Nisaetus cirrhatus

The changeable hawk-eagle or crested hawk-eagle (Nisaetus cirrhatus) is a large bird of prey species of the family Accipitridae. More informal or antiquated English common names include the marsh hawk-eagle or Indian crested hawk-eagle. It is a member of the booted eagle subfamily, with signature feathers, absent in tropical raptors from outside this subfamily, covering the tarsus. It was formerly placed in the genus Spizaetus, but studies pointed to the group being paraphyletic resulting in the Old World members being placed in Nisaetus (Hodgson, 1836) and separated from the New World species. It is a typical “hawk-eagle” in that it is an agile forest-dwelling predator and like many such eagles readily varies its prey selection between birds, mammals or reptiles as well as other vertebrates. Among the members of its genus, the changeable hawk-eagle stands out as the most widely distributed, adaptable and abundant species. The taxonomy of the wide ranging changeable hawk-eagle is complex and confusing, with few authorities agreeing on whether the species in fact houses a species complex. Gamauf et al. (2005) analyzed mtDNA cytochrome b and control region sequence data of a considerable number of specimens of the crested hawk-eagle and some relatives. Despite the large sample, even the most conspicuous dichotomy - that between the crested and crestless groups - was not as well resolved as it might have been expected to be. At least one widely accepted genetic study has resulted in a recent revision to the recognition of a new species, as the Flores hawk-eagle has traditionally been treated as a subspecies of the changeable hawk-eagle, but it is now often treated as a separate species, N. floris. The Flores and changeable hawk-eagles are regarded as sister species. The three small-island taxa (N. c. andamanensis, N. c. vanheurni, and N. floris) as a whole each appear as monophyletic lineages. Their placement is even more unresolved, with N. floris being apparently a very ancient lineage. The other two seem quite certainly to derive from N. c. limnaeetus. The latter taxon has a confusing phylogeny. Different lineages exist that are apparently not stable in space and time, are best described as polytomy, from which the similar island taxa derive. Obviously, N. c. limnaeetus does not represent a monophyletic lineage. Neither the biological nor the phylogenetic species concepts, nor phylogenetic systematics can be applied to satisfaction. The crested group apparently is close to becoming a distinct species. The island taxa derived from N. c. limnaeetus appear to have undergone founder effects, which has restricted their genetic diversity. In the continental population, genetic diversity is considerable, and the evolutionary pattern of the two studied genes did not agree, and neither did the origin of specimens show clear structures. N. c. limnaeetus thus is best considered a metapopulation. Gamauf et al. (2005) therefore suggest the island taxa which are obviously at higher risk of extinction are, for conservation considered evolutionary significant units regardless of their systematic status. This case also demonstrates that a too-rigid interpretation of cladistics and the desire for monophyletic taxa, as well as universal application of single-species concept to all birds will undermine correct understanding of evolutionary relationships. It would even not be inconceivable to find mainland lineages to group closely with the western island taxa, if little genetic drift had occurred in the initial population. nonetheless, the divergence of this species' lineages seems to have taken place too recently to award them species status, as compared to the level of genetic divergence at which clades are usually considered distinct species. N. c. limnaeetus appears for all that can be said with reasonable certainty basal pool of lineages in the crestless group that, despite not being monophyletic, should be considered a valid taxon as long as gene flow is possible through its range. In addition, as ancient DNA from museum specimens was used extensively, the possibility of ghost lineages must be considered. If it is assumed that all or most of the ancient lineages still exist today, considerable recombination must have taken place as the two genes' phylogenies do not agree much, indicating a healthy level of gene flow. Whether this still holds true today remains to be determined. Two distinct groups exist in the changeable hawk-eagle; one with crests and one without or with hardly visible crests. Dark morphs exist for some populations. Changeable hawk-eagle Crestless changeable hawk-eagle The changeable hawk-eagle is a largish but slender eagle. They fall near the middle of sizes among the currently accepted species in the genus Nisaetus. As in most birds of prey, females are larger than males with an average overall size difference of 7% but this can individually range to an 18-22% difference, with island races apparently thought to be less dimorphic on average. Size is quite variable and total length has been reported in the past to vary from 51 to 82 cm (20 to 32 in) and wingspan from 100 to 160 cm (3 ft 3 in to 5 ft 3 in), however these figures appear to include the much more massive hawk-eagles from Flores that are currently considered their own separate species by modern authorities. Nonetheless, total lengths of up to 77 cm (30 in) have been listed for N. c. limnaeetus in Nepal. Ali & Ripley (1978) estimated these average total lengths for the following subspecies: N. c. cirrhatus at 72 cm (28 in), N. c. limnaeetus at 70 cm (28 in) and N. c. andamanensis at 61 cm (24 in). Legge (1880) measured the length of Sri Lankan changeable hawk-eagles (N. c. ceylanensis) without including the beak as 55 to 60 cm (22 to 24 in). The average length of birds from the Philippines (N. c. limnaeetus) was measured as 58.4 cm (23.0 in) in males and 64.9 cm (25.6 in) in females. Weights in this species have been reported from 1.2 to 1.9 kg (2.6 to 4.2 lb) but the source of this is unclear and it probably underrepresents the size variation known to occur in the species. The only precise body masses known for the species are derived from the Philippine population, where males were found to average 1.36 kg (3.0 lb) while females averaged 1.6 kg (3.5 lb) but they could weigh in excess of 1.81 kg (4.0 lb). Adult changeable hawk-eagles are typically dark brown above and boldly streaked below with a strong bill, a variably sized, often floppy crest or no crest, rather short wings, a quite long, thinly-barred tail and long feathered legs. This species tends to perch “bolt” upright, and may perch in various places from somewhat secluded spots to also quite open area as well. When perched, their wings reach only about one-third to half way down tail. Pale morph adults are mainly dark brown above with very faint paler edges (usually only conspicuous on the wing-coverts). They tend to have an evenly black-streaked and somewhat rufous-tinged head and neck, with a blackish crest (if present). The tail tends to be paler brown than the back with a thin whitish tip, a broad, blackish subterminal band (both the whitish tip and the subterminal band are also visible from tail underside) and 3 to 4 narrower, brown and often rather obscure bars. On the pale morph hawk-eagle’s underside, the base colour is white to buff overlaid with bold black to dark brown streaking; the streaking tends to be more subtle on abdomen but more obvious on the legs. Beyond the typical pale morph, some subspecies but especially N. c. liminaeetus tend to have a further intermediate and a dark morph. The intermediate morph is somewhat similar to pale morph adults but is heavily grey-brown below with little to no paler base colour showing and more obscure streaking, with the area from belly down to the crissum usually being unpatterned. Meanwhile, the dark morph adult can range from all dark chocolate brown to almost pure black with variable browner edges, relieved only by the greyish inner half of tail as well as some greyish tail bars. Most juvenile changeable hawk-eagles are dark brown above but with far more conspicuous white edges on mantle and wings than the adults, in some cases, the median coverts are largely white and greater and even lesser coverts are largely scaled with white. The juvenile has a light brown tail with about seven thin dark bars and a whitish tip. The young hawk-eagle’s head varies from buff with white-tipped black crest (as is the case in peninsular India and Sri Lanka) through entirely whitish, but almost always the young birds are spotted and streaked with black or dark brown about the rear crown and nape. As is the head, the underparts are variable with juveniles in much of India and in Sri Lanka showing thin brown streaks on chest or small spots on breast, with obscure tawny barring on thigh, legs and crissum. Juveniles elsewhere are often nearly all pure whitish below. By the time the young hawk-eagles reaches their 2nd to 3rd year, they tend to show less white above and more brown or black below. Their tail starts to molt to resemble that of adults in the 3rd year but in the 2nd year in N. c. limnaeetus (or at least in Philippines). Changeable hawk-eagles may attempt to breed at 3 years of age but full adult plumage is not obtained until the 4th year. Adults have yellow to orange yellow eyes, while those of the juvenile are grey-brown to pale greenish. Adult have a cere that’s grey to pale greenish yellow and juveniles’ ceres are dull greyish, while all ages have yellow feet.