Tawny Eagle Aquila rapax Scientific name definitions
Text last updated September 6, 2015
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Species names in all available languages
Language | Common name |
---|---|
Afrikaans | Roofarend |
Arabic | عقاب صحماء |
Bulgarian | Блед орел |
Catalan | àguila rapaç |
Croatian | savanski orao |
Czech | orel okrový |
Danish | Rovørn |
Dutch | Savannearend |
English | Tawny Eagle |
English (United States) | Tawny Eagle |
Finnish | savannikotka |
French | Aigle ravisseur |
French (France) | Aigle ravisseur |
German | Savannenadler |
Greek | Αμμόχρωμος Στεπαετός |
Hebrew | עיט סוואנות |
Hungarian | Szavannasas |
Icelandic | Hræörn |
Italian | Aquila rapace |
Japanese | アフリカソウゲンワシ |
Lithuanian | Stepinis erelis |
Marathi | पिंगट गरुड |
Norwegian | savanneørn |
Persian | عقاب خاکی |
Polish | orzeł sawannowy |
Portuguese (Angola) | Águia-fulva |
Portuguese (Portugal) | Águia-fulva |
Romanian | Acvilă de savană |
Russian | Саванный орёл |
Serbian | Savanski orao |
Slovak | orol bronzový |
Slovenian | Roparski orel |
Spanish | Águila Rapaz |
Spanish (Spain) | Águila rapaz |
Swedish | savannörn |
Thai | นกอินทรีสีน้ำตาล |
Turkish | Korsan Kartal |
Ukrainian | Орел рудий |
Aquila rapax (Temminck, 1828)
Definitions
- AQUILA
- aquila
- rapax
The Key to Scientific Names
Legend Overview
Field Identification
60–75 cm (1); 1600–3100 g (1); wingspan 159–183 cm (1). Mid-sized to large eagle, with longish neck, but relatively short wings and slightly rounded to almost square-ended tail (1). Smaller, paler and with shallower gape than A. nipalensis. Polymorphic (1) and individually variable in intensity of colour and extent of markings. Iris yellow amber. Female larger (by up to 15% (1) ) and usually darker and more heavily marked than male. Juvenile more plainly coloured, especially ventrally, and plumage fades to blond; often rather redder. Races differ on size, and also on markings and extent of rufous coloration, but considerable individual variation and extensive overlap; vindhiana smaller, generally tends to be darker, lacks tawny, and sometimes, perhaps always, has brown iris; <em>belisarius</em> shares most plumage types with nominate race (notably very pale immature), but tends not to appear so scruffy.
Systematics History
Editor's Note: This article requires further editing work to merge existing content into the appropriate Subspecies sections. Please bear with us while this update takes place.
Recent phylogenetic analyses indicated that this species forms a monophyletic group with A. nipalensis and A. heliaca (presumably also A. adalberti) (2). Has in the past been considered conspecific with A. nipalensis, but the two differ in morphology, behaviour and ecology, and treatment as separate species supported by molecular analysis (3). Race vindhiana has been considered a separate species, but limited differences do not support this. Three subspecies normally recognized.Subspecies
Aquila rapax belisarius Scientific name definitions
Distribution
Aquila rapax belisarius (Levaillant, 1850)
Definitions
- AQUILA
- aquila
- rapax
- belisarius
The Key to Scientific Names
Legend Overview
Aquila rapax rapax Scientific name definitions
Distribution
Aquila rapax rapax (Temminck, 1828)
Definitions
- AQUILA
- aquila
- rapax
The Key to Scientific Names
Legend Overview
Aquila rapax vindhiana Scientific name definitions
Distribution
Aquila rapax vindhiana Franklin, 1831
Definitions
- AQUILA
- aquila
- rapax
- vindhiana
The Key to Scientific Names
Legend Overview
Distribution
Editor's Note: Additional distribution information for this taxon can be found in the 'Subspecies' article above. In the future we will develop a range-wide distribution article.
Habitat
Open woodland, wooded savannah, semi-desert (1) and arid steppe; only absent from forest and true desert. Often found near villages and cultivation in India, where it visits rubbish dumps and slaughterhouses (1). In Nepal, virtually restricted to terai. Recorded from sea level to 3000 m, but principally found in lowlands (1).
Movement
Resident in most areas but perhaps some seasonal movement into more arid areas in SW and NE Africa during the rainy season; also some birds perform seasonal N–S movements in W Africa (moving S in Oct–Nov and N in Apr (1) ). Often mixes with flocks of migrant A. nipalensis. Rare vagrant in W of range, where it has has wandered N to Algeria, Tunisia, Italy, Egypt, Israel (five records, some race belisarius, mostly in winter, once Aug) (1, 4), Iran and Oman (unclear if race belisarius or vindhiana involved) (5). Frequently listed in handbooks and checklists as having occurred as a vagrant in SE Asia, but historical records from Myanmar have proven to be erroneous, a specimen from Thailand has recently been re-identified as a juvenile A. fasciata, and two records from Tonkin (Vietnam) are equally unacceptable (a specimen also pertains to A. fasciata and a sight record seems likely to have been misidentified); nevertheless, two recent sight records from Myanmar (in Jan 2000 and Oct 2005), while not confirmed, do suggest that the species might occasionally wander to this region (6).
Diet and Foraging
Mammals (to size of hares and dikdiks) (1), birds (including gamebirds such as francolins, guineafowl and bustards, as well as hornbills) (1, 7) and lizards form bulk of catholic diet. May also take carrion (to size of elephants (1) ) with vultures, Milvus migrans (5) and A. nipalensis (8), insects (many termites , especially in non-breeding season (1) ), amphibia and fish when available. Remains of domestic chickens found in nests (5). Dives on prey (as large as flamingos (1) ) from a perch or stoops while soaring high overhead, but may also walk about collecting food on the ground (including at rubbish dumps (5) and slaughterhouses (1) ). Observed predating Stresemann’s Bushcrow (Zavattariornis stresemanni) nest (9). Regularly and boldly steals from other birds such as storks, other raptors and ground hornbills (Bucorvus), and also reported apparently following hunting dogs (Lycaon pictus) presumably to scavenge prey (10).
Sounds and Vocal Behavior
A rather hollow barking “kau-kau” or similar is most typical; also higher-pitched “ki-ark” given by male in display, when grating “kekeke...” also heard, and mewing “shreep-shreep” given by female at nest. Although not especially vocal is considered to be more so than Palearctic wintering in Africa (1).
Breeding
Lays in dry season: Sept–Feb (11) in NE Africa (but mainly from Nov in Ethiopia (9) ); Oct–Feb in W Africa; Mar–Oct in E Africa (peak May–Jul); Apr–Sept in S & C Africa; Nov–Mar in India. Suspected year-round in SW Arabia, but eggs only recorded Dec–Jan in this region (5). Both sexes (mainly female) (12) build large (1) platform of sticks 90–130 cm (12) across and 30 cm deep (but even larger with extensive reuse) (1), lined with grass, leaves and fur (1), on the crown of a thorny tree (usually Acacia) (1) 5–30 m above ground (13), the only African eagle to do so regularly; in relatively treeless areas, rarely nests on a power pylon (a phenomenon first noticed in 1970s) (13), and, mainly in India, near villages (1). Pairs usually spaced at intervals of 4–6 km (13). Often nests in vicinity of watering point for game or stock, and frequently reuses same nest in subsequent seasons, although pairs may also build new nest just a few hundred metres away (13). Usually two white eggs, unmarked or have faint brown or reddish-brown markings (12) (1–3), laid at three-day intervals (13), size 69–71 mm × 54–55 mm (12); incubation 39–46 days (1), from initiation of clutch, mainly by female (13); chicks initially have white to pale grey down (but second coat is denser and greyer) (12); eldest chick frequently kills younger sibling; fledging 76–85 days (1), but young remain dependent for an additional c. 6 weeks (1). Sometimes lays replacement clutch if first attempt fails early (13).
Conservation Status
VULNERABLE. CITES II. Formerly common in many areas, including several large national parks, such as Comoé (Ivory Coast), Hwange (Zimbabwe) with an estimated 200 pairs, and Kruger (South Africa) with 292 pairs, at least in past. Once commonest eagle of Indian plains. Very uncommon in Nepal, where presumed to be resident. Status in Myanmar unknown: probably only a vagrant; possibly very rare resident, e.g. along R Irrawaddy. No confirmed records in Bangladesh (14). Adaptable, breeding equally successfully at mean inter-nest spacing of 3·5–59 km and densities of 1 pair/64–300 km². Scavenging habits make it susceptible to poisoning and has declined in many farming areas of S & E Africa. Also declining in W & NE Africa , and may now be largely absent from large areas of W Africa outside conservation units (15). Not known to be affected by pesticides.