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Booidea

Booidea is a superfamily of nonvenomous, constricting snakes within the suborder Serpentes of the order Squamata, encompassing macrostoman alethinophidian squamates known as booid snakes or boas and their relatives.^[1] It includes six families—Boidae, Calabariidae, Candoiidae, Charinidae, Erycidae, and Sanziniidae—distributed across 14 genera, 66 species, and 33 subspecies as of 2018, with origins tracing back to the Gondwanan supercontinent.^[1] Since then, additional species have been described, including a new Boa species from Brazil in 2024.^[2] The superfamily Booidea exhibits a near-circumglobal distribution, with the highest diversity in the Western Hemisphere (43 species as of 2018), followed by Eurasia (10 species), Oceania (5 species), Africa (4 species), and Madagascar (4 species).^[1] These snakes inhabit diverse environments, from tropical rainforests and deserts to temperate grasslands, and vary greatly in size, ranging from under 1 meter in length (e.g., some erycids) to over 4 meters (e.g., certain boids like Boa constrictor), with some species like the green anaconda reaching up to 8 meters.^[1] Their diets are primarily carnivorous, consisting of lizards, birds, and mammals, often captured through constriction rather than venom.^[1] Taxonomically, Booidea was established by John Edward Gray in 1825 and has undergone significant revisions based on molecular phylogenies, which have elevated several subfamilies to family status to reflect monophyletic groupings. For instance, the traditional Boidae has been narrowed to include primarily Neotropical genera, while groups like Sanziniidae (Madagascan boas) and Candoiidae (Pacific Island boas) are now recognized as distinct families. Assessments as of 2018 highlight ongoing taxonomic flux due to new phylogenetic studies, with at least 13 species elevations and one new species description between 2008 and 2018; further changes have continued since.^[1] Conservation concerns are notable, as many species face threats from habitat loss and the pet trade, prompting systematic evaluations of their status.^[1]

Taxonomy

Etymology

The superfamily name Booidea was established by British zoologist John Edward Gray in 1825, derived directly from the family name Boidae, which he introduced in the same work to group certain nonvenomous constricting snakes.^[3]^[4] The term combines the root of the type genus Boa—from Latin boa, denoting a large serpent or water snake as referenced in Pliny the Elder's Naturalis Historia—with the standard taxonomic suffixes "-idae" for families and "-oidea" for superfamilies, following conventions in early 19th-century herpetological nomenclature that extended Linnaean hierarchies to higher ranks.^[3]^[5] Members of Booidea are commonly referred to as booid snakes or true boas and their relatives, terms that emphasize their core inclusion of the Boidae family while distinguishing them from broader historical groupings like "boa-like" snakes that once encompassed pythons (now classified separately in superfamily Pythonoidea).^[6]^[4] This nomenclature reflects evolving understandings in herpetology, where Gray's initial broad familial arrangements were refined over time to reflect monophyletic lineages based on morphological and later molecular evidence.^[4]

Classification

Booidea is a superfamily of nonvenomous snakes within the suborder Serpentes and infraorder Alethinophidia of the order Squamata. Established by Gray in 1825, it encompasses a diverse group of primarily constricting snakes distributed across tropical and subtropical regions worldwide.^[7] The superfamily currently includes six recognized families, distributed among 14 genera and comprising approximately 68 species and 33 subspecies as of 2025.^[7] These families are Boidae (true boas), Erycidae (sand boas), Calabariidae (Calabar ground boa), Candoiidae (Pacific boas), Sanziniidae (Madagascan boas), and Charinidae (North American rubber boas and relatives). Recent taxonomic revisions, based on molecular phylogenetic analyses, have elevated several former subfamilies to family status, including Charinidae in 2014 and Sanziniidae following proposals in the same period. Since 2018, at least two new species have been described in Boidae: Chilabothrus ampelophis (2021) and Boa atlantica (2024).^[7]^[8]^[2] The following table summarizes the families, their key genera, and approximate species counts:

Family	Common Name	Key Genera	Approximate Species Count
Boidae	True boas	Boa, Chilabothrus, Corallus, Epicrates, Eunectes	38
Erycidae	Sand boas	Eryx, Gongylophis	15
Calabariidae	Calabar ground boa	Calabaria	1
Candoiidae	Pacific boas	Candoia	5
Sanziniidae	Madagascan boas	Acrantophis, Sanzinia	4
Charinidae	Rubber boas	Charina, Lichanura, Exiliboa, Ungaliophis	7

This classification reflects ongoing refinements in booid taxonomy, with Boidae representing the most speciose family.^[7]

Phylogenetic relationships

Booidea occupies a basal position within the Alethinophidia clade of Serpentes, forming part of the Macrostomata group alongside Pythonoidea, to which it is the sister taxon. This placement reflects the early divergence of macrostomatan snakes, characterized by adaptations for ingesting large prey, such as highly kinetic skulls. Phylogenetic analyses consistently recover Booidea as monophyletic, nested within the broader henophidian radiation that excludes blind snakes (Scolecophidia).^[9] Key support for Booidea's monophyly and internal relationships derives from multi-locus molecular datasets. Pyron et al. (2013) analyzed 12 nuclear and mitochondrial genes across 1,262 snake species, strongly supporting Booidea (including Boidae, Pythonidae, and allies) as a clade within Alethinophidia with high posterior probability. Similarly, Reynolds et al. (2014) employed 11 genes for 127 taxa covering over 80% of boid and pythonid species, confirming the group's unity and resolving intergeneric relationships, such as the paraphyly of some traditional genera like Epicrates. These studies highlight molecular congruence in placing Booidea as divergent from advanced colubroids (Caenophidia).^[9] Within Booidea, the family-level phylogeny reveals Erycidae as the basal family, with Calabariidae sister to the remaining families. Candoiidae is then sister to a clade comprising Sanziniidae, Charinidae, and Boidae. This topology aligns with both molecular and morphological data, underscoring shared synapomorphies such as reduced hindlimb rudiments manifesting as anal spurs and specialized cranial features like the elongated medial process of the prefrontal bone and posteriorly positioned maxillary process of the palatine.^[9] Earlier debates concerning the monophyly of families like Ungaliophiinae (dwarf boas) and their affinities to Neotropical or Old World boas have been largely resolved through 2020s genomic approaches. For instance, phylogenomic analyses incorporating thousands of ultraconserved elements and whole-genome data affirm the inclusion of these taxa within Boidae, eliminating prior uncertainties from limited sampling and reinforcing Booidea's overall coherence.^[10]

Characteristics

Morphology

Members of the superfamily Booidea possess a robust, cylindrical body plan adapted for constriction, featuring elongated, limbless forms with smooth to lightly keeled dorsal scales that facilitate movement across varied substrates. These snakes retain several primitive anatomical traits, including paired functional lungs—a characteristic shared with early snake lineages but lost in more derived groups—and vestigial pelvic girdles that manifest externally as small, keratinized cloacal spurs, particularly prominent in males. The body is muscular, supporting powerful coiling during prey capture, with a distinct head separated from the neck by a narrower region.^[11]^[12]^[13] The head of Booidea snakes is typically small and blunt relative to body size, equipped with specialized sensory structures for nocturnal and low-light hunting. Many species, particularly in Boidae, feature labial pits—shallow depressions in the supralabial scales housing heat-sensitive nerve endings that detect infrared radiation from warm-blooded prey. These pit organs, numbering up to 11 pairs in some boas, provide a thermal imaging capability distinct from the deeper facial pits of viperids. Eyes vary from moderately sized with vertical pupils in terrestrial forms to reduced in fossorial species, reflecting ecological adaptations.^[14]^[15] Scale patterns in Booidea are diverse but diagnostically useful for identification, with dorsal scales arranged in 25–60 rows at midbody, varying by family—such as 39–53 rows in the fossorial rubber boa (Charina bottae) or 53–69 in Boa constrictor. Ventral scales are broad and overlapping for propulsion, while the anal plate is either undivided (common in Boidae) or divided, and the tail is relatively short to moderate, terminating in a tapered point. Subcaudal scales are smooth and paired, aiding in stability.^[16]^[17] Size variation across Booidea is pronounced, ranging from small-bodied species like those in Charinidae, which attain lengths of approximately 50–85 cm, to giants in Boidae such as Boa constrictor, which can exceed 4 m in total length and weigh over 50 kg. This disparity underscores the superfamily's ecological breadth, from compact burrowers to expansive ambush predators.^[17]^[18] Sexual dimorphism is evident in most Booidea, with females generally larger and more massive than males to accommodate reproductive demands, though tail length may be relatively longer in males. Cloacal spurs, remnants of hind limbs, are well-developed in males and reduced or absent in females, serving as tactile structures during courtship.^[11]^[12] Adaptations to specific habitats are reflected in morphological specializations; fossorial members of Erycidae, such as sand boas (Eryx spp.), exhibit reduced eyes, a cylindrical body with smooth scales, and a shortened tail for burrowing efficiency. In contrast, arboreal species within Boidae, like the emerald tree boa (Corallus caninus), possess prehensile tails with enhanced grip strength, allowing secure anchorage on branches during ambush hunting.^[19]^[20]

Reproduction

Members of the superfamily Booidea exhibit diverse reproductive modes, with viviparity or ovoviviparity predominant in most families, particularly Boidae, where females give birth to live young after internal development of embryos.^[18] In contrast, the family Erycidae shows variation, with the majority of species being viviparous or ovoviviparous, but some, such as Eryx jayakari and E. muelleri, reverting to oviparity, laying eggs that hatch externally after a short incubation period of 14–66 days.^[21] The Candoiidae, represented by the genus Candoia, are ovoviviparous, retaining eggs internally until hatching occurs just before or during birth.^[22] Internal fertilization is universal across Booidea, achieved through the male's paired hemipenes, which evert during copulation to deposit sperm directly into the female's cloaca.^[23] Mating behaviors in Booidea often involve elaborate courtship rituals, including tongue flicking to assess pheromones and body wrapping to align for intromission, with males using vestigial spurs—remnants of hind limbs—to stimulate the female's cloaca.^[24] In some Boidae species, such as those in the genus Epicrates, males engage in combat rituals prior to mating, raising heads and coiling bodies in dominance displays to secure access to receptive females, a behavior ancestral to the family dating to the Paleocene.^[24] These interactions typically occur seasonally, aligned with environmental cues like rainfall or temperature increases, ensuring offspring arrive during resource-abundant periods.^[25] Gestation periods in viviparous and ovoviviparous Booidea generally last 4–8 months, varying by species and environmental conditions; for example, Boa constrictor experiences 5–8 months, while Corallus caninus (emerald tree boa) has a 6–7 month period.^[18]^[26] Clutch or litter sizes reflect body size, with larger species producing 10–60 offspring—such as up to 64 in B. constrictor—and smaller species yielding 2–10 young, often every other year due to high energetic costs.^[18] In Sanziniidae, such as Sanzinia madagascariensis, gestation can extend to 6–8 months under cooler conditions, resulting in litters of 4–16 neonates.^[27] Neonates in Booidea are precocial, emerging fully formed and independent, capable of hunting small prey immediately after birth or hatching, with no extended parental care provided.^[18] Newborns measure 30–50 cm in length and exhibit camouflage patterns distinct from adults to evade predation during early dispersal.^[18] Sexual maturity is reached at 2–5 years, depending on species and nutrition; for instance, B. constrictor matures at 2–3 years, while C. caninus females require 4–5 years.^[18]^[26] The relatively low reproductive rates in Booidea, characterized by infrequent breeding cycles and moderate litter sizes, contribute to their vulnerability in the face of habitat loss and overexploitation, as populations recover slowly from perturbations.^[28] This K-selected strategy, emphasizing larger offspring investment over quantity, underscores the need for targeted conservation measures to protect breeding sites and reduce human-induced mortality.^[28]

Distribution and habitat

Geographic distribution

The superfamily Booidea exhibits a near-circumglobal distribution, spanning tropical and subtropical regions across the Americas, Africa, Eurasia, and the western Pacific, but absent from Australia and Antarctica. This diverse range encompasses approximately 67 species across six families, reflecting adaptive radiations in varied continental and insular environments. Native distributions are primarily continental in the Old World and more fragmented in the New World, with many species showing strong regional endemism.^[7] Boidae, the most speciose family with 37 species, dominates the Neotropics, ranging from northern Mexico through Central and South America to the Lesser Antilles, including widespread species like Boa constrictor across much of this extent, the recently described Boa atlantica endemic to the Atlantic Forest of eastern Brazil, and Chilabothrus taxa endemic to Caribbean islands such as Cuba and Jamaica. Charinidae (4 species) is restricted to the Americas, from southwestern Canada southward to northwestern Colombia, with Charina bottae occurring in western North America up to elevations of 3,050 m and Lichanura trivirgata in arid southwestern regions. Sanziniidae (4 species) is entirely endemic to Madagascar and surrounding islets, exemplified by Acrantophis madagascariensis in northern forests and Sanzinia madagascariensis in eastern lowlands, reaching up to 1,600 m. Calabariidae consists of a single species, Calabaria reinhardtii, distributed across West and Central African rainforests from Guinea-Bissau to the Democratic Republic of Congo. Erycidae (13 species) spans the Palearctic and Indomalayan realms, from southeastern Europe and North Africa through the Middle East to South and Central Asia, including Eryx jaculus in Mediterranean and arid zones and Eryx conicus in the Indian subcontinent. Candoiidae (5 species) is confined to Pacific islands, from Indonesia's Sulawesi and Moluccas through New Guinea, the Solomon Islands, and Fiji to American Samoa, with Candoia aspera in the Bismarck Archipelago and Candoia bibroni extending eastward, generally below 1,525 m.^[7]^[29] Introduced populations have established beyond native ranges, notably Boa constrictor in southern Florida, where it forms breeding populations in Everglades habitats, and on islands like Puerto Rico and the U.S. Virgin Islands (St. Croix), posing ecological risks through predation on native wildlife. Some Eryx species, such as Eryx jaculus, have putative introduced or relict populations in southern Europe, including Sicily, potentially dating to ancient human-mediated dispersals. Overall elevation ranges for Booidea span sea level to approximately 3,000 m, with Andean Boidae species like certain Corallus taxa inhabiting montane forests in the tropical Andes. These distributions overlap with diverse habitats but are shaped by continental vicariance and insular isolation.^[7]^[30]

Habitat preferences

Booidea species exhibit a range of habitat preferences shaped by their diverse morphologies and physiologies, spanning terrestrial, fossorial, arboreal, semi-arboreal, and aquatic margin niches across global environments.^[31] Terrestrial and fossorial lifestyles are prominent in families like Erycidae and Charinidae. Erycidae, including genera such as Eryx, predominantly occupy arid sands and grasslands in Eurasia and North Africa, where species like the Arabian sand boa (Eryx jayakari) thrive in sandy desert substrates that facilitate burrowing.^[32] Similarly, Eryx muelleri inhabits well-vegetated arid savannahs with minimal bare soil in West Africa, preferring spots that offer cover for fossorial activity.^[33] Charinidae, encompassing Charina and Lichanura, favor temperate forests, woodlands, and grasslands in western North America, where they burrow under rocks, logs, and bark in these cooler, structured environments.^[31] Arboreal and semi-arboreal preferences dominate in many Boidae species, particularly in tropical rainforests, while Candoiidae adapt to Pacific lowland forests. Genera like Corallus in Boidae, such as Corallus annulatus, are strongly arboreal, utilizing forested canopies from sea level to 1,000 m in Central and South America for ambush hunting and shelter.^[31] These snakes often perch in dense vegetation, reflecting adaptations to humid, structurally complex rainforest niches. Candoiidae, represented by Candoia, inhabit lowland rainforests and plantations on Pacific islands below 1,525 m, exhibiting both ground-dwelling and arboreal behaviors in these insular, humid forests.^[31] Aquatic margins provide niches for certain Boidae and Sanziniidae. In Boidae, genera like Eunectes occupy riverine and swampy habitats in South America, frequently near water bodies where they exploit semi-aquatic lifestyles.^[31] Sanziniidae, including Acrantophis and Sanzinia in Madagascar, prefer humid forest leaf litter, where they remain terrestrial and utilize moist, decomposing vegetation for cover and foraging.^[31] Most Booidea species are adapted to tropical and subtropical climates, but Erycidae extend into temperate zones with behavioral adjustments like brumation to endure cooler periods. This dormancy allows them to conserve energy in seasonal environments with temperature fluctuations.^[33] Boidae show tolerance for human-modified habitats, such as agricultural edges and plantations, where species like Corallus enydris select perches in mixed farmland for hunting rodents, though they generally avoid dense urban areas.^[34] Similarly, Boa constrictor occupies semi-arid farmlands and forest remnants near human settlements.^[35] Microhabitat selection emphasizes burrowing in loose soil for fossorial species and basking sites for thermoregulation across Booidea. Erycidae and Charinidae burrow into sandy or friable substrates for refuge, while Boidae like Boa constrictor use exposed rocks or branches for basking to maintain optimal body temperatures in variable microclimates.^[32]^[31]^[35]

Behavior

Activity patterns

Members of Booidea exhibit predominantly nocturnal or crepuscular activity patterns, allowing them to avoid diurnal predators and extreme daytime heat in their often tropical or arid habitats. For instance, many Boidae, including boa constrictors (Boa constrictor), display nocturnal or crepuscular foraging, basking briefly during cooler periods to regulate temperature.^[36] In contrast, some fossorial species in Erycidae, like the javelin sand boa (Eryx jaculus), maintain strictly nocturnal rhythms synchronized to light-dark cycles, emerging at night to hunt while burrowing during the day.^[37] These circadian behaviors are entrained by environmental cues, enhancing survival in diverse ecosystems. As ectotherms, Booidea rely on behavioral thermoregulation to maintain optimal body temperatures, primarily through basking in sunlight during cooler times or seeking shade and burrows to avoid overheating. Boas select microhabitats that allow precise control, with preferred daytime temperatures around 31°C achieved via postural adjustments and shelter use.^[38] Labial pits, specialized heat-sensing organs present in many Boidae, facilitate nocturnal activity by detecting infrared radiation from warm-blooded prey, complementing their crepuscular or nighttime patterns. Temperate species, such as rubber boas (Charina bottae) in Charinidae, bask on rocks or logs to elevate body temperature before retreating to cooler refuges.^[39] Seasonal activity varies with climate; tropical Booidea remain active year-round, with peaks during wet seasons when prey availability increases. In temperate regions, Erycidae like E. jaculus enter brumation during winter, reducing metabolic rates and activity from late fall to early spring, often increasing feeding beforehand to build reserves.^[40] Brumation sites for these species may include underground burrows, providing thermal stability. Most Booidea are solitary, interacting primarily during mating seasons, though some exhibit limited social tolerance with overlapping home ranges. In Boidae, species like C. bottae occasionally form communal overwintering dens during brumation, potentially for thermoregulatory benefits.^[41] In Charinidae, species show similar conspecific tolerance in shared habitats, but without structured groups. Locomotion in Booidea is adapted to habitat, with rectilinear movement—using ventral scales and costal muscles for straight-line progression—common in heavy-bodied forms like ground-dwelling boas in Boidae for efficient travel over substrates.^[42] Sand-dwelling Erycidae, such as Kenyan sand boas (Gongylophis colubrinus), employ rectilinear crawling combined with sidewinding for propulsion through loose sand, minimizing energy expenditure.^[43] Arboreal species, including emerald tree boas (Corallus caninus) in Boidae, utilize climbing via lateral undulation and prehensile tails to navigate branches.^[44] Defensive behaviors in Booidea emphasize evasion and deterrence over aggression. In Charinidae (e.g., C. bottae), individuals coil into a ball, exposing the blunt tail as a decoy while concealing the head, and may musk or vibrate the tail to intimidate threats; feigning death is rare but occurs in stressed individuals.^[45]^[46] Other species, like B. constrictor, rely on rapid retreat or constriction if captured, aligning with their generally non-confrontational lifestyle.^[35]

Diet and feeding

Members of the superfamily Booidea are primarily carnivorous predators that rely on constriction to subdue prey, with diets dominated by endothermic vertebrates such as mammals and birds, though smaller species and juveniles often incorporate ectotherms like lizards and eggs.^[47]^[48] Larger booids, including those in Boidae, exhibit generalist feeding habits, opportunistically targeting available prey, while some arboreal forms show specialization toward avian prey.^[49] Ontogenetic shifts are common, with juveniles consuming smaller ectothermic items before transitioning to larger endotherms as gape size increases.^[47] Predatory strategies in Booidea typically involve ambush tactics, where snakes remain motionless to surprise prey, supplemented by active pursuit in arboreal or open habitats; olfactory cues are detected via the forked tongue and vomeronasal organ for tracking.^[48] Constriction coils the body around the victim, applying pressure that induces asphyxiation or circulatory arrest, facilitating digestion by immobilizing and killing the prey without venom.^[47] Prey is swallowed head-first to minimize resistance from limbs or protrusions, with maximum prey mass often reaching up to 50% of the snake's body weight in larger species.^[49] Dietary variations occur across families: Erycidae, such as species in Eryx and Charina, primarily consume rodents and geckos, with juveniles favoring lizard eggs and smaller lizards.^[50] In Boidae, genera like Boa and Eunectes target larger mammals including opossums and rodents, alongside birds.^[48]^[49] Feeding occurs infrequently, typically every 1-2 weeks, allowing time for digestion of large meals that can sustain the snake for extended periods.^[48] As apex or mesopredators, Booidea play a key role in ecosystems by controlling rodent and small mammal populations, thereby influencing community structure and reducing herbivory pressure.^[47] Their opportunistic predation helps maintain trophic balance in diverse habitats from forests to deserts.^[49]

Evolution

Fossil record

The fossil record of Booidea documents a temporal range from the Paleocene to the present day, with primitive booid snakes appearing in Paleocene deposits such as those at São José de Itaboraí in Brazil, where vertebrae indicate early members of the superfamily alongside other basal alethinophidian snakes.^[51] These early fossils, dating to around 60 million years ago, suggest that Booidea had begun to diversify shortly after the Cretaceous-Paleogene extinction event, though crown-group taxa are not confirmed until the Eocene.^[51] Definitive Eocene fossils include Messelophis variatus from the Messel Pit in Germany, a site renowned for its exceptional preservation of early-middle Eocene (approximately 47-48 million years ago) vertebrates, where articulated skeletons reveal booid characteristics such as robust vertebrae and evidence of infrared-sensing pit organs.^[52] This species, a stem boid, provides the earliest direct evidence of viviparity in snakes, with embryos preserved within the maternal specimen, indicating that live birth—a key reproductive trait in modern Booidea—evolved by the Lutetian stage of the Eocene. Another notable Eocene taxon is Eoconstrictor fischeri, also from Messel, which exhibits well-preserved labial pit organs comparable to those in extant pythons and boas, supporting the early origin of thermoreception in the superfamily.^[52] In North America, the Green River Formation (Eocene, approximately 50 million years ago) yields boid-like vertebrae and partial skeletons assigned to Boavus idelmani, a small-bodied snake with features linking it to basal Booidea, highlighting the superfamily's Laurasian distribution during the early Paleogene. Marine deposits from the same period contain fossils of Palaeophis, an extinct genus of aquatic snake with elongated vertebrae adapted for swimming, often placed near the base of Booidea or as a stem alethinophidian in European and African sites.^[53] The Miocene represents a peak in booid diversity, with numerous taxa across Eurasia and the Americas, including the extinct boine genus Bavarioboa from Oligocene-Miocene boundary deposits in Europe and western Asia, characterized by large-bodied constrictors with specialized cranial features.^[54] Overall, the fossil record underscores a gradual diversification of Booidea, with Eocene sites like Messel and Green River providing critical insights into anatomical innovations such as pit organs and viviparity that define the group today.^[52]

Biogeographic history

The superfamily Booidea originated in Gondwana, likely in South America, during the Late Cretaceous to early Paleocene, as evidenced by Paleocene fossils from Brazil, with subsequent dispersal to Laurasia in the early Eocene.^[51]^[52] Sympatric occurrence of stem boids and pythonids in Eocene Europe, including Messelophis and Eoconstrictor (stem boids) alongside Messelopython (stem pythonid), supports early intercontinental dispersal and diversification in northern regions.^[52]^[55] Molecular estimates place the divergence between Booidea and its sister group Pythonoidea in the mid-Cretaceous, around 100 million years ago.^[56] Southern lineages reflect Gondwanan vicariance, where ancestral populations were fragmented by continental drift, leading to isolated radiations in regions like South America and Madagascar. Key dispersal events shaped the group's distribution, including overland migration of Pythonidae ancestors from Laurasia to Asia via Eurasian land connections in the Paleogene.^[55] A notable trans-Atlantic dispersal, likely via rafting, explains the split between African Calabariidae and Neotropical Boidae around 40 million years ago in the Eocene, postdating the full separation of Africa and South America.^[56] Vicariance played a prominent role in other cases, such as the isolation of Madagascar from the Indian subcontinent approximately 77 million years ago, which facilitated the endemic radiation of Sanziniidae (including genera Sanzinia and Acrantophis) through allopatric speciation in the island's diverse habitats.^[56] Similarly, the Bering land bridge enabled vicariant separation within Erycidae, with the North American genus Charina diverging from Old World lineages like Eryx during Paleogene connections between Eurasia and North America. Diversification within Booidea accelerated during the Oligocene due to global cooling and aridification events that fragmented habitats and promoted adaptive radiations, particularly in tropical regions where lineages like Boidae exploited new ecological niches in forests and grasslands.^[56] Recent phylogenetic analyses, incorporating Eocene fossils like those from Geiseltal, Germany (~41-48 million years ago), provide minimum age calibrations for major splits within Booidea, such as the stem of crown Boidae, aligning with post-Cretaceous recovery and early Cenozoic tectonic shifts.^[57] These patterns underscore a combination of vicariance and long-distance dispersal in the group's evolutionary history. Contemporary biogeographic patterns highlight high endemism, such as the Candoiidae restricted to Pacific islands including Fiji, resulting from ancient vicariance across Gondwanan fragments with subsequent isolation.^[58] Recent human-mediated introductions, including species like the boa constrictor (Boa imperator) to non-native regions such as Florida, have begun to alter natural distributions, though these are anthropogenic rather than natural evolutionary processes.^[6]

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Aug 25, 2022 · They are double structures in an inverted position that are exposed during copulation. This study describes the macroscopic and histological ...
[22]
Phylogeny of Courtship and Male-Male Combat Behavior in Snakes
Sep 24, 2014 · The phylogenetic patterns of behavior reveal that male-male combat in the Late Cretaceous common ancestors of Boidae and Colubridae involved combatants raising ...
[23]
REPRODUCTIVE ECOLOGY OF BOINE SNAKES WITH EMPHASIS ...
Large body size as well as the relative larger mid-body circumference in most of the Brazilian boids may allow for increased reproductive output (clutch size, ...
[24]
Corallus caninus (Emerald Tree Boa) - Animal Diversity Web
Corallus caninus is a viviparous species with a gestation period of 6 to 7 months. Breeding does not typically begin until females are 4 to 5 years old and ...
[25]
[PDF] SANZINIA madagascariensis is one of the most
S. madagascariensis is ovoviviparous with four to sixteen young born after a gestation period of six to eight months (ross & marzec, 1990).Missing: Sanziniidae | Show results with:Sanziniidae
[26]
[PDF] REPRODUCTIVE ECOLOGY OF BOINE SNAKES WITH EMPHASIS ...
Relationship between female snout-vent length (SVL) and clutch size (left) ... This might be due to dif- ferences in habitat use and/or behavior of pregnant.
[27]
A new record for the rare and highly elusive sand boa, Eryx jaculus ...
Aug 10, 2025 · The sand boa (Eryx jaculus) is the most elusive and rare reptile species in Romania, where it occurs at its north-westernmost range limit. The ...<|control11|><|separator|>
[28]
Boas of the World (Superfamily Booidae): A Checklist With ...
Sep 1, 2018 · We provide a comprehensive checklist of all 66 species and 33 subspecies of booid snakes recognized herein, distributed among 14 genera and six families.Missing: Booidea | Show results with:Booidea
[29]
Modelling the habitat suitability of the Arabian sand boa Eryx ...
The Arabian sand boa, Eryx jayakari Boulenger, 1888, is a highly adapted species living mostly in sandy deserts of the Arabian Peninsula and southwestern Iran.
[30]
Aspects of natural history in a sand boa, Eryx muelleri (Erycidae ...
FAQs. The study found Eryx muelleri predominantly inhabits well-vegetated spots with minimal bare soil, showing significant habitat preference patterns (χ² = ...
[31]
Aspects of Habitat Selection by an Arboreal Boa (Corallus enydris ...
Jan 6, 2016 · Biologists should study the West Indian herpetofauna in a variety of situations, including those modified (subtlely to flagrantly) by human ...
[32]
Boa constrictor - Animal Diversity Web
Boa constrictor young are born fully developed and are independent within minutes of birth. Male reproductive investment is largely spent in finding mates.Missing: neonatal | Show results with:neonatal
[33]
Spatial ecology, activity patterns, and habitat use by giant pythons ...
Mar 28, 2022 · Giant pythons use rainforest, shift to open woodland seasonally, are active primarily at night, with larger snakes hunting more during the day. ...<|control11|><|separator|>
[34]
Colombian Red-Tailed Boa - Oakland Zoo
Activity and Behavior. Activity Pattern. Boa constrictors are nocturnal or crepuscular, though they bask in the sun to warm themselves in cool weather.
[35]
Rhythms in the Sand Boa, Eryx conicus - jstor
ABSTRAcr.-In the nocturnal snake Eryx conicus the light-dark cycle was a more effective syn- chronizer of diel activity than were fluctuations in ...
[36]
Thermoregulation in pythons—I. Effect of shelter, substrate type and ...
Mean preferred temperature during the day was 31·3°C. 4. 4. Values near the mean preferred temperature were maintained by basking and postural changes.
[37]
thermoregulation in the boa constrictor - jstor
The snakes were able to maintain body temperature as much as 7 C below the ground shade tempera- tures by seeking out cooler subterranean retreats. Conversely,.Missing: Boidae pythons
[38]
Food Habits of the Javelin Sand Boa Eryx jaculus (Linnaeus 1758
Oct 28, 2021 · Feeding rate increases were observed in adult females in September, perhaps to enhance body reserves before hibernation.<|control11|><|separator|>
[39]
Northern rubber boa (Charina bottae): COSEWIC assessment and ...
Feb 23, 2018 · Northern Rubber Boas overwinter in hibernacula, usually communally. In British Columbia, the snakes usually emerge from hibernation in March, ...<|control11|><|separator|>
[40]
Snake locomotion
Rectilinear locomotion is movement in a straight line. It is used mainly by large snakes such as large vipers, boas, and pythons. In rectilinear locomotion ...
[41]
https://www.canada.ca/en/environment-climate-change/services/species-risk-public-registry/cosewic-assessments-status-reports/northern-rubber-boa-2016.html
[42]
[PDF] Activity Budget and Spatial Behavior of the Emerald Tree Boa ...
Hunting and movement were both found to predominantly occur during the nocturnal. (lights off) hours, while resting was found to occur during the diurnal ( ...
[43]
Natural History of the Rubber Boa
Unlike many other snakes, they never use striking as a defense mechanism, although if handled too roughly, they will musk the holder (excrete very smelly ...
[44]
Charina bottae - Animal Diversity Web
When threatened, they curl up and stick their tail out to imitate their head, causing the predator to attack this extremely durable tail instead of their head.<|control11|><|separator|>
[45]
Gape size and evolution of diet in snakes: Feeding ecology of ...
Aug 7, 2025 · Boas of the World (Superfamily Booidea): A Checklist With Systematic, Taxonomic, and Conservation Assessments. Article. Full-text available.
[46]
[PDF] Food habits of Brazilian boid snakes: overview and new data, with ...
Most boids exploit diurnal and nocturnal preys, probably using both sit-and-wait and active tactics. They feed on the ground but boas and C. hortulanus and ...
[47]
Body size predicts prey preference but not diet breadth in pythons
Jun 6, 2023 · We hypothesise that small-bodied pythons likely include a high proportion of ectothermic prey in their diets because of gape size limitations, ...
[48]
Food Habits of the Javelin Sand Boa Eryx jaculus (Linnaeus 1758
Oct 28, 2021 · The Javelin Sand Boa, Eryx jaculus, is reported to be a predator of mammals, lizards and their eggs, and occasionally of birds and ...
[49]
[PDF] fossil snakes from the palaeocene of sao josé de itaborai, brazil. part ii.
The earliest representatives of the Boidae come from the latest Cretaceous: Maastrichtian (Rage, 1987) or perhaps Campanian (Albino, 2000). At !taboraI, the.
[50]
Exquisitely Preserved Fossil Snakes of Messel: Insight into ... - MDPI
Our knowledge of early evolution of snakes is improving, but all that we can infer about the evolution of modern clades of snakes such as boas (Booidea) is ...
[51]
Earliest record of the fossil snake Palaeophis from the Paleocene ...
Aug 7, 2025 · The earliest record of Palaeophis ever found in Denmark is here based on vertebrae described from the Paleocene/Eocene Stolleklint Clay of ...
[52]
Boine Snake Bavarioboa from the Oligocene/Miocene of Eastern ...
Aug 5, 2025 · Fossil remains of the extinct boine snake Bavarioboa, thus far known exclusively from several localities of western and central Europe, ...
[53]
The Pleistocene serpent Wonambi and the early evolution of snakes
These phylogenetic conclusions contradict the widely held 'subterranean' theory of snake origins, and instead imply that burrowing snakes (scolecophidians and ...Missing: Booidea | Show results with:Booidea
[54]
Pythons in the Eocene of Europe reveal a much older divergence of ...
Dec 16, 2020 · Still, molecular time estimates suggest that Booidea and Pythonoidea diverged in the mid-Cretaceous [11,15,19], implying a ghost lineage of at ...
[55]
[PDF] The complex evolutionary history of boid snakes - Bio-Nica.info
Since the early 1970s, boine snakes (Boidae: Boinae) have served as a prime example of a group whose current distribution was shaped.Missing: superfamily | Show results with:superfamily
[56]
new booid snake from the Eocene (Lutetian) Konservat-Lagerstätte ...
Dec 12, 2023 · We describe two exceptionally preserved fossil snakes from the Eocene Konservat-Lagerstätte of Geiseltal, located in the state of Saxony-Anhalt, Germany.
[57]
[PDF] A Taxonomic Revision of Boas (Serpentes: Boidae)
Aug 1, 2014 · The taxon comprising the current Boidae + Calabariidae now forms the superfamily Booidea (Table 1), containing the families Calabariidae ( ...