RE- : SERPENTES:

Catalogue of American Amphibians and . between supraorbitals 4-15; loreals 2-5; subloreals 2-10; loreals + subloreals 2-14; circumorbiil scales 9-19; nasals uusally in contact Henderson, RW. 1993. Comllus caninur with 3-12 scales bordering nasals. Virtually no sexual dimorphism exists in traditional meristic characters. The dorsal ground color in juveniles is yellow (rarely retained in adults), brick red-brown, or, rarely, green; in adults ground color is canina Linnaeus, 1758:215. m-locality, 'America." Holo- some shade of green. The transition from juvenile to adult coloration type, Naturhistoriska Riksmuseet, Stockholm (MS) Li. 8, col- (based on wildcaught specimens) is gradual and usually occurs in lector and date of collection unknown, sex and age status un- 550-600 mm SVL, although they may be as small as 450-500 known (not examined by author). mm SVL. The ventral ground color in juveniles usually is beige or BoaHipnale Limaeus, 1758:215. Type-locality 'Asia." Holotype, not dingy yellow and usually immaculate. In adults, the ventral ground traced. color is off-white, cream, or some shade of yellow (dingy to bright); Boa tbahrsina Laurenti, 1768:89. Substitute name for Boa canina ventrals and subcaudals usually are immaculate, but may occasion- Limaeus. ally be flecked with some shade of green. The underside of the head Boa aumntiaca Iaurenti, 1768:89. Type-locality, -America." Holo- usually is some shade of yellow, immaculate or flecked or washed type, not traced. with green (sometimes quite heavily). The labials are some shade of Boa erigua Laurenti, 1768:89. Substitute name for Boa bipnale Lin- yellow and are frequently flecked or washed with green. The ventral naeus. ground color encroaches onto the dorsal scale rows, with more Xipbacorna arammbqya Wagler in Spix, 1824:45. Type-locality, anterior than posterior scale rows affected. The encroaching yellow 'aquis flumini Negro, Arnazonum laterali." Holotype, Zoologi- is usually flecked with green, sometimes heavily. Enamel white sche Staatssammlung, Munich, 1365/0, collector and date of markings usually are present laterally and dorsally. The dorsalmost collection unknown, adult, sex unknown (not examined by au- markings usually are triangular inshape, with the base ofthe triangle thor). on the dorsal midline; the triangles may be connected by a middorsal Xipbaroma canina: Fizinger, 1843:24. line or not connected. The triangles are often absent anteriorly Cbrysemis batesii Gray, 1860:132. Type-locality, 'Upper Amazon." (resulting in no anterior pattern or just a middorsal stripe, either Holotype, British Museum (Natural History) (BMNH) 59.12.28. continuousor broken), becoming prominent and elongate at midbody 12., collector and date of collection unknown, sex and size un- (to the point of losing the triangular shape and appearing as white known (not examined by author). lines perpendicular to the dorsal midline); posteriorly, triangles are Comllur caninus: Boulenger, 1893:102. shorter and broader. Frequently thedorsal ground color surrounding the triangles is heavily stippled withdark green to black in adults, and Content Coralluc caninus is monotypic. brown in yellowish juveniles. Lateral blotches may be absent or greatly reduced anteriorly, becoming more prominent at midbody Definition. Maximum SVL is at least 1530 mm. The general and posteriorly. Considerable geographic variation exists in the habitus is with a large, chunky head, long anterior maxillary teeth, extent of the lateral white blotches: snakes from eastern Venezuela, slender neck, stronglylaterally compressed body, and prehensiletail. Guyana, Suriname, and mnheastern Brasil (Roraima) frequentlylack Dorsal scale rows at midbody number 60-84; ventrals 186-218; lateral markings or have them much reduced; snakes from western subcaudals 62-84; ventrals + subcaudals 256-285; supralabials (with Brasil (RondBnia, Maao Grosso) also may lack lateral white markings. deep labiil pits) 9-13, infralabials (with deep labial pits) 11-16; scales In extreme cases (snakes from Guyana), the dorsum is devoid of any

Map. Distribution of ComNur caninus The type-locality is undetermined. Questionable locality records are noted by question marks. Figure 1. Juvenile ComUus caninus from Santa Cecilia, Napo, Ecuador. Note the presence of lateral white markings. Photograph by W.E. Duellman. white markings. In contrast, snakes from Amazonia (exceptions (1979), Lancini V. (19791, Colder (19851, Maaison (1986), Stafford noted) have conspicuous lateral white blotches, especially pro- (1986), Mehnens (1987), Perez-Santos and Moreno (19881, Campbell nounced in snakes from the the easternmost region of Amazonia and Lamar (1989), Ross and Marzec (19901, and Perez-Santos and (MaranMo) and the upper Amazon of Ecuador and Peru, but with Moreno (1991). Black and white drawings of the head are in Roze frequent exceptions. In extreme cases, the normally dorsoventrally (1966) and full body drawings are found in Wagler, in Spbr (18241, oriented elongate blotches (1-2 scales wide x 4-10 scales long) are Gray (1860), and Perez-Santos and Moreno (1988). Color drawings almost round and may be 4 x 4 scales in dimension. are presented in Amaral(1976). Drawings of cranial elements occur The hemipenis (based on a specimen from Brasil) is shallowly in Frazzetta (1975) and Kluge (1991). A drawing of a lung appears in forked, extending to the 9th subcaudal, the organ diiding at the 7th Beddard (1908). subcaudal and the sulcus diiding at the 6th subcaudal. The basal one-third is nude with prominent sulcal folds. Dilly, six flounces DistrIbutloa ComUus caninus is restricted to Amazonian fuse with the sulcal folds and are most prominent on the sulcal and Guianan South America: Colombia, Venezuela (the record from surface; the flouncesoccur before the bifurcation. The most proximal Caripito, Monagas in Roze I19661 is based on a misidentified ComUus flounce is reduced in size and extended into a small m~illaon the mydd), Ecuador, Peru, Bolivia, Brasil, Guyana, Suriname, and asulcate surface. The sulcal folds extend to the tips of ;hi shon arms French Guiana. A questionable published record from west of the (which bear only a few papillate flounces) (Branch, 1981). Andes was cited by Niceforo Maria (1942). Altitudinal distribution is from sea level to about 1000 m. The distribution of C. caninus is Diagnosis. ComUus caninus is characterized by 186-218 largely coincident with the diributionof lowland vopical rainforest. ventrals, compared to >250 in C. annulatus and C. en#& Dorsal The species is absent from caatinga and Atlantic coastal forest in scale rows number CM4 at midbody, compared to 37-57 in C. eastern Brasil. ComUus caninus occurs only in areas that receive annulatus and C. en#&. Comllus cmpanii, the sister species of C. >I500 mm of precipitation annually. caninus (Kluge, 1991), has only 29-30 dorsal scale rows at midbody. Juvenile (yellow) C. caninus bear a superficial resemblance to Fossil Record. None. yellow phase C. en$&, but scale characters easily distinguish the two taxa. Pment Literature. A comprehensive account of the biology of Comllus caninus is not available. Various reports on Descriptions. General descriptions are many and vary in aspects of the biology of C. caninus have appeared as follows: usefulness; arranged by country: Colombia @urn, 1944; Perez- chromosomes (wak, 1965;Gomn and Cress, 1970), bile acids Santos and Moreno, 19881, Venezuela (Roze, 1966,1970; Lancini V., (Haslewood and Woonon, 1951; Haslewood, 1%7), scent gland 1979), Guyana (Beebe, 1946), Suriname (Moonen et al., 19791, lipids (Tolson, 1987), cranial osteology (Frazzetta, 1959; McDowell, French Guiana (Chippaux, 1986), Ecuador (Duellman, 1978; Perez- 1979; Kluge, 1991), soft anatomy (Beddard, 1908; Underwood, 1967; Santos and Moreno, 1991), Peru (Carrillo de Espinoza, 1966, 1970; Kluge, 1991), radiant heat reception (Bullock and Barrea, 19681, Dixon and Soini, 1976, 1986), Brasil (Wagler, in Spix, 1824; Amaral, hemipenis(McDowell, 1979; Branch, 1981), counship(Murphyetal., 1976; Cunha and Nascimento, 1978; Santos, 1981). 1978), reproduction (Murphy etal., 1978; Gobels, 1985; Schulte, 1988; Ross and Marzec, 1990), ontogenetic color change (Gobels, 1985; IIlustradons. Many photographs of this spectacular Colder, 1985; Schulte, 1988), habitat (Cunha and Nascimento, 1978; have been published, and no useful purpose would be served in Duellman, 1978; Hoogmoed, 1979; Perez-Santos and Moreno, 1988, attempting to list them all. Black and white photographs appear in 1992; Duellman, 1989,1990;RodriguezandCadle, 1990; Zimmerman Dinmars (1942), Beebe (19461, Carrillo de Espinoza (1%6), Cunh and Rodrimes, lm), diil activity (Cunha and Nascimento, 1978; and Nascimento (1978), and Duellman (1978). Color photographs ~uellman;1989,1990; Rodriguez and Cadle, 1990; Zimermzn and appear in Schmidt and Inger (1%7), Roze (1970), Moonen et a1. Rodrigues, lm), defensive behavior (Greene, 1988), stereotyped Note the lack of lateral white markings and the presence behavior (Carpenter and Ferguson, 1977), diet (Cunha and Carpenter, C.C. and G.W. Ferguson. 1977. Variation and evolution of Nascimento, 1978; Duellman, 1989,1990;RodriguezandCadle, 1990; stereotyped behavior in reptiles, pp. 335554. In C. Cans and Zimrnerman and Rodrigues, 1990; Henderson, 1993), population D.W. Tinkle (eds.), Biology of the Reptilia, Vol. 7, Ecology and density (Schulte, 1988), phylogeny (Frazzetta, 1975; Kluge, 19911, behaviour A. Academic Press, New York. conservation strategy (Schulte, 19881, captive maintenance and be- Carrillo de Espinozl, N. 1966. Contribucion al conocimiento de 10s havior (Osborne, 1984; Gobels, 1985; Colder, 1985; Wagner, 1985; boideos Peruanas (Boidae, Ophidia, Reptilia). Publ. Mus. Hist. Stafford, 1986; Schulte, 1988; Blody and Mehaffey, 1989; Ross and Nat. "Javier Prado", Ser. A., Zool. 21:86-136. Marzec, lm), frequency of shedding and defecation (Gehrmann, -. 1970. Contribucion al conocimiento de 10s reptiles del Peru. 1990). Publ. Mus. Hist. Nat. "Javier Prado", Ser. A., Zool. 22:1-64. Etymology. The spec if^ name caninus is Latin, meaning'of dogs," and likely refers to the dog-like appearance of the head, including the long anterior maxillary teeth.

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Variation in the periodicity of defecation and Fondo Cultura Cientif., Caracas. ecdysis in agroupofsiblingemeraldtreeboas, Comlluscaninur Santos, E. 1981. Anfibios e repteis do Brasil (vida e costumes). Edih. Bull. Chicago Herpetol. Soc. 25:67-69. Itatiaia Ltda., Belo Horizonte. Gobels, M. 1985. Haltung und Nachzucht des Hundkopfschlingen Schmidt, K.P. and R.F. Inger. 1957. Living reptilesofthe World. Dou- ComNus caninus Limaeus, 1758 imTemrium. Salamandra 21: bleday & Co., Inc., Garden City, NY. 137-147. Schulte, R 1988. Observaciones sobre la boaverde, CoralIuscaninus, Golder,F. 1985.HaltungundZucht sowieUmfarbungderJungschhg en el Depanamento San Manin-Peru. Bol. Lima 5521-26. en von Comllus caninus (Liinaeus, 1758). Salamandra 21:14& Spix, J.B. von. 1824. Serpentum brasiliensium species novae ou his- 1%. toire naturelle des es@ces nouvelles & serpens, recueillies et Gorman, G.C. and F. 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Mus. 2.001. Univ. Michigan 178: iv + 58 p. Robert W. Hendemon, Section of Vertebrate Zoology, Milwaukee Lancini V., A.R 1979. Serpientes de Venezuela. Graf~asArmitano, Public Museum, 800 W. Wells Street, Milwaukee, Wisconsin 53233. Caracas. Laurenti,J.N. 1768. Specimenmedicum, exhibenssynopsin reptilium prima,,, editor for this account, brry w,lson. mendatumcumexperimentiscircavenena et antidota reptilium ausuiacorum. ~oan.Thom. Nob de Trannern, Viemae.' Published30November 1993andCopyright O 1993by the Society for Limaeus, C. 1758. Systema naturae per regna tria naturae, xcundum the study of~mphibiansand ~~~il~~. classes,ordines, genera, species, cumcharaderibus, differentiis,