You are on page 1of 1

Natural History Notes 447

Of particular interest is the position of the snake along the

PHOTO BY M. Wachlevski
stick (Fig. 1). It was motionless and oriented head-down in a
position similar to that often described as ambush posture for
some arboreal snake species (e.g., Corallus spp., Henderson
2002. Neotropical Treeboas. Krieger Publ. Co., Malabar, Florida.
197 pp.). The snake was found after several hours of rain beside
a dry riverbed and we suspect that it was using the stick perch
as a vantage point from which to scan for snails and slugs mov-
ing in the damp leaf litter below. Preliminary data from a feeding
behavior study led by CMS support this hypothesis in that cap-
tive T. philippii often use visual cues to initially locate and follow
molluscan prey.
We thank J. A. Campbell for assistance, and G. N. Weather-
man for assistance with field work. The National Science Foun-
dation (DEB-0613802) provided financial support.
COLEMAN M. SHEEHY III (e-mail: cmsheehy@uta.edu), JEFFREY W.
STREICHER, CHRISTIAN L. COX, and JACOBO REYES-VELASCO, Amphib- Fig. 1. An adult female Xenodon neuwiedii found preying on a Rhi-
ian and Reptile Diversity Research Center, Department of Biology, Univer- nella abei in the Parque Estadual da Serra do Tabuleiro, Brazil.
sity of Texas at Arlington, Arlington, Texas 76019, USA.
Holos, Ribeirão Preto; Sazima and Haddad 1992. In Morellato
TROPIDONOPHIS DORIAE (Barred Keelback). ENDOPARA- [ed.], História Natural da Serra do Japi: Ecologia e Preservação
SITES. Tropidonophis doriae is known from Indonesia (Irian, de uma Área Florestal no Sudeste do Brasil, pp. 212–236. FAPESP,
Java, Aru Islands) and Papua New Guinea (Malnate and Under- Campinas). However, anurans belonging to other families (Hy-
wood 1988. Proc. Acad. Nat. Sci. Philadelphia 140:59–201). It is a lidae, Leptodactylidae, and Cyclorhamphidae) and even lizards
terrestrial, nocturnal predator that eats frogs and fish (Malnate (Enyalius sp.) are occasionally consumed (Hartmann et al. 2009.
and Underwood, op. cit). To our knowledge there are no reports Biota Neotrop. 9:173–184; Marques and Sazima, op. cit.). Rhinel-
of helminths for T. doriae. The purpose of this note is to estab- la abei is a frog distributed in the southern Atlantic Rainforest
lish an initial helminth list for T. doriae. Two T. doriae from the from Paraná state to southern Santa Catarina state and northern
herpetology collection of the Bishop Museum (BPBM), Hono- areas of Rio Grande do Sul state, Brazil (Baldissera Jr. et al. 2004.
lulu, HI, USA each had nematodes protruding from a slit in their Arq. Mus. Nac., Rio de Janeiro 62[3]:255–282). Here we report the
body walls (BPBM 31526, SVL = 254 mm; BPBM 31527, SVL = predation of the frog R. abei by the snake X. neuwiedii.
327 mm). Both snakes were collected on 3 April 2007 in Madang On 16 January 2009, in the Parque Estadual da Serra do Tabu-
Province, Wanang, Papua New Guinea (5.232118°S, 145.18068°E; leiro, Santo Amaro da Imperatriz municipality, Santa Catarina
datum: WGS84; elev. 600 m). Nematodes were removed, cleared state, Brazil (27.7427°S, 48.8075°W, datum: SAD 69), an adult fe-
in glycerol, placed on glass slides, coverslipped, studied under male X. neuwiedii (SVL = 489 mm; tail length = 113 mm; 59.5 g),
a compound microscope and identified as Tanqua anomala was found at 1015 h on leaf litter in an area of dense ombrophi-
(eight from BPBM 31526) and (six from BPBM 31527). Voucher lous forest ingesting an adult R. abei (SVL = 69.1 mm; 26.2 g; 44%
helminths were deposited in the United States National Para- of the snake’s mass). The frog was being ingested headfirst, ven-
site Collection (USNPC), Beltsville, Maryland, USA as USNPC tral side up, and was still alive (Fig. 1). Manipulation of the snake
(103501) and the Bishop Museum (BPBM) as (H423). Tanqua resulted in the release of the prey, which presented deep wounds
anomala is common in snakes from southeast and southern Asia in the abdominal region. Batracophagy seems to be the most fre-
(Baker 1987. Occas. Pap. Mem. Univ. Newfoundland 11:1–327; quent feeding habit of Xenodon (Marques et al. 2001. Serpentes
Sood 1999. Reptilian Nematodes from South Asia, International da Mata Atlântica. Guia Ilustrado para a Serra do Mar. Ribeirão
Book Distributors, Dehra Dun, India. 299 pp.). There is a record Preto, Editora Holos. 184 pp.) and some species have special-
of a larval T. anomala in Hoplobatrachus tigerinus (= Rana tig- ized skulls and dentition, facilitating the capture and ingestion
rina) in Baker (op. cit). As T. doriae feeds on frogs, frogs may act of frogs (Kardong 1979. Evolution 33:433–443). The wounds we
as paratenic (= transport hosts) for T. anomala. Tanqua anomala observed are evidence of the functionality of X. neuwiedii’s en-
in T. doriae is a new host record. Papua New Guinea is a new lo- larged posterior teeth, which allow perforation of the prey and
cality record. the consequent evacuation of air, which is accumulated in the
We thank Pumehana Imada (IBPBM) for facilitating our ex- toad’s body for defense (Amaral 1978. Serpentes do Brasil, Icono-
amination of T. doriae. grafia Colorida, 2a edição. Melhoramentos/EDUSP, São Paulo.
STEPHEN R. GOLDBERG, Whittier College, Department of Biology, PO 247 pp.).
Box 634, Whittier, California 90608, USA (e-mail: sgoldberg@whittier.edu); THIAGO MAIA (e-mail: thiagomaianc@gmail.com), MILENA
CHARLES R. BURSEY, Pennsylvania State University, Shenango Campus, WACHLEVSKI (e-mail: milenawm@yahoo.com), LUCIANA BARÇANTE (e-
Department of Biology, Sharon, Pennsylvania 16146, USA (e-mail: cxb13@ mail: lubarcante@hotmail.com), and CARLOS F. D. ROCHA (e-mail: cfdro-
psu.edu). cha@uerj.br), Departamento de Ecologia, Universidade do Estado do Rio
de Janeiro, Rua São Francisco Xavier 524, CEP 20550-013, Rio de Janeiro,
XENODON NEUWIEDII (False Lancehead). DIET. The dipsadid Brazil.
snake Xenodon neuwiedii has a diet composed predominantly
of anurans, especially those in the genus Rhinella (Marques and
Sazima 2004. In Marques and Duleba [eds.], Estação Ccológica
Juréia-Itatins: Ambiente Físico, Flora e Fauna, pp. 257–277.

Herpetological Review 42(3), 2011

You might also like