NT
Grey-headed Fish-eagle Icthyophaga ichthyaetus



Taxonomy

Taxonomic note
The genus Icthyophaga (del Hoyo and Collar 2014) was previously spelled Ichthyophaga.

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
- - -

Red List history
Year Category Criteria
2024 Near Threatened A2cde+3cde+4cde
2016 Near Threatened A2cd+3cd+4cd; C1+2a(i)
2012 Near Threatened A2cd+3cd+4cd; C1+2a(i)
2008 Near Threatened A2b,c; A3b,c; A4b,c; C1
2004 Near Threatened
2000 Lower Risk/Near Threatened
1994 Lower Risk/Near Threatened
1988 Lower Risk/Least Concern
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) 16,200,000 km2 medium
Severely fragmented? no -
Population
Estimate Data quality Derivation Year of estimate
Population size unknown - - -
Population trend decreasing poor suspected 2000-2030
Rate of change over the past 10 years/3 generations (longer of the two periods) 20-29% - - -
Rate of change over the future 10 years/3 generations (longer of the two periods) 20-29% - - -
Rate of change over the past & future 10 years/3 generations (longer of the two periods) 20-29% - - -
Generation length 9.92 years - - -

Population justification: There is little information on the population size of I. ichthyaetus. However, the population is likely not considerably large despite its expansive range (Ferguson-Lees and Christie 2001). The species is considered rare and/or local in Nepal and Sri Lanka, uncommon and local in Bangladesh (Grimmett et al. 1998), and rare and scarce in Myanmar, Philippines, Cambodia and Singapore (Robson 2000, BirdLife International 2001); it may now be extirpated entirely from Lao PDR (Timmins et al. in press). The species is considered rare across most of South-East Asia (Ferguson-Lees and Christie 2001). The species is absent from the north and centre of Thailand, and disappearing from the north of Vietnam (from which there are almost no recent records: eBird 2024) and it is considered scarce in southern Thailand and Vietnam (Robson 2000). In Indonesia it is widely distributed but uncommon in Sumatra and Borneo (MacKinnon and Phillipps 1993). North-east India likely represents a stronghold for the species where it is considered widespread and frequent (Grimmett et al. 1998, Ferguson-Lees and Christie 2001).

There have however been few efforts to quantify population sizes. Several areas along the Mekong river in Cambodia were estimated to hold dozens of breeding pairs (Bezuijen et al. 2008), although the numbers appear to have drastically declined in Cambodia in recent years (Mittermeier et al. 2019). Miron and Chowdhury (2019) recorded 0.54 birds/km2 in Noakhali District, Bangladesh, and Tingay et al. (2006) recorded one breeding pair every 2.5 km2 in Tonle Sap Lake, Cambodia. These two studies demonstrate two regions that support sufficient food sources and consequentially localised and abundant breeding populations. However, given the species is likely to congregate in preferred breeding habitat, and there is little known about its abundance across much of its range, it is not possible to extrapolate these estimates to provide an estimation of the total population size. Therefore, the population size is unknown.

Trend justification:

I. ichthyaetus is widespread but has suffered declines across most of its range. The species was formally widespread in the lowlands of Lao PDR, but has declined rapidly as a result of habitat loss and degradation (Fuchs et al. 2007, Timmins et al. in press) to the extent that the species may have become extinct in the country (Timmins et al. in press) or persists only in very small numbers (Thewlis et al. 1998, Fuchs et al. 2007, Bezuijen et al. 2008). Similar declines in Cambodia are also critical for the species, with at least two regionally significant breeding populations present along the Kratie to Lao PDR section of the Mekong (Bezuijen et al. 2008) and at Prek Toal, Tonya Sap Lake (Tingay et al. 2010). Three surveys carried out throughout 2007 along 130 km of riverine and floodplain habitat along the Mekong River recorded 150 sightings of an expected 40-60 breeding pairs (Bezuijen et al. 2008), but the species was only recorded once when the same region was revisited 10 years later (Mittermeier et al. 2019). The region was reportedly seriously impacted by human interference from selective logging for charcoal production and clearing for agriculture (Mittermeier et al. 2019, BirdLife International 2024). A logging company was also observed actively building roads and extracting timber (Mittermeier et al. 2019). Further impacts to the species likely include unsustainable fishing practices, such as poisoning which can lead to direct mortality, as well as explosives which can contribute to declining food sources (BirdLife International 2024). In comparison, surveys between 2005 and 2009 at Prek Toal recorded 60-80 occupied nests annually (Tingay et al. 2012), suggesting a reasonably stable breeding population. Although there have not been recent surveys of this population, the species is still frequently and consistently recorded at Prek Toal (eBird 2024) suggesting numbers are persisting. This population is threatened by the unsustainable harvesting of water snakes (a primary food source) by the local human population (Tingay et al. 2006, 2010) as well as the upstream construction of hydro-electric dams in Cambodia, as well as China, Laos, and Thailand which may disrupt the flood cycle at Prek Toal (Kummu and Sarkkula 2008) and increase mercury accumulation in food sources which can lead to reproductive failure (Jagoe et al. 2002). Severe declines are also suspected to be occurring in Indonesia, particularly in Sumatra where it was thought to be fairly numerous in the 1980s and 1990s (Holmes and Noor 1995, Clarke et al. 2023). The declines are at least partly attributable to the cage bird trade (Nijman et al. 2022, TRAFFIC 2024) but on Sumatra have probably been largely driven by the conversion of large areas of lowland forest to oil-palm and rubber plantations (Descal et al. 2021, Wang et al. 2023). The species is also declining in Thailand where it was formally widespread, Vietnam where it is rapidly disappearing from the north, Malaysia with only an estimated 40 pairs on the peninsula, as well as Philippines, and Cambodia (Robson 2000, Ferguson-Lees and Christie 2001, Fuchs et al. 2007, Clarke et al. 2023).

Conversely, populations in other regions appear to be stable, despite disturbance or highly modified areas in some cases. For example, the species is considered widespread and frequently encountered in north-east India (Clarke et al. 2023). Additionally, the species has stably bred in small numbers over several years in Chitwan, Nepal, despite overfishing, habitat loss and degradation, and pollution of waterways all cited as causes of waterbird declines in the region (BCN and DNPWC 2011, Adhikari et al. 2018). Provided there is a sufficient food source for the species, it appears that even human modified habitat can support large breeding densities. Miron and Chowdhury (2019) recorded 0.54 birds/km2 in Noakhali District, Bangladesh, an area with a high density of commercial fisheries, as well as human settlements and agricultural areas (Miron and Chowdhury 2019). The study found c. 77% of nests within 100 m of human settlements and c. 73% closer to commercial rather than non-commercial waterbodies. These numbers are comparable to breeding densities in Tonle Sap Lake, Cambodia (a natural swamp forest with little human disturbance; Tingay et al. [2010]) of one pair every 2.5km2 (Tingay et al. 2006), suggesting that the species can persist in disturbed areas as long as suitable nesting trees and food sources are present. Furthermore, the species may be increasing in abundance in Singapore (Clarke et al. 2023) due to this adaptability to urban waterbodies and the introduced prey items (Yong 2011).

There has been an estimated 28-33% loss of forest cover within the species range over the past-three generations (Global Forest Watch 2024, based on data from Hansen et al. [2013] and methods disclosed therein). However, forest loss alone is likely to overestimate population declines considering the species’ adaptability to modified areas (Yong 2011, Miron and Chowdhury 2019). Consequentially, continuing declines in the range of 20-29% are suspected.


Country/territory distribution
Country/Territory Presence Origin Resident Breeding visitor Non-breeding visitor Passage migrant
Bangladesh extant native yes
Bhutan extant native yes
Brunei extant native yes
Cambodia extant native yes
India extant native yes
Indonesia extant native yes
Laos extant native yes
Malaysia extant native yes
Myanmar extant native yes
Nepal extant native yes
Philippines extant native yes
Singapore extant native yes
Sri Lanka extant native yes
Thailand extant native yes
Vietnam extant native yes

Important Bird and Biodiversity Areas (IBA)
Country/Territory IBA Name
Nepal Barandabhar forests and wetlands
Nepal Bardia National Park
Nepal Chitwan National Park
Nepal Koshi Tappu Wildlife Reserve and Koshi Barrage
Nepal Sukla Phanta Wildlife Reserve
Vietnam Kon Cha Rang
Vietnam Pu Mat
Vietnam Yok Don

Habitats & altitude
Habitat (level 1) Habitat (level 2) Importance Occurrence
Artificial/Aquatic & Marine Artificial/Aquatic - Aquaculture Ponds suitable resident
Artificial/Aquatic & Marine Artificial/Aquatic - Water Storage Areas (over 8ha) suitable resident
Marine Coastal/Supratidal Coastal Freshwater Lakes major resident
Marine Neritic Estuaries suitable resident
Wetlands (inland) Bogs, Marshes, Swamps, Fens, Peatlands suitable resident
Wetlands (inland) Permanent Freshwater Lakes (over 8ha) major resident
Wetlands (inland) Permanent Rivers/Streams/Creeks (includes waterfalls) major resident
Altitude 0 - 1500 m Occasional altitudinal limits  

Threats & impact
Threat (level 1) Threat (level 2) Impact and Stresses
Agriculture & aquaculture Wood & pulp plantations - Agro-industry plantations Timing Scope Severity Impact
Ongoing Majority (50-90%) Slow, Significant Declines Medium Impact: 6
Stresses
Ecosystem degradation, Ecosystem conversion
Biological resource use Fishing & harvesting aquatic resources - Unintentional effects: (subsistence/small scale) [harvest] Timing Scope Severity Impact
Ongoing Majority (50-90%) Slow, Significant Declines Medium Impact: 6
Stresses
Indirect ecosystem effects
Biological resource use Hunting & trapping terrestrial animals - Intentional use (species is the target) Timing Scope Severity Impact
Ongoing Minority (<50%) Slow, Significant Declines Low Impact: 5
Stresses
Reduced reproductive success, Species mortality
Biological resource use Hunting & trapping terrestrial animals - Persecution/control Timing Scope Severity Impact
Ongoing Majority (50-90%) Slow, Significant Declines Medium Impact: 6
Stresses
Species mortality
Natural system modifications Dams & water management/use - Large dams Timing Scope Severity Impact
Ongoing Majority (50-90%) Slow, Significant Declines Medium Impact: 6
Stresses
Ecosystem degradation, Ecosystem conversion
Pollution Industrial & military effluents - Type Unknown/Unrecorded Timing Scope Severity Impact
Ongoing Majority (50-90%) Slow, Significant Declines Medium Impact: 6
Stresses
Species mortality

Utilisation
Purpose Scale
Pets/display animals, horticulture national, international

Recommended citation
BirdLife International (2024) Species factsheet: Grey-headed Fish-eagle Icthyophaga ichthyaetus. Downloaded from https://datazone.birdlife.org/species/factsheet/grey-headed-fish-eagle-icthyophaga-ichthyaetus on 23/11/2024.
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 23/11/2024.