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Pangolin

Pangolins are mammals comprising the family within the order Pholidota, distinguished as the only placental mammals with large, overlapping scales covering most of their bodies, akin to those in and claws. These toothless insectivores subsist primarily on and , which they capture using an elongate, sticky anchored to the ribcage and capable of extending far beyond the head. Native to and , the eight extant vary in size from the 30 cm to the 1.8 m , with habits ranging from arboreal to terrestrial and predominantly nocturnal lifestyles marked by solitary behavior and defensive curling into an armored ball. All pangolin species are currently assessed by the IUCN as vulnerable to , driven chiefly by intense for their scales—prized in traditional Asian despite lacking of medicinal value—and for , rendering them among the most trafficked wild mammals. Conservation efforts, including I listings since 2016, have curbed some legal trade but face challenges from persistent illegal markets and data gaps on sizes, underscoring the need for enhanced enforcement and . Their evolutionary , with no close living relatives beyond Pholidota, highlights unique adaptations like acute olfaction over vision and scale regeneration, yet underscores vulnerability to pressures absent natural predators capable of breaching their defenses.

Etymology

Origins and Linguistic Evolution

The English term "pangolin" derives from the word pengguling, an agentive formed from the peng- (indicating a performer of an ) and the root guling or giling, meaning "to roll" or "roller," reflecting the animal's defensive of into a tight ball. This etymology is corroborated across linguistic sources, emphasizing the descriptive nature of the name in its original Austronesian context, where speakers in observed the creature's rolling posture. Early of the term appeared in 1734, when it was recorded as "Panggoeling" in descriptions attributed to Javanese and other Oriental peoples, translating to "convolutorem" (Latin for "one who rolls up"), likely via colonial interactions in the region. The word entered English by , as noted in , establishing it as a direct borrowing from dialects, with possible partial influence from pangolin, which shares the same origin through parallel and routes. In English usage, the term has remained stable without significant phonetic or semantic shifts, retaining its reference to the eight species of scaly mammals in the order Pholidota, distinct from alternative descriptors like "scaly ." Linguistically, the adoption exemplifies colonial-era loanwords from indigenous languages into Indo-European ones, preserving the onomatopoeic or behavioral essence of pengguling amid broader Austronesian lexical influences in zoological nomenclature. Variants in related languages, such as pa̍t-ki-lîm (echoing rolling or scaling traits), demonstrate parallel descriptive evolutions but do not directly impact the English lineage. No suggests pre-Malay roots for the term, as its formation aligns with Proto-Malayic patterns for nouns describing behaviors.

Physical Characteristics

Morphology and Adaptations

Pangolins exhibit a distinctive characterized by a body length ranging from 30 to 100 , excluding the which adds 10 to 90 , with weights varying from 1.5 to 33 across the eight . Their surface, including the head, trunk, limbs, and , is covered in large, overlapping keratinous scales that constitute approximately 20-25% of body mass, leaving the ventral side, inner limbs, and underside of the head soft-skinned. These scales, composed of both α- and β-keratin similar to fingernails, form a flexible dermal armor unique among mammals. The head features an elongated, tubular snout adapted for probing insect nests, small eyes indicative of reliance on olfaction and audition over vision, and reduced external ears. Lacking teeth entirely, pangolins possess a narrow, edentulous skull with dense bone for structural reinforcement. Forelimbs are stout with powerful, curved claws—particularly enlarged on digits II and III—enabling efficient excavation of termite mounds and ant nests, while hindlimbs support quadrupedal locomotion with a digitigrade stance. The tail varies by species: prehensile and grasping in arboreal forms like the black-bellied pangolin (Phataginus tetradactyla), facilitating suspension and , sometimes exceeding body length and comprising up to 47 vertebrae. In terrestrial species, it aids balance during . These traits underpin key adaptations for . Scales provide mechanical protection against predators and environmental stressors, interlocking to deflect attacks and contributing to innate immunity by forming a barrier to pathogens. When threatened, pangolins curl into a near-impenetrable , tucking vulnerable undersides inward and erecting scales via underlying musculature, a effective against large carnivores. Limb modifications support myrmecophagous , with claws optimized for penetration and scale coverage extending to limbs for during .

Sensory and Locomotor Features

Pangolins possess limited visual capabilities, characterized by small eyes suited to nocturnal or crepuscular activity, which compels reliance on olfaction and audition for prey detection and environmental awareness. Their olfactory system is acutely sensitive, facilitating the location of subterranean ant and termite colonies through chemical cues. Experimental assessments confirm that captive pangolins integrate smell, hearing, and residual vision to identify and pursue food sources, with olfaction dominating in obscured conditions. Auditory processing remains underexplored genomically, though behavioral evidence underscores its role in predator evasion and foraging. Protective adaptations include muscular closures for nostrils and ear canals, shielding against insect swarms during nest raids. Locomotor adaptations emphasize digging efficiency and habitat versatility, with robust forelimbs bearing three elongated, curved claws on each manus for excavating soil and dismantling arboreal nests. Primarily quadrupedal, pangolins ambulate with a deliberate , often dragging their tails and swaying heads to scan for scents, though terrestrial species like Smutsia temminckii can briefly shift to bipedal locomotion for transport or vigilance. Arboreal taxa, such as the black-bellied pangolin ( tetradactyla), employ semi-prehensile tails and hooked digits for proficient tree climbing, enabling access to elevated galleries. All demonstrate swimming proficiency via limb paddling, aiding traversal of water barriers in fragmented habitats.

Habitat and Distribution

Geographic Range by Species

Pangolins comprise eight extant , evenly divided between and , with distributions shaped by tropical and subtropical habitats. Asian species occupy diverse forested regions from the to and island archipelagos, while African species span equatorial forests, savannas, and woodlands across western, central, eastern, and southern extents. Ranges reflect historical biogeographic barriers, including the separating Asian island populations, and are increasingly fragmented by habitat loss and poaching pressures documented since the early 2000s. The (Manis pentadactyla) inhabits southern , , , the Himalayan foothills of and , northern , and extends into northern including and , with records from elevations up to 2,500 meters. Its range has contracted due to , with populations declining by over 90% in since the based on seizure data and field surveys. The (Manis crassicaudata) is distributed across , including , , , and , favoring lowland forests and grasslands up to 2,000 meters. Densities are lowest at range peripheries in Pakistan and Bangladesh, with core populations in showing home ranges of 2-10 km² from radio-tracking studies conducted in the . The Sunda pangolin (Manis javanica) ranges widely across , from and through Indochina to , , and Indonesian islands including , , and , up to 1,700 meters elevation. Genetic studies indicate phylogeographic structure across this extent, with home ranges averaging 1.5-4 km² in translocated individuals monitored via GPS in forests during 2020-2023. The (Manis culionensis), endemic to the region, occurs on , , Busuanga, and adjacent , with sightings in 17 of 24 municipalities as of camera-trap surveys in 2020. Its restricted range, spanning under 50,000 km², limits populations to an estimated few thousand individuals based on density models from field data. In , the white-bellied pangolin ( tricuspis) occupies and Central African rainforests from eastward to southwestern and southward to , including gallery forests and swamp edges. It remains relatively widespread, with records from 20+ countries, though has reduced densities by 50-80% in surveyed African sites since 2000. The black-bellied pangolin (Phataginus tetradactyla) has a patchy distribution in West and , from to , with gaps before reappearing in , , , and republics. Arboreal habits confine it to forested zones, where encounter rates from line-transect surveys indicate low abundances, under 1 individual per 10 km². The ( gigantea), the largest species, ranges across West and from to and , inhabiting primary rainforests, gallery forests, and secondary growth. lengths exceed 1.8 meters in Ugandan specimens, with distributions mapped across 15 countries via museum records and recent sightings up to 2023. Temminck's ground pangolin ( temminckii) is found in southern and eastern , from northward through , , , , , and into East African savannas, with home ranges of 5-11 km² documented in South African tracking studies. It prefers open woodlands and avoids dense forests, with continuous occupancy in protected areas like confirmed by annual monitoring since the 1990s.

Preferred Environments and Microhabitats

Pangolins occupy diverse environments across and , ranging from tropical forests and savannas to grasslands, woodlands, and even arid or cultivated areas, with selection influenced by species-specific adaptations for foraging on and . Terrestrial species, predominant among both and Asian pangolins, favor open habitats like savannas, dry woodlands, and agricultural edges where prey is abundant and is suitable for burrowing, while arboreal species such as the black-bellied and white-bellied pangolins ( spp.) are restricted to forested regions with ample tree cover. African ground pangolins, including the giant (Smutsia gigantea) and Temminck's (Smutsia temminckii), prefer sandy soils in woodlands and savannas proximate to water bodies, enabling efficient excavation of extensive systems up to 3.5 meters deep for and . In contrast, Asian species like the (Manis crassicaudata) thrive in grasslands, secondary forests, and semi-arid zones, demonstrating tolerance for human-modified landscapes such as farmlands, provided rocky outcrops or loose soil are available for dens. The (Manis pentadactyla) utilizes a broader spectrum, including primary forests, stands, and grasslands at elevations up to 3,000 meters, with occupancy models showing higher detection in areas of medium canopy density that facilitate while offering partial concealment. Microhabitats are typically centered around prey concentrations and defensive refugia; terrestrial pangolins excavate burrows near and mounds, often lining them with for and moisture retention, or repurpose natural features like rock crevices and bases for resting sites that deter predators. Arboreal forms select hollow trees or dense foliage for diurnal roosting, adapting to vertical microhabitats in humid forests where bark-dwelling abound. stratification studies for the reveal exclusive use of rocky terrains for burrow initiation, underscoring a preference for structurally stable microhabitats that minimize excavation effort and enhance predator evasion through rapid enclosure. These selections reflect causal adaptations to local edaphic conditions, prey distribution, and predation pressures, rather than broad environmental tolerance alone.

Behavior and Ecology

Daily and Seasonal Patterns

Pangolins demonstrate predominantly nocturnal activity rhythms, with most species emerging from burrows, nests, or curled resting positions after dusk to forage for and . Chinese pangolins (Manis pentadactyla) exhibit peak activity between 22:00 and 02:00, with overall nocturnal patterns starting after 18:00 and concentrating between 22:00 and 04:00. Similarly, Indian pangolins (Manis crassicaudata) typically exit burrows between 18:00 and midnight, remaining active through the night in a secretive, solitary manner. Sunda pangolins (Manis javanica) show unimodal nocturnal peaks around 03:00–04:00, while captive observations confirm red-light illuminated nocturnal foraging without disruption to natural rhythms. Diurnal activity is rare but documented in specific contexts, such as occasional daytime movements in white-bellied pangolins (Phataginus tricuspis) during dam-pup interactions, indicating flexibility beyond strict . Cape pangolins (Manis temminckii) in displayed one instance of strictly diurnal , suggesting intraspecific variability influenced by local conditions like prey availability or predation risk. Seasonally, activity patterns adjust to environmental cues, particularly and resources. Temminck's ground pangolins shift from predominantly nocturnal in summer to increased diurnal activity in winter, likely to minimize thermoregulatory costs in cooler conditions while maintaining body precision. Breeding behaviors show species-specific ; pangolins mate primarily in summer and fall, with lasting 6–7 months, potentially aligning activity peaks with resource abundance post-monsoon. In contrast, Malayan pangolins (Manis javanica) lack strict seasonal mating, with observations across all months, reflecting equatorial stability in tropical habitats. Pangolins do not migrate seasonally, instead maintaining stable home ranges year-round, with activity intensity varying by dry-wet cycles affecting mound accessibility.

Diet and Foraging Strategies

Pangolins are obligate myrmecophages, deriving nearly their entire nutrition from (Formicidae) and (Isoptera), with dietary analyses confirming these as the predominant prey across species. Some species, such as the (Manis pentadactyla), consume over 70 species alongside a smaller number of species, with comprising the majority of intake. Supplements may include other like larvae, , and pupae, though these constitute minor fractions of the ; vegetable matter is rare and incidental. An adult pangolin can ingest up to 70 million insects annually, reflecting high metabolic demands from their keratinous scales and low-energy prey. Devoid of teeth, pangolins rely on a specialized feeding apparatus: a long, prehensile coated in viscous that extends up to 60 —often exceeding head-body length—to lap insects directly from nests. The 's rapid protrusion and retraction, aided by modifications akin to those in anteaters, enables efficient capture of elusive prey, with adapted to break down chitinous exoskeletons of and . Forelimbs equipped with robust, curved claws excavate nests, breaking into hardened mounds or soil galleries to access colonies, a process that can disturb up to several kilograms of per bout. Foraging occurs nocturnally and solitarily, with pangolins covering home ranges of 1–10 km² depending on prey density and , prioritizing colonies via olfactory detection over visual or auditory cues. Acute guides precise targeting, allowing differentiation of versus scents and tracking subterranean trails, while minimal eyesight limits reliance on sight. Terrestrial species like Temminck's pangolin (Phataginus tetradactyla) focus on ground-level digs, increasing in resource-scarce seasons to select energy-dense prey and maintain caloric . Arboreal species, such as the (Manis javanica), integrate vertical climbing and branch-tearing to raid tree-nesting colonies, adapting strategies to canopy microhabitats. Seasonal shifts occur, with drier periods prompting extended activity windows or prey specialization to offset reduced availability, underscoring limited dietary flexibility constrained by morphological specialization.

Reproduction and Development

Pangolins are solitary mammals that mate infrequently, with males locating receptive females via pheromones and approaching cautiously before mounting from the side to navigate the female's scaled armor. Mating sessions are brief, typically lasting under 40 minutes in captive observations of species like the (Manis pentadactyla). Reproductive cycles vary by species and environment; for instance, wild Chinese pangolins exhibit seasonal mating from November to March, while captive individuals and some Asian species like the (Manis javanica) show year-round breeding potential. Gestation lengths differ across species, with African tree pangolins (Phataginus tricuspis) averaging around 139 days and Asian species such as the Malayan pangolin (Manis javanica) ranging from 154 to 203 days in captivity. pangolins have a prolonged of 6 to 7 months, often resulting in births from to September following winter-spring matings. Females typically produce a single offspring per , though litter sizes of one predominate across genera, with sex ratios at birth near 1:1 in observed captives (7 females to 8 males among 15 births). Newborn pangolins, termed pangopups, weigh 170–450 grams depending on species and emerge hairless except for soft, pliable scales that harden within hours to days post-birth, providing initial protection. Maternal care is exclusively female-driven; the mother nurses the pup for approximately 3 months while carrying it clinging to her back or tail during foraging and movement. Pups begin accompanying the mother on foraging trips after and remain dependent until nearly adult size, with independence achieved around 4–5 months in some species, though exact timelines vary. Sexual maturity is reached early, often by 6–12 months of age; Sunda pangolins may breed as young as 6–7 months, while general estimates place it at one year for most species. data indicate physiological flexibility, with non-seasonal possible under controlled conditions, contrasting wild seasonal patterns and highlighting environmental influences on timing. Limited wild observations underscore gaps in natural details, primarily derived from captive studies.

Social Interactions and Natural Predators


Pangolins exhibit predominantly solitary social structures, with individuals typically interacting only during mating periods or when females care for offspring. Males and females do not form lasting pair bonds, and encounters between adults outside of reproduction are rare, often limited to agonistic interactions such as fights during mating seasons from May to July. Genetic analyses indicate a primarily polygynous mating system among Chinese pangolins, where some females show low mate fidelity. Courtship behaviors are minimal, with males adopting a ventrolateral position for copulation without elaborate displays.
Maternal care represents the primary non-reproductive social interaction, as females give birth to a single offspring after a period varying by , typically carrying the young on their or back during . protect juveniles by curling into a defensive ball around them when threatened, reducing exposure until the young can fend for themselves after several months. Juveniles remain dependent on the for and , riding on her base during activities, before dispersing independently. Natural predators of pangolins are limited due to their scales, which provide flexible armor, and primary mechanism of rolling into a tight to vulnerable undersides. Large carnivores such as lions, leopards, and spotted can occasionally prey upon them by prying open the curled form or targeting unarmored areas, particularly vulnerable juveniles. Some deploy additional deterrents, including sharp claws for slashing and release of a foul-smelling from anal glands akin to spray. Despite these adaptations, predation pressure is low compared to anthropogenic threats, as the armored posture effectively thwarts most attempts by smaller predators or opportunistic feeders.

Taxonomy and Evolution

Species Classification

Pangolins comprise the monotypic family within the mammalian order Pholidota, which includes three extant genera and eight recognized divided phylogenetically between Asian and African clades. The genus encompasses four Asian , characterized by terrestrial habits and overlapping distributions in subtropical forests and grasslands. The African genera (two arboreal adapted to tree-climbing with prehensile tails) and (two ground-dwelling with robust builds for burrowing) reflect convergent adaptations to similar myrmecophagous diets despite geographic separation. The following table enumerates the species with their scientific and common names, grouped by genus:
GenusScientific NameCommon Name
M. pentadactyla
M. crassicaudata
M. javanica
M. culionensis
P. tricuspis
P. tetradactylaBlack-bellied pangolin
S. gigantea
S. temminckiiTemminck's ground pangolin
This classification, established through morphological and genetic analyses, underscores the family's isolation from other mammals, with no close living relatives outside Pholidota; fossil evidence supports divergence from xenarthran-like ancestors around 60 million years ago, though extant taxonomy remains stable without recent revisions.

Phylogenetic Relationships

Pangolins (order Pholidota) are classified within the placental mammals (), specifically in the cohort of the superorder Laurasiatheria, where they form the mirorder as the to Carnivora. This positioning is primarily supported by molecular phylogenies derived from concatenated analyses of mitochondrial genomes and multiple nuclear loci, which consistently recover Pholidota + Carnivora as a to the exclusion of other laurasiatherians like and Cetartiodactyla. Earlier morphological hypotheses linking Pholidota to (e.g., due to shared myrmecophagous adaptations like elongated snouts and sticky tongues) have been refuted by these genetic data, attributing such traits to driven by similar insectivorous diets rather than shared ancestry. The divergence between Pholidota and Carnivora is estimated at approximately 70–80 million years ago during the , based on Bayesian relaxed-clock models calibrated with fossil constraints from laurasiatherian stem taxa. Within , pangolins represent a highly derived lineage, with genomic evidence indicating accelerated in traits related to scale formation (e.g., keratin-associated genes) and sensory adaptations, though no unique synapomorphies beyond keratinous scales unite them exclusively with carnivorans at higher levels. Among the eight extant pangolin species (four African: Smutsia gigantea, S. temminckii, Phataginus tricuspis, P. tetradactyla; four Asian: Manis crassicaudata, M. javanica, M. pentadactyla, M. culionensis), molecular phylogenies reveal paraphyly of African taxa. Ground-dwelling African species in Smutsia form the basal lineage, diverging around 38–45 million years ago (Oligocene), followed by arboreal African Phataginus (sister to Asian Manis, split ~28–38 million years ago in the Eocene–Oligocene), with Asian species monophyletic and further subdivided: M. pentadactyla (Chinese) basal among Asians (~17 million years ago), then M. crassicaudata (Indian, ~10 million years ago), and a clade of M. javanica + M. culionensis (Malayan and Philippine, ~5–7 million years ago). These relationships are robust across datasets including full mitogenomes, 13 protein-coding genes, and nine nuclear markers, though incomplete lineage sorting and low genetic diversity in some species (e.g., due to historical bottlenecks) necessitate caution in interpreting shallow nodes.

Fossil Record and Evolutionary History

The fossil record of Pholidota is sparse, with most specimens comprising isolated osteological elements rather than complete skeletons, reflecting both rarity of preservation and specialized burrowing habits that limit fossilization. The earliest definitive pholidotans date to the middle Eocene of , approximately 47–50 million years ago, exemplified by Eomanis waldi from the in , which preserves evidence of keratinous scales and anteater-like dental reductions adapted for . Subsequent Oligo-Miocene fossils, such as Necromanis species from and (around 16–33 million years ago), further document early diversification in , with traits like elongated snouts and reduced dentition indicating continuity with modern forms. African pholidotan fossils emerge later, with the earliest records from the Miocene-Pliocene boundary, including a partial skeleton from Langebaanweg, South Africa, dated to about 5 million years ago, suggesting dispersal from Eurasia via the Arabian Peninsula during periods of climatic connectivity. Pleistocene remains, such as a humerus of Smutsia olteniensis from Romania (1.9–2.2 million years ago) and trackways from South African aeolianites (90,000–140,000 years ago), represent late occurrences in both continents, but provide limited insight into genus-level transitions due to fragmentation. No pre-Eocene pholidotans are known, underscoring the order's relatively recent origin within Placentalia compared to more basal eutherians. Phylogenetically, Pholidota forms a monophyletic within , with estimates placing its divergence from (its probable sister group in the informal assemblage) at 56.8–67.1 million years ago, shortly after the Cretaceous-Paleogene boundary. This timeline aligns with a Eurasian cradle of , where early pholidotans likely adapted to forested paleoenvironments amid post-extinction ecological vacancies, evolving epidermal scales from modified follicles via co-option of genes like EDAR and FGFR2, distinct from squamation. Fossil evidence supports limited morphological stasis, with modern Manis retaining Eocene-grade features, though genomic analyses reveal in sensory and immune loci, potentially linked to solitary, insectivorous niches. Debates persist on exact interordinal affinities due to conflicting morphological (e.g., xenarthran-like ankle traits) and molecular signals, but favors a carnivoran alliance over outdated pilosean groupings.

Ecological Role

Insect Population Control

Pangolins exert significant influence on insect populations through their specialized diet, which consists almost exclusively of and . These myrmecophagous and termitophagous mammals use their elongated, sticky tongues to extract from nests, consuming up to 20,000 individuals per day during active foraging periods. Over an annual cycle, a single adult pangolin may ingest more than 70 million and , with diet composition varying by and season but dominated by a few prevalent taxa. This predation regulates and abundances in tropical and subtropical ecosystems, mitigating outbreaks that damage crops, timber, and . Pangolins preferentially target subterranean and arboreal colonies, disrupting mound-building activities and reducing biomass peaks, as observed in dietary analyses from regions like where consumption correlates with seasonal prey availability. One estimate suggests an individual pangolin's equates to safeguarding over 40 acres (16 hectares) from termite-induced degradation, underscoring their function as natural biocontrol agents in forests and savannas. Ecological studies highlight pangolins' selective foraging, which focuses on pestiferous species like certain Anoplolepis and mound-forming , thereby influencing community dynamics without broadly depleting beneficial roles. In areas with declining pangolin numbers due to pressures, densities have shown localized increases, implying a measurable suppressive effect under normal population levels. However, quantitative field experiments remain limited, with most evidence derived from and observational data rather than controlled exclusion trials.

Interactions with Other Species

Pangolins primarily interact with other species through predation dynamics, where they serve as prey for various carnivores and reptiles. African species face threats from leopards (Panthera pardus), spotted hyenas (Crocuta crocuta), and lions (Panthera leo), which attempt to access the curled pangolin despite its armored defense. These predators often abandon attacks due to the scales' toughness and the pangolin's ability to emit a foul-smelling from anal glands, deterring further engagement. Pythons and other large snakes may also prey on juveniles or smaller individuals, exploiting vulnerabilities during foraging. Beyond predation, pangolins exhibit commensal relationships via their burrowing behavior, which benefits co-occurring s without reciprocal advantage to the pangolin. In Asian habitats, Chinese pangolins (Manis pentadactyla) create burrows that multiple species co-utilize, fostering spatially convergent interactions and altering local vertebrate assemblages toward greater diversity. These structures act as refugia in disturbed environments, such as post-fire forests, accelerating multi-species coexistence and by providing shelter and potentially aiding soil aeration for . Interspecific competition occurs with other myrmecophagous mammals sharing and resources, influencing distribution patterns. African ground pangolins (Smutsia temminckii) overlap with aardvarks ( afer), leading to resource partitioning or exclusion in high-density zones. Such trophic overlaps can limit pangolin efficiency, particularly in fragmented habitats where prey colonies are depleted by multiple consumers. No evidence supports mutualistic with prey insects, as pangolins function as strict predators in these chains. ![Pangolin defending itself from lions (Gir Forest, Gujarat, India)](./assets/Pangolin_defending_itself_from_lions_Gir_Forest%252C_Gujarat%252C_India

Human Interactions

Historical and Cultural Significance

The term "pangolin" derives from the word pengguling, meaning "the one who rolls up," reflecting the animal's defensive behavior of into a . This was adopted in European descriptions following encounters in , highlighting early observations of their unique morphology by traders and explorers. Historically, pangolin scales have been utilized in the fabrication of protective armor, with a notable example being a seventeenth-century presented to the Prince of Wales (later King George IV) in 1820 by the . Such applications underscore the perceived durability of their keratinous scales, akin to overlapping plates, which inspired human adaptations for defense in regions where pangolins were accessible. In various cultures, pangolins hold symbolic value as emblems of and ; for instance, among certain communities, they are invoked in rituals to aid infertile individuals, symbolizing the overcoming of reproductive challenges due to the animal's reproductive success despite its solitary nature. In Zimbabwean traditions, pangolins are regarded as harbingers of good fortune, with beliefs prohibiting their harm to avoid misfortune, a rooted in their rarity and enigmatic appearance. Additionally, Temminck's ground pangolins (Smutsia temminckii) have been employed in sacrificial practices to forecast rainfall patterns, leveraging their burrowing habits as indicators of environmental cues. In , pangolins feature in legends depicting them as subterranean wanderers capable of global travel underground, a that parallels their modern exploitation through international trafficking networks. Across cultures, their armored form has positioned them as motifs of , though these attributions stem from observational anecdotes rather than empirical validation of mystical properties.

Traditional Medicine and Nutritional Uses

In (TCM), pangolin scales, known as Squama Manitis, have been used for centuries to purportedly promote in women, reduce swelling, activate blood circulation, and treat conditions such as and blockages. Practitioners prescribe scales to clear bodily "blockages" and relieve wind-dampness, often in powdered form or soaked in . However, scientific reviews find no reliable evidence supporting these claimed medicinal values, attributing any perceived effects to or unrelated factors rather than inherent properties of the keratin-based scales. In 2025, excluded pangolin-derived formulae from its , reflecting acknowledgment of the lack of proven therapeutic efficacy amid pressures. Across , traditional healers utilize up to 22 pangolin body parts to address ailments categorized under 17 international classifications, with scales and bones most frequently prescribed for , convulsions, and spiritual protection. In , 13 parts are employed for various conditions, including financial rituals and of convulsions, based on knowledge passed through generations. similarly employs scales for circulation stimulation and , with practitioners viewing pangolins as substitutable by other species despite persistent demand. These uses stem from cultural beliefs in the animal's mystical or curative properties, though empirical validation remains absent, and overharvesting has intensified scrutiny. Pangolin serves as a nutritional and cultural resource, consumed as a protein source in rural and as a in parts of , where it is valued for purported kidney benefits in and . African species rank highly in surveys, scoring nearly nine out of ten among available wild , driving local trade over scale exports in some regions. Some consumers attribute supplementary to the , integrating it into diets for enhancement, though specific compositional data confirming superior benefits over common proteins is unavailable. Historical records indicate longstanding consumption across range countries for sustenance and status, predating modern trade dynamics. All eight pangolin species have been listed under Appendix I of the Convention on International Trade in Endangered Species () since October 2017, prohibiting international commercial in wild specimens and requiring non-detriment findings for any of captive-bred individuals, which remain negligible due to unsuccessful large-scale breeding efforts. Many range states, including and , have enacted domestic bans on pangolin and possession, though enforcement varies and some stockpiled scales from pre-ban seizures are permitted for limited domestic use in under quotas, such as China's 2024 allocation of scales equivalent to pangolins poached decades ago. Legal trade volumes are thus minimal, often confined to scientific or pre-Convention specimens, with no evidence of sustainable captive production meeting demand. Illegal dominates pangolin , driven primarily by Asian demand for scales in purported medicinal remedies and as a , with African populations increasingly targeted as Asian stocks deplete. Global seizures from 2015 to 2024 totaled over 370 metric tons of scales, conservatively estimated to derive from 655,000 to 1.1 million pangolins, though actual likely exceeds this due to undetected shipments. networks span —key suppliers like and —to Asian consumers, utilizing maritime containers disguised as legal goods, with post-2020 pandemic disruptions causing a temporary slump that has partially persisted but not eradicated flows. In , court-documented cases peaked in 2018 before declining amid stricter border controls, yet persistent domestic markets and online sales indicate ongoing circumvention of bans. Enforcement dynamics reveal systemic challenges: low prosecution rates in source countries, corruption in transit hubs, and weak demand-side penalties sustain profitability, with scales fetching up to $500 per kilogram despite bans. While seizures highlight operational successes—such as multi-ton hauls in 2023—underreporting and data gaps in CITES trade records hinder precise volume assessments, underscoring that legal prohibitions have curbed but not halted the trade's scale relative to pre-2017 levels. Population impacts from this illicit harvest remain acute, as pangolins' low reproductive rates preclude recovery from annual losses in the hundreds of thousands.

Threats

Habitat Loss and Fragmentation

Habitat loss for pangolins arises primarily from associated with , commercial , operations, and infrastructure development across their ranges in and Asia. In , palm oil production has driven extensive forest conversion, contributing to some of the world's highest rates, with suitable pangolin habitats diminishing rapidly due to these activities. In , habitat degradation stems from agricultural encroachment, , and infrastructural projects, such as those in Uganda's area, which directly erode forested and environments critical for pangolin foraging and burrowing. Fragmentation exacerbates these losses by dividing contiguous habitats into isolated patches, hindering dispersal for these solitary mammals that require large home ranges—often spanning several square kilometers—for locating and colonies. This isolation reduces , elevates risks, and heightens vulnerability to events in small remnant populations, as observed in modeling of white-bellied and extirpations linked to habitat reduction over the past two decades. For the , fragmentation combined with low population densities further threatens persistence by limiting movement and increasing exposure to human disturbances. Pangolins' sensitivity to such changes compounds pressures, as fragmented edges bring individuals into closer proximity with human settlements and roads, facilitating incidental encounters and harvest. Empirical studies indicate that habitat alterations, including , have driven occupancy declines; for instance, higher human development indices correlate with reduced presence in potential habitats. In , widespread fragmentation from urban and agricultural development has contributed to local extinctions alongside . While precise quantification of habitat loss attributable solely to fragmentation remains challenging due to overlapping threats, the U.S. Fish and Wildlife Service notes pangolins' particular intolerance to human-induced disturbances, positioning habitat integrity as a core factor in their vulnerability across all eight . models underscore that without addressing these dynamics, even protected areas may fail to sustain viable populations amid ongoing land-use pressures.

Poaching Pressures and Population Impacts

Poaching targets pangolins primarily for their keratin scales, used in traditional Chinese medicine for purported remedies against ailments like arthritis and cancer despite lacking scientific evidence, and for their meat, valued as a delicacy in parts of Asia including China and Vietnam. Demand from these markets drives the illegal trade, with African species increasingly exploited as Asian populations dwindle. Annual poaching estimates for African pangolins range from 400,000 to 2.7 million individuals, though actual figures likely exceed seizure data, which represent only a fraction of the trade. Seizures of pangolin scales and products underscore the scale of poaching pressures; between 2016 and 2024, global incidents involved an estimated half a million pangolins across 75 countries and 178 trade routes. Notable examples include over 9.4 tonnes of stockpiled scales seized in in 2024, the largest such confiscation globally since January 2020, and a post-2018 peak decline in seizures reflecting partial enforcement gains but persistent . In , approximately 98% of poached pangolins are initially harvested for meat, with scales often a secondary product, highlighting regional patterns exacerbating dynamics. Population impacts from are severe, with all eight classified by the IUCN as threatened and undergoing ongoing declines, three as . Over the past decade, more than one million pangolins have been trafficked, contributing to documented reductions such as an 80% drop in the over 21 years and 50% declines in white-bellied and giant ground pangolins. In , has led to local extinctions across most habitats, shifting pressure to sources. These losses compound genetic bottlenecks and reduced reproductive viability, as pangolins' solitary, nocturnal habits hinder accurate censuses and recovery monitoring. Despite bans since 2017, persists, with one pangolin estimated poached every three minutes as of 2019 data, underscoring enforcement gaps in source countries.

Natural vs. Anthropogenic Risks

Pangolins face predation from large carnivores such as lions, leopards, , and pythons, which target them despite their keratin scales and defensive curling behavior. These natural predators exploit pangolins primarily during vulnerable periods, like when juveniles are less armored or adults are foraging nocturnally, but successful attacks remain infrequent due to the animal's armor, which resists penetration by most claws and teeth. Limited empirical data on wild mortality rates indicate that predation contributes to baseline population turnover, yet historical coexistence suggests it does not drive net declines in undisturbed habitats. Other natural risks include parasites, such as ticks on scales, and sporadic infections, though documented cases in free-ranging pangolins are rare and often tied to environmental stressors rather than epizootics. In wild Taiwanese pangolins, accounts for a significant portion of observed morbidity, potentially from intraspecific conflicts, falls, or predator encounters, but precise attribution to purely natural causes versus incidental influences remains challenging without necropsy data. Anthropogenic risks, conversely, impose outsized pressures through direct for scales and meat, which has fueled collapses across Asian and species, with volumes exceeding millions of individuals annually in peak years like 2010-2015. from and reduces grounds, exacerbating vulnerability to both predators and hunters, while incidental deaths from electric fences and roads compound losses—e.g., shocking levels of electrocutions reported in southern ground pangolins. Genomic and demographic analyses confirm recent anthropogenic-driven bottlenecks, with effective sizes plummeting post-1950 due to rather than climatic or predatory shifts. Empirical evidence underscores that factors dominate pangolin threats, as all eight are now listed as vulnerable to by the IUCN, with declines of 50-80% in trafficked regions unattributable to natural predation alone, which ecosystems historically buffered through reproductive rates of one offspring per year. In contrast, natural risks persist at sustainable levels in protected areas devoid of human interference, highlighting causal primacy of human activities in current extirpations.

Conservation Efforts

International Agreements and Listings

All eight species of pangolin (Manis spp.) were transferred from Appendix II to Appendix I of the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES) at the 17th Conference of the Parties (CoP17) held in , , from September 24 to October 5, 2016. This uplisting, which entered into force on January 2, 2017, prohibits international commercial in pangolins and their parts, aiming to curb the primary threat of driven by demand for scales and meat in and cuisine. Prior to this, the species were regulated under Appendix II, which permitted trade with export quotas and documentation but proved insufficient to stem escalating trafficking volumes documented in seizure data from 2000–2015. The CITES Appendix I designation requires range states to implement stricter domestic measures, including bans on exports and enhanced enforcement against illegal trade routes primarily linking to . However, compliance varies, with reports indicating continued large-scale seizures post-2017, such as over 100 tonnes of scales annually in some years, underscoring gaps in implementation despite the agreement's legal framework ratified by 184 parties. No other major multilateral environmental agreements, such as the Convention on Migratory Species (), specifically list or protect pangolins, as their primarily terrestrial, non-migratory habits fall outside CMS scope. On the International Union for Conservation of Nature ( of , all eight pangolin are classified as threatened, with four (Chinese, Sunda, Philippine, and tree pangolins) as , two (giant and Indian) as Endangered, and two African (white-bellied and black-bellied) as Vulnerable, reflecting declines of 50–80% over three generations due to overexploitation. These assessments, updated as recently as 2019, inform decisions but lack binding enforcement mechanisms, relying instead on voluntary national actions.

National and Local Initiatives

In China, pangolins received national first-class protected status under wildlife laws on June 3, 2020, prohibiting commercial trade and imposing severe penalties for violations, though enforcement challenges persist amid ongoing domestic demand for scales in traditional medicine. In January 2025, authorities announced an annual quota of 1 metric ton of pangolin scales for medicinal use, prompting criticism from conservation groups for potentially legitimizing sourcing that could fuel illegal imports despite international bans. India's Wildlife Protection Act of 1972 lists the Indian pangolin (Manis crassicaudata) under Schedule I, affording it the highest level of legal protection against hunting and trade, with recent national efforts including radio-collaring for population monitoring and deployment of detection dogs in collaboration with state forest departments since 2022. In Nigeria, the Endangered Species Act aligns with CITES to ban pangolin exploitation, supported by government actions such as the destruction of over 4 tonnes of seized pangolin scales and skins on October 16, 2023, as part of broader anti-trafficking measures. Local initiatives in emphasize rehabilitation and community involvement. In , the African Pangolin Working Group, established as a non-profit, coordinates species-specific , operations, and public across the continent's four pangolin , including partnerships for protection and anti-poaching training. Pangolin.Africa, based in the country, operates rehabilitation centers prioritizing swift release of rescued individuals into natural s while engaging local communities in monitoring and awareness programs to reduce poaching incentives. In , The Pangolin Project focuses on the Nyekweri Forest ecosystem, implementing community-driven patrols and nature-based financing to safeguard giant pangolins ( gigantea) across 25,000 acres, with efforts intensified since 2020 to counter encroachment. Nigeria's Pangolin Conservation Guild undertakes site-specific and awareness campaigns in high-trafficking regions, collaborating with locals for , such as the 2024 rehabilitation and release of white-bellied pangolins ( tricuspis) in . In , the Pangolin Conservation Project, launched with the Uganda Wildlife Authority, represents the country's first dedicated effort, funding patrols and capacity-building in key ranges to address hotspots. These grassroots programs often integrate economic alternatives for communities, such as tracking safaris in South Africa's Kalahari region, where participants contribute to data collection on Temminck's ground pangolins (Smutsia temminckii). Despite such targeted actions, data from seizures indicate that local enforcement gaps allow trafficking networks to persist, underscoring the need for sustained funding and inter-agency coordination.

Effectiveness and Data Gaps

Despite the uplisting of all eight pangolin species to Appendix I in , which prohibits commercial , illegal trafficking persists at levels insufficient to halt population declines, with the Pangolin Specialist Group reporting in September 2025 that species remain at high extinction risk due to overexploitation and habitat issues. Seizure data from indicate a reduction in detected pangolin equivalents from 3,000–4,000 annually in 2011–2012 to 400–600 in 2021–2022, suggesting partial deterrence from enhanced protections, though underreporting or shifts to undetected routes may confound assessments. National initiatives, such as China's legal and habitat improvements reported to in 2023, have strengthened enforcement in some areas, yet weak regional coordination and domestic demand sustain pressures. Local efforts like Operation Pangolin, launched in 2023, aim to bolster anti-trafficking and sustainable management but lack long-term outcome metrics as of 2025. Evaluating overall effectiveness is hindered by inconsistent enforcement and limited community engagement, with studies in identifying these as primary barriers to reducing risks. While resolutions since 2017 advocate increased funding and political commitment, implementation varies, contributing to ongoing extirpations in surveyed African populations over the past two decades. China's 2025 quota of 1 metric ton of pangolin scales for , purportedly from captive sources, has raised concerns over verification and potential laundering of wild specimens, underscoring gaps in oversight. Critical data gaps exacerbate these challenges, including unreliable population estimates due to pangolins' elusive, nocturnal habits and low densities, which render camera traps and line transects ineffective for monitoring. Reporting inconsistencies across range states, with 15 countries lacking any pangolin-specific , impede , as noted in IUCN assessments from August . Genetic studies reveal low diversity from historical declines, but baseline demographic data pre- and post-2017 protections remain sparse, complicating attribution of changes to actions versus natural variability. Targeted research on monitoring protocols is ongoing, yet opportunistic surveys dominate, yielding biased or incomplete insights into habitat-specific trends.

Recent Developments

Trade Seizure Trends Post-2020

Global seizures of pangolin scales and other products declined markedly after the 2019 peak of nearly 100 metric tons, dropping to approximately 20 metric tons in 2020 amid COVID-19-related border closures and logistical disruptions that hindered transnational smuggling networks. This post-pandemic reduction persisted through 2024, with large-scale seizures in that year registering 84% below 2019 levels, reflecting sustained lower volumes rather than merely improved concealment by traffickers. Analyses attribute the trend partly to pandemic-induced interruptions in source countries like and transit hubs in , alongside incremental gains in coordination, though seizure data inherently underestimates total illicit volumes due to undetected shipments. From 2015 to 2024, authorities documented seizures totaling about 181 metric tons of pangolin scales globally, with the post-2020 period accounting for a disproportionately smaller share compared to the pre-pandemic surge driven by demand in and . -monitored incidents from 2016 to 2024 encompassed 2,222 seizures equivalent to roughly 553,042 whole pangolins, but annual breakdowns indicate a tapering after 2020, with fewer high-volume interceptions in key routes from to . In the United States, for instance, pangolin specimen seizures from 2017 to 2023 numbered in the dozens, primarily scales originating from species, underscoring persistent but diminished inflows to consumer markets. Regional patterns reinforce the global downturn: African export seizures, which dominated pre-2020 trade, fell alongside reduced detections in Asian ports, while isolated upticks—such as heightened reporting in across nearly a third of districts—highlight localized persistence amid broader contraction. Enforcement bodies like the Wildlife Justice Commission note that while the slump signals disrupted networks, adaptive strategies by groups could mask ongoing pressures, necessitating expanded monitoring beyond seizures to gauge true trade dynamics. Into 2025, preliminary data suggest no rebound, with international reports emphasizing the role of fortified supply controls in source nations over demand-side interventions.

Policy Updates and Research Advances

![Destruction of confiscated pangolin scales in Cameroon by USFWS][float-right] In June 2025, the Fish and Wildlife Service proposed listing all seven Asian and African pangolin species as endangered under the Endangered Species Act, which would impose stricter domestic trade and import restrictions to combat ongoing trafficking. This move builds on Appendix I protections since 2017 but addresses persistent illegal trade documented in seizure data. In December 2024, established a national pangolin conservation expert committee to develop global strategies, amid vows to reduce medicinal use of scales. However, China's January 2025 announcement of a 1-metric-ton annual quota for pangolin scales in has drawn criticism from conservationists, who argue it undermines trade bans despite promises of gradual phase-out. Research efforts have advanced techniques, with a June 2025 study using GPS collars and accelerometers on five released s revealing nocturnal activity peaks and home ranges averaging 12.5 square kilometers, informing reintroduction protocols. Genetic analyses in January 2025 proposed a new species, indoburmanica, diverging from the around 3.4 million years ago, based on from Indian specimens, highlighting taxonomic complexities in conservation planning. An April 2025 application of developed a detection model achieving 95% accuracy on pangolin images from camera traps, enabling scalable in remote habitats. The IUCN Species Survival Commission Pangolin Specialist Group’s 2024-2025 report synthesizes data showing low across species due to , emphasizing the need for enhanced population surveys to fill reporting gaps identified in August 2025 assessments.

Ongoing Challenges in 2025

![Illicit wildlife market in Myanmar](./assets/Myanmar_Illicit_Endangered_Wildlife_Market_04_(cropped) In 2025, illegal trade remains a primary threat to all eight pangolin species, with seizures of scales and live specimens continuing despite CITES Appendix I listings prohibiting commercial trade. Operations in Nigeria, such as Operation Willow in March and Operation Orange in July, resulted in arrests of traffickers and confiscations of pangolin scales, underscoring persistent smuggling networks from Africa to Asia. A CITES-IUCN report highlighted that between 2016 and 2024, seizures involved over 100 metric tons of scales, equivalent to approximately 200,000 pangolins, though underreporting likely underestimates the scale. Habitat loss and fragmentation exacerbate poaching pressures, as for and reduces available and habitats across pangolin ranges in and . The U.S. Fish and Wildlife Service's June 2025 proposal to list seven pangolin species as endangered under the Endangered Species Act cited ongoing as a key factor contributing to projected population declines exceeding 50% in three generations for most species. Critical data gaps persist, with no comprehensive population surveys updated since pre-2020 assessments, impeding precise threat evaluation and conservation prioritization. The IUCN SSC Pangolin Specialist Group's September 2025 report emphasized that without improved monitoring and enforcement, overexploitation will continue driving species toward extinction, as current efforts fail to curb demand in consumer markets like China and Vietnam. Enforcement challenges, including corruption and limited resources in source countries, further hinder progress, as evidenced by ongoing detections of African pangolin derivatives in Asian seizures.