-- A new species of parakeet, Pyrrhura orcesi sp. nov., from southwestern Ecuador is described and named the E1 Oro Parakeet. This species is most closely related to the Maroon-tailed Parakeet (P. melanura). Pyrrhura orcesi is restricted to a narrow band of forest, between ca 600 to 1100 m in elevation, along the western slope of the Ecuadorian Andes. Its range is only ca 100 km in length, and, given the current rate of deforestation in the area, it soon may be threatened with extinction. Received 26 Mar. 1987, accepted 3 June 1987.
In August 1980 a field party consisting ofR. S. Ridgely, P. Greenfield,
and R. A. Rowlett was investigating remnant patches of cloud forest west
of Pitias, Prov. E10ro, Ecuador, at ca 900 m on the west slope of the
Andes. On 4 August, the group observed a flock of nine parrots, clearly
members of the genus Pyrrhura, landing in the canopy. The flock was
observed for about 15 min; all members of the flock displayed a red
forecrown and a virtual lack of breast scaling. No known member of the
genus shares such characters; however, no photographs or voucher spec-
imens were obtained.
Not until June 1985 could a return expedition be organized, under the
auspices of the Academy of Natural Sciences, Philadelphia (=ANSP) and
the Museo de Ciencias Naturales in Quito, Ecuador. Members of the
expedition spent three weeks during late June and early July in the region
of the original discovery, found the parakeet to be relatively numerous
in what forest habitat remained, and collected 12 specimens. In August
Dept. of Ornithology, Academy of Natural Sciences, Philadelphia, 19th and The Parkway, Philadelphia,
Pennsylvania 19103.
173
174 THE WILSON BULLETIN Vol. 100, No. 2, June 1988
1986, a field party returned to southwestern Ecuador to determine the
northern limit of the bird's distribution, and obtained four additional
specimens at a site ca 100 km north of the original locality. In addition,
a heretofore unrecognized specimen of the bird in the British Museum of
Natural History, Tring (=BM) was brought to our attention by T. Schu-
lenberg. Study of this material, and of specimens of related species in the
genus Pyrrhura, convinces us that the new parakeet deserves recognition
as a full species, which we propose to name:
Pyrrhura orcesi sp. nov.
EL ORO PARAKEET
HOLOTYPE.--Academy of Natural Sciences No. 177523; adult male, ca 9.5 road km
W of Pitias, ca 900 m, 3 40'S, 7944'W, Prov. E10ro, Ecuador, 21 June 1985; collected by
Mark B. Robbins, original number 1541.
DIAGNOSIS.--A Pyrrhura parakeet most similar to P. melanura. Readily distinguished
from all forms of that species by its obsolete scaling on the breast and sides of neck, its red
frontal band, and its much greener crown (the feathers without any dusky-brown centers).
Superficially resembles geographically distant P. rhodocephala, but differs strikingly in its
smaller size, having only forecrown red (not the entire crown), green (not red) ear-coverts,
red (not white) alula and median coverts, and much more green in tail.
DISTRIBUTION.--So far, known only from three localities, all on the west slope of the
Andes of southwestern Ecuador in Provs. E10ro (the type locality and Piedras) and Azuay
(7 km E of Naranjal, 2 40'S, 7932'W), at elevations ranging from 600 to 1100 m. Presumably
occurs in intervening areas at appropriate elevations, and where suitable forest remains
(Fig. 1).
DESCRIPTION OF HOLOTYPE.--General coloration green, closest to Parrot Green
(Color 60; capitalized colors from Smithe 1975, 1981), but shinier and brighter than that
color on face, crown, nape, back, rump, and abdomen; slightly darker and duller on the
wing-coverts and breast. Pale buffy grayish marginations virtually absent from breast feath-
ers, but somewhat more pronounced on sides of neck. Center of abdomen with slight maroon-
red suffusion. Broad (ca 5 mm) frontal band Geranium (Color 12), extending back to just
in front of eye. Outermost greater and median primary coverts, as well as the alula, Geranium
Pink (Color 13), somewhat more intense on bend of wing. Outer webs of outer primaries
blue, very narrowly edged with green. Tail above mostly Burnt Sienna (Color 132), with
outer webs and base green; below mostly dusky with inner webs margined with Burnt Sienna.
Soft part colors in life: irides dark brown; tarsi black; bill horn; eye ring pinkish-white.
MEASUREMENTS (mm).--Wing (chord) 123.2; tail 102.2; culmen from anterior edge
of cere 16.4; mass 73 g.
SPECIMENS EXAMINED.--Pyrrhura orcesi: ECUADOR: type locality 11 (ANSP), 1
skeleton (photo of fresh skin in VIREO VO1-3-007-011); Prov. E10ro, Piedras, 1 (BM);
Prov. Azuay, Naranjal, 3 (ANSP), 1 (Museo Ecuatoriano de Ciencias Naturales, Quito). P.
m. pacifica: ECUADOR: Prov. Esmeraldas, San Lorenzo, 5 (ANSP), San Mateo, 1 ([FMNH=]
Field Museum of Nat. Hist.), Lita, 1 ([AMNH=] American Museum of Nat. Hist.); Prov.
Pichincha, Rio Blanco, 1 (ANSP); P.m. melanura: VENEZUELA: Amazonas, Cerro Duida,
7 ([MCZ=] Museum of Comparative Zoology, Harvard), Boca de Sina, 1 (MCZ), E1 Mercy,
3 (MCZ); BRAZIL: Amazonas, Iauarete, 1 (MCZ), Tahuapunto, 2 (MCZ), Lago Tefe, 1
(MCZ), Rio Mirapinimi, 1 (MCZ), Rio Mazan, 1 (MCZ); ECUADOR: Prov. Pastaza, Chi-
cherota, 1 (ANSP), Montalbo, 2 (ANSP); Prov. Napo, Limnoncocha, 1 ([LSUMZ=] Loui-
Ridgely and Robbins o NEW PARAKEET FROM ECUADOR 175
FIG. 1.
Type locality of the El Oro Parakeet.
siana State Univ. Museum of Zoology, Baton Rouge), Archidona, 1 (AMNH); Prov. Morona-
Santiago, Huila, [incorrect locality]; PERU: Dept. Loreto, Rio Curaray, 2 (MCZ), 80-90 km
N of Iquitos, 7 (LSUMZ), Rio Nanay, 2 (FMNH), Apayacu, I (ANSP), Morado-Pamba, 2
(FMNH); P.m. souancei: ECUADOR: type, no locality, I (BM); COLOMBIA: Dept. Ca-
quetfi, Morelia, 5 (ANSP); Dept. Putumayo, Umbria, I (ANSP), Puerto Asis, I (ANSP),
San Antonio, I (FMNH); Dept. Meta, La Macarena, I (FMNH); P.m. berlepschi: PERU:
Dept. San Martin, Nuevo Loreto, 2 (AMNH), Tarapota, I (LSUMZ); ECUADOR: Prov.
Morona-Santiago, Cord. de Cutucfi, 1 (ANSP), Macas, I (AMNH), I (photograph, VIREO,
RI0-1-005); Prov. Pastaza, Rio Curaray, I [incorrect locality]); P.m. chapmani: COLOM-
BIA: Dept. Huila, La Plata (type locality), 4 (ANSP), La Candela, 3 (ANSP), E1 Isno, 4
(ANSP), San Agustin, 2 (ANSP); Dept. Cauca, Moscopfin, 2 (ANSP), 3 (FMNH); P. rho-
docephala: VENEZUELA: M6rida, E1 Valle, I (ANSP).
ETYMOLOGY. -- We are pleased to name this species in honor of Dr. Gustavo Orc6s
V., in recognition of his many contributions to Ecuadorian ornithology and his continuing
encouragement of younger generations of field biologists. The proposed English name, E1
Oro Parakeet, refers to the province in Ecuador where this species was discovered.
REMARKS
Variation within the species.--Only very slight variation is apparent
within adults ofP. orcesi. Besides the holotype, only four other individuals
(ANSP 177524, 177522, 177525, 177528) show even a hint of red on the
176 THE WILSON BULLETIN Vol. I00, No. 2, June 1988
center of the abdomen; in all other examples, the abdomen is more or
less uniform green. However, young birds (based on presence of bursa
Fabficius in some individuals, and on begging behavior in others; ANSP
177526, 177530, 178081, 178083, plus 177533, which was preserved as
a skeleton, but photographed before preparation; VIREO VO1-3-007-
011) show markedly reduced red on the frontal area and have the red on
the wing entirely or virtually restricted to the carpal edge (there is con-
siderable variation, presumably due to molt stage). On one specimen
(ANSP 177524), the entire 9th primary on the fight wing is red.
Systematic relationships.--The closest relative ofP. orcesi is the rather
variable species P. melanura. The two species share relatively small size
and overall plumage pattern, including tail and wing pattern and color.
All races of P. melanura, however, show conspicuous narrow to broad
pale tipping on the breast feathers and sides of neck, absent (or virtually
so) in P. orcesi (see Fig. 2). All races ofP. melanura do show a faint trace
of reddish on the feathers just above the maxilla, most marked in P.m.
pacifica, the race of melanura found on the western slope to the north of
the range ofP. orcesi (Fig. 2). This hint of color could argue for considering
orcesi as merely the southwestern Ecuador representative ofP. melanura.
However, in none of the six available specimens of pacifica does this in
any way approach the condition found even in young P. orcesi (in which
the amount of red on the forecrown is reduced); furthermore, the color
itself differs, being (in pacifica) closest to Brick Red (Color 132 A). In
addition, while we are uncertain whether this has any taxonomic signif-
icance, the eye ring of pacifica is gray (Arndt 1983, pers. obs.), while that
ofP. orcesi is pinkish-white.
During the course of assessing the relationship of P. orcesi to the P.
melanura complex, we critically examined specimens of melanura in
American museums, and a number of problems came to light. Five sub-
species ofP. melanura have been described. Nominate, souancei, berlep-
schi, pacifica, and chapmani are known from various parts of western
Amazonia or from the slopes of the northern Andes. Both chapmani and
pacifica are isolated geographically and are relatively well differentiated.
Chapmani differs from all other forms of P. melanura by virtue of its
larger size in all measurements (see Table 1). It further differs in occupying
a higher elevation zone than other races, ca 1600-2800 m (Forshaw and
Cooper 1973); the lowest point at which it has been recorded is thus above
the highest known elevation (1500 m, berlepschi,' VIREO R10-1-005) for
FIG. 2. The Pyrrhura melanura superspecies complex. Clockwise from lower left: P.
orcesi, range = red; P.m. pacifica, range = diagonal lines; P.m. chapmani, range = stippled;
P.m. melanura/souancei, range = light gray; P.m. berlepschi, range = black. Thin red line
represents 1000 m contour. Painting by Paul Greenfield.
Ridgely and Robbins NEW PARAKEET FROM ECUADOR 177
TABLE 1
SELECTED MEASUREMENTS (MM) OF THE PYRRHURA MELANURA
SUPERSPECIES COMPLEX
Wing chord Tail length Mass
Species N Range (mean) N Range (mean) N Range (mean)
Orcesi 15 113.8-127.7 11 90.0-103.1
(119.2) (98.2)
Melanura pacifica 6 118.8-129.0 6 90.0-99.6
(124.3) (92.9)
M. melanura 21 119.6-133.9 19 101.6-120.0
(126.6) (109.9)
M. souancei 9 121.0-129.6 8 102.7-112.5
(127.9) (112.5)
M. chapmani 16 133.0-141.8 13 118.1-132.6
(136.8) (125.2)
14 65.0-73.5
(70.8)
9 64.0-79.0
(73.3)
any other form in the species. It might, in fact, be argued that chapmani
deserves to be recognized as a full species (as indeed it was described;
Bond and Meyer de Schauensee 1940), but we hesitate to do so in the
absence of supporting evidence from other lines of investigation (e.g.,
biochemical).
Pyrrhura m. pacifica is also geographically isolated from other forms
ofP. melanura, being the only race found on the west slope of the Andes.
It differs most obviously in its shorter tail (Table 1) and grayish eye ring
(whitish to white in all other races of P. melanura; Arndt 1983, pers.
obs.); in other respects it most resembles representatives of the species
found far to the east in Amazonia, i.e., it has narrower breast scaling.
What is now known as P.m. melanura was described by Spix (1824)
on the basis of two specimens taken at Tabatinga, a town in what is now
Amazonas, Brazil, on the north bank of the Amazon near Leticia, Co-
lombia. P.m. souancei was described as a species by Verreaux (1858) on
the basis of three specimens to which he ascribed no locality, and with
no reference to the description of the very similar melanura; none of the
three specimens was designated as the holotype. Both descriptions of
melanura and souancei, were accompanied by plates, rather crudely ren-
dered; the birds depicted appear very similar. Sclater (1862) restricted the
type locality of souancei, with no explanation, to "Rio Napo." We pre-
sume that Sclater had access to information, not available now, when he
did so. In fact, the one specimen of the three syntypes that we have
examined (BM 59.11.22.25) is marked "Rio Negro." The two forms were
first considered conspecific by Chapman (1926), who correctly established
178 THE WILSON BULLETIN VoL 100, No. 2, June 1988
that souancei resembled nominate melanura but for its relatively wider
pale breast scaling. Neither Chapman nor Peters (1937), however, seems
to have addressed adequately the problem of souancei's actual range,
Peters listed it as "Amazonian Ecuador" (which at that time extended
east to the Iquitos area in what is now northeastern Peru). Following this,
specimens of this parakeet from anywhere in or near the Napo drainage
have usually been labeled souancei.
Based on the available series of specimens from numerous localities,
we believe that this is not the best treatment. Birds from the middle and
lower Napo drainage, in fact, closely resemble birds from southern Ven-
ezuela and northwestern Brazil, nominate melanura: they have narrow
breast scaling. Not until one gets relatively close to the Andes, or ascends
their lower slopes, does one consistently find birds with relatively broader
breast scaling. It is to this population that the name souancei should be
applied; thus we restrict the type locality of souancei to the "upper Rio
Napo." We should point out that gene flow apparently occurs between
these two forms.
These broad-scaled birds also appear to exhibit geographic variation.
Several birds of a small series (N = 9) from western Caquetfi and western
Putumayo in southeastern Colombia seem virtually identical with the
type of souancei. Southward along the base of the Andes, however, there
occurs another population of birds with even broader, and consistently
whiter foreneck scaling. This population was described by Salvadori (1891)
as P. berlepschi, with the type locality of Chyavetas (=Chayahuitas, Dept.
Loreto) in northeastern Peru south of the Rio Marafi6n. Still known from
very limited Peruvian material, we believe that a recent specimen (ANSP
176701) taken on the western slope of the Cordillera de Cutucfi in south-
eastern Ecuador, as well as a photograph of a netted bird from the nearby
Upano River valley (VIREO R10-1-005) are referable to berlepschL ex-
tending the range of this form ca 320 km northward. It should be noted
that in the Colombian series there is also at least one bird (FMNH 286758)
that approaches typical berlepschi in the width of its breast scaling. No
such variation is apparent in the series of berlepschi from Peru and south-
ern Ecuador available to us (5 of the 6 known specimens), but this may
simply reflect inadequate material of berlepschi. Should variation in ber-
lepschi prove to be comparable to that seen in souancei, we would syn-
onymize berlepschi with souancei.
Two anomalous specimens deserve mention. One, AMNH 230883,
taken by the Olalla brothers, is labeled as having been collected at "Boca
Rio Curaray," well within the range of nominate melanura (as defined
above). Two other typical melanura (MCZ 137818, 137817) were ob-
tained there on virtually the same date, but this particular specimen seems
in every way identical to berlepschi. We suspect the locality is inaccurate.
Ridgely and Robbins NEW PARAKEET FROM ECUADOR 179
Another specimen (AMNH 156769), is labeled as having been obtained
at "Huilca" in Ecuador. The precise location of this town seems uncertain
(see Paynter and Traylor 1977), but is seems unlikely to be in the "Macas
Region," as its tag is labeled, and the bird appears to be referable to
nominate melanura. The latter may have been a cagebird (its rectrices
are very heavily worn), perhaps transported over the Cordillera de Cutucfi
from east of the Andes (as RSR has observed local Shuar Indians doing
with Pionites melanocephala and other parrots).
To summarize, we would recommend considering birds from virtually
the entire Amazon basin as P.m. melanura, restricting P.m. souancei to
a limited area near the base of the Andes in southeastern Colombia (and
probably adjacent northeastern Ecuador), and P.m. berlepschi to a rela-
tively small area on the east slope of the Andes in northeastern Peru and
southeastern Ecuador. The extent of gene flow between souancei-berlep-
schi and nominate melanura presumably is unimpeded, although to date
there is no specimen material conclusively demonstrating this. Likewise
there is presumably a connection between souancei and berlepschi along
the east slope of the Andes, also as yet not found; they may prove to be
the same group.
A problem that needs to be addressed is the possible relationship of P.
melanura and P. albipectus. This question came to light during our in-
vestigations in 1984 on the Cordillera de Cutucfi in southeastern Ecuador,
when we found a somewhat variable population of P.m. berlepschi on
the lowermost slopes of the cordillera. One specimen was taken, and a
significant amount of white on the breast of flock members was observed,
with some showing almost all white. At higher elevations, what appeared
to be pure flocks of P. albipectus were found; two specimens were taken.
One interpetation of this distribution would be to consider albipectus as
a partially localized upper-elevation replacement of P.m. berlepschi, but
we hesitate to do this because of complications elsewhere (Robbins et al.
1987).
Distribution, habitat, and ecology.--The known range of this species is
no more than 100 km in length and between 5 and 10 km in width,
extending north from the type locality (Fig. 1) to just east of Naranjal,
Prov. Azuay. Despite extensive searches, we failed to find orcesi north of
the Naranjal site, and, in fact, no Pyrrhura was found at the appropriate
elevations in the provinces of Cafiar or Bolivar. Pyrrhurra melanura pa-
cifica is unrecorded south of Rio Palenque, Prov. Los Rios, ca 280 km
north of the northernmost locality of orcesi. It thus appears that a gap
exists between the ranges of orcesi and m. pacifica. Within this gap, at
elevations where orcesi and m. pacifica should occur, a substantial amount
of naturally occurring vegetation has been converted to orange groves and
other agricultural use. Nevertheless, it appears that this gap may not have
180 THE WILSON BULLETIN Vol. 100, No. 2, June 1988
been artificially induced, as a number of early collectors (e.g., Rhoads in
1911; Gill in 1921; Chapman et al. in 1922; see Bucay locality in Paynter
and Traylor 1977) spent considerable time at appropriate elevations in
this region without obtaining Pyrrhura.
We found P. orcesi only in a narrow band of humid, upper tropical
zone forest, between 600 and 1100 m. The British Museum specimen
(53.68.106), which L. Gomez collected at Piedras, however, is noted as
having been obtained at 300 m. Perhaps at the time this specimen was
taken (9 September 1939), suitable cloud forest extended lower than it
does anywhere at present; Gomez obtained only one specimen, so perhaps
the species was rare at that locality. At the type locality, forest canopy
height on the more level areas exceeded 20 m, although average canopy
height was lower on steeper slopes. During our investigation, the forest
usually was enshrouded by clouds from predawn until about midday
(VIREO RO8-7-014). Trees and the relatively dense understory were
laden with epiphytes. Moisture is carried by westerly winds from the
Pacific Ocean (ca 75 km west of the type locality). The forest at the
Naranjal site was very similar to the E10ro site, except that it was even
more fragmented by human activity.
At the E1 Oro site, at least six flocks of birds, comprised of from four
to twelve individuals per flock, were observed. A highly conservative
count gave us a total of between 55-60 birds at the type locality. Over
twenty, in three different flocks, were recorded at the Naranjal locality.
Flocks consisted of adults and young of both sexes. On 27 June 1985 in
the early morning, Robbins observed a flock of four individuals foraging
on fruit in the canopy of a tall tree. One of the individuals, a bird with
no apparent red forecrown, was giving a distinctive, slightly higher-pitched,
more raspy, and shorter call than the flight and contact calls of the birds
it was with. As it called, its head, body, and tail were oriented horizontally,
with its wings extended and constantly quivering. This behavior was di-
rected at a nearby bird which had a broad red forecrown. On four separate
instances the "red-fronted" individual regurgitated food to this bird. At-
tempts to collect the begging individual failed. At 12:00 on the same day,
Robbins again encountered what appeared to be the same flock. Begging
by a single individual was again observed. This bird (ANSP 177526)
proved to be a female, in fresh plumage, with only a hint of a red fore-
crown. The throat and crop were filled with regurgitated fruit. The pre-
vious day another collected individual (ANSP 177533; VIREO VO 1-3-
007-011) with little red on forecrown, in fresh plumage, also had its throat
and crop filled with regurgitated fruit. Both of these birds had less red in
the alula and the outermost greater wing coverts than birds that had
relatively broad red frontal bands.
Ridgely and Robbins NEW PARAKEET FROM ECUADOR 18 1
Further evidence that birds with a reduced amount of red in the fore-
crown and on the bend in the wing are immatures comes from birds
collected in 1986 at the Naranjal site. Two of the four birds collected
(ANSP 178081, 178083) had the bursa present, and both of these birds
had minimal amounts of red in the forecrown and the alula and outermost
greater wing coverts. The other two birds that had larger amounts of red
in the above regions did not have the bursa. Our 1985 series ofparakeets
unfortunately were not examined for the presence of bursa. No difference
in soft part colors were noted between adults and immatures. Given that
some young birds were begging food in late June, we speculate that the
main breeding period for orcesi is from March through May.
At the type locality, the birds were observed feeding repeatedly at a fig
(Ficus cf. macbridei; section Pharmacosycea) and on the fruit of Helio-
carpus popayanensis (family Tiliaceae). At the Naranjal site, the parakeets
were observed feeding only on the fruit of Hieronyma sp. (family Eu-
phorbiaceae).
Conservation.--The natural forest habitat at the type locality and the
Naranjal site has been reduced significantly by human activity (VIREO
RO8-7-004, 006-009, 011,018-024). At the E10ro site, between 10 and
15 large trees were being removed daily from a small tract of accessible
forest (see Fig. 1); typically, once the larger trees are removed, the area
is burned and cattle are brought in. Although orcesi was relatively nu-
merous and appeared to be thriving in the patchy forest now found at
both localities, significant further disturbance and fragmentation of the
forest may eliminate vital nesting and feeding sites. Fortunately, there is
still extensive, mostly inaccessible forest remaining between the type lo-
cality and the Naranjal site. We strongly recommend that a sizable tract
of land in this area be preserved, not only to insure that a large population
of the parakeet is protected, but also to protect other taxa that have
distributions restricted to this region (e.g., the Ochre-bellied Dove [Lep-
totila ochraceiventris]).
ACKNOWLEDGMENTS
We are extremely grateful to the Museo Ecuatoriano de Ciencias Naturales, Quito, es-
pecially Dr. F. Sarmiento and J. C. Matheus, for their invaluable help with planning and
logistics of our 1985 and 1986 expeditions, as well as for field assistance. The Ministerio
de Agricultura, Quito, provided permits. We are indebted to W. T. Cooper for his painting
of the new parakeet. P. Greenfield kindly provided the painting of the new species and its
relatives, as well as helping in Quito and in the field. T. Pedersen provided artistic advice.
We thank K. Berlin for providing financial and field assistance on the first expedition, while
the RARE Center for Tropical Bird Conservation provided financial support for further
assessing the status and distribution of the new parakeet in 1986. B. Stone (ANSP), C. Berg
(Norwegian Arboretum and Botanical Garden, Univ. of Bergen, Norway), J. Kallunki (New
182 THE WILSON BULLETIN VoL 100, No. 2, June 1988
York Botanical Garden), the Aarhus Univ. Herbarium, Denmark, kindly identified botanical
specimens. We are grateful to T. S. Schulenberg for bringing to our attention the presence
of the Tring specimen of what proved to be the new parakeet. We are also grateful to M.
Dolack for translating several articles. We thank the following people and institutions for
the loan of their valuable specimens: M. LeCroy, American Museum of Natural History; J.
Fitzpatrick and D. Willard, Field Museum of Natural History; J. V. Remsen, Jr. and S.
Cardiff, Louisiana State Museum of Zoology; and R. Paynter, Jr., Museum of Comparative
Zoology; and we also thank G. Cowles, of the British Museum, Tring for photographing the
three types (and daring to send us one!) ofsouancei. We thank K. Bildstein, G. Graves, and
K. Parkes for comments on the manuscript.
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Neptune City, New Jersey.
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CH^'Ma, F.M. 1926. The distribution of bird-life in Ecuador. Bull. Am. Mus. Nat. Hist.
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FORSH^W, J. M. ^rD W. T. COO'R. 1973. Parrots of the world. Lansdowne Press, Mel-
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P^YNTER, R. A., JR. tqD M. A. T3/4IOR, JR. 1977. Ornithological gazetteer of Ecuador.
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Museum, Vol. XX. Taylor and Francis, London, England.
SCL^XER, P.L. 1862. Catalogue of a collection of American birds. N. Trubner and Co.,
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SMITHE, F.a. 1975. Naturalist's color guide. Am. Mus. Nat. Hist., New York, New York.
1981. Naturalist's color guide, Part III. Am. Must. Nat. Hist., New York, New
York.
SeIx, J.B. 1824. Avium Brasiliam. F. S. Hubschmann, Munich, West Germany.
VeRRUX, J. 1858. Description d'un perroquet nouveau. Rev. et Mag. de Zoologie. 10:
437-438.