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.
Critically Endangered | Endangered | Vulnerable |
---|---|---|
- | - | C2a(ii) |
Year | Category | Criteria |
---|---|---|
2020 | Vulnerable | C2a(ii) |
2016 | Endangered | C2a(i) |
2012 | Endangered | C2a(i) |
2008 | Endangered | C2a(i) |
2004 | Endangered | |
2000 | Endangered | |
1996 | Vulnerable | |
1994 | Vulnerable | |
1988 | Threatened |
Migratory status | full migrant | Forest dependency | high |
Land-mass type |
continent |
Average mass | - |
Estimate | Data quality | |
---|---|---|
Extent of Occurrence (breeding/resident) | 1,010,000 km2 | medium |
Extent of Occurrence (non-breeding) | 1,440,000 km2 | medium |
Number of locations | 11-100 | - |
Severely fragmented? | no | - |
Estimate | Data quality | Derivation | Year of estimate | |
---|---|---|---|---|
Population size | 5000-9999 mature individuals | poor | suspected | 2014 |
Population trend | decreasing | poor | inferred | 2010-2026 |
Rate of change over the past 10 years/3 generations (longer of the two periods) | 1-9% | - | - | - |
Rate of change over the future 10 years/3 generations (longer of the two periods) | 1-9% | - | - | - |
Rate of change over the past & future 10 years/3 generations (longer of the two periods) | 1-9% | - | - | - |
Generation length | 5.5 years | - | - | - |
Number of subpopulations | 1 | - | - | - |
Percentage of mature individuals in largest subpopulation | 100% | - | - | - |
Population justification: Previous work in Japan suggests the assertion that the global population comprises fewer than 1,000 individuals may have been overly pessimistic. These estimations are however not considered accurate by some researchers (K. Kawakami in litt. 2016). Recent mating call detections however recorded 23 individuals per 100 km2 in rural secondary forests across the Aichi Prefecture in central Japan (Hamaguchi et al. 2014). The total area of rural secondary forests in Honshu, Kyushu and Shikoku islands estimates to 72,000 km2 (Watanabe et al. 2012). Thus, the number of mature individuals is thought to be approximately 8,280. However, mating call detection studies have been considered as an unreliable method of monitoring breeding numbers in this instance due to the species's inconspicuous habits and the potential of receiving duplicated records (K. Ohata in litt. 2020). Similar calling surveys have for example not recorded any nests, and as such breeding birds, despite observing other calling individuals. It is also likely that surveys specific to limited sites (the Aichi area in this instance), may not yield results that are compatible with other suitable habitats across the species's range (K. Ohata in litt. 2020). Habitat models have additionally been considered impractical methods of estimating population numbers or trends (J. Kushlan in litt. 2020). Hence, to account for any uncertainty, the true figure is placed here in the band of 5,000-9,999 mature individuals, roughly equating to 7,500-15,000 individuals. As per the Waterbird Population Estimates, the species is also thought to occur in only one flyaway population across Eastern and South-eastern Asia (Wetlands International 2020). This is assumed to represent one subpopulation holding all mature individuals.
Trend justification: The species had previously considered to have undergone rapid declines due to deforestation and habitat conversion (Martinez-Vilalta et al. 2020). However, recent forest loss estimates show a negligible decline (Tracewski et al. 2016, Global Forest Watch 2020), equating to 3% over three generations (16.5 years; Bird et al. 2020). Forest destruction is also considered to no longer be a threat across breeding sites in Japan (S. Chan in litt. 2020). However, the population is thought to be rapidly declining at migratory and wintering grounds (S. Chan in litt. 2020), primarily owed to hunting pressure. Breeding areas may also suffer from problematic native and non-native species, as well as some level of continued habitat degradation. Thus, the population is inferred to be undergoing a continued decline of 1-9% over three generations.
Country/Territory | Presence | Origin | Resident | Breeding visitor | Non-breeding visitor | Passage migrant |
---|---|---|---|---|---|---|
Brunei | extant | vagrant | yes | |||
China (mainland) | extant | native | yes | yes | ||
Hong Kong (China) | extant | native | yes | |||
Indonesia | extant | vagrant | yes | |||
Japan | extant | native | yes | |||
Palau | extant | vagrant | yes | |||
Philippines | extant | native | yes | |||
Russia | extant | vagrant | yes | |||
Russia (Asian) | extant | vagrant | yes | |||
South Korea | extant | native | yes | yes | ||
Taiwan, China | extant | native | yes | |||
Vietnam | extant | vagrant |
Country/Territory | IBA Name |
---|---|
Indonesia | Tangkoko Dua Sudara |
Indonesia | Mahawu - Masarang |
Philippines | University of the Philippines Land Grants (Pakil and Real) |
Philippines | Quezon National Park |
Philippines | Victoria and Anepahan Ranges |
Philippines | Central Panay mountains |
Philippines | Cuernos de Negros |
Philippines | Mount Bandila-an |
Philippines | Mount Hilong-hilong |
Philippines | Mount Kampalili-Puting Bato |
Philippines | Mount Hamiguitan (Tumadgo peak) |
Philippines | Liguasan marsh |
Philippines | Mount Busa-Kiamba |
Philippines | Mount Latian complex |
Philippines | Pasonanca watershed |
Philippines | Mount Malindang |
Japan | Hachirogata |
Japan | Mount Hyonosen |
Habitat (level 1) | Habitat (level 2) | Importance | Occurrence |
---|---|---|---|
Artificial/Terrestrial | Arable Land | suitable | non-breeding |
Forest | Subtropical/Tropical Dry | suitable | non-breeding |
Forest | Subtropical/Tropical Dry | suitable | breeding |
Forest | Subtropical/Tropical Moist Lowland | major | non-breeding |
Forest | Subtropical/Tropical Moist Lowland | major | breeding |
Forest | Subtropical/Tropical Moist Montane | major | non-breeding |
Forest | Subtropical/Tropical Moist Montane | major | breeding |
Forest | Temperate | major | breeding |
Wetlands (inland) | Bogs, Marshes, Swamps, Fens, Peatlands | suitable | non-breeding |
Altitude | 0 - 2400 m | Occasional altitudinal limits |
Threat (level 1) | Threat (level 2) | Impact and Stresses | |||||||
---|---|---|---|---|---|---|---|---|---|
Agriculture & aquaculture | Annual & perennial non-timber crops - Shifting agriculture | Timing | Scope | Severity | Impact | ||||
Ongoing | Majority (50-90%) | Rapid Declines | Medium Impact: 7 | ||||||
|
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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 | ||||||
|
|||||||||
Biological resource use | Logging & wood harvesting - Unintentional effects: (subsistence/small scale) [harvest] | Timing | Scope | Severity | Impact | ||||
Ongoing | Majority (50-90%) | Rapid Declines | Medium Impact: 7 | ||||||
|
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Energy production & mining | Renewable energy | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Slow, Significant Declines | Low Impact: 5 | ||||||
|
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Geological events | Volcanoes | Timing | Scope | Severity | Impact | ||||
Past, Likely to Return | Minority (<50%) | Rapid Declines | Past Impact | ||||||
|
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Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Mustela sibirica | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Slow, Significant Declines | Low Impact: 5 | ||||||
|
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Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Unspecified species | Timing | Scope | Severity | Impact | ||||
Ongoing | Majority (50-90%) | Slow, Significant Declines | Medium Impact: 6 | ||||||
|
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Invasive and other problematic species, genes & diseases | Problematic native species/diseases - Cervus nippon | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Causing/Could cause fluctuations | Low Impact: 5 | ||||||
|
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Residential & commercial development | Commercial & industrial areas | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Slow, Significant Declines | Low Impact: 5 | ||||||
|
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Residential & commercial development | Housing & urban areas | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Slow, Significant Declines | Low Impact: 5 | ||||||
|
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Residential & commercial development | Tourism & recreation areas | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Slow, Significant Declines | Low Impact: 5 | ||||||
|
Purpose | Primary form used | Life stage used | Source | Scale | Level | Timing |
---|---|---|---|---|---|---|
Food - human | - | - | non-trivial | recent | ||
Handicrafts, jewellery, etc. | - | - | non-trivial | recent | ||
Pets/display animals, horticulture | - | - | international | non-trivial | recent |
Recommended citation
BirdLife International (2023) Species factsheet: Gorsachius goisagi. Downloaded from
http://datazone.birdlife.org/species/factsheet/japanese-night-heron-gorsachius-goisagi on 11/12/2023.
Recommended citation for factsheets for more than one species: BirdLife International (2023) IUCN Red List for birds. Downloaded from
http://datazone.birdlife.org on 11/12/2023.