TABLE 39. MEASUREMENTS OF _Rhipidura lepida_

================+=========+=========+=============+=============

Number and Sex | Wing | Tail | Culmen | Tarsus

----------------+---------+---------+-------------+-------------

7 adult males | 80 | 89 | 15.5 | 23.3

| (77-83) | (85-94) | (14.5-16.0) | (23.0-24.0)

| | | |

7 adult females | 77 | 86 | 15.5 | 22.5

| (76-79) | (83-88) | (14.5-15.0) | (21.7-23.0)

----------------+---------+---------+-------------+-------------

_Specimens examined._--Total number, 18 (9 males, 9 females), as

follows: Palau Islands, USNM--Koror, 2 (Nov. 6, 18)--Babelthuap, 1

(Nov. 27)--Peleliu, 4 (Aug. 29, 30, 31); AMNH--exact locality not

given, 11 (Nov., Dec.).

_Molt._--Some of the birds taken in August are in molt. Specimens

taken in November and December are mostly in fresh plumage.

Apparently this bird molts in late summer and early fall.

_Remarks._--In 1945 the NAMRU2 party found the Palau Fantail in small

numbers at Peleliu, Garakayo and Ngabad. At Peleliu the birds were noted

as singles or in pairs in brushy undergrowth in forested areas. The

birds were observed also in the second growth vegetation in the battle

areas. Coultas (field notes) found the bird to be rare and restricted to

the true forest, when he visited the Palau Islands in 1931. The fantail

is one of the most attractive birds found in the jungles of the Palau

Islands. Its bright rufous coloring is conspicuously displayed by the

rapid movements of the wings and tail as the bird moves and feeds in the

undergrowth. The population is apparently not large, and the individual

or pair of birds probably ranges in a relatively large home territory.

_Evolutionary History of Rhipidura in Micronesia._--The evolutionary

history of _Rhipidura_ in Micronesia has been studied considerably more

than that of some of the other genera in the area. Oustalet (1896:70)

notes a close relation between _Rhipidura_ of the Marianas and _R.

rufifrons_ of Australia. Mayr (1941b:202, 203) regards the genus

_Rhipidura_ as typical of the Polynesian area and remarks that

speciation within this genus has proceeded at a relatively rapid rate.

Mayr and Moynihan (1946) have devoted a 21-page paper to a thorough

discussion of the _R. rufifrons_ group, based on the extensive

collections at the American Museum of Natural History. They remark that

no other genera are closely related to _Rhipidura_ and that evolution

has proceeded further in _R. rufifrons_ than in any other species of the

genus. These authors regard the Papuan area, probably New Guinea, as the

original home of this group. From their study they point out that many

of the subspecies of _R. rufifrons_ of the Papuan area, especially those

of the Louisiades and the Solomons, appear to be the least specialized

of the species, and that this lack of specialization in these subspecies

indicates that the ancestral stock of the species _R. rufifrons_

acquired its specificity somewhere in that area. With regard to the

kinds of _Rhipidura_ in Micronesia, Mayr and Moynihan (1946:fig. 2) have

logically found three separate colonizations within the area: one

represented today by _R. lepida_ at Palau; one of subspecies of _R.

rufifrons_ at Yap and in the Marianas; and one by _R. r. kubaryi_ at

Ponapé.

_R. lepida_, according to Mayr and Moynihan (1946), is a result of an

early colonization by _Rhipidura_. It is related to _R. dedemi_, _R.

superflua_, and _R. teijsmanni_, which are mostly monotypic or have only

two or three subspecies within the species. These three species are

found in the region including Celebes and the Moluccas. _R. lepida_

apparently invaded the Palau Islands from Celebes or an adjacent area

and, among named species, most closely resembles _R. teijsmanni_. Both

of these species have a white chin and throat, black breast patch, and

rufous abdomen. _R. lepida_ has become differentiated chiefly by the

presence of a rufous head and back, a more distinct breast band, and

proportionately different amounts of rufous and black coloration of the

tail feathers.

Mayr and Moynihan (1946:6) give as the chief characters of _R.

rufifrons_ the following: "a rufous forehead, a grayish brown head and

upper back, a well-defined rufous rump, a white chin and throat, a black

breast band with scaling at its lower edge, and a dark brown tail with a

distinct rufous base and a white tip." The Micronesian subspecies of _R.

rufifrons_ at Yap and in the Marianas display these characters. Of the

four subspecies found in the area including Yap and the Marianas, _R. r.

versicolor_, _R. r. saipanensis_, _R. r. mariae_ and _R. r. uraniae_,

the two first named most closely approach the ancestral stock, which may

have been _R. r. commoda_ Hartert of the northern Solomons or some near

relative in Melanesia. The amount of white on the chin and throat and on

the malar stripe, in _R. r. versicolor_ and _R. r. saipanensis_ is

probably nearer that which obtained in the ancestor. At Rota, _R. r.

mariae_, exhibits less white on the throat and a thinner, white malar

stripe, while at Guam, _R. r. uraniae_ possesses only a small amount of

white on the chin and only a very thin line of white in the malar

region. This variation in coloration suggests that the birds may have

originally become established at Yap, Saipan and Tinian and later, birds

from Saipan and Tinian spread to Rota and lastly to Guam.

_R. r. kubaryi_ of Ponapé, although considered as a subspecies of _R.

rufifrons_ by most workers, has lost the rufous coloring found in most

members of the species. Mayr and Moynihan (1946:6) point to its

evolution through subspecies in the Santa Cruz Islands, where in _R. r.

agilis_ Mayr the rufous of the lower back is restricted to the upper

tail-coverts, and in _R. r. melanolaema_ Sharpe and _R. r. utupuae_ Mayr

the rufous is absent. In the latter two subspecies, as well as in _R. r.

kubaryi_, the forehead is white instead of rufous.

The invasion of Micronesia by _Rhipidura_ has undoubtedly been the

result of abnormally long flights by a relatively weak flyer. The fact

that _Rhipidura_ has succeeded in establishing itself at only a few of

the seemingly suitable islands in Micronesia may indicate that the

possibilities for chance migration and resulting colonization are small,

but that new colonization may be expected in the future.

It is my opinion that the populations of _Rhipidura_, as I have observed

them in Micronesia, are small because each individual or pair of birds

is dependent on a relatively large area of woodland to satisfy its

habitat requirements, especially for food. This suggestion needs to be

tested by observation made in the field. In comparison with the insect

fauna of New Guinea or some other large island, that of Micronesia is

indeed small in number of kinds. Hesse, Allee and Schmidt (1937:524)

explain the absence of insectivorous animals such as "swallows, swifts,

flycatchers, and insectivorous bats" in island communities on the basis

of the small number of flying insects in these communities. Probably

_Rhipidura_ is able to forage for sedentary insect life as well as for

the flying forms.

=Metabolus rugensis= (Hombron and Jacquinot)

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