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South American Journal of Herpetology, 4(1), 2009, 9-16

2009 Brazilian Society of Herpetology

A new species of Scinax (Anura: Hylidae) from


the area of Iquitos, Amazonian Peru
Ji Moravec1,5, Illich Arista Tuanama2, Pedro E. Prez3, and Edgar Lehr4
1
Department of Zoology, National museum, 115 79 Praha 1, Czech Republic.
2 Urb. Sgto. Lores F 6, Iquitos, Peru.
3
Las Palmeras 324, Iquitos, Peru.
4 Natural History State Collection, Koenigsbruecker Landstrasse 159, 01109 Dresden, Germany.
5
Corresponding author: jiri.moravec@nm.cz

Abstract. We describe a new species of the hylid frog genus Scinax from the Peruvian Upper Amazonian Lowlands (area of
Iquitos, Region Loreto, Peru). The new species belongs to the Scinax ruber clade and differs from all its members by having the
dorsal skin slightly to coarsely shagreen, by lacking conspicuous ulnar and tarsal tubercles, and in life by having a distinct light
olive-green coloration on dorsum, bright yellow flanks with distinct black spots, black posterior surfaces of thighs, and gold to
bronze iris.

Keywords. Anura, Hylidae, Scinax iquitorum new species, Amazonia, Peru.

Introduction of Scinax different from all other Upper Amazonian


species was discovered. It is herein described as a
Currently the hylid frog genus Scinax comprises new species.
95 recognized species and represents the second rich-
est genus of the subfamily Hylinae (Frost, 2008).
Altogether eight species of Scinax are listed from Materials and Methods
the Ecuadorian and Peruvian Amazonia (Duellman
and Wiens, 1992, 1993): S.chiquitanus (De la Riva, The type series comprises one subadult and three
1990), S.cruentommus (Duellman, 1972), S.funere- adult specimens. Sex was determined by presence or
us (Cope, 1874), S.garbei (Miranda-Ribeiro, 1926), absence of secondary sexual characters (vocal sac,
S.ictericus Duellman and Wiens, 1993, S.oreites vocal slits) or by direct observation of the gonads.
Duellman and Wiens, 1993, S.pedromedinae (Henle, All measurements and terminology follow Duellman
1991), and S.rubber (Laurenti, 1768). Another five (1970, 2001). Snout-vent length (SVL) was mea-
species have been reported from the adjacent Amazo- sured to the nearest 0.5mm and other measurements
nia of Bolivia, Brazil, Colombia, and Venezuela (De to the nearest 0.1mm with calipers. When structures
la Riva etal., 2000; Duellman, 1972; Goin, 1966; were smaller than 5mm, measurements were taken
Lutz, 1973; Pyburn, 1992; Rivero, 1961): S.baum- with an ocular micrometer attached to a Leica MS
gardneri (Rivero, 1961), S.boesemani (Goin, 1966), 5 stereomicroscope. Webbing formulae follow Sav-
S.fuscomarginatus (Lutz, 1925), S.lindsayi Pyburn, age and Heyer (1967) as modified by Myers and
1992, and S.nebulosus (Spix, 1824). Traditionally, Duellman (1982) and Savage and Heyer (1997).
these species have been arranged in the species groups Color in life was described based on field notes and
of S.ruber, S.rostratus (Peters, 1863), S.staufferi color photographs of live specimens. Drawings were
(Cope, 1865), and Scinax x-signatus (Spix, 1824) made by using a stereomicroscope with drawing tube
(e.g. Duellman and Wiens, 1992, 1993; Pombal etal., attachment.
1995). However, according to Faivovich (2002), it Museum abbreviations are as follows: AMNH
appears to be more appropriate to include all the men- American Museum of Natural History, New York,
tioned species in the more inclusive S.ruber clade. U.S.A.; GNM Gteborg Natural History Museum,
In the framework of a scientific cooperation be- Sweden; KU Natural History Museum of Kansas,
tween the National Museum, Prague, Czech Repub- Lawrence; MUSM Museo de Historia Natural,
lic, and the Universidad Nacional de la Amazona Universidad Nacional Mayor de San Markos, Lima,
Peruana, Iquitos, Peru, two of the authors (J.M. and Peru; NMP6V and NMP6F: National Museum (Natu-
I.A.T.) conducted two short-term surveys of herpeto- ral History), Prague, Czech Republic; ZFMK Zool-
faunal diversity in the surroundings of Iquitos in 2001 ogisches Forschungsinstitut und Museum Alexander
(Moravec etal., 2002 a, b). At this occasion a species Koenig, Bonn, Germany.
10 New species of Scinax

Results can be detected in proximal outer edge of tarsus);


(4)tubercles absent on heel; (5)tubercles absent on
Scinax iquitorum sp.nov. (Figs.13) lower jaw; (6)skin on dorsum slightly to coarsely

Holotype MUSM 27577, adult female from the vicin-


ity of Puerto Almendras (034946S, 0732232W;
ca.120m a.s.l.,), ca.17km straight SW of Iquitos,
Region Loreto, Peru, collected by J. Moravec on 8
April 2002.

Paratypes NMP6V 71267/13, one adult male, one


adult female, and one subadult, collected at the type
locality by J. Moravec on 89 April 2002.

Referred material (photo vouchers) Adult female


(photo numbers NMP6F 12) from middle stream
of Rio Nanay, 033149S, 0742525W, collected
by Pedro E. Prez on date; adult female (photo num-
ber NMP6F 36), area of Rio Yavari, 043931S,
0720246W, collected by Pedro E. Prez.

Diagnosis A moderate-sized species of the ge-


nus Scinax (webbing between toes I and II does not
extend beyond the subarticular tubercule of toe I)
belonging to the Scinax ruber clade (sensu Faivov-
ich, 2002) characterized by the following combina-
tion of characters: (1)male SVL 35.0mm, females
38.5mm; (2)snout rounded, not acuminate, in dor- Figure1. (A)Head, (B)hand, and (C)foot of Scinax iquitorum
sal and lateral views; (3)ulnar and tarsal tubercles sp.n. (holotype MUSM 27577, female; SVL 38.5). Scale bar
indistinct (inconspicuous traces of small tubercles equals 5mm.

Figure2. Variation in dorsal color pattern of Scinax iquitorum sp.n.: holotype (left) and paratypes (NMP6V 71267/2,1,3). Scale bar equals
10mm.
Moravec, J. etal. 11

shagreen; (7)in life, dorsum light olive-green to (chlorine green in life); from S.boesemani in hav-
brown; (8)in life, flanks bright yellow with distinct ing black spots on dorsum and flanks (canthal and
round black spots becoming gradually larger from post-ocular dark stripes only) and in the black pos-
axillae to groin; (9)in life, concealed surfaces of legs terior surfaces of thighs (without pattern and paler
black; (10)in life, iris gold to bronze with irregular than the dorsum); from S.chiquitanus by the yellow
dark reticulation. flanks with black round spots (tan with or without
small dark spots) and the black posterior surfaces of
Comparison with other species Scinax iquitorum thighs (uniform tan, with or without a broad, dark
can be distinguished from all the species known from brown longitudinal stripe or lightly pigmented spots);
Upper Amazonian Lowlands by the following charac- from S.cruentommus (Fig.6) in lacking a horizon-
ter states (states in other species are described in pa- tal red streak through the eye, by the yellow flanks
rentheses according to Cope, 1870, 1874; Boulenger, with black round spots (pale with or without small
1882; Donoso-Barros, 1965 1964; Duellman, 1971, dark spots), and the black posterior surfaces of thighs
1972; Duellman and Wiens, 1993; De la Riva, 1990; (tan with diffuse covering of dark brown pigment);
Goin, 1966; Melin, 1941; Peters, 1863; Pyburn, 1992; from S.fuscomarginatus by the more robust body
Rivero, 1961; Spix, 1824; Werner, 1899). (slender) and presence of black spots on dorsum and
The nonacuminate snout, the absence of tubercles flanks (canthal and dorsolateral dark stripes only);
on head, dorsum, heels, and lower jaw, and the ab- from S.ictericus in lacking conspicuous ulnar and
sence of conical ulnar and tarsal tubercles differentiate tarsal tubercles, in the absence of small tubercles in
it from S.garbei, S.nebulosus, and S.pedromedinae. the supratympanic region, by the yellow flanks with
It differs from S.funereus (Fig.4) by its slightly black round spots (creamy white usually with small
to coarsely shagreen skin on the dorsum and legs (tu- round black or dark brown spots), and in the absence
berculate), by the absence of a conspicuous pattern of transverse bars on limbs; from S.lindsayi by the
of dark brown spots and elongate marks on dorsum more robust body (slender) and lack of canthal stripe
and transverse bars on limbs, by the yellow flanks and dark brown bars on limbs.
with black spots (yellow with dark brown stripes
or series of dashes), and black posterior surfaces of Description of holotype Adult female, body mod-
thighs (yellow with dark pigmentation concentrated erately slender; head narrower than body; head width
into dark brown spots or longitudinal stripes or pale 33.2% of SVL; head length 32.5% of SVL; head
with discrete dark blotches). slightly wider than long; snout bluntly rounded in
From S.oreites it differs by the absence of creamy dorsal and lateral views (Fig.1); eye-nostril distance
white dorsolateral stripes, by having yellow flanks equal to eye diameter; nostril slightly protuberant,
with black round spots (tan or brown) and black pos- its anterior margin at the same level of the anterior
terior surfaces of thighs (brown with yellow blotch margin of lower jaw; internarial region moderately
distally). depressed; canthus rostralis rounded; loreal region
It differs from S.ruber (Fig.5) by the lack of tan slightly concave; top of head flat; interorbital dis-
to yellow dorsolateral stripes, by having yellow flanks tance wider than upper eyelid width, 33.6% of head
with black round spots (cream with yellow spots usu- width; eye diameter 32.0% of head width; supratym-
ally edged with black in the groin) and by the black panic fold weakly marked; tympanum distinct, round,
posterior surfaces of thighs (brown with yellow to or- slightly wider horizontally; tympanum diameter
ange mottling enclosed in darker pigment). 56.1% of eye diameter.
Scinax iquitorum is larger than S.baumgardneri Axillary membrane absent; pectoral fold barely
(male holotype, 29.0mm), S.boesemani (maximum visible. Ulnar tubercles absent; fingers moderately
SVL in males 32.1mm), S.chiquitanus (maximum long, bearing relatively large elliptical discs and nar-
SVL in males 33.3mm and in females 36.2mm), row lateral fringes; palmar tubercle flat, bifid; thenar
S.cruentommus (maximum SVL in males 27.1mm tubercle slightly protruding, elliptical, with two and
and in females 30.6mm), S.fuscomarginatus (maxi- half to three times the size of subarticular tubercles;
mum SVL in males 22.4mm; Faivovich, unpublished subarticular tubercle of finger I subconical, as wide as
data), S.ictericus (maximum SVL in males 31.6mm the digit, proximally followed by a distinct smaller tu-
and in females 33.5mm) and S.lindsayi (maximum bercle; tubercles of fingers IIIV rounded, protruding,
SVL in females 27.7mm). Furthermore, S.iquitorum as wide as digits, being the distal tubercle of finger
differs from S.baumgardneri in its dorsal coloration IV more developed than the others; supernumerary
12 New species of Scinax

Figure4. Scinax funereus (KU221960b, female), from San


Figure3. Male paratype NMP6V 71267/1 of Scinax iquitorum Jacinto, Region Loreto, Peru. Photograph by W. E. Duellman.
sp.n. in life from Puerto Almendras, Region Loreto, Peru.
Photograph by J. Moravec.

Figure6. Scinax cruentommus (KU221958, unsexed), Teniente


Lopez, Region Loreto, Peru. Photograph by W. E. Duellman.

Figure5. Scinax ruber (NMP6V 71152, male), from Puerto


Almendras, Region Loreto, Peru. Photograph by J. Moravec.
smooth; skin on belly and ventral surfaces of thighs
granular; tongue ovoid; transverse vomerine dentig-
erous processes between ovoid choanae, narrowly
tubercles barely evident; all fingers basally webbed separated medially, bearing 7/6 teeth (left/right).
(Fig.1). Measurements (inmm): SVL 38.5; tibia length
Hind limbs moderately long; heels of adpressed 18.7; foot length 14.6; head length 12.5; head width
hindlimbs markedly overlap each other; tibiotarsal 12.8; internarial distance 3.0; interorbital distance
articulation extending approximately to the ante- 4.3; width of upper eyelid width 3.1; eye diameter
rior edge of eye; tarsal fold absent; tarsal tubercles 4.1; tympanum diameter 2.3.
inconspicuous (very small tubercles can be detected
on proximal outer edge of tarsus); tibia length 48.6% Color in life Dorsum light olive-green to brown;
of SVL; foot length 37.9% of SVL; inner metatarsal dorsal pattern consisting of small round dark dots ran-
tubercle low, flat, elliptical; outer metatarsal tubercle domly distributed on head and concentrated mostly
small, round; toes bearing elliptical discs, about as in areas of inconspicuous darker interorbital, scapular
large as those of fingers; subarticular tubercles round, and sacral transverse blotches; similar dots on lips;
protruding, as wide as digits, larger than those on fin- flanks bright yellow with very distinct black round
gers; supernumerary tubercles barely evident; web- spots gradually larger from axillae to groin; anteri-
bing on toes I22II12III12+IV21V (Fig.1). Skin or surfaces of thighs and concealed surfaces of legs
on dorsum slightly shagreen; skin on throat and chest black; ventral surfaces white; a row of black round
Moravec, J. etal. 13

spots on the anterior ventral side of the thighs; plan-


tar surfaces grayish; iris gold to bronze with irregular
dark reticulation; long bones of hindlimbs green.

Coloration in preservative Dorsum gray to brown


with inconspicuous darker interorbital, scapular and
sacral transverse blotches; flanks and ventral surfaces
white; dots and spots on dorsum and flanks dark gray
to black; anterior and posterior surfaces of thighs gray
or black.

Variation The adult paratypes and referred speci-


mens closely resemble the holotype. Body measure-
ments (in millimeters) of two adult paratypes (female Figure7. Schematic map showing the known distribution of
and male) and one subadult specimen are as follows: Scinax iquitorum sp.n. Square indicates the type locality. Shaded
areas indicate elevations above 500m a.s.l
SVL 38.5, 35.0, 20.5; tibia length 18.9, 16.9, 10.9;
foot length 14.8, 13.4, 7.8; head length 12.6, 11.6, 7.5;
head width 12.7, 11.8, 7.3; internarial distance 3.0,
2.7, 1.0; interorbital distance 4.0, 3.8, 2.3; width of sitting on leafs or palm trunks up to 150 cm high.
eyelid , 3.0, 1.8; diameter of eye 4.0, 3.9, 2.3; diame- Both adult females were gravid. The only collected
ter of tympanum 2.0, 1.8, 1.0. The pectoral fold of all male did not vocalize. Thirteen other hylid species
paratypes is less marked than in the holotype. Varia- (including Scinax garbei and S.ruber) were recorded
tion in foot webbing is I2(22+)II(11+)(22+)III12+ in the area of the type locality of S.iquitorum (see
IV2(11+)V. Number of teeth on vomerine dentiger- Moravec etal. 2002b), from which Dendropsophus
ous processes in adult paratypes (female, male) 5/8, parviceps, Hypsiboas microderma, Osteocephalus
6/7 (left/right). The male paratype (Fig.3) resembles planiceps, O.taurinus and S.garbei were found to
the females in all aspects except for the subarticular occur syntopically with the new species.
tubercles, which are more prominent (subconical to
conical), and supernumerary tubercles, which are Etymology The new taxon is dedicated to the na-
distinct. The shape of the vocal sac is unclear; nev- tive South American tribe called Iquito. In Peru the
ertheless it does not seem to be enlarged. The vocal Iquitos inhabit small settlements on the banks of the
slits extend from the lateral base of tongue (roughly Maran, Tigre, and Nanay rivers, which originally
in two-thirds of its length from the anterior edge) to included the entire area of todays town of Iquitos.
the angles of jaws. Coloration of paratypes is similar
to that of the holotype (Fig.2). Throat and chest of
the male paratype are yellow in life. Discussion

Distribution and ecology Scinax iquitorum is known The description of any new taxon of Scinax that
from the area of Rio Nanay and Peruvian Rio Yavari, occurs within the range of the widespread Scinax
Region Loreto, Peru (Fig.7). The type locality cor- ruber makes it unavoidable that one will deal with
responds to the area called Arboretum lying on the the several available names in the synonymy of this
right bank of the Rio Nanay at the village of Puerto species. Currently, seven available names are in the
Almendras. This territory is covered by disturbed pri- synonymy of Scinax ruber. These are Hyla lateristri-
mary rainforest and serves as a field study area of the ga Spix, 1824 (type locality: Brazil, by implication),
Universidad Nacional de la Amazona Peruana, Iqui- Hyla conirostris Peters, 1863 (type locality Suri-
tos (UNAP). The forest is not cleared but a permanent nam), Scytopis alleni Cope, 1870 (type locality State
dense grid of trails is maintained there. The area can of Par, Brazil, by lectotype designation of Duellman
be roughly divided into non-flooded and seasonally and Wiens, 1993), Scytopis cryptanthus Cope, 1874
flooded zones along the Rio Nanay. The collected (type locality Nauta, Region Loreto, Peru), Hyla
specimens were found at night in the non-flooded lineomaculata Werner, 1899 (type locality Arima,
zone of the closed forest (from its periphery to the Trinidad), Hyla rubra hbneri Melin, 1941 (type lo-
border of the flooded area). All the individuals were cality Taracu, Rio Uaupes, So Gabriel, Rio Ne-
14 New species of Scinax

gro, and Vicinity of Manaus, all localities in the Resumen


State of Amazonas, Brazil), and Hyla robersimoni
Donoso-Barros, 1965 1964 (type locality Pajona- Se describe una nueva especie del gnero hlido
les al sur de Macuro, Penisula de Paria, Venezuela). Scinax del norte del llano amaznico (rea de Iqui-
According to their original descriptions, all these tos, Region de Loreto, Per). La especie nueva per-
names are associated with specimens that have yel- tenece al clado de Scinax ruber y difiere del resto de
low blotches on the anterior and posterior surfaces of especies por tener la piel del dorso leve a fuertemen-
the thighs, and in some cases undersurfaces of tibiae. te granulado, por la ausencia de tubrculos ulnares y
Similarly, there are two available names in the tarsales conspicuos, por tener coloracin verde oliva
synonymy of S.funereus Hyla depressiceps Bou- en el dorso, flancos amarillo brillante con manchas
lenger, 1882 (type locality Ecuador) and Hyla ru- negras, superficie posterior de los muslos negra, y un
bra inconspicua Melin, 1941 (type locality Roque, iris color dorado a bronce.
Region San Martn,, Peru). According to the original
description, H.depressiceps differs from the new tax-
on in having a dark canthal stripe and black and whit- Acknowledgements
ish marbled limbs. An examination of the holotype of
Hyla rubra inconspicua shows that it differs by the Special thanks to William E. Duellman (University of Kansas,
presence of small tubercles on the head, dorsum and Lawrence), Dr. Ignacio De la Riva (Museo Nacional de Ciencias
Naturales, Madrid) and Julin Faivovich (American Museum of
limbs, presence of a dark canthal stripe, transverse
Natural History) for their valuable comments in the determination
bars on dorsum of limbs and by its larger size (SVL of the new species. We are grateful to Wolfgang Bhme (Zoolo-
45mm). gisches Forschungsmuseum A. Koenig, Bonn) for the kind loan
The consideration of Scinax fuscomarginatus as of comparative material and William E. Duellman for providing
an Amazonian component is based solely on the fact comparative photographs of Scinax funereus and S.cruentomus.
We thank Karen Siu-Ting (Museo de Historia Natural Universi-
that Lutz (1973) included Hyla parkeri Gaige, 1926
dad Nacional Mayor de San Markos, Lima) for kind translation
(type locality Buenavista, Bolivia) and Hyla madeirae of the abstract into Spanish and two anonymous referees for their
Bokermann, 1964 (Type locality Porto Velho, Estado valuable comments on the manuscript. Work of JM was support-
de Rondnia, Brazil) in the synonymy of Hyla fusco- ed by the project MK00002327201 and conducted in cooperation
marginata A. Lutz, 1925 (type locality restricted by with the Museo de Zoologia UNAP, Iquitos (Andrs Mrmol
Burgos, research authorization N4522000INRENALoreto)
Lutz [1973] to Belo Horizonte, State of Minas Gerais,
under the auspices of the Universidad de la Amazona Peruana,
Brazil). Although De La Riva etal. (1997), recently Iquitos (the agreement signed by Jos Torres Vsquez and Milan
resurrected Scinax parkeri for the Bolivian popula- Stloukal).
tions, the status of the Amazonian form, previously
named Scinax madeirae, is still unclear as discussed
by these authors. A similar problem occurs with Sci- Literature Cited
nax trilineatus (Hoogmoed and Gorzula, 1979) (type
locality 12km SE. El Manteco, Estado Bolvar, Ven- Boulenger, G. A. 1882. Catalogue of the Batrachia Salientia
ezuela), later suggested to be a synonym of S.fusco- s. Ecaudata in the collection of the British Museum. Ed.2.,
marginatus by Martins (1998) without further com- London. (reprinted: Wheldon and Wesley, ltd. and Verlag J.
ments. Regardless of these remaining problems, it is Cramer, 1966)
Cope, E. D. 1870. Seventh contribution to the herpetology of
clear that none of these names is assignable to the new tropical America. Proceeding of the American Philosophical
species being described here, since they are all associ- Society Society, 11[1869]:147169.
ated with forms resembling S.fuscomarginatus. Cope, E. D. 1874. On some Batrachia and Nematognathi brought
The territory of the Arboretum represents an from the upper Amazon by Prof. Orton. Proceedings of the
important refuge for the relatively diverse local her- Academy of Natural Sciences of Philadelphia, 26:120137.
De la Riva, I. 1990. Una especie nueva de Ololygon procedente
petofauna (36 species of amphibians and 13 species de Bolivia. Revista Espaola de Herpetologa, 4:8186.
of reptiles) situated at the edge of densely populated De La Riva, I., R. Marquez, and J. Bosch. 1997. Description
farmland. Recently, human activity has increased of the advertisement calls of some South American Hylidae
considerably in the area of Puerto Almendras because (Amphibia, Anura): taxonomic and methodological
a new modern University campus was built between consequences. Bonner Zoologische Beitrge, 47:175185.
De la Riva, I., J. Khler, S. Lters, and S. Reichle. 2000. Ten
the Arboretum and the bank of Rio Nanay. There- years of research on Bolivian amphibians: updated checklist,
fore, an effective protection of the type locality of distribution, taxonomic problems, literature and iconography.
Scinax iquitorum is desirable. Revista Espaola de Herpetologa, 14:19164.
Moravec, J. etal. 15

Donoso-Barros, R. 1965. Nuevos reptiles y anfibios de Moravec, J., I. Arista Tuanama, and A. Mrmol Burgos. 2002a.
Venezuela. Noticiario Mensual Museo Nacional de Historia Reptiles recently recorded from the surroundings of Iquitos
Natural (Santiago, Chile) 9, No.102, 2 unnumbered pp. (Departamento Loreto, Peru). asopis Nrodnho Muzea,
Duellman, W. E. 1970. The hylid frogs of Middle America. ada prodovdn, 170[2001]:4768.
Museum of Natural History, University of Kansas, Monograph Moravec, J., I. Arista Tuanama, and A. Mrmol Burgos.
1:1753, plates 172 (2 volumes). 2002b. Amphibians recently recorded from the surroundings
Duellman, W. E. 1971. The identities of some Ecuadorian hylid of Iquitos (Departamento Loreto, Peru). I. Hylidae. asopis
frogs. Herpetologica, 27:212227. Nrodnho Muzea, ada prodovdn, 171:2944.
Duellman, W. E. 1972. South American frogs of the Hyla Myers, Ch. W., and W. E. Duellman. 1982. A new species of
rostrata group (Amphibia, Anura, Hylidae). Zoologische Hyla from Cerro Colorado, and other tree frog records and
Mededelingen, 47:177192. geographical notes from Western Panama. American Museum
Duellman, W. E. 2001. The hylid frogs of Middle America. SSAR, Novitates No. 2752:132.
Ithaca, New York, xvi+1159, plates 192 (2 volumes). Peters, W. 1863. Mitteilungen ber neue Batrachier.
Duellman, W. E., J. J. Wiens. 1992. The status of the hylid frog Monatsberichte der Kniglich Preussischen Akademie der
genus Ololygon and the recognition of Scinax Wagler, 1830. Wissenschaften zu Berlin, 1863:445470.
Occasional papers of the Museum of Natural History, The Pombal Jr., J. P., C. F. B. Haddad, and S. Kasahara. 1995. A
University of Kansas, Lawrence, Kansas, 151:123. new species of Scinax (Anura: Hylidae) from Southeastern
Duellman, W. E., J. J. Wiens. 1993. Hylid frogs of the genus Brazil, with comments on the genus. Journal of Herpetology,
Scinax Wagler, 1830, in Amazonian Ecuador and Peru. 29:16.
Occasional papers of the Museum of Natural History, The Pyburn, W. F. 1992. A new tree frog of the genus Scinax from
University of Kansas, Lawrence, Kansas, 153:157. the Vaupes river of northwestern Brazil. The Texas Journal of
Faivovich, J. 2002. A cladistic analysis of Scinax (Anura: Science, 44: 405411.
Hylidae). Cladistics, 18:367393. Rivero, J. A. 1961. Salientia of Venezuela. Bulletin of the
Frost, D. R. 2008. Amphibian species of the world: an online Museum of Comparative Zoology, 126:1207.
reference. Version 5.2, American Museum of Natural Savage, J. M., and R. W. Heyer. 1967. Variation and distribution
History, New York, USA. Available at http://research.amnh. in the treefrog genus Phyllomedusa in Costa Rica, Central
org/herpetology/amphibia/index.php. (15 July, 2008) America. Beitrge zur Neotropischen Fauna, 5:111131.
Goin, C. J. 1966. Description of a new frog of the genus Hyla Savage, J. M., and R. W. Heyer. 1997. Digital webbing formulae
from Suriname. Zoologische. Mededelingen, 41:229232. for anurans: A refinement. Herpetological Review, 28:131.
Hoogmoed, M. S., and S. Gorzula. 1979. Checklist of the savanna Spix, de, J. B. 1824. Animalia Nova sive species novae
inhabiting frogs of the El Manteco region with notes on their Testudinum et Ranarum, quas inintinere per Brasiliam annis
ecology and the description of a new species of treefrog. MDCCCXVIIMDCCCXX jussu et auspiciis Maximiliani
Zoologische Mededelingen, 54:183216. Josephi I. Bavariae Regis. Monachii, F.S. Hbschmann,
Lutz, B. 1973. Brazilian species of Hyla. University of Texas 4+53pp, 17+122pls.
Press, Austin and London, xviii+260+5pp. Werner, F. 1899. Ueber Reptilien und Batrachier aus Columbien
Martins, M. 1998. The frogs of Ilha de Maraca. Pp.285306. In und Trinidad. Verhandlungen der kaiserlich-kniglichen
W. Milliken, and J. A. Ratter (Eds.), Maraca. The biodiversity zoologisch-botanischen Gesellschaft in Wien, 49:470484.
and environment of an Amazonian rainforest. John Wiley and
Sons. Submitted 16 November 2008
Melin, D. 1941. Contribution to the knowledge of the Amphibia Accepted 10 March 2009
of South America. Gteborgs Kungliga Vetenskaps och
Vitter-Hets Samhalles Handligar (6) 1B(4):171.
16 New species of Scinax

Appendix 1

Specimens Examined

Hyla rubra hbneri: Brazil: GNM 478 (syntype): State of Amazonas: vicinity of Manaus.

Hyla rubra inconspicua: Peru: GNM 480 (holotype): Region de San Martn: Roque.

Scinax cruentommus: ECUADOR: KU 126587 (holotype), KU 105157, 105163, 105167, 105180, 105182,
10702224, 109508, 10951217, 10951921 (paratypes): Provincia de Sucumbios: Santa Cecilia, 340m; KU
120976: Provincia de Pastaza: Mera, 1100m; KU 12660910: Provincia de Sucumbios: Lago Agrio, 370m;
KU 135485: Provincia de Zamora-Chinchipe, 10km W Zamora, 1200m; KU 146297, 150093102, 15243538,
152447: Provincia de Sucumbios: Santa Cecilia, 340m; KU 17517677: Provincia de Orellana: Rio Yasuni,
150km upstream from Rio Napo, 180m; KU 175177: Provincia de Orelana: Rio Yasuni, 200km upstream from
Rio Napo, 180m; KU 17863542, KU 18362334, 183674: Provincia de Sucumbios: Limnococha, 200m; KU
217699: Provincia de Morona-Santiago: 1.2km N Gualaquiza, 850m; KU 217700: Provincia de Sucumbios:
2.5km N Lago Agrio, 350m; KU 217701: Provincia de Napo: Jatun-Sacha, 420m; KU 29601320: Provin-
cia de Sucumbios: Lago Agrio. PERU: KU 172143: Region Hunuco: Rio Llullapichis, 45km upstream from
Rio Pachitea, Finca Panguana; KU 19201820: Region Loreto: Rio Samiria, Estacion Biologica Pithecia; KU
22033641: Region Loreto: Explorama Lodge, junction Rio Yanamono and Rio Amazonas; KU 220431: Re-
gion Loreto: Explorama Lodge, junction Rio Sucusari and Rio Napo; KU 220560: Region Loreto: Rio Tahuayo,
3060km upstream from Rio Amazonas; KU 22195859: Region Loreto: Teniente Lopez, 200m; KU 222342:
Region Loreto: Explorama Lodge, junction Rio Yanamono and Rio Amazonas, 180m.

Scinax funereus: Colombia: AMNH 11622122: Departamento Putumayo: upper Rio San Miguel: Santa Rosa de
Sucumbos (Kofan village). ECUADOR: KU 111929, 111970, 12312128, 12639397, 146298301, 15014975,
15244346: Provincia de Sucumbios: Santa Cecilia, 340m; KU 178645: Provincia de Napo: Limnococha: 243m;
KU 18363538: Provincia de Napo: Limnococha; KU 9922122: Provincia de Sucumbios: Limnococha, 300m;
KU 1015962, 10516466, 10516879, 105181, 10518387, 10952223: Provincia de Sucumbios: Santa Ceci-
lia, 340m; KU 2177702: Provincia de Napo: Jatun Sacha, 420m; KU 22166869: Provincia de Orelana: Coca.
PERU: KU 15468081, 154728: Region de Madre de Dios: Cocha Cachu: Rio Manu between Rio Panguana and
Rio Cachiri, 400m; KU 19875: Region Loreto: Rio Curanja, Balta; KU 217304: San Martin: Lamas, 14.5km SW
Zapatero, 870m; KU 221960: Region Loreto: San Jacinto, 175m; KU 221961: Region Loreto: Teniente Lopez,
200m; voucher photo NMP6F 7: Region Loreto, Rio Curaray, 014540S, 0750411W.

Scinax garbei: PERU: NMP6V 71150: Region Loreto: 17km SW of Iquitos: vicinity of the village of Puerto Al-
mendras); NMP6V 71151: 23km SW of Iquitos: Sacha Mama; NMP6V 71266/12: 31km SW of Iquitos.

Scinax cf. ictericus: Peru: ZFMK 39353: Region Madre de Dios: Rio Tambopata: Bajo Tambopata; ZFMK 39361,
39363: Rio Tambopata: ZFMK 39366: Aguajalito; Rio Tambopata: Tres Chimbadas.

Scinax nebulosus: Bolivia: NMP6V 70894: Departamento Beni: 2km W of Riberalta.

Scinax pedromedinae: BOLIVIA: NMP6V 70700: Departamento Beni: 5km NE of Riberalta.

Scinax ruber: Bolivia: NMP6V 70895/17: Departamento Beni: 68km NE of Riberalta. PERU: NMP6V
71152/14, 71191: Region Loreto: 17km SW of Iquitos: vicinity of the village of Puerto Almendras; NMP6V
71145: 23km SW of Iquitos: Sacha Mama; NMP6V 71265: 31km SW of Iquitos.

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