Research Article |
Corresponding author: Ricardo Marques ( rcdmarquess@gmail.com ) Academic editor: Robert Jadin
© 2016 Ricardo Marques, Konrad Mebert, Érica Fonseca, Dennis Rödder, Mirco Solé, Moacir Santos Tinôco.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Marques R, Mebert K, Fonseca É, Rödder D, Solé M, Tinôco MS (2016) Composition and natural history notes of the coastal snake assemblage from Northern Bahia, Brazil. ZooKeys 611: 93-142. https://doi.org/10.3897/zookeys.611.9529
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Information about the snake diversity and their natural history from the Atlantic forest domain in Brazil refer mostly to inland forests than to coastal region. Within the state of Bahia, this knowledge is concentrated to the southeastern coastal stretch. Herein we report on the diversity of snakes from the restinga, ombrophilous forest and anthropogenic environment from the northern Atlantic coast of Bahia. We sampled nine sites for three years and visited four museum collections. Furthermore, we provide anecdotal natural history information, voucher analyses, literature complements, and a key to fascilitate species identification. We report a total of 774 snakes belonging to 50 species and 23 new distribution records for northeastern coast of Bahia, supplemented by new data on feeding and reproduction. The number of detected species is similar to numbers obtained in comparable studies from other Brazilian ecoregions. This study reports and focuses for the first time on all known species of snakes from the northeastern coast of Bahia.
Atlantic forest, coastal sand dunes, conservation, ombrophilous forest, restinga, snakes, conservation
Studies on diversity inventories and natural history increase the knowledge of a regional fauna, its interaction with other organisms, and the environment in general (
As a first step, pertinent and relevant taxa-related information can be acquired through species inventories and studies describing aspects of natural history that increase our knowledge on the different habitats and habits of regional snakes (
Studies involving snakes from northeastern Brazil are often species inventories from the Caatinga and transition areas with other ecoregions (
The present study was conducted on the northern coast of Bahia, which extends for 220 km from Salvador to the boundaries of the state of Sergipe (Figure
a) Fieldwork
Snakes were sampled during 18 bimonthly fieldtrips from 2010 to 2013, covering three dry seasons and three rainy seasons, totaling in 162 field days. We sampled eight coastal sites of the restinga ecosystem: Busca Vida (-12.8619 S, -38.2708 W), Arembepe (-12.7236 S, -38.1416 W), Praia do Forte (-12.5748 S, -38.0147 W), Imbassaí (-12.4791 S, -37.9602 W), Massarandupió (-12.3172 S, -37.8404 W), Baixio (-12.1123 S, -37.7062 W), Barra do Itariri (-11.9478 S, -37.6113 W) and Costa Azul (-12 S, -37.496 W); and the Instituto da Mata, an ombrophilous forest fragment of 410 ha at 20 km from coast (-12.450073 S, -38.234579 W). Surveys were authorized under ICMBio No 23355-2.
Four sampling sources were used to acquire data on snakes: (1) Visual Encounter Survey (VES) limited by time, i.e. recording visually detected and manually captured snakes; (2) dead specimens found by locals; (3) carcasses and shed skins detected by us; and (4) incidentally encountered and recorded snakes outside the VES. For the VES, we walked for two hours on four 500 m transects placed on four aforementioned vegetation types. The VES covered the period from 06:00 h and 18:00 h in six turns: 06:00–08:00; 08:00–10:00; 10:00–12:00; 12:00–14:00; 14:00–16:00; 16:00–18:00. In the last year VES was performed during nighttime from 19:00 h to 21:00 h at Busca Vida, Baixio, Barra do Itariri and Instituto da Mata, totaling a sample effort of 3024 h (2592 h diurnal and 432 h nocturnal). During the VES and incidental encounters we recorded for each snake the time of activity, predominant vegetation type and microhabitat. Each captured snake was marked and then released at its site of capture. Marking involved fluorescent elastomer applied subcutaneously in the ventral scales. The ith number of the ventral scale, with the first number being the ventral scale anterior the anal plate, corresponding to the ith number of the captured snake (adapted from
b) Animal characterization
All species were identified according to the literature (
Snout-Vent Length (SVL) and sex was recorded from all captured animals and museum specimens when possible. We observed predation events, and during the last year of surveys, we forced animals to regurgitate their stomach content through manual palpation.
Morphological characteristics of the animals from the region comprising scale counts, body shape and coloration allowed us to elaborate an identification key to all species recorded in this study. We complemented the information of animals with records obtained from the literature, as well as field observations and data from voucher specimens. We did not include natural history notes of introduced (non-native) species.
c) Data collection in museums
Specimens of four scientific collections from the state of Bahia were analysed: Museu de Zoologia at
Species richness and frequency were computed based on the species sampled during fieldwork only, excluding specimens housed in collections. The frequency of the species from the northern coast of Bahia followed the model adapted by
A total of 194 snakes were recorded during fieldwork and 580 obtained from museum collections, totaling 774 snakes of a total of 49 native species. Of those, 32 species were recorded during fieldwork and 17 species were complemented through museum records and literature references. Twenty-three new distributional records of species are added for the northern coastal stretch of Bahia (see Table
Snake species from the northern coast of Bahia. Number of specimens from fieldwork (N), frequency (f%), dominance (D%) and number of specimens from museum specimens (NC). New records (*); Introduced species (**); Extracted from
Species | N | f% | D% | NC |
---|---|---|---|---|
Infraorder Scolecophidia Cope, 1864 | - | - | - | - |
Typhlopidae Merrem, 1820 | - | - | - | - |
Amerotyphlops brongersmianus (Vanzolini, 1976)* | 1 | 5.55 | 0.51 | 6 |
Infraorder Henophidia Nopcsa, 1923 | ||||
Boidae Gray, 1825 | ||||
Boinae Gray, 1825 | ||||
Boa constrictor constrictor Linnaeus, 1758 | 19 | 72.22 | 9.79 | 4 |
Corallus hortulanus (Linnaeus, 1758) | 1 | 5.55 | 0.51 | - |
Epicrates assisi Machado, 1945* | - | - | - | 1 |
Eunectes murinus (Linnaeus, 1758) | 3 | 16.67 | 1.54 | 2 |
Caenophidia Hoffstetter, 1939 | ||||
Colubridae Oppel, 1811 | ||||
Chironius bicarinatus (Wied, 1820)*** | - | - | - | - |
Chironius carinatus (Linnaeus, 1758)* | 2 | 11.1 | 1.03 | - |
Chironius exoletus (Linnaeus, 1758) | 1 | 5.55 | 0.51 | 13 |
Chironius flavolineatus (Jan, 1863) | 22 | 72.22 | 11.34 | 16 |
Drymarchon corais corais (Boie, 1827)* | - | - | 0.51 | 2 |
Drymoluber dichrous (Peters, 1863)* | - | - | 0.51 | 4 |
Leptophis ahaetulla liocercus (Wied, 1824)* | 1 | 5.55 | 0.51 | 3 |
Mastigodryas bifossatus (Raddi, 1820)* | - | - | - | 4 |
Oxybelis aeneus (Wagler, 1824) | 6 | 22.22 | 3.09 | 5 |
Pantherophis guttatus (Linnaeus, 1766)** | - | - | - | 1 |
Spilotes pullatus pullatus (Linnaeus, 1758) | 2 | 11.11 | 1.03 | 7 |
Spilotes sulphureus sulphureus (Wagler, 1824) | 1 | 5.55 | 0.51 | - |
Tantilla melanocephala (Linnaeus, 1758)* | 2 | 11.11 | 1.03 | 9 |
Dipsadidae Bonaparte, 1838 | ||||
Dipsadinae Bonaparte, 1838 | ||||
Dipsadini Bonaparte, 1838 | ||||
Sibynomorphus neuwiedi (Ihering, 1911) | 2 | 11.11 | 1.03 | 13 |
Imantodini Myers, 2011 | ||||
Imantodes cenchoa cenchoa (Linnaeus, 1758) | 1 | 5.55 | 0.51 | 1 |
Leptodeira annulata annulata (Linnaeus, 1758)* | 5 | 22.22 | 2.57 | 21 |
Xenodontinae Bonaparte, 1845 | ||||
Echinantherini Zaher, Grazziotin, Cadle, Murphy, Moura-Leite & Bonatto, 2009 | ||||
Taeniophallus occipitalis (Jan, 1863) | 5 | 27.78 | 2.57 | 4 |
Hydropsini Dowling, 1975 | ||||
Helicops angulatus (Linnaeus, 1758)* | 11 | 27.78 | 5.67 | 10 |
Helicops leopardinus (Schlegel, 1837)* | 1 | 5.55 | 0.51 | 14 |
Philodryadini Cope, 1886 | ||||
Philodryas nattereri Steindachner, 1870 | 38 | 83.33 | 19.58 | 11 |
Philodryas olfersii herbeus Wied, 1825 | 9 | 33.33 | 4.63 | 13 |
Philodryas patagoniensis (Girard, 1858) | 14 | 50 | 7.21 | 18 |
Pseudoboini Bailey, 1967 | ||||
Clelia plumbea (Wied, 1820)* | - | - | - | 3 |
Oxyrhopus petolarius digitalis Reuss, 1834* | 2 | 11.11 | 1.03 | 3 |
Oxyrhopus trigeminus Duméril, Bibron & Duméril, 1854 | 9 | 33.33 | 4.63 | 46 |
Phimophis guerini (Duméril, Bibron & Duméril, 1854) | - | - | - | 4 |
Pseudoboa nigra (Duméril, Bibron & Duméril, 1854)* | - | - | - | 7 |
Siphlophis compressus (Daudin, 1803) | 1 | 5.55 | 0.51 | - |
Thachymenini Bailey, 1967 | ||||
Thamnodynastes pallidus (Linnaeus, 1758) | 1 | 5.55 | 0.51 | - |
Xenodontini Bonaparte, 1845 | ||||
Erythrolamprus aesculapii venustissimus Wied, 1821* | - | - | - | 1 |
Erythrolamprus almadensis (Wagler, 1824)* | 2 | 11.11 | 1.03 | 17 |
Erythrolamprus miliaris merremi (Wied, 1821)* | - | - | - | 3 |
Erythrolamprus poecilogyrus schotti (Schlegel, 1837)* | - | - | - | 21 |
Erythrolamprus reginae semilineatus (Wagler, 1824) | 1 | 5.55 | 0.51 | 8 |
Erythrolamprus taeniogaster (Jan, 1863) | 1 | 5.55 | 0.51 | 12 |
Erythrolamprus viridis viridis (Günther, 1862)* | - | - | - | 1 |
Xenodon merremii (Wagler, 1824)* | 1 | 5.55 | 0.51 | 23 |
Xenodon rabdocephalus rabdocephalus (Wied, 1824)* | - | - | - | 2 |
Elapidae Boie, 1827 | ||||
Elapinae Boie, 1827 | ||||
Micrurus corallinus (Merrem, 1820)* | - | - | - | 1 |
Micrurus ibiboboca (Merrem, 1820) | 16 | 55.56 | 8.24 | 81 |
Viperidae Laurenti, 1768 | ||||
Crotalinae Oppel, 1811 | ||||
Bothrops erythromelas Amaral, 1923 | - | - | - | 2 |
Bothrops leucurus Wagler, 1824 | 10 | 44.44 | 5.15 | 146 |
Bothrops lutzi (Miranda-Ribeiro, 1915) | - | - | - | 3 |
Crotalus durissus cascavella Wagler, 1824 | 3 | 16.67 | 1.54 | 13 |
Lachesis muta rhombeata Wied-Neuwied, 1824* | - | - | - | 1 |
Total number of specimens | 194 | - | 100% | 580 |
The most diverse family was Dipsadidae (25 spp.), representing 50% of the records. The second most diverse family was Colubridae (13 spp.), followed by Viperidae (5 spp.), Boidae (4 spp.), Elapidae (2 spp.) and Typhlopidae (1 sp.). Among the recorded species Philodryas nattereri (n = 38), Chironius flavolineatus (n = 22) and Boa constrictor (n = 19) were the most frequent species in restinga habitat, whereas Helicops angulatus (n = 11) dominated ombrophilous forest edges.
Epicrates assisi, Drymarchon corais corais, Drymoluber dichrous, Mastigodryas bifossatus, Clelia plumbea, Phimophis guerini, Pseudoboa nigra, Erythrolamprus aesculapii venustissimus, E. miliaris merremii, E. poecilogyrus schotti, E. viridis viridis, Xenodon rhabdocephalus rhabdocephalus, Micrurus corallinus, Bothrops erythromelas, B. lutzi and Lachesis muta rhombeata were detected only through museum vouchers, and appear to be rare (n ≤ 4), except for E. p. schotti (n = 21) and P. nigra (n = 7).
Diurnal activity was recorded for 158 snakes during all surveys with members of the families Typhlopidae, Colubridae (except T. melanocephala) and Elapidae restricted to diurnal activity. Our observations show snakes were mostly active during morning between 08:00 h and 11:59 h and less frequently observed during the afternoon (Figure
Stomach contents of 11 species were analysed. Lizards represented 40% of food items, followed by amphibians (20%), mammals and snakes (15% each), fishes and invertebrates (5% each). The lizard Ameivula ocellifera was the most recurrent prey item in restinga with observed predatory events between 09:50 h and 13:06 h. Two isolated events of Oxyrhopus trigeminus feeding on A. ocellifera were recorded, when the snakes (SVL = 320 mm and 315 mm) preyed on three lizards (SVL = 53.8 mm and 51.9 mm; a partially digested specimen, respectively). Another lizard species ingested by O. trigeminus was Tropidurus hygomi. In addition, A. ocellifera was also a food item of Philodryas nattereri in two different events. In the first, the snake (SVL = 390 mm) regurgitated a partially digested A. ocellifera. In the second event, an adult P. nattereri subdued the lizard and disappeared immediately thereafter with it. We report the first predatory event of the alien species Hemidactylus mabouia (SVL = 41.5 mm) by Chironius flavolineatus (SVL = 610 mm). The viper B. leucurus collected in a nearby anthropogenic construction site at the Instituto da Mata contained T. hispidus remnants in its stomach.
Amphibians were the second most frequent food item. An unidentified tadpole (total lenght = 39.4 mm) was ingested by a juvenile Chironius exoletus (SVL = 190 mm). We recorded the ingestion of Leptodactylus natalensis by Helicops angulatus in two events, both partially digested. One of these events also revealed frog eggs, possibly of the same prey species. Herein we report the first predation record of Amerotyphlops brongersmianus (SVL = 321.1 mm) by Micrurus ibiboboca (SVL = 558 mm) and the first cannibalism event of O. trigeminus in which a specimen (SVL = 390 mm) ingested a juvenile (SVL approximately 140 mm). We list all food items and new predatory records in Table
Stomach content of snake from the northern coast of Bahia, number of items found by species (N). New records for this species’ diet (*).
Species | N | Food item |
---|---|---|
Colubridae | ||
Chironius flavolineatus | 1 | Hemidactylus mabouia (Squamata, Gekkonidae)* |
Chironius exoletus | 1 | Tadpole |
Dipsadidae | ||
Sibynomorphus neuwiedi | 1 | Gastropod (Mollusca, Veronicellidae) |
Helicops angulatus | 2 | Leptodactylus natalensis (Anura, Leptodactylidae)* |
1 | Anuran eggs | |
Helicops leopardinus | 1 | Geophagus brasiliensis (Pisces, Cichlidae) |
Oxyrhopus trigeminus | 1 | Tropidurus hygomi (Squamata, Tropiduridae)* |
3 | Ameivula ocellifera (Squamata, Teiidae) | |
1 | Oxyrhopus trigeminus (Serpentes, Dipsadidae)* | |
Philodryas nattereri | 2 | Ameivula ocellifera (Squamata, Teiidae) |
Philodryas patagoniensis | 1 | Philodryas olfersii (Serpentes, Dipsadidae) |
Elapidae | ||
Micrurus ibiboboca | 1 | Amerotyphlops brongersmianus (Serpentes, Typhlopidae)* |
Viperidae | ||
Bothrops leucurus | 1 | Tropidurus hispidus (Squamata, Tropiduridae) |
2 | Rattus norvegicus (Mammalia, Muridae) | |
Crotalus durissus | 1 | Rattus sp. (Mammalia, Muridae) |
Amerotyphlops brongersmianus Vanzolini, 1976
Fig.
A rare species, small sized (min SVL = 110 mm, max SVL = 315 mm). Recorded at Reserva Sapiranga, Imbassaí and Barra do Itariri. Inhabits ombrophilous forest and restinga dry forest, where a Micrurus ibiboboca predated a specimen on 06/03/2013. Marciano Junior et al. (2010) reported a bluish coloration in offsprings. This observation is confirmed from a young museum specimen (SVL ≤ 185 mm) with remnants of juvenile bluish coloration transitioning into brownish coloration.
Typhlopid, boids and colubrids from the northern coast of Bahia: A Amerotyphlops brongersmianus B Boa constrictor constrictor C Corallus hortulanus D Epicrates assisi E Eunectes murinus F Chironius bicarinatus G Chironius carinatus H Chironius exoletus I Chironius flavolineatus J Drymarchon corais K Drymoluber dichrous (juvenile) L Leptophis ahaetulla liocercus M Mastigodryas bifossatus N Oxybelis aeneus O Pantherophis guttatus P Pseustes sulphureus sulphureus Q Spilotes pullatus pullatus R Tantilla melanocephala. (Photo F by M. A. Passos; D by W. Pessoa; J, K by M. L. O. Travassos).
Boa constrictor constrictor Linnaeus, 1758
Fig.
A common species, large sized (min SVL = 430 mm, max SVL = 1850 mm). Recorded at Busca Vida, Camaçari, Imbassaí, Baixio and Costa Azul. Observed from January to November, active from 06:26 h to 21:15 h. We detected adults on ground (n = 8), leaf litter (n = 4), juveniles (SVL ≤ 640 mm) coiled on the base of bromeliad leaves (n = 2) and one specimens each on a fallen trunk, suspended branch, herbaceous vegetation, bushes and anthropogenic material. Inhabits open and forested habitats (
Corallus hortulanus (Linnaeus, 1758)
Fig.
A very rare species (see
Epicrates assisi Machado, 1945
Fig.
A single specimen was recorded in the municipality of Mata de São João in ombrophilous forest habitat with a cerrado enclave. After erected to a species level by
Eunectes murinus (Linnaeus, 1758)
Fig.
A rare species, large sized (min SVL = 1000 mm, max SVL = 3340 mm). Recorded at Praia do Forte, Imbassaí, Massarandupió and Baixio. Due to the aquatic life habit, this species was recorded only on flooded plains in the restinga (n = 3) on May and June, during periods of heavy precipitation. The earliest record was at 07:56 h when the animal was basking among reed vegetation (Juncus sp.) in a riverbed, whereas the other observations occurred around 13:00 h. Of those two, one specimen was crossing a road between two lakes and the other was basking in a flooded area among herbaceous vegetation. The species is strongly associated with wetlands, inhabiting rivers and ponds from the Atlantic forest and Amazon, but also moving on land to additionally feed and give birth (
Chironius bicarinatus (Wied, 1820)
Fig.
Chironius carinatus (Linnaeus, 1758)
Fig.
A rare species. Recorded at the Instituto da Mata in March and July. Detected in an ombrophilous remnant forest adjacent to a pasture. We observed one large specimen (total length > 1000 mm) swimming in a stream at 16:22 h, while the other record is based on a shed skin. The species inhabits forests, riparian forests, igapós, cocoa plantations, pastures and open habitats. Chironius carinatus is diurnal, semiarboreal and terrestrial (
Chironius exoletus (Linnaeus, 1758)
Fig.
A very rare species of medium size (min SVL = 190 mm, max SVL = 620 mm). Recorded at Praia do Forte, Imbassaí, Massarandupió and Costa Azul. We observed one specimen foraging on bromeliads in restinga dry forest at 08:33 h in September.
Chironius flavolineatus (Boettger, 1885)
Fig.
A common species of medium size (min SVL = 274 mm, max SVL = 1000 mm). Recorded at Busca Vida, Guarajuba, Praia do Forte, Imbassaí, Massarandupió, Baixio and Barra do Itariri. Occurs in the whole region in restinga, ombrophilous forest and urban environments. The species inhabits predominantly open habitats, but also forests, urban and disturbed environments (
Drymarchon corais corais (Boie, 1827)
Fig.
Large sized snake (min SVL = 425 mm, max SVL = 1100 mm). Recorded in the municipalities of Dias D’Ávila and Catu, where vegetation consists mainly of ombrophilous forest. It inhabits the restinga, open areas and urban environments (
Drymoluber dichrous (Peters, 1863)
Fig.
Medium sized snake (min SVL = 220 mm, max SVL = 570 mm). Recorded in the municipality of Catu in ombrophilous forest. It inhabits mainly forested habitats, transition areas and disturbed habitats (
Leptophis ahaetulla liocercus (Wied, 1824)
Fig.
A very rare species of medium size (min SVL = 595 mm, max SVL = 850 mm). Recorded at Reserva Sapiranga and Instituto da Mata. We observed a specimen on a suspended branch at 13:22 h in December. Specimens were recorded in restinga dry forests. Inhabits pastures, restinga and urban environment in other regions (
Mastigodryas bifossatus (Raddi, 1820)
Fig.
Medium sized snake (min SVL = 300 mm, max SVL = 802 mm). Recorded in the municipalities of Lauro de Freitas, Mata de São João, Catu and Jandaíra, without information on habitat. Terrestrial and diurnal, inhabits forested and deforested environments (
Oxybelis aeneus (Wagler, 1824)
Fig.
An intermediate frequent species of medium size (min SVL= 236 mm, max SVL = 754 mm). Recorded at Arembepe, Praia do Forte and Imbassaí from June to November. Found in activity between 09:05 h and 12:45 h. We observed individuals on suspended branches (n = 2) and bush (n = 1). In the region, it inhabits restinga and ombrophilous forest. In other ecoregions, it occupies also primary forests, disturbed and open habitats (
Spilotes pullatus pullatus (Linnaeus, 1758)
Fig.
A rare species of large size (in SVL = 139.1 mm, max SVL = 1600 mm). Recorded at Busca Vida, Praia do Forte and Imbassaí in July and August. We observed an individual foraging on the leaf litter at 15:46 h. It inhabits forests, open and disturbed habitats, is diurnal and semiarboreal (
Spilotes sulphureus sulphureus (Wagler, 1824)
Fig.
A very rare species. Recorded at Praia do Forte in August.
Tantilla melanocephala (Linnaeus, 1758)
Fig.
A rare species of small size (min SVL = 130 mm, max SVL = 277 mm). Recorded at Busca Vida, Praia do Forte and Imbassaí. Occurred in restinga (n = 9) and ombrophilous forest (n = 2). The recorded specimens were active at 06:00 h and 19:00 h in May and June, both foraging on soil. The species is terrestrial, fossorial, diurnal and nocturnal (
Sibynomorphus neuwiedi (Ihering, 1911)
Fig.
A rare species of small size (min SVL = 175 mm, max SVL = 455 mm). Recorded at Instituto da Mata in July and October and the municipalities of Pojuca and Catu.
Dipsadids from the northern coast of Bahia: A Sibynomorphus neuwiedi B Imantodes cenchoa cenchoa C Leptodeira annulata annulata D Taeniophallus occipitalis E Helicops angulatus F Helicops leopardinus G Philodryas nattereri H Philodryas olfersii herbeus I Philodryas patagoniensis J Clelia plumbea K Oxyrhopus petolarius digitalis L Oxyrhopus trigeminus M Phimophis guerini N Pseudoboa nigra O Siphlophis compressus P Thamnodynastes pallidus Q Erythrolamprus aesculapii venustissimus R Erythrolamprus almadensis.
Imantodes cenchoa cenchoa (Linnaeus, 1758)
Fig.
A very rare species of medium size (min SVL = 455 mm, max SVL = 670 mm). Recorded at Instituto da Mata in November (see Marques et al. 2013) and the municipality of Simões Filho. Occurs in the ombrophilous forest in the study region. The species is nocturnal and we recorded it at 20:23 h. The animal was foraging on a bromeliad. Despite its arboreal habit, I. cenchoa often forages on ground level in forests and disturbed habitats (
Leptodeira annulata annulata (Linnaeus, 1758)
Fig.
An intermediately frequent species of medium size (min SVL = 195 mm, max SVL = 325 mm). Recorded at Praia do Forte, Reserva Sapiranga, Imbassaí, Massarandupió, Baixio and Costa Azul from May to October. Occurs in wooded vegetation of restinga and ombrophilous forest. Also inhabits forests, open and dry habitats (
Taeniophallus occipitalis (Jan, 1863)
Fig.
An intermediately frequent species of small size (min SVL = 215 mm, max SVL = 325 mm). Recorded at Praia do Forte, Instituto da Mata and Reserva Sapiranga from May to November. Occurs in restinga (n = 4), disturbed ombrophilous forest (n = 1) and pasture (n = 1). Also distributed in the Amazon and Caatinga (
Helicops angulatus (Linnaeus, 1758)
Fig.
An intermediately frequent species of medium size (min SVL = 173 mm, max SVL = 810 mm). Recorded at Praia do Forte, Reserva Sapiranga, Instituto da Mata and Costa Azul in March and from September to November. Occurs in ombrophilous forest (n = 10) and restinga (n = 3). The species can be abundant in urbanized and open environments and less frequent in forest habitats (
Helicops leopardinus (Schlegel, 1837)
Fig.
A very rare species of medium size (min SVL = 109 mm, max SVL = 638 mm). Recorded at Arembepe, Imbassaí and Baixio in February and October. We found only specimens in the restinga, but vouchers originate also from forested habitats (n = 13). We observed snakes at edges of lakes and only during diurnal activity from 10:00 h to 16:12 h. However, Helicops leopardinus is known to be mainly nocturnal. It feeds on fishes and frogs (
Philodryas nattereri Steindachner, 1870
Fig.
A common species of medium size (min SVL = 295 mm, max SVL = 840 mm). Recorded at Arembepe, Guarajuba, Praia do Forte, Imbassaí, Massarandupió, Baixio, Barra do Itariri and Costa Azul during the year. We found it only in restinga (n = 38) during fieldwork, supported also by voucher specimens. It inhabits mainly open and semiarid habitats, also recorded at brejos de altitude (isolated fragments of humid forests surrounded by arid Caatinga) and disturbed habitats (
Philodryas olfersii herbeus Wied, 1825
Fig.
An intermediately frequent species of medium size (min SVL = 200 mm, max SVL = 770 mm). Recorded at Busca Vida, Arembepe, Instituto da Mata, Imbassaí, Massarandupió and Costa Azul in January and from July to December. We found it in restinga (n = 9) and disturbed areas of ombrophilous forest (n = 2). The species is diurnal and active from 07:56 h to 14:56 h. We observed snakes foraging on ground (n = 3), on leaf litter (n = 2) and in herbaceous vegetation (n = 1). The species is terrestrial and semiarboreal (
Philodryas patagoniensis (Girard, 1858)
Fig.
A common species of medium size (min SVL = 184 mm, max SVL = 848 mm). Recorded at Busca Vida, Arembepe, Praia do Forte, Imbassaí, Massarandupió, Barra do Itariri and Costa Azul from February to December. Occurs in restinga (n = 14), urbanized environment (n = 5) and ombrophilous forest (n = 3). Usually found in open and disturbed habitats (
Clelia plumbea (Wied, 1820)
Fig.
A medium sized snake (min SVL = 335 mm, max SVL = 820 mm). Recorded in the municipality of Catu. Voucher specimens were from urban habitation. Inhabits mainly forests, disturbed, and open habitats (
Oxyrhopus petolarius digitalis Reuss, 1834
Fig.
A rare species of small size (min SVL = 176 mm, max SVL = 445 mm). Recorded at Praia do Forte and Instituto da Mata in July and November. We observed animals on pasture (n = 2) near ombrophilous forest remnants. A voucher specimen was obtained from the restinga. The species is terrestrial, forages on the ground (n = 2) and is nocturnal, detected at 21:10 h. Inhabits forest and disturbed habitats (
Oxyrhopus trigeminus Duméril, Bibron & Duméril, 1854
Fig.
An intermediately frequent species of medium size (min SVL = 178 mm, max SVL = 656 mm). Recorded at Busca Vida, Arembepe, Guarajuba, Praia do Forte, Imbassaí, Massarandupió, Baixio, Barra do Itariri and Costa Azul from January to October. Occurs in restinga, ombrophilous forest and anthropic environments. The species is mainly nocturnal and we observed it from 18:05 h to 21:00 h, except for two specimens foraging at 09:50 h and 11:00 h. Oxyrhopus trigeminus is terrestrial. It was recorded on the ground (n = 5), in the leaf litter (n = 2), in bush and herbaceous vegetation (n = 1 each). It feeds on lizards, birds and small mammals. In southeastern Brazil, females are fertile from January to November (
Phimophis guerini (Duméril, Bibron & Duméril, 1854)
Fig.
A medium sized snake (min SVL = 323 mm, max SVL = 754 mm). Recorded at Guarajuba, Praia do Forte and Imbassaí (see
Pseudoboa nigra (Duméril, Bibron & Duméril, 1854)
Fig.
A medium sized snake (min SVL = 214 mm, max SVL = 870 mm). Recorded at Busca Vida and Jauá, and in the municipalities of Mata de São João and Catu. Occurs in ombrophilous forests and restinga. Pseudoboa nigra also inhabits open and disturbed habitats and forests (
Siphlophis compressus (Daudin, 1803)
Fig.
A very rare species of medium size (SVL = 738 mm). Recorded at Instituto da Mata (see Marques et al. 2013) in May. We found it in ombrophilous forest remnants foraging at ground level on the leaf litter at 21:00 h. The species inhabits forests in Amazonia and Atlantic coast (
Thamnodynastes pallidus (Linnaeus, 1758)
Fig.
A very rare species of small size (SVL = 363 mm). Recorded at the Instituto da Mata (see Marques et al. 2013). We observed it in ombrophilous forest remnants. We confirm that this snake is nocturnal, as we found one foraging on the ground at 20:30 h. The female did not contain ovarian follicles in May.
Erythrolamprus aesculapii venustissimus Wied, 1821
Fig.
A medium sized snake (SVL = 655 mm). Recorded in the municipalities of Lauro de Freitas collected in 1994, without habitat information.
Erythrolamprus almadensis (Wagler, 1824)
Fig.
Rare species of medium size (Min SVL = 136 mm, Max SVL = 450 mm). Recorded at Arembepe, Instituto da Mata, Imbassaí and Baixio in March and October. Occurs in ombrophilous forest (n = 8), restinga (n = 4), pasture and disturbed habitats (n = 1 each). Also recorded from urban environment (
Erythrolamprus miliaris merremi (Wied, 1821)
Fig.
A medium sized snake (min SVL = 145, max SVL = 642 mm). Recorded from the municipalities of Simões Filho, Dias D’Ávila and Pojuca. Occurs in ombrophilous forest remnants and disturbed areas. The species is semiaquatic with diurnal and nocturnal activities, inhabiting forests and open habitats. It feeds on fishes, caecilians, frogs, amphisbaenians, lizards, and snakes (Marques and Sazima 1994,
Dipsadids, elapids and viperids from north coast of Bahia: A Erythrolamprus miliaris merremi B Erythrolamprus poeilogyrus schotti (juvenile with a E. p. poecilogyrus-like pattern) C Erythrolamprus poecilogyrus schotti (adult) D Erythrolamprus reginae semilineatus, E Erythrolamprus taeniogaster F Erythrolamprus viridis viridis G Xenodon merremii H Xenodon rhabdocephalus rhabdocephalus I Micrurus corallinus J Micrurus ibiboboca K Bothrops erythromelas L Bothrops leucurus M Bothrops lutzi N Crotalus durissus cascavella O Lachesis muta rhombeata (Photos F, G, K by M.L.O. Travassos; O by W. Pessoa).
Erythrolamprus poecilogyrus schotti (Schlegel, 1837)
Fig.
A medium sized snake (min SVL = 150 mm, max SVL = 623 mm). Recorded from the municipalities of Camaçari, Lauro de Freitas, Mata de São João, Catu and Pojuca. It occurs in ombrophilous forest, but inhabits also cocoa plantations, pastures, swamps, and urbanized habitats (
Erythrolamprus reginae semilineatus (Linnaeus, 1758)
Fig.
A very rare species of small size (min SVL = 191 mm, max SVL = 494 mm). Recorded at the Instituto da Mata (see Marques et al. 2013) and the municipalities of Catu and Pojuca. We observed it in ombrophilous forest in February. Commonly found near ponds, forest edges, fields and disturbed habitats (
Erythrolamprus taeniogaster Jan, 1863
Fig.
A very rare species of medium size (min SVL = 147 mm, max SVL = 583 mm). Recorded at Praia do Forte, Imbassaí, and the municipalities of Lauro de Freitas, Simões Filho, Camaçari and Catu. We observed it in restinga in June, with voucher specimens also from restinga (n = 5) and ombrophilous forest (n = 4). In northeastern and southeastern Brazil, the species has a coastal distribution (
Erythrolamprus viridis viridis (Günther, 1862)
Fig.
A small sized snake (SVL = 382 mm). Recorded in the municipality of Mata de São João. Occurred in ombrophilous forest, but also in transition areas from Atlantic forests and agreste (hilly north south chain with hot and sub-humid climate) region (
Xenodon merremii (Wagler, 1824)
Fig.
A very rare species of large size (min SVL = 186 mm, max SVL = 1003 mm). Recorded at Guarajuba, Praia do Forte, Instituto da Mata, Imbassaí and Sauípe. Occurs in open areas. Voucher specimens were from deforested ombrophilous forest (n = 9) and restinga (n = 6). Terrestrial and diurnal, feeds exclusively on amphibians (
Xenodon rabdocephalus rabdocephalus (Wied, 1824)
Fig.
A medium sized snake (min SVL = 232 mm, max SVL = 654 mm). Recorded from the municipalities of Camaçari and Catu. Occurs in ombrophilous forest, cocoa plantation and pastures. The species is terrestrial and feeds on frogs and occasionally on tadpoles (
Micrurus corallinus (Merrem, 1820)
Fig.
A small sized snake (SVL= 405 mm). Recorded from the municipality of Simões Filho in ombrophilous forest.
Micrurus ibiboboca (Merrem, 1820)
Fig.
A common species of medium size (min SVL= 210 mm, max SVL = 1092 mm). Recorded at Busca Vida, Arembepe, Jacuípe, Guarajuba, Praia do Forte, Reserva Sapiranga, Instituto da Mata, Imbassaí, Sauípe, Baixio and Barra do Itariri from January to November. We observed it in restinga (n = 9), ombrophilous forest (n = 2), deforested, open and disturbed habitats (n = 3). In restinga, it inhabits the dry part of the forest. We found it active on the leaf litter (n = 9) and soil (n = 5) from 08:11 h to 17:30 h. Micrurus ibiboboca is ophiophagous (
Bothrops erythromelas Amaral, 1923
Fig.
A medium sized snake (adult SVL ca. 570 mm). Recorded from the municipalities of Camaçari and Lauro de Freitas (MZUFBA 499 and 1366, respectively). The vegetation of both municipalities varies from restinga to ombrophilous forest with enclaves of cerrado, but no precise information was available on either of the two specimens' habitats. This is a terrestrial and nocturnal species that inhabits arid and semiarid regions, from sandy and rocky areas to deciduous forests, mainly associated with the Caatinga and Cerrado (
Bothrops leucurus Wagler, 1824
Fig.
An intermediately frequent species of large size (min SVL = 115 mm, max SVL = 1600 mm). Recorded at Arembepe, Guarajuba, Itacimirim, Praia do Forte, Instituto da Mata, Imbassaí, Sauípe, Massarandupió, Baixio and Mangue Seco. We found it in restinga (n = 9), nearby human habitation and pastures (n = 1) from February to October. Bothrops leucurus is more active during nighttime (
Bothrops lutzi (Miranda-Ribeiro, 1915)
Fig.
A small sized snake (SVL = 451 mm). This species is confirmed from north of Salvador by four specimens, three by
Crotalus durissus cascavella Wagler, 1824
Fig.
A rare species of medium size (min SVL = 255 mm, max SVL = 1268 mm). Recorded at Busca Vida, Imbassaí and Massarandupió on March, August and September. Voucher specimens were from ombrophilous forest (n = 9), probably from deforested areas (
Lachesis muta rhombeata Wied-Neuwied, 1824
Fig.
A single record exists from the region based on a skin of an animal captured on a farm in the municipality of Entre Rios in 1996. The species inhabits primary forests, riparian forest, lowlands and cocoa plantations in southern Bahia. Occasionally it is found in secondary forest and surroundings. The species is nocturnal and feeds on small rodents (
The number of snake species from the northern coast of Bahia represents 38% of all species known from the state of Bahia (
Three species require taxonomic comments. First, the pitviper Bothrops lutzi from our study region, which appears isolated and far distant from the next known populations of ca. 425 km distance in Petrolina, Pernambuco, which was erroneously reported as 325 km in Lira-da-Silva (2000). We measured three specimens from Camaçari and Dias d’Ávila with ventral scale counts from 153–156, confirming
Furthermore, there are several enclaves of Cerrado type vegetation (Campo Cerrado, Campo-limpo-de-Cerrado) from Camaçari (Salvador region) 200 km north to Ribeiro do Pombal, Bahia (
Comments on the second species relate to the confusingly polymorphic species Erythrolamprus poecilogyrus divided into multiple subspecies based mainly on color pattern variation that shows also drastic changes throughout ontogeny. Offspring and juvenile pattern resembling two taxa, E. p. poecilogyrus and E. p. schotti, have been recorded by us from the study area. According to Dixon and Markezich (1992) the only key characters to distinguish E. p. poecilogyrus from E. p. schotti that do not change with ontogeny are: (1) dorsal transverse bands from head to posterior including the mid-body section in E. p. poecilogyrus versus changing to a dorsal line or interruption of transverse bands in E. p. schotti; and (2) dark to black edged cephalic shields in E. p. poecilogyrus versus relatively featureless cephalic shields in E. p. schotti. In addition, young (SVL< 350 mm) E. p. schotti from northeastern Brazil are characterized by widely spaced mid-dorsal marking.
In our study area, offspring and juvenile specimens were found displaying characters of color pattern of both taxa noted above, whereas other juveniles exhibited widely spaced dorsal markings and some specimens showed intermediate expression of dark-edging of cephalic shields. This pattern concurs with the polymorphic scenario evaluated by
A second hypothesis includes a historical component, whereby the occasional occurrence of E. p. poecilogyrus color pattern characters in the E. p. schotti range reflect a late Pleistocene/Holocene scenario of expansion and contraction of both taxa’s range, or a shifting of their contact and overlap zones, triggered by greater paleoclimatic and vegetation shifts (e.g.
As a consequence, the area around Salvador exhibits a large polymorphism in E. poecilogyrus, with specimens of each parental form, and those with prominent or only a few intermediate characters, or a combination of distinctive characters from each species, similar as was described in hybrid zones and the occurrence of relictual introgressed morphological characters in North American watersnakes (
The third species in need of discussion relates to Erythrolamprus aesculapii ssp.
When we compare the snake species richness of the northern coast of Bahia with other snake assemblages from studies with similar sampling effort and field days, the region exhibits a higher species richness (see Table
Richness of snake species: comparison between the northern coast of Bahia and other regions of Brazil.
References | Richness | Region |
---|---|---|
|
112 | Caatinga domain |
|
74 | Serra do Mar (SdM)-RJ-SP-PR-SC |
|
61 | Atlantic forest of South of state of Bahia-BA |
|
52 | Floresta Nacional de Caxiuanã-PA |
This study | 49 | North coast of Bahia |
|
47 | Parque Nacional Chapada dos Veadeiros-GO |
|
44 | Planalto do Parnaíba-CE |
|
36 | Estação Ecológica de Itirapina-SP |
|
27 | Núcleo Santa Virgínia, SdM-SP |
|
25 | Estação Ecológica Juréia Martins-SP |
|
24 | Parque Nacional dos Lençóis Maranhenses |
|
24 | Núcleo Picinguaba, SdM-SP |
|
22 | Pantanal |
|
22 | Caatinga-CE |
Stomach content in eleven species was found with lizards representing 40% of food items, amphibians 20%, mammals and snakes 15% each, fishes and invertebrates 5% each. Some of these natural history notes are complemented by references. For example, Mesquita et al. (2011) observed Philodryas nattereri to be more active during the warmest period of the day, as well as the ingestion of Ameivula ocellifera, which probably is a common prey since both species are abundant along the coastal region. In contrast, most other species recorded at mid-day were in vegetation or in water, likely due to cooler ambient temperatures. In regards to our night observations, the principal activity of Helicops angulatus at the margin of lakes and ponds related to the foraging and predation of Leptodactylus natalensis, confirming that this snake occasionally feeds on frogs (
The herpetofauna of the north coast of Bahia is mainly threatened by habitat loss and degradation, including the ongoing expansion of residential areas and hotel-resorts (
Another deleterious aspect to snake conservation is the negative human perception towards snakes. Religious beliefs and superstition transcend an ancient fear about these animals, combined with the lack of contemporary knowledge (
Twelve species were classified as common or intermediately frequent. Since snakes are difficult to sample (
1 | Rudimentary eyes; ventral and dorsal scales of equal size | Typhlopidae (Amerotyphlops brongersmianus) |
– | Developed eyes; ventral scales larger than dorsals | 2 |
2 | Presence of loreal pit; solenoglyph dentition; keeled scales | Viperidae |
– | Absence of loreal pit | 3 |
3 | Robust body; small undifferentiated cephalic scales; more than 30 dorsal scales | Boidae |
– | Distinctive cephalic scales | 4 |
4 | Proteroglyph dentition | Elapidae |
– | Aglyph or opisthoglyph dentition | Colubridae and Dipsadidae |
Viperidae
1 | Tail tip with distinguished structures | 2 |
– | Tail tip undistinguished; postocular stripe present | 3 |
2 | Tail with rattle; brown arrow shaped dorsal scales with white bordered and dark center diamond shape | Crotalus durissus cascavela |
– | Tail tip with spiked scales; orange coloration with dark diamond blotches along the body; postocular stripe present | Lachesis muta rhombeata |
3 | Dorsal scales with 19 or 21 rows; Pale brown coloration, reddish blotches half-moon shaped with circular spots on margin; fewer than 158 subcaudals | Bothrops erythromelas |
– | Dorsal scales with 21 or more rows | 4 |
4 | Dorsal coloration varies from grayish to dark brown; Dark dorsal blotches bow shaped bordered by 1–2 white scales and separated by circular blotches; venter cream and pigmented; Immaculate supralabials. 172–212 ventrals | Bothrops leucurus |
– | Ground color grayish with elongated dark blotches half-moon shaped; Occasional white spots on supralabials; 153–156 ventrals for three specimens from north of Salvador (elsewhere 161–179, |
Bothrops lutzi |
Boidae
1 | Labial pits present; dark stripes on head | 2 |
– | Labial pits absent | 3 |
2 | Deep labial pits; variable coloration, usually brown, with dark round blotches along the body; long and prehensile tail; higher than 105 subcaudals | Corallus hortulanus |
– | Shallow labial pits; amber coloration with lighter ocelli on dorsum; lateral white and brown stripes present at 1/3 of the body; lateral ocelli uniform of brownish coloration and white spots on top; 40–60 subcaudals | Epicrates assisi |
3 | Large sized snake; olive green dorsal coloration with black ocelli along the body; venter yellowish and pigmented | Eunectes murinus |
– | Grayish coloration with brown blotches; lateral brown ocelli; tail with reddish brown blotches separated by a white stripe; postocular stripe present | Boa constrictor constrictor |
Elapidae
1 | Monadal pattern with white or yellowish edges of black rings separated by red rings; black head cap from rostral to parietals; tail with black and white rings | Micrurus corallinus |
– | Triad pattern separated by red rings; black rings of similar size intercalated with white rings; 8–12 triads on body; divided cloacal plate; 212–244 ventrals; 18–30 subcaudals | Micrurus ibiboboca |
Colubridae and Dipsadidae
1 | Even dorsal scale rows | 2 |
– | Odd dorsal scale rows | 6 |
2 | Higher than 14 scale rows; apical pits presents; round pupil; black coloration and yellowish venter occasionally reaching dorso-lateral region | Spilotes pullatus pullatus |
– | Fewer than 12 scale rows; keeled paravertebral scale rows; light vertebral stripe present | 3 |
3 | Brown head; grayish-black coloration bordering the light stripe up to 1/3 of body; brown on the remaining body; 12/12/8 scale rows, rarely 12/12/10 | Chironius flavolineatus |
– | Coloration not as above | 4 |
4 | 12/12/10 scale rows; olive dorsum; light stripe bordered by black line; yellowish venter from labials; divided subcaudals with dark stripe between them | Chironius bicarinatus |
– | 12/12/8 or 14/12/8 scale rows | 5 |
5 | Olive dorsum at 1/3 of the body and brownish on the remaining portion; paravertebrals in lighter coloration; yellowish venter up to labials; dark stripe dividing dorsals and subcaudals; 132–144 ventrals | Chironius exoletus |
– | Dark olive dorsum, lighter towards the venter; white chin; yellow venter; dorsal scales on tail with yellow center; 12/12/8 or 14/12/8 scale rows | Chironius carinatus |
6 | 17 or less scale rows at midbody | 7 |
– | 19 or more scale rows at midbody | 20 |
7 | 15 scale rows on midbody | 8 |
– | 17 scale rows on midbody | 14 |
8 | 15/15/11 scale rows; keeled dorsal scales; metallic green with brown vertebral stripe; dark stripe above supralabials up to the end of head; big eye with round pupil | Leptophis ahaetulla liocercus |
– | 15/15/15 scale rows | 9 |
9 | Two black ring pattern separated by red rings; black rings separated by white or yellow rings; big and dark eyes; opisthoglyph dentition; 179–195 ventrals; 35–46 subcaudals | Erythrolamprus aesculapii venustissimus |
– | Brown or green coloration, never red | 10 |
10 | Brownish head and dorsum; eliptical pupil; dark brown bands on dorsum; 163–182 ventrals; 59–77 subcaudals; single anal plate | Sibynomorphus neuwiedi |
– | Ocelli or uniform pattern; divided anal plate | 11 |
11 | Brown head; Ocelli behind the head up to midbody; dorsum greyish to reddish-brown; yellowish venter; 160–173 ventrals; 70–77 subcaudals | Taeniophallus occipitalis |
– | Not as above | 12 |
12 | Body uniform brown; pigmented head and nucal stripe; vertebral stripe; small eye; 138–156 ventrals; 50–63 subcaudals | Tantilla melanocephala |
– | Uniform, ocelli or dark bands pattern | 13 |
13 | Dark brown or dark green coloration; juveniles present brown or redish bands separated by white or cream stripes; 157–180 ventrals; 86–110 subcaudals | Drymoluber dichrous |
– | Brown head; dorsum light brown with dark ocelli; lateral blotches of the same color; venter lightly pigmented; ≥ 165 ventrals; ≥ 87 subcaudals | Mastigodryas bifossatus |
14. | Without scale row reduction; vertebral scales modified; slender body; head strongly distinct; big eyes and elliptical pupil; brownish coloration with dark diamond shape blotches | Imantodes cenchoa cenchoa |
– | With scale row reduction | 15 |
15 | 17/17/13 scale rows | 16 |
– | 17/17/15 scale rows | 17 |
16 | Elongated head and slender body; big eyes with round pupil; brown coloration; chin and ventral gular portion yellowish or white; Dark oral mucosa | Oxybelis aeneus |
– | Smooth scales; single anal plate; 2+2/2+3 temporals; postocular brown stripe; yellow gold coloration with black and yellow spots up to midbody | Thamnodynastes pallidus |
17 | Single anal plate; juveniles present yellowish coloration with darker transversal bands; adults present approximately dark anterior up to 2/3 of the body and yellow to the remaining portion; yellow venter | Drymarchon corais corais |
– | Divided anal plate | 18 |
18 | Green-brownish coloration; single apical pit present; dorsolateral stripes from midbody to the end of tail; supralabials, chin and venter yellowish; Venter with alternating dark bands | Erythrolamprus reginae semilineatus |
– | Without apical pits | 19 |
19 | Head light-brown; supralabials cream with black border; olive dorsum; black nucal stripe followed by a cream stripe; venter yellow-cream with black blotches | Erythrolamprus miliaris merremi |
– | Dorsum black with transversal cream stripes; supralabials lighter than dorsum; white chin; reddish venter with 25–35 black bands | Erythrolamprus taeniogaster |
20 | Without apical pits | 21 |
– | With apical pits | 26 |
21 | Single internasal scale | 22 |
– | Pair of internasal scales | 23 |
22 | Dorsum light-brown or cream with dark blotches; scales strongly keeled; cream venter with black bands; 112–124 ventrals; 79–99 subcaudals | Helicops angulatus |
– | Olive coloration with dark ocelli; scales weakly keeled; red venter with black bands; white chin; 121–133 ventrals; 57–79 subcaudals | Helicops leopardinus |
23 | Brown coloration lighter on the head; white or cream supralabials, chin and venter; modified rostral scale; smooth scales | Phimophis guerini |
– | Regular rostral scale | 24 |
24 | Green coloration; juveniles present dark green with black spots along the body; supralabials, chin and anterior portion of body yellowish; 19/19/17 scale rows; >176 ventrals | Erythrolamprus viridis viridis |
– | Other color pattern | 25 |
25 | Top of the head brown with a cream or white V or Y shape mark; Dorsum present brownish bands divided by grayish stripes; dorsolateral cream stripes; orange-reddish venter with black bands; 19/19/17 scale rows | Erythrolamprus almadensis |
– | 19/19/15 scale rows; Brownish coloration, occasionally with diagonal black ribs; cream venter weakly pigmented | Erythrolamprus poecilogyrus schotti |
26 | Single apical pit | 27 |
– | Two apical pits | 30 |
27 | Body uniform green, venter in lighter coloration; long tail; divided anal plate; 164–208 ventrals; 92–132 subcaudals | Philodryas olfersii herbeus |
– | Brown pattern, never green | 28 |
28 | Brown head; coloration varies from uniform brown to grayish; White venter; divided anal plate; 166–189 ventrals; 76–113 subcaudals | Philodryas patagoniensis |
– | 19/19/17 scale rows arranged in oblique rows | 29 |
29 | Head with small blotches and stripes from internasals to postocular portion; brown coloration with bow shape blotches connected bilaterally or usually alternated | Xenodon merremii |
– | Single blotch on head bifurcated on the neck; Brown dorsum with dark bow shape blotches along the body; pigmented venter | Xenodon rhabdocephalus rhabdocephalus |
30 | Modified vertebral row; orange head; juveniles present white stripe on parietals; black nucal stripe and red-wine coloration with black bands; white venter; >230 ventrals; >105 subcaudals | Siphlophis compressus |
– | Vertebral scales not modified | 31 |
31 | Keeled scales in 19 or 21 rows; brown head; Internasals, prefrontals and labials pigmented; black postocular stripe present; dark-brown dorsum, yellowish towards the venter with black diagonal stripes | Spilotes sulphureus sulphureus |
– | Smooth scales | 32 |
32 | 19 or 21 scale rows; brown head, darker on parietals; juveniles present white stripe on parietals; brown coloration with dark blotches | Leptodeira annulata annulata |
– | Pattern black, brown or with red, black and white rings | 33 |
33 | 21 scale rows; brown head with white stripes above the eyes up to parietals; white supralabials weakly pigmented; brown-grayish coloration with dorsolateral dark stripes and white paraventral stripe; white venter with dark stripe on edge of ventrals | Philodryas nattereri |
– | 19 scale rows, single anal plate | 34 |
34 | Uniform coloration with or without irregular spots | 35 |
– | Pattern of black, red and white rings, white venter | 36 |
35 | Black or dark-brown coloration; juveniles present a white stripe on head, dark nucal stripe and red-wine coloration; 207–235 ventrals; 53–81 paired subcaudals | Clelia plumbea |
– | Black coloration with or without white blotches; juveniles present a white stripe on head, dark nucal stripe and red-wine coloration; 188–202 ventrals; 81–97 single subcaudals | Pseudoboa nigra |
36 | Black head up to parietals; supralabials grayish; red nucal stripe; triad of black and white rings separated by red rings; white chin | Oxyrhopus trigeminus |
– | Black head with red nucal stripe; juveniles present black and white coloration; adults present black and red coloration | Oxyrhopus petolarius digitalis |
We thank the curators Antônio Argôlo (UESC), Ilka Biondi (UEFS) and Rejane Lira (UFBA) and their laboratory staff for all support during visits. Magno Travassos, Mario Sacramento, Michel A. Passos, Renato Gaiga and Willianilson Pessoa for photographs. To Sara Ruane for review contributions. The Centre ECOA and Herpetofauna of the North Coast of Bahia research group for collaboration on fieldwork activities. Herpetofauna Foundation, Reptile Technologies, Lacerta Ambiental, Instituto da Mata, Floresta Sustentável Project, Busca Vida Condominium, Fazenda Natural, Fazenda Milagres, Reserva Imbassaí and the City Hall of the visited municipalities for general support. RM and EF thank CAPES for the scholarship provided.
Museums examined voucher specimens from the municipalities of the study in alphabetical order.
Amerotyphlops brongersmianus: Camaçari: MZUFBA 1725. Conde: CHECOA 2896. Mata de São João: CHECOA 1093, 1304, 1592, 2953, MZUEFS 1421. Boa constrictor constrictor: Camaçari: CHECOA 2777. Catu: CHECOA292. Mata de São João: CHECOA 2778, MZUFBA 1968. Bothrops erythromelas: Camaçari: MZUFBA 499. Lauro de Freitas: MZUFBA 1366. Bothrops leucurus: Camaçari: CHECOA 2875, MZUEFS 381, 882, 1075, MZUFBA 320, 494, 499, 501, 695, 696, 697, 698, 699, 744, 745, 749, 869, 874, 875, 878, 917, 922, 932, 937,939, 940, 996, 1220, 1223, 1225, 1226, 1228, 1239, 1241, 1242, 1249, 1257, 1281, 1901. Catu: MZUFBA 473, 476, 941, 1950, 2411, 2437. Conde: MZUFBA 1255. Dias D’Ávila: MZUEFS 1179, 1180, 1467, MZUFBA 1528, 2409. Entre Rios: MZUEFS 1745. Esplanada: CHECOA 194. Itanagra: MZUFBA 746, 876, 925, 928, 938, 1246. Jandaíra: MZUEFS 8634, MZUFBA 901. Lauro de Freitas: MZUFBA 739, 923, 930, 936, 1250, 1254, 1447, 1633, 1634, 1878, 2020, 2116, 2139, 2151, 2227. Mata de São João: CHECOA 1055, 1251, 1257, 1258, 1302, 1303, 1334, 1335, 1336, 1337, 1338, 1339, 1343, 1345, 1599, 1894, 2468, 2781, 2782, 2783, 2784, 3088, MZUEFS 488, 1021, 1107, 1425, 1426, 1427, 1429, 1507, MZUFBA 420, 495, 693, 752, 812, 931, 933, 1227, 1229, 1240, 1243, 1406, 1526, 1532, 1547, 1885, 1886. Pojuca: MZUFBA 701. Simões Filho: MZUFBA314, 487, 491, 497, 700, 747, 748, 814, 868, 909, 916, 919, 924, 1001, 1248, 1546, 1876, 1880, 1997, 2112, 2115, 2223, 2438. Bothrops lutzi: Camaçari: MZUFBA 985, 986, 1191. Chironius exoletus: Catu: CHECOA 278, 290, 291, MZUFBA 466, 467. Entre Rios:1591. Mata de São João: CHECOA 1314, 1325, 1327, 1340, MZUFBA 418, 2209. Simões Filho: MZUFBA 619. Chironius flavolineatus: Camaçari: CHECOA 2918, 2998, MZUFBA 1199. Catu: MZUFBA 610. Conde: CHECOA 1589. Dias D’Ávila: MZUEFS 1469. Entre Rios: CHECOA 1583. Itanagra: MZUFBA 401. Lauro de Freitas: MZUFBA 1277. Mata de São João: CHECOA 1297, 1298, 1326, 1328, 1575, 1896, 1897. Simões Filho: MZUFBA 1603. Clelia plumbea: Catu: CHECOA 265, 269, 294. Corallus hortulanus: Lauro de Freitas: CHECOA 2801. Crotalus durissus cascavella: Camaçari: MZUFBA 1003, 1549, 2363. Catu: CHECOA 196, MZUFBA 455. Entre Rios: CHECOA 2859. Esplanada: MZUFBA 907. Lauro de Freitas: MZUFBA 2143, 2148. Mata de São João: CHECOA 1111, 1112, 1344, 2788, 2789. Drymarchon corais corais: Catu: CHECOA 284. Dias D’Ávila: MZUEFS 1466. Drymoluber dichrous: Catu: CHECOA 176, MZUFBA 2156, 2158, 2162. Epicrates assisi: Mata de São João: CHECOA 1613. Erythrolamprus aesculapii venustissimus: Lauro de Freitas: MZUEFS 733. Erythrolamprus almadensis: Camaçari: MZUFBA 833 1284. Catu: CHECOA 276. Dias D’Ávila: MZUEFS 1463, 1464. Lauro de Freitas: MZUEFS 741, 744, MZUFBA 1283. Mata de São João: CHECOA 1418, 1419, MZUEFS: 1423, 1422. Pojuca: CHECOA 239, 240, 241, 242, 243. Erythrolamprus miliaris merremi: Dias D’Ávila: MZUEFS 1172. Pojuca: CHECOA 244. Simês Filho: CHECOA 2912. Erythrolamprus poecilogyrus schotti: Camaçari: MZUFBA 300. Catu: CHECOA 251, 268, MZUFBA 478, 765, 538. Mata de São João: CHECOA 1577, MZUFBA 410, 423, 424, 425, 426. Lauro de Freitas: MZUEFS 739. Pojuca: CHECOA 222, 223, 224, 228, 229, 230, 245, 246. Erythrolamprus reginae semilineatus: Catu: CHECOA 293, MZUFBA 487,288. Mata de São João: CHECOA 2588. Pojuca: CHECOA 234, 235, 236, 237. Erythrolamprus taeniogaster: Camaçari: MZUFBA 563. Catu: CHECOA 270, 271, 272, MZUFBA 474, 479. Lauro de Freitas: MZUFBA 1559, 2484. Mata de São João: CHECOA 1593, 2791, MZUFBA 1640. Simões Filho: MZUFBA 608. Erythrolamprus viridis viridis: Mata de São João: MZUFBA 429. Eunectes murinus: Camaçari: MZEFS 1074. Mata de São João: MZUFBA 2395. Helicops angulatus: Camaçari: CHECOA 2904, MZUFBA 333. Catu: CHECOA 255, 256, MZUFBA 461, 163, 2159. Mata de São João: CHECOA 1895, 2773. Simões Filho: MZUFBA 1935. Helicops leopardinus: Camaçari: MZUFBA 1939. Catu: CHECOA 279, 280, MZUFBA 462. Lauro de Freitas: MZUEFS 1044, MZUFBA 1286, 2140, 2152. Mata de São João: CHECOA 1247, 1260. Pojuca: CHECOA: 225, 231, 232. Imantodes cenchoa cenchoa: Mata de São João: CHECOA 2883. Simões filho: MZUFBA 2867. Leptophis ahaetulla liocercus: Catu: MZUFBA 2219. Mata de São João: CHECOA 2952. Simões Filho: MZUFBA 510. Leptodeira annulata annulata: Camaçari: MZUEFS 1090, MZUFBA 633. Catu: MZUFBA 570. Entre Rios: CHECOA 1585, MZUEFS 1744, 1746. Jandaíra: CHECOA 2965. Lauro de Freitas: MZUEFS 693, MZUFBA 493. Mata de São João: CHECOA 1089, 1255, 1330, 1331, 1332, 1341, 1590, 1601, 2779, 2780, MZUEFS 1428. Mastigodryas bifossatus: Catu: MZUFBA 841. Jandaíra:
Phimophis guerini: Camaçari: MZUFBA 1960, 2471. Mata de São João: CHECOA 1411, 1420. Philodryas nattereri: Camaçari: MZUFBA: 1961. Catu: MZUFBA 465. Mata de São João: CHECOA 1305, 1320, 1321, 1322, 1587, MZUFBA 1431, 2238, 2371. Philodryas olfersii herbeus: Camaçari: CHECOA 2421, 2906. Catu: CHECOA 257, 266. Dias D’Ávila: MZUFBA 1426. Jandaíra: 2527. Lauro de Freitas: MZUFBA 643, 2341, 2491. Mata de São João: CHECOA 1052, 1062, 1299, 1300, 1301, 3089. Philodryas patagoniensis: MZUEFS 1407. Camaçari: CHECOA 1109, 1410, 2884, 2908, MZUFBA 356, 1275, 1282, 1297, 1364, 1491, 1492, 2282. Catu: CHECOA 258, MZUFBA 1281. Lauro de Freitas: MZUFBA 1278, 1294. Mata de São João: MZUEFS 599. Pseudoboa nigra: Camaçari: CHECOA 1053, MZUFBA 492, 1323, Catu: MZUFBA 484, 485. Mata de São João: MZUFBA 421, 2435. Sibynomorphus neuwiedi: Catu: CHECOA 252, 253, 254, 259, 260, 261, 262, 263, 264, 287, 288. Mata de São João: CHECOA 2965, 3090 Pojuca: CHECOA 247. Siphlophis compressus: Mata de São João: CHECOA 2854. Spilotes pullatus pullatus: Camaçari: MZUFBA 2142. Mata de São João: CHECOA 1422, 2785, 2786, MZUEFS 1093, 1307. Simões Filho: MZUFBA 621. Taeniophallus occipitalis: Camaçari: MZUEFS 1308. Mata de São João: CHECOA 1049, 1262, 3093. Tantilla melanocephala: Camaçari: CHECOA 2065, MZUFBA 1726, 1727. Mata de São João: CHECOA 1256, 1313, 1315, 1342, 1603, 1893, 2798. Thamnodynastes pallidus: Mata de São João: CHECOA 2852. Xenodon merremii: Camaçari: CHECOA 2907, MZUFBA 396, 449, 452, 1311. Catu: CHECOA 283, MZUFBA 456, 458, 459, 460, 464, 477. Dias D’Ávila: MZUEFS 1468. Mata de São João: CHECOA 226, 1306, 2787, MZUFBA 405, 411, 850, 1007, 1437, 1527. Pojuca: MZUFBA 298. Xenodon rabdocephalus rabdocephalus: Camaçari: MZUFBA 442. Catu: MZUFBA 831, 2154.