and assuming a ratio of 0.5-0.7 of breeding birds, will have been equivalent to approximately 3,000-4,300 mature individuals). The contemporary population size estimate of 600-1,850 mature individuals (with a best estimate of 1,200-1,850) therefore suggests that has been a reduction equivalent to 40-86% over the past three generations. Using a methodology that extrapolates likely rates of decline based only on Sumatran data suggests a decline equivalent to 77% over three generations up to 2009, but with indications that declines, while ongoing, may have slowed slightly since then (M. Iqbal in litt. 2023). Accordingly, the overall rate of population reduction over the past three generations is set at 40-86%, with a best estimate of 50-79%.


Country/territory distribution
Country/Territory Presence Origin Resident Breeding visitor Non-breeding visitor Passage migrant
Cambodia extant native yes yes
Indonesia extant native yes
Malaysia extant introduced yes
Singapore extant introduced yes
Thailand extant native yes

Important Bird and Biodiversity Areas (IBA)
Country/Territory IBA Name
Cambodia Ang Tropeang Thmor
Cambodia Prek Taek Sap
Cambodia Prek Toal
Cambodia Sre Ambel
Cambodia Stung Kampong Smach
Cambodia Stung Sen / Santuk / Baray
Indonesia Bali Barat
Indonesia Berbak
Indonesia Bukit Barisan Selatan
Indonesia Danau Tempe
Indonesia Feruhumpenai - Matano
Indonesia Kerumutan
Indonesia Morowali
Indonesia Muara Angke
Indonesia Muara Cimanuk
Indonesia Muara Gembong - Tanjung Sedari
Indonesia Pesisir Pantai Jambi
Indonesia Pesisir Riau Tenggara
Indonesia Pesisir Timur Pantai Sumatera Utara
Indonesia Pulau Dua
Indonesia Pulau Rambut
Indonesia Rawa Aopa Watumohai
Indonesia Rawa Tulang Bawang
Indonesia Segara Anakan - Nusa Kambangan
Indonesia Sembilang
Indonesia Siak Kecil
Indonesia Solo Delta
Indonesia Sumenep
Indonesia Taliwang
Indonesia Tanjung Koyan
Indonesia Tanjung Selokan
Indonesia Way Kambas
Malaysia Matang coast
Malaysia North-central Selangor coast
Malaysia South-west Johor coast

Habitats & altitude
Habitat (level 1) Habitat (level 2) Importance Occurrence
Artificial/Aquatic & Marine Artificial/Aquatic - Water Storage Areas (over 8ha) suitable non-breeding
Artificial/Terrestrial Arable Land suitable non-breeding
Forest Subtropical/Tropical Mangrove Vegetation Above High Tide Level major breeding
Forest Subtropical/Tropical Moist Lowland suitable breeding
Marine Coastal/Supratidal Coastal Brackish/Saline Lagoons/Marine Lakes major non-breeding
Wetlands (inland) Permanent Freshwater Lakes (over 8ha) major non-breeding
Wetlands (inland) Permanent Freshwater Marshes/Pools (under 8ha) major non-breeding
Altitude 0 - 200 m Occasional altitudinal limits (max) 1000 m

Threats & impact
Threat (level 1) Threat (level 2) Impact and Stresses
Agriculture & aquaculture Annual & perennial non-timber crops - Agro-industry farming Timing Scope Severity Impact
Ongoing Majority (50-90%) Slow, Significant Declines Medium Impact: 6
Stresses
Ecosystem degradation, Ecosystem conversion
Agriculture & aquaculture Marine & freshwater aquaculture - Industrial aquaculture Timing Scope Severity Impact
Ongoing Majority (50-90%) Slow, Significant Declines Medium Impact: 6
Stresses
Ecosystem degradation, Ecosystem conversion
Biological resource use Hunting & trapping terrestrial animals - Intentional use (species is the target) Timing Scope Severity Impact
Ongoing Majority (50-90%) Rapid Declines Medium Impact: 7
Stresses
Species mortality
Biological resource use Logging & wood harvesting - Unintentional effects: (subsistence/small scale) [harvest] Timing Scope Severity Impact
Ongoing Majority (50-90%) Slow, Significant Declines Medium Impact: 6
Stresses
Ecosystem degradation
Human intrusions & disturbance Work & other activities Timing Scope Severity Impact
Ongoing Majority (50-90%) Slow, Significant Declines Medium Impact: 6
Stresses
Species disturbance
Invasive and other problematic species, genes & diseases Problematic native species/diseases - Mycteria leucocephala Timing Scope Severity Impact
Future Unknown Unknown Unknown
Stresses
Hybridisation
Residential & commercial development Commercial & industrial areas Timing Scope Severity Impact
Ongoing Minority (<50%) Slow, Significant Declines Low Impact: 5
Stresses
Ecosystem degradation, Ecosystem conversion
Residential & commercial development Housing & urban areas Timing Scope Severity Impact
Ongoing Majority (50-90%) Slow, Significant Declines Medium Impact: 6
Stresses
Ecosystem degradation, Ecosystem conversion

Utilisation
Purpose Scale
Food - human subsistence, national
Pets/display animals, horticulture subsistence, national

Recommended citation
BirdLife International (2024) Species factsheet: Milky Stork Mycteria cinerea. Downloaded from https://datazone.birdlife.org/species/factsheet/milky-stork-mycteria-cinerea on 22/11/2024.
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 22/11/2024.