Of the six species of Anolis, all except A. sericeus are typically found in humid forests. Anolis sericeus sericeus is poorly represented in the collections from southern El Petén, where it may be in competition with Anolis limifrons rodriguezi that resembles Anolis s. sericeus in size, coloration, and habits. Therefore, Anolis sericeus sericeus is excluded from the following discussion. The common terrestrial species is Anolis humilis uniformis; sometimes this small species perches or suns on the bases of small trees or buttresses of some large trees. When disturbed it takes to the ground and seeks cover in the leaf litter or beneath logs or palm fronds. Anolis lemurinus bourgeaei is about twice the size of Anolis humilis uniformis and is usually observed on buttresses of large trees or on the lower two meters of tree trunks. Individuals were seen foraging on the ground along with Anolis humilis uniformis. At no time were Anolis lemurinus bourgeaei observed to ascend the trunks of large trees; they always took refuge near the bases of trees. Anolis limifrons rodriguezi is found on the stems and branches of bushes. It is a small species that sometimes is observed on the ground but was never seen ascending large trees. Anolis capito is about the same size as Anolis lemurinus bourgeaei and lives on the trunks of large trees. In the tops of the trees lives a large green species, Anolis biporcatus.
Similar segregation habitatwise can be demonstrated for other members of the herpetofauna. The avoidance of interspecific competition in feeding is well illustrated by three species of snakes that probably are the primary ophidian predators on frogs. Drymobius margaritiferus margaritiferus is diurnal and terrestrial; it feeds on frogs at the edges of breeding ponds by day. Also during the day Leptophis mexicanus mexicanus feeds on frogs in bushes and trees. At night the activities of both of these species is replaced by those of Leptodeira septentrionalis polysticta, which not only feeds on the frogs in the trees and bushes, but descends to the ground and even enters the water in search of food.
From the examples discussed above, the importance of the three dimensional aspect of the rainforest is apparent. The presence of a large and diverse habitat above the ground is of great significance in the rainforest, for of the non-aquatic components of the herpetofauna in the rainforests of southern El Petén, 42 per cent of the species spend at least part of their lives in the bushes and trees. Another important part of the forest is the subterranean level—the rich mulch, underground tunnels, and rotting subterranean vegetation. Of the 78 species of amphibians and reptiles in southern El Petén, seven are primarily fossorial, and half-a-dozen others are secondarily fossorial. Probably the fossorial members of the fauna are the least well represented in the collection, for such widespread species as Dermophis mexicanus mexicanus, Rhadinaea decorata decorata and Tantilla schistosa schistosa were expected, but not found.
In the following discussion of the ecological distribution of amphibians and reptiles in the rainforest I have depended chiefly on my observations made in southern El Petén, but have taken into consideration observations made on the same species in other regions, together with reports from other workers. The reader should keep in mind that the evidence varies from species to species. Of some species I have observed only one animal in the field; of others, I have seen scores and sometimes hundreds of individuals. For species on which I have few observations or rather inconclusive evidence, the circumstance of inadequate data is mentioned.
In analyzing the ecological distribution within the forest, it is convenient to recognize five subdivisions (habitats); each is treated below as a unit.
1. Aquatic.—This habitat includes permanent streams and rivers (Pl. 10, fig. 1), some of which are clear and others muddy. In the rainy season temporary ponds form in depressions on the forest floor (Pl. 10, fig. 2); these are important as breeding sites for many species of amphibians. Aquatic members of the herpetofauna are here considered to be those species that either spend the greatest part of their lives in the water or usually retreat to water for shelter. Seven species of turtles and one crocodilian are aquatic. Of these, Dermatemys mawi, Staurotypus triporcatus, and Pseudemys scripta ornata inhabit clear water, whereas Chelydra rossignoni, Claudius angustatus, Kinosternon acutum, and K. leucostomum inhabit muddy water. Crocodylus moreleti apparently inhabits both clear and muddy water, for in the dry season it lives along the clear rivers, but in the rainy season inhabits flooded areas in the forest as well.
2. Aquatic Margin.—Extensive marshes were lacking in the part of southern El Petén that I visited; consequently, the aquatic margin habitat is there limited to the edges of rivers and borders of temporary ponds. Bufo marinus, Rana palmipes, and Rana pipiens are characteristic inhabitants of the aquatic margin, although in the rainy reason Bufo marinus often is found away from water. Observations indicate that Tretanorhinus nigroluteus lateralis inhabits the margins of ponds and streams and actually spends considerable time in the water. Although Iguana iguana rhinolopha is arboreal, it lives in trees along rivers, into which it plunges upon being disturbed. Species included in this category are those that customarily spend most of their lives at the edge of permanent water. Frogs and toads that migrate to the water for breeding and the snakes that prey on the frogs at that time are not assigned to the aquatic-margin habitat.
3. Fossorial.—Characteristic inhabitants of the mulch on the forest floor are Bolitoglossa moreleti mulleri, Lepidophyma flavimaculatum flavimaculatum, Scincella cherriei cherriei, Ninia sebae sebae, Pliocercus euryzonus aequalis, and Micrurus affinis apiatus. Other species of snakes that spend most of their lives above ground often forage in the mulch layer; among these are Coniophanes bipunctatus biserialis, Coniophanes fissidens fissidens, Coniophanes imperialis clavatus, Lampropeltis doliata polyzona, and Stenorrhina degenhardti. Among the amphibians, at least Hypopachus cuneus nigroreticulatus, Eleutherodactylus rostralis, and Syrrhophus leprus are known to seek shelter in the mulch.
4. Terrestrial.—One turtle, Geoemyda areolata, is primarily terrestrial. Among the lizards, conspicuous terrestrial species are Anolis humilis uniformis and Ameiva festiva edwardsi; Anolis lemurinus bourgeaei and Basiliscus vittatus spend part of their lives on the ground, but also live on trees and in bushes. Eumeces schwartzei and E. sumichrasti apparently are terrestrial. The only terrestrial lizard that is nocturnal is Coleonyx elegans elegans, which by day hides in the leaf litter or below ground. Nocturnal amphibians that are terrestrial include Bufo marinus, Bufo valliceps valliceps, Eleutherodactylus rugulosus rugulosus, Syrrhophus leprus, and Hypopachus cuneus nigroreticulatus. A large number of active diurnal snakes are terrestrial; these include Boa constrictor imperator, Clelia clelia clelia, Dryadophis melanolomus laevis, Drymarchon corais melanurus, Drymobius margaritiferus margaritiferus, Pseustes poecilonotus poecilonotus, and Spilotes pullatus mexicanus. Nocturnal terrestrial snakes include three kinds of Bothrops (B. atrox asper, B. nasutus, and B. nummifer nummifer), all of which seem to be equally active by day.
5. Arboreal.—In this habitat the third dimension (height) of the rainforest probably is the most complex insofar as the inter-relationships of species and ecological niches are concerned. I have attempted to categorize species as to microhabitats within the arboreal habitat; in so doing, I recognize four subdivisions—bushes, tree trunks, tree tops, and epiphytes.