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D'Albertis python
D'Albertis python
D'Albertis python
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D'Albertis python
Scientific classification Edit this classification
Kingdom: Animalia
Phylum: Chordata
Class: Reptilia
Order: Squamata
Suborder: Serpentes
Family: Pythonidae
Genus: Leiopython
Species:
L. albertisii
Binomial name
Leiopython albertisii
(W. Peters & Doria, 1878)
Synonyms

D'Albertis' python (Leiopython albertisii), also known commonly as D'Albert's water python or the northern white-lipped python, is a species of python, a non-venomous snake in the family Pythonidae. The species is endemic to New Guinea. There are no subspecies that are recognized as being valid.[4]

Geographic range and habitat

[edit]

L. albertisii is found in most of New Guinea below 1,200 m (3,900 ft), including the islands of Salawati and Biak, Normanby, Mussau and Emirau,[5] as well as a few islands in the Torres Strait.

The type locality given is "Kapaor in Nova Guinea boreali occidentali ... et prope Andai ". The authors also stated localities for two additional specimens: "... un esemplare a Kapaor fra i Papua Onin..." and "... un secondo esemplare ad Andai presso Dorei..." (= Kapoar, Onin Peninsula and Andai, near Dorei, Irian Jaya, Indonesia).[2]

Some doubt can be cast on its occurrence on Normanby, as McDowell (1975)[6] had erroneously assigned Bara Bara to this island, rather than to the mainland of Papua New Guinea[5] in Milne Bay Province as stated by Boulenger (1898)[7] and Koopman (1982).[8]

Etymology

[edit]

The specific name, albertisii, is in honor of Italian explorer Luigi D'Albertis.[9][10]

Description

[edit]

Female adults of L. albertisii grow to an average of about 213 cm (6–7 ft) in total length (including tail). Both sexes are patternless, except for some light markings on the postoculars. The dorsum of the head is shiny black, and the upper and lower labial scales are white with black markings on the anterior edge of the scales. Body color is either brownish-violet fading to yellowish ventrally or blackish-blue fading to gray.

Behavior

[edit]

Although mostly terrestrial, L. albertisii can and is known to occasionally climb.[11] White-lipped pythons are reportedly aggressive, though this is reduced in those born and raised in captivity.[12] L. albertisii also has been observed to regularly regurgitate fur balls from its prey.[13]

Diet

[edit]

The diet of L. albertisii includes a range of small-sized to medium-sized birds and mammals.[14] Neonates and juveniles often feed on lizards. Heat sensitive pits in the upper and lower jaws are used to help locate prey during nocturnal hunting.[11]

Reproduction

[edit]

L. albertisii is oviparous. A sexually mature female may lay a clutch of about a dozen eggs. The eggs stick together in a compact pile, and the female coils around them. The hatchlings emerge after about two months of incubation and are about 38 cm (15 in) in length.[14]

References

[edit]

Further reading

[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia

D'Albertis python

View on Grokipedia
from Grokipedia
D'Albertis' python (Leiopython albertisii), also known as the northern white-lipped python, is a nonvenomous of python in the family , endemic to and several surrounding islands including Salawati, , Normanby, Mussau, and Emirau. It is distinguished by its prominent white labial scales that contrast sharply with a dark dorsal coloration ranging from brownish-violet to blackish, often fading to yellowish on the ventral surface, and features whitish postocular spots. Juveniles are uniformly dark grayish-black, developing their adult patterning as they mature. This medium-sized python can attain a snout-to-vent length of up to 2 in adults, with total lengths up to approximately 2.5 , though it possesses a relatively slender build compared to larger python . It inhabits primary and secondary lowland rainforests below 1,500 elevation, often in proximity to rivers, streams, or other sources, and exhibits a primarily terrestrial to semi-arboreal , being highly active and nocturnal. The is oviparous, with females laying clutches of 17–21 eggs seasonally between December and March, and its diet consists mainly of small mammals, supplemented by such as skinks in juveniles. Distributed across the northern and western regions of in the Indonesian provinces of Papua and West Papua, as well as , it occupies a broad range that includes the Vogelkop Peninsula, , and the Huon Peninsula. Taxonomically, L. albertisii belongs to a of New Guinean pythons that underwent revision in , incorporating former such as L. biakensis and L. huonensis as synonyms within its northern . Although classified as Least Concern on the due to its wide distribution and presumed large population, the species faces potential threats from international pet trade, with hundreds harvested annually from Indonesian since the , often exceeding export quotas and involving unmonitored domestic markets.

Taxonomy and nomenclature

Scientific classification

The D'Albertis python is scientifically classified as Leiopython albertisii (Peters & Doria, 1878), originally described as Liasis albertisii in the journal Annali del Museo Civico di Storia Naturale di Genova. This species belongs to the family within the order , representing a lineage of non-venomous constricting snakes native to the Indo-Australian region.
Taxonomic RankName
KingdomAnimalia
Chordata
ClassReptilia
Order
SuborderSerpentes
Leiopython
albertisii
The species has undergone several nomenclatural changes, with historical synonyms including Liasis albertisii Peters & Doria, 1878; Leiopython gracilis Hubrecht, 1879; albertisii Underwood & Stimson, 1990; and Bothrochilus albertisii Cogger, Cameron & Cogger, 1983. More recent synonyms, such as Leiopython biakensis Schleip, 2008 and Leiopython huonensis Schleip, 2008, were synonymized under L. albertisii based on phylogenomic analyses confirming genetic and morphological continuity. The genus Leiopython Hubrecht, 1879, encompasses white-lipped pythons and currently includes L. albertisii and L. fredparkeri Schleip, 2008 as valid species. No subspecies of L. albertisii are recognized as of 2025. The specific epithet honors the Italian explorer Luigi Maria d'Albertis, who collected specimens from .

Etymology and discovery history

The specific name albertisii honors the Italian explorer and naturalist Luigi Maria d'Albertis (1841–1901), who collected the first known specimens of this python during his expeditions in from 1872 to 1876. These expeditions, aboard vessels like the Stella and Larthaus, focused on the island's diverse and , yielding numerous novel that advanced European understanding of the region's biodiversity. The genus name Leiopython, established by Hubrecht in 1879, combines the Greek words leios (meaning "smooth") and python, alluding to the species' characteristically smooth dorsal scales, which distinguish it from more keeled relatives in the family. The initial specimens were gathered in the Arfak Mountains region of : one in April 1872 near Kapaur (Onin Peninsula) by d'Albertis himself, and another in June 1875 near Andai () by fellow explorer Odoardo Beccari. These collections formed the basis for the formal scientific description of the as Liasis albertisii in 1878 by German herpetologist Wilhelm Peters and Italian zoologist Giacomo Doria, published in the Annali del Museo Civico di Storia Naturale di Genova. This description highlighted key morphological traits, such as the black head, yellowish-brown body, and white labial scales, marking it as a significant addition to known python diversity from the Austro-Malayan subregion. Subsequent taxonomic revisions reflected evolving phylogenetic insights into python relationships. Initially classified within the genus Liasis by Peters and Doria (1878), it was transferred to Morelia in 1990 by Underwood & Stimson amid broader reclassifications of Australasian pythons based on cranial and hemipenial morphology. In 2014, molecular analyses by Reynolds et al. prompted a shift to Bothrochilus, emphasizing closer affinities with the ringed python (Bothrochilus boa). However, by 2020, phylogenomic studies reinstated Leiopython as the valid , recognizing distinct clades within the white-lipped python complex. D'Albertis's python played a pivotal role in early herpetological exploration of , as his specimens—alongside those from Beccari and others—helped illuminate the island's endemic reptile diversity during a period of intense colonial-era collecting. These efforts not only documented novel taxa but also spurred debates on python systematics, influencing decades of research into the Pythonidae's evolutionary history in the Indo-Australian .

Physical characteristics

Morphology and size

The D'Albertis python exhibits a relatively slender build compared to larger python , featuring a relatively elongate head and that is distinctly triangular and set off from the narrower neck. This body structure supports its semi-arboreal and terrestrial lifestyle in New Guinean forests. Adults are medium-sized for pythons, with females typically reaching lengths of 180–213 cm (6–7 ft) and males being smaller at 120–150 cm, though maximum total lengths can approach 2.5 m and weights around 3.5 kg. Although females tend to grow slightly larger, studies indicate no significant in body size. The species possesses heat-sensitive labial pits for detection of prey, including 2–3 diagonal pits on the rostral scale, slit-like pits on the nasals, and pits on the first and second (sometimes third) supralabials, totaling 4–6 on the upper lip across both sides. These sensory organs are integral to nocturnal hunting. follows the typical python pattern, with enlarged anterior maxillary teeth used for grasping prey, followed by smaller teeth along the jaws. Scalation includes smooth dorsal scales arranged in 43–51 midbody rows, 262–283 ventral scales, 65–79 paired subcaudal scales, and a single anal plate. These features contribute to the snake's streamlined form and ventral locomotion.

Coloration and scalation

The head of the D'Albertis python is glossy black dorsally, exhibiting a pronounced , while the supra- and infralabial scales are white with 4–6 black vertical bars or markings on their anterior edges. The body is generally patternless, with dorsal coloration varying from olive-brown or purplish-violet to nearly black in darker individuals, fading laterally to yellowish tones and ventrally to white or grayish hues; this uniform appearance is enhanced by the smooth, highly polished dorsal scales that contribute to the species' iridescent sheen. Juveniles exhibit a markedly different coloration, appearing uniformly dark grayish-black across the dorsum, venter, and subcaudals, without the whitish postocular spots that develop later in life; as they mature over 1–2 years, the dorsal color shifts to brownish-violet, with ventral and subcaudal scales becoming and yellowish tones emerging ventrolaterally. The scalation is characteristic of the , featuring smooth dorsal scales arranged in 43–51 rows at midbody, 12–13 (rarely fewer) supralabials of which the 5th–7th enter the , 16–17 infralabials, 262–283 ventral scales, an entire anal scale, and 65–79 mostly paired subcaudal scales; two pairs of parietals are present, often separated by small interparietals. Geographic variation in coloration occurs across the range, with populations from Indonesian regions such as the Sorong Peninsula and Biak Island displaying lighter, more yellowish dorsal hues compared to the darker brownish-violet tones prevalent in New Guinean specimens from areas like Fak Fak and . Scale counts also show clinal trends, with higher ventral numbers (e.g., 274–283) in western populations like those on Salawati Island versus lower counts (e.g., 262–273) in eastern ones. The dark body coloration serves a function, allowing the snake to blend effectively with the leaf litter and shaded of its .

Distribution and habitat

Geographic range

The D'Albertis python (Leiopython albertisii) is endemic to the region, with its distribution spanning Indonesian New Guinea in West Papua (including the Arfak Mountains and Onin Peninsula), and (encompassing the and ). The species occupies lowland and coastal areas across the mainland and satellite islands, reflecting its adaptation to the diverse island of the region. Island occurrences include Salawati, , , , and Batanta in ; Normanby, Mussau, Emirau, and Fergusson in . The elevation range is primarily below 1,200 m (3,900 ft), though records exist up to 1,400 m in some areas. No major historical range contractions have been documented, but the validity of records from Normanby Island remains questionable due to potential misidentifications or locality errors. Recent confirmed sightings, including on Salawati Island in the 2020s, affirm the species' persistence in parts of its core range.

Habitat preferences

The D'Albertis python primarily inhabits tropical s and monsoon forests at low to mid-elevations, typically below 800–1,200 m above . These environments include both primary and secondary regrowth, with the species showing a preference for humid, warm conditions characterized by annual rainfall exceeding 2,500 mm. It avoids arid regions and higher altitudes, confining its distribution to lowland and lower montane zones where such climatic stability prevails. Within these forests, the python favors microhabitats in the dense near streams, swamps, or other permanent sources, often resting among leaf litter, roots, and debris on the during the day. Although primarily terrestrial, it occasionally climbs low branches up to 3–5 m for ambushing prey or shelter, reflecting a semi-arboreal orientation suited to the structurally complex . This association with water bodies—evident in habitats like coastal swamps and riverine areas—underpins its common name "," despite lacking full aquatic adaptations. The species is also recorded at the edges of clearings and in disturbed secondary forests, indicating some tolerance for modified landscapes proximate to intact .

Ecology and behavior

Activity patterns and locomotion

D'Albertis' python exhibits crepuscular to nocturnal activity patterns, with individuals actively primarily at and during the night while spending daylight hours resting in shaded areas, leaf litter, or under debris. This aligns with its habitat, where it has been observed hunting from the edges of streams and swamps under low-light conditions. For locomotion, the species relies on rectilinear movement for terrestrial progression, in which specialized ventral scales and costocutaneous muscles enable straight-line advancement without significant body undulation, suitable for navigating forest floors and semi-fossorial tunnels constructed by juveniles. It is predominantly terrestrial but demonstrates limited arboreal capabilities, using ventral scale to grip branches when climbing low . In its equatorial range, D'Albertis' python shows no true , though activity levels may vary seasonally with rainfall patterns; heavy can trigger increased bouts amid otherwise consistent tropical conditions. When threatened, it responds with defensive hissing and striking, though specimens in long-term often exhibit reduced aggression over time. A distinctive trait is the periodic regurgitation of indigestible fur pellets from mammalian prey, akin to avian pellet expulsion, typically occurring days after feeding to clear the digestive tract.

Defensive behaviors

The D'Albertis python employs a range of primary defensive strategies when threatened, including rapid striking with an open mouth. Additionally, it produces hissing sounds to deter attackers. To avoid detection, the D'Albertis python relies heavily on camouflage by freezing in place, allowing its mottled coloration to blend seamlessly with the surrounding foliage and leaf litter in its habitat. Its predominantly nocturnal activity patterns further minimize encounters with diurnal predators, enhancing overall survival. Physical adaptations include the release of a foul-smelling musky from the to repel threats, a common antipredator tactic among pythons, and the body tightly to the vulnerable head and neck region. In , natural predators are few due to its and , though human activities pose the greatest overall threat. In , D'Albertis pythons often exhibit initial , including defensive displays like hissing and striking, particularly as juveniles, but they typically habituate to handling over time, reducing such responses with consistent, gentle interaction.

Diet and hunting strategies

The D'Albertis python (Leiopython albertisii) exhibits an ontogenetic shift in diet, with juveniles primarily consuming such as skinks (e.g., species in the genus Emoia) and geckos, while adults target small to medium-sized mammals including like grass rats (Melomys spp.) and marsupials such as bandicoots (family ). Juveniles transition to larger prey, including birds, as they reach maturity around 2–4 years of age, reflecting their growth in body size and gape capacity. This dietary progression aligns with the species' increasing ability to subdue and ingest larger, vertebrates. As an , the D'Albertis python employs stealthy tactics, coiling in wait near rodent burrows or bird nests and striking rapidly at opportunistic prey. It detects victims in low-light conditions using heat-sensitive labial pits on its jaws, which sense infrared radiation from , facilitating nocturnal hunts. Once captured, the snake subdues its prey through , wrapping powerful coils around the victim to induce asphyxiation before swallowing it headfirst. Adults feed every 1–2 weeks, consuming large meals relative to their body size due to their ectothermic metabolism, which supports infrequent foraging. Digestion is slow and efficient, allowing the python to extract maximum nutrients from prey; post-digestion, it often regurgitates indigestible fur or hair balls. This strategy minimizes energy expenditure while maximizing survival in their rainforest habitat.

Reproduction and life cycle

Mating system

The mating system of the D'Albertis python (Leiopython albertisii) is seasonal and aligns with the rainy period in its New Guinean range, spanning to , when rising cues reproductive activity. Oviposition follows shortly after, typically between and . Courtship involves males detecting female pheromones via tongue-flicking to locate receptive partners, often in contexts of multiple males aggregating around a , as observed in related python species. Rival males may engage in ritualized combat, intertwining their bodies in dominance displays to secure access, a documented in various pythons. The system is polyandrous, with individual females mating with several males but without forming lasting pair bonds. Copulation episodes last 1–2 hours, during which the female signals receptivity by elevating her tail to facilitate cloacal contact. Females attain sexual maturity at 3–4 years of age, once reaching a snout-vent length exceeding 140 cm, while males mature at 2–3 years and approximately 106 cm snout-vent length.

Egg production and incubation

D'Albertis' pythons (Leiopython albertisii) are oviparous, with females typically laying clutches following a seasonal breeding pattern during the summer months from to . Clutch sizes range from 8 to 21 , with captive averages around 10-14 and observed wild clutches including 17 and 21 . The possess leathery white shells and measure approximately 6–8 cm in length. Females select concealed laying sites such as moist soil, leaf litter, or hollow logs, without constructing any form of nest. Following deposition, the female coils protectively around the compact to provide maternal incubation, lasting approximately 60-70 days at temperatures around 30-32°C; males play no role in this process. Incubation exhibits temperature-dependent sex determination, wherein warmer conditions tend to yield a higher proportion of females, although this has not been specifically quantified for the .

Juvenile development

Hatchlings of the D'Albertis python (Leiopython albertisii) measure 38–60 cm in total length and weigh approximately 30–50 g at , with wild specimens around 55-60 cm. They are fully independent from birth, with no provided, and must immediately seek shelter and food to survive. Juveniles grow rapidly, often reaching 1 m in length within the first year and attaining in 3–4 years. This fast growth helps mitigate early risks but does not eliminate them. In their early stages, juveniles face high predation pressure due to their small size, making survival challenging despite their relatively large neonatal dimensions and aggressive temperament compared to smaller snake species. Their initial diet focuses on small , such as skinks, transitioning to larger vertebrates like small mammals once they exceed about 50 cm in length. Juveniles display a uniform dark grayish-black coloration, lacking the whitish spots seen in adults; these patterns develop gradually with age and growth. This ontogenetic color change is physiological and pronounced, with juvenile markings fading to the adult brownish-violet dorsal hue typically within 6–12 months.

Conservation

Population status

The D'Albertis python (Leiopython albertisii) is classified as Least Concern by the International Union for Conservation of Nature (IUCN), based on an assessment conducted in 2018 by Tallowin et al., with no subsequent updates recorded as of 2025. This status reflects its broad distribution across northern and several offshore islands, where it occupies a variety of lowland habitats below 1,200 m . Population estimates for the remain data-deficient due to systematic surveys in its remote range, though it is considered widespread and relatively common in suitable forested and areas of its core New Guinean habitat. On peripheral islands such as , Salawati, and Mussau, populations are patchier and less well-documented, subject to greater isolation effects. Overall trends indicate no significant decline across the ' range, supported by analyses of harvest levels that do not appear to threaten viability. Local extirpations may occur on small islands due to habitat and isolation, though evidence remains anecdotal without comprehensive monitoring. Monitoring efforts primarily depend on opportunistic sightings reported through platforms like , which document approximately 66 verified observations as of 2025, and trade records tracking annual exports from (historically around 800 specimens, with 380 reported in 2025, mostly wild-caught). These sources provide indirect indicators of distribution and abundance but highlight the need for more structured field studies to refine population parameters.

Threats and protection

The primary threats to D'Albertis python (Leiopython albertisii) stem from habitat degradation in the lowlands of , where logging and have fragmented rainforests essential for the species' survival. These activities reduce available arboreal and semi-aquatic habitats, potentially limiting population connectivity and increasing vulnerability to localized declines. Collection for the international pet trade represents another significant risk, with wild specimens harvested primarily from Indonesian Papua for export. The species has been regulated under Appendix II since 1977 as part of the broader family listing, requiring export permits to ensure trade does not threaten wild populations. On some islands within its range, such as those in the , introduced predators may pose additional pressures to juveniles, though this impact remains understudied. Protection efforts include occurrence within designated protected areas across , such as national parks, which help safeguard habitats from further encroachment. In , the species falls under general national laws that prohibit unauthorized taking or of native reptiles, though can be challenging in remote regions. Export from both and is further controlled through implementation, with quotas monitored to prevent . Conservation actions are largely indirect, with the species benefiting from broader regional initiatives aimed at preserving New Guinea's rainforests, such as those outlined in the Papua New Guinea National . No dedicated species-specific programs exist, but ongoing efforts to curb through community-based management and sustainable practices provide ancillary support. The future outlook for D'Albertis python remains stable provided rates are moderated, as current populations show no evidence of decline. However, island subpopulations may face heightened risks from and isolation, underscoring the need for enhanced monitoring in these areas.

References

  1. https://doi.org/10.1016/j.ympev.2020.106960
  2. https://www.researchgate.net/publication/259560586_Ecological_attributes_and_trade_of_white-lipped_pythons_Genus_Leiopython_in_Indonesian_New_Guinea
  3. https://www.iucnredlist.org/species/199628/2607789
  4. https://reptile-database.reptarium.cz/Leiopython/albertisii
  5. https://reptile-database.reptarium.cz/search.php?submit=Search&genus=Leiopython
  6. https://zookeys.pensoft.net/article/2433/
  7. https://www.gbif.org/species/2465184
  8. https://www.leiopython.de/en/taxon_01.php
  9. https://www.researchgate.net/publication/235696222_Revision_of_the_Genus_Leiopython_Hubrecht_1879_Serpentes_Pythonidae_with_the_Redescription_of_Taxa_Recently_Described_by_Hoser_2000_and_the_Description_of_New_Species
  10. https://www.leiopython.de/en/taxon_06.php
  11. http://www.leiopython.de/publications/2008%2C%20Schleip%2C%20Revision%20of%20the%20genus%20Leiopython.pdf
  12. https://coldbloodcreations.com/collection_pages/wlp.html
  13. https://doi.org/10.1670/06-182R5.1
  14. https://reptichip.com/blogs/animals/northern-white-lipped-python
  15. https://www.inaturalist.org/taxa/1161324-Leiopython-albertisii
  16. https://www.ecologyasia.com/verts/snakes-png/white-lipped-pythons.htm
  17. https://wwf.panda.org/discover/knowledge_hub/where_we_work/new_guinea_forests/area_forests_new_guinea
  18. https://amphibian-pug-rzk5.squarespace.com/s/WhiteLippedPython.pdf
  19. https://legaseaaquarium.com/pages/white-lipped-python-bothrochilus-albertisii
  20. https://www.researchgate.net/publication/224973534_Natural_history_notes_Leiopython_albertisii_Behavior
  21. https://coldblooded.com/read-blog/54_care-guide-pythons-white-lipped-pythons.html
  22. https://pmc.ncbi.nlm.nih.gov/articles/PMC12015575/
  23. https://blog.projectnoah.org/post/50919877603/pythonidae-the-pythons
  24. https://www.pacificclimatechangescience.org/wp-content/uploads/2013/06/14_PACCSAP-PNG-11pp_WEB.pdf
  25. https://www.doc-developpement-durable.org/file/Elevages/Serpents/Snake%20Mating%20Systems-Behavior%20and%20Evolution.pdf
  26. https://cites.org/sites/default/files/eng/com/ac/28/Inf/E-AC28-Inf-03.pdf
  27. https://www.snakeestate.com/pythons/white-lipped-python/
  28. https://coldbloodcreations.com/breeding/white_lipped_python_breeding_diary.html
  29. https://boids.tripod.com/whitelip.html
  30. https://www.leiopython.de/en/albertisii.php
  31. https://www.publish.csiro.au/zo/fulltext/zo12017
  32. https://cites.org/eng/parties/country-profiles/id/domestic-measures?items_per_page=All&page=0
  33. https://cites.org/sites/default/files/eng/com/ac/29/E-AC29-31-01.pdf
  34. https://cites.org/eng/app/appendices.php
  35. https://www.speciesplus.net/#/taxon_concepts/10030/legal
  36. https://png-data.sprep.org/system/files/Protected%20Fauna%20of%20Papua%20New%20Guinea.pdf
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