Monday, June 27, 2016

Yellow Puffing Snake, Spilotes sulphureus (Family Colubridae)

Natrix sulphurea Wagler 1824: 26
Coluber poecilostoma Wied-Neuwied 1824
Spilotes poecilostoma — Duméril, Bibron & Duméril 1854: 221
Phrynonax sulphureus — Boulenger 1894: 19
Pseustes sulphureus sulphureus — Beebe 1946: 41
Pseustes sulphureus — Gasc & Rodrigues 1980

Spilotes sulphureus — Jadin et al. 2013.

Size: 977 mm SVL, 1,424 mm TL, may exceed 3.0 m; tail about 45% of SVL; hatchlings relatively large 350–518 mm SVL.

Identification: Dorsal scales in 21 rows at mid-body reduced to 13 or 15 posteriorly; all rows keeled except the first two. This is a large black snake that may have yellow cross bands or spots on the anterior body, or the body may be more yellow than black.

Similar species: In Trinidad it is most easily confused with Clelia or Drymarchon, none of these have dorsal scales in 21 rows. Rostral visible from above; nasals semi-divided; loreal single; one preocular; three postoculars; eight upper labials, 10 lower labials; ventrals 208−226; single cloacal plate; divided subcaudals 125−145; dorsal scales smooth with apical pits.

Habitat: Forest canopy snake, probably rarely comes to the ground. Biology: Diurnal, mostly arboreal species that is uncommon. Diet includes most vertebrates (reptiles, birds and mammals) it can swallow. Reproduction: Females reported to lay eggs in August with young hatching in October after 84–86 days of incubation.

Boos, H.E.A. 2001. The snakes of Trinidad and Tobago. Texas A&M University Press, 270 pp.
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Jadin, R. C., Burbrink, F. T., Rivas, G. A., Vitt, L. J., Barrio-Amorós, C. L. and Guralnick, R. P. 2013. Finding arboreal snakes in an evolutionary tree: phylogenetic placement and systematic revision of the Neotropical birdsnakes. Journal of Zoological Systematics and Evolutionary Research. 52 (3): 257–264; doi: 10.1111/jzs.12055.
Marques, O. AV Calleffo, Myriam E. 1997. Geographic Distribution. Pseustes sulphureus. Herpetological Review 28 (3): 160.
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Natera-Mumaw, Marco; Luis Felipe Esqueda-González & Manuel Castelaín-Fernández 2015. Atlas Serpientes de Venezuela Santiago de Chile, Dimacofi Negocios Avanzados S.A., 456 pp.
Oliveira Lula Salles, R. de & Silva-Soares, T. 2010. Répteis do município de Duque de Caxias, Baixada Fluminense, Rio de Janeiro, Sudeste do Brasil. Biotemas, 23 (2): 135-144
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Whithworth, A. & Beirne, C. 2011. Reptiles of the Yachana Reserve. Global Vision International, 130 pp. 

Flat Snake, Siphlophis compressus (Family Dipsadidae)

Coluber compressus Daudin 1803: 247.
Trypanurgos compressus — Beebe 1946: 43.
Tripanurgos compressus — Peters & Orejas-Miranda 1970: 311.

Siphlophis compressus — Zaher & Prudente 1999.

Type locality: Surinam.

Distribution: In Central America from Costa Rica to  Panama, southward into Colombia, Ecuador and Peru and eastward into Venezuela, Trinidad, and the Guianas and southward into  Brazil. 

This is a semi-arboreal snake that specializes in feeding on lizards. Mainland populations are frequently observed in arboreal habitats. On Trinidad most of the specimens we observed were on the ground at night or in the early morning hours.

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Barreto-Guedes, T. Geziana Silva SN, N Lúcia da Costa Prudente and OAV Marques 2011. New records and geographical distribution of the Tropical Banded Treesnake Siphlophis compressus (Dipsadidae) in Brazil. Herpetology Notes 4: 341-346
Barrio-Amorós CL., Chacón-Ortiz A., Diasparra, JP, Orellana, AM,  Bautista J. & Molina C. 2010. Distribution of Siphlophis compressus (Daudin, 1803) in Venezuela with a remarkable geographic extension [Short Note]. Herpetozoa 23: - get paper here
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Cortés Gómez, Angela María; Anyelet Valencia Aguilar, Diana Marcela Torres Domínguez, Lina María García Calderón, Diego Fernando Villaquirán Martínez, Andrea del Pilar Cáceres Franco, Fernando Castro Herrera 2010. Guía de los anfibios y reptiles. Área en conservación de la microcuenca Quebrada Pericos. [Valle de Cauca, Colombia]. Corporación Autónoma Regional del Valle del Cauca, Santiago de Cali: CVC, 37 pp.
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Gasc & Rodrigues 1980. Liste preliminaire des Serpents de la Guyane francaise. Bull. Mus. Nat. Hist. Nat. Paris 2 (4): 559-598.
Hamdan, B. & R. M. Lira-da-Silva 2012. The snakes of Bahia State, northeastern Brazil: species richness, composition and biogeographical notes. Salamandra 48 (1): 31-50.
Jenner, J. V.; Dowling, H. G. 1985. Taxonomy of American Xenodontine snakes: the tribe Pseudoboini. Herpetologica 41 (2): 161-172.
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Lancini,A.R. & Kornacker,P.M. 1989. Die Schlangen von Venezuela. Armitano Editores C.A., Caracas, 1-381
McConnell, G.J. 2013. A field guide to the snakes of Costa Rica. Edition Chimaira, 233 pp.
Mendes-Pinto, T. J. & S. Marques de Souza 2011. Preliminary assessment of amphibians and reptiles from Floresta Nacional do Trairão, with a new snake record for the Pará state, Brazilian Amazon. Salamandra 47 (4): 199-206.
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Natera-Mumaw, Marco; Luis Felipe Esqueda-González & Manuel Castelaín-Fernández 2015. Atlas Serpientes de Venezuela Santiago de Chile, Dimacofi Negocios Avanzados S.A., 456 pp.
Neto, Antonio Mollo; Paola María Sánchez-Martínez and Renato Augusto Junqueira Gaiga 2013. Predation on the lizard Iguana iguana (Sauria: Iguanidae) by the snake Siphlophis compressus (Serpentes: Dipsadidae), at Rondônia state, Brazil. Herpetology Notes 6: 37-38.
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Black Cribo or Mussurana, Clelia clelia (Family Dipsadidae)

By Geoff Gallice (https://www.flickr.com/photos/dejeuxx/) -  https://www.flickr.com/photos/dejeuxx/8707497983/in/set-72157631616756321, CC BY 2.0, https://commons.wikimedia.org/w/index.php?curid=36616142

















Coluber clelia Daudin 1803: 330
Brachyruton cloelia — Duméril, Bibron & Duméril 1854: 1007
Oxyrhopus clelia — Cope 1878: 33
Oxyrhopus cloelia — Garman 1884: 19
Pseudoboa cloelia - Serié 1921
Clelia clelia clelia - Dunn 1944
Clelia clelia groomei Greer 1965
Size: 1.5 m, exceeds 2 meters; hatchlings 230 mm; tail 24% of SVL.

Distribution. Currently considered a widespread species in Central America fro Honduras southward to Panama and into South America as far south as northeast Argentina. 

 Identification: Black with white belly, 19 scale rows at mid-body, reduced to 17 rows in front of the vent, a single anal plate, and divided subcaudal scales. Juveniles have a black head, a white or yellow collar and a red body with each scale containing a black spot. Perhaps most easily confused with its close relative Pseudoboa neuwiedii which has the juvenile coloration seen in this species. But Pseudoboa has single subcaudal scales, and another close relative Oxyrhopus petola which can be solid black has a loreal scale that is about as wide as it is long; Clelia's loreal scale is greatly elongated. Rostral visible from above; nasal divided; one preocular, loreal present in two Trinidad specimens (maybe absent); two postoculars; seven upper labials; six to eight lower labials; ventrals 218−225; cloacal plate single; 62−76  paired subcaudals. Dorsal scales smooth. 

 Habitat: Terrestrial, inhabits forests and savannas, often near water.Biology:  Nocturnal. Diet: almost exclusively ectotherms, subdued with a combination of venom and constriction; includes: Ameiva, Boa, Bothrops, Corallus, and Spilotes. Mammals may also be eaten, including opossums. Eggs number 16−40. Other common names: Vidua, Black cribo, Cribo, Mustarungua, Vidue.

Friday, June 24, 2016

Checkered-bellied Snake, Siphlophis cervinus (Family Dipsadidae)

Coronella cervina Laurenti 1768: 88.

Siphlophis cervinus cervinus — Beebe 1946: 42.


Ranges from Panama, Colombia, Venezuela and Trinidad eastward to the Guianas and Brazil and southward to Bolivia and Peru. A poorly known, highly secretive, nocturnal snake that specializes in feeding on lizards. Size: 634 mm SVL, 173 mm tail; tail 27−32% of the SVL; maximum TL 1.3 m. A very distinctive serpent with a wide head and slender body, a pink to red vertebral stripe, with yellow and black bars on the sides of the body. Rostral visible from above with rounded edge; nasals single; elongate, single loreal; one preocular; two postoculars; 7–9 upper labials; 8–9 lower labial, fourth and fifth enlarged; 240–273 ventrals; anal plate single; 97–116 paired subcaudals. Smooth dorsal scales in 19 rows at mid-body, reduced to 15–17 posteriorly. Dorsum pink to red; head and nape red scales with black-edges; black collar present; black bars, spots, or chevrons distributed over the dorsum and separated by yellow or white with scales that are black tipped; venter and first and second scale rows yellow or white with black spots or bars, giving the underside a checkered appearance. Arboreal in forest and forest-edge habitats. Known to produce clutches of 3-6 eggs.

Black-headed Snake, Tantilla melanocephala (Family Colubridae)

Wilson and Mena (1980) state that Tantilla melanocephala has the widest range of any species in the genus, occurring from Guatemala south to southern Peru, Bolivia, northern Argentina, and Uruguay. They also note it inhabits a wide range of habitats. They write, “Tantilla melanocephala is a widely-distributed snake and, as such, shows a wide range of variation in pattern and scale characteristics. What follows is a summary of those characteristics: (1) head cap cream to dark brown, usually pale brown to dark brown; (2) pale nuchal collar complete, divided medially, divided medially and laterally or reduced to two small spots centered on the parietals (usually not complete); (3) dorsal ground color tan to brown; (4) dark subocular blotch completely separating pre- and postocular pale spots or not; (5) lateral extension of dark head cap present or not; (6) brown to dark brown dark nape band present or not; (7) pale neck band following dark nape band present or not, if present, occupying '/2-2 dorsal scale lengths, sometimes reduced to small spots on either side of the dark middorsal stripe; (8) pale lateral band present or not, if present, usually occupying from as little as the upper portion of row 3 to as much as the upper portion of row 3, all of row 4, and the lower portion of row 5, bounded above and/or below with dark pigment or not. Variation in scales may be summarized as follows: prefrontal in contact with second supralabial on one or both sides or not (in contact on both sides in 66.2% of specimens); first pair of infralabials in contact medially or not (in contact in 80.7% of specimens); ventrals in males 125-174, in females 134-177; subcaudals in males 41-92, in females 41-75. Total length in snakes of all ages ranges from 95-486 mm and tail length ranges from 15-140 mm. Relative tail length ranges from 15.8-35.9%. Range. —From near sea level to intermediate elevations along both versants from Guatemala throughout the length of Central America into South America as far south as southern Peru, Bolivia, northern Argentina, and Uruguay; also on the islands of Trinidad and Tobago.”




Writing about variation in ventrals in the West Indies they state, “Trinidad is 18 to 19 kilometres from the nearest point on the mainland of Venezuela in the north and = 13 kilometres in the south (across the delta of the Orinoco River) and Tobago is 28 to 29 kilometres from the nearest point on Trinidad (near Toco). The differences in ventral counts between specimens from Trinidad and adjacent Venezuela, compared to specimens from Trinidad and Tobago, are striking. Mean ventral numbers in Trinidad are lower by approximately 8 to 15 scales than specimens from adjacent Venezuela. On Tobago, ventral numbers again increase markedly over those in Trinidad and are even higher than those from mainland Venezuela. In fact, only specimens from upper Central America have higher ventrals than those of specimens from Tobago. The mean for ventrals for Trinidad males is 20.2 scales lower than that for Tobagan males. Comparable figures for females are not available, but the count for the single Tobagan female is 9 scales above the highest count for Trinidad females. Ventral numbers decrease in the Guianas (material available only from Guyana and Surinam) as compared to adjacent areas in Venezuela, as well as in Brazil, Uruguay and Paraguay, but increase again in Argentina (the pattern in the latter 4 countries is poorly understood due to the paucity of material).”

Thus, it seems highly unlikely that Tantilla melanocephala is a single, widespread species. The ventral counts given by Wilson and Mena for Trinidad (137- 152 in males and 147-159 in females) do not even overlap with their numbers for Tobago (157-160 for males and 168 for a single female).

Beach Runner, Cnemidophorus lemniscatus (Family Teiidae)




Lacerta lemniscata Linnaeus 1758: 209

Cnemidophorus lemniscatus — Duméril & Bibron 1839: 129.

Other common names: striped runner, foot-shaker.

Size: 91 (34−91) mm male SVL; 63 (47−75) mm female; tails are 2.1−2.2 times the SVL. Identification: A bright green and yellow striped lizard with spots; head longer than broad; narrow snout rounded from above and in profile; rostral pentagonal; nostrils lateral, nasal scales extend dorsally behind rostral and make contact on the midline; frontonasals scales are hexagonal; the frontoparietals are quadrangular and meet on the midline; supraoculars 4−7, separated from 5−7 supraciliaries by one or two rows of granular scales; suboculars 3−5; preoculars absent; postoculars form a row of 3−4 small scales; ear opening large, tympanum visible. Dorsal and lateral scales are granular; ventral scales smooth, rectangular; in eight longitudinal rows and about 30 transverse rows. Most easily confused with Ameiva atrigularis, but that species has 10 longitudinal rows of ventral plates, and attains a larger Size: Smooth ventral scales distinguishing it from Kentropyx, which has 14 transverse rows of keeled ventral scales. Ten light dorsolateral stripes 3−4 scale rows wide, each separated by a dark stripe 5−9 scales wide. Scales around midbody 123 and 124 in two specimens; ventral scales 29 and 31 transverse rows in two specimens. Anterior dorsal surface of front legs covered with plate-like scales that overlap; granular scales cover the rest of the legs. Hind legs with overlapping plate-like scales on the anterior and ventral surfaces, granular scales dorsally and posteriorly. Scales on tail quadrangular, overlapping and keeled. Fingers compressed with 15−17 lamellae on fourth digit; toes compressed with 30−33 lamellae on fourth digit. Live females have a brown back with white stripes and dorsolateral stripes are green on the anterior; anterior venter of females is white, posteriorly it is green-yellow; females also have a brown tail. Males have lateral stripes that are replaced by 2−3 rows of white spots, posteriorly the dorsolateral region is blue-green, and the tail is blue. Both sexes have the ventral surface of the tail colored blue or green.

Distribution: A disjunct distribution from Central America to northern Brazil, including Trinidad (including Chacachacare and Huevos islands), Tobago, Little Tobago; present on some islands off north central Venezuela, west of Trinidad & Tobago. It has been introduced into Florida. C. lemniscatus is a species complex containing several cryptic and sibling species and clones. The Trinidad and Tobago populations are bisexual.

Habitat: A beach-savanna lizard that will enter forest and colonize open sunny areas; forage on open ground using bushy areas for shelter; abundant along Manzanilla Bay Beach and at Icacos Beach; use burrows for shelter, one burrow examined was 17−20 cm in depth.

Biology: Diurnal. Diet: Arthropods, mostly insects but also earthworms, flowers of Portulaca. Predators. hawks, the snake Oxybelis aeneus, and the tegu lizard, Tupinambis. Ameiva will chase Cnemidophorus, this may be attempted predation, or competition for territory. Cnemidophorus stop abruptly between spurts of rapid, often bipedal, locomotion; they will lift one of their front legs and vibrate or wave their feet; this may represent a territorial display, or have other social significance.

Long-tailed Machete Savane, Chironius (Macrops) septentrionalis (Family Colubridae)

Chironius multiventris septentrionalis Dixon, Wiest & Cei 1993: 173.
Chironius septentrionalis — Hollis 2006:445.

Size. Males to 1.1 m SVL, total length 1.8 m. Females to 1.2 m SVL, total length of 1.9 m. Diagnosis. This gracile, olive green species is morphologically cryptic with C. carinatus. However, this species has a higher ventral count (161–174) and subcaudal count (161–179) as well as a proportionally longer tail than C. carinatus. 

Distribution is restricted to the Caribbean Coastal Range of northern Venezuela and Trinidad. All of the Trinidad specimens are from the Northern Range, and its foothills. Life History inhabits lowland areas, probably using forests and forest edge habitats, it is diurnal. Diet is mostly on frogs. Reproduction. Females reported with clutches of 2–4 eggs.

Monday, May 23, 2016

Marine Toad, Rhinella marina (Family Bufonidae)

The marine toad, locally known as crapaud, can be found throughout Trinidad and Tobago as it occurs in a variety of terrestrial habitats from urban areas, agricultural lands to forests. It may be considered the largest toad in the world with a maximum size of 238 mm SVL, with females larger than males. This species is known to feed on anything it can swallow. It can be distinguished from the Beebe's toad also found on Trinidad & Tobago by the position of its nostrils and its heavily webbed hind feet. It has toxic chemicals in its skin that can result in fatality if consumed.

Marine Toad, Cane Toad

Rhinella marina (Linnaeus, 1758)


Rana marinaLinnaeus, 1758, Syst. Nat., Ed. 10, 1: 211. Type(s): By indication including specimen illustrated in Seba, 1734, Locuplet. Rer. Nat. Thesaur. Descript. Icon. Exp. Univ. Phys. Hist., Type locality: "America"; restricted by Müller and Hellmich, 1936, Wissenschaft. Ergebn. Deutschen Gran Chaco Exped., Amph. Rept.: 14, to Surinam.

Bufo marinus — Schneider, 1799, Hist. Amph. Nat.: 219.

Chaunus marinus — Frost, et al. 2006, Bull. Am. Mus. Nat. Hist., 297: 364.

Rhinella marina — Chaparro, Pramuk, and Gluesenkamp, 2007, Herpetologica, 63: 211.


Distribution. Marine toads (Rhinella marina) occur naturally from southern Texas and Sonora and Tamaulipas Mexico southward to the Orinoco and Amazon River Basins of South America. They have been introduced over much of the tropical world to control agriculture pests to most tropical regions as a control for agricultural pests. They occur naturally in Trinidad and Tobago.

Marine toads, or crapauds as they are known in the islands, use shallow bodies of clear water with a high pH and minimal vegetation to reproduce. The breeding sites may be in shallow brackish waters in coastal areas or they may use pools in streams running through agricultural areas or forests. Man-made bodies of water such as concrete ponds, old foundations that collect water, abandoned swimming pools, or natural ponds in forests or forest edge situations.

The marine toad is so prevalent in Trinidad and Tobago that it has taken on a cultural role, albeit a superficial one. While Amerindians may have lived on the islands for thousands of years, Trinidad and Tobago were not discovered by the European world until Christopher Columbus' third voyage in 1498. And, early European colonization was slow. Trinidad's human population probably numbered in the hundreds until 1785, and Tobago's population was similarly small. Thus these islands have only been inhabited with substantial populations of Africans and Europeans for less than 300 years.
The toad's local name, "crapaud," is French for "toad," and in Speyside, Tobago there is a street named after this largest native amphibian. The marine toad has also become part of local culture and colloquialisms. Tobagonians wishing to silence a hostile witness in court will attempt to intimidate the witness by sewing a crapaud's mouth shut and placing it in the witness' house the night before the trial. Also, in predicting misfortune or offering a warning the phrase, "Crapaud smoke your pipe!" may be used (Niddrie, 1980). As we will see the crapaud has taken on a more complex role in other cultures.

The marine toad was one of the first (actually the eighth) amphibians to be described by science. Carl Linneaus, the Swedish founder of the current binomial nomenclatural system used by biologists, named and described the giant toad, "Rana marina" on page 211 of his first volume of Systema naturae... in 1758. Sixteen years later John Julius Walbaum proposed that Linnaeus' name for this toad was inappropriate. Walbaum (1784) (in Smith et al. 1977) wrote,

I seriously doubt that it usually lives in the ocean, because the structure of the feet is not such that it would be able to swim with them through the rough waves of the ocean. therefore I assume it to be a land frog which lives at the banks of rivers or shores of lakes. If this assumption is confirmed in the future, the Latin specific name applied by Linnaeus would have to be changed because it does not correctly characterize the species.

Wallbaum's proposal is not acceptable today because Article 18(a) of the International Code of Zoological Nomenclature makes it clear that a genus, or a species-group name, cannot be changed once it is established, even if it is inappropriate. But, a species may be moved from one genus to another. Linnaeus recognized only 10 genera of amphibians and reptiles in his 1758 work. Joseph Nicolaus Laurenti was the next person to review amphibian and reptile classification, and he established the genus Bufo in 1768. Today, Article 34(b) of the International Code requires that changes in species names must made so that they agree with the gender of the genus. Thus, Rana marina is feminine, while Bufo is masculine. When marinus was moved to Bufo, it therefore became Bufo marinus. When the species was re-assigned to the genus Rhinella, it again became feminine and today it is known as Rhinella marina.

There are competing species for the honor of the largest toad. However, the largest toad species appears to be South American, and the contest for the largest species is between Blomberg's toad, Rhaebo blombergi, and the marine toad. Blair (1972) and Duellman and Trueb (1986) considered Blomberg's toad of Colombia the largest toad species, the latter authors give its length as 250 mm. Reed and Borowsky (1970) reported five female marinus ranging from 208-230 mm, all are museum specimens, and all are from Suriname and Guyana. A newspaper article (Anon., 1988) reported the death of a marine toad at the Blank Park Zoo, in Des Moines, Iowa. This animal, named "Totally Awesome," or Toad A, weighed 5 pounds 1.5 ounces (2.3 kg), and was 9.5 inches (241.3 mm) in total length. It was accepted into the Guinness Book of World Records (McFarland, 1991) as the largest toad. The zoo obtained the toad from a Miami animal dealer in 1983, thus the toad's exact age was unknown. A similarly sized specimen was reported by Tyler (1994), the specimen is currently in the Queensland Museum, and it measured 24.1 cm, and weighed (presumably when it was alive) 1.36 kg. Other toad species in the marinus Group also attain respectable sizes, Cei (1980) reported the maximum size of the kurúrú guazú (also spelled cururú), Bufo paracnemis as 210 mm in length. North American's largest toad is the Colorado River toad, Incilius alvarius, Stebbins (1985) described I. alvarius reaching 190 mm in body length. Asia also has toads that reach impressive lengths. As Boring and Lui (1934) pointed out, most continents have at least one toad species that reaches a large size.

The habitat used by Rhinella marina may have an impact on the size they reach. The largest specimens of Rhinella marina on Trinidad appear to come from the Northern Range. While the breeding population in Nariva is much smaller. This may be the result of completion for breeding sites. Shallow bodies of water are few in the Northern Range while breeding sites in Nariva Swamp are exceptionally common.

Breeding activity in Trinidad and Tobago coincides with the wet season which may start in May and continue until December or January. However, much of the activity occurs in the early and middle wet season in June and July. Males will call well after breeding has ceased.

Eggs are deposited in both permanent and ephemeral situations, the crapaud tends to prefer bodies of water with abundant aquatic plants and a neutral pH. One a female has selected a mate, they may remain in amplexus for a long period (up to two weeks). Clutch sizes of 4,000 to 36,000 have been reported, with larger females laying more eggs. Experiments with desiccating eggs fond the larvae could survive 10 hours without water as long as the surface was moist. Tadpoles emerge 48–72 hours after deposition. Tadpoles usually metamorphose 27–46 (however a range of 10–180 days has been reported). This may result from temperature differences of the water.

Marine Toad tadpoles feed on algae and other aquatic detritus (Hinckley, 1962) and its availability affects the time to metamorphosis (Tyler, 1975).

Tadpoles prefer warmer water and are adapted to high water temperatures, and are often exposed with little or no vegetative cover beside or in the water body. Tadpoles remain active throughout their development and swim in large aggregations mid water column (Straughan 1966; Krakauer 1970). Tadpoles may be cannibalistic and feed on individuals that are younger and smaller than they are, and they apparently tend to feed just on other Marine Toad tads, and not other species of anurans (Crossland, 1998a).

New metamorphosed and post-metamorphic toads remain near water because they can easily desiccate (Straughan, 1966; Alford et al., 1995a). As toads get older and larger they move farther from water and they shift their daily activity from diurnal to nocturnal behavior. Juveniles in the 30–70 mm emerge at dusk and are active at night—they are frequently found under lights, feeding on the insects attracted to the light (Krakauer, 1968).

Adults are tolerant and even thrive in human modified environments. They occur in gardens, around houses, and in water tanks (Wright and Wright, 1949). Krakauer (1968, 1970) notes that marine toads are frequently found in disturbed areas and rarely encountered in undisturbed habitats. Marine toads are nocturnal and attracted to house and patio lights that also attract the insects on which toads feed (Wright and Wright, 1949). Toads are only active 1 out of every three to five nights (Brattstrom, 1962a; Zug and Zug, 1979; Floyd and Benbow, 1984), and their activity tends to be correlated with rain (Floyd and Benbow, 1984). During the day they hide under debris on the ground and in burrows (Wright and Wright, 1949), and under long grass clumps out of direct sunlight (Cohen and Williams, 1992).

As their name suggests, marine toads are generally found along rivers and coasts in association with fresh and/or brackish water, including mangrove swamps. In a study by Krakauer (1970), adult toads were found to survive in 10‰ sea water, but quickly died in 15‰ sea water. We have observed this toad emerging from the surf along turtle nesting beaches in Trinidad, probably individuals that got washed down stream during heavy rains and followed the coast for a short distance until they could return to land.

Home range size is variable, dependent to an extent on the size of their water bodies and feeding sites (Brattstrom, 1962a; Carpenter and Gillingham, 1987). Displaced animals will return to their capture site using local landscape and visual cues providing the key inputs for orientation (Brattstrom, 1962a). Mark and recapture studies In Queensland, Australia, and the average minimum home range was calculated at 340 m2 (Pearse, 1979). A similar study by Zug and Zug (1979) found that at least some toads were familiar with an area of 2,812 m2.

Marine toads do not defend territories during the reproductive season at the breeding site or in their foraging area (Sabath, 1980). Adult toads do display some fidelity to shelter sites and prefer shelters with high soil moisture, and often increase soil moisture by urinating on the soil (Alford et al., 1995a).

Toads are able to reproduce at body lengths of 66–220 mm, with males averaging about 13 mm shorter than females (Wright and Wright, 1949; Easteal, 1986).

Marine toads feed on a wide variety of terrestrial arthropods. However, they will consume native frogs and toads, dog food, and feces (Alexander, 1964; Tyler, 1975; Rossi, 1983; Bartlett and Bartlett, 1999a). Other prey include snakes (Rabor, 1952), birds (Krakauer, 1968), and mammals (Oliver, 1949).

Noxious and toxic chemicals in the skin and tissues at all points in the toad’s life cycle keep the possible predators few in number. At the tadpole stage, dragonfly naiads will readily consume marine toad tadpoles and eggs, as will dytiscid beetles, water scorpions (Lethocerus sp.), notonectids (Anisops sp.), leeches, tortoises, Macrobrachium spp., and crayfish (Cherax quadricarinatus; Crossland, 1992, 1993; Alford et al., 1995a). Native fishes have been found to ignore or taste and reject toad tadpoles (Alford et al., 1995a; Lawler and Hero, 1997). The most frequent predators of toad eggs and tadpoles, however, are older cohorts of marine toad tadpoles (Alford et al., 1995b).

Toads are most vulnerable to predation immediately following metamorphosis, while the development of terrestrial skin glands is occurring (Cohen and Alford, 1993). Although there are no studies on predators of newly metamorphosed toads, several animals have been observed to eat them, including adult marine toads, ants, centipedes, wolf spiders, small mammals, and some birds (Cohen and Alford, 1993).

Marine toads are highly poisonous and secrete a whitish, viscous compound from their parotoid glands (in Wright and Wright, 1949; Allen and Neill, 1956; Licht, 1967b; Easteal, 1986). The parotoid glands produce and store a mixture of bufotenine and epinephrine—steroid-like substances that are toxic to most animals (Chen and Osuch, 1969; Freeland, 1986). When confronted by a predator the toad goes into a head-down defensive position marine toads assume to present their parotoid glands to potential predators. These toads are known to approach potential predators and attempt to force contact with their parotoid glands.

The oldest fossil of marinus is known from a floodplain deposit in the late Miocene (5.3-11.2 MYA) of Colombia (Estes and Wasserzug, 1963). Estes and Wasserzug considered marinus the most primitive member of the species group, and suggested it gave rise to populations adapted for life in wet and dry environments on mainland South America. Bertini and Cei (1962) suggested Rhinella marina had an Amazonian origin, later Cei (1972) hypothesized the Guiana shield was marinus' point of origin.


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